[
  {
    "path": ".gitignore",
    "content": ".idea"
  },
  {
    "path": "2325_nouns.json",
    "content": "[\r\n    \"aardvark\",\r\n    \"abyssinian\",\r\n    \"accelerator\",\r\n    \"accordion\",\r\n    \"account\",\r\n    \"accountant\",\r\n    \"acknowledgment\",\r\n    \"acoustic\",\r\n    \"acrylic\",\r\n    \"act\",\r\n    \"action\",\r\n    \"active\",\r\n    \"activity\",\r\n    \"actor\",\r\n    \"actress\",\r\n    \"adapter\",\r\n    \"addition\",\r\n    \"address\",\r\n    \"adjustment\",\r\n    \"adult\",\r\n    \"advantage\",\r\n    \"advertisement\",\r\n    \"advice\",\r\n    \"afghanistan\",\r\n    \"africa\",\r\n    \"aftermath\",\r\n    \"afternoon\",\r\n    \"aftershave\",\r\n    \"afterthought\",\r\n    \"age\",\r\n    \"agenda\",\r\n    \"agreement\",\r\n    \"air\",\r\n    \"airbus\",\r\n    \"airmail\",\r\n    \"airplane\",\r\n    \"airport\",\r\n    \"airship\",\r\n    \"alarm\",\r\n    \"albatross\",\r\n    \"alcohol\",\r\n    \"algebra\",\r\n    \"algeria\",\r\n    \"alibi\",\r\n    \"alley\",\r\n    \"alligator\",\r\n    \"alloy\",\r\n    \"almanac\",\r\n    \"alphabet\",\r\n    \"alto\",\r\n    \"aluminum\",\r\n    \"ambulance\",\r\n    \"america\",\r\n    \"amount\",\r\n    \"amusement\",\r\n    \"anatomy\",\r\n    \"anethesiologist\",\r\n    \"anger\",\r\n    \"angle\",\r\n    \"angora\",\r\n    \"animal\",\r\n    \"anime\",\r\n    \"ankle\",\r\n    \"answer\",\r\n    \"ant\",\r\n    \"antarctica\",\r\n    \"anteater\",\r\n    \"antelope\",\r\n    \"anthony\",\r\n    \"anthropology\",\r\n    \"apartment\",\r\n    \"apology\",\r\n    \"apparatus\",\r\n    \"apparel\",\r\n    \"appeal\",\r\n    \"appendix\",\r\n    \"apple\",\r\n    \"appliance\",\r\n    \"approval\",\r\n    \"april\",\r\n    \"aquarius\",\r\n    \"arch\",\r\n    \"archaeology\",\r\n    \"archeology\",\r\n    \"archer\",\r\n    \"architecture\",\r\n    \"area\",\r\n    \"argentina\",\r\n    \"argument\",\r\n    \"aries\",\r\n    \"arithmetic\",\r\n    \"arm\",\r\n    \"armadillo\",\r\n    \"armchair\",\r\n    \"armenian\",\r\n    \"army\",\r\n    \"arrow\",\r\n    \"art\",\r\n    \"ash\",\r\n    \"ashtray\",\r\n    \"asia\",\r\n    \"asparagus\",\r\n    \"asphalt\",\r\n    \"asterisk\",\r\n    \"astronomy\",\r\n    \"athlete\",\r\n    \"atm\",\r\n    \"atom\",\r\n    \"attack\",\r\n    \"attempt\",\r\n    \"attention\",\r\n    \"attic\",\r\n    \"attraction\",\r\n    \"august\",\r\n    \"aunt\",\r\n    \"australia\",\r\n    \"australian\",\r\n    \"author\",\r\n    \"authorisation\",\r\n    \"authority\",\r\n    \"authorization\",\r\n    \"avenue\",\r\n    \"babies\",\r\n    \"baboon\",\r\n    \"baby\",\r\n    \"back\",\r\n    \"backbone\",\r\n    \"bacon\",\r\n    \"badge\",\r\n    \"badger\",\r\n    \"bag\",\r\n    \"bagel\",\r\n    \"bagpipe\",\r\n    \"bail\",\r\n    \"bait\",\r\n    \"baker\",\r\n    \"bakery\",\r\n    \"balance\",\r\n    \"balinese\",\r\n    \"ball\",\r\n    \"balloon\",\r\n    \"bamboo\",\r\n    \"banana\",\r\n    \"band\",\r\n    \"bandana\",\r\n    \"bangladesh\",\r\n    \"bangle\",\r\n    \"banjo\",\r\n    \"bank\",\r\n    \"bankbook\",\r\n    \"banker\",\r\n    \"bar\",\r\n    \"barbara\",\r\n    \"barber\",\r\n    \"barge\",\r\n    \"baritone\",\r\n    \"barometer\",\r\n    \"base\",\r\n    \"baseball\",\r\n    \"basement\",\r\n    \"basin\",\r\n    \"basket\",\r\n    \"basketball\",\r\n    \"bass\",\r\n    \"bassoon\",\r\n    \"bat\",\r\n    \"bath\",\r\n    \"bathroom\",\r\n    \"bathtub\",\r\n    \"battery\",\r\n    \"battle\",\r\n    \"bay\",\r\n    \"beach\",\r\n    \"bead\",\r\n    \"beam\",\r\n    \"bean\",\r\n    \"bear\",\r\n    \"beard\",\r\n    \"beast\",\r\n    \"beat\",\r\n    \"beautician\",\r\n    \"beauty\",\r\n    \"beaver\",\r\n    \"bed\",\r\n    \"bedroom\",\r\n    \"bee\",\r\n    \"beech\",\r\n    \"beef\",\r\n    \"beer\",\r\n    \"beet\",\r\n    \"beetle\",\r\n    \"beggar\",\r\n    \"beginner\",\r\n    \"begonia\",\r\n    \"behavior\",\r\n    \"belgian\",\r\n    \"belief\",\r\n    \"believe\",\r\n    \"bell\",\r\n    \"belt\",\r\n    \"bench\",\r\n    \"bengal\",\r\n    \"beret\",\r\n    \"berry\",\r\n    \"bestseller\",\r\n    \"betty\",\r\n    \"bibliography\",\r\n    \"bicycle\",\r\n    \"bike\",\r\n    \"bill\",\r\n    \"billboard\",\r\n    \"biology\",\r\n    \"biplane\",\r\n    \"birch\",\r\n    \"bird\",\r\n    \"birth\",\r\n    \"birthday\",\r\n    \"bit\",\r\n    \"bite\",\r\n    \"black\",\r\n    \"bladder\",\r\n    \"blade\",\r\n    \"blanket\",\r\n    \"blinker\",\r\n    \"blizzard\",\r\n    \"block\",\r\n    \"blood\",\r\n    \"blouse\",\r\n    \"blow\",\r\n    \"blowgun\",\r\n    \"blue\",\r\n    \"board\",\r\n    \"boat\",\r\n    \"bobcat\",\r\n    \"body\",\r\n    \"bolt\",\r\n    \"bomb\",\r\n    \"bomber\",\r\n    \"bone\",\r\n    \"bongo\",\r\n    \"bonsai\",\r\n    \"book\",\r\n    \"bookcase\",\r\n    \"booklet\",\r\n    \"boot\",\r\n    \"border\",\r\n    \"botany\",\r\n    \"bottle\",\r\n    \"bottom\",\r\n    \"boundary\",\r\n    \"bow\",\r\n    \"bowl\",\r\n    \"bowling\",\r\n    \"box\",\r\n    \"boy\",\r\n    \"bra\",\r\n    \"brace\",\r\n    \"bracket\",\r\n    \"brain\",\r\n    \"brake\",\r\n    \"branch\",\r\n    \"brand\",\r\n    \"brandy\",\r\n    \"brass\",\r\n    \"brazil\",\r\n    \"bread\",\r\n    \"break\",\r\n    \"breakfast\",\r\n    \"breath\",\r\n    \"brian\",\r\n    \"brick\",\r\n    \"bridge\",\r\n    \"british\",\r\n    \"broccoli\",\r\n    \"brochure\",\r\n    \"broker\",\r\n    \"bronze\",\r\n    \"brother\",\r\n    \"brother-in-law\",\r\n    \"brow\",\r\n    \"brown\",\r\n    \"brush\",\r\n    \"bubble\",\r\n    \"bucket\",\r\n    \"budget\",\r\n    \"buffer\",\r\n    \"buffet\",\r\n    \"bugle\",\r\n    \"building\",\r\n    \"bulb\",\r\n    \"bull\",\r\n    \"bulldozer\",\r\n    \"bumper\",\r\n    \"bun\",\r\n    \"burglar\",\r\n    \"burma\",\r\n    \"burn\",\r\n    \"burst\",\r\n    \"bus\",\r\n    \"bush\",\r\n    \"business\",\r\n    \"butane\",\r\n    \"butcher\",\r\n    \"butter\",\r\n    \"button\",\r\n    \"buzzard\",\r\n    \"cabbage\",\r\n    \"cabinet\",\r\n    \"cable\",\r\n    \"cactus\",\r\n    \"cafe\",\r\n    \"cake\",\r\n    \"calculator\",\r\n    \"calculus\",\r\n    \"calendar\",\r\n    \"calf\",\r\n    \"call\",\r\n    \"camel\",\r\n    \"camera\",\r\n    \"camp\",\r\n    \"can\",\r\n    \"canada\",\r\n    \"canadian\",\r\n    \"cancer\",\r\n    \"candle\",\r\n    \"cannon\",\r\n    \"canoe\",\r\n    \"canvas\",\r\n    \"cap\",\r\n    \"capital\",\r\n    \"cappelletti\",\r\n    \"capricorn\",\r\n    \"captain\",\r\n    \"caption\",\r\n    \"car\",\r\n    \"caravan\",\r\n    \"card\",\r\n    \"cardboard\",\r\n    \"cardigan\",\r\n    \"care\",\r\n    \"carnation\",\r\n    \"carol\",\r\n    \"carp\",\r\n    \"carpenter\",\r\n    \"carriage\",\r\n    \"carrot\",\r\n    \"cart\",\r\n    \"cartoon\",\r\n    \"case\",\r\n    \"cast\",\r\n    \"castanet\",\r\n    \"cat\",\r\n    \"catamaran\",\r\n    \"caterpillar\",\r\n    \"cathedral\",\r\n    \"catsup\",\r\n    \"cattle\",\r\n    \"cauliflower\",\r\n    \"cause\",\r\n    \"caution\",\r\n    \"cave\",\r\n    \"c-clamp\",\r\n    \"cd\",\r\n    \"ceiling\",\r\n    \"celery\",\r\n    \"celeste\",\r\n    \"cell\",\r\n    \"cellar\",\r\n    \"cello\",\r\n    \"celsius\",\r\n    \"cement\",\r\n    \"cemetery\",\r\n    \"cent\",\r\n    \"centimeter\",\r\n    \"century\",\r\n    \"ceramic\",\r\n    \"cereal\",\r\n    \"certification\",\r\n    \"chain\",\r\n    \"chair\",\r\n    \"chalk\",\r\n    \"chance\",\r\n    \"change\",\r\n    \"channel\",\r\n    \"character\",\r\n    \"chard\",\r\n    \"charles\",\r\n    \"chauffeur\",\r\n    \"check\",\r\n    \"cheek\",\r\n    \"cheese\",\r\n    \"cheetah\",\r\n    \"chef\",\r\n    \"chemistry\",\r\n    \"cheque\",\r\n    \"cherries\",\r\n    \"cherry\",\r\n    \"chess\",\r\n    \"chest\",\r\n    \"chick\",\r\n    \"chicken\",\r\n    \"chicory\",\r\n    \"chief\",\r\n    \"child\",\r\n    \"children\",\r\n    \"chill\",\r\n    \"chime\",\r\n    \"chimpanzee\",\r\n    \"chin\",\r\n    \"china\",\r\n    \"chinese\",\r\n    \"chive\",\r\n    \"chocolate\",\r\n    \"chord\",\r\n    \"christmas\",\r\n    \"christopher\",\r\n    \"chronometer\",\r\n    \"church\",\r\n    \"cicada\",\r\n    \"cinema\",\r\n    \"circle\",\r\n    \"circulation\",\r\n    \"cirrus\",\r\n    \"citizenship\",\r\n    \"city\",\r\n    \"clam\",\r\n    \"clarinet\",\r\n    \"class\",\r\n    \"claus\",\r\n    \"clave\",\r\n    \"clef\",\r\n    \"clerk\",\r\n    \"click\",\r\n    \"client\",\r\n    \"climb\",\r\n    \"clipper\",\r\n    \"cloakroom\",\r\n    \"clock\",\r\n    \"close\",\r\n    \"closet\",\r\n    \"cloth\",\r\n    \"cloud\",\r\n    \"cloudy\",\r\n    \"clover\",\r\n    \"club\",\r\n    \"clutch\",\r\n    \"coach\",\r\n    \"coal\",\r\n    \"coast\",\r\n    \"coat\",\r\n    \"cobweb\",\r\n    \"cockroach\",\r\n    \"cocktail\",\r\n    \"cocoa\",\r\n    \"cod\",\r\n    \"coffee\",\r\n    \"coil\",\r\n    \"coin\",\r\n    \"coke\",\r\n    \"cold\",\r\n    \"collar\",\r\n    \"college\",\r\n    \"collision\",\r\n    \"colombia\",\r\n    \"colon\",\r\n    \"colony\",\r\n    \"color\",\r\n    \"colt\",\r\n    \"column\",\r\n    \"columnist\",\r\n    \"comb\",\r\n    \"comfort\",\r\n    \"comic\",\r\n    \"comma\",\r\n    \"command\",\r\n    \"commission\",\r\n    \"committee\",\r\n    \"community\",\r\n    \"company\",\r\n    \"comparison\",\r\n    \"competition\",\r\n    \"competitor\",\r\n    \"composer\",\r\n    \"composition\",\r\n    \"computer\",\r\n    \"condition\",\r\n    \"condor\",\r\n    \"cone\",\r\n    \"confirmation\",\r\n    \"conga\",\r\n    \"congo\",\r\n    \"conifer\",\r\n    \"connection\",\r\n    \"consonant\",\r\n    \"continent\",\r\n    \"control\",\r\n    \"cook\",\r\n    \"cooking\",\r\n    \"copy\",\r\n    \"copyright\",\r\n    \"cord\",\r\n    \"cork\",\r\n    \"cormorant\",\r\n    \"corn\",\r\n    \"cornet\",\r\n    \"correspondent\",\r\n    \"cost\",\r\n    \"cotton\",\r\n    \"couch\",\r\n    \"cougar\",\r\n    \"cough\",\r\n    \"country\",\r\n    \"course\",\r\n    \"court\",\r\n    \"cousin\",\r\n    \"cover\",\r\n    \"cow\",\r\n    \"cowbell\",\r\n    \"crab\",\r\n    \"crack\",\r\n    \"cracker\",\r\n    \"craftsman\",\r\n    \"crate\",\r\n    \"crawdad\",\r\n    \"crayfish\",\r\n    \"crayon\",\r\n    \"cream\",\r\n    \"creator\",\r\n    \"creature\",\r\n    \"credit\",\r\n    \"creditor\",\r\n    \"creek\",\r\n    \"crib\",\r\n    \"cricket\",\r\n    \"crime\",\r\n    \"criminal\",\r\n    \"crocodile\",\r\n    \"crocus\",\r\n    \"croissant\",\r\n    \"crook\",\r\n    \"crop\",\r\n    \"cross\",\r\n    \"crow\",\r\n    \"crowd\",\r\n    \"crown\",\r\n    \"crush\",\r\n    \"cry\",\r\n    \"cub\",\r\n    \"cuban\",\r\n    \"cucumber\",\r\n    \"cultivator\",\r\n    \"cup\",\r\n    \"cupboard\",\r\n    \"cupcake\",\r\n    \"curler\",\r\n    \"currency\",\r\n    \"current\",\r\n    \"curtain\",\r\n    \"curve\",\r\n    \"cushion\",\r\n    \"custard\",\r\n    \"customer\",\r\n    \"cut\",\r\n    \"cuticle\",\r\n    \"cycle\",\r\n    \"cyclone\",\r\n    \"cylinder\",\r\n    \"cymbal\",\r\n    \"dad\",\r\n    \"daffodil\",\r\n    \"dahlia\",\r\n    \"daisy\",\r\n    \"damage\",\r\n    \"dance\",\r\n    \"dancer\",\r\n    \"danger\",\r\n    \"daniel\",\r\n    \"dash\",\r\n    \"dashboard\",\r\n    \"database\",\r\n    \"date\",\r\n    \"daughter\",\r\n    \"david\",\r\n    \"day\",\r\n    \"dead\",\r\n    \"deadline\",\r\n    \"deal\",\r\n    \"death\",\r\n    \"deborah\",\r\n    \"debt\",\r\n    \"debtor\",\r\n    \"decade\",\r\n    \"december\",\r\n    \"decimal\",\r\n    \"decision\",\r\n    \"decrease\",\r\n    \"dedication\",\r\n    \"deer\",\r\n    \"defense\",\r\n    \"deficit\",\r\n    \"degree\",\r\n    \"delete\",\r\n    \"delivery\",\r\n    \"den\",\r\n    \"denim\",\r\n    \"dentist\",\r\n    \"deodorant\",\r\n    \"department\",\r\n    \"deposit\",\r\n    \"description\",\r\n    \"desert\",\r\n    \"design\",\r\n    \"desire\",\r\n    \"desk\",\r\n    \"dessert\",\r\n    \"destruction\",\r\n    \"detail\",\r\n    \"detective\",\r\n    \"development\",\r\n    \"dew\",\r\n    \"diamond\",\r\n    \"diaphragm\",\r\n    \"dibble\",\r\n    \"dictionary\",\r\n    \"dietician\",\r\n    \"difference\",\r\n    \"digestion\",\r\n    \"digger\",\r\n    \"digital\",\r\n    \"dill\",\r\n    \"dime\",\r\n    \"dimple\",\r\n    \"dinghy\",\r\n    \"dinner\",\r\n    \"dinosaur\",\r\n    \"diploma\",\r\n    \"dipstick\",\r\n    \"direction\",\r\n    \"dirt\",\r\n    \"disadvantage\",\r\n    \"discovery\",\r\n    \"discussion\",\r\n    \"disease\",\r\n    \"disgust\",\r\n    \"dish\",\r\n    \"distance\",\r\n    \"distribution\",\r\n    \"distributor\",\r\n    \"diving\",\r\n    \"division\",\r\n    \"divorced\",\r\n    \"dock\",\r\n    \"doctor\",\r\n    \"dog\",\r\n    \"dogsled\",\r\n    \"doll\",\r\n    \"dollar\",\r\n    \"dolphin\",\r\n    \"domain\",\r\n    \"donald\",\r\n    \"donkey\",\r\n    \"donna\",\r\n    \"door\",\r\n    \"dorothy\",\r\n    \"double\",\r\n    \"doubt\",\r\n    \"downtown\",\r\n    \"dragon\",\r\n    \"dragonfly\",\r\n    \"drain\",\r\n    \"drake\",\r\n    \"drama\",\r\n    \"draw\",\r\n    \"drawbridge\",\r\n    \"drawer\",\r\n    \"dream\",\r\n    \"dredger\",\r\n    \"dress\",\r\n    \"dresser\",\r\n    \"dressing\",\r\n    \"drill\",\r\n    \"drink\",\r\n    \"drive\",\r\n    \"driver\",\r\n    \"driving\",\r\n    \"drizzle\",\r\n    \"drop\",\r\n    \"drug\",\r\n    \"drum\",\r\n    \"dry\",\r\n    \"dryer\",\r\n    \"duck\",\r\n    \"duckling\",\r\n    \"dugout\",\r\n    \"dungeon\",\r\n    \"dust\",\r\n    \"eagle\",\r\n    \"ear\",\r\n    \"earth\",\r\n    \"earthquake\",\r\n    \"ease\",\r\n    \"east\",\r\n    \"edge\",\r\n    \"edger\",\r\n    \"editor\",\r\n    \"editorial\",\r\n    \"education\",\r\n    \"edward\",\r\n    \"eel\",\r\n    \"effect\",\r\n    \"egg\",\r\n    \"eggnog\",\r\n    \"eggplant\",\r\n    \"egypt\",\r\n    \"eight\",\r\n    \"elbow\",\r\n    \"element\",\r\n    \"elephant\",\r\n    \"elizabeth\",\r\n    \"ellipse\",\r\n    \"emery\",\r\n    \"employee\",\r\n    \"employer\",\r\n    \"encyclopedia\",\r\n    \"end\",\r\n    \"enemy\",\r\n    \"energy\",\r\n    \"engine\",\r\n    \"engineer\",\r\n    \"engineering\",\r\n    \"english\",\r\n    \"enquiry\",\r\n    \"entrance\",\r\n    \"environment\",\r\n    \"epoch\",\r\n    \"epoxy\",\r\n    \"equinox\",\r\n    \"equipment\",\r\n    \"era\",\r\n    \"error\",\r\n    \"estimate\",\r\n    \"ethernet\",\r\n    \"ethiopia\",\r\n    \"euphonium\",\r\n    \"europe\",\r\n    \"evening\",\r\n    \"event\",\r\n    \"examination\",\r\n    \"example\",\r\n    \"exchange\",\r\n    \"exclamation\",\r\n    \"exhaust\",\r\n    \"ex-husband\",\r\n    \"existence\",\r\n    \"expansion\",\r\n    \"experience\",\r\n    \"expert\",\r\n    \"explanation\",\r\n    \"ex-wife\",\r\n    \"eye\",\r\n    \"eyebrow\",\r\n    \"eyelash\",\r\n    \"eyeliner\",\r\n    \"face\",\r\n    \"facilities\",\r\n    \"fact\",\r\n    \"factory\",\r\n    \"fahrenheit\",\r\n    \"fairies\",\r\n    \"fall\",\r\n    \"family\",\r\n    \"fan\",\r\n    \"fang\",\r\n    \"farm\",\r\n    \"farmer\",\r\n    \"fat\",\r\n    \"father\",\r\n    \"father-in-law\",\r\n    \"faucet\",\r\n    \"fear\",\r\n    \"feast\",\r\n    \"feather\",\r\n    \"feature\",\r\n    \"february\",\r\n    \"fedelini\",\r\n    \"feedback\",\r\n    \"feeling\",\r\n    \"feet\",\r\n    \"felony\",\r\n    \"female\",\r\n    \"fender\",\r\n    \"ferry\",\r\n    \"ferryboat\",\r\n    \"fertilizer\",\r\n    \"fiber\",\r\n    \"fiberglass\",\r\n    \"fibre\",\r\n    \"fiction\",\r\n    \"field\",\r\n    \"fifth\",\r\n    \"fight\",\r\n    \"fighter\",\r\n    \"file\",\r\n    \"find\",\r\n    \"fine\",\r\n    \"finger\",\r\n    \"fir\",\r\n    \"fire\",\r\n    \"fired\",\r\n    \"fireman\",\r\n    \"fireplace\",\r\n    \"firewall\",\r\n    \"fish\",\r\n    \"fisherman\",\r\n    \"flag\",\r\n    \"flame\",\r\n    \"flare\",\r\n    \"flat\",\r\n    \"flavor\",\r\n    \"flax\",\r\n    \"flesh\",\r\n    \"flight\",\r\n    \"flock\",\r\n    \"flood\",\r\n    \"floor\",\r\n    \"flower\",\r\n    \"flugelhorn\",\r\n    \"flute\",\r\n    \"fly\",\r\n    \"foam\",\r\n    \"fog\",\r\n    \"fold\",\r\n    \"font\",\r\n    \"food\",\r\n    \"foot\",\r\n    \"football\",\r\n    \"footnote\",\r\n    \"force\",\r\n    \"forecast\",\r\n    \"forehead\",\r\n    \"forest\",\r\n    \"forgery\",\r\n    \"fork\",\r\n    \"form\",\r\n    \"format\",\r\n    \"fortnight\",\r\n    \"foundation\",\r\n    \"fountain\",\r\n    \"fowl\",\r\n    \"fox\",\r\n    \"foxglove\",\r\n    \"fragrance\",\r\n    \"frame\",\r\n    \"france\",\r\n    \"freckle\",\r\n    \"freeze\",\r\n    \"freezer\",\r\n    \"freighter\",\r\n    \"french\",\r\n    \"freon\",\r\n    \"friction\",\r\n    \"friday\",\r\n    \"fridge\",\r\n    \"friend\",\r\n    \"frog\",\r\n    \"front\",\r\n    \"frost\",\r\n    \"frown\",\r\n    \"fruit\",\r\n    \"fuel\",\r\n    \"fur\",\r\n    \"furniture\",\r\n    \"galley\",\r\n    \"gallon\",\r\n    \"game\",\r\n    \"gander\",\r\n    \"garage\",\r\n    \"garden\",\r\n    \"garlic\",\r\n    \"gas\",\r\n    \"gasoline\",\r\n    \"gate\",\r\n    \"gateway\",\r\n    \"gauge\",\r\n    \"gazelle\",\r\n    \"gear\",\r\n    \"gearshift\",\r\n    \"geese\",\r\n    \"gemini\",\r\n    \"gender\",\r\n    \"geography\",\r\n    \"geology\",\r\n    \"geometry\",\r\n    \"george\",\r\n    \"geranium\",\r\n    \"german\",\r\n    \"germany\",\r\n    \"ghana\",\r\n    \"ghost\",\r\n    \"giant\",\r\n    \"giraffe\",\r\n    \"girdle\",\r\n    \"girl\",\r\n    \"gladiolus\",\r\n    \"glass\",\r\n    \"glider\",\r\n    \"gliding\",\r\n    \"glockenspiel\",\r\n    \"glove\",\r\n    \"glue\",\r\n    \"goal\",\r\n    \"goat\",\r\n    \"goldfish\",\r\n    \"golf\",\r\n    \"gondola\",\r\n    \"gong\",\r\n    \"good-bye\",\r\n    \"goose\",\r\n    \"gore-tex\",\r\n    \"gorilla\",\r\n    \"gosling\",\r\n    \"government\",\r\n    \"governor\",\r\n    \"grade\",\r\n    \"grain\",\r\n    \"gram\",\r\n    \"granddaughter\",\r\n    \"grandfather\",\r\n    \"grandmother\",\r\n    \"grandson\",\r\n    \"grape\",\r\n    \"graphic\",\r\n    \"grass\",\r\n    \"grasshopper\",\r\n    \"gray\",\r\n    \"grease\",\r\n    \"great-grandfather\",\r\n    \"great-grandmother\",\r\n    \"greece\",\r\n    \"greek\",\r\n    \"green\",\r\n    \"grenade\",\r\n    \"grey\",\r\n    \"grill\",\r\n    \"grip\",\r\n    \"ground\",\r\n    \"group\",\r\n    \"grouse\",\r\n    \"growth\",\r\n    \"guarantee\",\r\n    \"guatemalan\",\r\n    \"guide\",\r\n    \"guilty\",\r\n    \"guitar\",\r\n    \"gum\",\r\n    \"gun\",\r\n    \"gym\",\r\n    \"gymnast\",\r\n    \"hacksaw\",\r\n    \"hail\",\r\n    \"hair\",\r\n    \"haircut\",\r\n    \"half-brother\",\r\n    \"half-sister\",\r\n    \"halibut\",\r\n    \"hall\",\r\n    \"hallway\",\r\n    \"hamburger\",\r\n    \"hammer\",\r\n    \"hamster\",\r\n    \"hand\",\r\n    \"handball\",\r\n    \"handicap\",\r\n    \"handle\",\r\n    \"handsaw\",\r\n    \"harbor\",\r\n    \"hardboard\",\r\n    \"hardcover\",\r\n    \"hardhat\",\r\n    \"hardware\",\r\n    \"harmonica\",\r\n    \"harmony\",\r\n    \"harp\",\r\n    \"hat\",\r\n    \"hate\",\r\n    \"hawk\",\r\n    \"head\",\r\n    \"headlight\",\r\n    \"headline\",\r\n    \"health\",\r\n    \"hearing\",\r\n    \"heart\",\r\n    \"heat\",\r\n    \"heaven\",\r\n    \"hedge\",\r\n    \"height\",\r\n    \"helen\",\r\n    \"helicopter\",\r\n    \"hell\",\r\n    \"helmet\",\r\n    \"help\",\r\n    \"hemp\",\r\n    \"hen\",\r\n    \"heron\",\r\n    \"herring\",\r\n    \"hexagon\",\r\n    \"hill\",\r\n    \"himalayan\",\r\n    \"hip\",\r\n    \"hippopotamus\",\r\n    \"history\",\r\n    \"hobbies\",\r\n    \"hockey\",\r\n    \"hoe\",\r\n    \"hole\",\r\n    \"holiday\",\r\n    \"home\",\r\n    \"honey\",\r\n    \"hood\",\r\n    \"hook\",\r\n    \"hope\",\r\n    \"horn\",\r\n    \"horse\",\r\n    \"hose\",\r\n    \"hospital\",\r\n    \"hot\",\r\n    \"hour\",\r\n    \"hourglass\",\r\n    \"house\",\r\n    \"hovercraft\",\r\n    \"hub\",\r\n    \"hubcap\",\r\n    \"humidity\",\r\n    \"humor\",\r\n    \"hurricane\",\r\n    \"hyacinth\",\r\n    \"hydrant\",\r\n    \"hydrofoil\",\r\n    \"hyena\",\r\n    \"hygienic\",\r\n    \"ice\",\r\n    \"icebreaker\",\r\n    \"icicle\",\r\n    \"icon\",\r\n    \"idea\",\r\n    \"ikebana\",\r\n    \"illegal\",\r\n    \"imprisonment\",\r\n    \"improvement\",\r\n    \"impulse\",\r\n    \"inch\",\r\n    \"income\",\r\n    \"increase\",\r\n    \"index\",\r\n    \"india\",\r\n    \"indonesia\",\r\n    \"industry\",\r\n    \"ink\",\r\n    \"innocent\",\r\n    \"input\",\r\n    \"insect\",\r\n    \"instruction\",\r\n    \"instrument\",\r\n    \"insulation\",\r\n    \"insurance\",\r\n    \"interactive\",\r\n    \"interest\",\r\n    \"internet\",\r\n    \"interviewer\",\r\n    \"intestine\",\r\n    \"invention\",\r\n    \"inventory\",\r\n    \"invoice\",\r\n    \"iran\",\r\n    \"iraq\",\r\n    \"iris\",\r\n    \"island\",\r\n    \"israel\",\r\n    \"italian\",\r\n    \"italy\",\r\n    \"jacket\",\r\n    \"jaguar\",\r\n    \"jail\",\r\n    \"jam\",\r\n    \"james\",\r\n    \"january\",\r\n    \"japan\",\r\n    \"japanese\",\r\n    \"jar\",\r\n    \"jasmine\",\r\n    \"jason\",\r\n    \"jaw\",\r\n    \"jeans\",\r\n    \"jeep\",\r\n    \"jeff\",\r\n    \"jelly\",\r\n    \"jellyfish\",\r\n    \"jennifer\",\r\n    \"jet\",\r\n    \"jewel\",\r\n    \"jogging\",\r\n    \"john\",\r\n    \"join\",\r\n    \"joke\",\r\n    \"joseph\",\r\n    \"journey\",\r\n    \"judge\",\r\n    \"judo\",\r\n    \"juice\",\r\n    \"july\",\r\n    \"jumbo\",\r\n    \"jump\",\r\n    \"jumper\",\r\n    \"june\",\r\n    \"jury\",\r\n    \"justice\",\r\n    \"jute\",\r\n    \"kale\",\r\n    \"kamikaze\",\r\n    \"kangaroo\",\r\n    \"karate\",\r\n    \"karen\",\r\n    \"kayak\",\r\n    \"kendo\",\r\n    \"kenneth\",\r\n    \"kenya\",\r\n    \"ketchup\",\r\n    \"kettle\",\r\n    \"kettledrum\",\r\n    \"kevin\",\r\n    \"key\",\r\n    \"keyboard\",\r\n    \"keyboarding\",\r\n    \"kick\",\r\n    \"kidney\",\r\n    \"kilogram\",\r\n    \"kilometer\",\r\n    \"kimberly\",\r\n    \"kiss\",\r\n    \"kitchen\",\r\n    \"kite\",\r\n    \"kitten\",\r\n    \"kitty\",\r\n    \"knee\",\r\n    \"knickers\",\r\n    \"knife\",\r\n    \"knight\",\r\n    \"knot\",\r\n    \"knowledge\",\r\n    \"kohlrabi\",\r\n    \"korean\",\r\n    \"laborer\",\r\n    \"lace\",\r\n    \"ladybug\",\r\n    \"lake\",\r\n    \"lamb\",\r\n    \"lamp\",\r\n    \"lan\",\r\n    \"land\",\r\n    \"landmine\",\r\n    \"language\",\r\n    \"larch\",\r\n    \"lasagna\",\r\n    \"latency\",\r\n    \"latex\",\r\n    \"lathe\",\r\n    \"laugh\",\r\n    \"laundry\",\r\n    \"laura\",\r\n    \"law\",\r\n    \"lawyer\",\r\n    \"layer\",\r\n    \"leaf\",\r\n    \"learning\",\r\n    \"leather\",\r\n    \"leek\",\r\n    \"leg\",\r\n    \"legal\",\r\n    \"lemonade\",\r\n    \"lentil\",\r\n    \"leo\",\r\n    \"leopard\",\r\n    \"letter\",\r\n    \"lettuce\",\r\n    \"level\",\r\n    \"libra\",\r\n    \"library\",\r\n    \"license\",\r\n    \"lier\",\r\n    \"lift\",\r\n    \"light\",\r\n    \"lightning\",\r\n    \"lilac\",\r\n    \"lily\",\r\n    \"limit\",\r\n    \"linda\",\r\n    \"line\",\r\n    \"linen\",\r\n    \"link\",\r\n    \"lion\",\r\n    \"lip\",\r\n    \"lipstick\",\r\n    \"liquid\",\r\n    \"liquor\",\r\n    \"lisa\",\r\n    \"list\",\r\n    \"literature\",\r\n    \"litter\",\r\n    \"liver\",\r\n    \"lizard\",\r\n    \"llama\",\r\n    \"loaf\",\r\n    \"loan\",\r\n    \"lobster\",\r\n    \"lock\",\r\n    \"locket\",\r\n    \"locust\",\r\n    \"look\",\r\n    \"loss\",\r\n    \"lotion\",\r\n    \"love\",\r\n    \"low\",\r\n    \"lumber\",\r\n    \"lunch\",\r\n    \"lunchroom\",\r\n    \"lung\",\r\n    \"lunge\",\r\n    \"lute\",\r\n    \"luttuce\",\r\n    \"lycra\",\r\n    \"lynx\",\r\n    \"lyocell\",\r\n    \"lyre\",\r\n    \"lyric\",\r\n    \"macaroni\",\r\n    \"machine\",\r\n    \"macrame\",\r\n    \"magazine\",\r\n    \"magic\",\r\n    \"magician\",\r\n    \"maid\",\r\n    \"mail\",\r\n    \"mailbox\",\r\n    \"mailman\",\r\n    \"makeup\",\r\n    \"malaysia\",\r\n    \"male\",\r\n    \"mall\",\r\n    \"mallet\",\r\n    \"man\",\r\n    \"manager\",\r\n    \"mandolin\",\r\n    \"manicure\",\r\n    \"manx\",\r\n    \"map\",\r\n    \"maple\",\r\n    \"maraca\",\r\n    \"marble\",\r\n    \"march\",\r\n    \"margaret\",\r\n    \"margin\",\r\n    \"maria\",\r\n    \"marimba\",\r\n    \"mark\",\r\n    \"mark\",\r\n    \"market\",\r\n    \"married\",\r\n    \"mary\",\r\n    \"mascara\",\r\n    \"mask\",\r\n    \"mass\",\r\n    \"match\",\r\n    \"math\",\r\n    \"mattock\",\r\n    \"may\",\r\n    \"mayonnaise\",\r\n    \"meal\",\r\n    \"measure\",\r\n    \"meat\",\r\n    \"mechanic\",\r\n    \"medicine\",\r\n    \"meeting\",\r\n    \"melody\",\r\n    \"memory\",\r\n    \"men\",\r\n    \"menu\",\r\n    \"message\",\r\n    \"metal\",\r\n    \"meteorology\",\r\n    \"meter\",\r\n    \"methane\",\r\n    \"mexican\",\r\n    \"mexico\",\r\n    \"mice\",\r\n    \"michael\",\r\n    \"michelle\",\r\n    \"microwave\",\r\n    \"middle\",\r\n    \"mile\",\r\n    \"milk\",\r\n    \"milkshake\",\r\n    \"millennium\",\r\n    \"millimeter\",\r\n    \"millisecond\",\r\n    \"mimosa\",\r\n    \"mind\",\r\n    \"mine\",\r\n    \"minibus\",\r\n    \"mini-skirt\",\r\n    \"minister\",\r\n    \"mint\",\r\n    \"minute\",\r\n    \"mirror\",\r\n    \"missile\",\r\n    \"mist\",\r\n    \"mistake\",\r\n    \"mitten\",\r\n    \"moat\",\r\n    \"modem\",\r\n    \"mole\",\r\n    \"mom\",\r\n    \"monday\",\r\n    \"money\",\r\n    \"monkey\",\r\n    \"month\",\r\n    \"moon\",\r\n    \"morning\",\r\n    \"morocco\",\r\n    \"mosque\",\r\n    \"mosquito\",\r\n    \"mother\",\r\n    \"mother-in-law\",\r\n    \"motion\",\r\n    \"motorboat\",\r\n    \"motorcycle\",\r\n    \"mountain\",\r\n    \"mouse\",\r\n    \"moustache\",\r\n    \"mouth\",\r\n    \"move\",\r\n    \"multi-hop\",\r\n    \"multimedia\",\r\n    \"muscle\",\r\n    \"museum\",\r\n    \"music\",\r\n    \"musician\",\r\n    \"mustard\",\r\n    \"myanmar\",\r\n    \"nail\",\r\n    \"name\",\r\n    \"nancy\",\r\n    \"napkin\",\r\n    \"narcissus\",\r\n    \"nation\",\r\n    \"neck\",\r\n    \"need\",\r\n    \"needle\",\r\n    \"nepal\",\r\n    \"nephew\",\r\n    \"nerve\",\r\n    \"nest\",\r\n    \"net\",\r\n    \"network\",\r\n    \"news\",\r\n    \"newsprint\",\r\n    \"newsstand\",\r\n    \"nic\",\r\n    \"niece\",\r\n    \"nigeria\",\r\n    \"night\",\r\n    \"node\",\r\n    \"noise\",\r\n    \"noodle\",\r\n    \"north\",\r\n    \"north\",\r\n    \"america\",\r\n    \"north\",\r\n    \"korea\",\r\n    \"norwegian\",\r\n    \"nose\",\r\n    \"note\",\r\n    \"notebook\",\r\n    \"notify\",\r\n    \"novel\",\r\n    \"november\",\r\n    \"number\",\r\n    \"numeric\",\r\n    \"nurse\",\r\n    \"nut\",\r\n    \"nylon\",\r\n    \"oak\",\r\n    \"oatmeal\",\r\n    \"objective\",\r\n    \"oboe\",\r\n    \"observation\",\r\n    \"occupation\",\r\n    \"ocean\",\r\n    \"ocelot\",\r\n    \"octagon\",\r\n    \"octave\",\r\n    \"october\",\r\n    \"octopus\",\r\n    \"odometer\",\r\n    \"offence\",\r\n    \"offer\",\r\n    \"office\",\r\n    \"oil\",\r\n    \"okra\",\r\n    \"olive\",\r\n    \"onion\",\r\n    \"open\",\r\n    \"opera\",\r\n    \"operation\",\r\n    \"ophthalmologist\",\r\n    \"opinion\",\r\n    \"option\",\r\n    \"orange\",\r\n    \"orchestra\",\r\n    \"orchid\",\r\n    \"order\",\r\n    \"organ\",\r\n    \"organisation\",\r\n    \"organization\",\r\n    \"ornament\",\r\n    \"ostrich\",\r\n    \"otter\",\r\n    \"ounce\",\r\n    \"output\",\r\n    \"outrigger\",\r\n    \"oval\",\r\n    \"oven\",\r\n    \"overcoat\",\r\n    \"owl\",\r\n    \"owner\",\r\n    \"ox\",\r\n    \"oyster\",\r\n    \"package\",\r\n    \"packet\",\r\n    \"page\",\r\n    \"pail\",\r\n    \"pain\",\r\n    \"paint\",\r\n    \"pair\",\r\n    \"pajama\",\r\n    \"pakistan\",\r\n    \"palm\",\r\n    \"pamphlet\",\r\n    \"pan\",\r\n    \"pancake\",\r\n    \"pancreas\",\r\n    \"panda\",\r\n    \"pansy\",\r\n    \"panther\",\r\n    \"panties\",\r\n    \"pantry\",\r\n    \"pants\",\r\n    \"panty\",\r\n    \"pantyhose\",\r\n    \"paper\",\r\n    \"paperback\",\r\n    \"parade\",\r\n    \"parallelogram\",\r\n    \"parcel\",\r\n    \"parent\",\r\n    \"parentheses\",\r\n    \"park\",\r\n    \"parrot\",\r\n    \"parsnip\",\r\n    \"part\",\r\n    \"particle\",\r\n    \"partner\",\r\n    \"partridge\",\r\n    \"party\",\r\n    \"passbook\",\r\n    \"passenger\",\r\n    \"passive\",\r\n    \"pasta\",\r\n    \"paste\",\r\n    \"pastor\",\r\n    \"pastry\",\r\n    \"patch\",\r\n    \"path\",\r\n    \"patient\",\r\n    \"patio\",\r\n    \"patricia\",\r\n    \"paul\",\r\n    \"payment\",\r\n    \"pea\",\r\n    \"peace\",\r\n    \"peak\",\r\n    \"peanut\",\r\n    \"pear\",\r\n    \"pedestrian\",\r\n    \"pediatrician\",\r\n    \"peen\",\r\n    \"peer-to-peer\",\r\n    \"pelican\",\r\n    \"pen\",\r\n    \"penalty\",\r\n    \"pencil\",\r\n    \"pendulum\",\r\n    \"pentagon\",\r\n    \"peony\",\r\n    \"pepper\",\r\n    \"perch\",\r\n    \"perfume\",\r\n    \"period\",\r\n    \"periodical\",\r\n    \"peripheral\",\r\n    \"permission\",\r\n    \"persian\",\r\n    \"person\",\r\n    \"peru\",\r\n    \"pest\",\r\n    \"pet\",\r\n    \"pharmacist\",\r\n    \"pheasant\",\r\n    \"philippines\",\r\n    \"philosophy\",\r\n    \"phone\",\r\n    \"physician\",\r\n    \"piano\",\r\n    \"piccolo\",\r\n    \"pickle\",\r\n    \"picture\",\r\n    \"pie\",\r\n    \"pig\",\r\n    \"pigeon\",\r\n    \"pike\",\r\n    \"pillow\",\r\n    \"pilot\",\r\n    \"pimple\",\r\n    \"pin\",\r\n    \"pine\",\r\n    \"ping\",\r\n    \"pink\",\r\n    \"pint\",\r\n    \"pipe\",\r\n    \"pisces\",\r\n    \"pizza\",\r\n    \"place\",\r\n    \"plain\",\r\n    \"plane\",\r\n    \"planet\",\r\n    \"plant\",\r\n    \"plantation\",\r\n    \"plaster\",\r\n    \"plasterboard\",\r\n    \"plastic\",\r\n    \"plate\",\r\n    \"play\",\r\n    \"playground\",\r\n    \"playroom\",\r\n    \"pleasure\",\r\n    \"plier\",\r\n    \"plot\",\r\n    \"plough\",\r\n    \"plow\",\r\n    \"plywood\",\r\n    \"pocket\",\r\n    \"poet\",\r\n    \"point\",\r\n    \"poison\",\r\n    \"poland\",\r\n    \"police\",\r\n    \"policeman\",\r\n    \"polish\",\r\n    \"politician\",\r\n    \"pollution\",\r\n    \"polo\",\r\n    \"polyester\",\r\n    \"pond\",\r\n    \"popcorn\",\r\n    \"poppy\",\r\n    \"population\",\r\n    \"porch\",\r\n    \"porcupine\",\r\n    \"port\",\r\n    \"porter\",\r\n    \"position\",\r\n    \"possibility\",\r\n    \"postage\",\r\n    \"postbox\",\r\n    \"pot\",\r\n    \"potato\",\r\n    \"poultry\",\r\n    \"pound\",\r\n    \"powder\",\r\n    \"power\",\r\n    \"precipitation\",\r\n    \"preface\",\r\n    \"prepared\",\r\n    \"pressure\",\r\n    \"price\",\r\n    \"priest\",\r\n    \"print\",\r\n    \"printer\",\r\n    \"prison\",\r\n    \"probation\",\r\n    \"process\",\r\n    \"processing\",\r\n    \"produce\",\r\n    \"product\",\r\n    \"production\",\r\n    \"professor\",\r\n    \"profit\",\r\n    \"promotion\",\r\n    \"propane\",\r\n    \"property\",\r\n    \"prose\",\r\n    \"prosecution\",\r\n    \"protest\",\r\n    \"protocol\",\r\n    \"pruner\",\r\n    \"psychiatrist\",\r\n    \"psychology\",\r\n    \"ptarmigan\",\r\n    \"puffin\",\r\n    \"pull\",\r\n    \"puma\",\r\n    \"pump\",\r\n    \"pumpkin\",\r\n    \"punch\",\r\n    \"punishment\",\r\n    \"puppy\",\r\n    \"purchase\",\r\n    \"purple\",\r\n    \"purpose\",\r\n    \"push\",\r\n    \"pvc\",\r\n    \"pyjama\",\r\n    \"pyramid\",\r\n    \"quail\",\r\n    \"quality\",\r\n    \"quart\",\r\n    \"quarter\",\r\n    \"quartz\",\r\n    \"queen\",\r\n    \"question\",\r\n    \"quicksand\",\r\n    \"quiet\",\r\n    \"quill\",\r\n    \"quilt\",\r\n    \"quince\",\r\n    \"quit\",\r\n    \"quiver\",\r\n    \"quotation\",\r\n    \"rabbi\",\r\n    \"rabbit\",\r\n    \"racing\",\r\n    \"radar\",\r\n    \"radiator\",\r\n    \"radio\",\r\n    \"radish\",\r\n    \"raft\",\r\n    \"rail\",\r\n    \"railway\",\r\n    \"rain\",\r\n    \"rainbow\",\r\n    \"raincoat\",\r\n    \"rainstorm\",\r\n    \"rake\",\r\n    \"ramie\",\r\n    \"random\",\r\n    \"range\",\r\n    \"rat\",\r\n    \"rate\",\r\n    \"raven\",\r\n    \"ravioli\",\r\n    \"ray\",\r\n    \"rayon\",\r\n    \"reaction\",\r\n    \"reading\",\r\n    \"reason\",\r\n    \"receipt\",\r\n    \"recess\",\r\n    \"record\",\r\n    \"recorder\",\r\n    \"rectangle\",\r\n    \"red\",\r\n    \"reduction\",\r\n    \"refrigerator\",\r\n    \"refund\",\r\n    \"regret\",\r\n    \"reindeer\",\r\n    \"relation\",\r\n    \"relative\",\r\n    \"religion\",\r\n    \"relish\",\r\n    \"reminder\",\r\n    \"repair\",\r\n    \"replace\",\r\n    \"report\",\r\n    \"representative\",\r\n    \"request\",\r\n    \"resolution\",\r\n    \"respect\",\r\n    \"responsibility\",\r\n    \"rest\",\r\n    \"restaurant\",\r\n    \"result\",\r\n    \"retailer\",\r\n    \"revolve\",\r\n    \"revolver\",\r\n    \"reward\",\r\n    \"rhinoceros\",\r\n    \"rhythm\",\r\n    \"rice\",\r\n    \"richard\",\r\n    \"riddle\",\r\n    \"rifle\",\r\n    \"ring\",\r\n    \"rise\",\r\n    \"risk\",\r\n    \"river\",\r\n    \"riverbed\",\r\n    \"road\",\r\n    \"roadway\",\r\n    \"roast\",\r\n    \"robert\",\r\n    \"robin\",\r\n    \"rock\",\r\n    \"rocket\",\r\n    \"rod\",\r\n    \"roll\",\r\n    \"romania\",\r\n    \"romanian\",\r\n    \"ronald\",\r\n    \"roof\",\r\n    \"room\",\r\n    \"rooster\",\r\n    \"root\",\r\n    \"rose\",\r\n    \"rotate\",\r\n    \"route\",\r\n    \"router\",\r\n    \"rowboat\",\r\n    \"rub\",\r\n    \"rubber\",\r\n    \"rugby\",\r\n    \"rule\",\r\n    \"run\",\r\n    \"russia\",\r\n    \"russian\",\r\n    \"rutabaga\",\r\n    \"ruth\",\r\n    \"sack\",\r\n    \"sagittarius\",\r\n    \"sail\",\r\n    \"sailboat\",\r\n    \"sailor\",\r\n    \"salad\",\r\n    \"salary\",\r\n    \"sale\",\r\n    \"salesman\",\r\n    \"salmon\",\r\n    \"salt\",\r\n    \"sampan\",\r\n    \"samurai\",\r\n    \"sand\",\r\n    \"sandra\",\r\n    \"sandwich\",\r\n    \"santa\",\r\n    \"sarah\",\r\n    \"sardine\",\r\n    \"satin\",\r\n    \"saturday\",\r\n    \"sauce\",\r\n    \"saudi\",\r\n    \"arabia\",\r\n    \"sausage\",\r\n    \"save\",\r\n    \"saw\",\r\n    \"saxophone\",\r\n    \"scale\",\r\n    \"scallion\",\r\n    \"scanner\",\r\n    \"scarecrow\",\r\n    \"scarf\",\r\n    \"scene\",\r\n    \"scent\",\r\n    \"schedule\",\r\n    \"school\",\r\n    \"science\",\r\n    \"scissors\",\r\n    \"scooter\",\r\n    \"scorpio\",\r\n    \"scorpion\",\r\n    \"scraper\",\r\n    \"screen\",\r\n    \"screw\",\r\n    \"screwdriver\",\r\n    \"sea\",\r\n    \"seagull\",\r\n    \"seal\",\r\n    \"seaplane\",\r\n    \"search\",\r\n    \"seashore\",\r\n    \"season\",\r\n    \"seat\",\r\n    \"second\",\r\n    \"secretary\",\r\n    \"secure\",\r\n    \"security\",\r\n    \"seed\",\r\n    \"seeder\",\r\n    \"segment\",\r\n    \"select\",\r\n    \"selection\",\r\n    \"self\",\r\n    \"semicircle\",\r\n    \"semicolon\",\r\n    \"sense\",\r\n    \"sentence\",\r\n    \"separated\",\r\n    \"september\",\r\n    \"servant\",\r\n    \"server\",\r\n    \"session\",\r\n    \"sex\",\r\n    \"shade\",\r\n    \"shadow\",\r\n    \"shake\",\r\n    \"shallot\",\r\n    \"shame\",\r\n    \"shampoo\",\r\n    \"shape\",\r\n    \"share\",\r\n    \"shark\",\r\n    \"sharon\",\r\n    \"shears\",\r\n    \"sheep\",\r\n    \"sheet\",\r\n    \"shelf\",\r\n    \"shell\",\r\n    \"shield\",\r\n    \"shingle\",\r\n    \"ship\",\r\n    \"shirt\",\r\n    \"shock\",\r\n    \"shoe\",\r\n    \"shoemaker\",\r\n    \"shop\",\r\n    \"shorts\",\r\n    \"shoulder\",\r\n    \"shovel\",\r\n    \"show\",\r\n    \"shrimp\",\r\n    \"shrine\",\r\n    \"siamese\",\r\n    \"siberian\",\r\n    \"side\",\r\n    \"sideboard\",\r\n    \"sidecar\",\r\n    \"sidewalk\",\r\n    \"sign\",\r\n    \"signature\",\r\n    \"silica\",\r\n    \"silk\",\r\n    \"sing\",\r\n    \"singer\",\r\n    \"single\",\r\n    \"sink\",\r\n    \"sister\",\r\n    \"sister-in-law\",\r\n    \"size\",\r\n    \"skate\",\r\n    \"skiing\",\r\n    \"skill\",\r\n    \"skin\",\r\n    \"skirt\",\r\n    \"sky\",\r\n    \"slash\",\r\n    \"slave\",\r\n    \"sled\",\r\n    \"sleep\",\r\n    \"sleet\",\r\n    \"slice\",\r\n    \"slime\",\r\n    \"slip\",\r\n    \"slipper\",\r\n    \"slope\",\r\n    \"smash\",\r\n    \"smell\",\r\n    \"smile\",\r\n    \"smoke\",\r\n    \"snail\",\r\n    \"snake\",\r\n    \"sneeze\",\r\n    \"snow\",\r\n    \"snowboarding\",\r\n    \"snowflake\",\r\n    \"snowman\",\r\n    \"snowplow\",\r\n    \"snowstorm\",\r\n    \"soap\",\r\n    \"soccer\",\r\n    \"society\",\r\n    \"sociology\",\r\n    \"sock\",\r\n    \"soda\",\r\n    \"sofa\",\r\n    \"softball\",\r\n    \"softdrink\",\r\n    \"software\",\r\n    \"soil\",\r\n    \"soldier\",\r\n    \"son\",\r\n    \"song\",\r\n    \"soprano\",\r\n    \"sort\",\r\n    \"sound\",\r\n    \"soup\",\r\n    \"sousaphone\",\r\n    \"south\",\r\n    \"africa\",\r\n    \"south\",\r\n    \"america\",\r\n    \"south\",\r\n    \"korea\",\r\n    \"soy\",\r\n    \"soybean\",\r\n    \"space\",\r\n    \"spade\",\r\n    \"spaghetti\",\r\n    \"spain\",\r\n    \"spandex\",\r\n    \"spark\",\r\n    \"sparrow\",\r\n    \"spear\",\r\n    \"specialist\",\r\n    \"speedboat\",\r\n    \"sphere\",\r\n    \"sphynx\",\r\n    \"spider\",\r\n    \"spike\",\r\n    \"spinach\",\r\n    \"spleen\",\r\n    \"sponge\",\r\n    \"spoon\",\r\n    \"spot\",\r\n    \"spring\",\r\n    \"sprout\",\r\n    \"spruce\",\r\n    \"spy\",\r\n    \"square\",\r\n    \"squash\",\r\n    \"squid\",\r\n    \"squirrel\",\r\n    \"stage\",\r\n    \"staircase\",\r\n    \"stamp\",\r\n    \"star\",\r\n    \"start\",\r\n    \"starter\",\r\n    \"state\",\r\n    \"statement\",\r\n    \"station\",\r\n    \"statistic\",\r\n    \"steam\",\r\n    \"steel\",\r\n    \"stem\",\r\n    \"step\",\r\n    \"step-aunt\",\r\n    \"step-brother\",\r\n    \"stepdaughter\",\r\n    \"step-daughter\",\r\n    \"step-father\",\r\n    \"step-grandfather\",\r\n    \"step-grandmother\",\r\n    \"stepmother\",\r\n    \"step-mother\",\r\n    \"step-sister\",\r\n    \"stepson\",\r\n    \"step-son\",\r\n    \"step-uncle\",\r\n    \"steven\",\r\n    \"stew\",\r\n    \"stick\",\r\n    \"stinger\",\r\n    \"stitch\",\r\n    \"stock\",\r\n    \"stocking\",\r\n    \"stomach\",\r\n    \"stone\",\r\n    \"stool\",\r\n    \"stop\",\r\n    \"stopsign\",\r\n    \"stopwatch\",\r\n    \"store\",\r\n    \"storm\",\r\n    \"story\",\r\n    \"stove\",\r\n    \"stranger\",\r\n    \"straw\",\r\n    \"stream\",\r\n    \"street\",\r\n    \"streetcar\",\r\n    \"stretch\",\r\n    \"string\",\r\n    \"structure\",\r\n    \"study\",\r\n    \"sturgeon\",\r\n    \"submarine\",\r\n    \"substance\",\r\n    \"subway\",\r\n    \"success\",\r\n    \"sudan\",\r\n    \"suede\",\r\n    \"sugar\",\r\n    \"suggestion\",\r\n    \"suit\",\r\n    \"summer\",\r\n    \"sun\",\r\n    \"sunday\",\r\n    \"sundial\",\r\n    \"sunflower\",\r\n    \"sunshine\",\r\n    \"supermarket\",\r\n    \"supply\",\r\n    \"support\",\r\n    \"surfboard\",\r\n    \"surgeon\",\r\n    \"surname\",\r\n    \"surprise\",\r\n    \"susan\",\r\n    \"sushi\",\r\n    \"swallow\",\r\n    \"swamp\",\r\n    \"swan\",\r\n    \"sweater\",\r\n    \"sweatshirt\",\r\n    \"sweatshop\",\r\n    \"swedish\",\r\n    \"sweets\",\r\n    \"swim\",\r\n    \"swimming\",\r\n    \"swing\",\r\n    \"swiss\",\r\n    \"switch\",\r\n    \"sword\",\r\n    \"swordfish\",\r\n    \"sycamore\",\r\n    \"syria\",\r\n    \"syrup\",\r\n    \"system\",\r\n    \"table\",\r\n    \"tablecloth\",\r\n    \"tabletop\",\r\n    \"tachometer\",\r\n    \"tadpole\",\r\n    \"tail\",\r\n    \"tailor\",\r\n    \"taiwan\",\r\n    \"talk\",\r\n    \"tank\",\r\n    \"tanker\",\r\n    \"tanzania\",\r\n    \"target\",\r\n    \"taste\",\r\n    \"taurus\",\r\n    \"tax\",\r\n    \"taxi\",\r\n    \"taxicab\",\r\n    \"tea\",\r\n    \"teacher\",\r\n    \"teaching\",\r\n    \"team\",\r\n    \"technician\",\r\n    \"teeth\",\r\n    \"television\",\r\n    \"teller\",\r\n    \"temper\",\r\n    \"temperature\",\r\n    \"temple\",\r\n    \"tempo\",\r\n    \"tendency\",\r\n    \"tennis\",\r\n    \"tenor\",\r\n    \"tent\",\r\n    \"territory\",\r\n    \"test\",\r\n    \"text\",\r\n    \"textbook\",\r\n    \"texture\",\r\n    \"thailand\",\r\n    \"theater\",\r\n    \"theory\",\r\n    \"thermometer\",\r\n    \"thing\",\r\n    \"thistle\",\r\n    \"thomas\",\r\n    \"thought\",\r\n    \"thread\",\r\n    \"thrill\",\r\n    \"throat\",\r\n    \"throne\",\r\n    \"thumb\",\r\n    \"thunder\",\r\n    \"thunderstorm\",\r\n    \"thursday\",\r\n    \"ticket\",\r\n    \"tie\",\r\n    \"tiger\",\r\n    \"tights\",\r\n    \"tile\",\r\n    \"timbale\",\r\n    \"time\",\r\n    \"timer\",\r\n    \"timpani\",\r\n    \"tip\",\r\n    \"tire\",\r\n    \"title\",\r\n    \"toad\",\r\n    \"toast\",\r\n    \"toe\",\r\n    \"toenail\",\r\n    \"toilet\",\r\n    \"tomato\",\r\n    \"tom-tom\",\r\n    \"ton\",\r\n    \"tongue\",\r\n    \"tooth\",\r\n    \"toothbrush\",\r\n    \"toothpaste\",\r\n    \"top\",\r\n    \"tornado\",\r\n    \"tortellini\",\r\n    \"tortoise\",\r\n    \"touch\",\r\n    \"tower\",\r\n    \"town\",\r\n    \"toy\",\r\n    \"tractor\",\r\n    \"trade\",\r\n    \"traffic\",\r\n    \"trail\",\r\n    \"train\",\r\n    \"tramp\",\r\n    \"transaction\",\r\n    \"transmission\",\r\n    \"transport\",\r\n    \"trapezoid\",\r\n    \"tray\",\r\n    \"treatment\",\r\n    \"tree\",\r\n    \"trial\",\r\n    \"triangle\",\r\n    \"trick\",\r\n    \"trigonometry\",\r\n    \"trip\",\r\n    \"trombone\",\r\n    \"trouble\",\r\n    \"trousers\",\r\n    \"trout\",\r\n    \"trowel\",\r\n    \"truck\",\r\n    \"trumpet\",\r\n    \"trunk\",\r\n    \"t-shirt\",\r\n    \"tsunami\",\r\n    \"tub\",\r\n    \"tuba\",\r\n    \"tuesday\",\r\n    \"tugboat\",\r\n    \"tulip\",\r\n    \"tuna\",\r\n    \"tune\",\r\n    \"turkey\",\r\n    \"turkey\",\r\n    \"turkish\",\r\n    \"turn\",\r\n    \"turnip\",\r\n    \"turnover\",\r\n    \"turret\",\r\n    \"turtle\",\r\n    \"tv\",\r\n    \"twig\",\r\n    \"twilight\",\r\n    \"twine\",\r\n    \"twist\",\r\n    \"typhoon\",\r\n    \"tyvek\",\r\n    \"uganda\",\r\n    \"ukraine\",\r\n    \"ukrainian\",\r\n    \"umbrella\",\r\n    \"uncle\",\r\n    \"underclothes\",\r\n    \"underpants\",\r\n    \"undershirt\",\r\n    \"underwear\",\r\n    \"unit\",\r\n    \"united\",\r\n    \"kingdom\",\r\n    \"unshielded\",\r\n    \"use\",\r\n    \"utensil\",\r\n    \"uzbekistan\",\r\n    \"vacation\",\r\n    \"vacuum\",\r\n    \"valley\",\r\n    \"value\",\r\n    \"van\",\r\n    \"vase\",\r\n    \"vault\",\r\n    \"vegetable\",\r\n    \"vegetarian\",\r\n    \"veil\",\r\n    \"vein\",\r\n    \"velvet\",\r\n    \"venezuela\",\r\n    \"venezuelan\",\r\n    \"verdict\",\r\n    \"vermicelli\",\r\n    \"verse\",\r\n    \"vessel\",\r\n    \"vest\",\r\n    \"veterinarian\",\r\n    \"vibraphone\",\r\n    \"vietnam\",\r\n    \"view\",\r\n    \"vinyl\",\r\n    \"viola\",\r\n    \"violet\",\r\n    \"violin\",\r\n    \"virgo\",\r\n    \"viscose\",\r\n    \"vise\",\r\n    \"vision\",\r\n    \"visitor\",\r\n    \"voice\",\r\n    \"volcano\",\r\n    \"volleyball\",\r\n    \"voyage\",\r\n    \"vulture\",\r\n    \"waiter\",\r\n    \"waitress\",\r\n    \"walk\",\r\n    \"wall\",\r\n    \"wallaby\",\r\n    \"wallet\",\r\n    \"walrus\",\r\n    \"war\",\r\n    \"warm\",\r\n    \"wash\",\r\n    \"washer\",\r\n    \"wasp\",\r\n    \"waste\",\r\n    \"watch\",\r\n    \"watchmaker\",\r\n    \"water\",\r\n    \"waterfall\",\r\n    \"wave\",\r\n    \"wax\",\r\n    \"way\",\r\n    \"wealth\",\r\n    \"weapon\",\r\n    \"weasel\",\r\n    \"weather\",\r\n    \"wedge\",\r\n    \"wednesday\",\r\n    \"weed\",\r\n    \"weeder\",\r\n    \"week\",\r\n    \"weight\",\r\n    \"whale\",\r\n    \"wheel\",\r\n    \"whip\",\r\n    \"whiskey\",\r\n    \"whistle\",\r\n    \"white\",\r\n    \"wholesaler\",\r\n    \"whorl\",\r\n    \"wilderness\",\r\n    \"william\",\r\n    \"willow\",\r\n    \"wind\",\r\n    \"windchime\",\r\n    \"window\",\r\n    \"windscreen\",\r\n    \"windshield\",\r\n    \"wine\",\r\n    \"wing\",\r\n    \"winter\",\r\n    \"wire\",\r\n    \"wish\",\r\n    \"witch\",\r\n    \"withdrawal\",\r\n    \"witness\",\r\n    \"wolf\",\r\n    \"woman\",\r\n    \"women\",\r\n    \"wood\",\r\n    \"wool\",\r\n    \"woolen\",\r\n    \"word\",\r\n    \"work\",\r\n    \"workshop\",\r\n    \"worm\",\r\n    \"wound\",\r\n    \"wrecker\",\r\n    \"wren\",\r\n    \"wrench\",\r\n    \"wrinkle\",\r\n    \"wrist\",\r\n    \"writer\",\r\n    \"xylophone\",\r\n    \"yacht\",\r\n    \"yak\",\r\n    \"yam\",\r\n    \"yard\",\r\n    \"yarn\",\r\n    \"year\",\r\n    \"yellow\",\r\n    \"yew\",\r\n    \"yogurt\",\r\n    \"yoke\",\r\n    \"yugoslavian\",\r\n    \"zebra\",\r\n    \"zephyr\",\r\n    \"zipper\",\r\n    \"zone\",\r\n    \"zoo\",\r\n    \"zoology\"\r\n]"
  },
  {
    "path": "LICENSE",
    "content": "Attribution-NonCommercial-ShareAlike 4.0 International\n\n=======================================================================\n\nCreative Commons Corporation (\"Creative Commons\") is not a law firm and\ndoes not provide legal services or legal advice. Distribution of\nCreative Commons public licenses does not create a lawyer-client or\nother relationship. Creative Commons makes its licenses and related\ninformation available on an \"as-is\" basis. Creative Commons gives no\nwarranties regarding its licenses, any material licensed under their\nterms and conditions, or any related information. Creative Commons\ndisclaims all liability for damages resulting from their use to the\nfullest extent possible.\n\nUsing Creative Commons Public Licenses\n\nCreative Commons public licenses provide a standard set of terms and\nconditions that creators and other rights holders may use to share\noriginal works of authorship and other material subject to copyright\nand certain other rights specified in the public license below. The\nfollowing considerations are for informational purposes only, are not\nexhaustive, and do not form part of our licenses.\n\n     Considerations for licensors: Our public licenses are\n     intended for use by those authorized to give the public\n     permission to use material in ways otherwise restricted by\n     copyright and certain other rights. Our licenses are\n     irrevocable. Licensors should read and understand the terms\n     and conditions of the license they choose before applying it.\n     Licensors should also secure all rights necessary before\n     applying our licenses so that the public can reuse the\n     material as expected. Licensors should clearly mark any\n     material not subject to the license. This includes other CC-\n     licensed material, or material used under an exception or\n     limitation to copyright. More considerations for licensors:\n    wiki.creativecommons.org/Considerations_for_licensors\n\n     Considerations for the public: By using one of our public\n     licenses, a licensor grants the public permission to use the\n     licensed material under specified terms and conditions. If\n     the licensor's permission is not necessary for any reason--for\n     example, because of any applicable exception or limitation to\n     copyright--then that use is not regulated by the license. Our\n     licenses grant only permissions under copyright and certain\n     other rights that a licensor has authority to grant. Use of\n     the licensed material may still be restricted for other\n     reasons, including because others have copyright or other\n     rights in the material. A licensor may make special requests,\n     such as asking that all changes be marked or described.\n     Although not required by our licenses, you are encouraged to\n     respect those requests where reasonable. More considerations\n     for the public:\n    wiki.creativecommons.org/Considerations_for_licensees\n\n=======================================================================\n\nCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International\nPublic License\n\nBy exercising the Licensed Rights (defined below), You accept and agree\nto be bound by the terms and conditions of this Creative Commons\nAttribution-NonCommercial-ShareAlike 4.0 International Public License\n(\"Public License\"). To the extent this Public License may be\ninterpreted as a contract, You are granted the Licensed Rights in\nconsideration of Your acceptance of these terms and conditions, and the\nLicensor grants You such rights in consideration of benefits the\nLicensor receives from making the Licensed Material available under\nthese terms and conditions.\n\n\nSection 1 -- Definitions.\n\n  a. Adapted Material means material subject to Copyright and Similar\n     Rights that is derived from or based upon the Licensed Material\n     and in which the Licensed Material is translated, altered,\n     arranged, transformed, or otherwise modified in a manner requiring\n     permission under the Copyright and Similar Rights held by the\n     Licensor. For purposes of this Public License, where the Licensed\n     Material is a musical work, performance, or sound recording,\n     Adapted Material is always produced where the Licensed Material is\n     synched in timed relation with a moving image.\n\n  b. Adapter's License means the license You apply to Your Copyright\n     and Similar Rights in Your contributions to Adapted Material in\n     accordance with the terms and conditions of this Public License.\n\n  c. BY-NC-SA Compatible License means a license listed at\n     creativecommons.org/compatiblelicenses, approved by Creative\n     Commons as essentially the equivalent of this Public License.\n\n  d. Copyright and Similar Rights means copyright and/or similar rights\n     closely related to copyright including, without limitation,\n     performance, broadcast, sound recording, and Sui Generis Database\n     Rights, without regard to how the rights are labeled or\n     categorized. For purposes of this Public License, the rights\n     specified in Section 2(b)(1)-(2) are not Copyright and Similar\n     Rights.\n\n  e. Effective Technological Measures means those measures that, in the\n     absence of proper authority, may not be circumvented under laws\n     fulfilling obligations under Article 11 of the WIPO Copyright\n     Treaty adopted on December 20, 1996, and/or similar international\n     agreements.\n\n  f. Exceptions and Limitations means fair use, fair dealing, and/or\n     any other exception or limitation to Copyright and Similar Rights\n     that applies to Your use of the Licensed Material.\n\n  g. License Elements means the license attributes listed in the name\n     of a Creative Commons Public License. The License Elements of this\n     Public License are Attribution, NonCommercial, and ShareAlike.\n\n  h. Licensed Material means the artistic or literary work, database,\n     or other material to which the Licensor applied this Public\n     License.\n\n  i. Licensed Rights means the rights granted to You subject to the\n     terms and conditions of this Public License, which are limited to\n     all Copyright and Similar Rights that apply to Your use of the\n     Licensed Material and that the Licensor has authority to license.\n\n  j. Licensor means the individual(s) or entity(ies) granting rights\n     under this Public License.\n\n  k. NonCommercial means not primarily intended for or directed towards\n     commercial advantage or monetary compensation. For purposes of\n     this Public License, the exchange of the Licensed Material for\n     other material subject to Copyright and Similar Rights by digital\n     file-sharing or similar means is NonCommercial provided there is\n     no payment of monetary compensation in connection with the\n     exchange.\n\n  l. Share means to provide material to the public by any means or\n     process that requires permission under the Licensed Rights, such\n     as reproduction, public display, public performance, distribution,\n     dissemination, communication, or importation, and to make material\n     available to the public including in ways that members of the\n     public may access the material from a place and at a time\n     individually chosen by them.\n\n  m. Sui Generis Database Rights means rights other than copyright\n     resulting from Directive 96/9/EC of the European Parliament and of\n     the Council of 11 March 1996 on the legal protection of databases,\n     as amended and/or succeeded, as well as other essentially\n     equivalent rights anywhere in the world.\n\n  n. You means the individual or entity exercising the Licensed Rights\n     under this Public License. Your has a corresponding meaning.\n\n\nSection 2 -- Scope.\n\n  a. License grant.\n\n       1. Subject to the terms and conditions of this Public License,\n          the Licensor hereby grants You a worldwide, royalty-free,\n          non-sublicensable, non-exclusive, irrevocable license to\n          exercise the Licensed Rights in the Licensed Material to:\n\n            a. reproduce and Share the Licensed Material, in whole or\n               in part, for NonCommercial purposes only; and\n\n            b. produce, reproduce, and Share Adapted Material for\n               NonCommercial purposes only.\n\n       2. Exceptions and Limitations. For the avoidance of doubt, where\n          Exceptions and Limitations apply to Your use, this Public\n          License does not apply, and You do not need to comply with\n          its terms and conditions.\n\n       3. Term. The term of this Public License is specified in Section\n          6(a).\n\n       4. Media and formats; technical modifications allowed. The\n          Licensor authorizes You to exercise the Licensed Rights in\n          all media and formats whether now known or hereafter created,\n          and to make technical modifications necessary to do so. The\n          Licensor waives and/or agrees not to assert any right or\n          authority to forbid You from making technical modifications\n          necessary to exercise the Licensed Rights, including\n          technical modifications necessary to circumvent Effective\n          Technological Measures. For purposes of this Public License,\n          simply making modifications authorized by this Section 2(a)\n          (4) never produces Adapted Material.\n\n       5. Downstream recipients.\n\n            a. Offer from the Licensor -- Licensed Material. Every\n               recipient of the Licensed Material automatically\n               receives an offer from the Licensor to exercise the\n               Licensed Rights under the terms and conditions of this\n               Public License.\n\n            b. Additional offer from the Licensor -- Adapted Material.\n               Every recipient of Adapted Material from You\n               automatically receives an offer from the Licensor to\n               exercise the Licensed Rights in the Adapted Material\n               under the conditions of the Adapter's License You apply.\n\n            c. No downstream restrictions. You may not offer or impose\n               any additional or different terms or conditions on, or\n               apply any Effective Technological Measures to, the\n               Licensed Material if doing so restricts exercise of the\n               Licensed Rights by any recipient of the Licensed\n               Material.\n\n       6. No endorsement. Nothing in this Public License constitutes or\n          may be construed as permission to assert or imply that You\n          are, or that Your use of the Licensed Material is, connected\n          with, or sponsored, endorsed, or granted official status by,\n          the Licensor or others designated to receive attribution as\n          provided in Section 3(a)(1)(A)(i).\n\n  b. Other rights.\n\n       1. Moral rights, such as the right of integrity, are not\n          licensed under this Public License, nor are publicity,\n          privacy, and/or other similar personality rights; however, to\n          the extent possible, the Licensor waives and/or agrees not to\n          assert any such rights held by the Licensor to the limited\n          extent necessary to allow You to exercise the Licensed\n          Rights, but not otherwise.\n\n       2. Patent and trademark rights are not licensed under this\n          Public License.\n\n       3. To the extent possible, the Licensor waives any right to\n          collect royalties from You for the exercise of the Licensed\n          Rights, whether directly or through a collecting society\n          under any voluntary or waivable statutory or compulsory\n          licensing scheme. In all other cases the Licensor expressly\n          reserves any right to collect such royalties, including when\n          the Licensed Material is used other than for NonCommercial\n          purposes.\n\n\nSection 3 -- License Conditions.\n\nYour exercise of the Licensed Rights is expressly made subject to the\nfollowing conditions.\n\n  a. Attribution.\n\n       1. If You Share the Licensed Material (including in modified\n          form), You must:\n\n            a. retain the following if it is supplied by the Licensor\n               with the Licensed Material:\n\n                 i. identification of the creator(s) of the Licensed\n                    Material and any others designated to receive\n                    attribution, in any reasonable manner requested by\n                    the Licensor (including by pseudonym if\n                    designated);\n\n                ii. a copyright notice;\n\n               iii. a notice that refers to this Public License;\n\n                iv. a notice that refers to the disclaimer of\n                    warranties;\n\n                 v. a URI or hyperlink to the Licensed Material to the\n                    extent reasonably practicable;\n\n            b. indicate if You modified the Licensed Material and\n               retain an indication of any previous modifications; and\n\n            c. indicate the Licensed Material is licensed under this\n               Public License, and include the text of, or the URI or\n               hyperlink to, this Public License.\n\n       2. You may satisfy the conditions in Section 3(a)(1) in any\n          reasonable manner based on the medium, means, and context in\n          which You Share the Licensed Material. For example, it may be\n          reasonable to satisfy the conditions by providing a URI or\n          hyperlink to a resource that includes the required\n          information.\n       3. If requested by the Licensor, You must remove any of the\n          information required by Section 3(a)(1)(A) to the extent\n          reasonably practicable.\n\n  b. ShareAlike.\n\n     In addition to the conditions in Section 3(a), if You Share\n     Adapted Material You produce, the following conditions also apply.\n\n       1. The Adapter's License You apply must be a Creative Commons\n          license with the same License Elements, this version or\n          later, or a BY-NC-SA Compatible License.\n\n       2. You must include the text of, or the URI or hyperlink to, the\n          Adapter's License You apply. You may satisfy this condition\n          in any reasonable manner based on the medium, means, and\n          context in which You Share Adapted Material.\n\n       3. You may not offer or impose any additional or different terms\n          or conditions on, or apply any Effective Technological\n          Measures to, Adapted Material that restrict exercise of the\n          rights granted under the Adapter's License You apply.\n\n\nSection 4 -- Sui Generis Database Rights.\n\nWhere the Licensed Rights include Sui Generis Database Rights that\napply to Your use of the Licensed Material:\n\n  a. for the avoidance of doubt, Section 2(a)(1) grants You the right\n     to extract, reuse, reproduce, and Share all or a substantial\n     portion of the contents of the database for NonCommercial purposes\n     only;\n\n  b. if You include all or a substantial portion of the database\n     contents in a database in which You have Sui Generis Database\n     Rights, then the database in which You have Sui Generis Database\n     Rights (but not its individual contents) is Adapted Material,\n     including for purposes of Section 3(b); and\n\n  c. You must comply with the conditions in Section 3(a) if You Share\n     all or a substantial portion of the contents of the database.\n\nFor the avoidance of doubt, this Section 4 supplements and does not\nreplace Your obligations under this Public License where the Licensed\nRights include other Copyright and Similar Rights.\n\n\nSection 5 -- Disclaimer of Warranties and Limitation of Liability.\n\n  a. UNLESS OTHERWISE SEPARATELY UNDERTAKEN BY THE LICENSOR, TO THE\n     EXTENT POSSIBLE, THE LICENSOR OFFERS THE LICENSED MATERIAL AS-IS\n     AND AS-AVAILABLE, AND MAKES NO REPRESENTATIONS OR WARRANTIES OF\n     ANY KIND CONCERNING THE LICENSED MATERIAL, WHETHER EXPRESS,\n     IMPLIED, STATUTORY, OR OTHER. THIS INCLUDES, WITHOUT LIMITATION,\n     WARRANTIES OF TITLE, MERCHANTABILITY, FITNESS FOR A PARTICULAR\n     PURPOSE, NON-INFRINGEMENT, ABSENCE OF LATENT OR OTHER DEFECTS,\n     ACCURACY, OR THE PRESENCE OR ABSENCE OF ERRORS, WHETHER OR NOT\n     KNOWN OR DISCOVERABLE. WHERE DISCLAIMERS OF WARRANTIES ARE NOT\n     ALLOWED IN FULL OR IN PART, THIS DISCLAIMER MAY NOT APPLY TO YOU.\n\n  b. TO THE EXTENT POSSIBLE, IN NO EVENT WILL THE LICENSOR BE LIABLE\n     TO YOU ON ANY LEGAL THEORY (INCLUDING, WITHOUT LIMITATION,\n     NEGLIGENCE) OR OTHERWISE FOR ANY DIRECT, SPECIAL, INDIRECT,\n     INCIDENTAL, CONSEQUENTIAL, PUNITIVE, EXEMPLARY, OR OTHER LOSSES,\n     COSTS, EXPENSES, OR DAMAGES ARISING OUT OF THIS PUBLIC LICENSE OR\n     USE OF THE LICENSED MATERIAL, EVEN IF THE LICENSOR HAS BEEN\n     ADVISED OF THE POSSIBILITY OF SUCH LOSSES, COSTS, EXPENSES, OR\n     DAMAGES. WHERE A LIMITATION OF LIABILITY IS NOT ALLOWED IN FULL OR\n     IN PART, THIS LIMITATION MAY NOT APPLY TO YOU.\n\n  c. The disclaimer of warranties and limitation of liability provided\n     above shall be interpreted in a manner that, to the extent\n     possible, most closely approximates an absolute disclaimer and\n     waiver of all liability.\n\n\nSection 6 -- Term and Termination.\n\n  a. This Public License applies for the term of the Copyright and\n     Similar Rights licensed here. However, if You fail to comply with\n     this Public License, then Your rights under this Public License\n     terminate automatically.\n\n  b. Where Your right to use the Licensed Material has terminated under\n     Section 6(a), it reinstates:\n\n       1. automatically as of the date the violation is cured, provided\n          it is cured within 30 days of Your discovery of the\n          violation; or\n\n       2. upon express reinstatement by the Licensor.\n\n     For the avoidance of doubt, this Section 6(b) does not affect any\n     right the Licensor may have to seek remedies for Your violations\n     of this Public License.\n\n  c. For the avoidance of doubt, the Licensor may also offer the\n     Licensed Material under separate terms or conditions or stop\n     distributing the Licensed Material at any time; however, doing so\n     will not terminate this Public License.\n\n  d. Sections 1, 5, 6, 7, and 8 survive termination of this Public\n     License.\n\n\nSection 7 -- Other Terms and Conditions.\n\n  a. The Licensor shall not be bound by any additional or different\n     terms or conditions communicated by You unless expressly agreed.\n\n  b. Any arrangements, understandings, or agreements regarding the\n     Licensed Material not stated herein are separate from and\n     independent of the terms and conditions of this Public License.\n\n\nSection 8 -- Interpretation.\n\n  a. For the avoidance of doubt, this Public License does not, and\n     shall not be interpreted to, reduce, limit, restrict, or impose\n     conditions on any use of the Licensed Material that could lawfully\n     be made without permission under this Public License.\n\n  b. To the extent possible, if any provision of this Public License is\n     deemed unenforceable, it shall be automatically reformed to the\n     minimum extent necessary to make it enforceable. If the provision\n     cannot be reformed, it shall be severed from this Public License\n     without affecting the enforceability of the remaining terms and\n     conditions.\n\n  c. No term or condition of this Public License will be waived and no\n     failure to comply consented to unless expressly agreed to by the\n     Licensor.\n\n  d. Nothing in this Public License constitutes or may be interpreted\n     as a limitation upon, or waiver of, any privileges and immunities\n     that apply to the Licensor or You, including from the legal\n     processes of any jurisdiction or authority.\n\n=======================================================================\n\nCreative Commons is not a party to its public\nlicenses. Notwithstanding, Creative Commons may elect to apply one of\nits public licenses to material it publishes and in those instances\nwill be considered the “Licensor.” The text of the Creative Commons\npublic licenses is dedicated to the public domain under the CC0 Public\nDomain Dedication. Except for the limited purpose of indicating that\nmaterial is shared under a Creative Commons public license or as\notherwise permitted by the Creative Commons policies published at\ncreativecommons.org/policies, Creative Commons does not authorize the\nuse of the trademark \"Creative Commons\" or any other trademark or logo\nof Creative Commons without its prior written consent including,\nwithout limitation, in connection with any unauthorized modifications\nto any of its public licenses or any other arrangements,\nunderstandings, or agreements concerning use of licensed material. For\nthe avoidance of doubt, this paragraph does not form part of the\npublic licenses.\n\nCreative Commons may be contacted at creativecommons.org.\n"
  },
  {
    "path": "README.md",
    "content": "# Darwin: A Tailored GPT for the Scientific Domain 🇦🇺\n![logo](assets/logo.png)\n\n**Organization: [University of New South Wales（UNSW) AI4Science](https://www.masterai.com.au) & [GreenDynamics AI](https://www.greendynamics.com.au)**\n\nDarwin is an open-source project dedicated to pretrain and fine-tune the LLaMA model on scientific literature and datasets. Specifically designed for the scientific domain with an emphasis on materials science, chemistry, and physics, Darwin integrates structured and unstructured scientific knowledge to enhance the efficacy of language models in scientific research. \n\n> **Usage and License Notices**: <a rel=\"license\" href=\"http://creativecommons.org/licenses/by-nc-sa/4.0/\"><img alt=\"Creative Commons License\" style=\"border-width:0\" src=\"https://i.creativecommons.org/l/by-nc-sa/4.0/88x31.png\" /></a>\nDarwin is licensed and intended for research use only. The dataset is licensed under CC BY NC 4.0, allowing non-commercial use. Models trained using this dataset should not be used outside of research purposes. The weight diff is also under CC BY NC 4.0 license\n\n## Update\n**[2024.11.20]**\n\n![TOC](assets/TOC.png)\n\n**Key Achievements**\n1. Proved that Darwin’s fine-tuning strategies (QA + multi-task) substantially improve performance on diverse ML tasks.\n2. Established Darwin as a competitive model, bridging the gap between specialized ML methods and large-scale generalist models like GPT-4.\n \n**Model Performance Insights**\n1. Comparison of QA + Multi-task Strategies Across LLaMA Variants\n    - Conducted extensive comparisons of QA and multi-task fine-tuning strategies on LLaMA1, LLaMA2, LLaMA3, and LLaMA3.1 models.\n    - Finding: LLaMA1 with QA + multi-task fine-tuning achieves the best performance, outperforming all other variants.\n2. Evaluation Against Other Models\n\t- Demonstrated that Darwin consistently surpasses most ML methods, GPT-3.5 fine-tuned models, and even GPT-4 in few-shot learning tasks.\n\t- Although some specialized models still maintain state-of-the-art results, Darwin achieves competitive performance across a broad range of tasks.\n3. Comparison of Full Fine-tuning vs. LoRA\n\t- Investigated the use of LoRA fine-tuning and observed significantly lower performance compared to full fine-tuning.\n4. SFT on Non-pretrained Architectures\n\t- Successfully applied supervised fine-tuning (SFT) on non-pretrained LLaMA architectures, proving that models can acquire domain-specific knowledge effectively through fine-tuning alone.\n\n**Data Strategies and Insights**\n1. Impact of QA Data on Model Performance\n\t- Verified that both QA fine-tuning and multi-task learning improve model performance, not only for LLaMA but also for other architectures like Mistral.\n\t- Mixing QA data with general data improves model performance without causing model annealing.\n2. Synchronized Data and Format Matching\n\t- Tested the use of synchronized (sync) data for target tasks.\n\t- Findings:\n\t    - Sync data with similar format improves performance significantly.\n\t    - Sync data with differing formats degrades performance.\n\n**DARWIN 1.5 Model Weights**\nDownload the checkpoints of the Darwin 1.5-7B Weights from [onedrive](https://aigreendynamics-my.sharepoint.com/:f:/g/personal/yuwei_greendynamics_com_au/Evuc5Tl_Jb9LrbZLh1ydcnMBt87Tt69BogUQ35PO362ZUg?e=K08PEy). \n\n**Note**: For support tasks of two versions, please refer to Appendix G in [DARWIN 1.0 paper](https://arxiv.org/pdf/2308.13565) for DARWIN 1.0, and Appendix A in [DARWIN 1.5 paper](https://arxiv.org/pdf/2412.11970?) for DARWIN 1.5. DARWIN 1.5 has more support tasks than 1.0, and for both versions, you are also welcome to try other classification/regression tasks in zero-shot/few-shot ways. But only version 1.0 supports an inverse design task for organic solar cell.\n\n**[2024.02.15]** SOTA in MatBench by Material Projects: DARWIN is the SOTA model in experimental bandgap prediction tasks and metallic classification tasks, better than Fine-tuned GPT3.5 and dedicated ML models. https://matbench.materialsproject.org/Leaderboards%20Per-Task/matbench_v0.1_matbench_expt_gap/ \n\n**☆ [2023.09.15]Google Colab Version available:** Try our DARWIN with Google Colab: **[inference.ipynb](https://github.com/MasterAI-EAM/Darwin/blob/main/inference.ipynb)** \n\n## Model Overview\n\nDarwin, based on the 7B LLaMA model, is trained on over 100,000 instruction-following data points generated by the Darwin Scientific Instruction Generator (SIG) from various scientific FAIR datasets and a literature corpus. By focusing on the factual correctness of the model's responses, Darwin represents a significant stride towards leveraging Large Language Models (LLMs) for scientific discovery. Preliminary human evaluations indicate that Darwin 7B outperforms GPT-4 in scientific Q&A and fine-tuned GPT-3 in solving chemistry problems (like gptChem).\n\nWe are actively developing Darwin for more advanced scientific domain experiments, and we're also integrating Darwin with LangChain to solve more complex scientific tasks (like a private research assistant for personal computers).\n\nPlease note, Darwin is still under development, and many limitations need to be addressed. Most importantly, we have yet to fine-tune Darwin for maximum safety. We encourage users to report any concerning behavior to help improve the model's safety and ethical considerations.\n\n\nhttps://github.com/MasterAI-EAM/Darwin/assets/40589347/d70ee4d6-8177-471c-9b59-2fa4b58c3752\n\n\n[DEMO LINK](https://www.masterai.com.au/darwin)\n\n## Model Comparison\n\n![compare](assets/intro.png)\n\n## Getting Started\n\n### Installation\n\nFirst install the requirements:\n\n```bash\npip install -r requirements.txt\n```\n### Preparing the Darwin Weights\n\nDownload the checkpoints of the Darwin-7B Weights from [onedrive](https://aigreendynamics-my.sharepoint.com/:f:/g/personal/yuwei_greendynamics_com_au/Euu1OzZTOS5OsQvVTRNV_gcBa67ehvk6uN6hJIHnBLOkDg?e=x5wxfk). Once you've downloaded the model, you can try our demo:\n```bash \npython inference.py <your path to darwin-7b>\n```\n\nPlease note, the inference requires at least 10GB of GPU memory for Darwin 7B. \n\n## Fine-tuning\nTo further fine-tune our Darwin-7b with different datasets, below is a command that works on a machine with 4 A100 80G GPUs.\n```bash\ntorchrun  --nproc_per_node=8 --master_port=1212 train.py \\\n    --model_name_or_path <your path to darwin-7b> \\\n    --data_path <your path to dataset> \\\n    --bf16 True \\\n    --output_dir <your output dir> \\\n    --num_train_epochs 3 \\\n    --per_device_train_batch_size 1 \\\n    --per_device_eval_batch_size 1 \\\n    --gradient_accumulation_steps 1 \\\n    --evaluation_strategy \"no\" \\\n    --save_strategy \"steps\" \\\n    --save_steps 500 \\\n    --save_total_limit 1 \\\n    --learning_rate 2e-5 \\\n    --weight_decay 0. \\\n    --warmup_ratio 0.03 \\\n    --lr_scheduler_type \"cosine\" \\\n    --logging_steps 1 \\\n    --fsdp \"full_shard auto_wrap\" \\\n    --fsdp_transformer_layer_cls_to_wrap 'LlamaDecoderLayer' \\\n    --tf32 False\n```\n\n## Datasets Information\n\nOur data comes from two primary sources:\n\nA raw literature corpus containing 6.0M papers on materials science, chemistry, and physics was published after 2000. The publishers include ACS, RSC, Springer Nature, Wiley, and Elsevier. We thank them for their support.\n\nFAIR Datasets - We've collected data from 16 FAIR Datasets.\n\n### Data Generation\nWe developed Darwin-SIG to generate scientific instructions. It can memorize long texts from full literature texts (average ~5000 words) and generate question-and-answer (Q&A) data based on scientific literature keywords (from **[web of science API](https://github.com/Clarivate-SAR/wos-excel-converter))**\n\n> Note: You could also use GPT3.5 or GPT-4 for generation, but these options might be costly.\n\nPlease be aware that we can't share the training dataset due to agreements with the publishers.\n\n## **Authors**\n\nThis project is a collaborative effort by the following:\n\nUNSW & GreenDynamics: [Tong Xie](https://github.com/0xTong), Shaozhou Wang\n\nUNSW: [Imran Razzak](https://imranrazzak.github.io/index.html), Cody Huang\n\nUSYD & DARE Centre: [Clara Grazian](https://github.com/cgrazian)\n\nGreenDynamics: [Yuwei Wan](https://yuweiwan.github.io/),Yixuan Liu\n\n[Bram Hoex](https://unswhoexgroup.com/) and [Wenjie Zhang](https://www.cse.unsw.edu.au/~zhangw/) from UNSW Engineering advised all.\n\n## **Citation**\n\nIf you use the data or code from this repository in your work, please cite it accordingly.\n\nDAWRIN Foundational Large Language Model & Semi-Self Instruct Fine Tuning (DARWIN 1.5)\n```\n@misc{xie2025darwin15largelanguage,\n      title={DARWIN 1.5: Large Language Models as Materials Science Adapted Learners}, \n      author={Tong Xie and Yuwei Wan and Yixuan Liu and Yuchen Zeng and Shaozhou Wang and Wenjie Zhang and Clara Grazian and Chunyu Kit and Wanli Ouyang and Dongzhan Zhou and Bram Hoex},\n      year={2025},\n      eprint={2412.11970},\n      archivePrefix={arXiv},\n      primaryClass={cs.CL},\n      url={https://arxiv.org/abs/2412.11970}, \n}\n```\n\nDAWRIN Foundational Large Language Model & Semi-Self Instruct Fine Tuning (DARWIN 1.0)\n```\n@misc{xie2023darwin,\n      title={DARWIN Series: Domain Specific Large Language Models for Natural Science}, \n      author={Tong Xie and Yuwei Wan and Wei Huang and Zhenyu Yin and Yixuan Liu and Shaozhou Wang and Qingyuan Linghu and Chunyu Kit and Clara Grazian and Wenjie Zhang and Imran Razzak and Bram Hoex},\n      year={2023},\n      eprint={2308.13565},\n      archivePrefix={arXiv},\n      primaryClass={cs.CL}\n}\n```\n\nFine-tuned GPT-3 & LLaMA for Material Discovery (Single Task Training)\n```\n@article{xie2024creation,\n  title={Creation of a structured solar cell material dataset and performance prediction using large language models},\n  author={Xie, Tong and Wan, Yuwei and Zhou, Yufei and Huang, Wei and Liu, Yixuan and Linghu, Qingyuan and Wang, Shaozhou and Kit, Chunyu and Grazian, Clara and Zhang, Wenjie and others},\n  journal={Patterns},\n  volume={5},\n  number={5},\n  year={2024},\n  publisher={Elsevier}\n}\n```\n\n\n## **Acknowledgements**\n\nThis project has referred to the following open-source projects:\n\n- Meta LLaMA: **[LLaMA](https://github.com/facebookresearch/llama)**\n- Stanford Alpaca: **[Alpaca](https://github.com/tatsu-lab/stanford_alpaca)**\n- gptchem: **[gptchem](https://github.com/kjappelbaum/gptchem)**\n\nSpecial thanks to NCI Australia for their HPC support. \n\n**We continuously expand Darwin's development Team. Join us on this exciting journey of advancing scientific research with AI!**\n\nFor PhD or PostDoc positions, please get in touch with tong.xie@unsw.edu.au or b.hoex@unsw.edu.au for details.\n\nFor other positions, please visit www.greendynamics.com.au \n"
  },
  {
    "path": "SII_MDP/README.md",
    "content": "This is the directory for paper \"LARGE LANGUAGE MODELS AS MASTER KEY: UNLOCKING THE SECRETS OF MATERIALS SCIENCE\", which presents a new natural language processing (NLP) task called structured information inference (SII) to address the complexities of information extraction at the device level in material science. This project is part of the whole DARWIN plan. The original data of this project is from https://www.nature.com/articles/s41560-021-00941-3.\n\nThe instructions of code:\n\n- data\n  - regression360.json: train dataset of material & device prediction (MDP) regression task\n  - sii360.json: train dataset of SII task\n  - regression40.json: test dataset of material & device prediction (MDP) regression task\n  - sii40.json: test dataset of SII task\n  - original_text.json: original text of 40 papers in SII test dataset\n- [train](https://github.com/MasterAI-EAM/Darwin/blob/main/train.py): code for training LLaMA-7B (outside in main directory)\n- sii_test.py: code for running test of SII task\n- regression_test.py: code for runing test of MDP regression task.\n- sii_evaluate.ipynb: code for evaluating SII results.\n- regression_evaluate.py: code for evaluating MDP regression results.\n\n\n## Data Format\nsii360.json/regression360.json/sii40.json/regression40.json is JSON file containing a list of dictionaries, and each dictionary contains the following fields:\n- `instruction`: `str`, describes the task the model should perform. For SII, we use \"Summarize stack and method information from given paragraph about solar cell\". For MDP, we use \"What's the PCE of the perovskite solar cell with the parameters below\".\n- `input`: `str`, input for the task. For SII, input is original text of paper. For MDP, input is schema with corresponding values.\n- `output`: `str`, the answer to the instruction. For SII, answer is schema with corresponding values. For MDP, answer is PCE value (and Voc, Jsc, FF)\n\n## Getting Started\n\nFirst install the requirements in the main directory:\n\n```bash\npip install -r requirements.txt\n```\n\nThen download the checkpoints of the open-source LLaMA-7B weights from huggingface. \n\n## Fine-tuning\nTo fine-tune LLaMA-7b with SII/MDP datasets, below is a command that works on a machine with 4 A100 80G GPUs in FSDP `full_shard` mode.\nReplace `<your_random_port>` with a port of your own, `<your_path_to_hf_converted_llama_ckpt_and_tokenizer>` with the\npath to your converted checkpoint and tokenizer, and `<your_output_dir>` with where you want to store your outputs.\n```bash\ntorchrun  --nproc_per_node=8 --master_port=<your_random_port> train.py \\\n    --model_name_or_path <your path to LLaMA-7b> \\\n    --data_path <your path to dataset> \\\n    --bf16 True \\\n    --output_dir <your output dir> \\\n    --num_train_epochs 3 \\\n    --per_device_train_batch_size 1 \\\n    --per_device_eval_batch_size 1 \\\n    --gradient_accumulation_steps 1 \\\n    --evaluation_strategy \"no\" \\\n    --save_strategy \"steps\" \\\n    --save_steps 500 \\\n    --save_total_limit 1 \\\n    --learning_rate 2e-5 \\\n    --weight_decay 0. \\\n    --warmup_ratio 0.03 \\\n    --lr_scheduler_type \"cosine\" \\\n    --logging_steps 1 \\\n    --fsdp \"full_shard auto_wrap\" \\\n    --fsdp_transformer_layer_cls_to_wrap 'LlamaDecoderLayer' \\\n    --tf32 False\n```\n\nTo run on more gpus, you may prefer to turn down `gradient_accumulation_steps` to keep a global batch size of 128. Global batch size has not been tested for optimality.\n\n\n## **Authors**\n\nThis project is a collaborative effort by the following:\n\nUNSW: Tong Xie, Shaozhou Wang, Qingyuan Linghu, Wei Huang, Wenjie Zhang, Bram Hoex\n\nCityU HK: Yuwei Wan, Yufei Zhou, Chunyu Kit\n\nUniversity of Sydney: Clara Grazian\n\nGreenDynamics: Yixuan Liu\n\nAll advised by Bram Hoex from UNSW Engineering\n\n## **Citation**\n\nIf you use the data or code from this repository in your work, please cite it accordingly.\n\n## **Acknowledgements**\n\nThis project has referred to the following open-source projects:\n\n- Meta LLaMA: **[LLaMA](https://github.com/facebookresearch/llama)**\n- Stanford Alpaca: **[Alpaca](https://github.com/tatsu-lab/stanford_alpaca)**\n"
  },
  {
    "path": "SII_MDP/data/README",
    "content": "\n"
  },
  {
    "path": "SII_MDP/data/original_text.json",
    "content": "[\r\n    \"The information of all materials and the preparation of precursor solutions are provided in Supplementary material, also can be found in our previous report . ITO-coated glass with a sheet resistance of 10\\u202f\\u03a9 sq-1 was ultrasonically cleaned by detergent, deionized water in sequence. PEDOT:PSS was spin-coated onto the ITO substrates at 3000\\u202frpm followed by baking at 120\\u202f\\u00b0C for 20\\u202fmin in the air. The same process parameters of spin-coating are suitable for DMSO-doped PEDOT:PSS. The mixed lead precursor solution was preheated at 90\\u202f\\u00b0C on a hot plate and spin-coated at 6000\\u202frpm onto the ITO\\\\/PEDOT:PSS substrates. The ITO\\\\/PEDOT:PSS substrates were preheated and kept at 40\\u202f\\u00b0C during the whole spin-coating process, which was realized by using the spin-coater with the function of substrate-preheating. And then the MAI precursor solution with different 1,6-DD content (0\\u202fwt%, 0.025\\u202fwt%, 0.05\\u202fwt%, 0.075\\u202fwt%, and 0.1\\u202fwt%) was dropping-coated, waiting for 30\\u202fs after the liquid spreading evenly, and spin-coated at 6000\\u202frpm followed annealing at 90\\u202f\\u00b0C for 40\\u202fmin. Then PCBM:BCP blend solution was spin-coated on the perovskite film at 1000\\u202frpm. Finally, Ag metal layer was deposited by thermal evaporation through a shadow mask which determined the cell area of 0.1\\u202fcm2. Except for the perovskite preparation process was performed in an argon-filled glove box, almost all solution processes were performed in the air.\\n\\nX-ray diffraction (XRD, Rigaku D\\\\/MAX 2500) with Cu K\\u03b1 radiation was carried out to record the crystal structure of the perovskite film. Ultraviolet-visible spectroscopy (UV\\u2013vis) of perovskite film was observed with a Jasco-4000 spectrophotometer. The film surface morphology of the final perovskite films were investigated by field-emission scanning electron microscope (SEM, Hitachi SU-8010), atomic force microscopy and conducting atomic force microscopy (AFM and C-AFM, Bruker INNOVA SPM). The film thickness was recorded by KLA-Tencor AlphaStep D-100 Stylus Profiler. Steady-state photoluminescence spectra (PL) and time-resolved photoluminescence of spectra (TRPL) the film were recorded with a Jobin Yvon FluoroLog-3 fluorescence spectrometer to explore the defect passivation and nonradiative recombination. Electrochemical Impedance Spectroscopy (EIS) measurements (Zahner-Zennium equipment) were performed in a frequency range from 1\\u202fHz to 500\\u202fMHz to investigate the interfacial contact and charge transport. X-ray photoelectron spectroscopy (XPS) characterization were conducted by Thermo Scientific ESCALAB250Xi. Contact angle and surface energy measurements were recorded with Drop Shape Analyzer (Kr\\u00fcss DSA25S). The current density-voltage (J-V) characteristics of the devices were measured in an argon-filled glove box, with a programmed Keithley 2400 sourcemeter under illumination of a Newport Oriel 150\\u202fW solar simulator (AM 1.5G, 100\\u202fmW\\u202fcm-2). The light intensity of the solar simulator was calibrated with a solar reference cell (SRC-1000-TC-QZ, VLSI standards, Inc.). All devices were kept in the air without encapsulation.\\n\\n\",\r\n    \"Unless otherwise stated, all chemicals were purchased from Sigma Aldrich and used as received. PCBM (phenyl-C61-butyric acid methyl ester, >99%) and PEDOT:PSS aqueous solution were purchased from Lumtec. PbI2 (99.9985%) was obtained from Alfa Aesar. Formamidinium iodide (FAI, CH(NH2)2I) and methylammonium bromide (MABr, CH3NH3Br) were acquired from Dyesol.\\n\\nPCBM was dissolved in chlorobenzene to the concentration of 20 mg mL\\u22121 and was stirred for 60 min. Triton X-100 was added to the PCBM solution with different weight percentages with respect to PCBM (1, 3, and 5 wt%) and stirred for 60 min. The homogeneously mixed surfactant-modified PCBM (s-PCBM) solution was filtered using a polytetrafluoroethylene (PTFE) filter (pore size: 0.45 \\u03bcm) and used as an electron transport material for perovskite solar cells.\\n\\nThe PSCs were fabricated on patterned, fluorine-doped tin oxide (FTO)-coated glass with a sheet resistance of 15 \\u03a9 sq\\u22121 (Pilkington). FTO substrates were cleaned sequentially in deionized (DI) water, acetone, and 2-propanol for 60 min using an ultra-sonication bath. A NiOX hole transport layer (HTL) was deposited by spin-coating a NiOX nanocrystal (NC) dispersion solution at 3000 rpm. NiOX NCs were synthesized according to the procedures reported elsewhere. Briefly, 0.05 mol of nickel nitrate hexahydrate (Ni(NO3)2\\u00b76H2O) was dispersed in 20 mL of DI water. Then 6 mL of NaOH solution (10 mol L\\u22121) was slowly dropped into the solution to obtain a large amount of precipitation and stirred for 30 min. The precipitate was washed with deionized water three times, and dried at 80 \\u00b0C. The obtained cyan powder was then calcined at 300 \\u00b0C for 2 h (ramping rate: 5 \\u00b0C min\\u22121) to produce a black NiOX powder. The obtained NiOX NCs were dispersed in DI water to 15 mg ml\\u22121 concentration. A perovskite precursor solution was prepared by dissolving 172 mg of FAI, 22 mg of MABr, 507 mg of PbI2, and 73 mg of PbBr2 in 1 mL of DMF\\\\/DMSO (v\\\\/v = 4\\\\/1) mixed solvent, and stirred at 60 \\u00b0C. The perovskite precursor solution was spun-cast at 1000 rpm for 10 s and 5000 rpm for 25 s on the pre-heated substrate at 40 \\u00b0C, under a N2 atmosphere. During the second spin-coating step, 0.3 mL of chlorobenzene was dripped onto the center of the substrate to promote perovskite film crystallization. After the whole spin-coating process, the substrate was annealed at 100 \\u00b0C for 20 min to form FA0.83MA0.17Pb(I0.83Br0.17)3 films. The electron transport layer was spin-coated from a PCBM solution (20 mg mL\\u22121 in chlorobenzene) or as-prepared s-PCBM solution at 3000 rpm for 30 s. Finally, a 60 nm-thick Au electrode was deposited by thermal evaporation. The active area of the fabricated device was 0.09 cm2.\\nFor PEDOT:PSS-based PSCs, a HTL was formed by spin-coating a PEDOT:PSS aqueous solution at 5000 rpm on a FTO substrate, and annealed at 125 \\u00b0C for 20 min. Further fabrication procedures were the same as those for the NiOX-based PSCs.\\n\\nAtomic force microscopy (AFM) images were acquired using an Park NX10 (Park Systems) and analyzed with XEI AFM data analysis software. Transmission electron microscopy (TEM) images were obtained using a JEM 2100 (JEOL). Field-emission scanning electron microscopy (FE-SEM) images were obtained using a JSM-6701F (JEOL). Photoluminescence spectra of the perovskite samples were recorded using an LS 45 fluorescence spectrometer (PerkinElmer, USA). Electrochemical impedance spectra (EIS) of the devices were measured by Zive Labs (Wonatech). The J\\u2013V characteristics of the devices were measured using an I\\u2013V tracer (MP-160, Eko Instruments) under standard AM 1.5G (100 mW cm\\u22122) illumination from a 500 W xenon lamp, calibrated with a KG5-filtered Si reference cell (K801, McScience Inc.). The external quantum efficiency (EQE) was acquired from 350 nm to 850 nm using a K3100 IPCE Measurement System (McScience Inc; chopping frequency of 4 Hz, without bias light and 10 nm step wavelength).\\n\\n\",\r\n    \"Methylammonium iodide (CH3NH3I) was synthesized and purified based on the method proposed by J. H. Im. All chemicals were used as received. Methylammonium iodide (CH3NH3I) was synthesized by mixing methylamine (CH3NH2) (27.8 mL, 0.273 mol, 40 wt% in methanol, Alfa Aesar) and hydroiodic acid (HI) (30 mL, 0.227 mol, 57 wt% in water, Alfa Aesar) in a 250 mL round-bottom flask, and stirring the mixture in an ice-water bath for 2 h. The yellowish raw product obtained by evaporating the solvent was recrystallized three times from a mixture of diethyl ether and ethanol. After filtration, the solid was collected in a dark container and dried at 60 \\u00b0C in a vacuum oven overnight. Anhydrous EuI2 was synthesized and purified based on the method proposed by Chengpeng D. Anhydrous EuI2 was prepared by dissolving europium oxide (Eu2O3) and ammonium iodide (NH4I) into HI to form a transparent solution. We obtained a dense solid after we evaporated the solution. Then the solid was placed into a quartz tube for vacuum dehydration in a tube heating furnace, until it was completely dehydrated. After that, the dehydrated solid was sintered until the solid turned to transparent melt. Eventually, anhydrous EuI2 in bulk polycrystalline was obtained.\\n\\nDevices were fabricated on fluorine-doped tin oxide (FTO) coated glass (Yingkou OPV Tech New Energy CO., LTD., OPV-FTO22-7). Initially, FTO was etched with 2 mol L\\u22121 HCl solution and zinc metal powder. Substrates were then cleaned sequentially by soap solution (2 vol% Hellmanex\\u2122 detergent), deionized water, acetone, ethanol, isopropanol (IPA) and UV exposure. Nickel(II) acetylacetonate was dissolved in ethanol (0.1 mol L\\u22121) with adding 5.3 \\u03bcL ethanolamine (38 wt%) into the solution. The solution was then stirred in a sealed glass vial in air overnight. Then the NiO solution was spin-coated onto the UV\\u2013ozone treated FTO substrate at 3000 rpm for 60 s and then annealed at 400 \\u00b0C for 60 min in ambient.\\nThe perovskite thin film was deposited by using a process similar to that described in a previous work. The MAPbI3:x% EuI2 (x = 0, 0.02, 0.04, 0.06, 0.08, 0.1) precursor solution was prepared by dissolving CH3NH3I (1 mmol), PbI2 (1.05 mmol; Alfa Aesar, 99.9985%) and EuI2 (a corresponding mass fraction of PbI2) in g-butyrolactone (GBL)\\\\/dimethyl sulfoxide (DMSO) (7:3; 1 mL) with a total concentration of 1 M and stirring at 70 \\u00b0C overnight. The perovskite thin films spread with 80 \\u03bcL was spin coated onto the FTO\\\\/NiO substrate followed by a two-stage spin-coating process at 1000 rpm for 15 s and 4000 rpm for 45 s. Then chlorobenzene (600 \\u03bcL; Alfa Aesar, 99%) was dripped as anti-solvent after 25 s the second stage to obtain a light-brown smooth film. Afterward, the perovskite film was annealed at 100 \\u00b0C for 10 min to convert to a dark-brown film. Subsequently, PCBM (15 mg dissolved in 1 mL chlorobenzene) was deposited on the cooled perovskites substrates by spin coating at 1500 rpm for 45 s, followed by the spin coating of BCP saturated solution in isopropanol. Finally, silver electrode (70 nm thick) was thermally evaporated on top of the device under high vacuum (<1 \\u00d7 10\\u22124 Pa). The active area of the device was 0.090 cm2, defined by the aperture area of the metal shadow mask.\\n\\nX-ray diffraction (XRD) patterns were obtained with Smart LAB instruments CuK\\u03b1 beam (\\u03bb = 1.54 \\u00c5). UV-vis absorption spectra measurement was carried out on a Hitachi U-3010 spectroscope, and was employed to assess the absorption properties of the doped perovskite sensitized NiO thin film. The morphology of the film was tested with scanning electron microscopy (SEM; JEOL JSM-7401F). The incident photon-to-electron conversion efficiency (IPCE) spectra were measured in air with equipment developed by the Institute of Physics, Chinese Academy of Sciences.\\nThe energy dispersive X-ray spectroscope (EDS) combined with a field-emission scanning electron microscope (SEM-EDS, EDAX Octane Pro). X-ray energies corresponded to I, Pb and Eu were collected as the SEM scanned the electron beam over the surface and cross-sectional area in FTO substrate. The X-ray data was synchronized with the SEM image and an \\u2018element image\\u2019 was created showing the presence of the selected element throughout the selected area.\\nThe current density\\u2013voltage (J\\u2013V) curves were measured with a 2400 Series SourceMeter (Keithley Instruments) under simulated AM 1.5 sunlight at an equivalent to 100 mW cm\\u22122 irradiance generated by an thermo oriel 91192-1000 simulator, with the intensity being calibrated with an VLSI standards incorporated PN 91150V Si reference cell. The mismatch factor was calculated to be less than 1%. The solar cells were masked with a metal aperture to define the active area, typically 0.090 cm2. The backward bias for stability characterization of the solar cell was held to 0.75 V. The as-prepared solar cells were stored at 25 \\u00b0C in light with a relative humidity (RH) of 30 \\u00b1 5% for the characterization of ambience stability. The specific PCE as a function of time was obtained with conventional environment treatment for 13 days in order to clarify the PCE evolution of solar cells.\\n\\n\",\r\n    \"All chemicals were used as received without purification, including PbI2 (99.9985%, Alfa Aesar), CH3NH2 (40 wt% aqueous solution, J&K Scientific), HI (57% w\\\\/w aqueous solution, Alfa Aesar), C60 (99.5%, HanFeng Chemical), [6,6]-phenyl-C61-butyric acid methyl ester (PCBM, 99%, Solenne BV), 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP, >99%, P-OLED), dimethylformamide (DMF, 99.9%, J&K Scientific), 1,2-dichlorobenzene (98%, Alfa Aesar) and poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS, P VP. Al 4083, Heraeus). The sheet resistance of ITO (170 nm in thickness) was 11 \\u03a9 per square.\\nMethylammonium iodide (MAI) was synthesized by reacting 16 mL of CH3NH2 solution and 10 mL of HI solution in a 3-necked 100 mL round-bottom flask filled with argon at 0 \\u00b0C for 2 h with stirring. The solvent was removed using a rotary evaporator at 50 \\u00b0C. The pale yellow precipitate was recrystallized with ethanol twice, filtered and washed with enough ethyl ether to remove the yellow by-product. The white product was dried at 60 \\u00b0C in a vacuum oven for 24 h, weighed and stored in an argon-filled glove box before use.\\n\\nWe used Zn powder and concentrated HCl to pattern the ITO substrates. The part to be remained was covered with tapes during etching. The patterned ITO substrates were first ultrasonically cleaned in detergent, rubbed using cotton, and then rinsed with distilled water. After drying, the surface of ITO was treated under UV\\\\/O3 for 15 min.\\nThe PEDOT:PSS aqueous solution was filtered with a 0.45 \\u03bcm PVDF membrane before spin coating. PEDOT:PSS films with a thickness of 40 nm were spin-coated onto the ITO substrates at 3000 rpm for 60 s. The substrates were baked on a 120 \\u00b0C hot plate in air for 20 min. PbI2 (0.368 g) was dissolved in 1 mL of DMF, into which about 18.9 \\u03bcL of water was added. The mixture was stirred for 5 h on a 70 \\u00b0C hot plate, and then filtered with a 0.22 \\u03bcm nylon membrane before spin coating. PbI2 films with a thickness of 95 nm were spin-coated onto the PEDOT:PSS or ITO substrates, which were preheated to 50 \\u00b0C, at 8000 rpm for 30 s. The substrates were then baked on a 70 \\u00b0C hot plate in air for 10 min before being transferred onto the bottom plate maintained at 70 \\u00b0C.\\nFive milligrams of MAI powder was dissolved in 10 mL of ethanol. Then the solution was homogeneously sprayed onto the bottom surface of the top plate that was maintained at 80 \\u00b0C. The distance between the plate and nozzle was about 10 cm and the pressure of compressed air used for spraying was about 1.5 atm. Then the top plate was placed on top of the bottom plate in the desiccator.\\nThe PHP apparatus was then sealed and pumped down to a pressure of about 100 Pa. At the same time, the top and bottom plates were ramped up to nominal temperatures of 120 \\u00b0C and 130 \\u00b0C, respectively. The plates were maintained at the temperatures for desired times before refilling the apparatus with Ar.\\nPCBM films with a thickness of 20 nm were spin-coated with a PCBM solution in dichlorobenzene (26 mg mL\\u22121) onto the perovskite films at 2400 rpm for 30 s, and annealed at 110 \\u00b0C for 10 min in air. Then the films were transported into a glove box filled with Ar, in which C60 (20 nm, 0.1 nm s\\u22121), BCP (8 nm, 0.01 nm s\\u22121) and Al (150 nm, 1 nm s\\u22121) were deposited in sequence by thermal evaporation under a background pressure of about 1 \\u00d7 10\\u22125 Pa.\\n\\nMorphology and elemental analysis of films were investigated using a cold field emission scanning electron microscope (SEM, SU8010, Hitachi) equipped with an IXRF energy dispersive spectroscopy (EDS) system. Data were acquired with an accelerating voltage of 15 kV for the latter. X-ray emissions of Pb M\\u03b11 and I L\\u03b11 at 2.3455 keV and 3.9376 keV respectively are chosen for analysis. We chose Pb M\\u03b11 emission instead of Pb L\\u03b11 emission (at 10.5515 keV) because of the stronger peak intensity of the former. The measured atomic ratios of I\\\\/Pb were calibrated with that of PbI2, which is 2:1. UV-visible absorption of perovskite films in VSR was recorded with a UV-vis spectrometer (U-4100, Hitachi). X-ray diffraction (XRD) patterns of films were recorded using an X-ray diffractometer (Rigaku D\\\\/MAX 2500) with Cu K\\u03b1 radiation at 5\\u00b0 per min from 10\\u00b0 to 60\\u00b0. The local irradiance on the films under reaction was measured with a radiometer (FZ-A). The thicknesses of films and widths of channels were measured with a profiler (AlphaStep D-100).\\nCurrent density\\u2013voltage (J\\u2013V) curves were measured with a programmed Keithley 2400 sourcemeter under illumination of a Newport Oriel 150 W solar simulator (AM 1.5 G, 100 mW cm\\u22122). All tests were carried out in air without encapsulation. The light intensity of the solar simulator was calibrated with a solar reference cell (SRC-1000-TC-QZ, VLSI standards, Inc.). The scanning step and sweeping rate of bias were 10 mV and 0.2 V s\\u22121, respectively.\\n\\nFor the electrical resistance measurements, a channel about 250 \\u03bcm in width was first etched along the diagonal of an ITO substrate. We connected the edges of the ITO substrate with the external circuit using copper powder conductive paste. The PEDOT:PSS aqueous solution was diluted with water (10 V\\\\/V%) and then filtered with a 0.45 \\u03bcm PVDF membrane. PEDOT:PSS films were spin-coated onto the ITO substrates at 3000 rpm for 30 s. Afterwards, similar fabrication procedures were used except that the resistance of the films during the reaction was monitored in situ with a UT61E multimeter, which was connected to a computer for data recording (Fig. 7b).\\n\\n\",\r\n    \"20 mL of hydroiodic acid (57 wt% in H2O) was added dropwise to 48 mL methanol (40 wt%) under ice bath stirring for 2 h. The reactant solution was distilled in a rotary evaporator at 55 \\u00b0C to remove the solvents, and then the precipitate was washed by diethyl ether 3 times. Finally, a white-colored powder was collected and dried at 60 \\u00b0C for 24 h under vacuum. The mixture of PbCl2:CH3NH3I with a 1:3 molar ratio was dissolved in DMF and then stirred at 60 \\u00b0C overnight, giving the perovskite precursor solution.\\n\\nThe used device structure is shown in Fig. 1(a). ITO-coated glass substrates (15 \\u03a9 sq\\u22121) were ultrasonically-coated in acetone and ethanol at room temperature for 15 min, then UV-Ozone cleaner for 15 min. A film (45 nm thick) of PEDOT:PSS was spin-coated onto the ITO substrate at 4500 rpm and annealed at 140 \\u00b0C for 10 min. Then, the prepared perovskite precursor solution was spin-coated at 4000 rpm. For the thermal annealing process, the perovskite films were conducted by a typical gradient increased temperature method (the films were slowly heated from 60 to 100 \\u00b0C at a rate of 10 \\u00b0C\\\\/10 min on a hot plate). For the EEF assisted annealing process, EEFs were exerted on the perovskite films using a conductive glass cover, where a spacing of about 60\\u201380 \\u03bcm was set [Fig. S1(a)\\u2020]. To acquire the spacing, we put a plastic strip between two of the same conductive substrates to build a similar flat capacitor with air as the dielectric. Using C = \\u03b5A\\\\/d, the spacing can be deduced by measuring the capacitance. The electric field intensity (E) can be obtained based on E = V\\\\/d, where V is the applied DC voltage (60 V or 150 V). During the cooling process from 100 \\u00b0C to room temperature, the EEF was kept constant, and the photo taken during the EEF assisted annealing treatment is shown in Fig. S1(b).\\u2020 A PCBM layer was deposited from a 20 mg mL\\u22121 chlorobenzene solution at 2000 rpm. Then 0.5 mg mL\\u22121 Bphen in absolute ethanol was coated onto a PCBM layer at 4000 rpm. Finally, 100 nm thick Ag (mask area of 0.0725 cm2) was deposited on top of the Bphen layer by thermal evaporation under 10\\u22127 Torr.\\n\\nJ\\u2013V characteristics of the PSCs were recorded under 1 sun illumination using a programmable Keithley 2400 source meter under AM 1.5G simulated solar light. Incident photon current efficiency (IPCE) was measured by a 1000 W halogen lamp and grating monochromator (Acton Spectra Pro 2300i). Electrical impedance spectroscopy (EIS) and Mott\\u2013Schottky capacitance analysis were surveyed by Ivium (Netherlands). The absorption spectra were measured with a UV\\\\/vis spectrophotometer (PerkinElmer Lambda 750). The surface morphology and element distribution in energy dispersive X-ray (EDX) were characterized by scanning electron microscopy (SEM, Quanta 200 FEG, FEI Co.). X-ray diffraction (XRD) patterns were measured using PANalytica 80 equipment (Empyrean, Cu K\\u03b1 radiation with a wavelength of 0.154 nm). 2D-GIXRD patterns were obtained by a MarCCD 225 detector mounted vertically at a distance of around 256.401 mm from the sample with an exposure time of 100 s at a grazing incidence angle of 0.2\\u00b0. The coordinates of the GIXRD patterns were represented by diffraction vectors with q = 4\\u03c0sin(\\u03b8)\\\\/\\u03bb, where \\u03b8 is half of the diffraction angle and \\u03bb is the wavelength of the incident X-ray. P\\u2013E loops were tested by PMF0312-295 (Radiant Technologies, USA). The dielectric spectra were tested by a Precision Impedance Analyzer (Agilent 4294A).\\nKelvin Probe Force Microscopy (KPFM) is tested by PMF0312-295 (Radiant Technologies, USA), which is based on Atomic Force Microscopy (AFM) (Fig. S7(g) in the ESI\\u2020). Firstly, the surface topography is mapped in the tapping mode. Secondly, the contact potential difference (CPD) between the AFM tip and the sample is detected by retracing at a left height from the sample surface. During the second test procedure, a compensated DC voltage is applied to offset the potential difference between the tip and sample. Therefore, local potential distribution on the sample surface is observed, and the work function of the sample is obtained if the tip\\u2019s work function is known. All measurements are taken in air conditions.\\n\\n\",\r\n    \"Methylamine solution (40 wt% in ethanol), hydriodic acid (57 wt% in H2O) and lead(II) iodide (PbI2, 99.999%) were purchased from Alfa or Sigma-Aldrich. Phenyl-C61-butyric acid methyl ester (PCBM) was obtained from Solarmer Materials Inc. Methylammonium iodide (MAI) was synthesized according to the literature by stoichiometrically reacting methylamine with hydriodic acid. The perovskite precursor was prepared by mixing MAI and PbI2 in a molar ratio of 1:1 in anhydrous N,N-dimethylformamide (DMF, 99.8%, Alfa), and the final concentration of the perovskite was controlled to approximately 40 wt%. The solution was stirred overnight at room temperature and filtered with 0.45 \\u03bcm PVDF filters before spin-coating. The synthesis and characterization of PDINO were reported elsewhere.\\nFirst, the patterned ITO substrates were sequentially ultrasonically cleaned with detergent, deionized water, acetone and isopropanol. On the cleaned ITO substrate, the PEDOT:PSS aqueous solution filtered through 0.45 \\u03bcm PVDF filters was spin-coated at 4000 rpm for 30 s and then dried at room-temperature in air. The as-prepared perovskite precursor solution was spin coated onto the ITO\\\\/PEDOT:PSS substrate at a speed of 5000 rpm for 30 s. During the last 4.5 s of the spinning process, chlorobenzene was quickly added to induce fast crystallization. Then the perovskite film was treated by air, TA or WVA methods under the following treatment conditions: (1) air treatment. The sample plates of the spin-coated perovskite films were placed at room temperature in air (25 \\u00b0C, RH% < 10%). (2) TA treatment. As a control, the TA process was conducted by putting the sample plates on a hot plate maintained at 100 \\u00b0C for 10 minutes in air (RH% < 10%). (3) WVA treatment. The sample plates of the spin-coated perovskite films were put in Petri dishes (with a cover but not sealed) with vapors of water with different volumes and different duration times. The treatment was performed at room temperature in air (25 \\u00b0C, RH% < 10%). After the WVA or TA treatments, the PCBM (20 mg mL\\u22121 in chlorobenzene) and PDINO (1 mg mL\\u22121 in methanol) were then sequentially deposited by spin coating at 1500 rpm for 30 s and 3000 rpm for 30 s, respectively. Finally, a 100 nm Al electrode was deposited on the PDINO layer under high vacuum by thermal evaporation.\\nThe current density\\u2013voltage (J\\u2013V) characteristics were measured on a computer \\u2013 controlled Keithley 2450 Source \\u2013 Measure Unit. An Oriel Sol3A Class AAA Solar Simulator (model, Newport 94023A) with a 450 W xenon lamp and an air mass (AM) 1.5 filter was used as the light source. The input bias voltage was scanned in forward (\\u22121.5 V to 1.5 V, FS) and reverse directions (1.5 V to \\u22121.5 V, RS) in 0.01 V steps with a scan rate of 0.1 V s\\u22121. The measurement was through a shadow mask with an active area of 0.05 cm2 under illumination at ca. 25.0 \\u00b0C. The light intensity was calibrated to 100 mW cm\\u22122 by using a Newport Oriel 91150V reference cell. The EQE spectra were recorded with an Enli Technology (Taiwan) EQE measurement system (QE-R), and the light intensity at each wavelength was calibrated with a standard single-crystal Si photovoltaic cell. The thickness of the interlayer was determined by using a Profilometer (Ambios Tech. XP-2). Scanning electron microscopy (SEM) was performed in order to investigate the morphology of the perovskite films prepared on top of PEDOT:PSS. Top-view and cross-sectional images were characterized by using a HITACHI s-4800 (Hitachi Limited, Japan) using an InLens detector operating at an accelerating voltage of 10 kV. The atomic force microscopy (AFM) images were obtained by utilizing a SPA-400 SPM (Seiko Instrument, Inc.). The X-ray diffraction (XRD) patterns were recorded on a D\\\\/MAX-2000 X-ray diffractometer with monochromated Cu K\\u03b1 irradiation (\\u03bb = 1.5418 \\u00c5). The time-resolved PL measurements at the peak emission of \\u223c765 nm were recorded by using a lifetime and steady state spectrometer (FLS980, Edinburgh Instruments Ltd.) with a 470 nm laser.\\n\",\r\n    \"PBDTT-DPP polymer & PFN, PCBM and PC70BM were purchased from 1-Material Inc., Solarmer Materials Inc. and Nano-C, respectively. CH3NH3I was synthesized by following the reported procedure. PbCl2 (Aldrich) and CH3NH3I were mixed in DMF or the DMF\\\\/DMSO (0.8:0.2 in Volume) solution at a molar ratio of 1:3 with different weight percentages.\\n\\nITO coated glass slides were cleaned by ultra-sonication for 30 minutes in detergent water, de-ionized water, acetone and ethanol, sequentially. The ITO substrates were then subjected to UVO treatment for 25 minutes. The PEDOT:PSS layer were spin-coated onto the ITO substrates. For the single-junction planar PVSK solar cells, the precursor in mixed DMF\\\\/DMSO solvent (60 wt%) was spin-coated onto the PEDOT:PSS layer. As a reference, the precursor in DMF solvent (60 wt%) was also spin-coated onto a PEDOT:PSS layer. The obtained films were subjected to low-temperature (60 \\u00b0C) annealing under vacuum for 40 minutes in order to remove the solvent. Then, the sequential films were annealed at 80 \\u00b0C for one hour to transfer the PVSK layers with a thickness of 220 nm. Then, the 40 nm thick PCBM layer was deposited onto the PVSK layer as a n-type layer and a PFN film with a thickness of 1 nm was spin-coated as an interfacial layer. Finally, a 80 nm thick Ag was thermally deposited as the cathode. For single-junction organic solar cells, the PBDTT-DPP\\\\/PC70BM blended solution (1:2, 18 mg ml\\u22121 in 1,2-dichlorobenzene o-DCB) was spin-coated onto the PEDOT:PSS layer to form a 110 nm thick layer. Ca (20 nm)\\\\/Al (100 nm) were sequentially thermal-evaporated as the cathode. The area of the cells was 0.06 cm2 as defined by the mask.\\n\\nThe fabrication of the front sub-cell mainly followed the procedure for the preparation of the single-junction device until the Ag cathode was deposited. The only difference was the variation of the PVSK layer thickness for optimization of the tandem devices. Sequentially, the Ag or Al doped MoO3\\\\/MoO3 bi-layer was deposited as an ICL, where the co-evaporation technique was used for the doped-MoO3 layer deposition. The content of Al in MoO3\\u2013Al step layer was kept between 40 and 50 wt%. The PBDTT-DPP\\\\/PC70BM blended solution (1:2, 18 mg ml\\u22121 in 1,2-dichlorobenzene o-DCB) was spin-coated onto the PEDOT:PSS layer to form a 110 nm thick layer. Ca (20 nm)\\\\/Al (100 nm) were sequentially thermal-evaporated as the cathode. The area of the cells was 0.06 cm2 as defined by the mask.\\n\\nThe work functions of different layers were measured by a Kelvin probe. The morphology of the PVSK layers on ITO\\\\/PEDOT:PSS substrates were characterized by scanning electron microscopy (SEM, Hitachi S-4800). The refractive index (n and k values) of the layers in the device structure was measured using a VASE ellipsometer from J. A. Woollam Co., Inc. Current density\\u2013voltage (J\\u2013V) characteristics were obtained by using a Keithley 2635 source meter and Newport AM 1.5G solar simulator with irradiation intensity of 100 mW cm\\u22122. The thicknesses of the layers were measured by a Dekak Stylus Profiler.\\n\\n\",\r\n    \"Glass\\\\/ITO and PET\\\\/ITO substrates were purchased from Advanced Electronic Technology Co., Ltd. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), phenyl-C61-butyric acid methyl ester (PC61BM), and 4-tert-butylpyridine (tBP) were supplied by Xi\\u2019an Polymer Light Technology Corporation. CH3NH3I (MAI) and PbI2 were purchased from Kunshan Sunlaite New Energy Technology Co., Ltd. Other materials were purchased from Aladdin.\\n\\nInverted-planar p\\u2013i\\u2013n perovskite solar cells (PSCs) were fabricated on laser-patterned, indium tin oxide (ITO) coated glass (rigid) and PET (flexible) (10 \\u03a9 sq\\u22121) substrates, respectively. Both of them were sequentially cleaned by ultra-sonication with deionised water, acetone, ethyl alcohol, and isopropyl alcohol (IPA) for about 15 min and then dried at high-temperature with clean dry nitrogen. After cleaning, the substrates were treated with ultraviolet (UV) ozone for 20 min to enhance the surface wettability. For the proposed cryo-controlled quasi-congealing spin-coating, low temperature (\\u223c5 \\u00b0C) PEDOT:PSS aqueous solution (with small amounts of DMSO) was spin-coated on the clean substrate at 0 \\u00b0C at 5000 rpm for 30 s, and then annealed at 120 \\u00b0C for 1 h. Detailed illustrations and mechanism of this technique are clearly described in the following section. The moisture-resistant CH3NH3PbI3\\u00b7xtBP was produced by two-step spin-coating. Firstly, the PbI2 precursor (1.2 M, dissolved in DMF and stirred for 1 h at 70 \\u00b0C) with 40 \\u03bcL mL\\u22121 of tBP was spin-coated on the PEDOT:PSS substrate at 4500 rpm for 30 s and dried at 70 \\u00b0C for 15 min. After the formation of PbI2\\u00b7xtBP, CH3NH3I (12 mg mL\\u22121, dissolved in the IPA solvent) was continuously spin-coated at 4000 rpm for 30 s to form CH3NH3PbI3\\u00b7xtBP and annealed at 100 \\u00b0C for 1 h. For the electron-transport layer (ETL), PC61BM (20 mg mL\\u22121 in chlorobenzene) was spin-coated on top of the perovskite layer at 2000 rpm for 30 s and annealed at 80 \\u00b0C for 1 h. The fabrication was completed by thermal evaporation of Ag as an electrode with a thickness of approximately 100 nm and an effective area of 0.06 cm2. The whole fabrication could be performed well in a high humidity environment (RH > 40%), which shows that the use of a glove box is not necessary. The fabrication process is illustrated in Fig. S1 (ESI\\u2020).\\n\\nThe photocurrent density\\u2013voltage (J\\u2013V) characteristics of the cells were measured using a Keithley 2400-SCS source meter under AM 1.5 illumination with an intensity of 100 mW cm\\u22122. The crystal structures of PbI2 and MAPbI3 were analysed by X-ray diffraction (XRD, Thermo ARL-X\\u2019TRA, America) with Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5). Field-emission scanning electron microscopy (FESEM, Ultra55, ZEISS, Germany) and atomic force microscopy (AFM, XEI-100E) were employed to analyse the morphologies. The incident photon-to-current conversion efficiencies (IPCEs) of the cells were measured with a quantum-efficiency (QE)\\\\/IPCE test system (Solar Cell Scan100\\\\/Zolix). Electrochemical impedance spectroscopy (EIS) measurements were carried out using an electrochemical workstation (Zennium Pro, Germany). The steady-state and time-resolved photoluminescence (TRPL) spectra were measured by using a PG2000-Pro-EX spectrophotometer (Shanghai Ideaoptics Corporation) and a transient fluorescence spectrometer (FLS980, Edinburgh Instruments, EI), respectively. The contact properties were characterised using a contact-angle instrument (Kr\\u00fcss Optronic, Germany). The UV-visible (UV-vis) absorption was measured using a UV-vis spectrophotometer (Lambda 900, America).\\n\\n\",\r\n    \"All reagent grade chemicals were obtained commercially from Sigma-Aldrich, St Louis, MO, unless noted otherwise. MAI was prepared in-house. In a typical procedure, 24 ml of a 33 wt% methylamine (CH3NH2) solution in anhydrous ethanol was reacted with 10 ml of 57 wt% hydroiodic acid (HI) in water, in 100 ml of ethanol (excess CH3NH2) in a dry Ar atmosphere at room temperature. The solvent and excess CH3NH2 were removed using a rotary evaporator, and the resulting MAI powder was harvested.\\n\\nFirst, a 0.8 M PbI2 (Alfa-Aesar, Ward Hill, MA) solution in N,N\\u2032-dimethylformamide (DMF) was spin-coated onto different substrates: plain glass, quartz, previously patterned fluorine-doped tin oxide (FTO) coated glass (TEC15, Hartford Glass Co., Hartford City, IN), or the patterned FTO-coated glass with a TiO2 blocking layer (\\u223c15 nm). A smooth, nanoporous PbI2 thin film was formed, which was then dried at room temperature under blowing air. Second, a fresh MAI solution of 10 mg ml\\u22121 in anhydrous isopropanol was spin-coated onto the as-prepared PbI2 layer immediately, and was then annealed at 150 \\u00b0C for 1 min, which constitutes the first SSCA cycle. This SSCA cycle was then repeated 3 to 4 times. The excess MAI was washed with isopropanol, and the final thin films were annealed at 150 \\u00b0C for 2 min to obtain a dark-colored perovskite film. The film thickness can be controlled by the spinning conditions. The spin-coating conditions of 4000 rpm for 15 s was used for all thin film depositions, which resulted in 250\\u2013300 nm MAPbI3 perovskite thin films. The nature of the substrate (plain glass, quartz, FTO-coated glass, and FTO-coated glass with a TiO2 blocking layer) did not have any obvious effects on the SSCA-processed MAPbI3 perovskite films.\\n\\nFor the fabrication of the PSCs, the FTO-coated glass was patterned by 25% hydrochloric acid etching with zinc powder, and cleaned by soaking in a base bath (5 wt% NaOH in ethanol) overnight. After washing with deionized water and ethanol, a compact TiO2 blocking layer was deposited on top of the patterned FTO by spray pyrolysis at 450 \\u00b0C. The perovskite layer was then deposited using the SSCA process (one, two or three SSCA cycles), as described above. This was followed by spin-coating a solution of a HTM, which consisted of 80 mg 2,2\\u2032,7,7\\u2032-tetrakis(N,N-dip-methoxyphenylamine)-9,9\\u2032-spirobifluorene (Spiro-MeOTAD; Merck, Germany), 30 \\u03bcl bis(trifluoromethane) sulfonimide lithium salt stock solution (500 mg Li-TFSI in 1 ml acetonitrile), 30 \\u03bcl 4-tert-butylpyridine (TBP), and 1 ml chlorobenzene solvent. The HTM spin-coating process was performed in a dry-air atmosphere with less than 10% humidity. Finally a 150 nm Ag layer was deposited using a thermal evaporator and a shadow mask. The PSCs were stored in a dry-air atmosphere with a humidity below 5%, and the performance of the PSC was typically measured one day after their fabrication.\\n\\nX-ray diffraction (XRD) was performed on a X-ray diffractometer (D8-Advance, Bruker, Germany) using Cu K\\u03b11 radiation (\\u03bb = 1.5406 \\u00c5) at step size\\\\/time of 0.02\\u00b0\\\\/1 s. The surface morphology of the films was observed by scanning electron microscopy (SEM; LEO 1530VP, Carl Zeiss, Germany). The local roughness of the MAPbI3 thin films were characterized by atomic force microscopy (AFM; 5500, Agilent, Santa Clara, CA) operated in contact mode. Optical spectroscopy (transmission, refection, absorption) of the films on quartz at each formation stage was conducted on a spectral response measurement system (QEXL, PV Measurements, Boulder, CO). Transmission electron microscopy (TEM) was used to characterize cross-sections of the whole PSCs. Note that this particular PSC has a thinner HTM layer compared to most of the other PSCs fabricated in this study. The samples from specific locations on the cross-sections were prepared by focused ion beam (FIB; Helios 600, FEI, Hillisboro, OR) and in situ lift-out. The TEM specimens were examined by TEM (2100F, JEOL, Tokyo, Japan) operated at a 200 kV accelerating voltage.\\n\\nThe incident external quantum efficiency (EQE) spectra of the PSCs were recorded at a chopping frequency of 5 Hz in AC mode on a solar cell quantum efficiency measurement system (QEX10, PV Measurements, Boulder, CO). The current density (J)\\u2013voltage (V) characteristics of the PSCs were obtained using a 2400 SourceMeter (Keithley, Cleveland, OH) under simulated one-sun AM 1.5G illumination (100 mW cm\\u22122) (Oriel Sol3A Class AAA Solar Simulator, Newport Corporation, Irvine, CA). A typical J\\u2013V scan starts from a forward-bias to a short-circuit at a rate of 20 mV s\\u22121. A typical active area of 0.12 cm2 was defined using a non-reflective mask for the J\\u2013V measurements. The steady-state maximum power output of the solar cells was measured by monitoring the current density (J) output at the maximum power voltage (V) bias for up to 300 s using a VersaSTAT MC potentiostat (Princeton Applied Research, Acton, MA). The current output can be converted to a power conversion efficiency (PCE) output using the following equation: PCE = (J (mA cm\\u22122) \\u00d7 V (V))\\\\/(100 (mW cm\\u22122)). A shutter was used to switch on and off the one-sun illumination on the cell. Solar-cell testing was conducted in the ambient atmosphere with a humidity of 20\\u201340%. Impedance spectroscopy (IS) on the PSCs was performed using a PARSTAT 2273 workstation (Princeton Applied Research, Acton, MA) with the frequency range of 0.1 Hz\\u2013100 kHz and the modulation amplitude of 10 mV. The IS spectra were analyzed using ZView 2.9c software (Scribner Associates, Southern Pines, NC).\\n\\n\",\r\n    \"The solar cells have been prepared following a recently described method. In brief MAPbI3 was prepared by a two-step spin coating procedure. The PbI2 layer was first deposited on the mesoporous TiO2 film deposited fluorine-doped tin oxide (FTO) conductive glass, which was followed by coating the MAI solution. The MAPbI3 layer was finally annealed at 100 \\u00b0C for 5 min. Spiro-MeOTAD was spin-coated on the MAPbI3 layer and Au was finally deposited on the spiro-MeOTAD. Incomplete cells with three different MAI concentrations (0.032 M, 0.044 M and 0.063 M) without HTL and Au electrode were also analysed. The preparation procedures were kept identical to the complete devices.\\n\\nThe solar simulator used is equipped with a 1000 W xenon short arc lamp and a Keithley 2651A source meter. The light intensity was calibrated through a Si reference cell in order to give a 1 sun light intensity according to the AM 1.5 G spectrum (class A, AM 1.5 G deviation <2%). No spectral mismatch correction was applied. For efficiency measurements, the cells were equipped with a non-reflective black mask which defined a 0.16 cm2 active area (out of the total active area size of \\u223c0.5 cm2). The scan direction was from the starting voltage of 1.2 V towards the final point at \\u22120.1 V with a 20 mV voltage step and 200 ms time interval between each step. For each typology 3\\u20135 cells were measured giving average conversion efficiency and standard deviation of 7.87 \\u00b1 1.31%, 17.07 \\u00b1 0.31%, 12.03 \\u00b1 0.58% for 0.032 M, 0.044 M and 0.063 M, respectively. The largest standard deviation for 0.032 M devices is also representative for the stronger non-uniformity of the perovskite layer. Out of the 3\\u20135 samples for every cell typology, one device was chosen for the complete characterization (I\\u2013V sun, I\\u2013V dark, VOCvs. light intensity, EL- and PL-imaging and \\u03bc-LBIC) and the corresponding results shown.\\n\\nThe investigation of surface and cross sections of the TiO2\\\\/perovskite films was carried out through a Schottky emission scanning electron microscope SEM (Hitachi, SU-70).\\n\\nThe experimental PL setup consists of a cooled 1 MP Silicon CCD camera, a spatially homogeneous excitation light in the whole active area of the cell (\\u223c0.5 cm2) with about 1.2 Sun light intensity obtained by a 2 halogen-lamp-system filtered by a 650 nm dielectric short-pass filter and an absorption band-pass filter with a transmittance of 500\\u2013900 nm. A power source and a stack of optical filters between the camera and the sample completed the equipment. The filter stack of the camera lens was composed of a 725 nm dielectric long-pass and an absorption long-pass with a smooth edge from 720 nm to 760 nm in order to obtain a sufficient suppression of excitation light incident on the camera. Furthermore a short pass filter is put in front of the camera filter stack to suppress light above 900 nm. The operating point of the cell was changed through the power source from VOC to 0 V. PL images were acquired with 50\\u2013100 mV voltage steps (smaller voltage steps close to VOC were used to better follow the steep I\\u2013V curve behaviour in this range). For every step an equilibration time of 2 s was used. Integration time was in the range 0.1\\u20130.5 s per image. The spatial resolution was about 40 \\u03bcm per camera pixel. The EL setup shared the same equipment. EL measurements were performed in the dark by application of a forward bias voltage. The filter stack was removed since no filtering of excitation light was necessary. The operating point of the cell was changed from 800 mV to 1300 mV with 50 mV voltage steps while EL images were acquired. Integration time was changed as a function of the operating point from 60 s to 0.5 s in order to get a high signal-to-noise ratio. It was observed that the prolonged application of high voltages during EL measurements reversibly modified the electrical characteristics of the cell. In particular, the current at a fixed high voltage was seen to decrease. A similar behaviour was also observed on the PL intensity (decrease) with light exposure. Following equilibrium conditions, the original parameters were restored within tens of seconds. A short integration time was used for PL and EL in order to minimize the device perturbation. Moreover, a recovery time of 60 s was taken between every step to avoid overheating of the device (in case of PL) and permit a complete device re-equilibration.\\n\\n\\u03bc-PL and \\u03bc-LBIC (Light Beam Induced Current) allow the investigation of photoluminescence and current generation with a micrometric resolution on the device. The cell is mounted on a movable stage. Excitation is done via a frequency doubled Nd:YAG laser at 532 nm, which is focused on the sample. For the large area \\u03bc-LBIC maps, an objective lens with an NA = 0.26 is used to obtain a low depth of focus. The intensity is set to 1 sun equivalent photon flux of about 7 \\u00d7 1017 cm\\u22123 s\\u22121 and spot size to 20 \\u03bcm in diameter. The induced current is measured by a highly sensitive current preamplifier. Emitted PL is collected with the same lens as is used for excitation, directed towards a grating spectrometer and detected by a silicon line CCD. By so doing the PL spectrum can be detected in the illuminated spot. By raster scanning the sample, the spatial resolution is established which is diffraction limited. For the highly resolved \\u03bc-PL maps an objective lens with numerical aperture of NA = 0.9 is used, which allows for a diffraction limited spot size of 260 nm and a corresponding spatial resolution. Typical integration times are 10 ms\\u2013100 ms per pixel. In complete devices the laser beam was shone from the glass side, meaning that the light passes through the TCO glass till the Au back electrode of the cell. In the case of properties\\u2019 investigation of perovskite crystals, incomplete cells were used (TCO\\\\/compact_TiO2\\\\/mesoporous_TiO2\\\\/perovskite). The high resolution \\u03bc-PL images were carried out with laser excitation from the perovskite crystal side (capping layer side). 3\\u20135 cells for each typology were tested for generating enough statistical data for a robust investigation of \\u03bc-PL\\\\/\\u03bc-LBIC. The resulting differences among samples of similar typology were very small compared to the differences between devices with different MAI concentrations. The cells were stored under dark and in a humidity-free environment throughout the PL\\u2013EL measurement timespan to prevent degradation effects.\\n\\n\",\r\n    \"For the perovskite layer, the MAPbI3 solution was composed of methylammonium lead trihalide (CH3NH3I) and lead(II) iodide (PbI2) in a ratio of 1.06:1 mol%, and it was mixed in gamma-butyrolactone (GBL) and DMSO (7:3 v\\\\/v%) with a molar concentration of 1.4 mol L\\u22121 at 100 \\u00b0C for 4 h. The Clevios P VP AI 4083 type of PEDOT:PSS was purchased from Heraeus (Germany). The PC70BM solution was dissolved in chlorobenzene (CB) in a concentration of 20 mg mL\\u22121.\\n\\nBoth CON-10 and CON-16 suspensions were prepared by dissolving 4 mg of each CON in 1 mL of DMSO with ultrasonication for 30 min.\\n\\nThe inverted perovskite photovoltaic devices were fabricated on a structure consisting of ITO\\\\/(CON)\\\\/PEDOT:PSS\\\\/MAPbI3\\\\/PC70BM\\\\/(TiOx)\\\\/Al. To fabricate the inverted PSC devices, patterned ITO glasses were washed via 20 min sonication in deionized water, acetone, and 2-propanol. After cleaning, the ITO glasses were dried at 100 \\u00b0C and then treated with ultraviolet (UV) ozone for 15 min. The CON solutions were spin-coated onto ITO glasses at 2000 rpm for 40 s and then annealed at 100 \\u00b0C for 5 min. Prior to the PEDOT:PSS coating onto the CON films, the CON films were treated with UV ozone for 5 min. The PEDOT:PSS was then spin-coated onto the ITO substrates or the CON films at 5000 rpm for 40 s. The PEDOT:PSS films were annealed on a hot plate at 140 \\u00b0C for 10 min to generate a thin film with a thickness of 30 nm. The MAPbI3 solution was first spin-coated on a PEDOT:PSS film at 1000 rpm for 30 s and then again at 5000 rpm for 30 s with an additional process of CB drop-casting. Then, the substrates were placed on a hot plate at 100 \\u00b0C for 5 min to fabricate the MAPbI3 film with a thickness of 300 nm. A PC70BM layer with a thickness of \\u223c30 nm was formed on the perovskite layer at 2000 rpm for 40 s. A TiOx interlayer with a thickness of \\u223c10 nm was subsequently added on the active layer at 5000 rpm for 40 s. Finally, an Al cathode was thermally deposited under 4.0 \\u00d7 10\\u22126 Torr with a thickness of \\u223c100 nm using a thermal evaporator. All the devices were encapsulated using a UV-curable resin and a cover glass.\\n\\nThe surface morphologies and roughness of the hole transport and perovskite layers were characterized using the Park NX10 AFM device (Park Systems, South Korea) in the noncontact mode and the SIGMA SEM (Carl Zeiss, Inc., USA) instrument at 5 kV, respectively. In addition, the Bruker-AXS XRD device (Bruker, South Korea) was used to investigate the crystallinity of the perovskite thin films.\\n\\nThe J\\u2013V characteristics of the fabricated inverted OPVs were assessed using the ZIVE SP1 instrument (ZIVE LAB, South Korea) under an AM 1.5-G solar simulator (light and dark conditions). The SCLC and Jph values were measured under the AM 1.5-G solar simulator and the dark condition, respectively. The total cell area of the fabricated inverted PSCs was 0.15 cm2. The IPCE values were measured to prove the short-circuit current of the Jsc. The PL spectra were obtained using the XPERAM 200 Raman microscope (Nanobase, Inc., South Korea). The laser wavelength and the power for each device were 642 nm and 0.3 mW, respectively.\\n\\n\",\r\n    \"For band gap calculations, we firstly obtained the film absorption spectra with a Hitachi U-3010 spectrophotometer in diffusion reflectance mode. Then, the Tauc plot was used to derive band gap values. Since perovskites have direct allowed transitions, we used the following equations for calculation:\\nwhere \\u03b1 is the absorption coefficient, which is derived from the absorption spectra; h is Planck's constant, \\u03bd is the light frequency, and Eg is the band gap. The Tauc plot has a distinct linear regime which denotes the onset of absorption. Then extrapolating this linear region to the abscissa yields the optical band gap.\\n\\nThe clean FTO glasses were used as the substrate for NiMgLiO deposition. The precursor for NiMgLiO was prepared according to the previous reference. In brief, 822.1 mg nickel acetylacetonate, 128.4 mg magnesium acetate tetrahydrate, and 13.2 mg lithium acetate were dissolved in 200 mL of acetonitrile\\\\/ethanol (volume ratio of 95:5) solutions. The film was fabricated by spray coating with FTO as the substrate at 500 \\u00b0C. 30 mL of the above solutions was sprayed using a home-made spray device, with one cycle for 5 seconds (2 seconds for spray, 3 seconds for waiting) and 70 cycles in total. After another 20 min annealing at 500 \\u00b0C in air, the NiO film was fabricated.\\nMAPbI3 perovskite films were fabricated through the following method. Firstly, the precursor solution was prepared by dissolving PbI2 and MAI in a mixed solvent (\\u03b3-butyrolactone:DMSO = 7:3 vol%), with the concentration set to 0.96 M. Then the solutions were coated onto the NiMgLiO film by two consecutive spin-coating steps, at 1500 rpm for 10 s and 5000 rpm for 30 s. During the second step, 0.3 mL chlorobenzene was poured onto the substrate. Then the film was annealed at 90 \\u00b0C for 10 min. Cs0.05FA0.15MA0.8PbI3 films were fabricated using a mixture of CsI, FAI, MAI, and PbI2 in an ideal ratio as the mixed solvent. The concentration was optimized to be 1.2 M. Then the films were annealed at 90 \\u00b0C for 10 min.\\nThen 15 mg mL\\u22121 chlorobenzene solution of PCBM was spin-coated onto the perovskite at 1500 rpm for 30 s, followed by spin-coating of isopropanol solution with saturated BCP at 1500 rpm for 30 s. Finally, a 120 nm Ag electrode was thermally evaporated on top of the device under high vacuum (<10\\u22124 Pa). The active area of the device was 0.16 cm2 with a mask of 0.09 cm2.\\n\\n\",\r\n    \"Unless stated otherwise, all materials were purchased from Sigma-Aldrich and used as received. Poly(bis(4-phenyl)(2,4,6-trimethylphenyl)amine) (PTAA) was purchased from Xi'an Polymer Light Technology Corporation. Poly(3,4-ethylenedioxy-thiophene):poly(styrenesulfonate) (PEDOT:PSS) (Clevios P VP Al 4083) was purchased from H. C. Stark Company. CH3NH3I (MAI) and CH(NH2)2I (FAI) were purchased from Shanghai Materwin New Materials Co. Ltd. SnI2 (99.999%) was purchased from Alfa Aesar. PC61BM was purchased from American Dyes Source, Inc. ZnO nanoparticles were synthesized via a sol\\u2013gel process using Zn acetate and tetramethylammonium hydroxide ethanol (TMAH). TMAH\\u00b75H2O (543.24 mg) dissolved in ethanol (5.45 mL) was added dropwise to Zn(Ac)2\\u00b72H2O (657.33 mg) dissolved in DMSO solvent, followed by stirring for an hour at room temperature. After washing at least two times in ethanol, ZnO nanoparticles were dispersed in pure isopropanol at a concentration of \\u223c10 mg mL\\u22121. The ITO substrate was purchased from Hangzhou Hongshi Electronic Technology Co., Ltd, and its resistance is 8\\u201310 \\u03a9 per \\u03b3.\\n\\nThe one-step FA0.7MA0.3Sn0.3Pb0.7I3 precursor solution (1 M) was obtained via mixing stoichiometric amounts of FAPbI3 (1 M) and MASnI3 (1 M) precursors into a DMF and DMSO mixed solvent (molar ratio of 1:1) and stirring at 70 \\u00b0C for 2 h. The two-step Sn0.3Pb0.7I2 precursor solution (1 M) was prepared via dissolving SnI2 (111.75 mg) and PbI2 (322.70 mg) into 1 mL of DMF and 71 \\u03bcL of DMSO and stirring at 70 \\u00b0C for 2 h. The FA0.7MA0.3I precursor solution (1 M) was prepared via dissolving FAI (39.39 mg) and MAI (15.61 mg) into 1 mL of isopropanol. PC61BM was dissolved in chlorobenzene at a concentration of 20 mg mL\\u22121. PTAA was dissolved in toluene at a concentration of 5 mg mL\\u22121.\\n\\nThe ITO-coated glass substrates were cleaned via sonication using detergent, deionized water, acetone, and isopropanol sequentially for 20 min each, followed by 20 min of ultraviolet ozone (UV-ozone) treatment. Then a layer of 30 nm thick PEDOT:PSS was spin-coated onto the cleaned ITO at 4000 rpm for 40 s, and baked in air at 140 \\u00b0C for 15 min. The substrates were transferred into a glovebox (the O2 and H2O concentrations were kept below 0.01 and 0.02 ppm). A layer of 10\\u201315 nm thick PTAA can be formed via spin-coating at 6000 rpm for 45 s in the glovebox. The one-step perovskite films were fabricated via spin-coating 30 \\u03bcL of precursor solution at 5000 rpm for 45 s and quickly dripping 150 \\u03bcL of chlorobenzene on this 6 s after the beginning. The films were placed on a hotplate at 120 \\u00b0C for 4 min. The two-step mixed precursor solution was spun on the PEDOT:PSS or PTAA layer at 3000 rpm for 30 s. Then, the mixed FAI and MAI solution was spun on the substrate at 3000 rpm for 30 s. Afterward, the obtained films were annealed at 130 \\u00b0C or 160 \\u00b0C for 10 min. A layer of 40 nm thick PC61BM was spin-coated at 2000 rpm for 30 s. A 40 nm thick hole-blocking layer was deposited via spin-coating ZnO nanoparticles at 4000 rpm for 30 s on top of the PC61BM layer. Subsequently, samples were loaded into a vacuum deposition chamber (background pressure \\u2248 5 \\u00d7 10\\u22124 Pa) to deposit a 100 nm thick Al cathode with a shadow mask, defining an active device area of 6.0 mm2.\\n\\nThe J\\u2013V characteristics were measured in a glovebox under 100 mW cm\\u22122 AM1.5G solar irradiation, and the steady-state photocurrents were measured at a bias voltage (0.58 V) near the maximum power point and at a stabilized power output for a period of 300 s. EQE spectra were measured using a Stanford Research System Model SR830 lock-in amplifier unit coupled with a monochromator and a 500 W xenon lamp, and a calibrated Si photodiode with a known spectral response was used as a reference. X-ray diffraction (XRD) patterns were recorded at a scan rate of 5 deg min\\u22121 using a Rigaku D\\\\/max-2550PC X-ray diffractometer with Cu K\\u03b1 radiation (1.5406 nm). The film morphologies were characterized using SEM (Quanta 400). UV-vis absorption spectra were obtained with a UV-vis spectrometer (Cary-5000). Steady-state PL spectra were obtained with an FLS920 fluorescence spectrometer at an excitation wavelength of 400 nm.\\n\\n\",\r\n    \"Patterned FTO glass with a sheet resistance of 15 \\u03a9 sq\\u22121 was purchased from Wuhan Geao (China). PEDOT:PSS with brand Clevious P VP AI 4083 was purchased from H. C. Stark. Methylamine solution (33 wt% in absolute ethanol), hydriodic acid (57 wt% in water) and isopropanol (99.8%, extra dry) were purchased from Acros Organics. N,N-Dimethylformamide (DMF) and lead(II) iodide (99.999%) were purchased from Alfa Aesar. PCBM was purchased from Solarmer Energy, Inc. All these commercially available materials were used as received without further purification.\\n\\nCH3NH3I was synthesized according to the previous literature with some modification. Typically, 34 mL of methylamine (33 wt% in absolute ethanol) and 38 mL of hydroiodic acid (57 wt% in water) were mixed in a 150 mL three-necked flask, and then stirred at 0 \\u00b0C for 2 h in an ice-water bath. After that, the mixtures were rotary evaporated at 50 \\u00b0C for 1 h to remove the solvent and white CH3NH3I precipitates were recovered. Finally, the product was washed with diethyl ether three times and dried at 60 \\u00b0C overnight in a vacuum oven.\\n\\nThe patterned FTO was sequentially ultrasonic cleaned twice with detergent, pure water, deionized water, acetone and isopropyl alcohol. The pre-cleaned substrate was ultraviolet ozone treated for 10 min. After that, the filtered PEDOT:PSS aqueous solution was spin-coated onto the pre-treated FTO-glass substrates at 3000 rpm for 35 s and then dried at 150 \\u00b0C for 15 min. A 350 mg mL\\u22121 PbI2 DMF solution was spin-coated on the FTO\\\\/PEDOT:PSS substrate and then annealed at 100 \\u00b0C for 10 min. The CH3NH3I thin layer was deposited by spin-coating 40 mg mL\\u22121 CH3NH3I isopropyl solution at 1000\\u20133000 rpm for 20 s and then annealed at 80 \\u00b0C for 5 min. The PbI2 film and CH3NH3I film were pressed together face to face with a 0.2, 0.4, and 0.6 mm hollow aluminum foil gasket between them, and the space is sufficient for the thickness increase of the PbI2 film when it grows into a CH3NH3PbI3 crystal. The whole sets were then annealed at 150 \\u00b0C in a vacuum oven under a pressure of \\u22120.1 MPa or non-vacuum oven, and the perovskite film was obtained on the PbI2 side. The process of simplified CSS to fabricate perovskite is shown in Fig. 1. After that, PCBM solution (30 mg mL\\u22121 in chlorobenzene) was spin-coated on the perovskite layer at 3000 rpm for 30 s. Finally, a 100 nm Al cathode was deposited through thermal evaporation under a pressure of 5 \\u00d7 10\\u22125 Pa.\\n\\nThe current density\\u2013voltage curves were measured under AM 1.5G illumination (100 mW cm\\u22122) using a solar simulator (SAN-EI, AAA grade) with a Keithley 2400 Source Meter under an N2 atmosphere. The light intensity was calibrated with a Si solar cell for 1 sun. The external quantum efficiency (EQE) was measured using QE-R systems (Enli Tech.). The light intensity at each wavelength was adjusted with a standard single-crystal Si photovoltaic cell.\\n\\nThe thickness of the films was recorded using a DektakXT profilometer (Bruker Nano, Inc.). The surface morphologies of the thin films were examined using an AC Mode III (Agilent5500) atomic force microscope (AFM) operated in the tapping mode under ambient atmosphere. The surface and cross-section morphologies of the thin films were further characterized using a Scanning Electron Microscope (SEM; HITACHI SU8010, Japan) operated at an accelerating voltage of 5.0 kV and 30 kV, respectively. The crystallinity of the perovskite films were measured using an X-ray diffractometer (Rigaku miniflex 600) in the 2\\u03b8 range of 5\\u201390\\u00b0 at a scanning rate of 5\\u00b0 min\\u22121. The optical absorption of the films was measured using a Shimadzu UV-2450 UV-visible spectrophotometer.\\n\\n\",\r\n    \"CH3NH3I was synthesized by a method reported in the literature. PbI2 (99.99%), poly(3,4-ethylenedioxythiophene)\\\\/poly(styrenesulfonate) (PEDOT:PSS), [6,6]-phenylC61-butyric acid methyl ester (PC61BM), and bathophenanthroline (Bphen) were purchased from Xi'an Polymer Light Technology Corp. N,N-dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), tetrahydrofuran (THF), chlorobenzene (CB), ethanol, and isopropanol were purchased from Sigma. Tetraphenyldibenzoperiflanthene (DBP) was bought from Taiwan Nichem Co., Ltd.\\n\\nThe DBP precursor solution was prepared by dissolving 10 mg DBP in 2 ml THF or CB. After filtration, it was diluted to 1, 2, 3, and 4 mg ml\\u22121, respectively. The perovskite precursor solution was prepared by dissolving 0.3482 g of MAI and 0.922 g PbI2 (MAI:PbI2 = 1.095:1) into 0.9 ml of DMF and 0.1 ml of DMSO mixed solvent. PCBM precursor solution was formulated to 20 mg ml\\u22121 in CB and the formula for the Bphen precursor solution was 0.7 mg ml\\u22121 in ethyl alcohol.\\nFirst, the patterned indium tin oxide (ITO) transparent conductive glass was ultrasonically and subsequently cleaned with deionized water, acetone, and isopropanol for 15 min, respectively. Then, the ITO glass was dried with nitrogen and placed in a plasma cleaner for 5 min before use. After that, 15 \\u03bcl of PEDOT:PSS was spin-coated on the cleaned ITO at 6000 rpm for 30 s. Then, the films were annealed at 120 \\u00b0C on a hotplate for 15 min in the air. Subsequently, the sample was sent to the glovebox and the perovskite precursor solution was spin-coated on the PEDOT:PSS\\\\/ITO substrate at 6000 rpm for 30 s. During the spin-coating process, sec-butanol (250 \\u03bcl) as an anti-solvent was dropped on the wet CH3NH3PbI3 precursor film at the 8\\u201310th s after spin-coating started. Then, the resulting film was annealed at 100 \\u00b0C for 30 s. The above spin-coating process was carried out in a glovebox under a nitrogen atmosphere with a real-time humidity of about 1 ppm. Finally, the perovskite film was transferred to a hot plate, first annealed in ambient air (at 100 \\u00b0C for 30 min, real-time humidity of 30\\u201350%), and then annealed in a DMSO atmosphere at the same temperature and time. For the DMSO atmosphere, 50 \\u03bcl of DMSO was dropped into a glass Petri dish, and then the sample was covered with a glass Petri dish. Subsequently, 25 \\u03bcl DBP precursor solution was spin-coated on the perovskite layer at 4000 rpm for 30 s and 25 \\u03bcl PC61BM precursor solution (20 mg ml\\u22121 in chlorobenzene) was spin-coated at 3000 rpm for 30 s. Then, the Bphen interfacial layer with a concentration of 0.7 mg ml\\u22121 in ethanol was spin-coated at 6000 rpm for 30 s without additional annealing. The device was completed by evaporating a 100 nm thick Ag film as an electrode. The active device area was set to 0.04 cm2 by the overlap region between the top Ag cathode and the bottom ITO anode.\\n\\nSEM images and XRD patterns of the films were obtained with a JSM-7100F from JEOL and a D\\\\/Max-B diffractometer from Rigaku, respectively. AFM and SKPM images were obtained using an atomic force microscope from a Park systems NX10 equipped with scanning Kelvin probe microscopy (SKPM). A solar simulator (ABET SUN3000) was used to provide simulated solar irradiation (AM 1.5G, 100 mW cm\\u22122). The J\\u2013V characteristics were measured using a Keithley 2400 source meter. The output of the light source was adjusted using a calibrated silicon photodiode (ABET technology). The J\\u2013V measured the curve by a forward scan from \\u22120.5 to 1.5 V and a reverse scan from 1.5 to \\u22120.5 V. EQE (Keithley 2400) was measured using a power source (ZOLIX CSC1011) with a monochromator and a source meter. The steady-state and the transient-state PL spectra were measured by a xenon lamp at 467 nm and a nanosecond-pulsed laser at 376.2 nm using a fluorescence spectrometer (FLS980, Edinburgh Instruments). The absorption spectra were recorded by a Shimadzu UV-2600. Contact angles were measured by XG-CAMA1.\\n\\n\",\r\n    \"PSCs were fabricated with a regular n-i-p planar structure of ITO\\\\/SnO2\\\\/CsPbI2Br\\\\/poly-triarylamine (PTAA)\\\\/MoO3\\\\/Al. ITO-coated glass substrates (CSG Holding Co., Ltd, 10 ohm sq\\u22121) were cleaned stepwise with detergent, acetone, isopropanol and ethanol by sonication for 15 min each. After drying under a N2 stream, the substrates were treated with ultraviolet-ozone (UVO) for 15 min to generate a hydrophilic surface. The SnO2 colloid precursor (Alfa Aesar, 15 wt% in a H2O colloidal dispersion) was first diluted to 2.5 wt% with deionized (DI) water. Then, the diluted colloidal solution was spin-coated onto ITO substrates at 4000 rpm for 30 s, followed by annealing at 150 \\u00b0C for 30 min in ambient air. To avoid oxygen and moisture, the substrates were transferred into a nitrogen-filled glove box (<0.1 ppm O2 and H2O) for the rest of the device fabrication.\\nThe CsPbI2Br precursor solution was prepared by dissolving 208 mg of CsI (Sigma-Aldrich, 99.9%), 184 mg of PbI2 (TCI, 98%) and 148 mg of PbBr2 (Sigma-Aldrich, 99.999%) in 1 mL of DMF (Sigma-Aldrich, anhydrous, 99.8%) and DMSO (Sigma-Aldrich, anhydrous, 99.9%) (4:1, volume\\\\/volume), with stirring at 90 \\u00b0C for 2 h. The precursor solution kept at RT, was spin-coated on the ITO\\\\/SnO2 substrates heated at a certain temperature on a hot plate mounted on the spin-coater (hot-casting process; a photograph of the spin-coater is presented in Fig. S1, ESI\\u2020) or at RT (conventional RT-casting process) at 2500 rpm for 30 s. Right after spin-coating, the as-cast precursor film was annealed at a selected temperature for 10 min. A PTAA (Xi'an Polymer Light Technology Corp.) solution of 15 mg mL\\u22121 in chlorobenzene (Sigma-Aldrich, anhydrous, 99.8%) was then spin-coated on the perovskite at 3000 rpm for 30 s. Finally, 5 nm MoO3 and 100 nm Al were sequentially deposited by thermal evaporation at a base pressure of 9.0 \\u00d7 10\\u22125 Pa. The deposition rate and film thickness were monitored with a quartz crystal sensor. A shadow mask was put on the sample to define an active area of 4 mm2 before the metal deposition.\\n\\nThe current density\\u2013voltage (J\\u2013V) characteristics were measured using a Keithley 2400 source meter unit under simulated Air Mass 1.5 Global (AM 1.5 G) solar illumination at an intensity of 100 mW cm\\u22122, which was calibrated using a reference silicon solar cell. The measurements were carried out with the PSCs inside the glove box (<0.1 ppm O2 and H2O). The external quantum efficiency (EQE) spectra were measured using a QTEST HIFINITY 5 (Crowntech Inc., USA) at RT in air. The light intensity was calibrated using a single-crystal Si photovoltaic cell as a standard. X-ray diffraction (XRD) patterns were measured on a Rigaku-D\\\\/Max-3A X-ray diffractometer with monochromatic Cu K\\u03b1 irradiation (\\u03bb = 1.5406 \\u00c5). Scanning electron microscopy (SEM) analysis was performed on a Hitachi S-4800 electron microscope. Absorption spectra were acquired using a Shimadzu UV-2600 UV-vis spectrophotometer. Steady-state photoluminescence (PL) spectra were recorded on a Hitachi F-4600 fluorescence spectrophotometer.\\n\\n\",\r\n    \"The MASnxPb(1\\u2212x)I3 (MA = CH3NH3) perovskite precursor solution was formulated by dissolving a mixture of SnI2 (99.999%, Alfa Asear), PbI2 (99.999%, Alfa Aesar) and CH3NH3I (MAI, 99%, Xi'an Polymer Light Technology Corp.) in a molar ratio of x:(1 \\u2212 x):1.1 in a mixed solvent prepared using DMF (N,N-dimethylformamide, 99.5%, Aladdin) and DMSO (99.5%, Aladdin) at a volume ratio of 10:1. The MASnxPb(1\\u2212x)I3 thin films on the surface of the poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) substrate were formed by spin-coating the precursor solution at 6300 rpm, and after 5\\u201313 s of delay time the rotated wet films were washed with sec-butyl alcohol (99%, Aladdin) to promote fast nucleation and crystal growth. After the rotation stopped, the films were transferred onto a hot plate for annealing at 100 \\u00b0C for 25 s, followed by soaking in sec-butyl alcohol for 8\\u201310 s to remove excess MAI. Subsequently, the films were dried by spinning the substrates at 6300 rpm for 35 s. Finally, the films were thermally annealed at 100 \\u00b0C for 35 min under a N2 atmosphere and subsequently solvent annealed in a DMF atmosphere at 100 \\u00b0C for 35 min to assist the growth of crystalline domains. The film processes were conducted in a nitrogen-purged glove box with oxygen and moisture levels below 0.1 ppm. A schematic illustration of the fabrication steps of MASnxPb(1\\u2212x)I3 perovskite films is described in Fig. S1 in the ESI.\\u2020\\n\\nPerovskite solar cells have the structure of ITO\\\\/PEDOT:PSS\\\\/MASnxPb(1\\u2212x)I3\\\\/PC60BM\\\\/Al. Prior to the cell fabrication, the pre-patterned ITO-coated glass substrates were cleaned by ultrasonication sequentially with deionized water, acetone, and isopropanol for 20 min each. Next, the aqueous solution of PEDOT:PSS with a concentration of 1 mg ml\\u22121 (Heraeus) was spun onto ITO as a hole transport layer at 3000 rpm for 35 s in air, followed by annealing at 120 \\u00b0C for 10 min. Sequentially, MASnxPb(1\\u2212x)I3 perovskite films with a thickness of about 300 nm as an absorber were formed on the ITO\\\\/PEDOT:PSS substrate. Then, a chlorobenzene solution of [6,6]-phenyl-C60-butyric acid methyl ester (PC60BM, 99.5%, Solenne), with a concentration of 20 mg ml\\u22121, was spin-coated on top of the perovskite layer as an electron-transporting layer at 2000 rpm for 30 s. Finally, the device was obtained by thermal evaporation of an Al (150 nm) electrode.\\n\\nThe surface morphology of the films was analyzed using scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDS). The crystallinity of the perovskite films was examined by X-ray diffraction (XRD) measurements using a Rigaku D\\\\/Max-B X-ray diffractometer. The ultraviolet-visible (UV-vis) absorption spectra of the films were measured using an UV-Visible spectrometer with an integrating sphere (Shimadzu UV-2600). Current density\\u2013voltage (J\\u2013V) characteristics of all cells in the dark and under AM 1.5G illumination were measured using a programmable SourceMeter (Keithley 2400), with forward and backward scan rates of 0.08 V s\\u22121. The illumination was provided by a Sun 3000 Solar Simulator from ABET Technologies. The illumination power was corrected to 100 mW cm\\u22122 using a standard Si solar cell (certified by NREL). For the J\\u2013V measurement, a black mask with an aperture (0.16 cm2) was used to define the active area of the devices. The external quantum efficiency (EQE) as a function of wavelength was recorded using ZOLIX CSC1011 with a short arc xenon lamp source (Ushio UXL-553). The spot area of the incident beam is about 0.07 cm2. A Si photodetector model (certified by National Institute of Metrology, China) with known EQE was used to determine the spectral response of PSCs. All measurements were performed without encapsulation.\\n\\n\",\r\n    \"Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, Clevios P VP AI 4083) was provided by Heraeus. Copper(I) iodide (CuI, 99.999% trace metals basis), anhydrous acetonitrile (99.8%), anhydrous N,N-dimethylformamide (DMF, 99.8%), anhydrous 2-propanol (IPA, 99.5%), anhydrous chlorobenzene (CB, 99.8%), and anhydrous dimethyl sulfoxide (DMSO, 99.9%) were purchased from Sigma-Aldrich. Lead(II) iodide (PbI2, 99.9985%), methylammonium iodide (CH3NH3I; MAI), and formamidinium iodide (CH(NH2)2I; FAI) were purchased from Alfa Aesar and GreatCell Solar. [6,6]-Phenyl-C61-butyric acid methyl ester (PCBM) was purchased from Nano-C. Colloidal suspension of ZnO nanoparticles (Avantama N-10) was obtained from Avantama. All materials are commercially available and were used as received without further purification.\\n\\nThe p-i-n perovskite solar cells were fabricated with different combinations of ITO\\\\/hole transport layer (HTL): ITO\\\\/CuI, ITO\\\\/CuI\\\\/PEDOT:PSS and ITO\\\\/PEDOT:PSS\\\\/CuI. The device structure was ITO\\\\/HTL\\\\/perovskite\\\\/PCBM\\\\/ZnO NP\\\\/Ag. ITO-coated glass substrates were cleaned by sequential sonication in acetone and isopropyl alcohol (IPA) for 10 min each. N2 was blown to the glass\\\\/ITO substrates to complete the cleaning by removing IPA residues. Then oxygen plasma treatment was applied for 10 min. CuI solutions in acetonitrile with a concentration of 3 mg ml\\u22121 were prepared and stirred at room temperature for 3 h in a nitrogen filled glove box. CuI solutions were spin-coated on the cleaned ITO\\\\/glass substrates at 2000 rpm for 1 min. For some devices, CuI was spin-coated on top of PEDOT:PSS, or PEDOT:PSS was spin-coated on top of the CuI layer prior to the deposition of perovskites. As the surface of the CuI layer is hydrophobic, when PEDOT:PSS was spin-coated on top of CuI, a small amount of Dynol 604 (surfactant) was added to the PEDOT:PSS solutions to ensure good film coverage, and then the resulting solution was filtered through a 0.2 \\u03bcm PES filter. The filtered solutions were then spin-coated on the CuI-coated substrate at 3000 rpm for 1 min. All the following steps were performed in a glove box filled with nitrogen. PbI2 and MAI were dissolved (1.193 M for each) in a molar ratio of 1:1 in anhydrous DMF and the resultant mixture was stirred overnight at 70 \\u00b0C to produce the perovskite precursor solution. For the FAPbI3 precursor solution, FAI and PbI2 were dissolved (1 M for each) in a molar ratio of 1:1 in a mixed solvent with DMF and DMSO in a volume ratio of 4:1. The solutions were filtered with a 0.2 \\u03bcm PTFE filter before spin coating. The filtered perovskite precursor solutions were spin-coated at 5000 rpm for 55s on ITO\\\\/HTL substrates. During spin coating, 50 \\u03bcl anhydrous CB was dripped onto the substrate at 4\\u20135 s after spin coating started. After drying the perovskite films, MAPbI3 and FAPbI3 films were annealed on a hot plate at 100 \\u00b0C and 150 \\u00b0C for 20 min, respectively. Twenty milligrams of PCBM was dissolved in 1 ml anhydrous CB. To prepare the solution blends of PCBM and MAI, MAI was dissolved in anhydrous IPA at a concentration of 10 mg ml\\u22121. Then a small volume of the MAI solution was added into the PCBM solutions. Either PCBM solutions or PCBM:MAI solution blends were spin-coated at 2000 rpm for 1 min on top of the perovskite layer. Then, ZnO nanoparticles were spin-coated at 4000 rpm for 40 s. To complete device fabrication, Ag was thermally evaporated with a thickness of 100 nm in a vacuum chamber (\\u223c1 \\u00d7 10\\u22126Torr). The active area of the device is 5.25 mm2.\\n\\nThe current density\\u2013voltage (J\\u2013V) characteristics were recorded using a Keithely 2401 under 1 sun illumination (1000 Wm\\u22122 AM 1.5 G) from a solar simulator (Oriel Sol3A Class AAA Solar Simulators, Newport) using a xenon lamp. A standard silicon reference cell was used to calibrate the light intensity. Scans of J\\u2013V characteristics were performed with a forward (from short circuit to open circuit) and a reverse (from open circuit to short circuit) direction. The scan rate was 113 mV s\\u22121, unless indicated otherwise. To investigate the scan rate dependence, two different scan rates of 22.6 and 1130 mV s\\u22121 were considered. To age the devices, they were kept in the dark in the glove box before J\\u2013V characteristics measurements. The top view image of the CuI films prepared on ITO and PEDOT:PSS, and the cross-sectional image of the ITO\\\\/CuI\\\\/perovskite were acquired by scanning electron microscopy (SEM; JSM-7610F, JEOL) at an accelerating voltage of 5 kV. The optical absorption spectra of the perovskite films were collected with an Agilent 8453 UV\\u2013visible spectrophotometer. All the tested devices were unencapsulated.\\n\\n\",\r\n    \"Unless specified, all chemicals were purchased from Alfa Aesar or Sigma-Aldrich. Formamidinium iodide (FAI), methylammonium bromine (MABr), lead iodide (PbI2) and lead bromine (PbBr2) were purchased from Ying Kou You Xuan Trade Co., Ltd. Spiro-OMeTAD was purchased from Xi'an Polymer Light Technology Corp.\\n\\nReferring to the relevant literature, the FA0.85MA0.15Pb(I0.85Br0.15)3 mixed perovskite precursor solution was prepared by dissolving 1.4 M mixture of metal lead salts composed of 0.85 PbI2 and 0.15 PbBr2 and 1.3 M organic cations composed of 0.85 FAI and 0.15 MABr in anhydrous DMF:DMSO (4:1, volume ratio).\\n\\nThe etched FTO glass substrates were sequentially cleaned with detergent, deionized water, acetone, and 2-propanol in an ultrasonic bath for 10 min each. The glasses were then dried and treated by plasma for 5 min prior to use. An approximately 30 nm-thick TiO2 compact layer was sprayed on the hot FTO substrate using a 0.2 M titanium diisopropoxide-bis(acetylacetonate) solution and sintered at 450 \\u00b0C for 30 min. Afterward, according to our previous work, a mesoporous Na-treated TiO2 film was spin-coated at 5000 rpm for 50 s and then annealed at 500 \\u00b0C for 30 min. The perovskite layer was deposited via an anti-solvent method. Here, a 50 \\u03bcL perovskite precursor solution was spin-coated at 1000 rpm for 5 s and then at 4000 rpm for 60 s. During the second step, 120 \\u03bcL of chlorobenzene was dropped at the last 5th second. The substrates were then annealed at 120 \\u00b0C for 45 min. After cooling, the alternative hole transport layer (HTL) was deposited. According to a previous work, a Spiro-OMeTAD solution was prepared by dissolving 72.3 mg Spiro-OMeTAD powder in 1 ml chlorobenzene, to which 28.8 \\u03bcL 4-tert-butylpyridine and 17.5 \\u03bcL LiN(CF3SO2)2 (LITSFI) solutions (520 mg LiTSFI in 1 ml acetonitrile) were added. Thus, the 4-tert-butylpyridine and LiN(CF3SO2)2 (LITSFI) additives were added to the Spiro-OMeTAD solution. Then, the Spiro-OMeTAD solution was prepared according to a previous report and was deposited on the perovskite film at 3000 rpm for 30 s. The inorganic MnS HTL was prepared on top of the perovskite layer via thermal evaporation of MnS powder (Alfa Aesar, 99.9%) in vacuum of \\u223c1 \\u00d7 10\\u22124 torr using a thermal evaporator (Beijing Technol Science Co., Ltd). The evaporation rate was 0.9 \\u00c5 s\\u22121 and the Z-factor of MnS was 0.94. Finally, 80 nm gold was evaporated as the back electrode to form the entire device.\\n\\nThe crystal structures of MnS and perovskite films were characterized by an X-ray diffractometer (XRD-7000s, Shimadzu). The absorption and transmittance spectra of the films were measured by a UV-Vis spectrophotometer (Lambda 950, PerkinElmer). X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS) were performed using the XPS\\\\/UPS system (AXIS-ULTRA DLD-600 W, Shimadzu). The surface morphology and RMS roughness of perovskite and MnS thin films were characterized by atomic force microscopy (AFM, SPM9700, Shimadzu). The chemical composition and distribution of the constituents were observed by an electron probe microanalyzer (EPMA, EPMA-8050G, Shimadzu). The surface morphologies and microstructures of the perovskite and MnS films and the cross-sectional structure of perovskite solar cells were investigated by a field emission scanning electron microscope (FESEM, GeminiSEM300, Carl Zeiss) equipped with an energy-dispersive X-ray spectrometer (EDS). Fast component analysis of the MnS film was measured using an electron probe microanalyzer (EPMA-8050G, Shimadzu). The Ecopia HMS 5500 Hall system was applied to measure the room-temperature mobility and conductivity using the van der Pauw method with a magnetic field strength of 0.550 T. The photo-current density\\u2013voltage (J\\u2013V) characteristics were measured using a Keithley 2400 source meter under one-sun AM 1.5G (100 mW cm\\u22122) illumination with a solar light simulator (Model 71675-71580, Oriel Company). Photoluminescence (PL, excitation at 325 nm) and time-resolved photoluminescence (TRPL, excitation at 325 nm and emission at 760 m) spectra were obtained using a laser spectrometer (FLS 980, Edinburgh Instruments Ltd). The incident photon-to-electron conversion efficiency (IPCE) spectrum was measured using a Newport-74125 system (Newport Instrument). Electrochemical impedance spectroscopy (EIS, IviumStat 10800, Ivium Technologies) was performed under dark conditions and the frequency range was from 1 MHz to 100 MHz.\\n\\n\",\r\n    \"The perovskite photovoltaic devices had a structure of ITO\\\\/HTL\\\\/MAPbI3\\\\/[6,6]-phenyl-C61-butyric acid methyl ester (PC60BM)\\\\/C60\\\\/2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP)\\\\/Al. Indium tin oxide (ITO) coated glass substrates were cleaned successively with deionized water, acetone, and UVO cleaner (Jelight 42). HTL was either PEDOT:PSS or c-OTPD plus TPACA. PEDOT:PSS was spincoated onto ITO substrates at 3000 rpm for 50 s and dried in air at 135 \\u00b0C for 20 min. We deposited a 15 nm thick c-OTPD layer with 0.25 wt% TPACA 1,2-dichlorobenzene (DCB) solution onto an ITO substrate using spin-coating. Then, the c-OTPD film was cross-linked using a UV lamp and dried in N2 at 100 \\u00b0C for 10 min.\\nPerovskite and fullerene layers were deposited on top of the PEDOT:PSS or c-OTPD:TPACA layer inside a N2 atmosphere. In the doctor blade coating process, the precursor solution was dropped onto the HTL-covered ITO substrate, and swiped linearly by a glass blade at a high speed of 0.75 cm s\\u22121 (27 m h\\u22121). The substrates were held at elevated temperature during blade deposition (typically 125 \\u00b0C). The thickness of the perovskite films during blade coating was controlled by perovskite precursor solution concentration and the depth of the blading channel. Methylammonium iodide (CH3NH3I, MAI) and PbI2 dissolved in dimethylformamide (DMF) were used as the perovskite precursor solution. We primarily use 1:1 molar ratio between PbI2 and methylammonium halide, at a mass ratio of 40% PbI2 (400 mg per 1 mL DMF) and 13.8% methylammonium halide. We used 10\\u201320 \\u03bcL of precursor solution per 2.25 mm2 substrate. This was much lower than 50\\u2013100 \\u03bcL typically used for spin coating of similar perovskite solutions over the same area substrate, which demonstrated the advantages of high material usage by doctor-blade coating.\\nThe as-deposited perovskite films were subsequently thermally annealed at 100 \\u00b0C for 60 minutes while undergoing solvent annealing with 10 \\u03bcL of DMF according to our previously reported method. PC60BM, dissolved in 2% by weight DCB solution, was spin-coated on top of the perovskite layer at 6000 rpm for 35 s. The resulting film was further thermally annealed at 100 \\u00b0C for 60 minutes without solvent annealing. C60 (20 nm thick) and BCP (8 nm) were deposited by thermal evaporation. Finally, 100 nm Al was deposited with a mask to provide a cell area of 7.25 mm2 for majority of our devices.\\nWe used simulated AM 1.5G irradiation provided by a xenon lamp (Oriel 67005) to measure the photocurrent of our devices. The light intensity was calibrated using a Si diode (Hamamatsu S1133). The current\\u2013voltage (IV) relationship was measured using a source-meter (Keithley 2400), with our standard test procedure of scanning at 0.2 V s\\u22121. The external quantum efficiency (EQE) was obtained using a Newport QE measurement kit. Impedance spectroscopy measurements were made using a LCR meter (Agilent E4980A) under the simulated 1 sun irradiation. A Rigaku D\\\\/Max-B Diffractometer with Co K\\u03b1 was used to perform X-ray diffraction (XRD). Topographical and cross-section SEM (Quanta 200 FEG ESEM) imaging was performed after sputtering of Au onto samples (Cressington 108). The film thickness was measured by stylus profilometry (Bruker Dektak XTL).\\n\",\r\n    \"All materials were used as purchased without further purification unless specified otherwise. Organic solvents were purchased from Sigma Aldrich. Spiro-MeOTAD, CH3NH3I, and PbI2 were purchased from TCI.\\nPTZ-TPA was synthesized using a one-step Suzuki\\u2013Miyaura cross-coupling reaction. A mixture of 4-methoxy-N-(4-methoxyphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)aniline (0.560 g, 2.20 mmol), 3,7-dibromo-10-(4-octylphenyl)-10H-phenothiazine (0.545 g, 1.00 mmol), and Pd(PPh3)4 (0.028 g, 0.025 mmol) in toluene (10 mL) and a 2 M K2CO3 aqueous solution (5 mL) was stirred at 100 \\u00b0C for 24 h. After cooling down the reaction mixture to room temperature, the mixture was diluted with dichloromethane and washed with water. The organic layer was dried over Na2SO4 and the remaining solvent was evaporated. The crude product was purified by column chromatography (SiO2, petroleum ether\\\\/CH2Cl2 = 1\\\\/4 vol\\\\/vol) to obtain PTZ-TPA (0.789 g, 79.3% yield) as a yellow solid (1H NMR (500 MHz, CD2Cl2) \\u03b4 7.95\\u20136.10 (34H, m), 3.78 (12H, s), 2.73 (2H, s), 1.71 (2H, s), 1.30 (11H, s), 0.89 (3H, s); MS: m\\\\/z (M+) 992.544).\\nThe ultraviolet-visible (UV-vis) spectra of the solutions and of the solid thin films were obtained on a PerkinElmer Lambda750S spectrophotometer. Thermogravimetric analysis (TGA) was performed using a Discovery thermogravimetric analyzer. 1H NMR spectroscopy was performed using a Bruker DPX 400 MHz spectrometer. Matrix assisted laser desorption\\\\/ionization time-of-flight mass spectra were obtained on a Bruker Daltonics flexAnalysis. The highest occupied molecular orbital (HOMO) energy level of PTZ-TPA was measured using photoelectron yield spectroscopy under N2 (Model IPS-4). Steady-state photoluminescence spectra were measured using a FLS980 Spectrometer (Edinburgh Instruments). The samples were excited through the perovskite or PTZ-TPA layer with an excitation wavelength of 475 nm. Room-temperature photoluminescence (PL) decay curves were acquired for the perovskite films on fluorine doped tin oxide (FTO), for the perovskite films on PCBM\\\\/SnO2\\\\/FTO, of the Spiro-MeOTAD device, and of the PTZ-TPA\\\\/perovskite\\\\/PCBM\\\\/SnO2\\\\/FTO stack (excitation using a 405 nm-wavelength pulsed laser). The hole mobilities of PTZ-TPA and Spiro-MeOTAD were estimated using the space-charge limited current method with devices with a structure consisting of ITO\\\\/PEDOT:PSS\\\\/PTZ-TPA or Spiro-MeOTAD\\\\/Au. The current J\\u2013V curves of the devices were recorded using a Keithley 2400 source. Hole mobilities were calculated using the Mott\\u2013Gurney law by fitting eqn (1), where J is the current density, \\u03b50 is the permittivity of free space (8.85 \\u00d7 10\\u221212 F m\\u22121), \\u03b5 is the relative permittivity of the material (approaching 3 for organic semiconductors), \\u03bc is the hole mobility, V is the applied voltage, and d is the thickness of the active layer, respectively.\\n\\nPSCs were fabricated with the following structure: FTO\\\\/SnO2\\\\/PCBM\\\\/perovskite\\\\/PTZ-TPA\\\\/Au on patterned FTO glass. The FTO glass (with a sheet resistance of 20 \\u03a9 \\u25a1\\u22121, PV Tech, China) substrates were pre-cleaned using an ultrasonic bath of chlorobenzene and acetone followed by a treatment in an ultraviolet-ozone chamber (Novascan Company, USA) for 15 min. The SnO2 electron transport layer was applied following a previously reported procedure. SnCl2\\u00b72H2O in ethanol was used as a precursor solution (0.1 M). The precursor solution was spin-coated onto the substrate at a speed of 3000 rpm for 30 s and then the films were annealed under an ambient atmosphere at 180 \\u00b0C for 1 h. A thin layer of PCBM (10 nm) was prepared on the FTO\\\\/SnO2 surface at a speed of 2000 rpm and annealed at 100 \\u00b0C for 10 min. The PCBM solutions were prepared by dissolving 15 mg PCBM in 1 mL chlorobenzene. The perovskite (CH3NH3PbI3) layer (\\u223c320 nm) was then fabricated on the SnO2 film. The film was annealed at 90 \\u00b0C for 15 min. The hole-transporting materials PTZ-TPA (41 nm) were deposited by spin coating at 4000 rpm for 30 s from a chlorobenzene solution. The thickness of the photosensitive layer was measured using an Ambios Technology (USA) XP-2 profilometer. Finally, a 100 nm-thick Au film was deposited by thermal evaporation (Mbraun MB200) as the cathode. The active area (0.11 cm2) of the devices was determined by the overlap of FTO and the gold electrode. The current density\\u2013voltage (J\\u2013V) characteristics of the devices were measured with a computer-controlled Keithley (Zolix ss150 Solar Simulator) 236 source meter. The light source was a xenon lamp coupled with an AM1.5 solar spectrum filter; the optical power at the sample was 100 mW cm\\u22122. The incident photon-to-current conversion efficiency (IPCE) spectra were recorded using a solar cell quantum efficiency\\\\/external quantum efficiency measurement system (Zolix Solar cell scan 100) model SR830 DSP lock-in amplifier coupled with a WDG3 monochromator and a 500 W xenon lamp.\\n\\n\",\r\n    \"An aqueous dispersion of PEDOT:PSS (1.6 wt%, from H.C. Stark Baytron P, AI 4083) was obtained from Heraeus Co. Fullerene C60 was purchased from Solenne B. V., Netherlands. PbI2, PbBr2 (99.99%), CH(NH2)2CH3COO, HI(aq.), HBr(aq.) and BCP (2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline) were purchased from Aldrich Co. All materials were used as received except when specified. ITO-covered glass substrates were purchased from Ruilong Optoelectronic Co., Taiwan with photolithographic patterns designed by us. CH3NH3I, CH3NH3Br and CH(NH2)2I were synthesized from CH3NH2(aq.), CH(NH2)2CH3COO, HI(aq.) and HBr(aq.) with methods similar to those reported in the literature. GIXRD data were collected in the 2\\u03b8 range 5\\u00b0\\u201370\\u00b0 on a Bruker powder diffractometer (D8 Discover) using Cu K\\u03b11 radiation equipped with a 2D detector. The band gaps and Urbach energies of the perovskite films were obtained from their UV\\\\/Vis absorption spectra, which were recorded with a Hitachi U-4100 spectrometer. Scanning electron microscopy (SEM) images were taken with a Hitachi S-800 microscope at 10 kV. Samples for the SEM study were mounted on a metal stub with a piece of conducting tape and then coated with a thin layer of platinum film to avoid charging. The thickness of the films was measured from the cross-section SEM images. Nanosecond time-resolved photoluminescence (TR-PL) spectra were conducted using the time correlated single-photon counting (TCSPC) technique (UniRAM, Protrustech) along with the instrument response function of a 150 ps pulse duration and repetition rate of 20 MHz. The excitation wavelength was 405 nm. To prevent laser-induced thermal effects, the diameter of the spot size on the sample was increased to 50 \\u03bcm, and the excitation power was reduced to 0.1 mW. The spectra were taken with the perovskite film deposited on glass to eliminate the effects from the PEDOT:PSS hole transporter.\\n\\nThe MAPbI3 precursor solution (1.0 M) was prepared by adding equal moles of MAI and PbI2 to the anhydrous \\u03b3-butyrolactone (GBL)\\\\/dimethylsulfoxide mixture (DMSO) mixed solvent (volume ratio: 1:1). The MA1\\u2212xFAxPbI3 precursor solutions were made by replacing various amounts (0.1 mole, 0.2 mole, 0.3 mole and 0.4 mole, respectively) of MAI with FAI in the 1.0 M precursor solution. MA1\\u2212xFAxPbI3\\u2212yBry precursor solutions (without PbBr2) were formed when various amounts (0.15 mole, 0.3 mole and 0.45 mole, respectively) of MAI were replaced with MABr. The concentration (1.0 M) of all precursor solutions was the same. The precursor solutions composed of PbI2, PbBr2, MAI and FAI (as used by Jenet al.) in the GBL\\\\/DMSO (v\\\\/v: 1\\\\/1) mixed solvent with the exact same atomic stoichiometries as those using MAI, FAI, MABr and PbI2 as the starting materials were also prepared to study the effect of the starting materials on the photovoltaic performance of the resulting spin-coated films.\\n\\nPEDOT:PSS was spin-coated on top of cleaned, preheated ITO\\\\/glass at 5000 rpm for 30 s to form a hole-transporting layer (HTL) from its aqueous solution (1.6 wt%, AI 4083). After thermal annealing at 140 \\u00b0C for 10 min in air, in a glove box, the perovskite layer was deposited on top of the PEDOT:PSS film using one-step spin-coating combined with the anti-solvent washing method (1000 rpm for 10 s, 5000 rpm for 15 s, and in the last 5 s, toluene (100 \\u03bcl) was dropped on the film) to form a densely packed, fully-covered perovskite film. The perovskite film was thermal annealed (two-step) at 60 \\u00b0C for 30 s, 100 \\u00b0C for 30 s, and then 50 nm C60, 5 nm BCP and 100 nm Ag films were sequentially deposited on the perovskite to be the electron transporting layer (ETL), buffer layer and cathode electrode, respectively, using a high-vacuum thermal evaporator. The cells have an architecture of Glass\\\\/ITO\\\\/PEDOT:PSS\\\\/MA1\\u2212xFAxPbI3\\u2212yBry\\\\/C60\\\\/BCP\\\\/Ag with an active area of 0.2 cm \\u00d7 0.5 cm. The current density\\u2013voltage (J\\u2013V) curves were recorded using a Keithley 2400 source-measurement unit under a simulated AM 1.5G sun light at an intensity of 100 mW cm\\u22122 with a mask on the cell. The intensity of the simulated sunlight was calibrated using an NREL-certified Si solar cell (Oriel, 91150 V) with a KG-5 band pass color filter. The external quantum efficiency (EQE) or incident photo-to-current conversion efficiency (IPCE) was measured in air after sealing the device with a silica sealant and measuring immediately. A chopper and lock-in amplifier were used for the phase sensitive detection with the QE-R3011 measurement system (Enlitech Inc., Taiwan). The determination of the photovoltaic parameters and calibration of all the measuring facilities were the same as that reported previously.\\n\\n\",\r\n    \"Cesium carbonate, lead iodide, diphenylphosphinic acid (DPPA), oleylamine (OLA), oleic acid (OA), benzyl ether (BE), octadecene (ODE), toluene, ethanol, nickel oxide nanopowder, dimethylformamide (DMF), hydrochloric acid, zinc powder from Sigma Aldrich and TiO2 paste from Solaronix were of analytical grade and used as purchased.\\n\\nThe typical synthesis was done by placing 0.2 mmol PbI2 in 5 mL ODE, 0.5 mL OA and 0.5 mL OLA stirred in a 25 mL 3-necked flask. The flask content was degassed at 80 \\u00b0C for 30 min. Under a nitrogen flow, the temperature was raised to 150 \\u00b0C where 0.5 mL of Cs-OA (0.42 g Cs2CO3 dissolved in 8 mL at 150 \\u00b0C) was swiftly injected. After 10 s, the flask was quickly cooled down to room temperature in a cold water bath. The nanocrystals (NCs) were directly washed via centrifugation at 4500 rpm for 10 minutes followed by redispersion in toluene.\\n\\n2.3.1. OLA\\u2013OA addition by hot injection. Modification of OLA\\u2013OA addition was done using the same template as per the conventional approach. OLA and OA were added after drying PbI2 in ODE at 120 \\u00b0C for 1 hour. After all the PbI3 had dissolved under a nitrogen flow, the temperature was raised to 150 \\u00b0C. Cs-oleate (0.5 mL) as prepared above was quickly injected and the remaining steps followed those for conventional synthesis.\\n2.3.2. ODE and OA replacements. The solvents and ligands were changed from those used in conventional synthesis. ODE and OLA were replaced by toluene and benzene ether (BE) when the effect of other ligands such as DPPA was studied. Since DPPA is solid, the use of specific solvents capable of dissolving DPPA and the precursors is required. Nevertheless, the same protocol as that for the conventional approach was followed.\\n\\nFourier transform infrared (FTIR) spectroscopy was done using a Nicolet 1550 FT-IR spectrometer with a diamond crystal. UV-vis spectroscopy was done using a Cary 50, and the photoluminescence was studied on a Cary Eclipse with an excitation wavelength of 400 nm. The morphology of the synthesized nanoparticles was assessed using an FEI Tecnai T12 transmission electron microscope. The crystalline phase of the samples was determined using a PANalytical Empyrean X-ray diffractometer equipped with a Cu LFF HRDK40 X-ray tube.\\n\\nFTO-coated glass substrates were etched by sprinkling zinc powder on the surface followed by a few drops of HCl (2 M) to obtain the required electrode pattern. The substrates were sequentially sonicated in liquid detergent, distilled water, 2-propanol, acetone and ethanol for 10 min, respectively. Solaronix TiO2 paste was deposited onto the FTO coated substrate followed by sintering at 450 for 30 min. A CsPbI3 solution (5 mg mL\\u22121) was spin-coated on TiO2 at 1000 rpm for 30 s and then quickly baked at 100 \\u00b0C for about 1 min. This cycle was repeated until the active layer completely covered TiO2. The hole transporting layer was made by 3 cycles of spin-coating with NiO solution in dimethylformamide (0.5 M) onto the active layer at 1000 rpm for 15 s. Gold film was then deposited using a shadow mask via a sputter coater to a thickness of 50 nm. A device made of substrate-FTO-TiO2-CsPbI3\\\\/NiO-Au with a pattern area of 0.06 cm2 was fabricated. Contacts between FTO and gold were connected to the current\\u2013voltage measurement kit and the current characteristics were collected using a solar simulator set at 100 mW cm\\u22122 and under standard AM 1.5 conditions.\\n\\n\",\r\n    \"Methylammonium iodide (MAI) was provided by the Functional Phosphor Bank at Pukyong National University. If not stated otherwise, all chemicals were purchased from Aldrich. A 1.2 M perovskite precursor solution was prepared by dissolving equimolar PbI2 and MAI in a mixture of dimethyl sulfoxide (DMSO, 99.9%) and N,N-dimethylformamide (DMF, 99.8%) with the volume ratio as 1:9. The solution was stirred at 70 \\u00b0C overnight and filtered using 0.45 \\u03bcm nylon filters before use.\\n\\nThe solar cells were fabricated using the configuration of glass\\\\/indium tin oxide (ITO)\\\\/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)\\\\/MAPbI3\\\\/phenyl-C61-butyric acid methyl ester (PC61BM)\\\\/Al. The glass\\\\/ITO substrates were cleaned with water, ethanol and acetone in an ultrasonic bath for 15 min in sequence, and subsequently treated in a UV-ozone cleaner for 15 min. A PEDOT:PSS (Baytron PVP Al 4083) layer of 50 nm thickness was fabricated by firstly spin coating PEDOT:PSS onto the substrates at 4500 rpm for 40 s and then annealing it at 150 \\u00b0C for 20 min. Then, the substrates were transferred into a N2-filled glovebox. The perovskite precursor solution was spin-coated onto the ITO\\\\/PEDOT:PSS layer at 5000 rpm for 10 s. Antisolvent treatment was performed according to our reported study. Then, the two as-cast precursor films were placed together face to face, and then annealed at 100 \\u00b0C for 10 min, meanwhile preheat balance weight for applied pressure was put on the top substrate. To apply different pressures, we simply used different balances with different weights on the top substrate. After growth completes, the substrates with perovskite films were physically separated for further use. For comparison, the as-cast precursor film was directly placed on a hot plate at 100 \\u00b0C for 10 min, which afforded the reference film. Finally, PC61BM (20 mg mL\\u22121 in chlorobenzene) was deposited by spin coating at 1500 rpm for 30 s, forming an 80 nm transporting layer. Al electrodes with a thickness of 100 nm were finally evaporated under high vacuum (<2 \\u00d7 10\\u22126 Torr) through a shadow mask. The device area is defined as 0.04 cm2.\\n\\nX-ray diffraction (XRD) experiments were performed by using a Philips X-ray diffractometer with Cu K\\u03b1 radiation. The surface morphologies of the perovskite films were obtained by SEM (S-2700, Hitachi, Japan). The UV-Vis absorption spectra of the perovskite films were collected on a Varian 5E UV\\\\/vis\\\\/NIR spectrophotometer. Photocurrent density\\u2013voltage (J\\u2013V) curves were obtained under AM 1.5 G irradiation (100 mW cm\\u22122) with a solar simulator and a Keithley 2400 source meter. The light intensity was adjusted using a calibrated Si solar cell. External quantum efficiency (EQE) was measured in direct current (dc) mode, where a xenon lamp was used as a light source for generating a monochromatic beam.\\n\\n\",\r\n    \"PEDOT:PSS was obtained from Heraeus (Clevios P VP. Al 4083). The lead iodide (PbI2, beads, 99.999% trace metals basis) was purchased from Sigma Aldrich and methylammonium iodide (MAI, MS101000-10) was purchased from Dyesol Pty Ltd. All commercial products were used as received.\\n\\nThe small area (0.2 cm2) devices were fabricated on glass substrates (2.5 cm \\u00d7 2.5 cm) with a pre-patterned ITO layer (Xinyan, \\u223c18 \\u03a9 sq\\u22121). The electrodes were cleaned using Alconox (detergent) solution and a soft cloth before being sonicated in sequence with Alconox, de-ionized water, acetone and 2-propanol for 10 min each, and then dried under a nitrogen flow. For the large area devices 6 cm \\u00d7 6 cm glass substrates with an ITO layer (Kintec, \\u223c13 \\u03a9 sq\\u22121) were patterned by photolithography and etched with 5 M hydrochloric acid. The electrodes were cleaned using Alconox solution and a soft cloth before being sonicated in sequence with Alconox, de-ionized water, acetone and 2-propanol for 10 min each, and then dried under a nitrogen flow. For the large area devices with metal grids, 750 nm thick silver, gold or aluminum lines (width 550 \\u00b1 50 \\u03bcm, with the pitch between the lines being dependent on the number of lines) were thermally evaporated through a shadow mask at a vacuum of 10\\u22126 mbar. The substrates with the aluminum grid were then exposed to a UV-ozone plasma (MBraun, MB UV-O3) for 15 min to grow the oxide layer. Each of the substrates were coated with a 30 \\u00b1 5 nm PEDOT:PSS layer by spin-coating at 5000 rpm for 30 s before being dried on a hot plate at 170 \\u00b0C for 10 min. All the substrates were then transferred into a nitrogen filled glove box for device fabrication (O2 < 5 ppm, H2O < 5 ppm). CH3NH3PbI3 thin films were spin-coated as per the method reported by Jeon et al. 1.2 M PbI2 and MAI (e.g., 553 mg PbI2 and 191 mg MAI in 1 mL of solvent) were dissolved in a mixed solvent of \\u03b3-butyrolactone (GBL) and dimethyl sulfoxide (DMSO) (7:3 v\\\\/v) with stirring and heating at 60 \\u00b0C for 2 h. The solution was then dispensed onto the substrate until it was fully covered and spin-coated at 3000 rpm. After 42 s 1.7 mL of toluene was dispensed onto the middle of the spinning organohalide perovskite film. After a further 38 s of spinning at 3000 rpm the spin speed was increased to 5000 rpm for 20 s to dry the film. The substrates were then further dried on a hot plate at 100 \\u00b0C to fully convert the film to the organohalide perovskite. In the next step a 10 mg mL\\u22121 PC60BM in toluene solution was spin-coated onto the CH3NH3PbI3 layer at a spin speed of 1000 rpm for 20 s. The devices were heated on a hot plate at 70 \\u00b0C for 10 min. Finally, 1 nm of LiF and 200 nm of Ag were deposited by thermal evaporation under a 10\\u22126 mbar vacuum with a shadow mask to complete the device.\\n\\nThe morphology of the organohalide perovskite films and the cross-sectional structure of the solar cells were measured using a Hitachi SU3500 scanning electron microscopy (SEM) and a Jeol JSM-7100F field-emission scanning electron microscopy (FESEM) (Jeol JSM-7100F). The X-ray photoelectron spectroscopy (XPS) data were collected on a Kratos AXIS Ultra with a monochromatic Al X-ray source at 150 W and analyzed with CasaXPS software. The water contact angle of the grid lines were measured by a PSS OCA20 optical contact-measuring system. For the thickness mapping a SCI FilmTek 2000M spectroscopic reflectometer was used.\\n\\nCurrent density\\u2013voltage (JV) characteristics were acquired in a nitrogen filled glovebox (O2 < 1 ppm, H2O < 1 ppm) using a Keithley 2400 Source Measure Unit and Agilent B1500A semiconductor analyzer. The simulated Air Mass 1.5 Global (AM 1.5 G) illumination was provided by an Abet Sun 2000 Solar Simulator. The light intensity used throughout was \\u223c1000 W m\\u22122 (the exact number being used for efficiency calculations) as determined by an NREL-calibrated silicon reference cell with a KG5 filter. For the large area devices (25 cm2) the JV curves were measured using an Agilent B1500A semiconductor analyzer with a 4-wire configuration to eliminate the effect of the cable resistances and SMU internal impedance in the measurement circuit. The reason for this is that for the large area devices the current flowing in the circuit was much higher than for the small area devices resulting in a larger voltage drop over the cable resistance and SMU impedance, and thus the four-wire configuration compensates for the voltage drop. For the 0.2 cm2 devices 10 samples and for the 25 cm2 devices three samples were fabricated and tested. EQEs were measured with a QEX7 setup from PV Measurements Inc., using a calibrated photodiode. The area of the focused beam was approximately 0.15 cm2. The white light short circuit current and integrated small perturbation EQE currents were determined to be within 10% of each other as a final validation of the measurement protocols.\\n\\n\",\r\n    \"2.1.1. Materials. An aqueous dispersion of PEDOT:PSS (AI 4083) was obtained from Heraeus Co. Fullerene derivatives (PC61BM (99.8%)) were purchased from Nano-C Co. TOPD, bis(2,4-pentanedionato)molybdenum(VI) dioxide (MoO2(acac)2) and PbI2 (99.999%) were purchased from Alfa Aesar. All these commercially available materials were used as received without further purification.\\n2.1.2. Synthesis of CH3NH3I. CH3NH3I was synthesized through the reaction of 28.7 mL methylamine (40 wt% in methanol, Aladdin) and 29.8 mL hydroiodic acid (57 wt% in water, Aladdin) under nitrogen atmosphere in 250 mL round-bottom flask in an ice bath for 2 h with stirring. The crystals of methylammonium iodide (CH3NH3I) were collected using a rotary evaporator at 50 \\u00b0C for 2 h to remove the solvent. The product was dissolved in ethanol, followed by re-crystallization by diethyl ether. The crystals were filtered and washed three times with diethyl ether. At last, the solid was dried at 60 \\u00b0C in vacuum oven overnight. The detailed process is shown in .\\n\\nITO glasses (AGC, 11-8, 7 \\u03a9 sq\\u22121) were patterned by laser cutting and ultrasonically cleaned with detergent, deionized water, acetone and isopropanol for 20 min, sequentially, followed by plasma cleaning for 20 min prior to use. 5 mg mL\\u22121 of MoO2(acac)2 isopropanol solution was spin-coated at 4000 rpm for 30 s on the precleaned ITO glass, and then baked in air at 150 \\u00b0C for 10 min to prepared s-MoOx film, followed by plasma cleaning for 1 min. Subsequently, PEDOT:PSS aqueous solution filtered through a 0.22 \\u03bcm filter was spin-coated at 4000 rpm for 30 s on the s-MoOx film, and then baked at 120 \\u00b0C in air for 15 min. Then the ITO\\\\/s-MoOx\\\\/PEDOT:PSS substrate was transferred to a nitrogen-filled glove-box for the perovskite film deposition. 461 mg of PbI2, 159 mg of CH3NH3I was dissolved in a mixed solvent of DMF and DMSO (7:3, v\\\\/v) at 60 \\u00b0C with stirring for 12 h to prepare perovskite precursor. 40 \\u03bcL completely dissolved perovskite precursor solution was spin-coated on the PEDOT:PSS layer at 500 rpm for 3 s, followed by 4000 rpm for 30 s. 240 \\u03bcL of chlorobenzene was quickly dripped on the rotating substrate at the beginning of 8\\u201312 s in the second spin coating step. The substrate was immediately dried on a hot plate at 100 \\u00b0C for 10 min and obtained a dense CH3NH3PbI3 film. After that, 20 mg mL\\u22121 of PCBM solution in chlorobenzene was spin-coated at 1000 rpm for 20 s on the perovskite absorber layer. The TOPD buffer layer was prepared by spin-coating a 3 mg mL\\u22121 TOPD isopropanol solution on the PCBM at 4000 rpm for 30 s and then stays in glove box for 24 hours for solvent annealing. The thickness of the TOPD layer was about 10 nm. Finally, Ag electrode was deposited by using thermal evaporator at a constant evaporation rate of 1 \\u00c5 s\\u22121.\\n\\nScanning electron microscope (SEM) images were obtained by using FE-SEM (ZEISSUltra55). Transmittance spectra were recorded with an integrating sphere system (Ocean Optics, USA) in the 400\\u2013900 nm range. X-ray diffraction (XRD) analysis was performed on a PANalytical X'Pert PRO diffractometer with the Cu-K radiation at a scan rate of 4\\u00b0 min\\u22121. Steady-state PL spectra were measured using an excitation wavelength of 467 nm in an HORIBAfluorolog3. TRPL measured by Time Correlated Single Photon Counting (TCSPC, picoharp300) with a femto second laser source. J\\u2013V curves measurements were carried out using Keithley 2400 at room temperature under AM1.5G illuminations (1000 W m\\u22122) from a solar simulator (Newport, 91160), which was calibrated using a standard silicon solar cell device by the NREL. The incident photon to converted current efficiency (IPCE) spectra was measured from 300\\u2013850 nm using a Xe source (Newport, 66902). The light intensity at each wavelength was calibrated with a standard single-crystal Si photovoltaic cell. The IPCE measurement was performed under ambient atmosphere at room temperature. EIS was measured with a CHI6601 Electrochemical Workstation with an AC signal of 200 mV in the frequency range of 0.1 Hz to 1 MHz.\\n\\n\",\r\n    \"Fluorine doped tin oxide (FTO) coated glasses (1.5 cm x 1.5 cm) were etched by using hydrochloric acid and zinc powder to obtain two separated the electrodes. The wet-etched FTO glasses were cleaned ultrasonically in detergent solution, acetone, isopropyl alcohol for 15 min sequentially and then rinsed with deionized water for 15 min. Clean substrates were dried with nitrogen gun and subsequently treated with oxygen plasma for 5 min to eliminate organic traces. Onto cleaned FTO glasses, thin c-TiO2 layer was spin coated by using solution of titanium (IV) isopropoxide (99.9%, Sigma-Aldrich, as received) and acetyl acetone (99.5%, Sigma-Aldrich) in absolute ethanol at 1500 rpm for 20 s, followed at 2000 rpm for 20 s. Before drying, the coated substrates were sintered 450\\u00b0 C for 30 min to form a compact n-type layer of TiO2 in air.\\nThe SAM modified substrate were fabricated by a simple method, which can be seen in Fig. 2 . Firstly, 1 mM of SAM solutions were prepared by solving 1-OMe, 2-OMe and 3-OMe in dimethyl sulfoxide (DMSO). c-TiO2 coated substrates were immersed in SAM solutions for overnight to perform covalently bonding. Then, substrates were removed from solutions and rinsed to eliminate physically absorbed molecules with DMSO, acetone and DMSO, respectively. The perovskite absorber layer and hole transport layer (HTL) was deposited under N2 atmosphere in glovebox onto SAM-modified and non-modified c-TiO2 coated FTO. MAPbI3 pre-mixed perovskite solution was prepared by mixing 1.54 mol of CH3NH3I (Dyesol) and 1.23 mol of PbI2 (99.999%, Alfa Aesar,) in 2.5 mL \\u0263-butyrolactone (GBL, anhydrous, 99.9%, Sigma Aldrich) and stirred at room temperature for overnight. 70 \\u03bcL perovskite solution was deposited by spin-coating at 4000 rpm for 50 s and 70 \\u03bcL toluene was dropped rapidly in one-shot at last 35 s of spinning substrate to obtain a uniform and flat intermediate-phase film. Then perovskite coated substrate were annealed at 85\\u00b0 C for 15 min. The dopant free hole transporter material P3HT solution was prepared by dissolving 20 mg of poly(3-hexylthiophene-2,5-diyl) in 1 mL of chlorobenzene and mixed at 70\\u00b0 C for overnight. Prepared solution was spin-coated at 1500 rpm for 15 s and at 2000 rpm for 15 s. Finally, 10 nm of MoO3 and 100 nm of Ag were thermally evaporated on top of the HTM layer, respectively.\\n\\nThe structural and morphological analyses of as-prepared films were carried out by contact angle goniometer (Kruss Easy Drop), X-ray diffraction (XRD, Bruker D8 Advance), scanning electron microscope (SEM, Zeiss Evo). The optical properties were characterized by ultraviolet-visible (UV\\u2013vis) absorption spectroscopy (Biochrom Libra S22 spectrometer). The X-ray Photoelectron Spectroscopy (XPS) results were recorded by SPECS EA 300 equipped with Al monochromatic anode. Atomic force microscope (AFM) analyses were performed by using NT-MDT AFM NTEGRA Solaris in \\u201ctapping\\u201d mode and work function measurements of SAM modified and non-modified substrates were carried out in Kelvin Probe mode. Bruker DektakXT surface profilometer was used to measure thin film thicknesses. The photovoltaic J\\u2013V characteristics of as-fabricated perovskite solar cells without any encapsulation were tested under N2 ambient in glovebox using Keithley 2400 source meter. AM1.5 light source (Atlas) was used as solar simulator. The external quantum efficiencies were recorded as a function of wavelength from 350 nm to 800 nm under N2 by using a monochromatic light from Xenon-lamp connected to EG&G 7260 DSP Lock-in amplifier to measure the photocurrent response.\\n\\n\",\r\n    \"CH3NH3I (Dyesoltimo), PbI2 (99.99%, TCI Co., Ltd.), \\u03b3- butyrolactone (GBL, Sigma Aldrich), and dimethyl sulfoxide (DMSO, Junsei) were used to generate the CH3NH3PbI3 (MAPbI3) solution. The hole transport layer of PEDOT:PSS (AI4083 was supplied by the ECS group) and the electron transport layer of 6,6-phenyl-C71 butyric acid methyl ester (PC71BM)\\\\/TiOx (precursor: Titanium(VI) isopropoxide, Sigma Aldrich) were used for an efficient structure. 1-hydroxycyclohexyl phenyl ketone (HCPK, Aldrich) and aliphatic urethane diacrylate oligomer (EB 9270, ENTIS), and perfluoropolyether (PFPE, Aldrich) were used for the synthesis of the modified (hydrophobic) polyurethane acrylate (PUA) mold films. The modified PUA film of relatively hydrophobic property was fabricated using a method reported previously [33].\\n\\nITO glass substrates were cleaned using dishwasher detergent, and ultrasonicated under deionized water, acetone, and isopropanol sequentially for 20\\u202fmin each. To compare between transfer printing and spin-coating, the PEDOT:PSS was diluted in methanol at a 1:1\\u202fvol ratio, and coated onto the UVO-treated PFPE-PUA and ITO, respectively, at 3500\\u202frpm for 60\\u202fs with a thickness of 30\\u202fnm. Subsequently, the PEDOT:PSS layer was transferred from PFPE-PUA to the ITO surface under 95\\u202f\\u00b0C and uniform pressure. The PEDOT:PSS-deposited substrates were annealed on a hot plate at 140\\u202f\\u00b0C for 10\\u202fmin, to form a thin film with a thickness of 30\\u202fnm. The MAPbI3 solution was composed of CH3NH3I and PbI2 (1.06:1 mol.%) in GBL and DMSO (7:3\\u202fvol ratio), with a molar concentration of 1.4\\u202fmol\\\\/L at room temperature for 12\\u202fh. To generate the perovskite film, a solution of MAPbI3 was spun on the PEDOT:PSS film at 1000\\u202frpm for 30\\u202fs, and subsequently 5000\\u202frpm for 30\\u202fs with the additional treatment of toluene. Following that, the substrates were placed on a hot plate at 100\\u202f\\u00b0C for 5\\u202fmin, to form the crystallized MAPbI3 film with a thickness of 300\\u202fnm. To fabricate PC71BM with a thickness of 30\\u202fnm, the PC71BM solution was dissolved in chlorobenzene with a concentration of 20\\u202fmg\\\\/mL, and spin-coated onto the surface of MAPbI3 at 2000\\u202frpm for 40\\u202fs. Subsequently, the TiOx layer with a thickness of \\u223c10\\u202fnm was formed at 5000\\u202frpm for 40\\u202fs, using a molar concentration of 25\\u202fmmol\\\\/L. Finally, an Al cathode was deposited thermally under 1.9\\u202f\\u00d7\\u202f10\\u22126\\u202fTorr with a thickness of 100\\u202fnm by thermal evaporation.\\n\\nThe surface morphology and roughness of several thin films were observed by atomic force microscope (AFM) in the noncontact mode (Park NX10), and field emission scanning electron microscopy (FE-SEM) (SIGMA model from Carl Zeiss, Inc.) at 5\\u202fkV. The contact angles of water droplets on the mold film and PEDOT:PSS thin film were measured using a contact angle analyzer (SEO, Phoenix 300 THOUCH). The electrical performances of the PSCs were measured under a solar simulator (Peccell Technologies, Inc., PEC-L01) with air mass 1.5 global (AM 1.5 G) at an intensity of 100\\u202fmW\\\\/cm2, which was calibrated by a silicon reference cell. The current-density\\u2013voltage characteristics of the PSCs were measured using an electrical measurement system (ZIVE SP1). The EQE was measured after power calibration (ABET Technologies, Inc., LS150) with a monochromator (Dongwoo Optron Co. Ltd., MonoRa-500i). The crystallinity of the perovskite thin film was analyzed by XRD spectra (Bruker-AXS, New D8-Advance). The X-ray photoelectron spectra (XPS) was recorded with a K-Alpha\\u202f+\\u202fspectrometer (ThermoFisher Scientific). The PL spectra were measured by Raman microscopy (Xperam200 (Nanobase Inc.)). The laser wavelength was 642\\u202fnm, and the power was 0.3 mW for each device. The magnification of the object lens was 40\\u00d7. We calculated the average of ten datasets of the Raman spectra in the same position for each sample.\\n\\n\",\r\n    \"Device Fabrication: The ITO-coated glass substrates (sheet resistance: 6.4\\u202f\\u03a9 sq\\u20131) were cleaned ultrasonically with abstergent aqueous solution, deionized water, acetone, and isopropyl alcohol for 20\\u202fmin, and then dried under a stream of N2. The substrates were then cleaned with air plasma for 10\\u202fmin. A NiOx film (ca. 20\\u202fnm) was prepared by spin-coating a solution containing the NiOx precursor [nickel(II) acetylacetonate (129\\u202fmg) dissolved in EtOH (5\\u202fmL) containing HCl (38\\u202fwt%, 50\\u202f\\u03bcL)]. The NiOx-coated substrates were then baked at various temperature for various periods (min) in air [44]. The MAPbI3 precursor solutions (with or without 3\\u202fwt% urea) were prepared by dissolving 1.2\\u202fM PbI2 and MAI (molar ratio, 1:1) in anhydrous DMF\\\\/DMSO (4:1). The solution was stirred at 60\\u202f\\u00b0C for 2\\u202fh in an Ar-filled glove box. The perovskite precursor solutions were spin-coated on the NiOx-coated substrates in two steps (step 1: 2000\\u202frpm for 10\\u202fs; step 2: 4000\\u202frpm for 20\\u202fs), and then toluene (100\\u202f\\u03bcL) was applied rapidly to the substrates to induce fast crystallization. Finally, the samples were annealed at 100\\u202f\\u00b0C for 10\\u202fmin to complete the transformation to the perovskite [53]. PC61BM (20\\u202fmg\\u202fmL\\u22121 in anhydrous chlorobenzene) was deposited; following the deposition of BCP (2\\u202fmg\\u202fmL\\u22121 in IPA), spin-coating was performed at 6000\\u202frpm for 30\\u202fs. Finally, the device was completed through the evaporation of Ag or Au contact electrodes (100\\u202fnm) at a vacuum level of 10\\u20137 Pa through a shadow mask. The active area of this electrode was fixed at 10\\u202fmm2.\\n\\nThe cell performance was measured inside a glove box. The current\\u2013voltage (I\\u2013V) properties of the devices were measured using a computer-controlled Keithley 2400 source measurement unit (SMU) and an Enlitech simulator (AAA Class Solar Simulators) under AM 1.5 illumination (1000\\u202fW\\u202fm\\u22122). The illumination intensity was calibrated using a standard Si reference cell and a KG-5 filter. EQEs were measured using an Enlitech QE-R spectral response measurement system to calibrate the current densities of the devices. The morphologies of the perovskites were analyzed through FE-SEM (JEOL JSM 6701F). Grazing-incidence wide-angle X-ray spectroscopy (GIWAXS) was performed using a Philips Panalytical-x\\u2019PertPROMRD instrument; the incident beam angle was above the critical angle (ca. 0.5\\u00b0). TRPL spectra were recorded using a time-correlated single photon counting spectrometer (WELLS-001 FX, DongWoo Optron). The pulse laser had a wavelength of 440\\u202fnm and an average power of 1 mW; it was operated with a duration of excitation of 2\\u202f\\u03bcs. XPS was performed using a ULVAC-PHI PHI 5000 Versaprobe II spectrometer and a monochromatic Al K\\u03b1 source. WFs were calculated using an incident light energy of 21.2\\u202feV [He(I) emission]. The samples were biased at \\u20135 V dc to drive low-energy secondary electrons into the detector.\\n\\n\",\r\n    \"Hydrochloric acid (HCl; 37% AR.), chlorobenzene (AR.) and N,N-Dimethylformamide (DMF; AR.) were obtained from RCI Labscan. Isopropanol (anhydrous, \\u226599.5%), lead (II) iodide (PbI2; 99%), were obtained from Sigma-Aldrich. PEDOT:PSS and PC60BM (PCBM; 99.0%) were obtained from Ossila. Methylammonium iodide (MAI; CH3NH3I) was obtained from Dyesol. All the materials were directly used without further purification.\\n\\nPerovskite solar cells based on p-i-n heterojunction structure of FTO\\\\/PEDOT:PSS\\\\/CH3NH3PbI3\\\\/PCBM\\\\/Ag were studied. FTO substrate was patterned by an equal volumetric mixtures of HCl:deionized (DI) water with Zn metal. The patterned FTO was cleaned under sonicator with detergent, DI water, acetone and isopropanol for 15\\u00a0min each, respectively, and dried with flowing N2. A hole transport materials (HTMs) was prepared from a mixtures of PEDOT:PSS and methanol with a volumetric ratio of 1:2, respectively. The mixed solution was sonicated for 30\\u00a0min in ambient condition. The PEDOT:PSS solution was spin-coated on the patterned FTO at 3000\\u00a0rpm for 60\\u00a0s. After the spin-coating, the PEDOT:PSS-coated FTO was annealed at 150\\u00a0\\u00b0C for 15\\u00a0min, cooling down to room temperature and transfer to a low relative humidity (<20%) grove box. CH3NH3PbI3 was formed using two-step spin-coating deposition process. For PbI2 layer deposition, PbI2 solution was prepared by dissolving 1\\u00a0M PbI2 in DMF. The solution was stirred at 70\\u00a0\\u00b0C. Before the deposition, the PEDOT:PSS films was pre-heated at 70\\u00a0\\u00b0C for 15\\u00a0min. Next, 120\\u00a0\\u03bcl of the PbI2 solution was spin-coated on the PEDOT:PSS films at 3000\\u00a0rpm for 30\\u00a0s, and immediately annealed at 70\\u00a0\\u00b0C for 15\\u00a0min. After cooling down, 120\\u00a0\\u03bcl of MAI solution was deposited on the PbI2 films with spin-coating rate of 2000\\u00a0rpm for 30\\u00a0s and annealed at 100\\u00a0\\u00b0C for 2\\u00a0h under flowing N2 gas to form CH3NH3PbI3 films. The MAI solution was prepared by dissolving 50\\u00a0mg\\\\/ml MAI in isopropanol and maintained by stirring at room temperature. For PCBM preparation, PCBM solution was prepared by dissolving PCBM in chlorobenzene with concentration of 20, 30, 40 and 50\\u00a0mg\\\\/ml. Two sets of PCBM solution was separated stirring at room temperature (non-heat) and 70\\u00a0\\u00b0C (pre-heat) for 12\\u00a0h. The non- and pre-heat PCBM solutions were deposited by spin-coating on the CH3NH3PbI3 films at 2000\\u00a0rpm for 30\\u00a0s. Finally, the Ag back contact was deposited on the PCBM layer by thermal evaporation.\\nMorphology of deposited films was observed by field emission scanning electron microscopy (FE-SEM, JEOL JSM-6335F) operating at a voltage of 15.0\\u00a0kV. Photovoltaic characteristics were measured under standard simulated solar radiation of 100\\u00a0mW\\\\/cm2 (AM1.5).\\n\\n\",\r\n    \"For polymerization, 0.2 M of pyrrole monomer (C4H5N, 0.67 ml, Sigma\\u2013Aldrich, \\u2a7e99.5%) was first dissolved in 50 ml of deionized (DI) water and was kept stirring for 30 min at the room temperature. Thereafter, the aqueous ammonium peroxysulphate ((NH4)2S2O8, 0.2 M, Sigma\\u2013Aldrich, \\u2a7e99.5%) was added drop wise to the reaction mixture, using peristaltic pump. After completion of the reaction, the obtained blue-green color precipitates were centrifuged at \\u223c4000 rpm for 10 min. The final product was washed with copious amount of DI water, methanol and dried in vacuum oven at \\u223c40 \\u00b0C for 24 h [17].\\n\\nMethylamine (27.86 ml, CH3NH2, 40% in methanol, TCI chemicals) and hydroiodic acid (30 ml of 57 wt% in water, HI, Aldrich, 99%) were used to synthesize methylammonium iodide (CH3NH3I), as reported elsewhere [18]. In brief, the reaction mixture of CH3NH2 and HI was placed in a chiller and maintained at 0 \\u00b0C for 4 h to obtain precipitates which were recovered by the evaporation at 50 \\u00b0C for 1 h. The final yellow product of CH3NH3I was repeatedly washed with diethyl ether ((C2H5)2O Alfa Aesar, 99% assay) and dried at 60 \\u00b0C in vacuum oven for 24 h. For the synthesis of CH3NH3PbI3, an equimolar CH3NH3I, and lead iodide (PbI2, Aldrich, 99%) were dissolved in \\u03b3-butyrolactone (C4H6O2, TCI, 99%), and kept at 60 \\u00b0C for 12 h.\\n\\nFor the fabrication, PEDOT:PSS was first spin coated at \\u223c2000 rpm for 40 s on cleaned ITO-PET substrate, and annealed at 120 \\u00b0C for 10 min. Afterward, the synthesized perovskite (CH3NH3PbI3) solution was coated on annealed PEDOT:PSS\\\\/ITO-PET thin film through spin coating at the speed of \\u223c2000 rpm for 40 s with 0.45 \\u03bcm pore PVDF membrane syringe filter (Jet Biofil) at an ambient atmosphere. The obtained thin films were annealed at 100 \\u00b0C for 30 min to achieve CH3NH3PbI3\\\\/PEDOT:PSS\\\\/ITO-PET. Phenyl-C61-butyric acid methyl ester (PC61BM, 2 wt%) solution in chlorobenzene was coated at \\u223c1000 rpm to obtain PC61BM\\\\/CH3NH3PbI3\\\\/PEDOT:PSS\\\\/ITO-PET thin film. PPy solution in m-cresol (15 mg\\\\/1 ml) with 13.6 \\u03bcl Li-bis (trifluoromethanesulfonyl) imide (CF3SO2NLiSO2CF3, Li-TFSI, 28.3 mg\\\\/1 ml, TCI, >98%) and 6.8 \\u03bcl TBP (C9H13N, Aldrich, 96%) as additives was again spin-coated on PC61BM\\\\/CH3NH3PbI3\\\\/PEDOT:PSS\\\\/ITO-PET substrate at \\u223c3000 rpm for 30 s, and dried at 100 \\u00b0C for 15 min. Finally, Ag contacts (thickness \\u223c100 nm) were made by the thermal evaporation to achieve the flexible perovskite solar cell as Ag\\\\/PPy\\\\/PC61BM\\\\/CH3NH3PbI3\\\\/PEDOT:PSS\\\\/ITO-PET.\\n\\nThe atomic force spectroscopy (AFM, Nanoscope IV, Digital Instruments, Santa Barbara, USA) was used to investigate the morphology of PPy\\\\/PC61BM\\\\/CH3NH3PbI3\\\\/ITO-PET and CH3NH3PbI3\\\\/ITO-PET thin films. The confocal images of PPy\\\\/PC61BM\\\\/CH3NH3PbI3\\\\/ITO-PET and CH3NH3PbI3\\\\/ITO-PET thin films were characterized by Confocal Laser Scanning Microscope (LSM 510 META, Carl Zeiss, Germany). The crystalline nature and phases of PPy\\\\/PC61BM\\\\/CH3NH3PbI3\\\\/ITO-PET and CH3NH3PbI3\\\\/ITO-PET thin films were studied by X-ray powder diffraction (XRD, Rigaku, Cu K\\u03b1, \\u03bb = 1.54178 \\u00c5) in the Bragg angle ranging between 10\\u00b0 and 60\\u00b0 and the optical properties of the deposited thin film were demonstrated by UV\\u2013Vis spectrophotometer (JASCO, V-670, Japan). The current density (J)\\u2013voltage (V) measurements were performed for elucidating the performance of the flexible perovskite solar cell using computerized digital multimeter (model 2000, Keithley) with a variable load under one sun (1.5 AM at 100 mW\\\\/cm2). The simulated sunlight was supplied by using metal halide lamp of 1000 W and the light intensity was adjusted to \\u223c100 mW\\\\/cm2 (1.5 AM), using Si photo detector fitted with a Ka-5 filter as a reference (calibrated at NREL, USA). The incident photon-to-current conversion efficiency (IPCE) was carried out by a specially designed IPCE system for solar cell by PV measurements, Inc., USA. Before performing the IPCE measurements, the system was calibrated with a silicon photodiode, using the NIST-calibrated photodiode G425 as standard. The IPCE results of the flexible perovskite solar cell were collected as a function of wavelength from \\u223c400 to 800 nm using 75 W Xe lamp as a light source for generating monochromatic beam at a low chopping frequency. The charge collection efficiency and photoelectron density were revealed by using intensity-modulated photocurrent spectroscopy (IMPS) and intensity-modulated photovoltage spectroscopy (IMVS) using IVIUM technologies (CompactStat.e20250, USA).\\n\\n\",\r\n    \"MAI (Methyl ammonium iodide, 99.99%), PbI2 (99.9985%) were purchased and used as is to make precursors for MAPbI3 perovskites. DMF (Dimethylformamide, 99.5%), DMSO (Dimethyl sulfoxide, 99.8%), CBZ (chlorobenzene, mono, >\\u202f99.5%) were employed as main solvents and\\\\/or anti-solvents. For charge transport materials, poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT: PSS, PVP AI 4083) as a hole transport layer (HTL) and Phenyl-C61-butyric acid methyl ester (PCBM, 99.5%, Nano-C) as an electron transport layer (ETL) were used as is. In addition, NiOx precursor solution was made using Ni(NO3)2\\u00b76H2O (99.999%), ethyleneglycol (99.5%), and ethylenediamine (EDA, 99.0%).\\n\\nFor characterization of the solution processed NiOx HTL, it was coated on bare glass or ITO substrates. First, NiOx precursor solutions with various EDA additive concentration (0, 2.5, 5.0, 6.7, 7.5, 10.0\\u202fv\\\\/v %) were made by dissolving nickel nitrate hexahydrate (Ni(NO3)2\\u00b76H2O) of 0.291\\u202fg in ethyleneglycol of 1\\u202fmL. The solutions were stirred at room temperature for 12\\u202fh. The image of resultant solutions is shown in Fig. 1. The NiOx precursor solutions with various EDA concentration (0\\u201310.0%) were coated onto each substrate at 4000\\u202frpm for 90\\u202fs and annealed at 300\\u202f\\u00b0C for 60\\u202fmin in air-ambient.\\n\\nITO glass substrates (15\\u202f\\u03a9\\u00b7sq\\u22121) were cleaned with a sequential step of acetone, methyl alcohol, and isopropyl alcohol for 10\\u202fmin, respectively. After drying them in an oven, UV-ozone treatment for hydrophilic surfaces was made for 20\\u202fmin. Then PEDOT: PSS (PVP AI 4083) solution was spin-casted on the substrates at 4000\\u202frpm for 50\\u202fs and annealed at 140\\u202f\\u00b0C in air-ambient. Regarding perovskite precursor, MAPbI3 (50\\u202fwt%) perovskite solution was made by dissolving MAI (0.286\\u202fg) and PbI2 (0.830\\u202fg) 1\\u202fmL DMF with DMSO (128\\u202f\\u03bcL), and stirred at 65\\u202f\\u00b0C for 12\\u202fh. Afterward, MAPbI3 perovskite precursors (filtered with a 0.45\\u202f\\u00b5m PVDF filter) were spin-casted on the PEDOT: PSS or NiOx HTLs in a glovebox. And then, the PC61BM solution was spin-coated onto the perovskite films at 400\\u202frpm for 1\\u202fs and 1500\\u202frpm at 35\\u202fs in the glovebox too. Finally, silver electrode was thermally-evaporated under high vacuum through a shadow mask. The active area of solar cells was 4\\u202fmm2.\\n\\nOptical transmittance spectra of the various HTLs were characterized by ultraviolet-visible (UV\\u2013Vis) spectrophotometry (UV-2700; Shimadzu). Fourier transform infrared (FT-IR) measurement was performed to analyze film components by using the equipment (Vertex 80\\u202fv; Bruker) with a detector detector (mercury-cadmium-telluride: MCT) and a beam-splitter (KBr). The FT-IR was measured with scanning 128 times under a resolution of 2\\u202fcm\\u22121. The film thicknesses were measured by a surface profiler (D-100; KLA Tencor). Surface morphologies of the various NiOx HTLs were analyzed by using atomic force microscopy (AFM) (SA-AFM; Proves Inc.). Electrical resistivity of those NiOx films were estimated by preparing patterned Ag-electrodes on film surfaces, and following current-voltage sweeping was made with using a parameter analyzer. All current density-voltage (J-V) curves of the fabricated perovskite solar cells were measured by a solar simulator (Polaronix K201; McScience) under an AM 1.5 standard condition in air-ambient (100\\u202fmW\\\\/cm2, relative humidity =\\u202f20\\u201330%, 25\\u202f\\u00b0C).\\n\\n\",\r\n    \"Methyl ammonium iodide (CH3NH3I) and lead iodide (PbI2) were purchased from Sigma Aldrich and stored in the inert atmosphere. Indium doped tin oxide (ITO) coated glass substrates were purchased from M\\\\/S Global Nanotech. Poly(3,4-ethylenedioxythiophene):polystyrene sulfonic acid (PEDOT:PSS) was obtained from Sigma Aldrich and stored in 30\\u202f\\u00b0C. All other solvents were obtained from Sigma-Aldrich (St. Louis, MO) and used as received. UV\\u2013Vis absorption of perovskite thin film was recorded with a Perkin Elmer lambda 950 UV\\u2013Vis spectrometer.\\nThe steady state photoluminescence spectra and time resolved photoluminescence spectra were recorded by exciting the samples with a 355\\u202fnm line of Nd:YAGlaser with pulse width of 840\\u202fps, repetition rate of 1000\\u202fHz, and power range 1\\u20135\\u202f\\u00b5W\\\\/cm2.The spectra were recorded using Andor i-Star gated i-CCD that has a minimum gate width of 700\\u202fps with variable gate-delay technique to get a intensity variation of over 4\\u20135 orders of magnitude. XRD pattern was recorded with (Bruker DA advanced XRD equipped with CuK\\u03b1 radiation at room temperature) using graphite monochromatic Cu K\\u03b1 radiation at a scanning rate of 0.1\\u00b0\\\\/s over the Bragg angle range of 5.0\\u00b0\\u201370.0\\u00b0 (2\\u03b8). The surface morphology and microstructures of the perovskite thin film was studied by FESEM instrument operated at accelerating voltage of 15\\u202fkV. The current density\\u2013voltage (J\\u2013V) characteristics of PSC devices were measured using a Keithley 2400 source measure unit.\\n\\nPrecursor solution of MAI was synthesized using previously reported method described elsewhere [21].The perovskite precursor solution was prepared by mixing equal molar ratio of MAI and PbI2 in polar solvent DMF. ITO coated glass substrates were patterned by wet etching utilizing Zn and HCl and subsequently cleaned with soap solution, DI water, ethanol, acetone and isopropanol respectively for 15\\u202fmin each followed by ozone treatment for 15\\u202fmin. PEDOT:PSS\\\\/deionized water (1:3 v\\\\/v) solution was filtered through 0.45\\u202f\\u00b5m filter and spin-coated at 4000\\u202frpm onto the patterned substrates for 50sec, the prepared thin film was then baked, at 150\\u202f\\u00b0C for 15\\u202fmin in air. Precursor solution (CH3NH3I\\\\/PbI2 in DMF) was spin coated at 3000\\u202frpm on PEDOT: PSS covered substrate for 30\\u202fs (under ambient condition). Subsequently, chlorobenzene solution (150\\u202f\\u00b5l) were dripped onto the substrate followed by annealing at 100\\u202f\\u00b0C for 10\\u202fmin to get more compact and larger grain size of perovskite crystal. The schematic of the method is shown Fig. 1 . The standard thermally annealed film was also prepared for comparison.\\n\\nThe prototype solar cells devices were prepared in p-i-n geometry in ITO\\\\/PEDOT:PSS\\\\/MAPbI3\\\\/C60\\\\/BCP\\\\/Al architecture. To prepare the devices a 30\\u202fnm layer of C60 and 5\\u202fnm thick layer of BCP was deposited at high vacuum conditions. The current density\\u2013voltage (J\\u2013V) characteristics of PSCs were measured using a Keithley 2400 source measure unit. The solar cell performance was characterized under illumination by an Air Mass 1.5 Global (AM 1.5 G) solar simulator with an irradiation intensity of 100 mW cm-2 scanning the devices in the range of \\u22122V to 1\\u202fV. Hysteresis of the device was tested by doing a forward and backward scan between \\u22122V and 1\\u202fV.\\n\\n\",\r\n    \"After clean the ITO coated glass substrates (Samsung Corning Co.) with detergent and deionized water (DI) water, sonication in DI water, acetone, and isopropanol was carried out sequentially. Before the preparation of HTLs, substrates were treated with UV\\\\/O3 plasma for 20\\u202fmin to make hydrophilic surface. Conventional PEDOT: PSS and sol-gel derived NiOx was used as HTLs to find the effect of HTLs on performance and stability. Commercialized PEDOT:PSS (Heraeus, CleviosTM P VP AI 4083) was spin-coated by two-step (at 500\\u202frpm for 5\\u202fs and 5000\\u202frpm for 40\\u202fs) and annealed at 120\\u202f\\u00b0C for 10\\u202fmin in air. For the sol-gel derive NiOx HTLs, 0.1\\u202fM nickel acetate (Sigma-Aldrich) mixed in ethanol with 6\\u202fvol % ethanolamine was spin-coated at 3000\\u202frpm for 40\\u202fs using precursor solution followed by annealing at 350\\u202f\\u00b0C for 30\\u202fmin in air. Then, the perovskite layer was spin-coated at 500\\u202frpm for 5\\u202fs and 5000\\u202frpm for 45\\u202fs using 35\\u202fwt% solution of CH3NH3I and PbI2 with a 1:1\\u202fM ratio in N, N-dimethylmethanamide (DMF) in a glove box filled with N2. During the second step of spin-coating process, 0.7\\u202fml toluene was dropped to obtain high quality perovskite films. Thermal annealing was performed at 100\\u202f\\u00b0C for 10\\u202fmin. The PCBM solution (20\\u202fmg PCBM in 1\\u202fml chlorobenzene) was spin-coated at 1000\\u202frpm for 60\\u202fs on perovskite films. To modify the interface of PCBM\\\\/semitransparent metal layer, 0.5\\u202fwt% PEIE in methanol was spin-coated at 5000\\u202frpm for 40\\u202fs. Finally, Cu (8\\u202fnm) and Ag (8\\u202fnm) were thermally evaporated as top metal electrodes, respectively, in vacuum of 10 \\u22126\\u202fTorr.\\nOptical transparency and electrical conductivity of thin metal top electrodes were characterized by using UV\\u2013vis spectrophotometer (Varian AU\\\\/DMS-100S) and 4-point-probe measurement (FPP-RS9, Dasol Eng.). Valence bands (VBs) of PEDOT:PSS and NiOx HTLs were measured using ultraviolet photoelectron spectroscopy (UPS, ESCALAB 210) with a He I (21.2\\u202feV) source. The photocurrent density-voltage (J-V) curves were obtained using a Keithley 2400 under the condition of 100\\u202fmW\\\\/cm2 illumination and AM 1.5\\u202fG condition after calibration of light intensity with certified reference silicon solar cell. To study performance deviation in a batch, 4 devices were fabricated in each condition and characterized. Statistics analysis was performed by characterizing 28 devices for each condition. Also, change in performance with exposure time in atmospheric condition was recorded without any encapsulation (samples are kept in atmospheric condition, not under the continuous illumination). Field-emission scanning electron microscopy (FE-SEM, HITACHI-SU8220) was used to observe device structure after stability test.\\n\",\r\n    \"N, N-dimethylformamide (DMF, 99.8%) was achieved from Alfa-Aesar. Chlorobenzene (CBZ, 99.8%) and dimethylsulphoxide (DMSO, 99.7%) were purchased from J&K Scientific. [6,6]-phenyl-C61-butyric acid methyl ester (PCBM, 95%) was bought from American Dye Sources. 2,2\\u2032,7,7\\u2032-tetrakis (N, N-di-p-methoxyphenylamine)-9,90-spirobifluorene (spiro-OMeTAD, 99.8%), lead iodide (PbI2, 99.9%), and CH3NH3I (MAI, 95%) were purchased from Xi'an p-OLED. Other reagents including poly(methyl methacrylate) (PMMA, M.W. 35000), TiCl4 (Chemical pure)were supplied by Sinopharm Chemical Reagent.\\n\\nThe perovskite (PVSK) precursor (1.0\\u202fM) was prepared by dissolving 1.383\\u202fg PbI2 and 0.477\\u202fg MAI in 3\\u202fml mixture of DMSO and DMF (v\\\\/v\\u202f=\\u202f3:7), then the mixture was stirred at 70\\u202f\\u00b0C for more than 6\\u202fh and filtered with 0.45\\u202f\\u03bcm PTFE filter. The CH3NH3PbI3 (MAPbI3) perovskite film was deposited by spin-coating the precursor solution on the substrates at 1000\\u202frpm for 5\\u202fs and at 3000\\u202frpm for additional 30\\u202fs. During the second step, about 130\\u202f\\u03bcl chlorobenzene (S1) was dropped to wash the wet film. For spiro-OMeTAD containing sample (S2), chlorobenzene was replaced by spiro-OMeTAD CBZ solutions with various concentration, which are prepared by diluting from 100\\u202fmg\\\\/ml spiro-OMeTAD solution. For PMMA containing sample (S3), various amounts of PMMA were added into spiro-OMeTAD solution with optimized concentration, which were used to wash perovskite films instead. Table S1 illustrates how to prepare these solutions. After that, the perovskite film was annealed at 100\\u202f\\u00b0C for 12\\u202fmin. All these procedures were finished in a N2 filled glovebox.\\nSupplementary data associated with this article can be found, in the online version, at https:\\\\/\\\\/doi.org\\\\/10.1016\\\\/j.jcis.2018.07.100.\\nThe perovskite (PVSK) precursor (1.0\\u202fM) was prepared by dissolving 1.383\\u202fg PbI2 and 0.477\\u202fg MAI in 3\\u202fml mixture of DMSO and DMF (v\\\\/v\\u202f=\\u202f3:7), then the mixture was stirred at 70\\u202f\\u00b0C for more than 6\\u202fh and filtered with 0.45\\u202f\\u03bcm PTFE filter. The CH3NH3PbI3 (MAPbI3) perovskite film was deposited by spin-coating the precursor solution on the substrates at 1000\\u202frpm for 5\\u202fs and at 3000\\u202frpm for additional 30\\u202fs. During the second step, about 130\\u202f\\u03bcl chlorobenzene (S1) was dropped to wash the wet film. For spiro-OMeTAD containing sample (S2), chlorobenzene was replaced by spiro-OMeTAD CBZ solutions with various concentration, which are prepared by diluting from 100\\u202fmg\\\\/ml spiro-OMeTAD solution. For PMMA containing sample (S3), various amounts of PMMA were added into spiro-OMeTAD solution with optimized concentration, which were used to wash perovskite films instead. Table S1 illustrates how to prepare these solutions. After that, the perovskite film was annealed at 100\\u202f\\u00b0C for 12\\u202fmin. All these procedures were finished in a N2 filled glovebox.\\n\\nFTO substrates were firstly patterned by etching with Zn powders and diluted HCl aqueous solution. Then the as-patterned FTO were cleaned by ultra-sonicating successively with diluted Hellmanex detergent, deionized water, acetone and ethanol, finally treated with UV-Ozone for 15\\u202fmin. The FTO substrates were treated 0.04\\u202fM TiCl4 aqueous solution, which was kept in a water-bath kettle at 70\\u202f\\u00b0C for 30\\u202fmin. After that, the FTO substrates were washed with deionized water and ethanol, dried with clean N2 and heated at 130\\u202f\\u00b0C for 30\\u202fmin. To deposit the PCBM modification layer, a certain volume of PCBM solution (20\\u202fmg\\\\/ml, dissolved in CBZ) was spin-coated on FTO substrates at 3000\\u202frpm for 30\\u202fs, then the substrates was heated at 70\\u202f\\u00b0C to evaporate CBZ. Perovskite films were deposited on those substrates according to the above procedure. Finally, an Au counter electrode was directly evaporated on top of perovskite GHJ films to finish solar cells.\\n\\nMorphologies of the perovskite films were observed using atomic force microscopy (AFM, Veeco) and field emission SEM (FE-SEM, Quanta F250, JEOL Inc., Japan). X-ray diffraction (XRD, D\\\\/max 2400 X Series, Rigaku, Japan) were adopted to study the crystallinity of perovskite films. The chemical compositions of perovskite\\\\/spiro-OMeTAD GHJ films were determined with X-ray photoelectron spectroscopy (ESCALAB 250Xi, Thermo Fisher) using the He I emission line (21.2\\u202feV). UV\\u2013vis\\u2013NIR absorption spectra of the films were measured by a JASCO V-570 UV\\\\/VIS\\\\/NIR spectrometer. The current density\\u2013voltage (J-V) characteristics curves under AM 1.5G simulated solar illumination were measured using a PVIV-201V I-V Station (Newport Oriel), and the prepared devices were reversely (1.2\\u202fV\\u202f\\u2192\\u202f\\u22120.1\\u202fV) and forwardly (\\u22120.1\\u202fV\\u202f\\u2192\\u202f1.2\\u202fV) scanned with a time interval of 100\\u202fms. External quantum efficiency (EQE spectra) of solar cells were measured using a Qtest Station 1000ADX system (Growntech, Inc.) at AC mode, and the incident monochromatic light was chopped at approximately 180\\u202fHz.\\n\\n\",\r\n    \"The indium tin oxide (ITO)-coated glass substrates (15 \\u03a9\\u00a0sq\\u22121, Luminescence tech. Corp.) were cleaned through sequential ultrasonic treatments with detergent, ultrapure water, acetone and methanol for 15\\u202fmin each. Prior to electrodeposition, a 0.25\\u202fM zinc acetate (Zn(CH3COO)2, Wako) in methanol:water (10:1) solution was spin-coated onto UV\\u2013O3-treated ITO-glass substrate at 1500\\u202frpm for 30\\u202fs. After drying at 100\\u2009\\u00b0C for 15\\u202fmin, the films were then annealed at 350\\u2009\\u00b0C for 20\\u202fmin to form ZnO compact layer .\\nA three-electrode electrochemical configuration was employed for the synthesis of ZnO nanorods . The seeded ITO-glass substrate acted as the working electrode, a zinc wire operated as the counter electrode, and saturated calomel electrode (SCE) worked as the reference electrode. The substrates were fixed to a rotating electrode with a constant rotation speed of 100 rotations per minute (rpm). The deposition bath was maintained at 70\\u2009\\u00b0C containing 0.05\\u202fM KCl (99.5%, Nacalai Tesque) and 5\\u202fmM ZnCl2 (98%, Nacalai Tesque). The electrolyte was saturated with pure O2 by bubbling through a glass frit before and during the growth process. The effective area of the electrodeposited surface was about 1.54\\u00a0cm2. Electrodeposition was performed at a constant applied voltage of \\u22121.0\\u202fV\\\\/SCE for 10\\u221220\\u202fmin using a Hokuto Denko HSV-110 potentiostat. After deposition, the samples were immediately rinsed with deionized water and annealed at 350\\u2009\\u00b0C for 1\\u202fh. Finally, the samples were transferred to a nitrogen-filled glove box for perovskite deposition.\\n\\nThe CH3NH3PbI3 layer was deposited on top of ZnO nanostructures using fast deposition crystallization as reported in the literature . The perovskite precursor solution (45 wt%) was prepared by mixing 1:1\\u00a0mol ratio of PbI2 (99.999%, Wako) and CH3NH3I (98.0%, Wako), respectively, in 1\\u202fmL of anhydrous N,N-dimethylformamide (DMF, Wako). Then, a 60\\u00a0\\u00b5L of this perovskite precursor solution was spin coated on top of electrodeposited ZnO nanorods for 30\\u202fs. The substrates were spun at 5000\\u202frpm and after 8\\u202fs, 50\\u00a0\\u00b5L of toluene was quickly dropped onto the center of the substrate and followed by thermal annealing at 70\\u2009\\u00b0C for 10\\u202fmin. After cooling at room temperature, 60\\u00a0\\u00b5L of rubrene in toluene solution (5\\u202fmg\\u00a0mL\\u22121) was spin-coated on top of the perovskite layer and the films were placed in a vacuum chamber for 15\\u202fmin. Subsequently, P3HT (Sigma Aldrich) in chlorobenzene solution (15\\u202fmg\\u00a0mL\\u22121, Wako) was spin-coated at 1500\\u202frpm for 120\\u202fs. For complete drying of P3HT layer, the samples were then stored in nitrogen-filled glove box for 12\\u202fh in dark. Finally, 50\\u202fnm Ag electrodes were deposited by thermal evaporation under a base pressure of 2\\u00a0\\u00d7\\u00a010\\u22124\\u202f\\u00a0Pa. The active area of the devices is 0.09\\u00a0cm2. The solar cell devices were completed by putting silver paste in the electrode areas and stored again in vacuum to dry up before measurements.\\n\\nThe top-view and cross-sectional images were taken by a low-vacuum scanning electron microscope (SEM, Hitachi SU6600). The focused ion beam-assisted (Hitachi FB2200) cross-sectional SEM image and elemental EDX mapping analysis were obtained through ultra-high-resolution field emission scanning electron microscope (UHR FE-SEM, Hitachi SU9900). Atomic force microscopy (AFM) images were taken using a scanning probe microscope (Seiko SPA-400). Raman scattering measurement was performed at room temperature using a JASCO NRS-4100 Raman Spectrometer. The XRD patterns were characterized by a Rigaku X-ray diffractometer (RINT-TTR III) with CuK \\u03b1 radiation (\\u03bb\\u202f=\\u202f1.542\\u202f\\u00c5). The optical transmission and absorption spectra of the films were obtained on a UV\\u2013vis spectrophotometer (JASCO V-530). Photoluminescence spectra were measured under ultraviolet excitation (\\u03bbex\\u202f=\\u202f365\\u202fnm) using a high-pressure mercury-vapour light source (Olympus BH2-RFL-T3) coupled with a microscope (Olympus BX51) and a CCD spectrometer (Hamamatsu PMA-12). Current-voltage (J-V) curves were recorded from a Keithley 2611B System Source Meter unit under AM 1.5\\u202fG illumination (100\\u202fmW\\u00a0cm\\u22122, Bunko\\u2013Keiki, CEP-2000RP). The external quantum efficiency (EQE) spectra were obtained under illumination of monochromatic light using the same system at an intensity of 1.25\\u202fmW\\u00a0cm\\u22122.\\n\\n\",\r\n    \"FTO coated glass with sheet resistance of 15\\u00a0\\u03a9\\\\/sq was purchased from Ying Kou You Xuan Trade Co. Ltd. Poly(3,4 ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) aqueous solution (Clevious PVP AI 4083) was purchased from Shanghai Mater Win New Materials Co., Ltd. 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP), phenyl-C61-butyric acid methyl ester (PC61BM) and Methylammonium iodide (MAI) were purchased from Xi'an Polymer Light Technology Corp. All of the other materials were purchased from Sigma-Aldrich, including 2-propanol (IPA, 99.5%), sulfoxide (DMSO, 99.5%), N,N-dimethylformamide (DMF, 99.5%), chlorobenzene (CB, 99.5%), poly(4-styrenesulfonic acid) (PSSH), PbI2 (99.999%), ethanolamine (EA, 99%) and nickel (II) acetate tetrahydrate (99.99%). These commercially available materials were used directly without further purification.\\n\\nThe NiOx films were prepared according to a previously reported procedure . Briefly, 0.1\\u202fmmol Ni(Ac)2\\u00b74H2O was dissolved in 1.0\\u202fmL of isopropanol with ethanolamine (NH2CH2CH2OH). The mole ratio of Ni2+\\\\/EA in solution was maintained at 1:1. The solution was kept in a sealed glass vial and stirred for 4\\u00a0h in air at 75 \\u00b0C until deep green solution was obtained. The NiOx precursor solution filtered with 0.45\\u202f\\u00b5m polytetrafluoroethylene (PTFE) filters before device fabrication. NiOx film was formed by spin-coating at 1500\\u202frpm for 30\\u202fs on a FTO substrate, and annealed at 280 \\u00b0C for 1\\u202fh in air.\\n\\nThe modified PEDOT:PSS solution was prepared by adding PSSH into PEDOT:PSS solution in volume ratio of 1:4. The modified PEDOT:PSS solution was stirred for 10\\u202fmin at room temperature then filtered with 0.45\\u202f\\u00b5m polytetrafluoroethylene (PTFE) filters before device fabrication. PEDOT:PSS film was formed by spin-coating a PEDOT:PSS mixed solution at 5000\\u202frpm for 35\\u202fs on a FTO substrate, and annealed at 150 \\u00b0C for 20\\u202fmin in air.\\n\\nThe as-prepared perovskite precursor solution was prepared by PbI2 and MAI with mole ratio of 1:1 with concentration of 1\\u202fM in a mixture of DMF and DMSO (The volume fraction of DMSO is respectively 0, 15%, 30% and 45%) then was filtered using 0.45\\u202f\\u00b5m PTFE filter. The MAPbI3 (MA=methyl ammonium) perovskite thin films were fabricated by blade-coating onto HTL-coated (PEDOT:PSS and NiOx) substrates under ambient condition with RH\\u223c45%. In brief, the blade was operated at 25\\u202fmm\\\\/s with the blade gap of 100um, and the substrate temperature was maintained at 135 \\u00b0C. The resulting films on FTO glass were sequentially annealed at 90 \\u00b0C for 15\\u202fmin. Then, PC61BM solution in chlorobenzene (20\\u202fmg\\\\/mL, filtered with a 0.45\\u202f\\u00b5m PTFE filter, 40 \\u00b5L) was spin-coated onto perovskite film at 2000\\u202frpm for 30\\u202fs in the glove box filled with nitrogen. After coating, the device was set aside for half an h before next step. Then, BCP solution (0.5\\u202fmg\\\\/mL, 80\\u00a0\\u00b5L) in isopropanol was spin-coated onto PC61BM films at 4000\\u202frpm for 30\\u202fs. Finally, 120\\u202fnm thick silver electrode was deposited by thermal evaporation 1.0\\u202f\\u00d7\\u202f10\\u22124\\u202fPa through a shadow mask.\\n\\nThe morphology of perovskite films was characterized by scanning electron microscopy (SEM, TESCAN MIRA3), at a 10\\u202fkV accelerating voltage. The optical properties of samples were measured on a UV\\\\/vis\\\\/NIR spectrophotometer equipped with an integrating sphere (PerkinElmer Lambda 950). Photocurrent density-voltage (J-V) curves were measured under AM 1.5\\u202fG one sun illumination (100\\u202fmW\\\\/cm2) with a solar simulator (Enlitech SS-F7-3A) equipped with a 300\\u202fW xenon lamp and a Keithley 2400 source meter. The light intensity was adjusted by an NREL-calibrated Si solar cell. The active area of studied devices is 1.5\\u202f\\u00d7\\u202f1.5\\u00a0mm2, it defined as 0.1 mm2 by a shadow mask with spherical aperture for the J-V measurements. The XRD spectra of the prepared films were measured using a Bruker eco D8 with 40\\u202fkV and 25\\u202fmA. Film thickness is measured by KLA Tencor d-120. Contact angle is measured by AST VCAoptima.\\n\\n\",\r\n    \"Lead iodide (PbI2, 99.9985%% metals basis) and cesium iodide (CsI, 99.99% metals basis) were purchased from Alfa Aesar. Lead bromide (PbBr2, 99.999% trace metals basis) and aluminum oxide nanoparticles (Al2O3, <50\\u202fnm particle size, 20 wt% in isopropanol) were purchased from Sigma-Aldrich. Methylammonium bromide (MABr), formamidine Hydroiodide (FAI), bathocuproine (BCP), and PTAA were purchased from Xi'an Polymer Light Technol. Corp. Poly-TPD, P3HT, [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) were purchased from Lumtec. Organic solvents including anhydrous N,N-dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), chlorobenzene (CB), ethyl acetate (EA) and isopropanol were purchased from Sigma-Aldrich. All commercial materials were used as received.\\n\\nTriple-cation mixed halide perovskite precursor solution with the formula of Cs0.05(FA0.82MA0.14)0.95Pb(I0.85Br0.15)3 was prepared according to the reference with some modifications . Specifically, a 1.5\\u202fM of FAPbI3 (FAI, 234.7\\u202fmg; PbI2, 691.5\\u202fmg) and a 1.5\\u202fM of MAPbBr3 (MABr, 152.84\\u202fmg; PbBr2, 550.5\\u202fmg) dissolved in 4:1 V:V dimethylformamide (DMF)\\\\/dimethyl sulfoxide (DMSO) were first prepared. The two precursor solutions were placed on a hot plate and heated to 60 \\u00b0C until the powder dissolved completely. The final perovskite solution was prepared by mixing the FAPbI3 and MAPbBr3 precursor solutions in a 6:1 volume ratio and then adding 35\\u00a0\\u00b5L of CsI stock solution (390\\u202fmg in 1\\u202fmL DMSO). The perovskite solution stirred more than 2\\u202fh before use. It is noted that the lead is 9% mole ratio excess in the triple-cation perovskite system.\\n\\nITO glass substrates were sequentially cleaned with 2% Hellmanex solution, deionized water, anhydrous ethanol, acetone and isopropanol in an ultrasonic bath for 10\\u202fmin each, followed by plasma cleaner treatment for 10\\u202fmin. The interface PTAA (1.5\\u202fmg\\u00a0mL\\u22121 in CB), Poly-TPD (1.5\\u202fmg\\u00a0mL\\u22121 in CB) and P3HT (2\\u202fmg\\u00a0mL\\u22121 in CB) solutions were spin-coated on the ITO surface at 6000\\u202frpm for 30\\u202fs with 3\\u202fs acceleration time. The prepared interface layers were annealed at 100 \\u00b0C for 10\\u202fmin to drying the solvent. Afterwards, Al2O3 nanoparticles with desired concentrations (1:10, 1:25, 1:50, 1:75, 1:100 V:V diluted in isopropanol) were spin-coated on top of the interface layers. Prior to deposition of perovskite layer, the entire stack was annealed at 120 \\u00b0C for 20\\u202fmin in air. To prepare the perovskite absorber layer, the substrates were taken into the N2-filled glovebox. 80\\u00a0\\u00b5L perovskite solution was dropped on top of the interface layers and spin-coated at 6000\\u202frpm for 30\\u202fs with an acceleration rate of 2000\\u202frpm\\\\/s for 3\\u202fs. 10\\u202fs before the end of the spin coating, 200\\u00a0\\u00b5L of ethyl acetate was dropped to the rotating perovskite precursor film. Subsequently, the entire substrate was annealed on a hot plate at 100 \\u00b0C for 30\\u202fmin. Having deposited the perovskite layer, 70\\u00a0\\u00b5L PCBM (15\\u202fmg\\u00a0mL\\u22121 in CB) and 90\\u00a0\\u00b5L BCP (saturated solution in isopropanol) were sequentially spin-coated at 2000\\u202frpm for 30\\u202fs and at 4000\\u202frpm for 30\\u202fs, respectively. To complete the device, 120\\u202fnm thick Ag was thermally deposited. The active area of the solar cells is 9\\u00a0mm2 which is defined by overlapping of the bottom ITO and top Ag electrodes.\\n\\nOptical absorption measurements were performed on an Agilent Cary 5000 spectrophotometer. Morphologies of the Al2O3 nanoparticles and perovskite films were imaged with a scanning electron microscope (SEM, FEI Apreo LoVac). The structural property of the perovskite films was analyzed by a Bruker D8 Advance X-ray diffractometer (XRD) using Cu K\\u03b1 as the radiation source. The water contact angles of HTMs were measured by a Micro Capture Pro coupled with Image J software. The transient photovoltage decay characteristics were measured using an electrochemical workstation (ZAHNER, Germany). The current density\\u2013voltage (J-V) characteristics and steady-state output of the all solar cells were measured using a Keithley 2400 source meter. The illumination was provided by a Newport Oriel 92,192 solar simulator with an AM1.5\\u202fG filter, operating at 100\\u202fmW\\u00a0cm\\u22122, which was calibrated by a standard silicon solar cell from Newport.\\n\\n\",\r\n    \"Fig. 1 shows the device configuration with ITO\\\\/NiO\\\\/MAPbI3\\\\/ITIC\\\\/BCP\\\\/Ag, the chemical structure of PCBM and ITIC, and the energy levels of the used materials in the PeSCs. For the fabrication of PeSCs with PCBM and ITIC, the ITO substrates were first treated with UV\\\\/O3 for 30 min. Then, the 0.1 M Nickel nitrate hexahydrate (Sigma Aldrich) dissolved in ethanol and ethanolamine was coated at 3000 rpm for 40 s onto the UV\\\\/O3-treated ITO substrates, followed by annealing at 350 \\u00b0C for 30 min. For the perovskite layer, PbI2 (Lead iodide, 99.99%, Alfa Aesar) of 0.759 g and MAI (Dyesol) of 0.262 g were dissolved in DMF (anhydrous 99.8%, Sigma-Aldrich) and Dimethyl sulfoxide (DMSO, Sigma-Aldrich) with a volume ration of 7:3. The perovskite solution was spin-coated at on the NiO layer with an average thickness of 17 nm by a consecutive two-step spin-coating process at 500 rpm for 5 s and 6000 rpm for 45 s. During the second spin-coating step, the film was treated with toluene drop-casting, followed by annealing at 100 \\u00b0C for 10 min in an N2 glove box. The corresponding perovskite layer thickness is around 250\\u2013280 nm. The electron transporting materials consisting of ITIC (1-material) with concentrations of 5, 10, 15, 20 mg ml\\u22121 dissolved in chlorobenzene were coated onto the perovskite films with spin rates of 700, 1000, 1500, and 2000 rpm for 60 s. Finally, the metal electrodes having BCP (3 nm)\\\\/Ag (80 nm) were deposited by a thermal evaporator under vacuum at 10\\u22126 Torr. The photocurrent density\\u2013voltage (J\\u2013V) power curves of the PeSCs were measured using Keithley 2400 and Class AAA-based solar simulator instruments under AM 1.5 G 100 mW\\\\/cm2 light intensity. The film properties such as the work function and surface images were investigated using scanning Kelvin probe microscopy, atomic force microscopy (AFM, XE7, Park system), and Field Emission Scanning Electron Microscope(FE-SEM, HITACHI S-4800).\\n\",\r\n    \"All the raw chemicals were purchased from Sigma-Aldrich (USA) and used as received. For the fabrication of the Cs2TiBr6 HP thin films, a CsBr layer of thickness \\u223c100\\u00a0nm was first deposited on the substrate by thermal evaporation. The as-deposited CsBr thin film was placed in a home-made chamber (see Figure\\u00a0S1) filled with TiBr4 vapor. The TiBr4 vapor was slowly generated by heating TiBr4 powder at 200\\u00b0C. The typical reaction time for the complete conversion of CsBr to pure-phase Cs2TiBr6 is 24\\u00a0hr when a TiO2\\\\/FTO-glass substrate is used, as discussed in the main text. The resulting Cs2TiBr6 thin films were washed using toluene to remove any possible excess TiBr4 on the film surface for subsequent characterization and device fabrication.\\n\\nXRD of the thin films was performed using a high-resolution diffractometer (D8\\u00a0Advance; Bruker, Germany) with CuK\\u03b1 radiation. UV-vis spectra were obtained using a spectrophotometer (UV-2600; Shimadzu, Japan). The morphology and EDS elemental-distribution maps of the thin film were observed in a scanning electron microscope (LEO 1530VP; Carl Zeiss, Germany) equipped with an EDS detector (Oxford Instruments, UK). The FIB (Helios 600; FEI, Hillisboro, OR) was used to etch the thin films, where the different depths were achieved by Ga+ ion bombardment. A PHI5600 XPS system was used to acquire both XPS and UPS spectra. The analysis chamber base pressures were <1\\u00a0\\u00d7 10\\u22129 torr prior to analysis. The instrument utilized a monochromated K\\u03b1 Al source for X-ray radiation at 1,486.7 eV, and a UVS 40A2 (PREVAC, Poland) UV source and UV40A power supply provided by He\\u00a01\\u03b1 excitation (He I) for UPS at 21.22 eV. Chamber pressure for UPS was maintained at <3\\u00a0\\u00d7 10\\u22128 torr. The steady-state and time-resolved PL spectra were\\u00a0recorded with a Varian Cary Eclipse fluorescence spectrophotometer operating at 395\\u00a0nm excitation. The decay rate and lifetime was determined using the two-parameter decay function fitting method (Equation\\u00a01). The fitted diffusion coefficients for electrons and holes in Equation\\u00a01 are 0.61\\u00a0cm2 s\\u22121 and 0.44\\u00a0cm2 s\\u22121, respectively, which are used to calculate the corresponding diffusion lengths using Equation\\u00a02. The pc-AFM measurements were conducted in contact mode using an MFP-3D AFM (Asylum Research, USA) with a conducting platinum-coated silicon probe (Econo-SCM-PIC, Asylum Research) and an LED light source.\\n\\nAll first-principles computations are performed based on density functional theory (DFT) methods as implemented in the Vienna ab initio simulation package (VASP 5.4; see Ju et\\u00a0al. for details). Briefly, an energy cutoff of 520 eV is employed, and the atomic positions are optimized using the conjugate gradient scheme without any symmetric restrictions until the maximum force on each atom is less than 0.02 eV \\u00c5\\u22121. The ion cores are described using the projector augmented wave method. Grimme's long-range van der Waals interaction is described using DFT-D3 correction. A 16\\u00a0\\u00d7 16\\u00a0\\u00d7 16 k-point grid is used.\\n\\nFor the fabrication of PSCs, a compact-TiO2 ETL was first deposited on pre-patterned FTO-coated glass by spray pyrolysis at 450\\u00b0C. For some PSCs, an interfacial layer of C60 layer was deposited before the deposition of the Cs2TiBr6 thin film. This C60 layer was deposited by spin-coating a solution of C60 in chlorobenzene (2\\u00a0mg\\\\/mL) at 3,000\\u00a0rpm for 40\\u00a0s on the as-prepared TiO2 substrate, followed by annealing at 100\\u00b0C for 30\\u00a0min. The Cs2TiBr6 thin film was then deposited based on the procedure described above, followed by spin-coating the HTL solution, which consisted of 10\\u00a0mg P3HT and 1\\u00a0mL of toluene solvent. Finally, the Au layer was deposited using a thermal evaporator and a shadow mask. The J-V characteristics of the PSCs were measured using a 2400 SourceMeter (Keithley, USA) under simulated one-sun AM1.5G 100 mW.cm\\u22122 intensity (Sol3A Class AAA; Oriel, Newport, USA), under both reverse (from V OC to J SC) and forward (from J SC to V OC) scans. The step voltage was 5\\u00a0mV with a 10-ms delay time per step. The maximum-power output stability of PSCs was measured by monitoring the J output at the maximum-power-point V bias (deduced from the reverse-scan J-V curves) using\\u00a0the 2400 SourceMeter. A typical active area of 0.12\\u00a0cm2 was defined using a non-reflective mask for the J-V measurements. The stable output PCE was calculated using the following relation: PCE\\u00a0= J (mA.cm\\u22122) \\u00d7 V (V)\\\\/100 (mW.cm\\u22122). A shutter was used to control the one-sun illumination on the PSC. The EQE spectra were obtained using a quantum efficiency measurement system (IQE 200B; Oriel) consisting of a xenon lamp, a monochromator, a lock-in amplifier, and a calibrated silicon photodetector. The PSC stability was evaluated by measuring the J-V characteristics of PSCs after storing the cells under constant environmental stress for a certain period of time in an environmental climate chamber (HPP110; Memmert, Germany).\\n\\n\"\r\n]"
  },
  {
    "path": "SII_MDP/data/regression360.json",
    "content": "[{\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.00\\n JV default Jsc: 0.22\\n JV default FF: 0.57\\n JV default PCE: 0.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnBr0.3I2.7\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.12\\n JV default Jsc: 0.49\\n JV default FF: 0.25\\n JV default PCE: 0.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnBr1.5I1.5\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.14\\n JV default Jsc: 3.69\\n JV default FF: 0.26\\n JV default PCE: 0.13@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnBr2.7I0.3\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.23\\n JV default Jsc: 1.32\\n JV default FF: 0.41\\n JV default PCE: 0.12@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnBr3\\n Perovskite composition short form: CsSnBr\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.19\\n JV default Jsc: 1.57\\n JV default FF: 0.34\\n JV default PCE: 0.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.21\\n JV default Jsc: 27.67\\n JV default FF: 0.29\\n JV default PCE: 1.66@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnBrI2\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.29\\n JV default Jsc: 15.06\\n JV default FF: 0.38\\n JV default PCE: 1.67@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnBr2I\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.31\\n JV default Jsc: 11.57\\n JV default FF: 0.43\\n JV default PCE: 1.56@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: CsSnBr3\\n Perovskite composition short form: CsSnBr\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li(CF3SO2)2N; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.41\\n JV default Jsc: 3.99\\n JV default FF: 0.58\\n JV default PCE: 0.95@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-nw\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD | Hydrothermal\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.80\\n JV default Jsc: 20.40\\n JV default FF: 0.63\\n JV default PCE: 10.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-nw\\n ETL additives compounds: Unknown | Er\\n ETL deposition procedure: CBD | Hydrothermal\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.83\\n JV default Jsc: 21.30\\n JV default FF: 0.64\\n JV default PCE: 11.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-nw\\n ETL additives compounds: Unknown | Er; Yb\\n ETL deposition procedure: CBD | Hydrothermal\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 21.70\\n JV default FF: 0.66\\n JV default PCE: 12.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-np\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbBr3\\n Perovskite composition short form: MAPbBr\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.11\\n JV default Jsc: 8.10\\n JV default FF: 0.58\\n JV default PCE: 5.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-np\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbBr3\\n Perovskite composition short form: MAPbBr\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.14\\n JV default Jsc: 9.60\\n JV default FF: 0.56\\n JV default PCE: 6.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-np\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbBr3\\n Perovskite composition short form: MAPbBr\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Co-TPTB; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.14\\n JV default Jsc: 9.60\\n JV default FF: 0.56\\n JV default PCE: 6.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 70; 100\\n Perovskite deposition thermal annealing time: 1.0; 8.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.85\\n JV default Jsc: 18.23\\n JV default FF: 0.81\\n JV default PCE: 12.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 70; 100\\n Perovskite deposition thermal annealing time: 1.0; 8.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.83\\n JV default Jsc: 14.44\\n JV default FF: 0.78\\n JV default PCE: 9.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 70; 100\\n Perovskite deposition thermal annealing time: 1.0; 8.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc:  \\n JV default Jsc:  \\n JV default FF:  \\n JV default PCE: 12.03@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 70; 100\\n Perovskite deposition thermal annealing time: 1.0; 8.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc:  \\n JV default Jsc:  \\n JV default FF:  \\n JV default PCE: 8.61@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.91\\n JV default Jsc: 15.77\\n JV default FF: 0.70\\n JV default PCE: 10.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.54\\n JV default Jsc: 2.02\\n JV default FF: 0.54\\n JV default PCE: 0.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 19.20\\n JV default FF: 0.65\\n JV default PCE: 13.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Sn\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09\\n JV default Jsc: 21.20\\n JV default FF: 0.70\\n JV default PCE: 16.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Sn\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 21.53\\n JV default FF: 0.73\\n JV default PCE: 17.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Sn\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.07\\n JV default Jsc: 21.08\\n JV default FF: 0.67\\n JV default PCE: 15.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 19.20\\n JV default FF: 0.65\\n JV default PCE: 13.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Sn\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 21.53\\n JV default FF: 0.73\\n JV default PCE: 17.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788MA0.162PbBr0.51I2.49\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 22.40\\n JV default FF: 0.76\\n JV default PCE: 18.45@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788GU0.032MA0.129PbBr0.51I2.49\\n Perovskite composition short form: CsFAGUMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.12\\n JV default Jsc: 23.10\\n JV default FF: 0.78\\n JV default PCE: 20.29@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788GU0.065MA0.097PbBr0.51I2.49\\n Perovskite composition short form: CsFAGUMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.11\\n JV default Jsc: 21.70\\n JV default FF: 0.76\\n JV default PCE: 18.26@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788GU0.097MA0.065PbBr0.51I2.49\\n Perovskite composition short form: CsFAGUMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 19.50\\n JV default FF: 0.73\\n JV default PCE: 15.78@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788GU0.129MA0.032PbBr0.51I2.49\\n Perovskite composition short form: CsFAGUMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.07\\n JV default Jsc: 15.90\\n JV default FF: 0.66\\n JV default PCE: 11.27@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788GU0.162PbBr0.51I2.49\\n Perovskite composition short form: CsFAGUPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 12.10\\n JV default FF: 0.59\\n JV default PCE: 7.51@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: none\\n Perovskite deposition procedure: Evaporation\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS | TPD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating | Spin-coating\\n Backcontact stack sequence: Ba | Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation | Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 16.34\\n JV default FF: 0.73\\n JV default PCE: 12.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbBr0.09I2.91\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: none >> none >> IPA\\n Perovskite deposition procedure: Co-evaporation >> Evaporation >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 5.0\\n HTL stack sequence: PEDOT:PSS | TPD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating | Spin-coating\\n Backcontact stack sequence: Ba | Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation | Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.11\\n JV default Jsc: 14.14\\n JV default FF: 0.65\\n JV default PCE: 10.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbBr0.3I2.7\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: none >> none >> IPA\\n Perovskite deposition procedure: Co-evaporation >> Evaporation >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 5.0\\n HTL stack sequence: PEDOT:PSS | TPD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating | Spin-coating\\n Backcontact stack sequence: Ba | Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation | Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.14\\n JV default Jsc: 13.14\\n JV default FF: 0.72\\n JV default PCE: 10.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbBr0.6I2.4\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: none >> none >> IPA\\n Perovskite deposition procedure: Co-evaporation >> Evaporation >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 5.0\\n HTL stack sequence: PEDOT:PSS | TPD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating | Spin-coating\\n Backcontact stack sequence: Ba | Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation | Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.13\\n JV default Jsc: 11.72\\n JV default FF: 0.70\\n JV default PCE: 9.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbBr1.2I1.8\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: none >> none >> IPA\\n Perovskite deposition procedure: Co-evaporation >> Evaporation >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 5.0\\n HTL stack sequence: PEDOT:PSS | TPD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating | Spin-coating\\n Backcontact stack sequence: Ba | Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation | Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.18\\n JV default Jsc: 3.01\\n JV default FF: 0.71\\n JV default PCE: 2.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbBr1.8I1.2\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: none >> none >> IPA\\n Perovskite deposition procedure: Co-evaporation >> Evaporation >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 5.0\\n HTL stack sequence: PEDOT:PSS | TPD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating | Spin-coating\\n Backcontact stack sequence: Ba | Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation | Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.18\\n JV default Jsc: 1.78\\n JV default FF: 0.55\\n JV default PCE: 1.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: FA0.85MA0.15PbBr0.45I2.55\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 12.50\\n JV default FF: 0.68\\n JV default PCE: 8.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: FA0.85MA0.15PbBr0.45I2.55\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: BDT0FMeDPA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 17.20\\n JV default FF: 0.67\\n JV default PCE: 11.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: FA0.85MA0.15PbBr0.45I2.55\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: BDT2FMeDPA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 21.40\\n JV default FF: 0.66\\n JV default PCE: 14.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: Cs0.05FA0.827MA0.123PbBr0.369I2.631\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120; 100\\n Perovskite deposition thermal annealing time: 10.0; 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.11\\n JV default Jsc: 22.40\\n JV default FF: 0.75\\n JV default PCE: 18.65@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: Cs0.05FA0.827MA0.123PbBr0.369I2.631\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150; 100\\n Perovskite deposition thermal annealing time: 20.0; 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.12\\n JV default Jsc: 22.82\\n JV default FF: 0.77\\n JV default PCE: 20.52@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: Cs0.05FA0.827MA0.123PbBr0.369I2.631\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150; 100\\n Perovskite deposition thermal annealing time: 20.0; 30.0\\n HTL stack sequence: 1\\u2010adamantylamine hydrochloride | Spiro-MeOTAD\\n HTL additives compounds: Unknown | Li-TSFI; TBP\\n HTL deposition procedure: Spin-coating | Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.14\\n JV default Jsc: 22.90\\n JV default FF: 0.77\\n JV default PCE: 21.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: Cs0.05FA0.827MA0.123PbBr0.369I2.631\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 120; 100\\n Perovskite deposition thermal annealing time: 10.0; 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.11\\n JV default Jsc: 22.48\\n JV default FF: 0.78\\n JV default PCE: 19.43@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: Cs0.05FA0.827MA0.123PbBr0.369I2.631\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150; 100\\n Perovskite deposition thermal annealing time: 20.0; 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.13\\n JV default Jsc: 23.01\\n JV default FF: 0.79\\n JV default PCE: 20.52@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: Cs0.05FA0.827MA0.123PbBr0.369I2.631\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150; 100\\n Perovskite deposition thermal annealing time: 20.0; 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.15\\n JV default Jsc: 23.40\\n JV default FF: 0.78\\n JV default PCE: 21.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: SnO2 | C60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Unknown | Unknown\\n Perovskite composition long form: Cs0.05FA0.788MA0.162PbBr0.3I2.7\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: Rb\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 24.30\\n JV default FF: 0.76\\n JV default PCE: 19.89@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788MA0.162PbBr0.5I2.5\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 22.28\\n JV default FF: 0.72\\n JV default PCE: 15.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788MA0.162PbBr0.5I2.5\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100; 85\\n Perovskite deposition thermal annealing time: 60.0; 720.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 22.02\\n JV default FF: 0.69\\n JV default PCE: 13.24@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788MA0.162PbBr0.5I2.5\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100; 85\\n Perovskite deposition thermal annealing time: 60.0; 1440.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.85\\n JV default Jsc: 20.25\\n JV default FF: 0.67\\n JV default PCE: 11.70@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Cs0.05FA0.788MA0.162PbBr0.5I2.5\\n Perovskite composition short form: CsFAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100; 85\\n Perovskite deposition thermal annealing time: 60.0; 2880.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.73\\n JV default Jsc: 18.40\\n JV default FF: 0.62\\n JV default PCE: 8.37@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 16.20\\n JV default FF: 0.49\\n JV default PCE: 8.09@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: N-Graphene\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 17.60\\n JV default FF: 0.54\\n JV default PCE: 9.71@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | Carbon-QDs\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 16.20\\n JV default FF: 0.49\\n JV default PCE: 8.09@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | Carbon-QDs\\n ETL additives compounds: N-Graphene | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.07\\n JV default Jsc: 19.70\\n JV default FF: 0.75\\n JV default PCE: 15.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.03\\n JV default Jsc: 18.20\\n JV default FF: 0.56\\n JV default PCE: 10.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: N-Graphene\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05\\n JV default Jsc: 19.10\\n JV default FF: 0.61\\n JV default PCE: 12.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | Carbon-QDs\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 19.40\\n JV default FF: 0.73\\n JV default PCE: 15.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | Carbon-QDs\\n ETL additives compounds: N-Graphene | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: LiMgNiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 20.60\\n JV default FF: 0.77\\n JV default PCE: 17.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | TiCl4\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 21.70\\n JV default FF: 0.72\\n JV default PCE: 17.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBr0.45I2.55\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> DMSO; Methanol\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 280\\n Perovskite deposition thermal annealing time: Unknown >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.14\\n JV default Jsc: 9.90\\n JV default FF: 0.64\\n JV default PCE: 7.22@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBr0.45I2.55\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> DMSO; Methanol\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 280\\n Perovskite deposition thermal annealing time: Unknown >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.23\\n JV default Jsc: 13.30\\n JV default FF: 0.68\\n JV default PCE: 11.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBr0.45I2.55\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> DMSO; Methanol\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 280\\n Perovskite deposition thermal annealing time: Unknown >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.25\\n JV default Jsc: 12.00\\n JV default FF: 0.62\\n JV default PCE: 9.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBr0.45I2.55\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> DMSO; Methanol\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 280\\n Perovskite deposition thermal annealing time: Unknown >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 9.00\\n JV default FF: 0.72\\n JV default PCE: 6.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | ZnO-np\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 22.90\\n JV default FF: 0.67\\n JV default PCE: 14.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 19.63\\n JV default FF: 0.71\\n JV default PCE: 12.11@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: PTAA\\n HTL additives compounds: PolyTPD\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 20.81\\n JV default FF: 0.74\\n JV default PCE: 13.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: PTAA\\n HTL additives compounds: PolyTPD\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 21.89\\n JV default FF: 0.77\\n JV default PCE: 14.63@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: PTAA\\n HTL additives compounds: PolyTPD\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 17.99\\n JV default FF: 0.72\\n JV default PCE: 11.32@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 40; 60; 70; 100\\n Perovskite deposition thermal annealing time: 5.0; 5.0; 5.0; 5.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.12\\n JV default Jsc: 20.30\\n JV default FF: 0.71\\n JV default PCE: 16.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: CdS\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 40; 60; 70; 100\\n Perovskite deposition thermal annealing time: 5.0; 5.0; 5.0; 5.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 18.70\\n JV default FF: 0.72\\n JV default PCE: 15.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: CdS\\n ETL additives compounds: Unknown\\n ETL deposition procedure: CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 40; 60; 70; 100\\n Perovskite deposition thermal annealing time: 5.0; 5.0; 5.0; 5.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.12\\n JV default Jsc: 19.70\\n JV default FF: 0.74\\n JV default PCE: 16.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | Sn\\n ETL deposition procedure: Spin-coating | Electrospraying\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: IPA >> Ethanol\\n Perovskite deposition procedure: Electrospraying >> Dropcasting\\n Perovskite deposition thermal annealing temperature: 100; 500 >> 110\\n Perovskite deposition thermal annealing time: Unknown; 20.0 >> 20.0\\n HTL stack sequence: Carbon\\n HTL additives compounds: \\n HTL deposition procedure: Electrospraying\\n Backcontact stack sequence: FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.37\\n JV default Jsc: 6.75\\n JV default FF: 0.59\\n JV default PCE: 1.47@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | Sn\\n ETL deposition procedure: Spin-coating | Electrospraying\\n Perovskite composition long form: CsSnBr0.5I2.5\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: IPA >> Ethanol\\n Perovskite deposition procedure: Electrospraying >> Dropcasting\\n Perovskite deposition thermal annealing temperature: 100; 500 >> 110\\n Perovskite deposition thermal annealing time: Unknown; 20.0 >> 20.0\\n HTL stack sequence: Carbon\\n HTL additives compounds: \\n HTL deposition procedure: Electrospraying\\n Backcontact stack sequence: FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.44\\n JV default Jsc: 6.58\\n JV default FF: 0.55\\n JV default PCE: 1.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | Sn\\n ETL deposition procedure: Spin-coating | Electrospraying\\n Perovskite composition long form: CsSnBr0.6I2.4\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: IPA >> Ethanol\\n Perovskite deposition procedure: Electrospraying >> Dropcasting\\n Perovskite deposition thermal annealing temperature: 100; 500 >> 110\\n Perovskite deposition thermal annealing time: Unknown; 20.0 >> 20.0\\n HTL stack sequence: Carbon\\n HTL additives compounds: \\n HTL deposition procedure: Electrospraying\\n Backcontact stack sequence: FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.56\\n JV default Jsc: 6.22\\n JV default FF: 0.58\\n JV default PCE: 2.02@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | Sn\\n ETL deposition procedure: Spin-coating | Electrospraying\\n Perovskite composition long form: CsSnBr2I\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: IPA >> Ethanol\\n Perovskite deposition procedure: Electrospraying >> Dropcasting\\n Perovskite deposition thermal annealing temperature: 100; 500 >> 110\\n Perovskite deposition thermal annealing time: Unknown; 20.0 >> 20.0\\n HTL stack sequence: Carbon\\n HTL additives compounds: \\n HTL deposition procedure: Electrospraying\\n Backcontact stack sequence: FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.57\\n JV default Jsc: 3.41\\n JV default FF: 0.55\\n JV default PCE: 1.08@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | Sn\\n ETL deposition procedure: Spin-coating | Electrospraying\\n Perovskite composition long form: CsSnBr2.5I0.5\\n Perovskite composition short form: CsSnBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: IPA >> Ethanol\\n Perovskite deposition procedure: Electrospraying >> Dropcasting\\n Perovskite deposition thermal annealing temperature: 100; 500 >> 110\\n Perovskite deposition thermal annealing time: Unknown; 20.0 >> 20.0\\n HTL stack sequence: Carbon\\n HTL additives compounds: \\n HTL deposition procedure: Electrospraying\\n Backcontact stack sequence: FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.57\\n JV default Jsc: 0.01\\n JV default FF: 0.37\\n JV default PCE: 0.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 7.25\\n JV default FF: 0.87\\n JV default PCE: 5.47@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: BMII\\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 21.58\\n JV default FF: 0.70\\n JV default PCE: 15.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96\\n JV default Jsc: 19.40\\n JV default FF: 0.68\\n JV default PCE: 12.58@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 80\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ca | Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sputtering | Sputtering\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.81\\n JV default Jsc: 17.70\\n JV default FF: 0.65\\n JV default PCE: 10.41@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 90\\n Perovskite deposition thermal annealing time: 110\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ca | Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sputtering | Sputtering\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.80\\n JV default Jsc: 17.42\\n JV default FF: 0.33\\n JV default PCE: 5.16@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-nt\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Hydrothermal\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: P3HT\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 17.80\\n JV default FF: 0.68\\n JV default PCE: 10.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG\\n ETL stack sequence: AZO | ZnO-nw\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Sputtering | CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70 >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.70\\n JV default Jsc: 13.80\\n JV default FF: 0.40\\n JV default PCE: 3.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG\\n ETL stack sequence: AZO | ZnO-nw\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Sputtering | CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70 >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.81\\n JV default Jsc: 16.00\\n JV default FF: 0.53\\n JV default PCE: 7.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG\\n ETL stack sequence: AZO | ZnO-nw\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Sputtering | CBD\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70 >> 100\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.78\\n JV default Jsc: 8.40\\n JV default FF: 0.36\\n JV default PCE: 2.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 60; 105\\n Perovskite deposition thermal annealing time: 45.0; 70.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 20.00\\n JV default FF: 0.65\\n JV default PCE: 13.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl; PEG\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 60; 105\\n Perovskite deposition thermal annealing time: 45.0; 70.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 23.00\\n JV default FF: 0.68\\n JV default PCE: 17.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl; PEG\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 60; 105\\n Perovskite deposition thermal annealing time: 45.0; 70.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 22.00\\n JV default FF: 0.62\\n JV default PCE: 15.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: Nb2O5 | PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBrI2\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 45; 160\\n Perovskite deposition thermal annealing time: 0.5; 2.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 14.13\\n JV default FF: 0.78\\n JV default PCE: 11.74@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBrI2\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 45; 160\\n Perovskite deposition thermal annealing time: 0.5; 2.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 13.48\\n JV default FF: 0.73\\n JV default PCE: 9.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-np | C60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBrI2\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 45; 160\\n Perovskite deposition thermal annealing time: 0.5; 2.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 13.96\\n JV default FF: 0.72\\n JV default PCE: 10.65@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: Nb2O5 | PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBrI2\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 45; 160\\n Perovskite deposition thermal annealing time: 0.5; 2.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 13.75\\n JV default FF: 0.76\\n JV default PCE: 11.17@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBrI2\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 45; 160\\n Perovskite deposition thermal annealing time: 0.5; 2.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 12.92\\n JV default FF: 0.69\\n JV default PCE: 8.31@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-np | C60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsPbBrI2\\n Perovskite composition short form: CsPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 45; 160\\n Perovskite deposition thermal annealing time: 0.5; 2.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 13.47\\n JV default FF: 0.71\\n JV default PCE: 10.16@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: Ag2CsSb2I3\\n Perovskite composition short form: AgCsSbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.77\\n JV default Jsc: 1.91\\n JV default FF: 0.67\\n JV default PCE: 0.99@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl; MoOx-np\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 22.55\\n JV default FF: 0.70\\n JV default PCE: 14.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl; MoOx-np\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 22.75\\n JV default FF: 0.74\\n JV default PCE: 15.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl; MoOx-np\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 22.77\\n JV default FF: 0.75\\n JV default PCE: 16.96@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl; MoOx-np\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 21.59\\n JV default FF: 0.72\\n JV default PCE: 14.03@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.89\\n JV default Jsc: 22.55\\n JV default FF: 0.75\\n JV default PCE: 15.15@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: FA0.6MA0.4Pb0.4Sn0.6I3 | (PEA)2Pb0.4Sn0.6I4\\n Perovskite composition short form: FAMAPbSnI | (PEA)PbSnI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 70 >> 100\\n Perovskite deposition thermal annealing time: 30.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TPB\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.77\\n JV default Jsc: 26.60\\n JV default FF: 0.76\\n JV default PCE: 15.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Rhodamine 101 | LiF\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMSO; GBL @ 4; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 18.50\\n JV default FF: 0.77\\n JV default PCE: 13.12@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Rhodamine 101 | LiF\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3 | CA2PbI4\\n Perovskite composition short form: MAPbI | CAPbI\\n Perovskite additives compounds: Cl | nan\\n Perovskite deposition solvents: DMSO; GBL @ 4; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 17.56\\n JV default FF: 0.76\\n JV default PCE: 12.64@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Rhodamine 101 | LiF\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3 | CA2PbI4\\n Perovskite composition short form: MAPbI | CAPbI\\n Perovskite additives compounds: Cl | nan\\n Perovskite deposition solvents: DMSO; GBL @ 4; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 19.29\\n JV default FF: 0.77\\n JV default PCE: 13.86@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Rhodamine 101 | LiF\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3 | CA2PbI4\\n Perovskite composition short form: MAPbI | CAPbI\\n Perovskite additives compounds: Cl | nan\\n Perovskite deposition solvents: DMSO; GBL @ 4; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 8.19\\n JV default FF: 0.68\\n JV default PCE: 5.27@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Rhodamine 101 | LiF\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3 | CA2PbI4\\n Perovskite composition short form: MAPbI | CAPbI\\n Perovskite additives compounds: Cl | nan\\n Perovskite deposition solvents: DMSO; GBL @ 4; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 4.78\\n JV default FF: 0.65\\n JV default PCE: 2.88@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Rhodamine 101 | LiF\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3 | CA2PbI4\\n Perovskite composition short form: MAPbI | CAPbI\\n Perovskite additives compounds: Cl | nan\\n Perovskite deposition solvents: DMSO; GBL @ 4; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 19.57\\n JV default FF: 0.73\\n JV default PCE: 13.17@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | Rhodamine 101 | LiF\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMSO; GBL @ 4; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 17.86\\n JV default FF: 0.73\\n JV default PCE: 13.08@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 18.48\\n JV default FF: 0.61\\n JV default PCE: 11.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 17.53\\n JV default FF: 0.57\\n JV default PCE: 9.82@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 15.98\\n JV default FF: 0.54\\n JV default PCE: 8.73@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 16.99\\n JV default FF: 0.62\\n JV default PCE: 10.38@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 18.11\\n JV default FF: 0.63\\n JV default PCE: 11.24@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 18.33\\n JV default FF: 0.62\\n JV default PCE: 11.25@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 18.19\\n JV default FF: 0.62\\n JV default PCE: 11.22@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 11.10\\n JV default FF: 0.59\\n JV default PCE: 5.58@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.97\\n JV default Jsc: 14.63\\n JV default FF: 0.53\\n JV default PCE: 7.62@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 18.11\\n JV default FF: 0.61\\n JV default PCE: 11.06@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 19.06\\n JV default FF: 0.60\\n JV default PCE: 11.24@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 20.45\\n JV default FF: 0.59\\n JV default PCE: 11.93@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 19.70\\n JV default FF: 0.60\\n JV default PCE: 11.82@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 18.04\\n JV default FF: 0.59\\n JV default PCE: 10.61@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 10.98\\n JV default FF: 0.53\\n JV default PCE: 5.54@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.17FA0.83PbBr0.51I2.49\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO >> DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 12.61\\n JV default FF: 0.55\\n JV default PCE: 6.52@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: FAPbI3\\n Perovskite composition short form: FAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 170\\n Perovskite deposition thermal annealing time: 5\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 17.63\\n JV default FF: 0.65\\n JV default PCE: 10.94@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: FAPbI3\\n Perovskite composition short form: FAPbI\\n Perovskite additives compounds: PMMA\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 170\\n Perovskite deposition thermal annealing time: 5\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 23.20\\n JV default FF: 0.71\\n JV default PCE: 16.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: FAPbI3\\n Perovskite composition short form: FAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL @ 3; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 150.0 >> 150.0\\n Perovskite deposition thermal annealing time: 10.0 >> 20.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.79\\n JV default Jsc: 18.83\\n JV default FF: 0.71\\n JV default PCE: 10.58@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: FAPbI3\\n Perovskite composition short form: FAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL @ 3; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 150.0 >> 150.0\\n Perovskite deposition thermal annealing time: 10.0 >> 20.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.82\\n JV default Jsc: 21.75\\n JV default FF: 0.78\\n JV default PCE: 14.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: FAPbI3\\n Perovskite composition short form: FAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL @ 3; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 150.0 >> 150.0\\n Perovskite deposition thermal annealing time: 10.0 >> 20.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.81\\n JV default Jsc: 17.66\\n JV default FF: 0.64\\n JV default PCE: 9.19@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: FAPbI3\\n Perovskite composition short form: FAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL @ 3; 7 >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 150.0 >> 150.0\\n Perovskite deposition thermal annealing time: 10.0 >> 20.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 20.17\\n JV default FF: 0.72\\n JV default PCE: 12.59@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spray-coating\\n Perovskite deposition thermal annealing temperature: 70.0 >> 90.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: P3HT\\n HTL additives compounds: Li-bisLi-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 15.08\\n JV default FF: 0.53\\n JV default PCE: 7.99@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spray-coating\\n Perovskite deposition thermal annealing temperature: 70.0 >> 90.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: P3HT\\n HTL additives compounds: Li-bis; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.64\\n JV default Jsc: 1.50\\n JV default FF: 0.36\\n JV default PCE: 0.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spray-coating\\n Perovskite deposition thermal annealing temperature: 70.0 >> 90.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: P3HT\\n HTL additives compounds: Li-bis; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.76\\n JV default Jsc: 4.58\\n JV default FF: 0.52\\n JV default PCE: 1.82@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spray-coating\\n Perovskite deposition thermal annealing temperature: 70.0 >> 90.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: P3HT\\n HTL additives compounds: Li-bis; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 12.39\\n JV default FF: 0.49\\n JV default PCE: 5.71@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spray-coating\\n Perovskite deposition thermal annealing temperature: 70.0 >> 90.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: P3HT\\n HTL additives compounds: Li-bis; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 13.81\\n JV default FF: 0.54\\n JV default PCE: 7.48@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spray-coating\\n Perovskite deposition thermal annealing temperature: 70.0 >> 90.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: P3HT\\n HTL additives compounds: Li-bis; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96\\n JV default Jsc: 11.09\\n JV default FF: 0.47\\n JV default PCE: 5.05@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spray-coating\\n Perovskite deposition thermal annealing temperature: 70.0 >> 90.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: P3HT\\n HTL additives compounds: Li-bis; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 7.38\\n JV default FF: 0.39\\n JV default PCE: 2.55@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 13.00\\n JV default FF: 0.59\\n JV default PCE: 7.76@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 14.20\\n JV default FF: 0.57\\n JV default PCE: 8.46@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 18.60\\n JV default FF: 0.50\\n JV default PCE: 9.43@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.89\\n JV default Jsc: 18.30\\n JV default FF: 0.54\\n JV default PCE: 8.81@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 13.70\\n JV default FF: 0.49\\n JV default PCE: 6.76@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.03\\n JV default Jsc: 12.10\\n JV default FF: 0.45\\n JV default PCE: 5.57@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 9.51\\n JV default FF: 0.21\\n JV default PCE: 2.06@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 9.83\\n JV default FF: 0.61\\n JV default PCE: 6.51@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 12.40\\n JV default FF: 0.57\\n JV default PCE: 7.29@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-70\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> Ethanol; IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 12.30\\n JV default FF: 0.62\\n JV default PCE: 8.06@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 19.18\\n JV default FF: 0.70\\n JV default PCE: 11.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 18.68\\n JV default FF: 0.65\\n JV default PCE: 10.70@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.80\\n JV default Jsc: 11.29\\n JV default FF: 0.56\\n JV default PCE: 5.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.82\\n JV default Jsc: 11.00\\n JV default FF: 0.49\\n JV default PCE: 4.43@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 15.58\\n JV default FF: 0.70\\n JV default PCE: 9.67@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 15.43\\n JV default FF: 0.70\\n JV default PCE: 9.33@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 15.21\\n JV default FF: 0.70\\n JV default PCE: 9.17@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 15.15\\n JV default FF: 0.70\\n JV default PCE: 9.13@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | AZO | Ag | AZO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 12.85\\n JV default FF: 0.70\\n JV default PCE: 7.97@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | AZO | Ag | AZO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 12.85\\n JV default FF: 0.70\\n JV default PCE: 7.95@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | AZO | Ag | AZO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 12.81\\n JV default FF: 0.70\\n JV default PCE: 7.92@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | AZO | Ag | AZO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: AgOTf-doped GO\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 12.75\\n JV default FF: 0.70\\n JV default PCE: 7.87@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.67\\n JV default Jsc: 7.74\\n JV default FF: 0.29\\n JV default PCE: 1.46@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.77\\n JV default Jsc: 9.66\\n JV default FF: 0.50\\n JV default PCE: 3.69@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.83\\n JV default Jsc: 17.57\\n JV default FF: 0.60\\n JV default PCE: 8.79@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 21.74\\n JV default FF: 0.62\\n JV default PCE: 11.58@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.82\\n JV default Jsc: 22.21\\n JV default FF: 0.54\\n JV default PCE: 9.88@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.83\\n JV default Jsc: 19.34\\n JV default FF: 0.45\\n JV default PCE: 7.33@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: HCl\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: HPbI3 | Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 85\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05\\n JV default Jsc: 21.76\\n JV default FF: 0.76\\n JV default PCE: 17.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: HCl\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 85\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.03\\n JV default Jsc: 20.84\\n JV default FF: 0.74\\n JV default PCE: 15.92@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: HCl\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 85\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 20.99\\n JV default FF: 0.68\\n JV default PCE: 14.09@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 70\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Candle soot | FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Candel burning | Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.81\\n JV default Jsc: 7.15\\n JV default FF: 0.28\\n JV default PCE: 1.73@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 70\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Candle soot | FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Candel burning | Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.84\\n JV default Jsc: 11.75\\n JV default FF: 0.46\\n JV default PCE: 4.56@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 70\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Candle soot | FTO | SLG\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Candel burning | Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 16.50\\n JV default FF: 0.67\\n JV default PCE: 9.78@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 70\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: FTO\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.50\\n JV default Jsc: 2.39\\n JV default FF: 0.31\\n JV default PCE: 0.37@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 70\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Pt-sheet\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.40\\n JV default Jsc: 0.50\\n JV default FF: 0.15\\n JV default PCE: 0.03@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 70\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Ag-sheet\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.40\\n JV default Jsc: 1.35\\n JV default FF: 0.29\\n JV default PCE: 0.16@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: Unknown >> 70\\n Perovskite deposition thermal annealing time: Unknown >> 15.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon-paper\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sandwiching\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.65\\n JV default Jsc: 1.50\\n JV default FF: 0.15\\n JV default PCE: 0.15@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 60.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 20.00\\n JV default FF: 0.79\\n JV default PCE: 16.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 60.0\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 21.96\\n JV default FF: 0.78\\n JV default PCE: 18.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: FAPbI3\\n Perovskite composition short form: FAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiMgLiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.80\\n JV default Jsc: 14.94\\n JV default FF: 0.39\\n JV default PCE: 17.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: Cs0.05FA0.95PbBr0.15I2.85\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: Undoped\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiMgLiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 19.02\\n JV default FF: 0.61\\n JV default PCE: 17.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: Cs0.1FA0.9PbBr0.3I2.7\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: Undoped\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiMgLiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 22.40\\n JV default FF: 0.76\\n JV default PCE: 17.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: Cs0.15FA0.85PbBr0.45I2.55\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: Undoped\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiMgLiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 21.88\\n JV default FF: 0.80\\n JV default PCE: 17.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: Cs0.2FA0.8PbBr0.6I2.4\\n Perovskite composition short form: CsFAPbBrI\\n Perovskite additives compounds: Undoped\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiMgLiO\\n HTL additives compounds: \\n HTL deposition procedure: Spray-pyrolys\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 21.54\\n JV default FF: 0.79\\n JV default PCE: 17.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: CsPbBr-np\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 22.50\\n JV default FF: 0.76\\n JV default PCE: 18.51@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.01MA0.99PbBr0.03I2.97\\n Perovskite composition short form: CsMAPbBrI\\n Perovskite additives compounds: CsPbBr-np\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 22.30\\n JV default FF: 0.79\\n JV default PCE: 19.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.02MA0.98PbBr0.06I2.94\\n Perovskite composition short form: CsMAPbBrI\\n Perovskite additives compounds: CsPbBr-np\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.13\\n JV default Jsc: 22.81\\n JV default FF: 0.79\\n JV default PCE: 20.46@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: Cs0.03MA0.97PbBr0.09I2.91\\n Perovskite composition short form: CsMAPbBrI\\n Perovskite additives compounds: CsPbBr-np\\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 20.52\\n JV default FF: 0.72\\n JV default PCE: 14.58@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Tetraisopropil titanate butanol | TiCl4\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 19.63\\n JV default FF: 0.58\\n JV default PCE: 9.86@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Tetraisopropil titanate butanol | TiCl4\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.85\\n JV default Jsc: 20.62\\n JV default FF: 0.57\\n JV default PCE: 10.03@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Tetraisopropil titanate butanol | TiCl4\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 19.71\\n JV default FF: 0.60\\n JV default PCE: 10.33@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Tetraisopropil titanate butanol | TiCl4\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 20.69\\n JV default FF: 0.62\\n JV default PCE: 11.24@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: ZnO-c | ZnO-nw | TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Hydrothermal | Hydrothermal\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 120.0 >> 120.0\\n Perovskite deposition thermal annealing time: 10.0 >> 10.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sputtering\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.85\\n JV default Jsc: 13.95\\n JV default FF: 0.55\\n JV default PCE: 6.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: ZnO-c | ZnO-nw\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Hydrothermal\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 120.0 >> 120.0\\n Perovskite deposition thermal annealing time: 10.0 >> 10.0\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Sputtering\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.75\\n JV default Jsc: 12.71\\n JV default FF: 0.47\\n JV default PCE: 4.49@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: ALD | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 12.74\\n JV default FF: 0.44\\n JV default PCE: 4.85@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: ALD | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 14.19\\n JV default FF: 0.48\\n JV default PCE: 6.06@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: ALD | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 18.30\\n JV default FF: 0.40\\n JV default PCE: 7.03@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: ALD | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96\\n JV default Jsc: 19.53\\n JV default FF: 0.41\\n JV default PCE: 7.82@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: ALD | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 14.44\\n JV default FF: 0.43\\n JV default PCE: 5.61@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: ALD | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.83\\n JV default Jsc: 12.07\\n JV default FF: 0.32\\n JV default PCE: 3.21@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: ALD | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Doctor blading\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.84\\n JV default Jsc: 11.57\\n JV default FF: 0.36\\n JV default PCE: 3.54@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbBr0.15I2.85\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 14.70\\n JV default FF: 0.60\\n JV default PCE: 9.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbBr0.15I2.85\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 15.60\\n JV default FF: 0.40\\n JV default PCE: 7.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbBr0.15I2.85\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.60\\n JV default Jsc: 9.50\\n JV default FF: 0.20\\n JV default PCE: 1.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbBr0.15I2.85\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 9.90\\n JV default FF: 0.70\\n JV default PCE: 7.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 120\\n Perovskite deposition thermal annealing time: Unknown >> 20.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: Cu\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.03\\n JV default Jsc: 21.11\\n JV default FF: 0.78\\n JV default PCE: 17.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown >> 120\\n Perovskite deposition thermal annealing time: Unknown >> 20.0\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 20.24\\n JV default FF: 0.71\\n JV default PCE: 13.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: CeOx\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: Unknown >> 150\\n Perovskite deposition thermal annealing time: Unknown >> 120.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 21.44\\n JV default FF: 0.62\\n JV default PCE: 16.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: Unknown >> 150\\n Perovskite deposition thermal annealing time: Unknown >> 120.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.91\\n JV default Jsc: 20.32\\n JV default FF: 0.54\\n JV default PCE: 16.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: Unknown >> 150\\n Perovskite deposition thermal annealing time: Unknown >> 120.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 21.62\\n JV default FF: 0.69\\n JV default PCE: 16.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: CeOx | PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: Unknown >> 150\\n Perovskite deposition thermal annealing time: Unknown >> 120.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 22.90\\n JV default FF: 0.70\\n JV default PCE: 16.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 17.39\\n JV default FF: 0.69\\n JV default PCE: 12.23@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 17.60\\n JV default FF: 0.71\\n JV default PCE: 12.74@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 17.30\\n JV default FF: 0.73\\n JV default PCE: 12.67@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 17.41\\n JV default FF: 0.69\\n JV default PCE: 12.38@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 17.72\\n JV default FF: 0.70\\n JV default PCE: 12.62@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 17.83\\n JV default FF: 0.71\\n JV default PCE: 12.84@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 17.35\\n JV default FF: 0.73\\n JV default PCE: 12.56@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 17.31\\n JV default FF: 0.67\\n JV default PCE: 11.78@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 17.45\\n JV default FF: 0.72\\n JV default PCE: 12.58@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 17.42\\n JV default FF: 0.72\\n JV default PCE: 12.51@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 17.70\\n JV default FF: 0.72\\n JV default PCE: 12.78@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD | MoOx\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating | Evaporation\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 17.79\\n JV default FF: 0.71\\n JV default PCE: 12.76@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 18.75\\n JV default FF: 0.64\\n JV default PCE: 11.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.97\\n JV default Jsc: 21.57\\n JV default FF: 0.62\\n JV default PCE: 12.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c | C60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 19.20\\n JV default FF: 0.71\\n JV default PCE: 14.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 21.93\\n JV default FF: 0.49\\n JV default PCE: 9.70@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 22.20\\n JV default FF: 0.54\\n JV default PCE: 10.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.89\\n JV default Jsc: 17.16\\n JV default FF: 0.42\\n JV default PCE: 6.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 21.80\\n JV default FF: 0.51\\n JV default PCE: 10.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 22.09\\n JV default FF: 0.57\\n JV default PCE: 12.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 22.47\\n JV default FF: 0.54\\n JV default PCE: 11.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: ZnO-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 50\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 21.84\\n JV default FF: 0.55\\n JV default PCE: 11.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: AsI3 | NH4Cl\\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 5.15\\n JV default FF: 0.49\\n JV default PCE: 2.19@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: AsI3 | NH4Cl\\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.85\\n JV default Jsc: 3.68\\n JV default FF: 0.43\\n JV default PCE: 1.35@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: AsI3 | NH4Cl\\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.76\\n JV default Jsc: 13.50\\n JV default FF: 0.62\\n JV default PCE: 6.37@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: AsI3 | NH4Cl\\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.75\\n JV default Jsc: 12.80\\n JV default FF: 0.55\\n JV default PCE: 5.26@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Carbon\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Electrospinning\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 19.00\\n JV default FF: 0.70\\n JV default PCE: 13.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.86\\n JV default Jsc: 16.72\\n JV default FF: 0.66\\n JV default PCE: 9.55@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 16.88\\n JV default FF: 0.66\\n JV default PCE: 9.62@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 18.71\\n JV default FF: 0.65\\n JV default PCE: 10.78@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 19.14\\n JV default FF: 0.69\\n JV default PCE: 12.17@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 18.19\\n JV default FF: 0.66\\n JV default PCE: 11.29@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 17.97\\n JV default FF: 0.66\\n JV default PCE: 10.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: Bi2S3\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 18.60\\n JV default FF: 0.74\\n JV default PCE: 13.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.67\\n JV default Jsc: 8.33\\n JV default FF: 0.55\\n JV default PCE: 3.04@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | TiCl4\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PbS-QDs\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.47\\n JV default Jsc: 8.60\\n JV default FF: 0.50\\n JV default PCE: 2.06@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | TiCl4\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PbS-QDs\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.34\\n JV default Jsc: 24.63\\n JV default FF: 0.43\\n JV default PCE: 3.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown | TiCl4\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 15\\n HTL stack sequence: PbS-QDs\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.59\\n JV default Jsc: 11.00\\n JV default FF: 0.47\\n JV default PCE: 2.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.21\\n JV default Jsc: 0.08\\n JV default FF: 0.29\\n JV default PCE: 0.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> DMF; IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 15.86\\n JV default FF: 0.67\\n JV default PCE: 9.91@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 12.38\\n JV default FF: 0.42\\n JV default PCE: 4.48@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> DMF; IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 15.41\\n JV default FF: 0.49\\n JV default PCE: 6.63@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> DMF; IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.85\\n JV default Jsc: 15.30\\n JV default FF: 0.48\\n JV default PCE: 6.23@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 15.09\\n JV default FF: 0.50\\n JV default PCE: 6.81@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> DMF; IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 16.10\\n JV default FF: 0.65\\n JV default PCE: 9.65@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> DMF; IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 14.57\\n JV default FF: 0.63\\n JV default PCE: 8.45@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.91\\n JV default Jsc: 14.71\\n JV default FF: 0.55\\n JV default PCE: 7.28@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> DMF; IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 16.09\\n JV default FF: 0.59\\n JV default PCE: 8.84@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> DMF; IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 100.0\\n Perovskite deposition thermal annealing time: 3.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.87\\n JV default Jsc: 13.30\\n JV default FF: 0.48\\n JV default PCE: 5.57@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 60.0; 100.0\\n Perovskite deposition thermal annealing time: 5.0; 10.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Evaporation\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 18.92\\n JV default FF: 0.61\\n JV default PCE: 10.32@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 60.0; 100.0\\n Perovskite deposition thermal annealing time: 5.0; 10.0\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Evaporation\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 21.29\\n JV default FF: 0.72\\n JV default PCE: 16.79@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 5\\n HTL stack sequence: CuOx\\n HTL additives compounds: \\n HTL deposition procedure: Evaporation\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 13.88\\n JV default FF: 0.56\\n JV default PCE: 7.32@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 5\\n HTL stack sequence: CuOx\\n HTL additives compounds: \\n HTL deposition procedure: Evaporation\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96\\n JV default Jsc: 14.40\\n JV default FF: 0.59\\n JV default PCE: 8.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMSO; GBL\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 5\\n HTL stack sequence: CuOx\\n HTL additives compounds: \\n HTL deposition procedure: Evaporation\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 10.28\\n JV default FF: 0.54\\n JV default PCE: 5.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 21.95\\n JV default FF: 0.74\\n JV default PCE: 17.87@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 17.04\\n JV default FF: 0.69\\n JV default PCE: 12.72@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMF; DMSO >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: 50.0; 100 >> 150.0\\n Perovskite deposition thermal annealing time: 5.0; 10.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.22\\n JV default Jsc: 10.30\\n JV default FF: 0.45\\n JV default PCE: 0.97@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMF; DMSO >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: 50.0; 100 >> 150.0\\n Perovskite deposition thermal annealing time: 5.0; 10.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.26\\n JV default Jsc: 12.40\\n JV default FF: 0.45\\n JV default PCE: 1.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMF; DMSO >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: 50.0; 100 >> 150.0\\n Perovskite deposition thermal annealing time: 5.0; 10.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.27\\n JV default Jsc: 17.26\\n JV default FF: 0.48\\n JV default PCE: 2.23@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMF; DMSO >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: 50.0; 100 >> 150.0\\n Perovskite deposition thermal annealing time: 5.0; 10.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.21\\n JV default Jsc: 12.50\\n JV default FF: 0.46\\n JV default PCE: 1.18@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: CsSnI3\\n Perovskite composition short form: CsSnI\\n Perovskite additives compounds: SnF2\\n Perovskite deposition solvents: DMF; DMSO >> none\\n Perovskite deposition procedure: Spin-coating >> Evaporation\\n Perovskite deposition thermal annealing temperature: 50.0; 100 >> 150.0\\n Perovskite deposition thermal annealing time: 5.0; 10.0 >> 10.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.11\\n JV default Jsc: 10.50\\n JV default FF: 0.30\\n JV default PCE: 0.37@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 20.80\\n JV default FF: 0.64\\n JV default PCE: 13.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ1; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.07\\n JV default Jsc: 22.00\\n JV default FF: 0.65\\n JV default PCE: 15.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ1; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 22.50\\n JV default FF: 0.73\\n JV default PCE: 18.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ1; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.12\\n JV default Jsc: 22.80\\n JV default FF: 0.73\\n JV default PCE: 18.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ1; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.12\\n JV default Jsc: 22.80\\n JV default FF: 0.75\\n JV default PCE: 19.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ1; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 22.80\\n JV default FF: 0.75\\n JV default PCE: 19.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Al2O3 | Spiro-MeOTAD\\n HTL additives compounds: Unknown | JQ1; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.12\\n JV default Jsc: 23.20\\n JV default FF: 0.73\\n JV default PCE: 18.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ1; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09\\n JV default Jsc: 22.60\\n JV default FF: 0.74\\n JV default PCE: 18.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ2; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.07\\n JV default Jsc: 22.50\\n JV default FF: 0.64\\n JV default PCE: 15.70@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ2; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 21.80\\n JV default FF: 0.68\\n JV default PCE: 15.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ3; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09\\n JV default Jsc: 21.90\\n JV default FF: 0.72\\n JV default PCE: 17.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ3; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09\\n JV default Jsc: 21.90\\n JV default FF: 0.73\\n JV default PCE: 18.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: JQ3; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 21.80\\n JV default FF: 0.66\\n JV default PCE: 15.50@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09\\n JV default Jsc: 22.00\\n JV default FF: 0.74\\n JV default PCE: 18.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 20.40\\n JV default FF: 0.70\\n JV default PCE: 15.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 19.92\\n JV default FF: 0.61\\n JV default PCE: 12.10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl | ZnCl2\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 20.61\\n JV default FF: 0.67\\n JV default PCE: 14.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl | ZnCl2\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 21.98\\n JV default FF: 0.70\\n JV default PCE: 16.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl | ZnCl2\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 20.86\\n JV default FF: 0.63\\n JV default PCE: 13.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl | ZnCl2\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 19.64\\n JV default FF: 0.58\\n JV default PCE: 10.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl | ZnCl2\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.85\\n JV default Jsc: 18.37\\n JV default FF: 0.56\\n JV default PCE: 8.70@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 30.0 >> 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 10.61\\n JV default FF: 0.42\\n JV default PCE: 4.44@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 30.0 >> 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 20.47\\n JV default FF: 0.70\\n JV default PCE: 14.41@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: In2O3 | PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 30.0 >> 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05\\n JV default Jsc: 16.88\\n JV default FF: 0.63\\n JV default PCE: 11.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: In2O3 | PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 30.0 >> 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.07\\n JV default Jsc: 17.90\\n JV default FF: 0.68\\n JV default PCE: 13.01@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: In2O3 | PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 30.0 >> 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99\\n JV default Jsc: 17.56\\n JV default FF: 0.61\\n JV default PCE: 10.54@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: In2O3 | PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 30.0 >> 40.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 16.21\\n JV default FF: 0.50\\n JV default PCE: 7.88@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 21.00\\n JV default FF: 0.67\\n JV default PCE: 14.99@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | ZnSe\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 21.01\\n JV default FF: 0.70\\n JV default PCE: 15.62@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | ZnSe\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 22.50\\n JV default FF: 0.70\\n JV default PCE: 16.96@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | ZnSe\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.10\\n JV default Jsc: 22.18\\n JV default FF: 0.75\\n JV default PCE: 18.38@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | ZnSe\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 23.38\\n JV default FF: 0.72\\n JV default PCE: 18.15@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | ZnSe\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 21.39\\n JV default FF: 0.68\\n JV default PCE: 14.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: PTAA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05\\n JV default Jsc: 23.35\\n JV default FF: 0.76\\n JV default PCE: 18.53@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | ZnSe\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: FA0.9MA0.1PbBr0.3I2.7\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96\\n JV default Jsc: 21.57\\n JV default FF: 0.75\\n JV default PCE: 15.55@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Glycine\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 10.0 >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 16.20\\n JV default FF: 0.60\\n JV default PCE: 9.48@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> CBD\\n Perovskite deposition thermal annealing temperature: 70.0 >> 70.0\\n Perovskite deposition thermal annealing time: 10.0 >> 30.0\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 12.56\\n JV default FF: 0.58\\n JV default PCE: 6.99@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.07\\n JV default Jsc: 21.13\\n JV default FF: 0.78\\n JV default PCE: 17.52@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.08\\n JV default Jsc: 21.18\\n JV default FF: 0.78\\n JV default PCE: 17.81@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09\\n JV default Jsc: 21.25\\n JV default FF: 0.79\\n JV default PCE: 18.21@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09\\n JV default Jsc: 21.22\\n JV default FF: 0.79\\n JV default PCE: 18.19@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 20.72\\n JV default FF: 0.72\\n JV default PCE: 15.62@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.04\\n JV default Jsc: 20.83\\n JV default FF: 0.73\\n JV default PCE: 15.84@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05\\n JV default Jsc: 20.90\\n JV default FF: 0.73\\n JV default PCE: 16.08@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05\\n JV default Jsc: 20.81\\n JV default FF: 0.73\\n JV default PCE: 15.93@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.00\\n JV default Jsc: 18.91\\n JV default FF: 0.70\\n JV default PCE: 13.25@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 18.59\\n JV default FF: 0.71\\n JV default PCE: 13.27@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 18.82\\n JV default FF: 0.71\\n JV default PCE: 13.42@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: PET | ITO\\n ETL stack sequence: c-HATNA | bis-C60\\n ETL additives compounds: Triethylamine | Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: c-TCTA\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 18.51\\n JV default FF: 0.70\\n JV default PCE: 13.31@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Unknown\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 19.00\\n JV default FF: 0.70\\n JV default PCE: 10.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.03\\n JV default Jsc: 21.60\\n JV default FF: 0.72\\n JV default PCE: 15.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05\\n JV default Jsc: 20.00\\n JV default FF: 0.72\\n JV default PCE: 15.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.97\\n JV default Jsc: 21.10\\n JV default FF: 0.59\\n JV default PCE: 12.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 90\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96\\n JV default Jsc: 15.40\\n JV default FF: 0.56\\n JV default PCE: 8.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2-np\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: acetonitrile\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: none\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Unknown\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.95\\n JV default Jsc: 22.30\\n JV default FF: 0.50\\n JV default PCE: 10.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: SnO2\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: acetonitrile\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.06\\n JV default Jsc: 21.68\\n JV default FF: 0.76\\n JV default PCE: 17.51@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: none\\n Perovskite deposition procedure: Co-evaporation\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.77\\n JV default Jsc: 9.46\\n JV default FF: 0.69\\n JV default PCE: 5.03@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: none\\n Perovskite deposition procedure: Co-evaporation\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.77\\n JV default Jsc: 13.98\\n JV default FF: 0.68\\n JV default PCE: 7.27@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: none\\n Perovskite deposition procedure: Co-evaporation\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.79\\n JV default Jsc: 12.27\\n JV default FF: 0.65\\n JV default PCE: 6.29@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | Bphen\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: none\\n Perovskite deposition procedure: Co-evaporation\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: none\\n HTL additives compounds: \\n HTL deposition procedure: Unknown\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.69\\n JV default Jsc: 10.79\\n JV default FF: 0.63\\n JV default PCE: 4.65@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 120\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.93\\n JV default Jsc: 20.41\\n JV default FF: 0.72\\n JV default PCE: 13.58@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: Unknown\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 120\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.91\\n JV default Jsc: 19.37\\n JV default FF: 0.71\\n JV default PCE: 12.59@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 17.27\\n JV default FF: 0.60\\n JV default PCE: 9.40@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.70\\n JV default Jsc: 7.48\\n JV default FF: 0.37\\n JV default PCE: 1.86@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 30\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.94\\n JV default Jsc: 20.36\\n JV default FF: 0.57\\n JV default PCE: 10.78@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.68\\n JV default Jsc: 11.31\\n JV default FF: 0.41\\n JV default PCE: 3.08@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 60\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.82\\n JV default Jsc: 10.60\\n JV default FF: 0.47\\n JV default PCE: 4.32@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 110\\n Perovskite deposition thermal annealing time: 80\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.78\\n JV default Jsc: 13.86\\n JV default FF: 0.55\\n JV default PCE: 5.83@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 17.47\\n JV default FF: 0.72\\n JV default PCE: 12.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 14.20\\n JV default FF: 0.77\\n JV default PCE: 10.00@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 10\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 11.94\\n JV default FF: 0.78\\n JV default PCE: 8.20@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: FA0.85MA0.15PbBr0.45I2.55\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150\\n Perovskite deposition thermal annealing time: 6\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: Graphene Oxide\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.90\\n JV default Jsc: 18.72\\n JV default FF: 0.75\\n JV default PCE: 12.68@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: TPE-2\\n7-Carbazole W1\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01\\n JV default Jsc: 21.55\\n JV default FF: 0.69\\n JV default PCE: 14.92@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: TPE-2\\n7-Carbazole W2\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.02\\n JV default Jsc: 22.23\\n JV default FF: 0.74\\n JV default PCE: 16.74@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation\\n Perovskite composition long form: FA0.85MA0.15PbBr0.45I2.55\\n Perovskite composition short form: FAMAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 150\\n Perovskite deposition thermal annealing time: 6\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: Graphene Oxide\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 16.57\\n JV default FF: 0.68\\n JV default PCE: 10.39@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: TPE-2\\n7-Carbazole W4\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98\\n JV default Jsc: 19.76\\n JV default FF: 0.69\\n JV default PCE: 13.30@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: Cl\\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 95\\n Perovskite deposition thermal annealing time: 40\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Ag\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.03\\n JV default Jsc: 20.58\\n JV default FF: 0.71\\n JV default PCE: 15.01@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: Cs3Sb2I9\\n Perovskite composition short form: CsSbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.40\\n JV default Jsc: 0.13\\n JV default FF: 0.58\\n JV default PCE: 0.03@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: Rb3Sb2I9\\n Perovskite composition short form: RbSbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.66\\n JV default Jsc: 1.84\\n JV default FF: 0.63\\n JV default PCE: 0.76@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | FTO\\n ETL stack sequence: TiO2-c | TiO2-mp\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spray-pyrolys | Spin-coating\\n Perovskite composition long form: K3Sb2I9\\n Perovskite composition short form: KSbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF; DMSO\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: 100\\n Perovskite deposition thermal annealing time: 20\\n HTL stack sequence: Spiro-MeOTAD\\n HTL additives compounds: FK209; Li-TFSI; TBP\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Au\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: nip\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.34\\n JV default Jsc: 0.41\\n JV default FF: 0.50\\n JV default PCE: 0.07@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: PEDOT:PSS\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.62\\n JV default Jsc: 9.39\\n JV default FF: 0.66\\n JV default PCE: 3.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.92\\n JV default Jsc: 12.43\\n JV default FF: 0.68\\n JV default PCE: 7.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88\\n JV default Jsc: 13.53\\n JV default FF: 0.58\\n JV default PCE: 6.90@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.72\\n JV default Jsc: 10.71\\n JV default FF: 0.59\\n JV default PCE: 4.60@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.76\\n JV default Jsc: 9.51\\n JV default FF: 0.66\\n JV default PCE: 4.80@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Evaporation | Evaporation\\n Perovskite composition long form: MAPbI3\\n Perovskite composition short form: MAPbI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF\\n Perovskite deposition procedure: Spin-coating\\n Perovskite deposition thermal annealing temperature: Unknown\\n Perovskite deposition thermal annealing time: Unknown\\n HTL stack sequence: NiO-c\\n HTL additives compounds: \\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.74\\n JV default Jsc: 12.95\\n JV default FF: 0.60\\n JV default PCE: 5.70@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \" Substrate stack sequence: SLG | ITO\\n ETL stack sequence: PCBM-60 | C60 | BCP\\n ETL additives compounds: Unknown\\n ETL deposition procedure: Spin-coating | Evaporation | Evaporation\\n Perovskite composition long form: MAPbBr0.5I2.5\\n Perovskite composition short form: MAPbBrI\\n Perovskite additives compounds: \\n Perovskite deposition solvents: DMF >> IPA\\n Perovskite deposition procedure: Spin-coating >> Spin-coating\\n Perovskite deposition thermal annealing temperature: 100.0 >> 75.0; 100\\n Perovskite deposition thermal annealing time: 5.0 >> 15.0; 75.0\\n HTL stack sequence: PTAA\\n HTL additives compounds: F4-TCNQ\\n HTL deposition procedure: Spin-coating\\n Backcontact stack sequence: Al\\n Backcontact additives compounds: \\n Backcontact deposition procedure: Evaporation\\n Cell architecture: pin\\n Cell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.16\\n JV default Jsc: 18.30\\n JV default FF: 0.78\\n JV default PCE: 16.60@@@\"}]"
  },
  {
    "path": "SII_MDP/data/regression40.json",
    "content": "[{\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: PCBM-60 | C60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Evaporation | Evaporation \\nPerovskite composition long form: MAPbBr0.8I2.2 \\nPerovskite composition short form: MAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> Spin-coating \\nPerovskite deposition thermal annealing temperature: 100.0 >> 75.0; 100 \\nPerovskite deposition thermal annealing time: 5.0 >> 15.0; 75.0 \\nHTL stack sequence: PTAA \\nHTL additives compounds: F4-TCNQ \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Al \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.21 \\n JV default Jsc: 15.8 \\n JV default FF: 0.779 \\n JV default PCE: 14.9@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: PCBM-60 \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: Cs0.05FA0.83MA0.17PbBr0.17I0.83 \\nPerovskite composition short form: CsFAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF; DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 150 \\nPerovskite deposition thermal annealing time: 30 \\nHTL stack sequence: NiO-np \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.071 \\n JV default Jsc: 19.15 \\n JV default FF: 0.65 \\n JV default PCE: 13.26@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: C60; PCBM-60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: Cs0.05FA0.83MA0.17PbBr0.17I0.83 \\nPerovskite composition short form: CsFAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF; DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 150 \\nPerovskite deposition thermal annealing time: 30 \\nHTL stack sequence: NiO-np \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.043 \\n JV default Jsc: 21.13 \\n JV default FF: 0.62 \\n JV default PCE: 13.57@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: C60; PCBM-60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: Cs0.05FA0.83MA0.17PbBr0.17I0.83 \\nPerovskite composition short form: CsFAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF; DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 150 \\nPerovskite deposition thermal annealing time: 30 \\nHTL stack sequence: NiO-np \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.986 \\n JV default Jsc: 21.56 \\n JV default FF: 0.69 \\n JV default PCE: 14.61@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: C60; PCBM-60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: Cs0.05FA0.83MA0.17PbBr0.17I0.83 \\nPerovskite composition short form: CsFAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF; DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 150 \\nPerovskite deposition thermal annealing time: 30 \\nHTL stack sequence: NiO-np \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.043 \\n JV default Jsc: 22.67 \\n JV default FF: 0.682 \\n JV default PCE: 16.12@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: Cs0.05FA0.83MA0.17PbBr0.17I0.83 \\nPerovskite composition short form: CsFAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF; DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 150 \\nPerovskite deposition thermal annealing time: 30 \\nHTL stack sequence: NiO-np \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.9 \\n JV default Jsc: 21.62 \\n JV default FF: 0.61 \\n JV default PCE: 11.92@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.835 \\n JV default Jsc: 16.91 \\n JV default FF: 0.58 \\n JV default PCE: 8.23@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.845 \\n JV default Jsc: 18.55 \\n JV default FF: 0.58 \\n JV default PCE: 9.12@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.833 \\n JV default Jsc: 19.31 \\n JV default FF: 0.595 \\n JV default PCE: 9.57@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.829 \\n JV default Jsc: 19.48 \\n JV default FF: 0.625 \\n JV default PCE: 10.09@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.813 \\n JV default Jsc: 5.55 \\n JV default FF: 0.413 \\n JV default PCE: 1.86@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.004 \\n JV default Jsc: 17.9 \\n JV default FF: 0.607 \\n JV default PCE: 10.91@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.016 \\n JV default Jsc: 20.85 \\n JV default FF: 0.566 \\n JV default PCE: 11.99@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: DMF \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.023 \\n JV default Jsc: 20.36 \\n JV default FF: 0.581 \\n JV default PCE: 12.1@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: PCBM-60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: FA0.85MA0.15PbBr0.45I2.55 \\nPerovskite composition short form: FAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: PEDOT:PSS \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1 \\n JV default Jsc: 21.25 \\n JV default FF: 0.772 \\n JV default PCE: 16.4@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: PCBM-60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: FA0.85MA0.15PbBr0.45I2.55 \\nPerovskite composition short form: FAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: P8TTT \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.97 \\n JV default Jsc: 14.08 \\n JV default FF: 0.583 \\n JV default PCE: 7.96@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: PCBM-60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: FA0.85MA0.15PbBr0.45I2.55 \\nPerovskite composition short form: FAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: PII2T8T \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.09 \\n JV default Jsc: 21.48 \\n JV default FF: 0.778 \\n JV default PCE: 18.22@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | ITO \\nETL stack sequence: PCBM-60 | BCP \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: FA0.85MA0.15PbBr0.45I2.55 \\nPerovskite composition short form: FAMAPbBrI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 100 \\nPerovskite deposition thermal annealing time: 45 \\nHTL stack sequence: PII2T8TSi \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Ag \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: pin \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.05 \\n JV default Jsc: 18.42 \\n JV default FF: 0.759 \\n JV default PCE: 14.61@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: none \\nHTL additives compounds: \\nHTL deposition procedure: Unknown \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.516 \\n JV default Jsc: 9.45 \\n JV default FF: 0.283 \\n JV default PCE: 1.38@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: ZnPc(tBu)4 \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.783 \\n JV default Jsc: 11.67 \\n JV default FF: 0.357 \\n JV default PCE: 3.26@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: ZnPc(tBu)4 \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.786 \\n JV default Jsc: 14.42 \\n JV default FF: 0.356 \\n JV default PCE: 4.04@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: ZnPc(tBu)4 \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.918 \\n JV default Jsc: 16.29 \\n JV default FF: 0.533 \\n JV default PCE: 7.98@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: ZnPc(tBu)4 \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.825 \\n JV default Jsc: 16.28 \\n JV default FF: 0.383 \\n JV default PCE: 5.15@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: ZnPc(tBu)4 \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.898 \\n JV default Jsc: 11.58 \\n JV default FF: 0.354 \\n JV default PCE: 3.68@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.895 \\n JV default Jsc: 16.61 \\n JV default FF: 0.416 \\n JV default PCE: 6.19@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMF >> IPA \\nPerovskite deposition procedure: Spin-coating >> CBD \\nPerovskite deposition thermal annealing temperature: 90.0 >> 70.0 \\nPerovskite deposition thermal annealing time: 5.0 >> 30.0 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.934 \\n JV default Jsc: 20.48 \\n JV default FF: 0.569 \\n JV default PCE: 10.88@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Hot-casting \\nPerovskite deposition thermal annealing temperature: 130 \\nPerovskite deposition thermal annealing time: 60 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.888 \\n JV default Jsc: 23.908 \\n JV default FF: 0.667 \\n JV default PCE: 14.16@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-nt \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Hot-casting \\nPerovskite deposition thermal annealing temperature: 130 \\nPerovskite deposition thermal annealing time: 60 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.888 \\n JV default Jsc: 24.705 \\n JV default FF: 0.66 \\n JV default PCE: 14.49@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-nt \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Hot-casting \\nPerovskite deposition thermal annealing temperature: 130 \\nPerovskite deposition thermal annealing time: 60 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.884 \\n JV default Jsc: 25.307 \\n JV default FF: 0.663 \\n JV default PCE: 14.83@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-nt \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Hot-casting \\nPerovskite deposition thermal annealing temperature: 130 \\nPerovskite deposition thermal annealing time: 60 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.886 \\n JV default Jsc: 25.5 \\n JV default FF: 0.679 \\n JV default PCE: 15.34@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-nt \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Hot-casting \\nPerovskite deposition thermal annealing temperature: 130 \\nPerovskite deposition thermal annealing time: 60 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.863 \\n JV default Jsc: 25.888 \\n JV default FF: 0.657 \\n JV default PCE: 14.68@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-nt \\nETL additives compounds: Unknown \\nETL deposition procedure: Spin-coating | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: Cl \\nPerovskite deposition solvents: Unknown \\nPerovskite deposition procedure: Hot-casting \\nPerovskite deposition thermal annealing temperature: 130 \\nPerovskite deposition thermal annealing time: 60 \\nHTL stack sequence: Spiro-MeOTAD \\nHTL additives compounds: Li-TFSI; TBP \\nHTL deposition procedure: Spin-coating \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.865 \\n JV default Jsc: 25.223 \\n JV default FF: 0.64 \\n JV default PCE: 13.96@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96 \\n JV default Jsc: 18 \\n JV default FF: 0.35 \\n JV default PCE: 6.1@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.96 \\n JV default Jsc: 17.6 \\n JV default FF: 0.39 \\n JV default PCE: 6.6@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.97 \\n JV default Jsc: 18 \\n JV default FF: 0.44 \\n JV default PCE: 8@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.97 \\n JV default Jsc: 19.1 \\n JV default FF: 0.51 \\n JV default PCE: 9.4@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 1.01 \\n JV default Jsc: 18.8 \\n JV default FF: 0.51 \\n JV default PCE: 9.7@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.99 \\n JV default Jsc: 18.8 \\n JV default FF: 0.55 \\n JV default PCE: 10@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.98 \\n JV default Jsc: 19.1 \\n JV default FF: 0.51 \\n JV default PCE: 9.6@@@\"}, {\"instruction\": \"What's the PCE of the perovskite solar cell with the parameters below.\", \"input\": \"Substrate stack sequence: SLG | FTO \\nETL stack sequence: TiO2-c | TiO2-mp \\nETL additives compounds: Unknown \\nETL deposition procedure: Spray-pyrolys | Spin-coating \\nPerovskite composition long form: MAPbI3 \\nPerovskite composition short form: MAPbI \\nPerovskite additives compounds: \\nPerovskite deposition solvents: DMSO \\nPerovskite deposition procedure: Spin-coating \\nPerovskite deposition thermal annealing temperature: 120 \\nPerovskite deposition thermal annealing time: 10 \\nHTL stack sequence: C5PcH2 | MoOx \\nHTL additives compounds: \\nHTL deposition procedure: Spin-coating | Evaporation \\nBackcontact stack sequence: Au \\nBackcontact additives compounds: \\nBackcontact deposition procedure: Evaporation \\nCell architecture: nip \\nCell semitransparent: FALSE###\", \"output\": \" JV default Voc: 0.88 \\n JV default Jsc: 17.7 \\n JV default FF: 0.45 \\n JV default PCE: 7@@@\"}]"
  },
  {
    "path": "SII_MDP/data/sii360.json",
    "content": "[{\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The following chemicals were obtained from commercial suppliers and used as received: PbI2 (99%, Sigma\\u2013Aldrich), MAI (>98%, Tokyo Chemical Industry Co., Japan), PCBM (99.5%, Lumtec Co., Taiwan), bathocuproine (Wako), Graphene oxide (2\\u202fmg\\u202fmL\\u22121, Sigma-Aldrich), Super dehydrated dimethylsulfoxide (DMSO), gamma-Butyrolactone (GBL), toluene, and methanol were purchased from Wako, Japan. All the chemicals were used as received without further purification.\\n\\nThe r-GO film was prepared on top of the ITO glass from a 0.5\\u202fmg\\u202fmL-1 aqueous solution and annealed at 150\\u202f\\u00b0C for 90\\u202fmin to form a 2.5\\u202fnm thick r-GO film. After cooling down the r-GO films to room temperature, a 10\\u202fnm uniform CuSCN layer (from a solution of 10\\u202fmg\\u202fmL-1 in diethyl sulfide) was obtained by spin-coating at 6000\\u202frpm for 60\\u202fs on top of it and was annealed for 30\\u202fmin in air. The thickness of the CuSCN layer between 10\\u202fnm and 40\\u202fnm was obtained by controlling the rotation speed of the spin coater between 3000 and 6000\\u202frpm (see Table S2). Then the r-GO/CuSCN coated ITO glasses were cooled down to room temperature and transferred to a N2 glovebox. A MAPbI3 precursor solution (100\\u202f\\u03bcL) consisting of PbI2 (922\\u202fmg) and CH3NH3I (318\\u202fmg) dissolved in 2\\u202fmL of 3:7 (v/v) DMSO/GBL was spread over the r-GO/CuSCN film and spin-coated with two steps of spin-coating, first at 1000\\u202frpm for 12\\u202fs and then 5000\\u202frpm for 30\\u202fs. 100\\u202f\\u03bcL of toluene was dropped onto the perovskite-coated r-GO/CuSCN film 10\\u202fs prior to the start of second stage of spin-coating at 5000\\u202frpm. Finally, the film was annealed at 100\\u202f\\u00b0C for 30\\u202fmin resulting in a 400\\u202fnm thick MAPbI3 layer. All the MAPbI3 layers has been fabricated with similar thickness regardless in the thickness variation of HTL layers. After cooling down to room temperature, a solution of PCBM in chlorobenzene (20\\u202fmg\\u202fmL\\u22121) was spin-coated on top of the film at a rotation speed of 1000\\u202frpm for 30\\u202fs. A saturated methanol solution of bathocuproine (140\\u202f\\u03bcL) was spin-coated onto the PCBM coated film with spin rotation of 6000\\u202frpm for 30\\u202fs. The PSC fabrication was completed by thermal evaporation of a 100\\u202fnm thick film of Ag as the cathode.\\nSupplementary data associated with this article can be found, in the online version, at https://doi.org/10.1016/j.solener.2018.07.022.\\nThe r-GO film was prepared on top of the ITO glass from a 0.5\\u202fmg\\u202fmL-1 aqueous solution and annealed at 150\\u202f\\u00b0C for 90\\u202fmin to form a 2.5\\u202fnm thick r-GO film. After cooling down the r-GO films to room temperature, a 10\\u202fnm uniform CuSCN layer (from a solution of 10\\u202fmg\\u202fmL-1 in diethyl sulfide) was obtained by spin-coating at 6000\\u202frpm for 60\\u202fs on top of it and was annealed for 30\\u202fmin in air. The thickness of the CuSCN layer between 10\\u202fnm and 40\\u202fnm was obtained by controlling the rotation speed of the spin coater between 3000 and 6000\\u202frpm (see Table S2 ). Then the r-GO/CuSCN coated ITO glasses were cooled down to room temperature and transferred to a N2 glovebox. A MAPbI3 precursor solution (100\\u202f\\u03bcL) consisting of PbI2 (922\\u202fmg) and CH3NH3I (318\\u202fmg) dissolved in 2\\u202fmL of 3:7 (v/v) DMSO/GBL was spread over the r-GO/CuSCN film and spin-coated with two steps of spin-coating, first at 1000\\u202frpm for 12\\u202fs and then 5000\\u202frpm for 30\\u202fs. 100\\u202f\\u03bcL of toluene was dropped onto the perovskite-coated r-GO/CuSCN film 10\\u202fs prior to the start of second stage of spin-coating at 5000\\u202frpm. Finally, the film was annealed at 100\\u202f\\u00b0C for 30\\u202fmin resulting in a 400\\u202fnm thick MAPbI3 layer. All the MAPbI3 layers has been fabricated with similar thickness regardless in the thickness variation of HTL layers. After cooling down to room temperature, a solution of PCBM in chlorobenzene (20\\u202fmg\\u202fmL\\u22121) was spin-coated on top of the film at a rotation speed of 1000\\u202frpm for 30\\u202fs. A saturated methanol solution of bathocuproine (140\\u202f\\u03bcL) was spin-coated onto the PCBM coated film with spin rotation of 6000\\u202frpm for 30\\u202fs. The PSC fabrication was completed by thermal evaporation of a 100\\u202fnm thick film of Ag as the cathode.\\n\\nThe thickness of the fabricated r-GO, CuSCN and r-GO/CuSCN films were measured with J.A. Woollam (M-2000X) elipsometer. The angel of incident light was set at 45\\u00b0 for reflectance measurement of thickness of all the films. FESEM images were obtained with a Hitachi S-4800 field emission scanning electron microscope. The atomic force microscopy images were obtained with JSPM-5200 scanning probe microscope. UV\\u2013Vis spectra were measured on a Shimadzu UV\\u2013Vis 3600 spectrophotometer. Steady-state PL spectra were measured with an Edinburgh FLS 920 fluorescence spectrometer (Edinburgh). XRD patterns were collected on a Rigaku RINT-2500 powder X-ray diffractometer equipped with a Cu K\\u03b1 radiation source. The energies of the highest occupied molecular orbitals of the films were estimated by photoelectron yield spectroscopy with an AC-3e spectrometer (Riken Keiki). Current\\u2013voltage (J-V) characteristics were measured by means of AM 1.5 illumination at 100\\u202fmW\\u202fcm\\u22122 with a solar simulator (WXS-155S-10, Wacom Denso) under ambient conditions with a delay time of 100\\u202fms. J\\u2013V curves for all devices were measured by masking the devices with a metal mask with an area of 1.02\\u202fcm2. Monochromatic incident photon-to-current conversion efficiency spectra were measured with monochromatic incident light (1\\u202f\\u00d7\\u202f1016\\u202fphotons\\u202fcm\\u22122) in direct-current mode (CEP-2000BX, Bunko- Keiki). The light intensity of the solar simulator was calibrated with a standard silicon solar cell (PV Measurements). Light-soaking stability was tested on a solar cell light resistance test system (BIR-50, Bunko- Keiki), and a Keithley was used for automatically recording J\\u2013V curves.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: rGO | CuSCN,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 100,\\n Stability_PCE_initial_value: 14.1,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 1.02,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned fluorine-doped tin oxide (FTO) glass substrates were obtained through etching using zinc powder and hydrochloride acid. Formamidinium iodide (FAI, 99% purity) was purchased from Shanghai Materwin. Spiro-OMeTAD (2,2\\u2032,7,7\\u2032-tetrakis(N,N-dip-methoxyphenylamine)-9,9\\u2032-spirobifluorene, 99% purity) was bought from Merck. Other materials, including titanium diisopropoxide bis(acetylacetonate) (TDBA, 99.8% purity), lead(II) iodide (PbI2, 99%), 4-tert-butylpyridine (tBP, 99% purity), lithium\\u2013bis(trifluoromethanesulfonyl)imide (Li\\u2013TFSI, 99% purity) and thiocyanate ammonium (NH4SCN, 99.99% purity), were supplied by Sigma-Aldrich. All materials are used without further purification.\\n\\nA patterned FTO glass substrate was ultrasonically cleaned with detergent, deionized water and isopropanol successively before use. A compact TiO2 layer about 90 nm was deposited on the FTO substrate by spin-coating 0.3 M 1-butanol solution of TDBA after UV-ozone treatment of the FTO substrate. After coating, the substrate was dried on a hot plate at 125 \\u00b0C for 5 min, and finally annealed at 500 \\u00b0C for 30 min. Equal molar FAI and PbI2 were mixed in DMF and stirred for 2 h to form a 1.0 M precursor solution. The perovskite FAPbI3 was deposited onto TiO2/FTO by spin-coating the precursor solution at 2500 rpm for 40 s before annealing on a hot plate at 150 \\u00b0C for 15 min. For the perovskite with SCN, an appropriate amount of NH4SCN was added into the FAPbI3 precursor solution and stirred for 2 h before use. The thickness of the perovskite without the additive and with 30 mol% NH4SCN is 400 nm and 480 nm, respectively. The spiro-OMeTAD hole transport layer solution was prepared by dissolving 72.5 mg spiro-OMeTAD, 28.8 \\u03bcL tBP and 17.5 \\u03bcL Li\\u2013TFSI solution (520 mg Li-TFSI in 1 mL acetonitrile) in 1 mL chlorobenzene. The prepared spiro-OMeTAD solution was spin-coated at 2500 rpm for 40 s and the thickness is 180 nm. Finally, a 10 nm MoO3 layer and 100 nm silver layer were deposited via thermal evaporation. TiO2 was prepared under ambient conditions and other device fabrication steps were carried out in a N2-purged glovebox.\\n\\nX-ray diffraction. Crystallographic properties of the perovskite films on TiO2/FTO substrates were investigated on a Rigaku UltimaIV X-ray diffractometer at room temperature using graphite monochromatic Cu K\\u03b1 radiation (1.5406 nm) with a scanning rate of 5 deg per min over the Bragg angle range of 10.0\\u201350.0\\u00b0.\\nUV-vis spectra. The UV-visible absorption spectra of the perovskite deposited on TiO2/FTO substrates were recorded on a UV-2450 UV-vis Shimadzu Spectrophotometer with the signal of the TiO2/FTO substrate as calibration background.\\nScanning electron microscope. Morphologies of the perovskite films on TiO2/FTO substrates were studied through SEM images obtained on an S-4800 (Hitachi) field-emission scanning electron microscope (FESEM) with a high tension of 3.0 kV and magnification of 3.0k.\\nMoisture stability test. FAPbI3 and 3S-FAPbI3 films were stored in a constant humidity and temperature chamber under dark conditions for 2 h, in which humidity and temperature were controlled to be RH 85% and 20 \\u00b0C, respectively.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 20.0; 20.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1,\\n Stability_PCE_initial_value: 5.94,\\n Stability_PCE_end_of_experiment: 9,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"TRUX-E-T. A solution of the compound 2,7,12-tribromo-5,5,10,10,15,15-hexahexyl-10,15-dihydro-5H-diindeno[1,2-a:1\\u2032,2\\u2032-c]fluorene (450.0 mg, 0.42 mmol) and 4-methoxy-N-(4-methoxyphenyl)-N-(4-(7-(tributylstannyl)-2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)phenyl)aniline (1.1 g, 1.49 mmol) in dry toluene (40 mL) was degassed twice with N2, and then Pd(PPh3)4 (71.9 mg, 0.062 mmol) was added. After stirring at 110 \\u00b0C for 48 h under N2, the mixture was cooled to room temperature. After the removal of toluene, the crude product was purified by column chromatography on silica gel (petroleum ether/ethyl acetate, 7:1, v/v) and recrystallized from methanol to afford TRUX-E-T (610.0 mg, 67.5%) as a light-yellow solid. 1H NMR (500 MHz, CDCl3, \\u03b4): 8.34 (d, J = 8.5 Hz, 3H), 7.85 (d, J = 8.1 Hz, 3H), 7.76 (s, 3H), 7.66\\u20137.58 (m, 6H), 7.09 (d, J = 8.4 Hz, 12H), 6.96 (d, J = 8.0 Hz, 6H), 6.89\\u20136.79 (m, 12H), 4.50\\u20134.34 (m, 12H), 3.81 (s, 18H), 2.93 (m, 6H), 2.18\\u20132.06 (m, 6H), 1.03\\u20130.78 (m, 36H), 0.68\\u20130.50 (m, 30H).13C NMR (125 MHz, CDCl3, \\u03b4): 156.25, 154.56, 147.68, 141.25, 139.16, 139.06, 138.12, 127.21, 126.88, 125.11, 124.26, 121.18, 119.65, 115.09, 65.14, 65.00, 56.10, 55.90, 37.52, 31.95, 29.98, 24.43, 22.73, 22.67, 14.42, 14.32. MALDI-TOF MS: m/z = 2177.0612 [M + H]+, calcd for C141H153N3O12S3: 2176.0616.\\n\\nPerovskite precursor. The MA0.7FA0.3PbI3 perovskite precursor was prepared using a mixture of methylammonium iodide (MAI, Dyesol), formamidinium iodide (FAI, Dyesol), lead iodide (PbI2, Alfa Aesar, 99.9985%) and lead thiocyanate (Pb(SCN)2, Sigma-Aldrich, 99.5%) in dimethyl sulfoxide (DMSO, Sigma-Aldrich) and N,N-dimethylformamide (DMF, Sigma-Aldrich). The details about the precursor preparation can be found in our previous papers. The precursor solution was stirred on a hotplate at 60 \\u00b0C for several hours. The resulting precursor was purified using a 0.45 \\u03bcm filter before spin-coating.\\nC60-SAM. The C60-self-assembly (SAM) (1-Materials) was used as purchased. C60-SAM has a concentration of 4 mg mL\\u22121 in chlorobenzene (Sigma-Aldrich, 99.8%).\\nSpiro-OMeTAD. 2,2\\u2032,7,7\\u2032-Tetrakis(N,N\\u2032-di-p-methoxyphenylamino)-9,9\\u2032-spirobifluorene (spiro-OMeTAD) was used to fabricate the reference HSLs and deposited on the perovskite film at 2000 rpm for 60 s. The spiro-OMeTAD was co-doped using Co(II)-bis-(trifluoromethanesulfonyl)imide (TFSI) and Li-TFSI. The spiro-OMeTAD solution was prepared by dissolving 72.3 mg spiro-OMeTAD (Shenzhen Feiming Science and Technology Co., Ltd.) in 1 mL chlorobenzene (CB) with 28 \\u03bcL 4-tert-butylpyridine (tBP) (Sigma-Aldrich), 18 \\u03bcL Li-TFSI (Sigma-Aldrich) (520 mg mL\\u22121 in acetonitrile) and 18 \\u03bcL Co(II)-TFSI salt (FK102, Dyesol) (300 mg mL\\u22121 in acetonitrile).\\nTRUX-E-T. A solution of TRUX-E-T/chlorobenzene (20 mg mL\\u22121) with an additive of 15 \\u03bcL Li-TFSI (170 mg mL\\u22121 in acetonitrile) and 8 \\u03bcL tBP.\\n\\nThe Fluorine-doped Tin Oxide (FTO) glass substrates were cleaned by ultra-sonication in diluted Micro-90 detergent, deionized water, acetone, and 2-propanol for 15 min, respectively. SnO2 ETLs were deposited on FTO using a plasma-enhanced atomic layer deposition (PEALD) method and then annealed on a hotplate at 100 \\u00b0C for 1 hour in ambient air (approximately 25 \\u00b0C and 55% relative humidity). The substrates were then transferred into a nitrogen filled glovebox. The C60-SAM solution was spin-coated onto the SnO2 layer at 3000 rpm for 1 min. The perovskite layer was deposited by dripping diethyl ether via an anti-solvent technique. The perovskite film was annealed at 100 \\u00b0C for 5 min. Spiro-OMeTAD was deposited on the perovskite film at 2000 rpm for 60 s. The TRUX-E-T was spin-coated on the perovskite film at 3500 rpm for 45 s, leading to an approximately 50 nm-thick layer. A layer of 50 nm gold was finally deposited on the top of the HSLs using thermal evaporation. The active area of the device was 0.08 cm2 as defined by a shadow mask during the Au evaporation. For hole-only devices, a 30 nm PEDOT:PSS layer was coated on an ITO substrate, followed by the deposition of a TRUX-E-T or a spiro-OMeTAD layer and then 8 nm MoO3, and 75 nm Ag layers. MoO3 and Ag were thermally evaporated to complete the device fabrication.\\n\\nCross-sectional scanning electron microscopy (SEM) image of the completed devices was taken with a Hitachi S-4800. Tapping-mode atomic force microscopy (AFM) images were taken with a Veeco Nanoscope V instrument. Layer thicknesses were determined using a Dektak surface profiler and cross-sectional SEM images. Samples were illuminated through the glass side for photoluminescence (PL) measurements. A 532 nm cw laser at 38 mW cm\\u22122 was used as a source of excitation for steady-state PL while a 532 nm pulsed laser (pulse width \\u223c5 ps) at \\u223c109 photons pulse\\u22121 cm\\u22122 was used as a source of excitation for TRPL measurement. PL decay curves were fitted by iterative re-convolution with the measured system response function. Mean photogenerated carrier lifetimes for the bi-exponential fit were calculated by the weighted average method.\\nJ\\u2013V curves were recorded in air under 100 mW cm\\u22122 AM1.5 G solar irradiation (PV Measurements Inc.) with a Keithley 2400 Source Meter. The light intensity for J\\u2013V measurements was calibrated by using a standard Si solar cell and our perovskite solar cells certified by Newport. External quantum efficiency (EQE) spectra were measured on a QE system (PV Measurements Inc., model IVQE8-C QE system without bias voltage) using 100 Hz chopped monochromatic light. The steady-state efficiencies were obtained by tracking the maximum output power point. The J\\u2013V curves for light intensity dependence were taken using neutral density filters between 1 and 100 mW cm\\u22122. The un-encapsulated cells for the stability test were stored in ambient air (45% humidity and room temperature). All characterizations and measurements were performed in ambient air.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c | C60-SAM,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: ALD | Spin-coating,\\n Perovskite_composition_long_form: FA0.3MA0.7PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: TRUX-E-T,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 25,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 480,\\n Stability_PCE_initial_value: 18.35,\\n Stability_PCE_end_of_experiment: 96.4,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Reagents and Materials: Tetrabutyl titanate, methylamine alcohol solution, N,N-dimethyl sulfoxide (DMSO), trimesic acid (TMA), lead iodide (PbI2, 99.9%), acetonitrile, N,N-dimethylformamide (DMF), methanol, isopropyl alcohol, n-butanol, ether, hydroiodic acid, 4-tert-butyl-pyridine, and lithium bis(trifluoromethylsulfonyl) imide (Li-TFSI) were obtained from Aldrich. The tetrabutyl titanate and acetylacetone were purchased from the Sinopharm Chemical Reagent Co. Ltd. Spiro-OMeTAD was gained from Xi'an Bolet Optoelectronics Technology Co., Ltd. The above agents were used for experiment directly. F-doped tin oxide (FTO) substrates were gained from NSG, Japan. CH3NH3I (MAI) and the TiO2 paste were prepared according to previous papers [,].\\nDevice fabrication: A TiO2 precursor solution was spin-coated on a cleaned FTO substrate at a spin rate of 500\\u202frpm for 9\\u202fs and 2500\\u202frpm for 30\\u202fs, and then annealed at 450\\u202f\\u00b0C for 30\\u202fmin to obtain the TiO2 compact layer. The TiO2 precursor solution was a mixed solution of 25\\u202fmL n-butanol, 5\\u202fmL tetrabutyl titanate, 5\\u202fmL isopropyl alcohol, 5\\u202fmL acetylacetone, and 0.6\\u202fmL emulsifier of Triton X-100. On the surface of compact TiO2, TiO2 paste was deposited (at 500\\u202frpm for 9\\u202fs and 2500\\u202frpm for 30\\u202fs) and followed by annealing at 450\\u202f\\u00b0C for 30\\u202fmin to obtain TiO2 electronic transport layer (ETL) []. 1.0\\u202fmol\\u202fL\\u22121 PbI2 precursor solution without or with a certain amount of TMA (mass ratio of TMA vs PbI2) in a mixed solvent (VDMF: VDMSO\\u202f=\\u202f7:3) was spin-coated on the TiO2 ETL at 500\\u202frpm for 9\\u202fs and 2500\\u202frpm for 30\\u202fs, then baked at 100\\u202f\\u00b0C for 10\\u202fmin to prepare the PbI2 films without or with TMA. After drying, MAI solution (100\\u202f\\u03bcL) was dropped on the PbI2 films, then the samples were allowed to rest for 1\\u202fmin and rinsed with isopropyl alcohol (500\\u202f\\u03bcL). Subsequently, the substrate was dried at 100\\u202f\\u00b0C to prepare the MAPbI3 films without or with TMA. The hole transfer layer (HTL) with a concentration of 65\\u202fmM Spiro-OMeTAD, 30\\u202fmM Li-TFSI and 200\\u202fmM 4-tert-butyl-pyridine was spin-coated on MAPbI3 film at 500\\u202frpm for 6\\u202fs and 2000\\u202frpm for 20\\u202fs. After 8\\u202fh in air under room temperature and 0.10% of humidity, the Ag electrode was deposited by thermal evaporation.\\nDevice characterization: The infrared spectrometric analyzer (BRUKER TENSOR 27) was used to record the fourier transform infrared (FTIR) spectra. The steady-state photoluminescence (PL) curves were performed using an Edinburgh Instruments FLS980. Field emission scanning electron microscope (FESEM) measurements were conducted using a JEOL-JSM-6701F operated at 10\\u202fkV. The powder X-ray diffraction (XRD) patterns were recorded using a BRUKER D8-ADVANCE. The ultraviolet to visible (UV\\u2013Vis) absorption spectra of films were measured using the Agilent 8453 UV\\u2013Vis diode array spectrophotometer. The photocurrent density-voltage (J-V) characteristic of the PSC was carried out using a computer-controlled CHI660D in ambient atmosphere. The incident light intensity was set under 100\\u202fmW\\u202fcm\\u22122 (AM 1.5\\u202fG). The active cell area was controlled to 0.09\\u202fcm2 by applying a black mask.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 100.0; 100.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 10,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 20,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"MAI and P3CT-N are synthesized in our lab according to previous report . PbI2, E2CA and PCBM are purchased from Alfa Aesar, Sigma-Aldrich and American Dye Source respectively. The solvent DMF and DMSO are obtained from Sigma-Aldrich and Alfa Aesar, respectively.\\n\\nThe ITO substrate (20\\u2009mm\\u2009*\\u200920\\u2009mm) is sequentially cleaned through ultrasonication in detergent, deionized water, acetone and isopropanol for 15\\u2009min respectively. The cleaned substrates are dried under N2 flow and then treated in O2 plasma for 2\\u2009min. The P3CT-N solution (1\\u2009mg/mL in methanol) is deposited on ITO substrate at 4000 r.p.m for 30\\u2009s, and then annealed at 100\\u2009\\u00b0C for 10\\u2009min. The perovskite precursor solution is prepared by mixing PbI2 (668.5\\u2009mg) and MAI (230.6\\u2009mg) in 1\\u2009mL DMF:DMSO (4:1\\u2009vol ratio). For solution containing E2CA, different amount E2CA is added into the clear solution of PbI2/MAI solution before fabrication. Perovskite layer is deposited using typical anti-solvent method in glovebox filled with N2. The perovskite precursor solution is spin-coated on ITO/P3CT-N at 4800 r.p.m. for 20\\u2009s. During spin-coating, 300\\u2009\\u03bcL chlorobenzene (Sigma-Aldrich) is dropped on the center of the substrate 12\\u2009s prior to the end of the program. The substrate is then annealed on hotplate at 80\\u2009\\u00b0C for 5\\u2009min to promote perovskite crystallization. For MAPbI3-E2CA, the perovskite films are further transferred to moisture air (relative humidity: 40\\u201360%) for 10\\u2009min to promote E2CA's polymerization. PCBM solution (10\\u2009mg/mL in chlorobenzene) is spin-coated on perovskite layer at 2000 r.p.m. for 45\\u2009s to form electron transporting layer. Finally, the substrate is transferred into vacuum chamber; 20\\u2009nm C60, 8\\u2009nm BCP and 100\\u2009nm Cu are thermally evaporated under high vacuum (1\\u2009*\\u200910\\u22124 Pa). The active area, as defined by the overlap of Cu and ITO, is 0.06 and 0.09\\u2009cm2.\\n\\nThe J-V curves are recorded using Keithley 2400 sourcemeter under the solar simulator (Newport Oriel Sol3A) with simulated AM 1.5\\u2009G illumination (100\\u2009mW\\u2009cm\\u22122). The light source is a 450\\u2009W xenon lamp calibrated by a standard Si reference solar cell (Newport, 91,150\\u2009V). Unless otherwise stated, The J-V curves are all measured in glovebox under forward scan from 1.2\\u2009V to \\u22120.2\\u2009V. The EQE measurement is conducted in air using Newport quantum efficiency measurement system (ORIEL IQE 200TM) combined with a lock-in amplifier and 150\\u2009W xenon lamp. The light intensity at each wavelength is calibrated by one standard Si/Ge solar cell.\\n\\nFTIR samples are prepared by scraping off perovskite layer from substrate and then mixed with pre-dried KBr powder. FTIR spectra are recorded in transmittance mode using IR spectrometer instrument (Thermo, Nicolet 6700).\\n\\nSEM images are recorded using field emission scanning electron microscope (Hitachi, S-4800) with an accelerating voltage of 8\\u2009kV. Cross-section SEM images are recorded with an accelerating voltage of 4\\u20138\\u2009kV according to the sample states.\\n\\nTEM images are recorded using JEOL2100, Japan. TEM samples are prepared by dropping perovskite solution (0.3\\u2009M) and then rapidly blowing dry on TEM grids. The samples are annealed at 100\\u2009\\u00b0C for 1\\u2009h and then collected in glass Petri dish to avoid the possible damage of grids.\\n\\nPL spectra are recorded with a Fluorolog-Horiba fluorometer with excitation wavelength at 450\\u2009nm. Time-resolved photoluminescence (TRPL) decays are conducted with excitation wavelength at 450\\u2009nm and emission wavelength at 770\\u2009nm.\\n\\nAir stability is recorded by storing the non-encapsulated devices in air with controlled humidity (40\\u201360%) at room temperature (~25\\u2009\\u00b0C). Before J-V measurement, the PSCs are put into a vacuum chamber for ~10\\u2009min to remove the moisture absorbed on surface.\\n\\nThermal stability is recorded by storing the non-encapsulated devices on a hotplate setting at 85\\u2009\\u00b0C in air (relative humidity: 40\\u201360%). The J-V curves are measured regularly by transferring PSCs into glovebox. Note that the PSCs are put into vacuum chamber for 5\\u201310\\u2009min and cooled to room temperature before measurement.\\n\\nLight stability is recorded by storing non-encapsulated devices under 1 sun illumination (white LED lamp) in air (relative humidity: 40\\u201360%). To calibrate the LED lamp illumination intensity, a perovskite solar cell is first measured under the solar simulator (Newport Oriel Sol3A) with simulated AM 1.5G illumination (450\\u2009W xenon lamp) to obtained a J sc. Then the perovskite solar cell is measured again under white LED lamp to reach the same J sc through regulate the intensity of LED lamp.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: E2CA,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: P3CT-N,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Cu,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 85.0; 85.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 200,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 68,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Indium tin oxide (ITO) with a sheet resistance of 7 \\u03a9 sq\\u22121 was purchased from CSG Holding Co., Ltd. DMF (N,N-dimethylformamide), DEACl (diethylammonium chloride) (99%) and MoS2 powder were bought from Sigma-Aldrich\\u00ae. PbI2 (99.999%), MAI (MA+ = CH3NH3+) (99.99%) and PCBM were bought from Xi'an Polymer Light Technology Corp. (PLT).\\n\\nGO used in this work was synthesized via a modified Hummers' method reported in our previous work. A total of 25 mL of concentrated sulfuric acid was instilled into a mixture of 1.0 g of graphite and 0.6 g of NaNO3 (sodium nitrate) at room temperature. Then, 3.7 g of KMnO4 (potassium permanganate) was added slowly to keep the reaction temperature below 5 \\u00b0C. Sulfuric acid was inserted into the graphite layers at this stage. The reaction temperature of the mixture was kept at 35 \\u00b0C with stirring for 2 h and then was increased to 60 \\u00b0C for heating for 6 h. Then, 45 mL of water was slowly poured into the solution under vigorous stirring, and a dark brown suspension was produced. The suspension was treated further by adding a mixture of aqueous hydrogen peroxide (3.5 mL, 34.5%) and water (22.5 mL) to convert the residual permanganate and manganese dioxide into soluble manganese sulfate. Graphene oxides were separated from the reaction mixture by ultrasonication. The graphene oxide powder was washed 3 times with diluted hydrochloric acid (1.0 mol L\\u22121, 25 mL). Ultrasonic treatment was carried out for 10 minutes before washing. The obtained product was dried for 24 h under vacuum and placed in a dryer with low humidity. The prepared GO was ground and dissolved in absolute ethyl alcohol with PEG. The concentrations of GO and PEG were 10 mg mL\\u22121 and 1 mg mL\\u22121, respectively. The fabricated solution was ultrasonically treated and stirred to be completely dissolved.\\n\\nPerovskite films deposited on different substrates such as PEDOT:PSS or its surface modified with GO:PEG were examined with field emission scanning electron microscopy (FESEM, HITACHI S-4700). The thicknesses of the films in perovskite solar cells used in this paper (shown in Fig. 1(b)) were measured with a step profiler (Dektak-150, Veeco) for PEDOT:PSS, perovskite, and PCBM and an atomic force microscope (AFM, Bruker icon) for GO:PEG (shown in Fig. S6\\u2020). The work-function of the film surfaces reported in this work was measured by ultraviolet photoemission spectroscopy (UPS) in ultra-high vacuum (UHV). UPS measurements were performed with an unfiltered He (21.22 eV) gas discharge lamp and a total instrumental energy resolution of 100 meV. The kinetic energy (EK) can be determined using the equation: where h\\u03bd is the energy of UV which is equal to 21.2 eV, EB is the binding energy in the original UPS spectrum. And the work function is the low energy cutoff of kinetic energy in the UPS spectrum.\\n\\nMAI, PbI2 and DEACl were dissolved in DMF with a molar ratio of 1:1:0.4. The concentration of MAI was 1 M (mol L\\u22121). The MAPbI3 solution was stirred on a hot plate at a temperature of 70 \\u00b0C for 12 hours. PEDOT:PSS (4083) was spin-coated on ITO, which was preheated on a hot plate at the temperature of 75 \\u00b0C for 5 min, at a speed of 3000 rpm for 30 seconds and annealed on a hot plate at 130 \\u00b0C for 15 minutes in a N2 glovebox. Some samples were treated with the prepared GO:PEG solution. The GO:PEG solution was spin-coated on the PEDOT:PSS film at a rate of 3000 rpm for 30 s and annealed on a hot plate at a temperature of 90 \\u00b0C for 30 min. The MAPbI3 and DEACl mixture solution was spin-coated on top of the substrates with the PEDOT:PSS or PEDOT:PSS/GO:PEG layer to produce a perovskite film with the rate of 4000 rpm for 30 seconds, and annealed on a hot plate at 90 \\u00b0C for 10 minutes. After the perovskite film was formed, an ETL (electron transfer material) (15 mg of PCBM was added into 1 mL of chlorobenzene) was spin-coated on top of the perovskite film at a rate of 1500 rpm for 30 seconds. Finally, different thicknesses of molybdenum disulfide (MoS2) and 140 nm of silver (Ag) were successively deposited on top of the PCBM layer via a thermal evaporation process in a vacuum chamber with a pressure of less than 10\\u22124 Pa. The typical active area of the devices was approximately 0.12 cm2, as determined using a shadow mask during the top electrode evaporation. The solar light source was simulated by AM 1.5 sunlight with the intensity of 100 mW cm\\u22122 provided by a solar simulator. The current density (J)\\u2013voltage (V) was recorded using a Keithley 2400 source meter unit. The external quantum efficiency (EQE) measurements were carried out with a quantum efficiency (QE)/IPCE measurement system (SR830, Stanford Research Systems). A standard Si photodiode calibrated from Hamamatsu was tested as a reference prior to each sample measurement. J\\u2013V measurements were carried out in a N2 glovebox, and EQE was measured in air under the conditions of the devices with encapsulation. Steady-state measurements of the solar cell devices were carried out with an electrochemical workstation (CS150H, Wuhan Corrtest Instruments Corp., Ltd.). In the stability tests, the device was tested under continuous illumination in a glovebox with no encapsulation. The steady-state power output of the perovskite solar cells was measured real-time under a constant voltage bias at the maximum power-point. Time-resolved transient photoluminescence (PL) spectra were obtained using a PL spectrometer, FLS 900, Edinburgh Instruments, excited with a picosecond pulsed diode laser (EPL-445) and measured at 405 nm after excitation. Electrochemical impedance spectra (EIS) measurements were done using a frequency response analyzer (PSM1735 NumetriQ) from 1 Hz to 106 Hz under dark conditions at a 1 V applied bias.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | MoS2,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: DEACl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS | Graphene oxide; PEG,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials: PEDOT:PSS (Baytron PVPAI 4083) used for comparison was supplied by Heraeus Holding GmbH .-phenyl-C61-butyric acidmethylester (PCBM) and bathocuproine (BCP) were bought from Nano-C. Methylammoniumiodide (MAI) was received from 1-Material. All other chemicals used in this work were analytical grade including lead(II) iodide (PbI2), lead(II) chloride (PbCl2), dimethyl sulfoxide (DMSO), \\u03b3-butyrolactone (GBL), ammonium persulphate (APS), acetone, formaldehyde (37\\u00a0wt%), and so on.\\nPreparation of SAF and PEDOT:SAF: SAF was synthesized by polymerization and sulfonation of formaldehyde, acetone and sodium sulphite (molar ratio 2:1:0.6) in alkaline condition. 8.2\\u00a0g of Na2SO3 solid was dissolved in 20\\u00a0mL of deionized water at 45\\u00a0\\u00b0C and adjusting its pH to 10 by NaOH (20%). Then, 16\\u00a0mL of formaldehyde (37%) and 8.0\\u00a0mL of acetone were added rapidly. The polymerization was stopped after 5\\u00a0h of reflux at 85\\u00a0\\u00b0C and the mixture became brownness. The residual reactants were removed by vacuum rotary evaporation, and its pH value was adjusted to 2\\u20133 by addition of HCl (20%). The solid content of the obtained raw product which will be directly used to prepare PEDOT:SAF is 14.5%. PEDOT:SAF aqueous dispersion was prepared using the unpurified SAF liquor as follows. 5.0\\u00a0g of SAF liquor and 1.0\\u00a0g of EDOT were added into 50\\u00a0mL deionized water (mass ratio of EDOT:SAF was 2:1). After stirring slowly for 10\\u00a0min, the pH of the solution was adjusted to 2 by HCl (20%). Then, 1.9\\u00a0g of APS used as oxidant was dissolved in water (5\\u00a0mL) and added in drops. The reaction was kept under high stirring speed (700 rps) and room temperature after the EDOT monomers being completely reacted (about 48\\u00a0h). For the following characterization, the products were purified by using a dialysis membrane (MWCO 1000\\u00a0Da) for 5\\u20137 days. The mass fraction of PEDOT:SAF was concentrated to more than 1.2\\u00a0wt% by rotary evaporation quantified by UV absorption at the wavelength of 800\\u00a0nm.\\nCharacterization of SAF and PEDOT:SAF: FTIR spectra were performed using the KBr pellets in the 4000-400\\u00a0cm\\u22121 region by Auto system XL/I-series/Spectrum 2000 spectrometry (Thermo Nicolet Co., Madison, WI, USA). Element contents of C, H and S were rationed by Vario EL cube (Elementar, Germany) with about 5.0\\u00a0mg packed in aluminized paper. UV\\u2013vis absorption and transmittance spectra were measured by Shimadzu UV-3600 spectrophotometer (Japan) and Shimadzu UV-2600 spectrophotometer (Japan), respectively. Photoluminescence (PL) spectra were detected on F-4500 fluorescence spectrometer (Hitachi, Japan) with photomultiplier tube voltage of 400\\u00a0V. Dynamic light scattering (DLS) experiments were performed on a Zeta PALS instrument (Brookhaver, America). Cyclic voltammetry (CV) test was conducted with a film on glassy carbon electrode against Ag/AgCl (3\\u00a0M KCl solution) reference electrode at scanning rate 100\\u00a0mV/s. The conductivity and sheet resistance of PEDOT:PSS and PEDOT:SAF films were measured with a KDY-1four point probes resistivity/resistance measurement system. The films were prepared by dropping the sample on glass and air drying at room temperature. The films thicknesses were tested by a step profiler (Dektak150, Veeco, USA). UPS and XPS measurements were conducted on a Thermo Scientific ESCALAB 250Xi with a He(\\u0399) UV source (21.22\\u00a0eV) in ultrahigh vacuum. For testing UPS and XPS, the samples were spin-coated onto ITO glass and kept in an oven at 110\\u00a0\\u00b0C for 15\\u00a0min before the measurement, and all of the experimental processes were conducted in ultrahigh vacuum environment. Atomic force microscopy (AFM) images (height and phase images) were observed by a Park XE-100 in tapping mode. Surface wettability was measured using a static contact angle instrument (Powereach JC2000 C1, Shanghai, China).\\nFabrication and Characterization of PSCs: The configurations of PSCs were ITO/HELs/CH3NH3PbI3-xClx/PC61BM/BCP/Ag. ITO-coated glass substrates were cleaned via a series of ultrasonication in detergent, acetone, DI water, isopropyl alcohol and followed by UV-ozone plasma treatment. PEDOT:SAF layer was spin-coated onto the pre-patterned ITO glass substrate and annealed using a hot plate at 140\\u00a0\\u00b0C for 15\\u00a0min to remove residual solvents. PEDOT:PSS (Baytron PVPAI 4083) based device was also fabricated as comparison with the same method. The substrates with PEDOT:SAF or PEDOT:PSS were then transferred into a glove box filled with highly pure N2. Then MAPbI3-xClx precursor solution (1.26\\u00a0M PbI2, 0.14\\u00a0M PbCl2 and 1.35\\u00a0M MAI in cosolvent of DMSO:GBL at vol ratio of 3:7) was spin-coated to form a perovskite layer of about 280\\u00a0nm on the modified ITO substrate. After annealing at 100\\u00a0\\u00b0C for 20\\u00a0min, the PCBM layer (\\u223c55\\u00a0nm) was deposited by spin coating onto the surface of perovskite layer. Then, 0.5\\u00a0mg/mL BCP solution was spin coated onto PCBM layer. The devices were completed by thermal deposition a layer of 100\\u00a0nm Ag as cathode in a vacuum of <1\\u00a0\\u00d7\\u00a010\\u22126\\u00a0Torr. The devices area was 0.07\\u00a0cm2 defined by shadow mask. The photovoltaic performance of the PSCs was tested in air with a computer-programmed Keithley 2400 source/meter and a Newport's Oriel class solar simulator, which simulated the AM1.5 sunlight with energy density of 100 mW/cm2 and was certified to the JIS C 8912 standard. IPCEs of PSCs were measured with a 300\\u00a0W Xenon Lamp (Oriel 6258) and a Cornerstone 260 Oriel 74125 monochromator. The photovoltaic stability of PSCs was investigated by storing the unencapsulated devices in glovebox with humidity below 0.1 ppm and normal room light for 28 days. For the perovskite layer, UV\\u2013visible absorption spectra of were measured on a Perkin-Elmer Lambda 950 spectrophotometer. Photoluminescence spectra were collected on an Edinburgh Instruments FLS920 spectrofluorometer, the excitation wavelength was 630\\u00a0nm. Scanning electron microscopy (SEM) images were obtained on a JSM-7800F SEM. Thin film X-ray diffraction (XRD) measurements were conducted on a Bruker D8 Advance XRD instrument.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Compared with the isotropic metallic NPs (i.e., spheres), anisotropic metallic NPs with the shape of prism are utilized as the interfacial layer because they can excite SPP resonances over a wider wavelength range and exhibit a larger extinction ratio due to the stronger surface charge polarizability induced by large shape asperities []. In particular, AuAg-alloyed nanoprisms (AuAg-NPrisms in short) are utilized due to their higher stability than the pure Ag nanoprisms (Ag-NPrisms) [], and improved performances have already been demonstrated in organic solar cells with AuAg-NPrisms [,]. Here, the AuAg-NPrisms were prepared using a two-step synthesis method []. First, Ag-NPrisms were synthesized by the seed-mediated approach. Then, the galvanic replacement approach is adopted to turn Ag-NPrisms into AuAg-NPrisms. At last, the AuAg-NPrisms were coated with a thin SiO2 shell (represented by AuAg-NPrisms@SiO2) to prevent exciton quenching using the method of hydrolysis of tetraethyl orthosilicate (TEOS). This product was used as the interfacial layer for making highly crystalline quasi-2D PEA based perovskite film. In the solar cell device, the poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS) layer is pre-coated ahead the perovskite film. In order to spin-coat the AuAg-NPrisms@SiO2 on top of the PEDOT:PSS layer without dissolving the underlying PEDOT:PSS layer, it is necessary to change the solution to ethanol by twice centrifugation (7000\\u202frpm, 20\\u202fmin).\\nThe proposed PSCs with an metallic interfacial layer has an architecture of ITO/PEDOT:PSS/AuAg-NPrism@SiO2/(PEA)2(MA)2Pb3I10/PC61BM/PFN/Ag as shown in Fig. 1 (a). Here, PEA based perovskite crystals with a chemical formula of (PEA)2(MA)2Pb3I10 (here, n\\u202f=\\u202f3) is applied as the active layer for absorbing light and generating excitons. The exciton dissociation takes place in the bulk perovskite layer and at the PEDOT:PSS/perovskite and perovskite/PC61BM interfaces as well. For the cathode buffer layer, besides of PC61BM, an additional poly[(9,9-bis (3\\u2019-(N, N-dimenthylamino)propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctyfluorene)] (PFN) layer is introduced to further reduce the dark current. The thicknesses of PEDOT:PSS, (PEA)2(MA)2Pb3I10, PC61BM and PFN layers are measured to be 30\\u202fnm, 60\\u202fnm, 25\\u202fnm and 15\\u202fnm, respectively. The corresponding energy band diagram of the control PSCs is given in Fig. 1(b). On the basis of the control PSCs, the proposed metallic NP modified PSCs are realized via spin-coating the synthesized AuAg-NPrisms@SiO2 solution on the top of the PEDOT:PSS layer.\\nThe details of the fabrication of the proposed PSCs are as follows. The ITO glass substrate is cleaned sequentially in detergent, deionized water, isopropanol, and acetone. Then the PEDOT:PSS layer is spin-coated onto the ITO glass substrates at 7000\\u202frpm for 30\\u202fs in air and the sample is annealed on a hot plate at 125\\u202f\\u00b0C for 15\\u202fmin. Subsequently, the synthesized AuAg-NPrisms@SiO2 solution at different concentrations is span coated on the top of the PEDOT:PSS layer at 2000\\u202frpm/min for 30\\u202fs and then the sample was annealed at 120\\u202f\\u00b0C for 10\\u202fmin. Next, the quasi-2D perovskite (PEA)2(MA)2Pb3I10 (PEA = C6H5(CH2)2NH3 +) solution is spin-coated at 2000\\u202frpm for 45\\u202fs and annealed on a hot plate at 70\\u202f\\u00b0C for 10\\u202fmin in a nitrogen glovebox. Here, the (PEA)2(MA)2Pb3I10 solution is prepared by mixing No. 1 solution with No. 2 solution by a volume ratio of 2:1, where No. 1 solution was prepared by dissolving 159\\u202fmg MAI and 461\\u202fmg PbI2 in a 2\\u202fmL anhydrous dimethylformamide (DMF) solvent and No. 2 solution was prepared by dissolving 498\\u202fmg PEAI and 461\\u202fmg PbI2 in a 2\\u202fmL DMF solvent. In the following, the PCBM solution is spin-coated at 2700\\u202frpm for 30\\u202fs and then PFN is spin-coated at 7000\\u202frpm for 30\\u202fs. Finally, a 100\\u202fnm Ag electrode is deposited by thermal evaporation. The active area of each fabricated quasi-2D PSC device was about 0.04\\u202fcm2, determined by the overlap of the ITO anode and Ag cathode.\\nMorphologies of AuAg-NPrism@SiO2 are examined by the transmission electron microscopy (TEM JEM 2010) and the absorption spectra of AuAg-NPrism@SiO2 are measured by a UV\\u2013visible spectrophotometer (Shimadzu 2600). The electrical performances of the solar cells are measured with a source meter (Keithley 2400) when the samples are under AM 1.5G solar spectrum illumination at 100\\u202fmW/cm2 (ABET Technologies, Sun 3000). The external quantum efficiencies (EQE) of PSCs are characterized by ZOLIX CSC1011. Surface morphologies of the (PEA)2(MA)2Pb3I10 films are examined by atomic force microscopy (AFM, SPA-3000HV). Absorption spectra of multiplayer films are characterized by the UV\\u2013visible spectrophotometer (Shimadzu 2600). Edinburgh Instruments FLS980 is used to characterize the steady-state photoluminescence (PL) spectra of multilayer films.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PFN,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: (PEA)2MA2Pb3I10,\\n Perovskite_composition_short_form: (PEA)MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fig. 1a, S1 and S2\\u2020 illustrate the synthetic routes of TDT-OMeTPA and TTPA-OMeTPA. Compound 3 was synthesized by reported procedures. The first three steps of the synthesis of TDT-OMeTAD are described in the ESI\\u2020 and compounds 3 and 4 are characterized by 1H NMR in Fig. S13 and S14 (ESI\\u2020).\\nSynthesis of TDT-OMeTPA. In a 50 mL two-necked flask, N,N\\u2032-dimethoxydiphenylamine (0.76 g, 3.31 mmol), compound 4 (1.0 g, 0.95 mmol), sodium tert-butoxide (0.36 g, 3.8 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.026 g, 0.028 mmol) and tri-tert-butylphosphine (0.017 g, 0.08 mmol) were mixed. Next, 15 mL of anhydrous toluene was added into the flask under a nitrogen atmosphere. The reaction mixture was heated to reflux at 125 \\u00b0C for 36 h under a nitrogen atmosphere. After cooling to room temperature, the reaction mixture was extracted with ethyl acetate and brine water, followed by drying with anhydrous MgSO4. After the solvent had evaporated the residue was purified by column chromatography (ethyl acetate/ether = 1/5) to afford a beige solid in 74% yield (0.99 g). 1H NMR (CDCl3, 400 Hz, Fig. S15, ESI\\u2020): \\u03b4, [ppm]: 2.184 (s, 24H), 3.682 (s, 24H), 6.222 (s, 6H), 6.445 (d, 12H, J = 8.4 Hz), 6.701 (s, 12H), 6.806 (s, 12H, J = 8.4 Hz). Anal. calcd for C105H90N4O6: C, 83.86%; H, 6.03%; N, 3.73%. Found: C, 83.80%; H, 6.06%; N, 3.70%. MS (MALDI-TOF): calcd for C105H90N4O6, 1503.86; found, 1503.817. The FT-IR spectrum of TDT-OMeTPA is shown in Fig. S16 (ESI\\u2020).\\nSynthesis of TTPA-OMeTPA. In a 50 mL two-necked flask, tri(4-bromophenyl)amine (1.5 g, 3.11 mmol), N,N\\u2032-dimethoxydiphenylamine (5 g, 21.8 mmol), sodium tert-butoxide (2.39 g, 24.9 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.171 g, 0.18 mmol) and tri-tert-butylphosphine (0.113 g, 0.54 mmol) were mixed. Next, 15 mL of anhydrous toluene was added into the flask under a nitrogen atmosphere. The reaction mixture was heated to reflux at 125 \\u00b0C for 24 h under a nitrogen atmosphere. After cooling to room temperature, the reaction mixture was extracted with ethyl acetate and brine water, followed by drying with anhydrous MgSO4. After the solvent had evaporated the residue was purified by column chromatography (ethyl acetate/ether = 1/5) to afford a beige solid in 89% yield (1.93 g). 1H NMR (CDCl3, 400 Hz, Fig. S17, ESI\\u2020): \\u03b4, [ppm]: 3.81 (s, 18H), 6.88 (m, 24H), 7.06 (m, 12H). Anal. calcd for C60H54N4O6: C, 77.73%; H, 5.87%; N, 6.04%. Found: C, 77.80%; H, 5.83%; N, 6.02%. MS (MALDI-TOF): calcd for C60H54N4O6, 927.09; found, 927.098. The FT-IR spectrum of TTPA-OMeTPA is shown in Fig. S16 (ESI\\u2020).\\n\\nThe FTO (F-doped SnO2, Pilkington, TEC8) glasses were cleaned in an ultrasonic bath with detergents, acetone, and deionized water respectively for 30 min, and then a blocking layer of TiO2 (60 nm, bl-TiO2) was deposited onto the FTO glass by spray pyrolysis using a 20 mM titanium diisopropoxide bis(acetylacetonate) solution (Aldrich) at 450 \\u00b0C. A mesoporous TiO2 layer was spin-coated on the top of the bl-TiO2/FTO substrate at 1000 rpm for 60 s using a TiO2 (\\u223c50 nm particle size) paste. The pristine TiO2 paste was diluted in 2-methoxyethanol (1 g/5 mL). The mesoporous TiO2 layer was annealed at 550 \\u00b0C for 30 min in air, which led to a thickness of about 100 nm. These substrates were further treated with 40 mM TiCl4 aqueous solution for 30 min at 70 \\u00b0C, followed by rinsing with deionized water and ethanol and vacuum drying (overnight). The (FAPbI3)0.92(MAPbBr3)0.08 perovskite solution (with a small excess of PbI2) was coated onto the mp-TiO2/bl-TiO2/FTO substrate (70 \\u00b0C) by two consecutive spin-coating steps at 1000 and 4000 rpm for 5 s and 10 s, respectively. During the second spin-coating step, 0.5 mL ethyl ether was poured onto the substrate. The 1.05 M solution for the (FAPbI3)0.92(MAPbBr3)0.08 perovskite was prepared by dissolving FAI (NH2CHNH2I) and MABr (CH3NH3Br) with PbI2 and PbBr2 in DMF (N,N-dimethylformamide) and DMSO (dimethylsulfoxide) (6:1 v/v). The perovskite-deposited substrate was then dried on a hot plate at 100 \\u00b0C for 10 min. TTPA-OMeTPA, TDT-OMeTAD and Spiro-OMeTAD were spin-coated at 4000 rpm for 60 s from a chlorobenzene solution (68 mmol L\\u22121) containing Li-TFSI (Li-bis(trifluoromethanesulfonyl) imide, 9 mmol L\\u22121) and TBP (tert-butylpyridine, 55 mmol L\\u22121) as dopants. Finally, a 120 nm Ag electrode was deposited by thermal evaporation under a high vacuum.\\nA Keithley 2400 source meter and a Newport 3A monochromator were used for the J\\u2013V characterization of the PSCs. The J\\u2013V curves of all the devices were measured by masking the active area with a metal mask with an area of 0.085 cm2. The photocurrent action spectra (IPCE vs. wavelength) were measured with an incident photon\\u2013current conversion efficiency (IPCE) test system. The modulation frequency was about 2 Hz and the light source from a 300 W xenon lamp (Oriel 6258) was focused on a computer-controlled monochromator (Cornerstone 260 Oriel 74125) to select a single wavelength with a resolution of 10 nm. An NREL traceable Si detector (Oriel 71030NS) was applied to measure the light intensities and an optical power meter (Oriel 70310) was employed to measure the short circuit currents of the PSC devices.\\n\\nA device configuration of glass/perovskite/HTM was used in the measurement of photoluminescence (PL) and time-resolved photoluminescence (TR-PL) using a Fluo Time 300. An excitation wavelength of 600 nm was employed during PL measurement. The light was induced at the side of the glass.\\n\\nAll calculations were performed using the Gaussian09 program package. Density functional theory (DFT) calculations were utilized to optimize the ground-state geometry of NUIST1 with the Lee\\u2013Yang\\u2013Parr function (B3LYP), and the 6-31G basis set was used for all atoms. The time-dependent density functional theory (TD-DFT) calculation was used in calculating the electronic transitions based on the optimized ground-state structure.\\n\\nThe hole-only devices of TDT-OMeTPA, TTPA-OMeTPA and Spiro-OMeTAD with the structure ITO/PEDOT:PSS/HTM/Ag (ITO = indium tin oxide, PEDOT:PSS = poly(3,4-ethylenedioxythiophene):polystyrene sulfonate) were fabricated to test the hole mobility values of the HTMs. The current density\\u2013voltage curves were recorded with a Keithley 2400 source. The thicknesses of the HTM layers are around 100\\u2013200 nm and the hole mobility values were calculated using the Mott\\u2013Gurney law.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: TDT-OMeTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Ambient,\\n Stability_time_total_exposure: 500,\\n Stability_PCE_initial_value: 16.4,\\n Stability_PCE_end_of_experiment: 95,\\n Cell_area_measured: 0.085,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless stated otherwise, all of chemicals and solvents were purchased from Sigma-Aldrich and TCI, Ltd, and used without further purification. The p-DTS(FBTTh2)2 and PCDTBT were purchased from Nano clean tech.\\n\\nThe UV-vis absorption spectra of the hole transporting materials were obtained using a PerkinElmer Lambda 35 UV-vis spectrometer. Cyclic voltammetry (CV) was measured as thin films in acetonitrile solution containing 0.1\\u202fM of tetrabutylammoniumhexafluorophosphate (Bu4NPF6) as supporting electrolyte using CH instruments electrochemical analyzer. Indium tin oxide (ITO) as the working electrode, a Pt wire as the counter electrode, and an Ag/AgCl electrode as the reference electrode were used as a three-electrode system at a scan rate of 50\\u202fmV\\u202fs\\u22121. Grazing incidence X-ray diffraction (GIXD) were measured using the synchrotron radiation source 9A beamline at the Pohang Accelerator Laboratory. Atomic force microscopy (AFM) images were obtained by using an XE-100 (Park system) in a noncontact mode. Water contact angle on HTM films were measured using an automatic microscopic contact angle meter (PCA-1, Kyowa Interface Science). Cross-sectional scanning electron microscope (SEM) S-3 images were obtained using FEI Inspect F50.\\n\\nTo prepare the perovskite solar cell, we firstly etched the some parts of F-doped SnO2 (FTO, Pilkington, TEC 8) glass substrates (FTO glass size\\u202f=\\u202f2.5\\u202fcm\\u202f\\u00d7\\u202f2.5\\u202fcm: etched area\\u202f=\\u202f1\\u202fcm\\u202f\\u00d7\\u202f2.5\\u202fcm, unetched area\\u202f=\\u202f1.5\\u202fcm\\u202f\\u00d7\\u202f2.5\\u202fcm). After the FTO etching process, we sequentially washed the etched FTO glass substrates using ultrasonicator with 5% Hellmanex soap, ethanol, acetone, and then treated the FTO glass substrates by Ar plasma to remove the organic residues. A dense TiO2 electron conducting layer with a \\u223c50\\u202fnm-thickness was deposited on the partially etched the FTO glass substrate by a spray pyrolysis deposition method with a 20\\u202fmM of titanium diisopropoxide bis(acetylacetonate)/ethanol (Aldrich) solution at 450\\u202f\\u00b0C. A 40\\u202fwt% MAPbI3 perovskite solution was prepared as follows: 1:1\\u202fmol ratio of methyl ammonium iodide (MAI, DS LOGICS CO, LTD.) and lead (II) iodide (PbI2, Aldrich) were reacted in 1\\u202fmL\\u202fN,N-dimethyl formamide (DMF, Aldrich) at 60\\u202f\\u00b0C for 30\\u202fmin and then, 100\\u202f\\u03bcL hydriodic acid (HI, Aldrich) was added into the solution. The 40\\u202fwt% MAPbI3 perovskite solution was spin-coated on the TiO2/FTO substrate at 3000\\u202frpm for 200\\u202fs and then dried on the hot plate at 100\\u202f\\u00b0C for 2\\u202fmin. For hole transporting layers, we prepared three different composition of hole transporting material solution such as p-DTS(FBTTh2)2/chlorobenzene (10\\u202fmg\\u202fmL\\u22121), p-DTS(FBTTh2)2/chlorobenzene (10\\u202fmg\\u202fmL\\u22121) with 1 v/v% DIO, and p-DTS(FBTTh2)2/chlorobenzene\\u00a0+\\u00a06\\u00a0wt% PCDTBT (10\\u00a0mg\\u00a0mL\\u22121) with 1 v/v% DIO and then coated on the MAPbI3/bl-TiO2/FTO substrates by spin coating at 3000\\u202frpm 60\\u202fs. Finally, an Au layer was deposited with a 60\\u202fnm thickness by thermal evaporation. Whole experiments were performed in an ambient atmosphere under controlled relative humidity below 30%. The active area of each solar cell is 0.16\\u202fcm2.\\n\\nThe current density versus voltage (J-V) characteristics of perovskite solar cell devices were recorded on a potentiostat (IVIUM, IviumStat). A class-A solar simulator with a 1000\\u202fW Xenon lamp (Peccell, PEC-L01) was employed as a light source. Its light intensity was adjusted to AM 1.5G 1 sun light intensity (100\\u202fmW\\u202fcm\\u22122) using a calibrated Si-reference cell certificated by JIS. The external quantum efficiency (EQE) was measured as a function of wavelength from 300 to 900\\u202fnm on an incident photon-to-current conversion equipment (HS technologies). The EQE measurement system consisted of a power source (ABET, 150\\u202fW Xenon lamp, 13014), a monochromator (DONGWOO OPTRON Co, Ltd, MonoRa-500i), and potentiostat (IVIUM, IviumStat). Calibration was performed using a silicon photodiode G425, which is National Institute of Standard and Technology (NIST) calibrated as a standard. For hole mobility measurements, hole only devices with ITO/PEDOT:PSS/HTMs/Au structure were fabricated. Mobilities of HTMs were calculated from the J-V curves measured in dark by space charge limited current (SCLC) method, based on the following equation: J=98\\u03b50\\u03b5r\\u03bchV2L3 where \\u03b5 o is the permittivity of free space, \\u03b5 r is the dielectric constant of HTMs, \\u03bc h is the hole mobility, V\\u202f=\\u202fV appl \\u2013V bi \\u2013V a (where V appl is the applied bias, V bi is the built-in potential due to the difference in electrical contact work function, and V a is the voltage drop due to contact resistance and series resistance across the electrodes), and L is the thickness of the HTMs layer. The current density versus voltage characteristics were also recorded on a Keithley model 2400 source measuring unit. The perovskite solar cell devices based on HTMs were fabricated by same procedures in the previous report [].\\n\\nTime-resolved photoluminescence (TRPL) measurement was performed using an inverted-type scanning confocal microscope (MicroTime-200, Picoquant, Germany) with a 60\\u202f\\u00d7\\u202f(air) objective. A single-mode pulsed diode laser (470\\u202fnm with a \\u223c30 ps pulse width and a \\u223c0.1\\u202f\\u03bcW average power) was used as an excitation source. A dichroic mirror (490 DCXR, AHF), a long-pass filter (HQ500lp, AHF), a 75\\u202f\\u03bcm pinhole, a 700\\u202fnm long-pass filter, and a single photon avalanche diode (PDM series, MPD) were used to collect emissions from the samples. Exponential fittings for the obtained fluorescence decays were performed using the Symphotime-64 software by an exponential decay model; (t)=\\u2211Aie\\u2212t/\\u03c4i, where I(t) is the time-dependent PL intensity, A is the amplitude, and \\u03c4 is the PL lifetime.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: HI,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: p-DTS(FBTTh2)2,\\n HTL_additives_compounds: DIO,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 85.0; 85.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 2,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped tin oxide (FTO) glass (Nippon Electric Glass, 15\\u00a0\\u03a9 sq\\u22121) was partially etched to control the conductive area by Zinc powder and hydrochloric acid (35\\u00a0wt%). The FTO substrates were cleaned by sonication in diluted Decon-90 detergent (5\\u00a0wt% in H2O), deionised water, acetone and isopropanol in sequence. The cleaned substrates were dried with a N2 flow and treated by UV-Ozone for 20\\u00a0min to enhance surface wettability. 0.15\\u00a0M titanium diisopropoxide bis(acetylacetonate) (75\\u00a0wt% in isopropanol, Sigma-Aldrich) was dissolved in anhydrous 1-butanol with 5\\u00a0wt% acetylacetone and dripped onto the FTO substrates followed by spin-coating at 2000\\u00a0rpm for 20\\u00a0s to obtain a compact TiO2 (c-TiO2) layer. The film was dried at 125\\u00a0\\u00b0C for 5\\u00a0min and annealed at 500\\u00a0\\u00b0C in air for 1\\u00a0h. A TiO2 nano particle paste (30-NRD, Greatcell Solar) was diluted to a dispersion (0.1\\u00a0g\\u00a0ml\\u22121)\\u00a0by absolute ethanol and spin-coated onto the c-TiO2 film at 2000\\u00a0rpm for 20\\u00a0s as a mesoporous TiO2 (m-TiO2) layer. The m-TiO2 film was again sintered at 500\\u00a0\\u00b0C in air for 1\\u00a0h.\\nThe fabrication of perovskite films was operated in a N2-filled glove box. Cs0.05MA0.16FA0.79PbI2.5Br0.5 precursor was prepared by dissolving 1.1\\u00a0M PbI2 (99.9%, Youxuan Tech, China), 0.2\\u00a0M PbBr2 (99.999%, Sigma-Aldrich), 1\\u00a0M FAI (Greatcell Solar) and 0.2\\u00a0M MABr (Greatcell Solar) in a mixed DMSO/DMF (v:v\\u00a0=\\u00a01:4) solvent. 1.5\\u00a0M CsI was dissolved in DMSO and then added into the perovskite solution for the desired molar ratio of 5%. 72.3\\u00a0mg Spiro-MeOTAD (2, 2\\u2032, 7, 7\\u2032-Tetrakis- (N, N-di-4-methoxyphenylamino)-9, 9\\u2032-spirobifluorene, Borun New material, China), 29\\u00a0\\u03bcl 4-tert-butylpyridine (98%, Sigma-Aldrich) and 35\\u00a0\\u03bcl Li-TFSI (bis(trifluoromethane)sulfonimide lithium, Sigma-Aldrich)/Co(III)-TFSI (FK 209, Greatcell Solar) mixed solution (260\\u00a0mg Li-TFSI and 71.5\\u00a0mg Co(III)-TFSI in 1\\u00a0ml acetonitrile) were dissolved in 1\\u00a0ml chlorobenzene for the preparation of the hole transporting layer (HTL).\\nThe deposition of perovskite layer onto the m-TiO2 layer employed a two-step program with a spin-coating process at 2000\\u00a0rpm for 10\\u00a0s first (acceleration of 200\\u00a0rpm\\u00a0s\\u22121) followed by a second procedure at 6000\\u00a0rpm for 20\\u00a0s (acceleration of 2000\\u00a0rpm\\u00a0s\\u22121). 0.15\\u00a0ml chlorobenzene as an antisolvent was dripped onto the films at the 25th s before the program ended. The perovskite layer was then annealed at 100\\u00a0\\u00b0C for 45\\u00a0min. After cooling down to room temperature, the HTL was prepared by spin-coating the Spiro-MeOTAD solution onto the perovskite film at 4000\\u00a0rpm for 30\\u00a0s. The samples were then stored in a black box with dry air (relative humidity <20%) overnight for oxidization of the HTL. Finally, a gold layer with the thickness of 100\\u00a0nm was deposited as the back electrode using an e-beam evaporation system at 10\\u22126\\u00a0Torr pressure.\\n\\n20\\u00a0\\u03bcl ethylenediamine (EDA), diethylenetriamine (DETA) and triethylenetetramine (TETA) were dripped on the bottom of glass petri dishes followed by shakes for 10\\u00a0s to obtain a uniform spread. The complete devices were covered by the overturned glass petri dishes at room temperature in a glove box. Since the boiling points of the three solvents are relatively high (116\\u00a0\\u00b0C, 204\\u00a0\\u00b0C and 278\\u00a0\\u00b0C), the PSCs were gradually treated by the ligand vapours. To investigate the optimum condition for device performance, the duration of the treatment was scheduled as 0, 10\\u00a0min, 20\\u00a0min and 30\\u00a0min respectively. The treated perovskite films for characterization were prepared by removing gold and Spiro-OMeTAD with tape and chlorobenzene respectively unless otherwise stated.\\n\\nTheoretical calculations for the treated perovskite materials were performed using density functional theory (DFT) within generalized gradient approximation of the Perdew-Burke-Ernzerh functional, as implemented in the Vienna ab initio simulation package (VASP) []. All the structures of the compounds in this work were fully relaxed until energy and force converged to 10\\u22125\\u00a0eV and 0.001\\u00a0eV\\u00a0\\u00c5\\u22121, respectively. Long range van der Waals dispersion was also considered in this calculation by using empirical correction in Grimme's scheme []. For the lattice relaxation, we choose the most stable cell with orthorhombic Pnma spacegroup. A 3\\u00a0\\u00d7\\u00a03\\u00a0\\u00d7\\u00a03 Monkhorse-pace mesh was chosen for k-sampling of the Brillouin zone. For the Ab initio molecular dynamics (AIMD) simulation, a 2\\u00a0\\u00d7\\u00a01\\u00a0\\u00d7\\u00a02 supercell was used with canonical ensemble to evaluate the thermodynamic stability of the material. Each time step was set to 1.0 fs, and simulations were conducted for 5\\u00a0ps\\u00a0at 400\\u00a0K.\\n\\nX-ray diffraction pattern (XRD, Rigaku Smartlab) of the perovskite films deposited on FTO glass substrates was obtained with an XRD facility with monochromatic CuK\\u03b1 (\\u03bb\\u00a0=\\u00a00.154\\u00a0nm) excitation source at a scan rate of 1.5\\u00b0 min\\u22121 and step size of 0.02\\u00b0. The morphology of the thin film samples was measured using a field emission scanning electron microscope (FESEM, Joel 7001F) at an acceleration voltage of 5\\u00a0kV. The powder samples were diluted in chlorobenzene to obtain their transmission electron microscopy (TEM, Joel 2100). First Ten Angstroms dynamic contact angle analyser (FTA 200) was employed to measure the water contact angles and evaluate the hydrophobicity of the perovskite and perovskite/spiro-OMeTAD surface at room temperature (25\\u00a0\\u00b0C). Ultraviolet photoelectron spectra (UPS, HeI as resonance line, photo energy 21.22\\u00a0eV) were measured through Kratos AXIS Supra photoelectron spectrometer. Ultraviolet\\u2013visible absorbance spectrum of the samples was detected by Cary 50 UV\\u2013visible spectrometer. Steady-state fluorescence emission spectra of the samples were measured by a fluorescence spectrophotometer (Cary Eclipse) with excitation at 475\\u00a0nm wavelength. Time-resolved photoluminescence (TRPL) was tested by a fluorescence spectrophotometer (FLSP-900, Edinburgh Instrument) with a 377\\u00a0nm pulsed diode laser excitation source. The obtained data were analysed following a bi-exponential equation bellow. I(t)=A1exp(\\u2212t\\u03c41)+A2exp(\\u2212t\\u03c42)+A0\\nThe current-voltage (J-V) plots of perovskite solar cells was tested under irradiation of 100\\u00a0mW\\u00a0cm\\u22122 (AM 1.5, 1 sun) through a solar simulator (Oriel Sol3A, Newport) equipped with 450\\u00a0W Xenon lamp. The controlled active area of the device was 0.115\\u00a0cm2 with a black mask to avoid scattered light. The scan rate in the J-V measurement was 100\\u00a0mV\\u00a0s\\u22121. No preconditioning such as light soaking or voltage bias was applied with the devices. Space-charge-limited current (SCLC) of the electron-only devices was measured in the dark with a digital source meter (Keithley 2400, SMU Instrument). Incident photon-to-electron conversion efficiency (IPCE) system (EQE/IQE 200B, Newport) under AC mode was used to measure the external quantum efficiency (EQE) of the PSCs. Impedance spectroscopy (IS) was performed with the devices under open-circuit voltage condition in a frequency range from 1\\u00a0MHz to 0.1\\u00a0Hz by an electrochemcial workstation (BioLogic) under different illumination intensities controlled by neutral density optical filters. The J-V plots of the solar cells under different light intensity were also measured to obtain relationship of V oc vs illumination intensity. The stability of device performance against high humidity was monitored by periodically measuring the J-V plots of PSCs without encapsulation stored in a custom-built humidity-controlled chamber (relative humidity> 65% for 968\\u00a0h (~40 days).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.5I2.5,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: E-beam evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25; 25,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: 17.2,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.115,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The ink preparation procedures for GNF and the 2H-MoS2 flakes, by liquid phase exfoliation of graphite and bulk MoS2 respectively, and have been prepared according to a previously described procedure . For the buffer layer deposition, 150\\u00a0\\u03bcL of the 2H-MoS2 ink is spin-coated onto the perovskite layer at 2000\\u00a0rpm for 20\\u00a0s. The morphology of the buffer layer has been already studied elsewhere . Steady-state photoluminescence (PL) measurements are performed with a commercial apparatus (Arkeo \\u2013 Cicci Research s.r.l.) composed by a 0.3\\u00a0m focal length spectrograph with a photon counting unit. The substrates are excited by a green (532\\u00a0nm) laser at 45\\u00b0 of incidence with a circular spot diameter of 1\\u00a0mm. The optical coupling system is composed by a lens condenser and a long pass filter.\\n\\nPatterned F-doped tin oxide (FTO) coated glasses are first washed with a liquid detergent dissolved in deionized water and then cleaned by ultrasonic bath with acetone and IPA for 10\\u00a0min. The compact TiO2 blocking layer (c-TiO2) is deposited by spray pyrolysis with a solution of acetylacetone (2\\u00a0mL), titanium diisopropoxide (3\\u00a0mL) and ethanol (45\\u00a0mL) at 480\\u00a0\\u00b0C. In the ref-PSC, the c-TiO2/FTO substrate is coated by a thin m-TiO2 porous film (\\u223c150\\u00a0nm) deposited by spin coating a TiO2 paste (Dyesol 18 NR-T paste diluted in ethanol 1:5 in wt.) at 4000\\u00a0rpm for 20\\u00a0s. The graphene doped m-TiO2 is produced by adding 1% v/v of graphene ink to TiO2 diluted paste. The subsequent sintering at 480\\u00a0\\u00b0C for 30\\u00a0min is performed in air. The CH3NH3PbI3 layer is deposited onto mesoscopic TiO2 by the sequential deposition of PbI2 (500\\u00a0g\\u00b7L\\u22121, in dimethylformamide) and CH3NH3I (10\\u00a0g\\u00b7L\\u22121 in IPA) in a nitrogen filled glovebox system. The supersaturated PbI2 solution is first deposited by spin coating at 6000\\u00a0rpm for 10\\u00a0s and then directly dipped into the CH3NH3I solution for 15\\u00a0min. During the second step theCH3NH3PbI3 layer formation is completed by annealing at 80\\u00a0\\u00b0C and by rinsing with anhydrous IPA. Then, the 2H-MoS2 flakes in IPA and spiro-OMeTAD (73.5\\u00a0g\\u00b7L\\u22121 in chlorobenzene solution doped with TBP (26.77\\u00a0\\u03bcL\\u00b7mL\\u22121), LiTFSI (16.6\\u00a0\\u03bcL\\u00b7mL\\u22121) and a Cobalt (III) FK209 complex (7.2\\u00a0\\u03bcL\\u00b7mL\\u22121)) are sequentially deposited by spin coating at 2000\\u00a0rpm for 20\\u00a0s in a glovebox. Finally, the device was completed by the HV thermal evaporation of a gold counter electrode (100\\u00a0nm) on an active area of 0.1\\u00a0cm2 defined by a shadow mask. The devices were encapsulated with a glass lid sealed on the device only on the substrate edge.\\n\\nCurrent density-voltage (J-V) characteristics of PSCs are measured under simulated AM 1.5\\u00a0G solar light at 1000\\u00a0W\\u00b7m\\u22122 irradiance generated by a solar simulator (ABET Sun 2000, class A). The system is calibrated with a certified reference Si Cell (RERA Solutions RR-1002) and devices are measured using a mask to define the active area. A modular testing platform (Arkeo-Cicci research s.r.l.) is employed to perform transient photo-voltage (TPV), stability at the maximum power point (MPP) and to determine the VOC and JSC dependence from the illumination intensity. The system is equipped with a white LED array (4200\\u00a0K) tuneable up to the optical power density of 2000\\u00a0W\\u00a0m\\u22122 and with a high-speed source-meter unit. The set-up allows measuring up to four devices in parallel. High perturbation TPV tests allow recording VOC decay and rise profiles by switching the light intensity from dark to 1 SUN (1000\\u00a0W\\u00b7m\\u22122) (for more details, see reference39). The aging test under prolonged sun irradiation is realized by employing a high-power white LED (Bridgelux \\u2013 50C10K0 @5000\\u00a0K) calibrated at 1 SUN in ambient atmosphere and temperature. A Perturb&Observe algorithm is used to track the MPP trend with a refresh time of 1\\u00a0s, while a new I\\u2013V scan is recorded under LED illumination every 20\\u00a0min. During the 24\\u00a0h light-soaking aging test, the temperature was retained constant at room temperature by a water-refrigerated stage.\\n\\nFor the XPS depth profile analysis (K-Alpha, Thermo Scientific), glass-sealed solar cells were stored in inert ambient for 48\\u00a0h after the fabrication in the case of reference devices or subjected to light-soaking-aging test. After the glass lid encapsulation removal, the devices were analyzed by alternating ion sputtering with low-energy (500\\u00a0eV) Ar+ beam and XPS analysis performed in the \\u201csnapshot\\u201d mode with a monochromatic Al K\\u03b1 X-ray beam with a spot size (analysis area) of 200\\u00a0\\u03bcm and a raster area of 1\\u00a0mm. The snapshot mode allows acquiring single spectra (C 1s, O 1s, Au 4f, Pb 4f, I 3d and Sn 3d) with a good energy resolution and signal-to-noise ratio in only a few minutes. The atomic percentages are evaluated at each profile step by peak fitting using Avantage software after Shirley background subtraction. ToF-SIMS 3D imaging was performed with a dual beam ToF-SIMS (TOFSIMS IV from Ion-TOF GmbH, M\\u00fcnster, Germany) spectrometer equipped with a 25\\u00a0keV Bi3 + beam for the analysis and a 500\\u00a0eV Cs+ ion beam for the sputtering operated in the non-interlaced bunched mode. These conditions allow for an in-plane resolution of \\u223c1\\u00a0\\u03bcm, an in-depth resolution of \\u223c1\\u00a0nm and a mass resolution M/\\u0394M of \\u223c5000. ToF-SIMS profiles are built by selecting the most relevant molecular ions in the mass spectra (0\\u00a0<\\u00a0m/z\\u00a0<\\u00a0800) and displaying their evolution as a function of the sputtering time. The sputtering time can't be directly translated into a depth (z direction) because of the variable sputtering rate when profiling soft (organic) and hard (inorganic) layers. Profiles have been repeated twice on as prepared and aged device for all PSC architectures.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | Graphene,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 80.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 15.0,\\n HTL_stack_sequence: 2H-MoS2 | Spiro-MeOTAD,\\n HTL_additives_compounds: Unknown | FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Ambient,\\n Stability_time_total_exposure: 24,\\n Stability_PCE_initial_value: 15.8,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All reagents were used as received without further purification, including PbI2 (99.999%, Sigma-Aldrich), isopropanol (99.99%, Sigma-Aldrich), Aminomethane (CP Beijing Chemical Works), Spiro-OMeTAD (Lumtec), N,N-dimethylformamide (99.99%, Sigma-Aldrich), ethanol (AR Beijing Chemical Works), HI (57%, Alfa Aesar), TiAc2 (75 wt% in isopropanol, Sigma-Aldrich), Cs2CO3 (99.9%, Sinopharm Chemical Reagent Co.,Ltd), octadecene (ODE, 90%, Sigma-Aldrich), oleic acid (OA, 90%, Sigma-Aldrich), PbBr2 (99.999%, Aladdin Industrial Corporation), oleylamine (OLA, 90%, Sigma-Aldrich), hexane (99.9%, CP Beijing Chemical Works), toluene (CP Beijing Chemical Works), 4-tert-butylpyridine (99.9%, SigmaAldrich), chlorobenzene (99.9%, Sigma-Aldrich), acetonitrile (99.9%, Sigma-Aldrich), and ITO substrates.\\nThe CH3NH3I was prepared according to the reported procedure . And TiO2 nanoparticles were synthesized following a previously method .\\n\\nIn a typical synthetic experiment, a mixture of 0.4 g Cs2CO3, 1.2 mL OA and 15 mL ODE was loaded into 100 mL three-neck flask, dried for 1 h at 120 \\u00b0C, and then heated under N2 to 150 \\u00b0C until all Cs2CO3 reacted with OA to form Cs-oleate solution. The Cs-oleate has to be pre-heated to 100 \\u00b0C because it will precipitate out of ODE at room temperature. Then 0.3 mmol PbBr2 and 8.3 mL ODE were loaded into a 50 mL three-neck flask and heated under vacuum for 1 h at 120 \\u00b0C. 0.67 mL dried OA and 0.5 mL dried OLA were injected into the PbBr2 solution at 120 \\u00b0C under N2. The temperature was raised to 150 \\u00b0C allowed for complete dissolution of the PbBr2 salt. After that, 1 mL as-prepared Cs-oleate solution was quickly injected into the above solution and hold at 150 \\u00b0C for another 10 min, then, the reaction mixture was cooled by an ice-water bath. The aggregated CsPbBr3 nanowire composites were separated by centrifugation at 6000 rpm for 10 min and washed twice with hexane. Finally, different CsPbBr3 were dispersed in toluene which was used for the subsequent experiment.\\n\\nA 40 nm thick layer of TiO2 nanoparticle (TiAc2 stabilized) in ethanol was spin-coated on an ITO substrate, which was washed by distilled water, anhydrous ethanol, acetone and isopropanol sequentially. The TiO2 transport layer was then annealed at 150 \\u00b0C for 30 min in atmosphere. For the SnO2 based solar cell, the SnO2 transport layer was deposited on the ITO substrate by spin-coating the SnCl2 solution, and then was annealed at 180 \\u00b0C for 30 min . Later, the MAPbI3(Cl) film was deposited by sequential solution procedure. For instance, 450 mg PbI2 dissolved in 1 mL DMF, was spin-coated on the ETL substrate at 3000 rpm for 30 s (6500 rpm/s) and then annealed at 70 \\u00b0C for 20 min. After PbI2 cooling to room temperature (25 \\u00b0C), CH3NH3I(Cl) solution (50 mg CH3NH3I and 5 mg CH3NH3Cl was dissolved in 1 mL isopropanol) was spin-coated on the PbI2 substrate at 3000 rpm for 30 s (6500 rpm/s), and then the MAPbI3(Cl) film was annealed at 150 \\u00b0C for 15 min in atmosphere. For the optimized perovskite solar cell in the present work, 40 \\u03bcL as-prepared CsPbBr3 in toluene (1 mg/mL) was deposited on the MAPbI3(Cl) by spin-coating at 3000 rpm for 60 s, and then annealed at 70 \\u00b0C for 1 min. After that, the hole transport layer (HTL) solution was spin-coated at 3000 rpm for 30 s, which was prepared by dissolving 17.5 mL of a stock solution of 520 mg/mL lithium bis(trifluoromethylsulphonyl)imide, 72.3 mg Spiro-MeOTAD and 28.8 mL tBP in acetonitrile in 1 mL chlorobenzene. Finally, 100 nm gold as counter electrode was deposited by thermal evaporation under a pressure of 5 \\u00d7 10\\u22125 Torr using a shadow mask to pattern the electrodes. For the semitransparent perovskite solar cell, 5 nm thick MoOx layer, 1 nm thick Au layer, 10 nm thick Ag layer and 20 nm thick MoOx layer was deposited sequentially by thermal evaporation on the HTL. The evaporation rates for each layer are 0.04, 0.02, 0.4 and 0.04 nm/s, respectively. The active area of solar cell in this work was 0.15 cm 2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70 >> 150,\\n Perovskite_deposition_thermal_annealing_time: 20.0 >> 15.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 400,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 75,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The crystal growth of the RbPbI3 perovskite was prepared by a fusion method via available the literature . To grow the RbPbI3 single crystal, we mixed RbI and PbI2 at a stoichiometric ratio and placed these materials in a Pyrex tube which was then sealed in a low vacuum state (1 \\u00d7 10-6 Torr). Heating to 800 oC followed, at which the samples were sufficiently melted. After maintaining a temperature of 800 oC for 5 h, the samples were cooled slowly from 800 \\u00b0C to 40 \\u00b0C over a time period of 100 h, allowing the formation of crystal nuclei with the subsequent formation of a larger crystal due to the attachment of other crystals on the surface of the crystal nuclei.\\n\\nThe RbPbI3 solar cell was fabricated with a FTO substrate 2 cm \\u00d7 2 cm in size. The devices were illuminated through a shadow mask, yielding an active area of 0.175 cm2. To fabricate the solar cell, a 50 nm compact layer of TiO2 was deposited on the FTO substrate by spin coating (2000 rpm 30 s) a mildly acidic solution of titanium isopropoxide (TTIP) in ethanol containing 350 \\u03bcL TTIP in 5 mL EtOH containing 0.013 M HCl. Then we conducted the annealing process at 550 \\u00b0C for 30 min. A mesoporous TiO2 layer, which was prepared diluted TiO2 paste (DYESOL-18NRT) with ethanol with a ratio of 1:3.5 w/w, was spin-coated on the TiO2 compact layer at 500 rpm for 5 s, 3000 rpm for 10 s and 6000 rpm for 30 s and then, sintered at 550 \\u00b0C for 30 min. To interconnected TiO2 layer, the substrate was further treated with 20 mM TiCl4 aqueous solution at 70 oC for 30 min, rinsed with deionized water and ethanol, and then annealed at 500 \\u00b0C for 30 min. The equimolar 1 M RbI and PbI2 were dissolved in the DMF solvent. The solution was spin coated on the N type TiO2 layer at 4000 rpm for 30 s followed by the annealing process at 100 oC for 30 min. A solution for spiroMeOTAD coating was prepared by dissolving 72.3 mg spiroMeOTAD in 1 mL of chlorobenzene, to which 28.8 \\u03bcL of 4-tert- butyl pyridine (TBP) and 17.5 \\u03bcL of lithium bis(trifl uoromethanesulfonyl) imide solution (520 mg Li-TSFI in 1 mL acetonitrile (Sigma\\u2013Aldrich, 99.8%)) were added . Spiro-MeOTAD was deposited at 4000 rpm for 30 s on the perovskite layer. The gold layer of 800 \\u00c5 for the counter electrode was deposited on the perovskite layer with the thermal evaporation at 1.5 \\u00c5/s.\\n\\nOptical diffuse reflectance measurements were performed at room temperature using a Cary 5000 (Varian) spectrometer operating in a wavelength range of 175\\u20133300 nm. The diffuse reflectance measurement was used to estimate the band gap of the material by converting reflectance to absorption data according to the Kubelka\\u2013Munk equation : \\u03b1/S = (1\\u2013R)2(2R)\\u22121, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. More than 20 solar cells were measured using simulated solar light of AM 1.5 G produced by a 1000 W xenon lamp (Oriel, 91193). Its irradiance was calibrated with a Si reference solar cell (NREL certified KG5 filtered silicon reference diode) to adjust the one sun light intensity (100 mW/cm2). The emission and exciton spectrum of RbPbI3 were measured with a FluoroMate FS-2 \\u2013 Fluorescence Spectrometer (Scinco, Republic of Korea). Hall effect measurements were conducted in air using four contacts The Hall bar method utilized DC current flowing through perovskite film applied using a Keithley Model 2400 instrument, and the Hall voltage was recorded using a Keithley Model 4200. Field strength of 0\\u20131.25 T and current of 100 nA were applied. The observed voltage was 0.19\\u20130.25 V. and the calculated resistivity was 8.48 \\u00d7 104\\u20131.10 \\u00d7 105 \\u03a9 cm.\\nThe intensity modulated photovoltage spectroscopy (IMVS) and intensity modulated photocurrent spectroscopy (IMPS) measurements were performed on a ZAHNER CIMPS system (ZAHNER-elektrik GmbH & Co.). The LED was operated with a potentiostatic feedback loop to control the stationary DC voltage and a concurrent sinusoidal modulated AC voltage. The AC amplitude was fixed at 10% of the stationary DC value. The solar cell was placed under the potentiostat unit. IMPS measured the periodic photocurrent response of the cell to the variation of light intensity, while the IMVS experiment was used to measure the periodic modulation of the photovoltage under the change of light intensity modulation. The real and imaginary part of the modulated photovoltage and photocurrent of the IMVS and IMPS were calculated with the Levenberg-Marquardt algorithm program. Mott-Schottky (C-2\\u2013 \\u03d5) analysis (Garmy instrument) was measured at a frequency of 100 Hz from \\u22121 to 1 V with a 0.1 V voltage step. Ultraviolet photoemission spectroscopy (UPS, model AXIS-NOVA, Kratos) spectra of the ITO surface were studied to determine HOMO level and work function of RbPbI3 in an ultrahigh vacuum (UHV). The base pressure of the chamber was 2 \\u00d7 10\\u221210 Torr, which rose to 5 \\u00d7 10\\u22126 Torr during the Ar-ion sputtering due to Ar-gas backfilling. During the UPS measurement the pressure went to the high 10\\u22129 Torr range mainly due to the He. The He I line at 21.2 eV was taken as the excitation source for the UPS. The X-ray source was the Al K\\u03b1 line at 1478 eV. The optical constant of RbPbI3 thin film was measured at room temperature and low humidity (< 25% RH) by the VASE-ellipsometer (J. A. Woollam Co., Inc).\\n\\nThe RbPbI3 crystal was coated with Paratone-N oil (Paratone-N oil was used not only for mounting on a dual-thickness MicroLoop Ld assembly (MiTeGen, USA) but also to protect the crystal from a cold nitrogen stream at 100 K. Paratone-N oil is also stable 298 K and 450 K, and protection from the nitrogen stream was accomplished using a Cryojet-5 device (Oxford Instrument Inc.; temperature range 85\\u2013500 K)) and the diffraction data was measured at 100 K, 298 K, and 450 K with synchrotron radiation (\\u03bb = 0.61000 \\u00c5) on a ADSC Quantum-210 detector at BL2D SMC with a silicon (111) double crystal monochromator (DCM) at the Pohang Accelerator Laboratory Korea. The PAL BL2D-SMDC program was used for data collection (detector distance 63 mm, omega scan; \\u2206\\u03c9 = 3\\u00b0, exposure time 1 s per frame), and the HKL3000sm (Ver. 703r) was used for cell refinement, reduction, and absorption correction. The crystal structure of the RbPbI3 was solved by the direct method with the SHELXT-2014 program and refined by full-matrix least-squares calculations with the SHELXL-2014 program package .\\n\\nThe calculations of DFT were done using a highly precise full-potential linearized augmented plane wave (FLAPW) method with local density approximation (LDA) for the exchange-correlation potential. Muffin-tin radii of 3.0 a.u. (Rb), 2.50 a.u. (Sn and Pb), and 2.35 a.u. (I) were used with cutoffs for basis expansion and charge, potential representation of 14.82 and 144 Ry, respectively. Summation in reciprocal space was performed with 20 k points in the irreducible wedge. All atomic positions were fully relaxed with a force criteria of 1 \\u00d7 10-3 eV/\\u00c5. The convergence criteria in our calculations are 10-4 htr/(a.u.)3 in all cases; the difference in the charge density for two successive iterations is less than that value. There are two means of determining the convergence criteria: (i) the charge density difference, and (ii) the total energy difference between two successive iteration steps, with the former depending on how we established the charge density criteria. As the systems are all insulators, that would be sufficient. Additional information was already given in the \\u201cComputational Methods\\u201d section, where we discuss the use of the full-potential linearized augmented plane wave (FLAPW) method.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | TiCl4,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: RbPbI3,\\n Perovskite_composition_short_form: RbPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1440,\\n Stability_PCE_initial_value: 1.02,\\n Stability_PCE_end_of_experiment: 98,\\n Cell_area_measured: 0.175,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were used as received without any further purification. Copper(I) thiocyanate (CuSCN, 99%) and SnCl2 (>99%) were purchased from Sigma-Aldrich. CH(NH2)2I was purchased from Dyesol Ltd. SnI2 (99.999%) and phenyl-C71-butyric acid methyl ester (PCBM) were purchased from Alfa Aesar and Nano-C, respectively.\\n\\nThe ITO-coated glass substrates were cleaned via ultrasonication in deionized water, acetone and isopropanol for 10 min, respectively. The process of preparing CuSCN on ITO was similar to previous reports. CuSCN dissolved in aqueous ammonia (10 mg mL\\u22121) was spin-coated on the ITO substrate at 4000 rpm for 20 s in ambient air and then the films were annealed at 150 \\u00b0C for 20 min on a hotplate in air. Then the films were transferred to a nitrogen-purged glovebox for later experiments. The FASnI3 perovskite precursor solution was prepared by dissolving 1 mmol SnI2 and 1 mmol FAI with 10 mol% SnCl2 in 1 mL mixed solvent (DMF:DMSO = 4:1). For the AHP included perovskite precursor solution, the molar ratio of AHP and SnI2 was 3%, 5% and 7%, respectively. The perovskite precursor solution was spin-coated on the CuSCN layer at 2000 rpm for 5 s and then at 5000 rpm for 30 s, and 100 \\u03bcL chlorobenzene was dripped onto the perovskite film at the 11th s. The obtained films were annealed at 70 \\u00b0C for 10 min. PCBM (20 mg mL\\u22121 in chlorobenzene) was spin-coated on the perovskite film at 1500 rpm for 30 s to function as an electron transporting layer. Finally, 90 nm silver electrodes were thermally evaporated on the PCBM layer under vacuum to complete the device fabrication. An active area of 0.048 cm2 was defined by a shadow mask.\\n\\nThe morphology of the films was recorded using a field-emission scanning electron microscope (Hitachi S-4300). The optical absorption spectra of perovskite films were measured using a Shimadzu UV-2550 spectrophotometer. XRD patterns were measured using a Rigaku SmartLab X-ray diffractometer using Cu K\\u03b1 radiation. The time-resolved photoluminescence (PL) spectra were obtained at 850 nm with an excitation of 650 nm using an FLS980 fluorescence spectrometer (Edinburgh Instruments, England).\\nThe current\\u2013voltage (J\\u2013V) curves of the solar cells were measured using a Keithley 2400 digital source meter under simulated air mass 1.5 G sunlight (Newport 91160, 300 W). The light intensity was calibrated using a standard monocrystalline silicon photodiode. EQE spectra were recorded on an Oriel integrated system. The Nyquist plots were recorded on a Zennium X electrochemical workstation (Zahner, Germany).\\nAll the measurements of PSCs were carried out in ambient air at room temperature without encapsulation. For the stability test, samples were stored in a N2 filled glovebox or under ambient conditions (\\u223c20% relative humidity) after measurements.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FASnI3,\\n Perovskite_composition_short_form: FASnI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: CuSCN,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 100,\\n Stability_PCE_initial_value: 2.34,\\n Stability_PCE_end_of_experiment: 50,\\n Cell_area_measured: 0.048,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Nickel acetate tetrahydrate (Ni(OAc)2\\u00b74H2O) and poly(bis(4-phenyl)(2,4,6-trimethylphenyl)amine) (PTAA) were obtained from Sigma-Aldrich and 1-Material, respectively. Methylammonium iodide (MAI) and PbI2 were purchased from Dyesol and TCI, respectively. Bathocuproine (BCP) and PCBM were acquired from Lumtec and Nano-C, respectively. All solvents were purchased from Sigma-Aldrich.\\n\\nThe process for fabricating the MAPbI3 perovskite precursor and films was exactly the same as that described in the previous work. Mixed perovskite Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3, narrow-bandgap perovskite Cs0.05FA0.95PbI3, and WBG perovskite Cs0.05(FA0.83MA0.17)0.95Pb(I0.6Br0.4)3 were fabricated via a one-step method reported elsewhere. The 0.1 M sol\\u2013gel NiOx precursor as a HTL was prepared by dissolving 24.88 mg of nickel acetate tetrahydrate and 6 \\u03bcL of ethanolamine in 1 mL of ethanol, and then stirring at 65 \\u00b0C for 2 h. The sol\\u2013gel NiOx was deposited onto a cleaned indium\\u2013tin-oxide (ITO) substrate by spin coating at 4000 rpm for 35 s; the coated substrate was then annealed at 120 \\u00b0C for 10 min and then at 280 \\u00b0C for 60 min. Another HTL of PTAA with a concentration of 2 mg mL\\u22121 dissolved in toluene was spin-coated at 5000 rpm for 35 s and then annealed at 100 \\u00b0C for 10 min. The fully dissolved MAPbI3 precursor was spin-coated onto the NiOx layer at 5000 rpm for 25 s, with 0.2 mL of chlorobenzene (CB) dropped 6\\u20137 s after the spin-coating process was started. The other mixed perovskite precursors were spin-coated onto the PTAA layer at 1000 rpm for 5 s and then at 5000 rpm for 20 s, with 0.2 mL of ethyl acetate (EA) dropped 10 s before the spin-coating process was ended.\\nAll of the as-fabricated films except CsFAPbI3 were subjected to solvent vapor annealing or thermal annealing at 100 \\u00b0C for 30 min. The CsFAPbI3 film was thermally annealed at 150 \\u00b0C for 30 min. In the solvent vapor annealing process, the perovskite films were placed on top of a hotplate and covered with a 100 mL glass Petri dish. Approximately 1 \\u03bcL of DMSO:water mixed solvent was added to the center of the Petri dish during the thermal annealing process so that the mixed vapor was well evaporated inside the Petri dish, ensuring that it contacted the perovskite layer. More details of the perovskite film fabrication methods are provided in the ESI.\\u2020 The PCBM solution was spin-coated onto the perovskite layer at 1000 rpm for 40 s, followed by annealing at 100 \\u00b0C for 20 min. The BCP solution was then spin-coated directly onto the PCBM layer at 4000 rpm for 35 s. The PCBM was dissolved in CB with a concentration of 20 mg mL\\u22121, and BCP was dissolved in ethanol with a concentration of 0.5 mg mL\\u22121. In the final step, a 100 nm-thick layer of Ag was thermally deposited onto the substrates as cathodes at a pressure less than 10\\u22126 Torr inside a vacuum thermal evaporator.\\n\\nGIWAXS measurements. 2D-GIWAXS measurements were performed at the PLS-II 5A beamline of the Pohang Accelerator Laboratory (PAL) in Korea. 2D-GIWAXS images were collected at 11.57 keV with a MAR charge coupled device (CCD) (sample-to-detector distance: 283.447 mm).\\nNEXAFS spectroscopy. Carbon K-edge NEXAFS measurements were conducted at the PLS-II 4D beamline of the PAL in Korea with a p-polarized photon beam. Angle-dependent NEXAFS spectra were recorded using several X-ray incidence angles of 30\\u00b0, 45\\u00b0, 55\\u00b0, and 70\\u00b0.\\n\\nThe J\\u2013V characteristics of the devices were measured using a Keithley 4200 source meter under AM 1.5G (100 mW cm\\u22122) light simulated using an Oriel solar simulator (Newport, class AAA solar simulator). The light intensity was calibrated using a Si solar cell certified by the National Renewable Energy Laboratory. The EQE was measured using an Oriel IQE-EQE 200B. The light intensity at each wavelength was calibrated with a standard single-crystal Si photovoltaic cell. All of the electrical tests were conducted in ambient air.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: NiO-c | PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: 16,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped tin oxide (FTO) glass (Solems) was etched with Zn powder and HCl (4 M). The substrates were sonicated for one hour in RBS\\u00ae detergent solution (2 vol%), rinsed with deionized water and ethanol, and then ultrasonicated in absolute ethanol, dried and heated at 500 \\u00b0C for cleaning. A TiO2 hole blocking layer was prepared by spray pyrolysis deposition (SPD) at 450 \\u00b0C employing a precursor solution made from 0.6 mL of titanium diisopropoxide bis(acetyl acetonate) (75% in 2-propanol, Sigma Aldrich) and 0.4 mL of acetyl acetone (Sigma Aldrich), employing 9 mL of absolute ethanol as a solvent and O2 as a carrier gas. The mesoporous TiO2 layer was prepared by spin-coating a solution of TiO2 paste (30 NR-D from Dyesol) in absolute ethanol (1:7 by weight) at 4000 rpm for 30 s. Subsequently, the films were sintered in a sequential heating process (5 min at 125 \\u00b0C, 5 min at 325 \\u00b0C, 5 min at 375 \\u00b0C, 15 min at 450 \\u00b0C and 30 min at 500 \\u00b0C). Then, the samples were transferred into a glovebox to continue the device preparation. MAPbI3 solution was prepared by mixing an equimolar concentration (1.42 M) of PbI2 (TCI Chemicals), methyl ammonium iodide (MAI, Dyesol) and DMSO (anhydrous) in DMF. The precursor solution was spin-coated onto the mesoporous TiO2 substrates and a few seconds later, washed by dripping 0.5 mL of anhydrous diethylether to induce the intermediate adduct formation of the films, as reported previously. Spiro-OMeTAD (2,2\\u2032,7,7\\u2032-tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9\\u2032-spirobifluorene) from Merck was employed as a hole transport material. 110 mg of Spiro-OMeTAD were dissolved in 1 mL of chlorobenzene containing tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) bis(trifluoromethylsulphonyl)imide (FK209, Dyesol), lithium bis(trifluoromethylsulphonyl)imide (LiTFSI, Sigma Aldrich) and 4-tert-butylpyridine (t-BP, Sigma Aldrich 96% of purity) as additives in relative molar concentrations of 5%, 50% and 330% respectively, with respect to Spiro-OMeTAD. Then, 35 \\u03bcL of that solution were deposited by spin coating at 3000 rpm for 20 s. Finally, 100 nm of gold was thermally evaporated under vacuum as the top contact of the solar cells.\\n\\nDevices were hermetically transferred to a Savannah 200 ALD system from Ultratech/Cambridge Nanotech, embedded into an MBraun glovebox, to deposit a ca. 16 nm-thick Al2O3 encapsulation layer. Trimethylaluminium (TMA, AlMe3, from Sigma Aldrich) and H2O were respectively used as Al and O precursors and kept at room temperature. Nitrogen (N2, 99.9999%, Air Liquide) was used as both carrier and purging gas. For encapsulation purposes, ALD cycles (H2O pulse/N2 purge/TMA pulse/N2 purge) with a typical time of 30 s were repeated 250 times (number of cycles) for a total run duration of approximately 2 hours with an average Growth Per Cycle (GPC) of \\u223c0.64 \\u00c5 per cycle for a final thickness of \\u223c16 nm. The deposition temperature was set at either 60 \\u00b0C or 90 \\u00b0C. Samples were taken out of the reactor right after the end of the run. For the devices containing the ALD-Al2O3 layer used for X-ray photoelectron spectroscopy (XPS) characterization, the number of cycles of that process was carefully reduced to prepare films only \\u223c2 nm thick. The glovebox with the Savannah system is located inside a cleanroom environment, so as to ensure a low level of particle contamination. Besides, the reactor contamination is particle-controlled so as not to add any particles to the thin film encapsulation process.\\n\\nThe reliability of the ALD-Al2O3 encapsulation process was evaluated by comparing the photovoltaic performance of PSCs before and after the ALD-Al2O3 step. PSC fabrication and characterization were done at IPVF whereas ALD-Al2O3 encapsulation was accomplished at CEA-LETI. Samples were shipped under an inert atmosphere from IPVF to CEA-LETI after an initial J\\u2013V characterization (before ALD-Al2O3 encapsulation) and shipped back to IPVF for further characterization (after ALD-Al2O3 encapsulation). To elucidate the origin of efficiency losses during the encapsulation process, reference PSC samples were fabricated and shipped together with the samples destined to be encapsulated. Accordingly, different kinds of reference samples were distinguished: reference samples with original efficiency or simply reference samples (coded as \\u201cRef\\u201d), samples shipped to CEA-LETI and stored inside a glovebox under a protecting N2 atmosphere (coded as \\u201cShipment\\u201d) and samples shipped to CEA-LETI and introduced inside the ALD reactor and heated under the same heating protocols used for the encapsulation process but without being exposed to ALD precursors/chemicals (coded as \\u201cH@T\\u201d). This way, we were able to discriminate the intrinsic degradation of PSCs (in Shipment) from the degradation related to the heating protocols of the ALD process (H@T) and the one associated with the combined effect of heating and ALD precursors (coded as \\u201cALD-Al2O3@T\\u201d). Long-term stability tests were performed by comparing the photovoltaic performances of the encapsulated devices and reference ones after long term storage (2256 hours, \\u223c94 days). For this, both ALD-Al2O3 encapsulated and reference samples were stored in a normal air atmosphere (no moisture or oxygen control, relative humidity around 80%) in a laboratory room to check environmental stability of the encapsulated devices vs. reference ones. The stability results are considered as the mean of four encapsulated solar cells.\\n\\nFor J\\u2013V characterization, an AAA sun simulator (Oriel Sol3A) with an AM1.5G spectrum (1 sun) was used as a light source. A digital source meter (Keithley Model 2400) was employed to realize a voltage sweep rate of \\u223c85 mV s\\u22121 (unless different conditions are explicitly specified) while the generated photocurrent of the solar cell was recorded. External quantum efficiency (EQE) measurements were acquired on an Oriel IQE200 system equipped with a source meter (Keithley 2400) using a digital lock-in amplifier (Oriel Merlin) without any additional light bias. For chronopotentiometry measurements, consecutive cycles of 30 minutes were carried out during 33.5 h. In this case, PSCs were kept at open circuit conditions with the help of a potentiostat (Autolab) under continuous illumination (0.65 Suns) also with an AM1.5G spectrum. Between cycles, the illumination was always turned on, but the voltage was set to 0 V before starting the next chronopotentiometry step to monitor the transient behavior before reaching VOC. The active area of the cells was 0.16 cm2 (4 \\u00d7 4 mm) while for J\\u2013V, EQE and chronopotentiometry measurements the illuminated area was fixed at 0.09 cm2 (3 \\u00d7 3 mm) with a metal black-painted mask.\\n\\nFor the time-resolved photoluminescence (TRPL) experiments, a monochromatic (\\u03bb = 532 nm) pulsed laser beam (TALISKER, Coherent) was used as a light source. The laser was coupled into a single-mode optical fibre connected to a homemade microscope to focus the light on the sample. The photoluminescence decay dynamics were recorded by time-correlated single-photon counting (TCSPC). An Aurea infrared single photon detector was coupled to a PicoHarp 300 for opto-electrical conversion of the decay signal to achieve a time resolution of 130 ps. The output signal was normalized and fitted between the peak of the pulse and the end of the signal using a biexponential model (see the ESI\\u2020).\\n\\nXPS measurements were performed on a K-Alpha+ (Thermo Fisher Scientific) spectrometer using a monochromatic Al-K\\u03b1 X-ray source (1486.6 eV). The spectrometer was calibrated using the Thermo Fisher Scientific K-Alpha+ procedure and verified on sputter-clean Cu and Au samples following the ASTM-E-902-94 standard procedure. High energy resolution peaks were acquired with a 400 \\u03bcm spot size with a Constant Analyser Energy mode of 20 eV and a 0.1 eV energy step size. No low-energy electron flood gun was necessary for the analysis. Quantification was performed based on the peak areas after a Shirley type background subtraction using a Thermo Fisher Scientific Avantage\\u00a9 data system.\\n\\nThe completed devices were observed by SEM with a Zeiss Merlin VP compact microscope.\\n\\nThe crystalline properties of the absorber were determined by XRD studies with a PanAnalytical Empyrean diffractometer using Cu-K\\u03b1 radiation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 2256,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 77,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned ITO-coated glass substrates (sheet resistance = 15 ohm sq\\u22121) were purchased from Ruilong Tech. PEDOT:PSS aqueous solution (CLEVIOS P VP Al 4083) was purchased from Heraeus. Methylammonium iodide (MAI; >99.5%) was purchased from Lumtec. PC61BM (>99.5%) was purchased from Solenne. P(NDI2OD-T2) was purchased from 1-Material Inc. N-DMBI (98%) was purchased from Sigma Aldrich. Unless otherwise stated, all chemicals were purchased from Sigma-Aldrich and used as received.\\n\\nMAPbI3 NWs were prepared according to the literature procedures with slight modification. A layer of MAPbI3 perovskite planar film was first formed through a standard two-step sequential deposition method. Briefly, PbI2 and MAI were dissolved into anhydrous dimethylformamide (DMF) and anhydrous 2-propanol with concentrations of 450 mg mL\\u22121 for PbI2 and 40 mg mL\\u22121 for MAI, respectively. Both solutions and substrates were heated at 100 \\u00b0C for 10 min before being used. The PbI2 solution was spun on the preheated substrate (5000 rpm for 40 s) and then annealed at 70 \\u00b0C for 10 min. The MAI solution was then spun on top of the dried PbI2 film (6000 rpm for 30 s), followed by annealing at 100 \\u00b0C for 2 hours. A mixed solvent (70 \\u03bcL DMF in 1 mL IPA) was then spin coated onto the perovskite thin film (4000 rpm for 30 s) and then annealed at 100 \\u00b0C for 5 min. The thickness of MAPbI3 NWs was \\u223c420 nm.\\n\\nITO-coated glass substrates were first ultrasonicated in detergent, deionized water, acetone and 2-propanol in turn, followed by UV-ozone treatment for 60 min. After filtration through a 0.45 \\u03bcm filter, the PEDOT:PSS layer (30 nm) was spin-coated on the cleaned ITO substrate at 4000 rpm for 60 s and then annealed at 120 \\u00b0C for 15 min. The substrates were then transferred to a nitrogen-filled glovebox. For the devices based on the planar film, the MAPbI3 perovskite layer (\\u223c350 nm) was prepared following two-step solution deposition, as described in our previous work. After the deposition of the perovskite layer, the solution of PC61BM (20 mg mL\\u22121 in chloroform) or P(NDI2OD-T2) solution (15 mg mL\\u22121 in 1,2-dichlorobenzene) with different doping ratios of N-DPBI was then spin-coated on top of the formed perovskite layers. The thickness of P(NDI2OD-T2) was 160 nm. Afterward, opaque Ag (150 nm) was deposited using a thermal evaporator under high vacuum (<10\\u22126 torr). The ALD Al2O3 film (50 nm) was prepared following our previous procedures. To eliminate the Jsc from regions outside the active area, illumination masks with aperture sizes of 0.12, 1.2, or 5.04 cm2 were used.\\n\\nA 100 nm thick Al2O3 gate dielectric was deposited by ALD at 200 \\u00b0C on a heavily doped p-type Si wafer that served as a back gate electrode. Afterward, the perovskite layer was deposited. Au metal contacts were subsequently deposited as the source/drain electrodes by thermal evaporation through a shadow mask. The channel length (L) and the channel width (W) were 60 \\u03bcm and 3500 \\u03bcm, respectively. Electrical characterization was carried out under vacuum using an Agilent 4156C semiconductor parameter analyzer. The field-effect mobility was extracted from the following equation in the saturation regime, ID = \\u03bcCi(W/2L)(VG \\u2212 VT), where ID is the drain current, \\u03bc is the field-effect mobility, W and L are the channel width and length, respectively, Ci is the capacitance per unit area of the gate dielectric, and VG is the gate voltage.\\n\\nThe device characteristics were evaluated under ambient conditions under an AM1.5G AAA class solar simulator (XES-100S1, SAN-EI Electric. Co. Ltd.) with an intensity of 100 mW cm\\u22122. A Hamamatsu silicon solar cell (S1133) with a KG5 color filter, which is traced to the National Renewable Energy Laboratory (NREL), was used as the reference cell. To calibrate the light intensity of the solar simulator, the power of the xenon lamp was adjusted to make the Jsc of the reference cell under simulated sunlight as high as it was under the calibration condition. The current density\\u2013voltage (J\\u2013V) curves were measured by using a Keithley digital source meter (Model 2400). Unless otherwise stated, the scan rate was set at 0.15 V s\\u22121. After initial measurements, the devices were kept under a controlled atmosphere using an indigenously made environmental control chamber. IPCE spectra were measured in DC mode using a lock-in amplifier with a current preamplifier under short-circuit conditions with illumination of monochromatic light from a 250 W quartz-halogen lamp (Osram) passing through a monochromator. Steady-state PL spectra were measured at room temperature by using a fluorescent spectrophotometer (Hitachi F-4600) with a 150W Xe lamp as an excitation source at 600 nm. Time-resolved PL decay spectra were recorded by using a time-correlated single-photon counting system (Edinburgh Instruments FL920), and the excitation light pulse was provided using a picosecond diode laser at a wavelength of 450 nm, and the signal was monitored at \\u223c760 nm. The PL lifetimes of the samples were calculated by fitting the experimental decay transient data to the double-exponential decay model. The surface morphology of the films was studied using tapping mode AFM using a Digital Instrument D3100CL. The electrical conductivities of the thin films were measured by using a four point probe setup with a source measurement unit (Keithley 2400). SEM was conducted with a field-emission SEM (S-4800, Hitachi) operated at an accelerating voltage of 10 kV with the samples coated with \\u223c3 nm of platinum. The XRD patterns were recorded using a multi-function high power X-ray diffractometer (Bruker D8 DISCOVER SSS) as the CuK source (wavelength = 1.541 \\u00c5). The film thicknesses were measured by using a Tencor Alpha-step surface profiler.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: P(NDI2OD-T2),\\n ETL_additives_compounds: N-DPBI,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA >> DMF; IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 100.0 >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> 10.0 >> 5.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 30.0; 30.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1500,\\n Stability_PCE_initial_value: 16,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 1.2,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A perovskite precursor solution was prepared by mixing BAI (99%, TCI), FAI (99%, MaterWin), PbI2 (99%, Alfa Aesar), and (NH2)2CS (99%, Sigma) with a molar ratio of 2:2:3:x (x = 0, 0.1, 0.25, 0.5, 0.75, 1, referred to as THA = 0, THA = 0.1, THA = 0.25, THA = 0.5, THA = 0.75, and THA = 1, respectively) in 1 mL of DMF (99%, Aldrich), and stirred overnight in a N2 glovebox at 70 \\u00b0C. Poly(3,4-ethylenedioxythiophene):poly(styrene-sulfonate) (PEDOT:PSS, PAI4083) aqueous solution was purchased from Baytron. (6,6)-Phenyl-C61-butyric acid methyl ester (PC61BM, 99.5%) was purchased from Lumtec. Bathocuproine (BCP, 99%) was purchased from J&K. Silver (Ag, 99.99%) was purchased from Alfa Aesar. All reagents and solvents were directly used without further purification, if not specified.\\n\\nITO-Coated glass (sheet resistance \\u226410 \\u03a9 cm\\u22122, MaterWin) was cleaned consecutively in detergent, acetone, isopropanol, and ethanol ultrasonic baths for 15 min, respectively. The ITO glass was treated with UV-Ozone for 15 min. A thin layer of PEDOT:PSS was spin-coated onto the cleaned ITO at 3000 rpm for 40 s, and annealed in a vacuum oven at 140 \\u00b0C for 25 min. Then the substrate was transferred into a glovebox for active layer deposition and further device fabrication. A perovskite active layer was spin-coated at 6000 rpm for 60 s onto the PEDOT:PSS coated ITO (ITO/PEDOT:PSS) substrate from 30 \\u03bcL of the perovskite precursor solution at a concentration of 1 M (based on PbI2), and annealed at 110 \\u00b0C for 15 min. After deposition of the perovskite active layer, PC61BM (20 mg mL\\u22121 in chlorobenzene) and BCP (0.5 mg mL\\u22121 in absolute ethanol) layers were deposited subsequently at 1500 rpm for 45 s and 3000 rpm for 30 s, respectively. The sample was then transferred into a vacuum chamber for further deposition of Ag (100 nm) to finish the device fabrication process. The device area is defined to be 0.06 cm2 using a metal mask, whereas the total device area defined by the overlap of the electrodes was approximately 0.12 cm2.\\n\\nThe chemical compositions of perovskite films before and after thermal annealing were compared using Fourier transform infrared (FTIR) spectra obtained on a Nicolet 5700 IR spectrometer (Thermo Fisher) under the diffuse reflectance mode with the signal of air as the calibration background. The crystallographic properties of (BA)2(FA)n\\u22121PbnI3n+1-based perovskite films were investigated using an Ultima IV diffractometer (Rigaku, graphite monochromatic, Cu-K\\u03b1 radiation) at room temperature with a scanning rate of 10\\u00b0 min\\u22121 over the Bragg angle range of 10.0\\u00b0\\u201350.0\\u00b0 (2\\u03b8). Film and device morphologies were studied using the scanning electron microscope (SEM) images obtained on an S-4800 field-emission scanning electron microscope (FESEM). Absorption spectra were recorded using a UV-2450 UV-visible spectrophotometer (Shimadzu). Grazing-incidence wide-angle X-ray scattering (GIWAXS) characterization of the 2D perovskite layer was performed at beamline 7.3.3, Advanced Light Source (ALS), Lawrence Berkeley National Lab (LBNL). The X-ray energy was 10 keV while operating in the top off mode. The scattering intensity was recorded on a 2D image plate (Pilatus 1M) with a pixel size of 172 mm (981 \\u00d7 1043 pixels). The sample-to-detector distance was about 300 mm. The incidence angle was chosen to be 0.6\\u00b0. The J\\u2013V characteristics were measured with Keithley 2400 measurement source units with the devices maintained at room temperature in the glovebox. The photovoltaic response was measured using a calibrated solar simulator (Enli Technology) at 100 mW cm\\u22122, and the light intensity was calibrated with a standard photovoltaic reference cell. The EQE spectrum was measured using a QE-R Model of Enli Technology. The (BA)2(FA)2Pb3I10-based perovskite films were kept in a humidity controlled cabinet (Hr = (55 \\u00b1 5%), Bossmen, PR1852(A)-SH) for humidity\\u2013stability measurements. The stabilities of the unsealed devices were tested under different conditions including a N2 atmosphere (glovebox) and air with Hr = 25 \\u00b1 5% and 55 \\u00b1 5%.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: BA2FA2Pb3I10,\\n Perovskite_composition_short_form: BAFAPbI,\\n Perovskite_additives_compounds: Thiourea,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 110,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 600,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 100,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Most of the reagents and solvents were purchased from Shanghai Aladdin Biological Technology Co., Ltd, including alcohol (99%), dimethyl formamide (DMF, \\u226599.9%), dimethyl sulfoxide (DMSO, \\u226599%), chlorobenzene (CB, 99.5%). The other reagents, like poly (3,4-ethylenedioxythiophene):poly (styrenesulphonate) (PEDOT:PSS, Clevios PVP AI 4083), CH3NH3I (MAI, 99%), PbI2 (99.99%), phenyl- C61-butyric acid methyl ester (PC61BM, 99.5%) and 4,7-diphenyl-1,10- phenanthroline (Bphen, 99%) were supplied by Xi'an Polymer Light Technology Corp. N2200 was purchased from Shanghai Han Feng Chemical Science and Technology Corp. (99.0%). All materials were used as received, without further purification.\\n\\nThe patterned indium tin oxide (ITO) glass substrates were cleaned sequentially in detergent, deionized water, absolute ethyl alcohol, acetone and isopropanol. Afterwards, the glass substrates were blown with N2 gas and then treated with a plasma cleaner for 5\\u202fmin. Next, PEDOT:PSS aqueous solution was filtered by a 0.45\\u202f\\u03bcm polyvinyl difluoride syringe filter and then spin-coated on the glass substrates at 6000\\u202frpm for 30\\u202fs, following annealing treatment on a hot plate at 125\\u202f\\u00b0C for 15\\u202fmin in air. Subsequently, the photoactive perovskite layer was spin-coated on the PEDOT:PSS substrates under nitrogen ambient (O2\\u202f\\u2264\\u202f0.1\\u202fppm; H2O\\u202f\\u2264\\u202f0.1\\u202fppm) by one step []. Further, N2200 dissolved in chlorobenzene with variable ratio (0, 0.5, 1.0, 1.5, 2.0\\u202fmg/mL) was spun at 3000\\u202frpm for 30\\u202fs in the glovebox, following annealing at 100\\u202f\\u00b0C for 5\\u202fmin. Then PC61BM (20\\u202fmg/mL, in chlorobenzene) was spun at 2700\\u202frpm for 30\\u202fs, subsequently, Bphen (0.7\\u202fmg/mL in anhydrous ethanol) as an interfacial layer was spun at 6000\\u202frpm for 30\\u202fs. Finally, 100\\u202fnm thickness silver film was deposited by vacuum thermal evaporation.\\nHere, the precursor solution of perovskite MAPbI3 was prepared by dissolving PbI2 and MAI with a molar ratio of 1:1.095 in the mixture solution of DMF and DMSO with a volume ratio of 9:1. During spin-coating the perovskite film, sec-butyl alcohol was added rapidly on the rotating perovskite film with a delay time of 7\\u22129s to prompt the fast crystallization of perovskite. The specific delay time mainly depends on the concentration of the perovskite precursor solution. After that, the formed films were transferred on a hot plate, first annealed at 105\\u202f\\u00b0C for 10\\u201320\\u202fmin in ambient air (real-time humidity of 30\\u223c50%) and then annealed at 105\\u202f\\u00b0C for 5\\u201315\\u202fmin in DMSO atmosphere. The solvent annealing time depends mainly on the humidity of the surrounding environment. Usually, the lower the humidity, the longer the annealing time.\\n\\nFilm thickness was measured with a stylus profiler (Dektak XT, Bruker). Surface morphology was analyzed using a scanning electron microscopy (SEM, Jeol JSM-7100F), and atomic force microscopy (AFM, Park Systems NX10). Steady-state and transient-state photoluminescence (PL) spectra were measured using a transient fluorescence spectrometer (FLS980, Edinburgh Instruments, E I). X-ray diffraction (XRD) was recorded using a Rigaku D/Max-B X-ray diffractometer. Fourier transform infrared spectrum (FTIR) was recorded by Thermo SCIENTIFIC infrared spectrometer (NICOLET iS10). Contact angle was analyzed using a contact angle tester (AST Optima). Current density-voltage (J-V) characteristics were measured using a Keithley 2400 source meter under a simulated AM 1.5G solar irradiation (100\\u202fmW\\u202fcm\\u22122) with a standard xenon-lamp-based solar simulator (ABET Sun 3000). And solar simulator illumination intensity was calibrated by a silicon reference cell calibrated by National Renewable Energy Laboratory (NREL). The active area of devices is defined as 0.04\\u202fcm2 by a black mask in J-V measurement. External quantum efficiency (EQE) was measured using a power source (Zolix Sirius-SS) with monochromator (Zolix Omni-\\u03bb). All measurements were performed in air environment without any encapsulation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: N2200 | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 105,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 200,\\n Stability_PCE_initial_value: 14.62,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The random copolymer P3TTA - co - P3HT was synthesized and characterized as reported in our previous paper []. In short 3-thiophene acetic acid (3-TAA, Sigma-Aldrich) was esterified with methanol and the protected monomer, 3-thiophene methyl acetate (3TMA, mole fraction n\\u202f=\\u202f0.5) were mixed with 3-hexyl thiophene (3-HT, n\\u202f=\\u202f0.5), in chloroform. It was then added slowly to the anhydrous ferric chloride solution of chloroform and was stirred in a two-necked round bottomed flask in N2 atmosphere at 0\\u202f\\u00b0C for 24\\u202fh. The monomer: oxidant ratio was kept 1:4. Then the P3TMA-co-P3HT was precipitated by adding methanol. The deprotection was performed by heating 0.5\\u202fg copolymer in 50\\u202fml NaOH solutions 2 (M) for 3 days and then the filtrate was collected. It was then neutralized with dilute HCl. The precipitate of P3TAA-co-P3HT was washed with deionized water followed by centrifugation and drying. The procedure of synthesizing the copolymer is summarized in Scheme 1 . The polymer has weight-average molecular weight (Mw) 21,800, PDI 2.69 and P3TAA content was 43\\u202fmol % producing almost an alternating copolymer configuration.\\n\\nMAI was prepared [] by mixing methylamine (40% in water, Spectrochem) with hydroiodic acid (HI, 57\\u202fwt %, Sigma-Aldrich) in a molar ratio 1.2:1\\u202fat 0\\u202f\\u00b0C under stirred condition. Water was removed after stirring for 2.5\\u202fh, using rotary evaporator at 60\\u202f\\u00b0C. It was washed with diethyl ether, recrystallized from ethanol, finally dried at 60\\u202f\\u00b0C in vacuum for one day.\\n\\nFluorine-doped tin oxide (FTO, Dyesol, TEC 8) was patterned by etching with Zn dust and concentrated HCl. It was washed successively in soap solution, deionized water, isopropanol, and acetone. A compact TiO2 film was prepared on the patterned FTO by spin coating of 0.2\\u202fM Ti(IV) bis(ethylacetoacetate)-diisopropoxide solution in n-butanol at 3000\\u202frpm for 45\\u202fs followed by thermal annealing at 450\\u202f\\u00b0C for 60\\u202fmin [,]. A mesoporous TiO2 layer was fabricated on the top of the compact layer by depositing diluted TiO2 in ethanol by spin coating at 3000\\u202frpm for 30\\u202fs. After drying at 150\\u202f\\u00b0C, the TiO2 films were heat-treated at 450\\u202f\\u00b0C for 45\\u202fmin and then cooled to room temperature. PVDF (Mw ~534,000, Aldrich) solutions of different concentrations e.g 0.25, 0.5, 1, 2.5, 5\\u202fmg/ml were prepared in anhydrous DMF and DMSO co-solvent (4:1 v/v), then 462\\u202fmg PbI2 and 50\\u202fmg MAI were added to the polymer solution. The solutions were stirred at 70\\u202f\\u00b0C for 8\\u202fh. The solution was spun cast on the top of the TiO2 film with a rotation speed of 3000\\u202frpm for 30\\u202fs. The PbI2/MAI films were heated at 100\\u202f\\u00b0C for 15\\u202fmin to crystallize the perovskite films.\\nA volume of 120\\u202f\\u03bcL of the synthesized P3TAA-co-P3HT solution in THF (15\\u202fmg/ml) was spin-coated onto the MAPbI3 perovskite layer at 4000\\u202frpm for 30\\u202fs to fabricate the hole transporting material (HTM). Ag contacts (100\\u202fnm) were deposited by evaporation to complete the devices at a vacuum of ~2\\u202f\\u00d7\\u202f10\\u22126\\u202fmbar. The active area of the PSCs was confined to be 0.22\\u202fcm2. The designation of different PVDF-perovskite hybrid PSCs produced adopting the above procedure are presented in Table 1 .\\n\\nMorphology of different hybrid PSCs were investigated with a scanning electron microscope (SEM, ZEISS EVO-MA 10). The structure of different PVDF-perovskite hybrids were investigated from X-ray diffraction data using X-ray diffractometer (Bruker AXS, model D8 Advance) fitted with a Lynx Eye detector and with Cu-K\\u03b1 radiation. The data were collected with a 0.05 step size (2\\u03b8). The absorption spectra were made at solid state on quartz plate with a UV\\u2013Vis spectrophotometer (model Cary 8454, Agilent). The fluorescence spectra of the solid films deposited on quartz surface was performed by a Fluoromax-3 instrument (Horiva Jovin Yvon).\\n\\nThe J\\u2013V characteristics curves of PSCs at ambient condition were recorded with a Keithley 2401 source meter. The cells were irradiated from a 150\\u202fW solar simulator fitted with an AM1.5G filter (Oriel Instruments) with calibrated intensity of 100\\u202fmW/cm2. The spectral dependence of the device for the incident photon to current conversion efficiency (IPCE) was measured by using a 150 Watt Xe-lamp in combination with a Newport monochromator (model CS130-USB-3-MC) and a Newport power source (Model No.67005). Electrochemical Impedance Spectra (EIS) were recorded with a Solartron SI1260 Impedance analyzer at 1\\u202fMHz to 0.1\\u202fHz frequency with open-circuit DC bias at 10\\u202fmV voltage perturbation. Preparation and characterization of the devices and electrical measurements were made under ambient condition (temperature 30\\u202f\\u00b0C, relative humidity 75\\u201385%).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: PVDF,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: P3TAA-co-P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 240,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 62,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All of the chemicals and materials were purchased and used as received unless otherwise noted. The fluorine doped tin oxide glass (FTO) was purchased from OPV Tech Co., Ltd. Lead iodide (PbI2) and methylamine iodine (MAI) were purchased from Xi'an Polymer Light Technology Corp. (PLT), and spiro-OMeTAD was purchased from Alfa. Ag (99.9%) was obtained from Aladdin. All liquid reagents such as dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF) and chlorobenzene (CB) were purchased from J & K Chemical Technology. The remaining reagents and materials related to perovskite solar cells were purchased from Sigma-Aldrich.\\n\\nIn the fabrication of the devices, fluorine doped tin oxide (FTO) was initially removed from regions under the anode contact by etching the surface with 2 M HCl and zinc powder. Then the substrate was cleaned with detergent/deionized water, acetone, and isopropanol. For the fabrication of electron selective layers (ESLs), a dense TiO2 (Den-TiO2) layer was spin-coated onto the pre-patterned FTO glass substrates at 3000 rpm for 30 s, with annealing at 450 \\u00b0C for 30 min. Subsequently, the mesoporous TiO2 (Mp-TiO2) was deposited by spin-coating at 5000 rpm for 30 s, and annealed at 500 \\u00b0C for 15 min. Then the perovskite layer was deposited, which would be induced later. Spiro-OMeTAD was introduced as a hole transport material (HTM) by spin-coating at 3500 rpm for 30 s. The solution of the HTM was prepared by adding 72.3 mg spiro-OMeTAD, 28.8 \\u03bcL 4-tert-butylpyridine (tBP), 17.5 \\u03bcL of a stock solution of 520 mg mL\\u22121 lithium bis-(trifluoromethyl sulphonyl) imide (Li-TFSI), and 20.0 \\u03bcL of a stock solution of 300 mg mL\\u22121 tris(1-(pyridin-2-yl)-1H-pyrazol) cobalt(III) tris(hexafluorophosphate) (FK102) in acetonitrile to 1 mL chlorobenzene. Finally, a 100 nm Ag electrode was deposited by thermal evaporation at 5 \\u00d7 10\\u22124 Pa on top of the device to form the back contact. The active area of these solar cells was 0.06 cm2 which was defined by a mask during the measurement. The perovskite film was sensitive to humidity, and thus, all procedures were performed under a N2 atmosphere.\\nFor MAPbI3 layer fabrication in M-PSCs, 462 mg mL\\u22121 PbI2N,N-dimethylformamide (DMF) was spin-coated onto the FTO/Den-TiO2/Mp-TiO2 substrate at 3000 rpm for 30 s. Furthermore, MAI dissolved in isopropanol was spin-coated onto the dried PbI2 layer at 5000 rpm for 30 s, and annealed at 125 \\u00b0C for 20 min.\\nFor MAPbI3 with spiro-OMeTAD additive fabrication in M-BHJ-PSCs: 462 mg PbI2 was added into different spiro-OMeTAD/DMF solutions to form PbI2/spiro-OMeTAD with different mass ratios. Then, 80 \\u03bcL of the above solution was spin-coated onto the FTO/Den-TiO2/Mp-TiO2 substrate at 3000 rpm for 30 s. Furthermore, MAI dissolved in isopropanol was spin-coated onto the dried PbI2 layer at 5000 rpm for 30 s, and annealed at 125 \\u00b0C for 20 min.\\nFor perovskite (MAPbI3\\u2212xClx) layer fabrication in planar PSCs: MAI and PbCl2 were diluted in anhydrous DMF at a 3:1 molar ratio of MAI to PbCl2 with a final concentration of \\u223c40 wt%. Then, the mixture was spin-coated on the FTO/Den-TiO2 substrate at 2000 rpm for 30 s, with annealing at 85 \\u00b0C for 1 h and 100 \\u00b0C for 25 min.\\nFor MAPbI3\\u2212xClx with spiro-OMeTAD additive fabrication in planar BHJ-PSCs: MAI and PbCl2 were diluted in anhydrous DMF at a 3:1 molar ratio for a final concentration of \\u223c40 wt%. Then, different mass ratios of spiro-OMeTAD/DMF additive were added into the precursor solution. The mixture was spin-coated on the FTO/Den-TiO2 substrate at 2000 rpm for 30 s, with annealing at 85 \\u00b0C for 1 h and 100 \\u00b0C for 25 min.\\n\\nA digital source meter Keithley 2460 (Keithley, USA) was used to measure the current density\\u2013voltage (J\\u2013V) curves of PSCs under simulated AM 1.5G (100 mW cm\\u22122, PEC-L15, Peccell, Japan). All the devices were measured with a 100 ms delay after a 10 mV voltage step, which is approximately equal to a scan rate of 0.1 V s\\u22121. A black mask (0.06 cm2) was used on top of the device to control the active light irradiation area of light irradiation. The incident photon-to-electron conversion efficiency (IPCE) was characterized from 365 nm to 1020 nm using a computer-controlled electrochemical workstation (Zen-nium Zahner, Germany). The top view and cross-section of the layers were investigated through field-emission scanning electron microscopy (Nova Nano SEM 450, FEI, USA). Electrochemical impedance spectroscopy (EIS) measurements were conducted on a computer-controlled electrochemical workstation (Zen-nium Zahner, Germany) under dark conditions. The measured frequencies ranged from 10 mHz to 4 MHz with 0.6 V bias voltage. The amplitude was 20 mV. TRPL spectra were taken with a Hitachi F-4500 fluorescence spectrometer. PL measurements were performed using an optically triggered streak camera system (C5410, Hamamatsu). All the samples were photoexcited using a 517 nm laser with a repetition rate of 76 MHz (Mira900, Coherent). Each of the samples was tested 3\\u20135 times, and the average data were obtained.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Spiro,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 125.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 20.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK102; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PEDOT:PSS aqueous solution (Clevis PVP Al 4083) with a concentration of 1.3\\u20131.7% by weight was purchased from Heraeus. Healy-C61-butyric acid methyl ester (PCBM, 99.5% purity) was acquired from Nano-C, Inc. Methylammonium iodide (MAI, >99.5% purity), PbI2(>99.99% purity), and PbCl2 (>99.99% purity) were supplied by Xi'an Polymer Light Technology Corp. Rhodamine 101 (RhB101) and other chemical solutions, such as isopropanol (IPA, 99.7% purity), \\u03b3-butyrolactone (GBL, >99% purity), and dimethyl sulphoxide (DMSO, >99.9% purity), were obtained from Sigma-Aldrich. All solvents were used directly without further purification.\\n\\nThe perovskite precursor solution with a composition of 0.14 M (39 mg) PbCl2, 1.26 M (581 mg) PbI2, and 1.3 M (209 mg) MAI was dissolved in a 1 ml co-solvent of DMSO:GBL (3:7 volume ratio) solution. The perovskite solutions were heated at 70 \\u00b0C for 12 hours inside a glove box filled with nitrogen gas.\\n\\nITO glass substrates (sheet resistance of 15 \\u03a9 \\u22121) were sequentially washed with detergent, deionized (DI) water, ethyl alcohol, acetone, and isopropanol (IPA) for 30 min. Then the ITO substrates were dried with nitrogen flow and treated under UV ozone for 30 min. The thin PEDOT:PSS layer was spin-coated on the clean patterned ITO glass substrates through a 0.45 micron Teflon filter at 8000 rpm for 40 s in an ambient atmosphere, and annealed at 120 \\u00b0C for 15 min to obtain the PEDOT:PSS HTL. After the PEDOT:PSS film was cooled down to room temperature, the substrates were moved into a glovebox filled with dried nitrogen (<1.0 ppm of O2 and H2O) for the deposition of perovskite films. 80 \\u03bcl of different concentrations of PTAA solution (0 mg ml\\u22121, 0.25 mg ml\\u22121, 0.5 mg ml\\u22121 and 0.75 mg ml\\u22121 toluene) were spin-cast on top of the PEDOT:PSS film at 8000 rpm for 40 s and annealed on a hot plate at 100 \\u00b0C for 3 min. After the films were cooled down to room temperature, the MAPbI3\\u2212xClx photoactive layer was then deposited by a simple one-step deposition method. The perovskite precursor solution (50 \\u03bcl) was spin-coated on the PEDOT:PSS films and PTAA-modified films at a rotational speed of 1000 rpm for 20 s and at 3500 rpm for another 40 s, and before the end of the spin coating process, 1 ml of methylbenzene was poured into the spinning film in a few seconds. Subsequently, the obtained perovskite films were placed on a heating table at 95 \\u00b0C for 5 min to form MAPbI3\\u2212xClx films. PCBM which had been dispersed in toluene with a concentration of 23 mg ml\\u22121 was spin-coated on top of the perovskite films at a rotational speed of 2500 rpm for 30 s. After this, the substrate was annealed at 100 \\u00b0C for 10 min. Then, the RhB101 layer was spin-coated on PCBM films at 1500 rpm for 40 s with a concentration of 0.6 mg ml\\u22121. Finally, the films were transferred to a thermal evaporation chamber under high vacuum (<2.5 \\u00d7 10\\u22125 Pa), and then a 1.2 nm LiF film and a 100 nm Ag film were sequentially deposited on PCBM through a shadow mask.\\n\\nX-ray diffraction (XRD) patterns were recorded using a PANalytical Empyrean diffractometer equipped with Cu K\\u03b1 radiation (\\u03bb = 1.5406 \\u00c5), at a step of 0.02\\u00b0 and a scan speed of 2.3\\u00b0 min\\u22121. Optical absorption spectra and transmission spectra were measured by using a UV-vis spectrophotometer (Shimadzu UV-1800). The steady-state photoluminescence (PL) spectra were obtained using a fluorescence spectrophotometer (Cary Eclipse, Agilent) with an excitation wavelength of 530 nm. The cross-section of the devices and the surface topography of the perovskite films were characterized using a JEOL JSM-7800F field emission scanning electron microscope (SEM). Atomic-force microscopy (AFM) was carried out using an MFP-3D-BIO AFM (Asylum Research, an Oxford Instruments company, USA). The time-resolved PL measurements were carried out using a combined fluorescence lifetime and steady-state spectrometer (FLS980, Edinburgh Instruments Ltd.) with a 510 nm picosecond pulsed laser. Photocurrent\\u2013voltage (I\\u2013V) curves were measured by using a Keithley 2400 source meter with an AM 1.5G solar simulator (Newport, 2612A) which was calibrated using a silicon reference cell under a light intensity of 100 mW cm\\u22122. The IPCEs of the PSCs were measured using a solar cell quantum efficiency measurement system (Newport, USA). Electrochemical impedance spectroscopy (EIS) measurements were performed on a CHI660E Electrochemical Workstation (Chen Hua, China) at a bias voltage of 0.7 V in the dark. The thickness and the optical parameters were measured using a dual rotating-compensator (ME-L ellipsometer, Wuhan Eoptics Technology Co., Wuhan, China). Each solar cell device had an active area of 0.11 cm2 and was measured in air.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Rhodamine 101 | LiF,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 95,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 125,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The solar cell structure was FTO/bl-TiO2/mp-TiO2/CH3NH3PbI3\\u2212xClx/Spiro-MeOTAD/Au. The FTO (sheet resistance 10 \\u03a9 square\\u22121) substrate was cleaned with soap, deionized water, acetone and ethanol sequentially. The methods of preparing compact TiO2 (bl-TiO2) and mesoporous TiO2 (mp-TiO2) layers had been described in detail in our previous report. The perovskite films were prepared by one-step spin coating procedure via the hybrid solution. Typically, the CH3NH3I (prepared by the reported procedure ) was mixed with PbCl2 (Alfar Aesar) and PbI2 (Alfar Aesar). The mole ratio of PbCl2:PbI2:CH3NH3I was controlled to be 1:1:4 in DMF (Alfar Aesar). The hybrid solution was kept being stirred at room temperature for 2 h to obtain perovskite precursor solution with varied concentration of 40 wt%, 45 wt% and 50 wt%, respectively. And lastly, the precursor solution was filtered with a PTFE filter (0.45 \\u03bcm pore size) to obtain more transparent perovskite precursor solution.\\nTo deposit perovskite film, TiO2 substrates and precursor solution were transferred to the glove box with water content less than 50 ppm. Then the TiO2 substrates and precursor solution were heated at 70 \\u00b0C for 1 h. The perovskite precursor solution was spin-coated on the mp-TiO2 substrate with spinning speed of 4000 rpm for 60 s. The coated perovskite films were then placed in drying cabinet at room temperature for 1 h (under relative humidity of 20%), followed by thermal annealing on the hot plate at 100 \\u00b0C for 75 min under relative humidity below 5%. The color of perovskite film was brown black in the end of preparation.\\nFor depositing hole transport layer, Spiro-MeOTAD (Luminescence Corp) was mixed in chlorobenzene solution (73 mg/1 mL), including 20 \\u03bcL of tert-butylpyridine (t-BP) and 17.5 \\u03bcL of Li-bis(trifluoromethanesulfonyl)-imide (Li-TFSI) dissolved in acetonitrile (520 mg mL\\u22121). The Spiro-MeOTAD was spin-coated on perovskite film at 2000 rpm for 30 s. And then a layer of 100 nm Au was deposited on the top of the devices by thermal evaporation.\\n\\nTransmittance spectra of perovskite films were recorded by a Perkin Elmer Lambda 950 UV-Vis Spectrometer. XRD was performed by DX-2600 X-ray diffractometer (Dandong Fangyuan Instrument Company) with Cu-K\\u03b1 radiation (scan range from 10\\u00b0 to 70\\u00b0). Film morphology was observed by field emission scanning electron microscope (Hitachi S-4300). Time-resolved photoluminescence of perovskite films was characterized by an Edinburgh Instruments FLS 980 fluorescence spectrometer. The I\\u2013V characteristic was measured with Keithley 2400 SourceMeter under simulated AM1.5 G (Sun 2000 solar simulator, ABET technologies) with irradiation power density of 100 mW cm\\u22122 and calibrated with a GaAs reference cell. Device area was typically 0.07 cm2 and the area of the devices for EQE measurements (QEX10, PV Measurements, Inc.) was 0.18 cm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 75,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"NVF (N-vinylformamide, 98%), azoisobutyronitrile (AIBN, 98%), potassium-tert-butoxide (95%), bis(2-bromoethyl)ether (BBE, 95%), dicyclohexyl-18-crown-6 (98%), anhydrous tetrahydrofuran (THF, 99.9%), and ethanol (99.9%), poly(1-vinylpyrrolidone-co-vinyl acetate) (PVP-co-PVA, Mn \\u223c 50000 g mol\\u22121), anhydrous sodium sulphate (100%), chloroform (99.9%), NaCl (100%), toluene (99.8%), chlorobenzene (CBZ, 99.8%), isopropanol (IPA, anhydrous, 99.5%), 4-tert-butylpyridine (TBP, 96%) and lithium bistrifluoromethanesulfonimidate (LiTFSI, 99.95%) were all purchased from Aldrich and used as received. Methylamine solution (33 wt% in absolute ethanol) and HI (57 wt%), titanium diisopropoxide bis(acetylacetonate) (TDB) (75 wt% in IPA), PbCl2 (98%) and DMSO (99.7%) were also purchased from Aldrich and used as received. MAI was synthesised and purified using the method previously reported. Titania paste (TiO2, 18 NRT) was purchased from Dyesol and used as received. Spiro-MeOTAD (Spiro, N2,N2,N2\\u2032,N2\\u2032,N7,N7,N7\\u2032,N7\\u2032-octakis(4-methoxyphenyl)-9,9\\u2032-spirobi[9H-fluorene]-2,2\\u2032,7,7\\u2032-tetramine, Fenglin Chemicals, 99.5%) was also used as received. Water was of ultrahigh purity and de-ionised. NVEE was synthesised and characterised using the methods described previously.\\n\\nPNVF\\u2013NVEE MGs were prepared by non-aqueous dispersion polymerisation following a method described previously. Briefly, a mixture of NVF (6.00 g, 85.5 mmol), PVP-co-PVA (1.80 g) and NVEE (1.79 g, 8.28 mmol) were added to ethanol (EtOH, 86 mL) in a round bottomed flask equipped with overhead stirrer, nitrogen supply and a reflux condenser. The solution was heated to 70 \\u00b0C and stirred vigorously. Then, AIBN (0.240 g, 1.45 mmol) in EtOH (2.0 mL) was added and the polymerisation allowed to continue for 1 h. The dispersion was filtered after cooling to 0 \\u00b0C with a 50 \\u03bcm mesh filter and then purified by repeated centrifugation and re-dispersion in EtOH. To transfer the MGs from EtOH to DMSO, the MGs in EtOH were centrifuged and then redispersed in DMSO. The particles were centrifuged once more and re-dispersed in DMSO.\\n\\nITO-coated glass substrates (20 \\u03a9 sq\\u22121) were cleaned by ultrasonication in a 1.0 wt% Hellmanex solution, rinsed with water, followed by IPA, NaOH (2.5 M) and then rinsed with water and dried. A TiO2 hole blocking layer (bl-TiO2) (60 nm) was spin-coated at 2000 rpm for 60 s onto the ITO using TDP solution in 1-butanol (0.15 M) and subsequent heating at 125 \\u00b0C for 5 min. The process was repeated using a 0.30 M TDP solution. After that, TiO2 paste (1:5 in EtOH) was spin coated at 5000 rpm for 30 s onto the cleaned ITO substrate to form a mesoporous scaffold (meso-TiO2). The meso-TiO2 film (thickness \\u223c250 nm) was annealed at 500 \\u00b0C for 30 min and cooled to room temperature. Then a MAPbI3\\u2212zClz precursor solution in DMSO (100 \\u03bcL) containing MGs was spin-coated onto ITO/bl-TiO2/meso-TiO2 substrate at 4000 rpm for 25 s. The MAPbI3\\u2212zClz/MG films are denoted as MPxMGy where x and y are, respectively, the concentrations of MAPbI3\\u2212zClz (assuming 100% conversion) and MG in the mixed solution used for spin coating. The MAPbI3\\u2212zClz solution contained the precursors MAI and PbCl2 at a 3:1 molar ratio. During the spin coating process, toluene (500 \\u03bcL) was dripped onto the surface at a uniform rate over the last 15 s. The nominal compositions of the MPxMGy films studied are shown in Fig. 2. The films were dried at 100 \\u00b0C for 45 min and then stored in a desiccator over P2O5 in the dark until investigation.\\n\\nDynamic light scattering (DLS) measurements were conducted using a Malvern Zetasizer Nano ZS instrument (via cumulants analysis) and provided the z-average diameter (dz) and polydispersity index (PDI) for the dispersed MGs. The top view SEM images were obtained using a Philips XL30 FEGSEM. The cross-section SEM images and EDX spectra were obtained using a Carl Zeiss Sigma FE-SEM and an AG-ULTRA 55. The samples were coated with Au or Pd. AFM images were obtained using either a Bruker Multimode 8 or a Bruker Catalyst. AFM images were captured in ScanAsyst\\u2122 (Peak Force Tapping) mode. UV-visible spectra were recorded using a Perkin Elmer Lamda 25 UV-Vis spectrometer. Film thickness measurements were conducted using a Dektak 8 Stylus Profilometer (Bruker). XRD patterns were conducted using a Bruker D8 Advance diffractometer (Cu-K\\u03b1). Films were scanned with a step size of 0.02\\u00b0. The films were prepared under a nitrogen atmosphere and measured using an airtight holder. Photoluminescence (PL) spectra were obtained using an Edinburgh Instruments FLS980 spectrometer. The beam was incident on the film surface side and an excitation wavelength of 480 nm was used.\\n\\nDemonstration solar cells were prepared using MP37.5MG3.0 and compared with control MP37.5 devices. The procedure to prepare the ITO/bl-TiO2/meso-TiO2/MPxMGy films was described above. CBZ was used as the HTM solvent at room temperature. LiTFSI (4.8 \\u03bcL, 520 mg mL\\u22121) and TBP (8.0 \\u03bcL) were also added to the Spiro solution following our method reported earlier. The Spiro HTM films (200 nm) were formed by spin coating at 4000 rpm for 20 s onto the MPxMGy films. The devices were coated with a gold layer (70 nm) using thermal evaporation. The geometry of these PSCs is depicted in Fig. 9. The ITO/bl-TiO2/meso-TiO2/MP37.5/Spiro/Au devices did not contain added MGs and were the control. Although both types of devices were not optimised for efficiency, they were prepared using identical conditions and are, therefore, directly comparable.\\nThe current density\\u2013voltage (J\\u2013V) characteristics were measured using a Keithley 2420 Sourcemeter and 100 mW cm2 illumination (AM 1.5G) and a calibrated NREL certified Oriel Si-reference cell. An Oriel solar simulator (SOL3A) was used for these measurements. The active area of the devices (0.025 cm2) was determined using a square aperture within a mask. The data shown are from the reverse scan (Voc to Jsc) and the sweep rate was 100 mV s\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl; PNVF\\u2013NVE,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.025,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The CH3NH3PbI3\\u2212xClx perovskite was synthesized as already reported. Firstly, CH3NH3I was synthesized by reacting 27.86 mL methylamine (40 wt% in methanol, Junsei Chemical Co.) and 30 mL hydroiodic acid (57 wt% in water, Aldrich) in a round-bottomed flask at 0 \\u00b0C for 2 hours with stirring. The resulting materials were obtained in the process of evaporation and recrystallization and dried at 60 \\u00b0C in a vacuum oven overnight. Then, synthesized CH3NH3I powder was mixed with PbCl2 (Aldrich) with a ratio of 40 wt% in dimethylformamide (DMF).\\n\\nSolar cell devices were fabricated on 40 \\u00d7 40 mm fluorine-doped tin oxide (FTO) coated glass substrates. The FTO coated glass substrates were etched by brushing with zinc powder and 2 M hydrochloric acid (HCl). Then, they were washed using detergent, deionized water (DI-water), acetone and isopropyl alcohol (IPA). The FTO coated glass substrates were under UV-ozone treatment for 15 minutes, and then coated by TiO2 compact layer at 2000 rpm for 60 seconds as reported. The coated films were sintered at 500 \\u00b0C. Al2O3 (1:2 vol%, Aldrich) layer was coated on them at 2500 rpm for 60 seconds and annealed at 150 \\u00b0C for 1 hour. The perovskite solution was spin-coated at 2000 rpm for 30 seconds, and then slowly annealed at 100 \\u00b0C for 2 hours. Spiro-MeOTAD solution (83.3292 mg mL\\u22121 in CB) with addition of Li-TFSI in acetonitrile (0.18 M) and tert-butylpyridine (1 mL in 9 mL CB) were spin-coated on the films at different speed, and oxidized for 24 hours. Finally, silver electrodes (120 nm) were vacuum-deposited at the pressure of \\u223c10\\u22127 torr. Devices for space-charge-limited-current (SCLC) measurement were fabricated on the 25 \\u00d7 25 mm indium tin oxide (ITO) coated glass substrates. Firstly, they were washed using detergent, DI-water, acetone and IPA. After washing, the substrates were dried in the 150 \\u00b0C oven overnight and UV-ozone-treated for 15 minutes. PEDOT-PSS (Clevios P, VP AI 4083) was spin-coated on the substrates in the condition of 5000 rpm/30 seconds and annealed at 150 \\u00b0C for 10 minutes. The spiro-MeOTAD solution in above condition was spin-coated at different speed on the PEDOT-PSS layer. After then, gold electrodes (100 nm) were deposited in a vacuum condition.\\n\\nUsing a Keithley 2400 SMU and an Oriel xenon lamp (450 W) with an AM1.5 filter, the solar cells were characterized in air under AM 1.5G illumination of 100 mW cm\\u22122 (Oriel 1 kW solar simulator), which was calibrated with a KG5 filter certified by NREL. The J\\u2013V curves of all devices were measured with 0.09 cm2 of active area. SCLC was also measured in the same condition but in dark condition.\\n\\nThe atomic force microscope (using a VEECO Dimension 3100 + Nanoscope V) was operated in tapping mode to acquire the images of the surfaces of perovskite and HTL coated on the perovskite film.\\n\\nThe secondary ion mass spectroscopy (SIMS) (IMS 6F with Cs+ gun, CAMECA) was operated to acquire the atomic depth profile of perovskite hybrid solar cells.\\n\\nPhoto-CELIV was conducted on FTO/bl-TiO2/Al2O3/CH3NH3PbI3\\u2212xClx/spiro-MeOTAD/Ag devices in ambient air. The active area was defined by the size of the counter-electrode (0.09 cm2).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | Al2O3-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 120,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned ITO glass substrates (12\\u202fmm\\u202f\\u00d7\\u202f12\\u202fmm) have a sheet resistance of 15\\u202f\\u03a9/\\u25a1. The substrates were sequentially washed with Hellmanex III, deionized water, acetone and isopropanol in 10\\u202fmin cycle. The substrates were treated in UV-ozone cleaner for 20\\u202fmin prior to use. For electron transport layer, SnO2 has been deposited on ITO substrate using method from Ref.\\u00a0[]. The mix-cation perovskite absorbers (FA0.4MA0.6PbI2.8Br0.2) were prepared by one-step method with gas quenching. 414.9\\u202fmg lead (II) iodide (PbI2), 68.8\\u202fmg formamidinium iodide (FAI) and 95.4\\u202fmg methylammonium iodide (MAI) and 36.7\\u202fmg lead (II) bromide (PbBr2) were dissolved 1\\u202fml\\u202fN,N-Dimethylformamide (DMF) and stirred for 12\\u202fh at 60\\u202f\\u00b0C. The solution was spin coated on substrate at a spin rate of 4000\\u202frpm for 30\\u202fs. During the spin coating, nitrogen gas was applied on the substrates for 10\\u202fs. The as-deposit substrates were quickly transferred to a hotplate and dried at 60\\u202f\\u00b0C for 1\\u202fmin. At last, the dry samples were annealed for 10\\u202fmin, resulted in 350\\u202fnm thick film. For the HTL, Avantama P-10 tungsten oxide nanoparticle precursor had been added to water-free PEDOT:PSS (Clevios P SB 5) in different ratios. The HTL precursor solution was spin-coated at a spin-rate of 5000\\u202frpm for 30\\u202fs in glove box. To complete the device, 2\\u202fnm MoO3 layer and 100\\u202fnm Ag layer were evaporated on top of hole transport layer sequentially (evaporation rate: 0.2\\u202f\\u00c5/s for MoO3 and 2\\u202f\\u00c5/s for Ag, vacuum level: 1\\u202f\\u00d7\\u202f10\\u22126\\u202fmbar). The overall device structure is ITO/SnO2/FA0.4MA0.6PbI2.8Br0.2/ PEDOT:PSS/MoO3/Ag, as shown in Fig.\\u00a01 and the active device area is 4.5\\u202fmm2.\\n\\nThe current density \\u2013 voltage (J-V) measurements were conducted on a I\\u2013V testing system equipped with Keithley 2400 source meter from PV Measurements, Inc. under 1 sun intensity (100\\u202fmW/cm2) with AM 1.5G filter. External quantum efficiency (EQE) measurement has been carried on PV Measurements QEX7 Spectral Response System. The surface topology images were captured by NanoSEM 450 (scanning electron microscopy) fitted with a retractable annular backscattered electron detector as well as a Bruker SDD-EDS detector. The surface roughness was detected by Bruker Dimension ICON SPM (atomic force microscopy) on contact mode with scan size: 5\\u202f\\u03bcm\\u202f\\u00d7\\u202f5\\u202f\\u03bcm and samples/line: 512. The conductive AFM measurement was conducted on JEOL JSPM 5400 MkII under 0.5\\u202fV bias voltage. The impedance analysis was performed on Autolab PGSTAT-30 analyzer inside N2 filled glovebox. The frequency analyzer module is in the frequency range of 106\\u2013100\\u202fHz and AC oscillating amplitude was as low as 20\\u202fmV (rms) to maintain the linearity of the response.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.4MA0.6PbBr0.2I2.8,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60,\\n Perovskite_deposition_thermal_annealing_time: 1,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 504,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 45,\\n Cell_area_measured: 0.045,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Following the literature procedure, a mixture of hexaketocyclohexane octahydrate\\u00a0(4.45\\u00a0mmol) and 4-((3-bromopropyl)thio)-5-fluorobenzene-1,2-diamine (13.36\\u00a0mmol) was added to deoxygenated acetic acid (125\\u00a0mL). The mixture was refluxed for 16\\u00a0hr. After the mixture was cooled to room temperature, it was poured into ice water (400\\u00a0mL) and the resulting precipitate was filtered and washed by using dichloromethane. The organic phase was dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified by silica-gel column chromatography with DCM/EtOAc (5:1) as eluent to give S1 as a yellowish-brown solid (43%). 1H NMR (300 MHz, CDCl3): \\u03b4 8.51\\u20137.56 (m, 6H), 3.67 (s, 6H), 3.36 (s, 6H), 2.43 (s, 6H); 13C NMR (75 MHz, CDCl3): \\u03b4 162.85, 159.44, 142.34, 140.77, 136.50, 136.22, 125.67, 112.71, 112.42, 31.44, 31.08, 30.01.\\n\\nFollowing the literature procedure, to a solution of methylacrylic acid (216\\u00a0mg, 3.00\\u00a0mmol) in N,N-dimethylformamide (DMF) (5\\u00a0mL) in a 50-mL round-bottom flask equipped with a reflux condenser at 0\\u00b0C was added K2CO3 (415\\u00a0mg, 3.00\\u00a0mmol). After 45\\u00a0min, the S1 (2.50\\u00a0mmol) in DMF (3\\u00a0mL) was added dropwise, and the reaction mixture was stirred at 90\\u00b0C for 24\\u00a0hr under Ar. The reaction mixture was cooled to room temperature, quenched with water (20\\u00a0mL), and extracted with DCM. The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by silica-gel column chromatography using hexane-EtOAc as the eluent to give the corresponding product S2. 1H NMR (300 MHz, CDCl3):\\u03b4 8.27 (dq, J\\u00a0= 4.4, 2.2\\u00a0Hz, 3H), 8.15 (ddd, J\\u00a0= 9.2, 6.4, 2.3\\u00a0Hz, 3H), 6.20 (d, J\\u00a0= 4.6\\u00a0Hz, 3H), 5.85\\u20135.47 (m, 3H), 4.41 (t, J\\u00a0= 6.0\\u00a0Hz, 6H), 3.32 (t, J\\u00a0= 7.0\\u00a0Hz, 6H), 2.30 (p, J\\u00a0= 6.5\\u00a0Hz, 6H), 2.00 (d, J\\u00a0= 3.8\\u00a0Hz, 9H); 13C NMR (125 MHz, CDCl3):\\u00a0\\u03b4 167.37, 162.24, 160.19, 142.79, 142.52, 142.37, 142.23, 141.04, 137.21, 136.95, 136.14, 126.21, 125.13, 112.63, 63.04, 28.11, 27.39, 18.56.\\n\\nFollowing the literature procedure, a solution of m-chloroperbenzoic acid (m-CPBA, 0.90\\u00a0mmol) in CH2Cl2 (15\\u00a0mL) was added dropwise to a stirred solution of S2 (0.30\\u00a0mmol) in CH2Cl2 (20\\u00a0mL) at 0\\u00b0C and the stirring was continued for 3\\u00a0hr at 0\\u00b0C. The reaction mixture was washed with water, saturated NaHCO3 solution, and water successively. The organic layer was dried and concentrated following by column chromatography on silica-gel column with DCM/acetone (v/v\\u00a0= 8/1) as eluent to afford S3. Rf (CH2Cl2/acetone 10:1): 0.25; ESI-MS (HR): calculated [C45H40F3N6O9S3]+: 961.6915, found: 961.1973. 1H NMR (300 MHz, CDCl3): \\u03b4 9.21 (dt, J\\u00a0= 6.2, 3.0\\u00a0Hz, 3H), 8.37 (dt, J\\u00a0= 9.7, 2.8\\u00a0Hz, 3H), 6.09 (s, 3H), 5.73\\u20135.39 (m,\\u00a03H), 4.49\\u20134.06 (m, 6H), 3.40 (td, J\\u00a0= 13.7, 6.8\\u00a0Hz, 3H), 3.27\\u20133.00 (m, 3H), 2.43 (dq, J\\u00a0= 14.8, 8.9, 7.4\\u00a0Hz, 3H), 2.13\\u20131.98 (m, 3H), 1.92 (s, 9H); 13C NMR (75 MHz, CDCl3): \\u03b4 167.14, 160.92, 157.53, 145.80, 145.71, 145.59, 145.54, 145.41, 144.70, 144.54, 144.40, 144.23, 143.73, 143.56, 143.40, 143.23, 141.04, 136.14, 130.92, 130.88, 125.99, 114.81, 114.52, 62.85, 51.15, 21.53, 18.31.\\n\\n\\nAll chemicals and reagents were purchased from Sigma-Aldrich and used as received without further purification. All solutions are filtered with a 0.45-\\u03bcm PTFE filter before use. CH3NH3I was synthesized according to the reported procedure. For the typical synthesis, 0.3\\u00a0mol (38\\u00a0mL) methylamine (CH3NH2) solution (33 wt.% in absolute ethanol) was reacted with equimolar (40\\u00a0mL) hydroiodic acid (HI) (57\\u00a0wt.% in water) with stirring in ice bath for 2\\u00a0hr to obtain methylammonium iodide (CH3NH3I). Crystallization of CH3NH3I was achieved using a rotary evaporator at 60\\u00b0C for 2\\u20133\\u00a0hr.\\nAll the ITO-coated substrates were cleaned with isopropanol, acetone, and distilled water sequentially, and treated with UV-ozone for 20\\u00a0min. To prepare NiO HTL, Nickel(II) acetylacetonate was dissolved in ethanol (0.1 mol/L) with the addition of 10\\u00a0\\u03bcL of HCl (38 wt.%) into the solution. The solution was then stirred in a sealed glass vial overnight. ITO-coated glass substrates were cleaned and then UV-ozone treated for 15\\u00a0min prior to depositing the NiO layer. The NiO layer was then spin-coated onto the ITO-coated glass at 5,000\\u00a0rpm for 30\\u00a0s and annealed at 350\\u00b0C for 1\\u00a0hr in air. To prepare crosslinked HTL, a precursor solution of TCTA-BVP mixed with pentaerythritol tetrakis(3-mercaptopropionate) (PETMP) with a molar ratio of 2.2:1 in chlorobenzene (8\\u00a0mg/mL of TCTA-BVP) was prepared first. Then the precursor solution (1\\u00a0mL) was doped by adding 10\\u00a0\\u03bcL of t-butylpyridine (TBP) solution and 10\\u00a0\\u03bcL of Li-bis(trifluoromethanesulfonyl)imide (Li-TFSI)/acetonitrile (170\\u00a0mg/mL) additives. After shaking for 1\\u00a0min, the doped precursor solution was spin-coated on top of perovskite layer at 2,000\\u00a0rpm for 30\\u00a0s and 4,000\\u00a0rpm for 5 s. The resulting films were heated on a hotplate in the nitrogen glovebox at a temperature 150\\u00b0C for 30\\u00a0min. After cooling, the film was rinsed with toluene on the surface and then spun at 2,000\\u00a0rpm for 30 s.\\nFor preparation of the perovskite layer, the precursor solution was prepared by mixing CH3NH3I with lead(II) iodide (PbI2) at a molar ratio of 1:1.08 in the DMF and DMSO co-solvent (with a volume ratio of 4:1) and stirred at 60\\u00b0C overnight. The perovskite precursor solution was then spin-coated onto prepared HTL at 1,000\\u00a0rpm for 15\\u00a0s and 4,000\\u00a0rpm for 45 s. During the last 25\\u00a0s of the second spin-coating step, the substrate was treated with toluene drop-rinsing (0.7\\u00a0mL). The as-spun films were annealed at 100\\u00b0C for \\u223c20\\u00a0min.\\nFor preparation of the ETL, the HATNASOACRYLATE precursor solution was first mixed with PETMP at a molar ratio of 5:1 in chlorobenzene (15\\u00a0mg/mL in 1,4-dichlorobenzene). The precursor solution (1\\u00a0mL) was then doped by adding triethylamine with different concentration (1 wt.%, 3 wt.%, and 5 wt.%, triethylamine to HATNASOACRYLATE). The solution was deposited onto perovskite layer by spin-coating at 2,000\\u00a0rpm for 30\\u00a0s and 4,000\\u00a0rpm for 5 s. The controlled PCBM layer (20\\u00a0mg/mL in 1,4-dichlorobenzene) was also spin-coated at 2,000\\u00a0rpm for 30\\u00a0s and 4,000\\u00a0rpm for 5 s. All of the ETL layer was coated with a bis-C60 surfactant layer. The bis-C60 layer was prepared (2\\u00a0mg mL\\u22121) in isopropyl alcohol and spin-coated at 3,000\\u00a0rpm for 30 s. The all-crosslinked CTLs flexible PVSCs used an ITO-coated PEN substrate, which were cleaned with isopropanol, acetone, and distilled water sequentially, and treated with UV-ozone for 20\\u00a0min. The crosslinked HTL (c-TCTA-BVP), MAPbI3 perovskite layer, and crosslinked ETL (c-HATNA) were deposited sequentially using the same procedure described above. Finally, for all devices above, a 150-nm-thick top Ag electrode was evaporated under high vacuum (<2\\u00a0\\u00d7 10\\u22127 torr) through a shadow mask with 1.4-mm wide patterned ITO bar and the 8\\u00a0mm length. For all studied devices, the device area was defined as 9.6\\u00a0mm2 by metal shadow mask.\\nAll the J-V curves in this study were recorded by using a Keithley 2400 source measurement unit and the scan rate was kept at 0.1\\u00a0V s\\u22121. The J-V curves and steady-state power output of the PVSCs were measured by a Keithley 2400 Source Meter under illumination by a 450-W Oriel xenon lamp with an AM 1.5G filter solar simulator (100 mW cm\\u22122), and the light intensity was calibrated with a standard Si photodiode detector (equipped with a KG-5 filter), which can be traced back to the standard cell of National Renewable Energy Laboratory. The EQE spectra were measured using a setup consisting of a xenon lamp (Oriel, 300 W) as a light source, a monochromator (Newport Cornerstone 130), a chopper with a frequency of 100\\u00a0Hz, a lock-in amplifier (Stanford Research Corp SR830), an SMU (Keithley 2400), and a NIST-certified Si photodiode (Thorlabs FDS 100-CAL) for calibration. White light bias was applied using a 50-W LED fiber-optic illuminator; no change was observed in the EQE measurements with and without white light bias. The EQE spectrum was integrated over AM 1.5G photon flux to attain photocurrent density. The fluctuation of xenon arc lamp source was within 5% during the entire period of measurement. Charge-carrier mobilities (\\u03bc) were calculated from the J-V characteristics using the SCLC method with the Mott-Gurney equation for the current density J SCLC expressed as J=9\\u025br\\u025b0\\u03bcV28L3, where \\u025b 0 is the vacuum permittivity, \\u025b r is the dielectric constant of the film, and L is the thickness of the active layer. The morphology of the perovskite films were characterized by scanning EM (FEI Sirion XL30 scanning electron microscope operated at 5 kV). The absorption spectra were measured by a Varian Cary 5000\\u00a0UV-Vis-NIR. Fourier transform infrared spectra were collected by a Bruker Vector 33 Fourier transform infrared spectrophotometer. All stability testing results were measured from 20 devices under each condition.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: c-HATNA | bis-C60,\\n ETL_additives_compounds: Triethylamine | Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 70.0; 70.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 100,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lawesson\\u2019s reagent, diphenylamine, and all other chemical reagents, unless otherwise specified, were used as received. Compound 1 (Rodr\\u00edguez et al., 2006), compound 2 (Rakstys et al., 2016), were synthesized according to the literatures. 4-methoxydiphenylamine (3), and 4,4\\u0301-dimethoxydiphenylamine (4) were synthesized through Buchwald\\u2013Hartwig coupling (Scheme 1 ) from relative starting material 4-bromoanisole, aniline, and 4-methoxyaniline. Solvents were distilled over appropriate drying agents and used or stored under a N2 atmosphere.\\n\\nHTM-2: A mixture of 2 (462\\u202fmg, 0.718\\u202fmmol, 1 equiv), 3 (715\\u202fmg, 3.59\\u202fmmol, 5 equiv), NaOtBu (414\\u202fmg, 4.31\\u202fmmol, 6 equiv), Pd2(dba)3 (0.15 equiv), and PtBu3 (0.3 equiv) in dry toluene (20\\u202fmL) was heated under reflux overnight in a 100-mL flask under N2. After cooling, the toluene was removed and the residual mixture was with CH2Cl2/H2O; the combined organic phases were dried (MgSO4) and concentrated. The residue was purified chromatographically (SiO2; EtOAc/hexane, 1:4). Yield: 65.6%. 1H NMR (400\\u202fMHz, CDCl3): \\u03b4 8.03 (4H), 7.34 (d, J\\u202f=\\u202f8\\u202fHz, 4H), 7.15 (8H), 6.91\\u20136.75 (24H), 6.74 (8H), 3.76 (12H). HRMS (FAB, m/z): [M\\u202f+\\u202fH+] calcd for C78H60N4O4, 996.4192; found 996.4182.\\nHTM-1 (Park et al., 2014) and HTM-3 (Rakstys et al., 2016) were synthesized using the general procedure described above. HTM-1: 1H NMR (400\\u202fMHz, CDCl3): \\u03b4 8.03 (4H), 7.36 (4H), 7.16\\u20137.12 (16H), 6.93\\u20136.88 (28H). HRMS (FAB, m/z): [M\\u202f+\\u202fH+] calcd for C74H52N4, 1116.46091; found 1116.46083. HTM-3: 1H NMR (400\\u202fMHz, CDCl3): \\u03b4 7.99 (4H), 7.27 (4H), 6.86\\u20136.85 (20H), 6.75\\u20136.73 (16H), 3.76 (24H). HRMS (FAB, m/z): [M\\u202f+\\u202fH] calcd for C82H69N4O8, 1237.51099; found 1237.51076.\\n\\nThe perovskite solution (CH3NH3PbI3) was prepared according to a procedure described previously (Chiang et al., 2017). That is, the MAPbI3 precursor solution was prepared by dissolving 1.15\\u202fM PbI2 and MAI (methyl ammonium iodide) (molar ratio, 1:1) into anhydrous DMF/DMSO (4:1). The solution was stirred at 60\\u202f\\u00b0C for 2\\u202fh in a glove box to form the perovskite solution. The perovskite precursor solutions were then spin-coated on the HTL-coated substrates. The corresponding fabricated inverted PSC devices has the configuration indium tin oxide (ITO)/HTL/perovskite/PC61BM/BCP/Ag. The ITO glass substrate was patterned through an etching process, follow by cleaning and treatment with plasmas for 5\\u202fmin. The HTL material (PEDOT:PSS or HTM-1\\u20133) was deposited on the ITO through spin-coating (4000\\u202frpm, 30\\u202fs) and annealing (120\\u202f\\u00b0C, 20\\u202fmin) for PEDOT:PSS and through spin-coating (2000\\u202frpm, 20\\u202fs) for the HTM series; the film thickness of PEDOT:PSS and the HTM series were 40 and 10\\u202fnm, respectively. A perovskite solution was spin-coated at 2000\\u202frpm for 10\\u202fs and then at 4000\\u202frpm for 10\\u202fs, and then washed with toluene; the thickness of the resulting film of perovskite was approximately 500\\u202fnm. Solutions of PC61BM was spin-coated at 2000\\u202frpm for 20\\u202fs and BCP was then spin-coated at 6000\\u202frpm for 10\\u202fs; the thicknesses of the resulting PC61BM and BCP films were 35 and 2\\u202fnm, respectively. Finally, the device was completed by depositing a 100-nm-thick layer of Ag through thermal evaporation (<10\\u22126\\u202ftorr). The active area of the device was 0.1\\u202fcm2. In this work, all devices were fabricated under the optimized film thickness. For example, the PEDOT:PSS with 40\\u202fnm film thickness was prepared according to the pervious literature (Hsu et al., 2015). In addition, the film thickness of the bifluorenylidene-based HTMs (HTM-1\\u20133) were firstly referring to the literature that used HTM-3 as hole transporting material in n-i-p PSC (Rakstys et al., 2016). Then, optimized the cell performance as the film thickness at around 10\\u202fnm.\\n\\nThe hole transport mobilities of the HTMs were determined through space charge limited current (SCLC) measurements. Hole-only devices were prepared having the configuration ITO/HTM/MoO3/Ag. The ITO glass substrate was patterned through etching, followed by cleaning and treatment with plasmas for 5\\u202fmin. A solution of the HTM was then spin-coated (2000\\u202frpm, 20\\u202fs) onto the ITO. MoO3 and the Ag electrode were thermally evaporated to give films having thicknesses of 3 and 100\\u202fnm, respectively. The Mott\\u2013Gurney equation was used to calculate the hole-only mobilities in the SCLC regime (Eq. (1)) (Goh et al., 2005). J=98\\u03b5\\u03b50\\u03bchV2L3\\n\\n1H NMR spectra were recorded using a Bruker 400-MHz spectrometer. High-resolution mass spectra (HRMS, FAB) were recorded using a Bruker solariX mass spectrometer. Ultraviolet\\u2013visible (UV\\u2013Vis) spectra were recorded using a Dyanmica DB-20 UV\\u2013Vis spectrophotometer. Photoluminescence (PL) spectra were recorded using an F-4500 fluorescence spectrophotometer. Cyclic voltammetry (CV) was conducted using a BioLogic SP-150 apparatus operated at a scan rate of 100\\u202fmV\\u202fs\\u22121. All measurements were carried out at room temperature with a conventional three electrode configuration consisting of a platinum working electrode, an auxiliary electrodes and a non-aqueous Ag/AgNO3 reference electrode. Glass transition temperatures (T g) were recorded using by TA Instruments DSC 2920 apparatus operated at a heating rate of 10\\u202f\\u00b0C\\u202fmin\\u22121 from 30 to 300\\u202f\\u00b0C under a N2 atmosphere. Thermogravimetric analysis (TGA) was performed using a TA Instruments SDT 2960 Simultaneous DTA-TGA; samples (3\\u20135\\u202fmg) were subjected to heating at a rate of 15\\u202f\\u00b0C\\u202fmin\\u22121 under a flow of N2. Surface images were recorded through field-emission scanning electron microscopy (FE-SEM) using a JEOL JSM 6701G microscope. The morphologies of the films were analyzed through atomic force microscopy (AFM), using a Bruker Dimension Edge microscope operated in the dynamic force mode at ambient temperature; the Si photomultiplier sensor exhibited a resonance frequency of 160\\u202fkHz and a force constant of 7.4\\u202fN\\u202fm\\u22121. Contact angles of the films were measured using a First ten angstroms/FTA-1000B apparatus. The cell performance was measured inside a glove box. The current\\u2013voltage (I\\u2013V) properties of the PSCs were measured using a computer-controlled Keithley 2400 source measurement unit and a Peccell solar simulator under AM 1.5G illumination (1000\\u202fW\\u202fm\\u22122). The illumination intensity was calibrated using a standard Si reference cell and KG-5 filter.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: HTM-2,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Ambient,\\n Stability_time_total_exposure: 700,\\n Stability_PCE_initial_value: 12,\\n Stability_PCE_end_of_experiment: 73,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO glasses (1.5 cm \\u00d7 1.5 cm) were bought from OPVtech (China). Magnesium nitrate (Mg(NO3)2) was purchased from Beijing Tong Guang Fine Chemicals (China) Co., Ltd. Butvar\\u00ae B-76 Polyvinyl butyral was obtained from Aladdin (China). Ethanolamine (EA) was bought from Xilong Scientific (China). Chloroform (CHCl3) was obtained from Tianjin Jingdongtianzheng Precision Chemical Reagent Factory (China). SnO2 nanoparticles (15% in water colloidal dispersion), PbBr2 and PbI2 were purchased from Alfa Aesar. CH3NH3I (MAI), CH3NH3Br (MABr), HC(NH2)2I (FAI) and Spiro-OMeTAD were obtained from Xi'an Polymer Light Technology (China) Co., Ltd. Chlorobenzene (CB), N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), ethanol, propanoic acid, 4-tert-butylpyridine and lithium bis (trifluoromethylsulphonyl) imide were purchased from J & K (China) Co., Ltd. Cobalt(III) FK209 TFSI salt was bought from Dyesol (Australia) Co., Ltd. All reagents were used without further purification.\\n\\nFTO glasses were cleaned using ultrasonication in deionized water, acetone, and isopropanol, and then were dried in an oven at 65 \\u00b0C and treated with oxygen plasma for 3 min before spin-coating. In order to prepare the ETL, a mixture of ethanol and propionic acid (9:1, v/v) was used to prepare a solution of Mg(NO3)2 at a concentration of 0.045 M. Butvar\\u00ae B-76 Polyvinyl butyral of the same quality as Mg(NO3)2 was added to the above solution. The above Mg(NO3)2 solution was spin-coated on the FTO at 4000 rpm for 30 s, and then heated in a muffle furnace at 450 \\u00b0C for 1 h at a heating rate of 5 \\u00b0C min\\u22121 to prepare MgO modified FTO. The SnO2 colloidal solution was diluted 5 times with deionized water and spin coated onto FTO and MgO modified FTO at 4000 rpm for 30 s and then annealed in ambient air at 150 \\u00b0C for 30 min. Then, 30 \\u03bcL of EA was dissolved in 50 mL of CHCl3 to prepare an EA solution. The prepared SnO2 and MgO/SnO2 substrates were then immersed in the CHCl3 solution of EA for 5 h at 20 \\u00b0C and dried in a nitrogen flow, and then annealed in ambient air at 100 \\u00b0C for 30 min. For the perovskite film (Cs0.05FA0.81MA0.14PbI2.55Br0.45) preparation, a mixture of PbBr2 (0.2 M), PbI2 (1.1 M), MABr (0.2 M), and FAI (1 M) was dissolved in DMF:DMSO (4:1, v/v) and stirred for 12 h. Then, CsI was dissolved in DMSO and added to the above solution, followed by stirring at 60 \\u00b0C for 1 h to obtain the desired triple cation composition. The perovskite film was formed in situ on the ETL layer by spin-coating the precursor solution by using a consecutive two-step process at 1500 rpm and 6000 rpm for 15 s and 30 s, respectively. CB was dripped in the last 10 seconds. Then, the perovskite film was obtained after annealing at 110 \\u00b0C for 1 h. In order to prepare the hole transport layer (HTL), 70.1 mg of spiro-OMeTAD was dissolved in 1 mL of CB and stirred for 2 h to prepare the HTM precursor solution. Subsequently, 27.6 \\u03bcL of 4-tert-butylpyridine, 27.6 \\u03bcL of cobalt(III) FK209 in acetonitrile (300 mg mL\\u22121) and 16.8 \\u03bcL of Li-TFSI in acetonitrile (520 mg mL\\u22121) were added to the HTM precursor solution and stirred for 30 min. The HTL precursor solution was then deposited on the perovskite film by spin coating at 5000 rpm for 30 s. Finally, a 70 nm gold electrode was deposited on top of the cell by thermal evaporation.\\n\\nThe microstructure of the FTO, SnO2, MgO/SnO2/EA and perovskite films were observed by scanning electron microscopy (SEM) (Hitachi, SU8010). X-ray diffraction (XRD) was conducted using the PANalytical, Empyrean XRD (Cu K\\u03b1 1.5406 \\u00c5 radiation), and the surface chemical composition of the MgO, MgO/SnO2 and MgO/SnO2/EA films was obtained by X-ray photoelectron spectroscopy (XPS) (VG ESCALab 220i-XL photoelectron spectrometer with a monochromatic Al K\\u03b1 X-ray source). Ultraviolet photoelectron spectroscopy (UPS) was performed using a Thermo Scientific ESCALab 250Xi. A gas discharge lamp was used for UPS, with helium gas admitted and He I (21.22 eV) emission lines were employed. The helium pressure in the analysis chamber during analysis was about 10\\u22124 Pa, and the data were acquired with \\u221210 V bias. UV-Vis absorption spectra were recorded on a Hitachi UH4150. The current density\\u2013voltage (J\\u2013V) characteristics were obtained with a Keithley 2400 SourceMeter. Solar cells were recorded with the 10 mV s\\u22121 scan rate under ambient conditions without encapsulation. Light intensity was certified by using a standard Si solar cell. In all measurements, the solar cells were covered with a metal aperture mask to define the active area of 0.1 cm2. The external quantum efficiency (EQE) was measured using an Enlitech QE-R with a wavelength ranging from 300 to 800 nm. Photoluminescence (PL) was performed with a Hitachi F-4600 (excitation at 470 nm). Electrochemical impedance spectroscopy (EIS) was performed using a ZAHENR PP211 electrochemical workstation, the AC amplitude was set to 5 mV, and the scanning frequency was set between 1 and 106 Hz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: MgO | SnO2-np | Ethanol amine,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating | Dipp-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.81MA0.14PbBr0.45I2.55,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 110,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbI2 was purchased from TCI Chemicals; TiO2 paste (18NR-T) from Dyesol; Spiro-OMeTAD from Luminescence Technology Corp; 4-tert-butyl pyridine (TBP) and lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) from J&K Scientific Ltd; and zinc acetate, magnesium acetate and all solvents from Sinopharm Chemical Reagent. All chemicals were used as received. CH3NH3I was synthesized and purified as reported.\\n\\nPbI2 was dissolved in NMP and then tetrachloromethane was slowly diffused into the above solution for 24 h to generate yellow grain-like crystals.\\n\\nBefore the deposition of the ETL, fluorine-doped tin oxide (FTO) glass substrates were sequentially washed in ultrasonic baths of acetone, distilled water and ethanol. A compact ZnO-MgO-EA+ blocking layer as the ETL was prepared on clean FTO by our previously reported method: a solution of zinc acetate dihydrate (0.1 M), magnesium acetate tetrahydrate (0.1 M) and ethanolamine (0.01 M) in 2-methoxyethanol was spin-coated on the FTO substrate. The substrate was heated at 120 \\u00b0C for 15 min, and then annealed at 450 \\u00b0C for 30 min. After cooling to room temperature, the film was immersed in a 20 mM TiCl4 solution at 70 \\u00b0C for 30 min. After drying, a \\u223c200 nm thick mesoporous TiO2 film was deposited on the pre-treated FTO substrate by spin-coating of a TiO2 paste in ethanol (1:3, mass ratio), and annealing at 450 \\u00b0C for 30 min.\\nFor the MAPbI3 perovskite layer, 461 mg of PbI2 and 99 mg, 198 mg, 297 mg or 396 mg of NMP (molar ratio: 1:1, 1:2, 1:3 or 1:4) were dissolved in DMF with the same Pb2+ concentration (1.3 M) at room temperature for the preparation of the precursor solutions. Then the precursor solution was spin-coated on the prepared substrate at 4000 rpm for 25 s. Then a solution of CH3NH3I in 2-propanol (50 mg mL\\u22121) was added dropwise onto the film and spin-coated at 4000 rpm for 25 s. Afterwards, the as-coated film was heated at 110 \\u00b0C for around 10 min to form a dense CH3NH3PbI3 film.\\nFor the Cs/FA/MA perovskite film, 300.8 mg of PbI2, 35.8 mg of PbBr2 and 70 mg or 140 mg of NMP were dissolved in DMF with the same Pb2+ concentration (1.3 M) at room temperature for the preparation of the precursor solutions. Then the solution was spin-coated on the prepared substrate at 4000 rpm for 25 s. A solution of FAI/MABr in 2-propanol (50 mg mL\\u22121) was spin-coated on the as-prepared film at 4000 rpm for 25 s. The above film was then annealed at 110 \\u00b0C for 10 min to obtain the Cs/FA/MA perovskite film.\\nIn the deposition of the HTL, a spiro-OMeTAD solution was employed with 72.3 mg of spiro-OMeTAD, 28.8 \\u03bcL of TBP and 17.5 \\u03bcL of Li-TFSI solution (520 mg of Li-TSFI in 1 mL of acetonitrile) in 1 mL of chlorobenzene. The spiro-OMeTAD solution was then deposited on the perovskite layer at 4000 rpm for 30 s. Finally, an 80 nm thick Au counter electrode was deposited by thermal evaporation under a reduced pressure of 2 \\u00d7 10\\u22127 Torr. The active area was 0.10 cm2. The whole fabrication procedures were carried out at a relative humidity of \\u223c20%.\\n\\nCurrent\\u2013voltage characteristics were recorded using a solar simulator equipped with a Keithley 2400 source meter and a 300 W collimated Xenon lamp (Newport). The light intensity of the xenon lamp was calibrated to 100 mW cm\\u22122 under AM 1.5 G solar light conditions with a certified silicon solar cell. Incident photon-to-electron conversion efficiency (IPCE) was measured on a computer-controlled IPCE system (Newport) containing a xenon lamp, a monochromator and a Keithley multimeter. The system was calibrated with the certified silicon solar cell and IPCE data were collected in DC mode. XRD patterns were collected using an X-ray diffractometer (Rigaku, RINT-2500) with a CuK\\u03b1 radiation source. Surface morphologies were recorded via a SEM-4800 field-emission scanning electron microscope (SEM). UV-vis spectra were measured for the perovskite films on mesoscopic TiO2 films using a UV-2550 UV-vis spectrophotometer. The steady-state photoluminescence spectra were measured with a CoMPox205 laser device. Electrical impedance spectroscopy and stabilized outputs of current density were measured on a potentiostat CHI 760E. Thermogravimetric analyses were performed using a thermal gravimetric analyzer TG 209F1.\\n\\nDiffraction data were collected using an X-ray single-crystal diffractometer (Agilent Technologies SuperNova system) with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) at 100 K. The data were processed using CrysAlis, and the crystal structure was solved and refined using full-matrix least-squares based on F2 with programs SHELXS-97 and SHELXL-97 within Olex2. The detailed crystallographic data are given in Table S2.\\u2020\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; NMP >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 110.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"9.5 ml hydriodic acid (57% in water, Aldrich) and 5.0 ml cyclopropylamine (98%, Sigma Aldrich) in ethanol (20.0 ml) were reacted in a round-bottom flask of 100 ml at 0 \\u00b0C for 2 h with vigorous stirring. The pure products were obtained after evaporation of reaction solvents and then recrystallized twice from ethanol and diethyl ether. Finally, the products were dried at 60 \\u00b0C in a vacuum oven for 24 h.\\n\\nA solution of 0.14 M PbCl2, 1.26 M PbI2 and 1.3 M MAI in a cosolvent of dimethyl sulfoxide (DMSO) and \\u03b3-butyrolactone (GBL) (vol. ratio = 3:7) was prepared in a glove box. The solution was spin coated on substrates at 1000 rpm for 20 s and then 3500 rpm for 40 s to afford 3D perovskites (MAPbIxCl3\\u2212x) with a slight excess of PbI2. At 45 s, 900 \\u03bcl of anhydrous toluene was dropped on the surface to obtain a smooth film morphology. After the preparation of 3D perovskites, solutions of CAI with various concentrations of 5 mg ml\\u22121, 10 mg ml\\u22121, 20 mg ml\\u22121 and 30 mg ml\\u22121 in anhydrous iso-propyl alcohol (IPA) were spin-coated on the prepared 3D perovskites at 3000 rpm for 30 s and then annealed at 100 \\u00b0C for 20 min to produce 2D perovskites on the top through a reaction of CAI with excess PbI2.\\n\\nTo fabricate the planar perovskite solar cells, a thin layer of PEDOT:PSS was coated on precleaned ITO glass. Then, the photoactive layers, including 2D/3D perovskite hybrids and homogeneous 3D perovskites, were deposited as described above. On the top of the perovskite layer, a PCBM layer of 20 nm was deposited. Next, rhodamine 101 was spin coated with a concentration of 0.05 wt% in IPA at 1500 rpm. Then, a super-thin LiF layer with a thickness of 1.0 nm was evaporated on it. Finally, thermal deposition of a 100 nm thick Ag electrode completed the fabrication of devices.\\n\\nThe current density\\u2013voltage (J\\u2013V) curves were measured by using a solar simulator (XES-50S1, SAN-EI) at 100 mA cm\\u22122 illumination (AM 1.5G) with a scan range from +1.5 V to \\u22120.2 V and a scan rate of 0.1 V s\\u22121, ignoring the hysteresis behavior of conventional PSCs. The hysteresis behaviors of the 2D/3D perovskite hybrid based PSCs were investigated and are given in the ESI.\\u2020 The illumination intensity was calibrated by a Si-reference cell certified by JIS (Japanese Industrial Standards). The J\\u2013V curves of all devices were measured by using an active area of 0.11 cm2. The external quantum efficiency (EQE) was measured by using a power source (QE-LXE 75 W xenon lamp, Enli Technology Co., Ltd) with a monochromator of QE-M110. UV\\u2013vis absorption was measured using a TU-1950 (Beijing's General Instrument Co., Ltd) spectrophotometer. Steady state PL was carried out using a HITACHI F-7000 spectrofluorometer. XRD measurements were performed at room temperature with a PANalytical X'Pert3 powder diffractometer operating in Bragg\\u2013Brentano scanning mode, with an angular resolution of 0.01\\u00b0 and Cu\\u2013K radiation (0.154056 nm wavelength). SEM images were measured by using JSM-7800F. The contact angle test was performed on the Kruss system (Model DSA-10). The thickness of films was tested by using an Alpha-step IQ system.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Rhodamine 101 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO; GBL @ 4; 7 >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Indium tin oxide (ITO) with a sheet resistance of 7 \\u03a9 sq\\u22121 was purchased from CSG Holding Co., Ltd. PbI2 (99.999%), N,N-dimethylformamide (DMF) and dimethyl sulphoxide (DMSO) were purchased from Sigma-Aldrich\\u00ae. Triphenylphosphite (TPPi) was purchased from J&K\\u00ae. CsI (99.999%) and SnI2 (99.99%) were purchased from Sigma-Aldrich\\u00ae. PEDOT:PSS (4083) and PCBM were purchased from Xi'an Polymer Light Technology Corp. (PLT).\\n\\nCsI and SnI2 were dissolved in a DMF:DMSO (volume ratio = 5:1) mixture at a molar ratio of 1:1. The concentration of CsI was 0.5 M. The concentrations of TPPi were 0 vol%, 2 vol%, 4 vol% and 6 vol%. All the solutions were stirred for 12 h on a hot plate at 70 \\u00b0C. In addition, the precursor CsSnI3 QD solutions were prepared by heating on the hot plate at a temperature of 90 \\u00b0C for more than 10 min. The HMR spectra for different solutions were measured using an NMR spectrometer (Bruker AVANCE III HD 400 MHz).\\n\\nThe CsSnI3 films were fabricated on glass substrates. The CsSnI3 solutions were prepared as described above. Each solution was spin-coated on the substrates at a speed of 4000 rpm for 30 seconds. After spin-coating, the precursor films were loaded on a heating station at 90 \\u00b0C for annealing. The morphology of the films was characterized by field emission scanning electron microscopy (FESEM, HITACHI S-4700) and transmission electron microscopy (HRTEM, FEI Tecnai G2 F30). X-ray photoelectron spectroscopy (XPS) was used to study the valence state changes of Sn. XRD measurements were performed to investigate the structures of the crystals. UV-vis absorption spectra were measured using a U-3010 spectrophotometer (Hitachi) instrument. Time-resolved transient photoluminescence (PL) spectra were obtained using a PL spectrometer, FLS 900, Edinburgh Instruments, excited using a picosecond pulsed diode laser (EPL-445) and measured at 405 nm after excitation.\\n\\nPEDOT:PSS (4083) was spin-coated on an ITO substrate at a speed of 3000 rpm for 30 seconds and annealed on a hot plate at 130 \\u00b0C for one hour in an N2 glove box. The CsSnI3 solution with or without TPPi mixture was deposited on top of the PEDOT:PSS layer to produce perovskite films via the process described above. After the perovskite film was formed, an electronic transfer material (15 mg of PCBM in 1 ml of chlorobenzene) was spin-coated on top of the perovskite film at a speed of 1500 rpm for 30 seconds. Finally, a silver (Ag) layer (100 nm) was deposited on top of the PCBM layer via a thermal-evaporation process in a vacuum chamber with a pressure of 5 \\u00d7 10\\u22124 Pa. The typical active area of the devices was approximately 0.12 cm2, which was determined by a shadow mask during the evaporation of the top electrode. The solar light source simulated AM1.5 sun light with an intensity of 100 mW cm\\u22122. The current density (J)\\u2013voltage (V) curves were recorded using a Keithley 2400 source meter unit. The J\\u2013V measurements were carried out in an N2 glove box. The external quantum efficiency (EQE) measurements were carried out using a quantum efficiency (QE)/IPCE measurement system (SR830, Stanford Research Systems). A standard Si photodiode calibrated from Hamamatsu was tested as a reference prior to each sample measurement. Steady-state measurements of the solar cell devices were carried out using an electrochemical workstation (CS150H, Wuhan Corrtest Instruments Corp., Ltd.). Electrochemical impedance spectra (EIS) measurements were obtained using a frequency response analyzer (PSM1735 NumetriQ) from 1 Hz to 106 Hz under dark conditions at 0.1 V applied bias.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsSnI3,\\n Perovskite_composition_short_form: CsSnI,\\n Perovskite_additives_compounds: TPPi,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless stated otherwise, solvents and chemicals were obtained commercially and were used without further purification. PPDIDTT was synthesized according to our previous literature. PC61BM was purchased from American dye Inc. Bphen and PbI2 were purchased from Sigma-Aldrich Inc. N,N-dimethylformide (DMF), dimethylsulfoxide (DMSO) and chlorobenzene (CB) were purchased from Alfar Aesar. Isopropanol (IPA) was purchased from J&K Scientific Ltd. Methylamine (AR, 27% in methanol) was purchased from Sinopharm Chemical Reagent Co. Ltd. Methylammonium iodide (MAI) and methylammonium chloride (MACl) were synthesized according to the previous literature.\\n\\nPerovskite solar cells were fabricated by the following procedure. First of all, an indium tin oxide (ITO) glass substrate (sheet resistance = 15 \\u03a9 \\u25a1\\u22121) was cleaned in an ultrasonic bath of soap water, deionized water, acetone and ethanol for 20 min each, and treated in an ultraviolet-ozone chamber for 20 min. Next, a thin layer (30 nm) of PEDOT:PSS (Baytron PVP AI 4083, Germany) was spin-coated onto the ITO glass at a speed of 4000 rpm for 30 s and annealed at 130 \\u00b0C for 20 min. Then, the MAPbI3\\u2212xClx based perovskite layer was deposited using a sequential deposition method according to the previous literature. 1.25 M PbI2 was dissolved in a mixture solvent of DMF and DMSO (v/v = 9:1) and stirred at room temperature. MAI and MACl (m/m = 9:1) were dissolved in IPA with a total concentration of 30 mg mL\\u22121. The PbI2 solution was spin-coated on the ITO/PEDOT:PSS substrate at a speed of 3000 rpm for 60 s and heated at 70 \\u00b0C to remove the solvent. After cooling down to room temperature, the mixture solution of MAI and MACl was spin-coated onto the PbI2 film at a speed of 4000 rpm for 20 s. The perovskite film was annealed at 85 \\u00b0C for 1 h. PPDIDTT was dissolved in chloroform (CF) with different concentrations (5, 2, 1, 0.5 and 0.2 mg mL\\u22121) and spin-coated on the top of the perovskite film at a speed of 3000 rpm for 30 s. Subsequently, PC61BM (dissolved in CB, 20 mg mL\\u22121) and Bphen (dissolved in IPA, 0.5 mg mL\\u22121) were spin-coated at a speed of 1000 rpm for 60 s and 3000 rpm for 30 s, respectively. Finally, an 80 nm thick Ag counter electrode was deposited on the top of the buffer layer by thermal evaporation at the pressure of 10\\u22126 Torr.\\n\\nUV-vis absorption spectra (ITO/perovskite and ITO/perovskite/PPDIDTT) were measured on a UV-vis spectrophotometer (UV-2550, Shimadzu) with a wavelength ranging from 350 to 850 nm. SEM images (ITO/PEDOT:PSS/perovskite/PPDIDTT/PC61BM/Bphen/Ag) were characterized using a FEI-SEM (XL 30 S-FEG). AFM images (ITO/perovskite, ITO/perovskite/PPDIDTT, ITO/perovskite/PC61BM and ITO/perovskite/PPDIDTT/PC61BM) were obtained using a Multimode 8 scanning probe microscope (Bruker). FTIR spectra (pellets of PPDIDTT, perovskite and PPDIDTT:perovskite) were obtained using a TENSOR27 (Bruker), and Raman spectra (ITO/perovskite, ITO/PPDIDTT and ITO/perovskite/PPDIDTT) were obtained using a JY HR800 spectrometer. TAS (ITO/PEDOT:PSS/perovskite/PPDIDTT/PC61BM/Bphen/Ag) was performed using an IM6ex electrochemical workstation (Zahner), in which the scanning frequency was set between 0.1 and 106 Hz, and the amplitude of the sine perturbation bias was set to 10 mV. The photovoltaic performance was characterized using a Keithley 2602 system source meter and an Oriel Solar Simulator 91192 with irradiation of AM 1.5G, 100 mW cm\\u22122, calibrated with the standard silicon reference cell. When testing, individual devices were masked with a black aperture to confine the active area of the device to 0.1 cm2. EQE spectra were measured using a lab-made spectrometer with a wavelength ranging from 350 to 800 nm. The steady-state PL spectra (SiO2/perovskite/PPDIDTT, SiO2/perovskite/PC61BM and SiO2/perovskite/PPDIDTT/PC61BM and SiO2/perovskite) were measured using the PL spectrometer (Edinburgh Instruments, FLS 900) with Xenon as the excitation source (excitation at 550 nm). The detected emission wavelength of the steady-state PL was from 700 to 850 nm. Time-resolved PL decay transient spectra (SiO2/perovskite/PPDIDTT, SiO2/perovskite/PC61BM and SiO2/perovskite/PPDIDTT/PC61BM and SiO2/perovskite) were obtained using a PL spectrometer (Edinburgh Instruments, FLS 900), excited using a pulsed diode laser (EPL-445, 0.8 mJ cm\\u22122) and measured at 775 nm after excitation at 445 nm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Bphen,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 85.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 60.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO glass was etched with zinc powder and hydrochloric acid (1 M) to house two electrodes, which were cleaned with ultrasonic soap, water, and ethanol bath and then rinsed with deionized water. A 70 nm-thick TiO2 compact layer (cp-TiO2) was deposited on the cleaned FTO substrate by spray pyrolysis of a titanium diisopropoxide bis(acetylacetonate) (75 wt% in isopropanol, Aldrich) precursor solution diluted in ethanol (1:39 v:v) at 485 \\u00b0C for 30 min. This was followed by the deposition of a 20 mM TiCl4 solution layer, which functioned as an electron transport layer (ETL). The mesoporous TiO2 layer (mp-TiO2) was formed by spin-coating a diluted TiO2 solution (1:8.5 v:v) at 4000 rpm for 30 s followed by sintering at 500 \\u00b0C for 30 min. The CH3NH3PbI3 precursor was prepared inside a nitrogen-filled glove box with oxygen and moisture levels <1 ppm by mixing 0.288 g CH3NH3I (dyesol, 99.99%) with 0.831 g PbI2 (Aldrich, 99.999%, ultra-dry) in a 1:1 equimolar ratio. The components were dissolved in a mixture of \\u03b3-butyrolactone (GBL) and dimethyl sulfoxide (DMSO) (6:4 v:v) and heated at 50 \\u00b0C under stirring for 12 h for complete dissolution. CH3NH3PbI3 was then spin-coated on the FTO/cp-TiO2/mp-TiO2 substrate at 1000 rpm for 10 s and at 5000 rpm for 30 s; the anti-solvent toluene was injected for 15 s in the second spin step. The spin-coated perovskite film was dried at 100 \\u00b0C for 10 min to remove toluene. The Spiro-OMeTAD solution was prepared by dissolving 72.3 mg of Spiro-OMeTAD, 28.8 \\u03bcL of tert-butylpyridine (tBP), and 17.5 \\u03bcL of lithium-bis(trifluoromethanesulfonyl)imide (Li-TFSI) (from a stock solution of 520 mg mL\\u22121 of Li-TFSI in acetonitrile (Aldrich, 99.8%)) in 1 mL of chlorobenzene. The Spiro-OMeTAD solution was then spin coated on the MAPbI3 substrate at 4000 rpm for 20 s. An ion beam sputtering system was used to deposit the Cu/Cu2O films. The vacuum chamber was evacuated to a base pressure of 2.2 \\u00d7 10\\u22126 Torr. A copper substrate (99.99% purity) was used as the sputtering target. The Cu/Cu2O films were grown at room temperature (\\u223c30 \\u00b0C) with different Ar and O2 flow rates with working pressure ranging from 1.0 \\u00d7 10\\u22124 Torr to 4.0 \\u00d7 10\\u22124 Torr. Finally, the Cu/Cu2O films were deposited on Spiro-OMeTAD to form the counter electrode. For the device without Cu/Cu2O, a 60 nm-thick silver layer was thermally evaporated on Spiro-OMeTAD as the counter electrode.\\n\\nThe crystallographic properties of the films were determined by grazing incidence X-ray diffraction using Cu-K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5, D8, Bruker, Germany) at room temperature with a scanning step size of 0.005\\u00b0. The surface morphologies and cross-sections of the samples were analyzed by field-emission scanning electron microscopy (SUPRA\\u2122 55). Optical transmittance spectra were obtained using a UV/VIS/NIR Spectrophotometer (HITACHI U4100) at a fixed incidence angle perpendicular to the film surface in the range of 300\\u2013900 nm. The FTO glass was used as a reference for transmittance measurements. The carrier type, carrier concentration, and electrical resistivity were measured using a four-terminal van der Pauw configuration at room temperature. The UPS experiment was performed at beamline 24A of the Taiwan Light Source at the National Synchrotron Radiation Research Center (NSRRC). A microscopic PL system (MRI, Protrustech Co., Ltd, Taiwan) was used to determine the band gap of the films with a pump wavelength of 532 nm. The J\\u2013V measurement was performed using a solar simulator (SS-F5-3A, Enlitech) with AM 1.5G spectrum, and the device was connected to a source meter (Keithley 2401) to obtain the J\\u2013V data. The light intensity was calibrated to be 100 mW cm\\u22122 using reference silicon solar cells. The scan rate was 0.14 V s\\u22121 for the forward scan (from Jsc to Voc). A metal mask with an aperture size of 0.09 cm2 was used to define the active area. A 300 W intensity monochromatic (Newport Cornerstone 260) xenon lamp (Newport) and a source meter (Keithley 2401) were integrated to measure the IPCE responses of the devices.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Cu; Cu2O,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Sputtering,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide, lead chloride, titanium diisopropoxide bis(acetylacetonate) (75% in isopropanol), and N,N-dimethylformamide were purchased from Alfa Aesar. Chlorobenzene was purchased from Acros. Spiro-MeOTAD was purchased from Lumtec. CH3NH3I was prepared using the method reported in literature. The conventional transparent conductive oxide substrate was FTO (Pilkington, thickness: 3.2 mm, sheet resistance 10 \\u03a9 per square). Cd2SnO4 thin films used as solar cell substrates were deposited by radio frequency magnetron sputtering on corning glass (sheet resistance: \\u223c10 \\u03a9 per square).\\n\\nThe devices Cd2SnO4 (and FTO)/bl-TiO2/mp-TiO2/CH3NH3PbI3\\u2212xClx/spiro-OMeTAD/Au were fabricated. First, the transparent conductive oxide substrates were cleaned with a detergent. They were then sonicated with high purity water in an ultrasonic bath for 15 min, and finally placed in boiling water for 5 min, and the abovementioned steps were repeated three times. TiO2 blocking layer (bl-TiO2) of 40 nm was prepared by spray pyrolysis using titanium diisopropoxide bis(acetylacetonate) (75% in isopropanol) (diluted in ethanol in a volumetric ratio of 1:40) at 450 \\u00b0C. To prepare a 120 nm mesoporous TiO2 layer (mp-TiO2), diluted 18NR-T (Dyesol 18NR-T:ethanol = 2:15, m/m) was spin coated on the substrate at 4200 rpm for 40 s, and then annealed at 500 \\u00b0C for 60 min. CH3NH3I was mixed with PbI2 and PbCl2 (mole ratio of PbI2:PbCl2:CH3NH3I = 1:1:4, 50 wt%) in DMF. Stirring at 65 \\u00b0C and filtration led to transparent precursor solution. To obtain CH3NH3PbI3\\u2212xClx films, the precursor solution was spin-coated on the mp-TiO2 layer at 4000 rpm for 50 s, and then placed in a drying cabinet for 50 min (at 20% relative humidity), followed by thermal annealing at 100 \\u00b0C for 75 min. The spiro-MeOTAD layer was spin coated on the perovskite layer at 2000 rpm for 30 s from a hybrid solution (dissolved in chlorobenzene, 72 mg/1 mL; 17 \\u03bcL Li-bis(trifluoromethanesulfonyl)-imide (Li-TFSI), dissolved in acetonitrile, 520 mg mL\\u22121 and 20 \\u03bcL tert-butylpyridine (t-BP)). The gold film of 100 nm was deposited on the spiro-MeOTAD layer as the back electrode by thermal evaporation technology.\\n\\nThe transmittance spectra were obtained using a Perkin Elmer Lambda 950 Spectrometer. The ultraviolet photoelectron spectroscopy (UPS) measurements of Cd2SnO4 film were performed using Thermo Scientific Escalab 250Xi. The SEM images were obtained using a Hitachi S-5200. Atomic force microscopy (AFM) measurements of the samples were conducted using Bruker multimode 8 scanning probe microscopy. The photo I\\u2013V curves were obtained using a Keithley 2400 Source meter under simulated AM 1.5G sunlight irradiation (100 mW cm\\u22122) (ABET technologies Sun 2000 solar simulator). The light intensity was calibrated using a GaAs reference cell certificated by NREL. The dark I\\u2013V curves were obtained using an Agilent 4284A precision LCR meter. The external quantum efficiency (EQE) was measured using a QEX10 measurement system (PV Measurements, Inc.). The active area of the devices was typically 0.15 cm2. The steady-state and time-resolved photoluminescence spectra were obtained using a FLS 980 fluorescence spectrometer (Edinburgh Instruments) with excitation at 655 nm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 75,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned indium tin oxide (ITO) glass substrates (15 ohm \\u25a1\\u22121) were supplied by NSG group. Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS, Clevios P VP Al 4083) was purchased from Heraeus Holding GmbH. Methylammonium iodide (MAI) was obtained from Dyesol Ltd. [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) was bought from Nano-C Inc. Other materials, including lead(II) iodide (PbI2, 99% and 99.999% purity), dimethyl sulfoxide (DMSO, anhydrous, \\u226599.9% purity), \\u03b3-butyrolactone (GBL, \\u226599% purity), LiF (\\u226599% purity), chlorobenzene (anhydrous, 99.8% purity) and toluene (anhydrous, 99.5% purity), were supplied by Sigma-Aldrich. All materials are used without further purification.\\n\\nITO glass substrates were cleaned sequentially by sonication in detergent, deionized water, acetone, and isopropanol for 20 min each. After drying under a N2 stream, substrates were further treated with UV-ozone for 15 min. A PEDOT:PSS (Baytron 4083 filtered through a 0.45 \\u03bcm filter) hole transporting layer with a thickness of \\u223c40 nm was spin-coated onto ITO substrates at 6000 rpm for 40 s and annealed at 150 \\u00b0C for 15 min in air. The substrates were then transferred into a N2 filled glovebox, and spin coated with prepared different precursor solutions containing 1.4 M PbI2 and 1.4 M MAI in the co-solvent of DMSO:GBL (3:7 vol. ratio) at 1000 rpm for 20 s, and washed with toluene after 20 s at 5000 rpm. Then the substrates were annealed at 100 \\u00b0C for 15 min. The thickness of the perovskite thin films is around 260 nm, determined by using a surface step profiler. The electron-transporting layer (PCBM, 20 mg mL\\u22121 in chlorobenzene) was then deposited by spin coating at 2000 rpm for 1 min. The LiF (0.5 nm) interlayer and Al (100 nm) electrodes were deposited under high vacuum (<1 \\u00d7 10\\u22126 Torr) through a shadow mask, defining a device area of 0.11 cm2, by thermal evaporation. The SCLC device was fabricated with a configuration of ITO/PEDOT:PSS/MAPbI3/MoO3/Ag for the hole only device, and ITO/PEI/MAPbI3/PCBM/LiF/Al for the electron only device. All J\\u2013V curves were recorded using a Keithley 2400 source meter unit. The device photocurrent was measured under AM 1.5 illumination condition at an intensity of 100 mW cm\\u22122 which was accurately calibrated using a standard Si photodiode detector. The IPCE spectra studied here were obtained from an IPCE setup consisting of a Xenon lamp (Oriel, 300 W) as the light source, a Cornerstone 260 Oriel 74125 monochromator, a lock-in amplifier (SR830, Stanford Research Corp), and a Si-based diode (J115711-1-Si detector) for calibration.\\n\\nX-ray diffraction (XRD) patterns were acquired using a Bruker D8 Advance XRD Instrument. Absorption spectra were recorded on a Shimadzu UV-1800 spectrophotometer. Electron scanning microscopy (SEM) images were obtained with a Zeiss Supra-40 SEM. Film thickness was determined by using a surface profilometer (KLA Tencor, Alpha-Step IQ). Photoluminescence spectra were obtained on a LS 55 Fluorescence Spectrometer (PerkinElmer) with an excitation wavelength of 410 nm. Time-resolved photoluminescence: the excitation source is a diode laser (NanoLED) working at a repetition rate of 10 MHz, with a wavelength of 438 nm and a pulse duration of \\u223c260 ps. The scattering of excitation light was eliminated by using a two 600 nm long pass filter. Photoluminescence is collected and detected by using an avalanche photon diode (Micro photon device, PicoQuant) attached to a time-correlated single photon counting card (TCSPC PicoHarp 300, PicoQuant).\\nFemtosecond transient absorption: the laser pulses generated from a mode-locked Ti:sapphire oscillator seeded regenerative amplifier working at 800 nm with a repetition rate of 1 kHz and a pulse duration of 50 fs. The 800 nm laser was split into two portions. An optical parametric amplifier (TOPAS, Light conversion) was pumped by one portion (with an average power of 1 W) of this 800 nm laser. The generated beam with a wavelength of 500 nm serves as the \\u201cpump\\u201d in the typical pump\\u2013probe scheme. The residual portion of the 800 nm laser pulses generated a white light continuum in a 1 mm sapphire plate. The fluctuation of both pump and probe beams was cancelled out. The pump beam was focused onto the film with a beam size of 300 \\u03bcm and overlapped with a smaller diameter probe beam, \\u223c100 \\u03bcm. The time delay of the pump and probe laser pulses was varied by using a computer controlled translational stage (Newport, ESP300). The pump beam was modulated by using an optical chopper at a frequency of 500 Hz. The variation transmittance at a selected probe wavelength was recorded as a function of time delay between pump and probe pulses.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Initially, laser-patterned, ITO- and FTO-coated glass substrates (TEC15, Pilkington) were cleaned by ultrasonication in an alkaline, aqueous washing solution, and then rinsed with deionized water and ethanol. The PET/ITO substrates were cleaned only with detergent and ethanol. TiO2 thin films of different thicknesses were fabricated using radio frequency (RF) magnetron sputtering on a flexible indium-doped tin oxide (ITO)-coated conducting glass and/or PET substrates with a sheet resistance of 20 \\u03a9 cm\\u22122. A pure titanium metal target (Ti) with an area of 2 cm2 and 99.99% purity was used for sputtering. The sputtering chamber was initially evacuated to 2.2 \\u00d7 10\\u22126 Torr and then maintained at 10 mTorr by flowing Ar and O2 gases during sputtering. During deposition, the Ar to O2 gas flow rate ratio was set to 8:2 (20% oxygen). The samples were deposited at room temperature with an applied power of 130 W. TiO2 films with three thicknesses of 30, 50 and 100 nm were grown by adjusting the sputtering time and using a quartz thickness monitor placed close to the substrates in the sputtering chamber. The growth rate of the TiO2 film was 0.5 \\u00c5 per cycle.\\nThe highly uniformly deposited Bl-TiO2 layers on glass/ITO and PET/ITO substrates with different thicknesses (30, 50 and 100 nm) using RF magnetron sputtering at room temperature have been used as an alternative ETL to the conventional methods. The deposited PET/ITO/Bl-TiO2 and/or glass/ITO/Bl-TiO2 substrates were transferred into a nitrogen filled glove-box for MAPb(I3\\u2212xBrx)3 perovskite deposition. Second, a desired mixture of MAI, MABr, PbI2, or PbBr2 in GBL and DMSO solvent was dripped onto the PET/ITO/Bl-TiO2 (1.5 \\u00d7 1.5 cm2) surface. This substrate was then spun in a spin-coater at speeds of 1000 rpm (10 s) and 4000 rpm (40 s). Third, a solvent that is immiscible with the perovskite materials, such as toluene, was dripped onto the substrate during spin coating. Fourth, the uniformly deposited MAPb(I1\\u2212xBrx)3 thin film was dried on a hot plate to obtain crystalline MAPb(I1\\u2212xBrx)3 perovskite materials. Fifth, the HTM material (PTAA) from the toluene solution was spin-coated at 3000 rpm at room temperature. Finally, the device was completed by the deposition of an 80 nm thin Au contact using thermal evaporation.\\n\\nAll chemicals for the preparation of the flexible perovskite solar cells were of reagent grade and were used without further purification. In the present case, we have also used three different types of ETL electrodes. The first is Bl-TiO2 processed at high temperature (non-flexible PSC) and the second is TiOx formed by the sol\\u2013gel process (flexible PSC) for comparison. Compact TiO2 layers of approximately 50 nm thick were deposited on the FTO substrates by spin coating of 0.15 M and 0.3 M commercial titanium diisopropoxide bis(acetyl acetonate) solution (75% in 2-propanol, Sigma-Aldrich) diluted in ethanol (1:39, volume ratio) as the precursor and subsequently annealed in air at 450 \\u00b0C for 30 min. The sol\\u2013gel synthesis of TiOx was performed as per the previous literature with few modifications. Briefly, titanium(IV) isopropoxide (Ti[OCH(CH3)2]4, Aldrich, 99.999%, 10 ml) was prepared as a precursor and mixed with 2-methoxyethanol (CH3OCH2CH2OH, Aldrich, 99.9+%, 50 ml) and ethanolamine (H2NCH2CH2OH, Aldrich, 99+%, 5 ml) in a three-necked flask equipped with a condenser, a thermometer, and a nitrogen-gas inlet/outlet. Then, the mixed solution was heated to 80 \\u00b0C for 2 h with magnetic stirring followed by heating to 120 \\u00b0C for 1 h. The two-step heating (80 and 120 \\u00b0C) was then repeated. The typical TiOx precursor solution was prepared in isopropyl alcohol and spin cast onto PET/ITO substrates.\\n\\nMethylammonium lead iodide (MAPbI3) and methylammonium lead bromide (MAPbBr3) were synthesized as per our previous reports. The CH3NH3I (MAI) and CH3NH3Br (MABr) were first synthesized by reacting 27.86 ml methylamine (CH3NH2) (40% in methanol, Junsei Chemical) and 30 ml hydroiodic acid (HI) (57 wt% in water, Aldrich) or 44 ml hydrobromic acid (HBr) (48 wt% in water, Aldrich), respectively, in a 250 ml round-bottom flask in an ice cold solution for 2 h with stirring, followed by solvent evaporation using a rotary evaporator (95 mbar vacuum, 400 rpm rotation) at 60 \\u00b0C. The resulting white solid product MAI/MABr was dissolved in ethanol and recrystallized using diethyl ether. The fresh fine white crystals were washed three times using diethyl ether and then dried in a vacuum for 24 h. The MAPb(I1\\u2212xBrx)3 perovskite solution was prepared by dissolving the desired amounts of MAI, MABr, lead iodide (PbI2) and lead bromide (PbBr2) (Aldrich, 99.999%) in anhydrous \\u03b3-butyrolactone (GBL) in dimethyl sulfoxide (DMSO) (Sigma-Aldrich) (7:3 v/v) at 60 \\u00b0C overnight. The clear filtered yellow solution was spin coated on the top of the Bl-TiO2 samples by a consecutive two-step spin-coating process at 1000 and 5000 rpm for 10 and 40 s, respectively. One drop of toluene was drop-cast during the second spin-coating step followed by a heat treatment on a hot plate for 10 min to form dark-brown colored crystalline MAPb(I1\\u2212xBrx)3. The hole transport material (HTM) was prepared by the standard procedure reported elsewhere. 15 mg poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA, EM Index, Mw = 17500 g mol\\u22121) in toluene (1.5 ml) was mixed with 15 \\u03bcl of a solution of bis(trifluoromethane)sulfonimide lithium salt (LiTFSI, 99.95%, Aldrich) (170 mg cm\\u22121) in acetonitrile (1 ml) and 7.5 \\u03bcl 4-tert-butylpyridine (TBP, 96%, Aldrich) and spin-coated on the glass/ITO/Bl-TiO2/MAPb(I1\\u2212xBrx)3 substrate at 3000 rpm for 30 s. Then, the substrates were transferred to a vacuum chamber and subsequently evacuated to a pressure of 2 \\u00d7 10\\u22126 mbar. For the Au counter electrode, an 80 nm-thick Au layer was deposited on the top of the HTM over layer by thermal evaporation (growth rate approximately 0.5 \\u00c5 s\\u22121) at a pressure of 2 \\u00d7 10\\u22126 mbar. The active areas of all devices were 0.03 cm2.\\n\\nHigh resolution X-ray diffraction (HRXRD) measurements were carried out using a D/MAX Ultima III XRD spectrometer (Rigaku, Japan) with the Cu K line at 1.5410 \\u00c5. The cross-sectional images were recorded by using a field emission scanning electron microscope (FESEM; S-4700, Hitachi). The cells were illuminated using a solar simulator at AM 1.5 G for 10 s, for which the light intensity was adjusted to 1 sun intensity (100 mW cm\\u22122) through the use of an NREL-calibrated Si solar cell with a KG-5 filter. The IPCE spectra were measured as a function of wavelength from 300 to 900 nm using a Spectral Products DK240 monochromator. All IPCE spectra were normalized to the measured J\\u2013V current for accurate comparison. The IPCE data were collected in the constant energy DC mode with a delay time of 10 ms and a light intensity of 50 \\u03bcW cm\\u22122. Solid state impedance spectroscopy (ssIS) was conducted using an IviumStat (Ivium Technologies B.V., Eindhoven, the Netherlands) under open-circuit conditions at frequencies ranging from 10\\u22121 to 105 Hz with an AC amplitude of 10 mV. Z-view 2.8d (Scribner Associates) was used to fit the IS spectra to the equivalent circuit based on the transmission line model. The DC bias potential was applied in 0.05 V step intervals.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbBrI2,\\n Perovskite_composition_short_form: MAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.03,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Tin (IV) oxide (SnO2, 15% in H2O colloidal dispersion), Dimethyl sulphoxide (DMSO), chlorobenzene (CB) and N, N-dimethylformamide (DMF) were purchased from Alfa Aesar. CH3NH3I (MAI, 95%) and lead iodide (PbI2, 99.9%) were obtained from Xi'an p-OLED. 2, 2\\u2032, 7, 7\\u2032-tetrakis (N, N-di-p-methoxyphenylamine)-9, 9\\u2032-spirobifluorene (Spiro-OMeTAD, 99.5%) was supplied by Weihua Solar. Fluorine-doped tin oxides (FTO) glass with a resistivity of 12\\u202fV\\u202fcm\\u22122 was purchased from Wuhan GeAo Corporation Ltd. Deionized water with a resistivity of 18.3\\u202fM\\u03a9\\u202fcm was used in the whole preparation. Other reagents (containing TiCl4 solution and alcohol) were received from Sinopharm Chemical Reagent Corporation, Ltd.\\n\\nThe FTO substrates were selectively etched in diluted HCl aqueous solution, with moderate Zn powder added in it. The etched substrates were carefully cleaned by foamless eradicator and then were degreased by sonication in water, deionized water, acetone, ethanol, respectively, followed by blow-dried by nitrogen gas and cleaned by UV-ozone cleaning system for 15\\u202fmin. The TiO2 monolayer ETLs were prepared by a chemical bath deposition process. Briefly, the FTO substrates were immersed in a beaker filled with 0.05\\u202fM titanium tetrachloride (TiCl4) aqueous solution, which was then kept at 70\\u202f\\u00b0C for 1\\u202fh in a water bath, resulting in the formation of TiO2 films on the FTO substrates. After the deposition of TiO2 films, the TiCl4-treated FTO subtracts were washed thoroughly with deionized water and alcohol, followed by blow-dried by nitrogen gas and baked on a hot plate at 130\\u202f\\u00b0C in air for one hour and then cooled down to room temperature in air. The as-prepared samples were named as TiO2 samples.\\nA blocking layer of compact SnO2 was formed by spin-coating a SnO2 nanoparticles precursor, which was obtained from Alfa Aesar and was diluted with water (the mass ratio of the purchased SnO2 solution and water was 1:5) before use. The precursor solution was then spin-coated onto the cleaned FTO substrates at 3000\\u202frpm for 30\\u202fs. Subsequently, the samples were baked on a hot plate at 150\\u202f\\u00b0C in air for 30\\u202fmin and then cooled down to room temperature in air. The as-prepared samples were named as SnO2 samples.\\nThe TiO2-SnO2 bilayered films were obtained by spin coating the SnO2 nanoparticles precursor solution onto the prepared TiO2 samples directly. All the treatment was exactly same with the monolayer film deposition. The as-prepared samples were named as TiO2-SnO2 samples.\\n\\nDevices with the n-i-p planar structure of FTO-ETL-MAPbI3-Spiro-OMeTAD-Ag were fabricated by using three different ETLs including TiO2, SnO2 and TiO2-SnO2 films. The ETL coated substrates (TiO2 samples, SnO2 samples and TiO2-SnO2 samples) were transferred into a nitrogen filled glove box to deposit perovskite films and HTLs. The perovskite precursor solution was prepared by dissolving 2.8\\u202fg of PbI2 and 1.0\\u202fg of CH3NH3I in a 1.5\\u202fmL of DMSO and 3.5\\u202fmL of DMF mixed solution, followed by being stirred at 70\\u202f\\u00b0C overnight and then filtered through TPFE filter (0.45\\u202f\\u03bcm) before use. An anti-solvent method reported in our previous report [38] was conducted to achieve high performance perovskite films. The perovskite precursor solution was dropped onto the ETL coated substrates, and then spin-coated at a low speed of 1000\\u202frpm for 5\\u202fs and a sequential high speed of 3000\\u202frpm for 30\\u202fs, respectively, during which 130\\u202f\\u03bcL of chlorobenzene was dripped onto the films 15\\u202fs prior to the ending. Then the wet films were baked at 100\\u202f\\u00b0C for 10\\u202fmin in the glove box. The HTL was spin-coated onto the perovskite layers at 1500\\u202frpm for 45\\u202fs from a Spiro-OMeTAD solution. The specific stoichiometric ratio of the Spiro-OMeTAD solution could be described as follows: 72.3\\u202fmg Spiro-OMeTAD was added in 1\\u202fmL chlorobenzene, with the addition of 17.5\\u202f\\u03bcL Li-TFSI/acetonitrile (520\\u202fmg\\u202fmL\\u22121) solution and 28.8\\u202f\\u03bcL tBP. Finally, all of the samples were carried out of the glove box and the device was completed by evaporating a silver counter electrode on the Spiro-OMeTAD layer. The active area for each device was fixed at 0.07\\u202fcm2 by overlaying customized mask on the Spiro-OMeTAD film during the vacuum thermal evaporation.\\n\\nA transmission electron microscopy (TEM, JEM-2010, JEOL Inc., Japan) was employed to characterize the microstructural and crystalline properties of the SnO2 nanoparticles. X-ray diffraction (XRD) analysis was employed to characterize the crystalline properties of the SnO2 nanoparticles and MAPbI3 films, using a D/max-2400 X-ray diffraction spectrometer (XRD, Rigaku, Japan) with Cu Ka radiation and operated at 40\\u202fkV and 100\\u202fmA. The scanning speed was 5\\u00b0\\u202fper minute at the step of 0.02\\u00b0. X-ray photoelectron spectroscopy (XPS, AXIS Ultrabld, Kratos) was employed to characterize the element composition of the SnO2 nanoparticles. The surface morphologies of the samples were characterized by a scanning electron microscopy (SEM, JSM-6390, JEOL Inc., Japan). The topographic images of the sample were obtained by using an atomic force microscope (AFM, Innova Atomic Force Microscope, Santa Barbara, CA USA) in trapping mode. The absorption and transmission spectra of the samples were acquired by a JASCO V-570 UV/vis/ NIR spectrometer.\\nAll the following measurements were tested in ambient environment. The J-V curves measurements of the devices were conducted 24\\u202fh after the vacuum thermal evaporation by a PVIV-201\\u202fV I-V Station (Newport Oriel) The illumination source was calibrated by using a Si reference cell system (91150\\u202fV, Newport) before use. All the J-V curves were obtained at a scanning speed of 200\\u202fmV\\u202fs\\u22121 from 1.2\\u202fV to \\u22120.1\\u202fV. Electrochemical impedance spectroscopy (EIS) measurements were carried out on a CHI660E electrochemical workstation (Chenhua, Shanghai) under one sun illumination (AM 1.5\\u202fG, 100\\u202fmW\\u202fcm\\u22122), with a small perturbation of AC at 5\\u202fmA and a frequency range between 1\\u202fMHz and 10\\u202fHz. External quantum efficiency (EQE) spectra of the devices were obtained by using a Qtest Station 1000ADX system (Growntech, Inc.).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals were used as received, including titanium diisopropoxide bis(acetylacetonate) (75\\u00a0wt % in isopropanol, Sigma-Aldrich), 1-butanol (99.8%, Sigma-Aldrich), titanium oxide (TiO2) paste (Dyesol 18NR-T), PbI2 (99.9983%,Sigma-Aldrich), N,N-dimethylformamide (DMF, anhydrous 99.5%, Sigma-Aldrich), lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI, Sigma-Aldrich), spiro-MeOTAD (99%, Shenzhen Feiming), chlorobenzene (SigmaAldrich), acetone, ethanol, acetonitrile.\\nThe morphological characteristics of the thin films were observed by scanning electron microscopy (SEM) in a JEOL JCM-6000 and a Hitachi SU-8020. X-ray diffraction (XRD) was employed to characterize the crystallinity of the films using an XRD Bruker D2 phaser. The UV\\u2013Vis transmission spectra were characterized by using a scientific evolution 300 Spectrometer.\\n\\nFluorine doped Tin Oxide (FTO) glass was patterned by chemical etching with Zinc (Zn) powder and chloride acid (HCl) solution. The etched substrate was then cleaned with hellamanex 2% and ultrasonically cleaned with 2-propanol and deionized water in sequence for 15\\u00a0min, respectively. Afterward, the substrates were further cleaned using O2 plasma cleaning for 15\\u00a0min. A dense layer of TiO2 was then coated on the substrates by spin coating of titanium diisopropoxide bis(acetylacetone) (75\\u00a0wt% in isopropanol, Aldrich) diluted in absolute ethanol (v/v, 1/20) at 3000\\u00a0rpm for 1\\u00a0min. The substrates were then heated at 180\\u00a0\\u00b0C by 5\\u00a0min followed by annealing at 450\\u00a0\\u00b0C for 1\\u00a0h. A mesoporous layer of TiO2 was then deposited by spin-coating TiO2 paste (Dyesol 18NR-T) diluted in absolute ethanol at 1:12\\u00a0wt ratio at 5000\\u00a0rpm for 30\\u00a0s. The substrates were then heated at 180\\u00a0\\u00b0C for 5\\u00a0min, followed by annealing at 450\\u00a0\\u00b0C for 1\\u00a0h. For the fabrication of the standard cell, the methodology proposed by Sutanto et\\u00a0al., 2017 [], was followed, using DMF as solvent. Previously prepared solution 1.25\\u00a0M of PbI2: MAI with a 1: 1\\u00a0M ratio and left at 70\\u00a0\\u00b0C for 12\\u00a0h MAPbI3 solution was deposited by spin-coating on the mesoporous layer of TiO2 at 5000\\u00a0rpm for 30\\u00a0s. After 4\\u00a0s of having started the centrifugation technique, 400\\u00a0\\u03bcL of chlorobenzene were rapidly added to the substrate. Furthermore, a hole transport material (HTM) of Spiro-OMeTAD was spin-coated at 3000\\u00a0r.p.m. for 30\\u00a0s from a chlorobenzene solution (79.1\\u00a0mg in 690\\u00a0\\u03bcL) that contained 22\\u00a0\\u03bcL of 4-tert-butylpiridine and 15\\u00a0\\u03bcL of Li-TFSI (Bis(trifluoromethane)sulfonimide lithium salt) from a 500\\u00a0mg/ml stock solution in acetonitrile as dopants (Fig.\\u00a02 ).\\nTo study the effect of Im+1 on MAPbI3 on the performance of the photovoltaic device, Im+1 was incorporated in a different stoichiometric ratio. The perovskite film was deposited also by spin coating a previously prepared solution 1.15\\u00a0M of MAI:PbI2 with a 1:1\\u00a0M relation in a solvent mixture of DMF/DMSO (80:20 v/v) by a one-step process at 3000\\u00a0r.p.m. for 30\\u00a0s. After a 6\\u00a0s delay time of the spin coating process, a 650\\u00a0\\u03bcL of anhydrous chlorobenzene were added on top of the substrate. Additionally, perovskite thin films were sintered at 100\\u00a0\\u00b0C for 10\\u00a0min. HTM was spin coated at 3000\\u00a0rpm for 30\\u00a0s. Finally, an 80\\u00a0nm thick silver counter electrode was deposited under high vacuum by physical vapor deposition.\\n\\nThe J-V curves were measured using a solar simulator (Newport, Oriel Instruments, 91160\\u00a0A) with a source meter (Keithley 2400). In addition, a Xenon lamp was used as a light source and the illumination source was calibrated using a silicon reference solar cell (enlitech) to calibrate the output power of the lamp to 1000\\u00a0W/m2.\\nThe measurements were performed inside the glove box in order to protect the stability of the cells. The cell area was limited using a metal mask (2.54\\u00a0\\u00a0mm\\u00a0\\u00d7\\u00a02.54\\u00a0\\u00a0mm). The active area of device is 0.65\\u00a0mm2.\\n\\nInitially a purification of the HI (Iodhydric acid) solution was carried out; a 0.36\\u00a0M solution of tributyl phosphate in chloroform was prepared, and a liquid-liquid extraction was carried out in a separating funnel. For crystallization, 10\\u00a0ml of HI solution was used, and 0.9412\\u00a0g of imidazole was dissolved, the mixture was poured into a crystallizer and slow evaporation was prevented. The iodine crystals were recrystallized with ethanol and anhydrous diethyl ether.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.65,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (99.999% trace metals basis), ammonium fluoride (NH4F) (\\u226599.99% trace metals basis), ammonium chloride (NH4Cl) (99.99% trace metals basis), ammonium bromide (NH4Br) (99.999% trace metals basis), ammonium iodide (NH4I) (99.999% trace metals basis), dimethyl sulfoxide (DMSO), \\u0263-butyrolactone (GBL) and chlorobenzene (CB) were purchased from Sigma-Aldrich. Methylammonium iodide (MAI) was purchased from DyeSol and all the materials were used as received without any further purification. To prepare the perovskite precursor solution, we mixed MAI (159 mg) powder and PbI2 (461 mg) (1:1 molar ratio) in 1 mL mixed GBL:DMSO (0.7:0.3) solvent for the reference perovskite precursor solution. Whereas, for the NH4X (X = F, Cl, Br, I) incorporated MAPbI3 perovskite solution, 0.10 M of NH4F (3.70 mg), NH4Cl (5.34 mg), NH4Br (9.79 mg) and NH4I (14.49 mg) were added in the reference perovskite precursor solution. All perovskite precursor solutions were kept for stirring at 70 \\u00b0C for overnight before use. The important point here to be noted is that the solubility of NH4F is very low. Although, we added very small amount (3.70 mg) in 1 mL reference perovskite precursor solution but it was not well soluble and need to filter to remove the insoluble NH4F. Whereas, other ammonium halide materials showed good solubility with given quantities.\\n\\nFor inverted planar perovskite solar cells device fabrication, firstly, the patterned glass/ITO substrates were cleaned with DI water, acetone and isopropanol and dried in drying oven at 140 \\u00b0C for overnight. PEDOT:PSS (Clevios P VP AI4083) was spin-coated on UV-ozone treated glass/ITO substrates at 4000 rpm for 60 s in air and dried at 150 \\u00b0C for 20 min. Then, the samples were transferred to the N2 filled glove-box for further device fabrication steps. Perovskite precursor solution without and with NH4X (X = F, Cl, Br, I) was spin coated in N2 filled glove-box at 2000 rpm for 60-70 s, followed by a step of 1000 rpm for 20 s. During the 2nd step of 2000 rpm for 60 s, a chlorobenzene (CB) solution (400 \\u03bcL) was dropped on the substrate during spin coating after 40 s and continued the spin for further 20 s. The important point to be noted here that the CB dripping time during 2nd spin-coating step was further delayed approximately 5 to 10 s for NH4X (X = F, Cl, Br, I) containing perovskite precursor solutions as compare to reference solution. Then, the samples were dried on hot plate at 100 \\u00b0C for 3 min. Then PC61BM (purchased from OSM, Republic of Korea) as ETL was deposited on the glass/ITO/ PEDOT:PSS/perovskite substrate by spin coating PC61BM (20 mg/1 mL in CB) solution at 1200 rpm for 30 s followed by a final spin-coating step of 2000 rpm for 2 s. Finally, the LiF/Al (0.5 nm/100 nm) electrode was deposited by thermal evaporation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: NH4F,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 3,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The material CH3NH3I (MAI) was synthesized based on the literature . In short, to prepare MAI, hydroiodic acid (10\\u00a0mL, 57\\u00a0wt % in water, Sigma\\u2013Aldrich) and methylamine (10\\u00a0mL, 33\\u00a0wt% in absolute ethanol, Sigma\\u2013Aldrich) were reacted in a round bottomed flask in ice-cold water with stirring for 60\\u00a0min. Raw MAI was obtained by removing the solvent at 50\\u00a0\\u00b0C on a rotary evaporator. The material was then washed in diethyl ether and filtered several times. The precipitate was then dried in vacuum oven overnight at 50\\u00a0\\u00b0C and kept in nitrogen-filled glove box.\\n\\nITO-coated glasses (7\\u00a0\\u03a9/\\u25a1 sheet resistivity) were patterned by etching with a laser to remove 1/3 electrode area, which aims to prevent the short circuit between underlying ITO electrode and the contact point for current\\u2013voltage measurement. Before deposition of other films, the ITO-coated glass substrates were ultrasonically cleaned with detergent, deionized water, acetone and ethanol sequentially, and then were blow-dried in nitrogen. After that, PEDOT:PSS solution (Clevious Al 4083) was spin-coated on ITO-coated substrates at 2000\\u00a0r.p.m for 45\\u00a0s, and then the PEDOT:PSS films were annealed at 150\\u00a0\\u00b0C for 20\\u00a0min. After cooling down, perovskite precursor solutions were spin-coated on PEDOT:PSS films at 3000\\u00a0r.p.m for 45\\u00a0s. The precursor solutions were prepared by mixing PbCl2 (or/and PbI2) (Alfa Aesar) and MAI in N,N-dimethylformamide (DMF, Sigma\\u2013Aldrich). Note that the weighing and dissolution of MAI and lead halide materials were both done in the nitrogen-filled glove box. The spin-coated perovskite films were then annealed at 100\\u00a0\\u00b0C for 90\\u00a0min on a hot plate. 20\\u00a0mg\\u00a0ml\\u22121 PCBM (FEM. Inc.) solution in chlorobenzene (Sigma\\u2013Aldrich) was then spin-coated at 1000\\u00a0r.p.m for 45\\u00a0s. Finally, Ag metal layer was deposited by evaporation through an aperture mask to complete the devices with ITO/PEDOT:PSS/Perovskite/PCBM/Ag planar structure. The active device area is about 0.12\\u00a0cm2. This device structure can provide significant advantage of low-temperature processing, which enables the application of perovskite solar cells in a broader range of substrates . Steady-state photoluminescence (PL) measurement was carried out to study the compatibility of the PEDOT:PSS and PCBM with perovskite film. A considerable decrease in PL intensities (Fig.\\u00a0S1) could be found when perovskite film contacts with PEDOT:PSS or PCBM film, indicating PEDOT:PSS and PCBM can act as exceptional hole and electron acceptors, respectively, to collect photogenerated species in MAPbI3-xClx absorber.\\n\\nX-ray diffraction (XRD) analysis was performed on a D/max-RB diffractometer (Rigaku) using Cu Ka radiation at a scan rate of 6\\u00b0\\u00a0min\\u22121. Steady-state photoluminescence (PL) spectra were measured using an excitation wavelength of 600\\u00a0nm in an Edinburgh FLS 920 spectrophotometer equipped with a Xe lamp and monochromator. The energy-dispersive X-ray (EDX) compositions and spectra were performed using energy-dispersive spectroscopy (EDS) combined with a field-emission scanning electron microscope (SEM, Hitachi S4500). SEM images were obtained using Hitachi S4500 and Hitachi S5200. Film absorbance spectra were measured by Shanghai UV\\u2013vis SP-752 spectrometer. Current-voltage measurements and power conversion efficiencies were obtained using Keithley 2400\\u00a0at room temperature under AM 1.5G illuminations (1000\\u00a0W\\u00a0m\\u22122) from a solar simulator which was calibrated using a standard silicon solar cell device. The IPCE spectra were performed on a commercial IPCE measurement system (Beijing, Zolix, DSR 100UV-B). X-ray photoelectron spectroscopy (XPS) measurements were performed using Thermo ESCALAB 250 system.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 90,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All of the synthesis processes were carried out in the glovebox under Ar atmosphere. The Cs2AgSbxBi1\\u2212 xBr6 (x\\u202f=\\u202f0, 0.25, 0.50, 0.75) thin films were prepared by dip-coating from the DMSO solution containing 2\\u202fmmol CsBr (99.9%, Alfa Aesar) and 1\\u202fmmol AgBr (99.998%, Alfa Aesar), as well as x mmol (x\\u202f=\\u202f0, 0.25, 0.50, 0.75) SbBr3 (99.995%, Alfa Aesar) and (1\\u2212x) mmol BiBr3 (99%, Alfa Aesar). In a typical process, certain amount of CsBr, AgBr, SbBr3, and BiBr3 powdered precursors were put into a 10\\u202fmL glass bottle at the beginning. Then, a 2\\u202fmL 180\\u202f\\u00b0C preheated DMSO solution was added to trigger the dissolution. Following that, the precursors/DMSO mixture was kept on a hot plate at 180\\u202f\\u00b0C for around 10\\u202fmin until the complete dissolution of the precursors.\\nAfter the full dissolution of precursors, a frosted quartz slide substrate (with 5\\u202fcm in length and 1\\u202fcm in width) was dipped into the precursor solution (kept for around 5\\u202fs) and then slowly pulled out (with effective coating area around 1\\u202fcm2). The coated sample was heated immediately by suspending it above a hot plate (at 250\\u202f\\u00b0C and kept at around 5\\u202fmm away) and gently waggled with hands to ensure the steady and uniform evaporation of the DMSO solvent. After the full evaporation of the DMSO, the coated sample was then placed on the hot plate for annealing for around 0.5\\u202fh and wascooled down naturally to room temperature. Some of the prepared samples were annealed at 250\\u202f\\u00b0C for different times (i.e., 1, 2, 4\\u202fh) in order to further investigate their thermal stability.\\n\\nThe FTO-coated glass sheets were patterned through etching with Zn powder and 3\\u202fM HCl solution and subsequently cleaned with deionized water, acetone, isopropanol, and ethanol. The residual organic matter was further eliminated by plasma cleaner for 15\\u202fmin. Next, the dense TiO2 layer was prepared by spin-coating at 2000 r/min for 30\\u202fs using 70\\u202f\\u03bcL of tetraisopropyl titanate (C12H28O4Ti, 97%, Sigma\\u2013Aldrich) precursor solution, followed by annealing at 500\\u202f\\u00b0C for 30\\u202fmin upon the etched FTO glass. To prepare the aforementioned C12H28O4Ti precursor solution, the solution A (33\\u202f\\u03bcL of 2\\u202fM HCl added to 2.5\\u202fmL ethanol) was added to the solution B (350\\u202f\\u03bcL of C12H28O4Ti dissolved in 2.5\\u202fmL of ethanol) dropwise. Afterward, the mp-TiO2 layer was deposited on the dense TiO2 layer through spin-coating 80\\u202f\\u03bcL of the TiO2 nanoparticle paste (Dyesol-18NRT, Dyesol; dispersed in absolute ethanol with1:2 weight ratio) at 4500\\u202fr/min for 30\\u202fs, followed by annealing at 500\\u202f\\u00b0C for 30\\u202fmin.\\nThe double-perovskite Cs2AgSbxBi1\\u2212 xBr6 precursor solution was prepared under 180\\u202f\\u00b0C as mentioned above. Then, the precursor solution was spin-coated on the 180\\u202f\\u00b0C pre-heated FTO/dense TiO2/mp-TiO2 substrates at 3000 r/min for 30\\u202fs, followed by annealing under 250\\u202f\\u00b0C for 0.5\\u202fh under argon atmosphere. After the film formation and annealing, the double-perovskite photoabsorber layer was covered by the hole transport layer (HTL) through spin-coating at 3000\\u202fr/min for 30\\u202fs using 70\\u202f\\u03bcL 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobi-fluorene (spiro-MeOTAD) solution. The spiro-MeOTAD solution was prepared through dissolving 100\\u202fmg of spiro-MeOTAD, 40\\u202f\\u00b5L of 4-tert-butylpyridine (t-BP), 36.3\\u202f\\u03bcL of a 520\\u202fmg\\u202fmL\\u22121 Li-TFSI acetonitrile solution, and 60\\u202f\\u03bcL of a 300\\u202fmg\\u202fmL\\u22121 Co(III)-FK102-TFSI dopant acetonitrile solution in 1\\u202fmL chlorobenzene. Finally, around 600\\u202f\\u00c5 of Au was deposited onto the HTL layer by thermal evaporation.\\n\\nThe samples were characterized by a scanning electron microscope (MERLIN VP Compact, Carl Zeiss), X-ray diffraction (Smartlab, Rigaku; D8 ADVANCE, Bruker), transmittance spectroscopy (Cary 5000 UV\\u2013vis\\u202f\\u2212\\u202fNIR, Agilent Technologies).\\n\\nThe J\\u2013V curves of the double-perovskite solar cells were obtained by a Keithley 4200-SCS parameter analyzer sweeping from 1.5 to \\u22121 V at a scan rate of 10\\u202fmV\\u202fs\\u22121, illuminated under a solar simulator (AM 1.5G, 100\\u202fmW\\u202fcm\\u22122, 94043A, Newport). During the measurements, a 0.06-cm2 mask was used to confine the illuminated active area to avoid edge effects. The EQE spectrum of the Cs2AgSb0.25Bi0.75Br6 solar cell was measured by a quantum efficiency system (Oriel IQE-200, Newport).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: AgCs2BiBr6,\\n Perovskite_composition_short_form: AgCsBiBr,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 250,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK102; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials: N,N-dimethylformamide (DMF, 99.99%), chlorobenzene (CB, 99.9%), dimethyl sulfoxide (DMSO, 99.50%) and Isopropanol (IPA, 99.50%) were purchased from J&K (China). Toluene (99.7%) was purchased from Tian Hang Technology Co., Ltd.. Lead iodide (PbI2, 99.999%) and lead bromide (PbBr2, 99.9%) were purchased from TCI (Japan). Cesium iodide (CsI), formamidinium iodide (FAI), methylammonium bromide (MABr) were purchased from Dysol (Australia). Poly(bis(4-phenyl) (2,4,6-trimethylphenyl)amine) (PTAA), 2,3,5,6-Tetrafluoro-tetracyanoquinodimethane (F4-TCNQ), phenethylammonium iodide (PEAI), phenethylammonium bromide (PEABr), phenethylammonium chloride (PEACl), Methylammonium Chloride (MACl) and bathocuproine (BCP) were purchased from Xi'an Polymer Light Technology Corporation. Indene-C60 Busduct (ICBA) was purchased from ADS. All the commercial materials were used as received without re-purify. Silver was purchased from commercial sources with high purity.\\nDevice Fabrication of Perovskite Solar Cells: ITO glass substrates (15\\u00a0\\u03a9 sq\\u22121) were sequentially cleaned by sonication with detergent, deionized water, acetone, and isopropyl alcohol for 20\\u00a0min, respectively. Then, the ITO glass substrates were dried at 100\\u00a0\\u00b0C in oven. The cleaned ITO glass substrates were treated with oxygen plasma for 10\\u00a0min and then transferred into a N2-filled glovebox before use. The doped PTAA solution was prepared by adding 2\\u00a0wt% F4-TCNQ (1\\u00a0mg\\u00a0mL\\u22121 in CB) into PTAA solution (5\\u00a0mg\\u00a0mL\\u22121 in toluene) and stirring overnight. The as-prepared dope PTAA solution was spin-coated onto the ITO substrates at 4000\\u00a0rpm for 30\\u00a0s and the substrates were subsequently annealed at 150\\u00a0\\u00b0C for 10\\u00a0min. The perovskite precursor solution was prepared by mixing CsI, FAI, MABr, PbI2 and PbBr2 in DMF:DMSO (5:1/v:v) with a chemical formula of (FA0.6MA0.4)0.9Cs0\\u00b71Pb(I0\\u00b76Br0.4)3, and then 10\\u00a0mol% MACl was added into the perovskite precursor solution. The PTAA based substrates were pre-treated by spin-coating 50\\u00a0\\u03bcL of DMF at a speed of 5000\\u00a0rpm for 8\\u00a0s to improve the wettability of the PTAA before perovskite spin coating. The perovskite solutions were spin-coated onto glass/ITO/PTAA at 5000\\u00a0rpm for 30\\u00a0s 150\\u00a0\\u03bcL CB was slowly dripped onto the center of film at 12\\u00a0s before the end of spin-coating. The as-prepared perovskite films were subsequently annealed on hotplate at 65\\u00a0\\u00b0C for 5\\u00a0min and 100\\u00a0\\u00b0C for 15\\u00a0min. For the passivated devices, different concentrations (1.25, 2.5, 5\\u00a0mg\\u00a0mL\\u22121) phenethylammonium halide (PEAI, PEABr, PEACl) in IPA was quickly dripped into the as-prepared perovskite films at 5000\\u00a0rpm 30\\u00a0s, and then annealed at 100\\u00a0\\u00b0C for 5\\u00a0min. Then the films were washed with 50\\u00a0\\u03bcL IPA at 5000\\u00a0rpm for 30\\u00a0s. For doped ICBA solution, ICBA (15\\u00a0mg\\u00a0mL\\u22121) and MAI (10\\u00a0mg\\u00a0mL\\u22121) were respectively dissolved in dichlorobenzene and isopropanol alcohol and stirred at 80\\u00a0\\u00b0C for 2\\u00a0h, then mix the ICBA and MAI solution in a v/v % of 9:1, then the 25\\u00a0\\u03bcL mixed solution was spin-coated onto the top of perovskite films at 1500\\u00a0rpm for 25\\u00a0s, 6500\\u00a0rpm for 15\\u00a0s, following with the 70\\u00a0\\u00b0C for 5\\u00a0min annealing. The spin-coating processes were all conducted when the substrates and films were at room temperature. Finally, 20\\u00a0nm C60, 6\\u00a0nm BCP and 100\\u00a0nm silver electrode was thermally evaporated under high vacuum (<4\\u00a0\\u00d7\\u00a010\\u22126\\u00a0Torr). The device area was defined and characterized as 0.13\\u00a0cm2 by metal shadow mask.\\nCharacterization: J\\u2013V characteristics of photovoltaic devices were measured in N2-filled glovebox at room temperature by using a Keithley 2400 source meter under simulated AM 1.5G illumination with an intensity of 100\\u00a0mW\\u00a0cm\\u22122 from a solar simulator (Enlitech, SS-F5, Taiwan) and under indoor light sources (PAK-LED-T5-4WF-865 (3000\\u00a0K), PAK09481 (2700\\u00a0K)). A National Renewable Energy Laboratory calibrated silicon solar cell with a KG2 filter was used to calibrate the intensity of light from solar simulator. A high-precision fibre-optics spectrometer (OCEAN-HDX-XR, Ocean Optics) was employed to measure the spectra and illumination intensities of the indoor light sources. A shading mask with aperture area of 0.105\\u00a0cm2 was applied to cover the devices to ensure the accuracy of current density from J-V curves. J-V curves were measured in forward scan from \\u22120.2 to 1.3\\u00a0V, and in reverse scan from 1.3\\u00a0V to \\u22120.2\\u00a0V, along with a scan step of 20\\u00a0mV and a dwell time of 10\\u00a0ms. X-ray diffraction (XRD) characterization was carried out in a D2 Phaser instrument with a Cu K\\u03b1 (\\u03bb\\u00a0=\\u00a00.154\\u00a0nm) radiation. All photoemission studies were carried out in a VG ESCALAB 220i-XL surface analysis system equipped with a He-discharge lamp (hv\\u00a0=\\u00a021.22\\u00a0eV) for UPS investigation. The morphology of the samples was monitored by SEM (QUATTRO S). PL and TRPL results were recorded with a FLS980 spectrofluorometer (Edinburgh). The perovskite films for PL and TRPL measurements were deposited on quartz substrates. UV\\u2013Vis absorption spectra were measured with a UV\\u2013Vis spectrometer (PerkinElmer model Lambda 2S). EQE measurements were carried out by a QE-R EQE system (EnLi Technology, Taiwan). The thicknesses of films were measured by using a DektakXT Profiler (Bruker).\\n\", \"output\": \"<s> Substrate_stack_sequence: ,\\n ETL_stack_sequence: ICBA; C60; BCP,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: ,\\n Perovskite_composition_long_form: Cs0.1FA0.6MA0.4PbBr0.4I0.6,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: PEACl,\\n Perovskite_deposition_solvents: ,\\n Perovskite_deposition_procedure: ,\\n Perovskite_deposition_thermal_annealing_temperature: ,\\n Perovskite_deposition_thermal_annealing_time: ,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: ,\\n Backcontact_stack_sequence: ,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: ,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: ,\\n Stability_atmosphere: ,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: ,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: Unknown,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"180\\u202fnm of indium tin oxide (ITO) coated glass substrates with a sheet resistance of 8\\u202f\\u03a9/sq were purchased from Huayulianhe Co. Ltd. SnO2 colloid precursor (tin (IV) oxide, 15% in H2O colloidal dispersion), anhydrous dimethyl sulfoxide (DMSO), RbBr (99.8%) and chlorobenzene were obtained from Alfa Aesar. CsBr (99.9%) and spiro-OMeTAD were obtained from Xi'an Polymer Light Technology Corp (PLT). BiBr3 (98%), Lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI) and 4-tertbutylpyridine (tBP) were obtained from Aldrich. AgBr (99.99%) were purchased from Aladdin. All these commercially available materials were used as received without any further purification.\\n\\nThe precursor solution was prepared by mixing CsBr:RbBr (1\\u202fM) at 100:0, 95:5, 90:10 and 85:15 for (Cs1-xRbx)2AgBiBr6 with different x, AgBr (0.5\\u202fM) and BiBr3 (0.5\\u202fM) in DMSO at 70\\u202f\\u00b0C with stirring until fully dissolved.\\n\\nThe ITO glass was sequentially cleaned in deionized water, acetone, and ethanol under ultrasonic each for 30\\u202fmin, and then treated with oxygen plasma for 10\\u202fmin. The SnO2 electron transport layer was prepared by spin-coating dispersed SnO2 colloid in deionized water (volume ratio of 1:6) at a speed of 3000\\u202frpm, then annealed at 150\\u202f\\u00b0C for 30\\u202fmin. After filtered by 0.22\\u202f\\u03bcm pore sized filter, the (Cs1-xRbx)2AgBiBr6 precursor solution was spin-coated on the SnO2 film at 1000\\u202frpm for 10s and 2000\\u202frpm for 20\\u202fs respectively. After that, the film was quickly moved to low pressure equipment followed by pumping to 20\\u202fPa, then it was annealed at 250\\u202f\\u00b0C for 10\\u202fmin. When the substrate was cooled to room temperature, Spiro-OMeTAD (72.3\\u202fmg/mL) chlorobenzene solution, which was employed with the addition of 35\\u202f\\u03bcL of Li-TFSI/acetonitrile (260\\u202fmg/mL) and 29\\u202f\\u03bcL of tBP, was spin-coated on the perovskite layer at 4000\\u202frpm for 30\\u202fs to make the hole transport layer. Finally, Au electrode was deposited by thermal evaporation at a rate of 0.3\\u202fnm\\u202fs\\u22121 using a shadow mask to pattern the electrode. The active area of solar cell is 0.1\\u202fcm2. Except for thermal evaporation, the whole process is carried out under ambient condition with a relative humidity (RH) of \\u224835%.\\n\\nThe X-ray diffraction (XRD) patterns were measured using X-ray diffraction system (PANalytical Inc.) with monochromatic Cu K\\u03b1 irradiation (\\u03bb\\u202f=\\u202f1.5418\\u202f\\u00c5). UV\\u2013visible absorption spectrum was measured by using a UV\\u2013vis\\u2013NIR pectrophotometer (UV3600Plus). SEM images were recorded by using a highresolution scanning electron microscopy (Hitachi S-4800). The steady-state photoluminescence (PL), excited at 400\\u202fnm, was measured with NaonLog infrared fluorescence spectrometer (Nanolog L3-2Ihr). The time resolved photoluminescence (TRPL) measurement was measured using UltraFast Lifetime Spectrometer (Delta flex). Photovoltaic performances were measured by using a Keithley 2611 source meter at AM 1.5G illumination (100\\u202fmW\\u202fcm\\u22122) under a Newport Thermal Oriel 69911300\\u202fW solar simulator. The system was calibrated against a certified reference silicon solar cell. Effective area of each cell was 0.1\\u202fcm2 defined by masks for all the photovoltaic devices discussed in this work. The rate of current density\\u2013voltage (J-V) curves scan is 0.065\\u202fV\\u202fs\\u22121. The incident photon-to-current conversion efficiency (IPCE) spectrum was observed using a lock-in amplifier (model SR830 DSP) coupled with a 1/4\\u202fm monochromator (Crowntech M24-s) and 150\\u202fW tungsten lamp (Crowntech). All of the measurements of the solar cells were performed in an ambient atmosphere at room temperature without encapsulation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: AgCs2BiBr6,\\n Perovskite_composition_short_form: AgCsBiBr,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 250,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Stoichiometric formamidinium iodide and bismuth(III) iodide (BiI3) were dissolved in N,N-dimethylformide (DMF) and dimethyl sulfoxide (DMSO) at a Bi3+ concentration of 1.5\\u202fmmol/L and then filtered for further usage. Fluorine-doped SnO2 glass (FTO glass, 2.0\\u202f\\u00d7\\u202f2.0\\u202fcm2, Huanan Xiangcheng Tech.) was cleared by isopropanol, acetone, deionized water, and alcohol in an ultrasonic cleaner, dried, and then treated by ultraviolet ozone treatment before use. In accordance with the procedure described in a reference (Lan et al., 2017), the TiO2 precursor was spin-coated on the FTO glass and then sintered at 450\\u202f\\u00b0C for 30\\u202fmin to form a compact layer. Subsequently, TiO2 paste (30NR-D, Dyesol, Queanbeyan, Australia) diluted by alcohol (weight ratio of 1:6) was spin-coated on the dense TiO2 compact layer and then sintered at 500\\u202f\\u00b0C for 30\\u202fmin to form a mesoporous structure. After cooling down to 120\\u202f\\u00b0C, the substrates were immediately transferred into the N2 atmosphere glovebox for perovskite preparation. Bi-based perovskite precursors (40\\u202f\\u00b5L) were dropped on the mesoporous TiO2 layer, spin-coated at 1600\\u202frpm for 30\\u202fs, and then annealed at 120\\u202f\\u00b0C for 20\\u202fmin. FA-based bismuth perovskite films prepared from DMF and DMSO were labeled as \\u201cFA-Bi-DMF\\u201d and \\u201cFA-Bi-DMSO,\\u201d respectively. For comparison, MA-based bismuth perovskite (MA3Bi2I9) films were also prepared with the same method and labeled as \\u201cMA-Bi-DMF.\\u201d\\n\\nMesoporous-structural electron transport layers were chosen for device fabrication. In detail, TiO2 and perovskite layers were prepared as mentioned above. Subsequently, 72.3\\u202fmg of Spiro-OMeTAD in 1\\u202fmL of chloridebenze solution was used as hole transport materials with the addition of 28\\u202f\\u00b5L of 4-tert-butylpyridine and 19\\u202f\\u00b5L of TSFI-Li acetonitrile (520\\u202fmg/mL). It was spin coated on the bismuth perovskite films at 3000\\u202frpm for 30\\u202fs. Finally, 50\\u202fnm of Au film was deposited as the top electrode by thermal evaporation. The devices fabricated on the different perovskites were correspondingly labeled.\\n\\nThe phase structures of the films were analyzed using powder X-ray diffraction (XRD, Ultima IV, Rigaku, Tokyo, Japan) with CuK\\u03b1 radiation (\\u03bb\\u202f=\\u202f0.15406\\u202fnm) operated at 40\\u202fkV and 40\\u202fmA. The surface and cross-sectional morphologies of the prepared films were analyzed by field-emitted scanning electron microscopy (FE-SEM, SUPRA 55, Zeiss, Germany). The composition of the film was mapped by an energy dispersive X-ray microanalysis system (EDX, Bruker QUANTAX 200, Bruker, USA). Atomic force microscopy (AFM, Agilent 5420, USA) was applied to determine the surface distribution of the films. Photoluminescence (PL) was carried out using a time-resolved and steady-state spectroscope (FluoTime 300, PicoQuant GmbH) from 600 to 800\\u202fnm. UV\\u2013visible spectra were obtained on a spectrophotometer (UV-3600Plus, Shimadzu, Japan). Current density\\u2013voltage (J\\u2013V) characteristics of the perovskite solar cells were tested under simulated AM 1.5G conditions (100\\u202fmW/cm2) with a Keithley 2400 source meter under ambient conditions in-house. The voltage was scanned from 0 to 0.70\\u202fV with a scan rate of approximately 0.01\\u202fV/s. Device area illuminated was precisely set by a mask with an area of 0.1\\u202fcm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MA3Bi2I9,\\n Perovskite_composition_short_form: MABiI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The monomers 3-thiopheneacetic acid (TAA) and 3-hexylthiophene (HT) were purchased from Sigma-Aldrich. The TAA monomer (1) was esterified with methanol by refluxing with a catalytic amount of concentrated H2SO4 for 24 h to protect the carboxylic acid group during polymerization. The HT monomer and different mole fractions of the protected monomer 3-thiophene methyl acetate (3TMA, 2) were dissolved in chloroform and then added slowly to an oxidant solution of anhydrous ferric chloride in anhydrous chloroform under an N2 atmosphere at 0 \\u00b0C in a two-necked round-bottomed flask and kept under stirring for 24 h. The molar ratio of the oxidant and monomer was maintained at 4:1 in all cases. After the polymerization, a dark red copolymer, namely, P3TMA-co-P3HT (3), was precipitated by adding an excess amount of methanol. Oligomers and residual oxidant were removed by repeated washing of the precipitate with methanol and deionized water, respectively. A deprotection reaction was performed by heating P3TMA-co-P3HT (0.5 g) in 50 mL of a 2 M NaOH solution for 72 h, and it was then filtered to remove insoluble components. The water-soluble part (4) was neutralized by adding a dilute HCl solution. The resulting precipitate (P3TAA-co-P3HT, 5) was washed with deionized water, collected by centrifugation and dried in a vacuum. The whole procedure of synthesizing the copolymers with different compositions is presented in Scheme 1, and the component polymers were also synthesized via the same procedure for comparison purposes.\\nThe weight-average molecular weight (Mw) was measured by gel permeation chromatography (GPC) (Waters Instruments) equipped with an ultra-Styragel column with polystyrene as a standard using THF as the eluent at 40 \\u00b0C. 1H NMR spectra were used to determine the chemical structures of the copolymers and the mole percentages of the components in the copolymers. The 1H NMR spectra (Fig. S1(a\\u2013d), ESI\\u2020) were in agreement with the structures of the copolymers.\\n\\nZnO NPs were synthesized via a previously reported procedure.\\n\\nMAI was prepared using a method reported in the literature. Methylamine (40% in water, Spectrochem) was mixed with the dropwise addition of hydroiodic acid (HI, 57 wt%, Sigma-Aldrich) in a molar ratio of 1.2:1 at 0 \\u00b0C with stirring. After being stirred for 2.5 h, the solvent (water) was removed by a rotary evaporator at 60 \\u00b0C. Then, the product that was obtained was washed using diethyl ether and recrystallized from ethanol. The resulting white powder was dried at 60 \\u00b0C for 24 h in a vacuum and stored in a vacuum desiccator.\\n\\nFirstly, glass coated with fluorine-doped tin oxide (FTO) (sheet resistance of 8 \\u03a9 sq\\u22121, Dyesol) was etched by zinc dust and concentrated HCl. It was then cleaned in an ultrasonic bath using a soap solution, deionized water, acetone and isopropanol, each for 10 min, respectively. Then, a thin layer of ZnO nanoparticles was spin-coated onto the FTO substrate at 3000 rpm for 30 s. The procedure was repeated three times to obtain a continuous film. Next, 461 mg lead iodide (PbI2) and 159 mg MAI were dissolved in 1 mL \\u03b3-butyrolactone (GBL) at 70 \\u00b0C overnight. The MAPbI3 solution was spin-cast on the ZnO layer at 3000 rpm for 30 s. Later, the substrates were annealed at 100 \\u00b0C for 10 min. The polymeric HTM in a THF solution (10 mg mL\\u22121) was spin-coated on top of the perovskite film at 2500 rpm for 40 s. In addition, one reference device was fabricated using spiro-MeOTAD as the HTM and ZnO as the ETM. To prepare a spiro-MeOTAD solution, 80 mg spiro-MeOTAD, 28.5 \\u03bcL 4-tert-butylpyridine, and 17.5 \\u03bcL of a solution of lithium bis(trifluoromethanesulfonyl)imide (520 mg in 1 mL acetonitrile) were dissolved in 1 mL of chlorobenzene and coated on the perovskite film by spin-coating at 4000 rpm for 30 s. Finally, a cathode layer of 100 nm Ag was deposited on the polymeric HTM layer by thermal evaporation at an evaporation rate of 2.5 \\u00c5 s\\u22121 under vacuum conditions of 1 \\u00d7 10\\u22126 mbar. All steps of the device fabrication were carried out in ambient conditions.\\n\\nThe 1H NMR spectra of samples were recorded with a 500 MHz Bruker instrument using DMSO-d6 as a solvent. X-ray diffraction data were recorded using a Bruker AXS diffractometer (D8 Advance) with Cu K\\u03b1 radiation and fitted with a Lynx Eye detector. The data were recorded with a step size of 0.05\\u00b0 (2\\u03b8). The morphology and microstructural images were studied using a scanning electron microscope (Zeiss EVO MA 10). The FTIR spectra of the samples were recorded on a silicon wafer using a PerkinElmer Spectrum 100 instrument. UV-vis absorption spectra were recorded in the solid state on a quartz plate using a UV-vis spectrophotometer (Agilent Cary 8454). The PL spectra of the solid films on a quartz surface were recorded using a Fluoromax-3 instrument (Horiba Jobin Yvon). Time-resolved PL (TRPL) measurements of the MAPbI3 film with different HTMs were made with a time-correlated single-photon counting (TCSPC) system (Horiba Jobin Yvon IBH). Samples were photoexcited using a 440 nm laser beam. The lifetime was calculated by fitting the decay plot generated for the MAPbI3/HTM films with a biexponential decay function of the following form:\\nCyclic voltammetry experiments were carried out with an electrochemical workstation (CHI 6002E) consisting of a platinum wire counter electrode, platinum working electrode, and Ag/AgCl quasi-reference electrode in a three-electrode cell configuration with a ferrocene/ferrocenium (Fc/Fc+) internal standard at a scan rate of 50 mV s\\u22121. P3TAA-co-P3HT dissolved in THF was cast on the working electrode, which was followed by coating with Nafion. The measurements were carried out with 0.1 mol L\\u22121 tetrabutylammonium hexafluorophosphate (TBAPF6) as the background electrolyte in dry acetonitrile. All solutions were degassed with ultrapure nitrogen, and throughout the experiment a nitrogen atmosphere was maintained.\\n\\nThe J\\u2013V characteristics of the PSCs were studied in ambient conditions using a Keithley 2401 source measurement unit. The cells were illuminated by a 150 W solar simulator equipped with an AM 1.5G filter (Oriel Instruments, Newport) at a calibrated intensity of 100 mW cm\\u22122. The effective cell area was limited to 0.32 cm2 using a non-reflective mask. IPCE measurements were carried out with a Newport 67005 150 W Xe lamp in combination with an Oriel Cornerstone 130 monochromator and a Keithley 236 source measurement unit operated by Visual Basic software. EIS measurements were performed using a Solartron SI1260 impedance/gain-phase analyzer in the frequency range from 1 MHz to 0.1 Hz under an open-circuit DC bias and at a voltage perturbation of 10 mV. All the device formation and characterization was carried out under ambient conditions (temperature 30 \\u00b0C, humidity 70\\u201380%).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.32,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide was purchased from Dyesol, PbI2 (99.999%), PbCl2 (99.999%), tetrahydrothiophene-1-oxide (THTO) (96%), gamma-butyrolactone (gBL) 99%, dimethylformamide (DMF) anhydrous, 99.8%, titanium diisopropoxide bis(acetylacetonate) 75% wt in isopropanol, isopropanol (IPA) (99%), methanol (99%), nickel acetate tetrahydrate (99%), and diethanolamine (98%) were purchased from Sigma Aldrich and used as received. Dimethylsulfoxide (DMSO) 99.9% was purchased from VWR International. PEDOT:PSS (Clevios HTL solar #1) was purchased from Heraeus and filtered with a 0.45 \\u03bcm pore size PVDF filter before use. PCBM was purchased from nano-C. ITO substrates (15 ohm cm\\u22122) were purchased from Kintec. Aluminum evaporation material (99.999%) was purchased from Kurt J Lesker company.\\n\\n1 to 1 molar ratio of MAI and PbI2 were dissolved in gBL at 70 \\u00b0C with THTO additive at a molar ratio of three THTO to one Pb (3:1 THTO:Pb). The solution was 30% MAPbI3 by weight. This solution was cooled to room temperature and spin-coated on various substrates such as ITO/PEDOT:PSS, ITO, TiO2, NiO and SiO2 at 2000 rpm for 30 seconds. After spin-coating the precursor solution, the samples were annealed at 70 \\u00b0C for 30 minutes to obtain MAPbI3 thin films.\\n\\nPEDOT:PSS was spin-coated at 1500 rpm for 40 seconds and annealed at 170 \\u00b0C for 4 minutes. For NiOx, a 0.4 mol L\\u22121 solution of nickel acetate and diethanolamine in methanol was used. This solution was spin-coated at 3000 rpm for 30 seconds and annealed at 400 \\u00b0C for 10 minutes. For TiO2, titanium diisopropoxide bis(acetylacetonate) in IPA as purchased from Sigma Aldrich was diluted further with IPA until the concentration was 0.3 mol L\\u22121. This solution was spin-coated at 3000 rpm for 30 seconds and annealed at 400 \\u00b0C for 10 minutes.\\n\\nFilms were spin-coated on a glass/PEDOT substrate at 2000 rpm for 30 seconds from a precursor solution consisting of 0.8 M PbCl2 and 2.4 M MAI in DMF. The films were annealed at 120 \\u00b0C for 10 minutes in ambient conditions (relative humidity = 30%).\\n\\nA PANalytical X'Pert X-ray diffraction system with a Cu source operating at 40 kV and 40 mA was used. All measurements were performed ex situ at room temperature.\\n\\nData were taken at the D-1 beamline at the Cornell High Energy Synchrotron Source using X-rays with a wavelength of 0.1168 \\u00c5, a custom precision goniometer, and a Pilatus 200k two dimensional pixel array detector (Dectris). Samples were spin-coated at the beamline (Chemat), using the same protocol as for the ex situ XRD measurements. The temperature of the custom-built sample holder was controlled by a temperature controller (Digi-Sense) and the temperature was monitored during X-ray data collection. The X-ray beam was approximately 0.5 mm wide and 0.1 mm high, and illuminated the entire length (5 mm) of the sample using an incident angle of typically 0.5\\u00b0. For obtaining depth profiles, the incident angle was varied between 0.1\\u00b0 and 0.5\\u00b0. For all in situ data collection, the sample was moved to a new position after three GIXD patterns were collected, in order to avoid beam damage.\\n\\n1 inch by 1 inch patterned ITO substrates were cleaned by sonication with Hellmanex 3 surfactant in deionized water, pure deionized water, then ethanol, and UV-ozone cleaned for 5 minutes. PEDOT:PSS was spin-coated at 1500 rpm for 40 seconds and annealed at 170 \\u00b0C for 4 minutes. MAPbI3 thin film with preferential crystallographic orientation was deposited from THTO added solution as described previously. A 2% weight solution of PCBM was spin-coated at 1000 rpm. The metal contacts were deposited by evaporating 50 nm of aluminum at a rate of 0.1 nm s\\u22121 in a vacuum of 10\\u22126 Torr. Devices utilizing the same exact architecture were fabricated with a randomly oriented MAPbI3 thin film by using the interdiffusion method. Briefly, 1 M PbI2 in DMF was spin-coated at 3000 rpm, followed by 50 mg mL\\u22121 MAI in IPA. The film was annealed at 85 \\u00b0C for 1 hour.\\n\\nThe devices were tested with a Keithley source-meter using a scan rate of 1 V s\\u22121 under AM 1.5 illumination from a solar simulator (PV Measurements). The light source was calibrated with a reference silicon solar cell (PV Measurements). The device active area was 0.03 cm2. An optical mask was used to block illuminating the non-device area during testing.\\n\\nSEM images were taken with a Quanta 650 SEM operating at 30 kV. All samples were imaged at four or more locations and pictures presented in this work are representative of typical results near the center of the sample. Samples were prepared in the same manner as for solar cells without the PCBM and Al layers on top of the MAPbI3 layer.\\n\\nThe MBO value for atom\\u2013atom interactions in a (non-periodic) solvent-lead cluster were calculated using an ab initio approach, optimized with the B97-D3 functional and the PWPB95 functional using the Orca DFT package. Electronic structures of the optimized gas phase molecule were used to calculate the MBO of individual atomic interactions between oxygen and the central atom and, subsequently, the \\u201cbond unsaturation\\u201d value. The bond unsaturation is defined as the formal bond order (two in the case of oxygen) minus the Mayer bond order. Bond unsaturation, rather than the MBO itself is the key quantity, it provides a measure of the driving force for bonding (see the ESI\\u2020 for more details).\\n\\n20 configurations were generated for the coordinated Pb2+ molecule clusters and pure solvent molecule clusters using Packmol, each with a different random seed. Adequate sampling is necessary for the variety of configurations that complexes may assume. Subsequently, the systems were subjected to molecular dynamics minimizations, performed in LAMMPS using OPLS 2005 parameters. The non-periodic DFT code, Orca was used for further geometry optimizations and energy calculations. These optimizations eliminated the congestion on the Pb2+ ion that resulted from the necessity to use a Ba2+ ion (the closest in size to lead) during the MD annealing process, since Pb2+ parameters are not yet available in the OPLS force field. Using these relaxed geometries as starting configurations, further geometry optimization using B97-D3 ( )/def2-TZVP obtained more accurate structures and energies. The enthalpy of solvation was then calculated from the energies of the resulting geometries (see the ESI\\u2020 for more details).\\n\\nDFT calculations for periodic systems were performed using the Vienna Ab Initio Simulation Package (VASP) package employing a Perdew\\u2013Burke\\u2013Ernzerhof (PBE) density functional. The ion\\u2013electron interactions were described by the projector-augmented wave method using soft potentials. We relaxed all atoms in the system such that the forces were less than 0.01 eV \\u00c5\\u22121, and the self-consistent field was terminated when the energy is converged to less than 10\\u22126 eV. The electronic wavefunction was expanded using plane waves with an energy cutoff of 280 eV. We used a supercell approach to model the different slabs with 20 \\u00c5 of vacuum to mitigate interactions between fictitious images along the non-periodic direction of the slab. The cubic phase was modeled using 2 \\u00d7 1 surface supercell, while the tetragonal phase was modeled using 2 \\u00d7 2 surface supercell. The Brillouin zone was sampled using a 2 \\u00d7 2 \\u00d7 1 (2 \\u00d7 3 \\u00d7 1) k-grid for the tetragonal (cubic) surfaces, and 2 \\u00d7 2 \\u00d7 2 (3 \\u00d7 3 \\u00d7 3) for the tetragonal (cubic) bulk phases. The THTO molecule was adsorbed on the top and bottom sides of the slab to minimize the dipole of the system along the non-periodic direction. Other computational details are reported in the ESI.\\u2020\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 85.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 60.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.03,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"We used patterned indium-doped tin oxide (ITO) coated glass substrates (15 \\u03a9 cm\\u22122), lead iodide (PbI2, Sigma Aldrich, 99.9%), lead bromide (PbBr2, Sigma Aldrich, 99.99%), [6,6]-phenyl-C61-butyric acid methyl ester (PCBM, Solenne BV), PEDOT:PSS (Clevios F HC Solar, SCA 418-12), nickel chloride hexahydrate (NiCl2\\u00b76H2O, Sigma Aldrich, 99.9%), cesium iodide (CsI, Sigma Aldrich, 99.99%), and sodium hydroxide (NaOH, Sigma Aldrich, \\u226598%). Methyl ammonium bromide (MABr), methyl ammonium iodide (MAI) and formamidinium iodide (FAI) were synthesized in our lab, as mentioned in the synthesis of organic halides. Titanium(IV) isopropoxide (Ti[OCH(CH3)2]4, Sigma Aldrich, 99.9+%), isopropanol, hydroiodic acid (HI, 57 wt% in H2O), hydrobromic acid (HI, 57 wt% in H2O), methylamine (CH3NH2, Aldrich, 33 wt% in absolute ethanol), aluminum, N,N-dimethylformamide (DMF, anhydrous, Sigma Aldrich), dimethylsulfoxide (DMSO, Anal. R. VWR chemicals, 99.5%), acetone, ethanol, Helmanex\\u00ae detergent, chlorobenzene, 2-methoxyethanol (CH3OCH2CH2OH, Sigma Aldrich, 99.9%) and ethanolamine (H2NCH2CH2OH, Sigma Aldrich, 99%) were also used.\\n\\nFirst, indium doped tin oxide (ITO) substrates were ultrasonically cleaned in acetone, detergent, deionized water and IPA, sequentially. The hole transporting layer (HTL), NiOx, was deposited at 4000 rpm for 30 s and annealed at 140 \\u00b0C for 20 min. PEDOT:PSS (Clevios F HC) was spin-coated at 2500 rpm for 45 s and dried at 120 \\u00b0C for 15 min, followed by IPA washing via spin-coating at 4000 rpm for 15 s and heating at 120 \\u00b0C for 15 min. Then, HTL coated substrates were transferred into a glove box to deposit the perovskite film.\\nMixed-cation\\u2013mixed-halide perovskite (Cs0.05(FA0.83MA0.17)0.95PbI3\\u2212xBrx) solution was prepared by mixing PbI2 (507.5 mg), FAI (172 mg), MABr (22.4 mg) and PbBr2 (73.5 mg) in 1 mL of dry N,N-dimethylformamide and dimethylsulfoxide solvent mixtures (with 4:1 (v/v) ratio), followed by stirring at 45 \\u00b0C. Then, approximately 0.063 mol of CsI from 1.5 M stock solution (in DMSO) was added to the mixture and stirred overnight. The perovskite (PVS) solution was deposited on top of the HTL by a two-step spin-coating at 1500 rpm for 10 s with ramp 9 and at 6000 rpm for 30 s with ramp 2. During the second step, anti-solvent quenching was conducted via adding about 200 \\u03bcL of chlorobenzene starting at the 23rd s for about 3 s. Then, the film was annealed at 100 \\u00b0C for 60 s. After the films had cooled, 2% (wt/wt) of PCBM in a mixture of chlorobenzene and chloroform (50:50 volume ratio) was spin-coated on top of the PVS film. Diluted TiOx sol\\u2013gel solution was spin-coated on top of PCBM at 4000 rpm for 30 s, followed by annealing at 110 \\u00b0C for about 5 min in ambient air. Finally, the inverted PSC fabrication was completed by thermal evaporation of 110 nm Al back electrode, which gave the PCBM/TiOx/Al sample and PCBM/Al control devices.\\n\\nSurface morphologies of films were characterized by atomic force microscopy (AFM, Bruker Innova) and scanning electron microscopy (SEM, ZEISS 1540 XB cross-beam scanning microscope with a focused ion-beam (FIB) unit). Crystal structure, phase, and chemical information of the perovskite film were investigated by X-ray diffraction (Bruker D8 XRD system) employing Cu and K\\u03b1 radiation source (\\u03bb = 1.5418 nm at 40 kV and 20 mA). Characteristic photocurrent density\\u2013photo voltage (J\\u2013V) response of the cells was recorded with a Keithley-2400-LV source meter with LabVIEW software. A LOT-QD solar simulator with 150 W xenon lamp emitting AM1.5 global spectrum and 100 mW cm\\u22122 light intensity, which was calibrated using a standard Si reference diode, was used for irradiation. External-quantum efficiency (EQE) was measured using an optical setup consisting of a lock-in amplifier (SR830, Stanford Research Systems) and a Jaissle 1002 potentiostat functioning as a preamplifier. The devices were illuminated with light from a xenon lamp passing through a monochromator (Oriel Cornerstone). A filter wheel holding long-pass filters and a mechanical chopper was mounted between the xenon lamp and the monochromator. Chopping frequencies in the range of 10\\u2013200 Hz were used. A calibrated silicon diode (Hamamatsu S2281) was used as a reference for light intensity at each wavelength. A halogen lamp (Philips 50 W, 12 V) was used to provide a variable white light bias to the solar cells while EQE was measured.\\nElectrochemical impedance spectroscopy characterization was conducted under light perturbation in the frequency range of 1 MHz to 0.01 Hz using a Solaron potentiostat coupled with THORLABS DC2100 LED driver equipped with a detector (M590L3) and XM PhotoEchem software. Optical characterization was performed by recording photoluminescence decay, electroluminescence (EL) and photoluminescence (PL) measurements. To measure PL, the samples were excited with a VIOFLAME 405 nm laser (COHERENT UV GaN-based, 25 mW) and the signal was recorded with a Shamrock SR-303i monochromator and Andor\\u2122 iDus Si-CCD detector. EL characterization was performed using a Shamrock SR-303i monochromator and an Andor\\u2122 iDus Si-CCD detector to measure the signal and Keithley-2400-LV source meter to measure current under different voltage bias. Photoluminescence decay measurement was conducted using Shamrock (SR-303i\\u2013A) monochromator equipped with an intensified charge-coupled device camera [Andor iStar DH320T-18U-73 (gate step, 2.5 ns; gate width, 2.5 ns)] and Nd:YAG laser (Spit light Compact 100) emitting at 532 nm with a pulse length of \\u223c10 ns.\\n\\nTo test the relative stability of PSCs, maximum power point tracking of encapsulated solar cells was performed in ambient air as well as in a glove box with oxygen level in the range of 0.1\\u201310 ppm under AM1.5 global spectrum illumination with continuous ventilation to keep the temperature low. J\\u2013V response of the devices was measured before and after maximum power point tracking. A white LED (XLamp CXA2011 1300K CCT) for ambient measurements and a 150 W xenon lamp for glove box measurements were used.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.17PbBr0.5I2.5,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PEDOT:PSS (Levios P VP. AL 4083) was obtained from Heraeus-(Precious Metals GmbH & Co. KG) Inc. Fullerene (99.5%); CH3NH3I (99.5%), bathocuproine (BCP) (98.0%) and PbI2 (99.999%) were obtained from Alfa Aesar. Dimethyl sulfoxide (DMSO) (\\u226599.0%); 4-hydroxybutanoic acid lactone (GBL) (\\u226599.0%) and toluene (\\u226599.0%) were purchased from Sinopharm Chemical. Reagent. Co., Ltd. Absolute ethanol (99.7%) and acetone (99.5%) were obtained from Nanjing chemical reagent co., Ltd.\\n\\nThe structure of the devices in this study is illustrated in Fig. 1. ITO glass substrates were cleaned in detergent, deionized (DI) water, acetone, and ethanol for 15 min in ultrasonicator (Shumei KQ300DE). After being dried with nitrogen gas, the ITO surface was treated with UV\\u2013ozone for 15 min. Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) layer was spin-coated on ITO at 3500 rpm for 1 min, followed by baking at 120 \\u00b0C for 60 min in air, and then the PEDOT:PSS-coated substrates were transferred into a glove box filled with high-purity N2. The 1.0 M CH3NH3I (MAI) and 1.0 M PbI2 for MAPbI3 solution were stirred in a mixture of GBL and DMSO (7:3 v/v) at 60 \\u00b0C for 12 h. The resulting solution was coated onto the PEDOT:PSS substrates by a one-step spin-coating process. During the spin-coating step, the substrate (around 1.5 cm \\u00d7 1.5 cm) was treated with toluene drop-casting. A detailed time-rotation profile for the spin-coating is shown in ESI Fig. S1.\\u2020 The film becomes darker after annealing at 100 \\u00b0C for 5 min. The C60 (30 nm), BCP (10 nm) and Al (120 nm) were thermally deposited on the substrate inside a vacuum chamber. The evaporation rates were monitored by a quartz oscillator system, and the film thickness was calibrated by a surface profiler (Veeco Dektak 6M). Finally, the devices with an active area of 0.11 cm2 were strictly encapsulated with UV-curable epoxy before being taken out from the glove box.\\n\\nThe current density\\u2013voltage (J\\u2013V) curves of the solar cells were measured with a computer-programmed Keithley 2400 source/meter under 100 mW cm\\u22122 illumination of simulated AM 1.5G sunlight (Newport's Oriel class A), which was calibrated by the JIS C 8912 standard. The incident photon to electron conversion efficiency IPCE spectra were measured by QTest Station 500AD Solar Cell Quantum Efficiency System (CROWNTECH, INC). The morphology of CH3NH3PbI films was measured by using scan electron microscope (SEM) (Hitachi S-4800). UV-Vis spectra were taken using a lambda 35 PerkinElmer ultraviolet-visible (UV-Vis) spectrophotometer. The crystallographic properties of CH3NH3PbI3 perovskite on the glass/PEDOT:PSS substrate were characterized by X-ray diffraction (XRD) with data recorded in the 2\\u03b8 range of 10\\u201350\\u00b0 at a step of 0.02\\u00b0. All measurements were carried out at room temperature. Time-resolved photoluminescent (PL) decay were measured using a FLS920 fluorescence spectroscopy (probed wavelength 550 nm, excitation wavelength 700 nm).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Anhydrous N,N-dimethylformamide (DMF, J&K Chemistry, 99.99%), anhydrous chlorobenzene (CB, Sigma-Aldrich, 99.9%), methylamine (CH3NH2, TCI, 33 wt% in MeOH), hydroiodic acid (HI, J&K Chemistry, 57 wt% in H2O), anhydrous 2-propanol (IPA, J&K Chemistry, 99.99%), titanium isopropoxide (Sigma-Aldrich, 99.999%), absolute methanol (J&K Chemistry, 99.99%), absolute acetone (J&K Chemistry, 99.99%), absolute diethyl ether (IPA, J&K Chemistry, 99.99%), PbI2 (Xi'an Polymer Light Technology Corp., 99.999%), phenylboronic acid (Sigma-Aldrich, 99.9%), Pd(0)(PPh3)4 (Sigma-Aldrich, 99.9%), K2CO3 (Sinopharm Chemical Reagent Co. Ltd., 99.9%), 2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9-(undecan-5-yl)-9H-carbazole and 3,6-dibromo-9-(4-bromophenyl)-9H-carbazole were purchased from commercial suppliers and used as received. Toluene (Sinopharm Chemical Reagent Co. Ltd., 99.99%) and THF (Sinopharm Chemical Reagent Co. Ltd., 99.99%) were stored over sodium wire (Sinopharm Chemical Reagent Co. Ltd., 99.99%) and freshly distilled from sodium benzophenone ketyl prior to use; linear polycarbazole (poly[N-(1-octylnonyl)-9H-carbazole-2,7-diyl], PCz) was purchased from Xi'an Polymer Light Technology Corp.; poly-3-hexylthiophene polymer (P3HT) was purchased from Aldrich Chemical, and used without further processing.\\n\\nHyper-branched polymer HB-Cz was synthesized from carbazole monomers and phenylboronic acid. The catalyst Pd(0)(PPh3)4 (0.023 g, 0.02 mmol), base K2CO3 (0.83 g, 6.0 mmol), monomers 3,6-dibromo-9-(4-bromophenyl)-9H-carbazole (1, 0.096 g, 2.0 mmol) and 2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9-(undecan-5-yl)-9H-carbazole (2, 0.172 g, 3.0 mmol) were added to the Schlenk tube equipped with a stirring bar in air. The Schlenk tube was fitted with a rubber septum, evacuated, and then refilled three times with nitrogen. Toluene (10.0 mL) was added via a syringe, and then the mixture was stirred for 1.5 h at 110 \\u00b0C. When the reaction solution became opaque, the end-capped phenylboronic acid was added and then stirred at 110 \\u00b0C for another 48 h. Excess absolute methanol was poured into the mixture, which was then filtered. The solid obtained was dissolved again in absolute THF, and the insoluble solid was filtered out. After removal of all the solvent, the solid residue was purified again by several precipitations from absolute THF into methanol; hydrazine hydrate (10%) was used for removal of trace Pd metal and the obtained solid residue was washed with excess acetone and next with methanol. In the end, the resultant HB-Cz polymer was obtained as gray powder with an yield of 85% (after purification), Mw = 6.4 \\u00d7 103, PDI = 2.12 (GPC, polystyrene calibration). 1H NMR (400 MHz, CDCl3) of HB-Cz: \\u03b4 (ppm) 0.81\\u20130.83 (\\u2013CH3), 1.19\\u20131.34 (\\u2013CH2\\u2013), 1.58 (\\u2013CH2), 2.08 (\\u2013CH2), 4.80 (\\u2013N\\u2013CH\\u2013), 7.30\\u20137.81 (Ar-H), 8.21\\u20138.61 (Ar-H). 13C NMR (400 MHz, CDCl3): \\u03b4 (ppm) 14.05, 22.61, 26.95, 29.25, 29.40, 29.53, 31.79, 33.90, 56.46, 107.64, 110.23, 127.03, 127.11, 127.30, 127.38, 127.86, 128.82, 129.01, 129.94, 134.90, 136.59, 137.77, 139.89, 140.31, 140.80, 141.44, 142.56, 143.28. Thermal properties of HB-Cz were tested via thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC).\\n\\nCH3NH3I (MAI) was synthesized according to the reported method. 10.0 mL of methylamine (40% in water) was added into 11.0 mL of hydroiodic acid (57 wt% in water) for 2 h with stirring under air and maintained in an ice-water bath. Afterwards the mixture obtained was evaporated at 50 \\u00b0C for around 2 h and white powder formed during this process. This was then washed with absolute diethyl ether three times and the as-obtained solid was re-dissolved in 10.0 mL absolute ethanol and precipitated with the addition of 125.0 mL absolute diethyl ether; this procedure was repeated three times. The white powder was collected and dried at 60 \\u00b0C in a vacuum oven for 24 h.\\n\\nThe PVSCs were fabricated with a structure of ITO/TiO2/MAPbI3/HTM/Ag. The patterned indium tin oxide (ITO) glass (sheet resistance = 15 \\u03a9 \\u25a1\\u22121) was pre-cleaned in an ultrasonic bath with deionized water, acetone and IPA, and finally treated in an ultraviolet-ozone chamber for 10 min. First, TiO2 precursor was spin-coated on top of ITO glass at 7000 rpm for 30 s in the glove box, and then baked at 130 \\u00b0C for 1 h in air. The resulting TiO2 films was treated in an ultraviolet-ozone chamber for 3 min and then transferred to the glove box. PbI2 was dissolved in dry DMF with a concentration of 463 mg mL\\u22121, and MAI was dissolved in anhydrous IPA at 10 mg mL\\u22121. MAPbI3 active layer was prepared through a modified solvent annealing two-step method developed by us. PbI2 precursors were spun onto compact TiO2-covered ITO glass at 3000 rpm for 30 s and dried at 40 \\u00b0C for 10 min; furthermore, MAI was spin-coated on top of the PbI2 layer at 3000 rpm for 30 s after 120 s loading time. MAPbI3 perovskite layers were thermally annealed on the heating panel at 90 \\u00b0C for 30 min to form and crystallize the MAPbI3 active layer. Then, HB-Cz, P3HT or PCz was deposited by spin-coating a 10\\u201320 mg mL\\u22121 CB solution at 1000 to 3000 rpm for 30 s and the obtained films were annealed at 90 \\u00b0C for another 5 min. Finally, the devices were transferred to a vacuum chamber and finished by evaporation of an 80 nm Ag electrode through a shadow mask. The devices were encapsulated in glass by UV-curable resin in the glove box, and measurements were taken in air.\\n\\n1H and 13C NMR spectra data were recorded on a Bruker AVIII-400 NMR spectrometer at room temperature and were expressed in parts per million (ppm) relative to the internal standard. Molecular weight and polydispersity of the polymer were determined by gel permeation chromatography (GPC) analysis with polystyrene standard calibration (Waters high pressure GPC assembly model 1515 pump, refractive index detectors, eluent solvent THF). UV-Vis absorption spectra of the films were obtained on a Shimadzu UV-2600 spectrometer. Thermogravimetric analysis (TGA) was recorded on a Mettler-Toledo TGA/SDTA 851e thermal apparatus (Switzerland) and differential scanning calorimetry (DSC) was run on a TA Instrument Q20 with scan rate of 10 \\u00b0C min\\u22121 under N2. Electrochemical impedance spectroscopy (EIS) was measured by a CHI 660 electrochemical workstation (CH Instruments Inc.) in the frequency range between 1 and 106 Hz with perturbation amplitudes of 10, 100, 200, 300, 400, 500, 600, and 700 mV. Cyclic voltammetry (CV) measurements were conducted using a three-electrode cell under N2 atmosphere with CHI 660 electrochemical workstation. The polymer films on a glassy carbon electrode (working electrode) were scanned anodically and cathodically in 0.1 M n-Bu4NPF6 in dry acetonitrile solution with Ag/AgCl and a Pt-wire as the reference and counter electrodes, respectively. The tests were calibrated with the standard ferrocene/ferrocenium (Fc/Fc+) redox system with the assumption that the energy level of Fc/Fc+ is 4.8 eV under vacuum. The crystal phase of the samples was examined by X-ray diffraction (XRD) (Bruker, D8-Advance X-ray diffractometer with Cu-K\\u03b1 radiation, \\u03bb = 1.54056 \\u00c5, 40 kV, 40 mA) from 2\\u03b8 = 5\\u00b0 to 60\\u00b0 at a scan rate of 0.02\\u00b0 s\\u22121 at room temperature under ambient conditions. The steady state photoluminescence (PL) spectrum was obtained via Perkin Elmer photoluminescence. The fluorescence decay traces were measured using a time-resolved fluorescence spectrometer (FLS980, Edinburgh) excited with a 397 nm EPL picosecond pulsed diode laser with a pulse width of 50 ps at room temperature in air. Scanning electron microscopy (SEM, JEOL JSM-6700F) and atomic force microscopy (AFM, Bruker Dimension Edge SPM System) were performed to characterize the surface morphology of different films.\\nSolar-simulated AM 1.5 sunlight was generated with a NEWPORT Sol3A class solar simulator (Newport Corp., Irvine, CA USA) calibrated to give 100 mW cm\\u22122 using a NREL-calibrated KG5-filtered silicon reference cell. The spectral mismatch factor was calculated to be less than 1%. The current density\\u2013voltage (J\\u2013V) curves were recorded with a Keithley 2400. The active areas of the solar cells were defined with a metal aperture mask of about 0.04 cm2. The external quantum efficiency (EQE) spectra of the solar cells were measured (Enlitech QE-R3011, Enlitech Co. Ltd., Taiwan) at room temperature.\\nHole mobility of the different HTMs was measured using the space-charge-limited current (SCLC) method. Hole-only devices were fabricated with a device structure of ITO/PEDOT:PSS/HTL/MoO3/Ag. The values of hole mobility were extracted by modeling the dark current under forward bias using the SCLC expression described by the Mott\\u2013Gurney law.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 90,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 30.0,\\n HTL_stack_sequence: HB-Cz,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Indium tin oxide (ITO)-coated glass substrates (2.5 \\u00d7 2.5 cm2, 20 \\u03a9 sq\\u22121) were cleaned with acetone, ethanol, and 2-propanol by ultrasonication in succession. Before their use, the ITO substrates were exposed to UV-Ozone (UVO) for 20 min. The (3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS, Clevios, P VP AI 4083) used in this study, diluted with methanol, was spin-coated onto the UVO-treated ITO substrate at 4000 rpm for 60 s and subsequently annealed at 150 \\u00b0C for 20 min in a N2-filled glove box. Methylammonium (MA) lead iodide, MAPbI3, perovskite film was grown via an anti-solvent engineering approach. A precursor solution was prepared by dissolving MAI and PbI2 (1.04:1 molar ratio) in a mixture of \\u03b3-butyrolactone (GBL) and dimethyl sulfoxide (DMSO) with a final concentration of 44 wt%. The precursor solution was spun onto the PEDOT:PSS layer at 1000 rpm for 10 s and 4500 rpm for 20 s in sequence. An appropriate amount of chlorobenzene was quickly dropped onto the film surface before the end of the second spin-coating step. The as-coated films were then annealed on a hot plate preheated to 100 \\u00b0C for 13 min. After cooling to room temperature, the 3\\u2032H-cyclopropa[1,9][5,6]fullerene-C60-Ih-3\\u2032-butanoic acid 3\\u2032-phenyl methyl ester (C60 PCBM, nano-C-PCBM-BF) solution at a concentration of 20 mg ml\\u22121 in chlorobenzene was spin-coated onto the MAPbI3 film at 2000 rpm for 60 s. The ZnO-NP solution (2.5 wt% in 2-propanol, Nanograde N10) was then spin-coated onto PCBM to form a buffer layer at 2000 rpm for 60 s. To fabricate semi-transparent devices, a 250 nm-thick Al-doped ZnO (AZO) transparent conducting layer was deposited onto the ZnO-NP layer via radio-frequency magnetron sputtering. The front-contact Ag grids were finally deposited by thermal evaporation for measurement in a substrate configuration (illumination from the opposite side of the substrate). The active area of the semi-transparent cells was about 0.4\\u20130.5 cm2, as defined by mechanical scribing. For the opaque devices, a 150 nm-thick Ag electrode as a charge collector was deposited onto the ZnO-NP layer by thermal evaporation through a shadow mask with an aperture size of 0.5 cm2. The active area of the opaque cells, which was defined by the overlapping area of the ITO and Ag electrodes, was 0.22 cm2.\\n\\nThe CISe devices were fabricated with the architecture of SLG/Mo/CISe/CdS/i-ZnO/AZO/Ni/Al. First, CISe thin films were deposited onto Mo-coated soda-lime glass (SLG) substrates by one-step electrodeposition in a 5.2 mM selenite-based electrolyte using a three-electrode system. Details of the procedure used to fabricate the electrodeposition are described in our previous paper. The as-prepared electrodeposited CISe films were thermally annealed at 580 \\u00b0C for 30 min in a Se vapor atmosphere to improve the crystallinity and microstructure of the films. The annealed films were then chemically etched in a 0.1 M KCN solution for 60 s to remove any CuxSe secondary phases. Subsequently, an n-type CdS buffer layer was deposited via chemical bath deposition for ca. 10 min at 60 \\u00b0C in a solution containing 2 mM CdSO4, 1.02 M NH4OH, and 84 mM thiourea to form 60 nm-thick layers. The intrinsic ZnO (i-ZnO) and AZO layers were sequentially deposited using radio-frequency magnetron sputtering. The device was then finalized by thermal deposition of the Ni/Al grids.\\n\\nTo fabricate the monolithic CISe/perovskite tandem devices, the CISe bottom cell and semi-transparent perovskite top cell were combined by having them share the i-ZnO/AZO layers in such a way that the perovskite cell was directly fabricated onto the AZO layer of the CISe solar cell. To avoid thermal degradation of the CISe/CdS junction properties, thermal annealing of the PEDOT:PSS layer was carried out at a comparatively low temperature of 120 \\u00b0C for 5 min. The remaining steps of the fabrication procedure were identical to those of the single-junction semi-transparent perovskite cell.\\n\\nThe cross-sectional morphologies of the perovskite single cells and the tandem cells were investigated using field-emission scanning electron microscopy (FE-SEM) at an acceleration voltage of 10 kV (FEI, Inspect F). The optical properties of the semi-transparent perovskite devices were characterized with an optical spectrometer (HR2000CG + UV-NIR, Ocean Optics, Inc.). The current density\\u2013voltage (j\\u2013V) curves were measured using a Keithley 2400 SourceMeter and a class-A solar simulator (Yamashita Denso, YSS-50A) equipped with a 180 W xenon lamp. The illumination intensity was calibrated to AM 1.5G 1 sun (100 mW cm\\u22122) using National Renewable Energy Laboratory (NREL)-calibrated silicon solar cells with KG-2 and BK-7 filters (PV Measurements, Inc.) for PSC and CISe devices, respectively. The j\\u2013V curves of the perovskite and tandem solar cells were measured with a 100 ms delay time between adjacent data point acquisition in backward and forward scan modes, respectively. The external quantum efficiencies (EQEs) of the cells were measured with an incident photon-to-current conversion measurement system G1218a (PV Measurements, Inc.) at a chopping frequency of 4 Hz. The EQE spectra of sub-cells in tandem devices were extracted under highly unbalanced photocurrent conditions using additional light sources with controlled wavelengths. Specifically, the EQE of top cells was measured by saturating the bottom cell current with infrared light applying a long-wave pass filter (RG-830 Filter Glass, 830FG07-25, Andover Corporation), whereas EQE of bottom cells was measured by saturating the top cell current with blue light applying a bandpass filter (S-8612 Filter Glass, S86FG11-25, Andover Corporation). All the j\\u2013V and EQE characterizations were carried out under ambient conditions without encapsulations or anti-reflection coatings.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 13,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.22,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Starting materials were all available commercially and used without further purification if not mentioned specially. PbI2 was obtained from Sigma-Aldrich. Hydroiodic acid (AR, 45 wt% in water) and methylamine (AR, 27% in methanol) were purchased from Sinopharm Chemical Reagent Co. Ltd. Sodium tert-butoxide (t-BuONa) was supplied by Aladdin. N,N\\u2032-dimethylformamide (DMF) and chlorobenzene are got from Alfar Aesar. Spiro-OMeTAD was obtained from Luminescence Technology Corp. 2-dicyclohexylphosphino-2\\u2032,4\\u2032,6\\u2032-trisopro -pylbiphenyl (xphos) was purchased from Beijing HWRK Chem Co. Palladium acetate, p-bromoaniline, 4-methoxyiodobenzene, triphenylamine, 2,3-Dihydroxynaphthalene and o-phenylenediamine were got from Tianjin Xiensi Biochemical technology Co.LTD. Other reagents were supplied by Tianjin Guangfu Fine Chemical Research Institute, such as N-Bromosuccinimide (NBS), 1,10-phenanthroline, cuprous chloride and o-xylene. CH3NH3I3 were synthesized according to literatures .\\n\\n1H and 13C NMR spectra were recorded with an INOVA 400 MHz spectrometer (Varian, USA) and AVANCE III 600 MHz spectrometer (Bruker, Switzerland). Mass spectra (MS) were performed on a Autoflex tof/tof III mass spectrometer (Bruker, Germany). UV\\u2013visible spectra of the HTMs in tetrahydrofuran (THF) solutions (1 \\u00d7 10\\u22125mol/L) were recorded with Thermo Evolution 300 UV\\u2013vis spectrometer (Thermo Electron, USA) in the 200\\u2013800 nm wavelength range at room temperature. Thermo gravimetrical analyses (TGA) were recorded with TA Q500 thermo gravimetric apparatus (TA Instruments, USA) at a heating rate of 10 \\u00b0C/min under nitrogen atmosphere. Differential scanning calorimetry (DSC) was conducted on TA Q20 Instrument (TA Instruments, USA) at a heating rate of 10 \\u00b0C/min under nitrogen atmosphere. Photoemission yield spectroscopy (PYS) instrument was PYS-202 ionization energy test system (Sumitomo Heavy Industries, Japan) at the voltage of 100 V, waiting time of 1 s and energy range from 4.0 to 8.5 eV. The time-of-flight (TOF) measurements were performed on TOF401 (Sumitomo Heavy Industries. Ltd. Japan), for which the samples were prepared through spin coating using a structure ITO/HTM (about 1 \\u00b5m)/Al (150 nm) with an active area of 3 \\u00d7 10 mm2. Surface morphology of the TiO2/CH3NH3PbI3/HTM/Au film was obtained using a scanning electron microscope (SEM, XL30S-FEG, FEI, USA). The film thickness was performed on a surface profiler (P-6, KLA-Tencor, USA).\\n\\nN,N\\u2032-diphenyl-4-bromoaniline (1): Triphenylamine (7.41 g, 30.00 mmol) and NBS (5.61 g, 31.50 mmol) were dissolved in 80 mL CCl4. The solution was heated to reflux for 5 h. The precipitated succinimide was filtered while hot, and the solvent was evaporated from the solution, getting light yellow oil. After recrystallization from dry ethanol, the desired product was obtained as a white powder, yielding 6.81 g (70%). Mp: 103\\u2013106 \\u00b0C. 1H NMR (600 MHz, CDCl3) \\u03b4: 7.35\\u20137.29 (m, 2H), 7.24 (d, J = 7.6 Hz, 4H), 7.06 (d, J = 8.1 Hz, 4H), 7.04\\u20136.96 (m, 2H), 6.93 (dd, J = 10.7, 3.7 Hz, 2H).\\n(4-Bromo-phenyl)-di-p-methoxyaniline (2): In a 500 mL four-necked flask equipped with a mechanical stirrer, thermometer and water segregator, all under an argon atmosphere, 4-methoxyiodobenzene (29.30 g, 125.00 mmol), p-bromoaniline (8.60 g, 50.00 mmol) and 1,10-phenanthroline (1.80 g, 10.00 mmol) were added. 300 mL toluene was added and the reaction mixture was then heated to 100 \\u00b0C, at which point potassium hydroxide flake (22.40 g, 400.00 mmol) and cuprous chloride (1.00 g, 10.00 mmol) were added. Then the mixture was heated to reflux for 12 h. The mixture was cooled to room temperature and extracted with ethyl acetate. The organic phase was combined and dried by MgSO4. After filtrating the MgSO4 and removing the solvent by reduced pressure distillation, the residue was purified by column chromatography on silicagel eluting with petroleum ether to give white product 11.41 g (59%). 1H NMR (400 MHz, CDCl3) \\u03b4: 7.27\\u20137.17 (m, 2H), 7.03 (d, J = 8.7 Hz, 4H), 6.80 (dd, J = 12.2, 8.8 Hz, 6H), 3.79 (s, 6H); 13C NMR (100 MHz, CDCl3) \\u03b4: 156.08, 147.94, 140.58, 131.78, 126.59, 122.00, 114.81, 112.38, 55.50.\\nPhenonaphthazine (3): 2,3-dihydroxynapthalene (10.00 g, 62.50 mmol) and 1,2-phenylenediamine (6.75 g, 62.50 mmol) were placed into a round bottom flask under nitrogen atmosphere. 60 mL N,N\\u2032-dimethylaniline was added and mixture was heated to reflux for 4 h. After cooling to room temperature, suitable toluene was added and solid was collected by vacuum filtration. After washing with ethanol (100 mL) and hexane (50 mL) repeatedly, the product was dried under vacuum to yield 9.20 g (64%) of light yellow lamellar crystal. 1H NMR (400 MHz, DMSO) \\u03b4: 8.11 (s, 2H), 7.16 (dd, J = 5.9, 3.3 Hz, 2H), 6.90 (s, 2H), 6.34 (s, 2H), 6.23 (s, 2H), 6.17 (s, 2H). 13C NMR (100 MHz, DMSO) \\u03b4: 134.95, 132.88, 131.25, 125.23, 123.26, 120.64, 112.13, 104.72.\\nBPZTPA: Phenonaphthazine (0.93 g, 4.00 mmol), N,N\\u2032-diphenyl-4-bromoaniline (2.85 g, 8.80 mmol), t-BuONa (0.96 g, 10.00 mmol), xphos (0.26 g, 0.50 mmol) and o-xylene (120 mL) were all placed into a round bottom flask under a nitrogen atmosphere. After the mixture was dissolved, palladium acetate (0.03 g, 0.14 mmol) was added into flask quickly. Then mixture was heated to reflux for 6 h. When cooled to room temperature and added 200 mL water, the reaction liquid was extracted ethyl acetate. The organic phase was combined and dried by MgSO4, leaving brown sticky liquid. After removing the solvent by reduced pressure distillation, the residue was purified by column chromatography on silicagel eluting with CH2Cl2:petroleum ether (1:6) to give yellow product 1.40 g (49%). 1H NMR (400 MHz, DMSO) \\u03b4 7.59 (s, 2H), 7.39 (d, J = 6.7 Hz, 6H), 7.32 (s, 4H), 7.21 (d, J = 7.0 Hz, 6H), 7.13 (d, J = 7.2 Hz, 6H), 7.06 (s, 4H), 7.00 (s, 2H), 6.85 (s, 2H), 6.42 (s, 2H), 5.76 (s, 4H). MS (MALDI-TOF): m/z calcd for C52H38N4: 718.31 [M\\u2212]; found [M\\u2212] 718.29.\\nMeO-BPZTPA: MeO-BPZTPA was obtained from phenonaphthazine and (4-bromo-phenyl)-di-p-methoxyaniline by following the same procedure as that used to make BPZTPA, giving yellow solid (43%). The residue was purified by column chromatography on silicagel eluting with CH2Cl2:petroleum ether (1:2). 1H NMR (400 MHz, DMSO) \\u03b4: 7.19 (t, J = 7.5 Hz, 12H), 7.10 (d, J = 3.2 Hz, 2H), 6.97 (t, J = 9.8 Hz, 12H), 6.93 (d, J = 5.5 Hz, 2H), 6.36 (d, J = 3.4 Hz, 2H), 5.84 (s, 2H), 5.74 (dd, J = 5.5, 3.5 Hz, 2H), 3.75 (d, J = 8.6 Hz, 12H). MS (MALDI-TOF): m/z calcd for C56H46N4O4: 838.35 [M\\u2212]; found [M\\u2212] 838.35.\\n\\nSubstrates were fluorine-doped tin oxide conducting glass (FTO, Pilkington, thickness 2.2 mm, sheet resistance 14 \\u03a9/square). Before used, patterned FTO glass was cleaned with mild detergent, rinsed with distilled water for several times and subsequently with ethanol in an ultrasonic bath, finally dried under air stream. For fabricating the device, TiO2 compact layer and mesoporous TiO2 layer were deposited on FTO glass in turn as reported . And the CH3NH3PbI3 perovskite film was subsequently deposited on the mesoporous TiO2 film by using a modified two-step method according to the literatures . For a deposition of HTM layer, BPZTPA or MeO-BPZTPA in chlorobenzene solution was prepared. HTMs were spin-coated on the mesoporous TiO2/CH3NH3PbI3 film at 2500 rpm for 30 s, and finally an 80 nm-thickness Au layer (Sigma-Aldrich) was deposited on the top of the HTM layer by thermal evaporation under 10\\u22126torr vacuum conditions.\\n\\nFor current density\\u2013voltage (J\\u2013V) characteristics, the cells were illuminated under 100 mW/cm2 (AM 1.5 G) by an Oriel solar simulator 91160A calibrated with a standard Si reference cell (National Institute of Metrology, China), and the J\\u2013V characteristics of the cells were recorded on Keithley 2602 SourceMeter. A mask with a window of 0.10 cm2 was clipped to define the active area of the cell. The monochromatic incident photon-to-electron conversion efficiency (IPCE) spectrum was obtained on a lab-made IPCE testing system . Electrochemical impedance spectra (EIS) of the perovskite solar cells were determined by a ZAHNER IM6e electrochemical workstation (Zahner, Germany) in the dark in the frequency ranging from 0.1 to 105 Hz at the applied bias voltage from 400 to 950 mV with a perturbation amplitude of 10 mV. The obtained impedance spectra were fitted with Zview software based on an appropriate equivalent circuit.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 90.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 45.0,\\n HTL_stack_sequence: BPZTPA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Copper (II) chloride anhydrous (CuCl2) (99%, Acros Organics), zinc acetate dehydrate (Zn (CH3COO) 2\\u22c52H2O, AR), tin (II) chloride dihydrate (SnCl2\\u22c52H2O, AR), thiourea (SC(NH2)2, AR), N,N-dimethylformamide (DMF, AR), ethanol (AR) and dimethylsulfoxide (DMSO, AR) were purchased from Sinopharm Chemical Reagent Co., Ltd. Phenyl-C61-butyric acid methyl ester (PCBM) and bathocuproine (BCP) were obtained from Xi'an Polymer Light Technology Corp. PbI2 and chlorobenzene (99%, Sigma-Aldrich), PEDOT:PSS (Clevios\\u2122 PH 1000), and ITO-coated sheet glasses (<15\\u202f\\u03a9/sq, Nippon Sheet Glass Co.) were commercially obtained. All chemicals were used without further purification.\\n\\nCZTS precursor solution was prepared by sequentially dissolving CuCl2 (3.6\\u202fmmol), SnCl2\\u22c52H2O (1.8\\u202fmmol), ZnAc2\\u22c52H2O (1.8\\u202fmmol) and thiourea (10.8\\u202fmmol) in 6\\u202fml\\u202fN,N-dimethylformamide (DMF) solvent under stirring at 50\\u202f\\u00b0C. The precursor film was spin-coated (2000\\u202frpm, 30\\u202fs) once on patterned and cleaned ITO substrate (4\\u202f\\u00d7\\u202f16\\u202fmm2) and annealed at 300\\u202f\\u00b0C for 5\\u202fmin on a hot-stage in N2 atmosphere, which is referred to as one RSCA cycle number (n). Increasing n leads to the desired CZTS film thicknesses. Note, an excess amount of thiourea is used for the purpose to get the CZTS films with a composition close to stoichiometry, because a serious sulfur loss may occur during thermal decomposition [].\\n\\nMAPbI3 (1.25\\u202fM) precursor solution was prepared by dissolving PbI2 and CH3NH3I with a molar ratio of 1:1 in a mixture solvent of DMF:DMSO (3:1 v/v) under stirring overnight at 65\\u202f\\u00b0C, for which the CH3NH3I was synthesized in our group [].\\nFirst, the MAPbI3 precursor solution was spin-coated onto the CZTS film surface by sequential two rotating steps (first step: 1000\\u202frpm for 10\\u202fs; second step: 4000\\u202frpm for 30\\u202fs), where 350\\u202f\\u03bcL chlorobenzene (CB) as anti-solvent was dripped onto the rotating substrate during the second rotating step; after the spin-coating, the MAPbI3 film was subjected to a thermal annealing at 100\\u202f\\u00b0C for 15\\u202fmin. The PCBM layer was spin-coated from a solution (20\\u202fmg/ml in chlorobenzene) onto the MAPbI3 layer (2000\\u202frpm, 30\\u202fs) and annealed at 80\\u202f\\u00b0C for 10\\u202fmin. Afterwards, the BCP solution (0.5\\u202fmg/ml in ethanol) was spin-coated (4000\\u202frpm, 30\\u202fs) to form a BCP layer over the PCBM layer. Then, Ag electrode (100\\u202fnm in thickness) was deposited onto the BCP surface by thermal evaporation under vacuum (5\\u202f\\u00d7\\u202f10\\u22124\\u202fPa) through a shadow mask, and the overlapped area of 1\\u202f\\u00d7\\u202f4\\u202fmm2 between the Ag and ITO electrodes defined the effective area of the solar cell. Finally, the solar cells were encapsulated in a glove box under N2 atmosphere (O2\\u202f<\\u202f1\\u202fppm, H2O\\u202f<\\u202f1\\u202fppm). Note, the BCP layer in our devices mainly acts as an electrode interfacial layer to improve the fill factor of devices [].\\n\\nThe X-ray diffraction (XRD) patterns of the films were measured on a MXP18AHF X-ray diffractometer with a monochromated Cu K\\u03b1 irradiation (\\u03bb\\u202f=\\u202f1.54056\\u202f\\u00c5), while their Raman spectra were recorded on a Labram-HR Jobin-Yvon spectrometer with 514.5\\u202fnm wavelength incident laser light. The film morphology was characterized by scanning electron microscopy (SEM) (FEI, Sirion 200). The composition of CZTS film was studied by X-ray photoelectron spectroscopy (XPS) using an Al K\\u03b1 X-rays as excitation source (ESCALAB 250, Thermo VG-Scientific), and all the XPS peaks were calibrated by using C1s (284.60\\u202feV) as the reference. The UV\\u2013vis absorption spectra and band gap of samples were measured on a Shimadzu UV-2550 spectrophotometer, while a UV\\u2013Vis\\u2013NIR spectroscopy (Shimadzu, 3700 DUV) was used to determine the absorption coefficient of CZTS film. The current-voltage (J\\u2212V) characteristics and incident photon-to-current efficiency (IPCE) spectra of solar cells were measured as descried elsewhere []. The effective illumination area during the J\\u2212V measurements was restricted to the effective area (i.e., 0.04\\u202fcm2) of each solar cell by a shadow mask.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: CZTS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals were used as received and were used without further purification unless otherwise stated, including PbI2 (99%, Sigma-Aldrich), MABr (99%, DYESOL), FAI (>99%, Greatcell), N, N-dimethylformamide (DMF, 99.8%, Sigma-Aldrich), Dimethyl sulfoxide (DMSO, 99.8%, Sigma-Aldrich), isopropanol (IPA, 99.9%), Tin oxide colloidal solution (SnO2, 15\\u00a0wt% in H2O, Alfa Aesar), 2,2\\u2032,7,7\\u2032-tetrakis (N, N-di-pmethoxyphenylamine) 9,9\\u2032-spirobifluorene (Spiro-OMeTAD, 99.8%, Borun New Material Technology), chlorobenzene (Sigma-Aldrich), bis(trifluoromethane) sulfonamide lithium salt (Li-TFSI, Sigma-Aldrich), acetonitrile (J&K), 4-tert-Butylpyridine (tBP, 98%, Aldrich). Polyethylene naphthalate (PEN)/ITO substrate (Peccell, Japan). PbI2 (1.3\\u00a0M) and FAI (0.85\\u00a0M) were first dissolved in a mixed solvent of DMF: DMSO\\u00a0=\\u00a04:1 (v/v) to form perovskite precursor and MABr (8\\u00a0mg) was dissolved in 1\\u00a0ml IPA to form MABr solution. These solutions were heated at 70\\u00a0\\u00b0C and stirring overnight just before use. The solution of hole transport material was achieved by dissolving 80\\u00a0mg of Spiro-OMeTAD in 1\\u00a0ml chlorobenzene containing 17.5\\u00a0\\u03bcL lithium Li-TFSI in acetonitrile (520\\u00a0mg/mL) and 28.8\\u00a0\\u03bcL 4-tert-butylpyridine (4-tBP).\\n\\nPlanar heterojunction flexible PSCs were fabricated with a configuration of PEN/ITO/SnO2/perovskite/Spiro-OMeTAD/Au. PEN/ITO was used as the substrate. The flexible PEN/ITO films were pasted onto the glass substrates for the following experiments. A 3.75\\u00a0wt% suspension of SnO2 nanoparticles was directly spin-coated onto flexible PEN/ITO substrates, spun at 3000\\u00a0rpm for 30s. Afterwards, spin-coated SnO2 films were annealed at 90\\u00a0\\u00b0C for 60\\u00a0min before the deposition of perovskite films.\\nTo form FA1-xMAxPbIyBr3-y perovskite films, the perovskite precursor was spin-coated on the substrate at 3000\\u00a0rpm. The MABr solution of 100\\u00a0\\u03bcL was then added to the precursor film during the spinning process in a glovebox filled with nitrogen. Subsequently, these films were annealed at 40\\u00a0\\u00b0C, 70\\u00a0\\u00b0C, 100\\u00a0\\u00b0C, 120\\u00a0\\u00b0C and 150\\u00a0\\u00b0C for 40\\u00a0min. The Spiro-OMeTAD precursor solution of 40\\u00a0\\u03bcL was spin-coated onto the cooled perovskite films at 4000\\u00a0rpm for 30s. Finally, 100\\u00a0nm of Au electrode was deposited on the substrates by thermal evaporation. All the preparative work to deposit perovskite and Spiro-OMeTAD was done inside a N2-filled glovebox. For the fabrication of Space-charge-limited current method devices, NiOx films were prepared at room temperature according to a previous report []. The purpose of using hole-only devices (PEN/ITO/NiOx/perovskite/Spiro-OMeTAD/Au) is to prevent perovskite layer from changing its properties due to secondary heating.\\n\\nX-ray diffraction (XRD) patterns of FA1-xMAxPbIyBr3-y films on glass substrates films were detected by a Bruker D8 Advance diffractometer with Cu K\\u03b1 radiation (\\u03bb\\u00a0=\\u00a01.5418\\u00a0\\u00c5) and LYNXEYE_XE detector. A FEI Inspect F50 electron microscope field-emission electron microscope (SEM) was used to acquire surface morphology images of samples. The electron energy is 10\\u00a0keV. Steady-state photoluminescence (PL) and Time-resolved photoluminescence measurement were conducted by using FluoTime 300 (PicoQuant). The space-charge-limited current (SCLC) measurements were carried out by Keithley 2400 digital source-meter under dark condition. The J-V curves of the PSCs devices were measured using a Keithley 2400 series digital source-meter unit under simulated AM 1.5G irradiation (100\\u00a0mW/cm2, xenon-lamp, Newport). The effective area of one cell is 0.09\\u00a0cm2. Electrical impedance spectroscopy (EIS) was obtained by Zahner Ennium electron chemical work-station (ZAHNER ENNIUM Pro). Infrared thermal imaging was photographed by Flir C2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: PEN | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAxMAxPbBrxIx,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25; 25,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials were used directly without any purification, including PbI2 (99%, Xi'an Polymer Light Technology Corp.), CH3NH3I (99%, Jingge, Wuhan), N,N-dimethylformamide (99.8%, J&K Scientific), PEDOT:PSS (Baytron, PVP AI 4083), Fullerene derivative [6,6]-phenyl C61-butyric acid methyl ester (PC61BM, Xi'an Polymer Light Technology Corp.), chlorobenzene (99.8%, J&K Scientific), and methylamine ethanol solution (30%, Sinopharm).\\n\\nFig. 1 presents the architecture of PSCs and a schematic diagram of perovskite films prepared by in-situ hot-casting technique (HCT) and MGT. The patterned indium tin oxide (ITO) substrate was ultrasonically cleaned in acetone, detergents/H2O, distilled water, and isopropyl alcohol for 20\\u202fmin sequentially, and was then dried by clean N2 flow and treated by UV-ozone for 20\\u202fmin. The PEDOT:PSS solution was spin-coated at a speed of 3000\\u202frpm for 30\\u202fs, followed by a post-annealing at 150\\u202f\\u00b0C for 15\\u202fmin. The perovskite precursor solution with a concentration of 450\\u202fmg/ml (550\\u202fmg/ml for anti-solvent method) was prepared by mixing PbI2 and CH3NH3I in DMF (the mole ratio CH3NH3I:PbI2\\u202f=\\u202f1:1). It was vigorously stirred at 65\\u202f\\u00b0C for 12\\u202fh and filtered with a 0.22\\u202f\\u03bcm PVDF filter before the use. The deposition of perovskite active layer was performed in air ambient (relative humidity of 60% and the room temperature of 20\\u202f\\u00b0C). The PEDOT:PSS-coated ITO substrate was heated on heating spin-coater for two minutes to ensure the substrate reached the corresponding temperature, and then the mixed precursor solution was spin-coated at 3000\\u202frpm for 30\\u202fs, followed by a heat-treatment at 100\\u202f\\u00b0C for 10\\u202fmin in air. After cooling to room temperature, the raw MAPbI3 perovskite films were simply placed in the CH3NH2 gas environment for 2\\u202fs\\u202fat room temperature [,,]. In an instant, the perovskite films would react with CH3NH2 to form MAPbI3\\u00b7xCH3NH2, which is colorless and transparent in liquid form and would spread over the PEDOT:PSS-coated substrate. Removed to the ambient quickly, CH3NH2 molecules would depart from the intermediate, and perovskite films turned to dark brown and became shiny. It is necessary to point out that the room temperature and methylamine alcohol solution should be controlled at \\u223c20\\u202f\\u00b0C to prevent too rapid volatilization of methylamine gas from the intermediate, which has an adverse effect on morphology of the films. Preparation process of perovskite films is divided into spin-coating at room temperature without methylamine gas treatment (RT-W/O) and with methylamine gas treatment (RT-MGT), in-situ hot-casting without methylamine gas treatment (HCT-W/O) and with methylamine gas treatment (HCT-MGT). The fabrication of perovskite films with anti-solvent method in glove box refers to our previous work []. Subsequently, the PCBM solution with a concentration of 20\\u202fmg/ml was spin-coated onto the perovskite layer at 3000\\u202frpm for 30\\u202fs. Finally, a 100\\u202fnm Ag electrode was deposited via thermal evaporation with a mask, resulting in an active area of 0.09\\u202fcm2.\\n\\nThe UV\\u2013vis spectrophotometer (Puxi, T9, China) and X-ray diffraction (XRD, Rigaku D, Max 2500, Japan) were used to characterize the absorption properties and crystallographic properties of MAPbI3 films, respectively. Scanning electron microscope (FEI Helios Nanolab 600i SEM, America) was employed to characterize the morphology of MAPbI3 thin films. Current density\\u2212voltage (J\\u2212V) characteristics of PHJ\\u2212PSCs were measured by a digital Source Meter (Keithley, model 2420) from \\u22120.2\\u00a0V to +1.2\\u00a0V with a 50\\u00a0ms scanning delay in both reverse- and forward-scan modes. The measurement was carried out by a Xenon-lamp-based solar simulator (Newport 91160s, AM 1.5\\u00a0G) with a light intensity of 100\\u00a0mW/cm2, which was calibrated by a standard silicon solar cell.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> none,\\n Perovskite_deposition_procedure: Spin-coating >> Recrystallization,\\n Perovskite_deposition_thermal_annealing_temperature: 100.0 >> Unknown,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Polytriarylamine (PTAA), methylammonium (MAI,) and fullerene derivative [6,6]-phenyl C61-butyric acid methy ester (PCBM) were purchased from Xi\\u2019an Polymer Light Technology Corporation. Lead iodide (PbI2) was purchased from Tianjin weiyi chemical technology corporation. Three kinds of IT-like NFEAs (ITIC, ITIC-Th and IT-M) were purchased from Solarmer Materials Inc. Zirconium acetylacetonate (ZrAcac) was purchased from Alfa Aesar. Solvents such as N,N-Dimethylformamide (DMF), chlorobenzene (CB) and so on were purchased from J&K Seal (Beijing, China) except the Dimethyl sulfoxide (DMSO) was purchased from Sigma-Aldrich.\\n\\nHere, we used the inverted device configuration as show in Fig. 1 a. Firstly, the indium tin oxide (ITO) substrates were ultrasonically cleaned in acetone, detergents, distilled water and isopropanol (IPA) for 20\\u202fmin, respectively. The ITO substrates dried by nitrogen and treated by UV-ozone for 20\\u202fmin. After that, PTAA solution (6\\u202fmg/ml in toluene) was spin coated upon substrate at 4000\\u202frpm for 30\\u202fs and annealed at 100\\u202f\\u00b0C for 10\\u202fmin. The MAPbI3 film was prepared according to the previous report (Xu et al., 2018), PbI2 (1.2\\u202fM) and MAI (0.3\\u202fM) was firstly dissolved in the mixture of DMF/DMSO (volume ratio\\u202f=\\u202f1:0.1). Then, 60 ul above perovskite precursor solution was deposited on PTAA thin film and spin-coated at 6000\\u202frpm for 20\\u202fs and then 70 ul MAI solution (40\\u202fmg/ml in IPA) was dropped onto the center of the substrates for another 20\\u202fs. At last, the film was placed on the hot plate and annealed at 100\\u202f\\u00b0C for 30\\u202fmin. For preparing ETL, ITIC, ITIC-Th, IT-M and PCBM were dissolved in CB (3, 5, 7 and 9\\u202fmg/ml) and were spin-coated on MAPbI3 layer at 3000\\u202frpm for 30\\u202fs and then annealed at 90\\u202f\\u00b0C for 30\\u202fmin. The thickness of the ETL was controlled by concentration of the precursor solution. Finally, the ZrAcac solution (1\\u202fmg/ml in IPA) was deposited onto the ETL by spin coating at 4000\\u202frpm for 30\\u202fs and then a strip of Ag cathode (100\\u202fnm) was formed via thermal evaporation under a vacuum of 6\\u202f\\u00d7\\u202f10\\u22124 Pa.\\n\\nThe UV\\u2013vis absorbance spectra were measured by UV\\u2013vis spectrophotometer (UV\\u2013vis, Lambda 365, PerkinElmer, USA). The X-ray diffraction (XRD) was measured by XRD test instrument (Bruker D8 Advance, Germany) with a Cu K\\u03b1 radiation source under 40 KV and 44\\u202fmA. The top-view and cross-section scanning electron microscopy (SEM) morphology were measured by scanning electron microscopy (FEI Helios Nanolab 600i, USA). J-V characteristics and monochromatic incident photon-to-electron conversion efficiency (IPCE) were measured by the solar simulator (Enlitech SS-F5-3A, Taiwan). The time resolved PL spectra (TRPL) was measured by fluorescence spectrophotometer (Edinburgh FS 5, China). The contact angle was measured by surface contact angle tester (Zhongchen JC2000D1, China).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ITIC | Zn(acac)2,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 30.0,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Tin (II) iodide (SnI2), PAMS, bathocuproine (BCP), [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), dimethyl sulfoxide (DMSO), N, N-dimethyl formamide (DMF), diethyl ether, chlorobenzene and silver (Ag) pellets were purchased from Sigma-Aldrich Corporation. Formamidinium iodide (FAI) was purchased from Xi\\u2019an Polymer Light Technology Corporation, as used without further purification. The hole-transporting polymer PEDOT: PSS (CLEVIOS P VP AI 4083), i.e. poly(ethylenedioxythiophene) doped with poly(styrenesulfonate), was purchased from Bayer Corporation and used as received. Indium-tin oxide (ITO) coated glass was used as the device substrate, purchased from China Southern Glass Holding Co Ltd with a surface resistance of 10\\u202f\\u03a9/sq. The matrix solvent of the perovskite precursor is DMF and DMSO, with a molar ratio of 4:1. FAI and SnI2 were dissolved in the matrix solvent at the molar ratio of 1:1, with the ultimate concentration kept constant at 1.0\\u202fmol/mL. The FAI-SnI2 precursor solution was stored in the glovebox under dry nitrogen atmosphere before spin-coating. PAMS was dissolved in diethyl ether at a serial weight concentration of 0.3, 0.5, 1.0, 2.0 and 3.0\\u202fmg/mL, used as the antisolution for the modified devices. For simplicity, the devices modified by PAMS antisolution were labeled as Device (0.3), Device (0.5), Device (1.0), Device (2.0) and Device (3.0) corresponding to the blended concentration of PAMS in diethyl ether.\\n\\nPolished ITO glass was thoroughly cleaned before use in ultrasonic solvent bath of detergent, acetone, isopropanol and deionized water in sequence. Surface treatment of oxygen plasma was also performed on the ITO glass to completely remove the organic residues before the spin-coating process. PEDOT: PSS solution was spin-coated on the ITO glass substrate at 3500\\u202frpm and annealed at 130\\u202f\\u00b0C for 30\\u202fmin to form a solid film of around 50\\u202fnm. The precursor solution of FAI: SnI2 was spin-coated on top of PEDOT: PSS layer under the washing of the antisolvent or antisolution, diethyl ether blended with PAMS, to prepare the FASnI3 perovskite film. After the thermal annealing of 15\\u202fmin conducted on the perovskite film of FASnI3, PCBM solution of 30\\u202fmg/mL in chlorobenzene was spin-coated in subsequence to prepare a 50-nm electron-transport layer on top. The whole fabrication process was completed after the thermal evaporation of 10\\u202fnm BCP and 100\\u202fnm Ag on top of the PCBM layer under the high vacuum of 4\\u202f\\u00d7\\u202f10\\u22124 Pa.\\n\\nThe characteristic curves of current density vs voltage (J-V) of the perovskite solar cells were tested under the illumination of 1 sun (100\\u202fmW/cm2) on a solar cell testing system consisting of a computer-programmed sourcemeter (Keithley 2400) and a solar simulator (AM 1.5G, Newport), with the light density of 100\\u202fmW/cm2 calibrated by a standard Si photodiode. The monochromatic incident photon-to-electron conversion efficiency (IPCE) was collected on a calibrated testing system (Qtest Station 1000AD). The thickness of the organic layers was measured using a calibrated surface profiler (Alfa Step-500, Tencor). Top-view surface morphology was studied using scanning electron microscope (SEM, Hitachi S-4800) and atomic force microscope (AFM, Bruker FastScan), respectively. X-ray diffraction (XRD) patterns were collected on a X-ray diffractometer (D8 Advance, Bruker Co.) using monochromatic Cu Source (\\u03bb\\u03ba\\u03b11(Cu)\\u202f=\\u202f0.15418\\u202fnm) at 5.0\\u202fkV. The equilibrium Photoluminescence (PL) spectra were recorded by a steady-state spectrometer (Edinburgh Instruments F900) under the excitation of 520\\u202fnm. Time-resolved photoluminescence (TRPL) spectra were collected on a lifetime and steady-state spectrometer (FLS980, Edinburgh Instruments Ltd.) with the laser wavelength of 479\\u202fnm. The contact angles were recorded on a contact angle measurement (KRUSS DSA20). All the performance characterization was carried out in the ambient atmosphere without any encapsulation of the devices.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: FASnI3,\\n Perovskite_composition_short_form: FASnI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Preparation of 2,7-dibromo-3',6'-difluorospiro[fluorene-9,9'-xanthene] (2Br2F-SFX): A mixture of 2,7-dibromo-9-fluorenone with 10 equiv of 3-fluorophenol in the presence of 4 equiv of methane sulfonic acid was heated at 150\\u202f\\u00b0C for 8\\u202fh. After cooling to room temperature, the mixture was diluted with methanol. Then the white precipitate was filtered and washed with abundant of methanol to afford 2Br2F-SFX as a white solid (yield 64.3%). 1H NMR (600\\u202fMHz, CDCl3, 298K), \\u03b4 (ppm)\\u202f=\\u202f7.62 (dd, J\\u202f=\\u202f8.2, 0.4\\u202fHz, 2H), 7.51 (dt, J\\u202f=\\u202f8.1, 1.8\\u202fHz, 2H), 7.22 (dd, J\\u202f=\\u202f1.8, 0.4\\u202fHz, 2H), 6.95 (dd, J\\u202f=\\u202f9.4, 2.6\\u202fHz, 2H), 6.57 (ddd, J\\u202f=\\u202f8.7, 7.9, 2.6\\u202fHz, 2H), 6.34 (dd, J\\u202f=\\u202f8.8, 6.1\\u202fHz, 2H). 13C NMR (151\\u202fMHz, CDCl3, 298K), \\u03b4 (ppm)\\u202f=\\u202f162.17, 160.56, 158.20, 150.17, 140.34, 134.85, 131.81, 125.56, 124.60, 124.58, 121.37, 121.31, 119.17, 119.01, 116.53, 116.37, 57.42. MALDI-TOF: m/z [M]+ cacld. C25H12Br2F2O, 523.9223; found: 523.9221.\\nPreparation of 3',6'-difluoro-N\\u2019,N\\u2019,N\\u2019\\u2019,N\\u2019\\u2019-bis(4-methoxyphenyl) spiro [fluorene-9,9'-xanthene]-2,7-diamine (2mF-X59): A mixture of 2Br2F-SFX with 2.2 equiv of 4,4'-dimethoxydiphenylamine in the presence of 2.5 equiv of t-BuONa was dissolved into dry toluene under nitrogen atmosphere. Then 0.011 equiv of Pd2(dba)3 and 0.069 equiv of [(t-Bu)3PH]BF4 were put into the mixture solution and refluxed under 120\\u202f\\u00b0C for 10\\u202fh. After cooling to room temperature, the solution was poured into water and extracted with dichloromethane. Solvent was removed by rotary evaporation and the residue was purified by column chromatography with petroleum ether: ethyl acetate (10:1, v:v) as eluent to afford 2mF-X59 as a light yellow solid (yield 42.5%). 1H NMR (600\\u202fMHz, d 6-DMSO, 298K), \\u03b4 (ppm)\\u202f=\\u202f7.59 (d, J\\u202f=\\u202f8.4\\u202fHz, 2H), 7.05 (dd, J\\u202f=\\u202f9.4, 2.6\\u202fHz,2H), 6.89\\u20136.83 (m, 10H), 6.81\\u20136.76 (m, 8H), 6.73 (dd, J\\u202f=\\u202f8.4, 2.2\\u202fHz, 2H), 6.54\\u20136.46 (m, 4H), 3.69 (s, 12H). 13C NMR (151\\u202fMHz, d 8-toluene, 298K), \\u03b4 (ppm)\\u202f=\\u202f163.20, 161.58, 156.49, 156.19, 152.19, 152.11, 149.11, 141.38, 133.01, 126.52, 121.73, 121.50, 120.13, 118.56, 118.49, 115.03, 111.19, 111.05, 104.30, 104.13, 54.84, 54.07. MALDI-TOF: m/z [M]+ cacld. C53H40F2N2O5, 822.2905; found: 822.2902.\\nDevice fabrication: The CsPbI2Br PSCs were prepared with a structure of FTO/TiO2/CsPbI2Br/HTL/Au. FTO/Glass substrates were cleaned with acetone, isopropanol and distilled water in an ultrasonic bath for 30\\u202fmin successively. Then the substrates were treated with UV cleaner for 10\\u202fmin, 40\\u202fnm TiO2 layers were fabricated by chemical bath deposition on cleaned FTO substrates [,]. The substrates were immersed in 200\\u202fml aqueous solution with 4.5\\u202fml Titanium tetrachloride for 60\\u202fmin\\u202fat 70\\u202f\\u00b0C, followed by washing with distilled water and annealing at 200\\u202f\\u00b0C for 30\\u202fmin. The perovskite precursor solution was prepared by mixing CsI, PbI2(DMSO) and PbBr2(DMSO) in DMF/DMSO (9:1, v/v) according to our reported procedure [,]. The concentration of perovskite precursor solution was 0.9\\u202fM. The perovskite solution was spin-coated on top of the TiO2 film in a two-step process, first at 1000\\u202frpm for 10\\u202fs and then at 3000\\u202frpm for 40\\u202fs while 200\\u202f\\u03bcl of chlorobenzene antisolvent was dropped onto the substrate at 15\\u202fs before the end of spinning. For passivation of perovskite film, the F4-TCNQ with different concentration in chlorobenzene was used as antisolvent. After that, the samples were heated at 120\\u202f\\u00b0C for 10\\u202fmin and 200\\u202f\\u00b0C for 2\\u202fmin to obtain black CsPbI2Br films. Spiro-OMeTAD, 2mF-X59 and 2mF-X59\\u00a0+\\u00a0F4-TCNQ were used as HTLs, respectively. To prepare the Spiro-OMeTAD solution, 90\\u00a0mg of Spiro-OMeTAD was dissolved in 1\\u00a0mL of chlorobenzene and mixed with 36\\u00a0\\u03bcL t-BP and 22\\u202f\\u03bcL Li-TFSI (520\\u202fmg/ml) solution in acetonitrile. The Spiro-OMeTAD solution (90\\u202fmg/ml) was spin-coated onto CsPbI2Br layer at 5000\\u202frpm for 30\\u202fs as HTL. 30\\u202fmg of 2mF-X59 without or with F4-TCNQ (1.5\\u202fmg, 5\\u202fwt%) was dissolved in 1\\u202fml of chlorobenzene. The solution of HTLs was spin-coated on top of the perovskite films at 5000\\u202frpm for 30\\u202fs. Then the 2mF-X59 films were heated at 90\\u202f\\u00b0C for 10\\u202fmin. Finally, a gold layer (~80\\u202fnm) was evaporated on the top of device as anode and a shadow mask is applied to form the device active area of 0.09\\u202fcm2.\\nDevice characterization: Top-view and cross-sectional SEM images of CsPbI2Br PSCs were characterized by a HITACHI, SU-8020 microscope. The absorption spectra were obtained by using a UV/Vis NIR spectrophotometer (Per-kinElmer, Lambda 950). XRD patterns were conducted on a D/MAX 2400 diffractometer with Cu Ka radiation (Rigaku). PL (excitation at 532\\u202fnm) spectra were obtained by using a FLS980 spectrometer (Edinburgh Instruments Ltd) and TRPL spectra were measured with a PicoQuant FluoQuant 300. Water contact angles of films were observed using a Dataphysics OCA 20. The band structure of the HTL films were analyzed using ultra-violet photoelectron spectra (UPS, ESCALAB 250Xi, Thermo Fisher). XPS analysis of the perovskite films is carried out by using a photoelectron spectrometer (ESCALAB250Xi, Thermo Fisher Scientific). The J-V curves of the CsPbI2Br PSCs were performed on Keithley 2400 source under ambient condition. The illumination intensity was calibrated to 100\\u202fmW/cm2 by a National Renewable Energy Laboratory (NREL)-traceable KG5-filtered silicon reference cell. The external quantum efficiency (EQE) of the CsPbI2Br PSCs was measured by using a QTest Station 2000ADI system (Crowntech Inc.), including a tungsten-halogen lamp, a Si detector and a monochromator.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBrI2,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120; 200,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 2.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"First, the precursor solutions were prepared in the following. Hole transporting material precursor solution was prepared by mixing (Poly (3,4-ethylenedioxythiophene) poly styrenesulfonate, PEDOT:PSS) with methanol at a volumetric ratio of 1:1. The mixed solution was sonicated at 30\\u202fmin in ambient condition. The PbI2 precursor solution was prepared by dissolving 460\\u202fmg/ml in dimethylformamide (DMF) at concentration of 1\\u202fM and kept at 70\\u202f\\u00b0C. Then, 50\\u202fmg of MAI (CH3NH3I) dissolved in 1\\u202fml of isopropanol (IPA) at room temperature. Electron transporting material precursor solution was prepared by dissolved ([6,6]-Phenyl C61 butyric acid methyl ester, PCBM) in chlorobenzene with concentration of 30\\u202fmg/ml. The PCBM solution was stirring at 70\\u202f\\u00b0C for overnight.\\nThen, the devices were fabricated in the following. A struture and energy band diagram of p-i-n perovskite solar cell (Fluorine doped Tin Oxide (FTO)/PEDOT:PSS/CH3NH3PbI3/PCBM/Ag) are shown in Fig. 1(a) and 1(b), respectively. The perovskite thin film was prepared on a FTO substrate (with sheet resistance of 7\\u202f\\u03a9/sq). The FTO glass substrate was patterned using Zn metal and mixtures of HCl and deionized (DI) water (1:1). The patterned FTO glass was cleaned under sonicator with solution of Alconox cleaning detergents, DI water, acetone and isopropanol for 15\\u202fmin each, respectively. It was dried with flowing N2. Then, surface treatment was performed by ultraviolet ozone for 30\\u202fmin.\\nThe hole transporting layer (PEDOT:PSS precursor solution) was deposited on the patterned FTO substrate using spin-coating deposition with speed of 3000\\u202frpm for 60\\u202fs and followed by annealing at 150\\u202f\\u00b0C for 15\\u202fmin. After cooling down to room temperature, it was transferred to a low relative humidity (<20%) in a N2 filled glove box for perovskite layer preparation. The perovskite layer was formed using two-steps spin-coating deposition.\\nThe PbI2 precursor solution was firstly spin-coated on the PEDOT:PSS layer at 3000\\u202frpm for 30\\u202fs. Subsequently, the PbI2 film was annealed at 70\\u202f\\u00b0C for 15\\u202fmin. Two sets of PbI2 layer and MAI solution was divided at non-heat and pre-heat before spin-coating process. The modified sequential method are summarized in Fig. 2 (where NN refers to both non-heat of PbI2 film and MAI solution, NH refers to non-heat of PbI2 film but pre-heat of MAI solution, HN refers to pre-heat of PbI2 film but non-heat of MAI solution, and HH refers to both pre-heat of PbI2 film and MAI solution). The PbI2 film was coated by the MAI solution using spin-coating deposition at 2000\\u202frpm for 30\\u202fs, and annealed at 100\\u202f\\u00b0C for 120\\u202fmin for perovskite crystalization. After cooling down to room temperature, the PCBM precursor solution was spin-coated on the perovskite layer at 2000\\u202frpm for 30\\u202fs. Finally, the Ag back contact was deposited on the top of device using thermal evaporation.\\n\\nThe film morphology investigation was performed using the field emission scanning electron microscope (FE-SEM, JEOL JSM-6335F) operating at a voltage of 15.0\\u202fkV. The XRD (X-ray diffraction) patterns were measured by a Rigaku miniflex II diffractometer with Cu K\\u03b1 X-ray radiation source in the reflection geometry in the range of 10\\u201360\\u00b0 at a step size of 0.01\\u00b0 in 2\\u03b8 mode. The photoluminescence and time-resolved photoluminescence spectra were measured using photoluminescence spectrometer. Photovoltaic characteristics were measured under standard simulated solar radiation of 100\\u202fmW/cm2 (AM1.5) with an active area of 0.04\\u202fcm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: 15.0 >> 120.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The photoactive materials comprising PbI2 (99.999% purity) and CH3NH3I were purchased from Lumtec and Dyesol respectively. Chlorobenzene and DMF were obtained from Sigma, while PC70BM was acquired from 1-material. Poly(3,4-ethylenedioxythiophene)\\u2013poly(styrenesulfonate) (PEDOT:PSS, Al 4083) was purchased from Ossila. Spherical Ag NPs at a concentration of 4.73 mg mL\\u22121 (silver basis) and a particle concentration of 5.2 \\u00d7 1012 particles mL\\u22121 were obtained from nanoComposix. The Ag NPs have Ag core diameters of approximately 50 nm, are dispersed in DI water and have surface polyvinylpyrrolidone (PVP) groups. Spherical SiO2 NPs with a concentration of 10.4 mg mL\\u22121 (silica basis) and a particle concentration of 9.1 \\u00d7 1013 particles mL\\u22121 were also obtained from nanoComposix. The SiO2 NPs also have silica core diameters of approximately 50 nm, are dispersed in DI water and have surface silanol groups. These were all used as received. Patterned indium tin oxide (ITO) glass substrates measuring 12 \\u00d7 12 mm were obtained from Lumtec. Reference photovoltaic devices were fabricated in the inverted structure of \\u201cITO/PEDOT:PSS/CH3NH3PbI3/PCBM/Ag\\u201d.\\n\\nITO glass substrates were cleaned by ultrasonication for 10 minutes in 2% Hallmanex detergent, DI water, acetone and isopropanol. The PEDOT:PSS solution was first filtered through a 0.45 \\u03bcm PVDF filter and ultrasonicated for 1 minute. Ag or SiO2 NPs from stock solution were first diluted in DI water before blending into the PEDOT:PSS solution to reach the desired concentration. The resulting blend was ultrasonicated for 1 minute. The optimized concentration (for highest efficiency) of Ag or SiO2 NPs in the PEDOT:PSS blend was 1011 Ag or SiO2 particles mL\\u22121 with a water content of 5%. In both types of devices, PEDOT:PSS hole transport layers (or blends with Ag NPs) were formed via spin coating on ITO coated glass at 4000 rpm for 30 s, resulting in approximately 20 nm thick layers. After spin-coating, the films were immediately transferred onto a hotplate for annealing at 120 \\u00b0C for 15 minutes. The CH3NH3PbI3 device was fabricated via a gas-assist method on top of the PEDOT:PSS film. CH3NH3PbI3 DMF solution was prepared from lead iodide (PbI2) and CH3NH3I (MAI) at a precursor concentration of 1 M. This solution was pipetted onto the substrate and spin-coated at 2500 rpm. A dry N2 gas stream was blown over the film for 9 seconds after spin-coating had begun. The films were then annealed at 100 \\u00b0C for 10 minutes. Next, the PC70BM electron transport layer was prepared by dissolving PC70BM in chlorobenzene at 20 mg mL\\u22121 and subsequently spin-coated at 3000 rpm to form a 40 nm thick film. Device fabrication was completed by thermal evaporation of a 100 nm silver electrode at a background pressure of 10\\u22125 mbar. For all devices, a cell area of 0.13 cm2 was defined during thermal evaporation via a shadow mask. Devices were stored in a N2 purged glovebox after fabrication.\\n\\nLight absorption of the full device was measured using a Perkin Elmer UV-vis spectrometer (Lambda 1050). The absorption profile includes absorption from the ITO layer as well as other layers which may not contribute to the photocurrent generated. The external quantum efficiency (EQE) was determined using a QEX10 spectral response system (PV measurements, Inc.). The thicknesses of various materials used were estimated using a KLA Tencor D-600 Stylus Profiler with sub-Angstrom resolution. Current density\\u2013voltage (J\\u2013V) measurements were obtained from an IV5 solar cell I\\u2013V testing system (PV measurements, Inc.) using a Keithley 2400 source meter and illumination at 100 mW cm\\u22122 by an AM 1.5G solar simulator (Oriel model 94023A). Series and shunt resistances were estimated from the slope of the J\\u2013V curve at the open circuit voltage and short circuit current. For hysteresis studies, the J\\u2013V characteristics were measured at low scan rates of 0.01 V s\\u22121. Atomic force microscope (AFM) images were taken using a Bruker dimension icon SPM. Images of the surface topology were captured via Carl Zeiss AURIGA Cross Beam scanning electron microscopy (SEM). X-ray diffraction (XRD) results were obtained with CuK\\u03b1 radiation and by step-scanning at a step size of 0.02\\u00b0. Impedance spectroscopy was performed via an Autolab PGSTAT-30 equipped with a frequency analyzer module in the frequency range of 1\\u2013106 Hz. The AC amplitude was set to 20 mV (rms) to maintain the linearity of the response. The impedance was recorded at 0.9 V forward bias under light and dark conditions in a N2 purged glove box. The lamp used to measure impedance under light conditions was calibrated to resemble the power output of the light source of the I\\u2013V testing system. The flat-band potential was estimated from Mott\\u2013Schottky curves at 10 kHz frequency. Nova software was used to model impedance spectra. J\\u2013V, EQE and absorption measurements were performed in air within 2 days of fabrication to minimize the effects of device degradation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-70,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.13,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite solar cells are fabricated on F-doped SnO2 substrates. The patterned FTO glasses are sequentially cleaned with deionized water, ethanol, and acetone in an ultrasonic bath. After being dried, the FTO glasses are ultraviolet-ozone treated for 15\\u202fmin. A compact TiO2 layer is deposited onto the FTO glasses by spin-coating titanium diisopropoxide bis(acetylacetonate) (0.15\\u202fM in 1-butanol) twice at 3000\\u202frpm for 30\\u202fs, and dried at 150\\u202f\\u00b0C for 30\\u202fmin in the air. The obtained TiO2 compact layer is annealed at 500\\u202f\\u00b0C for 30\\u202fmin. A mesoporous TiO2 scaffold layer is spin-coated onto the compact TiO2 layer at 5000\\u202frpm for 30\\u202fs using a homemade TiO2 paste, and annealed at 500\\u202f\\u00b0C for 30\\u202fmin. The obtained TiO2 film is further treated with 40\\u202fmM TiCl4 aqueous solution at 70\\u202f\\u00b0C for 30\\u202fmin, and sequentially annealed at 500\\u202f\\u00b0C for 30\\u202fmin.\\nPerovskite films are prepared using the one step antisolvent method in a nitrogen filled glovebox. 1\\u202fmmol PbI2, 1\\u202fmmol MAI, x mmol GuSCN, and 1\\u202fmmol dimethyl sulfoxide (DMSO) are added into 1\\u202fmL dimethyl formamide (DMF), followed by stirring at 70\\u202f\\u00b0C for one night to obtain a clear solution. The GuSCN concentration varies from 0\\u202fmmol to 0.20\\u202fmmol with a step size of 0.05\\u202fmmol, i.e., the mole ratio of GuSCN to PbI2 is 0, 5%, 10%, 15% and 20%, the corresponding perovskite films and perovskite solar cells are referred as Gu00 (the pristine MAPbI3), Gu05, Gu10, Gu15, and Gu20, respectively in the following context. 50\\u202f\\u03bcL perovskite precursor solution is spin-coated onto the TiO2 film (1000\\u202frpm for 10\\u202fs, 5000\\u202frpm for 20\\u202fs), after spinning at 5000\\u202frpm for 6\\u202fs, 450\\u202f\\u03bcL chlorobenzene is quickly added to the film. The obtained perovskite films are further dried at 100\\u202f\\u00b0C for 30\\u202fmin.\\nHole transport material containing 72.3\\u202fmg Spiro-OMeTAD (Xi'an Polymer Light Technology Corp.), 28.5\\u202f\\u03bcL 4-tert-butylpyridine (TBP), 17.5\\u202f\\u03bcL lithium bis(trifluoromethanesulfonyl)imide (LiTFSI, 520\\u202fmg of LiTFSI in 1\\u202fmL acetonitrile) in 1\\u202fmL chlorobenzene is spin-coated onto the perovskite film at 3000\\u202frpm for 30\\u202fs, and kept in a desiccator over night before deposition of the metal electrode. Finally, 100\\u202fnm Ag electrode is thermally evaporated through a metal mask onto the hole transport material.\\n\\nCrystal structure of the MAPbI3 perovskite film with GuSCN additive is determined using X-ray diffraction (SmartLab 9\\u202fkW, Rigaku) with Cu K\\u03b1 radiation. UV\\u2013vis absorption spectrum of the perovskite film is observed on a UV\\u2013vis spectrometer (Lambda 950). Planar view scanning electron microscopy (SEM) is conducted on Hitachi S4800 to check the film morphology of the perovskite films. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) measurements are conducted to check the composition of the perovskite films. The XPS measurement is carried on Thermo Scientific K-Alpha 0.5EV. The FTIR results are obtained using Ncolet IS-50 infrared spectrometer. The simulated sunlight is produced by XEF-300 solar simulator and the light intensity is calibrated to give a standard AM 1.5 light source (100\\u202fmW\\u202fcm\\u22122). The current density-voltage curves of the perovskite solar cells are measured with Keithley 2450 sourcemeter in the ambient atmosphere. The effective area of the solar cells is kept to 0.1\\u202fcm2 with a metal mask. In the reverse scan mode, the applied voltage is scanned from 1.2\\u202fV to \\u22120.2\\u202fV. In the forward scan mode, the applied voltage is scanned from \\u22120.2\\u202fV to 1.2\\u202fV. The scan speed is 10\\u202fmV\\u202fs\\u22121. The stability test is conducted in the ambient atmosphere with humidity around 30%\\u201340%. Between the intervals of two successive measurements, the perovskite solar cells are kept in a desiccator without light exposure. The incident photo-to-electron conversion efficiency (IPCE) measurement is conducted with a quantum efficiency system (QE-R, Enli Technology Co., Ltd) under AC mode. The electron-only device with the structure FTO/TiO2/perovskite/PCBM/Ag is fabricated, and the corresponding dark current-voltage curves are measured from 0.01\\u202fV to 1.3\\u202fV with Keithley 2450 sourcemeter.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 360,\\n Stability_PCE_initial_value: 15.28,\\n Stability_PCE_end_of_experiment: 40,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals and solvents were used as purchased without further purification unless otherwise noted. The solvents dimethylformamide (DMF), dimethyl sulfoxide (DMSO) and chlorobenzene (CB) were dried using molecular sieves (Carl Roth, 3 \\u00c5 type 562 C). PEDOT:PSS was purchased from Heraeus (CLEVIOS\\u2122 P VP AI 4083), [6,6]-phenyl C61 butyric acid methyl ester (PC60BM) from Solenne, phenylethylammonium iodide (PEAI) from Greatcell Solar and aluminium from Kurt J. Lesker Company. All the other chemicals were purchased from Sigma Aldrich. Tin iodide (SnI2) with a purity of 99.99% was further purified in a tube furnace based on the different boiling points of tin(II) iodide and tin(IV) iodide. Under constant moderate N2 flow, the furnace is heated up to 380 \\u00b0C within 30 minutes, kept at this temperature for 2 h and afterwards cooled down to room temperature.\\nPatterned glass/ITO substrates (15 \\u00d7 15 \\u00d7 1.1 mm) (15 \\u03a9 sq\\u22121) from Luminescence Technology Corp. were pre-cleaned with acetone, put in an isopropyl alcohol bath and placed into an ultrasonic bath at 40 \\u00b0C for 30 minutes. The substrates were then dried in an N2 stream and further plasma etched for 3 minutes. PEDOT:PSS (used as purchased) was filtered through a 0.45 \\u03bcm PVDF filter, then deposited by spin-coating at 3000 rpm for 60 s followed by annealing at 120 \\u00b0C for 20 minutes. All steps were done outside of the glove box.\\nThe perovskite precursor solution (1 M) was prepared by dissolving the corresponding amounts of MAI, FAI, PEAI, and SnI2 as well as 10 mol% SnF2 as additive in DMF/DMSO (4/1 vol%) to obtain the theoretical composition MA0.75FA0.15PEA0.1SnI3. The precursor solution was stirred overnight at room temperature under nitrogen atmosphere, followed by filtration through a 0.45 \\u03bcm PTFE filter.\\nThe precursor solution was spin-coated on the glass/ITO/PEDOT:PSS substrates at 5000 rpm for 60 s. After 20 s spinning time, 80 \\u03bcl of CB were dropped on the spinning substrates to crystallize the perovskite, indicated by a color change from pale yellow to black. For the samples prepared with a double anti-solvent dripping, the second anti-solvent dripping (80 \\u03bcl) was applied after 80 s and the spinning time was prolonged to 120 s. The perovskite films were then heated either from room temperature to 70 \\u00b0C or directly placed on a 70 \\u00b0C hot plate for 20 minutes. The solution for coating the electron transport layer \\u2013 PC60BM (20 mg ml\\u22121 in CB) \\u2013 was stirred overnight at room temperature under inert conditions and filtered through a 0.45 \\u03bcm PTFE filter before use. The solution was spin coated onto the absorber layer at 6000 rpm for 60 s. Afterwards, the top electrode (100 nm Al) was deposited by thermal evaporation under high vacuum conditions (<1 \\u00d7 10\\u22125 mbar) using a shadow mask (electrode area: 0.09 cm2).\\n\\nThe MA0.75FA0.15PEA0.1SnI3 perovskite thin film was characterized by X-ray diffraction (XRD) with a PANalytical Empyrean system, which uses Cu K\\u03b1 radiation. UV-Vis measurements of the perovskites were performed using a Perkin Elmer Lambda 35 UV/VIS spectrometer equipped with an integrating sphere. The optical data were recorded in the wavelength range of 300 to 1100 nm. Top view SEM images of the MA0.75FA0.15PEA0.1SnI3 perovskite thin films on glass/ITO/PEDOT:PSS were acquired on a Zeiss Supra 40 scanning electron microscope with an in-lens detector and 5 kV acceleration voltage.\\nJV curves of all devices were recorded inside a glove box (nitrogen atmosphere) with a scan rate of 110 mV s\\u22121 using a Keithley 2400 source meter connected to a LabView-based software. The solar cells were illuminated through a shadow mask (2.65 \\u00d7 2.65 mm2) and the illumination (100 mW cm\\u22122) was provided by a Dedolight DLH400 lamp, calibrated using a monocrystalline silicon WPVS reference solar cell from Fraunhofer ISE. For the illumination during the stability tests as well as for the light intensity dependent measurements of JSC and VOC, a white light (6500 K) 10 W chip-on-board high power LED was used. External quantum efficiency (EQE) measurements were acquired in inert atmosphere using a MuLTImode 4-AT monochromator (Amko) equipped with a 75 W xenon lamp (LPS 210-U, Amko), a lock-in amplifier (Stanford Research Systems, Model SR830), and a Keithley 2400 source meter. The monochromatic light was chopped at a frequency of 30 Hz and constant background illumination was provided by white light LEDs. The EQE spectra were measured in the wavelength range of 380\\u20131050 nm (increment: 10 nm). The measurement setup was spectrally calibrated with a silicon photodiode (Newport Corporation, 818-UV/DB).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: (PEA)0.1FA0.15MA0.75SnI3,\\n Perovskite_composition_short_form: (PEA)FAMASnI,\\n Perovskite_additives_compounds: SnF2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 70,\\n Stability_PCE_initial_value: 3.5,\\n Stability_PCE_end_of_experiment: 120,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless otherwise stated, all materials were purchased from Sigma-Aldrich and used without further purification. Formamidinium iodide (FAI, CH(NH2)2I), Methylammonium bromide (MABr, CH3NH3Br), PCBM (phenyl\\u2013C61\\u2013butyric acid methyl ester, >99%), and PEDOT:PSS dispersion were purchased from Lumtec. PbI2 (99.9985%) was obtained from Alfa Aesar. Hydrochloric acid (HCl, 35\\u201337%), chloroform (CHCl3, 98%), and ammonia solution (NH4OH) were purchased from Samchun Chemical (Korea).\\n\\nPANI powder was synthesized using a self-stabilized dispersion polymerization (SSDP) method to reduce undesirable side reactions; with this method, chemical oxidative polymerization occurs at the aqueous medium/organic solvent interface at low temperatures. 2 g of aniline monomer was added to 40 mL of 1.2 M HCl aqueous solution. Then, 60 mL of chloroform was poured into the aqueous anilinium ion solution to induce interfacial polymerization of aniline monomers. Oxidizing agent was prepared by dissolving 2.4 g of ammonium persulfate in 15 mL of 2 M HCl aqueous solution. The resulting oxidizing agent was added into the reaction medium to initiate polymerization. The polymerization of aniline proceeded with vigorous stirring for 16 h at \\u221240 \\u00b0C. After washing with water, ethanol, and acetone, precipitates of greenish PANI ES powder were obtained. The PANI ES power was dispersed in 200 mL of 0.6 M NH4OH aqueous solution and stirred for 12 h to fully reduce. The products were washed with water, ethanol, and acetone to produce brownish PANI EB powder. Secondary doping of the PANI EB powder was conducted by grinding with CSA (the mole ratio of CSA to aniline = 1:2) using a mortar. CSA-doped PANI powders were dispersed in m-cresol/chloroform (7:3, v/v) co-solvent to a concentration of 3 mg mL\\u22121. The PANI-CSA dispersion was vigorously stirred and sonochemically treated for 24 h to obtain homogenous dispersion. The PANI-CSA remained well-dispersed in m-cresol/chloroform for months without agitation. Before use, the dispersion was diluted to 0.5 mg mL\\u22121 by adding chloroform.\\n\\nThe PSCs were fabricated on patterned, FTO-coated glass with a sheet resistance of 15 \\u03a9 sq\\u22121. FTO substrates were cleaned sequentially in deionized water, acetone, and 2-propanol for 30 min using an ultra-sonication bath. HTLs were deposited by spin-coating PEDOT:PSS and PANI-CSA dispersions at 5000 rpm and annealing at 120 \\u00b0C for 20 min. The mixed perovskite (Cs0.05MA0.16FA0.79Pb(I0.84Br0.16)3) precursor solution was prepared by dissolving FAI (1M), PbI2 (1.1 M), PbBr2 (0.2 M), MABr (0.2 M), and CsI (0.06 M) in dimethylformamide:dimethyl sulfoxide (DMF:DMSO; 4:1, v-v) co-solvent, with stirring at 60 \\u00b0C. The perovskite precursor solution was dropped onto the pre-heated substrate at 40 \\u00b0C, and spin-coated at 1000 rpm for 10 s and 5000 rpm for 23 s. After \\u223c15 s of second spin-coating step, 0.3 mL of chlorobenzene was dripped onto the center of the substrate to induce fast crystallization of the perovskite film. After the whole spin-coating process, the substrate was annealed at 100 \\u00b0C for 20 min. PCBM solution (20 mg mL\\u22121 in chlorobenzene) with Triton X-100 (3 wt% of PCBM) was prepared as described in our previous report and deposited via spin-coating at 2500 rpm for 40 s. Finally, a 65 nm-thick Au top electrode was deposited by thermal evaporation for better ambient stability. All solar cell fabrication procedures were carried out in ambient air (temperature = 23 \\u00b0C, relative humidity <30%).\\nFor the flexible PSCs, PET/ITO substrates were mounted on glass during the fabrication; the fabrication procedures were the same as those described above for the rigid devices.\\n\\nThe FE-SEM images were obtained from JSM-7800F Prime microscopes (JEOL, Japan), installed at the National Center for Inter-university Research Facilities (NCIRF), Seoul National University. The transmittance of the conducting polymer films and ultraviolet-visible (UV-vis) absorption spectra of the perovskite films were measured with a Lambda 35 double beam UV-vis spectrophotometer (Perkin-Elmer, USA). The UPS spectra were measured by Axis Supra (Kratos, UK) with a minimum step size of 1 meV and sensitivity of 1000000 cps at 120 meV resolution. XRD of the perovskite films was measured using SmartLab (Rigaku, Japan). The J\\u2013V characteristics of the PSCs were measured using an I\\u2013V tracer (MP-160; Eko Instruments, Japan) under standard AM 1.5 G (100 mW cm\\u22122) illumination from a 500 W xenon lamp, calibrated with a KG5-filtered Si reference cell (K801; McScience Inc., Korea). Steady-state photocurrent output and electrochemical impedance spectra (EIS) of the PSCs, and J\\u2013V plots of the hole-only devices were measured by the Zive Lab equipment (WonATech, Korea). The Mott-Gurney law equation (J = (9/8)\\u03bc\\u03b50\\u03b5(V2/d3)) was used to determine the charge mobility, where \\u03bc, \\u03b50, \\u03b5, and d are the charge mobility, free space permittivity, relative dielectric constant, and film thickness, respectively. The relative dielectric constant for both PEDOT:PSS and PANI-CSA is assumed to be 3, which is a typical value for conjugated polymers. The TrPL were measured under exposure to a 520 nm pulse laser (PicoQuant, Germany).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Triton X-100,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.48I2.52,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: Unknown,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 240,\\n Stability_PCE_initial_value: 13.7,\\n Stability_PCE_end_of_experiment: 32,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I (MAI, 99.999%), PbI2 (99.999%), MACl (99.999%) and DMF (99.8%) were purchased from the Yingkou You Xuan Trade CO., LTD. All the remaining chemical medicine and reagents were purchased from Sigma-Aldrich. The standard precursor solution was prepared in a glovebox by dissolving the MAI (190.8 mg) and PbI2 (553.2 mg) in DMF (1 mL). As for MACl coordination with a heat assisted process (MACl\\u2013HAP), MACl (40.5 mg) was added to the standard precursor solution. The precursor solution was stirred for 1\\u20132 h and aged for 12 h before spin coating. The FTO substrates were ultrasonically cleaned with deionized water, ethanol, and acetone successively. The as-cleaned substrates were heated in an oven at 60 \\u00b0C for 1 h followed by the UV\\u2013ozone treatment for 10 min. The TiO2 electron transport layer was deposited on the FTO substrate at 450 \\u00b0C by a spray pyrolysis method. For MACl\\u2013HAP, the substrates were heated for 10 min at the different temperatures (70, 90 and 110 \\u00b0C). Then, the perovskite precursor solution (45 \\u03bcL) was spin coated onto the FTO substrates at 6000 rpm for 30 s, followed by annealing at 100 \\u00b0C for 30 min to promote the crystal growth and eliminate the by-product. As for ASP, the anti-solvent was added at 6 s during the spin-coating process. The hole transfer layer was spin-coated using chlorobenzene solution containing Spiro-MeOTAD (72.3 mg mL\\u22121), tertbutyl pyridine (28.8 \\u03bcL mL\\u22121) and li-TFSI solution (17.5 \\u03bcL mL\\u22121) at 4000 rpm for 30 s. Finally, an Au counter electrode was formed by thermal evaporation. The active area was 0.1057 cm2.\\n\\nA cold field emission scanning electron microscope (SU8020, Hitachi) was used to characterize the morphology of the MAPbI3 film. The process of crystal growth and transformation was analyzed by an X-ray diffractometer (PANalytical, the Netherlands) with a monochromatic Cu K\\u03b1 radiation source (\\u03bb = 1.54056 \\u00c5) and an ultraviolet-visible (UV-vis) spectrophotometer (UV-3600, Shimadzu).\\n\\nThe space charge limited current (SCLC) was obtained by a 2400 Source Meter in a dark environment, under bias from 0.008 V to 2 V. The electrochemical impedance spectroscopy (EIS) of the devices was performed using an electrochemical workstation (Zahner, Zennium). The J\\u2013V curves and stabilized Jsc were recorded using a digital source meter (2400, Keithley Instruments Inc.) under 3A grade AM 1.5G simulated sunlight (100 mW cm\\u22122) (7-SS1503A, 7 Star Optical Instruments Co., Beijing, China). The incident light intensity was calibrated with an NREL-calibrated Si solar cell (Newport, Stratford Inc., 91150 V). The scan rate was 50 mV s\\u22121 and delay time was 0.1 s. The reverse scan was from 1.2 V to \\u22120.05 V, while the forward scan was from \\u22120.05 V to 1.2 V. The incident photon conversion efficiency (IPCE) was measured by the direct current (DC) mode using a custom measurement system consisting of a 150 W Xenon lamp (7ILX150A, 7 Star Optical Instruments Co., Beijing, China), a monochromator (7ISW30, 7 Star Optical Instruments Co., Beijing, China) and a digital source meter (2400, Keithley Instruments Inc.). These characterizations of the PSCs without encapsulation were carried out under ambient air conditions.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 216,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 0.1057,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO glass with a sheet resistance of 15 \\u03a9 \\u25a1\\u22121 was cleaned with a chemical detergent, facilitated by ultrasonication, with water, acetone and iso-propanol successively prior to PEALD of SnO2. An ITO/PET (45 \\u03a9 \\u25a1\\u22121) substrate was cleaned by the same procedure. Tetrakis(dimethylamino)-tin(IV) (99%, TDMA-Sn, Strem Chemicals Inc.) was used as the Sn precursor and pure O2 (ultra-high pure, Airgas) was used as the oxidizer. Ar (ultra-high pure, Airgas) was used as the carrier gas with a flow rate of 15 sccm. PEALD SnO2 was deposited at 100 \\u00b0C with an Ensure Scientific Group AutoALD-PE V2.0 equipped with a plasma generator. The TDMA-Sn precursor was held at 75 \\u00b0C. The resulting deposition rate is about 1.7 \\u00c5 per cycle as determined by spectroscopic ellipsometry.\\n\\nA 45% by weight precursor solution was prepared with lead iodide (PbI2, Alfa Aesar, 99.9985%) and methylammonium iodide (MAI) (molar ratio = 1:1) in N,N-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) (volume ratio = 9:1). A small amount of lead thiocyanate (Pb(SCN)2, Sigma-Aldrich, 99.5%) was added into the precursor solution as an additive. It has been shown that the Pb(SCN)2 additive can enlarge the grain size of the resulting perovskite thin films and subsequently improve the cell performance. The solution was stirred for 12 hours on a 60 \\u00b0C hot plate before deposition.\\n\\nThe C60-SAM was purchased and used without further purification. The C60-SAM at a concentration of 4 mg mL\\u22121 was dissolved in chlorobenzene (Sigma-Aldrich, 99.8%) under vigorous stirring overnight. The C60-SAM was then deposited onto the SnO2 ESL by a spin coating method as previously reported. The perovskite precursor solution was spin-coated on the C60-SAM/SnO2 ESLs first at 500 rpm for 3 s and then at 4000 rpm for 60 s using an anti-solvent technique. Diethyl ether, as the anti-solvent agent, was then drop-cast on the substrate. After spin coating, the perovskite film was annealed at 65 \\u00b0C for 2 minutes and then at 100 \\u00b0C for 5 minutes. All of these processes were carried out in a N2 filled glove box. Spiro-OMeTAD (Shenzhen Feiming Science and Technology Co., Ltd., 99.0%) was used as the HSL and deposited on the perovskite film at 2000 rpm for 60 seconds. The Spiro-OMeTAD solution was prepared by dissolving 72.3 mg Spiro-OMeTAD in 1 mL chlorobenzene with 28 \\u03bcL 4-tert-butylpyridine (TBP) (Sigma-Aldrich, 96%) and 18 \\u03bcL Li-bis(trifluoromethanesulfonyl)imide (Li-TFSI) (Sigma-Aldrich, 99.95%) (520 mg mL\\u22121 in acetonitrile). A layer of 80 nm gold (Au) was then deposited on the top of Spiro-OMeTAD using thermal evaporation. The working area of the devices was 0.08 cm2 as defined by a shadow mask during the Au evaporation.\\n\\nCurrent density\\u2013voltage (J\\u2013V) curves were obtained under standard AM 1.5 G illumination using a solar simulator (PV Measurements, Inc) equipped with a 450 W xenon lamp with an output intensity of 100 mW cm\\u22122 calibrated with a reference Si cell at the measurement location. The light intensity was later adjusted between 0.5 and 100 mW cm\\u22122 using neutral density filters. EQE measurements were carried out with an EQE system (PV Measurements, Inc) using 100 Hz chopped monochromatic light ranging from 300 nm to 900 nm under otherwise near-dark test conditions. Transmission spectra and ultraviolet-visible absorbance spectra were measured with an ultraviolet-visible spectrophotometer (CARY5000, Varian, Australia). Impedance spectra were recorded on an electrochemical workstation (Voltalab PGZ-301) at 0 mV bias in the dark. The plane view and cross sectional structures of the substrates and PVSCs were characterized with a field emission SEM instrument (Hitachi S-4800). The crystallinity and the crystal structure of the perovskite layer were analyzed with an Ultima III X-ray diffractometer using a Ni-filtered Cu K\\u03b1 X-ray source (Rigaku Corp.). The film thickness was analyzed via spectroscopic ellipsometry using a single rotating compensator multichannel ellipsometer (Model M2000FI, J. A. Woollam Co., Inc.). AFM was carried out with a Nanoscope V atomic force microscope operating in the tapping-mode (Veeco Metrology Group). The sheet resistance was measured using a four-point probe method resistivity test system (PRO4-440N, Lucas labs).\\n\\nPL and TRPL measurements were performed at room temperature in ambient air. The samples were excited through the glass side (i.e. ESL side). For steady-state PL, a 532 nm cw laser (intensity = 11 mW cm\\u22122, beam diameter \\u2248 140 \\u03bcm) was used as a source of excitation. The PL signal was detected with a Symphony-II CCD (from Horiba) detector after a 300 g mm\\u22121 grating monochromator (integration time = 0.5 s). Time resolved photoluminescence measurements were performed using a time correlated single photon counting module (Becker & Hickel Simple Tau SPCM 130-E/M module). A 532 nm pulsed laser (0.2 mW cm\\u22122, beam diameter \\u2248 100 \\u03bcm) was used as a source of excitation. The photoluminescence signal was dispersed with a Horiba IHR 320 monochromator (grating 900 g mm\\u22121, 850 nm blaze, and detected with a hybrid APD/PMT module (Hamamatsu R10467U-50)). TRPL measurements were performed (integration time = 1200 s) at a 1 MHz repetition rate. TCSPC decay curves obtained in the TRPL measurements were fit to two-exponential decay by iterative re-convolution with the measured system response function (W). The mean photogenerated carrier life time is calculated by the weighted average as follows:\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c | C60-SAM,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: ALD | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Pb(SCN)2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65; 100,\\n Perovskite_deposition_thermal_annealing_time: 2.0; 5.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 480,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 100,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals and solvents were used as received unless stated otherwise. The grooved roller is commercially available. The SnO2 colloid precursor was obtained from Alfa Aesar (tin(IV)oxide). The perovskite precursor solution contained a mixture of MAI and PbI2 (1:1, molecular ratio) in anhydrous DMF:DMSO 9:1 (v/v). Methylammonium acetate (MAAc) was synthesized according to the reported literature with a slight modification. Briefly, 50 ml of ethanol, 5 ml of acetate (99.5%, Aladdin Reagents), and 12 ml of methylamine (30\\u201333 wt% in ethanol, Aladdin Reagents) were added sequentially in a 250 ml round-bottom flask. The solution was stirred at room temperature for 2 h and then put into a vacuum chamber with a solid desiccant (silica gel). The chamber pressure was maintained at 0.1 MPa for 24 h. The resultant colorless and viscous liquid was stored in a nitrogen-filled glovebox for further use.\\n\\nFTO glass was cleaned sequentially in detergent, acetone, isopropanol and deionized water before using. The FTO was cleaned by UVO for 15 min. Then, the SnO2 nanoparticle film (7.5%), as an ETL, was spin-coated at 4000 rpm for 30 s, or roller-coated at a speed of 10\\u201350 mm s\\u22121 using a roller with a groove depth of 6 \\u03bcm, and annealed in ambient air at 150 \\u00b0C for 30 min. After that, 50 \\u03bcl of a 1.3 M MAPbI3 precursor solution with an additive (10\\u201315% MAAc, volume ratio) was spin-coated at 1000 rpm for 10 s and then 3000 rpm for 70 s onto SnO2 surface, followed by annealing at 100 \\u00b0C for 5 min. Meanwhile, MAPbI3 precursor solution of a different concentration, with the additive (10\\u201315% MAAc, volume ratio), was dropped onto SnO2 surface and instantly roller-coated at a speed of 10\\u201350 mm s\\u22121 using a roller with groove depths of 2 \\u03bcm, 6 \\u03bcm and 10 \\u03bcm, followed by annealing at 100 \\u00b0C for 5 min. During this coating process the SnO2 substrate was heated to 40 \\u00b0C. The hole transporting layer (HTL) solution was prepared by dissolving spiro-OMeTAD (80 mg), tBP (28.5 \\u03bcl) and a Li-TFSI (35 \\u03bcl) solution (260 mg Li-TFSI in 1 ml acetonitrile) in 1 ml chlorobenzene and spin casted on the perovskite film at 6000 rpm for 30 s, or roller-coated at a speed of 10\\u201350 mm s\\u22121 on top of the perovskite absorbing layer film. Then, an Au counter electrode was deposited by thermal evaporation using a shadow mask. Otherwise, N2 gas flow was also introduced to the dry wet-films acceleratedly in all roller-coating processes.\\n\\nThe absorption spectra were measured with a UV-Vis-NIR spectrophotometer (Cary 5000) in the wavelength range of 300 to 1200 nm at room temperature. The morphology of the perovskite films was characterized using a scanning electron microscope (SEM, JEOL JSM-6700F). A solar simulator (HAL-320, Asahi Spectra Co. Ltd., Japan) with a compact xenon light source was used to produce the simulated AM 1.5G irradiation (100 mW cm\\u22122), and the calibration of the light was carried out by a detector (CS-20, Asahi Spectra Co. Ltd., Japan) with a silicon reference cell. Photocurrent density\\u2013voltage (J\\u2013V) curves of the solar cells were measured at 25 \\u00b0C. The scanning step was 40 mV for the J\\u2013V curve measurement. Unless specified, a bias scan from 1.2 V to \\u22120.2 V was run first (reverse scan) followed by a return back (forward scan) with a delay time of 50 ms. A metal mask with a window of 0.1 cm2 was covered on the light illumination side to define the active area of the cell. The spectral response was measured by an external quantum efficiency (EQE) measurement system (QEX10, PV Measurement) with a scanning step of 10 nm. A xenon arc lamp was used as the monochromatic light excitation source and filtered by a double grating. Photoluminescence (PL) and time-resolved photoluminescence (TRPL) measurements were performed by a spectrometer (Edinburgh FS5) at room temperature with a laser wavelength of 532 nm and power of 0.2 mW respectively. X-ray diffraction (XRD) patterns were studied on a Rigaku ATX-XRD with Cu K\\u03b1 radiation (k = 1.5405 \\u00c5).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: MAAc,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Roller-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 500,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 87,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were commercially available and used as purchased, including PbI2 (99%, Sigma-Aldrich), HC(NH2)2I, CH3NH3Cl (>98%, Tokyo Chemical Industry Co., Japan), nickel acetylacetonate (95%, Sigma-Aldrich), PC61BM (99.5%, Lumtec Co., Taiwan). Magnesium acetate tetrahydrate (99%), lithium acetate (99%) and super dehydrated solvents of dimethylsulfoxide (DMSO), toluene, chlorobenzene, acetonitrile, methanol, and ethanol were all purchased from Wako Co., Japan.\\n\\nDevices with an FTO/NiOx/FAPbI3/PCBM/TiOx/Ag structure were prepared as follows: FTO glasses were put in detergent, deionized water, ethanol and acetone successively, and thoroughly washed using ultrasonic cleaners. The cleaned FTO glasses were placed on a hotplate at a temperature of 500 \\u00b0C. To deposit the NiOx layer, 30 ml of an acetonitrile/ethanol (with 95:5 volume ratio) solution of nickel acetylacetonate (with 15 mol% magnesium acetate tetrahydrate and 5 mol% lithium acetate, totally 0.02 mol l\\u22121) was sprayed, and an NiOx layer with a thickness of approximately 30 nm was obtained. Doping of 5 mol% Li+ into the NiO film was performed to increase the p-conductivity, and doping of 15 mol% Mg+ into the NiO film was performed to adjust the valence band (EVB). The optimization of the NiOx layer with Li+ and Mg+ doping can be found in previous work. After spraying, the film was further annealed at 500 \\u00b0C for 15 min to promote NiO crystallization. After cooling, the NiO-coated FTO glasses were transferred to the N2-filled glove box.\\nThe method for perovskite layer deposition was modified from a previous report: first, an 80 \\u03bcl 1.2 M DMSO/DMF (1:5) solution of PbI2/FAI (1:1) mixture was spread onto FTO glass; then, the spin-coater was started at a rotation speed of 1000 rpm for 10 s and 5000 rpm for another 30 s. 100 \\u03bcl chlorobenzene (CB) was drop-cast quickly at 10 s after the 5000 rpm spin-coating started. Then 20 \\u03bcl of different concentrations of MACl solution (0, 1, 5 and 10 mg ml\\u22121, isopropanol) were spin-cast on the top of the film at 5000 rpm. The perovskite films were formed by heating at 100 \\u00b0C for 10 min and further annealing at 140 \\u00b0C for 20 min. After cooling, the PCBM solution (20 mg ml\\u22121 dissolved in CB) was spin-coated on top of the perovskite film at a rotation speed of 1000 rpm for 30 s. Then, 100 \\u03bcl TiOx precursor solution, containing titanium isopropoxide (with 5 mol% niobium ethoxide, diluted in methanol with a volume ratio of 1:500), was drop-cast onto the surface of the PCBM layer at 6000 rpm. The film was then dried at 70 \\u00b0C for 10 min on a hot plate. To promote hydrolysis of the deposited titanium isopropoxide and to form the TiOx layer, 150 \\u03bcl of the H2O/methanol (1:99) mixed solution was drop-cast slowly at 6000 rpm for 30 s. Subsequently, an Ag film with a thickness of 100 nm was deposited under high vacuum (<3 \\u00d7 10\\u22124 Pa) in the evaporator chamber. To seal the solar cells, the edge of cavity glass was smeared with UV glue, and covered on the top of the FTO glass with active films in-between. The UV glue was solidified by exposure to 300 W UV light for 15 s. The sealing process was performed in a glove box. All the J\\u2013V parameters were obtained using these sealed devices.\\n\\nCurrent\\u2013voltage characteristics were measured with voltage step of 10 mV and a delay time of 50 ms using a black metal mask with an aperture area of 0.25 cm2 under standard air mass 1.5 sunlight (100 mW cm\\u22122, WXS-155S-10: Wacom Denso Co., Japan). Monochromatic incident photon-to-current conversion efficiency (IPCE) spectra were measured with a monochromatic incident light of 1 \\u00d7 1016 photons cm\\u22122 in direct current mode (CEP-2000BX, Bunko-Keiki). SEM images (top-view SEM and cross-sectional SEM) were obtained using a JSM-6500F field-emission SEM. The XRD pattern was measured using a Rigaku MiniFlex X-ray diffractometer with Cu K\\u03b1 radiation. The UV-vis spectra were measured on a Shimadzu UV/Vis 3600 spectrophotometer with an integrating sphere. The steady-state photoluminescence spectrum and quantum efficiency were measured by absolute quantum yield measurement system equipped with a 532 nm continuous wave (CW) laser excitation source, an integrating sphere and fiber-coupled detector (Ocean Optics MayaPro). Time-resolved photoluminescence decay was acquired using a time-correlated single photon counting setup, excited by a 405 nm pulse laser with an excitation energy of 100 \\u03bcW and repetition rate of 5 MHz. The XPS were performed in a Kratos Ultra Spectrometer (AXIS-ULTRA DLD-600 W) using monochromatized Al K\\u03b1 X-ray photons (hv = 1486.6 eV for XPS) and an HeI (21.2 eV for UPS) discharge lamp. The light-soaking stability was tested in a solar-cell light-resistance test system (Model BIR \\u2013 50, Bunkoh-Keiki Co., LTD), which was equipped with a Class AAA solar simulator; <420 nm UV light was cut off with an optical filter. Thermal stability was tested under controlled temperature at 85 \\u00b0C in an electronic constant temperature/humidity chamber (THR030FA, Advantec Co., Ltd).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FAMAPbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: NiMgLiO,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spray-pyrolys,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 500,\\n Stability_PCE_initial_value: 20.65,\\n Stability_PCE_end_of_experiment: 85,\\n Cell_area_measured: 0.25,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped tin oxide (FTO)-coated glass (TEC-15, NSG-Pilkington) substrates were first ultrasonically cleaned with cleaning fluid, deionized water, alcohol, and acetone, respectively, for 20 minutes in sequence. After drying with a stream of nitrogen, the NiMgLiO-based hole extraction layer was then deposited onto FTO-glass by spray pyrolysis at 570 \\u00b0C. The precursor solution was composed of nickel(II) acetylacetonate in a super-dehydrated acetonitrile and ethanol mixture. After cooling, the NiMgLiO-coated FTO glasses were transferred quickly to a N2 filled glovebox. Then, anti-solvent assisted spin-coating technology was used for the MAPbI3(CaI2)x perovskite film (450 nm) deposition. Typically, a 1.5 M DMF/DMSO (4:1 by volume ratio) solution mixture of PbI2/MAI/CaI2 (1:1:x by molar ratio, x = 0, 0.002, 0.005, 0.01, 0.02) was spin-coated at 6000 rpm for 30 seconds, followed by the diethyl ether (800 \\u03bcl) drip during spinning. This was followed by the deposition of a thin PCBM layer (60 nm) by spin-coating its chlorobenzol solution (20 mg mL\\u22121) at 1600 rpm for 30 seconds. Subsequently, a BCP layer (5 nm), used as the buffer layer, was thermally evaporated under high vacuum (<5 \\u00d7 10\\u22124 Pa). Finally, the device was completed by thermal evaporation of a 100 nm-thick Ag electrode.\\n\\nTop-view scanning electron microscope (SEM) images were taken on a high-resolution SEM (Hitachi-4800) at a 10 kV accelerating voltage. X-ray photoelectron spectroscopy (XPS) measurements were carried out on a Kratos Ultra spectrometer (AXIS-ULTRA DLD-600W). The surface morphologies of the perovskite films were examined by using an atomic force microscope (AFM: Shimadzu, SPM-9700). The crystal structures of the perovskite films were characterized using a Philips X-ray diffractometer with Cu K\\u03b1 radiation. The UV-vis spectra were obtained from a Shimadzu UV/vis 3600 spectrophotometer with an integrating sphere. Steady-state PL spectra were obtained from a Horiba Jobin Yvon system with an excitation laser beam at 532 nm. Transient PL spectra were recorded with time-correlated single photo counting system (PicoHarp 300, PicoQuant GmbH). The photocurrent density-voltage (J\\u2013V) curves were recorded using a Keithley 2400 source meter. A solar simulator (Oriel) fitted with a filtered 450 W xenon lamp was used to provide solar simulated radiation. The light intensity of the simulated sunlight was calibrated to be 100 mW cm\\u22122 by using a standard c-Si solar cell and the effective area of the solar cell was defined to be 0.09 cm2 using a non-reflective metal mask. The IPCE measurements were carried out with a Newport IPCE system (Newport, USA). The Mott\\u2013Schottky plots were recorded on an electrochemical workstation (Zahner Zennium, Germany).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: CaI2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: NiMgLiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spray-pyrolys,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 300,\\n Stability_PCE_initial_value: 17,\\n Stability_PCE_end_of_experiment: 93,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials were purchased from Sigma-Aldrich and used as received without further purification unless otherwise stated. MAPbI3 perovskite precursor solution was prepared in an argon-filled glovebox by dissolving 461 mg of PbI2, 159 mg of methylammonium iodide (MAI) (Dyesol), and 78 mg of dimethyl sulfoxide (DMSO) in 700 mg of dimethyl formamide (DMF) at room temperature, under rigorous stirring for one hour. Mixed halide perovskite MAPbI3\\u2013PbCl2 additive precursor solution was prepared by adding different amounts of PbCl2 (1%, 2.5%, 5%, 7.5%, and 10% (molar ratio with respect to PbI2)) to the prepared MAPbI3 perovskite precursor. The solution was then magnetically stirred for an additional hour. The prepared perovskite solution was filtered by using a syringe filter (pore size: 0.22 \\u03bcm) prior to use for deposition of the film. A solution for the hole transporting material was prepared by addition of 72.3 mg of 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene (Spiro-MeOTAD) (Borun New Material), 28.8 \\u03bcL of 4-tert-butylpyridine, and 17.5 \\u03bcL of bis(trifluoromethane)sulfonimide lithium (Li-TFSI) solution (520 mg of Li-TFSI in acetonitrile) into 1 mL of chlorobenzene.\\n\\nSolar cells were fabricated using fluorine-doped tin oxide (FTO) coated glass (Nippon Electric Glass, 15 \\u03a9 \\u25a1\\u22121) as the substrate which was firstly patterned through partial removal of FTO via etching using 35.5 wt% HCl and zinc powder. The substrates were then cleaned in sequence in 5% Decon-90 detergent, and a mixture of acetone, isopropanol and ethanol for 20 min each in an ultrasonic bath. Prior to use, the substrates were treated with ultraviolet ozone for 30 min to fully remove organic solvent residuals. An electron transporting layer based on the TiO2 film (\\u223c40 nm) was deposited in air via spin-coating a 0.15 M solution of titanium diisopropoxide bis(acetylacetonate) in 1-butanol at 2000 rpm for 20 s. The film was then dried at 125 \\u00b0C for 5 min and annealed at 450 \\u00b0C for 30 min. A mesoporous TiO2 (mp-TiO2) layer (\\u223c200 nm) was spin-coated onto the compact TiO2 film using a diluted TiO2 paste (0.12 g TiO2 paste (Dyesol) in 1 mL of absolute ethanol) at 2000 rpm for 20 s, followed by sintering at 450 \\u00b0C for 30 min. After cooling to room temperature, the film was treated with 20 mM TiCl4 aqueous solution at 90 \\u00b0C for 10 min. The TiCl4-treated film was cleaned with distilled water and annealed again at 450 \\u00b0C for 30 min. After this, the TiO2 coated film was treated in a UV-zone for 20 min before being transferred to an Ar-filled glovebox. Perovskite layers (\\u223c400 nm) with and without PbCl2 in the perovskite precursor solution were deposited onto the prepared TiO2 layer at 4000 rpm for 20 s. During spin-coating, 0.5 mL of diethyl ether was dropped on the center of the spinning substrate before it turned turbid. The perovskite layer was then dried at 65 \\u00b0C for 1 min, and annealed at 100 \\u00b0C for 2 min. The hole-transport layer (\\u223c200 nm) was deposited from the prepared Spiro-OMeTAD solution onto the as-prepared perovskite layer at 4000 rpm for 25 s. The device fabrication was finished by deposition of a 100 nm layer of gold film for back contact on the prepared sample via an e-beam evaporation process under 10\\u22126 torr pressure.\\n\\nThe top-view and cross-sectional scanning electron microscopy (SEM) images of the samples were taken using a field emission scanning electron microscope (FSEM JOEL 7001F) at an acceleration voltage of 5 kV. The UV-vis absorbance spectrum was measured with a UV-visible spectrometer (Cary 50). The crystal structure of the perovskite film as-deposited on FTO/compact TiO2/mp-TiO2 was determined by X-ray diffraction (Rigaku SmartLab) with monochromatic CuK\\u03b1 (\\u03bb = 0.154 nm) as an excitation source. A scan rate of 1.5\\u00b0 per minute and a step size of 0.015\\u00b0 were used in the XRD measurement. The performance of perovskite devices was measured under irradiation of 100 mW cm\\u22122 (AM1.5) provided by a solar simulator (Oriel Sol3A, Newport) equipped with a 450 W Xenon lamp. IPCE measurement was conducted by using a quantum efficiency system (IQE 200B, Newport) in AC mode. Electrochemical impedance spectroscopy (EIS) of the PSCs was performed in a frequency range from 1 MHz to 100 mHz using an electrochemical workstation (VSP BioLogic Science Instruments) at a forward bias of 0.5 V in darkness. An AC voltage with a perturbation amplitude of 10 mV was applied in the EIS measurement. X-ray photoelectron spectroscopy (XPS) (Kratos Axis Ultra) using mono Al K\\u03b1 (1486.6 eV) X-rays was used to detect the elements in the perovskite film. For XPS depth profiling, a 4 keV Ar+ ion was used for the charge-up effect. The photoluminescence (PL) spectrum was measured with a fluorescence spectrometer (Edinburgh Instruments Ltd) at room temperature. The film was photo-excited by using a laser (474 nm) with a pulse wavelength of 82.4 ps. Scanning Kelvin Probe Force Microscopy (KPFM) (Oxford instrument, Asylum Research) was performed on the prepared perovskite film under ambient conditions using a NSG-03 Pt coated cantilever at room temperature. The work function of the cantilever was measured using a HOPG standard sample. The chloride analysis was performed on a Dionex RFIC ICS-2100 Ion Chromatography (IC) system (Thermo Scientific) with an ASDV auto sampler system. A Dionex-IonPac AS18 4 mm and a Dionex EGC-KOH II Cartridge were used as the column and eluent, respectively. The suppressor (ASRS 300, 4 mm) operated at 82 mA. The calibration standards were diluted from an IC standard (containing 1000 \\u03bcg mL\\u22121 of Cl) purchased from Choice Analytical. Perovskite/FTO samples (2 \\u00d7 1.5 cm) were immersed into 2 mL of Milli-Q water in a clean beaker until the perovskite layer was fully removed. The amount of dissolved perovskite material in water was used for further calculation. 1.2 mL of the resulting solution was pipetted out and further diluted five fold for IC measurements.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1.3,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 65,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Bismuth iodide (BiI3, 99%), lead iodide (PbI2, 99.9%), dimethyl sulphoxide (DMSO, anhydrous, 99.8%) and N,N-dimethylformamide (DMF, anhydrous, 99.8%) were purchased from Sigma-Aldrich. Formamidinium iodide (FAI, 99.9%) was purchased from Xi'an Polymer Light Technology Corp. All salts and solvents were used as received without any further purification.\\n\\nThe controlled \\u03b1-FAPbI3 perovskite precursor solution was prepared by fully dissolving 0.01 mol FAI and 0.01 mol PbI2 in 10 mL solvent obtained by mixing DMSO and DMF (3:7, v/v). Bi3+-incorporated FAPbI3 perovskite precursor solutions were prepared by fully dissolving 0.01 mol FAI and 0.01 mol mixture of PbI2/BiI3 (molar ratios of BiI3 in the mixture ranged from 5 to 50 mol%) in 10 mL solvent obtained by mixing DMSO and DMF (3:7, v/v). Then, the precursor solutions were stirred at 70 \\u00b0C for 12 h.\\n\\nFirst, a fluorine-doped tin oxide (FTO) conducting glass (sheet resistance of 8 ohm per square) was ultrasonically cleaned by detergent, deionized water, and acetone for 20 min sequentially, and then treated with a UV/O3 cleaner for 15 min. Then, a uniform dense TiO2 layer was deposited on the FTO glass substrate by spin coating 0.15 mol L\\u22121 titanium diisopropoxide bis(acetylacetonate) in butanol at 3500 rpm and repeating the process twice, and then sintering at 500 \\u00b0C for 30 min. Subsequently, the perovskite film was deposited on the compact TiO2 layer by two-step spin coating of the as-prepared precursor solution at 800 rpm for 10 s and 3500 rpm for 25 s. During the second step, diethyl ether was dripped on the rotating film 15 s before the end of the process. The spin-coated film was annealed at 180 \\u00b0C for 15 min to form the perovskite film. Afterward, the final film was covered by the hole transporter spiro-MeOTAD. 0.167 g spiro-MeOTAD was dissolved in 1.00 mL chlorobenzene, and 0.0103 g LiTFSI and 0.0298 g tert-butylpyridine (TBP) were used as additives and then the solution was deposited by spin-coating at 5500 rpm for 30 s. Finally, a 100 nm-thick Au electrode was deposited on top of the device through a shadow mask by thermal evaporation under ca. 5 \\u00d7 10\\u22125 Torr vacuum condition.\\n\\nPowder X-ray diffraction (XRD) patterns were recorded by a Bruker D8 diffractometer with Cu K\\u03b1 radiation (\\u03bb = 1.5406 \\u00c5). The surface morphology and elemental compositions were observed by field-emission scanning electron microscopy (FE-SEM; Quanta 250FEG) with energy dispersive X-ray spectroscopy (EDS). X-ray photoelectron spectroscopy (XPS) measurements were carried out on an RBD upgraded PHI-5000C ESCA system (Perkin Elmer) with Mg K\\u03b1 radiation (h\\u03bd = 1486.6 eV). Electrochemical impedance spectroscopy (EIS) was performed under dark condition by using a potentiostat (Solartron 1287) equipped with a frequency response analyzer (Solartron 1255B) with the frequency ranging from 0.05 to 106 Hz. Absorption spectra were measured with a UV-vis-NIR spectrophotometer (UV-3600, Shimadzu). The PL spectra of the films were obtained at room temperature using a steady-state lifetime spectrofluorometer (Varian Cary Eclipse) with an excitation wavelength of 530 nm. The current\\u2013voltage characteristic curves were measured under standard AM 1.5 sunlight (100 mW cm\\u22122, WXS-90L2, Wacom). The effective area of the cell was calculated as 0.09 cm2 using a non-reflective metal mask.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 180,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: 13.02,\\n Stability_PCE_end_of_experiment: 5,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"4-hydroxy phenethylamine hydrochloride (0.5\\u202fg, 2.88\\u202fmmol) and P2O5 (0.82\\u202fg, 5.78\\u202fmmol) was dissolved in H3PO4 (85%, 5\\u202fmL) and the mixture was stirred under 80\\u202f\\u00b0C for 24\\u202fh under Ar atmosphere. The mixture was cooled to room temperature and then dissolved in 25\\u202fmL deionized water. Then excess NaHCO3 was added until the pH\\u202f>\\u202f10. After removal of the solution, the residue was purified by column chromatography (SiO2, CH2Cl2/MeOH\\u202f=\\u202f1/1) to give EAPP (0.42\\u202fg, 68%) as a white solid. 1H NMR (400\\u202fMHz, CD3OD, 298\\u202fK): \\u03b4 7.02 (d, J\\u202f=\\u202f8.4\\u202fHz, 2H), 6.72 (d, J\\u202f=\\u202f8.4\\u202fHz, 2H), 2.81 (t, J\\u202f=\\u202f7.2\\u202fHz, 2H), 2.65 (t, J\\u202f=\\u202f7.2\\u202fHz, 2H). HRMS (ESI) (m/z): [M-Na+]\\u2212 calcd for C8H10NNaPO4, 238.0251; found, 238.0261.\\n\\nThe fluorine-doped tin oxide-coated glasses were sequentially cleaned by ultrasonication in a deionized water bath with Triton X-100 (1:100 by volume) and isopropanol 30\\u202fmin. The substrates were further cleaned by ultraviolet ozone treatment for 15\\u202fmin. A dense compact layer (cl-TiO2, \\u223c80\\u202fnm in thickness) was deposited onto the cleansed FTO by spray pyrolysis at 500\\u202f\\u00b0C. 20\\u202fmM titanium diisopropoxide bis(acetylacetonate) in anhydrous isopropanol was used as the precursor and N2 as carrier gas. After cooling down to room temperature, the substrates were treated in a 0.01\\u202fM aqueous solution of TiCl4 for 40\\u202fmin at 70\\u202f\\u00b0C, rinsed with deionized water and annealed at 500\\u202f\\u00b0C for 20\\u202fmin. A 150\\u2013200\\u202fnm TiO2 (mp-TiO2) films were coated on the cl-TiO2/FTO substrate by spin coating at the speed of 4500\\u202frpm for 20\\u202fs with the ramp-up speed of 2000\\u202frpm/s using a diluted particle paste in ethanol (1:5.5, weight ratio). After drying at 100\\u202f\\u00b0C for 10\\u202fmin, the TiO2 films were gradually sintered to 500\\u202f\\u00b0C for 30\\u202fmin.\\nThe perovskite precursor solution (1.4\\u202fM) were prepared by dissolving CH3NH3I (MAI), PbI2 and 1\\u202fmol% EAPP in dimethyl sulfoxide (DMSO) at 70\\u202f\\u00b0C for 12\\u202fh. The molar ratio of PbI2 and the overall organic ammonium cations was maintained at 1:1. The precursor solution was spin coated onto the mp-TiO2/cl-TiO2/FTO substrate in an N2 flowing glovebox: firstly 1000\\u202frpm for 10\\u202fs with ramp-up speed of 1000\\u202frpm/s, secondly, 6000\\u202frpm for 30\\u202fs with 3000\\u202frpm/s. During the second step, toluene (800\\u202f\\u03bcL) was dropped on the center of the substrate 20\\u202fs prior the end of the procedure. The substrate was immediately annealed on a hotplate at 100\\u202f\\u00b0C for 30\\u202fmin. After cooling down to room temperature for few minutes, a spirofluorene-linked methoxy triphenylamines (Spiro-OMeTAD) solution (60\\u202fmM in chlorobenzene) was spin-coated on top of perovskite layer at 3000\\u202frpm for 30\\u202fs. In addition, 28.8\\u202f\\u03bcL of tertbutylpyridine and 18.5\\u202f\\u03bcL of acetonitrile solution containing 520\\u202fmg/mL Li-bis(trifluoromethaanesulfonyl) imide (Li-TFSI) and 7.9\\u202f\\u03bcL of tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) tris(trifluoromethaanesulfonyl imide) were added into Spiro-OMeTAD solution (60\\u202fmM in chlorobenzene). Finally, 80\\u202fnm of Ag was deposited as counter electrode through thermal evaporation under a base pressure of 4\\u202f\\u00d7\\u202f10\\u22127 torr at a rate of 0.2\\u202f\\u00c5/s for first 10\\u202fnm and 0.6\\u202f\\u00c5/s for second 70\\u202fnm.\\n\\nNuclear magnetic resonance (NMR) characteristics was performed by dissolving the perovskite films in deuterated DMSO with Bruker-AVANCE III HD 500\\u202fMHz. The surface morphology of films was investigated using a high-resolution field emission scanning electron microscope (SEM) (Carl Zeiss Microscopy GmbH Supra 55). X-ray diffraction (XRD) was performed with a Bruker D8 Advance powder diffractometer using Cu K\\u03b1 1/2 source in \\u03b8-\\u03b8 model. The absorption (Abs) spectra of the perovskite films on FTO were measured by UV\\u2013vis spectrophotometer (Agilent cary5000) using an integrating sphere accessory. The in-situ transmittance measurements were carried out every 5 mins (30 mins in total) using double-beam model (22\\u202f\\u00b1\\u202f1\\u202f\\u00b0C, 45\\u202f\\u00b1\\u202f2% RH).\\nThe Current-voltage (J-V) characteristics were examined under AM 1.5\\u202fG solar illumination at 100\\u202fmW/cm2 (1 sun) using a Keithley 2400 source unit. The light intensity was calibrated by means of a KG-5 Si diode with a solar simulator (Enli Tech, Taiwan). The spectral mismatch correction factor is 0.49%. The devices were conducted in reverse scan (1.2\\u202fV to \\u22120.1\\u202fV, step 0.02\\u202fV) or forward scan (-0.1\\u202fV to 1.2\\u202fV, step 0.02\\u202fV), and the delay time was 30\\u202fms. The J-V curves for all devices were measured by masking the active area using a metal mask with an area of 0.04\\u202fcm2. Devices were stored (without encapsulation or light blocking) and tested in the same nitrogen filled glovebox of thermal evaporation, with O2\\u202f<\\u202f3\\u202fppm, H2O\\u202f<\\u202f1\\u202fppm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: EAPP,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 100,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 98,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Cesium lead iodide was prepared by the two-step solution process. Initially, 0.5\\u202fM cesium iodide and 0.5\\u202fmM PEG were well dispersed in the DMF solution. After that 0.5Mof lead iodide was added to this solution. This solution transport into silica crucible and kept in the 350\\u202f\\u00b0C for 30\\u202fmin. Black color cubic nature of the cesium lead iodide was formed. The collected CsPbI3 was kept vacuum desiccator. The same procedure was followed by the preparation of the cesium lead iodide without the PEG.\\nTiO2 paste was spin-coated on the FTO glass plate with 10\\u202f\\u03bcL of the perovskite solutions of PEG stabilized synthesis of the CsPbI3 coated on the 2000\\u202frpm for 40\\u202fs and then annealed in air at 60\\u202f\\u00b0C for 45\\u202fmin. HTM solution containing 0.8\\u202fmol of Spiro-OMeTAD was deposited on the TiO2 paste. After 5\\u202fmin HTM solution was travel to 0.5\\u202fcm2 areas of the photo-anode. FTO/TiO2/PEG-CsPbI3/Spiro-OMeTAD based substrate was heating at 45\\u202f\\u00b0C for 10\\u202fmin under Nitrogen gas atmosphere. 2\\u202fml of the gold chloride trihydrate was coated on the FTO glass plate and then applying the 80\\u202f\\u00b0C of the for15\\u202fmin and thus used as a back electrode. FTO-TiO2/PEG-CsPbI3/Spiro-OMeTAD/Au/FTO was assembled the perovskite device. Similar way to prepare the neat cesium lead iodide based perovskite solar cell device.\\nThe surface morphology of the PEG unstabilized and stabilized CsPbI3 was characterized by HR-SEM and TEM with their SAED pattern. The crystalline structures were examined by X-ray diffraction. The functional group identification was confirmed by FT-IR spectroscopy. Photovoltaic performance of the PSCs was measured using a solar simulator (Model 69907, Oriel) and Keithley source meter under illumination of AM 1.5G light, mask with a window of 0.15\\u202fcm2 was clipped on the TiO2 side to define the active area of the cells.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: PEG,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au | FTO,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Spin-coating | Sandwiching,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 600,\\n Stability_PCE_initial_value: 2.63,\\n Stability_PCE_end_of_experiment: 98,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium diisopropoxide (bis-2,4-pentanedionate) and the SnO2 colloid precursor (tin(IV) oxide, 15% in H2O colloidal dispersion) were purchased from Alfa Aesar. [6,6]-phenyl-C61-butyric acid methyl eater (PCBM) and C60-SAM were purchased from Lumtec, Taiwan. Formamidinium iodide (FAI), methylammonium bromine (MABr), and lead bromine (PbBr2) were purchased from Lumtec, Taiwan. Lead iodide (PbI2) was obtained from Alfa Aesar. Spiro-OMeTAD was purchased from Shenzhen Feiming Science and Technology Co., Ltd. All of the solvents were obtained from Aladdin, Alfa Aesar or Sigma-Aldrich.\\n\\nFTO glass was etched by a femtosecond laser device (Co-developed with the support of Wuhan Hongtuo co. LTD, SN: HT-TCR-1030-001), and then ultrasonic cleaning by detergent solution, pure water and ethyl alcohol for 20 min, respectively. The transmittance of glass/FTO substrates in the region is almost 85%. The titanium diisopropoxide (bis-2,4-pentanedionate) was diluted into 1/10 using isopropanol by volume before used. For compact TiO2 blocking layer, the diluted titanium diisopropoxide (bis-2,4-pentanedionate) was pyrolysis on the FTO glass (cleaned by UV-ozone for 15 min) at 450 \\u00b0C by spraying and then cooling to room temperature. The thickness of the TiO2 film is approximately 20 nm. For TiO2/C60 and TiO2/PCBM stacking layers, a 25 \\u03bcL C60 (5 mg C60 dissolved in 1 mL chlorobenzene) or PCBM (5 mg PCBM dissolved in 1 mL chlorobenzene) solution was spin coated on the compact TiO2 substrate. For a thickness of 18 nm SnO2 nanoparticles blocking film, the nanoparticles solution which was diluted to 37.5 mg/mL and then spin coated on the FTO glass at 3000 rpm for 30 s followed by annealing at 150 \\u2103 for 30 min. As for the stacked n-layer film, the TiO2 layer was prepared by the above method, and then coated SnO2 layer. The perovskite layer was deposited by spun a FA0.85MA0.15Pb(I0.85Br0.15)3 precursor solution (1.4 M) at 6000 rpm for 30 s with an accelerated speed of 1000 rpm, which was composed of 0.85 PbI2 and 0.15 PbBr2, and 1.3 M organic cation which are composed of 0.85 FAI and 0.15 MABr in a mixed solvent of DMF and DMSO with a volume ratio of 4:1. When the perovskite solution was spin-coated at the last fifth seconds, 90 \\u03bcL of Ethyl acetate (EA) was dropped on the spinning substrate. To form a smooth and no pinhole precursor film, EA was required to drop slowly so that allow sufficient extraction of extra DMSO through the perovskite film. The films were then post-annealed at 120 \\u00b0C for 50 min immediately, and after cooling down to room temperature, the HTL layer was spun on the mixed perovskite films at 3000 rpm for 30 s using an ethyl acetate (EA) solution which prepared by dissolving 41.6 mg Spiro-OMeTAD into 1 mL EA and doped by a molar ratio of 3.3 4-tert-butylpyridine, 0.3 Li-TFSI, and 0.03 FK209. Finally, 80 nm Au contact was evaporated as the back electrode to form the whole devices.\\n\\nThe photocurrent density-voltage curves of the perovskite solar cells were measured using a solar simulator (Oriel 94023 A, 300 W) and a Keithley 2400 source meter. The intensity (100 mW/cm2) was checked with a standard Si solar cell (Oriel, VLSI standards, Newport). All the devices were tested in ambient air under AM 1.5G sun light (100 mW/cm2) using a metal mask of 0.16 cm2 with a scan rate of 10 mV/s and a metal mask of 10 cm2 (5 \\u00d7 5 cm2 module) with a scan rate of 50 mV/s. The steady-state PCE was measured by setting the bias voltage to the VMPP (the VMPP at maximum power point was determined from the J-V curve) and tracing the current density. EQE measurements were performed using an internal establishment system with monochromatic light and white bias light (~0.1 Sun). The photodiode used for the calibration of EQE measurements has been calibrated by Newport.\\nThe surface morphologies and microstructures of the prepared TiO2, SnO2, stacked n-layer, perovskite film and cross-sectional structure of the whole perovskite solar cells were tested using a field-emission scanning electron microscopy (FESEM, Zeiss Ultra Plus). The surface morphology of perovskite films and different ETL films were tested by atomic force microscope (AFM, SPM9700, Shimadzu, Japan). X-ray diffraction patterns (\\u03b8\\u22122\\u03b8 scans) of SnO2 nanoparticles and different ETL processed perovskite film were taken on an X-ray diffractometer (XRD, D8 Advance). The SnO2 nanoparticles treated by different temperature were tested by a fourier transform infrared spectroscopy (FTIR, Nicolet 6700, USA). The different ETL processed perovskite film were also tested by UV\\u2013vis (lambda 750S, PerkinElmer). The EIS were carried out by a EC-lab (SP300). The steady-state PL and time-resolved PL decay spectrum was measured by fluorescence spectrometer (FLS 980), with a 507 nm laser (EPL-510, Edinburgh Instruments Ltd). UV stability tests by a 365 nm UV generator with power around 172 mW/cm2. Stability of the solar cells were tested using a commercial environmental chamber (Atlas SC3 600 MHG).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 50,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 2160,\\n Stability_PCE_initial_value: 17.46,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium tetrachloride, Lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) and 4-tert-butylpyridine (tBP) were purchased from Sigma-Aldrich. Lead iodide (PbI2, 99.99%), Silver iodide (AgI, 99.99%) and chlorobenzene were obtained from Alfa Aesar Ltd. Spiro-OMeTAD was purchased from 1-Material Ltd. The precursor solution was prepared by dissolving MAI:PbI2 (1.2\\u202fmol: 1.2\\u202fmol) in 1\\u202fmL coalescing solvents of dimethyl sulfoxide (DMSO) and 1,4-butyrolactone (GBL) (3:7, v/v) to make MAPbI3 solution. Spiro-OMeTAD precursor was obtained by dissolving in chlorobenzene, which Li-TFSI and tBP were added into about 2\\u202fh later. Then AgI, which was dissolved in Dipropyl sulfide, was added to Spiro-OMeTAD solutions for doping.\\n\\nAs a substrate, fluorine-doped tin oxide (FTO) coated glass (\\u223c15\\u202f\\u03a9/sq) was sequentially cleaned in neutral detergent, acetone, and ethanol in ultrasonic cleaning machines for 15\\u202fmin. After UV ozone treatment for 20\\u202fmin, the substrate was covered with a compact 100\\u202fnm TiO2 layer by using titanium tetrachloride (TiCl4) and water as the precursors of solution deposition at 70\\u202f\\u00b0C for 1\\u202fh. And then, the perovskite solution was added onto the TiO2 layer by a consecutive two-step spin-coating process at 2000 and 4000\\u202frpm for 20 and 40\\u202fs, respectively, where a chlorobenzene drop-casting was carried out as an anti-solvent 40\\u202fs later. Afterwards, the film was annealed at 100\\u202f\\u00b0C for 10\\u202fmin in nitrogen glove box. The Ag+-doped or undoped Spiro-OMeTAD solutions were then spin-coated onto the perovskite layer at 5000\\u202frpm for 40\\u202fs. After air-oxidation for 15\\u202fh, the device was finally added with electrodes for MoO3 (8\\u202fnm) and Ag (100\\u202fnm) by vacuum-evaporating at a rate of 0.2 and 3\\u202f\\u00c5\\u202fs\\u22121, respectively. The active area of each device was 9\\u202fmm2 defined through a shadow mask.\\n\\nCurrent density-voltage characteristics of perovskite solar cells under 1 sun illumination were performed using a programmable Keithley 2400 source meter under AM 1.5G solar irradiation at 100\\u202fmW/cm2 with constant and low scan speed of 0.1\\u202fmV/S (Newport, Class AAA solar simulator, 94023A-U). The optical microscopy images (OM, Leica DM4 M) were achieved to display surface morphology. Also, atomic force microscopy images were obtained using a Veeco Multimode V instrument to evaluate the surface morphology of films in tapping mode. XRD patterns of the perovskite films were performed by PANalytical 80 equipment (Empyrean, Cu Ka radiation). The absorption spectra of perovskite films were obtained by a UV\\u2013vis spectrophotometer (PerkinElmer Lambda 750). The stability of the devices was evaluated after exposure to ambient air without any wrap (12% for Humidity and 20\\u202f\\u00b0C for temperature). The consistency of each test condition is ensured in the test process.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 20.0; 20.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 120,\\n Stability_PCE_initial_value: 17,\\n Stability_PCE_end_of_experiment: 75,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The molecule IDIC was synthesized by one-step simple Knoevenagel condensation, according to our previously published procedure. Unless stated otherwise, all reagents were obtained commercially and were used without further purification. PbI2 (99.999%), N,N-dimethylformamide (99.99%), isopropanol (99.99%) and chlorobenzene (99.9%) were purchased from Sigma-Aldrich. Aminomethane (CP) and ethanol (AC) were purchased from Beijing Chemical Works. Hydrogen iodide (57%) was purchased from Alfa Aesar. Spiro-OMeTAD was purchased from Luminescence Technology Corp.\\n\\nPSCs were fabricated with a structure of ITO/ETL/CH3NH3PbI3(Cl)/spiro-OMeTAD/Au. The indium tin oxide (ITO) glass was pre-cleaned in an ultrasonic bath of detergent water, ultrapure water, acetone and isopropanol successively. For reference devices based on TiO2, a TiO2 nanoparticle suspension in ethanol (5.3 mg mL\\u22121) with an appropriate amount of titanium diisopropoxide bis(acetylacetonate) was spin coated onto an ITO glass substrate and annealed at 150 \\u00b0C for 30 min in air to form an ETL (40 nm thick). Next, the substrates were transferred into a nitrogen-filled glovebox. For the IDIC-based devices, the ITO glass was treated with ultraviolet ozone for 20 min and transferred into a nitrogen-filled glovebox. The IDIC solution (4 mg mL\\u22121 in chloroform) was subsequently spin-coated onto the ITO substrates at 4000 rpm for 60 s and annealed at 70 \\u00b0C for 10 min. Then a solution of PbI2 (dissolved in DMF, 450 mg mL\\u22121) was spin-coated on TiO2 and IDIC substrates at 3000 rpm for 30 s and annealed at 70 \\u00b0C for 20 min. A mixture of CH3NH3I (50 mg mL\\u22121) and CH3NH3Cl (5 mg mL\\u22121) dissolved in isopropanol was spin-coated onto the dried PbI2 layer at 3000 rpm for 30 s. The obtained films were annealed at 150 \\u00b0C for 15 min in air. The doped spiro-OMeTAD was spin-coated at 3000 rpm for 30 s at a concentration of 80 mg mL\\u22121 with the addition of 35 \\u03bcL of Li-TFSI/acetonitrile (260 mg mL\\u22121) and 28 \\u03bcL of 4-tert-butylpyridine. Finally, an 80 nm gold layer was deposited on the top of spiro-OMeTAD through shadow masks via thermal evaporation under high vacuum (\\u223c2 \\u00d7 10\\u22126 Torr).\\n\\nThe current density\\u2013voltage (J\\u2013V) characteristics of photovoltaic devices were obtained using a Keithley 2400 source-measure unit under simulated sunlight from an Oriel 300 solar simulator, and the light intensity was calibrated using a KG-5 Si diode. The effective area of each cell was 0.102 cm2 defined by masks for all the photovoltaic devices discussed in this work. The EQE spectrum was measured using a Solar Cell Spectral Response Measurement System QE-R3011 (Enlitech Co., Ltd). The light intensity at each wavelength was calibrated using a standard single crystal Si photovoltaic cell. The UV-visible absorption spectra were measured using a UV-visible spectrophotometer (Agilent 8453). AFM images were obtained by using a Multimode 8 scanning probe microscope (Bruker). The top-view and cross-sectional SEM images were obtained using a scanning electron microscope (Hitachi S4800). The XRD spectra were obtained using a D/MAX 2400 diffractometer with Cu K\\u03b1 radiation (Rigaku). Steady-state PL and time-resolved transient-state PL were measured by using an FLS980 (Edinburgh Instruments Ltd) with an excitation at 470 nm. Transient photovoltage (TPV) and photocurrent (TPC) measurements were performed with a self-designed system excited with a 532 nm (Brio, 20 Hz, 4 ns) pulsed laser. A digital oscilloscope (Tektronix, DPO 7104) was used to record the photocurrent or photovoltage decay process with a sampling resistor of 50 \\u03a9 or 1 M\\u03a9, respectively. Static contact angles were measured on a Dataphysics OCA25 contact-angle system at ambient temperature (the test liquid is water). The thickness of the IDIC layer was measured using a Bruker Dektak-XT. All the measurements of the solar cells were performed under an ambient atmosphere at room temperature without encapsulation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 150,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 15.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 168,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 30,\\n Cell_area_measured: 0.102,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were purchased from commercial suppliers as mentioned and used as received unless otherwise specified. Caesium iodide (CsI, 99% purity) and bismuth iodide (BiI3, 99% purity) were purchased from Sigma Aldrich. We prepared 0.5 M precursor solutions (CsBi3I10 (CBI-1) and Cs3Bi2I9 (CBI-2)) by dissolving the CsI and BiI3 powder at the molar ratios of 1:3 and 3:2 in DMF and DMSO (7:3 (v:v)) at 70 \\u00b0C for 12 hours, respectively. The BiI3 precursor solution was prepared by dissolving 50\\u2013150 mg mL\\u22121 in DMF at 70 \\u00b0C for 12 hours in a N2-filled glove box. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) (Clevios, Al4083) was diluted by mixing with methanol at the ratio 3:7. The poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA) (0.5 wt%) and [6,6]-phenyl C61 butyric acid methyl ester (PC61BM) [Sigma Aldrich, 99% purity] solutions (2 wt%) were dissolved in anhydrous chlorobenzene (CB) at 50 \\u00b0C for 7 hours. Aluminium-doped zinc oxide (AZO) nanoparticle ink (Avantama, N-21X) was used. All solutions were filtered using 0.45 \\u03bcm syringe filters to avoid unwanted particles in the precursor solutions.\\n\\nSolar cell devices were fabricated on pre-cleaned patterned indium tin oxide (ITO)-coated glass substrates (15 \\u03a9 square\\u22121). The ITO substrates were pre-cleaned in an ultrasonic bath with detergent, pure water, and 2-propanol, followed by an ultraviolet-ozone treatment for 5 min to remove organic residuals. A thin PTAA HTM layer (\\u223c20 nm) was deposited onto the ITO substrate by spin coating at 4000 rpm (2000 rpm s\\u22121 speed) for 30 seconds and subsequently dried at 100 \\u00b0C for 10 min on a hot plate in ambient nitrogen. Similarly, another thin HTM layer (\\u223c30 nm) (PEDOT:PSS) was deposited onto the ITO substrate by spin coating at 3000 rpm for 30 seconds and subsequently dried at 130 \\u00b0C for 30 min on a hot plate in ambient air. The NiOx (\\u223c30 nm) film was deposited by sputtering as mentioned in our earlier report. For the fabrication of the Bi-based based thin film, the precursor solution (CsBI-1 or CsBI-2 or BiI3) was spin coated at 1500 rpm for 20 s (ramping rate 500 rpm s\\u22121) and 3000 rpm for 30 s. After spin coating, the films were crystallized by conventional annealing (CA) at various temperatures (90, 120, 150, 180, and 200 \\u00b0C) for 60 minutes. For antisolvent (AS)-treated samples, 150 \\u03bcL chlorobenzene was dripped 20 s after starting spin coating and annealed at 120 \\u00b0C for 60 minutes. The solvent annealing of post antisolvent (AS)-dripped samples was carried out by putting about 5 \\u03bcL of DMF at the edge of a cover glass at 120 \\u00b0C for 60 minutes. For ETL, PC61BM was spin-coated on top of the Bi-HaP films at 800 rpm for 30 s, then at 4000 rpm for 10 s, and annealed at 100 \\u00b0C for 10 min. Then, a thin electron selective layer (ESL) of AZO was deposited by spinning at 2000 rpm for 20 s and dried by annealing at 100 \\u00b0C for 10 min. The device structure was completed by depositing 100 nm thermally evaporated Ag at <10\\u22124 Pa. We sealed our devices of area \\u223c0.26 cm2 using UV-curable resins.\\n\\nThe X-ray diffraction (XRD) patterns of the fabricated films were obtained using the Bruker D8 advance x-ray diffractometer (CuK\\u03b1 radiation, \\u03bb = 1.54050 A). The morphologies of the films and cross-sectional images were obtained by a high-resolution scanning electron microscope (SEM) at 5 kV accelerating voltage (Hitachi, S-4800). The absorption spectra and photoluminescence (PL) spectra of various films were measured using a UV-Vis-NIR spectrometer (7200, V-Jasco) and spectrofluorometer (FP8500, Jasco), respectively. Raman spectra were obtained using a micro Raman spectrometer (Horiba, green laser 532 nm). The HOMO levels of transport layers were measured using a photoelectron spectrometer (Riken Keiki, AC-3). XPS spectra were obtained using a VersaProbe II (ULVAC-PHI, Japan). The current density\\u2013voltage (J\\u2013V) curves were measured at the scan rate of 0.05 V s\\u22121 under 1 sun with an AM 1.5G spectral filter (100 mW cm\\u22122) coupled with an MPPT system (Systemhouse Sunrise Corp.). The external quantum efficiency (EQE) spectra were obtained using a spectrometer (SM-250IQE, Bunkokeiki, Japan). Capacitance\\u2013frequency response (C\\u2013f) was obtained using an LCR meter (E4980A, Agilent), which probes from 20 Hz to 2 MHz at the AC voltage amplitude of 30 mV under dark conditions. After confirming the geometric capacitance regime in C\\u2013f spectra, capacitance\\u2013voltage (C\\u2013V) measurements were carried out at 10 kHz (the geometric capacitance regime in C\\u2013f spectra).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | AZO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs3Bi2I9,\\n Perovskite_composition_short_form: CsBiI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Sputtering,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Ambient,\\n Stability_time_total_exposure: 720,\\n Stability_PCE_initial_value: 1.3,\\n Stability_PCE_end_of_experiment: 100,\\n Cell_area_measured: 0.26,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, P VP AI4083) was purchased from Heraeus Clevios. Nickel phthalocyanine-3,4\\u2032,4\\u2032\\u2032,4\\u2032\\u2032\\u2032-tetrasulfonated tetrasodium (NiPcS4) was synthesized following the procedure in literature, and was characterized by HRMS and UV-vis absorption spectrum (ESI\\u2020). Lead acetate trihydrate (PbAc2\\u00b73H2O) was purchased from Aladdin Industrial Corporation. Methylamine iodide (MAI) was purchased from Xi'an Polymer Light Technology Corporation. 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) was purchased from SunaTech Inc. PC61BM was purchased from Nano-C Tech. DMF, isopropyl alcohol (IPA), and chlorobenzene (CB) were purchased from Sigma-Aldrich. ITO was purchased from Wu Han Jinge Solar Energy Technology Co. Ltd. China.\\n\\nVarious weight ratios of NiPcS4 (5, 10, 20, and 30 wt%) were added to the aqueous PEDOT:PSS solutions. Following this, the resulting solutions were magnetically stirred for more than three hours at room temperature, and then filtered by polytetrafluoroethylene (PTFE) filters (0.45 \\u03bcm) and subsequently utilized for thin films' fabrication. The NiPcS4-treated PEDOT:PSS thin films were prepared through spin-coating the above blended solutions, followed by thermal annealing at 140 \\u00b0C for about twenty minutes in air. The thicknesses of NiPcS4-treated PEDOT:PSS thin films was regulated by varying the spin-rate from 2000 to 5000 rpm.\\n\\n3MAI:PbAc2\\u00b7xH2O precursor solutions were prepared according to our previously reported method. To generate the 3MAI:PbAc2\\u00b7xH2O precursor solution with x equal to 0, PbAc2\\u00b73H2O was first heated to 110 \\u00b0C for 12 h in a glove box to obtain anhydrous PbAc2. PbAc2\\u00b7xH2O was then obtained by mixing PbAc2 with PbAc2\\u00b73H2O at a molar ratio of (3 \\u2212 x):x. Finally, MAI and PbAc2\\u00b7xH2O were dissolved in anhydrous N,N-dimethylformamide at a 3:1 molar ratio with the concentration of 45 wt% (optimal x = 2.8).\\n\\nThe device structure is ITO/HTL/perovskite CH3NH3PbI3/PC61BM/BCP/Ag, in which HTL is one of NiPcS4, PEDOT:PSS, or mixed NiPcS4\\u2013PEDOT:PSS. Patterned ITO coated glass substrates were sequentially cleaned in detergent, deionized water, acetone, and isopropanol. The substrate was then desiccated in an oven, before treating in an ultraviolet-ozone chamber for about twenty minutes. Pristine PEDOT:PSS, NiPcS4, or mixed PEDOT:PSS\\u2013NiPcS4 aqueous solutions filtered by a 0.45 \\u03bcm filter tip were spin-coated at around 4000 rpm for approximately 50 seconds on ITO electrodes, before baking at 140 \\u00b0C for about 20 minutes in the ambient atmosphere. Subsequently, the substrates were shifted to a nitrogen-filled glove-box, where a \\u2248400 nm-thick CH3NH3PbI3 perovskite layer was deposited on the surface of either the pristine PEDOT:PSS layer, NiPcS4 layer or mixed NiPcS4\\u2013PEDOT:PSS layer through a one-step solution casting approach. Detailed procedures were according to our previously reported method: perovskite films were spin-coated from set 80 \\u00b0C precursor solutions at a speed of around 4000 rpm for about 50 seconds, in which the substrate temperature was maintained at 90 \\u00b0C; then, they were annealed on a hotplate at 90 \\u00b0C for another 10 minutes. After cooling to room temperature, PC61BM (dissolved in CB, 20 mg mL\\u22121) was spin-coated over the perovskite layer at 1000 rpm for another 30 seconds, and finally annealed at 80 \\u00b0C for 30 min. After cooling to room temperature, C60 (20 nm), BCP (8 nm) and the metal silver (100 nm) electrode were thermally evaporated in a vacuum chamber at pressure set at <4 \\u00d7 10\\u22124 Pa through a shadow mask. Photoactive regions of the devices were 0.08 cm2.\\n\\nThe J\\u2013V measurements of the devices under AM1.5 G solar 100 mW cm\\u22122 simulator illumination (Enlitech Solar Simulator SS-F5-3A) was performed on a computer-controlled Keithley 2400 Source Measure Unit in air (60% humidity) at room temperature without encapsulation. The external quantum efficiency (EQE) was measured under ambient atmosphere at room temperature using a DSR100UV-B spectrometer with a SR830 lock-in amplifier. The steady-state PCE was measured by monitoring current with the largest power output bias voltage and recording the value of the photocurrent. A xenon lamp was used as the light source.\\n\\nThe AFM images were obtained by the Bruker Dimension Icon in the ScanAsyst mode. Scanning electron microscopy (SEM) images were obtained by the field-emission SEM (FEI Nova_Nano SEM 430). The X-ray diffraction patterns were obtained by a Bruker ECO D8 (Bruker, Germany). The ultraviolet-visible (UV-vis) absorption spectra of the perovskite films were obtained by the spectrophotometer (Perkin Elmer Lambda 750). UPS analysis was conducted to measure the energy level of HTLs with an unfiltered He I (21.22 eV) gas discharge lamp and a hemispherical analyzer.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: NiPcS4,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 480,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 40,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Formamidinium iodide (FAI) and lead iodide (PbI2) were purchased from Dyesol and Acros, respectively. Cesium iodide (CsI), anhydrous N,N-dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), chlorobenzene (CB), toluene and isopropanol (IPA) were obtained from Sigma-Aldrich. Poly-(4-butylphenyl diphenylamine) (poly-TPD) was bought from Xi'an Polymer Light Technol. Corp. All chemicals were directly used as received.\\n\\nIn our proposed method (denoted as the coupled method), the PbI2\\u2013(CsI)0.15\\u2013(FAI) intermediate complex films were first deposited on preheated poly-TPD/ITO substrates (80 \\u00b0C) by spin-coating a hot precursor solution (80 \\u00b0C) at 3000 rpm for 40 s, during which 200 \\u03bcl toluene was poured onto the substrate. The precursor solution consists of 461 mg PbI2, 39 mg CsI, 79 \\u03bcl DMSO, 1 ml DMF and different amounts of FAI. The amount of CsI is set constant, corresponding to an atomic ratio of 15%, whereas the atomic ratio of FAI ranges from 0 to 85% (corresponding to PbI2). The intermediate complex films, except for the case of PbI2\\u2013(CsI)0.15\\u2013(FAI)0.85, were then annealed at 80 \\u00b0C for 5 min, followed by the spin-coating of FAI (30 mg ml\\u22121 in IPA) at 3000 rpm for 40 s. The resulting perovskite precursor films were finally annealed at 140 \\u00b0C for 1 h and washed by spin-coating with 100 \\u03bcl IPA. All the above processes were carried out in ambient air with a RH of 70 \\u00b1 10%.\\nFor comparison, devices were also fabricated by premixing-only, preheating-only and non-intermediate methods. In the case of the premixing-only method, the amount of FAI premixed into the precursor solution in the first step corresponded to an atomic ratio of 30% (relative to PbI2), and all the precursor solutions and substrates were at room temperature without any preheating. All other procedures were the same as the coupled method. In the cases of the latter two, as compared to the coupled method, the only difference lied in the precursor solutions. Specifically, for the non-intermediate method, the precursor in the first step was changed to a hot PbI2 solution (461 mg PbI2 in 1 ml DMF and 79 \\u03bcl DMSO, 80 \\u00b0C), and the precursor solution in the second step was changed to a hot CsI/FAI IPA solution (12 mg CsI and 45 mg FAI in 1 ml IPA, 80 \\u00b0C). As for the preheating-only method, the precursor solution in the first step consisted of 461 mg PbI2, 39 mg CsI, 79 \\u03bcl DMSO and 1 ml DMF, while the precursor solution in the second step was a hot FAI solution (45 mg ml\\u22121 in IPA).\\n\\nIndium tin oxide (ITO) glass substrates were successively washed with decon 90, deionized water and isopropanol and dried in an oven. Prior to device fabrication, the ITO glass substrates were subjected to an ultraviolet-ozone (UVO) treatment for 20 min. After that, a poly-TPD in CB solution, with a concentration of 4 mg ml\\u22121, was spin-coated on the ITO at 6000 rpm for 40 s and annealed at 120 \\u00b0C for 10 min. To tune its surface hydrophilicity, the poly-TPD layer was subjected to a UVO exposure for 20 s. Afterwards, the perovskite layer was deposited onto the modified poly-TPD according to the methods described above. Subsequently, a 20 nm-thick fullerene layer (C60), 8 nm-thick 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline layer (BCP) and Ag electrode (70 nm) were successively deposited atop by thermal evaporation. The active area of the device was 0.1 cm2.\\n\\nThe morphology of the samples was monitored by scanning electron microscopy (Philips XL30 FEG). UV-vis absorption spectra were recorded on a UV-vis spectrometer (PerkinElmer model Lambda 2S). As the substrate has a huge impact on the quality of the perovskite film atop, the samples used for UV-vis measurement have the configuration of perovskite/poly-TPD/ITO. Prior to the measurement, two identical poly-TPD/ITO substrates were used for calibration, one of which was then replaced by the samples, and the other was used as the reference. The detector automatically recorded the intensity of the incident light passing through the sample and reference, which were termed as I and Io, respectively, thus acquiring the absorption spectra. The thickness of the perovskite films was determined by using a surface profilometer (Veeco Dektak 150). X-ray diffraction characterization was carried out on a D2 Phaser instrument with Cu K\\u03b1 (\\u03bb = 0.154 nm) radiation. Steady-state and time-resolved photoluminescence spectra were acquired on a time correlated single photon counting spectrometer from Edinburgh Instruments (LifeSpec II), and the samples were excited with a 485 nm laser. The current\\u2013voltage characteristics of the devices were obtained on a Keithley 2400 source meter under one sun illumination (AM 1.5G, 100 mW cm\\u22122), and the scan rate was 10 mV s\\u22121. The external quantum efficiency and device reflectance measurements were conducted on a home-built set-up. The photo-durability was tested by tracking the current density of a continuously working device (unencapsulated) exposed to one sun illumination in ambient air (RH: 70 \\u00b1 10%), and the device was subjected to a voltage bias of 0.76 V, corresponding to its maximum power point. The thermal stability was evaluated by measuring the J\\u2013V characteristics of the devices (85 \\u00b0C, unencapsulated) every few hours in ambient air (RH: 70 \\u00b1 10%).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: Cs0.15FA0.85PbI3,\\n Perovskite_composition_short_form: CsFAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80.0 >> 140.0,\\n Perovskite_deposition_thermal_annealing_time: 5.0 >> 60.0,\\n HTL_stack_sequence: Poly-TBD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 85.0; 85.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 24,\\n Stability_PCE_initial_value: 15.56,\\n Stability_PCE_end_of_experiment: 95,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped tin oxide conducting glass (FTO) was obtained from Pilkington (14 \\u03a9 sq\\u22121). Methylammonium iodide (CH3NH3I), PbBr2, CsI and PbI2 were obtained from TCI. Titanium diisopropoxide dis(acetylacetonate), dimethyl sulfoxide (DMSO) and N,N-dimethylformide (DMF) were purchased from Sigma-Aldrich. Spiro-OMeTAD was purchased from Lumtec Co., Taiwan. Y(NO3)3, hexadecyl trimethyl ammonium bromide (CTAB), NaF and Eu(NO3)3 were purchased from Alfa-Aesar. All chemicals were used as received.\\n\\nNaYF4 and NaYF4:Eu3+ were synthesized by the solvothermal method. In a typical synthesis, 3.0 g of CTAB, 20 mL of methanol and 10 mL of water were mixed together. Then, 1 mL of a Y(NO3)3 aqueous solution (0.5 M) and 3 mL of a NaF aqueous solution (1 M) were added. Finally, the mixture was transferred to a 40 mL autoclave that was sealed and heated at 150 \\u00b0C for about 24 h. The white precipitate was collected by centrifugation. To obtain the NaYF4 colloid, the white product was redispersed in 10 mL of ethylene glycol monomethylether. The NaYF4:Eu3+ colloid was prepared using the same method. The Y(NO3)3 aqueous solution was replaced with the mixture of Y(NO3)3 and Eu(NO3)3. The molarity of the Eu3+ doped in each solution was 2%, 4%, 6%, 8% and the corresponding product was marked as NaYF4:Eu3+-2%, NaYF4:Eu3+-4%, NaYF4:Eu3+-6%, NaYF4:Eu3+-8%, respectively.\\n\\nFTO substrates were ultrasonic cleaned sequentially with detergent, acetone, isopropanol and ethanol. The substrates were then subjected to a plasma treatment for 5 min. The NaYF4:Eu3+ layer was formed by spin-coating the NaYF4:Eu3+ colloid on the back of the FTO. The layer was then annealed under an ambient atmosphere for 30 min at 180 \\u00b0C. To prepare the TiO2 ETL, a 0.15 M titanium diisopropoxide dis(acetylacetonate) solution of 1-butanol was spin-coated on the FTO at 700 rpm for 8 s, 1000 rpm for 10 s and 2000 rpm for 40 s, followed by annealing at 550 \\u00b0C for 30 min. The precursor solution of the Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3 light-absorption layer was prepared by dissolving 163.4 mg FAI, 481.7 mg PbI2, 21.3 mg MABr, 76.7 mg PbBr2 and 50 \\u03bcL CsI (1.5 M in DMSO) in a 950 \\u03bcL anhydrous DMF:DMSO mixture with a 4:1 volume ratio. The precursor solution was stirred at room temperature for 3 h, and then spin-coated on the TiO2 layer by a consecutive two-step process of 1000 rpm and 6000 rpm for 4 s and 20 s, respectively. During the high-speed step, 140 \\u03bcL of chlorobenzene was added dropwise at 15 s. The substrates were then annealed at 100 \\u00b0C for 40 min. A spiro-OMeTAD solution was prepared by dissolving 72.3 mg spiro-OMeTAD in 1 mL of chlorobenzene with additives of 17.5 \\u03bcL Li-TFSI solution (520 mg in 1 mL acetonitrile) and 28.8 \\u03bcL t-BP. The spiro-OMeTAD solution was spin-coated on the perovskite layer at 4000 rpm for 20 s. Subsequently, they were stored in a desiccator for 12 h. Au electrodes (90 nm) were deposited with thermal evaporation deposition. The PSC device with the NaYF4:Eu3+ layer was labeled as PSC-2% (NaYF4:Eu3+-2%), PSC-4% (NaYF4:Eu3+-4%), PSC-6% (NaYF4:Eu3+-6%) and PSC-8% (NaYF4:Eu3+-8%), respectively. The PSC device without the NaYF4:Eu3+ layer was denoted as PSC-blank.\\n\\nThe crystal structure was analyzed with X-ray diffraction (XRD, Cu K\\u03b1 radiation, SmartLab 3 kW, Rigaku, Japan). The morphology was observed using a transmission electron microscope (TEM, Tecnai G2 F20). The thickness was tested using a field emission scanning electron microscope (FESEM, SU8010, HITACHI). The optical transmittance of the NaYF4:Eu3+ film on the FTO substrate was determined with a UV/VIS/NIR spectrophotometer (Lambda950, PE). The current\\u2013voltage (J\\u2013V) characteristic curves were recorded using a Keithley 2400 source meter with simulated solar light coming from an AAA solar simulator (Newport-94043A). The IPCE spectrum was measured with an IPCE measurement system (Newport, USA). The stabilized current density was tested with a electrochemical workstation (CHI 660E). The photoluminescence emission spectra were measured with a Thermo Scientific lumina fluorescence spectrometer. Electrochemical impedance spectra (EIS) were generated with a Zennium electrochemical workstation (IM6) by applying an AC voltage of 10 mV amplitude at 0 V bias. The frequency ranged between 100 mHz and 100 kHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 10,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"MIL-125(Ti) was synthesized by modifying the procedure reported elsewhere . Typically, a mixture of 3.0 g terephthalic acid, 6 ml anhydrous methanol, 1.56 ml Ti(OC4H9)4 and 54 ml dimethylformamide (DMF) were loaded into a 100 ml autoclave with a Teflon cup and heated at 120 \\u00b0C for 20 h. Upon cooling down, the white suspension of MIL-125(Ti) was centrifuged at 4000 rpm for 10 min and washed with anhydrous methanol for several times. The synthesized MIL-125(Ti) were sintered at 380 \\u00b0C for 5 h and 500 \\u00b0C for 30 min to produce porous hier-TiO2 nanostructures.\\nThe 0.1 g porous hier-TiO2 was dispersed in 1 ml ethanol, then added 0.5 ml \\u03b1-terpinol and 0.05 g ethyl cellulose into solution to increase the viscosity, and continuously stirred overnight to form the hier-TiO2 slurry.\\n\\nThe patterned FTO substrates were ultrasonically cleaned using deionized water, acetone and isopropanol, then treated under UV-ozone for 15 min. A compact TiO2 layer with 40 nm thickness was spin-coated on FTO substrate and sintered at 500 \\u00b0C for 30 min. The hier-TiO2 slurry was spin-coated onto compact TiO2 layer and then heated at 500 \\u00b0C for 30 min. Finally, the samples were immersed in 40 mM TiCl4 aqueous solutions for 30 min at 70 \\u00b0C and washed with deionized water and ethanol, followed by annealing at 500 \\u00b0C for 30 min in air. The hier-TiO2 scaffold was scattered on the compacted TiO2 layer. For reference of TiO2 nanoparticles (npt-TiO2) scaffold, the TiO2 nanoparticles (18-NRT) were diluted with ethanol at 1:3.5 mass ratio, and its corresponding fabrication procedure is similar to that of hier-TiO2 scaffold.\\n\\nThe MAPbI3 layer was prepared using a typical two-step spin-coating procedure. 20 \\u03bcl PbI2 solution (1 M, PbI2 in a mixture of DMF/DMSO = 7:3, vol:vol) was spin-coated on hier-TiO2 scaffold layer and dried at 40 \\u00b0C for 3 min. 200 \\u03bcl CH3NH3I (MAI) solution in 2-propanol (8 mg ml\\u22121) was dropped on the PbI2-coated substrate to stay for 2 min, then spun at 4000 rpm for 30 s and heated at 100 \\u00b0C for 30 min to form MAPbI3 layer. Subsequently, 72.3 mg Spiro-OMeTAD (\\u226599.5%, Polymer Light Technology Corp., Xi\\u2019an, China.), 28.8 \\u03bcl TBP and 17.5 \\u03bcl Li-TFSI acetonitrile mixture solution (520 mg ml\\u22121) were dissolved in 1 ml chlorobenzene and then spin-coated onto the perovskite layer to form a 60 nm thickness hole transport layer. Finally, a 80 nm thick AgAl alloy electrode was thermally evaporated onto hole transport layer and the active area of device is 0.10 cm2.\\n\\nThe morphology, structure and composition of the samples were respectively investigated by scanning electron microscopy (SEM, Hitachi S-4800), transmission electron microscopy (TEM, JEM-2100), X-ray diffraction (XRD, Holland Panalytical PRO PW3040/60) with Cu K\\u03b1 radiation (V = 30 kV, I = 25 mA). The light absorption and scattering spectra were measured using a UV\\u2013vis spectrophotometer (Hitachi U-3900). The N2 adsoprtion-desorption isotherms were recorded at 77 K with a Micromeritcs Tristar 3000 analyzer (Tristar, USA). The TiO2 samples were degassed in vacuum at 200 \\u00b0C for 8 h prior to measurement. The Brunauer-Emmett-Teller (BET) method was adopted to calculate the surface area and the Barrett-Joyner-Halenda (BJH) method was used to determine the average pore size. The photocurrent density-voltage (J-V) curves were measured using a Keithley model 2440 Source Meter under the illumination of AM 1.5G and 100 mW/cm2 simulated solar light from a Newport solar simulator system. During the photovoltaic measurements, all devices were masked with a mask to define the active area of 0.10 cm2. The photovoltage-time and photocurrent-time profiles during on-off cycles of illumination were measured using Autolab PGSTAT 302N electrochemical workstation. The incident photon to current conversion efficiency (IPCE) was measured using a Newport Optical Power Meter 2936-R controlled by TracQ Basic software.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 30.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: AgAl,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 240,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 22,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium (IV) isopropoxide (TTIP) and hydriodic acid (HI) were purchased from Aladdin, SnO2 colloidal dispersion (tin (IV) oxide, 15% in H2O colloidal dispersion) was purchased from Alfa Aesar, chlorobenzene and N,N-dimethyl-Formamide (DMF) were purchased from Youxuan Trade, and dimethyl sulfoxide (DMSO) was purchased from Bailinwei Trade, other anhydrous solvents were obtained from Alfa Aesar. Perovskite and HTL materials were obtained from Xi\\u2019an Polymer Light Technology Corp. All chemicals and reagents were used as received without any further purification.\\n\\nTiO2 precursor solution was prepared by a simple method reported by Christophe J. Barbe et\\u00a0al. []. TTIP (1.0\\u202fmL) was slowly added into HNO3 (6.0\\u202fmL, 0.1\\u202fmM) and HI (6.0\\u202fmL, 0.1\\u202fmM) respectively, heating and stirring at 80\\u202f\\u00b0C for 8\\u202fh. The solution was further filtered through a 0.45\\u202fmm PVDF syringe filter after falling to room temperature. SnO2 precursor was prepared by diluting the SnO2 colloidal with deionized water (volume ratio 1:5) and stirring for 12\\u202fh, followed by filtering through a 0.45\\u202fmm PVDF syringe filter.\\n\\nFluorine-doped tin oxide (FTO) glasses were ultrasonically cleaned in detergent solution, deionized water, ethyl alcohol and acetone for 30\\u202fmin respectively, then the glasses were transferred to the ultraviolet-ozone (UV\\u2013O3) cleaner for 15\\u202fmin. For double ETL, TiO2 film was prepared by spin-coating TiO2 or TiO2(HI) precursor solution at 3000\\u202frpm for 30\\u202fs, followed by annealing at 150\\u202f\\u00b0C for 1\\u202fh in air. SnO2 film was prepared by spin-coating SnO2 precursor solution on the TiO2 film at 3000\\u202frpm for 30\\u202fs, and then baked at 150\\u202f\\u00b0C for 2\\u202fh. For the deposition of Perovskite film, a normal one-step spin-coating method similar to a previous report was used []. CH3NH3I (1.0\\u202fM) and PbI2 (1.0\\u202fM) were dissolved in a co-solvent of DMF/DMSO (volume ratio 4:1) at room temperature and stirred for 12\\u202fh to form a perovskite precursor solution. This precursor solution was spin-coated on ETL at 3000\\u202frpm for 50\\u202fs and ethyl acetate was slowly dripped on the substrate 12\\u202fs after the beginning of spin-coating, then the film was annealed at 60\\u202f\\u00b0C for 5\\u202fmin and 100\\u202f\\u00b0C for 10\\u202fmin respectively. Spiro-OMeTAD was deposited after ETL cooling down, solution containing Spiro-OMeTAD (76.0\\u202fmg), 4-tert-butypyridine (28.5\\u202f\\u03bcL), Li-TFSI (17.5\\u202f\\u03bcL, 520\\u202fmg\\u202fmL\\u22121) and chlorobenzene (1.0\\u202fmL), deposited by spin-coating at 3000\\u202frpm for 30\\u202fs. Finally, about 60\\u202fnm thick Au counter electrode was deposited via vacuum thermal evaporation at rate of 1.0\\u202f\\u00c5\\u202fs\\u22121. The active area of PSCs was confirmed to be 0.09\\u202fcm2 by a non-reflective metal mask. All processes including fabrication, measurement and storage of devices with the structure of FTO/TiO2/SnO2/MAPbI3/Spiro-OMeTAD/Au were carried out under ambient conditions.\\n\\nFor analyzing crystal structure, X-ray diffraction (XRD) pattern was recorded on a Panalytical Empyrean X-ray diffractometer at a scan rate of 10\\u00b0 min\\u22121 with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.5406\\u202f\\u00c5). X-ray photoelectron spectroscopy (XPS, PerkinElmer, PHI 5400 ESCA system) analysis was used to calibrate binding energy value. For the observation of morphologies of nanoparticles and films, New Generation Cold Field Emission scanning electron microscopy (SEM, Hitachi, SU8000) and atomic force microscope (AFM, Bruber, Dimension Icon) have been used. Steady-state photoluminescence (PL) and time-resolved photoluminescence (TRPL) spectra were conducted on V2.7 fluorescence spectrometer from HORIBA. UV\\u2013visible (UV\\u2013vis) absorption spectroscopy surveys were performed on TU1901 spectrometer (Beijing Purkinje General Instrument Co., Ltd). The ultraviolet photoelectron spectroscopy (UPS, AXIS NOVA, Kratos Analytical Ltd, UK) using He I (21.2\\u202feV) as the photon source was employed to measure the work function. Photocurrent density-photovoltage (J-V) curves and open-circuit photovoltage decay (OCVD) of PSCs were measured with an electrochemical workstation (VersaSTAT 3, Ametek, USA) and a class ABB solar simulator (model 94021A, Newport, USA) under AM 1.5G sunlight (100\\u202fmW\\u202fcm\\u22122) illuminated with a sweep rate of 0.2\\u202fV\\u202fs\\u22121. The incident photon-to-electron conversion efciency (IPCE) was measured using the Crowntech solar cell quantum efciency measurement system (QTest Station 500AD, USA). Electrochemical impedance spectra (EIS) were measured on VersaSTAT 3 electrochemical workstation (Ametek, USA) with a frequency ranging from 0.1 to 106\\u202fHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60; 100,\\n Perovskite_deposition_thermal_annealing_time: 5.0; 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1400,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI) was purchased from Dyesol. Organic solvents including anhydrous N, N-dimethyl formamide (DMF), dimethyl sulfoxide (DMSO) and chlorobenzene (CB) were purchased from Sigma-Aldrich. Unless otherwise indicated, all materials were obtained from Xi'an Polymer Light Technology Corp. The PTAA (0.5\\u202fmg/mL) and NPB (2.5\\u202fmg/mL) were dissolved in chlorobenzene, and then mixed using desired ratios for NPB/PTAA ranging from 0.1, 0.5, 1.0, 1.5 to 3.0\\u202fwt%. Low NPB/PTAA doping ratios were obtained by diluting the high doping solution, and all mixed solutions were stirred and heated at 70\\u202f\\u00b0C overnight. The perovskite precursor solution contained 645\\u202fmg of PbI2 and 222\\u202fmg of CH3NH3I in a 1\\u202fmL of mixed solvent of DMSO and DMF (VDMSO/VDMF\\u202f=\\u202f1:4). In addition, 20\\u202fmg of PC61BM was dissolved in 1\\u202fmL of chlorobenzene. All solutions mentioned above were stirred at 60\\u202f\\u00b0C overnight and filtered with 0.45\\u202f\\u03bcm nylon filters before device fabrication.\\n\\nDevices were fabricated with a configuration of ITO/HTL/CH3NH3PbI3/PC61BM/Ag. ITO (15\\u202f\\u03a9/sq) glass substrates were cleaned sequentially with detergent, deionized water, acetone, and ethanol under sonication for 20\\u202fmin at 40\\u202f\\u00b0C. After drying, the substrates were further treated with ultraviolet-ozone for 15\\u202fmin. HTLs with different NPB doping ratios were fabricated by spin-coating at 4000\\u202frpm and 3000\\u202frpm for 35\\u202fs, followed annealing at 110\\u202f\\u00b0C for 10\\u202fmin. For the reference devices, the substrates with pristine PTAA were transferred out of the glovebox for a 10\\u202fs of oxygen plasma treatment and then transferred back into the glovebox for device fabrication. Note that because the bare PTAA film was so smooth and non-wetting towards DMF and DMSO, the precursor solution hardly coated the substrate, making it difficult to fabricate good quality of perovskite film with large grain size and less grain boundary on the top of it. CH3NH3PbI3 perovskite layers were then deposited using a one-step chlorobenzene-assisted solution process. The perovskite solution was added on top of the HTL and spin-coated at 6000\\u202frpm for 20\\u202fs. Then, 60\\u202f\\u03bcL of chlorobenzene was added dropwise at 6\\u202fs to form a transparent perovskite film. After 10\\u202fmin of annealing at 100\\u202f\\u00b0C on a hot plate, the perovskite film was obtained. After depositing the perovskite layer, a PC61BM electron transport layer was then deposited by spin coating at 2000\\u202frpm for 40\\u202fs, followed by annealing at 60\\u202f\\u00b0C for 10\\u202fmin. Finally, the samples were transferred to a vacuum chamber for evaporation of the silver electrodes, silver electrodes were finally deposited onto PC61BM under high vacuum through a shadow mask, defining a device area of 6.25\\u202fmm2.\\n\\nX-ray diffraction (XRD) data were collected using a Panalytical X'Pert Pro X-ray Powder Diffractometer with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f0.154\\u202fnm). The absorption spectra for the perovskite films were measured with a Varian 5E UV/Vis/NIR spectrophotometer. Scanning electron microscopy (SEM) was performed with field-emission electrons using a Nova 230 Nano SEM to obtain both top-view and cross-sectional images of films and devices. The contact angles of modified HTLs were measured using a JC000DI optical contact-measuring system (Zhong Chen. Shang Hai). The energy levels of different modified layers were measured by Ultraviolet Photoelectron Spectroscopy (UPS, Escalab 250Xi, Thermo Scientific). Photoluminescence (PL) measurements, including steady-state PL and time-resolved PL (TRPL) spectra for perovskite films deposited on different HTLs were collected using a Horiba Jobin-Yvon LabRAM HR800 with an excitation wavelength of 480\\u202fnm. Atomic Force Microscope (AFM) images were obtained using a Veeco Multimode V instrument to evaluate the surface morphology of films in tapping and intelligent modes.\\nThe current density-voltage characteristics of devices were measured at each 20\\u202fmV voltage step. And the measurement is simulated under Air-Mass (AM) 1.5 sunlight at 100\\u202fmW/cm2 (Newport, Class AAA solar simulator, 94023A-U) with a 2400 Series Source Meter (Keithley Instruments). The incident light intensity was varied from 100\\u202fmW/cm2 (1 Sun) to 1\\u202fmW/cm2 (0.01 Sun) and calibrated with an NREL certified KG5 filtered Si reference diode. External quantum efficiency (EQE) measurements were performed using a system combining a xenon lamp, monochromator, chopper, and lock-in amplifier and calibrated silicon photodetector. Long-term stability measurements were carried out for the best performing cells without encapsulation, the devices were kept in a dry room with controlled humidity (20%\\u202f<\\u202fRH<50%) and covered with aluminum foil during device storage. Electrical Impedance Spectroscopy (EIS) and Mott-Schottky capacitance analysis was carried out using an Ivium Electrochemical Workstation (Netherlands) under dark conditions. The dielectric spectra were tested using a Precision Impedance Analyzer (Agilent 4294A).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: NPB,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1500,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 0.065,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Initially, FTO on glass was removed for anode contact by etching the FTO with 30% HCl and zinc powder. Substrates were then cleaned with deionized water, acetone, and methanol and finally treated under oxygen plasma for 10 min to remove the organic residues. Nb-doped TiO2 target was prepared by cold pressing a mixture of TiO2 powder (purity: 99.999%, Alfa Aesar) and Nb2O5 powder (99.99%, Aladdin) and sintering at 1400 \\u2103 for 12 h in air. Nb-doped TiOx electron transport layer was deposited onto FTO/Glass or ITO/PET substrates (temperature 70oC) by PLD technique. The distance between the target and the substrate was approximately 55 mm. Prior to deposition, the chamber was evacuated to a pressure of ~4\\u00d710-6 mbar. Then, the deposition pressure of the chamber was controlled to be 0.20 mbar by pure O2 flow. The film thickness can be monitored by the film-thickness meter (RHEED) which was mounted on the substrate stage in the chamber. Then PbI2 powders were used to fabricate PbI2 films via thermal evaporation process (evaporation electric current: 50 A; evaporation voltage: ~220 V; Chamber pressure: ~8\\u00d710\\u2212 4 Pa). The PbI2 film thickness, which is detected by the film-thickness meter in the chamber, can be controlled by the evaporation time. Immersing the FTO/TiO2/PbI2 film in a solution of MAI in isopropanol (15 mg/mL) allows the formation of MAPbI3 through the reaction of PbI2 and MAI. The color of the film changed immediately from red-brown to dark brown, indicating the production of MAPbI3. When the reaction (40 min for full transformation) was finished, the devices were transferred into pure isopropanol solution to rinse off excess MAI and then kept 5 min at 50\\u201370 \\u2103 on hot plate for drying. After that, ZnPc hole modified layer was prepared on FTO/Nb-TiOX/MAPbI3 substrate by rotary vacuum thermal evaporation (320 \\u2103, 8\\u00d710\\u22124 Pa). Then another hole conductor was deposited on the FTO/TiO2/MAPbI3 or FTO/TiO2/MAPbI3/ZnPc substrate by spin coating spiro-OMeTAD at 1500 rpm for 30 s in nitrogen atmosphere and left in a closed dry box for 25 min. The spiro-OMeTAD solution was prepared by adding 100 mg of spiro-OMeTAD, 45 \\u00b5L of 4-tert-butylpyridine and 10 mg/m LiN(CF3SO2)2 N to 2 mL of chlorobenzene then stirred for 1 h. In order to ensure the consistency of the experimental process, the single Spiro-OMeTAD based devices in a mask was also placed in the chamber when the ZnPc based cells was put in the vacuum chamber to evaporate the compound (Dye content 97%, Sigma-Aldrich) at 320 \\u00baC. Finally, Au electrode with a thickness 100 nm was deposited on the top of HTM via thermal evaporation in a vacuum chamber (9\\u00d710\\u22124 Pa). An evaporation mask was used to define the areas of the devices, and the active area of each device was controlled to be 2\\u00d75, 5\\u00d75, 10\\u00d710 and 15\\u00d715 mm2.\\n\\nNon-masked devices were tested under a Class A solar simulator (ABET Sun 2000) at AM1.5 and 100 m/cm2 illumination conditions calibrated with a reference Silicon cell (RERA Solutions RR-1002), using a Keithley 2400 as a source-meter in ambient condition for J-V measurements with 60 points from +1.5 V to \\u22121.5 V. Incident photo-to-current conversion efficiency (IPCE) was recorded by using SolarCellScan100. The surface morphology of the films and cross-sections were characterized by a SIRION field-emission scanning electron microscope. XRD for Nb-TiOx films was carried out on a Rigaku D/max 2550 X-ray di\\ufb00ractometer, using a monochromatized Cu target radiation source at a scanning rate of 4o/minute. The EDS spectra were recorded on Nova_NanoSEM430. The local roughness of the thin films was characterized by atomic force microscopy (AFM; 5500, Agilent, Santa Clara, CA) operated in contact mode. The Hall Effect experiment was performed using the HL5500 Hall effect measurement system. Firstly, Nb doped TiOx films was deposited on the quartz glass substrate and formed a square (1 cm\\u00d71 cm) by the mask. The thickness of the Nb doped TiOx film was about 500 nm. Then, the In-Sn alloy was placed on the four corners of the square as the electrode. The Hall measurement revealed mobility of 0.02, 1.02 and 1.30 cm2 /(V s) for TiOx, 5% Nb doped TiOx and 10% Nb doped TiOx films. The absorption spectrum was recorded with UV\\u2013visible spectrophotometer (UV-1600). Water contact angles were measured by Dataphysics OCA20 contact angle measuring system in ambient air at room temperature for ZnPc/MAPbI3/FTO and spiro-OMeTAD/MAPbI3/FTO samples. Electrochemical impedance spectroscopy (EIS) were performed on a model CHI630E electrochemical analyzer (ChenHua Instruments Co. Ltd., Shanghai, China) in the frequency range of 0.1\\u2013105 Hz, and the applied bias voltage were set as 0 and 0.8 V, respectively.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Nb,\\n ETL_deposition_procedure: Pulsed laser deposition,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: none >> IPA,\\n Perovskite_deposition_procedure: Evaporation >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 30.0,\\n HTL_stack_sequence: ZnPc | Spiro-MeOTAD,\\n HTL_additives_compounds: Unknown | Li-TFSI; TBP,\\n HTL_deposition_procedure: Evaporation | Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 50,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 25,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials purchased for the fabrication of PSCs were used without further purification. PbI2 (99.999%) was purchased from Alfar Aesar. CH3NH3I (MAI) was synthesized in our lab according to a reported procedure. PCBM and Chlorobenzene (CB) were acquired from Sigma Aldrich.\\n\\nIn-situ graphene was synthesized at low temperatures via PATCVD with dc sputtering for Ti (10\\u202fnm)-buffer layer deposition. The Ti 10\\u202fnm buffer layer was deposited onto a cleaned PES substrate at 150\\u202f\\u00b0C via dc sputtering (DC power, 25\\u202fW; working pressure, 0.7\\u202fPa; gas flow rate of Ar/H2, 10/10 sccm (standard cc min\\u22121); deposition time, 10\\u202fmin; distance between target and substrate (T-S), 12\\u202fcm). After deposition of a Ti buffer layer, in-situ graphene was deposited onto the Ti buffer layer at 150\\u202f\\u00b0C via PATCVD under optimal conditions (RF power, 70\\u202fW; working pressure, 2.4\\u202f\\u00d7\\u202f102\\u202fPa; gas-flow rate of Ar/CH4/H2, 12/10/3 sccm; deposition time, 1.5\\u202fh; distance between plasma gun and substrate, 10\\u202fcm; distance between plasma guns, 10\\u202fcm) (See Fig. S1). The transfer graphene as a reference sample was prepared on copper foil via a CVD-growth process at 950\\u202f\\u00b0C. PMMA (poly methyl methacrylate) was spin-coated onto the graphene/copper foil and baked at 180\\u202f\\u00b0C for 2\\u202fmin. The copper foil was then etched using an aqueous solution of FeCl3 at 40\\u202f\\u00b0C. Finally, the PMMA/graphene was transferred onto the cleaned PES. The substrate was submerged in an acetone solution to remove the PMMA. The samples were then dried in a nitrogen glove box.\\n\\nFlexible PSC devices with a planar structure consisting of AAA/PCBM/MAPbI3/NiOx/Graphene/PES substrate were fabricated to investigate the influence of perovskite thickness on device performance. First, a conductive area was covered by a tape at the edge of the Graphene/PES substrate (graphene sheet resistance: ~81\\u202f\\u03a9/\\u25a1) to allow a measurement connection. Next, an electron-blocking layer (NiOx) with a thickness of 10\\u202fnm was deposited via facing target sputtering (FTS) onto the graphene electrode that served as a hole transport layer. The FTS was designed to prevent the plasma-damage of the graphene for deposition of NiOx blocking layer onto the graphene film. The FTS technique was previously described [] for an ultrathin, compact NiOx blocking layer whereby two NiO targets (99.99%) were placed in opposition at a distance of 9\\u202fcm with plasma filling the space between the surfaces of the targets, and an RF power of 100\\u202fW was applied from a gun that created an Ar:O2 gas-flow rate of 10:1 sccm with the working pressure maintained at 0.2\\u202fPa. The substrate holder was heated using a halogen lamp at 100\\u202f\\u00b0C placed in a horizontal direction far from the targets at equal distances of 9\\u202fcm. A 10\\u202fnm thickness of NiOx was obtained after an appropriate deposition time of 9\\u202fmin.\\nA smooth and dense perovskite (MAPbI3) films with a thickness of ~300\\u202fnm were synthesized using a one-step process via chemical vapor deposition (CVD). The schematics of CVD are mentioned in our previous work [], whereby a 2-inch quartz tube furnace (KJMTI OTF1200X) was used with two separate temperature zones. For the present study, the perovskite materials were simultaneously fabricated through dual-source evaporation from PbI2 and MAI (Sigma Aldrich) using argon as a carrier gas. Then, 300\\u202fmg of MAI and 150\\u202fmg of PbI2 were placed in the upper-flow right zone (zone 1) to confine the vapor. According to the differences in the melting-point temperatures of the PbI2 and MAI powder, the positions of these sources were located at the center and 10\\u202fcm to the right side of zone 1, respectively. The bl-NiOx/Graphene substrates were placed in the down-flow on the left side of zone 2 and set at a temperature of 100\\u202f\\u00b0C. The furnace was then sealed and pumped down to a pressure of 1.3\\u202f\\u00d7\\u202f102\\u202fPa under the control of Ar gas flow at 100 sccm. The perovskite layers were optimized for high crystallinity without PbI2 or MAI phases by varying different key parameters such as the gas flow rate, temperature, time, and the amounts of two different sources. After fabrication of the perovskite layer, an in-situ annealing process was performed in the second zone of the furnace immediately after deposition at 100\\u202f\\u00b0C for 60\\u202fmin.\\nFor the electron transport layer, a 40\\u202f\\u03bcl solution of PCBM dissolved in chlorobenzene (25\\u202fmg/ml) was spin-coated onto MAPbI3/bl-NiOx/graphene/PES substrates at 4000\\u202frpm for 10\\u202fs, then dried at 80\\u202f\\u00b0C for 15\\u202fmin to allow the PCBM to crystallize and diffuse into the perovskite layer. Finally, devices were completed with the deposition of an AAA top electrode via FTS []. The AZO targets (3% Al doping) were used with target-to-target and target-to-substrate distances of 9 and 10\\u202fcm, respectively. Initially, the sputtering chamber was evacuated to a base pressure of 1.3\\u202f\\u00d7\\u202f10\\u22124\\u202fPa using a turbo molecular pump. RF power of 100\\u202fW was used for each gun for an Ar flow rate of 10 sccm and a working pressure that was maintained at 0.4\\u202fPa. The Ag layer was deposited at a pressure of 0.4\\u202fPa with dc power of 6.5\\u202fW.\\n\\nOptical transmittance values for the PES/graphene and full device were measured using S-3100 UV\\u2013vis spectroscopy. The resistivity, Hall mobility, and carrier density were measured using a Z-theta method within a range of from 100\\u202fHz to 10\\u202fMHz with an impedance/gain-phase analyzer (HP4194A) that also was used to measure the Hall effect of the van der Pauw geometry (HL-5500PC, Accent). The surface morphologies of the perovskite dye and the cross-sectional images of the solar cell devices were analyzed using scanning electron microscopy (SEM) (TOPCON DS-130C). The root-mean-square (rms) roughness of MAPbI3 and PCBM/MAPbI3 were measured via atomic force microscopy (AFM). The UPS ((ultraviolet photoelectron spectroscopy) spectra for determination of work-function of the graphene electrodes were measured using an Axis-Nova (Kratos) with a He discharge lamp. Photocurrent-voltage (I\\u2013V) characteristics of the solar cells were measured using an IVIUMSTAT under illumination from a Sun 3000 solar simulator composed of 1000\\u202fW mercury-based Xe arc lamps and AM 1.5-G filters. The external quantum efficiency (EQE) spectra of PSCs were measured in air conditions by a Zolix Solar Cell Scan 100 system equipped with a 100\\u202fmW Xenon lamp. Light intensity was calibrated with a silicon photodiode. The bending test was performed within a calculated strain percentage. In these tests, a sample size of 1\\u202f\\u00d7\\u202f1\\u202fcm2 was fixed in a bent stage using gas vents with a setup delay time of 1\\u202fs for each cycle. The current-voltage J-V curves of the solar devices were measured after the bending test at the same time and under the same conditions.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: PES | Ti | Graphene,\\n ETL_stack_sequence: NiO-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Sputtering,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: none,\\n Perovskite_deposition_procedure: CVD,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: PCBM-60,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: AZO | Ag | AZO,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Sputtering | Sputtering | Sputtering,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: 500,\\n Stability_PCE_initial_value: 11.7,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The NiOX powder was prepared according to the published literature []. Devices were arranged on conductive indium\\u2013tin oxide (ITO)-coated glass substrates, which were extensively cleaned by deionized water, acetone, and isopropanol. The device architecture is ITO/NiOX/MAPbI3/PCBM/ZrAcac/Au. The NiOX NCs ink (20\\u202fmg/mL in DI water) was spin-coated onto the clean surface of the ITO substrates at 2000\\u202frpm for 60\\u202fs in air to obtain approximately 40\\u202fnm NiOX film. The MAPbI3 precursor solution was prepared in a glovebox from a 1.1M:1.1M ratio of PbI2:MAI in a mixture solution of DMF, \\u03b3-butyrolactone (GBL), and dimethyl sulfoxide (DMSO) with a volume ratio of DMF/DMSO/GBL of 5:2.5:2.5, The spin-coating procedure was performed at 1500\\u202frpm for 15\\u202fs, followed by 3000\\u202frpm for 35\\u202fs. At 5\\u202fs before the end of the spin-coating, a C60 solution (2\\u202fmg/mL) from toluene was pipetted onto the substrate. Perovskite precursor-coated substrate was annealed first at 70\\u202f\\u00b0C for 3\\u202fmin and then at 100\\u202f\\u00b0C for 7\\u202fmin to form the perovskite film. Subsequently, the ETL layer of PCBM (20\\u202fmg/mL in dichlorobenzene) was initially spin-coated on perovskite film at the rate of 1000\\u202frpm for 60\\u202fs and then at 4000\\u202frpm for 60\\u202fs. A ZrAcac (2\\u202fmg/mL in absolute alcohol) buffer layer was then deposited by spin coating at 4000\\u202frpm for 40\\u202fs. Finally, the samples were moved to a thermal evaporator for Au (approximately 100\\u202fnm) deposition. The active area of the device is 0.04\\u202fcm2. The thickness of the perovskite is approximately 350\\u202fnm and that of PCBM is approximately 30\\u202fnm. Meanwhile, the thicknesses are approximately 4\\u202fnm for ZrAcac. Encapsulation: In the glove box filled with nitrogen, the device is covered with a glass sheet at the back and then sealed with a Torr Seal epoxy.\\n\\nThe J\\u2013V characteristics were measured using a Keithley2635B source meter. Illumination was provided by an Abet 2000 solar simulator with AM1.5G spectra at 100\\u202fmW/cm2. Film thickness was checked with an Ambios XP-2 profilometer. The external quantum efficiencies (EQEs) data were recorded using a Zolix Solar Cell Scan 100 with a calibrated silicon reference cell, and these measurements were converted to EQE. The UV\\u2013vis absorption spectra of active layers were acquired by a Shimadzu UV-3101\\u202fPC spectrophotometer. Scanning electron microscope (SEM) measurements were performed using a Hitachi. X-ray diffraction (XRD) spectra were performed on a D/max 2200 v X-ray powder diffractometer equipped with Cu-K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.540\\u202f\\u00c5). The morphology and phase images of active layers were performed by using atomic force microscopy (AFM) in tapping mode with the scan size of 5\\u202f\\u00d7\\u202f5\\u202f\\u03bcm [] or 10\\u202f\\u00d7\\u202f10\\u202f\\u03bcm [] by SPI3800/SPA400. The measured ionization potentials (photoelectron emission spectrum) were measured by AC-2. TRPL and PL spectra were calculated by Delta flex and Nanolog FL3-2Ihr, respectively. XPS was tested through Axis Ultra. The light source for the stability test is a LED lamp (color temperature 5000\\u202f\\u00b0C), which has stable light intensity equivalent to one sun illumination. We use the Source-Meter Keithley 2635 to measure the J\\u2013V characteristics of the PSCs.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Zr(acac)4,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: C60,\\n Perovskite_deposition_solvents: DMF; DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70; 100,\\n Perovskite_deposition_thermal_annealing_time: 3.0; 7.0,\\n HTL_stack_sequence: NiO-np,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The inverted MAPbI3 PSCs with p-i-n type junction were fabricated based on the structure of ITO/PTAA/MAPbI3/PCBM/Bphen/Cu. Shown in Fig. 1 are the fabrication scheme of PSCs and the experimental schematic diagram. The ITO substrates were cleaned according to a standardization process. Then they were further treated with UV-ozone for 10\\u202fmin after drying in a N2 flow and finally transferred into a N2-filled glovebox. The PTAA layer was spin-coated on ITO surface as hole transport layer following the procedure reported previously []. The MAPbI3 film was deposited on the PTAA layer using the standard antisolvent method with anhydrous chlorobenzene (CB) as the antisolvent as reported by Xiao et al. []. The mixture of PbI2 and MAI was dissolved in a mixed solvent of N,N-dimethylformamide (DMF): dimethyl sulfoxide (DMSO) before it was spun onto PTAA at 5000\\u202fr.p.m. Subsequently, the MAPbI3 sample was quickly washed with CB and then annealed at 100\\u202f\\u00b0C for 20\\u202fmin. The PCBM solution (20\\u202fmg/mL in CB) was spin-coated onto the perovskite substrate at 1500\\u202fr.p.m. for 10\\u202fs and 3500\\u202fr.p.m. for 35\\u202fs, then annealed at 100\\u202f\\u00b0C for 30\\u202fmin. Finally, the devices were finished by thermally evaporating Bphen (\\u223c15\\u202fnm) and copper (\\u223c70\\u202fnm) in sequential order.\\nTo evaluate the light-induced degradation effect, the as-grown devices were put into a glove-box with both a humidity level and an oxygen level below 0.1\\u202fppm and then were aged using a LED lamp with an illumination intensity of 200\\u202fmW/cm2 at temperature ranging between 25 and 35\\u00a0\\u00b0C. To accelerate the aging process, the devices were set in short circuited states by directly connecting the anode to the cathode when they were exposed to the illumination for different time duration. Then, current density\\u2212voltage (J\\u2212V) characteristics of PSCs were measured by a Digital Source Meter (Keithley, model 2420) at 300\\u00a0mV/s from \\u22121.5\\u00a0V to +1.5\\u00a0V, and the standard silicon solar cell was employed to calibrate the solar simulator (Newport 91160s, AM 1.5G) with a light intensity of 100\\u00a0mW/cm2. Furthermore, the upper layers of the PSCs were peeled off to expose the MAPbI3 layer for further characterization, where the Cu electrode was removed using adhesive tape and the electron transport layers of Bphen and PCBM were washed off with CB. The crystallographic properties and the surface morphology of the MAPbI3 films were characterized by employing an X-ray diffractometer (XRD, Rigaku D, Max 2500) and an atomic force microscope (AFM, Agilent Technologies 5500AFM/SPM System), respectively [,]. Ultraviolet photoelectron spectroscopy (UPS, He I, 21.22\\u202feV) and X-ray photoelectron spectroscopy (XPS, Al K\\u03b1 X-ray source, 1486.6\\u202feV) were employed to investigate the detailed exposure effects of the devices [].\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Bphen,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Cu,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 35.0; 35.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 13,\\n Stability_PCE_initial_value: 15.2,\\n Stability_PCE_end_of_experiment: 48,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All used reagents were purchased from Sigma-Aldrich Corp, unless specifically mentioned. PC61BM (99.5%) was supplied by Luminescence Technology Corp, Taiwan, China. BCP and methylammonium iodide (MAI) were supplied by Xi'an Polymer Light Technology Corp, China. PEDOT:PSS (P VP AI 4083) was bought from Clevios Corp. FTO glasses with sheet resistance of 15\\u202f\\u03a9\\u202f\\u25a1\\u22121 were purchased from Nippon Glass Corp (Japan) and used as substrates for preparing PSCs.\\n\\nNiO NCs were synthesized by a solvothermal method. Firstly, a solution containing 0.257\\u202fg nickel (II) acetylacetonate, 6\\u202fmL OAm and 10\\u202fmL toluene was prepared. Secondly, the solution was poured into a 50\\u202fmL autoclave and heated at 180\\u202f\\u00b0C for 24\\u202fh. After natural cooling to room temperature, the solution was poured out and mixed with 20\\u202fmL ethanol to precipitate NiO NCs. The NiO NCs were collected after being centrifuged at a rate of 12,000\\u202frpm for 10\\u202fmin and then re-dispersed in toluene with concentration of 10\\u202fmg\\u202fmL\\u22121.\\nFTOs (1.5\\u202f\\u00d7\\u202f1.5\\u202fcm2) were etched by Zn powder and 2\\u202fM HCl solution to form the designed pattern and then consecutively washed with isopropanol, acetone, distilled water and ethanol. Before preparing inverted planar PSCs, these FTOs were treated with UV-ozone for 30\\u202fmin. The as-prepared NiO NCs dispersed in toluene (10\\u202fmg\\u202fmL\\u22121) was used for preparing NiO HTLs on the patterned FTOs by spin-coating the dispersion at 4000\\u202frpm for 30\\u202fs, soon afterwards heated at 500\\u202f\\u00b0C for 30\\u202fmin. For comparison, the PEDOT:PSS HTL was also prepared on the patterned FTO. The PEDOT:PSS solution was spin-coated on the patterned FTO at 4000\\u202frpm for 30\\u202fs and dried at 150\\u202f\\u00b0C for 10\\u202fmin to form 40\\u202fnm thick PEDOT:PSS HTL (Kim et al., 2017). The thickness of the NiO NCs and PEDOT:PSS films were identified by the cross-sectional SEM images.\\nMAPbI3 perovskite layers were deposited on the NiO and PEDOT:PSS HTLs with the typical anti-solvent methodology (Ahn et al., 2015). A 1.2\\u202fmol\\u202fL\\u22121 MAPbI3 precursor solution made of 1.66\\u202fg PbI2, 0.58\\u202fg MAI, 500\\u202f\\u03bcL dimethylsulfoxide and 2500\\u202f\\u03bcL N,N-dimethylformamide was prepared firstly. Then, 80\\u202f\\u03bcL precursor solution was dripped on top of the NiO or PEDOT:PSS HTL and spin-coated at 1000\\u202frpm for 10\\u202fs and then at 6500\\u202frpm for 20\\u202fs. When the second-step spin-coating at 6500\\u202frpm lasted for 5\\u202fs, the anti-solvent of chlorobenzene (500\\u202f\\u03bcL) was dripped on the rotating substrate to rinse out residual DMSO and DMF in the precursor film. After thermal treatment at 100\\u202f\\u00b0C for 10\\u202fmin, the crystalline MAPbI3 perovskite layer was formed. A thin layer of PC61BM was spin-coated onto the MAPbI3 perovskite layer from a 20\\u202fmg\\u202fmL\\u22121 chlorobenzene solution at 1500\\u202frpm for 45\\u202fs and dried at 70\\u202f\\u00b0C for 10\\u202fmin. After that, 100\\u202f\\u03bcL saturated methanol solution of BCP was dripped on top of the PC61BM layer during spin-coating at 6000 rmp and then dried at 70\\u202f\\u00b0C for 10\\u202fmin again. Finally, an Au electrode about 100\\u202fnm was thermally evaporated on the BCP layer under high vacuum through a shadow mask.\\n\\nThe morphologies were observed by a JEM-2100 transmission electron microscopy (TEM) and a SU8000 field-emission scanning electron microscopy (SEM). The X-ray diffraction (XRD) patterns were recorded with a Bruker D8 Advance X-ray diffractometer using Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.5418\\u202f\\u00c5). The transmittance spectra were measured by a Lamda 950 UV\\u2013Vis-NIR spectrophotometer. The steady-state photoluminescence (PL) spectra were acquired using a fluorescence spectrophotometer (Thermo Scientific Lumina). The time-resolved photoluminescence (TRPL) spectra were acquired using an Omin-\\u03bb Monochromator/Spectrograph with the time-correlated single-photon counting method (Zolix).\\nThe photovoltaic performance of PSCs were evaluated by the current density-voltage (J-V) characteristic curves, incident-photo-to-current conversion efficiency (IPCE) curves, stabilized current density and power output curves. Namely, the J-V curves of PSCs were recorded with a computer-controlled Keithley 2400 source meter under simulated AM 1.5 G solar illumination at 100\\u202fmW\\u202fcm\\u22122 with #94043A solar simulator (PVIV-94043A, Newport, USA) in air. The voltage step and delay time were 20\\u202fmV and 10\\u202fms, respectively. The forward and reverse scans started from \\u22120.1\\u202fV to 1.2\\u202fV and 1.2\\u202fV to \\u22120.1\\u202fV, respectively. The stabilized current density and power output curves were recorded close to the maximum power point, which was extracted from the J-V curves. The IPCE curves were measured as a function of wavelength from 300\\u202fnm to 850\\u202fnm using the Newport IPCE system (Newport, USA). The PSCs with the active area of 0.12\\u202fcm2 (0.3\\u202f\\u00d7\\u202f0.4\\u202fcm2) and without any encapsulation were prepared for measurements. The electrochemical impedance spectroscopy (EIS) measurements were conducted on a Zennium electrochemical workstation (IM6) in dark conditions with the frequencies from 100\\u202fmHz to 2\\u202fM\\u202fHz, the bias of 0\\u202fV and the amplitude of 20\\u202fmV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 96,\\n Stability_PCE_initial_value: 10.69,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A fluorine-doped tin oxide-coated glass substrate (FTO, Dyesol TEC 15) was etched with Zn powder and HCl diluted in deionized water. The FTO substrate was then cleaned by ultrasonication in acetone, deionized water, and ethanol. A compact layer of TiO2 was deposited onto the FTO by spin coating using 0.3\\u202fM titanium diisopropoxide bis(acetylacetonate) solution in 1-butanol at 500\\u202f\\u00b0C. A mesoporous TiO2 (particle size\\u202f\\u223c\\u202f20\\u202fnm) film was then spin-coated onto the compact layer TiO2/FTO using TiO2 paste (Dyesol, DSL 18NRT) diluted in ethanol (1:4, weight ratio) and annealed at 500\\u202f\\u00b0C for 30\\u202fmin. The substrate was treated with 0.04\\u202fM aqueous TiCl4 for 30\\u202fmin at 70\\u202f\\u00b0C, rinsed with methanol, and dried at 500\\u202f\\u00b0C for 30\\u202fmin. MAI (Lumtec) and SnI2 (Alfa Aesar) powders were used to prepare 40\\u202fwt% MASnI3 solution and stirred in a different ratio mixture of DMF and DMSO (v:v) at 70\\u202f\\u00b0C for 12\\u202fh. The substrate was moved to a glovebox for perovskite material deposition and 40\\u202fwt% solutions of MASn(I1\\u2212xBrx)3 with different halide mixing ratios were made by reacting MAI, MABr (Lumtec), SnI2, and SnBr2 (Aldrich) in DMF/DMSO (4:1, v:v) at 70\\u202f\\u00b0C for 12\\u202fh. The resulting solution was filtered before use and coated on a mesoporous-TiO2/compact-TiO2/FTO substrate at 4500\\u202frpm for 45\\u202fs. The samples were then annealed on a hot plate at 100\\u202f\\u00b0C for 10\\u202fmin. Subsequently, 25\\u202f\\u03bcl of a hole transport layer (HTM) was deposited using a spin coater at 2500\\u202frpm for 45\\u202fs. The HTM mixture consisted of 80\\u202fmg of 2,20,7,70-tetrakis(N,N-di-pmethoxyphenyl-amine)-9,90-spirobifluorene (spiro-MeOTAD), 8.4\\u202fml of 2,6-lutidine, and 51.6\\u202fml of bis (trifluoromethane) sulfonamide lithium salt (Li-TFSI) solution (154\\u202fmg\\u202fml\\u22121 in acetonitrile) dissolved in 1\\u202fml of chlorobenzene. Finally, a top electrode of Au was deposited by thermal evaporation.\\n\\nThe current density-voltage (J-V) characteristics of these devices were measured using a computer-controlled Keithley 4200SCS over a voltage scan range of \\u22120.5 to 1.5\\u202fV, voltage step of 10\\u202fmV, and delay time of 1\\u202fms. An Oriel Sol3A Class AAA Solar Simulator (model, Newport 94023A) equipped with a 450\\u202fW xenon lamp and an air mass (AM) 1.5 filter was used as the light source. Light intensity was calibrated to 100\\u202fmW\\u202fcm\\u22122 using a Newport Oriel 91150V reference cell. The active area of the device was 0.06\\u202fcm2.\\nWe also investigated the surface morphology of the perovskite layer using scanning electron microscopy (SEM) and elemental mapping via energy-dispersive X-ray spectroscopy (EDS) (FE-SEM, JEOL, JSM-6700F). The optical properties of the perovskite thin films were analyzed using an ultraviolet\\u2013visible (UV\\u2013VIS) absorption spectrometer (PerkinElmer, Lambda 750). To examine the work function and valence band maximum (VBM) of the series of tin-based perovskites, ultraviolet photoemission spectroscopy (UPS) measurements were conducted using a SPECS PHOIBOS 150 hemi-spherical analyzer. For UPS measurement, an ultraviolet discharge lamp was used as an excitation source (He I, 21.22\\u202feV) and a sample bias of \\u221210\\u202fV was applied to obtain the SEC in normal emission geometry. SEM and UPS measurements were performed immediately after they were taken out the glove box and placed in a SEM and UPS vacuum chambers.\\nRaman spectra were measured using a spectrometer (Model 207, McPherson Inc.) equipped with a nitrogen-cooled charge-couple device array detector. Samples were measured using an excitation laser with a wavelength of 632.8\\u202fnm (He-Ne laser) and a spot size of 1\\u202f\\u00b5m at a power of 8.6 mW. Raman measurement was performed immediately with the time of scanning \\u223c49\\u202fs.\\nThe topography and local current were measured using a commercial AFM (Nanofocus Inc., n-Tracer) equipped with a Pt/Ir-coated silicon cantilever (Nanosensor) under an inert atmosphere of nitrogen gas. A voltage bias was applied between the tip and the FTO substrate and a conductive probe was scanned across the sample in contact mode. External sample bias was swept at +1\\u202fV. The tip was grounded and the current was detected with a single terminal.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MASnI3,\\n Perovskite_composition_short_form: MASnI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 3.33,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Most chemicals such as lead iodide (PbI2), anhydrous N,N-dimethylformamide (DMF) and anhydrous 2-propanol (IPA) were purchased from Sigma-Aldrich and used as received. Poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS, Al4083) and CH3NH3I were purchased from Clevios and Lumtec, respectively.\\n\\nITO glasses were cleaned with deionized water, acetone and ethanol for 15 minutes each and then dried in an oven. Before device fabrication, the ITO glasses were treated in a UV ozone cleaner for 20 min. Afterward, the PEDOT:PSS layer was deposited onto the ITO surface by spin-coating at a spin speed of 4000 rpm for 40 s, and then annealed at 150 \\u00b0C for 15 minutes in air. The perovskite film was deposited by a two-step spin-coating method with different MAI loading times as reported in our previous work. First, the PbI2 solution (462 mg mL\\u22121 in DMF) was coated on the top of the PEDOT:PSS layer at 4000 rpm for 40 s and dried at 70 \\u00b0C for 10 minutes. Then the CH3NH3I solution (35 mg mL\\u22121 in IPA) was dropped onto the PbI2 film and allowed to stand for different times from 0 s to 180 s and then spin-coated at 4000 rpm for 40 s. Subsequently, the perovskite films were covered with a Petri dish on a hot plate and 15 \\u03bcL DMF solvent was added at the edge of the Petri dish for solvent annealing at 100 \\u00b0C for 1 hour. Finally, fullerene C60 (20 nm), 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP: 5 nm) and an Au electrode (80 nm) were deposited onto the perovskite films by thermal evaporation. The deposition and annealing processes of perovskite films were sequentially performed inside a nitrogen filled glovebox. The active area of the solar cell was 0.1 cm2.\\n\\nThe X-ray diffraction (XRD) patterns were obtained on a D2 Phaser instrument using Cu K\\u03b1 (\\u03bb = 0.154 nm) radiation to investigate the composition profile of perovskite films prepared with different MAI loading times. For the samples after shelf-life tests, the Au electrodes were peeled off from the devices with tapes (see the photographs in the ESI, Fig. S4\\u2020). Scanning electron microscopy (SEM, Philips XL30 FEG) was employed to characterize the morphology of perovskite films.\\nThe current\\u2013voltage (J\\u2013V) curves were recorded using a Keithley 2400 source meter under AM1.5G illumination at 100 mW cm\\u22122. To evaluate the recombination process in perovskite solar cells, light intensity dependent J\\u2013V characteristics were studied at a scan rate of 200 mV s\\u22121 under the illumination with various light intensities ranging from 100 mW cm\\u22122 to 1.4 mW cm\\u22122. In order to identify the mobile ion concentration in the perovskite film, transient ionic current was employed. An external forward bias (at the Voc point) was applied to the devices for 1 minute without illumination, followed by releasing the voltage to 0 V and recording the current as a function of time for another 60 s. All the measurements were performed under dark conditions. For the stability measurements, all the devices were stored inside a dry box with humidity around 40\\u201350% under ambient light. And the devices were taken out to complete the J\\u2013V characteristics at set intervals. The shelf-life of perovskite solar cells studied in this work was defined as the time when the efficiencies dropped to 70% of the initial value. For the photothermal deflection spectroscopy (PDS) measurements, perovskite films with different MAI loading times were deposited on quartz substrates. Monochromatic light chopped at 13 Hz as the pump beam was applied to shine onto the samples. Meanwhile, a probe laser was placed on the perpendicular side and a position sensitive sensor connected with a lock-in amplifier (Stanford Research, Model SR830) is placed on the opposite side to detect the deflection signals. For the transient photocurrent measurements, the devices were connected to a 50 \\u03a9 input terminal. A laser pulse (532 nm and 6 ns) was applied to perturb the devices.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> 60.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 400,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 40,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"To prepare the perovskite precursor solution, MAI (methylammonium iodide, HeptaChroma) and PbI2 (Sigma) powder were mixed in anhydrous DMF (dimethylformamide, Aladdin):NMP (N-methyl pyrrolidone, Aladdin) (3:2) with a molar ratio of 1:1. The solutions were stirred overnight at 70 \\u00b0C and filtered with 0.45 \\u03bcm PVDF filters before device fabrication. TAPC was purchased from Heraeus, Germany. Bathocuproine (BCP) was purchased from Luminescence Technology Co. and the phenyl-C61-butyric acid methyl ester (PC61BM) was purchased from Solarmer Materials Inc. Bathophenanthroline (Bphen) (99%) was received from Xi'an Polymer Light Technology Co. Cs2CO3 (99.995%) was purchased from Sigma-Aldrich.\\n\\nDevices were fabricated with the structure ITO/TAPC/CH3NH3PbI3/PC61BM/IML/Ag. The patterned ITO glass substrates (10 \\u03a9 \\u25a1\\u22121) were cleaned by sequential sonication in detergent, deionized water, acetone, isopropanol and anhydrous alcohol for 15 min at each step. Then the precleaned ITO substrates were exposed to Ultraviolet-Ozone (UVO) irradiation for 20 min. TAPC solution (10 mg ml\\u22121 in chlorobenzene) was spin-coated onto the ITO substrates at 4000 rpm for 40 s and then annealed at 120 \\u00b0C for 20 min. Subsequently, the perovskite precursor solution of CH3NH3I and PbI2 was deposited onto TAPC/ITO substrates by a consecutive two-step spin-coating process at 1000 rpm and at 4000 rpm for 5 and 30 s, respectively. At the final spin-stage, toluene as an anti-solvent was dripped onto the substrate. After this the perovskite-precursor coated substrate was annealed at 105 \\u00b0C for 10 min. Afterward, the PC61BM (20 mg ml\\u22121 in chlorobenzene) was deposited by spin-coating at 1500 rpm for 30 s. The IMLs (BCP, Bphen:20wt%Cs2CO3, and Bphen:20wt%Cs2CO3:10wt%BCP) with 0.5 mg ml\\u22121 in ethanol was spin-coated at 3000 rpm for 30 s without further annealing. Finally, the Ag metal electrode was deposited by thermal evaporation through a shadow mask which determined the cell area to be 10 mm2 at a pressure of ca. 3 \\u00d7 10\\u22124 Pa.\\n\\nThe current density\\u2013voltage characteristics (J\\u2013V) were measured inside a N2-glovebox using a Keithley 2400 source-meter under the illumination of AM 1.5G (100 mW cm\\u22122). Similarly, the EQE measurements were performed using a CrownTech quantum efficiency measurement system (QTesT 1000ADX) in air. Likewise, absorption spectra were recorded on a UV-vis spectrophotometer (Hitachi, U-3900H). The variation of the morphology was characterized using an atomic force microscope (AFM, Bruker, MultiMode 8). Photoluminescence (PL) spectra were determined using a fluorescence spectrofluorometer (F-7000, Hitachi). Electrochemical impedance spectroscopy (EIS) was performed with an electrochemical workstation (CHI660E, Chenhua Co. Ltd, Shanghai). The HOMO level was measured by ultraviolet photoemission spectroscopy (UPS, AXIS Ultra, DLD Kratos). Time-resolved PL was measured using an FLS920 (Edinburgh Instruments) fluorescence spectrometer.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCB,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; NMP,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 105,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: TAPC,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 200,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals and reagents were employed as received from chemical companies without any further purification. P3CT-Na was synthesized through the reaction of poly[3-(4-carboxylbutyl)thiophene] (P3CT, Mw: 30\\u201340 K, Rieke Metals) with sodium hydroxide (NaOH, molar ratio 1:1.025) in H2O at 60 \\u00b0C under stirring. Polyaspartic acid sodium water solution (PASP, 40 wt%) from Maya-R company (China). Before use, PH was adjusted to 7 with glacial acetic acid and diluted with deionized water to 1, 0.5, 0.1, 0.05, and 0.01 mg mL\\u22121 and other purity. PC61BM, BCP, and C60 were purchased from Lumtec (Taiwan).\\n\\nThe ITO/glass substrate was cleaned by successive sonication in detergent, deionized water, acetone and isopropyl alcohol, and then dried by using a nitrogen flow. Then the ITO substrates were treated with O2-plasma for 15 min. P3CT-Na was spin-coated on ITO at 4000 rpm for 60 s. After thermal annealing at 140 \\u00b0C for 20 min in air, PASP (0.1 mg mL\\u22121) was spin-coated on P3CT-Na at 4000 rpm for 30 s. After thermal annealing at 140 \\u00b0C for 20 min in air, the substrates were transferred into a glove box filled with N2. The perovskite precursor solution was prepared by dissolving CH3NH3I and PbI2 (1:1, 1.40 M) in 1 mL mixed solvent of DMF and DMSO (volume ratio 4:1). Perovskite films were fabricated using an anti-solvent method at 400 rpm 3 s and 4800 rpm 30 s. And the anti-solvent chlorobenzene (CB, 200 \\u03bcL) was added onto the substrate 14 s after the spin-coating started. Then the substrate was put on a hotplate at 75 \\u00b0C for 2 min and 90 \\u00b0C for 4 min to form perovskite films. After the substrate cooled to room-temperature, PCBM solution (12.5 mg mL\\u22121 in CB) was spin-coated on the perovskite films at 400 rpm for 3 s and 4800 rpm for 30 s. Then the substrate was transferred to a vacuum chamber. 20 nm C60, 8 nm BCP and 100 nm Ag were deposited by thermal evaporation using a metal shadow mask. The device area was 4 mm2.\\n\\nThe current-density versus voltage (J\\u2013V) characteristics of MAPbI3 solar cells and single carrier devices were recorded by using a Keithley 2400 Source Meter under a nitrogen environment. MAPbI3 solar cells were tested under irradiation by using a solar simulator calibrated with a standard Si cell or and single carrier devices were tested in the dark. The irradiation intensity was adjusted by using an optical wheel filter and determined according to the current reading of the calibration cell. The incident photon to current efficiency (IPCE) of CH3NH3PbI3 solar cells was measured by using a Newport external quantum measurement system (Model 66920). Impedance spectroscopy of CH3NH3PbI3 solar cells was performed by using a potentiostat under a nitrogen environment and the data were analysed by using the ZView 2 program. Different intensities of sunlight were simulated with filters of different transmittances.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 75; 90,\\n Perovskite_deposition_thermal_annealing_time: 2.0; 4.0,\\n HTL_stack_sequence: P3CT-Na,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 4200,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 84,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemical reagents were purchased from Sigma-Aldrich and used as received without further purification.\\n\\nFluorine-doped tin oxide (FTO) coated glass (Pilkington TEC 15, 15 \\u03a9 per square) was etched using 0.1 M HCl solution diluted in Milli-Q water without Zn powder. The etched substrates were cleaned with 2% hellmanex diluted in the Milli-Q water, rinsed with Milli-Q water/ethanol, and then dried with clean air. A p-type NiMgLiO compact layer (\\u223c20 nm thick) was then deposited on the FTO glass using spray pyrolysis according to our previous work. The anti-solvent method was used for the perovskite layer deposition: an 80 \\u03bcL DMF/DMSO (4:1 by volume) solution of PbI2/MAI (1.05:1 by molar ratio, with a concentration of 1.5 M) was spin-coated at a rotation speed of 5000 rpm for 30 seconds, followed by rapid drop-casting of 200 \\u03bcL diethyl ether as the anti-solvent within 10 seconds. The pristine MAPbI3 film was accordingly formed by annealing at 100 \\u00b0C for 10 min. For the modified MAPbI3 film preparation, 80 \\u03bcL isopropanol solution of 4-DMABA with a concentration of 2 mg mL\\u22121 was spin-coated onto the pristine MAPbI3 film at a rotation speed of 3000 rpm for 30 s, and was then annealed at 70 \\u00b0C for 10 min. After the perovskite films were prepared, a chlorobenzene solution of PCBM (20 mg mL\\u22121) was spin-coated on top of them at a rotation speed of 1500 rpm for 30 seconds. Subsequently, the saturated methanol solution of BCP was spin-coated on top of the PCBM layer at 6000 rpm for 30 s. Finally, one batch of the films was transferred to the evaporator chamber, and 100 nm thick Ag electrodes were deposited under high vacuum (<3 \\u00d7 10\\u22124 Pa).\\n\\nSEM images were obtained using a Nova Nano 450 scanning electron microscope (FEI Co., Netherlands). XRD characterization was performed on an Empyrean X-ray diffractometer with Cu K\\u03b1 radiation (PANalytical B.V. Co., Netherlands). The infrared spectra were obtained on a VERTEX 70 Infrared Fourier transform microscope (Bruker Co., Germany). The PL spectra were recorded on an Edinburgh FLS920 fluorescence spectrometer (Edinburgh Co., UK). The local photocurrent measurement (pcAFM) was performed using a commercial AFM system (Asylum Research MFP-3D Bio) with Nanosensors PPP-EFM conductive probes, the spring constants of which are about 2.8 N m\\u22121. A solar simulator (Oriel, model 9119) with an AM 1.5G filter (Oriel, model 91192) was used to give an irradiance of 100 mW cm\\u22122. The light intensity was precisely calibrated with a standard Si photodiode detector. The active area of the solar cell was determined to be 0.09 cm2 using a black metal mask. IPCE was measured on a Newport IPCE system (Newport, USA). The long-term stability was measured with a CHI1000c multi-channel electrochemistry workstation (Chenhua Co., China).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiMgLiO,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spray-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 325,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 7,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"N,N\\u2032-Diphenyl-N,N\\u2032-di(m-tolyl)benzidine (TPD) was purchased from Heowns Biochemical Technology Co., Ltd, Tianjin, China. PbI2 and PbBr2 was purchased from Tokyo Chemical Industry Co., Ltd, N,N\\u2032-dimethylformide (DMF) from Alfar Aesar, hydroiodic acid (AR, 45 wt% in water) and methylamine (AR, 27% in methanol) from Sinopharm Chemical Reagent Co. Ltd. 2,2\\u2032,7,7\\u2032-Tetrakis (N,N-di-p-methoxy-phenylamine)-9,9\\u2032-spirobifluorene (spiro-OMeTAD) was from Luminescence Technology Corp., Taiwan, China. Tetrahydrofuran was distilled before using, all the other agents were directly used without further purification. The substrates were FTO conducting glass (Pilkington, thickness: 2.2 mm, sheet resistance: 14 \\u03a9 per square). The patterned FTO glass was first cleaned with mild detergent, rinsed several times with distilled water and subsequently with ethanol in an ultrasonic bath, and finally dried under an air stream.\\n\\nThe as-synthesized compounds were identified by nuclear magnetic resonance (NMR) spectroscopy and high-resolution mass spectroscopy (HRMS). The NMR was obtained on a Bruker AVANCE III 400 MHz spectrometer, with the chemical shifts reported in ppm using tetramethylsilane (TMS) as an internal standard. HRMS was recorded on a SolariX maldi-FTMS mass spectrometer. Ultraviolet-visible absorption (UV-vis) spectroscopy was obtained using a Thermo Evolution 300 UV-visible spectrometer. Decomposition temperature (Td) and glass transition temperature (Tg) were determined by thermo gravimetric analysis (TGA) and differential scanning calorimetry (DSC) on a TA Q500 for thermo gravimetric analysis and a TA Q20 for thermal analysis under a nitrogen atmosphere. The photoelectron yield spectroscopy (PYS) was carried out on the Sumitomo PYS-202 ionization energy detection system. X-ray diffraction (XRD) was measured with a Rigaku Miniflex 600 X-ray diffractometer. Scanning electron microscopy (SEM) was performed with a Hitachi S-4800.\\nCurrent\\u2013voltage characteristics (J\\u2013V) were measured on a Keithley 2602 SourceMeter under AM 1.5 irradiation (100 mW cm\\u22122) from an Oriel Solar Simulator 91192. A mask with a window of 0.16 cm2 was clipped on the TiO2 side to define the photoactive area of the cells. Incident-photon-to-current conversion efficiency (IPCE) was measured by the direct current (DC) method using a lab-made IPCE setup under 0.3\\u20130.9 mW cm\\u22122 monochromic light illumination without bias illumination. Time resolved PL spectra was recorded on a PL spectrometer, Edinburgh Instruments, FLS 900, excited with a picosecond pulsed diode laser (EPL-445), and measured at 775 nm after excitation at 445 nm. The time-of-flight (TOF) measurement was recorded on a TOF401 measurement system, Sumitomo Heavy Industries Ltd. Samples were prepared through spin-coating with the structure of the ITO/as-synthesized compounds (\\u223c1 \\u03bcm)/Al (100 nm) with a working area of 3 \\u00d7 3 mm2.\\n\\nThe designed synthetic routes for the as-synthesized compounds are depicted in Scheme 1, which were synthesized by the Wittig reaction using formyl replaced TPD (2) and Wittig reagents (3) in three steps from commercially available and relatively inexpensive starting reagents. The structures of the as-synthesized compounds were confirmed via1H NMR and MS, which agreed well with the proposed molecular structure (see ESI,\\u2020 Fig. S1).\\n4,4\\u2032-([1,1\\u2032-Biphenyl]-4,4\\u2032-diylbis((4-formylphenyl)azanediyl))bis(2-methylbenzaldehyde) (2). TPD (5.0 g, 9.7 mmol) and imidazole (5.1 g, 61.5 mmol) were added into a two neck 250 mL round bottom flask, followed by 90 mL of acetonitrile. Trifluoroacetic anhydride (17.3 mL, 123.0 mmol) was dropped under a nitrogen atmosphere (N2). Then the above mixture was refluxed until TPD was consumed completely (monitored by thin-layer chromatography). The reaction solution was poured into 1 L water to precipitate a yellow powder. The filter cake was washed with water until the filtrate became colorless, and compound (1) was obtained: yellow solid (15.0 g, 99.1%): mp 243\\u2013245 \\u00b0C, 1H NMR (400 MHz, CDCl3) \\u03b4 (ppm): 2.63 (s, 6H), 6.89 (s, 4H), 7.04\\u20137.24 (m, 14H), 7.53 (d, J = 8.4 Hz, 4H), 7.38 (d, J = 8.5 Hz, 4H), 6.74 (d, J = 10.1 Hz, 8H), 7.27 (s, 4H); ESI-MS (m/z): [M\\u2212] calcd for C66H40F24N10O8, 1556.3; found 1556.9.\\nThe polyimidazoline product ((1), 10 g, 6.4 mmol) was dissolved in 200 mL THF and then pumped with HCl gas (100 mL, 2.5 mol L\\u22121 \\u2013 prepared by adding 21.0 mL of concentrated HCl to 79.0 mL H2O). The reaction solution was refluxed for 12 h. The reaction solution was cooled to room temperature, then an orange solid was formed. The reaction mixture was filtered and recrystallized from diethyl ether, and compound (2) was obtained (3.8 g, 93.0%): mp 197\\u2013199 \\u00b0C, IR: 2803.99, 2722.76, 1693.86; 1H NMR (400 MHz, CDCl3) \\u03b4 (ppm): 10.15 (s, 2H), 9.91 (s, 2H), 7.80 (d, J = 8.5 Hz, 4H), 7.74 (d, J = 8.4 Hz, 2H), 7.62 (d, J = 8.4 Hz, 4H), 7.32\\u20137.21 (m, 8H), 7.19\\u20137.04 (m, 4H), 2.60 (s, 6H); ESI-MS (m/z): [M + H]+ calcd for C42H32N2O4, 628.2; found, 629.5.\\nWittig regents (3). Wittig reagents (3) were synthesized according to the literature.\\nN,N-Di(phenyl)-N\\u2032,N\\u2032-di(4-(4-N,N-di(4-(4-methoxy-phenyl)amino)phenyl)ethenyl)-1,1\\u2032-biphenyl-4,4\\u2032-diamine (TPD-4MeTPA). 4-[N,N-Di(p-tolyl)amino]benzyl(triphenyl)phosphonium bromide (W1, 2.64 g, 4 mmol) and compound (2) (0.31 g, 0.5 mmol) were added into a 100 mL round-bottom flask under N2. Anhydrous THF (40 mL) was added to the above flask, and cooled down to 0 \\u00b0C. The THF solution of t-BuOK (16 mmol, 0.8 mol L\\u22121) was added dropwise to the above flask, stirred for 30 min at 0 \\u00b0C, followed with stirring at room temperature until compound (2) was consumed completely (monitored by thin-layer chromatography). The reaction was terminated with ice water. The crude product was heated under reflux for 8 h in THF with a catalytic amount of iodine. Then the remaining iodine was removed using sodium hydroxide (NaOH) solution (Wt = 10%, 100 mL) by stirring for 2 h. After that, the product was purified by chromatography on a silica gel column (petroleum ether:ethyl acetate = 50:1 as eluent) to give the title compound as a pure E stereoisomer TPD-4MeTPA (0.59 g, 69%): 1H NMR (400 MHz, CDCl3) \\u03b4 (ppm): 7.67 (dd, J = 11.9, 7.9 Hz, 2H), 7.58\\u20137.42 (m, 6H), 7.40\\u20137.28 (m, 10H), 7.20\\u20136.76 (m, 60H), 2.30 (q, J = 5.0 Hz, 30H). HRMS (m/z): calcd for C124H108N6, 1705.86690; found 1705.86589.\\nTPD-4MeOTPA and TPD-4EtCz were synthesized with W2 (4-[N,N-di(p-methoxyphenyl)amino]benzyl(triphenyl)phosphoniumbromide), W3 (3-[(9-ethyl)-carbazole]methyl(triphenyl)phosphonium bromide) and compound 2 using the same method.\\nTPD-4MeOTPA: (0.63 g, 73%): 1H NMR (400 MHz, CDCl3) \\u03b4 (ppm): 7.53\\u20137.43 (m, 6H), 7.37 (d, J = 8.3 Hz, 4H), 7.31 (t, J = 7.2 Hz, 8H), 7.10 (dd, J = 35.0, 7.7 Hz, 26H), 6.91 (s, 16H), 6.83 (d, J = 8.6 Hz, 18H), 3.79 (s, 24H), 2.33 (d, J = 11.3 Hz, 6H). HRMS (m/z): calcd for C126H108N6O8, 1833.82622; found 1833.82536.\\nTPD-4EtCz: (0.51 g, 65%): 1H NMR (400 MHz, CDCl3) \\u03b4 (ppm): 8.15 (dd, J = 24.0, 17.1 Hz, 6H), 7.73\\u20137.63 (m, 4H), 7.59 (t, J = 9.7 Hz, 2H), 7.56\\u20137.27 (m, 22H), 7.22\\u20136.92 (m, 14H), 4.34 (t, J = 12.2 Hz, 8H), 2.39 (d, J = 25.3 Hz, 6H), 1.50\\u20131.35 (m, 12H). HRMS (m/z): calcd for C102H84N6, 1393.67910; found 1393.67831.\\n\\nQuantum chemical calculation was performed on the Gaussian 03 program with the Beck's three-parameter exchange functional and the Lee\\u2013Yang\\u2013Parr's correlation functional (B3LYP) using 6-31G(d) basis sets.\\n\\nA 30 nm-thickness compact TiO2 layer, 200\\u2013300 nm mesoporous TiO2 layers and a perovskite layer ([(FAI)0.85(PbI2)0.85(MABr)0.15(PbBr2)0.15]) were prepared according to the reported methods. The HTM layers were spin-coated on top of the TiO2/perovskite films at 3000 rpm for 20 s with a concentration of 20 mg mL\\u22121. For comparison, perovskite solar cells based on spiro-OMeTAD were also fabricated by using a chlorobenzene solution doped with lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) and 4-tert-butylpyridine (tBP) under the same conditions. All the above fabrication processes were carried out in air. Finally, an 80 nm-thickness Au photocathode was deposited by thermal evaporation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: TPD-4MeTPA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 600,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 94,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The perovskite thin films were deposited using a similar one-step process described in our earlier work. Lead iodide (PbI2, Alfa Aesar, 99.9985%), methylammonium iodide (MAI, Dyesol), formamidinium iodide (FAI, Dyesol), lead thiocyanate (Pb(SCN)2, Sigma-Aldrich, 99.5%), dimethyl sulfoxide (DMSO, Sigma-Aldrich, 99.8%) and N,N-dimethylformamide (DMF, Sigma-Aldrich, 99.8%) were purchased and used without further purification. The perovskite precursor was prepared using a Lewis acid\\u2013base adduct approach with the mixture of MAI, FAI, PbI2, DMSO, and Pb(SCN)2 in DMF, where the molar ratio of DMSO and PbI2 is 1:1. A 45% by weight precursor solution of MAPbI3 was prepared with PbI2, MAI and DMSO (molar ratio = 1:1:1) in DMF. A 3% Pb(SCN)2 with respect to the weight of PbI2 is also added in the solution, which was then stirred for 12 hours on a 60 \\u00b0C hot plate before deposition. The FAPbI3 precursor solution was made in the same process. The MA0.7FA0.3PbI3 precursor was prepared by mixing the two different solutions with the molar ratio of MAI and FAI to be 7:3. The as-resulted precursor solution was stirred for one hour on a 60 \\u00b0C hotplate and then purified using a 0.45 \\u03bcm filter before use. The perovskite precursor solutions were spin-coated on the substrates at 4000 rpm for 60 s with 750 \\u03bcL diethyl ether (Alfa Aesar, 99%) dripped simultaneously during the spinning. The as-deposited film was annealed at 65 \\u00b0C for 2 min and then 100 \\u00b0C for 10 min. The top-view scanning electron microscopy (SEM) image of a perovskite film is shown in Fig. S1 (ESI\\u2020).\\n\\nThe perovskite solar cells were fabricated with a regular device structure of fluorine-doped tin oxide (FTO)/C60-SAM/MA0.7FA0.3PbI3/Spiro-OMeTAD/Au as shown by the cross-sectional SEM image (Fig. S2, ESI\\u2020). FTO glass (Pilkington, NSG TEC-15) was used as the substrates. C60-SAM is a fullerene self-assembled monolayer and serves as an interface passivation layer. MA is CH3NH3 and FA is HC(NH2)2. Spiro-OMeTAD is 2,20,7,70-tetrakis(N,N-bis(p-methoxy-phenyl)amino)-9,90-spirobifluorene, serving as a hole selective layer (HSL). No electron selective layers (ESLs) were used in this work to intentionally increase the current density\\u2013voltage hysteresis. The C60-SAM was deposited following our previous report. The HSLs were prepared by spin coating a Spiro-OMeTAD solution at 2500 rpm for 60 s. The HSL solution was prepared by dissolving 68 mmol spiro-OMeTAD (Shenzhen Feiming Science and Technology Co., Ltd, 99.0%), 26 mmol Li-bis-(trifluoromethanesulfonyl) imide (LiTFSI) (Sigma, 99.95%), and 55 mmol 4-tert-butylpyridine (TBP) (Sigma, 96%) in 1 ml mixed solvent of chlorobenzene and acetonitrile (Sigma, 99.8%) with a volume ratio of 10:1. Finally 80 nm Au was thermally evaporated through a metal mask on the HSLs. The active area of the finished devices was 0.08 cm2.\\n\\nThe SEM images were taken with a Hitachi S-4800 High Resolution microscope. The J\\u2013V curves were measured using a Keithley2400 sourcemeter at different scan rates, with the samples under AM 1.5G (100 mW cm\\u22122) illumination (PV Measurements Inc.). All device characterizations were performed in the ambient air (25 \\u00b0C, 50% humidity).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: C60-SAM,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.7MA0.3PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: SCN,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"In(OH)3 was used as the In source and was dissolved in carbon disulphide (CS2) and n-butylamine mixed solution, forming an In-complex precursor solution. In this system, the reaction between CS2 and n-butylamine generated butyldithiocarbamic acid (BDCA) (Fig. 1). This kind of thiol-amine acid is highly active and thus, it can react with a series of metal oxides and metal hydroxides to form an organometallic complex. First, 1 mmol In(OH)3 (99.99%, Aladdin reagent) powder was dispersed in 1 mL ethanol with magnetic stirring at room temperature. Then, 0.3 mL n-butylamine (99.5%, Aladdin reagent) was added to it. Later, 225 \\u03bcL carbon disulphide (CS2) (99.9%, Aladdin reagent) was introduced into the mixed solution in a dropwise manner. The solution was further stirred for another 2 h to obtain a clear solution (Fig. 1). Here, In-complex formed is indium butyldithiocarbamates (In(S2CNHC4H9)3). The above solution was then filtered with 0.22 \\u03bcm filtrator, and 1 mL filtered solution was diluted with 0.5 mL, 2 mL, 3.5 mL and 5.75 mL ethanol to form 220 mmol L\\u22121, 110 mmol L\\u22121, 75 mmol L\\u22121 and 50 mmol L\\u22121 In-complex precursors, respectively. For In2S3 thin films, different concentrations of In-complex precursor were spin-coated at a speed of 5000 rpm for 40 s on cleaned fluorine-doped tin oxide (FTO). The FTO/glass substrates were treated by UV-ozone treatment for 15 min before deposition of the In2S3 films. This was followed by annealing on a hot plate in an N2-purged glove box at 200 \\u00b0C for only 1 min and at 300 \\u00b0C for 2 min.\\nTiO2 layers were grown by chemical bath deposition on cleaned FTO substrates. The deposition was made by putting the FTO/glass substrates in a glass container filled with titanium chloride solution in a 70 \\u00b0C lab oven for 1 h. The deposited substrates were rinsed with deionized water for 2 min to remove any loosely bound materials, dried in a stream of N2, and annealed for 30 min at 200 \\u00b0C on a hot plate.\\n\\nThe PSC adopted the structure of FTO/TiO2 or In2S3/CH3NH3PbI3/Spiro-OMeTAD/Au. All TiO2/FTO/glass substrates were treated by UV-ozone treatment for 15 min before deposition of the perovskite films. PbI2 was purchased from Alfar Aesar (99.99%), and CH3NH3I was purchased from Xi'an Polymer Light Technology Corp (99.5%). First, 1.1064 g PbI2 and 0.3816 g CH3NH3I were disolved in 1.4 mL \\u03b3-butyrolactone (GBL, 99.9%, Aldrich) and 0.6 mL dimethyl sulfoxide (DMSO, 99.9%, Aldrich) in a glovebox with constant stirring at room temperature to form the perovskite solution. Then, the perovskite solution was spin-coated on top of the ETLs (TiO2 or In2S3) at 1000 rpm for 10 s and at 4000 rpm for 40 s while dripping chlorobenzene (as the antisolvent) onto the substrate during the second spinning step. All the samples were then heated at 100 \\u00b0C for 10 min, resulting in the formation of dark perovskite films. Also, 900 mg Spiro-OMeTAD (90 mg was dissolved in 1 mL chlorobenzene doped with 36 \\u03bcL 4-tert-butylpyridine (TBP, Sigma-Aldrich) and 22 \\u03bcL (520 mg mL\\u22121) lithium bis imide acetonitrile solution) was deposited by spin-coating (5000 rpm for 30 s) as the hole transport layer on top of pervoskite film. Finally, a 100 nm-thick gold electrode was deposited by thermal evaporation using a shadow mask to form an active area of 9 mm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: In2S3,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Unknown,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned ITO glasses with a sheet resistance of 7 \\u03a9 sq\\u22121 and a thickness of 1.1 mm were purchased from Hua Yu United Technology Co. Ltd. Lead iodide (PbI2) and methylammonium iodide (MAI) were purchased from Sigma-Aldrich and Shanghai MaterWin New Materials Co. Ltd, respectively. PEDOT:PSS, rub, and PC61BM were purchased from Heraeus Materials Technology Co. Ltd., Banhe Technology Co. Ltd., and Nano-C, respectively. All solvents used were obtained from Sigma-Aldrich. All materials and solvents were directly used without further purification.\\n\\nITO glasses were washed with acetone, ethanol, and deionized water in sequence, followed by ultrasonic cleaning with deionized water, acetone, and ethanol for 15 min. After drying with high purity N2 and vacuum drying in an oven, the ITO substrates were treated with O3 for 15 min in an UV-ozone cleaner. Then, rub (or PEDOT:PSS) was spin-coated onto the patterned ITO glass substrates at 3000 rpm for 30 s (2000 rpm for 60 s for PEDOT:PSS), forming a 47 nm (50 nm for PEDOT:PSS) thick film, and then dried at 110 \\u00b0C for 20 min (120 \\u00b0C for 30 min for PEDOT:PSS). Similar to a single HTL, the bi-HTL of PEDOT:PSS/rub was treated via a two-step spin-coating process. Note that rub was dissolved in chlorobenzene at a concentration of 30 mg mL\\u22121. To date, these HTL-coated glasses were moved into a glovebox to form a \\u223c300 nm MAPbI3 film via a one-step deposition method. The MAPbI3 solution was prepared by dissolving PbI2 and MAI (molar ratio of 1:1, 40 wt%) into 1 mL of mixed solvent composed of dimethyl sulfoxide (DMSO) and gamma-butyrolactone (GBL) with a volume ratio of 3:7 and then stirring at 70 \\u00b0C for 1 h. The perovskite precursor solution (60 \\u03bcL) was spin-coated on the HTL at 2500 rpm for 90 s, and then, 300 \\u03bcL of chlorobenzene was quickly dropped on the perovskite film. The as-prepared films were then annealed at 100 \\u00b0C for 30 min on a hot plate. During the annealing process, the samples obviously changed from pale yellow to dark brown. After this, 20 mg mL\\u22121 PC61BM in chlorobenzene was spin-coated onto the perovskite layer at 3000 rpm for 60 s in a N2 glovebox. Finally, all the samples were transferred to a vacuum chamber for 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and silver electrode evaporation. Herein, a 6 nm thick BCP and a 100 nm thick Ag were sequentially deposited onto the perovskite layer under a pressure of 6.0 \\u00d7 10\\u22125 Pa through a shadow mask with a defined device area of \\u223c0.1 cm2.\\n\\nThe morphology of the perovskite layer was obtained using a Hitachi S-4800 field emission scanning electron microscope (SEM) and a Bruker atomic force microscope (AFM). The crystal structures of the MAPbI3 thin films were characterized using the Bruker D8 ADVANCE X-ray diffraction (XRD) equipment. The thicknesses of the PEDOT:PSS, rub, perovskite, and PC61BM films were determined using a Bruker DektakXT Stylus Profiler. The current density\\u2013voltage (J\\u2013V) characterization of the perovskite solar cells was carried out using a Keithley 2400 source meter under a simulated AM 1.5 illumination (100 mW cm\\u22122, Oriel Sol3A 94023A Class Solar Simulator) at a scan rate of 200 mV s\\u22121. The UV-vis absorption spectra of the perovskite films and the transmissivity of different HTLs were obtained using a PerkinElmer Lambda 650S spectrophotometer with an excitation wavelength of 400 nm. The photoluminescence measurements were carried out using a Horiba Fluoromax 4 spectrometer. The impedance characteristics of the devices were measured via a Wayne kerr 6500B analyzer. The surface potential of the HTLs (PEDOT:PSS or rub) was measured using a Cypher S atomic force microscope.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 24,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 73.1,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylamine iodide (MAI) and lead(II) iodide (PbI2) were purchased from Sigma-Aldrich. [6,6]-Phenyl-C61-butyric acid methyl ester (PC61BM) was purchased from Lumitech. All chemicals were used as received without further purification. ITO-coated glass was sequentially cleaned with DI water, acetone and isopropyl alcohol, followed by an oxygen plasma treatment for 5 min. For the NiOx layer, nickel acetate precursors (nickel acetate tetrahydrate in monoethanolamine and methoxyethanol solution with a weight percentage of 3%) were spin-coated on the ITO substrates at 3000 rpm for 30 s, and then annealed on a hot plate at 150 \\u00b0C for 10 min, and 350 \\u00b0C for 20 min in air, followed by oxygen plasma treatment for 4 min before further use. After depositing the hole transport layer, the MAPbI3 absorber layer was then deposited by a consecutive two-step spin-coating method; first, a mixture of 1.3 M PbI2 and 0.3 M MAI in anhydrous dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) (9:1, v/v) was spin-coated onto the ITO/NiOx substrates at 6000 rpm for 15 s, and then the speed was decreased to 3700 rpm, and the MAI solution (35 mg mL\\u22121 in isopropanol) was dripped on the spinning substrates after the start of 3700 rpm. Then, the films were dried on a hot plate at 100 \\u00b0C for 30 min. Afterward, the PC61BM solution (20 mg mL\\u22121 in chlorobenzene) with different doping ratios of 2,6-Py was then deposited on top of the formed perovskite layers. For 2,6-Py surface treatment, the 2,6-Py diluted solution in chlorobenzene (1:100, v/v) was directly spin-coated onto the perovskite crystals at 2000 rpm for 60 s. Subsequently, a thin layer (5 nm) of PEI in isopropanol (0.1 wt%) was spin-coated onto the PC61BM layer as a buffer layer to enhance the electron extraction. Finally, 80 nm-thick Ag electrodes were thermally evaporated on top of the devices through a metal shadow mask under high vacuum (<10\\u22127 Torr). The active area of the devices was 0.1058 cm2.\\n\\nLiquid state 1H NMR spectra of the perovskite samples were measured on a Bruker AV400-400 MHz spectrometer in C3D7NO. The absorption spectra of the doped PC61BM films were taken by using a UV-vis-NIR spectrophotometer (UV-3600, Shimadzu). X-ray diffraction (XRD) data of the perovskite films were determined using a Philips diffractometer (X'pert PRO MRD) using Cu K\\u03b1 radiation (\\u03bb = 1.540598 \\u00c5) as the X-ray source at room temperature. The steady-state photoluminescence (PL) spectra were measured at room temperature by using a LabRAM HR800 Roman Microscope with a 150 W Xe lamp as an excitation source at 450 nm. TRPL decay spectra were measured using a Delta Flex Fluorescence Lifetime System monitored at 770 nm. AFM morphology of the films was measured through tapping mode on a Shimadzu SPM9700 under ambient conditions. The electron mobility of the doped PC61BM films was tested in the electron-only device of ITO/ZnO (20 nm)/PC61BM or doped PC61BM/Ca (20 nm)/Al (80 nm) by recording dark current\\u2013voltage through applying sufficient voltage to form the space charge limited (SCLC) current. The SCLC is described by the equation of J = 9\\u03b5r\\u03b50\\u03bcV2/8L3, where \\u03b5r is the dielectric constant of PC61BM (typical value of 3), \\u03b50 is the permittivity of free charge, \\u03bc is the carrier mobility, V is the voltage drop across the device (V = Vappl \\u2212 Vrs \\u2212 Vbi, where Vappl is the applied voltage, Vrs is from contact and series resistance, and Vbi is from built-in voltage), and L is the thickness of the film. The conductivities (in parallel with the substrate) of the doped PC61BM films were calculated according our previous reports. In brief, the doped PC61BM solution is spin-coated onto pre-patterned ITO with a channel length (l) of 0.3 mm and width (a) of 15 mm (Fig. S2\\u2020). The resistance between both ITO electrodes approximately corresponds to the resistance of the doped PC61BM in the channel. The conductivity (\\u03c3) is estimated based on the equation of \\u03c3 = l/(R \\u00d7 a \\u00d7 d), where the d is the thickness of the doped PC61BM films and R represents the resistance obtained from the current\\u2013voltage (J\\u2013V) measurements (Fig. S2\\u2020). The photovoltaic J\\u2013V curves of the as-prepared solar cells were tested in a nitrogen-filled glovebox illuminated under AM 1.5 G irradiation (100 mW cm\\u22122) from a 450 W solar simulator (Newport 94023A-U) and recorded using a Keithley 2400 source-measure unit. The light intensity is calibrated by using a standard silicon solar cell. The scan rate was 20 mV s\\u22121. The external quantum efficiency (EQE) test was performed by using a EQE system equipped with a standard Si diode using a 150 W xenon lamp (Oriel) fitted with a monochromator (Cornerstone 74004) as a monochromatic light source.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PEI,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 200,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.1058,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Zinc acetate dehydrate, tetramethylammonium hydroxide (TMAH), lead iodide, DMSO, DMF, chlorobenzene and toluene were purchased from Sigma-Aldrich and used as received. [6,6]-Phenyl-C61-butyric acid methyl ester (PC61BM) was purchased from American Dyes Source, Inc. CH3NH3I (MAI) was purchased from Shanghai Materwin New Materials Co. Ltd. Poly(bis(4-phenyl)(2,4,6-trimethylphenyl)amine) (PTAA) was purchased from Xi'an Polymer Light Technology Corporation. ZnO nanoparticles were synthesized by a sol\\u2013gel process using Zn acetate dehydrate and TMAH, and dispersed in anhydrous isopropanol with a concentration of 20 mg mL\\u22121.\\n\\nPrior to fabrication, the substrates were cleaned by sonication using detergent, deionized water, acetone, and isopropanol sequentially for every 15 min followed by 15 min of ultraviolet ozone (UV-ozone) treatment. The substrates were transferred to a glovebox. PTAA film was fabricated by spin-coating a toluene solution with a concentration of 5 mg mL\\u22121 on the ITO substrates in glove-box.\\nPbI2 (1 M) and DMSO (1 M) were dissolved in DMF under stirring at 70 \\u00b0C. The solution was then spin coated on the PTAA film at 3000 rpm for 60 s. Then a solution of MAI in 2-propanol (IPA) (50 mg mL\\u22121) was dropped and spin-coated at 3000 rpm for 60 s. Afterwards, the as prepared films were heated at 90 \\u00b0C for 15 min. After cooling down, a layer of PC61BM (20 mg mL\\u22121 in chlorobenzene) was spin-coated at 2000 rpm for 45 s for MAPbI3/PCBM junction solar cells. While for MAPbI3/ZnO junction solar cells ZnO nanoparticles in isopropanol was spin-coated at 4000 rpm for 30 s. Subsequently, samples were loaded into a vacuum deposition chamber (background pressure \\u2248 5 \\u00d7 10\\u22124 Pa) to deposit a 100 nm thick Al cathode with a shadow mask. To specify the illuminated area, we used an aperture with an area of 0.06 cm2, whereas the total device area defined by the overlap of the electrodes was approximately 0.12 cm2.\\nThe J\\u2013V characteristics were measured with Keithley 2400 measurement source units with the devices maintained at room temperature in glove-box. The photovoltaic response was measured under a calibrated solar simulator (Enli Technology) at 100 mW cm\\u22122, and the light intensity was calibrated with a standard photovoltaic reference cell. The devices were stored in glove-box in dark overnight before measurement. The forward J\\u2013V scans were measured from \\u22120.1 V to 1.2 V with a scan rate of 0.05 V s\\u22121 and a voltage step of 0.01 V while the reverse J\\u2013V scans were measured from 1.2 V to \\u22120.1 V with a scan rate of 0.05 V s\\u22121 and a voltage step of 0.01 V. The EQE spectrum was measured using a QE-R Model of Enli Technology.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 90.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 15.0,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 240,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: TRUE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Flexible ITO films were deposited on the PET substrates using an in-line type vertical plasma arc ion plating system at room temperature. The vertical ion plating system (5 generation) consisted of the tray loader, load lock chamber, process chamber, and return chamber. Two sets of electron guns were vertically oriented inside the process chamber (Fig. S1\\u2020). Unlike a typical plasma arc ion plating system, where the plasma beam irradiated on the tablet is located at the bottom of a vacuum chamber, the plasma beam in the in-line arc plasma ion plating system is irradiated from the side to the vertically located ITO tablet (10 wt% Sn-doped In2O3), which directly faces the PET substrate as shown in Fig. 1(a). Using an ITO tablet revolver system (Fig. S1(d)\\u2020), the ITO tablet was supplied in the process chamber without breaking vacuum for continuous coating. The much higher electron density of the arc-discharge plasma compared to the electron density in the sputtering process led to the formation of a high-density plasma beam for sublimation of the ITO tablet. The 10 wt% Sn-doped In2O3 tablet was used to deposit ITO films under a base pressure of less than 1 \\u00d7 10\\u22127 Torr. We employed same composition ITO tablet with typical ITO target used in sputtering process. The PET substrate attached on the in-line tray was supplied to the process chamber through the load-lock chamber. Then, flexible ITO films were deposited on the PET substrates at a constant direct current (DC) power of 3 kW, an Ar/O2 flow rate of 300/90 sccm and a working pressure of 3 mTorr, in increasing processing cycles to handle the thickness of the ITO films. In the vertical ion plating system, the PET substrates could be moved repeatedly between the process chamber and return chamber to control the films thickness.\\n\\nThe electrical and optical properties of the ion-plated ITO films were investigated using the Hall effect measurement (HL5500PC, Accent Optical Technology, HL5500PC) and a UV/Visible spectrometer (UV 540, Unicam) as a function of ITO film thickness. The surface morphology and structure of ion-plated ITO and sputtered ITO films were compared using field emission scanning electron microscopy (FESEM, Carl Zeiss, MERLIN), high resolution transmission electron microscopy (HRTEM, JEOL, JEM-2100F) and atomic force microscope (AFM, SII, SPA-300HV). In addition, the work function of the ion-plated ITO and sputtered ITO films were compared using ultraviolet photoelectron spectroscopy (UPS, Thermo, ESCALAB250). The mechanical flexibility of ion-plated and sputtered ITO films was examined using a lab-made inner and outer bending test system as a function of the radius and bending cycles. The change in resistance of the ion-plated and sputtered ITO films can be expressed as \\u0394R = (R \\u2212 R0)/R0, where R0 is the initial measured resistance, and R is the resistance measured under ITO bending.\\n\\nTo fabricate the flexible ITO-based planar type MAPbI3 perovskite hybrid solar cells, we cleaned the flexible ITO substrate by ultrasonication in 5% Helmanex soap in de-ionized water, ethanol and then isopropyl alcohol. After solvent cleaning, we conducted an Ar plasma treatment on the flexible ITO substrate to remove the organic residues. We prepared ZnO nano-sol as a ZnO electron conductor by a reported method. Briefly, 1.64 g zinc acetate dehydrate (Aldrich) and 0.5 g ethanolamine (Aldrich) were dissolved with vigorous stirring in 10 g 2-methoxyethanol (Aldrich) at 60 \\u00b0C for 30 min. To form the ZnO electron conducting layer on the flexible ITO substrate, we fixed the PET/ITO substrate on a glass substrate with double-sided adhesive film for spin-coating process of ZnO nano-sol and spin-coated the ZnO nano-sol solution at 2000 rpm for 60 seconds and then dried it at 150 \\u00b0C for 10 min. We prepared the 40 wt% of MAPbI3 perovskite solution by mixing MAI (DSLogics. Co., Ltd) and PbI2 (Aldrich) (1:1 mole ratio) in N,N-dimethylformamide (DMF, Aldrich) at 60 \\u00b0C for 30 min. We then added hydriodic acid to the MAPbI3 perovskite solution. To prepare the MAPbI3 thin film on the ZnO/flexible ITO substrate, we spin-coated the 40 wt% of MAPbI3 perovskite solution with hydriodic acid (40 wt% MAPbI3 in DMF solution/hydriodic acid = 1 mL/100 \\u03bcL) at 3000 rpm for 200 seconds and dried it on a hot plate at 100 \\u00b0C for 2 min. Afterwards, we deposited the poly-triarylamine (PTAA, EM index) hole conductor with additives on the MAPbI3/ZnO/flexible ITO substrate by spin-coating PTAA/toluene (15 mg/1 mL) with 7.5 \\u03bcL Li-bis(trifluoromethanesulfonyl)imide (Li-TFSI, Aldrich)/acetonitrile (170 mg/1 mL) and 7.5 \\u03bcL tert-butylpyridine (t-BP, Aldrich)/acetonitrile (1 mL/1 mL) additives at 3000 rpm for 30 seconds. Finally, we deposited an Au counter electrode by thermal evaporation. The active area was fixed at 0.16 cm2. All device fabrications were conducted below 25% relative humidity.\\n\\nThe current density\\u2013voltage (J\\u2013V) curves were measured using a solar simulator (Peccell, PEC-L01) with a potentiostat (IVIUM, IviumStat) under illumination of 1 sun (100 mW cm\\u22122 AM 1.5G), which was calibrated using a Si-reference cell certificated by JIS (Japanese Industrial Standards). The J\\u2013V curves of all devices were measured by masking the active area with a metal mask of 0.096 cm2. The forward and reverse scan speed of J\\u2013V measurement was fixed to 10 mV per 200 ms (50 mV s\\u22121). The external quantum efficiency (EQE) was measured using a power source (ABET 150 W Xenon lamp, 13014) with a monochromator (DONGWOO OPTORN Co., Ltd, MonoRa-500i) and a potentiostat (IVIUM, IviumStat).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: PET | ITO,\\n ETL_stack_sequence: ZnO-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: HI,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.096,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite solar devices were fabricated on FTO-coated glass (Pilkington-TEC15) patterned by laser etching. Before the deposition, the substrates were cleaned using Hellmanex\\u00ae solution and rinsed with deionized water and ethanol. Thereupon, they were ultrasonicated in 2-propanol and dried by using compressed air. The TiO2 blocking layer was deposited onto the substrates by spray pyrolysis at 450 \\u00b0C, using a titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol, Sigma Aldrich) diluted in ethanol (1:14, v/v), with oxygen as the carrier gas. The TiO2 compact layer was then kept at 450 \\u00b0C for 30 min for the formation of the anatase phase. Once the samples achieve room temperature, a TiO2 mesoporous layer was deposited by spin coating at 2000 rpm for 10 s using a commercial TiO2 paste (Dyesol, 18NR-T) diluted in ethanol (1:5, weight ratio). After drying at 100 \\u00b0C for 10 min, the TiO2 mesoporous layer was heated at 500 \\u00b0C for 30 min and later cooled to room temperature. An additional doping treatment using Li+ ions (10.04 mg LiTFSI in 1 mL acetonitrile, 35 mM) was used for the TiO2 mesoporous layer prior to CsPbBr3 deposition.\\nFor MAPbI3 based devices, a pure methylammonium lead iodide solution was prepared to be deposited by spin coating using a methodology previously reported: the perovskite precursor solution was adjusted to the relative humidity of the environment (42% R.H.) by the Pb/DMSO ratio. The perovskite precursor solution (50 \\u03bcL) was spin-coated in a one-step setup at 4000 rpm for 50 s. During this step, DMF is selectively washed with non-polar diethyl ether just before the white solid begins to crystallize in the substrate. For CsPbBr3 based devices a two-step sequential deposition technique was employed. Firstly, a dissolution of PbBr2 in DMF (1 M) was prepared by heating at 75 \\u00b0C for 20 min and filtered (pore size 0.45 \\u03bcm). This solution was spin-coated (2500 rpm \\u2013 30 s) on a TiO2 mesoporous film. During the deposition process, the dissolution was kept at 75 \\u00b0C. Afterward, the substrate was dried on a hot plate at 70 \\u00b0C for 30 min. Subsequently, the substrates were dipped for 10 min in a solution of 17 mg mL\\u22121 CsBr in methanol at 60 \\u00b0C. Then, the substrates were annealed at 250 \\u00b0C for 10 min.\\nFor both the MAPbI3 and CsPbBr3 based devices, Spiro-OMeTAD was deposited as a hole selective material by dissolving 72.3 mg in 1 mL of chlorobenzene as well as 17.5 \\u03bcL of a lithium bis(trifluoromethylsulphonyl)imide (LiTFSI) stock solution (520 mg of LiTFSI in 1 mL of acetonitrile), and 28.8 \\u03bcL of 4-tert-butylpyridine (TBP). The Spiro-OMeTAD was spin coated at 4000 rpm for 30 s. The solution was filtered with a 0.2 \\u03bcm PTFE filter prior to its deposition. Finally, 60 nm of gold was deposited as a metallic contact by thermal evaporation under a vacuum level between 1 \\u00d7 10\\u22126 and 1 \\u00d7 10\\u22125 torr. All the deposition processes were carried out outside a glovebox under environmental conditions.\\n\\nCurrent\\u2013voltage characteristics of the devices were obtained using a solar simulator (ABET-Sun2000) under 100 mW cm\\u22122 illumination with an AM 1.5G filter. The light intensity was recorded using a reference mono-crystalline silicon solar cell with temperature output (ORIEL, 91150). A metal mask was used to define an active area of 0.16 cm2. The current\\u2013voltage characteristics were determined by applying an external potential bias to the cell and measuring the photocurrent using an Autolab/PGSTAT302N potentiostat. The current\\u2013voltage characteristics were measured with a scan rate of 100 mV s\\u22121 and a sweep delay of 20 s. Incident Photon-to-current Conversion Efficiency (IPCE or EQE) was measured using an Oriel Xenon lamp coupled to a McPherson monochromator. Light intensity was determined as a function of the wavelength using a calibrated silicon photodiode (PH-100 Si, GENTECE).\\nThe illumination for the IS measurements was provided by a white LED over a wide range of DC light intensities. Two types of IS experiments were performed: (1) at open circuit (OC) under varying illumination intensities (parameters are extracted, analyzed and plotted as a function of the resulting open-circuit photopotential) and (2) under non open circuit (NOC) conditions with varying DC potential (voltage) while light intensity is fixed. In this latter case the parameters are corrected for voltage drop due to the resulting DC current and the corresponding series resistance. In this work, we will use the labels OC and NOC to refer to these two kinds of experiments. Under both OC and NOC conditions a 20 mV perturbation in the 106 to 10\\u22122 Hz range was applied. A response analyzer module (PGSTAT302N/FRA2, Autolab) was utilized to analyze the frequency response of the devices.\\nIMPS measurements were carried out by coupling the PGSTAT302N/FRA2 module to the LED. IMPS measurements were performed at short-circuit with a light perturbation corresponding to 10% of the DC background illumination intensity. Due to limitations of the experimental set-up, the measurement was limited to the 105 to 10\\u22121Hz frequency range. The NOVA 1.7 software was used to generate data. Z-view equivalent circuit modelling software (Scribner) was used to fit the spectra.\\nFor the structural characterization, Scanning Electron Microscope (SEM) images of the samples were obtained using a Zeiss GeminiSEM-300 microscope working at 2 keV. Energy Dispersive Spectroscopy (EDS) was performed using a Silicon Drift Detector (Oxford Instruments). For optical characterization, UV-visible absorption spectra were recorded by using a Cary 100 UV-Vis spectrophotometer (Agilent) in the range of 400\\u2013800 nm. Steady state photoluminescence measurements were performed using a Hitachi, F-7000 Fluorescence spectrophotometer. Temperature-dependent experiments were carried out by means of a MHCS622CD Heating and Cooling Vacuum/gas tight Stage configured with a MTDC600 temperature controller (Microptik).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The CH3NH3PbI3 layers were prepared in a N2-purged glove box using a CH3NH3PbI3 precursor solution containing 40 wt% of synthesized CH3NH3I powder and PbI2 in \\u03b3-butyrolactone:dimethyl sulfoxide (7:3). This solution was spin-coated onto the compact TiO2 layers by two consecutive spin-coating steps at 1000 and 5000 rpm for 90 and 30 s, respectively. During the second spin-coating step, toluene (1 mL) was introduced dropwise onto the substrate. The substrate was then dried on a hot plate at 100 \\u00b0C for 10 min. To investigate the influence of modifying the CH3NH3PbI3 interface with ALD\\u2013Al2O3, ultrathin Al2O3 films were deposited either beneath or above the spiro-OMeTAD layer on CH3NH3PbI3. Because of the humidity sensitivity of CH3NH3PbI3, trimethylaluminum (TMA, Al3(CH3)3) and ozone were chosen as the aluminum and oxygen sources, respectively, to deposit Al2O3 layers using the ALD method. High purity nitrogen gas was used as both the carrier and purge gases. In each ALD cycle, TMA was dosed into the reactor for 100 ms, which was then purged for 2 s before and after O3 was dosed into the reactor for 200 ms. In this study, the deposition temperature was 70 \\u00b0C, which is lower than the commonly used temperature of 200 \\u00b0C. This lower temperature was chosen because of the relatively low thermal stability of CH3NH3PbI3 and spiro-OMeTAD and the strong oxidation characteristics of O3. The deposition rate was 0.1 nm per cycle. The crystal structures of the films were determined by X-ray diffraction (XRD) analysis with Cu K\\u03b1 radiation (D/max 2500 PC, Rigaku Corporation, Japan; 2theta/theta, \\u03bb = 0.1542 nm) at 40 kV.\\n\\nUsually, devices are constructed from the bottom (the side from which the light is incident) on fluorine-doped tin oxide (FTO)-coated glass that is coated with a compact layer of n-type TiO2, which acts as the electron selective contact. The perovskite layer is then deposited on the n-type compact layer, followed by the p-type hole-conductor, which ensures the collection of holes selectively at the silver cathode. To investigate the influence of the ALD\\u2013Al2O3 interface modification on the performance of the organic\\u2013inorganic hybrid solar cells, three different solar cells were fabricated: FTO/TiO2/CH3NH3PbI3/spiro-OMeTAD/Ag, FTO/TiO2/CH3NH3PbI3/Al2O3/spiro-OMeTAD/Ag, and FTO/TiO2/CH3NH3PbI3/spiro-OMeTAD/Al2O3/Ag. The 30 nm thick TiO2 layers were deposited using a sol\\u2013gel method with titanium isopropoxide. The back contact, consisting of a 120 nm thick silver layer, was thermally evaporated.\\nThe photovoltaic characteristics were measured under 100 mW cm\\u22122 (AM 1.5) illumination using a Keithley 2400 source meter. A solar simulator (500 W Xe lamp) (Japan SAN-EI ELECTRIC XES-40S1) was employed as the light source and the incident light intensity was calibrated by simultaneously using a standard silicon solar cell and a light intensity meter (Radiometer FZ-A). All measurements were performed in air at room temperature with a humidity of 45\\u201350%. Electrochemical impedance spectra (EIS) were conducted using a Zahner IM6ex electrochemical workstation in the dark with a bias of 0.9 V. A perturbation of 10 mV was applied, and the frequency ranged from 1 MHz to 1 Hz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD | Al2O3,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | ALD,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 576,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Stock solutions of CH3NH3PbI3 and CH3NH3PbBr3 were prepared by dissolving stoichiometric ratios of PbX2 and CH3NH3X (X = I, Br) in a DMSO and GBL solution (7:3) at 1.25 M and stirred for 60 min at 50 \\u00b0C and room temperature, respectively. To obtain a range in CH3NH3Pb(I(1\\u2212x)Brx)3, the stock solutions were combined in volumetric ratios. Thin film samples were prepared on glass using the anti-solvent technique adapted from a previously reported method. Glass was washed in soap, acetone, and 2-propanol followed by a 10 min oxygen plasma treatment. The perovskite precursor solution was coated using a spin coating procedure using two speeds where toluene was dripped onto the surface during the second step and then dried at 100 \\u00b0C post deposition. The resulting films had thicknesses of 236 \\u00b1 7 nm, as measured by alpha step 200.\\n\\nStability analysis of thin film materials was done in a glovebox with an LED light, humidity control, and atmospheric control between nitrogen and dry air. The light source was calibrated to current match a CH3NH3PbI3 device under an AM1.5 solar spectrum to obtain a 1 sun equiv. LED intensity. The Bridgelux 4000 K LED spectrum covers the visible spectrum, with negligible UV. Dry air conditions were obtained from bottled gas of a nitrogen and oxygen mix, at 21% oxygen concentration (BOC 12-X). Optical characterisation of samples was monitored with a digital camera, and the change in the average RGB output values was monitored against background values according to eqn (1): where RGBt is the average red-green-blue pixel value at time t, RGBdeg is the fully degraded sample, and RGB0 is the initial value at t = 0.\\n\\nCells were manufactured following a previously reported procedure. In summary, FTO coated glass substrates were coated with compact TiO2 by spray pyrolysis of a 20 mM titanium diisopropoxide bis(acetylacetonate) solution (Aldrich) at 450 \\u00b0C. A mesoporous TiO2 layer was deposited from a commercially available paste (18-nrt, dyesol) diluted 2:13 wt with ethanol before spin coating at 2000 rpm for 30 seconds and sintering at 450 \\u00b0C. Next a perovskite precursor solution was made using the same method as described for the film preparation. The perovskite precursor solution was coated using a spin coating procedure using two speeds where toluene was dripped onto the surface during the second step and then dried at 100 \\u00b0C post deposition. In instances where spiro-OMeTAD was used as a HTM, a solution of 8% wt 2,2\\u2032,7,7\\u2032-tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9\\u2032-spirobifluorene (spiro-OMeTAD, Borun Chemical) in chlorobenzene was next spin-coated onto the perovskite films. The spiro-OMeTAD solution contained additives including 19 mM bis(trifluoromethane)sulfonimide lithium salt (Li-TFSI) and 7 mM 4-tert-butylpyridine (tBP). Oxidising dopant V2O5 (99.99%, Aldrich) was also added to the spiro-OMeTAD solution in the amount of 2.5% wt with respect to the spiro-OMeTAD powder. In instances where P3HT was used as a HTM, a 12 mg mL\\u22121 solution of high molecular weight poly(3-hexylthiophene) (P3HT) (Mw 135k, PDI 1.5, RR 99%) in chlorobenzene was spin-coated onto perovskite films at 2000 rpm for 30 s. Finally, a 50 nm Au contact was evaporated onto the cell under vacuum leaving an active area of 0.15 cm2.\\n\\nInitial current\\u2013voltage characteristics were measured using a xenon lamp under AM1.5 solar illumination (Oriel Instruments) calibrated to a silicon reference cell with a Keithley 2400 source meter. Cyclic scans were performed from 0 V to 1.5 V forward bias and back to 0.5 V reverse bias at a rate of 0.125 V s\\u22121 as shown in Fig. S2.\\u2020 Cells were unmasked during measurements, using the area created by the overlap of the metallic contact and the FTO substrate as the defined active area of 0.15 cm2. During stability measurements, the current\\u2013voltage scan was performed from 1.5 V forward bias to \\u22120.5 V reverse bias and held at open circuit conditions between measurements. Atmospheric conditions of device stability performance were monitored using the environmentally controlled glovebox described in the thin film characterisation.\\n\\nX-ray diffraction (XRD) measurements on thin film samples with glass substrates were performed using a Bruker D8 Discover X-ray diffractometer equipped with Ni-filtered Cu K\\u03b1 radiation (\\u03bb = 1.5406 \\u00c5) operating at 40 kV and 40 mA. XRD patterns were acquired in the Bragg\\u2013Brentano geometry with a standard 2\\u03b8 step size of 0.01671 degree from 10 degree to 40 degree at 26 s per degree.\\n\\nSub-microsecond timescales transient absorption spectroscopy (us-TAS) decays were acquired on a custom-built system. Samples were excited at 420 nm (40 \\u03bcJ cm\\u22122) by using an Opolette 355 laser (OPOTEK), white probe light generated by a tungsten halogen lamp and detected by using a silicon photodiode detector. A probe wavelength of 530 nm was selected by a monochromator and long pass optical filters were used to limit light exposure to the sample and reduce the effect of laser scatter. Samples were measured in an N2 or dry air atmosphere, as required.\\n\\nA stock solution (31.7 \\u03bcm) of the hydroethidine (HE) probe was prepared by dissolving 10 mg HE in 10 mL of dry toluene; sonication was used to facilitate miscibility. Films were then added to 10 mL of 0.317 \\u03bcm solution created from the stock solution. Photoluminescence spectra were recorded using an excitation wavelength of 520 nm and a slit width of 10 nm on a Horiba Jobin-Yvon Fluorolog-3 spectrofluorometer. In the experiments involving oxygen, dry oxygen was bubbled through the toluene. Spectral mismatch correction for the varying ratio of halide is calculated with eqn (2): where IF(t) is the average fluorescence intensity from 605\\u2013615 nm at time t, IF(t0) is at t = 0 min and \\u03b2 is the spectral mismatch factor relative to CH3NH3PbI3 as given in Table S4.\\u2020\\n\\nPotassium superoxide and methylammonium bromide were dissolved in a 1:1 molar ratio in dry ethanol. The reaction was monitored by 1H NMR using a 400 MHz Bruker spectrometer. Deuterated acetone was added to the solution prior to the NMR spectroscopy for calibration of the spectrum.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 35.0; 35.0,\\n Stability_atmosphere: Dry air,\\n Stability_time_total_exposure: 5,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI, CH3NH3I) was synthesized by reacting 27.86 mL of methylamine (40% in methanol, TCI) and 30 mL of hydroiodic acid (57 wt% in water, Aldrich) in a 250 mL round bottom flask at 0 \\u00b0C for 4 h with stirring. The precipitate was obtained by evaporation at 50 \\u00b0C for 40 min. The product CH3NH3I was washed three times with diethyl ether. Finally, the resultant white powder was dried in a vacuum oven for 24 h at 60 \\u00b0C. Lead(II) iodide (PbI2) was purchased from Alfa Aesar. PEDDOT:PSS Clevios PVP AI 4083 was purchased from Heraeus, Germany.\\n\\nPerovskite film fabrication. The perovskite precursor solution for the ternary system was prepared by mixing 1.5 M PbI2 and 1.5 M MAI with 1 mL of solution consisting of GBL:DMSO:NMP with a solvent molar ratio of 2:2:1. For the binary system film, the precursor solution was prepared by mixing PbI2 and MAI with the same molar ratio with 1 mL of solution consisting of GBL and DMSO, with a solvent molar ratio of 1:1. To prepare perovskite films, 200 \\u03bcL of perovskite precursor solution was spin-coated onto the ITO/PEDOT:PSS substrates at 1000 rpm and 7000 rpm for 10 s and 35 s respectively. During the spin-coating, 1 mL of anhydrous chlorobenzene was quickly dropped on the center of the substrates after 20 s. Afterwards, the spin-coated films were annealed on a hot plate for 1 h at 85 \\u00b0C.\\nSolar cell fabrication. The planar perovskite photovoltaics were fabricated with the structure: glass/ITO/PEDOT:PSS/perovskite/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM)/lithium fluoride (LiF)/Al. Indium tin oxide (ITO) substrates were ultrasonically cleaned with isopropyl alcohol, acetone and isopropyl alcohol, respectively. After drying in the oven, the ITO substrates were treated with UV-ozone for 20 min. The PEDDOT:PSS solution was spin-coated onto ITO at 5000 rpm (as a hole transport layer), followed by drying on a hotplate at 150 \\u00b0C for 20 min in air. The substrates were then transferred to an Ar-filled glove box. The precursor solutions were filtered using 0.45 \\u03bcm polyvinylidene fluoride (PVDF) filters and spin-coated onto a PEDOT:PSS layer in two consecutive steps (1000 rpm, 10 s; 7000 rpm 60 s). After the formation of MAPbI3 films, 15 mg mL\\u22121 PCBM dissolved in CB was spin-coated onto the MAPbI3 films at 1000 rpm for 1 min. The device fabrication was completed by the thermal evaporation of 0.5 nm LiF and a 100 nm aluminum electrode. Fifty devices under each conditions were fabricated and tested.\\n\\nThe current\\u2013voltage (I\\u2013V) curves of the devices were recorded using a Keithley 2400 Source Measure Unit. An AM 1.5 G simulator was used (McScience K201 LAB50, Oriel) to simulate the solar spectrum. UV-visible absorption spectra were measured using a UV-2450 (SHIMADZU, Japan). Field emission scanning electron microscopy (FE-SEM) images were obtained using a JSM-6700F (JEOL, Japan). The photoluminescence (PL) spectra of the films were obtained using a LS 55 (Perkin Elmer, USA). AFM images were obtained by using a XE-70 (Park Systems Corp., Korea). The MAPbI3 film properties were characterized by powder X-ray diffraction (XRD) (Rigaku D/Max 2200), using Ni-filtered Cu/K\\u03b11 radiation (\\u03bb = 1.5418 \\u00c5). The external quantum efficiency (EQE) and the internal quantum efficiency (IQE) were measured with monochromatic light generated from a 300 W xenon lamp in the range 300\\u2013900 nm using a K3100 EQX (McScience, Korea). The thermogravimetric analysis was conducted using the TA Instruments Q500. The measurements were conducted from 25 \\u00b0C and continually enhancing the temperature to 800 \\u00b0C at a speed of 10 \\u00b0C min\\u22121 under the N2 atmosphere. Fourier transform infrared spectroscopy (FTIR) was performed using a Scimitar Series FTS800 (Varian, US).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 85,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Ambient,\\n Stability_time_total_exposure: 50,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 30,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped SnO2-coated transparent conducting glass (FTO, 15 \\u03a9 per square) was obtained from Pilkington TEC. CH3NH3I (MAI, 99%) and 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (spiro-OMeTAD) were purchased from Xi\\u2019an Polymer Light Technology Corp. Titanium isopropoxide (98%), lithium bis(trifluoromethylsulphonyl) imide (Li-TFSI, 99.99%) and 4-tert-butylpyridine (TBP, 96%) were bought from Aldrich. Bis(acetylacetonate) (99%), isopropanol (IPA, 99.7%), N,N-dimethylformamide (DMF, 99.9%) and hydrogen chloride isopropanol solution (IPA HCl, for GC, \\u223c1.25 M (T)) were purchased from J&K Chemicals. TiO2 (particle size: about 30 nm, crystalline phase: anatase) was obtained from Dysol. Lead(II) iodide (PbI2, 99.999%) was purchased from TCI. All chemicals were used as received without further purification.\\n\\nA 50 nm-thick TiO2 compact blocking layer (c-TiO2) was deposited on the clean and etched FTO substrate by aerosol spray pyrolysis at 450 \\u00b0C, using a precursor solution of 0.4 mL of bis(acetylacetonate) and 0.6 mL of titanium diisopropoxide in 7 mL of isopropanol. A mesoporous TiO2 layer (100\\u2013150 nm in thickness) was then deposited on the c-TiO2/FTO substrate by spin coating at 5000 rpm for 30 s. After drying at 100 \\u00b0C, the mesoporous TiO2 film was annealed at 510 \\u00b0C for 20 min to remove the organic residue. For depositing the MAPbI3 perovskite layer, first a layer of PbI2 was spin-coated on top of the mesoporous TiO2 layer from a 1.0 M PbI2 DMF precursor solution (with or without an IPA HCl additive) at 2500 rpm for 30 s, then a 45 mg mL\\u22121 MAI IPA solution was spin coated on the PbI2 film at 2500 rpm for 30 s immediately. The deposited film was then annealed at 105 \\u00b0C for 60 min to form the perovskite layer. The HTM layer was deposited onto the perovskite layer by spin-coating at 2500 rpm for 20 s, using a solution of spiro-MeOTAD, 4-tert-butylpyridine, and lithium bis(trifluoromethylsulphonyl) imide and the Co(III)-complex. Finally, a 60\\u201380 nm-thick Au counterelectrode was deposited by thermal evaporation on the top of the device.\\n\\nPhotocurrent and voltage curves (J\\u2013V) were measured with a solar simulator equipped with a 450 W xenon lamp (AAA simulator, Oriel USA) and a Keithley 2400 source meter. The light intensity was adjusted with an NREL-calibrated Si solar cell with a KG-2 filter for approximating 1 sun light intensity (100 mW cm\\u22122). While measuring the current and voltage, the cell was covered with a black mask to define the active area of the device, and in this case it was 0.09 cm2. The incident monochromatic photon-to-current conversion efficiency (IPCE) was measured using an IPCE measuring system (Newport Corporation, CA) equipped with a Xe lamp as the light source. Time-resolved photoluminescence (TR-PL) spectra were collected using a transient state spectrophotometer (F900, Edinburgh Instruments). The samples were excited with a 660 nm pulsed diode laser with a repetition rate of 2.5 MHz and an excitation intensity of about 14 nJ cm\\u22122. Steady-state fluorescence (PL) spectra were recorded by exciting the perovskite films without or with a TiO2 layer at 473 nm with a standard 450 W xenon CW lamp. The signals were recorded using a spectrofluorometer (Photon Technology International) and analyzed using the software Fluorescence. The morphologies of the PbI2 and CH3NH3PbI3 (MAPbI3) films were characterized using a field-emission scanning electron microscope (FE-SEM, ZEISS \\u03a3IGMA) and atomic force microscopy (AFM, using a MultiMode V (Veeco) viewer and analyzer). The X-ray diffraction spectra of the PbI2 and MAPbI3 films were recorded on an X\\u2019pert PRO X-ray diffractometer. The data were collected at room temperature in the 2\\u03b8 range 10\\u201360\\u00b0. Ultraviolet-visible (UV-vis) absorption spectra of all samples were measured using an UV-vis spectrophotometer (U-3900H, HITACHI, Japan) at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: IPA HCl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 105.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 60.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Co; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead(II) iodide (PbI2, 99%), tin(II) iodide (SnI2, 99.99%), lead(II) bromide (PbBr2, 99.999%), cesium iodide (CsI, 99.999%), tin(II) fluoride (SnF2 99%), toluene (anhydrous, 99.8%), chloroform (\\u226599.99%), \\u03b3-butyrolactone (GBL, \\u226599%), N,N-dimethyl sulfoxide (DMSO, anhydrous, \\u226599.9%), and bathocuproine (BCP, 96%) were purchased from Sigma-Aldrich (St. Louis, Missouri) and used without further purification. Methylammonium iodide (MAI), formamidinium iodide (FAI), and formamidinium bromide (FABr) were purchased from Greatcell Solar (Queanbeyan, Australia) without further purification. The PC60BM (>99.5%) and C60 (>99.5%) were purchased from American Dye Source (Quebec, Canada).\\n\\nThe perovskite precursor solutions were prepared by dissolving MAI, FAI, PbI2, PbBr2, SnI2, and FABr at the corresponding molar ratios in GBL and DMSO (volume ratio 7:3) with a total concentration of 2.5 M. A 10% SnF2 per molar weight of SnI2 was added to the precursor solution as a reducing agent. CsI was dissolved in DMSO at a concentration of 1.5 M and added to the precursor to achieve the correct triple cation composition. The precursors were mixed at 60 \\u00b0C for 1 h and were filtered through a 0.2 \\u03bcm PTFE filter before use. Plain glass was cut into 15 mm \\u00d7 15 mm substrates which were then cleaned via ultrasonication for 15 min in detergent in Millipore deionized water, acetone, and isopropanol in sequence. The substrates were treated with oxygen plasma under 100 W for 10 min. A 70 \\u03bcL drop of precursor solution was spin-coated on a cleaned glass substrate at 500 rpm for 5 s, 1000 rpm for 15 s, and 4000 rpm for 40 s in a nitrogen glove box. A toluene anti-solvent was in situ dripped onto the substrate during the last 15 s of the third spin-coating step. The volume of the anti-solvent was decreased from 800 to 700, 600, 500, and 500 \\u03bcL for Csx(MA0.17FA0.83)1\\u2212xPb1\\u2212ySny(I0.83Br0.17)3 perovskites with y = 0, 0.25, 0.5, 0.75 and 1.0, respectively. The perovskite films were then thermally annealed at 100 \\u00b0C for 10 min.\\n\\nScanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) were acquired using a FEI Sirion SEM operated at 5 kV and 15 kV to determine the surface morphology and elemental compositions of perovskite thin films, respectively. Two-dimensional X-ray diffraction (XRD) patterns were collected with a Bruker GADDS D8 Focus Powder Discover diffractometer using Cu K\\u03b1 radiation (\\u03bb = 1.5419 \\u00c5) and the data were processed using the EVA package provided by Bruker Axs to investigate the crystalline structures of perovskite thin films. Ultraviolet-visible (UV-Vis) absorption spectra were collected using a Varian Cary 5000 UV-Vis-NIR spectrophotometer. Photoluminescence (PL) spectra were obtained with a modified Horiba LabRAM HR-800 with 532 nm laser excitation and a Czerny-Turner monochromator blazed at 1200 nm. Measurements were conducted at 1 Sun above the band gap equivalent photon flux with a 532 nm cw laser. The PL experiments were conducted in a N2-filled KF flange with a borosilicate glass window.\\n\\nITO coated glass substrates (10 ohm sq\\u22121 ITO, Colorado Concept Coatings LLC) were cut and cleaned as described above. The PEDOT:PSS (Al 4083, Heraeus Clevios\\u2122) solution was filtered with a 0.45 \\u03bcm nylon filter. A 70 \\u03bcL drop of PEDOT:PSS was spin-coated on a cleaned ITO coated glass substrate at 5000 rpm for 60 s and annealed at 150 \\u00b0C for 10 min in air. The substrates were transferred to a glove box and the perovskite thin films were fabricated as described above. A PC60BM solution (15 mg ml\\u22121 in chloroform) was then spin coated on the perovskite films at 4000 rpm for 60 s and dried without annealing. The substrates were loaded into a thermal evaporation chamber to thermally deposit 20 nm of C60 and 8 nm of BCP. Finally, a mask with 3.14 \\u00d7 10\\u22126 m2 area holes was placed on devices to evaporate 150 nm of silver for electrodes in a high vacuum evaporator (<1 \\u00d7 10\\u22126 torr). The resulting device structure is ITO/PEDOT:PSS/perovskite/PC60BM/C60/BCP/Ag.\\n\\nThe photocurrent density\\u2013voltage (J\\u2013V) curve measurements were conducted in a N2 glovebox with a Keithley 2400 Source Meter and a Solar Light Co. Xenon lamp (16S-300 W) and an AM 1.5 filter. Before measurements, the light intensity was calibrated to 100 mW cm\\u22122 using a standardized National Renewable Energy Laboratory calibrated silicon solar cell. EQE measurements were performed under ambient conditions without encapsulation using a xenon lamp (Oriel, 450 W) light source, a monochromator (Newport Cornerstone 130), an optical chopper, a lock-in amplifier (Stanford Research Corp SR830), and finally a NIST-certified Si-photodiode (Thorlabs FDS 100-CAL) for calibration.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation | Evaporation,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16Pb0.25Sn0.75Br0.5I2.5,\\n Perovskite_composition_short_form: CsFAMAPbSnBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 120,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 55,\\n Cell_area_measured: 0.0314,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A schematic illustration showing the fabrication processes used to fabricate photovoltaic cells is shown in Fig. 1 . All processes were performed in air [26\\u201328]. F-doped tin oxide (FTO) substrates were cleaned in an ultrasonic bath with acetone and ethanol, and dried under nitrogen gas. Subsequently, the FTO substrates were treated with an ultraviolet ozone cleaner (Asumi Giken ASM401N) for 15\\u202fmin. TiOx precursor solutions (0.15 and 0.30\\u202fM) were prepared from titanium diisopropoxide bis(acetyl acetonate) (Sigma Aldrich) and 1-butanol (Wako Pure Chemical Industries). Both TiOx precursor solutions were spin-coated onto the FTO substrate at 3000\\u202frpm for 30\\u202fs (Mikasa MS-A100) and annealed at 125\\u202f\\u00b0C for 5\\u202fmin, however, the 0.30\\u202fM precursor was spin-coated twice to form a uniform layer. After that, the FTO substrate was sintered at 550\\u202f\\u00b0C for 30\\u202fmin to form a compact TiO2 layer. A mesoporous TiO2 layer was spin-coated on top of the compact TiO2 layer at 5000\\u202frpm for 30\\u202fs using TiO2 paste. The TiO2 paste was prepared using TiO2 powder (Aerosil P-25, 100\\u202fmg) and poly(ethylene glycol) (Nacalai Tesque PEG #20000, 10\\u202fmg) in distilled water (0.5\\u202fmL). This solution was mixed with acetylacetone (Wako Pure Chemical Industries, 10\\u202f\\u03bcL) and the surfactant Triton X-100 (Sigma Aldrich, 5\\u202f\\u03bcL) for 30\\u202fmin and was then allowed to stand for\\u202f\\u223c\\u202f24\\u202fh to suppress bubble formation within the solution. The FTO substrates with the TiO2 were annealed at 550\\u202f\\u00b0C for 30\\u202fmin to form the mesoporous TiO2 layer.\\nThe perovskite compounds were prepared by mixing solutions of CH3NH3I (Showa Chemical), HC(NH2)2I (Tokyo Chemical Industries), PbCI2 (Sigma Aldrich), and KI (Wako Pure Chemical Industries), KBr (Wako Pure Chemical Industries), or KCl (Wako Pure Chemical Industries) at 70\\u202f\\u00b0C. All materials were dissolved in N,N-dimethylformamide (DMF; Sigma Aldrich). For comparison purposes, the standard precursor (MA0.90FA0.10PbI3-xXx) was prepared, and had molar concentrations of MAI, FAI, and PbCl2 of 2.16, 0.24, and 0.8\\u202fM, respectively [29]. MA0.8FA0.1 K 0.1PbI3(Cl) precursors, with concentrations of MAI, FAI, K compounds (KI, KBr, or KCl), and PbCI2 of 1.92, 0.24, 0.24 and 0.8\\u202fM, respectively, were prepared. Solutions containing the perovskite precursors were spin-coated on the mesoporous TiO2 layer at 2000\\u202frpm for 60\\u202fs using simultaneous hot air-blowing to obtain highly oriented perovskite crystals [26,30,31]. The temperature of the FTO substrates during hot air-blowing was measured to be 90\\u202f\\u00b0C. Then, the cells were annealed at 150\\u202f\\u00b0C for 20\\u202fmin in ambient air.\\nA hole transport layer (HTL) was formed by spin-coating at 4000\\u202frpm for 30\\u202fs. The HTL precursor solution was prepared by adding 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9\\u2032-spirobifluorene (Sigma Aldrich spiro-OMeTAD, 36.1\\u202fmg) to chlorobenzene (0.5\\u202fmL; Wako Pure Chemical Industries) and by stirring it for 24\\u202fh. A solution of lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI, 260\\u202fmg; Tokyo Chemical Industry) in acetonitrile (0.5\\u202fmL; Nacalai Tesque) was also prepared by stirring it for 24\\u202fh. The former spiro-OMeTAD solution with 4-tert-butylpyridine (14.4\\u202f\\u00b5L; Sigma Aldrich) was mixed with the latter Li-TFSI solution (8.8\\u202f\\u00b5L) for 30\\u202fmin at 70\\u202f\\u00b0C, and cooled to ambient temperature. Finally, a gold (Au) top-electrode was formed by vacuum evaporation.\\nThe J-V characteristics (Keysight B2901A) of the photovoltaic cells were measured when illuminated with a solar simulator (San-ei Electric XES-301S) at 100 mW cm\\u22122 with an air mass (AM) 1.5. The solar cells were illuminated through the side of the FTO substrates, and the exposed area was 0.090\\u202fcm2. The EQEs of the solar cells were also determined by an incident photon-electron conversion efficiency measurement system (Enli Technology QE-R). The microstructures of the perovskite layers were measured using an X-ray diffractometer (Bruker D2 PHASER), while the surface morphologies of the perovskite layers were examined using an optical microscope (Nikon Eclipse E600) and a scanning electron microscope equipped with an EDX detector (JEOL JSM-6010PLUS-LA).\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.1MA0.9PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lithium bis (trifluoromethylsulfonyl) imide (Li-TFSI, 99.95%), 4-tert-butylpyridine (tBP, 96%), and chlorobenzene (99.8%) were purchased from Sigma-Aldrich. Lead iodide (PbI2, 99.999%) and Acetonitrile were provided by Alfa-Aesar. Hydroiodic acid (57\\u00a0wt% in water) and formamidine acetate (99%) were bought from Aladdin. Titanium tetrachloride (TiCl4, 98.0%), anhydrous ethanol, acetone, isopropyl alcohol and anhydrous diethyl ether were purchased from Sinopharm Chemical Reagent Co, Ltd. Formic acid (99%) was purchased from Acros Organics. 2,2,7,7-tetrakis-(N, N-di-p-methoxyphenyl-amine)-9,9-spirobiuorene (spiro-OMeTAD) was bought from Polymer Light Co., Ltd. All materials were used without further purification. HC(NH2)2I (FAI) and CH3NH3I (MAI) powders were synthesized according to the literature .\\n\\nThe TiO2 layer was deposited onto cleaned FTO (coated fluorine doped tin oxide) according to the literature . The FTO/TiO2 substrate was further annealed at 200\\u00a0\\u00b0C for 30\\u202fmin in air. Before perovskite film deposition, the FTO/TiO2 was treated in ultraviolet ozone (Ultraviolet Ozone, Jelight Company) for 15\\u202fmin.\\n\\nFAPbI3 precursor solutions were prepared by dissolving 255\\u202fmg FAI and 693\\u202fmg PbI2 into 1\\u202fmL mixed solvent of \\u03b3-butyrolactone (GBL) and dimethylsulfoxide (DMSO) (7/3, v/v) with different amounts of the formic acid additive, corresponding to the formic acid concentrations from 0\\u202fM to 1.009\\u202fM, followed by stirring at 60\\u00a0\\u00b0C for 2\\u202fh. The solutions without and with formic acid were then spin-coated onto the TiO2/FTO substrate by a two-step spin-coating process at 1000 and 4000\\u202frpm for 10 and 40\\u202fs, respectively. During the second spin-coating step, 180\\u00a0\\u00b5L chlorobenzene was dropped onto the wet film to facilitate the crystallization of perovskite. Then, the obtained wet film was heated at 150\\u00a0\\u00b0C for 30\\u202fmin. For MAPbI3 thin film deposition, the same spin-coating process was applied. 190\\u202fmg MAI and 555\\u202fmg PbI2 as solute in the same mixed solvent and formic acid as additive formed the precursor solutions. The resulted MAPbI3 films, were heated at 100\\u00a0\\u00b0C for 10\\u202fmin.\\n\\nThe spiro-OMeTAD solution was prepared according to the literature . HTL was deposited onto the perovskite film by spin-coating the spiro-OMeTAD solution at 5000\\u202frpm for 30\\u202fs.\\n\\nAn 80-nm-thick gold coating was deposited on the top of the HTL by thermal evaporation. The active cell area of 0.09\\u00a0cm2 was defined by the metallic mask used during the Au deposition.\\n\\n\\nThe dynamic light scattering (DLS) and zeta potential measurement of the perovskite precursor solutions were performed using Brookhaven 90Plus Particle Size and PALS Zeta Potential Analyzer. The J\\u2013V curves of the perovskite solar cells were recorded using a Keithley 2400 source meter under simulated solar illumination. The power output of the solar simulator (AM 1.5\\u202fG, 100\\u202fmW/cm2) was calibrated using a silicon reference cell. The incident photon-to-current efficiency (IPCE) was measured on a QTest Station 500TI system (Crowntech, Inc.). The steady\\u2013state photoluminescence measurement of perovskite film was performed using a PicoQuant FT-300, with 510\\u202fnm excitation wavelength. In situ microscopy images of the crystallization process of FAPbI3 film fabricated from the solutions with and without formic acid were recorded by optical microscope (Olympus BX51) equipped with Heating and Cooling Stage (Linkam LTSE420). Scanning electron microscopy (SEM) images were obtained using a field emission scanning electron microscope (FESEM, SU-8020; Hitachi) with an accelerating voltage of 3\\u202fkV. X-ray diffraction (XRD) spectra were recorded by an X-ray diffractometer (DX-2700) via Cu K\\u03b1 radiation with \\u03bb\\u00a0=\\u00a01.54\\u202f\\u00c5. A Lambda 950 (Perkin-Elmer) was used to investigate the light absorption properties of the perovskite films.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: Formic acid,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2, 99.999%), N,N-dimethylformamide (DMF, 99.8%), dimethyl sulfoxide (DMSO, \\u226599.9%), methylamine (33 wt% in absolute ethanol), hydroiodic acid (57 wt% aqueous solutions), Pb(SCN)2 (99.5%), Li-bis-(trifluoromethanesulfonyl)imide (Li-TFSI) (99.95%), 4-tert-butylpyridine (96%), and acetonitrile (99.8%) were purchased from Sigma-Aldrich. SnO2 dispersion (15 wt% in H2O) was purchased from Thermo Fisher. 2,2\\u2032,7,7\\u2032-Tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (Spiro-OMeTAD) was purchased from Lumtec. All salts and solvents were used as received without any further purification.\\n\\nMethylammonium iodide (CH3NH3I, MAI) was prepared by mixing 18\\u00a0mL of methylamine (33 wt% in absolute ethanol) and 10\\u00a0mL of hydroiodic acid (57 wt% aqueous solution) in a 50-mL three-necked flask at 0\\u00b0C under stirring for 2\\u00a0hr. The CH3NH3I raw precipitate was then collected after evaporation at 50\\u00b0C for 1\\u00a0hr, which was then washed with diethyl ether several times and finally dried at 60\\u00b0C in a vacuum oven for 24\\u00a0hr.\\n\\nThe MAPbI3 precursor solution was prepared by dissolving 461\\u00a0mg of PbI2 and\\u00a0159\\u00a0mg of CH3NH3I in the mixture of 600\\u00a0mg of DMF and 78\\u00a0mg of DMSO. MAPbI3 precursor solution (40\\u00a0\\u03bcL) was dropped onto the substrates with an area of 2\\u00a0cm \\u00d7 2\\u00a0cm, and an air blade was employed to coat the precursor. The nozzle slot width was 1\\u00a0mm and the length 10\\u00a0cm. The distance between the air blade and the solution surface was 4\\u00a0mm. The angle between the nozzle and the substrate was kept at 45\\u00b0, and the speed to move the air blade was kept constantly at 0.5\\u00a0cm s\\u22121. The input N2 flow pressure was adjusted in the range from 0.2 MPa to 0.6 MPa. The coated films were then annealed for 10\\u00a0min at 100\\u00b0C on a hot plate to achieve perovskite films. In this study, the volume of precursor solution used in the air-blading process is exactly same as that in the control SA process for better comparison. Actually our experiments indicated that the lesser precursor solution such as 25\\u00a0\\u03bcL was adequate to produce the perovskite films in an area of 2\\u00a0cm \\u00d7 2\\u00a0cm with similar device performance via the air-blading process. The higher material yield should be achievable for the air-blading process by optimizing the input air-flow pressure, the structure of the air blade, or the distance between the nozzle and the substrate.\\n\\nThe MAPbI3 precursor solution was prepared as mentioned above. The MAPbI3 films were deposited by spin-coating 40\\u00a0\\u03bcL of precursor solution using a spin speed of 4,000\\u00a0rpm for 30\\u00a0s with acceleration of 4,000\\u00a0rpm. Chlorobenzene (180\\u00a0\\u03bcL) was dripped onto the surface of the MAPbI3 film \\u223c5\\u00a0s after commencing spin-coating. The coated films were then annealed for 10\\u00a0min at 100\\u00b0C on a hot plate to achieve perovskite films.\\n\\nITO-coated glass substrates (7\\u00a0\\u03a9 sq\\u22121) were cleaned with water, ethanol, acetone, and isopropyl alcohol in an ultrasonic bath, and subsequently treated in a UV-ozone cleaner for 10\\u00a0min. The transmittance of ITO-glass is \\u223c91.2% and the reflectance is <6.5%. The reflectance of the final PV device is <3.5%. For the air-bladed devices, the compact SnO2 layer was deposited onto the UV-treated ITO substrate by air-blading 40\\u00a0\\u03bcL of SnO2 dispersion (3.75 wt% in H2O) with an input N2 flow pressure of 0.4 MPa, followed by calcination at 150\\u00b0C for 10\\u00a0min in air. The MAPbI3 layer was then deposited via air blading with the required gas pressure as mentioned above.\\u00a0Then 40\\u00a0\\u03bcL of Spiro-OMeTAD solution (72.3\\u00a0mg of Spiro-OMeTAD, 28.8\\u00a0\\u03bcL of 4-tert-butylpyridine, and 17.6\\u00a0\\u03bcL of Li-TFSI solution [520\\u00a0mg of Li-TFSI in 1\\u00a0mL of acetonitrile] solved in 1\\u00a0mL of chlorobenzene) was coated as HTL via the air-blading technique with an input N2 flow pressure of 0.6 MPa. Finally, 80\\u00a0nm of Au was thermally evaporated as a top electrode to finish the device fabrication. For the spin-coated devices, the SnO2 layer was deposited onto the UV-treated ITO substrate by spin-coating 40\\u00a0\\u03bcL of SnO2 dispersion (3.75 wt% in H2O) at 3,000\\u00a0rpm for 30 s, followed by annealing at 150\\u00b0C for 10\\u00a0min in air. The MAPbI3 layer was then deposited via SA process as mentioned above. For the HTL, 40\\u00a0\\u03bcL of Spiro-OMeTAD solution was then spin-coated onto the perovskite layer at 4,000\\u00a0rpm for 30 s. Thereafter, Au was thermally evaporated by following the procedures described above. The preparation of the SnO2 layers was performed in air and the preparation of perovskite films and Spiro-OMeTAD films was performed in a glovebox.\\n\\nSEM images were obtained using Hitachi S-4800 and SU-8020. AFM images were obtained with Bruker Demension Icon. The steady-state PL and TRPL spectra were measured in an Edinburgh Instrument FLS 980. XRD measurements were carried out on a PANalytical Empyrean Powder X-ray diffractometer using CuK\\u03b1 radiation. The ultraviolet-visible (UV-vis) absorption spectra of the perovskite films were collected on a UV-vis spectrophotometer (UH4150, Hitachi). An Oriel Sol3A Class AAA solar simulator (450W Model 94023A, Newport) with an AM 1.5 solar spectrum filter was used as the irradiation source, which was calibrated against a reference cell before each measurement. A monocrystalline silicon reference cell with an area of 2\\u00a0cm \\u00d7 2\\u00a0cm (SRC-1000-TC-QZ) purchased from VLSI Standards was used as the reference cell. Photocurrent density-voltage (J-V) measurements were carried out using Keithley 2420 at room temperature and ambient conditions. The EQE spectrum was measured using a Solar Cell Spectral Response Measurement System QE-R3011 (Enlitech). The light intensity at each wavelength was calibrated using a standard single-crystal Si photovoltaic cell.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Pb(SCN)2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Dropcasting,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I was synthesized by reacting 24\\u00a0mL of methylamine (33wt% in ethanol) and 10\\u00a0mL of hydroiodic acid (57\\u00a0wt% in water, Aladdin reagent, Shanghai, China), and 100\\u00a0mL ethanol in a 250\\u00a0mL round bottom flask under argon at 0\\u00a0\\u00b0C for 2\\u00a0h with stirring. After reaction, the white precipitate of CH3NH3I was recovered by rotary evaporation at 50\\u00a0\\u00b0C and then dissolved in ethanol followed by sedimentation in diethyl ether by stirring the solution for 30\\u00a0min. This step was repeated three times and the white CH3NH3I powder was finally collected and dried at 50\\u00a0\\u00b0C in a vacuum oven overnight. PbI2 was also purchased from Aladdin reagent. The PEDOT:PSS aqueous solution (Clevios PVP Al4083) and PCBM was purchased from H. C. Starck (Leverkusen, Germany) and American Dye Sources, Inc. (Baie-d'Urf\\u00e9, Quebec, Canada). The above materials were used as received. ITO glass substrates with a sheet resistance of 15\\u00a0\\u03a9/sq were obtained from Shenzhen Display (Shenzhen, China).\\n\\nITO glass was cleaned in an ultrasonic bath with detergent, ultrapure water, acetone, and isopropyl alcohol for 20\\u00a0min, respectively. After being treated in an oxygen plasma for 6\\u00a0min, a thin layer of PEDOT:PSS (30\\u00a0nm) was spin-coated onto the ITO glass with a speed of 4000\\u00a0rpm and baked at 150\\u00a0\\u00b0C for 20\\u00a0min. To form the stoichiometric CH3NH3PbI3 precursor solution, the CH3NH3I and PbI2 (1\\u00a0M) were dissolved in a mixture of anhydrous GBL: DMSO (7:3), with 5 v/v% NMP. Solutions were heated at 70\\u00a0\\u00b0C overnight to encourage dissolution of solid material, cooled to room temperature, and then filtered with a 0.22\\u00a0\\u03bcm PTFE filter before use. Then, the precursor solution was spin-coated onto the PEDOT:PSS modified ITO glass at 4000\\u00a0rpm for 50\\u00a0s. During the spin coating, toluene was used to wash the surface to form high-quality surface coverage, as reported by Seok. After being thermal treated at 90\\u00a0\\u00b0C for 20\\u00a0min in a glovebox, a thin layer of PCBM (50\\u00a0nm) was spin-coated onto the surface of perovskite layer in a 15\\u00a0mg\\u00a0mL\\u22121 chlorobenzene solution at a speed of 1500\\u00a0rpm. The devices were completed after thermal deposition of 10\\u00a0nm calcium and 100\\u00a0nm aluminum as the cathode at a pressure of 4\\u00a0\\u00d7\\u00a010\\u22124\\u00a0Pa. The detailed device configuration and the SEM cross-section image of the optimized perovskite solar cells are given in Fig.\\u00a0S1 (Supporting information). The device area was 10\\u00a0mm2 for each cell defined by shadow mask.\\n\\nThe X-ray diffraction (XRD) pattern was obtained on a Bruker D8 ADVANCE (Billerica, MA). The absorption spectra of the films on ITO glass were observed by a scanning spectrophotometer (Varian Cary 50 UV/vis, Palo Alto, CA) in the range of 250\\u2013800\\u00a0nm. Surface morphological characterizations of the films were characterized by a tapping-mode atomic force microscope (AFM, Agilent 5400, Keysight Technologies, Santa Rosa, CA) and scanning electron microscopy (SEM, Hitachi S-4800). The thicknesses of the films were measured by Veeco Dektak 150 surface profiler. Current density\\u2013voltage (J\\u2013V) characteristics of the devices were measured with a Keithley 2420 source measurement unit (Cleveland, OH)under the illumination of AM 1.5G, 100\\u00a0mW\\u00a0cm\\u22122 with a Newport solar simulator (Irvine, CA). Light intensity was calibrated with a standard silicon solar cell. Stability of the PSCs was explored, and the unencapsulated devices were stored in glovebox and periodically tested. The J\\u2013V curves were measured by reverse scan (from bias 1.0\\u00a0V to\\u00a0\\u2212 0.1\\u00a0V) and the step voltage was fixed at 10\\u00a0mV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL; NMP,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ca | Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 480,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"MAI (methylammonium iodide) was synthesized by reacting 50\\u00a0mL hydriiodic acid (57% in water, Aldrich) and 50\\u00a0mL methylamine (40% in methanol, Junsei Chemical Co. Ltd.) in a 250\\u00a0mL round-bottom flask at 0\\u00a0\\u00b0C for 2\\u00a0h with magnetically stirring. The white precipitates were recovered by evaporation at 50\\u00a0\\u00b0C for 1\\u00a0h with a rotary evaporator. The products were dissolved in ethanol and recrystallized from diethyl ether to purify MAI. Finally the products were dried at room temperature in a vacuum oven for 24\\u00a0h.\\nTo obtain MAPbI3\\u2212xClx perovskite powder, MAPbI3\\u2212xClx perovskite solution was prepared by mixing the MAI powder and PbCl2 (Junsei Chemical Co. Ltd.) powder with 40\\u00a0wt% 3:1\\u00a0M ratio in N,N-dimethylformamide (DMF) at 60\\u00a0\\u00b0C for 30\\u00a0min. This solution was dropped on a 20\\u00a0cm\\u00a0\\u00d7\\u00a020\\u00a0cm glass plate and was spread by a bar (or a blade). The spread solution on a glass plated was then dried and subsequently heat-treated at each temperature (100, 125, 150, and 175\\u00a0\\u00b0C) for 30\\u00a0min under air atmosphere. The MAPbI3\\u2212xClx perovskite powders were obtained by raking the as-heated black film with slide glass. To collect sufficient MAPbI3\\u2212xClx perovskite powder, this process was repeated several times.\\n\\nTo fabricate the planar MAPbI3\\u2212xClx perovskite solar cell, dense TiO2 blocking layer (bl-TiO2) of 50\\u00a0nm-thickness was deposited on a cleaned F-doped SnO2 (FTO, Pilkington, TEC8) glass substrate by spray pyrolysis deposition of 20\\u00a0mM of titanium diisopropoxide bis(acetylacetonate) (Sigma-Aldrich) solution at 450\\u00a0\\u00b0C. To form uniform MAPbI3\\u2212xClx perovskite layer on bl-TiO2/FTO substrate, the 40\\u00a0wt% as-prepared MAPbI3\\u2212xClx perovskite powder were dissolved in dimethyl sulfoxide (DMSO) at 60\\u00a0\\u00b0C for 30\\u00a0min under magnetic stirring. The 40\\u00a0wt% MAPbI3\\u2212xClx perovskite/DMSO solution was dropped on bl-TiO2/FTO substrate and was then spin-coated at 2000\\u00a0rpm for 60\\u00a0s and at 4000\\u00a0rpm for 30\\u00a0s under air condition. The spin-coated MAPbI3\\u2212xClx perovskite/bl-TiO2/FTO substrate was then dried at 100\\u00a0\\u00b0C for 2\\u00a0min. To form conventional MAPbI3\\u2212xClx perovskite layer, 40\\u00a0wt% MAI:PbCl2 (3:1\\u00a0M ratio) solution was prepared by mixing the 3:1 MAI:PbCl2 powder in DMSO solution. The 40\\u00a0wt% 3:1 MAI:PbCl2 solution was spin-coated on bl-TiO2/FTO substrate at 2000\\u00a0rpm for 60\\u00a0s and at 4000\\u00a0rpm for 30\\u00a0s under air condition and was then heated at 100\\u00a0\\u00b0C for 40\\u00a0min. A poly(triaryl amine) (PTAA, EM index) hole conductor was deposited on the each MAPbI3\\u2212xClx perovskite/bl-TiO2/FTO substrate by spin coating PTAA/toluene (15\\u00a0mg/mL) solution with Li-bis(trifluoromethanesulfonyl)imide (Li-TFSI)/acetonitrile (7.5\\u00a0\\u03bcL, 170\\u00a0mg/mL) and tBP/acetonitrile (7.5\\u00a0\\u03bcL, 1:1) additives at 2000\\u00a0rpm for 30\\u00a0s. Finally, the Au counter electrode was deposited by thermal evaporation. The active area was fixed as 0.16\\u00a0cm2. All device fabrication was conducted below relative humidity of 35%.\\n\\nThe external quantum efficiency (EQE) was measured by using a power source (150\\u00a0W Xenon lamp, 13014, ABET) with a monochromator (MonoRa-500i, Dongwoo Optron Co., Ltd) and a potentiostat (IviumStat, IVIUM). The current density-voltage (J-V) curves were measured by a solar simulator (PEC-L01, Peccell) with a potentiostat (IviumStat, IVIUM) at 100\\u00a0mA\\u00a0cm\\u22122 illumination AM 1.5G and a calibrated Si-reference cell certificated by JIS (Japanese Industrial Standards). For the measurement hysteresis of J-V curves with respect to the scan direction, the scan rate (\\u0394V\\u00b7(delay time)\\u22121) was set to 10\\u00a0mV\\u00b7200\\u00a0ms\\u22121 as a standard condition and was varied from 10\\u00a0mV\\u00b7100\\u00a0ms\\u22121 to 10\\u00a0mV\\u00b71000\\u00a0ms\\u22121. The J-V curves of all devices were measured by masking the active area with metal mask of 0.096\\u00a0cm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Flexible ITO films were sputtered at room temperature on a CPI and PET substrates with a width of 150\\u00a0mm using a lab-scale RTR sputtering system, respectively . The CPI substrates were supplied by Kolon Industries, Inc. Prior to sputtering, the flexible substrates of both types were irradiated with an Ar ion beam operated at a direct current (DC) pulsed power of 200\\u00a0W. After surface treatment of the flexible substrates, 100\\u00a0nm-thick ITO films were sputtered onto each substrate using rectangular ITO target at a constant direct current (DC) power of 550\\u00a0W, a working pressure of 1 mTorr, an Ar/O2 flow ratio of 30/1 sccm, and a rolling speed of 1.05\\u00a0cm/s.\\nFig.\\u00a01 (a) schematically illustrates the RTR sputtering process for fabricating an ITO film on a 150\\u00a0mm-wide CPI or PET substrate at room temperature. After RTR sputtering, the ITO films on the CPI substrate were subjected to rapid thermal annealing (RTA) at 300\\u00a0\\u00b0C for 10\\u00a0min to improve the electrical and optical properties of the ITO. Fig.\\u00a01(b) show the picture of the highly flexible and transparent ITO/CPI substrate after RTA process.\\n\\nThe electrical and optical properties of the RTR-sputtered ITO/CPI and ITO/PET samples were examined using Hall measurements (HL5500PC) and UV/visible spectrometry (UV 540). The mechanical properties of the ITO/CPI and ITO/PET samples were evaluated using a specially designed inner and outer bending system. The outer bending test induced tensile stresses on the film, whereas the inner bending test induced compressive stresses. The change in resistance of the ITO films due to substrate bending can be expressed as \\u0394R (=R\\u00a0\\u2212\\u00a0R0)/R0, where R0 is the initial measured resistance, and R is the resistance measured under substrate bending. The following equation was used to calculate the peak strain for a curved ITO film with decreasing bending radius : Strain=dITO+dSub2R\\u00d7100 where, d ITO and d Sub are the thicknesses of the ITO and the flexible substrate, respectively. In addition, dynamic fatigue bending was performed using a cyclic bending test machine designed in house and operated at the frequency of 0.5\\u00a0Hz for 10,000 cycles.\\n\\nThe ITO/PET and ITO/CPI substrates were cleaned by ultrasonication in 5% Helmanex soap in de-ionized water, ethanol, and then isopropyl alcohol. After solvent cleaning, the substrates were treated with an Ar plasma (150\\u00a0W) to remove the organic residues. The ZnO nano-sol used to fabricated ZnO electron conductor, was prepared by a reported method . Briefly, 1.64\\u00a0g zinc acetate dehydrate (Aldrich) and 0.5\\u00a0g ethanolamine (Aldrich) were dissolved in 10\\u00a0g 2-methoxyethanol (Aldrich) under vigorous stirring at 60\\u00a0\\u00b0C for 30\\u00a0min. The ZnO nano-sol solution was then spin-coated onto cleaned ITO/PET and CPI substrates at 2000\\u00a0rpm for 60\\u00a0s and then dried at 150\\u00a0\\u00b0C for 10\\u00a0min. A 40\\u00a0wt % solution of MAPbI3 perovskite was prepared by mixing MAI (DS Logics. Co., Ltd.) and PbI2 (Aldrich) in a 1:1\\u00a0M ratio in a N,N-dimethylformamide (DMF, Aldrich) at 60\\u00a0\\u00b0C for 30\\u00a0min, and hydriodic acid was added to the MAPbI3 perovskite solution. The 40\\u00a0wt % of MAPbI3 perovskite solution with hydriodic acid (40\\u00a0wt% MAPbI3 in DMF solution/hydriodic acid\\u00a0=\\u00a01\\u00a0mL/100\\u00a0\\u03bcL) was then spin coated onto the ZnO/ITO/PET or CPI substrates at 3000\\u00a0rpm for 200\\u00a0s and then dried on a hot plate at 100\\u00a0\\u00b0C for 2\\u00a0min. Afterwards, a poly-triarylamine (PTAA, EM index Co., Ltd.) hole conductor with additives was deposited on the MAPbI3/ZnO/ITO/PET and CPI substrates by spin-coating a mixture of PTAA/toluene (15\\u00a0mg/1\\u00a0mL) with 7.5\\u00a0\\u03bcL Li-bis (trifluoromethanesulfonyl) imide (Li-TFSI, Aldrich)/acetonitrile (170\\u00a0mg/1\\u00a0mL) and 7.5\\u00a0\\u03bcL tert-butylpyridine (t-BP, Aldrich)/Acetonitrile (1\\u00a0mL/1\\u00a0mL) additives at 3000\\u00a0rpm for 30\\u00a0s. Finally, an Au counter electrode was deposited by thermal evaporation. The active area was fixed at 0.16\\u00a0cm2. All device fabrications were conducted under relative humidity conditions below 25%.\\n\\nCurrent density-voltage (J-V) curves were measured using a solar simulator (Peccell, PEC-L01) equipped with a potentiostat (IVIUM, IviumStat), under 1 sun equivalent illumination (100\\u00a0mW/cm2 AM 1.5G), calibrated using a Si-reference cell certified by Japanese Industrial Standards. The J-V curve for each device was acquired by masking the active area with a metal mask of 0.096\\u00a0cm2. The external quantum efficiency (EQE) was measured using a power source (ABET 150\\u00a0W xenon lamp, 13014), a monochromator (DONGWOO OPTORN Co., Ltd., MonoRa-500i), and a potentiostat (IVIUM, IviumStat).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: Polyimide | ITO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: HI,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.096,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The PbI2-DMSO@DMF precursor solution was prepared by dissolving both the PbI2 (99.9985%, Alfa Aesar) and DMSO (purity 99.9%, Sigma-Aldrich) into DMF (purity 99.8%, Sigma-Aldrich) at the ratio of 1.3\\u202fmol/L. The methyl ammonium iodide (MAI, >99.5%, Xi\\u2019an Polymer Light Technology Corp) of 60\\u202fmg was dissolved into 1\\u202fmL isopropyl alcohol (IPA, Aladdin) to form the ultrahigh concentration (0.337\\u202fmol/L) MAI/IPA solution. The [,]-phenyl-C61-butyric acid methyl ester (PCBM, Xi\\u2019an Polymer Light Technology Corp) of 30\\u202fmg was dissolved into 1\\u202fmL Chlorobenzene (Sigma-Aldrich). A saturated bathocuproine (BCP, Xi\\u2019an Polymer Light Technology Corp) /IPA precursor solution was obtained by adding excess BCP into 1\\u202fmL IPA at temperature of 25\\u202f\\u00b0C.\\n\\nThree different NiOx thin films were sputtered on fluorine-doped tin oxide (FTO) substrates without intentional heating using a Denton Vacuum DESKTOP PRO sputter deposition system (Denton Vacuum LLC). Two of them were deposited by reactive DC/RF magnetron sputtering techniques from an Ni target (50\\u202fmm in diameter and 3\\u202fmm in thickness) and the other was deposited by DC magnetron sputtering from an NiO target (atomic ratio: 1:1, 50\\u202fmm in diameter and 3\\u202fmm in thickness, binding with 3\\u202fmm-thickness copper backplane). Both of the Ni target and NiO target were of high purity (99.99%). Prior to the sputtering of each film, the base pressure in the chamber was pumped down to less than 1E-6\\u202fTorr. The target was pre-sputtered for 15\\u202fmin to remove the contamination layer if any on the surface of the target. Over all these three sputtering operations, pure oxygen was introduced as the sputtering gas. The total sputtering pressure and power were constantly kept at 1E-2\\u202fTorr and 100\\u202fW, respectively (see Table 1 ). The distance between the target and substrates was approximately 8\\u202fcm. All the films were obtained at room temperature and their thickness were controlled through tuning the deposition time.\\nFor comparison, devices with PEDOT:PSS electrode interlayer were also prepared. PEDOT: PSS was spin-coated (2000\\u202frpm, 30\\u202fs) on pre-cleaned FTO/glass and subsequently heated at 150\\u202f\\u00b0C for 20\\u202fmin in air condition.\\n\\nThe planar-heterojunction hybrid PSCs were fabricated in standard arrangement by sandwiching a planar layer of CH3NH3PbI3 between the NiOx hole transport layer and the PCBM electron transport layer. The counter layer was made of a bathocuproine (BCP) exciton blocking film and silver (Ag). Prior to the device fabrication, the pre-patterned FTO/glass substrates (NSG Corp, 14\\u202f\\u03a9/sq) were rinsed with detergent and then sequentially ultrasonic cleaned in de-ionized water, acetone and ethanol.\\nAfter depositing the NiOx layers, the methyl ammonium lead iodide (CH3NH3PbI3) layer was prepared using a continuous dripping method which had been detailed described in our previous work []. Briefly, substrates loaded with 30\\u202f\\u03bcL PbI2-DMSO@DMF precursor solution were set to spin at 4000\\u202frpm for totally 45\\u202fs and the MAI/IPA solution was dripped on the spinning substrates at the 25th\\u202fs. To ensure PbI2 completely transform into MAPbI3, the samples were heated on a hot plate at 120\\u202f\\u00b0C for 20\\u202fmin. Subsequently, both the PCBM/chlorobenzene and the saturated BCP /IPA precursor solutions were spin-coated at 2000\\u202frpm for 25\\u202fs after a filter process. All these procedures were implemented inside an Argon-filled glove box at 25\\u202f\\u00b0C. Finally, the Ag electrode was thermally deposited on the BCP layer inside a vacuum chamber (<1E-6\\u202fTorr) through a shadow mask and the active area of PSC devices was 0.09\\u202fcm2.\\n\\nThe current density-voltage (J\\u2013V) characteristics of devices were measured using a Keithley 2400 digital source meter under simulated AM 1.5\\u202fG solar irradiation at 100\\u202fmW/cm2 in ambient condition. The J\\u2013V characteristics were recorded by reverse and forward scan in the range from \\u22120.1\\u202fV to +1.2\\u202fV with a scan rate of 50\\u202fmV/s. XRD results were acquired using a Rigaku Utima IV XRD system. Transmittance and absorbance measurements were carried out by Shimadzu UV-2550. Field emission scanning electron microscope (SEM) images were obtained using SUPRA 55 FESEM system. X-ray photoelectron spectroscopy (XPS) data were obtained using XPS ESCALAB 250, the C 1\\u202fs peaks were calibrated at 254.8\\u202feV. The Valance band (VB) spectra were measured with a monochromatic He I light source (21.21\\u202feV) and a VG Scienta R4000 analyzer. A sample bias of \\u22125\\u202fV was applied to observe the secondary electron cutoff (SEC). Photoluminescence (PL) measurements were carried out by Hitachi F7000 fluorescence spectrometer. The electronic impedance spectroscopy (EIS) test of the devices was carried out without illumination in the range from 100\\u202fHz to 1\\u202fMHz using EG&G VersaSTAT 3. All the characterized NiOx samples were deposited on FTO substrates, their thicknesses were controlled to be 100\\u202fnm for XRD analysis and 50\\u202fnm for XPS and UPS analysis.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 120.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 20.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 936,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 40,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO glass (Pilkington, NSG TEC-15) was cleaned with detergent, facilitated by ultrasonication in water, acetone and iso-propanol baths successively before deposition of SnO2 ESLs. The SnO2 layer was deposited on the FTO substrates as reported previously. Plasma-enhanced atomic layer deposition (PEALD) process was done with an equipment of Ensure Scientific Group AutoALD-PE V2.0 equipped with a plasma generator. Tetrakis(dimethylamino)-tin(IV) (99%, TDMA-Sn, Strem Chemicals Inc.) was used as the Sn precursor. Oxygen and Argon are used as oxidizer and carrier gases, respectively. The temperature of the reaction is fixed at 100 \\u00b0C during the deposition process.\\n\\nLead iodide (PbI2, Alfa Aesar, 99.9985%), methylammonium iodide (MAI, Dyesol), formamidinium iodide (FAI, Dyesol), lead thiocyanate (Pb(SCN)2, Sigma-Aldrich, 99.5%), dimethyl sulfoxide (DMSO, Sigma-Aldrich, 99.8%) and N,N-dimethylformamide (DMF, Sigma-Aldrich, 99.8%) are purchased and used without further purification. The perovskite precursor was prepared using a Lewis acid-base adduct approach with the mixture of MAI, FAI, PbI2, and DMSO in DMF, where the molar ratio of DMSO and PbI2 is 1:1 . A 45% by weight precursor solution of MAPbI3 was prepared with PbI2, MAI and DMSO (molar ratio=1:1:1) in DMF. The solution was stirred for 12 h on a 60 \\u00b0C hot plate before deposition. The FAPbI3 precursor solution was made in the same process. The MA1\\u2212xFAxPbI3 precursor was prepared by mixing two different solutions together with different volume ratio, where the ratio of MAI and FAI is changed from 1:0 to 0:1 (x=0, 0.2, 0.3, 0.4, 0.6, 0.8, 1.0). The resulting mixed precursor solution was stirred for one hour on a 60 \\u00b0C hotplate and then purified using a 0.45 \\u00b5m filter before spin-coating.\\nThe precursors with Pb(SCN)2 additives are prepared with fixed amounts of Pb(SCN)2 with respect to the weight of PbI2, where the content of Pb(SCN)2 ranging from 0% to 5%.\\n\\nC60-SAM was deposited on PEALD SnO2 as previously reported . The perovskite precursor solution was spin-coated on the ESL first at 500 rpm for 3 s, and then at 4000 rpm for 60 s using a fast deposition-crystallization technique with diethyl ether as the anti-solvent agent. After spin coating, the perovskite film was annealed at 65 \\u00b0C for 2 min and then 100 \\u00b0C for 5 min. All of these processes were carried out in a N2 filled glove box.\\n2,2\\u2032,7,7\\u2032-tetrakis(N,N\\u2032-di-p-methoxyphenylamine)\\u22129,9\\u2032-spirobifluorene (Spiro-OMeTAD) was used as the HSL and deposited on the perovskite film at 2000 rpm for 60 s. The Spiro-OMeTAD was co-doped using Co-TFSI and Li-TFSI. The Spiro-OMeTAD solution was prepared by dissolving 72.3 mg Spiro-OMeTAD (Shenzhen Feiming Science and Technology Co., Ltd., 99.0%) in 1 mL chlorobenzene (CB) with 28 \\u03bcL 4-tert-butylpyridine (TBP) (Sigma-Aldrich, 96%), 18 \\u03bcL Li-bis-(trifluoromethanesulfonyl) imide (Li-TFSI) (Sigma-Aldrich, 99.95%) (520 mg/mL in acetonitrile) and 18 \\u03bcL Co(II)\\u2013TFSI salt (FK102, Dyesol) (300 mg/mL in acetonitrile). A layer of 80 nm gold (Au) was then deposited on the top of Spiro-OMeTAD using thermal evaporation. The working area of the devices was 0.08 cm2 as defined by a shadow mask during the Au evaporation.\\n\\nJ-V curves were measured using a Keithley2400 sourcemeter under standard AM 1.5 G illumination using solar simulator (PV Measurements Inc.) with an output intensity of 100 mW/cm2. For light intensity dependence test, the light intensity was later adjusted between 1 and 100 mW/cm2 using neutral density filters. EQE measurement was carried out with an EQE system (PV Measurements Inc,) using 100 Hz chopped monochromatic light ranging from 300 nm to 900 nm under otherwise near-dark test conditions. The top-view and cross section structures of perovskite films and PVSCs were characterized with a field emission SEM instrument (Hitachi S-4800). Crystallinity and the crystal structure of the perovskite layer were analyzed with an Ultima III X-ray Diffractometer using a Ni-filtered Cu K\\u03b1 x-ray source (Rigaku Corp.). Absorbance spectra were obtained with a UV\\u2013vis spectrophotometer (PerkinElmer Lambda 1050). Sheet resistance was measured using four-point probe method resistivity test system (PRO4-440N, Lucas labs). For steady-state photoluminescence (PL) and time resolved photoluminescence (TRPL) measurements, perovskite films were fabricated by spin-coating perovskite precursors on glass substrates followed by coating another encapsulating layer of polymethylmethacrylate (PMMA) after thermal annealing. PL measurements were performed in ambient air at room temperature. Samples were illuminated through the film side. A 532 nm continuous-wave laser (beam diameter \\u224890 \\u00b5m) at 40 mW/cm2 was used as an excitation wavelength for steady-state PL measurement. PL signal was detected via Symphony-II CCD (from Horiba) detector after a 300 g mm\\u22121 grating monochromator (Integration time =0.5 s). For TRPL measurements, samples were excited by a 532 nm pulsed laser (pulse width =5 ps, beam diameter \\u2248150 \\u00b5m) at 1010 photons pulse\\u22121 cm\\u22122. TRPL measurements were performed with time correlated single photon counting (TCSPC) module (Becker & Hickel Simple Tau SPCM 130-E/M module) and the radiative recombination events were detected (Integration time =600 s) via hybrid APD/PMT module (R10467U-50). PL decays of perovskite films with x=0.3, 0.4, 0.6 and 0.8 are single exponential while bi-exponential PL decays are observed in case of x=0, 0.2 and 1.0. In case of bi-exponential PL decay, the photoluminescence intensity contribution of each component is proportional to the product of amplitude (Ai) and lifetime (\\u03c4i). Therefore, the intensity average lifetime of bi-exponential PL decay is calculated as Meanlifetime(\\u03c4)=A1\\u03c412+A2\\u03c422A1\\u03c41+A2\\u03c42\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c | C60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: ALD | Spin-coating,\\n Perovskite_composition_long_form: FA0.3MA0.7PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: Pb(SCN)2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65; 100,\\n Perovskite_deposition_thermal_annealing_time: 2.0; 5.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Chemicals: Cesium Bromide (CsBr, TCI), lead iodide (PbI2, TCI), poly (3-hexylthiophene-2,5-diyl), chlorobenzene (99.99%, TCI), anhydrous N,N-dimethylformamide (DMF, 99.99%, Sigma-Aldrich), anhydrous dimethyl sulfoxide (DMSO, 99.99%, Sigma-Aldrich), SnO2 nanoparticles (15% dispersed in water, Alfa Aesar), Tin (\\u2161) chloride (SnCl2, 99.99%, Sigma-Aldrich), ethanol (99.8%, Sigma-Aldrich), 2-aminothiazole (97%, Sigma-Aldrich), imidazolium iodide (Sigma-Aldrich), hydriodic acid (HI, 57% in H2O).\\nSynthesis of 2-Aminothiazolium Iodide salts (ATI): 2-aminothiazole (10\\u202fmmol, 1\\u202fg) was dissolved in small amount of ethanol and stirred in an ice bath. Then HI solution (15\\u202fmmol, 3.36\\u202fg) was added dropwise to above solution. The mixture was stirred vigorously for 2\\u202fh in ice bath, after evaporation of solvents, the crude product was obtained by diethyl ether wash for 3 times. Then the crude product was purified by recrystallization.\\nDevice fabrication\\ua789 The indium tin oxide (ITO)-coated glass (10\\u202f\\u03a9 sq\\u22121) was sonicated with detergent and then cleaned by a sequential deionized water, acetone and isopropanol for 20\\u202fmin each. Then substrates were treated by UV ozone for 20\\u202fmin to clean the substrate surface. The electron transport layer SnO2 was prepared by spin-coating the diluted SnO2 colloid solution (from 15% to 2.67% in water) on fresh ITO substrates at 2000\\u202frpm for 30s and then annealed at 150\\u202f\\u00b0C for 30\\u202fmin. Then SnCl2 solution (0.1\\u202fM in ethanol) was spin-coated on SnO2 layer at 6000\\u202frpm for 30s and annealed at 180\\u202f\\u00b0C for 1\\u202fh. The SnO2 substrates were treated by oxygen plasma for 5\\u202fmin to make sure the hydrophilicity of substrates. 1.25\\u202fM CsPbI2Br perovskite precursor was prepared by dissolving 576.26\\u202fmg PbI2 and 266.01\\u202fmg CsBr into 1\\u202fml DMF/DMSO mixture (1\\ua7899\\u202fV/V) and stirred overnight. The perovskite film was prepared by a two-step spin-coating procedure at 1000\\u202frpm and 3000\\u202frpm for 10\\u202fs and 30\\u202fs respectively in glove box with \\u02c20.01\\u202fppm H2O and \\u02c250\\u202fppm O2, then the substrates were annealed by sequential 40\\u202f\\u00b0C for 3\\u202fmin and 160\\u202f\\u00b0C for 10\\u202fmin. For delocalized molecules surface treatment, Various concentration of ATI or IAI solutions were prepared by dissolving ATI or IAI in isopropanol (IPA), and then the annealed perovskite film was post-treated by ATI or IAI solutions (100\\u202f\\u03bcl) during the spin-coating (3000\\u202frpm, 30s). Finally, the post-treated film was annealed at 140 for 5\\u202fmin. Pre-heated P3HT solution in chlorobenzene was deposited on perovskite layer at 3000\\u202frpm for 30\\u202fs and annealed at 130\\u202f\\u00b0C for 10\\u202fmin. Finally after cooling down to the room temperature, 80\\u202fnm Au electrode was deposited by thermal evaporation.\\nCharacterization: X-ray diffraction (XRD) patterns were performed by D8 X-ray diffractometer utilizing Cu K\\u0251 radiation. The CsPbI2Br perovskite surface morphologies and the cross-sectional image of the perovskite device were obtained by SEM (HITACHI S4800). Ultravilot-visible absorbance spectra of perovskite films were measured by JASCO-550Uv\\u2013Visible\\u2013near infrared spectrophotometer. The density of state (DOS) was determined using photoelectron yield spectroscopy (PYS), which was performed by Bunkoukeiki KV205-HK ionization energy system.\\nX-ray photoelectron spectroscopy (XPS) was characterized by ESCLAB 250Xi spectrometer and C1s binding energy was referenced at 284.8\\u202feV. The J-V curves of perovskite solar cells were characterized by 100\\u202fmW/cm2 AM 1.5G solar simulator (Bunkouki CEP-2000SRR). Perovskite devices were conducted under forward and reverse scan directions at a rate of 0.01\\u202fV/s. The external quantum efficiencies (EQE) were measured by illuminating solar cells under monochromatic light from 800\\u202fnm to 300\\u202fnm (300\\u202fW Xenon lamp with a monochromator, Newport 74010), calibrated by Si reference solar cell. Electrochemical impedance spectra (EIS) was conducted by an electrochemical workstation (Parstat 2273, Princeton) at a positive bias of 0.6\\u202fV. TPC/TPV were determined by a microsecond pulse of a white light incident without bias light on solar cells under short circuit conditions and open circuit condition.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBrI2,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 40; 160,\\n Perovskite_deposition_thermal_annealing_time: 3.0; 10.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 2,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 15,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"TiO2-sol was synthesized following a previous report .\\nBCP-MAPbI3-xClx perovskite precursor solution synthesis: Varied amounts of BCP (0\\u20131200\\u00a0\\u03bcg/mL) (Sigma-Aldrich, 99.9%) were dissolved in 1\\u00a0mL of DMF (N, N-dimethylformamide) at 80\\u00a0\\u00b0C for 5\\u00a0h on a hotplate, MAI and PbCl2 (Sigma-Aldrich) were added into each BCP solution at a 3:1\\u00a0mol ratio and 30\\u00a0wt%. The precursor solutions were heated at 60\\u00a0\\u00b0C for 12\\u00a0h on a hotplate.\\n70\\u00a0mg/mL solution of Spiro-OMETAD (Xi'an Polymer Light Technology Corp.) hole transport material was prepared in chlorobenzene. 17.6\\u00a0\\u03bcL 4-tert-butylpyridine (4-TBP) and 12.5\\u00a0\\u03bcL bis(trifluoromethane)sulfonimide lithium salt (LiTFSI) (520\\u00a0mg/mL of acetonitrile solution) were then added into the Spiro-OMETAD solution .\\nThe structure of the fabricated solar cell is FTO/TiO2/BCP (x)-MAPbI3-xClx/Spiro-OMETAD/Ag where \\u201cx\\u201d is the density of BCP solution. The device fabrication steps are as follow:\\nFTO-coated glass substrates were successively cleaned with distilled water, EtOH and acetone in an ultrasonic bath. The surfaces of the cleaned FTO-coated glass substrates were treated with oxygen plasma at 50\\u00a0W for 5\\u00a0min. A conductive TiO2 (0.2\\u00a0mol/L) was deposited on the treated FTO-coated glass substrates at 3000\\u00a0rpm for 20\\u00a0s by spin-coating. The films were placed in a muffle furnace at 400\\u00a0\\u00b0C for 30\\u00a0min for complete crystallization. The furnace was allowed to cool to room temperature. The substrates were removed and transferred into a glove box filled with nitrogen. The BCP-MAPbI3-xClx precursor solutions were spin-coated on the TiO2 films at 3500\\u00a0rpm for 30\\u00a0s. The films were left for 20\\u00a0min without heating. Whereafter, the films were annealed at 100\\u00a0\\u00b0C for 60\\u00a0min on a hotplate to ensure the crystallization of MAPbI3-xClx. The Spiro-OMETAD based hole transport material was deposited at 3000\\u00a0rpm for 30\\u00a0s. The films were then put into a drying vessel overnight for the oxidization of Spiro-OMETAD. Finally, silver cathode was thermally evaporated on the Spiro-OMETAD layer at 1\\u00a0\\u00c5/s. The thickness of the silver cathode was 100\\u00a0nm. A device active area of 0.1\\u00a0cm2 was created with a shadow mask during evaporation. Reference devices were also fabricated with the same method.\\n\\nCurrent density-voltage (J-V) and Current density-time data were measured with an AM1.5G solar simulator (100\\u00a0mW\\u00a0cm\\u22122, Sciencetech Inc., SS-150) and a Keithley 2400 source meter, under illumination. The light intensity of solar simulator was calibrated by standard Si solar cell. The external quantum efficiency (EQE) spectra of devices were measured by a certified IPCE instrument (Beijing 7-Star Optical Instruments Co., Ltd.) without bias light. The impedance spectroscopy was measured by a FRA equipped PGSTAT-30 from Autolab. Surface morphologies of MAPbI3-xClx films were characterized with a scanning electron microscope (FEI Quanta 250). The Uv\\u2013vis absorption curve was recorded on a Uv\\u2013visible spectrophotometer (Jasco V-570). X-ray diffraction (XRD) patterns were achieved using a D/max-2400 X-ray diffraction spectrometer (Rigaku, Japan). All measurements were taken in air. All measurements of light intensity were under AM1.5G solar simulator (100\\u00a0mW\\u00a0cm\\u22122, Sciencetech Inc., SS-150).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: BCP; Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The ZnO sol\\u2013gel precursors comprised 1.64\\u202fg zinc acetate dehydrate, 10\\u202fmL 2-methoxyethanol, and 0.5\\u202fmL ethanolamine, and stirred at 60\\u202f\\u00b0C overnight before use. For the ZnO ETL fabrication, the ZnO sol\\u2013gel precursors were spin-coated onto O2 plasma-treated substrates at 3500\\u202frpm for 30\\u202fs, followed by annealing at 150\\u202f\\u00b0C for 10\\u202fmin. The TiCl4 treatment was performed by immersing the ZnO ETLs into a 40\\u202fmM TiCl4 solution at 70\\u202f\\u00b0C for 30\\u202fmin and drying them at 130\\u202f\\u00b0C in air for 30\\u202fmin. Subsequently, PC61BM ([6,6]-phenyl-c61-butyric acid methyl ester) solutions (10\\u202fmg/mL in chlorobenzene) were spin-coated on ZnO ETLs at 2500\\u202frpm for 30\\u202fs and dried at 90\\u202f\\u00b0C for 10\\u202fmin.\\n\\nThe sequential deposition method was applied to fabricate a CH3NH3PbI3 perovskite film onto the substrates. After this, 462\\u202fmg of PbI2 was dissolved in 1\\u202fmL DMF (1\\u202fM) and stirred at 60\\u202f\\u00b0C overnight. The PbI2 solution was spin-coated at 3500\\u202frpm for 30\\u202fs and dried at 70\\u202f\\u00b0C. After drying, the PbI2-deposited ZnO films were immersed in MAI (CH3NH3I) solution (10\\u202fmg/mL in isopropanol) for 6\\u202fmin. After the perovskite film formation, all the samples were heated at 100\\u202f\\u00b0C in a glove box for different times for experimental purpose.\\n\\nThe ETLs fabricated onto FTO (TEC 8) were used to fabricate the perovskite solar cells. As previously reported, the perovskite layer was processed via a PbI2-xClx seed layer. PbI2 (99.999%, Alfa Aesar) and PbCl2 (99.999%, Alfa Aesar) were dissolved in N,N -dimethylformamide (DMF) and stirred at 60\\u202f\\u00b0C. The molar ratio of the precursor solution (PbI2:PbCl2) was 1:0.5 (1\\u202fM). The PbI2 and PbCl2 mixture was spin-coated at 5000\\u202frpm for 30\\u202fs in a glove box, followed by drying on a hotplate at 70\\u202f\\u00b0C. For the perovskite material conversion, 120\\u202f\\u00b5L of MAI solution (40\\u202fmg/mL) was loaded at 0\\u202frpm for 35\\u202fs, spin-coated at 3500\\u202frpm for 20\\u202fs, and isothermally annealed at 105\\u202f\\u00b0C for 75\\u202fmin under ambient conditions. The films were transferred into the glove box in a N2 atmosphere after annealing. The hole transporting material (HTM) was then spin-coated on the MAPbI3-xClx/ETL/FTO film at 4000\\u202frpm for 30\\u202fs. Poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (MS solutions) (PTAA) solution (20\\u202fmg/mL in toluene) was used as the HTM, including 15\\u202f\\u00b5L Li-TFSI (Li-bis(trifluoro-2-methanesulfonyl)imide)/acetonitrile (170\\u202fmg/mL) and 15\\u202f\\u00b5L tBP (tert-butylpyridine). Finally, Au (70\\u202fnm) was deposited via thermal evaporation.\\n\\nThe absorption spectrum of each sample was obtained using a Cary 5000 (Agilent) instrument. The crystalline structure of the samples was characterized by X-ray diffraction (XRD, Rigaku, dmax 2500\\u202fV, Cu K\\u03b1). The sample morphologies were observed by a field-emission scanning electron microscope (FE-SEM, FEI Quanta 250 FEG). Fourier transform infrared spectroscopy (FTIR, JASCO) analysis was performed by preparing a KBr pellet with the ZnO particles (100:1\\u202fwt) scraped from the corresponding films. Thermogravimetry analysis was conducted using Q600 (TA instruments) at a heating rate of 5\\u202f\\u00b0C/min under a constant N2 flow (100\\u202fmL/min). The J\\u2013V curves of the perovskite solar cells were obtained using an electrochemical station (VSP 200, Bio-Logic) under 100\\u202fmW/cm2 AM 1.5\\u202fG light (Sun 3000 class AAA, ABET Technology) with a metal mask of area (active area) 0.098 and 1\\u202fcm2. The external quantum efficiency (EQE) was measured by a combination of an IVIUM potentiostat (IVIUM) and a monochromator (DONGWOO OPTRON co., Ltd.,) under illumination by an ABET 150\\u202fW Xenon lamp (ABET Technology). Electrochemical impedance spectroscopy was performed with the IVIUM. The obtained Nyquist plots were fitted using Zview software. EQE data acquisition was performed in DC mode.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO-c | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 105.0,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> 75.0,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.098,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"2,2\\u2032,7,7\\u2032-Tetrakis-(N,N-di-p-methoxyphenylamine)-9,9\\u2032-spirobifluorene (spiro-MeOTAD), Methylamine iodide (MAI), lead (II) chloride (PbCl2), and 4-tert-butylpyridine, Lithium bis(trifluoromethanesulfonyl) imide (Li-TFSI), titanium tetraisopropoxide (Ti(OC3H7)4) with the purity of 99.9% were purchased from Xi'an Polymer Light Technology Co. and Sigma-Aldrich respectively, as used without further purification. Fluorine-doped tin oxide (FTO) coated glass was used as the device substrate, purchased from Pilkington with a surface resistance of 7 \\u03a9/sq. MAI and PbCl2 were mixed in anhydrous N,N\\u2032-dimethylformamide (DMF) with a molar ratio of 3:1 for MAI to PbCl2. The MAI-PbCl2 solution was stored in the glovebox under dry nitrogen atmosphere before spin-coating. Spiro-MeOTAD solution was prepared with 72.3 mg spiro-MeOTAD dissolved in 1 mL chlorobenzene, with 28.8 \\u03bcL 4-tert-butylpyridine and 17.5 \\u03bcL Li-TFSI solution (520 mg Li-TFSI in 1 mL acetonitrile) as additives. 0.01 mol Ti(OC3H7)4 was dissolved in 0.80 mL ethanol and acidified by 0.05 mol HCl at a concentration of 0.5 mol/L in deionized water.\\n\\nFTO glass was cleaned in solvent bath of detergent, acetone, isopropanol and deionized water ultrasonically. Surface treatment of oxygen plasma was also performed on the FTO glass to completely remove the organic residues before the spin-coating process. Two methods were applied to prepare the TiO2 layer for comparison. As for the control device, Ti(OC3H7)4 solution was spin-coated on top the clean FTO glass at 2000 rpm and annealed at a typical temperature of 500 \\u00b0C for 40 min. As for the vapor-induced process, FTO substrate spin-coated with Ti(OC3H7)4 was sealed in Teflon-lined stainless autoclave with exposure to water vapor referred to [20]. The substrates were annealed at 180 \\u00b0C for 12 h. The precursor of MAI-PbCl2 was spin-coated onto TiO2 layer in a nitrogen filled glovebox, followed by the annealing at 100 \\u00b0C for 90 min referred to [21]. After the spin-coating of spiro-MeOTAD on top of MAPbI3 layer, the substrate was oxidized overnight in air. Finally, the anode of 100-nm Au was thermal evaporated in high vacuum chamber below 4 \\u00d7 10\\u2212 4 Pa to complete the fabrication process of devices, with the devices area of 0.15 cm2 defined by the overlap area between ITO and Au electrodes.\\n\\nPhotovoltaic measurement employed on a solar cell testing system consisting of a computer-programmed sourcemeter (Keithley 2400) and a solar simulator (AM 1.5, Newport) with a light density of 100 mW/cm2 calibrated by a standard Si photodide.\\nThe thickness of the organic layers was measured using a calibrated surface profiler (Alfa Step-500, Tencor). X-ray diffraction (XRD) patterns were collected on a X-ray diffractometer (D8 Advance, Bruker Co.) using monochromatic Cu source (\\u03bb\\u03ba\\u03b11(Cu) = 0.15418 nm) at 5.0 KV. Top-view morphology was studied via scanning electron microscope (S-4800, Hitachi). X-ray photoelectron spectroscopy (XPS) was measured on the PHI Versaprobe 5000 Scanning X-ray photoelectron spectrometer with Al as the excitation source of 1486.6 eV. The measurement of ultraviolet photoelectron spectroscopy (UPS) was carried out on the surface analysis system of Kratos Co (AXIS Ultra DLD) using the He I line (21.21 eV).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 90,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The perovskite precursor solution was prepared by mixing PbI2, PbCl2 and CH3NH3I in a mixed solvent of \\u03b3-butyrolactone (GBL):dimethylsulfoxide (DMSO) (7:3) with concentrations of 1.25 M, 0.15 M and 1.3 M respectively. PbI2, PbCl2 and CH3NH3I were purchased from Xi\\u2019an p-OLED Inc. ITO glass substrates were sequentially cleaned using detergent, deionized water, acetone, and ethanol in an ultrasonic bath. PEDOT:PSS (4083 Heraeus) was spin-coated onto the oxygen plasm-treated ITO substrates at 4000 rpm for 40 s and then annealed at 120 \\u00b0C in air for 30 min. The perovskite precursor was then deposited onto the ITO/PEDOT:PSS substrates by spin-coating at 1000 rpm for 15 s and 4000 rpm for 30 s. About 35 s after initiation of the spin-coating process, chlorobenzene (400 \\u03bcL) was poured onto the substrates quickly, followed by annealing the film at different preset temperatures (ranging from 90 \\u00b0C to 130 \\u00b0C) for 10 min. Subsequently, the PCBM (25 mg mL\\u22121 in chlorobenzene) was spin coated onto the perovskite films with a thickness of about 60 nm at 2000 rpm for 45 s. After drying for 0.5 h, a poly(ethyleneimine) (PEI) layer was spin coated on top of the film with thickness of several nanometers at 5000 rpm for 60 s from an isopropanol solution (0.1 wt%). Finally, the aluminum (Al) electrodes were thermally deposited with a film thickness of 100 nm under vacuum of 2 \\u00d7 10\\u22126 Torr to fabricate the perovskite solar cells with the ITO/PEDOT:PSS/CH3NH3PbI3\\u2212xClx/PCBM/PEI/Al architecture.\\n\\nThe J\\u2013V characteristics were measured under illumination of AM 1.5G 100 mW cm\\u22122 using a Keithley 2400 source meter. The magneto-photocurrent signals were recorded by measuring the short-circuit current of the PSCs as a function of the magnetic field under excitation from a CW 405 nm laser. The PL spectra and lifetimes of the perovskite films were measured on an Edinburgh fluorescence spectrometer (FLSP920). The X-ray diffraction data were obtained from the perovskite films deposited on a ITO/PEDOT:PSS substrate using a Philips diffractometer (X\\u2019pert PRO MRD). The top-view SEM images of the perovskite films were measured using a FEI Quanta 3D FEG-FIB system.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PEI,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"SnO2 colloid precursor (Sn(IV) oxide, 15% in H2O colloidal dispersion), anhydrous N,N-dimethylformamide (DMF), anhydrous dimethyl sulfoxide (DMSO), anhydrous isopropyl alcohol (IPA), and chlorobenzene were obtained from Alfa Aesar. Methylammonium iodide, PbI2, and spiro-OMeTAD were purchased from Xi'an Polymer Light Technology Co., Ltd. Glucose, lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI), 4-tert-butylpyridine (TBP), and cetyl trimethyl ammonium bromide (CTAB) were obtained from Aldrich. All commercially available materials were used as received without any further purification.\\n\\nCarbon nanodots were synthesized according to our previously reported procedure. The CND-doped SnO2 solution was prepared by mixing carbon nanodots (CNDs) with SnO2 colloid precursor. The MAPbI3 perovskite precursor solution was prepared by dissolving 1.2 M PbI2 and MAI (1:1 molar ratio) in anhydrous DMF/DMSO (9:1, v/v). The 1.2 M FA0.95MA0.05Pb(I,Br)3 perovskite precursor solution was prepared in mixed solvent (DMF/DMSO = 4:1, v/v). CTAB was dissolved in isopropanol at concentrations of 0.5, 1, 2, and 5 mg mL\\u22121. Spiro-OMeTAD/CB solution (72.3 mg mL\\u22121) was prepared using LiTFSI/ACN solution (17.5 \\u03bcL, 520 mg mL\\u22121) and TBP (28.8 \\u03bcL).\\n\\nITO glass substrates were cleaned with detergent, deionized water, and ethanol for 25 min. The CND-doped SnO2 solution was spin-coated on the ITO substrate at 4000 rpm for 20 s and then annealed at 150 \\u00b0C for 30 min. To prepare the MAPbI3 film, precursor solution (80 \\u03bcL) was coated on the SnO2:CNDs substrate at 3000 rpm for 30 s. CB (100 \\u03bcL) was then rapidly dropped onto the substrate 20 s before spin coating was ended. The film was annealed at 100 \\u00b0C for 10 min. To prepare the FA0.95MA0.05Pb(I,Br)3 film, the precursor solution was formed using a two-step process, at 1000 rpm for 5 s and 5000 rpm for 30 s, followed by rapidly dropping CB (100 \\u03bcL) 20 s before the end of the second spin coating step. The obtained film was annealed at 105 \\u00b0C for 20 min. The perovskite film was further treated with CTAB/IPA solution and annealed at 100 \\u00b0C for 10 min. The spiro-OMeTAD layer was formed at 4000 rpm for 30 s. Finally, thermal evaporation was used to form the 80 nm gold back contact.\\n\\nSEM images and energy dispersive spectrometry were obtained using a ZEISS SUPRA55 microscope. TEM images and EDS were obtained using a JEM 1200EX microscope. XRD was conducted using Cu-K\\u03b1 radiation (\\u03bb = 0.15405 nm) at 40 kV and 150 mA. UPS spectra were analyzed using an AC-2 gas detector (Riken Keiki, Japan). The photovoltaic performance was tested using a Keithley 2400 source meter under AM 1.5G illumination with a solar light simulator. Electrochemistry measurements were conducted using a CHI660d electrochemistry station. UV-vis spectrophotometry was performed using a Lambda 950 spectrophotometer. EQE measurements were obtained using a DK240 monochromator from 350 to 800 nm. PL and TRPL spectra were measured using a FLS 980 E fluorometer with excitation at 532 nm. The active cell area was 0.1 cm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: Carbon-np; SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: CTAB | Spiro-MeOTAD,\\n HTL_additives_compounds: Unknown | Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All starting reagents of PbO, CH3NH2, n-C4H9NH2, H3PO2 solution, 2-propanol, DMF, chlorobenzene and HI solution were of analytical grade from Sino-pharm Co. Ltd. and without further purification.\\n\\nThe syntheses of MAI, n-C4H9NH3I and crystal growth were performed according to previously reported methods. But the synthesis of n-C4H9NH3I was based on the reaction of n-C4H9NH2 and HI in an ice bath in an ambient atmosphere. The white BAI in Fig. S2a\\u2020 was obtained using a rotary evaporator and then dried at 60 \\u00b0C at 24 h in air. The newly synthesized BAI (12.060 g, 0.06 mol) and PbO (6.696 g, 0.03 mol) were dissolved in a 200 ml HI and 50 ml H3PO2 mixed solution at 75 \\u00b0C under constant stirring, forming a yellow transparent solution. Solutions were saturated at 60 \\u00b0C. Orange layered BA2PbI4 single crystals have been grown by the top-seeded solution growth (TSSG) method in an ambient atmosphere for about two weeks, as shown in Fig. S1.\\u2020\\nThe newly synthesized BAI (12.060 g, 0.06 mol), MAI (11.925 g, 0.075 mol) and PbO (20.088 g, 0.09 mol) were dissolved in 250 ml HI solution at 65 \\u00b0C under constant stirring, forming a yellow transparent solution. Solutions were saturated at 60 \\u00b0C. Dark red plate and block BA2MA2Pb3I10 single crystals have been grown via different seed direction by the top-seeded solution growth (TSSG) method in an ambient atmosphere for about two weeks, as shown in Fig. 1(a and b).\\nThe newly synthesized BAI (12.060 g, 0.06 mol), MAI (16.700 g, 0.105 mol) and PbO (26.784 g, 0.12 mol) were dissolved in 300 ml HI solution at 65 \\u00b0C under constant stirring, forming a yellow transparent solution. Solutions were saturated at 55 \\u00b0C. Black plate and block BA2MA3Pb4I13 single crystals have been grown with the different seed direction by the top-seeded solution growth (TSSG) method in an ambient atmosphere for about two weeks, as shown in Fig. 1(c and d).\\n\\nFTO glasses were cleaned using an ultra-sonication bath in soap water and rinsed progressively with distilled water and isopropyl alcohol, and finally treated with oxygen plasma for 1 min. A thin blocking-TiO2 layer is first deposited onto fluorine doped tin oxide (FTO) by spin coating titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol) diluted in ethanol (1:15, volume ratio) and annealed at 500 \\u00b0C for 30 min, followed by cooling to room temperature naturally. The mesoporous TiO2 layer composed of 20 nm-sized particles was deposited by spinning coating TiO2 paste (Dyesol 18NRT, Dyesol) diluted in ethanol (1:3.5 wt) at 1500 rpm. After drying at 125 \\u00b0C, the TiO2 films were heated to 500 \\u00b0C, baked at this temperature for 30 min and cooled to room temperature. Before use, the substrates were preheated to 130 \\u00b0C.\\nThe layered perovskite BA2MAn\\u22121PbnI3n+1 (n = 3 and 4) precursor solution was prepared by dissolving 0.24 M perovskite single crystals in DMF. To get the perovskite film, the preheated FTO/TiO2 substrates were immediately transferred to the spin-coated pallet (which is at room temperature), and 60 \\u03bcl of precursor solution was dropped onto the hot substrate. The spin-coater was immediately started with a spinning speed of 3500 rpm for 20 s. Chlorobenzene (200 \\u03bcl) was dropped onto the spinning substrate at 10 s before the end of the procedure. After the spin-coater stopped, the substrates were quickly removed from it. The substrate was dried on a hot plate at 130 \\u00b0C for 10 min.\\nThen the hole transporting material (HTM) was deposited by spin coating the solution of the HTM at 3000 rpm for 60 s. The HTM formulation was prepared by dissolving 2,2\\u2032,7,7\\u2032-tetrakis(N,N-p-dimethoxy-phenylamino)-9,9\\u2032-spirobifluorene (spiro-OMeTAD, 73 mg, Youxuan Tech Co. Ltd.), 4-tert-butylpyridine (tBP, 29.5 \\u03bcl) and a stock solution of lithium bis(trifluoromethylsulphonyl)imide (Li-TFSI, 520 mg ml\\u22121) in acetonitrile (18.5 \\u03bcl) in 1 ml chlorobenzene. Finally, 80 nm gold electrodes were deposited on top of the devices by evaporation at \\u223c10\\u22124 Pa.\\nThe J\\u2013V characteristics were obtained using an Agilent B2900 Series precision source/measure unit, and the cell was illuminated with a solar simulator (Solar IV-150A, Zolix) under AM 1.5 irradiation (100 mW cm\\u22122). The light intensity was calibrated with a Newport calibrated KG5-filtered Si reference cell. The masked active area was 0.1 cm2. J\\u2013V characteristics were obtained using curves recorded from 0.1 V to 1.2 V in the forward and reverse directions with a scanning velocity of 200 mV s\\u22121. For stability measurements, the voltage was fixed at the maximum power point to test the current output for all the test time. The masked active area was 0.1 cm2.\\n\\nSingle-crystal and powder X-ray diffraction, film X-ray diffraction, TGA/DSC, SEM, PL spectra, and UV-vis spectra measurements and fabrication of FASnI3 solar cells are described in detail in the ESI.\\u2020\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: BA2MA2Pb3I10,\\n Perovskite_composition_short_form: BAMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 130,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"MAI was synthesized by reacting hydroiodic acid (50 mL, 57% in water, Sigma-Aldrich) and methylamine (50 mL, 40% in methanol, Junsei Chemical Co. Ltd) in a 250 mL round-bottom flask at 0 \\u00b0C for 2 h with stirring. The precipitate was recovered by evaporation of solvents at 50 \\u00b0C for 1 h with a rotary evaporator. To purify MAI, the products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at room temperature in a vacuum oven for 24 h. MAPbI3 solution (40 wt%) was prepared by mixing the MAI powder and PbI2 (1:1 mole ratio, Sigma-Aldrich) in N,N-dimethylformamide (DMF) at 60 \\u00b0C for 30 min and hydriodic acid was added to the MAPbI3 perovskite solution.\\n\\nFor inverted MAPbI3 planar hybrid solar cells, filtered poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS, Clevios, Al4083)/methanol (1:2 v:v) was coated on a clean ITO glass substrate by spin-coating at 3000 rpm for 60 s and dried at 150 \\u00b0C for 20 min. A 40 wt% MAPbI3/DMF solution containing hydriodic acid (100 \\u03bcL per 1 mL MAPbI3/DMF solution) was then spin coated on the PEDOT:PSS/ITO substrate at 3000 rpm for 200 s and was dried on a hot plate at 100 \\u00b0C for 2 min. A PCBM (nano-C) layer was deposited on the MAPbI3/PEDOT:PSS/ITO substrate by spin-coating PCBM/toluene (20 mg per 1 mL) solution at 2000 rpm for 60 s. Finally, an Au counter electrode was deposited by thermal evaporation.\\nFor normal MAPbI3 planar hybrid solar cells, a 50 nm-thick dense TiO2 electron conductor was deposited on a clean FTO (TEC8, Pilkington) glass substrate by spray pyrolysis deposition with 20 mM of titanium diisopropoxide bis(acetylacetonate) (Sigma-Aldrich) solution at 450 \\u00b0C. The same 40 wt% MAPbI3/DMF with hydriodic acid solution was spin-coated on the TiO2/FTO substrate at 3000 rpm for 200 s and was dried on a hot plate at 100 \\u00b0C for 2 min. A poly(triaryl amine) (PTAA, EM index) hole conductor was deposited on the MAPbI3/TiO2/FTO substrate by spin coating PTAA/toluene (15 mg mL\\u22121) solution containing Li-bis(trifluoromethanesulfonyl)imide (Li\\u2013TFSI)/acetonitrile (7.5 \\u03bcL, 170 mg mL\\u22121) and tBP/acetonitrile (7.5 \\u03bcL, 1:1) additives at 2000 rpm for 30 s. Finally, the Au counter electrode was deposited by thermal evaporation. The active area was fixed as 0.16 cm2. All device fabrication was conducted below relative humidity of 50%.\\n\\nThe current density\\u2013voltage (J\\u2013V) curves were measured by a solar simulator (Peccell, PEC-L01) with a potentiostat (IVIUM, IviumStat) under illumination of 1 sun (100 mW cm\\u22122 AM 1.5G) which is calibrated with a Si-reference cell certificated by JIS (Japanese Industrial Standards). For the measurement of J\\u2013V hysteresis with respect to the scan rate and direction, the forward and reverse scan rate was set to 100\\u20131000 ms per 10 mV. The J\\u2013V curves of all devices were measured by masking the active area with a metal mask of 0.096 cm2. The external quantum efficiency (EQE) was measured by using a power source (150W Xenon lamp, 13014, ABET) with a monochromator (MonoRa-500i, Dongwoo Optron Co., Ltd) and a potentiostat (IviumStat, IVIUM).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: HI,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 4,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: TRUE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless specified otherwise, all chemicals were purchased from Sigma Aldrich or Acros Organics and used as received without purification, Spiro-OMeTAD was purchased from Toronto Research Chemicals Inc., and methylammonium iodide (CH3NH3I) was synthesized according to a previously reported method.\\n\\nThe fluorine-doped tin oxide coated conducting glass substrates (FTO, 15 \\u03a9 per square, NSG, Japan), which were initially etched with 2 M HCl and Zn powder to a certain pattern, were sequentially cleaned in an ultrasonic bath with detergent, distilled water, acetone, isopropanol and then dried with a nitrogen stream and treated in oxygen plasma for 10 min.\\nThe devices with FTO/C-TiO2/M-TiO2/MAPbI3/spiro-OMeTAD/Au were prepared according to the following process. A TiO2 compact layer (C-TiO2), which can reduce the recombination of the electrons and holes in FTO, was prepared by spin-coating (3000 rpm, 45 s) a mildly acidic solution of titanium isopropoxide in isopropanol on the as-cleaned FTO substrates according to the reported procedure and then annealing at 500 \\u00b0C for 30 min. Before using, the as-prepared C-TiO2 substrates were immersed in a 0.02 mM TiCl4 solution at 70 \\u00b0C for 30 min and sintered at 500 \\u00b0C for 30 min after rinsing with deionized water and ethanol. After cooling to room temperature, the TiO2 mesoporous layer (M-TiO2) was deposited on the as-prepared C-TiO2 by spin-coating (5000 rpm, 45 s) commercial TiO2 paste (Dyesol 18NR-T) that was diluted with anhydrous ethanol at a weight ratio of 2:7 and heated at 150 \\u00b0C for 20 min on a hot plate and then the substrates coated with M-TiO2 were subsequently sintered at 500 \\u00b0C for 30 min in an annealing furnace in air.\\nThe CH3NH3PbI3 films were formed using two-step sequential deposition procedure (TSSSD) in a glovebox with N2 atmosphere. A 462 mg mL\\u22121 (1 M) PbI2 solution was obtained by dissolving PbI2 into anhydrous DMF with continuous stirring and heating at 70 \\u00b0C for 12 h in the dark. The CH3NH3I solution was prepared by dissolving 8 mg CH3NH3I in 1 mL isopropanol with stirring at room temperature. For the perovskite layer preparation, the PbI2 layer was first deposited by spin-coating a hot PbI2 solution on the FTO/C-TiO2/M-TiO2 substrates at 3000 rpm for 5 s and 5000 rpm for 5 s. For superior reproducibility of the devices, it is significant to continue heating the PbI2 solution at 70 \\u00b0C in this process. After depositing the PbI2 layer, 70 \\u03bcL CH3NH3I solution in isopropanol was dropped onto the as-prepared PbI2 layer for 20 s, which was spun with a speed of 6000 rpm for 20 s. After washing with clean anhydrous isopropanol, the films were annealed with two different heating process (TA and ITA) at 80 \\u00b0C, 100 \\u00b0C, 130 \\u00b0C, and 160 \\u00b0C for 20 min onto a hot plate. Once the films completely converted into the CH3NH3PbI3, 20 \\u03bcL of HTM solution was dropped onto the CH3NH3PbI3 perovskite layer and spin-coated at 4000 rpm for 30 s. The HTM solution was prepared by dissolving 72.3 mg 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (spiro-MeOTAD) in 1 mL anhydrous chlorobenzene, and 30 \\u03bcL 4-tert-butylpyridine (tbp) and 18 \\u03bcL of lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg Li-TSFI in 1 mL acetonitrile) was then added as an additive with stirring. The devices were then left in a dry air atmosphere with a low relative humidity in the dark for spiro-MeOTAD oxidation. Finally, 80 nm of the back contact electrodes were deposited via thermally evaporating Au on the top of the spiro-MeOTAD coated devices under a pressure of ca. 10\\u22126 Torr.\\n\\nScanning electron microscopy (SEM) images were recorded by Rili SU 8000HSD Series Hitachi New Generation Cold Field Emission SEM. Atomic force microscopy (AFM) analysis of the perovskite films without depositing HTM and Au were performed using a Bruker Dimension ICON-PT with Co/Cr tips. X-ray diffraction patterns of the perovskite films were obtained using a Shimadzu XRD-6000 X-ray Diffraction instrument with Cu-K\\u03b1 radiation. The UV-Vis absorption measurements were carried out on a Japan Shimadzu model UV-2250 spectrophotometer. A steady-state (Ss) and time-resolved (Tr) FLS 920 luminescence spectrometer with an excitation wavelength of 425 nm that passed through a 650 nm low-pass filter. The annealing temperature and time of all samples was 100 \\u00b0C and 20 min, respectively. In particular, the samples for XRD and PL characterizing were produced by directly spin-coating the precursor solution on clean glass slides using the TSSSD procedure.\\nThe photocurrent and voltage properties of PSCs were characterized using CHI660D electrochemical workstation by applying an external bias potential to the solar cells under simulated AM 1.5G sunlight (100 mW cm\\u22122) generated from an AAA Class 150 W solar simulator (SAN-EI ELECTRIC, model XES-40S2-CE, Japan) with an AM 1.5G type filter. The light intensity was calibrated by a Newport Oriel PV standard reference cell and meter (model 91150 V); the photoactive area of the solar cells was 0.09 cm2, as determined by an metal aperture and the scan rate was 20 mV s\\u22121. Electrochemical impedance spectra (EIS) were obtained on a CHI660D electrochemical workstation (Chenhua, China) at a frequency ranging from 0.1 to 105 Hz with 5 mV perturbation. The impedance spectra data was fitted using the Z-SimpWin software. The External Quantum Efficiency (EQE) were recorded by IPCE measurement system (model 2931-C, Newport, USA) using a 300 W xenon lamp (model 66902, Newport, USA) with a 1/4 monochromator (model 74125 Oriel Cornerstone 260, Newport, USA), light intensity was calibrated using a silicon detector (model 71675, Newport, USA).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> Unknown,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> 20.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals and solvents were purchased from Aldrich and used as supplied. NMR spectra were recorded on a Bruker AC400 instrument operating at 400 MHz for 1H and 101 MHz for 13C. Chemical shifts for 1H and 13C (\\u03b4) are given in ppm relative to (CH3)4Si. High resolution mass spectrometry data was obtained using recorded using positive electrospray at the EPSRC National Mass Spectrometry Service at the University of Swansea.\\nCyclic voltammetry was recorded on HTMs (0.1 mM (3) and 0.1 mM (5)) at 25 \\u00b0C in N2-saturated anhydrous CH2Cl2 using 0.1 M Bu4NPF6 as the supporting electrolyte. Measurements were performed using a CHI 440a electrochemical analyzer with a sweep rate 0.1 V s\\u22121 using a three-electrode cell with a Pt (12.5 mm2) working electrode, a Ag wire pseudo-reference electrode and a Pt wire counter electrode. Potentials are reported vs. Fc/Fc+ (E1/2 = 0.308 V vs. Ag wire) and are adjusted to 0 V. The corresponding electron affinities and ionization potentials are calculated relative to the Fc/Fc+ redox couple (\\u20134.8 eV) using squarewave voltammetry.\\nTG-BC TFTs were fabricated on glass substrates. The substrates were cleaned with acetone and isopropanol (IPA) in a sonication bath for 10 min for each step. 40 nm thick Au source and drain electrodes (channel width/length: 1000 \\u03bcm/30 \\u03bcm) were evaporated through shadow masks under vacuum, before being treated with a work function modifier pentafluorothiophenol (PFBT) self-assembled monolayer (SAM). For the SAM treatment, the substrates were submerged in a 5 mmol L\\u22121 PFBT in IPA solution for 60 min. Upon completion of the SAM treatment, the substrates were rinsed with large amount of IPA to remove excessive unbonded PFBT and then blow-dried with N2. The HTMs were deposited from a solution via spin coating at 2000 rpm for 30 s in a N2 atmosphere. Following semiconductor depositions, a Teflon based material (AF2400, Dupont) dissolved in a Fluorinert\\u2122 electronic liquid (FC-43, 3 M) at a concentration of 25 mg ml\\u22121 and used as the gate dielectric was deposited via spin cast (1000 rpm, 30 s) to produce a \\u223c330 nm thick dielectric layer, which was then annealed for 10 min at 40 \\u00b0C in N2. The TFTs were completed by thermal evaporation of 50 nm thick Al gate electrodes through shadow masks under high vacuum.\\nLinear field-effect mobility was calculated using gradual-channel approximation:\\nTrap density was evaluated from the following equation:\\n\\nElectron-transporting layer. 0.05 M SnCl4\\u00b75H2O (Sigma) was first dissolved in anhydrous IPA (Sigma) and stirred for 30 min at room temperature. The solution was deposited on cleaned FTO substrates with 3000 rpm spin rate for 30 s, followed by pre-drying at 100 \\u00b0C for 10 min and then heat-treated at 180 \\u00b0C for 1 h. The films were then treated using chemical bath deposition method, as described elsewhere. 500 mg urea was dissolved in 40 ml deionized water, followed by the addition of 10 \\u03bcl mercaptoacetic acid (Sigma) and 0.5 ml HCl (VWR; 37 wt%). Finally, SnCl2\\u00b72H2O (Sigma) was dissolved in the solution at 0.002 M and stirred for 2 min. The deposition was made by putting the substrates vertically in a glass container filled with the above solution, in a 70 \\u00b0C oven for 3 h. The treated substrates were rinsed in a sonication bath of deionized water for 2 min, dried in a stream of N2 and annealed for 1 h at 180 \\u00b0C.\\nPerovskite absorber layer. FA0.83Cs0.17Pb(I0.9Br0.1)3 perovskite precursor solution were dissolved in a 4:1 (v:v) mixture of anhydrous DMF:DMSO (Sigma) to obtain a stoichiometric solution with desired composition using precursor salts: formamidinium iodide (FAI; Dyesol), caesium iodide (CsI; Alfa Aesar), lead iodide (PbI2; TCI), lead bromide (PbBr2; TCI). The concentration was 1.4 M. The solution was made in a N2-filled glovebox and kept stirring overnight at room temperature. The perovskite precursor solution was deposited through a two-step spin coating program (10 s at 1000 rpm and 32 s at 6000 rpm) with dripping of chlorobenzene (Sigma) as anti-solvent during the second step, 8 s before the end. All the films annealed at 100 \\u00b0C for 60 min.\\nHole-transporting layer. TAT-tBuSty was dissolved in chlorobenzene (35 mM). Spiro-OMeTAD (Borun Technology 99.8%) was dissolved in in chlorobenzene (70 mM). 10.7 mol% of tert-butylpyridine (Sigma; tBP) and 25 mol% tris(bis(trifluoromethylsulfon-yl)imide) (Sigma; Li-TFSI) (from a 1.8 M stock solution in acetonitrile) were added as additives. The final HTM solutions were spin-coated onto the perovskite layers at 2000 rpm for 45 s.\\nElectrode deposition. 80 nm gold electrodes were thermally evaporated under vacuum of \\u223c5 \\u00d7 10\\u22126 Torr, at a rate of \\u223c 1 \\u00c5 s\\u22121. Note that the temperature of the vacuum chamber was controlled (<40 \\u00b0C) during the evaporation of the metal electrodes as higher temperature will cause possible degradation of perovskite films.\\n\\nThe current density\\u2013voltage (J\\u2013V) curves were measured (2400 Series SourceMeter, Keithley Instruments) under simulated AM 1.5G sunlight at 100 mW cm\\u22122 irradiance generated by an Abet Class AAB sun 2000 simulator, with the intensity calibrated with an NREL calibrated KG5 filtered Si reference cell. The mismatch factor was calculated to be less than 5%. The active area of the solar cell is 0.0919 cm\\u22122. The forward J\\u2013V scans were measured from forward bias (FB) to short circuit (SC) and the backward scans were from short circuit to forward bias, both at a scan rate of 380 mV s\\u22121. A stabilization time of 5 s at forward bias of 1.4 V under illumination was done prior to scanning.\\n\\nX-ray diffraction measurements were carried out using a Bruker D8 Discover with Da Vinci software with a copper source (40 kV, 40 mA). Tests were carried out using 0.05 2Theta increments with a 0.5 second step time.\\n\\nFluoride-doped SnO2 (FTO) coated glass substrates (Solaronix) were ultrasonicated in acetone followed by O2 plasma cleaning. Chlorobenzene solutions of TAT-tBuSty (35 mM) or spiro-OMeTAD (Borun Technology 99.8%) i (70 mM) were prepared each containing 10.7 mol% of tert-butyl pyridine (Sigma) and 25 mol% tris(bis(trifluoromethylsulfon-yl)imide) (Sigma; Li-TFSI). The HTM solutions were spin-coated onto the glass at 2000 rpm for 45 s. Both of the HTM layers were measured as ca. 90 nm with a DekTak profilometer. To measure HTM film stability, control samples were left in air at ambient temperature. A second set of films were heated to 80 \\u00b0C for 30 min and then allowed to cool to ambient temperature for 30 min; this sequence made once heating cycle. After each cycle, the films were analysed by UV-visible spectrometry (Varian Cary 5000) and digital imaging using a Canon EOS 1100D camera (F-stop 29, exposure time 0.3 s, ISO 100) in a Photosimile 200 lightbox. RGB data were extracted and analysed as described by Furnell et al.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: CBD,\\n Perovskite_composition_long_form: Cs0.17FA0.83PbBr0.3I2.7,\\n Perovskite_composition_short_form: CsFAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0919,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2, TCI) was dissolved in DMF:DMSO (9:1) with a concentration of 0.6 g mL\\u22121. The amount of DMSO was adjusted to have a small excess molar amount over PbI2. The solution was then filtered through a 0.2 \\u03bcm PTFE syringe filter to remove any aggregated particles and dust. The PbI2\\u2013DMSO films were formed by spin-casting of the solution at 2000 rpm for 30 s. The films were then immediately dipped in anhydrous 2-propanol (IPA, Sigma-Aldrich) with subsequent blowing with compressed air in order to remove excess IPA from the film. The resulting PbI2 films were dipped into a solution of CH3NH3I (MAI, Greatcell Solar Ltd.) mixed with CH3NH3Cl (MACl, Sigma-Aldrich, 25 wt% with respect to MAI) in IPA to convert them to perovskite. The films were rinsed with IPA twice to remove any excess MAI from the surface. The remaining IPA was removed by air blowing, then the perovskite films were placed on a hot plate at 100 \\u00b0C. For the slot-die coating, a table-top slot-die coater (PMC-200, PEMS, South Korea) was used. A PbI2\\u2013DMSO complex (0.3 g mL\\u22121) was deposited at a rate of 10 mm s\\u22121 with a gap of 100 \\u03bcm. The films were blown by an air-knife equipped with the slot-die coater before it was immersed in the IPA bath. The rest of the procedure was the same as that for spin-coated films.\\n\\nF-doped SnO2 glasses (FTO, Pilkington TEC-15) were cleaned by ultrasonication in detergent, DI-water, and ethanol for 30 min each before use. An SnO2 layer was formed by sequential spin-coating of SnO2 nanoparticles (Alfa Aesar, 20 wt% in water) and SnCl4\\u00b75H2O (Sigma-Aldrich) solutions. First, 2.67% of SnO2 nanoparticles dispersed in water were spin-coated at 2000 rpm for 30 s. The substrates were then annealed at 150 \\u00b0C for 30 min. As the next step, SnCl4\\u00b75H2O in IPA was spin-casted at 2000 rpm for 30 s. The subsequent films were annealed at 180 \\u00b0C for 1 h. The perovskite layers were deposited on the substrate by the aforementioned MET or heat treatment of PbI2\\u2013DMSO. In order to fabricate the perovskite layer by heat treatment, PbI2\\u2013DMSO solution (0.6 g ml\\u22121) was spin-coated and then annealed at 70 \\u00b0C for 30 min. The resulting PbI2 films were immersed in MAI solution under the same conditions as for MET. As a hole-transporting layer, 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene (spiro-OMeTAD, LumTec) was spin-coated at 2000 rpm for 30 s. Spiro-OMeTAD was dissolved in chlorobenzene at a concentration of 90.9 mg ml\\u22121, with 23 \\u03bcL of bis(trifluoromethane)sulfonimide lithium salt (Li-TFSI)/acetonitrile (540 mg ml\\u22121), 39 \\u03bcL of 4-tert-butylpyridine (tBP, Sigma-Aldrich), and 10 \\u03bcL of tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) tri[bis(trifluoromethane)sulfonamide] (FK209, LumTec)/acetonitrile (0.376 g ml\\u22121). Au counter electrodes were deposited by thermal evaporation.\\n\\nThe top-view images of PbI2\\u2013DMSO, PbI2 and MAPbI3 films were obtained by using a field emission scanning electron microscope (SEM, Mira 3 LMU, Tescan) operated at 20 kV. The X-ray diffraction patterns were measured by using a Rigaku SmartLab X-ray diffractometer. GI-WAXS measurements were conducted at the Pohang Accelerator Laboratory (PAL) at beamline 6D. The incident angle for the X-rays (11.6 eV) was 0.34\\u00b0, and the samples were exposed to the X-rays for 60 s. The spectra were analysed using Igor Pro 7.0 software (WaveMetrics) with GISAXSshop (Dr Byeongdu Lee, Argonne National Lab.). The J\\u2013V curves were obtained using a solar simulator (Newport, Oriel Class A, 91195A) with a voltage sourcemeter (Keithley 2400) under 100 mA cm\\u22122 illumination under standard AM1.5G conditions. Light intensity was calibrated with an Si-reference cell certified by the NREL, USA. The samples were all masked with a metal-mask with an active area of 0.096 cm2. The external quantum efficiency (EQE) was measured using a power source (Newport 300 W Xenon lamp, 66920) with a monochromator (Newport Cornerstone 260) and a multimeter (Keithley 2001).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: SnCl4,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: 30.0 >> Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.096,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless stated otherwise, all chemicals were purchased from Sigma-Aldrich and used as received. TiO2 paste, 2,2\\u2032,7,7\\u2032-tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9\\u2032-spirobifluorene (spiro-MeOTAD) (\\u226599.0%), Li-bis(trifluoromethanesulfonyl) imide (Li-TFSI) (\\u226599.5%), and 4-tert-butylpyridine were purchased from Yingkou Optimal Choice Trade CO., Ltd. (China). CH3NH3I (MAI) was synthesized by the procedure stated previously.\\nPrior to fabrication, the fluorine-doped tin oxide (FTO, 7 \\u03a9 sq.\\u22121) substrates were carefully patterned and cleaned, as stated in our previous work. A thin compact TiO2 layer (c-TiO2) was deposited on the patterned FTO by spray pyrolysis at 450 \\u00b0C by using 0.2 M Ti(IV) bis(ethylacetoacetate)-bis(ethyl acetoacetate)-diisopropoxide 1-butanol solution, followed by annealing in air at 450 \\u00b0C for 1 h. The mesoporous TiO2 layer (mp-TiO2) was introduced from a 100 \\u03bcL diluted TiO2 in ethanol by spin coating at 5000 rpm for 30 s. After drying at 125 \\u00b0C for 5 min, the TiO2 films were baked at 500 \\u00b0C for 20 min and then cooled to room temperature. Prior to their use, the films were dried again at 500 \\u00b0C for 30 min. The thickness of the annealed TiO2 film was around 280 nm, as determined by scanning electron microscopy (SEM; Hitachi S-4800). The PbI2 solution was prepared by dissolving 0.698 g of PbI2 (99%, Sigma-Aldrich) in 1.5 mL of DMF at 70 \\u00b0C for 12 h under static conditions. Before use, the solution was filtered through a 0.22 \\u03bcm PTFE syringe filter. The PbI2 solution (30 \\u03bcL) was spin-coated on the mesoporous TiO2 film at 1300 rpm for 5 s and 4000 rpm for 20 s, and the annealing-free, wet PbI2 films were then instantly dropped with a solution of CH3NH3I in 2-propanol (150 \\u03bcL, 20 mg mL\\u22121) and spin-coated at 4000 rpm for 30 s with a loading time of 30 s. Afterward, the as-prepared films were heated at 100 \\u00b0C for 30 min until the colour changed to dark red. A volume of 40 \\u03bcL of spiro-MeOTAD solution was spin-coated on the MAPbI3 perovskite layer at 4000 rpm for 30 s to fabricate the hole transporter layer (HTL) in an Ar-filled glovebox (H2O and O2 < 1 ppm). The spiro-MeOTAD solution was prepared by dissolving 72.3 mg of spiro-MeOTAD in 1 mL of chlorobenzene, to which 17.5 \\u03bcL of lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg mL\\u22121 in anhydrous acetonitrile) and 29.0 \\u03bcL of 4-tert-butyl pyridine were added. After being left overnight in the dry dark box, a 120 nm thick Ag electrode was deposited by thermal evaporation on the spiro-MeOTAD-coated film to complete the fabrication of the cell device. The active area of the devices was determined to be 0.12 cm2 by a shadow mask.\\n\\nUV-vis spectra of the perovskite films on mesoporous TiO2 film were obtained by an UV-vis spectrophotometer (Agilent, model Cary 60). X-ray diffraction (XRD) patterns were measured on a Rigaku D/MAX 2400 diffractometer with Cu K\\u03b1 radiation at a scan rate of 3\\u00b0 min\\u22121 under operation condition of 35 kV and 200 mA. A Hitachi S-4800 field-emission scanning electron microscopy (SEM) operated at 10 kV was used to characterize the morphologies of the samples and the cross section of the devices. The root-mean-square roughness (RMS) of the perovskite films were measured by using an atomic force microscopy (AFM, NanoScope III microscope, Digital Instrument) in tapping mode. The J\\u2013V curves were measured on a Keithley 2400 source meter under AM 1.5G illumination (100 mW cm\\u22122). The NREL-calibrated Si solar cell with KG-2 filter was employed to adjust light intensity into 1 sun illumination. A black aperture mask with the area of 0.09 cm2 was used to prevent scattered light during J\\u2013V measurement. The external quantum efficiency spectra were recorded on a SM-250 Hyper Monolight system. Time-resolved photoluminescence (PL) decay spectra of glass/MAPbI3/PMMA films were measured on a steady-state and time-resolved fluorescence spectrofluorometer (PTI model, QM/TM/IM) with a 579 nm photoluminescence dye for excitation at room temperature, where poly(methyl methacrylate) (PMMA) serves as protective layer for perovskite films. Impedance spectroscopy (IS) was performed on an impedance/gain-phase analyzer (Solartron SI 1260) with a bias voltage of 0.7 V, a modulation amplitude of 10 mV, and a frequency ranging from 100 kHz to 1 Hz under 1 sun illumination.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 30.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The synthesis of all HTMs is depicted in Scheme 1. Condensation of 3,6-dibromofluorenone (1) with 4-methoxy-N-(4-methoxyphenyl)-N-phenylaniline (2) employing Eaton's reagent (7.7% w/w P2O5 in MeSO3H) yields fluorene derivative 3 in moderate yield. Subsequent palladium cross-coupling with the appropriate arylamine provides HTM1 and HTM2. The synthesis of HTM3 is undertaken from 2,6-dibromocyclopenta[2,1-b:3,4-b\\u2032]dithiophen-4-one (6), which was previously obtained following the procedure described by Wang, by Corey\\u2013Fuchs reaction with PPh3 and CBr4 to yield compound 7 in moderate yield. The final step is a fourfold Suzuki reaction to couple triarylamine 5. Detailed synthetic procedures and characterization may be found in the ESI.\\u2020\\n\\nFTO coated glass (NSG10) was sequentially cleaned by sonication in a 2% Hellmanex solution and isopropanol for 15 min, respectively. A 20 nm to 50 nm titania blocking layer was applied on the substrates by spraying a solution of titanium diisopropoxide bis(acetylacetonate) in ethanol at 450 \\u00b0C. For the 200\\u2013300 nm mesoporous TiO2 layer, 30 NR-D titania paste from Dyesol diluted in ethanol (150 mg ml\\u22121) was applied by spin-coating at 4000 rpm for 10 s followed by a sintering step at 500 \\u00b0C for 30 min. The MAPbI3 perovskite precursor solution was prepared by mixing 461 mg PbI2 and 159 mg methylammonium iodide in 800 \\u03bcl of DMSO. The perovskite layers were fabricated by a single step spin-coating procedure reported by Seok et al. The perovskite solution was spun at 1000 rpm for 10 s followed by 5000 rpm for 30 s using a ramp of 3000 rpm s\\u22121. 15 s prior to the end of the spin-coating sequence 100 \\u03bcl of chlorobenzene were poured onto the spinning substrate. Afterwards, the substrates were transferred onto a heating plate and annealed at 100 \\u00b0C for 45 min. Spiro-OMeTAD (2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenyl-amine)9,9\\u2032-spirobifluorene), HTM1, HTM2 and HTM3 were used as hole transporting materials and applied from a solution in chlorobenzene. Optimized concentrations were found to be 70 mM for Spiro-OMeTAD and 30 mM for the new HTMs. tert-Butylpyridine (Tbp), tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) (FK209) and tris(bis(trifluoromethylsulfonyl)imide) (Li-TFSI) were added as additives: 330 mol% Tbp, 50 mol% Li-TFSI from a 1.8 M stock solution in acetonitrile and 3 mol% FK209 from a 0.25 M stock solution in acetonitrile. The HTM solution was spin-coated dynamically onto the perovskite layers at 4000 rpm for 20 s. The gold electrodes were deposited by thermal evaporation of 80 nm gold using a shadow mask under high vacuum conditions.\\n\\nThe photovoltaic device performance was analysed using a VeraSol LED solar simulator (Newport) producing one sun AM 1.5 (100 mW cm\\u22122) sunlight. Current\\u2013voltage curves were measured in air with a potentiostat (Keithley). The light intensity was calibrated with an NREL certified KG5 filtered Si reference diode. The solar cells were masked with a metal aperture of 0.16 cm2 to define the active area. The current\\u2013voltage curves were recorded scanning at 20 mV s\\u22121.\\n\\nThe device is connected to a high impedance (1 M\\u03a9) input channel of an Oscilloscope to provide the open-circuit condition. A white LED is used to illuminate the device continuously in the background (BGL) to generate steady-state charge carrier density creating VOC. A weak 532 nm pulsed laser is applied on top of the BGL to create a small number of additional charge carriers (causing an increase in open-circuit voltage, \\u0394VOC), which decays in time after the light pulse switches off. The rate of the green laser pulse is set to 6 Hz. TPC is the same as TPV, and the only difference is that the device is connected to the oscilloscope's 50 \\u03a9 input channel instead of 1 M\\u03a9. Both BGL and pulsed light intensities are controlled by neutral density filters. TPV/TPC signals are recorded with a Picoscope 6424 controlled by a custom-built Python program. The simulation of the TPC/TPV is done by GPVDM software developed by R. C. I. MacKenzie, which models the device parameters by solving the drift-diffusion, carrier continuity, and Poisson's equations. First, the parameters of the model are optimized to reproduce the J\\u2013V characteristics of our reference devices with Spiro-OMeTAD. Then, the TPV/TPC are modeled using the same parameters, and only the targeted parameter is allowed to vary when a certain parameter is needed to be swept for a range. The parameters and related results can be found in the ESI.\\u2020\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methyl ammonium iodide (CH3NH3I) was synthesized via the reaction of methylamine (CH3NH2, 21.6 mL, 40 mass% in water, Alfa Aesar) and hydroiodic acid (HI, 30 mL, 57 mass% in water, with hypophosphorous acid H3PO2 1.5%, Alfa Aesar) and stirred at 0 \\u00b0C for 2 h under a N2 atmosphere, followed by rotary evaporation to remove the solvent. The CH3NH3I powder was washed three times with diethyl ether (99%, anhydrous, ECHO) and dried in a vacuum oven at 50 \\u00b0C overnight before use. CH3NH3I was synthesized as described elsewhere. MAPbI3 precursor solutions (concentration 45% by mass) were prepared in N,N-dimethyl formamide (DMF, anhydrous, Aldrich, 1 mL) mixed with powdered CH3NH3I (175 mg) and PbI2 (99%, Aldrich, 507 mg). The solution was stirred at 70 \\u00b0C for 1 h before use.\\n\\nBefore ALD, FTO (TEC7, Hartford, USA) was partially removed from the substrate via etching with zinc powder and HCl (2 M) to produce the desired pattern. The patterned FTO substrates were cleaned with ultrasonication for 30 min in a mixture (acetone, soapy water and isopropyl alcohol (IPA), 1:1:1) and then washed with deionized water. Afterwards, the glass was dried with a N2 blower. Dense thin films of titanium dioxide as HBL with varied thickness were deposited onto the FTO substrate using a commercial hot-wall flow-type ALD reactor (SUNALETM R series, Picosun, Finland). The deposition involved alternating exposure of TiCl4 and deionized water vapor at process temperature 300 \\u00b0C with a precursor carrier and purge gas N2 at pressure 1.6 kPa. The pulse and purge times for the precursors were 0.1 and 4 s, respectively. The rate of deposition of TiO2 on the FTO glass was estimated to be 0.43 \\u00c5 per cycle. To fabricate uniform, one-side deposited TiO2 films, we attached the FTO glass tightly to a smooth cover glass, which was previously washed with deionized water in an ultrasonic bath for 5 min. After that, a m-TiO2 layer of thickness approximately 200 nm was spin-coated (100 \\u03bcL, 3000 rpm, 30 s) and annealed at 450 \\u00b0C for 30 min. The substrates were subsequently exposed to ozone for 18 min via irradiation (excimer lamp PC-01-H, N-Cobo Co.) under an O2 atmosphere to remove the organic residues. The prepared MAPbI3 precursor solution was deposited onto the prepared substrate with spin coating at 5000 rpm for 15 s; a few drops of chlorobenzene (CBZ) as an anti-solvent were dripped onto the substrate during spin coating after a delay (5 s). The MAPbI3-precursor coated substrates were then dried on a hot plate at 100 \\u00b0C for 10 min. The HTM layer with a solution containing spiro-OMeTAD (125 mg, Lumtec), Li-TFSI (7.8 mg, Aldrich) in acetonitrile (15.6 \\u03bcL) and 4-tert-butylpyridine (TBP, 22.6 \\u03bcL) dissolved in chlorobenzene (1 mL) was then deposited via spin coating at 2000 rpm for 30 s. The sample was transferred to a vacuum system (10\\u22126 Torr) in which silver (thickness \\u223c 150 nm) was evaporated through a shadow mask to complete the device fabrication; the active area of the Ag electrodes in the fabricated device was 0.09 cm2.\\n\\nStructure and surface measurements. The crystalline phases were identified with XRD (RINT-2000/PC RIGAKU, Cu K\\u03b1 radiation, scanning speed 2\\u00b0 (2\\u03b8)/min within 2\\u03b8 range 5\\u201360\\u00b0). The particle morphology and structure were examined with a FESEM (Hitachi SU8010, maximum resolution 1 nm at electron acceleration voltage 15 kV) and an AFM (nanoscale hybrid microscope VN-8010, Keyence microscope, Japan). To analyze the chemical composition of the surfaces we used an X-ray photoemission spectrometer (JPS-9200, JEOL) to record the X-ray photoemission spectrum. The Al K\\u03b1 line served as the X-ray source; the C 1s signal served as an internal reference (284.6 eV).\\nPhotovoltaic and PL lifetime measurements. The J\\u2013V curves were measured with a digital source meter (Keithley 2400) under one-sun illumination (AM 1.5 G, 100 mW cm\\u22122) from a solar simulator (XES-40S1, SAN-E1). The IPCE spectra were recorded with a system comprising a Xe lamp (A-1010, PTi, 150 W) and monochromator (PTi, 1200 groove mm\\u22121 blazed at 500 nm). PL transients were recorded with a TCSPC system (Fluotime200, PicoQuant) with excitation at 635 nm from a picosecond pulsed-diode laser (LDH-635, PicoQuant, FWHM \\u223c 70 ps); the PL temporal profiles were recorded at 770 nm.\\nConductivity measurements. We used an electrochemical analyzer (ALS/CH Instruments 852C, ALS) with a copper lead wire. The experimental setup of the measurements is as follows: two electrodes of the electrochemical analyzer were connected to the samples, one to the FTO part and the other to the compact ALD-TiO2 surface. We measured the resistivity at various positions on the compact ALD-TiO2 surface. Almost 15 positions have been tested for each sample to derive their mean. The distance between the two electrodes was stable for all measurements and for all compact ALD-TiO2 of varied thickness to make the comparison among them more precise.\\nNumerical simulations. The FDTD simulation was performed with the Lumerical FDTD solution software package on a discrete, non-uniformly spaced mesh with a maximum resolution of 2.0 nm. The TiO2 substrate was assumed to behave as a dielectric with a refractive index n = 2.5. In the simulation, a linear polarized plane wave was irradiated onto the structures from TiO2 at a normal incidence angle; the surface roughness of TiO2 at the interface of TiO2 and PSK was varied from 0 to 40 nm as the root-mean-square roughness (Rrms).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: ALD | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Barium iodide (BaI2, 99.9%), (1S)-(+)-10-camphor sulfonic acid (CSA, 99%), cesium iodide (CsI, 99.9%), lead iodide (PbI2, 99.9%), dimethyl sulfoxide (DMSO, anhydrous, 99.8%), poly(3-hexylthiophene-2,5-diyl) (P3HT, with 85000\\u201310000 wt), chlorobenzene (CB, anhydrous 99.8%) and all other chemicals including N,N-dimethylformamide (DMF, anhydrous, 99.8%) were purchased from Sigma-Aldrich. All salts and solvents were used as received without further purification.\\n\\nThe CsPbI3 precursor solution was prepared by dissolving CsI and PbI2 (1:1 mmol) with a mixture of DMSO and DMF (4:6, v/v) as the solvent. The Ba2+-incorporated CsPbI3 perovskite precursor solution was prepared by dissolving 0.01 mol CsI and 0.01 mol (90/10 mol%) mixture of PbI2/BaI2 and CSA (2, 5, and 10 wt% of CsPb1\\u2212xBaxI3) in 1 mL of solvent with a mixture of DMSO and DMF (4:6, v/v). The final solution was stirred for 2 h at room temperature. The HTL solution was prepared by dissolving P3HT (10 mg) in 1 mL chlorobenzene and adding 10 \\u03bcL of (4F-TCNQ-Sigma-Aldrich) in chlorobenzene (1 mg/1 mL).\\n\\nFirstly, indium tin oxide (ITO) conducting glass was ultrasonically cleaned using detergent, deionized water, acetone and isopropyl alcohol for 15 min each and then treated by a UV/O3 cleaner for 30 min. Then, a compact \\u223c20 nm thin SnO2 layer was spin-coated on the glass/ITO substrate followed by annealing at 150 \\u00b0C for 15 min. After depositing the electron transport layer, the perovskite layer was deposited via a one-step spin-coating method using the 1 mM CsPbI3 precursor solution at the speed of 3000 rpm for 30 s followed by annealing at 60 \\u00b0C for 1 min and then at 120 \\u00b0C for 10 min. Then, an HTL layer of P3HT was spin-coated at 3000 rpm for 30 s at a ramp rate of 1000 rpm s\\u22121. Finally, an 80 nm thick gold electrode as the top electrode was deposited through a shadow mask using thermal evaporation with an active area of 0.130 cm2.\\n\\nA digital source meter (Keithley 2635A) was used to measure the current density\\u2013voltage (J\\u2013V) characteristics of the solar cells. The solar cell performance was measured under illumination by an Air Mass 1.5 Global (AM 1.5 G) solar simulator with an irradiation intensity of 100 mW cm\\u22122. Apertures (13.0 mm2) made of thin metal were attached to each cell before the measurement of the J\\u2013V characteristics. The device stability was measured in time step. EQE measurements were obtained with a PV measurement QE system under ambient conditions, with monochromated light from a xenon arc lamp. The monochromatic light intensity was calibrated with an Si photodiode and chopped at 100 Hz. The absorption properties of the thin films were characterized by UV-Vis-NIR spectroscopy (Carry 5000, Agilent), while thin film PL was measured with a fluorometer (Carry Eclipse, Agilent) excited at 450 nm. The surface morphologies of the perovskite with/without additive were analyzed by field emission SEM (Nova NanoSEM, FEI). Fourier transform infrared (FTIR) spectra of the thin films were measured using a 670-IR, Varian spectrometer. Crystallographic information was determined by high power XRD (MAX 2500V, Rigaku) using Cu K\\u03b1 radiation (\\u03bb = 1.54059 \\u00c5) in the 2\\u03b8 range of 10\\u00b0 to 60\\u00b0. The chemical composition of the samples was investigated by XPS (K-alpha, ThermoFisher), while elemental composition distribution measurements were carried out in depth profiling mode using a TOF SIMS 5 (ION TOF) and the thickness of the samples was measured using a surface profiler (KLA Tencor).\\n\\nITO substrates were cleaned using the abovementioned method and treated by a UV/O3 cleaner for 30 min. A poly(3,4-ethylenedioxythiophene):polystyrene sulfonic acid (PEDOT:PSS) layer was deposited on the cleaned ITO substrates by spin-coating at 4000 rpm for 40 s, followed by annealing at 150 \\u00b0C for 15 min. On top of the PEDOT:PSS layer, the perovskite layer of CSA-2 in 1:1 molar ratio was spin-coated at 4000 rpm and annealed at 100 \\u00b0C for 10 min. Then a 100 nm thick TPBi layer was deposited through a shadow mask using thermal evaporation with an active area of 0.130 cm2. Finally, a 100 nm thick Al layer was deposited under vacuum (<106 Torr) using thermal evaporation.\\n\\nDFT calculations were performed using the PBE exchange correlation functional and Tkatchenko\\u2013Scheffler (TS) van der Waals corrections in conjunction with PAW planewave basis sets of 500 eV energy cut-off in a (2 \\u00d7 2 \\u00d7 2) \\u0393-centered k-point mesh for the (3 \\u00d7 3 \\u00d7 3) supercell of cubic CsPbI3 using the VASP suite.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsBa0.1Pb0.9I3,\\n Perovskite_composition_short_form: CsBaPbI,\\n Perovskite_additives_compounds: CSA,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60; 120,\\n Perovskite_deposition_thermal_annealing_time: 1.0; 10.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.13,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"OMOs composed of Ag, Ag(O), TiO2, and ZnO were fabricated at room temperature on 125 \\u03bcm-thick PET (Panac Co., Ltd.) substrates with different structural configurations using a magnetron sputtering system (A-tech System Co.). These multilayer configurations were prepared by sequential sputtering processes without breaking the vacuum conditions. The sputtering processes were initiated once the chamber was evacuated to a base pressure of 7 \\u00d7 10\\u22127 torr. ZnO and TiO2 layers were deposited by sputtering 4-in stoichiometric ZnO and TiO2 targets (Applied Science Co.), respectively, at a radio-frequency power of 200 W and a working pressure of 3 \\u00d7 10\\u22123 torr, which was attained under an Ar atmosphere flowing at 60 sccm. The thicknesses of the bottom oxide layers were fixed at 5 nm, while the thicknesses of the top oxide layers were varied between 10 and 20 nm. The ITO sputtering conditions using a 4-in ITO target with 10 wt% Sn (Applied Science Co.) were identical to those of the oxide layers. Ag was deposited by sputtering a 4-in pure Ag target (Applied Science Co.) at a direct-current power of 50 W and a working pressure of 3 \\u00d7 10\\u22123 torr under an Ar atmosphere flowing at 45 sccm. Ag(O) was deposited under conditions equivalent to those of Ag sputtering except for the mixed atmosphere of Ar and O2 at a flow rate of 45:4 sccm, which generated a reactive sputtering process. The sputtering system and process conditions are demonstrated in detail elsewhere.\\nPSCs were fabricated on PET substrates using different OMO structural configurations: TiO2/Ag/TiO2, TiO2/Ag/ZnO, TiO2/Ag(O)/TiO2, and TiO2/Ag(O)/ZnO. Fabrication was initiated by exposing the OMOs coated on PET substrates to an ultraviolet (UV)-ozone environment for 20 min prior to coating the perovskite precursors on the OMOs. The MAPbI3 perovskite precursor solution was prepared by dissolving 0.461 g of PbI2 and 0.159 g of CH3NH3I (MAI) in a mixed solution of 71 \\u03bcl of dimethyl sulfoxide (DMSO, anhydrous, 99.9%, Sigma-Aldrich) and 635 \\u03bcl of N,N-dimethylformamide (DMF, anhydrous, 99.8%, Sigma-Aldrich). Then, MAPbI3 was deposited from the precursor solution by spin coating followed by a thermal treatment. Specifically, during the spin coating at 4500 rpm for 25 s, the precursor solution was mixed with 700 \\u03bcl of diethyl ether, which was added dropwise. The spin-coated film was sequentially annealed at 60 \\u00b0C for 1 min and 100 \\u00b0C for 5 min. The HTL was prepared by dissolving 72.3 mg of spiro-OMeTAD in a mixture of 1 ml of chlorobenzene, 28.8 \\u03bcl of 4-tert-butylpyridine (96%, Sigma-Aldrich), and 17.5 \\u03bcl of Li-bis(trifluoromethanesulfonyl) imide (Li-TFSI), which was prepared by dissolving 520 mg of Li-TFSI in 1 ml of acetonitrile (99.8%, Sigma-Aldrich). The HTL was spin-coated on the MAPbI3 layer at 4000 rpm for 20 s. Finally, a top electrode based on Au with a thickness of 100 nm was deposited on the HTL by thermal evaporation with a device area of 0.075 cm2. A thin TiO2 layer between the Au rear contact and the Ag TE, as shown in the structural architecture of the PSCs (Fig. 7a), was applied purely to avoid any deterioration in the electrical conductivity due to oxidation of the TE. However, the thickness of the TiO2 layer was selected to be as low as 5 nm to minimize any detrimental increase in the series resistance, due to the insertion of the TiO2 layer.\\n\\nThe morphologies of the Ag and Ag(O) TEs, which evolved from nanoclusters to agglomerates, and the TiO2 ETLs were investigated by capturing top-view and cross-sectional high-resolution images using ultrahigh-resolution FE-SEM (Hitachi High-Technologies Co., S-5500) at the Korea Basic Science Institute (KBSI, Jeonju, Republic of Korea). The distribution of nanoscopic pinholes in the TiO2 ETLs in different OMO structural configurations was determined using AFM (Bruker, Nanoscope V Multimode 8) in the conductive mode at a 600 mV bias. The surface area of pinholes was determined from the FE-SEM images using image processing software (Nikon, NIS-Elements Basic Research). The nominal thicknesses of the metal and oxide layers were determined either using X-ray reflectivity (Philips, X'pert Pro-MRD) at the KBSI in Daegu, Republic of Korea, or surface profiling (Bruker, Dektak XT) measurements at the Korea Institute of Materials Science (KIMS). The dose of oxygen was determined using XPS (Escalab 200 R, VG Scientific) at the Electronics and Telecommunications Research Institute (Daejeon, Republic of Korea). The crystallography of TiO2 and ZnO was characterized using XRD (Empyrean, PANalytical) at the KBSI Daegu. The total (specular + diffusive) transmittance and reflectance spectra were determined using UV-visible spectrophotometry (Agilent Technology, Cary 5000) in the visible spectral range of 330\\u2013800 nm. The absorbance spectra of the OMO structures were determined by ascertaining the transmittance and reflectance spectra. The sheet resistances of OMOs and ITOs were determined by averaging the measurements from three different samples with dimensions of 2.5 \\u00d7 2.5 cm2 using a four-point probe (Hitachi Chemical Co., MCP-T600). The mechanical bending tests were carried out using a homemade bending test system by tracking the increase in the resistance of OMOs and ITOs as a function of the bending radius of PET substrates coated with OMOs and ITOs. The bending radius was decreased to 4 mm to subject the samples to increased tensile stresses. The structural reliability of the samples against repeated deformation was also determined by measuring the change in resistance as the samples were bent cyclically up to 5000 times. The J\\u2013V characteristic of PSCs was measured using a source measurement unit (Keithley 2400 SourceMeter) with a xenon lamp under one-sun conditions and a light intensity of 100 mW cm\\u22122. The light source was calibrated using a modulated silicon solar cell that was certified by the Korea Institute of Energy Research (Taejon, Republic of Korea). The delay between each voltage step was fixed at 200 ms. The EQEs were determined using a Solar Cell Quantum Efficiency Measurement System (PV Measurement) over the wavelength range of 330\\u2013800 nm, and photo signals from the whole range were calibrated with photodiodes.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: PET,\\n ETL_stack_sequence: ZnO-c | Ag | TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Sputtering | Sputtering | Sputtering,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.075,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI) and PCBM were purchased from Xi'an Polymer Light Technology Corp. (China) and Nano-C (USA), respectively. Lead acetate trihydrate (PbAc2\\u00b73H2O), bathocuproine (BCP), and all the solvents [including N,N-dimethylmethanamide (DMF), chlorobenzene (CB), methanol, ethanol, and isopropanol] were purchased from Sigma-Aldrich (USA). The patterned indium tin oxide (ITO) glasses were purchased from Ying Kou You Xuan Trade Co., Ltd (China).\\n\\nPSCs were fabricated on pre-rinsed ITO glass substrates with a structure of ITO/PEDOT:PSS/perovskite (CH3NH3PbI3)/PCBM/BCP/Ag. The perovskite precursor solution was prepared by dissolving PbAc2\\u00b73H2O and MAI (1:3 in molar ratio) in DMF with a concentration of 40 wt%. First, PEDOT:PSS [Clevios P VP AI 4083; molecular structures are shown in Fig. 1(a)] layers of about 40 nm were spin-coated on the ITO glass substrates and annealed at 140 \\u00b0C for 10 min in air. During the alcohol vapor annealing process, 100 \\u03bcL of methanol, ethanol, or isopropanol was added to a Petri dish cover (with a diameter of 14 cm and a height of 2 cm) to form a alcohol atmosphere for SVA, as shown in Fig. 1(b). To fabricate reference devices, this operation was skipped. Then perovskite layers were formed by spin-coating the perovskite precursor solution onto the PEDOT:PSS layer at 4000 rpm for 30 s and annealing at 90 \\u00b0C for 10 min. Next, a PCBM solution (20 mg mL\\u22121 in CB) was subsequently spin-coated onto the perovskite layers at 1000 rpm for 60 s. Finally, BCP (3.5 nm) and Ag (100 nm) were thermally evaporated onto the PCBM layers to complete device fabrication. The effective working area of the PSCs was 0.1 cm\\u22122, which was defined by a shadow mask.\\n\\nThe conductivity of the PEDOT:PSS layers was measured using a four-point probe system with a current source-meter (Keithley 2400, USA). The thickness of the PEDOT:PSS layer was measured using a surface profilometer (Dektak 150, Veeco, USA). The transmittance and absorbance spectra were obtained using ultraviolet\\u2013visible (UV\\u2013vis) spectroscopy (PerkinElmer Lambda 750, USA). Topographic images of the layers were acquired using an AFM (Veeco, USA) in tapping mode. Cross-sectional and top-view scanning electron microscopy (SEM) images were obtained using an SU8020 instrument (Hitachi, Japan) operated at an acceleration voltage of 8 kV. The photoluminescence (PL) and time-resolved photoluminescence (TRPL) spectra were obtained using a spectrometer (FLS920, Edinburgh Instruments, UK). The current density\\u2013voltage (J\\u2013V) characteristics of the PSCs were measured at an irradiation intensity of 100 mW cm\\u22122 (AM1.5). The incident-photon-to-current efficiency (IPCE) spectra were obtained using a Solar Cell IPCE measurement system (Solar Cell Scan 100, Zolix, China).\\n\\nThe effects of alcohol vapor annealing were theoretically investigated using dissipative particle dynamics implemented in the Mesocite module of the Materials Studio (MS) 8.0 software. A cubic supercell with lateral dimensions of 100 \\u00c5 \\u00d7 100 \\u00c5 \\u00d7 100 \\u00c5 was employed in the simulations and contained 9260 PEDOT:PSS monomers and 1389 alcohol molecules. The average densities of PEDOT and PSS were set to 1.34 and 1.16 g cm\\u22123, respectively. Newton's equation of motion was integrated using the Verlet algorithm with a time step of 1 fs. The ratio of the simulated PEDOT and PSS monomer beads was set to 1:3, which is similar to the results of the X-ray photoelectron spectroscopy (XPS) measurement and previous work. The simulated temperature and pressure were set at 413.15 K (140 \\u00b0C) and 101.325 kPa (1 atm), respectively.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials, including methylammonium iodide (MAI, 99.8%, Dyesol), formamidinium iodide (FAI, 99.8%, Dyesol), lead iodide (PbI2, 99.999%, Sigma), lead chloride (PbCl2, 99.999%, Alfa), bathocuproine (BCP, 96%, Sigma), nitrate hexahydrate (Ni(NO3)\\u00b76H2O, 99.999%, Sigma), 2-methoxyethanol (99.8%, Sigma-alsrich), acetylacetone (95%, Fuchen), chlorobenzene (CB, 99.8%, Sigma), N,N\\u2032-dimethylformamide (DMF, 99.8%, Sigma), isopropanol (IPA, 99.5%, Sigma), and phenyl-C61-butyric acid methyl ester (PC61BM, 98%, Nano-c) were used as received without further purification.\\n\\nIn order to prepare NiOx solution, Ni(NO3)2\\u00b76H2O (1 mol) was dissolved in 2-methoxyethanol solution (10 ml) at 50 \\u00b0C by stirring for 1 h, and then 100 \\u03bcl acetylacetone was added to mix all night at room temperature. To make a perovskite layer, a perovskite precursor solution consisting of 1.36 mol PbI2 and 0.24 mol PbCl2 in the solvent DMF was stirred for 2 h at 72 \\u00b0C, and 70 mg MAI and 30 mg FAI were dissolved in the solvent IPA for later use. Next, MAI (0 mg ml\\u22121 in IPA, 2 mg ml\\u22121 in IPA, 4 mg ml\\u22121 in IPA), PCBM (20 mg ml\\u22121 in CB) and BCP (0.5 mg ml\\u22121 in IPA) were prepared for next use.\\n\\nA p-i-n planar PSC was fabricated on pre-patterned ITO (indium tin oxide) glass substrates (around 2 \\u00d7 2.5 cm2 in size, 10 \\u03a9 per square). The ITO glass substrates were ultrasonically cleaned with a detergent, deionized water, acetone, and ethanol for 30 min, respectively. Then, ITO glass substrates were treated in a UV-ozone system for 30 min to remove organic materials from the surface and improve the hydrophilicity. NiOx films were spin-coated at 3000 rpm for 45 s and annealed at 250 \\u00b0C for 45 min on a hotplate. The two-step sequential deposition of the perovskite, which is widely used in PSCs, provides a low cost and efficient route to prepare perovskite films. Fig. 1 shows the strategy for the preparation and the treatment used in this work. Briefly, PbI2 and PbCl2 are dissolved in DMF solution and spin-coated on the NiOx layer with a speed of 3000 rpm and a time of 45 s as shown in Fig. 1(a). Fig. 1(b) shows that MAI and FAI were dissolved in IPA solution and then spin-coated at 3000 rpm for 45 s. The device was annealed at 104 \\u00b0C for 10 min on a hotplate (Fig. 1(c)) so that the perovskite film could be formed by the inter-diffusion approach. In the conventional device fabrication, the perovskite film preparation has no further steps. However, we will use a facile way to further treat the film and improve the material quality. As shown in Fig. 1(d), the perovskite film is post-treated with the MAI/IPA solution after the film has been formed. MAI of different quantities was dissolved in IPA to prepare the solution (0 mg ml\\u22121 MAI, 2 mg ml\\u22121 MAI, and 4 mg ml\\u22121 MAI). Then the MAI/IPA solution was spin coated on the perovskite films at 3000 rpm for 45 s as in figure (d). Figure (e) shows that post-treated films were formed after annealing at 104 \\u00b0C for another 10 min. Then, the prepared perovskite films were covered with PC61BM. PC61BM was spin-coated at 2000 rpm for 45 s. Next, BCP films were spin-coated at 6000 rpm for 45 s. The thickness of the PCBM film was about 50 nm. The thin layer of BCP (0.5 mg ml\\u22121 in IPA) was deposited on the top of the PCBM layer at 6000 rpm for 40 s. Finally, the films were transferred to a metal evaporation chamber, and 100 nm thick Ag contacts were deposited under high vacuum (<4 \\u00d7 10\\u22124 Pa). The active area was 0.07 cm2 defined by a shadow mask. The finished device in this work is shown in Fig. 1(f), which is an inverted p-i-n planar heterojunction structure. The schematic structure of the device is glass/ITO/NiOx/CH3NH3PbIxCl3\\u2212x/PC61BM/BCP/Ag. Here, NiOx and PCBM act as the HTL and ETL, respectively. BCP is used as the hole blocking layer and interface modification layer. The ITO and the Ag films act as the bottom and top transparent electrodes.\\n\\nPhotocurrent density versus voltage (J\\u2013V) curves were acquired using a solar simulator (Sanei Electric, XES-300T1) with a Keithley 2400 source meter and an AM 1.5 G filter with an intensity of 100 mW cm\\u22122. The system was calibrated against a NREL certified reference solar cell. The incident photon conversion efficiency (IPCE) was measured using a quantum efficiency measurement system (SCS10-X150, Zolix instrument. Co. Ltd). The UV-VIS system (PerkinElmer Lambda 950, Waltham, MA) was used to measure absorption. TPC measurement was performed with a system excited with a 532 nm pulse laser (MPL-H-532). TPV measurement was performed with the same system excited with a 405 nm CW laser (MDL-III-405) modulated by a square signal (200 Hz, 5 ms) generated by an arbitrary function generator (Tektronix, AFG3051C). A digital oscilloscope (Tektronix, MSO5204B) was used to record the photocurrent or photovoltage decay process with a sampling resistor of 50 \\u03a9 or 1 M\\u03a9, respectively. The film morphology was characterized using a JSM-7800F extreme-resolution analytical field emission scanning electron microscope (SEM) and atomic force microscope (AFM) (Agilent 5500, Santa Clara, CA, USA). XRD spectra were obtained by probing samples with an X-ray diffractometer. All measurements of the solar cells were performed under ambient atmosphere at room temperature without encapsulation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 104.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The GZO films were deposited from a GZO target (purchased from Zhongnuo material Co., Ltd. China) on FTO substrates by RF magnetron sputtering at room temperature. Before sputtering, the substrates were ultrasonically cleaned with distilled water, acetone, and ethanol, respectively. The atomic ratio of Ga to Zn in the GZO film is 5:95. Before deposition, the pressure in chamber was adjusted to 4 \\u00d7 10\\u22124 Pa, high purity (99.999%) Ar gas with 30 sccm was introduced through a mass flow controller. During the deposition, the chamber pressure, RF power, and deposition time were adjusted to be 0.6 Pa, 100 W, and 2 min, respectively.\\n\\nGZO films were laser-annealed by irradiating the surface of the film with a XeCl (308 nm) excimer laser in air at room temperature. The thickness of the films were measured with a step profiler and found to be approximately 36 nm, a schematic of the excimer laser anneal system is shown in Fig. 1. A laser beam with an energy of 200 mJ was irradiated onto the films after focussing. The repetition rate of the laser pulse is 1 Hz. The energy density can be calculated by dividing the laser energy by the irradiating area. By adjusting the distance between the film and focusing lens, the effective area changes, thus different energy densities of 105, 90, 75, and 60 mJ cm\\u22122 were obtained. The pulse count was adjusted to 1, 5, 10, 20, 30, and 40, respectively. The samples under different treatment conditions are labelled as ELA (energy density)-(pulse number). The as-prepared GZO films without any treatment (NG) as well as heated to 500 \\u00b0C in air (HG), prepared according to pervious report, were employed for comparison. To ensure the reproducibility for the data 6 samples are included in each group.\\n\\nThe GZO films with different treatments were used as ETLs in PHJ-PSC. One-step method was applied for the fabrication of the perovskite layer. Specifically, PbI2 (477 mg) and methylammonium iodide (MAI, 160 mg) were dissolved in N,N-dimethylformamide (DMF, 0.64 mL) and N,N-dimethylsulfoxide (DMSO, 0.16 mL) to form the precursor solution. The solution (40 \\u03bcL) was spin-coated on the GZO films at 1000 rpm for 3 s, then 4000 rpm for 12 s, chlorobenzene (CB, 0.3 mL) was uniformly dripped onto the rotating substrate in 10 s at 4000 rpm. The formed MAPbI3 films were heated at 70 \\u00b0C for 10 min. The hole transport layer (solution of Spiro-OMeTAD in chlorobenzene with additive according to the previous report ) was spin-coated on the MAPbI3 films at 4000 rpm for 30 s. Finally, 60 nm of Au electrode was deposited on the hole transport layer via vacuum thermal evaporation. For comparison, ZnO ETLs prepared by magnetron sputtering (HZ) followed by 500 \\u00b0C of heat treatment were also used to fabricate PHJ-PSCs employing the same fabrication process.\\n\\nThe crystal structure of the films was investigated by X-ray diffraction (XRD, Philips X'pert diffractometer, Holland) with Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5). The morphology of the films was determined using a field-emission scanning electron microscope (FE-SEM, FEI Sirion-200, USA) and an atomic force microscope (AFM, CSPM-5500, China). A step profiler (XP-2, AMBIOS Technology Inc., USA) was used to measure the film thickness. The optical transmittance and absorption spectra of the films were determined by UV-visible spectrophotometry (U-3900H, Japan) in the wavelength range 200 to 900 nm. The resistivity was measured by the standard four probe d.c. method using a Keithley 2420 digital source meter.\\nThe photocurrent\\u2013photovoltage (J\\u2013V) curves of the PHJ-PSCs were measured with a Keithley 2420 digital source meter under irradiation of a solar simulator (Newport Oriel 94043A, USA, AM 1.5, 100 mW cm\\u22122). The monochromatic incident photon to electron conversion efficiency (IPCE) spectra were determined employing a 300 W Xe lamp light source with monochromatic light in the range 300 to 900 nm. Electrochemical impedance spectroscopy (EIS) was conducted on a frequency response analyzer (Zahner, Zennium, Germany), the cells were measured under the bias voltages of 0.8 V in the dark, the frequency range was 1 to 106 Hz, and the magnitude of the alternative signal was 10 mV. The photoluminescence (PL) spectra of the perovskite films were obtained using an Edinburgh FLSP920 spectrometer (UK) with an excitation xenon lamp source. The transient absorption spectra (TAS) of the perovskite films were acquired using laser flash photolysis spectrophotometry (LKS80, UK), the energy of the laser device was 150 mJ cm\\u22122 and the repetition rate was 5 Hz. The wavelength of the excitation and probe light were 473 and 770 nm, respectively.\\n\\nSimulations of the ELA process was performed using ANSYS\\u00ae software. The irradiation area of the incident light is large than the substrate and the absorbed power transferred from the laser is symmetrically distributed along the axial axis.\\nTherefore, the model can be regarded as a heat flux caused by laser irradiation on a two dimensional finite element film along the thickness orientation, building on the basis that the phase transition does not take place. The thickness of the films and glass substrate was set as 36 nm and 360 nm, respectively. The energy of laser beam is viewed as the absorption in the form of heat, which follows a top Gauss distribution, and the relation between the heat flux and energy density can be described as follows:\\nwhere Q is the heat flux, R is the light reflection coefficient of films to the laser, E is the energy density and P is the width of single pulse. Herein, R is set as 0.4, P equals 20 ns, and the values used in simulation are given in Table S1.\\u2020\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Magnetron sputtering,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Formamidinium iodide HC(NH2)2I (FAI) was synthesized by reacting 30 mL hydroiodic acid (57 wt% in water, Sigma-Aldrich) with 15 g of formamidinium acetate (99%, Aldrich) at 0 \\u00b0C. After stirring for 2 h, a dark yellow precipitate was recovered by evaporating the solvent at 60 \\u00b0C using a rotary evaporator. The solid was washed with diethyl ether and then recrystallized from ethanol. The white precipitate was dried under vacuum for 24 h and stored in a glove box filled with Ar. All the chemicals were used as received without further purification.\\n\\nPerovskite solar cells were fabricated in ambient conditions, in which the relative humidity was not controlled. FTO glass substrates (Pilkington, TEC-8, 8 \\u03a9 sq\\u22121) were cleaned with a detergent, deionized water, and acetone, followed by sonicating with ethanol in an ultrasonic bath for 20 min. Ultraviolet-ozone (UVO) was treated for 15 min prior to use. The precursor solutions for the SnO2 ETL were prepared by dissolving tin(IV) isopropoxide (Alfa Aesar, 10% w/v in isopropanol (IPA), 99%) in IPA, where the solution concentration was varied from 0.05 M to 0.20 M. The precursor solution was spin-coated on FTO glass in a glove box filled with N2 at a spinning rate of 5000 rpm for 20 s, which was dried at 65 \\u00b0C on a hotplate for 1 min. The pre-dried SnO2 films were heated further in the furnace at ambient conditions at different temperatures of 100 \\u00b0C, 150 \\u00b0C, 200 \\u00b0C, 250 \\u00b0C, 300 \\u00b0C, 350 \\u00b0C, 400 \\u00b0C and 500 \\u00b0C for 30 min. To improve the adhesion of SnO2 layers on FTO, bare FTO glasses were treated with UV ozone for 20 min before and after coating the SnO2 precursor solution. After cooling to room temperature, the substrate coated with SnO2 film was exposed to UVO for 20 min prior to coating the perovskite film. For the perovskite composition, we considered efficient charge extraction from the perovskite to SnO2. Better charge extraction was proposed for the mixed cation perovskite rather than pure CH3NH3PbI3. We designed a composition of (FAPbI3)0.875(CsPbBr3)0.125 that was prepared for a SnO2-based planar perovskite solar cell. The perovskite precursor solution was prepared by mixing 0.1504 g of FAI, 0.4034 g of PbI2, 0.0459 g of PbBr2, and 0.0266 mg of CsBr in DMF based on the ratio of (PbI2 + PbBr):DMSO:(FAI + CsBr) = 1:1:1. The solution concentration was 54 wt%. The completely dissolved solution was spin-coated on the SnO2 film at 4000 rpm for 20 s, in which 0.5 mL of diethyl ether was dripped on the rotating substrate to induce an intermediate for preparation of the adduct. The perovskite films were formed after heating at 145 \\u00b0C for 40 min. Spiro-MeOTAD was used as the HTL and formed on top of the perovskite layer. The 20 \\u03bcL of spiro-MeOTAD solution, which consisted of 50.6 mg spiro-MeOTAD, 20.16 \\u03bcL of 4-tert-butyl pyridine (TBP) and 12.25 \\u03bcL of lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) solution (520 mg LiTSFI in 1 mL acetonitrile) in 0.7 mL of chlorobenzene, was spin-coated on the perovskite layer at 3000 rpm for 30 s. Finally, the Au electrode was deposited using a thermal evaporator at a constant evaporation rate of 0.05 nm s\\u22121.\\n\\nThe current density\\u2013voltage (J\\u2013V) and current density\\u2013time (J\\u2013t) curves were measured under AM 1.5G one sun illumination (100 mW cm\\u22122) using a solar simulator (Oriel Sol, 3A class) equipped with a 450 W xenon lamp (Newport 6279NS) and a Keithley 2400 source meter. One sun light intensity was adjusted using the NREL-calibrated Si solar cell having a KG-5 filter. The device was covered with a metal aperture with an active area of 0.125 cm2 during the measurement. The external quantum efficiency (EQE) was measured by a specially designed EQE system (PV measurement Inc.), in which a monochromatic beam was generated from a 75 W xenon source lamp (USHIO, Japan). EQE data were collected in the DC mode without light bias. Absorption and transmittance spectra of the SnO2 films were measured using a UV-vis spectrometer (Agilent 8453). Plane-view and cross-sectional morphologies were investigated by scanning electron microscopy (SEM) (JSM7000F, JEOL). The thicknesses of SnO2 films were measured by SEM. X-ray diffraction (HD-powder XRD-D8 Advance, Bruker) was used to study the crystal structure of the SnO2 films, in which Cu K\\u03b1 radiation was used (\\u03bb = 1.5406 \\u00c5) and the scan rate was 5\\u00b0 min\\u22121. The binding energy and oxidation state were investigated using X-ray photoelectron spectroscopy (XPS, ESCALAB250Xi, Thermo UK) with monochromatic Al K\\u03b1 generating a 1486.7 eV X-ray source. The electron take-off angle was fixed at 0\\u00b0 and the vacuum pressure was below 1 \\u00d7 10\\u22129 mbar. The binding energy scale was calibrated using the hydrocarbon contamination on the surface based on the C 1s peak at 284.8 eV. The work function was investigated using ultraviolet photoelectron spectroscopy (UPS, ESCALAB250Xi, Thermo UK) using the He I (21.22 eV) emission line. Time-integrated and time-resolved photoluminescence (PL) were measured by a Quantaurus-Tau compact fluorescence lifetime spectrometer (Quantaurus-Tau C11367-12, Hamamatsu). The film samples were excited with a 464 nm laser (PLP-10, model M12488-33, peak power of 231 mW and pulse duration of 53 ps, Hamamatsu) pulsed at a repetition frequency of 10 MHz for time-integrated and 2 MHz for time-resolved PL. Impedance spectroscopy (IS) measurements were carried out using a PGSTAT 128N device (Autolab, Eco-Chemie) with a small perturbation AC 20 mV sinusoidal signal on the DC voltage from 0 V to 0.8 V and frequency ranging from 1 MHz to 0.1 Hz. The measured Nyquist plots were fitted using Z-View software using an equivalent circuit composed of series resistance (Rs) and two R\\u2013C components (resistance and capacitance in parallel) in series. Conductive atomic force microscopy (C-AFM) was used to study the surface conductivity of the deposited SnO2 films. A commercial atomic force microscopy system (SPA-400, SII, Japan) was employed using Pt/Ir-coated Si tips (CONTPt, Nanoworld, Switzerland) with a typical resonant frequency of 13 kHz and a spring constant of 0.2 N m\\u22121. All the images were acquired with a contact force of \\u22121.5 nN, and bias voltages of 0.1\\u20130.5 V at a scan rate of 1.0 Hz. Negative biases were applied to the substrate, while the tip was grounded. The current and topographic images were obtained under ambient conditions, simultaneously.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.125FA0.875PbBr0.375I2.625,\\n Perovskite_composition_short_form: CsFAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 145,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.125,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI) and lead chloride (PbCl2) were purchased from Yingkou Optimal Choice Trade, China. [6,6]-Phenyl-C61-butyric acid methyl was purchased from American Dye Source. The bis-functional of C70 (C70-bis) was purchased from 1-Material, Canada. N,N-Dimethylformamide (DMF) was purchased from Aldrich company. Isopropanol (IPA) and toluene (TOL) were purchased from Beijing Chemical Factory, China. The materials were used without further purification.\\n\\nDuring the solvent vapor annealing process, the active layer was placed into a glass tube which contained toluene, isopropanol and DMF at the bottom, respectively. Stable vapor gradient along the tube could be obtained after 15 min since the liquid solvent location was fixed. The vapor pressure of the sample was P = 0.54 (25 \\u00b0C). (The length of the tube is 3 cm and the liquid height is 0.2 cm. The solvent vapor pressure P is given by P = L/L0, where L is the distance from the up edge of the setup to the specimen position and L0 is the length given by the distance from the up edge of the setup to the surface of the solvent at the bottom of the tube). The samples of toluene, isopropanol and DMF were treated under this vapor pressure for 180 s, 120 s and 20 s, respectively, as the active layer was spin-coated.\\n\\nThe devices were fabricated in the configuration of indium tin oxide (ITO)/PEDOT:PSS/CH3NH3PbI3\\u2212xClx/[6,6]-phenyl-C61-butyric acid methyl ester (PC61BM)/fullerene surfactant (C70-bis)/Al. The ITO glass substrates were cleaned sequentially with detergent and deionized water, acetone, and isopropanol under sonication for 10 min. After drying under a nitrogen flow, substrates were treated with UV-ozone for 25 min. The poly(ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, Baytron P4083, filtered through a 0.45 \\u03bcm nylon filter) layer was first spin-coated at 5k rpm for 40 s on this well-cleaned ITO glass and dried at 140 \\u00b0C in a vacuum for 30 min. The substrates were transferred into a N2-filled glovebox, where the thin-film perovskite layers were spin-coated from a homogeneous 30 wt% (PbCl2:MAI with a molar ratio of 1:3 in DMF) precursor solution at 7k rpm for 45 s (300 nm thickness) on the hot substrates (about 63 \\u00b0C) and then annealed at 75 \\u00b0C for 5 h. Afterward, the PC61BM (15 mg mL\\u22121 in chloroform) and C70-bis surfactant (2 mg mL\\u22121 in isopropyl alcohol) were then sequentially deposited by spin coating at 3k rpm for 60 s, respectively. Finally, a layer structure of Al (90 nm) was deposited at the top of the active layer by thermal evaporation in a vacuum of 2 \\u00d7 10\\u22124 Pa to complete the device fabrication.\\n\\nThe morphology of hybrid perovskite films was acquired by field-emission scanning electron microscopy (FESEM) using a Micro FEI Philips XL-30-ESEMFEG microscope at an accelerating voltage of 20 kV. The sample was sputter coated with gold before SEM observation. The elemental distribution of the film was analyzed using energy dispersive spectroscopy (EDS, GENESIE 2000-EDAX).\\nThe crystallinity of the perovskite film was analyzed using out-of-plane grazing incidence X-ray diffraction (GIXD) measurements, two-dimensional GIXD (2D GIXD). The GIXD profiles were obtained by using a Bruker D8 Discover reflector with an X-ray generation power of 40 kV tube voltage and 40 mA tube current. The measurements were achieved in a scanning interval of 2\\u03b8 between 3 and 60\\u00b0. The 2D GIXD profiles were obtained by using a Rigaku Smartlab instrument with an X-ray generation power of 40 kV tube voltage and 30 mA tube current and BL14B1 at Shanghai Synchrotron Radiation Facility (SSRF; \\u03bb = 0.124 nm).\\nThe photon absorption of the active layer and situ absorption spectrum was recorded by combining UV-vis absorption spectroscopy (Shimadzu UV 3600 spectrophotometer in a spectral range of 300\\u20131000 nm) with a home-made heater.\\nTo demonstrate the orientation evolution, situ 2D GIXD was operated through combining Rigaku SmartLab instrument with an X-ray generation power of 40 kV tube voltage and 30 mA tube current with a home-made heater. The perovskite film without solvent vapor treatment was annealed at 65 \\u00b0C and the film with solvent vapor treatment was annealed at 75 \\u00b0C under vacuum.\\nCurrent density\\u2013voltage (I\\u2013V) characteristics of the PV cells were measured using a computer controlled Keithley 236 source meter under AM1.5G illumination from a calibrated solar simulator with an irradiation intensity of 100 mW cm\\u22122. The device area was 12 mm2, determined by the overlap of the cathode and anode. An aperture size of 10.6 was used to define the light absorption area, which would avoid the overestimation of the photocurrent density by the optical pining effect.\\nNanosecond fluorescence lifetime experiments were performed using the time-correlated single-photon counting (TCSPC) system under right-angle sample geometry. A 400 nm picosecond diode laser (Edinburgh Instruments EPL375, repetition rate 20 MHz) was used to excite the samples. The fluorescence was collected by using a photomultiplier tube (Hamamatsu H5783p) connected to a TCSPC board (Becker & Hickl SPC-130). The time constant of the instrument response function (IRF) is about 220 ps.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | bis-C70,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 75,\\n Perovskite_deposition_thermal_annealing_time: 300,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped tin oxide (FTO) glass (Pilkington, TEC15) was etched with Zn powder and HCl aqueous. The etched glass was then cleaned with detergent, distilled water, and ethanol. The blocking TiO2 layers (bl-TiO2) were deposited on the as-prepared FTO by means of spray pyrolysis followed by calcination at 510 \\u00b0C for 30 min. The mesoporous TiO2 (mp-TiO2) film was deposited on cooling bl-TiO2 by spin-coating of the TiO2 paste (Dyesol 30NR-T) which was followed by heating at 510 \\u00b0C for 20 min. During the single-step deposition process, the precursor solution (461 mg of PbI2, 159 mg of CH3NH3I, and 78 mg of DMSO in 600 mg of DMF) was spin-coated on the substrates at 4000 rpm for 25 s and 0.5 ml of diethyl ether was dripped on the substrate within 10 s before the surface changed to be turbid. For depositing the MAPbI3 perovskite layer with large grains, first a layer of Pb3I8 was spin-coated on the prepared mp-TiO2 layer from PbI2:MAI:DMSO precursor solution (461 mg of PbI2, 106 mg of CH3NH3I, and 78 mg of DMSO in 600 mg of DMF) at 3000 rpm for 20 s, then a 50 mg mL\\u22121 of MAI in IPA solution was spin coated on the Pb3I8 film at 3000 rpm for 20 s immediately. The deposited perovskite film was heated at 105 \\u00b0C for 30 min to obtain a dense film. Then, 35 \\u03bcL of spiro-OMeTAD solution, which contained 73 mg of spiro-OMeTAD, 28 \\u03bcL of 4-tert-butyl pyridine and 17.5 \\u03bcL of lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg of Li-TSFI in 1 mL of acetonitrile) in 1 mL of CBZ, was spin-coated on the perovskite film at 3000 rpm for 20 s. Finally, a \\u223c60 nm gold electrode was deposited via thermal evaporation under vacuum at a constant evaporation rate of 0.6 nm s\\u22121.\\n\\nThe field emission scanning electron microscope (FESEM, FEI Sirion 200, Netherlands) was used to study the top-morphology of the prepared film. The crystal phase was obtained by X-ray diffraction (X'Pert Pro, Netherlands) using a Cu K\\u03b1 beam (\\u03bb = 1.54 \\u00c5). The photocurrent density\\u2013voltage (J\\u2013V) curves were measured under one sun illumination (AM 1.5G, 100 mW cm\\u22122) with a solar simulator (94043A, USA) equipped with a Keithley 2400 source meter. When measuring, a mask with 0.09 cm2 aperture area was used to avoid light scattering through the sides and to define the effective area of the device. Ultraviolet\\u2013visible (UV\\u2013vis) diffuse reflectance spectroscopy and absorption spectroscopy were performed using the UV\\u2013vis spectrophotometer (SOLID3700, Shimadzu Co. Ltd, Japan). Incident photon-to-electron conversion efficiency (IPCE) spectra were obtained with a spectral resolution of 5 nm, using a 300 W xenon lamp and a grating monochromator equipped with order sorting filters (Newport/Oriel). The electrochemical impedance spectra (EIS) were obtained on a computer controlled potentiostat (Autolab 320, Metrohm, Switzerland) in a frequency range of 10 mHz\\u20131000 kHz applied in the dark. The micrographs were obtained during cooling between crossed polarizers using a microscope (DM2500P, Leica, Germany) equipped with a hot-stage (LTSE-420, Linkam, UK) and a camera (Micropublisher 5.0 RTV, Qimaging, Canada).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 105,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Tin chloride pentahydrate (SnCl4\\u00b75H2O, AR, 99%), sodium borohydride (NaBH4, 98%), tetramethylammonium hydroxide solution (TMAH, 10% in water) and ethanol (AR) were purchased from Aladdin. N,N-Dimethylformamide (DMF, anhydrous, 99.8%), dimethyl sulfoxide (DMSO, GC, \\u226599.5%), bis(trifluoromethane) sulfonimide lithium salt (LTFSI, 99.95% trace metals basis), potassium iodide (KI, 99.998%), acetonitrile (anhydrous, 99.8%), 4-tert-butylpyridine (4-TBP, 96%) and chlorobenzene (CB, anhydrous, 99.8%) were purchased from Sigma Aldrich. Lead(II) iodide (PbI2, 99.9985%), lead(II) bromide (PbBr2, 99.999%), and SnO2 (Alfa Aesar, 15% in H2O colloidal dispersion) for the control samples were purchased from Alfa Aesar. CH3NH3I (MAI), NH2CHNH2I (FAI) and CH3NH3Br (MABr) were purchased from Dyesol. Spiro-OMeTAD was purchased from Shenzhen Feiming Technology. All chemicals were used as received.\\n\\nSnO2 nanoparticles were synthesized according to a previous report. Briefly, 0.242 g SnCl4\\u00b75H2O was first dissolved in 50 mL DI water (18 M\\u03a9) under stirring for 5 min, which was denoted as solution A. Simultaneously, 0.05 g NaBH4 was dissolved in 20 mL DI water and denoted as solution B. Then solution B was added drop-wise to solution A. The obtained mixture underwent severe stirring at room temperature for about 2 h. During the reaction, the color of the solution turned from grey to white, suggesting the formation of SnO2 nanoparticles. As the reaction finished, the nanoparticles were collected by centrifuging and washed with DI water. The centrifuging and washing processes were repeated 3 times. The collected nanoparticles were diluted to be around 4 mg mL\\u22121 in water to complete the preparation of the n-SnO2 colloidal solution. For the TMAH-modified SnO2 (TMAH-SnO2) colloidal solution, various volumes of TMAH solution (TMAH, 10 wt% in water) were added to the obtained n-SnO2 colloidal solution and stirred for 5 min at room temperature. The added TMAH was varied from 0%, 0.5%, 1%, and 1.5% to 2% in volume ratio (TMAH solution: n-SnO2 solution).\\n\\nAn FTO/ITO glass sheet was sequentially cleaned with detergent (Micro-90, 2% in water), acetone, ethanol and DI water for 30 min. Before deposition of SnO2 thin films, the cleaned FTO was treated with ozone plasma for 15 min. The SnO2 thin films were spin-coated onto the FTO at 2000 rpm for 30 s, and the obtained electrodes were annealed at various temperatures (100 \\u00b0C, 125 \\u00b0C, 150 \\u00b0C, and 175 \\u00b0C) for 30 min. Then the thin films were cooled down to room temperature naturally. Perovskite layers were deposited onto the SnO2-coated FTO directly by spin coating the precursor using the anti-solvent process. The perovskite precursor solution was first prepared by mixing FAI, MAI, PbI2 and PbBr2 in DMF and DMSO (1.25 M with respect to Pb, DMF:DMSO = 4:1). 1% KI doping (K:Pb atom ratio in solution) is achieved by adding KI solution in DMF to the perovskite precursor solution (0.1 M). The stoichiometric composition of the precursor is FA0.75MA0.25PbI2.5Br0.5. Before spin coating, the precursor was filtered with a 0.2 \\u03bcm syringe filter. The perovskite precursor was first spin-coated at 1000 rpm for 10 s, and the spin rate was increased to 3000 rpm for another 30 s. During the second step of spin coating, CB was poured onto the substrate. After spin coating, the electrode was moved to a hot plate at 100 \\u00b0C for 60 min, in order to remove the solvent and for the perovskite crystal growth. The spiro-OMeTAD (80 mg mL\\u22121 in CB) solution with LTFSI (9.1 \\u03bcg mL\\u22121) and 4-TBP (28.5 \\u03bcL mL\\u22121) was then deposited onto the perovskite layer at 4000 rpm for 30 s. Finally, a 100 nm-thick gold electrode was deposited using a thermal evaporator at a rate of 0.1 nm s\\u22121. The active area of the device was determined to be 0.09 cm2 using the mask on the top of the substrate during thermal evaporation.\\n\\nTransmission electron microscopy (TEM) images were taken with a field emission transmission electron microscope (FE-TEM, JEM-2100F) operating at 200 kV accelerating voltage. The morphologies of the SnO2 layer and the perovskite layer were characterized using a scanning electron microscope (SEM, FEI). The conductivity of the thin films was studied by using a conductive atomic force microscope (c-AFM, Bruker) in TUNA mode. The steady state and time-resolved photoluminescence spectra of the perovskite films were measured using a 1/4 m monochromator (Cornerstone\\u2122 260) equipped with a silicon charge-coupled device (CCD) camera. A continuous wave laser (405 nm, 50 mW) was used as the excitation source, and luminescence was detected using the CCD. Ultraviolet photoelectron spectroscopy (UPS) was carried out on a Thermo Scientific ESCALab 250Xi, with the HeI (21.22 eV) emission line employed for excitation. The data were acquired at a bias of \\u221210 V. The work function of the measured samples can be calculated from the following equation: h\\u03bd = EFermi \\u2212 Ecutoff, here, h\\u03bd = 21.22 eV and EFermi = 21.08 eV (using Ni as the standard sample for calibration). The J\\u2013V measurements were carried out in ambient air with a Keithley-2400 source meter under simulated AM 1.5 G illumination (100 mW cm\\u22122, Oriel Sol1A Class ABB Solar Simulator). The light intensity was calibrated with a silicon reference cell (NREL) equipped with a power meter. The devices are measured in the reverse scan (1.2 V to \\u22120.20 V, 0.01 V per step). For hysteresis studies, forward scans (\\u22120.2 V to 1.2 V, 0.01 V per step) were also taken. The delay time has been selected from 1 ms to 1000 ms. IPCE measurements were carried out using an Enli Tech (Taiwan) EQE measurement system.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.75MA0.25PbBr0.5I2.5,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"ZnO (ZnO-350, Sumitomo Osaka Cement Co.) nanoparticles were used as received. Lead iodide (beads, 10 mesh, 99.999% trace metals basis) and lithium salts (>99.0%) were purchased from Aldrich. CH3NH3I (>99.0%) was purchased from Xi'an Polymer Light Technology Co. (PLT). HC(NH2)2I (>98.0%) was purchased from TCI. Spiro-OMeTAD (2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene, >99.0%) was purchased from Merck. Ultradry solvents of N,N-dimethyl formamide (DMF, >99.9%) and isopropanol (>99.9%) were obtained from J&K and Acros, respectively. All the chemicals and solvents were kept in the glove-box before starting our experiment.\\n\\nThe pre-patterned ITO substrates were cleaned with detergent, deionized water, acetone, and 2-propanol in sequence. ZnO nanoparticles were dispersed in butanol at a concentration of 6 mg mL\\u22121 and stirred for 3 hours before use. The solution was filtered with a PVDF hydrophobic 0.45 \\u03bcm filter and spin-coated on ITO substrates at 2500 rpm for 30 s to form a relatively compact ZnO thin layer followed by short baking at 150 \\u00b0C for 5 min. This procedure was repeated three times before finally baking at 200 \\u00b0C for 1 hour. A 460 mg mL\\u22121 solution of PbI2 in DMF was then spin-coated on top of the ZnO layer at 4000 rpm for 30 s in the glove-box. The PbI2-coated ZnO thin film was immediately placed in a covered Petri dish for the SVA process for about 5 minutes followed by annealing at 70 \\u00b0C for 30 min. The films were preheated at 100 \\u00b0C for 3 min before dipping into a FAI 2-propanol solution (10 mg mL\\u22121) for 50 s followed by annealing at 145 \\u00b0C for 15 min to obtain the desired crystallite formation. As the hole-transporting material (HTM), a spiro-OMeTAD solution (80 mg of spiro-OMeTAD, 10.5 \\u03bcL of 4-tert-butylpyridine (tBP), and 46.5 \\u03bcL of a lithium-bis(tri-fluoromethanesulfonyl)imide (Li-TFSI) solution (170 mg Li-TFSI/1 mL acetonitrile) in 1 mL chlorobenzene) was spin-coated at 4000 rpm for 30 s on FAPbI3. The substrates with HTM were left overnight in dry air in the dark at room temperature. Finally, a 60 nm thick Ag electrode was thermally evaporated on top of the HTM to produce a completed PSC device.\\n\\nThe current\\u2013voltage characteristics of solar cells were measured by a computer-controlled Keithley 2400 source meter measurement system with an AM 1.5G filter at a calibrated intensity of 100 mW cm\\u22122 illumination, as determined by a standard silicon reference cell (91150 V Oriel Instruments). The effective area of the cell was defined to be 0.04 cm2 using a non-reflective metal mask. IPCE spectra were measured in air under short-circuit conditions using a commercial IPCE setup (Crowntech QTest Station 1000AD), which was equipped with a 100 W Xe arc lamp, filter wheel, and monochromator. Monochromated light was chopped at a frequency of 80 Hz and photocurrents were measured using a lock-in amplifier. The setup was calibrated against a certified silicon reference diode. The impedance spectroscopy measurement was carried out by a VSP multichannel potentiostatic\\u2013galvanostatic system (Biologic, France), under dark conditions by applying a 5 mV voltage perturbation with the frequency ranging between 1 MHz and 0.1 Hz. The Z-View Analyst software was used to model the Nyquist plots obtained from the impedance measurements.\\n\\nFilm thicknesses were measured using a Veeco Dektak 150 surface profilometer. Time-resolved photoluminescence (TrPL) spectra were obtained on a PL spectrometer (Edinburgh Instruments, FLS 980), excited with a picosecond pulsed diode laser (EPL-375). A Hamamatsu C5680-04 streak camera was used for TrPL. UV-Vis-NIR spectra were obtained using a Shimadzu UV-2550 spectrophotometer. The X-ray diffraction (XRD) patterns were recorded on a Rigaku SmartLab X-ray diffractometer with Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5) at room temperature. The data were collected with a 0.01\\u00b0 step size (2\\u03b8). A field emission scanning electron microscope (Hitachi SU8020) was used to acquire SEM images.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70; 100 >> 135,\\n Perovskite_deposition_thermal_annealing_time: 30.0; 3.0 >> 15.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium isopropoxide (97%), 4-tert-butylpyridine (96%), Li-TFSI (99.95%), acetonitrile (99.8%), dimethylformamide (DMF, 99.8%), and chlorobenzene (99.8%) were purchased from Sigma-Aldrich. PbI2 (99%) was purchased from Acros Organics. Methylammonium iodide (MAI, >98%), was supplied by UniRegion. Spiro-OMeTAD was purchased from Luminescence Technology. 2-propanol (H2O\\u202f<\\u202f0.005%) was purchased from Merck. HCl (37%) was purchased from Fisher Scientific. Fluorine-doped tin oxide (FTO) glass (TEC7, sheet resistance\\u202f=\\u202f8\\u202f\\u03a9/\\u25a1, transmittance\\u202f>\\u202f80%, thickness\\u202f=\\u202f2.2\\u202fmm) was purchased from Pilkington. Alkali-free glass (Eagle XG) was purchased from Corning. Ag (99.99%) was purchased from Gredmann. All chemicals were used as received without further purification.\\n\\n2\\u202fcm\\u202f\\u00d7\\u202f2\\u202fcm FTO substrates were first immersed in an ultrasonic bath with detergent dissolved in deionized (DI) water for 12\\u202fmin and then rinsed using DI water, acetone, and isopropanol. After drying with a nitrogen gun, the FTO substrates were decontaminated by UV-ozone treatment for 15\\u202fmin.\\nTitanium dioxide (TiO2) precursor was prepared by mixing solution-1 that dissolves 184.5\\u202f\\u03bcl of titanium isopropoxide (TTIP) in 1.265\\u202fml of anhydrous 2-propanol and solution-2 that dissolves 17.5\\u202f\\u03bcl of 2-M HCl in 1.265\\u202fml of anhydrous 2-propanol; the mixture was stirred for 30\\u202fmin. Then, 65\\u202f\\u03bcl of TiO2 precursor was spin-coated on the FTO substrate at 2000\\u202frpm for 60\\u202fs. The precursor-coated FTO was then thermally calcined using a furnace at 500\\u202f\\u00b0C for 30\\u202fmin.\\nThe MAPbI3 perovskite absorber and spiro-OMeTAD hole transport layer were consecutively deposited in a nitrogen-filled glove box (mBRAUN, UNIlab-B) with H2O concentration\\u202f<\\u202f0.5\\u202fppm and oxygen concentration\\u202f<\\u202f5\\u202fppm. A one-step method was used for perovskite deposition. Then, 578\\u202fmg of PbI2 and 200\\u202fmg of MAI with molar ratio PbI2:MAI\\u202f=\\u202f1:1 were added to 1\\u202fml of DMF and stirred for one day to form an intermediate phase of MAI-PbI2-DMF. Furthermore, 65\\u202f\\u03bcl of MAI-PbI2-DMF was spin-coated on the TiO2-coated FTO substrate. Next, 200\\u202f\\u03bcl of anhydrous chlorobenzene, which served as an anti-solvent, was dispensed after spinning MAI-PbI2-DMF for 7\\u202fs, and the color of the perovskite film changed from green to brown. Then, the sample was heated at 100\\u202f\\u00b0C for 10\\u202fmin on a hot plate to form perovskite crystals. The perovskite-coated samples were then treated by DBD for 0/5/10/20/40/60\\u202fs. Before DBD treatment, the sample was removed from the hot plate and naturally cooled for 2\\u202fmin.\\nFig. 1 shows the schematic of the DBD setup used in this study. It is a surface DBD system. The powered electrode of the DBD was made of a 3\\u202fcm\\u202f\\u00d7\\u202f3\\u202fcm square copper foil. The ground electrode was a stainless steel mesh with the same dimension as the copper foil. A 1-mm-thick and 4\\u202fcm\\u202f\\u00d7\\u202f4\\u202fcm quartz plate was placed between the two electrodes. A high-voltage (HV) AC generator (PVM12, Information Unlimited), featured with a compact size, was used to supply a sinusoidal AC wave with frequency of \\u223c50\\u202fkHz and amplitude of \\u223c8.5\\u202fkVpp to the copper electrode. The deposition power was \\u223c35\\u202fW. The samples were placed directly on the metal mesh of DBD device with the perovskite layer facing the plasma. The plasma system was filamentary in nature and the filamentary discharge was generated between the stainless steel mesh and the quartz plate. The reactive species formed in the plasma then diffused toward the treated sample surface located on the other side of the mesh. The effect of inhomogeneity caused by the non-uniform nature of the filamentary discharge on the treated surface was therefore greatly minimized. After DBD treatment, spiro-OMeTAD was immediately spin-coated at 2000\\u202frpm for 30\\u202fs to preserve the properties of the DBD-treated perovskites. The spiro-OMeTAD solution was prepared by dissolving 80\\u202fmg of spiro-OMeTAD in 1\\u202fml of chlorobenzene with the addition of 28.8\\u202f\\u03bcl of 4-tert-butylpyridine and 17.5\\u202f\\u03bcl of Li-TFSI solution, and the mixture solution was stirred for 15\\u202fmin; here, the Li-TFSI solution was prepared by dissolving 520\\u202fmg of Li-TFSI in 1\\u202fml of acetonitrile. Next, the samples were stored in a moisture-proof cabinet with relative humidity controlled at 15%\\u201320% for 24\\u202fh for the oxidation of spiro-OMeTAD to proceed. Finally, an 85\\u202fnm-thick Ag layer was deposited by electron-beam evaporation as the contact electrode for PSCs.\\n\\nThe optical emission spectra (OES) of plasma generated in DBD were recorded using a spectrometer (Ocean, FLAME-S-XR1-ES) with a Wi-Fi module (Ocean, STS-KIT-Unice). The Wi-Fi module was used to transmit the recorded spectra from the glove box to the computer. The surface morphology of perovskite films was inspected by scanning electron microcopy (Ultrahigh Resolution FE-SEM, NovaTM, NanoSEM 230) and atomic force microscopy (Asylum Research Cypher S). A high-power X-ray diffractometer (XRD, D8 DISCOVER SSS) was used to examine the crystallinity of the perovskite layers. X-ray photoelectron spectroscopy (Thermo Scientific, Theta Probe) was used for inspecting the chemical bonding status of the perovskite surfaces with/without DBD treatment. The current density-voltage (J-V) characteristics of PSCs were evaluated using a source-meter (Keithley 2400) under the illumination of a solar simulator (Oriel Sol3A) equipped with an AM1.5 filter. Electrochemical impedance spectroscopy (EIS) was used to evaluate the PSCs under illumination in the short-circuit condition with 10\\u202fmV sinusoidal voltage and measurement frequency range of 1\\u2013106\\u202fHz. In XRD analysis, samples with perovskite films coated on Corning Eagle XG glass substrates were used to avoid the interference of FTO and TiO2. For OES, SEM, and AFM analyses, samples with perovskite films deposited on TiO2-coated FTO substrates were used to preserve the authenticity of the conditions of PSCs.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"For deposition of the pristine MAPbI3 films, precursor solutions were prepared with 1.2\\u00a0M PbI2 and 1.2\\u00a0M MAI in the DMF/DMSO co-solvent (VDMF/VDMSO\\u00a0= 9:1). Extra PbI2 with levels of 0%, 2.5%, 5%, and 7.5% (mol\\u00a0%, relative to stoichiometric MAPbI3) was added into the MAPbI3 precursor solutions, respectively, to tune the carrier lifetimes in the MAPbI3 films. For each system, the precursor solutions were stirred at \\u223c25\\u00b0C for 24\\u00a0hr and filtered with a 0.45-\\u03bcm PTFE syringe filter before further use. The MAPbI3 films were then deposited by spin-coating the precursor solution on substrates at 5,000\\u00a0rpm for 30 s. Chlorobenzene (1.5\\u00a0mL) was poured on the surface of the MAPbI3 film \\u223c5\\u00a0s after commencing spin-coating. The as-deposited MAPbI3 films were annealed at 100\\u00b0C for 10\\u00a0min to form the resultant films. For the Cs0.05FA0.80MA0.15PbI2.55Br0.45 (CsFAMA) films, a 1.2\\u00a0M precursor solution was prepared with 0.06\\u00a0M CsI, 0.96\\u00a0M FAI, 0.18\\u00a0M MABr, 1.02\\u00a0M PbI2, and 0.18\\u00a0M PbBr2 dissolved in DMF/DMSO co-solvent (VDMF/VDMSO\\u00a0= 4:1) and 10% extra PbI2 (mol\\u00a0%, relative to CsFAMA) was added to the CsFAMA precursor solution. The precursor solution was stirred at \\u223c25\\u00b0C for 24\\u00a0hr and filtered with a 0.45-\\u03bcm PTFE syringe filter before further use. To obtain the CsFAMA film, we spin-coated the CsFAMA precursor solution on the substrates at 2,000\\u00a0rpm for 10\\u00a0s and 4,000\\u00a0rpm for 20 s, respectively. During the second step, 1.5\\u00a0mL of chlorobenzene was poured on the top surface of the CsFAMA film \\u223c5\\u00a0s before the end of the spin cycle. The as-deposited films were then annealed on a hotplate at 100\\u00b0C for 10\\u00a0min to form the resultant CsFAMA films. All the preparation and deposition steps were performed in a nitrogen-filled glovebox.\\n\\nITO-coated glass substrates (10\\u00a0\\u03a9/sq) were cleaned in soapy water, deionized water, acetone, and isopropanol with sonication. The ITO-coated glass substrates were then subjected to ultraviolet-ozone (UVO) treatment for 10\\u00a0min. For the ETL-free perovskite solar cells, the perovskite films were directly deposited on the ITO substrates according to the procedure mentioned above. Li-doped Spiro-OMeTAD was then spin-coated as the hole-transporting layers on the perovskite films. A solution consisting of 72.5\\u00a0mg of Spiro-OMeTAD, 28.8\\u00a0\\u03bcL of 4-tert-butylpyridine, 17.6\\u00a0\\u03bcL of Li-bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520\\u00a0mg Li-TFSI in 1\\u00a0mL of acetonitrile), and 1\\u00a0mL of chlorobenzene was employed with a spin speed of 3,000\\u00a0rpm for 30 s. To complete the device, Au was thermally evaporated on the hole-transporting layers to serve as the electrode. For the devices with SnO2 ETLs, the SnO2 ETLs were deposited by spin-coating a SnO2 suspension (15 wt % in H2O) in air on the UVO-treated ITO substrates and then annealing on a hotplate at 150\\u00b0C for 20\\u00a0min to form \\u223c20-nm-thick ETLs in air. The glass/ITO/SnO2 substrates were then treated with UVO for 10\\u00a0min. Finally, the perovskite, Li-doped Spiro-OMeTAD and Au layers were sequentially deposited to complete the ETL-containing perovskite solar cells by following the procedures described above for the ETL-free devices.\\n\\nMorphologies of the CsFAMA and MAPbI3 films were imaged with a scanning electron microscope (FEI XL-30 SEM-FEG). AFM images were characterized using a scanning probe microscope (Digital Instruments Dimension 3100). XRD measurements were carried out on a PANalytical Empyrean Powder X-ray diffractometer using Cu K\\u03b1 radiation. The charge-carrier lifetimes were characterized via TRPL experiments using an Edinburgh FLS980 fluorescence spectrometer with excitation wavelength of 510\\u00a0nm. The steady-state PL was also measured with the Edinburgh FLS980 fluorescence spectrometer with excitation wavelength of 510\\u00a0nm. Optical absorption measurements were performed on a Shimadzu UV-3600 spectrophotometer. The EQE was taken using a QE-R instrument from Enlitech without bias voltage. The J-V characteristics and steady-state output were measured using a Keithley 2420 source meter. The illumination source was a Newport Oriel 92192 solar simulator with an AM 1.5G filter, operating at 100 mW cm\\u22122. All devices were masked with area aperture of 0.09\\u00a0cm2 to define the active areas. All the J-V characteristics of perovskite solar cells were evaluated with voltage-scanning speed of 1.0 V/s. A standard silicon solar cell from Newport Corp was used as a reference for J-V and EQE measurements. All measurements were performed under ambient conditions with relative humidity level below 30%.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.80MA0.15PbI2.55,\\n Perovskite_composition_short_form: CsFAMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Prior to coating with the APTES solution, the PET substrate was cleaned by Ar/O2 plasma treatment. 1-wt% APTES solution was prepared by dissolving APTES in methanol. The APTES solution was dropped on the entire PET substrate and then spin-coated at 3000\\u202frpm for 60\\u202fs. The APTES/PET substrate was washed with methanol to remove the residual solvent. Then, the GR sheets grown by chemical vapor deposition were transferred onto the APTES/PET substrates using well-known poly (methyl methacrylate) supporting films.\\n\\nGQDs powder was dispersed in a mixed solvent (deionized water:isopropanol\\u202f=\\u202f1:10) Subsequently, the GQDs solution was added to PCBM by adjusting nG of the resulting PCBM:GQDs to 1, 2.5, and 5\\u202fmg/L, and stirred at room temperature for 12\\u202fh. The ETL solutions of PCBM and PCBM:GQDs were spin-coated at 1500\\u202frpm for 30\\u202fs on the substrates, and annealed at 100\\u202f\\u00b0C for 10\\u202fmin. CH3NH3PbI3 (MAPbI3) solution was prepared by dispersing 1:1-ratio CH3NH3I and PbI2 powder in N,N-dimethylformamide:dimethylsulfoxide mixed solvent (9:1, volume ratio) at 60\\u202f\\u00b0C for 1\\u202fh. The MAPbI3 solution was then spin-coated on the ETL layer by consecutive spin-coatings at 1000 and 5000\\u202frpm for 10 and 20\\u202fs, respectively. During the second spin-coating step, toluene was quickly dropped onto the rotating substrate and subsequently dried at 100\\u202f\\u00b0C for 5\\u202fmin. As a next step, the hole transport layer was prepared on the surface of the MAPbI3 film by spin coating with poly-triarylamine (PTAA) in toluene solution with Li-bis(trifluoromethanesulfonyl) imide (Li-TFSI)/acetonitrile and TBP at 3000\\u202frpm for 30\\u202fs, and then dried in the air. Au counter electrode was then deposited on top of the PTAA layer by thermal evaporation to finalize the solar cell structure.\\n\\nThe size and distribution of GQDs were analyzed using a high-resolution transmission electron microscope (TEM, JEOL JEM-2100F) with electronic energy loss spectroscopy (EELS) mapping capabilities. The topographic images of PCBM:GQDs were obtained in a noncontact mode of atomic force microscope (AFM, Park System XE-100). Cross-sectional structures of the PSCs were observed by field-emission scanning electron microscopy (FE-SEM) (Carl Zeiss, model LEO SUPRA 55). The atomic bonding states of the GR/APTES were studied by Fourier-transform infrared spectroscopy (FTIR, Thermo electron corp Nicolet 5700) and X-ray photoelectron spectroscopy (XPS) using Al ka line of 1486.6\\u202feV. The absorbance/transmittance, sheet resistance (Rs), and work function of the samples were measured by UV\\u2013visible\\u2013near-infrared optical spectrometer (Agilent Varian, model cary 5000), 4 probe van der Pauw method (Dasol eng, model FPP-HS8-40K), and Kelvin probe force microscopy (Park systems, model XE 100), respectively. Here, the calibration of the work function was done by using Au as a reference. The optical properties of the samples were analyzed by steady-state photoluminescence (PL), time-resolved PL (TRPL), and Raman spectroscopy using 325\\u202fnm, 470\\u202fnm, and 532\\u202fnm laser line as the excitation sources, respectively, and the Raman peaks were corrected by the reference Si peaks. Electrochemical impedance spectra (EIS) of the devices were measured using Zive Lab (Wonatech). Current density-voltage (J-V) characteristics were measured at a scan rate of 200\\u202fms/10\\u202fmV by a Keithley 2400 source meter. Photovoltaic parameters of the solar cells were measured by a solar simulator (McScinece K201) under illumination of 1 sun (100\\u202fmW-cm\\u22122, AM 1.5\\u202fG). The active area of the cells was defined as 0.16\\u202fcm2, and the J-V curves were measured at a 0.01\\u202fcm2 active area. External quantum efficiency (EQE) was measured under monochromatic light generated by a Xenon arc-lamp (Oriel Apex Illuminator, Newport) in combination with a monochromator (Cornerstone 260, Newport). Repeated bending stabilities of flexible solar cells were analyzed at a 0.5\\u202fHz bending frequency.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | APTES; Graphene,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.01,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"1-Butanol (99.8%), N, N-Dimethylformamide (DMF, 99.8%), Dimethyl sulfoxide (DMSO, 99.8%), chlorobenzene (99.8%), acetonitrile (99.8%), tert-butyl pyridine (TBP, 96%), bis(trifluoromethane)sulfonamide lithium salt (99.95%) and Titanium diisopropoxide bis(acetylacetonate) (75\\u00a0wt% in isopropanol) were purchased from Sigma-Aldrich. Anhydrous alcohol (99.7%) and 2-propanol (99.7%) were from Sinopharm Chemical Reagent Co.,Ltd. Lead iodide (PbI2, 99.9985%), lead bromide (PbBr2, 99.9%) were purchased from Alfa Aesar Crop. Cesium Iodide (CsI), methylammonium bromide (MABr) and formamidinium iodide (FAI) were purchased from Xi'an Polymer Light Technology Crop, China. The Spiro-OMeTAD was purchased from Luminescence Technology Corp, Taiwan, China. The above agents were used without further purification.\\n\\nNippon Sheet Glass 10\\u00a0\\u03a9/sq was patterned by etching with laser etching machine, cleaned by sonication in 2% Hellmanex water solution for 30\\u00a0min, and rinsed with deionized water, acetone, isopropanol and deionized water for 20\\u00a0min each in an ultrasonic bath, and dried with clean dry air. The substrates were further cleaned with UV ozone treatment for 15\\u00a0min. Then, 60\\u00a0nm TiO2 compact layer was deposited on Fluorine-doped tin oxide-coated (FTO) glass substrate via spin-coated at 2000\\u00a0r.p.m. for 30\\u00a0s using 0.15\\u00a0M titanium diisopropoxide bis (acetylacetonate) in 1-butanol solution followed by heating at 125\\u00a0\\u00b0C for 10\\u00a0min. After the spin-coating, the substrates were annealed at 450\\u00a0\\u00b0C for 30\\u00a0min and cooled down to room temperature. The Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3 precursor solution was prepared according to the Ref , with the addition of the inorganic cesium, the resulting triple cation perovskite compositions are thermally more stable, contain less phase impurities and are less sensitive to processing conditions. Which contains formamidinium iodine (FAI) (1\\u00a0M), PbI2 (1.1\\u00a0M), methylamine bromide (MABr) (0.2\\u00a0M), and PbBr2 (0.2\\u00a0M) in anhydrous DMF:DMSO (4:1, v/v). Then CsI, predissolved as a 1.5\\u00a0M stock solution in DMSO, was added to the mixed perovskite precursor to achieve the desired triple cation composition. The perovskite precursor solution was spin coated in a one-step method at 4000\\u00a0rpm for 15\\u00a0s. Then, the substrate was put into a sample chamber connected to a home-built vacuum-pumping instrumentation. By opening the valve connecting the specimen chamber to the pump system the perovskite film was immediately exposed to low pressure maintained at 30\\u00a0Pa for 10\\u00a0s, followed by full repressurisation by admitting ambient air into the specimen chamber. The effect of annealing temperature (100\\u2013400\\u00a0\\u00b0C) on film morphology was also studied by Minjin Kim et\\u00a0al., different annealing temperatures correspond to different annealing times . Subsequently the substrates were then annealed at 100\\u00a0\\u00b0C for 30\\u00a0min, 200\\u00a0\\u00b0C for 1\\u00a0min, 300\\u00a0\\u00b0C for 8\\u00a0s, and 400\\u00a0\\u00b0C for 4\\u00a0s, respectively. The entire perovskite film fabrication process was performed in the ambient atmosphere with 30% humidity. After perovskite film annealing, the substrates were cooled for 10\\u00a0min, and a hole transfer layer was spin coated at 4000\\u00a0rpm for 30\\u00a0s, which were prepared dissolving 72.3\\u00a0mg spiro-OMeTAD in 1\\u00a0mL chlorobenzene with an additive of 28.8\\u00a0\\u03bcL 4-tert-butyl pyridine and 17.5\\u00a0mL of lithium bis(triuoromethanesulfonyl) imide (Li-TFSI) solution (520\\u00a0mg of LI-TSFI in 1\\u00a0mL of acetonitrile) as hole transport layer on top. Finally, a Au counter electrode (70\\u00a0nm) was deposited by thermal evaporation under high vacuum. All devices were not encapsulated and all the measurements were performed in ambient air with a relative humidity of 50%\\u201360%.\\n\\nCurrent\\u2013voltage characteristics were measured using a Keithley 2420 source-measure unit under AM1.5G illumination at 100\\u00a0mW\\u00a0cm\\u22122 provided by an Oriel Sol 3A solar simulator in ambient environment. Before each measurement, the exact light intensity was determined using a calibrated Si reference diode equipped with an infrared cut-off filter (KG-2, Schott). The devices had an active area of 0.125\\u00a0cm2 without metal mask. The devices were measured by reverse (2.0 v to\\u00a0\\u22120.1 v) and forward (\\u22120.1 v to 2.0 v) voltage scanning at a scan step of about 21.2\\u00a0mV (100 data points in total). The pre-sweep delay time was 40\\u00a0ms, the dwell time at each voltage step was 30\\u00a0ms. Scanning electron microscope (SEM) images were recorded using a high-resolution scanning electron microscope (Hitachi S-8000, Japan). The AFM images were collected by Bruker MultiMode8 test system. An electron beam accelerated to 3\\u00a0kV was used with an in-lens detector. The crystalline structures were examined using X-ray diffraction (XRD, Bruker AXS, D8 Advance) applied with a scanning range of 10\\u201350\\u00b0 and a scanning speed of 2\\u00b0/min. IPCE curves were measured as a function of wavelength from 300 to 800\\u00a0nm using the Newport IPCE system (Newport, USA). The time-resolved photoluminescence spectrum was acquired using the time-correlated singlephoton counting technique (Pico harp 300), and the excitation light pulse was provided using a picosecond diode laser at a wavelength of 760\\u00a0nm with a repetition frequency of 1\\u00a0MHz (PDL 800B).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.7885MA0.1615PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.125,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Well-dispersed perovskite BaSnO3 nanoparticles (BSO NPs) were synthesized by a facile peroxide-precipitate route, as follows: SnCl4\\u00b75H2O (5\\u00a0mmol, 99%, Aladdin), BaCl2\\u00b72H2O (5\\u00a0mmol, 99.5%, Aladdin) and citric acid monohydrate (2.5\\u00a0mmol, 99.5%, Aladdin) were dissolved in hydrogen peroxide aqueous solution (90\\u00a0mL, 30%, Aladdin) with constant string, then ammonia solution (25%, Aladdin) was added in the solution to adjust PH value around 10. After stirring for 12\\u00a0h, the white precipitates were washed by distilled water and ethanol, and were then freeze-dried. The crystallized BSO NPs were obtained by calcining at 800\\u00a0\\u00b0C for 2\\u00a0h in air. Then, BSO NPs and TiO2 (commercial Degussa P25) solution (25\\u00a0mg/mL) were prepared in mixed solvent of n-butanol, methanol and chloroform (14:1:1/v:v:v) with ultrasonic assistance, respectively. A volume of 100\\u00a0\\u03bcL solution was spin-coated on patterned FTO at 1000\\u00a0r.p.m. for 9\\u00a0s and 3000\\u00a0r.p.m. for 30\\u00a0s, then dried at 150\\u00a0\\u00b0C for 10\\u00a0min. These steps were repeated 1, 2, 3, and 4 times to fabricate planar BSO film. Hence, these films were denoted below as BSO-1, BSO-2, BSO-3 and BSO-4, respectively.\\n\\nPerovskite solar cells were fabricated in the following configuration: FTO/BSO-x/CH3NH3PbI3/Spiro-OMeTAD/Ag. CH3NH3I (MAI) was synthesized according to our previous work . The CH3NH3PbI3 (MAPbI3) perovskite film was prepared by a previously reported solvent engineering technology with slight modifications of the deposition parameters. The perovskite solution composed of PbI2 (578\\u00a0mg, 99%, sigma-Aldrich) and synthesized CH3NH3I (200\\u00a0mg) in a mixed solvent (1\\u00a0mL) of DMF and DMSO (9:1/v: v) was stirred overnight at room temperature in Ar-filled glovebox. Prior to use, the perovskite precursor solution was filtered through a 0.22\\u00a0\\u03bcm PTFE syringe filter. The solution was spin-coated on the BSO or TiO2 layer at 4000\\u00a0r.p.m. for 25\\u00a0s and 200\\u00a0\\u03bcL of anhydrous chlorobenzene was quickly dropped onto the center of the rotating substrate before the surface changed to be turbid caused by rapid vaporization of DMF. The obtained films were then annealed at 100\\u00a0\\u00b0C for 10\\u00a0min. A volume of 35\\u00a0\\u03bcL spiro-MeOTAD solution, which composed of 72.3\\u00a0mg spiro-MeOTAD, 28.8\\u00a0\\u03bcL of 4-tert-butyl pyridine and 17.5\\u00a0\\u03bcL of lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520\\u00a0mg/L in acetonitrile) in 1\\u00a0mL of anhydrous chlorobenzene, was spin-coated on the perovskite layer at 4000\\u00a0rpm for 30\\u00a0s. Finally, a 140\\u00a0nm thick Ag electrode was deposited by thermal evaporation to complete the fabrication of the device.\\n\\nX-ray diffraction (XRD) patterns were obtained from a Rigaku D/MAX 2400 diffractometer with Cu K\\u03b1 radiation operating at 35\\u00a0kV and 200\\u00a0mA. The morphology and structure of BSO NPs were characterized a transmission electron microscopy (TEM, JEM-2100F, JEOL). Size distribution of the BSO NPs was characterized by zeta sizer (PerkinElmer, 750S). Scanning electron microscopy (SEM, Hitachi S-4800) operating at 10\\u00a0kV was employed to characterize the morphologies of the films and the cross section of the devices. The Image-Pro Plus software was used to analyze the coverage of BSO NPs on the transparent electrode FTO. The root-mean-square roughness (RMS) and topography images of the perovskite films were measured by atomic force microscopy (AFM, Nanonavi E-Sweep, Seiko) in tapping mode. UV\\u2013vis spectra and transmittance spectrum were recorded on the UV\\u2013vis spectrophotometer (Agilent, model Cary 60). The J-V curves were measured by a Keithley 2400 source meter under AM 1.5G illumination (100\\u00a0mW/cm2). The light intensity was calibrated with an NREL-calibrated Si solar cell with KG-2 filter. A black metal mask with the area of 0.09\\u00a0cm2 was used to prevent scattered light during J-V measurement. The external quantum efficiency spectra were measured on a Enlitech QE-3011 system. Steady-state photoluminescence (PL) spectra were recorded on a luminescence spectrometer (Model: LS 55, Perkin Elmer). Time-resolved photoluminescence (TR-PL) decay spectra were measured on a PTI QM/TM/IM fluorescence spectrometer at room temperature, where poly(methyl methacrylate) (PMMA) serves as protective layer for perovskite films. Impedance spectroscopy (IS) was carried out by using impedance/gain-phase analyzer (Solartron SI 1260) at open-circuit potential condition, with the frequency ranging from 100\\u00a0kHz to 1\\u00a0Hz and modulation amplitude of 10\\u00a0mV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: BaSnO3-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PSC devices with a planar structure consisting of FTO/bl-TiO2/MAPbI3/SWCNT were fabricated to investigate the influence of perovskite morphology on device performance. First, a conductive area was etched into the edge of an FTO glass (12\\u202f\\u03a9/\\u25a1, Solaronix TCO30-8). After cleaning in deionized water and ethanol in an ultrasonic bath, a blocking layer (bl-TiO2) with a thickness of 50\\u202fnm was deposited via nano-cluster deposition (NCD) onto the etched FTO substrate. The NCD technique for an ultrathin, compact TiO2 blocking layer has been described previously [].\\nA smooth and dense perovskite (MAPbI3) film is synthesized using either a one- or a two-step process via CVD. The schematics of the CVD one- and two-step processes are shown in Fig.\\u00a0S1 (Supporting Information).\\nFor one-step deposition, a 2-inch quartz tube furnace (KJMTI OTF1200X) was used with two separate temperature zones. The perovskite materials were simultaneously fabricated by dual-source evaporation from PbI2 and MAI (Sigma Aldrich) with argon as a carrier gas. Then, 300\\u202fmg of MAI and 150\\u202fmg of PbI2 were placed in the upper-flow right zone (zone 1) to confine the vapor. According to the differences in the melting-point temperatures of the PbI2 and MAI powder, the positions of these sources were located at the center and 10\\u202fcm to the right side of zone 1, respectively. The bl-TiO2/FTO substrates were placed in the down-flow on the left side of zone 2 set at temperatures of 60, 80 and 100\\u202f\\u00b0C. The furnace was then sealed and pumped down to a pressure of 1\\u202fTorr under the control of Ar gas flow at 100 sccm.\\nIn the two-step process, a small quartz tube with a 0.5-inch diameter was nested into a larger quartz tube (2-inch diameter). Crucibles containing PbI2 and MAI were separately placed into small and large tube furnaces. First, the temperature in zone 1 was gradually ramped up to 300\\u00b0 C, and then an Ar flow was injected into the small tube at 100 sccm. After 15\\u202fmin, a 180\\u202fnm thickness of PbI2 was used to cover the bl-TiO2/FTO substrate. The second step involved the injecting Ar carrier gas into a large tube support to allow the reaction of MAI and PbI2 conversion to MAPbI3 perovskite. The perovskite layers were optimized for high crystallinity without PbI2 or MAI phases by varying different key parameters such as the gas flow rate, temperature, time, and the amounts of two different sources. After fabrication of the perovskite layer, an in-situ annealing process was performed in the second zone of the furnace immediately after deposition at 100\\u202f\\u00b0C for 60\\u202fmin.\\nFor comparison, the 2-step spin-coating method was also used to prepare perovskite MAPbI3 onto bl-TiO2/FTO substrates. The first spin-coating step involved a 400\\u202fmg/mL PbI2 (Sigma) solution that incorporated N as N-dimethylformamide (DMF) was spin-coated onto the bl-TiO2/FTO then dried at 80\\u202f\\u00b0C for 15\\u202fmin. An MAI solution with a concentration of 40 mg/1 was dropped onto the PbI2-coated bl-TiO2/FTO substrates and let stand for 3\\u20134\\u202fmin to promote the reaction between PbI2 and MAI to form MAPbI3 at room temperature. The samples were spun at 2500\\u202frpm for 25\\u202fs and then annealed under an argon atmosphere at 100\\u00b0 C for 1\\u202fh via RTA (rapid thermal annealing).\\n\\nCounter electrodes were prepared by direct deposition of SWCNTs onto a MAPbI3/bl-TiO2/FTO. This substrate was mounted on the wall of an arc-discharge chamber for in-situ SWCNT deposition. A graphite rod was used as the carbon source. SWCNTs were synthesized under the optimized conditions with an arcing current density of 85 A/cm2 and an atmosphere of 5.3\\u202f\\u00d7\\u202f104\\u202fPa ambient hydrogen for 6\\u202fmin []. The as-deposited SWCNTs had high porosity and a loose structure. The adhesion between the SWCNT network and the substrate was enhanced via chlorobenzene treatment, wherein 10\\u202f\\u03bcl dollops of chlorobenzene were dropped onto the surface of the SWCNT film, which was then heated at 100\\u00b0 C for 10\\u202fmin on a hot plate.\\nFor reference devices, HTM was deposited via the drop-casting of a 10\\u202f\\u03bcl hole-transport solution of spiro-OMeTAD/chlorobenzene (180 mg/1\\u202fmL) with the addition of 50\\u202f\\u03bcL lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI, Sigma)/acetonitrile (170 mg/1\\u202fmL) and 20\\u202f\\u03bcL tert-butylpyridine (tBP, Sigma).\\n\\nOptical transmittances of the SWCNT/glass and the FTO/glass were measured using S-3100 UV\\u2013vis spectroscopy. The resistivity, Hall mobility, and carrier density were measured using a four-point probe method and Hall-effect measurement of the van der Pauw geometry (HL-5500PC, Accent). The crystalline structure and the preferred orientation were characterized by XRD (Rigaku D/MAX-RC) using Cu K\\u03b1 radiation and a nickel filter. The surface morphologies of the perovskite dye and the cross-sectional images of the solar cell devices were analyzed using scanning electron microscopy (SEM) (TOPCON DS-130C). Photocurrent-voltage (I-V) characteristics of the solar cells were measured using an IVIUMSTAT under illumination from a Sun 3000 solar simulator composed of 1000\\u202fW mercury-based Xe arc lamps and AM 1.5-G filters. Light intensity was calibrated with a silicon photodiode. To test stability, we stored the fabricated perovskite devices under an ambient atmosphere that consisted of a white LED lamp with an equivalent intensity of 1 sun. The current-voltage J-V curves of the solar devices were measured daily at the same time and under the same conditions.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: CVD,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: SWCNTs | Spiro-MeOTAD,\\n HTL_additives_compounds: Unknown | Li-TFSI; TBP,\\n HTL_deposition_procedure: Evaporation | Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.25,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The methods for cleaning indium tin oxide (ITO) glass and Poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA) film fabrication can be found elsewhere. The CsPbI3 perovskite films were fabricated by a one-step method, where an equal molar\\u00a0ratio of lead iodide (PbI2) and cesium iodide (CsI) were mixed in DMSO/dimethylformamide (DMF) mixed\\u00a0solvent (v/v, 1/4). Three sulfobetaine zwitterions, 3-(1-pyridinio)-1-propanesulfonate (NDSB201), 3-[2-hydroxyethyl(dimethyl)azaniumyl] propane-1-sulfonate (NDSB211), 3-(decyldimethylammonio) propane-1-sulfonate (SB3-10), were added to the CsPbI3 precursor solution to stabilize the cubic phase of CsPbI3 films. A typical ratio of zwitterion added in CsPbI3 solution was 1.5% (weight ratio of zwitterion to CsPbI3). The zwitterion materials were purchased from Sigma-Aldrich and used as received. The precursor solutions were spin coated on top of PTAA substrates at a spin speed of 4,000\\u00a0rpm. Then the films were annealed at 65\\u00b0C for 5\\u00a0min, followed by annealing at 90\\u2013100\\u00b0C for 20\\u00a0min.\\nXRD of the films was recorded on a BrukerAXS D8 Discover diffractometer. The long-term stability study in Figure\\u00a01E was conducted by storing the samples in dark conditions in air. The air humidity during the 60 testing days varied between 17% and 100%, with a typical humidity level of 30%\\u201340%. Diamond software was used to simulate the XRD pattern of cubic-phase CsPbI3. The lattice constant and space group of CsPbI3 was from previous literature. The samples for XRD measurement in Figure\\u00a02C were measured immediately after fabrication. No thermal annealing was applied to the samples before measurement. The samples were sealed in bottles in an N2 glovebox and then transferred from the glovebox to the XRD equipment to minimize the exposure to air.\\nSEM of the films was recorded on an FEI Helios FIB/SEM 660. The grain size was determined on cross-section SEM images and estimated using Nano Measure software. The grains have an irregular shape. In order to get an accurate size distribution, the size of all the grains was measured in the same lateral direction, and all grains in the SEM images were included in the statistics without selection. The average grain size was derived by fitting the data with Gaussian distribution.\\nFTIR was characterized using a Spectrum Two FTIR (PerkinElmer) with universal attenuated total reflectance (Single Reflection Diamond). The SB3-10 solution for the FTIR measurements in Figure\\u00a02D was prepared by dissolving SB3-10 powder in DMF at 0.1\\u00a0M concentration. Then 0.5\\u00a0M CsPbI3 solution (DMF as solvent) was added to the SB3-10 solution to obtain the desired SB3-10/CsPbI3 ratios.\\nAbsorption spectra and photoluminescence (PL) spectra were recorded on an Evolution 201\\u00a0UV-visible spectrophotometer and iHR320 photoluminescence spectroscopy, respectively. The CsPbI3 precursor solution for UV-visible spectrum measurement in Figure\\u00a02E was prepared by dissolving equal molar concentrations (1 M) of CsI and PbI2 in DMF/DMSO (v/v, 4/1). Then SB3-10 powder was gradually added to the solution to obtain the desired CsPbI3/SB3-10 ratios.\\n\\nThe fabrication of the device was conducted in a glovebox with the oxygen level lower than 100 particles per million. Details about the preparation of the CsPbI3 perovskite precursor solution can be found above. To increase the wetting property of cesium perovskite precursor on PTAA film, the PTAA-coated ITO substrate was pre-wetted by spinning 50\\u00a0\\u03bcL of DMF at 4,000\\u00a0rpm for 5 s. 90\\u00a0\\u03bcL of cesium perovskite precursor was spin coated on PTAA substrate at 2,000\\u00a0rpm for 2\\u00a0s followed by 4,000\\u00a0rpm for 45 s. The sample was drop casted with 90\\u00a0\\u03bcL toluene at 15\\u00a0s after the start of spin coating. CsPbI3 solutions with different concentrations were used to control the thickness of the spun film. CsPbI3 films 200\\u00a0nm, 300\\u00a0nm, 400\\u00a0nm, and 600\\u00a0nm thick were made with 0.4 M, 0.65 M, 0.8 M, and 1.2\\u00a0M solutions, respectively. Lead bromide and lead chloride were used to tune the composition of the perovskite precursor solutions to CsPb(I0.98Br0.02)3 and CsPb(I0.98Cl0.02)3. The spun films were annealed at 90\\u00b0C for 20\\u00a0min. The argon plasma treatment was conducted with a PE-50 plasma cleaning system purchased from Plasma Etch. Typically, the cesium perovskite samples were treated at an operating power of 210\\u00a0W for 2\\u20136\\u00a0s. Then, 2 wt\\u00a0% [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) dissolved in dichlorobenzene was spin coated on perovskite layer at 6,000\\u00a0rpm for 35\\u00a0s and then annealed at 90\\u00b0C for 30\\u00a0min. After deposition of PCBM layers, 25\\u00a0nm C60 was thermally evaporated at a deposition rate of 0.5\\u00a0\\u00c5/s. The devices were finished by the evaporation of 7\\u00a0nm 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and 100\\u00a0nm aluminum or copper electrode. Cooling water was used to cool the samples to room temperature during the deposition of C60, BCP, and electrode. The area of the device was defined as the overlap of ITO with cathode. Slight variation in the area of the device was observed in devices from different batches. Optical microscopy was used to measure the active area accurately; the area typically measured 2.0\\u00a0\\u00d7\\u00a05.0\\u00a0mm.\\n\\nThe J-V curves of the devices were measured in a glovebox. AM 1.5G irradiation (100\\u00a0mW cm\\u22122) with a xenon-lamp-based solar simulator (Oriel 67,005, 150\\u00a0W Solar Simulator) was used as the light source. A Schott visible-color glass-filtered (KG5 color-filtered) Si diode (Hamamatsu S1133) was used to calibrate the light intensity before photocurrent measurements. A Keithley 2400 Source-Meter was used to record the J-V curves. The scanning direction for the J-V measurements was from positive bias to negative bias. The voltage scanning rate was 0.05\\u00a0V s\\u22121. The steady-state photocurrent in Figure\\u00a04D was measured by recording the champion device photocurrent under 0.86\\u00a0V bias. Then the steady-state PCE was obtained by multiplying the measured current by 0.86 V. EQE curves were characterized with a Newport QE measurement kit by focusing a monochromatic beam of light onto the devices.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating | Evaporation,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The ITO/Ag grid/AZO tri-layered electrodes were deposited on glass substrate (20\\u00a0mm\\u00a0\\u00d7\\u00a020\\u00a0mm\\u00a0\\u00d7\\u00a01.1\\u00a0mm) by magnetron sputtering and photoetching at room temperature. The targets used in deposition were an AZO ceramic target (98\\u00a0wt% ZnO\\u00a0+\\u00a02\\u00a0wt% Al2O3), ITO target (90\\u00a0wt% SnO2\\u00a0+\\u00a010\\u00a0wt% In2O3) and Ag target (5\\u00a0N). Prior to deposition, the glass substrates were ultrasonically cleaned in acetone, ethanol and de-ionized water, respectively, for 15\\u00a0min to wipe out the impurities on the surface. Then the bottom ITO or AZO film was deposited at a RF power of 200\\u00a0W and a pressure of 0.4\\u00a0Pa for a constant thickness of 135\\u00a0nm. Subsequently, silver metal grids were constructed by series of sizes with 15\\u00a0\\u00d7\\u00a050\\u00a0\\u03bcm (a grid line width of 15\\u00a0\\u03bcm and grid spacing of 50\\u00a0\\u03bcm), 15\\u00a0\\u00d7\\u00a0125\\u00a0\\u03bcm, 15\\u00a0\\u00d7\\u00a0100\\u00a0\\u03bcm, 10\\u00a0\\u00d7\\u00a0100\\u00a0\\u03bcm and 20\\u00a0\\u00d7\\u00a0100\\u00a0\\u03bcm, to confirm the optimized grid size. The silver layer was deposited by RF magnetron sputtering at 30\\u00a0W under an Ar plasma gas pressure of 0.5\\u00a0Pa. Finally, the top layer was deposited with the same condition as the bottom layer. The fabrication process of the hybrid electrode was schemed in Fig.\\u00a0S1. The whole processes to form the thin films were conducted at room temperature and without post-annealing processing.\\n\\nDifferent structures of AZO/Ag grid/AZO, ITO/Ag grid/AZO and ITO/Ag grid/ITO hybrid electrodes with the optimized silver grid and commercial ITO films were thoroughly cleaned and were treated by an UV-ozone plasma for 3\\u00a0min to increase the hydrophilic nature of the surface. ZnO nanoparticles were synthesized at room temperature by solution processing (See Supplementary) and dispersed in n-butanol and chloroform. The ZnO thin film were deposited by spin-coating dispersed ZnO solution onto the substrates at 3000\\u00a0r.p.m. for 30\\u00a0s and then annealed at 150\\u00a0\\u00b0C for 10\\u00a0min to remove the organic solvent. The procedure was repeated several times to obtain a continuous smooth film with an appropriate thickness. CH3NH3PbI3 (MAPbI3) layer was spin-coated on the ZnO nanoparticle film using a two-step method. First, PbI2 layer was deposited by spin-coating 1\\u00a0M PbI2 solution with the solvent of dimethylformamide (DMF) at 3000\\u00a0r.p.m. for 30\\u00a0s. Next, 50\\u00a0mg/mL CH3NH3I/IPA solution was spin-coated at 3000\\u00a0r.p.m. for 30\\u00a0s on top of PbI2 film, then dried under a flow of clean air at 85\\u00a0\\u00b0C for 10\\u00a0min to form MAPbI3 layer. Subsequently, the spiro-OMeTAD hole transfer layer (72.3\\u00a0mg of spiro-OMeTAD, 28.8\\u00a0\\u03bcL of 4-tert-butyl pyridine and 17.5\\u00a0\\u03bcL lithium-bis (trifluoromethanesulfonyl) imide (Li-TFSI) solution (520\\u00a0mg Li-TFSI in 1\\u00a0mL acetonitrile) all dissolved in 1\\u00a0mL chlorobenzene) was deposited by spin coating at 4000\\u00a0r.p.m. for 30\\u00a0s. Finally, a 120\\u00a0nm thick Au layer was deposited by thermal evaporation. The area of Au electrode was 0.1\\u00a0cm2. Especially, all processes of device fabrications were carried out under an ambient condition.\\n\\nThe electrical properties of the hybrid electrodes were determined by Hall effect measurement system (Nanometrics HL5500 Hall System) and the optical transmittance spectra were obtained by an ultraviolet\\u2013visible diffuse reflection spectroscopy (UV\\u2013vis-DRS, Shimadzu UV-3600). The surface morphologies were obtained by field-emission scanning electron microscopy (FESEM, JEOL 7100F) and atomic force microscope (Ntegra upright, NT-MDT, Russia). A surface profile (Tencor, Alpha-Step D-120) was used to measure the thickness of Ag grid. The X-ray diffraction (XRD) patterns (2\\u03b8 scans) were obtained by Bruker Advanced D8 X-ray diffractometer using Cu K\\u03b1 (\\u03bb\\u00a0=\\u00a00.154\\u00a0nm) radiation. A transmission electron microscope (TEM) (Tecnai G20, FEI) was used to measure the diameter of ZnO nanoparticles. Current density-voltage (J-V) curves of the fabricated perovskite solar cells were measured using Keithley 237 under AM 1.5G one-sun illumination provided by a solar simulator (Newport Oriel Sol 3A Class AAA, 64023A). The incident photo-current conversion efficiency (IPCE) spectrum was measured by CIMPS-2 optical system at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO | Au-grid | AZO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 85,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All of the materials were purchased from Sigma-Aldrich Corp or Alfa Aesar Corp, unless otherwise specified, The Spiro-OMeTAD was purchased from Luminescence Technology Corp, Taiwan, China.\\n\\nThe perovskite precursor solution was prepared in a dry atmosphere in a glove box from 1.0\\u00a0M FAI, 1.1\\u00a0M PbI2, 0.2\\u00a0M MABr and 0.22\\u00a0M PbBr2 in a mixture of DMF, DMSO and NMP (where the volume ratio of DMF/DMSO is 4:1, and the change volume ratio of NMP/DMSO is 0:4, 0.5:4, 1:4, 2:4, 4:4). We note that this composition contains a lead excess as reported elsewhere . Then the 1.5\\u00a0M CsI solution in DMSO was mixed in above solution with the volume ratio of 5:95.\\n\\nThe TiO2 blocking layer was placed onto 0.125\\u00a0cm2 Fluorine-doped tin oxide-coated (FTO) glass substrate (Pilkington, TEC-8, 14\\u03a9 per sq) which was cleaned by UV-ozone treatment for 15\\u00a0min, followed by consecutive cleaning with detergent and ethanol. Preparation of TiO2 blocking layer was as same as previous literature . The mixed perovskite films were prepared by two-step spin-coating (the perovskite precursor solution and chlorobenzene anti-solvent). Perovskite precursor solutions were made by mixing metal halides and amine halides in a predetermined ratio in the NMP-DMSO-DMF mixed solvent. The perovskite solution was deposited on TiO2 blocking layer by a spin-coating method, at 1000\\u00a0rpm and 6500\\u00a0rpm for 10\\u00a0s and 20\\u00a0s, respectively. Chlorobenzene (120\\u00a0\\u03bcL) as anti-solvent was dropped on the substrate during the second step, which must be quickly cast on 5\\u00a0s before the end for the purpose of acquiring uniform and black film. The perovskite need to be annealed at 100\\u00a0\\u00b0C for 1\\u00a0h on the hot plate. A 20\\u00a0\\u03bcL of spiro-OMeTAD solution was spin-coated on the perovskite layer/TiO2 blocking layer/FTO substrate at 4000 rmp for 30\\u00a0s, which was made by dissolving 72.3\\u00a0mg of spiro-OMeTAD in 1\\u00a0mL chlorobenzene with an additive of 28.8\\u00a0\\u03bcL 4-tert-butyl pyridine and 17.5\\u00a0mL of lithium bis(triuoromethanesulfonyl)imide (Li-TFSI) solution (520\\u00a0mg of LI-TSFI in 1\\u00a0mL of acetonitrile) as hole transport layer on top. Finally, 80\\u00a0nm-thick gold electrodes were laid by thermal evaporation using a shadow mask. Thus perovskite solar cells with the structure of FTO/TiO2/perovskite/spiro-OMeTAD/Au were fabricated.\\n\\nFTIR spectra were acquired in the transmission mode using Nicolet iS50 FTIR spectrometer. The morphology and cross-section of the perovskite films were observed by field-emission scanning electron microscopy (SEM, Hitachi S-4800, Japan). The crystalline structures were examined by X-ray diffraction (XRD, Bruker AXS, D8 Advance). The current density-voltage (J-V) curves were measured by a Keithley 2420 source-measure unit under illumination of 100\\u00a0mW\\u00a0cm\\u22122 (AM 1.5G) provided by an Oriel Sol 3A solar simulator in an ambient environment. The light intensity was corrected by using a NREL-calibrated Si solar cell equipped with KG-2 filter. The devices had an active area of 0.125\\u00a0cm2 without the metal mask. Stability of JSC and PCE was measured by Electrochemical workstation (CHI660E, Chenhua Co. Ltd, Shanghai). The devices were measured by reverse (2.0 to\\u00a0\\u22120.1\\u00a0V) and forward (\\u22120.1\\u20132.0\\u00a0V) voltage scanning at about a 21.2\\u00a0mV scan step (100 data points in total). UV\\u2013vis absorption spectra were obtained by using a PerkinElmer Lambda 950UV/VIS/NIR spectrometer. The time-resolved photoluminescence (TRPL) spectrum was acquired using the time-correlated single-photon counting technique (Omni-\\u03bb Monochromator), and the excitation light pulse was provided using a picosecond diode laser at a 775\\u00a0nm wavelength. The roughness of the films was recorded on atomic force microscope (AFM, Multimode-8J, America).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.125,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Anhydrous alcohol (99.7%) was from Sinopharm Chemical Reagent Co, Ltd. Acetonitrile (99.8%), 1-Butanol (99.8%), N, N-Dimethylformamide (DMF, 99.8%), dimethyl sulfoxide (DMSO, 99.8%), chlorobenzene (99.8%), tert-butyl pyridine (TBP, 96%), Nickel phthalocyanine (85%), bis(trifluoromethane) sulfonamide lithium salt (Li-TFSI, 99.95%) and titanium diisopropoxide bis(acetylacetonate) (75\\u202fwt% in isopropanol) were purchased from Sigma-Aldrich. Cesium Iodide (CsI), formamidinium iodide (FAI) and methylammonium bromide (MABr) were purchased from Xi'an Polymer Light Technology Crop, China. Lead iodide (PbI2, 99.9985%) were purchased from Tokyo Chemical Industry. The Spiro-OMeTAD as HTL was purchased from Luminescence Technology Corp, Taiwan, China. All materials were used without further purification unless otherwise stated. All steps were performed under ambient conditions, but the perovskite and hole-transport material solutions were mixed inside an Argon glove box.\\n\\nFluorine-doped tin oxide (FTO)-glass substrates etch into the desired device with a laser etcher prior to cleaning and then cleaned by ultrasonication in Hellmanex (2%, deionized water) for 30\\u202fmin, rinsed thoroughly with acetone, isopropanol, de-ionized water and ethanol (each for 10\\u202fmin), consecutively. Afterwards, the FTO glasses were treated with UV ozone for 30\\u202fmin and plasma cleaning for 5\\u202fmin respectively. To prepare a dense TiO2 electron transport layer, the cleaned FTO glass was coated with a TiO2 solution by a two-step spin-coating method with commercial titanium diisopropoxide bis(acetylacetonate) (75% in 2-propanol, Sigma-Aldrich) diluted in 1-butanol solution (3:40, volume ratio), the first step was 700\\u202frpm for 5\\u202fs with an acceleration of 1000\\u202frpm\\u202fs\\u22121, the second step was 2500 for 15\\u202fs with a ramp-up of 2000\\u202frpm\\u202fs\\u22121. The compact TiO2 coated FTO substrates were dried at 120\\u202f\\u00b0C for 15\\u202fmin and annealed at 550\\u202f\\u00b0C for 30\\u202fmin and then allowed to cool down to room temperature slowly. The thickness of the obtained TiO2 electron transport layer (ETL) is about 50\\u202fnm.\\n\\nA perovskite precursor solution was obtained through using one-step spin-coating procedure. The Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3 precursor solution was prepared containing PbI2 (1.1M), FAI (1.0M), PbBr2 (0.2M) and MABr (0.2M) indimethylsulphoxide/anhydrous dimethylformamide (1:4 (v:v)). Then, CsI, (5% volume, 1.5\\u202fM, pre-dissolved in DMSO as a stock solution) was added to the precursor solution to achieve the desired triple cation composition. The sintered TiO2 substrate was cleaned in a plasma cleaner for 3\\u202fmin before the perovskite precursor was spin-coated. The mixed precursor solution was spin-coated onto the compact TiO2 films in a two-step program at 1000\\u202frpm for 10\\u202fs and 6000\\u202frpm for 20\\u202fs. In the first step, 20\\u202f\\u03bcL perovskite precursor was evenly coated on FTO, and the program was started. The second step, 10\\u202fs before the end of the procedure, 120\\u202f\\u03bcL of anti-solvent were quickly added to the rotating substrate. The substrate was then immediately transferred on a hotplate and heated at 100\\u202f\\u00b0C for 60\\u202fmin. The mixed antisolvent was prepared as follows: Nickel phthalocyanine was added to the pure CB and stirred for 2\\u202fh to prepare different concentrations of mixed anti-solvent (NiPc/CB) (0, 0.05, 0.25, 0.5, 0.75 and 1\\u202fmg\\u202fmL\\u22121). For concise, the above samples were denoted NPC0, NPC0.05, NPC0.25, NPC0.05, NPC0.75 and NPC1, respectively. Prior to use, the mixed anti-solvent was sonicated in an ultrasonic bath for 5\\u201310\\u202fmin to form a uniform green liquid.\\n\\nThe hole-transport layer was subsequently deposited on the top of perovskite film using a spiro-OMeTAD solution (70\\u202fmM in chlorobenzene). Spiro-OMeTAD was prepared using 17.5 \\u03bcL of lithium bis (triuoromethanesulfonyl) imide (Li-TSFI) solution (520\\u202fmg of Li-TSFI in 1\\u202fmL of acetonitrile), 28.8\\u202f\\u03bcL 4-tert-butyl pyridine and 72.3\\u202fmg spiro-OMeTAD in 1\\u202fmL chlorobenzene. The HTL was spin-coated at 4000\\u202frpm for 30\\u202fs with 20\\u202f\\u03bcL of spiro-OMeTAD solution. Finally, Au electrode (approximately 100\\u202fnm thick) was deposited on the top of HTL by thermal evaporation under high vacuum.\\n\\nThe crystallinity and structure of perovskite films were characterized using X-ray diffraction (XRD, Bruker AXS, D8 propulsion) with 2 Theta range from 5\\u00b0 to 80\\u00b0 at a scan rate of 10\\u00b0/min. The field emission scanning electron microscope (Hitachi S-8000, Japan) was utilized to observe the morphology of perovskite and the thickness of each layer of the battery. Intelligent mode atomic force microscopy (AFM) was carried out using a Bruker MM8 instrument to measure the coarseness of the perovskite film surface. The current-voltage (J-V) characteristics of the perovskite devices were measured using a Keithley 2420 source-measure units under AM 1.5G illumination at 100\\u202fmW\\u202fcm\\u22122 provided by an Oriel Sol 3A solar simulator in an ambient environment. The effective area of the cell was defined as 0.125\\u202fcm2 using a shadow mask. Incident-photon-to-current conversion efficiency (IPCE) curves were measured as a function of wavelength from 300 to 800\\u202fnm using the Newport IPCE system (Newport, USA). Optical absorption characteristics of the perovskite film were measured in a Lambda 950 UV/Vis spectrophotometer. Photoluminescence (PL) was used to assess the carrier recombination lifetime. Electrochemical impedance spectroscopy (EIS) testing was conducted on a CIMPS-4 system (Zahner, ZOYPE).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.5I2.5,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.125,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I was synthesized by reacting hydroiodic acid (50 mL, 57% in water, Sigma-Aldrich) and methylamine (50 mL, 40% in methanol, TCI) in a 250 mL round bottom flask at 0 \\u00b0C for 2 h with stirring. The precipitate was recovered by evaporation of solvents at 60 \\u00b0C for 3 h by a rotary evaporator. To purify MAI, the precipitate was dissolved in ethanol and recrystallized from diethyl ether. The recrystallization process was repeated two times and finally dried at room temperature in a vacuum oven for 24 h. MAI(PbI2)1\\u2212X(CuBr2)X solution was prepared by mixing the CH3NH3I powder, PbI2 and CuBr2 (1: 1-X: X mole ratio, where x =0, 0.025, 0.050, 0.075 and 0.100) in \\u0263-butyrolactone (GBL) and DMSO mixed solvent with 7:3 (vol.: vol.) ratio at 70 \\u00b0C for 12 h.\\n\\nFor perovskite planar hybrid solar cells device fabrication, firstly, the patterned ITO glass substrates were cleaned with DI water, acetone and isopropanol and dried in oven at 140 \\u00b0C overnight. After UV-ozone treatment for 15 min, PEDOT:PSS (Clevios AI4083) was spin-coated on ITO glass substrates at 3500 rpm for 60 s and dried at 150 \\u00b0C for 20 min. CH3NH3I(PbI2)1\\u2212X(CuBr2)X perovskite solution was spin coated in glove-box at 4000 rpm for 60 s, followed by a step of 1000 rpm for 20 s. During the 2nd step of 4000 rpm for 60 s, a chlorobenzene (CB) solution (100 \\u00b5L) was dropped on the substrate during spin coating after 40 s and continued the spin for further 20 s. Then, the samples were dried on hot plate at 100 \\u00b0C for 5 min. The PCBM (EM Index) layer was deposited on the ITO/PEDOT:PSS/Perovskite substrate by spin coating PCBM (20 mg/1 mL in CB) solution at 1200 rpm for 60 s. Finally, the LiF/Al (0.5 nm/100 nm) counter electrode was deposited by thermal evaporation.\\n\\nAbsorption spectra of perovskite films on ITO glass substrates were recorded on a Shimadzu UV-2550 spectrophotometer. XRD was performed using a 2 kW Rigaku SmartLab X-ray diffractometer in reflection mode 9 kW (45 kV, 200 mA, Cu, \\u03bb=1.5409 \\u00c5, rotating anode) with scintillation counter detector. FE-SEM was performed on Tescan Mira 3 LMU FEG operated at 20 kV. X-ray photoelectron was performed on AXIS Nova (150 W, monochromatic Al-K\\u03b1, 40 eV). Film thicknesses were measured with a surface profile-meter (KLA Tencor). The UPS measurements were performed with a AXIS \\u2013 NOVA (KRATOS Inc.) instrument at a base pressure of 2.0\\u00d710\\u22129 Torr. The setup was equipped with a helium discharge lamp with excitation energy of 21.22 eV. The XPS data were obtained on a KRATOS AXIS NOVA instrument using 150 W AlK\\u03b1 radiation at a base pressure of 10\\u22129\\u201310\\u22128 Torr. The C-V characteristics were performed by Agilent 4284 A LCR Meter. The sheet resistance of perovskite films were measured by using surface/sheet resistivity measurement system (Hiresta-UP MCP-HT450) using a concentric ring probe technique.\\n\\nThe current density\\u2013voltage (J\\u2013V) curves were measured by a solar simulator (Polaronix\\u00ae K201 Solar Simulator LAB50, McScience) with a source meter (KEITHLEY 2400) under illumination of 1 sun (100 mW/cm2 AM 1.5G) which is calibrated with a Si-reference cell certificated by PV measurements Inc., USA. The EQE was measured by using a K3100 \\u2013 Spectral IPCE measurement system (McScience).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MACu0.05Pb0.95Br0.1I2.9,\\n Perovskite_composition_short_form: MACuPbBrI,\\n Perovskite_additives_compounds: CuBr2,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (CH3NH3I) was purchased from Lumtec (>99.5%). Spiro-OMeTAD was purchased from Jilin OLED Materials Co. Ltd. Lead iodide (PbI2), 4-tert-butylpyridine (tBP), and bis(trifluoromethane)sulfonimide lithium salt (LiTFSi) were purchased from Aldrich. Sol\\u2013gel ZnO solution was prepared by mixing zinc acetate dihydrate (Zn(CH3COO)2\\u00b72H2O, Aldrich, 99.9%, 1.64 g) and ethanolamine (NH2CH2CH2OH, Aldrich, 99.5%, 0.5 g) into 2-methoxyethanol (CH3OCH2CH2OH, Aldrich, 99.8%, 10 g) under vigorous stirring for 30 min at room temperature .\\nPatterned ITO glass substrates (~10 \\u03a9/\\u25a1) were cleaned sequentially by acetone, ethanol, and isopropanol for 20 min each. The substrates were oven-dried at 120 \\u00b0C for 10 min and treated with ultraviolet ozone plasma for 15 min. Subsequently, the sol\\u2013gel ZnO solution was spin-coated onto the ultraviolet ozone\\u2013treated ITO substrate at the speed of 5000 rpm for 40 s and dynamically annealed to 150 \\u00b0C with a ramp rate of ~50 \\u00b0C min\\u22121 and holding time for 20 min under ambient air, resulting in films ~50 nm thick. PbI2 solution in DMF (400 mg mL\\u22121, prepared by stirring at 50 \\u00b0C for 2 h) was spin-casted onto the ZnO layer at 5000 rpm for 40 s and baked at 100 \\u00b0C for 5 min. Next, to form MAPbI3, MAI solution (50 mg mL\\u22121 in IPA) was drop and spin casted at 2500 rpm for 30 s followed by solvent drying at 5000 rpm for 30 s, and was then annealed at 80 \\u00b0C for 10 min. The final thickness of the MAPbI3 was ~250 nm. All processing was done in air with the relative humidity of ~30%; this procedure is modified from a previous report. A hole transport layer comprising 75 mg of Spiro-OMeTAD, 17.5 \\u03bcL of Li-TFSI (520 mg mL\\u22121 of LiTFSI in acetonitrile), and 28.8 \\u03bcL of tBP in 1 mL of chlorobenzene was spin-coated on top of the perovskite film at 3000 rpm for 60 s in a N2 glove box, yielding a film ~200 nm thick. Finally, to form the cathode, 100 nm of Ag was thermally evaporated (~10\\u22126 Torr) onto the hole transport layer. The active area of each PSC was defined by a metal mask as 0.12 cm2. Each device was encapsulated in air by applying Kapton polyimide (PI) tape to the surface of the device. Subsequently, UV-curable photopolymer (NOA 63, Norland Products Inc.) was dropped onto the PI tape with a slide glass and cured by UV light (LIT-2000, NEXTRON) for 15 min\\n\\nCross-sectional FESEM images of PSC devices were acquired using a Hitachi S-4800 FESEM instrument. XRD measurements were carried out using a PANalytical Empyrean equipped with a Phoenix Oxford LTK temperature controller; the sample was cooled by liquid helium in a low-pressure chamber of 5\\u00d710\\u22125 Torr. PL measurements were performed using LabRAM HR UV/Vis/NIR-PL (Micro-PL) instrument equipped with a 514 nm laser source and a Lincoln TMS 94 temperature controller; the sample was placed for measurement in a closed-cycle He cryostat chamber. The fabricated PSC devices were measured under simulated AM1.5 G illumination of irradiance 100 mW cm\\u22122 (Oriel Sol 1 A, Newport) and J\\u2013V curves were measured using a Keithley 2400 SMU. To accurately define the active area, a shadow mask with an exposed area of 0.12 cm2 was employed during the J\\u2013V measurements. The quantum efficiency measurement system (Oriel IQE-200) used to acquire IPCE spectra consisted of a 250 W quartz tungsten halogen lamp as the light source, a monochromator, an optical chopper, a lock-in amplifier, and a calibrated silicon photodetector. For lower temperature conditions, digital-controller thermoelectric equipment was used as a temperature controller, and the device was placed into a chamber under a continuous flow of nitrogen gas. At low temperature, the cells were allowed to equilibrate at each temperature in the dark for 10 min prior to J\\u2013V measurements.\\nTransient chronoamperometry measurements were carried out using a potentiostat/galvanostat (Ivium CompactStat). The photo-CELIV setup consisted of a diode-pumped solid-state laser (CNI laser, MBL-FN-473), a function generator (Tektronix, AFG3022C), and an oscilloscope (Budget, 300 MHz with 50 \\u03a9 input). A blue laser of wavelength 473 nm was used as an excitation source with the pulse energy of <0.05 \\u00b5J cm\\u20132 and pulse width of ~30 \\u00b5s (microsecond photo-CELIV). The laser power was measured using an optical power meter (Newport model 1835 C), and both the voltage ramp (triangular voltage) and the delay time (t delay) between the laser and applied voltage ramp were synchronized by a function generator. Photo-CELIV signals were recorded by a storage oscilloscope using a 50 \\u03a9 load resistance; the conditions of ~1 \\u03bcs t delay and 0.96 V offset voltage were fixed for all devices. For transient photocurrent measurements, the device was illuminated under irradiance of 100 mW cm\\u22122 AM1.5G and a blue laser (CNI laser, MBL-FN-473); the device was kept in a short-circuit condition and the photocurrent signal was recorded by the oscilloscope.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 80.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"In a flame dried Schlenk tube equipped with a stir bar phthalonitrile (1, 2 or 3, 1 mmol) and Zn(OAc)2\\u00b72H2O (55 mg, 0.25 mmol) were suspended in 1-pentanol (2 ml). The mixture was stirred for 15 min under a nitrogen atmosphere then DBU (150 \\u00b5L, 1 mmol) was added and the mixture was heated at 145 \\u00b0C for further 24 h. After cooling to room temperature the reaction mixture was poured into MeOH and the solid was collected by filtration on a B\\u00fcchner funnel. The solid was thoroughly washed with MeOH, dried under reduced pressure. Column chromatography (silica gel, THF) followed by repeated washing with cold pentane gave the desired ZnPc as a mixture of positional isomers.\\n\\nFTO glass (NSG) was sequentially cleaned using detergent, acetone, and ethanol by ultrasonic bath for each 20 min. And then 40 nm TiO2 blocking layer was deposited on the heated FTO at 450 \\u00b0C by spray pyrolysis, using a precursor solution of 0.6 ml of titanium diisopropoxide and 0.4 ml of bis(acetylacetonate) in 9 ml of anhydrous isopropanol. About 250 nm mesoporous TiO2 was spin-coated on the surface of bl-TiO2/FTO substrate at a speed of 2000 rpm for 20 s from diluted 30NRT (Dyesol) with ethanol (1 g/7 ml). The substrate was then sintered at 500 \\u00b0C for 20 min in air. The MAPbI3 was spin-coated onto the TiO2 mesoporous layer. The precursor solution was prepared as 1.2 M. The spin-coating was going through a two-step; first step is at 1000 for 10 s and then at 5000 rpm for 30 s. In the second step, 100 ml of chlorobenzene was dropped on the spinning substrate at 20 s. The substrates were then annealed at 100 \\u00b0C for 30 min. The HTM solutions were prepared in chlorobenzene. The concentration of BI25, BL07, and BL08 solutions are 50, 30, and 30 mM, respectively and three additives, bis(trifluoromethylsulfonyl)-imide lithium salt (Li-TFSI, Sigma Aldrich), 4-tert-butylpyridine (TBP, Sigma Aldrich), and tris(2-(1H-pyrazol-1-yl)\\u22124-tert-butylpyridine)\\u2013cobalt(III)tris(bis(trifluoromethylsulfonyl)imide) (FK209, Dyenamo), were added at a molar ratio of 0.4, 2.2, and 0.04, respectively. These HTM solutions were spun at 4000 rpm for 30 s. Finally, 80 nm of gold layer was deposited by thermal evaporation.\\nA HR-SEM (ZEISS Merlin) was used to characterize the structure of the device cross-section. Solar cell efficiencies were measured using a potentiostat (Keithley model 2400) under simulated one sun irradiation from a Xe arc lamp with an AM 1.5 global filter. The light intensity was measured by an NREL certified KG5 filtered Si reference diode and was used for calibration. The active area exposed are defined to 0.16 cm2. For IPCE characterization, a 100 W Xe lamp linked to a monochromator (Newport, IQE-200B) to tune the light beam accordingly.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: BI25,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials were purchased from Sigma-Aldrich and used as received without further purification. A perovskite precursor solution could be obtained through the mixture of CH3NH3I and PbI2 (1:1, molar ratio) in the solvent of \\u03b3-butyrolactone and DMSO (7:3, v:v). The TiO2 solution was prepared as an ETM according to the previous method . The spiro-OMeTAD, P3HT, or PTB7 was used for a HTM. A solution containing 28 \\u03bcL of 4-tert-butyl pyridine and 17 \\u03bcL of Li-TFSI (520 mg Li-TFSI in 1 ml acetonitrile) was added to a CB solution (1 ml) of spiro-OMeTAD (80 mg), P3HT(15 mg), or PTB7 (10 mg), respectively. The device structure was ITO/TiO2/MAPbI3/HTM/Au . Regarding the typical device fabrication, ITO glass substrates (15 mm \\u00d7 15 mm, 15 \\u03a9 sq\\u22121 resistance) were first cleaned with decontamination powder and then ultrasonicated successively in DI water, acetone, and anhydrous ethanol (each for 10 min). The ITO glasses were then treated with UV ozone for 15 min. To make compact TiO2 layers, the cleaned ITO glasses were coated with a TiO2 solution by spin-coating at 4000 rpm for 60 s. The compact TiO2 coated ITO substrates were dried at 150 \\u00b0C for 10 min and then allowed to cool down to room temperature slowly. A perovskite precursor solution was spin-coated onto TiO2 layer at 3000 rpm for 40 s with a dripping CB solvent (CB-treated method) or a CB solvent containing HTM with different concentration (e.g., 0\\u20134 mg/ml) (CB/HTM-treated method). The substrates were then heated at 100 \\u00b0C for 10 min and allowed to cool down to room temperature. Subsequently, a HTM was deposited on the top of the CH3NH3PbI3 perovskite layer by spin coating. Devices were then kept overnight in air. Finally, a top Au electrode (100 nm thick) was thermally evaporated on the top of the HTM.\\n\\nJ\\u2013V characteristics of devices were measured under AM 1.5G illumination (100 mW cm\\u22122) from a solar simulator. The morphologies of the conventional device and the layer-evolved device without top Au electrodes were characterized by a field-emission scanning electron microscope (SEM, FEI 450). The X-ray diffraction patterns (XRD) were collected using a PANalytical X\\u2032Pert XRD system with reference X-ray illumination as Cu K\\u03b1 radiation at 0.154 nm. The film absorption spectrum was obtained using a UV\\u2013Vis\\u2013NIR spectrophotometer (Lambda 35, Perkin-Elmer). Photoluminescence (PL) of the films were performed using a fluorescence spectrometer (FLS 980) with an excitation at 470 nm, similar to the one reported previously .\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The fluorine-doped tin oxide (FTO) conducting glass substrates (NSG, 7\\u202f\\u03a9/square) were cleaned sequentially by ultrasonication in detergent, deionized water, acetone, ethyl alcohol and isopropyl alcohol for 30\\u202fmin, respectively. Subsequently, the substrates dried by clean N2 were exposed to UV-ozone for 30\\u202fmin to remove residual organic materials attached to the FTO surfaces. After that, the FTO substrates were immersed into 0.06\\u202fM (3-Aminopropyl) triethoxysilane (APTS) in methyl alcohol and maintained at 40\\u202f\\u00b0C for 180\\u202fmin and then washed by using clear methyl alcohol. To prepare the reaction solution, 2401\\u202fmg citric acid and 751\\u202fmg thioacetamide were added slowly in 0.025\\u202fM indium (\\u2172) chloride solution with 100\\u202fml deionized water under stirring. The FTO substrates were vertically soaked in the reaction solution. Then, the beakers were sealed and kept at 70\\u202f\\u00b0C for 55, 70, 85 and 100\\u202fmin in a water bath kettle, respectively. After the reaction, the In2S3 ETLs grown on FTO substrates were in ultrasonic with deionized water to obtain a clean films and then washed with deionized water and ethyl alcohol in turn and dried by clean N2. To prepare the TiO2 ETL, a TiO2 compact layer was spin-coated on the FTO substrate at 2000\\u202frpm for 50\\u202fs using 0.30\\u202fM titanium diisopropoxidebis (acetylacetonate) in 1-butanol solution, followed by heated at 125\\u202f\\u00b0C for 10\\u202fmin. After cooling to room temperature, the mesoporous TiO2 film was prepared by spin-coating a mixture of 18 NR-T TiO2 paste and anhydrous ethanol 1:7 (w/w) at 3000\\u202frpm for 15\\u202fs, and then sintered at 500\\u202f\\u00b0C for 30\\u202fmin in air. After finishing all procedures, total samples were transferred to a glove box for further processing.\\n\\nThe CsPbIBr2 films were deposited on ETLs using one-step method. The PbBr2 and CsI were purchased from Xi\\u2019an Polymer Light Technology Corp. in China. The perovskite precursor solution was prepared by adding 440\\u202fmg PbBr2 and 312\\u202fmg CsI into 1\\u202fml DMSO and then stirred at 60\\u202f\\u00b0C until completely dissolved in a glove box. The CsPbIBr2 film was deposited on ETLs by spin-coating at 3000\\u202frpm for 45\\u202fs. Subsequently, the as-prepared thin film was kept 55\\u202fs in the petri dish and annealed at 30\\u202f\\u00b0C for 10\\u202fmin and then 160\\u202f\\u00b0C for 20\\u202fmin to improve the crystallization quantity of perovskite thin films. To complete the devices, the organic hole-transporting material (HTM) was deposited on as-prepared CsPbIBr2 films by spin-coating of a mixture solution at 4000\\u202frpm for 40\\u202fs after the films cooling down to the room temperature. The spiroOMeTAD solution was prepared by adding 90\\u202fmg of 2,2\\u2032,7,-7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9\\u2032-spirobifluorene (spiroOMeTAD), 10\\u202f\\u03bcL 4-tert-butylpyridine (TBP), 45\\u202f\\u03bcL of a stock solution consisting of 170\\u202fmg/ml lithium bis(trifluoromethylsulphonyl)imide (Li-TFSI) in acetonitrile and 75\\u202f\\u03bcL of a stock solution consisting of 100\\u202fmg/ml tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)-cobalt(III) Tris(bis-(trifluoromethylsulphonyl)imide)) in acetonitrile to 1\\u202fml chlorobenzene. Finally, 100\\u202fnm Ag was subsequently deposited on hole-transporting layers by thermal evaporation. The active area of all the cells was 0.11\\u202fcm2.\\n\\nThe X-ray Diffraction (XRD) patterns of prepared films were performed by a PANalytical Empyrean diffractometer equipped with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.5406\\u202f\\u00c5). The top-down morphology and structure of prepared films and cross-sectional images of devices were achieved by JEOL JSM-7800F field emission scanning electron microscopy (FESEM). Optical transmittance and absorption of prepared films were measured by Shimadzu UV-1800 UV\\u2013Vis spectrophotometer. The X-ray photoelectron spectroscopy (XPS) was obtained by axis Ultra DLD X-ray photoelectron spectrometer. The Incident Photon-to-Current Efficiency (IPCE) was measured using a Newport-74125 system (Newport Instruments). The room temperature steady-state photoluminescence (PL) spectra was collected by a fluorescence spectrophotometer (Cary Eclipse, Agilent) with an excitation wavelength of 360\\u202fnm. Electrochemical impedance spectra (EIS) was obtained with electrochemical workstation in the dark at positive bias voltages at 0.8\\u202fV in the frequency range of 1\\u202fM to 10\\u202fHz. The photocurrent-voltage (J-V) curves of devices were recorded by an AM 1.5\\u202fG solar simulator (Newport, 2612\\u202fA) that was calibrated by a silicon reference cell to obtain a light intensity of 100\\u202fmW/cm2. The voltage step and dwell time were 10\\u202fmV and 30\\u202fms, respectively. The reverse scan started from 1.2\\u202fV to \\u22120.1\\u202fV, while the forward scan started from -0.1\\u20131.2\\u202fV. Both scan rates were 100\\u202fms/V. The PCE measurements of devices were in air with relative humidity of ~52% and ambient temperature of ~32.5\\u202f\\u2103.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: CsPbBr2I,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 30; 160,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 20.0; 0.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fig.\\u00a01 a displays the architecture of the fabricated perovskite devices: ITO/PC71BM or PC61BM/CH3NH3PbI3 perovskite/Spiro-OMeTAD/MoO3/Ag. Patterned ITO glass substrates (12\\u00a0mm\\u00a0\\u00d7\\u00a012\\u00a0mm, Lumtec) were cleaned sequentially via ultrasonication in soapy DI water, DI water, acetone and isopropanol, each for 10\\u00a0min. [6,6]-phenyl C71 butyric acid methyl ester (PC71BM) and phenyl-C61-butyric acid methyl ester (PC61BM) (1- Material, Inc., concentration: 20\\u00a0mg/mL) were dissolved in chlorobenzene and spin-coated on top of the ITO coated glasses at 1000\\u00a0rpm for 60\\u00a0s. 460\\u00a0mg lead iodide (PbI2) and 159\\u00a0mg methyl ammonium iodide (CH3NH3I or MAI) were dissolved in 1\\u00a0mL DMF (N, N\\u2013dimethylformamide) at 70\\u00a0\\u00b0C overnight in a N2 filled glovebox. The MAPbI3 solution was spin-cast on the PC71BM and PC61BM layers at 2500\\u00a0rpm. Later, the substrates were annealed at 100\\u00a0\\u00b0C for 10\\u00a0min. For HTL, 72.3\\u00a0mg/mL Spiro-OMeTAD (2,2\\u2032,7,7\\u2032-Tetrakis (N,N-di-p- methoxyphenylamino)-9,9\\u2032-spirobifluorene) was doped with 17.5\\u00a0\\u03bcl Li-TFSI (520\\u00a0mg/mL in acetronitrile) and 28.8\\u00a0\\u03bcL 4-TBP in chlorobenzene. The Spiro-OMeTAD layer was spin coated dynamically on the perovskite layer with 2500\\u00a0rpm for 40\\u00a0s in order to prevent the fullerene layer from damage since both layers can dissolve in chlorobenzene. To ensure better hole transport, an additional layer of thin MoO3 film (6.5\\u00a0nm) was deposited on top of the Spiro-OMeTAD layer via thermal evaporation. Finally, 100\\u00a0nm Ag layer was deposited on the Spiro-OMeTAD/MoO3 HTL layer by thermal evaporation with an evaporation rate of 2.5\\u00a0\\u00c5/s under a vacuum condition of 1\\u00d7106 mBar.\\n\\nThe current density\\u2013voltage (J\\u2013V) measurements were performed using a solar cell I\\u2013V testing system from PV Measurements, Inc. (using a Keithley 2400 source meter) under illumination power of 100\\u00a0mW/cm2 by an AM 1.5G solar simulator. The device area was fixed to be 0.12\\u00a0cm2 with the use of a metal shadow mask. UV\\u2013VIS\\u2013NIR spectrometer (Perkin Elmer \\u2013 Lambda 950) was used to measure the transmission and absorption of various layers. The contact angles of PC71BM and PC61BM layers were measured by a Ram\\u00e9-Hart 200-F1 goniometer employing 8\\u00a0\\u03bcL of DMF solvent. The contact angles were registered by a NET-GmbH 1354 digital camera and measured using the DROPimage standard software (version 2.1.3). Perovskite surface topology image was captured by FEI Nova NanoSEM 230 FE-SEM and surface roughness was extracted from atomic force microscopy (AFM) images by Bruker Dimension ICON SPM. X-ray diffraction (XRD) with Cu K\\u03b1 radiation was performed at an angle ranging from 20\\u00b0 to 60\\u00b0 by step-scanning with a step size of 0.02\\u00b0. The impedance and Mott-Schottky measurements were performed with an Autolab PGSTAT-30 equipped with a frequency analyser module in the frequency range of 106\\u20131\\u00a0Hz. AC oscillating amplitude was as low as 20\\u00a0mV (rms) to maintain the linearity of the response.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-70,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD | MoO3,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating | Evaporation,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbI2 and MAI were purchased from Yingkou Optimal Choice Trade, China. [6,6]-phenyl-C61-butyric acid methyl (PC61BM) was purchased from American Dye Source. The bis-functional of C70 (C70-bis) was purchased from 1-Material, Canada. DMF was purchased from Aldrich company. IPA was purchased from Beijing Chemical Factory, China. The materials were used without further purification.\\n\\nDuring the solvent vapor annealing process, the PbI2 film was placed into a glass tube which contained IPA at bottom. Stable vapor gradient along the tube could be acquired after 10\\u00a0min because liquid solvent location was fixed. The vapor pressure of sample was P\\u00a0=\\u00a00.54 (25\\u00a0\\u00b0C) (The length of tube is 3\\u00a0cm and the liquid height is 0.2\\u00a0cm. The solvent vapor pressure P is given by P\\u00a0=\\u00a0L/L0, where L is the distance from the up edge of the setup to the specimen position and L0 is the length given by distance from the up edge of the setup to the surface of the solvent at the bottom of the tube).\\n\\nThe devices were fabricated in the configuration of indium tin oxide (ITO)/Poly (ethylenedioxythiophene): poly (styrenesulfonate) (PEDOT:PSS, Baytron P4083)/CH3NH3PbI3/PC61BM/C70-bis/Al. The ITO glass substrates were cleaned sequentially with detergent and deionized water, acetone, and IPA under sonication for 10min and dried by dry N2. Subsequently, substrates were treated with UV-ozone for 25\\u00a0min. PEDOT:PSS filtered through a 0.45\\u00a0\\u03bcm nylon filter was first spin-coated at 5k rpm for 40\\u00a0s on this well-cleaned ITO glass and dried at 140\\u00a0\\u00b0C in vacuum for 30\\u00a0min. The substrates were transferred into a N2-filled glovebox, where the PbI2 layers were spin-coated from a homogeneous 1\\u00a0mol/L PbI2 75\\u00a0\\u00b0C solution at 4k rpm for 40\\u00a0s on substrates (about 63\\u00a0\\u00b0C) and then immersed in MAI solution (20\\u00a0mg/ml), subsequently annealed at 100\\u00a0\\u00b0C for 2\\u00a0h. Afterward, the PC61BM (15\\u00a0mg/mL in chloroform) and C70-bis surfactant (2\\u00a0mg/mL in IPA) were then sequentially deposited by spin coating at 3k rpm for 60\\u00a0s, respectively. Finally, a layer structure of Al (90\\u00a0nm) was deposited at top of the active layer by thermal evaporation in a vacuum of 2\\u00a0\\u00d7\\u00a010\\u22124\\u00a0Pa to complete the device fabrication.\\n\\nThe morphology of hybrid perovskite films was acquired by field-emission scanning electron microscopy (FESEM) using a Micro FEI Philips XL-30-ESEMFEG microscope at an accelerating voltage of 20\\u00a0kV. The samples were sputter coated with gold before SEM observation.\\nThe crystallinity of perovkite film was analyzed using out-of-plane grazing incidence X-ray diffraction (GIXD) measurements, two-dimentional GIXD (2D GIXD). The GIXD profiles were obtained by using a Bruker D8 Discover reflector with an X-ray generation power of 40\\u00a0kV tube voltage and 40\\u00a0mA tube current. The measurements were achieved in a scanning interval of 2\\u03b8 between 3 and 60\\u00b0. The 2D GIXD profiles were obtained by using BL14B1 at Shanghai Synchrontron Radiation Facility (SSRF; \\u03bb\\u00a0=\\u00a00.124\\u00a0nm).\\nThe photon absorption of active layer and situ absorption spectrum were recorded by UV\\u2013vis absorption spectroscopy (AvaLight-Hal) with halogen lamp source.\\nCurrent density-voltage (I-V) characteristics of the PV cells were measured using a computer controlled Keithley 236 source meter under AM1.5G illumination from a calibrated solar simulator with irradiation intensity of 100\\u00a0mW/cm2. The device area was 12\\u00a0mm2, determined by the overlap of the cathode and anode. An aperture size of 10.6 was used to define the light absorption area, which would avoid the overestimation of the photocurrent density by the optical pining effect .\\nThe external quantum efficiency (EQE) measurement was performed on the QE-R3011 system from Enli Technology Co. Ltd (Taiwan).\\nNanosecond fluorescence lifetime experiments were performed using the time correlated single-photon counting (TCSPC) system under right-angle sample geometry. A 400\\u00a0nm\\u00a0picosecond diode laser (Edinburgh Instruments EPL375, repetition rate 20\\u00a0MHz) was used to excite the samples. The fluorescence was collected by a photomultiplier tube (Hamamatsu H5783p) connected to a TCSPC board (Becker & Hickl SPC-130). The time constant of the instrument response function (IRF) is about 220 ps.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | bis-C70,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Unknown,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 20.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.106,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the solvents used in the experiments were bought from Sigma Aldrich (USA). ITO glass slides with sheet resistance of \\u223c10\\u00a0\\u03a9/sq were bought from CSG Holding Co., Ltd. (China). The AuAg ANCs were synthesized according to the literature by a simple, Fe2+-assisted, citrate co-reduction method in a one-pot reaction manner . PbCl2 (99.999%) and PC61BM were purchased from Alfa Aesar (USA) and American Dye Source, Inc. (Canada), respectively. 1, 8-diiodooctane (DIO) was acquired from TCI Development Co., Ltd. (Shanghai).\\n\\nThe synthesis of methylammonium iodide (MAI) was referred to a previous literature . The MAI was synthesized by mixing hydroiodic acid (57\\u00a0wt%, in water) (20\\u00a0mL) and methylamine (33\\u00a0wt%, in ethanol) (15\\u00a0mL) at 0\\u00a0\\u00b0C for 2\\u00a0h. The crude product was obtained by reduced pressure distillation, and then the product was recrystallized by dissolving in anhydrous ethanol and precipitating in anhydrous diethyl ether for 3 times, and dried at 50\\u00a0\\u00b0C for 24\\u00a0h in vacuum drying oven. The MAPbI3-xClx precursor (40\\u00a0wt%) was prepared by mixing PbCl2 and MAI in a 1:3\\u00a0M ratio in anhydrous N,N-dimethylformamide (DMF, 99.8%) and stirred at 60\\u00a0\\u00b0C. After \\u223c30\\u00a0min, 1\\u00a0wt% of DIO was added to the MAPbI3-xClx precursor, and then the solution was stirred overnight in a nitrogen atmosphere. The precursor was filtered through a 0.45\\u00a0\\u03bcm polytetrafluoroethylene (PTFF) filter before use.\\n\\nITO glass slides were cleaned by ultrasonification in detergent, water, acetone, ethanol and isopropyl alcohol for 15\\u00a0min each time. After being dried, the cleaned ITO substrates were treated with ultraviolet ozone for 20\\u00a0min to make a hydrophilic surface. The ratio of nanocrystals to the PEDOT:PSS (Clevios P VP AI 4083) could be adjusted by the different contents of AuAg ANCs in the solution and the solution were filtrated with a 0.45\\u00a0\\u03bcm filter before use. For comparison, a PEDOT:PSS solution without AuAg ANCs was also been prepared. The films were obtained by spin-coating on the ITO substrates at 5000\\u00a0rpm for 40s and annealing at 150\\u00a0\\u00b0C for 15\\u00a0min in air. Sequentially, the perovskite precursor was coated atop HTL at 3000\\u00a0rpm for 50\\u00a0s in glove box. The perovskite film was thermally annealed at 95\\u00a0\\u00b0C for 80\\u00a0min. 15\\u00a0mg/mL PC61BM in chloroform was spin-coated at 1200\\u00a0rpm for 60\\u00a0s atop the perovskite layer. At last, LiF (1\\u00a0nm) and Al (80\\u00a0nm) were deposited under vacuum at 1\\u00a0\\u00d7\\u00a010\\u22126\\u00a0Torr and a shadow mask was applied to define the active area.\\n\\nThe morphology of AuAg ANCs was obtained by the transmission electron microscopy (TEM, JEOL JEM-2100F, Japan) at an acceleration voltage of 200\\u00a0kV. Absorption and transmittance spectra were measured on a Cary 5000 instrument (Agilent, USA). The configuration of device was obtained by scanning electron microscopy (SEM, S-4700, Hitachi, Japan). The surface morphologies were recorded by atomic force microscopy (AFM, Bruker USA). The thickness of the PEDOT:PSS layer without and with AuAg ANCs was measured by a spectroscopic ellipsometer (M-2000 V, J.A. Woollam Co., USA). The current density-voltage (J-V) curves were recorded on a Keithley 2400 source meter unite under simulated air mass 1.5 global (AM 1.5G) solar irradiation at 100\\u00a0mW/cm2 (SAN_EI ELECTRIC, XEC-300M2, Japan). The incident photon-to-current efficiency (IPCE) was collected on a QE-R3011 system (Enli Technology Co., Ltd., China) in air. Both the illumination intensities of the light sources were calibrated by a standard silicon solar cell for reference. The characterizations of the alternating current impedance spectroscopy (ACIS) were acquired by IM6 electrochemical workstation (Zahner Zennium, Germany) with a bias voltage near the respective V oc in the dark condition. The effective area of the cell was 0.1842\\u00a0cm2. The impedance spectra parameters were analyzed by Z-view software. The measurements of steady-state photoluminescence (PL) were conducted on FLS980 (Edinburgh Instrument, UK). Time-resolved PL spectra were recorded on LifeSpec (Edinburgh instrument, UK) by exciting with a 477 nm laser (5\\u00a0MHz).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl; DIO,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 95,\\n Perovskite_deposition_thermal_annealing_time: 80,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1842,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned ITO glass substrates (12\\u202fmm\\u202f\\u00d7\\u202f12\\u202fmm), from Lumtec, were cleaned via ultrasonication in soapy DI water, DI water, acetone and isopropanol, sequentially, each for 10\\u202fmin. PC71BM (1- Material, Inc.) was dissolved in chlorobenzene to make a 20\\u202fmg/mL solution and spin-coated on top of the ITO coated glass substrates at 1000\\u202frpm for 60\\u202fs to deposit a 53\\u202f\\u00b1\\u202f3.3\\u202fnm film. The deposited film was annealed at 80\\u202f\\u00b0C for 5\\u202fmin.\\n460\\u202fmg lead iodide (PbI2) and 159\\u202fmg methyl ammonium iodide (CH3NH3I or MAI) (1:1\\u202fM ratio) were dissolved in different volumes of DMF (N, N\\u2013dimethylformamide) to make 40, 25 and 18\\u202fwt. % solutions. The solutions were stirred vigorously overnight at room temperature in a N2 filled glovebox. The MAPbI3 solutions, with different wt. %, were spin-cast on the PC71BM layer at different spin speeds (ranging from 2500 to 5000\\u202frpm) to achieve different perovskite layer thicknesses. Later, the substrates were annealed at 100\\u202f\\u00b0C for 10\\u202fmin.\\nSpiro-OMeTAD HTL was spin-coated on top of the perovskite layer in a process reported in our earlier work []. In brief, 72.3\\u202fmg Spiro-OMeTAD (2,2\\u2032,7,7\\u2032-Tetrakis (N,N-di-p- methoxyphenylamino)-9,9\\u2032-spirobifluorene) was dissolved in 1\\u202fmL chlorobenzene and doped with 17.5\\u202f\\u03bcl Li-TFSI (520\\u202fmg/mL in acetronitrile) and 28.8\\u202f\\u03bcL 4-TBP in chlorobenzene. The solution was spin coated on the perovskite layer dynamically at 2500\\u202frpm for 40\\u202fs in order to prevent the PC71BM layer from damage since both Spiro-OMeTAD and PC71BM can dissolve in chlorobenzene. For better hole transport, an additional layer of thin MoO3 film (6\\u202fnm) was deposited on top of the Spiro-OMeTAD layer via thermal evaporation []. Finally, 10\\u202fnm thin Ag and 35\\u202fnm MoO3 layers were deposited on the Spiro-OMeTAD/MoO3 HTL layer through a shadow mask via thermal evaporation in vacuum at a pressure of 1\\u00d710\\u22126 mBar. The device area was fixed to be 0.12\\u202fcm2 by using a metal shadow mask. For each perovskite layer thickness, at least six ST cells were fabricated.\\n\\nThe PC71BM and perovskite film thicknesses were measured by an Alpha-Step D600 profiler. A MATLAB script was developed based on the code developed by Burkhard and Hoke [] to simulate the optical electric field inside the device and the resulting exciton generation rate at different perovskite layer thicknesses. The surface roughness of the perovskite layers was extracted from atomic force microscopy (AFM) images using a Bruker Dimension ICON SPM. FEI Nova NanoSEM 230 FE-SEM was used to capture the perovskite surface topology images. X-ray diffraction (XRD) with Cu K\\u03b1 radiation was performed at an angle ranging from 10\\u00b0 to 60\\u00b0 by step-scanning with a step size of 0.02\\u00b0. The current density\\u2013voltage (J\\u2013V) measurements were performed using an IV5 solar cell I V testing system from PV Measurements, Inc. (using a Keithley 2400 source meter) under an illumination power of 100\\u202fmW/cm2 by an AM 1.5G solar simulator (Oriel model 94023A; 100\\u202fmW/cm2). During the J-V measurements of the ST cells, the illumination was always from the ITO side (bottom illumination). For the optical characterization of the ST films, a UV\\u2013Vis spectrophotometer (LAMBDA 950 UV/Vis Spectrophotometer) was used. External quantum efficiency (EQE) measurements were performed using a QEX10 spectral response system (PV measurements, Inc.). The resistivity of the MoO3/Ag/MoO3 back electrode was measured by using a four point probe system (Jandel model RM3).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag | MoO3,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Ethanol, diethyl ether, anhydrous dimethylformamide (DMF) (99.8%), anhydrous dimethylsulfoxide (DMSO) (99.9%), anhydrous ethanol, anhydrous diethyl ether (99.9%), lanthanide chloride (LaCl3\\u00b75H2O, 99.8%) and anhydrous tin chloride (SnCl2, 99.95%) were purchased from Wako, Japan. PbI2 and methylammonium iodine (MAI) was purchased from Deysol. Spiro-OMeTAD was purchased from the Ningbo Borun New Material Corporation. 4-Tert-butylpyridine (t-BP), and Li-bis-(trifluoromethanesulfonyl) imide (Li-TFSI) were purchased from Alfa-Aesar. All solvents were used without any further purification.\\n\\nFluorine-doped tin oxide (FTO) glass was chemically etched (Zn powder and 2\\u202fM HCl) to attain a partial etching pattern with a width of roughly 5\\u202fmm. The etched FTO substrate was then cleaned with a surfactant and successively rinsed with acetone, ethanol and deionized water and finally dried in an oven. 0.189\\u202fg SnCl2 was dissolved in 10\\u202fmL of absolute ethyl alcohol (0.1\\u202f\\u202fmol/L) with an extra 36\\u202f\\u03bcL of deionized water. For the lanthanide doping precursors, lanthanide (III) chloride was dissolved in absolute ethyl alcohol to form a solution with a 0.8\\u202fmol/L concentration. Different dosage, 1\\u202f\\u03bcL, 2.5\\u202f\\u03bcL, and 5\\u202f\\u03bcL LaCl3 solution were added to the 1\\u202fmL tin precursor to obtain 1%, 2.5%, and 5% molar ratio doped samples, respectively. All the precursor solutions were filtered through a 0.22\\u202f\\u03bcm PTFE filter before use. The precursors were spin coated on a clean FTO glass at 2000\\u202frpm for 30s, then annealed at 100\\u202f\\u00b0C for 10\\u202fmin and at 180\\u202f\\u00b0C for 1\\u202fh.\\n\\nA device with an n-i-p regular planar structure of FTO/SnO2/MAPbI3/Spiro-OMeTAD/Au was fabricated in a N2-filled glove box. The precursor solution of the one-step perovskite deposition was prepared by dissolving 0.22g methylammonium iodide (CH3NH3I) and 0.64\\u202fg lead iodide (PbI2) in a solution of 800\\u202f\\u03bcL DMF and 200\\u202f\\u03bcL DMSO (4:1, v:v), then stirred for 2\\u202fh at 60\\u202f\\u00b0C. The HTL solution was prepared by dissolving 72.3\\u202fmg of spiro-OMeTAD, 28.8\\u202f\\u03bcL of 4-tert-butylpyridine, and 17.5\\u202f\\u03bcL of lithium bis-(trifluoromethanesulfonyl) imide (Li-TFSI) (520\\u202fmg Li-TFSI in 1\\u202fmL acetonitrile) in 1\\u202fmL of chlorobenzene. All solutions were filtered through a PTFE filter (0.2\\u202f\\u03bcm pore size) before use. After the SnO2 or La:SnO2 layer was treated by UV-Ozone for 15\\u202fmin, the MAPbI3 precursor was spin-coated at 4000\\u202frpm for 30\\u202fs. A 150\\u202f\\u03bcL of ethyl acetate was dropped on top of the perovskite precursor 20s before the end. Afterward, the perovskite layer was sintered at 100\\u202f\\u00b0C for 10\\u202fmin. A 75\\u202f\\u03bcL of spiro-OMeTAD was spin coated at 4000\\u202frpm for 30s. Before the device was tested, 80\\u202fnm Au was thermally evaporated on the device at a ratio of 0.5\\u202f\\u00c5/s.\\n\\nThe X-ray diffraction (XRD) was scanned from 5\\u00b0 to 80\\u00b0 at the rate of 0.01\\u00b0s\\u22121 using an X-ray diffractometer (Rigaku Co., Ltd., Tokyo, Japan) with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.54056\\u202f\\u00c5). The field emission scanning electron microscope (FE-SEM) (JSM-6701, JEOL) was used to capture the morphology of the perovskite films. A UV-VIS-NIR spectrophotometer (V-670, JASCO Co., Ltd., USA) was measured to characterize the optical properties of the samples. The Fourier transform infrared spectroscopy (FTIR) was carried out using a spectrometer (4100, Jasco Instruments, USA). The IPCE was applied to record the perovskite absorption by monochromatic illumination (A 300\\u202fW Xenon arc lamp through a Nikon G250 monochromator). The transient photovoltage decay measurements were carried out using a 630-nm diode laser via the 5ns pulse duration and frequency of 4\\u202fHz. The voltage responses from the device were recorded using a DS-5554 Iwatsu digital oscilloscope. The electrochemical impedance spectroscopy (EIS) was carried out by the 1255\\u202fB Solartron Analytical. The current response to voltage (J-V) curve was measured by a Keithley 2450 solar simulator interfaced with a Xenon lamp (Bunko Keiki BSOX150LC) at 100\\u202fmW\\u202fcm\\u22122 under AM 1.5G conditions. The cell area was controlled at 0.08\\u202fcm2 by a black metal mask to measure the photovoltaic performance of the devices. The valence band of the SnO2 films was measured using photoelectron yield spectroscopy (KV205-HK energy instrument, Japan). When the SnO2 layer is activated by the certain incident light, the photoelectron current is detected by the sensor. The output data are photo energy (Eg) and yield of photoelectrons (Yield). The resolution of PYS was 0.01\\u202feV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"ITO/PEDOT:PSS/PEG-200/CH3NH3PbI3/PC60BM/Ag devices were fabricated on indium tin oxide (ITO)-coated glass substrates with 12\\u202f\\u03a9/sq. The ITO substrates were cleaned by sequential ultrasonic treatment in detergent, deionized water, acetone, and isopropyl alcohol for 30\\u202fmin each and then dried for 2\\u202fh. Then, the ITO substrates were treated by the ultraviolet before the next procedure. After that, poly(3,4-ethylenedioxythiophene): polystyrene sulfonic acid (PEDOT:PSS) (Clevios 4083) was spin-coated on the substrates and dried at 150\\u202f\\u00b0C for 30\\u202fmin. While the substrate reached room temperature, PEG layer was carried out to deposited on the top of PEDOT:PSS layer.\\nPerovskite precursor solution was combined with methylammonium iodide and lead (II) chloride (Sigma\\u2013Aldrich) at a 3:1\\u202fM ratio, which dissolved in N,N-Dimethylformamide (DMF, Sigma\\u2013Aldrich). Prior to device fabrication, the precursor solution was stirring at 60\\u202f\\u00b0C overnight in an Ar filled glove box, then filtered with a 0.45\\u202fnm PTFE filter. After spin coating on the PEDOT:PSS layer at 4000\\u202frpm for 60\\u202fs, the films were annealed on a hotplate in the glovebox at 80\\u202f\\u00b0C for 90\\u202fmin. The PCBM solution (20\\u202fmg/ml in chlorobenzene) was spin-cast at 1000\\u202frpm for 2\\u202fmin on top of the perovskite layer. Finally, a 90-nm-thick aluminum cathode (deposition rate of 1.0\\u202f\\u00c5/s) was deposited on the active layer through a shadow mask to give a device area of 0.060\\u202fcm2 under a vacuum level of 10\\u22126\\u202fTorr.\\n\\nThe PEG solution was prepared by different volume (0, 10\\u202f\\u00b5L, 20\\u202f\\u00b5L, 30\\u202f\\u00b5L, 40\\u202f\\u00b5L, 60\\u202f\\u00b5L) of PEG were added in acetone/ethanol (240\\u202f\\u00b5L/1680\\u202f\\u00b5L) system. The samples were assigned as S0, S1, S2, S3, S4, and S5 according to the PEG contents. After various volume of PEG solution were spin-coated on the top of PEDOT:PSS layer at 1500\\u202frpm, 15\\u202fs. Then, the sample was heated at different temperatures (100, 120, 140\\u202f\\u00b0C) and times (5, 10, 15, 20\\u202fmin).\\n\\nThe evaluation performance of the perovskite solar cells was studied by recording the current-voltage (I-V) characteristics of the unsealed type cell under illumination of AM1.5 (1\\u202fSun; 100\\u202fmW\\u202fcm\\u22122) and by using a solar simulator (Oriel, 91167). The electrical impedance spectra (EIS) was recorded over a frequency range of 0.1\\u2013106\\u202fHz under AM 1.5 (100\\u202fmW\\u202fcm\\u22122) conditions at 25\\u202f\\u00b0C. The optical transmittance and absorption spectra measurements were performed with a Shimadzu UV-3600 UV\\u2013vis spectrophotometer in the wavelength from 300 to 900\\u202fnm.\\nThe surface morphology was analyzed by using a field emission scanning electron microscope (Zeiss SIGMA FESEM). The atomic force microscopy (AFM) images were taken with an AFM system (Shimadzu Corporation, Model SPM9700). X-ray diffraction (XRD) patterns were obtained by Bruker D8 advanced X-ray diffractometer by using Cu-Ka radiation at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS | PEG,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials: lead (II) iodide (PbI2) and Methylamine iodide (MAI) were purchased from Xi\\u2019an Polymer Light Technology Corp. Poly(3,4-ethylenedioxythiophene):poly (styrenesulfonate) (PEDOT: PSS, PVP AI4083), Chlorobenzene (CB) and Cetyl trimethyl ammonium bromide (CTAB) were purchased from Sigma-Aldrich. Anhydrous N,N-Dimethylformamide (DMF), dimethyl sulfoxide (DMSO) and [6,6]-Phenyl-C61-butyric Acid Methyl Ester (PC61BM) were purchased from Aladdin.\\nFabrication of the device: ITO layers on glass substrates, with a sheet resistance of 8\\u202f\\u03a9/\\u25a1(Pilkington), were cleaned with alkaline detergent, acetone, absolute ethanol and deionized water for 15\\u202fmin, the cleaned substrates were UV-ozone treated for 15\\u202fmin, respectively, before they were used for spin-coating. The PEDOT:PSS solution with different amount of CTAB was spin-coated onto the ITO substrates at 4000\\u202frpm for 30\\u202fs and annealed at 150\\u202f\\u00b0C for 10\\u202fmin. MAPbI3 precursor solution was prepared by mixing 159\\u202fmg CH3NH3I, 462\\u202fmg PbI2 in anhydrous DMF:DMSO (9:1, v/v), then filtered with 0.22\\u202f\\u03bcm nylon filter to obtain a clear solution. The MAPbI3 precursor solution was spin-coated on the PEDOT: PSS coated substrates at 3000\\u202frpm for 30\\u202fs and 200\\u202f\\u03bcL chlorobenzene was slowly dripped onto the surface of the film 10\\u202fs after the beginning of spin-coating. Perovskite layer was annealed at 100\\u202f\\u00b0C for 20\\u202fmin resulting in a thickness of 300\\u202fnm. After cooling to room temperature naturally, 20\\u202fmg/ml PC61BM dissolved in CB was spin-coated onto the perovskite films at 3000\\u202frpm for 30\\u202fs. Finally, Ag electrode was deposited using thermal evaporation at a constant evaporation rate of 0.1\\u202fnm/s. Except for the fabrication of PEDOT:PSS layer, the whole process is carried out in glove-box under Ar condition at room temperature.\\nCharacterization: Atom Force Microscope (AFM) images were obtained using a Multimode 8 atomic force microscope using tapping mode. The photovoltaic performance of PSCs was recorded using a Keithley 2400 source meter with a delay time of 100\\u202fms under one-sun, AM 1.5G (100\\u202fmW/cm2) illumination with a solar light simulator (Newport Oriel Sol3A Class AAA, 64023A Simulator), which was calibrated using a National Renewable Energy Laboratory (NREL) standard Si solar cell. The error range of the sun simulator was 1000\\u202f\\u00b1\\u202f3\\u202fW/m2. Electrochemical Impedance Spectroscopy (EIS) measurements were conducted by an electrochemical workstation (CHI660d) (0.1\\u202fMHz\\u201310\\u202fHz) and the fitting software was Zview software. The UV\\u2013vis light absorption measurement was performed by using an ultraviolet\\u2013visible (UV\\u2013vis) spectrophotometer (Shimadzu UV-3101 PC). The external quantum efficiency (EQE) measurements were obtained on a Keithley 2000 multimeter as a function of the wavelength from 350 to 800\\u202fnm on the basis of a Spectral Products DK240 monochromator. The active area of the cell is 0.1\\u202fcm2. All samples were measured in air (25\\u202f\\u00b0C). The steady-state Photoluminescence (PL) spectra were obtained by Horiba Fluorolog FL-3 and the excitation wavelength was set at 532\\u202fnm for the perovskite films on glass substrates. The work function of studied PEDOT: PSS films was obtained from Ultroviolet Photoelectron Spectrometer (UPS).\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 30.0; 30.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 720,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 20,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"To prepare the perovskite precursor solution with or without PbF4 or PbF2, firstly, PbI2 (1.3\\u00a0mmol, Sigma-Aldrich) and MAI (1.3\\u00a0mmol, Liaoning You Xuan Technology Co., Ltd) powders were mixed in 1\\u00a0mL anhydrous GBL/DMSO (v/v\\u00a0=\\u00a07/3, J&K Scientific Ltd.). Then, we prepared 1% PbF4 or PbF2 or PbF4/PCBM in GBL/DMSO solutions firstly, and then add to 1.3\\u00a0M MAPbI3 solution after dilution proportionally. The PbF4 (Alfa Aesar) or PbF2 (J&K Scientific Ltd.) were added with mass ration of 0, 0.01%, 0.03%, 0.05%, 0.1% and 0.2%. The precursor solution with PbF4/PCBM (Aladdin) was obtained by adding 0.03% PbF4 firstly, and then adding PCBM with mass ration of 0, 0.01%, 0.05%, 0.075%, 0.1% and 0.2%. The solutions were stirred at 65\\u00a0\\u00b0C overnight, and then filtered before using in perovskite thin-film deposition. ITO-coated glass (15\\u00a0\\u03a9 per square) with 12.5\\u00a0\\u00d7\\u00a012.5\\u00a0mm size was etched by (Zn\\u00a0+\\u00a0HCl) solution to form three separated electrodes. The etched substrates were cleaned by ultrasonication in washing solution, deionized water, ethanol, acetone and isopropanol, successively. After drying, a\\u00a0~\\u00a050\\u00a0nm thick PEDOT:PSS (CleviousTM P VP AI 4083) was spin-coated onto the ITO substrate and then dried at 140\\u00a0\\u00b0C for 20\\u00a0min. After cooling to room temperature, the perovskite film was deposited by spin-coating at 4500\\u00a0rpm for 30\\u00a0s using the prepared precursor solutions which were maintained at 65\\u00a0\\u00b0C during the whole procedure, and toluene was dripped in the last 5\\u00a0s. After that, the perovskite films were heated at 100\\u00a0\\u00b0C for 10\\u00a0min. After cooling to room temperature, PCBM (20\\u00a0mg\\u00a0mL\\u22121) was deposited by spin-coating at 2000\\u00a0rpm for 30\\u00a0s. After dried overnight, 1\\u00a0nm of LiF and100 nm of silver was thermally evaporated on top of the device to form the contact.\\n\\nDevices were tested in air ambient. The J-V curves of the PSCs were measured using a Newport solar simulator with a Keithley 2400 Source Meter under an AM 1.5G condition. The external quantum efficiency (EQE) spectra were measured by a Newport QE 200 system. UV\\u2013vis spectra were measured using Agilent Cary 5000 UV\\u2013vis-NIR spectrometer. The steady-state PL spectra were performed on a Hitachi F-7000 Fluorescence Spectrophotometer. The SEM images were recorded on a Hitachi S4800 with an acceleration voltage of 10\\u00a0kV. The AFM characterizations were obtained by a tapping mode on a Bruker Dimension EDGE. The XRD spectra were carried out with a Bruker D8 Advance diffractometer with Cu K\\u03b1 radiation (\\u03bb\\u00a0=\\u00a01.5406\\u00a0\\u00c5). The GIXRD data were measured using the X-ray diffuse scattering station on the 1W1A beam line in the Beijing Synchrotron Radiation Facility (BSRF). The fluorescence-yield XAFS at Pb L3-edge was collected at room temperature at the BSRF on 1W1B beam line.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Lif,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: PbF4,\\n Perovskite_deposition_solvents: GBL; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 30; 30,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 720,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: ,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Pre-patterned indium doped tin oxide (ITO) coated glass (15 \\u03a9/cm2), PbI2 (99.9%, Sigma Aldrich), PbCl2 (99.9%, Sigma Aldrich), methylammonium iodide (Dyesol), dimethylformamide (DMF, dry, Sigma Aldrich), poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS, Clevios pH 1000), Zonyl\\u00ae FS-300 fluorosurfactant (40% in H2O, Fluka), dimethyl sulfoxide (DMSO, Anal R, VWR chemicals), [6,6]-phenyl-C61-butyric acid methyl ester (PCBM, SolenneBV), chlorobenzene (GPR, VWR chemicals), chloroform (Anal R, VWR chemicals), isopropanol (Anal R, Fisher chemicals) were used as received. Precursor mixed halide solutions were prepared with molar ratio (0.5PbCl2+0.5PbI2+2.2CH3NH3I) (640 mg/ml in DMF) stirred overnight at room temperature in ambient air and filtered with 0.45 \\u00b5m PTFE filter. Perovskite thin films for UV\\u2013vis optical absorption and photoluminescence measurements were prepared by spin-coating at 4000 rpm on different substrates from 50% diluted solution of the precursor solution. The fabrication of planar heterojunction perovskite solar cells started with cleaning pre-patterned ITO coated glass substrates sequentially with acetone, Hellmanex\\u00ae, deionized water and isopropanol in an ultrasonic bath. Different volumes of PEDOT:PSS (Clevios PH1000), DMSO and Zonyl FS300 were carefully mixed. The formulated PEDOT:PSS dispersion was filtered through a 0.45 \\u00b5m RC filter and spin-coated at 1000 rpm for one minute. The PEDOT:PSS layer was then patterned and annealed for 10 min at 110 \\u00b0C, cooled, rinsed with isopropanol by spinning at 4000 rpm to remove the excess surfactant (Zonyl) from the surface, and then annealed for another 10 min at the same temperature. The typical thickness of PEDOT:PSS was found to be ~130 nm. The precursor solution was spin-coated (1500 rpm for 20 s and then at 2000 rpm for 5 s) on top. After spin-coating, the substrates were immediately transferred to a hot plate at 110 \\u00b0C where the colorless wet film is turned into glassy dark brown layer in few seconds and then further annealed for 45 min in ambient air. The procedure resulted in a 350\\u2013400 nm thick perovskite absorber layer. PCBM (20 mg/ml in 1:1 volume ratio of chlorobenzene and chloroform) was spin coated (1500 rpm for 15 s and then at 2000 rpm for 15 s) on top of the perovskite layer, which yields a thickness of 50\\u201370 nm. The entire processing up to this step is performed in ambient air. The sample was then transferred to a vacuum chamber located inside a nitrogen-filled glove box for the evaporation of the aluminum top electrode at <3\\u00d710\\u22126 mbar. The solar cells were encapsulated with a glass cover using a UV-curable epoxy sealant (Ossila E131), with a UV exposure time of 6 min. The fabricated solar cells with an active area of ~0.17 cm2 were tested on a LOT-QD solar simulator (LS0821). The radiation intensity was adjusted using a calibrated reference silicon diode to 100 mW/cm2. External quantum efficiencies (EQEs) were recorded by using a lock-in amplifier (SR830, Stanford Research Systems) and a Jaissle 1002 potentiostat. The potentiostat operated in the two electrode configuration is a high performance current amplifier with a variable gain ranging from 10 to 108 V/A. In addition, the potentiostat allows measuring the EQE-spectra at different applied voltages. The devices were illuminated by monochromatic light from a xenon lamp passing through a monochromator (Oriel Cornerstone) with typical intensities in the range of 10\\u2013100 \\u03bcW. A filter wheel holding long-pass filters and a mechanical chopper was mounted between the xenon lamp and the monochromator. Chopping frequencies in the range of 73\\u2013273 Hz were used. A calibrated silicon diode (Hamamatsu S2281) was used as a reference. A halogen lamp (Philips 50 W, 12 V) provided a variable white light bias to the solar cells while the EQE was measured. To determine the power conversion efficiency of the prepared solar cells, the illuminated area of the solar cell was defined using a shadow mask (0.13 cm2). In a first step the current-voltage curve was recorded with a Keithley 2400 source-measurement unit under illumination (solar simulator). The voltage was increased slowly (20 mV/s) and the current-voltage curve was determined close to steady state-conditions. To check for hysteresis a reverse voltage scan was performed decreasing the voltage by 20 mV/s. In a second step the short circuit current was recorded (steady state value) with a Keithley 2400. A maximum-power-point tracking algorithm was used to measure the steady-state power output of the solar cell. The external quantum efficiency was determined operating the solar cell under short circuit conditions and 1 sun illumination. The short circuit current calculated using the EQE-data allowed the determination of the spectral mismatch factor (MM) of our solar simulator. We found values >0.95 for the investigated devices. This mismatch factor was used to correct the maximum power point measurement. UV\\u2013vis absorption spectra of perovskite films were recorded using a double beam UV\\u2013vis spectrometer (Perkin Elmer 1050) equipped with an integrating sphere. A Bruker Dektak XT profilometer was used to measure layer thicknesses. Photoluminescence and electroluminescence spectra of various devices were measured using a Shamrock SR-303i monochromator and an Andor iDus Si-CCD. Samples were excited at 473 nm (5 mW) using a solid-state laser or a supercontinuum light source (NKT EXB6) connected to a VIS-NIR SuperK Select Box. A set of long-pass filters was used to avoid any distortion of the recorded spectra by the laser light. Electroluminescence spectra were recorded while applying different potentials with a Keithley 2401. The integrated electroluminescence was detected measuring the emitted photon current with a calibrated large-area Si-photodetector (Hamamatsu S2281) positioned close to the sample. Preliminary stability studies were performed on an ORIEL solar simulator. Surface and cross section scanning electron microscopy (SEM) images were made using a ZEISS 1540XB CrossBeam Scanning microscope equipped with a focused ion-beam (FIB) unit. Gas chromatography coupled with mass spectrometry (GC\\u2013MS) measurements were performed on an 6890 GC with a 5935C mass selective detector (both Agilent Technologies, Waldbronn, Germany) equipped with a MPS2-XL headspace autosampler from Gerstel (M\\u00fclheim/Ruhr, Germany). The carrier gas used was helium and a ZB-624 GC-column, 60 m\\u00d70.25 mm I.D. film thickness 1.40 \\u00b5m (Phenomenex, Aschaffenburg, Germany) was employed. 500 \\u03bcl of the gas-phase above PEDOT:PSS-films coated on glass substrates was analyzed after the films were heated to 140 \\u00b0C for 10 min; the MS was operated in the full-scan mode.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 110,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.13,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were used as received without further purification. Titanium tetraisopropoxide (TTIP, 97%), lead iodide (PbI2), N,N-dimethylformamide (DMF), dimethylsulfoxied (DMSO), acetonitrile (ACN), toluene, Li-bis(trifluoromethanesulfonyl) imide (Li-TFSI), tert-butylpyridine (t-BP), and formamidinium iodide (FAI), and methylammonium bromide (MABr) were purchased from Sigma-aldrich. Ethanol (EtOH), iso-propanol (IPA), toluene and nitric acid (HNO3) were purchased from Samchun. Poly-triarylamine (PTAA) was purchased from EM index Co., Ltd.\\n\\nWe first synthesized TiO2 nano-sol by sol-gel method. 84\\u202fg of TTIP was poured dropwise into 525\\u202fg of distilled water with stirring at 80\\u202f\\u00b0C and the white precipitates were formed immediately. After these were dispersed in solution, 14\\u202fg of HNO3 was added in solution and proceeded the reaction for 15\\u202fh. The TiO2 nano-sol was then fully dried at 60\\u202f\\u00b0C for 18\\u202fh in a convection oven. The TiO2 nano-powder was then re-dispersed in H2O, EtOH, DMSO, and DMF to prepare TiO2 nano-sol with specific wt% of concentration.\\n\\nSize of TiO2 nanoparticles were characterized by transmission electron microscope (TEM, JEM-2100F, JEOL). Their crystal structures were characterized X-ray diffraction (XRD, D8 advance, Bruker) machine using Cu K\\u03b1 radiation at 40\\u202fkV and 40\\u202fmA and scanning at 6\\u00b0/min. The topographic image and height profile of TiO2 films were obtained in a non-contact mode of AFM (Park system, model XE-100). The UV\\u2013Vis transmission spectra were obtained using a UV-2450PC spectrophotometer (SHIMADZU, Japan).\\n\\nTo check I-V characteristics of TiO2 ETL prepared by 5, 10, and 20\\u202fwt% nano-sol in DMF, each solution was spin-coated on an oxygen plasma treated ITO/glass substrate at 3000\\u202frpm for 30\\u202fs and heat-treated on a hot plate at 100\\u202f\\u00b0C for 30\\u202fmin. The heat-treatment ensures the following orthogonal processability of perovskite solution in DMF because the remained hydroxyl groups on the surface of TiO2 nanoparticles can be aged by condensation reaction so the TiO2 nanoparticles are tightly bonded by each other. For fabrication of rigid FAPbI3-xBrx perovskite solar cells, we deposited a TiO2 ETL by spin-coating 10\\u202fwt% of TiO2 nano-sol in DMF on an oxygen plasma treated ITO/glass substrate at 3000 rom for 30\\u202fs and dried it on a hot plate at 100\\u202f\\u00b0C for 30\\u202fmin. FAPbI3-xBrx perovskite film was then deposited on the TiO2/ITO/glass substrate. To make FAPbI3-xBrx perovskite films, we synthesized a PbI2(DMSO)2 complex by dissolving 50\\u202fg PbI2 in 150\\u202fml DMSO at 60\\u202f\\u00b0C for 30\\u202fmin and slowly dropped 350\\u202fml toluene into the PbI2 solution. Then, we filtered the white precipitate and annealed it in a vacuum oven at 60\\u202f\\u00b0C for 5\\u202fh to make PbI2(DMSO). We then spin-coated the 1\\u202fM PbI2(DMSO) in DMF at 3000\\u202frpm for 30\\u202fs and consecutively spin-coated 0.5\\u202fM FAI: MABr (0.85:0.15\\u202fmol:mol) mixture solution in IPA at 5000\\u202frpm for 30\\u202fs. The films were dried on a hot plate at 150\\u202f\\u00b0C 20\\u202fmin. PTAA hole conductor with additives was deposited on the MAPbI3/TiO2/ITO substrates by spin-coating a mixture of PTAA/toluene (15\\u202fmg/1\\u202fml) with 7.5\\u202f\\u03bcl Li-TFSI/ACN (170\\u202fmg/1\\u202fml) and 7.5\\u202f\\u03bcl t-BP/ACN (1\\u202fml/1\\u202fml) additives at 3000\\u202frpm for 30\\u202fs. Finally, an Au counter electrode was deposited by thermal evaporation. For flexible perovskite solar cells, we only changed the rigid glass substrate to flexible PET/ITO substrate and fabricated devices by following the same procedure. The active area was fixed at 0.16\\u202fcm2. All devices fabricated under relative humidity below 25%. The current density-voltage curves were measured by a solar simulator (Peccell, PEC-L01) with a potentiostat (IVIUM, IviumStat) at under illumination of 1 sun (100\\u202fmW/cm2 AM 1.5\\u202fG), which is calibrated by Si-reference cell certificated from JIS (Japanase Industrial Standards). J-V curves of devices were measured by masking metal mask with aperture of 0.096\\u202fcm2. External quantum efficiency (EQE) was measured by a power source (ABET, 150\\u202fW Xenon lamp, 13014) with a monochromator (DONGWOO OPTRON photovoltage were measured by potentiostat (IVIUM, IviumStat).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAPbBr0.45I2.55,\\n Perovskite_composition_short_form: FAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 150,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 20.0,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.096,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The PSC active layer is prepared according to our previously optimized procedure using excess Pb in the precursor, which is briefly described here []. Poly (3,4-ethylene dioxythiophene): poly (styrene sulfonate) (PEDOT: PSS), purchased from Ossila, was spin-coated onto ITO substrates at 4000\\u202frpm for 60\\u202fs followed by thermal annealing at 130\\u202f\\u00b0C for 15\\u202fmin. Methylammonium iodide (MAI) was purchased from Dyesol and lead acetate trihydrate (PbAc2. 3H2O) was purchased from Alfa Aesar and both were used as received. 2.7\\u202fmmol MAI and 0.9\\u202fmmol PbAc2.3H2O were dissolved into 1\\u202fmL anhydrous dimethyl formamide (DMF) solution resulting in a solution concentration of 0.9\\u202fM. For preparing Pb excessive solution, (MAI/PbAc2\\u202f=\\u202f3:1.05) were used. This solution was then spin-coated onto the PEDOT layer at 4000\\u202frpm for 60\\u202fs followed by an anneal at 80\\u202f\\u00b0C for 12\\u202fmin. PCBM dissolved into chlorobenzene (20\\u202fmg/ml) was spin-coated on the top at 1000\\u202frpm for 30\\u202fs. Zirconium acetylacetonate purchased from Aldrich was dissolved into different alcohols to prepare solutions of concentration 1\\u202fmg/ml. This was spin-coated onto the PCBM at 3000\\u202frpm for 30\\u202fs. For device fabrication, we thermally evaporated a 70\\u202fnm thick Al electrode that resulted in a device area of 0.2\\u202fcm2.\\nThe as-prepared devices were characterized for current-density measurements under simulated AM 1.5 solar irradiation (100\\u202fmW/cm2) which is a xenon-lamp based solar simulator (Spectra Physics, Oriel Instruments, USA). The steady-state photoluminescence (PL) spectra of the samples were tested using Reinshaw InVia spectroscopy system with a x100 objective lens and a laser source of wavelength 488\\u202fnm. The charge carrier lifetimes were measured by Picosecond Time-Correlated Single Photon Counting Spectrofluorometer (TCSPC). The PL decay time was observed at 775\\u202fnm after excitation from a Ti:S laser (Spectra Physics) at 425\\u202fnm The PL decay kinetics were fitted to a bi-exponential decay function. Surface morphology was measured using scanning electron microscopy (SEM-XL30 Environmental FEG (FEI) and atomic force microscopy (Bruker Multimode 8). X-ray diffraction analysis was done with a Rigaku diffractometer. The tension was 40\\u202fkV on the Cu anode and the filament current was 20\\u202fmA.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Zr(acac)4,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Acetate; H2O,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 25,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.2,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI), formamidinium Iodide (FAI), methylammonium bromide (MABr), cesium iodide (CsI), lead iodide (PbI2) and lead bromide (PbBr2) were purchased from Xi'an Polymer Light Technology Corporation. 2,2\\u2019-Bipyridine were purchased from Alfa Aesar. Zirconium(IV) acetylacetonate (Zr(acac)4) was purchased from Sigma-Aldrich. [,]-Phenyl C61 butyric acid methyl ester (PC61BM) was purchased from American Dyes Source, Inc.. All chemicals were used as received without further purification. NiOx NPs was prepared according to our previous report [] based on the method of Yin et al. [].\\n\\nFabrication of CsFAMA mixed-cation perovskite solar cells: ITO-coated glass substrates were cleaned by sonification in acetone, detergent, deionized water, and ethanol and dried in a baking oven at 60\\u202f\\u00b0C. To fabricate inverted photovoltaic devices, a NiOx anode interfacial layer was deposited on the pre-cleaned ITO-coated glass substrates by spin coating at 3000\\u202frpm and baked at 120\\u202f\\u00b0C for 20\\u202fmin. 2,2\\u2019-BiPy (0.05\\u202fmg\\u202fmL\\u22121 in ethanol) was spin-coated on the NiOx substrate at 4000\\u202frpm for 30\\u202fs and baked at 100\\u202f\\u00b0C for 10\\u202fmin. The perovskite precursor solution was composed of 1.376\\u202fM MABr, 1.376\\u202fM FAI, 1.5\\u202fM PbI2 and 1.5\\u202fM PbBr2 in DMF:DMSO (4:1 v:v) with the ratio of iodide based perovskite and bromide based perovskite maintained at 0.85:0.15. Then, 5%vol CsI (1.5\\u202fM in DMSO) was added into the precursor solution and stirred at 60\\u202f\\u00b0C till completely dissolved. The precursor solution was prepared with a two-step spin-casting process at 1000\\u202frpm with 200\\u202frpm/sec acceleration for 10\\u202fs and 5000\\u202frpm with 2000\\u202frpm/sec acceleration for 25\\u202fs. During the second step, ethyl acetate (150\\u202f\\u03bcL) was rapidly dropped in the middle of the substrates at 10\\u202fs before the end of spin coating. Then, the thin film was thermally annealed at 100\\u202f\\u00b0C for 60\\u202fmin. The thickness of the perovskite film was ca. 740\\u202fnm. PC61BM (20\\u202fmg\\u202fmL\\u22121) was prepared by spin coating chlorobenzene solution at 2500\\u202frpm for 30\\u202fs. After thermal annealing at 50\\u202f\\u00b0C for 5\\u202fmin, a Zr(acac)4 cathode interfacial layer (2\\u202fmg\\u202fmL\\u22121 in ethanol) was deposited by spin coating at 2000\\u202frpm for 40\\u202fs. Finally, the silver cathode layer (90\\u202fnm) was thermally evaporated onto the solution-processed layer under high vacuum (< 3\\u202f\\u00d7\\u202f10\\u22124 Pa). The effective area of cells was 0.0576\\u202fcm2, defined by shallow masks. All the steps except processing of NiOx were performed in the glove box.\\nFabrication of semi-transparent perovskite solar cells (ITO/NiOx or modified NiOx/semi-transparent MAPbI3/PC61BM/Zr(acac)4/Ag/CsF): MAPbI3 was prepared according to our previous report, using ethyl acetate (EA) and MACl solution (1\\u202fmg\\u202fmL\\u22121 in isopropanol) as the anti-solvents. [] The thickness of the perovskite film was 283\\u202fnm. The silver electrode (20\\u202fnm) and the CsF layer (15\\u202fnm) were thermally evaporated onto the solution-processed layer under high vacuum (< 3\\u202f\\u00d7\\u202f10\\u22124 Pa). The effective area of cells was 0.0576\\u202fcm2, defined by shallow masks. Other layers were prepared as the deposition condition mentioned above.\\nFabrication of single-carrier devices: Hole-only devices (ITO/NiOx or (NiOx/2,2\\u2019-BiPy)/MAPbI3/MoO3(15\\u202fnm)/Ag) were fabricated to estimate the trap states in the perovskite film. MAPbI3 was prepared according to our previous report, using EA as the anti-solvent. [] MoO3 was deposited by thermal evaporation under high vacuum (< 3\\u202f\\u00d7\\u202f10\\u22124 Pa). The effective area of cells was 0.0576\\u202fcm2, defined by shallow masks.\\n\\nDevice characterization: The current density\\u202f\\u2212\\u202fvoltage (J\\u2212V) characteristics were measured using a Keithley 2400 source meter. The photovoltaic devices were characterized from reverse scans using a calibrated AM 1.5\\u202fG solar simulator (SAN-EI ELECTRIC CO.,LTD.), under light intensity of 100\\u202fmW cm\\u22122.\\nPerovskite film characterizations: X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS) measurements were carried out on a Thermo Fisher Scientific ESCALAB 250Xi. They were performed in an ultrahigh vacuum (UHV) system with a base pressure better than 5\\u202f\\u00d7\\u202f10\\u22128 Pa. For XPS depth profile measurements, the perovskite precursor solution was composed of 0.917\\u202fM MABr, 0.917\\u202fM FAI, 1\\u202fM PbI2 and 1\\u202fM PbBr2. Scanning electron microscope (SEM) images were recorded on a HITACHI UHR FE-SEM SU8010. Tapping-mode atomic force microscopy (AFM) measurements were carried out on a Veeco Nanoscope V scanning probe microscope. X-ray diffraction (XRD) measurements were finished on a Bruker D8 ADVANCE X-Ray diffractometer. The steady-state photoluminescence spectra were performed on HORIBA Instruments Incorporated Fluorolog-3 fluorescence spectrophotometer. The steady-state photoluminescence spectra were excited at 420\\u202fnm. UV\\u202f\\u2212\\u202fVis\\u202f\\u2212\\u202fNIR absorption spectra were recorded on a SHIMADZU UV-3600 Plus UV\\u2013vis-NIR spectrophotometer. Other samples were prepared as the deposition condition mentioned in the CsFAMA mixed-cation PSC fabrication and deposited on NiOx substrates.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Zr(acac)4,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: NMP >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 60.0,\\n HTL_stack_sequence: NiO-np | 2,\\n2\\u2019-BiPy,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag | CsF,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0576,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The PEDOT:PSS dispersion was obtained following the Baytron P synthetic procedure. Poly(4-styrenesulfonate) (PSS, MW = 4.0 \\u00d7 105 g mol\\u22121) was used as both the dispersant and the dopant for PEDOT. A PSS and distilled water solution was bubbled using nitrogen gas (99.999%) for 60 min at a rate of 3 L min\\u22121 to prevent oxidation from the dissolved oxygen in the water. To this solution, EDOT monomer was added, and the solution was stirred using a mechanical stirrer for 30 min. The direct synthesis of the PEDOT:PSS dispersion was carried out by a Fe3+-catalyzed oxidative polymerization process. The oxidizing reagents iron(III) sulfate and sodium persulfate were dissolved in distilled water by sonication and added to the reaction solution. The polymerization was performed for 24 h at 10 \\u00b0C with bubbling nitrogen gas. After the polymerization of PEDOT:PSS, the product was mixed with a mixture of cation and anion ion exchange resins for 1 h and filtered with a 30 \\u03bcm mesh filter. Then, the PEDOT:PSS dispersion was homogenized with a high-pressure homogenizer at 1000 bar to prepare a well-dispersed solution. Finally, the dispersion was passed through a 5 \\u03bcm filter. To control the ratio of PEDOT to PSS, the PEDOT:PSS dispersion was synthesized by changing the mass ratio of the EDOT monomer to PSS. All the obtained PEDOT:PSS dispersions had a solid content of 1.1%.\\n\\nThe thickness of the films was measured using a surface profiler (Alpha-Step 500, KLA-Tencor). The PSS/PEDOT ratio and chemical composition on the film surface were determined by X-ray photoelectron spectroscopy (XPS, Thermo K-Alpha XPS, Thermo Fisher Scientific, West Palm Beach, FL, USA). The surface images of the polymer films were obtained using atomic force microscopy (AFM, Park Systems XE-100) in non-contact mode. Using UV photoelectron spectroscopy (UPS), the WF was determined from the secondary cutoff region (Ecutoff) and the Fermi energy (EFermi), which were clearly defined and calculated by using \\u03c6 = hv = 21.2 eV \\u2212 Ecutoff + EFermi, where hv = 21.2 eV is the incoming photon energy from the He I source and a \\u22125 V bias was applied to produce a clear boundary in the Ecutoff region. The transmittance spectra of the various PEDOT:PSS layers were obtained using a UV/Vis/NIR spectrophotometer (Varian Cary 5000 UV/Vis/NIR spectrophotometer).\\n\\nTo prepare the perovskite solution, methylammonium iodide (CH3NH3I, MAI) was synthesized according to a reported method. First, methylamine (27.86 mL, 40% in methanol) was reacted with hydroiodic acid (30 mL, 57 wt% in water, Aldrich) in a 250 mL round-bottomed flask at 0 \\u00b0C for 2 h with stirring. The precipitate was recovered via evaporation at 50 \\u00b0C for 1 h. MAI was dissolved in ethanol, recrystallized from diethyl ether, and dried at 60 \\u00b0C in a vacuum oven for 24 h. Lead iodide (PbI2, 99.999%), N,N-dimethylformamide (DMF, 99.8%) and dimethyl sulfoxide (DMSO, 99.5%) were purchased from Sigma-Aldrich.\\n\\nIndium tin oxide (ITO) glass substrates were cleaned using acetone and 2-propanol in a bath sonicator, followed by UV/ozone (Altech LTS) for 30 min. After cleaning, various PEDOT:PSS solutions with controlled weight ratios (1:0.5, 1:2.5, 1:5.0, and 1:12) and a conventional PEDOT:PSS solution (Clevios P VP AI 4083) were spin-coated on the ITO glass substrates at 4000 rpm for 30 s and were then heated at 150 \\u00b0C for 10 min on a hot plate. We used the solvent engineering method to form the perovskite layer. The prepared MAI powder and PbI2 in a 1 M MAPbI3 solution were stirred in a mixture of DMF and DMSO (7:3 v/v) at 70 \\u00b0C for 1 h. The completely dissolved solution was spin-coated on various PEDOT:PSS layers at 5000 rpm for 40 s. During spin-coating, toluene (1 mL) was dropped on the rotating substrate. After spin-coating, the film was heated at 100 \\u00b0C for 10 min. After forming the perovskite layer on the PEDOT:PSS layer, a 2 wt% PC60BM in chlorobenzene solution was then spin-coated on the perovskite layer at 1000 rpm for 60 s. Finally, an Ag electrode with a thickness of 150 nm was deposited on the PC60BM layer under 2 \\u00d7 10\\u22126 Torr vacuum in a thermal evaporator.\\n\\nTo improve the accuracy of the device area, the active layer region of the PSCs was examined with a video microscope (Sometech, SV-35) using an aperture placed on the bottom of the cell; the aperture area was 11.430 mm2. The current\\u2013voltage (J\\u2013V) characteristics of the PSCs were measured with a Keithley Series 2400 Source Measure Unit under AM 1.5 white light (100 mW cm\\u22122) illumination. A solar simulator (Oriel Sol 3A, class AAA) with a filtered 450 W xenon lamp was employed as the light source, and proper adjustments were made with a Si reference cell (VLSI standards, Oriel P/N 91150 V) in order to produce a 1 sunlight intensity of 100 mW cm\\u22122. The external quantum efficiency (EQE) was measured using a Solar Cell QE/IPCE Measurement System (Zolix Solar Cell Scan 100). Impedance spectroscopy was conducted using an impedance analyzer (IVIUM Tech.). A small AC voltage of 20 mV was applied at 0 V and VOC under 1 sun illumination (AM 1.5G, 100 mW cm\\u22122). The AC voltage was applied with a frequency ranging from 1 MHz to 10 Hz.\\n\\nThe cross-sectional and surface morphologies of the perovskite films were measured by field-emission scanning electron microscopy (FE-SEM, JEOL, JSM-7001F). The crystal structural characteristics were obtained by XRD (SmartLab, Rigaku) with Cu K\\u03b1 radiation (1.5418 \\u00c5).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1143,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI) was provided by the Phosphor Bank at Pukyong National University. If not specified, all other chemicals were purchased from Aldrich. A 1.2 M perovskite precursor solution was prepared by dissolving equimolar amounts of PbI2 and MAI into a mixture of N,N-dimethylformamide (DMF, 99.8%), N-methly-2-pyrolidinoine (NMP), \\u03b3-butyrolactone (GBL), and DMSO cosolvents at various volume ratios. The solution was then stirred at 70 \\u00b0C overnight and filtered with 0.45 \\u03bcm nylon filters before use.\\n\\nThe solar cells were fabricated with a glass/indium tin oxide (ITO)/poly(3,4-ehtylenedioxythiophene):poly (styrene sulfonate) (PEDOT:PSS)/MAPbI3/phenyl-C61-butyric acid methyl ester (PC61BM)/Al configuration. The glass/ITO substrates were cleaned with water, ethanol, and acetone in an ultrasonic bath for 15 min in sequence, and subsequently treated in a UV-Ozone cleaner for 15 min. The PEDOT:PSS (Baytron PVP Al 4083) layer was fabricated by first spin coating PEDOT:PSS onto the substrates at 4500 rpm for 40 s and then annealing it at 150 \\u00b0C for 20 min, resulting in a thickness of 50 nm. Then, the substrates were transferred into a N2-filled glovebox. The perovskite precursor solution was spin-coated onto the ITO/PEDOT:PSS layer at 5000 rpm for 15 s. Antisolvent treatment was used according to a previously reported study. Afterwards, PC61BM (20 mg mL\\u22121 in chlorobenzene) was deposited by spin coating at 1500 rpm for 30 s, forming an 80 nm transporting layer. Then, the substrate was annealed at 100 \\u00b0C for 10 min. Finally, Al electrodes with a thickness of 100 nm were deposited by evaporation under high vacuum (<2 \\u00d7 10\\u22126 Torr) through a shadow mask. The device area was defined as 0.04 cm2.\\n\\nX-ray diffraction (XRD) experiments were conducted using a Philips X-ray diffractometer with Cu K\\u03b1 radiation. The surface morphologies of the perovskite films were obtained by scanning electron microscopy (SEM, S-2700, Hitachi, Japan). UV-Vis absorption spectra of the perovskite films were collected on a Varian 5E UV/Vis/NIR spectrophotometer. Size distributions of the precursor solutions were measured using a Zeta potential analyzer (Malvern). Contact angles were measured using Smartdrop. Photocurrent density\\u2013voltage (J\\u2013V) curves were measured under AM 1.5G irradiation (100 mW cm\\u22122) with a solar simulator and a Keithley 2400 source meter. The light intensity was adjusted by a calibrated Si solar cell. External quantum efficiency (EQE) was measured under direct current (dc) mode, where a Xenon lamp was used as a light source for generating a monochromatic beam.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The synthesis of compounds (2) and (3) followed an earlier published synthetic procedure.\\nSynthesis of 2,7-bis(trimethylstannyl)naphtho[1,2-b:5,6-b\\u2032]dithiophene (5). n-Butyllithium (2.4 M solution in hexane, 3.03 mL, 7.28 mmol) was added dropwise to a solution of compound (4) (500 mg, 2.08 mmol) in dry THF (50 mL) at \\u221278 \\u00b0C. The mixture was stirred at this temperature for 30 min and then at room temperature for 1 h. After cooling down to \\u221278 \\u00b0C, Me3SnCl (1 M solution in hexane, 8.32 mL, 8.32 mmol) was added dropwise. After stirring for 30 min at this temperature, the reaction was allowed to warm up to room temperature and stirred overnight. The reaction mixture was then extracted with chloroform and water. The organic layer was dried over anhydrous Na2SO4 and concentrated by evaporation. After removing the solvent under reduced pressure, the residue was purified by recrystallization from acetone (800 mg, 69%). 1H NMR (600 MHz, CDCl3): 7.98\\u20137.96 (d, 2H), 7.84\\u20137.83 (d, 2H), 7.48 (s, 2H), 0.39 (s, 18H).\\nSynthesis of 2,7-bis(trimethylstannyl)naphtho[2,1-b:6,5-b\\u2032]dithiophene (TPA-NADT-TPA). Compound (5) (350 mg, 0.616 mmol) and compound (2) (640 mg, 0.166 mmol) were vacuumed for 20 minutes prior to adding anhydrous DMF (35 mL). The solution was degassed with argon for 20 minutes and then tetrakis(triphenylphosphine)palladium (25 mg, 0.022 mmol) was added. The reaction was refluxed at 110 \\u00b0C for 48 hours then extracted with chloroform. The extract was dried and concentrated. The purification of the residue on silica using hexane:dichloromethane (2:1 v/v) as the eluent. It was recrystallized from hot methanol to yield the desired compound as a yellow solid (200 mg, 38.4%). 1H NMR (600 MHz, CDCl3): \\u03b4 7.89\\u20137.88 (d, J = 8.4 Hz, 2H), 7.75\\u20137.74 (d, J = 8.4 Hz, 2H), 7.50\\u20137.43 (m, 6H), 7.02 (s, 8H), 6.88 (s, 4H), 6.79\\u20136.78 (d, J = 9.0 Hz, 8H), 3.74 (s, 12H). 13C NMR (120 MHz, CDCl3): \\u03b4 156.26, 149.30, 143.51, 140.27, 138.28, 137.38, 130.53, 126.97, 125.62, 122.35, 121.21, 120.35, 119.07, 118.18, 114.73, 55.52. ESI-MS: C54H42N2O4S2+\\u02d9 m/z 846.33 (calculated m/z 846.26).\\nSynthesis of 4,4\\u2032-(anthracene-2,6-diyl)bis(N,N-bis(4-methoxyphenyl)aniline) (TPA-ANR-TPA). In a round bottom flask, compound (5) (200 mg, 0.599 mmol), compound (4) (723 mg, 1.677 mmol), and 2 M aqueous K2CO3 solution (12 mL) were dissolved in anhydrous toluene (20 mL). The solution was degassed by argon for 20 minutes, and then tetrakis(triphenylphosphine)palladium (21 mg, 0.018 mmol) was added. Subsequently, the mixture was degassed for 30 min before the reaction was stirred at 120 \\u00b0C for 2 days. After the reaction mixture was cooled to room temperature and extracted with chloroform and water, the organic layer was dried over anhydrous Na2SO4. After removing the solvent under reduced pressure, the residue was purified using silica gel column chromatography with a mixture of hexane, chloroform, and ethyl acetate as the eluent. Then the crude product was recrystallized from hot methanol to yield the desired compound as a yellow solid (180 mg, 38.3%). 1H NMR (600 MHz, CDCl3): \\u03b4 8.33 (s, 2H), 8.05 (s, 2H), 7.96\\u20137.94 (d, J = 9 Hz, 2H), 7.66\\u20137.64 (dd, J = 1.8, 10.2 Hz, 2H), 7.53\\u20137.52 (d, J = 8.4 Hz, 4H), 7.05\\u20137.04 (d, J = 9 Hz, 8H), 6.98\\u20136.97 (d, J = 8.4 Hz, 4H), 6.80\\u20136.78 (m, 8H), 3.74 (s, 12H). 13C NMR (120 MHz, CDCl3): \\u03b4 155.96, 140.84, 137.18, 132.73, 131.97, 131.05, 128.53, 127.68, 126.69, 125.93, 125.37, 124.35, 120.78, 114.74, 55.52. ESI-MS: C54H44N2O4+\\u02d9 m/z 784.50 (calculated m/z 784.33).\\nSynthesis of 4,4\\u2032-(anthracene-2,6-diyl)bis(N,N-bis(4-methoxyphenyl)aniline) (DPA-ANR-DPA). Compound (6) (200 mg, 0.599 mmol), bis(4-methoxyphenyl)amine (343 mg, 1.497 mmol), and NaOtBu (149 mg, 1.797 mmol) were added and vacuumed for 30 min. Afterwards, anhydrous toluene (25 mL) and tBu3P (1 M toluene solution, 20 \\u03bcL, 0.02 mmol) were added to dissolve the solid and degassed by argon for 30 min. Then, Pd2(dba)3 (22.2 mg, 0.024 mmol) was added and the mixture was vacuumed and degassed for 30 min. Subsequently, the reaction was stirred at 110 \\u00b0C for 2 days. After the reaction mixture was cooled to room temperature and extracted with chloroform and water, the organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The residue was purified using silica gel column chromatography with a mixture of hexane and chloroform as the eluent. Then the crude product was recrystallized from hot methanol to yield the desired compound as a yellow solid (190 mg, 50.2%). 1H NMR (600 MHz, CDCl3): \\u03b4 7.94 (s, 2H), 7.69\\u20137.68 (d, J = 9, 2H), 7.25 (s, 2H), 7.19\\u20137.18 (dd, J = 1.8, 9 Hz, 2H), 7.13\\u20137.12 (d, J = 9 Hz, 8H), 6.88\\u20136.87 (d, J = 9 Hz, 8H), 6.80\\u20136.78 (m, 8H), 3.84 (s, 12H). 13C NMR (120 MHz, CDCl3): \\u03b4 155.81, 144.92, 141.11, 131.55, 128.98, 128.30, 126.84, 126.41, 123.69, 115.27, 114.67, 55.52. ESI-MS: C42H36N2O4+\\u02d9 m/z 632.42 (calculated m/z 632.27).\\n\\nOLED devices based on TPA-NADT-TPA, TPA-ANR-TPA and DPA-ANR-DPA were fabricated by thermal evaporation. The three synthesized materials were used as dopants with the device configuration of: ITO/HATCN (10 nm)/NPB (45 nm)/MADN: 3 wt% dopant (35 nm)/TPBi (35 nm)/LiF (1 nm)/Al (150 nm). In this configuration, 1,4,5,8,9,11-hexaazatriphenylene hexacarbonitrile (HATCN) and 4,4\\u2032-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPB) act as hole injecting and transporting layers, respectively. Additionally, while 2-methyl-9,10-bis(naphthalen-2-yl)anthracene (MADN) was used as the host compound, 1,3,5-tris(N-phenyl benzimidizol-2-yl)benzene (TPBi) was used as the electron-transporting layer. Furthermore, LiF and Al were used as the electron injecting layer and cathode, respectively. All organic and inorganic layers were deposited onto the UV ozone treated ITO glass substrates in a multiple thermal source vacuum deposition chamber at 2 \\u00d7 10\\u22126 Torr. The device electroluminescence performances such as current\\u2013voltage, brightness, electroluminescence spectra, and CIE co-ordinates were measured and recorded using a Spectra PR650 CCD camera with a computer-controlled DC power supply.\\n\\nPoly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS, AI 4083) and bathocuproine (BCP) were purchased from Heraeus and Lumtec, respectively. PbI2 was purchased from TCI (Tokyo Chemical Industry). Other chemicals were purchased from Sigma-Aldrich. PCBM (60) was purchased from Nano-C. Methylammonium iodide (MAI) was synthesized according to a previously reported method. The perovskite precursor solution (MAPbI3) was prepared by dissolving MAI and PbI2 at a stoichiometric ratio in gammabutyrolactone/dimethyl sulfoxide (7:3 v/v, 1.1 M) at 80 \\u00b0C.\\nPerovskite solar cells were prepared on a pre-cleaned patterned ITO substrate. A filtered PEDOT:PSS solution was spin-coated on ITO at 3000 rpm and annealed at 150 \\u00b0C for 10 min. For new HTM (TPA-NADT-TPA, TPA-ANR-TPA, and DPA-ANR-DPA) based devices, while TPA-ANR-TPA was prepared with a mixed solvent of chloroform and 1,2-dichlorobenzene at 2 mg mL\\u22121 (1:1 v/v), TPA-NADT-TPA and DPA-ANR-DPA were dissolved in 1,2-dichlorobenzene at 5 mg mL\\u22121. Afterwards, they were spin-coated on the ITO substrate. The film thickness was varied by changing the spin speed from 2000 rpm to 5000 rpm. The perovskite precursor solution (pre-heated at 80 \\u00b0C) was spin-coated onto these hole-transporting layers at 1000 rpm for 10 s and 4000 rpm for 30 s, and 250 \\u03bcL toluene was dripped on the sample surface at 15 s of the second step spin-coating. Subsequently, the perovskite layer was annealed at 80 \\u00b0C for 5 min and at 100 \\u00b0C for 30 min. The PCBM solution was coated from a chlorobenzene solution (20 mg mL\\u22121) at 1000 rpm for 60 s. The devices were completed by evaporating BCP (6 nm) and Ag (120 nm) sequentially under high vacuum (1\\u00d7 10\\u22126 mbar). The active area was 7 mm2 as defined by the overlapping between the back electrode and ITO. Current density\\u2013voltage (J\\u2013V) characteristics were measured using a calibrated solar simulator (AAA, SAN-EI ELECTRIC CO., LTD) coupled with a Keithley 2400 Source meter. External quantum efficiency (EQE) was obtained by combining a monochromatic light source, a light chopper and a lock-in amplifier (SR830-DSP).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80.0; 100.0,\\n Perovskite_deposition_thermal_annealing_time: 5.0; 30.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Indium tin oxide (ITO) glass substrate with a sheet resistance of 10 \\u03a9 sq\\u22121 was purchased from Nanbo Group (Shenzhen, China). Formamidinium iodide (FAI), methylammonium bromine (MABr), lead iodide (PbI2), lead bromide (PbBr2), Ca(acac)2, hydroiodic acid (HI, 57 wt% in H2O), dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF), and chlorobenzene (CB) were purchased from Sigma-Aldrich. PCBM was bought from Luminescence Technology Co., Ltd. Methylamine (CH3NH2, ca. 40% in water) was purchased from Tokyo Chemical Industry Co., Ltd.\\n\\nMethylamine (27.86 mL) and hydroiodic acid (30 mL) were mixed at 0 \\u00b0C and stirred for 2 h. The precipitate was recovered by evaporation at 50 \\u00b0C for 1 h. The product was washed with diethyl ether three times and finally dried at 60 \\u00b0C in a vacuum oven for 24 h.\\n\\nThe ITO-coated glass substrates were ultrasonicated in a solution consisting of detergent, deionized water, acetone, and isopropanol for 15 min, and subsequently dried in an oven overnight. For NiOx, nickel(II) acetate tetrahydrate (Sigma-Aldrich, \\u226599.0%, 50 mg mL\\u22121 in ethanol) was spin-coated onto the substrates at 4000 rpm for 45 s and annealed at 300 \\u00b0C for 1 h. For MAPbI3, the precursor solution was prepared by dissolving the mixture of PbI2 and CH3NH3I (1:1 in molar ratio) in a mixed solvent of DMF and DMSO (4:1 in volume ratio). For the mixed perovskite precursor, FA0.85MA0.15Pb(I0.85Br0.15)3 was prepared by dissolving 1.2 M metal lead salts consisting of 0.85 PbI2 and 0.15 PbBr2 and 1.2 M organic salts consisting of 0.85 FAI and 0.15 MABr in a co-solvent of DMSO/DMF (4:1, by volume). The perovskite precursor solution was then spin-coated onto the ITO/NiOx substrate at 1000 rpm for 10 s and 4000 rpm for 40 s. During the second spin-coating step, the substrate was treated with CB drop-casting. Then, the films were annealed at 100 \\u00b0C for 45 min. After they were cooled down to room temperature, PCBM (dissolved into chlorobenzene (CB), 20 mg mL\\u22121) was spun on top of the formed perovskite layers (for samples with a PCBM layer). After that, the films were annealed at 100 \\u00b0C for 10 min to enable the PCBM to crystalize and diffuse into the perovskite layer. The device was finished by spin coating a Ca(acac)2 solution with different concentrations. Finally, the device was transferred to a vacuum chamber (about 10\\u22125 Pa), and a Ag electrode (about 60 nm thick) was thermally deposited onto it.\\n\\nThe thicknesses of the perovskite films were examined by a film thickness measuring instrument (KLA Tencor D-120). The morphologies of the perovskite films were characterized by SEM (S4800, Hitachi, Japan). The transmittance and absorbance spectra were obtained by using a UV-vis spectrometer (PE Lambda 950 UV-vis spectrophotometer). The ultraviolet photoelectron spectroscopy (UPS) measurements were conducted in an ultra-high vacuum using a ULVAC-PHI ultraviolet photoelectron spectrometer equipped with a monochromatic He ultraviolet source HeI (h\\u03bd = 21.22 eV). The photocurrent\\u2013photovoltage (J\\u2013V) characteristics of the perovskite solar cells were measured by using a solar simulator (Newport, Oriel Class A, 91195A) with a source meter (Keithley 2450) at 100 mW cm\\u22122 illumination AM1.5G and a calibrated Si-reference cell certificated by NREL. The J\\u2013V curves of all devices were measured by masking the active area with a metal mask of 0.04 cm2 area. The external quantum efficiency (EQE) was measured by using a power source (Newport 300 W xenon lamp, 66920) with a monochromator (Newport Cornerstone 260) and a multimeter (Keithley 2001). The excitation and emission spectra were measured using a HORIBA Fluorolog-III spectrofluorometer (Lake Shore Cryotronics as the cryogenic refrigeration equipment).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Ca(acac)2,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Electrode preparations. Graphene oxide (GO) was prepared by the pre-oxidation of a natural graphite powder (<20 \\u03bcm, Sigma Aldrich) with a modified Hummers' method. Then, the as-prepared GO was placed into a horizontal tube furnace at 300 \\u00b0C for 5 min under a flow of 5% H2/Ar gas to produce reduced graphene oxide (RGO) powders. For the preparation of electrodes, the RGO powders (85 wt%, active material) were mixed with acetylene black (5 wt%, conductive agent) and poly(vinylidene fluoride) (10 wt%, PVDF, binder) in N-methyl-2-pyrrolidone (NMP) solvent. A slurry of the aforementioned mixture was ground using an agate mortar and pestle for 2 h and then cast onto carbon papers by a doctor-blade technique. After drying the electrode in an oven at 100 \\u00b0C for 1 h, it was thermally and mechanically pressed for 5 s at 10 MPA and 100 \\u00b0C.\\nPolymer electrolyte supercapacitors. The PVA/H3PO4 electrolyte was fabricated from an aqueous solution prepared by mixing a polyvinyl alcohol (50 wt%, PVA, Aldrich MW = 89000\\u201398000) with phosphoric acid (50 wt%, H3PO4, Aldrich). A thin layer of the PVA/H3PO4 was coated on the surface of the RGO electrode (PVA/RGO), followed by drying the PVA/RGO electrode in an oven at 100 \\u00b0C for 1 hour. The solid-state electrolyte electrochemical supercapacitors were assembled in a symmetric configuration using two pieces of PVA/RGO electrodes and a porous polypropylene separator (Celgard 3501). The as-assembled devices were finally pressed for 10 s under 2 MPa.\\n\\nMaterials. All materials, including PSS, PEI, reagents, and solvents, were purchased from Sigma-Aldrich unless otherwise stated. The PbI2 and CH3NH3I were purchased from Alfa Aesar and One Materials, respectively. The conjugated polymer PTB7-Th (10 mg, One Materials) and PC71BM (15 mg, Nano-C) were dissolved in 1 mL of CB:TCB (97:3, volume ratio). For the ZnO precursor solution, zinc acetate dehydrate (Zn(CH3COO2\\u00b7H2O), Sigma-Aldrich, 99.9%, 1 g) and ethanolamine (NH2CH2CH2OH, Sigma-Aldrich, 99.8%, 0.28 g) were dissolved in 2-methoxyethanol (CH3OCH3CH2OH, Sigma-Aldrich, 99.8%, 10 mL), and the solution was vigorously stirred in air for 12 h.\\nFabrication of polymer solar cells. Polymer solar cells were fabricated with a structure of ITO/ZnO/PTB7-Th:PC71BM/MoOx/Ag. Patterned ITO/glass substrates (15 \\u03a9 sq.\\u22121) were cleaned with detergent, ultrasonicated in acetone and isopropyl alcohol, and subsequently dried overnight in an oven. For the electron selective layer of the PSCs, a sol\\u2013gel ZnO precursor solution was spin-cast in air onto the pre-cleaned and UV/ozone-treated ITO/glass substrates at 5000 rpm for 30 s (\\u223c15 nm thickness). Then, the films were pre-heated on a hot plate at 200 \\u00b0C for 15 min. The substrate (ITO/ZnO) was transferred into a N2-filled glovebox, where a PTB7-Th:PC71BM solution was coated onto the ITO/ZnO substrate at 1000 rpm for 40 s. Finally, these samples were pumped down to a vacuum (1 \\u00d7 10\\u22127 torr; 1 torr \\u2248 133 Pa), and an approximately 5 nm-thick MoOx and 110 nm-thick Ag electrode (active area: 4.64 mm2) was deposited on top of the devices. The large-area (100 mm2) solar cells were fabricated similarly except for substrate and mask size.\\nFabrication of perovskite solar cells. For the PeSCs, the device structure was ITO/PSS/PTAA/perovskite/PC61BM/PEI/Ag. The PSS (Sigma Aldrich) was diluted to 0.25 wt% in DI-water and spin-coated onto a pre-cleaned ITO substrate at 5000 rpm for 20 s. After drying the ITO/PSS substrate at 150 \\u00b0C for 10 min, a PTAA solution (2.5 mg mL\\u22121 in toluene) was spin cast (at 6000 rpm for 40 s) on top of the ITO/PSS. The PTAA film was then annealed at 150 \\u00b0C for 10 min in air. The perovskite precursor solution (MAPbI3, 1.5 M in 1 mL of DMF:DMSO (8.5:1.5, volume ratio)) was spin cast (at 4000 rpm) onto the PTAA film, and diethyl ether (1 mL) was dropped on the perovskite precursor film after 10 s in the N2-filled glovebox. The precursor film was annealed on a hot plate at 100 \\u00b0C for 10 min. Then, a PC61BM solution (40 mg mL\\u22121 in chlorobenzene) was spin cast (at 1500 rpm for 40 s) onto the MAPbI3 film to form an approximately 100 nm-thick film. After spin-casting a PEI (0.25 wt%, IPA) onto the PC61BM at 5000 rpm, a 110 nm-thick Ag electrode was then successively deposited on top of the devices.\\nPhotovoltaic characterization. The J\\u2013V characteristics were measured using a Keithley 237 source measure unit in an N2 atmosphere. The solar\\u2013cell parameters were obtained using an AM 1.5 G solar simulator with an irradiation intensity of 100 mW cm\\u22122. The lamp was calibrated with an NREL-calibrated KG5 filtered silicon reference cell.\\nFabrication of integrated power packs. The power packs were fabricated by stacking the supercapacitor onto the large area solar cells. First, small amount of silver epoxy (MG chemicals, #8331) was put onto the middle surface of the Ag electrode of the solar devices. Then, the supercapacitor was carefully put down onto the below Ag electrode and attached to the solar cell by applying pressure (2646 Pa). Because the silver epoxy exhibits strong adhesion, high electric conductivity, and lack of chemical/mechanical damage to the underlying film, both the devices were successfully integrated. After then, the integrated power pack was encapsulated with a glass substrate by using transparent epoxy (Devcon 31345).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PEI,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"To prepare the perovskite precursor, commercial material powders, such as methylammonium iodide (MAI; Lumtec 99.99%, LT-S9126), lead(II) iodide (PbI2; Alfa Aesar 99.9985%), and lead(II) chloride (PbCl2; Alfa Aesar 99.999%, metals basis), were used without any further processing. Dimethylformamide (99.5%) and \\u03b3-butyrolactone (GBL; 99.5%) were used as main solvents, PCBM (Nano-C, 99.5%) was used as the ETL, and PEDOT:PSS (Clevious PVP AI 4083) was used as the HTL.\\nFor the preparation of the perovskite precursor, mixed halide perovskite (MAPbI3\\u2212xClx) with a material composition of MAI:PbCl2:PbI2 = 2:1:1 was used based on mixed solvents of composition DMF:GBL = 97:3 (v/v). Hydroiodic acid (HI, 57 wt% in H2O, distilled, stabilized, 99.95%; Sigma-Aldrich) of about 10 vol% of the main solvents was added to the perovskite precursor after overnight stirring at 65 \\u00b0C. CBZ was used in the washing treatment for the perovskite absorber layer. In addition, various PCBM solutions were made by mixing 1 \\u03bcL, 5 \\u03bcL, 10 \\u03bcL, 40 \\u03bcL, and 80 \\u03bcL of PCBM (2 wt% in CBZ) with 4 mL of CBZ, to create additional CBZ + PCBM solutions for the washing treatment. The CBZ + PCBM solutions were prepared as shown in Fig. 1(a). The PEDOT:PSS solution was used as is, and spin-coated after filtering through 0.45 \\u03bcm hydrophilic polytetrafluoroethylene (PTFE) for HTL coating. The PCBM ETL was made by preparing a solution of 20 mg of PCBM in 1 mL of CBZ.\\nFor the device fabrication process, Sn-doped In2O3 (ITO) glass substrates (15 \\u03a9 sq\\u22121) were ultrasonically cleaned with acetone (10 min), methyl alcohol (10 min), and IPA (10 min). After UV-ozone treatment (20 min), the PEDOT:PSS HTL was spin-casted on the ITO substrates at a spin-speed of 4000 rpm for 50 s, and the substrates were then annealed at 140 \\u00b0C for 20 min in atmospheric air. Then, MAPbI3\\u2212xClx perovskite films (\\u223c400 nm) were spin-coated at 5000 rpm as the absorber layer of the solar cells. Non-polar solvent washing with CBZ was carried out during spin-coating. The mixed CBZ + PCBM solutions were also used to quench the main solvent, DMF, in the perovskite films. The perovskite films were then annealed at 75 \\u00b0C for 60 min to further remove residual solvents. Next, PCBM ETL was spin-casted at 1500 rpm for 35 s, and device fabrication was completed by making aluminum (Al) electrodes using a thermal-evaporation system.\\nThe perovskite films treated with the CBZ + PCBM solutions were characterized using ultraviolet-visible (UV-Vis) spectrophotometry (UV-2700; Shimadzu) to check the variation in the absorbance of the MAPbI3\\u2212xClx mixed halide perovskite films. Structural properties of the perovskite films were measured and analyzed using X-ray diffraction (XRD) (R&D-100; Rigaku SmartLab). The surface morphologies of the films were investigated using field emission scanning electron microscopy (FE-SEM) (Ultra Plus; Zeiss) and atomic force microscopy (AFM) (SA-AFM; Proves Inc.). Also, energy dispersive spectroscopy (EDS) mapping and phase imaging techniques were also carried out to elucidate the PCBM location more directly. The film thicknesses were checked using a surface profiler (D-100; KLA Tencor). Additionally, we performed measurement of time-resolved photoluminescence (TRPL) of the perovskite films made with and without various PCBM contents (from 10 \\u03bcL to 80 \\u03bcL). Carrier lifetimes of the perovskite light harvesters were obtained by measuring high sensitivity spectrophotofluorometry with time correlated single photon counting (HORIBA SCIENTIFIC; Fluorolog3 with TCSPC) at room temperature. For excitation of carriers, a NanoLED (wavelength: 260 \\u00b1 10 nm, pulse width: <1.2 ns) with a typical power of 1\\u20132 pJ pulse\\u22121 was applied with a repetition rate of 1 MHz. A detector consisting of a single photon counting photomultiplier was employed for this TRPL measurement. The fabricated perovskite solar cells were characterized using a solar simulator (Polaronix K201; McScience) under AM 1.5 solar spectrum under standard conditions (100 mW cm\\u22122, 25 \\u00b0C) to evaluate current\\u2013voltage (J\\u2013V) properties.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl; HI,\\n Perovskite_deposition_solvents: DMF; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"For preparing the Cs0.15FA0.85PbI2.55Br0.45 precursor solution, 0.104 g CsBr, 0.600 g FAI, 1.600 g PbI2 and 0.184 g PbBr2 were dissolved together in a mixture of 0.280 mL of anhydrous DMSO and 1.930 mL of anhydrous DMF. For preparing the MAPbI3 precursor solution, 0.222 g of MAI and 0.461 g of PbI2 were dissolved together in a mixture of 0.800 mL of DMF and 0.200 mL of NMP. The precursor solutions were heated at 80 \\u00b0C for an hour and then filtered through a 0.45 \\u03bcm PTFE syringe filter.\\n\\nGlass/ITO substrates (Kintec, 15 \\u03a9 sq\\u22121) were sequentially cleaned with toluene, acetone, and isopropanol. Then the ITO slides were air-plasma treated for 5 minutes and immediately coated with a SnO2 layer by spin-coating a 10% aqueous tin dioxide suspension (Alfa-Aesar) at 4000 rpm for 40 s followed by annealing at 165 \\u00b0C in air for 15 minutes. All subsequent steps were performed under an inert atmosphere inside a nitrogen glove box. A solution of PCBM (15 mg mL\\u22121) was spin coated at 3000 rpm for 30 seconds. The perovskite precursor solutions (70 \\u03bcL) were spin coated at 4000 rpm and quenched with 130 \\u03bcL of toluene dropped 18 seconds later. The deposited films were annealed for 10 minutes at 100 \\u00b0C on a hotplate. Then a solution of 4 mg mL\\u22121 PTA or PTAA in toluene was spin-coated at 1000 rpm on top of the perovskite films. Molybdenum oxide (15 nm)/Ag (100 nm) electrodes were evaporated through a shadow mask. The device active area was 0.08 cm2 as defined by the shadow mask.\\nThe current\\u2013voltage characteristics of the devices were measured in an inert nitrogen atmosphere inside a glove box using simulated AM1.5G illumination (100 mW cm\\u22122) provided by a Newport VeraSol AAA class solar simulator. The intensity of the illumination was checked before each measurement using a calibrated silicon diode with a known spectral response. J\\u2013V curves were recorded using Advantest 6240A source-measurement units. EQE spectra were measured using a PV Instruments system integrated with an MBraun glove box.\\n\\nKelvin probe force microscopy measurements were performed in 2-pass amplitude modulation mode using a Cypher ES atomic force microscope installed in an Ar-filled MBraun glove box using conductive ASYELEC-01 probes. Atomic force microscopy measurements were performed in tapping mode using ASYELEC-01 probes. SEM images were obtained using a Zeiss SUPRA 25 instrument.\\n\\nCharge carrier mobilities were investigated using the space-charge limited current (SCLC) method. To perform the measurements, hole-only ITO/PEDOT:PSS (60 nm)/polymer/F4TCNQ (1 nm)/MoO3 (22 nm)/Ag (120 nm) devices were fabricated. The charge carrier mobilities were estimated using a standard approach utilizing the part of the current\\u2013voltage characteristic after the trap filling threshold.\\nCyclic voltammetry measurements were performed for thin films (150\\u2013250 nm thick) of the polymers PTA and PTAA deposited on a glassy carbon disc electrode (working electrode, d = 5 mm, BAS Inc.) by drop-casting from chlorobenzene. The measurements were performed in a three-electrode electrochemical cell using a 0.1 M solution of Bu4NPF6 in acetonitrile as the supporting electrolyte, a platinum wire as the counter electrode, and a silver wire immersed in a 0.01 M solution of AgNO3 in 0.1 M TBAP (CH3CN) as the reference Ag/Ag+ electrode (BAS Inc.). Ferrocene was used as the internal reference. The electrolyte solution was purged with argon before the measurements. The voltammograms were recorded using an ELINS P-30SM instrument at room temperature with a potential sweep rate of 50 mV s\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs0.15FA0.85PbBr0.45I2.55,\\n Perovskite_composition_short_form: CsFAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FAI was synthesized as previously reported. Briefly, by reacting formamidine acetate with 2\\u00d7 molar excess of hydroiodic acid (45 wt% in water) in a 250 mL round-bottomed flask at 50 \\u00b0C for 10 min with stirring. A yellowish raw precipitate was formed after rotary evaporation at 50 \\u00b0C. The precipitate was washed with diethyl ether and recrystallized twice with a mixed solvent of ethanol and diethyl ether to form white needle-like crystals. Then it was dried at 60 \\u00b0C in a vacuum oven for 12 h. PEDOT:PSS (Clevious PVP Al4083), PbI2 and PCBM were purchased from H. C. Starck, Aladdin reagent and American Dye Sources, respectively. All of the materials were used as received unless specially emphasized. ITO glass substrates with a sheet resistance of 15 \\u03a9 sq\\u22121 were purchased from Shenzhen Display.\\n\\nA concentration of 1.0 M perovskite precursor solution was prepared by dissolving FAI with an equal molar ratio of PbI2 in a mixed solvent of \\u03b3-butyrolactone (GBL) and dimethyl sulfoxide (DMSO) (GBL:DMSO = 7:3), stirring overnight before use. FAI/IPA solution was prepared by dissolving FAI into anhydrous IPA with an optimized concentration of 2 mg mL\\u22121. The ITO coated glass substrates were precleaned sequentially in detergent, deionized water, acetone, and isopropyl alcohol and then treated in oxygen plasma. The PEDOT:PSS (Clevious AI 4083) layer (30 nm) was coated by spin-coating at 4000 rpm for 20 s, and annealed at 150 \\u00b0C for 20 min in air. The precursor solution was spin coated on the PEDOT:PSS layer using a fast deposition crystallization procedure in a nitrogen filled glovebox. The precursor solution was spin-coated at 4000 rpm or 6000 rpm to control its thickness. Then, the FAPbI3 coated substrate was put on a hot plate and annealed at 150 \\u00b0C for 10 min, the modification procedure of FAPbI3 film was performed by spin coating FAI/IPA solution on the film surface at 4000 rpm. Samples were annealed at 150 \\u00b0C for 20 min. After cooling down to room temperature, 40 nm thick PCBM (15 mg mL\\u22121 in chlorobenzene) was spin-coated on the perovskite layer. Finally, the films were transferred into a thermal evaporation system for Al cathode evaporation. The active area is 0.1 cm2 defined by the shadow mask. FAPbI3 based solar cells without FAI/IPA modification were also fabricated for comparison.\\n\\nFilm thicknesses were measured using a Veeco Dektak 150 surface profiler. X-ray diffraction (XRD) patterns were obtained from a Bruker D8 ADVANCE. Ultraviolet-visible spectroscopy (UV-vis) was performed from 450 to 850 nm via Hitachi U-4100. A scanning electron microscope (SEM, Hitachi S-4800) was used for surface morphology characterization. Current density\\u2013voltage (J\\u2013V) characteristics of the devices were measured in a N2-filled glovebox with a Keithley 2420 source measurement under AM1.5G, 100 mW cm\\u22122 (Newport). The light intensity was calibrated using a standard silicon solar cell. The J\\u2013V curves were obtained via reverse scan (from bias 1.2 V to \\u22120.1 V) and the scan rate was 0.1 V s\\u22121. The external quantum efficiency (EQE) of the solar cell was analysed using a certified Newport incident photon conversion efficiency (IPCE) measurement system. Steady-state photoluminescence (PL) spectra were recorded on a Fluoromax 4 spectrometer (HORIBA Jobin Yvon) with a photoexcitation at 680 nm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL @ 3; 7 >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150.0 >> 150.0,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> 20.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Aqueous dispersion of PEDOT:PSS (1.3\\u20131.7 wt%, from H.C. Stark Baytron P AI 4083) was obtained from Heraeus Co. Fullerene derivatives (PC71BM (99.58%) and ICBA (99.5%)) was purchased from Solenne B. V., Netherlands. PbBr2 (99.999%) was obtained from Aldrich. All the above materials were used as received. ITO-covered glass substrates purchased from Ruilong Co., Taiwan were photolithographically patterned in our laboratory with HCl(aq). CH3NH3Br (MABr) was synthesized as reported previously. Uv/Vis absorption and PL spectra were recorded with Hitachi U-4100 and F-7000 spectrometers, respectively. The thickness of the films was measured with a depth-profile meter (Veeco Dektak 150, USA). Five lines on the 1 cm \\u00d7 1 cm film were made by carefully scratching with a tip and the average height between the hills and valleys was used to represent the film thickness. GIXRD data were collected in the 2\\u03b8 range of 10\\u201350 degrees on a Bruker powder diffractometer (D8 Discover) using Cu K\\u03b11 radiation equipped with a 2D detector. Scanning Electron Micrograph (SEM) and Energy Dispersive Spectroscopy (EDS) were performed with a Hitachi S-800 microscopy at 15 KV. Samples (film on substrates) for SEM imaging and EDS study were mounted on a metal stub with a piece of conducting tape and then coated with a thin layer of gold film to avoid charging. Time-resolved photoluminescence (TR-PL) spectra were recorded by the time-correlated single-photon counting (TCSPC) technique (UniRAM, Protrustech) along with the instrument response function of 200 ps and the excitation wavelength (repetition rate) was 405 nm (20 MHz). To prevent laser-induced thermal effects, the diameter of the spot size on the sample was increased to 50 \\u03bcm and the excitation power was reduced to 0.1 mW. Depth profile X-ray photoelectron spectra were obtained with a Perkin-Elmer PHI-590AM XPS/ESCA spectrometer system with a Cylindrical Mirror Electron (CMA) energy analyser. The X-ray sources were Al K\\u03b1 at 600 W and Mg K\\u03b1 at 400 W. XPS were obtained at pass energies of 160 eV and 10 eV for survey scans and high-resolution scans, respectively. The sputtering time for each layer is 200 seconds.\\n\\nThe procedure for fabricating the solar cells reported in this paper is very similar to that for preparing CH3NH3PbI3 based devices we reported previously. PEDOT:PSS was spin-coated on a heat pretreated patterned ITO under 5000 rpm for 50 s and then annealed at 100 \\u00b0C for 15 min. To deposit the perovskite layer, first a layer of PbBr2 was spin-coated on top of the PEDOT:PSS-coated ITO substrate from 0.5 M DMF solution using a spin rate of 2000 rpm for 30 seconds. And then CH3NH3Br (MABr) was spin-coated on top of the PbBr2 film from its isopropanol solution (with various concentrations, volumes and spin programs) to form a CH3NH3PbBr3 structure. Specifically, the highest efficiency device was fabricated with a concentration of CH3NH3Br/isopropanol (IPA) ca. 15 mg mL\\u22121 (30 \\u03bcl) at a spin rate of 2000 rpm for 30 s in a 1.5 cm \\u00d7 1.5 cm substrate. After the CH3NH3PbBr3 film was formed, 24 wt% PCBM (or ICBA) in chlorobenzene was spin-coated onto the surface of the perovskite layer at 1000 rpm, 30 s to be an acceptor layer. All the fabrication procedures were carried out under ambient atmosphere at room temperature. Solvent annealing of the active (donor/acceptor) layer was carried out by covering the PEDOT:PSS/CH3NH3PbBr3/PCBM (or ICBA) film with a petri dish for 24 hours in a glove box before the film was sent into the vacuum evaporator for depositing an electrode. Finally the PEDOT:PSS/CH3NH3PbBr3/PCBM (or ICBA) film was transferred to a vacuum chamber to coat the Ca/Al (20 nm/100 nm) electrode using thermal evaporation. The device area is 0.5 cm \\u00d7 0.2 cm. I\\u2013V curves of the cells were obtained using a Keithley 4200 source measuring unit under a simulated AM1.5G sun light (Wacom solar simulator) at 100 mW cm\\u22122 and the light intensity was calibrated using a KG-5 Si diode. External quantum efficiency (EQE) or incident photo-to-current conversion efficiency (IPCE) was measured in air when the device was sealed with a three-bond sealer and measured right after taking out of the glove box. A chopper and lock-in amplifier were used for the phase sensitive detection with a QE-R3011 measurement system (Enlitech Co., Taiwan). The cell for the stability test outside the glove box was fabricated using the same procedures except Ag, instead of Ca/Al, was used as an electrode.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbBr3,\\n Perovskite_composition_short_form: MAPbBr,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ca | Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Graphene oxides (GOs) were prepared via the previously reported method. For the reduction process, the resulting GOs were dispersed in 100 ml of deionized (DI) water by using an ultrasonic bath with a concentration of 4 mg ml\\u22121. Then 2 ml of reductant (4-(trifluoromethyl)phenyl hydrazine, Sigma-Aldrich) was added into the GO colloidal solution, and stirred for 6 h. Subsequently, the colloidal solution was filtered by using a vacuum filter, and then, washed with alcohol. The filtered materials were dried in an oven at 60 \\u00b0C. Finally, the FrGO was dispersed in 2-propanol at a concentration of 1 mg ml\\u22121 for device-fabrication.\\n\\nThe configuration of the PeSCs studied in this report was ITO/ZnO/C60/MAPbI3/PEDOT/FrGO/MoO3/Ag. The pre-patterned ITOs (10 Ohm sq\\u22121, Samsung Corning) on glass-substrates were sequentially cleaned with acetone, deionized water, and 2-propanol in an ultrasonic bath for 20 min, respectively, and dried in an oven at 80 \\u00b0C for 10 min. Then, the substrates were exposed in the UV-ozone for 30 min. For the ZnO layer, zinc oxide nanopowder (ZnO nanopowder, <100 nm particle size, Sigma-Aldrich) dissolved in ammonium hydroxide solution (NH4OH, 50% v/v aq. soln, Alfa Aesar) at a concentration of 8 mg ml\\u22121 was spin-coated on the ITO-coated glass at 5000 rpm for 40 s, and subsequently dried at 200 \\u00b0C for 20 min in air. Then, C60 (fullerene, 99.5%, Nano-C) dissolved in 1,2-dichlorobenzene (15 mg ml\\u22121) was spin-coated on the ITO/ZnO substrates at 2000 rpm for 40 s, and annealed at 100 \\u00b0C for 10 min in an N2 glove box. Next, for the perovskite layer, PbI2 (lead(II) iodide, 99.9985%, Alfa Aesar) of 0.759 g and MAI (Dyesol) of 0.262 g were dissolved in DMF (anhydrous 99.8%, Sigma-Aldrich) solvent of 1.612 ml, and then, 120 ml of N-cyclohexyl-2-pyrrolidone (CHP, Sigma-Aldrich) was added into the solution. The prepared perovskite precursor solution was spin-coated on the ZnO/C60 at 4000 rpm for 40 s, followed by annealing at 100 \\u00b0C for 4 min in an N2 glove box. For the HTLs, PEDOT (Clevios HTL Solar 3) and FrGO solutions were spin-coated on the active-layer at 5000 rpm for 40 s, and then dried at 100 \\u00b0C for 5 min in an N2 glove box, respectively. Finally, the MoO3 (2.5 nm)/Ag (80 nm) electrodes were deposited via a thermal evaporator with a shadow mask to define an active-area of 4.64 mm2.\\n\\nThe photocurrent density\\u2013voltage (J\\u2013V) characteristics were measured by Keithley 2400 source measurement under AM 1.5 G illumination (100 mW cm\\u22122) using a solar simulator. Both external and internal quantum efficiency (EQE and IQE) of PeSCs were analyzed using a certified IPCE measurement system (IQE-200, Oriel Instruments). The integrated values of the JSC obtained from the IPCE data are in close agreement (within nearly 9%) with the values obtained from the J\\u2013V curves. To analyze interface characteristics, the impedance measurements of PeSCs were performed under white light conditions by using a Solartron 1260 Impedance/gain-phase analyzer, with a frequency range of 100000 Hz to 0.1 Hz and an AC oscillating voltage of 0.90 V. A Scribner ZView 2 software was used as the fitting program of the spectra. X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS) (AXIS-NOVA, Kratos Inc.) were carried out with monochromatic Al-K\\u03b1 (1486.6 eV) for XPS and He 1 (h\\u03bd = 21.2 eV) for UPS. The surface morphology and surface potential of the HTLs were detected by atomic force microscopy (AFM) and scanning Kelvin probe microscopy (SKPM) (Dimension 3100, Veeco), respectively. In order to compare optical transmittance according to spin-coating cycles of FrGO solution, UV-vis (LAMBDA 750 UV/Vis/NIR spectrophotometer, PerkinElmer Inc.) was used. The contact-angles of water-droplets on the HTLs were measured by Phoenix 300 (SEO Inc.). Scanning electron microscopy (SEM, Quanta 3D-FEG/FEI) was used to obtain the cross-sectional image of the PeSCs.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-np | C60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 4,\\n HTL_stack_sequence: PEDOT:PSS | FrGO,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 4.64,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned ITO-coated glass substrates with a sheet resistance of 15 ohm sq\\u22121 were purchased from Ruilong Tech. PEDOT:PSS aqueous solution (CLEVIOS P VP Al 4083) was purchased from Heraeus. Methylammonium iodide (MAI; >99.5%) and formamidinium iodide (FAI; >99.5%) were purchased from Lumtec. PC61BM (>99.5%) was purchased from Solenne. For preparation of the lead iodide (PbI2) complex, 25 g PbI2 was dissolved in anhydrous dimethylsulfoxide of 75 mL and toluene of 200 ml was then slowly added into the PbI2 solution. The white precipitate was then filtered and dried in a vacuum oven at 60 \\u00b0C for 12 h. Unless otherwise stated, all chemicals were purchased from Sigma-Aldrich and used as received.\\n\\nZnO NPs were synthesized by a solution\\u2013precipitation process according to literature procedures. Briefly, zinc acetate dihydrate (2.95 g) was dissolved in methanol (125 mL) at room temperature. A potassium hydroxide solution (1.48 g in 65 mL methanol) was then added dropwise within 30 min and stirred for 3 h at 65 \\u00b0C. The cooled-down solution was then decanted and the precipitate was washed twice with ethyl acetate and ethanol. Afterward, ethanol was added to disperse the precipitates and produce ZnO NP solution.\\n\\nITO-coated glass substrates were cleaned stepwise in detergent, water, acetone, and isopropyl alcohol under ultra-sonication for 20 min each and subsequently pretreated by UV-ozone for 60 min. The PEDOT:PSS layer (25 nm) was spin-coated on the ITO surface and then annealed at 120 \\u00b0C for 15 min. The MAPbI3 perovskite layer (\\u223c250 nm) was prepared following two-step solution deposition, as described in our previous work. Briefly, PbI2 and MAI were dissolved into anhydrous dimethylformamide (DMF) and anhydrous 2-propanol with concentrations of 450 mg mL\\u22121 for PbI2 and 40 mg mL\\u22121 for MAI, respectively. Both solutions and substrates were heated at 100 \\u00b0C for 10 min before being used. The PbI2 solution was spun on the preheated substrate (5000 rpm for 40 s) and then annealed at 70 \\u00b0C for 10 min. The MAI solution was then spun on top of the dried PbI2 film (6000 rpm for 30 s), followed by annealing at 100 \\u00b0C for 2 h. The FAPbI3 perovskite layer (\\u223c380 nm) was prepared according to the reported procedure. Briefly, the PbI2 complex solution (1.3 M in anhydrous DMF) was spun on the substrate (3000 rpm for 30 s). The FAI solution (0.465 M in anhydrous 2-propanol) was then spun on top of the dried PbI2 complex film (5000 rpm for 30 s), followed by annealing at 150 \\u00b0C for 10 min. Afterward, a solution consisting of 20 mg mL\\u22121 PC61BM with different doping ratios of CTAB in anhydrous chloroform was then spin-coated on top of the formed perovskite layers. The optimum thickness of the PC61BM layer for MaPbI3 and FAPbI3 was 60 and 80 nm, respectively. The opaque Ag (150 nm) was then deposited from a thermal evaporator under high vacuum (<10\\u22126 torr). Contributions to the Jsc from regions outside the active area were eliminated using illumination masks with an aperture size of 0.12 cm2 or 1.2 cm2.\\n\\nThe current\\u2013voltage characteristics of the as-fabricated solar cells were measured under ambient conditions using a Keithley 2400 source measurement unit. Unless otherwise stated, the scan rate was set at 0.15 V s\\u22121. An Oriel xenon lamp (450 Watt) with an AM1.5 G filter was used as the solar simulator. A Hamamatsu silicon solar cell (S1133) with a KG5 color filter, which is traced to the National Renewable Energy Laboratory (NREL), was used as the reference cell. To calibrate the light intensity of the solar simulator, the power of the xenon lamp was adjusted to make the Jsc of the reference cell under simulated sun light as high as it was under the calibration conditions. IPCE spectra were measured using a lock-in amplifier with a current preamplifier under short-circuit conditions with illumination of monochromatic light from a 250 W quartz-halogen lamp (Osram) passing through a mono-chromator. The work functions of the electrodes were measured with a ULVAC-PHI PHI 5000 Versaprobe II X-ray photoelectron spectrometer employing a mono-chromatic focused Al-K\\u03b1 X-ray source and hemispherical analyzer. The EPR spectra were obtained at room temperature using a Bruker ELEXSYS E-580 EPR spectrometer. Sample solutions were added to EPR test tubes and then degassed with nitrogen to form films on the tube walls at room temperature under a nitrogen atmosphere. Steady-state PL spectra were measured at room temperature by using a fluorescent spectrophotometer (Hitachi F-4600) with a 150 W Xe lamp as an excitation source at 600 nm. Time-resolved PL decay spectra were recorded by using a time-correlated single-photon counting system (Edinburgh Instruments FL920), and the excitation light pulse was provided using a picosecond diode laser at a wavelength of 450 nm, and the signal was monitored at \\u223c770 nm. The PL lifetimes of the samples were calculated by fitting the experimental decay transient data to the single-exponential decay model. The surface morphology of the films was studied using the tapping mode AFM from Digital Instrument D3100CL. The electrical conductivities of the thin films were measured by using a four point probe setup with a source measurement unit (Keithley 2400).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | ZnO-np,\\n ETL_additives_compounds: CTAB | Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 150.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals and reagents were used as received from chemical companies, including PbI2 (>98%, TCI), PbBr2 (99%, Sigma-Aldrich), HI (48% in water, Sigma-Aldrich), HBr (48% in water, Sigma-Aldrich), CH3NH2 (33 wt% in absolute ethanol, Sigma-Aldrich), formamidine acetate (99%, Sigma-Aldrich), titanium diisopropoxide bis(acetylactonate) 75% in isopropanol (Tiacac, Sigma-Aldrich), mesoporous-TiO2 paste (18NR-T, Dyesol), 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4TCNQ, 97%, Sigma-Aldrich), poly[2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b\\u2032]dithiophene)-alt-4,7(2,1,3-benzothiadiazole)] (PCPDTBT, average Mw 7000\\u201320000, Sigma-Aldrich).\\nThe NH = CHNH3I (FAI) and CH3NH3Br (MABr) were synthesized by the same methods according to a previously literature. The mixed-ion perovskite precursor solution (1.35 M) of (FAPbI3)1\\u2212x(MAPbBr3)x (x = 0.15) was prepared in a glovebox, by dissolving the FAI (1 M), MABr (0.2 M), PbI2 (1.1 M) and PbBr2 (0.2 M) in a mixed solvent of dimethyl formamide (DMF) and dimethyl sulfoxide (DMSO) (4:1, v/v), as reported previously.\\n\\nThe PSC devices were fabricated as described previously. Fluorine-doped tin oxide (FTO)-coated glass (Pilkington TEC 15) was firstly patterned by etching with Zn powder and HCl (2 M). The etched substrate was then sequentially cleaned by using detergent, de-ionized water, acetone and ethanol in ultrasonic bath. Remaining organic residues were removed under oxygen plasma for 30 min. A compact TiO2 blocking layer (BL) of roughly 30\\u201340 nm was deposited on the cleaned FTO glasses by spray pyrolysis of titanium diisopropoxide bis(acetylacetonate) diluted in anhydrous ethanol at a volumetric ratio of 1:10 and then heated at 500 \\u00b0C for 30 min. A mesoporous TiO2 layer was deposited by spin-coating TiO2 paste (Dyesol 18NR-T) diluted in anhydrous ethanol at ratio of 1:5 by weight at 5000 rpm for 30 s. The layers were then sintered in air at 500 \\u00b0C for 30 min. The mixed-ion perovskite films were deposited onto the mesoporous TiO2/BL TiO2/FTO substrates from the precursor solution by a two-step spin-coating procedure, at 1000 rpm for 10 s and then 5000 rpm for 30 s. During the second step, 200 \\u03bcL of chlorobenzene was dropped onto the substrates 10 s prior to the end of the program. The substrates were directly heated on a hotplate at 100 \\u00b0C for 60 min. After cooling to room temperature, different doping level of PCPDTBT:F4TCNQ composites HTMs were deposited on the perovskite layers at 2000 rpm for 30 s via solution process. 20 mg ml\\u22121 PCPDTBT solution was prepared by dissolving 20 mg PCPDTBT in 1 ml ortho-dichlorobenzene (DCB), stirred at 70 \\u00b0C for 30 min. P-type doping material F4TCNQ in DCB solution with a concentration of 2 mg ml\\u22121 was also stirred at 70 \\u00b0C for 30 min before adding to the PCPDTBT solution. After spin coating of the HTM layers, the substrates were heated at 65 \\u00b0C for 15 min. Finally, a layer of 100 nm Au was deposited on top of the HTM layers under high vacuum (<4 \\u00d7 10\\u22124 Pa) by thermal evaporation.\\nThe photocurrent\\u2013voltage (J\\u2013V) characteristics of the solar cells were measured using a Keithley 2400 Source-measure unit under illumination of a simulated sunlight (AM 1.5G, 100 mW cm\\u22122) provided by an Oriel Sol3A solar simulator (Newport USA, Model: 94023A) with an AM 1.5 filter in ambient air. Light intensity was calibrated with a Newport calibrated standard Si reference cell (SER. No: 506/0358). A black mask with a circular aperture (0.09 cm2) smaller than the active area of the square solar cell (0.20 cm2) was applied on top of the cell. The J\\u2013V curves were obtained from forward bias to short-circuit at a scan rate of 10 mV S\\u22121. The incident photo-to-current conversion efficiency (IPCE) was obtained by a Hypermono-light (SM-25, Jasco Co. Ltd., Japan). Prior to measurement, a standard silicon solar cell was used as reference.\\n\\nThe UV-vis spectra were obtained by Agilent 8453 spectrophotometer (Model: HP 8435, China). The infrared spectra were measured by Fourier Transform Infrared Spectrometer (FTIR) mode on 6700 (ThermoFisher, USA). The top view and cross-section scanning electron microscopy (SEM) images were obtained by HR-SEM performed with FEI (Field Emission Instruments: Nova Nano SEM 450), the USA. Conductivity measurements were performed as follows. Glass substrates were sequentially cleaned by detergent, de-ionised water, acetone and ethanol. Remaining organic residues were removed under oxygen plasma for 30 min. A thin layer of compact TiO2 (\\u223c30 nm) was coated on the glass substrates by spray pyrolysis. After sintering the TiO2 film at 500 \\u00b0C for 30 min, the film was cooled to room temperature. A solution of HTM in DCB was spin-coated onto the TiO2 substrate, whereas the concentration was the same as in case for the photovoltaic device. Finally, a 200 nm-thick of Ag was deposited on the top of the HTM by thermal evaporation under high vacuum (<4 \\u00d7 10\\u22124 Pa). A two-point probe setup was used with a keithley 2400 source meter for measuring linear current\\u2013voltage curves. Steady-state photoluminescence (PL) measurements were performed with spectrofluorometer (Horiba Jobin Yvon, Fluorolog-3) at excitation wavelength of 600 nm. Time-resolved photoluminescence was measured by use of time-correlated single photon counting (TCSPC) technique (PicoHarp 300, PicoQuant). For excitation, the second harmonic of femtosecond titanium-sapphire laser (Mai Tai DeepSee, Spectra Physics) at 425 nm (150 fs, 80 MHz) was utilized. For TCSPC measurements, the instrument response function is about 40 ps. Deconvolution/fitting procedure was performed by use of commercial software FluoFit Pro (PicoQuant); overall time resolution of the setup is 8\\u201310 ps. All measurements were done at room temperature. The HOMO energy level of the PCPDTBT film was examined using ultraviolet photoelectron spectroscopy (UPS) with photon energy of 40.8 V. A sample bias of 5.0 V was applied to observe the secondary electron cutoff. The electrochemical impedance spectroscopy (EIS) measurements were carried out at different applied bias in the dark condition using an impedance/gain-phase analyser (Zahner Model: Zennium, Serial No. 40037, German) electrochemical workstation with the scanning frequency range from 106 to 0.1 Hz. The magnitude of the alternative signal was 10 mV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: PCPDTBT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Inverted organic\\u2013inorganic perovskite solar cells with a structure of FTO/NiOx/CH3NH3PbI3/PCBM/BCP/Ag were made on prepatterned FTO substrates which were cleaned by sonication in a washing agent, acetone and isopropyl alcohol (IPA) for 20 minutes sequentially. Nickel(II) nitrate hexahydrate (Ni(NO3)2\\u00b76H2O) (Sigma Aldrich) was dissolved in ethylene glycol solution containing 1 M nickel nitrate hexahydrate and ethylenediamine (Sigma Aldrich). The resulting solution was filtered through a nylon membrane (0.22 \\u00b5m). The as-prepared NiOx solution was spin-coated onto the glass/FTO surface at a spin speed ranging from 2000 to 4000 rpm for 60 s and then annealed at 300 \\u00b0C in air for 120 minutes. The substrate was then transferred into a nitrogen-filled glove box for coating of the perovskite layer, where a one-step spin-coating process was adopted. 159 mg CH3NH3I (Dyesol Pte Ltd) and 461 mg PbI2 (Tokyo Chemical Industry Co., Ltd) were dissolved into a mixed solvent of 800 ml dimethylformamide (DMF) and 200 ml dimethyl sulfoxide (DMSO). For precursors with excess MAI, a small amount of MAI-containing solution was added to the stoichiometric precursor. The spin-coating procedure for perovskite films was performed at a changing speed: 2000 rpm for 10 s and then 5000 rpm for 30 s. Chlorobenzene (200 \\u00b5l) was dripped on the substrate very quickly during the second spin coating step 9 s before the end of the procedure. The substrate was then heated at 50 \\u00b0C for 5 minutes and then 100 \\u00b0C for 10 minutes on a hotplate. After cooling down to room temperature, a 1.77 wt% PC60BM (Nano-C) solution in chlorobenzene was subsequently spin-cast on top of the perovskite layer at 1000 rpm for 90 s. Finally, 8 nm of BCP and 70 nm of silver were deposited by thermal evaporation using a shallow mask to pattern the electrodes in a high vacuum system. The device area was defined as 0.0706 cm2 by using a mask during the measurements. Devices were encapsulated with cover glasses and UV-curable epoxy in a glove box.\\n\\nCurrent\\u2013voltage characteristics were recorded by applying an external potential bias to the cells in ambient air while recording the generated photocurrent or the injected dark current with a digital source meter (Keithley model 2400). The light source (SAN-EI XES-301S, AAA) was a 300 W xenon lamp equipped with a sunlight filter to match the emission spectrum of the lamp with the AM 1.5 G standard. The light intensity was varied using neutral density filters. A field emission scanning electron microscope (FESEM 7600F) was used to acquire high resolution SEM images with an accelerating voltage of 5 kV. The absorption spectra were obtained using a UV-vis-NIR Cary 5000. The time-resolved photoluminescence spectra were recorded using a time correlated single photon counting (TCSPC) fluorometer (DeltaFlex). Admittance spectra were measured by using an Agilent B1500 meter with an alternating voltage of 50 mV. The frequency-dependence of the capacitance was recorded from 1 kHz to 1 MHz with zero bias in the dark. The dependence of the capacitance on voltage was measured from \\u22120.5 to 2 V with a frequency of 1 kHz in the dark.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0706,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Synthesis of MAI. CH3NH3I was synthesized by stirring methylamine (CH3NH2) (33 wt% in absolute ethanol, Sigma Aldrich) with hydroiodic acid (57 wt% in water, Aldrich) in a round-bottom flask at 0 \\u00b0C for 2 hours. The solution was concentrated to dryness in the vacuum of the rotary evaporator. Methylammonium iodide (CH3NH3I) was washed carefully with diethyl ether and then recrystallized from a diethyl ether\\u2013ethanol mixture and dried at 60 \\u00b0C in a vacuum oven overnight.\\nSynthesis of HAI. Hydrazinium iodide (N2H5I) was synthesized by stirring hydrazine hydrate (\\u223c98%, Sigma Aldrich) and hydroiodic acid (57 wt% in water, Aldrich) in a round-bottom flask at 0 \\u00b0C. The isolation and purification of HAI was performed in a similar way as for MAI.\\nPreparation of MA1\\u2212xHAxPbI3 precursor solution. Lead iodide PbI2 (578 mg, 1.25 mmol) and methylammonium iodide MAI (200 mg, 1.25 mmol) were dissolved in 1 mL of dimethylformamide (DMF) to obtain the precursor solution I. PbI2 (578 mg, 1.25 mmol) and hydrazinium iodide HAI (201 mg, 1.25 mmol) were then dissolved in 1 mL of DMF to obtain the precursor solution II. Both solutions were stirred overnight at 70 \\u00b0C. Afterwards, precursor solutions I and II were mixed in the volume ratios of 0.5:9.5, 1:9, 2:8, 3:7, 4:6, 5:5, 6:4, and 8:2 to obtain a series of MA1\\u2212xHAxPbI3 precursor solutions.\\n\\nThe absorption spectra were obtained using an AvaSpec-2048-2 UV-VIS fiber spectrometer integrated inside the glove box.\\nScanning electron microscopy images were obtained on a Zeiss SUPRA 25 instrument. The samples were prefixed on a microscope stage inside the glove box to reduce the exposure time in air down to \\u223c1 min.\\nGIWAXS measurements of thin films were performed using a XeuSS SAXS/WAXS (Xenocs, France) machine coupled to a GeniX3D generator (\\u03bb = 1.54 \\u00c5). The 2D data were collected with an incidence angle of 0.2\\u00b0 using a Rayonix LX170-HS detector with a sample to detector distance of 16 cm. The modulus of the scattering vector s (s = 2sin\\u03b8/\\u03bb, where \\u03b8 is the Bragg angle) was calibrated using several diffraction orders of silver behenate powder.\\n\\nGlass/ITO substrates (5 \\u03a9/\\u25a1, Luminescence Technology Corp.) were sequentially cleaned with toluene and acetone and sonicated in deionized water, acetone and isopropanol. PEDOT:PSS (Clevios PH) was filtered through a 0.45 mm PES filter and spin-coated onto ITO slides at 3000 rpm. The resulting PEDOT:PSS films were then dried at 165 \\u00b0C for 15 min in air. The MA1\\u2212xHAxPbI3 precursor solutions were spin-coated at 5000 rpm inside a nitrogen glove box. Toluene (200 \\u03bcL) was dropped on the film 4\\u20135 s after the initiation of spin-coating, inducing film crystallization. Spinning was continued for 45 s and then the deposited films were annealed at 100 \\u00b0C for 15 min on a hotplate installed inside the glove box. A 30 mg mL\\u22121 solution of PCBM in chlorobenzene was spin-coated at 1500 rpm on the top of the MA1\\u2212xHAxPbI3 films prepared as described above. Silver electrodes (100 nm) were deposited through thermal evaporation in high vacuum (10\\u22126 mbar). The device active area was 0.5 cm2 as defined by a shadow mask. All steps of the device fabrication procedure following the annealing of the PEDOT:PSS films in air were carried out under an inert atmosphere inside the nitrogen glove box.\\nThe current\\u2013voltage (J\\u2013V) characteristics of the devices were obtained under an inert atmosphere using the simulated 100 mW cm\\u22122 AM1.5 solar irradiation provided by a KHS Steuernagel solar simulator integrated with a MBraun glove box. The intensity of illumination was checked every time before each measurement using a calibrated silicon diode with a known spectral response. J\\u2013V curves were recorded using a Kethley 2400 source-measurement unit. The active areas of all the devices were measured with the best possible accuracy just after the J\\u2013V measurements to estimate the short circuit current densities. The obtained Jsc values were reconfirmed by integrating the EQE spectra against the standard AM1.5G spectrum. The EQE spectra were obtained under normal atmospheric conditions without applying any special encapsulation or protection to the photovoltaic devices using a specially designed setup (LOMO instruments, Russia and Stanford Research Instruments, USA).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.5,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2, 99.999%), N,N-dimethylformamide (DMF), and Spiro-OMeTAD were provided by Xi\\u2019an Polymer Light Technology corp. The process of Methyl-ammonium iodide (MAI) was as same as the previous literature [25,26]. All the reagents were purchased from Alfa Aesar unless otherwise indicated.\\nThe ZnO nanoparticles were obtained according to previously reported [21]. Patterned PET/ITO (10\\u202f\\u03a9, 83%T) substrates were cleaned with ethanol, acetone, and deionized water, then dried with clean nitrogen. A compact ZnO film was deposited on the ITO surface by spin coating (3000\\u202fr, 30\\u202fs), the procedure was repeated three times. Subsequently, IL-BF4 isopropanol solution with specific concentration was quickly spin-coated (5000\\u202fr, 30\\u202fs) on the surface of ZnO ETL. A two-step solution method was used to develop MAPbI3 layer (without annealing in the second step) [27]. After the samples cooled down to room temperature, Spiro-MeOTAD was deposited at 4000\\u202frpm for 30\\u202fs. An Au electrode was thermally evaporated on the HTM layer [28].\\n\\nX-ray diffraction (XRD, Philip) confirmed the crystal structure of the film. The root-mean-squared roughness of ZnO films and the morphology of perovskite thin films were observed with atomic force microscopy (AFM, Shimadzu Company) and scanning electron microscope (SEM, FEI), respectively. XPS measurements were measured using photoelectron spectroscope (XPS, Shimadzu). UV\\u2013vis spectrophotometer (PerkinElmer) was performed to investigate the light transmittance of ZnO film and absorbance of perovskite layer. The photoluminescence (PL) spectroscopy (excitation at 532\\u202fnm) and time-resolved photoluminescence (TRPL) spectroscopy (325\\u202fnm) were collected from Ltd FLS 980 spectrometer (Edinburgh). The I-V characteristics were obtained with electrochemical workstation (CHI660C) under one-sun AM 1.5\\u202fG (100\\u202fmW\\u202fcm\\u22122) illumination. The internal impedance of devices was investigated by electrochemical impedance spectroscopy (EIS) potentiostat (IviumStat 10,800) and the frequency range from 0.1\\u202fHz to 100\\u202fMHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: PET | ITO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Single layer GR films were grown using a CVD process of the gas mixture of 30 sccm CH4 and 10 sccm H2 on a Cu foil at 1000\\u202f\\u00b0C for 5\\u202fmin under vacuum conditions. The GR/Cu stack was spin-coated with poly(methyl methacrylate) (PMMA) at 5000\\u202frpm for 1\\u202fmin and then heat-treated at 180\\u202f\\u00b0C for 1\\u202fmin. Subsequently, the Cu was then etched in Iron(III) chloride solution for 2\\u202fh. Finally, graphene was transferred onto the ITO/glass substrate. After that, the PMMA used as the supporting film was removed by using acetone. AuCl3 powder was dissolved in nitromethane to prepare AuCl3 solution from 5 to 30\\u202fmM. For doping of graphene, the solution was dropped on the whole surface of the graphene sheet, and after 1\\u202fmin elapsed, it was spin-coated at 2500\\u202frpm for 1\\u202fmin.\\n\\nTo confirm the transfer of graphene sheet on the ITO surface, micro Raman scattering was done with a 532\\u202fnm laser at \\u223c1 mW as an excitation source. Transmittance, work function, and carrier mobility were measured by using ultraviolet (UV)-visible-near IR optical spectrometer, Kelvin-probe force microscope, and Hall-effect apparatus, respectively. Topological images were obtained using a non-contact atomic force microscope (AFM) to check the uniformity of the PEDOT:PSS on ITO, GR/ ITO, and AuCl3-GR/ITO surfaces. The perovskite films deposited on each sample were analyzed by plan view scanning electron microscope images. In addition, absorption spectroscopy and X-ray diffraction (XRD) were used to check the formation of the perovskite films.\\n\\nTo fabricate the p-i-n type inverted MAPbI3 perovskite solar cells, PEDOT:PSS (Clevios, Al4083)/methanol (1:1v:v) was spin coated on an ITO, GR/ITO, and AuCl3-GR/ITO substrates at 3000\\u202frpm for 40, and then annealed at 140\\u202f\\u00b0C for 20\\u202fmin. For the perovskite layer, solution of CH3NH3PbI3 (MAPbI3) was prepared by dissolution of 1:1 ratio of methyl ammonium iodide powder (MAI, Dye sol) and lead(II) iodide powder (PbI2, Sigma-Aldrich) in N,N-dimethylformamide (DMF, Sigma-Aldrich):dimethyl sulfoxide (DMSO, Sigma-Aldrich) mixed solvent (8:2, volume ratio) at 60\\u202f\\u00b0C for 1\\u202fh. The 40\\u202fwt% MAPbI3 perovskite solution was spin-coated on the PEDOT:PSS layer by consecutive spin-coating steps at 1000 and 4000\\u202frpm for 10 and 40\\u202fs, respectively. During the second spin-coating step, toluene was quickly dropped onto the rotating substrate and subsequently dried at 100\\u202f\\u00b0C for 5\\u202fmin. After that, a phenyl-C61-butyric acid methyl ester (PCBM, nano-C)/1,2-dichlorobenzen (1,2-DCB) solution (20\\u202fmg/1 mL) was coated on the perovskite film by spin-coating at 2000\\u202frpm for 60\\u202fs. Subsequently, bathocuproine (BCP)/ethanol solution (0.5\\u202fmg/1mL) was coated on the PCBM film by spin-coating at 4000\\u202frpm for 40\\u202fs. Finally, Al electrodes were vacuum deposited through a shadow mask under 10\\u22126 Torr to fabricate a device of 0.16\\u202fmm2 area.\\n\\nThe photovoltaic parameters of the cells were measured using a solar simulator (McScinece K201) under illumination of 1 Sun (100 mWcm\\u22122 AM 1.5G). For measuring the hysteresis of the current density-voltage (J\\u2013V) curves, the forward and reverse scan rate was set to 200\\u202fms/10\\u202fmV as a standard condition. The J-V curves of all devices were measured by masking with a metal mask having an active area of 0.096\\u202fcm2. External quantum efficiency (EQE) was measured under monochromatic light generated by a Xenon arc-lamp (Oriel Apex Illuminator, Newport) in combination with a monochromator (Cornerstone 260, Newport). The spectral settings of the EQE were calibrated using commercially silicon reference cells.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: Graphene | AuCl3 | PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Lamination | Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"In a typical procedure two separated precursor solutions were prepared. One with 0.120\\u202fg of sulfur powder (S, 99.9%; Sigma Aldrich) and the other with 0.425\\u202fg of copper chloride dihydrate (Sigma Aldrich, 99.999%) dissolved in 20\\u202fml and 10\\u202fml of oleylamine (Sigma Aldrich, 70%), respectively. The latter solution was heated to reach 150\\u202f\\u00b0C and then sulfur solution was rapidly added. Reaction was maintained for 3\\u202fmin and then the mixture was cooled down to room temperature. Product was collected by centrifugation at 5000\\u202frpm for 3\\u202fmin, washed five times with ethanol to remove oleylamine remnants and finally dispersed in toluene to obtain a 47\\u202fmg/ml stable dispersion.\\n\\nChemically etched FTO glass (Nippon Sheet Glass) was sequentially cleaned by sonication in a 2% Helmanex soap solution, acetone and ethanol for 15\\u202fmin each, followed by a UV-ozone treatment for 15\\u202fmin. Then a solution of 0.045\\u202fg/ml titanium diisopropoxide bis(acetylacetonate) (Sigma-Aldrich) in anhydrous ethanol was sprayed at 450\\u202f\\u00b0C to deposit a 30\\u202fnm thick TiO2 compact layer. To form a 200\\u202fnm mesoporous TiO2 layer a 0.11\\u202fg/ml ethanol solution of a commercially available TiO2 paste (Dyesol 30NRD) was spin-coated at 2000\\u202frpm and substrates were annealed at 500\\u202f\\u00b0C for 30\\u202fmin. Afterwards, a 0.1\\u202fM solution of Li-TFSI in acetonitrile was deposited at 3000\\u202frpm for 10\\u202fs, followed by a sintering at 500\\u202f\\u00b0C for 30\\u202fmin. MAPbI3 precursor solution was prepared by mixing 1.5\\u202fM PbI2 and 1.5\\u202fM CH3NH3I in DMSO. CsFAMAPbIBr solution was prepared by mixing 1.15\\u202fM PbI2, 0.19\\u202fM PbBr2, 1.1\\u202fM formamidinium iodide (FAI) and 0.19\\u202fM methylammonium bromide (MABr) in a mixture of DMF and DMSO with a 4:1 volume ratio (solution A). Subsequently, a solution B was fabricated by mixing 1.15\\u202fM CsI and 1.15\\u202fM PbI2 in DMSO. Then solution A and B were mixed in a volume ratio of 10:1 to have the triple cation perovskite precursor. MAPbI3 was then deposited at 1000\\u202frpm for 10\\u202fs (500\\u202frpm\\u202fs\\u22121, first step) and 4000\\u202frpm for 30\\u202fs (2000\\u202frpm\\u202fs\\u22121, second step). 10\\u202fs prior to the end of the program, 100\\u202f\\u03bcl of chlorobenzene were dropped. For the CsFAMAPbIBr perovskite we used 2000\\u202frpm for 12\\u202fs (200\\u202frpm\\u202fs\\u22121), and 5000\\u202frpm for 25\\u202fs (2000\\u202frpm\\u202fs\\u22121). In this step chlorobenzene was dropped 9\\u202fs before the end of the process. Afterwards, films were annealed at 100\\u202f\\u00b0C for 60\\u202fmin. A 47\\u202fmg/ml CuS NPs dispersion was then dynamically spin-coated. Finally, the gold electrode (70\\u202fnm) was deposited by thermal evaporation.\\n\\nTransmittance of CuS NPs films were taken using PerkinElmer Lambda 1050 UV/Vis/NIR spectrophotometer. The XRD measurement was obtained with a Rigaku Ultima III X-ray diffractometer operating at 40 KV accelerating voltage and 44\\u202fmA current. For Raman spectra we used a Horiba Jobin Yvon (Labram HR) equipment with a CCD detector. Cross-section SEM-images were taken in a Hitachi-4800 UHR SEM. TEM images were obtained in a Tecnai F20 Super Twin TMP equipment. The electrical characterization of the devices was performed using a 4200SCS Keithley system at a voltage swept speed around 50\\u202fmV/s in combination with an Oriel sol3A sun simulator, which was calibrated to AM1.5G standard conditions using an Oriel 91,150\\u202fV reference cell. Conductivity measurements were performed with the four point probe employing 4200SCS Keithley. Photoelectron spectroscopy (PES) measurements were performed in a ultra-high vacuum analysis chamber (base pressure of 2\\u202f\\u00d7\\u202f10\\u221210 mbar) using a He-discharge UV source (Omicron) with an excitation energy of 21.2\\u202feV for ultraviolet photoelectron spectroscopy (UPS) and a Al K\\u03b1 X-ray source with an excitation energy of 1486.6\\u202feV for X-ray photoelectron spectroscopy (XPS). The photoelectron spectra were recorded using a Phoibos 100 (Specs) hemispherical energy analyzer at a pass energy of 5\\u202feV for the valence band, 20\\u202feV for the core level spectra, and 50\\u202feV for the survey scans. For work function determination, the secondary electron cut-off (SECO) was recorded by applying a \\u221210\\u202fV sample bias to clear the analyzer work function. A mixed Gaussian/Lorentzian peak shape and a Shirley type background were employed for XPS peak fitting with the XPS Peak 4.1 software. Samples were illuminated under white halogen lamp at a power of 150\\u202fmW\\u00b7cm-2 (daylight rendering spectrum).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: CuS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2), Spiro-OMeTAD and Methyl-ammonium iodide (MAI) were provided by Xi'an Polymer Light Technology corp. N, N-dimethylformamide (DMF) was purchased from Ying Kou You Xuan Trade Co., Ltd. Other reagents and solvents were purchased from Alfa Aesar without further purification.\\n\\nThe tin oxide (FTO)-glass substrate was cleaned by detergent twice firstly, after that, it was ultrasonically purged by acetone, ethanol, and deionized (DI) water (1:1:1). A thin layer of compact TiO2 was then deposited on the cleaned and UV-treated FTO substrate by spray pyrolysis at 500\\u202f\\u00b0C for 30\\u202fmin with a solution of titanium diisopropoxide in isopropanol. Then a mesoporous TiO2 layer was deposited on the compact TiO2 by spin-coating with a precursor solution of a diluted TiO2 paste (Dyesol 30 NR-D) in ethanol solution at 3000\\u202frpm for 30s and sintered at 500\\u202f\\u00b0C for 30\\u202fmin. The MAPbI3 perovskite films were deposited on mesoporous TiO2 by a one-step solution according to the literature []. The 0.462\\u202fg PbI2 and 0.2\\u202fg MAI were dissolved in a 1\\u202fml mixture of dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) with a ratio of 3:1 (volume ratio) as the perovskite precursor, and then the perovskite precursor was coated on the mesoporous TiO2 at 4000\\u202frpm with 30s, during which 80\\u202f\\u03bcL of chlorobenzene was dropped onto the spinning substrate at the first 7s, after that, the spin-coated mesoporous TiO2 substrates were annealed at 100\\u202f\\u00b0C for 30\\u202fmin to form the perovskite layer. SnPc was dissolved in chlorobenzene and ultrasonic overnighter. For the device with SnPc films, a thin layer was spin-coated at 3000\\u202frpm for 30\\u202fs, the spin-coating formulation was prepared by dissolving SnPc in chlorobenzene (0.2, 0.5, 1.0, 1.5\\u202fmg/ml) stirring overnight. The transport layer (HTL) of spiro-OMeTAD was deposited by spin-coating at 4000\\u202frpm for 25s. Finally, Au counter electrode was by thermal evaporation of a 100\\u202fnm thickness [,].\\n\\nX-ray diffraction (XRD) patterns were obtained to exam the crystal structure with a scan of 6\\u3002/min under the operation of Cu K\\u03b1 irradiation (\\u03bb\\u202f=\\u202f1.5406\\u202f\\u00c5). UV\\u2013vis spectra of perovskite films were measured by the Lambda 35 (Perkin Elmer) ultraviolet visible (UV\\u2013vis) spectrophotometer. The surface morphology and cross-section images of different structures were characterized by scanning electron microscope (Gemini-SEM 300), and the root-mean-square roughness (RMS) of perovskite and SnPc films were observed with atomic force microscopy (AFM, Shimadzu Company). The photoluminescence (PL) spectroscopy was measured using a Lab-RAM HR800. Water contact angle of films were obtained via the Super-hydrophobic instrument. The ultraviolet photo-electron spectroscopy (UPS) spectra were obtained by the (AXIS-ULTRA DLD-600W) X-ray photoelectron spectroscopy (XPS). The ICPE were measured by a solar cell quantum efficiency measurement system (QEXL, PV measurements, Inc.). The electrochemical impedance spectra (EIS) were used an Autolab PGSTAT 30 equipment (Eco Chemie B.V., Utrecht, The Netherlands) under dark condition. The photocurrent density-voltage (I-V) characteristics of the solar cell were obtained with electrochemical workstation (CHI660C) under one-sun AM 1.5\\u202fG (100\\u202fmW\\u202fcm\\u22122) illuminations.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: ZnPc | Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"\\nCompounds 1 (1.00\\u202fg, 2.78\\u202fmmol) and 2 (0.87\\u202fg, 3.34\\u202fmmol) were dissolved in 15\\u202fmL toluene. Then the system was conducted under reflux condition for several hours. After the solution turned white from light yellow, the reaction was cooled to room temperature. Subsequently, it was filtrated and washed by 2\\u202fmL ethanol to give white solids (compounds 3) without further purification. Then compounds 3(0.5\\u202fg, 0.805\\u202fmmol)was dissolved in 15\\u202fmL dry tetrahydrofuran. The system was stirred 20\\u202fmin\\u202fat room temperature under nitrogen atmosphere. After t-BuOK (0.18\\u202fg, 1.61\\u202fmmol) was added to the reactant system at 0\\u202f\\u00b0C, the solution turned to red color. After stirring for 10\\u202fmin, compounds 4 (0.11\\u202fmL, 0.88\\u202fmmol) was added to the mixing solution. The system was cooled to room temperature and stirred for additional 2 hours. The solvent was removed under reduced pressure, and extracted with ethyl acetate. The c crude products were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. Then it was purified with chromatography petroleum by a mixing solution (ether/ethyl acetate\\u202f=\\u202f10:1, vol%) to afford a light-yellow solid (compounds 5) with a yield of 61%. 1H NMR (400\\u202fMHz, CDCl3) \\u03b4 (ppm): 7.63 (s, 2\\u202fH), 7.21 (d, J\\u202f=\\u202f8.7\\u202fHz, 2\\u202fH), 6.83 (d, J\\u202f=\\u202f9.0\\u202fHz, 2\\u202fH), 6.58 (d, J\\u202f=\\u202f12.1\\u202fHz, 1\\u202fH), 6.32 (d, J\\u202f=\\u202f12.1\\u202fHz, 1\\u202fH), 3.86 (s, 3\\u202fH), 3.83 (s, 3\\u202fH). 13C NMR (400\\u202fMHz, CDCl3) \\u03b4 (ppm): 136.348, 132.776, 130.153, 131.697, 130.057, 127.992, 125.082, 123.017, 118.370, 117.824, 114.246, 113.844, 60.798, 55.384.\\n\\nThe synthesis route of compounds 7 is similar with that of compounds 5. The reaction affords a white solid with a yield of 82%. 1HNMR (400\\u202fMHz, CDCl3) \\u03b4 (ppm): 7.35 (s, 4\\u202fH), 6.44 (s, 2\\u202fH), 3.88 (s, 6\\u202fH). 13CNMR (400\\u202fMHz, CDCl3) \\u03b4 (ppm): 153.537, 134.651, 133.118, 132.829, 130.942, 128.858, 128.593, 118.067, 117.648, 65.588.\\n\\nCompounds 5 (0.20\\u202fg, 0.50\\u202fmmol), Pd(Ph3P)4 (0.054\\u202fg, 0.047\\u202fmmol), compounds 8 (0.62\\u202fg, 1.44\\u202fmmol), and 2.5\\u202fmL of K2CO3 solution (2\\u202fM in H2O) was dissolved in 20\\u202fmL 1,2-dimethoxyethane. The reaction system was refluxed for 10 hours under nitrogen atmosphere. The reaction was quenched by 15\\u202fmL\\u202fH2O and extracted with ethyl acetate. The crude products were washed with brine and dried over Na2SO4. The solvent was evaporated under reduced pressure and purified with chromatography petroleum with the mixing solution (ether/ethyl acetate\\u202f=\\u202f8:1, vol%) to afford a light-yellow solid (XSln847) with a yield of 75%. 1H NMR (400\\u202fMHz, CDCl3) \\u03b4 (ppm): 7.42\\u20137.38 (m, 4\\u202fH), 7.30 (s, 2\\u202fH), 7.04\\u20137.08 (m, 10\\u202fH), 6.91 (d, J\\u202f=\\u202f8.7\\u202fHz, 6\\u202fH), 6.80\\u20136.84 (m, 8\\u202fH), 6.48 (d, J\\u202f=\\u202f12.1\\u202fHz, 1\\u202fH), 6.35 (d, J\\u202f=\\u202f12.1\\u202fHz, 1\\u202fH), 3.74\\u20133.80 (m, 18\\u202fH). 13CNMR (400\\u202fMHz, CDCl3) \\u03b4 (ppm): 167.746, 159.223, 158.736, 133.485, 130.945, 130.305, 130.218, 129.883, 129.353, 128.869, 128.869, 128.253, 127.617, 126.710, 126.028, 114.703, 114.169, 113.677, 65.595, 60.470, 60.360, 55.514. HRMS (EIS) cacld for C56H50N2O6 (M+H+): 847.3669; found: 847.3637.\\n\\nThe synthesis route of XSln1453 is similar with that of XSln847. The reaction affords a brown solid with a yield of 78%. 1HNMR (400\\u202fMHz, CDCl3) \\u03b4 (ppm): 7.31 (s, 4\\u202fH), 7.25 (d, J\\u202f=\\u202f8.5\\u202fHz, 8\\u202fH),7.05 (d, J\\u202f=\\u202f8.8\\u202fHz, 16\\u202fH), 6.88 (d, J\\u202f=\\u202f8.5\\u202fHz, 8\\u202fH), 6.79 (d, J\\u202f=\\u202f8.9\\u202fHz, 16\\u202fH), 6.54 (s, 2\\u202fH), 3.76 (s, 24\\u202fH), 3.26 (s, 6\\u202fH). 13CNMR (100\\u202fMHz, CDCl3) \\u03b4 (ppm): 171.192, 167.770, 132.369, 130.982, 129.298, 128.896, 65.615, 60.443, 55.483, 54.212. HRMS (EIS) cacld for C96H84N4O10 (M+H+): 1453.6187; found: 1453.6266.\\n\\n\\nITO substrates were washed using detergent solution, deionized water, acetone, and ethanol sequentially under sonic condition. All devices were fabricated with the structure of ITO/HTM/perovskite/PCBM/BCP/Ag. The HTMs were dissolved in chlorobenzene solution with a concentration of 5\\u202fmg/mL. The HTM solution was directly deposited on the ITO substrate at 4500\\u202frpm for 40\\u202fs, followed by thermally annealing on a hotplate at 80\\u202f\\u00b0C for 30\\u202fmin. Subsequently, MAPbI3 perovskite precursor (461\\u202fmg PbI2, 159\\u202fmg MAI and 70.9\\u202f\\u03bcL DMSO dissolved in 634.92\\u202f\\u03bcL DMF) was stirred for 1\\u202fh\\u202fat 50\\u202f\\u00b0C to prepare a CH3NH3I\\u00b7PbI2\\u00b7DMSO adduct solution. The prepared perovskite precursor was spin-coated on the top of HTL at 4000\\u202frpm for 25\\u202fs, following a thermal annealing at 100\\u202f\\u00b0C for 10\\u202fmin in a nitrogen-filled glove box. After that, the PCBM solution (20\\u202fmg/ml in chlorobenzene) was spin-coated on the perovskite layer at 2000\\u202frpm for 40\\u202fs, and annealed at 80\\u202f\\u00b0C for 10\\u202fmin. A BCP solution (0.5\\u202fmg/ml in isopropanol) was deposited at 4000\\u202frpm for 40\\u202fs. Finally, a \\u223c100\\u202fnm Ag counter electrode was vapor deposited on top of the BCP layer.\\n\\nUV\\u2013vis absorption spectra were recorded on a Shimadzu UV-2600 absorption spectrophotometer. FL spectra were conducted on a Hitachi F-4500 FL Spectrophotometer. Cyclic voltammetry measurement of the HTMs were constructed in Shanghai chenghua chemical workstation by using n-Bu4NPF6 as an electrolyte with a concentration of 0.1\\u202fM/L in dichloromethane solution, platinum as a working electrode, Ag/AgCl as a reference electrode, and Pt/C as a counter electrode. 1H NMR and 13C NMR spectra were conducted using a Bruker AM-400 NMR with TMS as an interior label. The HRMS characteristics were measured with Micromass GCT-TOF. The SEM images were collected by Nova SEM 230 FE-SEM. The J\\u2013V curves were recorded with a ZHANER chemical workstation under an AM 1.5G illumination. The IPCE characteristics of the devices were measured with a self-built system of Qtest Station 2000. The EIS measurement was constructed by using a ZHANER chemical workstation. Differential scanning calorimetry (DSC) was recorded with DSC 200 F3 Maia under a nitrogen atmosphere. Surface roughness of HTMs was measured by surface scanning probe microscopy (SPM).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: XSln1453,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The ZnO (ZnO-350, Sumitomo Osaka Cement Co.) nanoparticles were used as received. The lead iodide (beads, \\u221210 mesh, 99.999% trace metals basis) and Li-TFSI (>99.0%) were purchased from Sigma-Aldrich. The CH3NH3I (>99.0%) was purchased from Xi'an Polymer Light Technology Corp. The Spiro-OMeTAD (2, 2\\u2032, 7, 7\\u2032-tetrakis-(N, N-di-4-methoxyphenylamino)-9, 9\\u2032-spirobifluorene, >99.0%) was purchased from Merck. Ultra-dry solvent of N, N-dimethylformamide (DMF, >99.9%) and isopropanol (>99.9%) were obtained from J&K and Acros, respectively. All the chemicals and solvents which were not mentioned were purchased from Sinopharm Chemical Reagent Co. Ltd and stored in N2 filled glove box and used as received.\\n\\nCovering the ZnO nanoparticles with the ZnO/ZnS was performed by adding 0.30\\u202fg of the as-grown ZnO nanoparticles to 50\\u202fmL of isopropanol and sonication for 10\\u202fmin. After adjusting the pH at 10, we added a solution of x M (x=\\u202f0.025, 0.05, and 0.1) thioacetamide (TAA) to the mixture dropwise. The solution was stirred for 2\\u202fh at 100\\u00a0\\u00b0C, and then a solution of 0.05\\u202fM ZnCl2 was added dropwise into the above mixture and stirred for 1\\u202fh. After that, the product was washed with deionized water and ethanol and dried at 70\\u00a0\\u00b0C in vacuum.\\n\\nThe pre-patterned ITO glass substrates were cleaned with detergent, deionized water, chloroform, acetone and 2-propanol in sequence. Before spin coating, the substrates were treated by plasma cleaning for 5\\u202fmin. The ZnO nanoparticles and ZnO/ZnS nanoparticles were dispersed in butanol in different blending proportion with a total concentration of 6\\u202fmg/mL and stirred for 3\\u202fh before use. The solution was filtered with a PVDF hydrophobic 0.45\\u202f\\u00b5m filter and spin-coated on ITO substrates at 3000\\u202frpm for 30\\u202fs to form a relatively compact ZnO and ZnO/ZnS thin films, and followed by short baking at 150\\u00a0\\u00b0C for 5\\u202fmin. This procedure was repeated for three times before finally baking at 200\\u00a0\\u00b0C for 1\\u202fh. The MAPbI3 and Spiro-OMeTAD films were prepared by our previously published solvent annealing method . PbI2 was dissolved in DMF at 70\\u00a0\\u00b0C. The concentration of PbI2 solution was 460\\u202fmg/mL. Then, the solution was spin-coated on the ITO at 4000\\u202frpm for 30\\u202fs. PbI2 films were kept in a petri dish for 10\\u202fmin exposure to solvent vapor in DMF vapor environment allowing a slow growth of large sized PbI2 nanoparticles as detailed in the previous investigation. This film was subsequently annealed at 70\\u00a0\\u00b0C. After cooling down, the substrates were dipped into a solution of CH3NH3I in 2-propanol (10\\u202fmg/mL) for 1\\u202fmin, and followed by rinsing with 2-propanol. The film was then dried under a flow of N2. And then this film war annealed at 70\\u00a0\\u00b0C in 20\\u202fmin. The HTL containing 80\\u202fmg Spiro-OMeTAD, 46.5\\u00a0\\u03bcL Li-TFSI and 10.5\\u00a0\\u03bcL 4\\u2011tert\\u2011butylpyridine in 1\\u202fmL chlorobenzene was spin-coated on top of the perovskite film at 4000\\u202frpm for 30\\u202fs. Finally, 100\\u202fnm of Ag was thermally evaporated on the top of HTL to form the back contact. For each condition, 10 separated devices were fabricated. The active area of PSCs as defined by a mask was 0.04\\u00a0cm2.\\n\\nThe morphologies of the films of perovskite were observed using scanning electron microscopy (SEM, Hitachi SU8020). X-ray diffraction (XRD) was measured using Rigaku SmartLab X-ray diffractometer with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.542\\u202f\\u00c5) at 25\\u00a0\\u00b0C. J\\u2013V curves of perovskite solar cell were recorded using a Keithley 2400 source meter measurement system under an AM1.5G filter at a calibrated incident intensity of 100\\u202fmW/cm. The J\\u2013V curves were measured from open-circuit to forward bias. IPCE values were measured using a commercial IPCE setup (Crowntech QTest Station 1000AD) in air under short-circuit conditions, which were equipped with a 100\\u202fW Xe arc lamp, filter wheel, and monochromator. Monochromated light was chopped at a frequency of 80\\u202fHz and photocurrents measured using a lock-in amplifier. UV\\u2013vis spectra were recorded on a Shimadzu UV-2550 spectrophotometer. The Fourier transform infrared spectrum (FTIR) was measured with Brucker VERTEX 80\\u202fV FTIR spectrometer in the range 4000\\u2212400\\u00a0cm\\u22121 at room temperature. The energy band values were remeasured with an integrated ultra high vacuum system equipped with multi-technique surface analysis system (VGScienta R3000) UPS.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 70.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 20.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Cesium Iodine (CsI) and Lead Iodine (PbI2) were bought from Xi'an Polymer Light Technology Inc (China). The poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT:PSS) aqueous solution (Clevios PVP Al4083) and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) were purchased from H. C. Starck (Leverkusen, Germany) and American Dye Sources Inc. (Baie-d'Urfe, Quebec, Canada), respectively. Lithium fluoride (LiF, 99.99%) and hydroiodic acid (HI, 45\\u202fwt%) were obtained from Sinopharm Chemical Reagent Co., Ltd. (Shanghai, China). The above materials were used as received. Indium tin oxide (ITO) coated glass substrates with a sheet resistance of 15\\u202f\\u03a9 sq\\u22121 were provided by Shenzhen Display (Shenzhen, China).\\n\\nITO-coated glass substrates were cleaned by ultrasonication in acetone, deionized (DI) water and isopropyl alcohol (IPA) for 13\\u202fmin each and then dried using high purity nitrogen gas. The substrates were then treated with oxygen plasma for 6\\u202fmin. Afterwards, 40\\u202fnm PEDOT:PSS was spin-coated (4000\\u202frpm, 20\\u202fs) on the substrates, and then baked in an oven at 160\\u202f\\u00b0C for 20\\u202fmin under air conditions. To form the CsPbI3 precursor solution, CsI and PbI2 were dissolved in DMF with 1:1\\u202fM ratio (0.5\\u202fM) and stirred for 24\\u202fh in air. 66\\u202f\\u03bcL of HI acid was added into 1\\u202fmL precursor solution before prepare perovskite films. Then, the perovskite films were prepared by spin-coating the precursor solution on the substrates at 4000\\u202frpm for 10\\u202fs. In order to improve the film quality and film thicknesses, quickly drip coating process was repeated once more. The substrates were subsequently heated at 100\\u202f\\u00b0C for 10\\u202fmin on a hot plate under air conditions (Fig. S1a). The color of the films changed from transparent light yellow to dark brown. After that, 50\\u202fnm PC61BM was spin-coated (1500\\u202frpm, 20\\u202fs) on the CsPbI3 films. The cathode consisting LiF (1\\u202fnm) and Al (100\\u202fnm) was deposited at a base pressure of 5\\u202f\\u00d7\\u202f10\\u22124\\u202fPa using a thermal evaporator. The device structure is illustrated in Fig. S1b and the active area of the devices is 0.1\\u202fcm2 defined by a shadow mask.\\nThe absorption spectra of the films on ITO glass were obtained on a scanning spectrophotometer (Varian Cary 50 UV/vis, Palo Alto, CA). Bruker D8 ADVANCE was applied to record the X-ray diffraction (XRD) patterns for perovskite films. Surface morphology of the films were characterized by Hitachi S-4800 scanning electron microscopy (SEM). The thicknesses of the films were measured by Veeco Dektak 150 surface profiler. The current density\\u2012voltage (J\\u2012V) characteristics were recorded with a Keithley 2420 source measurement unit under simulated 100\\u202fmW\\u202fcm\\u22122 (AM 1.5\\u202fG) irradiation from a Newport solar simulator. The photoluminescence spectra were obtained on a Horiba Jobin Yvon FluoroMax-4 Bench-top Spectrofluorometer.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless otherwise noted, all the reagents and chemicals were purchased from the commercial sources (Sigma Aldrich, TCI Chemicals, Alfa Aesar) and used without further purification. The flash column chromatography was performed on a column packed with silica gel (300\\u2013400 mesh). The thin layer chromatography (TLC) plates of aluminum silica gel 60 F254 (Merck) were used to monitor the reaction progress.\\n\\nThe Scheme 1 presents the synthetic pathway of TP-FTzF-TP HTM. The intermediate of thiazolo[5,4-d]thiazole-based material were synthesized by the procedures reported earlier . Compound, 5-di(furan-2-yl)thiazolo[5,4-d]thiazole (2) was synthesized by the reaction of furfural (1) and rubeanic acid. The precursor 2,5-bis(5-bromofuran-2-yl)thiazolo[5,4-d]thiazole (3) was achieved by bromination with N-bromosuccinimide. The final product was obtained by palladium catalyzed suzuki cross-coupling reactions between 3 and 4 under inert atmosphere. The details of synthesis procedure are described in the Supporting Information\\u2020 (S-1).\\n\\nThe cleaned indium tin oxide glass (ITO glass; Samsung, 10\\u201315\\u202f\\u03a9/sq, 80% transmittance in visible spectrum) substrates were treated with O2 plasma at a radio frequency (RF) power of \\u223c20\\u202fW for 30\\u202fs under an oxygen flow of \\u223c20 sccm to improve the uniformity with full surface coverage of the thin film. The O2 plasma treatment considerably enhanced the hydrophilicity of ITO layer, which improved the effective adhesion of HTM layer. Moreover, sufficient oxygenated species were introduced, and O2 plasma predominately removed the dust particles and traces of adsorbed impurities from the surface of ITO substrates. A freshly prepared solution of TP-FTzF-TP in toluene solvent was then immediately spin-coated onto O2 plasma treated ITO substrates. These substrates were then heated in an oven at 120\\u202f\\u00b0C for 15\\u202fmin. After cooling, the substrates were washed with toluene to remove any TP-FTzF-TP that was not strongly attached to the ITO electrode. Thereafter, the dissolved PbI2 solution in dimethylformamide (DMF) was spun on ITO (O2 plasma)/TP-FTzF-TP substrate at ~ 2000\\u202frpm for 30\\u202fs, transferred quickly onto a hot plate and dried at 100\\u202f\\u00b0C to vapor the residual solvent. Later, CH3NH3I solution (as prepared elsewhere ) in isopropyl alcohol (IPA) was spun at ~ 2000\\u202frpm for 30\\u202fs on top of dried PbI2 films at the room temperature and the spin coated PbI2/CH3NH3I stacking films were annealed at 100\\u202f\\u00b0C forming a thin perovskite layer. Subsequently, PC61BM (20\\u202fmg\\u202fml\\u22121 in DMF) layer and Au electrode were sequentially deposited by spin coating and thermal evaporation respectively to achieve ITO (O2 plasma)/TP-FTzF-TP/CH3NH3PbI3/PC61BM/Au.\\n\\nThe investigation of the morphology and the surface modifications were studied by the atomic force spectroscopy (AFM, Nanoscope IV, Digital Instruments, Santa Barbara, USA) and contact angle measurements (CTA480), respectively. X-ray photoelectron spectroscopy (XPS) was performed by AXISNOVA CJ109, Kratos Inc., in the range of 0\\u202f\\u2212\\u202f800\\u202feV to investigate the surface chemical compositions of ITO/TP-FTzF-TP and ITO (O2 treated)/TP-FTzF-TP thin films. Thermo-gravimetric analysis (TGA) was performed by TA instruments Q-50 thermogravimetry analyzer under inert atmosphere at a scan rate of 10\\u202f\\u00b0C/min and differential scanning calorimetry (DSC) was characterized by TA instrument DSC-2910 at a heating and cooling rate of 10\\u202f\\u00b0C/min under nitrogen atmosphere. The absorption properties were measured by using UV\\u2013Vis spectrophotometer (JASCO, V-670, Japan) and photoluminescence spectra (PL) was measured by the FP-6500 (JASCO) fluorometer in dilute chlorobenzene solvent. The Cyclic Voltammetry (CV) was analyzed using WPG 100 Potentiostat/Galvanostat (WonATech) at a scan rate of 100\\u202fmV/s with a three-electrode cell containing a glassy carbon working electrode, a saturated calomel reference electrode (SCE) and a platinum wire counter electrode. In this work, TP-FTzF-TP was dissolved in dichloromethane solvent and thin film was deposited on the glassy carbon working electrode by drop casting and dried at 60\\u202f\\u00b0C for 4\\u202fh under nitrogen. The CV measurement was performed in 0.1\\u202fM of tetra butyl ammonium hexafluoro phosphate ([nBu4N]+[PF6]-) in acetonitrile as the supporting electrolyte and measured using Fc/Fc+ as an external reference. The nuclear magnetic resonance (NMR) spectra were obtained by using JEOL FT NMR spectrophotometer in CDCl3 as reference solvent (1\\u202fH at 600\\u202fMHz and 13\\u202fC at 100\\u202fMHz. The time resolved photoluminescence was performed by iHR320, TSCPC to study the charge extraction process at ITO/TP-FTzF-TP and ITO(O2 treated)/TP-FTzF-TP interfaces. To understand the electrical properties, the current density (J)\\u2013voltage (V) measurements were performed for elucidating the performance of PSCs using computerized digital multimeter (model 2000, Keithley) with a variable load under one sun (1.5\\u202fAM at 100\\u202fmW/cm2). The simulated sunlight was supplied by using metal halide lamp of 1000\\u202fW and the light intensity was adjusted to 100\\u202fmW/cm2 (1.5\\u202fAM), using Si photo detector fitted with a Ka-5 filter as a reference (calibrated at NREL, USA). The incident photon-to-current conversion efficiency (IPCE) was carried out by a specially designed IPCE system for solar cell by IVIUM technologies. Before performing the IPCE measurements, the system was calibrated with a silicon photodiode, using the NIST-calibrated photodiode G425 as standard. The IPCE results of PSCs were collected as a function of wavelength from -300 to 1000\\u202fnm using 75\\u202fW Xe lamp as a light source for generating monochromatic beam at a low chopping frequency.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100.0 >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: TP-FTzF-TP,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The electron transporting TiO2 layer was spin coated (SETCAS Electronics Co., Ltd KW-4B) onto the FTO substrate at 5000\\u202fr.p.m. for 30\\u202fs, using precursor with 369\\u202f\\u03bcl titanium isopropoxide (Sigma-Aldrich, 99.999%) and 0.15\\u202fml 37\\u202fwt% HCl solution dissolved in 5\\u202fml ethanol (Sigma-Aldrich, 99.5%). It was annealed in air at 500\\u202f\\u00b0C for 30\\u202fmin. 5\\u202fnm-thick C60 (Sigma-Aldrich, 99.9%) and 150\\u202fnm-thick PbI2 (Sigma-Aldrich, 99%) were deposited onto the TiO2 surface using thermal evaporation under vacuum of 5\\u202f\\u00d7\\u202f10\\u22124\\u202fPa and the deposition rate of 1\\u202f\\u00c5/s was measured using quartz crystal oscillation method with sensor near the sample. The as-prepared PbI2 films were then placed face-down on a 2\\u202fcm height corundum boat with 100\\u202fmg MAI (TCI, 98%) powder uniformly dispersed at the bottom. The corundum boat was then placed into a vacuum oven preheated to 180\\u202f\\u00b0C, and then pump down to 10\\u202fkPa in no more than 10\\u202fmin (Fig. S1). The whole reaction process lasts for 30\\u202fmin for the fully formation of 3D-MAPbI3 perovskite film. To fabricate the 3D-2D perovskite structure, the as-prepared 3D-MAPbI3 perovskite film was treated by 50\\u202fmg BAI (TCI, 97%) with the procedure the same as the above, but with oven temperature set at 120\\u202f\\u00b0C for 5\\u202fmin, 10\\u202fmin, 20\\u202fmin, 40\\u202fmin and 60\\u202fmin. After the reaction, the 3D-2D perovskite film was transferred immediately into a nitrogen-filled glove box and naturally cooled down to room temperature. 25\\u202fml of 2,2\\u2032,7,7\\u2032-Tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene (Spiro-OMeTAD) solution was spin-coated onto the as-prepared perovskite film at 5000\\u202frpm for 30\\u202fs. The spiro-OMeTAD solution was synthesized according to our previous work []. The sample was then oxidized for 21\\u202fh in a cabinet with controlled humidity under 10% RH. Finally, 80\\u202fnm-thick Au was deposited onto the spiro-OMeTAD layer through thermal evaporation method under a vacuum better than 5\\u202f\\u00d7\\u202f10\\u22124\\u202fPa and a deposition rate of 0.6\\u202f\\u00c5/s.\\n\\nThe current density\\u2212voltage (J\\u2212V) characteristic was measured with a Keithley 2400 source-meter together with a sunlight simulator (Zolix Sirius-SS150A, AM 1.5G) in a glovebox. KPFM images were obtained using NT-MDT NDTGRE with tip bias. Surface potential on difference devices is calibrated using Au as reference. The XRD patterns of the prepared films were measured using Rigaku miniflex 600. Ultraviolet\\u2013visible absorption spectra were measured using SHIMADZU UV-2600. Steady-state PL spectra measurements were taken with 532\\u202fnm laser source at room temperature (Horiba, LabRAM HR Evolution Inc.). The valance band maximum (VBM) was measured using ultraviolet photoelectron emission spectroscopy (UPS) (Thermo Fisher Scientific, ESCALAB 250), using the He I (21.2\\u202feV) as excitation source.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | C60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: none >> none,\\n Perovskite_deposition_procedure: Evaporation >> Gas reaction,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"In order to fabricate the low voltage operating n-MoTe2 FET, glass substrate (Eagle 2000) was chosen. The substrate was cleaned sequentially by acetone and ethanol for 15 minutes using an ultrasonicator. We patterned gate electrode of Ti/Au (5/10\\u202fnm) on the cleaned glass substrate using conventional photolithography, DC magnetron sputter deposition and lift-off processes. A 50\\u202fnm thin Al2O3 layer was deposited by atomic layer deposition (ALD) process at 110\\u202f\\u00b0C as a gate dielectric layer. In order to prepare polystyrene-brush (PS-brush) solution, dimethyl chlorosilane terminated polystyrene (Polymer Source, Product No. P3881-SSiCl) was dissolved in toluene (Aldrich) solvent. Prior to spin-coating the PS-brush solution, the oxygen plasma cleaning (150\\u202fW, 50 sccm, 20\\u202fs) was applied to the Al2O3 surface. The PS-brush solution (10\\u202fmg\\u202fmL\\u22121) was spin-coated onto the Al2O3 surface and then heated at 170\\u202f\\u00b0C for 48\\u202fh inside a vacuum oven. During the heating, bonding reaction occurs at the interface between PS and Al2O3 surface. According to our previous work, the PS-brush produces covalent bonding between coil-like polymer chains and Al2O3 oxide layer, which is very robust to conventional organic solvent for usual photolithography process []. The surface of this 8\\u202fnm-thin PS-brush is very hydrophobic enabling hysteresis reduction due to less interface trap density between dielectric and MoTe2 channel []. Following rinsing with copious amount of toluene, remaining unreacted PS after reaction was removed, so that only ultrathin PS-brush may remain. Then the sample was again heated at 100\\u202f\\u00b0C for 24\\u202fh in a vacuum oven []. As the next step, MoTe2 nanosheet was mechanically exfoliated by polydimethylsiloxane (PDMS) and transferred onto the PS-brush treated Al2O3 substrate (See Figure S1a, b, and c where MoTe2 thickness information and its identity are characterized by atomic force microscopy scan and Raman spectroscopy, respectively). After transfer, we deposited source/drain electrode of Ti/Au (30/30\\u202fnm) by the same processes which used for the deposition of gate electrode. Finally, 30\\u202fnm thin Al2O3 was deposited for electron doping as well as top passivation of the MoTe2 nanosheet FET [].\\n\\nThe perovskite solar cells (PSCs) consist of Ag (100\\u202fnm)/bathocuproine (BCP, 8\\u202fnm)/C60 (40\\u202fnm)/MAPbI3 (450\\u202fnm)/poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA, 8\\u202fnm)/ITO. First, ITO substrate was cleaned with ultrasonication in deionized (DI) water, detergent, acetone, methanol, and DI water again. The wet-cleaned ITO substrate was exposed to UV-ozone for 15\\u202fmin\\u202fat 100\\u202f\\u00b0C and cooled at room temperature. After then, PTAA solution was prepared with the 2\\u202fmg of PTAA in the toluene (1\\u202fmL, Sigma-Aldrich) and it was spin-coated onto the ITO substrates with the 6000\\u202frpm for 40\\u202fs. The coated PTAA film was annealed for 10\\u202fmin\\u202fat 150\\u202f\\u00b0C. After then, sample was exposed to UV-ozone for 30\\u202fs\\u202fat 40\\u202f\\u00b0C. The MAPbI3 perovskite precursor solution was prepared with 159\\u202fmg of MAI (Dyesol), 461\\u202fmg of PbI2 (Alfa Aesar), and 71\\u202f\\u03bcL of dimethyl sulfoxide (DMSO, Sigma-Aldrich) were dissolved in 0.6\\u202fmL of N,N-dimethylformamide (DMF, Sigma-Aldrich). The perovskite precursor solution was spin-coated at 4000\\u202frpm for 30\\u202fs onto the PTAA film. Diethyl ether (0.5\\u202fmL, Sigma-Aldrich) was dropped onto the perovskite intermediate phase film at a delay of 8\\u202fs after the spin start []. And then the perovskite intermediate phase film was annealed at 100\\u202f\\u00b0C for 2\\u202fmin. After then, the C60 electron transport layer and BCP hole blocking layer were deposited with thermal evaporation sequentially at a deposition rate 0.1\\u202fnm\\u202fs\\u22121 and 0.05\\u202fnm\\u202fs\\u22121. Finally, a 100\\u202fnm thick Ag cathode was deposited onto the sample with deposition rates of 0.5\\u202fnm\\u202fs\\u22121. The active area of the device was 2\\u202fmm\\u202f\\u00d7\\u202f2\\u202fmm. The J-V characteristics were measured with a forward direction at a scan rate of 20\\u202fmV\\u202fs\\u22121 using a Keithley 2400 source measure unit at room temperature under the air mass 1.5G condition at 1 sun illumination with a solar simulator (McScience K401).\\n\\nDouble-sided scotch-tape (3\\u202fM) was used for bonding the MoTe2 FET and one perovskite cell placed back-to-back to form one single package device.\\n\\nAll static electrical measurements of our devices were performed with a semiconductor parameter analyzer (Agilent 4155C) in the dark at room temperature. One the one hand, all static and dynamic measurements of PV cell and integrated circuit under 465\\u202fnm (blue), 525\\u202fnm (green), 625\\u202fnm (red) and 940\\u202fnm (NIR) LED illumination were measured with the Agilent 4155C and function generator (AF310, Tektronix).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The silicon bottom cells were fabricated using square pieces (15 mm\\u00d715 mm) of a boron-doped, 1\\u20135\\u03a9, 525-\\u03bcm-thick Cz-Si wafer. For a pyramidal silicon solar cell, the silicon surface was etched using a KOH/IPA solution. After cleaning the Si substrate with acetone, IPA, and DI water, 2-\\u03bcm-thick Al was deposited on the back side of the substrate using e-beam evaporation, and a phosphorous SOD diffusant (SOD P507, Filmtronics) was spin-coated onto the front-side at 3000\\u202frpm. For the simultaneous formation of Al-BSF and an n-type emitter, the wafer was co-fired using rapid thermal annealing (RTA) at 900\\u202f\\u00b0C in an N2 atmosphere for 2\\u202fmin. Then, the phosphor-silicate glass (PSG) on the surface was removed using an HF solution for 30\\u202fs. Before depositing the passivation layer, the wafer was cleaned using RCA1 and RCA2 processes. A 70-nm SiNx-passivating layer with a refractive index of 1.97\\u202fat a wavelength of 900\\u202fnm was deposited using plasma enhanced chemical vapor deposition (PEH-600, SORONA) at 350\\u202f\\u00b0C. (For the edge isolation to make the active area exact, a 5 mm\\u00d75 mm active area was isolated using an ICP etch process.) For the top-electrode, a Ti/Ag grid pattern was formed through photolithography and a lift-off process. Finally, 1-\\u03bcm Ag was deposited using an e-beam evaporator for the back-contact electrode.\\n\\nA 70-nm-thick dense TiO2 layer was deposited on the patterned F-doped SnO2 (FTO, TEC7, Pilkingon) substrate using spray pyrolysis at 450\\u202f\\u00b0C with a titanium diisopropoxide bis(acethylacetonate) solution (Sigma-Aldrich) diluted in ethanol. A mesoporous TiO2 layer ~250-nm thick was spin-coated onto the bl-TiO2/FTO substrate using TiO2 paste (SC-HT040 paste, Sharechem) diluted in 2-methoxyethanol, and annealed at 450\\u202f\\u00b0C for 1\\u202fh on a hotplate. MAPbI3 powder (TCI Chemicals) was diluted in N\\u2013N-dimethylformamide (Sigma-Aldrich) and dimethyl sulfoxide (Sigma-Aldrich) (1:4 v/v) at various concentrations at 60\\u202f\\u00b0C and filtered using a 0.45-\\u03bcm PTFE filter. A filtered MAPbI3 solution was spin-coated onto the mp-TiO2/bl-TiO2/FTO substrate at 5000\\u202frpm for 60\\u202fs. During the spin-coating, toluene was drop-casted into the substrate within 10\\u202fs of the start of the spinning process, and the film was then dried at 100\\u202f\\u00b0C for 10\\u202fmin on a hot plate. Next, 10-mg poly(triarylamine) (PTAA, EM Index, Mw\\u202f=\\u202f17900 gmol-1) was diluted in toluene(1\\u202fml) and mixed with a 10-\\u03bcl solution of 170-mg ml\\u22121 lithium bistrifluoromethane-sulphonimidate (Sigma-Aldrich) in acetonitrile and 10 \\u03bcl of 4-tert-butylpyridine. The PTAA solution was spin-coated onto the MAPbI3/mp-TiO2/bl-TiO2/FTO substrate at 3000\\u202frpm for 30\\u202fs. For the opaque perovskite solar cell, 150\\u202fnm of Au was evaporated on top of the PTAA film as the top electrode.\\n\\nFor the semi-transparent perovskite top cell, 10-nm-thick MoO3 was deposited using e-beam evaporation with a ratio of 0.1 As\\u22121 as a buffer layer, and 150-nm thick IZO was deposited by RF-sputtering at room temperature as the transparent electrode. The RF-power of sputtering was 80\\u202fW. Moreover, 30-nm-thick IZO was deposited on the top of the silicon solar cell to make the entire active area electrically conductive. Ag-coated PMMA particles of 0.5\\u202fwt% (PMPMS-AG-1.53, Cospheric, 45\\u201353\\u03bcm size of PMMA particles are coated with 250\\u202fnm thick Ag layer.) were diluted in a transparent Norland optical adhesive (NOA83H, Norland Products) and the TCA solution was mixed using a Voltex Mixer (VW-10, DAIHAN Scientific). The TCA solution was spin-coated onto the IZO of the silicon solar cell at 3000\\u202frpm for 30\\u202fs, and the TCA-coated silicon solar cell was mechanically attached to the IZO layer of the perovskite top cell and annealed at 100\\u202f\\u00b0C for 1\\u202fh. Also, the edges of their interface were sealed with an NOA at 100\\u202f\\u00b0C for 15\\u202fmin. The active area of the final tandem devices is 0.25\\u202fcm2.\\n\\nThe theoretical reflectance and internal light energy flux of the device were computed using an optical simulation implemented using Python. For the multilayer tandem device, a generalized scattering matrix method was used. All layers were treated coherently except for c-Si. The c-Si layer was treated incoherently owing to its 525-\\u03bcm thickness, which is larger than the coherence length of sunlight. The values of the refractive index (n) and extinction coefficient (k) with the wavelength were measured using an ellipsometer (Elli-SE-UaM8, Ellipso technology Co., Korea) or extracted from the literature. The maximum current density was calculated by multiplying the simulated internal light energy flux and the photon flux with a wavelength of 350\\u20131200\\u202fnm using MATLAB.\\n\\nSquare pieces (30\\u202fmm\\u202f\\u00d7\\u202f30\\u202fmm) of a silicon substrate were cleaned using acetone, IPA, and DI water. The silicon native oxide on the silicon surface was removed by dipping into a buffered oxide etchant (BOE, HF/NH4F\\u202f=\\u202f7:1), and the Si substrate was rinsed with DI water and dried using a N2 gas flow. First, the Si substrate was immersed in a potassium hydroxide solution (45\\u202fwt% KOH) at 95\\u202f\\u00b0C for 10\\u202fmin to remove the damage to the silicon surface. After rinsing the substrate, the Si substrate was immersed into a solution mixed with KOH, IPA, and DI water (8:5:100 v/v) at 70\\u202f\\u00b0C for 40\\u202fmin to fabricate the micro-pyramidal silicon mold and rinsed with DI water and dried using a N2 gas flow. To fabricate the PDMS AR foil, the PDMS solution (Sylgard 184, Dow Corning Co.) was spin-coated onto the etched silicon mold at 3000\\u202frpm and cured at 100\\u202f\\u00b0C for 1\\u202fh. Finally, the cured PDMS foil was peeled off the silicon mold.\\n\\nThe morphology and thickness of the perovskite and TCA films were observed using scanning electron microscopy (S-4800 Cold FE-SEM, Hitachi high-Technologies). The transmittance and absorbance of the perovskite films were measured using a UV\\u2013vis spectrometer (Cary 5000, Agilent Technologies). The power conversion efficiencies of all devices were measured under simulated AM 1.5\\u202fG (100\\u202fmW/cm2) with a xenon lamp solar simulator. The J-V curves of the perovskite solar cells were measured using a black aperture mask of 0.0921\\u202fcm2 in area, and the J-V curves of the silicon solar cells and tandem solar cells were measured using a black aperture mask of 0.25\\u202fcm2 in area.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0921,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PSCs with a structure of Glass/ITO/NiOx/MAPbI3/PCBM/AgAl-Au composite NPs/LiF/AgAl were fabricated, as shown schematically in Fig. 1 .\\nThe pre-patterned indium tin oxide (ITO)/glass substrates with a sheet resistance of 10\\u202f\\u03a9/sq were cleaned by ultra-sonication sequentially in detergent, de-ionized water, acetone and isopropanol for 20\\u202fmin. After being dried in the oven, ITO coated glass substrates were treated with ultraviolet ozone for 15\\u202fmin. NiO precursor solution was then spin-coated at 4500\\u202frpm for 45\\u202fs to form a 20-nm thick film, followed by annealing at 275\\u202f\\u00b0C for 45\\u202fmin in air. In a typical synthesis, the nickel acetate tetrahydrate (Ni(CH3COO)2(4H2O) was dissolved in 2-methoxyethanol (C3H8O2) with monoethanolamine (NH2CH2CH2OH) (MEA) (Sigma-Aldrich) (0.1\\u202fmol/L). The mole ratio of Ni2+: MEA was maintained at 1:1 in solution. Then the solution was stirred in a glass vial under air at 70\\u202f\\u00b0C for 4\\u202fh. The solution appeared homogeneous and deep green after approximately 40\\u202fmin []. After stirring, the solution was stored in a refrigerator at 5\\u202f\\u00b0C. Then NiOx films were allowed to cool down before being transferred to a nitrogen-filled glovebox for further processing. The perovskite precursor solution was prepared by dissolving 1\\u202fM methyl ammonium iodide (MAI, 1-Material Inc.) and 1\\u202fM lead (\\u2161) iodide (PbI2, 99.9%, Aladdin Reagents) in a mixture of dimethyl sulphoxide (DMSO, AR 99% GC, Aladdin Reagents) and \\u03b3- Butyrolactone (GBL, AR 99% GC, Aladdin Reagents) (7:3 v/v). After stirring overnight, the solution was ready for use. The CH3NH3PbI3 (MAPbI3) film was spin-coated on the surface of NiOx hole-transport layer by a consecutive two-step spin-coating process at 1500\\u202frpm for 15\\u202fs and 4000\\u202frpm for 60\\u202fs, respectively. During the second spin-coating step at 30\\u202fs, 0.5\\u202fml of anhydrous chlorobenzene (Alfa Aesar) was quickly dropped onto the surface of perovskite layer, then the substrate was heated at 100\\u202f\\u00b0C for 10\\u202fmin. After being cooled down, the [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) solution (10\\u202fmg/ml in chlorobenzene) was spin-coated at 1200\\u202frpm to form a 40-nm thick film on top of the perovskite layer. Finally, A 3-nm thick AgAl, different nominal thicknesses of Au and LiF spacer, and 100-nm thick AgAl electrode were sequentially deposited by thermal evaporation with a base pressure of 3\\u202f\\u00d7\\u202f10\\u22124\\u202fPa using a shadow mask of 0.1\\u202fcm2. The weight ratio (wt%) of Al to Ag in the AgAl alloy, purchased from Trillion Metals Co., Ltd. (Beijing, China), is 3\\u202fwt%. A mask with an aperture area of 0.09\\u202fcm2 was used for the current density-voltage (J-V) characteristic measurement to avoid the edge effect.\\nThe J-V characteristics of PSCs were measured with a Keithley 2440 SourceMeter together with a Newport solar simulator with an AM1.5G illumination of 100\\u202fmW/cm2 calibrated with a standard silicon reference cell. The incident-photon-to-current conversion efficiencies (IPCEs) of the PSCs were measured over the wavelength range from 300 to 800\\u202fnm using a Newport Optical Power Meter 2936-R controlled by TracQ Basic software, where the baseline were calibrated with a detector (model 71683 v3, Oriel Instruments). The electrochemical impedance spectra (EIS) were measured in the dark using an electrochemical workstation (Autolab PGSTAT302\\u202fN). The absorption and reflectivity spectra of samples were measured using a UV/vis spectrophotometer (Hitachi U-3900). The surface morphologies of samples were investigated by field-emission scanning electron microscopy (FESEM, Hitachi S-4800). Ultraviolet photoelectron spectroscopy (UPS) spectra were measured with a monochromatic He I light source (21.22\\u202feV) and a VG Scienta R4000 analyzer.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: AgAl,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methyl 4-hydroxybenzoate, butyl 4-hydroxybenzoate, 4-Nitrophthalonitrile, Cu(OAc)2\\u00b7H2O, Zn(OAc)2\\u00b72H2O, 1,5-diazabicyclo [4.3.0] non-5-ene (DBU) were purchased from Aladdin. All of the solvents were analytically pure quality and obtained from commercial suppliers. 30NRT TiO2 paste, MABr and FAI were purchased from Greatcell Solar. PbI2 and PbBr2 were from TCI Corporation. Spiro-OMeTAD were received from Advanced Election Technology Co.,Ltd. Substrates are patterned fluorine-doped tin oxide coated glass (<15/square) obtained from Advanced Election Technology Co.,Ltd.\\n\\nInfrared and 1H NMR spectra were recorded on BIO-RADFIS3000 spectrophotometer in KBr pellets and Varian 300\\u202fMHz spectrometer in CDCl3 respectively. Mass spectra were recorded on a Matrix Assisted Laser Desorption Ionization (MALDI) Bruker Autoflex TOF (III) (matrix: 2,5-dihydroxybenzoicacid (DHB)). UV\\u2013visible/NIR and Fluorescence spectra in DMF were recorded on a Nicoet Evolution 300 spectrophotometer and a FluoroLog3 (HORIBA Jobin Yvon) steady-state system at room temperature. Thermo gravimetric analyses were recorded on a Q500 Thermo gravimetric analyzer under a flowing N2 stream []. SEM (XL30S-FEG, FEI, USA) imaging was performed with an electron beam voltage of 3\\u202fkV and current of 3\\u202fnA in the immersion-lense mode. Photoluminescence (PL) spectra were recorded with Fluorolog-Horiba fluorometer. Illumination of the solar cells was set at 100\\u202fmW\\u202fcm\\u22122 (AM 1.5G) made with an Oriel solar simulator 91160A, the current density-voltage (J-V) characteristics were recorded with Keithley 2602 Source Meter, a mask of window of 0.16\\u202fcm2 was applied to confirm the effective area of the solar cells. The setting time was 0.01\\u202fs and the delay time was 0\\u202fs. The incident photon-to-electron conversion efficiency (IPCE) was obtained with a lab-made IPCE testing system. Hole mobility of HTMs was investigated by the space-charge-limited current (SCLC) method, whose structure of hole-only device are ITO/PEDOT:PSS (40\\u202fnm)/HTM (80\\u202fnm)/MoO3 (10\\u202fnm)/Al (100\\u202fnm). The charge mobility (\\u03bc) is calculated by following equation: []. J=98\\u03bc\\u03b5o\\u03b5rv2L3\\nHere, the L is distance between two electrodes, \\u03b5 o is the free-space permittivity, \\u03b5 r is the dielectric constant of the active layer.\\n\\nAt room temperature, 5.9\\u202fmmol 4-nitrophthalonitrile (1.021\\u202fg) was dissolved in redistilled dimethylformamide (DMF, 40\\u202fmL) and then 8.26\\u202fmmol aryl phenol (methyl 4-hydroxybenzoate 1.256\\u202fg or butyl 4-hydroxybenzoate 1.602g) was added. After 15\\u202fmin stirring, finely ground K2CO3 (1.140\\u202fg, 8.26\\u202fmmol) was added for three times. The reaction was not ended until all 4-nitrophthalonitrile disappeared by thin layer chromatography (TLC) monitoring. The yellowish precipitate was obtained by pouring the mixture into cold water (100\\u202fmL). It was dealed with 1% NaOH till pH to 9\\u201310 and precipitated for a night.\\nThe filtered crude product (4-(4-methyl formate) phenoxy phthalonitrile) was recrystallized in DMF and ethanol to give milky white crystals. Yield: 1.60\\u202fg, 97.4%, m.p. 148\\u2013150\\u202f\\u00b0C. IR \\u03bd max/cm\\u22121 (KBr pellet): 3081 (CHar), 2236 (C\\u2261N), 1719 (C=O), 1594, 1486 (C=C), 1251 (Ph-O-Ar) (Fig. S1); (4-(4-butyl formate) phenoxy phthalonitrile) was recrystallized in ethanol to give yellowish crystals. Yield: 1.82\\u202fg, 96.2%, m.p. 124\\u2013126\\u202f\\u00b0C. IR \\u03bd max/cm\\u22121 (KBr pellet): 3069 (CHar), 2228 (C\\u2261N), 1718 (C=O), 1592, 1481 (C=C), 1245 (Ph-O-Ar) (Fig. S2).\\n\\nCuPcNO2-OMFPh was synthesized as follows: 4-(4-methyl formate) phenoxy phthalonitrile 1.390\\u202fg (5.0\\u202fmmol), 4-nitrophthalonitrile 0.294\\u202fg (1.7\\u202fmmol) and Cu(OAc)2\\u00b7H2O 0.339\\u202fg (1.7\\u202fmmol) were added to a 100\\u202fmL four-necked flask, 40\\u202fmL octanol and 10 drops DBU were put into the flask at the same time. The mixture was refluxed with a magnetic stirrer for 30\\u202fh under nitrogen atmosphere. The reaction mixture became to navy blue and all of the phthalonitriles were disappeared by TLC detection. The solid was purified by ethyl acetate, ethanol and water extracting respectively till the solvent becoming to colorless. The blackish green crude product was purified by silica gel column chromatography using dichloromethane and ethanol as eluent (30:1). Yield: 0.679\\u202fg, 36.8%; IR \\u03bd max/cm\\u22121 (KBr pellet): 2923 (CHar), 1718 (C=O), 1598\\uff5e1300 (C=C, Ph), 1236 (Ph-O-Pc), 1000-700 (C=C Pc) (Fig. S3); 1H NMR (CDCl3) \\u03b4ppm: 3.85 (m, 9H, CH3), 6.27 (m, 6H, Ph-H), 6.39 (m, 3H, Pc-H), 7.01 (m, 1H, Pc-H), 7.10 (d, 3H, Pc-H), 7.19 (d, 6H, Ph-H), 7.25 (d, 3H, Pc-H), 7.75 (d, 1H, Pc-H), 8.10(d, 1H, Pc-H); MS (MALDI-TOF) m/z: Calc. m/z: Calc. 1070, Found: 1070.\\n\\nCuPcNO2-OBFPh was synthesized and purified as CuPcNO2-OMFPh with the materials of 4-(4-methyl formate) phenoxy phthalonitrile 1.600\\u202fg (5.0\\u202fmmol), 4-nitrophthalonitrile 4-nitrophthalonitrile 0.294\\u202fg (1.7\\u202fmmol) and Cu(OAc)2\\u00b7H2O 0.339\\u202fg (1.7\\u202fmmol). Yield: 0.834\\u202fg, 40.5%; IR \\u03bd max/cm\\u22121 (KBr pellet): 2925 (CHar), 1717 (C=O), 1603\\uff5e1300 (C=C, Ph), 1229 (Ph-O-Pc), 1000-700 (C=C Pc) (Fig. S4); 1H NMR (CDCl3) \\u03b4ppm: 0.88 (m, 9H, CH3), 1.26 (m, 6H, CH2), 1.90 (m, 6H, CH2), 3.65 (m, 6H, CH2), 6.29 (m, 6H, Ph-H), 6.36 (m, 3H, Pc-H), 6.85 (m, 1H, Pc-H), 7.06 (d, 3H, Pc-H), 7.15 (d, 6H, Ph-H), 7.20 (d, 3H, Pc-H), 7.70 (d, 1H, Pc-H), 8.06 (d, 1H, Pc-H); MS (MALDI-TOF) m/z: Calc. m/z: Calc. 1196, Found: 1196.\\n\\nZnPcNO2-OBFPh was synthesized and purified as CuPcNO2-OMFPh with the materials of 4-(4-butyl formate) phenoxy phthalonitrile 1.600\\u202fg (5.0\\u202fmmol), 4-nitrophthalonitrile 0.294\\u202fg (1.7\\u202fmmol) and Zn(OAc)2\\u00b72H2O 0.373\\u202fg (1.7\\u202fmmol). Yield: 0.612\\u202fg, 29.7%; IR \\u03bd max/cm\\u22121 (KBr pellet): 2921 (CHar), 1713 (C=O), 1605\\uff5e1300 (C=C, Ph), 1222 (Ph-O-Pc), 1000-700 (C=C Pc) (Fig. S5); 1H NMR (CDCl3) \\u03b4ppm: 0.88 (m, 9H, CH3), 1.27 (m, 6H, CH2), 1.90 (m, 6H, CH2), 3.76 (m, 6H, CH2), 6.24 (m, 6H, Ph-H), 6.36 (m, 3H, Pc-H), 6.98 (m, 1H, Pc-H), 7.08 (d, 3H, Pc-H), 7.17 (d, 6H, Ph-H), 7.22 (d, 3H, Pc-H), 7.72 (d, 1H, Pc-H), 8.08 (d, 1H, Pc-H); MS (MALDI-TOF) m/z: Calc. m/z: Calc. 1197, Found: 1197.\\n\\n\\nA 30\\u202fnm-thickness compact TiO2 layer, 200\\u2013300\\u202fnm mesoporous TiO2 layers and perovskite layer ([(FAI)0.85(PbI2)0.85(MABr)0.15(PbBr2)0.15]) were prepared according to the reported methods []. The HTMs layers were spin-coated on the top of TiO2/perovskite films at 3000\\u202frpm for 20\\u202fs with a concentration of 20\\u202fmgmL\\u22121. For comparison, perovskite solar cells based on Spiro-OMeTAD were also fabricated by using a chlorobenzene solution doped with Lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) and 4-tert-butylpyridine (tBP) under the same conditions. All the above fabrication processes were carried out in air. Finally, 80\\u202fnm-thickness Au photocathode was deposited by thermal evaporation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: ZnPcNO2-OBFPh,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Tetraethoxysilane (TEOS) was procured from Sigma Aldrich. TEOS was used as a precursor for SiO2 nanosphere ARC coatings. Ethanol also obtained from Sigma Aldrich was used as the solvent NH3\\u20223H2O was purchased from Aladdin Industrial Corporation and used for the catalysis of the sol.\\nA hybrid silica sol was prepared by mixing the precursor materials (Jun et al., 2008). Initially, 1.5\\u202fmL of NH3\\u00b73H2O solution (10\\u202fwt%) was mixed with deionized (DI) water (6 mL), ethanol (70\\u202fmL) in a 100\\u202fmL flask by magnetic stirring. Then, 3\\u202fmL of TEOS was added drop by drop to the mixture. The final mixture was magnetically stirred for 30\\u202fmin. The silica sol obtained was kept at room temperature (RT) for at least 1\\u202fday for aging and finally used for deposition on external-facing surfaces of TCO transparent substrates of PSCs.\\n\\nFTO slides (Pilkington TEC 15) were patterned by etching with Zn powders and 2\\u202fM HCl. The etched slides were then cleaned with liquid detergent, acetone, ethyl alcohol and DI water for 15\\u202fmin, sequentially, to remove the organic or inorganic residues, and finally dried in a vacuum oven. Titanium isopropoxide (TTIP) (200\\u202f\\u03bcL) and ethanol (5\\u202fmL) were mixed to prepare a clear precursor sol. The precursor sol was spin-coated onto the etched FTO substrate at 4500\\u202frpm, followed by annealing at 500\\u202f\\u00b0C to form a compact TiO2 (c-TiO2) layer. Diluted TiO2 pastes were prepared by mixing TiO2 paste (Dyesol 18NR-T, 0.1\\u202fg) and anhydrous ethanol (444\\u202f\\u03bcL). The mesoporous TiO2 (p-TiO2) layer was deposited on the c-TiO2 layer by spin-coating the diluted TiO2 pastes at 2000\\u202frpm for 30\\u202fs. The layers were then sintered at 500\\u202f\\u00b0C for 30\\u202fmin in air. After cooling down to the RT, the samples were treated using the TiCl4 aqueous solution at 70\\u202f\\u00b0C for 30\\u202fmin and dried at 500\\u202f\\u00b0C for 30\\u202fmin. The perovskite MAPbI3 absorber was grown via a spin-coating process using a GBL/DMSO solution of PbI2 and MAI. Briefly, a pure perovskite-precursor solution (1.25\\u202fmol\\u202fL\\u22121) was prepared by mixing MAI (0.1975\\u202fg) powders and lead iodide PbI2 (0.5785\\u202fg) in GBL (700\\u202f\\u03bcL) and DMSO (300\\u202f\\u03bcL) at 60\\u202f\\u00b0C for 12\\u202fh. The formed precursor solution was deposited onto the p-TiO2/c-TiO2/FTO sample via a successive two-step spin-coating process, at 2000\\u202frpm for 30\\u202fs and at 3500\\u202frpm for 50\\u202fs, respectively. Anhydrous diethyl ether was dripped onto the center of the sample in the second spin-stage during the spin-coating process (Luo et al., 2017). The perovskite-precursor coated sample was heated and dried on a hot plate at 110\\u202f\\u00b0C for 30\\u202fmin. The hole-transport material (HTM) was deposited on the grown perovskite absorber by spin-coating a spiro-OMeTAD solution at 4000\\u202frpm for 30\\u202fs. 100\\u202fnm thick AgAl alloy film with an active area of 0.1\\u202fcm2 was formed via evaporation on the Spiro-OMeTAD-coated film (Jiang et al., 2016). Finally, SiO2 nanosphere based ARCs were deposited on the front glass surface of the as-prepared PSC solar cell by spin-coating of the aged silica sol with various spin-coating speeds from 400 to 4000\\u202frpm.\\n\\nThe morphologies of SiO2 nanosphere based ARC films were characterized by a high-resolution field emission scanning electron microscope (FESEM, Hitachi S4800). Optical spectra of SiO2 ARCs were examined and characterized by means of ultraviolet\\u2013visible light (UV\\u2013vis) spectrometer (Hitachi, U-3010). Photocurrent density\\u2013voltage (J-V) measurements were performed using an AM 1.5 solar simulator equipped with a 1000\\u202fW Xenon lamp (Model No. 91192, Oriel, USA). The solar simulator was calibrated by using a standard silicon cell (Newport, USA). The light intensity was 100\\u202fmW\\u202fcm\\u22122 on the surface of the test cell. During device photovoltaic performance characterization, a metal aperture mask with an opening of about 0.09\\u202fcm2 was used. External quantum efficiency (EQE) measurements (74125, Oriel, USA) were also carried out for these solar cells.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 110,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: AgAl,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All anhydrous solvents, including isopropanol alcohol (IPA), N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), chlorobenzene (CB), dichlorobenzene (DCB) were purchased from Sigma Aldrich. Nickel nitrate hexahydrate (99.999%) and bathocuproine (BCP) were also purchased from Sigma Aldrich. PC60BM (99.5%) was purchased from Solenne BV. Formamidinium iodine (FAI) and methylammonium bromide (MABr) were purchased from Dyesol. PbI2 and PbBr2 were purchased from Tokyo Chemical Industry Co., Ltd.\\nAgNWs with average diameter/length (D/L) of 40\\u00a0nm/45\\u00a0\\u00b5m in IPA were purchased from ACS Material (SKU: NWAG04I1). AgNWs with average D / L\\u00a0=\\u00a080\\u00a0nm/81\\u00a0\\u00b5m were synthesized. Patterned indium tin oxide (ITO) glass substrates (10\\u00a0\\u03a9/\\u25a1) were purchased from Xinyan Technology Ltd.\\n\\nThe preparation of NiOx nanoparticle ink is similar to a previously reported procedure (H. Zhang et al., 2016). Ni(NO3)2 (3.635\\u00a0g) was dissolved in 2.5\\u00a0ml of water. Ni(OH)2 was then precipitated with\\u00a0~\\u00a02.5\\u00a0ml of 10\\u00a0M NaOH solution. The light green precipitation was collected by centrifugation and washed thrice with deionized (DI) water. Afterwards, it was transferred to an oven at 80\\u00a0\\u00b0C and dried until the colour turned dark green. This solid was then transferred to an oven at 270\\u00a0\\u00b0C and kept for 2\\u00a0h. The final product was a black powder of NiOx nanoparticles. The NiOx nanoparticles were then dispersed in DI water at 2.6\\u00a0wt%. After sonicating for 2\\u00a0h, the ink was filtered through a 0.45\\u00a0\\u00b5m PVDF filter. For best results, the ink was used at least one day after filtration.\\n\\nAs-received AgNW dispersion was first purified by gentle centrifugation at 2000\\u00a0rpm for 30\\u00a0min. The AgNW precipitate was then redispersed in anhydrous IPA. Before using the AgNW dispersion, a sonication of not more than 30\\u00a0s was performed.\\n\\nThe PCBM solution was prepared by dissolving PC60BM in DCB (23\\u00a0mg/ml). The PCBM solution was then filtered through a 0.45\\u00a0\\u00b5m PTFE filter. The 10\\u00a0mg/ml C60 solution in DCB was similarly prepared. To facilitate the dissolution, the solutions were heated at 60\\u00a0\\u00b0C for 2\\u00a0h.\\nPerovskite precursor solution was prepared by dissolving 264.5\\u00a0mg of PbI2, 94.0\\u00a0mg of FAI, 37.2\\u00a0mg of PbBr2 and 11.3\\u00a0mg of MABr in 400\\u00a0\\u00b5l of DMF and 100\\u00a0\\u00b5l of DMSO (Ye et al., 2018). The solution was heated up to 60\\u00a0\\u00b0C before deposition.\\n\\nThe schematic structure of the fabricated planar perovskite solar cells is shown in Fig. 1 . The NiOx (HTL), perovskite, PC60BM (ETL) layers were sequentially spin-coated on cleaned ITO/glass substrates. ITO glass substrates were cleaned by sonication in detergent (2% Hellmanex\\u00ae III solution), DI water, acetone and IPA. After drying, the substrates were UV ozone treated for 10\\u00a0min at 100\\u00a0\\u00b0C right before deposition. NiOx ink was spin-coated on the ITO substrates at 3000\\u00a0rpm for 45\\u00a0s; the substrates were then dried on a hot plate at 100\\u00a0\\u00b0C for 10\\u00a0min. Then, perovskite film of FA0.81MA0.15Pb(I0.836Br0.15)3 was deposited by spin-coating the perovskite precursor solution with anti-solvent technique in a glovebox (Ye et al., 2018). The spin coating was done at 2000\\u00a0rpm for 10\\u00a0s and then at 6000\\u00a0rpm for 30\\u00a0s. CB (100\\u00a0\\u00b5l) was dropped on the substrate ~10\\u00a0s into the second stage of spin-coating. Upon finishing, the substrate was promptly transferred on a hot plate at 100\\u00a0\\u00b0C and kept for 50\\u00a0min. The PCBM solution (23\\u00a0mg/ml in DCB) was spin-coated at 1300\\u00a0rpm for 40\\u00a0s to form an ETL on top of the perovskite layer. The substrate was again annealed at 100\\u00a0\\u00b0C for 5\\u00a0min and cooled down before the electrode deposition.\\n\\nSpin-coating of AgNW electrodes\\nOn the PCBM layer, a AgNW top electrode was deposited by spin-coating the AgNW dispersion (10\\u00a0mg/ml) at 900\\u00a0rpm for 30\\u00a0s and dried at 90\\u00a0\\u00b0C for 30\\u00a0s. The patterned area of the AgNW electrode was delimited by polyimide tape as mask. The active cell area was defined by the overlap of the patterned ITO and the patterned AgNW electrode, typically 0.09\\u00a0cm2 for each cell.\\nThe electrode thickness can be increased by repeating the spin-coating process. Devices with 1, 2 and 3-layered AgNW electrodes were fabricated.\\nTo deposit the PCBM or C60 filler, a 10\\u00a0mg/ml solution of the respective filler was spin-coated on the AgNW layers at 1300\\u00a0rpm for 45\\u00a0s.\\nThermal evaporation of silver film electrodes\\nFor comparison, control devices with thermally evaporated Ag top electrode were also fabricated. BCP (0.5\\u00a0mg/ml solution in anhydrous IPA) was first spin-coated on the PCBM ETL at 5000\\u00a0rpm for 30\\u00a0s. The devices were then masked, and silver was deposited under a vacuum condition of 5\\u00a0\\u00d7\\u00a010\\u22126 mbar at about 0.1 \\u00c5/s.\\n\\nThe surface morphologies of the AgNW films were investigated using a microscope (Olympus BX51), and a SEM (JEOL JSM-7001F) at 10\\u00a0kV. Film transmittance spectra were recorded using a UV\\u2013visible-near IR scanning spectrophotometer (UV-3600, Shimadzu). Film thicknesses were measured using a surface profiler (KLA-TENCOR P-10). The work function of the electrode was measured using a photoelectron spectrometer (Riken Keiki, AC-2). The photoluminescence (PL) measurements were conducted using Shimadzu UV-2501 spectrofluorophotometer with an excitation wavelength of 520\\u00a0nm.\\nCurrent density-Voltage (J-V) characteristics for solar cell devices were measured in a nitrogen atmosphere with a solar simulator (SAN-EI Electric XES-301S 300\\u00a0W Xe lamp JIS Class AAA) which was calibrated to 1000\\u00a0W/m2 with a reference Si cell. For the stability test, the devices were stored in a nitrogen glovebox (H2O\\u00a0<\\u00a05\\u00a0ppm, O2\\u00a0<\\u00a010\\u00a0ppm).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.81MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-np,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag-nw | C60,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Spin-coating | Spin-coating,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The ITO/PEDOT:PSS/CsPbBr3 samples for the nanoscale characterization were prepared as follows. ITO glass substrate (Lumtec, 18 \\u03a9/sq.) was sequentially cleaned with acetone and isopropanol in an ultrasonic bath for 10 min followed by oxygen plasma cleaning for 15 min. Poly(2,3-dihydrothieno-1,4-dioxin)-poly(styrenesulfonate) (PEDOT:PSS) (Clevios PH) was spin-coated (3000 rpm) on the clean ITO substrates, followed by thermal annealing at 180 \\u00b0C for 10 min inside the glove box. The perovskite CsPbBr3 layer was deposited by thermal co-evaporation of CsBr (99.9% from Sigma Aldrich) and PbBr2 (99.9% from Sigma Aldrich) in a vacuum chamber integrated inside MBraun glove box (5\\u00b710\\u22126 Torr) at the rate of 5 \\u00c5/s to achieve the total film thickness of 300 nm. The prepared CsPbBr3 films were annealed at 130 \\u00b0C for 15 min inside the glove box and then stored in dark either at room temperature (reference non-aged samples) or at 45 \\u00b0C (thermally aged samples) during 300 h.\\n\\nThe planar junction solar cells were fabricated by spin-coating the [6,6]-Phenyl C61 butyric acid methyl ester ([60] PCBM) solution (30 mg/mL in chlorobenzene) on the top of the thermally aged and non-aged CsPbBr3 samples (prepared as described above) at 1500 rpm for 60 s under inert atmosphere inside the glow box. Silver electrodes (100 nm) were thermally evaporated through a shadow mask on the top of the perovskite films under high vacuum (4\\u20136\\u00b710\\u22126 Torr). The device area was ~0.45 \\u0441m2 as defined by the shadow mask.\\n\\nAll scanning probe microscopy measurements were conducted on Cypher ES microscope (Asylum Research, CA) under dry inert Ar atmosphere in a MBraun glovebox with O2 < 0.1 ppm and H2O < 1 ppm. Electrical contact to the sample was provided through ITO and conductive Ag paint.\\nSurface potential (V CPD) was measured by 2-pass Kelvin Probe Force Microscopy (KPFM) method in the amplitude modulation mode . Pt coated cantilever with 143 kHz resonance frequency and 4.5 N/m spring constant was used. During the second pass the cantilever was lifted by a height of 20 nm. Sample was always grounded. The cantilever was calibrated on a freshly cleaved highly oriented pyrolytic graphite (HOPG) with work function 4.6 eV . Work function of CsPbBr3 was calculated using equation VCPD=Wtip\\u2212Wsample\\u2212e. Note that while this equation is only valid for the case of metallic sample surface and metal coated cantilever under vacuum conditions, it is also sufficiently used for semiconductors if space-charge layer is considered .\\nPhotocurrent was measured in a conductive SPM mode (c-SPM) under the short circuit condition and with 500 mV bias applied to the sample. A fully platinum cantilever from Rocky Mountain (25PT300B) was used. As the light source we used the Cypher Blue Drive laser diode with 405 nm wavelength. Power density was set to 122 mW/cm2. The light was guided through the optical system of the SPM microscope from the top ( Fig. 1). The Rocky Mountain cantilever's tip projects in front of the lever, thus the tip-sample contact point is not shaded by the lever during illumination. Fully platinum tip body ensure stable and uniform contact over full scanning time.\\n\\nThe current-voltage (J-V) characteristics of the devices were obtained under the simulated 100 mW/cm2 AM1.5 solar irradiation provided by the KHS Steuernagel solar simulator integrated with an MBraun glove box. J-V curves were recorded under an inert atmosphere using Kethley 2400 source-measurement unit. The EQE spectra were measured under normal atmospheric conditions without applying any special encapsulation or protection to the photovoltaic devices using a specially designed setup composed of optical chopper SR540 (Stanford Research Systems, USA), 75 W xenon lamp, monochromator and turret with automatically shifting optical filters (LOMO instruments, Russia).\\nThe optical spectra were measured for the CsPbBr3 perovskite films deposited on the glass substrates using AvaSpec-2048-2 UV\\u2013vis spectrophotometer installed inside an argon glove box (presented in Supplementary Fig. 1 (a)).\\nThe X-ray diffraction (XRD) patterns were measured for the CsPbBr3 perovskite films deposited on the glass substrates using Bruker D8 ADVANCE diffractometer (presented in Supplementary Fig. 1 (b)).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBr3,\\n Perovskite_composition_short_form: CsPbBr,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: none,\\n Perovskite_deposition_procedure: Co-evaporation,\\n Perovskite_deposition_thermal_annealing_temperature: 130,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.4,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All reagents and solvents were used as received without any further purification. Polycrystalline FA4GeIISbIIICl12 was precipitated by mixing of 0.886\\u202fg Formamidinium chloride (HC(NH2)2Cl, 0.5\\u202fmmol) to a solution of Sb2O3 (0.342\\u202fg, 2.5\\u202fmmol) and 0.216\\u202fg Germanium dichloride (GeCl2, 1.5\\u202fmmol) in 5.0\\u202fmL of HCl (2\\u202fM). The resultants were filtered on a glass frit and dried under reduced pressure to afford 1.308\\u202fg (90.6% yields) of product. The final products for structure study were obtained by heating a solution of FA4GeIISbIIICl12 in concentrated HCl to 110\\u202f\\u00b0C in a pressure vessel. The solution was then slowly cool down to room temperature (RT) over the course of one day. Single crystalline can be also obtained by slowly cooling down a solution of FA4GeIISbIIICl12 in concentrated HCl and the structure were confirmed by using single crystal X-ray diffraction (SCXRD) studies.\\nF-doped SnO2-coated glass substrate was etched with Zn powder and HCl (2\\u202fM) for obtaining electrode pattern. Under sonication, the substrate was washed sequentially by diluted detergent, deionized water and ethanol, respectively, and then dried by nitrogen gas. Next, the substrate was treated by ozone plasma for half hour. Titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol) diluted in ethanol (1: 9 in v/v) was sprayed on the substrate and heated at ~ 500\\u202f\\u00b0C for half hour to form a blocking layer of TiO2 (70\\u201380\\u202fnm). Then, after cooling to RT, the substrate was treated in 40\\u202fmM TiCl4 for half hour at 80\\u202f\\u00b0C, followed by annealing at 500\\u202f\\u00b0C for half hour. TiO2 paste diluted in ethanol (3: 8 w/w) was spin-coated onto the blocking layer to form a mesoporous TiO2 layer. The substrate was treated in 20\\u202fmM TiCl4 solution at 80\\u202f\\u00b0C for half hour and annealed at 500\\u202f\\u00b0C for half hour before deposition of FA4GeIISbIIICl12 perovskite.\\nSolution was prepared by dissolving solid-state powder FA4GeIISbIIICl12 perovskite (1\\u202fM) in dimethylformamide (DMF) and filtered using 0.2\\u202f\\u00b5m filter. The filtered solution was deposition on the TiO2 substrates by spin-coating at 5000\\u202frpm for 30\\u202fs, with annealing at 80\\u202f\\u00b0C for 15\\u202fmin. Au electrodes were deposited on these substrates by thermal evaporation. Spiro-OMeTAD was dissolved in chlorobenzene (75\\u202fmg/mL) and spin-coated on the substrates, forming hole transporting layer.\\n\\nPhase characterization was done by Powder X-ray diffraction (XRD) measurements on a Bruker AXS (D8 Advance) X-ray diffractometer with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.54\\u202f\\u00c5) with a step size of 0.02\\u00b0 and a time per step of 1\\u202fs. Morphologies were characterized using field-emission scanning electron microscope (JEOL JSM-7600F) with an accelerating voltage of 5\\u202fkV. Thermogravimetric (TG) and differential scanning calorimetry (DSC) analysis were performed on a SDT-Q600 (TA Instruments) over a temperature range from RT to 800\\u202f\\u00b0C in nitrogen with a platinum pan at a heating rate of 5\\u202f\\u00b0C/min. The absorbance spectra were recorded using a microspectrometer (SD1200-LS-HA, Allied Scientific Pro (ASP), Quebec, Canada) with spectral resolution of 1.3\\u20135.0\\u202fnm FWHM, and the detection wavelength range was 300\\u20131000\\u202fnm. The PL spectra were recorded using a microspectrometer with a 365\\u202fnm UV light as the excitation source. The electrical characteristics were measured using a Keithley 2400 SourceMeter under simulated AM 1.5 illumination (100\\u202fmW\\u202fcm\\u22122) by a Xenon-lamp based solar simulator. The EL spectra, radiance and EQE were recorded and calculated using a spectrometer (USB2000\\u202f+, Ocean Optics, Shanghai, China) and ISM-Nit software. Photo-stability studies were performed by using a 40\\u202fW Oriel 96000 (Xe) lamp-illuminator as the light source. UV stability test were carried using a 12\\u202fW UV lamp (\\u03bbmax =\\u202f365\\u202fnm).\\n\\nFirst principle calculations were preformed to understand the structure of FA4GeIISbIIICl12. The calculations were realized by using the projected augmented wave plane-wave basis, implemented in the Vienna ab initio simulation package . An energy cutoff of 500\\u202feV is employed and the atom positions are optimized using the conjugate gradient scheme without any symmetric restrictions until the maximum force on each of them is less than 0.02\\u202feV\\u202f\\u00c5\\u22121. The perfect FA4GeIISbIIICl12 was modeled with 4\\u202f\\u00d7\\u202f6\\u202f\\u00d7\\u202f4 grid for the k-point sampling. The generalized gradient approximation exchange-correlation DFT functional Perdew-Burke-Ernzerhof (PBE) with DFT-D3, which includes the dispersion interaction, was employed for the geometric optimization. The electronic-structure calculations were performed using the PBE functional based on the optimized geometries, the XRD was calculated by Reflex module implements in Material Studio.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA4GeSbCl12,\\n Perovskite_composition_short_form: FAGeSbCl,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium (diisopropoxide) bis(2,4-pentanedionate) (TIPD), indium acetate (In(OAc)3, 99.99%), copper iodide (CuI, 99.999%), thiourea (\\u226599.0%), 1-propionic acid (\\u226599.5%), n-Butylamine (\\u226599.0%), Aluminium oxide (Al2O3, 20\\u202fwt% in isopropanol) and silver wire (Ag, 99.999%) were purchased from Sigma-Aldrich. Methylammonium iodide (MAI, \\u226599.5%) and lead iodide (PbI2,\\u226599.9%) were purchased from Xi'an Polymer Light Technology Corp (China). [,]-phenyl-C61-butyric acid methyl ester (PC60BM, 95\\u202fwt %) were purchased from Luminescence Technology Co. ZnO (20\\u202fwt% in isopropanol) was purchased from Aladdin Holdings Group. N,N-dimethyl formamide (DMF, anhydrous) and Dimethyl sulfoxide (DMSO, anhydrous) were used as main solvents. Indium tin oxide-coated glass slides (ITO, \\u226415\\u202f\\u03a9/square) are cleaned before use.\\n\\nITO substrates were first etched by Zn powders and cleaned, then the CuInS2 precursor solution was prepared by dissolving In(OAc)3, CuI, and thiourea in a mixture of n-Butylamine and 1-propionic acid, which was spin-coated onto the ITO films at 2000 r.p.m. for 30\\u202fs. After that, the films were dried at 150\\u202f\\u00b0C for 10\\u202fmin, then heated to 250\\u202f\\u00b0C and held for 15\\u202fmin. More details are described elsewhere []. Al2O3 isopropanol dispersing solution was diluted by isopropanol at a volume ratio of 1\\u20136, then spin-coated on ITO/CuInS2 film at 4000\\u202fr.p.m. for 30s and annealed at 150\\u202f\\u00b0C for 10\\u202fmin to obtain ITO/CuInS2/Al2O3 film. The perovskite precursor using PbI2 was dissolved in mixed solvents of composition DMF: DMSO\\u202f=\\u202f9:1 (v/v) (40% by weight) with a molar ratio of CH3NH3I/PbI2\\u202f=\\u202f1:1, which was spin-coated on the ITO/CuInS2/Al2O3 film. After the first 10\\u202fs of the spin coating process, the ethyl ether solution was quickly dropped at the film. After that, the samples were dried at 100\\u202f\\u00b0C for 5\\u202fmin to form ITO/CuInS2/Al2O3/CH3NH3PbI3 films. Then, the CBZ solution containing PCBM (20\\u202fmg\\u202fmL\\u22121) was spin-coated on ITO/CuInS2/Al2O3/CH3NH3PbI3 films to form ITO/CuInS2/Al2O3/CH3NH3PbI3/PCBM films. Some of these samples were used to prepare ITO/CuInS2/Al2O3/CH3NH3PbI3/PCBM/ZnO:TIPD thin films. ZnO isopropanol dispersing solution was first diluted with anhydrous isopropanol in accordance with the volume ratio of 1:200, then ZnO:TIPD isopropanol solution was prepared by adding 10\\u202f\\u03bcl TIPD solution to 2\\u202fml ZnO isopropanol diluents, which was further spin-coated on the ITO/CuInS2/Al2O3/CH3NH3PbI3/PCBM to obtain ITO/CuInS2/Al2O3/CH3NH3PbI3/PCBM/ZnO:TIPD thin films after drying (at 100\\u202f\\u00b0C for 5\\u202fmin). For the preparation of ITO/CuInS2/Al2O3/CH3NH3PbI3/ZnO:TIPD film without PCBM, the as-prepared ZnO:TIPD isopropanol solution was directly spin-coated on the ITO/CuInS2/Al2O3/CH3NH3PbI3 film. Finally, for the ITO/CuInS2/Al2O3/CH3NH3PbI3/PCBM, ITO/CuInS2/Al2O3/CH3NH3PbI3/PCBM/ZnO:TIPD and ITO/CuInS2/Al2O3/CH3NH3PbI3/ZnO:TIPD films, 100\\u202fnm Ag electrode is evaporated to complete the device structure in a vacuum condition. The effective area for all as-prepared PSCs is 0.04\\u202fcm\\u22122.\\n\\nScanning electron microscopy images were obtained using a scanning electron microscope (SEM) (JSM-7001F, Japan Electron Optics Laboratory Co., Ltd., Tokyo, Japan). The XRD pattern was measured by X-ray diffractometry (DX-2700, Dandong Haoyuan Instrument Company, China). UV\\u2013visible absorption spectra were obtained using a Varian Cary 5000 UV\\u2013vis spectrophotometer. The strady-state photoluminescence (PL) spectra were recorded on the HORIBA Jobin Yvon Fluorolog-3 Spectrofluorometer system. The 510\\u202fnm light is incident form the ITO side as the photon excition Time-resolved fluorescence analyses were measured with an Edinburgh Instrument FLS 980 photoluminescence spectrometer and the time-resolved PL decay is probed at 775\\u202fnm after light excitation. Reconvolution fit analysis was used to fit a measured sample decay to a model function with three exponential terms. The quality of the fit was estimated by the parameter \\u03c72 (0.90\\u2264\\u03c72\\u202f\\u2264\\u202f1.10) and the symmetrical distribution of the residuals about the zero axis. The AFM and conductive atomic force microscopy (c-AFM) tests were performed by Bruker Dimension FastScan Scanning Probe Microscope (SPM). Current density-voltage (J-V) characteristics were collected by the electrochemical workstation (VersaSTAT 3, Ametek, USA) under AM1.5G illumination (100\\u202fmW\\u202fcm\\u22122). The light intensity was calibrated with a NIST-certified silicon reference solar cell (Newport 532 ISO1599). Electrochemical impedance spectroscopy (EIS) was measured under darkness by the CHI660E electrochemical workstation (Chenhua Device Company, Shanghai, China). The measured EIS results were simulated using the Z-view software. All J-V and EIS measurements of as-prepared solar cells without encapsulation were performed in ambient atmosphere (55% relative humidity) at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: CuInS2 | Al2O3-np,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The p-i-n inverted MAPbI3 PSCs were fabricated with a structure of ITO/PTAA/ MAPbI3/PCBM/Bphen/Cu. The fabrication scheme of PSCs are shown in Fig. 1 . Before device fabrication, the ITO substrates were cleaned by ultrasonics in deionized water, acetone, and isopropyl alcohol sequentially for 15\\u2009min. After drying in a N2 flow, the substrates were further treated with UV-ozone for 10\\u2009min, and then the substrates were transferred into a N2-filled glove-box. The hole transport layer PTAA was spin-coated on ITO surface by following the procedure reported previously []. The MAPbI3 film was fabricated by standard antisolvent method as reported by Xiao et al. [] with anhydrous chlorobenzene (CB) as the antisolvent. The precursor is a mixture of PbI2 (550\\u2009mg/ml) and MAI (550\\u2009mg/ml) in a mixed solvent of N,N-dimethylformamide (DMF): dimethyl sulfoxide (DMSO). The precursor solution was then spun onto PTAA at 5000\\u2009r.p.m. and the sample was quickly washed with CB. Subsequently, the sample was annealed at 100 \\u2103 for 20\\u2009min.\\u2009A group of MAPbI3 films was kept in untouched as control samples. The PCBM (20\\u2009mg/ml in CB) solution was coated onto the other MAPbI3 substrates by spin-coating at 1500\\u2009r.p.m. for 10\\u2009s and 3500\\u2009r.p.m. for 35\\u2009s, and annealed at 100 \\u2103 for 30\\u2009min. The devices were finished by thermally evaporating Bphen (\\u223c15\\u2009nm) and copper (\\u223c70\\u2009nm) in sequential order.\\nTo evaluate the light-induced degradation effect, the as-grown devices were put into a glove-box, in which the humidity level and oxygen level are both less than 0.1\\u2009ppm. The devices were aged using a mercury lamp with an illumination intensity of 200\\u2009mW/cm2. The temperature of the samples were monitored during the illumination, and the range is between 25\\u201345 \\u2103. Focused on the short-term degradation, the light exposure times were set as 0, 2, 4, 6, 8 and 13\\u2009h for different batch of devices. Then, the current density\\u2013voltage (J\\u2013V) characteristics of PSCs were measured by a digital Source Meter (Keithley, model 2420) at 300\\u2009mV/s from \\u22121.5\\u2009V to +1.5\\u2009V, and the standard silicon solar cell was employed to calibrate the solar simulator (Newport 91160s, AM 1.5\\u2009G) with a light intensity of 100\\u2009mW/cm2. Furthermore, the Cu electrode and the electron transport layers of Bphen and PCBM were peeled off to expose the layer of MAPbI3 for following examinations. The absorption spectra and crystallographic properties of the perovskite films were characterized by employing an ultraviolet\\u2013visible spectrophotometer (UV\\u2013vis, Puxi, T9) and X-ray diffractometer (XRD, Rigaku D, Max 2500), respectively. The surface roughnesses of MAPbI3 films were obtained by an atomic force microscope (AFM, Agilent Technologies 5500AFM/SPM System) [,]. Ultraviolet photoelectron spectroscopy (UPS, He I, 21.22\\u2009eV) and X-ray photoelectron spectroscopy (XPS, Al K\\u03b1 X-ray source, 1486.6\\u2009eV) were employed to investigate the detailed exposure effects of the devices [].\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Bphen,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Cu,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Cesium iodide (CsI) (99.999%, Sigma-Aldrich), lead iodide (PbI2) (99.999%, Sigma-Aldrich) methyl ammonium bromide (Greatcellsolar), formamidinium iodide (Greatcellsolar), tin chloride dihydrate (SnCl2\\u00b72H2O), (99.99%, Sigma-Aldrich), 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene (spiro-OMeTAD) (99% Lumtec), lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI, Sigma-Aldrich), 4-tert-butylpyridine (TBP) (96%, Sigma-Aldrich), chlorobenzene (99.9%, spectrophotometric grade) and dimethyl sulfoxide (DMSO) (99.7%, Sigma-Aldrich), N,N-dimethylformamide (DMF) (99.8%, Sigma-Aldrich), anhydrous ethanol, FTO glass substrates, respectively.\\n\\nTo prepare the devices, F-doped tin oxide (FTO) substrates were cleaned with deionized water mixed with surfactant and then with acetone and isopropyl alcohol on an ultrasonic bath for 20 minutes each time. SnO2 ETL was spin-coated and annealed at 200 \\u00b0C for 40 minutes. The (Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3) perovskite solution is then prepared in 4:1 ratio of DMF:DMSO. The perovskite layer is spin coated over SnO2 and annealed at 100 \\u00b0C temperature for 30 minutes. Then spiro-OMeTAD doped with Li-TFSI and TBP (Sigma Aldrich), was spin-coated over the perovskite layer. The molar ratios for Li-TFSI and TBP were 0.5 and 3.3. In case of PBDTP-DTDPP polymer, undoped sample of 20% w/w is spin coated whereas for doped samples, TBP and Li-TFSI were used. Finally Au electrodes were thermally deposited by vacuum evaporation (<10\\u22126 torr). For ultrafast measurements, all the layers have been deposited in similar manner on quartz substrate except the electrodes. Current density\\u2013voltage measurement was conducted with a mask in a glovebox under AM1.5 G illumination with an intensity of 100 mW cm\\u22122 (Oriel 1 kW solar simulator) using Keithley 4200. SEM image of film was obtained using Hitachi S-4800.\\n\\nThe cyclic voltammetry (CV) data was obtained by using a PowerLab/AD instrument model system with the working electrode (glassy carbon disk), counter electrode (Pt wire), and reference electrode (Ag/Ag+) at a 50 mV s\\u22121 potential scan speed in a solution of 0.1 M tetrabutylammonium hexafluorophosphate (n-Bu4NPF6)-anhydrous acetonitrile. Film was dropped from a 5.0 mg mL\\u22121 warm CB solution onto the glassy carbon working electrode and dried before measurement under the nitrogen stream. With the use of the ferrocene/ferrocenium redox couple (Fc/Fc+), the potential of the Ag/AgCl reference electrode was internally calibrated. The HOMO energy level was calculated by using the eqn; HOMO = \\u2212(4.80 + Eonset).\\n\\nTransient absorption data were collected using a TAS set-up. TA measurements were performed by using a pump-probe system (UV-VIS HELIOS, Ultrafast systems, Sarasota, FL, USA) and an amplified Ti:sapphire laser. The output of amplified Ti:sapphire laser provides 800 nm fundamental pulses at a 1 kHz repetition rate which were split into optical beams to generate pump and probe pulses. One fundamental beam was used to generate pump beam using an optical parametric amplifier (OPA) system. A white light and near infrared probe was generated by focusing another fundamental beam into a flint glass. Pump and probe beams were focused on a sample and a probe light was collected by a CCD. The instrument response function was \\u223c100 fs full width at half maximum. The pump wavelength was tuned to 500 nm, produced by an optical parametric amplifier (TOPAS-prime, Light conversion, Lithuania), and the differential change in transmission was detected in the probe range 500 to 1500 nm at several time delays.\\n\\nThe TCSPC method was used to record the photoluminescence lifetime profiles of the perovskite incorporated PBDTP-DTDPP polymer and spiro-OMeTAD HTL films. The light source for excitation was the home-built OPO laser. The output of the home-built OPO running in the near infrared region was doubled to generate the excitation pulses at 550 nm. The repetition rate was 500 kHz. A singlet lens was used to focus the excitation pulse onto the sample and the fluorescence was collected with a parabolic mirror. The fluorescence was dispersed with a monochromator, and detected with a single photon detection module. The FWHM of the IRF was 60 ps. Magic angle detection was used to prevent the effects of polarization. All measurements were performed at ambient temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.16MA0.79PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: PBDTP-DTDPP,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: ,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The NH2CHNH2PbI3 (FAPbI3) based perovskite solar cell with the device structure of ITO/PEDOT:PSS/FAPbI3/PCBM/BCP/Ag (Fig. 1) was fabricated according to the following steps. Firstly, pre-cleaned ITO-coated glass substrates were treated by ultraviolet-ozone for 15 min. The poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS, Clevious AI 4083) layer was deposited by spin-coating at 4000 rpm for 40 s and annealed at 140 \\u00b0C for 15 min in air. Then the substrates were transferred into a nitrogen filled glovebox. The FAPbI3 precursor solution (40 wt%), prepared by dissolving NH2CHNH2I (Xi'an Polymer Light Technology Corp.) and PbI2 (Alfa Aesar) in N,N-dimethylformamide (DMF) solvent with a molar ratio of 1:1, was spin coated on the PEDOT:PSS layer following the fast deposition crystallization procedure as previously reported. Then the FAPbI3 precursor solution was annealed to form black FAPbI3 perovskite. After cooling down to room temperature, PC60BM (20 mg ml\\u22121 in chlorobenzene) was spin-coated on the perovskite layer at 2000 rpm, followed by drop casting an interfacial layer solution of BCP (0.5 mg ml\\u22121 in anhydrous ethanol) at 4000 rpm without further annealing. Finally, devices were transferred into the thermal evaporation system (OMV-FS300) for silver cathode evaporation. The active area of the devices (7.25 mm2) was defined through a shadow mask. The MAPbI3-based solar cell with the same device structure was also fabricated for comparison.\\n\\nCurrent density\\u2013voltage (J\\u2013V) characteristics of perovskite solar cells were measured in air using a programmable Keithley 2400 source meter under AM 1.5G solar irradiation at 100 mW cm\\u22122 (Newport, Class AAA solar simulator, 94023A-U). The light intensity was calibrated by a certified Oriel Reference Cell (91150 V) and verified with an NREL calibrated Hamamatsu S1787-04 diode. The external quantum efficiency (EQE) was measured by a certified IPCE instrument (Zolix Instruments, Inc., Solar Cell Scan 100). The scanning electron microscope (SEM) images were obtained from a field emission scanning electron microscope (FEI Quanta 200). The ultraviolet-visible spectroscopy (UV-vis) spectra were achieved on a Perkin Elmer model Lambda 750 instrument. X-ray diffraction (XRD) patterns were collected on an analytical (Empyrean) apparatus. The steady-state photoluminescence spectra and time-resolved photoluminescence were measured by utilizing Horiba Jobin-Yvon LabRAM HR800 and a single photon counting spectrometer, which was combined with the Fluorolog-3 spectrofluorometer (Horiba-FM-2015), respectively. A 625 nm laser source was used in the time resolved PL measurement.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 140,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0725,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Diaquabis(oxoacetato-O,O\\u2032\\u2032)germanium [Ge(C2H2O3)2(H2O)2] was prepared by adding germanium dioxide (0.52 g, 5 mmol) to an aqueous solution (100 mL) of glycolic acid (1.52 g, 20 mmol) and refluxing the acidic mixture at 115 \\u00b0C for 1 h. Then the mixture was concentrated using a rotary evaporator. The obtained colorless crystals were collected and then transferred to a vacuum drying oven at 100 \\u00b0C for 2 days (for convenience, the product is denoted as Ge-gly). A typical synthetic procedure of CGS NCs is briefly described below. First, 1.5 mmol copper(II) chloride dihydrate, 0.75 mmol Ge-gly and 10 mL oleylamine were mixed at room temperature and cycled between vacuum and nitrogen three times in a 100 mL three neck flask connected to a Schlenk line. Afterward, the mixture was kept at 120 \\u00b0C under vacuum for 40 min with stirring and then the temperature was raised to 210 \\u00b0C (solution A). 4 mL oleylamine and 2.25 mmol S powder were mixed in a separate round flask at 150 \\u00b0C under vacuum. When the S powder was completely dissolved, the mixture was then cooled to room temperature (solution B). Finally, solution B was injected into solution A under vigorous stirring and the reaction was maintained for 20 min. The mixture was cooled to \\u223c100 \\u00b0C, followed by adding 5 mL toluene and 40 mL isopropanol. The nanocrystals were collected by centrifugation at 5000 rpm for 10 min. The supernatant, which contained the unreacted precursor and byproducts, was discarded. The precipitate was washed again with 7.5 mL toluene and 45 mL isopropanol to remove the excess oleylamine from CGS NPs.\\n\\nMethylammonium iodide was synthesized by reacting 17.4 mL methylamine (40 wt% in water) and 16.6 mL hydroiodic acid (57 wt% in water) in a 250 mL round bottom flask at 0 \\u00b0C for 2 h with stirring. After the reaction, the white solid of MAI was recovered by rotary evaporation and then washed with diethyl ether and recrystallized twice with ethanol. The CH3NH3I powder was collected and dried at 50 \\u00b0C in a vacuum oven for 24 h. To prepare the perovskite precursor solution, CH3NH3I and PbI2 (Aldrich) were dissolved in a mixed solvent of anhydrous N,N-dimethylformamide (DMF) and dimethylsulfoxide (DMSO) (7:3 in volume) in 1 M concentration. The solution was stirred overnight at 60 \\u00b0C and filtered with 0.22 \\u03bcm PVDF filters before spin-coating.\\n\\nPrior to the deposition of the TiO2 compact layer, the FTO substrate (15 \\u03a9 sq\\u22121) was etched with zinc powder and 2 M HCl to obtain the desired pattern. The etched FTO substrate was sequentially cleaned by ultrasonication in acetone, isopropanol and de-ionized water for 40 min each and then treated in a UV/O3 cleaner for 20 min. A dense TiO2 blocking layer of ca. 40 nm thickness was spin-coated onto FTO with a mixture solution of 140 \\u03bcL of titanium isopropoxide, 2 mL of ethanol, and 26 \\u03bcL of HCl (2 M) at 2000 rpm for 40 s, followed by annealing at 500 \\u00b0C for 1 h in a muffle furnace. To deposit perovskite films, the CH3NH3PbI3 solution (18 \\u03bcL) was first dropped onto a TiO2 coated FTO substrate (1.5 cm \\u00d7 2 cm). The substrate was then spun at 4000 rpm for 30 s. During this process, anhydrous chlorobenzene (100 \\u03bcL) was quickly dropped onto the center of the substrate twelve seconds ahead of the end of rotation. Subsequently, the obtained films were then dried at 60 \\u00b0C for 30 s and further annealed at 100 \\u00b0C for 10 min to form crystallized MAPbI3. To complete the fabrication of devices, two hole transporting materials (spiro-OMeTAD and CGS) were spin-coated onto the perovskite films, separately. For the deposition of the spiro-OMeTAD HTL, 73.2 mg spiro-OMeTAD was first dissolved in 1 mL chlorobenzene, and then 28.8 \\u03bcL 4-tert-butyl pyridine and 18.8 \\u03bcL Li-TFSI solution (520 mg Li-TFSI in 1 mL acetonitrile) were added. The as-prepared spiro-OMeTAD solution was spin-coated onto the CH3NH3PbI3 films at 3000 rpm for 30 s. For the deposition of the CGS HTL, the synthesized CGS NPs were dispersed in 1-hexanethiol to form a stable ink with a concentration of 200 mg mL\\u22121. The CGS NP ink was then spin-coated onto the perovskite films at various speeds for 30 s. In the experiment, we adopt a facile method to control the thickness of CGS by changing the spin speed. When the spin speed was increased from 1000 rpm to 7000 rpm with a step of 1000 rpm, the thickness of CGS decreased from 390 nm to 60 nm. After that, the films were transferred into a heated vacuum chamber placed in a glove box to remove the solvent. Finally, device fabrication was completed by thermally evaporating 80 nm of gold layer with a mask (well-defined area size of 0.12 cm2).\\n\\nThe crystal structure characterization of MAPbI3 and CGS thin films was conducted using an X-ray diffractometer (XRD, D/Max-rA) with Cu-K\\u03b1 radiation (\\u03bb = 1.5406 \\u00c5). The Raman spectra of CGS films were recorded at room temperature using a LABRAM-HR micro-Raman system in the back-scattering configuration with laser sources of 514 nm. The surface morphology and elemental composition were determined by field emission SEM (FE-SEM Sirion 200). Steady-state photoluminescence was measured using a LabRamHR system with excitation at 514 nm. AFM measurements were performed on an XE-7 scanning probe microscope in non-contact mode (Park systems, Korea). The optical absorption spectrum was recorded on a UV-vis-365-type spectrophotometer in the range of 200\\u20131600 nm. Contact angles were measured using a CAM instrument (Data-Physics, Germany). The current density\\u2013voltage (J\\u2013V) characterizations were conducted using a Keithley 2400 source measurement unit under simulated AM1.5 irradiation (100 mW cm\\u22122) with a standard xenon-lamp-based solar simulator (Oriel Sol 3A, USA), and the solar simulator illumination intensity was calibrated using a monocrystalline silicon reference cell (Oriel P/N 91150 V, with KG-5 visible color filter) calibrated by the National Renewable Energy Laboratory (NREL). Time-resolved photoluminescence (TRPL) spectra were obtained using the time-correlated single-photon counting technique (TimeHarp 260) under excitation provided by picosecond pulsed sources (PicoQuant Solea) at a wavelength of 540 nm with a repetition frequency of 2.5 MHz. All the samples were excited from the glass side. The data were fitted with biexponential functions of the form A1exp(\\u2212t/\\u03c41) + A2exp(\\u2212t/\\u03c42) + B, where A1 and A2 are prefactors and \\u03c41 and \\u03c42 are time constants.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60; 100,\\n Perovskite_deposition_thermal_annealing_time: 0.33; 10.0,\\n HTL_stack_sequence: CGS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Large area single-layer graphene was synthesized on 70\\u202f\\u03bcm Cu foil by chemical vapor deposition at 1000\\u202f\\u00b0C under flow of CH4 (30 sccm) as a carbon source and H2 (10 sccm) as a reduction gas at a pressure of 10\\u202fTorr. After the growth of graphene on the Cu foil, poly(methyl methacrylate) (PMMA) solution was drop-coated onto the graphene sheet/Cu foil at 5000\\u202frpm for 60\\u202fs and then annealed at 180\\u202f\\u00b0C for 1\\u202fmin. The Cu foil was etched away using an FeCl3 etchant for 2\\u202fh to obtain a PMMA-coated graphene film. Then, the PMMA layer was removed in an acetone bath for 1\\u202fh to obtain a graphene sheet on PET substrate. These steps were repeated up to four times to obtain single to quadruple layers of graphene (named as 1LG to 4LG) on PET substrates, based on layer-by-layer stacking method [].\\n\\nThe topological images of graphene layers for L n from 1 to 4 were obtained by using noncontact-mode atomic force microscope (AFM) (Park System XE-100). Raman spectra of the graphene sheets were obtained with a micro-Raman spectroscopy system. 532-nm laser was used as the excitation source with a power of \\u223c1\\u202fmW. Ultra-violet-visible transmittance spectra were recorded on a Varian Cary-5000 spectrophotometer in the wavelength range of 300\\u2013900\\u202fnm. Sheet resistance and work function were measured by 4-probe method (Dasol eng, model FPP-HS8-40K) and Kelvin-probe force microscope (Park System XE-100), respectively. The calibration of the work function was done by using gold as a reference. L n-dependent behaviors of electron mobilities were analyzed by Hall-effect measurements (Ecopia model HEM-2000).\\n\\nPEDOT:PSS (Clevios P VP Al 4083) was spin-coated on ITO or graphene/PETs at 3000\\u202frpm for 40\\u202fs and then annealed at 140\\u202f\\u00b0C for 20\\u202fmin. For the perovskite layer, solution of CH3NH3PbI3 (MAPbI3) was prepared by dissolution of 1:1 ratio of methyl ammonium iodide powder (Dye sol) and lead(II) iodide powder (Aldrich) in \\u03b3-butyrolactone:dimethyl sulfoxide mixed solvent (7:3, volume ratio) at 60\\u202f\\u00b0C. The fully-dissolved solution was spin-coated onto the PEDOT:PSS layer by two consecutive spin-coating steps at 1000 and 4000\\u202frpm for 20 and 60\\u202fs, respectively. During the second spin-coating step, 350\\u202f\\u03bcL toluene was quickly dropped onto the rotating substrate and subsequently dried at 100\\u202f\\u00b0C for 5\\u202fmin. After that, 2% PCBM in chlorobenzene solution was coated onto the perovskite layer at 2000\\u202frpm for 60\\u202fs. Finally, the device was transferred to a vacuum chamber for Al-electrode evaporation.\\n\\nCross-sectional structural images of the perovskite solar cells were obtained by field-emission scanning electron microscopy (FE-SEM) (Carl Zeiss, model LEO SUPRA 55). Current density-voltage (J\\u2013V) characteristics of the solar cells were measured by solar simulator (McScinece K201) under illumination of 1 Sun (100\\u202fmWcm\\u22122, AM 1.5G). For measuring the hysteresis of the J\\u2013V curves, the forward and reverse scan rate was set to 200 ms/10\\u202fmV. The active area of all devices was defined as 0.16\\u202fcm2. The J-V curves were measured in the central circular region of 0.096\\u202fcm2 active area with the remaining edge part masked. External quantum efficiency (EQE) was measured under monochromatic light generated by a Xenon arc-lamp (Oriel Apex Illuminator, Newport) in combination with a monochromator (Cornerstone 260, Newport). The light was chopped and the current response of the sample was detected by a lock-in amplifier (SR810, Stanford Research Systems). The calibration of the setup was done by measuring a silicon reference diode with known spectral response. The light-soaking experiment was performed under illumination of 1 Sun using a 420\\u202fnm UV light cut\\u2013off filter under room temperature. Bending tests of the flexible TCEs and solar cells were done at 0.5\\u202fHz bending frequencies at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.096,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Mini-modules manufactured with CH3NH3PbI3 (MAPI) and Cs0.05FA0.83MA0.17PbI(0.87Br0.13)3 (FMC) perovskite mini-modules were used in this work (Solaronix, 2018). The final manufactured modules were 5\\u202fcm\\u202f\\u00d7\\u202f5\\u202fcm in size and consist of five serially connected cells with 2.7\\u202fcm2 per cell and 13.5\\u202fcm2 total active area, device geometric fill factor was 0.54.\\nBoth MAPI and FMC were prepared from solution on ITO-coated glass (7\\u03a9/sq). A NiOx hole transport layer is obtained by spin coating a solution of 0.22\\u202fM nickel acetate tetrahydrate dissolved in a 1:0.012\\u202fvol ratio of 2-methoxyethanol:ethanolamine at 3500\\u202frpm for 30\\u202fs. The formed layer was annealed at 250\\u202f\\u00b0C for 60\\u202fmin before cooling to room temperature. The MAPI precursor solution was prepared by dissolving 576\\u202fmg PbI2 and 199\\u202fmg MAI in 0.8\\u202fml DMF and 0.2\\u202fml DMSO. The FMC solution was prepared by dissolving PbI2 (0.35\\u202fg), FAI (0.12\\u202fg), MAI (0.035\\u202fg), CsI (0.026\\u202fg) and PbBr2 (0.09\\u202fg) in 0.8\\u202fml of DMF and 0.2\\u202fml DMSO. Both structures were deposited using a one-step method using ethyl acetate as antisolvent. The electron transport layer used in this work was PC60BM, spin coated from a 20\\u202fmg/ml solution in chlorobenzene at 2000\\u202frpm for 30\\u202fs. A bathocuproine (BCP) (0.5\\u202fmg/ml in anhydrous ethanol) contact layer was spin-coated at 6000\\u202frpm for 15\\u202fs. Finally, 100\\u202fnm Ag contacts were added by thermal evaporation. For module patterning, the P1 was defined by laser scribing of the substrate ITO, P2 was scribed using a scalpel blade, and P3 was defined by evaporating the electrode metal though a shadow mask. Finally, a light curable epoxy (Ossila) and a thin glass cover were used for encapsulation. Wires were soldered to the Ag contacts and then covered by a UV-curable epoxy (Threebond) which acted as edge sealant.\\n\\nSix modules were tested for this work and bonded to the centre of a 205\\u202fmm\\u202f\\u00d7\\u202f160\\u202fmm glass backplane and were covered with a commercially available UV filter (Solaronix, 2018) which filters the UV component of sunlight. Data is presented for the median device. After the UV filter was added, the final stage of the encapsulation was concluded by sealing the edges of the modules with low temperature two part fast curing sealing epoxy supplied by Dyesol UK ltd (now Greatcell Solar Ltd.) (Dyesol).\\nFor this experiment, all modules were initially tested indoors using a Newport 94021A class ABB standard AM1.5G solar simulator, to ensure that all devices showed consistent performance prior to outdoor testing. The modules were then laminated onto glass substrates and covered with a UV filter before being retested. The average device photovoltaic performance of each type was as follows: MAPI - short-circuit density (JSC)\\u202f=\\u202f2.38\\u202fmA/cm2, open-circuit voltage (VOC)\\u202f=\\u202f5.20\\u202fV, fill factor (FF)\\u202f=\\u202f39.9%, power conversion efficiency (PCE)\\u202f=\\u202f4.92%; FMC\\u202f\\u2212\\u202fJSC\\u202f=\\u202f2.55\\u202fmA/cm2, VOC\\u202f=\\u202f5.40\\u202fV, FF\\u202f=\\u202f43.0%, PCE\\u202f=\\u202f5.92%.\\n\\nThe outdoor experiments were performed over two campaigns in April and June 2017 at the School of Electronics, Bangor, Gwynedd, North Wales at coordinates latitude 53.228\\u00b0N, longitude \\u22124.129\\u00b0W and altitude approximately 20\\u202fm above sea level. The performance monitoring of the poly-Si module is conducted using a PVMS250 PV measurement system (Egnitec, UK) and the perovskite mini-modules were measured using a Botest SMU. The poly-Si modules are kept at maximum power point in between periodic current-voltage (IV) sweeps (once every minute). Each module has a PT100 temperature sensor fixed to its backplane. Current and voltage at the maximum power point (IMPP, VMPP) and temperature measurements are taken every 15\\u202fs. The perovskite mini-modules were kept at open-circuit between IV sweeps conducted once every 15\\u202fmin. All mini-modules also had PT100 sensors constantly reading the module temperature. For these tests, all monitored modules were mounted in-plane towards the sun at an angle of 36\\u00b0 (the optimum for this latitude).\\nDuring the outdoor testing, the incident irradiance was monitored using IMT silicon solar reference cells. The weather conditions were constantly recorded using a dedicated weather station setup. The outdoor measurement setup conforms to the ISOS-O2 outdoor measuring protocol (Reese et al., 2011). The data were analysed using a combination of MySQL, MS Access, and MS Excel.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 85,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: NiO,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 13.5,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: TRUE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Chlorobenzene (CB), CsI, PbI2, 2-methoxyethanol, CuSCN, diethyl sulfide, and 1,4,7,10,13,16-hexaoxacyclooctadecane (18-crown-6, shortly denoted as Crown) were purchased from Alfa Aesar. Zinc acetate, thiourea, monoethanolamine, ethanol, acetonitrile, N-methyl-2-pyrrolidone (NMP), N,N-dimethylformamide (DMF), hydriodic acid (HI) (49% in water) and isopropanol (IPA) were purchased from Sinopharm Chemical Regent Co., Ltd. TiO2 paste and Spiro-OMeTAD were purchased from Xi'an Polymer Light Technology in China.\\n\\nCsI\\u2013Crown was synthesized by reacting 260 mg CsI, 264 mg Crown and 20 mL ethanol in a 250 mL beaker at room temperature for 3 hours with stirring. The white solids were gradually precipitated. The precipitate was recrystallized using diethyl ether, and finally dried at 100 \\u00b0C in a vacuum oven for 48 hours to fully remove water.\\n\\nCsPbI3\\u00b7Crown crystals were synthesized by reacting 260 mg CsI, 461 mg PbI2 and 26 mg Crown in a 250 mL beaker at 170 \\u00b0C for 10 hours while stirring. Needle-like crystals were gradually grown. Then, the precursor solution was filtered away to collect the CsPbI3\\u00b7Crown crystals. The crystal was resolved by single-crystal X-ray diffraction as shown in Fig. S7.\\u2020 CCDC 1978630.\\n\\nThe PbI2\\u00b7NMP compound was synthesized according to a previously report method. Briefly, PbI2 and NMP (equal molar quantity) were stirred in a 100 mL beaker at 0 \\u00b0C for 1 day. The PbI2\\u00b7NMP precipitate was collected, and then recrystallized using diethyl ether, and finally dried at 120 \\u00b0C in a vacuum oven for 48 hours.\\n\\nA compact ZnO\\u2013ZnS electron transporting layer (ETL) was deposited onto cleaned FTO glass (NSG, Tec-7) following a previously reported method. First, a compact ZnO ETL was spray-coated onto the hot FTO substrate using 0.37 M zinc acetate and monoethanolamine (molar ratio 1:1) in ethanol solution at 400 \\u00b0C for 30 min. Second, the FTO with the ZnO ETL was immersed into an ethanol solution of thiourea (76 mg mL\\u22121) at 70 \\u00b0C for 10 min, and then annealed in air at 400 \\u00b0C for 30 min to obtain the ZnO\\u2013ZnS ETL. A mesoporous TiO2 film was deposited on the ZnO\\u2013ZnS/FTO substrate by spin-coating TiO2 paste (1:5, mass ratio) at 5000 rpm for 20 s, and annealed at 400 \\u00b0C for 30 min. For the CsPbI3 perovskite layer, a mixture solution of 1.0 mmol PbI2\\u00b7NMP compound and 1.0 mmol CsI in 1 mL DMF with an additive (30 \\u00b5L HI) was spun onto the substrates at 4000 rpm for 30 s, and then 100 \\u00b5L CB was dropped on the spinning substrate 10 s prior to the end of the process. Finally, the substrate with the CsPbI3 film was heated at 170 \\u00b0C for 30 min. For the Crown passivation process, the Crown solution was prepared by dissolving 1 mg Crown in 1 mL of IPA, and then dripped on the CsPbI3 film (4000 rpm, 30 s). Finally, the above substrate was heated at 100 \\u00b0C for 10 min. After preparation of the CsPbI3 film, a 20 \\u00b5L drop from the CB solution (each milliliter containing 73.2 mg Spiro-OMeTAD, 8.6 \\u00b5L of Li-TFSI/acetonitrile (520 mg mL\\u22121) and 14.4 \\u00b5L of TBP) was coated via the solution process at 4000 rpm for 10 s to get the hole transport layer (HTL). The fabrication process of the inorganic HTL, CuSCN, was carried out in accordance with reported work. First, the CuSCN solution was prepared by dissolving 20 mg CuSCN in 1 mL of diethyl sulfide after continuous stirring at 40 \\u00b0C for 50 min, and then dripped within 5 s on the perovskite substrate spinning at 4000 rpm. Finally, the above substrate was heated at 50 \\u00b0C for 30 min. Finally, 60 nm of Au was prepared via thermal evaporation. The active area was defined by a 0.1 cm2 mask. The perovskite deposition was carried out in a homemade glovebox under controlled atmospheric conditions by using compressed dry air to recirculate ventilation and purify the fabrication atmosphere. After several recirculating purification, the relative humidity could be retained at a value about 10\\u201315%.\\n\\nThe module consisting of four sub-cells connected in series was scribed using a laser engraving machine (ZNL1810V2, Hangzhou Zhongneng Optoelectronic Technology Co., Ltd., China). For fabrication of PSC modules, three laser-patterning lines, P1 (500 \\u00b5m), P2 (250 \\u00b5m), and P3 (350 \\u00b5m) were accomplished by a laser with a power of 18 W, 10 W and 7 W, respectively. The active area of PSC modules was calculated to be 8.0 cm2 without the mask. For the spin coating of large-area CsPbI3 perovskite films, all procedures were consistent with the small-cell case by the same method. For the blade coating of CsPbI3 perovskite films, a 4 \\u00b5L droplet of CsPbI3 precursor was added into the gap (\\u223c200 \\u00b5m) between the blade and substrate, and then the blade was moved on with a speed of \\u223c200 mm s\\u22121. Next, the wet films were transferred into a vacuum chamber in a short time, and quickly pumped to \\u223c10\\u22122 Pa from atmospheric pressure within 15 s, and then maintained for 1 min at this pressure. After the vacuum-flash process, the substrate was transferred to a hotplate for 30 min annealing at 170 \\u00b0C. For the Crown passivation process, 5 \\u00b5L of Crown/IPA solution (1 mg mL\\u22121) was loaded in the gap (around 100 \\u00b5m) between the blade and the CsPbI3 surface, and the blade was moved at a speed of \\u223c50 mm s\\u22121. Then the above substrate was annealed on a hotplate at 100 \\u00b0C for 10 min. The perovskite deposition was carried out in a homemade glovebox under controlled atmospheric conditions with relative humidity 10\\u201315%. All procedures were consistent with the small-cell case.\\n\\nThe Maximum-power-point (MPP) of the encapsulated module was determined by the J\\u2013V scan using a Keithley 2400 source meter under AM 1.5 simulated solar irradiation (white LED light, LSH-7320, Newport) and the Vmax was obtained at the corresponding maximum power point (MPP) for the device. In the MPP tracking, a bias voltage equal to the Vmax was applied on the device to simulate the max-power-output for the device to evaluate the operation stability. The storage conditions during operation were maintained at 25 \\u00b0C by a Peltier element and a relative humidity of 60%.\\n\\nThe J\\u2013V characteristics of PSCs were analyzed on a solar simulator (Newport, Class 3A, 84023A) under AM 1.5 G standard light (100 mW cm\\u22122) equipped with a Keithley 2400 source meter. The IPCE spectra were measured on an IPCE system (Newport) equipped with a Xenon lamp (66920, Newport, 300 W xenon lamp), a monochromator (Cornerstone 260, Newport) and a power meter (2936-R, Newport). The perovskite films were analyzed on an X-ray diffractometer (Rigaku, SmartLab-SE) with a Cu K\\u03b1 radiation source. Surface and cross-sectional morphologies and EDS maps of the perovskite films were obtained on a field-emission scanning electron microscope (SEM) (ZEISS, Sigma). The UV-vis spectra were recorded on a UV-2550 UV-vis spectrophotometer. IR spectra were collected on an infrared spectrometer instrument (Thermo Fisher, Nicolet iS50). The trap state density of perovskite films, CsPbI3 and CsPbI3\\u2013Crown films, with the typical configuration (FTO/perovskite/Au) was evaluated using the space-charge-limited current (SCLC) model. The steady and time-resolved PL spectra were measured using an FLS980 (Edinburgh) fluorescence spectrometer excited by a 377.6 nm pulsed laser. PL mapping measurements were performed on a laser Raman microscope (RAMAN-11, Nanophoton). Kelvin probe force microscopy (KPFM) of perovskite films with surface potential and topography characteristics was performed on an atomic force microscope equipped with a controller using a Pt/Ir-coated Si tip. Water contact angles were measured on an optical contact-angle meter system. The 133Cs solid-state MAS (magic angle spinning) NMR spectra were collected on a Bruker Avance III 400 MHz NMR spectrometer with a 4.0 mm probe under spinning rates from 12 kHz at room temperature (298 K). The diffraction data of CsPbI3\\u00b7Crown were collected on an Agilent SuperNove X-ray single crystal diffractometer using Cu K\\u03b1 (\\u03bb= 1.54184 \\u00c5) micro-focus X-ray sources at 100 K.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO-c | TiO2-mp,\\n ETL_additives_compounds: nan | Thiourea,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating >> Dipp-coating,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 170,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: 18-crown-6 ether | Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25; 25,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 2000,\\n Stability_PCE_initial_value: 13.03,\\n Stability_PCE_end_of_experiment: 30,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A schematic illustration of the fabrication process of the perovskite photovoltaic cells is shown in Fig. 1. F-Doped tin oxide (FTO) substrates were cleaned in an ultrasonic bath with acetone and methanol and then dried under nitrogen gas. The TiO2 (0.15 M and 0.30 M) precursor solutions were prepared from titanium diisopropoxide bis(acetyl acetonate) (Sigma-Aldrich, Tokyo, Japan, 0.055 and 0.11 mL) with 1-butanol (1 mL). The 0.15 M TiO2 precursor solution was spin-coated on the FTO substrate at 3000 rpm for 30 s and the coated substrate was then annealed at 125 \\u00b0C for 5 min. Then, the 0.30 M TiOx precursor solution was spin-coated on the TiO2 layer at 3000 rpm for 30 s and the resulting substrate was annealed at 125 \\u00b0C for 5 min. The process for forming the 0.30 M precursor layer was performed twice. Then, the FTO substrate was sintered at 550 \\u00b0C for 30 min to form a compact TiO2 layer. To form the mesoporous TiO2 layer, a TiO2 paste was prepared from the TiO2 powder (Aerosil, Tokyo, Japan, P-25) with poly(ethylene glycol) (Nacalai Tesque, Kyoto, Japan, PEG #20000) in ultrapure water. The solution was mixed with acetylacetone (Wako Pure Chemical Industries, Osaka, Japan, 10 \\u03bcL) and surfactant (Sigma-Aldrich, Triton X-100, 5 \\u03bcL) for 30 min and was then allowed to stand for 24 h to remove bubbles from the solution. Then, the TiO2 paste was spin-coated on the compact TiO2 layer at 5000 rpm for 30 s. The resulting cell was heated at 125 \\u00b0C for 5 min and then annealed at 550 \\u00b0C for 30 min to form the mesoporous TiO2 layer.\\nTo prepare the perovskite compounds, mixed solutions of CH3NH3I (2.4 M, Showa Chemical, Tokyo, Japan), PbCl2 (0.8 M, Sigma-Aldrich) and PbI2 (0.08 M, Sigma-Aldrich) in DMF (Sigma-Aldrich, 500 mL) were prepared for the standard cell. Details of the perovskite solutions with CuBr2 and alkali metal elements are listed in Table S1.\\u2020 These perovskite solutions were then introduced into the TiO2 mesopores by spin coating at 2000 rpm for 60 s, followed by annealing at 140 \\u00b0C for 10 min in ambient air.\\nThen, a hole-transport layer was prepared by spin coating; a solution of spiro-OMeTAD (Wako Pure Chemical Industries, 50 mg) in chlorobenzene (Wako Pure Chemical Industries, 0.5 mL) was mixed with a solution of lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI; Tokyo Chemical Industry, Tokyo, Japan, 260 mg) in acetonitrile (Nacalai Tesque, 0.5 mL) for 24 h. The former solution with 4-tert-butylpyridine (Sigma-Aldrich, 14.4 \\u03bcL) was mixed with the Li-TFSI solution (8.8 \\u03bcL) for 30 min at 70 \\u00b0C. Then, the spiro-OMeTAD solution was spin-coated on the perovskite layer at 4000 rpm for 30 s. All procedures were performed in air.\\nFinally, gold (Au) electrodes were evaporated as top electrodes using a metal mask for the patterning. Layered structures of the prepared photovoltaic cells are denoted as FTO/TiO2/perovskite/spiro-OMeTAD/Au. The prepared perovskite photovoltaic devices were stored at 22 \\u00b0C and \\u223c30% humidity.\\n\\nJ\\u2013V characteristics of the photovoltaic cells were measured under illumination at 100 mW cm\\u22122, with the use of an AM 1.5 solar simulator (San-ei Electric, XES-301S). J\\u2013V measurements were performed using a source measurement unit (Keysight, B2901A Precision SMU). The scan rate and sampling time were \\u223c0.08 V s\\u22121 and 1 ms, respectively. Four cells were tested for each cell composition and the reported values are the averages of these four measurements (\\u03b7ave). The solar cells were illuminated through the sides of the FTO substrates and the illuminated area was 0.0784 cm2. EQEs (Enli Technology, QE-R) of the cells were also measured using a source meter (Keithley Tektronix, 2450). The microstructures of the cells were investigated by X-ray diffraction (XRD, Bruker, D2 PHASER) and scanning electron microscopy (SEM, JEOL, JSM-6010PLUS/LA) equipped with energy dispersive X-ray spectroscopy (EDS).\\n\\nThe electronic structures of the perovskite crystals were calculated for the single-point with the experimental parameters obtained from XRD, through ab initio quantum calculations based on the unrestricted Hartree\\u2013Fock (HF) method. We used density functional theory (DFT) and the Perdew\\u2013Burke\\u2013Ernzerhof (PBE)-based hybrid function and unrestricted B3LYP (UB3LYP) with LANL2MB as the basis set (Gaussian 09). The metal-incorporated MAPbI3 cubic structures were treated as a cluster model with supercells of 2 \\u00d7 2 \\u00d7 2 fixed to have a positive charge of +8. A lattice constant of 6.391 \\u00c5 was used for the perovskite compounds with a cubic crystal system. The numbers of quantum spins in the metal (M)-incorporated MAPbI3 and MAPbI3 crystals were assumed to be doublet (S = 1/2) states at M = Cu2+ and a singlet (S = 0) state at M = Pb2+, respectively. As an isolated dilution system, the mole ratio of the transition metal to Pb metal was adjusted to be 1:26. The concentration of the metal atom was maintained at less than 5% so as not to break crystal symmetry by suppression of strong exchange interactions in the perovskite crystal. Alkali metal elements (i.e., Na+, K, Rb+, and Cs+) were substituted for MA+ sites at contents of less than 12%. We calculated the total and partial DOS (TDOS and pDOS), the occupancy of the 3d orbital on the transition metal, 6s, 5p, and 6p orbitals of the I and Pb atoms around the highest occupied molecular orbital (HOMO), and lowest unoccupied molecular orbital (LUMO), and the HOMO\\u2013LUMO energy gap (Eg). The vibration modes in infrared spectroscopy (IR) spectra were also calculated by DFT using the frequency mode. The Gibbs energy (G) and enthalpy (H) were obtained by the IR calculation, and the entropy was calculated by using G = H \\u2212 TS, where T is 298 K.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: CuBr2; RbI,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 140,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 22.0; 22.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1176,\\n Stability_PCE_initial_value: 12.5,\\n Stability_PCE_end_of_experiment: 104,\\n Cell_area_measured: 0.0784,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were purchased as following: Lead (\\u2161) iodide (PbI2, ultra dry, 99.999%, Alfa Aesar), 1-octadecene (ODE, technical grade 90%, Sigma Aldrich), oleic acid (OA, technical grade 90%, Alfa Aesar), oleylamine (OLA, technical grade 70%, Sigma Aldrich), cesium carbonate (Cs2CO3, 99.99%, Alfa Aesar), methyl acetate (MeOAc, extra pure grade \\u226599.5%, Duksan), n-hexane (anhydrous, Alfa Aesar), n-octane (extra pure Alfa \\u226599%, Acros Organics), TiO2 precursor solution (SC-BT060, Sharechem), TiCl4 aqueous solution (Sharechem), lead (\\u2161) nitrate (Pb(NO3)2, 99.999%, Sigma Aldrich), lead (\\u2161) acetate trihydrate (Pb(OAc)2\\u00b73H2O, 99.995%, Alfa Aesar), sodium acetate (NaOAc, 99.995%, Sigma Aldrich), cesium acetate (99.998%, Alfa Aesar), formamidinium iodide (FAI, GreatcellSolar), ethyl acetate (EtOAc, extra pure grade \\u226599.5%, Duksan), 2,2\\u2032,7,7\\u2032-Tetrakis(N,N-di-p-methoxyphenylamine)-9,9\\u2032-spirobifluorene (spiro-MeOTAD, \\u226599.5%, Lumtec), chlorobenzene (anhydrous, 99.8%, Sigma Aldrich), lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI, \\u226598%, Alfa Aesar), acetonitrile (anhydrous, 99.8%, Sigma Aldrich), 4-tert-butylpyridine (4-TBP, 96%, Sigma Aldrich) and 2-amylpyridine (\\u226598.0%, TCI). Phenyl-C61-butyric acid methyl ester (PCBM) was purchased from Nanostructured Carbon (nano-c).\\n\\nFor preparing Cs-oleate solution, CsCO3 (0.407\\u202fg), ODE (20\\u202fmL) and OA (1.25\\u202fmL) were added to a 100\\u202fmL volume of 3-neck round flask, and degassed for 30\\u202fmin\\u202fat 120\\u202f\\u00b0C under vacuum. The flask was filled with N2 gas and degassed again. After repeating this process 3 times, the Cs-oleate solution was prepared and stored in N2. For synthesizing CsPbI3-PQDs, PbI2 (0.5\\u202fg) and ODE (25\\u202fmL) were added to a 100\\u202fmL volume of 3-neck round flask, and degassed for 30\\u202fmin\\u202fat 115\\u202f\\u00b0C. Pre-degassed OA (2.5\\u202fmL) and OLA (2.5\\u202fmL) were injected into the flask, and then the flask was degassed for 30\\u202fmin\\u202fat 115\\u202f\\u00b0C. After the flask was filled with N2 gas, the temperature was raised up to 185\\u202f\\u00b0C and Cs-oleate (2\\u202fmL) was rapidly injected into the flask. After 10\\u202fs, the flask was quenched to room temperature by immersing into ice water. To isolate desired CsPbI3-PQDs, MeOAc (35\\u202fmL) as a polar anti-solvent was added into as-synthesized CsPbI3-PQD solution (15\\u202fmL) and centrifuged at 5000\\u202frpm for 3\\u202fmin. After removing the supernatant, the precipitated CsPbI3-PQDs were dispersed in hexane (5\\u202fmL) and MeOAc (7\\u202fmL) was added. The solution was centrifuged at 5000\\u202frpm for 3\\u202fmin and the supernatant was removed. The precipitated CsPbI3-PQDs was dispersed hexane (15\\u202fmL) and the solution was centrifuged at 5000\\u202frpm for 3\\u202fmin in order to remove the aggregated CsPbI3-PQDs. The precipitates were removed and the supernatant was collected and stored in the dark at 4\\u202f\\u00b0C for 48\\u202fh. After removing the precipitated products, hexane was dried under vacuum and the dried CsPbI3-PQD pellets were dispersed in octane with a concentration of ~75\\u202fmg/mL [,].\\n\\nThe patterned-FTO substrates were cleaned by sonicating sequentially in detergent water, deionized water, acetone and isopropyl alcohol each for 10\\u202fmin. The cleaned FTO substrates were exposed to UV in an UV/O3 instrument in order to eliminate contaminants and make the surface hydrophilic for TiO2 coating. Sol-gel-derived compact TiO2 (c-TiO2) layer used as an electron-transporting layer (ETL) in solar cells was fabricated on the patterned-FTO substrates. The precursor solution was purchased from Sharechem for convenience but the contained chemicals and recipe were same with the reported sol-gel method by Swarnkar et al [,]. The precursor solution was spin-coated onto the FTO substrates at 3000\\u202frpm for 30\\u202fs, and then the substrates were annealed at 500\\u202f\\u00b0C for 1\\u202fh. After cooling to room temperature, the substrates were soaked in TiCl4 aqueous solution (120\\u202fmM) at 70\\u202f\\u00b0C for 1\\u202fh. The substrates were washed with deionized water and annealed at 500\\u202f\\u00b0C for 1\\u202fh. TiCl4 treatment enhances the interfacial quality of the c-TiO2 layer. For the fabrication of CsPbI3-PQD solids based on solid state ligand exchange, CsPbI3-PQD solution in octane (75\\u202fmg/mL) was spin-coated onto the c-TiO2/FTO substrates at 1000\\u202frpm for 20\\u202fs followed by 2000\\u202frpm for 5\\u202fs. The as-cast CsPbI3-PQD film was soaked in the ligand solution (the respective ionic salts in MeOAc) and spin-dried. And then, the ligand-treated film was washed using neat MeOAc and spin-dried. Ligand treatment and washing process were performed under the relatively-controlled humidity condition from 15% to 20% for efficient ligand exchange. This procedure was repeated 4\\u20136 times to build up desired thickness (~300\\u202fnm). Spiro-MeOTAD used as a HTL in solar cells was spin-coated at 4000\\u202frpm for 30\\u202fs. The spiro-MeOTAD solution was prepared as follows: spiro-MeOTAD (72.3\\u202fmg), chlorobenzene (1\\u202fmL), 2-amylpyridine (28.8\\u202f\\u03bcL) and Li-TFSI (17.5\\u202f\\u03bcL) solution in acetonitrile with the concentration of 520\\u202fmg/mL. MoOx and metal electrodes were deposited using a thermal evaporator with a thickness of 15 and 120\\u202fnm, respectively [,]. In case of electron-only devices, we employed PCBM on top of CsPbI3-PQD solids with the device configuration of FTO/c-TiO2/CsPbI3-PQD solids/PCBM/Au. PCBM dissolved in chlorobenzene (20\\u202fmg/mL) was spin-coated at 3000\\u202frpm for 30\\u202fs under a N2-filled glove box.\\n\\nCurrent density\\u2212voltage (J\\u2212V) curves of solar cell devices were carried out under a simulated air mass 1.5 global spectrum (AM 1.5G) and 100\\u202fmW/cm2 illumination (1 sun) using a Newport Oriel Sol3A solar simulator with a xenon lamp and a Keithley 2400 sourcemeter. The J\\u2212V curves of all solar cell devices were measured with an active area of 0.096\\u202fcm2 defined by covering the mask. The J\\u2212V measurement was conducted from forward bias (1.3\\u202fV) to reverse bias (\\u22120.05\\u202fV) at 100\\u202fmW/cm2 and AM1.5\\u202fG. The step size was 13.5\\u202fmV and the delay time was 10\\u202fms. External quantum efficiency (EQE) spectra were measured using a Newport Oriel QuantX300 with an Oriel Cornerstrone 130 monochromator. The EQE spectra were scanned from 300\\u202fnm to 800\\u202fnm with an interval wavelength of 20\\u202fnm. The space-charge-limited-current (SCLC) of electron-only devices was obtained from the J\\u2012V measurements using a Keithley 2400 sourcemeter under dark conditions. Trap-state density (N t) was calculated from trap-filled limit voltage (V TFL), obtained from the SCLC curve, using the equation as follows []: VTFL=qNtL22\\u03b5\\u03b50 where q is the elementary charge, L is the thickness of CsPbI3-PQD solids, \\u03b5 is the relative permittivity of CsPbI3 (\\u03b5\\u202f=\\u202f6.32 \\u03b5 0) and \\u03b5 0 is the vacuum permittivity, respectively. Ultraviolet\\u2013visible (UV\\u2013Vis) absorption spectra were performed using a PerkinElmer Lambda750 UV-vis-near infrared spectrophotometer. Steady-state photoluminescence (PL) measurements were carried out using a Horiba Scientific Flouromax-4 spectrophotometer. Furier-transform infrared (FT-IR) spectra were measured using a Thermo Scientific Nicolet6700. X-ray diffraction (XRD) data was recorded on a Bruker D2 Phaser X-ray diffractometer with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.5406\\u202f\\u00c5). Ultraviolet photoelectron spectroscopy (UPS) and X-ray photoelectron spectroscopy (XPS) were measured using a Thermo Scientific ESCALAB 250Xi analyzer. Atomic force microscopy (AFM) was measured using a Park System NX10 microscope in tapping mode. High-resolution transmission electron microscopy (HR-TEM) images were acquired using a Hitachi HF-3300 with W electron source. Scanning electron microscopy (SEM) images were obtained using a Hitachi SU8230.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: Pb(NO3)2,\\n Perovskite_deposition_solvents: Octane,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: 2-amylpyridine; Li-TFSI,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoOx | Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 528,\\n Stability_PCE_initial_value: 10.7,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.096,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Ni(CH3COO)2\\u00b74H2O powder (99.99%), CH3O(CH2)2OH (99.5%), PbI2 and DMSO are purchased from Sigma-Aldrich Co. Ltd. CH3NH3I (MAI) is purchased from YOUXUAN Technology Co. Ltd. PCBM, \\u03b1-bis-PCBM and Bphen are purchased from Nichem Fine Technology Co. Ltd. GBL is purchased from ACROS ORGANICS Co. Ltd.\\nTo prepare the perovskite precursor solution doped with PCBM or \\u03b1-bis-PCBM, CH3NH3I and PbI2 are dissolved with a molar ratio of 1:1 in GBL and DMSO (v/v, 7:3) mixed solvent, and \\u03b1-bis-PCBM or PCBM is added with the concentration of 6\\u202fmg/mL accordingly, then stir the mixture overnight at 60\\u202f\\u00b0C for 8\\u202fh and filtered through with a 0.45\\u202f\\u03bcm filter before further procedures.\\nNiOx precursor is processed by dissolving 50\\u202fmg Ni(CH3COO)2\\u00b74H2O powder into 1\\u202fmL CH3O(CH2)2OH solution with 12\\u202f\\u03bcL NH2(CH2)2OH as a stabilizing agent to enhance its solubility.\\nThe PSCs based on the structure of FTO/NiOx/active layer/PCBM/Bphen/Ag, shown in Fig. 1 , are fabricated to test the photovoltaic performances of the PSCs, including PCE, photocurrent hysteresis and stability. Three kinds of active layers, MAPbI3, MAPbI3: PCBM and MAPbI3: \\u03b1-bis-PCBM, are used for comparison. The components in active layers are also presented in Fig. 1. NiOx and PCBM are selected as the HTM and ETM respectively for efficient charge extraction in the PSCs. Bphen is applied as an interfacial layer which can flatten the surface of the cathode.\\nThe devices are fabricated on FTO-coated substrate. Firstly, the NiOx is annealing at 400\\u202f\\u00b0C for 60\\u202fmin in air after being coated at 3000\\u202frpm/40\\u202fs on FTO. Then, the MAPbI3 active layer is prepared in the glove box by spin-coating the precursor solution under 4000\\u202frpm/40\\u202fs, followed by stepwise annealing at 100\\u202f\\u00b0C for 10\\u202fmin. After that, PCBM (20\\u202fmg/mL dissolved in chlorobenzene) and Bphen (0.5\\u202fmg/mL dissolved in ethyl alcohol) solution are spin-coated subsequently. Finally, transfer the devices from glove box to an evaporation machine (under 2\\u202f\\u00d7\\u202f10-6\\u202fTorr) to evaporate Ag electrode with an active area of 9.00 mm2. ]\\n\\nSEM images were taken using a Zeiss Supra 55 system at 10\\u202fkV accelerating voltage.\\n\\nAll TAS measurements are carried out in the commercial ultrafast spectroscopy (Helios Fire, Ultrafast Systems, Inc.), an automatic femtosecond transient absorption spectrometer. The femtosecond laser amplifier (Astrella, Coherent, Inc.) delivers 800\\u202fnm laser pulse with pulse duration of ~35 fs. A part of laser energy is guided into the optical parametric amplifier (TOPAS, Coherent, Inc.), which produces the pump pulse with center wavelength of 500\\u202fnm. The rest of the femtosecond laser enters the Helios spectrometer, which implements the scanning of the pump-probe time delay, the supercontinuum white generation and the detection of differential spectra.\\nIn our pump-probe geometry, the pump beam of 500\\u202fnm has the energy fluence of ~0.1\\u202f\\u03bcJ/cm2 on the sample, and the wavelength of the probe beam ranges from 520 to 780\\u202fnm. The pump-probe time delay is scanned from femtosecond to nanosecond time scale. The neat MAPbI3, MAPbI3: PCBM and MAPbI3: \\u03b1-bis-PCBM active layers are coated on quartz plates as samples for TAS scheme.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | Bphen,\\n ETL_additives_compounds: Undoped | Undoped,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: bis-PCBM,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: Undoped,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 200,\\n Stability_PCE_initial_value: 18.22,\\n Stability_PCE_end_of_experiment: 87,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Indium tin oxide (ITO)-coated glass substrates (180\\u202fnm) with a sheet resistance of 8\\u202f\\u03a9/sq were purchased from Huayulianhe Co., Ltd. SnO2 colloid precursor (Sn(IV) oxide, 15% in H2O colloidal dispersion), anhydrous N,N-dimethylformamide (DMF), anhydrous dimethyl sulfoxide (DMSO), anhydrous isopropyl alcohol (IPA) and chlorobenzene were obtained from Alfa Aesar. CH3NH3I (99.5%, denoted as MAI), PbI2 (99.9985%), CH6N3I (denoted as GuaI) and Spiro-OMeTAD were purchased from Xi\\u2019an Polymer Light Technology Co., Ltd. Lithium bis(trifluoromethylsulfonyl) imide (Li-TFSI) and 4-tertbutylpyridine (TBP) were obtained from Aldrich. All of these commercially available materials were used as received without any further purification. The SnO2 colloid precursor was ultrasonically diluted by deionized water (1:5\\u202fvol ratio) for 60\\u202fmin. perovskite precursor solution containing MAI (1.2\\u202fM) and PbI2 (1.2\\u202fM) in anhydrous DMF: DMSO (4:1, v/v) at the ambient temperature, then, filtered with 0.22\\u202f\\u03bcm nylon filter to obtain a clear solution. To obtain the HTM solution, 72.3\\u202fmg of Spiro-OMeTAD was dissolved in 1\\u202fmL of CB with additives of 17.5\\u202f\\u03bcL of LiTFSI solution (520\\u202fmg/mL in ACN) and 28.8\\u202f\\u03bcL of TBP.\\n\\nITO glass substrates were cleaned with alkaline detergent, acetone, absolute ethanol, deionized water for 15\\u202fmin, respectively, and then dried with a nitrogen flow and further cleaned by UV-ozone for 10\\u202fmin before they were used for spin-coating. The acquired SnO2 solution was spin-coated onto the glass/ITO substrate at 3000\\u202frpm for 30\\u202fs and then baked on a hot plate at 150\\u202f\\u00b0C for 30\\u202fmin. After cooling down to room temperature, the perovskite precursor was spin-coated on SnO2 substrate at 3000\\u202frpm for 30\\u202fs, in which 150\\u202f\\u03bcL of CB was dropped on the spinning substrate 12\\u202fs prior to the end of the step. The substrates were then annealed on hotplate at 65\\u202f\\u00b0C for 10\\u202fmin and 100\\u202f\\u00b0C for 30\\u202fmin to obtain MAPbI3 perovskite films. To grow an additional (GuaMA)PbI3 perovskite layer, 100\\u202f\\u03bcL of GuaI solution dissolved in isopropanol with different concentrations were further spin-coated on the as-prepared perovskite substrates at 5000\\u202frpm for 30\\u202fs, and annealed at 100\\u202f\\u00b0C for 10\\u202fmin. Note that GuaI/IPA solution should be added onto the perovskite films very fast, and the solution needs to be kept on the films for 1\\u20133\\u202fs before spin-coating. Subsequently, 70\\u202f\\u03bcL of Spiro-OMeTAD solution was spincoated on the perovskite layers at 4000\\u202frpm for 20\\u202fs. Finally, the devices were completed by depositing 80\\u202fnm of gold electrodes using thermal evaporation.\\n\\nThe field emission scanning electron microscope (FESEM) images were obtained on a ZEISS SUPRA55. X-ray diffraction (XRD) patterns were collected with a SmartLab from Rigaku at 40\\u202fKv and 150\\u202fmA by using Cu-Ka radiation (\\u03bb\\u202f=\\u202f0.15405\\u202fnm). AFM figures were measured using 300HV scanning force microscope (SEIKO). The photovoltaic performance of PSCs was recorded using a Keithley 2400 source meter under one-sun AM 1.5G (100\\u202fmW/cm2) illumination with a solar light simulator (Newport Oriel Sol3A Class AAA, 64023A Simulator), which was calibrated using a NREL standard Si solar cell. EIS measurements were conducted by an electrochemical workstation (CHI660d) (0.1\\u202fMHz\\u2013100\\u202fHz) using the A.C. impedance mode and the fitting software was Zview software. The UV\\u2013vis light absorption measurement was performed by using an ultraviolet\\u2013visible (UV\\u2013vis) spectrophotometer (Shimadzu UV-3101 PC). The external quantum efficiency (EQE) measurements were obtained on a Keithley 2000 multimeter as a function of the wavelength from 350 to 800\\u202fnm on the basis of a Spectral Products DK240 monochromator. The photoelectron spectra were analyzed using a photoelectron spectrometer (AC-2, Riken Keiki). The PL spectra and fluorescence decay curves were taken out with combined steady state (FLS980, Edinburgh). The active area of the cell is 0.1\\u202fcm2. All samples were measured in air (25\\u202f\\u00b0C).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: GuaI,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65; 100,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 30.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 360,\\n Stability_PCE_initial_value: 18.54,\\n Stability_PCE_end_of_experiment: 55,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"ZnO nanoparticles were synthesized by combining the previously reported work with some modifications. In a typical procedure, 52 mL of KOH methanol solution (354 mM) was first added dropwise into a 100 mL of Zn(CH3COO)2\\u00b72H2O methanol solution (107 mM) in a 65 \\u00b0C water bath and continuously stirred for 2.5 h. Then, the products were washed with anhydrous methanol solution for several times to remove residual precursors. Finally, the prepared ZnO nanoparticles were dispersed into a 20 mL mixture solution of n-butanol\\u2013methanol\\u2013chloroform (14:1:1 volume ratio), where the content of ZnO nanoparticles is about 20 mg mL\\u22121. The obtained ZnO solution was filtered by a 0.45 \\u03bcm PTFE syringe filter before spin-coating.\\n\\nFTO rigid glass substrates (1.5 cm \\u00d7 2.0 cm) were etched by zinc power and 2 M HCl, and treated successively with abluent, deionized water, acetone and UV-ozone to achieve a clean surface. After that, the ZnO nanoparticles solution was spin-coated over the FTO substrate at 3000 r.p.m. for 30 s and then dried for 10 min at room temperature. This process was repeated several times to obtain an optimal thickness of ZnO film. Consecutively, the ZnO film was aged 24 h in air at room temperature. Then, solution of PbI2 in N,N-dimethylformamide (DMF) (460 mg mL\\u22121) was spin-coated onto the surface of ZnO films at 3000 r.p.m. for 20 s. After drying the PbI2 layer, the substrate with both ZnO and PbI2 layers was immersed into a solution of CH3NH3I in 2-propanol (10 mg mL\\u22121) for 1 min, followed by thermal annealing at 80 \\u00b0C for 20 min (FTO/ZnO/CH3NH3PbI3). Subsequently, the hole transfer material 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene (Spiro-OMeTAD) was deposited on the top of FTO/ZnO/CH3NH3PbI3 at 4000 r.p.m. for 30 s, where 80 mg of spiro-OMeTAD was dissolved in the mixture solution of 28.5 \\u03bcL 4-tert-butypyridine, 17.5 \\u03bcL lithium bis(trifluoromethane-sulfonyl)imide (Li-TFSI) (520 mg of Li-TFSI in 1 mL of acetonitrile) and 1 mL chlorobenzene. Finally, Ag counter electrode with 100 nm in thickness was deposited via vacuum thermal evaporation. In this work, the solar cells involving the structure of FTO/ZnO/CH3NH3PbI3/Spiro-OMeTAD/Ag were fabricated, measured and stored under ambient conditions without any specific protection, where the humidity and temperature are about 30% and 25 \\u00b0C, respectively.\\n\\nXRD patterns were collected on a Shimadzu X-ray diffractometer 6000 with Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5), which was used to characterize the crystal structure and phase of material. Raman spectra were obtained on a Renishaw in via confocal micro-Raman spectroscopy system. Fourier transform infrared spectra (FT-IR) were recorded on an Avatar 360 (Nicolet) instrument. The morphology of ZnO nanoparticles and film were characterized by a transmission electron microscope (TEM, FEI, Tecnai G2 F20) and a scanning electron microscopy (SEM, Hitachi S4800 HSD).\\nPhotocurrent density\\u2013photovoltage (J\\u2013V) performance of the devices were measured using an electrochemical workstation (VersaSTAT 3, Ametek, USA), where the cells were illuminated by a 150 W xenon lamp class ABB solar simulator (94021A, Newport, USA) under an AM1.5G radiation at a calibrated intensity of 100 mW cm\\u22122, as standardized by a standard Si solar cell (1218, Newport, USA). Incident photon-to-electron conversion efficiency (IPCE) was recorded by a solar cell quantum efficiency measurement system (QTest Station 500D, Crowntech, USA) equipped with a power source (300 W tungsten lamp), a monochromator and a multimeter. The active area of the cell was confirmed to be 0.12 cm2 through a nonreflective metal mask.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 80.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 20.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 840,\\n Stability_PCE_initial_value: 9.19,\\n Stability_PCE_end_of_experiment: 68,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CdSe QDs were obtained from Mesolight Inc. CH3NH3I and PCBM were received from 1-Material. PEDOT:PSS (Clevios PVP AI 4083) aqueous solution was purchased from Heraeus. PbI2, PbCl2, dimethyl sulfoxide (DMSO) and \\u03b3-butyrolactone (GBL) were supplied by Sigma-Aldrich. All chemicals were used as received without further processing. CH3NH3PbI3\\u2212xClx was dissolved in a cosolvent of DMSO and GBL (vol. ratio = 3:7) with Pb2+ and CH3NH3I (molar ratio = 1.4 M:1.3 M). The mixture was stirred at 60 \\u00b0C overnight in a glovebox. To synthesize the CdSe/PCBM composite, three different mass ratios (1%, 5%, and 10%) of CdSe and PCBM powder were dispersed in chlorobenzene.\\n\\nITO was cleaned by sonication using detergent, deionized water, acetone, isopropanol, ultraviolet and ozone (UV-Ozone) treatment for 15 min. A thin layer of PEDOT:PSS was coated on a prepared ITO substrate at 4000 rpm for 1 min by spin coating. The substrate was then heated on a hot plate at 120 \\u00b0C for 20 min in air. We preheated the ITO/PEDOT:PSS substrate and CH3NH3PbI3\\u2212xClx mixed solution at 70 \\u00b0C. Then the perovskite layer was deposited onto ITO/PEDOT:PSS by spin-coating a CH3NH3PbI3\\u2212xClx mixed solution at 1000 rpm for 20 s. After that, the obtained layer was spin-coated at 5500 rpm for 60 s. Soon afterwards, it was quenched by dropping 1000 \\u03bcL of anhydrous toluene at 45 s, followed by annealing at 100 \\u00b0C for 20 min. After cooling to room temperature, a layer of CdSe/PCBM was deposited on top of the perovskite layer by spin coating at 2500 rpm for 40 s. 0.6 mg mL\\u22121 Rhodamine 101 solution in isopropanol was deposited by spin coating at 1500 rpm for 40 s onto the PCBM layer. Finally, 1 nm-thick LiF and 100 nm Ag electrodes were thermally evaporated onto the rhodamine layer under a high vacuum of 7.5 \\u00d7 10\\u22124 Pa.\\n\\nThe surface morphology and roughness were evaluated by SEM and AFM. The crystallinity of the CH3NH3PbI3\\u2212xClx perovskite was characterized by using XRD. UV-vis and PL spectra of CH3NH3PbI3\\u2212xClx films with PCBM and CdSe/PCBM on ITO were measured by using a UV-vis spectrophotometer and a PL spectrophotometer. Current\\u2013voltage characteristics of solar cells were tested by using a Keithley model 2400 source/meter (Keithley Instruments, Inc., OH) under the simulated AM 1.5 G illumination (100 mW cm\\u22122). Each solar cell device has an area of 0.11 cm2 and was measured in air.\\n\\nElectronic structure calculations were performed by using the projector augmented wave formalism of DFT as implemented in the Vienna ab initio simulation package. The energy cutoff was set to 480 eV. For the exchange and correlation functional, we used the generalized gradient approximation (GGA) in the Perdew\\u2013Burke\\u2013Ernzerhof (PBE) format. We note that the Heyd\\u2013Scuseria\\u2013Ernzerhof hybrid functional (HSE06) and inclusive of the spin\\u2013orbit coupling effect, and/or quasiparticle self-consistent GW methods were discussed before. However, by considering the large systems of our models and comparing the results of different functionals, we chose to use the GGA-PBE format. The CH3NH3PbI3 surface was considered with a thickness of 8 atomic layers and the CdSe film with 15 layers, and a vacuum thickness of 15 \\u00c5 was added. During structural optimization, all the atoms and the lattice constant were fully relaxed until the atomic forces are smaller than 0.02 eV \\u00c5\\u22121. A 6 \\u00d7 6 \\u00d7 1 grid for Monkhorst\\u2013Packk-point mesh was used to sample the Brillouin zone. It should be noted that CH3NH3PbI3 has a tetragonal crystal structure with a lattice parameter of a = b = 8.86 \\u00c5 and c = 12.66 \\u00c5 at room temperature, and CdSe has a cubic phase of the sphalerite structure with a = b = c = 6.05 \\u00c5, suggesting a very small lattice mismatch in the (001) direction (\\u223c3.4%).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Rhodamine 101 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 70,\\n Stability_PCE_initial_value: 11.22,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were purchased from Aldrich and used as received, unless otherwise specified. MAI and EAI were synthesized according to previously reported techniques. Ethylamine (2.0 M in MeOH, Aldrich; 5.46 mL) and hydroiodic acid (57% w/w aq. soln, stab with 1.5% hypophosphorous acid, Alfa Aesar; 3.00 mL) were stirred at 0 \\u00b0C under N2 for 2 h. The solvent was evaporated in a rotary evaporator under vacuum. The crude residue was dissolved in MeOH (5 mL) and poured into Et2O (200 mL). The precipitate was collected and dried under vacuum to afford EAI as a white product.\\n\\nPVSK cells were prepared using the following device fabrication procedure. Glass/ITO substrates [Sanyo, Japan (8 \\u03a9 \\u25a1\\u22121)] were sequentially patterned lithographically, cleaned with a detergent, ultrasonicated in acetone and isopropyl alcohol, dried on a hot plate at 140 \\u00b0C for 10 min, and treated with oxygen plasma for 5 min. PEDOT:PSS (Baytron P-VP AI4083) was passed through a 0.45 \\u03bcm filter and deposited onto ITO (thickness: ca. 40 nm) through spin-coating (3000 rpm) in air; the sample was then dried at 140 \\u00b0C for 20 min inside a glove box. The PVSK precursor solution was prepared by dissolving MAI and lead(II) chloride (molar ratio, 3:1) at 25 wt% (with various vol% of EAI) in DMF and then stirring continuously overnight at 60 \\u00b0C in the dark. PVSK devices, having the layered configuration glass/ITO/PEDOT:PSS/MAPbI3\\u2212xClx/PC61BM/Al, were fabricated using methods similar to those reported previously. Prior to deposition of the PVSK layer, the PEDOT:PSS film was preheated at 60 \\u00b0C for 5 min. The precursor solution was also preheated at 60 \\u00b0C for 5 min and then deposited on top of the PEDOT:PSS layer. PCBM was spin-coated (2000 rpm) from a chlorobenzene solution (10 mg mL\\u22121). The layers of Al (100 nm) were deposited thermally under vacuum. The active area of the device was 10 mm2. The cell performance was measured inside a glove box. The current\\u2013voltage (I\\u2013V) properties of the devices were measured using a computer-controlled Keithley 2400 source measurement unit (SMU) and a Newport solar simulator (Oriel\\u00ae Sol2A Class ABA Solar Simulators) under AM 1.5 illumination (100 mW cm\\u22122). The illumination intensity was calibrated using a standard Si reference cell and a KG-5 filter. EQEs were measured using an Enlitech QE-R spectral response measurement system to calibrate the current densities of the devices. UV-vis absorption spectra were recorded using a Hitachi U-3300 spectrophotometer. The morphologies of the perovskite surface were analyzed through AFM using a VEECO DICP-II instrument operated in the tapping mode at ambient temperature; the etched Si probe exhibited a resonant frequency of 131 kHz and a spring constant of 11 N m\\u22121. ImageJ was used to calculate the surface coverages of the films. GIWAXS patterns were collected using a Philips Panalytical-x'PertPROMRD instrument; the incident beam angle was above the critical angle (ca. 0.5\\u00b0). Cross-sectional SEM images were measured using a JEOL JSM 6701F field-emission scanning electron microscope.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 65.0; 65.0,\\n Stability_atmosphere: Ar,\\n Stability_time_total_exposure: 580,\\n Stability_PCE_initial_value: 9.4,\\n Stability_PCE_end_of_experiment: 30,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"P3HT had a regioregularity of greater than 95% and a number-average molecular weight range of 25000\\u201335000 g mol\\u22121 (polydispersity <2) and was used as received (Aldrich). Spiro (N2,N2,N2\\u2032,N2\\u2032,N7,N7,N7\\u2032,N7\\u2032-octakis(4-methoxyphenyl)-9,9\\u2032-spirobi[9H-fluorene]-2,2\\u2032,7,7\\u2032-tetramine, Fenglin Chemicals, 99.5%) was also used as received. PTAA was purchased from Aldrich and had a number-average molecular weight of 7000\\u201310000 g mol\\u22121 with a polydispersity of 2.0\\u20132.2 and used as received. Styrene (\\u226599%), divinylbenzene (DVB, 80%) 4,4\\u2032-azobis(4-cyanovaleric acid) (ACVA, 98%), toluene (99.8%), chlorobenzene (CBZ, 99.8%), isopropanol (IPA, anhydrous, 99.5%), 4-tert-butylpyridine (TBP, 96%), lithium bistrifluoromethanesulfonimidate (LiTFSI, 99.95%) were all purchased from Sigma-Aldrich and used as received. Methyl amine solution (33 wt% in absolute ethanol) and hydriodic acid (57 wt%), titanium diisopropoxide bis(acetylacetonate) (TDB, 75 wt% in IPA) and PbCl2 (98%), anhydrous N,N-dimethylformamide (DMF, 99.8%) were also purchased from Aldrich and used as received. Methylammonium iodide was synthesised and purified using the method previously reported. Titania paste (TiO2, 18 NRT) was purchased from Dyesol and used as received. Water was of ultrahigh purity and de-ionised.\\n\\nPS MG was prepared using surfactant-free emulsion polymerisation following the method reported earlier. Briefly, water (265 ml) was adjusted to pH of 9.0 using NaOH solution and then added to a 500 ml reaction vessel and stirred at 200 rpm at 70 \\u00b0C and deoxygenated. ACVA (0.244 g, 0.871 mmol) was dissolved in water (7.0 ml) and adjusted to pH of 11.0 using aqueous NaOH solution. DVB (0.086 g, 0.661 mmol) was mixed with styrene (28.6 g, 0.275 mol) and added to the vessel. The ACVA solution was then quickly added under a N2 atmosphere and the mixture stirred for 16 h. The particle dispersion (in collapsed, latex, form) was purified using repeated centrifugation and re-dispersion in water. After purification, the dispersion was freeze-dried and the powder re-dispersed in toluene or CBZ. To aid re-dispersion a few drops of methanol were added prior to solvent addition. The MG had a nominal composition of 99.7 wt% styrene and 0.3 wt% DVB.\\n\\nAll solution and film preparation steps (including annealing) were conducted in a glove box (humidity \\u223c2%). Laser-patterned, ITO-coated glass substrates (20 \\u03a9 sq\\u22121) were cleaned by ultrasonication in a 2% Hellmanex solution, rinsed with water and IPA, and dried. A TiO2 hole-blocking layer (bl-TiO2) (48 nm) was spin-coated at 2000 rpm for 60 s onto the ITO using TDP solution in 1-butanol (0.15 M) and subsequent heating at 125 \\u00b0C for 5 min. The procedure was repeated using TDB solution (0.30 M). Titania paste (70 \\u03bcL, 1:5 in ethanol) was spin-coated onto the cleaned glass slides at 5000 rpm for 30 s to form a mesoporous scaffold (mp-TiO2). The films were then annealed at 500 \\u00b0C for 30 min and had an average thickness of 250 nm. After cooling to room temperature a MAPI(C) precursor solution was spin-coated onto ITO/bl-TiO2/mp-TiO2 substrate at 2000 rpm for 60 s. The precursor solution contained MAI and PbCl2 (3:1 molar ratio) in DMF (30 wt%). The film was dried at 100 \\u00b0C for 45 min. The capping layer thickness was \\u223c250 nm. All films were stored in a desiccator over P2O5 in the dark until investigation.\\n\\nAll stages of device preparation were conducted in the glove box. The procedure to form the ITO/bl-TiO2/mp-TiO2/MAPI(C) films was described above. PTAA solution was prepared by adding PTAA (15 mg) to CBZ (0.865 g) at room temperature. LiTFSI (15 \\u03bcl, 170 mg ml\\u22121) and t-BP (7.5 \\u03bcl) were also added. The PTAA solution was spin-coated onto the MAPI(C) layer at 4000 rpm for 30 s to give an average PTAA thickness of 120 nm. PTAA-MG composite HTMs were prepared using mixed dispersions containing MG particles and PTAA. The MG dispersion was prepared using MG (64 mg) in CBZ at room temperature with a total dispersion weight of 1.0 g. PTAA solution (3.0 wt%) was prepared by adding PTAA (30 mg) to CBZ (total weight 1.0 g) at room temperature. The MG dispersion and PTAA solution were then mixed at a weight ratio 0.47:0.53. LiTFSI (15 \\u03bcl, 170 mg ml\\u22121) and t-BP (7.5 \\u03bcl) were added. The PTAA-MG films were formed by spin-coating at 4000 rpm for 30 s and had an average thickness of 180 nm.\\nSimilar procedures to those described above were used for the devices containing P3HT and P3HT-MG. The solvent used in these cases was toluene at 70 \\u00b0C. For the P3HT systems, LiTFSI (10 \\u03bcL) and TBP (10 \\u03bcL) were added. The average film thicknesses for the P3HT and P3HT-MG HTMs were 100 nm and 160 nm, respectively. For the Spiro-containing films, CBZ was used as the solvent at room temperature; LiTFSI (4.8 \\u03bcl, 520 mg ml\\u22121) and TBP (8.0 \\u03bcl) were also added. The average thicknesses for the Spiro and Spiro-MG films were 450 nm and 160 nm, respectively.\\nFor all devices, a gold layer (80 nm) was deposited by thermal evaporation onto the HTMs and HTM-MG composite layers. In the case of MG encapsulation the MG particles were dispersed in toluene at a concentration (CMG) of 3.0 wt%. The MG dispersions were spin-coated at 3000 rpm for 30 s at room temperature. The thickness of the encapsulating MG layer was 145 nm.\\n\\nDynamic light scattering (DLS) measurements were conducted using a 50 mW He/Ne laser operated at 633 nm with a standard avalanche photodiode (APD) and 90\\u00b0 detection optics connected to a Malvern Zetasizer Nano ZS100 autocorrelator. XRD patterns were obtained using a Bruker D8 Advance diffractometer (Cu-K\\u03b1). Films were scanned between 10 and 50\\u00b0 with a step size of 0.05. The films were prepared and measured under a nitrogen atmosphere. Atomic force microscopy (AFM) images were obtained using an Asylum Research MFP-3D operating in AC (\\u201ctapping\\u201d) mode. UV-visible spectra were obtained using a Hitachi U-1800 spectrophotometer. Film thickness measurements were conducted using a Dektak 8 Stylus Profilometer (Bruker). Contact angle measurements were performed using water and a Kr\\u00fcss Drop Shape Analysis (DSA100). Photoluminescence (PL) spectra were obtained using an Edinburgh Instruments FLS1080 spectrometer. The beam was incident on the film surface side and an excitation wavelength of 480 nm was used. The substrates were ITO/bl-TiO2/mp-TiO2 for the films containing MAPI(C) or glass for the samples that did not contain MAPI(C).\\n\\nThe current density\\u2013voltage (J\\u2013V) curves were measured using a Keithley 2420 sourcemeter, 100 mW cm\\u22122 illumination (AM 1.5G) and a calibrated Oriel Si-reference cell that had been certified by NREL. An Oriel solar simulator (SOL3A) was used for these measurements. The active area of the devices (0.025 cm2) was defined using a square aperture within a mask. The data shown are from the reverse scan unless otherwise stated (Voc to Jsc) and the sweep rate was 100 mV s\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 20.0; 20.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 24,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.025,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Formamidinium iodide (FAI) and methylammonium bromide (MABr) were purchased from Dyesol. Lead iodide (PbI2) and lead bromide (PbBr2) were obtained from TCI. Cesium iodide (CsI) was purchased from GmbH. Phenylethylammonium iodide (PEAI) was synthesized. 10 ml of phenylethylamine was diluted in 20 ml of anhydrous ethanol and cooled in an ice bath. With vigorous stirring, 20 ml of HI (55 wt% in H2O, Sigma Aldrich) was slowly added dropwise. After stirring for 20 min, a colorless precipitate was filtered. The precipitate was washed with diethyl ether and dissolved in methanol twice. To obtain pure white crystals, the PEAI precipitate was recrystallized twice and stored in a vacuum oven overnight to dry.\\n\\nFTO glass substrates (Nippon sheet glass) were sequentially cleaned with detergent solution, acetone, and ethanol. And then by spray pyrolysis deposition, a compact TiO2 layer was coated on the cleaned FTO substrate heated at 450 \\u00b0C. The precursor solution was prepared by diluting titanium diisopropoxide (Sigma-Aldrich) in ethanol (0.6 ml:10 ml). After cooling, a mesoporous TiO2 film was prepared by coating a diluted TiO2 paste (Dyesol 30 NR-D) solution in ethanol. Right after spin-coating at 2000 rpm for 20 s, the substrates were sintered on a hot plate at 500 \\u00b0C for 30 min. For doping Li on TiO2, the films were treated with 0.1 M lithium bistrifluoromethanesulfonimidate solution (Li-TFSI, Aldrich) in acetonitrile by spin-coating at 3000 rpm for 10 s, and were finally baked at 500 \\u00b0C for 30 min again. The lead excess (FAPbI3)0.85(MAPbBr3)0.15 precursor solution was prepared by mixing FAI (1.1 M), PbI2 (1.15 M), MABr (0.2 M) and PbBr2 (0.2 M) in a mixed solvent of DMF:DMSO = 4:1 (volume ratio). Another 1.15 M solution of CsPbI3 was also prepared in DMF:DMSO (with the same volume ratio). For triple cation mixed perovskite solution, (FAPbI3)0.85(MAPbBr3)0.15 and CsPbI3 solutions were mixed in 10 vol% ratio. The solution was then spin-coated at 1000 rpm for 10 s and continuously at 4000 rpm for 30 s in a nitrogen glove box. After entering the second step, 100 \\u03bcl of anhydrous trifluorotoluene was poured 15 seconds before the completion of the process. Films were then annealed at 100 \\u00b0C for 60 min. For forming an additional 2D perovskite film on top of this perovskite film, cooled substrates were treated with a PEAI isopropanol solution. 100 \\u03bcl of PEAI solution (15 mg ml\\u22121) were spin-coated on the as-prepared perovskite films at 4000 rpm, which is similar to the anti-solvent dropping method. Finally, spiro-OMeTAD was spin-coated at 4000 rpm for 20 s. A 70 mM spiro-OMeTAD solution was prepared by dissolving in chlorobenzene with 4-tert-butylpyridine, Li-TFSI in acetonitrile, and Co[t-BuPyPz]3[TFSI]3 (FK209) in acetonitrile at a molar ratio of spiro:FK209:Li-TFSI:TBP of 1:0.03:0.5:3.3. Devices were completed with thermal evaporation of a 70 nm thick gold counter electrode.\\nFor devices based on the planar SnO2 ETL, compact TiO2/FTO substrates were prepared as explained previously for mesoporous TiO2. A PTO layer was prepared by spin-coating a precursor solution of SnCl4 (Acros) dissolved in water. 0.1 M SnCl4 aqueous solution was spin-coated at 5000 rpm for 10 s on the substrates to get \\u223c20 nm thickness. Then the substrates were transferred onto a hotplate and heated at 180 \\u00b0C for 1 h and cooled down.\\n\\nX-ray diffraction (XRD) analysis in an angle range of 2\\u03b8 = 3\\u00b0 to 30\\u00b0 was carried out using a Bruker D8 Advance diffractometer. The absorbance and reflectance measurements were performed with an integrating sphere using a UV/Vis/NIR spectrophotometer (PerkinElmer Lamda). Photoluminescence were measured using a Flourolog-3 (Horiba Scientific) with an excitation laser of 450 nm. High-resolution scanning electron microscope (SEM) images were obtained on a ZEISS Merlin at an accelerating voltage of 5 kV. Atomic force microscopy (AFM) images were acquired using a Park NX10 (Park system) and analyzed with XEI AFM data analysis software.\\nTime-resolved PL experiments were performed with a spectrophotometer (Gilden Photonics) using a pulsed source at 480 nm (Ps diode lasers BDS-SM). The time-resolved signals were recorded by a Time Correlated Single Photon Counting detection technique with a time resolution of 1 ns.\\nFor the STEM and STEM-EDX measurements, cross-sectional lamellae were prepared from the devices using the conventional focused ion beam (FIB) lift-out technique on a Zeiss Nvision 40. To reduce FIB induced damage, a final thinning in the FIB at 5 kV using a beam current of 80 pA was employed. To minimize exposure to air, the data were acquired just after the FIB preparation. STEM imaging and energy dispersive X-ray analysis were performed on an aberration-corrected FEI Titan Themis 60-300 transmission electron microscope in scanning mode at an accelerating voltage of 200 kV. This microscope is equipped with a high brightness X-FEG gun and Bruker Super-X EDX detectors (four windowless silicon drift detectors).\\nThe impedance spectra measurements were carried out with an SP-200 BioLogic potentiostat with an AC perturbation of 10 mV from 75 mHz to 1 MHz, at room temperature with 5% humidity. The illumination was tuned with an Oriel DC Regulated illuminator in order to make Voc = 880, which corresponds to the operation region of the samples (Voc = 1.1 V at 1 sun). With fitting purposes, in addition to the elements included in the equivalent circuit shown in the inset of Fig. 4A, extra series resistive and inductive elements were also considered. In the equivalent circuit Rb and Cb are the resistive and capacitive elements, respectively, behind the high frequency arc in the Nyquist plot, whose physical meaning is related to dielectric and chemical bulk properties. On the other hand, RS and CS analogously characterize the high frequency arc whose nature may be associated with interface phenomena.\\nUltra-violet photoelectron spectroscopy (UPS) was carried out in an ultrahigh vacuum. The photon line width was \\u223c250 meV and the minimum spot size was \\u223c1 mm. He I photons (21.2 eV) with a bias of 5 eV were used to acquire the spectra at a normal emission level. The photoelectrons were collected using a Sigma Probe (Thermo VG Scientific) with 50 meV precision.\\n\\nPhotovoltaic performance was evaluated using commercial solar simulators (Oriel, 450 W, Xenon, AAA class). The light intensity was matched to one sun (AM 1.5G or 100 mW cm\\u22122) by calibrating with a Si reference cell equipped with an IR-cutoff filter (KG5, Newport), and it was done before each measurement. Current\\u2013voltage (J\\u2013V) curves of the PSCs were obtained by applying an external voltage bias while measuring the current response using a Keithley 2400 digital source meter. The voltage scan rate was 25 mV s\\u22121 in forward and reverse scans. Devices were not preconditioned such as light soaking or a pre-voltage bias applied before starting the measurement. The cells were masked with an active area of 0.16 cm2. EQE was measured using an IQE200B (Oriel) without bias light.\\nStability tests were carried out in a sealed cell holder with a glass cover (house made), where argon gas was filled to remove the residual water and oxygen from the holder. For the ambient condition test, the argon gas was turned off and the humidity and oxygen were not controlled, and the cells were encapsulated with surlyn (solaronix) and glass coverslips. In this case, the humidity was not controlled but the laboratory humidity was monitored, which ranged from 30 to 60% relative humidity at room temperature. In the glass cover, 0.1225 cm2 masks were equipped. The LED lamp used in the system had a light intensity of 100 mW cm\\u22122. J\\u2013V curves were recorded on an electronic system using a 22 bit delta-sigma analog to digital converter. A scan rate of 25 mV s\\u22121 with a step size of 5 mV was used and the devices were kept at the temperature of 50 \\u00b0C. Every 2 hours the J\\u2013V measurement and maximum power point tracking were performed. A reference Si-photodiode was placed in the same holder to check the intensity of the light.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | Li-TSFI,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: Cs0.1FA0.76MA0.14PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 50.0; 50.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 800,\\n Stability_PCE_initial_value: 20,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO glass (Nippon sheet glass) substrates were sequentially cleaned with the detergent solution, acetone, and ethanol. A compact TiO2 layer was then coated on the cleaned FTO substrate by spray pyrolysis deposition at 450 \\u00b0C with a precursor solution prepared by diluting titanium diisopropoxide (Sigma-Aldrich) in ethanol. Mesoporous TiO2 films were prepared using a diluted TiO2 paste (Dyesol 30 NR-D) in ethanol solution. Films were spin-coated at 2000 rpm for 20 s, and sintered on a hot plate at 500 \\u00b0C for 30 min. After cooling to room temperature, films were treated with 0.1 M Lithium bistrifluoromethanesulfonimidate solution (Li-TFSI, Aldrich) in acetonitrile by spin-coating at 3000 rpm for 10 s, and finally baked again at 500 \\u00b0C for 30 min. The lead excess (FAPbI3)0.85(MAPbBr3)0.15 precursor solution was prepared by mixing FAI (1.1 M), PbI2 (1.15 M), MABr (0.2 M) and PbBr2 (0.2 M) in a mixed solvent of DMF:DMSO = 4:1 (volume ratio). The solution was then spin-coated at 1000 rpm for 10 s and continuously at 6000 rpm for 30 s. During the second step, 100 \\u03bcL of anhydrous chlorobenzene was poured 15 seconds before the process was finished. Films were then annealed at 100 \\u00b0C for 90 min. For the surface passivation treatment, the films were cooled down to room temperature and treated with a FABr solution. 100 \\u03bcL of FABr solution (5 mg ml\\u22121) were spin-coated on the as-prepared perovskite substrates at 5000 rpm for 30 s, and annealed at 100 \\u00b0C for 5 min. Finally, Spiro-OMeTAD was spin-coated at 4000 rpm for 20 s. The Spiro-OMeTAD solution was prepared by dissolving in chlorobenzene at 70 mM and adding 4-tert-butylpyridine, Li-TFSI in acetonitrile, and Co[t-BuPyPz]3[TFSI]3 (FK209) in acetonitrile at the molar ratio of Spiro:FK209:Li-TFSI:TBP of 1:0.03:0.5:3.3. Devices were fabricated with a 70 nm thick gold counter electrode by using thermal evaporation.\\n\\nX-ray diffraction (XRD) analysis was carried out using a Bruker D8 Advance diffractometer in an angle range of 2\\u03b8 = 10\\u00b0 to 30\\u00b0. The morphology of the films was characterized using a high-resolution scanning electron microscope (SEM, ZEISS Merlin). The energy dispersive X-ray (EDX) spectra and composition analysis were performed with SEM. It was carried out two days after preparing the films. The absorbance and reflectance were measured with an integrating sphere using UV/Vis/NIR spectroscopy (PerkinElmer Lambda). The photoluminescence dynamics were measured using the Time-Resolved Single Photon Counting (TRSPC) technique that is incorporated into the same Fluorolog-312 spectrofluorometer. The solar cell measurement was done using commercial solar simulators (Oriel, 450 W Xenon, AAA class/Oriel VeraSol-2, LED, AAA class). The light intensity was calibrated with a Si reference cell equipped with an IR-cutoff filter (KG5, Newport), and it was recorded before each measurement. Current\\u2013voltage characteristics of the cells were obtained by applying an external voltage bias while measuring the current response using a digital source meter (Keithley 2400/2604). The voltage scan rate was 10 or 25 mV s\\u22121 and no device preconditioning such as light soaking, or forward voltage bias applied for a long time, was applied before starting the measurement. The cells were masked with an active area of 0.16 cm2 to fix the active area and reduce the influence of the scattered light. EQE was measured with IQE200B (Oriel) without bias light.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | Li-TFSI,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 90,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 400,\\n Stability_PCE_initial_value: 19.1,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Graphene oxide was prepared by oxidation of natural graphite powder according to a modified Hummers' method. Briefly, graphite powder (1.0 g) was sonicated in concentrated sulfuric acid (30 mL, 96\\u201398%) at 23 \\u00b0C for 1 h. NaNO3 (0.5 g) was added under stirring ; the mixture was cooled in an ice bath. Under vigorous stirring, KMnO4 (6.0 g) was added slowly. The reaction system was transferred to an oil bath (37\\u201340 \\u00b0C) for about 1 h. H2O (200 mL) was added slowly, with stirring for another 30 min while the temperature was increased to 70\\u201380 \\u00b0C. In the final step, H2O (200 mL) was added, followed by a slow addition of H2O2 (5\\u20137 mL, 30%); in this stage, the colour of the solution changed from brown to yellow. The mixture was centrifuged and washed with HCl aqueous solution (5%), followed by repeated washing with H2O and then with DMF. The resulting solid was dispersed in DMF with agitation followed by ultra-sonication. The obtained brown dispersion was centrifuged (30 min, 3000 rpm) to remove unreacted graphite or agglomerated sheets.\\n\\nThe synthesized CH3NH3I powder was mixed with PbI2 (Alfa Aesar) in a 1:1 molar ratio in anhydrous DMF at 70 \\u00b0C for 3 h with a CH3NH3PbI3 (PSK) concentration of 45 mass%. Graphene oxide was dispersed in DMF (concentration 0.5 mg mL\\u22121). A blended solution was prepared on mixing the stock solution of perovskite and graphene oxide solution. The concentration of perovskite in both pristine PSK solution and PSK:GO solution was fixed to 45 mass%; PSK:GO solutions were prepared with graphene oxide (GO) at mass concentrations of 0.025, 0.05 and 0.075 mg mL\\u22121. After the pre-cleaned ITO substrates were treated with UV\\u2013ozone for 18 min the GO layer was spin-coated on the ITO substrates at 4000 rpm (torsion rate: 12000 rpm s\\u22121) with the GO solution of 0.5 mg mL\\u22121 concentration, followed by annealing at 125 \\u00b0C for 10 min. The perovskite films were deposited using the solvent-induced method. Pristine PSK solution or PSK:GO solution was first spin-coated on top of the ITO/GO substrate at 5000 rpm (torsion rate: 10000 rpm s\\u22121). With a delay period of 5 s, chlorobenzene was dropped on the substrate to promote rapid nucleation, followed by annealing at 100 \\u00b0C for 2 min. The films were subjected to solvent annealing: the perovskite film was kept under DMF vapor at 100 \\u00b0C for 10 min. PCBM solution in chlorobenzene (2 mass%) was spin-coated on a pristine PSK layer or a PSK:GO hybrid composite layer at 1000 rpm (torsion rate: 1000 rpm s\\u22121) for 30 s to serve as an electron-transport layer. Ag (100 nm) was deposited by thermal evaporation in a vacuum system (pressure 5 \\u00d7 10\\u22126 Torr); with a metal mask the active area of the device was 0.0225 cm2.\\n\\nA field-emission scanning electron microscope (FESEM, Hitachi SU8010) and atomic force microscope (VT SPM, SII Nanotechnology Inc.) were used to investigate the morphology and structure of the samples. The X-ray diffraction (XRD) patterns of the thin films coated on the ITO substrates were obtained with an X-ray diffractometer (Bruker AXS, D8 Advance, Cu K\\u03b1 irradiation, \\u03bb = 154.18 pm). The Raman spectra of graphene oxide confirmed two lines at G (1605 cm\\u22121) and D (1339 cm\\u22121). The functional groups of various types were deduced from the infrared (FTIR) spectra of GO. The current density\\u2013voltage characteristics of the devices were recorded with a digital source meter (Keithley 2400) under one-sun illumination (AM 1.5G, 100 mW cm\\u22122) with a solar simulator (XES-40S1, SAN-E1), calibrated with a silicon diode and a KG-5 filter to decrease the mismatch of the spectrum. The spectra of incident photons to current (IPCE) were recorded with a system comprising a Xe lamp (A-1010, PTi, 150 W) and a monochromator (PTi). The absorption spectra of the thin-film and solution samples were recorded with a spectrophotometer (JASCO V-570).\\nThe photoluminescence (PL) spectra were recorded in the range of 650\\u2013900 nm with excitation at 635 nm (LDH-635, PicoQuant). The PL transients were recorded with a time-correlated single-photon counting (TCSPC) system (Fluotime 200, PicoQuant, excitation at 635 nm) from a picosecond pulsed-diode laser (LDH-635, PicoQuant, FWHM \\u223c 70 ps). The repetition rate of the laser used for all experiments was 0.5 MHz and the pulse energy was 1 nJ cm\\u22122; the beam size was expanded to 1.5 mm \\u00d7 3.5 mm. The PL temporal profiles were collected at 770 nm, which is the maximum for all the perovskite samples under investigation. The electrochemical impedance spectra (EIS) of all the devices were measured with an electrochemical workstation (IM 6, Zahner, Germany) over the frequency range of 100 mHz to 4 MHz with an ac amplitude of 10 mV under one-sun illumination and open-circuit conditions. The obtained EIS data were fitted (Z-view software) based on the equivalent circuit model. The mobilities and concentrations of the charge carriers of the perovskite films were measured with Hall effect equipment (Nanometrics HL5500 Hall system) performed with four-square gold contacts at the corners. The perovskite films were measured under a magnetic field of 0.5 T and a constant DC current.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Graphene oxide,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Graphene oxide,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 2000,\\n Stability_PCE_initial_value: 15.15,\\n Stability_PCE_end_of_experiment: 75,\\n Cell_area_measured: 0.0225,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Zn(CH3COO)2\\u00b72H2O and all anhydrous solvent were purchased from Aladdin. Lead iodide (PbI2), 4-tert-butypyridine and lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) were purchased from Kanto. Methylammonium iodide (CH3NH3I) and 2, 2\\u2032, 7, 7\\u2032-tetrakis-(N, N-di-4-methoxyphenylamino)-9, 9\\u2032 spirobifluorene (Spiro-OMeTAD) and KOH were obtained from Youxuan Trade, Toronto and Tianjin Fengchuan Chemical Reagent Technologies Co., Ltd, respectively.\\n\\nThe synthesis of ZnO nanoparticles (NPs) is similar to our previous work [37]. In a typical procedure, 2.36\\u202fg Zn(CH3COO)2\\u00b72H2O was first dissolved in 100\\u202fmL of methanol solution. Then, 52\\u202fmL of KOH methanol solution (354\\u202fmM) was added dropwise into the aforementioned solution. Subsequently, the mixture was kept at 65\\u202f\\u00b0C for 2.5\\u202fh under magnetic stirring, leading to the production of ZnO NPs. Then, the obtained ZnO NPs were washed with anhydrous methanol for three times to remove residual precursors. Finally, the ZnO NPs were dispersed into a solution of n-butanol-chloroform-methanol (14:1:1 volume ratio) to form a 20\\u202fmg/mL ZnO solution.\\n\\nAll ZnO-based PSC devices were fabricated on FTO glass substrates (1.5\\u202fcm\\u202f\\u00d7\\u202f2.0\\u202fcm). FTO substrates were first etched by zinc powder and 6\\u202fM HCl, and ultrasonically cleaned successively with detergent, deionized water, acetone, 2-propanol, ethanol, followed by an UV-ozone treatment for 15\\u202fmin. After that, the electron transport material was deposited onto the substrate by spin-coating ZnO solution at 3000\\u202frpm. for 30\\u202fs and dried at 30\\u202f\\u00b0C for 10\\u202fmin. This process was repeated four times to obtain a compact ZnO film. Then, the ZnO film was aged 24\\u202fh under ambient conditions. Subsequently, a two-step spin-coating fabrication protocol was adopted to obtain a high quality perovskite. The PbI2 N, N-dimethylformamide (DMF) solution (460\\u202fmg /mL) was first spin-coated on the FTO/ZnO film at 3000\\u202frpm. for 30\\u202fs and annealed at 70\\u202f\\u00b0C for 10\\u202fmin. Then, a solution of CH3NH3I in 2-propanol (50\\u202fmg/mL) was spin-coated on the surface of PbI2 film at 1000\\u202frpm. for 5\\u202fs and 4000\\u202frpm. for 15\\u202fs and annealed at 80\\u202f\\u00b0C for 30\\u202fmin to form a highly crystalline and compact CH3NH3PbI3 (MAPbI3) layer. For the sake of brevity, as-prepared perovskite was named as spin-coated MAPbI3. As a control experiment, the above mentioned FTO/ZnO/PbI2 film was immersed into a solution of CH3NH3I in 2-propanol (10\\u202fmg/mL) for 40\\u202fs and annealed at 80\\u202f\\u00b0C for 30\\u202fmin to prepare another kind of perovskite layer which was called as immersed MAPbI3 for clarity. After the FTO/ZnO/MAPbI3 films were cooled down to room temperature, the Spiro-OMeTAD hole transfer layer (80\\u202fmg of Spiro-OMeTAD, 28.5 \\u03bcL 4-tert-butypyridine, 17.5 \\u03bcL Li-TFSI (520\\u202fmg of Li-TFSI in 1\\u202fmL of acetonitrile) all dissolved in 1\\u202fmL chlorobenzene) was deposited on the top of FTO/ZnO/MAPbI3 film by spin-coating at 4000\\u202frpm. for 30\\u202fs. Finally, about 60\\u202fnm thick Au counter electrode was deposited on top of perovskite film via vacuum thermal evaporation at an evaporation rate 1.0\\u202f\\u00c5/s. The active area of PSCs was confirmed to be 0.15\\u202fcm2 by a non-reflective metal mask. All processes including fabrication, measurement and storage of devices with the structure of FTO/ZnO/MAPbI3/Spiro-OMeTAD/Au were carried out under ambient conditions (25\\u202f\\u00b0C, 50% relative humidity).\\n\\nX-ray diffraction (XRD) pattern was used to analyze crystal structure, which was recorded on a Panalytical Empyrean X-ray diffractometer with a Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.540598\\u202f\\u00c5) at a scan rate of 10\\u00b0/min. The chemical components of ZnO films with and without aging process were investigated by a Fourier transform infrared spectra (FT-IR, Nicolet, Avatar 360) and an X-ray photoelectron spectroscopy (XPS, Perkin-Elmer, PHI 5400 ESCA system), where the XPS analysis adopted an Al K\\u03b1 radiation source at the Retarding model, and all binding energy values were calibrated using the reference peak of C 1s at 284.6\\u202feV. The morphologies of nanoparticles and films were analyzed by a New Generation Cold Field Emission scanning electron microscopy (SEM, Hitachi, SU8000), a transmission electron microscope (TEM, JEOL, JEM-2100) and an atomic force scanning probe microscope (AFM, Bruber, Dimension Icon). Steady-state photoluminescence (PL) and time-resolved photoluminescence (TRPL) spectra were performed on FLS980 fluorescence spectrometer from Edinburgh Instruments, and the excited wavelength was 500\\u202fnm. Ultraviolet-visible (UV\\u2013vis) absorption spectroscopy measurements were conducted on TU1901 spectrometer (Beijing Purkinje General Instrument Co., Ltd). Static water contact angle was measured using a contact angle instrument (JC2000C1).\\nPhotocurrent density-photovoltage (J-V) curves of PSCs were measured by a binding unit of electrochemical workstation (VersaSTAT 3, Ametek, USA) and a class ABB solar simulator (model 94021A, Newport, USA), where the cells were illuminated using an AM 1.5G sunlight (100\\u202fmW\\u202fcm\\u22122) generating from 150\\u202fW xenon lamp optical source, and the intensity of light was standardized by a Newport Oriel standard PV reference cell system (model 91,150\\u202fV). The scan rate was 0.2\\u202fV/s. Electrochemical impedance spectra (EIS) were performed using a VersaSTAT 3 electrochemical workstation (Ametek, USA) at a frequency ranging from 106 to 0.1\\u202fHz with 5\\u202fmV amplitude in the dark condition. The EIS data was fitted by the software of ZView2 according to the equivalent circuit model. Incident photon-to-electron conversion efficiency (IPCE) was recorded by a QTest Station 500D solar cell quantum efficiency measurement system (CROWNTECH, USA) equipped with a 300\\u202fW tungsten lamp power source, a QEM11-S 1/8 m monochromator, a Keithley 2000 multimeter and an opaque chamber.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 80.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 30.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1080,\\n Stability_PCE_initial_value: 14.25,\\n Stability_PCE_end_of_experiment: 86.25,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The indium tin oxide (ITO) coated glass substrates were ultrasonically cleaned with deionized water, acetone, and isopropanol for 20\\u202fmin in each solvent. Before depositing PTAA (8\\u202fmg/mL, Sigma) hole transport layer (HTL), the ITO substrates were dried with a nitrogen gun and treated with ultraviolet-ozone for 20\\u202fmin. The ITO substrates were then transferred to the nitrogen-filled glovebox. Then PTAA solution dissolved in chlorobenzene with F4-TCNQ (1\\u202fwt %) doping was spin-coated on the ITO substrates at 4,000\\u202frpm for 30\\u202fs and the substrates were annealed at 120\\u202f\\u00b0C for 10\\u202fmin. FA0.8Cs0.2Pb(I0.7Br0.3)3 perovskite precursor solution was prepared according to our previous report. FAI (0.864\\u202fmmol, Dyesol), PbI2 (0.594\\u202fmmol, TCI), PbB2 (0.486\\u202fmmol, TCI) and CsI (0.216\\u202fmmol, Alfa Aesar) were dissolved in 1\\u202fmL mixed solvent of DMSO and DMF with a volume ratio of 3:1. Additional Pb(SCN)2 (Sigma-Aldrich) with the different molar ratio to PbI2 (from 0% to 2%) was added into the perovskite precursor solution. All the solutions were stirred at 60\\u202f\\u00b0C overnight before use. To improve the wettability of PTAA HTL, 70\\u202f\\u03bcL DMF was spin-coated at 4000\\u202frpm for 10\\u202fs without annealing. 100\\u202f\\u03bcL of the perovskite precursor solution was dropped on the pre-wetted substrate and then spin-coated on PTAA HTL at 500\\u202frpm for 2\\u202fs and at 4,000\\u202frpm for 60\\u202fs with 750\\u202f\\u03bcL diethyl ether dripping at the 25\\u202fs of the second step. Then the as-prepared films were annealed at 65\\u202f\\u00b0C for 2\\u202fmin and 100\\u202f\\u00b0C for 10\\u202fmin. For the devices with solvent annealing, the substrates were covered by a petri dish including 10\\u202f\\u03bcL DMF throughout the same annealing process from 65 to 100\\u202f\\u00b0C. For the samples with GABr treatment, a GABr (TCI) in isopropanol solution was directly dropped on the static perovskite films and spin-coated at 4000\\u202frpm for 30\\u202fs. The samples were then annealed at 105\\u202f\\u00b0C for 5\\u202fmin. Finally all the samples were transferred to the evaporation chamber. C60 (20\\u202fnm), bathocuproine (BCP, 5\\u202fnm) and silver (75\\u202fnm) were evaporated sequentially at 3\\u202f\\u00d7\\u202f10\\u22127 torr to complete the fabrication process. For semitransparent cells, 200\\u202fnm ITO was sputtered from a 3\\u2033 target (Lesker) at a 100\\u202fW power under Ar pressure of 1.5 mtorr. The active area of devices is 0.12\\u202fcm2 as defined by the overlapped region between the back electrode and the pre-patterned ITO.\\n\\nSEM images were taken with a Hitachi S-4800 high-resolution field-emission microscope. Absorbance spectra of perovskite films were measured by employing a ultraviolet\\u2013visible (UV\\u2013vis) spectrophotometer (PerkinElmer Lambda 1050). Time-resolved photoluminescence (TRPL) was performed as we reported earlier. The kinetic energy spectra of the perovskite films with and without GABr treatment were characterized by an ultraviolet photoelectron spectroscopy (UPS) system (Thermo Scientific, Escalate 250Xi). J-V curves were measured by adopting a Keithley 2400 source meter under AM1.5G (100\\u202fmW/cm2) illumination (PV Measurements Inc.). Photostability measurement was performed at room temperature in ambient air using a Xenon lamp light source (Newport Corporation, USA) equipped with an AM1.5G spectral filter calibrated to 100\\u202fmW/cm2 light intensity. The light intensity was calibrated by a standard silicon solar cell. External quantum efficiency (EQE) spectra from 300\\u202fnm to 800\\u202fnm were obtained with a QE system (PV Measurements Inc.) All the characterizations were measured under the ambient at room temperature.\\nKPFM results were acquired by a Veeco D5000 AFM equipped with a Nanoscope V controller, where the AFM was set up in an Ar-filled glove box with water/oxygen content <0.1\\u202fppm. KPFM measures the contact potential difference between the probe (Nanosensor PPP-EFM, Pt/Ir coated) and sample by probing and nullifying the Coulomb force between the probe and sample. Topographic and potential images were collected simultaneously during the probe scanning. The electrostatic potential of the sample is mapped at a spatial resolution of \\u223c30\\u202fnm and a potential resolution of \\u223c10\\u202fmV. During the measurements, the work function of the probe remains unchanged. In the cross-sectional measurements, the devices were cleaved from the film side to expose the cross section with no further treatment (polishing and ion milling); in the surface potential measurements, the samples were also as deposited with no other special sample preparation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: Cs0.2FA0.8PbBr0.9I2.1,\\n Perovskite_composition_short_form: CsFAPbBrI,\\n Perovskite_additives_compounds: GUBr,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 105.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 5.0,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: F4-TCNQ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 70,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 72,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbI2 (99.99%), CH3NH3I (99.99%), anhydrous chlorobenzene (\\u226599.0%), anhydrous dimethylformamide (DMF) and anhydrous dimethylsulfoxide (DMSO), titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol) and Spiro-OMeTAD (2,29,7,79-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluoren-e, \\u226599.0%) were purchased from Sigma-Aldrich. RuCl3\\u00b75H2O (98.5%), 4-tert-Butylpyridine (t-BP), and Li-bis- (trifluoromethanesulfonyl)imide (Li-TFSI) were purchased from Aladdin reagent. Titanium dioxide nanoparticles (particle size of 30\\u202fnm) were provided by Dyesol All. Solvents were used without any further purification.\\n\\nFTO layers on glass substrates, with a sheet resistance of 8\\u202f\\u03a9/\\u25a1 (Pilkington), were patterned by etching with the Zn powder and 2\\u202fM HCl followed by cleaning with soap and then were cleaned with alkaline detergent, acetone, absolute ethanol and deionized water for 15\\u202fmin, The cleaned substrates were UV-ozone treated for 15\\u202fmin, respectively, before they were used for spin-coating. The TiO2 compact layers were prepared by dissolving titanium diisopropoxide bis(acetylacetonate) solution in ethanol in a 1:10\\u202fvol ratio with mixing RuCl3 in titanium precursor solution in 0.5, 1.0, 2.0, and 5.0\\u202fmol% for the doped films. The TiO2 compact films (undoped and doped) were obtained by spin-coating of precursor solution on the UV-ozone treated substrates at 3000\\u202frpm for 30\\u202fs by annealing at 150\\u202f\\u00b0C for 5\\u202fmin and then sintered in air at 500\\u202f\\u00b0C for 30\\u202fmin resulting in 50\\u202fnm compact layers. Mesoporous TiO2 layer (mass ratio 1:7) was spin-coated at 4000\\u202frpm for 30\\u202fs and then annealed in air at 500\\u202f\\u00b0C for 30\\u202fmin and cooled down to room temperature. MAPbI3 precursor solution was prepared by mixing 159\\u202fmg CH3NH3I, 462\\u202fmg PbI2 in anhydrous DMF: DMSO (9:1, v/v), then filtered with 0.22\\u202f\\u03bcm nylon filter to obtain a clear solution. The MAPbI3 precursor solution was spin-coated on the TiO2 coated substrates at 3000\\u202frpm for 30\\u202fs and 200\\u202f\\u00b5l chlorobenzene was slowly dripped on the surface of the film 10\\u202fs after the beginning of spin-coating. Perovskite layer was annealed at 100\\u202f\\u00b0C for 20\\u202fmin resulting in a thickness of 300\\u202fnm. 72.3\\u202fmg Spiro-OMeTAD, 28.8\\u202f\\u00b5l 4-tert-butylpyridine and 17.5\\u202f\\u00b5l of Li-bis(trifluoromethanesulfonyl)imide solution (520\\u202fmg/ml in acetonitrile) were dissolved in 1\\u202fml chlorobenzene to form Spiro-OMeTAD solution, Spiro-OMeTAD layer was formed sequentially by spin-coating Spiro-OMeTAD solution at 3000\\u202frpm for 30\\u202fs having a thickness of 200\\u202fnm. Finally, Au electrode was deposited using thermal evaporation at a constant evaporation rate of 0.1\\u202fnm/s. Except for the fabrication of TiO2 layer, the whole process is carried out in glove-box under Ar condition at home temperature.\\n\\nThe field emission scanning electron microscope (FESEM) images were obtained on a ZEISS SUPRA55. Energy dispersive spectrometry (EDS, Thermo-NS7, manufacturer) was used to determine the elemental composition. X-ray diffraction (XRD) patterns were collected with a SmartLab from Rigaku at 40\\u202fKv and 150\\u202fmA by using Cu-Ka radiation (\\u03bb\\u202f=\\u202f0.15405\\u202fnm). The valence states of the constituent elements were identified by high resolution X-ray photoelectron spectroscopy (XPS) using Mg K\\u03b1 and h\\u03bd\\u202f=\\u202f1253.6\\u202feV. AFM figures were measured using 300HV scanning force microscope (SEIKO). The photovoltaic performance of PSCs was recorded using a Keithley 4200 source meter with a delay time of 100\\u202fms under one-sun AM 1.5G (100\\u202fmW/cm2) illumination with a solar light simulator (Newport Oriel Sol3A Class AAA, 64023A Simulator), which was calibrated using a NREL standard Si solar cell. The error range of the sun simulator is 1000\\u202f\\u00b1\\u202f3\\u202fW/m2. Hall effect measurement was performed with four contacts van der Pauw method (ECOPIA H S-2000). Hall Effect measurements were conducted with a magnetic field intensity of 0.5\\u202fT and current 0.1\\u202fmA under dark testing environment. EIS measurements were conducted by an electrochemical workstation (CHI660d) (1\\u202fMHz\\u2013100\\u202fHz) and the fitting software was Zview software. The UV\\u2013vis light absorption measurement was performed by using an ultraviolet\\u2013visible (UV\\u2013vis) spectrophotometer (Shimadzu UV-3101 PC). The external quantum efficiency (EQE) measurements were obtained on a Keithley 2000 multimeter as a function of the wavelength from 350 to 800\\u202fnm on the basis of a Spectral Products DK240 monochromator. The active area of the cell is 0.1\\u202fcm2. All samples were measured in air (25\\u202f\\u00b0C).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Ru | Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: 19,\\n Stability_PCE_initial_value: 18.35,\\n Stability_PCE_end_of_experiment: 21,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Anhydrous ethanol (99.9%), chlorobenzene (95%), anhydrous N,N-dimethylformamide (DMF, 99.8%), acetonitrile (99.8%), dimethyl sulfoxide (DMSO, 99.9%), Hydrochloric acid (HCL, AR,35\\u201337%), titanium(IV) isopropoxide (99.9%), Ruthenium chloride hydrate (RuCl3\\u00b7xH2O), formamidinium acetate (99%), hydroiodic acid (57\\u202fwt% in H2O), methyl ammonium (98%), hydrobromic acid (48%). 4-tertbutylpyridine (TBP, 96%), lithium bis-(trifluoromethylsulphonyl) imide (Li-TFSI, 95%), Lead iodide (PbI2, 99.9%), Lead bromide (PbBr2, 99.99%) and Poly(triarylamine) (PTAA) were purchased from Sigma-Aldrich. The TiO2 paste (18 NRD) was purchased from Dyesol.\\n\\nThe FAI and MABr have been synthesized in a previous report with further correction (McMeekin et al., 2016) of dissolving formamidinium acetate powder in a 1.5\\u00d7 molar excess of hydroiodic acid (HI) in an ice bath. For methylammonium bromide, hydrobromic acid (HBr) was slowly added to a methyl ammonium in an ice bath. After the addition of acid, the ice-cold solution was stirred for 120 mins, followed by the evaporation of the solvent using a rotary evaporator at 60\\u202f\\u00b0C, and a yellow-white powder was formed. The powder was later dissolved in ethanol so as to obtain a supersaturated solution. Once completely dissolved, the powder recrystallized using diethyl ether forms white crystals. The powder is further washed with diethyl ether three times and dried overnight in a vacuum oven at 60\\u202f\\u00b0C.\\n\\nFluorine-doped tin oxide (FTO) (8\\u202f\\u03a9\\u202fcm2) was etched with zinc powder and 2\\u202fM aqueous HCl. The etched FTO was cleaned in a soap solution, deionized water, acetone, and isopropanol, each step accompanied by sonication for 10 mins and followed by drying in a nitrogen air. Prior to c-TiO2 deposition, FTO was treated with UV-Ozone for 15\\u202fmin. Then, c-TiO2 film (30\\u202fnm) was deposited by spin-coating from a sol-gel precursor solution consisting of titanium isopropoxide (TTIP) (1\\u202fml) and 2\\u202fM HCl (100\\u202f\\u03bcL) in anhydrous isopropanol (10\\u202fml). The acidic TTIP solution was spin coated at 5000\\u202frpm for 30\\u202fs on cleaned FTO substrate. The substrate was annealed at 150\\u202f\\u00b0C for 15 mins on a hot plate and subsequently annealed in air at 450\\u202f\\u00b0C for 30 mins.\\n\\nA mp-TiO2 film was deposited by spin coating a diluted paste (1:6\\u202fwt ratio, Dyesol 18 NRD: ethanol) (150\\u202f\\u03bcL were poured on 1.5 * 2.5\\u202fcm2 substrate, 4000\\u202frpm, acceleration 3000\\u202frpm for 30\\u202fs) over c-TiO2 film. The substrate was annealed at 150\\u202f\\u00b0C for 10 mins on a hot plate then again in air at 450\\u202f\\u00b0C for 30 mins.\\n\\nThe mp-TiO2 film was treated with different molar concentrations of RuCl3 dissolved in anhydrous ethanol by spin-coating at 4000\\u202frpm for 20\\u202fs (150\\u202f\\u03bcL) under ambient condition, then further annealed at 450\\u202f\\u00b0C for 30 mins under dry air. After slow cooling up to 150\\u202f\\u00b0C, the substrates were transferred to the nitrogen glovebox with <1% humidity for perovskite deposition.\\n\\nThe mixed perovskite film was deposited using the one-step deposition method from the precursor solution containing FAI (1\\u202fM), PbI2 (1.1\\u202fM), MABr (0.2\\u202fM), and PbBr2 (0.2\\u202fM) in anhydrous dimethylformamide/dimethyl sulphoxide (DMF/DMSO) (4:1\\u202fvol ratio). The mixed perovskite precursor solution was spin-coated onto the mp-TiO2 and Ru-TiO2 films at 2000 and 6000\\u202frpm for 10 and 40\\u202fs, respectively, then 120\\u202f\\u03bcL of chlorobenzene as an antisolvent was dropped on the substrate 15\\u202fs prior to the end of the deposition process. The substrate was immediately transferred to a hot plate and annealed at 100\\u202f\\u00b0C for 90 mins.\\n\\nThe solution of poly(triarylamine) (15\\u202fmg, PTAA) in toluene (1.5\\u202fml) mixed with 15\\u202f\\u03bcL solution of lithium bistrifluoromethane sulphonimidate (170\\u202fmg) in acetonitrile (1\\u202fml) and 7.5\\u202f\\u03bcL 4-tert-butylpyridine was spin-coated on top of the perovskite film at 4000\\u202frpm for 30\\u202fs. Finally, 80\\u202fnm of Au counter electrode was deposited by thermal evaporation under high vacuum. The active area of this electrode was fixed at 0.09\\u202fcm2.\\n\\n\\nThe X-ray diffraction spectrometer (Rigaku, Japan) with a Cu k line of 1.5410 \\u00c5 was used to determine phase and crystallinity. The surface and cross-sectional measurements were carried out using a field emission scanning electron microscope (FE-SEM; S-4700, Hitachi). The surface roughnesses of the perovskite thin films were recoded using atomic force microscopy (XE-100 Advanced Scanning Probe Microscope, Park Systems). High-Performance X-ray Photoelectron Spectroscopy (XPS) was used to determine the elements existing within a film. Photoluminescence (PL) spectra were analyzed using a photoluminescence spectrometer (f\\u202f=\\u202f0.5\\u202fm, Acton Research Co., Spectrograph 500i. USA), and an intensified CCD(PI-MAX3) (Princeton Instrument Co., IRY124, USA). The device was illuminated using a solar simulator at AM 1.5G, for which the light intensity was adjusted to that of a calibrated Si solar cell with KG-5 filter to 1 sun intensity (100\\u202fmW cm\\u22122). The external quantum efficiency (EQE) spectra were analyzed as a function of wavelength from 300 to 800\\u202fnm using a Spectral Products DK240 monochromator.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 90,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 2400,\\n Stability_PCE_initial_value: 16.8,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were purchased from Aldrich and used as received, unless otherwise specified. TEM images were recorded using a JEOL JEM-2100 LaB6 HRTEM instrument. UV\\u2013vis absorption spectra were recorded using a Hitachi U-5100 spectrophotometer.\\n\\nSilver nanoprism colloids were prepared according to the literature . Briefly, a solution of sodium citrate (3.0\\u00d710\\u22122 M, 1 mL) and a solution of silver nitrate (1.0\\u00d710\\u22122 M, 1 mL) were added to pure water (97 mL) with rapid stirring. A solution of sodium boronhydride (5.0\\u00d710\\u2212 3 M, 1 mL) was then added dropwise to the mixture, under vigorous magnetic stirring. The solution turned yellow immediately. After stirring for 30 min, the solution was irradiated with a Na lamp (Philips 100-W, \\u03bb=589 nm), the emission spectrum of which is displayed in Fig. S1. The typical power of the light on the solution was approximately 0.22 W cm\\u22122 . The color of the solution changed gradually from yellow to green, eventually turning blue after 3\\u20136 h of irradiation. Blue (\\u03bb max \\u2245700 nm in the extinction spectrum) is the typical color of a colloidal Ag nanoprism solution. The lengths of the sides of the Ag nanoprisms were approximately 70\\u00b120 nm.\\n\\nA solution 200 \\u03bcL sample of 10\\u22123 M PVP (10\\u22123 M, 200 \\u00b5L) was added into 1.8 mL of a solution of the as-prepared Ag nanoprism colloid solution (1.8 mL) in a vial. After 20 min, a solution of 200 \\u03bcL of 10\\u22123 M KBr (10\\u22123 M, 200 \\u00b5L) was added into the PVP-treated colloid solution to initiate the etching process. The color of the colloidal solution changed gradually from blue to indigo, purple, purplish red, pink, orange, and yellow over a period of approximately 30 min. These color changes of the Ag colloids were correlated to the shape transformations of the nanomaterials\\u2014from Ag nanoprisms to round Ag NPLs\\u2014in the presence of halide ions. Time-dependent UV\\u2013vis spectra and TEM images were recorded to trace the shape evolutions of silver nanostructures. All the UV\\u2013vis spectra were recorded in a Hitachi U-5100 spectrometer. Typically suitable protecting reagents, such as MHA, which have been found to form a self-assembly monolayers immediately on the surfaces of Ag NPLs surface are required to prevent the further bromide-mediated sculpturing process caused by the bromide ions . Hence, a 100 \\u03bcL sample of 10\\u2212 4 M MHA was added into the colloid solution to terminate the etching reaction process when the solution displayed the desired color. Finally, this approach, highly stable Ag nanostructures with the desired SPR wavelengths were obtained.\\n\\n\\nAll PV cells were prepared using the following device fabrication procedure. Glass/ITO substrates [Sanyo, Japan (8 \\u03a9/\\u25a1)] were sequentially patterned lithographically, cleaned with detergent, ultrasonicated in acetone and isopropyl alcohol, dried on a hot plate at 140 \\u00b0C for 10 min, and treated with oxygen plasma for 5 min. PEDOT:PSS (Baytron P-VP AI4083) was passed through a 0.45 \\u00b5m filter; different ratios of Ag NPLs were added prior to deposition on ITO (thickness: ca. 45 nm) through spin-coating at 3000 rpm in air, the sample was then dried at 140 \\u00b0C for 20 min in a glove box. Blends of P3HT or PTB7 with PCBM or PC71BM at defined ratios (1:1 for P3HT; 1:1.5 for PTB7) were stirred overnight in o-DCB, filtered through a 0.2-\\u00b5m polytetrafluoroethylene (PTFE) filter, and then spin-coated (600\\u20131000 rpm, 30 s) on top of the PEDOT:PSS/Ag NPLs layer. The device was completed by depositing a 30-nm-thick layer of Ca and a 100-nm-thick layer of Al at pressures of less than 10\\u2212 6 Torr. PVSK cells were prepared using the following device fabrication procedure. The PVSK precursor solution was prepared by dissolving MAI and lead (II) chloride at ratio of 3:1 (molar ratio) at 25 wt% in DMF and continuously stirring at 60 \\u00b0C in the dark overnight. PVSK devices, having the layered configuration glass/ITO/PEDOT:PSS (w/ or w/o Ag NPLs)/CH3NH3PbI3\\u2212xClx /PC61BM/Al, were fabricated using methods similar to those reported previously (Fig. 1c) . Prior to the deposition of the PVSK layer, the PEDOT:PSS film was preheated at 60 \\u00b0C for 5 min. The precursor solution was also preheated at 60 \\u00b0C for 5 min and then deposited on top of the PEDOT:PSS. PCBM was spin-coated (2000 rpm) from a chlorobenzene solution (10 mg mL\\u2212 1). The layers of Al (100 nm) were deposited thermally under vacuum. The active area of the all the devices was 10 mm2. The cell performance was measured inside a glove box. The current\\u2013voltage (I\\u2013V) properties of the OPV devices were measured using a computer-controlled Keithley 2400 source measurement unit (SMU) and a Newport solar simulator (Oriel\\u00ae Sol2A Class ABA Solar Simulators) under AM 1.5 illumination (100 mW cm\\u22122). The illumination intensity was calibrated using a standard Si reference cell and a KG-5 filter. EQEs were measured using an Enlitech QE-R spectral response measurement system to calibrate the current densities of the devices. The morphologies of the polymer films were analyzed through AFM using a VEECO DICP-II instrument operated in the tapping mode at ambient temperature; the etched Si probe exhibited a resonant frequency of 131 kHz and a spring constant of 11 N m\\u22121. The stability of the devices was tested while the samples were placed inside the glove box. We used an OSRM halogen lamp [HAL PRO CL B 30 W 230 V E14] as light source; the intensity of light irradiated on devices was set at 2000 lux.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 23.0; 23.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: 8,\\n Stability_PCE_end_of_experiment: 100,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite absorber material: 15\\u2009g formamidine acetate and 30\\u2009mL HI (57\\u2009wt% in water) were dissolved in 100\\u2009mL ethanol at 0\\u2009\\u00b0C for 2\\u2009h with stirring to obtain HC(NH2)2I. A solution of HC(NH2)2I was dried using rotary evaporator at 50\\u2009\\u00b0C for 1\\u2009h. Following recrystallization from ethanol, white crystals were washed with diethyl ether. To synthesize CH3NH3Br, 11\\u2009mL methylamine (33\\u2009wt% in water) and 10\\u2009mL HBr (48\\u2009wt% in water) were mixed in 100\\u2009mL ethanol at 0\\u2009\\u00b0C for 2\\u2009h with stirring. Prepared HC(NH2)2I (or CH3NH3Br) and PbI2 (or PbBr2) were dissolved at room temperature in dimethylformamide (DMF): dimethyl sulfoxide (DMSO) mixed solvent (1:0.25 (v/v)) to obtain 1.2\\u2009M HC(NH2)2PbI3 (or CH3NH3Br3) solution. To prepare the absorption layer precursor solution, HC(NH2)2PbI3 and CH3NH3Br3 solution were mixed with the specific volume ratio for (HC(NH2)2PbI3)0.85(CH3NH3PbBr3)0.15. And then extra PbI2 (5\\u2009mol% to HC(NH2)2PbI3) were dissolved in the synthesized (HC(NH2)2PbI3)0.85(CH3NH3PbBr3)0.15 solution by heating at 60\\u2009\\u00b0C for 30\\u2009min. Materials used in this work were purchased from Alfa Aesar or Lumtec or Sigma-Aldrich and were not purified.\\n\\nTo fabricated mesoporous solar cell for the experimental work, firstly, a compact TiO2 layer (c-TiO2) was deposited by spray pyrolysis (~\\u200950\\u2009nm) using 20\\u2009mM titanium diisopropoxide bis(acetylacetonate) solution at 450\\u2009\\u00b0C on the clean FTO glass (TEC8). After the deposition of c-TiO2 layer, 150\\u2009mg/mL of mesoporous TiO2 paste (m-TiO2, Dyesol 30 NR-D) in ethanol was spin-coated at 5000\\u2009rpm (acceleration of 2000\\u2009rpm\\u2009s-1) for 10\\u2009s. The deposited substrates were heated at 100\\u2009\\u00b0C for 10\\u2009min followed by sintering at 500\\u2009\\u00b0C for 30\\u2009min. The prepared perovskite solution was spun at 2000\\u2009rpm (acceleration of 200\\u2009rpm\\u2009s-1) and 6000\\u2009rpm (acceleration of 2000\\u2009rpm\\u2009s-1) for 10\\u2009s and 30\\u2009s. The anti-solvent chlorobenzene was drop-casted (110\\u2009mL) during the last 20\\u2009s of the second spin-coating step. The coated perovskite film was dried on a hot plate at 100\\u2009\\u00b0C for 20\\u2009min. For the deposition of hole transport layer, a solution containing 41.6\\u2009mg of spiro-OMeTAD, 7.5\\u2009\\u00b5L of a 500\\u2009mg/mL lithium bis (trifluoromethylsulphonyl)-imide (Li-TFSI) in acetonitrile and 16.9\\u2009\\u00b5L of 4-tert-butylpyridine (tBP) in 0.5\\u2009mL chlorobenzene was spin-coated respectively on the perovskite/m-TiO2/bl-TiO2/FTO substrate at 2000\\u2009rpm (acceleration of 1200\\u2009rpm\\u2009s-1) for 20\\u2009s. Alternatively a solution containing 15\\u2009mg of PTAA, 15\\u2009\\u00b5L of a 170\\u2009mg/1\\u2009mL Li-TFSI in acetonitrile and 7.5\\u2009\\u00b5L of tBP in 1.5\\u2009mL toluene was deposited using the same conditions. All films on m-TiO2 were prepared in nitrogen filled glovebox. Finally, 100\\u2009nm of gold electrode was deposited by thermal evaporation.\\n\\nTwo kinds of ALD processes were employed in this work: 1) thermal ALD (Th-ALD), and plasma ALD (Pl-ALD). Th-ALD used Trimethylaluminum (TMA) and H2O (Classic, CN1, South Korea), and Pl-ALD employed TMA and O2 plasma as precursors (Lucida M200-PL, NCD, South Korea). Th-ALD procedure consists of 4 steps: (1) TMA was pulsed into reaction chamber for 0.1\\u2009s using N2 gas with 500 sccm after sample loading, (2) Excess TMA and methane reaction products were purged by N2 for 5\\u2009s with 500 sccm, (3) Water vapor was pulsed into reaction chamber for 0.1\\u2009s by N2 with 500 sccm, Finally (4) N2 was purged to remove excess water vapor for 5\\u2009s with 500 sccm. For the Pl-ALD process, the procedure is similar to that of Th-ALD. Pl-ALD process consists of 4 steps: (1) TMA was injected and pulsed into reaction chamber for 0.2\\u2009s using Ar gas with 100 sccm after sample loading, (2) Excess TMA precursor was purged by Ar for 15\\u2009s with 300 sccm, (3) O2 reactant was injected for 2\\u2009s by Ar with 200 sccm and O2 plasma was generated with 100\\u2009W of RF power and Ar gas which was charge of improving generation of plasma were introduced for 3\\u2009s with 100 sccm, (4) Excess reactant was purged by Ar for 15 with 300 sccm. To investigate the effect of temperature on PSCs, three Th-ALD operating temperatures at 95\\u2009\\u00b0C, 105\\u2009\\u00b0C, 120\\u2009\\u00b0C to deposit 50\\u2009nm of Al2O3 in the study. Once the desired temperature is chosen, e.g., at 95\\u2009\\u00b0C, 50\\u2009nm thick Al2O3 were fabricated on PEN films using the two different ALD processes for the measurement of WVTR. The WVTR values were measured with AQUATRON Model 2 (Mocon Co., USA).\\n\\nThe J\\u2013V measurements were performed using a solar cell I\\u2013V testing system (LAB 200, McScence, Korea) under illumination power of 100\\u2009mW/cm2 by an AM1.5\\u2009G solar simulator (Oriel model 94023A) with 0.159\\u2009cm2 aperture and a scan rate of 1.2\\u2009V/s. X-ray diffraction (XRD) patterns were measured using a XRD-6100 (SHIMADZU, JAPAN) with a Cu K\\u03b1 radiation source (\\u03bb\\u2009=\\u20090.1541\\u2009nm) at 30\\u2009kV and 30\\u2009mA. Reflectance (R) and transmittance (T) were measured using a Varian Cary UV\\u2013VIS\\u2013NIR spectrophotometer in the 300\\u2013900\\u2009nm wavelength range. Field emission scanning electron microscopy (ESEM\\u2013FEG XL30, FEI, Holland) was employed to investigate the effect of thermal stress on the morphology and structure of the perovskite. To carry out transmission electron microscopy (TEM) analysis, samples mounted on Cu girds were prepared using Focused Ion beam. The prepared sample was measured with JEM-2100F (JEOL LTD) at operating 200\\u2009kV equipped with EDS (TEM 250, Oxford Instruments). Stability tests were carried out in two kinds of conditions. These include: (a) 65\\u2009\\u00b0C-85%RH (SE-CT-02, SUKSAN Tech. South Korea), and (b) ambient condition.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 65.0; 65.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 350,\\n Stability_PCE_initial_value: 15.312,\\n Stability_PCE_end_of_experiment: 55,\\n Cell_area_measured: 0.159,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The SnO2 colloid was purchased from Alfa Aesar (tin(IV) oxide). Methylammonium iodide (MAI), methylammonium bromide (MABr), and cesium iodide (CsI) were purchased from Xi'an Polymer Light Technology Corp. Formamidinium iodide (FAI) was purchased from Dyesol Ltd. (Queanbeyan, Australia). Lead iodide (PbI2, 99%), lead bromide (PbBr2, 99.999%), guanidinium bromide (GABr, 99%), N,N-dimethylformamide (DMF, 99.8%), dimethyl sulfoxide (DMSO, 99.9%), and chlorobenzene (99.8%) were purchased from Sigma-Aldrich.\\n\\nDevices were fabricated on FTO substrates (15 \\u03a9 sq\\u22121) with dimensions of 20 \\u00d7 20 mm. The substrates were thoroughly cleaned with a detergent solution, acetone, and isopropanol, and finally treated in a plasma cleaner for 5 min. Then, a layer of SnO2 (purchased from Alfa Aesar) was deposited in ambient air as the electron transport layer at a speed of 4000 rpm for 30 s and then annealed at 140 \\u00b0C for 20 min. After cooling to room temperature, the substrates were transferred to a nitrogen filled glove box.\\nTo prepare the perovskite precursor solution, FAI (1 M), PbI2 (1.05 M), MABr (0.2(1 \\u2212 x) M), GABr (0.2x M) and PbBr2 (0.2 M) were first dissolved in anhydrous DMF:DMSO 4:1 (v:v) for FA/MA/GA solution, where x ranges from 0 to 1. Then an appropriate amount of CsI (1.5 M in DMSO) was added to the FA/MA/GA solution for the target quadruple cation based CsFAMA1\\u2212xGAx perovskite precursor. Before use, all perovskite precursors were stirred at room temperature for 3 hours in a glove box and filtered with a 0.45 \\u03bcm polytetrafluoroethylene (PTFE) filter.\\nThen, 60 \\u03bcL of the prepared perovskite precursor was dropped on the substrate and spin-coated at 600 rpm for 5 s and then at 4000 rpm for 40 s. During the second procedure, 150 \\u03bcL of toluene was dropped on the spinning substrate 15 s before the program ended. The resulting films were transferred to a hot plate at 120 \\u00b0C and dried for 15 min. Subsequently, a traditional spiro-OMeTAD layer, which consisted of 72.3 mg of spiro-OMeTAD, 28.8 \\u03bcL of 4-tert-butylpyridine, 17.5 \\u03bcL of lithium-bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg of Li-TFSI in 1 mL of acetonitrile), and 1 mL of chlorobenzene, was deposited on the perovskite films as the hole transport layer. Finally, an approximately 80 nm thick Au electrode was fabricated using a shadow mask under high vacuum by thermal evaporation.\\n\\nCurrent density\\u2013voltage (J\\u2013V) curves of the devices were measured using a solar simulator (Newport Oriel Sol 3A Class AAA, 64023A) equipped with a 450 W xenon lamp (Oriel, USA) and a Keithley 2400 source meter. The light intensity was calibrated to AM 1.5G (100 mW cm\\u22122) by using a reference Si solar cell (Newport). The devices were masked with a metal aperture of 0.06 cm\\u22122 to define the active area. The J\\u2013V measurements were all conducted in ambient air with a scanning protocol of 1.2 to \\u22120.05 V for the reverse scan (\\u22120.05 to 1.2 V for the forward scan) with a 24 mV voltage step.\\n\\nFor long-term stability, w/o GA and 0.2 GA films or corresponding unencapsulated devices were stored in a dry cabinet with 25% humidity at 25 \\u00b0C in the dark. The UV-vis absorption and XRD of the films were measured every 7 days. The J\\u2013V curves of the devices were recorded every day. Thermal stability was studied by exposing the devices to the ambient environment of 80 \\u00b0C and 40% humidity and measuring the J\\u2013V curves every day. For light-soaking stability test, unencapsulated devices were exposed to continuous 1 sun illumination generated by an LED lamp without UV light. The J\\u2013V curves of the devices were recorded every 5 or 10 min. Between each measurement, the cells were maintained at the maximum power point.\\n\\nThe XRD patterns (2\\u03b8 scans) were obtained on a Bruker Advanced D8 X-ray diffractometer using Cu K\\u03b1 (\\u03bb = 0.154 nm) radiation. The compositions and chemical environments of the films were analyzed by X-ray photoelectron spectroscopy (PHI Model 5802). UV-vis diffuse reflectance spectroscopy (UV-vis-DRS, Shimadzu UV-3600) was used to collect the absorbance spectra of the perovskite films. Steady state photoluminescence (PL) spectra were recorded on a Shimadzu RF-5301pc with an excitation wavelength of 523 nm. A field-emission scanning electron microscope (FESEM, JEOL 7100F) was used to study the surface and cross-section morphology. Grazing incident XRD (GIXRD) patterns were obtained by using a Rigaku Smartlab X-ray diffractometer with the incidence angle ranging from 0.5\\u00b0 to 7\\u00b0. The external quantum efficiency (EQE) spectra were measured under a constant white light supplied by an array of white-light emitting diodes. The excitation beam from a 300 W xenon lamp was focused through a double-monochromator and chopped at 10 Hz. The monochromatic light intensity for the measurement was calibrated using a reference silicon photodiode. Time-resolved photoluminescence spectra were measured using a PL system (DW-PLE03). TGA analysis was conducted using a thermogravimetric analyzer (TGA/DSC 1 STARe System). The electrochemical impedance spectroscopy measurements were carried out by using an electrochemical workstation (Zennium Zahner, Germany). A bias of the open-circuit voltage was applied during the measurement at frequencies ranging from 1 MHz to 1 Hz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.788GU0.032MA0.129PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAGUMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TPB,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Ambient,\\n Stability_time_total_exposure: 5,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 88,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the materials and chemicals in our work were used as received without further purification, including PEDOT:PSS (Clevious PVP. AL 4083, Heraeus, 1 g mL\\u22121), methylamine iodide (MAI, 99.5% Shanghai MaterWin New Materials Co., Ltd.), lead(II) iodide (PbI2, 99.99%, TCI (Shanghai) Development Co., Ltd.), ammonium rhodanate (NH4SCN, 99.99%, Sigma-Aldrich), ammonium iodide (NH4I), lead rhodanide (Pb(SCN)2, 99.99%, Sigma-Aldrich), PC61BM, lithium fluoride (LiF, 99.99%, Sigma-Aldrich), N,N-dimethylformamide (DMF, anhydrous, 99.7%, Sigma-Aldrich), dimethyl sulfoxide (DMSO, anhydrous, 99.7%, Sigma-Aldrich), and chlorobenzene (CB, anhydrous, 99.9%, Sigma-Aldrich).\\n\\nIndium tin oxide (ITO) substrates (sheet resistance of 15 \\u03a9 sq\\u22121) were cleaned with Hellmanex III detergent in DI water, DI water, acetone, ethanol and isopropyl alcohol, respectively, and dried in an oven overnight. Before use, the ITO substrates were cleaned with UV-O3 for 15 min and PEDOT:PSS solution was filtered with a 0.45 \\u03bcm nylon filter. Then, 50 \\u03bcL PEDOT:PSS was spin-coated onto the ITO substrates at 5000 rpm for 50 s and annealed at 120 \\u00b0C for 30 min in air atmosphere. The perovskite precursor solution was prepared by dissolving 0.1 mmol PbI2 (461 mg) and 0.1 mmol (159 mg) in 1 mL DMSO and DMF mixed solvent (VDMSO:VDMF = 1:4), and stirring at 60 \\u00b0C for 1 h. For additive doping, NH4SCN was added to the perovskite precursor solution at a concentration of 2% (1.52 mg), 5% (3.80 mg), 10% (7.60 mg), 13% (9.88 mg), 15% (11.40 mg), 17% (12.92 mg) and 20% (15.20 mg) (molar ratio, the proportion of all additives is mole ratio). The perovskite precursor solution was coated onto the PEDOT:PSS substrate via spin-coating at 1000 rpm for 10 s and 4000 rpm for 30 s. Subsequently, in the second spin-coating process, 250 \\u03bcL chlorobenzene (CB) was used to wash the perovskite thin film after 10 s. After the end of the spin-coating, the films were annealed at 100 \\u00b0C for 10 min. A solution of 20 mg mL\\u22121 PCBM dissolved in CB was spin-coated onto the perovskite thin films at 1000 rpm for 60 s. Finally, 1 nm LiF and 80 nm aluminum layers were evaporated under 3 \\u00d7 10\\u22124 Pa at a rate of about 0.01 \\u00c5 s\\u22121 and 1 \\u00c5 s\\u22121, respectively.\\n\\nUV-vis absorption was measured on a Shimadzu UV-1750 UV-Visible spectrophotometer. Steady-state and time-resolved photoluminescence spectra were measured with a Hitachi F-4600 spectrofluorometer and Edinburgh FS5-TCSPC, respectively. All AFM images were obtained with a Park XE-70 with an area of 5 \\u03bcm \\u00d7 5 \\u03bcm. Top-view SEM images were obtained using a Hitachi S-4800. XRD patterns were collected with an X-ray diffractometer (Smartlab 3 kW). The device characteristics were measured under AM 1.5G illumination using an Enlitech SS-F5-3A solar simulator, and the J\\u2013V characteristics were measured using the J\\u2013V sweep software developed by Enlitech Ltd. and a Keithley 2400 source/meter unit. Current\\u2013voltage curves were measured in the forward scan range of \\u22120.1 to 1.1 V and the reverse scan from 1.1 to \\u22120.1 V. For stability testing, the films and devices were placed in air with humidity of around 70%.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: PbC2N2S2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 240,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The inverted (p\\u2013i\\u2013n) planar structure perovskite solar cells consisted of ITO/PTAA/PFN/perovskite/PCBM/BCP/top electrode. The top electrode was varied as described in the manuscript. The devices were fabricated by firstly cleaning ITO substrates in acetone, soap, water, acetone and then isopropanol using ultrasonics, drying under a N2 stream and finally exposing to UV-ozone treatment immediately before use. PTAA (2 mg mL\\u22121 in chlorobenzene) was spin-coated onto the cleaned ITO substrate at 3000 rpm for 20 seconds. The perovskite solution, 1.5 M MAPbI3 in DMF/DMSO (8.9:1.1), was then spin-coated on the substrate at 4000 rpm for 30 seconds. After 7 seconds of spinning 0.4 mL diethyl ether was dripped onto the substrate. The substrate was then annealed at 60 \\u00b0C for 1 minute and then 100 \\u00b0C for 30 minutes. PCBM solution (30 mg mL\\u22121) was spin-coated on the substrate at 2000 rpm for 20 seconds. BCP (0.5 mg mL\\u22121) was then spin coated on the substrate at 4000 rpm for 20 seconds. Finally, 100 nm of Al, Ag or Cu was thermally evaporated as a top electrode, in the case of bilayer electrodes 10 nm Cu and 100 nm Ag were thermally evaporated in sequence without breaking vacuum.\\n\\nThe J\\u2013V characteristics were measured under Air Mass 1.5G global (AM 1.5G) illumination (Xenon lamp) at 1 sun intensity, calibrated by a certificated silicon reference cell from National Renewable Energy Laboratory (NREL). The device stability measurements were performed in ambient air under 1 sun illumination provided by an LED light source. The intensity of the LED light was calibrated by matching the Jsc of devices measured using the xenon lamp. The devices were loaded at 0.8 V, which is close to maximum power point, and their J\\u2013V characteristics measured every 5 hours.\\n\\nA LEO Gemini 1525 Field Emission Scanning Electron Microscope was used to obtain SEM images. The sample was coated with 5 nm chromium. Working distance was set at 5 mm, with the accelerating voltage kept below 5 kV.\\n\\nX-ray diffraction (XRD) profiles of perovskite films were obtained with a X'Pert Powder diffractometer (PANalytical) using K line of Cu X-ray source. The diffraction patterns cover a 2\\u03b8 range of 10\\u201350\\u00b0, with a step size of 0.016\\u00b0.\\n\\nToF-SIMS was performed using the IONTOF-TOFSIMS5 instrument. An O2 1 kV (\\u223c230 nA) sputter beam, with a raster size of 300 \\u03bcm \\u00d7 300 \\u03bcm, for its uniform sputtering rates and minimization of damage accumulation, was used. For the generation of secondary ions, a Bi3+ 25 kV (\\u223c0.5 pA) primary ion beam in the high-current bunched mode (HCBM) for higher mass resolution was used, in which a 150 \\u03bcm \\u00d7 150 \\u03bcm analysis area was centered within the sputter crater. Measurements were performed in the interlaced mode (no pause between sputtering and analysis cycles)-total ion images were closely observed to ensure no sample charging took place. The same mass calibration and mass fragment peak list were applied to all mass spectra and depth profiles, respectively, before analysis.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Undoped | Undoped,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60; 100,\\n Perovskite_deposition_thermal_annealing_time: 1.0; 30.0,\\n HTL_stack_sequence: PTAA | PFN,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: Undoped,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 60,\\n Stability_PCE_initial_value: 18.8,\\n Stability_PCE_end_of_experiment: 11,\\n Cell_area_measured: ,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium tetra-iso-propanoate (97%), 1-butanol (99.9%), hydroiodic acid (57 wt% in water), and methylamine (40 wt% in water) were purchased from Sigma-Aldrich and used as received without any purification. Anhydrous N,N-dimethyl-formamide (DMF) and lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) (99%) were purchased from J&K. 2,2\\u2032,7,7\\u2032-Tetrakis(N,N-di-p-methoxy-phenylamine)-9,9-spirobifluorene (Spiro-OMeTAD), lead(II) iodide and tert-butyl pyridine (>96.0%) were purchased from Chemlin Chemical Industry Co., Ltd (Nanjing, China), Alfa Aesar and TCI, respectively.\\nX-ray diffraction (XRD) was carried out by using a Bruker X-ray diffractometer with Cu K\\u03b1 as the radiation source. UV-visible (ultraviolet-visible) absorption spectra were obtained on a PerkinElmer UV-vis spectrometer model Lambda 750. SEM (scanning electron microscope) images were acquired by using an S-4800 (Hitachi) field-emission scanning electron microscope (FESEM). Photoluminescence (PL) spectra were obtained using a PerkinElmer-LS55. Time resolved PL spectra were recorded on a PL spectrometer FLS 900 (Edinburgh Instruments), excited with a picosecond pulsed diode laser (EPL-445) and measured at 775 nm after excitation at 445 nm. XPS (X-ray photoelectron spectroscopy) and UPS (ultraviolet photoelectron spectroscopy) were performed using a Kratos AXIS UTRADLD UPS/XPS system (Kratos analytical, Manchester, UK). XPS studies were performed using a monochromated Al K\\u03b1 (1486.6 eV) X-ray source. The UPS measurement is carried out on an integrated ultra-high vacuum system (3.0 \\u00d7 10\\u22128 Torr) using the He(I) (21.22 eV) line in order to shift the spectra from the spectrometer threshold. Contact angles were measured using an OCA20 instrument (Data-Physics, Germany), and the system was maintained at ambient temperature and saturated humidity. In each measurement, a 2 \\u03bcL droplet of water was dispensed onto the substrates under investigation. The average contact angle value was obtained from three different positions of the same sample.\\n\\nThe thermo-cleavable fullerene DBMD was synthesized using the method described elsewhere.\\n\\nMethylammonium iodide (MAI, CH3NH3I) was prepared according to a previously published method. Perovskite precursor solution was prepared referring to a modified one-step procedure. In brief, CH3NH3I and PbI2 (1:1, mol/mol) were dissolved in anhydrous dimethylformamide (DMF) at a concentration of 320 mg mL\\u22121. 25.3 mg mL\\u22121 NH4Cl was used as an additive to facilitate the formation of a high-quality perovskite crystal. For the sake of characterization, perovskite films were prepared by spin coating the mixed solution onto c-TiO2 or c-TiO2/MCA coated fluorine doped tin oxide (FTO) substrates at 3000 rpm for 60 s, and the substrates were heated at 55 \\u00b0C for 15 min. The obtained films were investigated by UV-visible absorption spectroscopy, XRD and X-ray photoelectron spectroscopy (XPS).\\n\\nFor the device fabrication, first FTO coated glass substrates (15 \\u00d7 20 mm, 15 \\u03a9 sq\\u22121 resistance) were etched with zinc powder and HCl (2 M). Then these FTO substrates were cleaned by ultrasonication in detergent, deionized water, acetone, and isopropanol sequentially. Afterwards, FTO glasses were treated with an alkaline solution (with the volume ratio of H2O:H2O2:NH3 (aq) = 5:1:1) at 160 \\u00b0C for 40 min, and then washed with deionized water several times to remove the residual alkaline solution. The c-TiO2 ETL was made by subsequently spin-coating 1.0 M titanium tetra-iso-propanoate 1-butanol solution (containing 1.0 M HCl) onto FTO substrates at 3000 rpm for 60 s. Then the substrates were dried at 125 \\u00b0C to remove the solvent and sintered at 500 \\u00b0C for 60 min. After the substrates cooled down to room temperature, 9 mg mL\\u22121 DBMD solution in 1,2-dichlorobenzene (DCB) was spin-coated (2500 rpm for 60 s) on the c-TiO2 layer. The DBMD-coated film was heated at 170 \\u00b0C for 10 min to induce thermal cleavage of tertiary alkyl ester to form the MCA film. The as-prepared perovskite precursor solution was spin-coated onto a c-TiO2 (or c-TiO2/MCA) layer at 2500 rpm for 60 s, and the substrates were heated at 55 \\u00b0C for 15 min. 1 mL of Spiro-OMeTAD solution (80 mg mL\\u22121 in chlorobenzene), 28.8 \\u03bcL of 4-tert-butyl pyridine and 17.5 \\u03bcL of Li-TFSI solution (520 mg Li-TFSI in 1 mL acetonitrile) were mixed and used as the precursor for the hole transport layer (HTL). The above doped Spiro-OMeTAD solution was deposited on the pre-prepared CH3NH3PbI3 perovskite layer by spin coating at 4000 rpm for 30 s. Finally, the Ag counter electrode was deposited by thermal evaporation on the HTL layer at a pressure below 10\\u22126 Torr. All the devices were kept overnight in air for the full doping of Spiro-OMeTAD via oxidation. The device was measured in nitrogen with an effective area of 0.04 cm2. J\\u2013V (current density\\u2013voltage) characteristics were recorded at room temperature using an Agilent B2902A Source Meter under the illumination of an AM 1.5G AAA class solar simulator (model XES-301S, SAN-EI) with an intensity of 100 mW cm\\u22122 and the white light intensity was calibrated with a standard single-crystal Si solar cell.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 55,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 336,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead(II) iodide (PbI2, 99.99%) was purchased from Xi\\u2019an polymer Ltd (Xian, China). Methylammonium iodide (MAl) was synthesized according our previous method. Poly[N,N\\u2032-bis(4-butylphenyl)-N,N\\u2032-bisphenylbenzidine] (PolyTPD) and phenyl-C60-butyric acid methyl ester (PCBM) were purchased from Luminescence Technology. Zirconium acetylacetonate (ZrAcac) was purchased from Sigma-Aldrich (USA). All solvents were purchased from Sigma-Aldrich and used as received. The additive DAGCl (1,3-diaminoguanidine monohydrochloride) was purchased from Aladdin (China).\\n\\nPre-patterned ITO glass was sequentially cleaned by ultrasonication in deionized water, ethanol, acetone and isopropyl alcohol for 10 min each, and further treated with ultraviolet-ozone for 10 min to remove any organic contaminants. A PolyTPD layer was deposited by spin-coating a 1.8 mg ml\\u22121 CB solution at 3000 rpm and subsequently annealing at 110 \\u00b0C for 10 min. The perovskite layer was deposited through a two-step sequential deposition method. The precursor solution of the first layer was prepared by dissolving PbI2:MAl (1.3 M:0.3 M) and different concentrations of DAGCl (wt% of MAI) in the solvent mixture made of anhydrous DMF and dimethyl sulfoxide (9:1, v/v), which was then spin-coated onto PolyTPD at 6000 rpm for 15 s. Immediately following this, the second step is the deposition of MAl (0.2 M in isopropanol) on top of the previous layer by spin coating at 3700 rpm for 45 s. The precursor film was then annealed at 100 \\u00b0C for 30 min to convert to perovskite. The PCBM layer was then cast on by spin coating from a 15 mg ml\\u22121 CB solution at 1000 rpm for 30 s. A ZrAcac interlayer was then deposited by spin coating at 5000 rpm for 30 s from its 1 mg ml\\u22121 methanol solution. A 100 nm Ag layer was then deposited via thermal evaporation at high vacuum to finish the device fabrication.\\n\\nThe current density\\u2013voltage (J\\u2013V) curves of devices were measured in ambient conditions under simulated sunlight (100 mW cm\\u22122) using a Newport 3A solar simulator, and the light intensity was calibrated with a silicon solar cell certified by the National Renewable Energy Laboratory (NREL, China). J\\u2013V characteristics were recorded using a J\\u2013V sweep software developed by Ossila Ltd (UK) and a Keithley (USA) 2612B source meter unit. The devices were masked with a metal aperture to accurately define the test area on each pixel and to eliminate the influence of any edge effects. The morphology patterns were obtained by SEM (Hitachi S4800, Japan). GIWAXS measurements were obtained using the beamline BL14B1 at the Shanghai Synchrotron Radiation Facility in China. The steady-state PL spectra were obtained by a PL microscopic spectrometer (Flex One, Zolix, China) using a 532 nm CW laser as the excitation source. The absorption spectra of the perovskite were obtained by using a UV-vis spectrophotometer (Hitachi U-3900H, Japan). Impedance, capacitance\\u2013voltage and IMVS measurements were obtained using a ModuLab XM electrochemical workstation (AMETEK, UK), and the tests were performed under a series of voltages with the amplitude of 10 mV, in the frequency range from 1 MHz to 100 Hz, under 1 sun illumination. Equivalent circuit simulations were fitted using the software package ZView (Scribner, USA). EQE was measured with an EQE system (Zolix, China) equipped with a standard Si diode. The monochromatic beam was generated from a 150 W xenon lamp.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Zr(acac)4,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: DAGCl,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 30.0,\\n HTL_stack_sequence: PolyTPD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 480,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless specified, all the materials were purchased from Sigma-Aldrich or Alfa Aesar and used without further purification. Fluorine-doped tin oxide (FTO) coated glasses (sheet resistance \\u223c7 \\u03a9 sq\\u22121) were purchased from Nippon Sheet Glass Co., Ltd. (Tokyo, Japan). PCBM was purchased from Luminescence Technology Corp. Spiro-OMeTAD was purchased from Borun Chemical Co., Ltd. (Zhejiang, China). BAI was purchased from Polymer Light Co. Ltd (Xi'an China).\\n\\nFTO coated glasses were partially etched with Zn powder and 2 M HCl. Then the etched substrates were cleaned with deionized water, acetone, ethanol and isopropanol sequentially. Before use, the substrates were treated with O2-plasma for 3 min to make them well hydrophilic. The TiO2 compact layers were deposited by spin-coating a solution of titanium isopropoxide in ethanol at 2000 rpm for 60 s, and annealed at 500 \\u00b0C for 30 min. Then an 8 mg mL\\u22121 PCBM solution in CB was spin-coated on the top of the TiO2 compact layer at 4000 rpm for 40 s in a N2-filled glove box. The 0.9 M CsPbI2Br precursor solution was prepared by dissolving CsI, PbI2 and PbBr2 in a 1 mL DMF/DMSO (volume ratio 4:1) mixture with a 1:0.5:0.5 ratio. Perovskite films were deposited on FTO/TiO2/PCBM substrates by spin-coating the precursor solution at 1000 r for 10 s and 4000 r for 45 s. During the second step, chlorobenzene was quickly dropped onto the film at the last 15 s. The samples were placed at room temperature for 15 min and then annealed at 150 \\u00b0C for 1 min. For BAI treatment, 1, 3, 5 or 7 mg BAI and 10 mL DMSO were added to 990 mL CB. Then 100 \\u03bcL of the solution was dropped within 2\\u20133 seconds on the perovskite film spinning at 4000 r, and the samples were annealed at 150 \\u00b0C for 1 min. Subsequently, the spiro-OMeTAD precursor solution, prepared by dissolving 72.3 mg spiro-OMeTAD (2,2,7,7\\u2032-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9\\u2032-spirobifluorene), 28.8 \\u03bcL TBP (4-tert-butylpyridine) and 17.5 \\u03bcL LiTFSI solution (520 mg mL\\u22121 bis(trifluoromethane) sulfonamide lithium salt in acetonitrile) in 1 mL CB, was spin-coated at 4000 rpm for 40 s to form the hole transport layer. Finally, 80 nm Au was thermally evaporated on the top of the device as the electrode.\\n\\nThe crystalline structures of the perovskite films were characterized by X-ray diffraction (XRD, D8 Advance diffractometer, Bruker, Germany, Cu-K\\u03b1, \\u03bb = 1.5406 \\u00c5). The morphology of the films was observed with a scanning electron microscope (SEM, Merlin, Zeiss, Germany). The XPS spectra were recorded on an X-ray photoelectron spectrometer (ESCALAB 250Xi) with Al K\\u03b1 radiation (h\\u03bd = 1486.6 eV) as the illumination source. Ultraviolet-visible absorption spectra were recorded using a UV-vis-NIR spectrophotometer (Lambda 950, PerkinElmer, USA) in the 300\\u2013800 nm wavelength range at room temperature. Steady-state and time-resolved PL spectra were detected using a fluorescence spectrometer (FLS920, Edinburgh Instruments, U.K.). The steady-state PL spectra were collected by illuminating the sample with a monochromatic xenon lamp source (\\u03bbexc = 460 nm). The TRPL spectra were acquired with samples photoexcited by a pulsed laser beam (405 nm, 10 MHz, pulse duration of <100 ps) in a time-correlated single photon counting (TCSPC) mode. The photoelectron emission spectra were recorded with an AC-2 instrument (AC-2, RIKEN Instruments, Japan) with a reference sample of Au. The photocurrent\\u2013voltage characteristics of perovskite solar cells were measured using a calibrated (with a standard silicon solar cell) solar simulator (91192, Oriel, USA) with a digital source meter (2400, Keithley Instruments, USA) under AM 1.5G illumination (100 mW cm2), and the active area of the tested solar cells was defined as 0.06 cm2 and 1 cm2 using metal masks. A 450 W xenon lamp (69920, Newport, USA) was used for steady-state power measurements. The IPCE spectra were obtained using a QEX10 solar cell quantum efficiency measurement system (QEX10, PV measurements). Electrochemical impedance spectra (EIS) were recorded using a Zahner system under dark conditions with a bias of \\u22120.9 V, with frequencies ranging from 1 Hz to 1 M Hz and a modulation amplitude of 10 mV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: CsPbBrI2,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150,\\n Perovskite_deposition_thermal_annealing_time: 1,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1200,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 10,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO glass (TEC15, NSG) was washed with soap water, DI-water, ethanol, and isopropanol sequentially. Then, a TiO2 blocking layer (0.15 M titanium diisopropoxide bis-(acetylacetonate) in 1-butanol solution) was deposited on the FTO glass (17 mm \\u00d7 17 mm) at 2000 rpm for 20 s and heated at 125 \\u00b0C for 5 min. The mesoporous TiO2 layer was deposited on the TiO2 blocking layer (bl-TiO2) at 5000 rpm for 30 s and sintered at 550 \\u00b0C for 120 min using a commercial TiO2 paste (Dyesol 30 NRD, Dyesol) diluted by ethanol with a weight ratio of 1:2.5.\\nThe perovskite film was fabricated by a modified two step method. The Pb\\u2013Br precursor films were spin-coated onto mesoporous TiO2 layers at 2000 rpm for 20 s using 1.4 M PbBr2 solution in a mixed solvent of dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) (9:1 volume ratio). The Pb\\u2013Br precursor films were then immediately dipped into 1.7 mg ml\\u22121 CsBr\\u2013isopropanol (IPA) solution (CsBr\\u2013IPA saturated solution) for different reaction times or into 1.7 mg ml\\u22121 CsBr\\u2013methanol solution for 240 s at room temperature. Then, the resulting intermediate films were immersed into 17 mg ml\\u22121 CsBr methanol solution for 5 min at 50 \\u00b0C. The obtained films were washed with IPA, followed by heating at 250 \\u00b0C for 5 min to get CsPbBr3 films.\\nFinally, commercial carbon paste (MTW-CE-C-003, Shanghai MaterWin New Materials Co., Ltd.) was painted on the CsPbBr3 layers, followed by heating at 110 \\u00b0C for 30 min. All the fabrication steps above were conducted in ambient air.\\n\\nSurface and cross-section morphologies were observed using a JSM-7500F field emission scanning electron microscope (FESEM). X-ray diffraction (XRD) patterns were collected with a Rigaku D/MAX-2500 X-ray diffractometer using Cu K\\u03b1 radiation (\\u03bb = 0.1541 nm) with a speed of 6\\u00b0 min\\u22121. Absorption spectra were measured on a UV-3000 ultraviolet and visible (UV-vis) spectrophotometer. The photoluminescence (PL) spectra were obtained on a lifetime and steady state spectrometer (FLS920, Edinburgh Instruments Ltd.) with an excitation wavelength of 515 nm at room temperature. Surface roughnesses were characterized using a Bruker Dimension ICON atomic force microscope (AFM). The optical photographs were taken using a digital camera (Olympus E-PL1, Japan) with BUAA printed on a white background.\\nThe J\\u2013V measurements were recorded on a Zahner photo-electrochemical workstation with the scans (a voltage step of 50 mV and a delay time of 100 ms) performed under the illumination of a solar simulator (Newport SOL3A 94023A, 100 mW cm\\u22122, AM 1.5), and the intensity was calibrated with a certified Si-reference cell (Newport). IPCE spectra were recorded on an IPCE kit (E0201, Institute of Physics, Chinese Academy of Sciences). For the stability test at room temperature (20\\u201330 \\u00b0C), the devices were stored in ambient air (RH \\u223c 25\\u201385%). For the heat stress tests, the devices were stored in an oven (80 \\u00b0C) in dry air (RH \\u223c 10\\u201320%). J\\u2013V curves were measured periodically to obtain the photovoltaic parameters. All of the above characterizations were carried out in ambient air.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: CsPbBr3,\\n Perovskite_composition_short_form: CsPbBr,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Ion exchange,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 250.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 5.0,\\n HTL_stack_sequence: none,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Unknown,\\n Backcontact_stack_sequence: Carbon,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Painting,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 80.0; 80.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: 5.62,\\n Stability_PCE_end_of_experiment: 100,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials were purchased from Sigma-Aldrich and used without further purification.\\n\\nFluorine-doped tin oxide-coated glasses (NSG TEC A7) were sequentially cleaned by ultrasonication using distilled water, acetone, isopropanol, and ethanol for 15 min respectively, and then treated with UV\\u2013ozone for 15 min. A 20\\u201330 nm TiO2 blocking layer was deposited via spray pyrolysis at 450 \\u00b0C using a precursor solution of titanium diisopropoxide bis(acetylacetonate) (75% in 2-propanol) diluted in ethanol (Fisher, Absolute, HPLC grade) (1:10, volume ratio) and oxygen as a carrier gas. To deposit the mesoporous TiO2 layer, TiO2 paste (Dyesol, 30 NRD) was firstly diluted in ethanol with a weight ratio of 1:6, and then spin-coated onto the TiO2 compact layer at a speed of 5000 rpm for 20 s with a ramp-up of 2000 rpm s\\u22121. After spin-coating, the substrate was immediately dried on a hotplate at 100 \\u00b0C and then sintered at 500 \\u00b0C for 30 min. For the Li doping of the TiO2 substrate, 50 \\u03bcL LiTFSI solution in acetonitrile (10 mg mL\\u22121) was spin-coated on the as-fabricated TiO2 substrate at a speed of 3000 rpm with a ramp-up of 2000 rpm s\\u22121 for 10 s, followed by another sintering step at 500 \\u00b0C for 30 min. Thereafter, the substrates were transferred into a N2-filled glove box immediately for further perovskite deposition. For the deposition of the perovskite film, the precursor solution was prepared by mixing FAI (1.0 M), MABr (0.2 M) (Dyesol), PbI2 (1.1 M) (TCI), and PbBr2 (0.2 M) in a mixed solvent of 173 \\u03bcL of DMSO and 692 \\u03bcL of DMF (v/v = 1:4). After stirring for 1 h, 45 \\u03bcL of CsI solution (1.5 M in DMSO) was added to the as-prepared solution. 50 \\u03bcL of the precursor solution was spin-coated in a two-step process at 1000 rpm and 5000 rpm for 10 s and 20 s, respectively. During the second step, 150 \\u03bcL of chlorobenzene was dripped on the spinning substrate at 5 s before the end of the procedure. The as-prepared film was immediately annealed on a hotplate at 100 \\u00b0C for 30 min. After cooling down to room temperature, 50 \\u03bcL of CuSCN solution (20 mg mL\\u22121 in diethyl sulfide) was spin-coated onto the perovskite film at a speed of 5000 rpm for 30 s and then annealed at 50 \\u00b0C for 10 min. The deposition of CuSCN was carried out in a dry air filled glove box with a temperature of 20 \\u00b0C and relative humidity lower than 10%. To deposit the carbon electrode, 5 mg of multi-walled carbon nanotubes or carbon black was dispersed in 1 mL chlorobenzene under ultrasonication, and then deposited on top of CuSCN by a drop-casting method.\\n\\nPhotocurrent density\\u2013voltage (J\\u2013V) curves were measured using a digital source meter (Keithley 2400) under 1 sun conditions (ABET M-SLSS solar simulator), and the light intensity was calibrated using an NREL-calibrated Si solar cell equipped with an infrared cutoff filter (Schott KG-5). A shadow mask with an area of 0.067 cm2 was used for an accurate determination of the device area and short-circuit current density. The IPCE test was performed on an IPCE system (Enli tech, QE-R666) in DC mode, where the monochromatic beam was supplied by a 75 W xenon lamp. SEM images were recorded using a field-emission SEM (Hitachi S-8000 scanning electron microscope). XRD measurements were performed on a D8 Advance diffractometer (Bruker AXS). Ultraviolet visible absorption and steady-state photoluminescence spectra were acquired using a flame spectrometer (Ocean Optics) in a N2-filled glovebox. Time-resolved photoluminescence was measured using a fluorescence lifetime imaging microscope (FLIM, Leca TCS SP8) with a pulsed excitation laser at a wavelength of 405 nm. The surface morphology of CuSCN films spin-coated on glass and the FTO/TiO2/perovskite substrate was studied using a tapping-mode AFM on a Multimode 8 SPM system (Bruker). The resonant frequency and force constant of the cantilever were 70 kHz and 40 N m\\u22121, respectively. The surface roughness and grain size were determined from a scan area of 1 \\u03bcm2 and 5 \\u03bcm2 in AFM images using Nanoscope software. XPS analysis was carried out using the Thermo Scientific Esacalab250 XPS system, with a spot size of 500 \\u03bcm, pass energy of 20 eV, and energy steps of 0.05 eV.\\n\\nFor the moisture stability test of C-PSCs, unencapsulated devices were stored in a lab with a relative humidity of 85 \\u00b1 10% at room temperature, and then J\\u2013V curves were measured every 20 hours. To conduct the photostability test, some unencapsulated devices were placed in an unclosed chamber, which was purged with continuous N2 flow. Then the devices were exposed to a LED light source with a power density of 100 mW cm\\u22122, no cooling system was adopted to control the device temperature, and J\\u2013V curves were measured every 100 hours.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | Li-TFSI,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.81MA0.14PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: CuSCN,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Carbon-nt,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Dropcasting,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: 17.58,\\n Stability_PCE_end_of_experiment: 80,\\n Cell_area_measured: 0.067,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals are of analytical grade and applied directly without any purification. PbI2 (99.999%), CH3NH3I and Spiro-OMeTAD (\\u226599%) were purchased from Xi'an Polymer Light Technology Co., Ltd. (China). DMF (99.8%), DMSO (\\u226599%), anhydrous acetonitrile (99.8%), 4-tert-butylpyridine (TBP, 96%), bis(trifluoromethane)sulfonamide lithium salt (Li-TFSI, 99.95%) and chlorobenzene (99.5%) were purchased from Sigma-Aldrich.\\n\\nFluorine doped tin oxide (F:SnO2) coated glass (FTO) was patterned by etching with 2 M HCl and Zn powder. The patterned FTO was cleaned by ultra-sonication and rinsed with detergent, deionized water, ethanol, acetone and isopropanol for 30 min, respectively. Then, the FTO was dried using clean air and treated with a UV-ozone machine for 15 min. The TiO2 compact layer was prepared by spin-coating a precursor solution of 0.15 M titanium diisopropoxide bis(acetylacetonate) (75 wt% in isopropanol, Alfa-Aesar) in 1-butanol (99.9%, Alfa-Aesar). After spin-coating, the substrates were annealed at 550 \\u00b0C for 30 min and then they were left to cool down to room temperature.\\n\\nA solution of 1 M PbI2/1 M MAI was dissolved in a DMSO solvent and the solution was stirred at 60 \\u00b0C for 30 min before spin coating. The prepared solution was then spin-coated onto the compact TiO2/FTO glass substrates at a speed of 4000 rpm for 30 s. Chlorobenzene (CB, 100 \\u03bcL) was added dropwise on the spinning substrates at 15 s before the end of the spin coating procedure. Then, the obtained MAPbI3 precursor films were annealed under different conditions. For the conventional annealing (CA) route, the substrate was placed on the hot plate in contact with glass side. For the conductive glass (FTO)-assisted annealing method, called the novel annealing (NA) route, the surface of the MAPbI3 precursor films is in contact with the FTO directly. It should be noted that the surface of the FTO needed to be cleaned and preheated to 100 \\u00b0C before the perovskite film annealing. Briefly, the different novel annealing times of 15, 30 and 60 min were denoted as NA-15, NA-30 and NA-60, respectively.\\n\\nAfter the perovskite annealing, the substrate was cooled down for a few of minutes. The hole transport material (HTM) was spin-coated onto the perovskite film at 4000 rpm for 20 s. An HTM solution was prepared by dissolving 72.3 mg of (2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene) (Spiro-MeOTAD) in 1.0 mL of chlorobenzene, into which 28.8 \\u03bcL of 4-tert-butylpyridine and 17.5 \\u03bcL of Li-TFSI solution (520 mg Li-TFSI in 1 mL acetonitrile) were added. Finally, a gold electrode with a thickness of 80 nm was thermally evaporated on top of the device to finish the fabrication. The active area of the small area device was 0.09 cm2 and that of the large area device was 1 cm .\\n\\nThe photovoltaic performance of PSCs was recorded using a source meter (Keithley 2400). A PEC-L11 AM 1.5 solar simulator with a 1000 W Xe lamp and an AM 1.5 filter (Peccell) was used as the light source (100 mW cm\\u22122). J\\u2013V curves were measured at a scan rate of 20 mV s\\u22121. The incident photon-to-current conversion efficiency (IPCE) spectra were collected using a PEC-S20 (Peccell). Electrochemical impedance spectroscopy (EIS) was conducted using an IM6 (Zahner). The impedance parameters were simulated by fitting the impedance spectrum through the Z-view software.\\nThe phase purity of the samples was characterized by powder X-ray diffraction (XRD) on a Rigaku Ultima IV using Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5). The crystalline morphologies were examined by scanning electron microscopy (Hitachi S-4800 instrument). Atomic force microscopy (AFM) measurements were obtained using a SPA-300 AFM (Bruker) and the scanning range of the AFM images was 5 \\u03bcm \\u00d7 5 \\u03bcm. Steady-state photoluminescence (PL) (excitation at 406 nm) and time-resolved photoluminescence (TR-PL) (excitation at 406 nm and emission at 750 nm) were conducted using an FLS 980 (Edinburgh Instruments LTD). The contact angles were measured on a OCA20 machine. The absorption spectra were measured using a UV-vis spectrophotometer (Perkin-Elmer, Lambda 950).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 120,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 51,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (CH3NH3I), PEDOT:PSS (Clevious P VP AI 4083), SnI2 (99.999%), PCBM (99.9%), PEI(99.9%), and Al (99.99%) were purchased from H. C. Stark Company, Alfa Aesar, Puyang Yongxin Fullerene Technology Co., Ltd, Xi'an Polymer Light Technology Corp, sigma and China New Metal, respectively. The ITO-coated glass substrates were cleaned successively with detergent, deionized water, and isopropyl alcohol in an ultrasonic bath for 30 min, respectively, and then treated with oxygen plasma for 15 min. PEDOT:PSS aqueous solution was filtered through a 0.45 \\u03bcm filter and spin coated on the ITO surface at 3000 rpm for 40 s and then annealed at 140 \\u00b0C for 15 min, forming a hole transport layer. The perovskite films without Pb(SCN)2 in the precursors were prepared by spin coating the precursor solutions consisting of 186.3 mg of SnI2 and 79.5 mg of MAI dissolved in 464 \\u03bcL of N,N-dimethylformamide and 36 \\u03bcL of dimethyl sulfoxide. The molar ratio between SnI2 and MAI is 1:1. The perovskite films with 5%, 10%, 15%, 20%, 25% and 30% Pb(SCN)2 (Sigma, 99.5%) in the precursors were prepared by spin coating the solutions with Pb(SCN)2. All the perovskite precursors with and without Pb(SCN)2 were stored at 70 \\u00b0C and stirred overnight in a glove box. The following procedures for the fabrication of the solar cells were performed in a nitrogen-purged glove box. A PEDOT:PSS layer was then spin-coated onto the ITO substrates at 4000 rpm for 60 s and dried at 140 \\u00b0C for 20 min. The coated substrates were then transferred to a nitrogen-filled glove-box. The perovskite layer was spin-coated on the PEDOT:PSS substrate at 5000 rpm for 20 s. The mixed solvent of toluene:chloroform (7:3 in volume) was used as the antisolvent during the spin-coating process. Then the perovskite film was placed in a vacuum cover and a mechanical pump was employed to keep the working pressure inside the cover at 1.325 kPa. After 10 minutes the perovskite film was annealed at 100 \\u00b0C for 10 minutes in the vacuum cover. After the fabrication of perovskite layer, PCBM was spin-cast at 2000 rpm for 60 s from a 20 mg mL\\u22121 chlorobenzene solution. Then PEI was spin-cast at 3000 rpm for 60 s from a 0.1 wt% isopropanol. Finally, Al (90 nm) was deposited through a mask via thermal evaporation at a rate of 0.2\\u20131.0 \\u00c5 s\\u22121 to produce 0.045 cm2 pixels.\\n\\nThe XRD patterns were detected with a Bruker D8 Advance X-ray diffraction meter. The absorption spectra of the photoactive perovskite films coated on the ITO substrates were measured by an ultraviolet visible (UV-Vis) absorption spectrophotometer (Shimadzu UV-3101PC). The morphologies and the elemental mappings energy dispersive spectrometer (EM-EDS) of the perovskite films were investigated using a scanning electron microscope (SEM, Hitachi S-4800) with an accelerating voltage of 15 kV. The photoluminescence (PL) spectra of the perovskite films were measured by a fluorescence spectrophotometer. Fourier Transform Infrared (TRPL) spectra were performed by a square-pulsed optical excitation which was generated from a light emitting diode (LED) driven by a function generator, and a 50 \\u03a9 input termination of the oscilloscope was used. The current density\\u2013voltage (J\\u2013V) curves of the inverted PSCs were measured by a Keithley 6430 Source Measure Unit under nitrogen and a Mass 1.5 G illumination at 100 mW cm\\u22121\\u22122 (SAN-EI Electric, XEC-301S). The incident photon-to-current efficiency (IPCE) was performed using a solar cell QE/IPCE measurement system (Zolix Solar Cell Scan 100). The light intensity dependent photo voltage (LIPV) was conducted using an array of 12 focused cool white LEDs of 1 W. The stability test was carried out in air with 50% humidity. The light intensity of the LEDs was detected by a corrected Si photodiode, and the electrical input power of the LEDs was adjusted with a controlled power supply to change the illumination intensities ranging from 5 to 500 mW cm\\u22122. The values of the open-circuit voltage (Voc) and the short-circuit current density (Jsc) were collected by a 16 bit data acquisition board (NI-6052E) with an input impedance of 10 M\\u03a9 and 50 \\u03a9 at room temperature, respectively. In order to reach a steady-state condition, the time of the data acquisition was chosen to be 100 ms through the measurement process. The transient photocurrent (TPC) measurement was conducted using a signal generator with a voltage signal of 200 \\u03bcs and 50 Hz as a power supply of the white LEDs that produced pulsed light. The device was connected with a resistor of 50 \\u03a9 in series and the voltage applied to the resistor was collected by the oscilloscope and the TPC was calculated simply by the voltage divided by the resistance.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PEI,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MASnI3,\\n Perovskite_composition_short_form: MASnI,\\n Perovskite_additives_compounds: Pb(SCN)2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1.83,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 50,\\n Cell_area_measured: 0.045,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The FASnI3 precursor solution was prepared by dissolving 372 mg of SnI2, 172 mg of formamidinium iodide (FAI) and 15.6 mg of SnF2 in 1 mL of mixed solvent of N,N-dimethylmethanamide (DMF) and dimethyl sulfoxide (DMSO), where the ratio of DMF:DMSO was 4:1. The MAPbI3 precursor solution was prepared by dissolving 461 mg of PbI2 and 159 mg of methylammonium iodide (MAI) in 0.7 mL of the aforementioned mixed solvent. The FA0.5MA0.5Sn0.5Pb0.5I3 precursor solution was obtained by mixing stoichiometrically identical amounts of FASnI3 and MAPbI3 precursor solutions, followed by stirring for 12 hours.\\n\\nITO glass substrates were sequentially washed with isopropanol, acetone, distilled water and isopropanol, then dried in an oven. For device fabrication, ITO glass was treated by plasma treatment, followed by the deposition of 10 nm-thick ZnO nanoparticles (purchased from Sigma Aldrich) through spin-coating. Subsequently, 40 nm-thick SnO2 nanoparticles (purchased from Alfa Aesar) were spin-coated on the ITO/ZnO substrate, followed by annealing at 150 \\u00b0C for 30 min. For SnO2 modification, C60-SAM solution (1.5 mg mL\\u22121 in chlorobenzene) was spin-coated above the SnO2 layer at a spin speed of 4000 rpm for 30 s, and then spin-treated with chlorobenzene to wash away the residual C60-SAM. From the X-ray photoelectron spectroscopy (XPS) and atomic force microscope (AFM) measurements shown in Fig. S1 (ESI\\u2020), we confirmed the existence of C60-SAM above the SnO2 layer via the appearance of the N 1s signal, and observed that the C60-SAM-deposition process had no influence on the SnO2 morphology. Finally, the FA0.5MA0.5Sn0.5Pb0.5I3 precursor solution was spin-coated above the ITO/ZnO/SnO2/C60-SAM layer to form a 500 nm-thick perovskite film, followed by the deposition of a 40 nm-thick poly(3-hexylthiophene-2,5-diyl) (P3HT) layer, 10 nm-thick MoO3 layer and 100 nm-thick Ag electrode.\\n\\nUltraviolet-visible light absorption spectra were recorded on an HP8453 spectrophotometer. Scanning electron microscope (SEM) images were obtained by a Zeiss EVO 18 SEM. The crystalline structure of the perovskite films was investigated by an X-ray diffractometer (PANalytical X\\u2019pert PRO) equipped with a Cu-K\\u03b1 X-ray tube. The XPS data were obtained by using ESCALAB 250Xi equipment. Ultraviolet photoelectron spectroscopy (UPS) data were obtained using a K-ALPHA+ instrument. AFM images were obtained by a Bruker Multimode 8 scanning probe microscope.\\n\\nThe current density\\u2013voltage (J\\u2013V) characteristics for the devices were measured under conditions of 100 mW cm\\u22122 air mass, 1.5 global (AM 1.5G) illumination with a solar simulator (Taiwan, Enlitech, SS-F5). The light intensity was calibrated with a National Renewable Energy Laboratory-calibrated silicon photodiode using a KG5 filter. The external quantum efficiency (EQE) of the devices was measured on a commercial QE measurement system (QE-R3011, Enlitech). For the transient photovoltage (TPV) measurements, the device was serially connected to a digital oscilloscope (Tektronix TDS 3052C), and the oscilloscope's input impedance was set to 1 M\\u03a9 to form open-circuit conditions. The TPV was measured under 0.3 sun illumination. An attenuated laser pulse (0.54 \\u03bcJ cm\\u22122; 530 nm) was used as a small perturbation to the device's background illumination. The laser pulses were generated from an optical parametric amplifier (TOPAS-Prime) pumped by a mode-locked Ti:sapphire oscillator-seeded regenerative amplifier, with a pulse energy of 1.3 mJ at 800 nm and a repetition rate of 1 kHz (SpectraPhysics Spitfire Ace). The time resolution of the overall measurement was approximately 1 ns. The light-dependent Voc measurements were performed under the J\\u2013V measurement system, and the light intensity was modulated from 0.1 sun to 1 sun. The transient photocurrent (TPC) and electrochemical impedance spectroscopy (EIS) measurements were carried out using a Paios 4.0 Measurement Instrument (FLUXiM AG, Switzerland).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np | C60-SAM,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.5MA0.5Pb0.5Sn0.5I3,\\n Perovskite_composition_short_form: FAMAPbSnI,\\n Perovskite_additives_compounds: SnF2,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 750,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 84,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"MAPbI3-0P, MAPbI3-0.5P, MAPbI3-1P, and MAPbI3-10P OIHP thin films were prepared by the (anti)solvent-assisted one-step spin-coating method. A base MAPbI3-0P precursor solution of 40 wt % concentration was prepared by co-dissolving 0.461\\u00a0g of PbI2 (99.9985%, Alfa Aesar, USA) and 0.159\\u00a0g of MAI (Dyesol, Australia) in 0.930\\u00a0g of DMF (Sigma-Aldrich, USA) solvent. For the preparation of MAPbI3-0.5P, MAPbI3-1P, and MAPbI3-10P solutions, 0.003, 0.006, and 0.031\\u00a0g of Pluronic P123 was added, respectively. Subsequently, the precursor solutions were spin-coated at 4,000\\u00a0rpm for 30\\u00a0s on appropriate substrates. At 7\\u00a0s after the start of the spin-coating step, 0.6\\u00a0mL of chlorobenzene was quickly dripped. The spin-coated thin films were then annealed at 130\\u00b0C for 5\\u00a0min.\\n\\nXRD patterns were obtained under Cu K\\u03b1 radiation (\\u03bb\\u00a0= 0.15406\\u00a0nm) with a step size of 0.02\\u00b0 on an X-ray diffractometer (Bruker D8-advance, Karlsruhe, Germany). The surface morphology of the thin films was characterized by SEM (LEO 1530VP, Carl Zeiss, Germany). The local roughness of the thin films was characterized by AFM (MFP-3D Origin, Asylum Research, USA) with a silicon probe. Conductive AFM measurements were made with the same instrument in contact mode with a conducting platinum-coated silicon probe (Econo-SCM-PIC, Asylum Research, USA). UV-vis spectra were obtained with a spectrophotometer (UV-2600, Shimadzu, Japan) equipped with an integrating sphere attachment (ISR-2600, Shimadzu, Japan). A standard BaSO4 pellet (Nacalai Tesque, Japan) was used as the reference. UV-vis spectra of the solutions were obtained with the same spectrophotometer without the integrating sphere attachment. FTIR spectra were obtained on a spectrometer (4100, Jasco Instruments, USA). Samples for the FTIR measurements were prepared by scratching the thin films from the substrates.\\n\\nAtomistic simulations at the DFT level were performed with CP2K 3.0 code and the hybrid Gaussian and plane-wave method implemented in the Quickstep module. The Perdew-Burke-Ernzerhof functional with Grimme correction was adopted to describe the dispersion interactions. A mixed Gaussian basis set (DZVP-MOLOPT) and norm-conserving GTH pseudopotentials were used on all atoms. The binding energy (E Binding) is defined by E Binding\\u00a0= E Perovskite\\u00a0+ E P123 \\u2013 E Perovskite-P123, where E Perovskite, E P123, and E Perovskite-P123 are the energies of MAPbI3, P123, and the whole system (shown in Figure\\u00a01C), respectively.\\n\\nFTO-coated glass substrates were patterned by etching with Zn powder and 1\\u00a0M HCl diluted in distilled water. The etched substrates were first soaked in a saturated KOH ethanol solution for 12\\u00a0hr and cleaned sequentially with deionized water and ethanol. The substrates were then blow-dried with N2 gas and were further subjected to UV light. Compact TiO2 films on the FTO substrates were obtained by spray pyrolysis at 450\\u00b0C. After cooling down to room temperature, the substrates were then transferred into a N2-filled glovebox for deposition of the MAPbI3-0P, MAPbI3-0.5P, MAPbI3-1P, or MAPbI3-10P OIHP thin films according to the above procedure. A hole-transporting material solution was spin-coated on the OIHP films at 4,000\\u00a0rpm for 30 s; this was prepared by dissolving 80\\u00a0mg of 2,2\\u2032,7,7\\u2032-tetrakis (N,N-di-methoxyphenylamine)-9,9\\u2032-spirobifluorene (Spiro-OMETAD, Merck, Germany), 28.8\\u00a0mL of 4-tert-butylpyridine, and 17.5\\u00a0mL of lithium bis (trifluoromethylsulfonyl) imide (Li-TFSI) solution (520\\u00a0mg Li-TFSI in 1\\u00a0mL acetonitrile) in 1\\u00a0mL of chlorobenzene. Finally, Au electrode was deposited by thermal evaporation to complete the device. The champion PSC was made by optimization of the above fabrication procedures and details with the MAPbI3-0.5P thin film. The EQE spectra were obtained in AC mode with a solar cell quantum efficiency measurement system (EQE-200, Oriel Instruments, USA). The J-V characteristics of the PSCs were measured with a 2400 Sourcemeter (Keithley, USA) under simulated 1-sun AM 1.5G 100 mW cm\\u22122 intensity (Oriel Sol3A Class AAA, Newport, USA) in both reverse (from V OC to J SC) and forward (from J SC to V OC) scans. The step voltage was 25\\u00a0mV with 5\\u00a0ms of delay time per step. A typical active area of 0.12\\u00a0cm2 was defined with a non-reflective mask for the J-V measurements.\\n\\nThe PSCs were placed in a sealed holder with a transparent glass cover. A flow of Ar gas was continuously passed through the holder to minimize the water and oxygen content in the atmosphere. J-V curves were performed every 2\\u00a0hr. The temperature of the PSCs was maintained at \\u223c40\\u00b0C under continuous 1-sun illumination. Between the J-V measurements, the PSCs were biased at the maximum-power-point voltage with a potentiostat under illumination.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 130,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 40.0; 40.0,\\n Stability_atmosphere: Ar,\\n Stability_time_total_exposure: 480,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A fluorine-doped tin oxide glass (FTO, TEC8, Pilkington) substrate was washed by sonication in ethanol, acetone, and isopropanol for 20\\u202fmin. After UV-ozone treatment for 20\\u202fmin, a compact (c)-TiO2 layer was deposited on the FTO substrate by spin coating a diluted titanium diisopropoxide bis(acetylacetonate) solution (75% in isopropanol, Aldrich) with 1-butanol at 2000\\u202frpm for 40\\u202fs followed by heating at 500\\u202f\\u00b0C for 30\\u202fmin. The solution for the mesoporous (mp)-TiO2 layer was prepared by diluting a lab-made TiO2 paste [] with anhydrous ethanol (1:3.5\\u202fwt ratio). The mp-TiO2 layer was coated onto the c-TiO2 layer by spin coating the diluted TiO2 paste solution at a spin rate of 3500\\u202frpm for 40s and then annealing at 500\\u202f\\u00b0C for 30\\u202fmin. A MAPbI3 perovskite solution was prepared by dissolving 1.4\\u202fM PbI2 (99.9985%, Alfa Aesar) and 1.4\\u202fM CH3NH3I (Greatcell Solar) in 1\\u202fmL of N,N-dimethylformamide (DMF, 99.8%, Alfa Aesar) and dimethyl sulfoxide (DMSO, 99.9%, Aldrich) mixed solvent (9:1, v/v). The MAPbI3 layer was prepared by spin-coating the perovskite solution at 1000\\u202frpm for 5\\u202fs and then 4000\\u202frpm for 15\\u202fs onto the ETLs. During spin-coating, diethyl ether was dropped onto the rotating film 7\\u202fs before the end of the coating process and the film was heated on a hot plate at 65\\u202f\\u00b0C for 1\\u202fmin and then at 100\\u202f\\u00b0C for 10\\u202fmin. The Spiro-OMeTAD solution was prepared by dissolving 56\\u202fmg of Spiro-OMeTAD (Merck), 30\\u202fmg of 4-tert-butylpyridine (tBP, 96%, Aldrich), and 6\\u202fmg of lithium-bis(trifluoromethanesulfonyl) imide (LiTFSI, 99.95%, Aldrich) in 1\\u202fmL of chlorobenzene (99.8%, Aldrich). The Spiro-OMeTAD solution was then spin-coated at 2500\\u202frpm for 20\\u202fs. For the polymeric HTLs, an FEH or P3HT solution was prepared by dissolving 15\\u202fmg of the polymer in 1\\u202fmL chlorobenzene. Then, 5\\u202f\\u03bcL of a LiTFSI stock solution (520\\u202fmg in 1\\u202fmL acetonitrile) and 15.2\\u202f\\u03bcL of tBP were added to the solution. The polymer solution was coated onto the perovskite layer at a spin-rate of 3000\\u202frpm for 30\\u202fs. Finally, an 80\\u202fnm-thick Au electrode was deposited on top of the device by thermal evaporation.\\n\\nThe number of average molecular weights (M n) and polydispersity index (PDI) of polymers were obtained by measuring gel permeation chromatography (Waters, refractive index detector Waters 2414) eluted with chlorobenzene as an eluent (P3HT: M n\\u202f=\\u202f52\\u202fkDa, PDI\\u202f=\\u202f2.8; FEH: M n\\u202f=\\u202f14\\u202fkDa, PDI\\u202f=\\u202f2.13). The surface morphology of the HTLs and cross-sectional images of the devices were obtained by atomic force microscopy (AFM, XE-100, Park Systems) and field-emission scanning electron microscopy (FESEM, Inspect F, FEI). Ultraviolet photoelectron spectroscopy (UPS) measurements were performed with a scanning XPS microprobe (PHI 5000 VersaProbe, Ulvac-PHI) using HeI (21.2\\u202feV). The UV-Vis absorbance spectra of the HTLs were obtained using a UV-Vis spectrometer (Lambda 35, PerkinElmer). The space charge limited current (SCLC) current-voltage (J\\u2013V) curves were measured using hole-only devices (ITO/PEDOT:PSS/HTL material/Au) under dark conditions. The SCLC hole mobilities of the HTL materials were obtained using the Mott-Gurney square law, J = (9/8) \\u03b5 0 \\u03b5 r \\u03bc (V 2/L 3), where \\u03b5 0 is vacuum permittivity, \\u03b5 r is the dielectric constant of the HTL material, \\u03bc is the charge carrier mobility, V is the effective applied voltage, and L is the thickness of the film. Steady-state photoluminescence (PL) spectra were measured using a Fluorolog3 PL spectrometer system with a monochromator (iHR320, HORIBA Scientific) excited at 530\\u202fnm. Fluorescence-lifetime imaging microscopy (FLIM) was performed using an inverted-type scanning confocal microscope (MicroTime-200, Picoquant, Germany). As an excitation source, a single-mode 470-nm pulsed diode laser with a pulse width of \\u2248100 ps and an average power of <0.1\\u202f\\u03bcW was used. A dichroic mirror (490 DCXR, AHF), a long-pass filter (HQ500lp, AHF), and a single photon avalanche diode (PDM series, MPD) were used to measure emissions from the samples, and time-correlated single-photon counting (TCSPC) was used to count the fluorescence photons. Current density-voltage curves were recorded using a Keithley 2400 source measurement unit and a solar simulator equipped with a 180\\u202fW xenon lamp (Yamashida Denso, YSS-50A). A National Renewable Energy Laboratory-calibrated Si solar cell equipped with a KG-3 filter was used to adjust a light intensity to solar conditions (AM 1.5G and 100\\u202fmW\\u202fcm\\u22122). The active area of each cell was measured using an optical microscope camera (Moticam 1000). External quantum efficiencies (EQE) were obtained using a K3100 spectral EQE measurement system (McScience, Inc.).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65; 100,\\n Perovskite_deposition_thermal_annealing_time: 1.0; 10.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 500,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped SnO2 (FTO) coated glass substrates were successively cleaned with deionized water, acetone, isopropanol and ethanol by sonication for 20\\u202fmin, then dried with nitrogen (N2) flow. Oxygen UV treatments were subsequently applied to the FTO substrates for 15\\u202fmin, then the cleaned FTO substrates were immersed in a 0.2\\u202fM aqueous solution of titanium chloride (TiCl4, 99.6%, Alfa Aesar) or gallium nitrate hydrate (Ga(NO3)3\\u00b7xH2O, 99.99%, Aladdin)/titanium chloride (molar ratios: 3%, 5%, 7%, 9%) in a closed vessel at 70\\u202f\\u00b0C for 55min. The deposited substrates were washed with deionized water several times to remove loosely bound materials, dried with N2 flow and annealed at 200\\u202f\\u00b0C for 30\\u202fmin in air.\\n\\nThe 40\\u202fwt% perovskite precursor solution was prepared by dissolving CH3NH3I (synthesized according to previous report[]) and PbCl2 (99.99%, Aladdin) of a 3:1\\u202fM ratio in anhydrous N, N-dimethylformamide (DMF, 99.8%, Sigma-Aldrich) at 60\\u202f\\u00b0C. After TiO2/FTO or Ga-TiO2/FTO substrates being treated by Oxygen UV for 10\\u202fmin, perovskite precursor solution was spin-coated on them at a speed of 3000\\u202frpm for 30\\u202fs in the glove box. All the samples were then heated on a hot plate at 100\\u202f\\u00b0C for 60\\u202fmin, the dark perovskite films can be formed. Subsequently, a thin layer of Spiro-OMeTAD was deposited on the perovskite layer by spin-coating a chlorobenzene solution containing 80\\u202fmM Spiro-OMeTAD, 64\\u202fmM 4-tert-butylpyridine (TBP, Aladdin) and 24\\u202fmM Li-bis (trifluoromethylsulfonyl) imide lithium salt (Li-TFSI, Sigma-Aldrich) (520\\u202fmg/ml in acetonitrile) at 4000\\u202frpm for 30\\u202fs. Finally, silver (Ag) electrode with the thickness of \\u223c100\\u202fnm was evaporated as top electrode via thermal evaporation through a shadow mask. The active area of these devices was 0.045\\u202fcm2.\\n\\nThe Cyclic voltammetry (C-V) measurement was carried out in an electrochemical workstation with aqueous solution of Fe(CN)6 3\\u2212/4- as electrolyte. X-ray photoelectron spectroscopy (XPS) was measured by using AL K-Alpha X-ray photoelectron spectrometer (Thermo Fisher Scientific, UK). The percentages of Ti and Ga in the film are checked by inductively coupled plasma mass spectrometry (ICP-MS, SPECTRO ARCOS MV). The current density-voltage (J-V) characteristics of PSCs, FTO/TiO2/Ag and FTO/Ga-TiO2/Ag were performed by Keithley 2400 source meter under an illumination of 100\\u202fmW/cm2 (Newport 91160, 150\\u202fW solar simulator equipped with an AM 1.5\\u202fG filter). The thickness of ETLs was performed by a profilometer (Dektak XT). The surface morphology of the TiO2, Ga-TiO2 and perovskite films was characterized by scanning electron microscopy (SEM, ZEISS ULTRA 55). Atomic force microscopy (AFM, Asylum Research, Cypher) was employed to investigate the surface potentials and conductivity of TiO2 and Ga-TiO2 films. The external quantum efficiency (EQE) was measured by a standard EQE system (Newport 66902). EIS measurements were performed on a LED (\\u03bb\\u202f=\\u202f526\\u202fnm) with 300\\u202fW/m2 as a light source with an AC amplitude of 20\\u202fmV from 1\\u202fHz to 1\\u202fMHz by the Zahner Zennium electrochemical workstation. The stable photoluminescence spectra (PL) was recorded by a fluorescence spectrophotometer (HITACHI F-5000), which had been normalized to the absorbance and measured in the same conditions. For PL measurement, the excitation wavelength is 515\\u202fnm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 672,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.045,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"1,3-Propanediammonium iodide salt (PDA)I2 was prepared by taking 1 mole equivalent of 1,3-propanediamine (2.6\\u00a0mL) followed by dropwise adding 2 mole equivalents solution of hydroiodic acid (8\\u00a0mL) with continuous stirring at 0\\u00b0C for 2\\u00a0hr. Using a rotary evaporator, the white precipitate of diammonium iodide salt was recovered by evaporation of the solvent at 55\\u00b0C. The precipitate was washed with ethanol and diethyl ether three times. The white powder was collected by suction filtration and dried overnight in an oven at 60\\u00b0C under reduced pressure. The propylammonium iodide (PAI) salt was synthesized following an identical procedure for (PDA)I2, except for the use of 1 mole equivalent of propylamine (5\\u00a0mL) and 1 mole equivalent solution of hydroiodic acid (8\\u00a0mL). The preparation of the DJ phase 2D perovskite precursor solution is described in the Supplemental Information.\\n\\nThe devices were fabricated on 2-mm-thick FTO-coated glasses. The substrates were sequentially cleaned by ultrasonication in ethanol, isopropanol, and acetone each for 30\\u00a0min and finally dried under an N2 flow. Then the substrates were treated in a UV-ozone cleaner for 15\\u00a0min.\\n\\nThe treated substrates were immersed in a 0.2\\u00a0M aqueous solution of TiCl4 and placed in oven at 70\\u00b0C for 1\\u00a0hr. The glass/FTO/TiO2 substrates were then washed with deionized water three times and finally treated with a steam of N2. Before further use, the TiO2 thin film was annealed at 200\\u00b0C for 1\\u00a0hr in air.\\n\\nThe precursor solutions of DJ phase 2D perovskites (PDA) (MA)n-1PbnI3n+1 (n\\u00a0= 1\\u20134) were synthesized from a stoichiometric ratio of MAI, PbI2, and (PDA)I2 in 1\\u00a0mL mixed solvent of \\u03b3-butyrolactone and DMSO (7:3 volume) with various concentrations based on PbI2. The RP phase 2D perovskite (PA)2(MA)3Pb4I13 solution was prepared from a stoichiometric ratio of MAI, PbI2, and PAI. Synthetic procedures in details for each n value are given in the Supplemental Information. The 2D perovskite layers were prepared using a hot-casting method. On the substrate of glass/FTO/TiO2 heated at a specific temperature, a 70\\u00a0\\u03bcL precursor solution was dropped then spin-coated at 4,000\\u00a0rpm for 40 s. The color of the thin film quickly changed from pale yellow to orange yellow for n\\u00a0= 1, to red for n\\u00a0= 2, to dark red for n\\u00a0= 3, and to black for n\\u00a0= 4, during the evaporation of solvent. For all n values and PA-based perovskite layer, the same conditions were applied.\\n\\nThe substrate of the glass/FTO/TiO2/2D perovskite was cooled to room temperature after spin coating of the 2D perovskite layer. The spiro-OMeTAD solution was spin-coated on the perovskite layer at 4,000\\u00a0rpm for 30 s. The spiro-OMeTAD solution was prepared by dissolving 90\\u00a0mg of spiro-OMeTAD in 1\\u00a0mL chlorobenzene with 22\\u00a0\\u03bcL Li-TFSI salt in acetonitrile (520\\u00a0mg/mL) and 36\\u00a0\\u03bcL tBP.\\n\\nA 100-nm-thick counter gold electrode was thermally evaporated under a vacuum of 4\\u00a0\\u00d7 10\\u22124 torr.\\n\\nThe J\\u2212V measurement was performed via a solar simulator (SS-F5-3A, Enlitech) along with AM 1.5G spectra, the intensity of which was calibrated by a certified standard silicon solar cell (SRC-2020, Enlitech) at 100\\u00a0mV/cm2 under ambient conditions. A black metal mask with an aperture was used to control the light scattering and focus the light on the active device area (0.066\\u00a0cm2) during measurement. The EQE data were obtained using a solar-cell spectral-response measurement system (QE-R, Enlitech).\\n\\n\\nThe humidity test of bare devices and thin films was conducted under ambient conditions, where the relative humidity was in the range of 40%\\u201370%. The heat test of both films and unencapsulated devices was carried out under two conditions: (1) placing the samples on a hot plate at 85\\u00b0C in air under 40%\\u201370% RH; (2) the devices were stored inside an environmental chamber at constant temperature and humidity of 85\\u00b0C and 85%, respectively. The light stability test of devices was conducted inside the glove box under constant 1-sun illumination without any encapsulation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Hydrothermal,\\n Perovskite_composition_long_form: MA3PA2Pb4I13,\\n Perovskite_composition_short_form: MAPAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 4000,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 25,\\n Cell_area_measured: 0.066,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless stated otherwise, solvents and chemicals were obtained commercially and\\u00a0used without further purification. N, N-dimethylformamide (DMF), DMSO, chlorobenzene (CB), caffeine, toluene, water, and Ag were obtained from Sigma-Aldrich\\u00a0Inc. TPFB and PbI2 were obtained from TCI Inc. MAI was obtained from\\u00a0One Materials. PTAA was obtained from Xi'an Polymer Light Technology Corp and Sigma-Aldrich Inc (Lot# MKCD5161). Tin oxide (SnO2) nanoparticle was obtained from Alfa-Aesar Inc.\\n\\nPVSK solar cells were fabricated with the following structures: indium tin oxide (ITO), SnO2, MAPbI3, PTAA, and Ag. The ITO glass was pre-cleaned in an ultrasonic bath of acetone and isopropanol, and treated in ultraviolet-ozone for 20\\u00a0min. A thin layer (\\u223c30\\u00a0nm) of SnO2 was spin-coated onto the ITO glass and baked at 150\\u00b0C for 30\\u00a0min. SnO2 was diluted in water (1.67\\u00a0mg mL\\u22121). After cooling at room temperature, the glass, ITO, and SnO2 substrates were transferred into a nitrogen glove box. PVSK solution was prepared by dissolving 159\\u00a0mg MAI and 461\\u00a0mg PbI2 and 71\\u00a0\\u03bcL DMSO in 600\\u00a0\\u03bcL DMF. For the optimized caffeine containing PVSK, 6\\u00a0mg caffeine was added into the solution. The PVSK solution was spin-coated on the substrate at 2,500\\u00a0rpm for 25 s, to which 0.1\\u00a0mL of CB was dropped after 10 s. The spin-coated film was heat treated at 65\\u00b0C for 1\\u00a0min followed by 100\\u00b0C for 20\\u00a0min. The PTAA solution (30\\u00a0mg mL\\u22121, in CB with 10% TPFB) was spun onto the PVSK film as a hole conductor. The devices were completed by evaporating 100\\u00a0nm Ag in a vacuum chamber (base pressure, 5\\u00a0\\u00d7 10\\u22124 Pa).\\n\\nFor MAI\\u00b7PbI2\\u00b7DMSO and MAI\\u00b7PbI2\\u00b7DMSO\\u00b7caffeine adducts,1\\u00a0mmol of PbI2, MAI, and DMSO with or without 6\\u00a0mg caffeine were dissolved in 600\\u00a0\\u03bcL of DMF, to which 10\\u00a0mL of diethyl ether was added to precipitate the corresponding adduct. The precipitates were collected and dried under vacuum.\\n\\nJ-V characteristics of photovoltaic cells were taken using a Keithley 2400 source measure unit under a simulated AM 1.5G spectrum, with an Oriel 9600 solar simulator. Typically, the devices were measured in reverse scan (1.2\\u00a0V \\u2192 0 V, step 0.02 V, 100\\u00a0mV/s) and forward scan (0\\u00a0V \\u2192 1.2 V, step 0.02 V, 100\\u00a0mV/s). All the devices were measured without pre-conditioning such as light-soaking and applied bias voltage. Steady-state power conversion efficiency was calculated by measuring stabilized photocurrent density under constant bias voltage. EQEs were measured using an integrated system (Enlitech, Taiwan) and a lock-in amplifier with a current preamplifier under short-circuit conditions. For TPV and current (TPC) measurements, a white light bias was generated from an array of diodes (Molex 180081-4320) to simulate 0.5 sun bias light working condition. A pulsed red dye laser (Rhodamine 6G, 590\\u00a0nm) pumped by a nitrogen laser (LSI VSL-337ND-S) was used as the perturbation source, with a pulse width of 4\\u00a0ns and a repetition frequency of 10\\u00a0Hz. The intensity of the perturbation laser pulse was controlled to maintain the amplitude of transient VOC below 5\\u00a0mV so that the perturbation assumption of excitation light holds. The voltages under open circuit and currents under short-circuit conditions were measured over a 1 M\\u03a9 and a 50\\u00a0\\u03a9 resistor and were recorded on a digital oscilloscope (Tektronix DPO 4104B).\\n\\nUV-vis absorption spectra of the PVSK films were obtained using a U-4100 spectrophotometer (Hitachi) equipped with integrating sphere in which monochromatic light was incident to the substrate side. XRD patterns of the films were recorded by X-ray diffractometer (PANalytical) with Cu k\\u03b1 radiation at a scan rate of 4\\u00b0/min. Surface and cross-sectional microscopic images of the films and devices were acquired by SEM (Nova Nano 230). \\u223c1-nm-thick gold was sputtered on cross-sectional samples to enhance the conductivity. Transmission Fourier transform infrared (FTIR) spectroscopic analysis was performed using FT/IR-6100 (Jasco). The chamber was purged with nitrogen gas during the measurement. Steady-state PL measurement was carried out using Horiba Jobin Yvon system in which a 640\\u00a0nm monochromatic laser was used as an excitation fluorescence source. Time-resolved PL decay profiles of the PVSK films were investigated by a Picoharp 300 with time-correlated single-photon counting capabilities. A 640\\u00a0nm monochromatic pulsed laser with a repetition frequency of 100 kHz was generated from a picosecond laser diode head (PLD 800B, PicoQuant). The energy density of the excitation light was controlled to be \\u223c1.4 nJ/cm2.\\nGIWAXS test was performed at the BL14B1 beamline of China Shanghai Synchrotron Radiation Facility (SSRF). 2D GIWAXS patterns were obtained by a MarCCD 225 detector mounted vertically at around 256.401\\u00a0mm from the sample with an exposure time of 50\\u00a0s at a grazing incidence angle of 0.15\\u00b0. The x axis of GIWAXS patterns were represented by the diffraction vector with q\\u00a0= 4\\u03c0sin(\\u03b8)/\\u03bb, where \\u03b8 is half of the diffraction angle and \\u03bb is the wavelength of incident X-ray. XPS measurements were carried out on an XPS AXIS Ultra DLD (Kratos Analytical). An Al K\\u03b1 (1,486.6\\u00a0eV) X-ray was used as the excitation source. UPS measurements were carried out to determine the work function and the position of valence band maximum of materials. A He discharge lamp, emitting ultraviolet energy at 21.2 eV, was used for excitation. All UPS measurements were performed using standard procedures with a \\u22129\\u00a0V bias applied between the samples and detectors. Clean gold was used as a reference. High angle annular dark field scanning transmission electron microscopy (HAADF STEM) images, EDS maps, and line-scan profiles were taken on a FEI Titan STEM operated at 300 kV. The device glass, ITO, SnO2, PVSK, PTAA, and Ag was used for the TEM sample. The focused ion beam technique was used for cross-TEM sample preparation. HRTEM analysis was performed by Titan (FEI). The PVSK film was scratched off from the substrate and dispersed in toluene by sonication for 10\\u00a0min, which was dropped on a copper grid. Accelerating voltage of 300 kV was used for the measurement. TGA was conducted using SDT Q600 (TA instruments) under dry air with a heating rate of 10\\u00b0C/min.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Caffeine,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65,\\n Perovskite_deposition_thermal_annealing_time: 1,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 40.0; 40.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 500,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 90,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A majority of materials were purchased from Alfa-Aesar without further purification. PETG-1 was synthesized and purified by ourselves. PbI2 and n-DMBI was obtained from Xi'an Polymer Light Technology Corp. and Sigma Aldrich, respectively. Methylammonium iodide (MAI) was synthesized by the reaction of 24\\u202fmL CH3NH2 (33\\u202fwt% in absolute ethanol, Alfa) and 30\\u202fmL HI (57\\u202fwt% in water, Alfa) at 0\\u202f\\u00b0C stirring for 2\\u202fh. The precipitate of MAI was then evaporated at 55\\u202f\\u00b0C for 1\\u202fh. Then, the MAI powder was washed three times with diethyl ether by stirring the solution for oven 30\\u202fmin before being dried in a vacuum at 60\\u202f\\u00b0C for 48\\u202fh, finally stored in N2 atmosphere. The CH3NH3PbI3 precursor solution was fabricated by following the method, where 1152\\u202fmg of PbI2, 398\\u202fmg of MAI, and 400\\u202f\\u03bcL of DMSO were mixed with 1600\\u202f\\u03bcL of DMF. Then, the solution was stirred for oven 12\\u202fh\\u202fat 65\\u202f\\u00b0C in a N2-filled glovebox.\\n\\nThe perovskite solar cells were fabricated on fluorine-doped tin oxide (FTO) coated glass (8\\u202f\\u03a9/sq) with the following device configuration: FTO/ETL/CH3NH3PbI3/Spiro-OMeTAD/Au. The FTO glass was cleaned by sequential ultrasonic treatment cleaning in de-ionized water, acetone, ethyl alcohol and isopropyl alcohol for 15\\u202fmin each orderly, and then dried at room temperature. After drying, the substrates were treated within a UV-ozone chamber for 15\\u202fmin to remove the organic residues. Firstly, thick electron extraction layer (50\\u202fnm) was spin-coated on top of the FTO glass from solutions of PTEG-1 and PTEG-1 doped with a variable ratio, respectively. Secondly, for the deposition of perovskite film, the as-prepared fresh CH3NH3PbI3 precursor solution was spin-coated on the PTEG-1 film, and then annealed at 100\\u202f\\u00b0C for 10\\u202fmin. Specifically, the CH3NH3PbI3 precursor solution was dropped to cover the active device area, and immediately the spin-coating recipe was initiated via two consecutive steps of 1500\\u202fr.p.m. for 15\\u202fs and then 4000\\u202frpm for 20\\u202fs. In the last 5\\u202fs, 300\\u202f\\u03bcL toluene of was dropped at the center of this substrate to drive mixed DMSO/DMF solvent away. Thirdly, the HTL was spin-coated on the perovskite layer by 3000\\u202fr.p.m. for 30\\u202fs. The precursor solution was prepared by dissolving 144.6\\u202fmg Spiro-OMeTAD, 57.6\\u202f\\u03bcL 4-tert-butylpyridine, and 35\\u202f\\u03bcL bis(trifluoromethane) sulfonamide lithium salt (Li-TFSI) solution (LiTFSI, 520\\u202fmg/mL in acetonitrile) in 2\\u202fmL chlorobenzene. Finally, 80\\u202fnm of Au was thermal deposited as a counter electrode through a shadow mask using a Trovato thermal evaporator. The active device area was 0.04\\u202fcm2.\\n\\nThe current density-voltage (J\\u2013V) characteristics were obtained using a Keithley 2400 source meter and a collimated Xenon lamp (300\\u202fW, Newport) calibrated with the light intensity of 100\\u202fmW\\u202fcm\\u22122 under the simulated one-sun AM 1.5\\u202fG solar irradiance in ambient air. The J\\u2013V curves were carried out under both forward and reverse scan in the range from 0 to 1.2\\u202fV. Scanning electron microscopy (SEM) images were acquired by using a field-emission scanning electron microscope (JEM-4800F). The incident photon-to-electron conversion efficiency (IPCE) was recorded by a computer-controlled IPCE system (Newport). Photoluminescence (PL) (excitation at 470\\u202fnm) and the time-resolved photoluminescence (TRPL) decay measurements were prepared using a FLSP920 spectrometer (Edinburgh Instruments LTD). Impedance spectroscopic measurement was carried out using an electrochemical analyzer (Autolab 320, Metrohm, Switzerland) with a constant reverse potential from 0 to 1\\u202fV in the dark. The crystal structure of the perovskite thin films was performed by a Rigaku (RINT-2500) X-ray diffraction patterns (Cu Ka radiation, \\u03bb\\u202f=\\u202f1.5418\\u202f\\u00c5).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PTEG-1,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 60.0; 60.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 39,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals were used as received, including PbI2 (99.9985%, Alfa Aesar), CH3NH3I (MAI, Xi\\u2019an Polymer Light Technology Corp), SnCl2\\u00b72H2O (ACS, 98\\u2013103%, Alfa Aesar), Spiro-OMeTAD (99.7%, Lumtec Co., Taiwan). Titanium(IV) isopropoxide (99.999%), 4-tert-butylpyridine (TBP, 96%), Bis(trifluoromethane)sulfonimide lithium salt (99.95%), and solvents of acetonitrile (99.9%), ethanol (99.8%), dimethylformamide (DMF, 99.8%), dimethylsulfoxide (DMSO, 99.9%), and chlorobenzene (99.8%) were all purchased from Sigma Aldrich. FTO glasses (FTO, 7 \\u03a9/sq) were purchased from Yingkou OPVtech New Energy Co. LTD.\\n\\nSnCl2\\u00b72H2O solution (0.1 M) was prepared by dissolving SnCl2\\u00b72H2O in anhydrous alcohol in a flask, then the solution was stirred at room temperature or 80 \\u00b0C with the neck of flask sealed to prevent O2 and H2O into the solution for 3 h. To obtain SnO2 organic sol, the just dissolved SnCl2\\u00b72H2O solution was transferred to an open reflux apparatus, then refluxing for different time at different temperature. When the reaction is over, the product was aged for over 24 h at room temperature.\\n\\nFTO glasses were etched with zinc powder and 1 M HCl to obtain the electrode pattern, and then washed with cleaning fluid, deionized water, ethanol (99.7%, Sinopharm), acetone (99.5%, Beijing Shiji) and isopropanol (99.7%, Sinopharm) sequentially. To prepare SnO2 ETLs, SnO2 sol or SnCl2\\u00b72H2O solution was spin coated on FTO at 2000 rpm for 30 s, and then heated at different temperature for 1.5 h to remove solvent. Then, the as-deposited ETLs were treated with UV-Ozone for 20 min. TiO2 ETL was prepared as reported . Typically, a mildly acidic solution of titanium isopropoxide in ethanol (the concentrations of titanium isopropoxide/2 M HCl/ethanol = 254 \\u03bcL/34 \\u03bcL/2 mL) was spin-coated on the cleaned FTO at 2000 rpm for 60 s, then annealed in air at 500 \\u00b0C for 30 min. Finally, the ETL substrates were transferred to the glove box (H2O content lower than 0.01 ppm) for perovskite deposition.\\n\\nPerovskite of (FAPbI3)0.85(MAPbBr3)0.15 was prepared according to previous report . Firstly, anhydrous mixture of DMF and DMSO (volume ratio is 4:1) containing FAI (1 M), PbI2 (1.1 M), MABr (0.2 M) and PbBr2 (0.2 M) was prepared firstly by stirring at 70 \\u00b0C for 2 h. Then, 80 \\u03bcL solution was spread on the FTO/ETL substrate followed by a two-stage spin coating processes (1000 rpm for 10 s and 6000 rpm for 50 s). During the second spin coating stage, 100 \\u03bcL of chlorobenzene were poured on the spinning substrate 25 s prior the end of the program. Finally, the substrates were annealed at 100 \\u00b0C for 40 min.\\n\\nPrecursor solution of hole transfer layer (HTM) was prepared by dissolving 72.3 mg spiro-MeOTAD, 28.8 \\u03bcL 4-tert-butylpyridine, 17.5 \\u03bcL lithium bis(trifluoromethylsulphonyl)imide acetonitrile solution (520 mg mL\\u22121) into 1 mL chlorobenzene. Then, HTM layer was deposited atop perovskite by spin coating at 3000 rpm for 30 s. Finally, a 60 nm Au electrode was thermally evaporated on top of the device under high vacuum (< 10\\u22124 Pa). The active area of the device was 0.16 cm2, defined by the aperture area of the mask.\\n\\nUV\\u2013vis absorption spectra were recorded with a spectrophotometer (Hitachi, Ltd., U-3900). The crystal structures of ETLs were characterized using a Bruker D8 ADVANCE X-ray diffractometer. TEM and HRTEM analysis were carried out on a JEOL JEM-2100F microscope. SEM images were acquired with a field-emission scanning electron microscope (FE-SEM, JEOL JSM-7401F). Ultraviolet photoelectron spectroscopy (UPS) characterizations were performed by monochromatized HeI radiation at 21.2 eV. Linear sweep voltammetry (LSV) curves of ETLs were measured using a Keithley 2400 source, and the design pattern for LSV measurement is shown in Fig. S1. The time-resolved PL spectra were measured using an Edinburgh Instruments FLS920 spectrometer by the time correlated single photon counting (TCSPC) technique. An EPL 515 nm pulsed diode laser was used for excitation with repetition rates at 10 MHz. The maximum average power was 5 mW and all samples were measured at the same intensity with an instrument response function (IRF). The emission wavelength was set at 765 nm. The photocurrent-voltage (J-V) characteristics of the devices were measured with a Keithley 2400 digital source meter at the scan speed of 100 mV s\\u22121. The simulated AM 1.5G sunlight with an irradiance equivalent to 100 mW cm\\u22122 was generated by a Oriel Solar 3A solar simulators and the intensity was calibrated with an VLSI standards incorporated PN 91150V Si reference cell. The cells were masked using a black metal mask with a hole area of 0.096 cm2. Steady-state output of photocurrent and PCE were measured with Keithley 2400 digital source meter under a certain bias. The incident photonto-electron conversion efficiency (IPCE) spectra were recorded by a setup, consist of a xenon light source, a monochromator, and a potentiostat.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 20.0; 20.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 100,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 96.3,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium (CH3NH2), Lead chloride (PbI2, 99.99%), hydroiodic acid (HI, 57\\u202fwt% in water), Spiro-OMeTAD, Anhydrous dimethyl sulfoxide (DMSO), and \\u03b3-butyrolactone were purchased from Sigma Aldrich.\\n\\nThe TiOx precursor solution was prepared by adding dropwise pure TiCl4 (4.5\\u202fmL) solution onto ice cubes (200\\u202fmL) in ambient air environment which melted naturally. MAI and PbI2 powder were mixed in DMSO:GBL (7:3, v/v) blend with a molar ratio of 1:1 to make the perovskite precursor solution. The resultant perovskite precursor solution was stirred at 70\\u202f\\u00b0C overnight and then filtered through PTFE filters (0.22\\u202f\\u00b5m) before usage in a glovebox. Spiro-OMeTAD solution was prepared by mixing 17.5\\u202f\\u00b5L lithiumbis (trifluoromethanesulfonyl) imide (TFSI-Li) solution (520\\u202fmg Li-TFSI in 1\\u202fmL acetonitrile) and 28.5\\u202f\\u00b5L 4-tertbutylpyridine with 80\\u202fmg Spiro-OMeTAD in 1\\u202fmL chlorobenzene (CB) solution. The HI CB solution was prepared by adding 0\\u20133.33\\u202fvol% of HI into CB solution with a small amount of isopropanol (10\\u202f\\u00b5L IPA / 1\\u202fmL CB).\\n\\nPatterned ITO substrates were thoroughly cleaned in ultrasonic bath using acetone, ethanol, and deionized water in sequence for 15\\u202fmin, respectively. To prepare the nanocrystalline TiO2 hole-blocking layer, the substrates were immersed into the TiOx precursor solution at 70\\u202f\\u00b0C for 1\\u202fh, and then heated for 1\\u202fh at 100\\u202f\\u00b0C in a baking oven in ambient air environment . Fig. 1a illustrates the present fabrication process for the perovskite films. After the precursor solution was spin coated onto the TiO2 layer at 4000\\u202frpm for 20\\u202fs, the HI CB solution with different volume ratios was dripped on the precursor films during the spin-coating process for another 20\\u202fs. Subsequently, the precursor film are annealing at 100\\u202f\\u00b0C for 10\\u202fmin in nitrogen glove box to obtain the perovskite layer. To fabricate the PSCs, the solution of spiroOMeTAD was spin-coated onto the perovskite layer at 2000\\u202frpm for 40\\u202fs in the glovebox. And then the spiroOMeTAD layer was oxidated for about 8\\u201310\\u202fh in ambient air environment. Finally, the device was transferred to a vacuum chamber at 2\\u202f\\u00d7\\u202f10\\u22126 Torr for MnOx and Au electrode evaporation. The active area of each device is 0.09\\u202fcm2 as determined by the shadow mask. For the preparation of the flexible PSCs, all the procedures are the same to those for the planar PSCs described except on PET/ITO substrates.\\n\\nThe current density-voltage characteristics of the PSCs were measured by using a programmable Keithley 2400 source meter under AM 1.5\\u202fG solar irradiation at 100\\u202fmW/cm2 (Newport, Class AAA solar simulator, 94023A-U). The field-emission scanning electron microscope (SEM) images were obtained from a Quanta 200 FEG. The grazing incidence X-ray diffraction (GIXRD) and in-situ tensile XRD were performed at the BL14B1 beamline of the Shanghai Synchrotron Radiation Facility (SSRF) using X-ray with a wavelength of 0.6887\\u202f\\u00c5 . The in-situ tensile XRD experimental was measured by the Transmission mode, and the flexible PSCs were sticked on the lateral side of sample holder and placed at the vertical of X-ray incidence direction. Two-dimensional XRD patterns were acquired by a MarCCD at a distance ~271\\u202fmm vertically from the sample with an exposure time of 20\\u202fs. The grazing incidence angles of 0.05\\u00b0, 0.10\\u00b0, 020\\u00b0 and 0.30\\u00b0 were adopted to achieve depth-dependent information. The XRD patterns were analyzed using the FIT2D software and displayed in scattering vector q coordinates. To map I and Pb distribution, EPMA were carried out with an accelerating voltage of 10\\u202fkV by collecting characteristic X-rays. AFM and SKPM measurements were obtained using a scanning probe microscope (Keysight 5500). In the thermal stability test, the XRD spectra were recorded by a lab Bruker D4 diffractometer with a copper target X-ray tube. Photoemission spectroscopy (PES) measurements were performed at the photoemission spectroscopy (BL10B) beamline of National Synchrotron Radiation Laboratory (NSRL). For the PES measurements, N2 protected samples were transferred into an ultrahigh vacuum (VHV) chamber with a base pressure of 5\\u202f\\u00d7\\u202f10\\u221210 mbar after less than 20\\u202fmin air exposure.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 312,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 20,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Prior to fabrication of the perovskite solar cells, indium tin oxide (ITO) substrates were rinsed in diluted detergent followed by sonification in water, acetone and ethyl alcohol in sequence. For formation of NiOx thin-film, a 1\\u202fmmol of nickel(II) acetate tetrahydrate (\\u2265 99.0% purity) was dissolved in 10\\u202fmL of ethyl alcohol by sonification. The prepared solution was coated on the ITO glass substrates by spin-coating at 66.7\\u202fHz (4000\\u202frpm) for 45\\u202fs, and the coated substrate was annealed at 300\\u202f\\u00b0C for 1\\u202fh. The perovskite solution containing PbI2 (99.99985% purity) and methylammonium iodide (1:1\\u202fM ratio, 0.54:1\\u202fwt ratio) in a mixture of N,N-dimethylformamide (99.8% purity) and dimethyl sulfoxide (DMSO) (\\u2265 99.9% purity) (9:1 by volume) was deposited by two step spin-coatings made at 16.7\\u202fHz (1000\\u202frpm) 15\\u202fs and 75\\u202fHz (4500\\u202frpm) for 25\\u202fs, respectively. During the second step, a droplet of diethyl ether was deposited on the substrate and soon after the substrate was transferred to a hot plate for annealing at 100\\u202f\\u00b0C and 130\\u202f\\u00b0C for 10\\u202fmin. Subsequently, the [6,6]-phenyl C61 butyric acid methyl ester ([60]PCBM, 99.5% purity) solution (20\\u202fmg\\u202fmL\\u22121 in chlorobenzene) was spin-coated at 33.3\\u202fHz (2000\\u202frpm) for 60\\u202fs. Finally, a 120\\u202fnm-thick Ag counter electrode was deposited by thermal evaporation.\\n\\nA tapered optical fiber (50\\u202f\\u00b5m core diameter/125\\u202f\\u00b5m cladding diameter) with small aperture (\\u2248 200\\u202fnm) in the metal coating is attached to a quartz tuning fork-based atomic force microscopy (AFM) probe. Light of a diode laser (a wavelength of 635\\u202fnm) is coupled to the optical fiber for local light injection. The perovskite solar cell is placed on a xyz piezo stage for NSPM. The topography and photocurrent were obtained simultaneously during the raster scanning made by the NSOM probe. The amplified photocurrent (with a gain of 107 V/A from a variable-gain low-noise current amplifier) is measured based on a lock-in technique.\\n\\nThe current density-voltage (J-V) measurements were performed under AM1.5\\u202fG 1 sun illumination (100\\u202fmW/cm2) using a solar simulator.\\n\\nTo observe light-induced property changes, perovskite solar cells were continuously exposed to light up to 900\\u202fmin of AM1.5\\u202fG 0.1 sun illumination (10\\u202fmW/cm2). For every 100\\u202fmin of light illumination, J-V and NSPM measurements were performed. Other environmental factors (e.g., temperature, relative humidity in air) were controlled to isolate the effect of light illumination on devices.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 15,\\n Stability_PCE_initial_value: 16.9,\\n Stability_PCE_end_of_experiment: 25,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite solar cells were fabricated on FTO (NSG10) substrates previously cleaned by a sequential sonication treatment in a 2% Hellmanex solution, acetone and isopropanol, followed by UV ozone treatment for 20\\u2009min. Then samples were heated to 500\\u2009\\u00b0C and a compact blocking layer of TiO2 was then deposited onto the FTO glass substrate by spray pyrolysis, using a dilution 1/19\\u2009ml of titanium diisopropoxide bis(acetylacetonate) solution in ethanol keeping them for 30\\u2009min. Next, a mesoporous TiO2 (30 NRD from Dyesol) was prepared by spin-coating a diluted TiO2 dispersion in ethanol, ratio 1:8 (w/v), at 2000\\u2009rpm (1000\\u2009rpm/s acceleration) for 10\\u2009s followed by a progressive heating step till 500\\u2009\\u00b0C for 30\\u2009min. Afterwards, the substrates were treated with tris(bis(trifluoromethylsulfonyl)imide) (Li-TFSI) by spin-coating 50\\u2009\\u03bcl onto the mesoporous layer, followed by a sintering step at 500\\u2009\\u00b0C for 30\\u2009min. The solution and perovskite films were prepared inside an argon glove box under moisture and oxygen controlled conditions (H2O level:1\\u2009ppm and O2 level:10\\u2009ppm) and kept under stirring at 80\\u2009\\u00b0C overnight in order to dissolve completely PbI2. Stoichiometric precursor solutions (1.25\\u2009M) were prepared by mixing MAI (Sigma Aldrich) and PbI2 (TCI) in N,N\\u2019-dimethylsulfoxide (DMSO). The perovskite layers were then fabricated by using a two-steps spin-coating process, first step 1000 r.p.m. for 10\\u2009s; second step 3500 r.p.m for 30\\u2009s. During the second step 110\\u2009\\u03bcl of chlorobenzene were poured onto the films 10\\u2009s prior to the end of the program, and then substrates were annealed at 100\\u2009\\u00b0C during 40\\u2009min. Once the samples were cool down, Imidazolium iodide at different concentration (2.5, 5,10 and 20\\u2009mg/ml) were droped on perovskite layers for spin-coating at 3500 r.p.m for 30\\u2009s and kept at 100\\u2009\\u00b0C for 10\\u2009min. When samples reach room temperature, Spiro-OMeTAD was then spun coated at 4000\\u2009rpm for 30\\u2009s by dissolving 72.3\\u2009mg of Spiro-OMeTAD in 1\\u2009ml of chlorobenzene; 21.9\\u2009ml of tris(2-(1H-pyrazol-1-yl)\\u22124-tert-butylpyrydine) cobalt(III) bis(trifluoromethylsulphonyl) imide (FK209) from stock solution (400\\u2009mg of FK209 in 1\\u2009ml of acetonitrile), 17.5\\u2009ml of lithium bis-(trifluoromethylsulphonyl) imide (LiTFSI) stock solution (520\\u2009mg of LiTFSI in 1\\u2009ml of acetonitrile) and 28.8\\u2009ml of 4-tert-butylpyridine were also added to the solution as dopants. Finally, 70\\u2009nm of gold was deposited by thermal evaporation.\\n\\nFor structural characterization, thin films were prepared by spin coating of MAPbI3 and MAPbI3 +\\u2009ImI solutions onto glass. X-ray diffractograms were recorded using a D8 Advance diffractometer from Bruker (Bragg-Brentano geometry, with an X-ray tube Cu K\\u03b1, \\u03bb\\u2009=\\u20091.5406\\u2009\\u00c5). A scan range of 3\\u201380\\u00b0 was selected with an acquisition time of 1 degree per min. The absorption spectra were registered with an UV\\u2013VIS\\u2013IR spectrophotometer (PerkinElmer Instrument). Photoluminescence (PL) steady-state measurements were recorded with a spectrophotometer (Gilden Photonics) Time-resolved PL signals were acquired using a Time Correlated Single Photon Counting detection technique with a time resolution of 1 ns.\\n\\nCurrent density\\u2013voltage (J\\u2013V) curves were recorded using a VeraSol LED solar simulator (Newport) producing 1 sun AM 1.5 (1000\\u2009W/m2) sunlight. Current-voltage curves were measured in air with a potentiostat (Keithley 2604). The light intensity was calibrated with a NREL certified KG5 filtered Silicon reference diode. J-V measurement were performed at 100\\u2009mV\\u2009s-1 scan rate (pre sweep delay: 10\\u2009s) and a black metal mask (0.16\\u2009cm2) was used over the square solar cell active area to reduce the influence of scattered light. The stability test was performed in a sealed cell holder flushed with inert gas flow (Ar, 30\\u2009ml/min) and I-V curves were characterized by an electronic system using 22 bits delta-sigma analogical to digital converter. Cells were maintained at the maximum power point using a MPPT algorithm under 100\\u2009mW/cm2, maintaining the temperature of the cells around 60\\u2009\\u00b0C. A reference Si-photodiode was placed in the holder to verify the stability of the light. Incident photon current efficiency (IPCE) measurements were carried out using a 150\\u2009W Xenon lamp (Newport) attached to with IQE200B (Oriel) motorized 1/4\\u2009m monochromator as the light source.\\nElectro-chemical Impedance Spectroscopy (EIS) measurements were carried out altering the positions of the Fermi level by a white LED source. Samples were kept inside a faradaic chamber to avoid external interferences and with a nitrogen atmosphere to avoid degradation. A 20\\u2009mV perturbation in the range 2MHz\\u20131mHz\\u00a0was used to obtain the spectra. After measurement, data were fitted by Z-view software in order to extract characteristic parameters of the cells.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: Imidazonium iodide | Spiro-MeOTAD,\\n HTL_additives_compounds: Unknown | FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 60.0; 60.0,\\n Stability_atmosphere: Ar,\\n Stability_time_total_exposure: 300,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the materials, such as cesium iodide (CsI, 99.998%, Alfa-Aesar), lead iodide (PbI2, 99.999%, Sigma), lead bromide (PbBr2, 99.999%, Alfa-Aesar), Dimethyl sulphoxide (DMSO, 99.8%, Sigma), SnO2 colloid precursor (tin (IV) oxide, Alfa-Aesar), Spiro-OMeTAD (Xi'an Polymer Light Technology Corp.), tris[2-(1H-pyrazol-1- yl)-4-tert-butylpyridine] cobalt (III) tris [bis- (turfluoromethylsuflonyl)imide] (FK209, Dyesol), bis- (trifluoromethance) solfonimide lithium salt (LiTFSI, 96% purity, Sigma-Aldrich), 4-tBP (96% purity, Sigma-Aldrich) were used as received without further purification.\\n\\nThe indium tin oxide (ITO) glass substrates (10\\u202f\\u03a9 sq\\u22121) were cleaned by ultrasonic treatment with detergent, deionized water, acetone and ethyl alcohol for 20\\u202fmin and dried with nitrogen. Then, the ITO substrates were treated with UV-ozone for 20\\u202fmin to remove organic residues. SnO2 colloid precursor was diluted to 5% with deionized water. A thin layer of SnO2 nanoparticle film was spin-coated at 4000\\u202frpm for 30\\u202fs and annealed at 150\\u202f\\u00b0C for 30\\u202fmin. PbI2: PbBr2: CsI (0.6\\u202fM: 0.6\\u202fM: 1.2\\u202fM) were dissolved in DMSO (1\\u202fmL) and stired all night. The prepared precursor solution was filtered with filter (0.22 \\u03bcm). The precursor solution was spin-coated on the SnO2 substrate at 3000\\u202frpm for 30\\u202fs. Then the CsPbI2Br film annealed via sequential graded thermal annealing process at 50\\u202f\\u00b0C for 3\\u202fmin and 160\\u202f\\u00b0C for 10\\u202fmin. Then, the Spiro-OMeTAD film was spin-coated on the CsPbI2Br perovskites film at 1000\\u202frpm for 10\\u202fs and 4000\\u202frpm for 30\\u202fs. The Spiro-OMeTAD solution contained 72.5\\u202fmg Spiro-OMeTAD, 18 \\u03bcL of LiTFSI stock solution (520\\u202fmg/mL in acetonitrile) and 29 \\u03bcL of FK209 solution (300\\u202fmg/mL in acetonitrile) and 29 \\u03bcL of tBP. A thin film of MoO3 (8\\u202fnm) was thermally evaporated under vacuum with evaporation rate of 0.3\\u202f\\u00c5/s. Finally, 100\\u202fnm Ag electrodes were thermally evaporated to finish the device fabrication. All the devices had an effective area of 7.5\\u202fmm2 defined by the metal shadow mask.\\n\\nAll the devices were measured via using Keithley 2400 under standard solar simulator with an intensity of 100\\u202fmW/cm2. The system was calibrated against a NREL certified silicon reference solar cell. All the measurements of the solar cells were performed under ambient atmosphere at room temperature without encapsulation. IPCE measurements were carried out on the SCS10-X150 systems (Zolix instrument. Co. Ltd). XRD measurements were performed by Bruker D8 Advance XRD. The UV-vis absorption spectra were measured with Perkin-Elmer Lambda 950 spectrophotometer. PL and TR-PL spectra were recorded via using the Pico Quant Fluotime 300 with a 510\\u202fnm\\u202fps pulsed laser. The morphology characterization of the films was measured by SEM (JSM-7800F). XPS measurements were performed by the Escalab 250Xi with a source of monochromatic Al-Ka (1486.6\\u202feV). Transient photocurrent (TPC) measurement was performed with a system excited by a 532\\u202fnm (1000\\u202fHz, 3.2\\u202fns) pulse laser. Transient photovoltage (TPV) measurement was performed with the same system excited by a 405\\u202fnm (50\\u202fHz, 20\\u202fms) pulse laser. A digital oscilloscope (Tektronix, D4105) was used to record the photocurrent or photovoltage decay process with a sampling resistor of 50\\u202f\\u03a9 or 1\\u202fM\\u03a9, respectively.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBrI2,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 50; 160,\\n Perovskite_deposition_thermal_annealing_time: 3.0; 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 3,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 30,\\n Cell_area_measured: 0.075,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials preparation: The (Zn2+ doped) CuGaO2 nanocrystals were synthesized as follows: 1.4\\u202fmmol\\u202fGa(NO3)3\\u00b7xH2O, x mmol Zn(NO3)2\\u00b76H2O and 1.4\\u202fmmol Cu(NO3)2\\u00b73H2O were dissolved in 14\\u202fmL deionized water. Then 8\\u202fmL ethylene glycol and 6\\u202fmL of 0.5\\u202fM KOH solution were slowly added with stirring in an ice bath or water bath (around 3\\u202f\\u00b0C). After stirring for 1\\u202fh, the precursor was transferred into a 50\\u202fmL Teflon-lined autoclave (Chengdu Xinyi instrument co. LTD) and kept at 200\\u202f\\u00b0C for 24\\u202fh. Then the powder was collected by centrifugation (8000\\u202frpm for 10\\u202fmin) and washed sequentially with diluted ammonia hydroxide (9.5%\\u201310.5% (g/mL)), diluted HNO3 solution (10\\u202fwt%), and deionized water. This process was repeated for five times. Finally, the Zn2+ doped CuGaO2 Nanocrystals was stored in absolute isopropanol solution for further use.\\nDevice fabrication: Devices were prepared on cleaned and patterned FTO substrates. The dense NiOx was prepared via electron beam evaporation (zzsx-500, Beijing instrument co.LTD) with a deposition rate of 0.01\\u202fnm/s. And then 50\\u202fmg of (Zn2+ doped) CuGaO2 powdered materials was mixed with 400\\u202f\\u03bcL isopropyl alcohol. This mixture was then ultrasonicated for 30\\u202fmin and poured dropwise in 3.32\\u202fmL of Terpineol and 4\\u202fmL of isopropyl alcohol/ethylcellulose (9:1) to form the paste with a suitable viscosity, and then the paste was deposited on NiOx-coated FTO substrates (Pilkington TEC8, 14\\u202f\\u03a9/sq) by spin coating. The mesoporous (Zn2+ doped) CuGaO2 films can be obtained after annealing at 350\\u202f\\u00b0C for 30\\u202fmin to burn off the organic. The perovskite layer was deposited by using a green solvent processed method in a nitrogen filled glovebox. The precursor solution is comprised of 52\\u202fmg of CsI, 174\\u202fmg of FAI, 560\\u202fmg of PbI2, 50\\u202fmg of PbBr2, 17\\u202fmg of FABr in 1\\u202fmL of dimethyl formamide (DMF) and dimethylsulfoxide (DMSO) (4:1, v/v). The solution was spin-coated onto the (Zn2+ doped) CuGaO2 substrates by a consecutive two-step spin-coating process at 1000 and 5000\\u202frpm for 10 and 40\\u202fs, respectively. During the second spin-coating step, 120\\u202f\\u03bcL anisole was dropped onto the substrate after 20\\u202fs. And then the substrate was annealed at 100\\u202f\\u00b0C for 20\\u202fmin. An electron-transporting layer was coated with a solution of PC61BM dissolved in anisole (20\\u202fmg\\u202fmL\\u22121) at 3000\\u202frpm for 30\\u202fs and followed by a BCP/isopropanol solution (0.5\\u202fmg\\u202fmL\\u22121) at 5000\\u202frpm for 30\\u202fs. Finally, a 100\\u202fnm thick Ag electrode was deposited by thermal evaporation to complete the device fabrication.\\nCharacterization: The XRD was measured on Maxima 7000 diffractometer (Shimadzu, Japan) with a Cu K\\u03b1 radiation (40\\u202fkV, 100\\u202fmA). Energy levels of CuGaO2 were detected by Thermo escalab 250XI. The film morphology was obtained by using a Titachi S5200 field-emission scanning electron microscope (Hitachi High Technologies Corporation). The UV visible spectra were measured using an Evolution\\u2122 201 spectrophotometer (Thermo fisher scientific Corporation). The nanoplate morphology, elemental mapping and lattice spacing is examined by transmission electron microscopy (Carl Zeiss SMT Pte, Ltd Libra 200FE) at 200\\u202fkV. The steady PL spectra and time-resolved PL decay measurements were performed using an HORIBA DeltaFlex system (HORIBA) with an excitation wavelength at 510\\u202fnm. Repetition rate were 100\\u202fMHz and 2\\u202fMHz, respectively. The atom force microscopy (AFM) date was obtained on a Dimension Icon (broker Corporation). Calibrating of Roughness value, root-mean-square (RMS), and Graphics processing were taken on NanoScope Analysis. Tafel and J-V plots of the hole-extracting only devices were characterized by Keithley 2400 Source in dark. The space-charge limited current (SCLC), electrochemical impedance spectroscopy (EIS) and Mott-Schottky plot were obtained by using a multi-channel potentiostat (VMP3, Biologic) under dark conditions. For the Mott-Schottky analysis, the electrodes were submerged in a 0.1\\u202fM KCl aqueous solution, with a Pt counter electrode and Ag/AgCl reference electrode. The values were recorded at frequency of 80\\u202fmHz. EIS datas were recorded at 0 and 0.8\\u202fV in the frequency range from 1\\u202fMHz to 100\\u202fmHz with an alternating current (AC) amplitude of 30\\u202fmV. The Mott-Schottky data were recorded at the frequency of 80\\u202fmHz in the applied voltage range from \\u22120.6\\u202fV to 0.6\\u202fV with an AC amplitude of 30\\u202fmV. The current-voltage characteristics were measured by Keithley 2400 source and the solar simulator with standard AM 1.5G (100\\u202fmW\\u202fcm\\u22122, SSF5-3\\u202fA: Enlitech) under ambient conditions. The J-V curves for the devices were measured by forward (\\u22120.1\\u202fV\\u20131.2\\u202fV forward bias) or reverse (1.2\\u202fV to \\u22120.1\\u202fV) scans with a scan rate of 100\\u202fmV/s, which is usually employed in literature. J-V curves for all devices were obtained by masking the cells with a metal mask 0.09\\u202fcm2 in area. Monochromatic incident photon-to-current conversion efficiency (IPCE) spectra were recorded as functions of wavelength with a monochromatic incident light of 1\\u202f\\u00d7\\u202f1016 photons cm\\u22122 in AC mode with a bias voltage of 0\\u202fV (QE-R3011). The light intensity of the solar simulator was calibrated by a standard silicon solar cell provided by PV Measurements.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs0.15FA0.85PbBr0.12I2.88,\\n Perovskite_composition_short_form: CsFAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: NiO-c | CuGaO2,\\n HTL_additives_compounds: Unknown | Zn,\\n HTL_deposition_procedure: E-beam evaporation | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 85.0; 85.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 1000,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 87,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Regioregular poly(3-hexylthiophene) (SMI-P3HT, Mn\\u00a0=\\u00a05.0\\u00a0\\u00d7 104\\u00a0g/mol, PDI\\u00a0=\\u00a01.7, regioregularity Rr\\u00a0=\\u00a095%), Poly[(ethylhexyl)-thiophenyl]-benzodithiophene-(ethylhexy)-thienothiophene] (PTB7-Th), and phenyl-C61-butyric acid methyl ester (PC61BM) were purchased from Solarmer Energy, Inc. (Beijing). Branched polyethylenimine (PEI, Mn\\u00a0=\\u00a02.5\\u00a0\\u00d7\\u00a0104\\u00a0g/mol) was purchased from Sigma-Aldrich.\\n\\nZnO colloidal particles with size of 5\\u20137\\u00a0nm were synthesized through reaction of KOH and Zn(OAc)2 in methanol solvent as reported by Beek et\\u00a0al. For the use in the organic solar cells, the ZnO colloidal particles were centrifuged in methanol for 3 times and finally dispersed in a mixture solvent of chloroform and methanol. The concentration of ZnO ranges from 10 to 56\\u00a0mg/mL for different ZnO:PEI thickness. Branched PEI was dissolved in methanol in 0.21\\u00a0mg/mL. The ZnO and PEI inks were mixing with volume ratios of 1:1 to form ZnO:PEI composite inks. For the use of ZnO in the perovskite solar cells, the ZnO colloidal particles were dispersed in a mixture solvent of methanol and butanol with concentration of 10\\u00a0mg/mL. The ZnO and PEI inks were mixed together with volume concentration of 1:1.\\n\\nThe film morphology was determined through Atomic Force Microscopy (AFM, Dimension 3100) in tapping mode. Thin film for the ultraviolet photoelectron spectroscopy (UPS) was prepared on the cleaned ITO glass by the same procedure as for the preparation the CBL for solar cell devices (vide infra).\\n\\nThe used ITO glasses were cleaned by sonication in acetone, deionized water, and isopropanol, and finally UV-ozone treating for 30\\u00a0min. Different CBLs were spin coated onto the ITO glasses and followed by annealing in N2 glove box at 120\\u00a0\\u00b0C for 10\\u00a0min. For P3HT:PC61BM based inverted solar cells, the active layers (\\u223c230\\u00a0nm) composed of P3HT and PC61BM (1:1, w/w) were spin coated from a mixture solution of P3HT and PC61BM in 1,2-dichlorobenzene (o-DCB, with a total concentration of 40\\u00a0mg/mL) at 600\\u00a0rpm for 90\\u00a0s. Subsequently, the active layers were annealed at 120\\u00a0\\u00b0C for 10\\u00a0min in N2 glove box. For the PTB7-Th:PC61BM inverted solar cell, the polymer PTB7-Th and PC61BM were first dissolved in chlorobenzene with ratio of 1:1.5 (with a total concentration of 25\\u00a0mg/mL) with addition of 3% volume ratio of 1,8-diiodooctane (DIO). The active layers were spin-coated on the CBLs. On the top of photoactive layers, 20\\u00a0nm MoO3 and 100\\u00a0nm Al electrode were evaporated at pressure about 8\\u00a0\\u00d7\\u00a010\\u22125\\u00a0Pa.\\n\\nThe perovskite solar cell devices were fabricated according to the following procedure. Purchased indium-tin oxide (ITO) substrates were subsequently cleaned by ultrasonic in surfactant aqueous solution, deionized water, acetone, and isopropanol. After nitrogen blow drying, the substrates were treated with ultraviolet-ozone (UVO) for 30\\u00a0min. PEDOT:PSS aqueous was spin-coated on the ITO substrates at 3500\\u00a0rpm for 60\\u00a0s and annealed at 124\\u00a0\\u00b0C for 25\\u00a0min in glove box. Then PSS-Na aqueous solution (2\\u00a0wt%) was spin-coated on the annealed film and then baked at 140\\u00a0\\u00b0C for 5\\u00a0min in the ambient . The deposition of the other layers including perovskite layer, PC61BM, ZnO:PEI layer and the cathode electrode were finished in the N2 glovebox. In detail, a 30\\u00a0wt% CH3NH3PbI3-xClx precursor solution was prepared by dissolving CH3NH3I and PbCl2 in anhydrous DMF at a molar ratio of 3:1, and stirred at 50\\u00a0\\u00b0C for 12\\u00a0h. The precursor solution was spin-coated onto the PEDOT:PSS layer at 6000\\u00a0rpm for 60\\u00a0s and annealed at 95\\u00a0\\u00b0C for 70\\u00a0min. With the increase of annealing time, the films gradually converted from yellow to brown. After being cooled to room temperature, 20\\u00a0mg/mL PC61BM in chlorobenzene solution was spin-coated on the CH3NH3PbI3-xClx layer at 1000\\u00a0rpm for 60s, and subsequently the ZnO:PEI composite inks was spin-coated on the CH3NH3PbI3-xClx film at 1000\\u00a0rpm for 60\\u00a0s. Finally a 100\\u00a0nm Al electrode was deposited under 1\\u00a0\\u00d7\\u00a010\\u22124\\u00a0Pa via thermal evaporation through a mask to ensure an effective area of 16 and 9\\u00a0mm2.\\n\\nThe current density-voltage (J-V) measurement was carried out in nitrogen glove box with a Keithley 2400 source meter under simulated AM 1.5G solar illumination (100\\u00a0mW/cm2) . External quantum efficiencies (EQE) measurements were carried out using a home-made IPCE system consisting of a 150\\u00a0W tungsten halogen lamp (Osram 64642), a monochromator (Zolix, Omni-\\u03bb300), an optical chopper, and an I-V converter. The thermal stability of the organic solar cells was measured using a thin film solar cells automatic testing equipment (Autoannealer L-CT-220, Suzhou D&R Instruments), with devices annealed at 80\\u00a0\\u00b0C for different time. The measurement is carried out in N2 glove box. The degradation process of the un-encapsulated perovskite solar devices was monitored by a decay testing system (PVLT-G6100L, Suzhou D&R Instruments) in a glovebox (H2O\\u00a0<\\u00a010\\u00a0ppm, O2\\u00a0<\\u00a010\\u00a0ppm) under the condition of the ISOS-L-1 standard .\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | ZnO | PEI,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 95,\\n Perovskite_deposition_thermal_annealing_time: 70,\\n HTL_stack_sequence: PEDOT:PSS | PSS-Na,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 400,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 49,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The preparation of formamidine iodide (FAI) was by reacting formamidine acetate with hydroiodic acid in the round-bottom flask, and then the reactants were stirred at 0 \\u00b0C for 2 h. The light-yellow powder was gained from rotary evaporation of the solvent at about 60 \\u00b0C under reduced pressure. Then the product was purified by dissolving in methanol and collected by air pump filtration. The purification process was conducted twice to get pure FAI powder. The product was completely dried at about 60 \\u00b0C in vacuum oven.\\nOther materials were purchased from Alfa without further purification.\\n\\nFTO-coated glass was cleaned by sonication in detergent and rinsed three times with ultrapure water and ethanol. A TiO2 compact layer was coated on the FTO substrate by spray pyrolysis at 450 \\u00b0C and the precursor solution is included with 0.4 mL bis(acetylacetonate) and 0.6 mL titanium diisopropoxide in 7 mL isopropanol. TiO2 mesoporous layer was spin-coated on TiO2 compact layer with the speed of 4000 r.p.m. for 20 s, from a 30 nm TiO2 paste that is dispersed by ethanol (TiO2:ethanol = 1:5.5). Then, mesoporous TiO2 were slowly sintered from room temperature to 510 \\u00b0C for 3 h. The 1.4 M Pb2+ precursor solutions of (FAPbI3)0.85(MAPbBr3)0.15 were gained from dissolving the corresponding component powders in DMSO and DMF mixed solvent (DMSO:DMF = 1:4 by volume) with stirring at 70 \\u00b0C for 30 min. Next, the precursor solutions were spin-coated onto the mesoporous layer at firstly 1100 r.p.m. for 15 s, secondly 4600 r.p.m. for 33 s in an air flowing glovebox. About 0.2 mL of chlorobenzene was quickly dripped on the substrate after the second step for 20 s. The as-prepared film was annealed at 100 \\u00b0C for 50 min on a hotplate. The HTM solution with spiro-OMeTAD (73 mg), 4-tert-butylpyridine (29 \\u00b5L), Li+ salt (17 \\u00b5L) and cobalt(III) salt (8 \\u00b5L) in chlorobenzene was deposited onto the substrate at 3000 rpm for 20 s. At last, about 60 nm of Au were coated by thermal evaporating on the HTM layer.\\n\\nThermogravimetric analysis (TGA) was recorded on TG/DTA 7300 (SEICO INST.). The measurement was carried at rate of 10 \\u00b0C/min under a under ambient N2. Common XRD and temperature-dependent XRD patterns of the perovskite films were carried out by an X\\u2019Pert PRO (PANalytical) in the 2\\u03b8 range 5\\u201370\\u00b0 at room temperature. Absorption spectra were measured on an ultraviolet\\u2212vis (UV\\u2212vis) spectrophotometer (U-3900H, HITACHI, Japan). J\\u2013V curves and PCE were recorded by using a solar simulator (Newport, Oriel Class A, 91195A) with a source meter (Keithley 2420) at 100 mW/cm2 illumination AM 1.5G. The active area of the device was 0.09 cm2 by masking a black mask. The temperature aging tests were performed in three containers with 20, 60 and 85 \\u00b0C, respectively. The containers remained less than 10% RH and keep in dark.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 50,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 60.0; 60.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 300,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Tetrabutyl titanate, lead iodide (PbI2), hydroiodic acid (45\\u202fwt% in water), guanidine thiocyanate (GuSCN), ether, methyanol, methylamine (27\\u202fwt% in methanol), and chlorobenzene were purchased from the Sinopharm Chemical Reagent Co., Ltd. N,N-dimethyl sulfoxide (DMSO), N,N-dimethyl formamide (DMF), isopropyl alcohol (IPA), ethanol, dichloromethane, acetonitrile, acetic acid (99%), ferrocene, and tetrabutylammonium hexafluorophosphate (TBAPF6) were purchased from Aladdin chemistry Co., Ltd. Spiro-OMeTAD was purchased from Xi,an Polymer Light Technology Corp. Lithium bis(trifluoromethylsulphonyl) imide (Li-TFSI) and 4-tert-butyl-pyridine (TBP) were purchased from Aldrich. The above agents were used without further purification. F-doped tin oxide (FTO) glass substrates were purchased from the Kunshan Sunlaite New Energy Technology co., Ltd.\\nMethylammonium iodide (MAI) was prepared by stirring 20\\u202fmL methylamine and 20\\u202fmL hydroiodic acid at 0\\u202f\\u00b0C for 2\\u202fh in 40\\u202fmL methanol solvent. After stirring, the solution was spun at 50\\u202f\\u00b0C to remove excess reactant and solvent. Then the sediment was washed with ether and dried in vacuum for 24\\u202fh.\\n\\nAll the preparation processes were under air atmosphere. The etched FTO substrates (2.0\\u202fcm\\u202f\\u00d7\\u202f2.0\\u202fcm) were sequentially washed with soap water, distilled water and ethanol. TiO2 compact layer (CL) was spin-coated onto the FTO substrate at 500\\u202frpm for 9\\u202fs and 2500\\u202frpm for 30\\u202fs, then annealed at 450\\u202f\\u00b0C for 30\\u202fmin. TiO2 electron-transporting layer (ETL) was fabricated by spin-coating onto the TiO2 CL with TiO2 slurry according to previous report [26] at 500\\u202frpm for 9\\u202fs and 2500\\u202frpm for 30\\u202fs, followed by annealing at 450\\u202f\\u00b0C for 30\\u202fmin.\\nThe perovskite layer was prepared by the two-step sequential deposition in the air. First, 1.00\\u202fM PbI2 precursor solution with a different mass fraction of 0%, 1.00%, 2.00%, 3.00% GuSCN in a mixed solvent of DMF and DMSO with a volume ratio of 7: 3 was spin-coated onto the TiO2 ETL at 500\\u202frpm for 6\\u202fs and 2000\\u202frpm for 30\\u202fs, then annealed on a hotplate at 100\\u202f\\u00b0C for 10\\u202fmin. After cooling, 0.06\\u202fM MAI in IPA was infiltrated for 1\\u202fmin onto PbI2 film and spin-coated at 2000\\u202frpm for 10\\u202fs. Finally, in order to obtained higher quality perovskite film, we used post-treatment method [20]. The post-treatment solution without or with 0.20% DMSO (volume fraction) in IPA was spin-coated at 2000\\u202frpm for 10\\u202fs and annealed at 100\\u202f\\u00b0C for another 10\\u202fmin. Among them, the perovskite films fabricated without DMSO post-treatment but with adding different mass fraction of 0%, 1.00%, 2.00%, 3.00% GuSCN were defined as a, b-1, b-2, b-3, respectively. The perovskite film with 0.20% DMSO post-treatment and with 2.00% GuSCN was defined as c.\\nThe Spiro-OMeTAD solution hole-transporting layer (HTL) was spin-coated onto the perovskite layer at 500\\u202frpm for 6\\u202fs and 2000\\u202frpm for 30\\u202fs. The HTL solution was received by dissolving the 73\\u202fmg Spiro-OMeTAD and 46.0\\u202f\\u03bcL lithium solution into 1\\u202fmL chlorobenzene. The lithium solution was prepared by dissolving the 11.24\\u202fmg Li-TFSI into 33.5\\u202f\\u03bcL TBP and 21.5\\u202f\\u03bcL acetonitrile.\\nLastly, 200\\u202fnm Ag electrode was deposited onto the HTL by vacuum evaporation method.\\n\\nFourier transform infrared (FTIR) spectra were measured by using FTIR spectrometer (BRUKER TENSOR 27). The sample composition was recorded on a X-ray power diffraction (BRUKER D8-ADVANCE). The surface and cross-sectional character of samples was displayed on a field emission scanning electron microscopy (FESEM, JEOL-JSM-6701F) with the operating voltage at 10\\u202fkV. Agilent 8453 ultraviolet to visible (UV\\u2013Vis) diode array spectrophotometer was used to record the UV\\u2013Vis absorption spectra of perovskite layer. The energy level of the perovskite layer was tested by the cyclic voltammetry (CV) using CHI660D in 0.10\\u202fM dichloromethane solution of TBAPF6. Ferrocene was used as reference for calibration. The Ag/AgCl electrode, FTO glass with perovskite layer, and platinum wire were used as the reference electrode, working electrode, and counter electrode, respectively. Edinburgh Instrument FLS980 was used to perform the steady-state photoluminescence (PL) curves. The photocurrent density-voltage (J-V) characteristic curves and stability of devices were measured using a computer-controlled CHI660D. Zennium CIMPS-pcs2 (Zahner) system by the tunable light source (TLS03) was employed to perform the incident monochromatic photon-to-current conversion efficiency (IPCE) of PSC.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 168,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 79.56,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: TRUE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium bromide (MABr) was synthesized by reacting 29 mL of methylamine (40% in methanol, TCI) with 100 mL of hydrobromic acid (48 wt% in water, Aldrich) in a 250 mL round bottom flask at 0 \\u00b0C for 2 hours with stirring. The solvent was removed in a rotary evaporator at 50 \\u00b0C for 1 hour and the precipitate was collected. The precipitate was filtered and washed with diethyl ether repeatedly three times, and the white solid was collected and dried at 60 \\u00b0C in a vacuum oven for 24 h.\\nBenzyl ammonium bromide (BABr)/phenylethyl ammonium bromide (PEABr)/propylphenylammonium bromide (PPABr) was synthesized by dropwise addition of hydrobromic acid (48 wt% in water, Aldrich) in excess to a stirred solution of 10 mL of phenylethyl ammonium dissolved in 10 mL of absolute ethanol at 0 \\u00b0C. After the addition of the acid, the precipitate was left for 20 minutes at the same temperature. The precipitate was then washed repeatedly three times with diethyl ether and recrystallized twice with absolute ethanol.\\nThe perovskite solutions were prepared by dissolving stoichiometric quantities of components according to the molecular formula (R)2(MA)n\\u22121PbnBr3n+1 in a 1:1 ratio of \\u03b3-butyrolactone (GBL):dimethyl sulfoxide (DMSO), at 2 M concentration.\\n\\nThe TiO2 nanoparticles (20 nm, dyesol) were diluted in a 1:4 ratio in ethanol and spin-coated (5000 rpm, 30 seconds) onto a substrate with the architecture of SnO2:F(FTO) conductive glass (15 O cm1, Pilkington) coated by a layer of compact TiO2 (TiDIP, 75% in isopropanol, Aldrich). The substrate was then treated with TiCl4. Perovskite solutions were dropped onto the substrate and spin coated at 1000 rpm for 10 seconds followed by an additional spin of 5000 rpm for 60 seconds; during the second spin 40 \\u03bcL of toluene was added dropwise onto the substrate. The films were annealed at 100 \\u00b0C for 1 hour.\\nFor the HTM-fabricated cells, 40 \\u03bcL of 0.06 M 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenyl amino)-9,9\\u2032-spirofluorine (spiro-OMeTAD) in chlorobenzene with additives of 26.2 \\u03bcL/1 mL bis(trifluoromethane)sulfonimide lithium salt in acetonitrile (520 mg mL\\u22121), 29.0 \\u03bcL/1 mL tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)-cobalt(III) tris(bis(trifluoromethylsulfonyl)imide) in acetonitrile (300 mg mL\\u22121), and 19.2 \\u03bcL/1 mL of 4-tert-butylpyridine (Aldrich) was spin coated at 4000 rpm for 30 s.\\nThen, a 70 nm-thick gold electrode was thermally evaporated on the film under a vacuum of \\u223c10\\u22127 Torr.\\nAbsorption measurements. Absorption measurements were performed using a Jasco V-670 spectrophotometer.\\nContact angle measurements. Contact angles were collected using a Rame-Hart 100 goniometer (Rame-Hart Instrument Co., Succasunna, NJ, USA).\\nPhotovoltaic characterization. Photovoltaic measurements were performed on a New Port system, composed of an Oriel I\\u2013V test station using an Oriel Sol3A simulator. The solar simulator is class AAA for spectral performance, uniformity of irradiance, and temporal stability. The solar simulator is equipped with a 450 W xenon lamp. The output power is adjusted to match AM1.5 global sunlight (100 mW cm2). The spectral match classifications are IEC60904-9 2007, JIC C 8912, and ASTM E927-05. I\\u2013V curves were obtained by applying an external bias to the cell and measuring the generated photocurrent with a Keithley model 2400 digital source meter.\\nX-ray diffraction. X-ray diffraction measurements were performed on a D8 Advance diffractometer (Bruker AXS, Karlsruhe, Germany) with a secondary graphite monochromator, 2\\u00b0 Soller slits, and a 0.2 mm receiving slit. XRD patterns ranging from 2\\u00b0 to 75\\u00b0 2q were recorded at room temperature using Cu K\\u03b1 radiation (l = 1.5418 \\u00c5) with the following measurement conditions: a tube voltage of 40 kV, a tube current of 40 mA, a step-scan mode with a step size of 0.02\\u00b0 2\\u03b8, and a counting time of 1 s per step.\\nOriel IQE-200. An Oriel IQE-200 was used to determine the monochromatic incident photon\\u2013electric current conversion efficiency. Under full computer control, light from a 150 W xenon arc lamp was focused through a monochromator in the 300\\u20131800 nm wavelength range onto the photovoltaic cell being tested. The monochromator was incremented through the visible spectrum to generate the IPCE (\\u03bb), as defined by IPCE (\\u03bb) = 12400 (Jsc/\\u03bb\\u03d5), where l is the wavelength, Jsc is the short-circuit photocurrent density (mA cm2), and \\u03d5 is the incident radiative flux (mW cm2). Photovoltaic performance was measured by using a metal mask with an aperture area of 0.04 cm2.\\nCharge extraction measurements. Charge extraction measurements were performed using an Autolab Potentiostat-Galvanostat (PGSTAT) with a FRA32M LED driver equipped with a white light source. The cells were illuminated from the substrate side. The Nova 1.11 software program was used to collect and analyze the obtained data. A typical charge extraction experiment consisted of (1) a two-second step in which the cell is discharged in the dark. (2) The cell is then disconnected and illuminated for 2 seconds (illumination time). (3) The light is then switched off and the system waits for a certain time called the delay time. In this step, a charge is recombined inside the cell. (4) The cell is then reconnected and the charges that were left and did not recombine are extracted and measured. This process is repeated for different delay times, ranging from 0.5 seconds to 15 seconds. The charges collected are plotted against the delay time to give insight into the life-span of the charges after a certain delay time.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: TiCl4,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbBr3,\\n Perovskite_composition_short_form: MAPbBr,\\n Perovskite_additives_compounds: BA,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"By changing the reaction conditions from sonication at room temperature to reflux, the formation ratio of the \\u03b1-DMEC70 with respect to the other two isomers (Fig. 1a) was improved from 82% to 90% (Scheme S1\\u2020). C70 (84 mg, 0.10 mmol) was dissolved in chlorobenzene (30 mL) under sonication for 5 min, and then DIB (200 mg, 0.62 mmol), glycine methyl ester hydrochloride (100 mg, 0.79 mmol) and sodium carbonate decahydrate (100 mg, 0.35 mmol) were added. The flask was wrapped with aluminum foil and refluxed for 30 min. The solution was directly poured onto a silica gel column and CS2 was used to separate the unreacted C70, and DMEC70 was purified using a toluene/ethyl acetate (9:1) mixture. The regioisomeric yield was 85%. The ratio of the mono-adducts in the mixture was 90:5:5 (\\u03b1:\\u03b2-endo:\\u03b2-exo) as determined by 1H NMR and the molecular mass was determined by matrix assisted laser desorption/ionization-time-of-flight-mass spectrometry (MALDI-TOF-MS) (Fig. S1\\u2020).\\n\\nMethylammonium iodide (CH3NH3I) was prepared using a previously reported procedure. PSCs with a configuration of ITO/PEDOT:PSS/perovskite/fullerene derivative/Al were fabricated on ITO-coated glass substrates with a resistivity of 10 \\u03a9 cm\\u22122. The patterned ITO glass substrates were cleaned sequentially with detergent, deionized water, isopropyl alcohol and acetone, each step for 30 min, and then dried with nitrogen gas and finally treated in a UV-ozone oven for 30 min. After passing through a 0.45 \\u03bcm PVDF filter, the PEDOT:PSS solution (Baytron P VP AI 4083) was spin-coated onto the treated ITO substrates at 5000 rpm for 30 s, and heated at 150 \\u00b0C for 15 min in air. Then the substrates were transferred to a N2-filled glovebox where CH3NH3PbI3 (1 M solution in DMF) was spin-coated on top of the PEDOT:PSS coated substrates at 800 rpm for 10 s and at 4000 rpm for 25 s, 80 \\u03bcL of toluene were added 5 s after the second step and then the devices were annealed at 70 \\u00b0C for 60 min and the fullerene derivatives dissolved in chlorobenzene (20 mg mL\\u22121) were spin-coated onto the CH3NH3PbI3 layer at 5000 rpm for 30 s. Finally, aluminum electrodes (100 nm) were deposited by thermal evaporation under a pressure of 1 \\u00d7 10\\u22126 Torr through a shadow mask. The active area of the fabricated devices was 6 mm2. The top aluminum electrodes were encapsulated with a UV-curable epoxy resin and a glass slide before testing.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: a-DMEC70,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 240,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 60,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"ITO-coated glass substrates (Merck) were patterned using 2 M HCl, cleaned through ultrasonication (20 min each) with detergent, de-ionized water, acetone, and isopropyl alcohol, and then dried in an oven for 1 h. The materials for the HTLs and ETLs were PEDOT:PSS (CleviosTM P VP AI 4083) and PC61BM (FEM Technology), respectively. The perovskite active layers were made from the precursor I201 (Ossila) containing MAI:PbI2:PbCl2 at 40 wt% (stoichiometry of 4:1:1) in anhydrous N,N-dimethylformamide (DMF). The small-molecule additive Bphen was obtained from Sigma-Aldrich; monolayer MoS2 powder was purchased from Ossila. The solutions for the ETL were prepared by dissolving PC61BM (20 mg mL\\u22121) and Bphen at certain ratios in chlorobenzene, then stirring continuously in a N2-filled glove box for 12 h at 85 \\u00b0C prior use. The solutions for the HTL [MoS2 (1 mg) in PEDOT:PSS solution (1 mL)] were dispersed through ultrasonic oscillation for 1.5 h.\\n\\nThe patterned ITO glass substrates were treated with UV ozone for 15 min prior to use; the HTL solution was then spin-coated (4000 rpm, 40 s) onto the ITO substrates. The ITO/HTL films were baked at 150 \\u00b0C for 15 min under the atmosphere. The HTLs containing MoS2 were treated with UV ozone for 20 min before the films were transferred to a N2-filled glove box. The perovskite ink was heated at 70 \\u00b0C for 1 h, cooled to room temperature, and deposited through spin-coating (4000 rpm, 30 s) onto the ITO/HTL surface. The films were then annealed at 90 \\u00b0C for 50 min. The solutions for the ETL were passed through a PTFE filter (0.2 \\u03bcm) and then spin-coated (1200 rpm, 30 s) onto the ITO/HTL/CH3NH3PbI3\\u2212xClx surfaces. Device fabrication was completed through thermal evaporation of a 100 nm-thick film of Ag as the cathode under high vacuum (pressure: ca. 5 \\u00d7 10\\u22127 mbar). During the thermal evaporation process, a shadow mask was used to define a device area of 0.1 cm2.\\n\\nCurrent density\\u2013voltage (J\\u2013V) characteristics were recorded using a Keithley 2400 source-measure unit. A solar simulator, comprising a Xe lamp-based 150 W solar simulator (Newport 66902) and an AM 1.5G filter, was used to give an irradiance of 100 mW cm\\u22122 on the surface of the solar cell. A calibrated mono-silicon diode equipped with a KG-5 filter, exhibiting a response in the range 300\\u2013800 nm, was used as a reference. External quantum efficiency (EQE) data were obtained using an EQE-D-3011 system (Enlitech, Taiwan) and a calibrated mono-silicon diode as a reference (displaying a response from 350 to 800 nm). Sample films were prepared by spin-coating the ETL and HTL solutions onto either 4 cm2 quartz (for UV-Vis spectroscopy) or a 2.25 cm2 silicon wafer (for UPS); PEDOT:PSS/CH3NH3PbI3\\u2212xClx/PC61BM:Bphen structures on a silicon wafer were prepared for GISAXS analyses. UV-Vis absorbance spectra were recorded using a Hitachi U-4100 spectrophotometer equipped with an integrating sphere, steady-state PL spectra were recorded in air using a Hitachi F-7000 fluorescence spectrophotometer; time-resolved PL spectra were collected in a customized single photon counting system which contains a sub-nanosecond pulsed diode laser (\\u03bb = 320 nm, PicoQuant, PLS 320), a grating spectrometer and a high-speed photomultiplier tube with the single photon counting card. Film morphologies were recorded using an atomic force microscope (Veeco Innova) operated in tapping mode. A JEOL-2010 transmission electron microscope was used to record images at a beam energy of 200 keV. UPS was performed at a sample bias of 4 V by He irradiation. Synchrotron GISAXS analysis [X-ray beam energy: 10 keV (\\u03bb = 1.24 \\u00c5); incident angle: 0.15\\u00b0] was performed at the BL23A SWAXS beam line in the NSRRC, Hsinchu, Taiwan.\\n\\nElectron- and hole-only devices were prepared having the structures ITO/ZnO/ETL(PC61BM:Bphen)/Ag and ITO/HTL(PEDOT:PSS:MoS2)/Ag, respectively. The charge carrier mobility was determined using the single carrier SCLC model, as described by the Mott\\u2013Gurney law,\\nwhere J is the current density, \\u03b50\\u03b5r is the dielectric permittivity of the ETL or HTL; L is the thickness of the ETL or HTL; \\u03bc is the zero-field mobility; and V is the internal voltage in the device, given by\\nwhere Vappl is the applied voltage, Vrs is the voltage drop resulting from the relative difference in work function, and Vbi is the built-in voltage resulting from the relative difference in work function between the two electrodes.\\n\\nTime-resolved pump-probe studies were performed using a femtosecond Ti:sapphire laser system (Legend-USP-HP, Coherent) delivering a near-infrared (NIR) pulse (duration: ca. 40 fs; repetition rate: 5 kHz; center wavelength: 800 nm). The NIR laser pulse was split into two NIR pulses, with a power ratio of 10:1, using a beam splitter. The higher-intensity NIR pulse was focused into a \\u03b2-barium borate crystal for second harmonic (SH) generation; the generated SH laser pulse was guided to a delay stage for retro reflection, and then focused onto the sample as a pump pulse. The lower-intensity NIR pulse (pulse energy: 5 \\u03bcJ) was focused onto a sapphire plate (thickness: 2 mm) to generate a white light continuum (WLC); the WLC pulse was focused onto the sample as a WLC probe pulse. Using a parabolic mirror, both the pump (400 nm) and WLC probe (500\\u2013750 nm) pulses were focused onto the sample. A charge-coupled device camera (Series 2000, Entwicklungsburo Stresing), connected through an optical fiber and polychromator (CP140, Yobin Yvon), recorded the probe pulse transmitted through the sample. For measurements of the change in absorption with and without sample excitation, the pump frequency was modulated with an optical chopper running at 2.5 kHz. The difference absorption spectrum (\\u0394A) of the sample at each time delay between the pump and probe pulses was acquired using LabVIEW software. The delay was scanned using a delay stage inserted in the optical path of the pump pulses.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Bphen,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 50,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: MoS2,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Urea and thiourea were purchased from Sinopharm Chemical Reagent Co. Ltd., PbI2, bis(trifluoromethane)sulfonimide lithium salt (LiTFSI) and PbBr2 were from Aldrich, methyl ammonium iodide (MAI), methyl ammonium bromide (MABr) and formamidinium iodide (FAI) were from Shanghai Materwin New Materials Co. Ltd., N,N-dimethylformamide (DMF), dimethyl sulphoxide (DMSO), acetonitrile and chlorobenzene were from Alfar Aesar, spiro-OMeTAD was from Luminescence Technology Corp., Taiwan. The TiO2 slurry (Dyesol 30 NR-D) for mesoporous scaffolds was from Dyesol. All the chemicals were directly used without further purification. Spiro-OMeTAD chlorobenzene solution was prepared according to the literature. The electrode substrates were fluorine-doped tin oxide conducting glass (FTO, thickness: 2.2 mm, Pilkington, sheet resistance: 14 \\u03a9 per square). Before use, the FTO glass was first laser-patterned, then cleaned with a mild detergent, rinsed with distilled water several times and subsequently with ethanol in an ultrasonic bath, and finally dried under an air stream.\\n\\nAl2O3 substrates for PL measurement were prepared via 100 deposition cycles on the glass substrate by Atomic Layer Deposition (ALD). A compact TiO2 layer was obtained by spin-coating an n-butyl alcoholic solution containing 0.125 M titanium isopropoxide and HCl on the FTO glass, followed by sintering at 500 \\u00b0C for 60 min. A 150 nm-thick mesoporous TiO2 layer was further deposited on the top of the compact TiO2 layer by spin-coating a 30 nm-sized TiO2 nanoparticle dispersed solution in ethanol, and then sintered at 500 \\u00b0C for 30 min. TiO2 films were further treated with aqueous TiCl4 solution (25 mM) at 70 \\u00b0C for 15 min, followed by spin-coating acetonitrile solution of LiTFSI (0.1 M), and finally sintered at 500 \\u00b0C for 30 min.\\nPerovskite precursors were prepared by dissolving 1.32 M PbI2, 0.12 M PbBr2, 1.08 M FAI, 0.24 M MAI, 0.12 M MABr and different Lewis bases in DMF. The mixed perovskite was described as (FAPbI3)0.75(MAPbI3)0.17(MAPbBr3)0.08. A total of six precursor solutions were involved. The precursor solution with DMSO was prepared by dissolving the mixture in 0.8 mL DMF and 0.2 mL DMSO, the precursor solution with urea or thiourea was prepared by dissolving the mixture and 1.44 M urea or thiourea in 1 mL DMF, and the precursor with a mixed Lewis base of DMSO and urea (or thiourea) (defined as DMSO/urea and DMSO/thiourea, respectively) was prepared by dissolving the mixture and 5% molar ratio of urea or thiourea in 0.8 mL DMF and 0.2 mL DMSO. For comparison, the precursor without the Lewis base was also prepared by dissolving the mixture in 1 mL DMF.\\nPerovskite films were prepared by spin-coating precursors with DMSO, DMSO/urea and DMSO/thiourea on the top of mesoporous TiO2 films first at 1000 rpm for 10 s and then 5000 rpm for 30 s. During the second step, 120 \\u03bcL chlorobenzene was dropped after 15 s to remove extra DMF/DMSO and facilitate the perovskite crystal growth. For the precursors with urea or thiourea or without the Lewis base, the film fabrication processes were the same as the above except for 100 \\u03bcL chlorobenzene was dropped on the substrate after 6 s. Perovskite films for devices and PL measurement were heated at 150 \\u00b0C for 10 min and then at 100 \\u00b0C for 40 min. A 200 nm-thick spiro-OMeTAD layer was deposited on the surface of the perovskite layer by following the literature. Finally, an 80 nm-thick Au photocathode was deposited by thermal evaporation under a vacuum of 10\\u22127 Torr. Perovskite films for the ripening test were heated at 100 \\u00b0C for 1, 10 or 40 min. The samples for the Lewis base post-treatment test were first heated at 100 \\u00b0C for 10 min and cooled down, then spin-coated with isopropanolic solutions of urea or thiourea (5 mg mL\\u22121) and finally annealed for 30 min. All the precursor preparation and spin-coating processes were carried out in a glovebox.\\n\\nScanning electron microscopy (SEM) images were obtained on a Hitachi S-4800. X-ray diffraction (XRD) measurement was carried out on a Bruker X-ray diffractometer using CuK\\u03b1 as the radiation source. Fourier Transform Infrared (FT-IR) spectra were measured on a Bruker TENSOR 27. Time-resolved transient photoluminescence (PL) spectra were measured on a PL spectrometer, FLS 900, Edinburgh Instruments, excited by a picosecond pulsed diode laser (EPL-640) with a wavelength of 638.2 nm and measured at 775 nm after excitation. Carrier lifetimes were estimated by fitting PL curves with a bi-exponential decay model. Photocurrent\\u2013voltage characteristics (I\\u2013V) were measured on a Keithley 2602 SourceMeter under AM 1.5 irradiation (100 mW cm\\u22122) from an Oriel Solar Simulator 91192. Devices are masked with a black mask to define the active area of 0.1 cm2. Reverse scan J\\u2013V curves (from the open circuit to the short circuit) are adopted here with a scan speed of 30 mV s\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | Li-TFSI; TiCl4,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.75MA0.25PbBr0.24I2.76,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: Urea,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150.0; 100.0,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 40.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (CH3NH3I, \\u226599.5%, 4 times purified) was purchased from Xi'an Polymer Light Technology Corp. N,N-Dimethylformamide (DMF, 99.8%), 4-tert-butylpyridine (tBP, 96%), lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI, 99.95%) and chlorobenzene (C6H5Cl, anhydrous, 99.8%) were purchased from Sigma-Aldrich. Acetonitrile (CH3CN, 99.8+%, Argon), lead(II) iodide (PbI2, 99.9985%) and cuprous iodide (CuI, 99%) were purchased from Alfa Aesar. Spiro-OMeTAD was purchased from LumTec. Diphenyl ether (C12H10O, >99%), oleylamine (OLA, 80\\u201390%), N,N\\u2032-diphenylthiourea (C13H12N2S, 98%), antimony trichloride (SbCl3, 99%) and 1-hexanethiol (C6H14S, 96%) were purchased from Aladdin. Hexane, methanol and TiCl4 were purchased from Sinopharm Chemical Reagent Co., Ltd in China.\\n\\nA hot-injection method was applied to prepare the Cu12Sb4S13 QDs, and the detailed synthesis process was described in our previous work. The product was purified by a precipitation/dispersion cycle: the mother liquor (1 mL) was added into methanol (3 mL) and the precipitates were separated by centrifuging at 8000 rpm for 3 min. Hexane (5 mL) was used to re-disperse the QDs, and the dissolved solution was centrifuged again at 8000 rpm for 3 min to obtain the liquid supernatant for the follow-up work. The product was further purified by a precipitation/dispersion cycle and re-dispersed in hexanethiol before being employed as the precursor solution of HTMs. In our case, it was found that the metal salt could not coordinate well with oleylamine when the reaction temperature was below 110 \\u00b0C, while the stability of the QD solution became worse when the reaction temperature was higher than 150 \\u00b0C. Therefore, the reaction temperatures were controlled as 110 \\u00b0C, 130 \\u00b0C and 150 \\u00b0C.\\n\\nThe etched FTO glasses were cleaned by ultrasound for 15 min with detergent, deionized water and ethanol in sequence. Next, the cleaned FTO glasses were used as substrates to deposit an ultrathin TiO2 film, which was prepared by hydrolysis of 50 mM TiCl4 solution at 70 \\u00b0C for 1 h. After being washed with deionized water, the substrates were annealed on a hotplate at 450 \\u00b0C for 10 min. The above fabrication process of the TiO2 film was repeated again to deposit a compact TiO2 film. To prepare the perovskite layer, 231.4 mg PbI2 and 80 mg CH3NH3I3 were dissolved in 0.5 mL DMF to form a 1 M perovskite precursor solution and shaken in a spiral mixer for 10 min to form a homogeneous and clear yellow solution. An anti-solvent method was used to prepare a smooth, pinhole-free and high quality perovskite film. The perovskite precursor solution was spin-coated on the TiO2 film at 5000 rpm for 30 s with chlorobenzene as an anti-solvent after plasma pre-treatment for 120 s. Then, the prepared perovskite layer was annealed at 100 \\u00b0C for 10 min, and the film color turned from yellow to dark. In particular, to obtain a larger perovskite crystal, the traces of Pb(SCN)2 were added into the perovskite precursor solution. Thereafter, the QD solution dispersed in hexane was centrifuged at 8000 rpm for 3 min again, and the precipitate was redispersed in hexanethiol to form the precursor solution of QDs. Then the precursor solution of QDs was spin-coated onto the perovskite layer at 4000 rpm for 30 s to form an ultrathin QD film. To optimize the thickness of the QD layer, the concentration of the QD solution and the thickness of the deposited QD layer were controlled in the ranges of 5\\u201315 mg mL\\u22121 and 1\\u20133 layers, respectively. The formed QD layer was annealed at 110 \\u00b0C for 3 min. For comparison, a spiro-OMeTAD precursor solution consisting of 41.6 mg spiro-OMeTAD, 7.81 \\u03bcL LiTFSI, 16.88 \\u03bcL tBP and 0.5 mL chlorobenzene was prepared after being shaken for 5 min. Subsequently, the spiro-OMeTAD solution was spin-coated on the perovskite layer at 3000 rpm for 30 s. Finally, the counter electrode Au was thermally evaporated on HTLs with a thickness of 80 nm. The preparations of the perovskite, QDs and spiro-OMeTAD were conducted in a glovebox filled with high purity argon to prevent the deterioration of the perovskite.\\n\\nThe crystal structures and microstructures of the as-prepared QDs were characterized using an X-ray diffractometer (XRD, Pert-Pro, PANalytical, Netherlands) and a High-Resolution Transmission Electron Microscope (HRTEM, JEM-2100F, JEOL, Japan). UV-vis absorption (UV-2550, Shimadzu, Japan) in the wavelength range from 300 nm to 800 nm was recorded to characterize the optical absorption properties of the samples. A Field Emission Scanning Electron Microscope (FESEM, JSEM-5610LV, Hitachi, Japan) was used to observe the morphology of the materials and PSCs. Electrochemical Impedance Spectra (EIS) (Autolab Potentiostat 30, PGSTAT100, Netherlands) and steady-state PL spectra (LabRam HR, HORIBA Jobin Yvon, France) were taken to evaluate the hole mobility of QDs in PSCs, and the films for steady-state PL measurements were deposited on glass substrates and measured from the glass side. Ultraviolet Photoelectron Spectroscopy (UPS, ESCALAB 250Xi, Thermo Fisher, USA) measurements were made using He I radiation (21.2 eV) and the samples were drop-cast on copper sheets.\\nBesides, the power conversion efficiency was examined using current density\\u2013voltage (J\\u2013V) measurements to test the photovoltaic performances of the prepared devices. J\\u2013V curves were obtained with a voltage setting from \\u22121.5 V to 0.5 V using a Keithley Model 2430 under AM 1.5G simulated irradiation with a standard solar simulator (Model 91160-1000, Newport, USA). The light intensity of the solar simulator was calibrated using a light irradiation meter (Model 91150V, Newport, USA). The PSCs were masked with a definite aperture to define an active area of 0.25 cm2. Incident Photo-to-current Conversion Efficiency (IPCE) spectra were collected with a solar simulator (74004-1, 300 W xenon lamp, Newport, USA) coupled with a power meter (Model 2396R, Newport, USA) and an aligned monochromator (Oriel Cornerstone 130 1/8 m, Newport, USA). The photo-generated current was evaluated after calibrating the lamp spectrum with an UV-enhanced Si photodetector (Newport). The femtosecond laser transient absorption spectroscopy (TAS, Spirit 1040-8-SHG, Spectra-Physics, USA) measurements were taken to investigate the carrier transport process at the interfaces between the perovskite film and HTMs.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Pb(SCN)2,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.25,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"C60 (99.9%) and C70 (99%) were purchased from Puyang Yongxin Fullerene Technology Co., Ltd. and used without further purification. H2O2 (30 wt%) and NH4OH (25\\u201328 wt%) were purchased from Aladdin Industrial Corporation. Ethanol was purchased from Chinasun Specialty Products Co., Ltd.\\nMethylammonium iodide (MAI) was synthesized following the procedures in the literature. Methylammonium chloride (MACl) and PbI2 (99.999%) were purchased from Xi'an Polymer Light Technology Corp and Alfa Aesar, respectively.\\n\\nAll the perovskite solar cells were fabricated on ITO-coated glass substrates (10 \\u03a9 sq\\u22121, CSG Holding Co., Ltd.). The ITO substrates were cleaned in an ultrasonic bath using detergent, water, deionized water, acetone, ethanol and isopropanol for 20 min each. To obtain a hydrophilic surface, the ITO slides were treated with UVO for 20 min after being dried in a nitrogen flow. The fullerene derivatives f-C60 and f-C70 were dissolved in ultrapure water with different concentrations, and the f-C60 and f-C70 solutions were spin-coated on top of the ITO substrate at 1500 rpm for 60 s. After being annealed at 120 \\u00b0C for 25 min, the slides were transferred to obtain the C60 layer by vacuum evaporation. The thickness of the C60 layer was controlled to 12 nm.\\nThe perovskite film was deposited by a new solvent-assisted molecule inserting strategy (S-AMI) method. PbI2 was dissolved in N,N-dimethylformamide (DMF, 99.8%, J&K) with a concentration of 461 mg mL\\u22121, and MAI and MACl were dissolved in isopropanol (IPA, J&K) with a mass ratio of 10:1 (MAI, 50 mg mL\\u22121). All the perovskite precursor solutions were stirred at 70 \\u00b0C overnight and filtered using a 0.22 \\u03bcm PTFE filter before use. The PbI2 solution was spin-coated on the substrate at 4500 rpm for 20 s and then the MAI and MACl solution was dropped onto the center of the wet spin-coating PbI2 film for 25 s. After putting the samples on a hot plate, the film color turned dark brown immediately, and the perovskite film was annealed at 100 \\u00b0C for 7 min.\\nFor the hole transport material (HTM), 30 mg P3HT was dissolved in 1 mL ortho-dichlorobenzene (o-DCB), 20.4 \\u03bcL of bis(trifluoromethane)sulfonamide lithium salt (Li-TFSI, 28.3 mg mL\\u22121, Sigma-Aldrich) in acetonitrile and 10.2 \\u03bcL of 4-tert-butylpyridine (tBP, Sigma-Aldrich) were mixed into a P3HT solution. The P3HT layer was prepared by spin-coating onto the perovskite layer at 1200 rpm for 60 s. Finally, 7 nm of MoO3 and 100 nm of Ag were deposited under vacuum evaporation. An active area of 0.0757 cm2 of the device has been defined by using a shadow mask. The direct current conductivity was measured with a device configuration of ITO/f-C60 or f-C70/C60/Au. The Au electrode with 80 nm was evaporated under high vacuum (\\u223c10\\u22124 Pa).\\n\\nXPS was performed using an ESCALAB 250Xi (USA). The UV-vis absorption spectra of C60, C70, and f-C60 as well as f-C70 were collected on an Agilent Cary 5000 (USA). Elemental analysis was performed using an Elementar Vario EL-III instrument. FTIR and WF measurements of f-C60 and f-C70 were conducted on a VERTEX 70V (Bruker, Germany) and using peak force Kelvin probe force microscopy (KPFM), respectively. TGA was carried out on a Perkin-Elmer Pyris 6, with a heating rate of 10 \\u00b0C min\\u22121 under nitrogen flow. The J\\u2013V curves and steady-state efficiencies of Pero-SCs were acquired using a Keithley 2400 source meter under AM 1.5G illumination. A measurement system of QE-R3011 (Enli Technology Co., Ltd.) was used to measure the IPCE spectra. The thicknesses of f-C60 and f-C70 were determined using a spectroscopic ellipsometer (M-2000V, J.A. Woollam Co., USA). The SEM images were captured using an S-4700 (Japan) to study the surface morphologies. The crystallinity of the perovskite films was measured using XRD performed on a diffractometer (D2 PHASER, Bruker). AFM images were captured on a Multimode 8 microscope (Bruker, Santa Barbara, CA) in peak force quantitative nanomechanical mode. ACIS measurements were performed on an IM6 electrochemical workstation of Zahner Zennium (Germany), and Z-view software was used to analyze impedance data. An instrument of FLS980 (UK) was used to obtain steady-state PL spectra, and transient PL characterization was performed on a Lifespec II produced by Edinburgh Instrument (UK).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 7.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0757,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2, 99.999%) and tin(IV) oxide (SnO2) colloid precursor were purchased from Alfa Aesar; cesium bromide (CsBr, 99.999%), chlorobenzene (CB, 99.8%), anhydrous dimethyl sulfoxide (DMSO, \\u226599.9%), N,N-dimethylformamide (DMF, 99.8%), 4-tert-butylpyridine (tBP), tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III)-tris(bis(trifluoromethylsulfonyl) imide) (FK209) and bis(trifluoromethylsulfonyl)amine lithium salt (Li-TFSI) were purchased from Sigma Aldrich. Anhydrous methanol, ethanol (>99.5%) and isopropyl alcohol (IPA, 99.5%) were purchased from Acros; Spiro-MeOTAD (99.8%) was purchased from Xi'an Polymer Light Technology Corp. All materials and reagents were used as received without further purification.\\n\\n1 M CsBr and X M PbI2 (X = 0.95, 1.00, 1.05, 1.10) were dissolved in a mixed solvent (DMSO:DMF = 9:1) according to certain stoichiometric ratios, and stirred at 70 \\u00b0C for 12 h. The CsPbI2Br precursor solution was then obtained by filtration through a 0.22 \\u03bcm PTFE filter.\\n\\nThe ITO glasses were successively cleaned with acetone, ethanol and deionized water respectively by ultrasonic cleaning for 15 minutes, respectively. Before the spin coating, each ITO glass was blown dry with nitrogen gun and cleaned with plasma for 60 s. SnO2 was selected as the electron transport layer. We diluted the SnO2 colloid precursor to 5% with deionized water, then spin-coated at 3000 rpm for 30 s, and thermal annealed at 150 \\u00b0C for 30 min to obtain an electron transport layer. Then the 1 M CsPbI2Br precursor solution was deposited on the SnO2 layer at the speed of 1000 rpm for 10 s and 4500 rpm for 35 s in a glove box, annealing at 260 \\u00b0C for 10 minutes. For deposition of hole-transporting material, Spiro-MeOTAD was dissolved in chlorobenzene with a concentration of 80 mg mL\\u22121, then 35 \\u03bcL of lithium bis (trifluoromethanesulfonyl)imide in acetonitrile (260 mg mL\\u22121) and 30 \\u03bcL of 4-tert-butylpyridine was added into the Spiro-MeOTAD solution. The mixture was coated onto the perovskite film at 3500 RPM for 30 s to form a Spiro-MeOTAD hole-transporting layer. Finally, the counter electrode was deposited by thermal evaporation of 80 nm-thick gold under a pressure of 2 \\u00d7 10\\u22126 mbar. The active area was measured to be 0.045 cm2.\\n\\nUV-vis absorption and photoluminescence (PL) spectra of thin films were recorded on a HP 8453 spectrophotometer and FLS920 spectrofluorimeter (Edinburgh Instruments), respectively. A 150 W, ozone-free xenon arc lamp was used in PL measurements. Scanning electron microscope (SEM) images were obtained by using a field emission scanning electron microscope (JEOL-7401). Thicknesses of thin films were measured by Dektak 150 surface profilometer. X-Ray Diffraction (XRD) patterns were measured by an X-ray diffractometer Bruker D8 Advance using Cu K\\u03b1 radiation source with a scan rate of 10\\u00b0 min\\u22121.\\n\\nThe J\\u2013V characteristics of PSCs were measured by a Keithley model 2400 source measure unit (Newport, Oriel AM 1.5 G, 100 mW cm\\u22122). The light intensity of 100 mW cm\\u22122 was calibrated by a silicon reference cell. The external quantum efficiency (EQE) spectra of PSCs were performed on a DSR100UV-B spectrometer with a bromine tungsten light source, a SR830 lock-in amplifier and a calibrated Si detector.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBrI2,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: CsBr,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 260,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.045,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The materials used in this study were purchased from commercial sources and used as received. Lead iodide (PbI2, 99.9985%), cesium iodide (CsI), CsBr, SnO2 (15 wt% in an H2O colloidal dispersion), poly(3-hexylthiophene-2,5-diyl) (P3HT), and LiCl were purchased from Alfa Aesar. N,N-Dimethylformamide (DMF; 99%) and dimethyl sulfoxide (DMSO; 99.9%) were purchased from Samchun Chemicals, and chlorobenzene (99.8%) was purchased from Kanto Chemical. The CsPbI3 perovskite precursor solution was prepared by dissolving an equimolar ratio of PbI2 (0.8 M) and CsI (0.8 M) in a mixed solvent of (4:1) DMF:DMSO. The precursor solution was magnetically stirred overnight at 60 \\u00b0C and the CsBr solutions were prepared by dissolving 5, 10, or 15 mg of CsBr in methanol. Note that a concentration of CsBr greater than 15 mg was found to be insoluble in methanol at room temperature (see Fig. S1 in the ESI\\u2020). Therefore, we prepared a CsBr/methanol solution with a maximum of 15 mg of CsBr per 1 mL of methanol. A hole transport layer (HTL) was created by dissolving 10 mg of P3HT in 1 mL of chlorobenzene and stirring the solution overnight at room temperature. The P3HT solution was filtered before use. SnO2 was used as an electron transport layer (ETL) and was prepared as described in a previous report. Briefly, the SnO2 precursor solution was prepared by dissolving an SnO2 (450 \\u03bcL) colloid dispersion and an LiCl (300 \\u03bcL) aqueous solution (17 mg/4 mL) in 1.7 mL of deionized water (DI) water while stirring at room temperature for four hours.\\n\\nPlanar inorganic PSCs were fabricated with a device structure of ITO/SnO2/CsPbI3 or CsPbI3\\u2212xBrx/P3HT/Au. First, ITO substrates with a resistance of 15 \\u03a9 sq\\u22121 were sequentially cleaned using a detergent solution, DI water, acetone, and isopropanol (IPA) for 15 min each. After cleaning and drying, the substrates were treated with ozone (O3) plasma for 20 min to increase their surface wettability. The ETL was obtained by spin-coating an SnO2 precursor onto the ITO substrates at 4000 rpm for 30 s in ambient air and annealing for 170 \\u00b0C for 30 min. After cooling to room temperature, the substrates were transferred to a nitrogen-filled glovebox with air and H2O content >1 ppm for coating with the CsPbI3 perovskite layer. The CsPbI3 perovskite solution was filtered with a PVDF (0.45 \\u03bcM) filter, spin-coated onto the SnO2 layer at 2000 rpm for 45 s, and then dried for 50 min at room temperature. Following this, 100 \\u03bcL of the CsBr solutions of various concentrations were dynamically spin-coated onto the CsPbI3 film at 3000 rpm for 30 s and dried at 100 \\u00b0C for 5 min. A reference sample without CsBr treatment was annealed at 340 \\u00b0C for 8 min and the CsBr-coated samples were annealed at 300 \\u00b0C for 8 min. Fig. 1 shows the experimental process used to fabricate CsPbI3\\u2212xBrx inorganic perovskite films. The HTL layer was spin-coated onto CsPbI3 and CsPbI3\\u2212xBrx at 1500 rpm for 30 s and dried at 85 \\u00b0C for 5 min. Finally, 100 nm of Au electrodes were deposited on top of the devices using a thermal evaporator at 1.2 \\u00d7 10\\u22126 Torr after defining an effective cell area of 0.04 cm2 with a shadow mask. Note that the CsPbI3\\u2212xBrx perovskite films with various dynamic CsBr treatments \\u2013 0, 5, 10, or 15 mg \\u2013 are referred to as CsBr-0, CsBr-5, CsBr-10, and CsBr-15, respectively, for the remainder of the paper.\\nAll characterizations were carried out in an ambient atmosphere. The structural properties of the perovskite films were characterized using X-ray diffraction (XRD; R&D-100; Rigaku SmartLab). The surface and cross-sectional morphologies and the elemental mapping of the prepared films and devices were investigated using a field-emission scanning electron microscope (FE-SEM; SIGMA, Carl Zeiss). The absorption spectra of the planar perovskite films were characterized by ultraviolet-visible (UV-vis) spectrophotometry (UV-2700; Shimadzu). Steady-state PL measurements of the fabricated perovskite films were conducted using a spectrofluorometer (FP-8600, Jasco) with a laser excitation wavelength of 405 nm. All current\\u2013voltage (J\\u2013V) curves and the steady-state photocurrent of the fabricated PVSCs were measured using a solar simulator (PEC-L01, Peccell Technologies) under standard AM1.5 illumination (100 mW cm\\u22122) in atmospheric air conditions. The external quantum efficiency (EQE) spectrum was measured using a power source (Abet Technologies 150 W xenon lamp, 13014) with a monochromator (DongWoo Optron, MonoRa500i) and a CompactStat (Ivium Technologies; Eindhoven, The Netherlands) to detect responses as a function of the spectral wavelengths. Electrochemical impedance spectroscopy (EIS) measurements were carried out using an impedance analyzer (Solartron 1287) under AM1.5 illumination with an applied bias of 0.8 V for frequencies in the range 1\\u2013200 kHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: LiCl,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> Methanol,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 25 >> 100,\\n Perovskite_deposition_thermal_annealing_time: 50.0 >> 5.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 60,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless otherwise stated, all materials were purchased from Sigma-Aldrich or Alfa Aesar and used as received. Spiro-OMeTAD was purchased from Borun Chemicals and used as received. The synthesis of the perovskite CH3NH3PbI3\\u2212xClx has been reported elsewhere. TiO2 nanoparticles were synthesized following a previously reported method. In a typical synthesis 2 ml of anhydrous TiCl4 (99.9%) was added dropwise while stirring into a vial containing 8 ml of anhydrous ethanol. The whole content was transferred into a 100 ml flask containing 40 ml anhydrous benzyl alcohol. The solution was heated to 80 \\u00b0C and reacted for 9 hours. After that time the reaction was stopped by cooling down the solution, which contained a translucent dispersion of very fine TiO2 nanoparticles. Then, 4 ml of the above solution was mixed with 36 ml of diethyl ether resulting in the precipitation of the TiO2. The precipitate was centrifuged, washed with acetone and redispersed in anhydrous ethanol, resulting in a colloidal solution of approximately 28 mg TiO2/ml ethanol (3.54 wt% of TiO2). The formulation was further diluted 3 times (1.18 wt% of TiO2) in anhydrous ethanol and the appropriate amount of TiAcAc (10\\u201320 mol% with respect to the TiO2 content) was added directly. The solution was left to stand for at least 2 hours before use, but is stable for months. The low temperature TiO2 compact layer (lt-TiO2) was prepared by spin-coating the colloidal dispersion of anatase particles in anhydrous ethanol, formulated with TiAcAc, followed by drying at 150 \\u00b0C for 30 minutes. The thickness of the compact layer was tuned by the concentration of TiO2 nanoparticles (3.54\\u20130.24 wt% TiO2 to ethanol). As standard control samples, blocking layers of non-crystalline TiOx and high temperature processed TiO2 (ht-TiO2) were used. The former was prepared by spin-coating a precursor solution (titanium isopropoxide, TTIP) in anhydrous ethanol (0.254 M) with the addition of 0.02 M HCl followed by annealing at 150 \\u00b0C for 30 min, the latter was prepared by spin-coating the same solution (TTIP), followed by annealing at 150 \\u00b0C and sintering at 500 \\u00b0C.\\nPhotovoltaic devices were fabricated on fluorine-doped tin oxide (FTO) coated glass (Pilkington, TEC7). Substrates were cleaned in hallmanex, and then subjected to 10 minutes sonication in acetone, 10 minutes sonication in IPA, and 10 minutes of oxygen plasma etching. Compact layers were deposited by spin-coating, as described above. An alumina scaffold was deposited according to the previously reported method which employs Al2O3 nanoparticles of diameter <50 nm. After depositing the alumina scaffold samples were transferred into a nitrogen-filled glovebox, initially optimised precursor solution of the concentration of 350 mg ml\\u22121 (CH3NH3I and PbCl2, 3:1 molar ratio in N,N-dimethylformamide (DMF)) was spin-coated at room temperature, followed by annealing at 100 \\u00b0C for 90 minutes. The concentration of the precursor solution was re-optimised to 400 mg ml\\u22121, resulting in an increased perovskite film thickness. The hole transporter was deposited by spin-coating an 8 wt% 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-p-methoxyphenylamine)9,9-spirobifluorene (spiro-OMeTAD) in chlorobenzene with added tert-butylpyridine (tBP) and lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) of 80 and 30 mol%, with respect to spiro-OMeTAD. Finally, 150 nm thick silver electrodes were deposited on top of devices by thermal evaporation at \\u223c10\\u22126 bar, through a shadow mask.\\nUV-Vis absorption spectra were obtained using a Carry 300 Bio (Agilent Technologies) spectrometer. Scanning electron microscopy images were obtained using a Hitachi S-4300 microscope. Conductivity measurements of TiO2 films were performed by evaporating gold electrodes through the shadow mask on the spin-coated compact layers and using a 4-point probe set up with a Keithley 2400 as a sourcemeter. The electrode pattern was designed for 4-point probe measurements with an outer probe channel dimensions of 1 mm (length) \\u00d7 1 cm (width) and an inner probe separation of 300 \\u03bcm. The thickness of the channel (TiO2 layer) was determined from the SEM cross-sectional image. X-ray diffraction spectra were obtained for powder samples (the nanoparticle solution was dried in air at 150 \\u00b0C) using a Panalytical X'Pert Pro X-ray diffractometer.\\nCurrent\\u2013voltage characteristics of solar cells were measured under simulated AM1.5 100 mW cm2 sunlight (ABET Technologies Sun 2000) with a Keithley 2400 sourcemeter. The lamp was calibrated with an NREL-calibrated KG5 filtered silicon reference with a solar mismatch factor of 1.01. The active area of the device was defined by a metal mask with a square aperture of an area of 0.0625 cm2. The pre-masked active area of the solar cells was approximately 0.12 cm2 nominally defined by the overlap area of the silver and FTO electrodes. Solar cells were masked for all the current voltage measurements.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 90,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0625,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped tin oxide FTO glass substrates (Pilkington, TEC15, 15 ohm sq\\u22121) were partially etched with metallic Zn and 2 M HCl. They were washed with water and cleaned in an ultrasonic bath in acetone and isopropanol for 10 min each. Then they were immersed into a TL1 washing solution (H2O/NH3/H2O2 5:1:1, v/v) and heated to 80 \\u00b0C for 15 min to remove organic contaminants. To make a compact TiO2 blocking layer of \\u223c80 nm, the cleaned FTO glasses were coated with 0.15 M titanium diisopropoxidebis(acetylacetonate) (75% Aldrich) in 1-butanol (Aldrich) solution by spin-coating (3000 rpm), and then heated at 125 \\u00b0C for 5 min. After the coated film was cooled down to room temperature, the same process was repeated again in the same way. After the last cooling to room temperature the process was repeated with 0.3 M titanium diisopropoxidebis(acetylacetonate) solution in 1-butanol at 3000 rpm. The as-coated FTO substrates with TiO2 precursor solutions finally underwent a sintering process at 520 \\u00b0C for 2 hours. N-Dimethyloxamic acid (DMOA) and sodium phosphonoformate tribasic hexahydrate (NaPTH) were purchased from Aldrich. For functionalization, the as-prepared TiO2 substrates were immersed in 0.5 mM ethanol solution of either carboxylic or phosphonic acid for 18 h. The modified TiO2 substrates were then rinsed with ethanol, and blow-dried with nitrogen gas.\\n\\nMixed halide hybrid perovskites are prepared by self-organization processes using PbCl2 (Aldrich) and methylammonium iodide MAI precursor solutions (20 wt%) obtained by dissolving MAI and PbCl2 (3:1 molar ratio) in anhydrous N,N-dimethylformamide (DMF) at room temperature. The intermediate MAI compound was prepared by reactions of the amine, CH3NH2 (41%) (Fluka), and aqueous solutions with HI (57%, Aldrich), as previously reported. All the reagents were used as purchased without further purification.\\n\\nXPS analyses have been performed by using a PHI ESCA/SAM 5600 Multi-technique spectrometer equipped with a Mg K\\u03b1 X-ray source at a pressure of 5 \\u00d7 10\\u22129 Torr. Measurements have been performed at a take off angle (angle between the surface of the sample and the detector) of 45\\u00b0 with an angular acceptance of \\u00b15\\u00b0. The binding energy (BE) scale was calibrated by centring the C 1s signal due to the adventitious/hydrocarbon carbon at 285.0 eV.\\n\\nGIWAXS measurements were performed at the XMI-L@b with a Rigaku (GI)SAXS/(GI)WAXS laboratory set-up, equipped with a FR-E+ microsource and a SMAX3000 3-pinhole camera. The experimental settings were: 1\\u00b0 incidence angle and 0.154 nm radiation wavelength. The patterns were calibrated by using a standard Silver Behenate powder sample. Data were collected on an image plate (IP) detector with 100 \\u03bcm pixel size at 87 mm sample-to-detector distance. XRD data were collected in coupled sample-detector scan mode (\\u03b8/2\\u03b8) on a D8 Discover (Bruker) equipped with a G\\u00f6bel mirror for Cu-K\\u03b1 radiation and a scintillator detector.\\n\\nFilm absorbance spectra were measured by using a Varian Cary 5000 spectrophotometer in reflectance mode. Scanning electron microscopy (SEM) imaging was performed by using a MERLIN Zeiss SEM FEG instrument at an accelerating voltage of 5 kV using an In-lens detector.\\n\\nIn order to get an extremely ordered polycrystalline film, a warm (60 \\u00b0C) precursor solution 20 wt% MAPbI3\\u2212xClx was deposited by spin-coating on a pre-heated (120 \\u00b0C) TiO2 compact layer at 1000 rpm for 45 seconds, followed by annealing at 100 \\u00b0C for 1 h. The same procedure has been followed also for the substrates functionalized by DMOA or NaPTH functionalized TiO2. A chlorobenzene solution containing 131 mM Spiro-OMeTAD, 216 mM tert-butylpyridine and 58 mM lithium bis(trifluoromethylsulfonyl)imide salt was spin-coated onto the perovskite. Solar cell devices were completed by thermal evaporation of 200 nm Ag electrodes and left for 3 hours in ambient air. The step voltage was fixed at 10 mV and the delay time, which is a set delay at each voltage step before measuring each current, was 500 ms. I\\u2013V curves for all devices were measured by masking the active area with a black mask of 0.09 cm2 in ambient air.\\n\\nElectrochemical experiments were carried out with an Autolab Potentiostat PGSTAT 302N interfaced with a personal computer. A standard three electrode electrochemical cell with a Pt gauze counter electrode and a silver wire as the quasi-reference electrode were used. The TiO2 modified electrode with a geometric area of 1 cm2 served as the working electrode. Acetonitrile solutions with 0.1 M LiClO4 as the supporting electrolyte were used and the cyclic voltammograms were obtained at 20 mV s\\u22121. It was bubbled with Ar at least for 20 min and Ar was blown over the electrolyte during the measurement.\\n\\nTime resolved photoluminescence measurements were performed using a time-correlated single-photon counting (TCSPC) apparatus of Hamamatsu FL980, 100 ps time resolution with deconvolution analysis.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PEDOT:PSS was purchased from Heraeus (4083). Anhydrous solvents including ethanol, chlorobenzene, N,N-dimethylmethanamide, dimethyl sulfoxide and diethyl ether, as well as copper(II) chloride (CuCl2), phosphorus(V) sulfide (P2S5), 1-dodecanethiol (DDT), and oleylamine (OLA) were purchased from Sigma-Aldrich. Hexane and isopropanol (molecular biology grade) were purchased from Fisher. Methylammonium iodide and formamidinium iodide were purchased from Dyesol. Lead iodide and lead thiocyanate were purchased from Alfa Aesar. PCBM and BCP were purchased from 1-Material.\\n\\nCu3PS4 nanoparticles were synthesized according to a previous report. Briefly, a flask containing 2 mmol CuCl2, 0.5 mmol P2S5, and 4 mL DDT was heated to 250 \\u00b0C under an inert atmosphere and allowed to react for 1 h. After cooling, the contents of the flask were pipetted into a centrifuge tube for washing. Three suspension and precipitation cycles using OLA, hexane, and isopropanol were conducted, followed by three cycles using hexane and isopropanol only. The resulting NP pellet was dried under argon flow before use in device experiments.\\n\\nThe Fluorine-doped Tin Oxide (FTO) substrates were cleaned by ultra-sonication in diluted Micro-90 detergent, deionized water, acetone, and isopropanol for 30 min, respectively. A solution of Cu3PS4/chlorobenzene (30 mg mL\\u22121) was spin-coated on FTO at 4000 rpm for 50 s and annealed at 200 \\u00b0C for 120 min in N2. PEDOT:PSS films were coated on cleaned FTO substrates at 4000 rpm for 50 s and then dried at 175 \\u00b0C for 30 min in air. The perovskite precursor solution was spin-coated on the HSL layer at 500 rpm for 3 s and at 4000 rpm for 60 s using diethyl ether as the anti-solvent. After spin coating, the perovskite film was annealed at 100 \\u00b0C for 5 min. PCBM (20 mg mL\\u22121 in chlorobenzene) was then deposited on the perovskite film at 2000 rpm for 30 s and annealed at 90 \\u00b0C for 10 min. BCP (0.5 mg mL\\u22121 in ethanol) was spin-coated on the PCBM film at 4000 rpm for 30 s. A layer of 75 nm silver (Ag) was then deposited on top using thermal evaporation. The working area of the devices was 0.08 cm2 as defined by a shadow mask during Ag evaporation.\\n\\nGrazing incidence X-ray diffraction (XRD) data were obtained using a Rigaku Smartlab diffractometer (Cu K\\u03b1 source) in parallel beam geometry with an incident angle of 0.5\\u00b0. Raman spectra were collected using a 633 nm He:Ne laser coupled with a Horiba/Jobin-Yvon LabRAM HR800 confocal microscope at a magnification of 100\\u00d7. Electrochemical cyclic voltammetry (CV) was conducted on an electrochemical workstation with a Pt plate as the working electrode, a Pt slice as the counter electrode, and a Ag/AgCl electrode as the reference electrode in tetrabutylammonium hexafluorophosphate (Bu4NPF6, 0.1 M) acetonitrile solutions at a scan rate of 50 mV s\\u22121. Ferrocene/ferrocenium (Fc/Fc+) was used as the internal standard (the energy level of Fc/Fc+ is \\u22124.8 eV under vacuum), and the formal potential of Fc/Fc+ was measured to be 0.55 V vs. the Ag/AgCl electrode. The HOMO energy level was determined from the onset oxidation potential (Eoxonset) using HOMO = \\u22124.25 \\u2212 Eoxonset (eV); while the LUMO energy level was calculated from the HOMO and optical bandgap (Eg) using the formula: LUMO = HOMO + Eg (eV).\\n4.4.1. Film characterization. High resolution field emission top-view and cross-sectional SEM images of all the films and completed devices were obtained with a Hitachi S-4800 SEM. All layer thicknesses were determined using a Dektak surface profiler and the cross-sectional SEM images. TRPL measurements were conducted similarly as described in our earlier studies.\\n4.4.2. Device characterization. J\\u2013V curves were measured in air under 100 mW cm\\u22122 AM1.5G solar irradiation (PV Measurements Inc.) with a Keithley 2400 Source Meter. The incident light was controlled by a shutter. The light intensity for the J\\u2013V measurements was calibrated using a standard Si solar cell and our perovskite solar cells certified by Newport. The steady-state efficiencies were obtained by tracking the maximum output power point. EQE spectra were obtained on a QE system (PV Measurements Inc., model IVQE8-C QE system without bias voltage) using 100 Hz chopped monochromatic light ranging from 300 to 850 nm under near-dark test conditions. All characterization studies and measurements were performed in ambient atmosphere.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.3MA0.7PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1440,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Pattern fluorine doped tin oxide (FTO) (TEC15, Pilkington) substrates were cleaned by ultrasonication in an alkaline, aqueous washing solution and then rinsed with de-ionized water, ethanol and acetone. A \\u223c40nm thick blocking layer of TiO2 (Bl-TiO2) was deposited on the substrates by spin coating of 0.15 M and 0.3 M commercial titanium diisopropoxide bis(acetylacetonate) solution (75% in 2-propanol, Sigma-Aldrich) diluted in ethanol (1:39, volume ratio) as a precursor. Subsequently it was annealed in air at 450 \\u00b0C for 30 min. The TiO2 nanorods were deposited directly onto the FTO substrate using a technique reported elsewhere. Briefly, titanium(IV) isopropoxide (TTIP) was hydrolyzed in equal volumes of HCl:H2O at 180 \\u00b0C for 3 h. The films were washed several times with water/ethanol and used for further processes. The as-prepared, rutile TiO2 nanorod-coated FTO sample was further used for a secondary hydrothermal process (etching). In a typical experiment, nanorod-coated FTO substrates were immersed in an acidic solution of HCl:H2O (2:1 v:v%) and maintained at 150 \\u00b0C. The etching time was varied from 0 h (as deposited), 3.0 h, 3.5 h and 4.0 h. After completion of the etching process, the etched TiO2 nanorods were rinsed extensively with de-ionized water and dried in air. After cooling to room temperature, the substrates were treated with a 0.04 M aqueous solution of TiCl4 for 30 min at 70 \\u00b0C, rinsed with de-ionized water and dried at 500 \\u00b0C for 20 min.\\n\\nTo synthesise the TiO2 nanoflowers, titanium(IV) butoxide was hydrolyzed in an equal volume of concentrated HCl (37% Sigma Aldrich) at 180 \\u00b0C for 3 h. After TiO2 nanoflower synthesis, the samples were etched as per the method described above (for 0 h, 3.0 h, 3.5 h and 4.0 h) and used for TiCl4 treatment and then dried at 500 \\u00b0C for 20 min. Please note that fresh hydrothermal and TiCl4 treatment solutions were prepared before each experiment.\\nThe length, diameter, density and nanostructure of the TiO2 nanorods were optimized via solution concentration and etching time. The amount of TiO2 precursor (TTIP or TBT) was varied from 100 \\u03bcl to 240 \\u03bcl and the etching time was varied from 3 h to 4 h at 150 \\u00b0C, for optimization of efficiency. More details are discussed in Table S1.\\u2020\\n\\nMethylammonium lead iodide (CH3NH3PbI3) (i.e. MAPbI3) was synthesized as in previous literature. Briefly, hydroiodic acid was added dropwise to a solution of methyl-amine (aqueous, 40 wt%, TCI Chemicals) in an ice bath, and then stirred for 2 h, before the solvent was evaporated using a rotary evaporator. The resulting white solid product was dried under vacuum overnight at 50 \\u00b0C. The MAPbI3 solution was prepared by dissolving equimolar amounts of MAI and lead iodide (PbI2) in anhydrous \\u03b3-butyrolactone (GBL). The clear, filtered yellow solution was spin coated on top of the 1D or 3D TiO2 samples followed by heat treatment on a hot plate for 10 min to form dark-brown crystalline MAPbI3.\\n\\nFor the MAPbI3\\u2212xClx perovskite layer, the desired amount of MAI powder was mixed with PbI2/PbCl2 in a GBL/DMF (3:1 v/v) binary solvent and stirred at 60 \\u00b0C for 12 h. Furthermore, the formamidinium NH2CHNH2I (FAI) was first synthesized by reacting hydroiodic acid and formamidine acetate. (FAPbI3)0.85(MAPbBr3)0.15 was synthesized by reacting the desired amounts of FAI, MABr, PbI2 and PbBr2 powder in DMF/DMSO (4:1 v/v) solution. The filtered, yellow, transparent solution was spin coated on hydrothermally grown and etched TiO2 nanoflower samples. One drop of toluene or chlorobenzene was drop-cast during the second spin-coating step, followed by a heat treatment on a hot plate for 10 min to form a dark-brown, crystalline, compact, pinhole-free perovskite layer.\\nThe hole transport material (HTM) was prepared by a standard procedure reported elsewhere with a few modifications. 180 mg of 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9\\u2032-spirobifluorene (spiro-MeOTAD, Merck) was dissolved in 1 ml of chlorobenzene (99.8%, Aldrich) with the addition of 37.5 \\u03bcl of bis(trifiuoromethane) sulfonimide lithium salt (LiTFSI, 99.95%, Aldrich) (170 mg ml\\u22121) in acetonitrile and 17.5 \\u03bcl of 4-tert-butylpyridine (TBP, 96%, Aldrich). For the poly[bis(4-phenyl) (2,4,6-trimethylphenyl)amine] (PTAA)-based HTM, 15 mg of PTAA (EM Index, Mw = 17500 g mol\\u22121) in 1.5 ml of toluene was mixed with 15 \\u03bcl of LiTFSI (170 mg) in acetonitrile (1 ml) and 7.5 \\u03bcl of 4-tert-butylpyridine. The CH3NH3PbI3/TiO2 substrate was coated with a HTM solution, using the spin-coating method at 3000 rpm for 30 s. Then the substrates were transferred to a vacuum chamber and evacuated to a pressure of 2 \\u00d7 10\\u22126 mbar. For the Au counter-electrode, 80 nm thick Au contacts were deposited on the top of the HTM overlayer by thermal evaporation (growth rate of \\u223c0.5 \\u00c5 s\\u22121) at a pressure of 2 \\u00d7 10\\u22126 mbar. The active areas of all of the devices were 0.09 cm2.\\n\\nThe top-surface and cross-sectional images were recorded by a field emission scanning electron microscope (FESEM; S-4700, Hitachi). X-ray diffraction (XRD) measurements were carried out using a D/MAX Ultima III XRD spectrometer (Rigaku, Japan) with a Cu K line of 1.5410 \\u00c5. The cells were illuminated using a solar simulator at AM 1.5 G for 10 s, and the light intensity was adjusted using an NREL-calibrated Si solar cell with a KG-5 filter to 1 sun intensity (100 mW cm\\u22122). The IPCE spectra were measured as a function of wavelength from 300 to 1100 nm, using a Spectral Products DK240 monochromator. The photoluminescence (PL) spectra were measured using a photoluminescence spectrometer (f = 0.5 m, Acton Research Co., Spectrograph 500i, USA) and an intensified CCD (PI-MAX3) (Princeton Instrument Co., IRY1024, USA). A DPSS (diode pumped solid state) laser (Ekspla), with a wavelength of 266 nm and a power of 310 mW, was utilized as an excitation source for PL measurement.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-nanoflowers,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Hydrothermal,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"ITO glass (Kintec, 15 \\u03a9 sq\\u22121) was cleaned sequentially with deionized water, acetone, and isopropanol in an ultrasonic bath for 10 min. ZnO precursor solution consisting of 0.100 g zinc acetate dihydrate and 28.0 \\u03bcl monoethanolamine in 1 ml of 2-methoxyethanol was stirred at room temperature overnight. The resulting solution was filtered using a 0.45 \\u03bcm PTFE membrane filter prior to spin coating at 2000 rpm. The obtained ZnO films were annealed at 200 \\u00b0C for 1 hour in air. Precursor cesium bromide (CsBr, 99.9% from Aldrich) and lead(II) iodide (PbI2, 99.9% from Aldrich) were thermally co-evaporated in a vacuum chamber integrated inside an MBraun glove box (4 \\u00d7 10\\u22126 mbar) at the balanced deposition rates of 0.5\\u20132 \\u00c5 s\\u22121, producing CsxPbI2Brx films with x ranging from 0.95 to 4 and total thickness of 150 \\u00b1 10 nm. The thermal evaporation sources were carefully calibrated to achieve high accuracy and reproducibility in the thickness of the deposited films. Sequential layer-by-layer deposition of CsBr and PbI2 with the balanced layer thicknesses provided the required composition of the perovskite films. Composition of the films was additionally verified using flame atomic absorption spectrometry (see Table S1, ESI\\u2020). The freshly grown CsxPbI2Brx films were annealed at 270 \\u00b0C for 10 min in a nitrogen atmosphere inside the glove box. A P3HT hole transport layer was deposited by spin-coating (15 mg ml\\u22121 in chlorobenzene) at 1200 rpm for 50 s. Top Au electrodes (150 nm) were thermally evaporated through a shadow mask in vacuum (5 \\u00d7 10\\u22126 mbar). The device active area was in the range of 0.3\\u20130.4 cm2. The devices were characterized by I\\u2212V and EQE measurements as reported previously.\\n\\nCs/Pb atomic ratio in the deposited CsxPbI2Brx films was verified using flame atomic absorption spectrometry. The perovskite films were washed off from the glass substrates with 1 ml of 0.5 M KOH solution to obtain aqueous solutions. Next, the obtained solutions were quantitatively transferred with deionized water into volumetric flasks for quantitative measurements. The analysis was performed using a Zeiss AAS-3 spectrophotometer. Hollow cathode lamps for Pb and Cs were used as light sources, which operated at the current of 7 mA and wavelengths of 283.3 and 852.1 nm, respectively. Air/acetylene stoichiometric mixture was used to generate the flame. The relative standard deviations of the measurements were within 1%.\\n\\nScanning electron microscopy (SEM) images were obtained on a Zeiss SUPRA 25 instrument. The samples were prefixed on a microscope stage inside a glove box to reduce the exposure time in air down to \\u223c3\\u20135 min.\\nThe scanning probe microscopy measurements were conducted on a Cypher ES microscope (Asylum Research, CA) under dry inert Ar atmosphere in an MBraun glovebox with O2 < 0.1 ppm and H2O < 1 ppm. Electrical contact to the sample was provided through ITO and conductive Ag paint. Photocurrent was measured in a conductive SPM mode (c-SPM) with 1 V bias applied to the sample. Additional current\\u2013voltage measurements were performed with the triangular voltage ramp from \\u22122 V to +2 V. A fully platinum cantilever from Rocky Mountain (25PT300B) was used. As the light source we used a Cypher Blue Drive laser diode with 405 nm wavelength. Power density was set to 122 mW cm\\u22122.\\n\\nA pulsed laser beam (Coherent Legend-Elite, 800 nm, 1 kHz repetition rate, pulse duration \\u223c35 fs) was split into three beams. One beam was used to generate a 400 nm beam through a beta-barium borate (BBO) crystal via second harmonic generation, the second one was used to generate a THz beam though a 1 mm-thick ZnTe crystal via optical rectification, and the third one was used to detect the transmitted terahertz electric field via electro-optic sampling in another ZnTe crystal. The samples were excited with 400 nm laser pulses (16.6 \\u03bcJ cm\\u22122) and probed with THz pulses at a well-defined pump\\u2013probe delay \\u03c4. The samples were deposited on z-cut quartz substrates, and bare z-cut quartz substrates were used to obtain the reference signal. Firstly, we measured transmitted THz electric field E(t,\\u03c4) and photoinduced change in THz electric field \\u0394E(t,\\u03c4) simultaneously, denoting Esam(t,\\u03c4) and \\u0394Esam(t,\\u03c4) for the sample on quartz and Eref(t,\\u03c4) and \\u0394Eref(t,\\u03c4) for the reference. Secondly, we calculate the transmittance at every pump\\u2013probe delay \\u03c4 from the transmitted THz electric field through the sample. Thirdly, we extract complex refractive indexes (\\u00f1 = n + ik) at \\u03c4 from the transmittance:\\nwhere, \\u00f1sub is the refractive index of the z-cut quartz substrate, d is the film thickness, c is the speed of light in a vacuum, and \\u0394L is the thickness difference between the sample and reference substrates.\\nWe then calculate the complex conductivity at \\u03c4, and the equilibrium conductivity 0 (\\u03c4 < 0) through the equations , and = 1 + i/\\u03c9\\u03b50. Finally we obtain the photoconductivity \\u0394 = \\u0394\\u03c31 + i\\u0394\\u03c32via \\u0394(\\u03c4) = (\\u03c4) \\u2212 0.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBrI2,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Evaporation,\\n Perovskite_deposition_thermal_annealing_temperature: 270,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 70.0; 70.0,\\n Stability_atmosphere: N2,\\n Stability_time_total_exposure: 500,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.3,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals and reagents were used as received from chemical companies, including PbI2 (>98%, TCI), PbBr2 (99%, Sigma-Aldrich), HI (48% in water, Sigma-Aldrich), HBr (48% in water, Sigma-Aldrich), CH3NH2 (33 wt% in absolute ethanol, Sigma-Aldrich), formamidine acetate (99%, Sigma-Aldrich), titanium diisopropoxide bis(acetylacetonate) 75% in isopropanol (Tiacac, Sigma-Aldrich), mesoporous-TiO2 paste (18NR-T, Dyesol), Li-bis(trifluoromethanesulfonyl) imide (LiTFSI, Sigma-Aldrich), 4-tert-butylpyridine (TBP, 96%, Sigma-Aldrich), 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4TCNQ, 97%, Sigma-Aldrich), poly(3-hexylthiophene-2,5-diyl) (P3HT, regioregular, Sigma-Aldrich).\\nThe NHCHNH3I was synthesized according to a previously literature. 28.1 ml of HI was slowly dropped into 10 g formamidine acetate in methanol solution cooled at 0 \\u00b0C with vigorous stirring for 5 hours. The resulting solution was concentrated by rotary evaporation at 80 \\u00b0C until all the precipitate dissolve out, then the crude solid was dissolved by methanol and re-precipitated in diethyl ether. After recrystallization for 3 times, the white powder was dried at 80 \\u00b0C under vacuum for 2 days to afford the desired pure NHCHNH3I.\\nThe CH3NH3Br (MABr) was synthesized by slowly dropping 31.1 ml of HBr into 33.8 ml CH3NH2 ethanol solution cooled at 0 \\u00b0C with vigorous stirring for 5 hours. The resulting solution was concentrated by rotary evaporation at 50 \\u00b0C until all the precipitate dissolve out, then the crude solid was dissolved by ethanol and re-precipitated in diethyl ether. After recrystallization for 3 times, the white powder was dried at room temperature under vacuum for 2 days to afford the desired pure MABr.\\nThe mixed-cation perovskite precursor solution of (FAPbI3)1\\u2212x(MAPbBr3)x (x = 0.15) was prepared in a glovebox, by dissolving the FAI (1 M), MABr (0.2 M), PbI2 (1.1 M) and PbBr2 (0.2 M) in a mixed solvent of dimethyl formamide (DMF) and dimethyl sulfoxide (DMSO) (4:1, v/v), as reported previously.\\n\\nFluorine-doped tin oxide (FTO)-coated glass (Pilkington TEC 15) was firstly patterned by etching with Zn powder and 2 M HCl. The etched substrate was then sequentially cleaned by using detergent, de-ionized water and ethanol. Remaining organic residues were removed under oxygen plasma for 30 min. A compact TiO2 blocking layer (BL) of roughly 30\\u201340 nm was deposited on the cleaned FTO glasses by spray pyrolysis of titanium diisopropoxide bis(acetylacetonate) diluted in anhydrous ethanol at a volumetric ratio of 1:10 and then heated at 500 \\u00b0C for 30 min. A mesoporous TiO2 layer was deposited by spin-coating TiO2 paste (Dyesol 18NR-T) diluted in anhydrous ethanol at ratio of 1:5 by weight at 5000 rpm for 30 s. The layers were then sintered in air at 500 \\u00b0C for 30 min. The mixed-cation perovskite films were deposited onto the mesoporous TiO2/BL TiO2/FTO substrates from the precursor solution by a two-step spin-coating procedure, at 1000 rpm for 30 s and then 5000 rpm for 20 s. During the second step, 200 \\u03bcl of chlorobenzene was dropped onto the substrates 10 s prior to the end of the program. The substrate was directly heated on a hotplate at 100 \\u00b0C for 60 min. After cooling to room temperature, different doping level of P3HT:F4TCNQ composites were deposited on the perovskite layers at 2000 rpm for 30 min via solution process. 20 mg ml\\u22121 P3HT solution was prepared by dissolving 20 mg P3HT in 1 ml ortho-dichlorobenzene (DCB), stirred at 70 \\u00b0C for 30 min. p-Type doping material F4TCNQ in DCB solution with a concentration of 2 mg ml\\u22121 was also stirred at 70 \\u00b0C for 30 min before adding to the P3HT solution. In addition, for comparison, 9.1 \\u03bcl of a stock solution of 28.5 mg ml\\u22121 LiTFSI in acetonitrile (ACN) and 4.5 \\u03bcl 4-tert-butylpyridine (TBP) was mixed into 1 ml P3HT (20 mg) solution as HTM solution. After spin coating of the HTM layers, the substrates were heated at 65 \\u00b0C for 15 min. Finally, a layer of 100 nm Au was deposited on top of the HTM layer under high vacuum (<4 \\u00d7 10\\u22124 Pa) by thermal evaporation.\\nThe photocurrent\\u2013voltage (J\\u2013V) characteristics of the solar cells were measured using a Keithley 2400 Source-measure unit under illumination of a simulated sunlight (AM 1.5G, 100 mW cm\\u22122) provided by an Oriel Sol3A solar simulator (Newport USA, Model: 94023A) with an AM 1.5 filter in ambient air. Light intensity was calibrated with a Newport calibrated standard Si reference cell (SER. no. 506/0358). A black mask with a circular aperture (0.09 cm2) smaller than the active area of the square solar cell (0.20 cm2) was applied on top of the cell. The J\\u2013V curves were obtained from forward bias to short-circuit at a scan rate of 20 mV s\\u22121. The incident photo-to-current conversion efficiency (IPCE) was measured by Oriel IQE 200 (Newport USA, Model: 94023A/PVIV-212V/IQE-AC-QTH-SI-220). Prior to measurement, a standard silicon solar cell was used as reference.\\n\\nThe top view and cross-section scanning electron microscopy (SEM) images were obtained by HR-SEM performed with FEI (Field Emission Instruments: Nova Nano SEM 450), the USA. Conductivity measurements were performed as follows. Glass substrates were sequentially cleaned by detergent, de-ionised water and ethanol. Remaining organic residues were removed under oxygen plasma for 30 min. A thin layer of compact TiO2 (\\u223c30 nm) was coated on the glass substrates. After sintering the TiO2 film at 500 \\u00b0C for 30 min, the film was cooled to room temperature. A solution of HTM in DCB was spin-coated onto the TiO2 substrate, whereas the concentration was the same as in case for the photovoltaic device. Finally, a 200 nm-thick of Ag was deposited on the top of the HTM by thermal evaporation under high vacuum (<4 \\u00d7 10\\u22124 Pa). A two-point probe setup was used with a Keithley 2400 source meter for measuring linear current\\u2013voltage curves. The electrochemical impedance spectroscopy (EIS) measurements were carried out at different applied bias in the dark condition using an impedance/gain-phase analyser (Zahner Model: Zennium, Serial No. 40037, German) electrochemical workstation with the scanning frequency range from 106 to 0.1 Hz. The magnitude of the alternative signal was 10 mV. The UV-Vis spectra were measured by Agilent 8453 spectrophotometer (Model: HP 8435, China). The infrared spectra were measured by Fourier transform infrared spectrometer (FTIR) mode on 6700 (ThermoFisher, USA).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.83MA0.17PbBr0.51I2.49,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.2,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Guanidinium iodide (GAI, 99%), butylamine hydroiodide (BAI, 99%) and bathocuproine (BCP, 99%) were purchased from TCI. Formamide (99.5%), chloroform (CF, 99%) and ethyl alcohol (99%) were ordered from Sigma Aldrich. Methylammonium iodide (MAI, 99%) was purchased from Shanghai Mater Win New Materials. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) aqueous solution (Al 4083) was purchased from Baytron. Poly[sodium 3,3\\u2032-(2-([1,1\\u2032-biphenyl]-4-yl)-4H-cyclopenta[2,1-b:3,4-b\\u2032]dithiophene-4,4-diyl)bis(propane-1-sulfonate)] (PCP-Na) was purchased from Solarmer Materials inc. (6,6)-Phenyl-C61-butyric acid methyl ester (PCBM, 99%) was purchased from American Dye Source. PbI2 (99%) and N,N-dimethylformamide (DMF, 99%) were purchased from Alfa Aesar. All reagents and solvents were used directly if not specified.\\n\\nThe ITO coated glass substrates were cleaned sequentially in detergent (Hellmanex, 2 vol%), deionized water, acetone, and an isopropanol ultrasonic bath for 15 min, respectively. After that, the substrates were dried in nitrogen flow and cleaned by UV-Ozone treatment for 20 min before use. The PEDOT:PSS HTL was prepared by spin coating PEDOT:PSS aqueous solution at 4000 rpm for 40 s, followed by annealing at 140 \\u00b0C for 20 min. The PCP-Na HTL was prepared by spin coating a 0.5 mg ml\\u22121 PCP-Na methanol/H2O mixed solution (7:3) at 4000 rpm for 40 s, followed by annealing at 140 \\u00b0C for 20 min. GAI, BAI, MAI and PbI2 were mixed in a 0.2:1.8:4:5 molar ratio (n = 5) in DMF (with or without 3% formamide addition) with the concentration of 0.4 M (based on Pb). The perovskite precursor solution and PEDOT:PSS/PCP-Na substrates were heated to 70 \\u00b0C before spin coating the perovskite layer. The spin-coating process started initially at 1000 rpm for 10 s and then 6000 rpm for 60 s after dropping the heated precursor to the heated PEDOT:PSS/PCP-Na substrates, followed by annealing at 100 \\u00b0C for 10 min. PCBM (5 mg ml\\u22121 in CF) was spin-coated on the perovskite at 2000 rpm for 30 s. BCP (0.5 mg ml\\u22121 in ethyl alcohol) was then spin-coated on PCBM at 3000 rpm for 30 s, followed by deposition of 100 nm Ag in a vacuum chamber under a high vacuum of 5 \\u00d7 10\\u22124 Pa.\\nUltraviolet photoelectron spectrometer (UPS) measurements were conducted on an ESCALAB 250Xi (Thermo) system, and the energy of the incident light energy for UPS measurement was 21.22 eV. The field-emission scanning electron microscope (FESEM) measurements were carried out on a Hitachi S-4800 machine. Crystallographic properties of the perovskite films were investigated using a Rigaku Ultima IV diffractometer with Cu K\\u03b1 radiation of 0.15406 nm (graphite mono-chromatic) at a scanning rate of 10\\u00b0 min\\u22121. GIWAXS measurements were carried out with a Xeuss 2.0 SAXS/WAXS laboratory beamline using a Cu X-ray source (8.05 keV, 1.54 \\u00c5) and a Pilatus3R 300K detector. The incidence angle was 0.3\\u00b0. The UV-Visible absorption spectra were taken on a UV-2450 UV-Vis Shimadzu Spectrophotometer. The steady-state PL spectra were taken on an FLSP920 from Edinburgh Instruments, using a xenon lamp at an excitation wavelength of 470 nm.\\nThe photocurrent density\\u2013voltage (J\\u2013V) measurement was performed via a solar simulator (SS-F5-3A, Enlitech) along with AM1.5G spectra whose intensity was calibrated using the certified standard silicon solar cell (SRC-2020, Enlitech) at 100 mV cm\\u22122. The external quantum efficiency (EQE) data were obtained by using the solar-cell spectral-response measurement system (QE-R, Enlitech). The perovskite solar cells were kept in a humidity-controlled cabinet (Hr = 50 \\u00b1 5% and 25 \\u00b1 5%, Bossmen, PR1852(A)-SH) for humidity-stability measurement. We performed a heat stability measurement by placing devices on an 85 \\u00b0C hotplate in a glovebox, and conducted a light stability measurement via illuminating the devices under AM1.5G illumination (100 mW cm\\u22122) in an air environment without encapsulation, and the temperature was 40 \\u00b0C.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: BAGUMA4Pb5I16,\\n Perovskite_composition_short_form: BAGUMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PCP-Na,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 700,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 91,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals and materials were purchased and used as received unless otherwise noted. CH3NH3I, CH3NH3Br, and HC(NH2)2I (FAI) were purchased from Dyesol and used as received. PbI2 (99.99%) and PbBr2 (99.99%) were purchased from TCI. PbCl2 (99.999%) and CsI (99.9%) were purchased from Sigma Aldrich. NiOx NC inks were prepared according to our previous reports.\\n\\nITO-coated glass substrates were cleaned and then ultraviolet-ozone treated for 20 min. The NiOx NC ink (20 mg mL\\u22121 in DI-water) was spin-coated to obtain a 20 nm NiOx film. The resultant NiOx films will be used to fabricate devices without an annealing process or other treatments. The perovskite solutions were prepared by reacting CH3NH3I (190 mg) with PbI2 (500 mg) and PbCl2 (30 mg) in anhydrous N,N-dimethylformamide (1 mL) at room temperature. To deposit the perovskite film, the precursor solution was first dropped onto a NiOx/ITO substrate. The substrate was then spun at 5000 rpm and after six seconds anhydrous chlorobenzene (180 \\u03bcL) was quickly dropped onto the center of the substrate, and dried on a hot plate at 100 \\u00b0C for 10 min. Subsequently, the fullerene mixture (8 mg PCBM + 12 mg C60 in 1 mL dichlorobenzene) and zirconium(IV) acetylacetonate (Zracac) (2 mg mL\\u22121 in anhydrous ethanol) were then sequentially deposited by spin coating at 1000 rpm for 60 s and 4000 rpm for 40 s, respectively. Finally, the device was completed with the evaporation of Ag contact electrodes (120 nm) in a high vacuum through a shadow mask. The Cs5(MA0.17FA0.83)95Pb(I0.83Br0.17)3 mixed perovskite was prepared according to the previous report. For MPP tracking, a copper electrode was deposited. All devices were fabricated in a glove box.\\n\\nThe as-prepared PVSCs were covered by a glass petri dish. Around 10 \\u03bcL diethylenetriamine (DETA) was added at the edge of the petri dish. Since the boiling point of DETA is 204 \\u00b0C, DETA vaporized in the petri dish and modified the perovskite devices moderately at room temperature. The duration of PDL treatment is in the range from 10 min to 30 min.\\n\\nThe XRD spectrum was obtained using a D5005 X-ray diffraction system (CuK\\u03b1 radiation, \\u03bb = 1.54056 \\u00c5). UV-vis absorption spectra were obtained from a home-build system with a xenon lamp as a light source and an integrated sphere associated with a charge-coupled device (Ocean Optics QE Pro) as a detector. SEM images were recorded using a LEO 1530 scanning electron microscope. X-ray photoelectron spectroscopy (XPS) of perovskite films was measured in the ultrahigh vacuum environment using Physical Electronics PHI 5802 with a monochromatic Al K\\u03b1 X-ray source. Ultraviolet photoelectron spectroscopy (UPS) was characterized by using a He discharged lamp (He I 21.22 eV, Kratos Analytical). The J\\u2013V curves were recorded from 0 to 1.2 V using a Keithley 2635 apparatus with the scan rate being 0.10 V s\\u22121. Solar-simulated AM 1.5 sunlight was generated using Newport AM 1.5G irradiation (100 mW cm\\u22122), calibrated with an ISO 17025-certified KG3-filtered silicon reference cell. The spectral mismatch factor was calculated to be less than 1%. To avoid the side edge effect, a black mask with an aperture area of 3.36 mm2 was employed during the J\\u2013V measurement. The scan speeds for all J\\u2013V curves are 0.10 mV s\\u22121. The IPCE measurement was performed by a system combining a xenon lamp, a monochromator (SpectraPro-2150i, Acton Research Corporation), a chopper, two optical filters (320 and 570 nm), and a lock-in amplifier (SR830, Stanford Research Systems) together with a calibrated silicon photodetector (Hamamatsu mono-Si cell). The impedance measurement was carried out by a Zahner electrochemistry station (Zennium Pro) with a DC bias of 0.1 V and a frequency range from 1 Hz and 1 MHz with an AC amplitude of 10 mV under illumination with a white LED array (100 mW cm\\u22122 intensities). The steady-state and time-resolved photoluminescence of perovskite on glass were investigated using PicoQaunt FluoTime 300. A picosecond 375 nm pulse laser (LDH-P-C-375) with a pulse width of <40 ps and a repetition rate of 2 MHz was used to excite the perovskite. The time-resolved single photon counting was performed by a time-corrected single photon counting (TCSPC, PicoHarp 300E) module with a photomultiplier (PMA-C 192-M) detector. The obtained data were fitted using a bi-exponential function below:\\n\\nAll calculations are performed based on the density functional theory as implemented in the VASP code. For the exchange\\u2013correlation functional, we use the generalized gradient approximation (GGA) within the Perdew Burke Ernzerhof (PBE) functional. The plane wave cut-off energy is 500 eV. For the (001) surface of \\u03b2-MAPbI3, the k-point mesh is 4 \\u00d7 4 \\u00d7 1 based on the \\u0393 point. With the introduction of a vacancy of Pb and the IDEA passivation, the surface is enlarged to 2 \\u00d7 2 \\u00d7 1 of the perfect (001) surface and the k-point mesh is 2 \\u00d7 2 \\u00d7 1 based on the \\u0393 point.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60; PCBM-60 | Zr(acac)4,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-np,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 200,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 50,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"For the wearable devices, pre-stretched PDMS (sylgard 184, 110 \\u03bcm) was selected as the substrate, and it was attached on a pre-cleaned glass for the following process. To fabricate transparent electrodes for wearable PSCs, a highly conductive PEDOT:PSS (Heraeus CLEVIOSTM PH1000) aqueous solution with 5 wt% glycol and 0.5 wt% Zonyl FS-300 (Dupont) was spun onto the PDMS substrates at 1000 rpm for 30 s, followed by 1500 rpm for 10 s, and subsequently annealed at 100 \\u00b0C for 15 min. The conductivity was over 4000 S cm\\u22121, which is comparable to that of PET/ITO. The sheet resistance of final PEDOT:PSS electrode was about 40 \\u03a9 \\u25a1\\u22121. To match the energy level of device, a hole-transport layer (HTL) PEDOT:PSS (Heraeus CLEVIOSTM Al4083) was then spin-coated onto PH1000 anode at 5000 rpm for 1 min, which was heated at 100 \\u00b0C for 15 min. As for cathode, the PEI (Aldrich, 0.1 wt% diluted by isopropanol) layer was spin-coated on top at 5000 rpm for 30 s and then dried in air for 10 min. The 3 M copper tape was used to adhere to the electrode using silver glue.\\n\\nThe PVK films were prepared via a single-step process from a solution containing 549 mg PbI2 (Sigma-Aldrich), 46 mg PbBr2 (Sigma-Aldrich), 150 mg HC(NH2)2I (Xi\\u2019an p-OLED Corp.), 40 mg CH3NH3I (Xi\\u2019an p-OLED Corp.) and an appropriate concentration of PU (Sigma-Aldrich) in 800 \\u03bcl anhydrous DMF (Sigma-Aldrich) and 200 \\u03bcl anhydrous DMSO (Sigma-Aldrich) mixture solvent. The spin-coating was started at a rotation speed of 4000 rpm for 30 seconds. A trace of SBS (Aladdin) anhydrous chlorobenzene (Sigma-Aldrich) solution was drop-casted quickly within 7 seconds after reaching high speed. Then, the perovskite films were heated at 100 \\u00b0C on a hotplate for 30 min. After that, \\u223c60 nm-thick [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM, ADS) was spin-coated from a anhydrous chlorobenzene solution (20 mg ml\\u22121) at 2000 rpm for 40 s. After drying, the top PEI/PEDOT:PSS/PDMS electrode was deposited via a film-transfer lamination technique: the bottom device was first exposed to air-plasma for about 2 s (flash). Then, PEI/PEDOT:PSS/PDMS electrode was transferred onto the PC61BM film and encapsulated using a vacuum-laminator. The top PDMS layer provided passivation for device encapsulation. It showed excellent long-term stability with different humidities and thermal conditions (Fig. S24, for more details, please see the ESI\\u2020).\\n\\nThree single chips (9.33 cm2) were fabricated in a parallel circuit to create a unit. Two units were fabricated in series to complete the wearable solar cell module (certified 56.02 cm2). All circuits were fabricated using a gold-wire bonding machine. The wearable experiments were tested under LED light irradiation (\\u223c20 klx solar irradiance).\\n\\nCurrent\\u2013voltage (J\\u2013V) characteristics of the solar cells were characterized using a Keithley 2400 instrument. The currents were measured under a solar simulator (Enli Tech, 100 mW cm\\u22122, AM 1.5 G irradiation). The reference silicon solar cell was corrected from NREL. All the measurements were performed in an ambient atmosphere at room temperature. The scan range is from 0 V to 1.2 V or from 1.2 V to 0 V and 8.0 mV for each step. The delay time is 30 ms, and the scan rate is 267 mV s\\u22121. All the J\\u2013V curves were based on 150 points. All the active areas were corrected by calibrated masks (1.01, 2.24, 3.99, 6.23 and 9.33 cm2). The repeated bending and stretching cycles were performed using a custom-made stretching machine, which was actuated by a stepper motor. All the results of bending tests were averaged from over 20 samples. The incident photo-to-electron conversion efficiency spectra (IPCE) were detected under monochromatic illumination (Oriel Cornerstone 260 1/4 m monochromator equipped with Oriel 70613NS QTH lamp), and calibration of the incident light was performed using a monocrystalline silicon diode.\\n\\nThe morphology of films was measured by SEM (JEOL, JSM-7500F, Japan) at an accelerating voltage of 5.0 kV and AFM (nanoscope multimode Bruker). The CSAFM images and limit deflection curves were investigated using specific probes. XRD and 2D-XRD images were recorded using a D8-Discover 25 diffractometer (Bruker). Absorbance spectra measurement was analyzed by UV-vis spectroscopy (SHIMADZU, UV-2600). FTIR spectra were recorded using an infrared spectrometer (Bruker TENSOR-27). XPS studies were performed using a Thermo-VG Scientific ESCALAB 250 photoelectron spectrometer equipped with a monochromated Al K\\u03b1 (1486.6 eV) X-ray source. All recorded peaks were corrected for electrostatic effects by setting the C\\u2212C component of the C 1s peak to 284.8 eV. The base pressure in the XPS analysis chamber was 2 \\u00d7 10\\u22129 mbar. Steady-state photoluminescence and TRPL measurements at the peak emission of \\u223c770 nm (on the excitation at 470 nm) were carried out using a steady state and lifetime spectrometer (FLS920, Edinburgh Instruments Ltd). All the PL samples were fabricated on PDMS/PEDOT:PSS electrodes. The thickness of all the samples was detected using a surface profiler (Bruker).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: PDMS,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.83MA0.17PbBr0.51I2.49,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: PEI | PEDOT:PSS | PDMS,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Lamination,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 60,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 1.01,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Laser-ablated FTO glass (Pilkington TEC-7, 7 \\u03a9 sq\\u22121) was successively rinsed with detergent, deionized water, acetone and ethanol by an ultrasonic bath for 20 min, respectively. Subsequently, the substrates were treated with oxygen plasma for 15 min. A thin compact TiO2 (c-TiO2) layer was deposited on substrates by spin-coating 0.15 M titanium diisopropoxide in 1-butanol at 2500 rpm for 40 s, and then sintered at 500 \\u00b0C for 1 h in an oven. The 0.73 M MAPbI3 perovskite precursor solution was prepared by mixing PbI2, MAI and MACl (1:1:1, molar ratio) in N,N-dimethylformamide (DMF). The MAxFA1\\u2212xPbI3 perovskite precursor solution was prepared by mixing PbI2, MAI, FAI and MACl (1:0.4:0.6:1.2, molar ratio, x = 0.4) in DMF. The 0.73 M FAPbI3 perovskite precursor solution was prepared by mixing PbI2, FAI and MACl (1:1:1, molar ratio) in DMF. The perovskite solutions were spin-coated on the substrates at 2500 rpm for 40 s, then annealed at 100 \\u00b0C for 60 min for MAPbI3 and MA0.4FA0.6PbI3 perovskite films, while at 120 \\u00b0C for 60 min for the FAPbI3 perovskite film. After the deposition of the perovskite layer, the hole transport layer (HTL) was coated at 4000 rpm for 30 s. The HTL solution was prepared by dissolving 72.3 mg of 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene in 1 mL of chlorobenzene, to which 28.8 \\u03bcL of 4-tert-butylpyridine, 17.5 \\u03bcL of 520 mg mL\\u22121 lithium bis(trifluoromethylsulphonyl)imide in acetonitrile and 28.8 \\u03bcL of 300 mg mL\\u22121 tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)-cobalt(III) bis(trifluoromethylsulphonyl)imide in acetonitrile were added. Finally, an 80 nm-thick Au counter electrode was deposited by thermal evaporation. Unless otherwise stated, all materials were purchased from Alfa Aesar and used as received.\\n\\nThe morphologies of the perovskite films were characterized by field-emission scanning electron microscopy (FE-SEM, Hitachi SU8010) at an accelerating voltage of 5 kV and were determined at 200 kV using high-resolution transmission electron microscopy (HRTEM, JEOL JEM-2010). The perovskite samples were dispersed in chloroform and dropped onto the surface of a copper grid. X-ray diffraction (XRD) analysis was conducted on a Shimadzu XRD-7000 diffractometer using Cu K\\u03b1 radiation in the 2\\u03b8 range from 10\\u00b0 to 60\\u00b0 at a scan rate of 2\\u00b0 per min. UV-vis absorption spectra were recorded on a Shimadzu UV-3600 spectrometer. Steady-state photoluminescence (PL) spectroscopy was carried out by using an Edinburgh FLS980 spectrometer at an excitation wavelength of 510 nm with irradiation from the side of spin-coated materials. TRPL was performed using a picosecond diode laser (EPL-470, 95 ps) and the signal was recorded at 775 nm (MAPbI3), 795 nm (MA0.4FA0.6PbI3) and 810 nm (FAPbI3) after excitation at 475 nm. The measurement conditions were the same as the steady-state PL.\\nThe current density (J)\\u2013voltage (V) characteristics were obtained by exposing the targeted cells to a standardized sunlight simulator, which was calibrated by a standard silicon reference cell to AM 1.5G one-sun illumination (100 mW cm\\u22122), with sweeping over of the predetermined applied bias voltage range from open circuit to short circuit (reverse scan) at a scan rate of 1 mV s\\u22121 without light soaking or voltage treatment history. A metal aperture mask was used to fix the active area to 0.1 cm2, and all data were acquired by a Keithley 2400 SourceMeter.\\n\\nTPV measurements were conducted following a previous report. The targeted cell was kept under open-circuit conditions and was irradiated by a continuous-wave LED laser (520 nm, RGB photonics, Lambda beam) to maintain a steady-state photovoltage (Vph). Then weak laser pulses (532 nm, 7 ns) were applied to induce a small increase (\\u0394Vph) in Vph, with \\u0394Vph/Vph \\u2264 5%. Finally, electric signals were recorded on a digital oscilloscope (64Xs, Lecroy; Input impendence, 1 M\\u03a9). A series of desired Vph was obtained by adjusting the intensity of the LED laser through laser power and neutral filters.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylamine solution (40 wt% in ethanol), hydriodic acid (57 wt% in H2O) and lead (II) iodide (PbI2, 99.999%) were purchased from Alfa or Sigma-Aldrich. Phenyl-C61-butyric acid methyl ester (PCBM) was obtained from Solamer Materials Inc. Methylammonium iodide (MAI) was synthesized according to the literature by stoichiometrically reacting methylamine with hydriodic acid . The perovskite precursor was prepared by mixing MAI and PbI2 in a molar ratio of 1:1 in anhydrous N,N-dimethylformamide (DMF, 99.8%, Alfa), and the final concentration of the perovskite was controlled to approximately 40 wt%. The solution was stirred overnight at room temperature and filtered with 0.45 \\u03bcm PVDF filters before spin-coating. The molecular structure of PDINO is shown in Fig. 1 c, and its synthesis and characterization was reported elsewhere .\\n\\nFirst, the patterned ITO substrates were sequentially ultrasonic cleaned with detergent, deionized water, acetone and isopropanol. On cleaned ITO substrate, PEDOT:PSS aqueous solution filtered through a 0.45 \\u03bcm PVDF filters was spin-coated at 4,000 rpm for 30 s and then annealed at 150 \\u00b0C in air for 15 min. The CuSCN was potentiostatically electrodeposited for 50 s from an aqueous solution of 12 mmol L\\u22121 copper sulfate (CuSO4), 12 mmol L\\u22121 ethylenediaminetetraacetic acid (EDTA) and 12 mmol L\\u22121 potassium thiocyanate (KSCN) at a fixed potential of \\u22120.3 V versus Ag/AgCl (3 mol L\\u22121 KCl) . After drying with nitrogen, The as-prepared perovskite precursor solution was spin coated onto the ITO/PEDOT:PSS or ITO/CuSCN substrate at a speed of 5000 r.p.m for 30 s. During the last 4.5 s of the spinning process, chlorobenzene was quickly added to induce the fast crystallization. Then the substrate was dried on a hot plate at 100 \\u00b0C for 10 min. The PCBM (20 mg mL\\u22121 in chlorobenzene) and PDINO (1 mg mL\\u22121 in methanol) were then sequentially deposited by spin coating at 1,500 rpm for 30 s and 3,000 rpm for 30s, respectively. Finally, a 100 nm Al electrode was deposited on PDINO layer under a high vacuum through a shadow mask by thermal evaporation with an active area of 0.05 cm2.\\n\\nThe current density\\u2212voltage (J\\u2013V) characteristics were measured by a computer\\u2212controlled Keithley 2450 Source\\u2212Measure Unit. The light source was Oriel Sol3A Class AAA Solar Simulator (model, Newport 94,023A) with a 450 W xenon lamp and an air mass (AM) 1.5 filter. The light intensity was calibrated to 100 mW cm\\u22122 by a reference cell (Newport Oriel 91150 V). The EQE spectra were recorded with an Enli Technology (Taiwan) EQE measurement system (QE-R), and the light intensity at each wavelength was calibrated with a standard single-crystal Si photovoltaic cell. The thickness of the film was measured by a Profilometer (Ambios Tech. XP\\u20132). The scanning electron microscopy (SEM) was performed in order to investigate the morphology of the perovskite films prepared on top of PEDOT:PSS or CuSCN. Top-view and cross-section images was characterized by HITACHI s-4800 (Hitachi Limited, Japan) using an InLens detector operating at an accelerating voltage of 10 kV. The atomic force microscopy (AFM) images were obtained by utilizing SPA-400 SPM (Seiko Instrument, Inc.). The X-ray diffraction (XRD) patterns were recorded on a D/MAX-2000 X-ray diffractometer with monochromated Cu K\\u03b1 irradiation (\\u03bb = 1.5418 \\u00c5). The electrodeposition of the CuSCN layer and the EIS measurements were performed on a Zennium electrochemical workstation (Zahner Instrument, Inc.).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PDINO,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 23.5; 23.5,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 190,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 30,\\n Cell_area_measured: 0.05,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials were purchased from Aldrich, unless otherwise specified, and they were used as received. Commercial nanocrystalline titania Degussa P25 was used in all cell constructions and Millipore water was used in all experiments. SnO2:F transparent conductive electrodes (FTO, Resistance 8 \\u03a9/square) were purchased from Pilkington.\\n\\nA mixture of 4-butylphthalonitrile (1.0 g, 5.4 mmol), copper(II) chloride (0.24 g, 1.8 mmol), 1,8-diazabicyclo[5.4.0]undec-7-ene (0.2 mL), and 1-pentanol (2 mL) were stirred at reflux under argon for 2 h. The reaction mixture was cooled to room temperature and petroleum ether (50 mL) was added to precipitate the product. The suspension was stirred for 5 min, filtered and the residue washed with CH2Cl2 (30 mL). The filtrates were combined and the solvent was removed by rotary evaporation. The crude product was purified by column chromatography with CH2Cl2/ethanol (v/v, 1/3) as the eluent to give a blue product. The product was further purified by repeated recrystallization from CH2Cl2/ethanol to give CuBuPc (0.38 g, 35%). To fulfill the requirements of electronic applications, the product was further purified by vacuum sublimation in a sublimation machine (Technol VDS-80) operated at 400 \\u00b0C and \\u223c3 \\u00d7 10\\u22123 Pa. Elemental analysis calcd (%) for C48H48CuN8: C, 72.02; H, 6.04; N, 14.00; found: C, 71.89; H, 6.10; N, 13.89. ESI-MS: m/z (M + ) 799.33. UV\\u2013vis (CHCl3): \\u03bbmax = 678 nm (195625 L mol\\u22121 cm\\u22121), 611 nm (43360 L mol\\u22121 cm\\u22121). IR (KBr): \\u03bd = 2950, 2924, 2855, 1611, 1504, 1456, 1405, 1337, 1159, 1095, 1064, 819, 737, 720 cm\\u22121.\\n\\nGO was synthesized from pre-oxidized graphite flakes by the Hummers and Offeman method . Briefly, in the first step, 5 g of graphite flakes (99.95%), 3 g of K2S2O8 and 3 g of P2O5 were dissolved in 20 mL concentrated H2SO4 (95 wt.%) and stirred at 80 \\u00b0C for about 8 h. The resultant mixture was then diluted with 1 L deionized water and filtered using a porous membrane (0.45 micron). Washing procedure was carried out until achieving neutral pH. The pre-oxidized graphite flakes were obtained by drying the final product at 40 \\u00b0C overnight. In a second step, the above oxidized graphite powder was added into 100 mL concentrated H2SO4 (95 wt.%) in an ice bath (0 \\u00b0C) and were stirred until dissolution. 12 g of KMnO4 and 4 g of NaNO3 were then added gradually and successively into the mixture, controlling its temperature around 20 \\u00b0C. The cooling bath was then removed and the solution was transferred to a 35 \\u00b0C water bath for gas releasing under continuous stirring for about 1 h to obtain a thick green paste. Afterwards, 180 mL of deionized water was slowly added into the paste, causing violent effervescence and an increase of temperature up to 98 \\u00b0C. The temperature of the diluted dark brown mixture was kept constant at 98 \\u00b0C for 20 min with vigorous stirring in order to increase the oxidation degree of the GO product. Then 300 ml of warm deionized water was added to further dilute the mixture, which was treated with 30 mL of 30% H2O2, drop by drop within 10 min, in order to reduce the residual permanganate and manganese dioxide to colorless soluble manganese sulfate. The color of the final solution turned to yellow-pale brown. To eliminate the residual metal ions, the filtered cake was washed and filtered four times with warm deionized water and a 10% HCl solution in ethanol and water until the pH reached a neutral level (ca. 6.4). The product was further diluted to approximately 400 mL with deionized water and ultrasonicated at boost mode for 40 min. The yellow-brown GO dispersion was then subjected to dialysis to completely remove metal ions and acids. Finally, it was dehydrated in an air oven at 40 \\u00b0C for 14 h to yield the GO powder. 10 mg of the GO powder was added in 2 mL isopropanol alcohol, then placed in an ultrasonic water bath for 1 h to ensure good exfoliation.\\n\\nA colloidal dispersion of aluminum oxide (Al2O3) nanoparticles [<50 nm particle size (DLS), 20 wt. % in isopropanol] has been used. It was further diluted by sonicating 200 \\u03bcL of this colloidal dispersion in 2 mL isopropanol.\\n\\nFTO-coated glass substrates were cut in pieces of dimensions 1 cm \\u00d7 3 cm. One third of the conductive layer was removed using zinc powder and hydrochloric acid. Then they were washed with mild detergent, rinsed several times with distilled water and subsequently with ethanol and acetone in an ultrasonic bath, finally dried under air stream. A compact thin layer of TiO2 was then deposited on this patterned and cleaned FTO electrode by aerosol spray pyrolysis using a solution of 0.2 M Diisopropoxytitanium bis(acetylacetonate) in EtOH. After spraying, the samples were heated for 1 hour at 500 \\u00b0C. Subsequently, a mesoporous TiO2 layer composed of titania paste made of P25 nanoparticles was spin coated at 4000 rpm for 60 seconds and then dried at 100 \\u00b0C for 20 min and calcined for 30 minutes at 500 \\u00b0C. After that the samples were treated in TiCl4 by dipping into a solution made of 0.04 M TiCl4 in H2O for 30 minutes at 70 \\u00b0C, then copiously rinsing and finally calcining at 500\\u00b0 C. Active perovskite layer was deposited on the thus prepared titania film by the following procedure. A precursor solution was made by mixing 253 mg PbCl2 and 507 mg PbI2 with 270 mg methyl ammonium iodide in a mixture of 1 ml N-N-dimethylformamide (DMF) and 0.5 ml dimethylsulfoxide (DMSO). The solution was kept under stirring for about 2 hours at about 80 \\u00b0C and then deposited by two consecutive spin-coating steps; first 1000 rpm for 10 s, then 6000 rpm for 30 s. During the second step, 1 mL chlorobenzene, as an anti-solvent, was gently dropped on the spinning substrate. The layer was then heated at 90 \\u00b0C for about 45 min, which made the sample\\u2019s color turn from yellow to black. Thereafter, thin mesoporous buffer layers were spin-coated directly on the annealed perovskite layer at room temperature. Both Al2O3 and GO layers were deposited at 2000 rpm for 60 s. The hole transporting material (HTM) was then deposited by spin coating at 3000 rpm for 60s. The HTM solutions were prepared by dissolving 36 mg of HTM powders (spiro-OMeTAD or CuBuPc) in 1 ml of chlorobenzene. In these solutions we added 28.8 \\u03bcL of 4-tert-butylpyridine (TBP) and 17.5 \\u03bcL of a stock solution of Lithium bis (trifluoromethane sulfonyl) imide (Li-TFSI) in acetonitrile (520 mg/1 mL). All of these procedures were carried out under ambient conditions of 50\\u201360% relative humidity. The last step for preparing the solid state solar cell was the deposition of 90 nm thick gold electrodes by thermal evaporation under vacuum. The thickness of the subsequent layers forming the solar cells can be seen in the FESEM cross-sectional image of Fig. 1 . These unit devices had an active size of 15 mm2 (10 mm \\u00d7 1.5 mm) as defined by the size of the gold electrodes.\\n\\nIllumination of the solar cells was made with a PECCELL PEC-L01 Solar Simulator set at 100 mW/cm2, through a mask of aperture size 1 \\u00d7 6 mm2. J\\u2212V characteristic curves were recorded under ambient conditions with a Keithley 2601 source meter that was controlled by Keithley computer software (LabTracer). IPCE values were obtained with an Oriel IQE 200 system. X-ray diffraction (XRD) patterns were obtained with a D8 Advance Bruker diffractometer with Cu K\\u03b1 radiation (\\u03bb = 1.5406 \\u00c5). Absorption and photoluminescence spectra using thin transparent perovskite films were recorded with a Cary 1E UV\\u2013vis spectrophotometer and a Cary Eclipse Fluorescence spectrometer, respectively. FESEM/EDX measurements were made using a Zeiss SUPRA 35VP with a field emission gun equipped with an EDX system (QUANTA 200, Bruker AXS). Electrochemical Impedance Spectroscopy (EIS) characterization has been carried out on PSC devices with a potentiostat/galvanostat (PGSTAT128N, Autolab B.V., Netherlands) under both dark and AM-1.5G illuminated conditions.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | TiCl4,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: CuBuPc,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2, 99.99%, trace metals basis, TCI), lead chloride (PbCl2, purified by sublimation, TCI), methylammonium iodide (MAI, DYESOL company), N, N-dimethyl formamide (DMF, Sigma-Aldrich), dimethyl sulfoxide (DMSO, Sigma-Aldrich) were used as received. Perovskite precursor solutions were prepared by mixing PbI2, PbCl2 and MAI in mixed solvent (DMF: DMSO\\u202f=\\u202f9/1, v/v) at different molar ratio (MAI: PbI2: PbCl2) as following:\\n(3:0:1) (3MAI: 0PbI2: 1PbCl2), (1:1:0) (1MAI: 1PbI2: 0PbCl2), (1:0.8:0.2) (1MAI: 0.8PbI2: 0.2PbCl2), (1:0.9:0.1) (1MAI: 0.9PbI2: 0.1PbCl2), and (1:0.95:0.05) (1MAI: 0.95PbI2: 0.05PbCl2), while maintaining a fixed total concentration of 1.0\\u202fM.\\nThe molar ratio of ([MAI]: [PbI2+PbCl2]) was varied from 0.85\\u00a0to\\u00a01.10 while maintaining a fixed ratio of ([PbCl2]/[PbI2+PbCl2])\\u202f=\\u202f20%.\\n\\nAll Perovskite solar cells were prepared with device configuration of fluorine doped tin oxide (FTO)/compact TiO2/meso-porous TiO2/CH3NH3PbI3-xClx/spiro-OMeTAD/Au under ambient air (humidity, 20% RH) except for the deposition of Au electrode. To define the electrode, the FTO substrate was first etched with Zn powder and 4\\u202fM HCl solution, and then cleaned sequentially by ultrasonication in detergent, acetone and deionized water, respectively, for 15\\u202fmin. The precursor for compact TiO2 was prepared by mixing 0.5\\u202fmL titanium diisopropoxide bis(acetylacetonate) solution with 19.5\\u202fmL anhydrous ethanol. A compact TiO2 (20\\u201330\\u202fnm) film was deposited on FTO substrate by spray pyrolysis of the compact TiO2 precursor at 450\\u202f\\u00b0C. The mesoporous TiO2 was deposited by spin-coating of diluted TiO2 paste (18NRT TiO2 paste: ethanol: terpineol\\u202f=\\u202f1: 2: 4, wt%) at 2500\\u202frpm for 5\\u202fs and 7000\\u202frpm for 60\\u202fs. The spin-coated mesoporous TiO2 layer was dried at 100\\u202f\\u00b0C for 2\\u202fmin and subsequently sintered in an oven at 500\\u202f\\u00b0C overnight. The perovskite precursor solution with designed different component ratio was spin-coated onto mesoporous-TiO2 by two consecutive stages: 1000\\u202frpm for 10\\u202fs and 5000\\u202frpm for 40\\u202fs. And during the high-speed rotation stage, 0.5\\u202fmL toluene was dropped on the center of substrate 30\\u202fs prior to the end of the procedure. Subsequently the resultant perovskite precursor film was annealed at 100\\u202f\\u00b0C for 5\\u202fmin under ambient air (humidity, 20 %RH). From a 40% DMF solution of MAI and PbCl2 (3:1\\u202fM ratio), the perovskite layer was spin-coated on mesoporous TiO2 layer at 2000\\u202frpm for 60\\u202fs. And then it was annealed at 100\\u202f\\u00b0C for 100\\u202fmin and 120\\u202f\\u00b0C for 20\\u202fmin. The HTM solution composed of 72.3\\u202fmg of spiro-OMeTAD in 1\\u202fmL chlorobenzene with 28.5\\u202f\\u03bcL of tert-butylpyridine (t-BP), 8.8\\u202f\\u03bcL of tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) (FK209, 300\\u202fmg\\u202fmL\\u22121 in acetonitrile) and 16.3\\u202f\\u03bcL of tris(bis(trifluoro-methyl-sulfonyl)imide) (Li-TFSI, 520\\u202fmg\\u202fmL\\u22121 in acetonitrile) as additives. The HTM layer was deposited onto perovskite films by spin-coating the HTM solution at 4000\\u202frpm for 30\\u202fs. Finally, 80\\u202fnm of the Au electrode were deposited by thermal evaporation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbI2 (>98%) was from TCI (Japan); HI (48% in water), HCl (57\\u202fwt% in water), Aldrich), CH3NH2 (33\\u202fwt% in absolute ethanol), formamidine acetate (99%), 4-tert-butylpyridine (TBP, 96%), titanium diisopropoxide bis(acetylactonate) in isopropanol (Tiacac, 75%) and Li-bis(trifluoromethanesulfonyl)imide (LiTFSI) were purchased from Sigma-Aldrich. Methylammonium iodide (MAI) and methylammonium chloride (MACl) were synthesized according to the literature. Compounds 1\\u20134 were synthesized according to Refs. .\\n\\n1H and 13C NMR spectra were measured on Bruker 400\\u202fMHz instruments in CDCl3. The melting point was conducted on a SGW-X-4B microscopic melting point apparatus. HRMS spectra were recorded on an Agilent Technologies 1290 Infinity mass spectrophotometer. Scanning electron microscopy (SEM, Sirion200, Holland Fei) was performed to observe the film morphology. Time-resolved luminescence decays were recorded with time-correlated single photo counting system (PicoHarp 300, PicoQuant GmbH). The excitation light source was Ti:Sapphire laser (Mira 900, Coherent; 76\\u202fMHz, 130\\u202ffs). UV\\u2013vis absorption spectra of molecules were measured on Shimadzu UV-2450 spectrophotometer. The emission spectra of the molecules in THF solution were performed on a Fluorolog III photoluminescence. Cyclic voltammetry (CV) measurements were recorded on a CHI660E electrochemical workstation using a typical three electrode electrochemical cell in a solution of tetrabutylammonium hexafluorophosphate (TBAPF6) in dry MeCN with a scan rate of 50\\u202fmV\\u202fs\\u22121, an Ag/AgCl electrode as the reference electrode and a platinum wire as the counter electrode. The ferrocene/ferrocenium (Fc/Fc+) redox couple acted as an internal potential reference.\\n\\nThe patterned ITO coated glass was ultrasonically cleaned with detergent water, deionized water, acetone and ethanol continuously. The substrate was treated with UV-O3 for 20\\u202fmin. In brief, a 50\\u202fnm-thick compact TiO2 layer was deposited onto the ITO substrate with 3000\\u202frpm twice followed by 150\\u202f\\u00b0C annealing 30\\u202fmin. After cooling to room temperature, CH3NH3PbI3Cl3-x film was prepared via a modified two-step solution process , where PbI2 (450\\u202fmg\\u202fmL\\u22121 dissolved in dimethyl formamide) was spin-coated on top of electron transporting layer (ETL) at 2500\\u202frpm for 30\\u202fs and CH3NH3I (50\\u202fmg\\u202fmL\\u22121 with CH3NH3Cl of 10:1 in weight ratio comparing to CH3NH3I dissolved in 2-propanol) was spin coated on top of the dried PbI2 layer at room temperature at 3000\\u202frpm for 30\\u202fs. The films were annealed at 135\\u202f\\u00b0C for 3\\u20135\\u202fmin. A HTL was coated on the perovskite film at 3000\\u202frpm for 30\\u202fs. The HTL solution contains 20\\u202fmg of TPADPP-1, TPADPP-2 or PTZDPP-2, 28.8\\u202f\\u03bcL of TBP, 17.5\\u202f\\u03bcL of Li-TFSI/acetonitrile (520\\u202fmg\\u202fmL\\u22121) per 1\\u202fmL chlorobenzene. Finally, an 80\\u202fnm gold counter electrode was deposited by thermal evaporation. The thickness of each layer was 50\\u202fnm for TiO2 ETL, 350\\u202fnm for perovskite layer, 200\\u202fnm for spiro-OMATD HTL, and 80\\u202fnm for gold electrode.\\nA xenon light source solar simulator (450\\u202fW, Oriel, model 9119) with an AM 1.5G filter (Oriel, model 91192) was used to give an irradiance of 100\\u202fmW\\u202fcm\\u22122 at the surface of the solar cells. The photocurrent\\u2013voltage (J\\u2013V) characteristics of the MAPbI3 \\u2212 xClx-based solar cells were measured by recording the current through Keithley 2400 digital source meter. The devices were tested using a metal mask with an area of 0.108\\u202fcm\\u22122. A similar data-acquisition system was used to control the incident photon conversion efficiency (IPCE) measurements. No white-light bias was applied onto the sample during the IPCE measurements with the direct current (DC) model (Fig. 2 ).\\n\\nInto a solution of compound 1 (308\\u202fmg, 0.54\\u202fmmol), compound 2 (150\\u202fmg, 0.225\\u202fmmol) and 2\\u202fmol\\u202fL\\u22121 aqueous Na2CO3 solution (6\\u202fmL) in toluene, two drops of aliquat@366, Pd(PPh3)4 (200\\u202fmg) was added as a catalyst. The reaction mixture was stirred under argon atmosphere at 90\\u202f\\u00b0C for 12\\u202fh. After cooling to room temperature, the reaction was quenched by water and the mixture was extracted with CH2Cl2. The organic layer was dried over MgSO4 and evaporated by reduced pressure. The residue was purified by column chromatography on silica gel column. TPADPP-1 was a red solid of M.p. 87\\u201390\\u202f\\u00b0C. 1H NMR (400\\u202fMHz, CDCl3): \\u03b4 7.90 (d, J\\u202f=\\u202f8.4\\u202fHz, 4H), 7.71 (d, J\\u202f=\\u202f8.4\\u202fHz, 4H), 7.48 (d, J\\u202f=\\u202f8.4\\u202fHz, 4H), 7.11\\u20137.09 (m, 8H), 7.00 (d, J\\u202f=\\u202f8.4\\u202fHz, 4H), 6.87\\u20136.85 (m, 8H), 3.96 (t, J\\u202f=\\u202f6.6\\u202fHz, 8H), 3.82 (t, J\\u202f=\\u202f7.4\\u202fHz, 4H), 1.83\\u20131.76 (m, 8H), 1.68\\u20131.63 (m, 4H), 1.52\\u20131.45 (m, 8H), 1.38\\u20131.34 (m, 16H), 1.27\\u20131.22 (m, 22H), 0.94\\u20130.88 (t, J\\u202f=\\u202f6.8\\u202fHz, 12H), 0.85 (t, J\\u202f=\\u202f6.8\\u202fHz, 6H). 13C NMR (100\\u202fMHz, CDCl3): \\u03b4 162.9, 155.8, 149.0, 148.0, 143.4, 140.4, 131.1, 129.3, 127.5, 126.9, 126.9, 126.5, 126.1, 120.1, 115.4, 109.8, 68.3, 31.8, 31.6, 29.5, 29.4, 29.1, 29.1, 26.8, 25.8, 22.6, 14.1, 14.0. HRMS (ESI, m/z): [M\\u202f+\\u202fNa]+ calcd for C94H118N4NaO6: 1421.8944. Found: 1421.8929.\\nThe synthesis method of TPADPP-2 was similar to that of TPADPP-1, except compound 3 instead of 2. TPADPP-2 was a purple solid of M.p. 154\\u2013157\\u202f\\u00b0C. 1H NMR (400\\u202fMHz, CDCl3): \\u03b4 8.97 (d, J\\u202f=\\u202f4.4\\u202fHz, 2H), 7.46 (d, J\\u202f=\\u202f8.8\\u202fHz, 4H), 7.31 (d, J\\u202f=\\u202f4.4\\u202fHz, 2H), 7.08\\u20137.06 (m, 8H), 6.90 (d, J\\u202f=\\u202f8.8\\u202fHz, 4H), 6.86\\u20136.83 (m, 8H), 4.10 (t, J\\u202f=\\u202f7.6\\u202fHz, 4H), 3.94 (t, J\\u202f=\\u202f6.6\\u202fHz, 8H), 1.82\\u20131.74 (m, 12H), 1.50\\u20131.42 (m, 12H), 1.39\\u20131.33 (m, 20H), 1.27\\u20131.25 (m, 12H), 0.92 (t, J\\u202f=\\u202f7.0\\u202fHz, 12H), 0.85 (t, J\\u202f=\\u202f6.8\\u202fHz, 6H). 13C NMR (100\\u202fMHz, CDCl3): \\u03b4 161.4, 156.0, 150.4, 149.5, 139.9, 139.1, 136.9, 127.3, 127.1, 127.1, 126.8, 124.6, 123.0, 119.6, 115.4, 107.6, 68.3, 31.8, 31.6, 30.0, 29.3, 29.2, 26.9, 25.8, 22.6, 14.1, 14.0. HRMS (ESI, m/z): [M+Na]+ calcd for C90H114N4NaO6S2: 1433.8072. Found: 1433.8032.\\nThe synthesis method of PTZDPP-2 was similar to that of TPADPP-2, except compound 4 instead of 1. PTZDPP-2 was obtained as a purple solid. M.p. 150\\u2013153\\u202f\\u00b0C. 1H NMR (400\\u202fMHz, CDCl3) \\u03b4 8.92 (d, J\\u202f=\\u202f3.6\\u202fHz, 2H), 7.43\\u20137.38 (m, 4H), 7.31 (d, J\\u202f=\\u202f3.6\\u202fHz, 2H), 7.17\\u20137.12 (m, 4H), 6.93 (t, J\\u202f=\\u202f7.4\\u202fHz, 2H), 6.86\\u20136.80 (m, 4H), 4.09 (t, J\\u202f=\\u202f6.8\\u202fHz, 4H), 3.83 (t, J\\u202f=\\u202f6.4\\u202fHz, 4H), 1.80\\u20131.77 (m, 8H), 1.45\\u20131.29 (m, 40H), 0.88 (m, 12H). 13C NMR (100\\u202fMHz, CDCl3) \\u03b4 161.7, 148.8, 145.7, 144.5, 139.6, 136.9, 128.7, 127.5, 127.5, 127.4, 125.5, 125.5, 125.2, 124.6, 123.9, 123.5, 122.8, 115.5, 115.5, 108.0, 47.7, 46.0, 39.3, 31.8, 30.4, 29.2, 28.6, 26.9, 26.8, 23.7, 23.2, 22.6, 14.1, 14.1, 10.6, 1.0. HRMS (ESI, m/z): [M\\u202f+\\u202fNa]+ calcd for C70H86N4NaO2S4: 1165.5526. Found: 1165.5515.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 135.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 5.0,\\n HTL_stack_sequence: TPADPP-1,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.108,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were used without further purification. Er2O3 (99.99%), Yb2O3 (99.99%), Y2O3 (99.99%) and Na2CO3 (99.99%) trifluoroacetic acid (CF3COOH, 99.5%), oleylamine (OAm, C18: 80\\u201390%), n-hexane (98%), were purchased from Aladdin. NOBF4 (95%) and PbI2 (99.9985%) were purchased from Alfa Aesar. The CH3NH3I (>99%) and 2,29,7,70-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,99- spirobifluorene (Spiro-MeOTAD) (>99%) were obtained from Dyesol. Lithium bis(trifluoromethanesulfonyl) imide (Li-TFSI, 99.95%), acetonirtile (99.8%), 4-tert-butylpyridine (TBP, 96%) were purchased from Sigma-Aldrich. All other organic solvents were obtained as analytical grade from J&K Chemical Ltd. with storage in seal bottle with molecular sieves.\\n\\n\\u03b2-NaYF4:Yb, Er UCNCs were synthesized according to the method reported in the literature . Typically, CF3COONa, Y(CF3COO)3, Yb(CF3COO)3, and Er(CF3COO)3 were synthesized by dissolving Na2CO3, Y2O3, Yb2O3, and Er2O3 in 50\\u00a0vol% trifluoroacetic acid aqueous solution with reflux at 80\\u00a0\\u00b0C for 6\\u00a0h. Then, a mixture of Er(CF3COO)3 (0.04\\u00a0mmol), Yb(CF3COO)3 (0.40\\u00a0mmol), Y(CF3COO)3 (1.56\\u00a0mmol), CF3COONa (4\\u00a0mmol) was dissolved in 30\\u00a0mL oleylamine, and heated to 100\\u00a0\\u00b0C at reduced pressure for 30\\u00a0min to remove H2O and O2 and subsequently heated at 330\\u00a0\\u00b0C for 1\\u00a0h under argon atmosphere. After naturally cooled to 80\\u00a0\\u00b0C, the UCNCs was obtained by centrifugation, rinsing with ethanol, and finally dispersed in 10\\u00a0mL n-hexane for further uses.\\n\\nOAm ligands on the UCNCs surface were removed using a NOBF4-mediated ligand-exchange approach . Typically, n-hexane solution of OAm-UCNCs (20\\u00a0mg\\u00a0mL\\u22121) was mixed anhydrous DMF solution of NOBF4, and then shaken gently for 10\\u00a0min to get rid of OAm ligands. The BF4 \\u2212-capped UCNCs was collected from the export of the separatory funnel and then re-dispersed in DMF. BF4 \\u2212-UCNCs in DMF (20\\u00a0mg\\u00a0mL\\u22121) and DMF solution of IR806 dye (1\\u00a0mg\\u00a0mL\\u22121) were mixed and kept for overnight at room temperature to graft IR806 on the surface of UCNCs. After rinsed by toluene and isopropanol (1:1 v/v) and centrifuged, IR806-UCNCs was re-dispersed in DMF (60\\u00a0mg\\u00a0mL\\u22121) for further use.\\n\\nA x \\u03bcL (x\\u00a0=\\u00a050, 100, 150 or 200) of IR806-UCNCs solution in DMF was mixed with (1000\\u2013X) \\u03bcL of perovskite precursor (163\\u00a0mg MAI and 470\\u00a0mg PbI2 in DMF) to obtain IR806-UCNCs-mixed perovskite precursor solution. The indium tin oxide (ITO)-coated glass substrates (Dyesol) (Xiang Sci. Tech. Co., 8\\u00a0\\u03a9\\u00a0m\\u22122) was cleaned successively with acetone, detergent, deionized water, and isopropanol, and finally treated under oxygen plasma for 20\\u00a0min to remove the last trace of organic residues. Compact ZnO layer was deposited onto Glass/ITO by spin-coating [Zn(NH3)4](OH)2 on the ITO/glass substrate under 2000\\u00a0rpm for 30s, followed by annealing at 150\\u00a0\\u00b0C for 10\\u00a0min. The perovskite precursor solution was then spin-coated on the ZnO compact layer at 5000\\u00a0rpm for 30\\u00a0s and 0.1\\u00a0mL of chlorobenzene was quickly dripped on the rotating substrate in the 6th second since spinning before the surface changed to be turbid caused by rapid vaporization of DMF. After being heated at 70\\u00a0\\u00b0C for 20\\u00a0min, the CH3NH3PbI3-based ZnO films was covered with the hole transport material (HTM) consisting of 72.3\\u00a0mg Spiro-MeOTAD, 17.5\\u00a0\\u03bcL Li-TFSI/acetonitrile (520\\u00a0mg\\u00a0mL\\u22121) and 28.8\\u00a0\\u03bcL 4-TBP in a solvent of 1\\u00a0mL chlorobenzene via spin-coating at 2500\\u00a0rpm for 30\\u00a0s. Finally, PSC device assembly was completed by thermal evaporation of a 70\\u00a0nm thick Ag as the counter electrode onto the top of the HTM layer.\\n\\nTransmission electron microscopy (TEM) image was captured using Hitachi 7700 microscope. The morphology of perovskite films and cross sectional view of PSCs were observed on a scanning electron microscope (SEM, JEOL-6701F). The crystal structure of \\u03b2-NaYF4:Yb, Er and perovskite films was examined in 2\\u03b8 range from 10\\u00b0 to 60\\u00b0 with CuKR radiation (\\u03bb\\u00a0=\\u00a00.15406\\u00a0nm) operated at 40\\u00a0mA and 40\\u00a0kV using an X-ray diffractometer (XRD, Rigaku, D/max 2500 VB2\\u00fe/PC). The upconversion photoluminescence (PL) spectra were performed on a spectrophotometer (FLS980, Edinburgh) with a CW NIR laser at 980\\u00a0nm and 808\\u00a0nm as the excitation source, respectively. Absorption spectra of IR806 dyes, colloidal nanoparticles, as well as IR806-UCNCs dispersed in DMF and perovskite films were acquired using by a UV-Vis-NIR light absorption spectrometry (Lambda 950, Perkin Elmer). The Fourier transform infrared (FT-IR) spectra was recorded by a FT-IR spectroscopy (Vertex 70 v, Bruker) in the 4000\\u2212650\\u00a0cm\\u22121 range. The KBr powder (99.999%, PIKE Tech) was used for the powdered samples. Atomic force microscopy (AFM) height images were characterized with a Bruker Metrology Nanoscope III-D atomic force microscope in tapping mode. Photovoltaic performances of PSCs were characterized by measuring the current-voltage curves under AM 1.5G sunlight with 100\\u00a0mW\\u00a0cm\\u22122 light output using a solar light simulator (Newport Oriel Sol 3A class, America, calibrated by a Newport reference cell), and the data were recorded with a Keithley 2400 source meter from 1.5\\u00a0V to - 0.5\\u00a0V with a scan rate of 0.2\\u00a0V\\u00a0s\\u22121 and a pre-condition of 0.5\\u00a0s. The NIR response of the PSC devices were tested under AM 1.5G sunlight with a 780\\u00a0nm high-pass optical filter on the light path. EQE was acquired by an Oriel model QE-PV-SI system equipped an irradiation of 300\\u00a0W Xe lamp together with a calibrated silicon photodetector. Steady state PL spectra (SS-PL) was characterized at 775\\u00a0nm after excited at 470\\u00a0nm with a Xenon lamp. Time-resolved PL spectra (TR-PL) was measured on PL spectrometer (FLS 980, Edinburgh Instruments), excited with a picosecond pulsed diode laser CW NIR laser at 460\\u00a0nm as the excitation source and measured at 775\\u00a0nm. The TR-PL decay curves were fitted with a tri-exponential function as PL intensity\\u00a0=\\u00a0A\\u00a0+\\u00a0\\u03a3Biexp (\\u2212t/\\u03c4i), and the relative content (Ai) of each time constant \\u03c4 was calculated by Ai\\u00a0=\\u00a0Bi\\u03c4i/(\\u03a3Bi\\u03c4i). The electrochemical impedance spectroscopy (EIS) measurements was performed by Zennium electrochemical workstation illuminated under AM 1.5G, and the EIS Nyquist plots were measured at a bias of 0.8\\u00a0V with AC amplitude of 10\\u00a0mV under a frequency ranging from 0.1 to 105\\u00a0Hz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: NaYF4:Tb:Er-np,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless noted otherwise, all materials were purchased from Sigma Aldrich without further purification. PbI2 (99.9985%), N,N-Dimethylformamide (99.8%), di-iodomethane (99%), and SnO2 solution (15% in H2O colloidal dispersion) were purchased from Alfa Aesar. Methylammonium iodide (MAI), Formamidinium iodide (FAI), and cobalt dopant FK209 were purchased from Greatcell solar. The 2,20,7,70-Tetrakis(N,N-di-p-methoxyphenylamine)-9,90-spirobi\\ufb02uorene (Spiro-MeOTAD) was acquired from Merck. FTO glass substrates (<20\\u202f\\u03a9/sq., 2\\u202fcm\\u202f\\u00d7\\u202f2\\u202fcm\\u202f\\u00d7\\u202f3\\u202fmm) and gold palettes (99.999%) were purchased from Hartford glass and Kurt J. Lesker Co., respectively. ITO coated PET sheets (60\\u202f\\u03a9/sq.) were purchased from Sigma Aldrich.\\n\\nFTO/ITO coated slides (2\\u202fcm\\u202f\\u00d7\\u202f2\\u202fcm) were initially etched using zinc powder and 2\\u202fM HCl and were subsequently cleaned through sequential sonication in a 1:10\\u202f V/V diluted solution of Hellmanex detergent in DI water, DI water, ethanol, and DI water for 10\\u202f minutes each. After blowing with nitrogen to remove the remainder water, 20 \\u202fminutes plasma treatment was applied to the cleaned substrates to improve the surface energy and thus the hydrophilicity. The SnO2 ETL was then spin coated from a 1:4 \\u202fV/V diluted solution of the SnO2 colloidal dispersion in fresh DI water using the spinning rate of 2000\\u202f rpm for 30 \\u202fseconds. Before annealing, the coated electrode places were wiped off with cotton swabs dipped in DI water. The substrates were immediately transferred to the IPL machine to perform the annealing process using different flash counts having different energy quantities and were later put under a UV lamp to provide surface treatment and remove the organic contaminants for 15\\u202fmin. The perovskite ink was then passed through a 0.45\\u202f\\u03bcm PTFE syringe filter and spin-coated on the SnO2 coated substrates at two consecutive spinning rates of 1000\\u202frpm for 10\\u202fs and 3000\\u202frpm for 30\\u202fs. During the last 12\\u202fs of the spinning process, 200\\u202f\\u03bcL of chlorobenzene solution was pipetted on the rotating substrate to take the solution to the supersaturation mode and form a transparent yellow wet film. The Cs0.05(MA0.85FA0.15)0.95PbI3 triple cation perovskite ink was made in a nitrogen filled glovebox in compliance to our previous ink engineering stated elsewhere []. In brief, 0.013 gr CsI, 0.6454 gr PbI2, 0.0343 gr FAI, and 0.18 gr MAI was initially dissolved in 1\\u202fmL DMF and 0.125\\u202fmL DMSO. After complete dissolution and the formation of a transparent yellow solution, 0.25\\u202fmL di-iodomethane was pipetted to the solution and stirred for 2\\u202f hours to provide the complete dissolution. During the spinning process, a dry air stream was put in the spin coater chamber to keep the relative humidity less than 10%. After heating the wet perovskite film for 20 \\u202fseconds on a hotplate at 110\\u202f\\u00b0C, the slides were immediately taken to the IPL machine to perform rapid perovskite annealing through 5 pulses, each with 1.4\\u202fkJ energy. For flexible substrates, the wet film coated sheets were placed on a hotplate at 75\\u202f\\u00b0C for 10\\u202fs to form a dark brown film and were subsequently sintered through a single IPL shot with 900\\u202fJ energy, an optimal condition where perovskite film damage was observed at higher energy quantities. Both hotplate and IPL annealing steps were carried out in the ambient with relative humidity of 60%. Right after perovskite annealing, the substrates were transferred to a nitrogen filled glovebox for the Spiro-MeOTAD hole-transport layer deposition. The Spiro-MeOTAD solution was made by initially dissolving a 72.3\\u202fmg of Spiro-MeOTAD in 1mL chlorobenzene. 28.8\\u202f\\u03bcL 4-tert-butyl-pyridine was then pipetted to the solution and mixed. Later, a 17.5\\u202f\\u03bcL of a stock solution of 520 \\u202fmg/mL lithium bis (trifluoromethylsulphonyl) imide in anhydrous acetonitrile was pipetted to the solution and stirred until full dissolution. Finally, 29\\u202f\\u03bcL of the cobalt dopant FK209 TFSI salt (300\\u202f mg/mL in anhydrous acetonitrile) was pipetted to the mixture to prepare the final solution. The Spiro-MeOTAD film was made by spin-coating 70\\u202f\\u03bcL of the prepared solution at 1700 \\u202frpm for 30 \\u202fseconds. Ultimately, an 80\\u202fnm gold electrode was deposited through a thermal evaporator.\\n\\nXRD measurements were carried out within the 2\\u03b8 range between 10\\u00b0 and 60\\u00b0 using a Bruker AXS D8 X-ray Diffractometer equipped with a position sensitive detector (PCD) and an X-ray source of CuK\\u03b1 (\\u03bb\\u202f=\\u202f0.1548\\u202fnm) with the scanning speed of 1 Sec/Step and the step size of 0.02\\u00b0. IPL annealing was done through a Xenon S-2000 rack-mounted sintering system with linear Xenon flash lamp placed within 5.7\\u202fcm from the substrates. Surface morphology inspections were done through a FEI Nova NanoSEM 600 SEM machine with an accelerating voltage of 10\\u202fkV and a working distance of 5\\u202fmm. The impedance spectroscopy (IS) and the current-voltage curves were obtained using an Autolab PGSTAT128-N potentiostat with the scanning rate of 0.1\\u202f V/Sec. Each cell was illuminated from the back side with an active area of 0.12\\u202f cm2 using an AM 1.5 simulated light from a Newport LCS-100 solar simulator. The transmission and absorption spectra were obtained using PerkinElmer Lambda 950 UV\\u2013Vis spectrometer between 250 and 800\\u202fnm wavelengths. PL analysis was carried out using a Renishaw inVia Raman microscope with a CCD detector and a 632\\u202fnm He\\u2212Ne laser source. X-ray photoelectron spectroscopy (XPS) data was obtained from VG scientific MultiLab 3000 under ultrahigh vacuum pressure range within 10\\u22128\\u202fTorr using an Mgk\\u03b1 radiation X-ray source (h\\u03bd\\u202f>\\u202f1253.6\\u202feV) with respect to the carbon C1S peak position.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.15MA0.85PbI3,\\n Perovskite_composition_short_form: CsFAMAPbI,\\n Perovskite_additives_compounds: di-iodomethane,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 110,\\n Perovskite_deposition_thermal_annealing_time: 0.3,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Both of PbI2 and PbBr2 were purchased from Aldrich-Sigma (99.9985%); methylammonium bromide (MABr), methylammonium iodide (MAI) and formamidinium iodide (FAI) were obtained from Shanghai Materwin New Materials Co., Ltd. N, N-Dimethylformamide (DMF), dimethylsulfoxide (DMSO), polystyrene (PS) and chlorobenzene were from Alfar Aesar. Spiro-OMeTAD was from Luminescence Technology Corp. All the chemicals were directly used without further purification. Laser-patterned FTO glass (Pilkington, thickness of 2.2 mm and sheet resistance of 15 \\u03a9 sq\\u22121) was sequentially cleaned with a mild detergent, distilled water and ethanol in an ultrasonic bath. The substrate was treated with UV-ozone for 15 min prior to use.\\n\\nThe mixture solution was prepared by dissolving different molar quantities of 1.32 M PbI2, 1.08 M FAI, 0.12 M PbBr2, 0.24 M MAI and 0.12 M MABr in 1 L solvent of N, N-Dimethylformamide (DMF) and dimethylsulfoxide (DMSO) at a volume ration of 4:1. The solution was stirred for 6 h at room temperature. In addition, the chlorobenzene solution of polystyrene (PS) was prepared by dissolving different concentration PS (0 mg ml\\u22121, 1 mg ml\\u22121, 2.5 mg ml\\u22121, 5 mg ml\\u22121, 10 mg ml\\u22121, 20 mg ml\\u22121) into chlorobenzene and stirred until completely dissolved at room temperature.\\n\\nThe compact TiO2 blocking layer about 30 nm was deposited onto the FTO substrate by spin coating (at a speed of 3000 rpm) a sol-gel precursor solution consisting of 0.125 M L\\u22121 titanium isopropoxide and 0.125 M L\\u22121 HCl in n-butylalcohol and sintering at 500 \\u00b0C for 1 h. After cooling down to room temperature, the TiO2 film was treated with 0.025 M L\\u22121 TiCl4 aqueous solution for 30 min, then sintering at 500 \\u00b0C for 1 h. The perovskte films were fabricated by an anti-solvent one-step spin-coating method. Perovskite precursor solution was dropped onto TiO2 blocking-layer and spin-coated at 1000 rpm for 10 s and 5000 rpm for 30 s 120 \\u00b5l solution of different concentrations of PS was poured onto the spinning substrate at 15 s during the high speed stage. Then the half-crystallization film was heated at 150 \\u00b0C in N2 atmosphere for 10 min and 100 \\u00b0C in vacuum for 40 min. Spiro-OMeTAD layer with a thickness of about 200 nm was spin coated onto the top of perovskite film at a speed of 3000 rpm and then heated for 5 min at 60 \\u00b0C on a hot plate in glovebox. At last, Au electrode about 80 nm was deposited via thermal evaporation under the vacuum of 10\\u22127 Torr.\\n\\nSEM images of perovskite film were measured by scanning electron microscopy (SEM, Hitachi S4800). The measurement conditions were 10 kV at various magnifications, as shown on the data bar of the images. X-Ray Diffraction (XRD) was measured on a Bruker X-ray diffractometer using Cu Ka as the radiation source. Contact angles were measured by OCA25, DataPhysics. Dosing volume of water was 2 \\u00b5l with 0.5 \\u00b5l s\\u22121 dosing rate. Absorption spectra were measured on SHIMADZU UV-2550 from 860 to 350 nm. Constant temperature and humidity decay measurement was obtained under T = 30 \\u00b0C, RH = 80% by constant temperature and humidity chamber (KCL-1000) purchased from EYELA. I-V results were measured under AM 1.5 simulated sunlight (100 mW cm\\u22122) from Zolix SS150A, which was recorded by a digital source meter (Keithley model 2602). The solar cells devices were masked with a black aperture to define the active area of 0.1 cm2. Scan range was from \\u22120.05 to 1.2 V for forward scan and from 1.2 V to \\u22120.05 V for reverse scan. The speed of scan was 30 mv s\\u22121 for a delay time of 0.3 s. External quantum efficiency (EQE) of the devices was measured with a lab-made setup under 0.3\\u20130.9 mW cm\\u22122 monochromic light illumination without bias illumination.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: TiCl4,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.75MA0.25PbBr0.25I2.75,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150.0; 100.0,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 40.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 30.0; 30.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 60,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 48,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbBr2 (99.99%, TCI), Cesium iodide (CsI, TCI), anhydrous N, N-dimethylformamide (DMF, 99.99%, Sigma-Aldrich), Poly (3-hexylthiophene-2,5-diyl) (P3HT), Potassium hydroxide (KOH), Carbon disulfide (CS2), Phenethyl alcohol. ITO glass, SnO2 nanoparticles (15% dispersed in H2O), Tin (II) chloride (SnCl2) which are purchased without any further purification.\\n\\n5\\u2009ml distilled water was added in 25\\u2009ml tetrahydrofuran containing 1.12\\u2009g potassium hydroxide (KOH, 20\\u2009mmol). Phenethyl alcohol (20\\u2009mmol, 2.44\\u2009g) was put into the mixed solution, carbon disulfide (30\\u2009mmol, 2.28\\u2009g) was added dropwise to the solution about 15\\u2009min after stirring for another 1\\u2009h. The obtained crude products was washed with ethanol and ether consecutively to obtain potassium phenethyl xanthate after the evaporation of solvent. Then cesium bromide (10\\u2009mmol, 2.13\\u2009g) was dissolved in distilled water completely, synthesized potassium phenethyl xanthate was added in above solution, after the mixture was stirred for 3\\u2009h, the yellow precipitate was filtered and washed by ethanol 3 times. Finally, resultant powder was dried in vacuum for 24\\u2009h.\\n\\nITO glasses were sonicated with distilled water, acetone and isopropanol sequentially for 15\\u2009min in each solvent, 15\\u2009min UV-O3 treatment was further performed on ITO substrates prior to the deposition of SnO2 compact layer. Diluted SnO2 colloid solution (2.67% in water) was spin-coated on ITO substrates with 2000\\u2009rpm for 30\\u2009s and then annealed at 150\\u2009\\u00b0C for 30\\u2009min, then SnCl2 solution (0.1\\u2009M in ethanol) was spin-coated on SnO2 compact layer with 6000\\u2009rpm for 30\\u2009s and annealed at 180\\u2009\\u00b0C for 1\\u2009h. CsPbIBr2 perovskite precursor solution was prepared through mixing CsI (1.35\\u2009M) and PbBr2 (1.35\\u2009M) in pure DMSO solvent. For CsXth in perovskite solution, 2.5%, 5% and 10% M/M CsXth was dissolved in CsPbIBr2 precursor respectively. All-inorganic perovskite film was fabricated by spin-coating 75\\u2009\\u03bcl perovskite precursor solution at 1000\\u2009rpm for 20\\u2009s and 3000\\u2009rpm for 30\\u2009s, 500\\u2009\\u03bcl ethyl acetate was dropped quickly onto the film at the last 10\\u2009s during the second step. Then the film was annealed on hotplate at 160\\u2009\\u00b0C for 10\\u2009min, for CsXth in perovskite, the film was annealed on hotplate at 160\\u2009\\u00b0C for 5\\u2009min and increased to 230\\u2009\\u00b0C slowly and annealed for 10\\u2009min in inert atmosphere. After cooling down to room temperature, P3HT solution (10\\u2009mg/ml in chlorobenzene) was spin-coated at 3000\\u2009rpm for 30\\u2009s and annealed at 160\\u2009\\u00b0C for 10\\u2009min. Finally, 80\\u2009nm gold was evaporated as electrode under high vacuum (<\\u20094\\u2009\\u00d7\\u200910\\u22123 Pa).\\n\\nPerovskite film morphology was performed by SEM (HITACHI S4800). The current density-voltage characteristics of solar cells were conducted under AM 1.5G simulated solar illumination, the active area of each solar cell was 0.10\\u2009cm2 during the test. The external quantum efficiencies were measured by illuminating solar cells under monochromatic light from 900\\u2009nm to 300\\u2009nm (300\\u2009W Xenon lamp with a monochromator, Newport 74010). The EQE was performed by under monochromatic light from 800\\u2009nm to 300\\u2009nm (300\\u2009W Xenon lamp with a monochromator, Newport 74010). Transform Infrared Spectroscopy (FTIR) measurement was conducted using JASCO FTIR 4100 in transmission mode. XRD pattern was analyzed by D8 X-ray diffractometer, using Cu K\\u0251 radiation. The steady-state photoluminescence (PL) and timed-resolved PL measurement was obtained by the Fluorolog-3-p spectrophotometer by excitation light. X-ray photoelectron spectroscopy (XPS) system with Thermo Scientific and C1s binding energy at 284.8 ev as the referenced was applied, ESCLAB 250Xi was used to measure the binding energy of Pb4f, Cs3d, Br3d and S2p element. Electrochemical impedance spectra was measured by an electrochemical workstation (Parstat 2273, Princeton) under 0.6\\u2009V positive bias. FTIR for perovskite thin films was measured using PRO400-S mode. Thermogravimetric analysis (TGA) was conducted in nitrogen atmosphere at a temperature rate of 10\\u2009\\u00b0C per min.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: SnCl2,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBr2I,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 160; 230,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 10.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25.0; 25.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 2,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Indium tin oxide (ITO) coated glass substrates with a sheet resistance of 8\\u00a0\\u03a9/sq and ITO thickness of 180\\u00a0nm were purchased from Huayulianhe Co., Ltd. Ammonia solution (25\\u201328%), PEDOT:PSS (Clevious P VP AI 4083), PbI2 (99.9985%), C60 (99.9%) and 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) (99.9%) were purchased from Sinopharm Chemical Reagent Co., Ltd, H. C. Stark Company, Alfa Aesar, Puyang Yongxin Fullerene Technology Co., Ltd and Xi'an Polymer Light Technology Corp. (PLT), respectively. Methylammonium iodide (CH3NH3I) was synthesized according to the procedure reported previously. The perovskite precursor solution (43\\u00a0wt%) was prepared by mixing the PbI2, PbCl2 and CH3NH3I (10:1:11 molar ratio) in anhydrous N,N-dimethylformamide (DMF) and stirring until to produce a clear and transparent CH3NH3PbI3-xClx solution. All these commercially available materials were used as received without any further purification.\\n\\nThe ITO coated glass substrates were cleaned ultrasonically in detergent, deionized water, acetone and isopropyl alcohol sequentially and ultraviolet-ozone treated for 10\\u00a0min. The ammonia-doped PEDOT:PSS aqueous solutions were prepared by adding different ratio of ammonia (the volume ratio of ammonia was 0, 2%, 4%, 6%, 8%) and then treated by ultrasonic for 30\\u00a0min. The PEDOT:PSS films (40\\u00a0nm) were deposited by spin-coating at 500\\u00a0rpm for 9\\u00a0s and at 4000\\u00a0rpm for 60\\u00a0s using PEDOT:PSS solutions which were filtered through a 0.45\\u00a0\\u03bcm filter before use. Subsequently, the PEDOT:PSS films were transferred to a glove box and baked at 140\\u00a0\\u00b0C for 20\\u00a0min on a heating stage. After cooling to room temperature, the perovskite percursor solution was dropped onto the different modified PEDOT:PSS HTLs and spin-coated with a speed of 5000\\u00a0rpm for 60\\u00a0s. After 5\\u00a0s of spin-coating the perovskite solution, a 200\\u00a0\\u03bcL anhydrous chlorobenzene was quickly dropped onto the center of the substrate. The pristine perovskite films were annealed at 80\\u00a0\\u00b0C for 10\\u00a0min. Finally, C60 (40\\u00a0nm), BCP (8\\u00a0nm) and Ag (100\\u00a0nm) layers were sequentially deposited on the CH3NH3PbI3-xClx film by thermal evaporation under vacuum (10\\u22126\\u00a0mbar). The active area of the devices was 0.100\\u00a0cm2.\\nAll measurements of photovoltaic performance were performed in a glove box. The current density-voltage curves of perovskite solar cells were measured under 100\\u00a0mW/cm2 AM 1.5G simulated illumination using a Keithley 4200 Semiconductor Characterization System with an Oriel 300\\u00a0W solar simulator (Thermo Oriel 91160-1000) as an excitation source. Scanning electron microscope (SEM) and atomic force microscope (AFM) images were collected on a Hitachi S-4800 and SPI3800/SPA400 SPM (Seiko Instrument Inc), respectively. The thickness of the thin films was measured with a KLA-Tencor Alpha-Step Surface Profiler. The work function of PEDOT:PSS films were measured by using ultraviolet photoelectron yield spectroscopy (Riken Keiki). The time-resolved photoluminescence (PL) measurements were carried out by a combined fluorescence lifetime and steady state spectrometer (FLS980, Edinburgh Instruments Ltd.). The crystallographic properties of CH3NH3PbI3-xClx films on the ITO/PEDOT:PSS substrates were investigated using a D/MAX-2000 X-ray diffractometer with monochromated Cu K\\u03b1 irradiation (\\u03bb\\u00a0=\\u00a01.5418\\u00a0\\u00c5) at a scan rate of 4\\u00b0 min\\u22121. If no otherwise specified, the ammonia-doped PEDOT:PSS films for characterization and device fabrication were prepared under the optimal volume ratio of 4%.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: NH3,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A series of luminescent materials were evaluated from a previous study according to an optimization process reported by Fernandes et\\u00a0al. . These included a range of 10 LDS materials, from metal complexes to organic dyes. The relevant aspects to considering the LDS application of the materials were their optical properties, processability, commercial availability and cheapness. The material selected for this work was Kremer fluorescent blue (KB), which is based upon a Triazine-toluene sulfonamide-paraformaldehyde-based resin. The LDS material was dissolved with PMMA into anisole at a concentration of 8% by weight. The layers were deposited by spin coating onto the top facing side of a fused silica substrates and annealed for 15\\u00a0min at 60\\u00a0\\u00b0C. The average film thickness was measured to be 300\\u00a0nm. Table\\u00a01 shows the values for the figures of merit (FOM) calculated for PMMA:KB films. The detailed definition of the parameters listed in Table\\u00a01 was given in a previous work .\\nThe calculations of the FOMs were based on absorbance and photoluminescence (PL) spectra of the PMMA:KB layer, and on the External Quantum Efficiency (EQE) curve of the perovskite-based device, as shown in Fig.\\u00a01 . PL was measured with a Horiba Scientific Fluoromax 4 spectrofluorometer, with excitation at 375\\u00a0nm (at the maximum of optical absorption of the layer). EQE spectra were recorded using a Bentham TMC300 monochromator, with measurements taken every 1\\u00a0nm using a Stanford Research System SR830 lock-in amplifier. As seen in Fig.\\u00a01, the optical absorption of the PMMA:KB layer is between 350 and 420\\u00a0nm, so this should prevent any UV light in this region entering the absorber layer.\\nFor control, a UV filter was supplied from Solaronix (Switzerland), which cuts off light with wavelengths less than 390\\u00a0nm.\\n\\nMethylammonium Iodide (MAI, code 14965-49-2) and Lead (II) Chloride (PbCl2, code 7758-95-4) were purchased from Lumtec (Taiwan) with 99.999% purity. Dimethyl sulphoxide (DMSO, code 67-68-5) and Isopropyl alcohol (IPA, code 67-63-0) were purchased from Sigma-Aldrich (UK). Anisole (#495 A8) was supplied by MicroChem. All products were used as received.\\nFor photo-degradation studies, glass substrates were cleaned in ultrasound bath by immersion for 5\\u00a0min in deionised water, acetone and finally IPA. Lastly the substrates were dried under nitrogen flux and oxygen-plasma treated for 5\\u00a0min. Methylammonium iodide (MAI) solution was prepared by dissolving the solid in IPA with proportion of 30\\u00a0mg/ml, and stirred for 15\\u00a0min in ambient temperature. PbCl2 was dissolved into DMSO at a concentration of 300\\u00a0mg/ml and stirred at 70\\u00a0\\u00b0C for 20\\u00a0min. The absorber deposition was undertaken in a glove box (with water and oxygen concentrations below 0.1\\u00a0ppm) using the two-step sequential deposition method. The PbCl2 solution was spin-coated at 6000\\u00a0rpm and dried for 20\\u00a0min\\u00a0at 90\\u00a0\\u00b0C. After drying the substrates were left to cool down to room temperature before the next layer was deposited. A solution of MAI was then spin-coated at 6000\\u00a0rpm, after which the samples were again placed on a hotplate set to 90\\u00a0\\u00b0C and annealed for 20\\u00a0min.\\nThe devices analysed in this work were manufactured onto indium-tin oxide (ITO) coated glass substrates which were coated with a layer of PEDOT:PSS (AI4083). Subsequently, the absorber was deposited inside a glove box by spin-coating using the two-step procedure described above. The acceptor was 6,6-phenyl-C71-butyric acid methyl ester (PC71BM) dissolved in chlorobenzene (30\\u00a0mg/ml). Finally, thermal evaporation of 100\\u00a0nm of silver (Ag) was deposited to form the cathode of the device.\\n\\nAll measurements were undertaken in an air-conditioned room with relative humidity of 35\\u00a0\\u00b1\\u00a05% and ambient temperature of 20\\u00a0\\u00b1\\u00a05\\u00a0\\u00b0C. For photo-degradation studies, samples were kept at a constant temperature of 60\\u00a0\\u00b0C whilst simultaneously exposing to a Solar Simulator with an output power of 100\\u00a0mW/cm2 and AM 1.5G spectrum (calibrated using a silicon reference cell from RERA, Netherlands). Absorbance measurements were taken every 10\\u00a0min.\\nThe PSC current density-voltage (J-V) curves were measured for six devices illuminated by the same solar simulator. For this work, three configurations were used whereby the light facing side of the device was covered with a UV filter, PMMA:KB LDS layer or without filtration. For stability tests, the devices were constantly light soaked illumination interrupted for the J-V measurements made every 5\\u00a0min. The test corresponded to the ISOS-L-2 protocol .\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-70,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 90,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 20.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 60.0; 60.0,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: 30,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 0,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Hydroiodic acid (45&#x202F;wt.% in water), methylamine (30% in methanol), lead iodide (PbI2), acetic acid (99%), stannic chloride (SnCl4), tetrabutyl titanate, N,N-dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF), isopropyl alcohol, methanol, ether, chlorobenzene, acetonitrile, and Triton X-100 were purchased from Shanghai Chemical Agent Ltd., China (Analysis purity grade). Lithium bis(trifluoromethylsulphonyl) imide (Li-TFSI) and 4-tert-butyl-pyridine (TBP) were purchased from Aldrich. Spiro-OMeTAD was purchased from Shenzhen Feiming Science and Technology Co., Ltd. The above agents were used without further purification. F-doped tin oxide (FTO) glass substrates were purchased from NSG, Japan (15&#x202F;\\u03a9 sq\\u22121).\\nMAAc was prepared by reacting 15&#x202F;mL of methylamine and 5&#x202F;mL of acetic acid with 60&#x202F;mL of ethanol as solvent in a 250&#x202F;mL round-bottom flask at room temperature for 2&#x202F;h with stirring. Then the resulting solution was evaporated at 50&#x202F;\\u00b0C overnight, finally producing a light yellow liquid.\\nMAI was synthesized by reacting 20&#x202F;mL hydroiodic acid and 20&#x202F;mL methylamine in a 250&#x202F;mL round-bottomed flask at 0&#x202F;\\u00b0C for 2&#x202F;h with stirring. The solvent as well as excess reactant was removed by vacuum at 50&#x202F;\\u00b0C for 1&#x202F;h. Then the product was washed with diethyl ether and dried at 60&#x202F;\\u00b0C vacuum overnight.\\n\\nSnO2 compact layer was spin-coated onto the etched FTO substrate (2.0&#x202F;cm&#x202F;\\u00d7&#x202F;2.0&#x202F;cm) with a mixed solution of 0.10&#x202F;mol&#x202F;L\\u22121 SnCl4 and 4.00&#x202F;\\u03bcL&#x202F;mL\\u22121 triton X-100 in isopropyl alcohol at 500&#x202F;r.p.m. for 10&#x202F;s then at 2500&#x202F;r.p.m. for 20&#x202F;s, then annealed on a hotplate in air at 135&#x202F;\\u00b0C for 15&#x202F;min []. TiO2 electron-transporting layer (ETL) was prepared by spin-coating the TiO2 slurry onto the SnO2 compact layer with a spin rate of 500&#x202F;r.p.m. for 10&#x202F;s then at 2500&#x202F;r.p.m. for 30&#x202F;s, and then heat-treating at 450&#x202F;\\u00b0C for 30&#x202F;min [].1.10&#x202F;mol&#x202F;L\\u22121 PbI2 precursor solution without or with 9% MAAc (molar ratio) in a mixed solvent of DMF and DMSO with a volume ratio of 7: 3 was first step spin-coated on the aforementioned TiO2 ETLs at 2500&#x202F;r.p.m. for 30&#x202F;s and rinsed with chlorobenzene, then the products were annealed on a hotplate at 100&#x202F;\\u00b0C for 20&#x202F;min in air to achieve the PbI2 or PbI2&MAPbI3-x(Ac)x films. After drying, a solution of MAI in isopropyl alcohol (10&#x202F;mg&#x202F;mL\\u22121) was second step spin-coated onto the PbI2 or PbI2&MAPbI3-x(Ac)x films at 2500&#x202F;r.p.m. for 30&#x202F;s and rinsed with isopropyl alcohol, then the obtained products were heat-treated on the hotplate at 100&#x202F;\\u00b0C for 10&#x202F;min in air to fabricate the MAPbI3 or MAPbI3-x(Ac)x films.\\nA hole-transporting layer (HTL) of spiro-OMeTAD was deposited on the above-mentioned PbI2, MAPbI3, PbI2&MAPbI3-x(Ac)x, and MAPbI3-x(Ac)x films, respectively, by spin-coating at 2500&#x202F;r.p.m. for 20&#x202F;s in air, then annealing on a hotplate at 60&#x202F;\\u00b0C for 15&#x202F;min in air. The obtained devices were named as PSC-a, PSC-b, PSC-c, and PSC-d, respectively. The spiro-OMeTAD solution was prepared by dissolving the spiro-OMeTAD in chlorobenzene at a concentration of 65&#x202F;mM, with the addition of 200&#x202F;mM of TBP and 30&#x202F;mM Li-TFSI from a stock solution in acetonitrile.\\nFinally, 100&#x202F;nm of gold was thermally evaporated onto the HTL under high vacuum (<3&#x202F;\\u00d7&#x202F;10\\u22124&#x202F;Pa) by using a thermal evaportation system (ZHD400, Beijing Technol Science Co., Ltd. China) with a shadow mask to pattern the electrodes.\\n\\nThe phase identification of the samples was conducted with powder X-ray diffraction (XRD, BRUKER D8-ADVANCE). The surface morphology and the cross-sectional images of the samples were observed using a Field Emission Scanning Electron Microscope (FESEM, JEOL-JSM-6701F) operating at 10&#x202F;kV. Ultraviolet to visible (UV-Vis) absorption spectra of the samples were performed with an Agilent 8453 UV-Vis diode array spectrophotometer. The electrochemical impedance spectroscopy (EIS) of the PSC was carried out using a Zennium electrochemical workstation (Zahner) under the irradiation condition with an incident light intensity of 100&#x202F;mW&#x202F;cm\\u22122 (AM 1.5) by a solar simulator, and the impedance data covered a frequency range of 1\\u2013105&#x202F;Hz with 5&#x202F;mV of amplitude and 0&#x202F;V of bias potential. The resultant impedance spectra were fitted using Z-view software. The incident monochromatic photon-to-current conversion efficiency (IPCE) curves of PSC were performed with a Zennium CIMPS-pcs2 (Zahner) system by the tunable light source (TLS03). The photocurrent density-voltage (J-V) characteristic of the PSC was carried out using a computer-controlled CHI660D in ambient atmosphere. The incident light intensity was set under 100&#x202F;mW&#x202F;cm\\u22122 (AM 1.5&#x202F;G).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: MAAc,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The vacuum system used to prepare perovskite films was a dual-source thermal evaporator. The setup is schematically shown in Fig. S1. To obtain the accurate deposition rate of MAI, the deposition rate of MAI can be quantified by the partial pressure of MAI [,,]. Several batches of perovskite films were prepared with a varied MAI partial pressure (0.8\\u202f\\u00d7\\u202f10\\u22125 to1.4\\u202f\\u00d7\\u202f10\\u22125\\u202fTorr) and a fixed PbI2 rate (0.4\\u202f\\u202f\\u00c5\\u202fs\\u22121) to find out the optimal perovskite deposition condition. According to the X-ray diffraction (XRD) results, the optimal perovskite deposition condition was a MAI partial pressure of 1.2\\u202f\\u00d7\\u202f10\\u22125\\u202fTorr and a PbI2 rate of 0.4\\u202f\\u202f\\u00c5\\u202fs\\u22121 [].\\n\\nPSC devices were fabricated on fluorine-doped tin oxide (FTO) coated glasses (DSG, DHS-FTO22). Substrate preparation is the same as reported previously []. A 20\\u202fnm thick TiO2 compact layer was deposited on the FTO substrate at 2500 r.p.m for 60\\u202fs by spin-coating a mildly acidic solution of titanium isopropoxide (Sigma, 97%) in ethanol, and annealed in a muffle furnace at 500\\u202f\\u00b0C for 30\\u202fmin in air. Afterwards, the TiO2 coated substrate was transferred into a N2-filled glove box, where the PCBM layer was spin-coated from a PCBM precursor solution (10% in chlorobenzene) at 3000 r.p.m for 60\\u202fs and subsequently dried at 100\\u202f\\u00b0C for 10\\u202fmin. Three approaches were used to fabricate MAPbI3 perovskite films, as shown in Fig. 1 . Common co-evaporation was taken as a reference method, in which the perovskite films were simply deposited under the optimal growth condition. On the PCBM coated substrates, a 260\\u202fnm thick perovskite layer was deposited for device A0. For devices A5, A10, A20, a PbI2 layer with a thickness of 5, 10, 20\\u202fnm, respectively, was deposited with a PbI2 deposition rate of 0.4\\u202f\\u00c5\\u202fs\\u22121 prior to the growth of perovskite films. In SVHM (device B), prior to vacuum deposition of perovskite films, a 80\\u202fnm thick perovskite layer was deposited in glove box by spin-coating from a homogeneous 10% wt.% CH3NH3PbIxCl3\\u2212x precursor solution at 6000 r.p.m for 60\\u202fs and followed by annealing at 100\\u202f\\u00b0C for 70\\u202fmin. To form the precursor solution, methylammonium iodide and lead (II) chloride (99%, Sigma-Aldrich) were dissolved in anhydrous N,N-Dimethylformamide (DMF) (Sigma-Aldrich) at a 3:1\\u202fM ratio of MAI to PbCl2, with final concentrations 0.22\\u202fM lead chloride and 0.66\\u202fM methylammonium iodide. In SAFVM (device C), a 20\\u202fnm thick PbI2 layer was firstly deposited with a rate of 0.4\\u202f\\u00c5\\u202fs and then exposed to MAI vapor with MAI partial pressure of 1.2\\u202f\\u00d7\\u202f10\\u22125\\u202fTorr to convert the PbI2 film to perovskite film. After exposing to MAI atmosphere for certain times, perovskite films were deposited under optimal growth condition. After the deposition of perovskite films, a hole transport layer (HTL) was spin-coated at 3000 r.p.m for 60\\u202fs in glovebox. The composition of HTL was 0.170\\u202fM 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9\\u2032-spirobifluorene (spiro-OMeTAD, Merck), 0.064\\u202fM bis (trifluoromethane) sulfonimide lithium salt (LiTFSI, 99.95%, Aldrich) and 0.198\\u202fM 4-tert-butylpyridine (TBP, 96%, Aldrich) in the mixed solvent of chlorobenzene (99.8%, Aldrich) and acetonitrile (99.8%, Aldrich) (chlorobenzene:acetonitrile\\u202f=\\u202f1:0.1 v/v). Finally, 80\\u202fnm gold electrodes with active area of 0.1\\u202fcm2 were thermally evaporated on top of the devices to form the back contact under a vacuum of 10\\u22125\\u202fTorr.\\n\\nAfter the deposition of perovskite films, the samples were taken out of the load-lock chamber into a N2-filled glovebox. A part of the samples were then measured by XRD immediately within 10\\u202fmin to evaluate the crystalline structure. The samples used for scanning electron microscopy (SEM) measurements were protected in a home-made N2-filled box for the least exposure to air to ensure that the samples did not deteriorate before the measurements. The XRD measurement was taken on a Rigaku D MAX-3C (Cu-Ka, \\u03bb\\u202f=\\u202f1.54050\\u202f\\u00c5). The SEM measurement on the morphology of the perovskite films was taken on a JEOL JSM-6700F. The film thickness was obtained by means of a step profilometer (Surfcorder ET 150, Kosaka Lab Ltd).\\n\\nThe current density-voltage (J\\u2212V) curves were measured by a 2400 source meter from Keithley Instruments Inc. under simulated AM 1.5 sunlight at 100\\u202fmW\\u202fcm\\u22122 irradiance generated by a High Power Shutter Assembly for SS-1KW Solar Simulators (Sciencetech), with the intensity calibrated with an calibrated KG5 filtered Si reference cell. The J\\u2212V curves were obtained in air through reverse scan (1.1\\u202fV to \\u22120.2\\u202fV) with a step of 50\\u202fmV\\u202fat dwell time of 150\\u202fms. External quantum efficiency (EQE) was measured by an ORIEL IQE-200 instrument.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> none,\\n Perovskite_deposition_procedure: Spin-coating >> Evaporation,\\n Perovskite_deposition_thermal_annealing_temperature: 100.0 >> Unknown,\\n Perovskite_deposition_thermal_annealing_time: 70.0 >> Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fig. 1 shows the chemical structures of SAF and PEDOT:SAF. The dispersant SAF was prepared by one-pot reaction including sulfonation of formaldehyde and copolymerization between sulfonated bodies and acetone in alkaline condition. Formaldehyde, acetone and sodium sulphite were fed in a molar ratio of 2:1:1. 8.2\\u202fg of Na2SO3 solid was dissolved in 20\\u202fmL of deionized water at 45\\u202f\\u00b0C, keeping pH\\u202f=\\u202f10 with the addition of 20% NaOH. After adding 16\\u202fmL of formaldehyde (37%) and 8.0\\u202fmL of acetone rapidly, the mixture was heated up to 85\\u202f\\u00b0C and refluxed for 5\\u202fh. The brown crude product was in a process of vacuum rotary evaporation to drive out the residual reactants. The unpurified SAF seriflux with 14.5% solid content should be adjusted around pH\\u202f=\\u202f2 by adding 20% HCl before being used to prepare PEDOT:SAF.\\nThe SAF seriflux and 1.0\\u202fg of EDOT were dispersed in 50\\u202fmL deionized water according to the 1:1 mass ratio of EDOT and SAF. The solution was well mixed after 10\\u202fmin slow stirring, and its pH value could be adjusted to 2 by adding 20% HCl. Next, 1.9\\u202fg of APS used as oxidant was dissolved in water (5\\u202fmL) and added dropwise. The mixed solution was kept at room temperature under high stirring speed for 48\\u202fh, ensuring the complete reaction of the EDOT monomers. To avoid interference from impurities during the following characterization, the crude solution was purified by using a dialysis membrane (MWCO 1000\\u202fDa) for a week. The mass concentration of PEDOT:SAF should be concentrated above 1%, which can be calibrated by the peak of the UV absorption spectrum at 800\\u202fnm.\\n\\nPoly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS, Clevios PVP Al 4083 purchased from Heraeus Holding GmbH), Methylammonium iodide (MAI, 99.9% from Dyesol Ltd), Lead iodide (PbI2, 99.999%, Sigma), Lead chloride (PbCl2, 99.999%, Sigma), Dimethyl sulphoxide (DMSO, 99.8%, Sigma), \\u03b3-Butyrolactone (GBL, 99.8%, Aladdin), Toluene (99.8%, Sigma-Aldrich), isopropanol (IPA, 99.5%, Sigma-Aldrich), phenyl-C61-butyric acid methyl ester (PCBM, 98%, nano-c), Chlorobenzene (99.8%, Sigma), Bathocuproine (BCP) were used as received without further purification.\\n\\nThe devices were prepared with the typical structure of ITO/HTL/CH3NH3PbIxCl3-x(350\\u202fnm)/PCBM(55\\u202fnm)/BCP/Ag [,]. Two kinds of hole-transporting layer (HTLs) including PEDOT:PSS (\\u223c24\\u202fnm) and PEDOT:SAF (\\u223c27\\u202fnm) were applied as the HTLs, respectively. The planar PSCs were fabricated on pre-patterned ITO glass substrates (around 2\\u202f\\u00d7\\u202f2.5\\u202fcm2 in size, 10\\u202f\\u03a9 per square). The patterned ITO glass substrates were sequentially ultrasonic cleaned with detergent, deionized water, acetone, isopropyl alcohol for 20\\u202fmin, respectively. Then the ITO substrates were dried with nitrogen and treated with UV ozone for 30\\u202fmin before an HTL was spin-coated on the substrates at 6000\\u202frpm for 40\\u202fs and annealed at 125\\u202f\\u00b0C for 20\\u202fmin. After that, the substrates were transferred into a nitrogen-filled glovebox. The CH3NH3PbIxCl3-x precursor solution was prepared by mixing 1.26\\u202fM PbI2, 0.14\\u202fM PbCl2 and 1.35\\u202fM MAI dissolved in the co-solvent of DMSO:GBL (3:7 v/v), and stirred for 1\\u202fh\\u202fat 80\\u202f\\u00b0C. The solution was then spin-coated onto the hole-transporting layer with solvent engineering method. The spin coating process was programmed to run at 1000\\u202frpm for 20\\u202fs and then 4000\\u202frpm for 45\\u202fs. When the total spinning time was 50\\u202fs, 350\\u202f\\u03bcL anhydrous toluene was injected onto the substrates. The perovskite films were annealed on the hotplate at 100\\u202f\\u00b0C for 20\\u202fmin. To increase the crystallinity of perovskite film, 40\\u202f\\u03bcL IPA was added to give a solvent annealing process []. After that, a layer of phenyl-C61-butyric acid methyl ester (PCBM) (20\\u202fmg/mL in chlorobenzene) was spin-coated on the top of the perovskite layer at 2000\\u202frpm for 45\\u202fs. BCP interlayer (0.5\\u202fmg/mL in IPA, 5\\u202fnm) was coated after that, and then the devices were finished by thermally evaporated 100\\u202fnm Ag. All the devices had an area of 12.5\\u202fmm2. All current density\\u2012voltage (J\\u2012V) curves were tested under simulated AM 1.5G illumination at an intensity of 100\\u202fmW/cm2 with an XES-70S1 solar simulator and the data were recorded by a Keithley 2400 source meter unit. Before the test, the system was calibrated using an NREL-certified monocrystal Si photodiode detector. All of the measurements were carried out in air at room temperature without encapsulation. The morphologies and thicknesses of the thin layers were measured using atomic force microscopy (AFM) (Agilent 5500). Scanning electron microscopy (SEM) images were acquired by a JSM-7800\\u202fF SEM. The steady-state photoluminescence (PL) spectra were obtained on an Edinburgh Instruments FLS920 spectrofluorometer, and the excitation wavelength was 630\\u202fnm. Cyclic voltammetry (CV) was performed in CH2Cl2 solution with 0.1\\u202fM tetrabutylammoniun hexafluorophosphate (Bu4NPF6) as the supporting electrolyte on electrochemistry workstation (CHI660E, China). The UV\\u2013visible absorption spectra were recorded by a PerkinElmer Lambda 950 spectrophotometer. The X-ray diffraction (XRD) data of the perovskite films were collected by a Bruker D8 Advance XRD instrument.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Unknown,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 24,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1056,\\n Stability_PCE_initial_value: 15.8,\\n Stability_PCE_end_of_experiment: 81,\\n Cell_area_measured: ,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI, 99.8%), Formamidinium iodide (FAI, 99.8%), and Tris [2-(1H-pyrazol-1-yl)-4-tert-butylpyridine] cobalt (III) tris[bis (trifluorome-thylsulfonyl)imide] (FK209) were acquired from Dyesol Ltd., Queanbeyan, Australia. Lead iodide (PbI2, 99.999%), Lead chloride (PbCl2, 99.999%), Chlorobenzene (CB, 99.8%), N,N'-Dimethylformamide (DMF, 99.8%), isopropanol (IPA, 99.5%), titanium(IV) chloride (TiCl4, \\u2265 98.0% purity), acetonitrile (anhydrous, 99.8% purity), bis(trifluoromethane)sulfonimide lithium salt (Li-TFSI, 96% purity), and 4-tert-butylpyridine (TBP, 98% purity) were purchased from Sigma-Aldrich, Saint Louis, MI, USA. Phenyl-C61-butyric acid methyl ester (PC61BM, 98%) was acquired from Nano-C, Westwood, MA, USA. Spiro-OMeTAD (99.8%) was supplied by Xi\\u2019an Polymer Light Technology Corp. Stannic oxide (SnO2) nanoparticles precursor was purchased from Alfa Aesar. Unless stated otherwise, the materials were used as received without further purification.\\n\\nPlanar-type PSCs were fabricated on pre-patterned ITO/glass substrates (size: 2\\u202f\\u00d7\\u202f2.5\\u202fcm2, sheet resistivity: 10\\u202f\\u03a9/\\u25a1). The patterned ITO glass substrates were sequentially ultrasonic cleaned with detergent, de-ionized water, acetone, and alcohol at 50\\u202f\\u00b0C for 20\\u202fmin, respectively. They were dried with nitrogen and treated in a UV ozone oven for 15\\u202fmin. Followed by the formation of TiO2 layer. If ALD process is adopted, the deposition will be carried out using a commercial ALD system (Savannah S200, Cambridge Nanotech). High-purity Nitrogen (N2) was continuously introduced to the ALD chamber at a flow rate of 15 sccm to achieve a base pressure of \\u223c0.3\\u202fTorr. The sample chamber was kept at 150\\u202f\\u00b0C for all experiments. C8H24N4Ti precursor was hold at 120\\u202f\\u00b0C to achieve reasonable vapor pressure for deposition. Standard pulse times for C8H24N4Ti and H2O were 0.1\\u202fs, and 0.1\\u202fs, respectively, with purge times kept constant at 40\\u202fs. After 120 recycles, the TiO2 film can be obtained. After deposition, the thickness of TiO2 layer is about 10\\u202fnm. The fitted thickness of TiO2 layer by ellipsometer spectra is 9.24\\u202fnm (Fig. S1). If solution method is employed, the substrates would be immersed into 40\\u202fmM TiCl4 aqueous solution at 70\\u202f\\u00b0C for 60\\u202fmin. The TiCl4 treated ITO substrates are washed thoroughly with deionized water and blow-dried by nitrogen gas, and further annealed at a hot plate at 250\\u202f\\u00b0C in air for 30\\u202fmin to form the TiO2 layer. Then a SnO2 layer was formed on ITO/TiO2 substrates by spin-coating a diluted SnO2 nanoparticles precursor (the mass ratio of SnO2:H2O is 1:3) at 3000\\u202frpm for 30\\u202fs and annealed at 150\\u202f\\u00b0C for 30\\u202fmin. After that, the ITO/TiO2/SnO2 substrates were transferred into a nitrogen-filled glove box and spin-coated with a PC61BM solution (10\\u202fmg/mL in chlorobenzene) at 6000\\u202frpm for 45\\u202fs, followed by heating at 100\\u202f\\u00b0C for 5\\u202fmin. 1.36\\u202fM PbI2 and 0.24\\u202fM PbCl2 were dissolved in the solvent of DMF and stirred for 2\\u202fh at 72\\u202f\\u00b0C. 100\\u202fmg MAI:FAI (7:3 mass. ratio) were dissolved in the solvent of 1\\u202fmL IPA with 1.0\\u202fvol% DMF. After that, PbX2 precursor solution was spin coated on the top of the PC61BM covered substrates at 3000\\u202frpm for 45\\u202fs, and then the solution of MAI:FAI was spin-coated on top of the PbX2 at 3000\\u202frpm for 45\\u202fs. All of the films were thermally annealed on the hotplate at 100\\u202f\\u00b0C for 10\\u202fmin. This process is carried out under the IPA atmosphere. Next, the hole transport layer (HTL) was spin-coated on ITO/TiO2/SnO2/PC61BM/ MA0.7FA0.3PbI(3-x)Cl(x) substrates at 1000\\u202frpm for 10\\u202fs and 4000\\u202frpm for 45\\u202fs using the prepared HTL solutions. The HTL solution containing 90\\u202fmg Spiro-OMeTAD in 1\\u202fmL chlorobenzene, 45\\u202f\\u00b5L Li-TFSI/acetonitrile solution (170\\u202fmg/mL), 10\\u202f\\u00b5L tBP, and 75\\u202f\\u00b5L Co(III) complex FK209/acetonitrile solution (100\\u202fmg/mL). The devices were finished by thermally evaporated 100\\u202fnm Ag. All the devices have an active area of 0.07\\u202fcm2 defined by a shadow mask.\\n\\nThe morphologies of the perovskite films were characterized by the atomic force microscope (AFM) (Bruker Dimension Icon, Bruker, Karlsruhe, Germany) and extreme-resolution analytical field emission scanning electron microscope (SEM) (JSM-7800F, JEOL Ltd., Tokyo, Japan). The X-ray diffraction (XRD) patterns were obtained from an X-ray diffractormeter using Cu K\\u03b1 radiation source (D8 Advance, Bruker, Germany). The absorption spectra of perovskite samples were measured by an UV\\u2013visible spectrophotometer (Perkin-Elmer Lambda 950). The ellipsometer (WVASE 32, J. A. Woollam Co., Inc.) was used to fit the thickness of TiO2 film. The XPS (X-ray photoelectron spectroscopy) was carried out on an Escalab 250Xi using monochromatic Al K\\u03b1 (1486.6\\u202feV). The photovoltaic performances of PSCs were measured by using a Keithley 2400 source meter (Tektronix, Inc., Beaverton, OR, USA) under the simulated AM 1.5G (1 sun) illumination of 100\\u202fmW/cm2 from a sunlight simulator (XES-300T1, SEN-EI Electric. Co. Ltd, Osaka, Japan). The illumination intensity was calibrated by a reference silicon solar cell certificated by the National Renewable Energy Laboratory (NREL). The incident photo-to-current conversion efficiency (IPCE) was measured by the quantum efficiency measurement system (SCS10-X150, Zolix instrument. Co. Ltd, Beijing, China). Transient photocurrent (TPC) measurement was performed with a system excited by a 532\\u202fnm (1000\\u202fHz, 3.2\\u202fns) pulse laser. Transient photovoltage (TPV) measurement was performed with the same system excited by a 405\\u202fnm (50\\u202fHz, 20\\u202fms) pulse laser. A digital oscilloscope (Tektronix, D4105, Beaverton, OR, USA) was used to record the photocurrent or photovoltage decay process with a sampling resistor of 50\\u202f\\u03a9 or 1\\u202fM\\u03a9, respectively. EIS measurements were performed on an electrochemical workstation (CHI600E, Shanghai Chenhua) with a 10\\u202fmV amplitude perturbation and frequencies between 100\\u202fHz and 1\\u202fMHz. M-S plots were recorded on the same system under AC excitation amplitude of 30\\u202fmV at a frequency of 5\\u202fkHz. All the measurements were performed under ambient atmosphere at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c | SnO2-np | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: ALD | Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.3MA0.7PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Unknown,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The perovskite solar cells were fabricated on patterned ITO coated glass substrates with a sheet resistance of 15 \\u03a9/sq. The devices have a structure of ITO/CuI/PbPc/MAPbI3/C60/4,7-diphenyl-1,10-phenanthroline (Bphen)/Ag (as shown in Fig. 1), for reference, device with a PEDOT:PSS HTL was also fabricated. The ITO substrates were routinely cleaned followed by UV-ozone treatment for 15 min. Then they were transferred to a vacuum chamber, and 2 nm CuI and 20 or 50 nm PbPc were thermal evaporated in sequence at a pressure of 5\\u00d710\\u22124 Pa. For the reference device, PEDOT:PSS (Clevios P-VP Al4083) was firstly passed through a 0.45 \\u00b5m filter and deposited onto ITO substrate through spin-coating at 4000 rpm for 40 s, then the samples were dried at 120 \\u00b0C for 15 min, which forms a PEDOT:PSS layer of about 40 nm. PbI2 and CH3NH3I (MAI) were dissolved in DMF and IPA with concentrations of 460 and 50 mg/ml, respectively. PbI2 solution was heated at 100 \\u00b0C for about 10 min before using to make sure PbI2 can be fully dissolved. The dissolved PbI2 solution was spun on CuI/PbPc or PEDOT:PSS substrates at 2000 rpm for 30 s. Then they were transferred onto a hot plate quickly and dried at 100 \\u00b0C for 3 min to vapor the residual solvent. The MAI solution was spun on top of dried PbI2 films at 2000 rpm for 30 s at room temperature. The spin coated PbI2/MAI stacking films were annealed at 100 \\u00b0C to fully convert PbI2 to perovskite, and the optimized time was 40 min for the films on PbPc and 120 min for that on PEDOT:PSS. All the above fabrication procedures were performed in ambient atmosphere (humidity of about 50% and temperature of 28 \\u00b0C). Finally, the devices were completed by thermal evaporating 40 nm C60, 5 nm Bphen, and 100 nm Ag in sequence in a vacuum chamber at a pressure of 5\\u00d710\\u22124 Pa. Deposition rate and layer thickness were monitored in situ using oscillating quartz monitors. Evaporation rates were kept at 1 \\u00c5/s for CuI, PbPc, C60, and Bphen, and 10 \\u00c5/s for Ag cathode. The device area is 0.18 cm2, determined by the overlap of the cathode and anode electrodes.\\nX-ray diffraction (XRD) patterns were measured with a Rigaku D/Max-2500 diffractometer using Cu K\\u03b1 radiation (\\u03bb=1.54 \\u00c5). Absorption spectra were recorded on a Shimadzu UV-3101PC spectrophotometer. Scanning electron microscopy (SEM) images were measured by a Hitachi S4800 field emission scanning electron microscopy. The surface topographies were imaged with a Bruker MultiMode 8 at. force microscope (AFM) in tapping mode. The wettabilities were measured by a Sl-2800 optical contact angle measuring device (Shanghai Solon Information Technology Co., Ltd.). Current-voltage (J-V) characteristics of the devices were measured with a Keithley 2400 source meter both in dark and under illumination of a Xe lamp light source with an AM 1.5 G filter, and the irradiation intensity was certified to be of 100 mW/cm\\u22122. The voltage scans were swept from short circuit to forward bias with a rate of 0.05 V/s. The incident photon to current conversion efficiency (IPCE) spectra were performed with a Stanford SR803 lock-in amplifier under monochromatic illumination. All measurements were performed under ambient conditions.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | Bphen,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100 >> 100,\\n Perovskite_deposition_thermal_annealing_time: 3.0 >> 40.0,\\n HTL_stack_sequence: CuI | PbPc,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Evaporation | Evaporation,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 28.0; 28.0,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 1320,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 50,\\n Cell_area_measured: 0.18,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The following materials were purchased from commercial suppliers without further purification: PEDOT:PSS (Clevious P VP AI 4083) and N,N\\u2032-Bis-(1-naphthalenyl)-N,N\\u2032-bis-phenyl-(1,1\\u2032-biphenyl)-4,4\\u2032-diamine (NPB) were obtained from Xi'an Polymer Light Technology Corp. Lead iodide (PbI2) was purchased from TCI Chemicals. Methylammonium iodide (MAI) was purchased from Dyesol (Australia). Anhydrous N, N-dimethyl formamide (DMF) and Dimethyl sulfoxide (DMSO) were purchased from Aldrich (U.S.) [6,6].-phenyl-C61-butyric acid methyl ester (PC61BM, 99.5%) was purchased from Lumtec Co. (Taiwan). 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) (99.9%) was purchased from Wako Co. (Japan).\\n\\nFTO-coated glass was ultrasonically cleaned twice by detergent, water, ultrapure water, acetone and isopropanol for 15\\u00a0min. After drying at 150\\u00a0\\u00b0C, the FTO glass was ultraviolet ozone (UVO) treated for 15\\u00a0min and cooled down to room temperature. Then, PEDOT:PSS (~25\\u00a0nm) was deposited on FTO via spin coating in air at 3000\\u00a0rpm for 30\\u00a0s, followed by annealing at 150\\u00a0\\u00b0C for 15\\u00a0min. 50\\u00a0\\u03bcL NPB solution in chlorobenzene was dripped onto the rotating PEDOT:PSS substrate at 3000\\u00a0rpm for 30\\u00a0s in N2 atmosphere. The optimal thickness of NPB buffer layer is ~15\\u00a0nm measured by spectroscopic ellipsometry. The perovskite layer (~350\\u00a0nm) was prepared according to the following literature []. PC61BM solution (20\\u00a0mg\\u00a0mL\\u22121 in chlorobenzene) was spin-coated on the perovskite layer at N2 atmosphere at 2000\\u00a0rpm for 30\\u00a0s. A thin layer of BCP was prepared on PC61BM by continuously dropping 125\\u00a0\\u03bcL saturated BCP solution (isopropanol) on revolving substrate at 6000\\u00a0rpm, followed by annealing at 40\\u00a0\\u00b0C for 5\\u00a0min. The thickness of PC61BM/BCP is ~60\\u00a0nm. Finally, 70\\u00a0nm thick Ag electrode was deposited by thermal evaporation on the top of device under 3\\u00a0\\u00d7\\u00a010\\u22124\\u00a0Pa. The active area of solar cells was 0.09\\u00a0cm2. The flexible devices were fabricated on polyethylene terephthalate/ultrathin (8\\u00a0nm) gold (PETUG) substrates and the active area of solar cells was 0.1225\\u00a0cm2.\\n\\nThe current-voltage (J-V) characteristics were measured by the Keithley 2400 Source Measure Unit in N2 atmosphere, integrated with a solar simulator (Newport 94043A, USA) under the standard AM 1.5G condition (100\\u00a0mW\\u00a0cm\\u22122). A certified standard silicon cell provided by Newport Corporation PV Lab was used as reference and the certificate is shown in Fig. S1. UV-light stability was tested using an UV analyzer with 254\\u00a0nm and 365\\u00a0nm light sources. The power of light sources is 6\\u00a0W. Ultraviolet photoelectron spectroscopy (UPS) was tested by ESCALAB 250Xi UPS system (Thermo Fisher Scientific) with He I\\u03b1 (21.22\\u00a0eV) emission line. The transmission and absorption spectra were measured by Shimadzu UV-3600 ultraviolet\\u2013visible (UV\\u2013vis) spectrophotometer. PL measurement of NPB solution and a series of PEDOT:PSS/NPB films was carried out using a fluorescence spectrophotometer (Hitachi F-4600, Japan). Scanning electron microscope (SEM) images were obtained on a field emission scanning electron microscope (Hitachi SU8010, Japan). Transient photovoltage decay, light intensity-dependent V oc, and electrochemical impedance spectra (EIS) were recorded by a Zahner electrochemical workstation. EIS was measured in the frequency range of 0.1\\u2013106\\u00a0Hz with an amplitude of 10\\u00a0mV. The light intensity of transient photovoltage decay measurement is 1000\\u00a0W\\u00a0m\\u22122. The step of light intensity-dependent V oc measurement is 10\\u00a0W\\u00a0m\\u22122 from 0-1000\\u00a0W\\u00a0m\\u22122. X-ray diffraction (XRD) spectra were obtained on an X-ray diffract meter (Rigaku miniflex 600, Japan) at a scan rate of 5\\u00b0 min\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS | NPB,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: TRUE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: 25; 25,\\n Stability_atmosphere: Air,\\n Stability_time_total_exposure: 480,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: 70,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"BP crystals were obtained from Smart Elements GmbH, Austria. Formamidinium iodide (H2NCHNH2I; FAI), methylammonium iodide (CH3NH3I; MAI), methylammonium bromide (CH3NH3Br; MABr), PbI2 and PbBr2 were purchased from Dyesol. N,N-Dimethylformamide (DMF, 99.9%), dimethyl sulfoxide (DMSO, 99.9%), 4-tert-butylpyridine (4-TBP, 96%), lithium bistrifluoromethane sulfonimidate (LiTFSI, 99.9%), and chlorobenzene (99.5%) were obtained from Sigma-Aldrich. All chemicals were used as received without further purification.\\n\\nThe BP crystals were ground into powder and added into NMP solution. Then, the mixtures were ultrasonicated using an ultrasonic bath (400 W) at 20 \\u00b0C for 8 h. The obtained BP mixture was purified by centrifugation, with a rate of 5000 rpm for 30 min, to remove larger particles. Then, the residual BP dispersion was further turned into BPQDs by probe sonication for 4 h.\\n\\nPrior to film deposition, a designed pattern was etched onto the ITO/PEN substrate (Peccell) using Zn powder and 2 M HCl solution, then successively well cleaned with detergent, absolute ethanol and DI water. A subsequent 10 min O2 plasma treatment was conducted to increase wettability of the ITO surface. BPQD films were fabricated by spin-coating the freshly prepared BPQD IPA solution at 1500 rpm for 30 s in a N2-filled glove box. The thickness of BPQD films was controlled by repeating the spin-coating process a certain number of times (i.e. 0, 1, 3, 5, and 7). Between each coating, the as-prepared film was dried at 60 \\u00b0C for 5 min. The FA0.85MA0.15PbI2.5Br0.5 perovskite films were deposited on the newly coated BPQD film using a procedure according to the reported work. The as-deposited films were heated at 100 \\u00b0C for 60 min for crystallization. For comparison, perovskite films were also deposited on the bare ITO/PEN or compact TiO2-coated FTO/glass substrates under the same conditions. The high-temperature-sintered TiO2 compact layer was deposited according to our previous work. A hole-transporting material (HTM) solution comprised by 61 mM spiro-OMeTAD, 55 mM tert-butylpyridine (TBP) and 26 mM Li-TFSI salt in chlorobenzene was spin-coated on the perovskite layer at 4000 rpm for 30 s. Au films with thickness of 80 nm were thermally evaporated on the electrodes, which were previously stored in a desiccator overnight, as the top electrode. The active area of each PSC is 0.09 cm2.\\n\\nThe morphology and structure of BPQDs were characterized by scanning transmission electron microscope (STEM, JEOL JEM-2100F) operated at 200 kV. The morphology of both the BPQDs on Si plate and BPQD films on ITO/PEN was imaged by AFM (Veeco Dimension-Icon system) with a scanning ratio of 0.977 Hz. The micrographs of the BPQD and perovskite films were obtained using a field-emission scanning electron microscope (FESEM, ZEISS Merlin) operated at 5 kV. The optical absorption of BPQDs was studied by a UV-Vis spectrophotometer (Hitachi U-3010, Japan). Raman spectra were collected using a Horiba Jobin Yvon HR800 Raman microscopic system equipped with a 488 nm laser operating at 180 mW. The spot size of the excitation laser is \\u223c1 \\u03bcm. The PL measurements were conducted on a FLS920P Edinburgh Analytical Instrument apparatus with a 485 nm laser excitation source. Photocurrent density\\u2013voltage (J\\u2013V) curves were recorded using a Keithley 2400 source meter under one sun AM 1.5 G illumination (100 mW cm\\u22122) supplied by a solar simulator (Enlitech SS-F7-3A, 300 W). The light intensity was calibrated using a silicon reference cell (NREL) equipped with a power meter. The incident photon-to-electron conversion efficiency (IPCE) was tested using an IPCE system (Enlitech QE-R).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.5I2.5,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Chlorobenzene (99.9%), N,N-dimethylformamide (DMF, 99.9%), titanium isopropoxide (99.999%), and acetonitrile (99.9%) were obtained from Sigma-Aldrich. Cerium(III) nitrate hexahydrate and isopropanol were obtained from Aldrich. 2,2\\u2032,7,7\\u2032-Tetrakis(N,N\\u2032-di-p-methoxyphenylamino)-9,9\\u2032-spirobifluorene (spiro-OMeTAD, 99.5%), PbI2 (99.99%), lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI, 99.9%), CH3NH3I (99.5%), and 4-tert-butylpyridine (tBP, 96%) were obtained from Xi'an Polymer Light Technology Company. Glass substrates coated with fluorine-doped tin oxide (FTO) (15 \\u03a9 sq\\u22121) were bought from OPV Tech New Energy Co. All the materials and reagents were used without further purification.\\n\\nThe FTO substrates were ultrasonically cleaned with an abstergent, acetone, deionized water, and ethanol for 15 min in each case. The conductive substrates were dried with a nitrogen gun and post-treated with UV\\u2013ozone for 15 min. A c-TiO2 layer was coated on the cleaned FTO substrates by spin coating with the titanium precursor solution at 2000 rpm for 30 s. The as-prepared c-TiO2 was post-annealed at 150 \\u00b0C for 15 min and then heated at 500 \\u00b0C for 30 min in a muffle furnace. Then, we started to prepare the mesoporous TiO2 precursor solution, and 15 mL hydrochloric acid was mixed with 15 mL deionized water under magnetic stirring for 10 min. Then, 0.75 mL tetra-n-butyl titanate with or without different amounts of cerium(III) nitrate pentahydrate (Ce(NO3)3\\u00b75H2O) as a dopant was added to the abovementioned mixed solution, and then the solution was vigorously stirred for 30 min to obtain a clarified solution. Afterwards, the clear solution was transferred into a reaction kettle equipped with compact TiO2/FTO substrates. The sealed reaction kettle was placed in a laboratory oven at 170 \\u00b0C for 1 h. After the autoclave was cooled to room temperature naturally, the substrate was taken out, rinsed with deionized water and ethanol twice to remove residual reactants, and finally dried with a nitrogen gun and then annealed at 500 \\u00b0C for 30 min in a muffle furnace. An MAPbI3 layer was spin-coated on c-TiO2/m-TiO2/FTO glass at 3000 rpm for 55 s. CB (80 \\u03bcL) was washed onto the substrate during the spin-coating method about 10 s before the beginning of the procedure, and the substrate was then annealed at 100 \\u00b0C for 20 min. An HTL film was manufactured by spin-coating a spiro-OMeTAD solution on a perovskite film at 3000 rpm for 30 s. Finally, an Ag electrode was deposited onto the spiro-OMeTAD layer by a sputtering technique to finish the manufacture of the cell.\\n\\nThe current\\u2013voltage characteristics of perovskite solar cells were determined using an electrochemical workstation under AM 1.5 simulated solar illumination (CEL-S500, Beijing, China). Mott\\u2013Schottky plots were recorded by employing an electrochemical workstation with a standard three-electrode configuration with Ag/AgCl as the reference electrode in saturated Na2SO4 and a Pt sheet as the counter electrode in deionized water. The morphology and composition of mesoporous TiO2 films were investigated using a scanning electron microscope (SEM; Zeiss EVOMA15) equipped with an energy-dispersive X-ray spectroscopy (EDX) detector. X-ray diffraction (XRD, DX-2700, Dandong) patterns were recorded from 22\\u00b0 to 58\\u00b0 with Cu K\\u03b1 radiation (\\u03bb = 0.15406 nm) at a scanning rate of 4\\u00b0 min\\u22121. X-ray photoelectron spectroscopy (XPS) measurements were carried out with an X-ray photoelectron spectrometer (Kratos Axis Ultra DLD) with a monochromated Al K\\u03b1 X-ray source (h\\u03bd = 1486.6 eV, 200 W). HRTEM images were recorded with a Hitachi HT-7700 transmission electron microscope (Hitachi Limited, Tokyo, Japan) at a voltage of 100 kV. UV-vis absorption spectra were recorded by a UV-vis spectrometer (Varian Cary 5000). Time-resolved photoluminescence (TRPL) spectra were recorded at 765 nm with an Edinburgh Instruments FLS 980 spectrometer with a pulsed diode laser at 485 nm (with an intensity of 0.12 mW cm\\u22122) at a pulse frequency of 1 MHz. Incident photocurrent conversion efficiency (IPCE) spectra were recorded using an IPCE system (PVE 300, Bentham, Inc.) as a function of the wavelength from 300 to 800 nm. The active area of the perovskite solar cells was fixed at 0.16 cm2 using a mask.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2), methylammonium (CH3NH3I) and chemicals needed to prepare spiro-OMeTAD solution were purchased from Xi'an Polymer Light Technology Corp (China). N,N-Dimethylformamide (DMF) was purchased from Sinopharm Chemical Reagent Co., Ltd (China). The transparent fluorine-doped tin oxide (FTO) conductive glasses with a sheet resistance of 15 \\u03a9 sq\\u22121 patterned using a laser were directly purchased from Weihua Solar Company (Xiamen, China).\\n\\nFTO glass substrates were washed by ultrasonication with acetone, ethanol, and deionized water for 15 min respectively. The TiO2 blocking layer of about 60 nm was spin-coated on the FTO substrate at 2000 rpm for 30 s using 0.15 M titanium diisopropoxide bis(acetylacetonate) (75 wt% in isopropanol, Aldrich) in 1-butanol (99.8%, Aldrich) solution followed by heating at 125 \\u00b0C for 10 min. After the TiO2/FTO substrate was treated at 450 \\u00b0C for 30 min, a 40 wt% perovskite precursor solution containing PbI2 mixed with CH3NH3I and HC(NH2)2I in the molar ratio of 1:0.9:0.1 in N,N-dimethylformamide (DMF) was spin-coated on the TiO2 blocking layer at 2500 rpm for 10 s. Then, the substrate was placed in a sample chamber connected to a gas pump system. It took about 4 s to transfer the substrate into the chamber. The gas pump system was home-made, and composed of a low pressure system with a larger vacuum buffer tank connected to the sample chamber by a gas drainage pipe controlled by a valve. At the bottom, the sample chamber was connected to two symmetrical gas tubes further connected to a gas flow controller respectively, which allows a certain amount of gas to flow to the surface of the wet perovskite film. And then opening the valve connecting the specimen chamber and the low pressure system, DMF solvent evaporates rapidly. After 5 s, closing the valve, and taking out the sample, a brown, somewhat transparent, FA0.1MA0.9PbI3 film with a mirror-like surface was obtained. The whole process took about 19 s from spin-coating to taking out the substrate. The sample chamber is very small with a volume of 0.04 L and the vacuum buffer tank is 108 L. The film was annealed at 120 \\u00b0C on a hot plate for 20 min, and then transferred into a glovebox containing <0.1 ppm of O2 and H2O. And then the spiro-OMeTAD solution (80 mg of spiro-OMeTAD, 28.5 \\u03bcL of 4-tert-butylpyridine, and 17.5 \\u03bcL of lithium-bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg Li-TFSI) in 1 mL acetonitrile) all dissolved in 1 mL of chlorobenzene was spin-coated onto the perovskite film by spin-coating at 4000 rpm for 30 s. The spiro-OMeTAD-coated substrates were stored in an auto-drying cabinet at 20 \\u00b0C with a relative humidity of 15% for at least 8 h. Finally, a 100 nm thick gold layer was deposited onto the spiro-OMeTAD layer by thermal evaporation. The perovskite films were completed in air with a temperature of 23 \\u00b0C and a relative humidity of 45\\u201360%.\\n\\nA field-emission scanning electron microscope (FSEM, TESCAN) was used to characterize the surface and fracture morphologies of the perovskite films. Atomic force microscopy (AFM, Innova) was used to characterize the surface roughness of the perovskite films. The steady-state photoluminescence spectra were measured using a compact steady-state spectrophotometer (Fluoromax-4, Horiba Jobin Yvon) with an excitation wavelength of 532 nm. A U-3010 spectrophotometer was used to measure the absorption spectra of the perovskite films. Photocurrent\\u2013voltage (J\\u2013V) characteristics of the devices were measured by using a source meter (2400, Keithley) under 100 mW cm\\u22122 illumination with a 450 W Class AAA solar simulator equipped with an AM 1.5G filter (Sol3A, Oriel). A standard Si reference cell (91150V, Oriel) was used to calibrate the exact light intensity of the solar simulator. The devices were measured by reverse (1.2 to \\u22120.2 V) and forward (\\u22120.2 to 1.2 V) voltage scanning at a scan step of about 23.7 mV (60 points in total) and a delay time of 1000 ms. The monochromatic incident photon-to-electron conversion efficiency (IPCE) was measured using a solar cell spectral response/QE/IPCE test system (QTest Station 500AD, CROWNTECH) in ac mode. The electrochemical properties of the perovskite solar cell were investigated by using electrochemical impedance spectroscopy, by using an electrochemical system (EIS, Zennium IM6, Zahner). A series of EIS spectra of the devices were measured at a bias voltage from \\u22120.1 V to \\u22121.0 V with a scan step of 0.1 V and at a frequency ranging from 3 MHz to 100 mHz with an ac amplitude of 20 mV under 10 W LED light.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.1MA0.9PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A 40 nm-thick layer of a TiO2 nanoparticle in ethanol with the appropriate amount of TiAcAc was spin-coated onto an ITO glass substrate and annealed at 150 \\u00b0C for 30 min. Next, the substrates were transferred into a nitrogen-filled glove box. A solution of CH3NH3PbI3\\u2212XClX in DMF was then spin coated onto the ITO/TiO2 substrate by spin-coating at 2000 rpm for 30 s. For the CH3NH3PbI3\\u2212XClX perovskite layer, the CH3NH3I powder was mixed with PbCl2 at a 3:1 mol ratio in DMF at 60 \\u00b0C for 12 h. Specifically, the concentration of the PbCl2 and CH3NH3I was 0.7 and 2.1 M, respectively. The films were then dried on a hot plate at 95 \\u00b0C for 90 min in air. The dopant-free DOR3T-TBDT HTL was spin-coated onto the perovskite layer. Here the concentration of DOR3T-TBDT is 18 mg mL\\u22121 in chloroform and the film thickness is \\u223c60 nm. The doped DOR3T-TBDT/chloroform (18 mg mL\\u22121, 0.4 mL) solution was prepared with the addition of 3 \\u03bcL Li-TFSI/acetonitrile (260 mg mL\\u22121), and 5 \\u03bcL tert-butylpyridine (tBP). The doped or dopant-free spiro-OMeTAD HTL was coated by spin coating (2000 r.p.m. for 30 s) 25 \\u03bcL of chlorobenzene solution. The spiro-OMeTAD without the dopant has the concentration of 160 mg mL\\u22121. For a doped solution, a spiro-OMeTAD/chlorobenzene (160 mg/1 mL) solution was employed with the addition of 35 \\u03bcL Li-TFSI/acetonitrile (260 mg mL\\u22121), and 28 \\u03bcL 4-tert-Butylpyridine. Finally, a 15 nm MoO3 layer and a 150 nm Ag layer were deposited in sequence on the HTL through shadow masks via thermal evaporation under high vacuum (\\u223c2 \\u00d7 10\\u22126 Torr). The effective area was 0.1 cm2. The current density\\u2013voltage (J\\u2013V) characteristics of photovoltaic devices were obtained using a Keithley 2400 source-measure unit. The photocurrent was measured under AM 1.5 G illumination at 100 mW cm\\u22122 under a Newport Thermal Oriel 91192 1000 W solar simulator. Unless stated otherwise, the devices were masked and measured under the reverse voltage scan with a scan rate of 1 V s\\u22121. The light intensity was calibrated using a KG-5 Si diode. External quantum efficiencies were measured by an Enli Technology (Taiwan) EQE measurement system. The effective area of each cell was 0.1 cm2 defined by masks for all the photovoltaic devices discussed in this work.\\n\\nA white light bias was generated from an array of diodes (Molex 180081-4320) to simulate 1 sun working conditions. A pulsed red dye laser (Rhodamine 6G, 590 nm) pumped using a nitrogen laser (LSI VSL-337ND-S) was used as the perturbation source, with a pulse width of 4 ns and a repetition frequency of 10 Hz. The perturbation light intensity was attenuated to keep the amplitude of transient \\u0394V below 5 mV. The current dynamics were recorded on a digital oscilloscope (Tektronix DPO 4104B), and the currents under short circuit conditions were measured over a 50 \\u03a9 resistor.\\n\\nThe complex impedance of the devices was recorded over the frequency range of 100 Hz to 1 MHz at room temperature under 1 sun, using the Z-\\u03b8 mode of a HP 4284A LCR precision meter. An AC drive bias of 30 mV and different DC voltages range from 0 to 0.9 V with a step of 0.1 V was employed. The EIS Spectrum Analyzer was used for the fitting of the impedance spectra.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 95,\\n Perovskite_deposition_thermal_annealing_time: 90,\\n HTL_stack_sequence: Spiro-MeOTAD | MoO3,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating | Evaporation,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"ITO-coated glass substrates were purchased from Shenzhen Nan Bo Group, China, with a sheet resistance of 10 \\u03a9 sq\\u22121. PbAc2\\u00b73H2O (99.998%, Aladdin), PbCl2 (99.999%, Alfa Aesar), lithium bis(trifluoromethylsulfonyl) imide (Li-TFSI) (99%, Aladdin), 4-tert-butylpyridine (t-BP) (97%, Adamas Reagent), DMF (Sigma-Aldrich, 99.8%), and chlorobenzene (99.9%, Alfa Aesar). Ethanol, isopropanol, acetone and acetonitrile were all purchased from Sinopharm Chemical Reagent Co., Ltd. 2,2\\u2032,7,7\\u2032-Tetrakis (N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (spiro-OMeTAD) was purchased from 1 M company. CH3NH3I was bought from Xi'an Polymer Light Technology Corporation. C60 was purchased from Suzhou Dade Carbon Nanotechnology Co, Ltd. 2-Pyridaldehyde and phenylhydrazine were purchased from TCI Co, Ltd. All reactants and solvents were used as received without further purification.\\n\\n1H and 13C NMR spectra were recorded on a Bruker AV 400 MHz NMR spectrometer. Tetramethylsilane (TMS) was used as the internal standard. Mass spectra were collected on a Bruker Autoflex Speed mass spectrometer. Electrochemical cyclic voltammetry was conducted on a CHI630D Electrochemical Workstation. A Pt disk was taken as the working electrode, Pt wire as the counter electrode, and saturated calomel electrode as the reference electrode. A solution of o-dichlorobenzene with 0.1 M tetrabutylammonium perchlorate (TBPA) was used as the electrolyte, and the scan rate was 50 mV s\\u22121. UV-Vis spectroscopy was performed on a UV-vis-NIR 3600 spectrometer (Shimadzu, Japan). Black single crystals of C60-PyP suitable for single-crystal X-ray diffraction were prepared by slowly diffusing n-hexane into a benzene solution of C60-PyP at 273 K for 3 weeks. Crystal data of C60-PyP were collected on a four-circle diffractometer (XtaLAB Synergy, Dualflex, HyPix) at 213 K. W scans were used for absorption corrections. The structure was solved with the direct method and refinement with SHELXL-2013.\\n\\nThe compound as (E)-2-((2-phenylhydrazono)methyl)pyridine (1 g, 5.08 mmol) was dissolved in acetonitrile solution (15 mL). Then N-chlorosuccinimide (1.49 g, 11.17 mmol) was added into the acetonitrile solution. The mixture solution was stirred with a magneton and slowly heated up to 80 \\u00b0C. The chlorination reaction progress was monitored using the TLC method. Finally, the solvent in the mixture solution was removed and the residual solid was purified with silica gel column chromatography. The resultant product is 0.43 g with the yield of 31.9%. 1H NMR (400 MHz, acetone) \\u03b4 9.54 (s, 1H), 8.62 (ddd, J = 4.9, 1.5, 1.0 Hz, 1H), 8.15 (d, J = 8.1 Hz, 1H), 7.87 (td, J = 7.8, 1.8 Hz, 1H), 7.46\\u20137.37 (m, 3H), 7.36\\u20137.29 (m, 2H). 13C NMR (101 MHz, acetone) \\u03b4 151.32, 149.07, 142.84, 136.43, 129.06, 125.50, 125.35, 123.68, 120.93, 115.21.\\n\\nTo a solution of C60 (144.0 mg, 0.2 mmol) in chlorobenzene (25.0 mL), N-(4-chlorophenyl)picolinohydrazonoyl chloride (36.0 mg, 0.4 mmol) and a few drops of triethylamine were added. Then, the mixture was heated at 80 \\u00b0C under a nitrogen atmosphere for 5 h and monitored with TLC. After cooling to room temperature, the solution was removed under reduced pressure. The crude product was purified by silica gel column chromatography, affording 49.7 mg of C60-PyP (yield of 34.5%). 1H NMR (400 MHz, CS2/D-acetone, ppm) \\u03b4 8.52 (s, 1H), 8.45 (d, J = 8.0 Hz, 1H), 7.94 (d, J = 7.5 Hz, 2H), 7.90 (s, 1H), 7.41 (d, J = 7.3 Hz, 2H), 7.32 (s, 1H). 13C NMR (101 MHz, CS2/D-acetone, ppm): \\u03b4 151.76, 149.10, 148.74, 147.59, 147.10, 146.96, 146.49, 146.40, 146.03, 146.00, 145.49, 145.25, 145.02, 144.66, 144.19, 143.12, 142.99, 142.90, 142.40, 142.34, 142.29, 142.23, 141.93, 141.88, 139.79, 139.30, 136.83, 136.59, 135.64, 130.79, 129.49, 124.94, 123.36, 123.31. MALDI-TOF m/z: calculated for C72H8N3Cl [M]\\u2212 949.68; found 949.4.\\nCrystal data for C60-PyP. Black blocks, 0.123 \\u00d7 0.098 \\u00d7 0.067 mm, monoclinic, space group P21/c, a = 19.9107(3) \\u00c5, b = 10.2319(2) \\u00c5, c = 20.5996(3) \\u00c5, V = 4195.74(12) \\u00c53, Fw = 2080, \\u03bb = 1.54184 \\u00c5, Z = 4, Dcalc = 1.628 Mg m\\u22123, \\u03bc = 1.314 mm\\u22121, T = 213 K; 25558 reflections, 7454 unique reflections; 5893 with I > 2\\u03c3(I); R1 = 0.0511 [I > 2\\u03c3(I)], wR2 = 0.1378 (all data), GOF (on F2) = 1.050. The maximum residual electron density is 0.311 e \\u00c5\\u22123. CCDC no. 1879301 contains the crystallographic data for C60-PyP.\\u2020\\n\\nFor the fabrication of PSCs, the ITO-coated glass substrate was ultrasonicated in detergent, deionized water, acetone, and isopropanol for 15 min before being dried at 60 \\u00b0C. A TiO2 compact layer was prepared by spin-coating the dispersed TiO2 nanoparticle solution onto ITO at 5000 rpm for 40 s and dried at 150 \\u00b0C for 30 min. The MAPbI3 perovskite layer was fabricated using the spin-coating precursor solution (composed of 2.2 M MAI, 0.8 M PbAc2 and 0.2 M PbCl2 in 1 ml of DMF) at 3000 rpm for 40 s, followed by thermal annealing at 100 \\u00b0C for 10 min. For the preparation of the C60-PyP doped perovskite layer, a solution of C60-PyP in DMF was added into the perovskite precursor solution according to different weight ratios. To prepare the spiro-OMeTAD layer, 73.2 mg spiro-OMeTAD was first dissolved in 1 mL chlorobenzene; then, 28.8 mL of 4-tert-butyl pyridine and 18.8 mL of Li-TFSI solution (520 mg Li-TFSI in 1 mL acetonitrile) were added. The spiro-OMeTAD solution was spin-coated onto the CH3NH3PbI3 perovskite layer at 3000 rpm for 30 s to form a hole transport layer. Finally, the device was transferred into a vacuum chamber (10\\u20136 torr), and an Au electrode (ca. 100 nm thick) was thermally deposited through a shadow mask to define the effective active area of the device (0.10 cm2). All device fabrication procedures were carried out in a N2-purged glovebox (<0.1 ppm of O2 and H2O).\\n\\nThe current density\\u2013voltage (J\\u2013V) characterization was performed using a Keithley 2400 source measurement unit under simulated AM 1.5 irradiation (100 mW cm\\u22122) with a standard xenon-lamp-based solar simulator (Oriel Sol 3A, USA) which was calibrated with a mono-crystalline silicon reference cell (Oriel P/N 91150 V, with a KG-5 visible color filter) calibrated by the National Renewable Energy Laboratory (NREL). The scan speed for all of the J\\u2013V tests in this article was 100 mV s\\u22121. The measurements were performed with a mask (well-defined area size of 0.10 cm2) to ensure accurate measurement under ambient conditions. Around 15 devices were fabricated and measured independently under each experimental condition to confirm the reproducibility of the result and to obtain the statistical histograms of the photovoltaic parameters. The EQE measurements were carried out on an ORIEL Intelligent Quantum Efficiency (IQE) 200TM Measurement system established with a tunable light source. SEM measurements were carried out using a field-emission scanning electron microscope (Zeiss Gemini SEM 500, Germany). AFM images were recorded on an XE-7 scanning probe microscope in non-contact mode (Park systems, Korea). XPS measurements were performed on a Thermo ESCALAB 250 instrument with a monochromatized Al K\\u03b1 X-ray source in a vacuum. The X-ray diffraction (XRD) patterns were obtained on a Rigaku SmartLab X-ray diffractometer with Cu-K\\u03b1 radiation (0.154 nm). The GIXRD measurements were performed at the BL14B1 beamline of the Shanghai Synchrotron Radiation Facility (SSRF) employing an X-ray with a wavelength of 0.6887 \\u00c5. The two-dimensional GIXRD (2D-GIXRD) patterns were acquired using a MarCCD detector mounted vertically at a distance of around 365 mm from the sample with an exposure time of 30 s at a grazing incidence angle of 1\\u00b0. The 2D-GIXRD patterns were analyzed using software Fit 2D and displayed in scattering vector q coordinates with q = 4\\u03c0sin\\u03b8/\\u03bb, where \\u03b8 is half of the diffraction angle, and \\u03bb is the wavelength of the incident X-ray. The steady-state photoluminescence (PL) spectra were recorded employing an Edinburgh Instruments FLS920 fluorescence spectrometer with an excitation wavelength of 460 nm. Impedance spectroscopic measurements (EIS) were performed in the dark using an electrochemical workstation (Autolab 320, Metrohm, Switzerland) with a frequency range from 1 Hz to 1 MHz under 1.0 V. AC 20 mV perturbation was applied with a frequency from 1 MHz to 1 Hz. The obtained impedance spectra were fitted with Z-View software (v2.8b, Scribner Associates, USA). All the measurements were carried out in ambient surroundings.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (CH3NH3I) was synthesized via a previously reported method. Hydroxylamine hydrochloride (HONH3Cl) was obtained from Beijing Chemical Reagent Industrial Company. 2,2\\u2032,7,7\\u2032-Tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (spiro-OMeTAD) was purchased from Toronto Research Chemicals Inc. All other chemicals (PbI2, methylamine (CH3NH3), hydrogen iodide (HI), titanium isopropoxide, N,N-dimethylformamide (DMF), isopropanol (IPA), etc.) were purchased from Sigma Aldrich or Acros Organics and used as received without any purification. The conducting substrates were fluorine-doped tin oxide coated glass (FTO, 2.2 mm, 15 \\u03a9 per square, NSG, Japan).\\n\\nInitially, the patterned FTO, which were obtained by etching with 2 M HCl and Zn powder, were sequentially cleaned in an ultrasonic bath with detergent, deionized water, acetone, and isopropanol, respectively. After blow drying with clean nitrogen, the substrates were treated in oxygen plasma for 10 min.\\nThe PHJ-PSCs with device architecture of fluorine doped SnO2 (FTO)/compact TiO2 (C-TiO2)/CH3NH3PbI3/spiro-OMeTAD/Au (80 nm) were constructed according to the following step. The TiO2 compact layer (C-TiO2) was first deposited by spin-coating a mildly acidic solution of titanium isopropoxide in isopropanol (3000 rpm, 45 s) on the as-cleaned FTO substrates, then annealed at 500 \\u00b0C for 30 min. Before use, the as-prepared C-TiO2 substrates were immersed in 0.02 mM TiCl4 solution at 80 \\u00b0C for 30 min. Finally, the films were sintered at 500 \\u00b0C for 30 min after rinsing with deionized water and ethanol.\\nThe CH3NH3PbI3 films were prepared via one-step precursor solution spin-coating deposition (OPSSD) in a glovebox with N2 atmosphere. 47 wt% of the perovskite precursor solution without additive was obtained by dissolving PbI2 and CH3NH3I (with molar ratio of 1:1) into anhydrous DMF. To achieve the ternary mixture solution doped with HONH3Cl, a proper amount of HONH3Cl was added into the above binary mixture solution of PbI2 and CH3NH3I (with molar ratio of 1:1) into DMF. After that, the as-prepared mixture solutions were continuously stirred and heated at 70 \\u00b0C for 12 h in the dark. For perovskite film preparation, the above-mentioned mixture precursor solutions were spin-coated onto the FTO/C-TiO2 substrates with a speed of 5000 rpm for 45 min. Thereafter, the as-constructed films were annealed at 110 \\u00b0C for 20 min onto the hot plate. After the films were cooled to room-temperature, 20 \\u00b5L of HTM solution was dropped onto the CH3NH3PbI3 perovskite layer and spin-coated at 4000 rpm for 30 s. The HTM solution was prepared via dissolving 72.3 mg of 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene(spiro-MeOTAD) in 1 mL of anhydrous chlorobenzene, then 30 \\u00b5L of 4-tert-butylpyridine (TBP) and 18 \\u00b5L of lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg of LI-TSFI in 1 mL of acetonitrile) were added as additives under energetic stirring. The devices were then left in a dry air atmosphere with low relative humidity in the dark for spiro-MeOTAD oxidation. Finally, 80 nm of back contact electrodes were deposited via thermally evaporating Au on the top of the spiro-MeOTAD-coated devices under a pressure of ca. 1 \\u00d7 10\\u22126 Torr.\\n\\nInitially, it needs to be noted that all measurements for the films and devices were accomplished in open air (>45% relative humidity). X-ray diffraction characteristics were conducted using a Shimadzu XRD-6000 X-ray diffraction instrument with Cu-K\\u03b1 radiation. UV-vis absorption measurements were performed on a Japan Shimadzu model UV-2250 spectrophotometer. Steady-state (Ss) and time-resolved (Tr) photoluminescence measurements were carried out via an FLS 920 luminescence spectrometer with an excitation wavelength of 425 nm which passed through a 650 nm low-pass filter. The annealing temperature of all samples was set at 110 \\u00b0C for a period of 20 min. Especially, the samples for XRD and PL characterization were prepared by directly spin-coating the precursor solutions on clean glass slides. Scanning electron microscope (SEM) images were recorded using a Rili SU 8000HSD Series Hitachi New Generation Cold Field Emission SEM. Elemental analysis and distribution measurement was performed with SEM (Rili SU 8000HSD) and an energy dispersive spectrometer (EDS).\\nThe photocurrent and voltage properties of the PSCs were characterized using a CHI660D electrochemical workstation by applying an external bias potential to the solar cells under simulated AM 1.5G sunlight (100 mW cm\\u22122) generated from an AAA Class 150 W solar simulator (SAN-EI ELECTRIC, model XES-40S2-CE, Japan) with an AM 1.5G type filter. The light intensity was calibrated using a Newport Oriel PV standard reference cell and meter (model 91150 V); the photoactive area of the solar cells was 0.09 cm2 determined by a metal aperture, and the scan rate was 100 mV s\\u22121. The incident photon to electron conversion efficiency (IPCE) was measured using an IPCE measurement system (model 2931-C, Newport, USA) using a 300 W xenon lamp (model 66902, Newport, USA) with a 1/4 monochromator (model 74125 Oriel Cornerstone 260, Newport, USA), and the light intensity was calibrated using a silicon detector (model 71675, Newport, USA).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 110,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Formamidine iodide (FAI) and methylammonium bromide (MABr) were obtained from Xi\\u2019an Polymer Light Technology Corp. Other materials were purchased from Alfa. All materials and reagents were used as received without further purification. FTO-coated glass was rinsed by sonication in detergent, and cleaned with ultrapure water and ethanol. A compact-TiO2 layer was deposited on the FTO by spray pyrolysis at 430 \\u00b0C. The precursor solution was composed of 0.6 mL of titanium diisopropoxide and 0.4 mL of bis(acetylacetonate) in 7 mL of isopropanol. A mesoporous TiO2 layer was spin-coated on the compact layer at a speed of 4000 rpm for 20 s using a 30 nm TiO2 paste which was diluted with ethanol (TiO2:ethanol = 1:5.5). Next, mesoporous TiO2 was slowly annealed by sintering from room temperature to 510 \\u00b0C for 3 h on a flattening oven. The precursor solutions of 1.4 M Pb2+ in (FAPbI3)0.85(MAPbBr3)0.15 were obtained by dissolving the corresponding perovskite powders in DMF and DMSO mixed solvent (DMF:DMSO= 4:1 by volume) with stirring at 60 \\u00b0C for 30 min. In addition, the molar ratio of PbI2:FAI in the precursor solutions was 1.05:1. Then, the precursor solutions were spin-coated first at 1100 rpm for 11 s and then at 4600 rpm for 34 s in an air flowing glovebox. About 120 \\u03bcL of chlorobenzene was drop-cast on the substrate during the spin coating step 15 s before the end of the procedure. The substrate was then annealed at 105 \\u00b0C for 50 min on a hot plate. The precursor solutions of 1.4 M Pb2+ in (FEA)2PbI4 were obtained by dissolving FEAI and PbI2 in DMF and DMSO mixed solvent (DMSO:DMF= 1:4 by volume). The (FEA)2PbI4 film was prepared by spin-coating on a glass substrate with annealing at 105 \\u00b0C for 20 min. The FEAI interfacial modification solution with a concentration 0, 5, and 15 mg mL\\u22121 in isopropanol was spin-coated on the top of the perovskite absorber film at 3500 rpm for 20 s, and then the substrate was heated at 105 \\u00b0C for 20 min on a hot plate. The HTM solution with 73 mg of spiro-OMeTAD, 4-tert-butylpyridine, Li+ salt and cobalt(III) salt in chlorobenzene solvent was spin-coated onto the perovskite layer at 3000 rpm for 20 s. Finally, 60 nm of Au was deposited via thermal evaporation on top of the HTM layer.\\n\\nXRD patterns of the perovskite films were recorded on a Rigaku Smartlab 9 kW diffractometer with Cu K\\u03b1 radiation. The data were collected in the 2\\u03b8 range from 5\\u00b0 to 60\\u00b0 at room temperature. The film morphology was investigated by using a high-resolution scanning electron microscope (SEM) with a Schottky Field Emission gun. Atomic force microscopy (AFM) was carried out by using a MultiMode V (Veeco) viewer and analyzer. Absorption spectra and reflectance spectra were recorded on an ultraviolet-vis (UV-vis) spectrophotometer (U-3900H, HITACHI, Japan). Steady-state PL spectra were measured using a spectrofluorometer (Photon Technology International) and analyzed with the software Fluorescence. The J\\u2013V curves were measured by using a solar simulator (Newport, Oriel Class A, 91195A) with a source meter (Keithley 2420) under 100 mW cm\\u22122 illumination (AM 1.5G). The absorbed effective area for each device was 0.09 cm2 by masking a black mask. The incident photon to current efficiency (IPCE) was collected as a function of wavelength from 300 to 900 nm (PV Measurements, Inc.), with a dual Xenon/quartz halogen light source, measured in DC mode with no bias light used. The setup was calibrated with a certified silicon solar cell (Fraunhofer ISE) prior to measurements. The pump light wavelength was 500 nm and the probe light wavelength was 760 nm. At a repetition rate of 5 Hz, the energy of the laser device was 150 \\u03bcJ cm\\u22122. Electrochemical impedance spectroscopy (EIS) was recorded at \\u22120.8 V in the dark, in the frequency range of 1 Hz to 1 MHz by using an Autolab analyzer (Metrohm, PGSTAT 302N, Switzerland). The humidity stability test was carried out in a container with 50\\u00b1 5% relative humidity. The container was kept in the dark and the temperature was maintained at about 20 \\u00b0C.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55 | (FEA)2PbI4,\\n Perovskite_composition_short_form: FAMAPbBrI | (FEA)PbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 105.0 >> 105,\\n Perovskite_deposition_thermal_annealing_time: 50.0 >> 20.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbI2 (99.9985%), PbBr2 (99.9985%), 4-tert-butylpyridine (TBP) and bis(trifluoromethane) sulfonimide lithium salt (LiTFSI) were obtained from Sigma-Aldrich. N,N-dimethylformamide (DMF), dimethylsulfoxide (DMSO) and chlorobenzene were purchased from Alfa Aesar. Methylammonium bromide (MABr), methylammonium iodide (MAI) and formamidinium iodide (FAI) were purchased from Shanghai Materwin New Materials Co., Ltd. Spiro-OMeTAD was purchased from Luminescence Technology Corp, and triethylgallium (TEG) (99.9999%) was acquired from Nanjing Aimouyuan Scientific Equipment Co., Ltd. All these chemicals were used directly, without further purification. Laser-patterned FTO glass (Pilkington, 2.2 mm thick, sheet resistance = 15 \\u03a9 sq\\u22121) was sequentially cleaned with a mild detergent, distilled water and ethanol in an ultrasonic bath, and finally dried under a nitrogen stream.\\n\\nGaN thin films were deposited on FTO glass substrates using an Angstrom-dep III PEALD reactor (Thin Film Technologies Ltd., USA), equipped with an inductively coupled remote plasma (ICP) source. TEG is the Ga precursor, and a high-purity Ar/N2/H2 (1:3:6, 99.999%) plasma is the nitrogen source; high-purity Ar gas (99.999%) was used as the carrier gas for the precursor. The flow rates of both the carrier gas and the gas used in the plasma were set at 5 sccm, and the radio-frequency (RF) power and plasma frequency were 60 W and 13.56 MHZ, respectively. Cleaned FTO glass substrates were put on the reactor chuck in the PEALD system and pumped down to the system base pressure of \\u223c0.15 Torr, then the substrate chuck was heated to the growth temperature and left to equilibrate for 20 min. Initially, 5 plasma cycles were run to remove any residual oxygen from the surface. An ALD-GaN cycle consisted of a plasma exposure for 30 s and a purge for 30 s, followed by a TEG dose for 0.5 s and a reaction time of 45 s, and then a purge for 30 s. As indicated, for one ALD-GaN cycle, the exposure times used for TEG and plasma were set at 0.5 s and 30 s, respectively, and pumping gas times of 30 s were required in between for purging the excess TEG and H2O. A growth rate per cycle (GPC) of \\u223c1.0 \\u00c5 was determined by in situ spectroscopic ellipsometry (SE) for the thin films grown on FTO glass at 280 \\u00b0C. Compact GaN layers with various thicknesses (10, 30, 50 and 80 PEALD cycles) were used to fabricate planar PSC devices.\\n\\nThe fabrication method used for the PSCs was very similar to that reported in our previous work. Specifically, an FA0.85MA0.15Pb(I0.85Br0.15)3 perovskite light absorber was deposited on the top of the GaN film by using a perovskite precursor solution prepared by mixing different molar quantities of 1.32 M PbI2, 0.12 M PbBr2, 1.08 M FAI, 0.24 M MAI and 0.12 M MABr solutions in 1 L of solvent with a 4:1 volume ratio of DMF and DMSO. The perovskite films were fabricated by a one-step anti-solvent method, that is, the perovskite precursor solution was dropped onto the GaN layer and spin-coated at 1000 rpm for 10 s and 5000 rpm for 30 s; 150 \\u03bcL of chlorobenzene solution was dripped onto the spinning substrate at 15 s during the high speed step. The as-prepared films were heated at 150 \\u00b0C in a N2 atmosphere for 10 min and then at 100 \\u00b0C in a vacuum for 40 min. A 200 nm-thick spiro-OMeTAD layer was spin coated onto the top of the perovskite film at a speed of 3000 rpm, then heated at 60 \\u00b0C for 5 min. The perovskite film fabrication process was carried out in a glovebox. Finally, an Au electrode about 80 nm thickness was deposited by thermal evaporation under a vacuum of 10\\u22127 Torr.\\n\\nAtomic force microscopy (AFM) measurements were carried out using a Bruker Dimension Icon instrument. Scanning electron microscopy (SEM) images were obtained using a Hitachi S-4800 SEM. Absorption and transmittance spectra were measured using a UV-vis spectrophotometer (UV-2550, Shimadzu) that covers wavelengths ranging from 300 nm to 850 nm. X-ray diffraction (XRD) measurements of the GaN films were carried out using a Smartlab GIXRD. X-ray photoelectron spectroscopy (XPS) data were acquired using a Thermo Escalab 250Xi instrument. Contact angles were measured by using an OCA25, DataPhysics instrument. Hall measurements were performed by using a Phys Tech RH 2030 system at room temperature, under a DC magnetic field of 0.39 T. The valence band (VB) spectra were measured with a monochromatic HeI light source (21.2 eV) and a VG Scienta R4000 analyser. A sample bias of \\u221210 V was applied to observe the secondary electron cut-offs (SEC). The work functions (\\u03a6) were determined from the difference between the photon energy and the binding energy of the secondary cutoff edge. Current\\u2013voltage (J\\u2013V) curves were measured under AM 1.5 simulated sunlight (100 mW cm\\u22122) from a Zolix SS150A lamp that was calibrated with a standard silicon reference cell, and recorded using a digital source meter (Keithley model 2602). The solar cells were masked with a black aperture to define an active area of 0.1 cm2, and the J\\u2013V curves were measured during a forward bias scan going from \\u22120.05 to 1.1 V and a reverse scan from 1.1 to \\u22120.05 V at a scan rate of 30 mV s\\u22121. Incident photon-to-electron conversion efficiencies (IPCE) were measured using a lab-made setup with the wavelength ranging from 350 nm to 850 nm. Steady-state photoluminescence (PL) spectra were measured using a PL spectrometer (Edinburgh Instruments, FLS 900) with a xenon lamp as the excitation source. The transient PL spectra were measured with the same instrument together with a pulsed diode laser (EPL-445, 0.8 \\u03bcJ cm\\u22122) run at a pulse frequency of 1 MHz. The electrochemical impedance spectra (EIS) were measured using a Zahner IM6e electrochemical workstation in the dark in the frequency range from 0.1 to 106 Hz at a bias voltage of 0.8 V.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: GAN,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: ALD,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were procured from Sigma Aldrich and used as such; PbI2 was obtained from TCI, while MAI and FAI were procured from Dyesol and employed without any treatment or purification. 2,2\\u2032,7,7\\u2032-Tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (Spiro-OMeTAD) was acquired from Merck KGaA.\\nPerovskite based solar cells (PSCs) were fabricated on FTO-coated glass (TEC15, Pilkington) pre-patterned by laser etching. Prior to usage (perovskite deposition), the substrates were cleaned using Hellmanex\\u00ae solution and rinsed with deionized water and ethanol. Following this, the samples were ultrasonicated in acetone, rinsed using 2-propanol and dried by using compressed air. A TiO2 compact layer was deposited by spray pyrolysis at 450 \\u00b0C using a titanium diisopropoxide-bis(acetyl acetonate) precursor solution (75% in 2-propanol, Sigma Aldrich) using dry air as a carrier gas. The TiO2 blocking layer was then annealed for 30 minutes at 450 \\u00b0C for the formation of the anatase phase. Once samples reached ambient temperature, a TiO2 mesoporous layer (Dyesol, 30NRD) was deposited by spin-coating (4000 rpm for 20 s), and the samples were annealed progressively at 450 \\u00b0C. Subsequently a 1.2 M mixed cation perovskite ((FAPbI3)0.85(MAPbBr3)0.15) layer was then deposited, by a one-step method. The perovskite solution was spin-coated in two steps: at 1000 and 6000 rpm for 10 and 20 s respectively. In the second step, 100 \\u03bcL of chlorobenzene was dropped onto the spinning substrate (during the last 15 seconds) as an anti-solvent approach. The samples were then annealed at 100 \\u00b0C for 1 h in an argon filled glove box. For the triple cation based perovskite (Cs/FA/MA), CsI was separately dissolved (1.5 M stock solution in dimethyl sulfoxide (DMSO)), and added to the mixed perovskite precursor to achieve the desired composition (5% and 10%).\\nOnce the perovskite film was annealed and left to cool down, 35 \\u03bcL of a Spiro-OMeTAD solution was then deposited by spin-coating at 4000 rpm for 20 seconds as the hole transport material. The Spiro-OMeTAD material (72.3 mg) was dissolved in 1 mL of chlorobenzene by using additives: 17.5 \\u03bcL of a lithium bis(trifluoromethylsulphonyl)imide (LiTFSI) stock solution (520 mg of LiTFSI in 1 mL of acetonitrile), 21.9 \\u03bcL of a FK209 (tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III)tris(bis(trifluoromethylsulfonyl)imide)) stock solution (400 mg in 1 mL of acetonitrile) and 28.8 \\u03bcL of 4-tert-butylpyridine (t-BP). Finally, 80 nm of gold was deposited as a metallic contact by thermal evaporation at a vacuum level of between 1 \\u00d7 10\\u22126 and 1 \\u00d7 10\\u22125 torr. All the solutions were prepared inside an argon filled glove box under controlled moisture and oxygen conditions (H2O level: <1 ppm and O2 level: <10 ppm).\\n\\nThe transmittance and reflectance spectra of the perovskite films were collected using a Cary 60 spectrophotometer. Current density\\u2013voltage (J\\u2013V) curves were documented with a Keithley 2400 source-measurement-unit under AM 1.5 G, 100 mW cm2 illumination from a 450 W AAA solar simulator (ORIEL, 94023 A). This was calibrated using a NREL certified calibrated mono-crystalline silicon solar cell. A black metal mask (0.16 cm2) was used over the square solar cell active area (0.5 cm2) to reduce the influence of scattered light.\\nPhotovoltaic parameters including JSC, VOC, fill factor (FF), and power conversion efficiency (PCE) were extracted from the photocurrent\\u2013voltage (J\\u2013V) curves of the solar cells. The scan rate and the active surface area used for measuring the devices were optimized as such to calculate the real value for efficiencies without having a hysteresis effect. (Active surface area: 0.16 cm2, scan rate: 100 mV s\\u22121, pre-sweep delay: 20 s). The IPCE measurements were performed using a Newport 150 W xenon lamp coupled to an Oriel Cornerstone 260 motorized \\u00bc m monochromator as the light source, and a 2936-R power meter to measure the short circuit current.\\nFor X-ray photoelectron spectroscopy (XPS) characterization, films were prepared by spin-coating the perovskites onto FTO glass. For XPS, an Omicron Nanotechnology GmbH system operating at a base pressure of \\u223c6 \\u00d7 10\\u221211 Torr with a non-monochromatized Mg K\\u03b1 line at 1253.6 eV was used. The acquired resolution of core levels was 0.1 eV measured at 90% of peak height and the spectra were acquired at 25 eV pass energy. The survey spectra were acquired with 100 eV pass energy, and the resolution is 1 eV. An EKF 300 ion source, operating at a pressure of 1.6 \\u00d7 10\\u22125 mbar, was used for depth-profiling and sputtering and it was effected by an Ar+ ion beam energy of 0.5 kV. The target current was 59.3 \\u03bcA, and the sputtering time was 5 min. The sputtering rates employed were small enough to remove the top layers. The core level spectra were deconvoluted using a non-linear iterative least squares Gaussian fitting procedure. For all fitting multiplets, the FWHMs were fixed accordingly. Corrections due to charging effects were taken care of by using C(1s) as an internal reference and the Fermi edge of a gold sample. The Jandel Peak FitTM (version 4.01) program was used for the analysis. XRD patterns were recorded on a Rigaku powder diffractometer using a CuK\\u03b1 source. The wavelength range of the UV lamp used was between 250 and 365 nm and the samples were kept in an ambient atmosphere (55\\u201360% RH) in our lab. Absorption spectra were recorded for the perovskites by using an Agilent Carry 60 spectrophotometer. The ETM, absorber and HTM layer thicknesses were 150, 480 and 270 nm respectively.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI, 99.99%, LT-S9126) was purchased from Luminescence Technology Corp., PbI2 (99%) from Sigma Aldrich, and poly(3-hexylthiophene) (P3HT) from Rieke Metals. The indium tin oxide (ITO) coated glass was supplied by Fine Chemicals (South Korea) (15 \\u03a9 per square sheet resistance, and 0.7 mm thickness). Anhydrous chlorobenzene (CB, 99.9%), dimethylformamide (DFM, ACS reagent \\u2265 99.8%), and dimethyl sulfoxide (DMSO, \\u226599.9%) were from Sigma Aldrich. Gold (Au) was from Vacuum Thin Film Materials Co. (South Korea). Zinc acetate dihydrate (99.999%), monoethanolamine (MEA, ACS reagent, 99.0%), and 2-methoxyethanol (2-ME, anhydrous, 99.8%) were from Sigma Aldrich. The vapor pressures of the solvents, the decomposition temperature, and the melting points of solid materials come from safety data sheets of Sigma Aldrich.\\n\\n(1) 50 wt% perovskite solution of MAI:PbI2:DMSO 1:1:0.6. 0.161 g MAI and 0.472 g PbI2 were dissolved in 0.600 ml DMF and 0.0434 ml DMSO, and stirred at 1500 rpm and 65 \\u00b0C on a hotplate overnight. A yellow and turbid solution was obtained. The recipes of other perovskite precursor solutions are as similar as this recipes but with different component ratios. (2) P3HT solution: 0.015 g P3HT in 1 ml chlorobenzene was stirred at room temperature overnight. (3) ZnO solution: the 0.5 M precursor solution consisting of 0.220 g zinc acetate dihydrate and 61.0 \\u03bcl monoethanolamine in 2 ml 2-methoxyethanol was stirred at room temperature overnight.\\n\\nThe ITO substrates were ultra-sonicated for 15 min in deionized water, followed by acetone, and then isopropyl alcohol (IPA). All the cleaned ITO substrates were dried in an oven at 75 \\u00b0C for 30 min, and then kept overnight. The ZnO 0.5 M precursor solution after filtering was spin-coated on the ITO substrates at 4000 rpm for 40 s. The wet ZnO films were annealed at 160 \\u00b0C in the oven for 10 min. 50 nm dense ZnO films were obtained. The spin coating of 50 wt% perovskite solution filtered with PVDF filter was carried out in a special dynamic mode. The dynamic spin-coating process was involved first starting the substrate spinning, and allowing it to reach the desired spin speed, before the perovskite solution was dispersed onto the ZnO substrate. 35 \\u03bcl of perovskite solution was dripped onto the ZnO coated substrate by the dynamic spin-coating process, and the washing treatment with CB of 200 \\u03bcl was carried out by pipette tips during the rotation of perovskite coating, 5 s after starting the dripping of perovskite solution. All the wet light red perovskite films were annealed at 90 \\u00b0C, for 60 min. 50 \\u03bcl P3HT solution, 15 mg ml\\u22121 in CB, was spin-coated on the perovskite film at 2000 rpm for 25 s. Finally, Au electrode was deposited by thermal evaporator. After the thermal deposition of \\u223c50 nm thick Au film through a shadow mask, the devices were finished for measurement. All fabrication processes were carried out in ambient air. The active area of each device was 0.1 cm2.\\n\\nThe current density\\u2013voltage (J\\u2013V) characterization of the devices was measured by J\\u2013V curve tracer (Eko MP-160) and solar simulator (Yss-E40, Yamashita Denso) under AM 1.5G irradiation with the intensity of 100 mW cm\\u22122, calibrated by a Newport certified standard silicon cell. Fourier transform infrared spectra (FT-IR) were scanned with a resolution of 8 cm\\u22121 by Bruker IFS-66/S FTIR. Optical microscopy images were obtained using an Olympus BX51 Microscope Digital Camera. Atomic force microscopy (AFM) images were obtained with advanced scanning probe microscopes (PSIA Corp). The thicknesses of all films were characterized by the AFM system.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Unknown,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The CH3NH3PbI3 thin films were prepared via a one-step process as reported in the literature. The perovskite precursor solution was prepared by dissolving PbI2 (99%, Sigma-Aldrich) and CH3NH3I (99%, Shanghai MaterWin New Materials Co., Ltd) in 1 ml anhydrous N,N-dimethylformamide (DMF) in a molar ratio of 1:1. Subsequently, the as-prepared precursor solution was kept at 60 \\u00b0C overnight. After cooling down to room temperature, 0.1 mL hydrogen iodide (HI) with a concentration of 100 \\u03bcL mL was added into the solution and stirred for 30 min. The CH3NH3PbI3 perovskite thin films were obtained by spin-coating the mixed precursor solution onto clean TiO2 coated FTO (Zhuhai Kaivo Optoelectronic Technology Co., Ltd) at 3000 rpm for 30 s, and subsequently annealed at 100 \\u00b0C for 20 min in a glove box under argon atmosphere.\\nThe microstructures of the as-prepared perovskite films were investigated by GIXRD performed at the BL14B1 beamline of the Shanghai Synchrotron Radiation Facility (SSRF) using X-ray with a wavelength of 1.24 \\u00c5 at a grazing incidence angle of 0.2\\u00b0. The GIXRD patterns were collected by using a MarCCD 225 detector with a sample\\u2013detector distance of 160 mm, which will be presented later in q coordinates using the equation q = 4\\u03c0sin\\u03b8/\\u03bb, where \\u03b8 is half of the diffraction angle and the \\u03bb of 1.24 \\u00c5 is the wavelength of X-rays with a photon energy of 10 keV. In the present GIXRD data, q has been calibrated by measuring the XRD of a lanthanum hexaboride reference sample. The SEM images of the films were taken by using a high resolution electron beam lithography system (CABL-9000C).\\nFor photoemission experiments, the as-prepared perovskite films were transferred into an ultrahigh vacuum (UHV) system with a base pressure better than 2 \\u00d7 10\\u221210 mbar and kept in vacuum overnight for degassing at 100 \\u00b0C. After being degassed, rubrene molecules (99.9%, Sigma-Aldrich) were deposited onto perovskite substrates using a standard Knudsen-cell. Photoemission measurements were performed in situ at room temperature after each deposition using a PHOIBOS 100 analyzer together with a monochromatic X-ray source (Al K\\u03b1: 1486.61 eV) for XPS and a helium light lamp (He I: 21.2 eV) for UPS, respectively. Using a gold reference sample, the instrumental energy resolution for XPS and UPS was estimated to be 0.45 eV and 15 meV, respectively. The rubrene film thicknesses were calibrated by the attenuation of Pb 4f7/2 XPS intensities from the perovskite substrates after each deposition. To extract the WF from the SECO in the UPS spectra, a \\u221210 V bias was applied to the samples. All photoemission spectra were collected at normal emission, and the binding energy was referred to the Fermi level of a sputter-cleaned gold foil electrically connected to the sample. The least-squares peak fit analysis of XPS spectra was performed by using the XPSpeak software.\\nRubrene/perovskite based solar cells were fabricated by constructing the inverted planar device architecture of Ag/PCBM/CH3NH3PbI3/rubrene/ITO. Rubrene was dissolved in toluene at a concentration of 10 mg mL\\u22121 and stirred overnight at room temperature. The rubrene solution was spin-coated on a plasma-cleaned and patterned ITO substrate at 1200 rpm for 60 s. After baking at 150 \\u00b0C for 1 hour for the formation of rubrene thin films (\\u223c20 nm), the perovskite precursor solution (HI added) was spin-coated on the rubrene/ITO substrate and subsequently annealed at 100 \\u00b0C for 2 min to form perovskite films (see for detailed information). The rubrene film thickness of \\u223c20 nm was chosen according to . After the formation of perovskite films (350 nm), PCBM (40 nm, 99%, Sigma) used as the electron transport layer was deposited by spin-coating the PCBM precursor solution (10 mg mL\\u22121 dissolved in chlorobenzene) at 2000 rpm for 45 s. Finally, the films were transferred into a thermal evaporation chamber for Ag electrode (100 nm) deposition. The fabrication procedures were carried out in a nitrogen-filled glove box (<0.1 ppm O2 and H2O). For comparison, we fabricated inverted planar solar cell devices using PEDOT:PSS (Sigma) films as HTLs instead of rubrene thin films. We also fabricated devices by forming rubrene films (\\u223c20 nm) on top of PEDOT:PSS films to further improve the rubrene film quality prepared by spin-coating. The efficiency and J\\u2013V curves characteristics were measured under AM 1.5G illumination at 100 mW cm\\u22122 using a Keithley 2400 sourcemeter. The EQE spectrum was measured by using a power source (150W Xenon lamp) with a monochromator (MonoRa-500i: DONGWOO OPTRON Co., Ltd) and a potentiostat (IviumStat: IVIU).\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Undoped,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: HI,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: Rubrene | PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: Undoped,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: ,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FAI. Formamidine acetate (0.1 mol, 98%, Sinopharm) and hydriodic acid (0.1 mol, 57 wt% in water, sigma-aldrich) were reacted stoichiometrically and were stirred at 0 \\u00b0C for 2 h. By rotary evaporation of the solvent at 60 \\u00b0C under reduced pressure, a primrose yellow powder was obtained. Then it was recrystallized twice by dissolving in ethanol, cleaned using diethyl ether and collected by filtration. Finally, the product was completely dried at 60 \\u00b0C in a vacuum oven for 12 h.\\nHOCH2CH2NH3I (EAI). Hydroiodic acid (0.1 mol, 57 wt% in water, sigma-aldrich) reacted with ethanolamine (0.1 mol, 99%, Sinopharm) for about 2 h with constant stirring; the subsequent preparation steps are the same as above.\\n\\nFTO-coated glass was sonicated using detergent and ultrapure water, and then rinsed three times with ultrapure water and ethanol. By spray pyrolysis at 430 \\u00b0C, a compact TiO2 layer which was composed with 0.4 mL bis(acetylacetonate) and 0.6 mL titanium diisopropoxide in 8 mL isopropanol was coated on the FTO. The TiO2 paste (30 nm, dyesol) was diluted with ethanol (TiO2:ethanol = 1:5.5 by weight), and then it was spin-coated on the compact layer at 4000 rpm for 20 s. After the spin coating, the substrate was slowly sintered from room temperature to 510 \\u00b0C for 3 h on a flattening oven. 1.4 M (Pb2+) perovskite precursor solutions were obtained by dissolving the stoichiometrically corresponding perovskite powders (FAPbI3)0.85(MAPbBr3)0.15 and [(HOCH2CH2NH3)2PbI4]x[(FAPbI3)0.85\\u2013(MAPbBr3)0.15]1\\u2212x into the DMSO and DMF mixed solvent (DMF:DMSO = 4:1 by volume). Before using, the precursor solutions were stirred at 60 \\u00b0C for 1 h. Then, the precursors were spin-coated on the substrate first at 1100 rpm for 11 s and second at 4600 rpm for 33 s in an air flowing glovebox with less than 20% RH. Chlorobenzene of 120 \\u03bcL as an anti-solvent was drop-cast on the perovskite layer during the spin coating step 15 s before the end of the procedure. The perovskites were annealed at 105 \\u00b0C for 60 min on a heating platform. The HTM solution which was composed of 73 mg spiro-OMeTAD, 4-tert-butylpyridine, and Li+ salt and cobalt(III) salt in 1 mL chlorobenzene was spin-coated at 3000 rpm for 20 s on the perovskite layer. Finally, via thermal evaporating, 60 nm of Au was deposited on the HTM layer.\\n\\nXRD patterns of the perovskite and the MD perovskite films were performed on an X'Pert MPD PRO (PANalytical). The 2\\u03b8 range was 5\\u201370\\u00b0 at room temperature. The perovskite and the MD perovskite films morphology was recorded using a high-resolution field-emission scanning electron microscope (FE-SEM, sirion200, FEI Corp., Holland) with a Schottky field emission gun. Ultraviolet-visible (UV-VIS) absorption spectra were studied using an ultraviolet-vis (UV-vis) spectrophotometer (U-3900H, HITACHI, Japan). The wavelength range was from 300 nm to 900 nm. Steady-state PL spectra were performed on a spectrofluorometer (photon technology international) and analyzed by the software Fluorescence. A standard 450 W xenon CW lamp with an exciting wavelength of 473 nm was used to excite the samples. J\\u2013V curves were collected using a solar simulator (Newport, Oriel Class A, 91195A) with a source meter (Keithley 2420) at 100 mW cm\\u22122 illumination AM 1.5G. A certified silicon solar cell (Fraunhofer ISE) was used to calibrate the setup before the measurements. By masking the device using a black mask , the active area was kept at 0.09 cm2. Incident photon to current efficiency (IPCE) was measured with a dual xenon/quartz halogen light source (PV Measurements, Inc.), and tested in the DC mode with no bias light used. The wavelength range was from 300 nm to 900 nm. Transient absorption (TA) spectra were recorded on an LKS (Applied Photophysics). The probe light wavelength of the sample was 760 nm by using a laser light wavelength of 500 nm. The energy of the laser device was 150 \\u03bcJ cm\\u22122 with a repetition rate of 5 Hz. Electrochemical impedance spectroscopy (EIS) was measured at \\u22121.0 V using an Autolab analyzer (Metrohm, PGSTAT 302N, Switzerland) in the dark and the frequency range was from 1 Hz to1 MHz.\\n\\nHeat aging test was done in a container at 85 \\u00b0C. The container was set at less than 10% RH in the dark. A UV aging test was performed in a container with UV irradiation. The temperature of the container was maintained at 20 to 30 \\u00b0C using a cooling system and the humidity was set at about 15% RH. The wavelength of the UV light source (UV-Hg-2000, Beijing Lighting Research Institute) was about 360 nm. When the sample was placed at 50 cm from the light source, the UV light source produced about 3\\u20134 times the amount of UV light in the AM 1.5G spectrum. Humidity aging test was performed in the dark inside of a container with 40\\u201350% RH. The temperature of the container was kept at about 20 \\u00b0C.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15Pb1.0Br0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: EAI,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 105,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"First, laser-patterned, FTO-coated glass substrates (TEC15, Pilkington) were cleaned by ultrasonication in an alkaline aqueous washing solution, rinsed with deionized water, ethanol and acetone, and subjected to treatment with O3 for 30 min. A 20\\u201340 nm thick compact layer of TiO2 was then deposited on the substrates by spin-coating of 0.15 M and 0.3 M commercial solutions of titanium diisopropoxidebis(acetylacetonate) (75% in 2-propanol, Sigma-Aldrich) diluted in ethanol (1:39 volume ratio) as a precursor and subsequently annealed in air at 450 \\u00b0C for 30 min. After cooling to room temperature, the substrates were treated in a 0.04 M aqueous solution of TiCl4 for 30 min at 70 \\u00b0C, rinsed with deionized water and dried at 500 \\u00b0C for 20 min.\\n\\nA layer of mp-TiO2 composed of particles with a size of 20 nm was deposited by spin-coating at 4000 rpm for 15 s using commercial TiO2 paste (Dyesol 18NRT, Dyesol) diluted in ethanol (2:7 weight ratio). For the incorporation of metallic nanoparticles, HAuCl4\\u00b73H2O was directly added to the mp-TiO2 solution and spin-coated on a FTO/Bl-TiO2 substrate. After drying at 125 \\u00b0C, the TiO2 films were gradually heated to 500 \\u00b0C, baked at this temperature for 15 min and cooled to room temperature. However, this method is not convenient for the synthesis of Au nanoparticles with mp-TiO2. Therefore, we have followed the method of synthesizing Au nanoparticles.\\n\\nInitially, Au NPs were synthesized by a chemical route. In typical experiments, a 1 mM aqueous solution of hydrogen tetrachloroaurate(III) trihydrate (HAuCl4\\u00b73H2O) was boiled for 30 min under reflux. About 2.5 mL of a 1% w/w aqueous solution of trisodium citrate dihydrate was added simultaneously under magnetic stirring over a period of 20 min. The obtained clear red solution was slowly cooled to room temperature. About 2.5 mL of a 5% solution of polyvinylpyrrolidone (PVP) in deionized water was added to the abovementioned red solution and further stirred for 12 h at room temperature. Then, the solution was centrifuged at 10000 rpm for 30 min and the synthesized Au NP dispersed in ethanol. The desired amount of this solution of Au NP was mixed with commercial mp-TiO2/ethanol paste and spin-coated onto a FTO/Bl-TiO2 substrate. After drying at 125 \\u00b0C, the TiO2 films were gradually heated to 500 \\u00b0C, baked at this temperature for 15 min and cooled to room temperature. The film with deposited mp-TiO2 and Au@mp-TiO2 was again treated with TiCl4.\\n\\nChemicals and materials. Polyvinylpyrrolidone (PVP) (PVP K90, MW = 130000), ethanol (Daejung), titanium(IV) isopropoxide (Ti(OiPr)4, Junsei) and acetic acid (Kanto Chemical) were used as initial precursors for the deposition of nanofibers. All these chemicals were used without further purification.\\nPreparation of TiO2 feeding solution. In a typical experiment, 3 g PVP was dissolved in 27 g ethanol under vigorous stirring. Then, a 6 mL solution of Ti(OiPr)4 was dissolved in an equal volume of acetic acid and ethanol. These two solutions were kept separately for constant stirring for 24 h. The clear solution of Ti(OiPr)4 was mixed with the ethanolic solution of PVP drop by drop and finally stirred for a further 5 h to obtain a colloidal solution.\\nPreparation of TiO2 and Au@TiO2 nanofibers. The abovementioned prepared electrospinning solution was carefully sucked into a 5 mL glass syringe and fixed horizontally arranged electrospinning equipment (SGE Analytical Science). The positive electrode was connected to the needle of the syringe containing the precursor solution. The drum rotating speed (400 rpm) and the distance between the anode and cathode (15 cm) were kept constant. The spinning rate was kept at 1.0 mL h\\u22121 by a syringe pump (KDS-100, KD Scientific). For the incorporation of metallic nanoparticles, HAuCl4\\u00b73H2O was added to the electrospinning solutions and the solutions were then instantly loaded into a syringe. Au-embedded TiO2 nanofibers of different compositions were synthesized by the addition of various amounts of HAuCl4\\u00b73H2O to the TiO2-PVP precursor solution at loading ratios of 0.1 wt% to 0.6 wt%. In this investigation, we added different quantities of a solution of HAuCl4\\u00b73H2O (0.0042, 0.0084, 0.0126, 0.0168, 0.0210, and 0.0252 g) to 3 mL TiO2-PVP precursor solution to deposit TiO2 nanofibers. These nanofibers were further used for perovskite solar cells and new results for Au nanoparticles versus TiO2 nanofibers have been added in a revised manuscript. At this point, an electric field potential of 9 kV was applied between the needle tip and a grounded substrate at a distance of 15 cm. Finally, after heat treatment at 500 \\u00b0C for 3 h in air, reflective white and bluish Au-embedded TiO2 nanofibers (Au@TiO2 nanofibers) were obtained (ESI Fig. S12\\u2020). The temperature of thermal annealing was optimized by TGA analysis (ESI Fig. S13\\u2020). The crystallinity and composition of the nanofibers were confirmed by XRD, SEM, TEM and EDS mapping analysis (ESI Fig. S14, Fig. S15, and Fig. S16\\u2020). A paste of synthesized bare and Au@TiO2 nanofibers was prepared using terpineol and ethyl cellulose in an ethanol solvent and used for spin-coating.\\nPreparation of methylammonium lead iodide (MAPbI3). Methylammonium iodide (MAI) was synthesized by the dropwise addition of hydriodic acid (aqueous, 57 wt%, Sigma-Aldrich) to a solution of methylamine (aqueous, 40 wt%, TCI Chemicals) in an ice bath. The ice-cold solution was stirred for 2 h and the solvent was evaporated using a rotary evaporator (95 mbar vacuum, 400 rpm rotation). The white product was dissolved in ethanol and recrystallized using diethyl ether. Fresh white crystals were washed three times using diethyl ether and dried in a vacuum for 24 h. The resulting white solid product was further used for the synthesis of MAPbI3.\\nThe MAPbI3 precursor solution was prepared by dissolving equimolar amounts of MAI and lead iodide (PbI2) (Aldrich, 99.999%) in anhydrous \\u03b3-butyrolactone (40% by weight, Sigma-Aldrich) at 70 \\u00b0C and stirred for 12 h. The prepared yellow solution was further filtered twice using a syringe filter (Whatman GD/X PVDF, pore size 0.45 \\u03bcm). The clear yellow solution was dripped on top of a mp-TiO2 film and the film was soaked for 1 min and then spun at 2000 rpm for 45 s and 3000 rpm for 45 s at one ramp rate. The film was placed on a hotplate at 95 \\u00b0C for 10 min to form dark brown crystalline MAPbI3. We investigated and optimized the best performance based on measurements from thermogravimetric analysis (ESI Fig. S17\\u2020).\\nThe hole-transport material (HTM) was prepared by a standard procedure reported elsewhere with a few modifications. A total of 180 mg 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamino)-9,9\\u2032-spirobifluorene (spiro-MeOTAD, Merck) was dissolved in 1 mL chlorobenzene (99.8%, Aldrich) with the addition of 37.5 \\u03bcL bis(trifluoromethane)sulfonimide lithium salt (LiTFSI, 99.95%, Aldrich) (170 mg mL\\u22121) in acetonitrile and 17.5 \\u03bcL 4-tert-butylpyridine (TBP, 96%, Aldrich). (Please note that HTM is not stable for a long time; therefore, we prepared a fresh solution of HTM before each experiment.) The MAPbI3 + TiO2 composite films were coated with HTM solution using a spin-coating method at 3000 rpm for 30s. We took precautions for proper pore filling. Then the substrates were transferred to a vacuum chamber and evacuated to a pressure of 2 \\u00d7 10\\u22126 mbar. For the counter electrode, an 80 nm thick layer of Au was deposited on the top of the HTM overlayer by thermal evaporation (growth rate \\u223c0.5 \\u00c5 s\\u22121). For comparison, we also prepared and characterized devices based on commercial P25 paste and Au@TiO2 (ESI Fig. S18, Fig. S19 and Fig. S20\\u2020). An XRD analysis of mp-TiO2 deposited on glass and FTO substrate is shown in Fig. S21.\\u2020 The active areas of all devices were 0.09 cm2 and measured without masking.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: nan | Au-np,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 95,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I, FAAc and PbI2 were bought from Xi\\u2019an Polymer Light Technology Corporation. Anhydrous N,N-dimethylformamide (DMF) and dimethylsulfoxide (DMSO) were purchased from Aladdin Reagent (China). PEDOT:PSS (Clevious PVP Al4083) was bought from H. C. Starck and phenyl-C61-butyric acid methyl ester (PCBM) was supplied by American Dye Sources. PTAA was bought from Derthon Optoelectronic Materials Science Technology. ITO glass substrates with a sheet resistance of 15 \\u03a9 sq\\u22121 were from Shenzhen Display (China).\\n\\nITO glass substrates were first cleaned with detergent, and then sequentially cleaned with acetone, ultrapure water, and isopropyl in an ultrasonic bath for 15 min, respectively. The ITO glass was dried with N2 and treated with O2 plasma for 10 min to improve the wettability. PEDOT:PSS was fabricated on the ITO substrates by spin-coating at 5000 rpm for 25 s, and then thermally treated at 140 \\u00b0C for 10 min. The substrates were taken into a glovebox filled with nitrogen. PTAA with a concentration of 5 mg mL\\u22121 dissolved in toluene was spin-coated on the ITO substrates at different speeds (3k, 4k, 5k and 6k rpm) for 40 s and then annealed at 105 \\u00b0C for 10 min. The CH3NH3PbI3 precursor solution was prepared by mixing CH3NH3I and PbI2 (1:1 molar ratio) into anhydrous DMF and DMSO (9:1 by volume), with a concentration of 1.2 M. The perovskite precursor solutions were stirred at room temperature overnight to promote dissolution of solid materials. The additive (0\\u201315 mol% FAAc) was added into the perovskite solution before spin-coating. A 0.45 \\u03bcm PTFE filter was used to filter the perovskite precursor solution before spin-coating. Specifically, the perovskite solution was spin coated onto PEDOT:PSS at 4000 rpm for 40 s. During spin coating, the perovskite surface was disposed by toluene to get high quality surface coverage as Seok reported. The perovskite films were annealed on a hot plate at 100 \\u00b0C for 10 min. A thin film of PCBM (circa 30 nm) was deposited onto the top of the perovskite layer with a concentration of 12 mg mL\\u22121 at a speed of 1500 rpm for 20 s. At the end, the samples were taken into a thermal evaporation chamber, where 100 nm Al was deposited. At the same time, the device area was defined as 0.1 cm2 for each cell by a shadow mask.\\n\\nThe thicknesses of the perovskite films were estimated using a Veeco Dektak150 surface profiler. The surface morphology of the films was characterized by scanning electron microscopy (SEM, Hitachi S-4800). The X-ray diffraction (XRD) patterns of the films were obtained with a Bruker D8 ADVANCE. Steady-state photoluminescence (PL) spectra were measured using a Fluoromax 4 spectrometer (HORIBA JobinYvon) with photoexcitation at 507 nm. The absorption spectra of the perovskite films on ITO glass were observed using a spectrophotometer (Varian Cary 50 UV/vis) in the range from 500 to 850 nm. Current\\u2013voltage (J\\u2013V) curves of devices were obtained under illumination of AM 1.5G through a Keithley 2420 source measurement unit, 100 mW cm\\u22122, with a Newport solar simulator. The light intensity was calibrated using a standard silicon solar cell. The scan rate of the reverse scan and forward scan was set to 0.1 V s\\u22121. A certified Newport incident photon conversion efficiency (IPCE) measurement system was used to analyze the external quantum efficiency (EQE) of the PSCs.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.05MA0.95PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: FAAc,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"A double-sided, polished, floating zone (FZ) 1\\u20135 \\u03a9 cm n-type \\u3008100\\u3009 Si wafer with a thickness of 300 \\u03bcm was used to prepare a bottom cell. A phosphorus (POCl3) diffused n++ (130.0 ohm sq\\u22121) high-low junction was formed on the rear side. A boron (BBr3) diffused p++ emitter (125.1 ohm sq\\u22121 to 15.1 ohm sq\\u22121) was formed on the front and was well defined to define the active area. The metal contact on the rear consists of Ti/Pd/Ag. The rest of the non-contacted rear was passivated by thermally grown and annealed SiO2. These polished silicon solar cells with an un-passivated p++ front were then directly used as a substrate for the fabrication of the top perovskite cell. To complete full tandem fabrication, the polished silicon solar cells were treated with a UVO cleaner for 6 min before SnO2 deposition. The SnO2 colloidal precursor (Alfa Aesar, tin(IV) oxide, 15% in H2O colloidal dispersion) was diluted with H2O to 3.75%. Then, the diluted SnO2 colloidal precursor was directly spin coated on the front of the silicon solar cells at 3000 rpm for 30 s, followed by baking on a hotplate at 150 \\u00b0C for 30 min in air to form a compact SnO2 ETL. After cooling down, the SnO2 coated silicon substrates were directly transferred to a N2 filled glovebox for the fabrication of the MAPbI3 absorber using a two-step method. Different concentrations of PbI2 precursor were prepared by dissolving PbI2 powder (Alfa Aesar) of different weight (461 mg, 553 mg and 737 mg) in 1 mL dimethylformamide (DMF) (Sigma-Aldrich) with excess dimethyl sulfoxide (DMSO) (Sigma-Aldrich, 71 \\u03bcL, 82 \\u03bcL and 114 \\u03bcL) which was then spin coated on the SnO2 coated silicon cell at 3000 rpm for 30 s. The MAI precursor (Greatcell Soalr) (dissolved in isopropyl alcohol (Sigma-Aldrich) at 40 mg mL\\u22121; 50 mg mL\\u22121; or 68 mg mL\\u22121) was then spin-coated at 3000 rpm for 30 s. The samples were dried at 100 \\u00b0C for 10 min producing dark brown dense MAPbI3 films with different thicknesses depending on the concentrations of precursors used.\\nFor the deposition of the hole transport material (HTM), the 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (spiro-OMeTAD, Lumtec) precursor was firstly prepared by dissolving 72.3 mg spiro-OMeTAD, 28.8 \\u03bcL 4-tert-butylpyridine (Sigma-Aldrich), and 17.5 \\u03bcL lithium bis(trifluoromethylsulphonyl)imide (Sigma-Aldrich) solution (520 mg mL\\u22121 in acetonitrile (Sigma-Aldrich)) and 8 \\u03bcL FK209-cobalt(III)-TFSI (Lumtec) solution (300 mg FK209-cobalt(III)-TFSI in 1 ml of acetonitrile) in 1 mL chlorobenzene (Sigma-Aldrich). The spiro-OMeTAD precursor was then deposited onto MAPbI3 by spin-coating at 3500 rpm for 30 s.\\nFor the front transparent electrode, 18 nm MoO3 (Sigma-Aldrich) was deposited on the spiro-OMeTAD by thermal evaporation at a rate of 0.7 \\u00c5 s\\u22121 under vacuum at 1 \\u00d7 10\\u22125 mTorr to protect the spiro-OMeTAD layer from sputtering damage during the deposition of indium tin oxide (ITO). The transparent contact was then fabricated by sputtering 100 nm ITO on the MoOx layer with 30 W RF power with Ar at 1.5 mTorr for 150 min using an AJA International sputtering system. A metal frame of silver was deposited by thermal evaporation to a thickness of 200 nm defining the active area of the cell. Finally, the front of the cell is covered by a textured polydimethylsiloxane (PDMS) foil for light trapping and antireflection (AR), see Fig. S8 (ESI\\u2020).\\n\\nThe depth dependent doping profiles of the p++ emitter of half silicon cells were measured using an electrochemical capacitance\\u2013voltage (ECV, CVP21, WEP) analyzer, calibrated using \\u03c1sh to account for the surface roughness.\\nX-ray photoelectron spectroscopy (XPS) was carried out using an ESCALAB250Xi, Thermo Scientific, UK.\\nThe current density\\u2013voltage (J\\u2013V) measurements of tandem devices were performed using a solar cell J\\u2013V testing system from Abet Technologies, Inc. (using a class AAA solar simulator) under an illumination power of 100 mW cm\\u22122 with a metal aperture (4 cm2 and 16 cm2) and a scan rate of 30 mV s\\u22121 in the direction from the open-circuit voltage (VOC) to the short-circuit current density (JSC) (1.8 V to \\u22120.1 V). The J\\u2013V curves of the best tandem devices were also measured with a forward scan at a scan rate of 30 mV s\\u22121 in the JSC to VOC direction (\\u22120.1 V to 1.8 V). The light was calibrated using a certified reference cell. The bias voltage for the steady-state measurements was chosen as the average of the maximum power point (MPP) voltage of the J\\u2013V measurement.\\nThe external quantum efficiency (EQE) measurement was carried out using the PV Measurement QXE7 Spectral Response system with monochromatic light from a xenon arc lamp. The EQE response was calibrated using two certified reference cells for the 300\\u20131000 nm and 1000\\u20131400 nm wavelength regions, respectively. A blue LED light (450 nm) and a near-infrared lamp were used to saturate the top and the bottom cell for the EQE measurement of the bottom silicon cell and the top perovskite cell, respectively.\\nThe steady state photoluminescence (PL) measurements were made with an Andor iVac CCD detector (the detector temperature is \\u221260 \\u00b0C). The excitation wavelength of the CW laser was 409 nm and the signal was collected using a 0.2 second exposure time.\\nTop view and cross-sectional scanning electron microscopy (SEM) images were obtained using a field emission SEM (NanoSEM 230). The optical reflection and transmission spectra were measured using a Perkin Elmer Lambda1050 UV/vis/NIR spectrophotometer. All measurements were undertaken at room temperature in ambient conditions.\\n\\nThe optical simulations of the perovskite/silicon tandem solar cell were performed using SunSolve\\u2122 ray tracing from PVLighthouse. Optically, silicon was treated to be bulk and non-coherent in the simulation. The simulation package does not allow for carrier recombination input. Therefore 100% internal quantum efficiency is assumed for both the top and bottom cells. The optical values (n, k) of SnO2, the perovskite, spiro-MeOTAD, MoO3 and ITO were all extracted from spectral ellipsometry measurements (JA Woollam Inc.) and fitted by WVASE\\u00ae software. Other optical values (n, k) of PDMS, Ag and NiOx are obtained from PVLighthouse.\\n\\nA commercial software package, Sentaurus technology computer-aided design (TCAD), was used to investigate the carrier transport mechanism between SnO2 and Si. The simulator solves Poisson, drift-diffusion and carrier conservation equations numerically until self-consistency is reached. The heterojunction was modelled with a similar approach to . For Si, state-of-the-art models highlighted by Altermatt and the latest Auger model were applied in the simulation to accurately predict silicon characteristics. For SnO2, the key material parameters are determined from various papers as listed in Table 1. Several essential models are employed to compute carrier transport including Fermi statistics, and Shockley\\u2013Reed\\u2013Hall models. Due to the bandgap discontinuity at the hetero-interface, the thermionic emission model is applied to compute the current density and energy flux density across the interface. With the presence of silicon oxide between SnO2 and Si, the tunnelling mechanism is enabled with the same approach delineated in .\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.159,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"TiS2 powder was synthesized by the chemical vapor transport method. To obtain 2D TiS2 nanosheets, 1.2 g of TiS2 powder was dispersed in 120 mL isopropanol alcohol (IPA) followed by sonication for 4 h at 600 W. The exfoliated 2D TiS2 suspension in IPA was centrifuged at speed of 8000 rpm for 30 min to separate nonexfoliated materials and thick 2D TiS2 flakes and the supernatant containing several layers of 2D TiS2 was used for preparing TiS2 films.\\n\\nThe planar PSCs were fabricated with a structure of FTO/ETL/perovskite/spiro-OMeTAD/Au. FTO based glass substrates were cleaned in an ultrasonic bath of water, acetone and isopropanol alcohol successively. The substrates were treated under UVO for 10 min to obtain hydrophilic surfaces. Then a 2D TiS2 suspension in IPA with different concentrations was spin-coated on the FTO substrates with different speeds. By contrast, a TiO2 film was prepared by the method reported in our previously published studies. The perovskite precursor solution containing PbI2 (99.99%, Alfa Aesar), CH3NH3I or HC(NH2)2I (Xi'an Polymer Light Technology Corp.) was dissolved in dimethyl sulfoxide (DMSO, 99.9%, Aldrich) and N,N-dimethylformamide (DMF, 99.8%, Alfa Aesar). The mixed solution was spin-coated on top of the ETLs (TiS2 or TiO2) at 1000 rpm for 5 s and 4000 rpm for 45 s while dripping chlorobenzene onto the substrate during the second spinning step. The samples were then heated at 100 \\u00b0C for 10 min (MAPbI3) or 150 \\u00b0C for 30 min (FA0.85MA0.15PbI3) resulting in the formation of dark perovskite films. Spiro-OMeTAD in chlorobenzene added with 4-tert-butylpyridine (TBP, Sigma Aldrich) and bis(trifluoromethylsulfonyl)imidelithium salt (Li-TFSI, Sigma Aldrich) was spin-coated as a hole transport layer on top of the perovskite films. Finally, an 80 nm-thick gold layer was thermally evaporated as the top electrode using a shadow mask to form an device active area of 9 mm2. For the flexible PSCs, PET/ITO was used to replace glass/FTO as the substrate, and the ETL, perovskite layer, spiro-OMeTAD and Au electrodes were prepared by the same process on a rigid glass substrate.\\n\\nTransmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM) and selected area electron diffraction (SAED) images were recorded with a JEM-2800 JEOL operated at 200 kV. EDS was performed on a TEM (JEM-2800 JEOL). SEM images of TiS2 nanosheets and the cross-sectional images of PSCs were obtained under a HITACHI, SU-8020 microscope. The transmittance spectrum of the TiS2 film was measured by using a UV/Vis NIR spectrophotometer (PerkinElmer, Lambda 950). The XRD spectrum was obtained using a D/MAX 2400 diffractometer with Cu K\\u03b1 radiation (Rigaku). Time resolved photoluminescence (TRPL) spectra were measured by using a PicoQuant FluoTime 300. The band structure of the TiS2 film was analysed using ultra-violet photoelectron spectra (UPS, ESCALAB 250Xi, Thermo Fisher). The J\\u2013V characteristics of the PSCs were collected using a SAN-EI ELECTRIC XES-40S2-CE solar simulator under a simulated sunlight intensity of 100 mW cm\\u22122. The solar simulator was calibrated with a standard silicon reference cell. The external quantum efficiency (EQE) of the PSC was determined by using a QTest Station 2000ADI system (Crowntech Inc.), including a tungsten\\u2013halogen lamp, a Si detector and a monochromator. The photoelectrochemical properties of TiO2 and TiS2 thin films were measured with a three-electrode configuration using a Ag/AgCl as the reference electrode, a Pt wire as the counter electrode and an aqueous solution of 0.5 mol L\\u22121 Na2SO4 as the electrolyte. Photoelectrochemical current density and time curves were measured under 365 nm UV light illumination with a light intensity of 100 mW cm\\u22122. For the UV-aging experiment, a UV light source (Kimmon laser, \\u03bb = 365 nm) with an intensity of 10 mW cm\\u22122 was used to irradiate the PSCs based on TiS2 and TiO2 ETLs.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiS2,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3PbI3 precursor solution is prepared by mixing an equimolar ratio of CH3NH3I (Dyesol) and PbI2 (ultra-dry 99.999% (metals basis), from Alfa Aesar) in N,N-dimethylformamide, and then heating at 60 \\u00b0C until complete dissolution of precursors. The solution is filtered through a 0.2 \\u03bcm GHP filter and the additive HI (57% in water, Aldrich) or NH4I (99% Aldrich) is added. The concentration of precursors is 40 wt% and 20 wt% for HI and NH4I respectively. Such concentrations have been selected in order to have similar film thicknesses with HI and NH4I. For optical characterization, we use a 25 mM and 150 \\u03bcM CH3NH3PbI3 precursor solution in DMF added with HI or NH4I. For morphological characterization, precursor solutions are prepared at the same concentration of solutions used for device fabrication.\\n\\nA ZetasizerNano ZS90 (Malvern, USA) equipped with a 4.0 mW He\\u2013Ne laser operating at 633 nm and an Avalanche photodiode detector was used. Measurements were performed in low-volume disposable cuvettes kept at 25 \\u00b0C. Typical concentrations: 1 wt% in DMF solvent.\\n\\nTo fabricate a device with the standard configuration, a 90 nm thick TiO2 compact layer is deposited on a cleaned FTO/glass substrates (Pilkington, TEC15) by spin-coating (3000 rpm) a double layer of 0.15 M and a final layer of 0.3 M titanium diisopropoxide bis(acetylacetonate) (75% Aldrich) in 1-butanol (Aldrich). Between each layer a mild annealing step (125 \\u00b0C for 5 min) is performed. Finally, the TiO2 coated FTO glasses are heated at 550 \\u00b0C for 2 hours. The CH3NH3PbI3 solution with additives is spin-coated at 4000 rpm for 200 s, in the case of HI, and at 7000 rpm for 30 s on a preheated (100 \\u00b0C) substrate for NH4I. The films are then annealed at 100 \\u00b0C for 2 min (HI) or 110 \\u00b0C for 100 min (NH4I). Then, a Spiro-OMeTAD/chlorobenzene solution (63 mg per 1 mL) added with 29 \\u03bcl tert-butylpyridine and 41 \\u03bcl lithium bis(trifluoromethylsulfonyl) imide salt/1-butanol (170 mg per 1 mL) is spin-coated at 2500 rpm for 30 s. Solar cell devices are completed by thermal evaporation of 100 nm Au electrodes.\\nFor the inverted device configuration a 40 nm poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT:PSS, Clevios P 4083, filtered through a 0,45 \\u03bcm PTFE filter) thick layer is spin-coated on a cleaned In-doped SnO2 (ITO) glass substrate (Visiontek) at 3000 rpm for 60 s and heated at 150 \\u00b0C for 15 min. Then, the CH3NH3PbI3 solution with additives are spin-casted and annealed following the same protocols described earlier. Finally, the PC61BM solution (25 mg ml\\u22121 in chlorobenzene) is deposited by spin coating at 1000 rpm for 30 s. LiF (0,6 nm) and Al (150 nm) electrodes are deposited by thermal evaporation. The current\\u2013voltage characteristics are determined using an Air Mass 1.5 global (AM 1.5 G) solar simulator (Spectra Physics Oriel150 W) with an irradiation intensity of 100 mW cm\\u22122 and recorded with a Keithley 2400 source meter. The step voltage is fixed at 10 mV and the delay time to 100 ms.\\n\\nThe absorption spectra of the CH3NH3PbI3 precursor solutions are recorded with a Varian Cary 5000 UV-vis-NIR spectrophotometer. For the UV-vis NIR measurement we use 1 mm length-path cuvettes.\\nScanning electron microscopy (SEM) imaging is performed by using a MERLIN Zeiss SEM FEG instrument at an accelerating voltage of 5 kV using an In-lens detector.\\nThe XRD spectra of the prepared films were recorded with a PANalytical X'Pert-PRO Materials Research Diffractometer using graphite-monochromated CuK\\u03b1 radiation (\\u03bb = 1.5405 \\u00c5).\\n\\nTime resolved photoluminescence measurements were performed using time-correlated single-photon counting (TCSPC) apparatus of Hamamatsu FL980, 100 ps time resolution with deconvolution analysis.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: HI,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Butylamine hydroiodide (BAI, 99%), guanidinium iodide (GAI, 99%), phenylethylammonium iodide (PEAI, 99%) and bathocuproine (BCP, 99%) were purchased from TCI. Methylammonium iodide (MAI, 99%) and methylammonium chloride (MACl, 99%) were purchased from Shanghai Mater Win New Materials. PbI2 (99%) and N,N-dimethylformamide (DMF, 99%) were purchased from Alfa Aesar. Formamide (99.5%), chloroform (CF, 99%) and ethyl alcohol (99%) were ordered from Sigma Aldrich. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) aqueous solution (Al 4083) was purchased from Baytron. (6,6)-Phenyl-C61-butyric acid methyl ester (PCBM, 99%) was purchased from American Dye Source. All reagents and solvents were used directly unless otherwise specified.\\n\\nThe ITO coated glass substrates were cleaned sequentially in detergent (Hellmanex III, 2 vol%), deionized water, acetone, and isopropanol in an ultrasonic bath for 15 min, respectively. After that, the substrates were dried in a nitrogen flow and cleaned by UV\\u2013ozone treatment for 20 min before use. A PEDOT:PSS HTL was prepared by spin coating at 4000 rpm for 40 s, followed by annealing at 140 \\u00b0C for 20 min. BAI, GAI (PEAI), MAI and PbI2 were mixed in a 1.8:0.2:4:5 molar ratio in DMF (with 3% formamide addition) with concentrations of 0.4 M, 0.6 M, and 0.8 M (based on PbI2). The optimized perovskite film with MACl addition was fabricated by mixing BAI, GAI, MAI, MACl and PbI2 in a molar ratio of 1.8:0.2:3.6:0.4:5 in DMF (with 3% formamide addition) with a concentration of 0.6 M (based on PbI2). The perovskite precursor solution and PEDOT:PSS substrates were heated to 70 \\u00b0C before spin coating of the perovskite layer. The spin-coating process started initially at 1000 rpm for 10 s and was then continued at 6000 rpm for 60 s after dropping the hot precursor onto the preheated PEDOT:PSS substrate, followed by annealing at 100 \\u00b0C for 10 min. PCBM (5 mg ml\\u22121 in CF) was spin-coated on the perovskite film at 2000 rpm for 30 s. BCP (0.5 mg ml\\u22121 in ethyl alcohol) was then spin-coated on PCBM at 3000 rpm for 30 s, followed by deposition of 100 nm Ag in a vacuum chamber under a high vacuum of 5 \\u00d7 10\\u22124 Pa. The device area is defined as 0.06 cm2 with a mask by measuring the intersection area between the mask and the ITO electrode.\\n\\nThe field-emission scanning electron microscope (FESEM) measurements were carried out on a Hitachi S-4800 machine. The crystallographic properties of the perovskite films were investigated using a Rigaku Ultima IV diffractometer with Cu K\\u03b1 radiation of 0.15406 nm (graphite mono-chromatic) at a scanning rate of 10\\u00b0 min\\u22121. GIWAXS measurements were carried out with a Xeuss 2.0 SAXS/WAXS laboratory beamline using a Cu X-ray source (8.05 keV, 1.54 \\u00c5) and a Pilatus3R 300K detector. The incidence angle is 0.3\\u00b0. The UV-visible absorption spectra were recorded on a UV-2450 UV-vis Shimadzu Spectrophotometer. The steady-state PL was measured on an FLSP920 from Edinburgh Instruments, and excitation was provided by a xenon lamp at 470 nm.\\nThe time-of-flight secondary-ion mass spectrometry (TOF-SIMS) spectra were recorded on a TOF-SIMS V instrument (Ion-TOF, GmbH, Germany) to track the depth distributions of GA+, PEA+ and In3+ from the top of the perovskite film down to the ITO substrate. Dual beam depth profiling used a pulsed 30 keV Bi3++ liquid metal ion gun as a primary ion source and a 10 keV argon gas cluster ion beam with the beam current being lowered to 1 nA as a sputtering ion source in an interlaced mode. At first, the sputter beam was used to sputter the sample surface for 20 s (or 30 s) to clean possible contamination on the sample surface during sample preparation. Then, data were collected until we reached the ITO layer as indicated by the sharp increase in the In+ ion or the InO\\u2212 ion intensity. The analysis area was 100 \\u00d7 100 \\u03bcm2 in the center of a crater of 300 \\u00d7 300 \\u03bcm2. A low energy flood gun was used for charge compensation during analysis. Positive ion spectra were obtained in a high current bunched mode and mass calibrated using GA+, PEA+ and In3+. Negative ion spectra were obtained in a high current bunched mode and mass calibrated using Cl\\u2212 and InO\\u2212. The amount and distribution of GA+ (PEA+) inside the perovskite layer can be illustrated by the relative intensity of GA+ (PEA+), until the enhancement of the relative intensity of the In3+ signal. All geometries of intermediates were optimized under tight criteria using the BHandH/6-31G(d,p) method. Frequency calculations confirmed that the intermediates in the ground state had zero imaginary frequency. All calculations were performed using Gaussian 16 program software.\\nThe photocurrent density\\u2013voltage (J\\u2013V) measurement was performed using a solar simulator (SS-F5-3A, Enlitech) along with an AM 1.5G spectrum whose intensity was calibrated using a certified standard silicon solar cell (SRC-2020, Enlitech) at 100 mV cm\\u22122. J\\u2013V curves of the unsealed PVSCs were measured with a mask. The forward scan voltage is from \\u22120.1 V to 1.2 V, and the reverse scan voltage is from 1.2 V to \\u22120.1 V. The scan speed is 0.1 V s\\u22121, the dwell time is 1 ms, and the voltage step is 0.02 V for both scan directions. The measurement is performed at room temperature in a glovebox without aging of the devices. The average PCE is calculated based on 30 devices. The external quantum efficiency (EQE) data were obtained by using a solar-cell spectral-response measurement system (QE-R, Enlitech). The perovskite solar cells were kept in a humidity-controlled cabinet (Hr = 50 \\u00b1 5% or 25 \\u00b1 5%; Bossmen, PR1852(A)-SH) for humidity-stability measurement.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: BA2MA4Pb5I16,\\n Perovskite_composition_short_form: BAMAPbI,\\n Perovskite_additives_compounds: Formamide; Guadinium,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Isopropanol (IPA, anhydrous, 99.5%), methylamine (\\u226598%), HI (99.95%, 57 wt% solution in water), 4-tert-butylpyridine (96%), lithium bistrifluoromethanesulfonimidate (LiTFSI, 99.95%), PbI2 (99.999%), N,N-dimethylformamide (DMF, anhydrous, 99.8%), and poly(3-hexylthiophene) (P3HT, Mn 54000\\u201375000), titanium diisopropoxide bis(acetylacetonate) (TDB, 75 wt% in IPA) were all purchased from Aldrich and used as received. Dyesol 18NRT titania paste (TiO2) and 2,2\\u2032,7,7\\u2032-tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9\\u2032-spirobifluorene (spiro-MeOTAD, Fenglin Chemicals, 99.5%) were also used as received.\\n\\nMAI was synthesized according to the method reported elsewhere. This involved the dropwise addition of 30 mL of aqueous HI solution (57 wt%) to 27.9 mL of an aqueous solution of methylamine (40 wt%) in an ice bath with stirring. The cold solution was stirred for 2 h, and the solvent was evaporated using a rotary evaporator. The crystals were washed using diethyl ether three times and dried in a vacuum oven. ITO/glass slides (2.0 cm \\u00d7 1.5 cm) were cleaned by sonication in a 1% Hellmanex solution in boiling water for 15 min followed by rinsing with water and IPA and cleaning in ultrasonic for 5 min and dried using a nitrogen stream. Titania paste (70 \\u03bcL, 1:5 in ethanol) was spin-coated onto the cleaned glass slides at 5000 rpm for 30 s to form a mesoporous scaffold (mp-TiO2) with an average thickness of 250 nm. The films were then annealed at 500 \\u00b0C for 30 min. Next, solutions of PbI2 + xMAI in DMF containing PbI2 (1.0 M) and x = 0, 0.33, 0.50, 0.66, 1.00 M of MAI were prepared in a glove box (humidity \\u223c2%). Film fabrication was subsequently conducted outside of the glove box (humidity \\u223c40%). The solutions were spin-coated onto the mp-TiO2 layer (Scheme 1). Note that x = 0 and 1.0 correspond to the 2-s and 1-s methods, respectively. The values x = 0.33, 0.50 and 0.66 correspond to 1 & 2-s films. The solutions were kept at 70 \\u00b0C during spin-coating. The spin-coating conditions employed were 2000 rpm for 40 s for the 1-s and 1 & 2-s methods; whereas, 6500 rpm for 60 s was used for the 2-s method. The films were dried at 100 \\u00b0C for 15 min (or 30 min for 1-s, x = 1.0). The dried films (with the exception of the 1-s film) were washed with IPA for 3 s and then dipped in 20 mL MAI (10 mg mL\\u22121) for 15 min. The films were dried at 100 \\u00b0C for 15 min and immediately placed in a desiccator over P2O5 and stored in the dark until investigation. The 1s and 1 & 2-s film layer thicknesses were in the range 550\\u2013700 nm. The thickness for the x = 0 film was 350 nm.\\n\\nLaser-patterned, ITO-coated glass substrates (20 \\u03a9 sq\\u22121) were cleaned by ultrasonication in a 2% Hellmanex solution, rinsed with deionized water and IPA, and dried. A blocking layer of compact TiO2 (bl-TiO2) was then deposited by spin coating TDB (75 \\u03bcL, 0.15 M) solution in 1-butanol at 2000 rpm for 60 s. The procedure was repeated using a TDB solution (0.30 M) and the substrate was heated at 125 \\u00b0C for 5 min to give an average thickness of 50 nm. A mp-TiO2 layer was then deposited as described above. Perovskite photoactive layers were then deposited as described above. P3HT was deposited as a hole transport matrix (HTM). The latter (average thickness of 100 nm) was deposited by dynamic spincoating of P3HT in toluene (15 mg mL\\u22121) at 4000 rpm for 20 s. Following Heo et al., Li-TFSI salt and t-BP in acetonitrile were added to the P3HT solution. Finally, a gold layer (70 nm) was deposited on top of the HTM. The fabrication procedures were performed outside the glovebox in \\u223c40% relative humidity. Devices were also prepared using spiro-MeOTAD as the HTM with an average thickness of 100 nm. In that case HTM deposition followed established literature procedures. All devices were stored in a desiccator over P2O5 in the dark until investigation.\\n\\nThe surface morphologies were investigated using a Philips XL30 FEI-SEM. The device cross section was prepared with Ar ion polishing at 6 kV and cleaned at 1 kV using Ilion system from Gatan (France). The cross-section microstructure was investigated using a FEI Magellan FEG-SEM and the local composition probed via energy dispersive X-ray spectroscopy (EDX). XRD data were obtained using a Bruker D8 Advance diffractometer (Cu-K\\u03b1). The films obtained were scanned between 10 and 50\\u00b0 with a step size of 0.02. For these measurements the films were prepared and measured under a nitrogen atmosphere. UV-visible spectra were recorded using a Perkin Elmer Lambda 25 spectrometer. Optical images were obtained using an Olympus BX41 polarizing microscope with an Olympus U-AN360-3 rotatable analyser and polariser filter. PL spectra were obtained using an Edinburgh Instruments FLS980 spectrometer. Pump\\u2013probe microsecond to millisecond transient absorption spectroscopy (TAS) measurements were conducted on mp-TiO2/MAPbI3/spiro-MeOTAD films excited by a dye laser (Photon Technology International GL-301, sub-nanosecond pulse width) pumped by a pulsed nitrogen laser (Photon Technology International GL-3300). A quartz halogen lamp (Bentham IL1) was passed through a monochromator and used to probe changes in the absorption characteristics of the films as a function of time after the laser excitation. The probe light was detected using home-built silicon (\\u22641000 nm) or InxGa1\\u2212xAs (>1000 nm) photodiodes and an oscilloscope. Perovskite films were kept under flowing N2 during the measurements. All TAS measurements employed 567 nm laser pulses (25 \\u03bcJ cm\\u22122).\\n\\nThe current density\\u2013voltage (J\\u2013V) characteristics were measured using a Keithley 2420 Sourcemeter and 100 mW cm\\u22122 illumination (AM 1.5G) and a calibrated NREL certified Oriel Si-reference cell. An Oriel SOL3A solar simulator was used for these experiments. The active area of the devices was defined using a square aperture within a mask and fixed at 0.16 cm2. Forward and reverse direction sweeps were measured with a sweep rate of 100 mV s\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 15.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I was synthesized using the method reported in . Briefly, 30 ml of methylamine (40% in methanol) was mixed with 32.3 ml of hydroiodic acid (57 wt% in water) in a round-bottom flask at 0 \\u00b0C for 2 h with stirring. The solvent was removed by heating the solution in a rotary evaporator at 50 \\u00b0C for 30 min. The white-yellow precipitates of raw CH3NH3I were washed with ethanol, filtered and then washed with diethyl ether again. This procedure was repeated three times. After the last filtration, the products were dried at 70 \\u00b0C in a vacuum oven for 8 h.\\n\\nThe devices were prepared on cleaned fluorine-doped tin oxide (FTO) substrates. FTO glass (20 \\u03a9 \\u25a1\\u22121) was first etched to form a strip of conductive area on the edge side by HCl and Zn powders. The etched substrates were then sequentially cleaned in soap water, acetone, deionized water, and ethanol in an ultrasonic bath, and then dried under nitrogen flow, followed by putting the cleaned FTO in a 0.2 M TiCl4 solution at 70 \\u00b0C for one hour to prepare the compact TiO2 (c-TiO2) blocking layer. For interface modification, a dual-electron transporting layer was introduced, phenyl-C61-butyric acid methyl ester (PCBM, a fullerene derivative) dissolved in chlorobenzene with 20 mg ml\\u22121 was deposited on the compact TiO2 layer by spin-coating at 3000 rpm, which provided a uniform PCBM film of 15 nm. The PCBM/TiO2 coated substrates were put onto a hot plate and covered by a glass Petri dish. 15 \\u03bcl of the CB solvent was added at the edge of the Petri dish during the thermal annealing at a temperature of 100 \\u00b0C for 30 min. Then, the PbI2 film with a thickness of about 150 nm was deposited by vacuum thermal evaporation at an evaporation rate of 0.5 \\u00c5 s\\u22121 monitored by a quartz microbalance sensor. The as-grown PbI2 films were fixed onto quadrate Al2O3 boat covers and the PbI2-coated substrates were about 2 cm above the CH3NH3I powders with the PbI2 side facing downward. Then, this boat was moved into a quartz tube furnace with the temperature controlled at 110 \\u00b0C, 120 \\u00b0C, 130 \\u00b0C, and 140 \\u00b0C, respectively, for an hour in air to grow the perovskite film, and the environmental humidity was controlled under 25%. Finally, possible redundant MAI powder was washed with isopropanol (IPA) and the as-grown samples were ready for characterization. The hole transporting layer was deposited by spin-coating a solution at 3000 rpm for 30 s composed of 72.3 mg Spiro-OMeTAD (Ningbo Borun), 28.8 \\u03bcl of 4-tert-butylpyridine, and 17.5 \\u03bcl of lithium-bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg in 1 ml of acetonitrile, all dissolved in 1 ml of chlorobenzene). Silver (Ag, 120 nm) back contacts were thermally evaporated onto the Spiro-OMeTAD layer at 1 \\u00d7 10\\u22126 Torr in a vacuum deposition chamber. The flexible devices were fabricated on an indium-doped tin oxide (ITO)/polyethylene terephthalate (PET) substrate. The PEDOT:PSS layer was casted on the top of ITO at 5000 rpm for 30 s. Then the substrates were annealed at 120 \\u00b0C for 15 min, and the perovskite film was synthesized as above. The PCBM layer was spin-coated at 5000 rpm for 30 s from chlorobenzene with a concentration of 20 mg ml\\u22121. At last, silver (Ag, 120 nm) back contacts were thermally evaporated on the PCBM film at 1 \\u00d7 10\\u22126 Torr in a vacuum deposition chamber.\\n\\nPerovskite CH3NH3PbI3 thin films for scanning electron microscopy (SEM), X-ray diffraction (XRD), optical absorption and steady photoluminescence measurements were prepared using the same growth conditions as for the solar cells. The SEM images were obtained using a Quanta FEG250 field emission scanning electron microscope. An X-ray diffractometer (D8-Advance, Bruker) was employed to characterize the crystalline properties of the CH3NH3PbI3 films. The UV-visible (UV-Vis) optical absorption spectrum was measured with a Shimadzu UV-3600 spectrophotometer. Steady photoluminescence was excited with a 450 nm diode laser source. The solar cell current density versus voltage (J\\u2013V) characteristics were measured using a Keithley Source Meter 2612A in the dark or under AM 1.5G simulated solar illumination with an intensity of 100 mW cm\\u22122 (San-Ei, calibrated by a NREL-traceable KG5 filtered silicon reference cell) with different scanning directions. The metal cathodes were measured with a mask and the device area was determined by the overlap of the metal electrodes. Accurate device areas (0.1 cm2) were measured device-by-device using a calibrated optical microscope. The incident-photon-to-current conversion efficiency (IPCE) was measured with a QEX10 photoresponse system (PV Measurement Inc.).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: CBD | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: none >> none,\\n Perovskite_deposition_procedure: Evaporation >> Gas reaction,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 110.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead acetate trihydrate (Pb(Ac)2\\u00b73H2O, 99.95%), methylamine iodide (MAI, 99.5%), 2,2\\u2032,7,7\\u2032-tetrakis(N,N\\u2032-di-methoxyphenylamine)-9,9\\u2032-spirobifluorene (spiro-OMeTAD, 99.5%), lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI, 99.9%) and 4-tert butylpyridine (tbp, 96%) were purchased from Xi'an Polymer Light Technology Corp. N,N-Dimethylformamide (DMF, 99.9%) and chlorobenzene (CB, 99.9%) were purchased from Sigma-Aldrich. Isopropyl alcohol (IPA, 99.8%) and ethanol (99.5%) were purchased from Aldrich. Fluorine-doped tin oxide (FTO)-coated glass substrates (15 \\u03a9 sq\\u22121) were bought from OPV Tech New Energy Co.\\nIn detail, 1 mmol of Pb(Ac)2\\u00b73H2O was mixed with 3 mmol of MAI in 1 mL of anhydrous DMF, and the mixture was stirred overnight at room temperature.\\n\\nPlanar PSCs were fabricated on FTO-coated glass substrates. The FTO substrates were ultrasonically cleaned with detergent, acetone, deionized water, and ethanol for 15 min. Then, the conductive substrates were dried with a nitrogen stream and treated with UV-ozone for 15 min. The device has the definite structure of FTO/c-TiO2/MAPbI3/spiro-OMeTAD/Ag. A compact layer of TiO2 was spin-coated on top of the FTO glass at 2000 rpm for 50 s, then moved onto a hot plate and maintained at 150 \\u00b0C; it was then sintered at 500 \\u00b0C in a muffle furnace for 30 min, followed by treatment with the TiCl4 solution at 70 \\u00b0C for 30 min to ensure reduction in the number of remaining pinholes. For the prepared perovskite film, the perovskite precursor solution was spin-coated onto the substrate at 4000 rpm for 55 s and then subjected to thermal annealing or solvent vapor annealing at 100 \\u00b0C. For the solvent vapor annealing film, the perovskite films were placed on top of a hot plate and covered by a glass Petri dish. DMF in different volumes (0 \\u03bcL, 5 \\u03bcL, 10 \\u03bcL, 15 \\u03bcL, 20 \\u03bcL, and 25 \\u03bcL) was added around the substrates during the formation of perovskite films. The processing scheme for the formation of the perovskite film using the solvent-vapor annealing method is shown in Fig. 1. After this, a layer of hole transport material (72.3 mg of spiro-OMeTAD, 17.5 \\u03bcL of Li-TFSI solution (520 mg of Li-TFSI in 1 mL of acetonitrile) and 28.8 \\u03bcL of tBP were dissolved in 1 mL of CB) was spin-coated on the perovskite active layer at 4000 rpm for 20 s to form the hole transport layer. Finally, a metallic silver electrode was deposited by the magnetron sputtering technique.\\n\\nThe morphology of the perovskite film was characterized using scanning electron microscopy (SEM, ZEISS EV0MA15). The crystal structure of the perovskite film was characterized by X-ray diffraction (XRD, DX-2700, Dandong) with Cu K\\u03b1 radiation (\\u03bb = 0.15406 nm) at the scanning rate of 5\\u00b0 min\\u22121. The absorption spectrum of the perovskite film was obtained using a UV\\u2013vis spectrometer (UV-2600, SHIMADZU). The steady-state and time-resolved photoluminescence spectroscopy were performed at 475 nm upon excitation at 450 nm at the pulse frequency of 1 MHz (FLS980, Edinburgh). The photocurrent\\u2013voltage characteristics of perovskite solar cells were determined using an electrochemical workstation (CHI660D, Chenhua) under AM 1.5 simulated illumination (CEL-S500, Beijing, China). The monochromatic incident photon-to-current conversion efficiency (IPCE) was determined using an IPCE system (PVE 300, Bentham, Inc.) in the wavelength range of 300\\u2013800 nm. Moreover, using a mask, the active area of the solar cells was controlled at 0.12 cm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine-doped tin oxide (FTO) glass substrates with a sheet resistance of 14 \\u03a9 sq\\u22121 were supplied from Asahi Glass (Japan). Methylammonium bromide (MABr) and formamidinium iodide (FAI) were purchased from Dyesol. Lead(II) bromide (PbBr2, 99.99%), cesium iodide (CsI, 99.99%), bis(trifluoromethane)sulfonimide lithium salt (Li-TFSI, 99%), poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) and 4-tert-butylpyridine (TBP, 96%) were purchased from Xi'an Polymer Light Technology Corp. Tin(II) chloride dehydrate (SnCl2\\u00b72H2O), thiourea, dimethyl sulfoxide (DMSO), N,N-dimethylformamide (DMF), acetonitrile, K chunks (99.99%), rubrene powder (sublimed grade, 99.9%) and chlorobenzene (CB) were purchased from Sigma-Aldrich. Lead(II) iodide (PbI2, 99.8%) was purchased from TCI while spiro-MeOTAD [2,2,7,7-tetrakis(N,N-di-p-methoxyphenyl-amine)-9,9-spirobifluorene] (99.5%) was purchased from Feiming Science and Technology Co., Ltd Luminescence Technology Corp. All chemicals were used as received.\\n\\nK chunks and rubrene powder were stored and handled in an argon-filled glove box (O2 and H2O < 1 ppm), then transferred to a Pyrex ampoule at a molar ratio of 2:1. After being sealed under vacuum (<10\\u22124 mbar), reactions were performed at 210 \\u00b0C with a heating rate of 1\\u00b0C min\\u22121 and a dwelling time of 3 days. The products were then reground and re-pelletized for another 3 day reaction at the same temperatures to yield the final product K2Rubrene.\\nThe PSCs were prepared on FTO substrates which were cleaned in detergent and then successively sonicated in deionized water, acetone, and isopropyl alcohol solution, and then dried in an oven at 80 \\u00b0C. Prior to the deposition of electron transport layers (ETLs), FTO substrates were exposed to UV\\u2013ozone for 20 min. A SnO2 quantum dots (QDs) film was prepared according to the report of Fang et al. Perovskite photoactive layers were deposited on the ETLs by an anti-solvent method, as described in the literature. The (CsI)0.04(FAI)0.82(PbI2)0.86(MAPbBr3)0.14 and MAPbI3 precursor solutions were prepared in a glove box from 1.35 M Pb2+ in a mixed solvent of DMF and DMSO (4:1 v/v). The dissolved solution was then spin-coated on the FTO/SnO2 QD ETLs substrate at 4500 rpm for 30 s in a glove box; note that 150 \\u03bcL K2Rubrene and rubrene chlorobenzene solution of 1 mM concentrations were pipetted onto the spinning film 15 s before the end of this program. Thereafter, the as-cast perovskite films were annealed at 150 \\u00b0C for 10 minutes. After cooling down to room temperature, spiro-OMeTAD solution (75 mg dissolved in 1 mL chlorobenzene) with 29 \\u03bcL of TBP and 17.5 \\u03bcL of Li-TFSI (520 mg mL\\u22121 in acetonitrile) was spin-coated on the perovskite layer at 4000 rpm for 20 s in a glove box. Finally, gold was deposited by thermal evaporation on top of the spiro-OMeTAD layer to complete the device, using a shadow mask to pattern the electrodes. The active area of the cells was 0.09 cm2, which was defined by the area of the Au electrode.\\n\\nThe J\\u2013V characteristics of the devices were measured using a B1500 A semiconductor parameter analyzer under an AAA class ORIEL Sol3A solar simulator equipped with an AM 1.5 filter, the light intensity was set at 100 mW cm\\u22122 using a calibrated standard monocrystalline Si reference cell from Newport traceable to NREL. The hole-only devices with the FTO/PEDOT:PSS/K2Rubrene (or rubrene)/Au structure were measured under dark ambient conditions. Scanning was carried out at a scan rate of 0.1 V s\\u22121. The scans started and finished under forward bias and had 2 seconds stabilization time at forward bias under illumination prior to scanning. The corresponding incident photon-to-current efficiency (IPCE) spectrum was measured in air by a QE-R 3011 system from Enli Technology Co. Ltd. (Enli).\\nUV-visible spectroscopy was performed using a UV-VIS-NIR spectrophotometer (UV-2550 Shimadzu) in the 200\\u2013800 nm wavelength range at room temperature. Fourier transform infra-red (FTIR) spectra were recorded with a reflectance (ATR) instrument (PerkinElmer Spectrum 100, USA) from 4000 to 800 cm\\u22121 with a resolution of 2 cm\\u22121. X-ray diffraction (XRD) patterns were determined using a Rigaku SmartLab X-ray diffractometer with Cu K\\u03b1 radiation. The morphologies of PSCs were investigated by a high-resolution field emission scanning electron microscope (SEM, JSM7100F). Based on the tapping mode atomic force microscopy (AFM, Bruker NanoScope MultiMode 8) system, electrostatic force microscopy (EFM) simultaneously measures contact potential difference (CPD) between the probe (Nanosensor PPP-EFM) and the surface of a perovskite sample by constantly probing. For our EFM measurements, a two-pass technique with phase mode was employed. The first pass was used to acquire the topographic height, and then the conductive probe was lifted with respect to the specimen surface with a constant separation, approximately 10 nm here, and scanned to acquire the potential offset between the tip and the sample. The first resonant oscillation of the cantilever (52.590 kHz) was used for the non-contact AFM topographic imaging. The second resonant frequency (60 kHz) was used for the potential imaging. We chose a scan rate of 0.977 Hz and a DC bias of 1 V applied to the conductive probe. The sample was fixed in a custom-made vertical sample holder with electrical connections to both electrodes. For photothermal deflection spectroscopy (PDS) measurements, the perovskite film was deposited on quartz substrate and then immersed into FC-72. A monochromatic light beam was modulated at 13 Hz by a mechanical chopper and was shone onto the sample. A laser was at the perpendicular side so that it was deflected periodically. A position detector, connected with a lock-in amplifier, was placed on the other side so that the deflection signal was measured. The photoluminescence (PL) spectrum and time-resolved photoluminescence (TRPL) signals of perovskite film were recorded using the Edinburgh FLSP920 spectrophotometer equipped with a 485 nm picosecond pulsed diode laser as the excitation source.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-QDs,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.04FA0.82MA0.14PbBr0.42I2.58,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless stated otherwise, all chemicals were used as received.\\nPreparation of the La\\u2013BaSnO3 nanoparticles and paste. La(NO3)3\\u00b76H2O (0.5 mmol), Ba(NO3)2 (9.5 mmol; 99%, Aldrich), and SnCl4\\u00b75H2O (10 mmol; 98%, Aldrich) were dissolved in an aqueous solution of hydrogen peroxide (170 mL; 30%, SCR) under constant stirring. After it became transparent, citric acid (5 mmol; J&K Scientific) was added to the mixture solution. Then, aqueous NH3\\u00b7H2O (120 mL; SCR) was introduced and the solution immediately became turbid with white precipitates. The turbid solution was stirred overnight at room temperature. The white precipitates were washed with distilled water and absolute ethanol, and then freeze-dried. After this, the dried precursor was calcined at 900 \\u00b0C for 2 h in air and finally grey powder of La-BaSnO3 was obtained.\\nThe La-BaSnO3 paste was homemade. Abovementioned La-BaSnO3 nanoparticles (1 g) were mixed with about 40 mL of absolute ethanol under alternate magnetic stirring and ultrasonication for 1 day. After this, 3.5 g of terpineol, 3 g of ethyl cellulose, and 0.3 g of acetylacetone were added to the suspension and mixed via alternate magnetic stirring and ultrasonication for 1 day. The resulting mixture was introduced into a rotary evaporator to remove excess ethanol. Finally, the paste was further treated with a three-roll mill.\\n\\nFTO glass (Pilkington TEC 15) 15 \\u03a9 \\u25a1\\u22121 was patterned by etching with Zn powder and 1 M aqueous HCl. Then, it was cleaned in an ultrasonic bath containing ethanol for 20 min, deionized water for 30 min, and treated at 510 \\u00b0C for 30 min. The dense blocking layer of TiO2 was deposited on the FTO substrate by aerosol spray pyrolysis at 450 \\u00b0C using a precursor solution of 0.4 mL of bis(acetylacetonate) and 0.6 mL of titanium diisopropoxide in 7 mL of isopropanol. The LBSO, BSO, and TiO2 (Dyesol 30NRT) paste were diluted in ethanol by a quality ratio of 1:5, 1:5, and 1:5.5, respectively. After the FTO substrate was cooled down to room temperature, mp-LBSO, mp-BSO, and mp-TiO2 were deposited by spin-coating their respective diluted paste (40 \\u03bcl) at 4000 r.p.m. for 30 s, and then annealed at 510 \\u00b0C for 30 min. A one-step spin-coating procedure was utilized to prepare the MAPbI3 layer. MAPbI3 precursor solution (1 M) was prepared by dissolving 462 mg of PbI2 (99%, Aldrich) and 159 mg of MAI in a mixture solvent of 0.15 mL of N,N-dimethylformamide (DMF, 99.8%, Sigma-Aldrich) and 0.85 mL of dimethyl sulfoxide (DMSO, 99.9%, Sigma-Aldrich) under stirring at 60 \\u00b0C. MAPbI3 precursor solution (30 \\u03bcl) was spin-coated on the mesoporous oxide film by a consecutive two-step spin-coating process at 1500 r.p.m. and 4500 r.p.m for 20 s and 30 s, respectively. During the second spin-coating step in the last 10 s, the substrate was treated with chlorobenzene. Subsequently, the film was annealed at 100 \\u00b0C for 60 min. A volume of spiro-OMeTAD (2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene, 30 \\u03bcl) solution was spin-coated on the perovskite layer at 3000 r.p.m. for 30 s. The solution was prepared by mixing 72.3 mg of spiro-OMeTAD, 28.8 \\u03bcl of TBP (4-tert-butylpyridine), 17.5 \\u03bcl of LiTFSI (lithium bis(trifluoromethylsulphonyl)imide, 520 mg in 1 mL of acetonitrile), and 29 \\u03bcl of FK209 (tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) bis(trifluoromethylsulphonyl)imide, 300 mg in 1 mL of acetonitrile). Finally, the back contact was made by thermally evaporating 60 nm gold on the top of the device.\\n\\nThe morphologies of all samples were characterized by a field-emission scanning electron microscope (FE-SEM, sirion200, FEI Corp., Holland). The XRD patterns were obtained using a Bruker-AXS Microdiffractometer (model D5005) with Cu K\\u03b1 radiation (\\u03bb = 1.5406 \\u00c5). UV-vis absorption spectra and transmittance spectrum were obtained using the UV-vis spectrophotometer (SOLID3700, Shimadzu Co. Ltd, Japan). The carrier mobilities of the mp-LBSO and mp-TiO2 films were measured by the steady-state DC current\\u2013voltage analysis using a computer controlled potentiostat (Autolab 320, Metrohm, Switzer land). The PL spectra were obtained by exciting the perovskite films deposited on glass at 473 nm with a standard 450 W xenon CW lamp. The signals were obtained by a spectrofluorometer (photon technology international) and analyzed by the software Fluorescence. Transient absorption (TA) responses of perovskites deposited on glass were obtained using LKS (LKS80, England). The samples were investigated using a pump light wavelength of 470 nm and a probe light wavelength of 775 nm. The repetition rate was 5 Hz, and the energy of the laser device was 150 \\u03bcJ cm\\u22122.\\nThe J\\u2013V curves were acquired using a Keithley model 2420 digital source meter controlled by Test point software under a xenon lamp (100 mW cm\\u22122). The IPCE values were confirmed as a function of wavelength from 300 to 900 nm (PV Measurements, Inc.). The irradiance was calibrated using a Si-reference cell certified by NREL. Current\\u2013voltage curves were obtained using a sourcemeter (Keithley 2400, USA). All solar cells were covered with a black mask, which was used to define the active area of the devices, and in this case, it was 0.09 cm2. The incident monochromatic photon-to-current conversion efficiency (IPCE) was measured using an IPCE measuring system (Newport Corporation, CA) equipped with a Xe lamp as the light source.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | BaSnO3-mp,\\n ETL_additives_compounds: Unknown | La,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO (fluorine-doped tin oxide) glasses (Pilkington, TEC-8, 8 \\u03a9 sq\\u22121) were cleaned with detergent and sonicated with ethanol for 15 min prior to coating with ETLs. For the c-TiO2 ETL, a precursor solution of 0.15 M titanium diisopropoxidebis(acetylacetonate) (75 wt% in 2-propanol, Aldrich) in 1-butanol (99.8%, Aldrich) was spin-coated at 700 rpm for 8 s, 1000 rpm for 10 s, and 2000 rpm for 40 s with an acceleration of 1200 rpm s\\u22121 to reach the speed set point, followed by annealing at 125 \\u00b0C for 10 min. This coating process was repeated three times. Finally, the film was annealed at 550 \\u00b0C for 60 min in air. The annealed c-TiO2 film was immersed in 10 mM aqueous TiCl4 (Sigma Aldrich, >98%) at 70 \\u00b0C for 20 min, rinsed with deionized water several times and then annealed again at 500 \\u00b0C for 60 min in air. For the PCBM overlayer on c-TiO2 or the PCBM layer as an ETL, a PCBM solution (20 mg ml\\u22121 in chlorobenzene) was spin-coated at 1200 rpm for 60 s with an acceleration of 1000 rpm s\\u22121 and then dried at room temperature for 20 min. In order to control the MAPbI3 (MA = methylammonium) perovskite film thickness, concentrations of the perovskite precursor solution were changed. The stock solution with a concentration of 2.71 M was prepared by dissolving CH3NH3I (0.159 g), PbI2 (0.461 g) and DMSO (71 \\u03bcl) in 0.369 ml of DMF, which was diluted to 2.37 M, 1.58 M and 0.95 M to decrease the perovskite film thickness. The precursor solution was filtered with a 0.45 \\u03bcm pore-sized filter, and was spin-coated on the ETL-coated substrate at 5000 rpm for 25 s with an acceleration of 1200 rpm s\\u22121. While spinning, 0.8 ml of diethyl ether was added dropwise at 10 s or 7 s after spinning for high concentration or low concentration perovskite precursor solutions, respectively. The perovskite film was heated at 65 \\u00b0C for 1 min and then at 100 \\u00b0C for 9 min. For deposition of the spiro-MeOTAD (2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene) layer, a coating solution was prepared by dissolving 72.3 mg of spiro-MeOTAD, 17.5 \\u03bcl of Li-TFSI (520 mg ml\\u22121 in acetonitrile) and 28.8 \\u03bcl of 4-tert-butylpyridine (tBP) in 1 ml chlorobenzene, and was spin-coated at 3000 rpm for 25 s. Finally, a Au electrode was deposited using a thermal evaporator.\\n\\nPhotocurrent density (J)\\u2013voltage (V) curves were measured with a solar simulator (Oriel Sol 3A, class AAA) equipped with a 450 W xenon lamp (Newport 6279NS) and a Keithley 2400 source meter. The light intensity was adjusted using a NREL-calibrated Si solar cell with a KG-5 filter. The active area was covered with a metal mask with a dimension of 0.125 cm2 during the measurement. The external quantum efficiency (EQE) was measured using an EQE system (PV measurement Inc.), where a monochromatic beam was generated from a 75 W xenon source lamp (USHIO, Japan) and data were collected in DC mode without bias light. The thickness of the perovskite layer was determined by using a scanning electron microscope (SEM, JSM7000F, JEOL). Impedance spectroscopy (IS) and admittance spectroscopy (AS) were performed with a PGSTAT 128N (Autolab, Eco-Chemie). IS was performed under illumination of 80 mW cm\\u22122 and in the dark at DC bias voltages ranging from 0 V to 1.0 V and a potential step of 0.1 V. The frequency range was between 1 MHz and 100 mHz. AS was performed under darkness and an AC sinusoidal signal of 20 mV was applied in the frequency range from 1 MHz to 100 mHz under open circuit conditions. Capacitance\\u2013voltage (C\\u2013V) curves were measured from a 1.5 V positive potential, where built-in potential was calculated at 2 kHz in the central plateau region.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65; 100,\\n Perovskite_deposition_thermal_annealing_time: 1.0; 9.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.125,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The MAPbI3\\u2212xClx perovskite precursor was synthesized according to the literature. One equivalent of hydroiodic acid (57 wt% in water, Aldrich) and 4 equivalents of methylamine (33 wt% in absolute ethanol, Aldrich) were stirred at 0 \\u00b0C for 2 h. The solvent was removed under reduced pressure. The product MAI was then recrystallized by dissolving it in ethanol and precipitating in diethyl ether for three times, and then dried at 50 \\u00b0C in a vacuum for 24 h. MAI and PbCl2 (99.999%, Alfa Aesar) were mixed in a molar ratio of 3:1 in anhydrous DMF (99.8%, Acros). The final concentration of the perovskite was controlled to ca. 40 wt%. After the reactants were dissolved, 1% 1,8-diiodooctane (DIO, a volume fraction of DMF) was added to the solution. The mixture was stirred overnight at 60 \\u00b0C under an N2 atmosphere. The solution with the perovskite precursor was stored in a glovebox, and filtrated with 0.45 \\u03bcm PTFE filters before use.\\n\\nPlanar p-i-n pero-SCs with the device configuration of ITO/PEDOT:PSS/MAPbI3\\u2212xClx/PCBM/LiF/Al. ITO slides (10 \\u03a9 per sq., CSG Holding Co., Ltd.) were sonicated sequentially in detergent, Milli-Q water, acetone, ethanol and isopropanol for 10 min each. After being dried, the slides were treated with UV-ozone for 20 min. On the freshly cleaned ITO substrates, PEDOT:PSS (Clevios P VP Al 4083, filtrated with a 0.45 \\u03bcm nylon filter) was spin-coated and annealed at 150 \\u00b0C for 15 minutes. The perovskite precursor was deposited on top of PEDOT:PSS by spin-coating at 3000 rpm for 50 s. Then the perovskite layer was treated by rtMSVA or TA methods. (1) rtMSVA treatment. The sample plates of the spin-coated pero-TFs were put in Petri dishes (with a cover but not sealed) with vapors of mixed solvents of DMF and chlorobenzene (CB) with defined volume ratios. The treatment was performed at room temperature without touching the mix-solvent. The color of the pero-TFs turned from yellow to dark brown in a few minutes. The optimized duration was approximately 6 minutes. To obtain high-performance pero-SCs, the rest of the layers of the devices were not immediately covered atop of the pero-TF after the rtMSVA, but we waited for a period of approximately 12 h to allow any remaining trace amount of the solvent to dry off. (2) TA treatment. As a control, the TA process was conducted by putting the specimens on a hot plate maintained at 95 \\u00b0C for 70\\u221280 minutes. After the rtMSVA or TA treatments, PCBM (15 mg mL\\u22121 in chloroform) was spin-coated at 1200 rpm for 60 s on the pero-TF layers. Then, LiF (\\u223c1 nm) and aluminum (\\u223c100 nm) were sequentially capped on the PCBM layer by vacuum deposition, with a shadow mask clung to the substrates to define the active areas.\\nLAA flexible pero-SCs (with an active area of 1.21 cm2) on a flexible PET/Ag-grid/PH1000 electrode were also fabricated by a similar method as that on an ITO substrate. The device configuration was PET/Ag-grid/PH1000/PEDOT:PSS/MAPbI3\\u2212xClx/PCBM/LiF/Al. Note that herein the PET/Ag-grid (supplied by Prof. Zheng Cui) together with a layer of conducting polymer PH1000 was used as the flexible electrode. PET was employed as the flexible support, and the Ag nanoparticles were embedded in the groove-grid carved on the surface of PET. The nominal sheet resistance of the PET/Ag-grid was 2.1 \\u03a9 per sq. PH1000 (Clevios) with 5 wt% DMSO was spin coated on the PET/Ag-grid at 600 rpm for 60 s, followed by annealing at 120 \\u00b0C for 20 min. The remaining operations in the preparation of the flexible pero-SCs are the same as that of the pero-SCs on the ITO substrate.\\n\\nThe time-dependent absorption spectra of pero-TFs during rtMSVA treatment were measured on a Cary 5000 (Agilent) instrument. In order to make a parallel comparison and avoid the influence of ITO, the pero-TFs were deposited on glass/PEDOT:PSS substrates. XRD patterns were collected using an X'Pert-Pro MRD diffractometer (Panalytical). A field emission scanning electron microscope (FE-SEM, S-4700, Hitachi, Japan) was used for morphology observations. The J\\u2013V curves of the pero-SCs were measured in a glovebox on a Keithley 2400 source meter unit under standard air-mass 1.5 global (AM 1.5G, 100 mW cm\\u22122) illumination calibrated by a standard Si-SC. EQE of the devices were measured using a QE-R3011 (Enli Technology Co., Ltd.), where the light intensity was calibrated by a standard Si-SC.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 95,\\n Perovskite_deposition_thermal_annealing_time: 75,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine doped tin oxide coated (FTO) glasses (SnO2/F, \\u223c8 \\u03a9 sq\\u22121, Aldrich) were used as the transparent electrode and substrate of the devices, which were etched using zinc powder (Zn, Sigma-Aldrich, 98%) and hydrochloric acid (HCl, Alfa-Aesar) solution to form the desired pattern. The patterned FTO substrates were subsequently cleaned in ultrasonic baths (Branson 1500) containing mucasol (Sigma-Aldrich), de-ionized water, methanol (Alfa-Aesar), acetone (Alfa-Aesar) and 2-propanol (J.T.Baker), respectively (each for 10 minutes). Afterwards, the substrates were dried with nitrogen, followed by heat treatment at 120 \\u00b0C for 20 mins to remove the last traces of any solvent. A hole transporting layer was deposited on the cleaned FTO substrate at 3000 rpm for 1 min using a PEDOT:PSS (AI 4083, HERAEUS) solution in 2-propanol (J.T.Baker) (1:3 ratio), which was annealed at 150 \\u00b0C for 20 min. To form the active layer of perovskite, a precursor solution of MAPbI3\\u2212xClx was prepared by dissolving equimolar ratios of lead iodide (PbI2, Sigma-Aldrich, 99%) and methylamine hydrochloride (MACl, Sigma-Aldrich) in N,N-dimethylformamide (DMF, Sigma-Aldrich, anhydrous, 99.8%) in a concentration of 11 wt%. The perovskite films were fabricated using a hot-casting technique in which the substrates were kept at 180 \\u00b0C and the precursor solution at 70 \\u00b0C. The solution was then immediately spin-coated on top of the hot PEDOT:PSS layer so that the substrate temperature was retained. Then, the devices were transferred to a nitrogen-filled glove box. PCBM, used as an ETL, was spun on top of the perovskite layer at 1250 rpm for 60 s using a solution of 2 wt% PCBM (Nano-C, 99.5%) in 1,2-dichlorobenzene (Alfa-Aesar, 99%). C60 or carbon was deposited on top of the PCBM layer at a base pressure of <1 \\u00d7 10\\u22127 Torr. Particularly, C60 (Alfa Aesar, 99%) or graphite (Aldrich, 99.99%) was placed in a graphite crucible and irradiated by e-beam. The resultant thickness and morphologies were measured by SEM. Finally, 170 nm thick silver (Alfa-Aesar, 99.9%) as a cathode electrode was deposited at 4 angstroms per second under a pressure of 1 \\u00d7 10\\u22127 Torr using an electron beam (E-beam) evaporator. In this study, the reference perovskite solar cell was FTO/PEDOT:PSS/MAPbI3\\u2212xClx/PCBM/Ag. To study the effectiveness of the PCBM/carbon and PCBM/C60 layers for photovoltaic performance, two different perovskite solar cells of FTO/PEDOT:PSS/MAPbI3\\u2212xClx/PCBM/C60 (\\u223c10 nm)/Ag and FTO/PEDOT:PSS/MAPbI3\\u2212xClx/PCBM/carbon (\\u223c10 nm)/Ag were fabricated, as shown in Fig. 1(a). All of the three devices have an active area of 10 mm2.\\n\\nPerovskite samples were prepared on glass substrates to attain optical characterization of steady-state and time-resolved PL. The cleaning steps of the glass substrates and the deposition procedure of the perovskite layer were the same as mentioned for the perovskite solar cells. To prevent degradation by air exposure, the samples were coated by a polymer, polymethyl-methacrylate (PMMA, Sigma-Aldrich, Mw \\u223c 120000) in chlorobenzene (Sigma-Aldrich, 99.5%) (10 mg ml\\u22121), at 2000 rpm for 30 s. The steady-state and time-resolved PL spectra were recorded using a spectrophotometer (Flurolog, Horiba Jobon Yvon) and a time-correlated single photon counting (TCSPC) system connected with a solid-state laser. For the PL measurement, an excitation wavelength of 450 nm was used and the emission spectra were measured from 600 nm to 850 nm. For the time-resolved PL (TRPL), a high-speed photomultiplier tube detector (FL-1073, Horriba scientific Inc.) was employed for photon counting with a repetition rate of 4 MHz and 450 nm excitation.\\n\\nSurface and cross-sectional scanning electron microscope (SEM) images of the perovskite film were collected by a Hitachi S-4700 field emission SEM (FESEM). Images were taken at different magnifications and accelerating voltages. A thin conductive layer of gold (Au) was coated on the film using a Hummer V Sputter Coater before scanning the surface and cross-section of the film. The sheet resistance of the perovskite film was measured using a Jandel RM3 four-point probe. In addition, an Ecopia HMS-5300 Hall effect measurement system was used to determine electrical properties such as sheet resistance, mobility, resistivity, Hall coefficient, and so on.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | C60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.001,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All solvents and reagents, if not specified, were purchased from commercial chemical suppliers and used without further purification.\\nCH3NH3PbI3\\u2212xClx perovskite precursor solution was prepared as reported in literature procedures. CH3NH3I (lumtech) 381.5 mg and PbCl2 (99% Aldrich) 222.5 mg were mixed in a molar ratio of 3:1 in 1 mL of DMF (99% Aldrich) at 70 \\u00b0C and stirred overnight. Poly-(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) Al-P 4083 was purchased from Heraeus. PC61BM was from Merck Chemicals. ZnO nanoparticles were synthesized as reported.\\n\\nThe ITO-coated glass substrates (sheet resistance 10 \\u03a9 \\u25a1\\u22121, Pilkington) were cleaned in an ultrasonic bath of detergent, acetone, isopropanol and ethanol for 15 min each. The ITO-patterned PET substrates (from CP-films) were washed with isopropanol with a sprayer. After being dried by a nitrogen flow, they were treated with UV-ozone for 15 min to remove the traces of organic residues.\\n\\nThe cleaned ITO glass substrates were spin-coated with PEDOT:PSS AL-P 4083 at 3000 rpm for 40 s, followed by heating at 140 \\u00b0C in air for 15 min. The PEDOT:PSS coated substrates were then transferred into a N2 glovebox for further processing. The perovskite precursor was spin-coated on the PEDOT:PSS layer at 2500 rpm for 40 s. After spin-coating, the films were annealed on a hotplate in the dark at 100 \\u00b0C for 120 min. 40 mg mL\\u22121 PC61BM in chlorobenzene and the ZnO nanoparticle solution was then deposited on the CH3NH3PbI3\\u2212xClx film by spin-coating at 1000 rpm for 60 s and 2000 rpm for 40 s respectively. Finally, a 150 nm-thick Ag electrode was deposited by vacuum evaporation through a shadow mask to define an active device area of 0.055 cm2. All device measurements were conducted in air with a humidity of 25%.\\nThe SEM images were obtained from an S-4800 (Hitachi) field-emission scanning electron microscope (FESEM). The samples were fractured in liquid nitrogen before measurement. The X-ray diffraction (XRD) measurement was conducted by a Rigaku D/max 2550/PC X-ray diffractometer using graphite monochromatic CuK\\u03b1 radiation. UV-vis absorption spectra were recorded by using a UV-2450 UV-vis Shimadzu spectrophotometer. Photocurrent\\u2013voltage (I\\u2013V) curves of the unsealed samples were measured in air on a Keithley 2400 unit, under AM 1.5 G circumstance provided by using an ABET SUN2000 simulator at 100 mW cm\\u22122, calibrated with a standard Si reference cell (Radboud University Nijmegen). To minimize the influence of device degradation caused by moisture corrosion, the I\\u2013V characterization was carried out immediately after the device fabrication. The incident photon conversion efficiency (EQE) spectra were recorded by using a 71SW303 data collector.\\n\\nThe devices were fabricated on a roll of flexible polymer substrates with patterned ITO. During the roll-coating, the flexible substrates were kept at 40 \\u00b0C, and the whole procedure was performed in air. Solutions for roll-coating were transferred to a slot-die head via a syringe pump. First the PEDOT:PSS AL-P 4083 was employed at a flow rate of 0.08 mL min\\u22121 and a web speed of 0.5 m min\\u22121 followed by 10 min 110 \\u00b0C annealing to form a 30 nm-thick hole transport layer. In order to obtain uniform films, the PEDOT:PSS was diluted with isopropanol in the ratio of 3:1 (v/v) to improve the wetting effect. The perovskite precursor was then coated on the PEDOT:PSS layer at a flow rate of 0.017 mL min\\u22121 and a web speed of 0.5 m min\\u22121. After the perovskite films dried, the foil was annealed in an oven at 110 \\u00b0C for 30 min. Two methods were employed to deposit the electron transport layer. 40 mg mL\\u22121 PC61BM CB solution and ZnO nanoparticle isopropanol solution were either roll-coated at flow rates of 0.03 m min\\u22121 and 0.02 m min\\u22121, respectively, on the annealed perovskite films, or spin-coated at 1000 rpm and 2000 rpm, respectively, on 1.5 cm \\u00d7 3 cm pieces of substrates that were cut off from the annealed perovskite foil. Finally, a 150 nm-thick Ag electrode was deposited by vacuum evaporation through a shadow mask to define an active device area of 0.5 cm2. The devices were sealed with 3M foil before testing.\\nThe atomic force microscopy (AFM) images were taken on a Veeco Multimode atomic force microscope in the tapping mode. Photocurrent\\u2013voltage (I\\u2013V) curves of the sealed samples were measured in air (humidity \\u223c 20%) on a Keithley 2400 unit, under AM 1.5 G circumstance provided by using a KHS 575 solar simulator at 100 mW cm\\u22122, calibrated with a standard Si reference cell. The forward bias to short-circuit voltage sweep was conducted from \\u22120.1 to 1.0 V with voltage steps of 5 mV. The external quantum efficiency (EQE) spectra were measured using a Solar Cell Spectral Response Measurement System QEX10.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 120,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.055,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the chemicals were used as received, including PbI2 (99.9985%, Alfa Aesar), MAI, FAI (Xi'an Polymer Light Technology Corp.), cesium acetate (99.99%, Alfa Aesar), anhydrous cesium iodide (99.999%, Alfa Aesar), SnCl2\\u00b72H2O (98\\u2013103%, Alfa Aesar), and spiro-OMeTAD (99.7%, Lumtec Co., Taiwan). 4-tert-Butylpyridine (TBP, 96%), bis(trifluoromethane)sulfonimide lithium salt (99.95%), and solvents of acetonitrile (99.9%), ethanol (99.8%), dimethylformamide (DMF, 99.8%), dimethylsulfoxide (DMSO, 99.9%), and chlorobenzene (99.8%) were all purchased from Sigma Aldrich. FTO glasses (FTO, 7 \\u03a9 sq\\u22121) were purchased from Yingkou OPVtech New Energy Co. Ltd.\\n\\nThe synthesis of SnO2 gel has been conducted by our group, which is summarized as follows: SnCl2\\u00b72H2O solution (0.1 M) was prepared by dissolving SnCl2\\u00b72H2O in anhydrous alcohol in a flask. Then the solution was stirred at 80 \\u00b0C with the neck of the flask sealed to prevent entry of O2 and H2O into the solution for 3 h. To obtain SnO2 organic sol, the just dissolved SnCl2\\u00b72H2O solution was transferred to an open reflux apparatus, with refluxing for another 6 h at 40 \\u00b0C. When the reaction was over, the product was aged for over 24 h at room temperature. To prepare SnO2 ETLs, SnO2 sol was spin-coated on FTO at 2000 rpm for 30 s, and then heated at different temperatures for 1.5 h to remove solvent. Then, the as-deposited ETLs were treated with UV-ozone for 30 min. Both pristine and Cs4SnO4-modified devices were made by using blank SnO2 film, while Cs4SnO4-modified SnO2 film was made using 4 mM aqueous cesium acetate (CsAc). First, a sol-SnO2 layer on FTO was heated at 100 \\u00b0C for 1 hour. After cooling down to the room temperature, this layer was subsequently covered with an aqueous CsAc film by spin-coating and then annealed at 100 \\u00b0C for another 0.5 hour in air. Last, the as-deposited Cs4SnO4-modified ETLs were treated with UV-ozone for 30 min.\\n\\n(FAPbI3)0.85(MAPbBr3)0.15 precursor was synthesized as described by the Hagfeldt group. First, an anhydrous mixture of DMF and DMSO (volume ratio is 4:1) containing FAI (1 M), PbI2 (1.1 M), MABr (0.2 M) and PbBr2 (0.2 M) was prepared firstly by stirring at 70 \\u00b0C for 2 h. Then, 80 \\u03bcL solution was spread on the FTO/ETL substrate followed by a two-stage spin-coating process (1000 rpm for 10 s and 6000 rpm for 50 s). During the second spin-coating stage, 100 \\u03bcL of chlorobenzene was poured on the spinning substrate 15 s prior the end of the program. Finally, the perovskite films were annealed at 100 \\u00b0C for 40 min, then both pristine and Cs4SnO4-modified film types were obtained. Cs0.06FA0.8MA0.14Pb(I0.85Br0.15)3 precursor was synthesized with 1.5 M CsI DMSO solution and (FAPbI3)0.85(MAPbBr3)0.15 precursor (volume ratio = 5:95). Cs0.06FA0.8MA0.14Pb(I0.85Br0.15)3 is denoted as bulk CsFAMA. (FAPbI3)0.85(MAPbBr3)0.15 film fabricated with bare SnO2 and Cs4SnO4-modified SnO2 is denoted as pristine FAMA and Cs-modified FAMA, respectively.\\n75 mg mL\\u22121 spiro-OMeTAD (Borun New Material Technology Co. Ltd.), the HTM, was dissolved in chlorobenzene. 28.8 \\u03bcL of TBP and 17.5 \\u03bcL of a 520 mg mL\\u22121 LiTFSI solution were added to the OMeTAD solution as additives. The HTM layer was applied onto the perovskite by a 4000 rpm 25 s spin-coating process. The Au (50 nm) electrode was deposited through a shadow mask (3 \\u00d7 4 mm2) by thermal evaporation.\\n\\nThe TRPL spectra were measured using an Edinburgh Instruments FLS920 spectrometer by the time correlated single photon counting technique. An EPL 460 nm pulsed diode laser was used for excitation with repetition rates at 10 MHz. The maximum average power was 5 mW and all samples were measured at the same intensity. The emission wavelength was set at 765 nm. The photocurrent\\u2013voltage (J\\u2013V) characteristics of the devices were measured with a Keithley 2400 digital source meter at a scan speed of 100 mV s\\u22121. The simulated AM 1.5G sunlight with an irradiance equivalent to 100 mW cm\\u22122 was generated by a Oriel Solar 3A solar simulator and the intensity was calibrated with a VLSI standards-incorporated PN 91150V Si reference cell. The cells were masked using a black metal mask with a hole area of 0.096 cm2. Steady-state output of photocurrent and PCE were measured with a Keithley 2400 digital source meter under a certain bias. The IPCE spectra were recorded by a setup consisting of a xenon light source, a monochromator, and a potentiostat. The crystal structures of ETLs were characterized using a Bruker D8 ADVANCE X-ray diffractometer. TEM and HRTEM analysis was carried out with a JEOL JEM-2100F microscope. Samples for analysis were obtained by sonicating the peeled-off SnO2 into ethanol, and then drop-casting the solution onto carbon-coated copper TEM grids at room temperature. SEM images were acquired with a field-emission scanning electron microscope (FE-SEM, JEOL JSM-7401F). UV-visible absorption spectra were recorded via an HPX-2000 (Ocean Optics). XPS measurements were performed with equipment made in the UK (ESCALAB 250Xi). The ToF-SIMS measurements (model TOF-SIMS 5-100, ION-TOF GmbH) were performed with pulsed primary ions from a O2+ (1 keV) ion gun for the sputtering and a Bi+ pulsed primary ion beam for the analysis (30 keV). UPS characterizations were performed with monochromatized HeI radiation at 21.22 eV. The space-charge-limited current as a function of the applied voltage was measured using a Keithley 2400 digital source meter, using an ETL/perovskite/Au structure. The samples (blank FAMA, Cs4SnO4-modified FAMA or bulk CsFAMA) were measured in a dark environment at 300 K.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.096,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials and methods. All chemicals were purchased from Aldrich and used as received, unless otherwise specified. UV-vis absorption spectra were recorded using a Hitachi U-3300 spectrophotometer. MAI was synthesized according to a previously reported procedure.\\nDevice fabrication and characterization. Perovskite-based PV cells were prepared using the following device fabrication procedure. Glass/ITO substrates [Sanyo, Japan (8 \\u03a9 \\u25a1\\u22121)] were sequentially patterned lithographically, cleaned with a detergent, ultrasonicated in acetone and isopropyl alcohol, dried on a hot plate at 140 \\u00b0C for 10 min, and treated with oxygen plasma for 5 min. PEDOT:PSS (Baytron P-VP AI4083) was passed through a 0.45 \\u03bcm filter and deposited onto ITO (thickness: ca. 40 nm) through spin-coating at 3000 rpm in air; the sample was then dried at 140 \\u00b0C for 20 min inside a glove box. The perovskite precursor solution was prepared by dissolving MAI and lead(II) chloride at ratio of 3:1 (molar ratio) at different concentrations in DMF and continuously stirring at 60 \\u00b0C in the dark overnight. Perovskite devices, having the layered configuration glass/ITO/PEDOT:PSS/CH3NH3PbI3\\u2212xClx/PC61BM/Al, were fabricated using methods similar to those reported previously. Prior to deposition of the perovskite layer, the PEDOT:PSS film was preheated at 60 \\u00b0C for 5 min. The precursor solution was also preheated at 60 \\u00b0C for 5 min and then deposited on top of the PEDOT:PSS. PCBM was spin-coated (2000 rpm) from a chlorobenzene solution (10 mg mL\\u22121). The layers of Al (100 nm) were deposited thermally under vacuum. The active area of the device was 10 mm2. The cell performance was measured inside a glove box. The current\\u2013voltage (I\\u2013V) properties of the devices were measured using a computer-controlled Keithley 2400 source measurement unit (SMU) and a Newport solar simulator (Oriel\\u00ae Sol2A Class ABA Solar Simulators) under AM 1.5 illumination (100 mW cm\\u22122). The illumination intensity was calibrated using a standard Si reference cell and a KG-5 filter. EQEs were measured using an Enlitech QE-R spectral response measurement system to calibrate the current densities of the devices. Morphologies of the polymer films were analyzed by AFM using a VEECO DICP-II instrument operated in tapping mode at ambient temperature; the etched Si probe exhibited a resonant frequency of 131 kHz and a spring constant of 11 N m\\u22121. GIWAXS patterns were collected on Philips Panalytical-X'PertPROMRD, the incident beam angle was above the critical angle (\\u223c0.5\\u00b0).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (CH3NH3I, MAI) was purchased from Dyesol Ltd (Australia). 2,2\\u2032,7,7\\u2032-Tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifluorene (Spiro-OMeTAD) was purchased from Borun Chemicals Co., Ltd. (Ningbo, China). [6,6]-Phenyl-C61-butyric acid methyl ester (PCBM) was purchased from Luminescence Technology Co. All the other materials, unless specified, were purchased from either Alfa Aesar or Sigma-Aldrich, and used as received without further purification.\\n\\nFluorine-doped tin oxide (FTO, sheet resistance \\u223c10 \\u03a9 \\u25a1\\u22121) substrates were ultrasonically cleaned with deionized water, acetone, and isopropyl alcohol for 15 min each sequentially. Then, they were further cleaned with ultraviolet ozone treatment (UV-O3) for 15 min before device fabrication.\\nFor PSCs with the n\\u2013i\\u2013p configuration: the compact TiOx and FeOx electron extraction layer (EEL) was fabricated by spin-coating an acidic ethanol solution (0.12 M) of titanium isopropoxide and iron(III) nitrate nonahydrate (Fe(NO3)3\\u00b79H2O), respectively, at 4000 rpm for 40 seconds. The substrates were subsequently heated at 100 \\u00b0C for 30 min and further annealed at 500 \\u00b0C for 1 hour. We then spin-coated an 8 mg mL\\u22121 solution of PCBM in chlorobenzene at 4000 rpm for 30 s for passivating the TiOx surface. This modified TiO2 is denoted as TiOx(m). A perovskite layer with a composition of CH3NH3PbI3 was deposited by spin-coating the precursor solution composed of CH3NH3I and lead iodide (PbI2) (molar ratio of 1:1; 1.35 M) in a mixed solvent of N,N-dimethylformamide (DMF) and dimethyl sulphoxide (DMSO) (with a volume ratio of 7:3) onto the EEL at 5000 rpm for 60 s. Meanwhile, chlorobenzene was quickly dropped onto the center of the substrate for 10 s after the spin-coating commences. The as-deposited film was then heated at 100 \\u00b0C for crystallization for 15 min. Spiro-OMeTAD solution, consisting of 72.3 mg of Spiro-OMeTAD, 17.5 \\u03bcL of bis(trifluoromethane)sulfonimide lithium salt (LiTFSI) in acetonitrile (520 mg mL\\u22121), and 28.8 \\u03bcL of 4-tert-butylpyridine (TBP) in 1 mL of anhydrous chlorobenzene, was spin-coated onto the CH3NH3PbI3 layer at 4000 rpm for 40 s to form the HEL. Finally, a Au electrode with a thickness of around 90 nm was deposited on top of the HEL by thermal evaporation for the n\\u2013i\\u2013p structured PSCs.\\nFor PSCs with the p\\u2013i\\u2013n configuration: A NiOx compact hole extraction layer (HEL) was fabricated by spin-coating a solution of nickel(II) nitrate hexahydrate (Ni(NO3)2\\u00b76H2O) in anhydrous ethanol (0.1 M) at 4000 rpm for 30 s twice. Before the second spin-coating, the film was dried at 80 \\u00b0C for 15 min. Afterwards, the film was sintered at 350 \\u00b0C for 30 min. The preparation method of the perovskite layer is the same as that mentioned for the n\\u2013i\\u2013p structured PSC fabrication. Then, PCBM in anhydrous chlorobenzene (20 mg mL\\u22121) was spin-coated onto the CH3NH3PbI3 layer at 2000 rpm for 40 s to prepare the EEL for the p\\u2013i\\u2013n structured PSCs. As the final step, silver with a thickness of about 120 nm was thermally evaporated onto the EELs to fabricate a top electrode for the p\\u2013i\\u2013n PSCs.\\n\\nThe film morphology and thickness information were obtained using a field emission scanning electron microscope (FESEM, EHT = 5.0 kV, WD = 6.5 mm, Zeiss LEO1530, Germany). Ultraviolet-visible absorption and transmission spectra were recorded using a Lambda 950 spectrophotometer at room temperature with an integrating sphere detector (250\\u2013800 nm, PerkinElmer, USA). Steady-state and transient PL decay spectra were obtained using an FLS920 transient optical spectrometer. Steady-state PL measurements were measured by exciting the sample using a monochromatic xenon lamp source with a central wavelength of 460 nm. Time-resolved PL measurements were performed using a time-correlated single-photon counting (TCSPC) system. Samples were photoexcited using a 405 nm laser beam (EPL405), pulsed at frequencies between 10 and 20 MHz, with a pulse duration of <100 ps and the maximum fluorescence intensity. The J\\u2013V characteristics of the linear voltage scan and stepwise voltage scan were measured using a digital source meter (2400, Keithley Instruments, USA) under AM 1.5G illumination, with the device illuminated by a solar simulator (91192, Oriel, USA). The light intensity was calibrated with a standard crystalline silicon solar cell (PT-SI-RSC, Pharos Technology). The active area (0.06 cm2) of the devices for photovoltaic J\\u2013V measurement was determined by a metal aperture.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The material CH3NH3I (MAI) was synthesized based on the literature. In short, to prepare MAI, hydroiodic acid (10 mL, 57 wt% in water, Sigma-Aldrich) and methylamine (10 mL, 33 wt% in absolute ethanol, Sigma-Aldrich) were reacted in a round bottomed flask in ice-cold water with stirring for 60 min. Raw CH3NH3I was obtained by removing the solvent at 50 \\u00b0C on a rotary evaporator. The material was then washed in diethyl ether and filtered several times. The precipitate was then dried in a vacuum oven overnight at 50 \\u00b0C and then stored in nitrogen-filled glovebox.\\n\\nThe evaporation was carried out in Angstrom Engineering EvoVac deposition system with integrated Innovative Technology glovebox. The PbCl2 and MAI materials were both evaporated from ceramic crucibles. The evaporation rate was monitored by the quartz crystals. The quartz crystals could be reused after dipping in DMF solution and then washing in ethanol. New quartz crystal was used for each evaporation. The undulating evaporated CH3NH3I film makes it difficult to measure the accurate thickness. To avoid the tedious calibration process for the evaporation (or deposition) rate of each material, we set the tooling factor (which is a ratio of the film deposition rate monitored by sensor to that on the substrate) to be 100% during all the co-evaporation process. Initially, the evaporator sources were heated slowly to an level that the evaporation rate was just around the desired range, the process were then carried out in auto mode. A desired evaporation rate can be obtained via heating control system from the feedback of their sensors. After the evaporation rate were stabilized for a prolonged time, the PbCl2 film and MAI film were then co-evaporated onto the substrates with substrate baffle open. Various MAI evaporation rate (0\\u20138 \\u00c5 s\\u22121) were employed. The evaporation rate of PbCl2 material was maintained at constant monitored rate of 2 \\u00c5 s\\u22121.\\n\\nSolar cells with FTO/PEDOT:PSS/Perovskite/PCBM/Ag planar device structure were prepared. Before deposition of other films, the FTO-coated glass substrates were ultrasonically cleaned with detergent, deionized water, acetone and ethanol sequentially, and were then blow-dried in nitrogen. After that, PEDOT:PSS solution (Clevious Al 4083) was spin-coated on FTO-coated substrates at 2000 rpm for 45 s, and subsequently the PEDOT:PSS films were annealed at 150 \\u00b0C for 20 min. After cooling down, perovskite absorbers were evaporated on PEDOT:PSS films. The evaporated perovskite films were then annealed at 100 \\u00b0C for 45 min on a hot plate. 30 mg ml\\u22121 PCBM (FEM. Inc.) solution in chlorobenzene (Sigma-Aldrich) was then spin-coated at 1000 rpm for 45 s. Finally, Ag top contact was deposited by evaporation through an aperture mask under a base pressure of 7 \\u00d7 10\\u22126 Torr. The active device area is 0.12 cm2.\\n\\nX-ray diffraction (XRD) analysis was performed on a D/max-RB diffractometer (Rigaku) using Cu K\\u03b1 radiation at a scan rate of 6\\u00b0 min\\u22121. The energy-dispersive X-ray (EDX) compositions and spectra were performed using energy-dispersive spectroscopy (EDS) combined with a field-emission scanning electron microscope (SEM, Hitachi S4500). SEM images were obtained using Hitachi S4500 and Hitachi S5200. Film absorbance spectra were measured by Shanghai UV-vis SP-752 spectrometer. Current\\u2013voltage measurements and power conversion efficiencies were obtained using Keithley 2400 at room temperature under AM 1.5G illuminations (1000 W m\\u22122) from a solar simulator which was calibrated using a standard silicon solar cell device.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: none,\\n Perovskite_deposition_procedure: Co-evaporation,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"1H and 13C NMR spectra were recorded on a Brucker Advance 500 spectrometer (500 MHz). The deuterated solvents are indicated in the synthesis description. Chemical shifts, \\u03b4, are given in ppm, using the solvent residual as an internal standard. MS were recorded on Micro-Tof using electrospray ionisation (ESI) technique. Elemental analyses were carried out by Stephen Boyer at London Metropolitan University.\\n\\nSolution UV-visible absorption spectra were recorded using a Jasco V-670 UV/Vis/NIR spectrometer controlled with SpectraManager software. Photoluminescence (PL) spectra were recorded with a Fluoromax-3 fluorimeter controlled by ISAMain software. All samples were measured in a 1 cm cell at room temperature in dichloromethane as solvent. Concentrations of 2.5 \\u00d7 10\\u22125 M and 1 \\u00d7 10\\u22126 M were used for UV/Vis and PL respectively.\\nCrystallographic details. Powder diffraction was performed on a Bruker Discover D8 with CuKa1/2 source and a scintillation detectior 4860.\\nSingle yellow block-shaped crystals of EtO-DATPA were recrystallised from benzene by slow evaporation. Single orange block-shaped crystals of iPrO-DATPA were recrystallised from benzene by slow evaporation. Single yellow plate-shaped crystals of nPrO-DATPA were recrystallised from a mixture of DCM and hexane by slow evaporation. Single orange block-shaped crystals of BuO-DATPA were recrystallized from benzene by slow evaporation. A suitable crystal of EtO-DATPA (0.24 \\u00d7 0.16 \\u00d7 0.14), iPrO-DATPA (0.51 \\u00d7 0.23 \\u00d7 0.10), nPrO-DATPA (0.55 \\u00d7 0.29 \\u00d7 0.09) and BuO-DATPA (0.25 \\u00d7 0.24 \\u00d7 0.14) were selected and mounted on a MITIGEN holder in Paratone oil on a Rigaku Oxford Diffraction SuperNova diffractometer. The crystal was kept at T = 120.0 K during data collection. Using Olex2 (Dolomanov et al., 2009), the structure was solved with the ShelXS (Sheldrick, 2008) structure solution program, using the Direct Methods solution method. The model was refined with version of ShelXL (Sheldrick, 2008) using Least Squares minimisation. A summary of the data collection and structure refinement is reported in Table S4 (ESI\\u2020).\\n\\nDifferential scanning calorimetry (DSC) was performed on NETZSCH STA 449F1 at a scan rate of 5 K min\\u22121 under a nitrogen atmosphere in DSC/TG aluminium pan. The measurement range was 25 \\u00b0C to 250 \\u00b0C.\\n\\nAll cyclic voltammetry measurements were carried out in freshly distilled CH2Cl2 using 0.3 M [TBA][BF4] electrolyte in a three-electrode system with each solution being purged with N2 prior to measurement. The working electrode was a Pt disk, the reference electrode was Ag/AgCl, and the counter electrode was a Pt rod. All measurements were made at room temperature using a \\u03bcUTOLAB Type III potentiostat, driven by the electrochemical software GPES. Cyclic voltammetry (CV) measurements used scan rates of 100 mV s\\u22121: square wave voltammetry (SWV) was carried out at a step potential of 4 mV, square wave amplitude of 25 mV, and a square wave frequency of 10 Hz, giving a scan rate of 40 mV s\\u22121. Ferrocene was used as the internal standard in each measurement.\\n\\nAll calculations were carried out using the Gaussian 09 program with Lee\\u2013Yang\\u2013Parr correlation functional (B3LYP) level of theory. All atoms were described by the 6-31G(d) basis set. All structures were input and processed through the Avogadro software package.\\n\\nThe Ossila low-density pre-fabricated substrates (channel length 0.1 mm width 0.03 mm) with a bottom gate/bottom contact were used to fabricate OFET devices. The substrates were treated with HMDS (hexamethyldisilazane) to optimise the silicon surface property. A solution of the HTM (5 mg ml\\u22121) in dichlorobenzene was stirred at room temperature. The Ossila substrate was covered with the solution by drop-casting. The electric characteristics of the fabricated OFETs were measured using a Keithley 2612A System SourceMeter. Mobilities were calculated using the following equation\\nwhere Z is the channel width, L the channel length, Ci the capacitance, VG the gate voltage and IDS is the drain current and , the slope of the transfer characteristic curves in the saturation regime.\\n\\nSample preparation. A solution of mesoporous TiO2 in terpineol (Dyesol 30 nm TiO2, weight ratio 1:2) was spin coated on a 10 mm by 10 mm glass square, with an acceleration of 12000 rpm for 30 s. The pieces of glass were cleaned with isopropanol (IPA) in a sonicator for 5 minutes before spin coating. After spin coating, the substrates were placed into a 450 \\u00b0C oven for 1 hour and cooled down to room temperature before deposition of the perovskite layer. For the deposition of the perovskite layer 1 M solution of PbI2 and MeNH3I in DMSO was prepared. This solution was spin-coated onto the glass slides covered with the mesoporous oxide via a 3-step spin coating process: (i) 1000 rpm, 10 s, 2000 acc; (ii) 5000 rpm, 20 s, 2000 acc; (iii) 6000 rpm, 20 s, 2000 acc. Toluene (300 \\u03bcL) was dropped on the substrates by the end of the second step. The films were then annealed at 50 \\u00b0C for 20 min and at 100 \\u00b0C for 25\\u201330 min and cooled down to room temperature. A 20 mg ml\\u22121 solution in chlorobenzene of the corresponding HTM was spin-coated onto the perovskite layer at 200 rpm for 30 s, with an acceleration of 2000.\\nMeasurements. UV-Vis was performed on a PerkinElmer UV/VIS Spectrometer Lambda 25. Photoluminescence spectra were recorded on a Horiba Yobin-Ybon Fluorolog-3 spectrofluorometer, using an excitation wavelength of 450 nm and slit widths of 10 nm. For pump\\u2013probe micro to millisecond transient absorption spectroscopy, films were excited by a dye laser (Photon Technology International GL-301, sub-nanosecond pulse width) pumped by a pulsed nitrogen laser (Photon Technology International GL-3300). A quartz halogen lamp (Bentham IL1) was passed through a monochromator and used to probe changes in the absorption characteristics of the film as a function of time after the laser excitation. The probe light was detected using home-built silicon (\\u22641000 nm) or InxGa1\\u2212xAs (>1000 nm) photodiodes and an oscilloscope. Unless otherwise stated, films were kept under flowing N2 during the measurements. All micro to millisecond transient absorption spectroscopy measurements were conducted employing 450 nm laser pulses (25 \\u03bcJ cm\\u22122).\\n\\nEtched FTO glass substrates (NSG Pilkington, TEC7) were cleaned sequentially in detergent, deionised water, acetone and ethanol before undergoing 10 minutes of O2 plasma treatment. A compact TiO2 layer was deposited on the glass substrates through spray pyrolysis of a 0.2 M solution of titanium diisopropoxide bis(acetylacetonate) in isopropanol at 450 \\u00b0C. Upon cooling, a mesoporous layer of TiO2 nanoparticles was spin-coated from a 2:7 wt suspension of Dyesol 30NR-D paste in ethanol (4500 rpm for 30 seconds), followed by sintering at 550 \\u00b0C for 30 minutes. A CH3NH3PbI3 perovskite precursor solution was prepared by dissolving 576 mg PbI2, and 199 mg CH3NH3I in a 4:1 vol solution of DMF:DMSO. 100 \\u03bcl of the perovskite precursor solution was deposited onto the TiO2 films and spin-coated at 4000 rpm for 30 seconds, with 200 \\u03bcl of ethyl acetate dripped onto the spinning substrate 10 seconds prior to the end of the spin-coating process. Perovskite films were annealed at 100 \\u00b0C for 10 minutes. In the case of the spiro-OMeTAD HTM, a 85 mg ml\\u22121 solution of spiro-OMeTAD in chlorobenzene was prepared with dopants including bis(trifluoromethylsulfonyl)imide lithium salt (Li-TFSI) (20 \\u03bcl ml\\u22121 of a 520 mg ml\\u22121 solution in acetonitrile), 4-tert-butylpyridine (tBP, 30 \\u03bcl ml\\u22121) and tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)-cobalt(III) tris(bis(trifluorome-thylsulfonyl)imide) (FK209, 10 \\u03bcl ml\\u22121 of a 300 mg ml\\u22121 solution in acetonitrile). For other HTMs, the same weight of material was dissolved in chlorobenzene with 2 times the volume of additives included. The higher dopant concentration used for the DATPA HTMs was found to be beneficial due to the deeper HOMO level of these compared with spiro-OMeTAD. The HTM solution was spin-coated onto perovskite films at 4000 rpm for 30 seconds before 80 nm thick Au contacts were thermally evaporated onto devices.\\nCurrent\\u2013voltage measurements were performed using a AAA-rated solar simulator (Oriel Sol3A) calibrated against a KG5-filtered reference diode (Oriel 91150-KG5). Solar cells were masked to 0.1 cm2 and scanned both from forward to reverse bias and vice versa at 100 mV s\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: EtO-DATPA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I, PbI2 and PbCl2 were purchased from the Materials Co. in Canada and Alfa Aesar Co. in China. PbI2, PbCl2 and CH3NH3I3 (2 M:1 M:1 M) were dissolved in N,N-dimethylformamide (DMF; Aldrich Co.) as the precursor solutions. All of the precursor solutions were stirred at 80 \\u00b0C for 12 h, which when the mass concentration was 30 wt% gave polymeric precursor solution. The hole transport layer used PEDOT:PSS (AI4083, Sigma-Aldrich), purchased from Bayer Co., Germany. The electron transport layer used phenyl-C60-butyric acid methyl ester (PC60BM) material, purchased from Banhe Technology Co. The PC60BM concentration was 20 mg mL\\u22121, dissolved in chlorobenzene (Aldrich Co.), and stirred at 80 \\u00b0C for 6 h. Electrodes for anode and cathode were ITO and aluminum (Al) electrodes, respectively. The whole device structure is ITO/PEDOT:PSS/perovskite/PCBM/Al.\\n\\nFirstly, laser-patterned, ITO-coated glass substrates were cleaned by ultrasonic oscillation in an alkaline, aqueous washing solution for 15 min. Afterwards, they were rinsed successively with deionized water, ethanol and acetone, then placed into an O3 condition using ultraviolet treatment for 30 min. PEDOT:PSS was deposited by spin-coating at 5000 rpm for 30 s to give a thickness of 40 nm. All thickness measurements of thin films used surface step profilers (Brooker Co., Germany). Afterwards, the prepared perovskite (MAPbI3\\u2212xClx) was spin-coated on the PEDOT:PSS thin film at 1000 rpm for 10 s, followed by 4000 rpm for 35 s. The thin film was immediately annealed at 70 \\u00b0C for 80 min. After cooling down, PC60BM (20 mg mL\\u22121 in chlorobenzene) was spin-coated on top of the perovskite film at 2000 rpm for 45 s, followed by spin-coating an interface-modifying layer of PEIE (0.1 wt%, in anhydrous 2-propanol) at 5000 rpm for 60 s. Finally, 80 nm thick Al layers were thermally deposited as the top electrodes under a vacuum of 4 \\u00d7 10\\u22124 Pa to fabricate perovskite solar cells with an area of 9 mm2. All devices were encapsulated by epoxy resin in a glove box for experimental measurements. The device structure is shown in Fig. 1. The DIO (Aldrich) concentrations were 0.2, 0.6, 1.0 and 1.5 wt%, added into the perovskite polymeric material as the precursor solution, and heated with stirring for 12 h at 80 \\u00b0C.\\n\\nPhotovoltaic measurements were conducted using an AM 1.5 solar simulator equipped with a 450 W xenon lamp (Newport). The power output was adjusted to match AM 1.5 global sunlight (100 mW cm\\u22122 by using a reference Si solar cell). Current density\\u2013voltage (J\\u2013V) curves were obtained by applying an external bias to the cell and measuring the generated photocurrent with a Keithley model 2400 digital source meter. The voltage step and delay time of photocurrent were 10 mV and 100 ms, respectively. A similar data acquisition system was used to determine the monochromatic incident photon to electric current conversion efficiency. Under full computer control, light from a 300 W xenon lamp was focused through a Gemini-180 double monochromator onto the photovoltaic cell to be tested. The monochromator was incremented through the visible spectrum to generate IPCE(\\u03bb), defined by IPCE(\\u03bb) = 12400 (Jsc/\\u03bb\\u03c6), where \\u03bb is the wavelength, Jsc is the short-circuit photocurrent density (mA cm\\u22122), and \\u03c6 is the incident radiative flux (mW cm\\u22122). Photovoltaic performance was measured by using a metal mask with an aperture area of 10 mm2. The measurements were performed under bias light. The cross section of the device was measured by using a Zeiss Jemini FEG-SEM instrument at 5 kV with magnification of 250k.\\nFig. 2 shows the XRD patterns for the different DIO doping concentrations of 0.2, 0.6, 1.0 and 1.5 wt%. From the XRD results, we found that the pure perovskite shows several main peaks, the corresponding diffraction angles being 14.1\\u00b0, 28.4\\u00b0, 31.9\\u00b0, respectively. It is evident that the materials fabricated from perovskite solutions crystallize in a tetragonal crystal structure. XRD reflections confirm the MAPbI3\\u2212xClx perovskite structure with lattice parameters a = b = 8.8724 \\u00c5 and c = 12.5475 \\u00c5 for the control sample and a = b = 8.8650 \\u00c5 and c = 12.5370 \\u00c5 for the sample with 1% DIO additive. In addition, in the XRD pattern there also appears a small peak at 12.6\\u00b0, attributed to PbI2. When we added the DIO to the perovskite, the DIO additive has no effect on the perovskite phase structure, and no new peak appears. The DIO addition, on the one hand, makes the grain size of perovskite become larger; on the other hand, it increases the PbI2 grain size, making its phase structure characteristic become more prominent.\\nFig. 3 shows SEM images of the pure and 1% DIO-doped perovskite thin films. We observed that both samples show full coverage on the substrate with the absence of pinholes. The perovskite grain size appears to be significantly enlarged by the addition of DIO, increasing from an average value of 25.6 to 50.5 nm for control and DIO-modified samples, respectively, and there is an increase the crystallinity of the perovskite thin film. We note that the SEM imaging is only sensitive to the surface of the film. We presumed that the grains are predominantly propagating throughout the thickness of the film, but cannot exclude the possible presence of smaller crystallites at the buried interface.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 80,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Clevios PVP AI 4083 PEDOT:PSS was bought from Heraeus (Germany). CH3NH3I, PbCl2 (99.999%), and N,N-dimethyl formamide (DMF) (anhydrous, amine free; 99.9%) were purchased from Alfa-Aesar. PC61BM and Bphen were purchased from Nichem Fine Technology Co. Ltd. (Taiwan). CH3NH3I and PbCl2 were dissolved in DMF with a molar ratio of 3:1. The mixture was stirred at 60 \\u00b0C overnight in a glove-box.\\nThe synthesis of MoOx nanoparticles has been described elsewhere and the application of this material for highly efficient polymer solar cells has been reported by other groups. Molybdenum powder was purchased from Aladdin. First, 0.2 g of metal powder was dispersed in 20 ml ethanol with an ultra-sound bath. Then the solution was mixed with 0.7 ml hydrogen peroxide (30%). Ethanol was used to control the reaction rate between metal powders and hydrogen peroxide. During the reaction, ethanol will provide e\\u2212 and H+ for the reduction of the metal peroxide; meanwhile H+ can be inserted into the metal oxide lattice to form metal oxide bronzes. After 20 hours of reaction, molybdenum oxide solution turned from gray to blue, which is attributed to the H+ insertion into the metal oxide lattice and then the reduction of a metal element (Mo6+) to the sub-state (Mo5+), forming hydrogen molybdenum bronzes (HxMoO3). Finally, the remaining solvent was vaporized in a dry box, after which the obtained molybdenum bronze was dissolved in commercial PEDOT:PSS solution with different mixing ratios of 0.5 mg ml\\u22121, 1 mg ml\\u22121, and 1.5 mg ml\\u22121 respectively.\\n\\nDoped PEDOT:PSS films were obtained by spin-coating PEDOT:PSS with the MoOx dopant on a clear ITO surface under 4500 rpm/40 s and then annealing at 140 \\u00b0C for 20 min. For the perovskite layer, CH3NH3PbI3\\u2212xClx was spin coated from a dimethyl formamide (DMF) solution with CH3NH3I (synthesized in a previous study) and PbCl2 in a 3:1 molar ratio. The solution was spin-coated at 4000 rpm for 40 s in an N2 filled glovebox. The annealing of wet perovskite films was carried out by following a typical gradient increased temperature method, which can be found elsewhere. After drying at room temperature for \\u223c20 min, the samples were slowly heated from 50 \\u00b0C to 100 \\u00b0C at a ramp rate of 10 \\u00b0C/10 min on a hot plate. After that, 20 mg ml\\u22121 PC61BM in chlorobenzene was coated onto the perovskite layer at 2000 rpm for 40 s. Subsequently, the Bphen interfacial layer with 0.5 mg ml\\u22121 in ethanol was spin-coated without additional annealing. Ag (100 nm) was additionally deposited onto the Bphen layer under vacuum at 2 \\u00d7 106 Torr through a shadow mask, thus defining a device area of 7.25 mm2. The devices have a structure of ITO/PEDOT:PSS\\u2013MoOx/CH3NH3PbI3\\u2212xClx/PC61BM/Bphen/Ag (100 nm) (shown in Fig. 1b). Current density\\u2013voltage characteristics of PSCs under 1 sun illumination were measured under ambient conditions using a programmable Keithley 2400 source meter under AM 1.5G solar irradiation at 100 mW cm\\u22122 (Newport, Class AAA solar simulator, 94023A-U), and the characteristics have been described elsewhere. The incident-photon-to-current efficiency (IPCE) measurement was performed using a system combining a xenon lamp, a monochromator, a chopper and a lock-in amplifier together with a calibrated silicon photodetector. The distribution of MoOx in the PEODT:PSS film was investigated using a high-resolution scanning transmission electron microscope (JEM2200FS operating at 200 kV, JEOL).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Bphen,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 50,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0725,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2), cesium iodide (CsI), isopropanol (IPA), chlorobenzene (CB), o-DCB, toluene, dimethylsulfoxide (anhydrous, 99.8%), DMF, acetonitrile, Li-bis(trifluoromethanesulfonyl)imide (Li salt), and 4-tert-butylpyridine (tBP) were purchased from Sigma-Aldrich (USA). PC61BM, C60, and C70 were purchased from Nano-C Inc. (USA). Methylammonium iodide (MAI) and 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) were purchased from Xi\\u2019an Polymer Light Technology Corp. (China). Patterned ITO glasses and PTAA were purchased from Ying Kou You Xuan Trade Co., Ltd (China) and EM Index (Korea), respectively.\\n\\nC60 and C70 were dissolved in o-DCB, CB, and toluene with various weight ratios (ranging from 1:0 to 0:1) at 25 \\u00b0C under continuous stirring for 12 h. The solubility of C60 and C70 in each solvent was determined by filtering and weighing the sediment, which was completely dried under vacuum conditions for 3 h.\\n\\nThe PSCs were fabricated on ITO glass substrates with a configuration of ITO/PTAA/perovskite/ETL (PC61BM or C60:C70)/BCP/Ag, as shown in Fig. 1a. The ITO-coated glass substrates were cleaned sequentially with detergent, deionized water, and IPA and treated in an ultraviolet (UV)\\u2013ozone cleaner for 20 min. A PTAA solution was prepared by dissolving 10 mg of PTAA in 1 mL of toluene with the following additives: 7.5 \\u03bcL of a Li-salt solution in acetonitrile (170 mg mL\\u22121) and 4 \\u03bcL of tBP. The PTAA layer was formed by spin-coating the solution onto ITO glass at 3000 rpm for 30 s, followed by thermal annealing at 110 \\u00b0C for 10 min. The perovskite precursor solution was prepared by dissolving CsI, MAI, and PbI2 (molar ratio of 0.05:0.95:1) in anhydrous DMF to obtain a stoichiometric solution with a total concentration of 1.25 M, which was then stirred for 12 h at 60 \\u00b0C. The Cs0.05MA0.95PbI3 perovskite was formed by spin-coating the precursor solution onto the PTAA-coated samples at 4000 rpm for 30 s in an N2-filled glove box. During the spin-coating process, 200 \\u03bcL of CB (anti-solvent) was quickly dropped onto the samples at a delay time of 8 s. The samples were subsequently annealed on a hotplate at 100 \\u00b0C for 10 min. Next, 50 \\u03bcL of a PC61BM or FM solution with a concentration of 30.0 mg mL\\u22121 was spin-coated at 2000 rpm for 30 s to form the ETL. When the fullerene solubility of the ETL solution was <30.0 mg mL\\u22121, fullerene precipitates were formed in the solution. In this case, the precipitates were filtered out of the solution. Next, 70 \\u03bcL of a BCP solution (0.5 mg mL\\u22121 in IPA) was spin-coated onto the ETL at 4000 rpm. Finally, a 100 nm-thick Ag electrode was coated on top of the samples to form an effective working area of 0.1 cm2 (defined by a 0.2 cm-wide ITO bar and a 0.5 cm-wide Ag bar) using a thermal evaporator under high vacuum (<6.0 \\u00d7 10\\u22126 Torr).\\n\\nPhase images of the films in air were obtained using atomic force microscopy (AFM, Veeco, USA) in tapping mode. Top-view and cross-sectional scanning electron microscopy (SEM) images were obtained using a JSM-7500F field-emission scanning electron microscope (JEOL, Japan) at an acceleration voltage of 20 kV. The steady-state photoluminescence (PL) and time-resolved PL (TRPL) spectra were measured using a spectrometer (FLS920, Edinburgh Instruments, UK). The current density\\u2013voltage (J\\u2013V) characteristics of the PSCs were measured under an irradiation intensity of 100 mW cm\\u22122 (AM 1.5). The incident photon-to-electron conversion efficiency (IPCE) was measured using Solar Cell Scan 100 (Zolix, China). The space-charge-limited current (SCLC) of the electron-only device, i.e., ITO/Al/ETL (PC61BM or C60:C70/Al), was measured using a 2400 Source Meter in a dark environment with a bias voltage of 1 V. Electrochemical impedance spectroscopy (EIS) of the devices was performed in a dark environment using an electrochemical workstation (CH Instruments, USA). UV-visible (UV-vis) absorption spectra were recorded using a UV-vis-NIR 3600 spectrometer (Shimadzu, Japan). X-ray diffraction (XRD) measurements were measured by a Rigaku Smart Lab X-ray diffractometer (Japan) with Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5) at room temperature. Ultraviolet photoelectron spectroscopy (UPS) was performed with a Kratos Axis Ultra X-ray photoelectron spectroscope (Kratos Analytical, UK).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs0.05MA0.95PbI3,\\n Perovskite_composition_short_form: CsMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless mentioned otherwise, all materials and solvents were purchased from Youxuan Corp. and were used as received. N,N-Dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) were provided by Sigma-Aldrich, and methylammonium iodide (MAI) was provided by Xi'an Polymer Light Tech. The SnO2 colloid precursor was purchased from Alfa Aesar (tin(IV) oxide, 15% colloidal dispersion in H2O).\\n\\nITO glass substrates were cleaned in detergent aqueous solution and rinsed with deionized water three times, followed by sequential sonication in acetone and ethanol for 15 min each. After residual ethanol was evaporated, the substrates were further treated with UV-ozone for 15 min. A compact layer of SnO2 was deposited via spin-coating of diluted SnO2 aqueous solutions (SnO2 colloid precursor and deionized water, 1/6 v/v) at 4000 rpm for 20 s followed by annealing at 165 \\u00b0C for 30 min in air and UV-ozone treatment for 15 min. MAPbI3 films were prepared by spin-coating perovskite precursor solution (1.5 mol MAI and PbI2 in 1 ml mixed solvent of DMF and DMSO, 9:1 v/v) at 4000 rpm for 25 s and dropping 300 \\u03bcl antisolvent (DE or CBZ) \\u223c1 second before the turbid point. The perovskite films were then heated at 100 \\u00b0C for 5 min. To study the SCIC and observe the turbid point, no antisolvent was applied. After the spin-coating process, the perovskite films were heated at 100 \\u00b0C for 1 min. For the antisolvent with preheating, the perovskite precursor solution was diluted to 1.1 M, and both the chuck of the spin-coater and the SnO2 substrate were heated so that the substrate was spin-coated at the desired temperature. The chuck was made of aluminum and was directly heated by a hotplate without removing it from the spin-coater. After removing the hotplate, the temperature of the chuck was kept constant (within 5 \\u00b0C) over 60 s after a slight temperature decrease in the first 20 s, which was adequate to finish the deposition of the perovskite films at the designed preheating temperature (40 \\u00b0C or 70 \\u00b0C). After the MAPbI3 films were deposited, the hole-transporting material (HTM) layer was spin-coated from a solution consisting of 72.3 mg spiro-MeOTAD, 28.8 \\u03bcl 4-tert-butylpyridine, and 17.5 \\u03bcl Li-TFSI solution (520 mg Li-TFSI in 1 ml acetonitrile) in 1 ml of chlorobenzene. Finally, 80 nm of Au top electrode was thermally evaporated onto the HTM layer. All the materials were stored and all solutions were prepared in the glovebox. Fabrication of the PSCs was conducted in ambient air except for the deposition of the HTM layers, which were spin-coated in the glovebox. It should be noted that the humidity level of the spin-coating chamber was controlled by introducing humid air. The humid air was obtained by flowing air through a flask filled with water. Control of the flow of humid air yielded different relative humidity levels. A temperature/humidity meter was used to monitor the relative humidity and temperature inside the spin-coating chamber.\\n\\nTop-view SEM images of the perovskite films were obtained using an FEI-Inspect F50, Holland. X-ray patterns of the perovskite films deposited on SnO2 were obtained using an X-ray diffractometer (Bruker D8 Advance A25). UV-vis absorption spectra were recorded with an ultraviolet-visible (UV-vis) spectrophotometer (Shimadzu UV-3101 PC). Time-resolved PL measurements were carried out using a Rudower Chaussee 29 (PicoQuant GmbH). The exciting wavelength was 510 nm. J\\u2013V curves were recorded using a Keithley 2400 instrument under AM 1.5 G illumination (1000 W m\\u22122) from a solar simulator (Newport Oriel Solar 3 A Class AAA, 64023 A). The AM 1.5 G sunlight (100 mW cm\\u22122) was calibrated using a standard Si-solar cell (Oriel, VLSI Standards). The active area for the solar cells was 0.04 cm2. Metallographic microscopy was conducted using an MZ5000 instrument (Jiangnan Yongxin). Videos were taken using a portable camera (Huawei, V8). The external quantum efficiency (EQE) spectra were measured using a QTEST HIFINITY 5 (Crowntech).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The precursor solution in DMF, containing PbI2, PbCl2 and MAI with a molar ratio of 0.5:0.5:2, was spin-coated on PEDOT:PSS-covered FTO glass or pristine glass substrates at 3000 rpm for 60 s in a N2-filled glove box. Afterwards, the substrate was transferred onto a hotplate that was pre-heated to 100 \\u00b0C. A glass Petri dish at room temperature was used to cover the annealing film and a drop of pyridine (10 \\u03bcL) was immediately added to the Petri dish edge. Pyridine vapor would diffuse into the covered space, allowing the film to be annealed at 100 \\u00b0C within the pyridine vapor for 30 min. For the control sample that was prepared with the thermal annealing method, the film was annealed at 100 \\u00b0C for 30 min without being covered in a N2 atmosphere.\\n\\nThe solvent-annealed film on a PEDOT:PSS-covered FTO substrate was characterized using a FEI Quanta 400 F scanning electron microscope with a 10 keV accelerating voltage. For the transmission electron microscope characterization, the perovskite film was scratched off from the substrate and dispersed in toluene with strong sonication. Then, the dispersion (5 \\u03bcL) was dropped on a Cu mesh foil and baked dry. An electron beam with an energy of 120 keV was used in the TEM and SAED characterization. The perovskite film on the substrate was characterized with a Rigaku SmartLab X-ray diffractometer equipped with a Cu K\\u03b1 line radiation source at 40 kV, 40 mA. The diffraction patterns were collected with a step of 0.02\\u00b0 and a speed of 20\\u00b0 min\\u22121.\\n\\nThe perovskite films on glass substrates were characterized with a Hitachi U-3501 UV-visible absorption spectrometer and with a Hitachi F-7000 fluorescence spectrophotometer excited at a wavelength of 500 nm. For the charge carrier lifetime test, the same perovskite film was excited with a 532 nm laser at a powder density of 1 \\u03bcJ per cm2 per pulse. In order to characterize the microstructure and spatial distribution of the fluorescence properties, the perovskite film was tested using a Leica TCS SP5 confocal microscope excited with a 488 nm argon laser (single photon mode) or 960 nm pulsing Ti\\u2013sapphire laser (double photon mode), and the fluorescence signal was collected with a 750/50 nm band pass filter.\\n\\nSolar cells were fabricated based on the inverted-type planar structure, as represented by FTO/PEDOT:PSS/perovskite/PCBM/C60/BCP/Ag. Typically, the FTO glass substrate was washed in sequence with deionized water, iso-propanol and acetone with an ultrasonication bath. Before being used, the substrate was treated with microwave O2 plasma for 2 min. Then, the substrate was coated with 40 nm PEDOT:PSS by spin-coating Clevios AI 4083 aqueous solution at 4000 rpm, and heated on a hotplate at 150 \\u00b0C for 10 min in ambient conditions. The PEDOT:PSS-coated FTO substrate was transferred into a N2-filled glovebox to prepare the perovskite layer with the solvent annealing method, as described above. The thickness of the perovskite layer was characterized to be 350 nm by a Tencor \\u03b1-step 500 surface profiler and the cross-section-viewed SEM. Then, a layer of 100 nm-thick PCBM was covered on top of the perovskite layer by spin-coating at 1500 rpm, using 1,2-dichlorobenzene as the solvent with a concentration of 20 mg mL\\u22121. The films were further covered by C60 (20 nm) and BCP (10 nm) using a thermal evaporation method in a vacuum chamber at a pressure of 1 \\u00d7 104 Pa. Finally, a 100 nm-thick Ag layer was evaporated on top of the films in the same chamber. The active area of the device, as defined by the overlapping region between the Ag and the FTO electrodes, is 0.11 cm2.\\nThe solar cells were characterized under AM 1.5G illumination for the J\\u2013V response with a Keithley 2400 source meter unit at different scan speeds. The impedance spectroscopy of the solar cells was characterized with a Bio-logic SP-200 potentiostat/galvanostat/FRA, with a forward bias voltage ranging from 0.1 V to 0.8 V under illumination.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the materials and reagents were purchased from Sigma-Aldrich and used as received without further purification, unless otherwise mentioned. Spiro-OMeTAD was obtained from Merck Inc. CH3NH3I (99.8% purity) and tris [2-(1H-pyrazol-1-yl)-4-tert-butylpyridine] cobalt(III) tris[bis(trifluoromethylsulfonyl) imide] (FK209) (Co(III) complex FK209) were supplied by Dyesol Ltd.\\n\\nPatterned FTO glass (Pilkington TEC8, 8 \\u03a9 sq\\u22121) substrates were cleaned by the recipe described elsewhere. After a 15 min UV-ozone treatment for further cleaning, the precursor films of Fe2O3 ETLs were spin-coated on pre-cleaned FTO substrates using the solution of 0.404 g Fe(NO3)3\\u00b79H2O and 10 \\u03bcL TiCl3 (CAS: 7705-07-9, Sigma-Aldrich) dissolved in 10 mL ethanol. After being sintered at 550 \\u00b0C for 60 min in a muffle furnace, the samples were taken out directly from the furnace and quenched quickly to room temperature from 550, 450, and 350 \\u00b0C, respectively. Thus, the Fe2O3 ETLs with non-equilibrium Ti4+ dopants were obtained, and labeled as quenched Ti-Fe2O3. The sample cooled naturally was also prepared for comparison, which was marked as normal Ti-Fe2O3. All samples were finally transferred to a glovebox for cell fabrication.\\n\\nCH3NH3PbI3 film was deposited on Ti-Fe2O3 ETLs by a Lewis base adduct-based one-step spin-coating method proposed by Park et al., which was slightly modified with a face-down annealing recipe proposed in our previous work to form a (110) texture in the films. In detail, a 50 \\u03bcL precursor containing of 79.5 mg CH3NH3I, 230.5 mg PbI2, 39 mg anhydrous dimethyl sulfoxide (DMSO), and 300 mg anhydrous N,N-dimethylformamide (DMF) was added dropwise on the Ti-Fe2O3 ETL, which was spun subsequently at 4500 rpm for 30 s. After the first 6 s of the spinning process, 500 \\u03bcL of diethyl ether was added dropwise on it by means of an injection syringe. After that, the sample was placed face-up on a hot plate with a preset temperature of 40 \\u00b0C for 30 s. Subsequently, the film was turned face-down and annealed at a constant temperature of 100 \\u00b0C for about 15 min to enable a full crystallization of CH3NH3PbI3 film.\\nTo complete the solar cell fabrication, a 100 nm hole transporting layer was coated on CH3NH3PbI3 film by spin-coating 100 \\u03bcL premixed precursor solution at 3000 rpm for 30 s. The solution contains 72.5 mg spiro-MeOTAD, 28 \\u03bcL 4-tertbutylpyridine, 17.5 \\u03bcL Li-TFSI in acetonitrile, 75 \\u03bcL Co(III) complex FK209/acetonitrile solution (7.5 mM), and 1 mL chlorobenzene. After being stored in a humidity-controlled dark environment for 10 h, an Ag counter electrode with a thickness of about 100 nm and a specific area of 0.28 cm2 was finally coated on a hole transporting layer via vacuum thermal evaporation.\\n\\nThe cells were without any encapsulation, and all the measurements of PV features were conducted at room temperature under ambient conditions. The J\\u2013V curves were tested by use of a Keithley 2400 source meter under standard AM 1.5 G simulated illumination (100 mW cm\\u22122, XES-70S1). A shadow mask with a specific hole area of 0.09 cm2 was adopted to define the active area of the cell. EQE curves were measured by means of a commercialized quantum efficiency measurement system (SCS10-X150, Zolix Instrument Co. Ltd). The EQE data were collected under DC mode without any bias light. The stabilized power output of the cell was tested by applying a constant voltage, which refers to its maximum power point in the J\\u2013V curve. A standard Newport silicon solar cell was adopted to calibrate all the illumination systems.\\nXPS measurements were taken on a photoelectron spectrometer (PHI-5702) using Al K\\u03b1 monochromatic radiation. To investigate the bulk elemental composition of Ti-Fe2O3 ETLs, the samples were etched by argon ions (2 keV, \\u223c50 \\u03bcA cm\\u22122) for 60 s at a chamber vacuum of 5 \\u00d7 10\\u22123 Pa. The data were calibrated with the binding energy of a C 1s peak at 284.6 eV to relieve any charging effects. M\\u2013S measurements were performed in 1.0 M NaOH on an electrochemical analyzer (Princeton Applied Research, 2273) at a frequency of 1000 Hz under dark conditions, using a 10 mV amplitude sinusoidal perturbation. Raman spectra were collected on a Renishaw RM-1000 laser Raman microscopy system. Absorption properties of the samples were studied using a PerkinElmer Lambda 950 spectrophotometer. SEM images were taken on a Zeiss Supra-40 Field-Emission SEM. AFM images were obtained by means of a Veeco NanoScope IV Multi-Mode AFM. XRD patterns were measured using a Rigaku Ultima III X-ray diffractometer system. The patterns were collected in the range of 10\\u201360\\u00b0 with a scan speed of 10\\u00b0 min\\u22121. PL spectra were tested on a fluorescence spectrophotometer (Hitachi F-7000 spectrophotometer) at room temperature with an excitation wavelength of 515 nm. TRPL curves were recorded using a time-correlated single-photon counting technique (Picoharp 300) under a 505 nm laser beam pulse with a frequency of 5 MHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: Fe2O3,\\n ETL_additives_compounds: Ti,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 40; 100,\\n Perovskite_deposition_thermal_annealing_time: 0.5; 15.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All reagents were used as received without further purification. PbI2 and spiro-OMeTAD were obtained from Merck KGaA. Lithium bis(trifluoromethane) sulfonimide salt (Li-TSFI, 99.95%), Tetrahydrofuran (THF) and chlorobenzene were purchased from Alfa Aesar. Titanium(IV) isopropoxide (99.999%) was purchased from Aldrich. Methylamine ethanol solution (30 wt%, ME) and 4-tert-butylpyridine (TBP) were the products of Aladdin. CH3NH3I was prepared according to a reported procedure.\\nTo prepare MAPbI3 crystals, CH3NH3I and PbI2 were mixed and dissolved in GBL (1.23 M) as the precursor solution, and after the solution was heated at 100 \\u00b0C for 24 h, plenty of small crystals were formed. The above crystallization process was carried out in a fresh precursor solution with the small crystals as seeds. Large crystals were collected after for 24 h.\\nThe MAPbI3 solutions in TME were prepared by dissolving a certain amount of MAPbI3 crystals in TME with different volume ratios of THF:ME, under ultrasonic treatment at the ambient temperature. The practical concentration was then determined from the practical volume of the solution.\\n\\nThe solution of MAPbI3 in TME (0.6 M) was deposited onto the mesoporous TiO2/FTO glass substrate (300 mm \\u00d7 400 mm), and was coated by a home-built blade-coater at a constant rate of 150 mm s\\u22121. The distance between the blade and the substrate was 0.3 mm. The MAPbI3 films were obtained after the solution was dried at room temperature.\\n\\nFluorine-doped Tin Oxide (FTO) glass substrates with a dimension of 2.5 cm \\u00d7 2.5 cm were patterned by laser etching. The substrates were sequentially washed in ultrasonic baths of acetone, distilled water and ethanol, and then dried with high-purity nitrogen flow. A 10 min ultraviolet-ozone treatment was performed before device fabrication to eliminate the residual organic contaminant on the substrates. To fabricate compact TiO2 layers, 1 mL titanium(IV) isopropoxide was mixed with 5 mL 2-methoxyethanol and 0.5 mL ethanolamine to prepare the precursor solution, which was then stirred at 80 \\u00b0C for 2 h and coated on FTO glass by spin-coating under 3000 rpm for 30 s in air. The substrate was dried on a hot plate at 120 \\u00b0C for 10 min, and then annealed at 500 \\u00b0C for 30 min. After cooling to room temperature, a \\u223c300 nm thick mesoporous TiO2 film was deposited on the compact TiO2 layer by spin-coating of the TiO2 paste (Dyesol DSL18NR-T) with ethanol (1:5, mass ratio), followed by heating at 500 \\u00b0C for 30 min. The MAPbI3 solution in TME was then spin-coated onto the TiO2-covered substrate at 2000 rpm for 30 s to fabricate the MAPbI3 layer. The HTL layer was deposited on the MAPbI3 film by spin-coating the spiro-OMeTAD solution (80 mg mL\\u22121 containing 17.5 \\u03bcL Li-TFSI/acetonitrile (520 mg mL\\u22121) and 28.5 \\u03bcL TBP) at 3000 rpm for 30 s. Finally, 10 nm MoO3 and 100 nm Ag were thermally evaporated under a pressure of 1 \\u00d7 10\\u22127 mbar. All device fabrication steps and measurement were carried out in an N2-purged glove box (<0.1 ppm O2 and H2O).\\nFor the 10 cm2 module, each layer was deposited following the same procedure as described above except that laser scribing patterning processes were used to separate individual cells and construct the series electrical connection. As shown in Fig. 5E, the FTO substrate was first divided into sub-cells with a 1064 nm laser (P1). After deposition of MoO3 and prior to deposition of the top electrode, 532 nm laser scribing was employed to etch the MAPbI3 layer and expose the bottom electrode of the neighbor sub-cell (P2). The module was completed by dividing the module by 532 nm laser scribing (P3).\\n\\nApparent viscosity was measured on an ARES-G2 rheometer (TA Instruments, US). Optical microscopic images were obtained using a BX53 polarizing microscope (Olympus, Japan) equipped with a DXM1200 charge-coupled device (CCD) camera (Nikon, Japan). SEM images were recorded on a SU-70 scanning electron microscope (Hitachi, Japan). Steady fluorescence spectra were recorded on a Fluoromax 4 spectrometer (HORIBA, Japan) with excitation at 520 nm. The time-resolved fluorescence spectra were measured on an FLS980 spectrometer (Edinburgh Instruments, UK), with peak emission at 780 nm. UV-Vis spectra measurements were performed using a UV-2700 spectrophotometer (Shimadzu, Japan). DLS measurements were carried out on a Nano ZS Zetasizer (Malvern, UK). J\\u2013V measurement of the solar cells was performed using a Keithley 2400 source meter and 300 W collimated xenon lamp (Newport) calibrated with the light intensity to 100 mW cm\\u22122 under simulated AM 1.5G illumination by a certified silicon solar cell. IPCE was measured on a computer-controlled IPCE system (Newport) containing a xenon lamp, a monochromator, and a Keithley multimeter. The system was calibrated with a certified silicon solar cell and the IPCE data were collected in the DC mode. All the above measurements were carried out at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Methanol; THF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Ethanol and 1-butanol were purchased from Dychemi and Tokyo Chemical Industry. Spiro-MeOTAD and PbI2 were obtained from the Luminescence Technology Corp. and Fisher Scientific, respectively. In addition, the TiO2 paste was purchased from Dyesol and diluted with ethanol before use. All other materials were purchased from Sigma-Aldrich and were used in the as received condition. Furthermore, CH3NH3I (MAI) was synthesized via a previously described method.\\n\\nAnatase TiO2 nanoparticles were purchased as TiO2 paste (18NR-T, average size \\u223c20 nm) from Dyesol. The spray solution was prepared in the same manner as the spin-coating precursor. The TiO2 paste was mixed with anhydrous ethanol to form a 1:5.5 wt% mixture. In addition, a syringe pump was used to inject the precursor solution into a 25 gauge nozzle at flow rates ranging from 0.1 mL h\\u22121 to 0.5 mL h\\u22121. A high voltage (6\\u201310 kV) was applied between the needle tip and the plate by using a direct current (dc) power supply; the distance between the needle tip and the plate was fixed at 5 cm.\\n\\nThe solar cells were fabricated on glass/FTO substrates (Pilkington, TEC8), which were washed for 10 min each with acetone, ethyl alcohol, and deionized water, in an ultrasonic bath. Furthermore, perovskite solar cells were prepared via the solvent engineering method. This was done by first spin-coating a dense, hole blocking layer of TiO2 (bl-TiO2, \\u223c80 nm-thick) from 0.15 M and 0.3 M titanium diisopropoxide bis(acetylacetonate) in 1-butanol solution, which was heated at 125 \\u00b0C for 5 min. Moreover, mesoporous TiO2 (mp-TiO2, \\u223c200 nm-thick) was prepared by the spin-coating or spraying of the diluted TiO2 paste in ethanol, and heating at 80 \\u00b0C for 10 min. The substrates were then annealed at 500 \\u00b0C for 1 h. A portion (46 wt%) of methylammonium lead tri-iodide (CH3NH3PbI3) solution was prepared by mixing a 1:1 molar ratio of MAI and PbI2 powder into a mixture of GBL and DMSO (7:3 v/v). The resulting mixture solution was stirred at 70 \\u00b0C for 1 h, and then spin-coated onto the mp-TiO2/bl-TiO2/FTO substrate via the, previously mentioned, solvent engineering method. A smooth and uniform 200\\u2013300 nm CH3NH3PbI3 light-absorbent layer was fabricated in a two-step spin-coating process performed at 1000 and 5000 rpm for 10 and 20 s, respectively; toluene was dripped during the second step. After drying at 100 \\u00b0C for 10 min, 25 \\u00b5L of the hole transport layer (72 mg of 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenyl-amine)-9,9\\u2032-spirobifluorene) (Spiro-MeOTAD), 28.8 \\u00b5L of 4-tert-butylpyridine, and 17.2 \\u00b5L of bis(trifluoromethane)sulfonamide lithium salt (Li-TFSI) solution (720 mg mL\\u22121 in acetonitrile) (the entire mixture was dissolved in 1 mL of chlorobenzene) were formed after spin coating at 3000 rpm for 30 s. The processes were all conducted inside a glovebox (Korea Kiyeon), under controlled atmospheric conditions and at a humidity of <0.5 ppm. Moreover, a 50 nm-thick Au electrode was deposited at \\u223c10\\u22126 bar via thermal evaporation.\\n\\nPlanar SEM and cross-sectional images of the perovskite solar cell structure were obtained via field-emission scanning electron microscopy (FESEM, AURIGA, Carl Zeiss), combined with a focused ion beam system (FIB system, AURIGA, Carl Zeiss). XRD spectra of the mesoporous TiO2 layer prepared by ESD and spin-coating were recorded by using a glazing incidence X-ray diffractometer (New D8 advance, Bruker). The current\\u2013voltage characteristics were determined and impedance spectroscopy measurements of the solar cells were performed using a solar simulator (Newport Oriel Solar 3A Class AAA, 64023A) and a potentiostat (CHI 600D, CH instruments); the measurements were conducted under an illumination of AM 1.5G sun (100 mA cm\\u22122), and the potentiostat was calibrated using a standard Si-solar cell (Oriel, VLSI standards) and a light sensor current controller (Newport Oriel digital exposure controller, Model 68945). All devices were measured by masking the active area with a thin mask (0.14 cm2) to reduce the scattered light. J\\u2013V characteristics for all devices were measured at a voltage scan rate of 0.05 V s\\u22121.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.14,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Spiro-OMeTAD, PbI2, 4-tert-butylpyridine (TBP) and MAI were purchased from Xi'an Polymer Light Technology Corp. The FTO substrates were cleaned with deionized water and ethanol. The blocking layer was spin-coated a 0.15 M solution of titanium diisopropoxidebis (acetylacetonate) (75 wt% in isopropanol, Aldrich) in 1-butanol at 2000 r.p.m. for 50 s and dried at 125 \\u00b0C for 10 min. The mesoporous TiO2 (mp-TiO2) was spin-coated TiO2 paste (Dyesol, 18NR-T) diluted in anhydrous ethanol (2:7, weight ratio) at 3000 r.p.m. for 30 s and then annealed at 500 \\u00b0C for 30 min. The perovskite was deposited onto mp-TiO2 by spin-coating 1.0 mM MAPbI3 precursor solution with 3000 r.p.m. for 55 s. At the remaining spin time of 49 s, 100.0 \\u03bcL DRM antisolvent was quickly added onto MAPbI3 film (DRM1: 2 \\u03bcL DMSO and 98 \\u03bcL CB, DRM2: 4 \\u03bcL DMSO and 96 \\u03bcL CB and DRM3: 6 \\u03bcL DMSO and 94 \\u03bcL CB). Here 100.0 \\u03bcL CB antisolvent was used as a control-experiment. The substrates were annealed at 100 \\u00b0C for 10 min after the whole process of spin-coating. The Spiro-OMeTAD film was prepared by spin-coating a solution that 72.3 mg Spiro-OMeTAD, 28.8 \\u03bcL TBP and 17.5 \\u03bcL of a stock solution of 520.0 mg mL\\u22121 lithium bis(trifluoromethylsulphonyl)imide in acetonitrile in 1.0 mL CB at 3000 r.p.m. for 30 s. Eventually, 80 nm of gold was thermally evaporated on the film to form the back contact.\\n\\nScanning electron microscope (SEM) images were performed with a JEOL JSM-7600F device. Absorption spectra were determined with SHIMADZU ultraviolet to visible spectrophotometer. The X-ray diffraction (XRD) analysis was characterized by a D1 Evolation using Cu Ka radiation at a coincident scan rate of 6\\u00b0 min\\u22121. The current-voltage (J-V) characteristics were measured with a fixed active area of 0.09 cm2 using a CH Instruments 660C electrochemical workstation (Shanghai CH Instruments Co., China) under AM 1.5G illumination (100 mW cm\\u22122) provided by a short-arc xenon lamp (CHF-XW-500W, Trusttech Co. Ltd., China). The incident photo-to-current conversion efficiency (IPCE) was obtained by Qtest Station 2000 IPCE Measurement System. The steady-state photoluminescence (PL) spectra were measured using an integrated Raman system (Horiba JY HR800) with an Olympus 15X NUV lens (NA = 0.32). A 325 nm helium-cadmium (He-Cd) laser was used as the excitation source. The laser power density on the film surface was about 2 W cm\\u22122 and the wavelength scale was from 500 to 900 nm. Electrochemical impedance spectroscopy (EIS) were tested using a CH Instruments 660 C electrochemical workstation (Shanghai CH Instruments Co., China) with a 20 mV amplitude over a frequency range of 10\\u22121 Hz to 105 Hz under dark condition and the Init E (mV) was \\u2212300 mV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbS QDs were synthesized on the basis of a published method [36]. Briefly, 106\\u202fmg of sulfur powders was added in 4\\u202fmL of oleylamine (OLA) with stirring at 40\\u202f\\u00b0C for 0.5\\u202fh. Meanwhile, 0.36\\u202fg of lead oxide (PbO), 1\\u202fmL of oleic acid (OA) and 15\\u202fmL of 1-octadecene (1-ODE) were mixed, stirred, and heated to 145\\u202f\\u00b0C under nitrogen atmosphere for 1\\u202fh. Afterwards, 2\\u202fmL of solution of sulfur in OLA was injected into the PbO solution. The temperature was reset to 100\\u202f\\u00b0C, and heated for 10\\u202fmin. Subsequently, the QDs were purified and extracted. Finally, the PbS QDs were dispersed in hexane with different concentrations (0.5, 1.0 and 1.5\\u202fmg\\u202fmL\\u22121).\\n\\nFluorine-doped tin oxide (FTO) glass substrate was cleaned in succession with deionized water, ethanol and acetone by ultrasonication for 15\\u202fmin each. After dried in oven at 80\\u202f\\u00b0C, the substrate was further cleaned in ultraviolet-ozone for 15\\u202fmin. Then, the TiO2 blocking layer (bl-TiO2) was deposited on the FTO glass by spin-coating according to the reported method [39]. The PSK precursor solution was prepared by dissolving 0.484\\u202fg of PbI2 and 0.159\\u202fg of CH3NH3I in DMF/DMSO mixed solution (4:1 v/v) and stirring at 60\\u202f\\u00b0C for 1\\u202fh. The solution was spin-coated on the FTO/TiO2 substrate at 4000\\u202frpm for 30\\u202fs, and 200\\u202f\\u03bcL of toluene was dropped on the substrate at 5\\u202fs. Then, the substrate was annealed at 100\\u202f\\u00b0C for 10\\u202fmin. Different concentrations of PbS QDs were dynamically spin-coated on PSK film at 2000\\u202frpm for 30\\u202fs. After heating for 2\\u202fmin in 100\\u202f\\u00b0C, Spiro-OMeTAD solution (74\\u202fmg of Spiro-OMeTAD dissolved in 1\\u202fmL of chlorobenzene with the addition of 28.8\\u202f\\u03bcL of TBP and 17\\u202f\\u03bcL of Li-TFSI/acetonitrile (520\\u202fmg\\u202fmL\\u22121)) was deposited on PSK/PbS film by spin-coating at 3000\\u202frpm for 30\\u202fs. By contrast, the pristine sample was spin-coated the Spiro-OMeTAD without the PbS QDs layer. Finally, a 50\\u202fnm-thick counter electrode (Au) was deposited on Spiro-OMeTAD layer by thermal evaporation.\\n\\nUV\\u2013vis absorption analysis of PbS QDs in hexane dispersion was performed by UV\\u2013vis spectrophotometer (Lambda 750 S, PerkinElmer, USA). Electronic images of PbS QDs, PSK films and PSCs were collected by high-resolution transmission electron microscope (HRTEM, Titan G2, FEI, USA) and JSM-7500F field emission scanning electron microscope (FESEM, JEOL, Japan). Contact potential differences (CPDs) were measured via a gold probe (3\\u202fmm diameter, Instytut Fotonowy, Poland) as the reference and a Kelvin control (Instytut Fotonowy, Poland) with a sensitivity of 1\\u202fmV and 460\\u202fnm excitation light on the indium-doped tin oxide (ITO) glass substrates. The surface of PSK films was evaluated by a multimode 8 atomic force microscope (AFM, Bruker, USA) in Scan Analyst mode. The contact angles were obtained from contact angle meters (Theta Lite, Blolin, Finland). X-ray diffraction (XRD) patterns were obtained by a D/MAX-RB X-ray diffractometer (Rigaku, Japan). UV\\u2013vis absorption spectra of the PSK films were measured by a UV\\u2013visible spectrometer (UV2600, Shimadzu, Japan). Steady-state photoluminescence (PL) spectra were acquired by a fluorescence spectrophotometer (F-7000, Hitachi, Japan) with 460\\u202fnm excitation wavelength. Photocurrent-voltage (J-V) characteristics and electrochemical impedance spectroscopy (EIS) were recorded by an electrochemical work station (CHI660C, Chenhua Instrument Crop., China). The J-V characteristics were measured under an illumination of 1 sun (100\\u202fmW\\u202fcm\\u22122, AM 1.5G) generated by a solar simulator (91160, Newport Corp., USA) and the active cell area was 0.09\\u202fcm2. The EIS was measured at dark under the bias of 0\\u202fV in the frequency range of 0.01\\u2013105\\u202fHz. The incident monochromatic photoelectric conversion efficiency (IPCE) was tested using Newport's QE/IPCE Measurement Kit with monochromatic light from a 300\\u202fW Xe lamp (Newport, model no. 6258).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"MAI was synthesized by a mixed solution of 27 mL methylamine and 30 mL HI (57 wt% in water) at 0 \\u00b0C and stirred for 2 h. The precipitate was recovered at 50 \\u00b0C for 1 h. The product was washed with diethyl ether until becoming white colour and dried at 60 \\u00b0C in a vacuum oven for 18 h. Formamidine acetate (3 g) and hydroiodic acid (13 ml) were mixed at 0 \\u00b0C and stirred for 2 h. The solvent was removed by rotary evaporation. The product was washed with diethyl ether three times, followed by recrystallization with ethanol and finally dried at 60 \\u00b0C in a vacuum oven.\\n\\nDevices were fabricated on fluorine-doped tin oxide (FTO) coated glass, Initially FTO was removed by etching the FTO with 2 M HCl and zinc powder. Substrates were then ultrasounded sequentially in hallmanex detergent, acetone, and ethanol. A \\u223c100 nm compact layer of TiO2 was subsequently deposited by spin-coating method with a precursor solution of 0.15 M titanium diisopropoxide bis(acetylacetonate) (75 wt% in isopropanol) in 1-butanol (99.8%) at 3000 rpm and heated at 150 \\u00b0C for 10 min. A 500 nm mesoporous TiO2 layer was spin-coated on the substrate and sintered at 500 \\u00b0C for 30 min. The samples were then submerged in a 15 mM aqueous TiCl4 bath at 70 \\u00b0C for 30 min, followed by rinsing with deionized water and annealed at 500 \\u00b0C for 30 min. The MAPbI3 and FAxMA1-xPbI3 were deposited into the porous films by a two-step sequential method. First, a mixed solution of PbI2 (1.2 M) and PbCl2 (0.2 M) in N,N-dimethylformamide (DMF) was spin-coated on a simple TiO2 film before loading MAI or FAxMA1-xI (both the concentrations are 0.044 M) solution to synthesize high-quality perovskite layer, followed by a heating treatment at 100 \\u00b0C for 10 min. Carbon pastes with and without MAI were sequentially doctor bladed onto the perovskite loaded substrate after the samples cooled.\\n\\nExternal potential bias to the device under simulated illumination (Newport, 91192) provided the current-voltage characteristics of the cells with a power density of 100 mW cm\\u22122. The power of the simulated light was adjusted to be 100 mW cm\\u22122 by a standard silicon cell (Newport Corporation, Irvine, CA). The incident photon conversion efficiency (IPCE) measurements on PSC were performed using a 300 W xenon lamp (Newport, 66984) ranging from 300 to 850 nm in wavelength. Optical features of these Samples were characterized by UV\\u2013vis spectrophotometry (Lambda 950, PerkinElmer). The surface morphologies of these samples were observed by scanning electron microscopy (SEM, Sirion FEG, USA). X-ray diffraction (XRD) measurements were performed on a D8 Focus diffractometer with Cu Ka radiation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | TiCl4,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 10.0,\\n HTL_stack_sequence: none,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Unknown,\\n Backcontact_stack_sequence: Carbon,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Doctor blading,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The 2D and 3D perovskites were prepared through changing the organic molecules between the inorganic layer and the organic spacer molecules, i.e. benzylamine and methylammonium for the 2D and 3D perovskites, respectively. A 100 mL two-necked round-bottom flask was charged with 10 mL of HI (57% aq., 1.5% H3PO2) and a stir bar. The solution was degassed with nitrogen for 1 min, and the flask was kept in nitrogen for the duration of the experiment. The flask was heated to 100 \\u00b0C in an oil bath while stirring, at which point lead iodide (PbI2, 1.383 g, 3 mmol) was added and then the mixture was stirred vigorously to dissolve the lead iodide; this resulted in a translucent bright yellow solution. The flask was heated to 120 \\u00b0C, at which point benzylamine hydrochloride (0.287 g, 6 mmol) and methylamine hydrochloride (0.405 g, 6 mmol) were added according to the dimensional perovskite. After adding the organic molecules, the heat was turned off, the flask was removed, and it was allowed to cool to room temperature. Once cool, the solution was filtered and then dried at 50 \\u00b0C for 24 h.\\n\\nThe N-type TiO2 layer was formed using the following method. A 50 nm TiO2 blocking layer (TiO2 BL) was deposited on the FTO substrate via spin coating (2000 rpm, 30 s) a mildly acidic solution of titanium isopropoxide (TTIP) in ethanol (350 \\u03bcL TTIP in 5 mL EtOH containing 0.013 M HCl), and then the sintering process was conducted at 550 \\u00b0C for 30 min. A mesoporous TiO2 layer was spin-coated on the TiO2 compact layer with a diluted TiO2 paste (DYESOL-30NRD) with ethanol at a ratio of 1:3.5 w/w at 500 rpm for 5 s, 3000 rpm for 10 s, and 6000 rpm for 30 s. The substrate was further treated with 20 mM TiCl4 aqueous solution at 70 \\u00b0C for 30 min, rinsed with deionized water and ethanol, and then sintered at 500 \\u00b0C for 30 min. Next, 30 wt% BAPbI4 perovskites were dissolved in the DMF solvent. The solution was spin-coated on the N-type TiO2 layer at 4000 rpm for 30 s followed by an annealing process at 100 \\u00b0C for 1 min in order to eliminate residual solvents. Subsequently, the lab-made CH3NH3I powder was dispersed around the cooled BAPbI4 film on a hot plate as described in the literature . The sample was covered with a glass container and annealed at 160 \\u00b0C from 30 s to 7 min.\\nTo fabricate the 3D CH3NH3PbI3 peovskite device, a 40 wt% precursor solution of PbI2 and MAI (molar ratio 1:1) in DMF was made and then, spin-coated on the TiO2 mesoporous layer at 6000 rpm for 30 s. The film was annealed at 100 \\u00b0C for 10 min. The hole transporting layer was prepared according to the literature . A solution for the spiro-MeOTAD coating was prepared through dissolving 72.3 mg spiro-MeOTAD in 1 mL of chlorobenzene, to which 28.8 \\u03bcL of 4-tert-butyl pyridine and 17.5 \\u03bcL of lithium bis(trifluoromethanesulfony) imide solution (520 mg Li-TSFI in 1 mL acetonitrile) were added. The spiro-MeOTAD was deposited on the perovskite layer at 4000 rpm for 30 s. For the counter electrode, a gold layer of 800 \\u00c5 was deposited on the perovskite layer with the thermal evaporation at 1 \\u00c5 s\\u22121.\\n\\nThe photocurrent (Jsc) and photovoltage (Voc) of the solar cell were measured with an active area of 0.2 cm2 using simulated solar light at AM 1.5G produced by a 1000 W xenon lamp (Oriel, 91193). Its irradiant power was adjusted according to a Si reference solar cell (Fraunhofer Institute for Solar Energy System: Mono-Si + KG filter) to have approximately one-sun light intensity (100 mW/cm2). The incident photon-to-current efficiency (IPCE) was measured using a system designed using the photovoltaic measurement. A 12 W halogen lamp was applied as a light source for the monochromatic beam. For its calibration, a silicon photodiode (NIST-calibrated photodiode G425) was used. The IPCE data were obtained at a low chopping speed of 5 Hz, and the quantum efficiency was detected using a lock-in amplifier. The electrochemical impedance spectroscopy (EIS) data were obtained under one sun illumination using a potentiostat (Solartron 1287) equipped with a frequency response analyzer (Solartron 1260) under a frequency ranging from 10\\u22122 to 106 Hz.\\nThe intensity modulated photovoltage spectroscopy (IMVS) and intensity modulated photocurrent spectroscopy (IMPS) measurements were performed on a ZAHNER CIMPS system. The LED was operated using a potentiostatic feedback loop to control the stationary DC voltage and a concurrent sinusoidal modulated AC voltage. The AC amplitude was determined from 10% of the stationary DC value. The transfer functions of IMPS and IMVS were operated by the system response to the stimulation signal. The solar cell was placed under the potentiostat unit. The IMPS and IMVS were measured under short circuit and open circuit conditions, respectively. The short circuit photocurrent efficiency (\\u03a6ext(\\u03c9)) of the IMPS and the real and imaginary parts of the modulated photovoltage (\\u0394Voc) of the IMVS were calculated using the Levenberg-Marquardt algorithm.\\n\\nCrystals of MAPbI3 and BAPbI4 were coated with paratone-N oil, and the diffraction data were measured at 298 K with synchrotron radiation (\\u03bb = 0.61000 \\u00c5) on an ADSC Quantum-210 detector at BL2D SMC with a silicon (111) double crystal monochromator (DCM) at the Pohang Accelerator Laboratory, Korea. The PAL BL2D-SMDC program was used to collect the data (detector distance = 63 mm; omega scan, \\u0394\\u03c9 = 3\\u00b0; exposure time = 1 s/frame) and HKL3000sm (Ver. 703r) was used for the cell refinement, reduction, and absorption correction. The crystal structures of MAPbI3 and BAPbI4 were solved using the direct method with the SHELXT-2014/5 program , and they were refined using the full-matrix least-squares calculations in the SHELXL-2014/7 program .\\n\\nThe scanning electron microscopy (SEM) images of the perovskite morphology were obtained using a field emission scanning electron microscope (FE-SEM, Sirion, The Netherlands). The X-ray diffraction (XRD) patterns were measured using a D8 Discover thin-film diffractometer with Cu K\\u03b1 radiation (40 kV, 30 mA, \\u03bb = 1.54056 \\u00c5) and a Ni filter plus a graphite monochromator. The XRD spectrum was recorded in a Bragg-Brentano configuration using \\u03b8/2\\u03b8 scanning and no tilt angle. The field-emission transmission electron microscopy (FE-TEM) images were obtained using a JEM-2100F (JEOL Ltd., Japan). The diffuse reflectance spectra of the perovskites were measured with an ultraviolet-visible-near infrared (UV-Vis-NIR) spectrophotometer (Cary 5000, Varian). The emission and exciton spectrum of BAPbI4 were measured with a FluoroMate FS-2 Fluorescence Spectrometer (Scinco, Republic of Korea). The fluorescence lifetime imaging (FLIM) was measured using an inverted scanning confocal microscope (MicroTime-200, Picoquant, Germany; Korea Basic Science Institute (KBSI) Daegu Center) with a 40 x (air) objective. A single-mode pulsed diode laser (470 nm with an IRF of approximately 30 ps and an average power of < 0.3 \\u03bcW) was used as the excitation source. A dichroic mirror (490 DCXR, AHF), a long-pass filter (HQ500lp, AHF), a 75 \\u03bcm pinhole, a band-pass filter, and a single photon avalanche diode (PDM series, MPD) were used to collect emissions from the samples. The time-correlated single-photon counting (TCSPC) technique was used to count the fluorescence photons. The FLIM images, which were 200 \\u00d7 200 pixels, were recorded using the time-tagged time-resolved (TTTR) data acquisition method. The acquisition time of each pixel was 1 ms. Exponential fittings for the obtained fluorescence decays, which were extracted from the FLIM images, were performed using the Symphotime software (version 5.3).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | TiCl4,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.2,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium isopropoxide (99.999%), lithium bis(trifluoromethylsulfonyl)-imide (Li-TFSI, 99.95%) were achieved from Sigma-Aldrich. 18NR-T, CH3NH3I (99.5%), PbI2 (99.99%), Spiro-OMeTAD (99.5%) and tertbutylpyridine (tBP, 96%) were purchased from Xi'an Polymer Light Technology Corp. The tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) bis(trifluoromethylsulphonyl) imide (FK209, 99%) was purchased from Shanghai MaterWin New Materials Co., Ltd. The compounds LHTM-1 and LHTM-2 were prepared according to the previous report methods of our group . All other solvents and chemicals obtained from commercial sources and used as received without further purification.\\n\\nThe compact TiO2 layer solution was prepared according to following method already reported by our group : 369 \\u03bcL of titanium isopropoxide was added into 2.53 mL of ethanol, and simultaneously 35 \\u03bcL of 2 M HCl solution was added into 2.53 mL of ethanol in another vial. The second solution was then added dropwise to the first solution with fierce stirring. The resulting solution was clear and transparent and was immediately discarded if cloudy. The mixture was filtered with a 0.22 \\u03bcm filter. The perovskite precursor solution was prepared by mixing 1.2 mmol PbI2 and 1.2 mmol CH3NH3I in 1 mL of N,N-dimethylformamide (DMF) and was stirred at 60 \\u00b0C for 12 h. LHTM-1 and LHTM-2 were dissolved in chlorobenzene, Li-TFSI, tBP and FK209 were added to the HTM solutions as dopants. As the comparison, the Li-TFSI, tBP doped Spiro-MeOTAD solution were prepared. The HTM solutions were stirred over night.\\n\\nFluorine-doped tinoxide (FTO) substrates were sequentially cleaned by ultrasonic bath with a solution of detergent diluted in deionized water, alkaline ethanol solution, ethanol, acetone and deionized water, each cleaning step lasted for 30 min and then dried with a nitrogen stream. The substrates were treated with UV/ozone for 30 min to remove the last traces of organic residues. The compact TiO2 layer was coated on the FTO glass by spin-coating a mildly acidic titanium isopropoxide solution, followed by heating at 150 \\u00b0C for 15 min, and then the compact TiO2 films were gradually heated to 500 \\u00b0C and baked at this temperature for 30 min. After cooling to room temperature, mesoporous TiO2 (m-TiO2) layer was deposited on compact-TiO2/FTO substrates via spin coating of 18NR-T diluted in ethanol. The layers were then dried at 125 \\u00b0C for 10 min and sintered at 500 \\u00b0C for 30 min. The perovskite precursor solution was spin coated onto the TiO2/FTO substrates at 3000 rpm for 55 s. During the spin-coating, 100 \\u03bcL of chlorobenzene was dropped in the center of the substrates (2 cm \\u00d7 2 cm) after six seconds. The spin-coated films were heated at 100 \\u00b0C for 20 min, resulting in the formation of dark brown perovskite films. Subsequently, HTMs were deposited on the CH3NH3PbI3 layers by spin coating. Finally, Au electrode was thermally evaporated on the HTM-coated film and the active area of each device was 0.09 cm2.\\n\\nThe thermal stability analysis (TGA) of HTMs was recorded by TA Instruments TGA-Q50 under nitrogen flowing and heating at rate of 10 \\u00b0C min\\u22121. The UV\\u2013vis absorption spectra in dichloromethane solution were measured by HITACHI (model U-2910) UV\\u2013vis spectrophotometer. Emission spectra were performed using a HITACHI (model F-4600) spectrophotometer. Cyclic voltammetry (CV) experiments were performed in dichloromethane with a three electrode configuration consisting of a Pt wire counter electrode, a Ag/AgCl (saturated KCl) reference electrode and a Pt disk working electrode, using 0.1 M n-Bu4NPF6 as the supporting electrolyte. The surface morphology of the perovskite film was observed by scanning electron microscope (SEM, JEOL JSM-7600F). The J-V curves of the PSCs were measured using an electrochemical workstation (CHI 660E, Shanghai Chenhua) under AM 1.5G simulated solar light (100 mW cm\\u22122) (CHF-XM-500W, Trusttech Co. Ltd., Beijing, China). The incident light intensity was calibrated with a standard Si solar cell. The spectra of monochromatic incident photon-to-current conversion efficiency (IPCE) for solar cells were performed by using a commercial setup (QTest Station 2000 IPCE Measurement System, CROWNTECH, USA).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: LHTM-1,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All used reagents were analytical grade (AR.) and purchased from Sigma-Aldrich Corp, unless specifically mentioned. Spiro-OMeTAD was supplied by Luminescence Technology Corp, Taiwan, China. Formamidinium iodide (FAI) and methylammonium bromide (MABr) salts were supplied by Xi'an Polymer Light Technology Corp, China. TiO2 and NiO NCs were synthesized as previously reported (The detailed procedures for the synthesis of TiO2 and NiO NCs can be found in the supporting information and the basic characteristics of NiO NCs are shown in Fig.\\u00a0S1) [,]. FTOs with sheet resistance of 15\\u202f\\u03a9 sq\\u22121 were purchased from Nippon Glass Co. JP.\\n\\nThe 1.2\\u202fM Cs0.05(MA0.15FA0.85)0.95Pb(I0.85Br0.15)3 PVK precursor was prepared in a mixed solvent of anhydrous N, N-dimethylformamide (DMF) and dimethyl sulphoxide (DMSO) with a volume ratio of 4:1 []. The molar ratios of PbI2/PbBr2, FAI/MABr, CsI/(FAI\\u00a0+\\u00a0MABr) and (FAI\\u00a0+\\u00a0MaBr\\u00a0+\\u00a0CsI)/(PbI2+PbBr2) were fixed at 0.85:0.15, 0.05:0.95 and 1:1, respectively.\\n\\nThe FTOs were firstly cleaned by UV-ozone treatment for 15\\u202fmin, followed by consecutive cleaning with detergent and ethanol. The BF4 \\u2212-capped TiO2 NCs dispersed in DMF (20\\u202fmg\\u202fmL\\u22121) was used for preparing TiO2 ETLs on the cleared FTOs by spin-coating the dispersion at 4000\\u202frpm for 30\\u202fs following with a low-temperature thermal treatment at 150\\u202f\\u00b0C for 30\\u202fmin []. The PVK films were prepared on the TiO2 ETLs with the Cs0.05(MA0.15FA0.85)0.95Pb(I0.85Br0.15)3 PVK precursor solution, which was spin-coated at 1000\\u202frpm for 10\\u202fs following with 6500\\u202frpm for 20\\u202fs. Chlorobenzene was used as anti-solvent to extract residual DMF and DMSO in the PVK films. Soon afterwards, the PVK films were heated at 100\\u202f\\u00b0C for 30\\u202fmin.\\nThe oleylamine (OAm) capped NiO NCs dispersed in toluene with different concentrations were spin-coated on the PVK films at 700\\u202frpm for 5\\u202fs and 2000\\u202frpm for 5\\u202fs following with thermal treatment at 70\\u202f\\u00b0C for 10\\u202fmin to form NiO thin films in the interfaces between the PVK and the spiro-OMeTAD HTL of the planar PSCs. The spiro-OMeTAD solution containing 72.3\\u202fmg spiro-OMeTAD, 28.8\\u202f\\u03bcL 4-tert-butyl pyridine, 17.5\\u202f\\u03bcL lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520\\u202fmg Li-TSFI dissolved in 1\\u202fmL acetonitrile) and 1\\u202fmL chlorobenzene was prepared firstly, and then 20\\u202f\\u03bcL of the spiro-OMeTAD stock solution was spin-coated on the NiO thin films at 4000\\u202frpm for 30\\u202fs. Finally, 100\\u202fnm Au electrodes were thermally evaporated on the spiro-OMeTAD HTLs under high vacuum through a shadow mask.\\n\\nThe top and cross-sectional morphologies of PVK films were characterized by a scanning electron microscopy (SEM, Hitachi S-4800). The surface roughness was characterized by an atomic force microscopy (AFM, Bruker Multimode 8). The element analyzation was characterized by an energy dispersion spectrum (EDS, Oxford Inca). The UV\\u2013Vis absorption spectra were analyzed using an UV\\u2013Vis\\u2013NIR spectrometer (Lambda 950). The steady-state photoluminescence (PL) spectra were acquired using a fluorescence spectrophotometer (Thermo Scientific Lumina). The time-resolved photoluminescence (TRPL) spectra were obtained using the time-correlated single-photon counting technique (Omni-\\u03bb Monochromator), and the excitation light pulse was provided using a picosecond diode laser at a 756\\u202fnm wavelength.\\nThe current density-voltage (J-V) characteristic curves of the PSCs were recorded with a computer-controlled Keithley 2400 source meter under simulated AM 1.5\\u202fG solar illumination at 100\\u202fmW\\u202fcm\\u22122 from #94043A solar simulator (PVIV-94043A, Newport, USA) in an air environment. The voltage step and delay time were 20\\u202fmV and 10\\u202fms, respectively. The forward scan started from\\u00a0\\u22120.1\\u202fV to 1.2\\u202fV, while reverse scan from 1.2\\u202fV to\\u00a0\\u22120.1\\u202fV. The steady-state current density (Jsc) and power output were recorded close to the maximum power point, which was extracted from the J-V curves. The incident-photo-to-current conversion efficiency (IPCE) curves were measured as a function of wavelength from 300 to 850\\u202fnm using the Newport IPCE system (Newport, USA). The PSCs with the active area of 0.12\\u202fcm2 (calibrated with a black metal mask with the area of 0.3\\u202f\\u00d7\\u202f0.4\\u202fcm2) and without any encapsulation were prepared for measurements. One batch of 30 devices for each changed condition was prepared and measured. The electrochemical impedance spectroscopy (EIS) measurements were conducted on a Zennium electrochemical workstation (IM6) in dark conditions with the frequencies from 100\\u202fmHz to 2\\u202fM\\u202fHz, the bias of 0\\u202fV and the amplitude of 20\\u202fmV. The capacitance-frequency curves of the devices were obtained with EIS measurement by varying AC frequency at short circuit condition and the capacitance-voltage curves by fixing the AC frequency at 1\\u202fkHZ and varying the bias voltage.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-np,\\n ETL_additives_compounds: BF4,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.45I2.55,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: NiO-np | Spiro-MeOTAD,\\n HTL_additives_compounds: Oleylamine | Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"TiO2NPs were synthesized through a hydrothermal process as we reported earlier [,]. Briefly, a solution containing 0.014\\u202fmol of acetic acid and 0.014\\u202fmol of titanium tetraisopropoxide (TTIP) was prepared and stirred for about 15\\u202fmin. Then 19.6\\u202fml of DI water was added to this solution and vigorously stirred for the hydrolysis process. Afterward, a quantity of 0.26\\u202fml HNO3was injected and solution was refluxed at 80\\u202f\\u00b0C for 75\\u202fmin. This stage was carried out for the peptization and preparation of a pale blue TiO2sol. The solution was normally cooled down to the room temperature and placed into a teflon-lined stainless steel autoclave. Then it was heated at 230\\u202f\\u00b0C for 12\\u202fh to prepare a white precipitate of TiO2NCs.\\n\\nTiO2NRs were also prepared by another hydrothermal process. For this purpose, 6.0\\u202fg of the commercially available P25 TiO2powder was mixed with 33.0\\u202fml of NaOH solution with 15\\u202fM concentration. Then it was stirred at room temperature for 15\\u202fmin and transferred to a teflon-lined autoclave and heated at 170\\u202f\\u00b0C for 72\\u202fh. The obtained precipitate was centrifuged and washed with distilled water and ethanol and soaked in 0.1\\u202fM HCl solution for 24\\u202fh. The final precipitate was repeatedly centrifuged and washed with distilled water to result in an aqueous solution with pH value of 7.0. Finally, the nanorods powder was annealed at 700\\u202f\\u00b0C for 2\\u202fh for better crystalline quality.\\n\\nThe white precipitate of TiO2NCs in water was sonicated with an ultrasonic horn (240\\u00a0W, 120*0.5) in the first stage []. Then it was heated at 40\\u202f\\u00b0C and concentrated to form a 13\\u202fwt% sol of TiO2NCs in water. The solution was centrifuged and washed with ethanol for several times to achieve a 40\\u00a0wt% white precipitate of NCs in ethanol. The total precipitate (about 1.9\\u00a0g) was quite dispersed in proper amount of ethanol in ultrasonic bath for 20\\u00a0min. In parallel, two other solutions containing terpineol in ethanol and ethyl cellulose in ethanol (5\\u201315\\u00a0mPa; 56% and 15\\u201330\\u00a0mPa; 44%) were prepared and slowly added to the NCs solution. The final mixture was sonicated with an ultrasonic horn (240\\u00a0W, 120*0.5\\u00a0s) for three times for well-dispersion. Finally, the ethanol solvent was vacuum evaporated to form a TiO2paste composed of 20\\u202fwt%, 71\\u202fwt% and 9\\u202fwt% of TiO2NCs, terpineol and ethyl cellulose respectively.\\nFor preparation of TiO2NCs/NRs combinative paste, the as-prepared TiO2NRs powder was dispersed in ethanol solution with a weight ratio of 1:5.5. In parallel, the fabricated 20\\u202fwt% TiO2NCs paste was diluted by ethanol with similar 1:5.5\\u202fwt ratio. Then the specific amounts of diluted solutions (with calculated values of TiO2NCs and NRs) were mixed to form diluted combinative pastes with TiO2NRs/(TiO2NCs\\u00a0+\\u00a0TiO2NRs) weight ratios in the range of 0\\u201320%. These solutions were finally heated at 40\\u202f\\u00b0C for preparation of 20\\u202fwt% combinative TiO2NCs/NRs pastes.\\n\\nFluorine-doped tin oxide (FTO) substrates were etched with Zinc powder and diluted HCl for electrical isolation of the photoanode and cathode electrodes. Then, they were cleaned by sonication in ethanol, acetone, DI water and isopropanol for successive 15\\u202fmin, respectively. Afterward, the substrates were heated at 450\\u202f\\u00b0C for 15\\u202fmin and subjected to a UV-Ozone treatment to remove the traces of organic residues. A compact TiO2layer was subsequently spin-coated at 2000\\u202frpm, for 30\\u202fs on the pre-treated substrates. A 0.15\\u202fM solution of TTIP in anhydrous ethanol was normally applied in this deposition stage. Then a heating process was carried out at 500\\u202f\\u00b0C for 1\\u202fh to prepare a severely attached TiO2compact layer on the TCO surfaces. The as-prepared combinative pastes of TiO2NPs and NRs were diluted in ethanol solutions (1:5.5\\u202fwt ratio). Then they were deposited on FTO/compact TiO2layers by spin-coating method performed at 4000\\u202frpm for 30\\u202fs. These layers were finally annealed at 500\\u202f\\u00b0C for 30\\u202fmin to remove the including terpineol and ethyl cellulose and form the appropriate anatase phase of the TiO2.\\nFor the deposition of the Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3perovskite layer a solution containing FAI (1\\u202fM), CsI (0.05\\u202fM), PbI2(1.1\\u202fM), MABr (0.2\\u202fM), and PbBr2(0.22\\u202fM) in anhydrous DMF: DMSO solvent (4:1\\u202fvol ratio) was prepared in the first stage. Then it was coated on FTO/compact TiO2/Mesoporous TiO2NCs-NRs substrates by spin coating approach through a two-step procedure at 1000\\u202frpm, 10s and 4000\\u202frpm for 20s. The anti-solvent chlorobenzene solution was slowly poured at final 6\\u202fs of the second step of spin coating process. The as-prepared multi-layers were subsequently heated at 100\\u202f\\u00b0C for 1\\u202fh.\\nThe Spiro-OMeTAD hole transport layer was over-deposited by another spin-coating process at 5000\\u202frpm for 30\\u202fs. In this stage a solution containing 72.3\\u202fmg of Spiro-OMeTAD in 1\\u202fml of chlorobenzene, 17.5\\u202f\\u03bcl of a 520\\u202fmg\\u202fml\\u22121solution of lithium bis(trifluoromethylsulfonyl)imide (Li-TFSI) in acetonitrile and 28.8\\u202f\\u202f\\u03bcl of 4-tert-butylpyridine (TBP,Sigma-Aldrich) was utilized. Finally, the Au metallic contact was deposited by a thermal evaporation technique.\\n\\nThe X-ray diffraction patterns were measured using PANalytical, X\\u2019Pert Pro MPD equipment with Cu K\\u03b1(\\u03bb\\u202f=\\u202f1.54\\u202f\\u00c5) radiation. UV\\u2013Vis absorption spectra were taken by a Perkin Elmer Lambda 25 spectrophotometer. SEM images were recorded using a TESCAN\\u2013Mira3 field-emission scanning electron microscope. Incident photon-to-current conversion efficiency measurements (IPCE) were carried out by a Sharif solar IPCE-015 equipment. The photocurrent-voltage analyses were performed under AM 1.5 (100\\u202fmW/cm2) simulated light radiation by a Sharif solar SIM-1000 system (calibrated by a Thorlabs photodiode). These measurements were done by masking the active area of the cells with a mask with an open area of 0.09\\u202fcm2. The J\\u2013V curves were recorded by a Keithley 2400 source meter in reverse scan state from 1.1\\u202fV to\\u00a0\\u22120.1\\u202fV and the scan rate of 5\\u202fmV\\u202fs\\u22121. The steady state photoluminescence (PL) spectra were measured using an Avaspec 2048TECspectrophotometer. In this stage the samples were excited by a LCM-DTL-374QT laser equipment with a wavelength of 350\\u202fnm. Then the emitted light of samples was transferred to the spectrophotometer through the optical fibers. The electrochemical impedance spectroscopies (EIS) were finally performed using an Ivium, Compactstat potentiostat/galvanostat in dark and under a reverse bias of\\u00a0\\u22120.9\\u202fV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The patterned ITO glass (\\u223c10\\u202f\\u03a9/square) was purchased from China Southern Glass Holding Corp. CsI (99.5%), FAI (99.5%), MAI (99.5%), PbI2 (99.99%), PbBr2 (99.99%), MABr (99.5%), 2,2\\u2032,7,7\\u2032-tetrakis(N,N\\u2019-di-p-methoxyphenylamine)-9,9\\u2032- spirobifuorene) (Spiro-OMeTAD) (99.8%) was purchased from Xi\\u2019an Polymer Light Technology Corp. without further purification. SnCl2.2H2O (99.995%), chlorobenzene (99.9%), DMF (99%), Lithium bis(trifluoromethanesulfonyl) imide (Li-TFSI) (99.95%) was purchased from Sigma-Aldrich. DMSO (99%) was purchased from Alfa Aesar. Acetonitrile (99.9%) was purchased from Acros, 4-tert-butylpyridine (96%) was purchased from TCI.\\n\\n1\\u202fmmol CH4N2S was added into 20\\u202fml NaOH solution (0.1\\u202fmol) with stirring until it became a homogeneous solution. Then 0.1\\u202fmmol Bi2O3 powder was added into the solution with vigorous stirring, the color of the solution turn into white. Subsequently, the white mixture solution was transferred into a polytetrafluoroethylene (PTFE) lined pressure autoclave with a thermal annealing at 180\\u00b0 for 40\\u202fh. The products were treated by centrifugation and washing with water and anhydrous ethanol step by step. Bi2O2S powder was obtained after all the above process, which is proved to be pure phase by powder X-ray diffraction (XRD). Finally, prepared Bi2O2S powder was dispersed into ethanol with vigorously ultrasonic concussion. The stock solution was ready for use after filtered with 0.45\\u202f\\u03bcm PTFE filter.\\n\\nTo prepare ETL precursor solution with sol-gel method, 90\\u202fmg SnCl2\\u00b72H2O was dissolved in 4\\u202fmL anhydrous ethyl alcohol with stirring and aged for 48\\u202fh to form 22.5\\u202fmg/mL SnCl2\\u00b72H2O solution stock. Then Bi2O2S ethanol solution (0%, 2%, 5%, 10% volume concentration) were added into SnCl2\\u00b72H2O stock to form ETL precursor solution.\\nTo prepare MAPbI3 perovskite precursor solution, 580.9\\u202fmg PbI2 was mixed with 190.8\\u202fmg CH3NH3I at 1.05:1\\u202fM ratio in 900\\u202f\\u03bcL anhydrous DMF and 100\\u202f\\u03bcL anhydrous DMSO solution.\\nTo prepare (CsFAMA)Pb(IBr)3 mixed perovskite precursor solution, 1\\u202fmol FAI, 1.1\\u202fmol PbI2, 0.2\\u202fmol MABr, 0.2\\u202fmol PbBr2 was dissolved in a mixture solvent of DMF/DMSO (4:1, by volume). Next, 50\\u202f\\u03bcL CsI solution (pre-dissolved as a 1.5\\u202fmol stock solution in DMSO) was added to the mixed solution to achieve the desired perovskite precursor solution with proper excess lead halide.\\nTo prepare HTL solution, 72\\u202fmg Spiro-OMeTAD was dissolved into 1\\u202fmL chlorobenzene, with addition of 29\\u202f\\u03bcL of 4-tert-butylpyridine and 18\\u202f\\u03bcL of Li-TFSI solution. Li-TFSI solution was prepared by dissolving 520\\u202fmg Li-TFSI into 1\\u202fml acetonitrile in advance.\\n\\nITO-coated substrates were cleaned by sonication with detergent, deionized water, acetone and isopropanol sequentially for 15\\u202fmin. After blowing with N2, ITO was treated with oxygen plasma for 10\\u202fmin. 35\\u202f\\u03bcL ETL precursor solution was cast onto as treated ITO at 4000\\u202frpm for 30\\u202fs. Subsequently, the substrate was placed on a hot plate at 190\\u202f\\u00b0C for 1\\u202fh (thin film with Bi2O2S modification was named Bi2O2S:SnO2). The as deposited ETLs were then treated with oxygen plasma for 10\\u202fmin. Perovskite precursor solution was spin-coated onto ETL sequentially at 1000\\u202frpm for 5\\u202fs, 3500\\u202frpm for 40\\u202fs, followed by quickly drop-casting 200\\u202f\\u03bcL chlorobenzene as anti-solvent within 10\\u202fs. The sample was quickly transferred to 100\\u202f\\u00b0C hot substrate for 15\\u202fmin. The as prepared Spiro-OMeTAD solution was spin-coated onto the perovskite layer at 4000\\u202frpm for 30\\u202fs. The sample was put into a desiccator overnight to ensure adequate oxidation of HTL. Then 2\\u202fnm molybdenum trioxide (MoO3) was evaporated onto HTL with a module defining active area 0.15\\u202fcm2\\u202fat a vacuum of 2.8\\u202f\\u00d7\\u202f10\\u22124\\u202fPa, followed by the final Ag cathode deposition (80\\u202fnm).\\n\\nThe UV\\u2013vis spectra of ETL were measured with a HP 8453 spectrophotometer. Absorbance spectra of the perovskite films were recorded with a PerkinElmer Lambda 750 UV/VIS/NIR spectrophotometer. Photoluminescence spectra (PL) were measured on a SPEX 1681 automated spectrofluorometer. The Raman spectra were recorded on an inVia-58P056 Raman spectrometer, using 532\\u202fnm focused excitation laser. Scanning electron microscopy (SEM) that visualizes film morphology was carried out on ZEISS Merlin. Structural analysis of the thin films was carried out via high-resolution XRD Bruker Discovery 08 with a Hi-Star area detector. The chemical analysis of SnO2 and SnO2:Bi2O2S was recorded on Kratos Axis Ulra DLD X-ray photoelectron spectroscopy (XPS) under conditions of Al K\\u03b1 monochromatic X-ray source. Curve fitting and background subtraction of XPS data was processed using CASA XPS software. The work function (WF) of SnO2 and SnO2:Bi2O2S thin film was measured with Kelvin Probe using KP Technology SKP5050. The current density-voltage (J-V) characteristics of PVSCs were recorded using a computer controlled Keithley 2400 source unit under a calibrated AM 1.5\\u202fG solar simulator (100\\u202fmW\\u202fcm\\u22122) at room temperature.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Bi2O2S-np,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 110,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I was synthesized according to the reported procedure: a hydroiodic acid (30 mL, 0.227 mol, 57 wt% in water, Aldrich) and a slightly excess methylamine (32 mL, 0.273 mol, 40% in methanol, Aldrich) were stirred in the ice bath for 2 h. The resulting solution was concentrated with rotary evaporation for 1 h at 50 \\u00b0C to evaporate the solvent. The precipitate was washed with diethyl ether for three times, and dried under vacuum for 24 h, and used without further purification. PbI2 (5 g) was dissolved in dimethylsulfoxide (DMSO, 15 mL) at 60 \\u00b0C, and then toluene (35 mL) was slowly added into the PbI2 solution. Then, the white PbI2(DMSO)2 precipitate was filtered and dried for 3 h at room temperature. The PbI2(DMSO)2 was then put in vacuum oven for 24 h at 60 \\u00b0C, losing one molecule of DMSO. Finally, the PbI2(DMSO) complex was obtained.\\n\\n2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9\\u2032-spirobifluorene (spiro-OMeTAD, Merck, 0.723 g), an additive (17.5 \\u00b5L) of Li-bis (trifluoromethanesulfonyl) imide (LiTFSI)/acetonitrile (LiTFSI, 99.95%, Aldrich, 520 mg/1 mL), and 4-tert-butylpyridine (TBP, 96%, Aldrich, 29 \\u00b5L) were added in chlorobenzene (99.8%, Aldrich, 1 mL).\\n\\nThe PSCs was fabricated in the air. F-doped SnO2-layered glass (FTO) was patterned with Zn power and HCl aqueous solution. Titanium diisopropoxide bis(acetylacetonate) solution in isopropanol was spin-coated at the patterned glass (3000 rpm, 30 s), followed by sintering for 60 min at 450 \\u00b0C in the furnace. The dense blocking layer of TiO2 was formed to prevent direct contact between FTO and the hole-conducting layer. A mesoporous TiO2 film with the thickness of 200\\u2013300 nm was spin-coated on the bl-TiO2/FTO substrate (5000 rpm, 30 s, TiO2 paste was diluted in ethanol at TiO2:EtOH=1:5.5, weight fraction), followed by sintering for 60 min at 500 \\u00b0C in the furnace to remove the organic components. Perovskite layer was formed on these mesoporous layers. PbI2(DMSO) complex solution (1.30 M) in N,N-Dimethylformamide (DMF) was prepared at 70 \\u00b0C. The PbI2(DMSO) complex solution was spin-coated on mp-TiO2 substrate at 3000 rpm for 30 s. Then, MAI solution (465 mM) in 2-propanol was dropped on the top of the transparent PbI2(DMSO), after one minutes' standing, spin-coating at 5000 rpm for 30 s. The films changed to dark brown in colour during spin-coating, and the films were dried on a hot plate for 20 min at 150 \\u00b0C. Then, the CH3NH3PbI3-sensitized TiO2 films were coated with HTM solution using spin-coating method at 3000 rpm for 30 s. The counter electrode was deposited using the magnetron sputtering technique (Denton Vacuum). The metallic contact thin films were deposited using DC reactive magnetron sputtering method. The sputtering source was 3 mm thick water-cooled solid (Ag, Cu, Ni, W, and Mo) target (nominal purity of 99.999%) with 75.4 mm in diameter. The distance between target and substrate was adjusted to 7 cm. The sputtering chamber was evacuated to a base pressure of 5\\u00d710\\u22126 Torr. Then, Ar was let into the chamber through volume flow meters with the flow rate of 20 sccm. In order to remove the surface oxide layer on the target, a pre-sputtering process was carried out for 5 min in Ar atmosphere. The total pressure, sputtering voltage and current for deposition were fixed as 0.3 Pa, 0.39 kV and 0.4 A, respectively. The Ag target was ignited at the power of 1 W, and sputtered for 70 min. The Cu target was ignited at the power of 10 W, and sputtered for 25 min. The Ni, W, and Mo targets were ignited at the power of 80 W, and sputtered for 30 min.\\n\\nX-ray diffraction patterns were collected using a XRD diffractometer (Rigaku, MiniFlex II) with Cu K\\u03b1 radiation at scan rate of 3\\u00b0 min\\u22121. SEM instrument (SUPRA 55VP) was used to acquire surface/cross-section images with an electron beam accelerated at 15 kV. Transmission electron microscopy (TEM, JEM-2010FEF, JEOL) was used to probe the microstructure of MAPbI3 grains in the mp-TiO2/MAPbI3 layer and MAPbI3 capping layer.\\nThe J\\u2013V curves were measured with electrochemical workstation (Zahner IM6ex) using a solar simulator at 100 mW cm\\u22122 illumination (AM 1.5 G) and a calibrated Si-reference cell certificated by NREL. The J\\u2013V curves were measured by reverse and forward scans. The step voltage and the delay time were fixed at 10 mV and 40 ms, respectively. The J\\u2013V curves for all devices were measured by masking the active area with a metal mask (area of 0.1 cm2). The electrochemical impedance spectra (EIS) was measured under a solar simulator at 100 mW cm\\u22122 illumination (AM 1.5 G) at 0-bias in electrochemical workstation (Zahner IM6ex). The impedance spectra were simulated using the ZView software (Scribner Associates Inc.).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 150.0,\\n Perovskite_deposition_thermal_annealing_time: 1.0 >> 20.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Sputtering,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"None of the materials and chemicals used were further treated. SnO2 colloid precursor was purchased from Alfa Aesar (15% in H2O colloidal dispersion). N, N-dimethylformamide (DMF, 99.8%, anhydrous), dimethylsulfoxide (DMSO, 99.9%, anhydrous), acetonitrile (ACN, 99.8%, anhydrous), and chlorobenzene (CB, 99.8%, anhydrous) were purchased from Sigma-Aldrich. SpiroOMeTAD (99.8%) was purchased from Lumtech. Bis(trifluoromethane) sulfonamide lithium salt (LiTFSI, >99%) was from Sigma-Aldrich. 4-tert-butylpyridine (tBP, >96%), lead (II) iodide (PbI2, 99.99%), lead bromide (PbBr2, 99.99%), cesium iodide (CsI, 99.99%), and formamidinium iodide (FAI, \\u226599.5%) were bought from Xi\\u2019an Polymer Light Technology Corp.\\n\\nThe device was fabricated with an architecture of tin-doped indium oxide (ITO) -coated glass/SnO2/Cs0.2FA0.8Pb(I0.7Br0.3)3/spiroOMeTAD/Ag. The ITO substrate was cleaned by detergent, acetone, isopropanol, and ethanol for each 15\\u00a0min, respectively. For better wetting of the SnO2 precursor solution, the cleaned ITO was treated with ozone-ultraviolet for 15\\u00a0min. The SnO2 precursor solution (diluted by deionized water into 2.67% concentration) was spin-coated onto the ITO substrate at 4000 r.p.m. for 20\\u00a0s, and annealed in ambient air at 180\\u2103 for 20\\u00a0min. Afterward, ozone-ultraviolet treatment was adopted for 15\\u00a0min to enhance the wettability of the perovskite precursor on the SnO2 surface. The perovskite precursor solution was prepared by dissolving 0.2\\u00a0mmol CsI, 0.8\\u00a0mmol FAI, 0.55\\u00a0mmol PbI2 and 0.45\\u00a0mmol PbBr2 in 1\\u00a0mL mixture of DMF/DMSO (3:1\\u00a0vol ratio). For the KBF4 containing samples, 1\\u00a0mg KBF4 was directly added into the precursor solution. The precursor solution was then coated onto the ITO/SnO2 substrates by two consecutive spin-coating steps at 1,000 r.p.m. and 5,000 r.p.m. for 10\\u00a0s and 30\\u00a0s, respectively. 100\\u00a0\\u00b5L chlorobenzene was dropped on the spinning substrate before the end of the second process. The samples were annealed on the hot plate at 100\\u00a0\\u00b0C for 30\\u00a0min to obtain a uniform film. After cooling to room temperature, the spiroOMeTAD layer was formed by spin-coating at 4000 r.p.m. for 30\\u00a0s. The spiroOMeTAD precursor solution was prepared by dissolving 72.3\\u00a0mg of spiroOMeTAD, 17.5\\u00a0\\u03bcL of LiTFSI stock solution (520\\u00a0mg\\u00b7mL\\u22121 in acetonitrile), and 29\\u00a0\\u03bcL tBP in 1\\u00a0mL chlorobenzene. Finally, 100\\u00a0nm metal electrode of the silver film was deposited by thermal evaporation through shadow masks to define the active area to 0.105\\u00a0cm2.\\n\\nThe top-viewed and cross-sectional scanning electron microscope (SEM) images films were observed using scanning electron microscope (FEI INSPECT F50, U.S.A.) and the energy-dispersive spectroscopy (EDS) was equipped on scanning electron microscope. Atomic force microscope (AFM) images were scanned by atomic force microscope (AFM, KEYSIGHT Technologies 7500). X-ray diffraction (XRD) measurements were performed on X-ray diffractometer (PANalytical B.V., X\\u2019 Pert Pro MPD) with Cu K\\u03b1 radiation (\\u03bb\\u00a0=\\u00a01.54050\\u00a0\\u00c5). X-ray photoelectron spectroscopy (XPS) (Thermo Fisher scientific, Al K\\u03b1 radiation) analysis was employed to demonstrate the chemical bonding at the surface. The ultraviolet absorption spectra (UV\\u2013vis) of the perovskite films were measure from the absorbance model (with integrating sphere) using a UV-3600 spectrophotometer (Shimadzu Corporation) in the range of 300\\u2013800\\u00a0nm at a step bandwidth of 1\\u00a0nm. Steady-state and time-resolved photoluminescence (PL) were characterized by an FLS980 (Edinburgh Instruments Ltd) with an excitation at 468\\u00a0nm. The current-voltage (J-V) characteristics were measured by a Keithley B2901A source and the solar simulator with standard AM 1.5G (100\\u00a0mW\\u00b7cm\\u22122, SS-F5-3A, Enlitech) under ambient conditions. The J-V curves were measured by forward (\\u22120.1\\u00a0V to 1.3\\u00a0V forward bias) or reverse (1.3\\u00a0V to \\u22120.1\\u00a0V) scans with a delay time of 10\\u00a0ms for each point. The external quantum efficiency (EQE) spectrum of the devices was characterized using a Bentham PVE300 Photovoltaic Device Characterization System by illuminating the solar cell with modulated monochromatic light, and the measurement scope was 300\\u2013800\\u00a0nm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: ,\\n ETL_stack_sequence: SnO2,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: ,\\n Perovskite_composition_long_form: Cs0.2FA0.8PbBr0.3I0.7,\\n Perovskite_composition_short_form: CsFAPbBrI,\\n Perovskite_additives_compounds: KBF4,\\n Perovskite_deposition_solvents: ,\\n Perovskite_deposition_procedure: ,\\n Perovskite_deposition_thermal_annealing_temperature: ,\\n Perovskite_deposition_thermal_annealing_time: ,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: ,\\n Backcontact_stack_sequence: ,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: ,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: ,\\n Stability_atmosphere: ,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: ,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: Unknown,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"SnCl2\\u20222H2O, PbI2, isopropanol and anhydrous dimethylformamide (DMF) were used without further purification. 40\\u00a0\\u00b5L PbI2 solution was spin-coated on the compact SnO2 layer at 3000\\u00a0rpm for 30\\u00a0s, which was dried at 75\\u00a0\\u00b0C for 30\\u00a0min. 40\\u00a0\\u00b5L MAI:MACl solution was loaded on the PbI2 substrate with spun at 3000\\u00a0rpm for 30\\u00a0s and then dried at 135\\u00a0\\u00b0C for 5\\u201315\\u00a0min in dry air.\\nTo a mixture of 1 (132.6\\u00a0mg, 0.459\\u00a0mmol), DTPBT (100\\u00a0mg, 0.153\\u00a0mmol) and K2CO3 aqueous solution (2\\u00a0M, 0.46\\u00a0mL) in THF (15\\u00a0mL), Pd(PPh3)4 was added as catalyst. The reaction mixture was stirred for 16\\u00a0h under argon atmosphere at 70\\u00a0\\u00b0C. After cooling to room temperature, 20\\u00a0mL of water was added to the reaction mixture, the mixture was extracted with CH2Cl2 three times and dried over MgSO4. After removal of the solvent under reduced pressure, the residue was purified by column chromatography on silica gel (petroleum ether/ethyl acetate/dichloromethane, v/v/v\\u202f=\\u202f30/1/1) to give HZ1 as a red solid in 73% yield (110\\u00a0mg), mp 248\\u2013250\\u00a0\\u00b0C. 1H NMR (400\\u00a0MHz, CDCl3) \\u03b4 7.57 (d, J\\u00a0=\\u00a08.4\\u00a0Hz, 4H), 7.30\\u20137.27 (m, 10H), 7.16\\u20137.04 (m, 16H), 4.47 (t, J\\u00a0=\\u00a07.4\\u00a0Hz, 4H), 1.89\\u20131.84 (m, 4H), 1.20 (m, 12H), 0.80\\u20130.77 (m, 6H). The 1H NMR peak at about \\u03b4\\u202f=\\u202f1.5\\u00a0ppm is according to the proton of H2O from the deuterium reagents. 13C NMR (100\\u00a0MHz, CDCl3) \\u03b4 147.9, 147.8, 147.8, 146.2, 146.0, 131.8, 129.7, 129.6, 126.7, 125.0, 124.0, 123.6, 120.4, 111.4, 107.0, 50.7, 31.6, 30.4, 26.7, 22.8, 14.2. HRMS (ESI, m/z): [M\\u00a0+\\u00a0Na]+ calcd for C62H56N6NaS3: 1003.3621, found: 1003.3642.\\n\\nThe synthesis procedure for HZ2 was similar to that of HZ1, except compound 2 instead of 1 was used in 68% yield, mp 138\\u2013140\\u00a0\\u00b0C. 1H NMR (400\\u00a0MHz, CDCl3) \\u03b4 7.46\\u20137.41 (m, 4H), 7.20\\u20137.15 (m, 6H), 6.95\\u20136.91 (m, 2H), 6.87\\u20136.82 (m, 4H), 4.45\\u20134.41 (m, 4H), 3.84 (t, J\\u00a0=\\u00a07.0\\u00a0Hz, 4H), 1.84\\u20131.79 (m, 8H), 1.46\\u20131.41 (m, 4H), 1.31\\u20131.17 (m, 28H), 0.90\\u20130.79 (m, 12H). The 1H NMR peak at about \\u03b4\\u202f=\\u202f1.5\\u00a0ppm is according to the proton of H2O from the deuterium reagents. 13C NMR (100\\u00a0MHz, CDCl3) \\u03b4 147.8, 146.0, 145.2, 145.0, 144.9, 131.6, 130.1, 127.8, 127.7, 125.6, 124.8, 124.4, 124.4, 122.8, 120.3, 115.8, 115.7, 111.2, 106.9, 50.6, 47.9, 32.1, 31.7, 30.5, 29.6, 27.3, 27.2, 26.7, 23.0, 22.8, 14.4, 14.2. HRMS (ESI, m/z): [M\\u00a0+\\u00a0Na]+ calcd for C66H76N6NaS5: 1135.4627, found: 1135.4654.\\n\\nThe synthesis procedure for HZ3 was similar to that of HZ1, except compound 3 instead of 1 was used in 75% yield, mp 186\\u2013188\\u00a0\\u00b0C. 1H NMR (400\\u00a0MHz, CDCl3) \\u03b4 7.50 (d, J\\u00a0=\\u00a08.4\\u00a0Hz, 4H), 7.20 (s, 2H), 7.09 (d, J\\u00a0=\\u00a08.6\\u00a0Hz, 8H), 6.96 (d, J\\u00a0=\\u00a08.4\\u00a0Hz, 4H), 6.86 (d, J\\u00a0=\\u00a08.6\\u00a0Hz, 8H), 4.45\\u20134.42 (m, 4H), 3.96 (t, J\\u00a0=\\u00a06.4\\u00a0Hz, 8H), 1.85\\u20131.77 (m 12H), 1.50\\u20131.47 (m, 8H), 1.38\\u20131.37 (m, 16H), 1.22 (m, 12H), 0.95\\u20130.92 (m, 12H), 0.82\\u20130.80 (m, 6H). 13C NMR (100\\u00a0MHz, CDCl3) \\u03b4 156.0, 148.7, 147.8, 146.3, 146.1, 140.7, 131.5, 127.5, 127.1, 126.4, 120.7, 119.9, 115.7, 111.2, 106.3, 68.6, 50.6, 31.9, 31.6, 30.4, 29.7, 26.7, 26.1, 22.9, 22.8, 14.4, 14.2. HRMS (ESI, m/z): [M\\u00a0+\\u00a0Na]+ calcd for C86H104N6NaO4S3: 1403.7173, found: 1403.7238.\\n\\n\\nThe patterned ITO coated glass was ultrasonically cleaned with detergent water, deionized water, acetone and ethanol for 20\\u00a0min, respectively. The substrate was treated with UV\\u2013O3 for 25\\u00a0min. In brief, a 50\\u00a0nm-thick compact SnO2 layer was deposited onto ITO substrate for 30\\u00a0s at 4000\\u00a0rpm with a ramp of 4000\\u00a0rpm\\u00a0s\\u22121, followed by 150\\u00a0\\u00b0C annealing 30\\u00a0min and 180\\u00a0\\u00b0C annealing 60\\u00a0min in the air. After cooling to room temperature, MAPbI3 \\u2212 xClx film (PbI2\\u00a0=\\u00a0470\\u00a0mg dissolved in 1\\u00a0mL N,N-dimethylforMaMide (DMF), MAI:MACl\\u202f=\\u202f50:5\\u00a0mg dissolved in 1\\u00a0mL isopropanol) was prepared via a modified two-step solution process. After cooling to room temperature, a HTL was coated on the perovskite film at 3000\\u00a0rpm with a ramp of 3000\\u00a0rpm\\u00a0s\\u22121 for 30\\u00a0s. The hole transporting material solution contains 72.3\\u00a0mg spiro-OMeTAD, 28.8\\u00a0\\u00b5L TBP, 17.5\\u00a0\\u00b5L Li-TFSI/acetonitrile (520\\u00a0mg\\u00a0mL\\u22121) per 1\\u00a0mL chlorobenzene, and 30\\u00a0mg HTM (HZ1, HZ2, and HZ3), 334\\u00a0mol% TBP, 54\\u00a0mol% Li-TFSI/acetonitrile (520\\u00a0mg\\u00a0mL\\u22121) per 1\\u00a0mL chlorobenzene. Finally, 80\\u00a0nm gold counter electrode was deposited by thermal evaporation.\\nHole mobility of HTMs (HZ1, HZ2, and HZ3) were measured by using the space-charge-limited current (SCLC) method with the device structure of ITO/MoO3/HTMs/MoO3/Ag. For the hole-only devices, SCLC is described as J=98\\u03b50\\u03b5r\\u03bcV2d3 where J is the current density, \\u00b5 is the zero-field mobility, \\u03b5 0 is the permittivity of the vacuum, \\u03b5 r is the relative permittivity of HTMs, d is the thickness of the HTMs (80\\u00a0nm) and V is the applied effective voltage, respectively.\\nThe crystalline morphology for perovskite films was characterized with a field-emission scanning electron microscopy (FE-SEM). A xenon light source solar simulator (450\\u00a0W, Oriel, model 9119) with an AM 1.5\\u00a0G filter (Oriel, model 91192) was used to give an irradiance of 100\\u00a0mW\\u00a0cm\\u22122 at the surface of the solar cells. The photocurrent\\u2013voltage (J\\u2013V) characteristics of the PSCs were measured by recording the current through Keithley 2400 digital source meter. The devices were tested using a metal mask with an area of 0.108\\u00a0cm2. A similar data-acquisition system was used to control the incident photon conversion efficiency (IPCE) measurements. A white-light bias was applied onto the sample during the IPCE measurements with the direct current (DC) model (130\\u00a0Hz).\\nTime-resolved luminescence decays were recorded with time-correlated single photo counting system (PicoHarp 300, PicoQuant GmbH). The excitation light source was Ti: Sapphire laser (Mira 900, Coherent; 76\\u00a0MHz, 130\\u00a0fs). The photoluminescence (PL) was performed using the VERTEX 70 under the 532\\u00a0nm laser at room temperature.\\nThe contact angles were measured with an optical CA meter (OCA20, Dataphysics) at room temperature.\\n1H and 13C NMR spectra were recorded on a Bruker 400\\u00a0MHz instrument with the solvent CDCl3. The melting point was measured on a SGW X-4B microscopic melting point apparatus. The absorption and emission spectra of the three compounds in CH2Cl2 solution were recorded on a Shimadzu UV-2450 spectrophotometer and a Shimadzu RF-5301\\u00a0PC photoluminescence spectrometer, respectively.\\nThe cyclic volammetry experiments were carried out on an electrochemistry workstation (e-corder (ED 401) poteneiostat) using hole-transporting material (HTM) dichloromethane solutions (1\\u00a0\\u00d7\\u00a010\\u22124\\u00a0M) containing TBAPF6 (0.1\\u00a0M) as a supporting electrolyte at a 50\\u00a0mV/s scan rate. A glass carbon electrode was used as the working electrode, a platinum wire as the counter electrode, Ag/AgCl (3\\u00a0M in KCl) as the reference electrode. The ferrocene/ferrocenium (Fc/Fc+) redox couple was tested as the standard.\\nFor the nanosecond transient absorption spectroscopy, about 50\\u00a0\\u00b5J of pulse energy as the fundamental output from a Ti: Sapphire femtosecond regenerative amplifier (800\\u00a0nm, 35\\u00a0fs FWHM, 1\\u00a0kHz, Newport Spectra-Physics) was used to generate pump and probe beams. By introducing the fundamental beams into an optical parametric amplifier (Light Conversion Ltd.), we could select a certain wavelength from the tunable output as the pump pulses, whereas light continuum probe pulses were obtained by focusing the fundamental beams onto a sapphire plate (contained in LP920, Edinburgh Instruments). The S-4 transmitted probe light from the samples were collected and focused on the broadband VIS-NIR detector for recording the time-resolved excitation induced difference spectrum (\\u0394O.D.).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 75 >> 135,\\n Perovskite_deposition_thermal_annealing_time: 30.0 >> 10.0,\\n HTL_stack_sequence: H-Z1,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.108,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PSCs were fabricated on F-doped SnO2 (NSG10) substrates previously cleaned by a sequential sonication treatment in a 2% Hellmanex solution, acetone, and isopropanol, followed by UV ozone treatment for 15\\u00a0min. These substrates were directly used as described for the ETL-free PSCs. To prepare the other configurations investigated in this article, we deposited a compact blocking layer of TiO2 (c-TiO2, 30\\u00a0nm in thickness) by spray pyrolysis using a titanium diisopropoxide bis(acetylacetonate) solution in ethanol (22% v/v), followed by sintering at 450\\u00b0C for 20\\u00a0min (c-TiO2 electrode). SnO2 electrodes were prepared by spin-coating a precursor solution of SnCl4 (Acros) dissolved in water. For formation of a \\u223c100-nm thick SnO2 layer, 0.5\\u00a0M SnCl4 solution was spin-coated on the UV-ozone-treated FTO substrates at 5,000\\u00a0rpm for\\u00a010 s. The SnO2 film was then transferred onto a hotplate and dried at 100\\u00b0C for 1\\u00a0min, post-annealed at 180\\u00b0C for 1\\u00a0hr, and cooled down before deposition of perovskite. The planar configurations, including the ETL-free cells, were treated by UV ozone for 15\\u00a0min before deposition of the perovskite layer. Finally, a 150-nm thick layer of mesoporous TiO2 (meso-TiO2, 30 NR-D titania paste from Dyesol) was prepared by spin-coating a diluted TiO2 dispersion in ethanol (150\\u00a0mg\\u00b7mL\\u22121) at 2,000\\u00a0rpm for 15\\u00a0s followed by a sintering step at 450\\u00b0C for 30\\u00a0min. Afterward, the meso-TiO2 substrates were lithium-treated by spin-coating 40\\u00a0\\u03bcL of tris(bis(trifluoromethylsulfonyl)imide) (Li-TFSI, 10\\u00a0mg/mL in acetonitrile) onto the mesoporous layer, followed by an additional sintering step at 450\\u00b0C for 20\\u00a0min. After sintering, the c-TiO2/meso-TiO2 electrodes were ready to use and transferred to an N2 controlled atmosphere. The perovskite precursor solution was prepared by mixing CH3NH3I (MAI, Dyesol) and PbI2 (TCI) in N,N\\u2032-dimethylsulfoxide (DMSO) in a molarity of 1.20 for MAPbI3, while for the mixed cation/halide composition formamidinium iodide (FAI), MAI (from Dyesol), PbI2, and PbBr2 (TCI) were mixed in DMF/DMSO (4:1) solvent at 1.25\\u00a0M to form (FAPbI3)0.85(MAPbBr3)0.15, with 5% of PbI2 excess content. The perovskite layers were then fabricated by using a two-step spin-coating process reported by Seok et\\u00a0al. (first step 1,000\\u00a0rpm for 10\\u00a0s; second step 4,000\\u00a0rpm for 30 s), and 10\\u00a0s prior to the end of the program 100\\u00a0\\u03bcL of chlorobenzene was poured onto the films. The substrates were then annealed at 100\\u00b0C for 60\\u00a0min. Afterward, Spiro-OMeTAD was spin-coated at 4,000\\u00a0rpm from a chlorobenzene solution (28.9\\u00a0mg in 400\\u00a0\\u03bcL, 60\\u00a0mmol) containing Li-TFSI (7.0\\u00a0\\u03bcL from a 520\\u00a0mg/mL stock solution in acetonitrile), TBP (11.5\\u00a0\\u03bcL), and Co(II)TFSI (10\\u00a0mol%, 8.8\\u00a0\\u03bcL from a 40\\u00a0mg/mL stock solution) as dopants. Finally, a 70\\u00a0nm gold electrode was evaporated.\\n\\nThe XRD patterns of the prepared films were measured using a D8 Advance diffractometer from Bruker (Bragg-Brentano geometry, with an X-ray tube Cu-K\\u03b1, \\u03bb\\u00a0=\\u00a01.5406\\u00a0\\u00c5). The absorption spectra were registered with a UV-Vis-IR spectrophotometer (PerkinElmer). Photoelectron spectroscopy (PES) measurements were\\u00a0performed in an ultra-high vacuum analysis chamber (base pressure of 2\\u00a0\\u00d7\\u00a010\\u221210\\u00a0mbar) using an He-discharge UV source (Omicron) with an excitation energy of 21.2 eV for UPS. Before the analysis, the samples were treated by UV ozone for 15\\u00a0min in the same conditions as for the device preparation. The photoelectron spectra were recorded using a Phoibos 100 (Specs) hemispherical energy analyzer at a pass energy of 5 eV for the valence band. For work function determination, the secondary electron cutoff (SECO) was recorded by applying a \\u221210\\u00a0V sample bias to clear the analyzer work function. The reported valence band spectra were background subtracted. The binding energies for all the photoemission spectra are referenced to the Fermi level. For the nanosecond-TAS/photoluminescence a nanosecond laser (5\\u00a0ns pulse duration, 10\\u00a0Hz, Ekspla NT342 model) with an integrated optical parametric oscillator system (from 355 to 2,500\\u00a0nm tunability) was used as pump source. This was coupled with the LP980-KS Laser Flash Photolysis Spectrometer used for the measurement of laser-induced transient absorption and the photoluminescence kinetics and spectra. Wavelength-specific kinetic measurements were made using a photomultiplier and a digital storage oscilloscope. The\\u00a0probe light was provided by a pulsed xenon arc lamp. The beams were focused onto the sample on a\\u00a0minimum 5-mm2 diameter area, ensuring the spatial overlap. The transmitted probe was spectrally filtered by a monochromator and detected. From the transmission change following photoexcitation, the variation in the absorption was thus derived as \\u0394O(\\u03c4,\\u03bb)\\u00a0= log(I probe)/(I t(\\u03c4,\\u03bb)), where I probe is the transmitted probe with excitation off and I t is the transmitted probe after laser excitation. The minimum\\u00a0detectable optical density of the LP980-KS using the photomultiplier is \\u0394OD\\u00a0= 0.002 (single-shot, fast-detector option) with a system overall response function of: <7\\u00a0ns (laser limited).\\n\\nThe photovoltaic device performance was analyzed using a VeraSol LED solar simulator (Newport) producing 1 sun AM 1.5 (1,000 W/m2) sunlight. Current-voltage curves were measured in air with a potentiostat (Keithley 2604). The light intensity was calibrated with an NREL-certified KG5 filtered Si reference diode. The solar cells were masked with a metal aperture of 0.16\\u00a0cm2 to define the active area. Current-voltage curves at different scan rates were collected from slowest to fastest scan rate by scanning in the FR direction followed by the RF direction for a given scan rate, with a time interval of 10\\u00a0s (under illumination) before the next measurement. The starting voltage for the FR scan was slightly higher (30\\u00a0mV) than the VOC of the device while for the RF scan, it was 0 V. EQE was measured with the IQE200B (Oriel) without bias light. IS measurements were performed in the dark for a cell area of 0.56\\u00a0cm2. A perturbation amplitude of 10\\u00a0mV was used and the spectra measured over the frequency range 50 mHz to 1 MHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | Li-TFSI,\\n ETL_deposition_procedure: Spray-pyrolys | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PEDOT: PSS (Clevios Al4083, Haraeus), SnI2 (99.99%, Sigma Aldrich), SnF2 (99.5%, Sigma Aldrich), FAI (99%, MaterWin New Material), BCP (99%, Nichem), chlorobenzene (anhydrous 99.8%, Sigma Aldrich), and DMSO (anhydrous 99.8%,\\u00a0Alfa Aesar) were used as received. PPA is synthesized following our previous work. PPAI salt is prepared following the same process of typical MAI salt.\\n\\nTo prepare PPA-modified FASnI3 film, FASnI3 and PPASnI3 precursor solutions were first prepared by dissolving 316.6\\u00a0mg SnI2 (0.85\\u00a0mmol), 146.2\\u00a0mg FAI (0.85\\u00a0mmol), and 13.3\\u00a0mg SnF2 (0.085\\u00a0mmol) respectively, in 1\\u00a0ml DMSO and stirred for 2\\u00a0h under room temperature to form a 0.85\\u00a0M solution. Then different mole ratios of the FASnI3 and PPASnI3 solutions (0%, 5%, 10%, 20%, 40%) were mixed to prepare the PPA, FAI, and SnI2 precursor solutions. To fabricate PPA-modified FASnI3 films, the precursor solution was spin-coated on the substrate at 5,000\\u00a0rpm for 60 s, and 100\\u00a0\\u03bcL chlorobenzene was dropped at the 30th sec after spinning started. Finally, the film was dried at 40\\u00b0C for 2\\u00a0min and 100\\u00b0C for 20\\u00a0min.\\n\\nField emission scanning-electron microscope (SEM) (Quanta250, FEI, USA) and atomic force microscope (AFM, NT-MDT, Russia) were used to investigate the morphology of perovskite film. XRD measurements were performed with an X-ray diffractometer (D/MAX-2400, Rigaku, Japan) with Cu K\\u03b1 radiation. The absorption spectra were acquired on a UV-Vis spectrophotometer (U-3010, Hitachi High-Technologies, Japan). The PL spectra were acquired on a photoluminescence spectroscopy (Fluoromax 4, HORIBA Jobin Yvon, United States). FTIR spectra were measured with a PerkinElmer FT-IR spectrometer. EIS experiments were carried out in under AM 1.5 illumination at 0\\u00a0V with an electrochemical workstation (CHI660C, CH Instruments) in a frequency range from 0.1\\u00a0Hz to 1 mHz. The GIXRD measurements were performed at the BL14B1 beamline of Shanghai Synchrotron Radiation Facility (SSRF) using X-rays with a wavelength of 0.6887\\u00a0\\u00c5, and the incident angle set to 0.3\\u00b0. The 2D-GIXRD patterns were analyzed using Fit 2D software and displayed in scattering-vector q coordinates with q\\u00a0= 4\\u03c0 sin \\u03b8/\\u03bb, where \\u03b8 is half of the diffraction angle, and \\u03bb is the wavelength of the incident X-ray. EIS experiments were carried out in under AM 1.5 illumination at different applied biases with an electrochemical workstation (CHI660C, CH Instruments) in a frequency range from 0.1\\u00a0Hz to 1 mHz. The UPS measurements were carried out by X-ray photoelectron spectroscopy using Au as reference (ESCALAB Xi+, Thermo Fisher Scientific).\\n\\nThe ITO substrate was sequentially cleaned with ultrapure water, acetone, ethanol, and isopropanol. After 10\\u00a0min of UV-O3 treatments, the PEDOT: PSS solution was filtered and spin-coated onto the substrate at 5,000\\u00a0rpm for 60\\u00a0s and then annealed 20\\u00a0min at 170\\u00b0C. After the deposition of the perovskite layer, C60 (30\\u00a0nm) and BCP (8\\u00a0nm) were sequentially evaporated at the rate of 1.0\\u00a0\\u00c5/s. Ag (120\\u00a0nm) was finally evaporated through a shadow mask with an active area of 0.09\\u00a0cm2 or 1\\u00a0cm2 to finish the small-area and large-area devices, respectively. After fabrication, all devices were kept unencapsulated in the glovebox for further measurements.\\n\\nAll measurements were conducted in ambient air. The photovoltaic performance was measured under an AAA solar simulator (XES-301S, SAN-EI), AM 1.5G irradiation with an intensity of 100 mW/cm2 with shadow masks. The photocurrent-voltage (J-V) curve was measured using a Keithley 2602 Source-Meter. Incident photon-to-current conversion efficiency (IPCE) spectra were collected by the solar-cell quantum-efficiency measurement system (SolarCellScan 100, Zolix instruments. Co. Ltd.).\\nFor SCLC measurement, the device structure of ITO/PEDOT: PSS/perovskite/Au was used. The trap-state density in the film can be estimated by the equation: ntrap=2\\u03f50\\u03f5VTFL/qL2 where \\u03f5 is the vacuum permittivity, \\u03f5 0 is the static dielectric constant of FASnI3 (\\u223c5.7), q is the elemental charge, and L is the thickness of the film. The charge mobility in the film can be estimated by the Mott-Gurney equation: \\u03bc=8JL3/9\\u03f50\\u03f5V2 where J/V2 is the slope of J versus V 2 (n\\u00a0= 2) in Child\\u2019s regime (yellow curves) in Figure\\u00a04C.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: FASnI3,\\n Perovskite_composition_short_form: FASnI,\\n Perovskite_additives_compounds: PPAI,\\n Perovskite_deposition_solvents: DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Lead iodide (PbI2, 99.9%) was purchased from Alfa Aesar. Methylammonium iodide (MAI) was purchased from Dyesol. PhNa-1T (electrical conductivity\\u00a0=\\u00a01.3\\u00a0\\u00d7\\u00a010\\u22124\\u00a0S\\u00a0cm\\u22121) was synthesized by following a reported method . All reagents were obtained from Sigma-Aldrich unless specified, and used as received.\\n\\nThe PSCs were fabricated with the device configuration glass/indium tin oxide (ITO)/HTL/CH3NH3PbI3/PC61BM/Ag, where hole and electron carriers are collected by ITO and Ag electrodes, respectively. All spin-coated samples were obtained using a spin-coater (Laurell WS-650Mz-23NPP) and annealing processes were carried out using a hot plate (IKA C-MAG HP 7). Before preparation of the PSCs, each ITO-coated glass was cleaned by sonication in acetone and isopropyl alcohol, and then UV-ozone treatment was performed for 20\\u00a0min. Each Cu:NiOx layer (electrical conductivity\\u00a0=\\u00a01.1\\u00a0\\u00d7\\u00a010\\u22124\\u00a0S\\u00a0cm\\u22121, thickness \\u223c50\\u00a0nm) was prepared using sol-gel solution process followed by annealing at 500\\u00a0\\u00b0C for 30\\u00a0min . PhNa-1T (5\\u00a0mg\\u00a0mL\\u22121 in 1:1 v/v deionized water/isopropyl alcohol) was spin-coated onto the Cu:NiOx layer, followed by annealing at 100\\u00a0\\u00b0C for 10\\u00a0min. PhNa-1T layer showed a good solvent resistance against the processing solvent for deposition of the perovskite layer, as evidenced by no significant change in UV\\u2212Vis absorption spectra of the PhNa-1T film before and after washing with the N,N-dimethylformamide/dimethyl sulfoxide mixed processing solvent (Fig. S3). CH3NH3PbI3 perovskite layers were prepared using the one-step deposition method reported by Park group . 461\\u00a0mg of PbI2 and 159\\u00a0mg of CH3NH3I were dissolved in 78\\u00a0mg of dimethyl sulfoxide and 600\\u00a0mg of N,N-dimethylformamide mixed solvent. The precursor solution was sequentially spun on HTL at 1000\\u00a0rpm for 5\\u00a0s and 4000\\u00a0rpm for 15\\u00a0s while 0.5\\u00a0mL of diethyl ether was dripped onto the substrate before the change of surface color. The deposited film was then thermally annealed at 100\\u00a0\\u00b0C for 2\\u00a0min to form a dark CH3NH3PbI3 perovskite film. A PC61BM solution (20\\u00a0mg\\u00a0mL\\u22121 in chlorobenzene) was spin-coated onto each perovskite layer at 1500\\u00a0rpm for 40\\u00a0s. Finally, an Ag electrode with a thickness of 120\\u00a0nm was deposited by performing thermal evaporation under vacuum (<10\\u22126\\u00a0Torr). The active area of each cell was approx. 0.12\\u00a0cm2.\\n\\nThe surface morphologies of the HTLs were investigated by using atomic force microscopy (AFM, XE-100, Park Systems) in the non-contact mode. The I\\u2212V curves of the HTL films were obtained with linear sweep voltammetry. The energy levels of the HTLs were characterized by performing ultraviolet photoelectron spectroscopy (UPS, PHI 5000, ULVAC). X-Ray diffraction (XRD) patterns were recorded with an X-ray diffractometer (D/max PC/2500/). Field-emission scanning electron microscopy (FE-SEM, Hitachi S-4300) was utilized to determine the grain sizes of the perovskite films. Steady-state photoluminescence (PL) was recorded by using a Fluorolog3 photoluminescence spectrometer system with a monochromator (iHR320, HORIBA Scientific, excitation wavelength\\u00a0=\\u00a0460\\u00a0nm). Time-resolved photoluminescence (TR-PL) was measured with a time-correlated single photon counting (TCSPC) module (MPD-PDM Series). The current density\\u2212voltage (J\\u2212V) characteristics were investigated by using a Keithley model 2400 source measurement unit and a solar simulator equipped with a 1000\\u00a0W xenon lamp (Yamashita Denso, YSS-50S). To adjust the light intensity to the AM 1.5G 1 sun condition (100\\u00a0mW\\u00a0cm\\u22122), a Si solar cell calibrated by the National Renewable Energy Laboratory (NREL) was utilized. The external quantum efficiencies (EQEs) of the PSCs were obtained as functions of wavelength with incident photon-to-current conversion equipment (PV Measurements Inc.). The impedance analyses of the PSCs were performed by using a Solartron 1287 potentiostat and a Solartron 1260 frequency-response detector. A UV\\u2212Vis spectrophotometer (Perkin Elmer, Lambda 35) was used to obtain the absorption and transmittance spectra.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: NiO-c | PhNa-1T,\\n HTL_additives_compounds: Cu | Unknown,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I (MAI) was synthesized by the reported method []. PbI2 (99.9985%) Dimethyl sulfoxide (DMSO) (\\u226599.9%), 4-Hydroxybutyric acid lactone (GBL) (\\u226599.9%) and Li2SiO3 were bought from Sigma-Aldrich, Aladdin and Alfa Aesar, respectively. 2, 2\\u2032, 7, 7\\u2032- Tetrakis (N,N-di-p-methoxyphenylamine) \\u2013 9, 9\\u2032-spirobifluorene (Spiro-OMeTAD) was obtained from the company of Feiming in Shengzhen. FTO (15\\u202f\\u03a9/square) substrate was purchased from Asahi Glass Company Limited of Japan.\\n\\nAs shown in Fig. 1 a, the PSCs with the structure of FTO/TiO2 or LS-TiO2/CH3NH3PbI3/Spiro-OMeTAD/Ag have been fabricated. Firstly, FTO substrates were ultrasonically cleaned with deionized water, acetone, isopropanol and ethanol successively, and dried with nitrogen (N2) flow. After oxygen UV treatments for 15\\u202fmin, the cleaned FTO substrates were immersed in a TiCl4 solution (200\\u202fmM) in a closed vessel at 70\\u202f\\u00b0C for 1\\u202fh. After washed with deionized water and ethanol, the films were dried with N2 flow and annealed at 200\\u202f\\u00b0C for 30\\u202fmin in air. Then the TiO2/FTO electrodes were soaked in the Li2SiO3 aqueous solutions (concentration varies from 0 to 5\\u202f\\u00d7\\u202f10\\u22121\\u202fM) for different time (0\\u20135min) to fabricate LS-TiO2 films. Next, the obtained films were rinsed with deionized water and ethanol, then dried at 65\\u202f\\u00b0C for 10\\u202fmin to produce modified LS-TiO2. For the reference sample, the TiO2 films were not treated with Li2SiO3 aqueous solution. CH3NH3I and PbI2 with a molar ratio of 1:1 were dissolved in a mixed solution with DMSO and GBL (volume ratio of DMSO and GBL was 3:7) to obtain a 40% perovskite precursor solution in weight ratio. After the reference and LS-TiO2 films were treated with oxygen UV for 10\\u202fmin, perovskite precursor solution was spin-coated onto them at a speed 4000\\u202frpm for 40\\u202fs in the glove box. The chlorobenzene solution was dropped on the as-spun perovskite films during spin-coating at 20\\u202fs, respectively. Then, the perovskite films were annealed at 100\\u202f\\u00b0C for 10\\u202fmin immediately. After annealing, a thin layer of Spiro-OMeTAD was deposited on the perovskite layer by spin-coating a chlorobenzene solution containing 80\\u202fmM Spiro-OMeTAD, 64\\u202fmM tert-butylpyridine (TBP) and 24\\u202fmM Li-bis(trifluoromethanesulfonyl)-imide (Li-TFSI) (520\\u202fmg/ml in acetonitrile) at 5000\\u202frpm for 30\\u202fs. These samples were left in dry air overnight in the dark. Ultimately, silver (Ag) electrode with thickness of \\u223c100\\u202fnm was evaporated on the sample surface through a shadow mask under a vacuum of 1\\u202f\\u00d7\\u202f10\\u22124\\u202fPa. The sample size was 0.045\\u202fcm2.\\n\\nThe X-ray photoelectron spectroscopy (XPS) was measured by Al K-Alpha X-ray photoelectron spectrometer (Thermo Fisher Scientific, UK). The amount of Li2SiO3 introduced onto the TiO2 layer was measured using inductively coupled plasma mass spectrometry (ICP/MS, SPECTRO ARCOS MV). The photovoltaic performance of PSCs was characterized using Keithley 2420 meter under an illumination of 100\\u202fmW/cm2 (Newport 91160, 150\\u202fW solar simulator equipped with an AM 1.5\\u202fG filter). The radiation intensity was calibrated by a standard silicon solar cell (certified by NREL) as the reference. Contact angle was measures by video-based optical contact angle measurement instrument (Dataphysics OCA Pro 15, Germany). The morphology of the perovskite films was characterized by SEM (ZEISS ULTRA 55). Atomic Force Microscopy (AFM) (Asylum Research Cypher) was employed to investigate the film surface morphology, conductivity and surface potentials. The thickness of ETLs was performed by a profilometer (Dektak XT). The external quantum efficiency (EQE) was measured using EQE system (Newport 66902). The UV\\u2013vis absorption spectra of the perovskite films were measured by SHIMADZU UV-2550 spectrophotometer. The EIS was performed on the Zahner Zennium electrochemical workstation under 100\\u202fW/m2 white LED light. For the EIS measurements, a 20\\u202fmV ac-sinusoidal signal source was employed over the constant bias with the frequency ranging from 1\\u202fHz to 1\\u202fMHz. The PL spectra were measured by a fluorescence spectrophotometer (HITACHI F-5000) exited at 515\\u202fnm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Hydrothermal,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.045,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials. Formamidine iodine (FAI), spiro-MeOTAD, Ag and FTO (F:SnO2, 8\\u03a9/sq) substrate are purchased from OPV Tech Co., Ltd. All other reagents are purchased from Aladdin Biochemical Technology Co., Ltd. All chemicals were used without any further purification.\\nSynthesis of Pyrrole-modified C60 fullerenes (Pyr-fullerene). Pyr-fullerenes were synthesized by in situ chemical oxidative of pyrrole monomer on fullerene (C60) powders. At room temperature, 0.2\\u202fg fullerene powder was dispersed in 200\\u202fmL deionized water under ultrasonic vibrations for 1\\u202fh. Pyrrole in ethanol (v: v\\u202f=\\u202f1:50, 20\\u202fmL) was slowly added to the above suspension and stirred for 30\\u202fmin. Then 60\\u202fmL of 30% H2O2 aqueous solution was added dropwise to the stirred suspension and stirring was continued for 5\\u202fh at room temperature with constant mechanical stirring. The precipitated Pyr-fullerene was then filtered and rinsed several times with DI water and absolute ethanol until the filtrate became colorless. The obtained black powder was vacuum-dried at room temperature overnight.\\nPerovskite-Pyr-fullerene (PPF) bulk heterojunction (BHJ) solution preparation. Organic-inorganic hybrid perovskite (PVSK) FA0.83Cs0.17Pb(I0.83Br0.17)3 precursor solution was prepared by dissolving stoichiometric FAI, CsBr, PbI2 and PbBr2 in DMSO-DMF solution (dimethylsulfoxide and N,N-dimethylformamide, v:v\\u202f=\\u202f1:4). The solution was filtered by syringe filter (0.45\\u202f\\u03bcm, JinTeng). For BHJ solution, 1, 2, 3, 4, 5\\u202fmg/ml pyr-fullerene is mixed into perovskite solution (named PPF1, PPF2, PPF3, PPF4 and PPF5 respectively). Specifically, pyr-fullerene can be dissolved into DMF first, and then mixed with perovskite solution before spin-coating.\\nPPF based BHJ devices fabrication. Perovskite solar cells (PSCs) with a configuration of FTO/cTiO2/PPF/HTM/Ag were fabricated as following process. The compact TiO2 layer (i.e., blocking layer, cTiO2 or BL for short) were grown on patterned and cleaned FTO glasses by spin-coating a weak acidic solution of titanium isopropoxide in ethanol at 2000\\u202frpm for 30s, and annealed at 500\\u202f\\u00b0C for 30\\u202fmin. Then one-step solution method was used to deposit PPF films. Specifically, PPF precursor solution was spin-coated on 70\\u00b0Cpreheated substrate at 3000\\u202frpm for 30s, and the solution-coated substrate was vertically dipped in an anhydrous diethylether bath immediately. The substrate was kept immersed until a brown film formed in 1\\u20132\\u202fmin. Subsequently, the substrate was then taken out of the bath and heat-treated at 70\\u202f\\u00b0C for 2\\u202fmin and 130\\u202f\\u00b0C for 5\\u202fmin. After that, samples were coated with HTM by spin-coating spiro-MeOTAD solution (68\\u202fmM spiro-MeOTAD, 55\\u202fmM tert-butylpyridine (TBP) and 9\\u202fmM lithium bis (trifluoromethanesulfonyl) imide (Li-TFSI) in 1\\u202fmL chlorobenzene) at 4000\\u202frpm for 30\\u202fs. At the end, cells were left in the dark in air overnight prior to thermal evaporation Ag contact electrodes through a shadow mask to complete the solar cells fabrication.\\nCharacterization. X-ray diffraction (XRD) patterns were recorded on a Philips Rigaku D/Max-kA diffractometer with Cu K\\u03b1 radiation. Solid nuclear magnetic 1HNMR and 13CNMR (Bruker advance 600), mass spectrometry (Bruker autoflex III), and XPS (ESCALAB 250Xi) tests were used to analyze the molecular structure of the material. Morphologies and microstructures were observed with a field-emission scanning electron microscopy (FESEM, Hitachi SU-70). The Fourier transform infrared spectra (FTIR, Thermo Nicolet NEXUS 670) were used to measure the surface functional group of the films. Raman spectroscopy tests were performed on LabRAM HR Evolution. The energy levels were recorded by ultraviolet photoelectron spectrum (UPS, AXIS ULTRA DLD). UV\\u2013visible absorption spectra were collected on a spectrophotometer (TU-1901). The steady-state photoluminescence (SSPL) and time-resolved photoluminescence (TRPL) measurement were carried by FLS920 all functional fluorescence spectrometer (Edinburgh) with excitation wavelength 450\\u202fnm. The carrier concentration and mobility were performed using the MMR K2500 Hall effect test system. Admittance spectroscopy was tested with a potentiostat impedance analyzer (Agilent HP4294A) in dark. (40\\u202fHz to 1\\u202fMHz, VAC\\u202f\\u2248\\u202f0.03\\u202fV, 253\\u2013333\\u202fK, VDC\\u202f=\\u202f0\\u202fV) Capacitance-voltage measurements were carried out at 1\\u202fkHz with AC bias 0\\u20131.5\\u202fV. Photocurrent-voltage (J-V) measurements were carried out using a Keithley 2440 Source meter with Scan velocity\\u202f=\\u202f100\\u202fmV/s under AM1.5G illumination (100\\u202fmW\\u202fcm\\u22122) from a solar simulator (Newport, Class 3A, 94023A). The solar cells measured were masked with a metal aperture to define the active area to be around 0.09\\u202fcm2. The External quantum efficiency (EQE) was measured using a power source (Newport 300\\u202fW xenon lamp, 66920) with a monochromator (Newport Cornerstone 260), a multimete (Keithley 2400) and a calibrated Si-reference cell certified by the NREL. The electrochemical impedance spectroscopy (EIS) was acquired with a Princeton Parstate2273A under 1 sun light and fitted with the software Zview. The applied voltage has amplitude of 5\\u202fmV with a frequency from 1\\u202fMHz to 0.1\\u202fHz. All tests were performed in the air.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.17FA0.83PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70,\\n Perovskite_deposition_thermal_annealing_time: 2,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Most of the chemicals were purchased from TCI or Sigma Aldrich and used as received, unless specifically mentioned. Methylammonium bromide (MABr) and formamidinium iodide (FAI) salts were obtained from Xi'an Polymer Light Technology Corp, China. Spiro-OMeTAD was supplied by Luminescence Technology Corp, Taiwan, China.\\n\\nOleate-capped and monodispersed \\u03b2-NaYF4:Yb3+/Er3+/Sc3+ nanoparticles were synthesized according to the literature []. Relevant solution of lanthanide complexes (1\\u202fM) were prepared by dissolving the particular lanthanide hydrochloride in deionized water with an ultrasonic cleaning bath. In a typical procedure, 5\\u202fmL of aqueous solution containing YCl3, YbCl3, ErCl3 and ScCl3 (lanthanide ion molar ratio, Y3+/Yb3+/Er3+/Sc3+ = (78%\\u2212x)/20%/2%/x, x\\u202f=\\u202f0%, 2%, 4%, 8% and 16%) mixed with 30\\u202fmL of oleic acid (OA, AR, Aladdin) and 75\\u202fmL of 1-octadecene (ODE, AR, Aladdin) were added into a 250\\u202fmL three-necked \\ufb02ask under stirring. The mixture was heated to 160\\u202f\\u00b0C for 60\\u202fmin under an Ar atmosphere to form a bright yellow transparent solution, and then cooled down gradually to 50\\u202f\\u00b0C. Afterwards, 40\\u202fmL of methanol (purity\\u202f\\u2265\\u202f99.9%, Aladdin) solution containing 0.5\\u202fg of NaOH (purity 98%, Aladdin) and 0.74\\u202fg of NH4F (purity 99.99%, Aladdin) was added drop by drop in the \\ufb02ask and keep the reaction at 50\\u202f\\u00b0C for 30\\u202fmin. After that, the solution was heated at 70\\u202f\\u00b0C for 30\\u202fmin to remosve the methanol solvent. Then the system is heated up to 310\\u202f\\u00b0C at a heating rate of 15\\u202f\\u00b0C\\u00b7min\\u22121 and kept the temperature for 60\\u202fmin in the flowing of the argon. Finally, the mixture was cooled down rapidly to room temperature and the product was collected by centrifugation and washed with ethanol/cyclohexane several times to remove possible remnants. Thus the core of \\u03b2-NaYF4:Yb3+/Er3+/Sc3+ nanoparticles was synthesized.\\nFor the synthesis of NaYF4 shell, the steps are the same as those for \\u03b2-NaYF4:Yb3+/Er3+/Sc3+ core, except replacing 5\\u202fmL of the mixture of lanthanide hydrochlorides by YCl3 aqueous solution alone and slowly dropping 25\\u202fmL of cyclohexane solution of the obtained core particles (0.1\\u202fmol\\u202fL\\u22121) into the reaction flask before NaOH and NH4F methanol solution was added.\\nThe \\u03b2-NaYF4:Yb3+/Er3+/Sc3+@NaYF4 nanoparticles were obtained by acid treatment []. The resulting oleate-capped \\u03b2-NaYF4:Yb3+/Er3+/Sc3+ and \\u03b2-NaYF4 product (1\\u202fmmol) was dispersed in 40\\u202fmL of acidic ethanol solution (pH\\u202f=\\u202f1) adjusted with concentrated hydrochloric acid and ultrasonicated for 1\\u202fh to remove the surface ligands. Afterwards the UCNPs were collected by centrifugation at 13000\\u202frpm and washed with distilled water several times, and then re-dispersed in absolute ethanol.\\n\\n\\u03b2-NaYF4:Yb3+/Er3+/Sc3+@NaYF4 UCNPs were mixed with the commercial TiO2 paste (Dyesol 30NRT, Dyesol) for preparing the mesoporous layer of PSCs. Brie\\ufb02y, a concentration of 1\\u202fmol\\u202fL\\u22121 UCNPs ethanol solution was prepared by dispersing 1\\u202fmmol of \\u03b2-NaYF4:Yb3+/Er3+/Sc3+@NaYF4 UCNPs into 1\\u202fmL of absolute ethanol. Then the solution was mixed with the commercial TiO2 paste corresponding different mass-fractions respect to TiO2 varying from Y\\u202f=\\u202f15%\\u2013100%. The mixtures were diluted in different amount of absolute ethanol to keep the concentration of 0.1\\u202fg\\u202fmL\\u22121, and then ultrasonicated and stirred overnight. For clarity, PSC devices based on di\\ufb00erent mass ratio of UCNPs/TiO2 mesoporous layer are denoted as the pristine cell and NYES-Y cells (where Y is the mass-fraction of UCNPs ranging from 15 to 100), respectively.\\n\\nThe laser-patterned FTO (15 Ohm\\u00b7sq\\u22121, NPG, Japan) glass with size of 1.5\\u202f\\u00d7\\u202f1.5\\u202fcm2 were consecutively cleaned by detergent and sonicated in isopropanol, acetone, distilled water and ethanol and finally treated with UV-ozone for 30\\u202fmin. A compact TiO2 layer with thickness about 40\\u202fnm was prepared by spin-coating 0.15\\u202fM titanium diisopropoxide bis (acetylacetonate) (75\\u202fwt% in isopropanol, Aldrich) in a 1-butanol (99.8%, Aldrich) solution onto the substrate at 2500\\u202frpm for 30\\u202fs, and then annealed at 500\\u202f\\u00b0C for 30\\u202fmin. A scaffold layer about 150\\u2013200\\u202fnm with different UCNPs/TiO2 weight ratios was prepared by spin coating mixed paste at 2000\\u202frpm for 30\\u202fs and then annealed at 500\\u202f\\u00b0C for 30\\u202fmin.\\nCesium-containing triple cation perovskite (FA0.83MA0.17)0.95Cs0.05Pb(I0.9Br0.1)3 was synthesized by using one-step spin-coating procedure [,,]. Brie\\ufb02y, a perovskite precursor solution containing 171.9\\u202fmg of FAI, 507.1\\u202fmg of PbI2, 21.32\\u202fmg of MABr and 76.67\\u202fmg of PbBr2 was prepared in a mixed solvent of DMF and DMSO totally 950\\u202f\\u03bcL with a volume ratio of 4:1. Then 50\\u202f\\u03bcL of CsI solution in DMSO (1.5\\u202fM) was added into the mixed perovskite precursor solution to achieve the desired triple cation composition. The precursor solution was spin-coated at 1000\\u202frpm for 10\\u202fs and then at 6000\\u202frpm for 20\\u202fs. During the second step, 130\\u202f\\u03bcL of chlorobenzene was poured on the spinning substrate 5\\u202fs prior to the end of the program to rinse out residual DMSO and DMF in the precursor films. The substrate was then annealed at 100\\u202f\\u00b0C for 60\\u202fmin on a hotplate to form crystalline triple cation perovskite layers.\\nAfterwards, the spiro-OMeTAD layers were subsequently deposited on top of the as-prepared triple cation perovskite layers by spin-coating 20\\u202f\\u03bcL of chlorobenzene solution contained 72.3\\u202fmg of spiro-OMeTAD, 1\\u202fmL of chlorobenzene, 28.8\\u202f\\u03bcL of 4-tert-butyl pyridine and 17.5\\u202f\\u03bcL of bis (tri\\ufb02uoromethane) sulfonimide lithium salt (520\\u202fmg\\u202fmL\\u22121 in acetonitrile) at 4000\\u202frpm for 30\\u202fs. Finally, about 100-nm-thick Au electrodes were thermally evaporated on the spiro-OMeTAD layers under high vacuum through a shadow mask. Thus the PSCs with the active area of 0.1\\u202fcm2 (0.25\\u202f\\u00d7\\u202f0.4\\u202fcm2) were prepared.\\n\\nThe crystal structures of samples were determined by powder X-ray diffraction (XRD, Smart Lab, Rigaku) using graphite monochromatic copper radiation (\\u03bb\\u202f=\\u202f1.5418\\u202f\\u00c5). The morphologies characterizations were performed on the \\ufb01eld emission scanning electron microscopy (FE-SEM, SU8000, Hitachi) and a JEOL JEM-2100 transmission electron microscopy (TEM). The UC luminescence and was measured via the FLS 980E spectrometer (Edinburgh Instruments Ltd., UK), in which the excitation light source is a 980\\u202fnm laser. The transmittance, reflection and absorption spectra of the samples were recorded on a UV\\u2013Vis\\u2013NIR spectrophotometer (Lambda 950, PerkinElmer). The current density-voltage (J-V) characteristic curves of PSCs were recorded with a Keithley 2400 source-measure unit under 100\\u202fmW\\u202fcm\\u22122 (AM 1.5\\u202fG) illumination provided by a solar light simulator (Newport Oriel Sol 3A class, USA, calibrated by a Newport reference cell) with pre sweep delay of 0.04\\u202fs, max reverse bias of 0.1\\u202fV, max forward bias of 2.0\\u202fV, dwell time of 30\\u202fms in ambient environment. Average photovoltaic parameters of the each proposed PSC sample were obtained from 20 devices to check the reproducibility. The steady-state photoluminescence (PL) spectra was acquired using a fluorescence spectrophotometer (Lumina, ThermoFisher) equipped with a Xenon lamp at an excitation wavelength of 507\\u202fnm. The incident-photo-to-current conversion efficiency (IPCE) curves were measured as a function of wavelength from 300\\u202fnm to 1100\\u202fnm using the Newport incident photo-to-electron conversion ef\\ufb01ciency (IPCE) system (Newport, USA). The NIR response of the PSC devices was tested using a 980\\u202fnm laser with a power of 200\\u202fmW (MDL-III-980L, CNI). The stabilized current density and power output were recorded close to the maximum power point, which was extracted from the J-V curves. The electrochemical impedance spectroscopy (EIS) measurements were conducted on a Zennium electrochemical workstation (IM6) under AM 1.5G with the frequencies from 100\\u202fmHz to 1\\u202fMHz, the bias of 0\\u202fV and the amplitude of 20\\u202fmV. Long-term stability under persistent moisture was tested by XRD measurement for 7 days and record of time-dependent photovoltaic performances for 400\\u202fh under ambient condition with 40% RH and 25\\u202f\\u00b0C without encapsulation. All the average values of sample were obtained from 8 devices.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.3I2.7,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials and solvents like N,N-Dimethylformamide (DMF 99.8%), chlorobenzene, quadrol, ethylene glycol, isopropanol, Nickel (II) nitrate hexahydrate (99.9%), Zinc nitrate hexahydrate (99.9%), and Poly(acrylic acid) (PAA, Mw 1800) were purchased from Sigma-Aldrich and used as received. Methylammonium iodide (CH3NH3I\\u202f\\u2265\\u202f99.5%), Lead iodide (PbI2 99.99%), and PC61BM (99.5%) were purchased from Xi'an Polymer Light Technology Corp. China. Bathocuproine (BCP, 98%) were purchased from Aladdin. For the Zn-doped NiOx precursor solution, zinc nitrate hexahydrate (5%) was mixed with Ni(NO3)2\\u00b76H2O and dissolved in ethylene glycol solution containing ethylenediamine (Sigma Aldrich). The NiOx:Zn films exhibit morphology uniformity, high transparence, and enhanced conductivity compared with pure NiOx films, which can be referred to our previous work [].\\n\\nThe perovskite photovoltaic device had a planar structure of FTO/NiOx:Zn/MAPbI3/[,]-phenyl-C61-butyric acid methyl ester (PC61BM)/bathocuproine (BCP)/Ag. Fluorine-doped tin oxide (FTO) coated glass substrates were washed successively with deionized water, acetone. After that, the etched and cleaned FTO glass were dried in nitrogen \\ufb02ow and treated by UV-ozone for 15\\u202fmin for device fabrication. The zinc doped NiOx precursor solution was spin-coated onto FTO substrate at a speed of 5000\\u202frpm for 40\\u202fs and then post-annealed at 400\\u202f\\u00b0C in ambient air for 60\\u202fmin [,]. To form a MAPbI3 perovskite precursor (1\\u202fM), an equimolar ratio of PbI2 and MAI was dissolved in DMF with different amounts of Poly(acrylic acid) (PAA). The bladed coating of perovskite films was deposited in an N2-purged glovebox (below 0.1\\u202fppm O2 and H2O). In the doctor-blade coating process, the perovskite precursor solution was dripped onto the FTO glass on a hot plate set at 150\\u202f\\u00b0C, then the glass blade swiped linearly at a speed about 1.5\\u202fcm\\u202fs\\u22121. After blading, the substrates were quickly removed from the hot plate and annealed at 100\\u202f\\u00b0C in N2-purged glovebox for 10\\u202fmin. We used 10\\u202f\\u03bcL of precursor solution per 2.25\\u202fcm2 substrate. This was much less than 20\\u201350\\u202f\\u03bcL typically used for spin coating of similar perovskite solutions over the same area substrate, which demonstrated the advantages of efficient material usage by doctor-blade coating. The PCBM layer was spin-coated at 3000\\u202frpm for 30\\u202fs from chlorobenzene with a concentration of 20\\u202fmg\\u202fmL\\u22121, and then the BCP (0.5\\u202fmg\\u202fmL\\u22121 in IPA) layer was spin-coated at 4000\\u202frpm for 30\\u202fs on the PCBM film. Finally, 70\\u202fnm Ag was deposited at speed of 1\\u202f\\u00c5\\u202fs\\u22121 with a mask in a vacuum deposition chamber under a high vacuum of 5\\u202f\\u00d7\\u202f10\\u22124\\u202fPa.\\n\\nThe film morphology and composition were characterized by scanning electron microscope (SEM, QUANTA FEG250) and atomic force microscope (AFM, MFP-3D-Stand Alone, Asylum Research). The X-ray diffraction patterns were recorded at a scan rate of 10\\u00b0 min\\u22121 on Rigaku Ultima IV X-ray diffractometer with Cu K\\u03b1 radiation (0.15406\\u202fnm). The photoluminescence (PL) signal dispersed by a monochrometer was detected by a photomultiplier (PMTH-S1-CR131) through a lock-in amplifier (SR 830). For time-resolved PL (TRPL) spectra measurements, a 405\\u202fnm nanosencond diode laser was used as excitation source. The optical absorption spectra were examined by a UV\\u2013vis\\u2013NIR spectrophotometer (UV-3600, Shimadzu). The Fourier Transform infrared (FT-IR) spectroscopy (Nicolet iS50) was used to analyze the perovskite films. Raman spectra were measured by a Horiba spectrometer (LabRAM HR Evolution) using an Nd: YAG laser beam at the excitation wavelength of 532\\u202fnm. Current-voltage (J-V) characteristics of solar cells were measured using a Keithley 2612 source measure unit under a simulated AM 1.5G spectrum (100\\u202fmW\\u202fcm\\u22122)\\u202fby a solar simulator (San-Ei, 3A, 150\\u202fW) with different scanning directions. The J-V measurement was performed in the ambient air with a humidity of around 40%, and the device area is 0.14\\u202fcm2, which is defined by the cross section of Ag and FTO. The external quantum efficiency (EQE) was measured with a QEX10 system (PV Measurement).\\n\\nFemtosecond transient absorption was detected using a pump\\u2013probe method to measure differential absorption (\\u0394OD) spectra and their decay profile. Laser pulses (800\\u202fnm, 50 fs pulse length, 1\\u202fkHz repetition rate) were generated by a Ti:sapphire femtosecond laser (Hurricane, Spectra-Physics) source. An optical parametric amplifier was used to change the laser wavelength. The pump pulses at 560\\u202fnm were generated by a 1-mm-thick BBO crystal as a second harmonic of the laser. Pump power was carefully controlled by a neutral density filter (4\\u202f\\u03bcJ\\u202fcm\\u22122 per pulse in front of glass side) to minimize the effect of carrier annihilation or non-geminate recombination. For the white light continuum (WLC) probe pulses we used the super-continuum generation from a thin sapphire window (3\\u202fmm in thickness). The time delay between pump and probe was carefully controlled in such a way that the pump beam travels along a variable optical delay. A chopper was used to block every other pump pulse, and each probe pulse was measured by a charge-coupled device (CCD) after dispersion by a grating spectrograph. The polarization angle between pump and probe beams was set to the magic angle (54.7\\u00b0) by placing a Berek compensator in the pump beam. The kinetic of the different scans stay the same showing no sign of degradation. Excitation power and spot size measurements were used to determine the excitation fluence.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: NiO-c,\\n ETL_additives_compounds: Zn,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: PAA,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Doctor blading,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PCBM-60 | BCP,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.14,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"FTO (NSG TECTM 8.8\\u202f\\u03a9/sq) coated glass was cut into pieces of 2\\u202f\\u00d7\\u202f2\\u202fcm2 in size and partially etched with zinc powder and hydrochloric acid. The substrates were thoroughly cleaned with acetone, deionized (DI) water, and ethanol for 15\\u202fmin, sequentially. UV-ozone was used to remove organic residue on the FTO. A TiO2 blocking layer (bl-TiO2) was spin-coated onto the FTO substrate at 4000\\u202frpm for 30\\u202fs using a prepared 0.15\\u202fM titanium diisopropoxide bis-(acetylacetonate) in 1-butanol followed by annealing in a box furnace at 500\\u202f\\u00b0C for 30\\u202fmin. The substrate was immersed in an aqueous TiCl4 solution for 30\\u202fmin\\u202fat 72\\u202f\\u00b0C and annealed in the box furnace at 500\\u202f\\u00b0C for 30\\u202fmin. Mesoporous-TiO2 nanoparticles diluted in a TiO2 paste in ethanol (1:5.5\\u202fwt%, Sharechem) were spin-coated onto the bl-TiO2/FTO substrate at 5000\\u202frpm for 30\\u202fs followed by annealing at 550\\u202f\\u00b0C for 30\\u202fmin. After cooling to room temperature, a CH3NH3PbI3 perovskite layer was formed on the TiCl4 treated mesoporous TiO2 layer in a one-step manner using an adduct method. To prepare the CH3NH3PbI3 solution, PbI2, CH3NH3I, and DMSO (1:1:1: M ratio) were dissolved in a N,N-dimethylforDMDide (DMF) solvent for 30\\u202fmin and spin-coated at 4000\\u202frpm for 25\\u202fs, and diethyl ether was then dropped during the spin-coating procedure. The substrate was then annealed at 65\\u202f\\u00b0C for 3\\u202fmin and at 100\\u202f\\u00b0C for 10\\u202fmin. The HTL solution was prepared by dissolving 36\\u202fmg of 2,2\\u2032,7,7\\u2032-tetrakis[N,N-di(4-methoxyphenyl)-amino]-9,9\\u2032-spirobi-fluorene (spiro-OMeTAD) in 500\\u202f\\u03bcL of chlorobenzene, 14.4\\u202f\\u03bcL of 4-tert-butyl pyridine, and 8.8\\u202f\\u03bcL of lithium-bis(trifluoro-methanesulfonyl)-imide (Li-TFSI) in acetonitrile (720\\u202fmg\\u202fml\\u22121). The solution was spin-coated on the perovskite/mp-TiO2/bl-TiO2/FTO at 4000\\u202frpm for 30\\u202fs. Finally, a 20-nm-thick MoOx, 7-nm-thick Ag, and 20-nm-thick MoOx were deposited using e-beam evaporation on the top of the HTL as a transparent top electrode.\\n\\nThe thin TiO2 as an ETL was prepared using a thermal oxidation process on a Ti metal plate, as previously reported in our group []. Ti metal plates were cleaned in aceton, deionized water, and ethanol for 20\\u202fmin separately. After cleaning, Ti metal plates were annealed at 500\\u202f\\u00b0C for 24\\u202fh. The oxidized TiO2 was then annealed at 400\\u202f\\u00b0C for 1\\u202fh to control the oxygen vacancies on the surface of the TiO2.\\n\\nThe results of the light-soaking PSC stability test and the photovoltaic performance of the devices with a metallic mask (active area 0.14\\u202fcm2) were measured under solar-simulated light (Oriel Sol 3A class AAA, Newport) using an electrochemical workstation (CHI660, CHI Instrument) system. The AM 1.5\\u202fG sun light (100\\u202fmA\\u202fcm\\u22122) was calibrated to a reference Si solar cell (PVM 95). The cross-sectional structures and individual layers of the devices were obtained using a field-emission scanning electron microscope (JSM-7600F, JEOL). The incident photo-to-current conversion efficiency and integrated current of the PSCs were measured through quantum efficiency measurements within a spectra range of 300\\u2013800\\u202fnm in air under light illumination from a 300\\u202fW xenon lamp. The transmittance of the MoOx/Ag/MoOx films was examined using a PerkinElmer Lambda 35 UV/vis spectrometer equipped with an integrating sphere. The phase structure of the device was confirmed using X-ray diffraction (PANanalytical Empyrean). The angle ranged from 10\\u00b0 to 40\\u00b0 with a 2\\u03b8 range. Defects in the PSCs were measured using admittance spectroscopy (AS) at an AC voltage of 30\\u202fmV. The frequency and temperature were applied within a frequency sweep ranging from 102 to 106\\u202fHz, and within a temperature range of 170\\u202f\\u00b0C\\u2013290\\u202f\\u00b0C.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65,\\n Perovskite_deposition_thermal_annealing_time: 3,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoOx | Ag | MoOx,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.14,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Synthesis and Fabrication of ETLs: For the TiO2 solution, 60\\u202f\\u03bcL of HCl (37%) and 738\\u202f\\u03bcL of titanium (IV) isopropoxide (99.999%) solutions were dissolved in 8\\u202fmL of anhydrous ethanol. After that, to make a denser TiO2 film, 120\\u202fmM of titanium (IV) chloride (99.9%, TiCl4) aqueous solution was prepared by the additional dip-coating process for 30\\u202fmin, followed by calcination at 500\\u202f\\u00b0C for 30\\u202fmin. To synthesize the ZnO sol\\u2013gel solution, 5.45\\u202fM of zinc acetate dehydrate (Zn(CH3COO)2 2H2O) with 0.5\\u202fg of ethanolamine were dissolved into 2-methoxyethanol. The solution was spin-coated onto the substrate at 5,000\\u202frpm for 50\\u202fs, followed by the annealing process at 200\\u202f\\u00b0C for 30\\u202fmin. Fig. S6 and Table S2 of the SI show the results of the device performance with several annealing conditions and optimization of the ZnO layer. The interlayer solution was prepared by various concentrations of PEIE solution ((35\\u201340) wt %, Aldrich) dissolved in 2-methoxyethanol. Fig. S7 and Table S3 of the SI show the systematically optimized thickness of the PEIE layer with varying concentrations, and the surface plasmon resonance (SPR) spectrometry confirmed the nm-sized PEIE thickness. The optimized concentration (0.2\\u202fwt %) of PEIE solution was spin-coated at 5,000\\u202frpm for 50\\u202fs, followed by thermal annealing at 100\\u202f\\u00b0C for 10\\u202fmin. The optimized thickness of the PEIE layer is 3.5\\u202fnm (Fig. S7 (b)).\\nPerovskite Film Fabrication: For the one-step process, 2\\u202fM of the CH3NH3PbI3 (MAPbI3) solutions were prepared by dissolving the amount of PbI2 and MAI in the solution of \\u03b3-butyrolactone:DMSO (5:5, volume ratio) mixture, with stirring at 70\\u202f\\u00b0C. The prepared solutions were filtered by the PTFE syringe filter (0.2\\u202f\\u03bcm) and coated onto the substrate via a consecutive spin-coating process at 1,000\\u202frpm for 10\\u202fs and 5,000\\u202frpm for 60\\u202fs, respectively. During the second spin-step at 5,000\\u202frpm, 1,000\\u202f\\u03bcL of chlorobenzene was dropped onto the center of the substrate for better crystallization and uniform surface, followed by annealing at 100\\u202f\\u00b0C for 1\\u202fh. For the two-step process, on the other hand, the PbI2 was spin-coated on the substrate followed by the annealing process at 100\\u202f\\u00b0C for 5\\u202fmin while kept in the glove box. After the PbI2 layer was dried, CH3NH3I (MAI) dissolved into the isopropanol solution was spin-coated on top of the PbI2 film for 40\\u202fs\\u202fat 1500\\u202frpm to form the perovskite structure.\\nDevice Fabrication: For a reference device, FTO/glass substrates were cleaned via sequential ultrasonic treatments with acetone, isopropyl alcohol, and deionized water for 30\\u202fmin, respectively. A dense compact TiO2 electron-transport layer (ETL) was deposited onto the FTO/glass substrate. The solution was spin-coated onto the F-doped SnO2 (FTO, AMG Tech) substrate at 2,000\\u202frpm for 30\\u202fs, followed by consecutive annealing at 125\\u202f\\u00b0C for 15\\u202fmin and 500\\u202f\\u00b0C for 30\\u202fmin, respectively. The perovskite layer was then deposited onto the ETL using the aforementioned method. For deposition of the hole-transport layer, 63\\u202fmg of spiro-OMeTAD, 20\\u202f\\u03bcL of tert-butylpyridine and 70\\u202f\\u03bcL of lithium bis(trifluoromethanesulfonyl)imide (170\\u202fmg/mL in acetonitrile) were dissolved into 1\\u202fmL of chlorobenzene, followed by a spin-coating process at 4,000\\u202frpm for 30\\u202fs. Finally, 100\\u202fnm of Au film was deposited as a top electrode using a thermal evaporator system. For the flexible device, we substituted the rigid FTO/glass substrate by the ITO/PEN flexible substrate with an identical device fabrication protocol.\\nDevice characterization: The solar simulator stored in the glove box was used to measure the J\\u2013V curves with a scanning rate of 1 point per 0.05\\u202fV change from reverse bias using a Keithley 2400 instrument. The AM 1.5 (1 sun, 100 mW cm-2) solar power was supplied by a class AAA (Spectral Match: 0.75\\u20131.25, Irradiance Spatial Non-Uniformity: 2%, Temporal Instability (STI/LTI): 0.5%/2%) solar simulator and calibrated the 1 sun intensity using a silicon reference solar cell. The optical properties of the perovskite films were measured using ultraviolet\\u2013visible\\u2013near infrared spectrometry (Varian Technology, Cary 5000). To analyze the crystallinity and structure of each film, wide-angle X-ray diffraction (XRD) patterns were measured (EPLEX, SPIN-1200D). For the grazing-incidence wide-angle X-ray scattering (GIWAXS) measurement, the PLS-II 9A U-SAXS beamline at Pohang Accelerator Laboratory (Republic of Korea) was carried out. The incidence angle was set to 0.18\\u00b0, and the X-ray generating from the in-vacuum undulator (IVU) was monochromated using Si (111) double crystals (E\\u202f=\\u202f11.055\\u202fkeV, \\u03bb\\u202f=\\u202f1.121\\u202f\\u00c5). To measure the surface morphology and phase degradation, atomic force microscopy (AFM) (Veeco, Digital Instrument Dimension 3100) and scanning electron microscopy (SEM) (JEOL, JSM-6700F) were used. The incident photon-to-current conversion efficiency (IPCE) was measured (HS Technology Inc.) to analyze the incident photo-to-current efficiency of the PSC devices.\\nXPS and UPS measurement: The photoelectron spectroscopy spectra were extracted by a PHI-5000 ultrahigh vacuum surface analysis system equipped with a He discharge lamp (21.22\\u202feV) and a monochromatic Al K\\u03b1 X-ray. All spectra were measured under ultrahigh vacuum condition. (<1\\u202f\\u00d7\\u202f10\\u22126\\u202fPa). The spectra of ZnO, TiO, and ZnO with PEIE film were fabricated on FTO substrate with the different ratio. The work function (\\u03d5) was determined from the secondary cutoff region (E cutoff) and Fermi energy (E Fermi), which were clearly defined and calculated using the following equation: \\u03d5\\u202f=\\u202fh\\u03bd - E cutoff\\u00a0+\\u00a0E Fermi\\nThe valence band energy (E VB) was determined from the valence band cutoff region (E VB,cut) and the vacuum level shift (\\u0394E vac) with under layers, which were calculated using the following equation: E VB\\u00a0=\\u00a0\\u03d5\\u00a0+\\u00a0E VB,cut\\u00a0+\\u00a0\\u0394E vac where, h\\u03bd\\u202f=\\u202f21.22\\u202feV is the incoming photon energy from the He I source, and \\u22125\\u202fV bias was applied to make a clear boundary in the E cutoff region.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Zinc acetate dihydrate, methanol and Potassium hydroxide was purchased from Aldrich. Anhydrous chloroform and Anhydrous n-butanol were purchased from AcrosAll chemicals, which used as received without any further purification. These materials were used preparation ZnO nanoparticle solution. CH3NH3I, Lithium salts (>99.0%), tert-butylpyridine (tBP), Spiro-OMeTAD(2,20,7,70-tetrakis-(N,N-di-4-methoxyphenylamino)-9,90-spirobiuorene, >99.0%), and N,N-dimethyl formamide (DMF, >99.9%), Dimethyl sulfoxide (DMSO, >99.95%), chlorobenzene (>99.9%) were purchased from YouXuan Tech. Co. All the chemicals and solvents were kept in a glove-box and starting experiments.\\n\\nThe preparation process of ZnO dispersion is strictly in accordance with the method provided in Kelly et al. literature []. The X-ray diffraction pattern of as-prepared ZnO NPs was shown in Fig. S1(supporting information).\\nPatterned glass/F-doped SnO2 substrates were sequentially cleaned in deionized water, ethanol and acetone respectively with duration of 20\\u202fmin each. The ZnO dispersion filtered with a PVDF 0.45\\u202f\\u03bcm filter and spin coated on the FTO substrates at 3000\\u202frpm for 30\\u202fs, the procedure was repeated three times to obtain a continuous smooth film. The ZnO films were separated into two categories, one set of films were annealed for 1\\u202fh at 150\\u202f\\u00b0C, 200\\u202f\\u00b0C, 250\\u202f\\u00b0C, 300\\u202f\\u00b0C, 350\\u202f\\u00b0C, 400\\u202f\\u00b0C in a nitrogen filled glove-box, which was named as AT-150\\u202f\\u00b0C, AT-200\\u202f\\u00b0C, AT-250\\u202f\\u00b0C and AT-300\\u202f\\u00b0C, AT-350\\u202f\\u00b0C, AT-400\\u202f\\u00b0C. The other set of films were treated with UV-O3 for 5\\u202fmin, 10\\u202fmin, 15\\u202fmin, 20\\u202fmin and 25\\u202fmin, 30\\u202fmin which was named as UV-5min, UV-10min, UV-15min and UV-20min, UV-25min, UV-30min correspondingly. The ZnO films without any treatment is named as WT for reference. The environment humidity of ZnO ETLs processing is less than 35%.\\n\\nThe 85\\u202f\\u03bcL precursor solution of CH3NH3PbI3 (PbI2 and CH3NH3I with equimolar were dissolved in DMF and DMSO with volume ratio of 700\\u202f\\u03bcL: 300\\u202f\\u03bcL) were spin coated on the prepared ZnO film at 5000\\u202frpm. The 100\\u202f\\u03bcL anhydrous chlorobenzene was quickly dropped onto the center of the substrate at 30\\u202fs. The films were annealed at 65\\u202f\\u00b0C for 5\\u202fmin and 100\\u202f\\u00b0C for 10\\u202fmin []. A spiro-OMeTAD solution consist of 72\\u202fmg of spiro-OMeTAD, 29.5\\u202f\\u03bcL of 4-tert-butylpyridine (tBP), and 18.5\\u202f\\u03bcL of a lithium-bis (triuoromethanesulfonyl) imide (Li-TFSI) solution (520\\u202fmg Li-TFSI/1\\u202fmL acetonitrile) in 1\\u202fmL of chlorobenzene. It was spin-coated on the perovskite film with 1000\\u202frpm for 10\\u202fs and 3000\\u202frpm for 30\\u202fs. The samples were stored in the dry and dark circumstance overnight at room temperature. Finally, a 100\\u202fnm thick Ag electrode was deposited by thermal evaporation.\\nTwo series solar cells of glass/FTO/ZnO/CH3NH3PbI3/Sprio-OMeTAD/Ag have been fabricated in our case. One set of solar cells were fabricated with UV-5min, UV-10min, UV-15min and UV-20min, UV-25min, UV-30min ZnO ETLs. The other set of solar cells were fabricated with AT-150\\u202f\\u00b0C, AT-200\\u202f\\u00b0C, AT-250\\u202f\\u00b0C and AT-300\\u202f\\u00b0C, AT-350\\u202f\\u00b0C, AT-400\\u202f\\u00b0C ZnO ETLs.\\n\\nUV\\u2013Vis\\u2013NIR spectra were obtained using an UV\\u2013Vis\\u2013near-infrared (NIR) spectrophotometer (UV\\u20133101PC) equipped with the integrating sphere. The X-ray diffraction (XRD) measurements was performed on Japan Rigaku D/max-ga X-ray diffractometer with Cu K\\u0251 radiation (\\u03bb\\u202f=\\u202f1.5418\\u202f\\u00c5) at room temperature. The step size (2\\u03b8) is 0.01\\u00b0. The SEM images were acquired by a field emission scanning electron microscope (Hitachi S-4800). The steady-state photoluminescence measurements and time-resolved PL measurements (TRPL) measurements were performed on Horiba Jobin Yvon Fluorolog-3 fluorescence spectrometer. We further utilized exponential function: I(t)\\u202f=\\u202fI0exp(\\u2212(ti/\\u03c4i)\\u03b2i) to fit the decay curves, where \\u03c4i is the decay life time and \\u03b2i is a stretching parameter. Hall measurements were performed with van der Pauw configuration by Lake Shore 7704A at room temperature. The XPS measurements were carried on X-ray photoelectron spectrometer (ESCALAB MARK II, VG Inc.) with an Al K\\u03b1 monochromatized source.\\n\\nThe Keithley 2400 source meter measurement system was used to acquire the J\\u2013V characteristics of PSCs under AM 1.5\\u202fG simulated sunlight illumination (100 mWcm\\u22122, Model 91160, Oriel). The light source standard by silicon reference cell (91160V Oriel Instruments). The J\\u2013V measurement scan rate was 0.1\\u202fV-1 and delay time was 10\\u202fm. The EQE set-up (QEX10, PV Measurement) was used the spectral responses of PSCs device, during which chopping frequency was 40\\u202fHz and a lock-in amplifier was used. The EIS measurements were performed by Potentiostat Galvanostat EIS Analyzer 4000\\u202fat open circuit voltage applying 20\\u202fmV amplitude in the range of 1-1\\u202fMHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65.0; 100.0,\\n Perovskite_deposition_thermal_annealing_time: 5.0; 10.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Indium nitrate hydrate (In(NO3)3\\u00b7xH2O), phenyl-C61-butyric acid methyl ester (PCBM), Lead iodide (PbI2), Lead chloride (PbCl2) were purchased from Sigma. Spiro-OMeTAD was purchased from Xi'an P-OLED Corp. Methylammonium iodide (MAI), Formamidinium iodide (FAI) were purchased from Dyesol. All the solvent were purchased from Sigma-Aldrich. All these materials were used directly as received.\\n\\nITO (10\\u202f\\u03a9 per square) glasses were cleaned in an ultrasonic bath for 20\\u202fmin by detergent, deionized water, acetone, and ethanol, respectively. Then, the clean ITO glasses were treated in UV-ozone stove for 20\\u202fmin. The indium precursor solution was prepared by dissolving 354.8\\u202fmg In(NO3)3\\u00b7xH2O in 5\\u202fmL 2-methoxyethanol with 114\\u202f\\u03bcL NH3\\u00b7H2O and 200\\u202f\\u03bcL acetylacetone, and the mixed solution was allowed to stir for 12\\u202fh. Then the precursor solution was spin-coated onto the substrate at 3500\\u202frpm for 30\\u202fs and annealed at 150\\u2013230\\u202f\\u00b0C for 30\\u202fmin. The samples were transferred into a nitrogen-filled glove box after cooling down to room temperature. The PCBM layer was prepared by spin-coating a PCBM solution (10\\u202fmg/mL in CB) at 6000\\u202frpm for 45\\u202fs and heating at 100\\u202f\\u00b0C for 5\\u202fmin. The perovskite layer was prepared by a two-step process as our previous work []. The PbX2 solution was prepared by dissolving 1.36\\u202fM PbI2 and 0.24\\u202fM PbCl2 in DMF and stirring at 70\\u202f\\u00b0C for 2\\u202fh. The mixed organic cation solution was prepared by dissolving 70\\u202fmg MAI and 30\\u202fmg FAI in 1\\u202fmL IPA with additional 10\\u202f\\u03bcL DMF. The PbX2 solution was spin coated on the substrates at 3000\\u202frpm for 45\\u202fs, then the mixed organic cation solution was spin coated on the substrates at 3000\\u202frpm for 45\\u202fs. After that, the substrates were annealed at 100\\u202f\\u00b0C for 10\\u202fmin. Next, the hole transport layer was spin-coated onto the perovskite layer at 4000\\u202frpm for 45\\u202fs, and it consisted of 90\\u202fmg spiro-OMeTAD, 45\\u202f\\u03bcL Li-TFSI (170\\u202fmg/mL in acetonitrile), 75\\u202f\\u03bcL FK209 (100\\u202fmg/mL in acetonitrile) and 10\\u202f\\u03bcL tBP. Finally, 100\\u202fnm thick Ag electrodes were deposited as back electrodes by thermal evaporation. The device area was 0.075\\u202fcm2.\\n\\nThe current density \\u2013 voltage (J \\u2013 V) curves were obtained using a Keithley 2400 source meter unit under simulated AM 1.5\\u202fG illumination (100\\u202fmW/cm2) with a XES-70S1 solar simulator. The system was calibrated by a NREL-certified monocrystal Si photodiode detector. The external quantum efficiency (EQE) was measured by a solar cell quantum efficiency measurement system (SCS10-X150, Zolix instrument. Co. Ltd). X-ray photoelectron spectroscopy (XPS) was performed on a scanning XPS microprobe (PHI 5000 VersaProbe, Ulvac-PHI). X-ray diffraction (XRD) was tested on Bruker D8 Advance XRD. The perovskite surface morphology was measured by scanning electron microscopy (SEM) (JSM-7800F). The absorption spectra were measured on a PerkinElmer Lambda 950 spectrophotometer.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: In2O3-c | PCBM-60,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Solution combustion | Spin-coating,\\n Perovskite_composition_long_form: FA0.3MA0.7PbI3,\\n Perovskite_composition_short_form: FAMAPbI,\\n Perovskite_additives_compounds: PbCl2,\\n Perovskite_deposition_solvents: DMF | DMF; IPA,\\n Perovskite_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown | 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.075,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (CH3NH3I) was purchased from Dyesol. Spiro-OMeTAD (99.7%) was purchased from Borun New Material Technology Co., Ltd. PCBA powders (99%) were purchased from Solenne BV. All other materials were purchased from Sigma-Aldrich and used as received.\\n\\nPre-patterned indium tin oxide (ITO) coated glass substrates (PsiOTech Ltd., 15 Ohm/sqr) were cleaned sequentially with 2% hellmanex detergent, deionized water, acetone, and isopropanol, followed by 10 min oxygen plasma treatment. A ZnO sol-gel was prepared following a previously reported recipe . Doping with Cs or Li was accomplished by adding either caesium carbonate or lithium acetate to the sol-gel solution in 2% and 3% MR, respectively. These molar ratios were chosen as they yielded the most efficient devices. Immediately after plasma cleaning, ZnO solution (with or without dopants) was spin-coated at 2000 rpm for 45 s and annealed for 30 min at 200 \\u00b0C. Afterwards, the substrates were modified with a SAM of PCBA following a previously reported procedure . For the perovskite layer a lead acetate trihydrate recipe was used: CH3NH3I and Pb(Ac)2\\u00b73(H2O) (3:1, molar ratio) were dissolved in anhydrous N,N-dimethylformamide (DMF) with a concentration of 40 wt% with the addition of hypophosphorous acid solution (6 \\u00b5l / 1 ml DMF). The perovskite solution was spin-coated at 2000 rpm for 60 s in a drybox (RH < 0.5%). After drying for 5 min, the as-spun films were annealed at 80 \\u00b0C for 30 min. Subsequently, spiro-OMeTAD solution (80 mg Spiro-OMeTAD dissolved in 1 ml chlorobenzene with 17.3 \\u00b5l Li-TFSI (520 mg/ml acetonitrile) and 28.5 \\u00b5l 4-tert-butylpyridine) was spin-coated on top of the perovskite layers at 2000 rpm for 45 s. To complete the device, a 80 nm silver electrode was deposited via thermal evaporation under high vacuum.\\n\\nThe current density-voltage (J-V) measurements were performed under simulated AM 1.5 sunlight at 100 mW cm\\u22122 irradiance (Abet Sun 3000 Class AAA solar simulator) with a Keithley 2450 Source Measure Unit. The light intensity was calibrated with a Si reference cell (NIST traceable, VLSI) and corrected by measuring the spectral mismatch between the solar spectrum, the spectral response of the perovskite solar cell and the reference cell. The mismatch factor was calculated to be around 10%. The cells were scanned from forward bias to short circuit and back at a rate of 0.15 V s\\u22121 and 0.025 V s\\u22121 after holding under illumination at 1.2 V for 2 s. To eliminate the contribution of the area surrounding each pixel, a mask that covers these areas from illumination was employed.\\nFor transient photocurrent measurements, the light of an inorganic LED (Thorlabs TO-1 \\u00be, \\u03bb = 465 nm) was pulsed by a function generator (Agilent/Keysight 33510B; pulse length = 2 ms) and focused on the solar cell. The resulting photocurrent was measured with an oscilloscope (Picoscope 5443A) with a 50 \\u03a9 terminator placed across the oscilloscope input.\\n\\nZnO samples for XPS/UPS measurements were prepared as described above on ITO substrates and then transferred to the ultrahigh vacuum chamber of the XPS system (Thermo Scientific ESCALAB 250Xi). The XPS measurements were performed using a XR6 monochromated Al K\\u03b1 source (h\\u03bd = 1486.6 eV) and a pass energy of 20 eV. UPS measurements were carried out using a He discharge lamp (h\\u03bd = 21.2 eV) and a pass energy of 2 eV. Measurements were collected at three different spots for each sample. XPS depth profiling was performed using an Ar cluster source with cluster energy of 4000 eV. AFM (Bruker MultiMode) was performed in tapping mode in air with silicon tips (Bruker NTESPA) to study the surface morphology of the undoped and doped ZnO films. Layers for PDS characterisation were prepared on spectrosil in an identical fashion to those for photovoltaic devices. In the N2 glovebox the samples were placed into a sample holder filled with Fluorinert FC-770 (IoLiTec). A 150 W Xenon short-arc lamp (Ushio) provides light for a monochromator (Cornerstone 260 Oriel, FWHM 16 nm) to achieve a chopped, tunable, monochromatic pump beam. The heat caused through absorption of the pump light in the films changes the refractive index of the Fluorinert. This change is detected by deflecting a probe He-Ne-laser (REO) whose displacement in turn is measured by a position-sensitive-detector (Thorlabs, PDP90A). The magnitude of the deflection is determined by a lock-in amplifier (Amatec SR 7230) and directly correlated to the absorption of the film.\\n\\nTo study the effect of doping and surface modification of ZnO on the perovskite film formation, scanning electron microscopy was conducted using an Ultra FE-SEM Gemini Ultra 55 (Zeiss) microscope with a working distance of 3 mm and an acceleration voltage of 1.6 kV. Samples were mounted on standard SEM holders using conductive silver paste to avoid sample charging. Photoluminescence (PL) measurements were carried out inside an integrating sphere (LabSphere) with excitation by a 447 nm diode laser (Dragon Lasers). The spectra were recorded using a QE65000 (Ocean Optics) spectrometer.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-c | PCBA,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PbI2, PbBr2 (99.9985%), 4-tert-butylpyridine (TBP) and bis(trifluoromethane) sulfonimide lithium salt (LiTFSI) were purchased from Sigma-Aldrich, N, N-dimethylformamide (DMF), dimethyl sulphoxide (DMSO) and chlorobenzene (CB) were from Alfar Aesar. Methylammonium bromide (MABr) and formamidinium iodide (FAI) were from Xi\\u2019an Polymer Light Technology Corp. and caprolactam (CPL) was from Sinopharm Chemical Reagent Co., Ltd. Spiro-OMeTAD was purchased from Luminescence Technology Corp. All the chemicals were directly used without further purification. Laser-patterned FTO glass (Pilkington, thickness of 2.2 mm and sheet resistance of 15 \\u03a9 sq\\u22121) was sequentially cleaned with a mild detergent, distilled water and ethanol in an ultrasonic bath. The substrate was treated with ozone for 15 min prior to use.\\n\\nThe CPL-based precursor solution for perovskite films was prepared by dissolving 1.15 M PbI2, 0.20 M PbBr2, 1.10 M FAI, 0.20 M MABr and some CPL in pure DMF. For the control group, the precursor solution with the same concentrations of PbI2, PbBr2, FAI and MABr was prepared in DMF/DMSO mixed solvent (v: v = 4:1). Here, the amount of CPL is defined as CPL-x, x represents the CPL/PbI2 molar ratio, including CPL-0%, CPL-20%, CPL-50%, CPL-75%, CPL-100%, CPL-150. The compact TiO2 layer was deposited on the FTO glass with a 0.125 M titanium isopropoxide sol-gel precursor solution by spin coating at 3000 rmp, then sintered at 500 \\u00b0C for 1 h. Then, the TiO2 film was treated with 0.025 M TiCl4 aqueous solution for 30 min, and entered at 500 \\u00b0C for 1 h. 0.1 mg/mL [6,6]-phenyl-C61-butyric acid (PCBA) in CB was first spin-coated on the top of TiO2 compact film . Perovskite films were fabricated by anti-solvent one-step spin-coating method . In details, perovskite precursor solution was spin-coated at 1000 rpm for 10 s and subsequently at 5000 rpm for 30 s, 120 \\u00b5L CB was poured onto the spinning substrate at 9 s in the second spinning step. The half-crystallization perovskite film was heated at 170 \\u00b0C for 10 min and 100 \\u00b0C in vacuum for 30 min 200 nm-thickness spiro-OMeTAD layer was deposited onto the perovskite film at a speed of 3000 rpm and then heated for 5 min at 60 \\u00b0C on a hot plate. The precursor preparation, perovskite and spiro-OMeTAD spin-coating processes were carried out in the glove box. At last, 80 nm-thickness Au electrode was deposited via thermal evaporation under the vacuum of 10\\u22127 Torr.\\n\\nSEM images were measured by scanning electron microscopy (SEM, Hitachi S4800) under 10 kV at various magnifications. X-Ray Diffraction (XRD) patterns were measured on a Bruker X-ray diffractometer using Cu K\\u03b1 as the radiation source. UV\\u2013vis absorption spectra were obtained on Shimadzu UV-2550 in the wavelength range from 350 to 860 nm. Time-resolved transient photoluminescence (PL) spectra were obtained on PL spectrometer, FLS 900, Edinburgh Instruments, excited with a picosecond pulsed diode laser (EPL-640) with the wavelength of 638.2 nm and measured at 775 nm after excitation. Fourier transform infrared spectra (FT-IR) were performed on TENSOR 27 spectrometer, Bruker. For FT-IR measurement, the samples were prepared as follows. Equal stoichiometric ratio of PbI2 and CPL was mixed and ground in a mortar till the sample turns uniformly dark brown. The same method is applied to afford perovskite-CPL adducts by grinding the mixture containing 1.35 mmol CPL, 1.15 mmol PbI2, 0.20 mmol PbBr2, 0.20 mmol MABr and 1.1 mmol FAI in the glove box until the color became dark brown. Constant temperature and humidity decay measurement were obtained under 70 \\u00b0C and relative humidity (RH) of 70% in a humidity chamber (KCL-1000) from EYELA. J-V characteristics were measured under AM 1.5 simulated sunlight (100 mW cm\\u22122), Zolix SS150A, which were recorded on a digital source meter (Keithley model 2602). The solar cells were masked with a black aperture to define the active area of 0.1 cm2, the scanning speed was 30 mv s\\u22121 with a delay time of 0.3 s. Incident photon-to-current conversion efficiency (IPCE) spectra were measured with a lab-made setup under 0.3\\u20130.9 mW cm\\u22122 monochromic light illumination without bias illumination . Transient photovoltage (TPV) spectra were obtained by our lab-made setup, in which the cell was excited by 532 nm pulse laser (Brio, 20 Hz, 4 ns) and the photovoltage decay process was recorded by a digital oscilloscope (Tektronix, DPO 7104).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.83MA0.17PbBr0.51I2.49,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 170; 100,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 30.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Polymer PN4N was synthesized according to our published reference. .\\nA general synthetic procedure of Au NPs doped PN4N was suitable for different weight ratio of Au NPs to PN4N. Taking a 10% weight ratio for example, 10\\u00a0uL HAuCl4 aqueous solution (10.5\\u00a0mg/mL) was added into 1\\u00a0mL of PN4N alcohol solution (0.5\\u00a0mg/mL) in a glass tube, and then the mixture was ultrasonicated for 20\\u00a0s. The mixture was immediately heated to reflux for 45\\u00a0min. During the reaction procedure, the color of the reaction mixture was turned to light red, and then to deep red. Finally the solution was cooled to room temperature and was directly used to spin-coat the cathode interfacial layer without any post-treatments. (Fig.\\u00a01(c)) Au NPs capped by sodium citrate were synthesized accordingly to the published reference. .\\n\\nThe polymer solar cells and perovskite solar cell are all fabricated in a glove box with oxygen and water content less than 1\\u00a0ppm. For the PSC device, a 40\\u00a0nm PEDOT:PSS (with or without Au NPs) layer was spin-coated on a ITO substrate, and the active layer (PCDTBT/PC71BM\\u00a0=\\u00a01:2 with a total concentration of 15\\u00a0mg\\u00a0mL\\u22121 in chlorobenzene) was then spin-coated (1200\\u00a0rpm) onto the PEDOT:PSS layer with resulted thickness of 80\\u00a0nm. The CIMs (with or without Au NPs) were spin-coated (2000\\u00a0rpm) onto active layer from methanol solution with a thickness of 5\\u00a0nm. Then the devices were transferred into a thermal evaporation chamber with a vacuum level of 3\\u00a0\\u00d7\\u00a010\\u22126\\u00a0mbar. Finally 80\\u00a0nm-thick Al was thermally deposited as cathode through a shadow mask (defined active area of 0.16\\u00a0cm2) in a chamber with a vacuum level of 3\\u00a0\\u00d7\\u00a010\\u22126\\u00a0mbar. For the PVKSC devices, the CH3NH3PbI3\\u2212xClx precursor solution (CH3NH3I:PbCl2\\u00a0=\\u00a03.5:1 in DMF) was spun cast (4000\\u00a0rpm) on the PEDOT:PSS (with or without Au NPs) layer resulted in a composite film with a thickness of \\u223c280\\u00a0nm. The films were then further annealed at 100\\u00a0\\u00b0C for 15\\u00a0min to promote crystallization of the CH3NH3PbI3\\u2212xClx perovskite. Then 50\\u00a0nm-thick PC61BM was spun (1400\\u00a0rpm) cast onto the CH3NH3PbI3\\u2212xClx layer. After that, The CIMs (with or without Au NPs) were deposited from isopropanol solution with the thickness of 5\\u00a0nm. Finally, 80\\u00a0nm-thick Al was thermally deposited as cathode to complete the device fabrication.\\n\\nCurrent density\\u2013voltage (J\\u2013V) characteristics were measured under an AM1.5G solar simulator (Model 91192, Oriel, USA). The light intensity was calibrated using a National Renewable Energy Laboratory (NREL) calibrated silicon photodiode with a KG5 filter. The photo and dark current density\\u2212voltage (J\\u2212V) characteristics were recorded with a Keithley 2410 and a Keithley 236 source meter, respectively. UV\\u2013visible absorption spectra were recorded on a HP 8453 UV\\u2013Vis spectrophotometer. Atomic force microscopy (AFM) measurements were carried out using a Digital Instrumental DI Multimode Nanoscope IIIa in taping mode. Transmission electron microscope (TEM) was carried out on a JEM-100CXII, and the Au NPs doped PN4N solution were dropped onto the copper grid and dried for measurement. External quantum efficiency (EQE) measurements were taken using a monochromator (Newport, Cornerstone 130) joined to the same xenon lamp and a lock-in amplifier (Stanford Research Systems, SR 830) coupled to a light chopper. All the J\\u2013V curves of perovskite solar cells in this study were measured under forward voltage bias.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PN4N,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite solution was prepared by dissolving PbI2 (1\\u00a0mmol, Sigma-Aldrich, 99%), FAI (0.85\\u00a0mmol, Dyesol), cesium iodide (0.15\\u00a0mmol, CsI, Sigma-Aldrich) and N,N-dimethyl sulfoxide (1\\u00a0mmol, DMSO, Sigma-Aldrich) in 1\\u00a0mL of N,N-Dimethylformamide (DMF, Sigma-Aldrich). Various amount of MACl (Sigma-Aldrich) was added in the precursor solution with a molar ratio of MACl/PbI2 in the range of 10%\\u201350%. Due to solubility limits of chloride ion and cesium ion in DMF, the solution cannot be fully dissolved with molar ratios higher than 50% . The solution was stirred overnight before use.\\n\\nThe devices have an inverted structure of ITO/PEDOT:PSS (40\\u00a0nm)/Cs0.15FA0.85PbI3 (250\\u00a0nm)/C60 (20\\u00a0nm)/BCP (8\\u00a0nm)/Ag (70\\u00a0nm). Patterned indium tin oxide (ITO) coated glass substrates (Lumtech) or polyethylene terephthalate (PET) substrates were used for rigid and flexible devices, respectively. The substrates were cleaned with Decon 90, rinsed with deionized water, and dried in an oven, followed by ultraviolet ozone treatment for 20\\u00a0min. Then, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, Baytron P-VP AI4083) was spin-coated onto the substrates at 3000\\u00a0rpm for 40\\u00a0s and annealed at 120\\u00a0\\u00b0C for 15\\u00a0min in ambient environment. Afterward, the samples were transferred into a N2-filled glovebox for deposition of perovskite layer. Perovskite solution was spin-coated at 3000\\u00a0rpm for 40\\u00a0s, in which 100\\u00a0\\u03bcL of toluene (Sigma-Aldrich) was dropped on the spinning substrates at 15\\u00a0s. After spin coating, the substrates were solvent annealed in DMF vapor at 120\\u00a0\\u00b0C for 10\\u00a0min . Finally, the devices were finished by thermal deposition of C60 (Lumtech), 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP, Lumtech) and an Ag electrode in sequence. The device area was 0.1\\u00a0cm2, as defined by the overlapping of the ITO and the Ag electrodes. The devices were encapsulated in a glovebox and characterized in air.\\n\\nSurface morphologies of samples were studied with scanning electron microscopy (SEM, Philips XL30 FEG SEM). Analysis of elemental composition was also conducted using the same SEM equipped with an energy-dispersive X-ray (EDX) analyzer. X-ray diffraction (XRD) measurements were recorded using a Philips X'Pert diffractometer at a step of 0.02\\u00b0. A PerkinElmer model Lambda 2S UV\\u2013vis spectrometer was used to measure the absorption spectra. Photoluminescence (PL) spectra were measured with a Cary Eclipse fluorescence spectrometer. External quantum efficiencies (EQEs) of the devices were determined by an EQE system (model Oriel IQE 200). Current density-voltage (J-V) curves were measured with a Keithley 236 source meter under one sun illumination (100\\u00a0mW\\u00a0cm\\u22122) from an Oriel 150\\u00a0W solar simulator with AM1.5G (AM, air mass; G, global) filters.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: Cs0.15FA0.85PbI3,\\n Perovskite_composition_short_form: CsFAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite (CH3NH3PbI3-xClx) films were prepared using a hot-casting technique. Perovskite (CH3NH3PbI3-xClx) solution was prepared by dissolving equimolar ratios of lead iodide (PbI2, Sigma-Aldrich, 99%) and methylamine hydrochloride (MACl, Sigma-Aldrich) in N, N-dimethylformamide (DMF, Sigma-Aldrich, anhydrous, 99.8%) in 11\\u00a0wt% concentration. The perovskite solutions were ready for use after heating in a hot plate at different temperatures of 40, 70 and 90\\u00a0\\u00b0C for 24\\u00a0h with magnetic stirring in a N2 filled glove box. FTO/glass substrates were cleaned with four times sonication (each for 10\\u00a0min) in de-ionized (DI) water, methanol, acetone, and 2-propanol (IPA), respectively. Afterwards, the substrates were dried with nitrogen, followed by heating in a hot plate at 120\\u00a0\\u00b0C for 15\\u00a0min to remove the last traces of any solvent. For optical characterization, perovskite solutions heated at different solution temperatures of 40, 70 and 90\\u00a0\\u00b0C were spin-coated on glass slides preheated at 180\\u00a0\\u00b0C. For perovskite solar cells, PEDOT:PSS diluted by using 2-propanol in a ratio of 1:3 was spin coated on FTO/glass substrates at a speed of 3000\\u00a0rpm. In addition, perovskite thin films were prepared on preheated PEDOT:PSS/FTO/glass at 180\\u00a0\\u00b0C with perovskite solutions heated at different solution temperatures of 40, 70 and 90\\u00a0\\u00b0C. The electron transport layer consists of PCBM(Nano-c) dissolved in di-chlorobenzene (Sigma-Aldrich) that was spin coated on the top of perovskite layer at a speed of 1500\\u00a0rpm in a N2 containing glove box. Silver was deposited by using electron beam evaporation. Therefore, the resultant perovskite solar cells consisted of FTO/PEDOT:PSS/MAPbI3-xClx/PCBM/Ag. Scanning electron microscope (SEM) results showed that the thickness of the perovskite layer depended on the perovskite solution temperature and was 210\\u00a0\\u00b1\\u00a08\\u00a0nm, 252\\u00a0\\u00b1\\u00a07\\u00a0nm and 270\\u00a0\\u00b1\\u00a06\\u00a0nm\\u00a0at perovskite solution temperatures of 40, 70 and 90\\u00b0 C. In addition, the thickness of PEDOT:PSS and PCBM layers was measured to be about tens of nanometers and Ag metal was measured to be about 180\\u00a0nm.\\n\\nSteady-state and time-resolved photoluminescence (PL) measurements were performed using Horiba FluoroLog-3 spectrofluorometer and time-correlated single photon counting (TCSPC) with a solid-state laser with 450\\u00a0nm, which was used for the various excitation intensities. Both a continuous 450\\u00a0W xenon lamp and pulsed laser-diode were used to measure steady-state PL and lifetime decays. Particularly, the TCSPC is fiber-coupled into Olympus BX53F microscope equipped with a CCD camera capable of measuring PL and lifetime mappings while showing microscopic morphologies. To record photoluminescence (PL), perovskite samples were coated with PMMA to prevent degradation from air environment. The UV-VIS spectra were measured by using Perkin Elmer Lambda 45 spectrophotometer. To measure UV-VIS, active layer of perovskite was prepared on top of a glass substrate. The current-voltage (I-V) characteristics were recorded in ambient air by using Keithley 2400 under AM1.5 condition (100\\u00a0mW/cm2) of a solar simulator (Newport 69907).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: E-beam evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite (CH3NH3PbI3-xClx) films were prepared by dissolving equimolar ratios of lead iodide (PbI2, Sigma-Aldrich, 99%) and methylamine hydrochloride (MACl, Sigma-Aldrich) in N, N-dimethylformamide (DMF, Sigma-Aldrich, anhydrous, 99.8%) in 11\\u202fwt% concentration. In this case, 0.09\\u202fg PbI2 and 0.013\\u202fg MACl were mixed in 1\\u202fml DMF and stirred well at 70\\u202f\\u00b0C for 24\\u202fh. For perovskite solar cells, FTO/glass substrates were cleaned with de-ionized (DI) water, methanol, acetone, and 2-propanol (IPA), respectively. Subsequently, the substrates were dried with nitrogen and then heated on a hot plate at 120\\u202f\\u00b0C for 15\\u202fmin to remove the last traces of any solvent. PEDOT:PSS diluted with 2-propanol in a ratio of 1:3 was spin-coated onto the FTO/glass substrates at a speed of 3000\\u202frpm. And then, perovskite thin films were formed by a hot-casting technique at 180\\u202f\\u00b0C using perovskite solution heated at a solution temperature of 70\\u202f\\u00b0C. PCBM(Nano-c) dissolved in di-chlorobenzene(Sigma-Aldrich) was spin-coated on top of perovskite layer at a speed of 1500\\u202frpm in a N2 containing glove box at room temperature. C60 and silver were deposited by using electron beam evaporation []. The resultant perovskite solar cells consisted of FTO/PEDOT:PSS/MAPbI3-xClx/PCBM or PCBM/C60/Ag. The thickness was measured by a cross-section secondary electron microscope (SEM) and the measured thickness of the MAPbI3-xClx layer was about 252\\u202fnm []. The PEDOT:PSS, PCBM, and C60 layers were also measured to be about tens of nanometers and the thickness of Ag metal was about 180\\u202fnm. The current-voltage (J-V) characteristics were recorded in ambient air by using Keithley 2400 under AM1.5 condition (100\\u202fmW/cm2) of a solar simulator (Newport 69907). Steady-state and time-resolved photoluminescence (PL) measurements were performed using Horiba FluoroLog-3 spectrofluorometer and a time-correlated single photon counting (TCSPC) with a solid-state laser with 450\\u202fnm. To record PL, perovskite samples were coated with PMMA to prevent degradation from air environment.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | C60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Hot-casting,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: E-beam evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"N,N-dimethylformamide (DMF) was purchased from Sigma-Aldrich. Isopropanol and chloroform were obtained from Beijing Chemical Factory, China. Methylammonium iodide (MAI) and lead chloride (PbCl2) were purchased from Yingkou Optimal Choice Trade, China. [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) was purchased from American Dye Source. The bis-functionalization of C70 (Bis-C70) was purchased from 1-Material, Canada. \\u03b1, \\u03c9-diamino poly (ethylene glycol) (PEG-NH2) (molecular weight, Mw\\u202f=\\u202f10\\u202f000; polydispersity index, PDI\\u202f=\\u202f1.3) was synthesized in our laboratory. All materials were used as received.\\n\\nThe solar cells were fabricated on ITO-coated glass substrates. The ITO-coated glass substrates were first cleaned with detergent, then ultrasonicated in deionized water, acetone, and isopropanol, respectively, then dried by nitrogen flow. After treating the ITO substrate with UV ozone for 25\\u202fmin, a 30\\u202fnm thick poly- (ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, Baytron P4083) layer was spin-coated on this well-cleaned ITO glass and dried at 140\\u202f\\u00b0C for 30\\u202fmin. The substrates were transferred into a N2-filled glovebox. Then the solution containing a mixture of MAI:PbCl2 (MAI: PbCl2 with a molar ratio of 3:1 in DMF and the total concentration is 30\\u202fwt%) with different content of PEG-NH2 was spin-cast on top of the PEDOT:PSS layer to produce a 300\\u202fnm thick active layer and annealed at 80\\u202f\\u00b0C for 5\\u202fh. Afterward, the PC61BM (15\\u202fmg/mL in chloroform) and C70-bis surfactant (1\\u202fmg/mL in isopropanol) were sequentially deposited on the active layer by spin coating at 3000\\u202frpm for 60\\u202fs, respectively. Finally, a layer structure of Al (100\\u202fnm) was deposited at top of the active layer by thermal evaporation in a vacuum of 2\\u202f\\u00d7\\u202f10\\u22124\\u202fPa to complete the device fabrication.\\n\\nThe morphology images of the perovskite films were investigated by field-emission scanning electron microscopy (FESEM) using a Micro FEI Philips XL-30-ESEMFEG microscope. The samples were sputter coated with gold before FESEM observation.\\nThe crystallinity of the perovskite films were analyzed using out-of-plane grazing incidence X-ray diffraction (GIXD) measurements and two-dimensional GIXD (2D GIXD). The GIXD profiles were obtained by using a Bruker D8 Discover Reflector with an X-ray generation power of 40\\u202fkV tube voltages and 40\\u202fmA tube current. 2D GIXD images were recorded by using a Rigaku SmartLab instrument (with an X-ray generation power of 40\\u202fkV tube voltage and 30\\u202fmA tube current). Grazing Incidence Wide-Angle X-ray Scattering (GIWAXS) scattering patterns were collected at BL1W1A at Beijing Synchrotron Radiation Facility (BSRF; l\\u202f=\\u202f1.54\\u202f\\u00c5).\\nTo illustrate the crystallization process, time dependent UV\\u2013vis absorption spectra (In-stiu UV\\u2013vis absorption spectra) was performed by combining UV\\u2013vis absorption spectroscopy (AvaLight-Hal with halogen lamp source) with a home-made heater. The perovskite films were annealed at 80\\u202f\\u00b0C under nitrogen atmosphere. In situ two-dimensional detection capability (2D-GIXD) was performed by combining Rigaku SmartLab instrument (with an X-ray generation power of 40\\u202fkV tube voltage and 30\\u202fmA tube current) with a home-made heater. The perovskite film was annealing at 80\\u202f\\u00b0C under vacuum.\\nNanosecond fluorescence lifetime experiments were performed using the time-correlated single-photon counting (TCSPC) system under right-angle sample geometry. A 400\\u202fnm\\u202fpicosecond diode laser (Edinburgh Instruments EPL375, repetition rate 20\\u202fMHz) was used to excite the samples. The fluorescence was collected by a photomultiplier tube (Hamamatsu H5783p) connected to a TCSPC board (Becker & Hickl SPC-130). The time constant of the instrument response function (IRF) is about 220\\u202fps?\\nCurrent density\\u2013voltage (I\\u2013V) characteristics of the solar cells were measured using a computer controlled Keithley 236 source meter under AM1.5G illumination from a calibrated solar simulator with an irradiation intensity of 100\\u202fmW\\u202fcm\\u22122. An aperture size of 10.6\\u202fmm2 was used to define the light absorption area, which would avoid the overestimation of the photocurrent density by the optical pining effect [].\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C70,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Cl,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80,\\n Perovskite_deposition_thermal_annealing_time: 300,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.106,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fullerene C60 (99.9%) was purchased from Dade Carbon Nanotechnology Co., Ltd, H2O2 (30\\u202fwt%) was bought from Aladdin Industrial Corporation, NaOH (AR) and methanol were purchased from Sinopharm Chemical Reagent Co., Ltd and Chinasun Specialty Products Co., Ltd, respectively. And all these samples are used without further purification.\\nWe synthesized Methylammonium iodide (MAI) in our laboratory according to the literature []. PbI2 (99.999%) was bought from Alfa Aesar, Methylammonium Chloride (MACl) was purchased from Xi'an Polymer Light Technology Crop. P3HT was obtained from Rieke Metals, lnc.\\n\\nITO substrates were sequentially cleaned 20\\u202fmin by ultrasonic in detergent, deionized water, acetone, ethanol and isopropyl alcohol. After being dried at 150\\u202f\\u00b0C for 10\\u202fmin, the ITO glass was treated for 20\\u202fmin with ultraviolet ozone (UVO) to increase affinity for water molecules. The C60(OH)16 was dissolved in deionized water at four different concentrations of 0.3\\u202fmg/mL, 0.5\\u202fmg/mL 0.7\\u202fmg/mL and 1\\u202fmg/mL. And then these solutions were spin-coated on ITO substrates at 1500\\u202frpm for 50s. The substrates were transferred into the glove box with nitrogen atmosphere after annealed at 120\\u202f\\u00b0C for 20\\u202fmin. 12\\u202fnm of C60 was deposited on top of the C60(OH)16 fullerenol using the method of vacuum evaporation.\\n461\\u202fmg PbI2 was dissolved in 1\\u202fmL\\u202fN, N-dimethylformamide (DMF, 99.8%, J&K), 50\\u202fmg MAI and 5\\u202fmg MACl (mass ratio of 10:1) were dissolved in 1\\u202fmL isopropanol (IPA, J&K). All the precursor solutions were placed on a hot plate at 70\\u202f\\u00b0C and stirred for 12\\u202fh. These precursor solutions were filtered by 0.45\\u202f\\u03bcm polytetrafluoroethylene (PTFE) filter before use. The perovskite active layer was deposited using the method of sequential two-step deposition. 40\\u202f\\u03bcL of PbI2 solution was spin-coated on the top of C60 at 4500\\u202frpm for 45\\u202fs. During this process, additional 40\\u202f\\u03bcL of the mixed solution of MAI: MACl (10:1) was further dropped on the spinning substrate 25\\u202fs prior to the end of this PbI2 coating procedure. Thermal annealing for the film was processed at 100\\u202f\\u00b0C for 3\\u202fmin in a nitrogen atmosphere. Perovskite films turned dark immediately after annealing.\\n30\\u202fmg\\u202fP3HT as a hole transport material was dissolved in 1\\u202fmL o-dichlorobenzene, which added with 20.4\\u202f\\u03bcL bis(trifluoromethane) sulfonamide lithium salt (Li-TFSI) solution (28.3\\u202fmg Li-TFSI in 1\\u202fmL acetonitrile) and 10.2\\u202f\\u03bcL 4-tertbutylpyridine (t-BP). P3HT HTL was spin-coated on the top of perovskite at 1500\\u202frpm for 60\\u202fs. 7\\u202fnm of MoO3 was deposited by vacuum evaporation as buffer layer. Finally, 80\\u202fnm of Ag was vacuum evaporated as a counter electrode using a mask plate. 0.0757\\u202fcm2 of measuring active area was defined by a shadow mask. The configuration of ITO/C60(OH)16/C60/Au was used to measure the direct current conductivity. 80\\u202fnm Au was vacuum evaporated and using a shadow mask with an active area of 0.064\\u202fcm2.\\n\\nThe instrument of Bruker VERTEX 70\\u202fV (Germany) was used to obtain Fourier transform infrared spectrometer (FTIR) spectra. Thermal gravimetric analysis (TGA) was obtained with a PerkinElmer Pyris 6. Work function (WF) was measured by Ultraviolet photoelectron spectroscopy (UPS, Escalab 250Xi, Thermo Fisher, USA). Current density\\u2212voltage (J\\u2212V) curves of a perovskite solar cells (Pero-SCs) were acquired by applying an external voltage bias and using Keithley 2400 digital source meter to record the current response. A Xenon arc lamp with power of 100\\u202fmW/cm2 simulated Air Mass 1.5 global (AM 1.5G) solar illumination. Steady-state photocurrents under applied voltage were obtained in the same instrument. The measurements of J-V and steady-state photocurrents were carried out in glove box. Incident photo-to-current conversion efficiency (IPCE) of Pero-SCs was measured using Enli Technology Co., Ltd. QE-R3011 in air without bias light. Standard commercial single-crystal silicon solar cells were used to corrected illumination intensities. Using spectroscopic ellipsometer (M-2000 V, J. A. Woollam Co., USA) measure the thicknesses of fullerenol films. SU8010 (Hitachi produced) was used to acquire scanning electron microscopy (SEM) images. X-ray diffraction (XRD) patterns (2\\u03b8 scans) were recorded by X-ray diffractometer (D2 PHASER, Bruker, Germany) from 10\\u00b0 to 70\\u00b0 with radiation source angle \\u03bb\\u202f=\\u202f1.54184\\u202f\\u00c5. Ultraviolet-visible (UV-vis) spectra were carried out using an UV-vis spectrophotometer (Cary 6000, Agilent). Steady-state photo-luminescence (PL) were measured on FLS980 (Edinburgh Instrument, UK) with excitation wavelength is 470\\u202fnm. Time-resolved PL spectra were acquired on Lifespec (Edinburgh Instrument, UK) with a 477\\u202fnm laser (5\\u202fMHz). The alternating current impedance spectrometry (ACIS) was obtained in dark condition using IM6 electrochemical workstation (Zahner Zennium, Germany). The bias voltage is 1.0\\u202fV and the frequency ranged from 0.1\\u202fHz to 4\\u202fMHz. The effective area of the cell is 0.1842\\u202fcm2. The impedance spectra was fitted by Z-view software to obtain the impedance parameters.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 3.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0757,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Materials: PbI2 (99.99%), CH3NH3I (\\u226599.5%), 4-tertbutylpyridine (tBP, 96%) lithium bis-(trifluoromethanesulfonyl) imide (Li-TFSI, 99.9%), 2,2\\u2032,7,7\\u2032-Tetrakis (N,N\\u2032-di-pmethoxyphenylamine)-9,9\\u2032-spirobifluorene(spiro-OMeTAD, 99.5%), were purchased from Xi'an Polymer Light Technology Corporation. Acetonitrile (99.9%) N, N-dimethylformamide (DMF, 99.9%), and chlorobenzene (99.9%) were achieved from Sigma-Aldrich. The SnO2 colloid precursor purchased from Alfa Aesar (tin (IV) oxide, 15% in H2O colloidal dispersion). Pyrene (97%) obtained from Aladdin. All the materials used without any further purification.\\nSynthesis of GQDs: GQDs were synthesized use an alkali-mediated hydrothermal methods [,]. Firstly, 1.5\\u202fg 1, 3, 6-trinitropyrene was dispersed in 300\\u202fml deionized water solution containing 0.4\\u202fM NaOH under ultrasonication for 2.5\\u202fh to acquire a homogeneous suspension, then transferred to 250\\u202fml Teflon-lined stainless-steel autoclave and heated at 200\\u202f\\u00b0C for 10\\u202fh in drying oven. Secondly, the GQDs solution was filtered with a 0.22\\u202f\\u03bcm microporous membrane to removal of insoluble carbon produce, and then purified in a dialysis bag (retained molecular weight: 3500\\u202fDa) for 3 days, aiming to separate indissoluble small molecules and sodium salt. Finally, the GQD powders were obtained through rotary evaporation and drying at a temperature of 80\\u202f\\u00b0C in oven.\\nDevice Fabrication: The FTO coated glass substrates were sequentially ultrasonic cleaned with detergent, acetone, deionized water, ethanol for 15\\u202fmin, respectively. A 15\\u202fmin ultraviolet-ozone treatment carried out to remove the residual organics and improve the work function of FTO substrates. The SnO2 aqueous solution was diluted with deionized water (volume rate 1:6) before using, and then was deposited by spin-coating at 3000\\u202frpm for 30\\u202fs as the electron transport layers on FTO substrates, and the SnO2 aqueous solution was filtered through a 0.22\\u202f\\u03bcm filter before using. The SnO2 layer annealed at 150\\u202f\\u00b0C for 30\\u202fmin on a hotplate. 2\\u202fmg GQDs powder dissolved in 40\\u202fml deionized water to obtained 0.05\\u202fmg/ml GQDs aqueous solution. The GQDs deposited on SnO2 layer by UAP, and heated at 100\\u202f\\u00b0C for 10\\u202fmin to evaporate moisture. The solution infuse rate is 0.35\\u202fml/min, the working pressure is 1.5 psi, and controlled deposition variable by change working time. The UAP intelligently controlled by computer programs, no need manual operation. The advantages of UAP are high solution utilization rate, high automation, micron level atomization ability, scale-up manufacturing and open-air operation. Then the perovskite layer was deposited by one-step spin coating method in a glove-box. The 553.2\\u202fmg of PbI2, 190.8\\u202fmg of CH3NH3I (molar rate 1:1) were mixed in 1\\u202fmol of DMF solution. The precursor solution filtered through a 0.22\\u202f\\u03bcm filter before using. The prepared precursor solution was dropped on the FTO/SnO2 or FTO/SnO2/GQDs substrates, and quickly spin-coated at 3000\\u202frpm for 55\\u202fs. 80\\u202f\\u03bcl chlorobenzene was drop casted quickly at 10\\u202fs before the 3000\\u202frpm spin-coating ended. Then the substrates heated at 100\\u202f\\u00b0C for 20\\u202fmin on a hot plate. After the perovskite films were naturally cooled to room temperature, a hole-transport material was spin coated on the top of perovskite film at 3000\\u202frpm for 30\\u202fs in a glove-box. The hole-transport materials solution containing Spiro-OMeTAD (72.3\\u202fmg), 4-tert-butylpyridine (tBP, 28.8\\u202f\\u03bcL), Li-TFSI/acetonitrile solution (17.5\\u202f\\u03bcL, 520\\u202fmg/ml) and chlorobenzene (17.5\\u202f\\u03bcL). Finally, Au back electrode deposited by magnetron sputtering at a pressure of 4.0\\u202f\\u00d7\\u202f10\\u22123\\u202fPa. The active area of device controlled to 0.16\\u202fcm2.\\nMeasurement and characterization: The AFM image scanned by an atomic force microscope (AFM, Agilent 7500). The SEM image were scanned by a scanning electron microscopy (SEM, ZEISS EV0MA15), and the EDX maps obtained from energy dispersive X-ray spectroscopy (EDX) detector. The crystal structure of the perovskite films was characterized by X-ray diffraction (XRD; DX-2700, Dandong) with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f0.15406\\u202fnm) at a scanning rate of 5 deg/min. The absorption spectra of the films were measured using a ultraviolet\\u2013visible spectrophotometer (UV-2600, SHIMADZU). The steady and time-resolved photoluminescence (TRPL) spectroscopy measured at 760\\u202fnm with the 510\\u202fnm excitation at a pulse frequency of 1\\u202fMHz (FLS980, Edinburgh). The J-V characteristic of device was recorded using an electrochemical workstation under a simulated solar spectrum (AM1.5) provided by a solar simulator (Zolix SS150, Beijing, China). Electrochemical impedance spectroscopy (EIS) measured using CHI660D electrochemical analyzer (Chenhua, China). The monochromatic incident photon-to-current efficiency (IPCE) measured using an IPCE system (PVE300, Bentham, Inc.) from 300 to 800\\u202fnm.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-np | Graphene-QDs,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Ultrasonic spray,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Magnetron sputtering,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Imidazole (>99.0%) and benzimidazole (>98.0%) were purchased from Sinopharm Chemical Reagent Co., Ltd. PTAA was obtained from Xi'an Polymer Light Technology Corp. Methylammonium iodide (MAI, 99.5%) was purchased from Shanghai Mater Win New Materials Co., Ltd. PbCl2 (99.999%), PbI2 (99.999%), pyridine and bathocuproine (BCP) were purchased from Sigma-Aldrich. Anhydrous dimethylformamide (99.9%), and chlorobenzene (99.9%) were purchased from Alfa Aesar. PC61BM was manufactured by Solarmer Materials Inc. All materials were used as received without further purification.\\n\\n1H NMR spectra were recorded on a Bruker AV400 spectrometer. Dimethyl sulfoxide-d6 was used as solvent and internal standard. Raman spectra were recorded on a Horiba instrument (HR Evolution, 514 and 633\\u00a0nm excitation laser). The UV\\u2013vis absorption spectra were recorded on a Shimadzu UV2600 spectrophotometer. Steady-state photoluminescence (PL) spectra were obtained using a Horiba Fluoromax-4 instrument with an excitation wavelength of 475\\u00a0nm. The time-resolved PL (TRPL) spectra were measured with Lifespec II (Edinburgh Instrument, U.K.) with picosecond light pulser (Hamamatsu) using a pump light wavelength of 477\\u00a0nm and probe wavelength of 776\\u00a0nm. X-ray photoelectron spectroscopy (XPS) analysis was performed on an ESCALAB 250 spectrometer equipped with an Al K\\u03b1 excitation source with photon energy of 1486.6\\u00a0eV. Atomic force microscopy (AFM) height images were obtained in tapping mode on an MFP-3D-BIO (Asylum Research) instrument. Scanning electron microscopy (SEM) characterizations were performed with a Hitachi SU8010 instrument. The ESR spectra were obtained at room temperature under nitrogen atmosphere using a JEOL JES-X320 instrument. PC61BM solution (10\\u00a0mg in 500\\u00a0\\u03bcL chlorobenzene) with 160\\u00a0\\u03bcL pyridine solution containing 1.6\\u00a0mg BIZ was added to an ESR test tube and then degassed with nitrogen to form films on the tube walls. The electrical conductivities of the PC61BM thin films were measured by using a four point probe setup with a source measurement unit (Keithley 4200).\\n\\nThe inverted planar PeSCs were fabricated utilizing previously reported methods [,]. Briefly, ITO-coated glass sheets were subsequently washed with deionized water, acetone, isopropanol and finally treated with UVO for 15\\u00a0min. A PTAA HTL was prepared by spin-coating the PTAA toluene solution (2\\u00a0mg\\u00a0mL\\u22121) onto ITO at 5000\\u00a0rpm for 40\\u00a0s and dried at 100\\u00a0\\u00b0C for 10\\u00a0min. The MAPbI3-xClx PVK layer was prepared by a simple one-step spin-coating method without antisolvent treatment. The PVK precursor solution composed of 1.2\\u00a0M MAI, 0.36\\u00a0M PbI2 and 0.22\\u00a0M PbCl2 was spin-coated onto the substrate at 4000\\u00a0rpm for 40\\u00a0s under N2 atmosphere, followed by a thermal annealing at 80\\u00a0\\u00b0C for 2\\u00a0h. For the deposition of ETL, 20\\u00a0\\u03bcL chlorobenzene solution of PC61BM (20\\u00a0mg\\u00a0mL\\u22121) was spin-coated onto the PVK layer at 2000\\u00a0rpm for 30\\u00a0s. For preparing doped PC61BM layer, IZ or BIZ additive was dissolved in a pyridine solution with a concentration of 10\\u00a0mg\\u00a0mL\\u22121 and 1\\u201325\\u00a0\\u03bcL such solution was added into the PC61BM solution (500\\u00a0\\u03bcL) before spin-coating. The doping ratio of IZ or BIZ is optimized by varying the amount of their pyridine solution (see Fig. S1). Then, an ethanol solution of BCP (1.5\\u00a0mg\\u00a0mL\\u22121) was spin-coated on the ETL layer. Finally, Ag electrodes (ca. 100\\u00a0nm thick) were deposited under high vacuum (<1.0\\u00a0\\u00d7\\u00a010\\u22125\\u00a0Pa) through a shadow mask to define the effective active area of the device (0.04\\u00a0cm2). The electron-only device was fabricated with a structure of ITO/PC61BM/perovskite/ETL/BCP/Ag.\\nThe device stability was measured for the PeSCs stored under N2 atomosphere. Alternatively, white light-emitting diode (WLED; 40\\u00a0W) was continuously illuminated onto the PeSCs at open-circuit conditions with a diatance of 20\\u00a0cm under N2 atomosphere. The time-dependant PCE and related parameters were measured under standard contionds.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: IZ | Undoped,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: Undoped,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 80,\\n Perovskite_deposition_thermal_annealing_time: 120,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless stated otherwise, all chemicals were purchased from the Sigma-Aldrich or Alfa Aesar Crop and used as received. Methylammonium iodide (MAI), formamidinium iodide (FAI) were purchased from Xi'an Polymer Light Technology Crop, China. Hole transport material (Spiro-OMeTAD) was purchased from Luminescence Technology Crop, Taiwan, China.\\n\\nFTO glass (Pilkington, TEC-8, 8 \\u03a9 sq\\u22121) was cleaned sequentially with ethanol, acetone and isopropanol in an ultrasonic bath for 30 min, and treated in a UV-ozone (UVO) cleaner for 20 min. The compact TiO2 blocking layer (c-TiO2) about 50 nm was spin-coated on the FTO glass at 3000 rpm for 20 s using 0.2 M titanium diisopropoxide bis(acetylacetonate) (75 wt% in isopropanol, Aldrich) in 1-butanol (99.8%, Aldrich) solution, and then was heated at 550 \\u00b0C for 30 min. A planar heterojunction photovoltaic device with the structure Au (\\u223c80 nm)/Spiro-OMeTAD (\\u223c200 nm)/perovskite (\\u223c400 nm)/TiO2 (\\u223c50 nm)/FTO (\\u223c500 nm) was fabricated by spin-coating method and the schematic diagram is shown in Fig. 1 . The FAPbI3 precursor solution with concentrations of 0.65, 0.85, 1.05, 1.25 and 1.45 M were prepared by dissolving PbI2 and FAI with the molar ratio of 1:1 in a mixed solvent of N,N-dimethylformamide (DMF, 99.8%, Aldrich) and dimethyl sulfoxide (DMSO, 99.8%, Aldrich) with the volume ratio of DMF/DMSO at 4:1 (Xing et al., 2013). The FAPbI3 precursor solution was spin-coated on the TiO2 compact layer at 1000 rpm for 5 s with an acceleration of 1000 rpm and 5000 rpm for 20 s with an acceleration of 2000 rpm. Then the 20 \\u00b5L of 1.05 M MAPbI3 solution consisting of PbI2 and MAI dissolved in a mixed solvent of DMF and DMSO was spin-coated on the intermediate phase FAPbI3 film at 4000 rpm for 30 s with continual dripping 0.5 mL of diethyl ether on the rotating substrate (Wehrenfennig et al., 2014), the molar ratio of PbI2, MAI and DMSO was 1:1:2.5. The resultant film was annealed at 100 \\u00b0C for 5 min to remove residual solvent and form a smooth, highly crystalline and dense MA1\\u2212xFxPbI3 perovskite film.\\n20 \\u00b5L of 2,2\\u2032,7,7\\u2032-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (spiro-OMeTAD) solution was spin-coated onto the perovskite layer at 800 rpm for 6 s and subsequently 4800 rpm for 20 s. A spiro-OMeTAD solution was prepared by dissolving 144.6 mg of spiro-OMeTAD in 2 mL of chlorobenzene, to which 57.6 \\u00b5L of 4-tert-butyl pyridine and 35 \\u00b5L of lithium bis(trifluoro-methanesulfonyl) imide (Li-TFSI) solution (520 mg LI-TSFI in 1 mL acetonitrile, Sigma-Aldrich, 99.8%) were added. All devices were stored in a desiccator (humidity < 20%) in the dark for 12 h. Finally, gold with thickness of 80 nm was coated on the spiro-OMeTAD by thermally evaporating under vacuum using a shadow mask.\\n\\nAbsorption spectra were measured by a UV\\u2013vis spectrophotometer (PerkinElmer Lambda 950) in the wavelength range of 300 to 800 nm. The crystallinities of perovskite films were examined by an X-ray diffractometer (XRD, Rigaku Smar/SmartLa), with a Cu K\\u03b1 radiation source and with the operation conditions of 40 kV and 30 mA. Fourier Transform infrared (FTIR) spectra were measured by a Thermo Scientific Nicolet 6700 FT-IR spectrometer. The perovskite films were observed using field-emission scanning electron microscopy (SEM, Hitachi S-4800, Japan). Time-resolved photoluminescence decay (TRPL) spectra were measured by exciting samples using a supercontinuum fiber laser at a wavelength of 500 nm, repetition rate of 0.1 MHz and 5 \\u03bcW laser power with the spot size being focused down to 300 \\u00d7 300 \\u03bcm2. Maximum emission was collected at a wavelength of 775 nm on a single-photon counter. IPCE curves were measured as a function of wavelength from 300 to 800 nm using the Newport IPCE system (Newport, USA). The current density-voltage (J-V) curves were obtained by a Keithley Model 2401 source-measure unit under AM 1.5 G illumination at 1000 W\\u22c5m\\u20132 using an Oriel Sol 3 A solar simulator with pre sweep delay of 0.04 s, max reverse bias of \\u22120.1 V, max forward bias of 2.0 V, num sweep points of 100, dwell time of 30 ms in ambient environment. The light intensity was calibrated using a NREL-standard Si solar cell equipped with a\\u00a0KG-2 filter. During the measurement, the photovoltaic devices were masked with a black metal aperture confining the active area to 0.136\\u00a0cm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.136,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals used are of analytical grade (AR) quality and without further purification. N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), lithium bistrifluoromethanesulfonimide, chlorobenzene, acetonitrile and 4-tert-butylpyridine were purchased from Sigma-Aldrich. PbI2, CsI and PbBr2 were purchased from Tokyo Chemical Industry (Shanghai) Development Corp., China. The formazan iodide (FAI) and cesium iodide (CsI), methyl ammonium bromide (MABr) salts were purchased from Xi'an Polymer Light Technology Corp., China. The hole transport material (Spiro-OMeTAD) was purchased from Luminescence Technology Corp., Taiwan, China. FTO with a surface resistance of 7\\u202f\\u03a9 was purchased from Wuhan Crystal Solar Technology Corp., China. All chemicals have not been further processed. The purity of the gold used for thermal evaporation was 99.999%.\\n\\nThe devices were fabricated on clean fluorine doped tin oxide (FTO) glass (7\\u202f\\u03a9\\u202fsq\\u22121) substrates with an area of 1.5\\u202f\\u00d7\\u202f1.5\\u202fcm2. The active area for devices were about 0.11\\u202fcm2. Before being used, the FTO glass was surface of the glass was cleaned with detergent, deionized water, and ethanol under ultrasonication for 30\\u202fmin, respectively for 30\\u202fmin. Finally, the glasses were treated with a plasma cleaner for 5\\u202fmin.\\nThe electron transport layer TiO2 film (150\\u202f\\u03bcL of titanium diisopropoxide bis(acetylacetonate) dissolved in 2\\u202fmL of butanol with stirring for 12\\u202fh) was spin-coated onto the treated FTO by rotation speed of 700\\u202frpm for 5\\u202fs and followed by 4000\\u202frpm for 20\\u202fs. Finally, the glass coated with TiO2 film was dried at 100\\u202f\\u00b0C for 10\\u202fmin and sintered at 550\\u202f\\u00b0C for 30\\u202fmin\\nA uniform perovskite film was obtained using a two-step spin-coating procedure. The precursor solution of FAI, CSI, MABr, PbI2 and PbBr2 were dissolved in a mixture of N, N-dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) (4:1 (v: v)) with stirring for 2\\u202fh, according to the stoichiometric ratio of Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3. The spin coating procedures was carried out in the Ar glove box by a consecutive two-step spin coating process, at first step was 1000\\u202frpm for 10\\u202fs followed by the and second step 6000\\u202frpm for 20\\u202fs. During the secondary coating step, chlorobenzene (100\\u202f\\u03bcL) as an anti-solvent was slowly dropped on the spinning substrate with 10\\u202fs prior to the end of the procedures. Then, the device was annealed at 100\\u202f\\u00b0C for 10\\u202fmin to volatilize the solvent on the surface. Finally, the device was further heated in a glass vessel containing mixed solvents of DMSO/CB (v: v) (1:10, 1:20, 1:30, 1:40, and 1:50) at 100\\u202f\\u00b0C for 40\\u202fmin. For comparison, the traditional device was prepared by annealing at 100\\u202f\\u00b0C for 50\\u202fmin. The annealing process were also carried out in the nitrogen filled glove box. In order to describe the sample more simply, the sample annealed with mixed solvent were denoted as B (1:10), C (1:20), D (1:30), E (1:40), F (1:50). For comparison, the sample annealed without mixed solvent was denoted as A.\\nThe spiro-OMeTAD solution was spin-coated onto the substrate with perovskite layer at 700\\u202frpm for 5\\u202fs followed by the and secondary coating 4000\\u202frpm for 20\\u202fs in the glove box. A spiro-OMeTAD solution was prepared by dissolving 72.3\\u202fmg of spiro-OMeTAD in 1\\u202fmL of chlorobenzene, and 28.8\\u202f\\u03bcL of 4-tert-Butylpyridine and 17.5\\u202f\\u03bcL of Li-TFSI solution (520\\u202fmg of bis (trifluoromethylsulfonyl) imide lithium salt in 1\\u202fmL of acetonitrile) were added into the solution with stirring at room temperature for 1\\u202fh. The substrate was oxidized in air with a humidity of 10% for 12\\u202fh. Finally, Au electrode of about 80\\u202fnm was vapor-deposited using a thermal evaporation method under high vacuum.\\n\\nThe cross-sectional SEM images of PSC devices and the morphologies of perovskite films were obtained using a Hitachi SU800 FE-SEM instrument. The crystalline structures of the perovskites were measured using X-ray diffraction (XRD, Bruker D8 Advance X-ray diffractometer). Keithley's 2400 light source was used to record the J-V photovoltaic performance of a perovskite solar cell under 100\\u202fmW\\u202fcm\\u22122 1 sun AM 1.5G simulated spectrum. The delay time is 10\\u202fms. The forward scan started from \\u22120.1\\u202fV to 2.0\\u202fV, and the reverse scan started from 2.0\\u202fV to \\u22120.1\\u202fV. NREL-calibrated silicon solar cells were used to match the light intensity equipped with KG-2 filters. Lamda 950 UV\\u2013Vis\\u2013NIR spectrophotometer was used to measure the absorption of visible light by perovskite solar cells. Steady-state photoluminescence (PL) spectra were measured using a fluorescence spectrophotometer (Thermo Scientific Lumina). Time-resolved photoluminescence (TRPL) spectra were obtained using an Omin- \\u03bb monochromator/spectrometer with a time dependent single photon counting method (Zolix). Perovskite solar cells used for the measurements were not further encapsulated.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.79MA0.16PbBr0.51I2.49,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Perovskite material preparation (CsPbI3 and CsPbBr3), solar cell configuration and the energy level diagram of the materials used are shown in Fig. 1 (a\\u2013d), respectively. F-doped tin oxide (FTO) transparent conducting substrates (Pilkington TEC15) were cut and the edge of the FTO layer was first etched using Zn powder and HCl in order to eliminate shunting of the solar cell which was then cleaned by sequential 15\\u202fmin ultrasonic baths in aqueous detergent solution. The substrate was rinsed with water and ethanol and then treated with a UV/O3 cleaner for 15\\u202fmin. A compact \\u223c50\\u202fnm thin TiO2 was then applied to the clean substrate by spin coating using a solution of titanium di-isopropoxide bis(acetylacetonate) (TAA; 0.6\\u202fmL) in ethanol (9\\u202fmL, Aldrich) on a hot plate at 450\\u202f\\u00b0C.\\nCsPbI3 perovskite was prepared by solution process method as illustrated in Fig. 1(a). Freshly prepared PbI2 (4\\u202fg, Aldrich) was dissolved in 20\\u202fml of 48% aqueous hydrobromic (HBr, Aldrich) solution forming a pale yellow solution. To this solution was added CsI (2.5\\u202fg, TCI chemicals Pvt. Ltd.) dissolved in 10\\u202fml of H2O, resulting in the immediate precipitation of yellow color colloid. The colloid was suction filtered, copiously washed with diethyl either and dried under vacuum to obtain 5.2\\u202fg of pure CsPbI3 (\\u223c90% yield). The reaction is highly reproducible and scalable and can provide a source of pure CsPbBr3 for device fabrication purpose. CsPbBr3 was prepared by solution processing technique under the same condition. PbBr2 and CsBr were used as precursors and 15\\u202fml of HI was used for CsPbBr3 preparation. After the synthesis of CsPbI3 and CsPbBr3, subsequent solutions were prepared using N, N-dimethylformamide (DMF, Aldrich) and dimethylsulfoxide (DMSO, Aldrich) solvents for preparation of the doped samples, respectively.\\nFor preparation of the doped CsPbI3 thin film, 0.5\\u202fg CsPbI3 powder was dissolved in 2\\u202fml of DMF under stirring at 70\\u202f\\u00b0C, then, a desired concentration (10%) of the dopant was directly added into the above solution. Similarly, doped CsPbBr3 thin film prepared by dissolving 0.5\\u202fg of CsPbBr3 powder in 2\\u202fml DMSO was stirred at 70\\u202f\\u00b0C for 30\\u202fmin with desired concentration of the dopant. After completely dissolving, the solutions were spin-coated on preheated (50\\u202f\\u00b0C) substrates for 30\\u202fs at 3000\\u202frpm and were then dried on a hot plate at 120\\u202f\\u00b0C for 30\\u202fs in air. CuSCN was then deposited by \\u2018doctor blading\\u2019 at 70\\u202f\\u00b0C. The solution was prepared by dissolving 6\\u202fmg CuSCN (Aldrich) in 1\\u202fml propylsulfide. Finally, 50\\u202fnm thick of gold was evaporated on top as the back contact.\\nThe crystal structures of the perovskite films were analyzed by X-ray diffraction (XRD; Miniflex II, Rigaku). The absorption spectra of mesoporous and planar perovskite films were characterized by UV/vis spectrophotometer (Lambda 750, PerkinElmer). Scanning electron microscopy (SEM; JSM-6510, JEOL) was employed to evaluate the morphology and cross-sectional image of the films. The Fourier transform infrared (FT-IR) spectra have been recorded using Perkin Elmer Spectrum one FTIR over the region 4000\\u2013400\\u202fcm\\u22121 employing KBr pellet technique. Electron spin resonance (ESR) spectra of the pure and doped CsPbI3 and CsPbBr3 powders were measured using EPR spectrometer (Bruker EMXPlus) at room temperature. The photocurrent\\u2013voltage (J\\u2013V) characteristic of PSCs were measured with a Keithley 2400 source meter under the simulated AM 1.5G illumination with 500\\u202fW Xe lamp (YSS-80A, Yamashita Denso), from open circuit to short circuit with a scan rate of 0.2\\u202fV/s. The size of the samples used for photocurrent\\u2013voltage (I\\u2013V) measurements was 0.25\\u202fcm2. To consider the photovoltaic effects of the solar cells, the results of reverse bias voltage scans were eliminated because these can lead to overestimation of the results. Thus, all results presented here were obtained from the forward-bias voltage scans. The differential hole-transport resistance and recombination resistance (Rrec) were determined by electrochemical impedance spectroscopy (EIS) measurements in the dark at various bias voltages between 0.55 and 0.70\\u202fV with the frequency range of 0.1\\u202fHz\\u2013100\\u202fkHz. The EIS spectra were measured using a potentiostat (SP-150, Bio-Logic) and Zview2 software was used for the fitting. The given differential resistances represent the average for three different cells.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: Cu,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 0.5,\\n HTL_stack_sequence: CuSCN,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.25,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Ni(NO3)2\\u00b76H2O (99.9%) and CoCl2\\u00b76H2O (99.0%), PbI2 (99.9%) and CH3NH3I (MAI, 99.0%) were purchased from Kanto. [6,6]-Phenyl-C61-butyric acid methyl ester (PCBM, 99%) was purchased from Lumitec. 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP, 99%), anhydrous N,N-dimethylformamide (DMF, 99.8%), anhydrous dimethyl sulfoxide (DMSO, 99.8%) and chlorobenzene (CB, 99.8%) were all purchased from Wako. Ag (99.999%) was purchased from Nihon Materials.\\n\\nNiOx nanoparticles were prepared by a chemical precipitation method according to the report (Jiang et al., 2015). To prepare the pristine NiOx nanoparticles, Ni(NO3)2\\u00b76H2O (0.25\\u202fmol) was dissolved in 50\\u202fmL of deionized H2O to obtain a dark green solution. Under continuous magnetic stirring, the pH of the solution was adjusted to 10 by adding 10\\u202fM NaOH aqueous solution dropwise as the pH value was measured by a pH meter (Mettler Toledo). After being stirred for another 1\\u202fh, the green colloidal precipitate was collected by a centrifugation at 6000\\u202frpm for 10\\u202fmin, washed twice with deionized water and dried at 80\\u202f\\u00b0C for 6\\u202fh. The obtained green solid was calcined at 270\\u202f\\u00b0C for 2\\u202fh to obtain a black powder. For doping divalent cobalt (Co2+), CoCl2\\u00b76H2O was added to the Ni(NO3)2\\u00b76H2O solution at various molar ratios (0.5, 1, 2, 5 and 10\\u202fmol%) while the calcination temperature was set at 270\\u202f\\u00b0C. Before use, nanoparticles were dispersed in deionized water by sonication for 30\\u202fmin (20\\u202fmg\\u202fmL\\u22121). Finally, the nanoparticle solution was filtered through a PVDF filter (0.40\\u202f\\u03bcm).\\n\\nPatterned ITO-coated glass substrates (\\u223c10\\u202f\\u03a9 \\u25a1\\u22121) were cleaned with detergent water and then sonicated in deionized H2O, acetone and isopropyl alcohol sequentially each for 15\\u202fmin. After being dried with clean N2, the substrate was subjected to a UV-ozone treatment for 10\\u202fmin. The HTLs were obtained by spin-coating the corresponding NiOx or Co-NiOx aqueous solution (20\\u202fmg\\u202fmL\\u22121) at 3000\\u202frpm for 40\\u202fs and then annealed at 130\\u202f\\u00b0C for 10\\u202fmin to remove residual water. According to the spectroscopic ellipsometry measurements (J. A. Woolman, M-2000U), the average thickness of NiOx films was ca. 30\\u202fnm (Chen et al., 2015). All of the above procedures were carried out under air. After the NiOx or Co-NiOx films were cooled to room temperature, the substrates were then transferred into a nitrogen-filled glovebox. Equal moles of PbI2 (996\\u202fmg) and MAI (343\\u202fmg) were dissolved in 1.5\\u202fmL of a mixed solvent of DMF and DMSO (the volume ratio of DMF/DMSO was 6:1) to obtain the perovskite precursor solution, which was filtered through a PTFE filter (0.22\\u202f\\u03bcm). The solution was spin-coated on top of the NiOx layer at 1000\\u202frpm for 12\\u202fs and 5000\\u202frpm for 30\\u202fs and at the initial 19\\u202fs after starting the rotation, 800\\u202f\\u03bcL of CB was quickly dropped onto the centre of the rotating substrate. The film was then annealed on a hot plate at 100\\u202f\\u00b0C for 10\\u202fmin to obtain dark brown MAPbI3 films (400\\u202fnm). Afterward, PCBM (20\\u202fmg\\u202fmL\\u22121 in CB) was spin-coated at 1000\\u202frpm for 30\\u202fs and dried at 60\\u202f\\u00b0C for 10\\u202fmin. BCP (0.5\\u202fmg\\u202fmL\\u22121 in acetonitrile) was deposited by spin-coating at 6000\\u202frpm for 30\\u202fs and dried at 60\\u202f\\u00b0C for 5\\u202fmin. Finally, Ag electrodes with a thickness of 100\\u202fnm were thermally evaporated at a deposition rate of about 0.5\\u202fnm\\u202fs\\u22121 in a vacuum chamber (base pressure\\u202f<\\u202f9\\u202f\\u00d7\\u202f10-4 Pa) through a shadow mask.\\n\\nThe X-ray diffraction (XRD) spectra of the NiOx powder were taken by an X-ray diffractometer (Rigaku MiniFlex600) at a scanning rate of 1\\u00b0 min\\u22121 using the Cu K\\u03b1 radiation (1.540598\\u202f\\u00c5). Spectra were acquired with a D/teX Ultra2 detector for 2\\u03b8\\u202f=\\u202f5\\u00b0\\u202f\\u2212\\u202f70\\u00b0 at a step width of 0.02\\u00b0 in a source slit width of 1\\u202fmm. Elemental analysis was carried out by X-ray photoelectron spectroscopy (XPS, ULVAC-PHI, Inc., QuanteraSXM). Ultraviolet photo-electron spectroscopy (UPS) was measured with a Rikaken Keiki AC-3 spectrometer. Transmission electron microscopy (TEM) images were recorded using a JEOL-2100F microscope and an internal charge-coupled device camera. The average fringe distance in high-resolution TEM (HRTEM) images was measured by the Digital Micrograph (DM) software. The surface morphological observations of NiOx, Co-NiOx and perovskite films were made by field-emission scanning electron microscopy (SEM, Hitachi FE-SEM SU83230) and atomic force microscopy (AFM, SII L-trace). Steady state photoluminescence (PL) and time-resolved photoluminescence (TRPL) were measured by a Hamamatsu C12132 fluorescence lifetime spectrometer using a 1.5\\u202fns pulsed laser (frequency 15\\u202fkHz) at an excitation wavelength of 532\\u202fnm and an excitation power of 1 mW. The current-voltage characteristics were measured using a metal mask with an area of 1.02\\u202fcm2 under AM1.5 sunlight (100 mW cm\\u22122, WXS-155S-10\\nWacom Denso Co. Japan). The incident photon-to-current efficiency (IPCE) spectra were measured with a monochromatic incident light of 1\\u202f\\u00d7\\u202f1016\\u202fphotons\\u202fs\\u22121\\u202fcm\\u22122 in the direct current mode (CEP-2000BX, Bunko Keiki).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-np,\\n HTL_additives_compounds: Co,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 1.02,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Titanium (IV) chloride (TiCl4, 99.9%); Benzyl alcohol (BzOH, 98%); anhydrous ethanol (99.8%); lead (II) iodide (PbI2, 99%), lead(II) bromide (PbBr2, 99.9%), cesium iodide (CsI, 99.9%), methylammonium bromide (MABr), bis(trifluoromethane)sulfonimidelithium salt (Li-TFSI), 4-tert-butylpyridine (tBP), dimethylformamide (DMF), dimethyl sulfoxide (DMSO), chlorobenzene, and titanium diisopropoxide bis(acetylacetonate) were purchased from Sigma-Aldrich and used as received. Spiro-MeOTAD was purchased from 1-materials company. Formamidinium iodide (FAI), and FK209 (tris[2-(1H-pyrazol-1-yl)-4-tert-butylpyridine]cobalt(III) tris[bis(trifluoromethyl-sulfonyl)imide]) were purchased from Dyesol.\\n\\nThe TiO2 NPs were synthesized following a previously reported non-hydrolytic sol-gel process with some modification (Tan et al., 2017; Zhou et al., 2014). TiCl4 solution was mixed drop by drop into cold anhydrous ethanol with rapid stirring in an ice bath to avoid overheating. After the solution became transparent, extra anhydrous ethanol was added to the stock solution to realize 2.0\\u202fM TiCl4 concentration. Benzyl alcohol (80\\u202fml) was mixed with 20\\u202fml 2.0\\u202fM TiCl4 solution in a 250\\u202fml round bottom flask, and maintained without stirring at 70\\u202f\\u00b0C for various reaction times: 2, 4, 6, 8, 10, and 12\\u202fh. The solution was then diluted with ethanol and transparent products collected by centrifuge.\\n\\nBenzyl alcohol (80\\u202fml) was mixed with 2.0\\u202fM TiCl4 stock solution (20\\u202fml) in a 250\\u202fml round bottom flask and then NbCl5 added at dopant range 1\\u20135\\u202fmol%. The fully dissolved reaction solution was heated without stirring and held at 70\\u202f\\u00b0C for 6\\u202fh. The final solution was then diluted by ethanol and transparent products collected by centrifuge.\\n\\nHT-TiO2 film was prepared from 0.2\\u202fM titanium diisopropoxide dis(acetylacetonate) in 1-butanol by spin coating at 4000\\u202frpm, and then annealed at 500\\u202f\\u00b0C for 30\\u202fmin in a furnace. The resulting TiO2 film was treated with 40\\u202fmM aqueous TiCl4 solution at 70\\u202f\\u00b0C for 45\\u202fmin and then cleaned with distilled water and annealed at 500\\u202f\\u00b0C for 10\\u202fmin in a furnace.\\n\\nThe PSCs were fabricated with glass/FTO/ETL/perovskite/Spiro-MeOTAD/Au structure. First, cleaned FTO coated glass substrates were treated with UV/ozone for 30\\u202fmin and an LT-TiO2 layer was deposited by spin coating at 2000\\u202frpm from synthesized monodisperse LT-TiO2 NPs solution (see Section 2.2) to provide ETL. The resultant films were sintered at different temperatures between 50 and 250\\u202f\\u00b0C for 30\\u202fmin on a hot plate and UV/ozone treated for 15\\u202fmin. The film thickness of ETLs were measured to be 40\\u201360\\u202fnm. Triple mixed cation based perovskite (Cs0.05(MA0.15FA0.85)0.95Pb(I0.85Br0.15)3) precursor solution was prepared following a previously published method (Saliba et al., 2016), and spin-coated in a two-step process at 1000 and 5000\\u202frpm for 10 and 30\\u202fs, respectively. During the second step, 500\\u202f\\u03bcL of chlorobenzene (CB) was poured on the spinning substrate 10\\u202fs prior to the end of the program. The films were then sintered at 100\\u202f\\u00b0C for 45\\u202fmin under controlled relative humidity (RH\\u202f\\u2248\\u202f22%). Hole extracting material solution was prepared by dissolving 30\\u202fmg Spiro-MeOTAD, 21.5\\u202f\\u00b5L dilute 4-tert-butylpyridine (1\\u202fml 4-tert-butylpyridine mixed with 1\\u202fml of acetonitrile), 21.5\\u202f\\u00b5L stock solution (170\\u202fmg\\u00b7ml\\u22121 lithium bis(trifluoromethylsulphonyl)imide in acetonitrile), and 6\\u202f\\u00b5L stock solution (300\\u202fmg\\u202fml\\u22121 FK209 (tris[2-(1H-pyrazol-1-yl)-4-tert-butylpyridine]cobalt(III) tris[bis(trifluoromethylsulfonyl)imide]) in acetonitrile) in 1\\u202fml anhydrous chlorobenzene. The Spiro-MeOTAD solution was spin coated onto the perovskite film at 3000\\u202frpm. Finally, an Au anode (100\\u202fnm) was thermally deposited under high vacuum (<5\\u202f\\u00d7\\u202f10\\u22127\\u202fTorr) using a shadow mask to create devices with total area\\u202f=\\u202f0.22\\u202fcm2.\\n\\nWe obtained UV\\u2013Vis absorption and photoluminescence (PL) spectra for the spin coated films using a UV\\u2013Vis spectrophotometer (Scinco, S-3100, Korea) and Varian Cary Eclipse fluorescence spectrophotometer with 15\\u202fW Xenon lamp, respectively. Time-resolved PL (TRPL) traces were recorded using a time-correlated single photon counting (TCSPC) system (FL920, Edinburgh Instruments) with 40\\u202fnm pulsed laser source. All samples were excited from the bottom perovskite side at 464\\u202fnm and 770\\u202fnm emission wavelength was recorded in ambient conditions. X-ray photoelectron spectroscopy (XPS) and ultraviolet photoemission (UPS) spectra were collected using a Sigma Probe.\\n\\nElectrical characteristics were measured using a solar simulator LAB50 (MacScience) with attached Keithley under 1 sun in ambient conditions. Incident photon to converted electron (IPCE) efficiency was measured using photomodulation spectroscopy (McScience, K3100 Spectral IPCE Measurement System) with monochromatic light from a Xenon lamp. The monochromatic light power density was calibrated using a Si photodiode certified by the National Institute for Standards and Technology. Light intensity dependent J\\u2013V characteristics were measured using the same solar simulator setup by varying light intensity from 0.1 to 1 sun.\\n\\nField emission scanning electron microscope (FESEM) images were obtained using a JSMJSM-6700F (JEOL) device, and one-dimensional X-ray diffraction (1D-XRD) was performed using a Rigaku D/Max-2500 diffractometer with Cu-K\\u03b1 x-rays.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.81MA0.14PbBr0.45,\\n Perovskite_composition_short_form: CsFAMAPbBr,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.22,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemical reagents were purchased from Sigma-Aldrich and used without further operation, unless otherwise stated. Formamidinium iodide (FAI) and methylammonium bromide (MABr) salts were obtained from Xi'an Polymer Light Technology Corp, China. Spiro-OMeTAD was supplied by Luminescence Technology Corp, Taiwan, China. FTOs with sheet resistance of 15\\u202f\\u03a9\\u202fsq\\u22121 (Nippon Glass Corp, Japan) were used as conductive substrates.\\n\\nSnO2 and Y-SnO2 NCs were synthesized with solvothermal method. For synthesis of SnO2 NCs, a mixture containing 7\\u202fmL OA, 20\\u202fmL cyclohexane, 1.0\\u202fg Tin (IV) chloride pentahydrate and 5\\u202fmL triethylamine was added into a 50\\u202fmL autoclave and reacted at 180\\u202f\\u00b0C for 24\\u202fh. After cooled down to room temperature, 50\\u202fmL ethanol was added to precipitate the products, which were further centrifuged at a rate of 12,000\\u202frpm for 10\\u202fmin. Finally, the SnO2 NCs were re-dispersed in toluene with concentration of 20\\u202fmg\\u202fmL\\u22121. For synthesis of Y-SnO2 NCs, in addition to 7\\u202fmL OA, 20\\u202fmL cyclohexane, 1.0 g Tin (IV) chloride pentahydrate and 5\\u202fmL triethylamine, 6.16, 9.25, 12.33 and 15.41\\u202fmg Yttrium (III) butoxide from 40, 60, 80 and 100\\u202f\\u00b5L toluene solution [containing 0.5\\u202fM Yttrium (III) butoxide], respectively, were added into the reaction solutions. Correspondingly, the mole ratios of Y/Sn are 0.71\\u202f\\u00d7\\u202f10\\u22122, 1.06\\u202f\\u00d7\\u202f10\\u22122, 1.42\\u202f\\u00d7\\u202f10\\u22122 and 1.77\\u202f\\u00d7\\u202f10\\u22122 in these reaction solutions. And then the solvothermal reaction and centrifugation were done with the same methods as abovementioned. Finally, the Y-SnO2 NCs were re-dispersed in toluene with concentration of 20\\u202fmg\\u202fmL\\u22121.\\n\\nThe SnO2 and Y-SnO2 ETLs were prepared on the laser-patterned FTOs with size of 1.5\\u202f\\u00d7\\u202f1.5\\u202fcm2. The impurities on the FTOs were carefully cleaned out with isopropanol, acetone, distilled water and ethanol in order. And then, the cleaned FTOs were treated with UV-ozone for 30\\u202fmin.\\nThe 1\\u202fmL toluene dispersion of as-synthesized SnO2 or Y-SnO2 NCs (20\\u202fmg\\u202fmL\\u22121) was dropped on the patterned and cleaned FTOs and spin-coated at 4000\\u202frpm for 30\\u202fs. And then, the substrates were heated at 150\\u202f\\u00b0C for 30\\u202fmin to form SnO2 or Y-SnO2 ETLs. Later, the Cs0.05(MA0.15FA0.85)0.95Pb(I0.85Br0.15)3 perovskite films were prepared on the SnO2 or Y-SnO2 ETLs. In details, 200\\u202f\\u00b5L of Cs0.05(MA0.15FA0.85)0.95Pb(I0.85Br0.15)3 perovskite precursor solution dissolved in a mixed solvent of anhydrous N,N-dimethylformamide (DMF) and dimethyl sulphoxide (DMSO), the volume ratio of DMF/DMSO was 4/1 and the molar ratios of PbI2/PbBr2, FAI/MABr, CsI/(FAI\\u202f+\\u202fMABr) and (FAI\\u202f+\\u202fMaBr\\u202f+\\u202fCsI)/(PbI2\\u202f+\\u202fPbBr2) were 0.85/0.15, 0.05/0.95 and 1/1, respectively, was spin-coated at 1000\\u202frpm for 10\\u202fs following with 6500\\u202frpm for 20\\u202fs. 130\\u202f\\u00b5L of chlorobenzene was poured on the spinning substrate as an anti-solvent with the procedure lasting for 25\\u202fs. This was followed by annealing at 100\\u202f\\u00b0C for 50\\u202fmin.\\nThe spiro-OMeTAD solution containing 72.3\\u202fmg spiro-OMeTAD, 28.8\\u202f\\u03bcL 4-tert-butyl pyridine and 17.5\\u202f\\u03bcL lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520\\u202fmg Li-TSFI dissolved in 1\\u202fmL acetonitrile) and 1\\u202fmL chlorobenzene was prepared firstly, and then 20\\u202f\\u03bcL of the as-prepared spiro-OMeTAD stock solution was spin-coated on the perovskite layers at 4000\\u202frpm for 30\\u202fs. Finally, 100\\u202fnm Au electrodes were thermally evaporated on the spiro-OMeTAD layers under high vacuum through a shadow mask.\\n\\nA Bruker D8 Advance X-ray diffractometer with Cu K\\u03b1 radiation (\\u03bb\\u202f=\\u202f1.5418\\u202f\\u00c5) was used to detect the XRD patterns. A SU8000 SEM and a JEM-2100 TEM were used to observe the morphologies of the samples. An EDS (Oxford Inca) was used to characterize the elements in the samples. A photoelectron spectrometer (ESCALAB 250 Xi, Thermo Fisher Scientific) was used to measure the XPS and UPS spectra of the samples. A Lamda 950 UV\\u2013Vis-NIR spectrophotometer was used to measure the absorption and transmittance spectra of the samples. A fluorescence spectrophotometer (Thermo Fisher Scientific) was used to measure the PL spectra with a Xenon lamp as light source and the excitation wavelength of 460\\u202fnm. An Omin-\\u03bb Monochromator/Spectrograph (Zolix) with the time-correlated single-photon counting method (Pico harp 300) was used to record the TRPL spectra, and the samples were excited by 507\\u202fnm wavelength at room temperature with 120\\u202fnJ\\u202fper\\u202fcm2 per pulse from a pulsed laser diode. The TRPL decay curves were fitted by a bi-exponential equation (Eq. (1)) as follows (Jung et al., 2017): It=\\u2211iAiexp-t/\\u03c4i where Ai is the decay amplitude and \\u03c4i is the decay time. The average PL decay time (\\u03c4ave) can be calculated with the fitted Ai and \\u03c4i values according to the Eq. (2) as follows (Wen et al., 2016): \\u03c4avg=\\u2211Ai\\u03c4i2\\u2211Ai\\u03c4i\\nA PVIV-94043A (Newport, USA) solar simulator with AM 1.5 G and 100\\u202fmW\\u202fcm\\u22122 solar illumination, which was adjusted using a NREL-calibrated Si solar cell equipped with KG-2 filter, combining with a computer-controlled Keithley 2400 source meter was used to measure the J-V characteristic curves of PSCs, respectively. The voltage step and delay time were 20\\u202fmV and 10\\u202fms, respectively. The forward scan started from \\u22120.1\\u202fV to 1.2\\u202fV, while reverse scan from 1.2\\u202fV to \\u22120.1\\u202fV. The stabilized current density and power output were recorded close to the maximum power point, which was extracted from the J-V characteristic curves. The PSCs with the active area of 0.12\\u202fcm2 (calibrated with a black metal mask with the area of 0.3\\u202f\\u00d7\\u202f0.4\\u202fcm2) and without any encapsulation were prepared for measurements. The J-V characteristic curves for evaluating the conductivity of the ETLs and the trap-state density of perovskites on the ETLs were also recorded with the same Keithley 2400 source meter in the dark with FTO/ETL/Au architecture and electron-only devices, respectively.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.81MA0.14PbBr0.45I2.55,\\n Perovskite_composition_short_form: CsFAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 50,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The materials and chemicals used in the PSC fabrication were purchased from commercial sources as: lead (II) iodide (PbI2, 99.999%), dimethylformamide (DMF), dimethyl sulfoxide (DMSO), titanium diisopropoxide bis(acetylacetonate), anhydrous ethanol, ethanol, isopropyl alcohol, 1-butanol, toluene, chlorobenzene, acetonitrile, 4-tert-butylpyridine (TBP), and bis(trifluoromethylsulfonyl)-imide lithium salt (Li-TFSI) from Sigma-Aldrich. TiO2 paste (30NR), methyl ammonium iodide (MAI, 99.9%), tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) tris(bis(trifluoromethylsulfonyl)imide) (FK209) from Dyesol and 2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-p-methoxyphenylamine)-9,9\\u2032-spirobifluorene (Spiro-OMeTAD) from Lumtec. All chemicals were used as received.\\n\\nThe normal structure of the PSCs was fabricated with stack as glass/FTO/ETL/MAPbI3/Spiro-OMeTAD (100\\u202fnm)/Au (80\\u202fnm). FTO substrates were thoroughly cleaned with soap solution, deionized water, ethanol, and isopropanol for 20\\u202fmin each in sequence under sonication. After cleaning, N2 was flushed through the substrates and transferred to oven at 70\\u202f\\u00b0C for two hours. Then substrates were cleaned with UV-ozone treatment for 20\\u202fmin. The cleaned substrates were spin-coated with solution of titanium diisopropoxide bis(acetylacetonate) (0.3\\u202fM) in 1-butanol at 2000\\u202frpm for 20\\u202fs to form c-TiO2 layer. c-TiO2 coated substrates were annealed at 120\\u202f\\u00b0C for 10\\u202fmin and then sintered at 500\\u202f\\u00b0C for 20\\u202fmin. Thickness of c-TiO2 layer was controlled by double (2c-TiO2) and triple (3c-TiO2) coating of the above solution. On the top of c-TiO2 layer, m-TiO2 layer was coated by using a commercial TiO2 paste (30NR) diluted in anhydrous-ethanol with 1:10 (w:w) at 3000\\u202frpm for 30\\u202fs followed by 500\\u202f\\u00b0C sintering for 30\\u202fmin in furnace. After ETL deposition, all the substrates were treated with 0.2\\u202fM solution of TiCl4 (2\\u202fM) prepared in deionized water. Substrates were dipped in this solution and were held at 70\\u202f\\u00b0C for 30\\u202fmin. After that, all the substrates were cleaned with deionized water and N2 was flushed through them exhaustively. Then, the substrates were heated at 500\\u202f\\u00b0C for 35\\u202fmin. A mixed PbI2 (1M) and MAI (1M) precursor solution prepared in 1\\u202fmL of mixed solvent of anhydrous DMF:DMSO (4:1) and stirred at 65\\u202f\\u00b0C for overnight. The perovskite film was formed by spin coating precursor solution on the top of different ETLs through two-step spin coating program (10\\u202fs at 1200\\u202frpm and 20\\u202fs at 4000\\u202frpm) with dripping of toluene as anti-solvent during the second step, 10\\u202fs before the end. The perovskite films were annealed at 100\\u202f\\u00b0C for 15\\u202fmin. The Spiro-OMeTAD (73\\u202fmg\\u202fmL\\u22121 in chlorobenzene) was doped by 28\\u202f\\u00b5L, 28\\u202f\\u00b5L, and 18\\u202f\\u00b5L of TBP, FK209 (mother solution of 300\\u202fmg/ml of acetonitrile), and Li-TFSI (mother solution of 530\\u202fmg/ml of acetonitrile), respectively. This Spiro-OMeTAD solution was spin-coated at 3000\\u202frpm for 30\\u202fs as hole transport layer. An 80\\u202fnm thick Au top electrode was deposited by using thermal evaporator at a high vacuum.\\n\\nUV\\u2013vis absorption and PL spectra for all the films were measured using a Scinco UV\\u2013visible spectrophotometer (S-3100, Korea) and Varian Cary Eclipse fluorescence spectrophotometer with 15\\u202fW Xenon lamp, respectively. Field emission scanning electron microscope (FESEM) images were obtained using JSMJSM-6700F (JEOL) FESEM. One dimensional X-ray diffraction (1D-XRD) measurements were recorded using X-ray diffractometer (Rigaku D/Max-2500) with Cu-K\\u03b1 X-rays. The different ETL layer thickness was determined by cross-sectional FESEM and alpha-step (D-300, Stylus) profilometer.\\n\\nThe electrical characteristics were measured with a solar simulator LAB50 (McScience) for a one-sun condition along with attached Keithley. The light was calibrated with a standard mono-Si solar cell (PVM-396, PV Measurements Inc.) certified by the National Renewable Energy Laboratory (NREL). The incident photon-to-current conversion efficiency (IPCE) spectrum was measured using a photomodulation spectroscopy setup (McScience, K3100 Spectral IPCE Measurement System) with monochromatic light from a Xenon lamp. The power density of the monochromatic light source was calibrated using a Si photodiode certified by the National Institute for Standards and Technology. Light intensity (I) -dependent J-V characteristics were measured with the same solar simulator setup by varying the sun intensity from 10\\u2013100\\u202fmW\\u202fcm\\u22122.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}]"
  },
  {
    "path": "SII_MDP/data/sii40.json",
    "content": "[{\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The information of all materials and the preparation of precursor solutions are provided in Supplementary material, also can be found in our previous report . ITO-coated glass with a sheet resistance of 10\\u202f\\u03a9 sq-1 was ultrasonically cleaned by detergent, deionized water in sequence. PEDOT:PSS was spin-coated onto the ITO substrates at 3000\\u202frpm followed by baking at 120\\u202f\\u00b0C for 20\\u202fmin in the air. The same process parameters of spin-coating are suitable for DMSO-doped PEDOT:PSS. The mixed lead precursor solution was preheated at 90\\u202f\\u00b0C on a hot plate and spin-coated at 6000\\u202frpm onto the ITO/PEDOT:PSS substrates. The ITO/PEDOT:PSS substrates were preheated and kept at 40\\u202f\\u00b0C during the whole spin-coating process, which was realized by using the spin-coater with the function of substrate-preheating. And then the MAI precursor solution with different 1,6-DD content (0\\u202fwt%, 0.025\\u202fwt%, 0.05\\u202fwt%, 0.075\\u202fwt%, and 0.1\\u202fwt%) was dropping-coated, waiting for 30\\u202fs after the liquid spreading evenly, and spin-coated at 6000\\u202frpm followed annealing at 90\\u202f\\u00b0C for 40\\u202fmin. Then PCBM:BCP blend solution was spin-coated on the perovskite film at 1000\\u202frpm. Finally, Ag metal layer was deposited by thermal evaporation through a shadow mask which determined the cell area of 0.1\\u202fcm2. Except for the perovskite preparation process was performed in an argon-filled glove box, almost all solution processes were performed in the air.\\n\\nX-ray diffraction (XRD, Rigaku D/MAX 2500) with Cu K\\u03b1 radiation was carried out to record the crystal structure of the perovskite film. Ultraviolet-visible spectroscopy (UV\\u2013vis) of perovskite film was observed with a Jasco-4000 spectrophotometer. The film surface morphology of the final perovskite films were investigated by field-emission scanning electron microscope (SEM, Hitachi SU-8010), atomic force microscopy and conducting atomic force microscopy (AFM and C-AFM, Bruker INNOVA SPM). The film thickness was recorded by KLA-Tencor AlphaStep D-100 Stylus Profiler. Steady-state photoluminescence spectra (PL) and time-resolved photoluminescence of spectra (TRPL) the film were recorded with a Jobin Yvon FluoroLog-3 fluorescence spectrometer to explore the defect passivation and nonradiative recombination. Electrochemical Impedance Spectroscopy (EIS) measurements (Zahner-Zennium equipment) were performed in a frequency range from 1\\u202fHz to 500\\u202fMHz to investigate the interfacial contact and charge transport. X-ray photoelectron spectroscopy (XPS) characterization were conducted by Thermo Scientific ESCALAB250Xi. Contact angle and surface energy measurements were recorded with Drop Shape Analyzer (Kr\\u00fcss DSA25S). The current density-voltage (J-V) characteristics of the devices were measured in an argon-filled glove box, with a programmed Keithley 2400 sourcemeter under illumination of a Newport Oriel 150\\u202fW solar simulator (AM 1.5G, 100\\u202fmW\\u202fcm-2). The light intensity of the solar simulator was calibrated with a solar reference cell (SRC-1000-TC-QZ, VLSI standards, Inc.). All devices were kept in the air without encapsulation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: BCP; PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 40,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: DMSO,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless otherwise stated, all chemicals were purchased from Sigma Aldrich and used as received. PCBM (phenyl-C61-butyric acid methyl ester, >99%) and PEDOT:PSS aqueous solution were purchased from Lumtec. PbI2 (99.9985%) was obtained from Alfa Aesar. Formamidinium iodide (FAI, CH(NH2)2I) and methylammonium bromide (MABr, CH3NH3Br) were acquired from Dyesol.\\n\\nPCBM was dissolved in chlorobenzene to the concentration of 20 mg mL\\u22121 and was stirred for 60 min. Triton X-100 was added to the PCBM solution with different weight percentages with respect to PCBM (1, 3, and 5 wt%) and stirred for 60 min. The homogeneously mixed surfactant-modified PCBM (s-PCBM) solution was filtered using a polytetrafluoroethylene (PTFE) filter (pore size: 0.45 \\u03bcm) and used as an electron transport material for perovskite solar cells.\\n\\nThe PSCs were fabricated on patterned, fluorine-doped tin oxide (FTO)-coated glass with a sheet resistance of 15 \\u03a9 sq\\u22121 (Pilkington). FTO substrates were cleaned sequentially in deionized (DI) water, acetone, and 2-propanol for 60 min using an ultra-sonication bath. A NiOX hole transport layer (HTL) was deposited by spin-coating a NiOX nanocrystal (NC) dispersion solution at 3000 rpm. NiOX NCs were synthesized according to the procedures reported elsewhere. Briefly, 0.05 mol of nickel nitrate hexahydrate (Ni(NO3)2\\u00b76H2O) was dispersed in 20 mL of DI water. Then 6 mL of NaOH solution (10 mol L\\u22121) was slowly dropped into the solution to obtain a large amount of precipitation and stirred for 30 min. The precipitate was washed with deionized water three times, and dried at 80 \\u00b0C. The obtained cyan powder was then calcined at 300 \\u00b0C for 2 h (ramping rate: 5 \\u00b0C min\\u22121) to produce a black NiOX powder. The obtained NiOX NCs were dispersed in DI water to 15 mg ml\\u22121 concentration. A perovskite precursor solution was prepared by dissolving 172 mg of FAI, 22 mg of MABr, 507 mg of PbI2, and 73 mg of PbBr2 in 1 mL of DMF/DMSO (v/v = 4/1) mixed solvent, and stirred at 60 \\u00b0C. The perovskite precursor solution was spun-cast at 1000 rpm for 10 s and 5000 rpm for 25 s on the pre-heated substrate at 40 \\u00b0C, under a N2 atmosphere. During the second spin-coating step, 0.3 mL of chlorobenzene was dripped onto the center of the substrate to promote perovskite film crystallization. After the whole spin-coating process, the substrate was annealed at 100 \\u00b0C for 20 min to form FA0.83MA0.17Pb(I0.83Br0.17)3 films. The electron transport layer was spin-coated from a PCBM solution (20 mg mL\\u22121 in chlorobenzene) or as-prepared s-PCBM solution at 3000 rpm for 30 s. Finally, a 60 nm-thick Au electrode was deposited by thermal evaporation. The active area of the fabricated device was 0.09 cm2.\\nFor PEDOT:PSS-based PSCs, a HTL was formed by spin-coating a PEDOT:PSS aqueous solution at 5000 rpm on a FTO substrate, and annealed at 125 \\u00b0C for 20 min. Further fabrication procedures were the same as those for the NiOX-based PSCs.\\n\\nAtomic force microscopy (AFM) images were acquired using an Park NX10 (Park Systems) and analyzed with XEI AFM data analysis software. Transmission electron microscopy (TEM) images were obtained using a JEM 2100 (JEOL). Field-emission scanning electron microscopy (FE-SEM) images were obtained using a JSM-6701F (JEOL). Photoluminescence spectra of the perovskite samples were recorded using an LS 45 fluorescence spectrometer (PerkinElmer, USA). Electrochemical impedance spectra (EIS) of the devices were measured by Zive Labs (Wonatech). The J\\u2013V characteristics of the devices were measured using an I\\u2013V tracer (MP-160, Eko Instruments) under standard AM 1.5G (100 mW cm\\u22122) illumination from a 500 W xenon lamp, calibrated with a KG5-filtered Si reference cell (K801, McScience Inc.). The external quantum efficiency (EQE) was acquired from 350 nm to 850 nm using a K3100 IPCE Measurement System (McScience Inc; chopping frequency of 4 Hz, without bias light and 10 nm step wavelength).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Triton X-100,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FA0.83MA0.17PbBr0.51I2.49,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: NiO-np,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (CH3NH3I) was synthesized and purified based on the method proposed by J. H. Im. All chemicals were used as received. Methylammonium iodide (CH3NH3I) was synthesized by mixing methylamine (CH3NH2) (27.8 mL, 0.273 mol, 40 wt% in methanol, Alfa Aesar) and hydroiodic acid (HI) (30 mL, 0.227 mol, 57 wt% in water, Alfa Aesar) in a 250 mL round-bottom flask, and stirring the mixture in an ice-water bath for 2 h. The yellowish raw product obtained by evaporating the solvent was recrystallized three times from a mixture of diethyl ether and ethanol. After filtration, the solid was collected in a dark container and dried at 60 \\u00b0C in a vacuum oven overnight. Anhydrous EuI2 was synthesized and purified based on the method proposed by Chengpeng D. Anhydrous EuI2 was prepared by dissolving europium oxide (Eu2O3) and ammonium iodide (NH4I) into HI to form a transparent solution. We obtained a dense solid after we evaporated the solution. Then the solid was placed into a quartz tube for vacuum dehydration in a tube heating furnace, until it was completely dehydrated. After that, the dehydrated solid was sintered until the solid turned to transparent melt. Eventually, anhydrous EuI2 in bulk polycrystalline was obtained.\\n\\nDevices were fabricated on fluorine-doped tin oxide (FTO) coated glass (Yingkou OPV Tech New Energy CO., LTD., OPV-FTO22-7). Initially, FTO was etched with 2 mol L\\u22121 HCl solution and zinc metal powder. Substrates were then cleaned sequentially by soap solution (2 vol% Hellmanex\\u2122 detergent), deionized water, acetone, ethanol, isopropanol (IPA) and UV exposure. Nickel(II) acetylacetonate was dissolved in ethanol (0.1 mol L\\u22121) with adding 5.3 \\u03bcL ethanolamine (38 wt%) into the solution. The solution was then stirred in a sealed glass vial in air overnight. Then the NiO solution was spin-coated onto the UV\\u2013ozone treated FTO substrate at 3000 rpm for 60 s and then annealed at 400 \\u00b0C for 60 min in ambient.\\nThe perovskite thin film was deposited by using a process similar to that described in a previous work. The MAPbI3:x% EuI2 (x = 0, 0.02, 0.04, 0.06, 0.08, 0.1) precursor solution was prepared by dissolving CH3NH3I (1 mmol), PbI2 (1.05 mmol; Alfa Aesar, 99.9985%) and EuI2 (a corresponding mass fraction of PbI2) in g-butyrolactone (GBL)/dimethyl sulfoxide (DMSO) (7:3; 1 mL) with a total concentration of 1 M and stirring at 70 \\u00b0C overnight. The perovskite thin films spread with 80 \\u03bcL was spin coated onto the FTO/NiO substrate followed by a two-stage spin-coating process at 1000 rpm for 15 s and 4000 rpm for 45 s. Then chlorobenzene (600 \\u03bcL; Alfa Aesar, 99%) was dripped as anti-solvent after 25 s the second stage to obtain a light-brown smooth film. Afterward, the perovskite film was annealed at 100 \\u00b0C for 10 min to convert to a dark-brown film. Subsequently, PCBM (15 mg dissolved in 1 mL chlorobenzene) was deposited on the cooled perovskites substrates by spin coating at 1500 rpm for 45 s, followed by the spin coating of BCP saturated solution in isopropanol. Finally, silver electrode (70 nm thick) was thermally evaporated on top of the device under high vacuum (<1 \\u00d7 10\\u22124 Pa). The active area of the device was 0.090 cm2, defined by the aperture area of the metal shadow mask.\\n\\nX-ray diffraction (XRD) patterns were obtained with Smart LAB instruments CuK\\u03b1 beam (\\u03bb = 1.54 \\u00c5). UV-vis absorption spectra measurement was carried out on a Hitachi U-3010 spectroscope, and was employed to assess the absorption properties of the doped perovskite sensitized NiO thin film. The morphology of the film was tested with scanning electron microscopy (SEM; JEOL JSM-7401F). The incident photon-to-electron conversion efficiency (IPCE) spectra were measured in air with equipment developed by the Institute of Physics, Chinese Academy of Sciences.\\nThe energy dispersive X-ray spectroscope (EDS) combined with a field-emission scanning electron microscope (SEM-EDS, EDAX Octane Pro). X-ray energies corresponded to I, Pb and Eu were collected as the SEM scanned the electron beam over the surface and cross-sectional area in FTO substrate. The X-ray data was synchronized with the SEM image and an \\u2018element image\\u2019 was created showing the presence of the selected element throughout the selected area.\\nThe current density\\u2013voltage (J\\u2013V) curves were measured with a 2400 Series SourceMeter (Keithley Instruments) under simulated AM 1.5 sunlight at an equivalent to 100 mW cm\\u22122 irradiance generated by an thermo oriel 91192-1000 simulator, with the intensity being calibrated with an VLSI standards incorporated PN 91150V Si reference cell. The mismatch factor was calculated to be less than 1%. The solar cells were masked with a metal aperture to define the active area, typically 0.090 cm2. The backward bias for stability characterization of the solar cell was held to 0.75 V. The as-prepared solar cells were stored at 25 \\u00b0C in light with a relative humidity (RH) of 30 \\u00b1 5% for the characterization of ambience stability. The specific PCE as a function of time was obtained with conventional environment treatment for 13 days in order to clarify the PCE evolution of solar cells.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All chemicals were used as received without purification, including PbI2 (99.9985%, Alfa Aesar), CH3NH2 (40 wt% aqueous solution, J&K Scientific), HI (57% w/w aqueous solution, Alfa Aesar), C60 (99.5%, HanFeng Chemical), [6,6]-phenyl-C61-butyric acid methyl ester (PCBM, 99%, Solenne BV), 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP, >99%, P-OLED), dimethylformamide (DMF, 99.9%, J&K Scientific), 1,2-dichlorobenzene (98%, Alfa Aesar) and poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS, P VP. Al 4083, Heraeus). The sheet resistance of ITO (170 nm in thickness) was 11 \\u03a9 per square.\\nMethylammonium iodide (MAI) was synthesized by reacting 16 mL of CH3NH2 solution and 10 mL of HI solution in a 3-necked 100 mL round-bottom flask filled with argon at 0 \\u00b0C for 2 h with stirring. The solvent was removed using a rotary evaporator at 50 \\u00b0C. The pale yellow precipitate was recrystallized with ethanol twice, filtered and washed with enough ethyl ether to remove the yellow by-product. The white product was dried at 60 \\u00b0C in a vacuum oven for 24 h, weighed and stored in an argon-filled glove box before use.\\n\\nWe used Zn powder and concentrated HCl to pattern the ITO substrates. The part to be remained was covered with tapes during etching. The patterned ITO substrates were first ultrasonically cleaned in detergent, rubbed using cotton, and then rinsed with distilled water. After drying, the surface of ITO was treated under UV/O3 for 15 min.\\nThe PEDOT:PSS aqueous solution was filtered with a 0.45 \\u03bcm PVDF membrane before spin coating. PEDOT:PSS films with a thickness of 40 nm were spin-coated onto the ITO substrates at 3000 rpm for 60 s. The substrates were baked on a 120 \\u00b0C hot plate in air for 20 min. PbI2 (0.368 g) was dissolved in 1 mL of DMF, into which about 18.9 \\u03bcL of water was added. The mixture was stirred for 5 h on a 70 \\u00b0C hot plate, and then filtered with a 0.22 \\u03bcm nylon membrane before spin coating. PbI2 films with a thickness of 95 nm were spin-coated onto the PEDOT:PSS or ITO substrates, which were preheated to 50 \\u00b0C, at 8000 rpm for 30 s. The substrates were then baked on a 70 \\u00b0C hot plate in air for 10 min before being transferred onto the bottom plate maintained at 70 \\u00b0C.\\nFive milligrams of MAI powder was dissolved in 10 mL of ethanol. Then the solution was homogeneously sprayed onto the bottom surface of the top plate that was maintained at 80 \\u00b0C. The distance between the plate and nozzle was about 10 cm and the pressure of compressed air used for spraying was about 1.5 atm. Then the top plate was placed on top of the bottom plate in the desiccator.\\nThe PHP apparatus was then sealed and pumped down to a pressure of about 100 Pa. At the same time, the top and bottom plates were ramped up to nominal temperatures of 120 \\u00b0C and 130 \\u00b0C, respectively. The plates were maintained at the temperatures for desired times before refilling the apparatus with Ar.\\nPCBM films with a thickness of 20 nm were spin-coated with a PCBM solution in dichlorobenzene (26 mg mL\\u22121) onto the perovskite films at 2400 rpm for 30 s, and annealed at 110 \\u00b0C for 10 min in air. Then the films were transported into a glove box filled with Ar, in which C60 (20 nm, 0.1 nm s\\u22121), BCP (8 nm, 0.01 nm s\\u22121) and Al (150 nm, 1 nm s\\u22121) were deposited in sequence by thermal evaporation under a background pressure of about 1 \\u00d7 10\\u22125 Pa.\\n\\nMorphology and elemental analysis of films were investigated using a cold field emission scanning electron microscope (SEM, SU8010, Hitachi) equipped with an IXRF energy dispersive spectroscopy (EDS) system. Data were acquired with an accelerating voltage of 15 kV for the latter. X-ray emissions of Pb M\\u03b11 and I L\\u03b11 at 2.3455 keV and 3.9376 keV respectively are chosen for analysis. We chose Pb M\\u03b11 emission instead of Pb L\\u03b11 emission (at 10.5515 keV) because of the stronger peak intensity of the former. The measured atomic ratios of I/Pb were calibrated with that of PbI2, which is 2:1. UV-visible absorption of perovskite films in VSR was recorded with a UV-vis spectrometer (U-4100, Hitachi). X-ray diffraction (XRD) patterns of films were recorded using an X-ray diffractometer (Rigaku D/MAX 2500) with Cu K\\u03b1 radiation at 5\\u00b0 per min from 10\\u00b0 to 60\\u00b0. The local irradiance on the films under reaction was measured with a radiometer (FZ-A). The thicknesses of films and widths of channels were measured with a profiler (AlphaStep D-100).\\nCurrent density\\u2013voltage (J\\u2013V) curves were measured with a programmed Keithley 2400 sourcemeter under illumination of a Newport Oriel 150 W solar simulator (AM 1.5 G, 100 mW cm\\u22122). All tests were carried out in air without encapsulation. The light intensity of the solar simulator was calibrated with a solar reference cell (SRC-1000-TC-QZ, VLSI standards, Inc.). The scanning step and sweeping rate of bias were 10 mV and 0.2 V s\\u22121, respectively.\\n\\nFor the electrical resistance measurements, a channel about 250 \\u03bcm in width was first etched along the diagonal of an ITO substrate. We connected the edges of the ITO substrate with the external circuit using copper powder conductive paste. The PEDOT:PSS aqueous solution was diluted with water (10 V/V%) and then filtered with a 0.45 \\u03bcm PVDF membrane. PEDOT:PSS films were spin-coated onto the ITO substrates at 3000 rpm for 30 s. Afterwards, similar fabrication procedures were used except that the resistance of the films during the reaction was monitored in situ with a UT61E multimeter, which was connected to a computer for data recording (Fig. 7b).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> Ethanol,\\n Perovskite_deposition_procedure: Spin-coating >> Spray-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> Unknown,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> 150.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 1.5,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All syntheses were carried out under an inert atmosphere in 50 mL three-neck flasks connected to a standard Schlenk line set-up, according to a recently developed protocol, with minor modifications. In a typical preparation of WO3\\u2212x CNRs with an aspect ratio of \\u223c8, 0.3 mmol of WCl6 (99.9%, Aldrich), 9.5 mmol of ODE (90%, Aldrich), 4.5 mmol of OLAM (70%, Aldrich) and 4.5 mmol of OLAC (90%, Aldrich) were degassed together at \\u223c120 \\u00b0C for 1 h under vigorous stirring. The mixture was then slowly heated up to 310 \\u00b0C under N2 flow and kept at this temperature for 2 h. Finally, the heating source was removed and the system was allowed to naturally cool down. After the synthesis, the nanocrystals were induced to flocculate out of the crude reaction mixture upon addition of acetone, then recovered by centrifugation, and finally washed twice with acetone. The as-extracted and purified hydrophobic-capped CNRs were easily re-dissolved in anhydrous chloroform and stored under N2 in a glove box prior to further use.\\n\\nPatterned ITO-coated glass substrates (Visiontech) were cleaned by ultrasonication in deionized water, 2 propanol and acetone. The substrates were treated according to the following washing procedure: they were immersed into a 5:1:1 v/v mixture of double distilled Milli-Q water, hydrogen-peroxide (H2O2) and ammonia (NH3) at 80 \\u00b0C for 10 min to remove organic contamination, then rinsed 10 times with water prior to the next deposition steps. The WO3\\u2212x CNR coatings were fabricated under ambient laboratory conditions as follows. A solution of purified WO3\\u2212x CNRs in CHCl3 was spin-coated onto patterned ITO cleaned substrates at 2500 rpm for 30 s to form a WO3\\u2212x thin layer of \\u223c20 nm. A solution of acetic acid (AcOH) in methanol (4 M) was dispensed on top of the film and then spin-cast. The WO3\\u2212x coatings were irradiated with a continuous-wave ultraviolet (cw-UV) lamp (Bromograph Nuova Delta Elettronica mod. MF1030 Lamps Silvenia BL350 with excitation wavelength centered at 320\\u2013380 nm) positioned at a distance of 10 cm from the sample. This procedure was repeated until the desired film thickness (\\u223c40 nm) was reached (\\u223ctwo layers).\\nCH3NH3I (MAI) was synthesized according to a literature procedure. CH3NH2 (27.86 mL, 40% in methanol, TCI) and hydroiodic acid (30 mL, 57 wt% in water, Aldrich) were mixed at 0 \\u00b0C and stirred for 2 h. The precipitate was recovered after solvent evaporation at 50 \\u00b0C for 1 h. The product was washed with diethyl ether three times and finally dried at 60 \\u00b0C in a vacuum oven for 24 h.\\nTo prepare the CH3NH3PbI3 perovskite precursor solution (43 wt%), the as-synthesized MAI and commercial PbI2 (ultra-dry, 99.999%, Alfa Aesar) were dissolved in a mixture of dimethylformammide (DMF, \\u226599%; Sigma-Aldrich) and DMSO (DMSO, 99.8%; Sigma-Aldrich) at a DMF:DMSO:PbI2 8.2:1:1 w/w, then stirred at ambient temperature for 1 h. The CH3NH3PbI3 solution was spin-coated onto the WO3\\u2212x-coated ITO substrate by a single step procedure at a rate of 4000 rpm. for 25 s. Solvent dripping was made with a 250 \\u03bcL of toluene 14 s before the end of the spin-coating process. Eventually, the perovskite film was thermally annealed for 10 min at 100 \\u00b0C. After cooling to room temperature, a PC60BM (99.8%, Sigma Aldrich) solution (25 mg mL\\u22121 in chlorobenzene) was spin-coated on the perovskite layer at 1000 rpm for 60 s. The device cathode, consisting of a 0.5 nm-thick LiF layer and a 150 nm-thick Al layer, was thermally evaporated atop the device at a pressure of 5 \\u00d7 10\\u22126 mbar.\\n\\nXRD patterns were recorded with a D8-Discover Bruker diffractometer (3.3 kW) equipped with a Cu source (operated at 40/40 mA/kV), a Goebel mirror, an Eurelian cradle goniometer, and a scintillator detector. The samples for measurements were prepared by depositing CNRs from a concentrated colloidal solution onto silicon substrates, and then allowing the solvent to evaporate. XRD patterns were collected, in 2\\u03b8 scan mode with a fixed incident angle of 5\\u00b0, moving the detector over the 2\\u03b8 range 10\\u00b0\\u2013120\\u00b0 with a step size of 0.05\\u00b0.\\n\\nConventional TEM investigation was performed on the as-synthesized WO3\\u2212x CNRs with a JEOL JEM 1400Plus microscope, equipped with a GATAN Orius SC600 CCD camera and a W filament-source operating at 120 kV. The samples for TEM analysis were prepared by drop-casting a few drops of suitably dilute CNR solutions onto standard carbon-coated copper TEM grids in a N2-protected glove-box and allowing the solvent to evaporate. The as-prepared sample grids were then transferred into the TEM microscope.\\n\\nAFM characterization was obtained with a park scanning probe microscope (PSIA) operating in air and in a noncontact mode to reduce tip induced surface degradation. The image acquisition was performed in air at room temperature.\\n\\nSEM images of the samples were recorded with a Carl Zeiss Auriga40 Crossbeam instrument, equipped with a Gemini column and an integrated high efficiency In-lens detector, working at an applied acceleration voltage of 5 kV and a short acquisition time to avoid beam-damage of the samples, in high vacuum and high-resolution acquisition mode.\\n\\nUV-vis absorption spectra of the WO3\\u2212x films were recorded using a Perkin Elmer Lambda 1050 spectrophotometer at room temperature.\\n\\nStatic water contact angles were measured using the sessile drop method and a CAM 200 (KSV Instruments Ltd Finland) instrument. Solvent contact angles were measured on WO3\\u2212x samples treated in the same way as the WO3\\u2212x films destined for devices. The presented results correspond to an average of measurements performed onto many areas of three samples.\\n\\nThe devices were characterized using a Keithley 2400 Source Measure Unit and a calibrated Air Mass 1.5 Global (AM 1.5G) solar simulator (Newport 91160A) with an irradiation intensity of 100 mW cm\\u22122. The solar simulator irradiance was set to 100 mW cm\\u22122 using a thermopile radiant power meter with a fused-silica window (Spectra Physics Oriel, model 70260). The active area of the complete device was 0.04 cm\\u22122. All devices are tested using 100 mV s\\u22121 or 1000 mV s\\u22121 scan rates, under a nitrogen atmosphere at 22 \\u00b0C. A calibrated filtered Si diode (Newport, 91150V) served as the reference cell for J\\u2013V measurements.\\n\\nSteady-state and time-resolved photoluminescence were measured by an Edinburgh FLS920 spectrometer equipped with a Peltier-cooled Hamamatsu R928 photomultiplier tube (185\\u2013850 nm). An Edinburgh Xe900 450 W Xenon arc lamp was used as the exciting light source. Corrected spectra were obtained via a calibration curve supplied with the instrument. Emission lifetimes were determined with the single photon counting technique by means of the same Edinburgh FLS980 spectrometer using a laser diode as the excitation source (1 MHz, \\u03bbexc = 635 nm, 57 ps pulse width and about 30 ps time resolution after deconvolution with an excitation power of 0.52 mW cm\\u22122) and a Hamamatsu MCP R3809U-50 (time resolution 20 ps) as detector. Perovskite thin films sealed with a 50 nm-thick poly(methylmethacrylate) (PMMA) layer were excited at 635 nm with a 250 W Tungsten continuous-wave light source, resulting in an effective excitation power of 1.6 mW cm\\u22122.\\n\\nMacroscopic KP measurements were performed under ambient conditions using a 2 mm diameter gold tip amplifier (Ambient Kelvin Probe Package from KP Technology Ltd). The KP technique provided a voltage resolution of about 5 mV on a sampled surface area of about 3 mm2. A comprehensive description of the technique can be found elsewhere.\\n\\nThe sheet resistance of WO3\\u2212x films on glass was performed in air and at RT conditions using an Ecopia 3100 system in the van der Paw configuration where gold tips were placed on the four corners of squared samples.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: WO3,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"20 mL of hydroiodic acid (57 wt% in H2O) was added dropwise to 48 mL methanol (40 wt%) under ice bath stirring for 2 h. The reactant solution was distilled in a rotary evaporator at 55 \\u00b0C to remove the solvents, and then the precipitate was washed by diethyl ether 3 times. Finally, a white-colored powder was collected and dried at 60 \\u00b0C for 24 h under vacuum. The mixture of PbCl2:CH3NH3I with a 1:3 molar ratio was dissolved in DMF and then stirred at 60 \\u00b0C overnight, giving the perovskite precursor solution.\\n\\nThe used device structure is shown in Fig. 1(a). ITO-coated glass substrates (15 \\u03a9 sq\\u22121) were ultrasonically-coated in acetone and ethanol at room temperature for 15 min, then UV-Ozone cleaner for 15 min. A film (45 nm thick) of PEDOT:PSS was spin-coated onto the ITO substrate at 4500 rpm and annealed at 140 \\u00b0C for 10 min. Then, the prepared perovskite precursor solution was spin-coated at 4000 rpm. For the thermal annealing process, the perovskite films were conducted by a typical gradient increased temperature method (the films were slowly heated from 60 to 100 \\u00b0C at a rate of 10 \\u00b0C/10 min on a hot plate). For the EEF assisted annealing process, EEFs were exerted on the perovskite films using a conductive glass cover, where a spacing of about 60\\u201380 \\u03bcm was set [Fig. S1(a)\\u2020]. To acquire the spacing, we put a plastic strip between two of the same conductive substrates to build a similar flat capacitor with air as the dielectric. Using C = \\u03b5A/d, the spacing can be deduced by measuring the capacitance. The electric field intensity (E) can be obtained based on E = V/d, where V is the applied DC voltage (60 V or 150 V). During the cooling process from 100 \\u00b0C to room temperature, the EEF was kept constant, and the photo taken during the EEF assisted annealing treatment is shown in Fig. S1(b).\\u2020 A PCBM layer was deposited from a 20 mg mL\\u22121 chlorobenzene solution at 2000 rpm. Then 0.5 mg mL\\u22121 Bphen in absolute ethanol was coated onto a PCBM layer at 4000 rpm. Finally, 100 nm thick Ag (mask area of 0.0725 cm2) was deposited on top of the Bphen layer by thermal evaporation under 10\\u22127 Torr.\\n\\nJ\\u2013V characteristics of the PSCs were recorded under 1 sun illumination using a programmable Keithley 2400 source meter under AM 1.5G simulated solar light. Incident photon current efficiency (IPCE) was measured by a 1000 W halogen lamp and grating monochromator (Acton Spectra Pro 2300i). Electrical impedance spectroscopy (EIS) and Mott\\u2013Schottky capacitance analysis were surveyed by Ivium (Netherlands). The absorption spectra were measured with a UV/vis spectrophotometer (PerkinElmer Lambda 750). The surface morphology and element distribution in energy dispersive X-ray (EDX) were characterized by scanning electron microscopy (SEM, Quanta 200 FEG, FEI Co.). X-ray diffraction (XRD) patterns were measured using PANalytica 80 equipment (Empyrean, Cu K\\u03b1 radiation with a wavelength of 0.154 nm). 2D-GIXRD patterns were obtained by a MarCCD 225 detector mounted vertically at a distance of around 256.401 mm from the sample with an exposure time of 100 s at a grazing incidence angle of 0.2\\u00b0. The coordinates of the GIXRD patterns were represented by diffraction vectors with q = 4\\u03c0sin(\\u03b8)/\\u03bb, where \\u03b8 is half of the diffraction angle and \\u03bb is the wavelength of the incident X-ray. P\\u2013E loops were tested by PMF0312-295 (Radiant Technologies, USA). The dielectric spectra were tested by a Precision Impedance Analyzer (Agilent 4294A).\\nKelvin Probe Force Microscopy (KPFM) is tested by PMF0312-295 (Radiant Technologies, USA), which is based on Atomic Force Microscopy (AFM) (Fig. S7(g) in the ESI\\u2020). Firstly, the surface topography is mapped in the tapping mode. Secondly, the contact potential difference (CPD) between the AFM tip and the sample is detected by retracing at a left height from the sample surface. During the second test procedure, a compensated DC voltage is applied to offset the potential difference between the tip and sample. Therefore, local potential distribution on the sample surface is observed, and the work function of the sample is obtained if the tip\\u2019s work function is known. All measurements are taken in air conditions.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Bphen,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylamine solution (40 wt% in ethanol), hydriodic acid (57 wt% in H2O) and lead(II) iodide (PbI2, 99.999%) were purchased from Alfa or Sigma-Aldrich. Phenyl-C61-butyric acid methyl ester (PCBM) was obtained from Solarmer Materials Inc. Methylammonium iodide (MAI) was synthesized according to the literature by stoichiometrically reacting methylamine with hydriodic acid. The perovskite precursor was prepared by mixing MAI and PbI2 in a molar ratio of 1:1 in anhydrous N,N-dimethylformamide (DMF, 99.8%, Alfa), and the final concentration of the perovskite was controlled to approximately 40 wt%. The solution was stirred overnight at room temperature and filtered with 0.45 \\u03bcm PVDF filters before spin-coating. The synthesis and characterization of PDINO were reported elsewhere.\\nFirst, the patterned ITO substrates were sequentially ultrasonically cleaned with detergent, deionized water, acetone and isopropanol. On the cleaned ITO substrate, the PEDOT:PSS aqueous solution filtered through 0.45 \\u03bcm PVDF filters was spin-coated at 4000 rpm for 30 s and then dried at room-temperature in air. The as-prepared perovskite precursor solution was spin coated onto the ITO/PEDOT:PSS substrate at a speed of 5000 rpm for 30 s. During the last 4.5 s of the spinning process, chlorobenzene was quickly added to induce fast crystallization. Then the perovskite film was treated by air, TA or WVA methods under the following treatment conditions: (1) air treatment. The sample plates of the spin-coated perovskite films were placed at room temperature in air (25 \\u00b0C, RH% < 10%). (2) TA treatment. As a control, the TA process was conducted by putting the sample plates on a hot plate maintained at 100 \\u00b0C for 10 minutes in air (RH% < 10%). (3) WVA treatment. The sample plates of the spin-coated perovskite films were put in Petri dishes (with a cover but not sealed) with vapors of water with different volumes and different duration times. The treatment was performed at room temperature in air (25 \\u00b0C, RH% < 10%). After the WVA or TA treatments, the PCBM (20 mg mL\\u22121 in chlorobenzene) and PDINO (1 mg mL\\u22121 in methanol) were then sequentially deposited by spin coating at 1500 rpm for 30 s and 3000 rpm for 30 s, respectively. Finally, a 100 nm Al electrode was deposited on the PDINO layer under high vacuum by thermal evaporation.\\nThe current density\\u2013voltage (J\\u2013V) characteristics were measured on a computer \\u2013 controlled Keithley 2450 Source \\u2013 Measure Unit. An Oriel Sol3A Class AAA Solar Simulator (model, Newport 94023A) with a 450 W xenon lamp and an air mass (AM) 1.5 filter was used as the light source. The input bias voltage was scanned in forward (\\u22121.5 V to 1.5 V, FS) and reverse directions (1.5 V to \\u22121.5 V, RS) in 0.01 V steps with a scan rate of 0.1 V s\\u22121. The measurement was through a shadow mask with an active area of 0.05 cm2 under illumination at ca. 25.0 \\u00b0C. The light intensity was calibrated to 100 mW cm\\u22122 by using a Newport Oriel 91150V reference cell. The EQE spectra were recorded with an Enli Technology (Taiwan) EQE measurement system (QE-R), and the light intensity at each wavelength was calibrated with a standard single-crystal Si photovoltaic cell. The thickness of the interlayer was determined by using a Profilometer (Ambios Tech. XP-2). Scanning electron microscopy (SEM) was performed in order to investigate the morphology of the perovskite films prepared on top of PEDOT:PSS. Top-view and cross-sectional images were characterized by using a HITACHI s-4800 (Hitachi Limited, Japan) using an InLens detector operating at an accelerating voltage of 10 kV. The atomic force microscopy (AFM) images were obtained by utilizing a SPA-400 SPM (Seiko Instrument, Inc.). The X-ray diffraction (XRD) patterns were recorded on a D/MAX-2000 X-ray diffractometer with monochromated Cu K\\u03b1 irradiation (\\u03bb = 1.5418 \\u00c5). The time-resolved PL measurements at the peak emission of \\u223c765 nm were recorded by using a lifetime and steady state spectrometer (FLS980, Edinburgh Instruments Ltd.) with a 470 nm laser.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PDINO,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.05,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PBDTT-DPP polymer & PFN, PCBM and PC70BM were purchased from 1-Material Inc., Solarmer Materials Inc. and Nano-C, respectively. CH3NH3I was synthesized by following the reported procedure. PbCl2 (Aldrich) and CH3NH3I were mixed in DMF or the DMF/DMSO (0.8:0.2 in Volume) solution at a molar ratio of 1:3 with different weight percentages.\\n\\nITO coated glass slides were cleaned by ultra-sonication for 30 minutes in detergent water, de-ionized water, acetone and ethanol, sequentially. The ITO substrates were then subjected to UVO treatment for 25 minutes. The PEDOT:PSS layer were spin-coated onto the ITO substrates. For the single-junction planar PVSK solar cells, the precursor in mixed DMF/DMSO solvent (60 wt%) was spin-coated onto the PEDOT:PSS layer. As a reference, the precursor in DMF solvent (60 wt%) was also spin-coated onto a PEDOT:PSS layer. The obtained films were subjected to low-temperature (60 \\u00b0C) annealing under vacuum for 40 minutes in order to remove the solvent. Then, the sequential films were annealed at 80 \\u00b0C for one hour to transfer the PVSK layers with a thickness of 220 nm. Then, the 40 nm thick PCBM layer was deposited onto the PVSK layer as a n-type layer and a PFN film with a thickness of 1 nm was spin-coated as an interfacial layer. Finally, a 80 nm thick Ag was thermally deposited as the cathode. For single-junction organic solar cells, the PBDTT-DPP/PC70BM blended solution (1:2, 18 mg ml\\u22121 in 1,2-dichlorobenzene o-DCB) was spin-coated onto the PEDOT:PSS layer to form a 110 nm thick layer. Ca (20 nm)/Al (100 nm) were sequentially thermal-evaporated as the cathode. The area of the cells was 0.06 cm2 as defined by the mask.\\n\\nThe fabrication of the front sub-cell mainly followed the procedure for the preparation of the single-junction device until the Ag cathode was deposited. The only difference was the variation of the PVSK layer thickness for optimization of the tandem devices. Sequentially, the Ag or Al doped MoO3/MoO3 bi-layer was deposited as an ICL, where the co-evaporation technique was used for the doped-MoO3 layer deposition. The content of Al in MoO3\\u2013Al step layer was kept between 40 and 50 wt%. The PBDTT-DPP/PC70BM blended solution (1:2, 18 mg ml\\u22121 in 1,2-dichlorobenzene o-DCB) was spin-coated onto the PEDOT:PSS layer to form a 110 nm thick layer. Ca (20 nm)/Al (100 nm) were sequentially thermal-evaporated as the cathode. The area of the cells was 0.06 cm2 as defined by the mask.\\n\\nThe work functions of different layers were measured by a Kelvin probe. The morphology of the PVSK layers on ITO/PEDOT:PSS substrates were characterized by scanning electron microscopy (SEM, Hitachi S-4800). The refractive index (n and k values) of the layers in the device structure was measured using a VASE ellipsometer from J. A. Woollam Co., Inc. Current density\\u2013voltage (J\\u2013V) characteristics were obtained by using a Keithley 2635 source meter and Newport AM 1.5G solar simulator with irradiation intensity of 100 mW cm\\u22122. The thicknesses of the layers were measured by a Dekak Stylus Profiler.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | PFN,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60; 80,\\n Perovskite_deposition_thermal_annealing_time: 30.0; 60.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Glass/ITO and PET/ITO substrates were purchased from Advanced Electronic Technology Co., Ltd. Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), phenyl-C61-butyric acid methyl ester (PC61BM), and 4-tert-butylpyridine (tBP) were supplied by Xi\\u2019an Polymer Light Technology Corporation. CH3NH3I (MAI) and PbI2 were purchased from Kunshan Sunlaite New Energy Technology Co., Ltd. Other materials were purchased from Aladdin.\\n\\nInverted-planar p\\u2013i\\u2013n perovskite solar cells (PSCs) were fabricated on laser-patterned, indium tin oxide (ITO) coated glass (rigid) and PET (flexible) (10 \\u03a9 sq\\u22121) substrates, respectively. Both of them were sequentially cleaned by ultra-sonication with deionised water, acetone, ethyl alcohol, and isopropyl alcohol (IPA) for about 15 min and then dried at high-temperature with clean dry nitrogen. After cleaning, the substrates were treated with ultraviolet (UV) ozone for 20 min to enhance the surface wettability. For the proposed cryo-controlled quasi-congealing spin-coating, low temperature (\\u223c5 \\u00b0C) PEDOT:PSS aqueous solution (with small amounts of DMSO) was spin-coated on the clean substrate at 0 \\u00b0C at 5000 rpm for 30 s, and then annealed at 120 \\u00b0C for 1 h. Detailed illustrations and mechanism of this technique are clearly described in the following section. The moisture-resistant CH3NH3PbI3\\u00b7xtBP was produced by two-step spin-coating. Firstly, the PbI2 precursor (1.2 M, dissolved in DMF and stirred for 1 h at 70 \\u00b0C) with 40 \\u03bcL mL\\u22121 of tBP was spin-coated on the PEDOT:PSS substrate at 4500 rpm for 30 s and dried at 70 \\u00b0C for 15 min. After the formation of PbI2\\u00b7xtBP, CH3NH3I (12 mg mL\\u22121, dissolved in the IPA solvent) was continuously spin-coated at 4000 rpm for 30 s to form CH3NH3PbI3\\u00b7xtBP and annealed at 100 \\u00b0C for 1 h. For the electron-transport layer (ETL), PC61BM (20 mg mL\\u22121 in chlorobenzene) was spin-coated on top of the perovskite layer at 2000 rpm for 30 s and annealed at 80 \\u00b0C for 1 h. The fabrication was completed by thermal evaporation of Ag as an electrode with a thickness of approximately 100 nm and an effective area of 0.06 cm2. The whole fabrication could be performed well in a high humidity environment (RH > 40%), which shows that the use of a glove box is not necessary. The fabrication process is illustrated in Fig. S1 (ESI\\u2020).\\n\\nThe photocurrent density\\u2013voltage (J\\u2013V) characteristics of the cells were measured using a Keithley 2400-SCS source meter under AM 1.5 illumination with an intensity of 100 mW cm\\u22122. The crystal structures of PbI2 and MAPbI3 were analysed by X-ray diffraction (XRD, Thermo ARL-X\\u2019TRA, America) with Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5). Field-emission scanning electron microscopy (FESEM, Ultra55, ZEISS, Germany) and atomic force microscopy (AFM, XEI-100E) were employed to analyse the morphologies. The incident photon-to-current conversion efficiencies (IPCEs) of the cells were measured with a quantum-efficiency (QE)/IPCE test system (Solar Cell Scan100/Zolix). Electrochemical impedance spectroscopy (EIS) measurements were carried out using an electrochemical workstation (Zennium Pro, Germany). The steady-state and time-resolved photoluminescence (TRPL) spectra were measured by using a PG2000-Pro-EX spectrophotometer (Shanghai Ideaoptics Corporation) and a transient fluorescence spectrometer (FLS980, Edinburgh Instruments, EI), respectively. The contact properties were characterised using a contact-angle instrument (Kr\\u00fcss Optronic, Germany). The UV-visible (UV-vis) absorption was measured using a UV-vis spectrophotometer (Lambda 900, America).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: TBP,\\n Perovskite_deposition_solvents: DMF | IPA,\\n Perovskite_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70 | 100,\\n Perovskite_deposition_thermal_annealing_time: 15.0 | 60.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Cryo-controlled quasi-congealing spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The molybdenum oxide (MoOx, STREM, 99.95%) and silver (Ag, Kurt Leskar, 99.99%) films were thermally evaporated using a MBRAUN evaporator with evaporation rate of 0.5 \\u00c5 s\\u22121 and 0.25 \\u00c5 s\\u22121, respectively. The indium and tin oxide target (ITO target, Plasmaterial 99.99%) films were RF magnetron sputtered using a Moorfield Nanolab 60 sputtering system at 0.37 W cm\\u22122 and 2.06 W cm\\u22122 for the bottom and top layers.\\n\\nPilkington TEC15 TM (<15 \\u03a9 cm\\u22122) glass was first gently scrubbed with a concentrated solution of Hellmanex\\u00ae III (10% by volume) diluted in de-ionised water and rinsed with copious amounts of de-ionised water. Substrates were then submerged and sonicated in a 2% by volume Hellmanex solution diluted in de-ionised water (\\u223c18 m\\u03a9) at 80 \\u00b0C for 20 minutes. After this time, the substrates were removed and rinsed with more de-ionised water and placed into a bath of de-ionised water (only) and sonicated for a further 20 minutes at 80 \\u00b0C to remove any residual surfactant. After this the substrates were subsequently rinsed with copious amounts of de-ionised water, acetone, ethanol and isopropanol. The substrates were then blown dry with a nitrogen air knife and placed into an oxygen plasma cleaner for 15 minutes on full power to remove any residual carbon contaminants and make the surfaces more hydrophilic. Lastly samples were placed in UV\\u2013ozone chamber for 15 minutes to aid with improved wettability and film formation for the subsequent SnO2 layer. Substrate preparation was carried out in a validated class 1000 clean room.\\nSnO2 ETL layers were prepared by diluting (44592) Tin(IV) oxide, 15% in H2O colloidal dispersion procured from Alfa Aesar further in de-ionised water to the ratio 1:2.6 mL to give a final solution of 4.2 wt%. These were then deposited via spin coating immediately after UV\\u2013ozone treatment of the FTO was finished. We note that the increased wetting effects of UV\\u2013ozone on FTO films lasts no longer than 10 minutes, we found it imperative that films were spin coated before this time limit elapsed. 150 \\u03bcL of the final ETL solution was spin coated onto a 28 mm by 28 mm glass/FTO substrate at 2000 rpm/2000 rpm s\\u22121 for 30 s, we noted improved surface coverage by depositing the solution dynamically at 25 s. The substrates were then placed on a hotplate at 110 \\u00b0C for 10 minutes then a 5 minute ramp to 180 \\u00b0C for 1 hour to anneal the final films. We note that processing conditions in the laboratory are critical to good film formation, noting that a very dry room (<25% RH) coupled with a nitrogen flowed Laurel (Model: WS-650 Mz-23NPPB spin processor) spin coater contributed to rapid drying of the film, resulting in detrimental pin hole defects. Increased humidity of >30% RH and no nitrogen flowing in the spin coater resulted in more homogenous films. These conditions should be considered when trying to fabricate such a layer as the effects can be easily negated although are not obvious during manufacture procedure was carried out in nitrogen filled glove-box.\\nMAPI perovskite was prepared by dissolving 605 mg of lead iodide (PbI2) procured from TCI America and 199 mg of methylammonium iodide (MAI) procured from GreatCellSolar in 1 mL of 4:1 ratio of dimethylformamide:dimethyl sulfoxide. We noted that by dissolving the inorganic PbI2 at elevated temperatures >150 \\u00b0C resulted in better perovskite film formation with fewer pinholes as report in literature. The solution was then filtered using a 0.2 \\u03bcm PTFE filter and deposited on top of the SnO2via solution processed spin coating (125 \\u03bcL, 4000 rpm/2000 rpm s\\u22121 for 30 s). During the spin coating process, 200 \\u03bcL of ethyl acetate procured from Sigma Aldrich was deposited dynamically onto the spinning substrate 22 s before the end the second spin programme. Once the spin coating procedure had finished the films were transferred to a hotplate and annealed at 100 \\u00b0C for 1 hour. The entire perovskite procedure was carried out in nitrogen filled glove-box.\\nFor the hole transporting material (HTM), a spiro-OMeTAD solution (100 mg of spiro-OMeTAD, 36 \\u03bcL of 4-tert-butylpyridine (tBP), 20 \\u03bcL of a lithium-bis(tri-fluoromethanesulfonyl)imide (Li-TFSI) solution (516 mg Li-TFSI in 1 mL acetonitrile) and 8 \\u03bcL of a FK209 (300 mg in 1 mL of acetonitrile) in 996 \\u03bcL of chlorobenzene) was spin-coated dynamically at 4000 rpm, 4000 rpm s\\u22121 for 12 s on top of the annealed perovskite. Again, the preparation and deposition of the HTM was performed in a nitrogen filled glove-box. Finally, 70\\u201380 nm of Ag top electrode was thermally evaporated under high vacuum.\\n\\nThe morphology of films was studied using a JEOL-JSM-7800F field emission scanning electron microscope (5 kV acceleration voltage, a working distance of 10 mm and a magnification of \\u00d750000). The transmittance of the IAI films were scanned suing a PerkinElmer Lambda 750 UV/VIS/NIR Spectrometer. The sheet resistance of the IAI films were measured using a Jandel RM3000 four-point probe station. X-ray diffraction data were collected on a D8 Discover (Bruker) X-ray diffractometer operating at 40 kV and 40 mA. Scans were collected between 10 and 60 degree with a 0.02 degree step.\\nFor current\\u2013voltage measurements of solar cell devices were masked to 0.09 cm2 and tested under a class AAA solar simulator (Newport Oriel Sol3A) at AM 1.5 and 100 mW cm\\u22122 illumination conditions calibrated against a KG5 filtered silicon reference cell (Newport Oriel 91150-KG5) using a Keithley 2400 source meter. Current\\u2013voltage sweeps were performed from both VOC to JSC and vice versa at a rate of 0.1 V s\\u22121. For stabilized power output measurements, device bias was set to the maximum power point voltage determined by the J\\u2013V sweep and current monitored under 1000 W m\\u22122 illumination.\\nStability measurements were performed on unencapsulated devices kept at open circuit in a light soaking unit (Solaronix Solixon A20), at 25 \\u00b0C and ambient humidity, under 1 sun illumination: both reverse and forward scans, at 15 mV s\\u22121 scan rate, were carried at every hour. The time lapse photography and RGB analysis to assess the colour change of the different films and thus their degradation over time were carried out as in our previous work.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: FK209; Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All reagent grade chemicals were obtained commercially from Sigma-Aldrich, St Louis, MO, unless noted otherwise. MAI was prepared in-house. In a typical procedure, 24 ml of a 33 wt% methylamine (CH3NH2) solution in anhydrous ethanol was reacted with 10 ml of 57 wt% hydroiodic acid (HI) in water, in 100 ml of ethanol (excess CH3NH2) in a dry Ar atmosphere at room temperature. The solvent and excess CH3NH2 were removed using a rotary evaporator, and the resulting MAI powder was harvested.\\n\\nFirst, a 0.8 M PbI2 (Alfa-Aesar, Ward Hill, MA) solution in N,N\\u2032-dimethylformamide (DMF) was spin-coated onto different substrates: plain glass, quartz, previously patterned fluorine-doped tin oxide (FTO) coated glass (TEC15, Hartford Glass Co., Hartford City, IN), or the patterned FTO-coated glass with a TiO2 blocking layer (\\u223c15 nm). A smooth, nanoporous PbI2 thin film was formed, which was then dried at room temperature under blowing air. Second, a fresh MAI solution of 10 mg ml\\u22121 in anhydrous isopropanol was spin-coated onto the as-prepared PbI2 layer immediately, and was then annealed at 150 \\u00b0C for 1 min, which constitutes the first SSCA cycle. This SSCA cycle was then repeated 3 to 4 times. The excess MAI was washed with isopropanol, and the final thin films were annealed at 150 \\u00b0C for 2 min to obtain a dark-colored perovskite film. The film thickness can be controlled by the spinning conditions. The spin-coating conditions of 4000 rpm for 15 s was used for all thin film depositions, which resulted in 250\\u2013300 nm MAPbI3 perovskite thin films. The nature of the substrate (plain glass, quartz, FTO-coated glass, and FTO-coated glass with a TiO2 blocking layer) did not have any obvious effects on the SSCA-processed MAPbI3 perovskite films.\\n\\nFor the fabrication of the PSCs, the FTO-coated glass was patterned by 25% hydrochloric acid etching with zinc powder, and cleaned by soaking in a base bath (5 wt% NaOH in ethanol) overnight. After washing with deionized water and ethanol, a compact TiO2 blocking layer was deposited on top of the patterned FTO by spray pyrolysis at 450 \\u00b0C. The perovskite layer was then deposited using the SSCA process (one, two or three SSCA cycles), as described above. This was followed by spin-coating a solution of a HTM, which consisted of 80 mg 2,2\\u2032,7,7\\u2032-tetrakis(N,N-dip-methoxyphenylamine)-9,9\\u2032-spirobifluorene (Spiro-MeOTAD; Merck, Germany), 30 \\u03bcl bis(trifluoromethane) sulfonimide lithium salt stock solution (500 mg Li-TFSI in 1 ml acetonitrile), 30 \\u03bcl 4-tert-butylpyridine (TBP), and 1 ml chlorobenzene solvent. The HTM spin-coating process was performed in a dry-air atmosphere with less than 10% humidity. Finally a 150 nm Ag layer was deposited using a thermal evaporator and a shadow mask. The PSCs were stored in a dry-air atmosphere with a humidity below 5%, and the performance of the PSC was typically measured one day after their fabrication.\\n\\nX-ray diffraction (XRD) was performed on a X-ray diffractometer (D8-Advance, Bruker, Germany) using Cu K\\u03b11 radiation (\\u03bb = 1.5406 \\u00c5) at step size/time of 0.02\\u00b0/1 s. The surface morphology of the films was observed by scanning electron microscopy (SEM; LEO 1530VP, Carl Zeiss, Germany). The local roughness of the MAPbI3 thin films were characterized by atomic force microscopy (AFM; 5500, Agilent, Santa Clara, CA) operated in contact mode. Optical spectroscopy (transmission, refection, absorption) of the films on quartz at each formation stage was conducted on a spectral response measurement system (QEXL, PV Measurements, Boulder, CO). Transmission electron microscopy (TEM) was used to characterize cross-sections of the whole PSCs. Note that this particular PSC has a thinner HTM layer compared to most of the other PSCs fabricated in this study. The samples from specific locations on the cross-sections were prepared by focused ion beam (FIB; Helios 600, FEI, Hillisboro, OR) and in situ lift-out. The TEM specimens were examined by TEM (2100F, JEOL, Tokyo, Japan) operated at a 200 kV accelerating voltage.\\n\\nThe incident external quantum efficiency (EQE) spectra of the PSCs were recorded at a chopping frequency of 5 Hz in AC mode on a solar cell quantum efficiency measurement system (QEX10, PV Measurements, Boulder, CO). The current density (J)\\u2013voltage (V) characteristics of the PSCs were obtained using a 2400 SourceMeter (Keithley, Cleveland, OH) under simulated one-sun AM 1.5G illumination (100 mW cm\\u22122) (Oriel Sol3A Class AAA Solar Simulator, Newport Corporation, Irvine, CA). A typical J\\u2013V scan starts from a forward-bias to a short-circuit at a rate of 20 mV s\\u22121. A typical active area of 0.12 cm2 was defined using a non-reflective mask for the J\\u2013V measurements. The steady-state maximum power output of the solar cells was measured by monitoring the current density (J) output at the maximum power voltage (V) bias for up to 300 s using a VersaSTAT MC potentiostat (Princeton Applied Research, Acton, MA). The current output can be converted to a power conversion efficiency (PCE) output using the following equation: PCE = (J (mA cm\\u22122) \\u00d7 V (V))/(100 (mW cm\\u22122)). A shutter was used to switch on and off the one-sun illumination on the cell. Solar-cell testing was conducted in the ambient atmosphere with a humidity of 20\\u201340%. Impedance spectroscopy (IS) on the PSCs was performed using a PARSTAT 2273 workstation (Princeton Applied Research, Acton, MA) with the frequency range of 0.1 Hz\\u2013100 kHz and the modulation amplitude of 10 mV. The IS spectra were analyzed using ZView 2.9c software (Scribner Associates, Southern Pines, NC).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spray-pyrolys,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 150 >> 150,\\n Perovskite_deposition_thermal_annealing_time: 1.0 >> 2.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.12,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The solar cells have been prepared following a recently described method. In brief MAPbI3 was prepared by a two-step spin coating procedure. The PbI2 layer was first deposited on the mesoporous TiO2 film deposited fluorine-doped tin oxide (FTO) conductive glass, which was followed by coating the MAI solution. The MAPbI3 layer was finally annealed at 100 \\u00b0C for 5 min. Spiro-MeOTAD was spin-coated on the MAPbI3 layer and Au was finally deposited on the spiro-MeOTAD. Incomplete cells with three different MAI concentrations (0.032 M, 0.044 M and 0.063 M) without HTL and Au electrode were also analysed. The preparation procedures were kept identical to the complete devices.\\n\\nThe solar simulator used is equipped with a 1000 W xenon short arc lamp and a Keithley 2651A source meter. The light intensity was calibrated through a Si reference cell in order to give a 1 sun light intensity according to the AM 1.5 G spectrum (class A, AM 1.5 G deviation <2%). No spectral mismatch correction was applied. For efficiency measurements, the cells were equipped with a non-reflective black mask which defined a 0.16 cm2 active area (out of the total active area size of \\u223c0.5 cm2). The scan direction was from the starting voltage of 1.2 V towards the final point at \\u22120.1 V with a 20 mV voltage step and 200 ms time interval between each step. For each typology 3\\u20135 cells were measured giving average conversion efficiency and standard deviation of 7.87 \\u00b1 1.31%, 17.07 \\u00b1 0.31%, 12.03 \\u00b1 0.58% for 0.032 M, 0.044 M and 0.063 M, respectively. The largest standard deviation for 0.032 M devices is also representative for the stronger non-uniformity of the perovskite layer. Out of the 3\\u20135 samples for every cell typology, one device was chosen for the complete characterization (I\\u2013V sun, I\\u2013V dark, VOCvs. light intensity, EL- and PL-imaging and \\u03bc-LBIC) and the corresponding results shown.\\n\\nThe investigation of surface and cross sections of the TiO2/perovskite films was carried out through a Schottky emission scanning electron microscope SEM (Hitachi, SU-70).\\n\\nThe experimental PL setup consists of a cooled 1 MP Silicon CCD camera, a spatially homogeneous excitation light in the whole active area of the cell (\\u223c0.5 cm2) with about 1.2 Sun light intensity obtained by a 2 halogen-lamp-system filtered by a 650 nm dielectric short-pass filter and an absorption band-pass filter with a transmittance of 500\\u2013900 nm. A power source and a stack of optical filters between the camera and the sample completed the equipment. The filter stack of the camera lens was composed of a 725 nm dielectric long-pass and an absorption long-pass with a smooth edge from 720 nm to 760 nm in order to obtain a sufficient suppression of excitation light incident on the camera. Furthermore a short pass filter is put in front of the camera filter stack to suppress light above 900 nm. The operating point of the cell was changed through the power source from VOC to 0 V. PL images were acquired with 50\\u2013100 mV voltage steps (smaller voltage steps close to VOC were used to better follow the steep I\\u2013V curve behaviour in this range). For every step an equilibration time of 2 s was used. Integration time was in the range 0.1\\u20130.5 s per image. The spatial resolution was about 40 \\u03bcm per camera pixel. The EL setup shared the same equipment. EL measurements were performed in the dark by application of a forward bias voltage. The filter stack was removed since no filtering of excitation light was necessary. The operating point of the cell was changed from 800 mV to 1300 mV with 50 mV voltage steps while EL images were acquired. Integration time was changed as a function of the operating point from 60 s to 0.5 s in order to get a high signal-to-noise ratio. It was observed that the prolonged application of high voltages during EL measurements reversibly modified the electrical characteristics of the cell. In particular, the current at a fixed high voltage was seen to decrease. A similar behaviour was also observed on the PL intensity (decrease) with light exposure. Following equilibrium conditions, the original parameters were restored within tens of seconds. A short integration time was used for PL and EL in order to minimize the device perturbation. Moreover, a recovery time of 60 s was taken between every step to avoid overheating of the device (in case of PL) and permit a complete device re-equilibration.\\n\\n\\u03bc-PL and \\u03bc-LBIC (Light Beam Induced Current) allow the investigation of photoluminescence and current generation with a micrometric resolution on the device. The cell is mounted on a movable stage. Excitation is done via a frequency doubled Nd:YAG laser at 532 nm, which is focused on the sample. For the large area \\u03bc-LBIC maps, an objective lens with an NA = 0.26 is used to obtain a low depth of focus. The intensity is set to 1 sun equivalent photon flux of about 7 \\u00d7 1017 cm\\u22123 s\\u22121 and spot size to 20 \\u03bcm in diameter. The induced current is measured by a highly sensitive current preamplifier. Emitted PL is collected with the same lens as is used for excitation, directed towards a grating spectrometer and detected by a silicon line CCD. By so doing the PL spectrum can be detected in the illuminated spot. By raster scanning the sample, the spatial resolution is established which is diffraction limited. For the highly resolved \\u03bc-PL maps an objective lens with numerical aperture of NA = 0.9 is used, which allows for a diffraction limited spot size of 260 nm and a corresponding spatial resolution. Typical integration times are 10 ms\\u2013100 ms per pixel. In complete devices the laser beam was shone from the glass side, meaning that the light passes through the TCO glass till the Au back electrode of the cell. In the case of properties\\u2019 investigation of perovskite crystals, incomplete cells were used (TCO/compact_TiO2/mesoporous_TiO2/perovskite). The high resolution \\u03bc-PL images were carried out with laser excitation from the perovskite crystal side (capping layer side). 3\\u20135 cells for each typology were tested for generating enough statistical data for a robust investigation of \\u03bc-PL/\\u03bc-LBIC. The resulting differences among samples of similar typology were very small compared to the differences between devices with different MAI concentrations. The cells were stored under dark and in a humidity-free environment throughout the PL\\u2013EL measurement timespan to prevent degradation effects.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: ,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> 5.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: Li-TFSI; TBP,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.16,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"For the perovskite layer, the MAPbI3 solution was composed of methylammonium lead trihalide (CH3NH3I) and lead(II) iodide (PbI2) in a ratio of 1.06:1 mol%, and it was mixed in gamma-butyrolactone (GBL) and DMSO (7:3 v/v%) with a molar concentration of 1.4 mol L\\u22121 at 100 \\u00b0C for 4 h. The Clevios P VP AI 4083 type of PEDOT:PSS was purchased from Heraeus (Germany). The PC70BM solution was dissolved in chlorobenzene (CB) in a concentration of 20 mg mL\\u22121.\\n\\nBoth CON-10 and CON-16 suspensions were prepared by dissolving 4 mg of each CON in 1 mL of DMSO with ultrasonication for 30 min.\\n\\nThe inverted perovskite photovoltaic devices were fabricated on a structure consisting of ITO/(CON)/PEDOT:PSS/MAPbI3/PC70BM/(TiOx)/Al. To fabricate the inverted PSC devices, patterned ITO glasses were washed via 20 min sonication in deionized water, acetone, and 2-propanol. After cleaning, the ITO glasses were dried at 100 \\u00b0C and then treated with ultraviolet (UV) ozone for 15 min. The CON solutions were spin-coated onto ITO glasses at 2000 rpm for 40 s and then annealed at 100 \\u00b0C for 5 min. Prior to the PEDOT:PSS coating onto the CON films, the CON films were treated with UV ozone for 5 min. The PEDOT:PSS was then spin-coated onto the ITO substrates or the CON films at 5000 rpm for 40 s. The PEDOT:PSS films were annealed on a hot plate at 140 \\u00b0C for 10 min to generate a thin film with a thickness of 30 nm. The MAPbI3 solution was first spin-coated on a PEDOT:PSS film at 1000 rpm for 30 s and then again at 5000 rpm for 30 s with an additional process of CB drop-casting. Then, the substrates were placed on a hot plate at 100 \\u00b0C for 5 min to fabricate the MAPbI3 film with a thickness of 300 nm. A PC70BM layer with a thickness of \\u223c30 nm was formed on the perovskite layer at 2000 rpm for 40 s. A TiOx interlayer with a thickness of \\u223c10 nm was subsequently added on the active layer at 5000 rpm for 40 s. Finally, an Al cathode was thermally deposited under 4.0 \\u00d7 10\\u22126 Torr with a thickness of \\u223c100 nm using a thermal evaporator. All the devices were encapsulated using a UV-curable resin and a cover glass.\\n\\nThe surface morphologies and roughness of the hole transport and perovskite layers were characterized using the Park NX10 AFM device (Park Systems, South Korea) in the noncontact mode and the SIGMA SEM (Carl Zeiss, Inc., USA) instrument at 5 kV, respectively. In addition, the Bruker-AXS XRD device (Bruker, South Korea) was used to investigate the crystallinity of the perovskite thin films.\\n\\nThe J\\u2013V characteristics of the fabricated inverted OPVs were assessed using the ZIVE SP1 instrument (ZIVE LAB, South Korea) under an AM 1.5-G solar simulator (light and dark conditions). The SCLC and Jph values were measured under the AM 1.5-G solar simulator and the dark condition, respectively. The total cell area of the fabricated inverted PSCs was 0.15 cm2. The IPCE values were measured to prove the short-circuit current of the Jsc. The PL spectra were obtained using the XPERAM 200 Raman microscope (Nanobase, Inc., South Korea). The laser wavelength and the power for each device were 642 nm and 0.3 mW, respectively.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | TiO2,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Unknown,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"For band gap calculations, we firstly obtained the film absorption spectra with a Hitachi U-3010 spectrophotometer in diffusion reflectance mode. Then, the Tauc plot was used to derive band gap values. Since perovskites have direct allowed transitions, we used the following equations for calculation:\\nwhere \\u03b1 is the absorption coefficient, which is derived from the absorption spectra; h is Planck's constant, \\u03bd is the light frequency, and Eg is the band gap. The Tauc plot has a distinct linear regime which denotes the onset of absorption. Then extrapolating this linear region to the abscissa yields the optical band gap.\\n\\nThe clean FTO glasses were used as the substrate for NiMgLiO deposition. The precursor for NiMgLiO was prepared according to the previous reference. In brief, 822.1 mg nickel acetylacetonate, 128.4 mg magnesium acetate tetrahydrate, and 13.2 mg lithium acetate were dissolved in 200 mL of acetonitrile/ethanol (volume ratio of 95:5) solutions. The film was fabricated by spray coating with FTO as the substrate at 500 \\u00b0C. 30 mL of the above solutions was sprayed using a home-made spray device, with one cycle for 5 seconds (2 seconds for spray, 3 seconds for waiting) and 70 cycles in total. After another 20 min annealing at 500 \\u00b0C in air, the NiO film was fabricated.\\nMAPbI3 perovskite films were fabricated through the following method. Firstly, the precursor solution was prepared by dissolving PbI2 and MAI in a mixed solvent (\\u03b3-butyrolactone:DMSO = 7:3 vol%), with the concentration set to 0.96 M. Then the solutions were coated onto the NiMgLiO film by two consecutive spin-coating steps, at 1500 rpm for 10 s and 5000 rpm for 30 s. During the second step, 0.3 mL chlorobenzene was poured onto the substrate. Then the film was annealed at 90 \\u00b0C for 10 min. Cs0.05FA0.15MA0.8PbI3 films were fabricated using a mixture of CsI, FAI, MAI, and PbI2 in an ideal ratio as the mixed solvent. The concentration was optimized to be 1.2 M. Then the films were annealed at 90 \\u00b0C for 10 min.\\nThen 15 mg mL\\u22121 chlorobenzene solution of PCBM was spin-coated onto the perovskite at 1500 rpm for 30 s, followed by spin-coating of isopropanol solution with saturated BCP at 1500 rpm for 30 s. Finally, a 120 nm Ag electrode was thermally evaporated on top of the device under high vacuum (<10\\u22124 Pa). The active area of the device was 0.16 cm2 with a mask of 0.09 cm2.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: Cs0.05FA0.15MA0.8PbI3,\\n Perovskite_composition_short_form: CsFAMAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiMgLiO,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spray-pyrolys,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless stated otherwise, all materials were purchased from Sigma-Aldrich and used as received. Poly(bis(4-phenyl)(2,4,6-trimethylphenyl)amine) (PTAA) was purchased from Xi'an Polymer Light Technology Corporation. Poly(3,4-ethylenedioxy-thiophene):poly(styrenesulfonate) (PEDOT:PSS) (Clevios P VP Al 4083) was purchased from H. C. Stark Company. CH3NH3I (MAI) and CH(NH2)2I (FAI) were purchased from Shanghai Materwin New Materials Co. Ltd. SnI2 (99.999%) was purchased from Alfa Aesar. PC61BM was purchased from American Dyes Source, Inc. ZnO nanoparticles were synthesized via a sol\\u2013gel process using Zn acetate and tetramethylammonium hydroxide ethanol (TMAH). TMAH\\u00b75H2O (543.24 mg) dissolved in ethanol (5.45 mL) was added dropwise to Zn(Ac)2\\u00b72H2O (657.33 mg) dissolved in DMSO solvent, followed by stirring for an hour at room temperature. After washing at least two times in ethanol, ZnO nanoparticles were dispersed in pure isopropanol at a concentration of \\u223c10 mg mL\\u22121. The ITO substrate was purchased from Hangzhou Hongshi Electronic Technology Co., Ltd, and its resistance is 8\\u201310 \\u03a9 per \\u03b3.\\n\\nThe one-step FA0.7MA0.3Sn0.3Pb0.7I3 precursor solution (1 M) was obtained via mixing stoichiometric amounts of FAPbI3 (1 M) and MASnI3 (1 M) precursors into a DMF and DMSO mixed solvent (molar ratio of 1:1) and stirring at 70 \\u00b0C for 2 h. The two-step Sn0.3Pb0.7I2 precursor solution (1 M) was prepared via dissolving SnI2 (111.75 mg) and PbI2 (322.70 mg) into 1 mL of DMF and 71 \\u03bcL of DMSO and stirring at 70 \\u00b0C for 2 h. The FA0.7MA0.3I precursor solution (1 M) was prepared via dissolving FAI (39.39 mg) and MAI (15.61 mg) into 1 mL of isopropanol. PC61BM was dissolved in chlorobenzene at a concentration of 20 mg mL\\u22121. PTAA was dissolved in toluene at a concentration of 5 mg mL\\u22121.\\n\\nThe ITO-coated glass substrates were cleaned via sonication using detergent, deionized water, acetone, and isopropanol sequentially for 20 min each, followed by 20 min of ultraviolet ozone (UV-ozone) treatment. Then a layer of 30 nm thick PEDOT:PSS was spin-coated onto the cleaned ITO at 4000 rpm for 40 s, and baked in air at 140 \\u00b0C for 15 min. The substrates were transferred into a glovebox (the O2 and H2O concentrations were kept below 0.01 and 0.02 ppm). A layer of 10\\u201315 nm thick PTAA can be formed via spin-coating at 6000 rpm for 45 s in the glovebox. The one-step perovskite films were fabricated via spin-coating 30 \\u03bcL of precursor solution at 5000 rpm for 45 s and quickly dripping 150 \\u03bcL of chlorobenzene on this 6 s after the beginning. The films were placed on a hotplate at 120 \\u00b0C for 4 min. The two-step mixed precursor solution was spun on the PEDOT:PSS or PTAA layer at 3000 rpm for 30 s. Then, the mixed FAI and MAI solution was spun on the substrate at 3000 rpm for 30 s. Afterward, the obtained films were annealed at 130 \\u00b0C or 160 \\u00b0C for 10 min. A layer of 40 nm thick PC61BM was spin-coated at 2000 rpm for 30 s. A 40 nm thick hole-blocking layer was deposited via spin-coating ZnO nanoparticles at 4000 rpm for 30 s on top of the PC61BM layer. Subsequently, samples were loaded into a vacuum deposition chamber (background pressure \\u2248 5 \\u00d7 10\\u22124 Pa) to deposit a 100 nm thick Al cathode with a shadow mask, defining an active device area of 6.0 mm2.\\n\\nThe J\\u2013V characteristics were measured in a glovebox under 100 mW cm\\u22122 AM1.5G solar irradiation, and the steady-state photocurrents were measured at a bias voltage (0.58 V) near the maximum power point and at a stabilized power output for a period of 300 s. EQE spectra were measured using a Stanford Research System Model SR830 lock-in amplifier unit coupled with a monochromator and a 500 W xenon lamp, and a calibrated Si photodiode with a known spectral response was used as a reference. X-ray diffraction (XRD) patterns were recorded at a scan rate of 5 deg min\\u22121 using a Rigaku D/max-2550PC X-ray diffractometer with Cu K\\u03b1 radiation (1.5406 nm). The film morphologies were characterized using SEM (Quanta 400). UV-vis absorption spectra were obtained with a UV-vis spectrometer (Cary-5000). Steady-state PL spectra were obtained with an FLS920 fluorescence spectrometer at an excitation wavelength of 400 nm.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.7MA0.3Pb0.7Sn0.3I3,\\n Perovskite_composition_short_form: FAMAPbSnI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 4,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Patterned FTO glass with a sheet resistance of 15 \\u03a9 sq\\u22121 was purchased from Wuhan Geao (China). PEDOT:PSS with brand Clevious P VP AI 4083 was purchased from H. C. Stark. Methylamine solution (33 wt% in absolute ethanol), hydriodic acid (57 wt% in water) and isopropanol (99.8%, extra dry) were purchased from Acros Organics. N,N-Dimethylformamide (DMF) and lead(II) iodide (99.999%) were purchased from Alfa Aesar. PCBM was purchased from Solarmer Energy, Inc. All these commercially available materials were used as received without further purification.\\n\\nCH3NH3I was synthesized according to the previous literature with some modification. Typically, 34 mL of methylamine (33 wt% in absolute ethanol) and 38 mL of hydroiodic acid (57 wt% in water) were mixed in a 150 mL three-necked flask, and then stirred at 0 \\u00b0C for 2 h in an ice-water bath. After that, the mixtures were rotary evaporated at 50 \\u00b0C for 1 h to remove the solvent and white CH3NH3I precipitates were recovered. Finally, the product was washed with diethyl ether three times and dried at 60 \\u00b0C overnight in a vacuum oven.\\n\\nThe patterned FTO was sequentially ultrasonic cleaned twice with detergent, pure water, deionized water, acetone and isopropyl alcohol. The pre-cleaned substrate was ultraviolet ozone treated for 10 min. After that, the filtered PEDOT:PSS aqueous solution was spin-coated onto the pre-treated FTO-glass substrates at 3000 rpm for 35 s and then dried at 150 \\u00b0C for 15 min. A 350 mg mL\\u22121 PbI2 DMF solution was spin-coated on the FTO/PEDOT:PSS substrate and then annealed at 100 \\u00b0C for 10 min. The CH3NH3I thin layer was deposited by spin-coating 40 mg mL\\u22121 CH3NH3I isopropyl solution at 1000\\u20133000 rpm for 20 s and then annealed at 80 \\u00b0C for 5 min. The PbI2 film and CH3NH3I film were pressed together face to face with a 0.2, 0.4, and 0.6 mm hollow aluminum foil gasket between them, and the space is sufficient for the thickness increase of the PbI2 film when it grows into a CH3NH3PbI3 crystal. The whole sets were then annealed at 150 \\u00b0C in a vacuum oven under a pressure of \\u22120.1 MPa or non-vacuum oven, and the perovskite film was obtained on the PbI2 side. The process of simplified CSS to fabricate perovskite is shown in Fig. 1. After that, PCBM solution (30 mg mL\\u22121 in chlorobenzene) was spin-coated on the perovskite layer at 3000 rpm for 30 s. Finally, a 100 nm Al cathode was deposited through thermal evaporation under a pressure of 5 \\u00d7 10\\u22125 Pa.\\n\\nThe current density\\u2013voltage curves were measured under AM 1.5G illumination (100 mW cm\\u22122) using a solar simulator (SAN-EI, AAA grade) with a Keithley 2400 Source Meter under an N2 atmosphere. The light intensity was calibrated with a Si solar cell for 1 sun. The external quantum efficiency (EQE) was measured using QE-R systems (Enli Tech.). The light intensity at each wavelength was adjusted with a standard single-crystal Si photovoltaic cell.\\n\\nThe thickness of the films was recorded using a DektakXT profilometer (Bruker Nano, Inc.). The surface morphologies of the thin films were examined using an AC Mode III (Agilent5500) atomic force microscope (AFM) operated in the tapping mode under ambient atmosphere. The surface and cross-section morphologies of the thin films were further characterized using a Scanning Electron Microscope (SEM; HITACHI SU8010, Japan) operated at an accelerating voltage of 5.0 kV and 30 kV, respectively. The crystallinity of the perovskite films were measured using an X-ray diffractometer (Rigaku miniflex 600) in the 2\\u03b8 range of 5\\u201390\\u00b0 at a scanning rate of 5\\u00b0 min\\u22121. The optical absorption of the films was measured using a Shimadzu UV-2450 UV-visible spectrophotometer.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA >> none,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating >> Close space sublimation,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown >> Unknown >> 150.0,\\n Perovskite_deposition_thermal_annealing_time: Unknown >> Unknown >> 60.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I was synthesized by a method reported in the literature. PbI2 (99.99%), poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) (PEDOT:PSS), [6,6]-phenylC61-butyric acid methyl ester (PC61BM), and bathophenanthroline (Bphen) were purchased from Xi'an Polymer Light Technology Corp. N,N-dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), tetrahydrofuran (THF), chlorobenzene (CB), ethanol, and isopropanol were purchased from Sigma. Tetraphenyldibenzoperiflanthene (DBP) was bought from Taiwan Nichem Co., Ltd.\\n\\nThe DBP precursor solution was prepared by dissolving 10 mg DBP in 2 ml THF or CB. After filtration, it was diluted to 1, 2, 3, and 4 mg ml\\u22121, respectively. The perovskite precursor solution was prepared by dissolving 0.3482 g of MAI and 0.922 g PbI2 (MAI:PbI2 = 1.095:1) into 0.9 ml of DMF and 0.1 ml of DMSO mixed solvent. PCBM precursor solution was formulated to 20 mg ml\\u22121 in CB and the formula for the Bphen precursor solution was 0.7 mg ml\\u22121 in ethyl alcohol.\\nFirst, the patterned indium tin oxide (ITO) transparent conductive glass was ultrasonically and subsequently cleaned with deionized water, acetone, and isopropanol for 15 min, respectively. Then, the ITO glass was dried with nitrogen and placed in a plasma cleaner for 5 min before use. After that, 15 \\u03bcl of PEDOT:PSS was spin-coated on the cleaned ITO at 6000 rpm for 30 s. Then, the films were annealed at 120 \\u00b0C on a hotplate for 15 min in the air. Subsequently, the sample was sent to the glovebox and the perovskite precursor solution was spin-coated on the PEDOT:PSS/ITO substrate at 6000 rpm for 30 s. During the spin-coating process, sec-butanol (250 \\u03bcl) as an anti-solvent was dropped on the wet CH3NH3PbI3 precursor film at the 8\\u201310th s after spin-coating started. Then, the resulting film was annealed at 100 \\u00b0C for 30 s. The above spin-coating process was carried out in a glovebox under a nitrogen atmosphere with a real-time humidity of about 1 ppm. Finally, the perovskite film was transferred to a hot plate, first annealed in ambient air (at 100 \\u00b0C for 30 min, real-time humidity of 30\\u201350%), and then annealed in a DMSO atmosphere at the same temperature and time. For the DMSO atmosphere, 50 \\u03bcl of DMSO was dropped into a glass Petri dish, and then the sample was covered with a glass Petri dish. Subsequently, 25 \\u03bcl DBP precursor solution was spin-coated on the perovskite layer at 4000 rpm for 30 s and 25 \\u03bcl PC61BM precursor solution (20 mg ml\\u22121 in chlorobenzene) was spin-coated at 3000 rpm for 30 s. Then, the Bphen interfacial layer with a concentration of 0.7 mg ml\\u22121 in ethanol was spin-coated at 6000 rpm for 30 s without additional annealing. The device was completed by evaporating a 100 nm thick Ag film as an electrode. The active device area was set to 0.04 cm2 by the overlap region between the top Ag cathode and the bottom ITO anode.\\n\\nSEM images and XRD patterns of the films were obtained with a JSM-7100F from JEOL and a D/Max-B diffractometer from Rigaku, respectively. AFM and SKPM images were obtained using an atomic force microscope from a Park systems NX10 equipped with scanning Kelvin probe microscopy (SKPM). A solar simulator (ABET SUN3000) was used to provide simulated solar irradiation (AM 1.5G, 100 mW cm\\u22122). The J\\u2013V characteristics were measured using a Keithley 2400 source meter. The output of the light source was adjusted using a calibrated silicon photodiode (ABET technology). The J\\u2013V measured the curve by a forward scan from \\u22120.5 to 1.5 V and a reverse scan from 1.5 to \\u22120.5 V. EQE (Keithley 2400) was measured using a power source (ZOLIX CSC1011) with a monochromator and a source meter. The steady-state and the transient-state PL spectra were measured by a xenon lamp at 467 nm and a nanosecond-pulsed laser at 376.2 nm using a fluorescence spectrometer (FLS980, Edinburgh Instruments). The absorption spectra were recorded by a Shimadzu UV-2600. Contact angles were measured by XG-CAMA1.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | Bphen,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PSCs were fabricated with a regular n-i-p planar structure of ITO/SnO2/CsPbI2Br/poly-triarylamine (PTAA)/MoO3/Al. ITO-coated glass substrates (CSG Holding Co., Ltd, 10 ohm sq\\u22121) were cleaned stepwise with detergent, acetone, isopropanol and ethanol by sonication for 15 min each. After drying under a N2 stream, the substrates were treated with ultraviolet-ozone (UVO) for 15 min to generate a hydrophilic surface. The SnO2 colloid precursor (Alfa Aesar, 15 wt% in a H2O colloidal dispersion) was first diluted to 2.5 wt% with deionized (DI) water. Then, the diluted colloidal solution was spin-coated onto ITO substrates at 4000 rpm for 30 s, followed by annealing at 150 \\u00b0C for 30 min in ambient air. To avoid oxygen and moisture, the substrates were transferred into a nitrogen-filled glove box (<0.1 ppm O2 and H2O) for the rest of the device fabrication.\\nThe CsPbI2Br precursor solution was prepared by dissolving 208 mg of CsI (Sigma-Aldrich, 99.9%), 184 mg of PbI2 (TCI, 98%) and 148 mg of PbBr2 (Sigma-Aldrich, 99.999%) in 1 mL of DMF (Sigma-Aldrich, anhydrous, 99.8%) and DMSO (Sigma-Aldrich, anhydrous, 99.9%) (4:1, volume/volume), with stirring at 90 \\u00b0C for 2 h. The precursor solution kept at RT, was spin-coated on the ITO/SnO2 substrates heated at a certain temperature on a hot plate mounted on the spin-coater (hot-casting process; a photograph of the spin-coater is presented in Fig. S1, ESI\\u2020) or at RT (conventional RT-casting process) at 2500 rpm for 30 s. Right after spin-coating, the as-cast precursor film was annealed at a selected temperature for 10 min. A PTAA (Xi'an Polymer Light Technology Corp.) solution of 15 mg mL\\u22121 in chlorobenzene (Sigma-Aldrich, anhydrous, 99.8%) was then spin-coated on the perovskite at 3000 rpm for 30 s. Finally, 5 nm MoO3 and 100 nm Al were sequentially deposited by thermal evaporation at a base pressure of 9.0 \\u00d7 10\\u22125 Pa. The deposition rate and film thickness were monitored with a quartz crystal sensor. A shadow mask was put on the sample to define an active area of 4 mm2 before the metal deposition.\\n\\nThe current density\\u2013voltage (J\\u2013V) characteristics were measured using a Keithley 2400 source meter unit under simulated Air Mass 1.5 Global (AM 1.5 G) solar illumination at an intensity of 100 mW cm\\u22122, which was calibrated using a reference silicon solar cell. The measurements were carried out with the PSCs inside the glove box (<0.1 ppm O2 and H2O). The external quantum efficiency (EQE) spectra were measured using a QTEST HIFINITY 5 (Crowntech Inc., USA) at RT in air. The light intensity was calibrated using a single-crystal Si photovoltaic cell as a standard. X-ray diffraction (XRD) patterns were measured on a Rigaku-D/Max-3A X-ray diffractometer with monochromatic Cu K\\u03b1 irradiation (\\u03bb = 1.5406 \\u00c5). Scanning electron microscopy (SEM) analysis was performed on a Hitachi S-4800 electron microscope. Absorption spectra were acquired using a Shimadzu UV-2600 UV-vis spectrophotometer. Steady-state photoluminescence (PL) spectra were recorded on a Hitachi F-4600 fluorescence spectrophotometer.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: SnO2-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbBrI2,\\n Perovskite_composition_short_form: CsPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 340,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PTAA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The MASnxPb(1\\u2212x)I3 (MA = CH3NH3) perovskite precursor solution was formulated by dissolving a mixture of SnI2 (99.999%, Alfa Asear), PbI2 (99.999%, Alfa Aesar) and CH3NH3I (MAI, 99%, Xi'an Polymer Light Technology Corp.) in a molar ratio of x:(1 \\u2212 x):1.1 in a mixed solvent prepared using DMF (N,N-dimethylformamide, 99.5%, Aladdin) and DMSO (99.5%, Aladdin) at a volume ratio of 10:1. The MASnxPb(1\\u2212x)I3 thin films on the surface of the poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) substrate were formed by spin-coating the precursor solution at 6300 rpm, and after 5\\u201313 s of delay time the rotated wet films were washed with sec-butyl alcohol (99%, Aladdin) to promote fast nucleation and crystal growth. After the rotation stopped, the films were transferred onto a hot plate for annealing at 100 \\u00b0C for 25 s, followed by soaking in sec-butyl alcohol for 8\\u201310 s to remove excess MAI. Subsequently, the films were dried by spinning the substrates at 6300 rpm for 35 s. Finally, the films were thermally annealed at 100 \\u00b0C for 35 min under a N2 atmosphere and subsequently solvent annealed in a DMF atmosphere at 100 \\u00b0C for 35 min to assist the growth of crystalline domains. The film processes were conducted in a nitrogen-purged glove box with oxygen and moisture levels below 0.1 ppm. A schematic illustration of the fabrication steps of MASnxPb(1\\u2212x)I3 perovskite films is described in Fig. S1 in the ESI.\\u2020\\n\\nPerovskite solar cells have the structure of ITO/PEDOT:PSS/MASnxPb(1\\u2212x)I3/PC60BM/Al. Prior to the cell fabrication, the pre-patterned ITO-coated glass substrates were cleaned by ultrasonication sequentially with deionized water, acetone, and isopropanol for 20 min each. Next, the aqueous solution of PEDOT:PSS with a concentration of 1 mg ml\\u22121 (Heraeus) was spun onto ITO as a hole transport layer at 3000 rpm for 35 s in air, followed by annealing at 120 \\u00b0C for 10 min. Sequentially, MASnxPb(1\\u2212x)I3 perovskite films with a thickness of about 300 nm as an absorber were formed on the ITO/PEDOT:PSS substrate. Then, a chlorobenzene solution of [6,6]-phenyl-C60-butyric acid methyl ester (PC60BM, 99.5%, Solenne), with a concentration of 20 mg ml\\u22121, was spin-coated on top of the perovskite layer as an electron-transporting layer at 2000 rpm for 30 s. Finally, the device was obtained by thermal evaporation of an Al (150 nm) electrode.\\n\\nThe surface morphology of the films was analyzed using scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDS). The crystallinity of the perovskite films was examined by X-ray diffraction (XRD) measurements using a Rigaku D/Max-B X-ray diffractometer. The ultraviolet-visible (UV-vis) absorption spectra of the films were measured using an UV-Visible spectrometer with an integrating sphere (Shimadzu UV-2600). Current density\\u2013voltage (J\\u2013V) characteristics of all cells in the dark and under AM 1.5G illumination were measured using a programmable SourceMeter (Keithley 2400), with forward and backward scan rates of 0.08 V s\\u22121. The illumination was provided by a Sun 3000 Solar Simulator from ABET Technologies. The illumination power was corrected to 100 mW cm\\u22122 using a standard Si solar cell (certified by NREL). For the J\\u2013V measurement, a black mask with an aperture (0.16 cm2) was used to define the active area of the devices. The external quantum efficiency (EQE) as a function of wavelength was recorded using ZOLIX CSC1011 with a short arc xenon lamp source (Ushio UXL-553). The spot area of the incident beam is about 0.07 cm2. A Si photodetector model (certified by National Institute of Metrology, China) with known EQE was used to determine the spectral response of PSCs. All measurements were performed without encapsulation.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 0.5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.07,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS, Clevios P VP AI 4083) was provided by Heraeus. Copper(I) iodide (CuI, 99.999% trace metals basis), anhydrous acetonitrile (99.8%), anhydrous N,N-dimethylformamide (DMF, 99.8%), anhydrous 2-propanol (IPA, 99.5%), anhydrous chlorobenzene (CB, 99.8%), and anhydrous dimethyl sulfoxide (DMSO, 99.9%) were purchased from Sigma-Aldrich. Lead(II) iodide (PbI2, 99.9985%), methylammonium iodide (CH3NH3I; MAI), and formamidinium iodide (CH(NH2)2I; FAI) were purchased from Alfa Aesar and GreatCell Solar. [6,6]-Phenyl-C61-butyric acid methyl ester (PCBM) was purchased from Nano-C. Colloidal suspension of ZnO nanoparticles (Avantama N-10) was obtained from Avantama. All materials are commercially available and were used as received without further purification.\\n\\nThe p-i-n perovskite solar cells were fabricated with different combinations of ITO/hole transport layer (HTL): ITO/CuI, ITO/CuI/PEDOT:PSS and ITO/PEDOT:PSS/CuI. The device structure was ITO/HTL/perovskite/PCBM/ZnO NP/Ag. ITO-coated glass substrates were cleaned by sequential sonication in acetone and isopropyl alcohol (IPA) for 10 min each. N2 was blown to the glass/ITO substrates to complete the cleaning by removing IPA residues. Then oxygen plasma treatment was applied for 10 min. CuI solutions in acetonitrile with a concentration of 3 mg ml\\u22121 were prepared and stirred at room temperature for 3 h in a nitrogen filled glove box. CuI solutions were spin-coated on the cleaned ITO/glass substrates at 2000 rpm for 1 min. For some devices, CuI was spin-coated on top of PEDOT:PSS, or PEDOT:PSS was spin-coated on top of the CuI layer prior to the deposition of perovskites. As the surface of the CuI layer is hydrophobic, when PEDOT:PSS was spin-coated on top of CuI, a small amount of Dynol 604 (surfactant) was added to the PEDOT:PSS solutions to ensure good film coverage, and then the resulting solution was filtered through a 0.2 \\u03bcm PES filter. The filtered solutions were then spin-coated on the CuI-coated substrate at 3000 rpm for 1 min. All the following steps were performed in a glove box filled with nitrogen. PbI2 and MAI were dissolved (1.193 M for each) in a molar ratio of 1:1 in anhydrous DMF and the resultant mixture was stirred overnight at 70 \\u00b0C to produce the perovskite precursor solution. For the FAPbI3 precursor solution, FAI and PbI2 were dissolved (1 M for each) in a molar ratio of 1:1 in a mixed solvent with DMF and DMSO in a volume ratio of 4:1. The solutions were filtered with a 0.2 \\u03bcm PTFE filter before spin coating. The filtered perovskite precursor solutions were spin-coated at 5000 rpm for 55s on ITO/HTL substrates. During spin coating, 50 \\u03bcl anhydrous CB was dripped onto the substrate at 4\\u20135 s after spin coating started. After drying the perovskite films, MAPbI3 and FAPbI3 films were annealed on a hot plate at 100 \\u00b0C and 150 \\u00b0C for 20 min, respectively. Twenty milligrams of PCBM was dissolved in 1 ml anhydrous CB. To prepare the solution blends of PCBM and MAI, MAI was dissolved in anhydrous IPA at a concentration of 10 mg ml\\u22121. Then a small volume of the MAI solution was added into the PCBM solutions. Either PCBM solutions or PCBM:MAI solution blends were spin-coated at 2000 rpm for 1 min on top of the perovskite layer. Then, ZnO nanoparticles were spin-coated at 4000 rpm for 40 s. To complete device fabrication, Ag was thermally evaporated with a thickness of 100 nm in a vacuum chamber (\\u223c1 \\u00d7 10\\u22126Torr). The active area of the device is 5.25 mm2.\\n\\nThe current density\\u2013voltage (J\\u2013V) characteristics were recorded using a Keithely 2401 under 1 sun illumination (1000 Wm\\u22122 AM 1.5 G) from a solar simulator (Oriel Sol3A Class AAA Solar Simulators, Newport) using a xenon lamp. A standard silicon reference cell was used to calibrate the light intensity. Scans of J\\u2013V characteristics were performed with a forward (from short circuit to open circuit) and a reverse (from open circuit to short circuit) direction. The scan rate was 113 mV s\\u22121, unless indicated otherwise. To investigate the scan rate dependence, two different scan rates of 22.6 and 1130 mV s\\u22121 were considered. To age the devices, they were kept in the dark in the glove box before J\\u2013V characteristics measurements. The top view image of the CuI films prepared on ITO and PEDOT:PSS, and the cross-sectional image of the ITO/CuI/perovskite were acquired by scanning electron microscopy (SEM; JSM-7610F, JEOL) at an accelerating voltage of 5 kV. The optical absorption spectra of the perovskite films were collected with an Agilent 8453 UV\\u2013visible spectrophotometer. All the tested devices were unencapsulated.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 20,\\n HTL_stack_sequence: CuI,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0525,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Unless specified, all chemicals were purchased from Alfa Aesar or Sigma-Aldrich. Formamidinium iodide (FAI), methylammonium bromine (MABr), lead iodide (PbI2) and lead bromine (PbBr2) were purchased from Ying Kou You Xuan Trade Co., Ltd. Spiro-OMeTAD was purchased from Xi'an Polymer Light Technology Corp.\\n\\nReferring to the relevant literature, the FA0.85MA0.15Pb(I0.85Br0.15)3 mixed perovskite precursor solution was prepared by dissolving 1.4 M mixture of metal lead salts composed of 0.85 PbI2 and 0.15 PbBr2 and 1.3 M organic cations composed of 0.85 FAI and 0.15 MABr in anhydrous DMF:DMSO (4:1, volume ratio).\\n\\nThe etched FTO glass substrates were sequentially cleaned with detergent, deionized water, acetone, and 2-propanol in an ultrasonic bath for 10 min each. The glasses were then dried and treated by plasma for 5 min prior to use. An approximately 30 nm-thick TiO2 compact layer was sprayed on the hot FTO substrate using a 0.2 M titanium diisopropoxide-bis(acetylacetonate) solution and sintered at 450 \\u00b0C for 30 min. Afterward, according to our previous work, a mesoporous Na-treated TiO2 film was spin-coated at 5000 rpm for 50 s and then annealed at 500 \\u00b0C for 30 min. The perovskite layer was deposited via an anti-solvent method. Here, a 50 \\u03bcL perovskite precursor solution was spin-coated at 1000 rpm for 5 s and then at 4000 rpm for 60 s. During the second step, 120 \\u03bcL of chlorobenzene was dropped at the last 5th second. The substrates were then annealed at 120 \\u00b0C for 45 min. After cooling, the alternative hole transport layer (HTL) was deposited. According to a previous work, a Spiro-OMeTAD solution was prepared by dissolving 72.3 mg Spiro-OMeTAD powder in 1 ml chlorobenzene, to which 28.8 \\u03bcL 4-tert-butylpyridine and 17.5 \\u03bcL LiN(CF3SO2)2 (LITSFI) solutions (520 mg LiTSFI in 1 ml acetonitrile) were added. Thus, the 4-tert-butylpyridine and LiN(CF3SO2)2 (LITSFI) additives were added to the Spiro-OMeTAD solution. Then, the Spiro-OMeTAD solution was prepared according to a previous report and was deposited on the perovskite film at 3000 rpm for 30 s. The inorganic MnS HTL was prepared on top of the perovskite layer via thermal evaporation of MnS powder (Alfa Aesar, 99.9%) in vacuum of \\u223c1 \\u00d7 10\\u22124 torr using a thermal evaporator (Beijing Technol Science Co., Ltd). The evaporation rate was 0.9 \\u00c5 s\\u22121 and the Z-factor of MnS was 0.94. Finally, 80 nm gold was evaporated as the back electrode to form the entire device.\\n\\nThe crystal structures of MnS and perovskite films were characterized by an X-ray diffractometer (XRD-7000s, Shimadzu). The absorption and transmittance spectra of the films were measured by a UV-Vis spectrophotometer (Lambda 950, PerkinElmer). X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS) were performed using the XPS/UPS system (AXIS-ULTRA DLD-600 W, Shimadzu). The surface morphology and RMS roughness of perovskite and MnS thin films were characterized by atomic force microscopy (AFM, SPM9700, Shimadzu). The chemical composition and distribution of the constituents were observed by an electron probe microanalyzer (EPMA, EPMA-8050G, Shimadzu). The surface morphologies and microstructures of the perovskite and MnS films and the cross-sectional structure of perovskite solar cells were investigated by a field emission scanning electron microscope (FESEM, GeminiSEM300, Carl Zeiss) equipped with an energy-dispersive X-ray spectrometer (EDS). Fast component analysis of the MnS film was measured using an electron probe microanalyzer (EPMA-8050G, Shimadzu). The Ecopia HMS 5500 Hall system was applied to measure the room-temperature mobility and conductivity using the van der Pauw method with a magnetic field strength of 0.550 T. The photo-current density\\u2013voltage (J\\u2013V) characteristics were measured using a Keithley 2400 source meter under one-sun AM 1.5G (100 mW cm\\u22122) illumination with a solar light simulator (Model 71675-71580, Oriel Company). Photoluminescence (PL, excitation at 325 nm) and time-resolved photoluminescence (TRPL, excitation at 325 nm and emission at 760 m) spectra were obtained using a laser spectrometer (FLS 980, Edinburgh Instruments Ltd). The incident photon-to-electron conversion efficiency (IPCE) spectrum was measured using a Newport-74125 system (Newport Instrument). Electrochemical impedance spectroscopy (EIS, IviumStat 10800, Ivium Technologies) was performed under dark conditions and the frequency range was from 1 MHz to 100 MHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: FA0.85MA0.15PbBr0.45I2.55,\\n Perovskite_composition_short_form: FAMAPbBrI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 120,\\n Perovskite_deposition_thermal_annealing_time: 45,\\n HTL_stack_sequence: MnS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Evaporation,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The perovskite photovoltaic devices had a structure of ITO/HTL/MAPbI3/[6,6]-phenyl-C61-butyric acid methyl ester (PC60BM)/C60/2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP)/Al. Indium tin oxide (ITO) coated glass substrates were cleaned successively with deionized water, acetone, and UVO cleaner (Jelight 42). HTL was either PEDOT:PSS or c-OTPD plus TPACA. PEDOT:PSS was spincoated onto ITO substrates at 3000 rpm for 50 s and dried in air at 135 \\u00b0C for 20 min. We deposited a 15 nm thick c-OTPD layer with 0.25 wt% TPACA 1,2-dichlorobenzene (DCB) solution onto an ITO substrate using spin-coating. Then, the c-OTPD film was cross-linked using a UV lamp and dried in N2 at 100 \\u00b0C for 10 min.\\nPerovskite and fullerene layers were deposited on top of the PEDOT:PSS or c-OTPD:TPACA layer inside a N2 atmosphere. In the doctor blade coating process, the precursor solution was dropped onto the HTL-covered ITO substrate, and swiped linearly by a glass blade at a high speed of 0.75 cm s\\u22121 (27 m h\\u22121). The substrates were held at elevated temperature during blade deposition (typically 125 \\u00b0C). The thickness of the perovskite films during blade coating was controlled by perovskite precursor solution concentration and the depth of the blading channel. Methylammonium iodide (CH3NH3I, MAI) and PbI2 dissolved in dimethylformamide (DMF) were used as the perovskite precursor solution. We primarily use 1:1 molar ratio between PbI2 and methylammonium halide, at a mass ratio of 40% PbI2 (400 mg per 1 mL DMF) and 13.8% methylammonium halide. We used 10\\u201320 \\u03bcL of precursor solution per 2.25 mm2 substrate. This was much lower than 50\\u2013100 \\u03bcL typically used for spin coating of similar perovskite solutions over the same area substrate, which demonstrated the advantages of high material usage by doctor-blade coating.\\nThe as-deposited perovskite films were subsequently thermally annealed at 100 \\u00b0C for 60 minutes while undergoing solvent annealing with 10 \\u03bcL of DMF according to our previously reported method. PC60BM, dissolved in 2% by weight DCB solution, was spin-coated on top of the perovskite layer at 6000 rpm for 35 s. The resulting film was further thermally annealed at 100 \\u00b0C for 60 minutes without solvent annealing. C60 (20 nm thick) and BCP (8 nm) were deposited by thermal evaporation. Finally, 100 nm Al was deposited with a mask to provide a cell area of 7.25 mm2 for majority of our devices.\\nWe used simulated AM 1.5G irradiation provided by a xenon lamp (Oriel 67005) to measure the photocurrent of our devices. The light intensity was calibrated using a Si diode (Hamamatsu S1133). The current\\u2013voltage (IV) relationship was measured using a source-meter (Keithley 2400), with our standard test procedure of scanning at 0.2 V s\\u22121. The external quantum efficiency (EQE) was obtained using a Newport QE measurement kit. Impedance spectroscopy measurements were made using a LCR meter (Agilent E4980A) under the simulated 1 sun irradiation. A Rigaku D/Max-B Diffractometer with Co K\\u03b1 was used to perform X-ray diffraction (XRD). Topographical and cross-section SEM (Quanta 200 FEG ESEM) imaging was performed after sputtering of Au onto samples (Cressington 108). The film thickness was measured by stylus profilometry (Bruker Dektak XTL).\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Doctor blading,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 60,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.0725,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All materials were used as purchased without further purification unless specified otherwise. Organic solvents were purchased from Sigma Aldrich. Spiro-MeOTAD, CH3NH3I, and PbI2 were purchased from TCI.\\nPTZ-TPA was synthesized using a one-step Suzuki\\u2013Miyaura cross-coupling reaction. A mixture of 4-methoxy-N-(4-methoxyphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)aniline (0.560 g, 2.20 mmol), 3,7-dibromo-10-(4-octylphenyl)-10H-phenothiazine (0.545 g, 1.00 mmol), and Pd(PPh3)4 (0.028 g, 0.025 mmol) in toluene (10 mL) and a 2 M K2CO3 aqueous solution (5 mL) was stirred at 100 \\u00b0C for 24 h. After cooling down the reaction mixture to room temperature, the mixture was diluted with dichloromethane and washed with water. The organic layer was dried over Na2SO4 and the remaining solvent was evaporated. The crude product was purified by column chromatography (SiO2, petroleum ether/CH2Cl2 = 1/4 vol/vol) to obtain PTZ-TPA (0.789 g, 79.3% yield) as a yellow solid (1H NMR (500 MHz, CD2Cl2) \\u03b4 7.95\\u20136.10 (34H, m), 3.78 (12H, s), 2.73 (2H, s), 1.71 (2H, s), 1.30 (11H, s), 0.89 (3H, s); MS: m/z (M+) 992.544).\\nThe ultraviolet-visible (UV-vis) spectra of the solutions and of the solid thin films were obtained on a PerkinElmer Lambda750S spectrophotometer. Thermogravimetric analysis (TGA) was performed using a Discovery thermogravimetric analyzer. 1H NMR spectroscopy was performed using a Bruker DPX 400 MHz spectrometer. Matrix assisted laser desorption/ionization time-of-flight mass spectra were obtained on a Bruker Daltonics flexAnalysis. The highest occupied molecular orbital (HOMO) energy level of PTZ-TPA was measured using photoelectron yield spectroscopy under N2 (Model IPS-4). Steady-state photoluminescence spectra were measured using a FLS980 Spectrometer (Edinburgh Instruments). The samples were excited through the perovskite or PTZ-TPA layer with an excitation wavelength of 475 nm. Room-temperature photoluminescence (PL) decay curves were acquired for the perovskite films on fluorine doped tin oxide (FTO), for the perovskite films on PCBM/SnO2/FTO, of the Spiro-MeOTAD device, and of the PTZ-TPA/perovskite/PCBM/SnO2/FTO stack (excitation using a 405 nm-wavelength pulsed laser). The hole mobilities of PTZ-TPA and Spiro-MeOTAD were estimated using the space-charge limited current method with devices with a structure consisting of ITO/PEDOT:PSS/PTZ-TPA or Spiro-MeOTAD/Au. The current J\\u2013V curves of the devices were recorded using a Keithley 2400 source. Hole mobilities were calculated using the Mott\\u2013Gurney law by fitting eqn (1), where J is the current density, \\u03b50 is the permittivity of free space (8.85 \\u00d7 10\\u221212 F m\\u22121), \\u03b5 is the relative permittivity of the material (approaching 3 for organic semiconductors), \\u03bc is the hole mobility, V is the applied voltage, and d is the thickness of the active layer, respectively.\\n\\nPSCs were fabricated with the following structure: FTO/SnO2/PCBM/perovskite/PTZ-TPA/Au on patterned FTO glass. The FTO glass (with a sheet resistance of 20 \\u03a9 \\u25a1\\u22121, PV Tech, China) substrates were pre-cleaned using an ultrasonic bath of chlorobenzene and acetone followed by a treatment in an ultraviolet-ozone chamber (Novascan Company, USA) for 15 min. The SnO2 electron transport layer was applied following a previously reported procedure. SnCl2\\u00b72H2O in ethanol was used as a precursor solution (0.1 M). The precursor solution was spin-coated onto the substrate at a speed of 3000 rpm for 30 s and then the films were annealed under an ambient atmosphere at 180 \\u00b0C for 1 h. A thin layer of PCBM (10 nm) was prepared on the FTO/SnO2 surface at a speed of 2000 rpm and annealed at 100 \\u00b0C for 10 min. The PCBM solutions were prepared by dissolving 15 mg PCBM in 1 mL chlorobenzene. The perovskite (CH3NH3PbI3) layer (\\u223c320 nm) was then fabricated on the SnO2 film. The film was annealed at 90 \\u00b0C for 15 min. The hole-transporting materials PTZ-TPA (41 nm) were deposited by spin coating at 4000 rpm for 30 s from a chlorobenzene solution. The thickness of the photosensitive layer was measured using an Ambios Technology (USA) XP-2 profilometer. Finally, a 100 nm-thick Au film was deposited by thermal evaporation (Mbraun MB200) as the cathode. The active area (0.11 cm2) of the devices was determined by the overlap of FTO and the gold electrode. The current density\\u2013voltage (J\\u2013V) characteristics of the devices were measured with a computer-controlled Keithley (Zolix ss150 Solar Simulator) 236 source meter. The light source was a xenon lamp coupled with an AM1.5 solar spectrum filter; the optical power at the sample was 100 mW cm\\u22122. The incident photon-to-current conversion efficiency (IPCE) spectra were recorded using a solar cell quantum efficiency/external quantum efficiency measurement system (Zolix Solar cell scan 100) model SR830 DSP lock-in amplifier coupled with a WDG3 monochromator and a 500 W xenon lamp.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: SnO2-c | PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Unknown,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 90,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: PTZ-TPA,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.11,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"An aqueous dispersion of PEDOT:PSS (1.6 wt%, from H.C. Stark Baytron P, AI 4083) was obtained from Heraeus Co. Fullerene C60 was purchased from Solenne B. V., Netherlands. PbI2, PbBr2 (99.99%), CH(NH2)2CH3COO, HI(aq.), HBr(aq.) and BCP (2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline) were purchased from Aldrich Co. All materials were used as received except when specified. ITO-covered glass substrates were purchased from Ruilong Optoelectronic Co., Taiwan with photolithographic patterns designed by us. CH3NH3I, CH3NH3Br and CH(NH2)2I were synthesized from CH3NH2(aq.), CH(NH2)2CH3COO, HI(aq.) and HBr(aq.) with methods similar to those reported in the literature. GIXRD data were collected in the 2\\u03b8 range 5\\u00b0\\u201370\\u00b0 on a Bruker powder diffractometer (D8 Discover) using Cu K\\u03b11 radiation equipped with a 2D detector. The band gaps and Urbach energies of the perovskite films were obtained from their UV/Vis absorption spectra, which were recorded with a Hitachi U-4100 spectrometer. Scanning electron microscopy (SEM) images were taken with a Hitachi S-800 microscope at 10 kV. Samples for the SEM study were mounted on a metal stub with a piece of conducting tape and then coated with a thin layer of platinum film to avoid charging. The thickness of the films was measured from the cross-section SEM images. Nanosecond time-resolved photoluminescence (TR-PL) spectra were conducted using the time correlated single-photon counting (TCSPC) technique (UniRAM, Protrustech) along with the instrument response function of a 150 ps pulse duration and repetition rate of 20 MHz. The excitation wavelength was 405 nm. To prevent laser-induced thermal effects, the diameter of the spot size on the sample was increased to 50 \\u03bcm, and the excitation power was reduced to 0.1 mW. The spectra were taken with the perovskite film deposited on glass to eliminate the effects from the PEDOT:PSS hole transporter.\\n\\nThe MAPbI3 precursor solution (1.0 M) was prepared by adding equal moles of MAI and PbI2 to the anhydrous \\u03b3-butyrolactone (GBL)/dimethylsulfoxide mixture (DMSO) mixed solvent (volume ratio: 1:1). The MA1\\u2212xFAxPbI3 precursor solutions were made by replacing various amounts (0.1 mole, 0.2 mole, 0.3 mole and 0.4 mole, respectively) of MAI with FAI in the 1.0 M precursor solution. MA1\\u2212xFAxPbI3\\u2212yBry precursor solutions (without PbBr2) were formed when various amounts (0.15 mole, 0.3 mole and 0.45 mole, respectively) of MAI were replaced with MABr. The concentration (1.0 M) of all precursor solutions was the same. The precursor solutions composed of PbI2, PbBr2, MAI and FAI (as used by Jenet al.) in the GBL/DMSO (v/v: 1/1) mixed solvent with the exact same atomic stoichiometries as those using MAI, FAI, MABr and PbI2 as the starting materials were also prepared to study the effect of the starting materials on the photovoltaic performance of the resulting spin-coated films.\\n\\nPEDOT:PSS was spin-coated on top of cleaned, preheated ITO/glass at 5000 rpm for 30 s to form a hole-transporting layer (HTL) from its aqueous solution (1.6 wt%, AI 4083). After thermal annealing at 140 \\u00b0C for 10 min in air, in a glove box, the perovskite layer was deposited on top of the PEDOT:PSS film using one-step spin-coating combined with the anti-solvent washing method (1000 rpm for 10 s, 5000 rpm for 15 s, and in the last 5 s, toluene (100 \\u03bcl) was dropped on the film) to form a densely packed, fully-covered perovskite film. The perovskite film was thermal annealed (two-step) at 60 \\u00b0C for 30 s, 100 \\u00b0C for 30 s, and then 50 nm C60, 5 nm BCP and 100 nm Ag films were sequentially deposited on the perovskite to be the electron transporting layer (ETL), buffer layer and cathode electrode, respectively, using a high-vacuum thermal evaporator. The cells have an architecture of Glass/ITO/PEDOT:PSS/MA1\\u2212xFAxPbI3\\u2212yBry/C60/BCP/Ag with an active area of 0.2 cm \\u00d7 0.5 cm. The current density\\u2013voltage (J\\u2013V) curves were recorded using a Keithley 2400 source-measurement unit under a simulated AM 1.5G sun light at an intensity of 100 mW cm\\u22122 with a mask on the cell. The intensity of the simulated sunlight was calibrated using an NREL-certified Si solar cell (Oriel, 91150 V) with a KG-5 band pass color filter. The external quantum efficiency (EQE) or incident photo-to-current conversion efficiency (IPCE) was measured in air after sealing the device with a silica sealant and measuring immediately. A chopper and lock-in amplifier were used for the phase sensitive detection with the QE-R3011 measurement system (Enlitech Inc., Taiwan). The determination of the photovoltaic parameters and calibration of all the measuring facilities were the same as that reported previously.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60; 100,\\n Perovskite_deposition_thermal_annealing_time: 0.5; 0.5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Cesium carbonate, lead iodide, diphenylphosphinic acid (DPPA), oleylamine (OLA), oleic acid (OA), benzyl ether (BE), octadecene (ODE), toluene, ethanol, nickel oxide nanopowder, dimethylformamide (DMF), hydrochloric acid, zinc powder from Sigma Aldrich and TiO2 paste from Solaronix were of analytical grade and used as purchased.\\n\\nThe typical synthesis was done by placing 0.2 mmol PbI2 in 5 mL ODE, 0.5 mL OA and 0.5 mL OLA stirred in a 25 mL 3-necked flask. The flask content was degassed at 80 \\u00b0C for 30 min. Under a nitrogen flow, the temperature was raised to 150 \\u00b0C where 0.5 mL of Cs-OA (0.42 g Cs2CO3 dissolved in 8 mL at 150 \\u00b0C) was swiftly injected. After 10 s, the flask was quickly cooled down to room temperature in a cold water bath. The nanocrystals (NCs) were directly washed via centrifugation at 4500 rpm for 10 minutes followed by redispersion in toluene.\\n\\n2.3.1. OLA\\u2013OA addition by hot injection. Modification of OLA\\u2013OA addition was done using the same template as per the conventional approach. OLA and OA were added after drying PbI2 in ODE at 120 \\u00b0C for 1 hour. After all the PbI3 had dissolved under a nitrogen flow, the temperature was raised to 150 \\u00b0C. Cs-oleate (0.5 mL) as prepared above was quickly injected and the remaining steps followed those for conventional synthesis.\\n2.3.2. ODE and OA replacements. The solvents and ligands were changed from those used in conventional synthesis. ODE and OLA were replaced by toluene and benzene ether (BE) when the effect of other ligands such as DPPA was studied. Since DPPA is solid, the use of specific solvents capable of dissolving DPPA and the precursors is required. Nevertheless, the same protocol as that for the conventional approach was followed.\\n\\nFourier transform infrared (FTIR) spectroscopy was done using a Nicolet 1550 FT-IR spectrometer with a diamond crystal. UV-vis spectroscopy was done using a Cary 50, and the photoluminescence was studied on a Cary Eclipse with an excitation wavelength of 400 nm. The morphology of the synthesized nanoparticles was assessed using an FEI Tecnai T12 transmission electron microscope. The crystalline phase of the samples was determined using a PANalytical Empyrean X-ray diffractometer equipped with a Cu LFF HRDK40 X-ray tube.\\n\\nFTO-coated glass substrates were etched by sprinkling zinc powder on the surface followed by a few drops of HCl (2 M) to obtain the required electrode pattern. The substrates were sequentially sonicated in liquid detergent, distilled water, 2-propanol, acetone and ethanol for 10 min, respectively. Solaronix TiO2 paste was deposited onto the FTO coated substrate followed by sintering at 450 for 30 min. A CsPbI3 solution (5 mg mL\\u22121) was spin-coated on TiO2 at 1000 rpm for 30 s and then quickly baked at 100 \\u00b0C for about 1 min. This cycle was repeated until the active layer completely covered TiO2. The hole transporting layer was made by 3 cycles of spin-coating with NiO solution in dimethylformamide (0.5 M) onto the active layer at 1000 rpm for 15 s. Gold film was then deposited using a shadow mask via a sputter coater to a thickness of 50 nm. A device made of substrate-FTO-TiO2-CsPbI3/NiO-Au with a pattern area of 0.06 cm2 was fabricated. Contacts between FTO and gold were connected to the current\\u2013voltage measurement kit and the current characteristics were collected using a solar simulator set at 100 mW cm\\u22122 and under standard AM 1.5 conditions.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: CsPbI3,\\n Perovskite_composition_short_form: CsPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: Toluene,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 1,\\n HTL_stack_sequence: NiO,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.06,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methylammonium iodide (MAI) was provided by the Functional Phosphor Bank at Pukyong National University. If not stated otherwise, all chemicals were purchased from Aldrich. A 1.2 M perovskite precursor solution was prepared by dissolving equimolar PbI2 and MAI in a mixture of dimethyl sulfoxide (DMSO, 99.9%) and N,N-dimethylformamide (DMF, 99.8%) with the volume ratio as 1:9. The solution was stirred at 70 \\u00b0C overnight and filtered using 0.45 \\u03bcm nylon filters before use.\\n\\nThe solar cells were fabricated using the configuration of glass/indium tin oxide (ITO)/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/MAPbI3/phenyl-C61-butyric acid methyl ester (PC61BM)/Al. The glass/ITO substrates were cleaned with water, ethanol and acetone in an ultrasonic bath for 15 min in sequence, and subsequently treated in a UV-ozone cleaner for 15 min. A PEDOT:PSS (Baytron PVP Al 4083) layer of 50 nm thickness was fabricated by firstly spin coating PEDOT:PSS onto the substrates at 4500 rpm for 40 s and then annealing it at 150 \\u00b0C for 20 min. Then, the substrates were transferred into a N2-filled glovebox. The perovskite precursor solution was spin-coated onto the ITO/PEDOT:PSS layer at 5000 rpm for 10 s. Antisolvent treatment was performed according to our reported study. Then, the two as-cast precursor films were placed together face to face, and then annealed at 100 \\u00b0C for 10 min, meanwhile preheat balance weight for applied pressure was put on the top substrate. To apply different pressures, we simply used different balances with different weights on the top substrate. After growth completes, the substrates with perovskite films were physically separated for further use. For comparison, the as-cast precursor film was directly placed on a hot plate at 100 \\u00b0C for 10 min, which afforded the reference film. Finally, PC61BM (20 mg mL\\u22121 in chlorobenzene) was deposited by spin coating at 1500 rpm for 30 s, forming an 80 nm transporting layer. Al electrodes with a thickness of 100 nm were finally evaporated under high vacuum (<2 \\u00d7 10\\u22126 Torr) through a shadow mask. The device area is defined as 0.04 cm2.\\n\\nX-ray diffraction (XRD) experiments were performed by using a Philips X-ray diffractometer with Cu K\\u03b1 radiation. The surface morphologies of the perovskite films were obtained by SEM (S-2700, Hitachi, Japan). The UV-Vis absorption spectra of the perovskite films were collected on a Varian 5E UV/vis/NIR spectrophotometer. Photocurrent density\\u2013voltage (J\\u2013V) curves were obtained under AM 1.5 G irradiation (100 mW cm\\u22122) with a solar simulator and a Keithley 2400 source meter. The light intensity was adjusted using a calibrated Si solar cell. External quantum efficiency (EQE) was measured in direct current (dc) mode, where a xenon lamp was used as a light source for generating a monochromatic beam.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"PEDOT:PSS was obtained from Heraeus (Clevios P VP. Al 4083). The lead iodide (PbI2, beads, 99.999% trace metals basis) was purchased from Sigma Aldrich and methylammonium iodide (MAI, MS101000-10) was purchased from Dyesol Pty Ltd. All commercial products were used as received.\\n\\nThe small area (0.2 cm2) devices were fabricated on glass substrates (2.5 cm \\u00d7 2.5 cm) with a pre-patterned ITO layer (Xinyan, \\u223c18 \\u03a9 sq\\u22121). The electrodes were cleaned using Alconox (detergent) solution and a soft cloth before being sonicated in sequence with Alconox, de-ionized water, acetone and 2-propanol for 10 min each, and then dried under a nitrogen flow. For the large area devices 6 cm \\u00d7 6 cm glass substrates with an ITO layer (Kintec, \\u223c13 \\u03a9 sq\\u22121) were patterned by photolithography and etched with 5 M hydrochloric acid. The electrodes were cleaned using Alconox solution and a soft cloth before being sonicated in sequence with Alconox, de-ionized water, acetone and 2-propanol for 10 min each, and then dried under a nitrogen flow. For the large area devices with metal grids, 750 nm thick silver, gold or aluminum lines (width 550 \\u00b1 50 \\u03bcm, with the pitch between the lines being dependent on the number of lines) were thermally evaporated through a shadow mask at a vacuum of 10\\u22126 mbar. The substrates with the aluminum grid were then exposed to a UV-ozone plasma (MBraun, MB UV-O3) for 15 min to grow the oxide layer. Each of the substrates were coated with a 30 \\u00b1 5 nm PEDOT:PSS layer by spin-coating at 5000 rpm for 30 s before being dried on a hot plate at 170 \\u00b0C for 10 min. All the substrates were then transferred into a nitrogen filled glove box for device fabrication (O2 < 5 ppm, H2O < 5 ppm). CH3NH3PbI3 thin films were spin-coated as per the method reported by Jeon et al. 1.2 M PbI2 and MAI (e.g., 553 mg PbI2 and 191 mg MAI in 1 mL of solvent) were dissolved in a mixed solvent of \\u03b3-butyrolactone (GBL) and dimethyl sulfoxide (DMSO) (7:3 v/v) with stirring and heating at 60 \\u00b0C for 2 h. The solution was then dispensed onto the substrate until it was fully covered and spin-coated at 3000 rpm. After 42 s 1.7 mL of toluene was dispensed onto the middle of the spinning organohalide perovskite film. After a further 38 s of spinning at 3000 rpm the spin speed was increased to 5000 rpm for 20 s to dry the film. The substrates were then further dried on a hot plate at 100 \\u00b0C to fully convert the film to the organohalide perovskite. In the next step a 10 mg mL\\u22121 PC60BM in toluene solution was spin-coated onto the CH3NH3PbI3 layer at a spin speed of 1000 rpm for 20 s. The devices were heated on a hot plate at 70 \\u00b0C for 10 min. Finally, 1 nm of LiF and 200 nm of Ag were deposited by thermal evaporation under a 10\\u22126 mbar vacuum with a shadow mask to complete the device.\\n\\nThe morphology of the organohalide perovskite films and the cross-sectional structure of the solar cells were measured using a Hitachi SU3500 scanning electron microscopy (SEM) and a Jeol JSM-7100F field-emission scanning electron microscopy (FESEM) (Jeol JSM-7100F). The X-ray photoelectron spectroscopy (XPS) data were collected on a Kratos AXIS Ultra with a monochromatic Al X-ray source at 150 W and analyzed with CasaXPS software. The water contact angle of the grid lines were measured by a PSS OCA20 optical contact-measuring system. For the thickness mapping a SCI FilmTek 2000M spectroscopic reflectometer was used.\\n\\nCurrent density\\u2013voltage (JV) characteristics were acquired in a nitrogen filled glovebox (O2 < 1 ppm, H2O < 1 ppm) using a Keithley 2400 Source Measure Unit and Agilent B1500A semiconductor analyzer. The simulated Air Mass 1.5 Global (AM 1.5 G) illumination was provided by an Abet Sun 2000 Solar Simulator. The light intensity used throughout was \\u223c1000 W m\\u22122 (the exact number being used for efficiency calculations) as determined by an NREL-calibrated silicon reference cell with a KG5 filter. For the large area devices (25 cm2) the JV curves were measured using an Agilent B1500A semiconductor analyzer with a 4-wire configuration to eliminate the effect of the cable resistances and SMU internal impedance in the measurement circuit. The reason for this is that for the large area devices the current flowing in the circuit was much higher than for the small area devices resulting in a larger voltage drop over the cable resistance and SMU impedance, and thus the four-wire configuration compensates for the voltage drop. For the 0.2 cm2 devices 10 samples and for the 25 cm2 devices three samples were fabricated and tested. EQEs were measured with a QEX7 setup from PV Measurements Inc., using a calibrated photodiode. The area of the focused beam was approximately 0.15 cm2. The white light short circuit current and integrated small perturbation EQE currents were determined to be within 10% of each other as a final validation of the measurement protocols.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | LiF,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 25,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"The ZnO nanoparticles were prepared according to the work of Janssen et al. Lithium salts (>99.0%) were purchased from Aldrich. Lead iodide (beads, \\u221210 mesh, 99.999% trace metals basis), HC(NH2)2I (>98.0%) and spiro-OMeTAD (2,2\\u2032,7,7\\u2032-tetrakis-(N,N-di-4-methoxyphenylamino)-9,9\\u2032-spirobifuorene, >99.0%) were purchased from Xi'an Polymer Light Technology Corp. (PLT). We will hereafter denote this spiro-OMeTAD as Spiro. P3HT was purchased from Rieke Metals. Ultradry solvents: N,N-dimethyl formamide (DMF, >99.9%) and isopropanol (>99.9%) were obtained from J&K and Acros, respectively. All the chemicals and solvents were kept in a glove-box before starting our experiment.\\n\\nPre-patterned indium tin oxide (ITO)-covered glass substrates were cleaned for about 20 min in detergent followed by ultrasonic cleaning in deionized water, acetone, and 2-propanol in sequence for 20 min each. Then the ITO substrates were treated with plasma for about 5 min. The ZnO solution was spin-coated on ITO substrates at 1500 rpm for 50 s, followed by baking at 150 \\u00b0C for 15 min. A 460 mg mL\\u22121 solution of PbI2 in DMF with TBP (120 \\u03bcL TBP in 1 mL DMF) was then spin-coated on the top of the ZnO layer at 4000 rpm for 30 s in the glove-box. The PbI2-coated ZnO thin film was then annealed at 70 \\u00b0C for 10 min. The film was preheated at 100 \\u00b0C for 3 min before dipping into a FAI 2-propanol solution (15 mg mL\\u22121) for 20 s followed by annealing at 145 \\u00b0C for 15 min to obtain the desired crystallite formation.\\nAs a hole-transporting material (HTM), a Spiro solution (80 mg of Spiro, 10.5 \\u03bcL of 4-tert-butylpyridine (tBP), and 46.5 \\u03bcL of a lithium bis(tri-fluoromethanesulfonyl)imide (Li-TFSI) solution (170 mg Li-TFSI/1 mL acetonitrile) in 1 mL chlorobenzene) was spin-coated at 4000 rpm for 30 s and a P3HT solution (15 mg mL\\u22121 in chlorobenzene) was spin-coated at 3000 rpm for 30 on the HC(NH2)2PbI3. The substrates with HTMs were left overnight in dry air in the dark at room temperature. Finally, 80 nm thick Ag was thermally evaporated through a shadow mask defining an active area of 0.04 cm2 on the top of the HTL to produce a complete PeSC device.\\n\\nThe current\\u2013voltage characteristics of the solar cells were measured by using a computer-controlled Keithley 2400 source meter measurement system with an AM 1.5G filter at a calibrated intensity of 100 mW cm\\u22122 illumination, as determined using a standard silicon reference cell (91150V Oriel Instruments). EQE spectra were measured in air under short-circuit conditions using a commercial EQE setup (Crowntech QTest Station 1000AD), which was equipped with a 100 W Xe arc lamp, filter wheel, and monochromator. Monochromated light was chopped at a frequency of 80 Hz and photocurrents measured using a lock-in amplifier. The setup was calibrated against a certified silicon reference diode.\\nFor the transient photocurrent measurements, the devices were illuminated from the ITO side by a 10 ns pulse width laser flash (Continuum Minilite TM Nd:YAG, 10 Hz repetition rate) at 532 nm. The light intensity on the sample varies under a series of optical density filters. The devices were connected to the 50 \\u03a9 input terminal of an oscilloscope.\\nThe CELIV set up consists of a pulsed laser (Continuum Minilite TM Nd:YAG), a synthesized function generator (Stanford Research System DS345), a digital delay generator (Stanford Research System DG645), and an oscilloscope (Tektronix MSO 4054) for signal observation and recording. Photo-CELIV measurements are carried out under ambient conditions, and samples are irradiated through the ITO side by a 10 ns, 532 nm laser flash. The linearly increasing voltage with an offset voltage (Uoffset) of 0.4 V and a maximum voltage (Umax) of 3.6 V (P3HT PeSC), and Uoffset = 0.6 V and Umax = 3.4 V (Spiro PeSC) is applied to the device, while the Ag electrode is grounded. The chosen Uoffset exactly compensates for the built-in potential (Vbi) of the devices, thereby nulling the internal electric field before the charge carrier extraction.\\n\\nThe thicknesses of ITO, ZnO, FAPbI3, P3HT, Spiro and Ag layers were estimated using a Veeco Dektak 150 surface profilometer.\\nThe reflectance and transmittance spectra were measured with a Shimadzu UV-3600 spectrophotometer between 300 and 900 nm with a 1 nm increment.\\nEllipsometry measurements were carried out with a Horiba Jobin Yvon UVISEL 2 ellipsometer at incident angles of 70\\u00b0 for photon energies between 0.6 and 6 eV with a 30 meV increment. The ZnO, Spiro and P3HT films were prepared following the aforementioned processes except for using clean Si wafers as the substrate. It should be noted that the FAPbI3 films were prepared on the substrate of Si/ZnO, in order to keep the FAPbI3 films same as that in the devices. Modelling of the data was performed using Deltapsi2 software by HORIBA Scientific Company. Before the films were measured, the bare silicon oxide layer was measured, and a thickness of 2 nm was obtained. All measurements were done at room temperature (\\u223c298 K).\\nSteady-state fluorescence spectra were measured on a Shimadzu RF-5301PC spectrophotometer. Time-resolved photoluminescence (TrPL) spectra were obtained on a PL spectrometer (Edinburgh Instruments, FLS 980), excited with a picosecond pulsed diode laser (EPL-375). A Hamamatsu C5680-04 streak camera was used for TPL. The X-ray diffraction (XRD) patterns were recorded on a Rigaku SmartLab X-ray diffractometer with Cu K\\u03b1 radiation (\\u03bb = 1.5418 \\u00c5) at 25 \\u00b0C. The data were collected with a 0.01\\u00b0 step size (2\\u03b8). A field emission scanning electron microscope (Hitachi SU8020) was used to acquire SEM images.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: ZnO-np,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: FAPbI3,\\n Perovskite_composition_short_form: FAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; TBP >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 145.0,\\n Perovskite_deposition_thermal_annealing_time: 10.0 >> 15.0,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"2.1.1. Materials. An aqueous dispersion of PEDOT:PSS (AI 4083) was obtained from Heraeus Co. Fullerene derivatives (PC61BM (99.8%)) were purchased from Nano-C Co. TOPD, bis(2,4-pentanedionato)molybdenum(VI) dioxide (MoO2(acac)2) and PbI2 (99.999%) were purchased from Alfa Aesar. All these commercially available materials were used as received without further purification.\\n2.1.2. Synthesis of CH3NH3I. CH3NH3I was synthesized through the reaction of 28.7 mL methylamine (40 wt% in methanol, Aladdin) and 29.8 mL hydroiodic acid (57 wt% in water, Aladdin) under nitrogen atmosphere in 250 mL round-bottom flask in an ice bath for 2 h with stirring. The crystals of methylammonium iodide (CH3NH3I) were collected using a rotary evaporator at 50 \\u00b0C for 2 h to remove the solvent. The product was dissolved in ethanol, followed by re-crystallization by diethyl ether. The crystals were filtered and washed three times with diethyl ether. At last, the solid was dried at 60 \\u00b0C in vacuum oven overnight. The detailed process is shown in .\\n\\nITO glasses (AGC, 11-8, 7 \\u03a9 sq\\u22121) were patterned by laser cutting and ultrasonically cleaned with detergent, deionized water, acetone and isopropanol for 20 min, sequentially, followed by plasma cleaning for 20 min prior to use. 5 mg mL\\u22121 of MoO2(acac)2 isopropanol solution was spin-coated at 4000 rpm for 30 s on the precleaned ITO glass, and then baked in air at 150 \\u00b0C for 10 min to prepared s-MoOx film, followed by plasma cleaning for 1 min. Subsequently, PEDOT:PSS aqueous solution filtered through a 0.22 \\u03bcm filter was spin-coated at 4000 rpm for 30 s on the s-MoOx film, and then baked at 120 \\u00b0C in air for 15 min. Then the ITO/s-MoOx/PEDOT:PSS substrate was transferred to a nitrogen-filled glove-box for the perovskite film deposition. 461 mg of PbI2, 159 mg of CH3NH3I was dissolved in a mixed solvent of DMF and DMSO (7:3, v/v) at 60 \\u00b0C with stirring for 12 h to prepare perovskite precursor. 40 \\u03bcL completely dissolved perovskite precursor solution was spin-coated on the PEDOT:PSS layer at 500 rpm for 3 s, followed by 4000 rpm for 30 s. 240 \\u03bcL of chlorobenzene was quickly dripped on the rotating substrate at the beginning of 8\\u201312 s in the second spin coating step. The substrate was immediately dried on a hot plate at 100 \\u00b0C for 10 min and obtained a dense CH3NH3PbI3 film. After that, 20 mg mL\\u22121 of PCBM solution in chlorobenzene was spin-coated at 1000 rpm for 20 s on the perovskite absorber layer. The TOPD buffer layer was prepared by spin-coating a 3 mg mL\\u22121 TOPD isopropanol solution on the PCBM at 4000 rpm for 30 s and then stays in glove box for 24 hours for solvent annealing. The thickness of the TOPD layer was about 10 nm. Finally, Ag electrode was deposited by using thermal evaporator at a constant evaporation rate of 1 \\u00c5 s\\u22121.\\n\\nScanning electron microscope (SEM) images were obtained by using FE-SEM (ZEISSUltra55). Transmittance spectra were recorded with an integrating sphere system (Ocean Optics, USA) in the 400\\u2013900 nm range. X-ray diffraction (XRD) analysis was performed on a PANalytical X'Pert PRO diffractometer with the Cu-K radiation at a scan rate of 4\\u00b0 min\\u22121. Steady-state PL spectra were measured using an excitation wavelength of 467 nm in an HORIBAfluorolog3. TRPL measured by Time Correlated Single Photon Counting (TCSPC, picoharp300) with a femto second laser source. J\\u2013V curves measurements were carried out using Keithley 2400 at room temperature under AM1.5G illuminations (1000 W m\\u22122) from a solar simulator (Newport, 91160), which was calibrated using a standard silicon solar cell device by the NREL. The incident photon to converted current efficiency (IPCE) spectra was measured from 300\\u2013850 nm using a Xe source (Newport, 66902). The light intensity at each wavelength was calibrated with a standard single-crystal Si photovoltaic cell. The IPCE measurement was performed under ambient atmosphere at room temperature. EIS was measured with a CHI6601 Electrochemical Workstation with an AC signal of 200 mV in the frequency range of 0.1 Hz to 1 MHz.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | TOPD,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: MoOx | PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating | Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"15.756 mL of aluminum tri-sec-butoxide (Aldrich, 97%) was dissolved in 200 mL of deionized (DI) water. A semi-transparent white precipitate was instantly formed, during stirring for 5 h. 8.56 ml of ammonium hydroxide solution was added dropwise and stirred for a further 6 h, which yielded a white precipitate. The solution was transferred to a high pressure vessel and autoclaved at 240 \\u00b0C for 16 h. The water in the resultant Al2O3 colloidal solution was replaced with ethanol, to which terpineol (TP, 99.5%, Aldrich), ethyl cellulose (EC, 46 cp, Aldrich) and lauric acid (LA, 96%, Fluka) were added with the weight ratio of Al2O3:TP:EC:LA = 1.25:6:0.9:0.1. A viscous paste was obtained by evaporation of ethanol, which was treated using a three-roll mill for 20 min. TiO2 nanoparticles (diameter of \\u223c50 nm) were synthesized by a two-step hydrothermal method as described elsewhere. The seed particles (diameter of \\u223c20 nm) were hydrothermally synthesized by acetic acid-catalyzed hydrolysis of titanium isopropoxide (97%, Aldrich) at 230 \\u00b0C for 12 h. The seed particles were washed with ethanol and collected by centrifugation. The same hydrothermal process was repeated with the solution including the seed particles to increase the size. TiO2 paste was prepared by mixing the TiO2 particles (\\u223c50 nm) with TP, EC and LA with the weight ratio of TiO2:TP:EC:LA = 1.25:6:0.9:0.1. The paste was further treated with a three-roll mill for 40 min.\\n\\nCH3NH3I was synthesized by reacting with methyl amine (40 wt% in methanol, TCI) and hydroiodic acid (57 wt% in water, Aldrich) in a 250 ml round-bottomed flask at 0 \\u00b0C for 2 h, according to a method described elsewhere. The precipitate was recovered by evaporation of the solvent at 90 \\u00b0C for 75 min, and was washed with diethyl ether three times for 30 min. CH3NH3I was recrystallized in ethanol and diethyl ether solution, and collected by drying at 60 \\u00b0C for 12 h in a vacuum oven.\\n\\nFTO glass (Pilkington, TEC-8, 8 \\u03a9 sq\\u22121) with dimensions of 4.8 \\u00d7 4.8 cm2 was treated in a UVO cleaner for 15 min, cleaned with a detergent solution, washed with acetone, and then finally cleaned in an ethanol bath under sonication for 25 min. To make the compact TiO2 blocking layer (bl-TiO2), 0.15 M titanium diisopropoxide bis(acetylacetonate) (75 wt% in 2-propanol, Aldrich) in 1-butanol (99.8%, Aldrich) solution was spin-coated on the FTO substrate at 700 rpm for 8 s, 1000 rpm for 10 s, and 2000 rpm for 40 s, then annealed at 125 \\u00b0C for 5 min. The mesoporous oxide films were formed by spin-coating the diluted paste (0.16 g paste ml\\u22121 ethanol) on the bl-TiO2 layer at a spinning rate of 2000 rpm for 20 s, followed by drying at 125 \\u00b0C for 5 min and then annealing at 550 \\u00b0C for 1 h in a muffle furnace. The thicknesses of the annealed oxide films were determined to be around 300 \\u00b1 50 nm as measured by cross-sectional scanning electron microscopy (SEM). Bare TiO2 and Al2O3 films were prepared along with the admixture films. For the admixture films, the diluted TiO2 paste was mixed with the diluted Al2O3 paste in the weight ratio of 3:1 (25% Al2O3, 0.75 g TiO2 and 0.25 g Al2O3), 1:1 (50% Al2O3) and 1:3 (75% Al2O3), and sonicated using a micro Ti tip for 1 min.\\nMAPbI3 was fabricated from the Lewis base adduct PbI2 according to a method described elsewhere. PbI2 (99.9985%, Alfa Aesar), CH3NH3I and dimethyl sulfoxide (DMSO, 99.5%, Aldrich) were mixed with a 1:1:1 molar ratio in N,N-dimethylformamide (DMF, 99.8%, Aldrich), and spin-coated on the mesoporous oxide films at 4000 rpm for 30 s. In order to form a MAI\\u00b7PbI2\\u00b7DMSO adduct film, diethyl ether was added dropwise after 10 s spinning. DMSO was eliminated by careful heat-treatment at 65 \\u00b0C for 1 min and 100 \\u00b0C for 9 min. A solution of 72.3 mg 2,2\\u20327,7\\u2032-tetrakis-(N,N-di-p-methoxyphenylamine)-9,9\\u2032-spiro-bifluorene (spiro-MeOTAD) was prepared in 1 ml chlorobenzene including 28.8 \\u03bcl 4-tert-butyl pyridine (TBP) and 17.5 \\u03bcl lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) solution (520 mg in 1 ml acetonitrile (99.8%, Aldrich)). The spiro-MeOTAD solution was spin-coated on the MAPbI3 film at 4000 rpm for 25 s. Finally, silver was thermally evaporated on the top of the spiro-MeOTAD at rate of 0.3 \\u00c5 s\\u22121 for about 1.5 h.\\n\\nPhotocurrent density and voltage were measured using a Keithley 2400 source meter under AM 1.5 G one-sun illumination (100 mW cm\\u22122) provided by a solar simulator (Newport 3A class AAA). A 450 W xenon lamp (Newport 6279NS) was used as a light source. The light intensity was adjusted using a NREL-calibrated Si solar cell equipped with a KG-2 filter. During the measurement the device was covered with a metal aperture mask (area = 0.125 cm2). External quantum efficiency (EQE) was measured using a EQE system (PV measurements), where a 75 W xenon lamp (USIO, Japan) was used as a light source for generating a monochromatic beam. Calibration was conducted using a silicon photodiode, which was calibrated using the NIST-calibrated photodiode G 425 as a standard. EQE data were collected at DC mode.\\nX-Ray diffraction (XRD) data were collected using a Bruker AXS (D8 advance, Bruker Corporation) with Cu K\\u03b1 radiation (\\u03bb = 1.5405 \\u00c5) at a scan rate of 4\\u00b0 min\\u22121. UV-vis absorbance was measured using a UV spectrophotometer (PerkinElmer, lamda35) in the wavelength range from 300 nm to 900 nm. Time-integrated and time-resolved photoluminescence (PL) was measured by a fluorescence lifetime spectrometer (Quantaurus-Tau C11367-12, HAMAMATSU). The films were photo-excited with a 464 nm laser (PLP-10, HAMAMATSU) pulsed at a frequency of 10 MHz. The PL was detected by high sensitivity photon counting near IR detector. Morphology and elemental analyses were performed using a high-resolution scanning electron microscope (FE-SEM; JSM-7600F, JEOL) combined with an energy dispersive X-ray spectrometer (EDS) and a focused ion beam assisted SEM (FIB-SEM, Zeiss Auriga). The pore volume and pore size of mesoporous films were measured by a Brunauer\\u2013Emmett\\u2013Teller (BET) analyzer (Micromeritics Instrument Corp. ASAP 2020).\\nImpedance spectroscopy (IS) measurements were carried out with a potentiostat/galvanostat (PGSTAT 128N, Autolab, Eco-Chemie) under one-sun illumination (100 mW cm\\u22122). To investigate the charge behavior near open-circuit voltage, a DC bias voltage ranging from 0.7 V to 0.8 V was applied with a potential step of 100 mV, where an AC 20 mV small perturbation signal overlapped with a frequency from 0.1 Hz to 1 MHz. An equilibration time of 10 s was applied after every step. The obtained Nyquist plots were fitted with an equivalent circuit comprising a series resistance (Rs) and three series connected R\\u2013C (resistance and capacitance in parallel) components using Z-View software. Recombination resistance was obtained from the last arc shown in the low frequency range.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 65; 100,\\n Perovskite_deposition_thermal_annealing_time: 1.0; 9.0,\\n HTL_stack_sequence: Spiro-MeOTAD,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.125,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Fluorine doped tin oxide (FTO) coated glasses (1.5 cm x 1.5 cm) were etched by using hydrochloric acid and zinc powder to obtain two separated the electrodes. The wet-etched FTO glasses were cleaned ultrasonically in detergent solution, acetone, isopropyl alcohol for 15 min sequentially and then rinsed with deionized water for 15 min. Clean substrates were dried with nitrogen gun and subsequently treated with oxygen plasma for 5 min to eliminate organic traces. Onto cleaned FTO glasses, thin c-TiO2 layer was spin coated by using solution of titanium (IV) isopropoxide (99.9%, Sigma-Aldrich, as received) and acetyl acetone (99.5%, Sigma-Aldrich) in absolute ethanol at 1500 rpm for 20 s, followed at 2000 rpm for 20 s. Before drying, the coated substrates were sintered 450\\u00b0 C for 30 min to form a compact n-type layer of TiO2 in air.\\nThe SAM modified substrate were fabricated by a simple method, which can be seen in Fig. 2 . Firstly, 1 mM of SAM solutions were prepared by solving 1-OMe, 2-OMe and 3-OMe in dimethyl sulfoxide (DMSO). c-TiO2 coated substrates were immersed in SAM solutions for overnight to perform covalently bonding. Then, substrates were removed from solutions and rinsed to eliminate physically absorbed molecules with DMSO, acetone and DMSO, respectively. The perovskite absorber layer and hole transport layer (HTL) was deposited under N2 atmosphere in glovebox onto SAM-modified and non-modified c-TiO2 coated FTO. MAPbI3 pre-mixed perovskite solution was prepared by mixing 1.54 mol of CH3NH3I (Dyesol) and 1.23 mol of PbI2 (99.999%, Alfa Aesar,) in 2.5 mL \\u0263-butyrolactone (GBL, anhydrous, 99.9%, Sigma Aldrich) and stirred at room temperature for overnight. 70 \\u03bcL perovskite solution was deposited by spin-coating at 4000 rpm for 50 s and 70 \\u03bcL toluene was dropped rapidly in one-shot at last 35 s of spinning substrate to obtain a uniform and flat intermediate-phase film. Then perovskite coated substrate were annealed at 85\\u00b0 C for 15 min. The dopant free hole transporter material P3HT solution was prepared by dissolving 20 mg of poly(3-hexylthiophene-2,5-diyl) in 1 mL of chlorobenzene and mixed at 70\\u00b0 C for overnight. Prepared solution was spin-coated at 1500 rpm for 15 s and at 2000 rpm for 15 s. Finally, 10 nm of MoO3 and 100 nm of Ag were thermally evaporated on top of the HTM layer, respectively.\\n\\nThe structural and morphological analyses of as-prepared films were carried out by contact angle goniometer (Kruss Easy Drop), X-ray diffraction (XRD, Bruker D8 Advance), scanning electron microscope (SEM, Zeiss Evo). The optical properties were characterized by ultraviolet-visible (UV\\u2013vis) absorption spectroscopy (Biochrom Libra S22 spectrometer). The X-ray Photoelectron Spectroscopy (XPS) results were recorded by SPECS EA 300 equipped with Al monochromatic anode. Atomic force microscope (AFM) analyses were performed by using NT-MDT AFM NTEGRA Solaris in \\u201ctapping\\u201d mode and work function measurements of SAM modified and non-modified substrates were carried out in Kelvin Probe mode. Bruker DektakXT surface profilometer was used to measure thin film thicknesses. The photovoltaic J\\u2013V characteristics of as-fabricated perovskite solar cells without any encapsulation were tested under N2 ambient in glovebox using Keithley 2400 source meter. AM1.5 light source (Atlas) was used as solar simulator. The external quantum efficiencies were recorded as a function of wavelength from 350 nm to 800 nm under N2 by using a monochromatic light from Xenon-lamp connected to EG&G 7260 DSP Lock-in amplifier to measure the photocurrent response.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | 1-OMe-SAM,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Dipp-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 85,\\n Perovskite_deposition_thermal_annealing_time: 15,\\n HTL_stack_sequence: P3HT,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: MoO3 | Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation | Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"CH3NH3I (Dyesoltimo), PbI2 (99.99%, TCI Co., Ltd.), \\u03b3- butyrolactone (GBL, Sigma Aldrich), and dimethyl sulfoxide (DMSO, Junsei) were used to generate the CH3NH3PbI3 (MAPbI3) solution. The hole transport layer of PEDOT:PSS (AI4083 was supplied by the ECS group) and the electron transport layer of 6,6-phenyl-C71 butyric acid methyl ester (PC71BM)/TiOx (precursor: Titanium(VI) isopropoxide, Sigma Aldrich) were used for an efficient structure. 1-hydroxycyclohexyl phenyl ketone (HCPK, Aldrich) and aliphatic urethane diacrylate oligomer (EB 9270, ENTIS), and perfluoropolyether (PFPE, Aldrich) were used for the synthesis of the modified (hydrophobic) polyurethane acrylate (PUA) mold films. The modified PUA film of relatively hydrophobic property was fabricated using a method reported previously [33].\\n\\nITO glass substrates were cleaned using dishwasher detergent, and ultrasonicated under deionized water, acetone, and isopropanol sequentially for 20\\u202fmin each. To compare between transfer printing and spin-coating, the PEDOT:PSS was diluted in methanol at a 1:1\\u202fvol ratio, and coated onto the UVO-treated PFPE-PUA and ITO, respectively, at 3500\\u202frpm for 60\\u202fs with a thickness of 30\\u202fnm. Subsequently, the PEDOT:PSS layer was transferred from PFPE-PUA to the ITO surface under 95\\u202f\\u00b0C and uniform pressure. The PEDOT:PSS-deposited substrates were annealed on a hot plate at 140\\u202f\\u00b0C for 10\\u202fmin, to form a thin film with a thickness of 30\\u202fnm. The MAPbI3 solution was composed of CH3NH3I and PbI2 (1.06:1 mol.%) in GBL and DMSO (7:3\\u202fvol ratio), with a molar concentration of 1.4\\u202fmol/L at room temperature for 12\\u202fh. To generate the perovskite film, a solution of MAPbI3 was spun on the PEDOT:PSS film at 1000\\u202frpm for 30\\u202fs, and subsequently 5000\\u202frpm for 30\\u202fs with the additional treatment of toluene. Following that, the substrates were placed on a hot plate at 100\\u202f\\u00b0C for 5\\u202fmin, to form the crystallized MAPbI3 film with a thickness of 300\\u202fnm. To fabricate PC71BM with a thickness of 30\\u202fnm, the PC71BM solution was dissolved in chlorobenzene with a concentration of 20\\u202fmg/mL, and spin-coated onto the surface of MAPbI3 at 2000\\u202frpm for 40\\u202fs. Subsequently, the TiOx layer with a thickness of \\u223c10\\u202fnm was formed at 5000\\u202frpm for 40\\u202fs, using a molar concentration of 25\\u202fmmol/L. Finally, an Al cathode was deposited thermally under 1.9\\u202f\\u00d7\\u202f10\\u22126\\u202fTorr with a thickness of 100\\u202fnm by thermal evaporation.\\n\\nThe surface morphology and roughness of several thin films were observed by atomic force microscope (AFM) in the noncontact mode (Park NX10), and field emission scanning electron microscopy (FE-SEM) (SIGMA model from Carl Zeiss, Inc.) at 5\\u202fkV. The contact angles of water droplets on the mold film and PEDOT:PSS thin film were measured using a contact angle analyzer (SEO, Phoenix 300 THOUCH). The electrical performances of the PSCs were measured under a solar simulator (Peccell Technologies, Inc., PEC-L01) with air mass 1.5 global (AM 1.5 G) at an intensity of 100\\u202fmW/cm2, which was calibrated by a silicon reference cell. The current-density\\u2013voltage characteristics of the PSCs were measured using an electrical measurement system (ZIVE SP1). The EQE was measured after power calibration (ABET Technologies, Inc., LS150) with a monochromator (Dongwoo Optron Co. Ltd., MonoRa-500i). The crystallinity of the perovskite thin film was analyzed by XRD spectra (Bruker-AXS, New D8-Advance). The X-ray photoelectron spectra (XPS) was recorded with a K-Alpha\\u202f+\\u202fspectrometer (ThermoFisher Scientific). The PL spectra were measured by Raman microscopy (Xperam200 (Nanobase Inc.)). The laser wavelength was 642\\u202fnm, and the power was 0.3 mW for each device. The magnification of the object lens was 40\\u00d7. We calculated the average of ten datasets of the Raman spectra in the same position for each sample.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | TiO2-c,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMSO; GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 5,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.15,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Device Fabrication: The ITO-coated glass substrates (sheet resistance: 6.4\\u202f\\u03a9 sq\\u20131) were cleaned ultrasonically with abstergent aqueous solution, deionized water, acetone, and isopropyl alcohol for 20\\u202fmin, and then dried under a stream of N2. The substrates were then cleaned with air plasma for 10\\u202fmin. A NiOx film (ca. 20\\u202fnm) was prepared by spin-coating a solution containing the NiOx precursor [nickel(II) acetylacetonate (129\\u202fmg) dissolved in EtOH (5\\u202fmL) containing HCl (38\\u202fwt%, 50\\u202f\\u03bcL)]. The NiOx-coated substrates were then baked at various temperature for various periods (min) in air [44]. The MAPbI3 precursor solutions (with or without 3\\u202fwt% urea) were prepared by dissolving 1.2\\u202fM PbI2 and MAI (molar ratio, 1:1) in anhydrous DMF/DMSO (4:1). The solution was stirred at 60\\u202f\\u00b0C for 2\\u202fh in an Ar-filled glove box. The perovskite precursor solutions were spin-coated on the NiOx-coated substrates in two steps (step 1: 2000\\u202frpm for 10\\u202fs; step 2: 4000\\u202frpm for 20\\u202fs), and then toluene (100\\u202f\\u03bcL) was applied rapidly to the substrates to induce fast crystallization. Finally, the samples were annealed at 100\\u202f\\u00b0C for 10\\u202fmin to complete the transformation to the perovskite [53]. PC61BM (20\\u202fmg\\u202fmL\\u22121 in anhydrous chlorobenzene) was deposited; following the deposition of BCP (2\\u202fmg\\u202fmL\\u22121 in IPA), spin-coating was performed at 6000\\u202frpm for 30\\u202fs. Finally, the device was completed through the evaporation of Ag or Au contact electrodes (100\\u202fnm) at a vacuum level of 10\\u20137 Pa through a shadow mask. The active area of this electrode was fixed at 10\\u202fmm2.\\n\\nThe cell performance was measured inside a glove box. The current\\u2013voltage (I\\u2013V) properties of the devices were measured using a computer-controlled Keithley 2400 source measurement unit (SMU) and an Enlitech simulator (AAA Class Solar Simulators) under AM 1.5 illumination (1000\\u202fW\\u202fm\\u22122). The illumination intensity was calibrated using a standard Si reference cell and a KG-5 filter. EQEs were measured using an Enlitech QE-R spectral response measurement system to calibrate the current densities of the devices. The morphologies of the perovskites were analyzed through FE-SEM (JEOL JSM 6701F). Grazing-incidence wide-angle X-ray spectroscopy (GIWAXS) was performed using a Philips Panalytical-x\\u2019PertPROMRD instrument; the incident beam angle was above the critical angle (ca. 0.5\\u00b0). TRPL spectra were recorded using a time-correlated single photon counting spectrometer (WELLS-001 FX, DongWoo Optron). The pulse laser had a wavelength of 440\\u202fnm and an average power of 1 mW; it was operated with a duration of excitation of 2\\u202f\\u03bcs. XPS was performed using a ULVAC-PHI PHI 5000 Versaprobe II spectrometer and a monochromatic Al K\\u03b1 source. WFs were calculated using an incident light energy of 21.2\\u202feV [He(I) emission]. The samples were biased at \\u20135 V dc to drive low-energy secondary electrons into the detector.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: NiO-c,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Hydrochloric acid (HCl; 37% AR.), chlorobenzene (AR.) and N,N-Dimethylformamide (DMF; AR.) were obtained from RCI Labscan. Isopropanol (anhydrous, \\u226599.5%), lead (II) iodide (PbI2; 99%), were obtained from Sigma-Aldrich. PEDOT:PSS and PC60BM (PCBM; 99.0%) were obtained from Ossila. Methylammonium iodide (MAI; CH3NH3I) was obtained from Dyesol. All the materials were directly used without further purification.\\n\\nPerovskite solar cells based on p-i-n heterojunction structure of FTO/PEDOT:PSS/CH3NH3PbI3/PCBM/Ag were studied. FTO substrate was patterned by an equal volumetric mixtures of HCl:deionized (DI) water with Zn metal. The patterned FTO was cleaned under sonicator with detergent, DI water, acetone and isopropanol for 15\\u00a0min each, respectively, and dried with flowing N2. A hole transport materials (HTMs) was prepared from a mixtures of PEDOT:PSS and methanol with a volumetric ratio of 1:2, respectively. The mixed solution was sonicated for 30\\u00a0min in ambient condition. The PEDOT:PSS solution was spin-coated on the patterned FTO at 3000\\u00a0rpm for 60\\u00a0s. After the spin-coating, the PEDOT:PSS-coated FTO was annealed at 150\\u00a0\\u00b0C for 15\\u00a0min, cooling down to room temperature and transfer to a low relative humidity (<20%) grove box. CH3NH3PbI3 was formed using two-step spin-coating deposition process. For PbI2 layer deposition, PbI2 solution was prepared by dissolving 1\\u00a0M PbI2 in DMF. The solution was stirred at 70\\u00a0\\u00b0C. Before the deposition, the PEDOT:PSS films was pre-heated at 70\\u00a0\\u00b0C for 15\\u00a0min. Next, 120\\u00a0\\u03bcl of the PbI2 solution was spin-coated on the PEDOT:PSS films at 3000\\u00a0rpm for 30\\u00a0s, and immediately annealed at 70\\u00a0\\u00b0C for 15\\u00a0min. After cooling down, 120\\u00a0\\u03bcl of MAI solution was deposited on the PbI2 films with spin-coating rate of 2000\\u00a0rpm for 30\\u00a0s and annealed at 100\\u00a0\\u00b0C for 2\\u00a0h under flowing N2 gas to form CH3NH3PbI3 films. The MAI solution was prepared by dissolving 50\\u00a0mg/ml MAI in isopropanol and maintained by stirring at room temperature. For PCBM preparation, PCBM solution was prepared by dissolving PCBM in chlorobenzene with concentration of 20, 30, 40 and 50\\u00a0mg/ml. Two sets of PCBM solution was separated stirring at room temperature (non-heat) and 70\\u00a0\\u00b0C (pre-heat) for 12\\u00a0h. The non- and pre-heat PCBM solutions were deposited by spin-coating on the CH3NH3PbI3 films at 2000\\u00a0rpm for 30\\u00a0s. Finally, the Ag back contact was deposited on the PCBM layer by thermal evaporation.\\nMorphology of deposited films was observed by field emission scanning electron microscopy (FE-SEM, JEOL JSM-6335F) operating at a voltage of 15.0\\u00a0kV. Photovoltaic characteristics were measured under standard simulated solar radiation of 100\\u00a0mW/cm2 (AM1.5).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF >> IPA,\\n Perovskite_deposition_procedure: Spin-coating >> Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 70.0 >> 100.0,\\n Perovskite_deposition_thermal_annealing_time: 15.0 >> 120.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"For polymerization, 0.2 M of pyrrole monomer (C4H5N, 0.67 ml, Sigma\\u2013Aldrich, \\u2a7e99.5%) was first dissolved in 50 ml of deionized (DI) water and was kept stirring for 30 min at the room temperature. Thereafter, the aqueous ammonium peroxysulphate ((NH4)2S2O8, 0.2 M, Sigma\\u2013Aldrich, \\u2a7e99.5%) was added drop wise to the reaction mixture, using peristaltic pump. After completion of the reaction, the obtained blue-green color precipitates were centrifuged at \\u223c4000 rpm for 10 min. The final product was washed with copious amount of DI water, methanol and dried in vacuum oven at \\u223c40 \\u00b0C for 24 h [17].\\n\\nMethylamine (27.86 ml, CH3NH2, 40% in methanol, TCI chemicals) and hydroiodic acid (30 ml of 57 wt% in water, HI, Aldrich, 99%) were used to synthesize methylammonium iodide (CH3NH3I), as reported elsewhere [18]. In brief, the reaction mixture of CH3NH2 and HI was placed in a chiller and maintained at 0 \\u00b0C for 4 h to obtain precipitates which were recovered by the evaporation at 50 \\u00b0C for 1 h. The final yellow product of CH3NH3I was repeatedly washed with diethyl ether ((C2H5)2O Alfa Aesar, 99% assay) and dried at 60 \\u00b0C in vacuum oven for 24 h. For the synthesis of CH3NH3PbI3, an equimolar CH3NH3I, and lead iodide (PbI2, Aldrich, 99%) were dissolved in \\u03b3-butyrolactone (C4H6O2, TCI, 99%), and kept at 60 \\u00b0C for 12 h.\\n\\nFor the fabrication, PEDOT:PSS was first spin coated at \\u223c2000 rpm for 40 s on cleaned ITO-PET substrate, and annealed at 120 \\u00b0C for 10 min. Afterward, the synthesized perovskite (CH3NH3PbI3) solution was coated on annealed PEDOT:PSS/ITO-PET thin film through spin coating at the speed of \\u223c2000 rpm for 40 s with 0.45 \\u03bcm pore PVDF membrane syringe filter (Jet Biofil) at an ambient atmosphere. The obtained thin films were annealed at 100 \\u00b0C for 30 min to achieve CH3NH3PbI3/PEDOT:PSS/ITO-PET. Phenyl-C61-butyric acid methyl ester (PC61BM, 2 wt%) solution in chlorobenzene was coated at \\u223c1000 rpm to obtain PC61BM/CH3NH3PbI3/PEDOT:PSS/ITO-PET thin film. PPy solution in m-cresol (15 mg/1 ml) with 13.6 \\u03bcl Li-bis (trifluoromethanesulfonyl) imide (CF3SO2NLiSO2CF3, Li-TFSI, 28.3 mg/1 ml, TCI, >98%) and 6.8 \\u03bcl TBP (C9H13N, Aldrich, 96%) as additives was again spin-coated on PC61BM/CH3NH3PbI3/PEDOT:PSS/ITO-PET substrate at \\u223c3000 rpm for 30 s, and dried at 100 \\u00b0C for 15 min. Finally, Ag contacts (thickness \\u223c100 nm) were made by the thermal evaporation to achieve the flexible perovskite solar cell as Ag/PPy/PC61BM/CH3NH3PbI3/PEDOT:PSS/ITO-PET.\\n\\nThe atomic force spectroscopy (AFM, Nanoscope IV, Digital Instruments, Santa Barbara, USA) was used to investigate the morphology of PPy/PC61BM/CH3NH3PbI3/ITO-PET and CH3NH3PbI3/ITO-PET thin films. The confocal images of PPy/PC61BM/CH3NH3PbI3/ITO-PET and CH3NH3PbI3/ITO-PET thin films were characterized by Confocal Laser Scanning Microscope (LSM 510 META, Carl Zeiss, Germany). The crystalline nature and phases of PPy/PC61BM/CH3NH3PbI3/ITO-PET and CH3NH3PbI3/ITO-PET thin films were studied by X-ray powder diffraction (XRD, Rigaku, Cu K\\u03b1, \\u03bb = 1.54178 \\u00c5) in the Bragg angle ranging between 10\\u00b0 and 60\\u00b0 and the optical properties of the deposited thin film were demonstrated by UV\\u2013Vis spectrophotometer (JASCO, V-670, Japan). The current density (J)\\u2013voltage (V) measurements were performed for elucidating the performance of the flexible perovskite solar cell using computerized digital multimeter (model 2000, Keithley) with a variable load under one sun (1.5 AM at 100 mW/cm2). The simulated sunlight was supplied by using metal halide lamp of 1000 W and the light intensity was adjusted to \\u223c100 mW/cm2 (1.5 AM), using Si photo detector fitted with a Ka-5 filter as a reference (calibrated at NREL, USA). The incident photon-to-current conversion efficiency (IPCE) was carried out by a specially designed IPCE system for solar cell by PV measurements, Inc., USA. Before performing the IPCE measurements, the system was calibrated with a silicon photodiode, using the NIST-calibrated photodiode G425 as standard. The IPCE results of the flexible perovskite solar cell were collected as a function of wavelength from \\u223c400 to 800 nm using 75 W Xe lamp as a light source for generating monochromatic beam at a low chopping frequency. The charge collection efficiency and photoelectron density were revealed by using intensity-modulated photocurrent spectroscopy (IMPS) and intensity-modulated photovoltage spectroscopy (IMVS) using IVIUM technologies (CompactStat.e20250, USA).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: PET | ITO,\\n ETL_stack_sequence: PCBM-60 | PPy,\\n ETL_additives_compounds: Unknown | Li-TFSI; TBP,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: GBL,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 30,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: TRUE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"MAI (Methyl ammonium iodide, 99.99%), PbI2 (99.9985%) were purchased and used as is to make precursors for MAPbI3 perovskites. DMF (Dimethylformamide, 99.5%), DMSO (Dimethyl sulfoxide, 99.8%), CBZ (chlorobenzene, mono, >\\u202f99.5%) were employed as main solvents and/or anti-solvents. For charge transport materials, poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT: PSS, PVP AI 4083) as a hole transport layer (HTL) and Phenyl-C61-butyric acid methyl ester (PCBM, 99.5%, Nano-C) as an electron transport layer (ETL) were used as is. In addition, NiOx precursor solution was made using Ni(NO3)2\\u00b76H2O (99.999%), ethyleneglycol (99.5%), and ethylenediamine (EDA, 99.0%).\\n\\nFor characterization of the solution processed NiOx HTL, it was coated on bare glass or ITO substrates. First, NiOx precursor solutions with various EDA additive concentration (0, 2.5, 5.0, 6.7, 7.5, 10.0\\u202fv/v %) were made by dissolving nickel nitrate hexahydrate (Ni(NO3)2\\u00b76H2O) of 0.291\\u202fg in ethyleneglycol of 1\\u202fmL. The solutions were stirred at room temperature for 12\\u202fh. The image of resultant solutions is shown in Fig. 1. The NiOx precursor solutions with various EDA concentration (0\\u201310.0%) were coated onto each substrate at 4000\\u202frpm for 90\\u202fs and annealed at 300\\u202f\\u00b0C for 60\\u202fmin in air-ambient.\\n\\nITO glass substrates (15\\u202f\\u03a9\\u00b7sq\\u22121) were cleaned with a sequential step of acetone, methyl alcohol, and isopropyl alcohol for 10\\u202fmin, respectively. After drying them in an oven, UV-ozone treatment for hydrophilic surfaces was made for 20\\u202fmin. Then PEDOT: PSS (PVP AI 4083) solution was spin-casted on the substrates at 4000\\u202frpm for 50\\u202fs and annealed at 140\\u202f\\u00b0C in air-ambient. Regarding perovskite precursor, MAPbI3 (50\\u202fwt%) perovskite solution was made by dissolving MAI (0.286\\u202fg) and PbI2 (0.830\\u202fg) 1\\u202fmL DMF with DMSO (128\\u202f\\u03bcL), and stirred at 65\\u202f\\u00b0C for 12\\u202fh. Afterward, MAPbI3 perovskite precursors (filtered with a 0.45\\u202f\\u00b5m PVDF filter) were spin-casted on the PEDOT: PSS or NiOx HTLs in a glovebox. And then, the PC61BM solution was spin-coated onto the perovskite films at 400\\u202frpm for 1\\u202fs and 1500\\u202frpm at 35\\u202fs in the glovebox too. Finally, silver electrode was thermally-evaporated under high vacuum through a shadow mask. The active area of solar cells was 4\\u202fmm2.\\n\\nOptical transmittance spectra of the various HTLs were characterized by ultraviolet-visible (UV\\u2013Vis) spectrophotometry (UV-2700; Shimadzu). Fourier transform infrared (FT-IR) measurement was performed to analyze film components by using the equipment (Vertex 80\\u202fv; Bruker) with a detector detector (mercury-cadmium-telluride: MCT) and a beam-splitter (KBr). The FT-IR was measured with scanning 128 times under a resolution of 2\\u202fcm\\u22121. The film thicknesses were measured by a surface profiler (D-100; KLA Tencor). Surface morphologies of the various NiOx HTLs were analyzed by using atomic force microscopy (AFM) (SA-AFM; Proves Inc.). Electrical resistivity of those NiOx films were estimated by preparing patterned Ag-electrodes on film surfaces, and following current-voltage sweeping was made with using a parameter analyzer. All current density-voltage (J-V) curves of the fabricated perovskite solar cells were measured by a solar simulator (Polaronix K201; McScience) under an AM 1.5 standard condition in air-ambient (100\\u202fmW/cm2, relative humidity =\\u202f20\\u201330%, 25\\u202f\\u00b0C).\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: Unknown,\\n Perovskite_deposition_thermal_annealing_time: Unknown,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.04,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"Methyl ammonium iodide (CH3NH3I) and lead iodide (PbI2) were purchased from Sigma Aldrich and stored in the inert atmosphere. Indium doped tin oxide (ITO) coated glass substrates were purchased from M/S Global Nanotech. Poly(3,4-ethylenedioxythiophene):polystyrene sulfonic acid (PEDOT:PSS) was obtained from Sigma Aldrich and stored in 30\\u202f\\u00b0C. All other solvents were obtained from Sigma-Aldrich (St. Louis, MO) and used as received. UV\\u2013Vis absorption of perovskite thin film was recorded with a Perkin Elmer lambda 950 UV\\u2013Vis spectrometer.\\nThe steady state photoluminescence spectra and time resolved photoluminescence spectra were recorded by exciting the samples with a 355\\u202fnm line of Nd:YAGlaser with pulse width of 840\\u202fps, repetition rate of 1000\\u202fHz, and power range 1\\u20135\\u202f\\u00b5W/cm2.The spectra were recorded using Andor i-Star gated i-CCD that has a minimum gate width of 700\\u202fps with variable gate-delay technique to get a intensity variation of over 4\\u20135 orders of magnitude. XRD pattern was recorded with (Bruker DA advanced XRD equipped with CuK\\u03b1 radiation at room temperature) using graphite monochromatic Cu K\\u03b1 radiation at a scanning rate of 0.1\\u00b0/s over the Bragg angle range of 5.0\\u00b0\\u201370.0\\u00b0 (2\\u03b8). The surface morphology and microstructures of the perovskite thin film was studied by FESEM instrument operated at accelerating voltage of 15\\u202fkV. The current density\\u2013voltage (J\\u2013V) characteristics of PSC devices were measured using a Keithley 2400 source measure unit.\\n\\nPrecursor solution of MAI was synthesized using previously reported method described elsewhere [21].The perovskite precursor solution was prepared by mixing equal molar ratio of MAI and PbI2 in polar solvent DMF. ITO coated glass substrates were patterned by wet etching utilizing Zn and HCl and subsequently cleaned with soap solution, DI water, ethanol, acetone and isopropanol respectively for 15\\u202fmin each followed by ozone treatment for 15\\u202fmin. PEDOT:PSS/deionized water (1:3 v/v) solution was filtered through 0.45\\u202f\\u00b5m filter and spin-coated at 4000\\u202frpm onto the patterned substrates for 50sec, the prepared thin film was then baked, at 150\\u202f\\u00b0C for 15\\u202fmin in air. Precursor solution (CH3NH3I/PbI2 in DMF) was spin coated at 3000\\u202frpm on PEDOT: PSS covered substrate for 30\\u202fs (under ambient condition). Subsequently, chlorobenzene solution (150\\u202f\\u00b5l) were dripped onto the substrate followed by annealing at 100\\u202f\\u00b0C for 10\\u202fmin to get more compact and larger grain size of perovskite crystal. The schematic of the method is shown Fig. 1 . The standard thermally annealed film was also prepared for comparison.\\n\\nThe prototype solar cells devices were prepared in p-i-n geometry in ITO/PEDOT:PSS/MAPbI3/C60/BCP/Al architecture. To prepare the devices a 30\\u202fnm layer of C60 and 5\\u202fnm thick layer of BCP was deposited at high vacuum conditions. The current density\\u2013voltage (J\\u2013V) characteristics of PSCs were measured using a Keithley 2400 source measure unit. The solar cell performance was characterized under illumination by an Air Mass 1.5 Global (AM 1.5 G) solar simulator with an irradiation intensity of 100 mW cm-2 scanning the devices in the range of \\u22122V to 1\\u202fV. Hysteresis of the device was tested by doing a forward and backward scan between \\u22122V and 1\\u202fV.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: C60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Evaporation | Evaporation,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Al,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All the reagents and reactants were purchased and used as received without further purification unless stated otherwise. Potassium t-butoxide (t-BuOK) was from Aladdin (China), PbI2, lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and 4-tert-butylpyridine (TBP) from Sigma\\u2013Aldrich, N,N-dimethylformamide (DMF) and chlorobenzene from Alfar Aesar, hydroiodic acid (AR, 45 wt% in water) and methylamine (AR, 27% in methanol) from Sinopharm Chemical Reagent Co. Ltd, respectively. Spiro-OMeTAD was from Luminescence Technology Corp., Taiwan. Other reagents (analytical grade) were purchased from Tianjin Guangfu Fine Chemical Research Institute. N,N\\u2032-di(p-tolyl)-N,N\\u2032-dipheny-1,1\\u2032-biphenyl-4,4\\u2032-diamine was from Tianjin Zhongmin Technology Co. Ltd (China), which was recrystallized from toluene before use. Tetrahydrofuran (THF), N,N-dimethylformamide (DMF) and phosphorus oxychloride (POCl3) were freshly distilled before use. Methyl ammonium iodide (CH3NH3I) was synthesized by following the literature . Substrates were fluorine-doped tin oxide conducting glass (FTO, Pilkington, sheet resistance: 14 \\u03a9 square\\u22121, thickness: 2.2 mm). Patterned FTO glass was first cleaned with mild detergent, subsequently rinsed with distilled water for several times and with ethanol in an ultrasonic bath, and finally dried under air stream.\\n\\nSynthetic routes for the HTMs are shown in Scheme 1 . [p-(di-p-tolylamino)phenyl]triphenylphosphonium bromide (3.14 g, 5.00 mmol) and 2-formyl-thiophene (0.28 mL, 3.00 mmol) or 3-formyl-N-ethyl-carbazole (0.71 mL, 3.00 mmol) were mixed in anhydrous THF (40 mL) and stirred at ambient temperature under the protection of N2 atmosphere for 15 min. Subsequently, t-BuOK (1.68 g, 15.00 mmol) in anhydrous THF (20 mL) was added dropwise, which was stirred overnight. The reaction mixture was quenched with water, then extracted with CH2Cl2 for three times (100 mL \\u00d7 3). The combined extracts were dried over anhydrous Na2SO4 and subsequently filtered to remove the desiccant. Solvents were removed by rotary evaporation, then separated over a silica gel column with petroleum ether/ethylacetate (VPE/VEA, 5/1) as eluent to afford light yellow solids, defined as apv-T and apv-EC, respectively. The two HTMs are fully characterized by 1H/13C NMR spectrometry, mass spectrometry, IR spectrometry as follows.\\nFor apv-T, Mp: 148\\u2013149 \\u00b0C; 1H NMR (CDCl3, ppm): 2.35 (s, 6H), 6.873 (s, 1H), 6.905 (s, 1H), (d, 2H, J= 8.4 Hz), 6.994\\u223c7.039 (m, 8H), 7.058 (d, 2H, J= 8 Hz), 7.132 (s, 1H), 7.174 (d, 2H, J = 4.5 Hz), 7.284 (s, 1H), 7.32 (d, 2H, J= 8.5 Hz); 13C NMR (500 MHz, CDCl3) \\u03b4 (ppm): 147.8, 145.1, 143.44, 132.77, 130.16, 129.91, 128.11, 127.53, 127.03, 125.28, 124.80, 123.66, 122.29, 119.68, 20.82; HRMS (APCI): found: m/z 382.1626 (M+), Calcd for C26H23NS: M+H, 382.26; IR (cm\\u22121, KBr): 3018 (\\u03bdC\\u2212H(thiophene)), 2914, 2854 (\\u03bdC\\u2212H( CH3)), 1595 (\\u03bdC=C( HC CH )), 1500 (\\u03bdC=C, phenyl), 1319 (\\u03b4C\\u2212H), 948 (\\u03b4C\\u2212H, ( HC CH )), 817 (\\u03b4C\\u2212H, substituted phenyl), 698 (\\u03b4C\\u2212H, thiophene).\\nFor apv-EC, Mp: 114\\u2013116 \\u00b0C; 1H NMR (500 MHz, CDCl3) \\u03b4 (ppm): 1.425-1.453 (t, 3H), 2.321 (s, 6H), 4.344\\u20134.387 (q, 2H), 7.011\\u20137.028 (d, 6H, J= 8.5 Hz), 7.066-7.102 (m, 5H) 7.175\\u20137.236 (m, 2H), 7.364\\u20137.406 (m, 4H), 7.453\\u20137.484 (t, 1H), 7.644\\u20137.661 (d, 1H, J= 8.5 Hz), 8.112\\u20138.128 (d, 1H, J = 8.0 Hz), 8.200 (s, 1H); 13C NMR (500 MHz, CDCl3) \\u03b4 (ppm): 13.87, 20.84, 37.66, 108.62, 118.43, 119.01, 120.51, 122.80, 124.30, 124.60, 125.69, 126.91, 127.68, 128.99, 129.89, 131.50, 132.50, 139.54, 140.37, 145.27, 147.26; HRMS (APCI): Found: m/z 493.2641 (M+), calcd for C36H32N2: M+H, 493.27; IR (cm\\u22121, KBr): 2928 (\\u03bdC\\u2212H( NCH3)), 2851 (\\u03bdC\\u2212H( CH3)), 1599 (\\u03bdC=C ( HC=CH )), 1506 (\\u03bdC=C, phenyl), 1322 (\\u03b4C\\u2212H), 969 (\\u03b4C-H, ( HC CH )), 813 (\\u03b4C\\u2212H, substituted phenyl).\\n\\n1H and 13C NMR (500 MHz, CDCl3) spectra were conducted on a Bruker AVIII500 with tetramethylsilane (TMS) as reference at 298 K. High resolution mass spectra (HR-MS) were obtained on a Bruker Micro TOF-Q II APCI-quadrupole-os-TOF tandem mass spectrometer. UV-visible absorption spectra of the HTMs in dichloromethane solutions (1 \\u00d7 10\\u22125 M) were measured on Shimadzu UV-2550. FT-IR spectra were obtained on a NICOLET380 (Thermo Nicolet, USA) with KBr pellets. Ultraviolet photoelectron spectra (UPS) were carried out on Sumitomo Heavy Industries, PYS-202. Differential scanning calorimetry (DSC) was performed on PerkinElmer DSC8000 at a heating rate of 20 \\u00b0C min\\u22121 under N2 atmosphere. Time-of-flight (TOF) measurements were carried out on TOF401 (Sumitomo Heavy Industries. Ltd., Japan). For TOF measurement, samples with ITO/HTM/Al structure were prepared by using vacuum deposition method with about 1 \\u03bcm-thickness HTM layer and 150 nm-thickness Al film in an active area of 3 \\u00d7 10 mm2. The film thickness was obtained by using a surface profiler (KLA-Tencor, P-6). The morphology of the cells was determined by scanning electron microscope (SEM, FEI XL30S-FEG).\\n\\nA 30 nm-thickness TiO2 compact underlayer was spin-coated on the pre-cleaned FTO glass, then sintered at 500 \\u00b0C. A 500 nm-thickness mesoporous TiO2 films were screen-printed on the top of compact TiO2 layer by using lab-made pastes consisting of 20 nm anatase TiO2 nanoparticles according to the reference . The films were dried at 80 \\u00b0C for 30 min, then sintered at 450 \\u00b0C for 30 min, subsequently treated with 25 mM TiCl4 aqueous solution at 70 \\u00b0C for 40 min, and finally sintered at 500 \\u00b0C for 30 min.\\nCH3NH3PbI3 layer was deposited by using a modified two-step deposition method according to our previous work . First, PbI2/TiO2 films were obtained in a dry box filled with nitrogen, briefly, 1.2 M PbI2 solution in DMF was spin-coated on mesoporous TiO2 films at 3000 rpm for 60 s, then heated at 90 \\u00b0C for 5 min. The films were subsequently immersed into isopropanolic solution of CH3NH3I (10 mg mL\\u22121) under ambient environment with the humidity of less than 20% at room temperature . The whole immersion time to keep the full conversion from PbI2 to CH3NH3PbI3 is 120 min. The color of the samples changed into dark brown, then rinsed with isopropanol thoroughly, finally heated at 90 \\u00b0C for 40 min. HTM chlorobenzene solutions with a concentration of 20 mg mL\\u22121 were spin-coated at 3000 rpm for 20 s on the top of CH3NH3PbI3 layer. Finally, 80 nm-thickness Au electrode was thermally evaporated under the vacuum of 10\\u22127 Torr.\\n\\nFor J\\u2013V characteristics, the cells were illuminated under 100 mW cm\\u22122 (AM 1.5) by an Oriel solar simulator 91160A calibrated with a standard Si reference cell (National Institute of Metrology, China), while the data were recorded on Princeton Applied Research, Model 263A. The current-voltage scans at a sweep rate of 80 mV s\\u22121, starting from short circuit to forward bias (forward) and back from forward bias to short circuit (backward). Total 100 data points were collected with the dwell time of 0.13 s per point. A mask with a window of 0.08 cm2 was used to define the active area of the cell. The monochromatic incident photon-to-electron conversion efficiency (IPCE) spectrum was obtained on a lab-made IPCE testing system . Time-resolved photoluminescence (PL) spectra was obtained on a PL Spectrometer (Edinburgh Instruments, FLS 900), excited with a picosecond pulsed diode laser (EPL-445), and measured at 775 nm after excitation at 445 nm. Electrochemical impedance spectra (EIS) were performed on a ZAHNER IM6e electrochemical workstation in the dark at the applied bias voltage from 400 to 900 mV with a perturbation amplitude of 10 mV in the frequency range from 0.1 to 105 Hz. The obtained EIS spectra were fitted by Zview software based on appropriate equivalent circuit. For stability testing, the perovskite solar cells were kept in the desiccator with the humidity of about 20% in the dark for 15 days and tested once every two days.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | FTO,\\n ETL_stack_sequence: TiO2-c | TiO2-mp,\\n ETL_additives_compounds: Unknown | TiCl4,\\n ETL_deposition_procedure: Spin-coating | Screen printing,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating >> CBD,\\n Perovskite_deposition_thermal_annealing_temperature: 90.0 >> 90.0,\\n Perovskite_deposition_thermal_annealing_time: 5.0 >> 40.0,\\n HTL_stack_sequence: apv-T,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Au,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.08,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: nip,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"After clean the ITO coated glass substrates (Samsung Corning Co.) with detergent and deionized water (DI) water, sonication in DI water, acetone, and isopropanol was carried out sequentially. Before the preparation of HTLs, substrates were treated with UV/O3 plasma for 20\\u202fmin to make hydrophilic surface. Conventional PEDOT: PSS and sol-gel derived NiOx was used as HTLs to find the effect of HTLs on performance and stability. Commercialized PEDOT:PSS (Heraeus, CleviosTM P VP AI 4083) was spin-coated by two-step (at 500\\u202frpm for 5\\u202fs and 5000\\u202frpm for 40\\u202fs) and annealed at 120\\u202f\\u00b0C for 10\\u202fmin in air. For the sol-gel derive NiOx HTLs, 0.1\\u202fM nickel acetate (Sigma-Aldrich) mixed in ethanol with 6\\u202fvol % ethanolamine was spin-coated at 3000\\u202frpm for 40\\u202fs using precursor solution followed by annealing at 350\\u202f\\u00b0C for 30\\u202fmin in air. Then, the perovskite layer was spin-coated at 500\\u202frpm for 5\\u202fs and 5000\\u202frpm for 45\\u202fs using 35\\u202fwt% solution of CH3NH3I and PbI2 with a 1:1\\u202fM ratio in N, N-dimethylmethanamide (DMF) in a glove box filled with N2. During the second step of spin-coating process, 0.7\\u202fml toluene was dropped to obtain high quality perovskite films. Thermal annealing was performed at 100\\u202f\\u00b0C for 10\\u202fmin. The PCBM solution (20\\u202fmg PCBM in 1\\u202fml chlorobenzene) was spin-coated at 1000\\u202frpm for 60\\u202fs on perovskite films. To modify the interface of PCBM/semitransparent metal layer, 0.5\\u202fwt% PEIE in methanol was spin-coated at 5000\\u202frpm for 40\\u202fs. Finally, Cu (8\\u202fnm) and Ag (8\\u202fnm) were thermally evaporated as top metal electrodes, respectively, in vacuum of 10 \\u22126\\u202fTorr.\\nOptical transparency and electrical conductivity of thin metal top electrodes were characterized by using UV\\u2013vis spectrophotometer (Varian AU/DMS-100S) and 4-point-probe measurement (FPP-RS9, Dasol Eng.). Valence bands (VBs) of PEDOT:PSS and NiOx HTLs were measured using ultraviolet photoelectron spectroscopy (UPS, ESCALAB 210) with a He I (21.2\\u202feV) source. The photocurrent density-voltage (J-V) curves were obtained using a Keithley 2400 under the condition of 100\\u202fmW/cm2 illumination and AM 1.5\\u202fG condition after calibration of light intensity with certified reference silicon solar cell. To study performance deviation in a batch, 4 devices were fabricated in each condition and characterized. Statistics analysis was performed by characterizing 28 devices for each condition. Also, change in performance with exposure time in atmospheric condition was recorded without any encapsulation (samples are kept in atmospheric condition, not under the continuous illumination). Field-emission scanning electron microscopy (FE-SEM, HITACHI-SU8220) was used to observe device structure after stability test.\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 100,\\n Perovskite_deposition_thermal_annealing_time: 10,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Cu,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.1,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: TRUE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}, {\"instruction\": \"Summarize stack and method information from given paragraph about solar cell.\", \"input\": \"All solvents and chemicals were purchased and utilized as obtained. PEDOT:PSS (CLEVIOS PH 1000 suspension) was purchased from Heraeus. [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) and bathocuproine (BCP) were purchased from Sigma-Aldrich Co. LLC. CH3NH3PbI3-DMF (MAPbI3-DMF) was purchased from TCI Co., Ltd. All solvents and reagents were of the highest quality available and were used as received.\\n\\nThe F-doped tin oxides (FTO) glass (NSG-Pilkington, 15\\u202f\\u03a9/ square) and the indium-tin oxides (ITO) glass substrates (Geomatec Co., Ltd., 15\\u202f\\u03a9/ square) were cleaned ultrasonically with detergent, distilled water, and ethanol respectively, and treated with UV/O3 for 15\\u202fmin to eliminate organic impurities and make the surface clean. The PEDOT:PSS solution (CLEVIOS PH 1000 suspension) was diluted in isopropanol (IPA) (PEDOT:PSS solution : IPA\\u202f=\\u202f1:3 (v/v)). This solution was filtered, dropped 100\\u202f\\u03bcL on the substrate, and spin-coated at 1000\\u202frpm for 20\\u202fs. Finally, it was dried at 120\\u202f\\u00b0C for 5\\u202fmin to prepare the PEDOT:PSS layer.\\n\\nInverted perovskite solar cells consisting of\\u202f<\\u202fITO/PEDOT:PSS/MAPbI3/PCBM/ BCP/Ag\\u202f>\\u202for\\u202f<\\u202fFTO/PEDOT:PSS/MAPbI3/PCBM/BCP/Ag\\u202f>\\u202fwere fabricated. Details of the basic perovskite layer fabrication process have been described previously. [,]. A solution of CH3NH3PbI3-DMF (1.8\\u202fmol/L) in DMSO was spin-coated on PEDOT:PSS layer with 1000\\u202frpm for 10\\u202fs and with 5000\\u202frpm for 30\\u202fs, subsequently, inside a N2-filled glove box. During the spin coating, toluene was dripped on the perovskite layer. The film was annealed at 60\\u202f\\u00b0C for 10\\u202fmin and at 100\\u202f\\u00b0C for 10\\u202fmin, subsequently. The Electron transport layer was prepared by spin-coating of 50\\u202f\\u03bcL PCBM in chlorobenzene (20\\u202fmg/mL) on top of the perovskite films with 1000\\u202frpm for 60\\u202fs. Subsequently, a solution of 50\\u202f\\u03bcL BCP (1.0\\u202fmg/mL in methanol, which passed a 0.45\\u202f\\u03bcm cellulose acetate membrane filter tip beforehand) was spin-coated at 1000\\u202frpm for 60\\u202fs. Finally, Ag layer was coated by thermal evaporation as the back-contact electrodes.\\n\\nThe sheet resistance was characterized using a four-pin probe method (Loresta-EP MCP-T360, Mitsubishi Chemical Analytech Co., Ltd., the working range: 10\\u22122 and 106\\u202f\\u03a9/sq). The ionization potentials were obtained using AC-3 (Riken Keiki Co., Ltd.). The surface morphology was observed by SPA400 and SPI3800\\u202fN AFM (Seiko Instruments Inc.) in tapping mode. UV\\u2013vis spectra were determined on JASCO V-650 (JASCO Corp.). The photocurrent-voltage (J-V) characteristics of the PSCs were measured on a B2901\\u202fA (Agilent Technologies Inc.) source meter under irradiation of AM 1.5, 100\\u202fmW/cm2 (1 sun) supplied by a solar simulator (YSS-80, Yamashita Denso Co., Ltd.). Incident photon to current conversion efficiency (IPCE) spectrum was recorded on an IPCE system (CEP-2000, Bunkoukeiki Co., Ltd) under DC mode. Similarly, the excitation light intensity is calibrated by a Si photodiode. The incident light intensity was calibrated with a reference Si solar cell (BS-500BK, Bunkoukeiki Co., Ltd.). The active areas of the solar cells were regulated by a shadowing black mask with 0.3\\u202fcm\\u202f\\u00d7\\u202f0.3\\u202fcm opening.\\n\\n\", \"output\": \"<s> Substrate_stack_sequence: SLG | ITO,\\n ETL_stack_sequence: PCBM-60 | BCP,\\n ETL_additives_compounds: Unknown,\\n ETL_deposition_procedure: Spin-coating | Spin-coating,\\n Perovskite_composition_long_form: MAPbI3,\\n Perovskite_composition_short_form: MAPbI,\\n Perovskite_additives_compounds: ,\\n Perovskite_deposition_solvents: DMF; DMSO,\\n Perovskite_deposition_procedure: Spin-coating,\\n Perovskite_deposition_thermal_annealing_temperature: 60; 100,\\n Perovskite_deposition_thermal_annealing_time: 10.0; 10.0,\\n HTL_stack_sequence: PEDOT:PSS,\\n HTL_additives_compounds: ,\\n HTL_deposition_procedure: Spin-coating,\\n Backcontact_stack_sequence: Ag,\\n Backcontact_additives_compounds: ,\\n Backcontact_deposition_procedure: Evaporation,\\n Stability_measured: FALSE,\\n Stability_average_over_n_number_of_cells: 1,\\n Stability_temperature_range: nan; nan,\\n Stability_atmosphere: Unknown,\\n Stability_time_total_exposure: ,\\n Stability_PCE_initial_value: ,\\n Stability_PCE_end_of_experiment: ,\\n Cell_area_measured: 0.09,\\n Cell_number_of_cells_per_substrate: 0,\\n Cell_architecture: pin,\\n Cell_flexible: FALSE,\\n Cell_semitransparent: FALSE,\\n Cell_semitransparent_wavelength_range: nan; nan,\\n Module: FALSE</s>\"}]"
  },
  {
    "path": "SII_MDP/regression_evaluate.py",
    "content": "import numpy as np\r\nfrom sklearn.metrics import classification_report\r\nfrom sklearn.metrics import confusion_matrix\r\nimport matplotlib.pyplot as plt\r\n\r\n\r\ndef test_regression():\r\n    voc = []\r\n    voc_hat = []\r\n    jsc = []\r\n    jsc_hat = []\r\n    pce = []\r\n    pce_hat = []\r\n\r\n    f = open(\"C:\\\\Users\\\\94833\\\\Desktop\\\\regression40_382_90output.txt\", encoding=\"utf-8\")\r\n    lines = f.readlines()\r\n    line_index = 0\r\n    output_list = []\r\n    answer_list = []\r\n\r\n    output_text = ''\r\n    answer_text = ''\r\n    for line in lines:\r\n        if line_index % 27 == 19:\r\n            output_text = str(line)\r\n        elif line_index % 27 == 20:\r\n            output_text = output_text + str(line)\r\n        elif line_index % 27 == 22:\r\n            output_text = output_text + str(line).split(\"@\")[0]\r\n            output_list.append(output_text)\r\n        elif line_index % 27 == 23:\r\n            answer_text = str(line).split(\"->\")[1]\r\n        elif line_index % 27 == 24:\r\n            answer_text = answer_text + str(line)\r\n        elif line_index % 27 == 26:\r\n            answer_text = answer_text + str(line).split(\"@\")[0]\r\n            answer_list.append(answer_text)\r\n        line_index = line_index + 1\r\n\r\n    print(output_list)\r\n    print(answer_list)\r\n\r\n    for i in range(len(answer_list)):\r\n        print(\"answer list len: \" + str(len(answer_list)))\r\n        print(\"output list len: \" + str(len(output_list)))\r\n        answers = answer_list[i].split(\"\\n\")\r\n        results = output_list[i].split(\"\\n\")\r\n        if len(answers) != len(results):\r\n            print(\"schema(s) missing\")\r\n            continue\r\n        for schema_i in range(len(results)):\r\n            answer_schema = answers[schema_i].split(\":\")[0].strip()\r\n            result_schema = results[schema_i].split(\":\")[0].strip()\r\n            \"\"\"\r\n            if answer_schema != result_schema:\r\n                print(\"schema unaligned:\" + answer_schema + \" <> \" + result_schema)\r\n                continue\r\n            \"\"\"\r\n\r\n            schema_answer = answers[schema_i].split(\":\")[-1].strip()\r\n            schema_result = results[schema_i].split(\":\")[-1].strip()\r\n\r\n            answer_figure = float(schema_answer)\r\n            result_figure = float(schema_result)\r\n\r\n            # result_schema == \"JV default Voc\":\r\n            if \"Voc\" in result_schema:\r\n                voc.append(answer_figure)\r\n                voc_hat.append(result_figure)\r\n\r\n            # result_schema == \"JV default Jsc\":\r\n            elif \"Jsc\" in result_schema:\r\n                jsc.append(answer_figure)\r\n                jsc_hat.append(result_figure)\r\n\r\n            # result_schema == \"JV default PCE\":\r\n            elif \"PCE\" in result_schema:\r\n                pce.append(answer_figure)\r\n                pce_hat.append(result_figure)\r\n                print(\"answer: \" + str(answer_figure))\r\n                print(\"result: \" + str(result_figure))\r\n\r\n        print(\"______________________________\")\r\n\r\n    mae_voc = np.mean(np.abs(np.array(voc) - np.array(voc_hat)))\r\n    mae_jsc = np.mean(np.abs(np.array(jsc) - np.array(jsc_hat)))\r\n    mae_pce = np.mean(np.abs(np.array(pce)-np.array(pce_hat)))\r\n    print(\"mae_voc: \" + str(mae_voc))\r\n    print(\"mae_jsc: \" + str(mae_jsc))\r\n    print(\"mae_pce: \" + str(mae_pce))\r\n    print(\"______________________________\")\r\n\r\n    rmse_voc = np.sqrt(np.mean(np.square(np.array(voc) - np.array(voc_hat))))\r\n    rmse_jsc = np.sqrt(np.mean(np.square(np.array(jsc) - np.array(jsc_hat))))\r\n    rmse_pce = np.sqrt(np.mean(np.square(np.array(pce) - np.array(pce_hat))))\r\n    print(\"rmse_voc: \" + str(rmse_voc))\r\n    print(\"rmse_jsc: \" + str(rmse_jsc))\r\n    print(\"rmse_pce: \" + str(rmse_pce))\r\n    print(\"______________________________\")\r\n\r\n    mean_voc = np.mean(voc)\r\n    mean_jsc = np.mean(jsc)\r\n    mean_pce = np.mean(pce)\r\n    print(\"mean_voc: \" + str(mean_voc))\r\n    print(\"mean_jsc: \" + str(mean_jsc))\r\n    print(\"mean_pce: \" + str(mean_pce))\r\n    print(\"______________________________\")\r\n\r\n    var_voc = np.var(voc)\r\n    var_jsc = np.var(jsc)\r\n    var_pce = np.var(pce)\r\n    print(\"var_voc: \" + str(var_voc))\r\n    print(\"var_jsc: \" + str(var_jsc))\r\n    print(\"var_pce: \" + str(var_pce))\r\n    print(\"______________________________\")\r\n\r\n\r\ndef draw_regression():\r\n    voc = []\r\n    voc_hat = []\r\n    jsc = []\r\n    jsc_hat = []\r\n    pce = []\r\n    pce_hat = []\r\n\r\n    f = open(\"C:\\\\Users\\\\94833\\\\Desktop\\\\regression40_382_output.txt\", encoding=\"utf-8\")\r\n    lines = f.readlines()\r\n    line_index = 0\r\n    output_list = []\r\n    answer_list = []\r\n\r\n    output_text = ''\r\n    answer_text = ''\r\n    for line in lines:\r\n        if line_index % 26 == 18:\r\n            output_text = str(line).split(\"###\")[1]\r\n        elif line_index % 26 == 19:\r\n            output_text = output_text + str(line)\r\n        elif line_index % 26 == 21:\r\n            output_text = output_text + str(line).split(\"@\")[0]\r\n            output_list.append(output_text)\r\n        elif line_index % 26 == 22:\r\n            answer_text = str(line).split(\"->\")[1]\r\n        elif line_index % 26 == 23:\r\n            answer_text = answer_text + str(line)\r\n        elif line_index % 26 == 25:\r\n            answer_text = answer_text + str(line).split(\"@\")[0]\r\n            answer_list.append(answer_text)\r\n        line_index = line_index + 1\r\n\r\n    print(output_list)\r\n    print(answer_list)\r\n\r\n    for i in range(len(answer_list)):\r\n        answers = answer_list[i].split(\"\\n\")\r\n        results = output_list[i].split(\"\\n\")\r\n        if len(answers) != len(results):\r\n            print(\"schema(s) missing\")\r\n            continue\r\n        for schema_i in range(len(results)):\r\n            answer_schema = answers[schema_i].split(\":\")[0].strip()\r\n            result_schema = results[schema_i].split(\":\")[0].strip()\r\n            \"\"\"\r\n            if answer_schema != result_schema:\r\n                print(\"schema unaligned:\" + answer_schema + \" <> \" + result_schema)\r\n                continue\r\n            \"\"\"\r\n\r\n            schema_answer = answers[schema_i].split(\":\")[1].strip()\r\n            schema_result = results[schema_i].split(\":\")[1].strip()\r\n\r\n            answer_figure = float(schema_answer)\r\n            result_figure = float(schema_result)\r\n\r\n            # result_schema == \"JV default Voc\":\r\n            if \"Voc\" in result_schema:\r\n                voc.append(answer_figure)\r\n                voc_hat.append(result_figure)\r\n\r\n            # result_schema == \"JV default Jsc\":\r\n            elif \"Jsc\" in result_schema:\r\n                jsc.append(answer_figure)\r\n                jsc_hat.append(result_figure)\r\n\r\n            # result_schema == \"JV default PCE\":\r\n            elif \"PCE\" in result_schema:\r\n                pce.append(answer_figure)\r\n                pce_hat.append(result_figure)\r\n                print(\"answer: \" + str(answer_figure))\r\n                print(\"result: \" + str(result_figure))\r\n\r\n        print(\"______________________________\")\r\n\r\n    plt.figure(figsize=(10.5, 3.5))\r\n    plt.subplot(131)\r\n    x_voc = np.array(voc)\r\n    y_voc = np.array(voc_hat)\r\n    plt.xlim(0.5, 1.2)\r\n    plt.ylim(0.5, 1.2)\r\n    x = np.linspace(0.5, 1.2, 50)\r\n    y = x\r\n    plt.plot(x_voc, y_voc, 'o')\r\n    plt.plot(x, y, color='green', linewidth=1.0, linestyle='--')\r\n    plt.xlabel(\"Experimental Voc (V)\")\r\n    plt.ylabel(\"Predicted Voc (V)\")\r\n\r\n    plt.subplot(132)\r\n    x_jsc = np.array(jsc)\r\n    y_jsc = np.array(jsc_hat)\r\n    plt.xlim(5, 25)\r\n    plt.ylim(5, 25)\r\n    x = np.linspace(5, 25, 50)\r\n    y = x\r\n    plt.plot(x_jsc, y_jsc, 'o')\r\n    plt.plot(x, y, color='green', linewidth=1.0, linestyle='--')\r\n    plt.xlabel(\"Experimental Jsc (mA/cm$^2$)\")\r\n    plt.ylabel(\"Predicted Jsc (mA/cm$^2$)\")\r\n\r\n    plt.subplot(133)\r\n    x_pce = np.array(pce)\r\n    y_pce = np.array(pce_hat)\r\n    plt.xlim(0, 20)\r\n    plt.ylim(0, 20)\r\n    x = np.linspace(0, 20, 50)\r\n    y = x\r\n    plt.plot(x_pce, y_pce, 'o')\r\n    plt.plot(x, y, color='green', linewidth=1.0, linestyle='--')\r\n    plt.xlabel(\"Experimental PCE (%)\")\r\n    plt.ylabel(\"Predicted PCE (%)\")\r\n\r\n    plt.tight_layout()\r\n    plt.savefig(\"./regression.png\")\r\n    plt.show()\r\n\r\n\r\n\r\n#test_classification()\r\ntest_regression()\r\n#draw_regression()\r\n"
  },
  {
    "path": "SII_MDP/regression_test.py",
    "content": "import torch\r\nfrom transformers import LlamaTokenizer, LlamaForCausalLM, GenerationConfig\r\nimport json\r\nimport sys\r\n\r\n\r\nmodel_path = str(sys.argv[1])\r\ndata_path = str(sys.argv[2])\r\n\r\n\r\ndef generate_prompt(prompt_instruction, prompt_input):\r\n    return \"instruction: \" + str(prompt_instruction) + \", input: \" + str(prompt_input)\r\n\r\n \r\ndef generate_prediction(model_path,data_path):\r\n    #load the model\r\n    tokenizer = LlamaTokenizer.from_pretrained(model_path)\r\n    model = LlamaForCausalLM.from_pretrained(\r\n        model_path,\r\n        load_in_8bit=False,\r\n        torch_dtype=torch.float16,\r\n        device_map=\"auto\"\r\n    )\r\n    with open(data_path,'r') as f:\r\n        data = json.load(f)\r\n\r\n    instructions = []\r\n    true_output = []\r\n    pred_output = []\r\n    c = 0\r\n    print(len(data))\r\n    for i in data:\r\n        print(c)\r\n        c+=1\r\n        text = generate_prompt(i['instruction'], i['input'])\r\n        input_ids= tokenizer(text, return_tensors=\"pt\").input_ids.to(\"cuda\") \r\n        generated_ids = model.generate(\r\n            input_ids, \r\n            max_length=2048,\r\n            do_sample=True, \r\n            repetition_penalty=1.0, \r\n            temperature=0.8, \r\n            top_p=0.75, \r\n            top_k=40\r\n        )\r\n        output = tokenizer.decode(generated_ids[0])\r\n        true_value = i['output']\r\n        instructions.append(i['instruction'])\r\n        true_output.append(true_value)\r\n        pred_output.append(output)\r\n    return true_output,pred_output\r\n\r\n\r\ntrue_output,pred_output = generate_prediction(model_path,data_path)\r\noutput_name = data_path.replace('.json','')\r\nf = open(output_name+'_output.txt','w')\r\nfor line in range(len(pred_output)):\r\n    f.write(\"prediction -> \"+pred_output[line]+'\\n')\r\n    f.write(\"answer -> \"+true_output[line]+'\\n')\r\nf.close()\r\n"
  },
  {
    "path": "SII_MDP/sii_evaluate.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 37,\n   \"id\": \"f8133064\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"stage_1_schema = [\\n\",\n    \"'Substrate_stack_sequence',\\n\",\n    \"'ETL_stack_sequence',\\n\",\n    \"'ETL_additives_compounds',\\n\",\n    \"'ETL_deposition_procedure',\\n\",\n    \"'Perovskite_composition_long_form',\\n\",\n    \"'Perovskite_composition_short_form',\\n\",\n    \"'Perovskite_additives_compounds',\\n\",\n    \"'Perovskite_deposition_solvents',\\n\",\n    \"'Perovskite_deposition_procedure',\\n\",\n    \"'Perovskite_deposition_thermal_annealing_temperature',\\n\",\n    \"'Perovskite_deposition_thermal_annealing_time',\\n\",\n    \"'HTL_stack_sequence',\\n\",\n    \"'HTL_additives_compounds',\\n\",\n    \"'HTL_deposition_procedure',\\n\",\n    \"'Backcontact_stack_sequence',\\n\",\n    \"'Backcontact_additives_compounds',\\n\",\n    \"'Backcontact_deposition_procedure',\\n\",\n    \"'Stability_measured',\\n\",\n    \"'Stability_average_over_n_number_of_cells',\\n\",\n    \"'Stability_temperature_range',\\n\",\n    \"'Stability_atmosphere',\\n\",\n    \"'Stability_time_total_exposure',\\n\",\n    \"'Stability_PCE_initial_value',\\n\",\n    \"'Stability_PCE_end_of_experiment',\\n\",\n    \"'Cell_area_measured',\\n\",\n    \"'Cell_number_of_cells_per_substrate',\\n\",\n    \"'Cell_architecture',\\n\",\n    \"'Cell_flexible',\\n\",\n    \"'Cell_semitransparent',\\n\",\n    \"'Cell_semitransparent_wavelength_range',\\n\",\n    \"'Module'\\n\",\n    \"]\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 38,\n   \"id\": \"e4c1fd0f\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"a_set = ['Substrate_stack_sequence', \\n\",\n    \"         'ETL_stack_sequence',\\n\",\n    \"         'ETL_additives_compounds',\\n\",\n    \"         'Perovskite_composition_long_form', \\n\",\n    \"         'Perovskite_composition_short_form', \\n\",\n    \"         'Perovskite_additives_compounds',\\n\",\n    \"         'HTL_stack_sequence',\\n\",\n    \"         'HTL_additives_compounds', \\n\",\n    \"         'Backcontact_stack_sequence',\\n\",\n    \"         'Backcontact_additives_compounds']\\n\",\n    \"b_set = ['Cell_area_measured', \\n\",\n    \"         'Cell_number_of_cells_per_substrate', \\n\",\n    \"         'Cell_architecture', \\n\",\n    \"         'Cell_flexible', \\n\",\n    \"         'Cell_semitransparent', \\n\",\n    \"         'Cell_semitransparent_wavelength_range']\\n\",\n    \"c_set = ['ETL_deposition_procedure', \\n\",\n    \"         'HTL_deposition_procedure',\\n\",\n    \"         'Backcontact_deposition_procedure',\\n\",\n    \"         'Perovskite_deposition_procedure',\\n\",\n    \"         'Perovskite_deposition_solvents', \\n\",\n    \"         'Perovskite_deposition_thermal_annealing_temperature', \\n\",\n    \"         'Perovskite_deposition_thermal_annealing_time']\\n\",\n    \"d_set = ['Stability_measured', \\n\",\n    \"         'Stability_average_over_n_number_of_cells', \\n\",\n    \"         'Stability_temperature_range', \\n\",\n    \"         'Stability_atmosphere', \\n\",\n    \"         'Stability_time_total_exposure', \\n\",\n    \"         'Stability_PCE_initial_value', \\n\",\n    \"         'Stability_PCE_end_of_experiment']\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 39,\n   \"id\": \"bd900f80\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def if_float(num_str):\\n\",\n    \"    try:\\n\",\n    \"        float(num_str)\\n\",\n    \"        return True\\n\",\n    \"    except ValueError:\\n\",\n    \"        return False\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 40,\n   \"id\": \"2a27c26c\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def single_match(single_answer, single_prediction):\\n\",\n    \"    a_words = single_answer[1].replace('|',';').replace(':',';').replace('>>',';').replace('Spin-coating','spin-coated').split(';')\\n\",\n    \"    p_words = single_prediction[1].replace('|',';').replace(':',';').replace('>>',';').replace('Spin-coating','spin-coated').split(';')\\n\",\n    \"    a_words = [x.strip() for x in a_words]\\n\",\n    \"    p_words = [x.strip() for x in p_words]\\n\",\n    \"    # 在prediction里但不在answer里，则为fp\\n\",\n    \"    # 在answer里但不在prediction里，则为fn\\n\",\n    \"    # 都在则为tp\\n\",\n    \"    tp = []\\n\",\n    \"    fp = []\\n\",\n    \"    fn = []\\n\",\n    \"    if single_answer[0] in ['ETL_stack_sequence', 'HTL_stack_sequence', 'Substrate_stack_sequence']:\\n\",\n    \"        answerSet = set()\\n\",\n    \"        outputSet = set()\\n\",\n    \"        for answer in a_words:\\n\",\n    \"            for ap in answer.split(\\\"-\\\"):\\n\",\n    \"                answerSet.add(ap)\\n\",\n    \"        for output in p_words:\\n\",\n    \"            for op in output.split(\\\"-\\\"):\\n\",\n    \"                outputSet.add(op)\\n\",\n    \"        a_words = list(answerSet)\\n\",\n    \"        p_words = list(outputSet)\\n\",\n    \"    elif 'procedure' in single_answer[0] or single_answer[0] == 'Stability_atmosphere':\\n\",\n    \"        answerSet = set()\\n\",\n    \"        outputSet = set()\\n\",\n    \"        for answer in a_words:\\n\",\n    \"            answerSet.add(answer.lower())\\n\",\n    \"        for output in p_words:\\n\",\n    \"            outputSet.add(output.lower())\\n\",\n    \"        a_words = list(answerSet)\\n\",\n    \"        p_words = list(outputSet)\\n\",\n    \"    elif 'temperature' in single_answer[0] or 'time' in single_answer[0]:\\n\",\n    \"        answerSet = set()\\n\",\n    \"        outputSet = set()\\n\",\n    \"        for answer in a_words:\\n\",\n    \"            if answer != 'nan' and answer != '' and answer != 'Unknown':\\n\",\n    \"                answerSet.add(str(float(answer)))\\n\",\n    \"            else:\\n\",\n    \"                answerSet.add(answer)\\n\",\n    \"        for output in p_words:\\n\",\n    \"            if output != 'nan' and output!='' and output != 'Unknown':\\n\",\n    \"                outputSet.add(str(float(output)))\\n\",\n    \"            else:\\n\",\n    \"                outputSet.add(output)\\n\",\n    \"        a_words = list(answerSet)\\n\",\n    \"        p_words = list(outputSet)\\n\",\n    \"    tmp_predictions = p_words\\n\",\n    \"    if single_answer[0] in ['Perovskite_composition_long_form', 'Perovskite_composition_short_form']:\\n\",\n    \"        tmp = []\\n\",\n    \"        for p in p_words:\\n\",\n    \"            for aw in a_words:\\n\",\n    \"                if p == aw:\\n\",\n    \"                    tp.append(p)\\n\",\n    \"                else:\\n\",\n    \"                    answer_word_set = set(aw.strip())\\n\",\n    \"                    output_word_set = set(p.strip())\\n\",\n    \"                    if answer_word_set.issubset(output_word_set) or output_word_set.issubset(answer_word_set):\\n\",\n    \"                        tp.append(p)\\n\",\n    \"                        tmp.append(aw)\\n\",\n    \"                        tmp_predictions.remove(p)\\n\",\n    \"                        tmp_predictions.append(aw)\\n\",\n    \"        for p in p_words:\\n\",\n    \"            if p not in tp:\\n\",\n    \"                fp.append(p)\\n\",\n    \"        for aw in a_words:\\n\",\n    \"            if aw not in tmp and aw not in tp:\\n\",\n    \"                fn.append(aw)\\n\",\n    \"    else:\\n\",\n    \"        for p in p_words:\\n\",\n    \"            if p.strip() in a_words:\\n\",\n    \"                tp.append(p.strip())\\n\",\n    \"            else:\\n\",\n    \"                fp.append(p.strip())\\n\",\n    \"        for aw in a_words:\\n\",\n    \"            if aw.strip() not in p_words:\\n\",\n    \"                fn.append(aw.strip())\\n\",\n    \"    return [tp, fp, fn, a_words, tmp_predictions]\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 41,\n   \"id\": \"db39772f\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def calculate_metrics(tp, fp, fn, ac):\\n\",\n    \"    precision = tp / (tp + fp)\\n\",\n    \"    recall = tp / (tp + fn)\\n\",\n    \"    f1 = precision*recall*2/(precision+recall)\\n\",\n    \"    acc = tp/ac\\n\",\n    \"    return round(precision,4), round(recall,4), round(f1,4), round(acc,4)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 42,\n   \"id\": \"5a694dd9\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def relation(a1, a2, p1, p2):\\n\",\n    \"    aas = []\\n\",\n    \"    pps = []\\n\",\n    \"    for a1_ in a1:\\n\",\n    \"        for a2_ in a2:\\n\",\n    \"            aas.append((a1_, a2_))\\n\",\n    \"    for p1_ in p1:\\n\",\n    \"        for p2_ in p2:\\n\",\n    \"            pps.append((p1_, p2_))\\n\",\n    \"    tp = []\\n\",\n    \"    fp = []\\n\",\n    \"    fn = []\\n\",\n    \"    for pps_ in pps:\\n\",\n    \"        if pps_ in aas:\\n\",\n    \"            tp.append(pps_)\\n\",\n    \"        else:\\n\",\n    \"            fp.append(pps_)\\n\",\n    \"    for aas_ in aas:\\n\",\n    \"        if aas_ not in pps:\\n\",\n    \"            fn.append(aas_)\\n\",\n    \"    return [tp, fp, fn, aas]\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 43,\n   \"id\": \"2498287b\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def relation_2(a1, a2, a3, a4, p1, p2, p3, p4):\\n\",\n    \"    aas = []\\n\",\n    \"    pps = []\\n\",\n    \"    for a1_ in a1:\\n\",\n    \"        for a2_ in a2:\\n\",\n    \"            for a3_ in a3:\\n\",\n    \"                for a4_ in a4:\\n\",\n    \"                    aas.append((a1_, a2_, a3_, a4_))\\n\",\n    \"    for p1_ in p1:\\n\",\n    \"        for p2_ in p2:\\n\",\n    \"            for p3_ in p3:\\n\",\n    \"                for p4_ in p4:\\n\",\n    \"                    pps.append((p1_, p2_, p3_, p4_))\\n\",\n    \"    tp = []\\n\",\n    \"    fp = []\\n\",\n    \"    fn = []\\n\",\n    \"    for pps_ in pps:\\n\",\n    \"        if pps_ in aas:\\n\",\n    \"            tp.append(pps_)\\n\",\n    \"        else:\\n\",\n    \"            fp.append(pps_)\\n\",\n    \"    for aas_ in aas:\\n\",\n    \"        if aas_ not in pps:\\n\",\n    \"            fn.append(aas_)\\n\",\n    \"    return [tp, fp, fn, aas]\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 44,\n   \"id\": \"6ccca89f\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def metrics(answers, predictions):\\n\",\n    \"    keys = ['tp', 'fp', 'fn', 'ans', 'pre']\\n\",\n    \"    store = {'tp':{'total':0},'fp':{'total':0},'fn':{'total':0},'ans':{'total':0}, 'pre':{'total':0}}\\n\",\n    \"    metrics_dict = {}\\n\",\n    \"    for i, answer in enumerate(list(answers.items())):       \\n\",\n    \"        if answer[0] in predictions.keys():\\n\",\n    \"            acc_prediction = (answer[0], predictions[answer[0]])\\n\",\n    \"        else:\\n\",\n    \"            return None\\n\",\n    \"        # print(answer, acc_prediction[1])\\n\",\n    \"        metrics = single_match(answer, acc_prediction)\\n\",\n    \"        for idx in range(4):\\n\",\n    \"            store[keys[idx]]['total'] +=len(metrics[idx])\\n\",\n    \"        if answer[0] in a_set or answer[0] in b_set or answer[0] in c_set or answer[0] in d_set:\\n\",\n    \"        # if answer[0] in b_set:\\n\",\n    \"            for idx in range(5):\\n\",\n    \"                store[keys[idx]][answer[0]]=metrics[idx]\\n\",\n    \"    # information extraction      \\n\",\n    \"    metrics_dict['ie'] = calculate_metrics(store['tp']['total'], store['fp']['total'], store['fn']['total'], store['ans']['total'])\\n\",\n    \"    # relationship extraction: ab, ac, abc-d\\n\",\n    \"    ab_metrics = [0,0,0,0]\\n\",\n    \"    for a in a_set:\\n\",\n    \"        for b in b_set:\\n\",\n    \"            relations = relation(store['ans'][a], store['ans'][b], store['pre'][a], store['pre'][b])\\n\",\n    \"            for i in range(4):\\n\",\n    \"                ab_metrics[i] += len(relations[i])\\n\",\n    \"    metrics_dict['ab'] = calculate_metrics(ab_metrics[0], ab_metrics[1], ab_metrics[2], ab_metrics[3])\\n\",\n    \"    ac_metrics = [0,0,0,0]\\n\",\n    \"    for a in a_set:\\n\",\n    \"        for c in c_set:\\n\",\n    \"            if a.split('_')[0] == c.split('_')[0]:\\n\",\n    \"                relations = relation(store['ans'][a], store['ans'][c], store['pre'][a], store['pre'][c])\\n\",\n    \"                # print(relations)\\n\",\n    \"                for i in range(4):\\n\",\n    \"                    ac_metrics[i] += len(relations[i])\\n\",\n    \"    metrics_dict['ac'] = calculate_metrics(ac_metrics[0], ac_metrics[1], ac_metrics[2], ac_metrics[3])\\n\",\n    \"    abc_d_metrics = [0,0,0,0]\\n\",\n    \"    for a in a_set:\\n\",\n    \"        for b in b_set:\\n\",\n    \"            for c in c_set:\\n\",\n    \"                for d in d_set:\\n\",\n    \"                    if a.split('_')[0] == c.split('_')[0]:\\n\",\n    \"                        relations = relation_2(store['ans'][a], store['ans'][b], store['ans'][c], store['ans'][d], store['pre'][a], store['pre'][b], store['pre'][c], store['pre'][d])\\n\",\n    \"                # print(relations)\\n\",\n    \"                for i in range(4):\\n\",\n    \"                    abc_d_metrics[i] += len(relations[i])\\n\",\n    \"    metrics_dict['abc_d'] = calculate_metrics(abc_d_metrics[0], abc_d_metrics[1], abc_d_metrics[2], abc_d_metrics[3])\\n\",\n    \"\\n\",\n    \"    return metrics_dict\"\n   ]\n  },\n  {\n   \"cell_type\": \"markdown\",\n   \"id\": \"6f155d09\",\n   \"metadata\": {},\n   \"source\": [\n    \"# load output \"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 45,\n   \"id\": \"247096af\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"p = []\\n\",\n    \"a = []\\n\",\n    \"p_text = []\\n\",\n    \"a_text = []\\n\",\n    \"len_schema = stage_1_schema.copy()\\n\",\n    \"len_schema.sort(key = lambda y:len(y),reverse=True)  \\n\",\n    \"# print(len_schema)\\n\",\n    \"with open('../sii40_output.txt', 'r', encoding='utf-8') as f:\\n\",\n    \"    data = f.readlines()\\n\",\n    \"    for i ,d in enumerate(data):\\n\",\n    \"        if d.startswith('prediction'):\\n\",\n    \"            p.append(i)\\n\",\n    \"        if d.startswith('answer'):\\n\",\n    \"            a.append(i)\\n\",\n    \"    for i, ip in enumerate(p):\\n\",\n    \"        tmp = ''\\n\",\n    \"        for d in data[ip:a[i]+1]:\\n\",\n    \"            tmp+=d\\n\",\n    \"        tmp = tmp.replace('Fig. 1. ', '')\\n\",\n    \"        tmp = tmp.replace('<s>', '')\\n\",\n    \"        tmp = tmp.replace('</s>', '')\\n\",\n    \"        tmp_schema = {}\\n\",\n    \"        for ls in len_schema:\\n\",\n    \"            for t in tmp.split('\\\\n'):\\n\",\n    \"                if ls in t:\\n\",\n    \"                    pos = t.find(ls+': ')\\n\",\n    \"                    value = t[pos+len(ls+': '):]\\n\",\n    \"                    if ls not in tmp_schema.keys():   \\n\",\n    \"                        if value.endswith(','):\\n\",\n    \"                            value = value[:-1]\\n\",\n    \"                        if '#' in value:\\n\",\n    \"                            value = value.replace('#', '')\\n\",\n    \"                        tmp_schema[ls] = value.strip()\\n\",\n    \"        p_text.append(tmp_schema)\\n\",\n    \"        # print(tmp_schema)\\n\",\n    \"        # print('\\\\n')\\n\",\n    \"    for i, ia in enumerate(a):\\n\",\n    \"        tmp = ''\\n\",\n    \"        if i!=39:\\n\",\n    \"            end = p[i+1]\\n\",\n    \"        else:\\n\",\n    \"            end = len(data)\\n\",\n    \"        for d in data[ia:end]:\\n\",\n    \"            tmp+=d\\n\",\n    \"        \\n\",\n    \"        tmp = tmp.replace('answer --> ', '')\\n\",\n    \"        tmp = tmp.replace('<s>', '')\\n\",\n    \"        tmp = tmp.replace('</s>', '')\\n\",\n    \"        tmp_schema = {}\\n\",\n    \"        for idx, t in enumerate(tmp.split('\\\\n')[:-1]):\\n\",\n    \"            sche = stage_1_schema[idx]\\n\",\n    \"            if sche in t:\\n\",\n    \"                value = t.replace(sche+': ', '')\\n\",\n    \"                if sche == 'Module':\\n\",\n    \"                    tmp_schema[sche] = value.strip()\\n\",\n    \"                else:\\n\",\n    \"                    tmp_schema[sche] = value[:-1].strip()\\n\",\n    \"        a_text.append(tmp_schema)\\n\",\n    \"        # print(tmp_schema)\\n\",\n    \"        # print('\\\\n')\"\n   ]\n  },\n  {\n   \"cell_type\": \"markdown\",\n   \"id\": \"6ae636a1\",\n   \"metadata\": {},\n   \"source\": [\n    \"# IE + RE\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 46,\n   \"id\": \"d132cafc\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"ie_total (0.8834, 0.8611, 0.8714, 0.8611)\\n\",\n      \"ab_relation (0.7886, 0.7531, 0.7681, 0.7531)\\n\",\n      \"ac_relation (0.7263, 0.6722, 0.6942, 0.6722)\\n\",\n      \"abc_d_relation (0.7197, 0.6584, 0.6823, 0.6584)\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"# round(precision,4), round(recall,4), round(f1,4), round(acc,4)\\n\",\n    \"def total(metric):\\n\",\n    \"    p = 0\\n\",\n    \"    r = 0\\n\",\n    \"    f = 0\\n\",\n    \"    a = 0\\n\",\n    \"    for i in metric:\\n\",\n    \"        p += i[0]\\n\",\n    \"        r += i[1]\\n\",\n    \"        f += i[2]\\n\",\n    \"        a += i[3]\\n\",\n    \"    precision = p/len(metric)\\n\",\n    \"    recall = r/len(metric)\\n\",\n    \"    f1 = f/len(metric)\\n\",\n    \"    acc = a/len(metric)\\n\",\n    \"    return round(precision,4), round(recall,4), round(f1,4), round(acc,4)\\n\",\n    \"\\n\",\n    \"ie = []\\n\",\n    \"ab = []\\n\",\n    \"ac = []\\n\",\n    \"abc_d = []\\n\",\n    \"for i, p in enumerate(p_text):\\n\",\n    \"    # print(p)\\n\",\n    \"    # print(a_text[i])\\n\",\n    \"    m = metrics(a_text[i], p)\\n\",\n    \"    if m:\\n\",\n    \"        ie.append(m['ie'])\\n\",\n    \"        ab.append(m['ab'])\\n\",\n    \"        ac.append(m['ac'])\\n\",\n    \"        abc_d.append(m['abc_d'])\\n\",\n    \"print('ie_total', total(ie))\\n\",\n    \"print('ab_relation', total(ab))\\n\",\n    \"print('ac_relation', total(ac))\\n\",\n    \"print('abc_d_relation', total(abc_d))\\n\"\n   ]\n  },\n  {\n   \"cell_type\": \"markdown\",\n   \"id\": \"251270b5\",\n   \"metadata\": {},\n   \"source\": [\n    \"# each set IE score\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 47,\n   \"id\": \"5f51c1bd\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def metrics_single(answers, predictions, set_name):\\n\",\n    \"    keys = ['tp', 'fp', 'fn', 'ans', 'pre']\\n\",\n    \"    store = {'tp':{'total':0},'fp':{'total':0},'fn':{'total':0},'ans':{'total':0}, 'pre':{'total':0}}\\n\",\n    \"    metrics_dict = {}\\n\",\n    \"    for i, answer in enumerate(list(answers.items())): \\n\",\n    \"        if answer[0] in set_name:\\n\",\n    \"            if answer[0] in predictions.keys():\\n\",\n    \"                acc_prediction = (answer[0], predictions[answer[0]])\\n\",\n    \"            else:\\n\",\n    \"                return None\\n\",\n    \"            metrics = single_match(answer, acc_prediction)\\n\",\n    \"            for idx in range(4):\\n\",\n    \"                store[keys[idx]]['total'] +=len(metrics[idx])\\n\",\n    \"            for idx in range(5):\\n\",\n    \"                store[keys[idx]][answer[0]]=metrics[idx]     \\n\",\n    \"    metrics_dict['ie'] = calculate_metrics(store['tp']['total'], store['fp']['total'], store['fn']['total'], store['ans']['total'])\\n\",\n    \"    return metrics_dict\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 48,\n   \"id\": \"432300d7\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"a_ie (0.8354, 0.8123, 0.821, 0.8123)\\n\",\n      \"b_ie (0.902, 0.902, 0.902, 0.902)\\n\",\n      \"c_ie (0.828, 0.7831, 0.8014, 0.7831)\\n\",\n      \"d_ie (0.9796, 0.9796, 0.9796, 0.9796)\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"# round(precision,4), round(recall,4), round(f1,4), round(acc,4)\\n\",\n    \"a = []\\n\",\n    \"b = []\\n\",\n    \"c = []\\n\",\n    \"d = []\\n\",\n    \"for i, p in enumerate(p_text):\\n\",\n    \"    m = metrics_single(a_text[i], p, a_set)\\n\",\n    \"    if m:\\n\",\n    \"        a.append(m['ie'])\\n\",\n    \"for i, p in enumerate(p_text):\\n\",\n    \"    m = metrics_single(a_text[i], p, b_set)\\n\",\n    \"    if m:\\n\",\n    \"        b.append(m['ie'])\\n\",\n    \"for i, p in enumerate(p_text):\\n\",\n    \"    m = metrics_single(a_text[i], p, c_set)\\n\",\n    \"    if m:\\n\",\n    \"        c.append(m['ie'])\\n\",\n    \"for i, p in enumerate(p_text):\\n\",\n    \"    m = metrics_single(a_text[i], p, d_set)\\n\",\n    \"    if m:\\n\",\n    \"        d.append(m['ie'])\\n\",\n    \"\\n\",\n    \"print('a_ie', total(a))\\n\",\n    \"print('b_ie', total(b))\\n\",\n    \"print('c_ie', total(c))\\n\",\n    \"print('d_ie', total(d))\"\n   ]\n  },\n  {\n   \"cell_type\": \"markdown\",\n   \"id\": \"f43b76a4\",\n   \"metadata\": {},\n   \"source\": [\n    \"# deduction, normalization, summarization\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 49,\n   \"id\": \"3afa7a07\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"deduction = ['Cell_area_measured', 'Cell_architecture', 'Cell_semitransparent']\\n\",\n    \"normalization = ['Perovskite_deposition_thermal_annealing_time', 'Stability_time_total_exposure', 'Cell_area_measured']\\n\",\n    \"summarization=['Substrate_stack_sequence', 'ETL_stack_sequence', 'Perovskite_composition_short_form', 'HTL_stack_sequence']\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 64,\n   \"id\": \"825717d6\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"with open('original_text.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    prompts = json.load(f)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 65,\n   \"id\": \"8e8740f0\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"40\\n\",\n      \"{'Perovskite_deposition_thermal_annealing_temperature': '90', 'Perovskite_deposition_thermal_annealing_time': '40', 'Stability_average_over_n_number_of_cells': '1', 'Cell_semitransparent_wavelength_range': 'nan; nan', 'Cell_number_of_cells_per_substrate': '0', 'Perovskite_composition_short_form': 'MAPbI', 'Perovskite_composition_long_form': 'MAPbI3', 'Backcontact_deposition_procedure': 'Evaporation', 'Perovskite_deposition_procedure': 'Spin-coating', 'Backcontact_additives_compounds': '', 'Stability_PCE_end_of_experiment': '', 'Perovskite_additives_compounds': '', 'Perovskite_deposition_solvents': 'Unknown', 'Stability_time_total_exposure': '', 'Stability_temperature_range': 'nan; nan', 'Stability_PCE_initial_value': '', 'Backcontact_stack_sequence': 'Ag', 'Substrate_stack_sequence': 'SLG | ITO', 'ETL_deposition_procedure': 'Spin-coating', 'HTL_deposition_procedure': 'Spin-coating', 'ETL_additives_compounds': 'BCP', 'HTL_additives_compounds': '', 'Stability_atmosphere': 'Unknown', 'Cell_semitransparent': 'FALSE', 'ETL_stack_sequence': 'PCBM-60', 'HTL_stack_sequence': 'PEDOT:PSS', 'Stability_measured': 'FALSE', 'Cell_area_measured': '0.1', 'Cell_architecture': 'pin', 'Cell_flexible': 'FALSE', 'Module': 'FALSE'}\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"p = []\\n\",\n    \"a = []\\n\",\n    \"p_text = []\\n\",\n    \"a_text = []\\n\",\n    \"len_schema = stage_1_schema.copy()\\n\",\n    \"len_schema.sort(key = lambda y:len(y),reverse=True)  \\n\",\n    \"# print(len_schema)\\n\",\n    \"with open('../sii40_output.txt', 'r', encoding='utf-8') as f:\\n\",\n    \"    data = f.readlines()\\n\",\n    \"    for i ,d in enumerate(data):\\n\",\n    \"        if d.startswith('prediction'):\\n\",\n    \"            p.append(i)\\n\",\n    \"        if d.startswith('answer'):\\n\",\n    \"            a.append(i)\\n\",\n    \"    for i, ip in enumerate(p):\\n\",\n    \"        tmp = ''\\n\",\n    \"        for d in data[ip:a[i]+1]:\\n\",\n    \"            tmp+=d\\n\",\n    \"        tmp = tmp.replace('Fig. 1. ', '')\\n\",\n    \"        tmp = tmp.replace('<s>', '')\\n\",\n    \"        tmp = tmp.replace('</s>', '')\\n\",\n    \"        tmp_schema = {}\\n\",\n    \"        for ls in len_schema:\\n\",\n    \"            for t in tmp.split('\\\\n'):\\n\",\n    \"                if ls in t:\\n\",\n    \"                    pos = t.find(ls+': ')\\n\",\n    \"                    value = t[pos+len(ls+': '):]\\n\",\n    \"                    if ls not in tmp_schema.keys():   \\n\",\n    \"                        if value.endswith(','):\\n\",\n    \"                            value = value[:-1]\\n\",\n    \"                        if '#' in value:\\n\",\n    \"                            value = value.replace('#', '')\\n\",\n    \"                        tmp_schema[ls] = value.strip()\\n\",\n    \"        p_text.append(tmp_schema)\\n\",\n    \"        # print(tmp_schema)\\n\",\n    \"        # print('\\\\n')\\n\",\n    \"    for i, ia in enumerate(a):\\n\",\n    \"        tmp = ''\\n\",\n    \"        if i!=39:\\n\",\n    \"            end = p[i+1]\\n\",\n    \"        else:\\n\",\n    \"            end = len(data)\\n\",\n    \"        for d in data[ia:end]:\\n\",\n    \"            tmp+=d\\n\",\n    \"        \\n\",\n    \"        tmp = tmp.replace('answer --> ', '')\\n\",\n    \"        tmp = tmp.replace('<s>', '')\\n\",\n    \"        tmp = tmp.replace('</s>', '')\\n\",\n    \"        tmp_schema = {}\\n\",\n    \"        for idx, t in enumerate(tmp.split('\\\\n')[:-1]):\\n\",\n    \"            sche = stage_1_schema[idx]\\n\",\n    \"            if sche in t:\\n\",\n    \"                value = t.replace(sche+': ', '')\\n\",\n    \"                if sche == 'Module':\\n\",\n    \"                    tmp_schema[sche] = value.strip()\\n\",\n    \"                else:\\n\",\n    \"                    tmp_schema[sche] = value[:-1].strip()\\n\",\n    \"        a_text.append(tmp_schema)\\n\",\n    \"        # print(tmp_schema)\\n\",\n    \"        # print('\\\\n')\\n\",\n    \"print(len(p_text))\\n\",\n    \"print(p_text[0])\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 66,\n   \"id\": \"f2af9bfc\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"d_f_t = 0\\n\",\n    \"d_f = 0\\n\",\n    \"d_n_t = 0\\n\",\n    \"d_n = 0\\n\",\n    \"d_s_t = 0\\n\",\n    \"d_s = 0\\n\",\n    \"for i, p in enumerate(p_text):\\n\",\n    \"    for idx, a in enumerate(a_text[i].keys()):\\n\",\n    \"        if a in deduction:\\n\",\n    \"            if a in p.keys() and a_text[i][a] not in prompts[i]:\\n\",\n    \"                d_f_t += 1\\n\",\n    \"                if p[a]==a_text[i][a]:\\n\",\n    \"                    d_f += 1\\n\",\n    \"        if a in normalization:\\n\",\n    \"            if a in p.keys() and a_text[i][a] not in prompts[i]:\\n\",\n    \"                d_n_t += 1\\n\",\n    \"                if p[a]==a_text[i][a]:\\n\",\n    \"                    d_n += 1\\n\",\n    \"                else:\\n\",\n    \"                    # print(p[a], a_text[i][a])\\n\",\n    \"                    a_words = a_text[i][a].replace('; ',' >> ').replace(' | ', ' >> ').split(' >> ')\\n\",\n    \"                    p_words = p[a].replace('; ',' >> ').replace(\\\"''\\\", '').split(' >> ')\\n\",\n    \"                    for pw in p_words:\\n\",\n    \"                        if pw in a_words:\\n\",\n    \"                            d_n += 1\\n\",\n    \"                        else:\\n\",\n    \"                            # print(a_words,p_words)\\n\",\n    \"                            for aw in a_words:\\n\",\n    \"                                if if_float(pw) and if_float(aw):\\n\",\n    \"                                    if round(float(pw),1) == round(float(aw),1):\\n\",\n    \"                                        # print('sub', pw, aw)\\n\",\n    \"                                        d_n += 1\\n\",\n    \"        if a in summarization:\\n\",\n    \"            if a in p.keys(): \\n\",\n    \"                a_words = a_text[i][a].replace('|',';').replace(':',';').replace('>>',';').replace('Spin-coating','spin-coated').split(';')\\n\",\n    \"                a_words = [x.strip() for x in a_words]\\n\",\n    \"                p_words = p[a].replace('|',';').replace(':',';').replace('>>',';').replace('Spin-coating','spin-coated').split(';')\\n\",\n    \"                p_words = [x.strip() for x in p_words] \\n\",\n    \"                for aw in a_words:\\n\",\n    \"                    if aw not in prompts[i]:\\n\",\n    \"                        d_s_t += 1\\n\",\n    \"                        if aw in p_words:\\n\",\n    \"                            d_s += 1\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 67,\n   \"id\": \"bcc6a788\",\n   \"metadata\": {\n    \"pycharm\": {\n     \"name\": \"#%%\\n\"\n    }\n   },\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"53 70 0.7571428571428571\\n\",\n      \"29 41 0.7073170731707317\\n\",\n      \"116 154 0.7532467532467533\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"print(d_f, d_f_t, d_f/d_f_t)\\n\",\n    \"print(d_n, d_n_t, d_n/d_n_t)\\n\",\n    \"print(d_s, d_s_t, d_s/d_s_t)\\n\",\n    \"\\n\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"b5aacba9\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"'''\\n\",\n    \"# GPT-3 finetune result\\n\",\n    \"fine_data = []\\n\",\n    \"with open('test_output40.txt', 'r', encoding='utf-8') as f:\\n\",\n    \"    data = f.readlines()\\n\",\n    \"    for d in data:\\n\",\n    \"        if d.startswith('output'):\\n\",\n    \"            fine_data.append(d[:-1].replace('output:  ', ''))\\n\",\n    \"p_text = []\\n\",\n    \"for fd in fine_data:\\n\",\n    \"    pos = []\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    for i in stage_1_schema:\\n\",\n    \"        pos.append(fd.find(i))\\n\",\n    \"    for i, e in enumerate(stage_1_schema):\\n\",\n    \"        if i!=len(pos)-1:\\n\",\n    \"            end = pos[i+1]-2\\n\",\n    \"        else:\\n\",\n    \"            end = -1\\n\",\n    \"        if end == -1:\\n\",\n    \"            content = fd[pos[i]+2+len(e):]\\n\",\n    \"        else:\\n\",\n    \"            content = fd[pos[i]+2+len(e):end]\\n\",\n    \"        tmp_dict[e] = content.replace(\\\"''\\\", '')\\n\",\n    \"    p_text.append(tmp_dict)\\n\",\n    \"# print(len(p_text))\\n\",\n    \"# print(p_text[0])\\n\",\n    \"'''\"\n   ]\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.8.8\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "SII_MDP/sii_test.py",
    "content": "import torch\r\nfrom transformers import LlamaTokenizer, LlamaForCausalLM, GenerationConfig\r\nimport json\r\nimport sys\r\n\r\n\r\nmodel_path = str(sys.argv[1])\r\ndata_path = str(sys.argv[2])\r\n\r\n\r\ndef generate_prompt(prompt_instruction, prompt_input):\r\n    return \"instruction: \" + str(prompt_instruction) + \"If prediction is finished, add </s> at the end of the output., input: \" + str(prompt_input)\r\n\r\n \r\ndef generate_prediction(model_path,data_path):\r\n    #load the model\r\n    tokenizer = LlamaTokenizer.from_pretrained(model_path)\r\n    model = LlamaForCausalLM.from_pretrained(\r\n        model_path,\r\n        load_in_8bit=False,\r\n        torch_dtype=torch.float16,\r\n        device_map=\"auto\"\r\n    )\r\n    with open(data_path,'r') as f:\r\n        data = json.load(f)\r\n\r\n    instructions = []\r\n    true_output = []\r\n    pred_output = []\r\n    c = 0\r\n    print(len(data))\r\n    for i in data:\r\n        print(\"-----------------------------\")\r\n        print(c)\r\n        c+=1\r\n        text = generate_prompt(i['instruction'], i['input'])\r\n        input_ids= tokenizer(text, return_tensors=\"pt\").input_ids.to(\"cuda\") \r\n        generated_ids = model.generate(\r\n            input_ids, \r\n            max_length=2048,\r\n            do_sample=True, \r\n            repetition_penalty=1.0, \r\n            temperature=0.8, \r\n            top_p=0.75, \r\n            top_k=40\r\n        )\r\n        output = tokenizer.decode(generated_ids[0])\r\n        print(output)\r\n        output_text = \"\"\r\n        if output.split(\"add </s> at the end of the output.\")[1].count(\"</s>\") >= 1:\r\n            output_text = output\r\n        while output.split(\"add </s> at the end of the output.\")[1].count(\"</s>\") < 1:\r\n            input_ids= tokenizer(\"Continue. If prediction is finished, add </s> at the end of the output.\", return_tensors=\"pt\").input_ids.to(\"cuda\") \r\n            generated_ids = model.generate(\r\n                input_ids, \r\n                max_length=2048,\r\n                do_sample=True, \r\n                repetition_penalty=1.0, \r\n                temperature=0.8, \r\n                top_p=0.75, \r\n                top_k=40\r\n            )\r\n            output = tokenizer.decode(generated_ids[0])\r\n            output_text = output_text + \"\\n\" + \"continue ->\\n\" + output\r\n            print(\"continue -> \" + output)\r\n\r\n\r\n        true_value = i['output']\r\n        instructions.append(i['instruction'])\r\n        true_output.append(true_value)\r\n        pred_output.append(output_text)\r\n    return true_output,pred_output\r\n\r\n\r\ntrue_output,pred_output = generate_prediction(model_path,data_path)\r\noutput_name = data_path.replace('.json','')\r\nf = open(output_name+'_output.txt','w')\r\nfor line in range(len(pred_output)):\r\n    f.write(\"prediction --> \"+pred_output[line]+'\\n')\r\n    f.write(\"answer --> \"+true_output[line]+'\\n')\r\nf.close()\r\n"
  },
  {
    "path": "dataset/Crystalline organic-inorganic compounds/DukeDB.csv",
    "content": "doi,compound name,formula,group,organic,inorganic,iupac,dimensionality,sample type,code,level of theory,Exchange-correlation functional,k-point grid,level of relativity,basis set definition,numerical accuracy,synthesis starting materials,synthesis product,synthesis description,experimental method,experimental description\r\n10.1002/adfm.201903528,Methylammonium germanium bromide,CH6NGeBr3,\"Methanaminium tribromogermanate(II), MAGeBr3, CH3NH3GeBr3\",CH6N,\"GeBr3, Germanium bromide\",methanaminium germanium bromide,3,powder,,,,,,,,\"HBr, H3PO2, GeO2, CH3NH3Br\",CH3NH3GeBr3,\"All operations were carried out under high purity nitrogen. A two-neck flask was charged with a mixture of 48% w/w aqueous HBr (3.0 mL, 55.2 mmol) and 50% w/w aqueous H3PO2(2.0 mL, 18.2 mmol). GeO2 powder (209 mg, 2 mmol) was dissolved in the mixture by heating the flask to 140 °C in an oil bath, under constant magnetic stirring for about 20 min, which formed a bright pale-yellow solution. Subsequently, a stoichiometric amount of solid CH3NH3Br (224 mg, 2 mmol) was added to the hot solution and dissolved then. 20 min later, the stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, lemon yellow, granular crystals were precipitated. After being kept in the solution overnight, the crystals were collected by suction filtration and dried under reduced pressure\",,\r\n10.1002/adfm.201903528,Butylammonium germanium bromide,C4H12NGeBr4,\"Butan-1-aminium tetrabromogermanate(II), BA2GeBr4\",C4H12N,\"GeBr4, Germanium bromide\",butan-1-aminium germanium bromide,2,single crystal,,,,,,,,\"HBr, H3PO2, GeO2, n−  CH3(CH2)3NH2, n−  CH3(CH2)3NH3Br\",C4H12NGeBr4,\"A two-neck flask was charged with a mixture of 48% w/w aqueous HBr (2.0 mL, 36.8 mmol) and 50% w/w aqueous H3PO2 (3.0 mL, 27.3 mmol). GeO2 powder (209 mg, 2 mmol) was dissolved in the mixture by heating the flask to 140 °C in an oil bath, under constant magnetic stirring for about 20 min, which formed a bright pale-yellow solution. In a separate flask, n− CH3(CH2)3NH2(197 μL, 2 mmol) was neutralized with 48% w/w aqueous HBr (2 mL, 36.8 mmol) in an ice bath, resulting a transparent solution. The n− CH3(CH2)3NH3Br solution was then added dropwise into the two-neck flask. After being gradually heated to about 160 °C in 30 min, the stirring was discontinued, and the solution was left to cool down to freezing temperature, resulting in the precipitation of white lamellar crystals. After being kept in the solution overnight, the crystals were collected by suction filtration and dried under reduced pressure.\",,\r\n10.1002/adma.201505002,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,single crystal,,,,,,,,\"Lead (II) acetate trihydrate (Pb(ac) 2·3H2O, 99%), fomamidine acetate salt (FAac, 99%), lead iodide (PbI2 , 99.999%), hydriodic acid (HI) (57% w/w aq. soln., stabilized with H3PO2), and gamma-butyrolactone (GBL, 99%) were purchased from Sigma-Aldrich\",FAPbI3 Single-crystal 5 mm yellow,\"Synthesis of Seed Crystal of FAPbI3: \r\nDissolve 2.5 g Pb(ac)2 ·3H2O in 15 mL of HI in a 100 mL flask in a 105 °C oil bath. Add 1.5 mL HI solution and 0.7 g of FAac to the mixed acid solution. Decrease the temperature of the mixed solution to 70 °C; maintain temperature for 6 h for the precipitation of seed crystal FAPbI3 (≈1 mm in size). Wash crystals with diethyl ether and dry in vacuum. \r\n\r\nSynthesis of Single Crystal FAPbI3: \r\nDissolve 1.0 M solution containing PbI2 and FAI (1:1) was in GBL at 60 °C overnight. Filter the solution using PTFE filter with 0.2 µm pore size. Place seed crystals into this GBL solution in oil bath ≈100–105 °C for 3 h to grow larger crystals. Replace with fresh precursor to obtain an even larger crystal. Repeat this process three times to obtain a large single crystal FAPbI3 in alpha phase. The crystals turn to the yellow delta-phase in 10 days.\r\n\r\nRefer to Page 2257 Experimental section.\",Photoluminescence,NKT SuperK Extreme laser with an excitation of 475 nm and New Focus Si fW detector. Refer to SI Figure S5.\r\n10.1002/adma.201505002,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,single crystal,,,,,,,,\"Lead (II) acetate trihydrate (Pb(ac) 2·3H2O, 99%), fomamidine acetate salt (FAac, 99%), lead iodide (PbI2 , 99.999%), hydriodic acid (HI) (57% w/w aq. soln., stabilized with H3PO2), and gamma-butyrolactone (GBL, 99%) were purchased from Sigma-Aldrich\",FAPbI3 Single-crystal 5 mm black,Synthesis of Seed Crystal of FAPbI3: Dissolve 2.5 g Pb(ac)2 ·3H2O in 15 mL of HI in a 100 mL flask in a 105 °C oil bath. Add 1.5 mL HI solution and 0.7 g of FAac to the mixed acid solution. Decrease the temperature of the mixed solution to 70 °C; maintain temperature for 6 h for the precipitation of seed crystal FAPbI3 (≈1 mm in size). Wash crystals with diethyl ether and dry in vacuum. Synthesis of Single Crystal FAPbI3: Dissolve 1.0 M solution containing PbI2 and FAI (1:1) was in GBL at 60 °C overnight. Filter the solution using PTFE filter with 0.2 µm pore size. Place seed crystals into this GBL solution in oil bath ≈100–105 °C for 3 h to grow larger crystals. Replace with fresh precursor to obtain an even larger crystal. Repeat this process three times to obtain a large single crystal FAPbI3 in alpha phase.,Photoluminescence,\"Horiba Jobin Yvon system. Refer to Page 2255 paragraph 1, Figure 2.\"\r\n10.1002/adma.201505002,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,film,,,,,,,,\"Lead iodide (PbI2 , 99.999%) were purchased from Sigma-Aldrich, formamidinium iodide (FAI) was purchased from Dyesol Limited (Australia), dimethylformamide, ITO\",FAPbI3 Thin film on ITO,Dissolve 450 mg of PbI2 in 1 mL dimethylformamide and spincoat on indium-tin-oxide (ITO) substrates at 2500 rpm for 30 s. Spincoat FAI (dissolved in 2-propanol) on top of dried PbI2 at room temperature at 3000 rpm for 30 s in dry air. Anneal films in air at 150 °C for desired time.,Photoluminescence,[ASSUMED] Horiba Jobin Yvon system. Refer to SI Figure S3.\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead bromide,(C6H14N)2PbBr4,\"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",C6H14N,\"PbBr4, Lead bromide\",bis(cyclohexylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"Cyclohexylammonium bromide, PbBr2, HBr\",\"large, pale-yellow crystals\",\"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",Single crystal X-ray diffraction,\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead bromide,(C6H14N)2PbBr4,\"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",C6H14N,\"PbBr4, Lead bromide\",bis(cyclohexylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"Cyclohexylammonium bromide, PbBr2, HBr\",\"large, pale-yellow crystals\",\"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",Single crystal X-ray diffraction,\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead bromide,(C6H14N)2PbBr4,\"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",C6H14N,\"PbBr4, Lead bromide\",bis(cyclohexylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"Cyclohexylammonium bromide, PbBr2, HBr\",\"large, pale-yellow crystals\",\"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",Physical Properties Measurement,\"Measured with precision impedance analyzer (Model: Agilent 4294A, Santa Clara, CA). Measured at 1 MHz.\"\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead bromide,(C6H14N)2PbBr4,\"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",C6H14N,\"PbBr4, Lead bromide\",bis(cyclohexylaminium) lead (II) bromide,2,bulk polycrystalline,,,,,,,,\"Cyclohexylammonium bromide, PbBr2, HBr\",\"large, pale-yellow crystals\",\"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",UV-vis absorption (diffuse reflectance),\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead bromide,(C6H14N)2PbBr4,\"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",C6H14N,\"PbBr4, Lead bromide\",bis(cyclohexylaminium) lead (II) bromide,2,unknown,CASTEP Program,DFT,GGA-PBE,3x3x3,,Norm-conserving pseudopotential,,\"Cyclohexylammonium bromide, PbBr2, HBr\",\"large, pale-yellow crystals\",\"First, CHA was synthesized by mixing Cyclohexylammonium bromide (20 mmol, 3.60 g), PbBr2 (10 mmol, 3.67 g) and HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Finally, large, pale yellow crystals of (CHA)2PbBr3 were obtained by cooling the solution at a rate of 0.125 K/h\",,\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead bromide,(C6H14N)2PbBr4,\"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",C6H14N,\"PbBr4, Lead bromide\",bis(cyclohexylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"Cyclohexylammonium bromide, PbBr2, HBr\",\"large, pale-yellow crystals\",\"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",UV-vis absorption (diffuse reflectance),\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead iodide,(C6H14N)2PbI4,\"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",C6H14N,\"PbI4, Lead iodide\",bis(cyclohexylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"cyclohexylamine, PbI2, HI\",\"Large, orange crystals\",\"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",Single crystal X-ray diffraction,\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead iodide,(C6H14N)2PbI4,\"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",C6H14N,\"PbI4, Lead iodide\",bis(cyclohexylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"cyclohexylamine, PbI2, HI\",\"Large, orange crystals\",\"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",Single crystal X-ray diffraction,\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead iodide,(C6H14N)2PbI4,\"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",C6H14N,\"PbI4, Lead iodide\",bis(cyclohexylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"cyclohexylamine, PbI2, HI\",\"Large, orange crystals\",\"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",UV-vis absorption (diffuse reflectance),\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead iodide,(C6H14N)2PbI4,\"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",C6H14N,\"PbI4, Lead iodide\",bis(cyclohexylaminium) lead (II) iodide,2,unknown,CASTEP Program,DFT,GGA-PBE,3x3x3,,Norm-conserving pseudopotential,energy cutoff: 820 eV,\"cyclohexylamine, PbI2, HI\",\"Large, orange crystals\",\"First, cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals soon grew by cooling the solution at a rate of 0.125 K/h.\",,\r\n10.1002/adma.201505224,Bis(cyclohexylammonium) lead iodide,(C6H14N)2PbI4,\"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",C6H14N,\"PbI4, Lead iodide\",bis(cyclohexylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"cyclohexylamine, PbI2, HI\",\"Large, orange crystals\",\"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",UV-vis absorption (diffuse reflectance),\r\n10.1002/adma.201606405,Formamidinium lead bromide,CH5N2PbBr3,\"Methanimidamide tribromoplumbate(II), FAPBr3, FAPBr, (FA)PbBr3 HC(NH2)2PbBr3, (NH2)2CHPbBr3\",CH5N2,\"PbBr3, Lead bromide\",Imidoformamidinium lead(II) bromide,3,film,,,,,,,,\"FABr, PbBr2, CsBr, toluene, THF\",Thin film/Solution,\"Add mixture of precursors drop-wise into the toluene solution for NC formation, and centrifuge the final product. Disperse NCs in THF with a concentration of 20 mg mL−1. Refer to Page 2 paragraph 4; Figure 2(a).\",UV-Vis absorption,Instrumental details not provided. Refer to Page 3 paragraph 2; Figure 2(d); SI Table S2.\r\n10.1002/adma.201606405,Formamidinium(1-x) cesium(x) lead bromide: x = 0.6,FA(0.4)Cs(0.6)PbBr3,\"Methanimidamide cesium tribromoplumbate(II), FA0.4Cs0.6PBr3, FAPBr, (FA)CsPbBr3 HC(NH2)2CsPbBr3, (NH2)2CHPbBr3\",CH5N2,\"Cs0.6PbBr3, Lead bromide\",Imidoformamidinium cesium lead(II) bromide,3,film,,,,,,,,\"FABr, PbBr2, CsBr, toluene, THF\",Thin film,\"Add mixture of precursors drop-wise into the toluene solution for NC formation, and centrifuge the final product. Disperse NCs in THF with a concentration of 20 mg mL−1. Refer to Page 2 paragraph 4; Figure 2(a).\",Photoluminescence,Instrumental details not provided. Refer to Page 3 paragraph 2; Figure 2(e); SI Table S2.\r\n10.1002/adma.201906571,Bis(phenethylammonium) tris(formamidinium) lead bromide,(PEA)2(FA)3Pb4Br13,\"(PEA)2(FA)3Pb4Br13, bis(phenethylaminium) tris(diaminomethanide) tridecabromo tetraplumbate(II)\",\"C8H12N, CH5N2\",\"Pb4Br13, Lead bromide\",bis(phenethylaminium) tris(diaminomethanide) lead bromide,3,film,,,,,,,,,,,UV-VIS Spectroscopy,Films of quasi-2D perovskite (PEA)2(FA)3Pb4Br13 were prepared from the DMSO and NMP solvents to measure their absorbance vs wavelength intensity.\r\n10.1002/adma.201906571,Bis(phenethylammonium) tris(formamidinium) lead bromide,(PEA)2(FA)3Pb4Br13,\"(PEA)2(FA)3Pb4Br13, bis(phenethylaminium) tris(diaminomethanide) tridecabromo tetraplumbate(II)\",\"C8H12N, CH5N2\",\"Pb4Br13, Lead bromide\",bis(phenethylaminium) tris(diaminomethanide) lead bromide,3,film,,,,,,,,,,,Photoluminescence,Optical properties of quasi-2D perovskite (PEA)2(FA)3Pb4Br13 films prepared from solvent DMSO and NMP and were then measured via Photoluminescence to obtain their PL intensity at certain wavelengths.\r\n10.1002/adma.202005868,bis[S-(−)-1-(1-naphthyl)ethylammonium] lead bromide,S-[C10H7CH(CH3)NH3]2PbBr4,\"S-NPB, bis[S-(−)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",C12NH14,\"PbBr4, Lead bromide\",bis(S-(−)-1-(1-naphthyl)ethylammonium) lead (II) bromide,2,single crystal,,,,,,,,\"(S)-(−)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",[S-(−)-1-(1-naphthyl)ethylammonium]2PbBr4,\"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(−)-1-\r\n(1-naphthyl)ethylamine (78 µL, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 °C. The hot solution was slowly cooled to room temperature (21  °C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",Differential Scanning Calorimetry,\"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 °C; enthalpy of melting: 28.71 J g−1), which upon repeating the experiment showed an acceptable temperature offset of 0.2  °C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 °C min−1. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (≈5.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  °C at a ramp rate of 5  °C min−1. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (≈5.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5°C min−1 over a temperature range from 25 to 185 °C and heated isothermally at 185 °C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  °C min−1. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g−1)/ramp rate (°C s−1) and temperature.\r\n\r\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 °C min−1 ramping rate from 25 to 300 °C under nitrogen gas flow (40 mL min−1) with samples (≈4.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\"\r\n10.1002/adma.202005868,bis[S-(−)-1-(1-naphthyl)ethylammonium] lead bromide,S-[C10H7CH(CH3)NH3]2PbBr4,\"S-NPB, bis[S-(−)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",C12NH14,\"PbBr4, Lead bromide\",bis(S-(−)-1-(1-naphthyl)ethylammonium) lead (II) bromide,2,bulk polycrystalline,,,,,,,,\"(S)-(−)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",[S-(−)-1-(1-naphthyl)ethylammonium]2PbBr4,\"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(−)-1-\r\n(1-naphthyl)ethylamine (78 µL, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 °C. The hot solution was slowly cooled to room temperature (21  °C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",Differential Scanning Calorimetry,\"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 °C; enthalpy of melting: 28.71 J g−1), which upon repeating the experiment showed an acceptable temperature offset of 0.2  °C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 °C min−1. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (≈5.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  °C at a ramp rate of 5  °C min−1. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (≈5.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5°C min−1 over a temperature range from 25 to 185 °C and heated isothermally at 185 °C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  °C min−1. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g−1)/ramp rate (°C s−1) and temperature.\r\n\r\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 °C min−1 ramping rate from 25 to 300 °C under nitrogen gas flow (40 mL min−1) with samples (≈4.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\"\r\n10.1002/adma.202005868,bis[S-(−)-1-(1-naphthyl)ethylammonium] lead bromide,S-[C10H7CH(CH3)NH3]2PbBr4,\"S-NPB, bis[S-(−)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",C12NH14,\"PbBr4, Lead bromide\",bis(S-(−)-1-(1-naphthyl)ethylammonium) lead (II) bromide,2,unknown,,,,,,,,\"(S)-(−)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",[S-(−)-1-(1-naphthyl)ethylammonium]2PbBr4,\"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(−)-1-\r\n(1-naphthyl)ethylamine (78 µL, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 °C. The hot solution was slowly cooled to room temperature (21  °C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",Differential Scanning Calorimetry,\"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 °C; enthalpy of melting: 28.71 J g−1), which upon repeating the experiment showed an acceptable temperature offset of 0.2  °C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 °C min−1. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (≈5.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  °C at a ramp rate of 5  °C min−1. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (≈5.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5°C min−1 over a temperature range from 25 to 185 °C and heated isothermally at 185 °C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  °C min−1. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g−1)/ramp rate (°C s−1) and temperature.\r\n\r\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 °C min−1 ramping rate from 25 to 300 °C under nitrogen gas flow (40 mL min−1) with samples (≈4.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\"\r\n10.1002/adma.202005868,bis[S-(−)-1-(1-naphthyl)ethylammonium] lead bromide,S-[C10H7CH(CH3)NH3]2PbBr4,\"S-NPB, bis[S-(−)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",C12NH14,\"PbBr4, Lead bromide\",bis(S-(−)-1-(1-naphthyl)ethylammonium) lead (II) bromide,2,unknown,,,,,,,,\"(S)-(−)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",[S-(−)-1-(1-naphthyl)ethylammonium]2PbBr4,\"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(−)-1-\r\n(1-naphthyl)ethylamine (78 µL, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 °C. The hot solution was slowly cooled to room temperature (21  °C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",Differential Scanning Calorimetry,\"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 °C; enthalpy of melting: 28.71 J g−1), which upon repeating the experiment showed an acceptable temperature offset of 0.2  °C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 °C min−1. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (≈5.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  °C at a ramp rate of 5  °C min−1. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (≈5.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5°C min−1 over a temperature range from 25 to 185 °C and heated isothermally at 185 °C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  °C min−1. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g−1)/ramp rate (°C s−1) and temperature.\r\n\r\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 °C min−1 ramping rate from 25 to 300 °C under nitrogen gas flow (40 mL min−1) with samples (≈4.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\"\r\n10.1002/adma.202005868,bis[S-(−)-1-(1-naphthyl)ethylammonium] lead bromide,S-[C10H7CH(CH3)NH3]2PbBr4,\"S-NPB, bis[S-(−)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",C12NH14,\"PbBr4, Lead bromide\",bis(S-(−)-1-(1-naphthyl)ethylammonium) lead (II) bromide,2,unknown,,,,,,,,\"(S)-(−)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",[S-(−)-1-(1-naphthyl)ethylammonium]2PbBr4,\"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(−)-1-\r\n(1-naphthyl)ethylamine (78 µL, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 °C. The hot solution was slowly cooled to room temperature (21  °C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",Thermogravimetric Analysis,Thermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 °C min−1 ramping rate from 25 to 300 °C under nitrogen gas flow (40 mL min−1) with samples (≈4.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates.\r\n10.1002/adma.202005868,1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",1-(1-naphthyl)ethanaminium lead (II) bromide,2,bulk polycrystalline,,,,,,,,\"1-(1-naphthyl) ethylamine (98%, Sigma Aldrich),  lead bromide (PbBr2, 99.99%, TCI chemicals) and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",1-(1-naphthyl)ethylammonium]2PbBr4,\"To grow rac-NPB perovskite crystals,\r\nstoichiometric amounts of PbBr2 (90 mg, 0.24 mmol) and 1-(1-naphthyl)\r\nethylamine (78 µL, 0.48 mmol) were dissolved in aq. HBr (1.0 mL) and\r\nmethanol (2.4 mL) in a sealed vial at 95 °C. The hot solution was slowly\r\ncooled to room temperature (21  °C) over a period of 24 h in a water\r\nbath, resulting in the formation of layered flakes of transparent rac-NPB\r\nsingle crystals.\",Differential Scanning Calorimetry,\"Differential Scanning Calorimetry: DSC measurements were performed\r\nusing a TA Discovery DSC instrument using various ramping rates and\r\ntemperature ranges (as described in the main text) using a hermetically\r\nsealed aluminum pan and lid. Prior to experiments, the DSC setup was\r\ncalibrated with metallic indium (melting temperature: 156.6 °C; enthalpy\r\nof melting: 28.71 J g−1\r\n), which upon repeating the experiment showed\r\nan acceptable temperature offset of 0.2  °C and melting enthalpy offset\r\nof 0.04%. Calibration and the above measurement were carried out at a\r\nramp rate of 5 °C min−1\r\n. DSC analyses of crystalline S-NPB and rac-NPB\r\nperovskites were carried out by hermetically sealing corresponding\r\ncrystals (≈5.0 mg) in aluminum pan/lid, and ramping temperature from\r\n25 to 250  °C at a ramp rate of 5  °C min−1.\"\r\n10.1002/adma.202005868,1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",1-(1-naphthyl)ethanaminium lead (II) bromide,2,bulk polycrystalline,,,,,,,,\"1-(1-naphthyl) ethylamine (98%, Sigma Aldrich),  lead bromide (PbBr2, 99.99%, TCI chemicals) and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",1-(1-naphthyl)ethylammonium]2PbBr4,\"To grow rac-NPB perovskite crystals,\r\nstoichiometric amounts of PbBr2 (90 mg, 0.24 mmol) and 1-(1-naphthyl)\r\nethylamine (78 µL, 0.48 mmol) were dissolved in aq. HBr (1.0 mL) and\r\nmethanol (2.4 mL) in a sealed vial at 95 °C. The hot solution was slowly\r\ncooled to room temperature (21  °C) over a period of 24 h in a water\r\nbath, resulting in the formation of layered flakes of transparent rac-NPB\r\nsingle crystals.\",Thermogravimetric Analysis,Thermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 °C min−1 ramping rate from 25 to 300 °C under nitrogen gas flow (40 mL min−1) with samples (≈4.5 mg) of single crystals of S-NPB and rac-NPB perovskite.\r\n10.1002/anie.201309786,Bis(3-butylidyne-1-ammonium) lead bromide,C8H16N2PbBr4,\"(BYA)2[PbBr4], C8H16Br4N2Pb, bis(3-butylidyne-1-aminium) tetrabromoplumbate(II)\",C4H8N,\"PbBr4, Lead bromide\",bis(3-butylidyne-1-aminium) lead (II) bromide,2,unknown,,,,,,,,,,,,\r\n10.1002/anie.201309786,\"Bis(1,2-diiodo-but-1-en-4-ammonium) lead bromide\",C8H16I4N2PbBr4,\"(BYA-I2)2[PbBr4], C8H16Br4I4N2Pb, bis(1,2-diiodo-but-1-en-4-aminium) tetrabromoplumbate(II)\",C4H8I2N,\"PbBr4, Lead bromide\",\"bis(1,2-diiodo-but-1-en-4-aminium) lead (II) bromide\",2,unknown,,,,,,,,,,,,\r\n10.1002/anie.201309786,Bis(but-3-en-1-ammonium) lead bromide,C8H20N2PbBr4,\"(BEA)2[PbBr4], C8H20Br4N2Pb, bis(but-3-en-1-aminium) tetrabromoplumbate(II)\",C4H10N,\"PbBr4, Lead bromide\",bis(but-3-en-1-aminium) lead (II) bromide,2,single crystal,,,,,,,,,,,,\r\n10.1002/anie.201309786,Bis(3-butylidyne-1-ammonium) lead bromide,C8H16N2PbBr4,\"(BYA)2[PbBr4], C8H16Br4N2Pb, bis(3-butylidyne-1-aminium) tetrabromoplumbate(II)\",C4H8N,\"PbBr4, Lead bromide\",bis(3-butylidyne-1-aminium) lead (II) bromide,2,single crystal,,,,,,,,\"(BYA)Cl (but-3-yn-1-ammonium chloride), methanol, PbBr2, 9-M HBr\",colorless crystals,\"First, 3 mL of (BYA)Cl (0.200 g, 1.89 mmol) in methanol was added to a 3-mL solution of PbBr2 (0.340 g, 0.93 mmol) in 9-M HBr at a temperature of -10ºC. The solution was stirred continuously during this process. After 15 minutes, a colorless precipitate formed and was filtered at -10º C via a glass frit and washed with cold diethyl ether.  Afterward, the colorless crystalline solid was held at reduced pressure for an hour and therefore produced 0.536 g of product. To obtain crystals appropriate for single-crystal X-ray diffraction, slow evaporation of the concentrated solution in a 1:1 methanol: HBr (9-M) was performed.\",Single-crystal X-Ray Diffraction,The data were collected using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo Kα (λ = 0.71073 Å) radiation. Data were corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\r\n10.1002/anie.201309786,\"Bis(1,2-diiodo-but-1-en-4-ammonium) lead bromide\",C8H16I4N2PbBr4,\"(BYA-I2)2[PbBr4], C8H16Br4I4N2Pb, bis(1,2-diiodo-but-1-en-4-aminium) tetrabromoplumbate(II)\",C4H8I2N,\"PbBr4, Lead bromide\",\"bis(1,2-diiodo-but-1-en-4-aminium) lead (II) bromide\",2,single crystal,,,,,,,,\"(BYA)Cl (but-3-yn-1-ammonium chloride), methanol, PbBr2, 9-M HBr, I2 crystals\",colorless crystals,\"First, 3 mL of (BYA)Cl (0.200 g, 1.89 mmol) in methanol was added to a 3-mL solution of PbBr2 (0.340 g, 0.93 mmol) in 9-M HBr at a temperature of -10ºC. The solution was stirred continuously during this process. After 15 minutes, a colorless precipitate formed and was filtered at -10º C via a glass frit and washed with cold diethyl ether. Afterward, the colorless crystalline solid was held at reduced pressure for an hour and therefore produced 0.536 g of product. 0.1 mmol of the obtained crystals were kept in a sealed darkened glass jar with 1.5 – 2.0 g of iodine crystals. The crystals were kept at reduced pressure for 30 mins to remove the surface-adsorbed iodine.\",Single-crystal X-Ray Diffraction,The data were collected using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo Kα (λ = 0.71073 Å) radiation. Data were corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\r\n10.1002/anie.201309786,Bis(but-3-en-1-ammonium) lead bromide,C8H20N2PbBr4,\"(BEA)2[PbBr4], C8H20Br4N2Pb, bis(but-3-en-1-aminium) tetrabromoplumbate(II)\",C4H10N,\"PbBr4, Lead bromide\",bis(but-3-en-1-aminium) lead (II) bromide,2,single crystal,,,,,,,,\"(BEA)Cl (but-3-en-1-ammonium chloride), methanol, PbBr2, 9-M HBr\",colorless crystals,\"First, 3 mL of (BEA)Cl (0.200 g, 1.86 mmol) in methanol was added to a 3-mL solution of PbBr2 (0.330 g, 0.90 mmol) in 9-M HBr at a temperature of -10ºC. The solution was stirred continuously during this process. After 15 minutes, a colorless precipitate formed and was filtered via a glass frit and washed with diethyl ether. This process was also executed at -10º C. Afterward, a colorless crystalline solid was held at reduced pressure for an hour and therefore produced 0.425 g of product. To obtain crystals appropriate for single-crystal X-ray diffraction, acetone was slowly diffused into a concentrated solution of the product in 9-M HBr.\",Single-crystal X-Ray Diffraction,The data were collected using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo Kα (λ = 0.71073 Å) radiation. Data were corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\r\n10.1002/anie.201406466,bis(phenylethylammonium) bis(methylammonium) lead iodide,C18H36N4Pb3I10,\"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\"C8H12N, CH6N\",\"Pb3I10, Lead iodide\",bis(2-phenylethanaminium) bismethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"lead iodide (PbI2), phenyl ethyl ammonium iodide (PEAI; synthesized from phenyl ethyl amine and HI), methylammonium iodide (MAI; synthesized from methylamine and HI), sodium iodide (NaI), acetone, nitromethane\",dark red plate-like (PEA)2(MA)2[Pb3I10] crystals,\"(PEA)I (3.60 mg, 0.0145 mmol), (MA)I (2.30 mg, 0.0145 mmol), and PbI2 (10.0 mg, 0.0217 mmol) were dissolved in a mixture of acetone (10 mL) and nitromethane (5 mL). NaI (6.50 mg, 0.0434 mmol) was added to this solution. The solvent was slowly evaporated for over 6 days to obtain the crystals.\",Single-crystal X- ray Diffraction,Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and with monochromated Mo Kα (λ = 0.71073 Å) radiation.\r\n10.1002/anie.201506449,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,single crystal,,,,,,,,\"Pb(SCN)2 (synthesized), methylammonium iodide (MAI, synthesized)\",Dark red (or black) plate-like crystals,\"0.20 g Pb(SCN)2 and 0.15 g MAI were dissolved in 0.6 mL DMF and heated under stirring to 60 degrees C. Upon cooling and evaporation of DMF, the crystals precipitated from the solution.\",Single crystal X-ray diffraction,Data was collected using Bruker APEX II with CCD and micro-source and using Mo Kα radiation (= 0.71073 Å).\r\n10.1002/anie.201806452,Cesium tin bromide (0D),Cs4SnBr6,tetracesium hexabromostannate(II),None,\"SnBr6, Tin bromide\",,0,single crystal,,,,,,,,\"Cesium bromide (CsBr, 99%, Alfa Aesar), tin (II) bromide (SnBr2, 99.2%, Alfa Aesar)\",Colorless crystals,\"Mix CsBr and SnBr2 in a 4.5:1 molar ratio, mortar, and press together into a pellet (> 5 tons of pressure, 12 mm die). Seal pellet under vacuum (10-2 – 10-3 mbar) in a Pyrex tube and heat to 350 °C for 60 hours. Open tube in the glovebox, and repeat the process until the formation of single crystals.\",Single-crystal X-ray diffraction,\"XtraLAB Synergy, Dualflex, Pilatus 300K diffractometer. PhotonJet (Cu) X-ray source (CuKα, λ=1.54184 Å; micro-focus sealed X-ray tube) and mirror monochromator. Data processed and refined with CrysAlis PRO 1.171.39.31d (Rigaku OD, 2017), SHELXS, XL, and Olex2.\"\r\n10.1002/anie.201806452,Cesium tin iodide (0D),Cs4SnI6,tetracesium hexaiodostannate(II),None,\"SnI6, Tin iodide\",,0,single crystal,,,,,,,,\"Cesium bromide (CsBr, 99%), tin (II) iodide (SnI2, 99%)\",Black crystals,\"Mix CsBr and SnI2 in a 4.5:1 molar ratio, mortar, and press together into a pellet (> 5 tons of pressure, 12 mm die). Seal pellet under vacuum (10-2 – 10-3 mbar) in a Pyrex tube and heat to 350 °C for 60 hours. Open tube in the glovebox, and repeat the process until the formation of single crystals.\",Single-crystal X-ray diffraction,\"XtraLAB Synergy, Dualflex, Pilatus 300K diffractometer. PhotonJet (Cu) X-ray source (CuKα, λ=1.54184 Å; micro-focus sealed X-ray tube) and mirror monochromator. Data processed and refined with CrysAlis PRO 1.171.39.31d (Rigaku OD, 2017), SHELXS, XL, and Olex2.\"\r\n10.1002/anie.201806452,Cesium tin iodide (0D),Cs4SnI6,tetracesium hexaiodostannate(II),None,\"SnI6, Tin iodide\",,0,single crystal,,,,,,,,\"Cesium bromide (CsBr, 99%), tin (II) iodide (SnI2, 99%)\",Black crystals,\"Mix CsBr and SnI2 in a 4.5:1 molar ratio, mortar, and press together into a pellet (> 5 tons of pressure, 12 mm die). Seal pellet under vacuum (10-2 – 10-3 mbar) in a Pyrex tube and heat to 350 °C for 60 hours. Open tube in the glovebox, and repeat the process until the formation of single crystals.\",Single-crystal X-ray diffraction,\"XtraLAB Synergy, Dualflex, Pilatus 300K diffractometer. PhotonJet (Cu) X-ray source (CuKα, λ=1.54184 Å; micro-focus sealed X-ray tube) and mirror monochromator. Data processed and refined with CrysAlis PRO 1.171.39.31d (Rigaku OD, 2017), SHELXS, XL, and Olex2.\"\r\n10.1002/anie.201807421,Cesium silver thallium chloride,Cs2AgTlCl6,Dicesium trichloroargentate(I) trichlorothalliate(III),None,Cs2AgTlCl6,,3,single crystal,,,,,,,,\"Solid CsCl, AgCl, Tl2O3, HCl, H2O\",\"dark red, truncated octahedral crystals\",\"First, solid CsCl (101 mg, 0.600 mmol), AgCl (21 mg, 0.15 mmol), and Tl2O3 (34 mg, 0.075 mmol) were mixed in a 20 mL glass with 8 mL of H2O and 8 mL of HCl (12M). This resulted in a colorless, 6M HCl solution. The vial was sealed with a polystyrene cap, heated to 100ºC for 4-6 hours until AgCl dissolved completely, and then the vial was cooled to room temperature.\",single-crystal X-ray diffraction,The frames were recorded using a Bruker D8 Venture diffractometer (with Photon 100 CMOS detector) with Mo Kα radiation (λ = 0.71073 Å). Data frames were then corrected for Lorentz/polarization using SAINT V8.38A and absorption effects using SADABS V2012.\r\n10.1002/anie.201807421,Cesium silver thallium chloride,Cs2AgTlCl6,Dicesium trichloroargentate(I) trichlorothalliate(III),None,Cs2AgTlCl6,,3,bulk polycrystalline,,,,,,,,\"Solid CsCl, AgCl, Tl2O3, HCl, H2O\",\"dark red, truncated octahedral crystals\",\"First, solid CsCl (101 mg, 0.600 mmol), AgCl (21 mg, 0.15 mmol), and Tl2O3 (34 mg, 0.075 mmol) were mixed in a 20 mL glass with 8 mL of H2O and 8 mL of HCl (12M). This resulted in a colorless, 6M HCl solution. The vial was sealed with a polystyrene cap, heated to 100ºC for 4-6 hours until AgCl dissolved completely, and then the vial was cooled to room temperature.\",UV-vis absorbance (reflectance mode),The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\r\n10.1002/anie.201807421,Cesium silver thallium chloride,Cs2AgTlCl6,Dicesium trichloroargentate(I) trichlorothalliate(III),None,Cs2AgTlCl6,,3,single crystal,VASP,DFT + one-shot GW,G0W0@HSE06,2x2x2,,PAW,,,,,,\r\n10.1002/anie.201807421,Cesium silver thallium bromide,Cs2AgTlBr6,Dicesium tribromoargentate(I) tribromothalliate(III),None,Cs2AgTlBr6,,3,single crystal,,,,,,,,\"Solid CsBr, AgBr, Tl2O3, HBr\",\"Black, truncated octahedral crystals\",\"First, solid CsBr(533 mg, 2.50 mmol), AgBr (940 mg, 5.01 mmol), and Tl2O3 (285 mg, 0.625 mmol) were mixed with 20 mL of HBr (8.9M). The vial was sealed with a polystyrene cap, heated to 100ºC for 2 hours until solids dissolved, resulting in a pale, yellow solution. Then, the vial was cooled to room temperature.\",single crystal X-ray diffraction (XRD),The frames were recorded using a Bruker D8 Venture diffractometer (with Photon 100 CMOS detector) with Mo Kα radiation (λ = 0.71073 Å). Data frames were then corrected for Lorentz/polarization using SAINT V8.38A and absorption effects using SADABS V2012.\r\n10.1002/anie.201807421,Cesium silver thallium chloride,Cs2AgTlCl6,Dicesium trichloroargentate(I) trichlorothalliate(III),None,Cs2AgTlCl6,,3,bulk polycrystalline,,,,,,,,\"Solid CsCl, AgCl, Tl2O3, HCl, H2O\",\"dark red, truncated octahedral crystals\",\"First, solid CsCl (101 mg, 0.600 mmol), AgCl (21 mg, 0.15 mmol), and Tl2O3 (34 mg, 0.075 mmol) were mixed in a 20 mL glass with 8 mL of H2O and 8 mL of HCl (12M). This resulted in a colorless, 6M HCl solution. The vial was sealed with a polystyrene cap, heated to 100ºC for 4-6 hours until AgCl dissolved completely, and then the vial was cooled to room temperature.\",UV-vis absorbance (reflectance mode),The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\r\n10.1002/anie.201807421,Cesium silver thallium bromide,Cs2AgTlBr6,Dicesium tribromoargentate(I) tribromothalliate(III),None,Cs2AgTlBr6,,3,powder,,,,,,,,\"Solid CsBr, AgBr, Tl2O3, HBr\",\"Black, truncated octahedral crystals\",\"First, solid CsBr(533 mg, 2.50 mmol), AgBr (940 mg, 5.01 mmol), and Tl2O3 (285 mg, 0.625 mmol) were mixed with 20 mL of HBr (8.9M). The vial was sealed with a polystyrene cap, heated to 100ºC for 2 hours until solids dissolved, resulting in a pale, yellow solution. Then, the vial was cooled to room temperature.\",UV-vis absorbance (reflectance mode),The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\r\n10.1002/anie.201807421,Cesium silver thallium bromide,Cs2AgTlBr6,Dicesium tribromoargentate(I) tribromothalliate(III),None,Cs2AgTlBr6,,3,bulk polycrystalline,,,,,,,,\"Solid CsBr, AgBr, Tl2O3, HBr\",\"Black, truncated octahedral crystals\",\"First, solid CsBr(533 mg, 2.50 mmol), AgBr (940 mg, 5.01 mmol), and Tl2O3 (285 mg, 0.625 mmol) were mixed with 20 mL of HBr (8.9M). The vial was sealed with a polystyrene cap, heated to 100ºC for 2 hours until solids dissolved, resulting in a pale, yellow solution. Then, the vial was cooled to room temperature.\",UV-vis absorbance (reflectance mode),The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\r\n10.1002/anie.201807421,Cesium silver thallium bromide,Cs2AgTlBr6,Dicesium tribromoargentate(I) tribromothalliate(III),None,Cs2AgTlBr6,,3,single crystal,VASP,DFT + one-shot GW,G0W0@HSE06,,,PAW,,,,,,\r\n10.1002/anie.201811497,Benzodiimidazolium tin iodide,C8H8N4SnI4,\"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",C8H8N4,\"SnI4, Tin iodide\",\"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",2,single crystal,,,,,,,,\"Benzodiimidazole, ethanol, HI, SnI2\",Black plate-like crystals,\"Benzodiimdazole was suspended in ethanol and then HI was added. The solution was refluxed for 1 hour and was then cooled to room temperature, during which solid benzodiimedazolium iodide salt precipitated. The solid were collected and were used to start the process another three times to ensure full protonation. They were then washed with ethanol and dried in vacuum to obtain an off-white solid. The perovskite was then obtained by heating stoichiometric amounts of the iodide salt with tin or lead iodide in an HI solution for 1 day before cooling.\",Single-crystal X-ray diffraction,A Bruker D8 Venture diffractometer with Mo Kalpha radiation was used. SAINT and SADABS in the APEX 3 software package was used for data reduction and absorption correction. The structure was solved using SHELXS and further refinement using SHELXL-2014 in the WINGX environment.\r\n10.1002/anie.201811497,Benzodiimidazolium tin iodide,C8H8N4SnI4,\"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",C8H8N4,\"SnI4, Tin iodide\",\"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",2,film,,,,,,,,\"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",film on glass,\"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 μl chlorobenzene was added. The film was annealed at 100 °C for 15 min.\",UV-vis absorption,Absorption measurements were performed using Perkin Elmer Lambda 950S equipped with an integrating sphere.\r\n10.1002/anie.201811497,Benzodiimidazolium tin iodide,C8H8N4SnI4,\"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",C8H8N4,\"SnI4, Tin iodide\",\"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",2,film,,,,,,,,\"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",film on glass,\"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 μl chlorobenzene was added. The film was annealed at 100 °C for 15 min.\",Photoluminescence,The spectrum was obtained using a Fluorescence Spectrometer LS 55 from PerkinElmer\r\n10.1002/anie.201811497,Benzodiimidazolium tin iodide,C8H8N4SnI4,\"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",C8H8N4,\"SnI4, Tin iodide\",\"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",2,film,,,,,,,,\"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",film on glass,\"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 μl chlorobenzene was added. The film was annealed at 100 °C for 15 min.\",Photoluminescence,The spectrum was obtained using a Fluorescence Spectrometer LS 55 from PerkinElmer\r\n10.1002/anie.201811497,Benzodiimidazolium tin iodide,C8H8N4SnI4,\"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",C8H8N4,\"SnI4, Tin iodide\",\"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",2,film,,,,,,,,\"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",film on glass,\"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 μl chlorobenzene was added. The film was annealed at 100 °C for 15 min.\",UV-vis absorption,Absorption measurements were performed using Perkin Elmer Lambda 950S equipped with an integrating sphere. The optical band gap can be estimated from the corresponding Tauc‐plot with a direct band gap assumption.\r\n10.1002/anie.201811497,Benzodiimidazolium lead iodide,C8H8N4PbI4,\"BdiPbI4, Benzodiimidazolium tetraiodoplumbate(II)\",C8H8N4,\"PbI4, Lead iodide\",\"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium lead (II) iodide\",2,single crystal,,,,,,,,\"Benzodiimidazole, ethanol, HI, PbI2\",Red plate-like crystals,\"Benzodiimdazole was suspended in ethanol and then HI was added. The solution was refluxed for 1 hour and was then cooled to room temperature, during which solid benzodiimedazolium iodide salt precipitated. The solid were collected and were used to start the process another three times to ensure full protonation. They were then washed with ethanol and dried in vacuum to obtain an off-white solid. The perovskite was then obtained by heating stoichiometric amounts of the iodide salt with tin or lead iodide in an HI solution for 1 day before cooling.\",Single-crystal X-ray diffraction,A Bruker D8 Venture diffractometer with Mo Kalpha radiation was used. SAINT and SADABS in the APEX 3 software package was used for data reduction and absorption correction. The structure was solved using SHELXS and further refinement using SHELXL-2014 in the WINGX environment.\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead bromide\",C6H10N2Pb2Br6,\"(dmpz)[Pb2Br6], N,N‚Ä≤-dimethylpyrazinium hexabromo diplumbate(II)\",C6H10N2,\"Pb2Br6, Lead bromide\",\"N,N′-dimethylpyrazinium lead bromide\",3,powder,,,,,,,,\"PbBr2, HBr, pyrazine, MeOH\",dark red plate-shaped crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80ºC. After 24 hours, crystals began to precipitate.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. Wavelength used was λ = 0.7749 Å.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead bromide\",C6H10N2Pb2Br6,\"(dmpz)[Pb2Br6], N,N‚Ä≤-dimethylpyrazinium hexabromo diplumbate(II)\",C6H10N2,\"Pb2Br6, Lead bromide\",\"N,N′-dimethylpyrazinium lead bromide\",3,powder,,,,,,,,\"PbBr2, HBr, pyrazine, MeOH\",dark red plate-shaped crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80ºC. After 24 hours, crystals began to precipitate.\",UV-vis absorption (diffused reflectance),\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (α/S)^{2}, where α = absorption coefficient and S = scattering coefficient.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead bromide\",C6H10N2Pb2Br6,\"(dmpz)[Pb2Br6], N,N‚Ä≤-dimethylpyrazinium hexabromo diplumbate(II)\",C6H10N2,\"Pb2Br6, Lead bromide\",\"N,N′-dimethylpyrazinium lead bromide\",3,powder,,,,,,,,\"PbBr2, HBr, pyrazine, MeOH\",dark red plate-shaped crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80ºC. After 24 hours, crystals began to precipitate.\",EPR,\"A Bruker EMX spectrometer, an ER 041 XG microwave bridge, and an ER4116DM cavity were used at 77 K, frequency ~9.6 GHz, and a sweep time of 30 seconds.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead bromide\",C6H10N2Pb2Br6,\"(dmpz)[Pb2Br6], N,N‚Ä≤-dimethylpyrazinium hexabromo diplumbate(II)\",C6H10N2,\"Pb2Br6, Lead bromide\",\"N,N′-dimethylpyrazinium lead bromide\",3,powder,,,,,,,,\"PbBr2, HBr, pyrazine, MeOH\",dark red plate-shaped crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80ºC. After 24 hours, crystals began to precipitate.\",UV-vis absorption (diffused reflectance),\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\"\r\n10.1002/anie.202005012,N-Hydro-N′-methylpyrazinium lead bromide iodide,C5H8N2Pb2Br4.5I1.5,\"(Hmpz)[Pb2Br4.5I1.5], bis(N-hydro-N‚Ä≤-methylpyrazinium) nonabromo triiodo tetraplumbate(II)\",C5H8N2,\"Pb2Br4.5I1.5, Lead bromide iodide\",N-hydro-N′-methylpyrazinium lead bromide iodide,3,powder,,,,,,,,\"PbBr2, HBr, (mpz)I\",dark red crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (mpz)I (55 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the solution was remained undisturbed at room temperature, until crystals were obtained at 2 hours.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. λ = 0.7749 Å.\"\r\n10.1002/anie.202005012,N-Hydro-N′-methylpyrazinium lead bromide iodide,C5H8N2Pb2Br4.5I1.5,\"(Hmpz)[Pb2Br4.5I1.5], bis(N-hydro-N‚Ä≤-methylpyrazinium) nonabromo triiodo tetraplumbate(II)\",C5H8N2,\"Pb2Br4.5I1.5, Lead bromide iodide\",N-hydro-N′-methylpyrazinium lead bromide iodide,3,powder,,,,,,,,\"PbBr2, HBr, (mpz)I\",dark red crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (mpz)I (55 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the solution was remained undisturbed at room temperature, until crystals were obtained at 2 hours.\",UV-vis absorbance,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (α/S)^{2}, where α = absorption coefficient and S = scattering coefficient.\"\r\n10.1002/anie.202005012,N-Hydro-N′-methylpyrazinium lead bromide iodide,C5H8N2Pb2Br4.5I1.5,\"(Hmpz)[Pb2Br4.5I1.5], bis(N-hydro-N‚Ä≤-methylpyrazinium) nonabromo triiodo tetraplumbate(II)\",C5H8N2,\"Pb2Br4.5I1.5, Lead bromide iodide\",N-hydro-N′-methylpyrazinium lead bromide iodide,3,powder,,,,,,,,\"PbBr2, HBr, (mpz)I\",dark red crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (mpz)I (55 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the solution was remained undisturbed at room temperature, until crystals were obtained at 2 hours.\",UV-vis absorbance,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\"\r\n10.1002/anie.202005012,N-Hydro-N′-ethylpyrazinium lead bromide,C6H10N2Pb2Br6,\"(Hepz)[Pb2Br6], N-hydro-N‚Ä≤-ethylpyrazinium hexabromo diplumbate(II)\",C6H10N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-ethylpyrazinium lead bromide,3,powder,,,,,,,,\"PbBr2, HBr, (epz)I\",dark red crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (epz)I (59 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, remained undisturbed at room temperature, and crystals were obtained within 2 hours.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. λ = 0.7749 Å.\"\r\n10.1002/anie.202005012,N-Hydro-N′-ethylpyrazinium lead bromide,C6H10N2Pb2Br6,\"(Hepz)[Pb2Br6], N-hydro-N‚Ä≤-ethylpyrazinium hexabromo diplumbate(II)\",C6H10N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-ethylpyrazinium lead bromide,3,powder,,,,,,,,\"PbBr2, HBr, (epz)I\",dark red crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (epz)I (59 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, remained undisturbed at room temperature, and crystals were obtained within 2 hours.\",UV-vis absorption,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (α/S)^{2}, where α = absorption coefficient and S = scattering coefficient.\"\r\n10.1002/anie.202005012,N-Hydro-N′-ethylpyrazinium lead bromide,C6H10N2Pb2Br6,\"(Hepz)[Pb2Br6], N-hydro-N‚Ä≤-ethylpyrazinium hexabromo diplumbate(II)\",C6H10N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-ethylpyrazinium lead bromide,3,powder,,,,,,,,\"PbBr2, HBr, (epz)I\",dark red crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (epz)I (59 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, remained undisturbed at room temperature, and crystals were obtained within 2 hours.\",UV-vis absorption,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\"\r\n10.1002/anie.202005012,N-Hydro-N′-isopropylpyrazinium lead bromide,C7H12N2Pb2Br6,\"(Hppz)[Pb2Br6], N-hydro-N‚Ä≤-isopropylpyrazinium hexabromo diplumbate(II)\",C7H12N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-isopropylpyrazinium lead bromide,3,powder,,,,,,,,\"PbBr2, HBr, (ppz)I\",dark red rhombic-plate crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. λ = 0.6888 Å.\"\r\n10.1002/anie.202005012,N-Hydro-N′-isopropylpyrazinium lead bromide,C7H12N2Pb2Br6,\"(Hppz)[Pb2Br6], N-hydro-N‚Ä≤-isopropylpyrazinium hexabromo diplumbate(II)\",C7H12N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-isopropylpyrazinium lead bromide,3,powder,,,,,,,,\"PbBr2, HBr, (ppz)I\",dark red rhombic-plate crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",UV-vis absorption,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (α/S)^{2}, where α = absorption coefficient and S = scattering coefficient.\"\r\n10.1002/anie.202005012,N-Hydro-N′-isopropylpyrazinium lead bromide,C7H12N2Pb2Br6,\"(Hppz)[Pb2Br6], N-hydro-N‚Ä≤-isopropylpyrazinium hexabromo diplumbate(II)\",C7H12N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-isopropylpyrazinium lead bromide,3,unknown,,,,,,,,\"PbBr2, HBr, (ppz)I\",dark red rhombic-plate crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",,\r\n10.1002/anie.202005012,N-Hydro-N′-isopropylpyrazinium lead bromide,C7H12N2Pb2Br6,\"(Hppz)[Pb2Br6], N-hydro-N‚Ä≤-isopropylpyrazinium hexabromo diplumbate(II)\",C7H12N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-isopropylpyrazinium lead bromide,3,bulk polycrystalline,,,,,,,,\"PbBr2, HBr, (ppz)I\",dark red rhombic-plate crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",Photoluminescence excitation,A Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector was used for emission and excitation spectra. FluorEssence 2.3.15 software was used to collect data.\r\n10.1002/anie.202005012,N-Hydro-N′-isopropylpyrazinium lead bromide,C7H12N2Pb2Br6,\"(Hppz)[Pb2Br6], N-hydro-N‚Ä≤-isopropylpyrazinium hexabromo diplumbate(II)\",C7H12N2,\"Pb2Br6, Lead bromide\",N-hydro-N′-isopropylpyrazinium lead bromide,3,powder,,,,,,,,\"PbBr2, HBr, (ppz)I\",dark red rhombic-plate crystals,\"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\"\r\n10.1002/anie.202005012,\"N,N′-Dihydro-3-amidinopyridinium lead bromide\",C6H9N3Pb2Br6,\"(H2apy)[Pb2Br6], N,N‚Ä≤-dihydro-3-amidinopyridinium hexabromo diplumbate(II)\",C6H9N3,\"Pb2Br6, Lead bromide\",\"N,N′-dihydro-3-amidinopyridinium lead bromide\",3,powder,,,,,,,,\"PbBr2, 3-amidinopyridine hydrobromide, HBr\",pale yellow plate-shaped crystals,\"First, solid PbBr2 (196 mg, 0.534 mmol) and 3-amidinopyridine hydrobromide (40.5 mg, 0.200 mmol) were combined. HBr aq. (9 M, 2.0 mL) was added to the mixture, and a yellow solution formed. The solution was heated to 100ºC for 4 hours. Then, the solution cooled at a constant rate of 5ºC per hour, obtaining the crystals.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. λ = 0.7288 Å.\"\r\n10.1002/anie.202005012,\"N,N′-Dihydro-3-amidinopyridinium lead bromide\",C6H9N3Pb2Br6,\"(H2apy)[Pb2Br6], N,N‚Ä≤-dihydro-3-amidinopyridinium hexabromo diplumbate(II)\",C6H9N3,\"Pb2Br6, Lead bromide\",\"N,N′-dihydro-3-amidinopyridinium lead bromide\",3,unknown,,,,,,,,\"PbBr2, 3-amidinopyridine hydrobromide, HBr\",pale yellow plate-shaped crystals,\"First, solid PbBr2 (196 mg, 0.534 mmol) and 3-amidinopyridine hydrobromide (40.5 mg, 0.200 mmol) were combined. HBr aq. (9 M, 2.0 mL) was added to the mixture, and a yellow solution formed. The solution was heated to 100ºC for 4 hours. Then, the solution cooled at a constant rate of 5ºC per hour, obtaining the crystals.\",Photoluminescence,A Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector was used for emission and excitation spectra. FluorEssence 2.3.15 software was used to collect data.\r\n10.1002/anie.202005012,\"N,N′-Dihydro-3-amidinopyridinium lead bromide\",C6H9N3Pb2Br6,\"(H2apy)[Pb2Br6], N,N‚Ä≤-dihydro-3-amidinopyridinium hexabromo diplumbate(II)\",C6H9N3,\"Pb2Br6, Lead bromide\",\"N,N′-dihydro-3-amidinopyridinium lead bromide\",3,powder,,,,,,,,\"PbBr2, 3-amidinopyridine hydrobromide, HBr\",pale yellow plate-shaped crystals,\"First, solid PbBr2 (196 mg, 0.534 mmol) and 3-amidinopyridine hydrobromide (40.5 mg, 0.200 mmol) were combined. HBr aq. (9 M, 2.0 mL) was added to the mixture, and a yellow solution formed. The solution was heated to 100ºC for 4 hours. Then, the solution cooled at a constant rate of 5ºC per hour, obtaining the crystals.\",UV-vis absorption,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\"\r\n10.1002/anie.202005012,\"N,N′-Dihydro-1,3-propanediammonium lead bromide\",C3H12N2Pb2Br6,\"(H2dap)[Pb2Br6], N,N‚Ä≤-dihydro-1,3-propanediammonium hexabromo diplumbate(II)\",C3H12N2,\"Pb2Br6, Lead bromide\",\"N,N′-dihydro-1,3-propanediammonium lead bromide\",3,powder,,,,,,,,,,,,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. λ = 0.71073 Å.\"\r\n10.1002/anie.202005012,\"N,N′-Dihydro-1,3-propanediammonium lead bromide\",C3H12N2Pb2Br6,\"(H2dap)[Pb2Br6], N,N‚Ä≤-dihydro-1,3-propanediammonium hexabromo diplumbate(II)\",C3H12N2,\"Pb2Br6, Lead bromide\",\"N,N′-dihydro-1,3-propanediammonium lead bromide\",3,powder,,,,,,,,\"PbBr2, 1,2-dap, HBr\",colorless needle-like crystals,\"First, solid PbBr2 (171 mg, 0.465 mmol) and liquid 1,2-dap (13.2 μL, 0.157 mmol) were added, in a 3:1 ratio, in HBr aq. Solution (4.45 M, 0.7 mL). The solution was heated to 100ºC and stirred. The solution then cooled to room temperature at a rate of 3ºC per hour, the precipitate was dried under reduced pressure for 12 hours, and crystals were obtained.\",UV-vis absorption,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead iodide\",C6H10N2Pb2I6,\"(dmpz)[Pb2I6],N, N‚Ä≤-dimethylpyrazinium hexaiodo diplumbate(II)\",C6H10N2,\"Pb2I6, Lead iodide\",\"N, N′-dimethylpyrazinium lead iodide\",3,unknown,,,,,,,,\"PbI2, NaI, GBL, dmpz(BF4)2\",opaque black plate-shaped crystals,\"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. λ = 0.7288 Å.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead iodide\",C6H10N2Pb2I6,\"(dmpz)[Pb2I6],N, N‚Ä≤-dimethylpyrazinium hexaiodo diplumbate(II)\",C6H10N2,\"Pb2I6, Lead iodide\",\"N, N′-dimethylpyrazinium lead iodide\",3,film,,,,,,,,\"PbI2, NaI, GBL, dmpz(BF4)2\",opaque black plate-shaped crystals,\"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead iodide\",C6H10N2Pb2I6,\"(dmpz)[Pb2I6],N, N‚Ä≤-dimethylpyrazinium hexaiodo diplumbate(II)\",C6H10N2,\"Pb2I6, Lead iodide\",\"N, N′-dimethylpyrazinium lead iodide\",3,powder,,,,,,,,\"PbI2, NaI, GBL, dmpz(BF4)2\",opaque black plate-shaped crystals,\"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead iodide\",C6H10N2Pb2I6,\"(dmpz)[Pb2I6],N, N‚Ä≤-dimethylpyrazinium hexaiodo diplumbate(II)\",C6H10N2,\"Pb2I6, Lead iodide\",\"N, N′-dimethylpyrazinium lead iodide\",3,powder,,,,,,,,\"PbI2, NaI, GBL, dmpz(BF4)2\",opaque black plate-shaped crystals,\"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",UV-vis absorbance,\"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (α/S)^{2}, where α = absorption coefficient and S = scattering coefficient.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead iodide\",C6H10N2Pb2I6,\"(dmpz)[Pb2I6],N, N‚Ä≤-dimethylpyrazinium hexaiodo diplumbate(II)\",C6H10N2,\"Pb2I6, Lead iodide\",\"N, N′-dimethylpyrazinium lead iodide\",3,pellet,,,,,,,,\"PbI2, NaI, GBL, dmpz(BF4)2\",opaque black plate-shaped crystals,\"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",Conductivity,\"Powder was dehydrated under reduced pressure and pressed into circular pellets. Conductivity was measured on the pellets by using a Bio-Logic VSP300 Potentiostat/Galvanostat. Cyclic voltagramms vs. open circuit potential were found, a best fit line was generated to find resistance, and conductivity was found by σ=1/ρ, where ρ = (wtR)/L.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead iodide\",C6H10N2Pb2I6,\"(dmpz)[Pb2I6],N, N‚Ä≤-dimethylpyrazinium hexaiodo diplumbate(II)\",C6H10N2,\"Pb2I6, Lead iodide\",\"N, N′-dimethylpyrazinium lead iodide\",3,pellet,,,,,,,,\"PbI2, NaI, GBL, dmpz(BF4)2\",opaque black plate-shaped crystals,\": First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",Conductivity,\"Powder was dehydrated under reduced pressure and pressed into circular pellets. Conductivity was measured on the pellets by using a Bio-Logic VSP300 Potentiostat/Galvanostat. Cyclic voltagramms vs. open circuit potential were found, a best fit line was generated to find resistance, and conductivity was found by σ=1/ρ, where ρ = (wtR)/L.\"\r\n10.1002/anie.202005012,\"N, N′-Dimethylpyrazinium lead iodide\",C6H10N2Pb2I6,\"(dmpz)[Pb2I6],N, N‚Ä≤-dimethylpyrazinium hexaiodo diplumbate(II)\",C6H10N2,\"Pb2I6, Lead iodide\",\"N, N′-dimethylpyrazinium lead iodide\",3,powder,,,,,,,,\"PbI2, NaI, GBL, dmpz(BF4)2\",opaque black plate-shaped crystals,\"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",,\"Powder was dehydrated under reduced pressure and pressed into circular pellets. Conductivity was measured on the pellets by using a Bio-Logic VSP300 Potentiostat/Galvanostat. Cyclic voltagramms vs. open circuit potential were found, a best fit line was generated to find resistance, and conductivity was found by σ=1/ρ, where ρ = (wtR)/L.\"\r\n10.1002/anie.202215206,4-(R)-(+)-β-methylphenethylammonium indium antimony chloride,C36H52N4In0.89Sb1.11Cl10,\"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-β-methylphenethylamine)4In2(1-x)Sb2xCl10\",C9H13N,In0.89Sb1.11Cl10,(R)-(+)-β-methylphenethylaminium indium antimony chloride,0,single crystal,,,,,,,,\"In2O3, MPA, HCl\",Single crystals of 4-(R)-(+)-β-methylphenethylamine indium antimony chloride,\"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 μL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling.\",Single-crystal X-ray diffraction,\"Atomic structure data was collected on a Bruker D8 Venture diffractometer with Mo-Kα radiation of λ = 0.71073 Å at 173 Kelvin. Bruker software (APEX3), Olex2, and SHELXL methods were used in data reduction and structure analysis.\"\r\n10.1002/anie.202215206,4-(R)-(+)-β-methylphenethylammonium indium antimony chloride,C36H52N4In0.89Sb1.11Cl10,\"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-β-methylphenethylamine)4In2(1-x)Sb2xCl10\",C9H13N,In0.89Sb1.11Cl10,(R)-(+)-β-methylphenethylaminium indium antimony chloride,0,powder,,,,,,,,\"In2O3, MPA, HCl\",Powder of 4-(R)-(+)-β-methylphenethylamine indium antimony chloride,\"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 μL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling. For UV-vis spectroscopy, these single crystals were then ground into a powder.\",UV-vis spectroscopy,\"UV-vis spectroscopy was employed to record the absorbance of powder samples of the crystal, which were adhered onto a barium sulfate (BaSO4) background. A UH5700 spectrophotometer with a 60 mm diameter integrating sphere measured data between 200 - 600 nm wavelength. Such data was then plotted using the Kubelka-Munk equation: α/S = [(1−R)^2]/2R, with α being the absorption coefficient, S being the scattering coefficient, and R representing absolute reflectance.\"\r\n10.1002/anie.202215206,4-(R)-(+)-β-methylphenethylammonium indium antimony chloride,C36H52N4In0.89Sb1.11Cl10,\"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-β-methylphenethylamine)4In2(1-x)Sb2xCl10\",C9H13N,In0.89Sb1.11Cl10,(R)-(+)-β-methylphenethylaminium indium antimony chloride,0,single crystal,,,,,,,,\"In2O3, MPA, HCl\",Single crystals of 4-(R)-(+)-β-methylphenethylamine indium antimony chloride,\"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 μL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling.\",PL spectroscopy,PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution). The excitation wavelength was 350 nm.\r\n10.1002/anie.202215206,4-(R)-(+)-β-methylphenethylammonium indium antimony chloride,C36H52N4In0.89Sb1.11Cl10,\"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-β-methylphenethylamine)4In2(1-x)Sb2xCl10\",C9H13N,In0.89Sb1.11Cl10,(R)-(+)-β-methylphenethylaminium indium antimony chloride,0,single crystal,,,,,,,,\"In2O3, MPA, HCl\",Single crystals of 4-(R)-(+)-β-methylphenethylamine indium antimony chloride,\"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 μL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling.\",PL spectroscopy,\"PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution). For this material, the emission wavelength was 650 nm.\"\r\n10.1002/anie.202215206,4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,C32H72N4In1.64Sb0.36Cl10,(R-CHEA)4In1.64Sb0.36Cl10,C8H18N,In1.64Sb0.36Cl10,(R)-(−)-1-cyclohexylethylaminium indium antimony chloride,0,single crystal,,,,,,,,\"CHEA, In2O3, HCl\",Single crystals of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,\"CHEA (1 mmol, 146 μL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90°Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1°C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50°C in a vacuum oven.\",Single-crystal X-ray diffraction (SC-XRD),\"SC-XRD data was collected via a Bruker D8 Venture diffractometer. Mo-Kα radiation occurred at 173 K with λ = 0.71073 Å. Bruker APEX3, Olex2, and SHELXL software were used for further analysis.\"\r\n10.1002/anie.202215206,4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,C32H72N4In1.64Sb0.36Cl10,(R-CHEA)4In1.64Sb0.36Cl10,C8H18N,In1.64Sb0.36Cl10,(R)-(−)-1-cyclohexylethylaminium indium antimony chloride,0,powder,,,,,,,,\"CHEA, In2O3, HCl\",Powder of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,\"CHEA (1 mmol, 146 μL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90°Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1°C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50°C in a vacuum oven. For UV-vis spectroscopy, these single crystals were then ground into a powder.\",UV-vis spectroscopy,\"UV-vis spectroscopy was employed to record the absorbance of powder samples of the crystal, which were adhered onto a barium sulfate (BaSO4) background. A UH5700 spectrophotometer with a 60 mm diameter integrating sphere measured data between 200 - 600 nm wavelength. Such data was then plotted using the Kubelka-Munk equation: α/S = [(1−R)^2]/2R, with α being the absorption coefficient, S being the scattering coefficient, and R representing absolute reflectance.\"\r\n10.1002/anie.202215206,4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,C32H72N4In1.64Sb0.36Cl10,(R-CHEA)4In1.64Sb0.36Cl10,C8H18N,In1.64Sb0.36Cl10,(R)-(−)-1-cyclohexylethylaminium indium antimony chloride,0,single crystal,,,,,,,,\"CHEA, In2O3, HCl\",Single crystals of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,\"CHEA (1 mmol, 146 μL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90°Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1°C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50°C in a vacuum oven.\",PL spectroscopy,\"PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution). For this material, the emission wavelength was 710 nm.\"\r\n10.1002/anie.202215206,4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,C32H72N4In1.64Sb0.36Cl10,(R-CHEA)4In1.64Sb0.36Cl10,C8H18N,In1.64Sb0.36Cl10,(R)-(−)-1-cyclohexylethylaminium indium antimony chloride,0,single crystal,,,,,,,,\"CHEA, In2O3, HCl\",Single crystals of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride,\"CHEA (1 mmol, 146 μL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90°Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1°C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(−)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50°C in a vacuum oven.\",PL spectroscopy,PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution) at a 350 nm wavelength.\r\n10.1002/chem.201505055,tris(methylammonium) bismuth iodide,C3H18N3Bi2I9,\"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",CH6N,\"Bi2I9, Bismuth iodide\",tris(methanaminium) bismuth iodide,0,powder,VASP,DFT,GGA-PBE + SO,,,PAW,,N/A,,\"Solution-assisted MBI was placed on borosilicate glass and quartz substrates, which were cleaned ultrasonically and with oxygen plasma. A solution of BiI3 was prepared by dissolving BiI3 (200 mg) in 0.5 mL DMF. This solution was mixed for one hour before being filtered through a 0.2 μm PTFEsyringe filter. Next, 10μL of the filtered solution was spread on a substrate, spin-cast (3000 rpm for 5s, 6000 rpm for 5s). BiI¬3 film was dried for 30 minutes and annealed at 100ºC for half an hour. In the meantime, methylammonium iodide was dissolved in anhydrous isopropanol (6 mg mL-1). 200 μL of methylammonium iodide was then deposited on the BiI3 film for one minute before spinning and finally being annealed at 100ºC for 1 hour.\",PXRD,Rietveld refinement. Powder X-Ray diffraction was performed with a PANanalytical X’Pert PRO XRPD using Cu Kα radiation (1.5406 Å). PXRD of MBI was performed by grazing incident X-ray diffraction (GIXD) using Rigaku SmartLab using Cu Kα radiation (1.5406 Å wavelength) and incident angle 0.5º.\r\n10.1002/chem.201505055,tris(methylammonium) bismuth iodide,C3H18N3Bi2I9,\"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",CH6N,\"Bi2I9, Bismuth iodide\",tris(methanaminium) bismuth iodide,0,film,,,,,,,,\"BiI3 (99.999%, Alfa Aesar), N, N-Dimethylformamide (DMF, Sigma-Aldrich), Methylammonium iodide (MAI, Luminescence Technology Corp.),\",film on quartz substrates,\"200 mg BiI3 powder was dissolved in 0.5 mL DMF. 20 μL of this solution was heated at 150 °C on a hotplate for 30 s. The solution was then spin-coated at 4000 rpm for 10 s. The film was annealed at 100 °C. The film was kept over MAI powder heated at 150 °C for 4 hr under vacuum. The film was then cooled to room temperature and was washed with anhydrous isopropanol. Finally, it was annealed for 1 hr at 100 °C in a nitrogen-filled glovebox.\",Photoluminescence with integrating sphere,\"PL quantum efficiency measurements were performed using an integrating sphere (Labsphere RTC-060-\r\nSF). A 405 nm wavelength diode laser as excitation source, and a 535 nm longpass Schott glass filter.\"\r\n10.1002/chem.201505055,tris(methylammonium) bismuth iodide,C3H18N3Bi2I9,\"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",CH6N,\"Bi2I9, Bismuth iodide\",tris(methanaminium) bismuth iodide,0,film,,,,,,,,\"BiI3 (99.999%, Alfa Aesar), N, N-Dimethylformamide (DMF, Sigma-Aldrich), Methylammonium iodide (MAI, Luminescence Technology Corp.)\",film on quartz substrates,\"200 mg BiI3 powder was dissolved in 0.5 mL DMF. The solution was filtered through a 0.2 μm PTFE syringe filter. 10 μL of the solution was spin-coated at 3000 rpm for 5 s, followed by 6000 rpm for 5 s. The film was dried for 30 min and was annealed at 100 °C for 30 min. an MAI solution of concentration of 6 mg·mL-1in anhydrous isopropanol was prepared.  200 μL of MAI solution was kept on the BiI3 film for 60 s. The film was then spun at 4000 rpm for 20 s. The film was finally annealed at 100 °C for 1 hr.\",Photoluminescence,\"Photoluminescence spectra were acquired using a FluoroMax-3, excitation wavelength of 360 nm, and slit size of 5 nm\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead iodide,Pb2I(SC6H5)3,Tris(thiophenyl) monoiododiplumbate(II),SC6H5,\"Pb2I, Lead iodide\",Tris(thiophenyl) lead iodide,2,single crystal,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium ioddie (MAI), N, N-dimethylformamide (DMF)\",orange plate-shaped crystals,\"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.Pb(SC6H5)2 (107 mg) and MAI (40 mg) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95ºC, at which temperature the stirring stopped and the solution was cooled at a rate of 5ºC per 20 minutes until the temperature reached 40ºC. The solution was left, undisturbed, overnight.\",Single crystal X-ray diffraction,Bruker AXS D8 Quest CMOS diffractometer with Mo Kα radiation (λ = 0.71073 Å) was used. Frames were collected at 150 K with ω and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\r\n10.1002/chem.201905790,Tris(thiophenyl) lead iodide,Pb2I(SC6H5)3,Tris(thiophenyl) monoiododiplumbate(II),SC6H5,\"Pb2I, Lead iodide\",Tris(thiophenyl) lead iodide,2,nanoform,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium iodide (MAI), N, N-dimethylformamide (DMF), ethanol\",exfoliated crystals on silicon substrates,\"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.\r\nPb(SC6H5)2 (107 mg) and MAI (40 mg) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95ºC, at which temperature the stirring stopped and the solution was cooled at a rate of 5ºC per 20 minutes until the temperature reached 40ºC. The solution was left, undisturbed, overnight. The crystals were washed with ethanol. Exfoliation was performed using scotch tape.\",Photoluminescence microscopy,\"Two independent sub-picosecond excitation beams (400 nm) were generated by two optical parametric amplifiers. Beams were focused onto a sample with 40X objective, PL emission was collected with the same objective (Nikon, NA = 0.6), dispersed by a 300 mm spectrometer (Andor Tech.), and detected by a thermoelectric cooled CCD detector.\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead iodide,Pb2I(SC6H5)3,Tris(thiophenyl) monoiododiplumbate(II),SC6H5,\"Pb2I, Lead iodide\",Tris(thiophenyl) lead iodide,2,nanoform,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium iodide (MAI), N, N-dimethylformamide (DMF), ethanol\",\"exfoliated crystals on silicon substrates (for PL)\r\n+ thin film on quartz substrates (for absorption)\",,Photoluminescence microscopy + UV-vis absorption (transmission mode),\r\n10.1002/chem.201905790,Tris(thiophenyl) lead iodide,Pb2I(SC6H5)3,Tris(thiophenyl) monoiododiplumbate(II),SC6H5,\"Pb2I, Lead iodide\",Tris(thiophenyl) lead iodide,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",Thin film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),\"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead iodide,Pb2I(SC6H5)3,Tris(thiophenyl) monoiododiplumbate(II),SC6H5,\"Pb2I, Lead iodide\",Tris(thiophenyl) lead iodide,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",Thin film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70ºC in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. \r\nThin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),\"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with a direct band gap assumption.\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead iodide,Pb2I(SC6H5)3,Tris(thiophenyl) monoiododiplumbate(II),SC6H5,\"Pb2I, Lead iodide\",Tris(thiophenyl) lead iodide,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (!0 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra.\r\n10.1002/chem.201905790,Tris(thiophenyl) lead iodide,Pb2I(SC6H5)3,Tris(thiophenyl) monoiododiplumbate(II),SC6H5,\"Pb2I, Lead iodide\",Tris(thiophenyl) lead iodide,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra.\r\n10.1002/chem.201905790,Tris(thiophenyl) lead bromide,Pb2Br(SC6H5)3,Tris(thiophenyl) monobromodiplumbate(II),SC6H5,\"Pb2Br, Lead bromide\",Tris(thiophenyl) lead bromide,2,single crystal,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium bromide (MABr), N, N-dimethylformamide (DMF)\",Orange plate-like crystals,\"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.Pb(SC6H5)2 (107 mg) and MABr (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95ºC, at which temperature the stirring stopped and the solution was cooled at a rate of 5ºC per 20 minutes until the temperature reached 40ºC. The solution was left, undisturbed, overnight.\",Single crystal X-ray diffraction,Bruker AXS D8 Quest CMOS diffractometer with Mo Kα radiation (λ = 0.71073 Å) was used. Frames were collected at 150 K with ω and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\r\n10.1002/chem.201905790,Tris(thiophenyl) lead bromide,Pb2Br(SC6H5)3,Tris(thiophenyl) monobromodiplumbate(II),SC6H5,\"Pb2Br, Lead bromide\",Tris(thiophenyl) lead bromide,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead bromide (PbBr2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. \r\n\r\nThin films were created by mixing Pb(SC6H5)2 and PbBr2 in a 3:1 ratio in DMF and 0.9 mL DMSO. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption,A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra. Images were obtained via a Hitachi 4600-S scanning electron microscope\r\n10.1002/chem.201905790,Tris(thiophenyl) lead bromide,Pb2Br(SC6H5)3,Tris(thiophenyl) monobromodiplumbate(II),SC6H5,\"Pb2Br, Lead bromide\",Tris(thiophenyl) lead bromide,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead bromide (PbBr2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbBr2 in a 3:1 ratio in DMF and 0.9 mL DMSO. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),\"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead bromide,Pb2Br(SC6H5)3,Tris(thiophenyl) monobromodiplumbate(II),SC6H5,\"Pb2Br, Lead bromide\",Tris(thiophenyl) lead bromide,2,nanoform,,,,,,,,\"lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium bromide (MABr), N, N-dimethylformamide (DMF), ethanol\",exfoliated crystals on silicon substrates,\"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.\r\nPb(SC6H5)2 (107 mg) and MABr (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95ºC, at which temperature the stirring stopped and the solution was cooled at a rate of 5ºC per 20 minutes until the temperature reached 40ºC. The solution was left, undisturbed, overnight.\",Photoluminescence microscopy,\"Two independent sub-picosecond excitation beams (400 nm) were generated by two optical parametric amplifiers. Beams were focused onto a sample with 40X objective, PL emission was collected with the same objective (Nikon, NA = 0.6), dispersed by a 300 mm spectrometer (Andor Tech.), and detected by a thermoelectric cooled CCD detector.\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead bromide,Pb2Br(SC6H5)3,Tris(thiophenyl) monobromodiplumbate(II),SC6H5,\"Pb2Br, Lead bromide\",Tris(thiophenyl) lead bromide,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead bromide (PbBr2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbBr2 in a 3:1 ratio in DMF and 0.9 mL DMSO. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data.\r\n10.1002/chem.201905790,Tris(thiophenyl) lead chloride,Pb2Cl(SC6H5)3,Tris(thiophenyl) monochlorodiplumbate(II),SC6H5,\"Pb2Cl, Lead chloride\",Tris(thiophenyl) lead chloride,2,single crystal,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium chloride (MACl), N, N-dimethylformamide (DMF)\",Orange plate-like crystals,\"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.Pb(SC6H5)2 (107 mg) and MACl (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95ºC, at which temperature the stirring stopped and the solution was cooled at a rate of 5ºC per 20 minutes until the temperature reached 40ºC. The solution was left, undisturbed, overnight.\",Single crystal X-ray diffraction,Bruker AXS D8 Quest CMOS diffractometer with Mo Kα radiation (λ = 0.71073 Å) was used. Frames were collected at 150 K with ω and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\r\n10.1002/chem.201905790,Tris(thiophenyl) lead chloride,Pb2Cl(SC6H5)3,Tris(thiophenyl) monochlorodiplumbate(II),SC6H5,\"Pb2Cl, Lead chloride\",Tris(thiophenyl) lead chloride,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead chloride (PbCl2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbCl2 in a 3:1 ratio in DMF and 0.9 mL DMSO. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra. Images were obtained via a Hitachi 4600-S scanning electron microscope\r\n10.1002/chem.201905790,Tris(thiophenyl) lead chloride,Pb2Cl(SC6H5)3,Tris(thiophenyl) monochlorodiplumbate(II),SC6H5,\"Pb2Cl, Lead chloride\",Tris(thiophenyl) lead chloride,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead chloride (PbCl2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbCl2 in a 3:1 ratio in DMF and 0.9 mL DMSO. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),\"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead chloride,Pb2Cl(SC6H5)3,Tris(thiophenyl) monochlorodiplumbate(II),SC6H5,\"Pb2Cl, Lead chloride\",Tris(thiophenyl) lead chloride,2,nanoform,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium chloride (MACl), N, N-dimethylformamide (DMF)\",exfoliated crystals on silicon substrates,\"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.\r\nPb(SC6H5)2 (107 mg) and MACl (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95ºC, at which temperature the stirring stopped and the solution was cooled at a rate of 5ºC per 20 minutes until the temperature reached 40ºC. The solution was left, undisturbed, overnight. The crystals were washed with ethanol. Exfoliation was performed using scotch tape.\",Photoluminescence microscopy,\"Two independent sub-picosecond excitation beams (400 nm) were generated by two optical parametric amplifiers. Beams were focused onto a sample with 40X objective, PL emission was collected with the same objective (Nikon, NA = 0.6), dispersed by a 300 mm spectrometer (Andor Tech.), and detected by a thermoelectric cooled CCD detector.\"\r\n10.1002/chem.201905790,Tris(thiophenyl) lead chloride,Pb2Cl(SC6H5)3,Tris(thiophenyl) monochlorodiplumbate(II),SC6H5,\"Pb2Cl, Lead chloride\",Tris(thiophenyl) lead chloride,2,film,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead chloride (PbCl2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",Thin-film on quartz,\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70º in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbCl2 in a 3:1 ratio in DMF and 0.9 mL DMSO. 40 μL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 μL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100ºC for 5 min.\",UV-vis absorption (transmission mode),The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data.\r\n10.1002/chem.201905790,PbI1.524(S-C6H5)0.476,PbI1.524(S-C6H5)0.476,*,SC6H5,Lead iodide,*,2,single crystal,,,,,,,,\"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium iodide (MAI), ethanol, γ-butyrolactone (GBL)\",\"dark orange, plate-shaped crystals\",\"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (!0 mL) while being simultaneously heated at 70º C in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. \r\n\r\nSingle crystals were grown via vapor diffusion. A 1:4 molar ratio of Pb(SC6H5)2 and MAI were dissolved in γ- butyrolactone (GBL) and produced a 200 mg mL-1 solution by being heated and stirred for 1 hour.  0.3 mL was placed into a small vial, then into a larger vial with 5 mL of ethanol, and sealed for three days, at which time crystals formed.\",Single crystal X-ray diffraction,Bruker AXS D8 Quest CMOS diffractometer with Mo Kα radiation (λ = 0.71073 Å) was used. Frames were collected at 150 K with ω and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\r\n10.1002/chem.201905790,PbI1.524(S-C6H5)0.476,PbI1.524(S-C6H5)0.476,*,SC6H5,Lead iodide,*,2,film,,,,,,,,,,,UV-vis absorption (transmission mode),\"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\"\r\n10.1006/jssc.1995.1023,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,powder,,,,,,,,\"Tin (II) oxide, HI (aq), ethylene glycol, argon, nitrogen\",Black-green powder.,\"Dissolve Tin (II) oxide (10.40 g, 27.9 mmole) in 20 ml of a concentrate (57% by weight) HI (aq) in a test tube under flowing argon. \r\n\r\nAdd another 8.0 ml of aqueous HI to a test tube containing CH3NH3-HI (4.44g, 27.9 mmole). \r\n\r\nGently heat solution to 90.0 °C in a water/ethylene glycol bath to facilitate dissolution. Mix warm CH3NH2-HI and SNI2 solutions and cool the resulting yellow solution to room temperature.\r\n\r\nFilter the black-green precipitate that forms under flowing nitrogen and dry under flowing argon at 100 °C for 5 hr. Yield is typically 76 %. CH3NH3SnI3 is air sensitive and decomposes in air within several hours. All samples are stored and manipulated for the various measurements in an argon-filled glove box with oxygen and water levels below 1 ppm.\",Powder X-ray diffraction,Not specified. Refer to Page 160 Experimental paragraph 1.\r\n10.1006/jssc.1995.1023,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,single crystal,,,,,,,,\"Tin (II) oxide, HI (aq), ethylene glycol, argon, nitrogen\",Black single crystal,\"Dissolve Tin (II) oxide (10.40 g, 27.9 mmole) in 20 ml of a concentrate (57% by weight) HI (aq) in a test tube under flowing argon. \r\n\r\nAdd another 8.0 ml of aqueous HI to a test tube containing CH3NH3-HI (4.44g, 27.9 mmole). \r\n\r\nGently heat solution to 90.0 °C in a water/ethylene glycol bath to facilitate dissolution. Mix warm CH3NH2-HI and SNI2 solutions and cool the resulting yellow solution to room temperature.\r\n\r\nFilter the black-green precipitate that forms under flowing nitrogen and dry under flowing argon at 100 °C for 5 hr. Yield is typically 76 %. CH3NH3SnI3 is air sensitive and decomposes in air within several hours. All samples are stored and manipulated for the various measurements in an argon-filled glove box with oxygen and water levels below 1 ppm.\r\n\r\nUse 2.0 g of CH3NH3SnI3 and equilibrate at 90.0 °C in a water/ethylene glycol bath. Add sufficient HI under flowing argon to dissolve the entire charge (about 11 ml). Cool the solution to -10.0 °C at 2 °C/hr. The small black crystals grow in a rhombic dodecahedral habit.\",X-ray diffraction,\"Not specified. Refer to Page 160 Experimental paragraph 1,3.\"\r\n10.1006/jssc.1997.7593,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,powder,,,,,,,,\"Tin (II) iodide, methylammonium iodide, HI (aq), argon, nitrogen\",Powder,\"Dissolve tin(II) iodide (2.235 g, 6 mmol) in flowing argon at 70°C in 4 ml of a concentrated (57% by weight) aqueous HI solution. \r\n\r\nDissolve methylammonium iodide (6 mmol) at room temperature in 1.0 ml of concentrated aqueous hydriodic acid and immediately add to the tin(II) iodide solution (after allowing it to cool). \r\n\r\nRinse the methylammonium tube using two additional 0.5-ml portions of hydriodic acid and add to the test tube containing the product, which at all times was kept in an inert atmosphere of flowing argon.\r\n\r\nMaintain the product in the hydriodic acid solution for 15 min at room temperature, with periodic agitation of the solution, and filter under flowing dry nitrogen gas.\r\n\r\nDry powder under vacuum at room temperature and store in an argon-filled glovebox, with oxygen and water levels maintained below 1 ppm.\",Powder X-ray diffraction,\"Siemens D5000 CuKα radiation, refined using Siemens WIN-METRIC program. Refer to Page 377 X-ray diffraction section.\"\r\n10.1006/jssc.1997.7593,Formamidinium tin iodide,CH5N2SnI3,\"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",CH5N2,\"SnI3, Tin iodide\",Imidoformamidinium tin (II) iodide,3,powder,,,,,,,,\"Tin (II) iodide, formamidine acetate, HI (aq), argon, nitrogen\",Black powder,\"Dissolve tin(II) iodide (2.235 g, 6 mmol) in flowing argon at 70°C in 4 ml of a concentrated (57% by weight) aqueous HI solution. \r\n\r\nDissolve formamidine acetate (0.6246 g, 6 mmol) at room temperature in 1.0 ml of concentrated aqueous hydriodic acid and immediately add to the tin(II) iodide solution (after allowing it to cool), leading to a thick black precipitate. \r\n\r\nRinse the formamidinium tube using two additional 0.5-ml portions of hydriodic acid and add to the test tube containing the product, which at all times was kept in an inert atmosphere of flowing argon.\r\n\r\nMaintain the product in the hydriodic acid solution for 15 min at room temperature, with periodic agitation of the solution, and filter under flowing dry nitrogen gas.\r\n\r\nYield was approximately 75% of the theoretical yield. Dry black powder under vacuum at room temperature and store in an argon-filled glovebox, with oxygen and water levels maintained below 1 ppm.\",Powder X-ray diffraction,\"Siemens D5000 CuKalpha radiation, refined using Siemens WIN-METRIC program. Refer to Page 377 X-ray diffraction section.\"\r\n10.1006/jssc.1997.7593,Formamidinium tin iodide,CH5N2SnI3,\"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",CH5N2,\"SnI3, Tin iodide\",Imidoformamidinium tin (II) iodide,3,single crystal,,,,,,,,\"Tin (II) iodide, formamidine acetate, HI (aq), argon, nitrogen\",Black single crystal,\"Dissolve tin(II) iodide (2.235 g, 6 mmol) in flowing argon at 70°C in 4 ml of a concentrated (57% by weight) aqueous HI solution. \r\n\r\nDissolve formamidine acetate (0.6246 g, 6 mmol) at room temperature in 1.0 ml of concentrated aqueous hydriodic acid and immediately add to the tin(II) iodide solution (after allowing it to cool), leading to a thick black precipitate. \r\n\r\nRinse the formamidinium tube using two additional 0.5-ml portions of hydriodic acid and add to the test tube containing the product, which at all times was kept in an inert atmosphere of flowing argon.\r\n\r\nMaintain the product in the hydriodic acid solution for 15 min at room temperature, with periodic agitation of the solution, and filter under flowing dry nitrogen gas.\r\n\r\nYield was approximately 75% of the theoretical yield. Dry black powder under vacuum at room temperature and store in an argon-filled glovebox, with oxygen and water levels maintained below 1 ppm.\",Single crystal X-ray diffraction,Enraf-Nonius CAD4 diffractometer with graphite-monochromatized MoKalpha (0.7107 angstrom) radiation. Refer to Page 377 X-ray diffraction section.\r\n10.1007/s12274-016-1051-8,Formamidinium tin bromide iodide,CH5N2SnI2Br,\"FASnI2Br, HC(NH2)2SnI2Br, diaminomethanide monobromo diiodostannate(II)\",CH5N2,\"SnI2Br, Tin bromide iodide\",diaminomethanide tin bromide iodide,3,film,,,,,,,,\"SnI2 (Sigma-Aldrich), FABr (Dyesol), N,N-dimethylformamide (anhydrous, Sigma-Aldrich), ITO/PEDOT:PSS substrate, chlorobenzene\",200 nm FASnI2Br film,\"373 mg of SnI2 and 125 mg of FABr in 1 ml N,N-dimethylformamide were mixed. This precursor solution was spin-coated at 2,500 rpm. 20 μL of chlorobenzene was dropped onto the spinning substrate 7 s after starting the spin-coating. The film was annealed at 75 °C for 5 min.\",UV-vis absorption,\"The absorption spectrum was recorded using V-650, Jasco spectrophotometer with an integrating sphere.\"\r\n10.1007/s12274-016-1401-6,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"HI, phenylethylamine, PbAc2•3H2O, IPA\",yellow crystals,\"First, PEAI was synthesized by adding HI (48 wt.% in water) to phenylethylamine at a molar ration of 1:1. This was performed at 0º C. Water was evaporated in a hood (at ~100º C) until PEAI crystals formed. Solution then cooled, powder product was filtered, washed with diethyl ether, and dried at 80º C in a vacuum oven for ~24 hours.\r\nNext, (PEA)2PbI4 was synthesized. Fluoride-doped  tin oxide (FTO) glass substrate was coated with a film of lead acetate by drop-casting PbAc2•3H2O (100 mg/mL). This was dried for 30 minutes at 60º C. The PbAc2 film was placed into PEAI solution in IPA, having various concentrations at room temperature. The lead-coated side was facing down in the vial. After the reaction (~20 hrs), the substrate was removed, dipped into IPA again to remove extra solution, and dried under a stream of N2.\",Single Crystal X-ray Diffraction,\"Single crystal was attached to tip of MiTeGen MicroMount, under a stream of N2 at 100 K. Data was recorded with Bruker Quazar SMART APEXII diffractometer with Mo Kα (λ = 0.71073 Å) radiation.\"\r\n10.1016/0022-3697(90)90021-7,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,single crystal,,,,,,,,\"Pb(CH3CO2)2, MACl\",Colorless MAPbCl3 cube-shaped crystals of 1-2 mm from the edge,Add aqueous solution of Pb(CH3CO2)2 drop by drop to an excess quantity of hot aqueous MACl solution and cool slowly to 5 °C.,Adiabatic calorimetry,\"The heat capacities were measured with a computerized adiabatic calorimeter [1, 2]. The temperature ranges of the measurement were between 13 and 300 K. The mass of the calorimetric sample was 6.0483 g.\"\r\n10.1016/0022-3697(90)90021-7,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,single crystal,,,,,,,,\"Pb(CH3CO2)2, MABr\",Orange MAPbBr3 cube-shaped crystals of 1-2 mm,Add aqueous solution of Pb(CH3CO2)2 drop by drop to an excess quantity of hot aqueous MABr solution and cool slowly to 5 °C.,Adiabatic calorimetry,\"The heat capacities were measured with a computerized adiabatic calorimeter [1, 2]. The temperature ranges of the measurement were between 13 and 300 K. The mass of the calorimetric sample was 8.8810 g.\"\r\n10.1016/0022-3697(90)90021-7,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"Pb(CH3CO2)2, MAI\",Black MAPbI3 cube-shaped crystals of 1-2 mm,\"Add aqueous solution of Pb(CH3CO2)2 drop by drop to an excess quantity of hot aqueous MAI solution and cool slowly, keeping temperature above 40 °C to prevent crystallization of (MA)3Pb6-2H2O.\",Adiabatic calorimetry,\"The heat capacities were measured with a computerized adiabatic calorimeter [1, 2]. The temperature ranges of the measurement were between 13 and 365 K. The mass of the calorimetric sample was 9.3384 g.\"\r\n10.1016/0038-1098(85)90959-7,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"HI, CH3NH2, Pb(NO3)2\",N-deuterated MAPbI3 crystals,Add concentrated HI to neutralize 20 g of 40% CH3NH2 aqueous solution (D2O-H2O mixture). Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH3I solution. Organic crystals form while dripping in the solution. Cool the solution to not below 40°C and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum.,2H and 14N NMR,\"2H and 14N NMR spectra were recorded at 55.4257 and 26.083 MHz, respectively, on a Nicolet 360 NB spectrometer (B0 = 8.48 T). Refer to Page 581.\"\r\n10.1016/0038-1098(85)90959-7,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,single crystal,,,,,,,,\"HBr, CH3NH2, Pb(NO3)2\",N-deuterated MAPbBr3 single crystals,Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution (D2O-H2O mixture). Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH3Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum.,2H and 14N NMR,\"2H and 14N NMR spectra were recorded at 55.4257 and 26.083 MHz, respectively, on a Nicolet 360 NB spectrometer (B0 = 8.48 T). Refer to Page 581.\"\r\n10.1016/0038-1098(85)90959-7,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,single crystal,,,,,,,,Not specified,MAPbCl3 single crystals,The procedure mentioned in ref [1] for MAPbBr3 was modified. A D2O-H2O mixture was used to prepare the N-deuterated samples.,2H and 14N NMR,\"2H and 14N NMR spectra were recorded at 55.4257 and 26.083 MHz, respectively, on a Nicolet 360 NB spectrometer (B0 = 8.48 T). Refer to Page 581.\"\r\n10.1016/j.chempr.2017.02.004,Bis(butylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16,\"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C4H12N, CH6N\",\"Pb5I16, Lead iodide\",bis(butane-1-aminium) tetrakis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, MACL, n-butylamine, HI, H3PO2\",Black crystals,\"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL,\r\n31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",Single-crystal X-ray diffraction,An image plate STOE IPDS II diffractometer with Mo Kα radiation (λ = 0.71073 Å) operated at 50 kV and 40 mA was used for SCXRD. The X-AREA suite was used for data reduction and absorption corrections. Charge flipping was used to solve the structure and refinement was performed by full-matrix least squares on F2 using the Jana2006 package.\r\n10.1016/j.chempr.2017.02.004,Bis(butylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16,\"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C4H12N, CH6N\",\"Pb5I16, Lead iodide\",bis(butane-1-aminium) tetrakis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, MACL, n-butylamine, HI, H3PO2\",Black crystals,\"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double beam, double-monochromator spectrophotometer was used to measure the optical diffuse reflectance spectra of powdered samples. BaSO4 was used as the 100% reflectance reference. The band gap was estimated after correcting for the excitonic peak and the Urbach tail in the absorption spectrum.\"\r\n10.1016/j.chempr.2017.02.004,Bis(butylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16,\"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C4H12N, CH6N\",\"Pb5I16, Lead iodide\",bis(butane-1-aminium) tetrakis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, MACL, n-butylamine, HI, H3PO2\",Black crystals,\"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double beam, double-monochromator spectrophotometer was used to measure the optical diffuse reflectance spectra of powdered samples. BaSO4 was used as the 100% reflectance reference. The band gap was estimated after correcting for the excitonic peak and the Urbach tail in the absorption spectrum.\"\r\n10.1016/j.chempr.2017.02.004,Bis(butylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16,\"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C4H12N, CH6N\",\"Pb5I16, Lead iodide\",bis(butane-1-aminium) tetrakis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, MACL, n-butylamine, HI, H3PO2\",Black crystals,\"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",Photoluminescence Spectra,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer was used to measure PL spectra on the crystals. A diode continuous wave laser, exciting at 473 nm, and a Synapse charge-coupled device camera was part of the instrument. The laser beam was parallel to the (010) direction of the crystals and was aimed at an area of 10 square microns on the surface.\"\r\n10.1016/j.chempr.2017.02.004,Bis(butylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16,\"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C4H12N, CH6N\",\"Pb5I16, Lead iodide\",bis(butane-1-aminium) tetrakis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, MACL, n-butylamine, HI, H3PO2\",Black crystals,\"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",Photoluminescence Spectra,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer was used to measure PL spectra on the crystals. A diode continuous wave laser, exciting at 473 nm, and a Synapse charge-coupled device camera was part of the instrument. The laser beam was parallel to the (010) direction of the crystals and was aimed at an area of 10 square microns on the surface.\"\r\n10.1016/j.jssc.2006.09.023,Histammonium lead bromide,C5H11N3PbBr4,\"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",C5H11N3,\"PbBr4, Lead bromide\",4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide,2,single crystal,,,,,,,,\"PbBr2 (99.99%), Histamine (98%), HBr (40%)\",Pink crystals (yield: 40.3%),\"Equimolar amounts of PbBr2 (0.367g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HBr by heating and refluxing at 90 °C and then, the solution slowly cooled to room temperature in N2 atmosphere.\",Single-crystal X-ray diffraction,A Rigaku RAXIS-RAPID image plate diffractometer employed the ω-scan technique and used Mo Kα radiation (λ=0.71069 Å). Structures were solved via direct methods using SHELXS-97 and full-matrix least-squares techniques using SHELXL-97 implemented in WINGX.\r\n10.1016/j.jssc.2006.09.023,Histammonium lead bromide,C5H11N3PbBr4,\"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",C5H11N3,\"PbBr4, Lead bromide\",4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide,2,film,,,,,,,,\"PbBr2 (99.99%), Histamine (98%), HBr (40%), DMF\",Thin film on quartz substrate,\"For preparing the crystals, equimolar amounts of PbBr2 (0.367g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HBr by heating and refluxing at 90 °C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 °C for 20 minutes.\",UV-Vis absorption,A Hitachi F-4100 spectrofluorimeter was used to record the UV-Vis absorption spectra.\r\n10.1016/j.jssc.2006.09.023,Histammonium lead bromide,C5H11N3PbBr4,\"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",C5H11N3,\"PbBr4, Lead bromide\",4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide,2,film,,,,,,,,\"PbBr2 (99.99%), Histamine (98%), HBr (40%), DMF\",Thin film on quartz substrate,\"For preparing the crystals, equimolar amounts of PbBr2 (0.367g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HBr by heating and refluxing at 90 °C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 °C for 20 minutes.\",Photoluminescence Spectroscopy,A Hitachi F-4500 spectrofluorimeter was used for emission spectra. A 150 W xenon lamp was used as the excitation source.\r\n10.1016/j.jssc.2006.09.023,Histammonium lead chloride,(C5H11N3)PbCl4,\"(HIS)PbCl4(HA)PbCl4, Histammonium lead chloride, 4-(2-ethanaminium)-1H-imidazol-3-ium tetrachloroplumbate\",C5H11N3,\"PbCl4, Lead chloride\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) chloride,2,film,,,,,,,,\"PbCl2 (99.99%), Histamine (98%), HCl (36%), DMF\",Thin film on quartz substrate,\"For preparing the crystals, equimolar amounts of PbCl2 (0.278g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HCl by heating and refluxing at 90 °C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 °C for 20 minutes.\",UV-Vis absorption,A Hitachi F-4100 spectrofluorimeter was used to measure the UV-Vis absorption spectra.\r\n10.1016/j.jssc.2006.09.023,Histammonium lead chloride,(C5H11N3)PbCl4,\"(HIS)PbCl4(HA)PbCl4, Histammonium lead chloride, 4-(2-ethanaminium)-1H-imidazol-3-ium tetrachloroplumbate\",C5H11N3,\"PbCl4, Lead chloride\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) chloride,2,film,,,,,,,,\"bCl2 (99.99%), Histamine (98%), HCl (36%), DMF\",Thin film on quartz substrate,\"For preparing the crystals, equimolar amounts of PbCl2 (0.278g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HCl by heating and refluxing at 90 °C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 °C for 20 minutes.\",Photoluminescence Spectroscopy,A Hitachi F-4500 spectrofluorimeter was used for emission spectra. A 150 W xenon lamp was used as the excitation source.\r\n10.1016/j.materresbull.2017.09.054,Methylammonium tin chloride,CH6NSnCl3,\"Methanaminium trichlorostannate(II), MASnCl3, CH3NH3SnCl3\",CH6N,\"SnCl3, Tin chloride\",methanaminium tin chloride,3,single crystal,,,,,,,,\"HCl, methylamine, SnCl2\",,\"Initially, methyl ammonium chloride (CH3NH3Cl) was synthesized by mixing 32.3 ml of HCl acid in 30 ml of methylamine. Powder of CH3NH3Cl was dissolved in the ethanol and was heated at 60 °C for four hours. The solution was frozen in the refrigerator for 3-5 days.  The obtained crystals were filtered.\r\n\r\nCH3NH3Cl powder (0.395 gm) and SnCl2 (1.157 gm) were mixed in 2 ml DMF and kept for stirring at 60 °C for 8 h.\",UV-vis absorption,\"A UV-vis spectrophotometer (Model no. UV-1800,SHIMADZU) was used to measure the UV-vis absorption.\"\r\n10.1016/j.nanoen.2016.09.009,Cesium tin bromide,CsSnBr3,Cesium tribromostannate(II),None,SnBr3,,3,film,,,,,,,,\"SnBr2 (Alfa Aesar 99.4%), SnF2 and CsBr\",yellow 97 nm thick CsSnBr3 film on glass,\"For the perovskite layer, the desired thicknesses of SnBr2, SnF2, and CsBr were vapor-deposited at a rate of ~0.5Ǻ/s under a base pressure of ~10−6 Torr.\",UV-vis absorption,\r\n10.1016/j.poly.2018.11.026,\"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO \",\"Pb4Cl10, Lead chloride\",\"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,single crystal,,,,,,,,\"S-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",Single Crystal X-ray Diffraction,A Bruker D8 ADVANCE Series II (MoKα radiation) was used to to collect data at room temperature. Structures were then solved and refined through the Shelxl and Olex software.\r\n10.1016/j.poly.2018.11.026,\"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO \",\"Pb4Cl10, Lead chloride\",\"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,powder,,,,,,,,\"S-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",infrared absorption,A Bruker VERTEX70 unit was used to collect data.\r\n10.1016/j.poly.2018.11.026,\"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO \",\"Pb4Cl10, Lead chloride\",\"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,single crystal,,,,,,,,\"S-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",UV-vis absorption,A Shimadzu UV-3600 spectrophotometer was used to collect measurements. Diffuse reflectance data were converted to optical absorption via the Kubelka-Munk equation.\r\n10.1016/j.poly.2018.11.026,\"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO \",\"Pb4Cl10, Lead chloride\",\"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,single crystal,,,,,,,,\"S-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",Photoluminescence,\"A Horiba Jobi-Yvon LabRAM ARAMIS system was used to collect data at room temperature. The sample was excited with a 325nm He-Cd laser, focused through a 40x UV objective.\"\r\n10.1016/j.poly.2018.11.026,\"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO \",\"Pb4Cl10, Lead chloride\",\"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,powder,,,,,,,,\"S-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",Thermogravimetric Analysis,A NETZSCH-STA-449F3 was used to collect data when the sample was in a dry nitrogen atmosphere.\r\n10.1016/j.poly.2018.11.026,\"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO\",\"Pb4Cl10, Lead chloride\",\"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,single crystal,,,,,,,,\"R-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",Single Crystal X-ray Diffraction,A Bruker D8 ADVANCE Series II (MoKα radiation) was used to to collect data at room temperature. Structures were then solved and refined through the Shelxl and Olex software.\r\n10.1016/j.poly.2018.11.026,\"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO\",\"Pb4Cl10, Lead chloride\",\"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,single crystal,,,,,,,,\"R-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",UV-vis absorption,A Shimadzu UV-3600 spectrophotometer was used to collect measurements. Diffuse reflectance data were converted to optical absorption via the Kubelka-Munk equation.\r\n10.1016/j.poly.2018.11.026,\"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO\",\"Pb4Cl10, Lead chloride\",\"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,single crystal,,,,,,,,\"R-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",Photoluminescence,\"A Horiba Jobi-Yvon LabRAM ARAMIS system was used to collect data at room temperature. The sample was excited with a 325nm He-Cd laser, focused through a 40x UV objective.\"\r\n10.1016/j.poly.2018.11.026,\"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO\",\"Pb4Cl10, Lead chloride\",\"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,powder,,,,,,,,\"R-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",infrared absorption,A Bruker VERTEX70 unit was used to collect data.\r\n10.1016/j.poly.2018.11.026,\"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",C30H42Cl10O2Pb4,\"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] ‚Ä¢ 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\"C12H14N, C3H7NO\",\"Pb4Cl10, Lead chloride\",\"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",2,powder,,,,,,,,\"R-NEA, PbCl2, DMF, 2-butanol\",clear crystals,\"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",Thermogravimetric Analysis,A NETZSCH-STA-449F3 was used to collect data when the sample was in a dry nitrogen atmosphere.\r\n10.1016/j.synthmet.2015.11.028,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,single crystal,,,,,,,,\"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",Red crystals,MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.,Single-crystal X-ray diffraction,A Rapid Auto diffractometer was used at 293 K to collect SCXRD data using Mo Kα radiation (= 0.71073 Å). The structure was solved and refined with the SHELXL-software programs.\r\n10.1016/j.synthmet.2015.11.028,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,powder,,,,,,,,\"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",Red crystals,MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.,IR Spectroscopy,A Themo NICOLET-380 spectrophotometer was used to measure the IR spectra over the range 4000-400 cm^(-1). The samples were prepared with the KBr pellet method.\r\n10.1016/j.synthmet.2015.11.028,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,film,,,,,,,,\"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",Red film,MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.,UV-vis absorption spectroscopy,A Shimadzu UV-1800 spectrophotometer was used to measure the UV-vis absorption spectra over the range 200-800 nm at room temperature.\r\n10.1016/j.synthmet.2015.11.028,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,film,,,,,,,,\"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",Red film,MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.,Photoluminescence Spectroscopy,A Horiba Flurolog 3 was used to measure the PL emission spectra of the samples by exciting at 560 nm at room temperature.\r\n10.1016/j.synthmet.2015.11.028,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,film,,,,,,,,\"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",Red film,MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.,Photoluminescence Spectroscopy,A Horiba Flurolog 3 was used to measure the PL emission spectra of the samples by exciting at 560 nm at room temperature.\r\n10.1021/acs.chemmater.0c01254.s001,Bis(phenethylammonium) tin bromide,(C6H5CH2CH2NH3)2SnBr4,\"(PEA)2SnBr4, bis(phenethylaminium) tetrabromostannate(II)\",C6H5CH2CH2NH3,\"SnBr4, Tin bromide\",bis(phenethylaminium) tin bromide,2,single crystal,,,,,,,,\"SnBr2, C6H5CH2CH2NH3Br, HBr, H3PO2\",yellow flake single crystals,Growing the single crystal through the slow cooling process from 100 °C to room temperature. 2.0 mmol of SnBr2 and 4.0 mmol of PEABr are dissolved in a mixture of HBr (3 mL) and H3PO2 (1 mL) after magnetic stirring and nitrogen flow for ∼5 min at 100 °C. The solution is slowly cooled from 100 °C to room temperature. The obtained yellow flake single crystals are washed using acetone and ethyl ether and then dried under reduced pressure.,single-crystal X-ray diffraction,A Rigaku XtaLAB Synergy-S diffractometer using a HyPix-6000HE Hybrid Photon Counting (HPC) detector and a dual Mo and Cu microfocus sealed X-ray source as well as a low-temperature Oxford Cryosystem 800 is utilized to collect single-crystal X-ray data.\r\n10.1021/acs.chemmater.1c03492,Bis(3-iodopropylammonium) lead iodide,C6H18N2PbI6,\"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",C3H9NI,\"PbI4, Lead iodide\",bis(3-iodopropylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI (57% (w/w) in water), H3PO2 (50% (w/w) in water)\",yellow plate-like crystals,\"5 mmol PbO was dissolved in a solution of 40 mL HI and 5 mL of H3PO2 by sonicating in an ultrasonic bath sonicator for 10 min. The solution is cooled to ∼278 K using an ice−water bath. In this solution, 10 mmol H2N-(CH2)3-OH is added dropwise. The solution is stirred using a magnetic stirrer and heated for 30 min in an oil bath maintained at 383 K.  After 30 min, the heating and stirring are stopped, and the solution is kept undisturbed. After 12 hours, the precipitated crystals are separated by filtration with diethyl ether and dried in air.\",Diffuse reflectance spectroscopy,The spectrum was recorded using a Shimadzu UV3600 plus UV−vis−NIR spectrophotometer with BaSO4 powder as a reference of 100% reflectance. The reflectance signal is converted to absorbance using the Kubelka−Munk function.\r\n10.1021/acs.chemmater.1c03492,Ruddlesden-Popper,(RNH3)2(A)n−1MX3n+1,*,N/A,(A)n−1MX3n+1,,2,single crystal,,,,,,,,\"PbO, HI (57% (w/w) in water), H3PO2 (50% (w/w) in water)\",yellow plate-like crystals,\"5 mmol PbO was dissolved in a solution of 40 mL HI and 5 mL of H3PO2 by sonicating in an ultrasonic bath sonicator for 10 min. The solution is cooled to ∼278 K using an ice−water bath. In this solution, 10 mmol H2N-(CH2)3-OH is added dropwise. The solution is stirred using a magnetic stirrer and heated for 30 min in an oil bath maintained at 383 K.  After 30 min, the heating and stirring are stopped, and the solution is kept undisturbed. After 12 hours, the precipitated crystals are separated by filtration with diethyl ether and dried in air.\",Diffuse reflectance spectroscopy,The spectrum was recorded using a Shimadzu UV3600 plus UV−vis−NIR spectrophotometer with BaSO4 powder as a reference of 100% reflectance. The reflectance signal is converted to absorbance using the Kubelka−Munk function.\r\n10.1021/acs.chemmater.1c04213,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"phenethylammonium iodide (C8H12IN), lead iodide (PbI2)\",thin film,\"(PEA)I, amd PbI2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196°C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 μm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm × 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 °C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 × 10–5 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110°.\",UV-vis absorption,UV−vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\r\n10.1021/acs.chemmater.1c04213,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"phenethylammonium iodide (C8H12IN), lead iodide (PbI2)\",thin film,\"(PEA)I, amd PbI2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196°C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 μm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm × 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 °C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 × 10–5 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110°.\",UV-vis photoluminescence,PL spectroscopy measurements were taken using a HORIBA Jobin Yvon LabRam ARAMIS system. All films were excited using a 325 HeCd laser source with a 1% filter. Samples were kept in ambient air conditions.\r\n10.1021/acs.chemmater.1c04213,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,film,,,,,,,,\"phenethylammonium bromide (C8H12BrN), lead bromide (PbBr2)\",Thin film of (C12H25NH3)2PbBr4,\"(PEA)Br and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196°C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 μm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm × 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 °C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 × 10–5 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110°.\",UV-Vis absorption,UV−vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\r\n10.1021/acs.chemmater.1c04213,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,film,,,,,,,,\"phenethylammonium bromide (C8H12BrN), lead bromide (PbBr2)\",Thin film of (C12H25NH3)2PbBr4,\"(PEA)Br and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196°C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 μm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm × 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 °C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 × 10–5 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110°.\",UV-Vis absorption,PL spectroscopy measurements were taken using a HORIBA Jobin Yvon LabRam ARAMIS system. All films were excited using a 325 HeCd laser source with a 1% filter. Samples were kept in ambient air conditions.\r\n10.1021/acs.chemmater.1c04213,Bis(phenethylammonium) lead iodide(1-x) bromide(x): x = 0.25,PEA2Pb(I(1-x)Br(x))4 with x = 0.25,\"PEA2 lead iodide bromide, PEAPbIBr, PEA2PbIBr\",C8NH12,Pb(I(1-x)Br(x))4,bis(phenethylaminium) lead (II) iodide bromide,2,film,,,,,,,,\"phenethylammonium iodide (C8H12IN), phenethylammonium bromide (C8H12BrN), lead iodide (PbI2), lead bromide (PbBr2)\",thin film,\"(PEA)I, (PEA)Br, PbI2, and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196°C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 μm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm × 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 °C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 × 10–5 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110°.\",UV−vis Absorption,UV−vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\r\n10.1021/acs.chemmater.1c04213,Bis(phenethylammonium) lead iodide(1-x) bromide(x): x = 0.5,PEA2Pb(I(1-x)Br(x))4 with x = 0.5,\"PEA2 lead iodide bromide, PEAPbIBr, PEA2PbIBr\",C8NH12,Pb(I0.5Br0.5)4,bis(phenethylaminium) lead (II) iodide bromide,2,film,,,,,,,,\"phenethylammonium iodide (C8H12IN), phenethylammonium bromide (C8H12BrN), lead iodide (PbI2), lead bromide (PbBr2)\",thin film,\"(PEA)I, (PEA)Br, PbI2, and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196°C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 μm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm × 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 °C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 × 10–5 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110°.\",UV−vis absorption,UV−vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\r\n10.1021/acs.chemmater.1c04213,Bis(phenethylammonium) lead iodide(1-x) bromide(x): x = 0.75,PEA2Pb(I(1-x)Br(x))4 with x = 0.75,\"PEA2 lead iodide bromide, PEAPbIBr, PEA2PbIBr\",C8NH12,Pb(I0.25Br0.75)4,bis(phenethylaminium) lead (II) iodide bromide,2,film,,,,,,,,\"phenethylammonium iodide (C8H12IN), phenethylammonium bromide (C8H12BrN), lead iodide (PbI2), lead bromide (PbBr2)\",thin film,\"(PEA)I, (PEA)Br, PbI2, and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196°C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 μm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm × 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 °C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 × 10–5 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110°.\",UV−vis absorption,UV−vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\r\n10.1021/acs.chemmater.5b04231,Cesium silver bismuth chloride,Cs2AgBiCl6,Dicesium trichloroargentate(I) µ-dichloro trichlorobismuthate(III),None,\"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",,3,bulk polycrystalline,,,,,,,,\"Cs2CO3 (99+%, Strem Chemicals), HCl (Sigma-Aldrich, 37%), AgNO3 (99.9+%, Alfa Aesar), NaCl (ACS Reagent, GFS Chemicals), BiCl3 (≥98%, Aldrich)\",Polycrystalline Cs2AgBiCl6,\"Cs2CO3 was reacted with HCl to prepare CsCl. The solution was evaporated, and the resulting solids were filtered and washed with ethanol. AgCl was precipitated by mixing aqueous solutions of AgNO3 and NaCl. \r\nThen, 8 mL of 12.1 M HCl and 2 mL of a 50% solution of H3PO2 were mixed and heated to 120 °C. To it, 1.89 mmol of AgCl and an equal amount of BiCl3 were added. When dissolved, 3.78 mmol of CsCl was added. The precipitate was collected [possibly after cooling down the solution to room temperature] on filter paper, washed with ethanol, and dried overnight.\",X-ray Powder Diffraction,\"Powder XRD data were collected on a Bruker D8 powder diffractometer (40 kV, 50 mA, sealed Cu X-ray tube) equipped with an incident beam Ge 111 monochromator and Lynx Eye position-sensitive detector.\"\r\n10.1021/acs.chemmater.5b04231,Cesium silver bismuth bromide,Cs2AgBiBr6,Dicesium tribromoargentate(I) tribromobismuthate(III),None,AgBiBr6,,3,bulk polycrystalline,,,,,,,,\"Cs2CO3 (99+%, Strem Chemicals), HBr (Fluka, ≥48%), AgNO3 (99.9+%, Alfa Aesar), KBr (99+%, Alfa Aesar), Bi2O3 (≥99.0%, J.T. Baker)\",Polycrystalline Cs2AgBiCl6,\"Cs2CO3 was reacted with HBr to prepare CsBr. The solution was evaporated, and the resulting solids were filtered and washed with ethanol. AgBr was precipitated by mixing aqueous solutions of AgNO3 and KBr. BiBr3 was prepared by reacting Bi2O3 with HBr. The mixture was heated until fully dissolved, evaporated to dryness, and then filtered and washed with ethanol. \r\nThen, 8 mL of 8.84 M HBr and 2 mL of a 50% solution of H3PO2 were mixed and heated to 120 °C. To it, 1.41 mmol of AgBr and an equal amount of BiBr3 were added. When dissolved, 2.82 mmol of CsBr was added. The precipitate was collected [possibly after cooling down the solution to room temperature] on filter paper, washed with ethanol, and dried overnight.\",X-ray Powder Diffraction,\"Powder XRD data were collected on a Bruker D8 powder diffractometer (40 kV, 50 mA, sealed Cu X-ray tube) equipped with an incident beam Ge 111 monochromator and Lynx Eye position-sensitive detector.\"\r\n10.1021/acs.chemmater.6b00847,Bis(1-butylammonium) tris(methylammonium) lead iodide,C11H39N5Pb4I13,\"(BA)2(MA)3Pb4I13, bis(butane-1-aminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C4H12N, CH6N\",\"PbI4, Lead iodide\",bis(butane-1-aminium) tris(methanaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",Black plate-like (BA)2(MA)3Pb4I13 crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of HI solution (10.0 mL, 76 mmol) and  H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. \r\nSubsequent addition of solid CH3NH3Cl (507 mg, 7.5 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (248 μL, 2.5 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution.\r\nAddition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time black rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after ∼2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",Single Crystal X-ray diffraction,\"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\"\r\n10.1021/acs.chemmater.6b00847,Bis(1-butylammonium) bis(methylammonium) lead iodide,C10H36N4Pb3I10,\"bis(butane-1-aminium) di(methanaminium) decaiodo triplumbate(II), (BA)2(MA)2Pb3I10\",\"C4H12N, CH6N\",\"Pb3I10, Lead iodide\",bis(butane-1-aminium) di(methanaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",Dark red plate-like (BA)2(MA)2Pb3I10 crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of HI solution (10.0 mL, 76 mmol) and H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (450 mg, 6.67 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (327 μL, 3.33 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which was subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time deep-red/purple rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after ∼2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",Single Crystal X-ray diffraction,\"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\"\r\n10.1021/acs.chemmater.6b00847,Bis(1-butylammonium) bis(methylammonium) lead iodide,C10H36N4Pb3I10,\"bis(butane-1-aminium) di(methanaminium) decaiodo triplumbate(II), (BA)2(MA)2Pb3I10\",\"C4H12N, CH6N\",\"Pb3I10, Lead iodide\",bis(butane-1-aminium) di(methanaminium) lead (II) iodide,2,single crystal,VASP,DFT,PBEsol,,,,fully relaxed the internal atomic positions until the forces were less than 1 meV Å−1 using a 500 eV plane-wave cutoff,\"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",,\"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (450 mg, 6.67 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (327 μL, 3.33 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which was subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time deep-red/purple rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after ∼2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",Single Crystal X-ray diffraction,\"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\"\r\n10.1021/acs.chemmater.6b00847,Bis(1-butylammonium) tris(methylammonium) lead iodide,C11H39N5Pb4I13,\"(BA)2(MA)3Pb4I13, bis(butane-1-aminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C4H12N, CH6N\",\"PbI4, Lead iodide\",bis(butane-1-aminium) tris(methanaminium) lead (II) iodide,2,single crystal,VASP,DFT,PBEsol,,,,fully relaxed the internal atomic positions until the forces were less than 1 meV Å−1 using a 500 eV plane-wave cutoff,\"Lead Oxide (PbO), aqueous HI, aqueous H3PO2, n-CH3(CH2)3NH3I , solid CH3NH3Cl\",,\"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (507 mg, 7.5 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (248 μL, 2.5 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time black rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after ∼2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",Single Crystal X-ray diffraction,\"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\"\r\n10.1021/acs.chemmater.6b00847,Bis(1-butylammonium) tris(methylammonium) lead iodide,C11H39N5Pb4I13,\"(BA)2(MA)3Pb4I13, bis(butane-1-aminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C4H12N, CH6N\",\"PbI4, Lead iodide\",bis(butane-1-aminium) tris(methanaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Lead Oxide (PbO), aqueous HI, aqueous H3PO2, n-CH3(CH2)3NH3I , solid CH3NH3Cl\",Black plate-like (BA)2(MA)3Pb4I13 crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (507 mg, 7.5 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (248 μL, 2.5 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time black rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after ∼2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",Photoluminescence spectroscopy,\"Oriented rectangular crystals were used in the collection of photoluminescence spectra. Crystals of type (BA)2(MA)3Pb4I13 provided data for the material with n=4. A Horiba LabRam Evolution Raman microscope spectrometer with a diode CW laser (600 g/mm diffraction grating; 473 m, 25 mW) and a Synapse CCD camera carried out measurements. The laser beam was focused at about 1 µm spot size was made parallel to the 010 orientation of the crystals. The power output of the laser source was limited to 0.1% of the maximum power output.\"\r\n10.1021/acs.chemmater.6b00847,Bis(1-butylammonium) bis(methylammonium) lead iodide,C10H36N4Pb3I10,\"bis(butane-1-aminium) di(methanaminium) decaiodo triplumbate(II), (BA)2(MA)2Pb3I10\",\"C4H12N, CH6N\",\"Pb3I10, Lead iodide\",bis(butane-1-aminium) di(methanaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",Dark red plate-like (BA)2(MA)2Pb3I10 crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of HI solution (10.0 mL, 76 mmol) and H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (450 mg, 6.67 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (327 μL, 3.33 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which was subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time deep-red/purple rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after ∼2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",Photoluminescence spectroscopy,\"Oriented rectangular crystals were used in the collection of photoluminescence spectra. Crystals of type (BA)2(MA)2Pb3I10 provided data for the material with n=3. A Horiba LabRam Evolution Raman microscope spectrometer with a diode CW laser (600 g/mm diffraction grating; 473 m, 25 mW) and a Synapse CCD camera carried out measurements. The laser beam was focused at about 1 µm spot size was made parallel to the 010 orientation of the crystals. The power output of the laser source was limited to 0.1% of the maximum power output.\"\r\n10.1021/acs.chemmater.6b02208,Bis(hexylammonium) copper chloride,(C6H13NH3)2CuCl4,\"C6MnCl, bis(hexylaminium) tetrachloromanganate(II)\",C6NH16,\"CuCl4, Copper chloride\",bis(hexylaminium) copper chloride,0,single crystal,,,,,,,,\"hydrochloric acid (37%), hexylamine, ethanol, diethyl ether, CuCl2.2H2O\",Yellow plate-like crystals,\"Hexylammonium chloride was synthesized by reacting HCl (5.85 mL, 70.00 mmol) with a cold stirred solution of hexylamine (9.34 mL, 70.00 mmol) 10 mL in ethanol. The solvent was evaporated using a rotary evaporator at 60 degrees C, and the obtained solid was washed with diethyl ether and dried overnight.\r\n3.90 mmol of hexylammonium chloride and 1.95 mmol of CuCl2 were dissolved in 2.5 mL of water by heating. The solution was slowly cooled to room temperature.\",Single crystal X-ray diffraction,Frames were collected using a Bruker DUO diffractometer using Mo Kα radiation (λ = 0.710 73 Å) and an APEXII CCD area detector\r\n10.1021/acs.chemmater.6b03054,Histammonium lead iodide,(C5H11N3)PbI4,\"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",C5H11N3,\"PbI4, Lead iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, histamine dihydrochloride\",Dark orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Single-crystal X-ray diffraction,Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\r\n10.1021/acs.chemmater.6b03054,Histammonium lead iodide,(C5H11N3)PbI4,\"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",C5H11N3,\"PbI4, Lead iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, histamine dihydrochloride\",Dark orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Time-Resolved Photoluminescence Spectroscopy,TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\r\n10.1021/acs.chemmater.6b03054,Histammonium lead iodide,(C5H11N3)PbI4,\"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",C5H11N3,\"PbI4, Lead iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, histamine dihydrochloride\",Dark orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.6b03054,Histammonium lead iodide,(C5H11N3)PbI4,\"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",C5H11N3,\"PbI4, Lead iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, histamine dihydrochloride\",Dark orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.6b03054,Histammonium tin iodide,(C5H11N3)SnI4,\"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",C5H11N3,\"SnI4, Tin iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, histamine dihydrochloride\",Black plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Single-crystal X-ray diffraction,Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\r\n10.1021/acs.chemmater.6b03054,Histammonium tin iodide,(C5H11N3)SnI4,\"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",C5H11N3,\"SnI4, Tin iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, histamine dihydrochloride\",Black plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Time-Resolved Photoluminescence Spectroscopy,TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\r\n10.1021/acs.chemmater.6b03054,Histammonium tin iodide,(C5H11N3)SnI4,\"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",C5H11N3,\"SnI4, Tin iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, histamine dihydrochloride\",Black plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.6b03054,Histammonium tin iodide,(C5H11N3)SnI4,\"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",C5H11N3,\"SnI4, Tin iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, histamine dihydrochloride\",Black plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) lead iodide,C14H20N2PbI4,\"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",C7H10N,\"PbI4, lead iodide\",bis(benzylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, benzylamine hydrochloride\",Orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Single-crystal X-ray diffraction,Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) lead iodide,C14H20N2PbI4,\"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",C7H10N,\"PbI4, lead iodide\",bis(benzylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, benzylamine hydrochloride\",Orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Time-Resolved Photoluminescence Spectroscopy,TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) lead iodide,C14H20N2PbI4,\"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",C7H10N,\"PbI4, lead iodide\",bis(benzylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, benzylamine hydrochloride\",Orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) lead iodide,C14H20N2PbI4,\"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",C7H10N,\"PbI4, lead iodide\",bis(benzylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, benzylamine hydrochloride\",Orange plate-like crystals,PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) tin iodide,(C7NH10)2SnI4,\"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",C7H10N,\"SnI4, Tin iodide\",bis(benzylaminium) tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, benzylamine hydrochloride\",Dark red plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Single-crystal X-ray diffraction,Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) tin iodide,(C7NH10)2SnI4,\"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",C7H10N,\"SnI4, Tin iodide\",bis(benzylaminium) tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, benzylamine hydrochloride\",Dark red plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Time-Resolved Photoluminescence Spectroscopy,TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) tin iodide,(C7NH10)2SnI4,\"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",C7H10N,\"SnI4, Tin iodide\",bis(benzylaminium) tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, benzylamine hydrochloride\",Dark red plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.6b03054,Bis(benzylammonium) tin iodide,(C7NH10)2SnI4,\"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",C7H10N,\"SnI4, Tin iodide\",bis(benzylaminium) tin iodide,2,single crystal,,,,,,,,\"SnCl2·2H2O, HI, H3PO2, benzylamine hydrochloride\",Dark red plate-like crystals,SnCl2·2H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.,Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\"\r\n10.1021/acs.chemmater.8b03436,bis(2-phenethylammonium) methylammonium lead iodide,C17H30N3Pb2I7,\"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\"C8H12N, CH6N\",\"Pb2I7, Lead iodide\",bis(2-phenylethanaminium) methanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Hydroiodic acid, Lead oxide, Methylammonium Iodide, Phenylethylammonium\",,\"single crystals were grown using a previously reported cooling method. Briefly, precursors containing lead oxide, methylammonium iodide, and phenethylamine with specific ratios were dissolved in hydriodic. acid (HI) solution (57% w/w in water) at ∼90 °C. The solution was then slowly cooled to room temperature at a rate of 1 °C/h. The ratios are 1.72/0/3.45 mmol, 6/18/1 mmol, and 10/24/1 mmol for n = 1, 2, 3, respectively, in 30 mL of HI solution. It is worth noting that larger n-members (n > 3) of this 2D perovskite family can be also grown but in a mixture form, which should be caused by a large solubility difference between PEA and MA in the aqueous solution. MAPbI3 and MAPbBr3 single crystals were grown as previously reported.46 As-grown crystals were rinsed with diethyl ether and then dried under vacuum.\",Single crystal XRD,\"XRD was carried out with a Bruker D8\r\nAdvance using a Cu Kα1 (λ = 1.5406 Å) source, a step size of\r\n0.02°, and a speed of 0.5 s/step. The absorption spectra were\r\ncaptured by measuring the diffuse reflectance spectra of crystal\r\npowders using a Cary 5000 (Agilent Technologies).\"\r\n10.1021/acs.chemmater.8b03436,bis(2-phenethylammonium) methylammonium lead iodide,C17H30N3Pb2I7,\"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\"C8H12N, CH6N\",\"Pb2I7, Lead iodide\",bis(2-phenylethanaminium) methanaminium lead (II) iodide,2,single crystal,Quantum ESPRESSO,DFT,PBE,,Including scaler relativistic,,Single-particle wave functions (charges) were expanded on a plane-wave basis set up to a kinetic energy cutoff of 50 Ry (300 Ry). The crystal structures were fully relaxed until the total force on each atom was less than 0.01 eV/Å,\"Hydroiodic acid, Lead oxide, Methylammonium Iodide, Phenylethylammonium\",,\"single crystals were grown using a previously reported cooling method. Briefly, precursors containing lead oxide, methylammonium iodide, and phenethylamine with specific ratios were dissolved in hydriodic. acid (HI) solution (57% w/w in water) at ∼90 °C. The solution was then slowly cooled to room temperature at a rate of 1 °C/h. The ratios are 1.72/0/3.45 mmol, 6/18/1 mmol, and 10/24/1 mmol for n = 1, 2, 3, respectively, in 30 mL of HI solution. It is worth noting that larger n-members (n > 3) of this 2D perovskite family can be also grown but in a mixture form, which should be caused by a large solubility difference between PEA and MA in the aqueous solution. MAPbI3 and MAPbBr3 single crystals were grown as previously reported.46 As-grown crystals were rinsed with diethyl ether and then dried under vacuum.\",Single crystal XRD,\"XRD was carried out with a Bruker D8\r\nAdvance using a Cu Kα1 (λ = 1.5406 Å) source, a step size of\r\n0.02°, and a speed of 0.5 s/step. The absorption spectra were\r\ncaptured by measuring the diffuse reflectance spectra of crystal\r\npowders using a Cary 5000 (Agilent Technologies).\"\r\n10.1021/acs.chemmater.8b03436,bis(2-phenethylammonium) methylammonium lead iodide,C17H30N3Pb2I7,\"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\"C8H12N, CH6N\",\"Pb2I7, Lead iodide\",bis(2-phenylethanaminium) methanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",Red (PEA)2MAPb2I7 crystals,\"6 mmol PbO, 18 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 °C. The vial was then kept in an oven at 110 °C for 4 h. The solution was then slowly cooled to room temperature.\",Photoluminescence,\"For steady-state PL measurements, the details are not available in the paper.\"\r\n10.1021/acs.chemmater.8b03436,bis(phenylethylammonium) bis(methylammonium) lead iodide,C18H36N4Pb3I10,\"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\"C8H12N, CH6N\",\"Pb3I10, Lead iodide\",bis(2-phenylethanaminium) bismethanaminium lead (II) iodide,2,single crystal,Quantum ESPRESSO,DFT,PBE,,Including scaler relativistic,,Single-particle wave functions (charges) were expanded on a plane-wave basis set up to a kinetic energy cutoff of 50 Ry (300 Ry). The crystal structures were fully relaxed until the total force on each atom was less than 0.01 eV/Å,\"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",Black (PEA)2MA2Pb3I10 crystals,\"10 mmol PbO, 24 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 °C. The vial was then kept in an oven at 110 °C for 4 h. The solution was then slowly cooled to room temperature.\",Single crystal XRD,\"XRD was carried out with a Bruker D8\r\nAdvance using a Cu Kα1 (λ = 1.5406 Å) source, a step size of\r\n0.02°, and a speed of 0.5 s/step. The absorption spectra were\r\ncaptured by measuring the diffuse reflectance spectra of crystal\r\npowders using a Cary 5000 (Agilent Technologies).\"\r\n10.1021/acs.chemmater.8b03436,bis(phenylethylammonium) bis(methylammonium) lead iodide,C18H36N4Pb3I10,\"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\"C8H12N, CH6N\",\"Pb3I10, Lead iodide\",bis(2-phenylethanaminium) bismethanaminium lead (II) iodide,2,single crystal,Quantum ESPRESSO,DFT,PBE,,Including scaler relativistic,,Single-particle wave functions (charges) were expanded on a plane-wave basis set up to a kinetic energy cutoff of 50 Ry (300 Ry). The crystal structures were fully relaxed until the total force on each atom was less than 0.01 eV/Å,\"Hydroiodic acid, Lead oxide, Methylammonium Iodide, Phenylethylammonium\",,\"single crystals were grown using a previously reported cooling method. Briefly, precursors containing lead oxide, methylammonium iodide, and phenethylamine with specific ratios were dissolved in hydriodic. acid (HI) solution (57% w/w in water) at ∼90 °C. The solution was then slowly cooled to room temperature at a rate of 1 °C/h. The ratios are 1.72/0/3.45 mmol, 6/18/1 mmol, and 10/24/1 mmol for n = 1, 2, 3, respectively, in 30 mL of HI solution. It is worth noting that larger n-members (n > 3) of this 2D perovskite family can be also grown but in a mixture form, which should be caused by a large solubility difference between PEA and MA in the aqueous solution. MAPbI3 and MAPbBr3 single crystals were grown as previously reported.46 As-grown crystals were rinsed with diethyl ether and then dried under vacuum.\",Single crystal XRD,\"XRD was carried out with a Bruker D8\r\nAdvance using a Cu Kα1 (λ = 1.5406 Å) source, a step size of\r\n0.02°, and a speed of 0.5 s/step. The absorption spectra were\r\ncaptured by measuring the diffuse reflectance spectra of crystal\r\npowders using a Cary 5000 (Agilent Technologies).\"\r\n10.1021/acs.chemmater.8b03436,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,VESTA,DFT,PBE+SOC+vdW,6x6x1,,PAW,Plane-wave cutoff energy: 500 eV,,,,,\r\n10.1021/acs.chemmater.8b03436,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"hydriodic acid (57% w/w in water, Alpha Aesar), phenethylamine (PEA),  lead oxide (PbO, 99%, Sigma-Aldrich)\",Orange (PEA)2PbI4 crystals,\"In 30 mL HI solution, PEA, and PbO (ratio: 1.72: 3.45 mmol) were dissolved. The solution was heated at 110º C for 4 hours and subsequently cooled to room temperature. Once the solution cooled, single crystals formed.\",Single crystal X-ray diffraction,\r\n10.1021/acs.chemmater.8b03436,bis(2-phenethylammonium) methylammonium lead iodide,C17H30N3Pb2I7,\"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\"C8H12N, CH6N\",\"Pb2I7, Lead iodide\",bis(2-phenylethanaminium) methanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",Red (PEA)2MAPb2I7 crystals,\"6 mmol PbO, 18 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 °C. The vial was then kept in an oven at 110 °C for 4 h. The solution was then slowly cooled to room temperature.\",Photoluminescence,\"For steady-state PL measurements, the details are not available in the paper.\"\r\n10.1021/acs.chemmater.8b03436,bis(phenylethylammonium) bis(methylammonium) lead iodide,C18H36N4Pb3I10,\"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\"C8H12N, CH6N\",\"Pb3I10, Lead iodide\",bis(2-phenylethanaminium) bismethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",Black (PEA)2MA2Pb3I10 crystals,\"10 mmol PbO, 24 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 °C. The vial was then kept in an oven at 110 °C for 4 h. The solution was then slowly cooled to room temperature.\",Photoluminescence,\"For steady-state PL measurements, the details are not available in the paper.\"\r\n10.1021/acs.chemmater.8b03436,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"hydriodic acid (57% w/w in water, Alpha Aesar), phenethylamine (PEA),  lead oxide (PbO, 99%, Sigma-Aldrich)\",Orange (PEA)2PbI4 crystals,\"In 30 mL HI solution, PEA, and PbO (ratio: 1.72: 3.45 mmol) were dissolved. The solution was heated at 110º C for 4 hours and subsequently cooled to room temperature. Once the solution cooled, single crystals formed.\",Single crystal X-ray diffraction,\r\n10.1021/acs.chemmater.8b03436,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,VESTA,DFT,PBE+SOC+vdW,6x6x1,,PAW,Plane-wave cutoff energy: 500 eV,,,,,\r\n10.1021/acs.chemmater.8b04064,Pyridiniumethylammonium lead iodide,C7H14I4N2Pb,(PyrEA)[PbI4],C7H14N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-pyridin-1-ium,2,single crystal,,,,,,,,\"pyridine, iodoethylammonium iodide, anhydrous acetonitrile, PbI2, HI\",red plate crystals,\"First, PyrEAI was synthesized by charging a flamed-dried two-neck round bottom flask with pyridine (1.05 equivalent), iodoethylammonium iodide (1.00 equivalent), and anhydrous acetonitrile (which was dried with CaH2 before distillation). The mixture was heated and stirred at reflux for 2 days. The mixture was then cooled to room temperature. The precipitate was isolated by filtration, washed with diethyl ether, and dried. \r\nThen, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and PyrEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140ºC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",Single Crystal X-ray Diffraction,\"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo Kα radiation (0.71073Å) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\"\r\n10.1021/acs.chemmater.8b04064,Pyridiniumethylammonium lead iodide,C7H14I4N2Pb,(PyrEA)[PbI4],C7H14N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-pyridin-1-ium,2,film,,,,,,,,,,,,Wavelength used was λ = 0.71073 Å.\r\n10.1021/acs.chemmater.8b04064,Pyridiniumethylammonium lead iodide,C7H14I4N2Pb,(PyrEA)[PbI4],C7H14N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-pyridin-1-ium,2,film,,,,,,,,,,,UV-vis absorption,Band gap data was obtained by linear-fitting the UV-vis absorption spectra.\r\n10.1021/acs.chemmater.8b04064,Pyridiniumethylammonium lead iodide,C7H14I4N2Pb,(PyrEA)[PbI4],C7H14N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-pyridin-1-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PyrEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,UV-Vis absorption,Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\r\n10.1021/acs.chemmater.8b04064,Pyridiniumethylammonium lead iodide,C7H14I4N2Pb,(PyrEA)[PbI4],C7H14N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-pyridin-1-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PyrEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,UV-Vis spectroscopy and scanning electron microscopy,\"UV-vis absorption spectra were recorded using a SHIMADZU UV-3600 spectrophotometer, with an integrating sphere (ISR-3100) in the wavelength range 300-800nm. Film thickness was calculated by cross-section images of the thin films recorded using a JEOL JSM-7600F field emission scanning electron microscope (FESEM), with an accelerating voltage of 5kV. Absorption coefficients at each wavelength were calculated by α(λ) = 1/d * ln([1-R(λ)]/[T(λ)]). Here, α is the absorption coefficient, R is the reflectance, and T is the transmittance. [1]\"\r\n10.1021/acs.chemmater.8b04064,Pyridiniumethylammonium lead iodide,C7H14I4N2Pb,(PyrEA)[PbI4],C7H14N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-pyridin-1-ium,3,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PyrEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,steady-state PL spectroscopy,Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\r\n10.1021/acs.chemmater.8b04064,Imidazoliumethylammonium lead iodide,C5H13I4N3Pb,(ImEA)[PbI4],C5H13N3,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-imidazol-3-ium,2,single crystal,,,,,,,,\"ImEAI, PbI2, HI\",orange plate,\"ImEAI was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and ImEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140ºC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",Single Crystal X-ray Diffraction,\"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo Kα radiation (0.71073Å) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\"\r\n10.1021/acs.chemmater.8b04064,Imidazoliumethylammonium lead iodide,C5H13I4N3Pb,(ImEA)[PbI4],C5H13N3,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-imidazol-3-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,,Wavelength used was λ = 0.71073 Å.\r\n10.1021/acs.chemmater.8b04064,Imidazoliumethylammonium lead iodide,C5H13I4N3Pb,(ImEA)[PbI4],C5H13N3,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-imidazol-3-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,,\r\n10.1021/acs.chemmater.8b04064,Imidazoliumethylammonium lead iodide,C5H13I4N3Pb,(ImEA)[PbI4],C5H13N3,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-imidazol-3-ium,2,film,,,,,,,,\"(ImEA)[PbI4] (synthesized), DMF\",,Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and were spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,Photoluminescence,Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\r\n10.1021/acs.chemmater.8b04064,Imidazoliumethylammonium lead iodide,C5H13I4N3Pb,(ImEA)[PbI4],C5H13N3,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-imidazol-3-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,UV-Vis absorption,Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\r\n10.1021/acs.chemmater.8b04064,Imidazoliumethylammonium lead iodide,C5H13I4N3Pb,(ImEA)[PbI4],C5H13N3,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-imidazol-3-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,,Absorption coefficients at each wavelength were calculated by α(λ) = 1/d(film) * ln([1-Rfilm(λ)]/[Tfilm(λ)])\r\n10.1021/acs.chemmater.8b04064,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PEA)2PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,Optical absorbtion,Wavelength was λ = 0.71073 Å.\r\n10.1021/acs.chemmater.8b04064,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"(PEA)2PbI4 (synthesized), DMF\",,Thin films were prepared by dissolving (PEA)2PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,UV-vis absorption,the spectrum was recorded using SHIMADZU   UV-3600.\r\n10.1021/acs.chemmater.8b04064,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,,,,,,,,,,,,\r\n10.1021/acs.chemmater.8b04064,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,N/A,Thin-film of thickness 338 nm,Thin films were prepared by dissolving (PEA)2PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,UV-Vis spectroscopy and scanning electron microscopy,\"UV-vis absorption spectra were recorded using a SHIMADZU UV-3600 spectrophotometer, with an integrating sphere (ISR-3100) in the wavelength range 300-800nm. Film thickness was calculated by cross-section images of the thin films recorded using a JEOL JSM-7600F field emission scanning electron microscope (FESEM), with an accelerating voltage of 5kV.\r\nAbsorption coefficients at each wavelength were calculated by α(λ) = 1/d * ln([1-R(λ)]/[T(λ)]). Here, α is the absorption coefficient, R is the reflectance, and T is the transmittance. [1]\"\r\n10.1021/acs.chemmater.8b04064,Pyrazoliumethylammonium lead iodide,C20H52I20N12O4Pb6,(PyrzEA)[Pb2I6],C5H13N3,\"Pb2I6, Lead iodide\",1-(2-ethanaminium)-1H-pyrazol-2-ium,1,single crystal,,,,,,,,\"PyrzEAI, PbI2, HI\",yellow prism,\"PipEAI was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and PyrzEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140ºC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",Single Crystal X-ray Diffraction,\"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo Kα radiation (0.71073Å) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\"\r\n10.1021/acs.chemmater.8b04064,Pyrazoliumethylammonium lead iodide,C20H52I20N12O4Pb6,(PyrzEA)[Pb2I6],C5H13N3,\"Pb2I6, Lead iodide\",1-(2-ethanaminium)-1H-pyrazol-2-ium,1,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PyrzEA)[Pb2I6] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,,Wavelength used was λ = 0.71073 Å.\r\n10.1021/acs.chemmater.8b04064,Pyrazoliumethylammonium lead iodide,C20H52I20N12O4Pb6,(PyrzEA)[Pb2I6],C5H13N3,\"Pb2I6, Lead iodide\",1-(2-ethanaminium)-1H-pyrazol-2-ium,1,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PyrzEA)[Pb2I6] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,UV-Vis absorption,Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\r\n10.1021/acs.chemmater.8b04064,Histammonium lead iodide,(C5H11N3)PbI4,\"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",C5H11N3,\"PbI4, Lead iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (HA)PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,,\r\n10.1021/acs.chemmater.8b04064,Histammonium lead iodide,(C5H11N3)PbI4,\"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",C5H11N3,\"PbI4, Lead iodide\",4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide,2,single crystal,,,,,,,,\"histamine dihydrochloride, HI, PbI2\",red block,\"Histamine dihydrochloride was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and HA were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140ºC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",Single Crystal X-ray Diffraction,\"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo Kα radiation (0.71073Å) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\"\r\n10.1021/acs.chemmater.8b04064,piperidiniumethylammonium lead iodide,C14H34I8N4Pb2,(PipEA)[PbI4],C7H20N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-piperidin-1-ium,2,single crystal,,,,,,,,\"PipEAI, PbI2, HI\",red plate,\"PipEAI was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and PipEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140ºC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",Single Crystal X-ray Diffraction,\"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo Kα radiation (0.71073Å) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\"\r\n10.1021/acs.chemmater.8b04064,piperidiniumethylammonium lead iodide,C14H34I8N4Pb2,(PipEA)[PbI4],C7H20N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-piperidin-1-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,,Wavelength used was λ = 0.71073 Å.\r\n10.1021/acs.chemmater.8b04064,piperidiniumethylammonium lead iodide,C14H34I8N4Pb2,(PipEA)[PbI4],C7H20N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-piperidin-1-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,UV-Vis absorption,Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\r\n10.1021/acs.chemmater.8b04064,piperidiniumethylammonium lead iodide,C14H34I8N4Pb2,(PipEA)[PbI4],C7H20N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-piperidin-1-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,steady-state PL spectroscopy,Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\r\n10.1021/acs.chemmater.8b04064,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"Lead(II) iodide, 2-phenethylamine (PEA), HI, diethyl ether\",orange needle-like crystals,\"a round bottom flask containing ethanol and PEA was cooled to 0 degree C. To it, a stoichiometric amount of concentrated hydroiodic acid was added. After stirring the solution for 1 hour, all volatiles were removed using a rotary evaporator. The remaining solid is PEAI salt. It was washed with diethyl ether and dried under vacuum at 50°C overnight.\r\n\r\nStoichiometric amounts of PbI2 and PEAI were added to concentrated stabilized aqueous HI (concentrations of around 0.25-0.30M of Pb2+). The solution was heated and stirred at 140ºC for an hour, and the clear solutions cooled slowly to room temperature.\",Single Crystal X-ray Diffraction,\"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo Kα radiation (0.71073Å) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\"\r\n10.1021/acs.chemmater.8b04064,piperidiniumethylammonium lead iodide,C14H34I8N4Pb2,(PipEA)[PbI4],C7H20N2,\"PbI4, Lead iodide\",1-(2-ethanaminium)-1H-piperidin-1-ium,2,film,,,,,,,,N/A,,Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130ºC for 10 minutes.,steady-state PL spectroscopy,Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\r\n10.1021/acs.chemmater.9b01265,bis(β-methylphenethylammonium) lead iodide,C18H26N2PbI4,\"bis(Œ≤-methylphenylethanaminium) tetraiodoplumbate(II), (Œ≤-Me-PEA)2PbI4, (C9H13N)2PbI4\",C9H13N,\"PbI4, Lead iodide\",bis(β-methylphenylethanaminium) lead (II) iodide,2,powder,,,,,,,,\"β-Methylphenethylamine, lead iodide, hydriodic acid (HI) solution (57 wt %, stabilized, 99.95%)\",Orange crystals,Add stoichiometric amounts of PbI2 (0.25 mmol) and β-Me-PEA (0.5 mmol) into a 3 mL HI solution. Heat the solution to 100 °C to dissolve all solids and then slowly cool at 2 °C/h to room temperature. Collect crystals by filtration and wash with diethyl ether repeatedly.,Powder X-ray diffraction,\"PANalytical Empyrean Powder X-ray diffractometer using Cu Kα radiation, with the X-ray tube operating level at 45 kV and 40 mA.\"\r\n10.1021/acs.chemmater.9b01265,bis(β-methylphenethylammonium) methylammonium lead iodide,C19H32N3Pb2I7,\"bis(Œ≤-methylphenylethanaminium) methanaminium septaiodo diplumbate(II), (Œ≤-Me-PEA)2MAPb2I7, (C9H13N)2CH3NH3Pb2I7\",\"C9H13N, CH6N\",\"Pb2I7, Lead iodide\",bis(β-methylphenylethanaminium) methanaminium lead iodide,2,powder,,,,,,,,\"β-Methylphenethylamine, methylammonium iodide, lead iodide, hydriodic acid (HI) solution (57 wt %, stabilized, 99.95%)\",Red crystals,\"Add PbI2 (1 mmol), MAI (0.5 mmol), and β-Me-PEA (0.25 mmol) into a 1.5 mL HI solution. Heat the solution to 100 °C to dissolve all solids and then slowly cool at 2 °C/h to room temperature. Collect crystals by filtration and wash with diethyl ether repeatedly.\",Powder X-ray diffraction,\"PANalytical Empyrean Powder X-ray diffractometer using Cu Kα radiation, with the X-ray tube operating level at 45 kV and 40 mA.\"\r\n10.1021/acs.chemmater.9b01265,bis(β-methylphenethylammonium) bis(methylammonium) lead iodide,C20H38N4Pb3I10,\"bis(Œ≤-methylphenylethanaminium) bis(methanaminium) decapods triplumbate(II), (Œ≤-Me-PEA)2MA2Pb3I10, (C9H13N)2(CH3NH3)2Pb3I10\",\"C9H13N, CH6N\",\"Pb3I10, Lead iodide\",bis(β-methylphenylethanaminium) bis(methanaminium) lead iodide,2,powder,,,,,,,,\"β-Methylphenethylamine, methylammonium iodide, lead iodide, hydriodic acid (HI) solution (57 wt %, stabilized, 99.95%)\",Deep brown crystals,\"Add PbI2 (1 mmol), MAI (0.667 mmol), and β-Me-PEA (0.065 mmol) into a 1.5 mL HI solution. Heat the solution to 100 °C to dissolve all solids and then slowly cool at 2 °C/h to room temperature. Collect crystals by filtration and wash with diethyl ether repeatedly.\",Powder X-ray diffraction,\"PANalytical Empyrean Powder X-ray diffractometer using Cu Kα radiation, with the X-ray tube operating level at 45 kV and 40 mA.\"\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead iodide,C4N2H12PbI4,\"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",C4N2H12,\"PbI4, Lead iodide\",3-aminopyrrolidinium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",Orange crystals,\"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125ºC, held constant until the crystals formed. The temperature was then decreased to 75º C, at which most crystals formed. The solution was left to cool to room temperature.\",Single-Crystal X-ray Diffraction,\"Samples were collected with a Bruker DUO or Molly instrument with Mo Kα IμS microfocus source (λ= 0.71073 Å) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\"\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead iodide,C4N2H12PbI4,\"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",C4N2H12,\"PbI4, Lead iodide\",3-aminopyrrolidinium lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",Orange crystal,\"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125ºC, held constant until the crystals formed. The temperature was then decreased to 75º C, at which most crystals formed. The solution was left to cool to room temperature.\",UV-vis absorption,The high-energy absorption edge was extrapolated to imaginary axis. This is parallel to the x-axis (absorption edge is interrupted here by low energy exciton peak).\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead iodide,C4N2H12PbI4,\"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",C4N2H12,\"PbI4, Lead iodide\",3-aminopyrrolidinium lead (II) iodide,2,single crystal,SIESTA,DFT,GGA in revPBE form + SOC,3x1x5,,Troullier-Martins pseudpotentials; wave functions: double-ζ polarized basis set of finite-range numerical pseudoatomic orbitals,,\"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",Orange crystal,\"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125ºC, held constant, and crystals formed. Temperature continued to decrease to 75º C, and most crystals began to form. Sample was left to cool to room temperature.\",,\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead chloride,C4N2H12PbCl4,\"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",C4N2H12,\"PbCl4, Lead chloride\",3-aminopyrrolidinium lead (II) chloride,2,single crystal,,,,,,,,\"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"transparent, plate-shaped crystals\",\"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",Single-Crystal X-ray Diffraction,\"Samples were collected with a Bruker DUO or Molly instrument with Mo Kα IμS microfocus source (λ= 0.71073 Å) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\"\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead chloride,C4N2H12PbCl4,\"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",C4N2H12,\"PbCl4, Lead chloride\",3-aminopyrrolidinium lead (II) chloride,2,single crystal,,,,,,,,\"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"transparent, plate-shaped crystals\",\"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",UV-vis absorption,The high-energy absorption edge was extrapolated to imaginary axis. This is parallel to the x-axis (absorption edge is interrupted here by low energy exciton peak).\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead chloride,C4N2H12PbCl4,\"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",C4N2H12,\"PbCl4, Lead chloride\",3-aminopyrrolidinium lead (II) chloride,2,single crystal,SIESTA,DFT,GGA in revPBE form + SOC,5x1x3,,\"Pseudopotentials: Troullier-Martins; •\tWave-functions: over double-ζ polarized basis set of finite-range numerical pseudoatomic orbital\",,\"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"transparent, plate-shaped crystals g.\",\"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in a solution of HI (2.5 mL) and H3PO2 (0.5 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Heat was turned off and crystals formed over several days due to the evaporation of the solvent.\",,\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead bromide,C4N2H12PbBr4,\"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",C4N2H12,\"PbBr4, Lead bromide\",3-aminopyrrolidinium lead (II) bromide,2,single crystal,,,,,,,,\"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"Clear, plate-like crystals\",\"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",Single-Crystal X-ray Diffraction,\"Samples were collected with a Bruker DUO or Molly instrument with Mo Kα IμS microfocus source (λ= 0.71073 Å) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\"\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead bromide,C4N2H12PbBr4,\"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",C4N2H12,\"PbBr4, Lead bromide\",3-aminopyrrolidinium lead (II) bromide,2,single crystal,,,,,,,,\"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"Clear, plate-like crystals\",\"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",Single-Crystal X-ray Diffraction,\"Samples were collected with a Bruker DUO or Molly instrument with Mo Kα IμS microfocus source (λ= 0.71073 Å) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\"\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead bromide,C4N2H12PbBr4,\"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",C4N2H12,\"PbBr4, Lead bromide\",3-aminopyrrolidinium lead (II) bromide,2,bulk polycrystalline,,,,,,,,\"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"Clear, plate-like crystals\",\"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",UV-vis absorption,The high-energy absorption edge was extrapolated to imaginary axis. This is parallel to the x-axis (absorption edge is interrupted here by low energy exciton peak).\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead bromide,C4N2H12PbBr4,\"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",C4N2H12,\"PbBr4, Lead bromide\",3-aminopyrrolidinium lead (II) bromide,2,single crystal,SIESTA,DFT,GGA in revPBE form + SOC,5x1x3,,Pseudopotentials: Troullier-Martins; Wave-functions: over double-ζ polarized basis set of finite-range numerical pseudoatomic orbital,,\"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"Clear, plate-like crystals\",\"First, PbO (2 mmol, 446.4 mg) powder was dissolved in a solution of HBr (2.5 mL) and H3PO2 (0.5 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was shut off and plate crystals formed slowly over evaporation of the solvent\",,\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead iodide,C4N2H12PbI4,\"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",C4N2H12,\"PbI4, Lead iodide\",3-aminopyrrolidinium lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",Orange crystal,\"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125ºC and held constant until the crystals formed. The temperature was then decreased to 75º C, at which most crystals formed. The solution was left to cool to room temperature.\",UV-vis spectroscopy,Shimadzu UV-2600 UV-vis NIR spectrometer (operating at 200-2500nm region) was used at ambient temperature to collect optical diffuse reflectance measurements. BaSO4 was considered a reference. The band gap of the material was estimated with reflectance v. wavelength data and using the Kubelka-Munk equation α/S = (1-R)^{2}(2R)^{-1}.\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead iodide,C4N2H12PbI4,\"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",C4N2H12,\"PbI4, Lead iodide\",3-aminopyrrolidinium lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",Orange crystal,\"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125ºC and held constant until the crystals formed. The temperature was then decreased to 75º C, at which most crystals formed. The solution was left to cool to room temperature.\",Photoluminescence,Samples were excited with wavelength λ = 330nm using an optical parametric amplifier.\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead bromide,C4N2H12PbBr4,\"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",C4N2H12,\"PbBr4, Lead bromide\",3-aminopyrrolidinium lead (II) bromide,2,bulk polycrystalline,,,,,,,,\"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"Clear, plate-like crystals\",\"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",UV-vis spectroscopy,Shimadzu UV-2600 UV-vis NIR spectrometer (operating at 200-2500nm region) was used at ambient temperature to collect optical diffuse reflectance measurements. BaSO4 was considered a reference. Band gap of the material was estimated with reflectance v. wavelength data and using the Kubelka-Munk equation α/S = (1-R)^{2}(2R)^{-1}.\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead bromide,C4N2H12PbBr4,\"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",C4N2H12,\"PbBr4, Lead bromide\",3-aminopyrrolidinium lead (II) bromide,2,bulk polycrystalline,,,,,,,,\"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"Clear, plate-like crystals\",\"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",Photoluminescence,Samples were excited with wavelength λ = 330nm using an optical parametric amplifier.\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead chloride,C4N2H12PbCl4,\"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",C4N2H12,\"PbCl4, Lead chloride\",3-aminopyrrolidinium lead (II) chloride,2,bulk polycrystalline,,,,,,,,\"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"transparent, plate-shaped crystals\",\"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",UV-vis spectroscopy,Shimadzu UV-2600 UV-vis NIR spectrometer (operating at 200-2500nm region) was used at ambient temperature to collect optical diffuse reflectance measurements. BaSO4 was considered a reference. Band gap of the material was estimated with reflectance v. wavelength data and using the Kubelka-Munk equation α/S = (1-R)^{2}(2R)^{-1}.\r\n10.1021/acs.chemmater.9b01511,3-aminopyrrolidinium lead chloride,C4N2H12PbCl4,\"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",C4N2H12,\"PbCl4, Lead chloride\",3-aminopyrrolidinium lead (II) chloride,2,bulk polycrystalline,,,,,,,,\"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\"transparent, plate-shaped crystals\",\"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",Photoluminescence,Samples were excited with wavelength λ = 330nm using an optical parametric amplifier.\r\n10.1021/acs.chemmater.9b01564,Bis(4-fluorophenylmethylammonium) lead iodide,C14H18F2N2PbI4,\"(F-PMA)2PbI4, 4-fluorophenylmethylammonium lead iodide, (C14H18F2N2)PbI4, 4-fluorophenylmethanaminium tetraiodoplumbate(II)\",C7H9FN,\"PbI4, Lead iodide\",4-fluorophenylmethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 57 wt % HI aqueous solution, F-PMA, MeOH\",Dark orange crystal,\"131 mg PbI2 was dissolved in 1ml HI, under stirring at 100 °C for 2 min. Then, 65 mg F-PMA in 1 mL HI and 0.8 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 °C for 2 min before the solution was cooled to room temperature and was left for 12h. \r\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (F-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",Single-Crystal X-ray Diffraction.,\"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 100 K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\"\r\n10.1021/acs.chemmater.9b01564,Bis(4-chlorophenylmethylammonium) lead iodide,C14H18Cl2N2PbI4,\"(Cl-PMA)2PbI4, 4-chlorophenylmethanaminium tetraiodoplumbate(II)\",C7H9ClN,\"PbI4, Lead iodide\",4-chlorophenylmethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 57 wt % HI aqueous solution, Cl-PMA, MeOH\",Orange plate-like crystals,\"124 mg PbI2 was dissolved in 2 ml HI, under stirring at 100 °C for 2 min. Then, 78 mg Cl-PMA in 2 mL HI and 1.2 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 °C for 2 min before the solution was cooled to room temperature and was left for 12h. \r\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (Cl-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",Single-Crystal X-ray Diffraction.,\"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 220K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\"\r\n10.1021/acs.chemmater.9b01564,Bis(4-bromophenylmethylammonium) lead iodide,C14H18Br2N2PbI4,\"(Br-PMA)2PbI4, 4-bromophenylmethanaminium tetraiodoplumbate(II)\",C7H9BrN,\"PbI4, Lead iodide\",4-bromophenylmethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 57 wt % HI aqueous solution, Br-PMA, MeOH\",Orange plate-like crystals,\"127 mg PbI2 was dissolved in 2 ml HI, under stirring at 100 °C for 2 min. Then, 103 mg Br-PMA in 2 mL HI and 1.2 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 °C for 2 min before the solution was cooled to room temperature and was left for 12h. \r\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (Br-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",Single-Crystal X-ray Diffraction.,\"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 100 K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\"\r\n10.1021/acs.chemmater.9b01564,Bis(4-iodophenylmethylammonium) lead iodide,C14H18I2N2PbI4,\"(I-PMA)2PbI4, 4-iodophenylmethanaminium tetraiodoplumbate(II)\",C7H9IN,\"PbI4, Lead iodide\",4-iodophenylmethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 57 wt % HI aqueous solution, I-PMA, MeOH\",Orange plate-like crystal,\"202 mg PbI2 was dissolved in 4 ml HI, under stirring at 100 °C for 2 min. Then, 197 mg I-PMA in 0.3 mL HI and 4 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 °C for 2 min before the solution was cooled to room temperature and was left for 12h. \r\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (Br-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",Single-Crystal X-ray Diffraction.,\"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 100 K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\"\r\n10.1021/acs.chemmater.9b03208,Bis(aminoethyl)-bithiophene lead iodide,C12H18N2S2PbI4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",C12H18N2S2,\"PbI4, Lead iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",2,single crystal,,,,,,,,\"AE2T·HI, PbI2, HI, dimethylformamide\",red crystals,\"First, a solution of PbI2 (3.7 mg) and AE2T·HI (4 mg) was cooled in 2 mL of aqueous HI (57 wt% in H2O, stabilized) and 0.6 mL of dimethylformamide in N2 atmosphere. The solution started from a temperature of 105º C and cooled to room temperature over a time period of 60 hours.\",Single-crystal X-ray diffraction,\"A Bruker APEX II CCD diffractometer at settings 50 kV and 30 mA with MoKα radiation (λ = 0.710 Å) was used to collect data. SAINT program was used to integrate data, and SADABS program was used to correct the absorption.\"\r\n10.1021/acs.chemmater.9b03439,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",Powder film on glass substrate,\"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Diffuse reflectance spectra,Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used. The reflectance was converted to absorbance.\r\n10.1021/acs.chemmater.9b03439,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",Powder film on glass substrate,\"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Photoluminescence spectra,A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the powder films to measure photoluminescence spectra. Excitation was perpendicular to the sample and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\r\n10.1021/acs.chemmater.9b03439,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, butylammonium iodide, anhydrous acetonitrile\",Thin film on glass substrate,\"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \r\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",UV-vis absorption,An Agilent Carry 60 UV-vis instrument was used in transmission mode to measure the absorbance. A blank glass substrate was used as the baseline.\r\n10.1021/acs.chemmater.9b03439,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, butylammonium iodide, anhydrous acetonitrile\",Thin film on glass substrate,\"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \r\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",Photoluminescence Spectra,A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\r\n10.1021/acs.chemmater.9b03439,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",Powder film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste.\r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Photoluminescence Spectra,A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\r\n10.1021/acs.chemmater.9b03439,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,film,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",Thin film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste. \r\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",Photoluminescence Spectra,A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\r\n10.1021/acs.chemmater.9b03439,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",Powder film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste. \r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Diffuse Reflectance Spectra,Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used.\r\n10.1021/acs.chemmater.9b03439,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,film,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate, anhydrous acetonitrile\",Thin film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste. \r\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",UV-vis absorption,An Agilent Carry 60 UV-vis instrument was used in transmission mode to measure the absorbance. A blank glass substrate was used as the baseline.\r\n10.1021/acs.chemmater.9b03439,Bis(benzylammonium) formmamidinium lead iodide,(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4,\"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\"C7H10N, CH5N2\",Lead iodide,bis(benzylaminium) diaminomethanide lead iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",Powder film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Diffuse Reflectance Spectra,Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used.\r\n10.1021/acs.chemmater.9b03439,Bis(benzylammonium) formmamidinium lead iodide,(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4,\"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\"C7H10N, CH5N2\",Lead iodide,bis(benzylaminium) diaminomethanide lead iodide,2,film,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate, anhydrous acetonitrile\",Thin film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \r\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",UV-vis absorption,An Agilent Carry 60 UV-vis instrument was used in transmission mode to measure the absorbance. A blank glass substrate was used as the baseline.\r\n10.1021/acs.chemmater.9b03439,Bis(benzylammonium) formmamidinium lead iodide,(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4,\"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\"C7H10N, CH5N2\",Lead iodide,bis(benzylaminium) diaminomethanide lead iodide,2,film,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate, anhydrous acetonitrile\",Thin film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \r\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",Photoluminescence Spectra,A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\r\n10.1021/acs.chemmater.9b03439,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",Powder film on glass substrate,\"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Diffuse reflectance spectra,Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used. The reflectance was converted to absorbance.\r\n10.1021/acs.chemmater.9b03439,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",Powder film on glass substrate,\"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Photoluminescence spectra,A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the powder films to measure photoluminescence spectra. Excitation was perpendicular to the sample and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\r\n10.1021/acs.chemmater.9b03439,Bis(benzylammonium) formmamidinium lead iodide,(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4,\"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\"C7H10N, CH5N2\",Lead iodide,bis(benzylaminium) diaminomethanide lead iodide,2,powder,,,,,,,,\"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",Powder film on glass substrate,\"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \r\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",Photoluminescence Spectra,A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,single crystal,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\": First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Single-crystal X-ray diffraction,A Rigaku Saturn 724 diffractometer with Mo Kα radiation (λ = 0.71073 Å) was used. Crystal structures were solved by direct methods and refined with the SHELXLTL software.\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,single crystal,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Single-crystal X-ray diffraction,A Rigaku Saturn 724 diffractometer with Mo Kα radiation (λ = 0.71073 Å) was used. Crystal structures were solved by direct methods and refined with the SHELXLTL software.\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,single crystal,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Single-crystal X-ray diffraction,A Rigaku Saturn 724 diffractometer with Mo Kα radiation (λ = 0.71073 Å) was used. Crystal structures were solved by direct methods and refined with the SHELXLTL software.\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,powder,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Differential scanning calorimetry (DSC),PerkinElmer Diamond DSC instrument\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,powder,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Differential scanning calorimetry (DSC),PerkinElmer Diamond DSC instrument\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,powder,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",,\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,powder,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",TGA,A TG209 F3 instrument was used at a heating rate of 10 K per minute.\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,single crystal,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Photoluminescence,An Edinburgh FLS1000 Spectrometer was used to collect data.\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,single crystal,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Photoluminescence excitation,An Edinburgh FLS1000 Spectrometer was used to collect data.\r\n10.1021/acs.inorgchem.0c03008,Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,[(CH3)3PCH2F]CdCl2Br,Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II),C4H11PF,\"CdCl2Br, Cadmium bromide chloride\",Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride,1,pellet,,,,,,,,\"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",rod-like crystals,\"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",Dielectric,A Tonghui TH2828A was used between temperatures 200 to 400 K at 1 MHz with AC voltage of 1 V to find the dielectric constant.\r\n10.1021/acs.inorgchem.5b01896,Bis(methylammonium) copper bromide chloride,(CH3NH3)2CuCl2Br2,\"MA2CuCl2Br2, bis(methanaminium) dibromo dichlorocuprate(II)\",CNH6,\"CuCl2Br2, Copper bromide chloride\",bis(methanaminium) copper bromide chloride,2,single crystal,,,,,,,,\"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water), Hydrobromic acid (48% in water, Sigma-Aldrich), CuCl2 (copper chloride, 99% Sigma-Aldrich), CuBr2 (copper bromide, 99% Sigma-Aldrich)\",MA2CuCl2Br2,\"MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl.\r\nMABr was synthesized by reacting 18 mL of methylamine solution with 8 mL of HBr.\r\n\r\nThe precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h.\",Thermogravimetric analysis (TGA),2950 TGA HR V5.4 (TA Instruments) was used for the TGA analysis under nitrogen flow (40 mL/min).\r\n10.1021/acs.inorgchem.5b01896,Bis(methylammonium) copper bromide chloride,(CH3NH3)2CuCl0.5Br3.5,\"MA2CuCl0.5Br3.5, tetrakis(methanaminium) septabromo monochloro diplumbate(II)\",CNH6,\"CuCl0.5Br3.5, Copper chloride bromide\",bis(methanaminium) copper bromide chloride,2,single crystal,,,,,,,,\"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water), Hydrobromic acid (48% in water, Sigma-Aldrich), CuCl2 (copper chloride, 99% Sigma-Aldrich), CuBr2 (copper bromide, 99% Sigma-Aldrich)\",MA2CuCl0.5Br3.5,MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl. MABr was synthesized by reacting 18 mL of methylamine solution with 8 mL of HBr. The precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h.,Thermogravimetric analysis (TGA),2950 TGA HR V5.4 (TA Instruments) was used for the TGA analysis under nitrogen flow (40 mL/min).\r\n10.1021/acs.inorgchem.5b01896,Methylammonium copper chloride,(CH3NH3)2CuCl4,bis(methanaminium) tetrachlorocuprate,CNH6,\"CuCl4, Copper chloride\",,2,film,,,,,,,,\"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water),  CuCl2 (copper chloride, 99% Sigma-Aldrich), DMSO\",Thin film on glass,\"MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl. The precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h.\r\nThe obtained powder was dissolved in DMSO to prepare a 1 M solution. The solution was spin-coated on glass slides.\",UV-vis absorption,\"UV3600, Shimadzu was used to record the spectra\"\r\n10.1021/acs.inorgchem.5b01896,Bis(methylammonium) copper bromide chloride,(CH3NH3)2CuClBr3,\"MA2CuClBr3, bis(methanaminium) tribromo monochlorocuprate(II)\",CNH6,\"CuClBr3, Copper chloride bromide\",bis(methanaminium) copper bromide chloride,2,film,,,,,,,,\"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water), Hydrobromic acid (48% in water, Sigma-Aldrich), CuCl2 (copper chloride, 99% Sigma-Aldrich), CuBr2 (copper bromide, 99% Sigma-Aldrich), DMSO\",Thin film on glass,MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl. MABr was synthesized by reacting 18 mL of methylamine solution with 8 mL of HBr. The precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h. The obtained powder was dissolved in DMSO to prepare a 1 M solution. The solution was spin-coated on glass slides.,UV-vis absorption,\"UV3600, Shimadzu was used to record the spectra\"\r\n10.1021/acs.inorgchem.6b01336,Bis(4-fluorophenethylammonium) lead iodide,C16H22N2F2PbI4,\"(FPEA)2PbI4,  4-FC6H4(CH2)2NH3+)PbI4, bis(4-fluorophenethanaminium) tetraiodoplumbate(II)\",C8H11NF,\"PbI4, Lead iodide\",bis(4-fluorophenethanaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetone, nitromethane, NaI\",\"orange, plate-shaped crystals\",\"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0º C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60º  C, saturated isopropanol solution was cooled to -10º C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (12 mg, 0.043 mmol) and PbI2 (10 mg, 0.022 mmol) in acetone (10 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added and orange, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",Single crystal X-Ray Diffraction,\"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.7749 Å.\"\r\n10.1021/acs.inorgchem.6b01336,Bis(4-fluorophenethylammonium) methylammonium lead iodide,C17H28N3F2Pb2I7,\"(FPEA)2(MA)Pb2I7, (4-FC6H4(CH2)2NH3+)Pb2I7, bis(4-fluorophenethanaminium) methanaminium septaiodo diplumbate(II)\",\"C8H11NF, CH6N\",\"Pb2I7, Lead iodide\",bis(4-fluorophenethanaminium) methanaminium lead iodide,2,single crystal,,,,,,,,\"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetone, nitromethane, NaI, methylammonium iodide (MAI)\",\"light red, plate-shaped crystals\",\"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0º C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60º  C, saturated isopropanol solution was cooled to -10º C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (5.8 mg, 0.022 mmol), (MA)I (1.7 mg, 0.011 mmol), and PbI2 (10 mg, 0.022 mmol) in acetone (10 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added and light red, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",Single crystal X-Ray Diffraction,\"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.6888 Å.\"\r\n10.1021/acs.inorgchem.6b01336,Bis(4-fluorophenethylammonium) bis(methylammonium) lead iodide,C18H34N4F2Pb3I10,\"(FPEA)2(MA)2Pb3I10, (4-FC6H4(CH2)2NH3+)2(CH3NH3)2Pb3I10, bis(4-fluorophenethanaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C8H11NF, CH6N\",\"Pb3I10, Lead iodide\",bis(4-fluorophenethanaminium) bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetonitrile, nitromethane, NaI, methylammonium iodide (MAI)\",\"dark red, plate-shaped crystals\",\"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0º C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60º  C, saturated isopropanol solution was cooled to -10º C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (3.9 mg, 0.014 mmol), (MA)I (2.3 mg, 0.014 mmol), and PbI2 (10 mg, 0.022 mmol) in acetonitrile (8 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added, and dark red, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",Single crystal X-Ray Diffraction,\"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.7749 Å.\"\r\n10.1021/acs.inorgchem.6b01336,Bis(4-fluorophenethylammonium) bis(methylammonium) lead iodide,C18H34N4F2Pb3I10,\"(FPEA)2(MA)2Pb3I10, (4-FC6H4(CH2)2NH3+)2(CH3NH3)2Pb3I10, bis(4-fluorophenethanaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C8H11NF, CH6N\",\"Pb3I10, Lead iodide\",bis(4-fluorophenethanaminium) bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetonitrile, nitromethane, NaI, methylammonium iodide (MAI)\",\"dark red, plate-shaped crystals\",\"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0º C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60º  C, saturated isopropanol solution was cooled to -10º C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (3.9 mg, 0.014 mmol), (MA)I (2.3 mg, 0.014 mmol), and PbI2 (10 mg, 0.022 mmol) in acetonitrile (8 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added and dark red, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",Single crystal X-Ray Diffraction,\"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.7749 Å.\"\r\n10.1021/acs.inorgchem.6b02764,Trimethylammonium tin iodide,(CH3)3NHSnI3,\"TMASnI3, trimethanaminium triiodostannate(II)\",C3H10N,\"SnI3, Tin iodide\",trimethanaminium tin iodide,1,bulk polycrystalline,,,,,,,,\"SnI2 (synthesized from Sn and I2), (CH3)3N (45% aqueous), HI (99.95% aqueous), and H3PO2 (50% aqueous)\",pale yellow needles,\"(CH3)3NI was prepared by reacting equimolar amounts of (CH3)3N and HI. The entire reaction was performed under N2 atmosphere. SnI2 (372 mg, 1 mmol) was dissolved in aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M) by heating at 130 °C and stirring. To it, (CH3)3NHI (187 mg, 1 mmol) was added. After 5 minutes, the heating and stirring were stopped and the solution was allowed to cool down to room temperature.\",UV-vis absorbance (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Trimethylammonium tin iodide,(CH3)3NHSnI3,\"TMASnI3, trimethanaminium triiodostannate(II)\",C3H10N,\"SnI3, Tin iodide\",trimethanaminium tin iodide,1,unknown,,,,,,,,,,,UV-vis absorption (diffused reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Trimethylammonium tin iodide,(CH3)3NHSnI3,\"TMASnI3, trimethanaminium triiodostannate(II)\",C3H10N,\"SnI3, Tin iodide\",trimethanaminium tin iodide,1,bulk polycrystalline,,,,,,,,\"SnI2 (synthesized from Sn and I2), (CH3)3N (45% aqueous), HI (99.95% aqueous), and H3PO2 (50% aqueous)\",pale yellow needles,\"(CH3)3NI was prepared by reacting equimolar amounts of (CH3)3N and HI. The entire reaction was performed under N2 atmosphere. SnI2 (372 mg, 1 mmol) was dissolved in aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M) by heating at 130 °C and stirring. To it, (CH3)3NHI (187 mg, 1 mmol) was added. After 5 minutes, the heating and stirring were stopped and the solution was allowed to cool down to room temperature.\",UV-vis absorbance (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Trimethylammonium tin iodide,(CH3)3NHSnI3,\"TMASnI3, trimethanaminium triiodostannate(II)\",C3H10N,\"SnI3, Tin iodide\",trimethanaminium tin iodide,1,single crystal,,,,,,,,\"SnI2 (synthesized from Sn and I2), (CH3)3N (45% aqueous), HI (99.95% aqueous), and H3PO2 (50% aqueous)\",pale yellow needles,\"(CH3)3NI was prepared by reacting equimolar amounts of (CH3)3N and HI. The entire reaction was performed under N2 atmosphere. SnI2 (372 mg, 1 mmol) was dissolved in aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M) by heating at 130 °C and stirring. To it, (CH3)3NHI (187 mg, 1 mmol) was added. After 5 minutes, the heating and stirring were stopped, and the solution was allowed to cool down to room temperature.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,1,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",pale yellow needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degas the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (173 mg, 1 mmol) was added to the solution. The crystals started appearing in the solution and the solution was held at 120 °C for 2 h. Following this, the solution was cooled and the crystals were separated.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,1,unknown,,,,,,,,,,,UV-vis absorption (diffused reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,1,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",pale yellow needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degas the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (173 mg, 1 mmol) was added to the solution. The crystals started appearing in the solution and the solution was held at 120 °C for 2 h. Following this, the solution was cooled and the crystals were separated.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,1,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",\"Pale yellow, rectangular needles\",\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (173 mg, 1 mmol) was added to the solution, which created a dense pale-yellow precipitate. Crystals formed immediately and grew inside the mother liquor for 2 hours at 120º C before being washed and collected.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,3,single crystal,,,,,,,,,,,UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",Red crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (1860 mg, 5 mmol) was dissolved in solution, and the flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (865 mg, 5 mmol) was added to the solution, which created a dense pale-yellow precipitate. The hot plate temperature was raised to 200 ºC, leading to the formation of the dark red metastable phase.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Ethylammonium tin iodide,CH3CH2NH3SnI3,\"EASnI3, ethylaminium triiodostannate(II)\",C2H8N,\"SnI3, Tin iodide\",ethylaminium tin iodide,3,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",dark red crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1860 mg, 5 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (865 mg, 5 mmol) was added to the solution, which created a pale-yellow precipitate within 5 minutes. Temperature was raised to 200º C, and precipitate changed to dark red.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Guanidinium tin iodide,C(NH2)3SnI3,\"GASnI3, diaminomethanaminium triiodostannate(II)\",CN3H6,\"SnI3, Tin iodide\",diaminomethanaminium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",Orange hexagonal needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 ºC and was held at the same temperature for 2 h.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Guanidinium tin iodide,C(NH2)3SnI3,\"GASnI3, diaminomethanaminium triiodostannate(II)\",CN3H6,\"SnI3, Tin iodide\",diaminomethanaminium tin iodide,3,unknown,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",Orange hexagonal needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 ºC and was held at the same temperature for 2 h.\",,\r\n10.1021/acs.inorgchem.6b02764,Guanidinium tin iodide,C(NH2)3SnI3,\"GASnI3, diaminomethanaminium triiodostannate(II)\",CN3H6,\"SnI3, Tin iodide\",diaminomethanaminium tin iodide,3,unknown,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",Orange hexagonal needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 ºC and was held at the same temperature for 2 h.\",,\r\n10.1021/acs.inorgchem.6b02764,Guanidinium tin iodide,C(NH2)3SnI3,\"GASnI3, diaminomethanaminium triiodostannate(II)\",CN3H6,\"SnI3, Tin iodide\",diaminomethanaminium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",Orange hexagonal needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 ºC and was held at the same temperature for 2 h.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Guanidinium tin iodide,C(NH2)3SnI3,\"GASnI3, diaminomethanaminium triiodostannate(II)\",CN3H6,\"SnI3, Tin iodide\",diaminomethanaminium tin iodide,3,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\"Dark red (after exposure to air for 30 min, product became black oxidized species).\",\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution, and the solution was then heated at 120º C for 2 hours, then cooled to room temperature.which created a dense pale-yellow precipitate. Solution was stirred for 5 more minutes and then cooled to room temperature.\",\"Dark red (after exposure to air for 30 min, product became black oxidized species).\",\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Guanidinium tin iodide,C(NH2)3SnI3,\"GASnI3, diaminomethanaminium triiodostannate(II)\",CN3H6,\"SnI3, Tin iodide\",diaminomethanaminium tin iodide,2,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\"red, rectangular crystals\",\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (750 mg, 4 mmol) was added to the solution, and the solution was heated to 120º C. The solution then cooled to room temperature, and crystals grew in the mother liquor for 24 hours.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Bis(guanidinium) tin iodide,{C(NH2)3}2SnI4,\"GA2SnI4, bis(diaminomethanaminium) tetraiodostannate(II)\",CN3H6,\"SnI4, Tin iodide\",bis(diaminomethanaminium) tin iodide,2,unknown,,,,,,,,,,,UV-vis absorption (diffused reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Bis(guanidinium) tin iodide,{C(NH2)3}2SnI4,\"GA2SnI4, bis(diaminomethanaminium) tetraiodostannate(II)\",CN3H6,\"SnI4, Tin iodide\",bis(diaminomethanaminium) tin iodide,2,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Bis(guanidinium) tin iodide,{C(NH2)3}2SnI4,\"GA2SnI4, bis(diaminomethanaminium) tetraiodostannate(II)\",CN3H6,\"SnI4, Tin iodide\",bis(diaminomethanaminium) tin iodide,2,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Guanidinium tin iodide,C(NH2)3SnI3,\"GASnI3, diaminomethanaminium triiodostannate(II)\",CN3H6,\"SnI3, Tin iodide\",diaminomethanaminium tin iodide,2,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\"red, rectangular crystals\",\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (750 mg, 4 mmol) was added to the solution, and the solution was heated to 120º C. The solution then cooled to room temperature, and crystals grew in the mother liquor for 24 hours.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\"orange, hexagonal needles\",\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (186 mg, 1 mmol) was added to the solution, and the solution was heated to 120º C. Crystals began to grow and were left to grow at this temperature for 2 hours. Finally, the solution  was cooled to room temperature.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\"orange, hexagonal needles\",\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (186 mg, 1 mmol) was added to the solution, and the solution was heated to 120º C. Crystals began to grow and were left to grow at this temperature for 2 hours. Finally, the solution  was cooled to room temperature.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\"orange, hexagonal needles\",\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (186 mg, 1 mmol) was added to the solution, and the solution was heated to 120º C. Crystals began to grow and were left to grow at this temperature for 2 hours. Finally, the solution  was cooled to room temperature.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",red-orange crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (372 mg, 2 mmol) was added to the solution, and crystals began to grow when stirring was discontinued. Solution cooled, and crystals transformed from red-orange needles to yellow hexagonal plates.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",red-orange crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (372 mg, 2 mmol) was added to the solution, and crystals began to grow when stirring was discontinued. Solution cooled, and crystals transformed from red-orange needles to yellow hexagonal plates.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Acetamidinium tin iodide,CH3C(NH2)2SnI3,\"ACASnI3, Acetamidinium triiodostannate(II)\",C2N2H7,\"SnI3, Tin iodide\",1-aminoethan-1-iminium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",red-orange crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (372 mg, 2 mmol) was added to the solution, and crystals began to grow when stirring was discontinued. Solution cooled, and crystals transformed from red-orange needles to yellow hexagonal plates.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Imidazolium tin iodide,C3N2H5SnI3,\"IMSnI3, imidazolium triiodostannate(II)\",C3N2H5,\"SnI3, Tin iodide\",1H-imidazol-3-ium tin iodide,3,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), imidazole (99%)\",yellow/orange hexagonal plates,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid imidazole (136 mg, 1 mmol) was added to the solution, and the solution was heated to 120º C. Crystals began to grow for 120º C for 2 hours. The solution was then cooled to room temperature.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Imidazolium tin iodide,C3N2H5SnI3,\"IMSnI3, imidazolium triiodostannate(II)\",C3N2H5,\"SnI3, Tin iodide\",1H-imidazol-3-ium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), imidazole (99%)\",yellow/orange hexagonal plates,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid imidazole (136 mg, 1 mmol) was added to the solution, and the solution was heated to 120º C. Crystals began to grow for 120º C for 2 hours. The solution was then cooled to room temperature.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Imidazolium tin iodide,C3N2H5SnI3,\"IMSnI3, imidazolium triiodostannate(II)\",C3N2H5,\"SnI3, Tin iodide\",1H-imidazol-3-ium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Imidazolium tin iodide,C3N2H5SnI3,\"IMSnI3, imidazolium triiodostannate(II)\",C3N2H5,\"SnI3, Tin iodide\",1H-imidazol-3-ium tin iodide,3,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Imidazolium tin iodide,C3N2H5SnI3,\"IMSnI3, imidazolium triiodostannate(II)\",C3N2H5,\"SnI3, Tin iodide\",1H-imidazol-3-ium tin iodide,3,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), imidazole (99%)\",yellow/orange hexagonal plates,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid imidazole (136 mg, 1 mmol) was added to the solution, and the solution was heated to 120º C. Crystals began to grow for 120º C for 2 hours. The solution was then cooled to room temperature.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,[(CH3)2CHNH3]3SnI5,\"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",C3NH10,\"SnI5, Tin iodide\",tris(isopropylaminium) tin iodide,1,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",yellow rectangular needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (561 mg, 3 mmol) was added to the solution, and the solution was heated to 120º C. Stirring stopped, and the solution cool dot room temperature. Crystals precipitated for 24 hours.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,[(CH3)2CHNH3]3SnI5,\"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",C3NH10,\"SnI5, Tin iodide\",tris(isopropylaminium) tin iodide,1,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",yellow rectangular needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (561 mg, 3 mmol) was added to the solution, and the solution was heated to 120º C. Stirring stopped, and the solution cool dot room temperature. Crystals precipitated for 24 hours.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,[(CH3)2CHNH3]3SnI5,\"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",C3NH10,\"SnI5, Tin iodide\",tris(isopropylaminium) tin iodide,1,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,[(CH3)2CHNH3]3SnI5,\"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",C3NH10,\"SnI5, Tin iodide\",tris(isopropylaminium) tin iodide,1,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",yellow rectangular needles,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (561 mg, 3 mmol) was added to the solution, and the solution was heated to 120º C. Stirring stopped, and the solution cool dot room temperature. Crystals precipitated for 24 hours.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,[(CH3)2CHNH3]3SnI5,\"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",C3NH10,\"SnI5, Tin iodide\",tris(isopropylaminium) tin iodide,2,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",Red crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1116 mg, 3 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (1683 mg, 9 mmol) was added to the solution, and a pale-yellow precipitate formed within 5 minutes. The temperature was raised to 200º C, and the precipitate turned red. The solution was cooled and precipitate changed back to yellow.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,{(CH3)2C(H)NH3}3Sn2I7,\"(IPA)3Sn2I7, tris(isopropylaminium) septaiodo distannate(II)\",C3NH10,\"Sn2I7, Tin iodide\",tris(isopropylaminium) tin iodide,2,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,{(CH3)2C(H)NH3}3Sn2I7,\"(IPA)3Sn2I7, tris(isopropylaminium) septaiodo distannate(II)\",C3NH10,\"Sn2I7, Tin iodide\",tris(isopropylaminium) tin iodide,2,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,{(CH3)2C(H)NH3}3Sn2I7,\"(IPA)3Sn2I7, tris(isopropylaminium) septaiodo distannate(II)\",C3NH10,\"Sn2I7, Tin iodide\",tris(isopropylaminium) tin iodide,2,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,[(CH3)2CHNH3]3SnI5,\"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",C3NH10,\"SnI5, Tin iodide\",tris(isopropylaminium) tin iodide,2,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",Red crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1116 mg, 3 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (1683 mg, 9 mmol) was added to the solution, and a pale-yellow precipitate formed within 5 minutes. The temperature was raised to 200º C, and the precipitate turned red. The solution was cooled and precipitate changed back to yellow.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Tris(isopropylammonium) tin iodide,[(CH3)2CHNH3]3SnI5,\"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",C3NH10,\"SnI5, Tin iodide\",tris(isopropylaminium) tin iodide,2,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",Red crystals,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1116 mg, 3 mmol) was dissolved in solution, and flask was heated to boiling (~130 ºC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (1683 mg, 9 mmol) was added to the solution, and a pale-yellow precipitate formed within 5 minutes. The temperature was raised to 200º C, and the precipitate turned red. The solution was cooled and precipitate changed back to yellow.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b02764,Bis(butylammonium) methylammonium tin iodide,CH3(CH2)3(NH3)2(CH3NH3)Sn2I7,\"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\"C4NH12, CNH6\",\"Sn2I7, Tin iodide\",bis(butylaminium) methanaminium tin iodide,2,single crystal,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnCl2·2H2O (98%), CH3NH3Cl (98%), CH3(CH2)3NH2\",cherry-red rectangular plates,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnCl2•2H2O powder (2256 mg, 10 mmol) was dissolved in a solution of 57% (w/w) aqueous HI solution (20 mL, 152 mmol) and 50% aqueous H3PO2 (3.4 mL, 31 mmol) by boiling the solution and constantly stirring. This formed a bright yellow solution. Solid CH3(CH2)3NH2 (694 μL, 7 mmol) was neutralized with 57% (w/w) HI (5 mL38 mmol) via an ice bath. This resulted in a clear pale-yellow solution. CH3(CH2)3NH3I solution was added to SnI2 solution and produced a black precipitate. After the solution was boiled, stirring stopped, the solution cooled, and crystals formed for 2 hours.\",Single crystal X-ray diffraction,\"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 Å), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\"\r\n10.1021/acs.inorgchem.6b02764,Bis(butylammonium) methylammonium tin iodide,CH3(CH2)3(NH3)2(CH3NH3)Sn2I7,\"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\"C4NH12, CNH6\",\"Sn2I7, Tin iodide\",bis(butylaminium) methanaminium tin iodide,2,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnCl2·2H2O (98%), CH3NH3Cl (98%), CH3(CH2)3NH2\",cherry-red rectangular plates,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnCl2•2H2O powder (2256 mg, 10 mmol) was dissolved in a solution of 57% (w/w) aqueous HI solution (20 mL, 152 mmol) and 50% aqueous H3PO2 (3.4 mL, 31 mmol) by boiling the solution and constantly stirring. This formed a bright yellow solution. Solid CH3(CH2)3NH2 (694 μL, 7 mmol) was neutralized with 57% (w/w) HI (5 mL38 mmol) via an ice bath. This resulted in a clear pale-yellow solution. CH3(CH2)3NH3I solution was added to SnI2 solution and produced a black precipitate. After the solution was boiled, stirring stopped, the solution cooled, and crystals formed for 2 hours.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation α/S = (1-R)^{2}/(2R) was used.\r\n10.1021/acs.inorgchem.6b02764,Bis(butylammonium) methylammonium tin iodide,CH3(CH2)3(NH3)2(CH3NH3)Sn2I7,\"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\"C4NH12, CNH6\",\"Sn2I7, Tin iodide\",bis(butylaminium) methanaminium tin iodide,2,unknown,,,,,,,,,,,,\r\n10.1021/acs.inorgchem.6b02764,Bis(butylammonium) methylammonium tin iodide,CH3(CH2)3(NH3)2(CH3NH3)Sn2I7,\"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\"C4NH12, CNH6\",\"Sn2I7, Tin iodide\",bis(butylaminium) methanaminium tin iodide,2,bulk polycrystalline,,,,,,,,\"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnCl2·2H2O (98%), CH3NH3Cl (98%), CH3(CH2)3NH2\",cherry-red rectangular plates,\"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnCl2•2H2O powder (2256 mg, 10 mmol) was dissolved in a solution of 57% (w/w) aqueous HI solution (20 mL, 152 mmol) and 50% aqueous H3PO2 (3.4 mL, 31 mmol) by boiling the solution and constantly stirring. This formed a bright yellow solution. Solid CH3(CH2)3NH2 (694 μL, 7 mmol) was neutralized with 57% (w/w) HI (5 mL38 mmol) via an ice bath. This resulted in a clear pale-yellow solution. CH3(CH2)3NH3I solution was added to SnI2 solution and produced a black precipitate. After the solution was boiled, stirring stopped, the solution cooled, and crystals formed for 2 hours.\",UV-vis absorption (diffuse reflectance),Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\r\n10.1021/acs.inorgchem.6b03095,Dimethylammonium lead iodide,C2H8NPbI3,\"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",C2H8N,\"PbI3, Lead iodide\",\"N,N-dimethanaminium lead (II) iodide\",3,powder,,,,,,,,\"(CH3)2NH, HI, PbI2 and DMAI\",[(CH3)2NH2]PbI3,\"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 was then mixed and ground for 15 min.\",,\r\n10.1021/acs.inorgchem.6b03095,Dimethylammonium lead iodide,C2H8NPbI3,\"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",C2H8N,\"PbI3, Lead iodide\",\"N,N-dimethanaminium lead (II) iodide\",3,powder,,,,,,,,\"(CH3)2NH, HI, PbI2 and DMAI\",[(CH3)2NH2]PbI3,\"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 was then mixed and ground for 15 min.\",,\r\n10.1021/acs.inorgchem.6b03095,Dimethylammonium lead iodide,C2H8NPbI3,\"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",C2H8N,\"PbI3, Lead iodide\",\"N,N-dimethanaminium lead (II) iodide\",1,powder,,,,,,,,\"(CH3)2NH solution (40 wt % in H2O), HI solution (57 wt % in H2O), PbI2 (99%)\",yellow [(CH3)2NH2]PbI3 polycrystalline powder,\"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 were then mixed and ground for 15 min.\",UV−vis spectroscopy (Diffuse reflectance),\"The reflectance spectrum was recorded using a Jasco V-730 UV−visible double-beam spectrophotometer. The Kubelka−Munk equation F(R) = α = (1 − R)^2/ 2R was used to convert reflectance to absorbance; here, R is the reflectance, and α is the absorption coefficients.\"\r\n10.1021/acs.inorgchem.6b03095,Dimethylammonium lead iodide,C2H8NPbI3,\"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",C2H8N,\"PbI3, Lead iodide\",\"N,N-dimethanaminium lead (II) iodide\",1,single crystal,,,,,,,,\"(CH3)2NH solution (40 wt % in H2O), HI solution (57 wt % in H2O), PbI2 (99%)\",yellow needle-shaped [(CH3)2NH2]PbI3 crystals,\"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 were then mixed and ground for 15 min. The obtained yellow powder was dissolved in THF, and the solvent was allowed to evaporate at room temperature.\",Single crystal X-ray diffraction,Data were collected using a Bruker Kappa diffractometer equipped with an APEX II CCD detector using monochromatic Mo Kα radiation (λ = 0.71073 Å).\r\n10.1021/acs.inorgchem.6b03095,Dimethylammonium lead iodide,C2H8NPbI3,\"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",C2H8N,\"PbI3, Lead iodide\",\"N,N-dimethanaminium lead (II) iodide\",1,single crystal,,,,,,,,\"(CH3)2NH solution (40 wt % in H2O), HI solution (57 wt % in H2O), PbI2 (99%)\",yellow needle-shaped [(CH3)2NH2]PbI3 crystals,\"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 were then mixed and ground for 15 min. The obtained yellow powder was dissolved in THF, and the solvent was allowed to evaporate at room temperature.\",Single crystal X-ray diffraction,Data were collected using a Bruker Kappa diffractometer equipped with an APEX II CCD detector using monochromatic Mo Kα radiation (λ = 0.71073 Å).\r\n10.1021/acs.inorgchem.7b00881,Triethylpropylammonium lead iodide,C9H22PbI3,\"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",C9H22,\"PbI3, Lead iodide\",\"N,N,N-triethyl-N-propylaminium lead (II) iodide\",1,single crystal,,,,,,,,\"Triethylpropylammonium iodide, PbI2, and DMF\",yellow rod-like [triethylpropylammonium][PbI3] crystals,0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.,Single crystal X-ray diffraction,Data were recorded using Bruker SMART and the graphite- monochromated Mo Kα (λ = 0.71073 Å) radiation on a CCD area detector.\r\n10.1021/acs.inorgchem.7b00881,Triethylpropylammonium lead iodide,C9H22PbI3,\"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",C9H22,\"PbI3, Lead iodide\",\"N,N,N-triethyl-N-propylaminium lead (II) iodide\",1,single crystal,,,,,,,,\"Triethylpropylammonium iodide, PbI2 and DMF\",yellow rod-like [triethylpropylammonium][PbI3] crystals,0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.,Single crystal X-ray diffraction,Data were recorded using Bruker SMART and the graphite- monochromated Mo Kα (λ = 0.71073 Å) radiation on a CCD area detector.\r\n10.1021/acs.inorgchem.7b00881,Triethylpropylammonium lead iodide,C9H22PbI3,\"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",C9H22,\"PbI3, Lead iodide\",\"N,N,N-triethyl-N-propylaminium lead (II) iodide\",1,single crystal,,,,,,,,\"Triethylpropylammonium iodide, PbI2 and DMF\",yellow rod-like [triethylpropylammonium][PbI3] crystals,0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.,Single crystal X-ray diffraction,Data were recorded using Bruker SMART and the graphite- monochromated Mo Kα (λ = 0.71073 Å) radiation on a CCD area detector.\r\n10.1021/acs.inorgchem.7b00881,Triethylpropylammonium lead iodide,C9H22PbI3,\"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",C9H22,\"PbI3, Lead iodide\",\"N,N,N-triethyl-N-propylaminium lead (II) iodide\",1,single crystal,,,,,,,,\"Triethylpropylammonium iodide, PbI2, and DMF\",yellow rod-like [triethylpropylammonium][PbI3] crystals,0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.,UV-vis absorption,The spectrum was recorded using a PerkinElmer Lambda 950 UV−vis−near-IR spectrophotometer\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylmethylammonium) lead iodide,C14H20N2PbI4,\"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",C7H10N,\"PbI4, Lead iodide\",bis(phenylmethanaminium) lead(II) iodide,2,film,,,,,,,,\"(PMA)2PbI4 crystals, DMF, glass substrates\",Thin-film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(Phenylmethylammonium) lead bromide,C14H20N2PbBr4,\"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",C7H10N,\"PbBr4, Lead bromide\",bis(phenylmethanaminium) lead(II) bromide,2,film,,,,,,,,\"(PMA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylmethylammonium) lead chloride,C14H20N2PbCl4,\"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",C7H10N,\"PbCl4, Lead chloride\",bis(phenylmethanaminium) lead(II) chloride,2,film,,,,,,,,\"(PMA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"(PEA)2PbI4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,film,,,,,,,,\"(PEA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead chloride,C16H24N2PbCl4,\"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",C8H12N,\"PbCl4, Lead chloride\",bis(2-phenylethan-1-aminium) lead (II) chloride,2,film,,,,,,,,\"(PEA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(1-(2-naphthyl)methylammonium) lead bromide,C22H24N2PbBr4,\"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",C11H12N,\"PbBr4, Lead bromide\",1-(2-naphthyl)methylaminium lead(II) bromide,2,film,,,,,,,,\"(NMA)2PbBr4 crystals, DMF, glass substrates\",Thin-film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(1-(2-naphthyl)methylammonium) lead chloride,C22H24N2PbCl4,\"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",C11H12N,\"PbCl4, Lead chloride\",1-(2-naphthyl)methylaminium lead(II) chloride,2,film,,,,,,,,\"(NMA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphthyl)ethanammonium) lead iodide,C24H28N2PbI4,\"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",C12H14N,\"PbI4, Lead iodide\",2-(2-naphthyl)ethane-1-aminium lead(II) iodide,2,film,,,,,,,,\"(NEA)2PbI4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystal into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphtyl)ethanammonium) lead bromide,C24H28N2PbBr4,\"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",C12H14N,\"PbBr4, Lead bromide\",bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide,2,film,,,,,,,,\"(NEA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystal into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphthyl)ethanammonium) lead iodide,C24H28N2PbI4,\"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",C12H14N,\"PbI4, Lead iodide\",2-(2-naphthyl)ethane-1-aminium lead(II) iodide,2,single crystal,,,,,,,,\"PbI2 (99.999% trace metal basis), HI (57 wt % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), CH3OH (>99.9%), 2-(2-naphthyl)ethanamine (NEA, 95%)\",Red and laminar crystals.,Dissolve PbI2 (27.0 mg) in 0.5 mL of HI (57%). Place CH3OH (1 ml) on top of the PbI2 solution. Add 0.020 mL of NEA liquid into the CH3OH layer. Crystals would form in the solution overnight.,Single-crystal X-ray diffraction,Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\r\n10.1021/acs.inorgchem.7b01094,Bis(1-(2-naphthyl)methylammonium) lead bromide,C22H24N2PbBr4,\"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",C11H12N,\"PbBr4, Lead bromide\",1-(2-naphthyl)methylaminium lead(II) bromide,2,single crystal,,,,,,,,\"HBr (48 wt % in H2O, assay >99.99%), 1-(2-Naphthyl)methanamine (95+%) in methanol, PbBr2 (99.999% trace metal basis), DMF\",Colorless and laminar crystals.,Add a stoichiometric amount of 48% concentrated HBr into the NMA methanol solution to prepare NMA·HBr. Evaporate methanol to form colorless NMA·HBr crystals. Separate the crystals. Dissolve NMA·HBr (9.5 mg) and PbBr2 (7.3 mg) into DMF (0.2 mL). Separate the crystals after the partial evaporation of DMF.,Single-crystal X-ray diffraction,Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\r\n10.1021/acs.inorgchem.7b01094,Bis(Phenylmethylammonium) lead bromide,C14H20N2PbBr4,\"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",C7H10N,\"PbBr4, Lead bromide\",bis(phenylmethanaminium) lead(II) bromide,2,single crystal,,,,,,,,\"PbBr2 (99.999% trace metal basis), phenylmethylamine (PMA, >99.0%), HBr (48 wt % in H2O, assay >99.99%), CH3OH (>99.9%)\",Colorless and laminar crystals.,Dissolve PbBr2 (50.3 mg) in 0.5 mL of HBr (48%). Place CH3OH (1 ml) on the top of the PbBr2 solution. Add 0.030 mL of PMA liquid into the CH3OH layer. Expect to form crystals in the solution overnight.,Single-crystal X-ray diffraction,Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2 (99.999% trace metal basis), HI (57 wt % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), CH3OH (>99.9%), 2-phenylethylamine (PEA, 99%)\",Red and laminar crystals.,Dissolve PbI2 (54.6 mg) in 0.5 mL of HI (57%). Place CH3OH (1 ml) on the top of the PbI2 solution. Add 0.030 mL of PEA liquid into the CH3OH layer. Crystals would form in the solution overnight.,Single-crystal X-ray diffraction,Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphtyl)ethanammonium) lead bromide,C24H28N2PbBr4,\"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",C12H14N,\"PbBr4, Lead bromide\",bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"PbBr2 (99.999% trace metal basis), HBr (48 wt % in H2O, assay >99.99%), CH3OH (>99.9%), 2-(2-naphthyl)ethanamine (NEA, 95%)\",Colorless and laminar crystals.,Dissolve PbBr2 (21.5 mg) in 0.5 mL of HBr (48%). Place CH3OH (1 ml) on top of the PbBr2 solution. Add 0.020 mL of NEA liquid into the CH3OH layer. Crystals would form in the solution overnight.,Single-crystal X-ray diffraction,Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead chloride,C16H24N2PbCl4,\"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",C8H12N,\"PbCl4, Lead chloride\",bis(2-phenylethan-1-aminium) lead (II) chloride,2,film,,,,,,,,\"(PEA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphthyl)ethanammonium) lead iodide,C24H28N2PbI4,\"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",C12H14N,\"PbI4, Lead iodide\",2-(2-naphthyl)ethane-1-aminium lead(II) iodide,2,film,,,,,,,,\"(NEA)2PbI4 crystals, DMF, glass substrates\",Thin-film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(1-(2-naphthyl)methylammonium) lead bromide,C22H24N2PbBr4,\"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",C11H12N,\"PbBr4, Lead bromide\",1-(2-naphthyl)methylaminium lead(II) bromide,2,film,,,,,,,,\"(NMA)2PbBr4 crystals, DMF, glass substrates\",Thin-film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He−Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(Phenylmethylammonium) lead bromide,C14H20N2PbBr4,\"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",C7H10N,\"PbBr4, Lead bromide\",bis(phenylmethanaminium) lead(II) bromide,2,film,,,,,,,,\"(PMA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"(PEA)2PbI4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphtyl)ethanammonium) lead bromide,C24H28N2PbBr4,\"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",C12H14N,\"PbBr4, Lead bromide\",bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide,2,film,,,,,,,,\"(NEA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,film,,,,,,,,\"(PEA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylmethylammonium) lead iodide,C14H20N2PbI4,\"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",C7H10N,\"PbI4, Lead iodide\",bis(phenylmethanaminium) lead(II) iodide,2,film,,,,,,,,\"(PMA)2PbI4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylmethylammonium) lead chloride,C14H20N2PbCl4,\"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",C7H10N,\"PbCl4, Lead chloride\",bis(phenylmethanaminium) lead(II) chloride,2,film,,,,,,,,\"(PMA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(1-(2-naphthyl)methylammonium) lead chloride,C22H24N2PbCl4,\"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",C11H12N,\"PbCl4, Lead chloride\",1-(2-naphthyl)methylaminium lead(II) chloride,2,film,,,,,,,,\"(NMA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,Photoluminescence,\"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\"\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead chloride,C16H24N2PbCl4,\"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",C8H12N,\"PbCl4, Lead chloride\",bis(2-phenylethan-1-aminium) lead (II) chloride,2,film,,,,,,,,\"(PEA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylmethylammonium) lead chloride,C14H20N2PbCl4,\"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",C7H10N,\"PbCl4, Lead chloride\",bis(phenylmethanaminium) lead(II) chloride,2,film,,,,,,,,\"(PMA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(1-(2-naphthyl)methylammonium) lead chloride,C22H24N2PbCl4,\"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",C11H12N,\"PbCl4, Lead chloride\",1-(2-naphthyl)methylaminium lead(II) chloride,2,film,,,,,,,,\"(NMA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,film,,,,,,,,\"(PEA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(Phenylmethylammonium) lead bromide,C14H20N2PbBr4,\"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",C7H10N,\"PbBr4, Lead bromide\",bis(phenylmethanaminium) lead(II) bromide,2,film,,,,,,,,\"(PMA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphtyl)ethanammonium) lead bromide,C24H28N2PbBr4,\"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",C12H14N,\"PbBr4, Lead bromide\",bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide,2,film,,,,,,,,\"(NEA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(1-(2-naphthyl)methylammonium) lead bromide,C22H24N2PbBr4,\"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",C11H12N,\"PbBr4, Lead bromide\",1-(2-naphthyl)methylaminium lead(II) bromide,2,film,,,,,,,,\"(NMA)2PbBr4 crystals, DMF, glass substrates\",Thin-film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"(PEA)2PbI4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Visible absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylmethylammonium) lead iodide,C14H20N2PbI4,\"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",C7H10N,\"PbI4, Lead iodide\",bis(phenylmethanaminium) lead(II) iodide,2,film,,,,,,,,\"(PMA)2PbI4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Visible absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(2-(2-naphthyl)ethanammonium) lead iodide,C24H28N2PbI4,\"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",C12H14N,\"PbI4, Lead iodide\",2-(2-naphthyl)ethane-1-aminium lead(II) iodide,2,film,,,,,,,,\"(NEA)2PbI4 crystals, DMF, glass substrates\",Thin-film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(phenylethylammonium) lead chloride,C16H24N2PbCl4,\"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",C8H12N,\"PbCl4, Lead chloride\",bis(2-phenylethan-1-aminium) lead (II) chloride,2,film,,,,,,,,\"(PEA)2PbCl4 crystals, DMF, quartz substrates\",Thin film on quartz,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01094,Bis(Phenylmethylammonium) lead bromide,C14H20N2PbBr4,\"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",C7H10N,\"PbBr4, Lead bromide\",bis(phenylmethanaminium) lead(II) bromide,2,film,,,,,,,,\"(PMA)2PbBr4 crystals, DMF, glass substrates\",Thin film on glass,Dissolve the 2D single crystals into DMF at a concentration 6%∼10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 °C for 10 min before measurement.,UV-Vis absorption,Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead iodide,(C(NH2)3)CsPbI4,\"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",CH6N3,\"CsPbI4, Caesium lead iodide\",diaminomethanaminium caesium lead (II) iodide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",Red crystals,\"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Single-crystal X-ray diffraction,A Bruker Smart Platform diffractometer using an Apex I CCD detector and Mo Kalpha radiation was used for SCXRD. APEX3 software processed the data and the SHELXT and SHELXL programs within the Olex2 package were used to solve and refine the structure.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead iodide,(C(NH2)3)CsPbI4,\"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",CH6N3,\"CsPbI4, Caesium lead iodide\",diaminomethanaminium caesium lead (II) iodide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",Red crystals,\"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",UV-vis absorption,A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calculated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead iodide,(C(NH2)3)CsPbI4,\"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",CH6N3,\"CsPbI4, Caesium lead iodide\",diaminomethanaminium caesium lead (II) iodide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",Red crystals,\"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",UV-vis absorption,A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calculated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead iodide,(C(NH2)3)CsPbI4,\"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",CH6N3,\"CsPbI4, Caesium lead iodide\",diaminomethanaminium caesium lead (II) iodide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",Red crystals,\"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Photoluminescence Spectra,A Joule-Thomson cryostat from MMR Technologies was used to control the temperature in the range of 78 to 300 K. The samples were heated at about 5 K per minute. A 355 nm Nd:YAG laser and a 405 nm CW diode laser were used. An SP-2300 spectrograph from Princeton Instruments was used to record the PL emission that was collimated with an optical fiber. It was also coupled with a CCD array and the spectra were calibrated by using Planck irradiation from a calibrated halogen lamp as reference.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)CsPbBr4,\"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",CH6N3,\"CsPbBr4, Caesium lead bromide\",diaminomethanaminium caesium lead (II) bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow crystals,\"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Single-crystal X-ray diffraction,A Bruker Smart Platform diffractometer using an Apex I CCD detector and Mo Kalpha radiation was used for SCXRD. APEX3 software processed the data and the SHELXT and SHELXL programs within the Olex2 package were used to solve and refine the structure.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)CsPbBr4,\"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",CH6N3,\"CsPbBr4, Caesium lead bromide\",diaminomethanaminium caesium lead (II) bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow crystals,\"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Absorption Spectra,A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)CsPbBr4,\"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",CH6N3,\"CsPbBr4, Caesium lead bromide\",diaminomethanaminium caesium lead (II) bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow crystals,\"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Photoluminescence Spectra,A Joule-Thomson cryostat from MMR Technologies was used to control the temperature in the range of 78 to 300 K. The samples were heated at about 5 K per minute. A 355 nm Nd:YAG laser and a 405 nm CW diode laser were used. An SP-2300 spectrograph from Princeton Instruments was used to record the PL emission that was collimated with an optical fiber. It was also coupled with a CCD array and the spectra were calibrated by using Planck irradiation from a calibrated halogen lamp as reference.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)Cs2Pb2Br7,\"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",CH6N3,\"Cs2Pb2Br7, Caesium lead bromide\",diaminomethanaminium caesium lead bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow needle-like crystals,\"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Single-crystal X-ray diffraction,A Bruker Smart Platform diffractometer using an Apex I CCD detector and Mo Kalpha radiation was used for SCXRD. APEX3 software processed the data and the SHELXT and SHELXL programs within the Olex2 package were used to solve and refine the structure.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)Cs2Pb2Br7,\"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",CH6N3,\"Cs2Pb2Br7, Caesium lead bromide\",diaminomethanaminium caesium lead bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow needle-like crystals,\"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",UV-vis absorption,A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)Cs2Pb2Br7,\"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",CH6N3,\"Cs2Pb2Br7, Caesium lead bromide\",diaminomethanaminium caesium lead bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow needle-like crystals,\"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",UV-vis absorption,A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)CsPbBr4,\"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",CH6N3,\"CsPbBr4, Caesium lead bromide\",diaminomethanaminium caesium lead (II) bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow crystals,\"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Absorption Spectra,A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\r\n10.1021/acs.inorgchem.7b01204,Guanidinium caesium lead bromide,(C(NH2)3)Cs2Pb2Br7,\"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",CH6N3,\"Cs2Pb2Br7, Caesium lead bromide\",diaminomethanaminium caesium lead bromide,2,single crystal,,,,,,,,\"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",Yellow needle-like crystals,\"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",Photoluminescence Spectra,A Joule-Thomson cryostat from MMR Technologies was used to control the temperature in the range of 78 to 300 K. The samples were heated at about 5 K per minute. A 355 nm Nd:YAG laser and a 405 nm CW diode laser were used. An SP-2300 spectrograph from Princeton Instruments was used to record the PL emission that was collimated with an optical fiber. It was also coupled with a CCD array and the spectra were calibrated by using Planck irradiation from a calibrated halogen lamp as reference.\r\n10.1021/acs.inorgchem.7b03217,Heptakis(dimethylammonium) lead bromide,C14H54N7Pb4Br15,\"heptakis(dimethanaminium) pentadecabromo tetraplumbate(II), DMA7Pb4Br15, [(CH3)2NH2]7Pb4Br15\",C2H9N,\"Pb4Br15, Lead bromide\",heptakis(dimethanaminium) lead bromide,2,single crystal,,,,,,,,\"PbBr2 (99%), (CH3)2NH solution (40 wt % in H2O), DMF, HBr solution (48 wt % in H2O)\",Colorless plate-like DMA7Pb4Br15 crystals,\"(CH3)2NH2Br (DMABr) was synthesized by reacting (CH3)2NH with HBr in an ice bath, followed by rotary evaporation, and washed with diethyl ether. 4 mmol of PbBr2 and 7 mmol of DMABr were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature.\",Single crystal X-ray diffraction,Data were recorded using a Bruker Kappa X-ray diffractometer equipped with an Apex II CCD detector and using monochromatic Mo Kα radiation (λ = 0.71073 Å)\r\n10.1021/acs.inorgchem.7b03217,Heptakis(dimethylammonium) lead bromide,C14H54N7Pb4Br15,\"heptakis(dimethanaminium) pentadecabromo tetraplumbate(II), DMA7Pb4Br15, [(CH3)2NH2]7Pb4Br15\",C2H9N,\"Pb4Br15, Lead bromide\",heptakis(dimethanaminium) lead bromide,2,powder,,,,,,,,\"PbBr2 (99%), (CH3)2NH solution (40 wt % in H2O), DMF, HBr solution (48 wt % in H2O)\",Colorless plate-like DMA7Pb4Br15 crystals,\"(CH3)2NH2Br (DMABr) was synthesized by reacting (CH3)2NH with HBr in an ice bath, followed by rotary evaporation, and washed with diethyl ether.\r\n4 mmol of PbBr2 and 7 mmol of DMABr were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature. \r\nThe crystals were ground to prepare the powder.\",UV-vis absorbance (diffuse reflectance),\"Reflectance was recorded using a Jasco V-730 UV−visible double-beam spectrophotometer. The reflectance data were converted to absorbance using the Kubelka−Munk equation: F(R)= α = (1 − R)^2/2R, where R is the reflectance and α is the absorption coefficient.\"\r\n10.1021/acs.inorgchem.7b03217,Heptakis(dimethylammonium) lead chloride,C14H54N7Pb4Cl15,\"heptakis(bimethanaminium) pentadecachloro tetraplumbate(II), DMA7Pb4Cl15, [(CH3)2NH2]7Pb4Cl15\",C2H8N,\"Pb4Cl15, Lead chloride\",heptakis(bimethanaminium) lead chloride,2,single crystal,,,,,,,,\"PbCl2 (99%), (CH3)2NH2Cl (99%) (DMACl), DMF, HCl solution (37 wt % in H2O)\",Colorless DMA7Pb4Cl15 crystals,4 mmol of PbCl2 and 7 mmol of DMACl were mixed in 5 mL of DMF. Single crystals of the final product were obtained after a slow evaporation for a few days at room temperature.,Single crystal X-ray diffraction,Data were recorded using a Bruker Kappa X-ray diffractometer equipped with an Apex II CCD detector and using monochromatic Mo Kα radiation (λ = 0.71073 Å)\r\n10.1021/acs.inorgchem.7b03217,Heptakis(dimethylammonium) lead chloride,C14H54N7Pb4Cl15,\"heptakis(bimethanaminium) pentadecachloro tetraplumbate(II), DMA7Pb4Cl15, [(CH3)2NH2]7Pb4Cl15\",C2H8N,\"Pb4Cl15, Lead chloride\",heptakis(bimethanaminium) lead chloride,2,powder,,,,,,,,\"PbCl2 (99%), (CH3)2NH2Cl (99%) (DMACl), DMF, HCl solution (37 wt % in H2O)\",Colorless DMA7Pb4Cl15 crystals,4 mmol of PbCl2 and 7 mmol of DMACl were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature. The crystals were ground to prepare the powder.,UV-vis absorbance (diffuse reflectance),\"Reflectance was recorded using a Jasco V-730 UV−visible double-beam spectrophotometer. The reflectance data were converted to absorbance using the Kubelka−Munk equation: F(R)= α = (1 − R)^2/2R, where R is the reflectance and α is the absorption coefficient.\"\r\n10.1021/acs.inorgchem.7b03217,Heptakis(dimethylammonium) lead chloride,C14H54N7Pb4Cl15,\"heptakis(bimethanaminium) pentadecachloro tetraplumbate(II), DMA7Pb4Cl15, [(CH3)2NH2]7Pb4Cl15\",C2H8N,\"Pb4Cl15, Lead chloride\",heptakis(bimethanaminium) lead chloride,2,single crystal,,,,,,,,\"PbCl2 (99%), (CH3)2NH2Cl (99%) (DMACl), DMF, HCl solution (37 wt % in H2O)\",Colorless DMA7Pb4Cl15 crystals,4 mmol of PbCl2 and 7 mmol of DMACl were mixed in 5 mL of DMF. Single crystals of the final product were obtained after a slow evaporation for a few days at room temperature.,Photoluminescence,The spectrum was recorded using a Horiba FluoroMax Plus-P spectrofluorometer equipped with an R928P photon-counting emission detector. The excitation source was a 150 W ozone-free Xe arc lamp. A lamp reference correction was applied.\r\n10.1021/acs.inorgchem.7b03217,Heptakis(dimethylammonium) lead bromide,C14H54N7Pb4Br15,\"heptakis(dimethanaminium) pentadecabromo tetraplumbate(II), DMA7Pb4Br15, [(CH3)2NH2]7Pb4Br15\",C2H9N,\"Pb4Br15, Lead bromide\",heptakis(dimethanaminium) lead bromide,2,single crystal,,,,,,,,\"PbBr2 (99%), (CH3)2NH solution (40 wt % in H2O), DMF, HBr solution (48 wt % in H2O)\",Colorless plate-like DMA7Pb4Br15 crystals,\"(CH3)2NH2Br (DMABr) was synthesized by reacting (CH3)2NH with HBr in an ice bath, followed by rotary evaporation, and washed with diethyl ether. 4 mmol of PbBr2 and 7 mmol of DMABr were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature.\",Photoluminescence,The spectrum was recorded using a Horiba FluoroMax Plus-P spectrofluorometer equipped with an R928P photon-counting emission detector. The excitation source was a 150 W ozone-free Xe arc lamp. A lamp reference correction was applied.\r\n10.1021/acs.jpcc.7b00890,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,\"Ab Initio, Quantum Espresso\",DFT,PBE (supplemented by D2 method),4x4x1,\"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",SRL pseudopotentials with Opium,Wave functions have energy cutoff of 680 eV,,,,,\r\n10.1021/acs.jpcc.7b00890,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,\"Ab Initio, Quantum Espresso\",DFT,PBE supplemented by D2 method,4x4x1,\"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",SRL pseudopotentials with Opium,Wave functions have energy cut off of 680 eV,,,,,\r\n10.1021/acs.jpcc.7b00890,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,\"Ab Initio, Quantum Espresso\",DFT,PBE supplemented by D2 method,4x4x1,\"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",SRL pseudopotentials with Opium,Wave functions have energy cut off of 680 eV,,,,,\r\n10.1021/acs.jpcc.7b00890,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,\"Ab Initio, Quantum Espresso\",DFT,PBE supplemented by D2 method,4x4x1,\"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",SRL pseudopotentials with Opium,wave functions have energy cut off of 680 eV,,,,,\r\n10.1021/acs.jpcc.7b00890,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,\"Ab Initio, Quantum Espresso\",DFT,PBE supported by D2 method,4x4x1,\"relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",SRL pseudopotentials with Opium,wave functions have energy cut off of 680 eV,,,,,\r\n10.1021/acs.jpcc.7b00890,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,\"Ab Initio, Quantum Espresso\",DFT,PBE supplemented by D2 method,4x4x4,\"relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",SRL pseudopotentials with Opium,wave functions have energy cut off of 680 eV,,,,,\r\n10.1021/acs.jpclett.6b00248,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,powder,,,,,,,,\"CH3NH3I (MAI, Dyesol), Pb(SCN)2 (Aldrich)\",dark-red (MA)2Pb(SCN)2I2 Powder,Stoichiometric amounts of MAI and Pb(SCN)2 were ground in a nitrogen-filled glovebox. The powdered mixture was then cold-pressed into a pellet. The pellet was flame-sealed under vacuum (∼7 × 10−7 Torr) in a quartz tube. The reaction mixture was slowly heated to 100 °C over 1 h and kept at this temperature for 20 h in a box furnace.,Powder X-ray diffraction,Data was recorded using a PANalytical Empyrean powder X-ray diffractometer (Cu Kα radiation) under ambient conditions with the operating conditions of 40 kV and 44 mA.\r\n10.1021/acs.jpclett.6b00248,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,film,VASP,Density functional theory,HSE,2x6x6,spin-orbit coupling included,\"projector-augmented wave (PAW) method, plane-wave cutoff 500 eV\",total force on each atom converged to <0.01 eV/Å .,\"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",Red crystals,MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.,,\r\n10.1021/acs.jpclett.6b00248,bis(methylammonium) lead thiocyanate iodide,C4H12N4S2PbI2,\"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",CNH6,\"Pb(SCN)2I2, Lead thiocyanate iodide\",bis(methanaminium) lead (II) thiocyanate iodide,2,film,,,,,,,,,,,,\r\n10.1021/acs.jpclett.6b00781,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"PbI2, dimethylformamide, quartz substrate, CH3NH3I (in 0.06 M 2-propanol)\",MAPbI3 film,\"Deposit 1.0 M solution of PbI2 (L0279 for the perovskite precursor, Tokyo Chemical Industry Co. Ltd., Japan) in dehydrated dimethylformamide at 70 °C on a quartz substrate by spin-coating (slope 5 s, 6500 rpm, 5 s, slope 5 s). Anneal the resulting yellow film on a hot plate at 70 °C for 1 h. Dip the PbI2 film in a 0.06 M 2-propanol solution of CH3NH3I (Tokyo Chemical Industry Co., Ltd., Japan) for 40 s. Anneal the formed perovskite film on a hot plate at 70 °C for 1 h. Keep the samples in vacuum at RT for several days before the optical measurements; this process helps to reduce significantly the unreacted PbI2 and subsequently improves the quality of thin film samples.\",Optical-transient absorption,\"Optical transient absorption peak attributed to near-band-edge photocarriers, TA measurements were based on a Yb:KGW regenerative amplified laser (pulse duration: ∼300 fs; repetition rate: 50−100 kHz). Refer to Page 2318 paragraph 1; Figure 2. (a) O-TA.\"\r\n10.1021/acs.jpclett.6b00781,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"PbI2, dimethylformamide, quartz substrate, CH3NH3I (in 0.06 M 2-propanol)\",MAPbI3 film,\"Deposit 1.0 M solution of PbI2 (L0279 for the perovskite precursor, Tokyo Chemical Industry Co. Ltd., Japan) in dehydrated dimethylformamide at 70 °C on a quartz substrate by spin-coating (slope 5 s, 6500 rpm, 5 s, slope 5 s). Anneal the resulting yellow film on a hot plate at 70 °C for 1 h. Dip the PbI2 film in a 0.06 M 2-propanol solution of CH3NH3I (Tokyo Chemical Industry Co., Ltd., Japan) for 40 s. Anneal the formed perovskite film on a hot plate at 70 °C for 1 h. Keep the samples in vacuum at RT for several days before the optical measurements; this process helps to reduce significantly the unreacted PbI2 and subsequently improves the quality of thin film samples.\",Photoluminescence,PL measurements were based on a Yb:KGW regenerative amplified laser (pulse duration: ∼300 fs; repetition rate: 50−100 kHz) with 1.8 eV photoexcitation. O-PL peak emerged under strong fluences. Refer to Page 2317 paragraph 3; Figure 1. (a) O-PL.\r\n10.1021/acs.jpclett.6b00781,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"PbI2, dimethylformamide, quartz substrate, CH3NH3I (in 0.06 M 2-propanol)\",MAPbI3 film,\"Deposit 1.0 M solution of PbI2 (L0279 for the perovskite precursor, Tokyo Chemical Industry Co. Ltd., Japan) in dehydrated dimethylformamide at 70 °C on a quartz substrate by spin-coating (slope 5 s, 6500 rpm, 5 s, slope 5 s). Anneal the resulting yellow film on a hot plate at 70 °C for 1 h. Dip the PbI2 film in a 0.06 M 2-propanol solution of CH3NH3I (Tokyo Chemical Industry Co., Ltd., Japan) for 40 s. Anneal the formed perovskite film on a hot plate at 70 °C for 1 h. Keep the samples in vacuum at RT for several days before the optical measurements; this process helps to reduce significantly the unreacted PbI2 and subsequently improves the quality of thin film samples.\",Photoluminescence,PL measurements were based on a Yb:KGW regenerative amplified laser (pulse duration: ∼300 fs; repetition rate: 50−100 kHz) with 1.8 eV photoexcitation. T-PL peak visible at low fluences. Refer to Page 2317 paragraph 3; Figure 1. (a) T-PL.\r\n10.1021/acs.jpclett.6b02682,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,3,powder,,,,,,,,\"Indium chloride (InCl3, Sigma-Aldrich, 99.99%), Silver chloride (AgCl, Sigma-Aldrich, 99%), HCl, Cesium chloride (CsCl, Sigma-Aldrich, 99.9%)\",White powder,Mix 1 mmol InCl3 and AgCl in 5 mL 10 M HCl. Add 2 mmol of CsCl and heat the solution to 115 °C. Leave the hot solution for 30 min under gentle stirring to ensure a complete reaction before filtering. Wash the resulting solid with ethanol and dry in a furnace overnight at 100 °C.,Powder X-ray diffraction,Panalytical X’pert diffractometer (Cu−Kα1 radiation; λ = 154.05 pm) at room temperature. Structural parameters were obtained by Rietveld refinement.\r\n10.1021/acs.jpclett.6b02682,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,3,single crystal,Quantum ESPRESSO,DFT,LDA,Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid,,Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density,10−3 Ry threshold for convergence of forces; 10−4 Ry threshold for total energy,,,,,\r\n10.1021/acs.jpclett.6b02682,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,3,single crystal,Quantum ESPRESSO,DFT,PBE,Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid,,Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density,10−3 Ry threshold for convergence of forces; 10−4 Ry threshold for total energy,,,,,\r\n10.1021/acs.jpclett.6b02682,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,3,single crystal,Quantum ESPRESSO,DFT,HSE,Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid,,Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density,10−3 Ry threshold for convergence of forces; 10−4 Ry threshold for total energy,,,,,\r\n10.1021/acs.jpclett.6b02682,Cesium silver indium bromide,Cs2InAgBr6,Dicesium tribromoargentate(I) tribromoindiate(III),None,InAgBr6,,3,single crystal,Quantum ESPRESSO,DFT,LDA,Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid,,Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density,10−3 Ry threshold for convergence of forces; 10−4 Ry threshold for total energy,,,,,\r\n10.1021/acs.jpclett.6b02682,Cesium silver indium iodide,Cs2InAgI6,Dicesium triiodoargentate(I) triiodoindiate(III),None,InAgI6,,3,single crystal,Quantum ESPRESSO,DFT,LDA,Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid,,Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density,10−3 Ry threshold for convergence of forces; 10−4 Ry threshold for total energy,,,,,\r\n10.1021/acs.jpclett.7b02322,bis(methylammonium) potassium gadolinium chloride,C2H12N2KGdCl6,\"(MA)2KGdCl6, (CH3NH3)2KGdCl6, bis(methanaminium) trichlorogadoliniate(III) tripotassiate(I)\",CH6N,\"KGdCl6, Potassium chloride gadolinium\",bis(methanaminium) potassium gadolinium chloride,0,single crystal,VASP,DFT,optB86b-vdW,,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.7b02322,bis(methylammonium) potassium yttrium chloride,C2H12N2KYCl6,\"(MA)2KYCl6, (CH3NH3)2KYCl6, bis(methanaminium) trichloropotassiate(I) trichloroyttriate(III)\",CH6N,\"KYCl6, Potassium chloride yttrium\",bis(methanaminium) potassium yttrium chloride,3,single crystal,VASP Package,DFT (van der Waals-corrected),\"Van der Waals density functional method (optB86b-vdW); specifically, PBE, (PBE+D2 and PBE+D3), (PBE+TS), PBEsol.\",,,PAW,,\"Y2O3, KCl, (MA)Cl, HCl\",\"clear, colorless crystals\",\"Y2O3 (1 mmol), KCl (1 mmol), and (MA)Cl (2 mmol) were dissolved in 2 mL of HCl solution (32 wt %). The solution was placed in a covered, glass vial on a hot place at 80º, stirred for one hour at this temperature (until the solution became clear), and the cap was finally opened. The solution evaporated until dry at 85º. Crystals were selected from the dry sample.\",Variable Temperature Single Crystal X-ray Diffraction (VT-SCXRD),\"Crystals were selected for further analysis, placed on an Xcalibur/Gemini Ultra diffractometer with an Eos CCD area detector via Paratone-N. Structures were solved via direct methods via Olex 2 and ShelXS structure solution program. They were further refined with ShelXL refinement package.\"\r\n10.1021/acs.jpclett.7b02322,bis(methylammonium) potassium yttrium chloride,C2H12N2KYCl6,\"(MA)2KYCl6, (CH3NH3)2KYCl6, bis(methanaminium) trichloropotassiate(I) trichloroyttriate(III)\",CH6N,\"KYCl6, Potassium chloride yttrium\",bis(methanaminium) potassium yttrium chloride,3,single crystal,VASP,DFT,optB86b-vdW,,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.7b02322,bis(methylammonium) potassium gadolinium chloride,C2H12N2KGdCl6,\"(MA)2KGdCl6, (CH3NH3)2KGdCl6, bis(methanaminium) trichlorogadoliniate(III) tripotassiate(I)\",CH6N,\"KGdCl6, Potassium chloride gadolinium\",bis(methanaminium) potassium gadolinium chloride,0,single crystal,,,,,,,,\"Gd2O3, KCl, (MA)Cl, HCl\",Colorless single crystals,\"Y2O3 or Gd2O3, KCL, and (MA)Cl were dissolved in an HCl solution inside a capped glass vial. It was held at 80 degrees Celsius and stirred for one hour, becoming clear and colorless. The cap was opened, and the solution was evaporated at 85 degrees leaving behind crystals.\",Single-crystal X-ray diffraction,The frames were collected using an Xcalibur/Gemini Ultra diffractometer and an Eos CCD area detector.\r\n10.1021/acs.jpclett.7b02322,bis(methylammonium) potassium yttrium chloride,C2H12N2KYCl6,\"(MA)2KYCl6, (CH3NH3)2KYCl6, bis(methanaminium) trichloropotassiate(I) trichloroyttriate(III)\",CH6N,\"KYCl6, Potassium chloride yttrium\",bis(methanaminium) potassium yttrium chloride,3,single crystal,,,,,,,,\"Y2O3, KCl, (MA)Cl, HCl\",Colorless single crystals,\"Y2O3 or Gd2O3, KCL, and (MA)Cl were dissolved in an HCl solution inside a capped glass vial. It was held at 80 degrees Celsius and stirred for one hour, becoming clear and colorless. The cap was opened, and the solution was evaporated at 85 degrees leaving behind crystals.\",Single-crystal X-ray diffraction,The frames were collected using an Xcalibur/Gemini Ultra diffractometer and an Eos CCD area detector.\r\n10.1021/acs.jpclett.7b03229,Guanidinium zinc fomate,CH6N3ZnC3HHO6,\"[Gua][Zn(HCOO)3], [C(NH2)3][Zn(HCOO)3]\",CH6N3,\"[Zn(HCOO)3]-, Zinc formate\",Guanidinium zinc fomate,3,single crystal,,,,,,,,,,,Single crystal X-ray diffraction,\"Frames were collected using an Oxford Gemini single-crystal diffractometer using Mo radiation (λ = 0.71073 Å, operating at 50 kV and 40 mA)\"\r\n10.1021/acs.jpclett.7b03229,Guanidinium copper fomate,CH6N3CuC3HHO6,\"[Gua][Cu(HCOO)3], [C(NH2)3][Cu(HCOO)3]\",CH6N3,\"[Cu(HCOO)3]-, Copper formate\",Guanidinium copper fomate,3,single crystal,,,,,,,,,,,Single crystal X-ray diffraction,\"Frames were collected using an Oxford Gemini single-crystal diffractometer using Mo radiation (λ = 0.71073 Å, operating at 50 kV and 40 mA).\"\r\n10.1021/acs.jpclett.8b03717,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,3,single crystal,VASP,DFT,GW0,4x4x4,scalar,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,3,single crystal,VASP,DFT,BSE,16x16x16,scalar,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,single crystal,VASP,DFT,GW0,4x3x1,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,single crystal,VASP,DFT,BSE,16x12x4,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,single crystal,CP2K,DFT,PBE-SIC,,scalar,Gaussian+PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N, N′-dimethylethylenediamine lead bromide\",C4H14N2PbBr4,\"N, N‚Ä≤-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N, N′-dimethylethylenediaminium lead (II) bromide\",1,single crystal,VASP,DFT,GW0,2x4x2,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N, N′-dimethylethylenediamine lead bromide\",C4H14N2PbBr4,\"N, N‚Ä≤-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N, N′-dimethylethylenediaminium lead (II) bromide\",1,single crystal,VASP,DFT,GW0,2x4x2,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N, N′-dimethylethylenediamine lead bromide\",C4H14N2PbBr4,\"N, N‚Ä≤-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N, N′-dimethylethylenediaminium lead (II) bromide\",1,single crystal,VASP,DFT,GW0,2x4x2,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N, N′-dimethylethylenediamine lead bromide\",C4H14N2PbBr4,\"N, N‚Ä≤-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N, N′-dimethylethylenediaminium lead (II) bromide\",1,single crystal,CP2K,DFT,PBE-SIC,,scalar,Gaussian+PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,Cesium tin bromide (0D),Cs4SnBr6,tetracesium hexabromostannate(II),None,\"SnBr6, Tin bromide\",,0,single crystal,CP2K,DFT,PBE0,2x2x2,scalar,Gaussian+PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,Cesium tin bromide (0D),Cs4SnBr6,tetracesium hexabromostannate(II),None,\"SnBr6, Tin bromide\",,0,single crystal,CP2K,DFT,PBE0,2x2x2,scalar,Gaussian+PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,Cesium tin bromide (0D),Cs4SnBr6,tetracesium hexabromostannate(II),None,\"SnBr6, Tin bromide\",,0,single crystal,CP2K,DFT,PBE0,2x2x2,scalar,Gaussian+PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,Cesium tin bromide (0D),Cs4SnBr6,tetracesium hexabromostannate(II),None,\"SnBr6, Tin bromide\",,0,single crystal,CP2K,DFT,PBE0,2x2x2,scalar,Gaussian+PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,single crystal,VASP,DFT,GW0,4x3x1,SOC,PAW,,,,,,\r\n10.1021/acs.jpclett.8b03717,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,3,single crystal,VASP,DFT,GW0,4x4x4,scalar,PAW,,,,,,\r\n10.1021/acs.jpclett.9b00247,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"HI (Sigma Aldrich, 57% w/w), chloroform (Fisher, HPLC grade), tributylphosphate (Acros Organics, 99+%), PbI2 (Strem, 99.999+%), phenylethylamine (PEA, Sigma-Aldrich, >99.5%), diethyl ether (Fisher, ACS grade, anhydrous, stabilized with BHT)\",orange crystals,\"7 ml Unstabilized HI was treated with 10% v/v solution of tributylphosphate in chloroform. The aqueous phase (HI) was extracted.\r\nPbI2 (.231 g) was dissolved in the HI solution by heating to 100º C under N2 flow. In it, 0.13 ml PEA is added. The reaction is then cooled to room temperature, at a constant rate of 2 ºC/h. Then, the mixture is cooled at 4ºC for 30 minutes, filtered, washed with diethyl ether, and dried overnight under vacuum at 50 °C.\",Single crystal X-Ray Diffraction,SCXRD data are collected on a Bruker Kappa APEX II DUO diffractometer with a CCD area detector employing graphite-monochromated Mo Kα radiation (λ = 0.710 73 Å). Crystals for SCXRD measured at 100 K are cooled by an Oxford Cryostream.\r\n10.1021/acs.jpclett.9b00247,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"HI (Sigma Aldrich, 57% w/w), chloroform (Fisher, HPLC grade), tributylphosphate (Acros Organics, 99+%), PbI2 (Strem, 99.999+%), phenylethylamine (PEA, Sigma-Aldrich, >99.5%), diethyl ether (Fisher, ACS grade, anhydrous, stabilized with BHT)\",orange crystals,\"7 ml Unstabilized HI was treated with 10% v/v solution of tributylphosphate in chloroform. The aqueous phase (HI) was extracted. PbI2 (.231 g) was dissolved in the HI solution by heating to 100º C under N2 flow. In it, 0.13 ml PEA is added. The reaction is then cooled to room temperature, at a constant rate of 2 ºC/h. Then, the mixture is cooled at 4ºC for 30 minutes, filtered, washed with diethyl ether, and dried overnight under vacuum at 50 °C.\",Single crystal X-Ray Diffraction,SCXRD data are collected on a Bruker Kappa APEX II DUO diffractometer with a CCD area detector employing graphite-monochromated Mo Kα radiation (λ = 0.710 73 Å).\r\n10.1021/acsaem.8b01809,\"Hexane-1,6-diammonium bismuth iodide\",C6H18N2BiI5,\"(HDA)BiI5, C6H18BiI5N2, hexane-1,6-diaminium pentaiodo bismuthate(III)\",C6H18N2,\"BiI5, Bismuth iodide\",\"hexane-1,6-diaminium bismuth iodide\",1,single crystal,,,,,,,,\"HDAI2, BiI3, DCM, DMF, DMSO\",Red single crystals,\"Single crystals of (HDA2+)BiI5 were grown by vapor diffusion of dichloromethane (DCM) into a 0.5 M solution of 1:1 molar ratio hexane-1,6-diamine dihydriodide (HDAI2):BiI3 in a solvent mixture of 4:1 (volume ratio) N,N-dimethylformamide (DMF):dimethyl sulfoxide (DMSO), and with HDAI2 in slight excess to ensure there was no residual BiI3.\",Single-crystal X-ray diffraction,\"XRD measurements made by a Bruker SMART APEX II diffractometer. The APEX2 program packages was used to determine unit-cell parameters and for data collection. Raw frame data was process with SAINT and SADABS for the reflection data file, and further calculations were performed with the SHELXTL program.\"\r\n10.1021/acsaem.8b01809,Tris(N-propylammonium) bismuth iodide,C12H36N3Bi2I9,\"(PA)3Bi2I9, N-propylammonium bismuth iodide, tris(N-propane-1-aminium) nonaiodobismuthate(III)\",C4H12N,\"Bi2I9, Bismuth iodide\",tris(N-propane-1-aminium) bismuth iodide,0,single crystal,,,,,,,,\"PAI, BiI3, DCM, CH3OH\",Orange plate-like crystals,\"Single crystals of (PA+)xBiI3+x were grown by vapor diffusion of dichloromethane (DCM) into a 0.5 M solution of 2:1 molar ratio n-propylamine hydriodide (PAI):BiI3 in methanol, with PAI in slight excess to ensure there was no residual BiI3. For single-crystal growth of (PA+)xBiI3+x, methanol (CH3OH) was chosen as the solvent because single crystals grown in a solvent mixture of 4:1 (v/v) DMF:DMSO were not large enough for single-crystal diffraction measurements.\",Single-crystal X-ray diffraction,\"XRD measurements made by a Bruker SMART APEX II diffractometer. The APEX2 program packages was used to determine unit-cell parameters and for data collection. Raw frame data was process with SAINT and SADABS for the reflection data file, and further calculations were performed with the SHELXTL program.\"\r\n10.1021/acsaem.9b00419,Azetidinium lead bromide,C3H8Br3NPb,\"AzPbBr3, methanaminium tribromoplumbate(II)\",C3H8N,\"PbBr3, Lead bromide\",Azetidinium lead bromide,3,single crystal,,,,,,,,\"AzBr (synthesized from AzCl (0.94 g, 10 mmol, 1 equiv.) and NaBr (2.05g, 20 mmol, 2 equiv.)), PbBr2, DMF/DMSO (4:1), Acetonitrile\",Pale yellow needle-like crystals,AzPbBr3 was prepared by mixing AzBr with PbBr2 in DMF/DMSO (4:1) solution by stirring for 2 h. Acetonitrile was added slowly into the solution and left to stand for 10 min before filtration. The resulting powder was filtered and washed.,Thermogravimetric analysis (TGA),An analysis of the single crystals of AzPbBr3 was performed using TGA via an Integrated Thermo-gravimetric Analyzer (TGA/DTA3600). The data for AzPbBr3 via a thermogravimetric analysis was obtained from room temperature to 700 °C.\r\n10.1021/acsaem.9b00419,Azetidinium methylammonium lead bromide,C3H8Br3NPb,\"Azetidinium lead bromide, Az0.4MA0.6PbBr3, azetidinium methanaminium tribromoplumbate(II)\",C3H8N,\"PbBr3, Lead bromide\",azetidinium methanaminium lead bromide,3,single crystal,,,,,,,,\"AzCl, NaBr, DMF/DMSO\",Az0.4MA0.6PbBr3,\"Ion exchanged between AzCl and NaBr was performed to yield AzBr, which was then later dried in DMF/DMSO (4:1) solvents with PbBr2 to produce Az0.4MA0.6PbBr3. The crystals were obtained via slow diffusion of the antisolvent chloroform, which was dissolved in DMF.\",Absorbance spectra,\"Using the UV-VIS spectrometer, the absorption for AzPbBr3 ( single crystal) and MAPbBr3 powders were obtained. The absorption spectra were recorded using a JASCO-V650 double beam spectrophotometer and the bandgap was determined using the Band-Gap Calculation program in the spectrophotometer. The spectroscopy data were collected over the frequency of 100 Hz, an excitation of 100 mV, collected at 2 K increments at a heating/cooling rate of 1 K min-1 between 50 and 473 K, and used a closed cycle cryocooler.\"\r\n10.1021/acsami.1c20234,Phenethylammonium silver indium bromide,(C6H5(CH2)2NH3)4AgInBr8,\"(PEA)4AgInBr8, tetra(1-phenyl-2-aminoethane) tetrabromoargentate(I) tetrabromoindiate(III)\",C8NH12,AgInBr8,tetra(1-phenyl-2-aminoethane) silver indium octabromide,2,single crystal,,,,,,,,\"PEABr, AgBr, InBr3\",transparent plate-like crystals,\"15 ml HBr was added to PEABr (0.777 g), AgBr (0.182 g) and InBr3 (0.341 g). The solution was heated to 90° while being magnetically stirred until clear. The clear solution was cooled at approx. 2°/hour until at room temperature.\",SCXRD,\"Single crystal X-ray diffraction using Rigaku Oxford diffractometer, Mo Kα Radiation.\"\r\n10.1021/acsami.1c20234,i-butylammonium silver indium bromide,(CH(CH3)2CH2NH3)4AgInBr8,\"(i-BA)4AgInBr8, tetra(1-amino-2-methylpropane) tetrabromoargentate(I) tetrabromoindiate(III)\",C4NH9,AgInBr8,tetra(1-amino-2-methylpropane) silver indium octabromide,2,single crystal,,,,,,,,\"i-BABr, AgBr, InBr3\",transparent plate-like crystals,\"3.0 ml HBr was added to i-BABr (0.638 g), AgBr (0.195 g), and InBr3 (0.367 g). The solution was heated to 90° while being magnetically stirred until clear. The clear solution was cooled at approx. 2°/hour until at room temperature.\",Single crystal X-ray diffraction,\"Single crystal X-ray diffraction using Rigaku Oxford diffractometer, Mo Kα Radiation,\"\r\n10.1021/acsami.7b12862,\"tetrakis(N,N′-dimethylethylene-1,2-diammonium-bromo) tin bromide iodide\",(C16H52N8Br4SnBr3I3,\"tetrakis(N,N‚Ä≤-dimethylethylene-1,2-diaminium-bromo) tribromo-triiodostannate(II)\",C4H14N2Br,\"SnBr3I3, Tin bromide iodide\",\"tetrakis(N,N′-dimethylethylene-1,2-diaminium-bromo) tin bromide iodide\",0,single crystal,,,,,,,,\"Tin (II) bromide, Tin (II) iodide, N,N’-dimethylethylenediamine (99 %), hydrobromic acid (48 wt. % in H2O), hydriodic acid (55%), dichloromethane (DCM, 99.9 %), dimethylformamide (DMF, 99.8 %), toluene (anhydrous, 99.8 %)\",Large yellow crystals,\"To prepare N,N’-dimethylethylene-1,2-diammonium bromide salts, add hydrobromic acid solution (2.2 equiv, 48%) into N,N’ dimethylethylenediamine (1 equiv) in ethanol at 0 C. Remove the solvents and starting reagents under vacuum, and wash the residue with ethyl ether. Dry salts and keep in a desiccator for future use. Prepare N,N’-dimethylethylene-1,2-diammonium iodide salts in a similar manner.\r\n\r\nTo prepare (C4N2H14Br)4SnBr3I3, mix tin(II) bromide and N,N’-dimethylethylene-1,2-diammonium bromide at 1:4 molar ratio and dissolve in DMF to form a clear solution. Mix tin(II) iodide and N,N’-dimethylethylene-1,2-diammonium iodide at 1:4 molar ratio and dissolve in DMF to form another clear solution. Mix bromide and iodide solutions at 1:1 to form a precursor solution. Prepare bulk single crystal by diffusing DCM into DMF solution at room temperature overnight. Wash the large yellowish crystals with acetone and dry under reduced pressure.\",Single crystal X-ray diffraction,\"Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation. \r\nMounted in a cryoloop under Paratone-N oil and cooled to 120 K with an Oxford-Diffraction Cryojet. \r\nPost processing: Oxford-Diffraction CrysAlisPro software, CRYSTALS.\"\r\n10.1021/acsenergylett.8b00661,\"N, N′-dimethylethylenediamine lead chloride\",C4H14N2PbCl4,\"N, N‚Ä≤-dimethylethylenediaminium tetrachloroplumbate(II)\",C4H14N2,\"PbCl4, Lead chloride\",\"N, N′-dimethylethylenediaminium lead (II) chloride\",1,single crystal,,,,,,,,\"Hydrochloric acid (HCl, 37 wt. % in H2O), N, N’-dimethylethylenediamine (99%), Lead (II) chloride (PbCl2, 99.99%)\",Colorless platelet-like crystals,\"To grow C4N2H14PbCl4 single crystals, dissolve lead (II) chloride (150 mg, 0.54 mmol) and N, N’-dimethylethylene-1,2-diammonium chloride (43.7 mg, 0.27 mmol) in DMSO to form a clear precursor solution. Diffuse single crystal into precursor solution for one day. Wash with acetone and dry in vacuum.\",Single crystal X-ray diffraction,\"Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation. \r\nCool to 100 K with an Oxford-Diffraction Cryojet. \r\nPost-processing: Oxford-Diffraction CrysAlisPro software, CRYSTALS13, employing Superflip14 to solve the crystal structure.\"\r\n10.1021/acsomega.8b02877,tetrakis((R)-1-phenylethylammonium) bismuth bromide,C32H48N4Bi2Br10,\"(R)-(MBA)4[BiBr10], (R)-1-phenylethylammonium bromobismuthate(III), [((R)-C8H12N)4][Bi2Br10]\",C8H12N,\"Bi2Br10, Bismuth bromide\",tetrakis((R)-1-phenylethylammonium) bismuth bromide,0,single crystal,,,,,,,,\"(R)-(+)-1-Phenylethylamine ((R)-1-PEA,  >99%), N,N′-dimethylformamide (DMF, anhydrous, 99.9%), bismuth-(III) bromide (BiBr3, 99.9%), and hydrobromic acid (HBr, 48 wt %)\",Yellow large plate-like crystals,\"[((R)-C8H12N)4]-[Bi2Br10][(R)-1] was grown through a slow evaporation method. BiBr3 (0.8 x 10^{−3} mol, 0.359 g) and (R)-1- phenylethylamine (1.6 x 10^{−3} mol, 0.206 mL) were dissolved in 6 mL of a 48% HBr aqueous solution. The solution mixture was heated at 60 °C for 20 min and slowly cooled to room temperature. Yellow crystals of compounds (R)-1 were grown in 2 days as the solvent slowly evaporated.\",Single-crystal X-ray diffraction,The frames were recorded using Bruker SMART BREEZE diffractometer on graphite-monochromated Mo-Kα radiation (λ 0.71073 Å) and a 1 K charge-coupled device (CCD) area detector at room temperature.\r\n10.1021/acsomega.8b02877,tetrakis((S)-1-phenylethylammonium) bismuth bromide,C32H48N4Bi2Br10,\"(S)-(MBA)4[BiBr10], (S)-1-phenylethylammonium bromobismuthate(III), [((S)-C8H12N)4][Bi2Br10]\",C8H12N,\"Bi2Br10, Bismuth bromide\",tetrakis((S)-1-phenylethylammonium) bismuth bromide,0,single crystal,,,,,,,,\"(S)-(−)-1-phenylethylamine ((S)-1-PEA, >99%), N,N′-dimethylformamide (DMF, anhydrous, 99.9%), bismuth-(III) bromide (BiBr3, 99.9%), and hydrobromic acid (HBr, 48 wt %)\",Yellow large plate-like crystals,\"[((S)-C8H12N)4]-[Bi2Br10][(S)-1] was grown through a slow evaporation method. BiBr3 (0.8 x 10^{−3} mol, 0.359 g) and (S)-1- phenylethylamine (1.6 x 10^{−3} mol, 0.206 mL) were dissolved in 6 mL of a 48% HBr aqueous solution. The solution mixture was heated at 60 °C for 20 min and slowly cooled to room temperature. Yellow crystals of compounds (S)-1 were grown in 2 days as the solvent slowly evaporated.\",Single-crystal X-ray diffraction,\"Frames were collected using ADSC Quantum-210 CCD diffractometer with synchrotron radiation (λ = 0.63000 Å) at two-dimensional supramolecular crystallography at the Pohang Accelerator Laboratory, Korea.\"\r\n10.1021/acsphotonics.8b00052,Bis(cyclohexylammonium) cadmium bromide,C12H28N2CdBr4,\"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",C6H14N,\"CdBr4, Cadmium bromide\",bis(cyclohexylammonium) cadmium bromide,2,single crystal,,,,,,,,\"cyclohexylamine, HBr, CdBr2\",Colorless millimeter-sized plate-like crystal,\"Step 1: synthesis of cyclohexylammonium salt C6H11NH2·HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20°C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. Step 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days.\",Single crystals X-ray diffraction,\"Diffractometer is Oxford Diffraction, equipped with two dimensional ATLAS detector. Graphite monochromatized Mo Kα radiation (λ = 0.71073 Å) was used. Unit cell determination and data reduction was performed by CRYSALIS program suite51 on the full set of data. Crystal structure resolution was obtained using \r\nSHELXS software by direct method.\"\r\n10.1021/acsphotonics.8b00052,Bis(cyclohexylammonium) cadmium bromide,C12H28N2CdBr4,\"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",C6H14N,\"CdBr4, Cadmium bromide\",bis(cyclohexylammonium) cadmium bromide,2,single crystal,,,,,,,,\"cyclohexylamine, HBr, CdBr2\",Colorless millimeter-sized plate-like crystal,\"Step 1: synthesis of cyclohexylammonium salt C6H11NH2·HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20°C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. \r\nStep 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days.\",Double monochromator with photomultiplier.,A double monochromator U1000 equipped with a photomultiplier was used. The excitation wavelength was 325 nm (3.815 eV).\r\n10.1021/acsphotonics.8b00052,Bis(cyclohexylammonium) cadmium bromide,C12H28N2CdBr4,\"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",C6H14N,\"CdBr4, Cadmium bromide\",bis(cyclohexylammonium) cadmium bromide,2,film,,,,,,,,\"cyclohexylamine, HBr, CdBr2, N,N-dimethylformamide solvent (DMF)\",200 nm thick (C6H11NH3)2CdBr4 film,\"Step 1: synthesis of cyclohexylammonium salt C6H11NH2·HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20°C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. \r\nStep 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days.\r\nStep 3: 10mg single crystal (C6H11NH3)2CdBr4 was dissolved in 1 mL of DMF.  10 μL of the above solution was spin-coated on a clean glass at 1500 rpm for 30s, The obtained film was then annealed in air at 80 °C for 5 min to remove residual solvent.\",UV-vis absorption (transmission mode),Adsorption spectra was measured by PerkinElmer (Lambda 950) spectrophotometer.  A coldfinger of a helium closed cycle cryostat was used to control the temperature of the samples.\r\n10.1021/acsphotonics.8b00052,Bis(cyclohexylammonium) cadmium bromide,C12H28N2CdBr4,\"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",C6H14N,\"CdBr4, Cadmium bromide\",bis(cyclohexylammonium) cadmium bromide,2,film,,,,,,,,\"cyclohexylamine, HBr, CdBr2, N,N-dimethylformamide solvent (DMF)\",200 nm thick (C6H11NH3)2CdBr4 film,\"Step 1: synthesis of cyclohexylammonium salt C6H11NH2·HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20°C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. Step 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days. Step 3: 10mg single crystal (C6H11NH3)2CdBr4 was dissolved in 1 mL of DMF. 10 μL of the above solution was spin-coated on a clean glass at 1500 rpm for 30s, The obtained film was then annealed in air at 80 °C for 5 min to remove residual solvent.\",UV-vis absorption (transmission mode),Adsorption spectra was measured by PerkinElmer (Lambda 950) spectrophotometer.  A coldfinger of a helium closed cycle cryostat was used to control the temperature of the samples.\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,single crystal,,,,,,,,\"Pb(NO3)2, KBr, HBr (48% aqueous), CsBr, ethanol (EtOH)\",\"orange, transparent crystals\",\"PbBr2 was first synthesized by dissolving Pb(NO3)2 (0.15 mol, 49.6 g) in 100 mL of boiling H2O. Meanwhile, KBr (0.3 mol, 35.7 g) was dissolved in 50 mL of H2O in a separate beaker and then slowly added to the Pb(NO3)2 solution with constant stirring. As a result, PbBr2 immediately precipitated and after 15 minutes of stirring, the solution was cooled to room temperature. The PbBr2 was filtered under vacuum, washed with distilled water, and dried overnight. This product was used in the synthesis of CsPbBr3. The PbBr2 (20 mmol, 7.31 g) was dissolved in 30 mL of HBr (48% wt.). A pale, yellow solution resulted, and CsBr (20 mmol, 4.26 mg) was dissolved in 10 mL of H2O. A bright orange solid immediately precipitated. The solid was suction filtered, washed with EtOH, dried under vacuum. Finally, the Bridgeman Method was performed to obtain single crystals. 6g of CsPbBr3 were ground with mortar and pestle, placed in a silica tub (OD/ID: 9mm/7mm), and the tube compilation was brought to a 10^{-4} mbar vacuum and flame-sealed. Then, the ampoule was attached to a clock mechanism, lowered into a 3-zone vertical tube furnace (temperature gradient: 10º C/mm). Dropping speed varied from 3 to 30 mm/h.\",Single Crystal X-ray diffraction,\"STOE IPDS II or IPDS 2T diffractometer were used. Mo Kα radiation (λ= 0.71073 Å) was performed, and diffractometers were operating at 50 kV and 40 mA. Absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs. Structures were solved directly and refined by full matrix least squares on F2 with the SHELXTL program package. Rotax functions of PLATON software (in WINGX platform) were used to find correct space group.\"\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,single crystal,,,,,,,,\"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH),\",Orange transparent crystals,\"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. \r\n6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",UV-vis absorbance,\"The spectrum was recorded using a Shimadzu UV-3101 PC double-beam, double monochromator spectrophotometer. Tauc plot with direct band gap assumption was used to obtain the band gap.\"\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,single crystal,,,,,,,,\"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",Orange transparent crystals,\"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. 6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",Photoluminescence,\"Low temperature PL measurements were performed on polished, etched samples. Excitation source was He-Cd (325 nm) or N2 (337nm) laser. Spectrum was analyzed with 0.75-m SPEX grating monochromator. Signal was detected with R928 Hamamatsu photomultiplier tube (PMT) and phase sensitive detection lock-in system.\"\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,single crystal,,,,,,,,\"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",Orange transparent crystals,\"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. 6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",Raman spectroscopy,DeltaNu Advantage NIR spectrometer was used with 785 nm irradiation and a CCD camera detector with backscattered setup. Max power of 60 mW and beam diameter of 35 μm were used. Spectra was collected with integration times of 0.1-1 s.\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,single crystal,,,,,,,,\"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",Orange transparent crystals,\"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. 6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",Photoluminescence,\"Low temperature PL measurements were performed on polished, etched samples. Excitation source was He-Cd (325 nm) or N2 (337nm) laser. Spectrum was analyzed with 0.75-m SPEX grating monochromator. Signal was detected with R928 Hamamatsu photomultiplier tube (PMT) and phase sensitive detection lock-in system.\"\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,unknown,,,,,,,,,,,Photoluminescence,\"Low temperature PL measurements were performed on polished, etched samples. Excitation source was He-Cd (325 nm) or N2 (337nm) laser. Spectrum was analyzed with 0.75-m SPEX grating monochromator. Signal was detected with R928 Hamamatsu photomultiplier tube (PMT) and phase sensitive detection lock-in system.\"\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,single crystal,,,,,,,,,,,UV-vis absorbance,\"Optical diffuse-reflectance measurements were executed at 298 K with a Shimadzu UV-3101 PC double-beam, double monochromator spectrophotometer between 200 to 2500 nm. One Nicolet 6700 IR spectrometer with a diffuse-reflectance kit was used for 4000-400cm^{-1} region. The reflectance vs. wavelength data was used to convert the data to absorption data via the Kubelka-Munk equation: α/S = (1-R)^2/2R.\"\r\n10.1021/cg400645t,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,powder,,,,,,,,\"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",Orange powder,\"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum.\",UV-vis absorbance (diffuse reflectance),\"Optical diffuse-reflectance measurements were executed at 298 K with a Shimadzu UV-3101 PC double-beam, double monochromator spectrophotometer between 200 to 2500 nm. One Nicolet 6700 IR spectrometer with a diffuse-reflectance kit was used for 4000-400cm^{-1} region. The reflectance vs. wavelength data was used to convert the data to absorption data via the Kubelka-Munk equation: α/S = (1-R)^2/2R.\"\r\n10.1021/cm010105g,3-fluoro-2-phenethylammonium tin iodide,C16H22F2N2SnI4,\"3-fluoro-2-phenylethanaminium tetraiodostannate(II), (3-FPEA)2SnI4, (C8H11FN)2(I4Sn)\",C8H11FN,\"SnI4, Tin iodide\",3-fluoro-2-phenylethanaminium tin (II) iodide,2,single crystal,,,,,,,,\"SnI2 (Aldrich, anhydrous beads, 99.999%), anhydrous 2-butanol, 3-fluorophenethylamine (Aldrich, 99%), HI (57wt%)\",\"dark red, thin (3- FPEA)2SnI4 crystals\",\"In an inert environment, 1.118 g (3 mmol) of SnI2 was added to 6 mL of anhydrous 2-butanol in a test tube. Further, 0.78 mL (0.835 g; 6 mmol) of 3-fluorophenethylamine was added.The mixture was cooled to -5 °C and 1 mL of HI was added. The mixture was heated to 94 °C. After the complete dissolution of SnI2, the solution was cooled at 3 °C/h to 0 °C.\",single-crystal X-ray diffraction,Bruker SMART CCD diffractometer with a normal focus 2.4 kW sealed tube X-ray source (MoKα radiation; λ = 0.71073 Å)\r\n10.1021/cm010105g,4-fluoro-2-phenethylammonium tin iodide,C16H22F2N2SnI4,\"4-fluoro-2-phenylethanaminium tetraiodostannate(II), (4-FPEA)2SnI4, (C8H11FN)2(I4Sn)\",C8H11FN,\"SnI4, Tin iodide\",4-fluoro-2-phenylethanaminium tin (II) iodide,2,single crystal,,,,,,,,\"SnI2 (Aldrich, anhydrous beads, 99.999%), anhydrous 2-butanol, 4-fluorophenethylamine (Aldrich, 99%), HI (57wt%)\",\"dark red, thin (4- FPEA)2SnI4 crystals\",\"In an inert environment, 1.118 g (3 mmol) of SnI2 was added to 10 mL of anhydrous 2-butanol in a test tube. Further, 0.79 mL (0.835 g; 6 mmol) of 4-fluorophenethylamine was added.The mixture was cooled to -5 °C and 2 mL of HI was added. The mixture was heated to 94 °C. After complete dissolution of SnI2, the solution was cooled at 3 °C/h to 0 °C.\",Single crystal XRD,Bruker SMART CCD diffractometer with a normal focus 2.4 kW sealed tube X-ray source (MoKα radiation; λ = 0.71073 Å)\r\n10.1021/cm034267j,\"2,3,4,5,6-pentafluorophenethylammonium 2-naphthyleneethylammonium tin iodide\",C20H21N2F5SnI4,\"(5FPEA¬∑NEA)SnI4, 2,3,4,5,6-pentafluorophenethylammonium 2-naphthyleneethylammonium tetraiodostannate(II)\",C20H21N2F5,\"SnI4, Tin iodide\",\"2,3,4,5,6-pentafluorophenethylammonium 2-naphthyleneethylammonium tin iodide\",2,single crystal,,,,,,,,\"SnI2, F5C6CH2CH2NH3I, C11H12NI, C2H3N, C7H8O\",\"platelike, bright red crystals\",\"Growing the (5FPEA·NEA)SnI4 crystals through the slow evaporation of acetonitrile/anisole mixed solution dissolving the organic and inorganic salts. Adding 37.0 mg (0.10 mmol) of SnI2, 34 mg (0.10 mmol) of 2,3,4,5,6-pentafluorophenethylammonium iodide, and 30 mg (0.10 mmol) of 2-naphthyleneethylammonium iodide into a vial under an argon atmosphere. Then 2.0 mL of anhydrous acetonitrile is added to dissolve the mixture to form a yellow solution. Filtering the solution through a Teflon filter (pore size:  0.2 μm) and adding 2.0 mL of anhydrous anisole into the solution. The vial is loosely capped and placed for 3 days for the formation of platelike, bright red crystals (90 mg, yield 90%).\",single-crystal X-ray diffraction,\"Selecting a blocklike crystal under a microscope and attaching it to the end of a quartz fiber with 5 min epoxy. Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo Kα radiation), is utilized to collect a full sphere of data at room temperature. A detector distance of approximately 5.0 cm and collection in 2272 frames with increasing ω is applied for obtaining intensity data. Using Shelxl 97 to solve and refine the crystal structure.\"\r\n10.1021/cm060714u,N-(3-aminopropyl)imidazole lead bromide,(C3H4N2(CH2)3NH3)PbBr4,\"(API)PbBr4, N-(3-aminopropyl)imidazole lead bromide, N-(3-aminopropyl)imidazole tetrabromoplumbate(II)\",C6H13N2,\"PbBr4, Lead bromide\",N-(3-aminopropyl)imidazole lead (II) bromide,2,single crystal,,,,,,,,\"N-(3-aminopropyl)imidazole (API, 98%, Aldrich), PbBr2 (99.999%, Aldrich), HBr (≥40%, Beijing Chemical Industry Co., Ltd.)\",Single crystals,\"A solution of PbBr2, API, and HBr was heated to 70 degrees Celsius and then cooled at 3 degrees per hour until reaching room temperature. This was performed in a nitrogen atmosphere and the crystals precipitated upon cooling.\",Single-crystal X-ray diffraction,\"A Rigaku RAXIS-RAPID image plate diffractometer was used to measure SCXRD. The w-scan technique was employed, and Mo Kalpha radiation was used. The SHELXS-97 program was used to solve the structure and the SHELXL-97 program was used to refine it via the full-matrix least-squares techniques.\"\r\n10.1021/cm060714u,N-(3-aminopropyl)imidazole lead bromide,(C3H4N2(CH2)3NH3)PbBr4,\"(API)PbBr4, N-(3-aminopropyl)imidazole lead bromide, N-(3-aminopropyl)imidazole tetrabromoplumbate(II)\",C6H13N2,\"PbBr4, Lead bromide\",N-(3-aminopropyl)imidazole lead (II) bromide,2,film,,,,,,,,\"N-(3-aminopropyl)imidazole (API, 98%, Aldrich), PbBr2 (99.999%, Aldrich), HBr (≥40%, Beijing Chemical Industry Co., Ltd.), DMF\",Thin film on quartz substrate,\"A solution of PbBr2, API, and HBr was heated to 70 degrees Celsius and then cooled at 3 degrees per hour until reaching room temperature. This was performed in a nitrogen atmosphere and the crystals precipitated upon cooling. Thin films were prepared via spin-coating. The crystals were dissolved into a DMF solution that was spin-coated onto a quartz substrate. The spinning cycle parameters were a spin rate of 1500 for 50 seconds and was followed by annealing the sample at 100 degrees Celsius for 20 minutes.\",Photoluminescence Excitation Spectroscopy,A Hitachi F-4500 spectrofluorimeter using a 150 W xenon lamp was used to measure the photoluminescence excitation and emission spectra.\r\n10.1021/cm060714u,N-(3-aminopropyl)imidazole lead bromide,(C3H4N2(CH2)3NH3)PbBr4,\"(API)PbBr4, N-(3-aminopropyl)imidazole lead bromide, N-(3-aminopropyl)imidazole tetrabromoplumbate(II)\",C6H13N2,\"PbBr4, Lead bromide\",N-(3-aminopropyl)imidazole lead (II) bromide,2,film,,,,,,,,\"N-(3-aminopropyl)imidazole (API, 98%, Aldrich), PbBr2 (99.999%, Aldrich), HBr (≥40%, Beijing Chemical Industry Co., Ltd.), DMF\",Thin film on quartz substrate,\"A solution of PbBr2, API, and HBr was heated to 70 degrees Celsius and then cooled at 3 degrees per hour until reaching room temperature. This was performed in a nitrogen atmosphere and the crystals precipitated upon cooling. Thin films were prepared via spin-coating. The crystals were dissolved into a DMF solution that was spin-coated onto a quartz substrate. The spinning cycle parameters were a spin rate of 1500 for 50 seconds and was followed by annealing the sample at 100 degrees Celsius for 20 minutes.\",Photoluminescence Excitation Spectroscopy,A Hitachi F-4500 spectrofluorimeter using a 150 W xenon lamp was used to measure the photoluminescence excitation and emission spectra. Excitation wavelength of 360 nm was used for the emission spectra.\r\n10.1021/cm062380e,Bis(2-chloroethylammonium) lead iodide,(Cl(CH2)2NH3)2PbI4,\"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",C2H7NCl,\"PbI4, Lead iodide\",bis(2-chloroethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",Red plate-like crystals,\"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",Single-crystal X-ray diffraction,A Bruker-Nonius KAPPA-CDD diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. The Shelxl97 package was used to both solve and refine the structures.\r\n10.1021/cm062380e,Bis(2-bromoethylammonium) lead iodide,C4H14N2Br2PbI4,\"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",C2H7NBr,\"PbI4, Lead iodide\",bis(2-bromoethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",Red plate-like crystals,\"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",Single-crystal X-ray diffraction,A Bruker-Nonius KAPPA-CDD diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. The Shelxl97 package was used to both solve and refine the structures.\r\n10.1021/cm062380e,Bis(2-iodoethylammonium) lead iodide,C4H14N2PbI6,\"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",C2H7NI,\"PbI4, Lead iodide\",bis(2-iodoethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Acetonitrile, HI, I(CH2)2NH2, PbI2\",Orange plate-like crystals,\"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",Single-crystal X-ray diffraction,A Bruker-Nonius KAPPA-CDD diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. The Shelxl97 package was used to both solve and refine the structures.\r\n10.1021/cm062380e,Bis(2-chloroethylammonium) lead iodide,(Cl(CH2)2NH3)2PbI4,\"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",C2H7NCl,\"PbI4, Lead iodide\",bis(2-chloroethylaminium) lead (II) iodide,2,film,,,,,,,,\"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",Thin film on glass substrate,\"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",UV-vis absorption,A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\r\n10.1021/cm062380e,Bis(2-chloroethylammonium) lead iodide,(Cl(CH2)2NH3)2PbI4,\"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",C2H7NCl,\"PbI4, Lead iodide\",bis(2-chloroethylaminium) lead (II) iodide,2,film,,,,,,,,\"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",Thin film on glass substrate,\"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",UV-vis absorption,A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\r\n10.1021/cm062380e,Bis(2-bromoethylammonium) lead iodide,C4H14N2Br2PbI4,\"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",C2H7NBr,\"PbI4, Lead iodide\",bis(2-bromoethylaminium) lead (II) iodide,2,film,,,,,,,,\"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",Thin film on glass substrate,\"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",UV-vis absorption,A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\r\n10.1021/cm062380e,Bis(2-bromoethylammonium) lead iodide,C4H14N2Br2PbI4,\"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",C2H7NBr,\"PbI4, Lead iodide\",bis(2-bromoethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",Thin film on glass substrate,\"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",UV-vis absorption,A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\r\n10.1021/cm062380e,Bis(2-iodoethylammonium) lead iodide,C4H14N2PbI6,\"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",C2H7NI,\"PbI4, Lead iodide\",bis(2-iodoethylaminium) lead (II) iodide,2,powder,,,,,,,,\"Acetonitrile, HI, I(CH2)2NH2, PbI2\",Orange plate-like crystals,\"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",UV-vis absorption,A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\r\n10.1021/cm062380e,Bis(2-iodoethylammonium) lead iodide,C4H14N2PbI6,\"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",C2H7NI,\"PbI4, Lead iodide\",bis(2-iodoethylaminium) lead (II) iodide,2,powder,,,,,,,,\"Acetonitrile, HI, I(CH2)2NH2, PbI2\",Orange plate-like crystals,\"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",UV-vis absorption,A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\r\n10.1021/cm062380e,Bis(2-chloroethylammonium) lead iodide,(Cl(CH2)2NH3)2PbI4,\"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",C2H7NCl,\"PbI4, Lead iodide\",bis(2-chloroethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",Red plate-like crystals,\"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",Thermogravimetric Analysis (TGA),A TGA-2050 Instruments System was used to perform the dynamic thermogravimetric analysis measurements under a nitrogen atmosphere. The temperature was increased at 10 degrees Celsius per minute over the range 25 to 900 degrees Celsius.\r\n10.1021/cm062380e,Bis(2-bromoethylammonium) lead iodide,C4H14N2Br2PbI4,\"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",C2H7NBr,\"PbI4, Lead iodide\",bis(2-bromoethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",Red plate-like crystals,\"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",Thermogravimetric Analysis (TGA),A TGA-2050 Instruments System was used to perform the dynamic thermogravimetric analysis measurements under a nitrogen atmosphere. The temperature was increased at 10 degrees Celsius per minute over the range 25 to 900 degrees Celsius.\r\n10.1021/cm062380e,Bis(2-iodoethylammonium) lead iodide,C4H14N2PbI6,\"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",C2H7NI,\"PbI4, Lead iodide\",bis(2-iodoethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Acetonitrile, HI, I(CH2)2NH2, PbI2\",Orange plate-like crystals,\"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",Thermogravimetric Analysis (TGA),A TGA-2050 Instruments System was used to perform the dynamic thermogravimetric analysis measurements under a nitrogen atmosphere. The temperature was increased at 10 degrees Celsius per minute over the range 25 to 900 degrees Celsius.\r\n10.1021/cm062380e,Bis(2-chloroethylammonium) lead iodide,(Cl(CH2)2NH3)2PbI4,\"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",C2H7NCl,\"PbI4, Lead iodide\",bis(2-chloroethylaminium) lead (II) iodide,2,single crystal,\"VASP Package, WIEN2K Package\",\"DFT, FLAPW method\",PBE96,6x6x4,,PAW,,,,,,\r\n10.1021/cm062380e,Bis(2-iodoethylammonium) lead iodide,C4H14N2PbI6,\"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",C2H7NI,\"PbI4, Lead iodide\",bis(2-iodoethylaminium) lead (II) iodide,2,single crystal,\"VASP Package, WIEN2K Package\",\"DFT, FLAPW method\",PBE96,8x4x2,,PAW,,,,,,\r\n10.1021/cm702405c,butylammonium tin iodide,C8H22N2SnI6,\"bis(butane-1-aminium) hexaiodostannate(II), BA2SnI4\",C4H11N,\"SnI6, Tin iodide\",bis(butane-1-aminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, Ethanol, SnI2, butylammonium iodide (BAI)\",dark purple plate-like crystals,\"In an inert atmosphere,  stoichiometric quantities of BAI and SnI2 were added to HI. The solution was heated to 75°C to dissolve the solids and subsequently cooled to 5 °C at a rate of 1.5 °C/hour.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ =  0.71069 Å).\r\n10.1021/cm702405c,Bis(butylammonium) tin iodide,(CH3(CH2)3NH3)2SnI4,\"(BA)2SnI4, (C4)2SnI4, bis(butylaminium) tetraiodostannate(II)\",C8H24N2,\"SnI4, Tin iodide\",bis(butylaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, Ethanol, SnI2, butylammonium iodide (BAI)\",dark purple plate-like crystals,\"In an inert atmosphere, stoichiometric quantities of BAI and SnI2 were added to HI. The solution was heated to 75°C to dissolve the solids and subsequently cooled to 5 °C at a rate of 1.5 °C/hour.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,Pentyldiammonium tin iodide,NH3(CH2)5NH3SnI4,\"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",C5H16N2,\"SnI4, Tin iodide\",pentyldiaminium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Black plate-like crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Dark plate-like crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,Bis((4-carboxycyclohexyl)methanaminium) tin iodide,\"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",(TRA)2 tetraiodostannate(II),C16H32N2O4,\"SnI4, Tin iodide\",Bis((4-carboxycyclohexyl)methanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Brown plate-like crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,Bis(iodobutylammonium) tin iodide,(I(CH2)4NH3)2SNI4,\"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",C8H22N2,\"SnI4, Tin iodide\",bis(iodobutylaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Red plate-like crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,Bis(4-aminobutyric acid) tin iodide,(HOOC(CH2)3NH3)2SnI4,\"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",C4NO2H10,\"SnI4, Tin iodide\",bis(4-aminiumbutanoic acid) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Brown plate-like crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,1-(aminoethyl)piperdinium tin iodide,(C5H10N)C2H4NH2,\"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",C7H16N2,\"SnI4, Tin iodide\",1-(aminoethyl)piperdinium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Red plate-like crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,3-iodopyridinium tin iodide,\"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",IC5H5N,\"SnI4, Tin iodide\",3-iodopyridinium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Brown plate-like crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Single-crystal X-ray diffraction,Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71069 Å).\r\n10.1021/cm702405c,Bis(butylammonium) tin iodide,(CH3(CH2)3NH3)2SnI4,\"(BA)2SnI4, (C4)2SnI4, bis(butylaminium) tetraiodostannate(II)\",C8H24N2,\"SnI4, Tin iodide\",bis(butylaminium) tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,Pentyldiammonium tin iodide,NH3(CH2)5NH3SnI4,\"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",C5H16N2,\"SnI4, Tin iodide\",pentyldiaminium tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,Bis((4-carboxycyclohexyl)methanaminium) tin iodide,\"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",(TRA)2 tetraiodostannate(II),C16H32N2O4,\"SnI4, Tin iodide\",Bis((4-carboxycyclohexyl)methanaminium) tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,Bis(iodobutylammonium) tin iodide,(I(CH2)4NH3)2SNI4,\"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",C8H22N2,\"SnI4, Tin iodide\",bis(iodobutylaminium) tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,Bis(4-aminobutyric acid) tin iodide,(HOOC(CH2)3NH3)2SnI4,\"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",C4NO2H10,\"SnI4, Tin iodide\",bis(4-aminiumbutanoic acid) tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,1-(aminoethyl)piperdinium tin iodide,(C5H10N)C2H4NH2,\"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",C7H16N2,\"SnI4, Tin iodide\",1-(aminoethyl)piperdinium tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,3-iodopyridinium tin iodide,\"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",IC5H5N,\"SnI4, Tin iodide\",3-iodopyridinium tin iodide,2,single crystal,CAESER Software Suite,Semiempirical model: Extended Huckel Method,,,,,,,,,,\r\n10.1021/cm702405c,Bis(butylammonium) tin iodide,(CH3(CH2)3NH3)2SnI4,\"(BA)2SnI4, (C4)2SnI4, bis(butylaminium) tetraiodostannate(II)\",C8H24N2,\"SnI4, Tin iodide\",bis(butylaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,Pentyldiammonium tin iodide,NH3(CH2)5NH3SnI4,\"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",C5H16N2,\"SnI4, Tin iodide\",pentyldiaminium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe method,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe method,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,Bis((4-carboxycyclohexyl)methanaminium) tin iodide,\"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",(TRA)2 tetraiodostannate(II),C16H32N2O4,\"SnI4, Tin iodide\",Bis((4-carboxycyclohexyl)methanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe method,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,Bis(iodobutylammonium) tin iodide,(I(CH2)4NH3)2SNI4,\"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",C8H22N2,\"SnI4, Tin iodide\",bis(iodobutylaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe method,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,Bis(4-aminobutyric acid) tin iodide,(HOOC(CH2)3NH3)2SnI4,\"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",C4NO2H10,\"SnI4, Tin iodide\",bis(4-aminiumbutanoic acid) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe method,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,1-(aminoethyl)piperdinium tin iodide,(C5H10N)C2H4NH2,\"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",C7H16N2,\"SnI4, Tin iodide\",1-(aminoethyl)piperdinium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe method,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,3-iodopyridinium tin iodide,\"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",IC5H5N,\"SnI4, Tin iodide\",3-iodopyridinium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe method,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\"\r\n10.1021/cm702405c,Pentyldiammonium tin iodide,NH3(CH2)5NH3SnI4,\"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",C5H16N2,\"SnI4, Tin iodide\",pentyldiaminium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. \r\n\r\nValues extracted from fitting equation 1 in the article to the resistivity data.\"\r\n10.1021/cm702405c,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\"\r\n10.1021/cm702405c,Bis((4-carboxycyclohexyl)methanaminium) tin iodide,\"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",(TRA)2 tetraiodostannate(II),C16H32N2O4,\"SnI4, Tin iodide\",Bis((4-carboxycyclohexyl)methanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\"\r\n10.1021/cm702405c,Bis(iodobutylammonium) tin iodide,(I(CH2)4NH3)2SNI4,\"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",C8H22N2,\"SnI4, Tin iodide\",bis(iodobutylaminium) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\"\r\n10.1021/cm702405c,Bis(4-aminobutyric acid) tin iodide,(HOOC(CH2)3NH3)2SnI4,\"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",C4NO2H10,\"SnI4, Tin iodide\",bis(4-aminiumbutanoic acid) tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\"\r\n10.1021/cm702405c,1-(aminoethyl)piperdinium tin iodide,(C5H10N)C2H4NH2,\"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",C7H16N2,\"SnI4, Tin iodide\",1-(aminoethyl)piperdinium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\"\r\n10.1021/cm702405c,3-iodopyridinium tin iodide,\"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",IC5H5N,\"SnI4, Tin iodide\",3-iodopyridinium tin iodide,2,single crystal,,,,,,,,\"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",Single crystals,\"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",Four-probe DC conductivity,\"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\"\r\n10.1021/cm9505097,Bis(Butylammonium) germanium iodide,C8H24N2GeI4,\"bis(butane-1-aminium) tetraiodogermanate(II), (C4H9NH3)2GeI4, (C4H12N)2GeI4\",C4H12N,\"GeI4, Germanium iodide\",bis(butane-1-aminium) germanium(II) iodide,2,single crystal,,,,,,,,\"GeI4, HI, H3PO2, C4H9NH2\",Bright orange sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.709 g (1.22 mmol) of GeI4 in 50 mL 3 M HI solution at 80 °C. Raise the temperature of the solution to 98 °C and add 4 mL concentrated (50 wt %) aqueous H3PO2 solution. Allow the reduction of GeI4 to GeI2 to proceed for approximately 4 h, then add a solution of 0.491 g (2.44 mmol) of (C4H9NH2).HI in 3 mL of concentrated (57 wt %) aqueous HI, producing a yellow solution. Allow the resulting solution to sit at 80 °C in flowing argon until approximately 50% of the solution had evaporated and then slowly (2-5 °C/h) cool to -10 °C. Filter out the crystals under flowing argon and dry in argon at 80 °C.\",Photoluminescence,\"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\"\r\n10.1021/cm9505097,Bis(Butylammonium) tin iodide,C8H24N2SnI4,\"bis(butane-1-aminium) tetraiodostannate(II), (C4H9NH3)2SnI4, (C4H12N)2SnI4\",C4H12N,\"SnI4, Tin iodide\",bis(butane-1-aminium) tin(II) iodide,2,single crystal,,,,,,,,\"SnI2, HI, C4H9NH2\",Dark red sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.481 g (1.29 mmol) of SnI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 °C. In a separate tube, dissolve 2.58 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 °C/h from 90 to -10 °C, filter the crystals formed under argon or nitrogen and dry in argon at 80 °C.\",Photoluminescence,\"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\"\r\n10.1021/cm9505097,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, C4H9NH2\",Orange-yellow sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.534 g (1.16 mmol) of PbI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 °C. In a separate tube, dissolve 2.32 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 °C/h from 90 to -10 °C, filter the crystals formed under argon or nitrogen and dry in argon at 80 °C.\",Photoluminescence,\"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\"\r\n10.1021/cm9505097,Bis(Butylammonium) germanium iodide,C8H24N2GeI4,\"bis(butane-1-aminium) tetraiodogermanate(II), (C4H9NH3)2GeI4, (C4H12N)2GeI4\",C4H12N,\"GeI4, Germanium iodide\",bis(butane-1-aminium) germanium(II) iodide,2,single crystal,,,,,,,,\"GeI4, HI, H3PO2, C4H9NH2\",Bright orange sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.709 g (1.22 mmol) of GeI4 in 50 mL 3 M HI solution at 80 °C. Raise temperature of the solution to 98 °C and add 4 mL concentrated (50 wt %) aqueous H3PO2 solution. Allow the reduction of GeI4 to GeI2 to proceed for approximately 4 h, then add a solution of 0.491 g (2.44 mmol) of (C4H9NH2).HI in 3 mL of concentrated (57 wt %) aqueous HI, producing a yellow solution. Allow the resulting solution to sit at 80 °C in flowing argon until approximately 50% of the solution had evaporated and then slowly (2-5 °C/h) cool to -10 °C. Filter out the crystals under flowing argon and dry in argon at 80 °C.\",Single crystal X-ray diffraction,\r\n10.1021/cm9505097,Bis(Butylammonium) tin iodide,C8H24N2SnI4,\"bis(butane-1-aminium) tetraiodostannate(II), (C4H9NH3)2SnI4, (C4H12N)2SnI4\",C4H12N,\"SnI4, Tin iodide\",bis(butane-1-aminium) tin(II) iodide,2,single crystal,,,,,,,,\"SnI2, HI, C4H9NH2\",Dark red sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.481 g (1.29 mmol) of SnI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 °C. In a separate tube, dissolve 2.58 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 °C/h from 90 to -10 °C, filter the crystals formed under argon or nitrogen and dry in argon at 80 °C.\",Single crystal X-ray diffraction,Select suitable single crystals in an argon-filled drybox (<1 ppm O2 and H2O) under a microscope and seal in quartz capillaries. Collect data at room temperature on an Enraf-Nonius CAD4 diffractometer with graphite-monochromatized Mo Ka radiation. Obtain unitcell parameters and the crystal orientation matrix by a least-squares fit of 25 reflections with 18° < 2θ < 30°. Monitor intensity control reflections every 5000s during the data collection. Little to no degradation was observed for the compounds. Use the NRCVAX 386 PC version program for structural solution and refinement.\r\n10.1021/cm9505097,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, C4H9NH2\",Orange-yellow sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.534 g (1.16 mmol) of PbI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 °C. In a separate tube, dissolve 2.32 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 °C/h from 90 to -10 °C, filter the crystals formed under argon or nitrogen and dry in argon at 80 °C.\",Single crystal X-ray diffraction,Select suitable single crystals in an argon-filled drybox (<1 ppm O2 and H2O) under a microscope and seal in quartz capillaries. Collect data at room temperature on an Enraf-Nonius CAD4 diffractometer with graphite-monochromatized Mo Ka radiation. Obtain unitcell parameters and the crystal orientation matrix by a least-squares fit of 25 reflections with 18° < 2θ < 30°. Monitor intensity control reflections every 5000s during the data collection. Little to no degradation was observed for the compounds. Use the NRCVAX 386 PC version program for structural solution and refinement.\r\n10.1021/cm9505097,Bis(Butylammonium) germanium iodide,C8H24N2GeI4,\"bis(butane-1-aminium) tetraiodogermanate(II), (C4H9NH3)2GeI4, (C4H12N)2GeI4\",C4H12N,\"GeI4, Germanium iodide\",bis(butane-1-aminium) germanium(II) iodide,2,single crystal,,,,,,,,\"GeI4, HI, H3PO2, C4H9NH2\",Bright orange sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.709 g (1.22 mmol) of GeI4 in 50 mL 3 M HI solution at 80 °C. Raise the temperature of the solution to 98 °C and add 4 mL concentrated (50 wt %) aqueous H3PO2 solution. Allow the reduction of GeI4 to GeI2 to proceed for approximately 4 h, then add a solution of 0.491 g (2.44 mmol) of (C4H9NH2).HI in 3 mL of concentrated (57 wt %) aqueous HI, producing a yellow solution. Allow the resulting solution to sit at 80 °C in flowing argon until approximately 50% of the solution had evaporated and then slowly (2-5 °C/h) cool to -10 °C. Filter out the crystals under flowing argon and dry in argon at 80 °C.\",Photoluminescence,\"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\"\r\n10.1021/cm9505097,Bis(Butylammonium) tin iodide,C8H24N2SnI4,\"bis(butane-1-aminium) tetraiodostannate(II), (C4H9NH3)2SnI4, (C4H12N)2SnI4\",C4H12N,\"SnI4, Tin iodide\",bis(butane-1-aminium) tin(II) iodide,2,single crystal,,,,,,,,\"SnI2, HI, C4H9NH2\",Dark red sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.481 g (1.29 mmol) of SnI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 °C. In a separate tube, dissolve 2.58 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 °C/h from 90 to -10 °C, filter the crystals formed under argon or nitrogen and dry in argon at 80 °C.\",Photoluminescence,\"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\"\r\n10.1021/cm9505097,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, C4H9NH2\",Orange-yellow sheetlike crystals,\"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\r\n\r\nDissolve 0.534 g (1.16 mmol) of PbI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 °C. In a separate tube, dissolve 2.32 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 °C/h from 90 to -10 °C, filter the crystals formed under argon or nitrogen and dry in argon at 80 °C.\",Photoluminescence,\"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\"\r\n10.1021/ic000794i,\"5,5‘ ‘‘-bis(aminoethyl)-2,2‘:5‘,2‘ ‘:5‘ ‘,2‘ ‘‘-quaterthiophene antimony iodide\",C20H22N2S4Sb(2/3)I4,\"5,5‘ ‘‘-bis(aminoethyl)-2,2‘:5‘,2‘ ‘:5‘ ‘,2‘ ‘‘-quaterthiophene tetraiodoantimonate(II), AE4TSb(2/3)I4, (AEQT)Sb(2/3)I4, AEQTSb(2/3)I4, (H2AEQT)Sb(2/3)I4, C20H22S4N2Sb(2/3)I4\",C20H22N2S4,\"Sb(2/3)I4, Antimony iodide\",\"5,5‘ ‘‘-bis(aminoethyl)-2,2‘:5‘,2‘ ‘:5‘ ‘,2‘ ‘‘-quaterthiophene antimony(II) iodide\",2,single crystal,,,,,,,,\"AEQT2HI (161.4 mg; 0.24 mmol), SbI3 salts (Aldrich, 99.999%, anhydrous), ethylene glycol (Aldrich, anhydrous, 99.8%), concentrated (57 wt %) aqueous HI (Aldrich, stabilized, 99.99%), 2-butanol (Aldrich, anhydrous, 99.5%)\",\"Dark red, sheetlike crystals\",\"Synthesize AEQT2HI from method described in [1].\r\n\r\nPurify the SbI3 salts (Aldrich, 99.999%, anhydrous) by sublimation. \r\n\r\nWeigh equimolar quantities of AEQT2HI (161.4 mg; 0.24 mmol) and SbI3 and add to a test tube under an inert atmosphere. Dissolve the contents at 112 °C in a solvent mixture of 36 mL of ethylene glycol and 0.6 mL of concentrated aqueous HI. Gradually add 18 mL of 2-butanol to form a small amount of red precipitate. Heat the mixture to 116 °C in a sealed tube to dissolve the mixture into a solution. Slow cool the solution at 1.5 °C/h to -20 °C to produce of dark red, sheetlike crystals of the (H2AEQT)Sb(2/3)I4 compound.\",Single-crystal X-ray diffraction,\"A very thin, sheetlike crystal, with the approximate dimensions \u00180.005 mm \u0002X 0.12 mm X\u0002 0.27 mm [<0.01 mm X\u0002 0.06 mm \u0002X 0.24 mm] was selected. Collect a full sphere of data at room temperature using a Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo-Ka radiation) 0.71073 Å.\"\r\n10.1021/ic000794i,\"5,5‘ ‘‘-bis(aminoethyl)-2,2‘:5‘,2‘ ‘:5‘ ‘,2‘ ‘‘-quaterthiophene bismuth iodide\",C20H22N2S4Bi(2/3)I4,\"5,5‘ ‘‘-bis(aminoethyl)-2,2‘:5‘,2‘ ‘:5‘ ‘,2‘ ‘‘-quaterthiophene tetraiodobismate(II), AE4TBi(2/3)I4, (AEQT)Bi(2/3)I4, AEQTBi(2/3)I4, (H2AEQT)Bi(2/3)I4, C20H22S4N2Bi(2/3)I4\",C20H22N2S4,\"Bi(2/3)I4, Bismuth iodide\",\"5,5‘ ‘‘-bis(aminoethyl)-2,2‘:5‘,2‘ ‘:5‘ ‘,2‘ ‘‘-quaterthiophene bismuth(II) iodide\",2,single crystal,,,,,,,,\"AEQT2HI (161.4 mg; 0.24 mmol), BiI3 salts (Aldrich, 99.999%, anhydrous), ethylene glycol (Aldrich, anhydrous, 99.8%), concentrated (57 wt %) aqueous HI (Aldrich, stabilized, 99.99%), 2-butanol (Aldrich, anhydrous, 99.5%)\",\"Dark red, sheetlike crystals\",\"Synthesize AEQT2HI from method described in [1].\r\n\r\nPurify the BiI3 salts (Aldrich, 99.999%, anhydrous) by sublimation. \r\n\r\nWeigh equimolar quantities of AEQT2HI (161.4 mg; 0.24 mmol) and BiI3 and add to a test tube under an inert atmosphere. Dissolve the contents at 112 °C in a solvent mixture of 36 mL of ethylene glycol and 0.6 mL of concentrated aqueous HI. Gradually add 18 mL of 2-butanol to form a small amount of red precipitate. Heat the mixture to 116 °C in a sealed tube to dissolve the mixture into a solution. Slow cool the solution at 1.5 °C/h to -20 °C to produce dark red, sheetlike crystals of the (H2AEQT)Bi(2/3)I4 compound.\",Single-crystal X-ray diffraction,\"A very thin, sheetlike crystal, with the approximate dimensions \u00180.005 mm \u0002X 0.12 mm X\u0002 0.27 mm [<0.01 mm X\u0002 0.06 mm \u0002X 0.24 mm] was selected. Collect a full sphere of data at room temperature using a Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo-Ka radiation) 0.71073 Å.\"\r\n10.1021/ic011190x,Hexaflourobenzene bis(phenethylammonium) tin iodide,C16H24N2SnI4:C6F6,\"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\"C8H12N, C6F6\",\"SnI4, Tin iodide\",hexafluorobenzene bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"Methanol, hexafluorobenzene, (PEA)2SnI4\",Red plate-like crystals,\"Crystals of (PEA)2SnI4 intercalated with hexafluorobenzene were prepared by mixing the base layered perovskite with methanol. Then an excess of hexafluorobenzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",Single-crystal X-ray diffraction,Data was collected with the Bruker SMART CCD diffractometer using 2.4 kW tube X-ray source (Mo Kα radiation).\r\n10.1021/ic011190x,Hexaflourobenzene bis(phenethylammonium) tin iodide,C16H24N2SnI4:C6F6,\"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\"C8H12N, C6F6\",\"SnI4, Tin iodide\",hexafluorobenzene bis(phenylethanaminium) tin iodide,2,film,,,,,,,,\"Methanol, hexafluorobenzene, (PEA)2SnI4\",Thin film on quartz substrate,Films of the intercalated layered perovskites were prepared by immersing the uninteracalated films in a benzene or hexafluorobenzene solution at room temperature for an hour. The films were encapsulated by thin polycarbonate sheet while still wet from their immersion. The encapsulation effectively laminates the hybrid film and provided a partial diffusion barrier for the intercalated species. XRD and optical measurements can be made through the polycarbonate sheet cover.,UV-vis Absorption,Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\r\n10.1021/ic011190x,Hexaflourobenzene bis(phenethylammonium) tin iodide,C16H24N2SnI4:C6F6,\"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\"C8H12N, C6F6\",\"SnI4, Tin iodide\",hexafluorobenzene bis(phenylethanaminium) tin iodide,2,film,,,,,,,,\"Methanol, hexafluorobenzene, (PEA)2SnI4\",Thin film on quartz substrate,Films of the intercalated layered perovskites were prepared by immersing the uninteracalated films in a benzene or hexafluorobenzene solution at room temperature for an hour. The films were encapsulated by thin polycarbonate sheet while still wet from their immersion. The encapsulation effectively laminates the hybrid film and provided a partial diffusion barrier for the intercalated species. XRD and optical measurements can be made through the polycarbonate sheet cover.,UV-vis Absorption,Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\r\n10.1021/ic011190x,Hexaflourobenzene bis(phenethylammonium) tin iodide,C16H24N2SnI4:C6F6,\"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\"C8H12N, C6F6\",\"SnI4, Tin iodide\",hexafluorobenzene bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"Methanol, hexafluorobenzene, (PEA)2SnI4\",Red plate-like crystals,\"Crystals of (PEA)2SnI4 intercalated with hexafluorobenzene were prepared by mixing the base layered perovskite with methanol. Then an excess of hexafluorobenzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",Thermogravimetric Analysis (TGA),TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\r\n10.1021/ic011190x,Hexaflourobenzene bis(phenethylammonium) tin iodide,C16H24N2SnI4:C6F6,\"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\"C8H12N, C6F6\",\"SnI4, Tin iodide\",hexafluorobenzene bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"Methanol, hexafluorobenzene, (PEA)2SnI4\",Red plate-like crystals,\"Crystals of (PEA)2SnI4 intercalated with hexafluorobenzene were prepared by mixing the base layered perovskite with methanol. Then an excess of hexafluorobenzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",Differential Scanning Calorimetry (DSC),DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\r\n10.1021/ic011190x,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,film,,,,,,,,\"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",Thin film on quartz substrate,\"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and also rectrystallized twice from a solution of methanol and toluene. \r\nTo produce films of the unintercalated systems, the recrystallized perovskites were dissolved in distilled methanol. Previously cleaned and prepared quartz substrates were used and the solution was spin coated onto them. The spinning cycle was 1 s ramp up to 1800 rpm, and then 30 s at 1800 rpm. Then the samples were annealed at 70 degrees Celsius for 15 minutes to remove any residual solvent.\",UV-vis absorption,Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\r\n10.1021/ic011190x,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,film,,,,,,,,\"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",Thin film on quartz substrate,\"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and also rectrystallized twice from a solution of methanol and toluene. To produce films of the unintercalated systems, the recrystallized perovskites were dissolved in distilled methanol. Previously cleaned and prepared quartz substrates were used and the solution was spin coated onto them. The spinning cycle was 1 s ramp up to 1800 rpm, and then 30 s at 1800 rpm. Then the samples were annealed at 70 degrees Celsius for 15 minutes to remove any residual solvent.\",UV-vis absorption,Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\r\n10.1021/ic011190x,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",Red plate-like crystals,\"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and recrystallized twice from a solution of methanol and toluene.\",Thermogravimetric Analysis (TGA),TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\r\n10.1021/ic011190x,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",Red plate-like crystals,\"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and also rectrystallized twice from a solution of methanol and toluene.\",Differential Scanning Calorimetry (DSC),DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\r\n10.1021/ic011190x,\"2,3,4,5,6-pentafluorophenethylammoniom tin iodide : Benzene\",C22H20N2F10SnI4,\"(2,3,4,5,6-FPEA)2SnI4¬∑(C6H6), (C6F5(CH2)2NH3)2SnI4¬∑(C6H6), benzene-intercalated 2,3,4,5,6-pentafluorophenethylammonium tin iodide, benzene 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\"C8H7NF5, C6H6\",\"SnI4, Tin iodide\",\"benzene 2,3,4,5,6-pentafluorophenethanaminium tin iodide\",2,single crystal,,,,,,,,\"Methanol, benzene, (C6F5C2H4NH3)2SnI4\",Red plate-like crystals,\"Crystals of (2,3,4,5,6-FPEA)2SnI4 intercalated with benzene were prepared by mixing the base layered perovskite with methanol. Then an excess of benzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",Single-crystal X-ray diffraction,Data was collected with the Bruker SMART CCD diffractometer using 2.4 kW tube X-ray source (Mo Kα radiation).\r\n10.1021/ic011190x,\"2,3,4,5,6-pentafluorophenethylammoniom tin iodide : Benzene\",C22H20N2F10SnI4,\"(2,3,4,5,6-FPEA)2SnI4¬∑(C6H6), (C6F5(CH2)2NH3)2SnI4¬∑(C6H6), benzene-intercalated 2,3,4,5,6-pentafluorophenethylammonium tin iodide, benzene 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\"C8H7NF5, C6H6\",\"SnI4, Tin iodide\",\"benzene 2,3,4,5,6-pentafluorophenethanaminium tin iodide\",2,single crystal,,,,,,,,\"Methanol, benzene, (C6F5C2H4NH3)2SnI4\",Red plate-like crystals,\"Crystals of (2,3,4,5,6-FPEA)2SnI4 intercalated with benzene were prepared by mixing the base layered perovskite with methanol. Then an excess of benzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",Thermogravimetric Analysis (TGA),TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\r\n10.1021/ic011190x,\"2,3,4,5,6-pentafluorophenethylammoniom tin iodide : Benzene\",C22H20N2F10SnI4,\"(2,3,4,5,6-FPEA)2SnI4¬∑(C6H6), (C6F5(CH2)2NH3)2SnI4¬∑(C6H6), benzene-intercalated 2,3,4,5,6-pentafluorophenethylammonium tin iodide, benzene 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\"C8H7NF5, C6H6\",\"SnI4, Tin iodide\",\"benzene 2,3,4,5,6-pentafluorophenethanaminium tin iodide\",2,single crystal,,,,,,,,\"Methanol, benzene, (C6F5C2H4NH3)2SnI4\",Red plate-like crystals,\"Crystals of (2,3,4,5,6-FPEA)2SnI4 intercalated with benzene were prepared by mixing the base layered perovskite with methanol. Then an excess of benzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",Differential Scanning Calorimetry (DSC),DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\r\n10.1021/ic011190x,\"2,3,4,5,6-pentafluorophenethylammoniom tin iodide\",C16H14N2F10SnI4,\"(2,3,4,5,6-FPEA)2SnI4, (C6F5(CH2)2NH3)2SnI4, 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",C8H7NF5,\"SnI4, Tin iodide\",\"2,3,4,5,6-pentafluorophenethanaminium tin iodide\",2,single crystal,,,,,,,,\"HI, SnI2, C6F5C2H4NH3I, toluene\",Red plate-like crystals,\"Crystals were grown by slowly cooling a solution of HI, C6F5C2H4NH3I, and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and recrystallized twice from a solution of methanol and toluene.\",Thermogravimetric Analysis (TGA),TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\r\n10.1021/ic011190x,\"2,3,4,5,6-pentafluorophenethylammoniom tin iodide\",C16H14N2F10SnI4,\"(2,3,4,5,6-FPEA)2SnI4, (C6F5(CH2)2NH3)2SnI4, 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",C8H7NF5,\"SnI4, Tin iodide\",\"2,3,4,5,6-pentafluorophenethanaminium tin iodide\",2,single crystal,,,,,,,,\"HI, SnI2, C6F5C2H4NH3I, toluene\",Red plate-like crystals,\"Crystals were grown by slowly cooling a solution of HI, C6F5C2H4NH3I, and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and recrystallized twice from a solution of methanol and toluene.\",Differential Scanning Calorimetry (DSC),DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\r\n10.1021/ic0261474,Bis(2-bromophenethyl)ammonium tin iodide,(2-BrC6H4C2H4NH3)2SnI4,\"(2-BrPEA)2SnI4, bis(2-bromophenethanaminium) tetraiodostannate(II)\",BrC6H4C2H4NH3,\"SnI4, Tin iodide\",bis(2-bromophenethanaminium) tin iodide,2,single crystal,,,,,,,,\"SnI2, 2-BrC6H4C2H4NH3I, CH3OH, C6H5CH3\",\"platelike, bright red crystals\",\"Growing the crystal through the slow evaporation of methanol/toluene mixed solution dissolving the organic and inorganic salts. Adding 45.5 mg (0.122 mmol) SnI2 and 80.0 mg (0.244 mmol) (2-bromophenethyl)ammonium iodide into a vial under an inert atmosphere. Then 1.0 mL of anhydrous methanol is added to dissolve the mixture to form a yellow solution. Filtering the solution through a Teflon filter (pore size:  0.2 μm) and adding 2.0 mL of anhydrous toluene into the solution. The vial is loosely capped and placed for 3 days for the formation of platelike, bright red crystals (120 mg, yield 95%) during the slow cooling process.\",single-crystal X-ray diffraction,\"Selecting a blocklike crystal under a microscope and attaching it to the end of a quartz fiber with 5 min epoxy. Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo Kα radiation), is utilized to collect a full sphere of data at room temperature. A detector distance of approximately 5.0 cm and collection in 2272 frames with increasing ω is applied for obtaining intensity data. Using Shelxl 97 to solve and refine the crystal structure.\"\r\n10.1021/ic0261474,Bis(2-chlorophenethyl)ammonium tin iodide,(2-ClC6H4C2H4NH3)2SnI4,\"(2-ClPEA)2SnI4, bis(2-chlorophenethanaminium) tetraiodostannate(II)\",ClC6H4C2H4NH3,\"SnI4, Tin iodide\",bis(2-chlorophenethanaminium) tin iodide,2,single crystal,,,,,,,,\"SnI2, 2-ClC6H4C2H4NH3I, CH3OH, C6H5CH3\",\"thin platelike, dark red crystals\",\"Growing the crystal through the slow evaporation of methanol/toluene mixed solution dissolving the organic and inorganic salts. Adding 52.3 mg (0.140 mmol) SnI2 and 80.0 mg (0.282 mmol) of (2-chlorophenethyl)ammonium iodide into a vial under an inert atmosphere. Then 1.5 mL of anhydrous methanol is added to dissolve the mixture to form a yellow solution. Filtering the solution through a Teflon filter (pore size:  0.2 μm) and adding 3.0 mL of anhydrous toluene into the solution. The vial is loosely capped and placed for 3 days for the formation of thin platelike, darker red crystals (120 mg, yield 95%) during the slow evaporation process.\",single-crystal X-ray diffraction,\"Selecting a blocklike crystal under a microscope and attaching it to the end of a quartz fiber with 5 min epoxy. Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo Kα radiation), is utilized to collect a full sphere of data at room temperature. A detector distance of approximately 5.0 cm and collection in 2272 frames with increasing ω is applied for obtaining intensity data. Using Shelxl 97 to solve and refine the crystal structure.\"\r\n10.1021/ic0261981,Trimethylammonioethylammonium tin iodide,C5H16N2SnI4,\"(TMAEA)SnI4, ((CH3)3NCH2CH2NH3)SnI4, Trimethylammonioethylammonium tetraiodostannate(II)\",C5H16N2,\"SnI4, Tin iodide\",\"N,N,N-trimethylethane-1,2-diaminium tin iodide\",2,single crystal,,,,,,,,\"Tin iodide, 2-trimethylammonioethylammonium diiodide, methanol, acetonitrile\",Black plate-like crystals,\"Tin(II) iodide and trimethylammonioethylammonium diiodide were combined with methanol and acetonitrile. After 2 hours of stirring the solution became yellow and transparent, and passed through a filter with pore sizes of 0.2 microns. The solvent was allowed to evaporate at room temperature for 2-3 days, leaving behind chunky, black crystals.\",Single-crystal X-ray diffraction,Single crystal XRD was performed at room temperature using a Bruker SMART CCD diffractometer. A normal focus 2.4 kW sealed tube X-ray source (Mo Kα radiation) was used. The crystal structure was solved by direct methods and refined on F2 using the SHELXL 97 package.\r\n10.1021/ic0261981,Trimethylammonioethylammonium tin iodide,C5H16N2SnI4,\"(TMAEA)SnI4, ((CH3)3NCH2CH2NH3)SnI4, Trimethylammonioethylammonium tetraiodostannate(II)\",C5H16N2,\"SnI4, Tin iodide\",\"N,N,N-trimethylethane-1,2-diaminium tin iodide\",2,film,,,,,,,,\"Tin iodide, 2-trimethylammonioethylammonium diiodide, methanol, acetonitrile, DMF\",Dark red thin films on glass,\"Tin(II) iodide and trimethylammonioethylammonium diiodide were combined with methanol and acetonitrile. After 2 hours of stirring the solution became yellow and transparent, and passed through a filter with pore sizes of 0.2 microns. The solvent was allowed to evaporate at room temperature for 2-3 days, leaving behind chunky, black crystals. To produce thin films, the crystals were first dissolved in DMF to produce a transparent and yellow solution. 3-4 drops of the solution were put on a glass plate and heated to 155 degrees Celsius. A small puddle of about one square centimeter formed and within a minute began depositing black solid around its circumference. A caption sheet was used to spread the remaining solution evenly over the glass slide. A dark red film was formed on the glass slide and was kept at 155 degrees Celsius for another 2 minutes. XRD confirmed the formation of the layered perovskite structure.\",UV-vis absorption,The UV-vis absorption spectrum was measured via absorption spectroscopy at room temperature.\r\n10.1021/ic0261981,Trimethylammonioethylammonium tin iodide,C5H16N2SnI4,\"(TMAEA)SnI4, ((CH3)3NCH2CH2NH3)SnI4, Trimethylammonioethylammonium tetraiodostannate(II)\",C5H16N2,\"SnI4, Tin iodide\",\"N,N,N-trimethylethane-1,2-diaminium tin iodide\",2,film,,,,,,,,\"Tin iodide, 2-trimethylammonioethylammonium diiodide, methanol, acetonitrile, DMF\",Dark red thin films on glass,\"Tin(II) iodide and trimethylammonioethylammonium diiodide were combined with methanol and acetonitrile. After 2 hours of stirring the solution became yellow and transparent, and passed through a filter with pore sizes of 0.2 microns. The solvent was allowed to evaporate at room temperature for 2-3 days, leaving behind chunky, black crystals. To produce thin films, the crystals were first dissolved in DMF to produce a transparent and yellow solution. 3-4 drops of the solution were put on a glass plate and heated to 155 degrees Celsius. A small puddle of about one square centimeter formed and within a minute began depositing black solid around its circumference. A caption sheet was used to spread the remaining solution evenly over the glass slide. A dark red film was formed on the glass slide and was kept at 155 degrees Celsius for another 2 minutes. XRD confirmed the formation of the layered perovskite structure.\",UV-vis absorption,The UV-vis absorption spectrum was measured via absorption spectroscopy at room temperature. The exact instrument is unknown.\r\n10.1021/ic034235y,\"5,5‘-bis(ammoniumethylsulfanyl)-2,2‘-bithiophene lead iodide\",C12H18N2S4PbI4,\"(2,2'-(thioethanaminium)-5,5'-bithiophene) tetraiodoplumbate(II), (BAESBT)PbI4\",C6H9I2N,\"PbI4, Lead iodide\",\"(2,2'-(thioethanaminium)-5,5'-bithiophene) lead (II) iodide\",2,single crystal,,,,,,,,\"(BAESBT)Cl2 , PbI2, KI, HI\",Orange plate single crystals,\"First prepare (BAESBT)Cl2 Salt (refer to the experimental section). Mix (BAESBT)Cl2 (12.8 mg, 0.03 mmol), PbI2 (15 mg, 0.033 mmol), excess KI (7 g), one drop of concentrated HI, and H2O (10 mL) in a sealed Pyrex tube. Keep the temperature at 90 °C for 1 h and then at 110 °C for 4 h. Subsequently, cool to room temperature at 2 °C/h resulting in well-formed orange plate single crystals.\",Single-crystal X-ray diffraction,\"Enraf-Nonius MACH3 four-circle diffractometer with graphite monochromated, Mo Kα radiation (λ = 0.71073 Å)\"\r\n10.1021/ic034235y,\"Tetrakis(5-ammoniumethylsulfanyl-2,2‘-bithiophene) lead iodide\",C40H48N4S12Pb3I10,\"(AESBT)4Pb3I10, tetrakis(2,2'-(thioethanaminium)-5,5'-bithiophene) decaiodo triplumbate(II)\",C10H12NS3,\"Pb3I10, Lead iodide\",\"tetrakis(2,2'-(thioethanaminium)-5,5'-bithiophene) lead iodide\",2,single crystal,,,,,,,,\"(AESBT)Cl, PbI2, HI\",Yellow needle single crystals,\"First prepare (AESBT)Cl Salt (refer to the experimental section). Mix (AESBT)Cl (9.7 mg, 0.037 mmol), PbI2 (12.8 mg, 0.028 mmol), three drops of concentrated HI, and H2O (4 mL) in a sealed Pyrex tube. Keep the temperature at 100 °C for 4 h and then cool to room temperature at 2 °C/h affording well-formed yellow needle single crystals.\",Single-crystal X-ray diffraction,\"Enraf-Nonius MACH3 four-circle diffractometer with graphite monochromated, Mo Kα radiation (λ = 0.71073 Å)\"\r\n10.1021/ic034235y,\"Tris(5-ammoniumethylsulfanyl-2,2‘-bithiophene) bismuth iodide\",C30H36N3S9Bi2I9,\"(AESBT)3Bi2I9, tris(2,2'-(thioethanaminium)-5,5'-bithiophene) nonaiodo dibismuthate(II)\",C10H12NS3,\"Bi2I9, Bismuth iodide\",\"tris(2,2'-(thioethanaminium)-5,5'-bithiophene) lead (II) iodide\",2,single crystal,,,,,,,,\"(AESBT)Cl, BiCl3, KI, HI\",Red plate single crystals,\"First prepare (AESBT)Cl Salt (refer to the experimental section). Mix (AESBT)Cl (16.7 mg, 0.06 mmol), BiCl3 (18.5 mg, 0.028 mmol), excess KI (1 g), two drops of concentrated HI and H2O (5 mL) in a sealed Pyrex tube. Keep the temperature at 100 °C for 10 h and then cool to room temperature at 2 °C/h leading to well-formed red plate single crystals.\",Single-crystal X-ray diffraction,\"STOE-IPDS diffractometer with graphite monochromated, Mo Kα radiation (λ = 0.71073 Å)\"\r\n10.1021/ic048814u,2-hydroxyethylammonium lead iodide,C4H16N2O2PbI4,\"bis(2-hydroxyethanaminium) tetraiodoplumbate(II), (HO(CH2)2NH3)2PbI4\",C2H8NO,\"PbI4, Lead iodide\",bis(2-hydroxyethanaminium) lead (II) iodide,2,single crystal,,,,,,,,\"ethanolamine (NH2(CH2)2OH), lead iodide (PbI2), Conc. HI, Acetonitrile (CH3CN)\",Orange needle-like crystal,\"NH2(CH2)2OH (111 mg, 1.82 mmol), PbI2 (420 mg, 0.91 mmol), a few drops of concentrated HI, and acetonitrile (20 mL) was stirred a few minutes at room temperature. Evaporating the solution at 20 °C by stirring formed the crystals. The crystals were filtered and washed with cold acetonitrile.\",Single crystal X-ray diffraction,Frames were collected on an Enraf-Nonius MACH3 four-circle diffractometer using graphite-monochromated Mo Kα radiation (λ= 0.710 73 Å).\r\n10.1021/ic048814u,2-hydroxyethylammonium lead iodide,C4H16N2O2PbI4,\"bis(2-hydroxyethanaminium) tetraiodoplumbate(II), (HO(CH2)2NH3)2PbI4\",C2H8NO,\"PbI4, Lead iodide\",bis(2-hydroxyethanaminium) lead (II) iodide,2,film,,,,,,,,\"ethanolamine (NH2(CH2)2OH), lead iodide (PbI2), Conc. HI, Acetonitrile (CH3CN)\",(HO(CH2)2NH3)2PbI4 film,\"NH2(CH2)2OH (111 mg, 1.82 mmol), PbI2 (420 mg, 0.91 mmol), a few drops of concentrated HI, and acetonitrile (20 mL) was stirred a few minutes at room temperature. Evaporating the solution at 20 °C by stirring formed the crystals. The crystals were filtered and washed with cold acetonitrile.\r\nThe crystals were further dissolved in acetonitrile and spin-coated to form the films.\",UV-visible absorption,Spectra were recorded using a Lambda 19 Perkin-Elmer spectrometer.\r\n10.1021/ic0498081,dimethylamine manganese formate,C2H8NMnC3H3O6,\"Mn(CHOO)3[NH2(CH3)2], [(CH3)2NH2][Mn(CHOO)3]\",C2H8N,\"[Mn(CHOO)3]-, Manganese formate\",\"N,N-dimethanaminium manganese formate\",3,single crystal,,,,,,,,\"MnCl2·4H2O, dimethylformamide (DMF),\",Colorless block-like crystals,\"MnCl2·4H2O(1 mmol), DMF (6 mL), and H2O (6 mL) were heated in a Teflon-lined autoclave at 140 °C for 3 days. The solution was slowly cooled and the residual solution was evaporated at room temperature for about 1 week.\",Single-crystal X-ray diffraction,Data were collected using Rigaku R-Axis RIPID IP with Mo−Kα radiation (λ = 0.71073 Å) at 293 K.\r\n10.1021/ic0498081,dimethylamine cobalt formate,C2H8NCoC3H3O6,\"Co(CHOO)3[NH2(CH3)2], [(CH3)2NH2][Co(CHOO)3]\",C2H8N,\"[Co(CHOO)3]-, Cobalt formate\",\"N,N-dimethanaminium cobalt formate\",3,single crystal,,,,,,,,\"CoCl2·6H2O, dimethylformamide (DMF),\",Pink block-like crystals,\"CoCl2·6H2O (1 mmol), DMF (6 mL), and H2O (6 mL) were heated in a Teflon-lined autoclave at 140 °C for 3 days. The solution was slowly cooled and the residual solution was evaporated at room temperature for about 1 week.\",Single-crystal X-ray diffraction,Data were collected using Rigaku R-Axis RIPID IP with Mo−Kα radiation (λ = 0.71073 Å) at 293 K.\r\n10.1021/ic0498081,dimethylamine nickle formate,C2H8NNiC3H3O6,\"Ni(CHOO)3[NH2(CH3)2], [(CH3)2NH2][Ni(CHOO)3]\",C2H8N,\"[Ni(CHOO)3]-, Nickle formate\",\"N,N-dimethanaminium nickle formate\",3,single crystal,,,,,,,,\"NiCl2·6H2O, dimethylformamide (DMF),\",Blue block-like crystals,\"NiCl2·6H2O (1 mmol), DMF (6 mL), and H2O (6 mL) were heated in a Teflon-lined autoclave at 140 °C for 3 days. The solution was slowly cooled and the residual solution was evaporated at room temperature for about 1 week.\",Single-crystal X-ray diffraction,Data were collected using Rigaku R-Axis RIPID IP with Mo−Kα radiation (λ = 0.71073 Å) at 293 K.\r\n10.1021/ic0521527,dimethylammonium iron azido formate,[(CH3)2NH2][Fe(N3)2(HCOO)],[Fe(N3)2(HCOO)][(CH3)2NH2],C2NH8,[Fe(N3)2(HCOO)]-,dimethylammonium iron azido formate,1,single crystal,,,,,,,,\"formic acid, NaN3, dimethylamine, Fe(ClO4)2‚4H2O, methanol\",Column shaped yellow-green crystals,\"In a methanol solution containing formic acid, NaN3, and dimethylamine, another methanol solution of Fe(ClO4)2‚4H2O was diffused.\",Single-crystal X-ray diffraction,Data were collected using a NONIUS KappaCCD Diffractometer with Mo Kα (λ = 0.71073 Å) radiation.\r\n10.1021/ic0521527,dimethylammonium cobalt azido formate,[(CH3)2NH2][Co(N3)2(HCOO)],[Co(N3)2(HCOO)][(CH3)2NH2],C2NH8,[Co(N3)2(HCOO)]-,dimethylammonium cobalt azido formate,1,single crystal,,,,,,,,\"formic acid, NaN3, dimethylamine, CoCl2‚6H2O, methanol\",Column shaped pink crystals,\"In a methanol solution containing formic acid, NaN3, and dimethylamine, another methanol solution of CoCl2‚6H2O was diffused.\",Single-crystal X-ray diffraction,Data were collected using a NONIUS KappaCCD Diffractometer with Mo Kα (λ = 0.71073 Å) radiation.\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of  formed.\",Single Crystal X-Ray Diffraction,A Rigaku Mercury CCD diffractometer was used. Mo Kα radiation was used with the ω scan technique at 123 Kelvin. The structure was solved by direct methods with the Siemens SHELXTL Version 5 package. Full-matrix least-squares refinement on F2 was used to refine the structure.\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,Semi-empirical model: Extended Huckel Theory (EHT),,,non-relativsitic,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",,\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",Diffuse Reflectance Spectra,\"The absorption spectrum was calculated from measured reflection spectrum. Diffuse reflection spectroscopy was measured with a PE Lambda 35 UV-vis spectrophotometer with an integrating sphere at 273 Kelvin, and BaSO4 was the reference. The Kubelka-Munk function was used to calculate the absorption spectrum, and direct extrapolation was used to find the band gap value.\"\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",Diffuse Reflectance Spectra,\"The absorption spectrum was calculated from measured reflection spectrum. Diffuse reflection spectroscopy was measured with a PE Lambda 35 UV-vis spectrophotometer with an integrating sphere at 273 Kelvin, and BaSO4 was the reference. The Kubelka-Munk function was used to calculate the absorption spectrum, and direct extrapolation was used to find the band gap value.\"\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",Photoluminescence Spectroscopy,PL and PL excitation spectra were measured using a JY Fluorlog-322 at room temperature. PL was measured with an excitation wavelength of 371 nm. PLE was measured at emission wavelengths of 440 and 501 nm.\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals formed.\",Photoluminescence Spectroscopy,PL and PL excitation spectra were measured using a JY Fluorlog-322 at room temperature. PL was measured with an excitation wavelength of 371 nm. PLE was measured at emission wavelengths of 440 and 501 nm.\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15, and after the two days and upon cooling, yellow crystals formed.\",Photoluminescence Spectroscopy,PL and PL excitation spectra were measured using a JY Fluorlog-322 at room temperature. PL was measured with an excitation wavelength of 371 nm. PLE was measured at emission wavelengths of 440 and 501 nm.\r\n10.1021/ic061555j,Ethylenediammonium oxalate lead iodide tetrahydrate,[(H2en)7(C2O4)2](Pb4I18)·4H2O,Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate,C18H78N14O12,\"Pb4I18, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, K2C2O4·H2O, ethylendiamine, HI, ethanol\",Yellow crystals,\"PbI2, K2C2O4·H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals formed.\",Thermogravimetric Analysis (TGA),TGA was performed on a Netzsch Sta449C thermoanalyzer in a nitrogen atmosphere over the range of 25-1000 degrees Celsius at a heating rate of 15 degrees per minute. This is dynamic thermogravimetry.\r\n10.1021/ic401215x,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,single crystal,,,,,,,,\"CH3NH3I [from synthesis], SnI2 [from synthesis], distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",Black MASnI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, elongated, rhombic dodecahedral (12 faces) crystals of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Formamidinium tin iodide,CH5N2SnI3,\"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",CH5N2,\"SnI3, Tin iodide\",Imidoformamidinium tin (II) iodide,3,single crystal,,,,,,,,\"HC(NH2)2I [from synthesis], SnI2 [from synthesis], distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",Black FASnI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black rhombic dodecahedral crystals (12 faces) of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"CH3NH3I [from syn], PbI2 [from syn], distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",Black MAPbI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, rhombic dodecahedral crystals (12 faces) of the title compound precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,single crystal,,,,,,,,\"HC(NH2)2I, PbI2, distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",Black FAPbI3 Crystals (α phase),\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Stop stirring and leave solution to evaporate at 100 °C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. After standing for 2-3 h at 100 °C, under a nitrogen atmosphere, set temperature to 80 °C for a further 2-3 h. Repeat the previous step for two more times to reach 60 °C and 40 °C at which point the solution was left to come to room temperature by powering off the hotplate. The crystals were collected by filtration and washed with anhydrous EtOH.\",Optical-diffuse reflectance,\"Optical diffuse-reflectance measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,powder,,,,,,,,\"CH3NH3I, SnI2\",Black MASnI3 Solid,\"Load equimolar amounts of SnI2 and MAI in a 9mm pyrex tube. Shake materials mechanically to ensure a homogenous mixture. Place tube on a sealing line evacuated to 10-4 mbar and flame sealed. Immerse tube on a sand bath standing at 200 °C, such that the mixture of solids was heated homogeneously. Maintain 4/5 of the tube outside the bath at room temperature. Leave solids in the bath for 2 h to form a homogeneous black solid. The Sn containing solids are air sensitive. No obvious color changes are observed.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,bulk polycrystalline,,,,,,,,\"CH3NH3I, PbI2\",Black MAPbI3 Solid,\"Load equimolar amounts of PbI2 and MAI in a 9mm pyrex tube. Shake materials mechanically to ensure a homogenous mixture. Place the tube on a sealing line evacuated to 10-4 mbar and flame sealed. Immerse tube on a sand bath standing at 200 °C, such that the mixture of solids was heated homogeneously. Maintain 4/5 of the tube outside the bath at room temperature. Leave solids in the bath for 2 h to form a homogeneous black solid.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,bulk polycrystalline,,,,,,,,\"CH3NH3I, SnI2\",Black MASnI3 Ingot,\"Load equimolar amounts of SnI2 and MAI in a 15mm pyrex test tube. Shake materials mechanically to ensure a homogenous mixture. Immerse in a sand bath standing at 350 °C under a gentle flow of nitrogen. The reaction proceeds within 0.5-1 min. The formation of a homogeneous black melt signals the end of the reaction. Upon melting the tube was removed from the bath and left to cool in air, usually producing a shiny black ingot.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,bulk polycrystalline,,,,,,,,\"CH3NH3I, PbI2\",Black MAPbI3 Ingot,\"Load equimolar amounts of PbI2 and MAI in a 15mm pyrex test tube. Shake materials mechanically to ensure a homogenous mixture. Immerse in a sand bath standing at 350 °C under a gentle flow of nitrogen. The reaction proceeds within 0.5-1 min. Pb-containing solids decompose on prolonged heating (> 3 min) or by raising the temperature above 400 °C, through evolution of I2 gas, crystallizing on the cooler walls of the tube.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,powder,,,,,,,,\"CH3NH3I, SnI2\",Black MASnI3 Powder,\"Place equimolar amounts of SnI2 and MAI in an agate mortar and ground carefully with a pestle until a visually homogeneous, black powder is obtained.\",Optical-diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CH3NH3I, PbI2\",Black MAPbI3 Powder,\"Place equimolar amounts of PbI2 and MAI in an agate mortar and ground carefully with a pestle until a visually homogeneous, black powder is obtained.\",Optical diffuse reflectance,\"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka−Munk equation: α/S =(1 − R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\"\r\n10.1021/ic401215x,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,single crystal,,,,,,,,\"CH3NH3I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",Black MASnI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, elongated, rhombic dodecahedral (12 faces) crystals of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 1.\"\r\n10.1021/ic401215x,Formamidinium tin iodide,CH5N2SnI3,\"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",CH5N2,\"SnI3, Tin iodide\",Imidoformamidinium tin (II) iodide,3,single crystal,,,,,,,,\"HC(NH2)2I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",Black FASnI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black rhombic dodecahedral crystals (12 faces) of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 1.\"\r\n10.1021/ic401215x,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"CH3NH3I [from syn], PbI2 [from syn], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",Black MAPbI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave solution to cool back to room temperature. Upon cooling, black, rhombic dodecahedral crystals (12 faces) of the title compound precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 1.\"\r\n10.1021/ic401215x,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,single crystal,,,,,,,,\"HC(NH2)2I, PbI2,distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",Black FAPbI3 Crystals (alpha phase),\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Stop stirring and leave the solution to evaporate at 100 °C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. After standing for 2-3 h at 100 °C, under a nitrogen atmosphere, set the temperature to 80 °C for a further 2-3 h. Repeat the previous step for two more times to reach 60 °C and 40 °C at which point the solution was left to come to room temperature by powering off the hotplate. The crystals were collected by filtration and washed with anhydrous EtOH.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to page 9025 Table 1.\"\r\n10.1021/ic401215x,Methylammonium tin iodide,CH3NH3SnI3,\"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",CH3NH3,\"SnI3, Tin iodide\",methanammonium tin(II) iodide,3,single crystal,,,,,,,,\"CH3NH3I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",Black MAPbI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate the solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, elongated, rhombic dodecahedral (12 faces) crystals of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\"\r\n10.1021/ic401215x,Formamidinium tin iodide,CH5N2SnI3,\"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",CH5N2,\"SnI3, Tin iodide\",Imidoformamidinium tin (II) iodide,3,single crystal,,,,,,,,\"HC(NH2)2I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",Black FASnI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate the solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black rhombic dodecahedral crystals (12 faces) of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\"\r\n10.1021/ic401215x,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"CH3NH3I [from syn], PbI2 [from syn], distilled HI 57% (99.95%), H3PO2 50%\",Black MAPbI3 crystals,\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Discontinue stirring and leave solution to cool back to room temperature. Upon cooling, black, rhombic dodecahedral crystals (12 faces) of the title compound precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\"\r\n10.1021/ic401215x,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,single crystal,,,,,,,,\"HC(NH2)2I, PbI2, distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",Black FAPbI3 Crystals (alpha phase),\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Stop stirring and leave solution to evaporate at 100 °C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. After standing for 2-3 h at 100 °C, under a nitrogen atmosphere, set temperature to 80 °C for a further 2-3 h. Repeat the previous step for two more times to reach 60 °C and 40 °C at which point the solution was left to come to room temperature by powering off the hotplate. The crystals were collected by filtration and washed with anhydrous EtOH.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\"\r\n10.1021/ic401215x,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,single crystal,,,,,,,,\"HC(NH2)2I, PbI2, distilled HI 57% (99.95%), H3PO2 50%\",Yellow FAPbI3 Crystals (delta phase),\"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 °C. Stop stirring and leave solution to evaporate at 100 °C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. Discontinue heating and cool the mixture to room temperature. After 4-5 h the black crystals fully convert to yellow ones of essentially the same shape. Collect yellow crystals by filtration and wash copiously with anhydrous EtOH. Yield 50-60%. The crystals are insensitive on exposure to the atmosphere but spontaneously hydrolyse to yellow PbI2 upon wetting in H2O.\",Single crystal X-ray diffraction,\"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 3.\"\r\n10.1021/ic500554z,Tetrakis(pentylammonium) cadmium chloride,C20H48N4Cd3Cl10,\"[C5H9NH3]4Cd3Cl10, tetrakis(pentane-1-aminium) decachloro tricadmate(II)\",C5H12N,\"Cd3Cl10, Cadmium chloride\",tetetrakis(pentane-1-aminium) cadmium chloride,2,single crystal,,,,,,,,\"Concentrated HCl, Cyclopentamine, Cadmium Chloride (CdCl2)\",Colorless block-shaped crystals,\"Cyclopentylamine (1.70 g, 0.02 mol) was taken in water (30 mL). Concentrated HCl (4.00 g, 0.04 mol) was added dropwise to it. The obtained solution mixture was added to an aqueous solution of CdCl2 (3.42 g, 0.015 mol). Slow evaporation of the solution at room temperature forms the crystals.\",Single crystal X-ray diffraction,Frames were collected on a Rigaku Saturn 924 diffractometer with Mo Kα radiation (λ = 0.71073 Å).\r\n10.1021/ic5025795,Bis(tropylium) tin iodide,C14H14SnI6,\"Bis(tropylium) hexaiodostannate(IV), (C7H7)2SnI6\",C7H7,\"SnI6, tin iodide\",bis(Tropylium) tin (IV) iodide,0,single crystal,,,,,,,,\"HI (57% aq., 1.5% H3PO2), tropylium tetrafluoroborate (99.99%, Sigma-Aldrich), tin metal shot (Sn, reagent grade, Alfa Aesar, iodine ( I2, 99.8%))\",Black (C7H7)2SnI6 powder,\"SnI4 was synthesized in an evacuated fused silica ampule (P < 10 mTorr) by reacting Sn (2.62 mmol) and I2 (5.26 mmol) in a furnace at 200 °C for 48 h.\r\nTropylium iodide was synthesized by reacting tropylium tetrafluoroborate (0.5177 g, 2.91 mmol) with HI.\r\nFor the preparation of (C7H7)2SnI6,  SnI4 (0.1834 g, 0.292 mmol) was dissolved in 7 mL HI in N2 atmosphere by heating at 100 °C and stirring. To it tropylium iodide (0.1279 g, 0.586 mmol) was added. The solution was stirred for an additional 15 min, at which time the heat was removed and the flask was allowed to air-cool while stirring gently. The solution and precipitate were washed with anhydrous ether and centrifuged three times. The black product was dried at 37 °C for 24 h.\",Powder X-ray diffraction + powder neutron diffraction,\"PXRD data were obtained from the diffractometer on beamline 11-BM-B at the Advanced Photon Source, Argonne National Laboratory. Neutron diffraction data were collected at the Spallation Neutron Source (SNS) at the Oak Ridge National Laboratory using the POWGEN diffractometer (BL-11A).\"\r\n10.1021/ic5025795,Tropylium Lead Iodide,C7H7PbI3,\"Tropylium triiodoplumbate(II), (C7H7)+PbI3\",C7H7,\"PbI3, Lead iodide\",tropylium lead (II) iodide,1,single crystal,,,,,,,,\"HI (57% aq., 1.5% H3PO2), tropylium tetrafluoroborate (99.99%, Sigma-Aldrich), lead iodide\r\n (PbI2), iodine ( I2, 99.8%))\",Red C7H7PbI3 powder,\"For the preparation of C7H7PbI3, PbI2 (0.6438 g, 1.395 mmol) was dissolved in 11 mL HI in N2 atmosphere by heating at 45 °C and stirring. The mixture was heated using an oil bath to 55 °C and tropylium tetrafluoroborate (0.2483 g, 1.396 mmol) was added. The heating was stopped and the solution was allowed to cool under gentle stirring to 40 °C. Then, the solution was taken out of N2 environment and was allowed to air cool in the oil bath. Once cool, the solution and red precipitate were washed with ethanol and centrifuged. The remaining product was then washed with anhydrous ether and centrifuged three times. The resulting bright red precipitate was dried at 37 °C for 24 h.\",Powder X-ray diffraction + powder neutron diffraction,\"PXRD data were obtained from the diffractometer on beamline 11-BM-B at the Advanced Photon Source, Argonne National Laboratory. Neutron diffraction data were collected at the Spallation Neutron Source (SNS) at the Oak Ridge National Laboratory using the POWGEN diffractometer (BL-11A).\"\r\n10.1021/ic700924j,\"N,N‘-dimethylethylenediammonium manganese formate\",C4H14N2Mn2C6H6O12,[CH3NH2(CH2)2NH2CH3][Mn2(HCOO)6],C4H14N2,\"[Mn2(HCOO)6]2-, Manganese formate\",\"bis(N,N'-dimethylethane-1,2-diaminium) manganese formate\",3,single crystal,,,,,,,,\"N,N′-dimethylethylenediamine (dmen), formic acid (HCOOH), methanol, Mn(ClO4)2‚6H2O\",Colorless needle-like crystals,0.35 g of dmen and 0.40 g of HCOOH were mixed in 10 mL of methanol. 2 mL of this solution was mixed with 2.0 mL of a 0.20 M methanol solution of Mn(ClO4)2‚6H2O.,Single crystal X-ray diffraction,Data were collected on a Nonius Kappa CCD diffractometer using graphite-monochromated Mo Kα (λ = 0.710 73 Å) radiation.\r\n10.1021/ic700924j,\"N,N‘-dimethylethylenediammonium copper formate\",C4H14N2Cu2C6H6O12,[CH3NH2(CH2)2NH2CH3][Cu2(HCOO)6],C4H14N2,\"[Co2(HCOO)6]2-, Copper formate\",\"bis(N,N'-dimethylethane-1,2-diaminium) copper formate\",3,single crystal,,,,,,,,\"N,N′-dimethylethylenediamine (dmen), formic acid (HCOOH), methanol, Co(ClO4)2‚6H2O\",Red block-like crystals,0.35 g of dmen and 0.40 g of HCOOH were mixed in 10 mL of methanol. 2 mL of this solution was mixed with 2.0 mL of a 0.20 M methanol solution of Co(ClO4)2‚6H2O.,Single crystal X-ray diffraction,Data were collected on a Nonius Kappa CCD diffractometer using graphite-monochromated Mo Kα (λ = 0.710 73 Å) radiation.\r\n10.1021/ja00006a076,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,,,,,\r\n10.1021/ja00124a012,Tris(iodoformamidinium) tin iodide,C3H12I3N6SnI5,\"tris(iododiaminomethanide) pentaiodostannate(II),[NH2C(I)==NH2]3Snl5\",CH4IN2,\"SnI5, Tin iodide\",tris(iododiaminomethanide) tin iodide,1,single crystal,,,,,,,,\"NH2CN, Snl2, aqueous HI (57 wt%)\",Column-like orange crystals,\"Dissolve 0.5 g of NH2CN (0.126 g, 3.0 mmol) and Snl2 (0.374 g, 1 mmol) in 10 mL of 57 wt % aqueous HI solution at 80 °C. Cool the solution from 80 to -10 °C at 2 °C/h. Filter the crystalline products under nitrogen from which, obtain column-like orange crystals. Dry the products in flowing argon at 80 °C for several hours and then remove to an argon-filled drybox with oxygen and water levels maintained below 1 ppm. Separate the orange crystals from the transparent iodoformamidinium iodide crystals.\",Single-crystal X-ray diffraction,Enraf-Nonius CAD4 diffractometer with graphite monochromatized Mo Ka radiation (λ = 0.7093 Å).\r\n10.1021/ja00124a012,Tris(iodoformamidinium) lead iodide,C3H12I3N6Pbl5,\"tris(iododiaminomethanide) pentaiodoplumbate(II), [NH2C(I)==NH2]3Pbl5\",CH4IN2,\"PbI5, Lead iodide\",tris(iododiaminomethanide) lead (II) iodide,1,single crystal,,,,,,,,\"CH3NH2•HI, NH2CN, Pbl2, aqueous HI (57 wt%)\",Yellow transparent crystals,\"Dissolve a 1:1:1 molar ratio of CH3NH2•HI (0.480 g, 3.02 mmol), NH2CN (0.127 g, 3.02 mmol), and Pbl2 (1.393 g, 3.02 mmol). Dissolve the reactants in 17 mL of 57 wt % aqueous hydriodic acid at 60°C. Soak the solution at 60°C for 24 h before cooling to -10°C at 2°C/h. Hold the crystals at -10°C for 10 h, filter the crystals and dry.\",Single-crystal X-ray diffraction,Enraf-Nonius CAD4 diffractometer with graphite monochromatized Mo Ka radiation (λ = 0.7093 Å).\r\n10.1021/ja206171,methylviologen BiI3Cl2,(MV)BiI3Cl2,Methylviologen dichloro triiodo bismuthate(III),C12H14N2,\"BiI3Cl2, Bismuth chloride iodide\",\"1,1′-Dimethyl-4,4′-bipyridinium bismuth triiodide dichloride\",1,single crystal,,,,,,,,\"BiCl3, 4,40-bipyridine, concentrated HCl and HI in methanol\",(MV)[BiI3Cl2] single crystal with face sizes up to 0.4 mm,\"Mix 0.4 mmol of BiCl3, 0.4 mmol of 4,40-bipyridine, 10 mL of MeOH, 1,7 mL of HCl (36%), and 0.1 mL of HI (57%) in a 25 mL Teflon bomb. Seal bomb in a Parr autoclave and heat in a programmable oven with the following parameters: heat from 25 to 150 °\u0001C over 2 h, hold at 150 \u0001°C for 13 h, and then cool to 25 °\u0001C over 10 h. A mixture of dark (MV)[BiI3Cl2] crystals and yellow (MV)4[Bi6Cl26] crystals in a ratio of ∼9:1 grew. Collect by filtration and wash with methanol.\",X-ray diffraction,Collected on a Bruker-Nonius Kappa-CDD diffractometer equipped with graphite monochromatized Mo Kα radiation (λ = 0.71073 Å).\r\n10.1021/ja301539s,Cesium tin iodide,CsSnI3,\"Cesium triiodostannate(II), CsSnI3\",None,\"SnI3, Tin iodide\",,3,single crystal,,,,,,,,\"CsI, SnI2\",black crystals,A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 ºC for 60 minutes. The mixture then cooled for 6 hours to room temperature.,single-crystal X-ray diffraction,\"Frames were collected using an STOE IPDS 2T diffractometer. Mo Kα radiation (50 kV, 40 mA, 34 cm diameter imaging plate) was used. Frames were collected with a 3 min exposure time and 1.0ω rotation. Absorption corrections, data extractions, and integrations were performed with X-AREA, X-RED, and X-SHAPE. Finally, the SHELXTL software package was used to refine/solve the structure.\"\r\n10.1021/ja301539s,Cesium tin iodide,CsSnI3,\"Cesium triiodostannate(II), CsSnI3\",None,\"SnI3, Tin iodide\",,3,single crystal,,,,,,,,\"CsI, SnI2\",black crystals,A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 ºC for 60 minutes. The mixture then cooled for 6 hours to room temperature.,UV-vis absorption (diffuse reflectance),The spectrum was recorded using a Shimadzu UV-3101 PC spectrometer. The reflectance data was converted to absorbance using the Kubelka-Munk equation.\r\n10.1021/ja301539s,Cesium tin iodide,CsSnI3,\"Cesium triiodostannate(II), CsSnI3\",None,\"SnI3, Tin iodide\",,3,powder,,,,,,,,\"CsI, SnI2\",black crystals (orthorhombic phase),A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 ºC for 60 minutes. The mixture then cooled for 6 hours to room temperature.,,\r\n10.1021/ja301539s,Cesium tin iodide,CsSnI3,\"Cesium triiodostannate(II), CsSnI3\",None,\"SnI3, Tin iodide\",,3,single crystal,,,,,,,,\"CsI, SnI2\",black crystals (orthorhombic phase),A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 ºC for 60 minutes. The mixture was then cooled for 6 hours to room temperature.,Electrical conductivity,Ingots were cut to the size of ~2mm x 3 mm x 8 mm in N2. These samples were then cut into rectangles. These samples were measured under He atmosphere in temperatures ranging from 300 K to 650 K. A ULVAC-RIKO ZEM-3 instrument system was used. Mechanical electrodes made of Rh-Pt and Pt made direct contact with ingot (no chemical paste).\r\n10.1021/ja301539s,Cesium tin iodide,CsSnI3,\"Cesium triiodostannate(II), CsSnI3\",None,\"SnI3, Tin iodide\",,1,single crystal,,,,,,,,\"CsI, SnI2\",yellow crystals,\"A stoichiometric mixture of CsI and SnI2 (total mass ~ 0.3 g) reacted in ethylenediamine (0.2 mL) in an evacuated Pyrex tube at 140 ºC for 3 days. Then, crack- and bubble-free ingots (~6 g) were prepared via the vertical Bridgeman technique; that is, pure CsSnI3 powder in an evacuated fused silica tube was passed down a single-zone Bridgeman furnace.\",UV-vis absorption (diffuse reflectance),\"The spectrum was recorded using a Shimadzu UV-3101 PC spectrometer. The reflectance data were converted to absorbance using the Kubelka-Munk equation:: α/S = (1-R)^{2}/(2R), where R = reflectance, α= absorption coefficient, S = scattering coefficient.\"\r\n10.1021/ja301539s,Cesium tin iodide,CsSnI3,\"Cesium triiodostannate(II), CsSnI3\",None,\"SnI3, Tin iodide\",,3,powder,,,,,,,,\"CsI, SnI2\",black crystals,A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 ºC for 60 minutes. The mixture then cooled for 6 hours to room temperature.,UV-vis absorption,\"Optical diffuse reflectance measurements were executed with a Shimadzu UV-3101 PC spectrometer (operating between 200 and 2500 nm). Reflectance was converted to absorption data with the Kubelka-Munk equation: α/S = (1-R)^{2}/(2R), where R = reflectance, α= absorption coefficient, S = scattering coefficient.\"\r\n10.1021/ja301539s,Cesium tin iodide,CsSnI3,\"Cesium triiodostannate(II), CsSnI3\",None,\"SnI3, Tin iodide\",,3,powder,,,,,,,,\"CsI, SnI2\",black crystals,A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 ºC for 60 minutes. The mixture then cooled for 6 hours to room temperature.,,\r\n10.1021/ja411045r,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,powder,,,,,,,,\"HBr, N1-methylethane-1,2-diamine, PbBr2\",Colorless plate-like crystals,\"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 ˚C. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",Photoluminescence,Emission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja411045r,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorbance,Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja411045r,\"N-methylpropane-1,3-diammonium lead bromide\",C4H14N2PbBr4,\"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N-methylpropane-1,3-diaminium lead(II) bromide\",2,powder,,,,,,,,\"HBr, N1-methylpropane-1,3-diamine, PbBr2\",Pale-yellow crystals,\"N1 -methylpropane-1,3-diammonium (N-MPDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylpropane-1,3-diamine (0.5 mL, 4.8 mmol) at 0 ˚C. The solvent was removed, and the resulting solid was washed with cold acetone. Finally, the solid was held under reduced pressure for 12 h to obtain (N-MPDA)Br2 as a colorless, crystalline solid. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MPDA)Br2 (0.067 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12 h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",Photoluminescence,Emission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja411045r,\"N-methylpropane-1,3-diammonium lead bromide\",C4H14N2PbBr4,\"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N-methylpropane-1,3-diaminium lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorbance,Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja411045r,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,single crystal,,,,,,,,\"HBr, N1-methylethane-1,2-diamine, PbBr2\",Colorless plate-like crystals,\"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 ˚C. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",Single crystal X-ray diffraction,Data were recorded in a Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and using monochromated Mo Kα (λ = 0.71073 Å) radiation.\r\n10.1021/ja411045r,\"N-methylpropane-1,3-diammonium lead bromide\",C4H14N2PbBr4,\"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N-methylpropane-1,3-diaminium lead(II) bromide\",2,single crystal,,,,,,,,\"HBr, N1-methylpropane-1,3-diamine, PbBr2\",Pale-yellow crystals,\"N1 -methylpropane-1,3-diammonium (N-MPDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylpropane-1,3-diamine (0.5 mL, 4.8 mmol) at 0 ˚C. The solvent was removed, and the resulting solid was washed with cold acetone. Finally, the solid was held under reduced pressure for 12 h to obtain (N-MPDA)Br2 as a colorless, crystalline solid. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MPDA)Br2 (0.067 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12 h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",Single crystal X-ray diffraction,Data were recorded in a Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and using monochromated Mo Kα (λ = 0.71073 Å) radiation.\r\n10.1021/ja411045r,\"N-methylpropane-1,3-diammonium lead bromide\",C4H14N2PbBr4,\"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N-methylpropane-1,3-diaminium lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorbance,Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja411045r,\"N-methylpropane-1,3-diammonium lead bromide\",C4H14N2PbBr4,\"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N-methylpropane-1,3-diaminium lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorbance,Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja411045r,\"N-methylpropane-1,3-diammonium lead bromide\",C4H14N2PbBr4,\"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N-methylpropane-1,3-diaminium lead(II) bromide\",2,powder,,,,,,,,\"HBr, N1-methylpropane-1,3-diamine, PbBr2\",Pale-yellow crystals,\"N1 -methylpropane-1,3-diammonium (N-MPDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylpropane-1,3-diamine (0.5 mL, 4.8 mmol) at 0 ˚C. The solvent was removed, and the resulting solid was washed with cold acetone. Finally, the solid was held under reduced pressure for 12 h to obtain (N-MPDA)Br2 as a colorless, crystalline solid. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MPDA)Br2 (0.067 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12 h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",Photoluminescence,Emission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja411045r,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorbance,Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja411045r,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorbance,Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja411045r,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,powder,,,,,,,,\"HBr, N1-methylethane-1,2-diamine, PbBr2\",Colorless plate-like crystals,\"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 ˚C. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",PLQE measurement using an integrating sphere,Princeton Instruments SpectraPro 500i spectrograph was used to collect the spectra. See supporting information page S3 for details.\r\n10.1021/ja411045r,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",2,powder,,,,,,,,\"HBr, N1-methylethane-1,2-diamine, PbBr2\",Colorless plate-like crystals,\"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 ˚C. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",UV-vis absorbance + Photoluminescence,\"Absorption was recorded in reflectance mode using a Shimadzu UV-2600 spectrometer equipped with an integrating sphere.\r\nEmission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\"\r\n10.1021/ja500618z,Guanidinium manganese formate,CH6N3MnC3HHO6,[C(NH2)3][Mn(HCOO)3],CH6N3,\"[Mn(HCOO)3]-, Manganese formate\",Guanidinium manganese formate,3,single crystal,,,,,,,,,,,Single crystal X-ray diffraction,\"Frames were collected using an Oxford Diffraction Gemini E Ultra diffractometer using Mo radiation ( λ=0.71073 Å, operating at 50 kV and 40 mA).\"\r\n10.1021/ja500618z,Azetidium manganese formate,C3H8NMnC3H3O6,[(CH2)3NH2][Mn(HCOO)3],C3H8N,\"[Mn(HCOO)3]-, Manganese formate\",azetidin-1-ium manganese formate,3,single crystal,,,,,,,,,,,Single crystal X-ray diffraction,\"Frames were collected using an Oxford Diffraction Gemini E Ultra diffractometer using Mo radiation ( λ=0.71073 Å, operating at 50 kV and 40 mA).\"\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead chloride\",C6H18N2O2PbCl4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",C6H18N2O2,\"PbCl4, Lead chloride\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",2,film,,,,,,,,,,,UV-vis absorption,\"Measured on spin-coated films using an Agilent Cary 6000i spectrometer\r\nin transmission mode.\"\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead chloride\",C6H18N2O2PbCl4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",C6H18N2O2,\"PbCl4, Lead chloride\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",2,powder,,,,,,,,\"PbCl2, HCl, 2,2’-(ethylenedioxy)bis(ethylamine)\",colorless solid,\"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (–70 ºC), stirred, 5.5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4].\",Photoluminescence,Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead chloride\",C6H18N2O2PbCl4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",C6H18N2O2,\"PbCl4, Lead chloride\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",2,film,,,,,,,,,,,UV-vis absorption,Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead chloride\",C6H18N2O2PbCl4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",C6H18N2O2,\"PbCl4, Lead chloride\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",2,powder,,,,,,,,\"PbCl2, HCl, 2,2’-(ethylenedioxy)bis(ethylamine)\",colorless solid,\"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (–70 ºC), stirred, 5.5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4].\",Photoluminescence,Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead chloride\",C6H18N2O2PbCl4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",C6H18N2O2,\"PbCl4, Lead chloride\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",2,powder,,,,,,,,\"PbCl2, HCl, 2,2’-(ethylenedioxy)bis(ethylamine)\",colorless solid,\"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (–70 ºC), stirred, 5.5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4].\",PLQE measurement using an integrating sphere,Absolute PLQE measurements were performed on powders on glass slides placed in an integrating sphere. Samples were excited using monochromatic light produced by a mercury-arc lamp and a monochromator fiber coupled to the sphere. The spectra of the emitted light and any unabsorbed excitation light were measured using a Princeton Instruments SpectraPro 500i spectrograph fiber-coupled to the sphere. See the supporting information for details.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead chloride\",C6H18N2O2PbCl4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",C6H18N2O2,\"PbCl4, Lead chloride\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",2,single crystal,,,,,,,,\"PbCl2, HCl, 2,2’-(ethylenedioxy)bis(ethylamine)\",Plate-like crystals,\"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (–70 ºC), stirred, 5.5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4]. Crystals suitable for x-ray structure determination were obtained through diffusion of diethyl ether into a 4-mL solution of the product (0.10 g, 0.20 mmol) in 12-M HCl.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and Mo Kα radiation (λ = 0.71073 Å).\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead bromide\",C6H18N2O2PbBr4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",C6H18N2O2,\"PbBr4, Lead bromide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorption,Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead bromide\",C6H18N2O2PbBr4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",C6H18N2O2,\"PbBr4, Lead bromide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",2,powder,,,,,,,,\"PbBr2, HBr, 2,2’-(ethylenedioxy)bis(ethylamine)\",colorless solid,\"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (–70 ºC), stirred, 5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4].\",Photoluminescence,Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead bromide\",C6H18N2O2PbBr4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",C6H18N2O2,\"PbBr4, Lead bromide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",2,film,,,,,,,,,,,UV-vis absorption,Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead bromide\",C6H18N2O2PbBr4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",C6H18N2O2,\"PbBr4, Lead bromide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",2,powder,,,,,,,,\"PbBr2, HBr, 2,2’-(ethylenedioxy)bis(ethylamine)\",colorless solid,\"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (–70 ºC), stirred, 5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4].\",Photoluminescence,Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead bromide\",C6H18N2O2PbBr4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",C6H18N2O2,\"PbBr4, Lead bromide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",2,powder,,,,,,,,\"PbBr2, HBr, 2,2’-(ethylenedioxy)bis(ethylamine)\",colorless solid,\"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (–70 ºC), stirred, 5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4].\",PLQE measurement using an integrating sphere,Absolute PLQE measurements were performed on powders on glass slides placed in an integrating sphere. Samples were excited using monochromatic light produced by a mercury-arc lamp and a monochromator fiber coupled to the sphere. The spectra of the emitted light and any unabsorbed excitation light were measured using a Princeton Instruments SpectraPro 500i spectrograph fiber-coupled to the sphere. See the supporting information for details.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead bromide\",C6H18N2O2PbBr4,\"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",C6H18N2O2,\"PbBr4, Lead bromide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",2,single crystal,,,,,,,,\"PbBr2, HBr, 2,2’-(ethylenedioxy)bis(ethylamine)\",Plate-like colorless crystals,\"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (–70 ºC), stirred, 5-mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4]. Crystals suitable for x-ray structure determination were obtained through diffusion of diethyl ether into a 2-mL solution of the product (0.20 g, 0.29 mmol) in 9-M HBr.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and Mo Kα radiation (λ = 0.71073 Å).\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead iodide\",C6H18N2O2PbI4,\"2,2′(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",C6H18N2O2,\"PbI4, Lead iodide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead iodide\",2,film,,,,,,,,,,,UV-vis absorption,Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead iodide\",C6H18N2O2PbI4,\"2,2′(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",C6H18N2O2,\"PbI4, Lead iodide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead iodide\",2,powder,,,,,,,,\"PbI2, HI, 2,2’-(ethylenedioxy)bis(ethylamine)\",yellow solid,\"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (–70 ºC), stirred, 5mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4].\",Photoluminescence,Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead iodide\",C6H18N2O2PbI4,\"2,2′(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",C6H18N2O2,\"PbI4, Lead iodide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead iodide\",2,film,,,,,,,,,,,UV-vis absorption,Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead iodide\",C6H18N2O2PbI4,\"2,2′(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",C6H18N2O2,\"PbI4, Lead iodide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead iodide\",2,powder,,,,,,,,\"PbI2, HI, 2,2’-(ethylenedioxy)bis(ethylamine)\",yellow solid,\"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (–70 ºC), stirred, 5mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4].\",Photoluminescence,Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead iodide\",C6H18N2O2PbI4,\"2,2′(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",C6H18N2O2,\"PbI4, Lead iodide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead iodide\",2,powder,,,,,,,,\"PbI2, HI, 2,2’-(ethylenedioxy)bis(ethylamine)\",yellow solid,\"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (–70 ºC), stirred, 5mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4].\",PLQE measurement using an integrating sphere,\"Absolute PLQE measurements were performed on powders on glass slides placed in an integrating sphere. Samples were excited using monochromatic light produced by a mercury-arc lamp and a monochromator fiber coupled to the sphere. The spectra of the emitted light and any unabsorbed excitation light were measured using a Princeton Instruments SpectraPro 500i spectrograph fiber-coupled to the sphere. \r\nSee the supporting information for details.\"\r\n10.1021/ja507086b,\"2,2′(ethylenedioxy)bis(ethylammonium) lead iodide\",C6H18N2O2PbI4,\"2,2′(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",C6H18N2O2,\"PbI4, Lead iodide\",\"2,2′(ethylenedioxy)bis(ethanaminium) lead iodide\",2,single crystal,,,,,,,,\"PbI2, HI, 2,2’-(ethylenedioxy)bis(ethylamine)\",yellow plate-like crystals,\"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (–70 ºC), stirred, 5mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 × 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4]. Crystals suitable for x-ray structure determination were obtained through diffusion of diethyl ether into a 3-mL solution of the product (0.20 g, 0.23 mmol) in 8-M HI.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and Mo Kα radiation (λ = 0.71073 Å).\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,single crystal,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\"thin, yellow-green plates\",\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",Single-crystal X-Ray diffraction,The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 Å (16 keV) radiation.\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,single crystal,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\"thin, yellow-green plates\",\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",Single-crystal X-Ray diffraction,The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 Å (16 keV) radiation.\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,single crystal,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\"thin, yellow-green plates\",\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",Single-crystal X-Ray diffraction,The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 Å (16 keV) radiation.\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,single crystal,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\"thin, yellow-green plates\",\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",Single-crystal X-Ray diffraction,The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 Å (16 keV) radiation.\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,powder,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",yellow-green powder,\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours.\",High-pressure optical absorption,The data were collected at the beamline U2A of the National Synchrotron Light Source (NSLS) at Brookhaven National Laboratory (BNL). Tauc plot with direct band gap assumption was used to obtain the band gap value.\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,pellet,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",yellow-green powder,\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at a reduced temperature for 12 hours.\",Cross-type DAC.,\"Solid sample was placed in insulating boron nitride gasket, which connected to 4 platinum leads. The leads lead into a sample cavity. Adjacent leads were coupled, the gasket was mounted into a cross-type DAC, and platinum leads were connected to external leads. The DAC was cooled to lower temperatures and raised to higher temperatures (between 274 and 310 K); each temperature was measured when the diamond was a consistent temperature. Current-voltage curves were generated from -40 to 40 mV at a scan rate of 1 mVs^{-1}, and conductivity was calculated by using slope of averaged curves, sample thickness, and distance between leads.\"\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,pellet,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",yellow-green powder,\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at a reduced temperature for 12 hours.\",resistivity measurements,Four platinum lead resistivity set-up was used in a diamond anvil cell (DAC).\r\n10.1021/ja512396m,\"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",C6H18O2N2CuCl4,\"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",C6H18O2N2,\"CuCl4, Copper chloride\",\"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",2,pellet,,,,,,,,\"2,2’-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",yellow-green powder,\"First, a 20mL solution of 2,2’-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at a reduced temperature for 12 hours.\",resistivity measurements,Four platinum lead resistivity set-up was used in a diamond anvil cell (DAC).\r\n10.1021/ja809598r,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"FTO (10 Ω/sq, Nippon Sheet Glass), TiCl4, HI, CH3NH2, PbI2\",\"MAPbI3 on TiO2-coated FTO, TiO2 film had a thickness of 8-12 μm. Powder is black.\",\"Soak FTO in a 40 mM TiCl4 aqueous solution at 70 °C for 30 min to form a thin TiO2 buffer layer. \r\n\r\nCoat FTO with a commercial nanocrystalline TiO2 paste (refer to SI for more information) using a screen printer and sintering at 480 °C for 1 h in air. \r\n\r\nSynthesize CH3NH3I by reacting HI with 40% methylamine in methanol solution followed by recrystallization.\r\n\r\nDrop the TiO2 film into an 8 wt % stoichiometric solution of CH3NH3I and PbI2 in γ-butyrolactone. Subsequent film formation was done by spin-coating.\",Powder X-ray diffraction,X-ray diffraction analysis (Rigaku RINT- 2500). Refer to Page 6050: Paragraph 2.\r\n10.1021/ja809598r,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,film,,,,,,,,\"FTO (10 Ω/sq, Nippon Sheet Glass), TiCl4, HBr, CH3NH2, PbBr2\",\"MAPbBr3 on TiO2-coated FTO, MAPbBr3 size 2-3mm. TiO2 film had a thickness of 8-12 μm. Powder is yellow\",\"Soak FTO in a 40 mM TiCl4 aqueous solution at 70 °C for 30 min to form a thin TiO2 buffer layer. \r\n\r\nCoat FTO with a commercial nanocrystalline TiO2 paste (refer to SI for more information) using a screen printer and sintering at 480 °C for 1 h in air.\r\n\r\nSynthesize CH3NH3Br by reacting HBr with 40% methylamine in methanol solution followed by recrystallization.\r\n\r\nDrop the TiO2 film into a 20 wt % stoichiometric solution of CH3NH3Br and PbBr2 in N,N-dimethylformamide. Subsequent film formation was done by spin-coating.\r\n\r\nThe liquid precursor film coated on the TiO2 gradually changed color simultaneously with drying, indicating the formation of CH3NH3PbBr3 in the solid state.\",Powder X-ray diffraction,X-ray diffraction analysis (Rigaku RINT- 2500). Refer to Page 6050: Paragraph 2.\r\n10.1021/jacs.0c00101,4-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",4-(methanaminium)pyridinium lead iodide,3,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",Orange plate-like crystals,\"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was being heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr..\",Single crystal X-ray diffraction (XRD),\"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ=0.71073 Å) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium 4-aminomethylpyridinium tin iodide,(3AMPY)0.5(4AMPY)0.5Sn2I6,*,C6H16N2,\"Sn2I6, Tin iodide\",piperidin-3-ylmethanaminium piperidin-4-ylmethanaminium tin iodide,3,single crystal,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (3AMPY, 99%), and 4-(aminomethyl)pyridine (4AMPY, 98%)\",dark red cube shaped crystals,\"SnCl2•2H2O (2 mmol, 451.3 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3AMPY and 4AMPY (0.5 mmol, 50.8 μL) were added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240º C and stirred for 5 minutes. Then, the temperature was lowered to 125 º C until red crystals formed.\",Single crystal X-ray diffraction (XRD),\"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ=0.71073 Å) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",3-(methanaminium)pyridinium lead iodide,3,powder,,,,,,,,\"PbO (99.9%), SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",red plate-like crystals,\"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240º C and stirred for 5 minutes. Then, the temperature was lowered to 125 º C until red crystals formed. After 1 hour, most crystals had formed, the product was obtained by suction filtration from hot solution, and finally fried for 30 more minutes.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using Tauc plot with indirect band gap approximation.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",3-(methanaminium)pyridinium lead iodide,3,unknown,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",red plate-like crystals,\"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240º C and stirred for 5 minutes. Then, the temperature was lowered to 125 º C until red crystals formed. After 1 hour, most crystals had formed, the product was obtained by suction filtration from hot solution, and finally fried for 30 more minutes.\",Raman spectroscopy,\"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",3-(methanaminium)pyridinium lead iodide,3,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",red plate-like crystals,\"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240º C and stirred for 5 minutes. Then, the temperature was lowered to 125 º C until red crystals formed. After 1 hour, most crystals had formed, the product was obtained by suction filtration from hot solution, and finally fried for 30 more minutes.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to obtain optical diffuse reflectance measurements. The reflectance v. wavelength data was converted to absorption v. wavelength using the Kubelka-Munk equation: α/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, α = absorption, and S = scattering coefficients.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",3-(methanaminium)pyridinium lead iodide,3,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O),  3-(aminomethyl)pyridine (98%)\",red plate-like crystals,\"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240º C and stirred for 5 minutes. Then, the temperature was lowered to 125 º C until red crystals formed.\",Single crystal X-ray diffraction,\"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ=0.71073 Å) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\"\r\n10.1021/jacs.0c00101,4-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",4-(methanaminium)pyridinium lead iodide,3,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",Orange plate-like crystals,\"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was heated and stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using Tauc plot with indirect band gap approximation.\"\r\n10.1021/jacs.0c00101,4-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",4-(methanaminium)pyridinium lead iodide,3,unknown,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",Orange plate-like crystals,\"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was heated and stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr.\",Raman spectroscopy,\"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters.\"\r\n10.1021/jacs.0c00101,4-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",4-(methanaminium)pyridinium lead iodide,3,powder,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",Orange plate-like crystals,\"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was heated and stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to obtain optical diffuse reflectance measurements. The reflectance v. wavelength data was converted to absorption v. wavelength using the Kubelka-Munk equation: α/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, α = absorption, and S = scattering coefficients.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium lead tin iodide,(3AMPY)(Pb1–xSnx)2I6 with x = 0.25,(3AMPY)(Sn/Pb)2I6,C6H16N2,Pb0.75Sn0.25,piperidin-3-ylmethanaminium lead (II) tin (II) iodide,3,single crystal,,,,,,,,\"PbO (99.9%), SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\"black, plated crystals\",\"SnCl2•2H2O (1.5 mmol) and 0.5 mmol PbO were dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated.\",Single crystal X-ray diffraction,\"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ=0.71073 Å) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium tin iodide,C6H10I6N2Sn2,\"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",3-(methanaminium)pyridinium tin iodide,3,single crystal,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\"black, plated crystals\",\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was being heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. Temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration and most product was formed within 1 hour.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using the Tauc plot with an indirect band gap approximation.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium tin iodide,C6H10I6N2Sn2,\"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",3-(methanaminium)pyridinium tin iodide,3,unknown,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\"black, plated crystals\",\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration.\",Raman spectroscopy,\"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium tin iodide,C6H10I6N2Sn2,\"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",3-(methanaminium)pyridinium tin iodide,3,powder,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\"black, plated crystals\",\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to obtain optical diffuse reflectance measurements. The reflectance v. wavelength data was converted to absorption v. wavelength using the Kubelka-Munk equation: α/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, α = absorption, and S = scattering coefficients.\"\r\n10.1021/jacs.0c00101,4-(aminomethyl)piperidinium tin iodide,C6H10I6N2Sn2,\"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",4-(methanaminium)piperidinium tin iodide,3,single crystal,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)-pyridine (98%)\",dark red plate-like crystals,\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",Single crystal X-ray diffraction,\"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ=0.71073 Å) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\"\r\n10.1021/jacs.0c00101,(3AMPY)0.5(4AMPY)0.5Sn2I6,C6H10I6N2Sn2,3-(methanaminium)pyridinium 4-(methanaminium)pyridinium hexaiodo distannate(II),C6H16N2,\"Sn2I6, Tin iodide\",3-(methanaminium)pyridinium 4-(methanaminium)pyridinium tin iodide,3,powder,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%), and 4-(aminomethyl)pyridine (98%)\",black plate-like crystals,\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.25 mmol, 50.8 μL) and 4AMPY (0.25 mmol) were added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using the Tauc plot with an indirect band gap approximation.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium tin iodide,C6H10I6N2Sn2,\"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",3-(methanaminium)pyridinium tin iodide,3,single crystal,,,,,,,,\"PbO (99.9%), SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%).\",black plate-like crystals,\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",Single crystal X-ray diffraction,\"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ=0.71073 Å) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\"\r\n10.1021/jacs.0c00101,4-(aminomethyl)piperidinium tin iodide,C6H10I6N2Sn2,\"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",4-(methanaminium)piperidinium tin iodide,3,single crystal,,,,,,,,\"PbO (99.9%), SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",dark red plate-like crystals,\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using the Tauc plot with an indirect band gap approximation.\"\r\n10.1021/jacs.0c00101,4-(aminomethyl)piperidinium tin iodide,C6H10I6N2Sn2,\"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",4-(methanaminium)piperidinium tin iodide,3,unknown,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",dark red plate-like crystals,\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",Raman spectroscopy,\"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters, and Raman scattering with frequencies as low as 10 cm^{-1} were obtained. Spectra ranged from -150 cm^{-1} to 200 cm^{-1}\"\r\n10.1021/jacs.0c00101,4-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",4-(methanaminium)pyridinium lead iodide,3,powder,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",dark red plate-like crystals,\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 μL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",UV-vis absorption,\"A Shimadzu UV-3600 UV-vis NIR spectrometer (used within the 200-2500 nm range at room temperature) was used to obtain optical diffuse reflectance measurements. BaSO4 was a reference. The reflectance v. wavelength data produced helped estimate bandgap of the material by converting reflectance to absorption using the Kubelka-Munk equation α/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, α = absorption, and S = scattering coefficients.\"\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",3-(methanaminium)pyridinium lead iodide,3,single crystal,SIESTA,DFT,GGA with revPBE,,Spin-orbit coupling,Core electrons: Troullier−Martins pseudopotentials; valence electrons are described by double-ζ polarized basis set with finite numerical pseudoatomic orbitals,Energy cutoff = 150 Ry,,,,,\r\n10.1021/jacs.0c00101,3-aminomethylpyridinium tin iodide,C6H10I6N2Sn2,\"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",3-(methanaminium)pyridinium tin iodide,3,single crystal,SIESTA,DFT,GGA with revPBE,,Spin-orbit coupling,Core electrons: Troullier−Martins pseudopotentials; valence electrons are described by double-ζ polarized basis set with finite numerical pseudoatomic orbitals,Energy cutoff = 150 Ry,,,,,\r\n10.1021/jacs.0c00101,4-aminomethylpyridinium lead iodide,C6H10I6N2Pb2,\"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",C6H16N2,\"Pb2I6, Lead iodide\",4-(methanaminium)pyridinium lead iodide,3,single crystal,SIESTA,DFT,GGA with revPBE,,Spin-orbit coupling,Core electrons: Troullier−Martins pseudopotentials; valence electrons are described by double-ζ polarized basis set with finite numerical pseudoatomic orbitals,Energy cutoff = 150 Ry,,,,,\r\n10.1021/jacs.0c00101,4-(aminomethyl)piperidinium tin iodide,C6H10I6N2Sn2,\"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",C6H16N2,\"Sn2I6, Tin iodide\",4-(methanaminium)piperidinium tin iodide,3,single crystal,SIESTA,DFT,GGA with revPBE,,Spin-orbit coupling,Core electrons: Troullier−Martins pseudopotentials; valence electrons are described by double-ζ polarized basis set with finite numerical pseudoatomic orbitals,Energy cutoff = 150 Ry,,,,,\r\n10.1021/jacs.0c00101,(3AMPY)0.5(4AMPY)0.5Sn2I6,C6H10I6N2Sn2,3-(methanaminium)pyridinium 4-(methanaminium)pyridinium hexaiodo distannate(II),C6H16N2,\"Sn2I6, Tin iodide\",3-(methanaminium)pyridinium 4-(methanaminium)pyridinium tin iodide,3,powder,,,,,,,,\"SnCl2•2H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%), and 4-(aminomethyl)pyridine (98%)\",black plate-like crystals,\"SnCl2•2H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.25 mmol, 50.8 μL) and 4AMPY (0.25 mmol) were added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240º C, and stirred for 5 minutes. The temperature was then lowered to 125º C until black crystals precipitated. Crystals were obtained via suction filtration.\",Single crystal X-ray diffraction (XRD),\"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ=0.71073 Å) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\"\r\n10.1021/jacs.0c01625,3-(aminomethyl)piperidinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",3-(aminomethyl)piperidinium diaminomethanide lead bromide,2,single crystal,,,,,,,,\"PbBr2 (98%), hydrobromic acid (HBr, 48%), formamidine acetate (99%), 3-(aminomethyl)piperidine\",yellow plate-like crystals,\"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, fomamidinium acetate (312 mg, 3 mmol) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg (0.5 mmol) of 3-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5- 10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",Single Crystal X-ray Diffraction,\"A STOE IPDS 2 or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\"\r\n10.1021/jacs.0c01625,3-(aminomethyl)piperidinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",3-(aminomethyl)piperidinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,,\r\n10.1021/jacs.0c01625,3-(aminomethyl)piperidinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",3-(aminomethyl)piperidinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,Photoluminescence microscopy,\"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\"\r\n10.1021/jacs.0c01625,3-(aminomethyl)piperidinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",3-(aminomethyl)piperidinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,,\r\n10.1021/jacs.0c01625,3-(aminomethyl)piperidinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",3-(aminomethyl)piperidinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,Photoluminescence microscopy,\"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\"\r\n10.1021/jacs.0c01625,3-(aminomethyl)piperindinium methylammonium lead bromide,(C6N2H16)(CH3NH3)Pb2Br7,\"(3AMP)(MA)Pb2Br7, 3-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\"C6N2H16, CH6N\",\"Pb2Br7, Lead bromide\",3-(methanaminium)piperindinium methanaminium lead bromide,2,single crystal,,,,,,,,\"PbBr2 (98%), hydrobromic acid (HBr, 48%), methylammonium chloride (≥98%), 3-(aminomethyl)piperidine\",yellow plate-like crystals,\"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, methylammonium chloride (202 mg) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg (0.5 mmol) of 3-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5- 10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",Single Crystal X-ray Diffraction,\"A STOE IPDS 2 or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\"\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium diaminomethanide lead bromide,2,single crystal,,,,,,,,\"PbBr2 (98%), hydrobromic acid (HBr, 48%), formamidine acetate (99%), 4-(aminomethyl)piperidine (96%)\",\"yellow, plate-like crystals\",\"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, fomamidinium acetate (312 mg, 3 mmol) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg of 4-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5-10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",Single Crystal X-ray Diffraction,\"A STOE IPDS 2 or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\"\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,,\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,Photoluminescence microscopy,\"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\"\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,,\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium formamidinium lead bromide,(C6N2H16)[HC(NH2)2]Pb2Br7,\"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\"C6N2H16, CH5N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,,,,Photoluminescence microscopy,\"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\"\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium methylammonium lead bromide,(C6N2H16)(CH3NH3)Pb2Br7,\"(4AMP)(MA)Pb2Br7, 4-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\"C6N2H16, CH6N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium methanaminium lead bromide,2,single crystal,,,,,,,,\"PbBr2 (98%), hydrobromic acid (HBr, 48%), methylammonium chloride (≥98%), 4-(aminomethyl)piperidine (96%)\",yellow plate-like crystals,\"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, methylammonium chloride (202 mg) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg of 4-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5- 10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",Single Crystal X-ray Diffraction,\"A STOE IPDS 2 or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\"\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium methylammonium lead bromide,(C6N2H16)(CH3NH3)Pb2Br7,\"(4AMP)(MA)Pb2Br7, 4-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\"C6N2H16, CH6N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium methanaminium lead bromide,2,bulk polycrystalline,,,,,,,,,,,,\r\n10.1021/jacs.0c01625,4-(aminomethyl)piperindinium methylammonium lead bromide,(C6N2H16)(CH3NH3)Pb2Br7,\"(4AMP)(MA)Pb2Br7, 4-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\"C6N2H16, CH6N\",\"Pb2Br7, Lead bromide\",4-(methanaminium)piperindinium methanaminium lead bromide,2,bulk polycrystalline,,,,,,,,,,,,\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic  acid (HI, 57  wt.  %  in  H2O, distilled, stabilized,   99.95%), hypophosphorous  acid  solution (H3PO2, 50  wt.  %  in  H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Single-crystal X-ray diffraction,\"A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ = 0.71073 Å) was used to perform the XRD. Data was collected, integrated, and corrected for absorption with the APEX3 software.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Single-crystal X-ray diffraction,\"A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ = 0.71073 Å) was used to perform the XRD. Data was collected, integrated, and corrected for absorption with the APEX3 software.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Single-crystal X-ray diffraction,\"A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ = 0.71073 Å) was used to perform the XRD. Data was collected, integrated, and corrected for absorption with the APEX3 software.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Photoluminescence,QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere. The PLQE was found by computing the ration of emitted photons to absorbed photons.\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,film,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",colorless 60 nm thick film,0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.,Photoluminescence,QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere. The PLQE was found by computing the ration of emitted photons to absorbed photons.\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",UV-vis absorption (diffused reflectance),\"A Shimadzu UV-3600 PC double-beam/double monochromator spectrophotometer was used to collect the data. The device was operated between 200 and 2500 nm. The non-absorbing reflectance reference was BaSO4. To find the estimated band gap of the material, the reflectance was converted to absorbance via the Kubelka-Munk equation.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,film,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",colorless 60 nm thick film,0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.,UV-vis absorption (diffused reflectance),\"A Shimadzu UV-3600 PC double-beam/double monochromator spectrophotometer was used to collect the data. The device was operated between 200 and 2500 nm. The non-absorbing reflectance reference was BaSO4. To find the estimated band gap of the material, the reflectance was converted to absorbance via the Kubelka-Munk equation.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",TGA measurement,A Netzsch Simultaneous Thermal Analysis (STA) system was used with around 15 mg of the sample. The sample was heated to 750ºC with a heating rate of 8ºC/min.\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",PL measurement,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,film,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",colorless 60 nm thick film,0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.,PL measurement,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Photoluminescence,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Photoluminescence,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Photoluminescence,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",Photoluminescence excitation,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,film,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",colorless 60 nm thick film,0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.,PL measurement,\"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\"\r\n10.1021/jacs.0c03004,\"1,8-octyldiammonium tin iodide\",(DAO)Sn2I6,\"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",C8N2H24,\"Sn2I6, Tin iodide\",\"1,8-octyldiaminium tin iodide\",1,single crystal,,,,,,,,\"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\"large, yellow, rectangular crystals\",\"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",UV-vis absorption (diffused reflectance),\"A Shimadzu UV-3600 PC double-beam/double monochromator spectrophotometer was used to collect the data. The device was operated between 200 and 2500 nm. The non-absorbing reflectance reference was BaSO4. To find the estimated band gap of the material, the reflectance was converted to absorbance via the Kubelka-Munk equation.\"\r\n10.1021/jacs.0c03860,Bis(butylammonium) methylammonium lead iodide,(BA)2(MA)Pb2I7,\"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\"C4NH12, CNH6\",\"Pb2I7, Lead iodide\",bis(butylaminium) methanaminium lead iodide,2,unknown,VASP,DFT,PBE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) methylammonium lead iodide,(BA)2(MA)Pb2I7,\"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\"C4NH12, CNH6\",\"Pb2I7, Lead iodide\",bis(butylaminium) methanaminium lead iodide,2,unknown,VASP,DFT,HSE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) methylammonium lead iodide,(BA)2(MA)Pb2I7,\"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\"C4NH12, CNH6\",\"Pb2I7, Lead iodide\",bis(butylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), methylammonium chloride, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",cherry red rectangular-shaped plates,\"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 μL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",UV-vis absorption,A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\r\n10.1021/jacs.0c03860,Bis(butylammonium) methylammonium lead iodide,(BA)2(MA)Pb2I7,\"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\"C4NH12, CNH6\",\"Pb2I7, Lead iodide\",bis(butylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), methylammonium chloride, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",cherry red rectangular-shaped plates,\"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 μL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",UV-vis absorption,A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\r\n10.1021/jacs.0c03860,Bis(butylammonium) methylammonium lead iodide,(BA)2(MA)Pb2I7,\"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\"C4NH12, CNH6\",\"Pb2I7, Lead iodide\",bis(butylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), methylammonium chloride, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",cherry red rectangular-shaped plates,\"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 μL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",Photoluminescence microscopy,A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\r\n10.1021/jacs.0c03860,Bis(butylammonium) methylammonium lead iodide,(BA)2(MA)Pb2I7,\"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\"C4NH12, CNH6\",\"Pb2I7, Lead iodide\",bis(butylaminium) methanaminium lead iodide,2,unknown,,,,,,,,\"PbO, HI, H3PO2, CH3NH3Cl, n-CH3(CH2)3NH2\",cherry red rectangular-shaped plates,\"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 μL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",,\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,powder,,,,,,,,\"PbO, FA acetate, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 μL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Powder X-ray diffraction,\"A Rigaku Miniflex600 powder X-ray diffractometer (Cu Kα graphite, λ = 1.5406 Å) was used. Operating settings included 40 kV/15 mA with Kβ foil filter.\"\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,powder,,,,,,,,\"PbO, FA acetate, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 μL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Powder X-ray diffraction,\"A Rigaku Miniflex600 powder X-ray diffractometer (Cu Kα graphite, λ = 1.5406 Å) was used. Operating settings included 40 kV/15 mA with Kβ foil filter.\"\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,unknown,VASP,DFT,PBE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,unknown,VASP,DFT,HSE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,unknown,VASP,DFT,PBE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,unknown,VASP,DFT,HSE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), FA acetate, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 μL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",UV-vis absorption,A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,unknown,,,,,,,,\"PbO, FA acetate, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 μL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Kubelka-Munk Equation,Reflectance vs. wavelength data was used with the Kubelka-Munk equation to estimate the band gap.\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), FA acetate, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 μL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Photoluminescence microscopy,A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\r\n10.1021/jacs.0c03860,Bis(butylammonium) formamidinium lead iodide,(C4H9NH3)2[CH(NH2)2PbI3]PbI4,\"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\"C4H12N, CH5N2\",Lead iodide,bis(butane-1-aminium) diaminomethanide lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), FA acetate, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 μL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Photoluminescence microscopy,A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,powder,,,,,,,,\"PbO, DMA chloride, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Powder X-ray diffraction,\"A Rigaku Miniflex600 powder X-ray diffractometer (Cu Kα graphite, λ = 1.5406 Å) was used. Operating settings included 40 kV/15 mA with Kβ foil filter.\"\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,powder,,,,,,,,\"PbO, DMA chloride, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Powder X-ray diffraction,\"A Rigaku Miniflex600 powder X-ray diffractometer (Cu Kα graphite, λ = 1.5406 Å) was used. Operating settings included 40 kV/15 mA with Kβ foil filter.\"\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,unknown,VASP,DFT,PBE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,unknown,VASP,DFT,HSE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,unknown,VASP,DFT,PBE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,unknown,VASP,DFT,HSE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",UV-vis absorption,A Shimadzu UV-3600 UV-vis NIR spectrometer (at 200-2500 nm region at 293 K) was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",UV-vis absorption,A Shimadzu UV-3600 UV-vis NIR spectrometer (at 200-2500 nm region at 293 K) was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Photoluminescence,A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\r\n10.1021/jacs.0c03860,Bis(butylammonium) dimethylammonium lead iodide,(BA)2(DMA)Pb2I7,\"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\"C4NH12, C2H8N\",\"Pb2I7, Lead iodide\",bis(butylaminium) dimethanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Photoluminescence,A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,powder,,,,,,,,\"PbO (99.9%), guanidinium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Powder X-ray diffraction,\"A Rigaku Miniflex600 powder X-ray diffractometer (Cu Kα graphite, λ = 1.5406 Å) was used. Operating settings included 40 kV/15 mA with Kβ foil filter.\"\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,powder,,,,,,,,\"PbO, GA chloride, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Powder X-ray diffraction,\"A Rigaku Miniflex600 powder X-ray diffractometer (Cu Kα graphite, λ = 1.5406 Å) was used. Operating settings included 40 kV/15 mA with Kβ foil filter.\"\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,unknown,VASP,DFT,PBE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,unknown,VASP,DFT,HSE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,unknown,VASP,DFT,PBE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,unknown,VASP,DFT,HSE+SOC,4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds,,PAW,,,,,,\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), guanidinium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",UV-vis absorption,A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,unknown,,,,,,,,\"PbO, GA chloride, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Kubelka-Munk Equation,Reflectance vs. wavelength data was used with the Kubelka-Munk equation to estimate the band gap.\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"PbO (99.9%), guanidinium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",Photoluminescence microscopy,A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\r\n10.1021/jacs.0c03860,Bis(butylammonium) guanidinium lead iodide,(BA)2(GA)Pb2I7,\"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\"C4NH12, CN3H8\",\"Pb2I7, Lead iodide\",bis(butylaminium) diaminomethanaminium lead iodide,2,unknown,,,,,,,,\"PbO, GA chloride, HI, BA, H3PO2\",red plate-shaped crystals,\"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 μL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125º C until crystals began to form. The temperature was lowered again to 80ºC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",,\r\n10.1021/jacs.0c03899,(R/S-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH3)2SnI4,\"(MBA)2SnI4, Œ±-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",(R/S-)methylbenzylaminium tin iodide,2,single crystal,,,,,,,,\"(R)-(+)-α-Methylbenzylamine (R-MBA, 98%, ee 96%), (S)-(−)-α-methylbenzylamine, (S-MBA, 98%, ee 98%), (±)-α-methylbenzylamine (rac-MBA, 99%), tTin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",Orange crystals,\"SnO2 (0.896 mmol), MBA (R-, S-, or rac-; 1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",Single-crystal X-ray diffraction,A Rigaku XtaLAB Synergy-S instrument using Mo Kalpha radiation was used for SCXRD at 250 K. The SHELXS program was used to directly solve the structure and the SHELXL program from the Olex2 package was used for refinement.\r\n10.1021/jacs.0c03899,(R/S-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH3)2SnI4,\"(MBA)2SnI4, Œ±-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",(R/S-)methylbenzylaminium tin iodide,2,film,,,,,,,,\"(±)-α-methylbenzylamine (rac-MBA, 99%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N,N-anhydrous DMF\",Thin film on quartz substrate,\"SnO2 (0.896 mmol), rac-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes.\",UV-vis absorption,A Cary 5000 UV-vis-NIR spectrometer operated in the 200-800 nm wavelength range was used to collect the absorption spectra. A blank quartz substrate was the 100% transmittance reference.\r\n10.1021/jacs.0c03899,(R/S-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH3)2SnI4,\"(MBA)2SnI4, Œ±-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",(R/S-)methylbenzylaminium tin iodide,2,film,,,,,,,,\"(R)-(+)-α-Methylbenzylamine (R-MBA, 98%, ee 96%), (S)-(−)-α-methylbenzylamine, (S-MBA, 98%, ee 98%), (±)-α-methylbenzylamine (rac-MBA, 99%), tTin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N,N-anhydrous DMF\",Thin film on quartz substrate,\"SnO2 (0.896 mmol), MBA (R-, S-, or rac-; 1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes. Linear optical and CD measurements were made on the quartz films, and mCP-AFM measurements were made on the FTO films.\",Circular Dichroism (CD) Spectroscopy,A Jasco J-715 spectropolarimeter was used for the CD measurements. 3-5 scans of the spectra were taken and averaged. A wavelength range of 200-600 nm was used with 0.2 nm resolution.\r\n10.1021/jacs.0c03899,(R/S-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH3)2SnI4,\"(MBA)2SnI4, Œ±-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",(R/S-)methylbenzylaminium tin iodide,2,film,,,,,,,,\"(R)-(+)-α-Methylbenzylamine (R-MBA, 98%, ee 96%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N, N-anhydrous DMF\",Thin-film on FTO substrate,\"SnO2 (0.896 mmol), R-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes.\",Magnetic conductive-probe atomic force microscopy,\"The mCP-AFM measurements were made using a Bruker Icon AFM system enclosed within an Argon glovebox. The specific tip used was the “Bruker MESP-V2”, and contact mode was selected. The Co-Cr coated tips were premagnetized through exposure to a strong permanent magnet for about an hour, scanning immediately afterwards. The magnetization of the tip causes the spin-degeneracy of the carriers in the tip to be lifted, causing mostly one spin-state to be injected into the sample. While scanning, the tip was grounded, and a bias was applied to the sample in the range of -1.2 to 1.2 V. A scan rate of 0.3 Hz was used. Over 100 I-V curves were generated and averaged at different locations on the sample for the three different magnetizations (north, south, none).\"\r\n10.1021/jacs.0c03899,(R/S-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH3)2SnI4,\"(MBA)2SnI4, Œ±-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",(R/S-)methylbenzylaminium tin iodide,2,film,,,,,,,,\"(S)-(−)-α-methylbenzylamine, (S-MBA, 98%, ee 98%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N, N-anhydrous DMF\",Thin film on FTO substrate,\"SnO2 (0.896 mmol), S-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes.\",Magnetic conductive-probe atomic force microscopy,\"The mCP-AFM measurements were made using a Bruker Icon AFM system enclosed within an Argon glovebox. The specific tip used was the “Bruker MESP-V2”, and contact mode was selected. The Co-Cr coated tips were premagnetized through exposure to a strong permanent magnet for about an hour, scanning immediately afterwards. The magnetization of the tip causes the spin-degeneracy of the carriers in the tip to be lifted, causing mostly one spin-state to be injected into the sample. While scanning, the tip was grounded, and a bias was applied to the sample in the range of -1.2 to 1.2 V. A scan rate of 0.3 Hz was used. Over 100 I-V curves were generated and averaged at different locations on the sample for the three different magnetizations (north, south, none).\"\r\n10.1021/jacs.0c03899,Bis(S-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH2)2SnI4,\"(S-MBA)2SnI4, bis(S-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",bis(S-)methylbenzylaminium tin iodide,2,single crystal,,,,,,,,\"(S)-(−)-α-methylbenzylamine, (S-MBA, 98%, ee 98%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",\"Orange, rod-like crystals\",\"SnO2 (0.896 mmol), S-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",single-crystal X-ray diffraction,\"A Rigaku XtaLAB Synergy-S instrument using Mo Kα radiation (λ = 0.71073 Å) is utilized to collect a full sphere of diffraction data at 250K and multiscan empirical absorption correction was applied. Within the Olex2 software, using direct methods of the SHELXS program to solve the crystal structure, then utilizing the least-squares method of the SHELXL58 program to refine it.\"\r\n10.1021/jacs.0c03899,Bis(R-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH2)2SnI4,\"(R-MBA)2SnI4, bis(R-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",bis(R-)methylbenzylaminium tin iodide,2,single crystal,,,,,,,,\"(R)-(+)-α-Methylbenzylamine (R-MBA, 98%, ee 96%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",\"Orange, rod-like crystals\",\"SnO2 (0.896 mmol), R-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",single-crystal X-ray diffraction,\"A Rigaku XtaLAB Synergy-S instrument using Mo Kα radiation (λ = 0.71073 Å) is utilized to collect a full sphere of diffraction data at 250K and multiscan empirical absorption correction was applied. Within the Olex2 software, using direct methods of the SHELXS program to solve the crystal structure, then utilizing the least-squares method of the SHELXL58 program to refine it.\"\r\n10.1021/jacs.0c03899,Bis(rac-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH2)2SnI4,\"(rac-MBA)2SnI4, bis(rac-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",bis(rac-)methylbenzylaminium tin iodide,2,single crystal,,,,,,,,\"(±)-α-methylbenzylamine (rac-MBA, 99%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",\"Orange, rod-like crystals\",\"SnO2 (0.896 mmol), rac-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",single-crystal X-ray diffraction,\"A Rigaku XtaLAB Synergy-S instrument using Mo Kα radiation (λ = 0.71073 Å) is utilized to collect a full sphere of diffraction data at 250K and multiscan empirical absorption correction was applied. Within the Olex2 software, using direct methods of the SHELXS program to solve the crystal structure, then utilizing the least-squares method of the SHELXL58 program to refine it.\"\r\n10.1021/jacs.0c03899,Bis(S-)methylbenzylammonium tin iodide,(C6H5CH(CH3)NH2)2SnI4,\"(S-MBA)2SnI4, bis(S-)methylbenzylaminium tetraiodostannate(II)\",C8H12N,\"SnI4, Tin iodide\",bis(S-)methylbenzylaminium tin iodide,2,single crystal,,,,,,,,,,,,\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb2I7,C19H31I7N3Pb2I7,Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb2I7, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",red crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",Single-crystal X-ray diffraction,Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ = 0.71073 Å) was used. Data were collected and corrected for absorption effects with APEX3 software.\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb2I7,C19H31I7N3Pb2I7,Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb2I7, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",red crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",,Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used.\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb2I7,C19H31I7N3Pb2I7,Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb2I7, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",red crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",UV-vis absorption (diffused reflectance),\"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference.\"\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb2I7,C19H31I7N3Pb2I7,Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb2I7, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",red crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",,\"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference. Wavelength used was λ = 0.71073 Å.\"\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb3I10,C20H40I10N4Pb3I10,Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb3I10, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",dark brown crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",single crystal X-ray diffraction,Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ = 0.71073 Å) was used. Data were collected and corrected for absorption effects with APEX3 software.\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb3I10,C20H40I10N4Pb3I10,Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb3I10, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",dark brown crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",,Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used.\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb3I10,C20H40I10N4Pb3I10,Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb3I10, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",dark brown crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",UV-vis absorption (diffused reflectance),\"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference.\"\r\n10.1021/jacs.0c09647,(PPA)2(MA0.5FA0.5)Pb3I10,C20H40I10N4Pb3I10,Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II),\"C9H12N, CNH6, CH5N2\",\"Pb3I10, Lead iodide\",,2,single crystal,,,,,,,,\"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium – I)\",dark brown crystals,\"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",,\"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference. Wavelength of λ = 0.71073 Å was used.\"\r\n10.1021/jacs.2c12034,N-methyl 3-iodopropylammonium lead iodide,C8N2H22PbI6,(MIPA)2PbI4,C4H11NI,PbI4,bis(3-iodo-N-methylpropan-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"Lead oxide (Sigma Aldrich, PbO, 99.9%), hydroiodic acid (Sigma Aldrich, HI, 57% w/w in water), hypophosphorous acid (Avra chemicals, H3PO2, 50% w/w in water), 3-methylamino 1-propanol (Sigma Aldrich, HO-(CH2)3-N(CH3)H, 96%)\",Orange plate-like crystals,\"2.5 mmol of PbO was dissolved in a mixture of 20 mL HI and 3 mL H3PO2 in a glass beaker at room temperature using sonication for 10 minutes in an ultrasonic bath sonicator. To this, 5 mmol of OH-(CH2)3- NH(CH3) (for MIPA) was added dropwise. The mixture was heated and stirred at 110 oC for 30 minutes using an oil bath placed on a heater and magnetic stirrer. After 30 minutes, the heating and stirring were stopped, and the clear yellow solution was allowed to cool undisturbed to room temperature. After 24 hours, the precipitated crystals were collected using suction filtration, washed with diethyl ether, and dried in the air.\",Single-crystal X-ray diffraction,\"Data were collected in a Bruker Apex Duo diffractometer using Mo Kα radiation (λ = 0.71 Å). The integrations of the collected data and numerical absorption corrections were done using APEX3 software. The structures were solved by the direct method using SHELXS and refined by full-matrix least-squares on F2 using the SHELXL, as implemented in Olex2.\"\r\n10.1021/jacs.2c12034,N-methyl 3-iodopropylammonium lead iodide,C8N2H22PbI6,(MIPA)2PbI4,C4H11NI,PbI4,bis(3-iodo-N-methylpropan-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"Lead oxide (Sigma Aldrich, PbO, 99.9%), hydroiodic acid (Sigma Aldrich, HI, 57% w/w in water), hypophosphorous acid (Avra chemicals, H3PO2, 50% w/w in water), 3-methylamino 1-propanol (Sigma Aldrich, HO-(CH2)3-N(CH3)H, 96%)\",Orange plate-like crystals,\"2.5 mmol of PbO was dissolved in a mixture of 20 mL HI and 3 mL H3PO2 in a glass beaker at room temperature using sonication for 10 minutes in an ultrasonic bath sonicator. To this, 5 mmol of OH-(CH2)3- NH(CH3) (for MIPA) was added dropwise. The mixture was heated and stirred at 110 oC for 30 minutes using an oil bath placed on a heater and magnetic stirrer. After 30 minutes, the heating and stirring were stopped, and the clear yellow solution was allowed to cool undisturbed to room temperature. After 24 hours, the precipitated crystals were collected using suction filtration, washed with diethyl ether, and dried in the air.\",Diffuse reflectance,The spectrum was recorded using a Shimadzu UV3600 plus UV−vis−NIR spectrophotometer with BaSO4 powder as a reference of 100% reflectance. The reflectance signal is converted to absorbance using the Kubelka−Munk function.\r\n10.1021/jacs.5b13294,Cesium silver bismuth bromide,Cs2AgBiBr6,Dicesium tribromoargentate(I) tribromobismuthate(III),None,AgBiBr6,,3,single crystal,,,,,,,,\"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",red-orange crystals,\"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110º C for 2 hours, and cooled to room temperature by controlling the cooling rate to 2ºC/hr or 1ºC/hr. The obtained crystals were filtered on a glass frit and dried under low pressure overnight.\",X-ray diffraction,\"A crystal was coated in Paratone-N oil, placed on a Kapton loop, and transferred to a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector. Data was collected using ωv and ψ scans with 18-keV synchrotron radiation (λ = 0.68880 Å)\"\r\n10.1021/jacs.5b13294,Cesium silver bismuth bromide,Cs2AgBiBr6,Dicesium tribromoargentate(I) tribromobismuthate(III),None,AgBiBr6,,3,powder,,,,,,,,\"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",orange powder,\"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterwards, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110º C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",Estimation through Tauc plot.,Cary 6000i UV-Vis spectrometer equipped with an integrating sphere was used in absorbance mode to collect absorption data. The powder was pressed and mounted on a quartz slide such that incident light was normal to the surface.\r\n10.1021/jacs.5b13294,Cesium silver bismuth bromide,Cs2AgBiBr6,Dicesium tribromoargentate(I) tribromobismuthate(III),None,AgBiBr6,,3,powder,,,,,,,,\"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",orange powder,\"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110º C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",UV-vis absorption,Cary 6000i UV-Vis spectrometer equipped with an integrating sphere was used in absorbance mode to collect absorption data. The powder was pressed and mounted on a quartz slide such that incident light was normal to the surface.\r\n10.1021/jacs.5b13294,Cesium silver bismuth bromide,Cs2AgBiBr6,Dicesium tribromoargentate(I) tribromobismuthate(III),None,AgBiBr6,,3,powder,,,,,,,,\"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",orange powder,\"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110º C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",Photoluminescence,Room-temperature steady-state emission spectra were collected on powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\r\n10.1021/jacs.5b13294,Cesium silver bismuth bromide,Cs2AgBiBr6,Dicesium tribromoargentate(I) tribromobismuthate(III),None,AgBiBr6,,3,powder,,,,,,,,\"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",orange powder,\"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110º C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",Photoluminescence,Low-temperature photoluminescence was measured using a spectrograph (Acton Research SpectraPro 500i) equipped with a silicon CCD array detector (Hamamatsu). Samples were cooled to liquid helium temperatures using a Janus ST-500 cold-finger cryostat.\r\n10.1021/jacs.6b03207,Cesium tin iodide,Cs2SnI6,Dicesium hexastannate(II),None,SnI6,,3,powder,,,,,,,,\"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), SnI4\",Black crystals,\"In a beaker, slowly add ∼0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve SnI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the SnI4 precursors gently to T ≈ 60 °C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the SnI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 °C for 24 h.\",Powder neutron diffraction,\"POWGEN diffractometer at the Spallation Neutron Source, Oak Ridge National Laboratory; Rietveld analysis\"\r\n10.1021/jacs.6b03207,Cesium tellurium iodide,Cs2TeI6,\"Dicesium hexatellurate(II), Cs2TeI6\",None,TeI6,,3,powder,,,,,,,,\"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), TeI4\",Black crystals,\"In a beaker, slowly add ∼0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve TeI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the TeI4 precursors gently to T ≈ 60 °C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the TeI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 °C for 24 h.\",Powder neutron diffraction,\"POWGEN diffractometer at the Spallation Neutron Source, Oak Ridge National Laboratory; Rietveld analysis\"\r\n10.1021/jacs.6b03207,Cesium tin iodide,Cs2SnI6,Dicesium hexastannate(II),None,SnI6,,3,powder,,,,,,,,\"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), SnI4\",Black crystals,\"In a beaker, slowly add ∼0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve SnI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the SnI4 precursors gently to T ≈ 60 °C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the SnI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 °C for 24 h.\",Powder X-ray diffraction,\"Data were collected at the 11-BM-B beamline at the Advanced Photon Source, Argonne National Laboratory.\"\r\n10.1021/jacs.6b03207,Cesium tellurium iodide,Cs2TeI6,\"Dicesium hexatellurate(II), Cs2TeI6\",None,TeI6,,3,powder,,,,,,,,\"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), TeI4\",Black crystals,\"In a beaker, slowly add ∼0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve TeI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the TeI4 precursors gently to T ≈ 60 °C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the TeI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 °C for 24 h.\",Powder X-ray diffraction,\"Data were collected at the 11-BM-B beamline at the Advanced Photon Source, Argonne National Laboratory.\"\r\n10.1021/jacs.7b01312,2-dimethylamino-1-ethylamine lead bromide,C4H14N2PbBr4,\"N,N,N-dimethylethanaminium tetrabromoplumbate(II), (DMEN)PbBr4,2-(dimethylamino)ethylamine, ((CH3)2NH(CH2)2NH3)PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N,N,N-dimethylethanaminium lead (II) bromide\",2,single crystal,,,,,,,,\"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 2-(dimethylamino)ethylamine\",colorless rhombic shaped crystals,\"0.669g PbO powder was added into 6.0 ml HBr and 1.0 mL of H3PO2 under stirring while heating at 150 °C until PbO was dissolved. 0.264g 2-(dimethylamino)ethylamine was added to the above solution under heating and stirring.\r\nAfter cooling and leaving the solution for 10-14 days, α-(DMEN)PbBr4 crystals were obtained.\",Single Crystal X-ray Diffraction,\"Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo Kα (λ = 0.71073 Å) radiation.\r\nIntegration and correction of the data were done by STOE X-AREA programs. Crystal structures were resolved by using OLEX2 program package by full-matrix least-squares on F^2.\"\r\n10.1021/jacs.7b01312,2-dimethylamino-1-ethylamine lead bromide,C4H14N2PbBr4,\"N,N,N-dimethylethanaminium tetrabromoplumbate(II), (DMEN)PbBr4,2-(dimethylamino)ethylamine, ((CH3)2NH(CH2)2NH3)PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N,N,N-dimethylethanaminium lead (II) bromide\",2,single crystal,,,,,,,,\"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 2-(dimethylamino)ethylamine\",pale yellow platelike crystals,0.669g PbO powder was added into 6.0 ml HBr and 1.0 mL of H3PO2 under stirring while heating at 150 °C until PbO was dissolved. 0.264g 2-(dimethylamino)ethylamine was added to the above solution under heating and stirring. The β-(DMEN)PbBr4 crystals were obtained during slow cooling.,Single Crystal X-ray Diffraction,Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo Kα (λ = 0.71073 Å) radiation. Integration and correction of the data is done by STOE X-AREA programs. Crystal structures is resolved by using OLEX2 program package by full-matrix least-squares on F^2.\r\n10.1021/jacs.7b01312,3-(dimethylamino)-1-propylamine lead bromide,C5H16N2PbBr4,\"3-(N,N-dimethanaminium)-propane-1-aminium tetrabromoplumbate(II), (DMAPA)PbBr4, [(CH3)2NH(CH2)3NH3]PbBr4\",C5H16N2,\"PbBr4, Lead bromide\",\"3-(N,N-dimethanaminium)-propane-1-aminium lead (II) bromide\",2,single crystal,,,,,,,,\"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 3-(dimethylamino)-1-propylamine\",pale yellow platelike crystal,\"0.892 g PbO powder was added to a mixture of 6.0 mL HBr and 1.0 mL H3PO2 under heating at 150°C and stirring for about 10 mins until all PbO dissolved. Separately, 1.0 mL HBr was added to 0.408 g 3-(dimethylamino)-1-propylamine.\r\nThe solutions were mixed at 150°C. During slow cooling, pale yellow platelike (DMAPA)PbBr4 crystals were formed.\",Single Crystal X-ray Diffraction,Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo Kα (λ = 0.71073 Å) radiation. Integration and correction of the data were done by STOE X-AREA programs. Crystal structures were resolved by using OLEX2 program package by full-matrix least-squares on F^2.\r\n10.1021/jacs.7b01312,4-dimethylaminobutylamine lead bromide,C6H18N2PbBr4,\"3-(N,N-dimethanaminium)-butane-1-aminium tetrabromoplumbate(II), (DMABA)PbBr4, [(CH3)2NH(CH2)4NH3]PbBr4\",C6H18N2,\"PbBr4, Lead bromide\",\"3-(N,N-dimethanaminium)-butane-1-aminium lead (II) bromide\",2,single crystal,,,,,,,,\"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 4-dimethylaminobutylaminee\",pale yellow platelike crystal,\"0.892 g PbO powder was added to a mixture of 6.0 mL HBr and 1.0 mL H3PO2 under heating at 150°C and stirring for about 10 mins until all PbO dissolved. Separately, 1.0 mL HBr was added to 0.500 g (4.3 mmol) of 4-dimethylaminobutylamine. The solutions were mixed at 150°C. During slow cooling, pale yellow platelike (DMABA)PbBr4 crystals were formed.\",Single Crystal X-ray Diffraction,Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo Kα (λ = 0.71073 Å) radiation. Integration and correction of the data were done by STOE X-AREA programs. Crystal structures were resolved by using OLEX2 program package by full-matrix least-squares on F^2.\r\n10.1021/jacs.7b01629,Bis(methylammonium) thallium bismuth bromide,C2H12N2BiBr6Tl,\"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",CH6N,\"TlBiBr6, Bismuth bromide thallium\",bis(methanaminium) bismuth thallium bromide,3,single crystal,,,,,,,,\"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide ((MA)Br)\",red octahedral single crystals,\"TlBr was prepared in lab by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. This resulted in clear, colorless solutions. Next, the (TBA)Br solution was added to the Tl(PF6) solution dropwise and under constant stirring. TlBr resulted as a yellow, solid precipitate and was filtered, washed with MeCN, and added to 1 mL of concentrated HBr, which contained BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The solution was sonicated for 5 minutes, resulting in an orange-red solid that transformed into a deep red. After one hour, the solid was isolated via filtration, residual solvent was removed, and 298 mg of solid yielded. The crystals sat, undisturbed, for 1 week at room temperature.\",Single crystal X-ray diffraction,\"Crystals were coated with Paratone-N oil, placed on a Kapton loop, and moved to a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector. Frames were collected with Mo-kα radiation. Frames were corrected for Lorentz and polarization effects using SAINT 8.27b and absorption effects using SADABS V2012. Structure was solved by direct methods and via SHELXL-2013 software.\"\r\n10.1021/jacs.7b01629,Bis(methylammonium) thallium bismuth bromide,C2H12N2BiBr6Tl,\"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",CH6N,\"TlBiBr6, Bismuth bromide thallium\",bis(methanaminium) bismuth thallium bromide,3,unknown,,,,,,,,,,,,\r\n10.1021/jacs.7b01629,Bis(methylammonium) thallium bismuth bromide,C2H12N2BiBr6Tl,\"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",CH6N,\"TlBiBr6, Bismuth bromide thallium\",bis(methanaminium) bismuth thallium bromide,3,bulk polycrystalline,,,,,,,,\"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide (MA)Br\",red octahedral single crystals,\"TlBr was prepared in lab by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. This resulted in clear, colorless solutions. Next, the (TBA)Br solution was added to the Tl(PF6) solution dropwise and under constant stirring. TlBr resulted as a yellow, solid precipitate and was filtered, washed with MeCN, and added to 1 mL of concentrated HBr, which contained BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The solution was sonicated for 5 minutes, resulting in an orange-red solid that transformed into a deep red. After one hour, the solid was isolated via filtration, residual solvent was removed, and 298 mg of solid yielded. The crystals sat, undisturbed, for 1 week at room temperature. The polycrystalline powder was coated on a glass slide with grease, mounted in the integrating sphere, and measured with a Cary 6000i spectrometer in reflectance mode.\",UV-vis absorption,Solid-state reflectance spectra were collected via a Cary 6000i spectrometer and converted to pseudo-absorbance spectra using the Kubelka-Munk transformation. Band gaps were extracted by fitting linear regions of the Tauc plot (indirect formalism).\r\n10.1021/jacs.7b01629,Bis(methylammonium) thallium bismuth bromide,C2H12N2BiBr6Tl,\"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",CH6N,\"TlBiBr6, Bismuth bromide thallium\",bis(methanaminium) bismuth thallium bromide,3,single crystal,VASP,DFT,PBE+SOC,,,PAW,,,,,,\r\n10.1021/jacs.7b01629,Bis(methylammonium) thallium bismuth bromide,C2H12N2BiBr6Tl,\"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",CH6N,\"TlBiBr6, Bismuth bromide thallium\",bis(methanaminium) bismuth thallium bromide,3,single crystal,VASP,DFT,HSE06+SOC,6x6x6 Γ-centered k-point meshes,,PAW,,,,,,\r\n10.1021/jacs.7b01629,Bis(methylammonium) thallium bismuth bromide,C2H12N2BiBr6Tl,\"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",CH6N,\"TlBiBr6, Bismuth bromide thallium\",bis(methanaminium) bismuth thallium bromide,3,powder,,,,,,,,\"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide (MA)Br\",red octahedral single crystals,\"TlBr was first synthesized by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. Then, the (TBA)Br solution was added dropwise to the Tl(PF6) solution while being stirred, and TlBr precipitated. This precipitate was added to 1 mL of concentrated HBr with BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The mixture was soniated for 5 minutes and remained undisturbed for one hour to result in single crystals.\",X-ray absorption spectroscopy (XAS),\"Data were obtained at the Stanford Synchrotron Radiation Lightsource (SSRL) with beamline 2-2 at room temperature. A Lytle fluorescence detector was used in transmission mode to measure the XAS data, using a selenium foil for reference. The inflection point on the selenium rising edge was fixed at 12658 eV, and the spectra were normalized.\"\r\n10.1021/jacs.7b01629,Bis(methylammonium) thallium bismuth bromide,C2H12N2BiBr6Tl,\"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",CH6N,\"TlBiBr6, Bismuth bromide thallium\",bis(methanaminium) bismuth thallium bromide,3,single crystal,,,,,,,,\"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide (MA)Br\",red octahedral single crystals,\"TlBr was first synthesized by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. Then, the (TBA)Br solution was added dropwise to the Tl(PF6) solution while being stirred, and TlBr precipitated. This precipitate was added to 1 mL of concentrated HBr with BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The mixture was soniated for 5 minutes and remained undisturbed for one hour to result in single crystals.\",Raman microscopy,The spectrum was recorded using a Renishaw RM1000 Raman microscope\r\n10.1021/jacs.7b06143,Tetra(ethylammonium) lead bromide,C8H32N4Pb3Br10,\"tetra(ethanaminium) decabromo triplumbate(II), EA4Pb3Br10, (CH3CH2NH3)4Pb3Br10, (C2H8N)4Pb3Br10\",C2H8N,\"Pb3Br10, Lead bromide\",tetra(ethanaminium) lead(II) bromide,2,single crystal,,,,,,,,\"PbO (99.9%), PbBr2 (98%), ethylamine hydrochloride (98%), and hydrobromic acid ( 48%)\",Yellow rectangular plate-like crystals of (CH3CH2NH3)4Pb3Br10 [Yield: 53.3% w.r.t. Pb],\"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 10 mL of 48% hydrobromic acid at 180 °C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating. The solution was slowly cooled to room temperature.\",Diffuse reflectance,\"Spectra were collected using a Shimadzu UV-3600 UV−vis− NIR spectrometer operating in the 200−1000 nm region using BaSO4 as the reference of 100% reflectance. The reflectance was converted to absorption according to the Kubelka−Munk equation: α/S =(1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.7b06143,Tetra(ethylammonium) lead bromide,C8H32N4Pb3Br10,\"tetra(ethanaminium) decabromo triplumbate(II), EA4Pb3Br10, (CH3CH2NH3)4Pb3Br10, (C2H8N)4Pb3Br10\",C2H8N,\"Pb3Br10, Lead bromide\",tetra(ethanaminium) lead(II) bromide,2,single crystal,,,,,,,,\"PbO (99.9%), PbBr2 (98%), ethylamine hydrochloride (98%), and hydrobromic acid ( 48%)\",Yellow rectangular plate-like crystals of (CH3CH2NH3)4Pb3Br10 [Yield: 53.3% w.r.t. Pb],\"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 10 mL of 48% hydrobromic acid at 180 °C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating. The solution was slowly cooled to room temperature.\",Single crystal X-ray diffraction,Frames were collected using an STOE IPDS 2 or IPDS 2T diffractometer with graphite monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2. Integration and numerical absorption corrections were done using the STOE X-AREA programs.\r\n10.1021/jacs.7b06143,Tetra(ethylammonium) lead chloride,C8H32N4Pb3Cl10,\"tetra(ethanaminium) decachloro triplumbate(II), EA4Pb3Cl10, (CH3CH2NH3)4Pb3Cl10, (C2H8N)4Pb3Cl10\",C2H8N,\"Pb3Cl10, Lead chloride\",tetra(ethanaminium) lead(II) chloride,2,single crystal,,,,,,,,\"PbO (99.9%), PbCl2 (98%), ethylamine hydrochloride (98%), hydrochloric acid (ACS reagent, 37%)\",Transparent rectangular plate-like crystals of (CH3CH2NH3)4Pb3Cl10 [Yield: 53.3% w.r.t. Pb],\"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 20 mL of 37% hydrochloric acid at 180 °C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating until about 70% of the above solution was evaporated. The solution was slowly cooled to room temperature.\",Diffuse reflectance,\"Spectra were collected using a Shimadzu UV-3600 UV−vis− NIR spectrometer operating in the 200−1000 nm region using BaSO4 as the reference of 100% reflectance. The reflectance was converted to absorption according to the Kubelka−Munk equation: α/S =(1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.7b06143,Tetra(ethylammonium) lead chloride,C8H32N4Pb3Cl10,\"tetra(ethanaminium) decachloro triplumbate(II), EA4Pb3Cl10, (CH3CH2NH3)4Pb3Cl10, (C2H8N)4Pb3Cl10\",C2H8N,\"Pb3Cl10, Lead chloride\",tetra(ethanaminium) lead(II) chloride,2,single crystal,,,,,,,,\"PbO (99.9%), PbCl2 (98%), ethylamine hydrochloride (98%), hydrochloric acid (ACS reagent, 37%)\",Transparent rectangular plate-like crystals of (CH3CH2NH3)4Pb3Cl10 [Yield: 53.3% w.r.t. Pb],\"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 20 mL of 37% hydrochloric acid at 180 °C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating until about 70% of the above solution was evaporated. The solution was slowly cooled to room temperature.\",Single crystal X-ray diffraction,Frames were collected using an STOE IPDS 2 or IPDS 2T diffractometer with graphite monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2. Integration and numerical absorption corrections were done using the STOE X-AREA programs.\r\n10.1021/jacs.7b09096,Guanidinium methylammonium lead iodide,(C(NH2)3)(CH3NH3)PbI4,\"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\"CH6N3, CH6N\",\"PbI4, Lead iodide\",diaminomethanaminium methanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Red needle-like crystals,\"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until ∼25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Single-crystal X-ray diffraction,\"SCXRD was performed with a STOE IPDS II or IPDS 2T diffractometer using Mo Kalpha radiation working at 50 kV and 40 mA. Integration and absorption corrections were made with the X-AREA, X-RED, and X-SHAPE programs. Structures were solved via charge flipping and were refined full-matrix least squares with the Jana2006 package. PLATON software was used to identify twinning domains and to validate the space groups.\"\r\n10.1021/jacs.7b09096,Guanidinium methylammonium lead iodide,(C(NH2)3)(CH3NH3)PbI4,\"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\"CH6N3, CH6N\",\"PbI4, Lead iodide\",diaminomethanaminium methanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Red needle-like crystals,\"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until ∼25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transformation was used to convert the data to absorbance.\"\r\n10.1021/jacs.7b09096,Guanidinium methylammonium lead iodide,(C(NH2)3)(CH3NH3)PbI4,\"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\"CH6N3, CH6N\",\"PbI4, Lead iodide\",diaminomethanaminium methanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Red needle-like crystals,\"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until ∼25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Photoluminescence Spectra,\"A Horiba LabRam Evolution high-res confocal Ramon microscope spectrometer that was equipped with a diode CW laser (excitation wavelength 473 nm, 25 mW power) and a Synapse CCD camera was used. PL spectra were measured on the oriented crystals.\"\r\n10.1021/jacs.7b09096,Guanidinium methylammonium lead iodide,(C(NH2)3)(CH3NH3)PbI4,\"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\"CH6N3, CH6N\",\"PbI4, Lead iodide\",diaminomethanaminium methanaminium lead (II) iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Red needle-like crystals,\"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until ∼25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BaSO4 was used as the 100% reflectance reference, and the Kubelka-Munk transformation was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\"\r\n10.1021/jacs.7b09096,Guanidinium bis(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)2Pb2I7,\"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\"CH6N3, CH6N\",\"Pb2I7, Lead iodide\",diaminomethanaminium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Dark red single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Single-crystal X-ray diffraction,\"SCXRD was performed with a STOE IPDS II or IPDS 2T diffractometer using Mo Kalpha radiation working at 50 kV and 40 mA. Integration and absorption corrections were made with the X-AREA, X-RED, and X-SHAPE programs. Structures were solved via charge flipping and were refined full-matrix least squares with the Jana2006 package. PLATON software was used to identify twinning domains and to validate the space groups.\"\r\n10.1021/jacs.7b09096,Guanidinium bis(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)2Pb2I7,\"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\"CH6N3, CH6N\",\"Pb2I7, Lead iodide\",diaminomethanaminium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Dark red single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\"\r\n10.1021/jacs.7b09096,Guanidinium bis(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)2Pb2I7,\"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\"CH6N3, CH6N\",\"Pb2I7, Lead iodide\",diaminomethanaminium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Dark red single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Photoluminescence Spectra,\"A Horiba LabRam Evolution high-res confocal Ramon microscope spectrometer that was equipped with a diode CW laser (excitation wavelength 473 nm, 25 mW power) and a Synapse CCD camera was used. PL spectra were measured on the oriented crystals.\"\r\n10.1021/jacs.7b09096,Guanidinium bis(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)2Pb2I7,\"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\"CH6N3, CH6N\",\"Pb2I7, Lead iodide\",diaminomethanaminium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Dark red single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\"\r\n10.1021/jacs.7b09096,Guanidinium tris(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)3Pb3I10,\"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\"CH6N3, CH6N\",\"Pb3I10, Lead iodide\",diaminomethanaminium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Black single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Single-crystal X-ray diffraction,\"SCXRD was performed with a STOE IPDS II or IPDS 2T diffractometer using Mo Kalpha radiation working at 50 kV and 40 mA. Integration and absorption corrections were made with the X-AREA, X-RED, and X-SHAPE programs. Structures were solved via charge flipping and were refined full-matrix least squares with the Jana2006 package. PLATON software was used to identify twinning domains and to validate the space groups.\"\r\n10.1021/jacs.7b09096,Guanidinium tris(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)3Pb3I10,\"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\"CH6N3, CH6N\",\"Pb3I10, Lead iodide\",diaminomethanaminium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Black single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\"\r\n10.1021/jacs.7b09096,Guanidinium tris(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)3Pb3I10,\"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\"CH6N3, CH6N\",\"Pb3I10, Lead iodide\",diaminomethanaminium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Black single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Photoluminescence,\"A Horiba LabRam Evolution high-res confocal Ramon microscope spectrometer that was equipped with a diode CW laser (excitation wavelength 473 nm, 25 mW power) and a Synapse CCD camera was used. PL spectra were measured on the oriented crystals.\"\r\n10.1021/jacs.7b09096,Guanidinium tris(methylammonium) lead iodide,(C(NH2)3)(CH3NH3)3Pb3I10,\"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\"CH6N3, CH6N\",\"Pb3I10, Lead iodide\",diaminomethanaminium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, ≥98%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",Black single crystals,\"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\"\r\n10.1021/jacs.7b09417,Guanidinium hypophosphite,C2H24Mn2N6O12P6,[GUA]Mn(H2POO)3,CH6N3,Mn(H2POO)3,diaminomethanaminium hypophosphite,3,single crystal,,,,,,,,\"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco.\",[GUA]Mn(H2POO)3,\"The solutions of manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution and the addition of alkylamine and alkylammonium dissolved into vapor diffusions provided pure samples of GUA and FA phases. In the acetone vapor-diffusion vial, single crystals of the monoclinic phase of [GUA]Mn(H2POO3) were produced as well as the triclinic phase of the compound from the DMSO vapor-diffusion. Although both phases crystallized, the sample was converted to the pure monoclinic phase via heating at 130 °C for 2 hours.\",Quantum Design Magnetic Properties Measurement System (MPMS3),\"The magnetic susceptibility measurements of [GUA]Mn(H2POO)3 were calculated using MPMS3 and SQUID. [GUA]Mn(H2POO)3 was cooled to 1000 Oe in zero field mode. Since the temperature range was set to 2 to 300 K, only [GUA]Mn(H2POO)3 showed antiferromagnetic behavior, which gave a Neel temperature of 6.5K. The Curie-Weiss law was used to as a graphing technique to obtain the Weiss constants of both compounds. The Weiss constant of [GUA]Mn(H2POO)3 was measured to be -9.868 K with an effective magnetic moment of 6.12.\"\r\n10.1021/jacs.7b09417,Formamidinium hypophosphite,CH12MnN2O6P3,[FA]Mn(H2POO)3,CH5N2,Mn(H2POO)3,diaminomethanide hypophosphite,3,single crystal,,,,,,,,\"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco\",[FA]Mn(H2POO)3,\"The solutions of manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution and the addition of alkylamine and alkylammonium dissolved into vapor diffusions provided pure samples of FA phases. Although both phases crystallized, the sample was converted to the pure monoclinic phase via heating at 130 °C for 2 hours. The phase pure samples of [FA]Mn(H2POO3) were produced from the DMF vapor diffusion.\",Quantum Design Magnetic Properties Measurement System (MPMS3),he magnetic susceptibility measurements of [FA]Mn(H2POO3) were calculated using MPMS3 and SQUID. [FA]Mn(H2POO3) was cooled to 100 Oe in zero fields. The Curie-Weiss law was used to as a graphing technique to obtain the Weiss constants of both compounds. The Weiss constant of [FA]Mn(H2POO3) was found to be -5.766 K with an effective magnetic momentum of 5.02.\r\n10.1021/jacs.7b09417,Guanidinium hypophosphite,C2H24Mn2N6O12P6,[GUA]Mn(H2POO)3,CH6N3,Mn(H2POO)3,diaminomethanaminium hypophosphite,3,single crystal,,,,,,,,,,,,\r\n10.1021/jacs.7b09417,Guanidinium hypophosphite,C2H24Mn2N6O12P6,[GUA]Mn(H2POO)3,CH6N3,Mn(H2POO)3,diaminomethanaminium hypophosphite,3,single crystal,,,,,,,,,,,,\r\n10.1021/jacs.7b09417,Formamidinium hypophosphite,CH12MnN2O6P3,[FA]Mn(H2POO)3,CH5N2,Mn(H2POO)3,diaminomethanide hypophosphite,3,single crystal,,,,,,,,,,,,\r\n10.1021/jacs.7b09417,Formamidinium hypophosphite,CH12MnN2O6P3,[FA]Mn(H2POO)3,CH5N2,Mn(H2POO)3,diaminomethanide hypophosphite,3,single crystal,,,,,,,,,,,,\r\n10.1021/jacs.7b09417,Guanidinium hypophosphite,C2H24Mn2N6O12P6,[GUA]Mn(H2POO)3,CH6N3,Mn(H2POO)3,diaminomethanaminium hypophosphite,3,powder,VASP,DFT,PBE,2×2×2,non-collinear magnetism,PAW (projector augmented wave) pseudopotentials and the wavefunction is expanded with a plane-wave basis set,+17 meV,\"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco.\",[GUA]Mn(H2POO)3,\"ath sonication and magnetic stirring/heating at 50°C was used to dissolved manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution (50% w/w; o.646 mL, 6 mmol). Then, alkylamine and alkylammonium sat (1 mmol) was added to the solution and stirred until it was dissolved. After dividing the solutions into 6 samples, each was dropped into various vapor diffusions that contained acetone, ethanol, N, N-dimethylacetamide (DMAC), N, N-dimethylformamide (DMF), or dimethyl sulfoxide (DMSO). Crystals were then obtained as acetone and ethanol diffused into the reactions, reducing the solubility of the solution as well as water increasing the concentration of the solvents at room temperature. The crystals observed were either colorless and small, indicating all phases present, or large with a pink color.\",TGA/DSC analysis,An SDT instrument (simultaneous differential scanning calorimetry - thermogravimetric analysis (TGA)) was used to analyze the thermal stability of f [GUA]Mn(H2POO)3 and [FA]Mn(H2POO)3. These powder samples were heated to 600°C at 20°C/min under an argon flow of 100 ml/min.\r\n10.1021/jacs.7b09417,Formamidinium hypophosphite,CH12MnN2O6P3,[FA]Mn(H2POO)3,CH5N2,Mn(H2POO)3,diaminomethanide hypophosphite,3,powder,,,,,,,,\"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco.\",[FA]Mn(H2POO)3,\"Bath sonication and magnetic stirring/heating at 50°C was used to dissolved manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution (50% w/w; o.646 mL, 6 mmol). Then, alkylamine and alkylammonium sat (1 mmol) was added to the solution and stirred until it was dissolved. After dividing the solutions into 6 samples, each was dropped into various vapor diffusions that contained acetone, ethanol, N, N-dimethylacetamide (DMAC), N, N-dimethylformamide (DMF), or dimethyl sulfoxide (DMSO). Crystals were then obtained as acetone and ethanol diffused into the reactions, reducing the solubility of the solution as well as water increasing the concentration of the solvents at room temperature. The crystals observed were either colorless and small, indicating all phases present, or large with a pink color.\",TGA/DSC analysis,An SDT instrument (simultaneous differential scanning calorimetry - thermogravimetric analysis (TGA)) was used to analyze the thermal stability of f [GUA]Mn(H2POO)3 and [FA]Mn(H2POO)3. These powder samples were heated to 600°C at 20°C/min under an argon flow of 100 ml/min.\r\n10.1021/jacs.7b10223,Bis(hexylammonium) lead iodide,C12H32N2PbI4,\"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",C6H16N,\"PbI4, Lead iodide\",bis(hexyl-1-aminium) lead(II) iodide,2,powder,,,,,,,,\"HI, HA (C6H13NH3), Et2O, PbI2\",Powder of (C6H13NH3)2PbI4,\"Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). To prepare powder for XRD, drop-cast thin film from 200 mg/mL solutions and anneal at 70 °C for 15 min.\",Powder X-ray diffraction,\"Bruker X-ray D8 Advance diffractometer with Cu Kα1,2 radiation (λ = 1.541 Å). Spectra were collected with an angular range of 5 < 2θ < 60° and step size of 0.01022 ° over 60 minutes. Rietveld analysis was carried out using the TOPAS program. Low-temperature measurements were made on cooling between 300−12K using an Oxford Cyrosytem PheniX stage.\"\r\n10.1021/jacs.7b10223,Bis(dodecylammonium) lead iodide,C24H56N2PbI4,\"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",C12H28N,\"PbI4, Lead iodide\",bis(dodecyl-1-aminium) lead(II) iodide,2,powder,,,,,,,,\"HI, DA (C12H25NH3), Et2O, PbI2\",Powder of (C12H25NH3)2PbI4,\"Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). To prepare powder for XRD, drop-cast thin film from 200 mg/mL solutions and anneal at 70 °C for 15 min.\",Powder X-ray diffraction,\"Bruker X-ray D8 Advance diffractometer with Cu Kα1,2 radiation (λ = 1.541 Å). Spectra were collected with an angular range of 5 < 2θ < 60° and step size of 0.01022° over 60 minutes. Rietveld analysis was carried out using the TOPAS program. Low-temperature\r\nmeasurements were made on cooling between 300−12K using an Oxford Cyrosytem PheniX stage.\"\r\n10.1021/jacs.7b10223,Bis(dodecylammonium) lead iodide,C24H56N2PbI4,\"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",C12H28N,\"PbI4, Lead iodide\",bis(dodecyl-1-aminium) lead(II) iodide,2,film,,,,,,,,\"HI, DA (C12H25NH3), Et2O, PbI2\",Thin film of (C12H25NH3)2PbI4,Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 °C.,Photoluminescence spectra,Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\r\n10.1021/jacs.7b10223,Bis(hexylammonium) lead iodide,C12H32N2PbI4,\"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",C6H16N,\"PbI4, Lead iodide\",bis(hexyl-1-aminium) lead(II) iodide,2,film,,,,,,,,\"HI, HA (C6H13NH3), Et2O, PbI2\",Thin film of (C6H13NH3)2PbI4,Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 °C.,Photoluminescence spectra,Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\r\n10.1021/jacs.7b10223,Bis(hexylammonium) lead iodide,C12H32N2PbI4,\"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",C6H16N,\"PbI4, Lead iodide\",bis(hexyl-1-aminium) lead(II) iodide,2,powder,,,,,,,,\"C6H16N, HI, PbI2, EtO2\",Powder of (C6H13NH3)2PbI4,Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 °C.,Photoluminescence spectra,Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\r\n10.1021/jacs.7b10223,Bis(dodecylammonium) lead iodide,C24H56N2PbI4,\"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",C12H28N,\"PbI4, Lead iodide\",bis(dodecyl-1-aminium) lead(II) iodide,2,film,,,,,,,,\"HI, DA (C12H25NH3), Et2O, PbI2\",Thin film of (C12H25NH3)2PbI4,Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 °C.,Photoluminescence spectra,Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\r\n10.1021/jacs.7b10223,Bis(hexylammonium) lead iodide,C12H32N2PbI4,\"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",C6H16N,\"PbI4, Lead iodide\",bis(hexyl-1-aminium) lead(II) iodide,2,film,,,,,,,,\"C6H16N, HI, PbI2, EtO2\",Thin film of (C12H25NH3)2PbI4,Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 °C.,UV-Vis absorption,Steady-state room-temperature absorption spectra were determined by placing spin-coated films on glass in a using an HP 8453 spectrometer.\r\n10.1021/jacs.7b10223,Bis(dodecylammonium) lead iodide,C24H56N2PbI4,\"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",C12H28N,\"PbI4, Lead iodide\",bis(dodecyl-1-aminium) lead(II) iodide,2,film,,,,,,,,\"HI, DA (C12H25NH3), Et2O, PbI2\",Thin film of (C12H25NH3)2PbI4,Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 °C.,UV-Vis absorption,Steady-state room-temperature absorption spectra were determined by placing spin-coated films on glass in a using an HP 8453 spectrometer.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium lead iodide,C6H16N2PbI4,\"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",C6H16N2,\"PbI4, Lead iodide\",3-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (50 wt % in water)\",Red plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium lead iodide,C6H16N2PbI4,\"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",C6H16N2,\"PbI4, Lead iodide\",3-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single crystal X-ray diffraction,The data were collected using either an STOE IPDS 2 or an IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium lead iodide,C6H16N2PbI4,\"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",C6H16N2,\"PbI4, Lead iodide\",3-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium lead iodide,C6H16N2PbI4,\"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",C6H16N2,\"PbI4, Lead iodide\",3-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium lead iodide,C6H16N2PbI4,\"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",C6H16N2,\"PbI4, Lead iodide\",3-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium lead iodide,C6H16N2PbI4,\"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",C6H16N2,\"PbI4, Lead iodide\",3-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",3-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Dark red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single-crystal X-ray diffraction,The data were collected using a Bruker Molly instrument with MoKα IμS microfocus source (λ = 0.71073 Å) with MX Optics at 250 K.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",3-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Dark red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence Spectra,Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",3-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Dark red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",3-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Dark red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",3-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), methylammonium iodide (MAI), PbO, HI, H3PO2\",Dark red crystals,PbO powder was dissolved in a solution of HI and H3PO2 that was heated and stirred for 5-10 minutes at around 130 degrees Celsius. The solution became clear and bright yellow. Then MAI was added to the same solution while still being held at 130 degrees. HI was added to the organic cation (3AMP or 4AMP) in a separate vial under similar conditions. The molar ratio 4AMP:MAI:PbO was 0.5:2:3. The latter solution was then added to the former solution and heated/stirred at 240 degrees for 5 minutes. Slow cooling afterwards to room temperature caused crystals to precipitate.,Diffuse Reflectance Spectra,A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The band gaps of the systems were extrapolated after converting reflectance to absorption via the Kubelka-Munk relation.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium bis(methylammonium) lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",3-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single-crystal X-ray diffraction,The data were collected using a Bruker Molly instrument with MoKα IμS microfocus source (λ = 0.71073 Å) with MX Optics at 250 K.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium bis(methylammonium) lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",3-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium bis(methylammonium) lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",3-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium bis(methylammonium) lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",3-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium bis(methylammonium) lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",3-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium tris(methylammonium) lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",3-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single crystal X-ray diffraction,The data were collected using either an STOE IPDS 2 or an IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium tris(methylammonium) lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",3-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium tris(methylammonium) lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",3-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium tris(methylammonium) lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",3-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium tris(methylammonium) lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",3-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium lead iodide,(C6H16N2)PbI4,\"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Orange plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single-crystal X-ray diffraction,The data were collected using either an STOE IPDS 2 or an IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium lead iodide,(C6H16N2)PbI4,\"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Orange plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium lead iodide,(C6H16N2)PbI4,\"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Orange plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium lead iodide,(C6H16N2)PbI4,\"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Orange plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium lead iodide,(C6H16N2)PbI4,\"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Orange plate-like crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 °C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",4-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single-crystal X-ray diffraction,The data were collected using a Bruker Molly instrument with MoKα IμS microfocus source (λ = 0.71073 Å) with MX Optics at 250 K.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",4-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",4-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",4-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",4-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium bis(methylammonium lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",4-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single-crystal X-ray diffraction,The data were collected using a Bruker Molly instrument with MoKα IμS microfocus source (λ = 0.71073 Å) with MX Optics at 250 K.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium bis(methylammonium lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",4-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium bis(methylammonium lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",4-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium bis(methylammonium lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",4-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium bis(methylammonium lead iodide,(C6H16N2)(CH3NH3)2Pb3I10,\"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H16N2, CH6N\",\"Pb3I10, Lead iodide\",4-(methanaminium)piperidinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium tris(methylammonium lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",4-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Single-crystal X-ray diffraction,The data were collected using a Bruker Molly instrument with MoKα IμS microfocus source (λ = 0.71073 Å) with MX Optics at 250 K.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium tris(methylammonium lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",4-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium tris(methylammonium lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",4-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Photoluminescence,A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium tris(methylammonium lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",4-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\n10.1021/jacs.8b00542,4-(aminomethyl)piperidinium tris(methylammonium lead iodide,(C6H16N2)(CH3NH3)3Pb4I13,\"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H16N2, CH6N\",\"Pb4I13, Lead iodide\",4-(methanaminium)piperidinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Black crystals,\"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b00542,3-(aminomethyl)piperidinium methylammonium lead iodide,(C6H16N2)(CH3NH3)Pb2I7,\"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\"C6H16N2, CH6N\",\"Pb2I7, Lead iodide\",3-(methanaminium)piperidinium methanaminium lead iodide,2,single crystal,,,,,,,,\"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",Dark red crystals,\"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5−10 min at ∼130 °C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",Diffuse Reflectance Spectra,\"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka−Munk equation: α/S = (1 − R)^2/(2R), where R is the reflectance and α and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\"\r\n10.1021/jacs.8b03659,Bis(naphthaleneoxyethylammonium) lead iodide,\"(C12H14ON)2PbI4, C24H28O2N2PbI4\",\"(Nap-O-Et-NH3)2PbI4, (naphthalene-O-ethyl-NH3)2PbI4, bis(naphthaleneoxyethylaminium) tetraiodoplumbate(II)\",C12H14ON,\"PbI4, Lead iodide\",bis(naphthaleneoxyethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane, γ-butyrolactone (GBL), naphthaleneoxyethylammonium iodide , lead iodide\",Orange plate-like crystals,\"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(naphthaleneoxypropylammonium) lead iodide,(C13H16ON)2PbI4,\"(Nap-O-Pr-NH3)2PbI4, (naphthalene-O-propyl-NH3)2PbI4, bis(naphthaleneoxypropylaminium) tetraiodoplumbate(II)\",C13H16ON,\"PbI4, Lead iodide\",bis(naphthaleneoxypropylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane, γ-butyrolactone (GBL), naphthaleneoxypropylammonium iodide, lead iodide\",Yellow plate-like crystals,\"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(naphthaleneoxypropylammonium) lead iodide·γ-butyrolactone,\"(C4H6O2)0.5(C13H16ON)2PbI4, C28H35O3N2PbI4\",\"(Nap-O-Pr-NH3)2PbI4¬∑(C4H6O2)0.5, bis(naphthalene-O-propyl-NH3) tetraiodoplumbate(II)\",\"C4H6O2,C13H16ON\",\"PbI4, Lead iodide\",Bis(naphthaleneoxypropylammonium) lead (II) iodide·γ-butyrolactone,2,single crystal,,,,,,,,\"Dichloromethane, γ-butyrolactone (GBL), naphthaleneoxypropylammonium iodide, lead iodide\",Orange plate-like crystals,\"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(pyreneoxyethylammonium) lead iodide,\"(C18H16ON)2PbI4, C36H32O2N2PbI4\",\"(pyrene-O-ethyl-NH3)2PbI4, bis(pyreneoxyethylaminium) tetraiodoplumbate(II)\",C18H16ON,\"PbI4, Lead iodide\",bis(pyreneoxyethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane, γ-butyrolactone (GBL), pyreneoxyethylammonium iodide, lead iodide\",Orange plate-like crystals,\"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(pyreneoxypropylammonium) lead iodide,(C19H18ON)2PbI4,\"(pyrene-O-propyl-NH3)2PbI4, bis(pyreneoxypropylaminium) tetraiodoplumbate(II)\",C19H18ON,\"PbI4, Lead iodide\",bis(pyreneoxypropylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane, γ-butyrolactone (GBL), pyreneoxypropylammonium iodide, lead iodide\",Red plate-like crystals,\"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(pyreneoxybutylammonium) lead iodide,(C20H20ON)2PbI4,\"(pyrene-O-butyl-NH3)2PbI4, bis(pyreneoxybutylaminium) tetraiodoplumbate(II)\",C20H20ON,\"PbI4, Lead iodide\",bis(pyreneoxybutylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane, γ-butyrolactone (GBL), pyreneoxybutylammonium iodide, lead iodide\",Orange plate-like crystals,\"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(perylenoxyethylammonium) lead iodide,(C22H18ON)2PbI4,\"(perylene-O-ethyl-NH3)2PbI4, bis(perylenoxyethylaminium) tetraiodoplumbate(II)\",C22H18ON,\"PbI4, Lead iodide\",bis(perylenoxyethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane, γ-butyrolactone (GBL), perylenoxyethylammonium iodide, lead iodide\",Orange plate-like crystals,\"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(naphthaleneoxyethylammonium) lead iodide,\"(C12H14ON)2PbI4, C24H28O2N2PbI4\",\"(Nap-O-Et-NH3)2PbI4, (naphthalene-O-ethyl-NH3)2PbI4, bis(naphthaleneoxyethylaminium) tetraiodoplumbate(II)\",C12H14ON,\"PbI4, Lead iodide\",bis(naphthaleneoxyethylaminium) lead (II) iodide,2,film,,,,,,,,\"naphthaleneoxyethylammonium iodide salt, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\r\n10.1021/jacs.8b03659,Bis(naphthaleneoxypropylammonium) lead iodide,(C13H16ON)2PbI4,\"(Nap-O-Pr-NH3)2PbI4, (naphthalene-O-propyl-NH3)2PbI4, bis(naphthaleneoxypropylaminium) tetraiodoplumbate(II)\",C13H16ON,\"PbI4, Lead iodide\",bis(naphthaleneoxypropylaminium) lead (II) iodide,2,film,,,,,,,,\"naphthaleneoxypropylammonium iodide, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\r\n10.1021/jacs.8b03659,Bis(pyreneoxyethylammonium) lead iodide,\"(C18H16ON)2PbI4, C36H32O2N2PbI4\",\"(pyrene-O-ethyl-NH3)2PbI4, bis(pyreneoxyethylaminium) tetraiodoplumbate(II)\",C18H16ON,\"PbI4, Lead iodide\",bis(pyreneoxyethylaminium) lead (II) iodide,2,film,,,,,,,,\"pyreneoxyethylammonium iodide, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\r\n10.1021/jacs.8b03659,Bis(pyreneoxypropylammonium) lead iodide,(C19H18ON)2PbI4,\"(pyrene-O-propyl-NH3)2PbI4, bis(pyreneoxypropylaminium) tetraiodoplumbate(II)\",C19H18ON,\"PbI4, Lead iodide\",bis(pyreneoxypropylaminium) lead (II) iodide,2,film,,,,,,,,\"pyreneoxypropylammonium iodide, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\r\n10.1021/jacs.8b03659,Bis(pyreneoxybutylammonium) lead iodide,(C20H20ON)2PbI4,\"(pyrene-O-butyl-NH3)2PbI4, bis(pyreneoxybutylaminium) tetraiodoplumbate(II)\",C20H20ON,\"PbI4, Lead iodide\",bis(pyreneoxybutylaminium) lead (II) iodide,2,film,,,,,,,,\"pyreneoxybutylammonium iodide, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",UV-vis absorption,\"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\"\r\n10.1021/jacs.8b03659,Bis(perylenoxyethylammonium) lead iodide,(C22H18ON)2PbI4,\"(perylene-O-ethyl-NH3)2PbI4, bis(perylenoxyethylaminium) tetraiodoplumbate(II)\",C22H18ON,\"PbI4, Lead iodide\",bis(perylenoxyethylaminium) lead (II) iodide,2,film,,,,,,,,\"perylenoxyethylammonium iodide, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\r\n10.1021/jacs.8b03659,Bis(naphthaleneoxyethylammonium) lead iodide,\"(C12H14ON)2PbI4, C24H28O2N2PbI4\",\"(Nap-O-Et-NH3)2PbI4, (naphthalene-O-ethyl-NH3)2PbI4, bis(naphthaleneoxyethylaminium) tetraiodoplumbate(II)\",C12H14ON,\"PbI4, Lead iodide\",bis(naphthaleneoxyethylaminium) lead (II) iodide,2,film,,,,,,,,\"naphthaleneoxyethylammonium iodide, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",Photoluminescence,A Horiba Nanolog Fluorimeter instrument was used to measure the steady-state PL spectra.\r\n10.1021/jacs.8b03659,Bis(naphthaleneoxypropylammonium) lead iodide,(C13H16ON)2PbI4,\"(Nap-O-Pr-NH3)2PbI4, (naphthalene-O-propyl-NH3)2PbI4, bis(naphthaleneoxypropylaminium) tetraiodoplumbate(II)\",C13H16ON,\"PbI4, Lead iodide\",bis(naphthaleneoxypropylaminium) lead (II) iodide,2,film,,,,,,,,\"naphthaleneoxypropylammonium iodide, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",Photoluminescence,A Horiba Nanolog Fluorimeter instrument was used to measure the steady-state PL spectra.\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,single crystal,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",yellow crystals,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",single crystal X-ray diffraction,\"SuperNova diffractometer with Mo Kα radiation was used. Data was processed with Crystalclear software package, and the structures were solved by direct methods and refined with the SHELXLTL software package.\"\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,single crystal,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",yellow crystals,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",single crystal X-ray diffraction,\"SuperNova diffractometer with Mo Kα radiation was used. Data was processed with Crystalclear software package, and the structures were solved by direct methods and refined with the SHELXLTL software package.\"\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,single crystal,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",yellow crystals,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",Two-photon Absorption Coefficient Measurements,Z-scan apparatus was used to measure two-photon absorption property. The measurement was conducted with 350 fs pulses with a mode-locked fiber laser operating at 1030 nm and pulse repetition rate of 100 Hz.\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,single crystal,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",yellow crystals,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",Dielectric measurements,Dielectric constants were obtained by using single crystal samples with silver conducting paste. Analyses were performed with TongHui TH2828 analyzer between 300-350 K.\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,film,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",Film of thickness ~366 nm,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\r\n\r\nFilms were prepared by dissolving as-synthesized crystals at 500 mg/mL in dimethylformamide. The solutions are then spun onto wafers at 2500 rpm for 45 s, dried, and annealed at 80º C for 15 min.\",UV-vis absorbance,\"Measured at room temperature. A PE Lambda 900 UV-Visible spectrophotometer was used, and fluorescence measurements were collected with Edinbergh Analytical instrument FLS920.\"\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,bulk polycrystalline,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",yellow crystals,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",Thermogravimetric analysis,\"Conducted with STA449C Thermal Analyzer, ranging from room temperature to 600º C.\"\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,film,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",Film of thickness ~366 nm,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed. \r\nFilms were prepared by dissolving as-synthesized crystals at 500 mg/mL in dimethylformamide. The solutions are then spun onto wafers at 2500 rpm for 45 s, dried, and annealed at 80º C for 15 min.\",Photoluminescence,Edinbergh Analytical instrument FLS920 was used to record the spectrum\r\n10.1021/jacs.8b04014,Bis(butylammonium) formamidinium lead bromide,(C4H9NH3)2(NH2CHNH2)Pb2Br7,\"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\"C4H12N, N2H5C\",\"Pb2Br7, Lead bromide\",bis(butylaminium) diaminomethanide lead bromide,2,film,,,,,,,,\"Pb(Ch3COO)2•3H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",Film of thickness ~366 nm,\"First, Pb(Ch3COO)2•3H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed. Films were prepared by dissolving as-synthesized crystals at 500 mg/mL in dimethylformamide. The solutions are then spun onto wafers at 2500 rpm for 45 s, dried, and annealed at 80º C for 15 min.\",Photoluminescence,Edinbergh Analytical instrument FLS920 was used to record the spectrum\r\n10.1021/jacs.8b07712,\"1,8-octyldiammonium methylammonium lead iodide\",C9H28N3Pb2I7,\"(NH3C8H16NH3)(MA)Pb2I7, 1,8-octanediaminium methanaminium septaiodo diplumbate(II)\",\"C8H22N2, CH6N\",\"Pb2I7, Lead iodide\",\"1,8-octanediaminium methanaminium lead iodide\",2,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,8-diaminooctane (98%) from Sigma-Aldrich\",red plate-shaped crystals,\"223.2 mg PbO and 33.75 mg CH3NH2·HCl were added into a mixture of 1.5 mL of HI solution and 0.3 mL of H3PO2 solution under boiling temperature and vigorous stirring. \r\nAfter obtaining a clear yellow solution, 120 mg NH3C8H16NH3I2  was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 °C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75°C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",Single-crystal X-ray diffraction,\"STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.710 73 Å) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\"\r\n10.1021/jacs.8b07712,\"1,8-octyldiammonium bis(methylammonium) lead iodide\",C10H34N4Pb3I10,\"(NH3C8H16NH3)(MA)2Pb3I10, 1,8-octanediaminium bis(methanaminium) decaiodo triplumbate(II)\",\"C8H22N2, CH6N\",\"Pb3I10, Lead iodide\",\"1,8-octanediaminium bis(methanaminium) lead iodide\",2,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,8-diaminooctane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",dark red plate-shaped crystals,\"334.8 mg PbO and 67.5 mg CH3NH2·HCl were added into a mixture of 2.5 mL of HI solution and 0.5 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 112 mg NH3C8H16NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 °C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75°C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",Single-crystal X-ray diffraction,\"STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.710 73 Å) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\"\r\n10.1021/jacs.8b07712,\"1,8-octyldiammonium tris(methylammonium) lead iodide\",C11H40N5Pb4I13,\"(NH3C8H16NH3)(MA)3Pb4I13, 1,8-octanediaminium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C8H22N2, CH6N\",\"Pb4I13, Lead iodide\",\"1,8-octanediaminium tris(methanaminium) lead iodide\",2,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,8-diaminooctane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",black plate-shaped crystals,\"446.4 mg PbO and 101.28 mg CH3NH2·HCl were added into a mixture of 4 mL of HI solution and 0.8 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 80 mg  NH3C8H16NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 °C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75°C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",Single-crystal X-ray diffraction,\"STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.710 73 Å) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\"\r\n10.1021/jacs.8b07712,\"1,9-nonyldiammonium lead iodide\",C9H24N6PbI4,\"(NH3C9H18NH3)PbI4, NH3C9H18NH3PbI4, 1,9-nonanediaminium tetraiodoplumbate(II)\",C9H24N6,\"PbI4, Lead iodide\",\"1,9-nonanediaminium lead (II) iodide\",2,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,9-diaminononane (98%), from Sigma-Aldrich.\",orange plate-shaped crystals,\"44.6 mg PbO was added into a mixture of 2 mL of HI solution and 0.4 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 82.8 mg  NH3C9H18NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 °C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75°C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",Single-crystal X-ray diffraction,\"STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.710 73 Å) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\"\r\n10.1021/jacs.8b07712,\"1,9-nonyldiammonium methylammonium lead iodide\",C10H30N7Pb2I7,\"(NH3C9H18NH3)(MA)Pb2I7, 1,9-nonanediaminium methanaminium septaiodo diplumbate(II)\",\"C9H24N6, CH6N\",\"Pb2I7, Lead iodide\",\"1,9-nonanediaminium methanaminium lead iodide\",2,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,9-diaminononane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",red plate-shaped crystals,\"223.2 mg PbO and 33.75 mg CH3NH2·HCl were added into a mixture of 2 mL of HI solution and 0.4 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 74.5 mg  NH3C9H18NH3I2  was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 °C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75°C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",Single-crystal X-ray diffraction,\"STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.710 73 Å) operating at 50 kV and 40 mA were used to collect single crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption. Jana 2006 package was used to reslove structure. PLATON44 was used to validate space groups and twinning domains of the compounds.\"\r\n10.1021/jacs.8b07712,\"1,9-nonyldiammonium bis(methylammonium) lead iodide\",C11H36N8Pb3I10,\"(NH3C9H18NH3)(MA)2Pb3I10, 1,9-nonanediaminium bis(methanaminium) decaiodo triplumbate(II)\",\"C9H24N6, CH6N\",\"Pb3I10, Lead iodide\",\"1,9-nonanediaminium bis(methanaminium) lead iodide\",2,single crystal,,,,,,,,\"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,9-diaminononane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",dark red plate-shaped crystals,\"334.8 mg PbO and 67.5 mg CH3NH2·HCl were added into a mixture of 3.5 mL of HI solution and 0.7 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 58 mg  NH3C9H18NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 °C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75°C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",Single-crystal X-ray diffraction,\"STOE IPDS II or IPDS 2T diffractometer with Mo Kα radiation (λ = 0.710 73 Å) operating at 50 kV and 40 mA were used to collect single crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption. Jana 2006 package was used to reslove structure. PLATON44 was used to validate space groups and twinning domains of the compounds.\"\r\n10.1021/jacs.8b08691,\"Tris(2,6-dimethylpiperazine) lead bromide\",C18H48N6Pb2Br10,\"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",C6H16N2,\"Pb2Br10, Lead bromide\",\"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",1,single crystal,,,,,,,,\"PbBr2(98%), 2,6-dimethylpiperazine (97%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 2,6-dimethylpiperazine (342 mg, 3 mmol). Add the protonated 2,6-dimethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Single-crystal X-ray diffraction,Data were collected using a Bruker DUO or Molly instrument with a Mo Kα IμS microfocus source (λ = 0.71073 Å) with MX Optics at 250 K. Post-processing using APEX3 software and OLEX2 program package.\r\n10.1021/jacs.8b08691,4-(aminomethyl)piperidine lead bromide,C6H16N2PbBr4,\"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",4-(methanaminium)piperidine lead (II) bromide,2,single crystal,,,,,,,,\"PbBr2(98%), 4-(aminomethyl)piperidine (96%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 3 mmol of 4-(aminomethyl)piperidine. Add the protonated 4-(aminomethyl)-piperidine solution into A under heating for 2 min and cool to room temperature.,Single-crystal X-ray diffraction,Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\r\n10.1021/jacs.8b08691,1-ethylpiperazine lead bromide,C6H16N2PbBr4,\"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",\"1-ethane-1,3-diazinanium lead (II) bromide\",2,single crystal,,,,,,,,\"PbBr2(98%), 1-ethylpiperazine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 1-ethylpiperazine (342 mg, 3 mmol). Add the protonated 1-ethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Single-crystal X-ray diffraction,Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\r\n10.1021/jacs.8b08691,Bis(1-methylpiperazine) lead bromide,C10H28N4Pb3Br10,\"bis(1-methane-1,3-diazinanium) decabromo triplumbate(II), (mpz)2Pb3Br10, (C5H14N2)2Pb3Br10\",C5H14N2,\"Pb3Br10, Lead bromide\",\"bis(1-methane-1,3-diazinanium) lead (II) bromide\",2,single crystal,,,,,,,,\"PbBr2(98%), 1-methylpiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 1-methylpiperazine (200 mg, 2 mmol). Add the protonated 1-methylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Single-crystal X-ray diffraction,Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\r\n10.1021/jacs.8b08691,Homopiperazine lead bromide,C5H14N2PbBr4,\"1,4-diazepanium tetrabromoplumbate(II), (hmp)PbBr4, (C5H14N2)PbBr4\",C5H14N2,\"PbBr4, Lead bromide\",\"1,4-diazepanium lead bromide\",3,single crystal,,,,,,,,\"PbBr2(98%), homopiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of homopiperazine (300 mg, 3 mmol). Add the protonated homopiperazine solution into A under heating for 2 min and cool to room temperature.\",Single-crystal X-ray diffraction,Data were collected using an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\r\n10.1021/jacs.8b08691,Hexamethylenimine lead bromide,C6H14NPbBr3,\"Hexamethylenimine tribromoplumbate(II), (hex)PbBr3, (C6H14N)PbBr3\",C6H14N,\"PbBr3, Lead bromide\",azepanium lead (II) bromide,1,single crystal,,,,,,,,\"PbBr2(98%), hexamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of hexamethylenimine (297 mg, 3 mmol). Add the protonated hexamethylenimine solution into A under heating for 2 min and cool to room temperature.\",Single-crystal X-ray diffraction,Data were collected using either Bruker DUO or Molly instrument with a Mo Kα IμS microfocus source (λ = 0.71073 Å) with MX Optics at 250 K. Post-processing using APEX3 software and OLEX2 program package.\r\n10.1021/jacs.8b08691,Heptamethylenimine lead bromide,C7H16NPbBr3,\"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",C7H16N,\"PbBr3, Lead bromide\",azocanium lead (II) bromide,1,single crystal,,,,,,,,\"PbBr2(98%), heptamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of heptamethylenimine (339 mg, 3 mmol). Add the protonated heptamethylenimine solution into A under heating for 2 min and cool to room temperature.\",Single-crystal X-ray diffraction,Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\r\n10.1021/jacs.8b08691,\"Tris(2,6-dimethylpiperazine) lead bromide\",C18H48N6Pb2Br10,\"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",C6H16N2,\"Pb2Br10, Lead bromide\",\"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",1,unknown,,,,,,,,\"PbBr2(98%), 2,6-dimethylpiperazine (97%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 2,6-dimethylpiperazine (342 mg, 3 mmol). Add the protonated 2,6-dimethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Diffuse reflectance spectroscopy,\"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV−vis−NIR spectrometer operating in the 200−1000 nm region. Convert reflectance to absorption according to the Kubelka−Munk equation to estimate the band gap.\"\r\n10.1021/jacs.8b08691,4-(aminomethyl)piperidine lead bromide,C6H16N2PbBr4,\"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",4-(methanaminium)piperidine lead (II) bromide,2,unknown,,,,,,,,\"PbBr2(98%), 4-(aminomethyl)piperidine (96%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 3 mmol of 4-(aminomethyl)piperidine. Add the protonated 4-(aminomethyl)-piperidine solution into A under heating for 2 min and cool to room temperature.,Diffuse reflectance spectroscopy,\"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV−vis−NIR spectrometer operating in the 200−1000 nm region. Convert reflectance to absorption according to the Kubelka−Munk equation to estimate the band gap.\"\r\n10.1021/jacs.8b08691,1-ethylpiperazine lead bromide,C6H16N2PbBr4,\"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",\"1-ethane-1,3-diazinanium lead (II) bromide\",2,unknown,,,,,,,,\"PbBr2(98%), 1-ethylpiperazine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 1-ethylpiperazine (342 mg, 3 mmol). Add the protonated 1-ethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Diffuse reflectance spectroscopy,\"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV−vis−NIR spectrometer operating in the 200−1000 nm region. Convert reflectance to absorption according to the Kubelka−Munk equation to estimate the band gap.\"\r\n10.1021/jacs.8b08691,Bis(1-methylpiperazine) lead bromide,C10H28N4Pb3Br10,\"bis(1-methane-1,3-diazinanium) decabromo triplumbate(II), (mpz)2Pb3Br10, (C5H14N2)2Pb3Br10\",C5H14N2,\"Pb3Br10, Lead bromide\",\"bis(1-methane-1,3-diazinanium) lead (II) bromide\",2,unknown,,,,,,,,\"PbBr2(98%), 1-methylpiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 1-methylpiperazine (200 mg, 2 mmol). Add the protonated 1-methylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Diffuse reflectance spectroscopy,\"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV−vis−NIR spectrometer operating in the 200−1000 nm region. Convert reflectance to absorption according to the Kubelka−Munk equation to estimate the band gap.\"\r\n10.1021/jacs.8b08691,Homopiperazine lead bromide,C5H14N2PbBr4,\"1,4-diazepanium tetrabromoplumbate(II), (hmp)PbBr4, (C5H14N2)PbBr4\",C5H14N2,\"PbBr4, Lead bromide\",\"1,4-diazepanium lead bromide\",3,unknown,,,,,,,,\"PbBr2(98%), homopiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of homopiperazine (300 mg, 3 mmol). Add the protonated homopiperazine solution into A under heating for 2 min and cool to room temperature.\",Diffuse reflectance spectroscopy,\"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV−vis−NIR spectrometer operating in the 200−1000 nm region. Convert reflectance to absorption according to the Kubelka−Munk equation to estimate the band gap.\"\r\n10.1021/jacs.8b08691,Hexamethylenimine lead bromide,C6H14NPbBr3,\"Hexamethylenimine tribromoplumbate(II), (hex)PbBr3, (C6H14N)PbBr3\",C6H14N,\"PbBr3, Lead bromide\",azepanium lead (II) bromide,1,unknown,,,,,,,,\"PbBr2(98%), hexamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of hexamethylenimine (297 mg, 3 mmol). Add the protonated hexamethylenimine solution into A under heating for 2 min and cool to room temperature.\",Diffuse reflectance spectroscopy,\"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV−vis−NIR spectrometer operating in the 200−1000 nm region. Convert reflectance to absorption according to the Kubelka−Munk equation to estimate the band gap.\"\r\n10.1021/jacs.8b08691,Heptamethylenimine lead bromide,C7H16NPbBr3,\"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",C7H16N,\"PbBr3, Lead bromide\",azocanium lead (II) bromide,1,unknown,,,,,,,,\"PbBr2(98%), heptamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of heptamethylenimine (339 mg, 3 mmol). Add the protonated heptamethylenimine solution into A under heating for 2 min and cool to room temperature.\",Diffuse reflectance spectroscopy,\"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV−vis−NIR spectrometer operating in the 200−1000 nm region. Convert reflectance to absorption according to the Kubelka−Munk equation to estimate the band gap.\"\r\n10.1021/jacs.8b08691,\"Tris(2,6-dimethylpiperazine) lead bromide\",C18H48N6Pb2Br10,\"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",C6H16N2,\"Pb2Br10, Lead bromide\",\"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",1,powder,,,,,,,,\"PbBr2(98%), 2,6-dimethylpiperazine (97%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 2,6-dimethylpiperazine (342 mg, 3 mmol). Add the protonated 2,6-dimethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Steady-state photoluminescence,\"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\"\r\n10.1021/jacs.8b08691,4-(aminomethyl)piperidine lead bromide,C6H16N2PbBr4,\"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",4-(methanaminium)piperidine lead (II) bromide,2,powder,,,,,,,,\"PbBr2(98%), 4-(aminomethyl)piperidine (96%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 3 mmol of 4-(aminomethyl)piperidine. Add the protonated 4-(aminomethyl)-piperidine solution into A under heating for 2 min and cool to room temperature.,Steady-state photoluminescence,\"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\"\r\n10.1021/jacs.8b08691,1-ethylpiperazine lead bromide,C6H16N2PbBr4,\"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",\"1-ethane-1,3-diazinanium lead (II) bromide\",2,powder,,,,,,,,\"PbBr2(98%), 1-ethylpiperazine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 1-ethylpiperazine (342 mg, 3 mmol). Add the protonated 1-ethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Steady-state photoluminescence,\"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\"\r\n10.1021/jacs.8b08691,Bis(1-methylpiperazine) lead bromide,C10H28N4Pb3Br10,\"bis(1-methane-1,3-diazinanium) decabromo triplumbate(II), (mpz)2Pb3Br10, (C5H14N2)2Pb3Br10\",C5H14N2,\"Pb3Br10, Lead bromide\",\"bis(1-methane-1,3-diazinanium) lead (II) bromide\",2,powder,,,,,,,,\"PbBr2(98%), 1-methylpiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of 1-methylpiperazine (200 mg, 2 mmol). Add the protonated 1-methylpiperazine solution into A under heating for 2 min and cool to room temperature.\",Steady-state photoluminescence,\"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\"\r\n10.1021/jacs.8b08691,Homopiperazine lead bromide,C5H14N2PbBr4,\"1,4-diazepanium tetrabromoplumbate(II), (hmp)PbBr4, (C5H14N2)PbBr4\",C5H14N2,\"PbBr4, Lead bromide\",\"1,4-diazepanium lead bromide\",3,powder,,,,,,,,\"PbBr2(98%), homopiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of homopiperazine (300 mg, 3 mmol). Add the protonated homopiperazine solution into A under heating for 2 min and cool to room temperature.\",Steady-state photoluminescence,\"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\"\r\n10.1021/jacs.8b08691,Hexamethylenimine lead bromide,C6H14NPbBr3,\"Hexamethylenimine tribromoplumbate(II), (hex)PbBr3, (C6H14N)PbBr3\",C6H14N,\"PbBr3, Lead bromide\",azepanium lead (II) bromide,1,powder,,,,,,,,\"PbBr2(98%), hexamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of hexamethylenimine (297 mg, 3 mmol). Add the protonated hexamethylenimine solution into A under heating for 2 min and cool to room temperature.\",Steady-state photoluminescence,\"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\"\r\n10.1021/jacs.8b08691,Heptamethylenimine lead bromide,C7H16NPbBr3,\"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",C7H16N,\"PbBr3, Lead bromide\",azocanium lead (II) bromide,1,powder,,,,,,,,\"PbBr2(98%), heptamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",Colorless crystals,\"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 °C (A). Add 1 mL of HBr into a separate vial of heptamethylenimine (339 mg, 3 mmol). Add the protonated heptamethylenimine solution into A under heating for 2 min and cool to room temperature.\",Steady-state photoluminescence,\"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\"\r\n10.1021/jacs.8b08691,\"Tris(2,6-dimethylpiperazine) lead bromide\",C18H48N6Pb2Br10,\"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",C6H16N2,\"Pb2Br10, Lead bromide\",\"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",1,single crystal,SIESTA package,DFT,revPBE-GGA,Energy cutoff of 150 Ry for real-space mesh size,\"SOC on-site approximation as proposed by Fernández-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier−Martins pseudopotentials,,,,,,\r\n10.1021/jacs.8b08691,4-(aminomethyl)piperidine lead bromide,C6H16N2PbBr4,\"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",4-(methanaminium)piperidine lead (II) bromide,2,single crystal,SIESTA package,DFT,revPBE-GGA,Energy cutoff of 150 Ry for real-space mesh size,\"SOC on-site approximation as proposed by Fernández-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier−Martins pseudopotentials,,,,,,\r\n10.1021/jacs.8b08691,1-ethylpiperazine lead bromide,C6H16N2PbBr4,\"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",C6H16N2,\"PbBr4, Lead bromide\",\"1-ethane-1,3-diazinanium lead (II) bromide\",2,single crystal,SIESTA package,DFT,revPBE-GGA,Energy cutoff of 150 Ry for real-space mesh size,\"SOC on-site approximation as proposed by Fernández-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier−Martins pseudopotentials,,,,,,\r\n10.1021/jacs.8b08691,Heptamethylenimine lead bromide,C7H16NPbBr3,\"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",C7H16N,\"PbBr3, Lead bromide\",azocanium lead (II) bromide,1,single crystal,SIESTA package,DFT,revPBE-GGA,Energy cutoff of 150 Ry for real-space mesh size,\"SOC on-site approximation as proposed by Fernández-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier−Martins pseudopotentials,,,,,,\r\n10.1021/jacs.8b12948,Bis(butylammonium) methylammonium lead bromide,[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7,\"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\"C4H12N, CNH6\",\"Pb2Br7, Lead bromide\",bis(butylaminium) methanaminium lead bromide,2,single crystal,,,,,,,,\"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",Yellow plate-shaped crystals,\"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous  HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",Single-Crystal X-ray diffraction,\"An Agilent Technologies SuperNova Dual Wavelength CCD diffractometer was used, and Mo-Kα radiation was performed. CrysAlisPro software was used for data reduction and absorption correction. Shelx software refined structures.\"\r\n10.1021/jacs.8b12948,Bis(butylammonium) methylammonium lead bromide,[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7,\"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\"C4H12N, CNH6\",\"Pb2Br7, Lead bromide\",bis(butylaminium) methanaminium lead bromide,2,single crystal,,,,,,,,\"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",Yellow plate-shaped crystals,\"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",Single-Crystal X-ray diffraction,\"An Agilent Technologies SuperNova Dual Wavelength CCD diffractometer was used, and Cu-Kα radiation was performed. CrysAlisPro software was used for data reduction and absorption correction. Shelx software refined structures.\"\r\n10.1021/jacs.8b12948,Bis(butylammonium) methylammonium lead bromide,[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7,\"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\"C4H12N, CNH6\",\"Pb2Br7, Lead bromide\",bis(butylaminium) methanaminium lead bromide,2,bulk polycrystalline,,,,,,,,\"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",Yellow plate-shaped crystals,\"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in aqueous  HBr solution (20 mL, 47%). These substances were dissolved through heating and boiling HBr, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved and a clear-yellow solution was resulted. Large crystals grew as the temperature cooled, and the crystals were elongated along crystallographic c-axis.\",UV-vis absorption,\r\n10.1021/jacs.8b12948,Bis(butylammonium) methylammonium lead bromide,[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7,\"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\"C4H12N, CNH6\",\"Pb2Br7, Lead bromide\",bis(butylaminium) methanaminium lead bromide,2,bulk polycrystalline,,,,,,,,\"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",Yellow plate-shaped crystals,\"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",,\r\n10.1021/jacs.8b12948,Bis(butylammonium) methylammonium lead bromide,[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7,\"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\"C4H12N, CNH6\",\"Pb2Br7, Lead bromide\",bis(butylaminium) methanaminium lead bromide,2,bulk polycrystalline,,,,,,,,\"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",Yellow plate-shaped crystals,\"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",,\r\n10.1021/jacs.8b12948,Bis(butylammonium) methylammonium lead bromide,[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7,\"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\"C4H12N, CNH6\",\"Pb2Br7, Lead bromide\",bis(butylaminium) methanaminium lead bromide,2,single crystal,,,,,,,,\"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",Yellow plate-shaped crystals,\"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",AC impedance measurement,\"Samples were prepared by cutting single crystals along the c-axis, coating crystals with silver conduction paste. The real έ was measured with two-probe AC impedance method (Impedance Analyzer TH2828A).\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) methylammonium lead iodide,(CH3(CH2)4NH3)2(MA)Pb2I7,\"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\"C5NH14, CNH6\",\"Pb2I7, Lead iodide\",bis(pentylaminium) methanaminium lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 μL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Single crystal X-Ray diffraction,A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ=0.71073 Å) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\r\n10.1021/jacs.9b01327,Bis(pentylammonium) methylammonium lead iodide,(CH3(CH2)4NH3)2(MA)Pb2I7,\"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\"C5NH14, CNH6\",\"Pb2I7, Lead iodide\",bis(pentylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 μL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) methylammonium lead iodide,(CH3(CH2)4NH3)2(MA)Pb2I7,\"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\"C5NH14, CNH6\",\"Pb2I7, Lead iodide\",bis(pentylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 μL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) methylammonium lead iodide,(CH3(CH2)4NH3)2(MA)Pb2I7,\"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\"C5NH14, CNH6\",\"Pb2I7, Lead iodide\",bis(pentylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 μL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) bis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)2Pb3I10,\"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C5NH14, CNH6\",\"Pb3I10, Lead iodide\",bis(pentylaminium) bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 μL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",Single crystal X-Ray diffraction,A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ=0.71073 Å) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\r\n10.1021/jacs.9b01327,Bis(pentylammonium) bis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)2Pb3I10,\"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C5NH14, CNH6\",\"Pb3I10, Lead iodide\",bis(pentylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 μL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) methylammonium lead iodide,(CH3(CH2)4NH3)2(MA)Pb2I7,\"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\"C5NH14, CNH6\",\"Pb2I7, Lead iodide\",bis(pentylaminium) methanaminium lead iodide,2,unknown,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 μL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",,\r\n10.1021/jacs.9b01327,Bis(pentylammonium) bis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)2Pb3I10,\"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C5NH14, CNH6\",\"Pb3I10, Lead iodide\",bis(pentylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 μL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) bis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)2Pb3I10,\"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C5NH14, CNH6\",\"Pb3I10, Lead iodide\",bis(pentylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 μL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tris(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)3Pb4I13,\"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C5NH14, CNH6\",\"Pb4I13, Lead iodide\",bis(pentylaminium) tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",Single crystal X-Ray diffraction,A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ=0.71073 Å) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\r\n10.1021/jacs.9b01327,Bis(pentylammonium) methylammonium lead iodide,(CH3(CH2)4NH3)2(MA)Pb2I7,\"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\"C5NH14, CNH6\",\"Pb2I7, Lead iodide\",bis(pentylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tris(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)3Pb4I13,\"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C5NH14, CNH6\",\"Pb4I13, Lead iodide\",bis(pentylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tris(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)3Pb4I13,\"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C5NH14, CNH6\",\"Pb4I13, Lead iodide\",bis(pentylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tris(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)3Pb4I13,\"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C5NH14, CNH6\",\"Pb4I13, Lead iodide\",bis(pentylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tris(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)3Pb4I13,\"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C5NH14, CNH6\",\"Pb4I13, Lead iodide\",bis(pentylaminium) tris(methanaminium) lead iodide,2,unknown,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 μL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) bis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)2Pb3I10,\"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C5NH14, CNH6\",\"Pb3I10, Lead iodide\",bis(pentylaminium) bis(methanaminium) lead iodide,2,unknown,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask. The solution was heated and stirred constantly. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine was added to 50% aqueous H3PO2 (2 mL) and solution reacted slowly. The solution was cooled on a hot plate and eventually cooled to room temperature. After three hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)4Pb5I16,\"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C5NH14, CNH6\",\"Pb5I16, Lead iodide\",bis(pentylaminium) tetrakis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",Single crystal X-Ray diffraction,A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ=0.71073 Å) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)4Pb5I16,\"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C5NH14, CNH6\",\"Pb5I16, Lead iodide\",bis(pentylaminium) tetrakis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)4Pb5I16,\"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C5NH14, CNH6\",\"Pb5I16, Lead iodide\",bis(pentylaminium) tetrakis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) bis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)2Pb3I10,\"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C5NH14, CNH6\",\"Pb3I10, Lead iodide\",bis(pentylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 μL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)4Pb5I16,\"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C5NH14, CNH6\",\"Pb5I16, Lead iodide\",bis(pentylaminium) tetrakis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tris(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)3Pb4I13,\"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C5NH14, CNH6\",\"Pb4I13, Lead iodide\",bis(pentylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) methylammonium lead iodide,(CH3(CH2)5NH3)2(MA)Pb2I7,\"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\"C6NH16, CNH6\",\"Pb2I7, Lead iodide\",bis(hexylaminium) methanaminium lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 μL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Single crystal X-Ray diffraction,A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ=0.71073 Å) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tris(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)3Pb4I13,\"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C5NH14, CNH6\",\"Pb4I13, Lead iodide\",bis(pentylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) methylammonium lead iodide,(CH3(CH2)5NH3)2(MA)Pb2I7,\"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\"C6NH16, CNH6\",\"Pb2I7, Lead iodide\",bis(hexylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 μL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) methylammonium lead iodide,(CH3(CH2)5NH3)2(MA)Pb2I7,\"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\"C6NH16, CNH6\",\"Pb2I7, Lead iodide\",bis(hexylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 μL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) methylammonium lead iodide,(CH3(CH2)5NH3)2(MA)Pb2I7,\"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\"C6NH16, CNH6\",\"Pb2I7, Lead iodide\",bis(hexylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 μL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) bis(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)2Pb3I10,\"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C6NH16, CNH6\",\"Pb3I10, Lead iodide\",bis(hexylaminium) bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 μL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Single crystal X-Ray diffraction,A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ=0.71073 Å) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\r\n10.1021/jacs.9b01327,Bis(hexylammonium) bis(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)2Pb3I10,\"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C6NH16, CNH6\",\"Pb3I10, Lead iodide\",bis(hexylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 μL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)4Pb5I16,\"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C5NH14, CNH6\",\"Pb5I16, Lead iodide\",bis(pentylaminium) tetrakis(methanaminium) lead iodide,2,unknown,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask. The solution was heated and stirred constantly. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine was added to 50% aqueous H3PO2 (2 mL) and solution reacted slowly. The solution was cooled on a hot plate and eventually cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) bis(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)2Pb3I10,\"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C6NH16, CNH6\",\"Pb3I10, Lead iodide\",bis(hexylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 μL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) bis(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)2Pb3I10,\"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C6NH16, CNH6\",\"Pb3I10, Lead iodide\",bis(hexylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 μL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) tris(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)3Pb4I13,\"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6NH16, CNH6\",\"Pb4I13, Lead iodide\",bis(hexylaminium) tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Single crystal X-Ray diffraction,A Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ=0.71073 Å) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\r\n10.1021/jacs.9b01327,Bis(pentylammonium) tetrakis(methylammonium) lead iodide,(CH3(CH2)4NH3)2(MA)4Pb5I16,\"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\"C5NH14, CNH6\",\"Pb5I16, Lead iodide\",bis(pentylaminium) tetrakis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask. The solution was heated and stirred constantly. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 μL (2 mmol) of pentylamine was added to 50% aqueous H3PO2 (2 mL) and solution reacted slowly. The solution was cooled on a hot plate and eventually cooled to room temperature. After three hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) methylammonium lead iodide,(CH3(CH2)5NH3)2(MA)Pb2I7,\"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\"C6NH16, CNH6\",\"Pb2I7, Lead iodide\",bis(hexylaminium) methanaminium lead iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 μL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) methylammonium lead iodide,(CH3(CH2)5NH3)2(MA)Pb2I7,\"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\"C6NH16, CNH6\",\"Pb2I7, Lead iodide\",bis(hexylaminium) methanaminium lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",red plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 μL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) bis(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)2Pb3I10,\"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C6NH16, CNH6\",\"Pb3I10, Lead iodide\",bis(hexylaminium) bis(methanaminium) lead iodide,2,unknown,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 μL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) bis(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)2Pb3I10,\"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\"C6NH16, CNH6\",\"Pb3I10, Lead iodide\",bis(hexylaminium) bis(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",brown plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 μL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) tris(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)3Pb4I13,\"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6NH16, CNH6\",\"Pb4I13, Lead iodide\",bis(hexylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) tris(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)3Pb4I13,\"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6NH16, CNH6\",\"Pb4I13, Lead iodide\",bis(hexylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) tris(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)3Pb4I13,\"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6NH16, CNH6\",\"Pb4I13, Lead iodide\",bis(hexylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) tris(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)3Pb4I13,\"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6NH16, CNH6\",\"Pb4I13, Lead iodide\",bis(hexylaminium) tris(methanaminium) lead iodide,2,unknown,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) tris(methylammonium) lead iodide,(CH3(CH2)5NH3)2(MA)3Pb4I13,\"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6NH16, CNH6\",\"Pb4I13, Lead iodide\",bis(hexylaminium) tris(methanaminium) lead iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (≥98%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",black plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 μL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) lead iodide,(CH3(CH2)4NH3)2PbI4,\"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",C5H14N,\"PbI4, Lead iodide\",bis(pentylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 μL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) lead iodide,(CH3(CH2)4NH3)2PbI4,\"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",C5H14N,\"PbI4, Lead iodide\",bis(pentylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 μL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) lead iodide,(CH3(CH2)4NH3)2PbI4,\"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",C5H14N,\"PbI4, Lead iodide\",bis(pentylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 μL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) lead iodide,(CH3(CH2)4NH3)2PbI4,\"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",C5H14N,\"PbI4, Lead iodide\",bis(pentylaminium) lead (II) iodide,2,unknown,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 μL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) lead iodide,(CH3(CH2)5NH3)2PbI4,\"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",C6H16N,\"PbI4, Lead iodide\",bis(hexylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 μL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(pentylammonium) lead iodide,(CH3(CH2)4NH3)2PbI4,\"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",C5H14N,\"PbI4, Lead iodide\",bis(pentylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 μL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) lead iodide,(CH3(CH2)5NH3)2PbI4,\"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",C6H16N,\"PbI4, Lead iodide\",bis(hexylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 μL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) lead iodide,(CH3(CH2)5NH3)2PbI4,\"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",C6H16N,\"PbI4, Lead iodide\",bis(hexylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 μL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) lead iodide,(CH3(CH2)5NH3)2PbI4,\"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",C6H16N,\"PbI4, Lead iodide\",bis(hexylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 μL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",Photoluminescence microscopy,\"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\"\r\n10.1021/jacs.9b01327,Bis(hexylammonium) lead iodide,(CH3(CH2)5NH3)2PbI4,\"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",C6H16N,\"PbI4, Lead iodide\",bis(hexylaminium) lead (II) iodide,2,bulk polycrystalline,,,,,,,,\"Lead(II) oxide (PbO, <10 μm, ReagentPlus®, ≥99.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",orange plate-like crystals,\"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 μL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",UV-vis absorption (diffused reflectance),\"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1-R)^{2}/2R.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) lead bromide,C20H44Br4N2Pb,\"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",C10H22N,\"PbBr4, Lead bromide\",bis(N-butyl-N-methyl-piperidinium) lead bromide,0,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",single crystals,\"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",Single-crystal X-ray diffraction,A Bruker Smart Platform diffractometer with Apex I CCD detector and MoKα radiation (λ = 0.71073 Å) and an Oxford Xcalibur S diffractometer with Sapphire 3 CCD detector and MoKα radiation (λ = 0.71073 Å) were used.\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) lead bromide,C20H44Br4N2Pb,\"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",C10H22N,\"PbBr4, Lead bromide\",bis(N-butyl-N-methyl-piperidinium) lead bromide,0,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",single crystals,\"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",Melting point measurement,A BUCHI M-565 Melting point instrument was used to collect data.\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) lead bromide,C20H44Br4N2Pb,\"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",C10H22N,\"PbBr4, Lead bromide\",bis(N-butyl-N-methyl-piperidinium) lead bromide,0,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",Photoluminescence,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) lead bromide,C20H44Br4N2Pb,\"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",C10H22N,\"PbBr4, Lead bromide\",bis(N-butyl-N-methyl-piperidinium) lead bromide,0,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",Photoluminescence,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) lead bromide,C20H44Br4N2Pb,\"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",C10H22N,\"PbBr4, Lead bromide\",bis(N-butyl-N-methyl-piperidinium) lead bromide,0,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",PLQY,\"A Quantaurus-QY spectrometer, developed from Hamamatsu, was used.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) lead bromide,C20H44Br4N2Pb,\"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",C10H22N,\"PbBr4, Lead bromide\",bis(N-butyl-N-methyl-piperidinium) lead bromide,0,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",Photoluminescence (PL) and PL excitation,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin bromide,C20H44Br4N2Sn,\"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",C10H22N,\"SnBr4, Tin bromide\",bis(N-butyl-N-methyl-piperidinium) tin bromide,0,single crystal,,,,,,,,\"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70ºC to room temperature, allowing crystals to grow.\",Single-crystal X-ray diffraction,A Bruker Smart Platform diffractometer with Apex I CCD detector and MoKα radiation (λ = 0.71073 Å) and an Oxford Xcalibur S diffractometer with Sapphire 3 CCD detector and MoKα radiation (λ = 0.71073 Å) were used.\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin bromide,C20H44Br4N2Sn,\"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",C10H22N,\"SnBr4, Tin bromide\",bis(N-butyl-N-methyl-piperidinium) tin bromide,0,single crystal,,,,,,,,\"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70ºC to room temperature, allowing crystals to grow.\",Melting point measurement,A BUCHI M-565 Melting point instrument was used to collect data.\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin bromide,C20H44Br4N2Sn,\"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",C10H22N,\"SnBr4, Tin bromide\",bis(N-butyl-N-methyl-piperidinium) tin bromide,0,unknown,,,,,,,,\"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70ºC to room temperature, allowing crystals to grow.\",Photoluminescence,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin bromide,C20H44Br4N2Sn,\"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",C10H22N,\"SnBr4, Tin bromide\",bis(N-butyl-N-methyl-piperidinium) tin bromide,0,single crystal,,,,,,,,\"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",single crystals,\"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70ºC to room temperature, allowing crystals to grow.\",Photoluminescence,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin bromide,C20H44Br4N2Sn,\"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",C10H22N,\"SnBr4, Tin bromide\",bis(N-butyl-N-methyl-piperidinium) tin bromide,0,single crystal,,,,,,,,\"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70ºC to room temperature, allowing crystals to grow.\",PLQY measurement,\"A Quantaurus-QY spectrometer, developed from Hamamatsu, was used.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin bromide,C20H44Br4N2Sn,\"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",C10H22N,\"SnBr4, Tin bromide\",bis(N-butyl-N-methyl-piperidinium) tin bromide,0,single crystal,,,,,,,,\"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",Single crystals,\"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70ºC to room temperature, allowing crystals to grow.\",Photoluminescence and Photoluminescence excitation,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) germanium bromide,C20H44Br4GeN2,\"Bmpip2GeBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromogermaniate(II)\",C10H22N,\"GeBr4, Germanium bromide\",bis(N-butyl-N-methyl-piperidinium) germanium bromide,0,single crystal,,,,,,,,\"germanium(II) bromide (GeBr2, 97%, Aldrich-Fine Chemicals, 5 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), ethanol, EtOH (anhydrous, 99.8%, Acros Organics, 1 L)\",single crystals,\"First, GeBr2 (0.5 mmol) and BmpipBr (1 mmol) were dissolved in 3 mL of EtOH. Then, 2 mL of Et2O was added to the EtOH solution, and single crystals began to grow at the interface.\",Single-crystal X-ray diffraction,A Bruker Smart Platform diffractometer with Apex I CCD detector and MoKα radiation (λ = 0.71073 Å) and an Oxford Xcalibur S diffractometer with Sapphire 3 CCD detector and MoKα radiation (λ = 0.71073 Å) were used.\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) germanium bromide,C20H44Br4GeN2,\"Bmpip2GeBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromogermaniate(II)\",C10H22N,\"GeBr4, Germanium bromide\",bis(N-butyl-N-methyl-piperidinium) germanium bromide,0,single crystal,,,,,,,,\"germanium(II) bromide (GeBr2, 97%, Aldrich-Fine Chemicals, 5 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), ethanol, EtOH (anhydrous, 99.8%, Acros Organics, 1 L)\",single crystals,\"First, GeBr2 (0.5 mmol) and BmpipBr (1 mmol) were dissolved in 3 mL of EtOH. Then, 2 mL of Et2O was added to the EtOH solution, and single crystals began to grow at the interface.\",Photoluminescence,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) germanium bromide,C20H44Br4GeN2,\"Bmpip2GeBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromogermaniate(II)\",C10H22N,\"GeBr4, Germanium bromide\",bis(N-butyl-N-methyl-piperidinium) germanium bromide,0,single crystal,,,,,,,,\"germanium(II) bromide (GeBr2, 97%, Aldrich-Fine Chemicals, 5 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), ethanol, EtOH (anhydrous, 99.8%, Acros Organics, 1 L)\",single crystals,\"First, GeBr2 (0.5 mmol) and BmpipBr (1 mmol) were dissolved in 3 mL of EtOH. Then, 2 mL of Et2O was added to the EtOH solution, and single crystals began to grow at the interface.\",Photoluminescence and PL excitation,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin iodide,C20H44I4N2Sn,\"Bmpip2SnI4, Bis(1-butyl-1-methyl-piperidinium) tetraiodostannate(II)\",C10H22N,\"SnI4, Tin iodide\",bis(N-butyl-N-methyl-piperidinium) tin iodide,0,single crystal,,,,,,,,\"tin(II) iodide (99%, Strem Chemicals, 25 g),1-butyl-1-methylpiperidinium iodide, BmpipI (>98%, IOLITEC, 50 g), acetone, γ-butyrolactone, GBL (99+%, Acros Organics, 1 L)\",single crystals,\"First, SnI2 (1 mmol) and BmpipI (2 mmol) were dissolved in GBL (4 mL). After acetone was added, beige powder resulted. Crystals were grown by cooling stock GBL to room temperature from 90ºC.\",Photoluminescence,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin iodide,C20H44I4N2Sn,\"Bmpip2SnI4, Bis(1-butyl-1-methyl-piperidinium) tetraiodostannate(II)\",C10H22N,\"SnI4, Tin iodide\",bis(N-butyl-N-methyl-piperidinium) tin iodide,0,single crystal,,,,,,,,\"tin(II) iodide (99%, Strem Chemicals, 25 g),1-butyl-1-methylpiperidinium iodide, BmpipI (>98%, IOLITEC, 50 g), acetone, γ-butyrolactone, GBL (99+%, Acros Organics, 1 L)\",single crystals,\"First, SnI2 (1 mmol) and BmpipI (2 mmol) were dissolved in GBL (4 mL). After acetone was added, beige powder resulted. Crystals were grown by cooling stock GBL to room temperature from 90ºC.\",Photoluminescence and PL excitation,\"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\"\r\n10.1021/jacs.9b02365,Bis(1-butyl-1-methyl-piperidinium) tin iodide,C20H44I4N2Sn,\"Bmpip2SnI4, Bis(1-butyl-1-methyl-piperidinium) tetraiodostannate(II)\",C10H22N,\"SnI4, Tin iodide\",bis(N-butyl-N-methyl-piperidinium) tin iodide,0,single crystal,,,,,,,,\"tin(II) iodide (99%, Strem Chemicals, 25 g),1-butyl-1-methylpiperidinium iodide, BmpipI (>98%, IOLITEC, 50 g), acetone, γ-butyrolactone, GBL (99+%, Acros Organics, 1 L)\",single crystals,\"First, SnI2 (1 mmol) and BmpipI (2 mmol) were dissolved in GBL (4 mL). After acetone was added, beige powder resulted. Crystals were grown by cooling stock GBL to room temperature from 90ºC.\",PLQY measurements,\"A Quantaurus-QY spectrometer, developed from Hamamatsu, was used.\"\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,single crystal,,,,,,,,\"[AE2T].2HI (synthesized), BiI3, AgI, hydriodic acid (58 wt. % in H2O)\",dark red [AE2T]2AgBiI8 single crystals,\"Stoichiometric quantities of [AE2T].2HI (7.8 μmoles), BiI3 (3.9 μmoles) and AgI (3.9 μmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 2 ml deionized water at 100° C for 30 min. The solution was then slowly cooled to room temperature over 60 hrs. The as-obtained dark red crystals (~ 82 % yield) were filtered, washed with copious amounts of diethyl ether, dried in vacuum and stored in a N2 glove box for further characterization.\",Single crystal X-ray diffraction,SC-XRD was performed with Mo-Kα radiation (λ=0.710 Å) using a Bruker APEX II CCD diffractometer operating at 50 kV and 30 mA.\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,single crystal,,,,,,,,\"[AE2T].2HI (synthesized), BiI3, AgI, hydriodic acid (58 wt. % in H2O)\",dark red [AE2T]2AgBiI8 single crystals,\"Stoichiometric quantities of [AE2T].2HI (7.8 μmoles), BiI3 (3.9 μmoles) and AgI (3.9 μmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 2 ml deionized water at 100° C for 30 min. The solution was then slowly cooled to room temperature over 60 hrs. The as-obtained dark red crystals (~ 82 % yield) were filtered, washed with copious amounts of diethyl ether, dried in vacuum and stored in a N2 glove box for further characterization.\",Single crystal X-ray diffraction,SC-XRD was performed with Mo-Kα radiation (λ=0.710 Å) using a Bruker APEX II CCD diffractometer operating at 50 kV and 30 mA.\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,film,,,,,,,,\"[AE2T].2HI, BiI3, Ag,  hydriodic acid (58 wt. % in H2O), anhydrous dimethylformamide\",[AE2T]2AgBiI thin film,\"Stoichiometric amounts of [AE2T].2HI (0.024 mmoles), BiI3 (0.012 mmoles) and AgI (0.012 mmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 4 ml deionized water at 100° C for 30 min. The solution was cooled to room temperature and the resulting dark red precipitate was collected by centrifugation, washed with diethyl ether, and dried in vacuum. The solid powder was dissolved in 80 μL of anhydrous dimethylformamide. 40 μL of the solution was spin-coated on pre-cleaned glass substrates at a spin speed of 1500 RPM for 30 s, and annealed at 150° C on a hot plate for 10 min in a N2-filled glove box.\",UV-vis absorption,Shimadzu UV-3600 UV−vis-NIR spectrophotometer\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,film,,,,,,,,\"[AE2T].2HI, BiI3, Ag, hydriodic acid (58 wt. % in H2O), anhydrous dimethylformamide\",[AE2T]2AgBiI thin film,\"Stoichiometric amounts of [AE2T].2HI (0.024 mmoles), BiI3 (0.012 mmoles) and AgI (0.012 mmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 4 ml deionized water at 100° C for 30 min. The solution was cooled to room temperature and the resulting dark red precipitate was collected by centrifugation, washed with diethyl ether, and dried in vacuum. The solid powder was dissolved in 80 μL of anhydrous dimethylformamide. 40 μL of the solution was spin-coated on pre-cleaned glass substrates at a spin speed of 1500 RPM for 30 s, and annealed at 150° C on a hot plate for 10 min in a N2-filled glove box.\",UV-vis absorption,Shimadzu UV-3600 UV−vis-NIR spectrophotometer\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,film,,,,,,,,\"[AE2T].2HI, BiI3, Ag, hydriodic acid (58 wt. % in H2O), anhydrous dimethylformamide\",[AE2T]2AgBiI thin film,\"Stoichiometric amounts of [AE2T].2HI (0.024 mmoles), BiI3 (0.012 mmoles) and AgI (0.012 mmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 4 ml deionized water at 100° C for 30 min. The solution was cooled to room temperature and the resulting dark red precipitate was collected by centrifugation, washed with diethyl ether, and dried in vacuum. The solid powder was dissolved in 80 μL of anhydrous dimethylformamide. 40 μL of the solution was spin-coated on pre-cleaned glass substrates at a spin speed of 1500 RPM for 30 s, and annealed at 150° C on a hot plate for 10 min in a N2-filled glove box.\",,\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,single crystal,FHI-aims,DFT,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,2nd variational non-self-consistent SOC,NAO,0.025 eV,,,,,\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,single crystal,FHI-aims,DFT,PBE+TS,2x5x5,atomic ZORA,NAO,0.005 eV/Angstrom,,,,,\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,single crystal,FHI-aims,DFT,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,2nd variational non-self-consistent SOC,NAO,0.05 eV,,,,,\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,single crystal,FHI-aims,DFT,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,2nd variational non-self-consistent SOC,NAO,0.05 eV,,,,,\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",2,single crystal,FHI-aims,DFT,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,2nd variational non-self-consistent SOC,NAO,0.05,,,,,\r\n10.1021/jacs.9b02909,Cesium silver bismuth chloride,Cs2AgBiCl6,Dicesium trichloroargentate(I) µ-dichloro trichlorobismuthate(III),None,\"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",,3,single crystal,FHI-aims,DFT,PBE,30x30x30,2nd variational non-self-consistent SOC,NAO,0.05 eV,,,,,\r\n10.1021/jacs.9b02909,Cesium silver bismuth chloride,Cs2AgBiCl6,Dicesium trichloroargentate(I) µ-dichloro trichlorobismuthate(III),None,\"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",,3,single crystal,FHI-aims,DFT,PBE,30x30x30,2nd variational non-self-consistent SOC,NAO,0.05 eV,,,,,\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,FHI-aims tight,,,,,,\r\n10.1021/jacs.9b02909,\"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",C12H16N2S2AgBiI8,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) µ-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",C12H16N2S2,\"AgBiI8, Silver bismuth iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,FHI-aims tight,,,,,,\r\n10.1021/jacs.9b02909,Cesium silver bismuth chloride,Cs2AgBiCl6,Dicesium trichloroargentate(I) µ-dichloro trichlorobismuthate(III),None,\"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",,2,single crystal,FHI-aims,DFT,PBE,8*8*8,atomic ZORA with SOC,,,,,,,\r\n10.1021/jacs.9b02909,Cesium silver bismuth chloride,Cs2AgBiCl6,Dicesium trichloroargentate(I) µ-dichloro trichlorobismuthate(III),None,\"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",,3,single crystal,Wien2K,DFT,PBE,1000,Koelling-Harmon approximation + SOC,,,,,,,\r\n10.1021/jacs.9b02909,Bis(aminoethyl)-bithiophene lead iodide,C12H18N2S2PbI4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",C12H18N2S2,\"PbI4, Lead iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,atomic ZORA with spin-orbit-coupling,tight,,,,,,\r\n10.1021/jacs.9b05124,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"PbCO3 (2.67 g, 0.01 mol), CH3(CH2)3NH3I (1.34 g, 0.0067 mol), CH3CH2NH3I (1.15 g, 0.0067 mol)\",\"FEP, AFEP, PEP\",\"Lead iodide hybrid perovskites, (BA)2,(EA)2Pb3I10, were synthesized in a concentrated HI solution (40 mL, 57%) that contained PbCO3, CH3(CH2)3NH3I, CH3CH2NH3I.\",\"Temperature-cooling, Powder X-RAY Diffraction and Differential Scanning Calorimetry (DSC)\",\"Crystals of the hydroiodic solutions were obtained via a temperature- cooling method using differential scanning calorimetry (DSC) measurements with a heating/cooling rate of 10 K/min. The DSC traced reversible thermal peaks at 322/315 K (T1) and 363/360 K (T2) in the heating/cooling mode. The preparation of the HI solutions performed at  50°C and kept at 4-6 °C above its preliminary saturated temperature. The temperature was then slowly lowered with a cooling rate of 0.5 K/day, which resulted in bulk dark-red crystals. In addition, a bright yellow solution was obtained from heating the synthesis of compound 1 in an HI solution.  These crystals were then verified via powder X-ray diffraction at room temperature. The temperature dependence of the dielectric constant was measured using the double-wave method to\"\r\n10.1021/jacs.9b06276,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,VASP 5.4.4,DFT,,4x2x2,,PAW,,,,,,\r\n10.1021/jacs.9b06276,\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",C40H40NS4SnI4,\"(4Tm)2SnI4, I16Sn4‚Ä¢8(C20H20NS4), Bis(2-(3‚Äù, 4‚Äô-dimethyl-[2,2‚Äô:5‚Äô,2‚Äô:5‚Äù,2‚Äù‚Äô-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",C20H20NS4,\"SnI4, Tin iodide\",\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",2,single crystal,,,,,,,,\"tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate, Pd2(dba)3, P(o-tol)¬3, tributyl(3,3”-dimethyl-[2,2’:5’,2”-terthiophen]-5-yl)stannane\",\"thin, dark red/black plate-like crystals\",\"The organic salt 4Tm-Boc was synthesized first by mixing tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate (612 mg, 2 mmol), Pd2(dba)3 (37 mg, 2 mol%), P(o-tol)¬3 (49 mg, 8 mol%) and tributyl(3,3”-dimethyl-[2,2’:5’,2”-terthiophen]-5-yl)stannane (2.2 mmol) in a 100 mL Schlenk tube. The air was then replaced with argon, and toluene (20 mL) was added to the mixture. The mixture was stirred for 0.5 hours at 100º C, cooled to room temperature, water was added, and the solution was extracted via dichloromethane (DCM). The organic layers were combined, washed, and dried. \r\n\r\nNext, 4Tm-Boc (1 mmol) was dissolved in 20 mL methanol, aqueous HI solution was added, and the solution was stirred for 6 hours. Solid 4TmI salt resulted.\r\n\r\nSingle crystals of (4Tm)2SnI4 were obtained by dissolving stoichiometric amounts of 4TmI and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene. This yielded thin dark red/black plates.\",Single-crystal X-Ray Diffraction,\"A Bruker Quest diffractometer with kappa geometry, I-μ-S microsource X-ray tube (Cu Kα radiation, λ = 1.54178 Å), Photon2 CMOS area detector, and multilayer mirror for monochromatization was used. Data was scanned and corrected with APEX3, space groups were solved using XPREP in SHELXTL\"\r\n10.1021/jacs.9b06276,\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",C40H40NS4SnI4,\"(4Tm)2SnI4, I16Sn4‚Ä¢8(C20H20NS4), Bis(2-(3‚Äù, 4‚Äô-dimethyl-[2,2‚Äô:5‚Äô,2‚Äô:5‚Äù,2‚Äù‚Äô-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",C20H20NS4,\"SnI4, Tin iodide\",\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",2,single crystal,VASP version 5.4.4,DFT,,4x4x2,,PAW,,,,,,\r\n10.1021/jacs.9b06276,\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",C40H40NS4SnI4,\"(4Tm)2SnI4, I16Sn4‚Ä¢8(C20H20NS4), Bis(2-(3‚Äù, 4‚Äô-dimethyl-[2,2‚Äô:5‚Äô,2‚Äô:5‚Äù,2‚Äù‚Äô-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",C20H20NS4,\"SnI4, Tin iodide\",\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",2,film,,,,,,,,\"tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate, Pd2(dba)3, P(o-tol)¬3, tributyl(3,3”-dimethyl-[2,2’:5’,2”-terthiophen]-5-yl)stannane\",film,\"The organic salt 4Tm-Boc was synthesized first by mixing tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate (612 mg, 2 mmol), Pd2(dba)3 (37 mg, 2 mol%), P(o-tol)¬3 (49 mg, 8 mol%) and tributyl(3,3”-dimethyl-[2,2’:5’,2”-terthiophen]-5-yl)stannane (2.2 mmol) in a 100 mL Schlenk tube. The air was then replaced with argon, and toluene (20 mL) was added to the mixture. The mixture was stirred for 0.5 hours at 100º C, cooled to room temperature, water was added, and the solution was extracted via dichloromethane (DCM). The organic layers were combined, washed, and dried. Next, 4Tm-Boc (1 mmol) was dissolved in 20 mL methanol, aqueous HI solution was added, and the solution was stirred for 6 hours. Solid 4TmI salt resulted. Single crystals of (4Tm)2SnI4 were obtained by dissolving stoichiometric amounts of 4TmI and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene. This yielded thin dark red/black plates.\r\n\r\n4TmI (53.0 mg, 100 μmol) and SnI2 (23.0 mg, 50 μmol) were dissolved in 1 mL of anhydrous DMF/DMSO (10/1) at 70 degrees C. The (4Tm)2SnI4 solution was allowed to cool to room temperature and was spin coated at 4000 rpm for 60 s on clean Si/SiO2 wafers or quartz slides. The films were annealed at 180 degrees C on a hot plate for 10 min in nitrogen.\",Photoluminescence,\r\n10.1021/jacs.9b06276,\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",C40H40NS4SnI4,\"(4Tm)2SnI4, I16Sn4‚Ä¢8(C20H20NS4), Bis(2-(3‚Äù, 4‚Äô-dimethyl-[2,2‚Äô:5‚Äô,2‚Äô:5‚Äù,2‚Äù‚Äô-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",C20H20NS4,\"SnI4, Tin iodide\",\"Bis(2-(3”, 4’-dimethyl-[2,2’:5’,2’:5”,2”’-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",2,film,,,,,,,,\"tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate, Pd2(dba)3, P(o-tol)¬3, tributyl(3,3”-dimethyl-[2,2’:5’,2”-terthiophen]-5-yl)stannane\",film,\"The organic salt 4Tm-Boc was synthesized first by mixing tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate (612 mg, 2 mmol), Pd2(dba)3 (37 mg, 2 mol%), P(o-tol)¬3 (49 mg, 8 mol%) and tributyl(3,3”-dimethyl-[2,2’:5’,2”-terthiophen]-5-yl)stannane (2.2 mmol) in a 100 mL Schlenk tube. The air was then replaced with argon, and toluene (20 mL) was added to the mixture. The mixture was stirred for 0.5 hours at 100º C, cooled to room temperature, water was added, and the solution was extracted via dichloromethane (DCM). The organic layers were combined, washed, and dried. Next, 4Tm-Boc (1 mmol) was dissolved in 20 mL methanol, aqueous HI solution was added, and the solution was stirred for 6 hours. Solid 4TmI salt resulted. Single crystals of (4Tm)2SnI4 were obtained by dissolving stoichiometric amounts of 4TmI and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene. This yielded thin dark red/black plates. 4TmI (53.0 mg, 100 μmol) and SnI2 (23.0 mg, 50 μmol) were dissolved in 1 mL of anhydrous DMF/DMSO (10/1) at 70 degrees C. The (4Tm)2SnI4 solution was allowed to cool to room temperature and was spin coated at 4000 rpm for 60 s on clean Si/SiO2 wafers or quartz slides. The films were annealed at 180 degrees C on a hot plate for 10 min in nitrogen.\",UV-vis absorption,Obtained using an Agilent UV-Vis-NIR Cary-5000 spectrometer in transmission mode.\r\n10.1021/jacs.9b06276,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"phenylethylammonium iodide (PEAI), tin (II) iodide (SnI2), gamma-bytrolactone (GBL)\",Red plate-like crystals,\"Single crystals of were obtained by dissolving stoichiometric amounts of the organic salt and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene.\",Single-crystal X-Ray Diffraction,\"A Bruker Quest diffractometer with kappa geometry, I-μ-S microsource X-ray tube (Cu Kα radiation, λ = 1.54178 Å), Photon2 CMOS area detector, and multilayer mirror for monochromatization was used. Data was scanned and corrected with APEX3, space groups were solved using XPREP in SHELXTL\"\r\n10.1021/jacs.9b06398,3-(aminomethyl)pyridinium lead iodide,C6H10N2PbI4,\"(3AMPY)PbI4, (C6H10N2)PbI4, 3-(methanaminium)pyridinium tetraiodoplumbate(II)\",C6H10N2,\"PbI4, lead iodide\",3-(methanaminium)pyridinium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, 3-(aminomethyl)pyridine (3AMPY), Aq. HI, Aq. H3PO2\",Red plate-like (3AMPY)PbI4 crystal,\"To a hot yellow solution of 0.5 mmol PbO in 2.5 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.5 mmol 3AMPY neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-like crystals precipitate upon cooling the above to 120°C and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,3-(aminomethyl)pyridinium methylammonium lead iodide,C7H16N3Pb2I7,\"(3AMPY)(MA)Pb2I7, (C7H16N3)Pb2I7, 3-(methanaminium)pyridinium methanaminium septaiodo diplumbate(II)\",\"C6H10N2, CH6N\",\"Pb2I7, Lead iodide\",3-(methanaminium)pyridinium methanaminium lead iodide,2,single crystal,,,,,,,,\"PbO, CH3NH3Cl, Aq. HI, Aq. H3PO2, 3-(aminomethyl)pyridine\",Dark-red plate-like (3AMPY)(MA)Pb2I7 crystals,\"To a hot yellow solution of 2 mmol PbO and 1 mmol CH3NH3Cl in 2.75 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.7 mmol 3-(aminomethyl)pyridine (3AMPY) neutralized in 0.5 ml concentrated. Aq. H3PO2 was added under stirring. Dark red plate-shaped crystals precipitate upon cooling the above to 120°C, and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,3-(aminomethyl)pyridinium bis(methylammonium) lead iodide,C8H22N4Pb3I10,\"(3AMPY)(MA)2Pb3I10, (C8H22N4)Pb3I10, 3-(methanaminium)pyridinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H10N2, CH6N\",\"Pb3I10, Lead iodide\",3-(methanaminium)pyridinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, CH3NH3Cl, 3-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",Black plate-like (3AMPY)(MA)2Pb3I10 crystals,\"To a hot yellow solution of 1.5 mmol PbO and 1 mmol CH3NH3Cl in 2.25 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.2 mmol 3-(aminomethyl)pyridine (3AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Black plate-shaped crystals precipitate upon cooling the above to 120°C, and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,3-(aminomethyl)pyridinium tris(methylammonium) lead iodide,C9H28N5Pb4I13,\"(3AMPY)(MA)3Pb4I13, (C9H28N5)Pb4I13, 3-(methanaminium)pyridinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H10N2, CH6N\",\"Pb4I13, Lead iodide\",3-(methanaminium)pyridinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, CH3NH3Cl, 3-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",Black plate-like (3AMPY)(MA)3Pb4I13 crystals,\"To a hot yellow solution of 2 mmol PbO and 1.5 mmol CH3NH3Cl in 3.25 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.15 mmol 3-(aminomethyl)pyridine (3AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Black plate-shaped crystals precipitate upon cooling the above to 120°C, and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,4-(aminomethyl)pyridinium lead iodide,C6H10N2PbI4,\"(4AMPY)PbI4, (C6H10N2)PbI4, 4-(methanaminium)pyridinium tetraiodoplumbate(II)\",C6H10N2,\"PbI4, Lead iodide\",4-(methanaminium)pyridinium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",Red plate-like (4AMPY)PbI4 crystals,\"To a hot yellow solution of 0.5 mmol PbO in 2 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.5 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.4 ml concentrated Aq. H3PO2 was added under stirring. Orange plate-shaped crystals precipitate upon cooling the above to 120°C.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,4-(aminomethyl)pyridinium methylammonium lead iodide,C7H16N3Pb2I7,\"(4AMPY)(MA)Pb2I7, (C7H16N3)Pb2I7, 4-(methanaminium)pyridinium methanaminium septaiodo diplumbate(II)\",\"C6H10N2, CH6N\",\"Pb2I7, Lead iodide\",4-(methanaminium)pyridinium methanaminium lead iodide,2,single crystal,,,,,,,,\"PbO, CH3NH3Cl, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",Dark red plate-like (4AMPY)(MA)Pb2I7 crystals,\"To a hot yellow solution of 2 mmol PbO and 1 mmol CH3NH3Cl in 2.75 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.6 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-shaped crystals precipitate upon cooling the above to 120°C, and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,4-(aminomethyl)pyridinium bis(methylammonium) lead iodide,C8H22N4Pb3I10,\"(4AMPY)(MA)2Pb3I10, (C8H22N4)Pb3I10, 4-(methanaminium)pyridinium bis(methanaminium) decaiodo triplumbate(II)\",\"C6H10N2, CH6N\",\"Pb3I10, Lead iodide\",4-(methanaminium)pyridinium bis(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, CH3NH3Cl, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",Black plate-like (4AMPY)(MA)2Pb3I10 crystals,\"To a hot yellow solution of 1.5 mmol PbO and 1 mmol CH3NH3Cl in 2.5 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.25 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Dark red plate-shaped crystals precipitate upon cooling the above to 120°C, and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,4-(aminomethyl)pyridinium tris(methylammonium) lead iodide,C9H28N5Pb4I13,\"(4AMPY)(MA)3Pb4I13, (C9H28N5)Pb4I13, 4-(methanaminium)pyridinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\"C6H10N2, CH6N\",\"Pb4I13, Lead iodide\",4-(methanaminium)pyridinium tris(methanaminium) lead iodide,2,single crystal,,,,,,,,\"PbO, CH3NH3Cl, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",Black (4AMPY)(MA)3Pb4I13 crystals,\"To a hot yellow solution of 2 mmol PbO and 1.5 mmol CH3NH3Cl in 3.25 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.14 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Black plate-shaped crystals precipitate upon cooling the above to 120°C, and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,3-(aminomethyl)pyridinium lead iodide,C6H10N2PbI4,\"(3AMPY)PbI4, (C6H10N2)PbI4, 3-(methanaminium)pyridinium tetraiodoplumbate(II)\",C6H10N2,\"PbI4, lead iodide\",3-(methanaminium)pyridinium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, 3-(aminomethyl)pyridine (3AMPY), Aq. HI, Aq. H3PO2\",Red plate-like (3AMPY)PbI4 crystal,\"To a hot yellow solution of 0.5 mmol PbO in 2.5 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.5 mmol 3AMPY neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-like crystals precipitate upon cooling the above to 120°C and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b06398,3-(aminomethyl)pyridinium lead iodide,C6H10N2PbI4,\"(3AMPY)PbI4, (C6H10N2)PbI4, 3-(methanaminium)pyridinium tetraiodoplumbate(II)\",C6H10N2,\"PbI4, lead iodide\",3-(methanaminium)pyridinium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, 3-(aminomethyl)pyridine (3AMPY), Aq. HI, Aq. H3PO2\",Red plate-like (3AMPY)PbI4 crystal,\"To a hot yellow solution of 0.5 mmol PbO in 2.5 ml Aq. HI at 240°C (hot-plate temperature), a solution of 0.5 mmol 3AMPY neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-like crystals precipitate upon cooling the above to 120°C and further down to 80°C within 1 hr.\",Single-crystal X-ray diffraction,The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo Kα radiation (λ = 0.71073 Å) and operating at 50 kV and 40 mA.\r\n10.1021/jacs.9b07776,4-(aminomethyl)piperidinium lead iodide,C12H32I8N4Pb2,\"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",orange single-crystals,\"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110º C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",Single Crystal X-ray diffraction,\"A Bruker AXS D8 Venture Single Crystal X-ray Diffractometer with a Photon 100 CMOS active pixel sensor detector as well as a four-circle goniometer with Kappa geometry was used for SC-XRD. Software package APEX3 was used for data collection, reduction, and absorption correction. Structures were determined with the SHELXTL package.\"\r\n10.1021/jacs.9b07776,4-(aminomethyl)piperidinium lead iodide,C12H32I8N4Pb2,\"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",orange single-crystals,\"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110º C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",Single Crystal X-ray diffraction,\"A Bruker AXS D8 Venture Single Crystal X-ray Diffractometer with a Photon 100 CMOS active pixel sensor detector as well as a four-circle goniometer with Kappa geometry was used for SC-XRD. Software package APEX3 was used for data collection, reduction, and absorption correction. Structures were determined with the SHELXTL package.\"\r\n10.1021/jacs.9b07776,4-(aminomethyl)piperidinium lead iodide,C12H32I8N4Pb2,\"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",orange single-crystals,\"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110º C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",Photoluminescence,The spectrum was recorded using a Horiba Fluorolog.\r\n10.1021/jacs.9b07776,4-(aminomethyl)piperidinium lead iodide,C12H32I8N4Pb2,\"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,powder,,,,,,,,\"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",orange single-crystals,\"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110º C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",UV-vis absorbance,Solid state diffuse reflectance UV-vis spectra were measured via a UV-2450-Shimadzu UV-visible spectrometer.\r\n10.1021/jacs.9b07776,4-(aminomethyl)piperidinium lead iodide,C12H32I8N4Pb2,\"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",orange single-crystals,\"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110º C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",Photoluminescence,The spectrum was recorded using a Horiba Fluorolog.\r\n10.1021/jacs.9b07776,4-(aminomethyl)piperidinium lead iodide,C12H32I8N4Pb2,\"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,single crystal,,,,,,,,\"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",orange single-crystals,\"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110º C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",Photoluminescence,The spectrum was recorded using a Horiba Fluorolog.\r\n10.1021/jacs.9b07776,4-(aminomethyl)piperidinium lead iodide,C12H32I8N4Pb2,\"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",C6H16N2,\"PbI4, Lead iodide\",4-(methanaminium)piperidinium lead (II) iodide,2,powder,,,,,,,,\"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",orange single-crystals,\"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110º C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",UV-vis absorbance,Solid state diffuse reflectance UV-vis spectra were measured via a UV-2450-Shimadzu UV-visible spectrometer.\r\n10.1021/jp503337a,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,,,\"Refer to experimental from J. Lumin. 1994, 60&61, 269−274.\",Absorption spectra,\"Experimental data taken from J. Lumin. 1994, 60&61, 269−274 recorded at 159 K (black line) and 212 K (blue line) and computed spectra for bound and continuum pair states, considering two-particle wave function and effective mass equations for electron and hole (expression 3 with γ = 0.03 eV and μ = 0.16me). Structural phase transition occurs at Tc = 162 K (black dashed line). Refer to Fig. 3 and plots from J. Lumin. 1994, 60&61, 269−274.\"\r\n10.1038/ncomms11330,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"PbI2, Si substrate, etc.\",MAPbI3 Thin-film on Si,\"Prepare PbI2 aqueous solution (0.1 g per 100 ml) at 80 °C and cool to room temperature, which leads to the formation of suspended PbI2 microplates. For the PL measurement samples, dip the Si substrates with 300nm SiO2 (with pre-fabricated markers by photolithography) into the aqueous solution for a few seconds. For the FET samples, define the 5 nm Cr/50nm Au (Pt) electrodes with channel lengths of 8 and 40 mm by photolithography followed by thermal evaporation and lift-off. Grow PbI2 microplates onto the pre-fabricated electrodes by randomly dispersion. Convert the prepared PbI2 microplates into CH3NH3PbI3 by vapour phase intercalation. Refer to source for more details.\",Temperature-dependent transport measurement,\"The thickness of the perovskite microplates was determined by tapping-mode atomic force microscopy (Vecco 5,000 system). TEM images and SAED patterns were acquired in an FEI Titan high-resolution transmission microscopy. \r\n\r\nTemperature-dependent FET device measurements were carried out in a probe station ((Lakeshore, TTP4) coupled with a precision source/measurement unit (Agilent B2902A). The scanning rate for the transport measurement is 20V/s and the devices were pre-biased at the opposite voltage for 30 s before each measurement.\r\n\r\nRefer to Page 3; Page 4 figure 2.\"\r\n10.1038/ncomms11330,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"PbI2, Si substrate, etc.\",MAPbI3 Thin-film on Si,\"Prepare PbI2 aqueous solution (0.1 g per 100 ml) at 80 °C and cool to room temperature, which leads to the formation of suspended PbI2 microplates. For the PL measurement samples, dip the Si substrates with 300nm SiO2 (with pre-fabricated markers by photolithography) into the aqueous solution for a few seconds. For the FET samples, define the 5 nm Cr/50nm Au (Pt) electrodes with channel lengths of 8 and 40 mm by photolithography followed by thermal evaporation and lift-off. Grow PbI2 microplates onto the pre-fabricated electrodes by randomly dispersion. Convert the prepared PbI2 microplates into CH3NH3PbI3 by vapour phase intercalation. Refer to source for more details.\",Temperature-dependent photoluminescence,\"The thickness of the perovskite microplates was determined by tapping-mode atomic force microscopy (Vecco 5,000 system). TEM images and SAED patterns were acquired in an FEI Titan high-resolution transmission microscopy. \r\n\r\nThe PL measurement was conducted under a confocal micro-Raman system (Horiba LABHR) equipped with a 600 g/mm grating in a backscattering configuration excited by an Ar ion laser (488 nm). For the low-temperature measurement, a liquid nitrogen continuous flow cryostat (Cryo Industry of America) was used to control the temperature from 77 to 300 K.\r\n\r\nKeeping track of the P2/P1 intensity ratio. Increased P2/P1 intensity ratio with decreasing temperature (Fig. 5a and Supplementary Fig. 8).\"\r\n10.1038/ncomms14051,\"N, N′-dimethylethylenediamine lead bromide\",C4H14N2PbBr4,\"N, N‚Ä≤-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N, N′-dimethylethylenediaminium lead (II) bromide\",1,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 99.999%), N, N'-dimethylethylenediamine (99%), hydrobromic acid (HBr, 48 wt.% in H2O)\",Colorless needle-like C4N2H14PbBr4 crystals,\"In 10 ml HBr, PbBr2 (0.100 g, 0.27 mmol) and N, N' -dimethylethylenediamine (0.024 g, 0.27 mmol) were dissolved by sonication for 10 minutes. 1 mL of this solution was kept in a vapor diffusion chamber. Acetone was diffused into this solution for 24 h.\",single-crystal X-ray diffraction,The data were collected on a Bruker SMART APEX II diffractometer using Mo Kα radiation (λ = 0.71073 Å).\r\n10.1038/ncomms14051,\"N, N′-dimethylethylenediamine lead bromide\",C4H14N2PbBr4,\"N, N‚Ä≤-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"N, N′-dimethylethylenediaminium lead (II) bromide\",1,single crystal,,,,,,,,\"Lead (II) bromide (PbBr2, 99.999%), N, N'-dimethylethylenediamine (99%), hydrobromic acid (HBr, 48 wt.% in H2O)\",Colorless needle-like C4N2H14PbBr4 crystals,\"In 10 ml HBr, PbBr2 (0.100 g, 0.27 mmol) and N, N' -dimethylethylenediamine (0.024 g, 0.27 mmol) were dissolved by sonication for 10 minutes. 1 mL of this solution was kept in a vapor diffusion chamber. Acetone was diffused into this solution for 24 h.\",single-crystal X-ray diffraction,The data were collected on a Bruker SMART APEX II diffractometer using Mo Kα radiation (λ = 0.71073 Å).\r\n10.1038/ncomms4586,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"MAI, PbI2, DMF, Si glass\",MAPbI3 Thin-film on Si,\"Dissolve methylammonium iodide and lead (II) iodide (Sigma-Aldrich) in anhydrous N,N-Dimethylformamide (DMF) at a 3:1 molar ratio of MAI to PbI2, with final concentrations of 2.64M methylammonium iodide. The perovskite layer was then formed by spin coating the precursor solutions directly on the glass substrate at 2,000 r.p.m. in air. The flat and thin meso samples were spin coated without dilution but mesoporous samples were spin coated from diluted (three parts in four) precursor solutions. After spin coating, anneal the CH3NH3PbI3 at 150°C for 15 min.\",UV-Vis absorption,\"Absorption measurements were performed using a spectrophotometer (Perkin Elmer Lambda 1050) and a continuous flow static exchange gas cryostat (Oxford Instruments Optistat CF). The cryostat consist of three chambers, one inside the other. The sample is housed inside the internal chamber filled with gaseous He. The cryogenic liquid (He) is fluxed inside the second chamber allowing temperature control of the He atmosphere of the sample chamber. Eventually, a third chamber is evacuated (~10^-5–10^-6 mbar) in order to assure thermal isolation from the external ambient. Refer to Fig. 1.\"\r\n10.1038/s41427-019-0131-0,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,single crystal,,,,,,,,\"MACl (TCI, >98.0%), PbCl2 (Aldrich, 98.0%), dimethyl sulfoxide (DMSO) (Wako), and N, N-dimethylformamide (DMF) (Wako)\",Single crystalline colorless MAPbCl3 with the size of several hundred micrometers,\"Optical trapping induced crystallization:\r\n1:1 MACl/PbCl2 (1.0 M) were dissolved in DMSO: DMF solvent mixture (1:1, v-v) to prepare the precursor solution. The solution was centrifuged at 10,000 r.p.m for 5 min; the supernatant was used for further experiments. \r\n10 μL of the supernatant solution was used to prepare a thin layer (100-200 um thickness) in a laboratory-built sample chamber. A near-infrared (NIR) laser (Spectron Laser System, λ = 1064 nm) was focused onto the solution surface through an objective lens at 60 times magnification (Olympus UPlanFLN with a numerical aperture of 0.90).\",Single crystal X-ray diffraction,The crystal was mounted on the glass capillary and fixed with epoxy resin. Crystallographic data were collected using a Rigaku RAXIS-RAPID diffractometer with Mo-Kα (λ = 0.71073 Å) radiation from a graphite monochromator. Structural refinements were performed using the full-matrix least-squares method on F2. The calculations were carried out with the Yadokari-XG software.\r\n10.1038/s41467-019-08980-x,3-fluorophenethylammonium lead iodide,C16H22N2F2PbI4,\"3-fluorophenethanaminium tetraiodoplumbate(II), mF1PEA2PbI4\",C8H11NF,\"PbI4, Lead iodide\",3-fluorophenethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbI2 (99.9985%, from Alfa Aesar), HI, 3-fluorophenethylammonium iodide (synthesized)\",Orange crystals,26.4 mg PbI2 and 30.7 mg 3-fluorophenethylammonium iodide were dissolved in 1 ml 57 wt% stabilized HI at 90°C. The solution was slowly cooled down to room temperature at a rate of 1°C/h and the solids were collected.,Single crystal X-ray diffraction,Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo Kα radiation (λ=0.71073 Å) source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\r\n10.1038/s41467-019-08980-x,2-fluorophenethylammonium lead iodide,C16H22N2F2PbI4,\"2-fluorophenethanaminium tetraiodoplumbate(II), oF1PEA2PbI4\",C8H11NF,\"PbI4, Lead iodide\",2-fluorophenethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbI2 (99.9985%, from Alfa Aesar), HI, 2-fluorophenethylammonium iodide (synthesized)\",Orange-yellow crystals,26.4 mg PbI2 and 30.7 mg 2-fluorophenethylammonium iodide were dissolved in 1 ml 57 wt% stabilized HI at 90°C. The solution was slowly cooled down to room temperature at a rate of 1°C/h and the solids were collected.,Single crystal X-ray diffraction,Bruker D8 Quest ECO diffractometer equipped with a microfocus  Mo Kα radiation (λ=0.71073 Å) source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\r\n10.1038/s41467-019-08980-x,4-fluorophenethylammonium lead iodide,C16H22N2F2PbI4,\"4-fluorophenethanaminium tetraiodoplumbate(II), pF1PEA2PbI4\",C8H11NF,\"PbI4, Lead iodide\",4-fluorophenethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbI2 (99.9985%, from Alfa Aesar), 4-fluorophenethylammonium iodide (synthesized), HI\",Orange rectangular crystal,26.4 mg PbI2 and 30.7 mg 4-fluorophenethylammonium iodide were dissolved in 1.5 ml 57 wt% stabilized HI at 90°C. The solution was slowly cooled down to room temperature at a rate of 1°C/h and the solids were collected.,Single crystal X-ray diffraction,Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo Kα radiation (λ=0.71073 Å) source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\r\n10.1038/s41467-020-18485-7,S-1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"S-NEA2PbBr4, S-1-(1-naphthyl)ethanaminium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",S-1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,,,,,,,,\"S-1-(1-naphthyl)ethylamine, PbBr2\",S-1-(1-naphthyl)ethylammonium lead bromide,\"A hot solution of PbBr2 (45 mg, 0.12 mmol) and S-1-(1-naphthyl)ethylamine (39 µL, 0.24 mmol ) in 0.5 ml aq. HBr and 1.2 ml deionized water in a sealed vial with an N2 atmosphere was slowly cooled from 95 °C to room temperature over 48 hr. The colorless, plate-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-020-18485-7,R-1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"R-NEA2PbBr4, R-1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",R-1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,,,,,,,,\"R-1-(1-naphthyl)ethylamine, PbBr2\",R-1-(1-naphthyl)ethylammonium lead bromide,\"A hot solution of PbBr2 (45 mg, 0.12 mmol) and R-1-(1-naphthyl)ethylamine (39 µL, 0.24 mmol ) in 0.5 ml aq. HBr and 1.2 ml deionized water in a sealed vial with an N2 atmosphere was slowly cooled from 95 °C to room temperature over 48 hr. The colorless, plate-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-020-18485-7,S-1-methyl benzylamine lead iodide,C16H24N2PbI4,\"S-MBA2PbI4, S-MBPI, (S)-Œ±-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",S-1-methyl benzylaminium lead (II) iodide,2,single crystal,,,,,,,,\"(S)-(−)-α-methyl benzylamine, PbI2\",(S)-(−)-α-methyl benzylammonium lead iodide (S-MBA2PbI4),\"Single crystals of S-MBPI were grown by slowly evaporating a solution of (S)-(−)-α-methyl benzylamine (25 µL, 0.2 mmol) and PbI2 (45 mg, 0.1 mmol) in 1 ml aq. HI and 1 ml methanol at room temperature under N2 atmosphere. The orange-red, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-020-18485-7,S-1-methyl benzylamine lead iodide,C16H24N2PbI4,\"S-MBA2PbI4, S-MBPI, (S)-Œ±-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",S-1-methyl benzylaminium lead (II) iodide,2,single crystal,,,,,,,,\"(S)-(−)-α-methyl benzylamine, PbI2\",(S)-(−)-α-methyl benzylammonium lead iodide (S-MBA2PbI4),\"Single crystals of S-MBPI were grown by slowly evaporating a solution of (S)-(−)-α-methyl benzylamine (25 µL, 0.2 mmol) and PbI2 (45 mg, 0.1 mmol) in 1 ml aq. HI and 1 ml methanol at room temperature under N2 atmosphere. The orange-red, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 200 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-020-18485-7,S-1-methyl benzylamine lead iodide,C16H24N2PbI4,\"S-MBA2PbI4, S-MBPI, (S)-Œ±-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",S-1-methyl benzylaminium lead (II) iodide,2,single crystal,,,,,,,,\"(S)-(−)-α-methyl benzylamine, PbI2\",(S)-(−)-α-methyl benzylammonium lead iodide (S-MBA2PbI4),\"Single crystals of S-MBPI were grown by slowly evaporating a solution of (S)-(−)-α-methyl benzylamine (25 µL, 0.2 mmol) and PbI2 (45 mg, 0.1 mmol) in 1 ml aq. HI and 1 ml methanol at room temperature under N2 atmosphere. The orange-red, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 100 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-020-18485-7,1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,,,,,,,,\"1-(1-naphthyl)ethylamine (98%), PbBr2\",1-(1-naphthyl)ethylammoium lead bromide,\"A hot solution of 1-(1-naphthyl)ethylamine (39 µL, 0.24 mmol ) and PbBr2 (45 mg, 0.12 mmol) in 0.5 ml of aq. HBr and 1.2 ml methanol is cooled from 95 °C to room temperature over 48 hr. The colorless plate-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Bruker APEX II CCD diffractometer using Mo-Kα radiation (λ=0.710 Å) and X-ray tube operating at 50 kV and 30 mA\r\n10.1038/s41467-020-18485-7,S-1-(1-naphthyl)ethylammonium lead iodide,C24H28N2Pb2I6,\"S-NEA2Pb2I6, S-C24H28N2Pb2I6, S-NPI, S-1-(1-naphthyl)ethylammonium hexaiodo diplumbate(II)\",C12H14N,\"Pb2I6, Lead iodide\",S-1-(1-naphthyl)ethanaminium lead iodide,1,single crystal,,,,,,,,\"(S)-(−)-1-(1-naphthyl)ethylamine (≥99%), PbI2\",S-NEA2Pb2I6 (S-NPI),\"Single crystals of 1D S-NEA2Pb2I6 (S-NPI) were obtained by cooling a hot aq. HI solution of S-1-(1-naphthyl)ethylamine (0.25 mmol) and PbI2 (0.125 mmol) from  90 °C to room-temperature in 48 hr. The pale-yellow, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Bruker APEX II CCD diffractometer using Mo-Kα radiation (λ=0.710 Å) and X-ray tube operating at 50 kV and 30 mA\r\n10.1038/s41467-020-18485-7,1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,FHI-aims,DFT,PBE,2×4×4,atomic ZORA,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,S-1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"S-NEA2PbBr4, S-1-(1-naphthyl)ethanaminium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",S-1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,FHI-aims,DFT,PBE,2×4×4,atomic ZORA,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,S-1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"S-NEA2PbBr4, S-1-(1-naphthyl)ethanaminium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",S-1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,FHI-aims,DFT,HSE06,3×4×4,atomic ZORA with SOC,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,R-1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"R-NEA2PbBr4, R-1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",R-1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,FHI-aims,DFT,PBE,2×4×4,atomic ZORA,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,R-1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"R-NEA2PbBr4, R-1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",R-1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,FHI-aims,DFT,HSE06,3×4×4,atomic ZORA with SOC,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,FHI-aims,DFT,PBE,2×4×4,atomic ZORA,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,1-(1-naphthyl)ethylammonium lead bromide,C24H28N2PbBr4,\"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",C12H14N,\"PbBr4, Lead bromide\",1-(1-naphthyl)ethanaminium lead (II) bromide,2,single crystal,FHI-aims,DFT,HSE06,3×4×4,atomic ZORA with SOC,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,S-1-methyl benzylamine lead iodide,C16H24N2PbI4,\"S-MBA2PbI4, S-MBPI, (S)-Œ±-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",S-1-methyl benzylaminium lead (II) iodide,2,single crystal,FHI-aims,DFT,PBE,2×4×4,atomic ZORA,NAO,,,,,,\r\n10.1038/s41467-020-18485-7,S-1-methyl benzylamine lead iodide,C16H24N2PbI4,\"S-MBA2PbI4, S-MBPI, (S)-Œ±-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",S-1-methyl benzylaminium lead (II) iodide,2,single crystal,FHI-aims,DFT,HSE06,3×4×4,atomic ZORA with SOC,NAO,,,,,,\r\n10.1038/s41467-021-25149-7,R-4-Cl-MBA2PbBr4,(C8H11ClN)2PbBr4,\"(R)-4-chloro-Œ±-methylbenzylammonium lead bromide, (R)-1-(4-chlorophenyl)ethylammonium lead bromide, (R)-1-(4-chlorophenyl)ethylammonium tetrabromoplumbate(II)\",C8H11ClN,\"PbBr4, Lead bromide\",None,2,single crystal,,,,,,,,\"(R)-4-chloro-a-methylbenzylamine (97%), PbBr2, Aq. HBr (48 wt.% in H2O, ≥ 99.99%)\",R-4-Cl-MBA2PbBr4,\"Plate-like, colorless crystals were grown by slowly cooling a hot Aq. HBr solution of 0.122 mol of PbBr2 and 0.244 mmol of organic amine from 95ºC to room temperature over 60 hours. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and an X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-021-25149-7,S-1-Me-HA2PbI4,(C7H18N)2PbI4,\"(S)-1-methylhexylammonium lead iodide, (S)-1-methylhexylammonium tetraiodoplumbate(II)\",C7H18N,\"PbI4, Lead iodide\",None,2,single crystal,,,,,,,,\"(S)-(+)-1-methyl hexylamine or (S)-(+)-2-Aminoheptane (99%), PbI2, Aq. HI (57 wt. % in H2O, distilled, stabilized, 99.95%)\",S-1-Me-HA2PbI4,\"Orange crystals were grown by slowly cooling a hot Aq. HI solution of 0.122 mol of PbI2 and 0.244 mmol of organic amine from 95ºC to room temperature over 60 hours. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and an X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-021-25149-7,S-2-Me-BuA2PbBr4,(C5H14N)2PbBr4,\"(S)-2-methylbutylammonium lead bromide, (S)-2-methylbutylammonium tetrabromoplumbate(II)\",C5H14N,\"PbBr4, Lead bromide\",None,2,single crystal,,,,,,,,\"(S)-(−)-2-Methylbutylamine (95%), PbBr2, Aq. HBr (48 wt.% in H2O, ≥ 99.99%)\",S-2-Me-BuA2PbBr4,\"Plate-like, colorless crystals were grown by slowly cooling a hot Aq. HBr solution of 0.122 mol of PbBr2 and 0.244 mmol of organic amine from 95ºC to room temperature over 60 hours. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and an X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-021-25149-7,S-4-NO2-MBA2PbBr4.H2O,(C8H11N2O2)2PbBr4.H2O,\"(S)-Œ±-Methyl-4-nitrobenzylammonium lead bromide, (S)-4-nitro-Œ±-methylbenzylammonium lead bromide, (S)-4-nitro-Œ±-methylbenzylammonium tetrabromoplumbate(II)\",C8H11N2O2,\"PbBr4, Lead bromide\",None,2,single crystal,,,,,,,,\"(S)-α-Methyl-4-nitrobenzylamine hydrochloride or (S)-4-nitro-α-methylbenzylamine hydrochloride [‘S-4-NO2-MBA∙HCl’, 97%], PbBr2,  Aq. HBr (48 wt.% in H2O, ≥ 99.99%)\",S-4-NO2-MBA2PbBr4.H2O,\"Plate-like, colorless single-crystals of [S-4-NO2-MBA]2PbBr4 were grown by slowly evaporating a solution of 0.122 mmol of PbBr2 and 0.244 mmol of S-4-NO2-MBA∙HCl in 0.5 ml Aq. HBr and 1.7 ml methanol at room temperature in the ambient atmosphere.\",Single crystal X-ray diffraction,Single-crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and an X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41467-021-25149-7,S-4-NH3-MBAPbI4,(C8H14N2)PbI4,\"(S)-4-ammonio-Œ±-methylbenzylammonium lead iodide, (S)-4-ammonio-Œ±-methylbenzylammonium tetraiodoplumbate(II)\",C8H14N2,\"PbI4, Lead iodide\",None,2,single crystal,,,,,,,,\"(S)-α-Methyl-4-nitrobenzylamine hydrochloride (97%), PbI2, Aq. HI (57 wt. % in H2O, distilled, stabilized, 99.95%), Aq. H3PO2 (50 wt.% in H2O)\",S-4-NH3-MBA2PbI4,\"Single-crystals of S-4-NH3-MBAPbI4 were grown by slowly cooling a hot solution of 0.245 mmol of PbI2, and 0.49 mmol of S-4-NO2-MBA∙HCl in 0.2 ml of Aq. HI and 0.1 ml of Aq. H3PO2  from 85°C to room temperature over 5 hrs. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",Single crystal X-ray diffraction,Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-Kα radiation (λ=0.710 Å) and an X-ray tube operating at 50 kV and 30 mA.\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumbithiophene) lead iodide,C20H24N2S4PbI4,\"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",C10H12NS2,\"PbI4, Lead iodide\",\"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",2,film,,,,,,,,\"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. 2T (100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film forms after the solvent dry off.\",Steady-state Photoluminescence,A home-built confocal micro-photoluminescence setup was used to record the PL spectrum.\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumbithiophene) lead iodide,C20H24N2S4PbI4,\"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",C10H12NS2,\"PbI4, Lead iodide\",\"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",2,film,,,,,,,,\"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. 2T (100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film forms after the solvent dry off.\",Steady-state Photoluminescence,A home-built confocal micro-photoluminescence setup was used to record the PL spectrum.\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumdimethylquaterthiophene) lead iodide,C40H40N2S8PbI4,\"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) ¬∑I3Pb¬∑I, 5-ethanaminium-4',3'''dimethyl-2,2‚Äò:5‚Äò,2‚Äò‚Äò:5‚Äò‚Äò,2‚Äò‚Äò‚Äò-quaterthiophene tetraiodoplumbate(II)\",C20H20NS4,\"PbI4, Lead iodide\",\"5-ethanaminium-4',3'''dimethyl-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tin iodide\",2,single crystal,,,,,,,,\"As-synthesized 4Tm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2\",orange plate-like crystals,\"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 4Tm (10.6 mg, 20  µmol) and PbI2(4.6 mg, 10 µmol) were dissolved in a mixture of DMF (1 mL) and CB (1 mL). \r\nTo obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",Single Crystal X-Ray Diffraction,\"Data were collected using a Bruker AXS D8 Quest CMOS diffractometer, an I-mu-S microsource X-ray tube with Cu Kα radiation (λ = 1.54178 Å), Goebel mirror, and a Photon2 CMOS area detector. Data was collected and analyzed at 150 K. Files were scaled and corrected using APEX3.\"\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumdimethylquaterthiophene) lead iodide,C40H40N2S8PbI4,\"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) ¬∑I3Pb¬∑I, 5-ethanaminium-4',3'''dimethyl-2,2‚Äò:5‚Äò,2‚Äò‚Äò:5‚Äò‚Äò,2‚Äò‚Äò‚Äò-quaterthiophene tetraiodoplumbate(II)\",C20H20NS4,\"PbI4, Lead iodide\",\"5-ethanaminium-4',3'''dimethyl-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tin iodide\",2,film,,,,,,,,\"As-synthesized 4Tm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2\",orange crystals,\"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 4Tm (10.6 mg, 20 µmol) and PbI2(4.6 mg, 10 µmol) were dissolved in a mixture of DMF (1 mL) and CB (1 mL). Afterward, the solution was diluted 60 times with acetonitrile/chlorobenzene (1:2:5 volume ratio). The solution was diluted 5 more times with either CB or CB/acetonitrile (3:1 volume ratio). Next, the Si/SiO2 substrates were then cleaned via ultrasonication in isopropanol, water, acetone, and isopropanol again. Substrates were dried by a nitrogen gun, transported into the glove box, and preheated to 80º C. The prepared, diluted solution was then dropped onto the Si/SiO2 substrate, 10 mL at a time, and dried at 80ºC. Thin sheets of (4Tm)2PbI4 grew spontaneously within 10 minutes. To obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.,\"Absorption correction was performed with Multi-scan SADABS 2016/2: Krause, L., Herbst-Irmer, R., Sheldrick G.M. & Stalke D., J. Appl. Cryst. 48 (2015) 3-10.\"\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumdimethylquaterthiophene) lead iodide,C40H40N2S8PbI4,\"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) ¬∑I3Pb¬∑I, 5-ethanaminium-4',3'''dimethyl-2,2‚Äò:5‚Äò,2‚Äò‚Äò:5‚Äò‚Äò,2‚Äò‚Äò‚Äò-quaterthiophene tetraiodoplumbate(II)\",C20H20NS4,\"PbI4, Lead iodide\",\"5-ethanaminium-4',3'''dimethyl-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tin iodide\",2,film,,,,,,,,\"As-synthesized 4Tm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. 4Tm (53.0 mg, 100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed at 200 °C on a hot plate for 10 min.\",Ultraviolet photoelectron spectroscopy (UPS) + Cyclic voltametry (CV),UPS was recorded using Kratos Axis Ultra DLD spectrometer with He I radiation (21.2 eV) at pass energy (PE) of 5 eV. CV was recorded using a CHI660 electrochemical analyzer.\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumbithiophene) lead iodide,C20H24N2S4PbI4,\"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",C10H12NS2,\"PbI4, Lead iodide\",\"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",2,film,,,,,,,,\"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. 2T (100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film forms after the solvent dry off.\",UV-vis absorption,Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumdimethylquaterthiophenecarbonitrile) lead iodide,C40H36N6S8PbI4,\"(4TCNm)2PbI4, (C20H18N3S4)2PbI4, 5-ethanaminium-4',3'''dimethyl-2,2‚Äò:5‚Äò,2‚Äò‚Äò:5‚Äò‚Äò,2‚Äò‚Äò‚Äò-quaterthiophene-3'',4''-dicarbonitrile tetraiodoplumbate(II) \",C20H18N3S4,\"PbI4, Lead iodide\",\"5-ethanaminium-4',3'''dimethyl-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene-3'',4''-dicarbonitrile\",2,film,,,,,,,,\"As-synthesized 4TCNm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. 4TCNm (100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed at 180 °C on a hot plate for 10 min.\",Ultraviolet photoelectron spectroscopy (UPS) + Cyclic voltametry (CV),UPS was recorded using Kratos Axis Ultra DLD spectrometer with He I radiation (21.2 eV) at pass energy (PE) of 5 eV. CV was recorded using a CHI660 electrochemical analyzer.\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumdimethylquaterthiophenecarbonitrile) lead iodide,C40H36N6S8PbI4,\"(4TCNm)2PbI4, (C20H18N3S4)2PbI4, 5-ethanaminium-4',3'''dimethyl-2,2‚Äò:5‚Äò,2‚Äò‚Äò:5‚Äò‚Äò,2‚Äò‚Äò‚Äò-quaterthiophene-3'',4''-dicarbonitrile tetraiodoplumbate(II) \",C20H18N3S4,\"PbI4, Lead iodide\",\"5-ethanaminium-4',3'''dimethyl-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene-3'',4''-dicarbonitrile\",2,film,,,,,,,,\"As-synthesized 4TCNm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2\",Yellow solid,\"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 4TCNm (10.6 mg, 20 µmol) and PbI2(4.6 mg, 10 µmol) were dissolved in a mixture of DMF (1 mL) and CB (1 mL). Afterward, the solution was diluted 60 times with acetonitrile/chlorobenzene (1:2:5 volume ratio). The solution was diluted 5 more times with either CB or CB/acetonitrile (3:1 volume ratio). Next, the Si/SiO2 substrates were then cleaned via ultrasonication in isopropanol, water, acetone, and isopropanol again. Substrates were dried by a nitrogen gun, transported into the glove box, and preheated to 80º C. The prepared, diluted solution was then dropped onto the Si/SiO2 substrate, 10 mL at a time, and dried at 80ºC. Thin sheets of (4TCNm)2PbI4 grew spontaneously within 10 minutes. Thin polycrystalline films were annealed at 100º. Though the organic ligand was too large (and approaching the extent of the perovskite’s lattice), a yellow solid product resulted.\",Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.,\"Absorption correction was performed with Multi-scan SADABS 2016/2: Krause, L., Herbst-Irmer, R., Sheldrick G.M. & Stalke D., J. Appl. Cryst. 48 (2015) 3-10.\"\r\n10.1038/s41557-019-0354-2,bis(BTm) lead iodide,C24H22NS4PbI4,\"(BTm)2PbI4, I8Pb2¬∑4(C24H22NS4), (BTm)2PbI4\",C24H22NS4,\"PbI4, Lead iodide\",\"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",2,film,,,,,,,,\"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. BTm (100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed on a hot plate for 10 min.\",Ultraviolet photoelectron spectroscopy (UPS) + Cyclic voltametry (CV),UPS was recorded using Kratos Axis Ultra DLD spectrometer with He I radiation (21.2 eV) at pass energy (PE) of 5 eV. CV was recorded using a CHI660 electrochemical analyzer.\r\n10.1038/s41557-019-0354-2,bis(BTm) lead iodide,C24H22NS4PbI4,\"(BTm)2PbI4, I8Pb2¬∑4(C24H22NS4), (BTm)2PbI4\",C24H22NS4,\"PbI4, Lead iodide\",\"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",2,film,,,,,,,,\"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. BTm (100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed on a hot plate for 10 min.\",UV-vis absorption,Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.\r\n10.1038/s41557-019-0354-2,bis(BTm) lead iodide,C24H22NS4PbI4,\"(BTm)2PbI4, I8Pb2¬∑4(C24H22NS4), (BTm)2PbI4\",C24H22NS4,\"PbI4, Lead iodide\",\"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",2,film,,,,,,,,\"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",Thin film,\"The entire procedure was performed inside a nitrogen-filled glove box. BTm (100 μmol) and PbI2 (23.0 mg, 50 μmol) were dissolved in 0.25 mL of anhydrous DMF at 70 °C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed on a hot plate for 10 min.\",Steady-state Photoluminescence,A home-built confocal micro-photoluminescence setup was used to record the PL spectrum.\r\n10.1038/s41557-019-0354-2,bis(BTm) lead iodide,C24H22NS4PbI4,\"(BTm)2PbI4, I8Pb2¬∑4(C24H22NS4), (BTm)2PbI4\",C24H22NS4,\"PbI4, Lead iodide\",\"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",2,single crystal,,,,,,,,\"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl)\",red plates,\"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized BTm (10.6 mg, 20  µmol) and PbI2(4.6 mg, 10 µmol) were dissolved in a mixture of DMF (1 mL). To obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",Single Crystal X-Ray Diffraction,\"Data were collected using a Bruker AXS D8 Quest CMOS diffractometer with PhotonII charge-integrating pixel array detector (CPAD), an I-µ-S microsource X-ray tube (Cu K???? radiation, ????=1.54178 Å), Goebel mirror, and a Photon2 CMOS area detector. Data was collected and analyzed at 150 K. Files were scaled and corrected using APEX3.\"\r\n10.1038/s41557-019-0354-2,Bis(ethylammoniumbithiophene) lead iodide,C20H24N2S4PbI4,\"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",C10H12NS2,\"PbI4, Lead iodide\",\"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",2,single crystal,,,,,,,,\"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl)\",orange-red plates,\"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 2T (10.6 mg, 20  µmol) and PbI2(4.6 mg, 10 µmol) were dissolved in a mixture of DMF (1 mL).\r\n\r\nTo obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",Single Crystal X-Ray Diffraction,\"Data was collected via a Bruker AXS D8 Quest diffractometer, a sealed tube X-ray radiation source with Mo Kα radiation (λ = 0.71073 Å), and a triumph curved graphite crystal monochromator. Data was collected and analyzed at 150 K. Files were scaled and corrected using APEX3.\"\r\n10.1038/s41557-020-0488-2,Bis(naphthaleneoxybutylammonium) lead iodide,\"(C14H18ON)2PbI4, C28H36O2N2PbI4\",\"(Nap-O-Bu-NH3)2PbI4, (naphthalene-O-butyl-NH3)2PbI4, bis(naphthaleneoxybutylaminium) tetraiodoplumbate(II)\",C14H18ON,\"PbI4, Lead iodide\",bis(naphthaleneoxybutylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",Plate-like crystals,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\"\r\n10.1038/s41557-020-0488-2,Bis(naphthaleneoxyhexylammonium) lead iodide,(C16H22ON)2PbI4,\"(Nap-O-Hex-NH3)2PbI4, (naphthalene-O-hexyl-NH3)2PbI4, bis(naphthaleneoxyhexylaminium) tetraiodoplumbate(II)\",C16H22ON,\"PbI4, Lead iodide\",bis(naphthaleneoxyhexylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",Plate-like crystals,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\"\r\n10.1038/s41557-020-0488-2,Bis(5-methoxynaphthaleneoxyethylammonium) lead iodide,(C13H16O2N)2PbI4,\"(MeO-Nap-O-Et-NH3)2PbI4, (methoxy-naphthalene-O-ethyl-NH3)2PbI4, bis(methoxynaphthaleneoxyethylaminium) tetraiodoplumbate(II)\",C13H16O2N,\"PbI4, Lead iodide\",bis(5-methoxynaphthaleneoxyethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",Plate-like crystals,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\"\r\n10.1038/s41557-020-0488-2,Bis(5-methoxynaphthaleneoxybutylammonium) lead iodide,(C15H20O2N)2PbI4,\"(MeO-Nap-O-Bu-NH3)2PbI4, (methoxy-naphthalene-O-butyl-NH3)2PbI4, bis(methoxynaphthaleneoxybutylaminium) tetraiodoplumbate(II)\",C15H20O2N,\"PbI4, Lead iodide\",bis(5-methoxynaphthaleneoxybutylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",Plate-like crystals,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter.  100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\"\r\n10.1038/s41557-020-0488-2,Bis(5-methoxynaphthaleneoxyhexylammonium) lead iodide,(C17H24O2N)2PbI4,\"(MeO-Nap-O-Hex-NH3)2PbI4, (methoxy-naphthalene-O-hexyl-NH3)2PbI4, bis(methoxynaphthaleneoxyhexylaminium) tetraiodoplumbate(II)\",C17H24O2N,\"PbI4, Lead iodide\",bis(5-methoxynaphthaleneoxyhexylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",Plate-like crystals,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\"\r\n10.1038/s41557-020-0488-2,Bis(pentachloro-phenyloxypropylammonium) lead iodide,(Cl5C9H9ON)2PbI4,\"(C6Cl5-O-Pr-NH3)2PBI4, (C6Cl5-O-propyl-NH3)2PbI4, bis(pentachloro-phenyloxypropylaminium) tetraiodoplumbate(II)\",Cl5C9H9ON,\"PbI4, Lead iodide\",bis(pentachloro-phenyloxypropylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",Plate-like crystals,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",Single-crystal X-ray diffraction,\"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\"\r\n10.1038/s41557-020-0488-2,Bis(5-methoxynaphthaleneoxyethylammonium) lead iodide,(C13H16O2N)2PbI4,\"(MeO-Nap-O-Et-NH3)2PbI4, (methoxy-naphthalene-O-ethyl-NH3)2PbI4, bis(methoxynaphthaleneoxyethylaminium) tetraiodoplumbate(II)\",C13H16O2N,\"PbI4, Lead iodide\",bis(5-methoxynaphthaleneoxyethylaminium) lead (II) iodide,2,film,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours. The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\r\n10.1038/s41557-020-0488-2,Bis(5-methoxynaphthaleneoxybutylammonium) lead iodide,(C15H20O2N)2PbI4,\"(MeO-Nap-O-Bu-NH3)2PbI4, (methoxy-naphthalene-O-butyl-NH3)2PbI4, bis(methoxynaphthaleneoxybutylaminium) tetraiodoplumbate(II)\",C15H20O2N,\"PbI4, Lead iodide\",bis(5-methoxynaphthaleneoxybutylaminium) lead (II) iodide,2,film,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.  The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\r\n10.1038/s41557-020-0488-2,Bis(5-methoxynaphthaleneoxyhexylammonium) lead iodide,(C17H24O2N)2PbI4,\"(MeO-Nap-O-Hex-NH3)2PbI4, (methoxy-naphthalene-O-hexyl-NH3)2PbI4, bis(methoxynaphthaleneoxyhexylaminium) tetraiodoplumbate(II)\",C17H24O2N,\"PbI4, Lead iodide\",bis(5-methoxynaphthaleneoxyhexylaminium) lead (II) iodide,2,film,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours. The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\r\n10.1038/s41557-020-0488-2,Bis(pentachloro-phenyloxypropylammonium) lead iodide,(Cl5C9H9ON)2PbI4,\"(C6Cl5-O-Pr-NH3)2PBI4, (C6Cl5-O-propyl-NH3)2PbI4, bis(pentachloro-phenyloxypropylaminium) tetraiodoplumbate(II)\",Cl5C9H9ON,\"PbI4, Lead iodide\",bis(pentachloro-phenyloxypropylaminium) lead (II) iodide,2,film,,,,,,,,\"Dichloromethane (DCM), γ-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",Thin film on glass substrate,\"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in γ-butyrolactone. The solution was filtered through a 0.45-µm polytetrafluoroethylene filter. 100 µl of the filtrate was taken in a 1.5 ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours. The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",UV-vis absorption,A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\r\n10.1038/s41563-018-0081-x,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"PbBr2, PEABr, DMF, DMSO, Diethyl Ether, Chloroform\",(PEA)2PbBr4 single crystal,\"PbBr2 and PEABr with molar ratio of 1:2 were dissolved into a mixed solvent of DMF and DMSO (30-60%) in a 20ml vial. The vial was put in a sealed larger vail with 40 ml antisolvent (diethyl ether or chloroform). After several days at room temperature, single crystal  (PEA)2PbBr4 will be obtianed, which was rinsed with antisolvent for 3 times and dried at vacuum.\",Single crystal X-ray diffraction,A P4 Bruker diffractometer with Bruker SMART 1 K CCD (charge-coupled device) detector and a rotating anode utilizing Mo KR radiation (λ = 0.710 73 Å) was used to measure  SCXRD data. OLEX2 was used to fitting refinement of single-crystal structures.\r\n10.1038/s41563-018-0081-x,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"PbBr2, PEABr, DMF, DMSO, Diethyl Ether, Chloroform\",(PEA)2PbBr4 single crystal,\"PbBr2 and PEABr with molar ratio of 1:2 were dissolved into a mixed solvent of DMF and DMSO (30-60%) in a 20ml vial. The vial was put in a sealed larger vail with 40 ml antisolvent (diethyl ether or chloroform). After several days at room temperature, single crystal  (PEA)2PbBr4 will be obtianed, which was rinsed with antisolvent for 3 times and dried at vacuum.\",Single crystal X-ray diffraction,A P4 Bruker diffractometer with Bruker SMART 1 K CCD (charge-coupled device) detector and a rotating anode utilizing Mo KR radiation (λ = 0.710 73 Å) was used to measure  SCXRD data. OLEX2 was used to fitting refinement of single-crystal structures.\r\n10.1038/s41586-020-2219-7,Bis(ethylammoniumbithiophene) tin iodide,(2T)2SnI4,\"(2T)2SnI4, bis(ethylammoniumbithiophene) tetraiodostannate(II)\",C5H7NS,\"SnI4, Tin iodide\",bis(ethylammoniumbithiophene) tin iodide,2,nanoform,,,,,,,,\"2T•HI(2T: bithiophenylethylammonium), tin iodide (SnI2), dimethylformide (DMF), anhydrous chlorobenzene (CB), SiO2 (300 nm)/Si substrates\",<5 layers thick crystal,The process was carried out inside an N2-filled glovebox. 10 μmol of SnI2 and 20 μmol of 2T.HI were dissolved in 2 ml of DMF/CB co-solvent (1:1 v/v). The stock solution was then diluted 120 times by CB/AN/DCB co-solvent (2.5:1:0.01 volume ratio). 5–10 μl of the diluted solution was added onto the pre-cleaned substrate. CB vapor was allowed to be diffused at 70 °C for 10-30 min.,Photoluminescence,The PL spectrum was recorded using the SpectraPro HRS-300 spectrometer.\r\n10.1038/s41586-020-2219-7,Bis(ethylammoniumbithiophene) lead iodide,C20H24N2S4PbI4,\"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",C10H12NS2,\"PbI4, Lead iodide\",\"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",2,single crystal,,,,,,,,\"2T•HI(2T: bithiophenylethylammonium), lead iodide (PbI2), dimethylformide (DMF), anhydrous chlorobenzene (CB)\",sheet-like crystals,\"10 μmol of PbI2 and 20 μmol of 2T•HI were dissolved in 2 mL of DMF/CB co-solvent (1:1 ration). This resulted in 5 mM of stock solution. This solution was diluted 120 times by CB/An/DCB cosolvent (9.5:1:0.01 volume ratio). Only 5-10 μmol was placed on a growth substrate SiO2, at the bottom of a glass vial and was later transferred to another vial with 3 mL of CB. This was placed on a 70º hot plate. Growth took 10-30 minutes.\",Single Crystal X-Ray Diffraction,\"Bruker AXS D8 Quest CMOS diffractometer with kappa geometry, an I-μ-S microsource X-ray tube, multilayer Göbel mirror, and Photon2 CMOS was used. Data was collected with Cu Kα radiation (λ = 1.54178 Å).\"\r\n10.1038/s41586-020-2219-7,Bis(bithiophenylethylammonium) lead bromide,Br8Pb2•4(C10H12NS2),\"(2T)2PbBr4, bis(bithiophenylethylammonium) tetrabromoplumbate(II)\",C5H7NS,\"PbBr4, Lead bromide\",bis(bithiophenylethylammonium) lead (II) bromide,2,single crystal,,,,,,,,\"2T•HBr (2T: bithiophenylethylammonium), lead bromide (PbBr2), dimethylformide (DMF), anhydrous chlorobenzene (CB)\",sheet-like crystals,\"10 μmol of PbBr2 and 20 μmol of 2T•HBr were dissolved in 2 mL of DMF/CB co-solvent (1:1 ratio). This resulted in 5 mM of stock solution. This solution was diluted 120 times by CB/An/DCB cosolvent (2.5:1:0.01 volume ratio). Only 5-10 μmol was placed on a growth substrate SiO2, at the bottom of a glass vial and was later transferred to another vial with 3 mL of CB. This was placed on a 70º hot plate. Growth took 10-30 minutes.\",Single Crystal X-Ray Diffraction,\"Bruker AXS D8 Quest CMOS diffractometer with kappa geometry, an I-μ-S microsource X-ray tube, multilayer Göbel mirror, and Photon2 CMOS was used. Data was collected with Cu Kα radiation (λ = 1.54178 Å).\"\r\n10.1038/s41586-020-2219-7,Bis(ethylammoniumdimethylquaterthiophene) lead iodide,C40H40N2S8PbI4,\"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) ¬∑I3Pb¬∑I, 5-ethanaminium-4',3'''dimethyl-2,2‚Äò:5‚Äò,2‚Äò‚Äò:5‚Äò‚Äò,2‚Äò‚Äò‚Äò-quaterthiophene tetraiodoplumbate(II)\",C20H20NS4,\"PbI4, Lead iodide\",\"5-ethanaminium-4',3'''dimethyl-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tin iodide\",2,single crystal,,,,,,,,\"4Tm•HI(4Tm: quaterthiophenylethylammonium), lead iodide (PbI2), dimethylformide (DMF), anhydrous chlorobenzene (CB)\",sheet-like crystals,\"10 μmol of PbI2 and 20 μmol of 4Tm•HI were dissolved in 2 mL of DMF/CB co-solvent (1:1 ration). This resulted in 5 mM of stock solution. This solution was diluted 240 times by CB/An/DCB cosolvent (3.9:1:0.01 volume ratio). Only 5-10 μmol was placed on a growth substrate SiO2, at the bottom of a glass vial and was later transferred to another vial with 3 mL of CB. This was placed on a 90º hot plate. Growth took 10-30 minutes.\",Single Crystal X-Ray Diffraction,\"Bruker AXS D8 Quest CMOS diffractometer with kappa geometry, an I-μ-S microsource X-ray tube, multilayer Göbel mirror, and Photon2 CMOS was used. Data was collected with Cu Kα radiation (λ = 1.54178 Å).\"\r\n10.1038/s41598-019-49926-z,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,single crystal,,,,,,,,\"Lead chloride (PbCl2, 99.999%, Alfa Aesar), methylammonium hydrochloride (CH3NH3Cl, 99%, Alfa Aesar), dimethylformamide (DMF) (C3H7NO, 99.5%, Merck KGaA), and dimethyl sulfoxide (DMSO) (C2H6OS, 99.7%, Sigma-Aldrich)\",MAPbCl3 single crystals of size ~2.5 mm × 2 mm × 1 mm,\"0.2228 gm of CH3NH3Cl was dissolved in a 3.3 mL DMSO: DMF (1:1) solution using an ultrasonic bath for 10 minutes under an N2 atmosphere at room temperature. In 3 mL of the prepared CH3NH3Cl/DMSO:DMF (1:1) solution, 0.8343 g PbCl2 was added. The mixture was stirred for 20 min until the solution becomes transparent. The solution was filtered using PVDF filter. The filtrate was transferred in a vial and kept in an oil bath undisturbed at 50 °C for 6 ~8 h. After the formation of the crystals, they were dried with a nitrogen gun.\",Photoluminescence measurement at 300 K,\"PL spectrum was recorded with a HORIBA iHR-550 spectrometer, liquid-nitrogen cooled CCD detector, and semiconductor laser operated at 266 nm.\"\r\n10.1038/s41598-019-49926-z,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,single crystal,,,,,,,,\"Lead chloride (PbCl2, 99.999%, Alfa Aesar), methylammonium hydrochloride (CH3NH3Cl, 99%, Alfa Aesar), dimethylformamide (DMF) (C3H7NO, 99.5%, Merck KGaA), and dimethyl sulfoxide (DMSO) (C2H6OS, 99.7%, Sigma-Aldrich)\",MAPbCl3 single crystals of size ~2.5 mm × 2 mm × 1 mm,\"0.2228 gm of CH3NH3Cl was dissolved in a 3.3 mL DMSO: DMF (1:1) solution using an ultrasonic bath for 10 minutes under an N2 atmosphere at room temperature. In 3 mL of the prepared CH3NH3Cl/DMSO:DMF (1:1) solution, 0.8343 g PbCl2 was added. The mixture was stirred for 20 min until the solution becomes transparent. The solution was filtered using PVDF filter. The filtrate was transferred in a vial and kept in an oil bath undisturbed at 50 °C for 6 ~8 h. After the formation of the crystals, they were dried with a nitrogen gun.\",UV-Vis absorption,\"The spectrum was recorded using a combination of a HOROBA iHR-550 spectrometer, Xenon lamp, and liquid-nitrogen cooled CCD detector\"\r\n10.1038/s41598-019-49926-z,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,single crystal,,,,,,,,\"Lead chloride (PbCl2, 99.999%, Alfa Aesar), methylammonium hydrochloride (CH3NH3Cl, 99%, Alfa Aesar), dimethylformamide (DMF) (C3H7NO, 99.5%, Merck KGaA), and dimethyl sulfoxide (DMSO) (C2H6OS, 99.7%, Sigma-Aldrich)\",MAPbCl3 single crystals of size ~2.5 mm × 2 mm × 1 mm,\"0.2228 gm of CH3NH3Cl was dissolved in a 3.3 mL DMSO: DMF (1:1) solution using an ultrasonic bath for 10 minutes under an N2 atmosphere at room temperature. In 3 mL of the prepared CH3NH3Cl/DMSO:DMF (1:1) solution, 0.8343 g PbCl2 was added. The mixture was stirred for 20 min until the solution becomes transparent. The solution was filtered using PVDF filter. The filtrate was transferred in a vial and kept in an oil bath undisturbed at 50 °C for 6 ~8 h. After the formation of the crystals, they were dried with a nitrogen gun.\",Photoluminescence measurement at 300 K,\"PL spectrum was recorded with a HORIBA iHR-550 spectrometer, liquid-nitrogen cooled CCD detector, and semiconductor laser operated at 266 nm.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,VASP,DFT,PBE-GGA,7x5x7,Non-relativistic,Plane-wave with cutoff 900 eV,\"Tolerance for energy minimization 10e-9 eV/atom.\r\ninteratomic forces after relaxation were below 0.005 eV/Å, and the stresses were below 0.05 GPa\",,,,,\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,VASP,DFT,PBE-GGA,2x5x7,Non-relativistic,Plane-wave with cutoff 900 eV,Tolerance: 10e-9 eV,,,,,\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",Black d6-MAPbI3 powder,\"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \r\n\r\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \r\n\r\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 °C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",Neutron diffraction,\"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The sample size was ~5.5 g for the d6-MAPbI. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to SI: Supplementary Table 1 and Additional dataset; CCDC.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",Black d6-MAPbI3 powder,\"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI.\r\n\r\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box.\r\n\r\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 °C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",Neutron diffraction,\"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The sample size was ~5.5 g for the d6-MAPbI. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to SI: Supplementary Table 4 and Additional dataset; CCDC.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",Black d6-MAPbI3 powder,\"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \r\n\r\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \r\n\r\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 °C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",Neutron diffraction,\"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The sample size was ~5.5 g for the d6-MAPbI. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to SI: Supplementary Table 5.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CD3NH2 (Sigma-Aldrich, 99 atom % D)\",CD3NH3PbI3,\"The CD3NH3PbI3 was prepared using CD3NH2 that was 99 atom % D. \r\n\r\nSynthesis perovskite using a similar method as 4-a.\",Neutron diffraction,\"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to Additional dataset; CCDC.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CH3NH2, HI, D2O\",CH3ND3PbI3,\"Preparation of CH3ND3I:\r\nReact methylamine gas with HI to yield methyl ammonium iodide. Exchange the two H atoms attached to the nitrogen atoms with D by dissolving the salt in 10 ml D2O (99 atom % D), drying under vacuum, and then repeating two more times. The resulting CH3ND3I was estimated to be better than 98 atom% D on the ammonium group. \r\n\r\nSynthesis perovskite using a similar method as 4-a.\",Neutron diffraction,\"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to Additional dataset; CCDC.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",Black d6-MAPbI3 Powder,\"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \r\n\r\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \r\n\r\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 °C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",Neutron diffraction,\"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Heating and cooling rates were 1K/min. Refer to Page 10 Table 2.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",Black d6-MAPbI3 Powder,\"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \r\n\r\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \r\n\r\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 °C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",Synchrotron X-ray powder diffraction,\"The X-ray powder diffraction measurements were performed  on the bending magnet station at DND-CAT sector 5 of the Advanced Photon Source. The X-ray wavelength used was 0.40012(2) Å, selected to reduce X-ray absorption by the sample to an acceptable level. Temperatures were equilibrated for ~10 min after 1 K changes. Refer to Page 10 Table 2.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,CH3ND3I,Black CH3ND3PbI3 Powder,\"Preparation of CH3ND3I: React methylamine gas with HI to yield methyl ammonium iodide. Exchange the two H atoms attached to the nitrogen atoms with D by dissolving the salt in 10 ml D2O (99 atom % D), drying under vacuum, and then repeating two more times. The resulting CH3ND3I was estimated to be better than 98 atom% D on the ammonium group. \r\n\r\nAdd material to ~6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \r\n\r\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 °C for 1hr to remove residual solvent.\",Neutron diffraction,\"Samples were loaded into 8mm diameter vanadium cans in a helium glove-box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Heating and cooling rates were 1K/min. Refer to Page 10 Table 2.\"\r\n10.1038/srep35685,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,,Black MAPbI3 Powder,Not explicitly stated in article. But assume close to synthesis methods of the deuterated compounds. Refer to the related data sets.,Synchrotron X-ray powder diffraction,\"The X-ray powder diffraction measurements were performed  on the bending magnet station at DND-CAT sector 5 of the Advanced Photon Source. The X-ray wavelength used was 0.40012(2) Å, selected to reduce X-ray absorption by the sample to an acceptable level. Temperatures were equilibrated for ~10 min after 1 K changes. Refer to Page 10 Table 2.\"\r\n10.1039/A608415J,\"1,4-phenyldiammonium lead iodide tetrahydrofuran\",C6H10N2Pb2I6 3THF,\"1,4-benzenediaminium fluorolane bis(triiodoplumbate(II)), (C6H10N2)Pb2I6¬∑3THF\",C6H10N2,\"Pb2I6, Lead iodide\",\"1,4-benzenediaminium fluorolane lead iodide\",1,single crystal,,,,,,,,\"p-nitroaniline, PbI2, HI (aq)/acetonitrile, THF\",Orange parallelepiped crystals,\"React p-nitroaniline (0.59 g, 4.33 mmol) and lead(ii) iodide (1.00 g, 2.17 mmol) in 8 ml of concentrated 57 mass % aqueous hydriodic acid diluted with acetonitrile. Warm resulting solution to 60 °C and slowly cool to 20 °C during which the solution turns dark red-brown, and brown precipitate forms. Collect the precipitate and redissolve in tetrahydrofuran (THF) at 60 °C. Slowly cool the resulting solution from 60 to -10°C over 7 days.\",Single-crystal X-ray diffraction,\"Monochromated Mo-Ka radiation, a stream of dry N2 gas at -50 °C.\"\r\n10.1039/B205543K,Bis(2-thienylmethylammonium) methylammonium lead iodide,C11H22N3SPb2I7,\"(C4H3SCH2NH3)2(CH3NH3)Pb2I7, bis(2-thienylmethanaminium) methanaminium septaiodo diplumbate(II)\",\"C5H8NS, CH6N\",\"Pb2I7, Lead iodide\",bis(2-thienylmethanaminium) methanaminium lead iodide,2,single crystal,,,,,,,,\"C4H3SCH2NH2, HI, PbI2\",Red plate-like crystals,\"Under an argon atmosphere, stoichiometric quantities of PbI2 (0.4 mmol) and C4H3SCH2NH2 were mixed in a concentrated HI solution (8 mL) by heating at 60 °C. Slow cooling of the solution, forms the crystals.\",Single crystal X-ray diffraction,Frames were collected using an Enraf Nonius CAD4 diffractometer and using Mo Kα (λ = 0.71073 Å) radiation.\r\n10.1039/B205543K,Bis(2-thienylmethylammonium) methylammonium lead iodide,C11H22N3SPb2I7,\"(C4H3SCH2NH3)2(CH3NH3)Pb2I7, bis(2-thienylmethanaminium) methanaminium septaiodo diplumbate(II)\",\"C5H8NS, CH6N\",\"Pb2I7, Lead iodide\",bis(2-thienylmethanaminium) methanaminium lead iodide,2,single crystal,,,,,,,,\"C4H3SCH2NH2, HI, PbI2\",Red plate-like crystals,\"Under an argon atmosphere, stoichiometric quantities of PbI2 (0.4 mmol) and C4H3SCH2NH2 were mixed in a concentrated HI solution (8 mL) by heating at 60 °C. Slow cooling of the solution, formed the crystals.\",Photoluminescence,\r\n10.1039/b406671e,\"1,4-phenylendiammonium copper chloride\",C6H10N2CuCl4,\"1,4-phenylendiaminium tetrachlorocuprate(II), (H2C6H4(NH2)2)CuCl4\",C6H10N2,\"CuCl4, Copper chloride\",\"1,4-phenylendiaminium copper (II) chloride\",2,single crystal,,,,,,,,\"1,4-Phenylenediamine, ethyl ether, CuCl2, HCl\",Small yellow plates,\"Dissolve 1,4-Phenylenediamine (18 mg, 0.17 mmol) in 2 ml of ethyl ether and layer on a solution of CuCl2 (13 mg, 0.10 mmol) dissolved in 5 mL concentrated hydrochloric acid. Allow for solvent diffusion over a period of several days.\",Single-crystal X-ray diffraction,Nonius KappaCCD diffractometer using graphite-monochromated Mo Kα radiation.\r\n10.1039/b406671e,\"1,4-phenylendiammonium lead chloride\",C6H10N2Pb2Cl6,\"1,4-phenylendiaminium trichloroplumbate(II), (H2C6H4(NH2)2)(PbCl3)2\",C6H10N2,\"PbCl3, Lead chloride\",\"1,4-phenylendiaminium lead (II) chloride\",1,single crystal,,,,,,,,\"1,4-Phenylenediamine, ethyl ether, PbCl2, HCl\",Colourless plates,\"Dissolve 1,4-Phenylenediamine (18 mg, 0.17 mmol) in 2 ml of ethyl ether and layer on a solution of PbCl2 (31 mg, 0.11 mmol) dissolved in 5 mL concentrated hydrochloric acid. Allow crystal formation after several days.\",Single-crystal X-ray diffraction,Nonius KappaCCD diffractometer using graphite-monochromated Mo Kα radiation.\r\n10.1039/b406671e,Bis(p-biphenylamine) copper chloride,C24H24N2CuCl4,\"bis(1,1'biphenyl-4-aminium) tetrachlorocuprate(II), (HC6H4(NH2)(C6H5))2CuCl4\",C12H12N,\"CuCl4, Copper chloride\",\"bis(1,1'biphenyl-4-aminium) copper (II) chloride\",2,single crystal,,,,,,,,\"CuCl2, HCl, ethyl ether, p-biphenylamine\",Pale yellow prisms,\"Dissolve CuCl2 (17 mg, 0.13 mmol) in 5 mL concentrated hydrochloric acid. Add a 2 ml ethyl ether solution of p-biphenylamine (16 mg, 0.10 mmol) as a top layer. Allow solvent diffusion over two weeks.\",Single-crystal X-ray diffraction,Nonius KappaCCD diffractometer using graphite-monochromated Mo Kα radiation.\r\n10.1039/b406671e,Benzidine copper chloride,C12H14N2CuCl4,\"1,1'-biphenyl-4,4'-diaminium tetrachlorocuprate(II), (H2(C6H4)2(NH2)2)CuCl4\",C12H14N2,\"CuCl4, Copper chloride\",\"1,1'-biphenyl-4,4'-diaminium copper (II) chloride\",2,single crystal,,,,,,,,\"CuCl2, HCl, ethyl ether, benzidine\",Pale yellow plates,\"Dissolve CuCl2 (25 mg, 0.19 mmol) in 8 mL concentrated hydrochloric acid. Add a 5 ml ethyl ether solution of benzidine (20 mg, 0.11 mmol) as a top layer. Allow solvent diffusion over several days.\",Single-crystal X-ray diffraction,Nonius KappaCCD diffractometer using graphite-monochromated Mo Kα radiation.\r\n10.1039/b406671e,Bis(benzidine) lead chloride,C24H28N4PbCl6,\"bis(1,1'-biphenyl-4,4'-diaminium) hexachloroplumbate(II), (H2(C6H4)2(NH2)2)2PbCl6\",C12H14N2,\"PbCl6, Lead chloride\",\"bis(1,1'-biphenyl-4,4'-diaminium) lead chloride\",0,single crystal,,,,,,,,\"PbCl2, HCl, ethyl ether, benzidine\",Colourless needles,\"Dissolve PbCl2 (55 mg, 0.20 mmol) in 8 mL concentrated hydrochloric acid. Add a 5 ml ethyl ether solution of benzidine (19 mg, 0.11 mmol) as a top layer. Allow solvent diffusion over several days.\",Single-crystal X-ray diffraction,Nonius KappaCCD diffractometer using graphite-monochromated Mo Kα radiation.\r\n10.1039/b606987h,bismethylbenzylammonium lead iodide,C16H24N2PbI4,\"(MBA)2PbI4, Œ±-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",bismethylbenzylaminium lead (II) iodide,2,single crystal,,,,,,,,\"PbO, (R/S)-MBA ((R/S)-methylbenzylamine / (R/S)-1-phenylethylamine), HI\",Orange plate-like crystals,\"PbO and R- or S-C6H5C2H4NH2 were added to HI. The solution fully dissolved after refluxing at 100 degrees Celsius for 3 hours. It was then cooled slowly over four days, over which time orange crystals began precipitating below 60 degrees.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer was used with monocrhomated Mo Kalpha radiation. Omega-scans of width 0.3 degrees were used to collect the data, and data reduction was performed with the SAINT+ program, version 6.02. Face indexed absorption corrections were performed with the XPREP program. The crystal structure was solved at -100 degrees Celsius using the SHELXS-97 program.\"\r\n10.1039/B618196A,Bis(cyclopropylammonium) lead iodide,(C3H5NH3)2PbI4,\"Cyclopropylammonium lead iodide, bis(cyclopropylaminium) tetraiodoplumbate(II)\",C3NH8,\"PbI4, Lead iodide\",bis(cyclopropylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, C3H5NH2\",Yellow crystals,\"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\"\r\n10.1039/B618196A,Bis(cyclobutylammonium) lead iodide,(C4H7NH3)2PbI4,\"Cyclobutylammonium lead iodide, bis(cyclobutylaminium) tetraiodoplumbate(II)\",C4H10N,\"PbI4, Lead iodide\",bis(cyclobutylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, C4H7NH2\",Orange crystals,\"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\"\r\n10.1039/B618196A,Bis(cyclopentylammonium) lead iodide,(C5H9NH3)2PbI4,\"Cyclopentylammonium lead iodide, bis(cyclopentylaminium) tetraiodoplumbate(II)\",C5NH12,\"PbI4, Lead iodide\",bis(cyclopentylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, C5H9NH2\",Orange crystals,\"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\"\r\n10.1039/B618196A,Bis(cyclohexylammonium) lead iodide,(C6H14N)2PbI4,\"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",C6H14N,\"PbI4, Lead iodide\",bis(cyclohexylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, C6H11NH2\",Orange crystals,\"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\"\r\n10.1039/B618196A,Tris(cycloheptylammonium) lead iodide,(C7H13NH3)3PbI4,\"Cycloheptylammonium lead iodide, tris(cycloheptylaminium) tetraiodoplumbate(II)\",C7H13NH3,\"PbI4, Lead iodide\",tris(cycloheptylaminium) lead (II) iodide,1,single crystal,,,,,,,,\"PbI2, HI, C7H13NH2\",Yellow crystals,\"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\"\r\n10.1039/B618196A,Cyclooctylammonium lead iodide,(C8H15NH3)PbI4,\"Cyclooctylammonium lead iodide, cyclooctylaminium tetraiodoplumbate(II)\",C8H15NH3,\"PbI4, Lead iodide\",cyclooctylaminium lead (II) iodide,1,single crystal,,,,,,,,\"PbI2, HI, C8H15NH2\",Yellow crystals,\"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\"\r\n10.1039/b805417g,bis(1-Dodecylammonium) lead iodide,C24H56N2PbI4,\"bis(dodecane-1-aminium) tetraiodoplumbate(II), (C12H25NH3)2PbI4\",C12H28N,\"PbI4, Lead iodide\",bis(dodecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI, C12H25NH2, methanol, ethyl acetate\",yellow plate-like crystal,0.048 g PbI2 (0.104 mmol) was added into 3 mL 47% HI. Then 0.030 g C12H25NH2 (0.162 mmol) was added into the above solution. The formed precipitation then dissolved into methanol (5 mL)–ethyl acetate (3 mL) mixture. The yellow single crystals were obtained by slow evaporation over a number of days.,Single crystal X-ray diffraction,\"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data.\r\nSAINT-NT16 was used to do data reduction and cell refinement.  XPREP16 was used to determine space groups.  WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\"\r\n10.1039/b805417g,bis(1-Dodecylammonium) lead iodide,C24H56N2PbI4,\"bis(dodecane-1-aminium) tetraiodoplumbate(II), (C12H25NH3)2PbI4\",C12H28N,\"PbI4, Lead iodide\",bis(dodecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI, C12H25NH2, methanol, ethyl acetate\",Orange plate-like crystal,0.048 g PbI2 (0.104 mmol) was added into 3 mL 47% HI. Then 0.030 g C12H25NH2 (0.162 mmol) was added into the above solution. The formed precipitation then dissolved into methanol (5 mL)–ethyl acetate (3 mL) mixture. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase-transition at higher temperature to obtain the orange monoclinic phase.,Single crystal X-ray diffraction,\"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data.\r\nSAINT-NT16 was used to do data reduction and cell refinement.  XPREP16 was used to determine space groups.  WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\"\r\n10.1039/b805417g,bis(1-tetradecylammonium) lead iodide,C28H64N2PbI4,\"bis(tetradecane-1-aminium) tetraiodoplumbate(II), (C14H29NH3)2PbI4\",C14H32N,\"PbI4, Lead iodide\",bis(tetradecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",yellow plate-like crystal,\"0.015 g PbI2 (0.104 mmol) was added  into 1 mL 47% HI. Then, 0.010 g C14H29NH2 (0.047 mmol) was added to the above solution. The formed precipitation was then dissolved into 5 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days.\",Single crystal X-ray diffraction,A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\r\n10.1039/b805417g,bis(1-tetradecylammonium) lead iodide,C28H64N2PbI4,\"bis(tetradecane-1-aminium) tetraiodoplumbate(II), (C14H29NH3)2PbI4\",C14H32N,\"PbI4, Lead iodide\",bis(tetradecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",Red plate-like crystal,\"0.015 g PbI2 (0.104 mmol) was added  into 1 mL 47% HI. Then, 0.010 g C14H29NH2 (0.047 mmol) was added to the above solution. The formed precipitation was then dissolved into 5 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase transition at a higher temperature to obtain the red monoclinic phase.\",Single crystal X-ray diffraction,A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\r\n10.1039/b805417g,bis(1-hexadecylammonium) lead iodide,C32H72N2PbI4,\"bis(hexadecane-1-aminium) tetraiodoplumbate(II), (C16H33NH3)2PbI4\",C16H36N,\"PbI4, Lead iodide\",bis(hexadecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",yellow plate-like crystal,\"0.062 g PbI2 (0.134 mmol) was added into 1 mL 47% HI. Then, 0.009 g C16H33NH2 (0.037 mmol) was added to the above solution. The formed precipitation was then dissolved into 8 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days.\",Single crystal X-ray diffraction,A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\r\n10.1039/b805417g,bis(1-hexadecylammonium) lead iodide,C32H72N2PbI4,\"bis(hexadecane-1-aminium) tetraiodoplumbate(II), (C16H33NH3)2PbI4\",C16H36N,\"PbI4, Lead iodide\",bis(hexadecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",Red plate-like crystal,\"0.062 g PbI2 (0.134 mmol) was added into 1 mL 47% HI. Then, 0.009 g C16H33NH2 (0.037 mmol) was added to the above solution. The formed precipitation was then dissolved into 8 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase transition at a higher temperature to obtain the red monoclinic phase.\",Single crystal X-ray diffraction,A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\r\n10.1039/b805417g,bis(1-octadecylammonium) lead iodide,C36H80N2PbI4,\"bis(octadecane-1-aminium) tetraiodoplumbate(II), (C18H37NH3)2[PbI4]\",C18H40N,\"PbI4, Lead iodide\",bis(octadecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",yellow plate-like crystal,\"0.033g PbI2 (0.072 mmol) was added  into 1 mL 47% HI. Then, 0.008 g C18H37NH2 (0.030 mmol) was added to the above solution. The formed precipitation was then dissolved into 15 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days.\",Single crystal X-ray diffraction,A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\r\n10.1039/b805417g,bis(1-octadecylammonium) lead iodide,C36H80N2PbI4,\"bis(octadecane-1-aminium) tetraiodoplumbate(II), (C18H37NH3)2[PbI4]\",C18H40N,\"PbI4, Lead iodide\",bis(octadecane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",orange-reddish plate-like crystal,\"0.033g PbI2 (0.072 mmol) was added into 1 mL 47% HI. Then, 0.008 g C18H37NH2 (0.030 mmol) was added to the above solution. The formed precipitation was then dissolved into 15 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase transition at a higher temperature to obtain the orange-red monoclinic phase.\",Single crystal X-ray diffraction,A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (λ = 0.71073 Å) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\r\n10.1039/B819455F,Bis(cyclopropylammonium) lead bromide,(C3H5NH3)2PbBr4,\"Cyclopropylammonium lead bromide, bis(cyclopropylaminium) tetrabromoplumbate(II)\",C3H5NH3,\"PbBr4, Lead bromide\",bis(cyclopropylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"PbBr2, HBr, C3H5NH2\",Colorless crystals,\"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Bis(cyclobutylammonium) lead bromide,(C4H7NH3)2PbBr4,\"Cyclobutylammonium lead bromide, bis(cyclobutylaminium) tetrabromoplumbate(II)\",C4H7NH3,\"PbBr4, Lead bromide\",bis(cyclobutylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"PbBr2, HBr, C4H7NH2\",Colorless crystals,\"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Bis(cyclopentylammonium) lead bromide,(C5H9NH3)2PbBr4,\"Cyclopentylammonium lead bromide, bis(cyclopentylaminium) tetrabromoplumbate(II)\",C5H9NH3,\"PbBr4, Lead bromide\",bis(cyclopentylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"PbBr2, HBr, C5H9NH2\",Colorless crystals,\"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Bis(cyclohexylammonium) lead bromide,(C6H14N)2PbBr4,\"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",C6H14N,\"PbBr4, Lead bromide\",bis(cyclohexylaminium) lead (II) bromide,2,single crystal,,,,,,,,\"PbBr2, HBr, C6H11NH2\",Orange crystals,\"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Tris(cycloheptylammonium) lead bromide,(C7H13NH3)3PbBr4,\"Cycloheptylammonium lead bromide, tris(cycloheptylaminium) tetrabromoplumbate(II)\",C7H13NH3,\"PbBr4, Lead bromide\",tris(cycloheptylaminium) lead (II) bromide,1,single crystal,,,,,,,,\"PbBr2, HBr, C7H13NH2\",Colorless crystals,\"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Cyclooctylammonium lead bromide,(C8H15NH3)PbBr4,Cyclooctylammonium tetrabromoplumbate(II),C8H15NH3,\"PbBr4, Lead bromide\",cyclooctylaminium lead (II) bromide,1,single crystal,,,,,,,,\"PbBr2, HBr, C8H15NH2\",Colorless crystals,\"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Bis(cyclopropylammonium) lead chloride,(C3H5NH3)2PbCl4,\"Cyclopropylammonium lead chloride, bis(cyclopropylaminium) tetrachloroplumbate(II)\",C3H5NH3,\"PbCl4, Lead chloride\",bis(cyclopropylaminium) lead (II) chloride,2,single crystal,,,,,,,,\"PbCl2, HCl, C3H5NH2\",Colorless crystals,\"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Bis(cyclobutylammonium) lead chloride,(C4H7NH3)2PbCl4,\"Cyclobutylammonium lead chloride, bis(cyclobutylaminium) tetrachloroplumbate(II)\",C4H7NH3,\"PbCl4, Lead chloride\",bis(cyclobutylaminium) lead (II) chloride,2,single crystal,,,,,,,,\"PbCl2, HCl, C4H7NH2\",Colorless crystals,\"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Bis(cyclopentylammonium) lead chloride,(C5H9NH3)2PbCl4,\"Cyclopentylammonium lead chloride, bis(cyclopentylaminium) tetrachloroplumbate(II)\",C5H9NH3,\"PbCl4, Lead chloride\",bis(cyclopentylaminium) lead (II) chloride,2,single crystal,,,,,,,,\"PbCl2, HCl, C5H9NH2\",Colorless crystals,\"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Bis(cyclohexylammonium) lead chloride,(C6H11NH3)2PbCl4,\"Cyclohexylammonium lead chloride, bis(cyclohexylaminium) tetrachloroplumbate(II)\",C6H11NH3,\"PbCl4, Lead chloride\",bis(cyclohexylaminium) lead (II) chloride,2,single crystal,,,,,,,,\"PbCl2, HCl, C6H11NH2\",Colorless crystals,\"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Tris(cycloheptylammonium) lead chloride,(C7H13NH3)3PbCl4,\"Cycloheptylammonium lead chloride, tris(cycloheptylaminium) tetrachloroplumbate(II)\",C7H13NH3,\"PbCl4, Lead chloride\",tris(cycloheptylaminium) lead (II) chloride,1,single crystal,,,,,,,,\"PbCl2, HCl, C7H13NH2\",Colorless crystals,\"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B819455F,Cyclooctylammonium lead chloride,(C8H15NH3)PbCl4,Cyclooctylammonium tetrachloroplumbate(II),C8H15NH3,\"PbCl4, Lead chloride\",cyclooctylaminium lead (II) chloride,2,single crystal,,,,,,,,\"PbCl2, HCl, C8H15NH2\",Colorless crystals,\"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",Single-crystal X-ray diffraction,\"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\"\r\n10.1039/B917824D,Bis(3-propanolammonium) lead iodide,C6H20N2O2PbI4,\"(HO(CH2)3NH3)2PbI4, bis(3-propanolaminium) tetraiodoplumbate(II)\",C3H10NO,\"PbI4, Lead iodide\",bis(3-propanolaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI(47%), propanolamine (HOC3H6NH2)\",Red crystals,PbI2 (0.495 mmol; 0.228 gm) was dissolved in 1 mL HI solution. Then HOC3H6NH2 (1.70 mmol; 0.128 g) was added and was dissolved by refluxing the solution for one hour at 90 degrees Celsius. Red crystals were then grown by cooling the solution at 2 degrees per hour to -7 degrees.,Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,Bis(2-iodoethylammonium) lead iodide,C4H14N2PbI6,\"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",C2H7NI,\"PbI4, Lead iodide\",bis(2-iodoethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI(47%), ethanol amine (HOC2H4NH2)\",Yellow crystals,\"PbI2 (0.434 mmol; 0.2 g) was dissolved in 2 mL HI solution. Then HOC2H4NH2 (0.798 mmol; 0.036 g) was added and was dissolved by refluxing for 12 hours. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled at 2 degrees Celsius per hour to room temperature, causing yellow crystals to precipitate.\",Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,Bis(3-iodopropylammonium) lead iodide,C6H18N2PbI6,\"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",C3H9NI,\"PbI4, Lead iodide\",bis(3-iodopropylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI(47%), propanolamine (HOC3H6NH2)\",Yellow crystals,\"PbI2 (0.610 mmol; 0.281 g) was dissolved in 1.5 mL HI solution. Then HOC3H6NH2 (0.945 mmol; 0.071 g) was added and was dissolved by refluxing for 2 hours at 90 degrees Celsius. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled at 2 degrees Celsius per hour to room temperature, causing yellow crystals to precipitate.\",Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,Bis(4-iodobutylammonium) lead iodide,C8H22N2PbI6,\"(I(CH2)4NH3)2PbI4, bis(4-iodobutylaminium) tetraiodoplumbate(II)\",C4H11NI,\"PbI4, Lead iodide\",bis(4-iodobutylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI(47%), butanolamine (HOC4H8NH2), ethyl acetate\",Yellow crystals,PbI2 (0.178 mmol; 0.082 g) was dissolved in 1 mL HI solution. Then HOC4H8NH2 (0.449 mmol; 0.040 g) was added. The precipitate was dissolved at 3 mL ethyl acetate and was kept undisturbed at room temperature. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom.,Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,Bis(5-iodopentylammonium) lead iodide,C10H26N2PbI6,\"(I(CH2)5NH3)2PbI4, bis(5-iodopentylaminium) tetraiodoplumbate(II)\",C5H13NI,\"PbI4, Lead iodide\",bis(5-iodopentylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI(47%), pentanolamine (HOC5H10NH2)\",Orange crystals,\"PbI2 (0.325 mmol; 0.236 g) was dissolved in 2 mL HI solution. Then HOC5H10NH2 (1.26 mmol; 0.130 g) was added. The precipitate was dissolved at room temperature via ultrasound. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled in a fridge to 5 degrees Celsius, causing orange crystals to precipitate.\",Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,Bis(6-iodohexylammonium) lead iodide,C12H30N2PbI6,\"(I(CH2)6NH3)2PbI4, bis(6-iodohexylaminium) tetraiodoplumbate(II)\",C6H15NI,\"PbI4, Lead iodide\",bis(6-iodohexylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI (47%), hexanolamine (HOC6H12NH2)\",Orange crystals,\"PbI2 (0.434 mmol; 0.200 g) was dissolved in 2 mL HI solution. Then HOC6H12NH2 (0.922 mmol; 0.108 g) was added. The precipitate was dissolved at room temperature via ultrasound. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled in a fridge to 5 degrees Celsius, causing orange crystals to precipitate.\",Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,Bis(2-bromoethylammonium) lead iodide,C4H14N2Br2PbI4,\"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",C2H7NBr,\"PbI4, Lead iodide\",bis(2-bromoethylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI, BrC2H4NH2·HBr\",Red crystals,\"PbI2 (0.113 mmol; 0.052 g)  was dissolved in 2 mL HI solution. Then BrC2H4NH2·HBr (0.376 mmol; 0.077 g) was added. The precipitate was dissolved at room temperature via ultrasound. The solution was then cooled in a fridge to 5 degrees Celsius, causing red crystals to precipitate.\",Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,\"2,2′-dithiodiethanammonium lead iodide\",C4H14N2S2PbI4,\"(NH3(CH2)2S-S(CH2)2NH3)PbI4, 2,2‚Ä≤-dithiodiethanaminium tetraiodoplumbate(II)\",C2H7NS,\"PbI4, Lead iodide\",\"2,2′-dithiodiethanaminium lead (II) iodide\",2,single crystal,,,,,,,,\"PbI2, HI (47%), HSC2H4NH2·HCl\",Orange crystals,\"PbI2 (0.252 mmol; 0.116 g) was dissolved in 4 mL HI solution. Then HSC2H4NH2·HCl (0.880 mmol; 0.1 g) was added and immediately formed a yellow solid. The solution was then heated 90 degrees Celsius, causing the solution to become clear after a few minutes. The solution was then cooled to room temperature at the rate of 2 degrees per hour, causing yellow and orange crystals to precipitate. The orange crystals were the perovskite compound and the yellow crystals were (NH3(CH2)2S-S(CH2)2NH3)2PbI5·I.\",Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,\"Iodo-bis(2,2′-dithiodiethanammonium) lead iodide\",C8H28N4S4PbI6,\"(NH3(CH2)2S-S(CH2)2NH3)2PbI5¬∑I, iodo-bis(2,2‚Ä≤-dithiodiethanaminium) pentaiodoplumbate(II)\",C4H14N2S2I,\"PbI4, Lead iodide\",\"iodo-bis(2,2′-dithiodiethanaminium) lead (II) iodide\",1,single crystal,,,,,,,,\"PbI2, HI (47%), HSC2H4NH2·HCl\",Yellow crystals,\"PbI2 (0.252 mmol; 0.116 g) was dissolved in 4 mL HI solution. Then HSC2H4NH2·HCl (0.880 mmol; 0.1 g) was added and immediately formed a yellow solid. The solution was then heated 90 degrees Celsius, causing the solution to become clear after a few minutes. The solution was then cooled to room temperature at the rate of 2 degrees per hour, causing yellow and orange crystals to precipitate. The yellow crystals were used for the experiment.\",Single-crystal X-ray diffraction,A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\r\n10.1039/B917824D,Bis(ethanolammonium) lead iodide,C4H16N2O2PbI4,\"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",OC2NH8,\"PbI4, Lead iodide\",,2,single crystal,,,,,,,,\"PbI2, HI, EOA, diethyl ether\",Red single crystals (EOA2PbI4),\"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 μL, 1.3 mmol) is added. This solution is sonicated at room temperature  for five minutes. It is then kept at 3 °C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",Single-crystal X-ray diffraction,\"Single crystal X-ray diffraction data was collected at 173 K using a Bruker SMART 1K CCD detectordiffractometer with graphite monochromated Mo Kα radiation (λ = 0.71073 Å). Software used in this process was Bruker SAINT+ and SHELXS-97. Further data was gathered using PLATON, WinGx, ORTEP, and DIAMOND.\"\r\n10.1039/c0dt01805h,Bis(nonylammonium) lead ioide,C18H44N2PbI4,\"bis(Nonylammonium)tetraiodoplumbate(II), (C9H19NH3)2PbI4\",C9H22N,\"PbI4, Lead iodide\",bis(nonane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, HI (47% in water), C9H19NH2\",Orange plate-like crystal,0.024 g PbI2 (0.052 mmol) was dissolved in 7 ml HI. 0.015 g C9H19NH2 (0.105 mmol) was added to it. The formed precipitate was dissolved by refluxing for 2 h at 90 degrees C. The solution was slowly cooled at 2 degrees C/hr to room temperature.,Single Crystal X-ray diffraction,Bruker Apex II CCD diffractometer11 with graphite-monochromated Mo-Kα1 radiation (λ = 0.71073 Å)\r\n10.1039/c3ee43822h,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"Methylamine (CH3NH2), (HI) 57 wt % in water, PbI2\",MAPbI3 film,React ~24 mL methylamine (CH3NH2) solution 33 wt% in absolute ethanol with ~10 mL hydroiodic acid (HI) 57 wt % in water with excess methylamine under nitrogen atmosphere in ~100 mL ethanol at room temperature. Crystallize methylammonium iodide (CH3NH3I) using a rotary evaporator to form a white colored powder. Prepare MAPbI3 precursor by dissolving equimolar amounts of methylammonium iodide and PbI2 in DMF at 0.88M in a nitrogen-filled glovebox. Spin-coat film at 2000rpm and anneal at 100 °C for 5 minutes in the glovebox.,Optical absorption,Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere. Estimated band gap was determined from the extrapolation of the linear region to the energy-axis intercept in the direct bandgap Tauc plot.\r\n10.1039/c3ee43822h,Cesium lead iodide,CsPbI3,\"cesium lead iodide, cesium triiodoplumbate(II)\",None,CsPbI3,cesium lead(II) iodide,3,film,,,,,,,,\"CsI, PbI2, dimethyl sulfoxide\",CsPbI3 film,\"Equimolar amounts of CsI and PbI2 were dissolved in dimethyl sulfoxide at 0.6M, in a nitrogen-filled glovebox. Films were spin-coated at 2000rpm and annealed at 100 degrees C for 5 minutes in the glovebox.\",Optical absorption,\"Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\r\nEstimated band gap was determined from the extrapolation of the linear region to the energy-axis intercept in the direct bandgap Tauc plot.\"\r\n10.1039/c3ee43822h,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,film,,,,,,,,\"FAI, PbI2, N,N-dimethylformamide (DMF)\",FAPbI3 film,\"FAI and PbI2 were dissolved in anhydrous DMF in a 1:1 molar ratio, at 0.88M. 60µl of hydroiodic acid (57%w/w) was added to 1ml of the solution. The FAPbI3 precursor was diluted down to 0.55M with DMF. The precursor solution was spin-coated and annealed on glass in a nitrogen-filled glovebox at 170°C for 25 minutes.\",optical absorption,Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere. Estimated band gap was determined from the extrapolation of the linear region to the energy-axis intercept in the direct bandgap Tauc plot.\r\n10.1039/c3ee43822h,Cesium lead iodide,CsPbI3,\"cesium lead iodide, cesium triiodoplumbate(II)\",None,CsPbI3,cesium lead(II) iodide,3,film,,,,,,,,\"CsI, PbI2, dimethyl sulfoxide\",CsPbI3 film,\"Equimolar amounts of CsI and PbI2 were dissolved in dimethyl sulfoxide at 0.6M, in a nitrogen-filled glovebox. Films were spin-coated at 2000rpm and annealed at 100 degrees C for 5 minutes in the glovebox.\",Optical absorption,Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\r\n10.1039/c3ee43822h,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"Methylamine (CH3NH2), (HI) 57 wt % in water, PbI2\",MAPbI3 film,React ~24 mL methylamine (CH3NH2) solution 33 wt% in absolute ethanol with ~10 mL hydroiodic acid (HI) 57 wt % in water with excess methylamine under nitrogen atmosphere in ~100 mL ethanol at room temperature. Crystallize methylammonium iodide (CH3NH3I) using a rotary evaporator to form a white colored powder. Prepare MAPbI3 precursor by dissolving equimolar amounts of methylammonium iodide and PbI2 in DMF at 0.88M in a nitrogen-filled glovebox. Spin-coat film at 2000rpm and anneal at 100 °C for 5 minutes in the glovebox.,Optical absorption,Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\r\n10.1039/c3ee43822h,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,film,,,,,,,,\"FAI, PbI2, N,N-dimethylformamide (DMF)\",FAPbI3 film,\"FAI and PbI2 were dissolved in anhydrous DMF in a 1:1 molar ratio, at 0.88M. 60µl of hydroiodic acid (57%w/w) was added to 1ml of the solution. The FAPbI3 precursor was diluted down to 0.55M with DMF. The precursor solution was spin-coated and annealed on glass in a nitrogen-filled glovebox at 170°C for 25 minutes.\",optical absorption,Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 Polycrystals,\"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 °C to 46 °C over 6 hours and dry (100 °C/10 hours). Maintain solution temperature above 40 °C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 °C.\",Diffuse-reflectance UV-Vis absorption,Absorption optical gap is 1.51 eV using diffuse reflectance UV-Vis spectra calculated using the optical absorption coefficient (\\alpha) according to the Kubelka-Munk equation. Refer to Page 5637 Figure 11.\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 Polycrystals,\"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 °C to 46 °C over 6 hours and dry (100 °C/10 hours). Maintain solution temperature above 40 °C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 °C.\",Powder X-ray diffraction,\"Tetragonal/cubic phase transition was investigated using variable temperature powder X-ray diffraction. In situ XRD data were collected in asymmetric reflection mode under a static helium atmosphere on an INEL Equinox 3000 (Inel, Artenay, France) equipped with an XRK-900 reactor chamber (Anton-Paar, Graz, Austria), a curved position sensitive detector (Ine, Artenay, France), a copper Ka source and a Ge-(111) focusing mirror. Refer to Page 5636 Table 4.\"\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 polycrystals,\"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 °C to 46 °C over 6 hours and dry (100 °C/10 hours). Maintain solution temperature above 40 °C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 °C.\",Powder X-ray diffraction,\"Tetragonal/cubic phase transition was investigated using variable temperature powder X-ray diffraction. In situ XRD data were collected in asymmetric reflection mode under a static helium atmosphere on an INEL Equinox 3000 (Inel, Artenay, France) equipped with an XRK-900 reactor chamber (Anton-Paar, Graz, Austria), a curved position sensitive detector (Ine, Artenay, France), a copper Ka source and a Ge-(111) focusing mirror. Refer to Page 5636 Table 4.\"\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",Black MAPbI3 crystals,\"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 °C for 2 h with constant stirring. Evaporate at 50 °C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 °C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 °C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 °C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",Single crystal X-ray diffraction,A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution-grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5° 2theta. Refer to Page 5637 Table 8.\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",Black MAPbI3 crystals,\"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 °C for 2 h with constant stirring. Evaporate at 50 °C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 °C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 °C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 °C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",Single crystal X-ray diffraction,A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5° 2theta. Refer to Page 5637 Table 8.\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",Black MAPbI3 crystals,\"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 °C for 2 h with constant stirring. Evaporate at 50 °C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 °C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 °C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 °C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",Single crystal X-ray diffraction,\"A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5° 2theta. Refined. Refer to Page 5636 Table 6, 7.\"\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,CASTEP 50,DFT,PBE-GGA,4x4x4,,,,,,,,\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,CASTEP 50,DFT,PBE-GGA,4x4x4,,,,,,,,\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,CASTEP 50,DFT,PBE-GGA,4x4x4,,,,,,,,\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,CASTEP 50,DFT,PBE-GGA,4x4x4,,,,,,,,\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 Polycrystals,\"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 °C to 46 °C over 6 hours and dry (100 °C/10 hours). Maintain solution temperature above 40 °C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 °C.\",Powder X-ray diffraction,\"Tetragonal/cubic phase transition was investigated using variable temperature powder X-ray diffraction. In situ XRD data were collected in asymmetric reflection mode under a static helium atmosphere on an INEL Equinox 3000 (Inel, Artenay, France) equipped with an XRK-900 reactor chamber (Anton-Paar, Graz, Austria), a curved position sensitive detector (Ine, Artenay, France), a copper Ka source and a Ge-(111) focussing mirror.\r\n\r\nTwo different heating experiments were conducted. In the first, MAPbI3 was heated to 85 °C in five degree steps starting from 25 °C, with data collected for 5 minutes at each holding temperature. The second experiment employed a continuous heating ramp at a rate of 1° min^-1 during which 30 measurements of 120 seconds were performed. Each measurement corresponds to a temperature span of 2 °C; the final temperature of each measurement was recorded in the measurement file. Five empty sample holder measurements were conducted at room temperature in order to establish the chamber background.\r\n\r\nRefer to Page 5633 Results and discussion; Page 5634 Figure 4 and Figure 5.\"\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 Polycrystals,\"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 °C to 46 °C over 6 hours and dry (100 °C/10 hours). Maintain solution temperature above 40 °C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 °C.\",Differential scanning calorimetry,Differential scanning calorimetry (DSC) was conducted on a Q10 V9.9 Build 303 calorimeter (TA Instruments) at a rate of 5 °C min^-1 over a temperature range from 25 °C to 200 °C under nitrogen. Page 5633 Results and discussion; Page 5635 Figure 6 and Figure 7.\r\n10.1039/c3ta10518k,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",Black MAPbI3 Single crystals,\"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 °C for 2 h with constant stirring. Evaporate at 50 °C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 °C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 °C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 °C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",Single crystal X-ray diffraction,A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5 ° 2\\theta. Refer to Page 5637 Figure 11.\r\n10.1039/c4cc09944c,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead acetate, HI (aq., 57 wt%), CH3NH2 (aq., 40%)\",Yellow MAPbI3 thin film (10 nm grain size),\"Dissolve 2.5 g of lead acetate (Sigma) in 10 mL hydroiodic acid (aq., 57 wt%, Sigma) in a 50 mL round bottom flask and heat to 100 °C in an oil bath. \r\n\r\nAdd 0.597 g of CH3NH2 (aq., 40%, Sigma) dropwise to a further 2 mL of hydroiodic acid kept at 0 °C in an ice bath under stirring. \r\n\r\nAdd the methylammonium iodide solution to the lead acetate solution and cool over two hours to 46 °C, affording a black precipitate.\r\n\r\nFilter and dry the black precipitate for 12 h at 100 °C. Average yield was 3.1 g, 75.2%. Repeat until 8 g of product has been obtained.\",Powder neutron diffraction,\"Data were collected using the D20 instrument at the ILL Grenoble operating in high take-off angle, higher resolution mode. 8 g of finely ground MAPbI3 was placed in a 7 mm diameter vanadium can. Data were collected for 90 minutes at 100 K. Raw diffraction data were corrected against detector efficiency and analysed using the GSAS/EXPGUI program suite; structure refinements for the long data collections at 100, 180 and 350 K were undertaken as described in the ESI. Refer to a,b,c, space group from ESI Table S1.1, volume from Garnett PRL, Structure Refinement from ESI.\"\r\n10.1039/c4cc09944c,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead acetate, HI (aq., 57 wt%), CH3NH2 (aq., 40%)\",Yellow MAPbI3 thin film (10 nm grain size),\"Dissolve 2.5 g of lead acetate (Sigma) in 10 mL hydroiodic acid (aq., 57 wt%, Sigma) in a 50 mL round bottom flask and heat to 100 °C in an oil bath. \r\n\r\nAdd 0.597 g of CH3NH2 (aq., 40%, Sigma) dropwise to a further 2 mL of hydroiodic acid kept at 0 °C in an ice bath under stirring. \r\n\r\nAdd the methylammonium iodide solution to the lead acetate solution and cool over two hours to 46 °C, affording a black precipitate.\r\n\r\nFilter and dry the black precipitate for 12 h at 100 °C. Average yield was 3.1 g, 75.2%. Repeat until 8 g of product has been obtained.\",Powder neutron diffraction,\"Data were collected using the D20 instrument at the ILL Grenoble operating in high take-off angle, higher resolution mode. 8 g of finely ground MAPbI3 was placed in a 7 mm diameter vanadium can. Data were collected for 90 minutes at 352 K. Raw diffraction data were corrected against detector efficiency and analysed using the GSAS/EXPGUI program suite; structure refinements for the long data collections at 100, 180 and 350 K were undertaken as described in the ESI. Refer to ESI Table S3.1.\"\r\n10.1039/c4cc09944c,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead acetate, HI (aq., 57 wt%), CH3NH2 (aq., 40%)\",Yellow MAPbI3 thin film (10 nm grain size),\"Dissolve 2.5 g of lead acetate (Sigma) in 10 mL hydroiodic acid (aq., 57 wt%, Sigma) in a 50 mL round bottom flask and heat to 100 °C in an oil bath. \r\n\r\nAdd 0.597 g of CH3NH2 (aq., 40%, Sigma) dropwise to a further 2 mL of hydroiodic acid kept at 0 °C in an ice bath under stirring. \r\n\r\nAdd the methylammonium iodide solution to the lead acetate solution and cool over two hours to 46 °C, affording a black precipitate.\r\n\r\nFilter and dry the black precipitate for 12 h at 100 °C. Average yield was 3.1 g, 75.2%. Repeat until 8 g of product has been obtained.\",Powder neutron diffraction,\"Data were collected using the D20 instrument at the ILL Grenoble operating in high take-off angle, higher resolution mode. 8 g of finely ground MAPbI3 was placed in a 7 mm diameter vanadium can. Data were collected for 90 minutes at 180 K. Raw diffraction data were corrected against detector efficiency and analysed using the GSAS/EXPGUI program suite; structure refinements for the long data collections at 100, 180 and 350 K were undertaken as described in the ESI. Refer to ESI Table S2.1.\"\r\n10.1039/C5CP02605A,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",MAPbI3 film,\"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 °C for 2 h. Evaporate solvents at 50 °C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 °C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 °C.\",Photoluminescence,Steady-state and time-resolved PL spectra were measured using an Edinburgh FLS920 spectroscopy system using laser excitation at 405 nm. PL peak is due to near-band edge transition. [Results and discussion paragraph 3; Fig. 2(b) Peak_OI]\r\n10.1039/C5CP02605A,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",MAPbI3 film,\"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 °C for 2 h. Evaporate solvents at 50 °C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 °C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 °C.\",Photoluminescence,Steady-state and time-resolved PL spectra were measured using an Edinburgh FLS920 spectroscopy system using laser excitation at 405 nm. PL peak is due to the near-band-edge transition. Refer to Results and discussion paragraph 2; Fig. 2(a) Peak_T.\r\n10.1039/C5CP02605A,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",MAPbI3 film,\"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 °C for 2 h. Evaporate solvents at 50 °C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 °C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2: NH4OH: H2O = 1: 1: 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 °C.\",Powder X-ray diffraction,The MAPbI3 film was characterized by X-ray diffraction (XRD) on a PANalytical X-ray diffractometer (Model EMPYREAN) with a monochromatic Cu Ka1 radiation. The lattice parameters were precisely determined using Si powders as the internal standard reference material. Refer to ESI Table SI.\r\n10.1039/C5CP02605A,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",MAPbI3 film,\"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 °C for 2 h. Evaporate solvents at 50 °C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 °C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 °C.\",Powder X-ray diffraction,The MAPbI3 film was characterized by X-ray diffraction (XRD) on a PANalytical X-ray diffractometer (Model EMPYREAN) with a monochromatic Cu Ka1 radiation. The lattice parameters were precisely determined using Si powders as the internal standard reference material. Refer to ESI Table SI.\r\n10.1039/C5CP02605A,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,,,,Laser excitation,\"Steady-state and time-resolved PL spectra were measured using an Edinburgh FLS920 spectroscopy system using laser excitation at 405 nm. PL peak is due to NBE emission, i.e., free exciton recombination due to the large binding energy at low temperature range.\"\r\n10.1039/C5CP02605A,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,\"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",MAPbI3 film,\"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 °C for 2 h. Evaporate solvents at 50 °C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 °C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 °C.\",Powder X-ray diffraction,No experimental details. Coexistence of the two phases at T from 150 to 130 K.\r\n10.1039/C5RA21291J,Methylammonium tin bromide,CH6NSnBr3,\"Methanaminium tribromostannate(II), MASnBr3, (CH3NH3)SnBr3\",CH6N,\"SnBr3, Tin bromide\",methanaminium tin bromide,3,film,,,,,,,,\"SnBr2 (tin(ii) bromide, 99.4%, Alfa Aesar), MABr (methylammonium bromide, CH3NH3Br, DYESOL), TiO2/FTO substrate\",400 nm thick MASnBr3 film,The film was fabricated by vapor deposition of SnBr2 and MABr at a ratio of 4 : 1 (0.4 Å s−1 : 0.1 Å s−1).,UV-vis absorption,The spectrum was measured using an Evolution 600 UV-Vis spectrophotometer.\r\n10.1039/c5sc01135c,\"Bis(3,4-dichlorobut-3-en-1-ammonium) lead bromide\",C8H20Cl4N2PbBr4,\"(BEA-Cl2)2[PbBr4], C8H20Br4Cl4N2Pb, bis(3,4-dichlorobut-3-en-1-aminium) tetrabromoplumbate(II)\",C4H10Cl2N,\"PbBr4, Lead bromide\",\"bis(3,4-dichlorobut-3-en-1-aminium) lead (II) bromide\",2,powder,,,,,,,,,,,,\r\n10.1039/c5sc01135c,\"Bis(3,4-dibromobut-3-en-1-ammonium) lead bromide\",C8H20Br4N2PbBr4,\"(BEA-Br2)2[PbBr4], C8H20Br8N2Pb, bis(3,4-dibromobut-3-en-1-aminium) tetrabromoplumbate(II)\",C4H10Br2N,\"PbBr4, Lead bromide\",\"bis(3,4-dibromobut-3-en-1-aminium) lead (II) bromide\",2,unknown,,,,,,,,,,,,\r\n10.1039/c5sc01135c,\"Bis(3,4-dibromobut-3-en-1-ammonium) lead chloride\",C8H20Br4N2PbCl4,\"(BEA-Br2)2[PbCl4], C8H20Br4N2PbCl4, bis(3,4-dibromobut-3-en-1-aminium) tetrachloroplumbate(II)\",C4H10Br2N,\"PbCl4, Lead chloride\",\"bis(3,4-dibromobut-3-en-1-aminium) lead (II) chloride\",2,single crystal,,,,,,,,,,,,\r\n10.1039/c5sc01135c,\"Bis(3,4-dibromobut-3-en-1-ammonium) lead bromide\",C8H20Br4N2PbBr4,\"(BEA-Br2)2[PbBr4], C8H20Br8N2Pb, bis(3,4-dibromobut-3-en-1-aminium) tetrabromoplumbate(II)\",C4H10Br2N,\"PbBr4, Lead bromide\",\"bis(3,4-dibromobut-3-en-1-aminium) lead (II) bromide\",2,single crystal,,,,,,,,\"(BEA)Cl (but-3-en-1-ammonium chloride), methanol, Cl¬2 (g), PbBr2, 9-M HBr\",Colorless plate-like crystals,\"First, a solution of (BEA)Cl (0.10 g, 0.93 mmol) in 10 mL of methanol was cooled to 0 º C, exposed to Cl2 gas for 2 minutes, and then allowed to stir for 1 hour in the dark. During this time, volatiles were removed under reduced pressure, and a colorless solid resulted. This solid was then dissolved in 3 mL of methanol and added to a stirred, 5-mL solution of PbBr2 (0.17 g, 0.46 mmol) in 9-M HBr at -10 ¬º C. After 10 minutes, a colorless precipitate was filtered through a glass frit and washed with diethyl ether at -10 º C. A colorless crystalline solid resulted and was held at reduced pressure for 1 hour to produce 0.303 g of product.\",Single-crystal X-Ray diffraction,The data were recorded using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo kα radiation. Data was corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\r\n10.1039/c5sc01135c,\"Bis(3,4-dichlorobut-3-en-1-ammonium) lead bromide\",C8H20Cl4N2PbBr4,\"(BEA-Cl2)2[PbBr4], C8H20Br4Cl4N2Pb, bis(3,4-dichlorobut-3-en-1-aminium) tetrabromoplumbate(II)\",C4H10Cl2N,\"PbBr4, Lead bromide\",\"bis(3,4-dichlorobut-3-en-1-aminium) lead (II) bromide\",2,single crystal,,,,,,,,\"(BEA)Cl (but-3-en-1-ammonium chloride), methanol, Cl¬2 (g), PbBr2, 9-M HBr\",Colorless plate-like crystals,\"First, a solution of (BEA)Cl (0.10 g, 0.93 mmol) in 10 mL of methanol was cooled to 0 º C, exposed to Cl2 gas for 2 minutes, and then allowed to stir for 1 hour in the dark. During this time, volatiles were removed under reduced pressure, and a colorless solid resulted. \r\nThis solid was then dissolved in 3 mL of methanol and added to a stirred, 5-mL solution of PbBr2 (0.17 g, 0.46 mmol) in 9-M HBr at -10 ¬º C. After 10 minutes, a colorless precipitate was filtered through a glass frit and washed with diethyl ether at -10 º C. A colorless crystalline solid resulted and was held at reduced pressure for 1 hour to produce 0.303 g of product.\",Single-crystal X-Ray diffraction,The data were recorded using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo kα radiation. Data was corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\r\n10.1039/c5sc01135c,\"Bis(3,4-dibromobut-3-en-1-ammonium) lead chloride\",C8H20Br4N2PbCl4,\"(BEA-Br2)2[PbCl4], C8H20Br4N2PbCl4, bis(3,4-dibromobut-3-en-1-aminium) tetrachloroplumbate(II)\",C4H10Br2N,\"PbCl4, Lead chloride\",\"bis(3,4-dibromobut-3-en-1-aminium) lead (II) chloride\",2,single crystal,,,,,,,,,,,Single-crystal X-Ray diffraction,The data were recorded using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo kα radiation. Data was corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\r\n10.1039/c5ta01125f,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HCl, CH3NH2 (40% soluble in water, Merck)\",\"MAPbCl3 single crystal ~1mm, colorless\",\"Precipitate polycrystalline MAPbCl3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 37 wt% HCl aqueous solution warmed (~90 °C) in a water bath. Then add an excess of HCl to prevent the co-precipitation of PbCl2 in agreement with previous work [2], along with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days. Refer to Page 9299 Section 2.1 Synthesis; Figure 2.\",UV-Vis absorption (diffuse reflectance),\"UV-Visible-NIR spectrophotometer (Shimadzu UV-3600) with integrating sphere attachment (ISR-3100) operating in the 300–1500 nm region. Highly refined barium sulfate powder (Wako, pure) was used as a reflectance standard. Optical absorption coefficient was determined according to the Kubelka–Munk equation. In this manner, optical band gaps for the perovskites were determined. Refer to Page 9300 Section 3.1 Paragraph 3; Figure 3,4.\"\r\n10.1039/c5ta01125f,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HBr, CH3NH2 (40% soluble in water, Merck)\",\"MAPbBr3 single crystal ~0.1mm, bright red/orange\",Precipitate polycrystalline MAPbBr3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 48 wt% HBr aqueous solution warmed (~90 °C) in a water bath. Then add another 2 ml of HBr solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days. Refer to Page 9299 Section 2.1 Synthesis; Figure 1.,UV-Vis absorption (diffuse reflectance),\"UV-Visible-NIR spectrophotometer (Shimadzu UV-3600) with integrating sphere attachment (ISR-3100) operating in the 300–1500 nm region. Highly refined barium sulfate powder (Wako, pure) was used as a reflectance standard. Optical absorption coefficient was determined according to the Kubelka–Munk equation. In this manner, optical band gaps for the perovskites were determined. Refer to Page 9300 Section 3.1 Paragraph 3; Figure 3,4.\"\r\n10.1039/c5ta01125f,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",MAPbI3 Single crystal,Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 °C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days. Refer to Page 9299 Section 2.1 Synthesis.,UV-Vis absorption (diffuse reflectance),\"UV-Visible-NIR spectrophotometer (Shimadzu UV-3600) with integrating sphere attachment (ISR-3100) operating in the 300–1500 nm region. Highly refined barium sulfate powder (Wako, pure) was used as a reflectance standard. Optical absorption coefficient was determined according to the Kubelka–Munk equation. In this manner, optical band gaps for the perovskites were determined. Refer to Page 9300 Section 3.1 Paragraph 3; Figure 3,4.\"\r\n10.1039/c5ta01125f,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HBr, CH3NH2 (40% soluble in water, Merck)\",\"MAPbBr3 single crystal ~0.1mm, bright red/orange\",Precipitate polycrystalline MAPbBr3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 48 wt% HBr aqueous solution warmed (~90 °C) in a water bath. Then add another 2 ml of HBr solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days. Refer to Page 9299 Section 2.1 Synthesis; Figure 1.,X-ray diffraction,Bruker D8 Advance diffractometer (Bragg–Brentano geometry) equipped with a Cu-Ka X-ray tube operated at 40 kV and 40 mA. Refer to Page 9300 Section 3.1 Paragraph 2.\r\n10.1039/c5ta01125f,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HCl, CH3NH2 (40% soluble in water, Merck)\",Colorless MAPbCl3 Single crystal ~1mm,\"Precipitate polycrystalline MAPbCl3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated aquous HCl solution (37 wt%) warmed (~90 °C) in a water bath. Then add an excess of HCl to prevent the co-precipitation of PbCl2 in agreement with previous work [2], along with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days.\",Powder X-ray diffraction,Bruker D8 Advance diffractometer (Bragg–Brentano geometry) equipped with a Cu-Ka X-ray tube operated at 40 kV and 40 mA. Refer to Page 9300 Section 3.1 Paragraph 2.\r\n10.1039/c5ta01125f,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 crystals,Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 °C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days.,Single crystal X-ray diffraction,\"Agilent Supernova diffractometer (Mo Kα, λ = 0.71073 Å) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibrate for at least one hour after the phase transition to obtain a higher quality dataset. Automated data processing and indexing procedures contained within the CrysAlisPro software. Refer to Page 9304 Section 3.4 Paragraph 2.\"\r\n10.1039/c5ta01125f,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 Single crystal,Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 °C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days.,X-ray diffraction,\"Agilent Supernova diffractometer (Mo Kα, λ = 0.71073 Å) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibriate for at least one hour after the phase transition to obtain a higher quality dataset. Manual indexing routine. Refer to Page 9304 Section 3.4 Paragraph 2; SI Table S3.\"\r\n10.1039/c5ta01125f,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 Single crystal,Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 °C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days.,X-ray diffraction,\"Agilent Supernova diffractometer (Mo Kα, λ = 0.71073 Å) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibrate for at least one hour after the phase transition to obtain a higher quality dataset. Manual indexing routine. Refer to Page 9304 Section 3.4 Paragraph 2; SI Table S5.\"\r\n10.1039/c5ta01125f,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",Black MAPbI3 Single crystal,Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 °C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 °C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 °C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 °C over 3 days.,X-ray diffraction,\"Agilent Supernova diffractometer (Mo Kα, λ = 0.71073 Å) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibrate for at least one hour after the phase transition to obtain a higher quality dataset. Manual indexing routine. Refer to Page 9304 Section 3.4 Paragraph 2; SI Table S5.\"\r\n10.1039/c6mh00053c,Bis(methylammonium) potassium bismuth chloride,C2H12N2KBiCl6,\"bis(methanaminium) potassium hexachlorobismuthate(II), (MA)2KBiCl6, methylammonium potassium bismuth chloride, (CH3NH3)2KBiCl6\",CH6N,\"KBiCl6, Potassium bismuth chloride\",bis(methanaminium) potassium bismuth chloride,3,single crystal,,,,,,,,\"methylammonium chloride (synthesized from methylamine solution (40 wt% in H2O) and HCl (37% in H2O)), HCl, BiCl3, K\",Colorless prismatic crystals,\"2.4 mmol CH3NH3Cl, 1.2 mmol KCl, and 1.2 mmol BiCl3 in 1 ml HCl acid solution were loaded in a stainless steel Parr autoclave. The hydrothermal reaction was performed at 423 K.\",Single crystal X-ray diffraction,\"Frames were collected in an Oxford Gemini E Ultra diffractometer with Mo Kα radiation (λ = 0.71073Å), equipped with an Eos CCD detector.\"\r\n10.1039/c6mh00053c,Bis(methylammonium) potassium bismuth chloride,CH6N+2KBiCl6,\"Bis(methanaminium) trichlorobismuthate(III) trichloropotassiate(I), (MA)2KBiCl6\",CH6N,KBiCl6,*,3,single crystal,,,,,,,,\"CH3NH3Cl (synthesized by reacting methylamine solution (40 wt% in H2O) and HCl (37% in H2O)), KCl, BiCl3\",crystalline powder,\"Hydrothermal synthesis at 423 K with 2.4 mmol CH3NH3Cl, 1.2 mmol KCl and 1.2 mmol BiCl3 in 1 ml HCl acid solution.\",Single crystal X-ray diffraction,\"Diffraction data were collected using Oxford Gemini E Ultra diffractometer, Mo Kα radiation (λ = 0.71073Å), equipped with an Eos CCD detector.\"\r\n10.1039/c6sc02848a,bis(6-Iodohexylammonium) lead iodide,C12H30N2I2PbI4,\"(IC6)2[PbI4], C12H30N2PbI6, bis(1-iodohexyl-6-aminium) tetraiodoplumbate(II)\",C6H15NI,\"PbI4, Lead iodide\",bis(1-iodohexyl-6-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"PbI2, 6-amino-1-hexanol, hydroiodic acid\",red-orange crystals,\"solid PbI2 (0.455 g, 0.987 mmol) and 6-amino-1-hexanol (0.272 g, 2.32 mmol) were dissolved in concentrated hydroiodic acid (2 mL). The solution was sonicated for 5 minutes and resulted in a yellow-orange solution. The colored solution was heated at 100º C for 3 hours and cooled to room temperature. This resulted in red-orange crystals that were filtered in glass frit and washed with diethyl ether.\",Single crystal X-ray diffraction,\"To determine the crystal structure, a crystal was coated in Paratone-N oil, mounted to a Mitegen loop/micromesh mount, and transferred to a Bruker D8 Venture diffractometer with Photon 100 CMOS detector.\"\r\n10.1039/c6sc02848a,bis(6-Iodohexylammonium) lead iodide,C12H30N2I2PbI4,\"(IC6)2[PbI4], C12H30N2PbI6, bis(1-iodohexyl-6-aminium) tetraiodoplumbate(II)\",C6H15NI,\"PbI4, Lead iodide\",bis(1-iodohexyl-6-aminium) lead (II) iodide,2,single crystal,VASP,DFT,\"Structure optimized with GGA + vdW, Electronic property with HSE+SOC\",4x4x1 (Monkhort-Pack),,PAW,,,,,,\r\n10.1039/c6sc02848a,bis(6-Iodohexylammonium) lead iodide,C12H30N2I2PbI4,\"(IC6)2[PbI4], C12H30N2PbI6, bis(1-iodohexyl-6-aminium) tetraiodoplumbate(II)\",C6H15NI,\"PbI4, Lead iodide\",bis(1-iodohexyl-6-aminium) lead (II) iodide,2,film,,,,,,,,\"PbI2, 6-amino-1-hexanol, hydroiodic acid, DMF\",230 - 270 nm thick film,\"solid PbI2 (0.455 g, 0.987 mmol) and 6-amino-1-hexanol (0.272 g, 2.32 mmol) were dissolved in concentrated hydroiodic acid (2 mL). The solution was sonicated for 5 minutes and resulted in a yellow-orange solution. The colored solution was heated at 100º C for 3 hours and cooled to room temperature. This resulted in red-orange crystals that were filtered in glass frit and washed with diethyl ether. The crystals were dissolved in DMF to prepare a 0.4 M solution. The solution was filtered through 0.22-μm pore size Teflon syringe filters. 50-100 μL of the solution was spun on quartz substrates at 3000 rpm for 50 s and then at 5000 rpm for 10 s. The films were annealed at 100 °C for 10 minutes.\",Uv-vis absorption,Data were recorded with an Agilent Cary 6000i spectrometer.\r\n10.1039/c6ta05055g,\"1,8-octyldiammonium lead iodide\",C8H22N2PbI4,\"OdAPbI4, [NH3(CH2)8NH3]PbI4, octane-1,8-diaminium tetraiodoplumbate(II)\",C8H22N2,\"PbI4, Lead iodide\",\"octane-1,8-diaminium lead (II) iodide\",2,single crystal,,,,,,,,\"1,8-diaminooctane (98%),  hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%)\",block-like crystals,\"1 mol 1,8-diaminooctane (98%) was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether .\r\n\r\nPbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to  −10 °C.\",Single crystal X-ray crystallography,\"Data were collected using a Bruker APEXII diffractometer (MoKα radiation), equipped with a CCD detector.\"\r\n10.1039/c6ta05055g,\"1,8-octyldiammonium lead iodide\",C8H22N2PbI4,\"OdAPbI4, [NH3(CH2)8NH3]PbI4, octane-1,8-diaminium tetraiodoplumbate(II)\",C8H22N2,\"PbI4, Lead iodide\",\"octane-1,8-diaminium lead (II) iodide\",2,film,,,,,,,,\"1,8-diaminooctane (98%), hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%), TiO2\",yellow film,\"1 mol 1,8-diaminooctane (98%) was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether . PbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to −10 °C.\r\n1:3.5 ratio of TiO2 Dyesol paste and ethanol (99.5%) produced a ∼250 nm mesoporous film on a microscopic slide. The film was sintered and was used as a substrate. DMF solution of the perovskite crystal was spin-coated and the film was heated at 90 °C for 10 min.\",UV-vis absorption,Spectra were recorded using UV-visible Cary 300 spectrophotometer.\r\n10.1039/c6ta05055g,\"1,6-diaminohexane lead iodide\",C6H18N2PbI4,\"HdAPbI4, hexane-1,6-diaminium tetraiodoplumbate(II)\",C6H18N2,\"PbI4, Lead iodide\",\"hexane-1,6-diaminium lead (II) iodide\",2,single crystal,,,,,,,,\"1,6-diaminohexane (98%), hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%)\",block-like crystals,\"1 mol 1,6-diaminohexane was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether. PbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to −10 °C.\",Single crystal X-ray crystallography,\"Data were collected using a Bruker APEXII diffractometer (MoKα radiation), equipped with a CCD detector.\"\r\n10.1039/c6ta05055g,\"1,6-diaminohexane lead iodide\",C6H18N2PbI4,\"HdAPbI4, hexane-1,6-diaminium tetraiodoplumbate(II)\",C6H18N2,\"PbI4, Lead iodide\",\"hexane-1,6-diaminium lead (II) iodide\",2,film,,,,,,,,\"1,6-diaminohexane (98%), hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%), TiO2\",yellow film,\"1 mol 1,6-diaminohexane (98%) was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether . PbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to −10 °C. 1:3.5 ratio of TiO2 Dyesol paste and ethanol (99.5%) produced a ∼250 nm mesoporous film on a microscopic slide. The film was sintered and was used as a substrate. DMF solution of the perovskite crystal was spin-coated and the film was heated at 90 °C for 10 min.\",UV-vis absorption,Spectra were recorded using UV-visible Cary 300 spectrophotometer.\r\n10.1039/c6ta05817e,Bis(methylammonium) thallium bismuth bromide,([CH3NH3]+)2TIBiBr6,\"Bis(methanaminium) tribromobismuthate(III) trichlorotantalate(I), (MA)2TIBiBr6\",CNH6,TIBiBr6,*,3,single crystal,,,,,,,,,,,,\r\n10.1039/c7cc02408h,Bis(phenethylammonium) cadmium iodide,C16H24N2CdI4,\"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",C8H12N,\"CdI4, Cadmium iodide\",bis(phenylethanaminium) cadmium iodide,0,single crystal,,,,,,,,\"methanol, CdI2 and 2-phenylethylammonium iodide\",,\"30 mL of methanol, 1.83 g of CdI2 and 2.49 g of 2-phenylethylammonium iodide (C6H5C2H4NH3I) was mixed together and stirred for 20 min. The 2-phenylethylammonium iodide was synthesized by mixing stoichiometric quantities of 2‐phenylethylamine and hydroiodic acid (57%). The final crystals were obtained by the slow evaporation of the solution.\",,\r\n10.1039/c7cc02408h,Bis(phenethylammonium) cadmium iodide,C16H24N2CdI4,\"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",C8H12N,\"CdI4, Cadmium iodide\",bis(phenylethanaminium) cadmium iodide,0,powder,,,,,,,,\"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",Colorless block-like crystals,\"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2‐phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",Powder X-ray diffraction,\r\n10.1039/c7cc02408h,Bis(phenethylammonium) cadmium iodide,C16H24N2CdI4,\"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",C8H12N,\"CdI4, Cadmium iodide\",bis(phenylethanaminium) cadmium iodide,0,single crystal,,,,,,,,\"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",Colorless block-like crystals,\"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2‐phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",Single crystal X-ray diffraction,Frames were collected using RAXIS IP diffractometer with Mo‐Kα radiation (λ = 0.71073 Å)\r\n10.1039/c7cc02408h,Bis(phenethylammonium) cadmium iodide,C16H24N2CdI4,\"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",C8H12N,\"CdI4, Cadmium iodide\",bis(phenylethanaminium) cadmium iodide,0,powder,,,,,,,,\"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",Colorless block-like crystals,\"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2‐phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",Powder X-ray diffraction,\r\n10.1039/c7cc02408h,Bis(phenethylammonium) cadmium iodide,C16H24N2CdI4,\"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",C8H12N,\"CdI4, Cadmium iodide\",bis(phenylethanaminium) cadmium iodide,0,powder,,,,,,,,\"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",Colorless block-like crystals,\"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2‐phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",,\r\n10.1039/c7cc02408h,Bis(phenethylammonium) cadmium iodide,C16H24N2CdI4,\"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",C8H12N,\"CdI4, Cadmium iodide\",bis(phenylethanaminium) cadmium iodide,0,powder,,,,,,,,\"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",Colorless block-like crystals,\"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2‐phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",,\r\n10.1039/c7cc02408h,Bis(phenethylammonium) cadmium iodide,C16H24N2CdI4,\"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",C8H12N,\"CdI4, Cadmium iodide\",bis(phenylethanaminium) cadmium iodide,0,powder,,,,,,,,\"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",Colorless block-like crystals,\"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2‐phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",Differential scanning calorimetry (DSC),\"A powder sample of crystals of (C6H5CH2CH2NH3)2(CdI4) was utilized in this experiment. DSC for heating and cooling was measured at a rate of change of 5 K/min. In the heating cycle, an anomaly occurred at 301 K, and in the cooling graph an anomaly arose at  297 K. A TA DSC Q2000 instrument was used to carry out the experiment.\"\r\n10.1039/c7sc01590a,\"2-methyl-1,5-pentanediamine lead bromide\",C6H18N2PbBr4,\"methyl-2-pentane-1,5-diaminium tetrabromoplumbate(II), (MPenDA)PbBr4, NH3C5H9CH3NH3PbBr4\",C6H18N2,\"PbBr4, Lead bromide\",\"methyl-2-pentane-1,5-diaminium lead(II) bromide\",2,single crystal,,,,,,,,\"2-methyl-1,5-pentanediamine, PbBr2,  HBr\",needle-like colorless crystal,\"0.34 mmol PbBr2, 0.35 mmol 2-methyl-1,5-pentanediamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo Kα radiation (λ=0.71073 Å).\r\n10.1039/c7sc01590a,Bis(butylammonium) lead bromide,C8H24N2PbBr4,\"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",C4H12N,\"PbBr4, Lead bromide\",bis(butyl-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"n-butylamine, PbBr2, HBr\",plate-like colorless crystals,\"0.34 mmol PbBr2, 0.7 mmol n-butylamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo Kα radiation (λ=0.71073 Å).\r\n10.1039/c7sc01590a,\"1,8-octyldiammonium lead bromide\",C8H22N2PbBr4,\"octane-1,8-diaminium tetrabromoplumbate(II), (ODA)PbBr4, NH3C8H16NH3PbBr4\",C8H22N2,\"PbBr4, Lead bromide\",\"octane-1,8-diaminium lead(II) bromide\",2,single crystal,,,,,,,,\"octanediamine, PbBr2, HBr\",plate-like colorless crystals,\"0.34 mmol PbBr2, 0.35 mmol octanediamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo Kα radiation (λ=0.71073 Å).\r\n10.1039/c7sc01590a,bis(4-aminobutonic acid) lead bromide,C8H20N2O4PbBr4,\"bis(4-aminobutanoic acid) tetrabromoplumbate(II), (GABA)2PbBr4, C8H20O4N2PbBr4, (C4H10NO2)2PbBr4\",C4H10NO2,\"PbBr4, Lead bromide\",bis(4-aminobutanoic acid) lead(II) bromide,2,single crystal,,,,,,,,\"3-carboxypropan-1-amine, PbBr2, HBr\",plate-like colorless crystals,\"0.34 mmol PbBr2, 0.7 mmol 3-carboxypropan-1-amine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo Kα radiation (λ=0.71073 Å).\r\n10.1039/c7sc01590a,3-(2-ammonioethyl)anilinium lead bromide,C8H14N2PbBr4,\"3-(2-ethanaminium)anilinium tetrabromoplumbate(II), (AEA)PbBr4\",C8H14N2,\"PbBr4, Lead bromide\",3-(2-ethanaminium)anilinium lead(II) bromide,2,single crystal,,,,,,,,\"3-(2-ammonioethyl)anilin, PbBr2, HBr\",plate-like colorless crystals,\"0.34 mmol PbBr2, 0.35 mmol 3-(2-ammonioethyl)anilin are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D85 diffractometer at the Advanced Light Source beamline 11.3.1 (λ=0.7749 Å).\r\n10.1039/c7sc01590a,\"1,4-butyldiammonium lead bromide\",C4H14N2PbBr4,\"butyl-1,4-diaminium tetrabromoplumbate(II), (BDA)PbBr4, C4N2H14PbBr4, NH3C4H8NH3PbBr4\",C4H14N2,\"PbBr4, Lead bromide\",\"butyl-1,4-diaminium lead(II) bromide\",2,single crystal,,,,,,,,\"butanediamine, PbBr2, HBr\",plate-like colorless crystals,\"0.34 mmol PbBr2, 0.35 mmol butanediamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo Kα radiation (λ=0.71073 Å).\r\n10.1039/c7sc01590a,Histammonium lead bromide,C5H11N3PbBr4,\"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",C5H11N3,\"PbBr4, Lead bromide\",4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide,2,single crystal,,,,,,,,\"Histamine, PbBr2, HBr\",plate-like yellow crystals,\"0.34 mmol PbBr2, 0.35 mmol histamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo Kα radiation (λ=0.71073 Å).\r\n10.1039/c7sc01590a,Histammonium lead bromide,C5H11N3PbBr4,\"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",C5H11N3,\"PbBr4, Lead bromide\",4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide,2,single crystal,,,,,,,,\"Histamine, PbBr2, HBr\",plate-like yellow crystals,\"0.34 mmol PbBr2, 0.35 mmol histamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 ˚C for 2 h to dissolve the solid, and then slowly cooled down to room temperature at −2 °C·hr−1.\",Single crystal X-ray diffraction,Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo Kα radiation (λ=0.71073 Å).\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,single crystal,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Single crystal X-ray diffraction,An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation was used to collect the single crystal XRD data.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,single crystal,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Single crystal X-ray diffraction,An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation was used to collect the single crystal XRD data.\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,single crystal,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Single crystal X-ray diffraction,An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation was used to collect the single crystal XRD data.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence excitation,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence excitation,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Photoluminescence excitation,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether.In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,single crystal,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Single crystal X-ray diffraction,An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation was used to collect the single crystal XRD data.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence excitation,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether.In an N2-filled glove box,  SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box,  SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence excitation,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,single crystal,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Single crystal X-ray diffraction,An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation was used to collect the single crystal XRD data.\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Photoluminescence excitation,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Photoluminescence,FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence quantum efficiency using integrating sphere,An integrating sphere incorporated in FLS980 spectrofluorometer (Edinburgh Instruments) was used to measure the PLQE.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Photoluminescence quantum efficiency using integrating sphere,An integrating sphere incorporated in FLS980 spectrofluorometer (Edinburgh Instruments) was used to measure the PLQE.\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Photoluminescence quantum efficiency using integrating sphere,An integrating sphere incorporated in FLS980 spectrofluorometer (Edinburgh Instruments) was used to measure the PLQE.\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Thermogravimetric analysis (TGA),\"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 °C/ min\u0002, under a nitrogen flux of 100 mL/min\u0002.\"\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium bromide) tin bromide\",C16H56N8Br4SnBr6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",C4H14N2Br,\"SnBr6, Tin bromide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",0,powder,,,,,,,,\"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",Colorless crystals,\"N,N′-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N′-dimethylethylene-1,2-diammonium bromide were mixed in a 1 : 4 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Thermogravimetric analysis (TGA),\"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 °C/ min\u0002, under a nitrogen flux of 100 mL/min\u0002.\"\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Thermogravimetric analysis (TGA),\"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 °C/ min\u0002, under a nitrogen flux of 100 mL/min\u0002.\"\r\n10.1039/C7SC04539E,\"tetra(N,N′-dimethylethylene-1,2-diammonium iodide) tin iodide\",C16H56N8I4SnI6,\"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",C4H14N2I,\"SnI6, Tin iodide\",\"tetra(N,N′-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",0,powder,,,,,,,,\"γ-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N′-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",Red crystals,\"N,N′-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N′-dimethylethylenediamine (1 equiv.) in ethanol at 0 °C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N′-dimethylethylene-1,2-diammonium iodide were mixed in a 1 : 4 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",Thermogravimetric analysis (TGA),\"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 °C/ min, under a nitrogen flux of 100 mL/min.\"\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Thermogravimetric analysis (TGA),\"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 °C/ min, under a nitrogen flux of 100 mL/min.\"\r\n10.1039/C7SC04539E,Bis(1-butyl-1-methylpyrrolidinium) antimony chloride,C18H40N2SbCl5,\"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",C9H20N,\"SbCl5, Antimony chloride\",bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride,0,powder,,,,,,,,\"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",Colorless crystals,Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.,Thermogravimetric analysis (TGA),\"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 °C/ min, under a nitrogen flux of 100 mL/min.\"\r\n10.1039/C7TA06679A,Tris(methylammonium) antimony iodide,C3H18N3Sb2I9,\"MA3Sb2I9, (CH3NH3)3Sb2I9, tris(methanaminium) nonaiodo diantimonate(III)\",CH6N,\"Sb2I9, Antimony iodide\",tris(methanaminium) antimony iodide,0,film,,,,,,,,\"SbI3 (99.998%), methylamine (CH3NH2, 40 wt.% in water), dimethylformamide (DMF), Aqueous hydroiodic acid (HI) (57 wt.% in water)\",orange MA2Sb2I9 film,SbI3 and MAI were dissolved in the DMF and heated at 70 °C overnight. The heating was stopped and a specific volume of HI was added to it. The solution was spin-coated (6000 rpm) onto ITO/PEDOT:PSS substrates and was annealed at 70 °C.,UV-vis absorption,The absorption spectrum was measured using a Jacobs V-670 UV–Vis spectrophotometer\r\n10.1039/c7tc04868h,N-(3-aminopropyl)imidazole lead chloride,C6H13N3PbCl4,\"N-(3-aminopropyl)imidazole tetrachloroplumbate(II),  3-(propane-1-aminium)imidazolium tetrachloroplumbate(II)\",C6H13N3,\"PbCl4, Lead chloride\",3-(propane-1-aminium)imidazolium lead (II) chloride,2,single crystal,,,,,,,,\"HCl (38%), methanol (99.5%), Pb(Ac)2.3H2O (99.5%), 1-(3-aminopropyl)imidazole (97%)\",colorless plate-like crystals,\"Step1: fabrication of 1-(3-Aminopropyl)imidazole chloride:\r\n1:1 mole ratio of 1-(3-aminopropyl)imidazole and dilute aqueous HCl solution were mixed.\r\nBy volatilizing the solvent, the white powder 1-(3-aminopropyl)imidazole chloride was obtained. After recrystallization with methanol three times, the purified white powder was dried at 333 K in a vacuum oven for 48 h.\r\nStep2: Single-crystal growth for N-(3-aminopropyl)imidazole lead chloride\r\n3.79 g Pb(Ac)2.3H2O, and 1.98g 1-(3-aminopropyl)imidazole chloride were added into an aqueous HCl solution (38%, 150mL). After heating for 50 mins, the solution became clear. By slowly evaporating the solvent at room temperature for several weeks, colorless single crystals were produced.\",Single crystal X-ray diffraction,Single-crystal X-ray diffraction was collected using Bruker D8 diffractomenter by graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å). Data reduction and empirical absorption correction was done by Crystal Clear software. The crystal structure was resolved using SHELXTL software by full-matrix least squares on F^2 using SHELXTL-97.\r\n10.1039/c8cc00786a,N-methyldabconium lead iodide,C7H15N2PbI3,\"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",C7H15N2,\"PbI3, Lead iodide\",N-methyldabconium lead (II) iodide,1,single crystal,,,,,,,,\"[N-methyldabconium]I, PbI2 and DMF\",Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals,\"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",Single crystal X-ray diffraction,Data were recorded using graphite-monochromated Mo Ka (λ = 0.71073 Å) radiation on a CCD area detector (Bruker SMART)\r\n10.1039/c8cc00786a,N-methyldabconium lead iodide,C7H15N2PbI3,\"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",C7H15N2,\"PbI3, Lead iodide\",N-methyldabconium lead (II) iodide,1,single crystal,,,,,,,,\"[N-methyldabconium]I, PbI2 and DMF\",[N-methyldabconium]PbI3,\"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",,\r\n10.1039/c8cc00786a,N-methyldabconium lead iodide,C7H15N2PbI3,\"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",C7H15N2,\"PbI3, Lead iodide\",N-methyldabconium lead (II) iodide,1,single crystal,,,,,,,,\"[N-methyldabconium]I, PbI2 and DMF\",Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals,\"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after slow evaporation at 333K after 2 weeks.\",UV-vis absorption (diffuse reflectance),The spectrum was recorded on a Shimadzu UV-3010 UV-vis-NIR spectrometer using BaSO4 as the reference of 100% reflectance.\r\n10.1039/c8cc00786a,N-methyldabconium lead iodide,C7H15N2PbI3,\"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",C7H15N2,\"PbI3, Lead iodide\",N-methyldabconium lead (II) iodide,1,single crystal,,,,,,,,\"[N-methyldabconium]I, PbI2 and DMF\",Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals,\"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",Single crystal X-ray diffraction,Data were recorded using graphite-monochromated Mo Ka (λ = 0.71073 Å) radiation on a CCD area detector (Bruker SMART)\r\n10.1039/c8cc00786a,N-methyldabconium lead iodide,C7H15N2PbI3,\"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",C7H15N2,\"PbI3, Lead iodide\",N-methyldabconium lead (II) iodide,1,single crystal,,,,,,,,\"[N-methyldabconium]I, PbI2 and DMF\",Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals,\"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",Single crystal X-ray diffraction,Data were recorded using graphite-monochromated Mo Ka (λ = 0.71073 Å) radiation on a CCD area detector (Bruker SMART)\r\n10.1039/c8cc01663a,\"2-methyl-1,5-diaminopentane lead bromide\",C6H18N2PbBr4,\"2-methyl-5-aminopentane-1-aminium tetrabromoplumbate(II), (2meptH2)PbBr4\",C6H18N2,\"PbBr4, Lead bromide\",2-methyl-5-aminopentane-1-aminium lead (II) bromide,2,single crystal,,,,,,,,\"PbAc2·3H2O, HBr solution, 2-methyl1,5-diaminopentane (2mept)\",colorless plate-like crystals,\"Step1. Fabrication of (2meptH2)PbBr4 powder\r\n\r\n0.005 mol PbAc2·3H2O (1.8967 g) was added into 20 ml 47% HBr solution. Then 0.005 mol (0.5811 g) 2-methyl1,5-diaminopentane (2mept) was dropwise added into the above solution, under stirring and heating for 5mins. After cooling down to room temperature, and drying under vacuum, (2meptH2)PbBr4 powder will be obtained. \r\n\r\nStep2:  (2meptH2)PbBr4 single crystal fabrication by temperature-lowering method. \r\n\r\nPrepare a saturated solution of (2meptH2)PbBr4 at  50 ~ 55 °C, and then preheated to  65 °C in order to form a clear solution. Decrease temperature at a rate of 1.0 °C/day, after 2 weeks colorless (2meptH2)PbBr4 will be obtained.\",Single crystal X-ray diffraction,\"SuperNova diffractometer with graphite-monochromatized Mo Kα\r\nradiation (λ = 0.71073 Å) was used to get single-crystal X-ray diffraction  at 295 K. CrystalClear software was used to do data procession. SHELXLTL software package was used to resolve crystal structure in direct methods and crystal refined in full-matrix least-squares refinements.\"\r\n10.1039/c8cc01663a,\"2-methyl-1,5-diaminopentane lead bromide\",C6H18N2PbBr4,\"2-methyl-5-aminopentane-1-aminium tetrabromoplumbate(II), (2meptH2)PbBr4\",C6H18N2,\"PbBr4, Lead bromide\",2-methyl-5-aminopentane-1-aminium lead (II) bromide,2,single crystal,,,,,,,,\"PbAc2·3H2O, HBr solution, 2-methyl1,5-diaminopentane (2mept)\",colorless crystals,\"Step1. Fabrication of (2meptH2)PbBr4 powder - 0.005 mol PbAc2·3H2O (1.8967 g) was added into 20 ml 47% HBr solution. Then 0.005 mol (0.5811 g) 2-methyl1,5-diaminopentane (2mept) was dropwisely added to the above solution, under stirring and heating for 5 mins. After cooling down to room temperature, and dried under vacuum, (2meptH2)PbBr4 powder was obtained. Step2: (2meptH2)PbBr4 single crystal fabrication - prepare a saturated solution of (2meptH2)PbBr4 at 50 ~ 55 °C, and then preheated to 65 °C in order to form a clear solution. Decrease temperature at a rate of 1.0 °C/day, after 2 weeks colorless (2meptH2)PbBr4 will be obtained.\",Photoluminescence,Edinburgh FLS980 fluorescence spectrometer was used to get emission spectra.\r\n10.1039/c8cc01663a,\"2-methyl-1,5-diaminopentane lead bromide\",C6H18N2PbBr4,\"2-methyl-5-aminopentane-1-aminium tetrabromoplumbate(II), (2meptH2)PbBr4\",C6H18N2,\"PbBr4, Lead bromide\",2-methyl-5-aminopentane-1-aminium lead (II) bromide,2,single crystal,,,,,,,,\"PbAc2·3H2O, HBr solution, 2-methyl1,5-diaminopentane (2mept)\",colorless crystals,\"Step1. Fabrication of (2meptH2)PbBr4 powder -  0.005 mol PbAc2·3H2O (1.8967 g) was added into 20 ml 47% HBr solution. Then 0.005 mol (0.5811 g) 2-methyl1,5-diaminopentane (2mept) was dropwisely added to the above solution, under stirring and heating for 5 mins. After cooling down to room temperature, and dried under vacuum, (2meptH2)PbBr4 powder was obtained. \r\nStep2: (2meptH2)PbBr4 single crystal fabrication - prepare a saturated solution of (2meptH2)PbBr4 at 50 ~ 55 °C, and then preheated to 65 °C in order to form a clear solution. Decrease temperature at a rate of 1.0 °C/day, after 2 weeks colorless (2meptH2)PbBr4 will be obtained.\",UV-vis absorption,Perkin-Elmer Lambda 900 UV–Vis–NIR spectrophotometer was used to get the absorption spectrum at room temperature. BaSO4 was used as the 100% reflectance reference.\r\n10.1039/C8SC03863E,Bis(2-ethyl-hexylammonium) lead iodide,C16H40N2PbI4,\"bis(2-ethyl-1-hexanaminium) tetraiodoplumbate(II), (2-Et-ha)2PbI4\",C8H20N,\"PbI4, Lead iodide\",bis(2-ethyl-1-hexanaminium) lead (II) iodide,2,single crystal,,,,,,,,\"2-Ethyl-1-hexylamine (2-Et-ha, 98%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",clear orange plate-like crystal,\"2-Et-ha∙HI salt was synthesized by adding a stoichiometric volume of HI into 2-Ethyl-1-hexylamine in a cold water bath, evaporating water at 150 ˚C on a hot plate and vacuum drying at 150 ˚C at 40 mtorr for a week. Thin plate-like (2-Et-ha)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-ha∙HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",Single crystal X-ray Diffraction,Data were collected using Bruker D8 ADVANCE Series II diffractometer using Mo Kα radiation (= 0.71073 Å).\r\n10.1039/C8SC03863E,1-methyl-hexylammonium lead iodide,C14H36N2PbI4,\"1-methyl-hexanaminium tetraiodoplumbate(II), [C14H36N2]PbI4, (1-Me-ha)2PbI4\",C7H18N,\"PbI4, Lead iodide\",1-methyl-hexanaminium lead (II) iodide,2,single crystal,,,,,,,,\"2-Aminoheptane (1-Me-ha, 99%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",Clear light orange plate-like crystals,\"1Me-ha∙HI salt was synthesized by adding a stoichiometric volume of HI into  2-Aminoheptane in a cold water bath, evaporating water at 150 ˚C on a hot plate and vacuum drying at 150 ˚C at 40 mtorr for a week. Thin plate-like (1-Me-ha)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-ha∙HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",Single crystal X-ray Diffraction,Data were collected using Bruker D8 ADVANCE Series II diffractometer using Mo Kα radiation (= 0.71073 Å).\r\n10.1039/C8SC03863E,bis(sec-butylammonium) lead iodide,C8H24N2PbI4,\"1-methyl-1-propanaminium tetraiodoplumbate(II), (1-Me-pa)2PbI4\",C4H12N,\"PbI4, Lead iodide\",1-methyl-1-propanaminium lead (II) iodide,2,single crystal,,,,,,,,\"sec-butylamine (1-Me-pa, 99%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",metallic orange block,\"1-Me-pa∙HI salt was synthesized by adding a stoichiometric volume of HI into sec-butylamine in a cold water bath, evaporating water at 150 ˚C on a hot plate and vacuum drying at 150 ˚C at 40 mtorr for a week. Thin plate-like (1-Me-pa)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-pa∙HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",Single crystal X-ray Diffraction,Data were collected using Rigaku XtaLAB Synergy-S diffractometer using Mo Kα radiation (= 0.71073 Å).\r\n10.1039/C8SC03863E,bis(1-methyl-butylammonium) lead iodide,C10H30N2PbI4,\"1-methyl-1-butanaminium tetraiodoplumbate(II), (1-Me-ba)2PbI4\",C5H15N,\"PbI4, Lead iodide\",1-methyl-1-butanaminium lead (II) iodide,2,single crystal,,,,,,,,\"2-Aminopentane (1-Me-ba, 97%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",clear orange plate-like crystals,\"1-Me-ba∙HI salt was synthesized by adding a stoichiometric volume of HI into 2-Aminopentane in a cold water bath, evaporating water at 150 ˚C on a hot plate and vacuum drying at 150 ˚C at 40 mtorr for a week. Thin plate-like (1-Me-ba)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-ba∙HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",Single crystal X-ray Diffraction,Data were collected using Bruker D8 ADVANCE Series II diffractometer using Mo Kα radiation (= 0.71073 Å).\r\n10.1039/c9ce00591a,Bis(methylammonium) manganese chloride,(CH3NH3)2MnCl4,\"MA2MnCl4, bis(methanaminium) tetrachloromanganate(II)\",CNH6,\"MnCl4, Manganese chloride\",bis(methanaminium) manganese chloride,2,single crystal,,,,,,,,\"MnCl2 (≥99%, A.R. Aladdin), methylammonium chloride (MACl), DMF, DMSO\",MA2MnCl4 single crystals,\"The single-crystal hybrid perovskite MA2MnCl4 was synthesized from two solutions. The first solution contained a mixture of MnCl2 and MACl and was dissolved in both DMF and DMSO polar solvents. The solution was then heated to  90 °C, which eventually yielded the product. The second method that was used to produce (CH3NH3)2MnCl4 by using a strong acid as the solvent (HCl) was also heated to yield the crystals of the product.\",Thermogravimetric (TG) analysis and DSC,TGA was performed by using a STA449C (Netzsch) device.\r\n10.1039/c9ce00591a,Bis(methylammonium) manganese chloride,(CH3NH3)2MnCl4,\"MA2MnCl4, bis(methanaminium) tetrachloromanganate(II)\",CNH6,\"MnCl4, Manganese chloride\",bis(methanaminium) manganese chloride,2,single crystal,,,,,,,,\"MnCl2 (≥99%, A.R. Aladdin), methylammonium chloride (MACl), DMF, DMSO\",MA2MnCl4 single crystals,\"The single-crystal hybrid perovskite MA2MnCl4 was synthesized from two solutions. The first solution contained a mixture of MnCl2 and MACl and was dissolved in both DMF and DMSO polar solvents. The solution was then heated to 90 °C, which eventually yielded the product. The second method that was used to produce (CH3NH3)2MnCl4 by using a strong acid as the solvent (HCl) was also heated to yield the crystals of the product.\",UV-Vis absorption,A UV-Vis absorption spectrum was recorded using a UV-2550 spectrometer.\r\n10.1039/c9ce00591a,Bis(methylammonium) manganese chloride,(CH3NH3)2MnCl4,\"MA2MnCl4, bis(methanaminium) tetrachloromanganate(II)\",CNH6,\"MnCl4, Manganese chloride\",bis(methanaminium) manganese chloride,2,single crystal,,,,,,,,\"MnCl2 (≥99%, A.R. Aladdin), methylammonium chloride (MACl), DMF, DMSO\",MA2MnCl4 single crystals,\"The single-crystal hybrid perovskite MA2MnCl4 was synthesized from two solutions. The first solution contained a mixture of MnCl2 and MACl and was dissolved in both DMF and DMSO polar solvents. The solution was then heated to 90 °C, which eventually yielded the product. The second method that was used to produce (CH3NH3)2MnCl4 by using a strong acid as the solvent (HCl) was also heated to yield the crystals of the product.\",Photoluminescence,\"FLS980 of Edinburgh Instruments was used to record the spectra. Lake Shore Cryotronics, Model 336 with ARS-4HW Compressor was used to control the temperature.\"\r\n10.1039/c9dt00945k,\"N,N-dimethylethanolammonium cadmium chloride\",C4H12NOCdCl3,\"N,N-dimethylethanolaminium trichlorocadmate(II), (DMEA)CdCl3, (C4H12NO)CdCl3\",C4H12NO,\"CdCl3, Cadmium chloride\",\"N,N-dimethylethanolaminium cadmium chloride\",1,single crystal,,,,,,,,\"N,N-dimethylethanolamine (DMEA), CdCl2 and HCl (37% concentrated)\",colorless strip (DMEA)CdCl3 crystals,\"A solution mixture of DMEA (10 mmol), CdCl2 (10 mmol), and HCl (20 mmol) was slowly evaporated at room temperature for two weeks.\",Single crystal X-ray diffraction,Data were recorded using Rigaku CCD diffractometer with Mo-Kα radiation (λ = 0.71073 Å)\r\n10.1039/c9dt00945k,\"N,N-dimethylethanolammonium cadmium chloride\",C4H12NOCdCl3,\"N,N-dimethylethanolaminium trichlorocadmate(II), (DMEA)CdCl3, (C4H12NO)CdCl3\",C4H12NO,\"CdCl3, Cadmium chloride\",\"N,N-dimethylethanolaminium cadmium chloride\",1,single crystal,,,,,,,,\"N,N-dimethylethanolamine (DMEA), CdCl2 and HCl (37% concentrated)\",colorless strip (DMEA)CdCl3 crystals,\"A solution mixture of DMEA (10 mmol), CdCl2 (10 mmol), and HCl (20 mmol) was slowly evaporated at room temperature for two weeks.\",Infrared absorption,The spectrum was recorded using a Shimadzu model IR-60 spectrometer.\r\n10.1039/c9dt00945k,\"N,N-dimethylethanolammonium cadmium chloride\",C4H12NOCdCl3,\"N,N-dimethylethanolaminium trichlorocadmate(II), (DMEA)CdCl3, (C4H12NO)CdCl3\",C4H12NO,\"CdCl3, Cadmium chloride\",\"N,N-dimethylethanolaminium cadmium chloride\",1,single crystal,,,,,,,,\"N,N-dimethylethanolamine (DMEA), CdCl2 and HCl (37% concentrated)\",colorless strip (DMEA)CdCl3 crystals,\"A solution mixture of DMEA (10 mmol), CdCl2 (10 mmol), and HCl (20 mmol) was slowly evaporated at room temperature for two weeks.\",Single crystal X-ray diffraction,Data were recorded using Rigaku CCD diffractometer with Mo-Kα radiation (λ = 0.71073 Å)\r\n10.1039/c9mh00366e,Bis(aminoethyl)-thiophene lead chloride,C8H16N2SPbCl4,\"2,5-bis(aminoethyl)-thiophene tetrachloroplumbate(II), AE1TPbCl4, (AET)PbCl4, AETPbCl4, C8H16SN2PbCl4\",C8H16N2S,\"PbCl4, Lead chloride\",\"2,5-bis(aminoethyl)-thiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-thiophene lead iodide,C8H16N2SPbI4,\"2,5-bis(aminoethyl)-thiophene tetraiodoplumbate(II), AE1TPbI4, (AET)PbI4, AETPbI4, C8H16SN2PbI4\",C8H16N2S,\"PbI4, Lead iodide\",\"2,5-bis(aminoethyl)-thiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-bithiophene lead chloride,C12H18N2S2PbCl4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrachloroplumbate(II), AE2TPbCl4, (AEDT)PbCl4, AEDTPbCl4, C12H18S2N2PbCl4\",C12H18N2S2,\"PbCl4, Lead chloride\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-bithiophene lead iodide,C12H18N2S2PbI4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",C12H18N2S2,\"PbI4, Lead iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-terthiophene lead chloride,C16H20N2S3PbCl4,\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrachloroplumbate(II), AE3TPbCl4, (AETT)PbCl4, AETTPbCl4, C16H20S3N2PbCl4\",C16H20N2S3,\"PbCl4, Lead chloride\",\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-terthiophene lead iodide,C16H20N2S3PbI4,\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetraiodoplumbate(II), AE3TPbI4, (AETT)PbI4, AETTPbI4, C16H20S3N2PbI4\",C16H20N2S3,\"PbI4, Lead iodide\",\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-quinquethiophene lead chloride,C24H24N2S5PbCl4,\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrachloroplumbate(II), AE5TPbCl4, (AE5T)PbCl4, C24H24S5N2PbCl4\",C24H24N2S5,\"PbCl4, Lead chloride\",\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-quinquethiophene lead iodide,C24H24N2S5PbI4,\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetraiodoplumbate(II), AE5TPbI4, (AE5T)PbI4, C24H24S5N2PbI4\",C24H24N2S5,\"PbI4, Lead iodide\",\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-thiophene lead chloride,C8H16N2SPbCl4,\"2,5-bis(aminoethyl)-thiophene tetrachloroplumbate(II), AE1TPbCl4, (AET)PbCl4, AETPbCl4, C8H16SN2PbCl4\",C8H16N2S,\"PbCl4, Lead chloride\",\"2,5-bis(aminoethyl)-thiophene lead(II) chloride\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-thiophene lead iodide,C8H16N2SPbI4,\"2,5-bis(aminoethyl)-thiophene tetraiodoplumbate(II), AE1TPbI4, (AET)PbI4, AETPbI4, C8H16SN2PbI4\",C8H16N2S,\"PbI4, Lead iodide\",\"2,5-bis(aminoethyl)-thiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-bithiophene lead chloride,C12H18N2S2PbCl4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrachloroplumbate(II), AE2TPbCl4, (AEDT)PbCl4, AEDTPbCl4, C12H18S2N2PbCl4\",C12H18N2S2,\"PbCl4, Lead chloride\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-bithiophene lead iodide,C12H18N2S2PbI4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",C12H18N2S2,\"PbI4, Lead iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-terthiophene lead chloride,C16H20N2S3PbCl4,\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrachloroplumbate(II), AE3TPbCl4, (AETT)PbCl4, AETTPbCl4, C16H20S3N2PbCl4\",C16H20N2S3,\"PbCl4, Lead chloride\",\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-terthiophene lead iodide,C16H20N2S3PbI4,\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetraiodoplumbate(II), AE3TPbI4, (AETT)PbI4, AETTPbI4, C16H20S3N2PbI4\",C16H20N2S3,\"PbI4, Lead iodide\",\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-quinquethiophene lead chloride,C24H24N2S5PbCl4,\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrachloroplumbate(II), AE5TPbCl4, (AE5T)PbCl4, C24H24S5N2PbCl4\",C24H24N2S5,\"PbCl4, Lead chloride\",\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,Bis(aminoethyl)-quinquethiophene lead iodide,C24H24N2S5PbI4,\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetraiodoplumbate(II), AE5TPbI4, (AE5T)PbI4, C24H24S5N2PbI4\",C24H24N2S5,\"PbI4, Lead iodide\",\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) iodide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1039/c9mh00366e,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead chloride\",C20H22N2S4PbCl4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",C20H22N2S4,\"PbCl4, Lead chloride\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",2,film,,,,,,,,\"AE4T*2HCl, PbCl2\",AE4TPbCl4 film on glass or quartz,Thin film growth by RIR-MAPLE method from a 2 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films annealed in nitrogen at 125 C for 5 min after deposition.,UV-vis absorption,UV-vis spectra were collected using a Shimadzu UV-3600 spectrophotometer using a blank substrate as reference.\r\n10.1039/c9mh00366e,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead chloride\",C20H22N2S4PbCl4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",C20H22N2S4,\"PbCl4, Lead chloride\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",2,film,,,,,,,,\"AE4T*2HCl, PbCl2\",AE4TPbCl4 film on glass or quartz,Thin film growth by RIR-MAPLE method from a 2 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films annealed in nitrogen at 125 C for 5 min after deposition.,Photoluminescence,\"Steady-state PL spectra were recorded using Edinburgh Instruments FS920 fluorimeter that was equipped with a 450 W xenon arc lamp as the excitation source, and a Peltier-cooled Hamamatsu R2658P photomultiplier tube.\"\r\n10.1039/c9mh00366e,Bis(aminoethyl)-bithiophene lead iodide,C12H18N2S2PbI4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",C12H18N2S2,\"PbI4, Lead iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",2,film,,,,,,,,\"AE2T*2HI, PbI2\",AE2TPbI4 film on glass or quartz,Thin film growth by RIR-MAPLE method from a 4 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 150 C for 10 min after deposition.,UV-vis absorption,UV-vis spectra were collected using a Shimadzu UV-3600 spectrophotometer using a blank substrate as reference.\r\n10.1039/c9mh00366e,Bis(aminoethyl)-bithiophene lead iodide,C12H18N2S2PbI4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",C12H18N2S2,\"PbI4, Lead iodide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",2,film,,,,,,,,\"AE2T*2HI, PbI2\",AE2TPbI4 film on glass or quartz,Thin film growth by RIR-MAPLE method from a 4 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 150 C for 10 min after deposition.,Photoluminescence,\"Steady-state PL spectra were recorded using Edinburgh Instruments FS920 fluorimeter that was equipped with a 450 W xenon arc lamp as the excitation source, and a Peltier-cooled Hamamatsu R2658P photomultiplier tube.\"\r\n10.1039/c9mh00366e,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",C20H22N2S4PbI4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",C20H22N2S4,\"PbI4, Lead iodide\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",2,film,,,,,,,,\"AE4T*2HI, PbI2\",AE4TPbI4 film on glass or quartz,Thin film growth by RIR-MAPLE method from a 4 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 200 C for 30 min after deposition.,UV-vis absorption,UV-vis spectra were collected using a Shimadzu UV-3600 spectrophotometer using a blank substrate as reference.\r\n10.1039/c9mh00366e,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",C20H22N2S4PbI4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",C20H22N2S4,\"PbI4, Lead iodide\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",2,film,,,,,,,,\"AE4T*2HI, PbI2\",AE2TPbI4 film on glass or quartz,Thin film growth by RIR-MAPLE method from a 8 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 150 C for 10 min after deposition.,Photoluminescence,\"Steady-state PL spectra were recorded using Edinburgh Instruments FS920 fluorimeter that was equipped with a 450 W xenon arc lamp as the excitation source, and a Peltier-cooled Hamamatsu R2658P photomultiplier tube.\"\r\n10.1039/d1nr06899g,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,FHI-aims,DFT,PBE+TS,2*8*8,atomic ZORA,tight,force convergence 5e-3 eV/AA,,,,,\r\n10.1039/d1nr06899g,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",Exfoliated single crystal flakes of (PEA)2PbI4.,\"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 °C. The solution is then slowly cooled to room temperature at a rate of 2 °C h−1, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",Reflection mode and transmission mode ellipsometry,\"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45° to 75° using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from −10° to 70°. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\"\r\n10.1039/d1nr06899g,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",Exfoliated single crystal flakes of (PEA)2PbI4.,\"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 °C. The solution is then slowly cooled to room temperature at a rate of 2 °C h−1, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",Reflection mode and transmission mode ellipsometry,\"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45° to 75° using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from −10° to 70°. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\"\r\n10.1039/d1nr06899g,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",Exfoliated single crystal flakes of (PEA)2PbI4.,\"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 °C. The solution is then slowly cooled to room temperature at a rate of 2 °C h−1, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",Reflection mode and transmission mode ellipsometry,\"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45° to 75° using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from −10° to 70°. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\"\r\n10.1039/d1nr06899g,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,3,single crystal,,,,,,,,\"200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",Exfoliated single crystal flakes of (PEA)2PbI4.,\"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 μL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 °C. The solution is then slowly cooled to room temperature at a rate of 2 °C h−1, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",Reflection mode and transmission mode ellipsometry,\"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45° to 75° using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from −10° to 70°. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\"\r\n10.1039/d1nr06899g,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,FHI-aims,Spin-orbit coupled hybrid DFT,\"HSE06 functional; exchange mixing parameter: 0.25, screening parameter: 0.11 (Bohr radii)^(-1)\",3x7x7,Spin-orbit coupling included as follows: Self-consistent scalar relativity (atomic zero-order regular approximation) with spin-orbit coupling applied non-selfconsistently in the energy band structure calculation.,\"All-electron; \"\"intermediate\"\" numerical settings and basis sets.\",\"Note that DFT-computed energy band gap values, even at the level of DFT-HS06+SOC, are not intended to capture the experimentally correct fundamental gap with quantitative accuracy. Rather, they are collected be comparable to other computational band gaps at the same level of theory in order to capture trends between different sources.\",,,,,\r\n10.1039/d1nr06899g,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,FHI-aims,Spin-orbit coupled hybrid DFT,\"HSE06 functional; exchange mixing parameter: 0.25, screening parameter: 0.11 (Bohr radii)^(-1)\",3x7x7,Spin-orbit coupling included as follows: Self-consistent scalar relativity (atomic zero-order regular approximation) with spin-orbit coupling applied non-selfconsistently in the energy band structure calculation.,\"All-electron; \"\"intermediate\"\" numerical settings and basis sets.\",\"Note that DFT-computed energy band gap values, even at the level of DFT-HS06+SOC, are not intended to capture the experimentally correct fundamental gap with quantitative accuracy. Rather, they are collected be comparable to other computational band gaps at the same level of theory in order to capture trends between different sources.\",,,,,\r\n10.1063/1.453467,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",Colorless MAPbCl3 crystals,CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.,Temperature-dependent Guinier-Simon photograph,Not specified.\r\n10.1063/1.453467,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",Colorless MAPbCl3 crystals,CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.,Temperature-dependent Guinier-Simon photograph,Not specified.\r\n10.1063/1.453467,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",Colorless MAPbCl3 crystals,CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.,Temperature-dependent Guinier-Simon photograph,Not specified.\r\n10.1063/1.453467,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",Orange MAPbBr3 crystals,CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.,temperature-dependent Guinier-Simon photograph,No experimental details reported. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",Orange MAPbBr3 crystals,CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.,temperature-dependent Guinier-Simon photograph,No experimental details reported. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",Orange MAPbBr3 crystals,CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.,temperature-dependent Guinier-Simon photograph,No experimental details reported. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",Orange MAPbBr3 crystals,CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.,temperature-dependent Guinier-Simon photograph,No experimental details reported. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",Black MAPbI3 crystals,CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.,temperature-dependent Guinier-Simon photograph,No experimental details reported. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",Black MAPbI3 crystals,CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.,temperature-dependent Guinier-Simon photograph,No experimental details reported. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",Black MAPbI3 crystals,CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.,temperature-dependent Guinier-Simon photograph,No experimental details reported. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",Colorless MAPbCl3 crystals,CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00°C to room temperature to obtain the colorless crystals.,Temperature-dependent Guinier-Simon photograph,No method specified. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",Orange MAPbBr3 crystals,CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00°C to room temperature to obtain the orange crystals.,Temperature-dependent Guinier-Simon photograph,No method specified. Refer to Page 6374 Table I.\r\n10.1063/1.453467,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",Black MAPbI3 crystals,CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00°C to 40°C to obtain the black crystals.,Temperature-dependent Guinier-Simon photograph,No method specified. Refer to Page 6374 Table I.\r\n10.1063/1.4947305,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,CRYSTAL09,DFT,PBESOL-D2,,,cc-p VDZ,,,,,,\r\n10.1063/1.4947305,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,Crystal09,DFT,PBESOL-D2,,,cc-p VDZ,,,,,,\r\n10.1063/1.5083792,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,N/A,MAPbI3 Thin-film on Si,Not described.,Absorption spectra,\"Absorption spectra was obtained for 350–450 nm-thick perovskite thin-films on glass from room temperature down to 5 K. Samples were mounted in a liquid helium bath cryostat and illuminated with a halogen lamp. Absorption spectra were obtained using a 0.275m focal-length monochromator with a 150 lines/mm or 300 lines/mm grating and detected by a charge-coupled device (CCD) camera.\r\n\r\nA generalized version of the well-known Elliott formula was used to deduce the exciton binding energies and band gaps at successive temperatures.\r\n\r\nRefer to Fig. 2&3.\"\r\n10.1103/PhysRevApplied.10.041001,Cesium silver bismuth chloride,Cs2AgBiCl6,Dicesium trichloroargentate(I) µ-dichloro trichlorobismuthate(III),None,\"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",,3,single crystal,VASP,DFT,PBE,,,,,,,,,\r\n10.1103/PhysRevB.106.094306,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,film,,,,,,,,\"CsBr, PbBr2, dimethyl sulfoxide (DMSO\",CsPbBr3 thin film,\"A precursor solution, (0.5 M), was made by mixing CsBr (Sigma Aldrich, 0.21 grams), PbBr2 (Sigma Aldrich, 0.37 grams), and dimethyl sulfoxide (DMSO) (2 mL). This solution was then spin cast at 3000 RPM on cleaned glass for 60 seconds. It was then annealed at 106 °C for 20 minutes. The resulting film of CsPbBr3 was about 100 nm thick.\",Photoluminescence measurement at T = 100 K,The CsPbBr3 thin film is excited at 447 nm with power at 0.5 mW and the intensity of each photon energy emission is measured. This test was performed at temperature T = 100 K.\r\n10.1103/PhysRevB.106.094306,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,film,,,,,,,,\"CsBr, PbBr2, dimethyl sulfoxide (DMSO\",CsPbBr3 thin film,\"A precursor solution, (0.5 M), was made by mixing CsBr (Sigma Aldrich, 0.21 grams), PbBr2 (Sigma Aldrich, 0.37 grams), and dimethyl sulfoxide (DMSO) (2 mL). This solution was then spin cast at 3000 RPM on cleaned glass for 60 seconds. It was then annealed at 106 °C for 20 minutes. The resulting film of CsPbBr3 was about 100 nm thick.\",Photoluminescence measurement at T = 50 K,The CsPbBr3 thin film is excited at 447 nm with power at 0.5 mW and the intensity of each photon energy emission is measured. This test was performed at temperature of 50 K.\r\n10.1103/PhysRevB.106.094306,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,film,,,,,,,,\"CsBr, PbBr2, dimethyl sulfoxide (DMSO\",CsPbBr3 thin film,\"A precursor solution, (0.5 M), was made by mixing CsBr (Sigma Aldrich, 0.21 grams), PbBr2 (Sigma Aldrich, 0.37 grams), and dimethyl sulfoxide (DMSO) (2 mL). This solution was then spin cast at 3000 RPM on cleaned glass for 60 seconds. It was then annealed at 106 °C for 20 minutes. The resulting film of CsPbBr3 was about 100 nm thick.\",Photoluminescence measurement at T = 10 K,The CsPbBr3 thin film is excited at 447 nm with power at 0.5 mW and the intensity of each photon energy emission is measured. This test was performed at temperature T = 10 K.\r\n10.1103/PhysRevB.70.205330,Bis(phenylethyammonium) lead iodide (Bi-doped),(C6H5C2H4NH3)2PbI4,\"PEA lead iodide (Bi-doped), PEA PbI (Bi-doped), Phenylethylammonium lead iodide, Bis(phenylethyammonium) tetraiodoplumbate(II) (Bi-doped)\",C8H12N,PbI4,bis(1-phenyl-2-aminoethane) lead (II) tetraiodide (Bi-doped),2,single crystal,,,,,,,,\"PbI2, BiI3, C6H5C2H4NH3I\",\"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",Photoluminescence,\"As a detector, a charge-coupled device (CCD) camera cooled by liquid nitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV.\"\r\n10.1103/PhysRevB.70.205330,Bis(phenylethyammonium) lead iodide (Bi-doped),(C6H5C2H4NH3)2PbI4,\"PEA lead iodide (Bi-doped), PEA PbI (Bi-doped), Phenylethylammonium lead iodide, Bis(phenylethyammonium) tetraiodoplumbate(II) (Bi-doped)\",C8H12N,PbI4,bis(1-phenyl-2-aminoethane) lead (II) tetraiodide (Bi-doped),2,single crystal,,,,,,,,\"PbI2, BiI3, C6H5C2H4NH3I\",\"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",Photoluminescence excitation,\"As a detector, a charge-coupled device (CCD) camera cooled by liquid nitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV. PLE spectra represent detected PL at 1.4 eV.\"\r\n10.1103/PhysRevB.70.205330,Bis(phenylethyammonium) lead iodide (Bi-doped),(C6H5C2H4NH3)2PbI4,\"PEA lead iodide (Bi-doped), PEA PbI (Bi-doped), Phenylethylammonium lead iodide, Bis(phenylethyammonium) tetraiodoplumbate(II) (Bi-doped)\",C8H12N,PbI4,bis(1-phenyl-2-aminoethane) lead (II) tetraiodide (Bi-doped),2,single crystal,,,,,,,,\"PbI2, BiI3, C6H5C2H4NH3I\",\"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",Optical absorption measurement,\"As a detector, a charge-coupled device (CCD) camera cooled by liquid nitrogen and equipped with a polychromator was utilized. A halogen lamp was used as a probe light for optical absorption measurements.\"\r\n10.1103/PhysRevB.70.205330,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2, BiI3, C6H5C2H4NH3I\",\"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",PL-spectroscopy,\"As a detector, a charge-coupled device (CCD) camera cooled by liquid\r\nnitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV.\"\r\n10.1103/PhysRevB.70.205330,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2, BiI3, C6H5C2H4NH3I\",\"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",PLE-spectroscopy,\"As a detector, a charge-coupled device (CCD) camera cooled by liquid\r\nnitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV. PLE spectra represent detected PL at 2.35 eV.\"\r\n10.1103/PhysRevB.70.205330,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2, BiI3, C6H5C2H4NH3I\",\"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",optical absorption measurement,\"As a detector, a charge-coupled device (CCD) camera cooled by liquid\r\nnitrogen and equipped with a polychromator was utilized.  A halogen\r\nlamp was used as a probe light for optical absorption measurements.\"\r\n10.1103/PhysRevB.93.094105,ammonium tin iodide,NH4SnI3,\"aminium triiodostannate(II), Ammonium Tin Iodide\",NH4,\"SnI3, Tin iodide\",aminium tin (II) iodide,3,single crystal,VASP,density functional theory,HSE06,7 × 7 × 7,spin-orbit coupling included,,,,,,,\r\n10.1103/PhysRevLett.121.146401,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,FHI-aims,density functional theory,PBE,,atomic ZORA,tight,tight,,,,,\r\n10.1103/PhysRevLett.121.146401,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,FHI-aims,density functional theory,PBE with Tkatchenko-Scheffler van der Waals correction,,atomic ZORA,tight,tight,,,,,\r\n10.1103/PhysRevLett.121.146401,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,FHI-aims,density functional theory,PBE with many-body dispersion (range-separated MBD@rsSCS),,atomic ZORA,tight,tight,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead bromide\",C20H22N2S4PbBr4,\"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tetrabromoplumbate(II)\",C20H22N2S4,\"PbBr4, Lead bromide\",\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead(II) bromide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-thiophene lead bromide,C8H16N2SPbBr4,\"2,5-bis(aminoethyl)-thiophene tetrabromoplumbate(II), AE1TPbBr4, C8H16SN2PbBr4\",C8H16N2S,\"PbBr4, Lead bromide\",\"2,5-bis(aminoethyl)-thiophene lead(II) bromide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-bithiophene lead bromide,C12H18N2S2PbBr4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrabromoplumbate(II), AE2TPbBr4, (AEBT)PbBr4, AEBTPbBr4, C12H18S2N2PbBr4\",C12H18N2S2,\"PbBr4, Lead bromide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) bromide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-terthiophene lead bromide,C16H20N2S3PbBr4,\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrabromoplumbate(II), AE3TPbBr4, (AE3T)PbBr4, C16H20S3N2PbBr4\",C16H20N2S3,\"PbBr4, Lead bromide\",\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) bromide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead chloride\",C20H22N2S4PbCl4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",C20H22N2S4,\"PbCl4, Lead chloride\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",C20H22N2S4PbI4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",C20H22N2S4,\"PbI4, Lead iodide\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-quinquethiophene lead bromide,C24H24N2S5PbBr4,\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrabromoplumbate(II), AE5TPbBr4, C24H24S5N2PbBr4\",C24H24N2S5,\"PbBr4, Lead bromide\",\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) bromide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,with spin-orbit coupling,,,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead bromide\",C20H22N2S4PbBr4,\"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tetrabromoplumbate(II)\",C20H22N2S4,\"PbBr4, Lead bromide\",\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead(II) bromide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead bromide\",C20H22N2S4PbBr4,\"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tetrabromoplumbate(II)\",C20H22N2S4,\"PbBr4, Lead bromide\",\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead(II) bromide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-thiophene lead bromide,C8H16N2SPbBr4,\"2,5-bis(aminoethyl)-thiophene tetrabromoplumbate(II), AE1TPbBr4, C8H16SN2PbBr4\",C8H16N2S,\"PbBr4, Lead bromide\",\"2,5-bis(aminoethyl)-thiophene lead(II) bromide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",1x2x2,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-bithiophene lead bromide,C12H18N2S2PbBr4,\"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrabromoplumbate(II), AE2TPbBr4, (AEBT)PbBr4, AEBTPbBr4, C12H18S2N2PbBr4\",C12H18N2S2,\"PbBr4, Lead bromide\",\"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) bromide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-terthiophene lead bromide,C16H20N2S3PbBr4,\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrabromoplumbate(II), AE3TPbBr4, (AE3T)PbBr4, C16H20S3N2PbBr4\",C16H20N2S3,\"PbBr4, Lead bromide\",\"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) bromide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead chloride\",C20H22N2S4PbCl4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",C20H22N2S4,\"PbCl4, Lead chloride\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,Bis(aminoethyl)-quinquethiophene lead bromide,C24H24N2S5PbBr4,\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrabromoplumbate(II), AE5TPbBr4, C24H24S5N2PbBr4\",C24H24N2S5,\"PbBr4, Lead bromide\",\"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) bromide\",3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",,atomic ZORA with spin-orbit-coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",C20H22N2S4PbI4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",C20H22N2S4,\"PbI4, Lead iodide\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",2,single crystal,,,,,,,,\"PbI2 (99.999% trace metal basis), HI (57 wt. % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), N,N-Dimethylformamide (anhydrous, 99.8%, Sigma-Aldrich), 2-butanol (99.5%, VWR International)\",Orange crystals,\"Synthesize AE4T·HI in the lab. References [1-3]\r\n\r\nDissolve 2 mg PbI2 and 3 mg AE4T·HI in 0.7 ml DMF with a drop of HI. Then, layer 2 ml 2-butanol on top of the solution (SI Figure S8a). In the experiment, the target crystals came out after several days (Figure S8b).\",Single crystal X-ray diffraction,Bruker D8 ADVANCE Series II at room temperature.\r\n10.1103/PhysRevLett.121.146401,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,FHI-aims,density functional theory,PBE with Tkatchenko-Scheffler van der Waals correction,1x2x2,atomic ZORA,tight,tight,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead bromide\",C20H22N2S4PbBr4,\"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene tetrabromoplumbate(II)\",C20H22N2S4,\"PbBr4, Lead bromide\",\"5,5‘‘‘-bis(aminoethyl)-2,2‘:5‘,2‘‘:5‘‘,2‘‘‘-quaterthiophene lead(II) bromide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1103/PhysRevLett.121.146401,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",C20H22N2S4PbI4,\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",C20H22N2S4,\"PbI4, Lead iodide\",\"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",2,single crystal,FHI-aims,density functional theory,\"HSE06 α = 0.25, ω = 0.11/bohr\",3x3x3,atomic ZORA with spin-orbit coupling,tight,,,,,,\r\n10.1107/S0108270106009127,Tetrakis(3-phenylpropylammonium) lead iodide,C36H52N4Pb3I10,\"tetrakis(1-phenylpropane-3-aminium) decaiodo triplumbate(II), (C9H14N)4Pb3I10\",C9H14N,\"Pb3I10, Lead iodide\",tetrakis(1-phenylpropane-3-aminium) lead iodide,2,single crystal,,,,,,,,\"PbO, 3-phenylpropylamine, HI\",Yellow rectangular crystals,\"Dissolve PbO (0.184 g, 0.824 mmol) and 3-phenylpropylamine (0.167 g, 1.23 mmol) in HI (3 ml) and heat to form a clear solution. Slowly cool to room temperature to form yellow crystals.\",Single-crystal X-ray diffraction,Bruker SMART CCD area-detector diffractometer with Mo Kα radiation\r\n10.1107/S0108270106016167,Bis­(tert-butyl­ammonium) lead iodide dihydrate,C8H24N2[PbI3]I 2H2O,\"bis¬≠(2-methylpropane-2-aminium) tetraiodoplumbate(II) dihydrate, (C4H12N)2[PbI3]I 2H2O\",C4H12N,\"[PbI3]I, Lead iodide\",bis­(2-methylpropane-2-aminium) lead (II) iodide dihydrate,1,single crystal,,,,,,,,\"PbI2, HI, C(CH3)3NH2\",Yellow needle-like crystal,\"Dissolve PbI2 (0.126 g, 0.273 mmol) in 47% HI (2 ml) in a sample vial. Thereafter, add C(CH3)3NH2 (0.050 g, 0.684 mmol) and dissolve the resulting precipitate by refluxing for 12 h at 363 K. Slowly cool the solution to room temperature at a rate of 2 K/h.\",Single-crystal X-ray diffraction,Bruker SMART CCD area-detector diffractometer with Mo Kα radiation.\r\n10.1107/S0108270106039746,\"1,4-phenyldiammonium lead iodide dihydrate\",C6H10N2PbI4-2H2O,\"1,4-phenyldiaminium tetraiodoplumbate(II) dihydrate, H3NC6H4NH3PbI4-2H2O\",C6H10N2,\"PbI4, Lead iodide\",\"1,4-phenyldiaminium lead iodide dihydrate\",1,single crystal,,,,,,,,\"PbI2, HI, NH2C6H4NH2\",Brown polyhedral crystals,\"Dissolve PbI2 (0.200 g, 0.434 mmol) in 47% HI (7 ml) in a test tube. Add NH2C6H4NH2 (0.043 g, 0.398 mmol) and dissolve the resulting precipitate via reflux for 12 h at 393 K. Cool the solution slowly to room temperature at a rate of 2 K h-1.\",Single crystal X-ray diffraction,Frames were collected using a Bruker SMART CCD area-detector diffractometer with Mo Ka radiation\r\n10.1107/S0108270106039746,\"bis(3,5-dimethylanilinium) lead iodide\",C16H24N2PbI4,\"bis¬≠(3,5-dimethyl¬≠anilinium) tetraiodoplumbate(II), (C6H3NH3(CH3)2)2PbI4\",C8H12N,\"PbI4, Lead iodide\",\"bis(3,5-dimethylanilinium) lead (II) iodide\",1,single crystal,,,,,,,,\"PbI2, HI, C8H9NH2\",Yellow plate-like crystals,\"Dissolve PbI2 (0.060 g, 0.130 mmol) in 47% HI (2 ml) in a round-bottomed flask. Add C8H9NH2 (0.040 g, 0.330 mmol) and dissolve the resulting precipitate via reflux for 12 h at 363 K. Cool the solution slowly to room temperature at a rate of 2 K h-1.\",Single crystal X-ray diffraction,Frames were collected using a Bruker SMART CCD area-detector diffractometer with Mo Ka radiation\r\n10.1107/S1600536806013973,\"Bis(propane-1,2-diammonium) lead iodide trihydrate\",C6H24N4PbI6 3H2O,\"Bis(propane-1,2-diaminium) hexabromoplumbate(II), trihydrate, [NH3CH2CH(NH3)CH3]2[PbI6]3H2O\",C3H12N2,\"PbI6, Lead iodide\",\"Bis(propane-1,2-diaminium) lead iodide trihydrate\",0,single crystal,,,,,,,,\"PbI2, HI, NH2CH2CH(NH2)CH3\",Colourless crystal,\"Dissolve PbI2 (0.220 g, 0.477 mmol) in 47% HI (3 ml) in a round-bottomed flask. Add NH2CH2CH(NH2)CH3 (0.200 g, 2.70 mmol), dissolve the resulting precipitate by refluxing for 12 h at 363 K. Slowly cool the solution to room temperature at 2 K/h.\",Single-crystal X-ray diffraction,Bruker SMART CCD area-detector diffractometer with Mo Kα radiation.\r\n10.1107/S160053680903712X,Bis(phenylethylammonium) lead bromide,C16H24N2PbBr4,\"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",C8H12N,\"PbBr4, Lead bromide\",bis(2-phenylethan-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,Not stated.,Crystals,\"Grown at room temperature from a solution in N,Ndimethylformamide (DMF) using nitromethane as the poor solvent.\",X-ray diffraction,Rigaku R-AXIS RAPID diffractometer with Mo K\u0003a radiation. Refer to the first page of the paper for details.\r\n10.1126/sciadv.1700704,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,unknown,Quantum Espresso,DFT,,6x6x1,,ultra-soft pseudopotentials,,,,,,\r\n10.1126/sciadv.aay0571,bismethylbenzylammonium lead iodide,C16H24N2PbI4,\"(MBA)2PbI4, Œ±-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",bismethylbenzylaminium lead (II) iodide,2,film,,,,,,,,\"DMF, lead oxide (PbO, 99.999%), (±)-α-methylbenzylamine (rac-MBA, 99%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",Thin film on quartz substrate,\"200 mg of PbO (0.897 mmol), 200 μl (1.57 mmol) of rac-MBA were dissolved in 6 ml of HI by heating at 90°C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1°C/hour. The obtained crystals were filtered and washed with diethyl ether.\r\nThe crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto quartz substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100°C for 10 min.\",UV-vis absorption,\r\n10.1126/sciadv.aay0571,bismethylbenzylammonium lead iodide,C16H24N2PbI4,\"(MBA)2PbI4, Œ±-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",bismethylbenzylaminium lead (II) iodide,2,film,,,,,,,,\"DMF, lead oxide (PbO, 99.999%), (R)-(+)-α-methylbenzylamine (R-MBA, 98%, ee 96%), (S)-(−)-α-methylbenzylamine (S-MBA, 98%, ee 98%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",Thin film on quartz substrate,\"200 mg of PbO (0.897 mmol), 200 μl (1.57 mmol) of R-, S-MBA were dissolved in 6 ml of HI by heating at 90°C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1°C/hour. The obtained crystals were filtered and washed with diethyl ether. The crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto quartz substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100°C for 10 min.\",Circular Dichroism (CD) Spectroscopy,A Jasco J-715 spectropolarimeter was used on thin film samples. Spectra were averaged over five scans. An internal algorithm in the Jasco software package was used to smooth the spectra. CD spectra were taken from 200 to 600 nm at 0.2-nm resolution.\r\n10.1126/sciadv.aay0571,bismethylbenzylammonium lead iodide,C16H24N2PbI4,\"(MBA)2PbI4, Œ±-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",bismethylbenzylaminium lead (II) iodide,2,film,,,,,,,,\"DMF, lead oxide (PbO, 99.999%), (R)-(+)-α-methylbenzylamine (R-MBA, 98%, ee 96%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",Thin film on ITO substrate,\"200 mg of PbO (0.897 mmol), 200 μl (1.57 mmol) of R-MBA were dissolved in 6 ml of HI by heating at 90°C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1°C/hour. The obtained crystals were filtered and washed with diethyl ether. The crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto ITO substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100°C for 10 min.\",Magnetic conductive-probe atomic force microscopy,\"A Veeco D5000 AFM system in an Ar-filled glovebox with a NanoScope V controller was used to perform the conductive atomic force microscopy. A Bruker MESP-V2 tip was used. The Co-Cr coated tips were pre-magnetized by a strong permanent magnet for 30 minutes and immediately following were used to scan. I-V curves were generated by increasing the bias voltage from -2 to +2 Volts, and a scan rate of 0.5 Hz in contact mode was used. More than 100 I-V curves were taken in different locations for each sample.\"\r\n10.1126/sciadv.aay0571,bismethylbenzylammonium lead iodide,C16H24N2PbI4,\"(MBA)2PbI4, Œ±-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",C8H12N,\"PbI4, Lead iodide\",bismethylbenzylaminium lead (II) iodide,2,film,,,,,,,,\"DMF, lead oxide (PbO, 99.999%), (S)-(−)-α-methylbenzylamine (S-MBA, 98%, ee 98%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",Thin film on ITO substrate,\"200 mg of PbO (0.897 mmol), 200 μl (1.57 mmol) of S-MBA were dissolved in 6 ml of HI by heating at 90°C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1°C/hour. The obtained crystals were filtered and washed with diethyl ether. The crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto ITO substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100°C for 10 min.\",Magnetic conductive-probe atomic force microscopy,\"A Veeco D5000 AFM system in an Ar-filled glovebox with a NanoScope V controller was used to perform the conductive atomic force microscopy. A Bruker MESP-V2 tip was used. The Co-Cr coated tips were pre-magnetized by a strong permanent magnet for 30 minutes and immediately following were used to scan. I-V curves were generated by increasing the bias voltage from -2 to +2 Volts, and a scan rate of 0.5 Hz in contact mode was used. More than 100 I-V curves were taken in different locations for each sample.\"\r\n10.1126/sciadv.aay4045,Bis(butylammonium) lead bromide,C8H24N2PbBr4,\"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",C4H12N,\"PbBr4, Lead bromide\",bis(butyl-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"BABr (synthesized), PbBr2, HBr\",Colorless single crystals,\"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",UV-vis absorption,A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2CsPb2Br7,\"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",C8H24N2,\"CsPb2Br7, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",UV-vis absorption,A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2Cs2Pb3Br10,\"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",C8H24N2,\"Cs2Pb3Br10, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",UV-vis absorption,A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) lead bromide,C8H24N2PbBr4,\"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",C4H12N,\"PbBr4, Lead bromide\",bis(butyl-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"BABr (synthesized), PbBr2, HBr\",Colorless single crystals,\"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",UV-vis absorption,A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2CsPb2Br7,\"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",C8H24N2,\"CsPb2Br7, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",UV-vis absorption,A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2Cs2Pb3Br10,\"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",C8H24N2,\"Cs2Pb3Br10, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",UV-vis absorption,A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) lead bromide,C8H24N2PbBr4,\"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",C4H12N,\"PbBr4, Lead bromide\",bis(butyl-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"BABr (synthesized), PbBr2, HBr\",Colorless single crystals,\"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Photoluminescence microscopy,PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2CsPb2Br7,\"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",C8H24N2,\"CsPb2Br7, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Photoluminescence microscopy,PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2Cs2Pb3Br10,\"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",C8H24N2,\"Cs2Pb3Br10, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Photoluminescence microscopy,PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) lead bromide,C8H24N2PbBr4,\"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",C4H12N,\"PbBr4, Lead bromide\",bis(butyl-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"BABr (synthesized), PbBr2, HBr\",Colorless single crystals,\"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Photoluminescence microscopy,PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2CsPb2Br7,\"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",C8H24N2,\"CsPb2Br7, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Photoluminescence microscopy,PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2Cs2Pb3Br10,\"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",C8H24N2,\"Cs2Pb3Br10, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr, CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2Csn-1PbBr3n+1 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution in an appropriate stoichiometry. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling to room temperature colorless (n = 1) and yellow (n = 2 and 3) precipitated in their respective solutions. The crystals were removed by suctio9n filtration and were dried in a vacuum. Pure-phase single crystals were obtained via the following BA:Cs:Pb ratios: n = 1, 2:0:1; n = 2, 3:1:2, n = 3, 3.5:2:3.\",Photoluminescence Spectra,A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used to measure low-temperature PL. An excitation wavelength of 375 nm was used. PL spectra at high temperature was performed in the same system with a HCP422G gas-tight hot plate.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) lead bromide,C8H24N2PbBr4,\"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",C4H12N,\"PbBr4, Lead bromide\",bis(butyl-1-aminium) lead(II) bromide,2,single crystal,,,,,,,,\"BABr (synthesized), PbBr2, HBr\",Colorless single crystals,\"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Single-crystal X-ray diffraction,A synchrotron radiation source ( λ = 0.7749 Å) in a nitrogen atmosphere was used for the SCXRD data. The crystals were mounted on a Bruker diffractometer using a Kapton tip. Nitrogen cryogen with a temperature controller precisely adjusted the temperature during measurement. APEX 3 software was used for data reduction and SADABS software was used for multiscan absorption correction. Structure calculations were performed using the SHELXTL program.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2Cs2Pb3Br10,\"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",C8H24N2,\"Cs2Pb3Br10, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Single-crystal X-ray diffraction,A synchrotron radiation source ( λ = 0.7749 Å) in a nitrogen atmosphere was used for the SCXRD data.  The crystals were mounted on a Bruker diffractometer with a Kapton tip. Nitrogen cryogen with a temperature controller precisely adjusted the temperature during measurement. APEX 3 software was used for data reduction and SADABS software was used for multiscan absorption correction. Structure calculations were performed using the SHELXTL program.\r\n10.1126/sciadv.aay4045,Bis(butylammonium) caesium lead bromide,C8H24N2CsPb2Br7,\"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",C8H24N2,\"CsPb2Br7, Caesium lead bromide\",bis(butane-1-aminium) caesium lead bromide,2,single crystal,,,,,,,,\"BABr (synthesized), CsBr, PbBr2, HBr\",Yellow single crystals,\"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100°C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20°C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",Single-crystal X-ray diffraction,A synchrotron radiation source ( λ = 0.7749 Å) in a nitrogen atmosphere was used for the SCXRD data. The crystals were mounted on a Bruker diffractometer using a Kapton tip. Nitrogen cryogen with a temperature controller precisely adjusted the temperature during measurement. APEX 3 software was used for data reduction and SADABS software was used for multiscan absorption correction. Structure calculations were performed using the SHELXTL program.\r\n10.1126/sciadv.abq4524,Tributyl(methyl)phosphonium lead iodide,C13H30PPbI3,\"tributyl(methyl)phosphonium lead iodide, TPPbI3\",C13H30P,\"PbI3, lead iodide\",,1,film,,,,,,,,\"TPI, PbI2, dimethylformamide (DMF)\",Tributyl(methyl)phosphonium lead iodide film,\"PbI2 (0.5 mol) and TPI (0.5 mol) were both dissolved in DMF (1 mL). The resulting solution (30 μL) was dropped onto a glass surface. Spin-coating was performed at 5000 rpm for 30 seconds, then the film was annealed at 100°C for 5 minutes.\",UV-Vis Spectroscopy,\"The absorbance spectrum of TPPbI3 films were recorded using UV-Vis spectroscopy, no information about equipment given.\"\r\n10.1126/sciadv.abq4524,Tributyl(methyl)phosphonium lead iodide,C13H30PPbI3,\"tributyl(methyl)phosphonium lead iodide, TPPbI3\",C13H30P,\"PbI3, lead iodide\",,1,film,,,,,,,,\"TPI, PbI2, dimethylformamide (DMF)\",Tributyl(methyl)phosphonium lead iodide film,\"PbI2 (0.5 mol) and TPI (0.5 mol) were both dissolved in DMF (1 mL). The resulting solution (30 μL) was dropped onto a glass surface. Spin-coating was performed at 5000 rpm for 30 seconds, then the film was annealed at 100°C for 5 minutes.\",UV-Vis Spectroscopy,\"The absorbance spectrum of TPPbI3 films were recorded using UV-Vis spectroscopy, no information about equipment given.\r\nThe band gap was determined from the absorption spectrum.\"\r\n10.1126/science.267.5203.1473,Diiodoformamidinium bis(methylammonium) tin iodide,C4H20I2N5Sn2I8,\"diiododiaminomethanide bis(methanaminium) bis(tetraiodostannate(II)), [NH2C(I)=NH2]2(CH3NH3)2Sn2I8\",\"CH4IN2, CH6N\",\"Sn2I8, Tin iodide\",diiododiaminomethanide bis(methanaminium),2,single crystal,,,,,,,,\"CH3NH2•Hl, NH2CN, Snl2, HI\",Crystals,\"CH3NH2•Hl (2.772 g, 17.44 mmol), NH2CN (0.733 g, 17.44 mmol), and Snl2 (6.495 g, 17.44 mmol) were dissolved in 70 ml of 57 weight % aqueous HI solution at 80°C. After soaking at 80°C for 12 hours, the solution was cooled to -10°C at 2°C/hour. The product was filtered under nitrogen, dried in flowing argon at 80°C for several hours, and then removed to an argon-filled dry box with oxygen and water levels maintained at <1 part per million.\",Single crystal X-ray diffraction,Enraf-Nonius CAD4 single-crystal diffractometer and graphite monochromatized MoKa radiation.\r\n10.1126/science.267.5203.1473,Diiodoformamidinium tris(methylammonium) tin iodide,C5H26I2N7Sn3I11,\"diiododiaminomethanide tris(methanaminium) tris(tetraiodostannate(II)), [NH2C(I)=NH2]2(CH3NH3)3Sn3I11\",\"CH4IN2, CH6N\",\"Sn3I11, Tin iodide\",diiododiaminomethanide tris(methanaminium),2,single crystal,,,,,,,,\"CH3NH2•Hl, NH2CN, Snl2, HI\",Sheet-like crystals,\"Prepare a 2:5:5 molar ratio of NH2CN, CH3NH2•HI, and Snl2 dissolved in 70 ml of 57 weight % aqueous HI solution at 80°C. After soaking at 80°C for 12 hours, the solution was cooled to -10°C at 2°C/hour. The product was filtered under nitrogen, dried in flowing argon at 80°C for several hours, and then removed to an argon-filled dry box with oxygen and water levels maintained at <1 part per million. The product contained a mixture of [NH2C(I)=NH2]2(CH3NH3)3Sn3I11 and CH3NH2Snl3. The sheet-like [NH2C(I)=NH2]2(CH3NH3)3Sn3I11 crystals could be mechanically separated from the rod-like or rhombic dodecahedral cubic perovskite crystals because of the very different crystalline habit for these two materials.\",Single crystal X-ray diffraction,Enraf-Nonius CAD4 single-crystal diffractometer and graphite monochromatized MoKa radiation.\r\n10.1126/science.267.5203.1473,Diiodoformamidinium tetrakis(methylammonium) tin iodide,C6H32I2N8Sn4I14,\"[NH2C(I)=NH2]2(CH3NH3)4Sn4I14, diiododiaminomethanide tetrakis(methanaminium) tetradecaiodo tetrastannate(II)\",\"CH4IN2, CH6N\",\"Sn4I14, Tin iodide\",diiododiaminomethanide tetrakis(methanaminium),2,single crystal,,,,,,,,\"CH3NH2•Hl, NH2CN, Snl2, HI\",Sheet-like crystals,\"Add large excess of CH3NH2•HI and Snl2 to NH2CN dissolved in 70 ml of 57 weight % aqueous HI solution at 80°C. After soaking at 80°C for 12 hours, the solution was cooled to -10°C at 2°C/hour. The product was filtered under nitrogen, dried in flowing argon at 80°C for several hours, and then removed to an argon-filled dry box with oxygen and water levels maintained at <1 part per million. The [NH2C(I)=NH2]2(CH3NH3)4Sn4I14 crystals could be mechanically separated from the rod-like or rhombic dodecahedral cubic perovskite crystals because of the very different crystalline habit for these two materials.\",Single crystal X-ray diffraction,Enraf-Nonius CAD4 single-crystal diffractometer and graphite monochromatized MoKa radiation.\r\n10.1126/science.aai8535,Trimethylchloromethylammonium manganese chloride,(Me3NCH2Cl)MnCl3,\"trimethylchloro-methanaminium trichloromanganate(II), TMCM-MnCl3\",C4NH11Cl,\"MnCl3, manganese chloride\",trimethylchloro-methanaminium manganese chloride,1,unknown,,,,,,,,\"Trimethylamine (30 wt % in water) and dichloromethane, acetonitrile, manganese(II) chloride (MnCl2)\",red block-shaped Me3NCH2ClMnCl3 (TMCM-MnCl3) crystals,\"Equimolar amounts of Trimethylamine (30 wt% in water) and dichloromethane were mixed in acetonitrile and kept at room temperature for 24 hours. The obtained colorless solid ((Chloromethyl)trimethylammonium chloride) was collected.\r\nThe (Chloromethyl)trimethylammonium chloride (50 mmol) was then mixed with anhydrous MnCl2 (50 mmol) in 100 ml of methanol. Crystals were obtained by a slow evaporation. Film was then made by spin coating the solution on an ITO-glass substrate.\",UV-vis absorption,\r\n10.1126/science.aai8535,Trimethylchloromethylammonium manganese chloride,(Me3NCH2Cl)MnCl3,\"trimethylchloro-methanaminium trichloromanganate(II), TMCM-MnCl3\",C4NH11Cl,\"MnCl3, manganese chloride\",trimethylchloro-methanaminium manganese chloride,1,powder,,,,,,,,\"Trimethylamine (30 wt % in water) and dichloromethane, acetonitrile, manganese(II) chloride (MnCl2)\",red block-shaped Me3NCH2ClMnCl3 (TMCM-MnCl3) crystals,Equimolar amounts of Trimethylamine (30 wt% in water) and dichloromethane was mixed in acetonitrile at room temperature for 24 hours. The (Chloromethyl)trimethylammonium chloride (50 mmol) was then mixed with anhydrous manganese(II) (50 mmol) in 100 ml of methanol.,Photoluminescence,\r\n10.1139/v90-063,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,single crystal,,,,,,,,\"HBr, CH3NH2, Pb(NO3)2\",MAPbBr3 Single-crystal,Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH3Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Yield: 9.5 g.,X-ray diffraction,\"CAD-4 four-circle diffractometer; Mo Kα, λ = 0.70926 Å (graphite monochromator); T = 18 °C. Lorentz, polarization, and absorption corrections applied. Refer to page 413 Experimental.\"\r\n10.1139/v90-063,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,single crystal,,,,,,,,\"HCl, CH3NH2, PbCl2\",MAPbCl3 Single-crystal,Primarily referenced the methods of [1] and [2]. The synthesis of MAPbBr3 in ref [2] was modified to prepare MAPbCl3.,Single crystal X-ray diffraction,\"CAD-4 four-circle diffractometer; Mo Kα, λ = 0.70926 Å (graphite monochromator); T = 18 °C. Lorentz, polarization, and absorption corrections applied. Refer to page 413 Experimental.\"\r\n10.1139/v90-063,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"HI, CH3NH2, Pb(NO3)2\",MAPbI3 Powder,Add concentrated HI to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH2I solution. Organic crystals form while dripping in the solution. Cool the solution to not below 40°C and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum.,X-ray diffraction,\"Diffraction pattern of some of the lines corresponding to Weber's cubic (a = 6.27 A) were split up or broadened, indicating that MAPbI3 at room temperature is not strictly cubic. Refer to page 413 Experimental.\"\r\n10.1139/v90-063,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"HBr, CH3NH2, Pb(NO3)2\",Partially deuterated MAPbBr3,Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH2Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Partially N-deuterated samples required for the NMR studies were prepared using D-containing solutions. Refer to Page 413 Experimental.,2H and 14N NMR,\"Measurements were carried out at 8.48 T with a Nicolet 360NB spectrometer using a broad band (16-58 MHz) variable-temperature 10 mm probe supplied by Nicolet. The 2-H and 14-N frequencies were 55.427 and 26.083 MHz, respectively. Refer to Page 414 Results section Existence of transitions subsection.\"\r\n10.1139/v90-063,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"HCl, CD3NH2, PbCl2\",CD3NH3PbCl3 crystals,Primarily referenced the methods of [1] and [2]. The synthesis of MAPbBr3 in ref [2] was modified to prepare CD3NH3PbCl3.,2H and 14N NMR,\"Measurements were carried out at 8.48 T with a Nicolet 360NB spectrometer using a broad band (16-58 MHz) variable-temperature 10 mm probe supplied by Nicolet. The 2-H and 14-N frequencies were 55.427 and 26.083 MHz, respectively. Refer to Page 414 Results section Existence of transitions subsection.\"\r\n10.1139/v90-063,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,powder,,,,,,,,\"HI, CH3NH2, Pb(NO3)2\",Partially deuterated MAPbI3,Add concentrated HI to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH2I solution. Organic crystals form while dripping in the solution. Cool the solution to not below 40°C and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Partially N-deuterated samples required for the NMR studies were prepared using D-containing solutions. Refer to Page 413 Experimental.,2H and 14N NMR,\"Measurements were carried out at 8.48 T with a Nicolet 360NB spectrometer using a broad band (16-58 MHz) variable-temperature 10 mm probe supplied by Nicolet. The 2-H and 14-N frequencies were 55.427 and 26.083 MHz, respectively. Refer to Page 414 Results section Existence of transitions subsection.\"\r\n10.1139/v90-063,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,\"HBr, CH3NH2, Pb(NO3)2\",MAPbBr3 Single-crystal,Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100°C to the concentrated CH3NH3Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Yield: 9.5 g.,Adiabatic calorimetry,\"The heat capacities were measured in an adiabatic calorimeter from 30 to 300 K, using sample masses of 12.8235 g MAPbBr3. Refer to Page 414 Table 1.\"\r\n10.1139/v90-063,Methylammonium lead chloride,CH6NPbCl3,\"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",CH6N,\"PbCl3, Lead chloride\",methanaminium lead (II) chloride,3,powder,,,,,,,,\"HCl, CH3NH2, PbCl2\",MAPbCl3 Single-crystal,Primarily referenced the methods of [1] and [2]. The synthesis of MAPbBr3 in ref [2] was modified to prepare MAPbCl3.,Adiabatic calorimetry,\"The heat capacities were measured in an adiabatic calorimeter from 30 to 345 K, using sample masses of 14.6883 g MAPbCl3. Refer to Page 414 Table 1.\"\r\n10.1143/JPSJ.71.1694,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"CH3NH3PbI3, lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",Black and opaque MAPbI3 Single crystal,CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ (by adding a 40% solution of CH3NH2 in water) dissolved in concentrated HI solution. Cool aqueous solution from l00°C to not lower than 40°C to obtain a black crystal. Crystals of about 1 cm in dimension were obtained. Synthesis using reference [2].,Single crystal X-ray diffraction,\"Spherical samples were cut and polished into 0.3mm in diameter, among which a single crystal was selected and was mounted on an off-centered 4-circle diffractometer (HUBER 424) controlled by MXC (Mac Science). Graphite-monochromated Mo K\\alpha radiation was used from a rotating anode generator with 50 kV–250 mA. Refer to Page 1695 Table I (Params); Page 1696 Table II (Apos).\"\r\n10.1143/JPSJ.71.1694,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"CH3NH3PbI3, lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",Black and opaque MAPbI3 single crystal,CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ (by adding a 40% solution of CH3NH2 in water) dissolved in concentrated HI solution. Cool aqueous solution from l00°C to not lower than 40°C to obtain a black crystal. Crystals of about 1 cm in dimension were obtained. Synthesis using reference [2],X-ray diffraction,Cut and polish samples into 0.3mm in diameter. Select a single crystal and mount on an off-centered 4-circle diffractometer (HUBER 424) controlled by MXC (Mac Science). Use cold nitrogen gas flow (Oxford Crysteram) to keep the temperature of the sample within ±0.5 K. Use graphite-monochromated Mo-K\\alpha radiation from a rotating anode generator with 50 kV–250 mA. Refer to Page 1695 Fig. 1.\r\n10.1515/ncrs-1999-0318,Bis(phenylmethylammonium) lead chloride,C14H20N2PbCl4,\"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",C7H10N,\"PbCl4, Lead chloride\",bis(phenylmethanaminium) lead(II) chloride,2,single crystal,,,,,,,,\"Lead chloride, benzylamine (Merck), HCl, DMF\",Colorless crystals,\"Benzyl ammonium chloride was prepared by adding a stoichiometric amount of 37% concentrated HCl to benzylamine. Then, the solvent from a dimethylformamide solution of lead chloride and benzyl ammonium chloride (1:2) was slowly evaporated.\",Single crystal X-ray diffraction,\"Nicolet P3, Wyckoff diffractometer with Mo Ka radiation (0.71073 À)\"\r\n10.1515/ncrs-1999-0319,Bis(1-(2-naphthyl)methylammonium) lead chloride,C22H24N2PbCl4,\"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",C11H12N,\"PbCl4, Lead chloride\",1-(2-naphthyl)methylaminium lead(II) chloride,2,single crystal,,,,,,,,\"Lead chloride, 2-naphthylmethyl-amine, HCl, DMF\",Colorless crystals,\"Slowly evaporate the solvent from a solution of lead chloride and 2-naphthylmethyl-ammonium chloride with the ratio 1:2 in dimethylformamide.\r\n\r\nPrepare 2-naphthylmethyl-amine (NMA) according to the procedure outlined in [1] and [2]. Add a stoichiometric amount of 37% concentrated HCl to prepare the adjunct hydrochloride salt.\",X-ray diffraction,\"Nicolet P3, Wyckoff diffractometer with Mo Ka radiation (0.71073 Â)\"\r\n10.1515/ncrs-1999-0320,Bis(2-anthrylmethylammonium) lead chloride,C30H28N2PbCl4,\"bis(anthracen-1-ylmethanaminium) tetrachloroplumbate(II), AMA2PbCl4, (C15H11NH3)2PbCl4, (C15H14N)2PbCl4\",C15H14N,\"PbCl4, Lead chloride\",bis(anthracen-1-ylmethanaminium) lead(II) chloride,2,single crystal,,,,,,,,\"Lead chloride, 2-anthrylmethyl-amine, HCl, DMF\",Colorless crystals,\"Prepare 2-anthrylmethyl-amine from the procedure outlined in [1] and [2]. Prepare the adjunct hydrochloride salt by adding a stoichiometric amount of 37% concentrated HCl.\r\n\r\nSlowly evaporate the solvent from a solution of lead chloride and 2-anthrylmethyl-ammonium chloride with the stoichiometric 1:2 in dimethylformamide.\",X-ray diffraction,\"Nicolet P3, Wyckoff with Mo Ka radiation (0.71073 Â). Programs used were SHELXS-86 and SHELXL-93.\"\r\n10.1515/znb-1993-0727,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,bulk polycrystalline,,,,,,,,phenyl ethyl ammonium iodide (C6H5CH2CH2NH3I) and tin iodide (SnI2),brown-golden plate-like (C6H5CH2CH2NH3)2SnI4 crystals,\"In an argon atmosphere, 540 mg (2.16 mmol) of C6H5CH2CH2NH3I was mixed with 373 mg (1 mmol) of SnI2 in 10 ml of acetonitrile under stirring. 4 ml of the solvent was evaporated by heating at 75 degrees C. The solution was then cooled to 10 degrees C. Finally, the precipitate was filtered and dried at 40 degrees celsius.\",UV-vis absorption,The spectrum was recorded on Varian model 2390 spectrophotometer\r\n10.1515/znb-1993-0727,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,bulk polycrystalline,,,,,,,,phenyl ethyl ammonium iodide (C6H5CH2CH2NH3I) and tin iodide (SnI2),brown-golden plate-like (C6H5CH2CH2NH3)2SnI4 crystals,\"In an argon atmosphere, 540 mg (2.16 mmol) of C6H5CH2CH2NH3I was mixed with 373 mg (1 mmol) of SnI2 in 10 ml of acetonitrile under stirring. 4 ml of the solvent was evaporated by heating at 75 degrees C. The solution was then cooled to 10 degrees C. Finally, the precipitate was filtered and dried at 40 degrees celsius.\",Photoluminescence,\"The spectrum was recorded using Jobin-Yvon model HG2S Raman spectrophoto­meter, using an argon laser.\"\r\n10.1515/znb-1999-1112,Bis(phenylmethylammonium) lead iodide,C14H20N2PbI4,\"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",C7H10N,\"PbI4, Lead iodide\",bis(phenylmethanaminium) lead(II) iodide,2,single crystal,,,,,,,,\"PbI2 (Johnson Matthey, 976204), PbO (Ferak 01-881), hydroiodic acid 57% (Merck 341), H3PO2 50% (Fluka 9421), benzylamine (Fluka 13180)\",Orange plate crystals,\"To prepare C6H5CH2NH3I, treat benzylamine with aq.HI 57% in the presence of H3PO2 and recrystallize the precipitate from acetonitrile.\r\n\r\nTreat C6H5CH2NH3I and PbI2 in molar ratio 2:1 in CH3CN or DMF to obtain small crystals. \r\n\r\nDissolve C6H5CH2NH2 (107 mg, 1 mmol) and PbO (111.5 mg, 0.5 mmol) in aq. HI (57%) in the presence of H3PO2 at reflux temperature to obtain large crystals. \r\n\r\nSlowly cool the solution and obtain the crystals several hours later, filter and dry in air.\",X-ray diffraction,Collect on a Crystal Logic dual goniometer using graphite monochromated MoKa radiation. Unit cell dimensions were determined and refined by using the angular setting of 24 automatically centered reflections in the range 11° < 29 < 24°. Intensity data were recorded using a Theta-2theta scan. Refer to page 1406 for details.\r\n10.2138/am-2002-8-917,Calcium titanate,CaTiO3,\"Perovskite, Calcium dioxido(oxo)titanium, Calcium titanate, CaTiO3\",None,CaTiO3,,3,single crystal,,,,,,,,\"CaTiO3 powder, TiO2\",crystals with a maximum size of 1000 • 400 • 500 mm,Powder of CaTiO3 was heated with TiO2 flux at 1650 deg C for 24 hours. The temperature was gradually decreased by 5 deg C/hour to 1500 deg C.,Single crystal X-ray diffraction,\"A four-circle diffractometer (RIGAKU AFC-5 and AFC-6) using MoKa radiation (l = 0.71069 Å) emitted from a rotating anode X-ray generator (50 kV, 180 mA) with a graphite monochromator was used.\"\r\nDOI 10.1007/s12274-015-0948-y,tris(methylammonium) bismuth iodide,C3H18N3Bi2I9,\"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",CH6N,\"Bi2I9, Bismuth iodide\",tris(methanaminium) bismuth iodide,0,film,,,,,,,,\"methylammonium iodide (MAI), bismuth iodide (BiI3), DMF (N,N-dimethylformamide), FTO covered with TiO2 mesoporous layers\",Red ~500 nm thick film,\"0.2384 g of MAI and 0.5897 g of BiI3 were mixed in 1 mL of DMF. The solution was filtered using PTFE syringe filters (0.45 μm) before use. 50 μL of the solution was spin-coated at 4,000 rpm for 30 s with a ramp rate of 4,000 rpm·s–1. The film was heated at 100 °C for 10 min on a hotplate.\",UV–vis absorption (reflectance),The absorption spectrum was recorded using Shimadzu UV2450. The band gap value was obtained by Tauc plot with an indirect band gap assumption.\r\ndoi.org/10.1021/acs.inorgchem.7b02285,\"N,N-dimethylphenylene-p-diammonium lead iodide\",C8H14N2PbI4,\"benzene-1,4-di(methanaminium) tetraiodoplumbate(II)\",C8H14N2,\"PbI4, Lead iodide\",\"benzene-1,4-di(methanaminium) lead (II) iodide\",2,single crystal,,,,,,,,\"Pb(CH3COO)2·3H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HI (57 wt % in H2O, stabilized with H3PO4, 99.95%), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",Red block-like crystal,\"Pb(CH3COO)2·3H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HI and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at −70 °C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 × 10 mL). The precipitate was redissolved in 5 mL of HI and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",Single crystal XRD,a Bruker Quazar SMART APEXII diffractometer with Mo Kα (λ = 0.71073 Å) radiation was used to collect the data.\r\ndoi.org/10.1021/acs.inorgchem.7b02285,\"N,N-dimethylphenylene-p-diammonium lead bromide\",C8H14N2PbBr4,\"benzene-1,4-di(methanaminium) tetrabromoplumbate(II)\",C8H14N2,\"PbBr4, Lead bromide\",\"benzene-1,4-di(methanaminium) lead (II) bromide\",2,single crystal,,,,,,,,\"Pb(CH3COO)2·3H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HBr (48 wt % in H2O), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",Yellow block-like crystal,\"Pb(CH3COO)2·3H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HBr and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at −70 °C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 × 10 mL). The precipitate was redissolved in 5 mL of HBr and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",Single crystal X-ray diffraction,a Bruker Quazar SMART APEXII diffractometer with Mo Kα (λ = 0.71073 Å) radiation was used to collect the data.\r\ndoi.org/10.1021/acs.inorgchem.7b02285,\"N,N-dimethylphenylene-p-diammonium lead iodide\",C8H14N2PbI4,\"benzene-1,4-di(methanaminium) tetraiodoplumbate(II)\",C8H14N2,\"PbI4, Lead iodide\",\"benzene-1,4-di(methanaminium) lead (II) iodide\",2,single crystal,,,,,,,,\"Pb(CH3COO)2·3H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HI (57 wt % in H2O, stabilized with H3PO4, 99.95%), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",Red block-like crystal,\"Pb(CH3COO)2·3H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HI and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at −70 °C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 × 10 mL). The precipitate was redissolved in 5 mL of HI and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",Single crystal X-ray diffraction,a Bruker Quazar SMART APEXII diffractometer with Mo Kα (λ = 0.71073 Å) radiation was used to collect the data.\r\ndoi.org/10.1021/acs.inorgchem.7b02285,\"N,N-dimethylphenylene-p-diammonium lead bromide\",C8H14N2PbBr4,\"benzene-1,4-di(methanaminium) tetrabromoplumbate(II)\",C8H14N2,\"PbBr4, Lead bromide\",\"benzene-1,4-di(methanaminium) lead (II) bromide\",2,single crystal,,,,,,,,\"Pb(CH3COO)2·3H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HBr (48 wt % in H2O), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",Yellow block-like crystal,\"Pb(CH3COO)2·3H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HBr and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at −70 °C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 × 10 mL). The precipitate was redissolved in 5 mL of HBr and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",Single crystal X-ray diffraction,a Bruker Quazar SMART APEXII diffractometer with Mo Kα (λ = 0.71073 Å) radiation was used to collect the data.\r\ndoi.org/10.1021/acsmaterialslett.9b00102,Phenethylammonium perfluorophenethylammonium lead iodide,C32H38N4F2Pb2I8,\"phenethanaminium perfluorophenethanaminium octaiodo diplumbate(II)), ((PEA)0.5(F[5]-PEA)0.5)2PbI4\",\"C8H12N, F5C8H7N\",\"Pb2I8, Lead iodide\",phenethanaminium perfluorophenethanaminium lead (II) iodide,2,single crystal,,,,,,,,\"n-Butanol, 57wt% stabilized HI (Alfa Aesar), perfluorophenethylammonium iodide (F5-PEAI; synthesized), phenethylammonium iodide (PEAI; synthesized)\",Yellow plate-like crystals,\"In 0.5 ml n-Butanol and 0.1 ml 57wt% stabilized HI, 69.2 mg PbI2, 50.9 mg F5-PEAI and 37.4 mg PEAI were dissolved at 95 °C. The solution was slowly cooled down at 1 °C/h to room temperature and the solids were collected.\",Single crystal X-ray Diffraction,Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo K radiation source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\r\ndoi.org/10.1021/acsmaterialslett.9b00102,Bis(perfluorophenethylammonium) lead iodide,C32H38F2N4Pb2I8,\"bis(2-(perfluorophenyl)ethan-1-aminium) octoiodo diplumbate(II), (F[5]-PEA)2PbI4\",C8H7F5N,\"Pb2I8, Lead iodide\",bis(2-(perfluorophenyl)ethan-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"n-Butanol, 57wt% stabilized HI (Alfa Aesar), perfluorophenethylammonium iodide (F5-PEAI; synthesized)\",Yellow plate-like crystals,\"In 0.5 ml n-Butanol and 0.1 ml 57wt% stabilized HI, 69.2 mg PbI2 and 101.7 mg F5-PEAI were dissolved  at 95 °C. The solution was slowly cooled down at 1 °C/h to room temperature and the solids were collected.\",Single crystal X-ray Diffraction,Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo K radiation source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\r\ndoi.org/10.1021/acsmaterialslett.9b00102,Bis(perfluorophenethylammonium) lead iodide,C32H38F2N4Pb2I8,\"bis(2-(perfluorophenyl)ethan-1-aminium) octoiodo diplumbate(II), (F[5]-PEA)2PbI4\",C8H7F5N,\"Pb2I8, Lead iodide\",bis(2-(perfluorophenyl)ethan-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,,,,,\r\ndoi.org/10.1021/jacs.1c08514,Bis(ethanolammonium) lead iodide,C4H16N2O2PbI4,\"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",OC2NH8,\"PbI4, Lead iodide\",,2,powder,,,,,,,,\"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",Red single crystals (EOA2PbI4),\"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 μL, 1.3 mmol) is added. This solution is sonicated at room temperature for five minutes. It is then kept at 3 °C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",Diffuse reflectance spectroscopy,Powder samples of EOA2PbI4 were used to measure absorption. Linear absorptions can be determined from measurements of UV-vis reflection.\r\ndoi.org/10.1021/jacs.1c08514,Bis(ethanolammonium) lead iodide,C4H16N2O2PbI4,\"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",OC2NH8,\"PbI4, Lead iodide\",,2,single crystal,,,,,,,,\"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",Red single crystals (EOA2PbI4),\"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 μL, 1.3 mmol) is added. This solution is sonicated at room temperature  for five minutes. It is then kept at 3 °C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",Pump-probe spectroscopy,\"Pump-probe delay spectroscopy was used with single crystals of EOA2PbI4 to measure transient reflectance spectra. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration ∼60 fs, ∼5 mJ/pulse, and 1 kHz repetition rate) was used for this measurement, and a Helios Ultrafast System was used as the transient reflection spectrometer. A fundamental beam of 800 nm was split into two beams, one being sent to generate the pump pulse and the other focused to create the white light probe (1.6---2.8 eV). The pump beam size was ∼590 μm and the probe size was ∼200 μm. The pump beam was sent directly toward the crystal from 90°, and the probe beam hit the crystal at 45°.\"\r\ndoi.org/10.1021/jacs.1c08514,Bis(ethanolammonium) lead iodide,C4H16N2O2PbI4,\"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",OC2NH8,\"PbI4, Lead iodide\",,2,single crystal,,,,,,,,\"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",Red single crystals (EOA2PbI4),\"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 μL, 1.3 mmol) is added. This solution is sonicated at room temperature  for five minutes. It is then kept at 3 °C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",Pump-probe spectroscopy,\"Pump-probe delay spectroscopy was used with single crystals of EOA2PbI4 to measure transient reflectance spectra. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration ∼60 fs, ∼5 mJ/pulse, and 1 kHz repetition rate) was used for this measurement, and a Helios Ultrafast System was used as the transient reflection spectrometer. A fundamental beam of 800 nm was split into two beams, one being sent to generate the pump pulse and the other focused to create the white light probe (1.6---2.8 eV). The pump beam size was ∼590 μm and the probe size was ∼200 μm. The pump beam was sent directly toward the crystal from 90°, and the probe beam hit the crystal at 45°. A Kramers---Kronig transformation was used to obtain the change in absorbance of the reflected light.\"\r\ndoi.org/10.1021/jacs.1c08514,Bis(3-iodopropylammonium) lead iodide,C6H18N2PbI6,\"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",C3H9NI,\"PbI4, Lead iodide\",bis(3-iodopropylaminium) lead (II) iodide,2,powder,,,,,,,,,,,,\r\ndoi.org/10.1021/jacs.1c08514,Bis(ethanolammonium) lead iodide,C4H16N2O2PbI4,\"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",OC2NH8,\"PbI4, Lead iodide\",,2,powder,,,,,,,,\"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",Red single crystals (EOA2PbI4),\"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 μL, 1.3 mmol) is added. This solution is sonicated at room temperature for five minutes. It is then kept at 3 °C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",Diffuse reflectance spectroscopy,\"Powder samples of EOA2PbI4 were used to measure absorption. Linear absorptions can be determined from measurements of UV-vis reflection, and a 2D Elliot formula was used to create a fit for the data. This formula can be found in the supporting information of the referenced publication and the files attached to this dataset. The formula can extract the exciton binding energy of this material. The analysis yields an exciton binding energy of ≈ 46 meV.\"\r\ndoi.org/10.1021/jacs.1c08514,Bis(3-iodopropylammonium) lead iodide,C6H18N2PbI6,\"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",C3H9NI,\"PbI4, Lead iodide\",bis(3-iodopropylaminium) lead (II) iodide,2,powder,,,,,,,,,,,,\r\ndoi.org/10.1021/jacs.1c08514,Bis(4-iodobutylammonium) lead iodide,C8H22N2PbI6,\"(I(CH2)4NH3)2PbI4, bis(4-iodobutylaminium) tetraiodoplumbate(II)\",C4H11NI,\"PbI4, Lead iodide\",bis(4-iodobutylaminium) lead (II) iodide,2,powder,,,,,,,,\"PbI2, HI(47%), butanolamine (HOC4H8NH2), ethyl acetate\",Yellow crystals of bis(4-iodobutylammonium) lead iodide,PbI2 (0.178 mmol; 0.082 g) was dissolved in 1 mL HI solution. Then HOC4H8NH2 (0.449 mmol; 0.040 g) was added. The precipitate was dissolved at 3 mL ethyl acetate and was kept undisturbed at room temperature. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom.,Reflectance spectroscopy,\"Powder samples of BIA2PbI4 were tested for absorption. Linear absorption was determined through UV-vis reflection. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration about 60 fs, about 5 mJ/pulse) was used to test the powder sample.\"\r\ndoi.org/10.1021/jacs.1c08514,Bis(4-iodobutylammonium) lead iodide,C8H22N2PbI6,\"(I(CH2)4NH3)2PbI4, bis(4-iodobutylaminium) tetraiodoplumbate(II)\",C4H11NI,\"PbI4, Lead iodide\",bis(4-iodobutylaminium) lead (II) iodide,2,powder,,,,,,,,\"PbI2, HI(47%), butanolamine (HOC4H8NH2), ethyl acetate\",Yellow crystals of bis(4-iodobutylammonium) lead iodide,PbI2 (0.178 mmol; 0.082 g) was dissolved in 1 mL HI solution. Then HOC4H8NH2 (0.449 mmol; 0.040 g) was added. The precipitate was dissolved at 3 mL ethyl acetate and was kept undisturbed at room temperature. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom.,Reflectance spectroscopy,\"Powder samples of BIA2PbI4 were tested for absorption. Linear absorption was determined through UV-vis reflection. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration about 60 fs, about 5 mJ/pulse) was used to test the powder sample.\"\r\ndoi.org/10.1021/jacs.9b11809,Bis(benzylammonium) lead iodide,C14H20N2PbI4,\"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",C7H10N,\"PbI4, lead iodide\",bis(benzylaminium) lead (II) iodide,2,single crystal,,,,,,,,\"Benzylamine (BzA), PbI2, Aq. HI (57%), H3PO2 (50 %)\",Orange (BzA)2PbI4 crystals,\"BzA (214.45 mg) was dissolved in Aq.HI (4.5 ml) treated with hypophosphorous acid (0.5 ml) as a stabilizer. A stoichiometric amount of PbI2 (461.01) was added to the above solution, stirred at 90 °C for 2 h, and cooled to room temperature at a rate of 1 K/hr to induce crystallization. All synthesis was performed at ambient conditions. The as-formed crystals were collected by suction, washed with diethyl ether and dried under vacuum.\",single crystal X-ray diffraction,\"Single crystal X-ray data were collected on a Nonius Kappa CCD single-crystal diffractometer (MoKα, λ = 0.71073 Å) at 180 K.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~17.3 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~7.9 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~7.4 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~6.9 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~6.2 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~5.4 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~4.9 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~17.3 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~7.9 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~7.4 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~6.9 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~6.2 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~5.4 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\ndoi.org/10.1038/s41563-022-01349-4,Oleylammonium capped cesium lead iodide quantum dots (~4.9 nm),C18H37N-CsPbI3,\"Cesium lead iodide, Cesium lead iodide with oleylamine\",C18H37N,CsPbI3,cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium,3,film,,,,,,,,\"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",CsPbI3 quantum dots,\"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \r\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190°C). \r\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",Pump-pulse spectroscopy,\"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\"\r\nDOI: 10.1002/anie.201702825,\"N,N′-dimethylethylene diaminium tin bromide\",C4H14N2SnBr4,\"N,N‚Ä≤-dimethylethylene diaminium tetrabromostannate(II), C4N2H14SnBr4\",C4H14N2,\"SnBr4, Tin bromide\",\"N,N′-dimethylethylene diaminium tin (II) bromide\",1,single crystal,,,,,,,,\"Tin(II) bromide (SnBr2), hydrobromic acid (HBr, 48 wt. % in H2O), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), N, N’-dimethylethylenediamine (99 %)\",colorless needle-like C4N2H14SnBr4 crystals,\"0.5 mmol Tin(II) bromide was dissolved in 3 ml HBr and 1 ml H3PO2. Under N2, the solution was heated up to 120 °C with constant magnetic stirring. 0.5 mmol N, N’-dimethylethylenediamine was injected into the hot solution and then the solution was cooled down to room temperature. The solids were collected.\",Single crystal X-ray diffraction,Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo Kα radiation (= 0.71073 Å) was used for single crystal diffraction at 100 K.\r\ndoi:10.1016/S0022-4596(03)00352-9,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,N/A,CH3ND3PbBr3 powder,\"Samples were prepared following well-described methods [1,2]. \r\n\r\nIn the case of the neutron sample, N-deuterated MAPB was produced by using fully deuterated DBr (MSD Isotopes), and reactor grade (499.8%) D2O (Atomic Energy of Canada Limited—AECL). The D2O was also used to deuterate all exchangeable hydrogens of the precursor chemicals prior to the final synthesis. A fine bright orange precipitate was formed which was filtered and transferred to a desiccating chamber prior to the diffraction measurements.\",Powder neutron diffraction,\"C2 diffractometer at Chalk River Laboratories, Chalk River, Ontario. The incident wavelength for Rietveld refinements: 1.32860(3)A˚. Data were collected and refined in two separate banks from 3–83° and 37–117° theta with wire-spacing 0.1° over the temperature range of 11–250K. Each bank was collected for 1 h. Refer to Page 104 Table 4.\"\r\ndoi:10.1016/S0022-4596(03)00352-9,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,N/A,CH3ND3PbBr3 powder,\"Samples were prepared following well-described methods [1,2]. \r\n\r\nIn the case of the neutron sample, N-deuterated MAPB was produced by using fully deuterated DBr (MSD Isotopes), and reactor grade (499.8%) D2O (Atomic Energy of Canada Limited—AECL). The D2O was also used to deuterate all exchangeable hydrogens of the precursor chemicals prior to the final synthesis. A fine bright orange precipitate was formed which was filtered and transferred to a desiccating chamber prior to the diffraction measurements.\",Powder neutron diffraction,\"C2 diffractometer at Chalk River Laboratories, Chalk River, Ontario. The incident wavelength for Rietveld refinements: 1.32860(3)A˚. Data were collected and refined in two separate banks from 3–83 ° and 37–117 ° 2theta with wire-spacing 0.1 ° over the temperature range of 11–250K. Each bank was collected for 1 h. Refer to Page 104 Table 4.\"\r\ndoi:10.1016/S0022-4596(03)00352-9,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,N/A,CH3ND3PbBr3 powder,\"Samples were prepared following well-described methods [1,2]. \r\n\r\nIn the case of the neutron sample, N-deuterated MAPB was produced by using fully deuterated DBr (MSD Isotopes), and reactor grade (499.8%) D2O (Atomic Energy of Canada Limited—AECL). The D2O was also used to deuterate all exchangeable hydrogens of the precursor chemicals prior to the final synthesis. A fine bright orange precipitate was formed which was filtered and transferred to a desiccating chamber prior to the diffraction measurements.\",Powder neutron diffraction,\"C2 diffractometer at Chalk River Laboratories, Chalk River, Ontario. Incident wavelength for Rietveld refinements: 1.32860(3)A˚. Data were collected and refined in two separate banks from 3–83 ° and 37–117 ° 2theta with wire-spacing 0.1 ° over the temperature range of 11–250K. Each bank was collected for 1 h. Refer to Page 104 Table 4.\"\r\ndoi:10.1016/S0022-4596(03)00352-9,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,powder,,,,,,,,,MAPbBr3 Powder,\"Samples were prepared following well-described\r\nmethods [1,2].\",Powder X-ray diffraction,\"X-ray diffraction measurements were performed from 120K to room temperature on samples mounted in 0.1mm diameter capillaries, mounted in an Enraf-Nonius Guinier-Simon camera, using CuKa_1 radiation. Refer to Page 98 Experimental.\"\r\ndoi:10.1021/jz5012109,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,\"HI (conc), PbAc2, CH3NH3+\",Black MAPbI3 Crystals,\"Precipitate product from a concentrated aqueous solution of hydroiodic acid containing lead(II) acetate and a respective amount of CH3NH3+ solution.\r\n\r\nThe two ends of the sample holder were held at 55 and 42 °C respectively to induce the saturation of the solute at the low temperature part of the solution. After 24 h submillimeter sized crystals appeared in the solution.\",Thermocouple: Temperature dependence of thermal conductivity,Conducted for 3 samples. Swept down from 310 K to 25 K. Using a steady-state method using calibrated stainless steel as reference sample (Page 2491 Figure 5). Refer to Page 2489 Figure 4.\r\ndoi:10.1021/jz5012109,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,bulk polycrystalline,,,,,,,,\"HI (conc), PbAc2, CH3NH3+\",Black MAPbI3 Crystals,\"Precipitate product from a concentrated aqueous solution of hydroiodic acid containing lead(II) acetate and a respective amount of CH3NH3+ solution.\r\n\r\nThe two ends of the sample holder were held at 55 and 42 °C respectively to induce the saturation of the solute at the low temperature part of the solution. After 24 h submillimeter sized crystals appeared in the solution.\",Thermocouple: Temperature dependence of thermal conductivity,Conducted for 3 samples. Swept down from 310 K to 25 K. Using a steady-state method using calibrated stainless steel as reference sample (Page 2491 Figure 5). Refer to Page 2489 Figure 4.\r\ndoi:10.1002/adma.201501978,Methylammonium bismuth iodide,CH3NH3Bi2I9,Tris(methanaminium) nonaiodo dibismuthate(III),CH3NH3,\"Bi2I9, Bismuth iodide\",methylaminium bismuth iodide,0,film,,,,,,,,\"CH3NH3I, BiI3\",MA3Bi2I9 film,\"A mixture of CH3NH3I (2.475 M) and BiI3 (1.65 M) in dimethylformamide (DMF)/dimethyl sulfoxide (DMSO) solvent mixture (7/3 by volume) was used to synthesize MA3Bi2I9. The solution was spin-coated onto TiO 2 / glass substrate at 1500 rpm for 20 s, followed by annealing on a hot plate at 110 °C for 30 min.\",Photoluminescence,The spectrum was recorded using Fluorolog-3 instrument (Horiba Jobin Yvon).\r\nhttps://doi.org/10.1002/adma.201501978,Cesium bismuth iodide,CH3NH3Bi2I9,Tricesium nonaiodo dibismuthate(II),CH3NH3,\"Bi2I9, Bismuth iodide\",,0,film,,,,,,,,\"CsI, BiI3\",Cs3Bi2I9 film,\"A mixture of Cs(2.475 M) and BiI3 (1.65 M) in dimethylformamide (DMF)/dimethyl sulfoxide (DMSO) solvent mixture (7/3 by volume) was used to synthesize Cs3Bi2I9. The solution was spin-coated onto TiO 2 / glass substrate at 1500 rpm for 20 s, followed by annealing on a hot plate at 110 °C for 30 min.\",Photoluminescence,The spectrum was recorded using Fluorolog-3 instrument (Horiba Jobin Yvon).\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3,\"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",C8H12N,\"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",Photoluminescence spectroscopy,Photoluminescence spectra were measured on crystal films using a Horiba iHR320 spectroscopy device and a 337 nm SRS NL100 nitrogen laser.\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3,\"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",C8H12N,\"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",Electroluminescence spectroscopy,Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2were prepared for this experiment.\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3,\"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",C8H12N,\"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",Electroluminescence spectroscopy,Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2 were prepared for this experiment. The external quantum efficiency can then be calculated using the EL spectrum with the Lambertian profile.\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3,\"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",C8H12N,\"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",Electroluminescence spectroscopy,Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2were prepared for this experiment. The external quantum efficiency can then be calculated using the EL spectrum with the Lambertian profile.\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.2, y = 0.4\",C16H24N2Rb0.2Cs0.8PbBr2.6Cl0.4,\"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4, (C8H12N)2RbCsPbBrCl\",C8H12N,Rb0.2Cs0.8PbBr2.6Cl0.4,bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.2Cs0.8PbBr2.6Cl0.4 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M). Different fractional compounds were created by mixing these solutions in certain ratios.\",Photoluminescence spectroscopy,\"Photoluminescence quantum efficiency (PLQE) was measured through the use of a Labsphere QE sphere, or an integrating sphere, connected to an Ocean Optics QEpro, which is a photoluminescence spectrometer. The excitation source was a 405 nm continuous laser at an intensity of 0.17 mW/(cm^2). Experiments were performed at room temperature with perovskite films on glass.\"\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3,\"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",C8H12N,\"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",Photoluminescence spectroscopy,Photoluminescence spectra were measured on crystal films using a Horiba iHR320 spectroscopy device and a 337 nm SRS NL100 nitrogen laser.\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.2, y = 0.4\",C16H24N2Rb0.2Cs0.8PbBr2.6Cl0.4,\"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4, (C8H12N)2RbCsPbBrCl\",C8H12N,Rb0.2Cs0.8PbBr2.6Cl0.4,bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.2Cs0.8PbBr2.6Cl0.4 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M). Different fractional compounds were created by mixing these solutions in certain ratios.\",Electroluminescence spectroscopy,Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2 were prepared for this experiment.\r\nhttps://doi.org/10.1002/adma.202100783,\"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.2, y = 0.4\",C16H24N2Rb0.2Cs0.8PbBr2.6Cl0.4,\"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4, (C8H12N)2RbCsPbBrCl\",C8H12N,Rb0.2Cs0.8PbBr2.6Cl0.4,bis(phenethylaminium) rubidium cesium lead(II) bromide chloride,2,film,,,,,,,,\"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",PEA2Rb0.2Cs0.8PbBr2.6Cl0.4 film,\"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M). Different fractional compounds were created by mixing these solutions in certain ratios.\",Electroluminescence spectroscopy,Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2 were prepared for this experiment. The external quantum efficiency can then be calculated using the EL spectrum with the Lambertian profile.\r\nhttps://doi.org/10.1002/anie.201910800,Cesium lead iodide,CsPbI3,\"cesium lead iodide, cesium triiodoplumbate(II)\",None,CsPbI3,cesium lead(II) iodide,3,film,,,,,,,,\"CsI, PbI2, DMAI\",thin film of CsIPbI3:xDMAI,\"CsI, PbI2, xDMAI (Dimethylammonium Iodide) were dissolved at a 1:1:x molar ratio (with x = 0.5, 0.7, 1.0 and 1.5) in DMF to prepare the CsPbI3:xDMAI-precursor. The active layer was spin-coated onto a 70°C warm c-TiO2/FTO substrate at 3000 rpm for 30s. Annealing was done at 150°C for 2 minutes for x = 0.5 and for 10 minutes for x = 0.7, as well as at 210°C for 5 minutes for x = 1.0 and 1.5. Experiments were done in a dry box with 5-10% RH.\",UV-Vis spectroscopy,None stated\r\nhttps://doi.org/10.1002/anie.201915422,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,2,film,,,,,,,,\"PbI2, MAI\",thin film,\"The film is produced using a dynamic two-step deposition method. on a compact TiO2/ATO substrate, a N,N-dimethylformamide (DMF) solution of PbI2 is spin coated at 3000 rpm for 10 s, and an isopropyl alcohol solution of methylammonium iodide (MAI) is immediately added dropwise, while keeping the whole spinning time 20 s prior to the end of spin coating. The yellow PbI2 solution turns to brown immediately and gradually darkens during the spin coating. After annealing at 150 °C for 10 min, the as-prepared perovskite film has a shiny black color due to the high visible light absorption and super flat surface. The cross-linking agent 2-aminoterephthalic acid (with different concentrations of 0, 0.2, 0.5, and 1 mg mL−1) was immediately spin-coated on the MAPbI3 film and subsequently annealed at 150 °C for 5 min.\",UV-Vis absorption,\"The absorption spectra were collected by a UV-visible spectrophotometer (UV-3600, Shimadzu Corp.)\"\r\nhttps://doi.org/10.1002/anie.201915422,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,2,film,,,,,,,,\"PbI2, MAI\",thin film,\"The film is produced using a dynamic two-step deposition method. on a compact TiO2/ATO substrate, a N,N-dimethylformamide (DMF) solution of PbI2 is spin coated at 3000 rpm for 10 s, and an isopropyl alcohol solution of methylammonium iodide (MAI) is immediately added dropwise, while keeping the whole spinning time 20 s prior to the end of spin coating. The yellow PbI2 solution turns to brown immediately and gradually darkens during the spin coating. After annealing at 150 °C for 10 min, the as-prepared perovskite film has a shiny black color due to the high visible light absorption and super flat surface. The cross-linking agent 2-aminoterephthalic acid (with different concentrations of 0, 0.2, 0.5, and 1 mg mL−1) was immediately spin-coated on the MAPbI3 film and subsequently annealed at 150 °C for 5 min.\",UV-Vis absorption,\"The absorption spectra were collected by a UV-visible spectrophotometer (UV-3600, Shimadzu Corp.)\"\r\nhttps://doi.org/10.1002/anie.202003509,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%)\",(PEA)2SnI4 crystals,\"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 ˚C under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration and were stored in an N2 glove box.\",UV-visible absorption,\"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using the Kubelka-Munk transformation; (α/S = (1 − R)^2/2R); α is the absorption coefficient, S is the scattering coefficient, and R is the reflectance.\"\r\nhttps://doi.org/10.1002/anie.202003509,Bis(dodecylammonium) lead iodide,C24H56N2PbI4,\"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",C12H28N,\"PbI4, Lead iodide\",bis(dodecyl-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"Lead(II) oxide (Sigma Aldrich, 99.9%), decylamine (Sigma Aldrich, 99%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%)\",(DA)2PbI4 crystals,\"(DA)2PbI4 single crystals were synthesized by dissolving lead oxide (0.5 mmol) in  20 mL of hydriodic acid by heating to boiling under constant stirring. To it, 0.5 mmol of decylamine was added. The solution was heated and stirred until the precipitate dissolved completely. Then the solution was allowed to cool naturally to room temperature.\",UV-visible absorption,UV-Visible absorbance data were recorded on the transmission mode in Cary Series UV-Vis Spectrophotometer (Agilent Technologies).\r\nhttps://doi.org/10.1002/anie.202003509,Bis(Butylammonium) lead iodide : Iodine-intercalated,C8H24N2PbI4:I2,\"(C4H9NH3)2PbI4:I2, (C4H12N)2PbI4:I2, BA2PbI4:I2, (BA)2PbI4:I2, I2-intercalated bis(butane-1-aminium) tetraiodoplumbate(II)\",C4H12N,\"PbI4, Lead iodide\",I2-intercalated bis(butane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I, I2\",(BA)2PbI4:I2,\"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether. Dried (BA)2PbI4 crystals were placed in an open plastic tube which was kept in a closed glass vial containing molecular I2 for 2-3 hours at room temperature.\",UV-vis absorption,\"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using Kubelka-Munk transformation: (α/S = (1 − R)^2/2R); α is the absorption coefficient, and S is the scattering coefficient R is the reflectance.\"\r\nhttps://doi.org/10.1002/anie.202003509,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I\",(BA)2PbI4,\"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether.\",UV-visible absorption,\"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using the Kubelka-Munk transformation; (α/S = (1 − R)^2/2R); α is the absorption coefficient, S is the scattering coefficient, and R is the reflectance.\"\r\nhttps://doi.org/10.1002/anie.202003509,Bis(Butylammonium) lead iodide : Iodine-intercalated,C8H24N2PbI4:I2,\"(C4H9NH3)2PbI4:I2, (C4H12N)2PbI4:I2, BA2PbI4:I2, (BA)2PbI4:I2, I2-intercalated bis(butane-1-aminium) tetraiodoplumbate(II)\",C4H12N,\"PbI4, Lead iodide\",I2-intercalated bis(butane-1-aminium) lead (II) iodide,2,single crystal,,,,,,,,\"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I, I2\",(BA)2PbI4:I2,\"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether. Dried (BA)2PbI4 crystals were placed in an open plastic tube which was kept in a closed glass vial containing molecular I2 for 2-3 hours at room temperature.\",Photoluminescence,Recorded on FLS 980 (Edinburgh Instruments).\r\nhttps://doi.org/10.1002/anie.202003509,Bis(Butylammonium) lead iodide,C8H24N2PbI4,\"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",C4H12N,\"PbI4, Lead iodide\",bis(butane-1-aminium) lead(II) iodide,2,single crystal,,,,,,,,\"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I\",(BA)2PbI4,\"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether.\",Photoluminescence,Recorded on FLS 980 (Edinburgh Instruments).\r\nhttps://doi.org/10.1002/anie.202003509,Hexaflourobenzene bis(phenethylammonium) tin iodide,C16H24N2SnI4:C6F6,\"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\"C8H12N, C6F6\",\"SnI4, Tin iodide\",hexafluorobenzene bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%), hexafluorobenzene (HFB, Sigma Aldrich, 99%)\",(PEA)2SnI4 : HFB crystals,\"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 ˚C under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration. 50 mg of these crystals was dissolved in a mixture of 2 mL methanol and 2 mL HFB. The obtained dark yellow solution was kept open in a glove box. As the solvent evaporates (PEA)2SnI4:HFB crystals precipitate out. The crystals were filtered, dried and stored in a glove box for further use.\",UV-visible absorption,\"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using the Kubelka-Munk transformation; (α/S = (1 − R)^2/2R); α is the absorption coefficient, S is the scattering coefficient, and R is the reflectance.\"\r\nhttps://doi.org/10.1002/anie.202003509,Hexaflourobenzene bis(phenethylammonium) tin iodide,C16H24N2SnI4:C6F6,\"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\"C8H12N, C6F6\",\"SnI4, Tin iodide\",hexafluorobenzene bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%), hexafluorobenzene (HFB, Sigma Aldrich, 99%)\",(PEA)2SnI4 : HFB crystals,\"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 ˚C under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration. 50 mg of these crystals was dissolved in a mixture of 2 mL methanol and 2 mL HFB. The obtained dark yellow solution was kept open in a glove box. As the solvent evaporates (PEA)2SnI4:HFB crystals precipitate out. The crystals were filtered, dried and stored in a glove box for further use.\",Photoluminescence,Recorded on FLS 980 (Edinburgh Instruments).\r\nhttps://doi.org/10.1002/anie.202003509,Bis(phenethylammonium) tin iodide,C16H24N2SnI4,\"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",C8H12N,\"SnI4, Tin iodide\",bis(phenylethanaminium) tin iodide,2,single crystal,,,,,,,,\"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%)\",(PEA)2SnI4 crystals,\"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 ˚C under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration and were stored in an N2 glove box.\",Photoluminescence,Recorded on FLS 980 (Edinburgh Instruments).\r\nhttps://doi.org/10.1002/solr.201900374,Propylammonium iodide,CH3(CH2)2NH3I,C3AI,C3NH10,\"I, iodide\",propylaminium iodide,3,single crystal,,,,,,,,n-propylamine with hydriodic acid (HI) (57wt% in water),CH3(CH2)2NH3I (C3AI),C3AI was synthesized by evaporating a mixture of n-propylamine with hydriodic acid at 0 °C and recrystallizing the product in ethanol.3,,\r\nhttps://doi.org/10.1002/solr.201900374,Propylammonium iodide,CH3(CH2)2NH3I,C3AI,C3NH10,\"I, iodide\",propylaminium iodide,3,single crystal,,,,,,,,,,,,\r\nhttps://doi.org/10.1006/jssc.1999.8281,Bis(phenylethylammonium) lead chloride,C16H24N2PbCl4,\"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",C8H12N,\"PbCl4, Lead chloride\",bis(2-phenylethan-1-aminium) lead (II) chloride,2,single crystal,,,,,,,,\"PbCl2, HCl, methanol, phenethylamine\",Small block-like crystals to larger plate-like crystals,\"Layered solution approach.\r\n\r\nGrow crystals within a long, straight, glass tube (Refer to Fig. 1). First dissolve 1.0 mmol (0.278 g) of freshly sublimed PbCl2 (Aldrich; 99.999%) in 7.5 ml concentrated (37 wt %) aqueous HCl (Aldrich; 99.999%). Weigh and add PbCl2 to the tube in an argon-filled glove box, with oxygen and water levels maintained below 1 ppm. Cover the tube with a septum before removing the glove box and adding HCl with a syringe. \r\n\r\nCreate a second layer in the crystal tube by gently syringing 15 ml of methanol (Aldrich; anhydrous, 99.8%) on top of the HCl/PbCl2 solution. A relatively sharp interface can be created between the solvent layers due to density differences. On top of the column, add a stoichiometric amount (2 mmol or approximately 0.25 ml) of phenethylamine with a syringe. \r\n\r\nIn the experiment, the phenethylamine rapidly dispersed in the methanol but, because of the sharp interface with the HCl solution, formation of the final (C6H5C2H4NH3)2PbCl4 product was very slow. The crystals were isolated after approximately one year by removing the solvent with a syringe and drying the crystals under vacuum at room temperature and later stored in an argon glove box.\",Single-crystal X-ray diffraction,\"A colorless single crystal of dimensions 0.09 mm X 0.18 mm X 0.27 mm was used. A full sphere of data was collected at room temperature on a Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo Kα radiation, λ = 0.71073 Å). Refer to page 695 for details.\"\r\nhttps://doi.org/10.1016/j.jallcom.2020.156790,Calcium tin sulfide,CaSnS3,\"Calcium trisulfostannate(II), CaSnS3\",None,SnS3,,3,film,,,,,,,,,,,,\r\nhttps://doi.org/10.1016/j.mseb.2004.12.052,Bis(butylammonium) copper chloride,C8H24N2CuCl4,\"(C4H9NH3)2CuCl4, bis(butan-1-aminium) tetrachlorocuprate(II)\",C4H12N,\"CuCl4, Copper chloride\",bis(butan-1-aminium) copper chloride,2,film,,,,,,,,,,\"The organic–inorganic hybrid perovskite, (C4H9NH3)2CuCl4, was prepared by the reaction of butylammonium chloride, C4H9NH3Cl, with a stoichiometric amount of copper chloride. Firstly, anhydrous CuCl2 powder was added to the solution of C4H9NH3Cl in anhydrous ethanol, and the reaction mixture was stirred and refluxed for 1 h. The solvent was then evaporated completely, giving golden solids. The solids were recrystallized in anhydrous ethanol and dried at 80 °C in vacuum, obtaining (C4H9NH3)2CuCl4 as golden sheet-like crystals. Calcd for C8H24N2CuCl4: C, 27.16%; N, 7.92%; H, 6.79%. Found: C, 27.21%; N, 7.84%; H, 6.66%.\r\n\r\nThe (C4H9NH3)2CuCl4 film was prepared by spin-coating a solution (10 mg/ml) of (C4H9NH3)2CuCl4 in anhydrous ethanol on a quartz substrate at a speed of 800 rpm for 30 s, followed by annealing at 80 °C in vacuum for 1 h. The film thickness was tested about 100 nm.\",,\r\nhttps://doi.org/10.1016/j.nanoen.2017.05.005,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,film,,,,,,,,\"CsBr, PbBr2, DMSO\",CsPbBr3,The hybrid perovskite CsPbBr3 was prepared from a mixture of CsBr and PbBr2 that was dissolved in a DMSO solvent. The thin films of CsPbBr3 were produced at room temperature via spin-coating and with the addition of chlorobenzene to the mixture.,Luminance of devices,CsPbBr3 thin-film LED samples were displayed to observe the luminance by measuring the wavelength density power emitted by the light source.\r\nhttps://doi.org/10.1021/acs.chemmater.6b03944,Bis(methylammonium) silver bismuth bromide,(CH3NH3)2AgBiBr6,\"Bis(methanaminium) tribromoargentate(I) tribromobismuthate(III), (MA)2AgBiBr6\",CNH6,AgBiBr6,*,3,single crystal,,,,,,,,\"CH3NH3Br (synthesized from CH3NH3 and HBr), AgBr (synthesized from AgNO3 and KBr in H2O), BiBr3, PbBr2\",Red crystals,\"0.112 g of CH3NH3Br, 0.094 g of AgBr, and 0.2243 g of BiBr3 (2:1:1 molar ratio) were loaded in an autoclave with 0.5 mL of a HBr (48% in H2O) acid solution. Additionally, 0.011 g of CH3NH3Br and 0.036 g of PbBr2 (1:1 molar ratio) were taken. The solution was heated at 433 K for 3 days and then slowly cooled to room temperature in 3 h.\",UV vis absorption (diffuse reflectance),PerkinElmer Lambda 750 UV-Visible spectrometer was used to measure the optical absorption measurements on a scan range was between 350 and 1300nm.\r\nhttps://doi.org/10.1021/acs.chemmater.6b03944,Bis(methylammonium) silver bismuth bromide,(CH3NH3)2AgBiBr6,\"Bis(methanaminium) tribromoargentate(I) tribromobismuthate(III), (MA)2AgBiBr6\",CNH6,AgBiBr6,*,3,single crystal,,,,,,,,\"CH3NH3Br (synthesized from CH3NH3 and HBr), AgBr (synthesized from AgNO3 and KBr in H2O), BiBr3, PbBr2\",Red crystals,\"0.112 g of CH3NH3Br, 0.094 g of AgBr, and 0.2243 g of BiBr3 (2:1:1 molar ratio) were loaded in an autoclave with 0.5 mL of a HBr (48% in H2O) acid solution. Additionally, 0.011 g of CH3NH3Br and 0.036 g of PbBr2 (1:1 molar ratio) were taken. The solution was heated at 433 K for 3 days and then slowly cooled to room temperature in 3 h.\",Single crystal X-ray diffraction,\"Frames were collected using an Oxford Gemini E Ultra diffractometer, Mo Kα radiation (λ = 0.71073Å), equipped with an Eos CCD detector.\"\r\nhttps://doi.org/10.1021/acs.chemmater.8b01200,4-methylpiperidinium bismuth iodide: triiodide,(C6H14N)4I3BiI6,\"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",C6H14N,\"I3BiI6, Iodide bismuth iodide\",tetrakis(4-methylpiperidinium) iodide bismuth iodide,0,single crystal,,,,,,,,\"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",black needle-like crystals,\"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days. The crystals were redissolved in an oxidized HI solution, and the solution was again allowed to be evaporated over a few days.\",Single crystal X-ray diffraction,SCXRD data were collected using an Agilent SuperNova Dual diffractometer equipped with a graphite-monochromatized Mo Kα radiation (λ = 0.71073 Å)\r\nhttps://doi.org/10.1021/acs.chemmater.8b01200,4-methylpiperidinium bismuth iodide: triiodide,(C6H14N)4I3BiI6,\"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",C6H14N,\"I3BiI6, Iodide bismuth iodide\",tetrakis(4-methylpiperidinium) iodide bismuth iodide,0,powder,,,,,,,,\"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",black needle-like crystals,\"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days. The crystals were redissolved in an oxidized HI solution, and the solution was again allowed to be evaporated over a few days.\",Thermogravimetric analysis,The experiment was performed using a Netzsch TG 209 F1 Libra Thermo- Microbalance with alumina pans at a heating rate of 10 °C/min.\r\nhttps://doi.org/10.1021/acs.chemmater.8b01200,4-methylpiperidinium bismuth iodide: triiodide,(C6H14N)4I3BiI6,\"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",C6H14N,\"I3BiI6, Iodide bismuth iodide\",tetrakis(4-methylpiperidinium) iodide bismuth iodide,3,single crystal,,,,,,,,,,,Differential scanning calorimetry measurements (DSC),A Netzsch TG 209 FI Libra Thermomirobalance system was used at a heating rate of 100 °C/min was used to analyze the crystal samples (10 mg) thermogravimetric and differential thermal aspects.\r\nhttps://doi.org/10.1021/acs.chemmater.8b01200,4-methylpiperidinium bismuth iodide: triiodide,(C6H14N)4I3BiI6,\"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",C6H14N,\"I3BiI6, Iodide bismuth iodide\",tetrakis(4-methylpiperidinium) iodide bismuth iodide,0,single crystal,,,,,,,,\"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",black needle-like crystals,\"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days. The crystals were redissolved in an oxidized HI solution, and the solution was again allowed to be evaporated over a few days.\",UV-vis absorbance (diffuse reflectance),The reflectance spectrum was collected using a LAMBDA 950 UV/vis spectrophotometer. Reflectance was converted to absorbance using the Kubelka–Munk function.\r\nhttps://doi.org/10.1021/acs.chemmater.8b01200,4-methylpiperidinium bismuth iodide,(C6H14N)3Bi2I9,\"MP-Bi2I9, tris(4-methylpiperidinium) nonaiodo dibismuthate(III)\",C6H14N,\"Bi2I9, Bismuth iodide\",tris(4-methylpiperidinium) bismuth iodide,0,single crystal,,,,,,,,\"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",red needle-like crystals,\"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days.\",UV-vis absorbance (diffuse reflectance),The reflectance spectrum was collected using a LAMBDA 950 UV/vis spectrophotometer. Reflectance was converted to absorbance using the Kubelka–Munk function.\r\nhttps://doi.org/10.1021/acs.joc.9b02769,\"thieno[3,2-b]thiophene\",C6H4S2,TbT,C6H4,S2,,3,single crystal,,,,,,,,\"Ether (700 mL), 3-(2,2-diethoxy-ethylsulfanyl)thiophene, 1.5 M tert-butyllithium e (400 mL, 0.600 mol)\",\"Thieno[3,2-b]thiophene\",\"3-(2,2-diethoxy-ethylsulfanyl)thiophene (32.8 g, 154 mmol) was stirred with a solution of ether (700 mL) and was heated for 10 h. The mixture was then filtered via a Buchner Funnel filter. The solvent was then removed and the residue was purified by column chromatography on silica gel. This process produced Thieno[3,2-b]thiophene.\",Absorbance spectra,UV-Visible spectrophotometer in CH2Cl2 solution was collected on a Nicolet AVATAR 360 FT-IR instrument.\r\nhttps://doi.org/10.1021/acs.jpclett.6b00793,\"N-methylethane-1,2-diammonium lead bromide\",C3H12N2PbBr4,\"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",C3H12N2,\"PbBr4, Lead bromide\",\"N-methylethane-1,2-diaminium lead(II) bromide\",3,powder,,,,,,,,\"N,N-dimethylformamide\",(N-MEDA)[PbBr4],\"Films of (N-MEDA)[PbBr4] were produced by dissolved 0.1 M of (N-MEDA)[PbBr4] in an N, N-dimethylformamide via starting at 3000 rpm. Single crystals were yielded from annealing the solution at 100 °C for 10 minutes. Depressing ball-milled powder at a pressure of 10,000-15,000 psi produced the pellet samples.\",Time-Correlated Single Photon Counting (TCSPC) measurement,A fiber laser tripled from a wavelength range of 1030 nm to 343 nm was used to excite a single crystal pellet sample of  (N-MEDA)[PbBr4]. The TCSPC system was set at a pulse duration of 500-f and a repetition rate of 1.28-MHz. A  hybrid photomultiplier detector assembly was used to observe the PL intensity via  fluorescence bandpass filters and  reflective neutral density\r\nhttps://doi.org/10.1021/acs.jpclett.7b00086,Aniline copper bromide iodide,C6H6NCuBr2I,\"C6H4NH2CuBr2I, aniline monobromo diiodocuprate(II)\",C6H6N,\"CuBr2I, Copper bromide iodide\",aniline copper bromide iodide,2,film,,,,,,,,\"CuBr2 (Copper bromide,99.999% Sigma-Aldrich), C6H4NH2I (2-iodoaniline, 98% Aladdin), N, N-Dimethylformamide, FTO substrate\",500 nm thick C6H4NH2CuBr2I thin-film on FTO glass,\"An equimolar mixture of C6H4NH2I (547.55 mg) and CuBr2 (558.75 mg) was dissolved in N, N-Dimethylformamide (1 mL) by stirring at 60 °C overnight. The solution was ultrasonicated for 30 min and filtered by PTFE syringe filters (0.45 μm).\r\nThe obtained solution was spin-coated at 1500 rpm for 30 s, followed by annealing on a hot plate at 70 °C for 30 min.\",UV-vis absorption,The spectrum was measured using PerkinElmer Lambda 950 spectrophotometer. Tauc plot with direct band gap assumption was used to obtain the band gap.\r\nhttps://doi.org/10.1021/acs.nanolett.5b02082,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,3,nanoform,,,,,,,,\"CH3NH3Br (5- 9 mg/mL), Anhydrous isopropanol (4 mL), PEDOT:PSS, Aldrich ( 10 µL)\",CH3NH3PbBr3 Nanorod Arrays,\"ITO substrated was coated with PEDOT: PSS (Clevios) at 3000 rpm for 40 seconds and followed by heating at 150 °C for 15 minutes. Using a methanolic solution, ITO substrated was coated with 10 µL of lead acetate trihydrate (Aldrich). The chips formed were heated at  65°C and stored in a glove box filled with nitrogen gas. Then CH3NH3Br ( 5 mg/mL to 9 mg/mL ) was dissolved in n 4 mL of anhydrous\r\nisopropanol (Aldrich), which was mixed with ITO/PEDOT: PSS/lead acetate substrate. An orange film began to grow on the substrate and CH3NH3PbBr3 arrays were produced.\",UV-Vis spectrometer,\"Chips of CH3NH3PbBr3 were placed into a vial, in which they were hooked to a cable tie and submerged into an oil bath at 140 to 150 °C. The vial contained 0.1g of CH3NH3I which enabled direct contacts between the solutions. Partial anion exchange was achieved because of the separation of CH3NH3X and PbX2. The electroluminescence was observed were observed from the from hybrid perovskite nanocrystals blended with a thin polyimide dielectric polymer using a Shimadzu UV-3101 UV-Vis spectrometer equipped with an integrating sphere.\"\r\nhttps://doi.org/10.1021/acs.nanolett.5b02082,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,single crystal,,,,,,,,CH3NH3PbBr3,CH3NH3PbI3,The hybrid perovskite (CH3NH3PbBr3) was converted at low temperature via anion exchange to produce a CH3NH3PbI3.,I-V Test Device,\"The I-V characteristics of CH3NH3PbI3 were determined by using a Keithley 2636 source-measure unit, which was coupled to a 60X objective in an inverted microscope. This was performed by with a set up of a 100 ms pulse as the device was electrically contacted a soft probe (Picoprobe T 4-10)\r\ncoated with indium gallium eutectic (Aldrich).\"\r\nhttps://doi.org/10.1021/acs.nanolett.6b04453,Methylammonium lead bromide iodide,CH3NH3PbBr(x)I(3-x),\"MAPb(Br,I)3, MAPbBr(x)I(3-x), MAPbBrI, MAPI alloy\",CH3NH3,\"PbBr(x)I(3-x), Lead bromide iodide\",Methanaminium lead bromide iodide,3,single crystal,,,,,,,,\"PbBr2 (Aldrich), CH3NH3Br (Dyesol) , PbI2 (Aldrich), CH3NH3I (Dyesol), DMF (Aldrich)\",CsPb(BrxI1-x)3,CsPbBr3 was synthesized from a solution containing 0.3 M of CsBr (Aldrich)/PbBr2 and CsI (Aldrich)/PbI2 in DMSO. Films of CsPbBr3 were obtained from heating and annealing the solution at 150 °C and 75 °C.,Confocal microscopy and photoluminescence (PL) spectra,The temperature dependence of phase separation with PL was measured by observing the time it took for the PL peak of  iodide-rich clusters of the compound films to reach the maximum value.\r\nhttps://doi.org/10.1021/acs.nanolett.6b04453,Methylammonium lead bromide iodide,CH3NH3PbBr(x)I(3-x),\"MAPb(Br,I)3, MAPbBr(x)I(3-x), MAPbBrI, MAPI alloy\",CH3NH3,\"PbBr(x)I(3-x), Lead bromide iodide\",Methanaminium lead bromide iodide,3,single crystal,,,,,,,,\"PbBr2 (Aldrich), CH3NH3Br (Dyesol) , PbI2 (Aldrich), CH3NH3I (Dyesol), DMF (Aldrich)\",CsPb(BrxI1-x)3,CsPbBr3 was synthesized from a solution containing 0.3 M of CsBr (Aldrich)/PbBr2 and CsI (Aldrich)/PbI2 in DMSO. Films of CsPbBr3 were obtained from heating and annealing the solution at 150 °C and 75 °C.,Photoluminescence Spectra,The Photoluminescence Spectra method was used to measure the normalized PL intensity versus time of the iodide cluster peak by using an excitation source of 405 nm LED.\r\nhttps://doi.org/10.1021/acs.nanolett.7b01544,Formamidinium lead bromide,CH5N2PbBr3,\"Methanimidamide tribromoplumbate(II), FAPBr3, FAPBr, (FA)PbBr3 HC(NH2)2PbBr3, (NH2)2CHPbBr3\",CH5N2,\"PbBr3, Lead bromide\",Imidoformamidinium lead(II) bromide,2,single crystal,,,,,,,,\"FABr (0.53M),  PbBr2 (0.4 M), Ethanol, OLA (625 μL), OA (25 μL),  (Toluene, 12.5 mL\",FAPbBr3,\"The 2D perovskite FAPbBr3 was synthesized from a solution that included FABr ( 625 μL)dissolved in a non-polar toluene solvent and a polar Ethanol solvent. The nonpolar solvent contained OA and OLA as organic surfactants, which stabilized the solutions. As a result, a precipitate of the solution formed from the poor solubility of perovskites in the nonpolar solvent. This yielded the final product of  FAPbBr3 nanoplatelets in 2.5 mL of Toluene, which was then dissolved in ethanol (375 μL) to produce higher and more stable concentrations of FAPbBr3 nanoplatelet.\",Photoluminescence Spectra,A CCD spectrometer was used to obtain the absolute absorbance of the colloidal solution in the non-polar solvent of Toluene. The PL of the colloidal solutions were obtained using the Quantaurus QY (C11347-11) from Hamamatsu.\r\nhttps://doi.org/10.1021/acs.nanolett.7b01544,Methylammonium lead bromide,CH3NH3PbBr3,\"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",CNH6,\"PbBr3, Lead bromide\",methanaminium lead(II) bromide,2,nanoform,,,,,,,,\"MABr (0.53 M) , PbBr2 (0.4 M), OLA (625 μL) and OA (25 μL), (Toluene, 12.5 mL)\",MAPbBr3,\"The 2D perovskite MAPbBr3 was synthesized from a solution containing MABr (0.53 M) and PbBr2 (0.4M), which was dissolved in a polar DMF solvent. This solution was then mixed with a non-polar Toluene solvent. As a result, a precipitate of MAPbBr3 was formed as nanoplatelets via crystallization.\",Photoluminescence Spectra,A CCD spectrometer was used to obtain the absolute absorbance of the colloidal solution in the non-polar solvent of Toluene. The PL of the colloidal solutions were obtained using the Quantaurus QY (C11347-11) from Hamamatsu.\r\nhttps://doi.org/10.1021/acsami.0c02313,Bis(butylammonium) lead chloride,C4H12N2PbCl4,\"Bis(butylaminium) tetrachloroplumbate(II), (BA)2PbCl4\",C4H12N,\"PbCl4, Lead chloride\",*,2,single crystal,,,,,,,,\"PbO powder, 57% w/w aqueous HI solution, butylamine, 50% aqueous H3PO2\",orange plate-like crystals,\"10 mmol PbO was dissolved in 16 mL HI at boiling temperature by stirring for ~5 min. Separately, 10 mmol butylamine was added to 1.7 mL H3PO2. The two solutions were mixed and the mixture was allowed to cool to room temperature.\",Single-crystal X-ray diffraction,Frames were collected using a STOE IPDS II/IPDS 2T diffractometer with Mo Kα radiation (λ = 0.710 73 Å) and operating at 50 kV and 40 Ma or Bruker Molly or Duo instrument with MoKα IμS microfocus source (λ= 0.71073 Å) with MX Optics.\r\nhttps://doi.org/10.1021/acscentsci.6b00055,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,single crystal,,,,,,,,,,,Single-Crystal X-ray Diffraction,\"Frames were collected using a Bruker D85 diffractometer equipped with a Photon 100 CMOS detector. Synchrotron X-rays at Beamline 11.3.1 at the ALS, LBNL were monochromated using silicon(111).\"\r\nhttps://doi.org/10.1021/acsenergylett.6b00327,Methylammonium lead iodide,CH3NH3PbI3,\"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",CH6N,\"PbI3, Lead iodide\",methanaminium lead(II) iodide,3,film,,,,,,,,,,,,\r\nhttps://doi.org/10.1021/acsnano.1c01134,Bis(R-)methylbenzylammonium copper chloride,C16N2H242CuCl4,R-MBA2CuCl4,C8NH12,CuCl4,bis(R-)methylbenzylaminium copper (II) chloride,2,single crystal,,,,,,,,\"(R)-(+)-α-methylbenzylamine (R-MBA), ethanol, HCl, diethyl ether, copper(II) chloride dihydrate\",Single crystals of Bis(R-)methylbenzylammonium copper chloride,\"The synthesis of a precursor solution, MBACl, was done by adding R-MBA (5 mL) and ethanol (15 mL) to a round-bottom flask (250 mL), and stirring the mixture at 0 degrees Celsius. HCl (10 mL, 37%) was added, and the solution was stirred for two hours. Then, copper(II) chloride dihydrate (171 mg, 1 mmol), MBACl (315 mg, 2 mmol), and isopropyl alcohol were added to a vial under heat and stirred until all solids dissolved. The resulting dark green solution cooled to room temperature, while green single crystals of Bis(R-)methylbenzylammonium copper chloride were precipitated. Crystals were washed by diethyl ether and vacuum-dried.\",Single-crystal X-ray diffraction,\"Single-crystal structure data was collected using a Bruker KAPPA APEX II diffractometer, APEX II CCD detector, and a Mo Kα source (λ = 0.71073 Å). APEX and Olex2 software was used for further refinement.\"\r\nhttps://doi.org/10.1021/acsnano.1c01134,Bis(S-)methylbenzylammonium copper chloride,C16N2H242CuCl4,S-MBA2CuCl4,C8NH12,CuCl4,bis(S-)methylbenzylaminium copper (II) chloride,2,single crystal,,,,,,,,\"(S)-(−)-α-methylbenzylamine (S-MBA), ethanol, HCl, diethyl ether, copper(II) chloride dihydrate\",Single crystals of Bis(S-)methylbenzylammonium copper chloride,\"The synthesis of a precursor solution, MBACl, was done by adding S-MBA (5 mL) and ethanol (15 mL) to a round-bottom flask (250 mL), and stirring the mixture at 0 degrees Celsius. HCl (10 mL, 37%) was added, and the solution was stirred for two hours. Then, copper(II) chloride dihydrate (171 mg, 1 mmol), MBACl (315 mg, 2 mmol), and isopropyl alcohol were added to a vial under heat and stirred until all solids dissolved. The resulting dark green solution cooled to room temperature, while green single crystals of Bis(S-)methylbenzylammonium copper chloride were precipitated. Crystals were washed by diethyl ether and vacuum-dried.\",Single-crystal X-ray diffraction,\"Single-crystal structure data was collected using a Bruker KAPPA APEX II diffractometer, APEX II CCD detector, and a Mo Kα source (λ = 0.71073 Å). APEX and Olex2 software was used for further refinement.\"\r\nhttps://doi.org/10.1021/acsnano.1c01134,Bis(rac-)methylbenzylammonium copper chloride,C16N2H242CuCl4,\"rac-MBA2CuCl4, (racemic-MBA)2CuCl4\",C8NH12,CuCl4,bis(rac-)methylbenzylaminium copper (II) chloride,2,single crystal,,,,,,,,\"(±)-α-methylbenzylamine (rac-MBA), ethanol, HCl, diethyl ether, copper(II) chloride dihydrate\",Single crystals of Bis(rac-)methylbenzylammonium copper chloride,\"The synthesis of a precursor solution, MBACl, was done by adding rac-MBA (5 mL) and ethanol (15 mL) to a round-bottom flask (250 mL), and stirring the mixture at 0 degrees Celsius. HCl (10 mL, 37%) was added, and the solution was stirred for two hours. Then, copper(II) chloride dihydrate (171 mg, 1 mmol), MBACl (315 mg, 2 mmol), and isopropyl alcohol were added to a vial under heat and stirred until all solids dissolved. The resulting dark green solution cooled to room temperature, while green single crystals of Bis(rac-)methylbenzylammonium copper chloride were precipitated. Crystals were washed by diethyl ether and vacuum-dried.\",Single-crystal X-ray diffraction,\"Single-crystal structure data was collected using a Bruker KAPPA APEX II diffractometer, APEX II CCD detector, and a Mo Kα source (λ = 0.71073 Å). APEX and Olex2 software was used for further refinement.\"\r\nhttps://doi.org/10.1021/cm2023696,Bis(phenethylammonium) copper chloride,CuCl4(C6H5CH2CH2NH3)2,\"CuCl4(PEA)2, bis(phenethylaminium) tetrachlorocuprate(II)\",C8H12N,\"CuCl4, Copper chloride\",bis(2-phenylethan-1-aminium) copper chloride,2,single crystal,,,,,,,,\"2-phenyl ethyl ammonium chloride , CuCl2·2H2O\",square brown plate-like crystals,Crystals were grown by slowly evaporating an aqueous equimolar solution of the precursors.,Single crystal X-ray diffraction,Frames were collected using a three-circle Bruker Apex diffractometer equipped with a CCD detector and operating with Mo Kα radiation\r\nhttps://doi.org/10.1021/jacs.0c00371,Piperidinium lead iodide,(C5H12N)PbI3,\"(piperidinium)PbI3, (PD)PbI3, piperidinium triiodoplumbate(II)\",C5H12N,\"PbI3, Lead iodide\",piperidinium lead (II) iodide,1,single crystal,,,,,,,,\"PbI2, piperidinium hydrochloride, HI (47 wt % in water)\",yellow prismatic crystals,\"PbI2 (0.92 g, 2 mmol) and piperidinium hydrochloride (0.63 g, 2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",Single crystal X-ray diffraction,The frames were recorded using a Rigaku Saturn 724+ CCD diffractometer with Mo Kα radiation (λ = 0.71073 Å).\r\nhttps://doi.org/10.1021/jacs.0c00371,3-fluoropiperidinium lead iodide,(C5H11FN)PbI3,\"(3-FPD)PbI3, (3- fluoropiperidinium)PbI3, 3-fluoropiperidinium triiodoplumbate(II)\",C5H11FN,\"PbI3, Lead iodide\",3-fluoropiperidinium lead (II) iodide,1,single crystal,,,,,,,,\"PbI2, 3-fluoropiperidinium hydrochloride, HI (47 wt % in water)\",yellow block-like crystals,\"PbI2 (0.92 g, 2 mmol) and 3-fluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",Thermogravimetric analysis (TGA),Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\r\nhttps://doi.org/10.1021/jacs.0c00371,4-fluoropiperidinium lead iodide,(C5H11FN)PbI3,\"(4-FPD)PbI3, (4-fluoropiperidinium)PbI3, 4-fluoropiperidinium triiodoplumbate(II)\",C5H11FN,\"PbI3, Lead iodide\",4-fluoropiperidinium lead (II) iodide,1,single crystal,,,,,,,,\"PbI2, 4-fluoropiperidinium hydrochloride, HI (47 wt % in water)\",yellow prismatic crystals,\"PbI2 (0.92 g, 2 mmol) and 4-fluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",Thermogravimetric analysis (TGA),Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\r\nhttps://doi.org/10.1021/jacs.0c00371,Piperidinium lead iodide,(C5H12N)PbI3,\"(piperidinium)PbI3, (PD)PbI3, piperidinium triiodoplumbate(II)\",C5H12N,\"PbI3, Lead iodide\",piperidinium lead (II) iodide,1,single crystal,,,,,,,,\"PbI2, piperidinium hydrochloride, HI (47 wt % in water)\",yellow prismatic crystals,\"PbI2 (0.92 g, 2 mmol) and piperidinium hydrochloride (0.63 g, 2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",Thermogravimetric analysis,Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\r\nhttps://doi.org/10.1021/jacs.0c00371,\"Bisdecakis(3,3-difluoropiperidinium) lead iodide\",C60H120F24N12Pb7I26,\"(3,3-difluoropiperidinium)12Pb7I26, (3,3-DFPD)12Pb7I26, bisdecakis(3,3-difluoropiperidinium) hexaicosiodo septaplumbate(II)\",C60H120F24N12,\"Pb7I26, Lead iodide\",\"bisdecakis(3,3-difluoropiperidinium) lead (II) iodide\",1,single crystal,,,,,,,,\"PbI2, 3,3-difluoropiperidinium hydrochloride, HI (47 wt % in water)\",yellow prismatic crystals,\"PbI2 (0.92 g, 2 mmol) and 3,3-difluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",Thermogravimetric analysis (TGA),Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\r\nhttps://doi.org/10.1021/jacs.0c00371,\"Bis(4,4-difluoropiperidinium) lead iodide\",(C5H10F2N)2PbI4,\"(4,4-difluoropiperidinium)2PbI4, (4,4-DFPD)2PbI4, bis(4,4-difluoropiperidinium) tetraiodoplumbate(II)\",C5H10F2N,\"PbI4, Lead iodide\",\"bis(4,4-difluoropiperidinium) lead (II) iodide\",2,single crystal,,,,,,,,\"PbI2, 4,4-difluoropiperidinium hydrochloride, HI (47 wt % in water)\",Red plate-like crystals,\"PbI2 (0.92 g, 2 mmol) and 4,4-difluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",Thermogravimetric analysis (TGA),Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\r\nhttps://doi.org/10.1021/jacs.1c00757,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,3,film,,DFT,Perdew-Burke-Ernzerhof,4x4x1,,JTH PAW,,\"DMF , 33 mg ml−1 MACl ,33 mg mL−1 MAPbBr3 , 889 mg mL−1 FAPbI3,\",FAPbI3,\"The FAPbI3 halide perovskites was synthesized via antisolvent quenching method. Specifically, 889 mg mL−1 FAPbI3, 33 mg mL−1 MAPbBr3, and  33 mg ml−1 MACl were dissolved in a mixed polar aprotic solvent between dimethylformamide (DMF) and dimethylsulfoxide (DMSO)  solvent. Diethyl ether (0.2 mL) was then added to the mixture followed by annealing at 150°C for 10 min.\",Photoluminescence Intensity,\"PL spectra of the perovskite film, FAPbI3, with treatment of IPA in relation to time (seconds).\"\r\nhttps://doi.org/10.1021/jacs.1c06841,S-β-methylphenethylammonium butylammonium lead bromide,C13H25N2PbBr4,[S-MePEA][C3A]PbBr4,C13H25N2,PbBr4,S-β-methylphenethylaminium butylaminium lead (II) bromide,2,film,,,,,,,,\"butylammonium bromide, S-β-methylphenethylamine, hydrobromic acid, PbBr2, γ-butyrolactone, acetonitrile, ethanol, diethyl ether\",Single crystals of S-β-methylphenethylammonium butylammonium lead bromide,\"First, S-β-methylphenethylamine was mixed with hydrobromic acid (47 wt % in water) with a ratio of 1:1.05 moles. This was done at 0° Celsius for 1 hour, before evaporation of the solvent. The remaining precipitate was dissolved and recrystallized in ethanol, then washed with diethyl ether and vacuum-dried overnight. This resulted in S-MePEABr.\r\n\r\nNext, S-MePEABr (21.6 mg), butylammonium bromide (15.4 mg), and PbBr2 (36.7 mg) were dissolved in a solvent of γ-butyrolactone (3 mL) and acetonitrile (9 mL) at a temperature of 80° Celsius. This solution cooled at a rate of 1° / hour down to 10° Celsius. The resulting crystals were clear and plate-like.\",UV-vis spectroscopy,\"Thin films of the material were prepared by spin-casting onto a glass substrate and annealing samples on a hot plate (100° Celsius, 10 mins). A Shimazu UV-2600 was used for measurements.\"\r\nhttps://doi.org/10.1021/jacs.1c06841,S-β-methylphenethylammonium butylammonium lead bromide,C13H25N2PbBr4,[S-MePEA][C3A]PbBr4,C13H25N2,PbBr4,S-β-methylphenethylaminium butylaminium lead (II) bromide,2,film,,,,,,,,\"butylammonium bromide, S-β-methylphenethylamine, hydrobromic acid, PbBr2, γ-butyrolactone, acetonitrile, ethanol, diethyl ether\",Single crystals of S-β-methylphenethylammonium butylammonium lead bromide,\"First, S-β-methylphenethylamine was mixed with hydrobromic acid (47 wt % in water) with a ratio of 1:1.05 moles. This was done at 0° Celsius for 1 hour, before evaporation of the solvent. The remaining precipitate was dissolved and recrystallized in ethanol, then washed with diethyl ether and vacuum-dried overnight. This resulted in S-MePEABr.\r\n\r\nNext, S-MePEABr (21.6 mg), butylammonium bromide (15.4 mg), and PbBr2 (36.7 mg) were dissolved in a solvent of γ-butyrolactone (3 mL) and acetonitrile (9 mL) at a temperature of 80° Celsius. This solution cooled at a rate of 1° / hour down to 10° Celsius. The resulting crystals were clear and plate-like.\",Circular dichroism spectroscopy,\"Thin films of the material were prepared by spin-casting onto a glass substrate and annealing samples on a hot plate (100° Celsius, 10 mins). A Chirascan V100 Plus-Spectropolarimeter was used for measurements. The exciton peak was divided by the absorbance to normalize the CD measurement.\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide,C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,,,,,,,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",Single-crystal X-ray diffraction (SC-XRD),\"A Rigaku XtaLAB Synergy-S diffractometer using Mo Kα radiation (λ = 0.71073 Å) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON’s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide,C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,,,,,,,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",Single-crystal X-ray diffraction (SC-XRD),\"A Rigaku XtaLAB Synergy-S diffractometer using Mo Kα radiation (λ = 0.71073 Å) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON’s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide,C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,,,,,,,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",Single-crystal X-ray diffraction (SC-XRD),\"A Rigaku XtaLAB Synergy-S diffractometer using Mo Kα radiation (λ = 0.71073 Å) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON’s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead bromide,C10H28N2PbBr4,(S-2-MeBA)2PbBr4,C5H14N,\"PbBr4, lead bromide\",S-2-methylbutylammonium lead (II) Bromide,2,single crystal,,,,,,,,\"S-2-MeBA, PbBr2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbBr4,\"Add (S-2-MeBA) (0.25 mmol) and PbBr2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbBr4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbBr4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbBr4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",Differential scanning calorimetry (DSC),\"A TA Discovery DSC 2500 was used to carry out low-temperature conventional differential scanning calorimetry (DSC) measurements. The instrument was under helium purge with a 5 K/min ramp from 298 K to 124 K and back to 298 K (with use of an LN2P cooler). Sample powder was loaded into a Tzero Hermetic aluminum pan, with temperature and enthalpy calibrated in advance.\r\n\r\nA similar instrument was used to perform high-temperature DSC measurements under nitrogen purge. The ramp rate was 5 K/min from 298 K to 603 K. An aluminum pan was hermetically sealed to contain samples.\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide (placeholder 485),C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium Lead Iodide,2,single crystal,,,,,,,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",Single-crystal X-ray diffraction (SC-XRD),\"A Rigaku XtaLAB Synergy-S diffractometer using Mo Kα radiation (λ = 0.71073 Å) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON’s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide (placeholder 486),C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,,,,,,,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",Single-crystal X-ray diffraction (SC-XRD),\"A Rigaku XtaLAB Synergy-S diffractometer using Mo Kα radiation (λ = 0.71073 Å) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON’s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide,C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,,,,,,,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",Differential scanning calorimetry (DSC),\"A TA Discovery DSC 2500 was used to carry out low-temperature conventional differential scanning calorimetry (DSC) measurements. The instrument was under helium purge with a 5 K/min ramp from 298 K to 124 K and back to 298 K (with use of an LN2P cooler). Sample powder was loaded into a Tzero Hermetic aluminum pan, with temperature and enthalpy calibrated in advance.\r\nA similar instrument was used to perform high-temperature DSC measurements under nitrogen purge. The ramp rate was 5 K/min from 298 K to 603 K. An aluminum pan was hermetically sealed to contain samples.\r\nGraph: \r\nCooling (5 K/min) of crystal with slow process is the upper graph. Notable points at 183 K and 188 K, where the structure transitions.\r\nHeating (5 K/min) of crystal with slow process is the lower graph. Notable points at 203 K and 213 K, where the structure transitions.\"\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide,C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,FHI-aims,,,3x4x4,\"relativistic atomic ZORA scalar, \r\ninclude spin orbit\",,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",,\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide,C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,FHI-aims,,,3x4x4,,\"relativistic atomic ZORA scalar, \r\ninclude spin orbit\",,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",,\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead iodide,C10H28N2PbI4,(S-2-MeBA)2PbI4,C5H14N,\"PbI4, lead iodide\",(S)-2-methylbutan-1-aminium lead (II) Iodide,2,single crystal,,,,3x4x4,\"relativistic atomic ZORA scalar, include spin orbit\",,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",,\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead bromide,C10H28N2PbBr4,(S-2-MeBA)2PbBr4,C5H14N,\"PbBr4, lead bromide\",S-2-methylbutylammonium lead (II) Bromide,2,single crystal,FHI-aims,density functional theory,\"HSE06 [α=0.25, ω=0.11 Å^(-1)]\",3x4x4,\"relativistic atomic ZORA scalar, include spin orbit\",FHI-aims intermediate settings,FHI-aims intermediate settings,\"S-2-MeBA, PbBr2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbBr4,\"Add (S-2-MeBA) (0.25 mmol) and PbBr2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbBr4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbBr4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbBr4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",,\r\nhttps://doi.org/10.1021/jacs.2c05574,S-2-methylbutylammonium lead bromide,C10H28N2PbBr4,(S-2-MeBA)2PbBr4,C5H14N,\"PbBr4, lead bromide\",S-2-methylbutylammonium lead (II) Bromide,2,single crystal,FHI-aims,density functional theory,\"HSE06 [α=0.25, ω=0.11 Å^(-1)]\",3x4x4,\"relativistic atomic ZORA scalar, include_spin_orbit\",FHI-aims intermediate settings,FHI-aims intermediate settings,\"S-2-MeBA, PbBr2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbBr4,\"Add (S-2-MeBA) (0.25 mmol) and PbBr2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbBr4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbBr4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbBr4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",,\r\nhttps://doi.org/10.1021/jacs.2c05574,Tributyl(methyl)phosphonium lead iodide,C13H30PPbI3,\"tributyl(methyl)phosphonium lead iodide, TPPbI3\",C13H30P,\"PbI3, lead iodide\",,2,single crystal,FHI-aims,,,3x4x4,\"relativistic atomic ZORA scalar, include spin orbit\",,,\"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",yellow flaky single crystals (S-2-MeBA)2PbI4,\"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",,\r\nhttps://doi.org/10.1021/jacs.5b00290,Propylammonium silsesquioxane copper chloride,C48H220Cl12Cu4N16O48Si32,\"CUPOSS, propane-1-aminium silsesquioxane dodecachloro tetracuprate(II)\",N/A,MX6,propane-1-aminium silsesquioxane copper chloride,3,single crystal,,,,,,,,\"A-POSS and CuCl2, PdCl2, PbCl2, or MnCl2\",\"CuPOSS, PdPOSS, PbPOSS, MnPOSS\",\"A- POSS and metal halides (CuCl3, PdCl2, PbCl3, and MnCl2) were either dissolved in water or hydrochloric acid and precipitated into ethanol or acetone solvents.\",Filtration,\"Yellow precipitation was collected via filtration (213 mg) after A-POSS (200 mg) and CuCl2 ( 120 mg) was dissolved in water and added to a solution of ethanol (60 mL) to yield CuPOSS. An orange precipitate was collected from the synthesis of A-POSS (264 mg) and PdCl2 (99mg) in water and a 2N HCl solution (1.85 mL) and then dropped into ethanol, which formed PdPOSS. A white precipitate was collected by dissolving A-POSS (311 mg) in a 2N HCl solution and PbCl2 (300 mg)  in an HCl solution that produced PbPOSS. Likewise, a white precipitate was collected from the synthesis of A-POSS (100 mg) and MnCl2 (67 mg) that was dissolved in water (0.384 mL) and added to an acetone solution (60 mL) for the production of MnPOSS.\"\r\nhttps://doi.org/10.1021/jacs.5b01025,Methylammonium Germanium Iodide,CH3NH3GeI3,\"MAGeI3, methylammonium triiodogermaniate(II)\",CH6N,\"GeI3, Germanium iodide\",methanaminium germanium iodide,3,single crystal,,,,,,,,\"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), methylamine (CH3NH2)\",\"deep red, elongated hexagonal plate-like CH3NH3GeI3 crystals\",\"GeI4 was synthesized from GeO2 and HI, and CH3NH3I was synthesized by reacting equimolar amounts of HI and CH3NH2.\r\nFor the synthesis of CH3NH3GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, CH3NH3I (159 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 °C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",Diffuse reflectance,\"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements.  BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1 - R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\nhttps://doi.org/10.1021/jacs.5b01025,Guanidinium Germanium Iodide,CH6N3GeI3,\"diaminomethanaminium triiodogermanate(II), C(NH2)3GeI3\",CH6N3,\"GeI3, Germanium iodide\",diaminomethanaminium germanium (II) iodide,1,single crystal,,,,,,,,\"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), guanidinium chloride (C(NH2)3Cl, 98%)\",\"yellow, elongated hexagonal tubular C(NH2)3GeI3 crystals\",\"GeI4 was synthesized from GeO2 and HI, and C(NH2)3I was synthesized by reacting ethanolic solutions of C(NH)(NH2)2 (prepared by neutralizing C(NH2)3Cl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI. For the synthesis of C(NH2)3GeI3 aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, C(NH2)3I (183 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 °C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",Diffuse reflectance,\"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1 - R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\nhttps://doi.org/10.1021/jacs.5b01025,Acetamidinium Germanium Iodide,C2H7N2GeI3,\"1-aminoethane-2-aminium triiodogermanate(II), CH3C(NH2)2GeI3\",C2H7N2,\"GeI3, Germanium iodide\",1-aminoethane-2-aminium germanium (II) iodide,3,single crystal,,,,,,,,\"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), acetamidinium chloride (CH3C(NH2)2Cl, 98%)\",\"yellow, elongated hexagonal tubular CH3C(NH2)2GeI3 crystals\",\"GeI4 was synthesized from GeO2 and HI, and CH3C(NH2)2I was synthesized by reacting ethanolic solutions of CH3C(NH)(NH2) (prepared by neutralizing CH3C(NH2)2Cl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI. \r\nFor the synthesis of CH3C(NH2)2GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, CH3C(NH2)2I (184 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 °C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",Diffuse reflectance,\"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1 - R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\nhttps://doi.org/10.1021/jacs.5b01025,Tris(methylammonium) Germanium Iodide,C3H10NGeI3,\"trimethanaminium triiodogermanate(II), (CH3)3NHGeI3, Trimethylammonium Germanium Iodide\",C3H10N,\"GeI3, Germanium iodide\",trimethanaminium germanium (II) iodide,1,single crystal,,,,,,,,\"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), trimethylammonium chloride ((CH3)3NHCl, 98%)\",\"pale yellow, elongated hexagonal tubular (CH3)3NHGeI3 crystals\",\"GeI4 was synthesized from GeO2 and HI, and (CH3)3NHI was synthesized by reacting ethanolic solutions of (CH3)3N (prepared by neutralizing (CH3)3NHCl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI. For the synthesis of (CH3)3NHGeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, (CH3)3NHI (187 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 °C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",Diffuse reflectance,\"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1 - R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\nhttps://doi.org/10.1021/jacs.5b01025,Isopropylammonium Germanium Iodide,C3H10NGeI3,\"Isopropanaminium triiodogermanate(II), (CH3)2C(H)NH3GeI3, Isopropylammonium Germanium Iodide\",C3H10N,\"GeI3, Germanium iodide\",Isopropanaminium germanium (II) iodide,1,single crystal,,,,,,,,\"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%),  Isopropylamine ((CH3)2C(H)NH2)\",\"pale yellow, elongated hexagonal tubular (CH3)2C(H)NH3GeI3 crystals\",\"GeI4 was synthesized from GeO2 and HI, and (CH3)2C(H)NH3I was synthesized by reacting equimolar amounts of HI and (CH3)2C(H)NH2. For the synthesis of (CH3)2C(H)NH3GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, (CH3)2C(H)NH3I (187 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 °C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",Diffuse reflectance,\"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1 - R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\nhttps://doi.org/10.1021/jacs.5b01025,Formamidinium germanium iodide,HC(NH2)2GeI3,\"diaminomethanide triiodogermanate(II), FAGeI3, HC(NH2)2GeI3, (NH2)2CHGeI3\",CH5N2,\"GeI3, Germanium iodide\",diaminomethanide germanium iodide,3,single crystal,,,,,,,,\"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), formamidinium chloride (HC(NH2)2Cl, 98%)\",\"orange, elongated hexagonal tubular CH3C(NH2)2GeI3 crystals\",\"GeI4 was synthesized from GeO2 and HI, and HC(NH2)2I was synthesized by reacting ethanolic solutions of HC(NH)(NH2) (prepared by neutralizing HC(NH2)2Cl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI.\r\nFor the synthesis of HC(NH2)2GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, HC(NH2)2I (172 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 °C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",Diffuse reflectance,\"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements.  BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1 - R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\nhttps://doi.org/10.1021/jacs.5b01025,Cesium Germanium Iodide,CsGeI3,*,none,CsGeI3,-,3,single crystal,,,,,,,,\"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), CsI (99.95%)\",Black truncated octahedral CsGeI3 crystals,\"GeI4 was synthesized from GeO2 and HI.\r\nFor the synthesis of CsGeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 °C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, CsI (260 mg, 1 mmol) was dissolved. After 5 minutes, the stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",Diffuse reflectance,\"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements.  BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: α/S = (1 - R)^2/2R, where R is the reflectance and α and S are the absorption and scattering coefficients, respectively.\"\r\nhttps://doi.org/10.1021/jacs.5b05404,Cesium lead bromide,CsPbBr3,\"Cesium tribromoplumbate(II), CsPbBr3\",None,\"PbBr3, Lead bromide\",Cesium lead(II) bromide,3,nanoform,,,,,,,,\"Cs2CO3 (99.9%, Aldrich), octadecene (ODE, 90%, Aldrich), oleic acid (OA, 90%, Aldrich), PbCl2 (99.999%, Aldrich), PbBr2 (99.999%, Aldrich), PbI2 (99%, Aldrich), oleylamine (OLA, Aldrich, 70%), hexane\",CsPbBr3 and CsPb13,\"A solution 5 mL of ODE and 0.18 mmol of PbX2 was degassed under vacuum and were then added to a mixture of OLA and OA, which was annealed at 120 degrees celsius. This solution was kept at a temperature of 150 degrees celsius as 0.6 mL of the inorganic-organic Cs-oleate solution was obtained. The reaction was then placed in a ice-water bath to isolate and purificate CsPbI3 and CsPbBr3 nanowires.\",Absorption Spectra,A Shimudzu UV-3010 PC UV-VIS-IR Scanning spectrophotometer equipped with a Shimadzu ISR-3100 was used to obtain the wavelength and absorbance of CsPbBr3.\r\nhttps://doi.org/10.1021/jacs.5b05404,Cesium lead iodide,CsPbI3,\"cesium lead iodide, cesium triiodoplumbate(II)\",None,CsPbI3,cesium lead(II) iodide,3,nanoform,,,,,,,,\"Cs2CO3 (99.9%, Aldrich), octadecene (ODE, 90%, Aldrich), oleic acid (OA, 90%, Aldrich), PbCl2 (99.999%, Aldrich), PbBr2 (99.999%, Aldrich), PbI2 (99%, Aldrich), oleylamine (OLA, Aldrich, 70%), hexane\",CsPbI3,\"A solution 5 mL of ODE and 0.18 mmol of PbX2 was degassed under vacuum and were then added to a mixture of OLA and OA, which was annealed at 120 degrees celsius. This solution was kept at a temperature of 150 degrees celsius as 0.6 mL of the inorganic-organic Cs-oleate solution was obtained. The reaction was then placed in a ice-water bath to isolate and purificate CsPbI3 and CsPbBr3 nanowires.\",Absorption Spectra,A Shimudzu UV-3010 PC UV-VIS-IR Scanning spectrophotometer equipped with a Shimadzu ISR-3100 was used to obtain the wavelength and absorbance of CsPbBr3.\r\nhttps://doi.org/10.1021/jacs.6b08175,Bis(phenylethylammonium) lead iodide,C16H24N2PbI4,\"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",C8H12N,\"PbI4, Lead iodide\",bis(2-phenylethane-1-aminium) lead(II) iodide,2,film,,,,,,,,\"Phenethylammonium lead iodide (PEALI) crystals, anhydrous acetonitrile (Acros Organics), sapphire substrates (Rayotek Scientific)\",Phenethylammonium lead iodide films,\"PEALI crystals are dissolved by sonication in anhydrous acetonitrile at a concentration of 15 mg/mL. The solution is filtered through a 0.2 µm PTFE syringe filter (Pall Corporation) and spun on cleaned sapphire substrates by ramping the spin rate over 2 s to 2500 rpm and spinning for 10 s. After spin-casting, the films are annealed for 10 min at 80 ˚C. The entire process is carried out in a nitrogen-filled glove box.\",UV-VIS Absorption,The absorption spectra measurements of PEALI thin films were obtained by using Agilent Cary 5000 spectrophotometer.\r\nhttps://doi.org/10.1021/jacs.7b04693,(3-pyrrolinium) cadmium bromide,(C4H8N)CdBr3,\"(3-pyrrolinium)CdBr3, (3-pyrrolinium) tribromocadmate(II)\",C4H8N,\"CdBr3, Cadmium bromide\",(3-pyrrolinium) cadmium bromide,1,single crystal,,,,,,,,\"CdBr2, pyrroline hydrobromide\",Colorless rod-like crystals,A molar mixture of the precursors was dissolved in water at room temperature. The crystals were grown in the solution by slow evaporation.,Single crystal X-ray diffraction,Rigaku Saturn 724+ CCD diffractometer with Mo–Kα radiation (λ = 0.71073 Å) were used to collect the diffraction data.\r\nhttps://doi.org/10.1021/ol9010745,\"thieno[3,2-b]thiophene\",C6H4S2,TbT,C6H4,S2,,3,single crystal,,,,,,,,,,,,\r\nhttps://doi.org/10.1038/ncomms16045,Formamidinium methylammonium lead iodide lead bromide,FA0.85MA0.15PbI2.55Br0.45,diaminomethanide methanaminium lead iodide lead bromide,\"CN2H3,CNH6\",PbI2.55PbBr0.45,diaminomethanide methanaminium lead iodide lead bromide,2,film,,,,,,,,\"formamidinium iodide, methylammonium bromide, PbI2, PbBr2\",thin film,\"By dissolving formamidinium acetate powder in a 2x molar excess of 57% acid (for FAI) or 48% hydrobromic acid (for MABr) formamidinium iodide (FAI) and methylammonium bromide (MABr) were synthesised. The solution was stirred for 10 minutes at 50° C. A yellow-white powder is formed upon drying at 100° C. This was washed with diethylether and recrystallized twice with ethanol, to form white needle-like crystals. It was dried overnight in a vacuum oven. To form FAPbI3 and FAPbBr3 precursor solutions, FAI and PbI2 or MABr and PbBr2 were dissolved in anhydrous N,N-dimethylformamide (DMF) in a 1:1 molar ratio, at 0.88M of each reagent, to give a 0.88M perovskite precursor solution. Mixtures were made of the FAPbI3 and FAPbBr3 solutions in the required ratios to form the FAPbI3yBr3(1-y) perovskite precursors. The perovskite precursor ink was prepared by dissolving FAI, MABr, PbI2 and PbBr2 (molar ratio of FAI:MABr:PbI2:PbBr2=0.85:0.15:2.55:0.45) in DMSO, and stirred at 60 °C for 2 h to form 0.25 M FA0.85MA0.15PbI2.55Br0.45 precursor ink.\",UV-Vis photoluminescence,\"Using a Shimadzu UV2600 spectrophotometer with a photometric integrating sphere, UV-Vis spectra were obtained.\"\r\nhttps://doi.org/10.1038/ncomms16045,Formamidinium methylammonium lead iodide lead bromide,FA0.85MA0.15PbI2.55Br0.45,diaminomethanide methanaminium lead iodide lead bromide,\"CN2H3,CNH6\",PbI2.55PbBr0.45,diaminomethanide methanaminium lead iodide lead bromide,2,film,,,,,,,,\"formamidinium iodide, methylammonium bromide, PbI2, PbBr2\",thin film,\"By dissolving formamidinium acetate powder in a 2x molar excess of 57% acid (for FAI) or 48% hydrobromic acid (for MABr) formamidinium iodide (FAI) and methylammonium bromide (MABr) were synthesised. The solution was stirred for 10 minutes at 50° C. A yellow-white powder is formed upon drying at 100° C. This was washed with diethylether and recrystallized twice with ethanol, to form white needle-like crystals. It was dried overnight in a vacuum oven. To form FAPbI3 and FAPbBr3 precursor solutions, FAI and PbI2 or MABr and PbBr2 were dissolved in anhydrous N,N-dimethylformamide (DMF) in a 1:1 molar ratio, at 0.88M of each reagent, to give a 0.88M perovskite precursor solution. Mixtures were made of the FAPbI3 and FAPbBr3 solutions in the required ratios to form the FAPbI3yBr3(1-y) perovskite precursors. The perovskite precursor ink was prepared by dissolving FAI, MABr, PbI2 and PbBr2 (molar ratio of FAI:MABr:PbI2:PbBr2=0.85:0.15:2.55:0.45) in DMSO, and stirred at 60 °C for 2 h to form 0.25 M FA0.85MA0.15PbI2.55Br0.45 precursor ink.\",UV-Vis Absorbtion,\"Using a Shimadzu UV2600 spectrophotometer with a photometric integrating sphere, UV-Vis spectra were obtained.\"\r\nhttps://doi.org/10.1038/s41467-018-07952-x,OITP,MAPbX3,trihalide perovskites,MA,PbX3,,3,film,,,,,,,,\"PbBr2 and MABr (1:1:1 molar ratio), dimethyl sulfoxide (0.5 M), ,\",OITP,OITP was produced by mixing a solution of PbBr2 and MABr in a 0.5 M concentration of dimethyl sulfoxide (DMSO). The solution was coated using SOC on an O2 substrate at 4000 rpm. The films were bathed in a chloroform solvent and heated at 100 °C until the crystals produced.,Spin-LED device,\"The spin-LED Method demonstrated an anode (MAPbBr3 spin-coated with LSMO) and a cathode (Al film coated on organic small molecules). A magnetic field was applied as spin-polarized and unpolarized electron was injected into the device, portraying measurements EL emissions and the voltage.\"\r\nhttps://doi.org/10.1038/s41467-020-18015-5,Cesium lead iodide bromide,CsPbBrI2,\"Cesium lead(II) bromide diiodide, cesium bromo diiodoplumbate\",none,CsPbBrI2,Cesium lead bromide diiodide,2,film,,,,,,,,\"PbI2, PbBr2, CsI, DMSO\",thin film,\"235.5 mg PbI2, 187 mg PbBr2, and 272 mg CsI were dissolved in DMSO to a final volume of 1 mL. This was stirred overnight at room temperature.\",UV-Vis spectroscopy,UV–Vis spectra were collected using a Cary 500 UV–Vis–NIR spectrophotometer in air ambient environments.\r\nhttps://doi.org/10.1038/s41467-020-18015-5,Cesium lead iodide bromide,CsPbBrI2,\"Cesium lead(II) bromide diiodide, cesium bromo diiodoplumbate\",none,CsPbBrI2,Cesium lead bromide diiodide,3,film,,,,,,,,\"Pb(DDTC)2, PbI2, PbBr2, CsI, DMSO\",thin film,\"Synthesis of Pb(DDTC)2 by addition of 20.0 M NaDDTC·3H2O\r\naqueous solution to Pb(NO3)2 aqueous solution (10.0 M) during constant stirring at room temperature. After 30 minutes, filtering of yellow precipitate and washing four times with water, drying at 60°C in oven. Dissolution of 30.22 mg Pb(DDTC)2 into 2.0 mL DMSO\r\nsolution to result in Pb(DDTC)2-DMSO solution (0.03 M).  235.5 mg PbI2, 187\r\nmg PbBr2, and 272 mg CsI were dissolved in DMSO and Pb(DDTC)2-DMSO\r\nmixed solution to a final volume of 1 mL with desired Pb(DDTC)2 concentration. This was stirred overnight at room temperature. Then thin films were deposited onto glass substrates.\",Steady-state photoluminescence,The steady-state PL were acquired by Fluorolog-3-p spectrophotometer in air at room temperature. PL excitation wavelength was 380 nm.\r\nhttps://doi.org/10.1039/C7EE03113K,Acetylacetonate methylammonium iodide gallium,C16H28GaINO6,GaAA3-MAI,C16H28,GaINO6,4-oxopent-2-en-2-olate methanaminium gallium iodide,0,single crystal,,,,,,,,,,,Single crystal X-ray diffraction,Frames were collected using Gemini S Ultra CCD area-detector diffractometer.\r\nhttps://doi.org/10.1039/C7EE03113K,Acetylacetonate gallium,C15H21GaO6,GaAA3,C15H21,GaO6,4-oxopent-2-en-2-olate gallium,3,single crystal,,,,,,,,acetylacetonate solvent,GaAA3,GaAA3 was synthesized by 100 mg GaAA3 in 1ml acetylacetonate solvent. The solution was placed at  100 degrees celsius and stirred until single crystals of the product was produced.,,\r\nhttps://doi.org/10.1039/C7TA04690A,Cesium silver indium chloride,Cs2InAgCl6,Dicesium trichloroargentate(I) trichloroindiate(III),None,InAgCl6,,2,powder,,,,,,,,\"CsCl, AgCl, InCl3, HCl\",Cs2AgInCl6 microcrystals,\"In 0.5 ml HCl, 2.4 mmol CsCl, 1.2 mmol AgCl and 1.2 mmol InCl3 were combined and heated at 423 K for 12 h. This resulted in a white powder which was filtered and washed with ethanol and dried under reduced pressure. If the heating time is prolonged to 72 h, it is possible to obtain larger crystals.\",Powder X-ray diffraction,\"Powder X-ray diffraction using D8 Advance diffractometer (Bruker Corporation), Cu Kα radiation, wavelength of 1.5406 Å\"\r\nhttps://doi.org/10.1039/D1TA03325E,[(NDIC2)2Pb5I14(DMF)2]·4DMF,C13.5H19.5I3.5N3.5O3.50Pb1.25,\"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone triiodoplumbate(II)\",C13.50H19.5,I3.5N3.5O3.50Pb1.25,\"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone iodide\",1,single crystal,,,,,,,,\"NDIC2, Pb2I6, DMF,\",[(NDIC2)2Pb5I14(DMF)2]·4DMF,,Absorption Spectrum,NDIC2-I2 was dissolved in DMF and the solution-phase optical absorption spectrum was measured.\r\nhttps://doi.org/10.1039/D1TA03325E,[(NDIC2)2Pb5I14(DMF)2]·4DMF,C13.5H19.5I3.5N3.5O3.50Pb1.25,\"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone triiodoplumbate(II)\",C13.50H19.5,I3.5N3.5O3.50Pb1.25,\"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone iodide\",1,single crystal,,,,,,,,,,,Temperature-dependent PL emission spectra,\"The organic-inorganic compounds, (NDIC2)Pb2I , PL emission spectra was measured at 5 different temperatures in kelvin (e.g 5 K, 10 K, 20 K, 40 K, 80 K). After measuring the intensities at those wavelengths, they were analyzed on a intensity vs temperature graph.\"\r\nhttps://doi.org/10.1126/science.aay7044,Formamidinium lead iodide:1.9%MDACl2,CH5N2PbI3:1.9%CH8N2Cl2,\"FAPbI3:MDACl2, FAPbI3:1.9%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\"CH5N2,CH8N2\",PbI3:Cl-,Imidoformamidinium lead iodide: methylenediammonium chloride,2,film,,,,,,,,\"formamidine acetate salt, hydroiodic acid, lead iodide\",thin film,\"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60°C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120°C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150°C. A small amount of MADCl2 was incorporated.\",UV-Vis spectroscopy,The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\r\nhttps://doi.org/10.1126/science.aay7044,Formamidinium lead iodide:1.9%MDACl2,CH5N2PbI3:1.9%CH8N2Cl2,\"FAPbI3:MDACl2, FAPbI3:1.9%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\"CH5N2,CH8N2\",PbI3:Cl-,Imidoformamidinium lead iodide: methylenediammonium chloride,2,film,,,,,,,,\"formamidine acetate salt, hydroiodic acid, lead iodide\",thin film,\"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60°C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120°C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150°C. A small amount of MADCl2 was incorporated.\",UV-Vis spectroscopy,The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\r\nhttps://doi.org/10.1126/science.aay7044,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,2,film,,,,,,,,\"formamidine acetate salt, hydroiodic acid, lead iodide\",thin film,\"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60°C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120°C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150°C.\",UV-Vis spectroscopy,The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\r\nhttps://doi.org/10.1126/science.aay7044,Formamidinium lead iodide,CH5N2PbI3,\"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",CH5N2,\"PbI3, Lead iodide\",Imidoformamidinium lead(II) iodide,2,film,,,,,,,,\"formamidine acetate salt, hydroiodic acid, lead iodide\",thin film,\"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60°C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120°C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150°C.\",UV-Vis spectroscopy,\"Steady-state photoluminescence (PL) spectra were measured using a commercial time-correlated single photon counting (TCSPC) setup (FluoTime 300, PicoQuant GmbH) equipped with PMA-C-192-M detector, high-resolution excitation monochromators.\"\r\nhttps://doi.org/10.1126/science.aay7044,Formamidinium lead iodide:3.8%MDACl2,CH5N2PbI3:3.8%CH8N2Cl2,\"FAPbI3:MDACl2, FAPbI3:3.8%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\"CH5N2,CH8N2\",PbI3:Cl-,Imidoformamidinium lead iodide: methylenediammonium chloride,2,film,,,,,,,,\"formamidine acetate salt, hydroiodic acid, lead iodide\",thin film,\"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60°C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120°C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150°C. A small amount of MADCl2 was incorporated.\",UV-Vis absorption,The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\r\nhttps://doi.org/10.1126/science.aay7044,Formamidinium lead iodide:5.7%MDACl2,CH5N2PbI3:5.7%CH8N2Cl2,\"FAPbI3:MDACl2, FAPbI3:5.7%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\"CH5N2,CH8N2\",PbI3:Cl-,Imidoformamidinium lead iodide: methylenediammonium chloride,2,film,,,,,,,,\"formamidine acetate, hydroiodic acid (HI, 57 wt% in water), lead iodide, 2-methoxyethanol (anhydrous 99.8%)\",thin film,\"By reaction of 20 mg of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60°C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was synthesized in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120°C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150°C. A small amount of MADCl2 was incorporated.\",UV-Vis spectroscopy,The absorption spectrum was measured using Shimadzu UV-2600.\r\n"
  },
  {
    "path": "dataset/Crystalline organic-inorganic compounds/dataset_info_json_intent.json",
    "content": "[\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 6,\n        \"id\": 12,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            384\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin-film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 7,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            380\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 8,\n        \"id\": 13,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead chloride\",\n        \"formula\": \"C14H20N2PbCl4\",\n        \"group\": \"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            385\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 9,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            381\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 10,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            383\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 11,\n        \"id\": 2,\n        \"compound_name\": \"Bis(phenylethylammonium) lead chloride\",\n        \"formula\": \"C16H24N2PbCl4\",\n        \"group\": \"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PEA)2PbCl4, (C8H12N)2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            377\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 12,\n        \"id\": 7,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead bromide\",\n        \"formula\": \"C22H24N2PbBr4\",\n        \"group\": \"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"NMA2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            379\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NMA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin-film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He\\u2212Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 13,\n        \"id\": 14,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead chloride\",\n        \"formula\": \"C22H24N2PbCl4\",\n        \"group\": \"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            386\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NMA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He\\u2212Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 14,\n        \"id\": 6,\n        \"compound_name\": \"Bis(2-(2-naphthyl)ethanammonium) lead iodide\",\n        \"formula\": \"C24H28N2PbI4\",\n        \"group\": \"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(2-naphthyl)ethane-1-aminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"NEA2PbI4, (C24H28N2)PbI4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            378\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NEA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystal into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He\\u2212Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pn\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 15,\n        \"id\": 10,\n        \"compound_name\": \"Bis(2-(2-naphtyl)ethanammonium) lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            382\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NEA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystal into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He\\u2212Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 16,\n        \"id\": 15,\n        \"compound_name\": \"Bis(Butylammonium) germanium iodide\",\n        \"formula\": \"C8H24N2GeI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodogermanate(II), (C4H9NH3)2GeI4, (C4H12N)2GeI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"GeI4, Germanium iodide\",\n        \"iupac\": \"bis(butane-1-aminium) germanium(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            387\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"GeI4, HI, H3PO2, C4H9NH2\",\n        \"synthesis_product\": \"Bright orange sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.709 g (1.22 mmol) of GeI4 in 50 mL 3 M HI solution at 80 \\u00b0C. Raise the temperature of the solution to 98 \\u00b0C and add 4 mL concentrated (50 wt %) aqueous H3PO2 solution. Allow the reduction of GeI4 to GeI2 to proceed for approximately 4 h, then add a solution of 0.491 g (2.44 mmol) of (C4H9NH2).HI in 3 mL of concentrated (57 wt %) aqueous HI, producing a yellow solution. Allow the resulting solution to sit at 80 \\u00b0C in flowing argon until approximately 50% of the solution had evaporated and then slowly (2-5 \\u00b0C/h) cool to -10 \\u00b0C. Filter out the crystals under flowing argon and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pcmn\",\n        \"extraction_method\": \"Engauge Digitizer, Figure 5\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 17,\n        \"id\": 16,\n        \"compound_name\": \"Bis(Butylammonium) tin iodide\",\n        \"formula\": \"C8H24N2SnI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodostannate(II), (C4H9NH3)2SnI4, (C4H12N)2SnI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            388\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"SnI2, HI, C4H9NH2\",\n        \"synthesis_product\": \"Dark red sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.481 g (1.29 mmol) of SnI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 \\u00b0C. In a separate tube, dissolve 2.58 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 \\u00b0C/h from 90 to -10 \\u00b0C, filter the crystals formed under argon or nitrogen and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer, Figure 5\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 18,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            389\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C4H9NH2\",\n        \"synthesis_product\": \"Orange-yellow sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.534 g (1.16 mmol) of PbI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 \\u00b0C. In a separate tube, dissolve 2.32 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 \\u00b0C/h from 90 to -10 \\u00b0C, filter the crystals formed under argon or nitrogen and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer, Figure 5\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C5CP02605A\",\n        \"dataset_ID\": 22,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Characterization of an abnormal photoluminescence behavior upon crystal-phase transition of perovskite CH3NH3PbI3\",\n        \"journal\": \"Physical Chemistry Chemical Physics\",\n        \"vol\": \"17\",\n        \"pages_start\": \"16405\",\n        \"pages_end\": \"16411\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 \\u00b0C for 2 h. Evaporate solvents at 50 \\u00b0C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 \\u00b0C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Steady-state and time-resolved PL spectra were measured using an Edinburgh FLS920 spectroscopy system using laser excitation at 405 nm. PL peak is due to near-band edge transition. [Results and discussion paragraph 3; Fig. 2(b) Peak_OI]\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"PL peak vs temperature\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 106,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"tight\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 107,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"PBE with Tkatchenko-Scheffler van der Waals correction\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"tight\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 108,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"PBE with many-body dispersion (range-separated MBD@rsSCS)\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"tight\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b00781\",\n        \"dataset_ID\": 126,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Free Carriers versus Excitons in CH3NH3PbI3 Perovskite Thin Films at Low Temperatures: Charge Transfer from the Orthorhombic Phase to the Tetragonal Phase\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"7\",\n        \"pages_start\": \"2316\",\n        \"pages_end\": \"2321\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbI2, dimethylformamide, quartz substrate, CH3NH3I (in 0.06 M 2-propanol)\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"Deposit 1.0 M solution of PbI2 (L0279 for the perovskite precursor, Tokyo Chemical Industry Co. Ltd., Japan) in dehydrated dimethylformamide at 70 \\u00b0C on a quartz substrate by spin-coating (slope 5 s, 6500 rpm, 5 s, slope 5 s). Anneal the resulting yellow film on a hot plate at 70 \\u00b0C for 1 h. Dip the PbI2 film in a 0.06 M 2-propanol solution of CH3NH3I (Tokyo Chemical Industry Co., Ltd., Japan) for 40 s. Anneal the formed perovskite film on a hot plate at 70 \\u00b0C for 1 h. Keep the samples in vacuum at RT for several days before the optical measurements; this process helps to reduce significantly the unreacted PbI2 and subsequently improves the quality of thin film samples.\",\n        \"experimental_method\": \"Optical-transient absorption\",\n        \"experimental_description\": \"Optical transient absorption peak attributed to near-band-edge photocarriers, TA measurements were based on a Yb:KGW regenerative amplified laser (pulse duration: \\u223c300 fs; repetition rate: 50\\u2212100 kHz). Refer to Page 2318 paragraph 1; Figure 2. (a) O-TA.\",\n        \"physical_property\": \"15.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Absorption peak at 15 K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201606405\",\n        \"dataset_ID\": 128,\n        \"id\": 41,\n        \"compound_name\": \"Formamidinium lead bromide\",\n        \"formula\": \"CH5N2PbBr3\",\n        \"group\": \"Methanimidamide tribromoplumbate(II), FAPBr3, FAPBr, (FA)PbBr3 HC(NH2)2PbBr3, (NH2)2CHPbBr3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Imidoformamidinium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Perovskite Light-Emitting Diodes Based on Perovskite Nanocrystals with Organic\\u2013Inorganic Mixed Cations\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"29\",\n        \"pages_start\": \"1606405\",\n        \"pages_end\": \"1606405\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"FABr, PbBr2, CsBr, toluene, THF\",\n        \"synthesis_product\": \"Thin film/Solution\",\n        \"synthesis_description\": \"Add mixture of precursors drop-wise into the toluene solution for NC formation, and centrifuge the final product. Disperse NCs in THF with a concentration of 20 mg mL\\u22121. Refer to Page 2 paragraph 4; Figure 2(a).\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Instrumental details not provided. Refer to Page 3 paragraph 2; Figure 2(d); SI Table S2.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 129,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HCl, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"MAPbCl3 single crystal ~1mm, colorless\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbCl3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 37 wt% HCl aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add an excess of HCl to prevent the co-precipitation of PbCl2 in agreement with previous work [2], along with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days. Refer to Page 9299 Section 2.1 Synthesis; Figure 2.\",\n        \"experimental_method\": \"UV-Vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"UV-Visible-NIR spectrophotometer (Shimadzu UV-3600) with integrating sphere attachment (ISR-3100) operating in the 300\\u20131500 nm region. Highly refined barium sulfate powder (Wako, pure) was used as a reflectance standard. Optical absorption coefficient was determined according to the Kubelka\\u2013Munk equation. In this manner, optical band gaps for the perovskites were determined. Refer to Page 9300 Section 3.1 Paragraph 3; Figure 3,4.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Absorption peak at r.t.p.\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 131,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HBr, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"MAPbBr3 single crystal ~0.1mm, bright red/orange\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbBr3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 48 wt% HBr aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add another 2 ml of HBr solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days. Refer to Page 9299 Section 2.1 Synthesis; Figure 1.\",\n        \"experimental_method\": \"UV-Vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"UV-Visible-NIR spectrophotometer (Shimadzu UV-3600) with integrating sphere attachment (ISR-3100) operating in the 300\\u20131500 nm region. Highly refined barium sulfate powder (Wako, pure) was used as a reflectance standard. Optical absorption coefficient was determined according to the Kubelka\\u2013Munk equation. In this manner, optical band gaps for the perovskites were determined. Refer to Page 9300 Section 3.1 Paragraph 3; Figure 3,4.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Absorption peak at r.t.p.\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 132,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"MAPbI3 Single crystal\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days. Refer to Page 9299 Section 2.1 Synthesis.\",\n        \"experimental_method\": \"UV-Vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"UV-Visible-NIR spectrophotometer (Shimadzu UV-3600) with integrating sphere attachment (ISR-3100) operating in the 300\\u20131500 nm region. Highly refined barium sulfate powder (Wako, pure) was used as a reflectance standard. Optical absorption coefficient was determined according to the Kubelka\\u2013Munk equation. In this manner, optical band gaps for the perovskites were determined. Refer to Page 9300 Section 3.1 Paragraph 3; Figure 3,4.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"Absorption peak at r.t.p.\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C5CP02605A\",\n        \"dataset_ID\": 134,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Characterization of an abnormal photoluminescence behavior upon crystal-phase transition of perovskite CH3NH3PbI3\",\n        \"journal\": \"Physical Chemistry Chemical Physics\",\n        \"vol\": \"17\",\n        \"pages_start\": \"16405\",\n        \"pages_end\": \"16411\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 \\u00b0C for 2 h. Evaporate solvents at 50 \\u00b0C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 \\u00b0C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Steady-state and time-resolved PL spectra were measured using an Edinburgh FLS920 spectroscopy system using laser excitation at 405 nm. PL peak is due to the near-band-edge transition. Refer to Results and discussion paragraph 2; Fig. 2(a) Peak_T.\",\n        \"physical_property\": \"405.0\",\n        \"unit\": \"nm\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"PL peak vs temperature\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b00781\",\n        \"dataset_ID\": 135,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Free Carriers versus Excitons in CH3NH3PbI3 Perovskite Thin Films at Low Temperatures: Charge Transfer from the Orthorhombic Phase to the Tetragonal Phase\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"7\",\n        \"pages_start\": \"2316\",\n        \"pages_end\": \"2321\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbI2, dimethylformamide, quartz substrate, CH3NH3I (in 0.06 M 2-propanol)\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"Deposit 1.0 M solution of PbI2 (L0279 for the perovskite precursor, Tokyo Chemical Industry Co. Ltd., Japan) in dehydrated dimethylformamide at 70 \\u00b0C on a quartz substrate by spin-coating (slope 5 s, 6500 rpm, 5 s, slope 5 s). Anneal the resulting yellow film on a hot plate at 70 \\u00b0C for 1 h. Dip the PbI2 film in a 0.06 M 2-propanol solution of CH3NH3I (Tokyo Chemical Industry Co., Ltd., Japan) for 40 s. Anneal the formed perovskite film on a hot plate at 70 \\u00b0C for 1 h. Keep the samples in vacuum at RT for several days before the optical measurements; this process helps to reduce significantly the unreacted PbI2 and subsequently improves the quality of thin film samples.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL measurements were based on a Yb:KGW regenerative amplified laser (pulse duration: \\u223c300 fs; repetition rate: 50\\u2212100 kHz) with 1.8 eV photoexcitation. O-PL peak emerged under strong fluences. Refer to Page 2317 paragraph 3; Figure 1. (a) O-PL.\",\n        \"physical_property\": \"15.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b00781\",\n        \"dataset_ID\": 136,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Free Carriers versus Excitons in CH3NH3PbI3 Perovskite Thin Films at Low Temperatures: Charge Transfer from the Orthorhombic Phase to the Tetragonal Phase\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"7\",\n        \"pages_start\": \"2316\",\n        \"pages_end\": \"2321\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbI2, dimethylformamide, quartz substrate, CH3NH3I (in 0.06 M 2-propanol)\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"Deposit 1.0 M solution of PbI2 (L0279 for the perovskite precursor, Tokyo Chemical Industry Co. Ltd., Japan) in dehydrated dimethylformamide at 70 \\u00b0C on a quartz substrate by spin-coating (slope 5 s, 6500 rpm, 5 s, slope 5 s). Anneal the resulting yellow film on a hot plate at 70 \\u00b0C for 1 h. Dip the PbI2 film in a 0.06 M 2-propanol solution of CH3NH3I (Tokyo Chemical Industry Co., Ltd., Japan) for 40 s. Anneal the formed perovskite film on a hot plate at 70 \\u00b0C for 1 h. Keep the samples in vacuum at RT for several days before the optical measurements; this process helps to reduce significantly the unreacted PbI2 and subsequently improves the quality of thin film samples.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL measurements were based on a Yb:KGW regenerative amplified laser (pulse duration: \\u223c300 fs; repetition rate: 50\\u2212100 kHz) with 1.8 eV photoexcitation. T-PL peak visible at low fluences. Refer to Page 2317 paragraph 3; Figure 1. (a) T-PL.\",\n        \"physical_property\": \"15.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Photoluminescence peak at 15K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ee43822h\",\n        \"dataset_ID\": 137,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1958\n        ],\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formamidinium lead trihalide: a broadly tunable perovskite for efficient planar heterojunction solar cells\",\n        \"journal\": \"Energy & Environmental Science\",\n        \"vol\": \"7\",\n        \"pages_start\": \"982\",\n        \"pages_end\": \"988\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"Methylamine (CH3NH2), (HI) 57 wt % in water, PbI2\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"React ~24 mL methylamine (CH3NH2) solution 33 wt% in absolute ethanol with ~10 mL hydroiodic acid (HI) 57 wt % in water with excess methylamine under nitrogen atmosphere in ~100 mL ethanol at room temperature. Crystallize methylammonium iodide (CH3NH3I) using a rotary evaporator to form a white colored powder. Prepare MAPbI3 precursor by dissolving equimolar amounts of methylammonium iodide and PbI2 in DMF at 0.88M in a nitrogen-filled glovebox. Spin-coat film at 2000rpm and anneal at 100 \\u00b0C for 5 minutes in the glovebox.\",\n        \"experimental_method\": \"Optical absorption\",\n        \"experimental_description\": \"Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere. Estimated band gap was determined from the extrapolation of the linear region to the energy-axis intercept in the direct bandgap Tauc plot.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201606405\",\n        \"dataset_ID\": 138,\n        \"id\": 489,\n        \"compound_name\": \"Formamidinium(1-x) cesium(x) lead bromide: x = 0.6\",\n        \"formula\": \"FA(0.4)Cs(0.6)PbBr3\",\n        \"group\": \"Methanimidamide cesium tribromoplumbate(II), FA0.4Cs0.6PBr3, FAPBr, (FA)CsPbBr3 HC(NH2)2CsPbBr3, (NH2)2CHPbBr3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"Cs0.6PbBr3, Lead bromide\",\n        \"iupac\": \"Imidoformamidinium cesium lead(II) bromide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            41,\n            326\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Perovskite Light-Emitting Diodes Based on Perovskite Nanocrystals with Organic\\u2013Inorganic Mixed Cations\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"29\",\n        \"pages_start\": \"1606405\",\n        \"pages_end\": \"1606405\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"FABr, PbBr2, CsBr, toluene, THF\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"Add mixture of precursors drop-wise into the toluene solution for NC formation, and centrifuge the final product. Disperse NCs in THF with a concentration of 20 mg mL\\u22121. Refer to Page 2 paragraph 4; Figure 2(a).\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Instrumental details not provided. Refer to Page 3 paragraph 2; Figure 2(e); SI Table S2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Photoluminescence peak\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505002\",\n        \"dataset_ID\": 139,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Single Crystal Formamidinium Lead Iodide (FAPbI3): Insight into the Structural, Optical, and Electrical Properties\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2253\",\n        \"pages_end\": \"2258\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Pb(ac) 2\\u00b73H2O, 99%), fomamidine acetate salt (FAac, 99%), lead iodide (PbI2 , 99.999%), hydriodic acid (HI) (57% w/w aq. soln., stabilized with H3PO2), and gamma-butyrolactone (GBL, 99%) were purchased from Sigma-Aldrich\",\n        \"synthesis_product\": \"FAPbI3 Single-crystal 5 mm yellow\",\n        \"synthesis_description\": \"Synthesis of Seed Crystal of FAPbI3: \\r\\nDissolve 2.5 g Pb(ac)2 \\u00b73H2O in 15 mL of HI in a 100 mL flask in a 105 \\u00b0C oil bath. Add 1.5 mL HI solution and 0.7 g of FAac to the mixed acid solution. Decrease the temperature of the mixed solution to 70 \\u00b0C; maintain temperature for 6 h for the precipitation of seed crystal FAPbI3 (\\u22481 mm in size). Wash crystals with diethyl ether and dry in vacuum. \\r\\n\\r\\nSynthesis of Single Crystal FAPbI3: \\r\\nDissolve 1.0 M solution containing PbI2 and FAI (1:1) was in GBL at 60 \\u00b0C overnight. Filter the solution using PTFE filter with 0.2 \\u00b5m pore size. Place seed crystals into this GBL solution in oil bath \\u2248100\\u2013105 \\u00b0C for 3 h to grow larger crystals. Replace with fresh precursor to obtain an even larger crystal. Repeat this process three times to obtain a large single crystal FAPbI3 in alpha phase. The crystals turn to the yellow delta-phase in 10 days.\\r\\n\\r\\nRefer to Page 2257 Experimental section.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"NKT SuperK Extreme laser with an excitation of 475 nm and New Focus Si fW detector. Refer to SI Figure S5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"Photoluminescence peak\",\n        \"space_group\": \"P6(3)mc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505002\",\n        \"dataset_ID\": 140,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Single Crystal Formamidinium Lead Iodide (FAPbI3): Insight into the Structural, Optical, and Electrical Properties\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2253\",\n        \"pages_end\": \"2258\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Pb(ac) 2\\u00b73H2O, 99%), fomamidine acetate salt (FAac, 99%), lead iodide (PbI2 , 99.999%), hydriodic acid (HI) (57% w/w aq. soln., stabilized with H3PO2), and gamma-butyrolactone (GBL, 99%) were purchased from Sigma-Aldrich\",\n        \"synthesis_product\": \"FAPbI3 Single-crystal 5 mm black\",\n        \"synthesis_description\": \"Synthesis of Seed Crystal of FAPbI3: Dissolve 2.5 g Pb(ac)2 \\u00b73H2O in 15 mL of HI in a 100 mL flask in a 105 \\u00b0C oil bath. Add 1.5 mL HI solution and 0.7 g of FAac to the mixed acid solution. Decrease the temperature of the mixed solution to 70 \\u00b0C; maintain temperature for 6 h for the precipitation of seed crystal FAPbI3 (\\u22481 mm in size). Wash crystals with diethyl ether and dry in vacuum. Synthesis of Single Crystal FAPbI3: Dissolve 1.0 M solution containing PbI2 and FAI (1:1) was in GBL at 60 \\u00b0C overnight. Filter the solution using PTFE filter with 0.2 \\u00b5m pore size. Place seed crystals into this GBL solution in oil bath \\u2248100\\u2013105 \\u00b0C for 3 h to grow larger crystals. Replace with fresh precursor to obtain an even larger crystal. Repeat this process three times to obtain a large single crystal FAPbI3 in alpha phase.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Horiba Jobin Yvon system. Refer to Page 2255 paragraph 1, Figure 2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"Photoluminescence peak\",\n        \"space_group\": \"P3m1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 144,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I [from synthesis], SnI2 [from synthesis], distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black MASnI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, elongated, rhombic dodecahedral (12 faces) crystals of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 146,\n        \"id\": 44,\n        \"compound_name\": \"Formamidinium tin iodide\",\n        \"formula\": \"CH5N2SnI3\",\n        \"group\": \"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"Imidoformamidinium tin (II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HC(NH2)2I [from synthesis], SnI2 [from synthesis], distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black FASnI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black rhombic dodecahedral crystals (12 faces) of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 147,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I [from syn], PbI2 [from syn], distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, rhombic dodecahedral crystals (12 faces) of the title compound precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"I4cm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 148,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HC(NH2)2I, PbI2, distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black FAPbI3 Crystals (\\u03b1 phase)\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Stop stirring and leave solution to evaporate at 100 \\u00b0C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. After standing for 2-3 h at 100 \\u00b0C, under a nitrogen atmosphere, set temperature to 80 \\u00b0C for a further 2-3 h. Repeat the previous step for two more times to reach 60 \\u00b0C and 40 \\u00b0C at which point the solution was left to come to room temperature by powering off the hotplate. The crystals were collected by filtration and washed with anhydrous EtOH.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"Estimate of band gap at r.t.p.\",\n        \"space_group\": \"P3m1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 149,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I, SnI2\",\n        \"synthesis_product\": \"Black MASnI3 Solid\",\n        \"synthesis_description\": \"Load equimolar amounts of SnI2 and MAI in a 9mm pyrex tube. Shake materials mechanically to ensure a homogenous mixture. Place tube on a sealing line evacuated to 10-4 mbar and flame sealed. Immerse tube on a sand bath standing at 200 \\u00b0C, such that the mixture of solids was heated homogeneously. Maintain 4/5 of the tube outside the bath at room temperature. Leave solids in the bath for 2 h to form a homogeneous black solid. The Sn containing solids are air sensitive. No obvious color changes are observed.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"Estimate of band gap at r.t.p.\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 150,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I, PbI2\",\n        \"synthesis_product\": \"Black MAPbI3 Solid\",\n        \"synthesis_description\": \"Load equimolar amounts of PbI2 and MAI in a 9mm pyrex tube. Shake materials mechanically to ensure a homogenous mixture. Place the tube on a sealing line evacuated to 10-4 mbar and flame sealed. Immerse tube on a sand bath standing at 200 \\u00b0C, such that the mixture of solids was heated homogeneously. Maintain 4/5 of the tube outside the bath at room temperature. Leave solids in the bath for 2 h to form a homogeneous black solid.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 151,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I, SnI2\",\n        \"synthesis_product\": \"Black MASnI3 Ingot\",\n        \"synthesis_description\": \"Load equimolar amounts of SnI2 and MAI in a 15mm pyrex test tube. Shake materials mechanically to ensure a homogenous mixture. Immerse in a sand bath standing at 350 \\u00b0C under a gentle flow of nitrogen. The reaction proceeds within 0.5-1 min. The formation of a homogeneous black melt signals the end of the reaction. Upon melting the tube was removed from the bath and left to cool in air, usually producing a shiny black ingot.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 152,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I, PbI2\",\n        \"synthesis_product\": \"Black MAPbI3 Ingot\",\n        \"synthesis_description\": \"Load equimolar amounts of PbI2 and MAI in a 15mm pyrex test tube. Shake materials mechanically to ensure a homogenous mixture. Immerse in a sand bath standing at 350 \\u00b0C under a gentle flow of nitrogen. The reaction proceeds within 0.5-1 min. Pb-containing solids decompose on prolonged heating (> 3 min) or by raising the temperature above 400 \\u00b0C, through evolution of I2 gas, crystallizing on the cooler walls of the tube.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 153,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I, SnI2\",\n        \"synthesis_product\": \"Black MASnI3 Powder\",\n        \"synthesis_description\": \"Place equimolar amounts of SnI2 and MAI in an agate mortar and ground carefully with a pestle until a visually homogeneous, black powder is obtained.\",\n        \"experimental_method\": \"Optical-diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 154,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I, PbI2\",\n        \"synthesis_product\": \"Black MAPbI3 Powder\",\n        \"synthesis_description\": \"Place equimolar amounts of PbI2 and MAI in an agate mortar and ground carefully with a pestle until a visually homogeneous, black powder is obtained.\",\n        \"experimental_method\": \"Optical diffuse reflectance\",\n        \"experimental_description\": \"Measurements were performed at room temperature using a Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm. BaSO4 was used as a nonabsorbing reflectance reference. The generated reflectance-versus-wavelength data were used to estimate the band gap of the material by converting reflectance to absorbance data according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Refer to Page 9029 Figure 9.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 155,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 Polycrystals\",\n        \"synthesis_description\": \"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 \\u00b0C to 46 \\u00b0C over 6 hours and dry (100 \\u00b0C/10 hours). Maintain solution temperature above 40 \\u00b0C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 \\u00b0C.\",\n        \"experimental_method\": \"Diffuse-reflectance UV-Vis absorption\",\n        \"experimental_description\": \"Absorption optical gap is 1.51 eV using diffuse reflectance UV-Vis spectra calculated using the optical absorption coefficient (\\\\alpha) according to the Kubelka-Munk equation. Refer to Page 5637 Figure 11.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"Estimate of optical gap at r.t.p.\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505002\",\n        \"dataset_ID\": 158,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Single Crystal Formamidinium Lead Iodide (FAPbI3): Insight into the Structural, Optical, and Electrical Properties\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2253\",\n        \"pages_end\": \"2258\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead iodide (PbI2 , 99.999%) were purchased from Sigma-Aldrich, formamidinium iodide (FAI) was purchased from Dyesol Limited (Australia), dimethylformamide, ITO\",\n        \"synthesis_product\": \"FAPbI3 Thin film on ITO\",\n        \"synthesis_description\": \"Dissolve 450 mg of PbI2 in 1 mL dimethylformamide and spincoat on indium-tin-oxide (ITO) substrates at 2500 rpm for 30 s. Spincoat FAI (dissolved in 2-propanol) on top of dried PbI2 at room temperature at 3000 rpm for 30 s in dry air. Anneal films in air at 150 \\u00b0C for desired time.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"[ASSUMED] Horiba Jobin Yvon system. Refer to SI Figure S3.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"Photoluminescence peak at 300K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja809598r\",\n        \"dataset_ID\": 159,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organometal Halide Perovskites as Visible-Light Sensitizers for Photovoltaic Cells\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"131\",\n        \"pages_start\": \"6050\",\n        \"pages_end\": \"6051\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"FTO (10 \\u03a9/sq, Nippon Sheet Glass), TiCl4, HI, CH3NH2, PbI2\",\n        \"synthesis_product\": \"MAPbI3 on TiO2-coated FTO, TiO2 film had a thickness of 8-12 \\u03bcm. Powder is black.\",\n        \"synthesis_description\": \"Soak FTO in a 40 mM TiCl4 aqueous solution at 70 \\u00b0C for 30 min to form a thin TiO2 buffer layer. \\r\\n\\r\\nCoat FTO with a commercial nanocrystalline TiO2 paste (refer to SI for more information) using a screen printer and sintering at 480 \\u00b0C for 1 h in air. \\r\\n\\r\\nSynthesize CH3NH3I by reacting HI with 40% methylamine in methanol solution followed by recrystallization.\\r\\n\\r\\nDrop the TiO2 film into an 8 wt % stoichiometric solution of CH3NH3I and PbI2 in \\u03b3-butyrolactone. Subsequent film formation was done by spin-coating.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"X-ray diffraction analysis (Rigaku RINT- 2500). Refer to Page 6050: Paragraph 2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"Lattice parameters at 300K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja809598r\",\n        \"dataset_ID\": 160,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organometal Halide Perovskites as Visible-Light Sensitizers for Photovoltaic Cells\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"131\",\n        \"pages_start\": \"6050\",\n        \"pages_end\": \"6051\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"FTO (10 \\u03a9/sq, Nippon Sheet Glass), TiCl4, HBr, CH3NH2, PbBr2\",\n        \"synthesis_product\": \"MAPbBr3 on TiO2-coated FTO, MAPbBr3 size 2-3mm. TiO2 film had a thickness of 8-12 \\u03bcm. Powder is yellow\",\n        \"synthesis_description\": \"Soak FTO in a 40 mM TiCl4 aqueous solution at 70 \\u00b0C for 30 min to form a thin TiO2 buffer layer. \\r\\n\\r\\nCoat FTO with a commercial nanocrystalline TiO2 paste (refer to SI for more information) using a screen printer and sintering at 480 \\u00b0C for 1 h in air.\\r\\n\\r\\nSynthesize CH3NH3Br by reacting HBr with 40% methylamine in methanol solution followed by recrystallization.\\r\\n\\r\\nDrop the TiO2 film into a 20 wt % stoichiometric solution of CH3NH3Br and PbBr2 in N,N-dimethylformamide. Subsequent film formation was done by spin-coating.\\r\\n\\r\\nThe liquid precursor film coated on the TiO2 gradually changed color simultaneously with drying, indicating the formation of CH3NH3PbBr3 in the solid state.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"X-ray diffraction analysis (Rigaku RINT- 2500). Refer to Page 6050: Paragraph 2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters at 300K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1006/jssc.1995.1023\",\n        \"dataset_ID\": 161,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Transport, Optical, and Magnetic Properties of the Conducting Halide Perovskite CH3NH3SnI3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"114\",\n        \"pages_start\": \"159\",\n        \"pages_end\": \"163\",\n        \"year\": \"1995\",\n        \"synthesis_starting_materials\": \"Tin (II) oxide, HI (aq), ethylene glycol, argon, nitrogen\",\n        \"synthesis_product\": \"Black-green powder.\",\n        \"synthesis_description\": \"Dissolve Tin (II) oxide (10.40 g, 27.9 mmole) in 20 ml of a concentrate (57% by weight) HI (aq) in a test tube under flowing argon. \\r\\n\\r\\nAdd another 8.0 ml of aqueous HI to a test tube containing CH3NH3-HI (4.44g, 27.9 mmole). \\r\\n\\r\\nGently heat solution to 90.0 \\u00b0C in a water/ethylene glycol bath to facilitate dissolution. Mix warm CH3NH2-HI and SNI2 solutions and cool the resulting yellow solution to room temperature.\\r\\n\\r\\nFilter the black-green precipitate that forms under flowing nitrogen and dry under flowing argon at 100 \\u00b0C for 5 hr. Yield is typically 76 %. CH3NH3SnI3 is air sensitive and decomposes in air within several hours. All samples are stored and manipulated for the various measurements in an argon-filled glove box with oxygen and water levels below 1 ppm.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Not specified. Refer to Page 160 Experimental paragraph 1.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1006/jssc.1995.1023\",\n        \"dataset_ID\": 162,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Transport, Optical, and Magnetic Properties of the Conducting Halide Perovskite CH3NH3SnI3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"114\",\n        \"pages_start\": \"159\",\n        \"pages_end\": \"163\",\n        \"year\": \"1995\",\n        \"synthesis_starting_materials\": \"Tin (II) oxide, HI (aq), ethylene glycol, argon, nitrogen\",\n        \"synthesis_product\": \"Black single crystal\",\n        \"synthesis_description\": \"Dissolve Tin (II) oxide (10.40 g, 27.9 mmole) in 20 ml of a concentrate (57% by weight) HI (aq) in a test tube under flowing argon. \\r\\n\\r\\nAdd another 8.0 ml of aqueous HI to a test tube containing CH3NH3-HI (4.44g, 27.9 mmole). \\r\\n\\r\\nGently heat solution to 90.0 \\u00b0C in a water/ethylene glycol bath to facilitate dissolution. Mix warm CH3NH2-HI and SNI2 solutions and cool the resulting yellow solution to room temperature.\\r\\n\\r\\nFilter the black-green precipitate that forms under flowing nitrogen and dry under flowing argon at 100 \\u00b0C for 5 hr. Yield is typically 76 %. CH3NH3SnI3 is air sensitive and decomposes in air within several hours. All samples are stored and manipulated for the various measurements in an argon-filled glove box with oxygen and water levels below 1 ppm.\\r\\n\\r\\nUse 2.0 g of CH3NH3SnI3 and equilibrate at 90.0 \\u00b0C in a water/ethylene glycol bath. Add sufficient HI under flowing argon to dissolve the entire charge (about 11 ml). Cool the solution to -10.0 \\u00b0C at 2 \\u00b0C/hr. The small black crystals grow in a rhombic dodecahedral habit.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Not specified. Refer to Page 160 Experimental paragraph 1,3.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1006/jssc.1997.7593\",\n        \"dataset_ID\": 163,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Resistivity, and Thermal Properties of the Cubic Perovskite NH2CH=NH2SnI3 and Related Systems\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"134\",\n        \"pages_start\": \"376\",\n        \"pages_end\": \"381\",\n        \"year\": \"1997\",\n        \"synthesis_starting_materials\": \"Tin (II) iodide, methylammonium iodide, HI (aq), argon, nitrogen\",\n        \"synthesis_product\": \"Powder\",\n        \"synthesis_description\": \"Dissolve tin(II) iodide (2.235 g, 6 mmol) in flowing argon at 70\\u00b0C in 4 ml of a concentrated (57% by weight) aqueous HI solution. \\r\\n\\r\\nDissolve methylammonium iodide (6 mmol) at room temperature in 1.0 ml of concentrated aqueous hydriodic acid and immediately add to the tin(II) iodide solution (after allowing it to cool). \\r\\n\\r\\nRinse the methylammonium tube using two additional 0.5-ml portions of hydriodic acid and add to the test tube containing the product, which at all times was kept in an inert atmosphere of flowing argon.\\r\\n\\r\\nMaintain the product in the hydriodic acid solution for 15 min at room temperature, with periodic agitation of the solution, and filter under flowing dry nitrogen gas.\\r\\n\\r\\nDry powder under vacuum at room temperature and store in an argon-filled glovebox, with oxygen and water levels maintained below 1 ppm.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Siemens D5000 CuK\\u03b1 radiation, refined using Siemens WIN-METRIC program. Refer to Page 377 X-ray diffraction section.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1006/jssc.1997.7593\",\n        \"dataset_ID\": 164,\n        \"id\": 44,\n        \"compound_name\": \"Formamidinium tin iodide\",\n        \"formula\": \"CH5N2SnI3\",\n        \"group\": \"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"Imidoformamidinium tin (II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Resistivity, and Thermal Properties of the Cubic Perovskite NH2CH=NH2SnI3 and Related Systems\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"134\",\n        \"pages_start\": \"376\",\n        \"pages_end\": \"381\",\n        \"year\": \"1997\",\n        \"synthesis_starting_materials\": \"Tin (II) iodide, formamidine acetate, HI (aq), argon, nitrogen\",\n        \"synthesis_product\": \"Black powder\",\n        \"synthesis_description\": \"Dissolve tin(II) iodide (2.235 g, 6 mmol) in flowing argon at 70\\u00b0C in 4 ml of a concentrated (57% by weight) aqueous HI solution. \\r\\n\\r\\nDissolve formamidine acetate (0.6246 g, 6 mmol) at room temperature in 1.0 ml of concentrated aqueous hydriodic acid and immediately add to the tin(II) iodide solution (after allowing it to cool), leading to a thick black precipitate. \\r\\n\\r\\nRinse the formamidinium tube using two additional 0.5-ml portions of hydriodic acid and add to the test tube containing the product, which at all times was kept in an inert atmosphere of flowing argon.\\r\\n\\r\\nMaintain the product in the hydriodic acid solution for 15 min at room temperature, with periodic agitation of the solution, and filter under flowing dry nitrogen gas.\\r\\n\\r\\nYield was approximately 75% of the theoretical yield. Dry black powder under vacuum at room temperature and store in an argon-filled glovebox, with oxygen and water levels maintained below 1 ppm.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Siemens D5000 CuKalpha radiation, refined using Siemens WIN-METRIC program. Refer to Page 377 X-ray diffraction section.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters at 300K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1006/jssc.1997.7593\",\n        \"dataset_ID\": 165,\n        \"id\": 44,\n        \"compound_name\": \"Formamidinium tin iodide\",\n        \"formula\": \"CH5N2SnI3\",\n        \"group\": \"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"Imidoformamidinium tin (II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Resistivity, and Thermal Properties of the Cubic Perovskite NH2CH=NH2SnI3 and Related Systems\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"134\",\n        \"pages_start\": \"376\",\n        \"pages_end\": \"381\",\n        \"year\": \"1997\",\n        \"synthesis_starting_materials\": \"Tin (II) iodide, formamidine acetate, HI (aq), argon, nitrogen\",\n        \"synthesis_product\": \"Black single crystal\",\n        \"synthesis_description\": \"Dissolve tin(II) iodide (2.235 g, 6 mmol) in flowing argon at 70\\u00b0C in 4 ml of a concentrated (57% by weight) aqueous HI solution. \\r\\n\\r\\nDissolve formamidine acetate (0.6246 g, 6 mmol) at room temperature in 1.0 ml of concentrated aqueous hydriodic acid and immediately add to the tin(II) iodide solution (after allowing it to cool), leading to a thick black precipitate. \\r\\n\\r\\nRinse the formamidinium tube using two additional 0.5-ml portions of hydriodic acid and add to the test tube containing the product, which at all times was kept in an inert atmosphere of flowing argon.\\r\\n\\r\\nMaintain the product in the hydriodic acid solution for 15 min at room temperature, with periodic agitation of the solution, and filter under flowing dry nitrogen gas.\\r\\n\\r\\nYield was approximately 75% of the theoretical yield. Dry black powder under vacuum at room temperature and store in an argon-filled glovebox, with oxygen and water levels maintained below 1 ppm.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius CAD4 diffractometer with graphite-monochromatized MoKalpha (0.7107 angstrom) radiation. Refer to Page 377 X-ray diffraction section.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters at 300K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 166,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",\n        \"synthesis_product\": \"Colorless MAPbCl3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the colorless crystals.\",\n        \"experimental_method\": \"Temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"Not specified.\",\n        \"physical_property\": \">178.8\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters >178.8\",\n        \"space_group\": \"Pm3m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 167,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",\n        \"synthesis_product\": \"Colorless MAPbCl3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the colorless crystals.\",\n        \"experimental_method\": \"Temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"Not specified.\",\n        \"physical_property\": \">172.9\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"Lattice parameters 172.9-178.8\",\n        \"space_group\": \"P4/mmm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 168,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",\n        \"synthesis_product\": \"Colorless MAPbCl3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the colorless crystals.\",\n        \"experimental_method\": \"Temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"Not specified.\",\n        \"physical_property\": \"<172.9\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Lattice parameters <172.9\",\n        \"space_group\": \"P222(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 169,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HBr, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"MAPbBr3 single crystal ~0.1mm, bright red/orange\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbBr3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 48 wt% HBr aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add another 2 ml of HBr solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days. Refer to Page 9299 Section 2.1 Synthesis; Figure 1.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Bruker D8 Advance diffractometer (Bragg\\u2013Brentano geometry) equipped with a Cu-Ka X-ray tube operated at 40 kV and 40 mA. Refer to Page 9300 Section 3.1 Paragraph 2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters at 300K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 170,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HCl, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Colorless MAPbCl3 Single crystal ~1mm\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbCl3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated aquous HCl solution (37 wt%) warmed (~90 \\u00b0C) in a water bath. Then add an excess of HCl to prevent the co-precipitation of PbCl2 in agreement with previous work [2], along with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Bruker D8 Advance diffractometer (Bragg\\u2013Brentano geometry) equipped with a Cu-Ka X-ray tube operated at 40 kV and 40 mA. Refer to Page 9300 Section 3.1 Paragraph 2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters at 298K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 171,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HBr, CH3NH2, Pb(NO3)2\",\n        \"synthesis_product\": \"MAPbBr3 Single-crystal\",\n        \"synthesis_description\": \"Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100\\u00b0C to the concentrated CH3NH3Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Yield: 9.5 g.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"CAD-4 four-circle diffractometer; Mo K\\u03b1, \\u03bb = 0.70926 \\u00c5 (graphite monochromator); T = 18 \\u00b0C. Lorentz, polarization, and absorption corrections applied. Refer to page 413 Experimental.\",\n        \"physical_property\": \"291.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters at 300K\",\n        \"space_group\": \"Pm3m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 172,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HCl, CH3NH2, PbCl2\",\n        \"synthesis_product\": \"MAPbCl3 Single-crystal\",\n        \"synthesis_description\": \"Primarily referenced the methods of [1] and [2]. The synthesis of MAPbBr3 in ref [2] was modified to prepare MAPbCl3.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"CAD-4 four-circle diffractometer; Mo K\\u03b1, \\u03bb = 0.70926 \\u00c5 (graphite monochromator); T = 18 \\u00b0C. Lorentz, polarization, and absorption corrections applied. Refer to page 413 Experimental.\",\n        \"physical_property\": \"291.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Lattice parameters at 291K\",\n        \"space_group\": \"Pm3m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 173,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HI, CH3NH2, Pb(NO3)2\",\n        \"synthesis_product\": \"MAPbI3 Powder\",\n        \"synthesis_description\": \"Add concentrated HI to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100\\u00b0C to the concentrated CH3NH2I solution. Organic crystals form while dripping in the solution. Cool the solution to not below 40\\u00b0C and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Diffraction pattern of some of the lines corresponding to Weber's cubic (a = 6.27 A) were split up or broadened, indicating that MAPbI3 at room temperature is not strictly cubic. Refer to page 413 Experimental.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"Lattice parameters at 300K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1143/JPSJ.71.1694\",\n        \"dataset_ID\": 174,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Study on Cubic\\u2013Tetragonal Transition of CH3NH3PbI3\",\n        \"journal\": \"Journal of the Physical Society of Japan\",\n        \"vol\": \"71\",\n        \"pages_start\": \"1694\",\n        \"pages_end\": \"1697\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"CH3NH3PbI3, lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",\n        \"synthesis_product\": \"Black and opaque MAPbI3 Single crystal\",\n        \"synthesis_description\": \"CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ (by adding a 40% solution of CH3NH2 in water) dissolved in concentrated HI solution. Cool aqueous solution from l00\\u00b0C to not lower than 40\\u00b0C to obtain a black crystal. Crystals of about 1 cm in dimension were obtained. Synthesis using reference [2].\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Spherical samples were cut and polished into 0.3mm in diameter, among which a single crystal was selected and was mounted on an off-centered 4-circle diffractometer (HUBER 424) controlled by MXC (Mac Science). Graphite-monochromated Mo K\\\\alpha radiation was used from a rotating anode generator with 50 kV\\u2013250 mA. Refer to Page 1695 Table I (Params); Page 1696 Table II (Apos).\",\n        \"physical_property\": \"220.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 176,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black MASnI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, elongated, rhombic dodecahedral (12 faces) crystals of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 1.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"P4mm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 178,\n        \"id\": 44,\n        \"compound_name\": \"Formamidinium tin iodide\",\n        \"formula\": \"CH5N2SnI3\",\n        \"group\": \"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"Imidoformamidinium tin (II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HC(NH2)2I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black FASnI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black rhombic dodecahedral crystals (12 faces) of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 1.\",\n        \"physical_property\": \"340.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Amm2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 179,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I [from syn], PbI2 [from syn], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave solution to cool back to room temperature. Upon cooling, black, rhombic dodecahedral crystals (12 faces) of the title compound precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 1.\",\n        \"physical_property\": \"400.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"P4mm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 182,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HC(NH2)2I, PbI2,distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black FAPbI3 Crystals (alpha phase)\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Stop stirring and leave the solution to evaporate at 100 \\u00b0C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. After standing for 2-3 h at 100 \\u00b0C, under a nitrogen atmosphere, set the temperature to 80 \\u00b0C for a further 2-3 h. Repeat the previous step for two more times to reach 60 \\u00b0C and 40 \\u00b0C at which point the solution was left to come to room temperature by powering off the hotplate. The crystals were collected by filtration and washed with anhydrous EtOH.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to page 9025 Table 1.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"P3m1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 183,\n        \"id\": 42,\n        \"compound_name\": \"Methylammonium tin iodide\",\n        \"formula\": \"CH3NH3SnI3\",\n        \"group\": \"methanaminium triiodostannate(II), MASI, (MA)SnI3, (CH3NH3)SnI3\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"methanammonium tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate the solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black, elongated, rhombic dodecahedral (12 faces) crystals of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\",\n        \"physical_property\": \"200.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"I4cm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 184,\n        \"id\": 44,\n        \"compound_name\": \"Formamidinium tin iodide\",\n        \"formula\": \"CH5N2SnI3\",\n        \"group\": \"Methanimidamide triiodostannate(II), FASI, FASnI3, HC(NH2)2SnI3, (NH2)2CHSnI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"Imidoformamidinium tin (II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HC(NH2)2I [from synthesis], SnI2 [from synthesis], distilled HI (57% aqueous) (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black FASnI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve SnI2 (372 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate the solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave the solution to cool back to room temperature. Upon cooling, black rhombic dodecahedral crystals (12 faces) of the title compound were precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\",\n        \"physical_property\": \"180.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imm2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 185,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"CH3NH3I [from syn], PbI2 [from syn], distilled HI 57% (99.95%), H3PO2 50%\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid CH3NH3I (159 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Discontinue stirring and leave solution to cool back to room temperature. Upon cooling, black, rhombic dodecahedral crystals (12 faces) of the title compound precipitated. Leave crystals to grow for a further 24 h under a nitrogen atmosphere before filtering and washing copiously with degassed EtOH. Yield 70-90%.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either an STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"I4cm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 186,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 Polycrystals\",\n        \"synthesis_description\": \"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 \\u00b0C to 46 \\u00b0C over 6 hours and dry (100 \\u00b0C/10 hours). Maintain solution temperature above 40 \\u00b0C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 \\u00b0C.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Tetragonal/cubic phase transition was investigated using variable temperature powder X-ray diffraction. In situ XRD data were collected in asymmetric reflection mode under a static helium atmosphere on an INEL Equinox 3000 (Inel, Artenay, France) equipped with an XRK-900 reactor chamber (Anton-Paar, Graz, Austria), a curved position sensitive detector (Ine, Artenay, France), a copper Ka source and a Ge-(111) focusing mirror. Refer to Page 5636 Table 4.\",\n        \"physical_property\": \"25.0\",\n        \"unit\": \"\\u00b0C\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C5CP02605A\",\n        \"dataset_ID\": 187,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Characterization of an abnormal photoluminescence behavior upon crystal-phase transition of perovskite CH3NH3PbI3\",\n        \"journal\": \"Physical Chemistry Chemical Physics\",\n        \"vol\": \"17\",\n        \"pages_start\": \"16405\",\n        \"pages_end\": \"16411\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 \\u00b0C for 2 h. Evaporate solvents at 50 \\u00b0C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 \\u00b0C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2: NH4OH: H2O = 1: 1: 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 \\u00b0C.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"The MAPbI3 film was characterized by X-ray diffraction (XRD) on a PANalytical X-ray diffractometer (Model EMPYREAN) with a monochromatic Cu Ka1 radiation. The lattice parameters were precisely determined using Si powders as the internal standard reference material. Refer to ESI Table SI.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C5CP02605A\",\n        \"dataset_ID\": 188,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Characterization of an abnormal photoluminescence behavior upon crystal-phase transition of perovskite CH3NH3PbI3\",\n        \"journal\": \"Physical Chemistry Chemical Physics\",\n        \"vol\": \"17\",\n        \"pages_start\": \"16405\",\n        \"pages_end\": \"16411\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 \\u00b0C for 2 h. Evaporate solvents at 50 \\u00b0C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 \\u00b0C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 \\u00b0C.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"The MAPbI3 film was characterized by X-ray diffraction (XRD) on a PANalytical X-ray diffractometer (Model EMPYREAN) with a monochromatic Cu Ka1 radiation. The lattice parameters were precisely determined using Si powders as the internal standard reference material. Refer to ESI Table SI.\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 189,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 polycrystals\",\n        \"synthesis_description\": \"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 \\u00b0C to 46 \\u00b0C over 6 hours and dry (100 \\u00b0C/10 hours). Maintain solution temperature above 40 \\u00b0C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 \\u00b0C.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Tetragonal/cubic phase transition was investigated using variable temperature powder X-ray diffraction. In situ XRD data were collected in asymmetric reflection mode under a static helium atmosphere on an INEL Equinox 3000 (Inel, Artenay, France) equipped with an XRK-900 reactor chamber (Anton-Paar, Graz, Austria), a curved position sensitive detector (Ine, Artenay, France), a copper Ka source and a Ge-(111) focusing mirror. Refer to Page 5636 Table 4.\",\n        \"physical_property\": \"333.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 190,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 \\u00b0C for 2 h with constant stirring. Evaporate at 50 \\u00b0C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 \\u00b0C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 \\u00b0C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 \\u00b0C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution-grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5\\u00b0 2theta. Refer to Page 5637 Table 8.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 191,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 \\u00b0C for 2 h with constant stirring. Evaporate at 50 \\u00b0C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 \\u00b0C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 \\u00b0C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 \\u00b0C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5\\u00b0 2theta. Refer to Page 5637 Table 8.\",\n        \"physical_property\": \"152.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c4cc09944c\",\n        \"dataset_ID\": 192,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Complete structure and cation orientation in the perovskite photovoltaic methylammonium lead iodide between 100 and 352 K\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"51\",\n        \"pages_start\": \"4180\",\n        \"pages_end\": \"4183\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead acetate, HI (aq., 57 wt%), CH3NH2 (aq., 40%)\",\n        \"synthesis_product\": \"Yellow MAPbI3 thin film (10 nm grain size)\",\n        \"synthesis_description\": \"Dissolve 2.5 g of lead acetate (Sigma) in 10 mL hydroiodic acid (aq., 57 wt%, Sigma) in a 50 mL round bottom flask and heat to 100 \\u00b0C in an oil bath. \\r\\n\\r\\nAdd 0.597 g of CH3NH2 (aq., 40%, Sigma) dropwise to a further 2 mL of hydroiodic acid kept at 0 \\u00b0C in an ice bath under stirring. \\r\\n\\r\\nAdd the methylammonium iodide solution to the lead acetate solution and cool over two hours to 46 \\u00b0C, affording a black precipitate.\\r\\n\\r\\nFilter and dry the black precipitate for 12 h at 100 \\u00b0C. Average yield was 3.1 g, 75.2%. Repeat until 8 g of product has been obtained.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"Data were collected using the D20 instrument at the ILL Grenoble operating in high take-off angle, higher resolution mode. 8 g of finely ground MAPbI3 was placed in a 7 mm diameter vanadium can. Data were collected for 90 minutes at 100 K. Raw diffraction data were corrected against detector efficiency and analysed using the GSAS/EXPGUI program suite; structure refinements for the long data collections at 100, 180 and 350 K were undertaken as described in the ESI. Refer to a,b,c, space group from ESI Table S1.1, volume from Garnett PRL, Structure Refinement from ESI.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c4cc09944c\",\n        \"dataset_ID\": 193,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Complete structure and cation orientation in the perovskite photovoltaic methylammonium lead iodide between 100 and 352 K\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"51\",\n        \"pages_start\": \"4180\",\n        \"pages_end\": \"4183\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead acetate, HI (aq., 57 wt%), CH3NH2 (aq., 40%)\",\n        \"synthesis_product\": \"Yellow MAPbI3 thin film (10 nm grain size)\",\n        \"synthesis_description\": \"Dissolve 2.5 g of lead acetate (Sigma) in 10 mL hydroiodic acid (aq., 57 wt%, Sigma) in a 50 mL round bottom flask and heat to 100 \\u00b0C in an oil bath. \\r\\n\\r\\nAdd 0.597 g of CH3NH2 (aq., 40%, Sigma) dropwise to a further 2 mL of hydroiodic acid kept at 0 \\u00b0C in an ice bath under stirring. \\r\\n\\r\\nAdd the methylammonium iodide solution to the lead acetate solution and cool over two hours to 46 \\u00b0C, affording a black precipitate.\\r\\n\\r\\nFilter and dry the black precipitate for 12 h at 100 \\u00b0C. Average yield was 3.1 g, 75.2%. Repeat until 8 g of product has been obtained.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"Data were collected using the D20 instrument at the ILL Grenoble operating in high take-off angle, higher resolution mode. 8 g of finely ground MAPbI3 was placed in a 7 mm diameter vanadium can. Data were collected for 90 minutes at 352 K. Raw diffraction data were corrected against detector efficiency and analysed using the GSAS/EXPGUI program suite; structure refinements for the long data collections at 100, 180 and 350 K were undertaken as described in the ESI. Refer to ESI Table S3.1.\",\n        \"physical_property\": \"352.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 194,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-GGA\",\n        \"k_point_grid\": \"7x5x7\",\n        \"level_of_relativity\": \"Non-relativistic\",\n        \"basis_set_definition\": \"Plane-wave with cutoff 900 eV\",\n        \"numerical_accuracy\": \"Tolerance for energy minimization 10e-9 eV/atom.\\r\\ninteratomic forces after relaxation were below 0.005 eV/\\u00c5, and the stresses were below 0.05 GPa\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 195,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-GGA\",\n        \"k_point_grid\": \"2x5x7\",\n        \"level_of_relativity\": \"Non-relativistic\",\n        \"basis_set_definition\": \"Plane-wave with cutoff 900 eV\",\n        \"numerical_accuracy\": \"Tolerance: 10e-9 eV\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 197,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",\n        \"synthesis_product\": \"Black d6-MAPbI3 powder\",\n        \"synthesis_description\": \"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \\r\\n\\r\\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \\r\\n\\r\\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 \\u00b0C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",\n        \"experimental_method\": \"Neutron diffraction\",\n        \"experimental_description\": \"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The sample size was ~5.5 g for the d6-MAPbI. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to SI: Supplementary Table 1 and Additional dataset; CCDC.\",\n        \"physical_property\": \"10.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 198,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",\n        \"synthesis_product\": \"Black d6-MAPbI3 powder\",\n        \"synthesis_description\": \"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI.\\r\\n\\r\\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box.\\r\\n\\r\\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 \\u00b0C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",\n        \"experimental_method\": \"Neutron diffraction\",\n        \"experimental_description\": \"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The sample size was ~5.5 g for the d6-MAPbI. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to SI: Supplementary Table 4 and Additional dataset; CCDC.\",\n        \"physical_property\": \"190.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"I 4/m c m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 199,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",\n        \"synthesis_product\": \"Black d6-MAPbI3 powder\",\n        \"synthesis_description\": \"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \\r\\n\\r\\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \\r\\n\\r\\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 \\u00b0C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",\n        \"experimental_method\": \"Neutron diffraction\",\n        \"experimental_description\": \"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The sample size was ~5.5 g for the d6-MAPbI. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to SI: Supplementary Table 5.\",\n        \"physical_property\": \"350.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"P m 3 m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 200,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CD3NH2 (Sigma-Aldrich, 99 atom % D)\",\n        \"synthesis_product\": \"CD3NH3PbI3\",\n        \"synthesis_description\": \"The CD3NH3PbI3 was prepared using CD3NH2 that was 99 atom % D. \\r\\n\\r\\nSynthesis perovskite using a similar method as 4-a.\",\n        \"experimental_method\": \"Neutron diffraction\",\n        \"experimental_description\": \"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to Additional dataset; CCDC.\",\n        \"physical_property\": \"10.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P m 3 m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 201,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CH3NH2, HI, D2O\",\n        \"synthesis_product\": \"CH3ND3PbI3\",\n        \"synthesis_description\": \"Preparation of CH3ND3I:\\r\\nReact methylamine gas with HI to yield methyl ammonium iodide. Exchange the two H atoms attached to the nitrogen atoms with D by dissolving the salt in 10 ml D2O (99 atom % D), drying under vacuum, and then repeating two more times. The resulting CH3ND3I was estimated to be better than 98 atom% D on the ammonium group. \\r\\n\\r\\nSynthesis perovskite using a similar method as 4-a.\",\n        \"experimental_method\": \"Neutron diffraction\",\n        \"experimental_description\": \"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Refer to Additional dataset; CCDC.\",\n        \"physical_property\": \"10.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P n m a\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"doi:10.1016/S0022-4596(03)00352-9\",\n        \"dataset_ID\": 202,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase transitions in the perovskite methylammonium lead bromide, CH3ND3PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"176\",\n        \"pages_start\": \"97\",\n        \"pages_end\": \"104\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"CH3ND3PbBr3 powder\",\n        \"synthesis_description\": \"Samples were prepared following well-described methods [1,2]. \\r\\n\\r\\nIn the case of the neutron sample, N-deuterated MAPB was produced by using fully deuterated DBr (MSD Isotopes), and reactor grade (499.8%) D2O (Atomic Energy of Canada Limited\\u2014AECL). The D2O was also used to deuterate all exchangeable hydrogens of the precursor chemicals prior to the final synthesis. A fine bright orange precipitate was formed which was filtered and transferred to a desiccating chamber prior to the diffraction measurements.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"C2 diffractometer at Chalk River Laboratories, Chalk River, Ontario. The incident wavelength for Rietveld refinements: 1.32860(3)A\\u02da. Data were collected and refined in two separate banks from 3\\u201383\\u00b0 and 37\\u2013117\\u00b0 theta with wire-spacing 0.1\\u00b0 over the temperature range of 11\\u2013250K. Each bank was collected for 1 h. Refer to Page 104 Table 4.\",\n        \"physical_property\": \"11.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"doi:10.1016/S0022-4596(03)00352-9\",\n        \"dataset_ID\": 203,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase transitions in the perovskite methylammonium lead bromide, CH3ND3PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"176\",\n        \"pages_start\": \"97\",\n        \"pages_end\": \"104\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"CH3ND3PbBr3 powder\",\n        \"synthesis_description\": \"Samples were prepared following well-described methods [1,2]. \\r\\n\\r\\nIn the case of the neutron sample, N-deuterated MAPB was produced by using fully deuterated DBr (MSD Isotopes), and reactor grade (499.8%) D2O (Atomic Energy of Canada Limited\\u2014AECL). The D2O was also used to deuterate all exchangeable hydrogens of the precursor chemicals prior to the final synthesis. A fine bright orange precipitate was formed which was filtered and transferred to a desiccating chamber prior to the diffraction measurements.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"C2 diffractometer at Chalk River Laboratories, Chalk River, Ontario. The incident wavelength for Rietveld refinements: 1.32860(3)A\\u02da. Data were collected and refined in two separate banks from 3\\u201383 \\u00b0 and 37\\u2013117 \\u00b0 2theta with wire-spacing 0.1 \\u00b0 over the temperature range of 11\\u2013250K. Each bank was collected for 1 h. Refer to Page 104 Table 4.\",\n        \"physical_property\": \"160.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"doi:10.1016/S0022-4596(03)00352-9\",\n        \"dataset_ID\": 204,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase transitions in the perovskite methylammonium lead bromide, CH3ND3PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"176\",\n        \"pages_start\": \"97\",\n        \"pages_end\": \"104\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"CH3ND3PbBr3 powder\",\n        \"synthesis_description\": \"Samples were prepared following well-described methods [1,2]. \\r\\n\\r\\nIn the case of the neutron sample, N-deuterated MAPB was produced by using fully deuterated DBr (MSD Isotopes), and reactor grade (499.8%) D2O (Atomic Energy of Canada Limited\\u2014AECL). The D2O was also used to deuterate all exchangeable hydrogens of the precursor chemicals prior to the final synthesis. A fine bright orange precipitate was formed which was filtered and transferred to a desiccating chamber prior to the diffraction measurements.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"C2 diffractometer at Chalk River Laboratories, Chalk River, Ontario. Incident wavelength for Rietveld refinements: 1.32860(3)A\\u02da. Data were collected and refined in two separate banks from 3\\u201383 \\u00b0 and 37\\u2013117 \\u00b0 2theta with wire-spacing 0.1 \\u00b0 over the temperature range of 11\\u2013250K. Each bank was collected for 1 h. Refer to Page 104 Table 4.\",\n        \"physical_property\": \"225.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 205,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HC(NH2)2I, PbI2, distilled HI 57% aqueous (99.95%), H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"Black FAPbI3 Crystals (alpha phase)\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Stop stirring and leave solution to evaporate at 100 \\u00b0C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. After standing for 2-3 h at 100 \\u00b0C, under a nitrogen atmosphere, set temperature to 80 \\u00b0C for a further 2-3 h. Repeat the previous step for two more times to reach 60 \\u00b0C and 40 \\u00b0C at which point the solution was left to come to room temperature by powering off the hotplate. The crystals were collected by filtration and washed with anhydrous EtOH.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 2.\",\n        \"physical_property\": \"150.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"P3\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic401215x\",\n        \"dataset_ID\": 206,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Tin and Lead Iodide Perovskites with Organic Cations: Phase Transitions, High Mobilities, and Near-Infrared Photoluminescent Properties\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"52\",\n        \"pages_start\": \"9019\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HC(NH2)2I, PbI2, distilled HI 57% (99.95%), H3PO2 50%\",\n        \"synthesis_product\": \"Yellow FAPbI3 Crystals (delta phase)\",\n        \"synthesis_description\": \"Charge 100 ml 2-necked round bottom flask with a mixture of aqueous HI (6.8 ml, 7.58M) and aqueous H3PO2 (1.7 ml, 9.14M). The liquid was degassed by passing a stream of nitrogen through it for 1 min and keeping it under a nitrogen atmosphere throughout the experiment. Dissolve PbI2 (462 mg, 1 mmol) in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. Add solid HC(NH2)2I (172 mg, 1 mmol). Evaporate solution to approximately half its original volume by heating at 120 \\u00b0C. Stop stirring and leave solution to evaporate at 100 \\u00b0C. Black hexagonal (8 faces) or trigonal (5 faces) crystals of the title compound were precipitated and grown at this temperature. Discontinue heating and cool the mixture to room temperature. After 4-5 h the black crystals fully convert to yellow ones of essentially the same shape. Collect yellow crystals by filtration and wash copiously with anhydrous EtOH. Yield 50-60%. The crystals are insensitive on exposure to the atmosphere but spontaneously hydrolyse to yellow PbI2 upon wetting in H2O.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction experiments were performed using either a STOE IPDS II or IPDS 2T diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA. Integration and numerical absorption corrections were performed using the X-AREA, X-RED, and X-SHAPE programs. Refer to Page 9025 Table 3.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P6(3)mc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 207,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 \\u00b0C for 2 h with constant stirring. Evaporate at 50 \\u00b0C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 \\u00b0C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 \\u00b0C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 \\u00b0C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5\\u00b0 2theta. Refined. Refer to Page 5636 Table 6, 7.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 208,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Agilent Supernova diffractometer (Mo K\\u03b1, \\u03bb = 0.71073 \\u00c5) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibrate for at least one hour after the phase transition to obtain a higher quality dataset. Automated data processing and indexing procedures contained within the CrysAlisPro software. Refer to Page 9304 Section 3.4 Paragraph 2.\",\n        \"physical_property\": \"343.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c4cc09944c\",\n        \"dataset_ID\": 212,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Complete structure and cation orientation in the perovskite photovoltaic methylammonium lead iodide between 100 and 352 K\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"51\",\n        \"pages_start\": \"4180\",\n        \"pages_end\": \"4183\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead acetate, HI (aq., 57 wt%), CH3NH2 (aq., 40%)\",\n        \"synthesis_product\": \"Yellow MAPbI3 thin film (10 nm grain size)\",\n        \"synthesis_description\": \"Dissolve 2.5 g of lead acetate (Sigma) in 10 mL hydroiodic acid (aq., 57 wt%, Sigma) in a 50 mL round bottom flask and heat to 100 \\u00b0C in an oil bath. \\r\\n\\r\\nAdd 0.597 g of CH3NH2 (aq., 40%, Sigma) dropwise to a further 2 mL of hydroiodic acid kept at 0 \\u00b0C in an ice bath under stirring. \\r\\n\\r\\nAdd the methylammonium iodide solution to the lead acetate solution and cool over two hours to 46 \\u00b0C, affording a black precipitate.\\r\\n\\r\\nFilter and dry the black precipitate for 12 h at 100 \\u00b0C. Average yield was 3.1 g, 75.2%. Repeat until 8 g of product has been obtained.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"Data were collected using the D20 instrument at the ILL Grenoble operating in high take-off angle, higher resolution mode. 8 g of finely ground MAPbI3 was placed in a 7 mm diameter vanadium can. Data were collected for 90 minutes at 180 K. Raw diffraction data were corrected against detector efficiency and analysed using the GSAS/EXPGUI program suite; structure refinements for the long data collections at 100, 180 and 350 K were undertaken as described in the ESI. Refer to ESI Table S2.1.\",\n        \"physical_property\": \"180.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1006/jssc.1999.8281\",\n        \"dataset_ID\": 216,\n        \"id\": 2,\n        \"compound_name\": \"Bis(phenylethylammonium) lead chloride\",\n        \"formula\": \"C16H24N2PbCl4\",\n        \"group\": \"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PEA)2PbCl4, (C8H12N)2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Layered Solution Crystal Growth Technique and the Crystal Structure of (C6H5C2H4NH3)2PbCl4\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"145\",\n        \"pages_start\": \"694\",\n        \"pages_end\": \"704\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, methanol, phenethylamine\",\n        \"synthesis_product\": \"Small block-like crystals to larger plate-like crystals\",\n        \"synthesis_description\": \"Layered solution approach.\\r\\n\\r\\nGrow crystals within a long, straight, glass tube (Refer to Fig. 1). First dissolve 1.0 mmol (0.278 g) of freshly sublimed PbCl2 (Aldrich; 99.999%) in 7.5 ml concentrated (37 wt %) aqueous HCl (Aldrich; 99.999%). Weigh and add PbCl2 to the tube in an argon-filled glove box, with oxygen and water levels maintained below 1 ppm. Cover the tube with a septum before removing the glove box and adding HCl with a syringe. \\r\\n\\r\\nCreate a second layer in the crystal tube by gently syringing 15 ml of methanol (Aldrich; anhydrous, 99.8%) on top of the HCl/PbCl2 solution. A relatively sharp interface can be created between the solvent layers due to density differences. On top of the column, add a stoichiometric amount (2 mmol or approximately 0.25 ml) of phenethylamine with a syringe. \\r\\n\\r\\nIn the experiment, the phenethylamine rapidly dispersed in the methanol but, because of the sharp interface with the HCl solution, formation of the final (C6H5C2H4NH3)2PbCl4 product was very slow. The crystals were isolated after approximately one year by removing the solvent with a syringe and drying the crystals under vacuum at room temperature and later stored in an argon glove box.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A colorless single crystal of dimensions 0.09 mm X 0.18 mm X 0.27 mm was used. A full sphere of data was collected at room temperature on a Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo K\\u03b1 radiation, \\u03bb = 0.71073 \\u00c5). Refer to page 695 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 217,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"AEQT.2HBr, PbBr2, ethylene glycol, HBr (48% in water)\",\n        \"synthesis_product\": \"Yellow (AEQT)PbBr4 crystals\",\n        \"synthesis_description\": \"Prepare the starting AEQT.2HBr salt using a technique similar to that described in detail for the synthesis of AMQT.2HCl [1]. \\r\\n\\r\\nGrow (AEQT)PbBr4 crystals from a slowly cooled, saturated, aqueous solution containing the organic and inorganic salts. First, weigh 14.5 mg (0.025 mmol) of AEQT.2HBr and 18.3 mg (0.050 mmol) of PbBr2 and add to a test tube under an inert atmosphere. Dissolve the contents in the sealed tube at 120 \\u00b0C in a solvent mixture of 22 mL of deionized water, 1 mL of ethylene glycol, and 2 drops of 48% aqueous HBr, forming a nominally saturated yellow solution. Slow cool at 2 \\u00b0C/h to 0 \\u00b0C, to form small, yellow, sheetlike crystals of the desired (AEQT)PbBr4 compound. To prevent deforming the thin crystals, remove the product from the reaction tube using a pipet and deposit on filter paper to absorb the solution.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"An (AEQT)PbBr4 crystal, with the approximate dimensions 0.01 mm X 0.27 mm X 0.30 mm, was selected under a microscope and attached to the end of a quartz fiber with 5 min epoxy. A full sphere of data was collected at room temperature on a Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo Ka radiation). Refer to Page 6247 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 218,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1515/ncrs-1999-0320\",\n        \"dataset_ID\": 220,\n        \"id\": 4,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead chloride\",\n        \"formula\": \"C30H28N2PbCl4\",\n        \"group\": \"bis(anthracen-1-ylmethanaminium) tetrachloroplumbate(II), AMA2PbCl4, (C15H11NH3)2PbCl4, (C15H14N)2PbCl4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(anthracen-1-ylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"AMA2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal structure of bis(2-anthrylmethylammonium) lead tetrachloride, (C15H11NH3)2PbCl4\",\n        \"journal\": \"Zeitschrift f\\u00fcr Kristallographie - New Crystal Structures\",\n        \"vol\": \"214\",\n        \"pages_start\": \"335\",\n        \"pages_end\": \"336\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"Lead chloride, 2-anthrylmethyl-amine, HCl, DMF\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Prepare 2-anthrylmethyl-amine from the procedure outlined in [1] and [2]. Prepare the adjunct hydrochloride salt by adding a stoichiometric amount of 37% concentrated HCl.\\r\\n\\r\\nSlowly evaporate the solvent from a solution of lead chloride and 2-anthrylmethyl-ammonium chloride with the stoichiometric 1:2 in dimethylformamide.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Nicolet P3, Wyckoff with Mo Ka radiation (0.71073 \\u00c2). Programs used were SHELXS-86 and SHELXL-93.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Fmm2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.2138/am-2002-8-917\",\n        \"dataset_ID\": 221,\n        \"id\": 5,\n        \"compound_name\": \"Calcium titanate\",\n        \"formula\": \"CaTiO3\",\n        \"group\": \"Perovskite, Calcium dioxido(oxo)titanium, Calcium titanate, CaTiO3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"CaTiO3\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure change of Ca1-x SrxTiO3 perovskite with composition and pressure\",\n        \"journal\": \"American Mineralogist\",\n        \"vol\": \"87(8-9)\",\n        \"pages_start\": \"1183\",\n        \"pages_end\": \"1189\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"CaTiO3 powder, TiO2\",\n        \"synthesis_product\": \"crystals with a maximum size of 1000 \\u2022 400 \\u2022 500 mm\",\n        \"synthesis_description\": \"Powder of CaTiO3 was heated with TiO2 flux at 1650 deg C for 24 hours. The temperature was gradually decreased by 5 deg C/hour to 1500 deg C.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A four-circle diffractometer (RIGAKU AFC-5 and AFC-6) using MoKa radiation (l = 0.71069 \\u00c5) emitted from a rotating anode X-ray generator (50 kV, 180 mA) with a graphite monochromator was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbnm\",\n        \"extraction_method\": \"Atomic Simulation Environment (ASE), The American Mineralogist Crystal Structure Database\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 222,\n        \"id\": 6,\n        \"compound_name\": \"Bis(2-(2-naphthyl)ethanammonium) lead iodide\",\n        \"formula\": \"C24H28N2PbI4\",\n        \"group\": \"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(2-naphthyl)ethane-1-aminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"NEA2PbI4, (C24H28N2)PbI4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbI2 (99.999% trace metal basis), HI (57 wt % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), CH3OH (>99.9%), 2-(2-naphthyl)ethanamine (NEA, 95%)\",\n        \"synthesis_product\": \"Red and laminar crystals.\",\n        \"synthesis_description\": \"Dissolve PbI2 (27.0 mg) in 0.5 mL of HI (57%). Place CH3OH (1 ml) on top of the PbI2 solution. Add 0.020 mL of NEA liquid into the CH3OH layer. Crystals would form in the solution overnight.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pn\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 223,\n        \"id\": 7,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead bromide\",\n        \"formula\": \"C22H24N2PbBr4\",\n        \"group\": \"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"NMA2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HBr (48 wt % in H2O, assay >99.99%), 1-(2-Naphthyl)methanamine (95+%) in methanol, PbBr2 (99.999% trace metal basis), DMF\",\n        \"synthesis_product\": \"Colorless and laminar crystals.\",\n        \"synthesis_description\": \"Add a stoichiometric amount of 48% concentrated HBr into the NMA methanol solution to prepare NMA\\u00b7HBr. Evaporate methanol to form colorless NMA\\u00b7HBr crystals. Separate the crystals. Dissolve NMA\\u00b7HBr (9.5 mg) and PbBr2 (7.3 mg) into DMF (0.2 mL). Separate the crystals after the partial evaporation of DMF.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 224,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbBr2 (99.999% trace metal basis), phenylmethylamine (PMA, >99.0%), HBr (48 wt % in H2O, assay >99.99%), CH3OH (>99.9%)\",\n        \"synthesis_product\": \"Colorless and laminar crystals.\",\n        \"synthesis_description\": \"Dissolve PbBr2 (50.3 mg) in 0.5 mL of HBr (48%). Place CH3OH (1 ml) on the top of the PbBr2 solution. Add 0.030 mL of PMA liquid into the CH3OH layer. Expect to form crystals in the solution overnight.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 225,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            745,\n            1901,\n            1903,\n            2267,\n            2269\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbI2 (99.999% trace metal basis), HI (57 wt % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), CH3OH (>99.9%), 2-phenylethylamine (PEA, 99%)\",\n        \"synthesis_product\": \"Red and laminar crystals.\",\n        \"synthesis_description\": \"Dissolve PbI2 (54.6 mg) in 0.5 mL of HI (57%). Place CH3OH (1 ml) on the top of the PbI2 solution. Add 0.030 mL of PEA liquid into the CH3OH layer. Crystals would form in the solution overnight.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 226,\n        \"id\": 10,\n        \"compound_name\": \"Bis(2-(2-naphtyl)ethanammonium) lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbBr2 (99.999% trace metal basis), HBr (48 wt % in H2O, assay >99.99%), CH3OH (>99.9%), 2-(2-naphthyl)ethanamine (NEA, 95%)\",\n        \"synthesis_product\": \"Colorless and laminar crystals.\",\n        \"synthesis_description\": \"Dissolve PbBr2 (21.5 mg) in 0.5 mL of HBr (48%). Place CH3OH (1 ml) on top of the PbBr2 solution. Add 0.020 mL of NEA liquid into the CH3OH layer. Crystals would form in the solution overnight.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using a Bruker D8 ADVANCE Series II at room temperature. The crystal structures were solved and refined by Shelxl and Olex software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1107/S160053680903712X\",\n        \"dataset_ID\": 227,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1890,\n            1900,\n            1902,\n            1905,\n            1906,\n            1907,\n            1908\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Poly[bis(phenethylammonium) [di-bromido-plumbate(II)]-di-\\u03bc-bromido]]\",\n        \"journal\": \"Acta Crystallographica\",\n        \"vol\": \"65\",\n        \"pages_start\": \"m1323\",\n        \"pages_end\": \"m1324\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"Not stated.\",\n        \"synthesis_product\": \"Crystals\",\n        \"synthesis_description\": \"Grown at room temperature from a solution in N,Ndimethylformamide (DMF) using nitromethane as the poor solvent.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Rigaku R-AXIS RAPID diffractometer with Mo K\\u0003a radiation. Refer to the first page of the paper for details.\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1515/znb-1999-1112\",\n        \"dataset_ID\": 228,\n        \"id\": 12,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Preparation and Characterization of [C6H5CH2 NH3]2PbI4, [C6H5CH2CH2SC(NH2)2]3 PbI5 and [C10H7CH2NH3]PbI3 Organic-Inorganic Hybrid Compounds\",\n        \"journal\": \"Z. Naturforsch\",\n        \"vol\": \"54 b\",\n        \"pages_start\": \"1405\",\n        \"pages_end\": \"1409\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"PbI2 (Johnson Matthey, 976204), PbO (Ferak 01-881), hydroiodic acid 57% (Merck 341), H3PO2 50% (Fluka 9421), benzylamine (Fluka 13180)\",\n        \"synthesis_product\": \"Orange plate crystals\",\n        \"synthesis_description\": \"To prepare C6H5CH2NH3I, treat benzylamine with aq.HI 57% in the presence of H3PO2 and recrystallize the precipitate from acetonitrile.\\r\\n\\r\\nTreat C6H5CH2NH3I and PbI2 in molar ratio 2:1 in CH3CN or DMF to obtain small crystals. \\r\\n\\r\\nDissolve C6H5CH2NH2 (107 mg, 1 mmol) and PbO (111.5 mg, 0.5 mmol) in aq. HI (57%) in the presence of H3PO2 at reflux temperature to obtain large crystals. \\r\\n\\r\\nSlowly cool the solution and obtain the crystals several hours later, filter and dry in air.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Collect on a Crystal Logic dual goniometer using graphite monochromated MoKa radiation. Unit cell dimensions were determined and refined by using the angular setting of 24 automatically centered reflections in the range 11\\u00b0 < 29 < 24\\u00b0. Intensity data were recorded using a Theta-2theta scan. Refer to page 1406 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1515/ncrs-1999-0318\",\n        \"dataset_ID\": 229,\n        \"id\": 13,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead chloride\",\n        \"formula\": \"C14H20N2PbCl4\",\n        \"group\": \"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal structure of bis(benzylammonium) lead tetrachloride,(C7H7NH3)2PbCl4\",\n        \"journal\": \"Zeitschrift f\\u00fcr Kristallographie - New Crystal Structures\",\n        \"vol\": \"214\",\n        \"pages_start\": \"331\",\n        \"pages_end\": \"332\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"Lead chloride, benzylamine (Merck), HCl, DMF\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Benzyl ammonium chloride was prepared by adding a stoichiometric amount of 37% concentrated HCl to benzylamine. Then, the solvent from a dimethylformamide solution of lead chloride and benzyl ammonium chloride (1:2) was slowly evaporated.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Nicolet P3, Wyckoff diffractometer with Mo Ka radiation (0.71073 \\u00c0)\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1515/ncrs-1999-0319\",\n        \"dataset_ID\": 230,\n        \"id\": 14,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead chloride\",\n        \"formula\": \"C22H24N2PbCl4\",\n        \"group\": \"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal structure of bis(2-naphthylmethylammonium) lead tetra-chloride, (C11H9NH3)2PbCl4\",\n        \"journal\": \"Zeitschrift f\\u00fcr Kristallographie - New Crystal Structures\",\n        \"vol\": \"214\",\n        \"pages_start\": \"333\",\n        \"pages_end\": \"334\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"Lead chloride, 2-naphthylmethyl-amine, HCl, DMF\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Slowly evaporate the solvent from a solution of lead chloride and 2-naphthylmethyl-ammonium chloride with the ratio 1:2 in dimethylformamide.\\r\\n\\r\\nPrepare 2-naphthylmethyl-amine (NMA) according to the procedure outlined in [1] and [2]. Add a stoichiometric amount of 37% concentrated HCl to prepare the adjunct hydrochloride salt.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Nicolet P3, Wyckoff diffractometer with Mo Ka radiation (0.71073 \\u00c2)\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 231,\n        \"id\": 15,\n        \"compound_name\": \"Bis(Butylammonium) germanium iodide\",\n        \"formula\": \"C8H24N2GeI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodogermanate(II), (C4H9NH3)2GeI4, (C4H12N)2GeI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"GeI4, Germanium iodide\",\n        \"iupac\": \"bis(butane-1-aminium) germanium(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"GeI4, HI, H3PO2, C4H9NH2\",\n        \"synthesis_product\": \"Bright orange sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.709 g (1.22 mmol) of GeI4 in 50 mL 3 M HI solution at 80 \\u00b0C. Raise temperature of the solution to 98 \\u00b0C and add 4 mL concentrated (50 wt %) aqueous H3PO2 solution. Allow the reduction of GeI4 to GeI2 to proceed for approximately 4 h, then add a solution of 0.491 g (2.44 mmol) of (C4H9NH2).HI in 3 mL of concentrated (57 wt %) aqueous HI, producing a yellow solution. Allow the resulting solution to sit at 80 \\u00b0C in flowing argon until approximately 50% of the solution had evaporated and then slowly (2-5 \\u00b0C/h) cool to -10 \\u00b0C. Filter out the crystals under flowing argon and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pcmn\",\n        \"extraction_method\": \"Manual entry, Table 1\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 232,\n        \"id\": 16,\n        \"compound_name\": \"Bis(Butylammonium) tin iodide\",\n        \"formula\": \"C8H24N2SnI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodostannate(II), (C4H9NH3)2SnI4, (C4H12N)2SnI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"SnI2, HI, C4H9NH2\",\n        \"synthesis_product\": \"Dark red sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.481 g (1.29 mmol) of SnI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 \\u00b0C. In a separate tube, dissolve 2.58 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 \\u00b0C/h from 90 to -10 \\u00b0C, filter the crystals formed under argon or nitrogen and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Select suitable single crystals in an argon-filled drybox (<1 ppm O2 and H2O) under a microscope and seal in quartz capillaries. Collect data at room temperature on an Enraf-Nonius CAD4 diffractometer with graphite-monochromatized Mo Ka radiation. Obtain unitcell parameters and the crystal orientation matrix by a least-squares fit of 25 reflections with 18\\u00b0 < 2\\u03b8 < 30\\u00b0. Monitor intensity control reflections every 5000s during the data collection. Little to no degradation was observed for the compounds. Use the NRCVAX 386 PC version program for structural solution and refinement.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manual entry, Table 1\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 233,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C4H9NH2\",\n        \"synthesis_product\": \"Orange-yellow sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.534 g (1.16 mmol) of PbI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 \\u00b0C. In a separate tube, dissolve 2.32 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 \\u00b0C/h from 90 to -10 \\u00b0C, filter the crystals formed under argon or nitrogen and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Select suitable single crystals in an argon-filled drybox (<1 ppm O2 and H2O) under a microscope and seal in quartz capillaries. Collect data at room temperature on an Enraf-Nonius CAD4 diffractometer with graphite-monochromatized Mo Ka radiation. Obtain unitcell parameters and the crystal orientation matrix by a least-squares fit of 25 reflections with 18\\u00b0 < 2\\u03b8 < 30\\u00b0. Monitor intensity control reflections every 5000s during the data collection. Little to no degradation was observed for the compounds. Use the NRCVAX 386 PC version program for structural solution and refinement.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manual entry, Table 1\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 234,\n        \"id\": 18,\n        \"compound_name\": \"Bis(aminoethyl)-thiophene lead bromide\",\n        \"formula\": \"C8H16N2SPbBr4\",\n        \"group\": \"2,5-bis(aminoethyl)-thiophene tetrabromoplumbate(II), AE1TPbBr4, C8H16SN2PbBr4\",\n        \"organic\": \"C8H16N2S\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,5-bis(aminoethyl)-thiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 235,\n        \"id\": 19,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead bromide\",\n        \"formula\": \"C12H18N2S2PbBr4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrabromoplumbate(II), AE2TPbBr4, (AEBT)PbBr4, AEBTPbBr4, C12H18S2N2PbBr4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 236,\n        \"id\": 20,\n        \"compound_name\": \"Bis(aminoethyl)-terthiophene lead bromide\",\n        \"formula\": \"C16H20N2S3PbBr4\",\n        \"group\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrabromoplumbate(II), AE3TPbBr4, (AE3T)PbBr4, C16H20S3N2PbBr4\",\n        \"organic\": \"C16H20N2S3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 237,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 238,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author, HSE06+SOC\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 239,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 240,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author, HSE06+SOC\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 241,\n        \"id\": 23,\n        \"compound_name\": \"Bis(aminoethyl)-quinquethiophene lead bromide\",\n        \"formula\": \"C24H24N2S5PbBr4\",\n        \"group\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrabromoplumbate(II), AE5TPbBr4, C24H24S5N2PbBr4\",\n        \"organic\": \"C24H24N2S5\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 242,\n        \"id\": 25,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead bromide\",\n        \"formula\": \"C30H28N2PbBr4\",\n        \"group\": \"Anthracenidemethylaminium tetrabromoplumbate(II), AMA2PbBr4, (C15H11NH3)2PbBr4, (C15H14N)2PbBr4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 243,\n        \"id\": 26,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead iodide\",\n        \"formula\": \"C30H28N2PbI4\",\n        \"group\": \"anthracenidemethylaminium tetraiodoplumbate(II), AMA2PbI4, (C15H11NH3)2PbI4, (C15H14N)2PbI4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 244,\n        \"id\": 27,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead iodide\",\n        \"formula\": \"C22H24N2PbI4\",\n        \"group\": \"Bis(1-(2-naphthyl)methylaminium) tetraiodoplumbate(II), NMA2PbI4, (C11H9NH3)2PbI4, (C11H12N)2PbI4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 245,\n        \"id\": 28,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead bromide\",\n        \"formula\": \"C38H32N2PbBr4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetrabromoplumbate(II), (TMA)2PbBr4, (C18H11CH2NH3)2PbBr4, (C19H16N)2PbBr4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 246,\n        \"id\": 29,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead iodide\",\n        \"formula\": \"C38H32N2PbI4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetraiodoplumbate(II), (TMA)2PbI4, (C18H11CH2NH3)2PbI4, (C19H16N)2PbI4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 247,\n        \"id\": 30,\n        \"compound_name\": \"Bis(aminoethyl)-thiophene lead chloride\",\n        \"formula\": \"C8H16N2SPbCl4\",\n        \"group\": \"2,5-bis(aminoethyl)-thiophene tetrachloroplumbate(II), AE1TPbCl4, (AET)PbCl4, AETPbCl4, C8H16SN2PbCl4\",\n        \"organic\": \"C8H16N2S\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,5-bis(aminoethyl)-thiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 248,\n        \"id\": 31,\n        \"compound_name\": \"Bis(aminoethyl)-thiophene lead iodide\",\n        \"formula\": \"C8H16N2SPbI4\",\n        \"group\": \"2,5-bis(aminoethyl)-thiophene tetraiodoplumbate(II), AE1TPbI4, (AET)PbI4, AETPbI4, C8H16SN2PbI4\",\n        \"organic\": \"C8H16N2S\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,5-bis(aminoethyl)-thiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 249,\n        \"id\": 32,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead chloride\",\n        \"formula\": \"C12H18N2S2PbCl4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrachloroplumbate(II), AE2TPbCl4, (AEDT)PbCl4, AEDTPbCl4, C12H18S2N2PbCl4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 250,\n        \"id\": 33,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead iodide\",\n        \"formula\": \"C12H18N2S2PbI4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 251,\n        \"id\": 34,\n        \"compound_name\": \"Bis(aminoethyl)-terthiophene lead chloride\",\n        \"formula\": \"C16H20N2S3PbCl4\",\n        \"group\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrachloroplumbate(II), AE3TPbCl4, (AETT)PbCl4, AETTPbCl4, C16H20S3N2PbCl4\",\n        \"organic\": \"C16H20N2S3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 252,\n        \"id\": 35,\n        \"compound_name\": \"Bis(aminoethyl)-terthiophene lead iodide\",\n        \"formula\": \"C16H20N2S3PbI4\",\n        \"group\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetraiodoplumbate(II), AE3TPbI4, (AETT)PbI4, AETTPbI4, C16H20S3N2PbI4\",\n        \"organic\": \"C16H20N2S3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 253,\n        \"id\": 36,\n        \"compound_name\": \"Bis(aminoethyl)-quinquethiophene lead chloride\",\n        \"formula\": \"C24H24N2S5PbCl4\",\n        \"group\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrachloroplumbate(II), AE5TPbCl4, (AE5T)PbCl4, C24H24S5N2PbCl4\",\n        \"organic\": \"C24H24N2S5\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 254,\n        \"id\": 37,\n        \"compound_name\": \"Bis(aminoethyl)-quinquethiophene lead iodide\",\n        \"formula\": \"C24H24N2S5PbI4\",\n        \"group\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetraiodoplumbate(II), AE5TPbI4, (AE5T)PbI4, C24H24S5N2PbI4\",\n        \"organic\": \"C24H24N2S5\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"with spin-orbit coupling\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 265,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",\n        \"synthesis_product\": \"Orange MAPbBr3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the orange crystals.\",\n        \"experimental_method\": \"temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No experimental details reported. Refer to Page 6374 Table I.\",\n        \"physical_property\": \">236.9\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Pm3m\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 266,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",\n        \"synthesis_product\": \"Orange MAPbBr3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the orange crystals.\",\n        \"experimental_method\": \"temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No experimental details reported. Refer to Page 6374 Table I.\",\n        \"physical_property\": \">155.1\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"I4/mcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 267,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",\n        \"synthesis_product\": \"Orange MAPbBr3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the orange crystals.\",\n        \"experimental_method\": \"temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No experimental details reported. Refer to Page 6374 Table I.\",\n        \"physical_property\": \">149.5\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"P4/mmm\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 268,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",\n        \"synthesis_product\": \"Orange MAPbBr3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the orange crystals.\",\n        \"experimental_method\": \"temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No experimental details reported. Refer to Page 6374 Table I.\",\n        \"physical_property\": \"<144.5\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 269,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00\\u00b0C to 40\\u00b0C to obtain the black crystals.\",\n        \"experimental_method\": \"temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No experimental details reported. Refer to Page 6374 Table I.\",\n        \"physical_property\": \">327.4\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Pm3m\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 270,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00\\u00b0C to 40\\u00b0C to obtain the black crystals.\",\n        \"experimental_method\": \"temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No experimental details reported. Refer to Page 6374 Table I.\",\n        \"physical_property\": \">162.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"I4/mcm\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 271,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00\\u00b0C to 40\\u00b0C to obtain the black crystals.\",\n        \"experimental_method\": \"temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No experimental details reported. Refer to Page 6374 Table I.\",\n        \"physical_property\": \"<162.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 272,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"[AE2T].2HI (synthesized), BiI3, AgI, hydriodic acid (58 wt. % in H2O)\",\n        \"synthesis_product\": \"dark red [AE2T]2AgBiI8 single crystals\",\n        \"synthesis_description\": \"Stoichiometric quantities of [AE2T].2HI (7.8 \\u03bcmoles), BiI3 (3.9 \\u03bcmoles) and AgI (3.9 \\u03bcmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 2 ml deionized water at 100\\u00b0 C for 30 min. The solution was then slowly cooled to room temperature over 60 hrs. The as-obtained dark red crystals (~ 82 % yield) were filtered, washed with copious amounts of diethyl ether, dried in vacuum and stored in a N2 glove box for further characterization.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) using a Bruker APEX II CCD diffractometer operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 273,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"[AE2T].2HI (synthesized), BiI3, AgI, hydriodic acid (58 wt. % in H2O)\",\n        \"synthesis_product\": \"dark red [AE2T]2AgBiI8 single crystals\",\n        \"synthesis_description\": \"Stoichiometric quantities of [AE2T].2HI (7.8 \\u03bcmoles), BiI3 (3.9 \\u03bcmoles) and AgI (3.9 \\u03bcmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 2 ml deionized water at 100\\u00b0 C for 30 min. The solution was then slowly cooled to room temperature over 60 hrs. The as-obtained dark red crystals (~ 82 % yield) were filtered, washed with copious amounts of diethyl ether, dried in vacuum and stored in a N2 glove box for further characterization.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) using a Bruker APEX II CCD diffractometer operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 274,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"[AE2T].2HI, BiI3, Ag,  hydriodic acid (58 wt. % in H2O), anhydrous dimethylformamide\",\n        \"synthesis_product\": \"[AE2T]2AgBiI thin film\",\n        \"synthesis_description\": \"Stoichiometric amounts of [AE2T].2HI (0.024 mmoles), BiI3 (0.012 mmoles) and AgI (0.012 mmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 4 ml deionized water at 100\\u00b0 C for 30 min. The solution was cooled to room temperature and the resulting dark red precipitate was collected by centrifugation, washed with diethyl ether, and dried in vacuum. The solid powder was dissolved in 80 \\u03bcL of anhydrous dimethylformamide. 40 \\u03bcL of the solution was spin-coated on pre-cleaned glass substrates at a spin speed of 1500 RPM for 30 s, and annealed at 150\\u00b0 C on a hot plate for 10 min in a N2-filled glove box.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Shimadzu UV-3600 UV\\u2212vis-NIR spectrophotometer\",\n        \"physical_property\": \"78.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 275,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"[AE2T].2HI, BiI3, Ag, hydriodic acid (58 wt. % in H2O), anhydrous dimethylformamide\",\n        \"synthesis_product\": \"[AE2T]2AgBiI thin film\",\n        \"synthesis_description\": \"Stoichiometric amounts of [AE2T].2HI (0.024 mmoles), BiI3 (0.012 mmoles) and AgI (0.012 mmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 4 ml deionized water at 100\\u00b0 C for 30 min. The solution was cooled to room temperature and the resulting dark red precipitate was collected by centrifugation, washed with diethyl ether, and dried in vacuum. The solid powder was dissolved in 80 \\u03bcL of anhydrous dimethylformamide. 40 \\u03bcL of the solution was spin-coated on pre-cleaned glass substrates at a spin speed of 1500 RPM for 30 s, and annealed at 150\\u00b0 C on a hot plate for 10 min in a N2-filled glove box.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Shimadzu UV-3600 UV\\u2212vis-NIR spectrophotometer\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 277,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"transient absorption\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"[AE2T].2HI, BiI3, Ag, hydriodic acid (58 wt. % in H2O), anhydrous dimethylformamide\",\n        \"synthesis_product\": \"[AE2T]2AgBiI thin film\",\n        \"synthesis_description\": \"Stoichiometric amounts of [AE2T].2HI (0.024 mmoles), BiI3 (0.012 mmoles) and AgI (0.012 mmoles) were dissolved in a mixture of 0.5 ml hydriodic acid (58 wt. % in H2O) and 4 ml deionized water at 100\\u00b0 C for 30 min. The solution was cooled to room temperature and the resulting dark red precipitate was collected by centrifugation, washed with diethyl ether, and dried in vacuum. The solid powder was dissolved in 80 \\u03bcL of anhydrous dimethylformamide. 40 \\u03bcL of the solution was spin-coated on pre-cleaned glass substrates at a spin speed of 1500 RPM for 30 s, and annealed at 150\\u00b0 C on a hot plate for 10 min in a N2-filled glove box.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"335.0\",\n        \"unit\": \"nm\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 279,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"cm^{-1}\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"2nd variational non-self-consistent SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"0.025 eV\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"absorption_soc_Gaussian_0.1_x_x\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 282,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"0.005 eV/Angstrom\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 287,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"density of states\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"2nd variational non-self-consistent SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"0.05 eV\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 296,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"projected density of states\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"2nd variational non-self-consistent SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"0.05 eV\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Ag\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 301,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"density of states\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"2nd variational non-self-consistent SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"0.05\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Ag\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 312,\n        \"id\": 46,\n        \"compound_name\": \"Cesium silver bismuth chloride\",\n        \"formula\": \"Cs2AgBiCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) \\u00b5-dichloro trichlorobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            2\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"density of states\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"30x30x30\",\n        \"level_of_relativity\": \"2nd variational non-self-consistent SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"0.05 eV\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 313,\n        \"id\": 46,\n        \"compound_name\": \"Cesium silver bismuth chloride\",\n        \"formula\": \"Cs2AgBiCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) \\u00b5-dichloro trichlorobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            2\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"projected density of states\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"30x30x30\",\n        \"level_of_relativity\": \"2nd variational non-self-consistent SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"0.05 eV\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"Ag\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevApplied.10.041001\",\n        \"dataset_ID\": 314,\n        \"id\": 46,\n        \"compound_name\": \"Cesium silver bismuth chloride\",\n        \"formula\": \"Cs2AgBiCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) \\u00b5-dichloro trichlorobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            2\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic Defect Properties in Halide Double Perovskites for Optoelectronic Applications\",\n        \"journal\": \"Physical Review Applied\",\n        \"vol\": \"10\",\n        \"pages_start\": \"041001-1\",\n        \"pages_end\": \"041001-7\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 316,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            317\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"FHI-aims tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 317,\n        \"id\": 45,\n        \"compound_name\": \"5,5'diylbis(amino-ethyl)-[2,2'-bithiophene] silver bismuth iodide\",\n        \"formula\": \"C12H16N2S2AgBiI8\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoargentate(I) \\u00b5-diiodo tetraiodobismuthate(III), (AE2T)2AgBiI8, (C12H16S2N2)AgBiI8\",\n        \"organic\": \"C12H16N2S2\",\n        \"inorganic\": \"AgBiI8, Silver bismuth iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene silver(I) bismuth(III) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            316\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"FHI-aims tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 322,\n        \"id\": 46,\n        \"compound_name\": \"Cesium silver bismuth chloride\",\n        \"formula\": \"Cs2AgBiCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) \\u00b5-dichloro trichlorobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            2\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"8*8*8\",\n        \"level_of_relativity\": \"atomic ZORA with SOC\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 330,\n        \"id\": 46,\n        \"compound_name\": \"Cesium silver bismuth chloride\",\n        \"formula\": \"Cs2AgBiCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) \\u00b5-dichloro trichlorobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            2\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"Wien2K\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"1000\",\n        \"level_of_relativity\": \"Koelling-Harmon approximation + SOC\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 332,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 333,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 334,\n        \"id\": 4,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead chloride\",\n        \"formula\": \"C30H28N2PbCl4\",\n        \"group\": \"bis(anthracen-1-ylmethanaminium) tetrachloroplumbate(II), AMA2PbCl4, (C15H11NH3)2PbCl4, (C15H14N)2PbCl4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(anthracen-1-ylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"AMA2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 335,\n        \"id\": 7,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead bromide\",\n        \"formula\": \"C22H24N2PbBr4\",\n        \"group\": \"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"NMA2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"1x4x4\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 336,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"1x4x4\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 337,\n        \"id\": 12,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 338,\n        \"id\": 13,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead chloride\",\n        \"formula\": \"C14H20N2PbCl4\",\n        \"group\": \"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 339,\n        \"id\": 14,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead chloride\",\n        \"formula\": \"C22H24N2PbCl4\",\n        \"group\": \"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"4x4x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 340,\n        \"id\": 18,\n        \"compound_name\": \"Bis(aminoethyl)-thiophene lead bromide\",\n        \"formula\": \"C8H16N2SPbBr4\",\n        \"group\": \"2,5-bis(aminoethyl)-thiophene tetrabromoplumbate(II), AE1TPbBr4, C8H16SN2PbBr4\",\n        \"organic\": \"C8H16N2S\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,5-bis(aminoethyl)-thiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"1x2x2\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 341,\n        \"id\": 19,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead bromide\",\n        \"formula\": \"C12H18N2S2PbBr4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrabromoplumbate(II), AE2TPbBr4, (AEBT)PbBr4, AEBTPbBr4, C12H18S2N2PbBr4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 342,\n        \"id\": 20,\n        \"compound_name\": \"Bis(aminoethyl)-terthiophene lead bromide\",\n        \"formula\": \"C16H20N2S3PbBr4\",\n        \"group\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrabromoplumbate(II), AE3TPbBr4, (AE3T)PbBr4, C16H20S3N2PbBr4\",\n        \"organic\": \"C16H20N2S3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 343,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 345,\n        \"id\": 23,\n        \"compound_name\": \"Bis(aminoethyl)-quinquethiophene lead bromide\",\n        \"formula\": \"C24H24N2S5PbBr4\",\n        \"group\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrabromoplumbate(II), AE5TPbBr4, C24H24S5N2PbBr4\",\n        \"organic\": \"C24H24N2S5\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 346,\n        \"id\": 25,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead bromide\",\n        \"formula\": \"C30H28N2PbBr4\",\n        \"group\": \"Anthracenidemethylaminium tetrabromoplumbate(II), AMA2PbBr4, (C15H11NH3)2PbBr4, (C15H14N)2PbBr4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 347,\n        \"id\": 26,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead iodide\",\n        \"formula\": \"C30H28N2PbI4\",\n        \"group\": \"anthracenidemethylaminium tetraiodoplumbate(II), AMA2PbI4, (C15H11NH3)2PbI4, (C15H14N)2PbI4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 348,\n        \"id\": 27,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead iodide\",\n        \"formula\": \"C22H24N2PbI4\",\n        \"group\": \"Bis(1-(2-naphthyl)methylaminium) tetraiodoplumbate(II), NMA2PbI4, (C11H9NH3)2PbI4, (C11H12N)2PbI4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 349,\n        \"id\": 28,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead bromide\",\n        \"formula\": \"C38H32N2PbBr4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetrabromoplumbate(II), (TMA)2PbBr4, (C18H11CH2NH3)2PbBr4, (C19H16N)2PbBr4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 350,\n        \"id\": 29,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead iodide\",\n        \"formula\": \"C38H32N2PbI4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetraiodoplumbate(II), (TMA)2PbI4, (C18H11CH2NH3)2PbI4, (C19H16N)2PbI4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 351,\n        \"id\": 30,\n        \"compound_name\": \"Bis(aminoethyl)-thiophene lead chloride\",\n        \"formula\": \"C8H16N2SPbCl4\",\n        \"group\": \"2,5-bis(aminoethyl)-thiophene tetrachloroplumbate(II), AE1TPbCl4, (AET)PbCl4, AETPbCl4, C8H16SN2PbCl4\",\n        \"organic\": \"C8H16N2S\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,5-bis(aminoethyl)-thiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 352,\n        \"id\": 31,\n        \"compound_name\": \"Bis(aminoethyl)-thiophene lead iodide\",\n        \"formula\": \"C8H16N2SPbI4\",\n        \"group\": \"2,5-bis(aminoethyl)-thiophene tetraiodoplumbate(II), AE1TPbI4, (AET)PbI4, AETPbI4, C8H16SN2PbI4\",\n        \"organic\": \"C8H16N2S\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,5-bis(aminoethyl)-thiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 353,\n        \"id\": 32,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead chloride\",\n        \"formula\": \"C12H18N2S2PbCl4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetrachloroplumbate(II), AE2TPbCl4, (AEDT)PbCl4, AEDTPbCl4, C12H18S2N2PbCl4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 354,\n        \"id\": 33,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead iodide\",\n        \"formula\": \"C12H18N2S2PbI4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 355,\n        \"id\": 34,\n        \"compound_name\": \"Bis(aminoethyl)-terthiophene lead chloride\",\n        \"formula\": \"C16H20N2S3PbCl4\",\n        \"group\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetrachloroplumbate(II), AE3TPbCl4, (AETT)PbCl4, AETTPbCl4, C16H20S3N2PbCl4\",\n        \"organic\": \"C16H20N2S3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 356,\n        \"id\": 35,\n        \"compound_name\": \"Bis(aminoethyl)-terthiophene lead iodide\",\n        \"formula\": \"C16H20N2S3PbI4\",\n        \"group\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene tetraiodoplumbate(II), AE3TPbI4, (AETT)PbI4, AETTPbI4, C16H20S3N2PbI4\",\n        \"organic\": \"C16H20N2S3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5''-bis(aminoethyl)-2,2':5',2''-terthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 357,\n        \"id\": 36,\n        \"compound_name\": \"Bis(aminoethyl)-quinquethiophene lead chloride\",\n        \"formula\": \"C24H24N2S5PbCl4\",\n        \"group\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetrachloroplumbate(II), AE5TPbCl4, (AE5T)PbCl4, C24H24S5N2PbCl4\",\n        \"organic\": \"C24H24N2S5\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 358,\n        \"id\": 37,\n        \"compound_name\": \"Bis(aminoethyl)-quinquethiophene lead iodide\",\n        \"formula\": \"C24H24N2S5PbI4\",\n        \"group\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene tetraiodoplumbate(II), AE5TPbI4, (AE5T)PbI4, C24H24S5N2PbI4\",\n        \"organic\": \"C24H24N2S5\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5''''-bis(aminoethyl)-2,2':5',2'':5'',2''':5''',2''''-quinquethiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 359,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 360,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"-\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 365,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit-coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Geometry optimized with PBE\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02909\",\n        \"dataset_ID\": 366,\n        \"id\": 33,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead iodide\",\n        \"formula\": \"C12H18N2S2PbI4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit-coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Direct-Bandgap 2D Silver-Bismuth Iodide Double Perovskite: The Structure-Directing Influence of an Oligothiophene Spacer Cation.\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"7955\",\n        \"pages_end\": \"7964\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ee43822h\",\n        \"dataset_ID\": 367,\n        \"id\": 38,\n        \"compound_name\": \"Cesium lead iodide\",\n        \"formula\": \"CsPbI3\",\n        \"group\": \"cesium lead iodide, cesium triiodoplumbate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            516,\n            517,\n            518,\n            519,\n            520,\n            521,\n            522\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1957\n        ],\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formamidinium lead trihalide: a broadly tunable perovskite for efficient planar heterojunction solar cells\",\n        \"journal\": \"Energy & Environmental Science\",\n        \"vol\": \"7\",\n        \"pages_start\": \"982\",\n        \"pages_end\": \"988\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"CsI, PbI2, dimethyl sulfoxide\",\n        \"synthesis_product\": \"CsPbI3 film\",\n        \"synthesis_description\": \"Equimolar amounts of CsI and PbI2 were dissolved in dimethyl sulfoxide at 0.6M, in a nitrogen-filled glovebox. Films were spin-coated at 2000rpm and annealed at 100 degrees C for 5 minutes in the glovebox.\",\n        \"experimental_method\": \"Optical absorption\",\n        \"experimental_description\": \"Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\\r\\nEstimated band gap was determined from the extrapolation of the linear region to the energy-axis intercept in the direct bandgap Tauc plot.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual entry, page 983 paragraph 5; Fig. 1c.; ESI: 5. Tauc plot\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ee43822h\",\n        \"dataset_ID\": 368,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1959\n        ],\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formamidinium lead trihalide: a broadly tunable perovskite for efficient planar heterojunction solar cells\",\n        \"journal\": \"Energy & Environmental Science\",\n        \"vol\": \"7\",\n        \"pages_start\": \"982\",\n        \"pages_end\": \"988\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"FAI, PbI2, N,N-dimethylformamide (DMF)\",\n        \"synthesis_product\": \"FAPbI3 film\",\n        \"synthesis_description\": \"FAI and PbI2 were dissolved in anhydrous DMF in a 1:1 molar ratio, at 0.88M. 60\\u00b5l of hydroiodic acid (57%w/w) was added to 1ml of the solution. The FAPbI3 precursor was diluted down to 0.55M with DMF. The precursor solution was spin-coated and annealed on glass in a nitrogen-filled glovebox at 170\\u00b0C for 25 minutes.\",\n        \"experimental_method\": \"optical absorption\",\n        \"experimental_description\": \"Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere. Estimated band gap was determined from the extrapolation of the linear region to the energy-axis intercept in the direct bandgap Tauc plot.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual entry, page 983 paragraph 5; Fig. 1c.; ESI: 5. Tauc plot\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 369,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 Single crystal\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Agilent Supernova diffractometer (Mo K\\u03b1, \\u03bb = 0.71073 \\u00c5) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibriate for at least one hour after the phase transition to obtain a higher quality dataset. Manual indexing routine. Refer to Page 9304 Section 3.4 Paragraph 2; SI Table S3.\",\n        \"physical_property\": \"343.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 370,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 Single crystal\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Agilent Supernova diffractometer (Mo K\\u03b1, \\u03bb = 0.71073 \\u00c5) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibrate for at least one hour after the phase transition to obtain a higher quality dataset. Manual indexing routine. Refer to Page 9304 Section 3.4 Paragraph 2; SI Table S5.\",\n        \"physical_property\": \"343.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5ta01125f\",\n        \"dataset_ID\": 371,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A combined single crystal neutron/X-ray diffraction and solid-state nuclear magnetic resonance study of the hybrid perovskites CH3NH3PbX3 (X = I, Br and Cl)\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"3\",\n        \"pages_start\": \"9298\",\n        \"pages_end\": \"9307\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), concentrated aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 Single crystal\",\n        \"synthesis_description\": \"Precipitate polycrystalline MAPbI3 from a halogenated acid solution using the method of [1]. Dissolve 1.88 g of lead(II) acetate in 40 ml concentrated to 57 wt% HI aqueous solution warmed (~90 \\u00b0C) in a water bath. Then add another 2 ml of HI solution with 0.45 g CH3NH2. Crystallize by cooling the solution from 90 \\u00b0C to room temperature over 3 hours. Wash product with acetone and dry overnight at 100 \\u00b0C in a vacuum oven. Obtain larger crystals via slow cooling from 90 to 50 \\u00b0C over 3 days.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Agilent Supernova diffractometer (Mo K\\u03b1, \\u03bb = 0.71073 \\u00c5) fitted with an Atlas detector, using Mo radiation. Allow crystal of MAPbI3 to equilibrate for at least one hour after the phase transition to obtain a higher quality dataset. Manual indexing routine. Refer to Page 9304 Section 3.4 Paragraph 2; SI Table S5.\",\n        \"physical_property\": \"343.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 372,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"CASTEP 50\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-GGA\",\n        \"k_point_grid\": \"4x4x4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 373,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"CASTEP 50\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-GGA\",\n        \"k_point_grid\": \"4x4x4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 374,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"CASTEP 50\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-GGA\",\n        \"k_point_grid\": \"4x4x4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 375,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"CASTEP 50\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-GGA\",\n        \"k_point_grid\": \"4x4x4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C5CP02605A\",\n        \"dataset_ID\": 376,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Characterization of an abnormal photoluminescence behavior upon crystal-phase transition of perovskite CH3NH3PbI3\",\n        \"journal\": \"Physical Chemistry Chemical Physics\",\n        \"vol\": \"17\",\n        \"pages_start\": \"16405\",\n        \"pages_end\": \"16411\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Laser excitation\",\n        \"experimental_description\": \"Steady-state and time-resolved PL spectra were measured using an Edinburgh FLS920 spectroscopy system using laser excitation at 405 nm. PL peak is due to NBE emission, i.e., free exciton recombination due to the large binding energy at low temperature range.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry, results and discussion paragraph 2; Fig. 2(a) Peak_T\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 377,\n        \"id\": 2,\n        \"compound_name\": \"Bis(phenylethylammonium) lead chloride\",\n        \"formula\": \"C16H24N2PbCl4\",\n        \"group\": \"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PEA)2PbCl4, (C8H12N)2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            11\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 378,\n        \"id\": 6,\n        \"compound_name\": \"Bis(2-(2-naphthyl)ethanammonium) lead iodide\",\n        \"formula\": \"C24H28N2PbI4\",\n        \"group\": \"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(2-naphthyl)ethane-1-aminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"NEA2PbI4, (C24H28N2)PbI4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            14\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NEA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin-film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He\\u2212Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pn\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 379,\n        \"id\": 7,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead bromide\",\n        \"formula\": \"C22H24N2PbBr4\",\n        \"group\": \"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"NMA2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            12\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NMA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin-film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He\\u2212Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 380,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            7\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 381,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            9\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 382,\n        \"id\": 10,\n        \"compound_name\": \"Bis(2-(2-naphtyl)ethanammonium) lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            15\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NEA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 383,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            10\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 384,\n        \"id\": 12,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            6\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 385,\n        \"id\": 13,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead chloride\",\n        \"formula\": \"C14H20N2PbCl4\",\n        \"group\": \"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            8\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 386,\n        \"id\": 14,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead chloride\",\n        \"formula\": \"C22H24N2PbCl4\",\n        \"group\": \"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            13\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NMA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The photoluminescence spectra were measured using a Horiba-Jobi-Yvon LabRAM ARAMIS system, with a 325 nm He-Cd laser excitation. The laser beam was collimated and focused through a 40X UV objective onto the sample surface at room temperature. Refer to figure 5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer (Figure 5)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 387,\n        \"id\": 15,\n        \"compound_name\": \"Bis(Butylammonium) germanium iodide\",\n        \"formula\": \"C8H24N2GeI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodogermanate(II), (C4H9NH3)2GeI4, (C4H12N)2GeI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"GeI4, Germanium iodide\",\n        \"iupac\": \"bis(butane-1-aminium) germanium(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            16\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"GeI4, HI, H3PO2, C4H9NH2\",\n        \"synthesis_product\": \"Bright orange sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.709 g (1.22 mmol) of GeI4 in 50 mL 3 M HI solution at 80 \\u00b0C. Raise the temperature of the solution to 98 \\u00b0C and add 4 mL concentrated (50 wt %) aqueous H3PO2 solution. Allow the reduction of GeI4 to GeI2 to proceed for approximately 4 h, then add a solution of 0.491 g (2.44 mmol) of (C4H9NH2).HI in 3 mL of concentrated (57 wt %) aqueous HI, producing a yellow solution. Allow the resulting solution to sit at 80 \\u00b0C in flowing argon until approximately 50% of the solution had evaporated and then slowly (2-5 \\u00b0C/h) cool to -10 \\u00b0C. Filter out the crystals under flowing argon and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pcmn\",\n        \"extraction_method\": \"Engauge Digitizer, Figure 5\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 388,\n        \"id\": 16,\n        \"compound_name\": \"Bis(Butylammonium) tin iodide\",\n        \"formula\": \"C8H24N2SnI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodostannate(II), (C4H9NH3)2SnI4, (C4H12N)2SnI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tin(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            17\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"SnI2, HI, C4H9NH2\",\n        \"synthesis_product\": \"Dark red sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.481 g (1.29 mmol) of SnI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 \\u00b0C. In a separate tube, dissolve 2.58 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 \\u00b0C/h from 90 to -10 \\u00b0C, filter the crystals formed under argon or nitrogen and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer, Figure 5\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm9505097\",\n        \"dataset_ID\": 389,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            18\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Crystal Structure, and Optical and Thermal Properties of (C4H9NH3)2MI4 (M = Ge, Sn, Pb)\",\n        \"journal\": \"Chem. Mater.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"791\",\n        \"pages_end\": \"800\",\n        \"year\": \"1996\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C4H9NH2\",\n        \"synthesis_product\": \"Orange-yellow sheetlike crystals\",\n        \"synthesis_description\": \"Grow the crystals under slowly-cooled aqueous hydriodic acid solutions. Perform all synthetic steps and crystal manipulations after synthesis in an inert atmosphere to prevent oxidation.\\r\\n\\r\\nDissolve 0.534 g (1.16 mmol) of PbI2 in 2 mL of concentrated (57 wt %) aqueous HI solvent under flowing argon at 90 \\u00b0C. In a separate tube, dissolve 2.32 mmol of (C4H9NH2).HI in 3 mL of concentrated HI solution and add to the metal halide solution. Ramp the solution temperature at 2 \\u00b0C/h from 90 to -10 \\u00b0C, filter the crystals formed under argon or nitrogen and dry in argon at 80 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Collect the photoluminescence spectra within several hours after the crystals were synthesized, and maintain the samples in an argon-filled cell during measurement to prevent degradation. The photoluminescence spectra were excited by 457.9 nm (2.71 eV) light from an argon ion laser. This light was strongly absorbed by each sample, ensuring that the observed luminescence came from the front side of the samples. The excitation density was below 1 W cm-2. Refer to Page 794 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer, Figure 5\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 393,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HBr, N1-methylethane-1,2-diamine, PbBr2\",\n        \"synthesis_product\": \"Colorless plate-like crystals\",\n        \"synthesis_description\": \"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 \\u02daC. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Emission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1) 2(1) 2(1)\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 394,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            403\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1) 2(1) 2(1)\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 395,\n        \"id\": 48,\n        \"compound_name\": \"N-methylpropane-1,3-diammonium lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylpropane-1,3-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HBr, N1-methylpropane-1,3-diamine, PbBr2\",\n        \"synthesis_product\": \"Pale-yellow crystals\",\n        \"synthesis_description\": \"N1 -methylpropane-1,3-diammonium (N-MPDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylpropane-1,3-diamine (0.5 mL, 4.8 mmol) at 0 \\u02daC. The solvent was removed, and the resulting solid was washed with cold acetone. Finally, the solid was held under reduced pressure for 12 h to obtain (N-MPDA)Br2 as a colorless, crystalline solid. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MPDA)Br2 (0.067 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12 h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Emission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 396,\n        \"id\": 48,\n        \"compound_name\": \"N-methylpropane-1,3-diammonium lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylpropane-1,3-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            400,\n            401\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 397,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HBr, N1-methylethane-1,2-diamine, PbBr2\",\n        \"synthesis_product\": \"Colorless plate-like crystals\",\n        \"synthesis_description\": \"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 \\u02daC. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded in a Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and using monochromated Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1) 2(1) 2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 398,\n        \"id\": 48,\n        \"compound_name\": \"N-methylpropane-1,3-diammonium lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylpropane-1,3-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HBr, N1-methylpropane-1,3-diamine, PbBr2\",\n        \"synthesis_product\": \"Pale-yellow crystals\",\n        \"synthesis_description\": \"N1 -methylpropane-1,3-diammonium (N-MPDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylpropane-1,3-diamine (0.5 mL, 4.8 mmol) at 0 \\u02daC. The solvent was removed, and the resulting solid was washed with cold acetone. Finally, the solid was held under reduced pressure for 12 h to obtain (N-MPDA)Br2 as a colorless, crystalline solid. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MPDA)Br2 (0.067 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12 h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded in a Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and using monochromated Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 400,\n        \"id\": 48,\n        \"compound_name\": \"N-methylpropane-1,3-diammonium lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylpropane-1,3-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            396,\n            401\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 401,\n        \"id\": 48,\n        \"compound_name\": \"N-methylpropane-1,3-diammonium lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylpropane-1,3-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            396,\n            400\n        ],\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 402,\n        \"id\": 48,\n        \"compound_name\": \"N-methylpropane-1,3-diammonium lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N-methylpropane-1,3-diaminium tetrabromoplumbate(II), (N-MPDA)PbBr4, C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylpropane-1,3-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HBr, N1-methylpropane-1,3-diamine, PbBr2\",\n        \"synthesis_product\": \"Pale-yellow crystals\",\n        \"synthesis_description\": \"N1 -methylpropane-1,3-diammonium (N-MPDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylpropane-1,3-diamine (0.5 mL, 4.8 mmol) at 0 \\u02daC. The solvent was removed, and the resulting solid was washed with cold acetone. Finally, the solid was held under reduced pressure for 12 h to obtain (N-MPDA)Br2 as a colorless, crystalline solid. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MPDA)Br2 (0.067 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12 h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Emission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 403,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            394\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1) 2(1) 2(1)\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 405,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Absorption was recorded using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1) 2(1) 2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 407,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HBr, N1-methylethane-1,2-diamine, PbBr2\",\n        \"synthesis_product\": \"Colorless plate-like crystals\",\n        \"synthesis_description\": \"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 \\u02daC. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",\n        \"experimental_method\": \"PLQE measurement using an integrating sphere\",\n        \"experimental_description\": \"Princeton Instruments SpectraPro 500i spectrograph was used to collect the spectra. See supporting information page S3 for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1) 2(1) 2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 408,\n        \"id\": 49,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead chloride\",\n        \"formula\": \"C6H18N2O2PbCl4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            410\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Measured on spin-coated films using an Agilent Cary 6000i spectrometer\\r\\nin transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 409,\n        \"id\": 49,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead chloride\",\n        \"formula\": \"C6H18N2O2PbCl4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            411\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"colorless solid\",\n        \"synthesis_description\": \"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5.5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4].\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 410,\n        \"id\": 49,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead chloride\",\n        \"formula\": \"C6H18N2O2PbCl4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            408\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 411,\n        \"id\": 49,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead chloride\",\n        \"formula\": \"C6H18N2O2PbCl4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            409\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"colorless solid\",\n        \"synthesis_description\": \"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5.5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4].\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 412,\n        \"id\": 49,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead chloride\",\n        \"formula\": \"C6H18N2O2PbCl4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"colorless solid\",\n        \"synthesis_description\": \"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5.5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4].\",\n        \"experimental_method\": \"PLQE measurement using an integrating sphere\",\n        \"experimental_description\": \"Absolute PLQE measurements were performed on powders on glass slides placed in an integrating sphere. Samples were excited using monochromatic light produced by a mercury-arc lamp and a monochromator fiber coupled to the sphere. The spectra of the emitted light and any unabsorbed excitation light were measured using a Princeton Instruments SpectraPro 500i spectrograph fiber-coupled to the sphere. See the supporting information for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 413,\n        \"id\": 49,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead chloride\",\n        \"formula\": \"C6H18N2O2PbCl4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrachloroplumbate(II), (EDBE)PbCl4, C6H18O2N2PbCl4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"Plate-like crystals\",\n        \"synthesis_description\": \"A 20-mL solution of PbCl2 (1.00 g, 3.60 mmol) in 12-M HCl was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5.5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.5 mL, 10.3 mmol) in 12-M HCl. After 10 minutes, the resulting colorless precipitate was filtered through a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.08 g (60.1% yield) (EDBE)[PbCl4]. Crystals suitable for x-ray structure determination were obtained through diffusion of diethyl ether into a 4-mL solution of the product (0.10 g, 0.20 mmol) in 12-M HCl.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 414,\n        \"id\": 50,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead bromide\",\n        \"formula\": \"C6H18N2O2PbBr4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            416\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 415,\n        \"id\": 50,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead bromide\",\n        \"formula\": \"C6H18N2O2PbBr4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            417\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"colorless solid\",\n        \"synthesis_description\": \"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4].\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 416,\n        \"id\": 50,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead bromide\",\n        \"formula\": \"C6H18N2O2PbBr4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            414\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 417,\n        \"id\": 50,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead bromide\",\n        \"formula\": \"C6H18N2O2PbBr4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            415\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"colorless solid\",\n        \"synthesis_description\": \"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4].\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 418,\n        \"id\": 50,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead bromide\",\n        \"formula\": \"C6H18N2O2PbBr4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"colorless solid\",\n        \"synthesis_description\": \"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4].\",\n        \"experimental_method\": \"PLQE measurement using an integrating sphere\",\n        \"experimental_description\": \"Absolute PLQE measurements were performed on powders on glass slides placed in an integrating sphere. Samples were excited using monochromatic light produced by a mercury-arc lamp and a monochromator fiber coupled to the sphere. The spectra of the emitted light and any unabsorbed excitation light were measured using a Princeton Instruments SpectraPro 500i spectrograph fiber-coupled to the sphere. See the supporting information for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 419,\n        \"id\": 50,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead bromide\",\n        \"formula\": \"C6H18N2O2PbBr4\",\n        \"group\": \"2,2'(ethylenedioxy)bis(ethanaminium) tetrabromoplumbate(II), (EDBE)PbBr4, C6H18O2N2PbBr4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"Plate-like colorless crystals\",\n        \"synthesis_description\": \"A 4-mL solution of PbBr2 (1.00 g, 2.72 mmol) in 9-M HBr was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5-mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 9-M HBr. After 10 minutes, the resulting colorless precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The colorless solid was held at reduced pressure for 12 h to afford 1.66 g (90.0% yield) of (EDBE)[PbBr4]. Crystals suitable for x-ray structure determination were obtained through diffusion of diethyl ether into a 2-mL solution of the product (0.20 g, 0.29 mmol) in 9-M HBr.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 420,\n        \"id\": 51,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead iodide\",\n        \"formula\": \"C6H18N2O2PbI4\",\n        \"group\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead iodide\",\n        \"last_update\": \"2022-06-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            422\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 421,\n        \"id\": 51,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead iodide\",\n        \"formula\": \"C6H18N2O2PbI4\",\n        \"group\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead iodide\",\n        \"last_update\": \"2022-06-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            423\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbI2, HI, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"yellow solid\",\n        \"synthesis_description\": \"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4].\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 422,\n        \"id\": 51,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead iodide\",\n        \"formula\": \"C6H18N2O2PbI4\",\n        \"group\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead iodide\",\n        \"last_update\": \"2022-06-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            420\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Measured on spin-coated films using an Agilent Cary 6000i spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 423,\n        \"id\": 51,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead iodide\",\n        \"formula\": \"C6H18N2O2PbI4\",\n        \"group\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead iodide\",\n        \"last_update\": \"2022-06-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            421\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbI2, HI, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"yellow solid\",\n        \"synthesis_description\": \"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4].\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were collected on non-oriented powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 424,\n        \"id\": 51,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead iodide\",\n        \"formula\": \"C6H18N2O2PbI4\",\n        \"group\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead iodide\",\n        \"last_update\": \"2022-06-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbI2, HI, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"yellow solid\",\n        \"synthesis_description\": \"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4].\",\n        \"experimental_method\": \"PLQE measurement using an integrating sphere\",\n        \"experimental_description\": \"Absolute PLQE measurements were performed on powders on glass slides placed in an integrating sphere. Samples were excited using monochromatic light produced by a mercury-arc lamp and a monochromator fiber coupled to the sphere. The spectra of the emitted light and any unabsorbed excitation light were measured using a Princeton Instruments SpectraPro 500i spectrograph fiber-coupled to the sphere. \\r\\nSee the supporting information for details.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja507086b\",\n        \"dataset_ID\": 425,\n        \"id\": 51,\n        \"compound_name\": \"2,2\\u2032(ethylenedioxy)bis(ethylammonium) lead iodide\",\n        \"formula\": \"C6H18N2O2PbI4\",\n        \"group\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) tetraiodoplumbate(II), (EDBE)PbI4, C6H18O2N2PbI4\",\n        \"organic\": \"C6H18N2O2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,2\\u2032(ethylenedioxy)bis(ethanaminium) lead iodide\",\n        \"last_update\": \"2022-06-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intrinsic White-Light Emission from Layered Hybrid Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"13154\",\n        \"pages_end\": \"13157\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"PbI2, HI, 2,2\\u2019-(ethylenedioxy)bis(ethylamine)\",\n        \"synthesis_product\": \"yellow plate-like crystals\",\n        \"synthesis_description\": \"A 6-mL solution of PbI2 (1.00 g, 2.17 mmol) in 8-M HI was added dropwise to a cold (\\u201370 \\u00baC), stirred, 5mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.0 mL, 6.85 mmol) in 8-M HI. After 10 minutes, the resulting yellow precipitate was filtered using a glass frit and washed with cold diethyl ether (5 \\u00d7 5 mL). The yellow solid was held at reduced pressure for 12 h to afford 1.70 g (90.6% yield) of (EDBE)[PbI4]. Crystals suitable for x-ray structure determination were obtained through diffusion of diethyl ether into a 3-mL solution of the product (0.20 g, 0.23 mmol) in 8-M HI.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja411045r\",\n        \"dataset_ID\": 426,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Stokes shift\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Self-Assembly of Broadband White-Light Emitters\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"136\",\n        \"pages_start\": \"1718\",\n        \"pages_end\": \"1721\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HBr, N1-methylethane-1,2-diamine, PbBr2\",\n        \"synthesis_product\": \"Colorless plate-like crystals\",\n        \"synthesis_description\": \"N1 -methylethane-1,2-diammonium (N-MEDA) bromide was synthesized by dropwise addition of 12-M solution of HBr (0.5 mL, 6.0 mmol) to a stirred 5-mL ethanol solution of N1-methylethane-1,2-diamine (0.5 mL, 5.7 mmol) at 0 \\u02daC. The solvent was removed under reduced pressure to obtain (N-MEDA)Br2 as a colorless, highly hygroscopic solid. It was dried for 12 h under vacuum and stored in a desiccator. Then, Solid PbBr2 (0.10 g, 0.27 mmol) and (N-MEDA)Br2 (0.064 g, 0.27 mmol) were combined in 5 mL of 12-M HBr and sonicated for 5 minutes to obtain a clear solution. The crystals of (N-MEDA)PbBr were obtained by diffusion of acetone into this solution over a 12-h period. The crystals were filtered, washed with acetone, and dried under reduced pressure.\",\n        \"experimental_method\": \"UV-vis absorbance + Photoluminescence\",\n        \"experimental_description\": \"Absorption was recorded in reflectance mode using a Shimadzu UV-2600 spectrometer equipped with an integrating sphere.\\r\\nEmission spectra were collected by mounting samples on quartz slides and by using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 427,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            428\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"O.D.\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AE4T*2HCl, PbCl2\",\n        \"synthesis_product\": \"AE4TPbCl4 film on glass or quartz\",\n        \"synthesis_description\": \"Thin film growth by RIR-MAPLE method from a 2 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films annealed in nitrogen at 125 C for 5 min after deposition.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"UV-vis spectra were collected using a Shimadzu UV-3600 spectrophotometer using a blank substrate as reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"UV-vis spectroscopy\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 428,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            427\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AE4T*2HCl, PbCl2\",\n        \"synthesis_product\": \"AE4TPbCl4 film on glass or quartz\",\n        \"synthesis_description\": \"Thin film growth by RIR-MAPLE method from a 2 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films annealed in nitrogen at 125 C for 5 min after deposition.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Steady-state PL spectra were recorded using Edinburgh Instruments FS920 fluorimeter that was equipped with a 450 W xenon arc lamp as the excitation source, and a Peltier-cooled Hamamatsu R2658P photomultiplier tube.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Photoluminescence measurement\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 429,\n        \"id\": 33,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead iodide\",\n        \"formula\": \"C12H18N2S2PbI4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"O.D.\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AE2T*2HI, PbI2\",\n        \"synthesis_product\": \"AE2TPbI4 film on glass or quartz\",\n        \"synthesis_description\": \"Thin film growth by RIR-MAPLE method from a 4 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 150 C for 10 min after deposition.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"UV-vis spectra were collected using a Shimadzu UV-3600 spectrophotometer using a blank substrate as reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"UV-vis spectroscopy\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 430,\n        \"id\": 33,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead iodide\",\n        \"formula\": \"C12H18N2S2PbI4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AE2T*2HI, PbI2\",\n        \"synthesis_product\": \"AE2TPbI4 film on glass or quartz\",\n        \"synthesis_description\": \"Thin film growth by RIR-MAPLE method from a 4 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 150 C for 10 min after deposition.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Steady-state PL spectra were recorded using Edinburgh Instruments FS920 fluorimeter that was equipped with a 450 W xenon arc lamp as the excitation source, and a Peltier-cooled Hamamatsu R2658P photomultiplier tube.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Photoluminescence measurement\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 431,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"O.D.\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AE4T*2HI, PbI2\",\n        \"synthesis_product\": \"AE4TPbI4 film on glass or quartz\",\n        \"synthesis_description\": \"Thin film growth by RIR-MAPLE method from a 4 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 200 C for 30 min after deposition.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"UV-vis spectra were collected using a Shimadzu UV-3600 spectrophotometer using a blank substrate as reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"UV-vis spectroscopy\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9mh00366e\",\n        \"dataset_ID\": 432,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable internal quantum well alignment in rationally designed oligomer-based perovskite films deposited by resonant infrared matrix-assisted pulsed laser evaporation\",\n        \"journal\": \"Mater. Horiz.\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1707\",\n        \"pages_end\": \"1716\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AE4T*2HI, PbI2\",\n        \"synthesis_product\": \"AE2TPbI4 film on glass or quartz\",\n        \"synthesis_description\": \"Thin film growth by RIR-MAPLE method from a 8 mM solution of the precursor salts using a 1:1 vol:vol blend of DMSO and ethylene glycol as the solvent. Films are annealed in nitrogen at 150 C for 10 min after deposition.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Steady-state PL spectra were recorded using Edinburgh Instruments FS920 fluorimeter that was equipped with a 450 W xenon arc lamp as the excitation source, and a Peltier-cooled Hamamatsu R2658P photomultiplier tube.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Photoluminescence measurement\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 433,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            434,\n            435,\n            436,\n            437\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HBr, CH3NH2, Pb(NO3)2\",\n        \"synthesis_product\": \"Partially deuterated MAPbBr3\",\n        \"synthesis_description\": \"Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100\\u00b0C to the concentrated CH3NH2Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Partially N-deuterated samples required for the NMR studies were prepared using D-containing solutions. Refer to Page 413 Experimental.\",\n        \"experimental_method\": \"2H and 14N NMR\",\n        \"experimental_description\": \"Measurements were carried out at 8.48 T with a Nicolet 360NB spectrometer using a broad band (16-58 MHz) variable-temperature 10 mm probe supplied by Nicolet. The 2-H and 14-N frequencies were 55.427 and 26.083 MHz, respectively. Refer to Page 414 Results section Existence of transitions subsection.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 434,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            433,\n            435,\n            436,\n            437\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HCl, CD3NH2, PbCl2\",\n        \"synthesis_product\": \"CD3NH3PbCl3 crystals\",\n        \"synthesis_description\": \"Primarily referenced the methods of [1] and [2]. The synthesis of MAPbBr3 in ref [2] was modified to prepare CD3NH3PbCl3.\",\n        \"experimental_method\": \"2H and 14N NMR\",\n        \"experimental_description\": \"Measurements were carried out at 8.48 T with a Nicolet 360NB spectrometer using a broad band (16-58 MHz) variable-temperature 10 mm probe supplied by Nicolet. The 2-H and 14-N frequencies were 55.427 and 26.083 MHz, respectively. Refer to Page 414 Results section Existence of transitions subsection.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 435,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            433,\n            434,\n            436,\n            437\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HI, CH3NH2, Pb(NO3)2\",\n        \"synthesis_product\": \"Partially deuterated MAPbI3\",\n        \"synthesis_description\": \"Add concentrated HI to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100\\u00b0C to the concentrated CH3NH2I solution. Organic crystals form while dripping in the solution. Cool the solution to not below 40\\u00b0C and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Partially N-deuterated samples required for the NMR studies were prepared using D-containing solutions. Refer to Page 413 Experimental.\",\n        \"experimental_method\": \"2H and 14N NMR\",\n        \"experimental_description\": \"Measurements were carried out at 8.48 T with a Nicolet 360NB spectrometer using a broad band (16-58 MHz) variable-temperature 10 mm probe supplied by Nicolet. The 2-H and 14-N frequencies were 55.427 and 26.083 MHz, respectively. Refer to Page 414 Results section Existence of transitions subsection.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 436,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            433,\n            434,\n            435,\n            437\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HBr, CH3NH2, Pb(NO3)2\",\n        \"synthesis_product\": \"MAPbBr3 Single-crystal\",\n        \"synthesis_description\": \"Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution. Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100\\u00b0C to the concentrated CH3NH3Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum. Yield: 9.5 g.\",\n        \"experimental_method\": \"Adiabatic calorimetry\",\n        \"experimental_description\": \"The heat capacities were measured in an adiabatic calorimeter from 30 to 300 K, using sample masses of 12.8235 g MAPbBr3. Refer to Page 414 Table 1.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"IV to III\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1139/v90-063\",\n        \"dataset_ID\": 437,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            433,\n            434,\n            435,\n            436\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkylammonium lead halides. Part 2. CH3NH3PbX3 (X = Cl, Br, I) perovskites: cuboctahedral halide cages with isotropic cation reorientation\",\n        \"journal\": \"Canadian Journal of Chemistry\",\n        \"vol\": \"68\",\n        \"pages_start\": \"412\",\n        \"pages_end\": \"422\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"HCl, CH3NH2, PbCl2\",\n        \"synthesis_product\": \"MAPbCl3 Single-crystal\",\n        \"synthesis_description\": \"Primarily referenced the methods of [1] and [2]. The synthesis of MAPbBr3 in ref [2] was modified to prepare MAPbCl3.\",\n        \"experimental_method\": \"Adiabatic calorimetry\",\n        \"experimental_description\": \"The heat capacities were measured in an adiabatic calorimeter from 30 to 345 K, using sample masses of 14.6883 g MAPbCl3. Refer to Page 414 Table 1.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"III to II\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/0038-1098(85)90959-7\",\n        \"dataset_ID\": 438,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            439,\n            440\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CATION ROTATION IN METHYLAMMONIUM LEAD HALIDES\",\n        \"journal\": \"Solid State Communications\",\n        \"vol\": \"56\",\n        \"pages_start\": \"581\",\n        \"pages_end\": \"582\",\n        \"year\": \"1985\",\n        \"synthesis_starting_materials\": \"HI, CH3NH2, Pb(NO3)2\",\n        \"synthesis_product\": \"N-deuterated MAPbI3 crystals\",\n        \"synthesis_description\": \"Add concentrated HI to neutralize 20 g of 40% CH3NH2 aqueous solution (D2O-H2O mixture). Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100\\u00b0C to the concentrated CH3NH3I solution. Organic crystals form while dripping in the solution. Cool the solution to not below 40\\u00b0C and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum.\",\n        \"experimental_method\": \"2H and 14N NMR\",\n        \"experimental_description\": \"2H and 14N NMR spectra were recorded at 55.4257 and 26.083 MHz, respectively, on a Nicolet 360 NB spectrometer (B0 = 8.48 T). Refer to Page 581.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"III to II\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/0038-1098(85)90959-7\",\n        \"dataset_ID\": 439,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            438,\n            440\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CATION ROTATION IN METHYLAMMONIUM LEAD HALIDES\",\n        \"journal\": \"Solid State Communications\",\n        \"vol\": \"56\",\n        \"pages_start\": \"581\",\n        \"pages_end\": \"582\",\n        \"year\": \"1985\",\n        \"synthesis_starting_materials\": \"HBr, CH3NH2, Pb(NO3)2\",\n        \"synthesis_product\": \"N-deuterated MAPbBr3 single crystals\",\n        \"synthesis_description\": \"Add concentrated HBr to neutralize 20 g of 40% CH3NH2 aqueous solution (D2O-H2O mixture). Add 7.1 g (0.021 mol) of Pb(NO3)2 solution drop-wise under vigorous stirring at 100\\u00b0C to the concentrated CH3NH3Br solution. Red organic crystals form while dripping in the solution. Cool the solution to room temperature and filter out the crystals. Wash crystals firstly with n-butanol and then with benzene; subsequently dry crystals in vacuum.\",\n        \"experimental_method\": \"2H and 14N NMR\",\n        \"experimental_description\": \"2H and 14N NMR spectra were recorded at 55.4257 and 26.083 MHz, respectively, on a Nicolet 360 NB spectrometer (B0 = 8.48 T). Refer to Page 581.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"III to II\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/0038-1098(85)90959-7\",\n        \"dataset_ID\": 440,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            438,\n            439\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CATION ROTATION IN METHYLAMMONIUM LEAD HALIDES\",\n        \"journal\": \"Solid State Communications\",\n        \"vol\": \"56\",\n        \"pages_start\": \"581\",\n        \"pages_end\": \"582\",\n        \"year\": \"1985\",\n        \"synthesis_starting_materials\": \"Not specified\",\n        \"synthesis_product\": \"MAPbCl3 single crystals\",\n        \"synthesis_description\": \"The procedure mentioned in ref [1] for MAPbBr3 was modified. A D2O-H2O mixture was used to prepare the N-deuterated samples.\",\n        \"experimental_method\": \"2H and 14N NMR\",\n        \"experimental_description\": \"2H and 14N NMR spectra were recorded at 55.4257 and 26.083 MHz, respectively, on a Nicolet 360 NB spectrometer (B0 = 8.48 T). Refer to Page 581.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/0022-3697(90)90021-7\",\n        \"dataset_ID\": 441,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            442,\n            443\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Calorimetric and IR Spectroscopic Studies of Phase Transitions in Methylammonium Trihalogenoplumbates (II)\",\n        \"journal\": \"Journal of Physics and Chemistry of Solids\",\n        \"vol\": \"51\",\n        \"pages_start\": \"1383\",\n        \"pages_end\": \"1395\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"Pb(CH3CO2)2, MACl\",\n        \"synthesis_product\": \"Colorless MAPbCl3 cube-shaped crystals of 1-2 mm from the edge\",\n        \"synthesis_description\": \"Add aqueous solution of Pb(CH3CO2)2 drop by drop to an excess quantity of hot aqueous MACl solution and cool slowly to 5 \\u00b0C.\",\n        \"experimental_method\": \"Adiabatic calorimetry\",\n        \"experimental_description\": \"The heat capacities were measured with a computerized adiabatic calorimeter [1, 2]. The temperature ranges of the measurement were between 13 and 300 K. The mass of the calorimetric sample was 6.0483 g.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/0022-3697(90)90021-7\",\n        \"dataset_ID\": 442,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            441,\n            443\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Calorimetric and IR Spectroscopic Studies of Phase Transitions in Methylammonium Trihalogenoplumbates (II)\",\n        \"journal\": \"Journal of Physics and Chemistry of Solids\",\n        \"vol\": \"51\",\n        \"pages_start\": \"1383\",\n        \"pages_end\": \"1395\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"Pb(CH3CO2)2, MABr\",\n        \"synthesis_product\": \"Orange MAPbBr3 cube-shaped crystals of 1-2 mm\",\n        \"synthesis_description\": \"Add aqueous solution of Pb(CH3CO2)2 drop by drop to an excess quantity of hot aqueous MABr solution and cool slowly to 5 \\u00b0C.\",\n        \"experimental_method\": \"Adiabatic calorimetry\",\n        \"experimental_description\": \"The heat capacities were measured with a computerized adiabatic calorimeter [1, 2]. The temperature ranges of the measurement were between 13 and 300 K. The mass of the calorimetric sample was 8.8810 g.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/0022-3697(90)90021-7\",\n        \"dataset_ID\": 443,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            441,\n            442\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Calorimetric and IR Spectroscopic Studies of Phase Transitions in Methylammonium Trihalogenoplumbates (II)\",\n        \"journal\": \"Journal of Physics and Chemistry of Solids\",\n        \"vol\": \"51\",\n        \"pages_start\": \"1383\",\n        \"pages_end\": \"1395\",\n        \"year\": \"1990\",\n        \"synthesis_starting_materials\": \"Pb(CH3CO2)2, MAI\",\n        \"synthesis_product\": \"Black MAPbI3 cube-shaped crystals of 1-2 mm\",\n        \"synthesis_description\": \"Add aqueous solution of Pb(CH3CO2)2 drop by drop to an excess quantity of hot aqueous MAI solution and cool slowly, keeping temperature above 40 \\u00b0C to prevent crystallization of (MA)3Pb6-2H2O.\",\n        \"experimental_method\": \"Adiabatic calorimetry\",\n        \"experimental_description\": \"The heat capacities were measured with a computerized adiabatic calorimeter [1, 2]. The temperature ranges of the measurement were between 13 and 365 K. The mass of the calorimetric sample was 9.3384 g.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1143/JPSJ.71.1694\",\n        \"dataset_ID\": 444,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Study on Cubic\\u2013Tetragonal Transition of CH3NH3PbI3\",\n        \"journal\": \"Journal of the Physical Society of Japan\",\n        \"vol\": \"71\",\n        \"pages_start\": \"1694\",\n        \"pages_end\": \"1697\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"CH3NH3PbI3, lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",\n        \"synthesis_product\": \"Black and opaque MAPbI3 single crystal\",\n        \"synthesis_description\": \"CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ (by adding a 40% solution of CH3NH2 in water) dissolved in concentrated HI solution. Cool aqueous solution from l00\\u00b0C to not lower than 40\\u00b0C to obtain a black crystal. Crystals of about 1 cm in dimension were obtained. Synthesis using reference [2]\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Cut and polish samples into 0.3mm in diameter. Select a single crystal and mount on an off-centered 4-circle diffractometer (HUBER 424) controlled by MXC (Mac Science). Use cold nitrogen gas flow (Oxford Crysteram) to keep the temperature of the sample within \\u00b10.5 K. Use graphite-monochromated Mo-K\\\\alpha radiation from a rotating anode generator with 50 kV\\u2013250 mA. Refer to Page 1695 Fig. 1.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"doi:10.1016/S0022-4596(03)00352-9\",\n        \"dataset_ID\": 445,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase transitions in the perovskite methylammonium lead bromide, CH3ND3PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"176\",\n        \"pages_start\": \"97\",\n        \"pages_end\": \"104\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"MAPbBr3 Powder\",\n        \"synthesis_description\": \"Samples were prepared following well-described\\r\\nmethods [1,2].\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"X-ray diffraction measurements were performed from 120K to room temperature on samples mounted in 0.1mm diameter capillaries, mounted in an Enraf-Nonius Guinier-Simon camera, using CuKa_1 radiation. Refer to Page 98 Experimental.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 446,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            448,\n            449\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HCl\",\n        \"synthesis_product\": \"Colorless MAPbCl3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbCI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HCl solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the colorless crystals.\",\n        \"experimental_method\": \"Temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No method specified. Refer to Page 6374 Table I.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 448,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            446,\n            449\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HBr\",\n        \"synthesis_product\": \"Orange MAPbBr3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbBr3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in concentrated HBr solution. The aqueous solution was cooled from l00\\u00b0C to room temperature to obtain the orange crystals.\",\n        \"experimental_method\": \"Temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No method specified. Refer to Page 6374 Table I.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"144.5-149.5\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.453467\",\n        \"dataset_ID\": 449,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            446,\n            448\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Dynamic disorder in methylammoniumtrihalogenoplumbates (II) observed by millimeter-wave spectroscopy\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"87\",\n        \"pages_start\": \"6373\",\n        \"pages_end\": \"6378\",\n        \"year\": \"1987\",\n        \"synthesis_starting_materials\": \"lead (II) acetate, CH3NH3+ (by adding a 40% solution of CH3NH2 in water), concentrated HI\",\n        \"synthesis_product\": \"Black MAPbI3 crystals\",\n        \"synthesis_description\": \"CH3NH3PbI3 was synthesized from lead (II) acetate and CH3NH3+ dissolved in a concentrated HI solution. The aqueous solution was cooled from l00\\u00b0C to 40\\u00b0C to obtain the black crystals.\",\n        \"experimental_method\": \"Temperature-dependent Guinier-Simon photograph\",\n        \"experimental_description\": \"No method specified. Refer to Page 6374 Table I.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C5CP02605A\",\n        \"dataset_ID\": 450,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Characterization of an abnormal photoluminescence behavior upon crystal-phase transition of perovskite CH3NH3PbI3\",\n        \"journal\": \"Physical Chemistry Chemical Physics\",\n        \"vol\": \"17\",\n        \"pages_start\": \"16405\",\n        \"pages_end\": \"16411\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Methylamine (40% in methanol), hydroiodic acid (57 wt% in water), PbI2, g-butyrolactone, H2O2, NH4OH, Si wafer\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"React 30 mL of methylamine and 32.3 mL of hydroiodic acid at 0 \\u00b0C for 2 h. Evaporate solvents at 50 \\u00b0C. Wash the yellowish raw CH3NH3I with diethyl ether by stirring the solution for 30min for a total of three times. Recrystallize CH3NH3I from a mixed solvent of diethyl ether and ethanol. Collect the solid and dry at 60 \\u00b0C in a vacuum oven for 24 h. Treat Si wafer with an aqueous solution of H2O2 and NH4OH with a volume ratio of H2O2 : NH4OH : H2O = 1 : 1 : 5 for 30 min. Drop a 40 wt% precursor solution of equimolar CH3NH3I and PbI2 in g-butyrolactone onto the Si wafer to form the MAPbI3 film. Spin-coat at 1500 rpm for 30 s, and then at 2500 rpm for 40 min in air. Upon drying at room temperature, color change indicates the formation of MAPbI3 in the solid state. Anneal the MAPbI3 film in air for 15 min at 100 \\u00b0C.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"No experimental details. Coexistence of the two phases at T from 150 to 130 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"dx.doi.org/10.1021/jz5012109\",\n        \"dataset_ID\": 451,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            452\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ultra-Low Thermal Conductivity in Organic\\u2212Inorganic Hybrid Perovskite CH3NH3PbI3\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"5\",\n        \"pages_start\": \"2488\",\n        \"pages_end\": \"2492\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HI (conc), PbAc2, CH3NH3+\",\n        \"synthesis_product\": \"Black MAPbI3 Crystals\",\n        \"synthesis_description\": \"Precipitate product from a concentrated aqueous solution of hydroiodic acid containing lead(II) acetate and a respective amount of CH3NH3+ solution.\\r\\n\\r\\nThe two ends of the sample holder were held at 55 and 42 \\u00b0C respectively to induce the saturation of the solute at the low temperature part of the solution. After 24 h submillimeter sized crystals appeared in the solution.\",\n        \"experimental_method\": \"Thermocouple: Temperature dependence of thermal conductivity\",\n        \"experimental_description\": \"Conducted for 3 samples. Swept down from 310 K to 25 K. Using a steady-state method using calibrated stainless steel as reference sample (Page 2491 Figure 5). Refer to Page 2489 Figure 4.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"dx.doi.org/10.1021/jz5012109\",\n        \"dataset_ID\": 452,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            451\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ultra-Low Thermal Conductivity in Organic\\u2212Inorganic Hybrid Perovskite CH3NH3PbI3\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"5\",\n        \"pages_start\": \"2488\",\n        \"pages_end\": \"2492\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"HI (conc), PbAc2, CH3NH3+\",\n        \"synthesis_product\": \"Black MAPbI3 Crystals\",\n        \"synthesis_description\": \"Precipitate product from a concentrated aqueous solution of hydroiodic acid containing lead(II) acetate and a respective amount of CH3NH3+ solution.\\r\\n\\r\\nThe two ends of the sample holder were held at 55 and 42 \\u00b0C respectively to induce the saturation of the solute at the low temperature part of the solution. After 24 h submillimeter sized crystals appeared in the solution.\",\n        \"experimental_method\": \"Thermocouple: Temperature dependence of thermal conductivity\",\n        \"experimental_description\": \"Conducted for 3 samples. Swept down from 310 K to 25 K. Using a steady-state method using calibrated stainless steel as reference sample (Page 2491 Figure 5). Refer to Page 2489 Figure 4.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 453,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            454,\n            455\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 Polycrystals\",\n        \"synthesis_description\": \"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 \\u00b0C to 46 \\u00b0C over 6 hours and dry (100 \\u00b0C/10 hours). Maintain solution temperature above 40 \\u00b0C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 \\u00b0C.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Tetragonal/cubic phase transition was investigated using variable temperature powder X-ray diffraction. In situ XRD data were collected in asymmetric reflection mode under a static helium atmosphere on an INEL Equinox 3000 (Inel, Artenay, France) equipped with an XRK-900 reactor chamber (Anton-Paar, Graz, Austria), a curved position sensitive detector (Ine, Artenay, France), a copper Ka source and a Ge-(111) focussing mirror.\\r\\n\\r\\nTwo different heating experiments were conducted. In the first, MAPbI3 was heated to 85 \\u00b0C in five degree steps starting from 25 \\u00b0C, with data collected for 5 minutes at each holding temperature. The second experiment employed a continuous heating ramp at a rate of 1\\u00b0 min^-1 during which 30 measurements of 120 seconds were performed. Each measurement corresponds to a temperature span of 2 \\u00b0C; the final temperature of each measurement was recorded in the measurement file. Five empty sample holder measurements were conducted at room temperature in order to establish the chamber background.\\r\\n\\r\\nRefer to Page 5633 Results and discussion; Page 5634 Figure 4 and Figure 5.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 454,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            453,\n            455\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"Lead(II) acetate (Chemical Reagents, Sigma), aqueous HI, CH3NH2 (40% soluble in water, Merck)\",\n        \"synthesis_product\": \"Black MAPbI3 Polycrystals\",\n        \"synthesis_description\": \"Following method by [1], dissolve 2.5 g of lead(II) acetate in 10 ml of concentrated (57% by weight) aqueous HI contained in a pyrex test tube and heat in a water bath. Add an additional 2 ml of HI solution with 0.597 g of CH3NH2 to the solution. Filter the black precipitate upon cooling from 100 \\u00b0C to 46 \\u00b0C over 6 hours and dry (100 \\u00b0C/10 hours). Maintain solution temperature above 40 \\u00b0C. Black crystals up to 2 mm long were obtained by cooling the solution over 4 days. Crystallization proceeded most rapidly at approximately 70 \\u00b0C.\",\n        \"experimental_method\": \"Differential scanning calorimetry\",\n        \"experimental_description\": \"Differential scanning calorimetry (DSC) was conducted on a Q10 V9.9 Build 303 calorimeter (TA Instruments) at a rate of 5 \\u00b0C min^-1 over a temperature range from 25 \\u00b0C to 200 \\u00b0C under nitrogen. Page 5633 Results and discussion; Page 5635 Figure 6 and Figure 7.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ta10518k\",\n        \"dataset_ID\": 455,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            453,\n            454\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal chemistry of the hybrid perovskite (CH3NH3)PbI3 for solid-state sensitised solar cell applications\",\n        \"journal\": \"Journal of Materials Chemistry\",\n        \"vol\": \"1\",\n        \"pages_start\": \"5628\",\n        \"pages_end\": \"5641\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"HI (Sigma Aldrich), methylamine, PbI2 (99%, Sigma Aldrich), gamma-butyrolactone (Sigma Aldrich)\",\n        \"synthesis_product\": \"Black MAPbI3 Single crystals\",\n        \"synthesis_description\": \"MAPbI3 was synthesized using the method described by [2]. Make MAI by reacting a concentrated aqueous solution of hydroiodic acid with methylamine (40% in methanol) at 0 \\u00b0C for 2 h with constant stirring. Evaporate at 50 \\u00b0C in a rotary evaporator and wash the resulting precipitant three times with ethyl ether and dry in a vacuum at 60 \\u00b0C for 24 h. Equimolar mixtures of the as-synthesised MAI and PbI2 in gamma-butyrolactone were left to stir overnight at 60 \\u00b0C. The MAPbI3 product was obtained by drop-casting the as-prepared solutions on to glass substrates, which were then heated to 100 \\u00b0C and annealed for 30 min. Crystalline MAPbI3 was recovered from the glass after cooling.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A small fragment (approximately 0.1 mm X 0.1 mm X 0.1 mm) was cleaved from one of the solution grown single crystals. Data were collected on a Bruker Smart Apex II three-circle diffractometer at various temperatures between room temperature and 100 K using Mo Ka radiation with a graphite monochromator over the angular range 2.5 to 30.5 \\u00b0 2\\\\theta. Refer to Page 5637 Figure 11.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 456,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            457,\n            458,\n            459\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",\n        \"synthesis_product\": \"Black d6-MAPbI3 Powder\",\n        \"synthesis_description\": \"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \\r\\n\\r\\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \\r\\n\\r\\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 \\u00b0C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",\n        \"experimental_method\": \"Neutron diffraction\",\n        \"experimental_description\": \"Samples were loaded into 8mm diameter vanadium cans in a helium glove- box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Heating and cooling rates were 1K/min. Refer to Page 10 Table 2.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 457,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            456,\n            458,\n            459\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CD3ND2DCl (Sigma-Aldrich, 98 atom % D), DI, D2O, PbI2 (Acros Organics)\",\n        \"synthesis_product\": \"Black d6-MAPbI3 Powder\",\n        \"synthesis_description\": \"Dissolve 1.0 g of CD3ND2DCl in 15 g of 16% DI in D2O (made by dissolving 5 g DI gas in 25 g D2O) and pump to dryness to yield CD3ND2DI. \\r\\n\\r\\nAdd material to 6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \\r\\n\\r\\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 \\u00b0C for 1hr to remove residual solvent. Expect to yield 7.95 g of d6-MAPbI3 (97% yield).\",\n        \"experimental_method\": \"Synchrotron X-ray powder diffraction\",\n        \"experimental_description\": \"The X-ray powder diffraction measurements were performed  on the bending magnet station at DND-CAT sector 5 of the Advanced Photon Source. The X-ray wavelength used was 0.40012(2) \\u00c5, selected to reduce X-ray absorption by the sample to an acceptable level. Temperatures were equilibrated for ~10 min after 1 K changes. Refer to Page 10 Table 2.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 458,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            456,\n            457,\n            459\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CH3ND3I\",\n        \"synthesis_product\": \"Black CH3ND3PbI3 Powder\",\n        \"synthesis_description\": \"Preparation of CH3ND3I: React methylamine gas with HI to yield methyl ammonium iodide. Exchange the two H atoms attached to the nitrogen atoms with D by dissolving the salt in 10 ml D2O (99 atom % D), drying under vacuum, and then repeating two more times. The resulting CH3ND3I was estimated to be better than 98 atom% D on the ammonium group. \\r\\n\\r\\nAdd material to ~6 g of lead iodide and mix in ~25mL of DMF. Upon stirring, obtain pale yellow clear solution. Warm resulting solution and stir overnight in a N2 glove box. \\r\\n\\r\\nEvaporate solution to dryness under vacuum and wash the resulting black solution with dichloromethane and n-propanol. Isolate using suction drying. Anneal solid in nitrogen in the glove box at 140 \\u00b0C for 1hr to remove residual solvent.\",\n        \"experimental_method\": \"Neutron diffraction\",\n        \"experimental_description\": \"Samples were loaded into 8mm diameter vanadium cans in a helium glove-box for analysis on the POWGEN diffractometer situated at the Spallation Neutron Source, Oak Ridge National Laboratory. The analyses of the POWGEN data were carried out using the TOPAS refinement package for Rietveld. Heating and cooling rates were 1K/min. Refer to Page 10 Table 2.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/srep35685\",\n        \"dataset_ID\": 459,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            456,\n            457,\n            458\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures, Phase Transitions and Tricritical Behavior of the Hybrid Perovskite Methyl Ammonium Lead Iodide\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"6\",\n        \"pages_start\": \"35685:1\",\n        \"pages_end\": \"35685:15\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"Black MAPbI3 Powder\",\n        \"synthesis_description\": \"Not explicitly stated in article. But assume close to synthesis methods of the deuterated compounds. Refer to the related data sets.\",\n        \"experimental_method\": \"Synchrotron X-ray powder diffraction\",\n        \"experimental_description\": \"The X-ray powder diffraction measurements were performed  on the bending magnet station at DND-CAT sector 5 of the Advanced Photon Source. The X-ray wavelength used was 0.40012(2) \\u00c5, selected to reduce X-ray absorption by the sample to an acceptable level. Temperatures were equilibrated for ~10 min after 1 K changes. Refer to Page 10 Table 2.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/ncomms11330\",\n        \"dataset_ID\": 460,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            461\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Size-dependent phase transition in methylammonium lead iodide perovskite microplate crystals\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"7:11330\",\n        \"pages_start\": \"1\",\n        \"pages_end\": \"8\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbI2, Si substrate, etc.\",\n        \"synthesis_product\": \"MAPbI3 Thin-film on Si\",\n        \"synthesis_description\": \"Prepare PbI2 aqueous solution (0.1 g per 100 ml) at 80 \\u00b0C and cool to room temperature, which leads to the formation of suspended PbI2 microplates. For the PL measurement samples, dip the Si substrates with 300nm SiO2 (with pre-fabricated markers by photolithography) into the aqueous solution for a few seconds. For the FET samples, define the 5 nm Cr/50nm Au (Pt) electrodes with channel lengths of 8 and 40 mm by photolithography followed by thermal evaporation and lift-off. Grow PbI2 microplates onto the pre-fabricated electrodes by randomly dispersion. Convert the prepared PbI2 microplates into CH3NH3PbI3 by vapour phase intercalation. Refer to source for more details.\",\n        \"experimental_method\": \"Temperature-dependent transport measurement\",\n        \"experimental_description\": \"The thickness of the perovskite microplates was determined by tapping-mode atomic force microscopy (Vecco 5,000 system). TEM images and SAED patterns were acquired in an FEI Titan high-resolution transmission microscopy. \\r\\n\\r\\nTemperature-dependent FET device measurements were carried out in a probe station ((Lakeshore, TTP4) coupled with a precision source/measurement unit (Agilent B2902A). The scanning rate for the transport measurement is 20V/s and the devices were pre-biased at the opposite voltage for 30 s before each measurement.\\r\\n\\r\\nRefer to Page 3; Page 4 figure 2.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Thickness of 30 nm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/ncomms11330\",\n        \"dataset_ID\": 461,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            460\n        ],\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Size-dependent phase transition in methylammonium lead iodide perovskite microplate crystals\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"7:11330\",\n        \"pages_start\": \"1\",\n        \"pages_end\": \"8\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbI2, Si substrate, etc.\",\n        \"synthesis_product\": \"MAPbI3 Thin-film on Si\",\n        \"synthesis_description\": \"Prepare PbI2 aqueous solution (0.1 g per 100 ml) at 80 \\u00b0C and cool to room temperature, which leads to the formation of suspended PbI2 microplates. For the PL measurement samples, dip the Si substrates with 300nm SiO2 (with pre-fabricated markers by photolithography) into the aqueous solution for a few seconds. For the FET samples, define the 5 nm Cr/50nm Au (Pt) electrodes with channel lengths of 8 and 40 mm by photolithography followed by thermal evaporation and lift-off. Grow PbI2 microplates onto the pre-fabricated electrodes by randomly dispersion. Convert the prepared PbI2 microplates into CH3NH3PbI3 by vapour phase intercalation. Refer to source for more details.\",\n        \"experimental_method\": \"Temperature-dependent photoluminescence\",\n        \"experimental_description\": \"The thickness of the perovskite microplates was determined by tapping-mode atomic force microscopy (Vecco 5,000 system). TEM images and SAED patterns were acquired in an FEI Titan high-resolution transmission microscopy. \\r\\n\\r\\nThe PL measurement was conducted under a confocal micro-Raman system (Horiba LABHR) equipped with a 600 g/mm grating in a backscattering configuration excited by an Ar ion laser (488 nm). For the low-temperature measurement, a liquid nitrogen continuous flow cryostat (Cryo Industry of America) was used to control the temperature from 77 to 300 K.\\r\\n\\r\\nKeeping track of the P2/P1 intensity ratio. Increased P2/P1 intensity ratio with decreasing temperature (Fig. 5a and Supplementary Fig. 8).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Thickness < 40nm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.5083792\",\n        \"dataset_ID\": 462,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Temperature-dependent studies of exciton binding energy and phase-transition suppression in (Cs,FA,MA)Pb(I,Br)3 perovskites\",\n        \"journal\": \"APL Materials\",\n        \"vol\": \"7\",\n        \"pages_start\": \"031113-1\",\n        \"pages_end\": \"031113-8\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"MAPbI3 Thin-film on Si\",\n        \"synthesis_description\": \"Not described.\",\n        \"experimental_method\": \"Absorption spectra\",\n        \"experimental_description\": \"Absorption spectra was obtained for 350\\u2013450 nm-thick perovskite thin-films on glass from room temperature down to 5 K. Samples were mounted in a liquid helium bath cryostat and illuminated with a halogen lamp. Absorption spectra were obtained using a 0.275m focal-length monochromator with a 150 lines/mm or 300 lines/mm grating and detected by a charge-coupled device (CCD) camera.\\r\\n\\r\\nA generalized version of the well-known Elliott formula was used to deduce the exciton binding energies and band gaps at successive temperatures.\\r\\n\\r\\nRefer to Fig. 2&3.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jp503337a\",\n        \"dataset_ID\": 463,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Analysis of Multivalley and Multibandgap Absorption and Enhancement of Free Carriers Related to Exciton Screening in Hybrid Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry C\",\n        \"vol\": \"118\",\n        \"pages_start\": \"11566\",\n        \"pages_end\": \"11572\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Refer to experimental from J. Lumin. 1994, 60&61, 269\\u2212274.\",\n        \"experimental_method\": \"Absorption spectra\",\n        \"experimental_description\": \"Experimental data taken from J. Lumin. 1994, 60&61, 269\\u2212274 recorded at 159 K (black line) and 212 K (blue line) and computed spectra for bound and continuum pair states, considering two-particle wave function and effective mass equations for electron and hole (expression 3 with \\u03b3 = 0.03 eV and \\u03bc = 0.16me). Structural phase transition occurs at Tc = 162 K (black dashed line). Refer to Fig. 3 and plots from J. Lumin. 1994, 60&61, 269\\u2212274.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/ncomms4586\",\n        \"dataset_ID\": 464,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition temperature\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Excitons versus free charges in organo-lead tri-halide perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"5\",\n        \"pages_start\": \"3586-1\",\n        \"pages_end\": \"3586-6\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"MAI, PbI2, DMF, Si glass\",\n        \"synthesis_product\": \"MAPbI3 Thin-film on Si\",\n        \"synthesis_description\": \"Dissolve methylammonium iodide and lead (II) iodide (Sigma-Aldrich) in anhydrous N,N-Dimethylformamide (DMF) at a 3:1 molar ratio of MAI to PbI2, with final concentrations of 2.64M methylammonium iodide. The perovskite layer was then formed by spin coating the precursor solutions directly on the glass substrate at 2,000 r.p.m. in air. The flat and thin meso samples were spin coated without dilution but mesoporous samples were spin coated from diluted (three parts in four) precursor solutions. After spin coating, anneal the CH3NH3PbI3 at 150\\u00b0C for 15 min.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Absorption measurements were performed using a spectrophotometer (Perkin Elmer Lambda 1050) and a continuous flow static exchange gas cryostat (Oxford Instruments Optistat CF). The cryostat consist of three chambers, one inside the other. The sample is housed inside the internal chamber filled with gaseous He. The cryogenic liquid (He) is fluxed inside the second chamber allowing temperature control of the He atmosphere of the sample chamber. Eventually, a third chamber is evacuated (~10^-5\\u201310^-6 mbar) in order to assure thermal isolation from the external ambient. Refer to Fig. 1.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 465,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbI2 (99.999% trace metal basis), HI (57 wt. % in H2O, with hypophosphorous acid as stabilizer, assay 99.95%), N,N-Dimethylformamide (anhydrous, 99.8%, Sigma-Aldrich), 2-butanol (99.5%, VWR International)\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"Synthesize AE4T\\u00b7HI in the lab. References [1-3]\\r\\n\\r\\nDissolve 2 mg PbI2 and 3 mg AE4T\\u00b7HI in 0.7 ml DMF with a drop of HI. Then, layer 2 ml 2-butanol on top of the solution (SI Figure S8a). In the experiment, the target crystals came out after several days (Figure S8b).\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker D8 ADVANCE Series II at room temperature.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry (SI Section X)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic000794i\",\n        \"dataset_ID\": 466,\n        \"id\": 53,\n        \"compound_name\": \"5,5\\u2018 \\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018 \\u2018:5\\u2018 \\u2018,2\\u2018 \\u2018\\u2018-quaterthiophene antimony iodide\",\n        \"formula\": \"C20H22N2S4Sb(2/3)I4\",\n        \"group\": \"5,5\\u2018 \\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018 \\u2018:5\\u2018 \\u2018,2\\u2018 \\u2018\\u2018-quaterthiophene tetraiodoantimonate(II), AE4TSb(2/3)I4, (AEQT)Sb(2/3)I4, AEQTSb(2/3)I4, (H2AEQT)Sb(2/3)I4, C20H22S4N2Sb(2/3)I4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"Sb(2/3)I4, Antimony iodide\",\n        \"iupac\": \"5,5\\u2018 \\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018 \\u2018:5\\u2018 \\u2018,2\\u2018 \\u2018\\u2018-quaterthiophene antimony(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-Inorganic Perovskites Containing Trivalent Metal Halide Layers: The Templating Influence of the Organic Cation Layer\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"39\",\n        \"pages_start\": \"6107\",\n        \"pages_end\": \"6113\",\n        \"year\": \"2000\",\n        \"synthesis_starting_materials\": \"AEQT2HI (161.4 mg; 0.24 mmol), SbI3 salts (Aldrich, 99.999%, anhydrous), ethylene glycol (Aldrich, anhydrous, 99.8%), concentrated (57 wt %) aqueous HI (Aldrich, stabilized, 99.99%), 2-butanol (Aldrich, anhydrous, 99.5%)\",\n        \"synthesis_product\": \"Dark red, sheetlike crystals\",\n        \"synthesis_description\": \"Synthesize AEQT2HI from method described in [1].\\r\\n\\r\\nPurify the SbI3 salts (Aldrich, 99.999%, anhydrous) by sublimation. \\r\\n\\r\\nWeigh equimolar quantities of AEQT2HI (161.4 mg; 0.24 mmol) and SbI3 and add to a test tube under an inert atmosphere. Dissolve the contents at 112 \\u00b0C in a solvent mixture of 36 mL of ethylene glycol and 0.6 mL of concentrated aqueous HI. Gradually add 18 mL of 2-butanol to form a small amount of red precipitate. Heat the mixture to 116 \\u00b0C in a sealed tube to dissolve the mixture into a solution. Slow cool the solution at 1.5 \\u00b0C/h to -20 \\u00b0C to produce of dark red, sheetlike crystals of the (H2AEQT)Sb(2/3)I4 compound.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A very thin, sheetlike crystal, with the approximate dimensions \\u00180.005 mm \\u0002X 0.12 mm X\\u0002 0.27 mm [<0.01 mm X\\u0002 0.06 mm \\u0002X 0.24 mm] was selected. Collect a full sphere of data at room temperature using a Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo-Ka radiation) 0.71073 \\u00c5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2/m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic000794i\",\n        \"dataset_ID\": 467,\n        \"id\": 54,\n        \"compound_name\": \"5,5\\u2018 \\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018 \\u2018:5\\u2018 \\u2018,2\\u2018 \\u2018\\u2018-quaterthiophene bismuth iodide\",\n        \"formula\": \"C20H22N2S4Bi(2/3)I4\",\n        \"group\": \"5,5\\u2018 \\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018 \\u2018:5\\u2018 \\u2018,2\\u2018 \\u2018\\u2018-quaterthiophene tetraiodobismate(II), AE4TBi(2/3)I4, (AEQT)Bi(2/3)I4, AEQTBi(2/3)I4, (H2AEQT)Bi(2/3)I4, C20H22S4N2Bi(2/3)I4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"Bi(2/3)I4, Bismuth iodide\",\n        \"iupac\": \"5,5\\u2018 \\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018 \\u2018:5\\u2018 \\u2018,2\\u2018 \\u2018\\u2018-quaterthiophene bismuth(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-Inorganic Perovskites Containing Trivalent Metal Halide Layers: The Templating Influence of the Organic Cation Layer\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"39\",\n        \"pages_start\": \"6107\",\n        \"pages_end\": \"6113\",\n        \"year\": \"2000\",\n        \"synthesis_starting_materials\": \"AEQT2HI (161.4 mg; 0.24 mmol), BiI3 salts (Aldrich, 99.999%, anhydrous), ethylene glycol (Aldrich, anhydrous, 99.8%), concentrated (57 wt %) aqueous HI (Aldrich, stabilized, 99.99%), 2-butanol (Aldrich, anhydrous, 99.5%)\",\n        \"synthesis_product\": \"Dark red, sheetlike crystals\",\n        \"synthesis_description\": \"Synthesize AEQT2HI from method described in [1].\\r\\n\\r\\nPurify the BiI3 salts (Aldrich, 99.999%, anhydrous) by sublimation. \\r\\n\\r\\nWeigh equimolar quantities of AEQT2HI (161.4 mg; 0.24 mmol) and BiI3 and add to a test tube under an inert atmosphere. Dissolve the contents at 112 \\u00b0C in a solvent mixture of 36 mL of ethylene glycol and 0.6 mL of concentrated aqueous HI. Gradually add 18 mL of 2-butanol to form a small amount of red precipitate. Heat the mixture to 116 \\u00b0C in a sealed tube to dissolve the mixture into a solution. Slow cool the solution at 1.5 \\u00b0C/h to -20 \\u00b0C to produce dark red, sheetlike crystals of the (H2AEQT)Bi(2/3)I4 compound.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A very thin, sheetlike crystal, with the approximate dimensions \\u00180.005 mm \\u0002X 0.12 mm X\\u0002 0.27 mm [<0.01 mm X\\u0002 0.06 mm \\u0002X 0.24 mm] was selected. Collect a full sphere of data at room temperature using a Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo-Ka radiation) 0.71073 \\u00c5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2/m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b06143\",\n        \"dataset_ID\": 469,\n        \"id\": 56,\n        \"compound_name\": \"Tetra(ethylammonium) lead bromide\",\n        \"formula\": \"C8H32N4Pb3Br10\",\n        \"group\": \"tetra(ethanaminium) decabromo triplumbate(II), EA4Pb3Br10, (CH3CH2NH3)4Pb3Br10, (C2H8N)4Pb3Br10\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"Pb3Br10, Lead bromide\",\n        \"iupac\": \"tetra(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable White-Light Emission in Single-Cation-Templated Three-Layered 2D Perovskites (CH3CH2NH3)4Pb3Br10\\u2212xClx\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"11956\",\n        \"pages_end\": \"11963\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), PbBr2 (98%), ethylamine hydrochloride (98%), and hydrobromic acid ( 48%)\",\n        \"synthesis_product\": \"Yellow rectangular plate-like crystals of (CH3CH2NH3)4Pb3Br10 [Yield: 53.3% w.r.t. Pb]\",\n        \"synthesis_description\": \"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 10 mL of 48% hydrobromic acid at 180 \\u00b0C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"Spectra were collected using a Shimadzu UV-3600 UV\\u2212vis\\u2212 NIR spectrometer operating in the 200\\u22121000 nm region using BaSO4 as the reference of 100% reflectance. The reflectance was converted to absorption according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aba2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b06143\",\n        \"dataset_ID\": 470,\n        \"id\": 56,\n        \"compound_name\": \"Tetra(ethylammonium) lead bromide\",\n        \"formula\": \"C8H32N4Pb3Br10\",\n        \"group\": \"tetra(ethanaminium) decabromo triplumbate(II), EA4Pb3Br10, (CH3CH2NH3)4Pb3Br10, (C2H8N)4Pb3Br10\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"Pb3Br10, Lead bromide\",\n        \"iupac\": \"tetra(ethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable White-Light Emission in Single-Cation-Templated Three-Layered 2D Perovskites (CH3CH2NH3)4Pb3Br10\\u2212xClx\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"11956\",\n        \"pages_end\": \"11963\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), PbBr2 (98%), ethylamine hydrochloride (98%), and hydrobromic acid ( 48%)\",\n        \"synthesis_product\": \"Yellow rectangular plate-like crystals of (CH3CH2NH3)4Pb3Br10 [Yield: 53.3% w.r.t. Pb]\",\n        \"synthesis_description\": \"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 10 mL of 48% hydrobromic acid at 180 \\u00b0C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an STOE IPDS 2 or IPDS 2T diffractometer with graphite monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2. Integration and numerical absorption corrections were done using the STOE X-AREA programs.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aba2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b06143\",\n        \"dataset_ID\": 472,\n        \"id\": 55,\n        \"compound_name\": \"Tetra(ethylammonium) lead chloride\",\n        \"formula\": \"C8H32N4Pb3Cl10\",\n        \"group\": \"tetra(ethanaminium) decachloro triplumbate(II), EA4Pb3Cl10, (CH3CH2NH3)4Pb3Cl10, (C2H8N)4Pb3Cl10\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"Pb3Cl10, Lead chloride\",\n        \"iupac\": \"tetra(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable White-Light Emission in Single-Cation-Templated Three-Layered 2D Perovskites (CH3CH2NH3)4Pb3Br10\\u2212xClx\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"11956\",\n        \"pages_end\": \"11963\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), PbCl2 (98%), ethylamine hydrochloride (98%), hydrochloric acid (ACS reagent, 37%)\",\n        \"synthesis_product\": \"Transparent rectangular plate-like crystals of (CH3CH2NH3)4Pb3Cl10 [Yield: 53.3% w.r.t. Pb]\",\n        \"synthesis_description\": \"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 20 mL of 37% hydrochloric acid at 180 \\u00b0C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating until about 70% of the above solution was evaporated. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"Spectra were collected using a Shimadzu UV-3600 UV\\u2212vis\\u2212 NIR spectrometer operating in the 200\\u22121000 nm region using BaSO4 as the reference of 100% reflectance. The reflectance was converted to absorption according to the Kubelka\\u2212Munk equation: \\u03b1/S =(1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b06143\",\n        \"dataset_ID\": 473,\n        \"id\": 55,\n        \"compound_name\": \"Tetra(ethylammonium) lead chloride\",\n        \"formula\": \"C8H32N4Pb3Cl10\",\n        \"group\": \"tetra(ethanaminium) decachloro triplumbate(II), EA4Pb3Cl10, (CH3CH2NH3)4Pb3Cl10, (C2H8N)4Pb3Cl10\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"Pb3Cl10, Lead chloride\",\n        \"iupac\": \"tetra(ethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable White-Light Emission in Single-Cation-Templated Three-Layered 2D Perovskites (CH3CH2NH3)4Pb3Br10\\u2212xClx\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"11956\",\n        \"pages_end\": \"11963\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), PbCl2 (98%), ethylamine hydrochloride (98%), hydrochloric acid (ACS reagent, 37%)\",\n        \"synthesis_product\": \"Transparent rectangular plate-like crystals of (CH3CH2NH3)4Pb3Cl10 [Yield: 53.3% w.r.t. Pb]\",\n        \"synthesis_description\": \"Under stirring, 1.338 g (6 mmol) of 99.9% PbO powder was dissolved in 20 mL of 37% hydrochloric acid at 180 \\u00b0C until the solution turned colorless. Then, 0.652 g (8 mmol) of ethylamine hydrochloride was added directly to the above solution under heating until about 70% of the above solution was evaporated. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an STOE IPDS 2 or IPDS 2T diffractometer with graphite monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2. Integration and numerical absorption corrections were done using the STOE X-AREA programs.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 474,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation was used to collect the single crystal XRD data.\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 475,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation was used to collect the single crystal XRD data.\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 476,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation was used to collect the single crystal XRD data.\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/n\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 477,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1976\n        ],\n        \"primary_name\": \"PL excitation peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 478,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1980\n        ],\n        \"primary_name\": \"PL excitation peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 479,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1985\n        ],\n        \"primary_name\": \"PL excitation peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/n\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 480,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1975,\n            1977\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 481,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1978,\n            1979\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether.In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 482,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1986,\n            1987\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 483,\n        \"id\": 60,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"C12H32N2PbI4\",\n        \"group\": \"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"hexylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HI, HA (C6H13NH3), Et2O, PbI2\",\n        \"synthesis_product\": \"Powder of (C6H13NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). To prepare powder for XRD, drop-cast thin film from 200 mg/mL solutions and anneal at 70 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Bruker X-ray D8 Advance diffractometer with Cu K\\u03b11,2 radiation (\\u03bb = 1.541 \\u00c5). Spectra were collected with an angular range of 5 < 2\\u03b8 < 60\\u00b0 and step size of 0.01022 \\u00b0 over 60 minutes. Rietveld analysis was carried out using the TOPAS program. Low-temperature measurements were made on cooling between 300\\u221212K using an Oxford Cyrosytem PheniX stage.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 484,\n        \"id\": 61,\n        \"compound_name\": \"Bis(dodecylammonium) lead iodide\",\n        \"formula\": \"C24H56N2PbI4\",\n        \"group\": \"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",\n        \"organic\": \"C12H28N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(dodecyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"dodecylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HI, DA (C12H25NH3), Et2O, PbI2\",\n        \"synthesis_product\": \"Powder of (C12H25NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). To prepare powder for XRD, drop-cast thin film from 200 mg/mL solutions and anneal at 70 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Bruker X-ray D8 Advance diffractometer with Cu K\\u03b11,2 radiation (\\u03bb = 1.541 \\u00c5). Spectra were collected with an angular range of 5 < 2\\u03b8 < 60\\u00b0 and step size of 0.01022\\u00b0 over 60 minutes. Rietveld analysis was carried out using the TOPAS program. Low-temperature\\r\\nmeasurements were made on cooling between 300\\u221212K using an Oxford Cyrosytem PheniX stage.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 485,\n        \"id\": 61,\n        \"compound_name\": \"Bis(dodecylammonium) lead iodide\",\n        \"formula\": \"C24H56N2PbI4\",\n        \"group\": \"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",\n        \"organic\": \"C12H28N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(dodecyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"dodecylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HI, DA (C12H25NH3), Et2O, PbI2\",\n        \"synthesis_product\": \"Thin film of (C12H25NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence spectra\",\n        \"experimental_description\": \"Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 486,\n        \"id\": 60,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"C12H32N2PbI4\",\n        \"group\": \"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"hexylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HI, HA (C6H13NH3), Et2O, PbI2\",\n        \"synthesis_product\": \"Thin film of (C6H13NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence spectra\",\n        \"experimental_description\": \"Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 488,\n        \"id\": 63,\n        \"compound_name\": \"2-methyl-1,5-pentanediamine lead bromide\",\n        \"formula\": \"C6H18N2PbBr4\",\n        \"group\": \"methyl-2-pentane-1,5-diaminium tetrabromoplumbate(II), (MPenDA)PbBr4, NH3C5H9CH3NH3PbBr4\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"methyl-2-pentane-1,5-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"2-methyl-1,5-pentanediamine, PbBr2,  HBr\",\n        \"synthesis_product\": \"needle-like colorless crystal\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.35 mmol 2-methyl-1,5-pentanediamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C 2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 489,\n        \"id\": 64,\n        \"compound_name\": \"Bis(butylammonium) lead bromide\",\n        \"formula\": \"C8H24N2PbBr4\",\n        \"group\": \"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(butyl-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"n-butylamine, PbBr2, HBr\",\n        \"synthesis_product\": \"plate-like colorless crystals\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.7 mmol n-butylamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 490,\n        \"id\": 65,\n        \"compound_name\": \"1,8-octyldiammonium lead bromide\",\n        \"formula\": \"C8H22N2PbBr4\",\n        \"group\": \"octane-1,8-diaminium tetrabromoplumbate(II), (ODA)PbBr4, NH3C8H16NH3PbBr4\",\n        \"organic\": \"C8H22N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"octane-1,8-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"octanediamine, PbBr2, HBr\",\n        \"synthesis_product\": \"plate-like colorless crystals\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.35 mmol octanediamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 491,\n        \"id\": 66,\n        \"compound_name\": \"bis(4-aminobutonic acid) lead bromide\",\n        \"formula\": \"C8H20N2O4PbBr4\",\n        \"group\": \"bis(4-aminobutanoic acid) tetrabromoplumbate(II), (GABA)2PbBr4, C8H20O4N2PbBr4, (C4H10NO2)2PbBr4\",\n        \"organic\": \"C4H10NO2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(4-aminobutanoic acid) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"3-carboxypropan-1-amine, PbBr2, HBr\",\n        \"synthesis_product\": \"plate-like colorless crystals\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.7 mmol 3-carboxypropan-1-amine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 492,\n        \"id\": 67,\n        \"compound_name\": \"3-(2-ammonioethyl)anilinium lead bromide\",\n        \"formula\": \"C8H14N2PbBr4\",\n        \"group\": \"3-(2-ethanaminium)anilinium tetrabromoplumbate(II), (AEA)PbBr4\",\n        \"organic\": \"C8H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-(2-ethanaminium)anilinium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"3-(2-ammonioethyl)anilin, PbBr2, HBr\",\n        \"synthesis_product\": \"plate-like colorless crystals\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.35 mmol 3-(2-ammonioethyl)anilin are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D85 diffractometer at the Advanced Light Source beamline 11.3.1 (\\u03bb=0.7749 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 493,\n        \"id\": 68,\n        \"compound_name\": \"1,4-butyldiammonium lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"butyl-1,4-diaminium tetrabromoplumbate(II), (BDA)PbBr4, C4N2H14PbBr4, NH3C4H8NH3PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"butyl-1,4-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"butanediamine, PbBr2, HBr\",\n        \"synthesis_product\": \"plate-like colorless crystals\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.35 mmol butanediamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 494,\n        \"id\": 69,\n        \"compound_name\": \"Histammonium lead bromide\",\n        \"formula\": \"C5H11N3PbBr4\",\n        \"group\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Histamine, PbBr2, HBr\",\n        \"synthesis_product\": \"plate-like yellow crystals\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.35 mmol histamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5).\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7sc01590a\",\n        \"dataset_ID\": 495,\n        \"id\": 69,\n        \"compound_name\": \"Histammonium lead bromide\",\n        \"formula\": \"C5H11N3PbBr4\",\n        \"group\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural origins of broadband emission from layered Pb\\u2013Br hybrid perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"4497\",\n        \"pages_end\": \"4504\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Histamine, PbBr2, HBr\",\n        \"synthesis_product\": \"plate-like yellow crystals\",\n        \"synthesis_description\": \"0.34 mmol PbBr2, 0.35 mmol histamine are mixed in 3 mL of 9M HBr. The mixture is then heated to 100 \\u02daC for 2 h to dissolve the solid, and then slowly cooled down to room temperature at \\u22122 \\u00b0C\\u00b7hr\\u22121.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector employing Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5).\",\n        \"physical_property\": \"296.15\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 496,\n        \"id\": 70,\n        \"compound_name\": \"Tris(2,6-dimethylpiperazine) lead bromide\",\n        \"formula\": \"C18H48N6Pb2Br10\",\n        \"group\": \"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2Br10, Lead bromide\",\n        \"iupac\": \"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 2,6-dimethylpiperazine (97%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 2,6-dimethylpiperazine (342 mg, 3 mmol). Add the protonated 2,6-dimethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using a Bruker DUO or Molly instrument with a Mo K\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) with MX Optics at 250 K. Post-processing using APEX3 software and OLEX2 program package.\",\n        \"physical_property\": \"\\u2248250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 497,\n        \"id\": 71,\n        \"compound_name\": \"4-(aminomethyl)piperidine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperidine lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 4-(aminomethyl)piperidine (96%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 3 mmol of 4-(aminomethyl)piperidine. Add the protonated 4-(aminomethyl)-piperidine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pca2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 498,\n        \"id\": 72,\n        \"compound_name\": \"1-ethylpiperazine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-ethane-1,3-diazinanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 1-ethylpiperazine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 1-ethylpiperazine (342 mg, 3 mmol). Add the protonated 1-ethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 499,\n        \"id\": 73,\n        \"compound_name\": \"Bis(1-methylpiperazine) lead bromide\",\n        \"formula\": \"C10H28N4Pb3Br10\",\n        \"group\": \"bis(1-methane-1,3-diazinanium) decabromo triplumbate(II), (mpz)2Pb3Br10, (C5H14N2)2Pb3Br10\",\n        \"organic\": \"C5H14N2\",\n        \"inorganic\": \"Pb3Br10, Lead bromide\",\n        \"iupac\": \"bis(1-methane-1,3-diazinanium) lead (II) bromide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 1-methylpiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 1-methylpiperazine (200 mg, 2 mmol). Add the protonated 1-methylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 500,\n        \"id\": 74,\n        \"compound_name\": \"Homopiperazine lead bromide\",\n        \"formula\": \"C5H14N2PbBr4\",\n        \"group\": \"1,4-diazepanium tetrabromoplumbate(II), (hmp)PbBr4, (C5H14N2)PbBr4\",\n        \"organic\": \"C5H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1,4-diazepanium lead bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), homopiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of homopiperazine (300 mg, 3 mmol). Add the protonated homopiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 501,\n        \"id\": 75,\n        \"compound_name\": \"Hexamethylenimine lead bromide\",\n        \"formula\": \"C6H14NPbBr3\",\n        \"group\": \"Hexamethylenimine tribromoplumbate(II), (hex)PbBr3, (C6H14N)PbBr3\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azepanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), hexamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of hexamethylenimine (297 mg, 3 mmol). Add the protonated hexamethylenimine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using either Bruker DUO or Molly instrument with a Mo K\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) with MX Optics at 250 K. Post-processing using APEX3 software and OLEX2 program package.\",\n        \"physical_property\": \"\\u2248250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 502,\n        \"id\": 76,\n        \"compound_name\": \"Heptamethylenimine lead bromide\",\n        \"formula\": \"C7H16NPbBr3\",\n        \"group\": \"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",\n        \"organic\": \"C7H16N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azocanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), heptamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of heptamethylenimine (339 mg, 3 mmol). Add the protonated heptamethylenimine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using either an STOE IPDS 2 or IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2 at 293 K. Post-processing using STOE X-AREA programs.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 503,\n        \"id\": 70,\n        \"compound_name\": \"Tris(2,6-dimethylpiperazine) lead bromide\",\n        \"formula\": \"C18H48N6Pb2Br10\",\n        \"group\": \"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2Br10, Lead bromide\",\n        \"iupac\": \"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 2,6-dimethylpiperazine (97%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 2,6-dimethylpiperazine (342 mg, 3 mmol). Add the protonated 2,6-dimethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV\\u2212vis\\u2212NIR spectrometer operating in the 200\\u22121000 nm region. Convert reflectance to absorption according to the Kubelka\\u2212Munk equation to estimate the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 504,\n        \"id\": 71,\n        \"compound_name\": \"4-(aminomethyl)piperidine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperidine lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 4-(aminomethyl)piperidine (96%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 3 mmol of 4-(aminomethyl)piperidine. Add the protonated 4-(aminomethyl)-piperidine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV\\u2212vis\\u2212NIR spectrometer operating in the 200\\u22121000 nm region. Convert reflectance to absorption according to the Kubelka\\u2212Munk equation to estimate the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pca2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 505,\n        \"id\": 72,\n        \"compound_name\": \"1-ethylpiperazine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-ethane-1,3-diazinanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 1-ethylpiperazine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 1-ethylpiperazine (342 mg, 3 mmol). Add the protonated 1-ethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV\\u2212vis\\u2212NIR spectrometer operating in the 200\\u22121000 nm region. Convert reflectance to absorption according to the Kubelka\\u2212Munk equation to estimate the band gap.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 506,\n        \"id\": 73,\n        \"compound_name\": \"Bis(1-methylpiperazine) lead bromide\",\n        \"formula\": \"C10H28N4Pb3Br10\",\n        \"group\": \"bis(1-methane-1,3-diazinanium) decabromo triplumbate(II), (mpz)2Pb3Br10, (C5H14N2)2Pb3Br10\",\n        \"organic\": \"C5H14N2\",\n        \"inorganic\": \"Pb3Br10, Lead bromide\",\n        \"iupac\": \"bis(1-methane-1,3-diazinanium) lead (II) bromide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 1-methylpiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 1-methylpiperazine (200 mg, 2 mmol). Add the protonated 1-methylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV\\u2212vis\\u2212NIR spectrometer operating in the 200\\u22121000 nm region. Convert reflectance to absorption according to the Kubelka\\u2212Munk equation to estimate the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 507,\n        \"id\": 74,\n        \"compound_name\": \"Homopiperazine lead bromide\",\n        \"formula\": \"C5H14N2PbBr4\",\n        \"group\": \"1,4-diazepanium tetrabromoplumbate(II), (hmp)PbBr4, (C5H14N2)PbBr4\",\n        \"organic\": \"C5H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1,4-diazepanium lead bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), homopiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of homopiperazine (300 mg, 3 mmol). Add the protonated homopiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV\\u2212vis\\u2212NIR spectrometer operating in the 200\\u22121000 nm region. Convert reflectance to absorption according to the Kubelka\\u2212Munk equation to estimate the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 508,\n        \"id\": 75,\n        \"compound_name\": \"Hexamethylenimine lead bromide\",\n        \"formula\": \"C6H14NPbBr3\",\n        \"group\": \"Hexamethylenimine tribromoplumbate(II), (hex)PbBr3, (C6H14N)PbBr3\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azepanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), hexamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of hexamethylenimine (297 mg, 3 mmol). Add the protonated hexamethylenimine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV\\u2212vis\\u2212NIR spectrometer operating in the 200\\u22121000 nm region. Convert reflectance to absorption according to the Kubelka\\u2212Munk equation to estimate the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 509,\n        \"id\": 76,\n        \"compound_name\": \"Heptamethylenimine lead bromide\",\n        \"formula\": \"C7H16NPbBr3\",\n        \"group\": \"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",\n        \"organic\": \"C7H16N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azocanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), heptamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of heptamethylenimine (339 mg, 3 mmol). Add the protonated heptamethylenimine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"First, perform optical diffuse reflectance using a Shimadzu UV-3600 UV\\u2212vis\\u2212NIR spectrometer operating in the 200\\u22121000 nm region. Convert reflectance to absorption according to the Kubelka\\u2212Munk equation to estimate the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 510,\n        \"id\": 70,\n        \"compound_name\": \"Tris(2,6-dimethylpiperazine) lead bromide\",\n        \"formula\": \"C18H48N6Pb2Br10\",\n        \"group\": \"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2Br10, Lead bromide\",\n        \"iupac\": \"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 2,6-dimethylpiperazine (97%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 2,6-dimethylpiperazine (342 mg, 3 mmol). Add the protonated 2,6-dimethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 511,\n        \"id\": 71,\n        \"compound_name\": \"4-(aminomethyl)piperidine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperidine lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 4-(aminomethyl)piperidine (96%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 3 mmol of 4-(aminomethyl)piperidine. Add the protonated 4-(aminomethyl)-piperidine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pca2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 512,\n        \"id\": 72,\n        \"compound_name\": \"1-ethylpiperazine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-ethane-1,3-diazinanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 1-ethylpiperazine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 1-ethylpiperazine (342 mg, 3 mmol). Add the protonated 1-ethylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 513,\n        \"id\": 73,\n        \"compound_name\": \"Bis(1-methylpiperazine) lead bromide\",\n        \"formula\": \"C10H28N4Pb3Br10\",\n        \"group\": \"bis(1-methane-1,3-diazinanium) decabromo triplumbate(II), (mpz)2Pb3Br10, (C5H14N2)2Pb3Br10\",\n        \"organic\": \"C5H14N2\",\n        \"inorganic\": \"Pb3Br10, Lead bromide\",\n        \"iupac\": \"bis(1-methane-1,3-diazinanium) lead (II) bromide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), 1-methylpiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of 1-methylpiperazine (200 mg, 2 mmol). Add the protonated 1-methylpiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 514,\n        \"id\": 74,\n        \"compound_name\": \"Homopiperazine lead bromide\",\n        \"formula\": \"C5H14N2PbBr4\",\n        \"group\": \"1,4-diazepanium tetrabromoplumbate(II), (hmp)PbBr4, (C5H14N2)PbBr4\",\n        \"organic\": \"C5H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1,4-diazepanium lead bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), homopiperazine (99%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of homopiperazine (300 mg, 3 mmol). Add the protonated homopiperazine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 515,\n        \"id\": 75,\n        \"compound_name\": \"Hexamethylenimine lead bromide\",\n        \"formula\": \"C6H14NPbBr3\",\n        \"group\": \"Hexamethylenimine tribromoplumbate(II), (hex)PbBr3, (C6H14N)PbBr3\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azepanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), hexamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of hexamethylenimine (297 mg, 3 mmol). Add the protonated hexamethylenimine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 516,\n        \"id\": 76,\n        \"compound_name\": \"Heptamethylenimine lead bromide\",\n        \"formula\": \"C7H16NPbBr3\",\n        \"group\": \"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",\n        \"organic\": \"C7H16N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azocanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2(98%), heptamethylenimine (98%), hydrobromic acid (ACS reagent, 48%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Dissolve 1.10 g (3 mmol) of PbBr2 in 4 mL of HBr under heating and stirring at 122 \\u00b0C (A). Add 1 mL of HBr into a separate vial of heptamethylenimine (339 mg, 3 mmol). Add the protonated heptamethylenimine solution into A under heating for 2 min and cool to room temperature.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"Excite with 330 nm photons produced from an optical parametric amplifier, which is pumped by a Ti:sapphire amplifier with 800 nm output at 2 kHz repetition rate. Time-integrated photoluminescence spectra were captured with a CCD camera; time-resolved PL spectra were captured with a streak camera.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/acsmaterialslett.9b00102\",\n        \"dataset_ID\": 520,\n        \"id\": 84,\n        \"compound_name\": \"Phenethylammonium perfluorophenethylammonium lead iodide\",\n        \"formula\": \"C32H38N4F2Pb2I8\",\n        \"group\": \"phenethanaminium perfluorophenethanaminium octaiodo diplumbate(II)), ((PEA)0.5(F[5]-PEA)0.5)2PbI4\",\n        \"organic\": \"C8H12N, F5C8H7N\",\n        \"inorganic\": \"Pb2I8, Lead iodide\",\n        \"iupac\": \"phenethanaminium perfluorophenethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Aryl-Perfluoroaryl Interaction in TwoDimensional Organic\\u2212Inorganic Hybrid Perovskites Boosts Stability and Photovoltaic Efficiency\",\n        \"journal\": \"ACS Materials Letters\",\n        \"vol\": \"1\",\n        \"pages_start\": \"171\",\n        \"pages_end\": \"176\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"n-Butanol, 57wt% stabilized HI (Alfa Aesar), perfluorophenethylammonium iodide (F5-PEAI; synthesized), phenethylammonium iodide (PEAI; synthesized)\",\n        \"synthesis_product\": \"Yellow plate-like crystals\",\n        \"synthesis_description\": \"In 0.5 ml n-Butanol and 0.1 ml 57wt% stabilized HI, 69.2 mg PbI2, 50.9 mg F5-PEAI and 37.4 mg PEAI were dissolved at 95 \\u00b0C. The solution was slowly cooled down at 1 \\u00b0C/h to room temperature and the solids were collected.\",\n        \"experimental_method\": \"Single crystal X-ray Diffraction\",\n        \"experimental_description\": \"Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo K radiation source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\",\n        \"physical_property\": \"302.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/acsmaterialslett.9b00102\",\n        \"dataset_ID\": 521,\n        \"id\": 85,\n        \"compound_name\": \"Bis(perfluorophenethylammonium) lead iodide\",\n        \"formula\": \"C32H38F2N4Pb2I8\",\n        \"group\": \"bis(2-(perfluorophenyl)ethan-1-aminium) octoiodo diplumbate(II), (F[5]-PEA)2PbI4\",\n        \"organic\": \"C8H7F5N\",\n        \"inorganic\": \"Pb2I8, Lead iodide\",\n        \"iupac\": \"bis(2-(perfluorophenyl)ethan-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Aryl-Perfluoroaryl Interaction in TwoDimensional Organic\\u2212Inorganic Hybrid Perovskites Boosts Stability and Photovoltaic Efficiency\",\n        \"journal\": \"ACS Materials Letters\",\n        \"vol\": \"1\",\n        \"pages_start\": \"171\",\n        \"pages_end\": \"176\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"n-Butanol, 57wt% stabilized HI (Alfa Aesar), perfluorophenethylammonium iodide (F5-PEAI; synthesized)\",\n        \"synthesis_product\": \"Yellow plate-like crystals\",\n        \"synthesis_description\": \"In 0.5 ml n-Butanol and 0.1 ml 57wt% stabilized HI, 69.2 mg PbI2 and 101.7 mg F5-PEAI were dissolved  at 95 \\u00b0C. The solution was slowly cooled down at 1 \\u00b0C/h to room temperature and the solids were collected.\",\n        \"experimental_method\": \"Single crystal X-ray Diffraction\",\n        \"experimental_description\": \"Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo K radiation source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aba2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 522,\n        \"id\": 89,\n        \"compound_name\": \"AzoEA2PbI4\",\n        \"formula\": \"C28H32N6PbI4\",\n        \"group\": \"AzoEA2 tetraiodoplumbate(II), AzoEA2PbI4\",\n        \"organic\": \"C28H32N6\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"UV-induced Exfoliation of Two-Dimensional Organic-Inorganic Hy-brid Perovskite with Azobenzene based Organic Cations\",\n        \"journal\": \"Unpublished\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"PbI2, AzoEAI\",\n        \"synthesis_product\": \"AzoEA2PbI4\",\n        \"synthesis_description\": \"stoichiometric ratio of AzoEA2PbI4 and PbI2 were dissolved in CH3CN at 90\\u00b0C and cooled down to room temperature at 1\\u00b0C/h. The solids were collected\",\n        \"experimental_method\": \"The single crystal data was collected by Agilent Gemini E diffractometer \\uff08Mo\\uff0c50kV 40mA\\uff09at 173 K.\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"DOI: 10.1002/anie.201702825\",\n        \"dataset_ID\": 525,\n        \"id\": 90,\n        \"compound_name\": \"N,N\\u2032-dimethylethylene diaminium tin bromide\",\n        \"formula\": \"C4H14N2SnBr4\",\n        \"group\": \"N,N\\u201a\\u00c4\\u2264-dimethylethylene diaminium tetrabromostannate(II), C4N2H14SnBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"N,N\\u2032-dimethylethylene diaminium tin (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Low-Dimensional Organic Tin Bromide Perovskites and Their Photoinduced Structural Transformation\",\n        \"journal\": \"Angew. Chem. Int. Ed.\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9018\",\n        \"pages_end\": \"9022\",\n        \"year\": \"17\",\n        \"synthesis_starting_materials\": \"Tin(II) bromide (SnBr2), hydrobromic acid (HBr, 48 wt. % in H2O), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), N, N\\u2019-dimethylethylenediamine (99 %)\",\n        \"synthesis_product\": \"colorless needle-like C4N2H14SnBr4 crystals\",\n        \"synthesis_description\": \"0.5 mmol Tin(II) bromide was dissolved in 3 ml HBr and 1 ml H3PO2. Under N2, the solution was heated up to 120 \\u00b0C with constant magnetic stirring. 0.5 mmol N, N\\u2019-dimethylethylenediamine was injected into the hot solution and then the solution was cooled down to room temperature. The solids were collected.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation (= 0.71073 \\u00c5) was used for single crystal diffraction at 100 K.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"I 2/m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01312\",\n        \"dataset_ID\": 526,\n        \"id\": 86,\n        \"compound_name\": \"2-dimethylamino-1-ethylamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N,N,N-dimethylethanaminium tetrabromoplumbate(II), (DMEN)PbBr4,2-(dimethylamino)ethylamine, ((CH3)2NH(CH2)2NH3)PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N,N,N-dimethylethanaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\\u03b1-(DMEN)PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"White-Light Emission and Structural Distortion in New Corrugated Two-Dimensional Lead Bromide Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5210\",\n        \"pages_end\": \"5215\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 2-(dimethylamino)ethylamine\",\n        \"synthesis_product\": \"colorless rhombic shaped crystals\",\n        \"synthesis_description\": \"0.669g PbO powder was added into 6.0 ml HBr and 1.0 mL of H3PO2 under stirring while heating at 150 \\u00b0C until PbO was dissolved. 0.264g 2-(dimethylamino)ethylamine was added to the above solution under heating and stirring.\\r\\nAfter cooling and leaving the solution for 10-14 days, \\u03b1-(DMEN)PbBr4 crystals were obtained.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\\r\\nIntegration and correction of the data were done by STOE X-AREA programs. Crystal structures were resolved by using OLEX2 program package by full-matrix least-squares on F^2.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b01025\",\n        \"dataset_ID\": 527,\n        \"id\": 479,\n        \"compound_name\": \"Methylammonium Germanium Iodide\",\n        \"formula\": \"CH3NH3GeI3\",\n        \"group\": \"MAGeI3, methylammonium triiodogermaniate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"GeI3, Germanium iodide\",\n        \"iupac\": \"methanaminium germanium iodide\",\n        \"last_update\": \"2022-05-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Germanium Iodide Perovskite Semiconductors: Active Lone Pairs, Structural Distortions, Direct and Indirect Energy Gaps, and Strong Nonlinear Optical Properties\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"137\",\n        \"pages_start\": \"6804\",\n        \"pages_end\": \"6819\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), methylamine (CH3NH2)\",\n        \"synthesis_product\": \"deep red, elongated hexagonal plate-like CH3NH3GeI3 crystals\",\n        \"synthesis_description\": \"GeI4 was synthesized from GeO2 and HI, and CH3NH3I was synthesized by reacting equimolar amounts of HI and CH3NH2.\\r\\nFor the synthesis of CH3NH3GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, CH3NH3I (159 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 \\u00b0C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements.  BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1 - R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01312\",\n        \"dataset_ID\": 529,\n        \"id\": 86,\n        \"compound_name\": \"2-dimethylamino-1-ethylamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N,N,N-dimethylethanaminium tetrabromoplumbate(II), (DMEN)PbBr4,2-(dimethylamino)ethylamine, ((CH3)2NH(CH2)2NH3)PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N,N,N-dimethylethanaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\\u03b1-(DMEN)PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"White-Light Emission and Structural Distortion in New Corrugated Two-Dimensional Lead Bromide Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5210\",\n        \"pages_end\": \"5215\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 2-(dimethylamino)ethylamine\",\n        \"synthesis_product\": \"pale yellow platelike crystals\",\n        \"synthesis_description\": \"0.669g PbO powder was added into 6.0 ml HBr and 1.0 mL of H3PO2 under stirring while heating at 150 \\u00b0C until PbO was dissolved. 0.264g 2-(dimethylamino)ethylamine was added to the above solution under heating and stirring. The \\u03b2-(DMEN)PbBr4 crystals were obtained during slow cooling.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation. Integration and correction of the data is done by STOE X-AREA programs. Crystal structures is resolved by using OLEX2 program package by full-matrix least-squares on F^2.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic5025795\",\n        \"dataset_ID\": 532,\n        \"id\": 93,\n        \"compound_name\": \"Bis(tropylium) tin iodide\",\n        \"formula\": \"C14H14SnI6\",\n        \"group\": \"Bis(tropylium) hexaiodostannate(IV), (C7H7)2SnI6\",\n        \"organic\": \"C7H7\",\n        \"inorganic\": \"SnI6, tin iodide\",\n        \"iupac\": \"bis(Tropylium) tin (IV) iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Inorganic\\u2212Organic Materials with an Optoelectronically Active Aromatic Cation: (C7H7)2SnI6 and C7H7PbI3\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"54\",\n        \"pages_start\": \"370\",\n        \"pages_end\": \"378\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"HI (57% aq., 1.5% H3PO2), tropylium tetrafluoroborate (99.99%, Sigma-Aldrich), tin metal shot (Sn, reagent grade, Alfa Aesar, iodine ( I2, 99.8%))\",\n        \"synthesis_product\": \"Black (C7H7)2SnI6 powder\",\n        \"synthesis_description\": \"SnI4 was synthesized in an evacuated fused silica ampule (P < 10 mTorr) by reacting Sn (2.62 mmol) and I2 (5.26 mmol) in a furnace at 200 \\u00b0C for 48 h.\\r\\nTropylium iodide was synthesized by reacting tropylium tetrafluoroborate (0.5177 g, 2.91 mmol) with HI.\\r\\nFor the preparation of (C7H7)2SnI6,  SnI4 (0.1834 g, 0.292 mmol) was dissolved in 7 mL HI in N2 atmosphere by heating at 100 \\u00b0C and stirring. To it tropylium iodide (0.1279 g, 0.586 mmol) was added. The solution was stirred for an additional 15 min, at which time the heat was removed and the flask was allowed to air-cool while stirring gently. The solution and precipitate were washed with anhydrous ether and centrifuged three times. The black product was dried at 37 \\u00b0C for 24 h.\",\n        \"experimental_method\": \"Powder X-ray diffraction + powder neutron diffraction\",\n        \"experimental_description\": \"PXRD data were obtained from the diffractometer on beamline 11-BM-B at the Advanced Photon Source, Argonne National Laboratory. Neutron diffraction data were collected at the Spallation Neutron Source (SNS) at the Oak Ridge National Laboratory using the POWGEN diffractometer (BL-11A).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"An\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b00847\",\n        \"dataset_ID\": 533,\n        \"id\": 98,\n        \"compound_name\": \"Bis(1-butylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"C11H39N5Pb4I13\",\n        \"group\": \"(BA)2(MA)3Pb4I13, bis(butane-1-aminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tris(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-10-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ruddlesden\\u2212Popper Hybrid Lead Iodide Perovskite 2D Homologous Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2853\",\n        \"pages_end\": \"2867\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",\n        \"synthesis_product\": \"Black plate-like (BA)2(MA)3Pb4I13 crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of HI solution (10.0 mL, 76 mmol) and  H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. \\r\\nSubsequent addition of solid CH3NH3Cl (507 mg, 7.5 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (248 \\u03bcL, 2.5 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution.\\r\\nAddition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time black rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after \\u223c2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b01025\",\n        \"dataset_ID\": 535,\n        \"id\": 95,\n        \"compound_name\": \"Guanidinium Germanium Iodide\",\n        \"formula\": \"CH6N3GeI3\",\n        \"group\": \"diaminomethanaminium triiodogermanate(II), C(NH2)3GeI3\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"GeI3, Germanium iodide\",\n        \"iupac\": \"diaminomethanaminium germanium (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Germanium Iodide Perovskite Semiconductors: Active Lone Pairs, Structural Distortions, Direct and Indirect Energy Gaps, and Strong Nonlinear Optical Properties\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"137\",\n        \"pages_start\": \"6804\",\n        \"pages_end\": \"6819\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), guanidinium chloride (C(NH2)3Cl, 98%)\",\n        \"synthesis_product\": \"yellow, elongated hexagonal tubular C(NH2)3GeI3 crystals\",\n        \"synthesis_description\": \"GeI4 was synthesized from GeO2 and HI, and C(NH2)3I was synthesized by reacting ethanolic solutions of C(NH)(NH2)2 (prepared by neutralizing C(NH2)3Cl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI. For the synthesis of C(NH2)3GeI3 aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, C(NH2)3I (183 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 \\u00b0C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1 - R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01312\",\n        \"dataset_ID\": 536,\n        \"id\": 97,\n        \"compound_name\": \"3-(dimethylamino)-1-propylamine lead bromide\",\n        \"formula\": \"C5H16N2PbBr4\",\n        \"group\": \"3-(N,N-dimethanaminium)-propane-1-aminium tetrabromoplumbate(II), (DMAPA)PbBr4, [(CH3)2NH(CH2)3NH3]PbBr4\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-(N,N-dimethanaminium)-propane-1-aminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"White-Light Emission and Structural Distortion in New Corrugated Two-Dimensional Lead Bromide Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5210\",\n        \"pages_end\": \"5215\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 3-(dimethylamino)-1-propylamine\",\n        \"synthesis_product\": \"pale yellow platelike crystal\",\n        \"synthesis_description\": \"0.892 g PbO powder was added to a mixture of 6.0 mL HBr and 1.0 mL H3PO2 under heating at 150\\u00b0C and stirring for about 10 mins until all PbO dissolved. Separately, 1.0 mL HBr was added to 0.408 g 3-(dimethylamino)-1-propylamine.\\r\\nThe solutions were mixed at 150\\u00b0C. During slow cooling, pale yellow platelike (DMAPA)PbBr4 crystals were formed.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation. Integration and correction of the data were done by STOE X-AREA programs. Crystal structures were resolved by using OLEX2 program package by full-matrix least-squares on F^2.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01312\",\n        \"dataset_ID\": 537,\n        \"id\": 99,\n        \"compound_name\": \"4-dimethylaminobutylamine lead bromide\",\n        \"formula\": \"C6H18N2PbBr4\",\n        \"group\": \"3-(N,N-dimethanaminium)-butane-1-aminium tetrabromoplumbate(II), (DMABA)PbBr4, [(CH3)2NH(CH2)4NH3]PbBr4\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-(N,N-dimethanaminium)-butane-1-aminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"White-Light Emission and Structural Distortion in New Corrugated Two-Dimensional Lead Bromide Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5210\",\n        \"pages_end\": \"5215\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), 48% hydrobromic acid (HBr), 50% aqueous H3PO2, 4-dimethylaminobutylaminee\",\n        \"synthesis_product\": \"pale yellow platelike crystal\",\n        \"synthesis_description\": \"0.892 g PbO powder was added to a mixture of 6.0 mL HBr and 1.0 mL H3PO2 under heating at 150\\u00b0C and stirring for about 10 mins until all PbO dissolved. Separately, 1.0 mL HBr was added to 0.500 g (4.3 mmol) of 4-dimethylaminobutylamine. The solutions were mixed at 150\\u00b0C. During slow cooling, pale yellow platelike (DMABA)PbBr4 crystals were formed.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction was collected by a STOE IPDS 2 or IPDS 2T diffractometer using graphite-monochromatized Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation. Integration and correction of the data were done by STOE X-AREA programs. Crystal structures were resolved by using OLEX2 program package by full-matrix least-squares on F^2.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aba2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b01025\",\n        \"dataset_ID\": 539,\n        \"id\": 94,\n        \"compound_name\": \"Acetamidinium Germanium Iodide\",\n        \"formula\": \"C2H7N2GeI3\",\n        \"group\": \"1-aminoethane-2-aminium triiodogermanate(II), CH3C(NH2)2GeI3\",\n        \"organic\": \"C2H7N2\",\n        \"inorganic\": \"GeI3, Germanium iodide\",\n        \"iupac\": \"1-aminoethane-2-aminium germanium (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Germanium Iodide Perovskite Semiconductors: Active Lone Pairs, Structural Distortions, Direct and Indirect Energy Gaps, and Strong Nonlinear Optical Properties\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"137\",\n        \"pages_start\": \"6804\",\n        \"pages_end\": \"6819\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), acetamidinium chloride (CH3C(NH2)2Cl, 98%)\",\n        \"synthesis_product\": \"yellow, elongated hexagonal tubular CH3C(NH2)2GeI3 crystals\",\n        \"synthesis_description\": \"GeI4 was synthesized from GeO2 and HI, and CH3C(NH2)2I was synthesized by reacting ethanolic solutions of CH3C(NH)(NH2) (prepared by neutralizing CH3C(NH2)2Cl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI. \\r\\nFor the synthesis of CH3C(NH2)2GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, CH3C(NH2)2I (184 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 \\u00b0C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1 - R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b00847\",\n        \"dataset_ID\": 540,\n        \"id\": 92,\n        \"compound_name\": \"Bis(1-butylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C10H36N4Pb3I10\",\n        \"group\": \"bis(butane-1-aminium) di(methanaminium) decaiodo triplumbate(II), (BA)2(MA)2Pb3I10\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) di(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-10-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ruddlesden\\u2212Popper Hybrid Lead Iodide Perovskite 2D Homologous Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2853\",\n        \"pages_end\": \"2867\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",\n        \"synthesis_product\": \"Dark red plate-like (BA)2(MA)2Pb3I10 crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of HI solution (10.0 mL, 76 mmol) and H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (450 mg, 6.67 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (327 \\u03bcL, 3.33 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which was subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time deep-red/purple rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after \\u223c2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"\",\n        \"label\": \"\",\n        \"space_group\": \"C2cb\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/ncomms14051\",\n        \"dataset_ID\": 541,\n        \"id\": 102,\n        \"compound_name\": \"N, N\\u2032-dimethylethylenediamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N, N\\u201a\\u00c4\\u2264-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N, N\\u2032-dimethylethylenediaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"One-dimensional organic lead halide perovskites with efficient bluish white-light emission\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"8\",\n        \"pages_start\": \"145051\",\n        \"pages_end\": \"145051\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 99.999%), N, N'-dimethylethylenediamine (99%), hydrobromic acid (HBr, 48 wt.% in H2O)\",\n        \"synthesis_product\": \"Colorless needle-like C4N2H14PbBr4 crystals\",\n        \"synthesis_description\": \"In 10\\u2009ml HBr, PbBr2 (0.100 g, 0.27 mmol) and N, N' -dimethylethylenediamine (0.024 g, 0.27 mmol) were dissolved by sonication for 10 minutes. 1 mL of this solution was kept in a vapor diffusion chamber. Acetone was diffused into this solution for 24 h.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected on a Bruker SMART APEX II diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"103.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imma\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201506449\",\n        \"dataset_ID\": 542,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, Single-Crystal Structure and Characterization of (CH3NH3)2Pb(SCN)2I2\",\n        \"journal\": \"Angewandte Correspondence\",\n        \"vol\": \"54\",\n        \"pages_start\": \"11016\",\n        \"pages_end\": \"11017\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Pb(SCN)2 (synthesized), methylammonium iodide (MAI, synthesized)\",\n        \"synthesis_product\": \"Dark red (or black) plate-like crystals\",\n        \"synthesis_description\": \"0.20 g Pb(SCN)2 and 0.15 g MAI were dissolved in 0.6 mL DMF and heated under stirring to 60 degrees C. Upon cooling and evaporation of DMF, the crystals precipitated from the solution.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data was collected using Bruker APEX II with CCD and micro-source and using Mo K\\u03b1 radiation (= 0.71073 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnm2(1)\",\n        \"extraction_method\": \"Data was manually extracted from the publication.\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b01025\",\n        \"dataset_ID\": 546,\n        \"id\": 105,\n        \"compound_name\": \"Tris(methylammonium) Germanium Iodide\",\n        \"formula\": \"C3H10NGeI3\",\n        \"group\": \"trimethanaminium triiodogermanate(II), (CH3)3NHGeI3, Trimethylammonium Germanium Iodide\",\n        \"organic\": \"C3H10N\",\n        \"inorganic\": \"GeI3, Germanium iodide\",\n        \"iupac\": \"trimethanaminium germanium (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Germanium Iodide Perovskite Semiconductors: Active Lone Pairs, Structural Distortions, Direct and Indirect Energy Gaps, and Strong Nonlinear Optical Properties\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"137\",\n        \"pages_start\": \"6804\",\n        \"pages_end\": \"6819\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), trimethylammonium chloride ((CH3)3NHCl, 98%)\",\n        \"synthesis_product\": \"pale yellow, elongated hexagonal tubular (CH3)3NHGeI3 crystals\",\n        \"synthesis_description\": \"GeI4 was synthesized from GeO2 and HI, and (CH3)3NHI was synthesized by reacting ethanolic solutions of (CH3)3N (prepared by neutralizing (CH3)3NHCl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI. For the synthesis of (CH3)3NHGeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, (CH3)3NHI (187 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 \\u00b0C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1 - R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P6(3)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 547,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation was used to collect the single crystal XRD data.\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic5025795\",\n        \"dataset_ID\": 548,\n        \"id\": 96,\n        \"compound_name\": \"Tropylium Lead Iodide\",\n        \"formula\": \"C7H7PbI3\",\n        \"group\": \"Tropylium triiodoplumbate(II), (C7H7)+PbI3\",\n        \"organic\": \"C7H7\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"tropylium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Inorganic\\u2212Organic Materials with an Optoelectronically Active Aromatic Cation: (C7H7)2SnI6 and C7H7PbI3\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"54\",\n        \"pages_start\": \"370\",\n        \"pages_end\": \"378\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"HI (57% aq., 1.5% H3PO2), tropylium tetrafluoroborate (99.99%, Sigma-Aldrich), lead iodide\\r\\n (PbI2), iodine ( I2, 99.8%))\",\n        \"synthesis_product\": \"Red C7H7PbI3 powder\",\n        \"synthesis_description\": \"For the preparation of C7H7PbI3, PbI2 (0.6438 g, 1.395 mmol) was dissolved in 11 mL HI in N2 atmosphere by heating at 45 \\u00b0C and stirring. The mixture was heated using an oil bath to 55 \\u00b0C and tropylium tetrafluoroborate (0.2483 g, 1.396 mmol) was added. The heating was stopped and the solution was allowed to cool under gentle stirring to 40 \\u00b0C. Then, the solution was taken out of N2 environment and was allowed to air cool in the oil bath. Once cool, the solution and red precipitate were washed with ethanol and centrifuged. The remaining product was then washed with anhydrous ether and centrifuged three times. The resulting bright red precipitate was dried at 37 \\u00b0C for 24 h.\",\n        \"experimental_method\": \"Powder X-ray diffraction + powder neutron diffraction\",\n        \"experimental_description\": \"PXRD data were obtained from the diffractometer on beamline 11-BM-B at the Advanced Photon Source, Argonne National Laboratory. Neutron diffraction data were collected at the Spallation Neutron Source (SNS) at the Oak Ridge National Laboratory using the POWGEN diffractometer (BL-11A).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b01025\",\n        \"dataset_ID\": 549,\n        \"id\": 106,\n        \"compound_name\": \"Isopropylammonium Germanium Iodide\",\n        \"formula\": \"C3H10NGeI3\",\n        \"group\": \"Isopropanaminium triiodogermanate(II), (CH3)2C(H)NH3GeI3, Isopropylammonium Germanium Iodide\",\n        \"organic\": \"C3H10N\",\n        \"inorganic\": \"GeI3, Germanium iodide\",\n        \"iupac\": \"Isopropanaminium germanium (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Germanium Iodide Perovskite Semiconductors: Active Lone Pairs, Structural Distortions, Direct and Indirect Energy Gaps, and Strong Nonlinear Optical Properties\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"137\",\n        \"pages_start\": \"6804\",\n        \"pages_end\": \"6819\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%),  Isopropylamine ((CH3)2C(H)NH2)\",\n        \"synthesis_product\": \"pale yellow, elongated hexagonal tubular (CH3)2C(H)NH3GeI3 crystals\",\n        \"synthesis_description\": \"GeI4 was synthesized from GeO2 and HI, and (CH3)2C(H)NH3I was synthesized by reacting equimolar amounts of HI and (CH3)2C(H)NH2. For the synthesis of (CH3)2C(H)NH3GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, (CH3)2C(H)NH3I (187 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 \\u00b0C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements. BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1 - R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"I-42d\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7tc04868h\",\n        \"dataset_ID\": 551,\n        \"id\": 100,\n        \"compound_name\": \"N-(3-aminopropyl)imidazole lead chloride\",\n        \"formula\": \"C6H13N3PbCl4\",\n        \"group\": \"N-(3-aminopropyl)imidazole tetrachloroplumbate(II),  3-(propane-1-aminium)imidazolium tetrachloroplumbate(II)\",\n        \"organic\": \"C6H13N3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"3-(propane-1-aminium)imidazolium lead (II) chloride\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Broadband white-light emission with a high color rendering index in a two-dimensional organic\\u2013inorganic hybrid perovskite\",\n        \"journal\": \"Journal of Materials Chemistry C\",\n        \"vol\": \"6\",\n        \"pages_start\": \"1171\",\n        \"pages_end\": \"1175\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"HCl (38%), methanol (99.5%), Pb(Ac)2.3H2O (99.5%), 1-(3-aminopropyl)imidazole (97%)\",\n        \"synthesis_product\": \"colorless plate-like crystals\",\n        \"synthesis_description\": \"Step1: fabrication of 1-(3-Aminopropyl)imidazole chloride:\\r\\n1:1 mole ratio of 1-(3-aminopropyl)imidazole and dilute aqueous HCl solution were mixed.\\r\\nBy volatilizing the solvent, the white powder 1-(3-aminopropyl)imidazole chloride was obtained. After recrystallization with methanol three times, the purified white powder was dried at 333 K in a vacuum oven for 48 h.\\r\\nStep2: Single-crystal growth for N-(3-aminopropyl)imidazole lead chloride\\r\\n3.79 g Pb(Ac)2.3H2O, and 1.98g 1-(3-aminopropyl)imidazole chloride were added into an aqueous HCl solution (38%, 150mL). After heating for 50 mins, the solution became clear. By slowly evaporating the solvent at room temperature for several weeks, colorless single crystals were produced.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction was collected using Bruker D8 diffractomenter by graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5). Data reduction and empirical absorption correction was done by Crystal Clear software. The crystal structure was resolved using SHELXTL software by full-matrix least squares on F^2 using SHELXTL-97.\",\n        \"physical_property\": \"298.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/acs.inorgchem.7b02285\",\n        \"dataset_ID\": 552,\n        \"id\": 107,\n        \"compound_name\": \"N,N-dimethylphenylene-p-diammonium lead iodide\",\n        \"formula\": \"C8H14N2PbI4\",\n        \"group\": \"benzene-1,4-di(methanaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C8H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"benzene-1,4-di(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead Halide Perovskites Templated by a Conjugated Asymmetric Diammonium\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"14991\",\n        \"pages_end\": \"14998\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Pb(CH3COO)2\\u00b73H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HI (57 wt % in H2O, stabilized with H3PO4, 99.95%), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",\n        \"synthesis_product\": \"Red block-like crystal\",\n        \"synthesis_description\": \"Pb(CH3COO)2\\u00b73H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HI and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at \\u221270 \\u00b0C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 \\u00d7 10 mL). The precipitate was redissolved in 5 mL of HI and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",\n        \"experimental_method\": \"Single crystal XRD\",\n        \"experimental_description\": \"a Bruker Quazar SMART APEXII diffractometer with Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation was used to collect the data.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b00248\",\n        \"dataset_ID\": 553,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Powder X-ray diffraction\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"2\\u03b8\",\n        \"secondary_unit\": \"(deg.)\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Photovoltaic Properties of Two-Dimensional (CH3NH3)2Pb(SCN)2I2 Perovskite: A Combined Experimental and Density Functional Theory Study\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"7\",\n        \"pages_start\": \"1213\",\n        \"pages_end\": \"1218\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CH3NH3I (MAI, Dyesol), Pb(SCN)2 (Aldrich)\",\n        \"synthesis_product\": \"dark-red (MA)2Pb(SCN)2I2 Powder\",\n        \"synthesis_description\": \"Stoichiometric amounts of MAI and Pb(SCN)2 were ground in a nitrogen-filled glovebox. The powdered mixture was then cold-pressed into a pellet. The pellet was flame-sealed under vacuum (\\u223c7 \\u00d7 10\\u22127 Torr) in a quartz tube. The reaction mixture was slowly heated to 100 \\u00b0C over 1 h and kept at this temperature for 20 h in a box furnace.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Data was recorded using a PANalytical Empyrean powder X-ray diffractometer (Cu K\\u03b1 radiation) under ambient conditions with the operating conditions of 40 kV and 44 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnm2(1)\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201406466\",\n        \"dataset_ID\": 554,\n        \"id\": 126,\n        \"compound_name\": \"bis(phenylethylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C18H36N4Pb3I10\",\n        \"group\": \"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) bismethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Layered Hybrid Perovskite Solar-Cell Absorber with Enhanced Moisture Stability\",\n        \"journal\": \"Angewandte Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"11232\",\n        \"pages_end\": \"11235\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"lead iodide (PbI2), phenyl ethyl ammonium iodide (PEAI; synthesized from phenyl ethyl amine and HI), methylammonium iodide (MAI; synthesized from methylamine and HI), sodium iodide (NaI), acetone, nitromethane\",\n        \"synthesis_product\": \"dark red plate-like (PEA)2(MA)2[Pb3I10] crystals\",\n        \"synthesis_description\": \"(PEA)I (3.60 mg, 0.0145 mmol), (MA)I (2.30 mg, 0.0145 mmol), and PbI2 (10.0 mg, 0.0217 mmol) were dissolved in a mixture of acetone (10 mL) and nitromethane (5 mL). NaI (6.50 mg, 0.0434 mmol) was added to this solution. The solvent was slowly evaporated for over 6 days to obtain the crystals.\",\n        \"experimental_method\": \"Single-crystal X- ray Diffraction\",\n        \"experimental_description\": \"Bruker D8 Venture diffractometer equipped with a Photon 100 CMOS detector and with monochromated Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/acs.inorgchem.7b02285\",\n        \"dataset_ID\": 555,\n        \"id\": 108,\n        \"compound_name\": \"N,N-dimethylphenylene-p-diammonium lead bromide\",\n        \"formula\": \"C8H14N2PbBr4\",\n        \"group\": \"benzene-1,4-di(methanaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C8H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"benzene-1,4-di(methanaminium) lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead Halide Perovskites Templated by a Conjugated Asymmetric Diammonium\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"14991\",\n        \"pages_end\": \"14998\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Pb(CH3COO)2\\u00b73H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HBr (48 wt % in H2O), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",\n        \"synthesis_product\": \"Yellow block-like crystal\",\n        \"synthesis_description\": \"Pb(CH3COO)2\\u00b73H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HBr and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at \\u221270 \\u00b0C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 \\u00d7 10 mL). The precipitate was redissolved in 5 mL of HBr and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"a Bruker Quazar SMART APEXII diffractometer with Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation was used to collect the data.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C8SC03863E\",\n        \"dataset_ID\": 556,\n        \"id\": 109,\n        \"compound_name\": \"Bis(2-ethyl-hexylammonium) lead iodide\",\n        \"formula\": \"C16H40N2PbI4\",\n        \"group\": \"bis(2-ethyl-1-hexanaminium) tetraiodoplumbate(II), (2-Et-ha)2PbI4\",\n        \"organic\": \"C8H20N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-ethyl-1-hexanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Melting temperature suppression of layered hybrid lead halide perovskites via organic ammonium cation branching\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1168\",\n        \"pages_end\": \"1175\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"2-Ethyl-1-hexylamine (2-Et-ha, 98%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",\n        \"synthesis_product\": \"clear orange plate-like crystal\",\n        \"synthesis_description\": \"2-Et-ha\\u2219HI salt was synthesized by adding a stoichiometric volume of HI into 2-Ethyl-1-hexylamine in a cold water bath, evaporating water at 150 \\u02daC on a hot plate and vacuum drying at 150 \\u02daC at 40 mtorr for a week. Thin plate-like (2-Et-ha)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-ha\\u2219HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data were collected using Bruker D8 ADVANCE Series II diffractometer using Mo K\\u03b1 radiation (= 0.71073 \\u00c5).\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C8SC03863E\",\n        \"dataset_ID\": 557,\n        \"id\": 87,\n        \"compound_name\": \"1-methyl-hexylammonium lead iodide\",\n        \"formula\": \"C14H36N2PbI4\",\n        \"group\": \"1-methyl-hexanaminium tetraiodoplumbate(II), [C14H36N2]PbI4, (1-Me-ha)2PbI4\",\n        \"organic\": \"C7H18N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-methyl-hexanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"2D hybrid organic-inorganic perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Melting temperature suppression of layered hybrid lead halide perovskites via organic ammonium cation branching\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1168\",\n        \"pages_end\": \"1175\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"2-Aminoheptane (1-Me-ha, 99%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",\n        \"synthesis_product\": \"Clear light orange plate-like crystals\",\n        \"synthesis_description\": \"1Me-ha\\u2219HI salt was synthesized by adding a stoichiometric volume of HI into  2-Aminoheptane in a cold water bath, evaporating water at 150 \\u02daC on a hot plate and vacuum drying at 150 \\u02daC at 40 mtorr for a week. Thin plate-like (1-Me-ha)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-ha\\u2219HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data were collected using Bruker D8 ADVANCE Series II diffractometer using Mo K\\u03b1 radiation (= 0.71073 \\u00c5).\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b00248\",\n        \"dataset_ID\": 558,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"cm^{-1}\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"Density functional theory\",\n        \"xc_functional\": \"HSE\",\n        \"k_point_grid\": \"2x6x6\",\n        \"level_of_relativity\": \"spin-orbit coupling included\",\n        \"basis_set_definition\": \"projector-augmented wave (PAW) method, plane-wave cutoff 500 eV\",\n        \"numerical_accuracy\": \"total force on each atom converged to <0.01 eV/\\u00c5 .\",\n        \"title\": \"Photovoltaic Properties of Two-Dimensional (CH3NH3)2Pb(SCN)2I2 Perovskite: A Combined Experimental and Density Functional Theory Study\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"7\",\n        \"pages_start\": \"1213\",\n        \"pages_end\": \"1218\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C8SC03863E\",\n        \"dataset_ID\": 560,\n        \"id\": 111,\n        \"compound_name\": \"bis(sec-butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"1-methyl-1-propanaminium tetraiodoplumbate(II), (1-Me-pa)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-methyl-1-propanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Melting temperature suppression of layered hybrid lead halide perovskites via organic ammonium cation branching\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1168\",\n        \"pages_end\": \"1175\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"sec-butylamine (1-Me-pa, 99%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",\n        \"synthesis_product\": \"metallic orange block\",\n        \"synthesis_description\": \"1-Me-pa\\u2219HI salt was synthesized by adding a stoichiometric volume of HI into sec-butylamine in a cold water bath, evaporating water at 150 \\u02daC on a hot plate and vacuum drying at 150 \\u02daC at 40 mtorr for a week. Thin plate-like (1-Me-pa)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-pa\\u2219HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data were collected using Rigaku XtaLAB Synergy-S diffractometer using Mo K\\u03b1 radiation (= 0.71073 \\u00c5).\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"P4(2)/ncm\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b00248\",\n        \"dataset_ID\": 561,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Photovoltaic Properties of Two-Dimensional (CH3NH3)2Pb(SCN)2I2 Perovskite: A Combined Experimental and Density Functional Theory Study\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"7\",\n        \"pages_start\": \"1213\",\n        \"pages_end\": \"1218\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 562,\n        \"id\": 115,\n        \"compound_name\": \"MeTz-PhMA2PbI4\",\n        \"formula\": \"C20H24N10PbI4\",\n        \"group\": \"(3-methyl-(p-tolyl)-1,2,4,5- tetrazine-6-)methanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C20H24N10\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"(3-methyl-(p-tolyl)-1,2,4,5- tetrazine-6-)methanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Energy Transfer to Small Band Gap Organic Cation in Two-Dimensional Organic-Inorganic Hybrid Perovskites Enables Multi-Color Emission\",\n        \"journal\": \"Submitted\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.93.094105\",\n        \"dataset_ID\": 563,\n        \"id\": 113,\n        \"compound_name\": \"ammonium tin iodide\",\n        \"formula\": \"NH4SnI3\",\n        \"group\": \"aminium triiodostannate(II), Ammonium Tin Iodide\",\n        \"organic\": \"NH4\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"aminium tin (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06\",\n        \"k_point_grid\": \"7 \\u00d7 7 \\u00d7 7\",\n        \"level_of_relativity\": \"spin-orbit coupling included\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered structures of organic/inorganic hybrid halide perovskites\",\n        \"journal\": \"PHYSICAL REVIEW B\",\n        \"vol\": \"93\",\n        \"pages_start\": \"094105-1\",\n        \"pages_end\": \"094105-6\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C8SC03863E\",\n        \"dataset_ID\": 564,\n        \"id\": 114,\n        \"compound_name\": \"bis(1-methyl-butylammonium) lead iodide\",\n        \"formula\": \"C10H30N2PbI4\",\n        \"group\": \"1-methyl-1-butanaminium tetraiodoplumbate(II), (1-Me-ba)2PbI4\",\n        \"organic\": \"C5H15N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-methyl-1-butanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Melting temperature suppression of layered hybrid lead halide perovskites via organic ammonium cation branching\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1168\",\n        \"pages_end\": \"1175\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"2-Aminopentane (1-Me-ba, 97%), hydriodic acid (HI) solution (57 wt%, stabilized, 99.95%), PbI2\",\n        \"synthesis_product\": \"clear orange plate-like crystals\",\n        \"synthesis_description\": \"1-Me-ba\\u2219HI salt was synthesized by adding a stoichiometric volume of HI into 2-Aminopentane in a cold water bath, evaporating water at 150 \\u02daC on a hot plate and vacuum drying at 150 \\u02daC at 40 mtorr for a week. Thin plate-like (1-Me-ba)2PbI4 crystals were grown by adding stoichiometric amounts of PbI2 (0.25 mmol) and 1-Me-ba\\u2219HI  (0.5 mmol) to a solution of 0.5 mL HI solution and 0.5 mL methanol followed by slow evaporation of the solution over a week. The crystals were filtered and washed with ethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data were collected using Bruker D8 ADVANCE Series II diffractometer using Mo K\\u03b1 radiation (= 0.71073 \\u00c5).\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 565,\n        \"id\": 116,\n        \"compound_name\": \"MeTz-PhMA2PbBr4\",\n        \"formula\": \"C20H24N10PbBr4\",\n        \"group\": \"(3-methyl-(p-tolyl)-1,2,4,5- tetrazine-6-)methanaminium tetrabromoplumbate(II), (3-methyl-(p-tolyl)-1,2,4,5- tetrazine-6-)methanaminium lead bromide\",\n        \"organic\": \"C20H24N10\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"(3-methyl-(p-tolyl)-1,2,4,5- tetrazine-6-)methanaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Energy Transfer to Small Band Gap Organic Cation in Two-Dimensional Organic-Inorganic Hybrid Perovskites Enables Multi-Color Emission\",\n        \"journal\": \"Submitted\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 566,\n        \"id\": 70,\n        \"compound_name\": \"Tris(2,6-dimethylpiperazine) lead bromide\",\n        \"formula\": \"C18H48N6Pb2Br10\",\n        \"group\": \"2,6-dimethyl-1,3-diazinanium decabromo diplumbate(II), (2,6-dmpz)3Pb2Br10, (C6H16N2)3Pb2Br10\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2Br10, Lead bromide\",\n        \"iupac\": \"2,6-dimethyl-1,3-diazinanium lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA package\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"revPBE-GGA\",\n        \"k_point_grid\": \"Energy cutoff of 150 Ry for real-space mesh size\",\n        \"level_of_relativity\": \"SOC on-site approximation as proposed by Fern\\u00e1ndez-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",\n        \"basis_set_definition\": \"Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier\\u2212Martins pseudopotentials\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 567,\n        \"id\": 71,\n        \"compound_name\": \"4-(aminomethyl)piperidine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"4-(methanaminium)piperidine tetrabromoplumbate(II), (4AMP)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperidine lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA package\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"revPBE-GGA\",\n        \"k_point_grid\": \"Energy cutoff of 150 Ry for real-space mesh size\",\n        \"level_of_relativity\": \"SOC on-site approximation as proposed by Fern\\u00e1ndez-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",\n        \"basis_set_definition\": \"Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier\\u2212Martins pseudopotentials\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 568,\n        \"id\": 72,\n        \"compound_name\": \"1-ethylpiperazine lead bromide\",\n        \"formula\": \"C6H16N2PbBr4\",\n        \"group\": \"1-ethane-1,3-diazinanium tetrabromoplumbate(II), (epz)PbBr4, (C6H16N2)PbBr4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-ethane-1,3-diazinanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA package\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"revPBE-GGA\",\n        \"k_point_grid\": \"Energy cutoff of 150 Ry for real-space mesh size\",\n        \"level_of_relativity\": \"SOC on-site approximation as proposed by Fern\\u00e1ndez-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",\n        \"basis_set_definition\": \"Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier\\u2212Martins pseudopotentials\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b08691\",\n        \"dataset_ID\": 569,\n        \"id\": 76,\n        \"compound_name\": \"Heptamethylenimine lead bromide\",\n        \"formula\": \"C7H16NPbBr3\",\n        \"group\": \"Heptamethylenimine tribromoplumbate(II), (hep)PbBr3, (C7H16N)PbBr3\",\n        \"organic\": \"C7H16N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azocanium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA package\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"revPBE-GGA\",\n        \"k_point_grid\": \"Energy cutoff of 150 Ry for real-space mesh size\",\n        \"level_of_relativity\": \"SOC on-site approximation as proposed by Fern\\u00e1ndez-Seivane et al. (J. Phys.: Condens. Matter 2006, 18, 7999)\",\n        \"basis_set_definition\": \"Double-zeta polarized basis set of finite-range numerical pseudoatomic orbitals; Troullier\\u2212Martins pseudopotentials\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Diversity in White-Light-Emitting Hybrid Lead Bromide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"13078\",\n        \"pages_end\": \"13088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201806452\",\n        \"dataset_ID\": 570,\n        \"id\": 117,\n        \"compound_name\": \"Cesium tin bromide (0D)\",\n        \"formula\": \"Cs4SnBr6\",\n        \"group\": \"tetracesium hexabromostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Emissive Self-Trapped Excitons in Fully Inorganic Zero- Dimensional Tin Halides\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"11329\",\n        \"pages_end\": \"11333\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Cesium bromide (CsBr, 99%, Alfa Aesar), tin (II) bromide (SnBr2, 99.2%, Alfa Aesar)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Mix CsBr and SnBr2 in a 4.5:1 molar ratio, mortar, and press together into a pellet (> 5 tons of pressure, 12 mm die). Seal pellet under vacuum (10-2 \\u2013 10-3 mbar) in a Pyrex tube and heat to 350 \\u00b0C for 60 hours. Open tube in the glovebox, and repeat the process until the formation of single crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"XtraLAB Synergy, Dualflex, Pilatus 300K diffractometer. PhotonJet (Cu) X-ray source (CuK\\u03b1, \\u03bb=1.54184 \\u00c5; micro-focus sealed X-ray tube) and mirror monochromator. Data processed and refined with CrysAlis PRO 1.171.39.31d (Rigaku OD, 2017), SHELXS, XL, and Olex2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201806452\",\n        \"dataset_ID\": 571,\n        \"id\": 118,\n        \"compound_name\": \"Cesium tin iodide (0D)\",\n        \"formula\": \"Cs4SnI6\",\n        \"group\": \"tetracesium hexaiodostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Emissive Self-Trapped Excitons in Fully Inorganic Zero- Dimensional Tin Halides\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"11329\",\n        \"pages_end\": \"11333\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Cesium bromide (CsBr, 99%), tin (II) iodide (SnI2, 99%)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"Mix CsBr and SnI2 in a 4.5:1 molar ratio, mortar, and press together into a pellet (> 5 tons of pressure, 12 mm die). Seal pellet under vacuum (10-2 \\u2013 10-3 mbar) in a Pyrex tube and heat to 350 \\u00b0C for 60 hours. Open tube in the glovebox, and repeat the process until the formation of single crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"XtraLAB Synergy, Dualflex, Pilatus 300K diffractometer. PhotonJet (Cu) X-ray source (CuK\\u03b1, \\u03bb=1.54184 \\u00c5; micro-focus sealed X-ray tube) and mirror monochromator. Data processed and refined with CrysAlis PRO 1.171.39.31d (Rigaku OD, 2017), SHELXS, XL, and Olex2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsenergylett.8b00661\",\n        \"dataset_ID\": 588,\n        \"id\": 119,\n        \"compound_name\": \"N, N\\u2032-dimethylethylenediamine lead chloride\",\n        \"formula\": \"C4H14N2PbCl4\",\n        \"group\": \"N, N\\u201a\\u00c4\\u2264-dimethylethylenediaminium tetrachloroplumbate(II)\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"N, N\\u2032-dimethylethylenediaminium lead (II) chloride\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A One-Dimensional Organic Lead Chloride Hybrid with Excitation-Dependent Broadband Emissions\",\n        \"journal\": \"ACS Energy Letters\",\n        \"vol\": \"3\",\n        \"pages_start\": \"1443\",\n        \"pages_end\": \"1449\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydrochloric acid (HCl, 37 wt. % in H2O), N, N\\u2019-dimethylethylenediamine (99%), Lead (II) chloride (PbCl2, 99.99%)\",\n        \"synthesis_product\": \"Colorless platelet-like crystals\",\n        \"synthesis_description\": \"To grow C4N2H14PbCl4 single crystals, dissolve lead (II) chloride (150 mg, 0.54 mmol) and N, N\\u2019-dimethylethylene-1,2-diammonium chloride (43.7 mg, 0.27 mmol) in DMSO to form a clear precursor solution. Diffuse single crystal into precursor solution for one day. Wash with acetone and dry in vacuum.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation. \\r\\nCool to 100 K with an Oxford-Diffraction Cryojet. \\r\\nPost-processing: Oxford-Diffraction CrysAlisPro software, CRYSTALS13, employing Superflip14 to solve the crystal structure.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imma\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsami.7b12862\",\n        \"dataset_ID\": 589,\n        \"id\": 120,\n        \"compound_name\": \"tetrakis(N,N\\u2032-dimethylethylene-1,2-diammonium-bromo) tin bromide iodide\",\n        \"formula\": \"(C16H52N8Br4SnBr3I3\",\n        \"group\": \"tetrakis(N,N\\u201a\\u00c4\\u2264-dimethylethylene-1,2-diaminium-bromo) tribromo-triiodostannate(II)\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr3I3, Tin bromide iodide\",\n        \"iupac\": \"tetrakis(N,N\\u2032-dimethylethylene-1,2-diaminium-bromo) tin bromide iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Broadband Yellow Phosphor Based on Zero-Dimensional Tin Mixed-Halide Perovskite\",\n        \"journal\": \"ACS Applied Materials & Interfaces\",\n        \"vol\": \"9\",\n        \"pages_start\": \"44579\",\n        \"pages_end\": \"44583\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Tin (II) bromide, Tin (II) iodide, N,N\\u2019-dimethylethylenediamine (99 %), hydrobromic acid (48 wt. % in H2O), hydriodic acid (55%), dichloromethane (DCM, 99.9 %), dimethylformamide (DMF, 99.8 %), toluene (anhydrous, 99.8 %)\",\n        \"synthesis_product\": \"Large yellow crystals\",\n        \"synthesis_description\": \"To prepare N,N\\u2019-dimethylethylene-1,2-diammonium bromide salts, add hydrobromic acid solution (2.2 equiv, 48%) into N,N\\u2019 dimethylethylenediamine (1 equiv) in ethanol at 0 C. Remove the solvents and starting reagents under vacuum, and wash the residue with ethyl ether. Dry salts and keep in a desiccator for future use. Prepare N,N\\u2019-dimethylethylene-1,2-diammonium iodide salts in a similar manner.\\r\\n\\r\\nTo prepare (C4N2H14Br)4SnBr3I3, mix tin(II) bromide and N,N\\u2019-dimethylethylene-1,2-diammonium bromide at 1:4 molar ratio and dissolve in DMF to form a clear solution. Mix tin(II) iodide and N,N\\u2019-dimethylethylene-1,2-diammonium iodide at 1:4 molar ratio and dissolve in DMF to form another clear solution. Mix bromide and iodide solutions at 1:1 to form a precursor solution. Prepare bulk single crystal by diffusing DCM into DMF solution at room temperature overnight. Wash the large yellowish crystals with acetone and dry under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation. \\r\\nMounted in a cryoloop under Paratone-N oil and cooled to 120 K with an Oxford-Diffraction Cryojet. \\r\\nPost processing: Oxford-Diffraction CrysAlisPro software, CRYSTALS.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1107/S0108270106039746\",\n        \"dataset_ID\": 590,\n        \"id\": 121,\n        \"compound_name\": \"1,4-phenyldiammonium lead iodide dihydrate\",\n        \"formula\": \"C6H10N2PbI4-2H2O\",\n        \"group\": \"1,4-phenyldiaminium tetraiodoplumbate(II) dihydrate, H3NC6H4NH3PbI4-2H2O\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1,4-phenyldiaminium lead iodide dihydrate\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two packing motifs based upon chains of edge-sharing PbI6 octahedra\",\n        \"journal\": \"Acta Crystallographica Section C\",\n        \"vol\": \"C62\",\n        \"pages_start\": \"m597\",\n        \"pages_end\": \"m601\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, HI, NH2C6H4NH2\",\n        \"synthesis_product\": \"Brown polyhedral crystals\",\n        \"synthesis_description\": \"Dissolve PbI2 (0.200 g, 0.434 mmol) in 47% HI (7 ml) in a test tube. Add NH2C6H4NH2 (0.043 g, 0.398 mmol) and dissolve the resulting precipitate via reflux for 12 h at 393 K. Cool the solution slowly to room temperature at a rate of 2 K h-1.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using a Bruker SMART CCD area-detector diffractometer with Mo Ka radiation\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnnm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1107/S0108270106039746\",\n        \"dataset_ID\": 591,\n        \"id\": 122,\n        \"compound_name\": \"bis(3,5-dimethylanilinium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis\\u00ac\\u2260(3,5-dimethyl\\u00ac\\u2260anilinium) tetraiodoplumbate(II), (C6H3NH3(CH3)2)2PbI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(3,5-dimethylanilinium) lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two packing motifs based upon chains of edge-sharing PbI6 octahedra\",\n        \"journal\": \"Acta Crystallographica Section C\",\n        \"vol\": \"C62\",\n        \"pages_start\": \"m597\",\n        \"pages_end\": \"m601\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C8H9NH2\",\n        \"synthesis_product\": \"Yellow plate-like crystals\",\n        \"synthesis_description\": \"Dissolve PbI2 (0.060 g, 0.130 mmol) in 47% HI (2 ml) in a round-bottomed flask. Add C8H9NH2 (0.040 g, 0.330 mmol) and dissolve the resulting precipitate via reflux for 12 h at 363 K. Cool the solution slowly to room temperature at a rate of 2 K h-1.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using a Bruker SMART CCD area-detector diffractometer with Mo Ka radiation\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/science.267.5203.1473\",\n        \"dataset_ID\": 592,\n        \"id\": 123,\n        \"compound_name\": \"Diiodoformamidinium bis(methylammonium) tin iodide\",\n        \"formula\": \"C4H20I2N5Sn2I8\",\n        \"group\": \"diiododiaminomethanide bis(methanaminium) bis(tetraiodostannate(II)), [NH2C(I)=NH2]2(CH3NH3)2Sn2I8\",\n        \"organic\": \"CH4IN2, CH6N\",\n        \"inorganic\": \"Sn2I8, Tin iodide\",\n        \"iupac\": \"diiododiaminomethanide bis(methanaminium)\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Conducting Layered Organic-Inorganic Halides Containing <110>-Oriented Perovskite Sheets\",\n        \"journal\": \"Science\",\n        \"vol\": \"267\",\n        \"pages_start\": \"1473\",\n        \"pages_end\": \"1476\",\n        \"year\": \"1995\",\n        \"synthesis_starting_materials\": \"CH3NH2\\u2022Hl, NH2CN, Snl2, HI\",\n        \"synthesis_product\": \"Crystals\",\n        \"synthesis_description\": \"CH3NH2\\u2022Hl (2.772 g, 17.44 mmol), NH2CN (0.733 g, 17.44 mmol), and Snl2 (6.495 g, 17.44 mmol) were dissolved in 70 ml of 57 weight % aqueous HI solution at 80\\u00b0C. After soaking at 80\\u00b0C for 12 hours, the solution was cooled to -10\\u00b0C at 2\\u00b0C/hour. The product was filtered under nitrogen, dried in flowing argon at 80\\u00b0C for several hours, and then removed to an argon-filled dry box with oxygen and water levels maintained at <1 part per million.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius CAD4 single-crystal diffractometer and graphite monochromatized MoKa radiation.\",\n        \"physical_property\": \"295.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/science.267.5203.1473\",\n        \"dataset_ID\": 593,\n        \"id\": 124,\n        \"compound_name\": \"Diiodoformamidinium tris(methylammonium) tin iodide\",\n        \"formula\": \"C5H26I2N7Sn3I11\",\n        \"group\": \"diiododiaminomethanide tris(methanaminium) tris(tetraiodostannate(II)), [NH2C(I)=NH2]2(CH3NH3)3Sn3I11\",\n        \"organic\": \"CH4IN2, CH6N\",\n        \"inorganic\": \"Sn3I11, Tin iodide\",\n        \"iupac\": \"diiododiaminomethanide tris(methanaminium)\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Conducting Layered Organic-Inorganic Halides Containing <110>-Oriented Perovskite Sheets\",\n        \"journal\": \"Science\",\n        \"vol\": \"267\",\n        \"pages_start\": \"1473\",\n        \"pages_end\": \"1476\",\n        \"year\": \"1995\",\n        \"synthesis_starting_materials\": \"CH3NH2\\u2022Hl, NH2CN, Snl2, HI\",\n        \"synthesis_product\": \"Sheet-like crystals\",\n        \"synthesis_description\": \"Prepare a 2:5:5 molar ratio of NH2CN, CH3NH2\\u2022HI, and Snl2 dissolved in 70 ml of 57 weight % aqueous HI solution at 80\\u00b0C. After soaking at 80\\u00b0C for 12 hours, the solution was cooled to -10\\u00b0C at 2\\u00b0C/hour. The product was filtered under nitrogen, dried in flowing argon at 80\\u00b0C for several hours, and then removed to an argon-filled dry box with oxygen and water levels maintained at <1 part per million. The product contained a mixture of [NH2C(I)=NH2]2(CH3NH3)3Sn3I11 and CH3NH2Snl3. The sheet-like [NH2C(I)=NH2]2(CH3NH3)3Sn3I11 crystals could be mechanically separated from the rod-like or rhombic dodecahedral cubic perovskite crystals because of the very different crystalline habit for these two materials.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius CAD4 single-crystal diffractometer and graphite monochromatized MoKa radiation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/science.267.5203.1473\",\n        \"dataset_ID\": 594,\n        \"id\": 125,\n        \"compound_name\": \"Diiodoformamidinium tetrakis(methylammonium) tin iodide\",\n        \"formula\": \"C6H32I2N8Sn4I14\",\n        \"group\": \"[NH2C(I)=NH2]2(CH3NH3)4Sn4I14, diiododiaminomethanide tetrakis(methanaminium) tetradecaiodo tetrastannate(II)\",\n        \"organic\": \"CH4IN2, CH6N\",\n        \"inorganic\": \"Sn4I14, Tin iodide\",\n        \"iupac\": \"diiododiaminomethanide tetrakis(methanaminium)\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Conducting Layered Organic-Inorganic Halides Containing <110>-Oriented Perovskite Sheets\",\n        \"journal\": \"Science\",\n        \"vol\": \"267\",\n        \"pages_start\": \"1473\",\n        \"pages_end\": \"1476\",\n        \"year\": \"1995\",\n        \"synthesis_starting_materials\": \"CH3NH2\\u2022Hl, NH2CN, Snl2, HI\",\n        \"synthesis_product\": \"Sheet-like crystals\",\n        \"synthesis_description\": \"Add large excess of CH3NH2\\u2022HI and Snl2 to NH2CN dissolved in 70 ml of 57 weight % aqueous HI solution at 80\\u00b0C. After soaking at 80\\u00b0C for 12 hours, the solution was cooled to -10\\u00b0C at 2\\u00b0C/hour. The product was filtered under nitrogen, dried in flowing argon at 80\\u00b0C for several hours, and then removed to an argon-filled dry box with oxygen and water levels maintained at <1 part per million. The [NH2C(I)=NH2]2(CH3NH3)4Sn4I14 crystals could be mechanically separated from the rod-like or rhombic dodecahedral cubic perovskite crystals because of the very different crystalline habit for these two materials.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius CAD4 single-crystal diffractometer and graphite monochromatized MoKa radiation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b00847\",\n        \"dataset_ID\": 595,\n        \"id\": 92,\n        \"compound_name\": \"Bis(1-butylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C10H36N4Pb3I10\",\n        \"group\": \"bis(butane-1-aminium) di(methanaminium) decaiodo triplumbate(II), (BA)2(MA)2Pb3I10\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) di(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-10-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBEsol\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"fully relaxed the internal atomic positions until the forces were less than 1 meV \\u00c5\\u22121 using a 500 eV plane-wave cutoff\",\n        \"title\": \"Ruddlesden\\u2212Popper Hybrid Lead Iodide Perovskite 2D Homologous Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2853\",\n        \"pages_end\": \"2867\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (450 mg, 6.67 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (327 \\u03bcL, 3.33 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which was subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time deep-red/purple rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after \\u223c2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"C2cb\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b00847\",\n        \"dataset_ID\": 596,\n        \"id\": 98,\n        \"compound_name\": \"Bis(1-butylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"C11H39N5Pb4I13\",\n        \"group\": \"(BA)2(MA)3Pb4I13, bis(butane-1-aminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tris(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-10-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBEsol\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"fully relaxed the internal atomic positions until the forces were less than 1 meV \\u00c5\\u22121 using a 500 eV plane-wave cutoff\",\n        \"title\": \"Ruddlesden\\u2212Popper Hybrid Lead Iodide Perovskite 2D Homologous Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2853\",\n        \"pages_end\": \"2867\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead Oxide (PbO), aqueous HI, aqueous H3PO2, n-CH3(CH2)3NH3I , solid CH3NH3Cl\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (507 mg, 7.5 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (248 \\u03bcL, 2.5 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time black rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after \\u223c2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction data were collected using an image plate STOE IPDS II diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Data reduction and numerical absorption corrections were performed using the X-AREA suite\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 597,\n        \"id\": 91,\n        \"compound_name\": \"3-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C6H16N2PbI4\",\n        \"group\": \"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (50 wt % in water)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from the publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 598,\n        \"id\": 91,\n        \"compound_name\": \"3-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C6H16N2PbI4\",\n        \"group\": \"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using either an STOE IPDS 2 or an IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from the publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 601,\n        \"id\": 110,\n        \"compound_name\": \"bis(2-phenethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C17H30N3Pb2I7\",\n        \"group\": \"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) methanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid, Lead oxide, Methylammonium Iodide, Phenylethylammonium\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"single crystals were grown using a previously reported cooling method. Briefly, precursors containing lead oxide, methylammonium iodide, and phenethylamine with specific ratios were dissolved in hydriodic. acid (HI) solution (57% w/w in water) at \\u223c90 \\u00b0C. The solution was then slowly cooled to room temperature at a rate of 1 \\u00b0C/h. The ratios are 1.72/0/3.45 mmol, 6/18/1 mmol, and 10/24/1 mmol for n = 1, 2, 3, respectively, in 30 mL of HI solution. It is worth noting that larger n-members (n > 3) of this 2D perovskite family can be also grown but in a mixture form, which should be caused by a large solubility difference between PEA and MA in the aqueous solution. MAPbI3 and MAPbBr3 single crystals were grown as previously reported.46 As-grown crystals were rinsed with diethyl ether and then dried under vacuum.\",\n        \"experimental_method\": \"Single crystal XRD\",\n        \"experimental_description\": \"XRD was carried out with a Bruker D8\\r\\nAdvance using a Cu K\\u03b11 (\\u03bb = 1.5406 \\u00c5) source, a step size of\\r\\n0.02\\u00b0, and a speed of 0.5 s/step. The absorption spectra were\\r\\ncaptured by measuring the diffuse reflectance spectra of crystal\\r\\npowders using a Cary 5000 (Agilent Technologies).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 602,\n        \"id\": 110,\n        \"compound_name\": \"bis(2-phenethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C17H30N3Pb2I7\",\n        \"group\": \"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) methanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"Including scaler relativistic\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"Single-particle wave functions (charges) were expanded on a plane-wave basis set up to a kinetic energy cutoff of 50 Ry (300 Ry). The crystal structures were fully relaxed until the total force on each atom was less than 0.01 eV/\\u00c5\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid, Lead oxide, Methylammonium Iodide, Phenylethylammonium\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"single crystals were grown using a previously reported cooling method. Briefly, precursors containing lead oxide, methylammonium iodide, and phenethylamine with specific ratios were dissolved in hydriodic. acid (HI) solution (57% w/w in water) at \\u223c90 \\u00b0C. The solution was then slowly cooled to room temperature at a rate of 1 \\u00b0C/h. The ratios are 1.72/0/3.45 mmol, 6/18/1 mmol, and 10/24/1 mmol for n = 1, 2, 3, respectively, in 30 mL of HI solution. It is worth noting that larger n-members (n > 3) of this 2D perovskite family can be also grown but in a mixture form, which should be caused by a large solubility difference between PEA and MA in the aqueous solution. MAPbI3 and MAPbBr3 single crystals were grown as previously reported.46 As-grown crystals were rinsed with diethyl ether and then dried under vacuum.\",\n        \"experimental_method\": \"Single crystal XRD\",\n        \"experimental_description\": \"XRD was carried out with a Bruker D8\\r\\nAdvance using a Cu K\\u03b11 (\\u03bb = 1.5406 \\u00c5) source, a step size of\\r\\n0.02\\u00b0, and a speed of 0.5 s/step. The absorption spectra were\\r\\ncaptured by measuring the diffuse reflectance spectra of crystal\\r\\npowders using a Cary 5000 (Agilent Technologies).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 604,\n        \"id\": 110,\n        \"compound_name\": \"bis(2-phenethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C17H30N3Pb2I7\",\n        \"group\": \"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) methanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2012\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",\n        \"synthesis_product\": \"Red (PEA)2MAPb2I7 crystals\",\n        \"synthesis_description\": \"6 mmol PbO, 18 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 \\u00b0C. The vial was then kept in an oven at 110 \\u00b0C for 4 h. The solution was then slowly cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"For steady-state PL measurements, the details are not available in the paper.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 607,\n        \"id\": 126,\n        \"compound_name\": \"bis(phenylethylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C18H36N4Pb3I10\",\n        \"group\": \"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) bismethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"Including scaler relativistic\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"Single-particle wave functions (charges) were expanded on a plane-wave basis set up to a kinetic energy cutoff of 50 Ry (300 Ry). The crystal structures were fully relaxed until the total force on each atom was less than 0.01 eV/\\u00c5\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",\n        \"synthesis_product\": \"Black (PEA)2MA2Pb3I10 crystals\",\n        \"synthesis_description\": \"10 mmol PbO, 24 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 \\u00b0C. The vial was then kept in an oven at 110 \\u00b0C for 4 h. The solution was then slowly cooled to room temperature.\",\n        \"experimental_method\": \"Single crystal XRD\",\n        \"experimental_description\": \"XRD was carried out with a Bruker D8\\r\\nAdvance using a Cu K\\u03b11 (\\u03bb = 1.5406 \\u00c5) source, a step size of\\r\\n0.02\\u00b0, and a speed of 0.5 s/step. The absorption spectra were\\r\\ncaptured by measuring the diffuse reflectance spectra of crystal\\r\\npowders using a Cary 5000 (Agilent Technologies).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 608,\n        \"id\": 126,\n        \"compound_name\": \"bis(phenylethylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C18H36N4Pb3I10\",\n        \"group\": \"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) bismethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"Including scaler relativistic\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"Single-particle wave functions (charges) were expanded on a plane-wave basis set up to a kinetic energy cutoff of 50 Ry (300 Ry). The crystal structures were fully relaxed until the total force on each atom was less than 0.01 eV/\\u00c5\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid, Lead oxide, Methylammonium Iodide, Phenylethylammonium\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"single crystals were grown using a previously reported cooling method. Briefly, precursors containing lead oxide, methylammonium iodide, and phenethylamine with specific ratios were dissolved in hydriodic. acid (HI) solution (57% w/w in water) at \\u223c90 \\u00b0C. The solution was then slowly cooled to room temperature at a rate of 1 \\u00b0C/h. The ratios are 1.72/0/3.45 mmol, 6/18/1 mmol, and 10/24/1 mmol for n = 1, 2, 3, respectively, in 30 mL of HI solution. It is worth noting that larger n-members (n > 3) of this 2D perovskite family can be also grown but in a mixture form, which should be caused by a large solubility difference between PEA and MA in the aqueous solution. MAPbI3 and MAPbBr3 single crystals were grown as previously reported.46 As-grown crystals were rinsed with diethyl ether and then dried under vacuum.\",\n        \"experimental_method\": \"Single crystal XRD\",\n        \"experimental_description\": \"XRD was carried out with a Bruker D8\\r\\nAdvance using a Cu K\\u03b11 (\\u03bb = 1.5406 \\u00c5) source, a step size of\\r\\n0.02\\u00b0, and a speed of 0.5 s/step. The absorption spectra were\\r\\ncaptured by measuring the diffuse reflectance spectra of crystal\\r\\npowders using a Cary 5000 (Agilent Technologies).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsphotonics.8b00052\",\n        \"dataset_ID\": 609,\n        \"id\": 127,\n        \"compound_name\": \"Bis(cyclohexylammonium) cadmium bromide\",\n        \"formula\": \"C12H28N2CdBr4\",\n        \"group\": \"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"CdBr4, Cadmium bromide\",\n        \"iupac\": \"bis(cyclohexylammonium) cadmium bromide\",\n        \"last_update\": \"2022-06-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Broadband Emission in a New Two-Dimensional Cd-Based Hybrid Perovskite\",\n        \"journal\": \"ACS Photonics\",\n        \"vol\": \"5\",\n        \"pages_start\": \"1599\",\n        \"pages_end\": \"1611\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, HBr, CdBr2\",\n        \"synthesis_product\": \"Colorless millimeter-sized plate-like crystal\",\n        \"synthesis_description\": \"Step 1: synthesis of cyclohexylammonium salt C6H11NH2\\u00b7HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20\\u00b0C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. Step 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days.\",\n        \"experimental_method\": \"Single crystals X-ray diffraction\",\n        \"experimental_description\": \"Diffractometer is Oxford Diffraction, equipped with two dimensional ATLAS detector. Graphite monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Unit cell determination and data reduction was performed by CRYSALIS program suite51 on the full set of data. Crystal structure resolution was obtained using \\r\\nSHELXS software by direct method.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsphotonics.8b00052\",\n        \"dataset_ID\": 610,\n        \"id\": 127,\n        \"compound_name\": \"Bis(cyclohexylammonium) cadmium bromide\",\n        \"formula\": \"C12H28N2CdBr4\",\n        \"group\": \"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"CdBr4, Cadmium bromide\",\n        \"iupac\": \"bis(cyclohexylammonium) cadmium bromide\",\n        \"last_update\": \"2022-06-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Broadband Emission in a New Two-Dimensional Cd-Based Hybrid Perovskite\",\n        \"journal\": \"ACS Photonics\",\n        \"vol\": \"5\",\n        \"pages_start\": \"1599\",\n        \"pages_end\": \"1611\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, HBr, CdBr2\",\n        \"synthesis_product\": \"Colorless millimeter-sized plate-like crystal\",\n        \"synthesis_description\": \"Step 1: synthesis of cyclohexylammonium salt C6H11NH2\\u00b7HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20\\u00b0C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. \\r\\nStep 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days.\",\n        \"experimental_method\": \"Double monochromator with photomultiplier.\",\n        \"experimental_description\": \"A double monochromator U1000 equipped with a photomultiplier was used. The excitation wavelength was 325 nm (3.815 eV).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsphotonics.8b00052\",\n        \"dataset_ID\": 611,\n        \"id\": 127,\n        \"compound_name\": \"Bis(cyclohexylammonium) cadmium bromide\",\n        \"formula\": \"C12H28N2CdBr4\",\n        \"group\": \"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"CdBr4, Cadmium bromide\",\n        \"iupac\": \"bis(cyclohexylammonium) cadmium bromide\",\n        \"last_update\": \"2022-06-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Broadband Emission in a New Two-Dimensional Cd-Based Hybrid Perovskite\",\n        \"journal\": \"ACS Photonics\",\n        \"vol\": \"5\",\n        \"pages_start\": \"1599\",\n        \"pages_end\": \"1611\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, HBr, CdBr2, N,N-dimethylformamide solvent (DMF)\",\n        \"synthesis_product\": \"200 nm thick (C6H11NH3)2CdBr4 film\",\n        \"synthesis_description\": \"Step 1: synthesis of cyclohexylammonium salt C6H11NH2\\u00b7HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20\\u00b0C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. \\r\\nStep 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days.\\r\\nStep 3: 10mg single crystal (C6H11NH3)2CdBr4 was dissolved in 1 mL of DMF.  10 \\u03bcL of the above solution was spin-coated on a clean glass at 1500 rpm for 30s, The obtained film was then annealed in air at 80 \\u00b0C for 5 min to remove residual solvent.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"Adsorption spectra was measured by PerkinElmer (Lambda 950) spectrophotometer.  A coldfinger of a helium closed cycle cryostat was used to control the temperature of the samples.\",\n        \"physical_property\": \"12.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsphotonics.8b00052\",\n        \"dataset_ID\": 612,\n        \"id\": 127,\n        \"compound_name\": \"Bis(cyclohexylammonium) cadmium bromide\",\n        \"formula\": \"C12H28N2CdBr4\",\n        \"group\": \"bis(cyclohexylammonium) tetrabromocadmate(II), (C6H11NH3)2CdBr4\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"CdBr4, Cadmium bromide\",\n        \"iupac\": \"bis(cyclohexylammonium) cadmium bromide\",\n        \"last_update\": \"2022-06-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Broadband Emission in a New Two-Dimensional Cd-Based Hybrid Perovskite\",\n        \"journal\": \"ACS Photonics\",\n        \"vol\": \"5\",\n        \"pages_start\": \"1599\",\n        \"pages_end\": \"1611\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, HBr, CdBr2, N,N-dimethylformamide solvent (DMF)\",\n        \"synthesis_product\": \"200 nm thick (C6H11NH3)2CdBr4 film\",\n        \"synthesis_description\": \"Step 1: synthesis of cyclohexylammonium salt C6H11NH2\\u00b7HBr: Mix cyclohexylamine C6H11NH2 and HBr (47 wt %) at -20\\u00b0C under stirring for 20 min. cyclohexylammonium salt will be obtained after evaporating the water by heating. The final colorless product can be obtained after washing with diethyl ether and drying under vacuum. Step 2: Add stoichiometric amounts of CdBr2 (1 mmol, 272 mg) into the prepared cyclohexylammonium salt (2 mmol, 360 mg). The mixture is stirred in methanol solvent and is kept in dark at room temperature for 5 days. Step 3: 10mg single crystal (C6H11NH3)2CdBr4 was dissolved in 1 mL of DMF. 10 \\u03bcL of the above solution was spin-coated on a clean glass at 1500 rpm for 30s, The obtained film was then annealed in air at 80 \\u00b0C for 5 min to remove residual solvent.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"Adsorption spectra was measured by PerkinElmer (Lambda 950) spectrophotometer.  A coldfinger of a helium closed cycle cryostat was used to control the temperature of the samples.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc01663a\",\n        \"dataset_ID\": 614,\n        \"id\": 128,\n        \"compound_name\": \"2-methyl-1,5-diaminopentane lead bromide\",\n        \"formula\": \"C6H18N2PbBr4\",\n        \"group\": \"2-methyl-5-aminopentane-1-aminium tetrabromoplumbate(II), (2meptH2)PbBr4\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2-methyl-5-aminopentane-1-aminium lead (II) bromide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly e\\ufb03cient white-light emission in a polar two-dimensional hybrid perovskite\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4053\",\n        \"pages_end\": \"4056\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbAc2\\u00b73H2O, HBr solution, 2-methyl1,5-diaminopentane (2mept)\",\n        \"synthesis_product\": \"colorless plate-like crystals\",\n        \"synthesis_description\": \"Step1. Fabrication of (2meptH2)PbBr4 powder\\r\\n\\r\\n0.005 mol PbAc2\\u00b73H2O (1.8967 g) was added into 20 ml 47% HBr solution. Then 0.005 mol (0.5811 g) 2-methyl1,5-diaminopentane (2mept) was dropwise added into the above solution, under stirring and heating for 5mins. After cooling down to room temperature, and drying under vacuum, (2meptH2)PbBr4 powder will be obtained. \\r\\n\\r\\nStep2:  (2meptH2)PbBr4 single crystal fabrication by temperature-lowering method. \\r\\n\\r\\nPrepare a saturated solution of (2meptH2)PbBr4 at  50 ~ 55 \\u00b0C, and then preheated to  65 \\u00b0C in order to form a clear solution. Decrease temperature at a rate of 1.0 \\u00b0C/day, after 2 weeks colorless (2meptH2)PbBr4 will be obtained.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SuperNova diffractometer with graphite-monochromatized Mo K\\u03b1\\r\\nradiation (\\u03bb = 0.71073 \\u00c5) was used to get single-crystal X-ray diffraction  at 295 K. CrystalClear software was used to do data procession. SHELXLTL software package was used to resolve crystal structure in direct methods and crystal refined in full-matrix least-squares refinements.\",\n        \"physical_property\": \"295.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc01663a\",\n        \"dataset_ID\": 615,\n        \"id\": 128,\n        \"compound_name\": \"2-methyl-1,5-diaminopentane lead bromide\",\n        \"formula\": \"C6H18N2PbBr4\",\n        \"group\": \"2-methyl-5-aminopentane-1-aminium tetrabromoplumbate(II), (2meptH2)PbBr4\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2-methyl-5-aminopentane-1-aminium lead (II) bromide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly e\\ufb03cient white-light emission in a polar two-dimensional hybrid perovskite\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4053\",\n        \"pages_end\": \"4056\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbAc2\\u00b73H2O, HBr solution, 2-methyl1,5-diaminopentane (2mept)\",\n        \"synthesis_product\": \"colorless crystals\",\n        \"synthesis_description\": \"Step1. Fabrication of (2meptH2)PbBr4 powder - 0.005 mol PbAc2\\u00b73H2O (1.8967 g) was added into 20 ml 47% HBr solution. Then 0.005 mol (0.5811 g) 2-methyl1,5-diaminopentane (2mept) was dropwisely added to the above solution, under stirring and heating for 5 mins. After cooling down to room temperature, and dried under vacuum, (2meptH2)PbBr4 powder was obtained. Step2: (2meptH2)PbBr4 single crystal fabrication - prepare a saturated solution of (2meptH2)PbBr4 at 50 ~ 55 \\u00b0C, and then preheated to 65 \\u00b0C in order to form a clear solution. Decrease temperature at a rate of 1.0 \\u00b0C/day, after 2 weeks colorless (2meptH2)PbBr4 will be obtained.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Edinburgh FLS980 fluorescence spectrometer was used to get emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc01663a\",\n        \"dataset_ID\": 616,\n        \"id\": 128,\n        \"compound_name\": \"2-methyl-1,5-diaminopentane lead bromide\",\n        \"formula\": \"C6H18N2PbBr4\",\n        \"group\": \"2-methyl-5-aminopentane-1-aminium tetrabromoplumbate(II), (2meptH2)PbBr4\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"2-methyl-5-aminopentane-1-aminium lead (II) bromide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly e\\ufb03cient white-light emission in a polar two-dimensional hybrid perovskite\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4053\",\n        \"pages_end\": \"4056\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbAc2\\u00b73H2O, HBr solution, 2-methyl1,5-diaminopentane (2mept)\",\n        \"synthesis_product\": \"colorless crystals\",\n        \"synthesis_description\": \"Step1. Fabrication of (2meptH2)PbBr4 powder -  0.005 mol PbAc2\\u00b73H2O (1.8967 g) was added into 20 ml 47% HBr solution. Then 0.005 mol (0.5811 g) 2-methyl1,5-diaminopentane (2mept) was dropwisely added to the above solution, under stirring and heating for 5 mins. After cooling down to room temperature, and dried under vacuum, (2meptH2)PbBr4 powder was obtained. \\r\\nStep2: (2meptH2)PbBr4 single crystal fabrication - prepare a saturated solution of (2meptH2)PbBr4 at 50 ~ 55 \\u00b0C, and then preheated to 65 \\u00b0C in order to form a clear solution. Decrease temperature at a rate of 1.0 \\u00b0C/day, after 2 weeks colorless (2meptH2)PbBr4 will be obtained.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Perkin-Elmer Lambda 900 UV\\u2013Vis\\u2013NIR spectrophotometer was used to get the absorption spectrum at room temperature. BaSO4 was used as the 100% reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 617,\n        \"id\": 129,\n        \"compound_name\": \"bis(1-Dodecylammonium) lead iodide\",\n        \"formula\": \"C24H56N2PbI4\",\n        \"group\": \"bis(dodecane-1-aminium) tetraiodoplumbate(II), (C12H25NH3)2PbI4\",\n        \"organic\": \"C12H28N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(dodecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI, C12H25NH2, methanol, ethyl acetate\",\n        \"synthesis_product\": \"yellow plate-like crystal\",\n        \"synthesis_description\": \"0.048 g PbI2 (0.104 mmol) was added into 3 mL 47% HI. Then 0.030 g C12H25NH2 (0.162 mmol) was added into the above solution. The formed precipitation then dissolved into methanol (5 mL)\\u2013ethyl acetate (3 mL) mixture. The yellow single crystals were obtained by slow evaporation over a number of days.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data.\\r\\nSAINT-NT16 was used to do data reduction and cell refinement.  XPREP16 was used to determine space groups.  WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 618,\n        \"id\": 129,\n        \"compound_name\": \"bis(1-Dodecylammonium) lead iodide\",\n        \"formula\": \"C24H56N2PbI4\",\n        \"group\": \"bis(dodecane-1-aminium) tetraiodoplumbate(II), (C12H25NH3)2PbI4\",\n        \"organic\": \"C12H28N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(dodecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI, C12H25NH2, methanol, ethyl acetate\",\n        \"synthesis_product\": \"Orange plate-like crystal\",\n        \"synthesis_description\": \"0.048 g PbI2 (0.104 mmol) was added into 3 mL 47% HI. Then 0.030 g C12H25NH2 (0.162 mmol) was added into the above solution. The formed precipitation then dissolved into methanol (5 mL)\\u2013ethyl acetate (3 mL) mixture. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase-transition at higher temperature to obtain the orange monoclinic phase.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data.\\r\\nSAINT-NT16 was used to do data reduction and cell refinement.  XPREP16 was used to determine space groups.  WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"319.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 619,\n        \"id\": 130,\n        \"compound_name\": \"bis(1-tetradecylammonium) lead iodide\",\n        \"formula\": \"C28H64N2PbI4\",\n        \"group\": \"bis(tetradecane-1-aminium) tetraiodoplumbate(II), (C14H29NH3)2PbI4\",\n        \"organic\": \"C14H32N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(tetradecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",\n        \"synthesis_product\": \"yellow plate-like crystal\",\n        \"synthesis_description\": \"0.015 g PbI2 (0.104 mmol) was added  into 1 mL 47% HI. Then, 0.010 g C14H29NH2 (0.047 mmol) was added to the above solution. The formed precipitation was then dissolved into 5 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 620,\n        \"id\": 130,\n        \"compound_name\": \"bis(1-tetradecylammonium) lead iodide\",\n        \"formula\": \"C28H64N2PbI4\",\n        \"group\": \"bis(tetradecane-1-aminium) tetraiodoplumbate(II), (C14H29NH3)2PbI4\",\n        \"organic\": \"C14H32N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(tetradecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",\n        \"synthesis_product\": \"Red plate-like crystal\",\n        \"synthesis_description\": \"0.015 g PbI2 (0.104 mmol) was added  into 1 mL 47% HI. Then, 0.010 g C14H29NH2 (0.047 mmol) was added to the above solution. The formed precipitation was then dissolved into 5 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase transition at a higher temperature to obtain the red monoclinic phase.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"335.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 621,\n        \"id\": 131,\n        \"compound_name\": \"bis(1-hexadecylammonium) lead iodide\",\n        \"formula\": \"C32H72N2PbI4\",\n        \"group\": \"bis(hexadecane-1-aminium) tetraiodoplumbate(II), (C16H33NH3)2PbI4\",\n        \"organic\": \"C16H36N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexadecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",\n        \"synthesis_product\": \"yellow plate-like crystal\",\n        \"synthesis_description\": \"0.062 g PbI2 (0.134 mmol) was added into 1 mL 47% HI. Then, 0.009 g C16H33NH2 (0.037 mmol) was added to the above solution. The formed precipitation was then dissolved into 8 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 622,\n        \"id\": 131,\n        \"compound_name\": \"bis(1-hexadecylammonium) lead iodide\",\n        \"formula\": \"C32H72N2PbI4\",\n        \"group\": \"bis(hexadecane-1-aminium) tetraiodoplumbate(II), (C16H33NH3)2PbI4\",\n        \"organic\": \"C16H36N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexadecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",\n        \"synthesis_product\": \"Red plate-like crystal\",\n        \"synthesis_description\": \"0.062 g PbI2 (0.134 mmol) was added into 1 mL 47% HI. Then, 0.009 g C16H33NH2 (0.037 mmol) was added to the above solution. The formed precipitation was then dissolved into 8 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase transition at a higher temperature to obtain the red monoclinic phase.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"341.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 623,\n        \"id\": 132,\n        \"compound_name\": \"bis(1-octadecylammonium) lead iodide\",\n        \"formula\": \"C36H80N2PbI4\",\n        \"group\": \"bis(octadecane-1-aminium) tetraiodoplumbate(II), (C18H37NH3)2[PbI4]\",\n        \"organic\": \"C18H40N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(octadecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",\n        \"synthesis_product\": \"yellow plate-like crystal\",\n        \"synthesis_description\": \"0.033g PbI2 (0.072 mmol) was added  into 1 mL 47% HI. Then, 0.008 g C18H37NH2 (0.030 mmol) was added to the above solution. The formed precipitation was then dissolved into 15 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b805417g\",\n        \"dataset_ID\": 624,\n        \"id\": 132,\n        \"compound_name\": \"bis(1-octadecylammonium) lead iodide\",\n        \"formula\": \"C36H80N2PbI4\",\n        \"group\": \"bis(octadecane-1-aminium) tetraiodoplumbate(II), (C18H37NH3)2[PbI4]\",\n        \"organic\": \"C18H40N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(octadecane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4](n = 12, 14, 16 and 18)\",\n        \"journal\": \"New Journal of Chemistry\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1736\",\n        \"pages_end\": \"1746\",\n        \"year\": \"2008\",\n        \"synthesis_starting_materials\": \"PbI2, 47% HI,  C14H29NH2, ethyl acetate\",\n        \"synthesis_product\": \"orange-reddish plate-like crystal\",\n        \"synthesis_description\": \"0.033g PbI2 (0.072 mmol) was added into 1 mL 47% HI. Then, 0.008 g C18H37NH2 (0.030 mmol) was added to the above solution. The formed precipitation was then dissolved into 15 mL ethyl acetate. The yellow single crystals were obtained by slow evaporation over a number of days. The crystals undergo a phase transition at a higher temperature to obtain the orange-red monoclinic phase.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Apex II CCD diffractometer with graphite-monochromated Mo-Ka radiation (\\u03bb = 0.71073 \\u00c5) was used to get diffraction data. SAINT-NT16 was used to do data reduction and cell refinement. XPREP16 was used to determine space groups. WinGx17 Suite by direct methods using SHELXS9718 was used to resolve structure and the structure refinement was done by full-matrix least squares/difference Fourier techniques using SHELXL97.\",\n        \"physical_property\": \"348.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja00124a012\",\n        \"dataset_ID\": 625,\n        \"id\": 133,\n        \"compound_name\": \"Tris(iodoformamidinium) tin iodide\",\n        \"formula\": \"C3H12I3N6SnI5\",\n        \"group\": \"tris(iododiaminomethanide) pentaiodostannate(II),[NH2C(I)==NH2]3Snl5\",\n        \"organic\": \"CH4IN2\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(iododiaminomethanide) tin iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Characterization of [NH2C(I)==NH2]3Ml5 (M = Sn, Pb): Stereochemical Activity in Divalent Tin and Lead Halides Containing Single <110> Perovskite Sheets\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"117\",\n        \"pages_start\": \"5297\",\n        \"pages_end\": \"5302\",\n        \"year\": \"1995\",\n        \"synthesis_starting_materials\": \"NH2CN, Snl2, aqueous HI (57 wt%)\",\n        \"synthesis_product\": \"Column-like orange crystals\",\n        \"synthesis_description\": \"Dissolve 0.5 g of NH2CN (0.126 g, 3.0 mmol) and Snl2 (0.374 g, 1 mmol) in 10 mL of 57 wt % aqueous HI solution at 80 \\u00b0C. Cool the solution from 80 to -10 \\u00b0C at 2 \\u00b0C/h. Filter the crystalline products under nitrogen from which, obtain column-like orange crystals. Dry the products in flowing argon at 80 \\u00b0C for several hours and then remove to an argon-filled drybox with oxygen and water levels maintained below 1 ppm. Separate the orange crystals from the transparent iodoformamidinium iodide crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius CAD4 diffractometer with graphite monochromatized Mo Ka radiation (\\u03bb = 0.7093 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja00124a012\",\n        \"dataset_ID\": 626,\n        \"id\": 134,\n        \"compound_name\": \"Tris(iodoformamidinium) lead iodide\",\n        \"formula\": \"C3H12I3N6Pbl5\",\n        \"group\": \"tris(iododiaminomethanide) pentaiodoplumbate(II), [NH2C(I)==NH2]3Pbl5\",\n        \"organic\": \"CH4IN2\",\n        \"inorganic\": \"PbI5, Lead iodide\",\n        \"iupac\": \"tris(iododiaminomethanide) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Characterization of [NH2C(I)==NH2]3Ml5 (M = Sn, Pb): Stereochemical Activity in Divalent Tin and Lead Halides Containing Single <110> Perovskite Sheets\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"117\",\n        \"pages_start\": \"5297\",\n        \"pages_end\": \"5302\",\n        \"year\": \"1995\",\n        \"synthesis_starting_materials\": \"CH3NH2\\u2022HI, NH2CN, Pbl2, aqueous HI (57 wt%)\",\n        \"synthesis_product\": \"Yellow transparent crystals\",\n        \"synthesis_description\": \"Dissolve a 1:1:1 molar ratio of CH3NH2\\u2022HI (0.480 g, 3.02 mmol), NH2CN (0.127 g, 3.02 mmol), and Pbl2 (1.393 g, 3.02 mmol). Dissolve the reactants in 17 mL of 57 wt % aqueous hydriodic acid at 60\\u00b0C. Soak the solution at 60\\u00b0C for 24 h before cooling to -10\\u00b0C at 2\\u00b0C/h. Hold the crystals at -10\\u00b0C for 10 h, filter the crystals and dry.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius CAD4 diffractometer with graphite monochromatized Mo Ka radiation (\\u03bb = 0.7093 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1107/S1600536806013973\",\n        \"dataset_ID\": 627,\n        \"id\": 135,\n        \"compound_name\": \"Bis(propane-1,2-diammonium) lead iodide trihydrate\",\n        \"formula\": \"C6H24N4PbI6 3H2O\",\n        \"group\": \"Bis(propane-1,2-diaminium) hexabromoplumbate(II), trihydrate, [NH3CH2CH(NH3)CH3]2[PbI6]3H2O\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbI6, Lead iodide\",\n        \"iupac\": \"Bis(propane-1,2-diaminium) lead iodide trihydrate\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bis(propane-1,2-diammonium) hexaiodoplumbate(II) trihydrate\",\n        \"journal\": \"Acta Crystallographica\",\n        \"vol\": \"E62\",\n        \"pages_start\": \"m1103\",\n        \"pages_end\": \"m1105\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, HI, NH2CH2CH(NH2)CH3\",\n        \"synthesis_product\": \"Colourless crystal\",\n        \"synthesis_description\": \"Dissolve PbI2 (0.220\\u2005g, 0.477\\u2005mmol) in 47% HI (3\\u2005ml) in a round-bottomed flask. Add NH2CH2CH(NH2)CH3 (0.200\\u2005g, 2.70\\u2005mmol), dissolve the resulting precipitate by refluxing for 12\\u2005h\\u2005at 363\\u2005K. Slowly cool the solution to room temperature at 2\\u2005K/h.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker SMART CCD area-detector diffractometer with Mo K\\u03b1 radiation.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1107/S0108270106016167\",\n        \"dataset_ID\": 628,\n        \"id\": 136,\n        \"compound_name\": \"Bis\\u00ad(tert-butyl\\u00adammonium) lead iodide dihydrate\",\n        \"formula\": \"C8H24N2[PbI3]I 2H2O\",\n        \"group\": \"bis\\u00ac\\u2260(2-methylpropane-2-aminium) tetraiodoplumbate(II) dihydrate, (C4H12N)2[PbI3]I 2H2O\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"[PbI3]I, Lead iodide\",\n        \"iupac\": \"bis\\u00ad(2-methylpropane-2-aminium) lead (II) iodide dihydrate\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"catena-Poly[bis(tert-butylammonium) [plumbate(II)-tri-l-iodo] iodide dihydrate]\",\n        \"journal\": \"Acta Crystallographica\",\n        \"vol\": \"C62\",\n        \"pages_start\": \"m264\",\n        \"pages_end\": \"m266\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C(CH3)3NH2\",\n        \"synthesis_product\": \"Yellow needle-like crystal\",\n        \"synthesis_description\": \"Dissolve PbI2 (0.126\\u2005g, 0.273\\u2005mmol) in 47% HI (2\\u2005ml) in a sample vial. Thereafter, add C(CH3)3NH2 (0.050\\u2005g, 0.684\\u2005mmol) and dissolve the resulting precipitate by refluxing for 12\\u2005h at 363\\u2005K. Slowly cool the solution to room temperature at a rate of 2\\u2005K/h.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker SMART CCD area-detector diffractometer with Mo K\\u03b1 radiation.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1107/S0108270106009127\",\n        \"dataset_ID\": 630,\n        \"id\": 137,\n        \"compound_name\": \"Tetrakis(3-phenylpropylammonium) lead iodide\",\n        \"formula\": \"C36H52N4Pb3I10\",\n        \"group\": \"tetrakis(1-phenylpropane-3-aminium) decaiodo triplumbate(II), (C9H14N)4Pb3I10\",\n        \"organic\": \"C9H14N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"tetrakis(1-phenylpropane-3-aminium) lead iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"catena-Poly[tetra\\u00adkis(3-phenyl\\u00adpropyl\\u00adammonium) [iodo\\u00adplumbate(II)-tri-\\u03bc-iodo-plumbate(II)-tri-\\u03bc-iodo-iodo\\u00adplumbate(II)-di-\\u03bc-iodo]]\",\n        \"journal\": \"Acta Crystallographica\",\n        \"vol\": \"C62\",\n        \"pages_start\": \"m174\",\n        \"pages_end\": \"m176\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbO, 3-phenylpropylamine, HI\",\n        \"synthesis_product\": \"Yellow rectangular crystals\",\n        \"synthesis_description\": \"Dissolve PbO (0.184\\u2005g, 0.824\\u2005mmol) and 3-phenylpropylamine (0.167\\u2005g, 1.23\\u2005mmol) in HI (3\\u2005ml) and heat to form a clear solution. Slowly cool to room temperature to form yellow crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker SMART CCD area-detector diffractometer with Mo K\\u03b1 radiation\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/A608415J\",\n        \"dataset_ID\": 631,\n        \"id\": 138,\n        \"compound_name\": \"1,4-phenyldiammonium lead iodide tetrahydrofuran\",\n        \"formula\": \"C6H10N2Pb2I6 3THF\",\n        \"group\": \"1,4-benzenediaminium fluorolane bis(triiodoplumbate(II)), (C6H10N2)Pb2I6\\u00ac\\u22113THF\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"1,4-benzenediaminium fluorolane lead iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and structure of a new layered organic\\u2013inorganic compound containing unique chains of PbI2\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"7\",\n        \"pages_start\": \"697\",\n        \"pages_end\": \"698\",\n        \"year\": \"1997\",\n        \"synthesis_starting_materials\": \"p-nitroaniline, PbI2, HI (aq)/acetonitrile, THF\",\n        \"synthesis_product\": \"Orange parallelepiped crystals\",\n        \"synthesis_description\": \"React p-nitroaniline (0.59 g, 4.33 mmol) and lead(ii) iodide (1.00 g, 2.17 mmol) in 8 ml of concentrated 57 mass % aqueous hydriodic acid diluted with acetonitrile. Warm resulting solution to 60 \\u00b0C and slowly cool to 20 \\u00b0C during which the solution turns dark red-brown, and brown precipitate forms. Collect the precipitate and redissolve in tetrahydrofuran (THF) at 60 \\u00b0C. Slowly cool the resulting solution from 60 to -10\\u00b0C over 7 days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Monochromated Mo-Ka radiation, a stream of dry N2 gas at -50 \\u00b0C.\",\n        \"physical_property\": \"\\u2248223.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm010105g\",\n        \"dataset_ID\": 633,\n        \"id\": 141,\n        \"compound_name\": \"3-fluoro-2-phenethylammonium tin iodide\",\n        \"formula\": \"C16H22F2N2SnI4\",\n        \"group\": \"3-fluoro-2-phenylethanaminium tetraiodostannate(II), (3-FPEA)2SnI4, (C8H11FN)2(I4Sn)\",\n        \"organic\": \"C8H11FN\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3-fluoro-2-phenylethanaminium tin (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structurally Tailored Organic-Inorganic Perovskites: Optical Properties and Solution-Processed Channel Materials for Thin-Film Transistors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"13\",\n        \"pages_start\": \"3728\",\n        \"pages_end\": \"3740\",\n        \"year\": \"2001\",\n        \"synthesis_starting_materials\": \"SnI2 (Aldrich, anhydrous beads, 99.999%), anhydrous 2-butanol, 3-fluorophenethylamine (Aldrich, 99%), HI (57wt%)\",\n        \"synthesis_product\": \"dark red, thin (3- FPEA)2SnI4 crystals\",\n        \"synthesis_description\": \"In an inert environment, 1.118 g (3 mmol) of SnI2 was added to 6 mL of anhydrous 2-butanol in a test tube. Further, 0.78 mL (0.835 g; 6 mmol) of 3-fluorophenethylamine was added.The mixture was cooled to -5 \\u00b0C and 1 mL of HI was added. The mixture was heated to 94 \\u00b0C. After the complete dissolution of SnI2, the solution was cooled at 3 \\u00b0C/h to 0 \\u00b0C.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker SMART CCD diffractometer with a normal focus 2.4 kW sealed tube X-ray source (MoK\\u03b1 radiation; \\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm010105g\",\n        \"dataset_ID\": 634,\n        \"id\": 142,\n        \"compound_name\": \"4-fluoro-2-phenethylammonium tin iodide\",\n        \"formula\": \"C16H22F2N2SnI4\",\n        \"group\": \"4-fluoro-2-phenylethanaminium tetraiodostannate(II), (4-FPEA)2SnI4, (C8H11FN)2(I4Sn)\",\n        \"organic\": \"C8H11FN\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"4-fluoro-2-phenylethanaminium tin (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structurally Tailored Organic-Inorganic Perovskites: Optical Properties and Solution-Processed Channel Materials for Thin-Film Transistors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"13\",\n        \"pages_start\": \"3728\",\n        \"pages_end\": \"3740\",\n        \"year\": \"2001\",\n        \"synthesis_starting_materials\": \"SnI2 (Aldrich, anhydrous beads, 99.999%), anhydrous 2-butanol, 4-fluorophenethylamine (Aldrich, 99%), HI (57wt%)\",\n        \"synthesis_product\": \"dark red, thin (4- FPEA)2SnI4 crystals\",\n        \"synthesis_description\": \"In an inert environment, 1.118 g (3 mmol) of SnI2 was added to 10 mL of anhydrous 2-butanol in a test tube. Further, 0.79 mL (0.835 g; 6 mmol) of 4-fluorophenethylamine was added.The mixture was cooled to -5 \\u00b0C and 2 mL of HI was added. The mixture was heated to 94 \\u00b0C. After complete dissolution of SnI2, the solution was cooled at 3 \\u00b0C/h to 0 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal XRD\",\n        \"experimental_description\": \"Bruker SMART CCD diffractometer with a normal focus 2.4 kW sealed tube X-ray source (MoK\\u03b1 radiation; \\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b406671e\",\n        \"dataset_ID\": 635,\n        \"id\": 143,\n        \"compound_name\": \"1,4-phenylendiammonium copper chloride\",\n        \"formula\": \"C6H10N2CuCl4\",\n        \"group\": \"1,4-phenylendiaminium tetrachlorocuprate(II), (H2C6H4(NH2)2)CuCl4\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"1,4-phenylendiaminium copper (II) chloride\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phenylamines as building blocks to layered inorganic\\u2013organic structures\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"6\",\n        \"pages_start\": \"437\",\n        \"pages_end\": \"442\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"1,4-Phenylenediamine, ethyl ether, CuCl2, HCl\",\n        \"synthesis_product\": \"Small yellow plates\",\n        \"synthesis_description\": \"Dissolve 1,4-Phenylenediamine (18 mg, 0.17 mmol) in 2 ml of ethyl ether and layer on a solution of CuCl2 (13 mg, 0.10 mmol) dissolved in 5 mL concentrated hydrochloric acid. Allow for solvent diffusion over a period of several days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Nonius KappaCCD diffractometer using graphite-monochromated Mo K\\u03b1 radiation.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b406671e\",\n        \"dataset_ID\": 636,\n        \"id\": 144,\n        \"compound_name\": \"1,4-phenylendiammonium lead chloride\",\n        \"formula\": \"C6H10N2Pb2Cl6\",\n        \"group\": \"1,4-phenylendiaminium trichloroplumbate(II), (H2C6H4(NH2)2)(PbCl3)2\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"1,4-phenylendiaminium lead (II) chloride\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phenylamines as building blocks to layered inorganic\\u2013organic structures\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"6\",\n        \"pages_start\": \"437\",\n        \"pages_end\": \"442\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"1,4-Phenylenediamine, ethyl ether, PbCl2, HCl\",\n        \"synthesis_product\": \"Colourless plates\",\n        \"synthesis_description\": \"Dissolve 1,4-Phenylenediamine (18 mg, 0.17 mmol) in 2 ml of ethyl ether and layer on a solution of PbCl2 (31 mg, 0.11 mmol) dissolved in 5 mL concentrated hydrochloric acid. Allow crystal formation after several days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Nonius KappaCCD diffractometer using graphite-monochromated Mo K\\u03b1 radiation.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b406671e\",\n        \"dataset_ID\": 637,\n        \"id\": 145,\n        \"compound_name\": \"Bis(p-biphenylamine) copper chloride\",\n        \"formula\": \"C24H24N2CuCl4\",\n        \"group\": \"bis(1,1'biphenyl-4-aminium) tetrachlorocuprate(II), (HC6H4(NH2)(C6H5))2CuCl4\",\n        \"organic\": \"C12H12N\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"bis(1,1'biphenyl-4-aminium) copper (II) chloride\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phenylamines as building blocks to layered inorganic\\u2013organic structures\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"6\",\n        \"pages_start\": \"437\",\n        \"pages_end\": \"442\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"CuCl2, HCl, ethyl ether, p-biphenylamine\",\n        \"synthesis_product\": \"Pale yellow prisms\",\n        \"synthesis_description\": \"Dissolve CuCl2 (17 mg, 0.13 mmol) in 5 mL concentrated hydrochloric acid. Add a 2 ml ethyl ether solution of p-biphenylamine (16 mg, 0.10 mmol) as a top layer. Allow solvent diffusion over two weeks.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Nonius KappaCCD diffractometer using graphite-monochromated Mo K\\u03b1 radiation.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b406671e\",\n        \"dataset_ID\": 638,\n        \"id\": 146,\n        \"compound_name\": \"Benzidine copper chloride\",\n        \"formula\": \"C12H14N2CuCl4\",\n        \"group\": \"1,1'-biphenyl-4,4'-diaminium tetrachlorocuprate(II), (H2(C6H4)2(NH2)2)CuCl4\",\n        \"organic\": \"C12H14N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"1,1'-biphenyl-4,4'-diaminium copper (II) chloride\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phenylamines as building blocks to layered inorganic\\u2013organic structures\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"6\",\n        \"pages_start\": \"437\",\n        \"pages_end\": \"442\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"CuCl2, HCl, ethyl ether, benzidine\",\n        \"synthesis_product\": \"Pale yellow plates\",\n        \"synthesis_description\": \"Dissolve CuCl2 (25 mg, 0.19 mmol) in 8 mL concentrated hydrochloric acid. Add a 5 ml ethyl ether solution of benzidine (20 mg, 0.11 mmol) as a top layer. Allow solvent diffusion over several days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Nonius KappaCCD diffractometer using graphite-monochromated Mo K\\u03b1 radiation.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b406671e\",\n        \"dataset_ID\": 639,\n        \"id\": 147,\n        \"compound_name\": \"Bis(benzidine) lead chloride\",\n        \"formula\": \"C24H28N4PbCl6\",\n        \"group\": \"bis(1,1'-biphenyl-4,4'-diaminium) hexachloroplumbate(II), (H2(C6H4)2(NH2)2)2PbCl6\",\n        \"organic\": \"C12H14N2\",\n        \"inorganic\": \"PbCl6, Lead chloride\",\n        \"iupac\": \"bis(1,1'-biphenyl-4,4'-diaminium) lead chloride\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phenylamines as building blocks to layered inorganic\\u2013organic structures\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"6\",\n        \"pages_start\": \"437\",\n        \"pages_end\": \"442\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, ethyl ether, benzidine\",\n        \"synthesis_product\": \"Colourless needles\",\n        \"synthesis_description\": \"Dissolve PbCl2 (55 mg, 0.20 mmol) in 8 mL concentrated hydrochloric acid. Add a 5 ml ethyl ether solution of benzidine (19 mg, 0.11 mmol) as a top layer. Allow solvent diffusion over several days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Nonius KappaCCD diffractometer using graphite-monochromated Mo K\\u03b1 radiation.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01265\",\n        \"dataset_ID\": 640,\n        \"id\": 148,\n        \"compound_name\": \"bis(\\u03b2-methylphenethylammonium) lead iodide\",\n        \"formula\": \"C18H26N2PbI4\",\n        \"group\": \"bis(\\u0152\\u2264-methylphenylethanaminium) tetraiodoplumbate(II), (\\u0152\\u2264-Me-PEA)2PbI4, (C9H13N)2PbI4\",\n        \"organic\": \"C9H13N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(\\u03b2-methylphenylethanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase-Pure Hybrid Layered Lead Iodide Perovskite Films Based on a Two-Step Melt-Processing Approach\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"4267\",\n        \"pages_end\": \"4274\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\\u03b2-Methylphenethylamine, lead iodide, hydriodic acid (HI) solution (57 wt %, stabilized, 99.95%)\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"Add stoichiometric amounts of PbI2 (0.25 mmol) and \\u03b2-Me-PEA (0.5 mmol) into a 3 mL HI solution. Heat the solution to 100 \\u00b0C to dissolve all solids and then slowly cool at 2 \\u00b0C/h to room temperature. Collect crystals by filtration and wash with diethyl ether repeatedly.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"PANalytical Empyrean Powder X-ray diffractometer using Cu K\\u03b1 radiation, with the X-ray tube operating level at 45 kV and 40 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01265\",\n        \"dataset_ID\": 641,\n        \"id\": 149,\n        \"compound_name\": \"bis(\\u03b2-methylphenethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C19H32N3Pb2I7\",\n        \"group\": \"bis(\\u0152\\u2264-methylphenylethanaminium) methanaminium septaiodo diplumbate(II), (\\u0152\\u2264-Me-PEA)2MAPb2I7, (C9H13N)2CH3NH3Pb2I7\",\n        \"organic\": \"C9H13N, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(\\u03b2-methylphenylethanaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase-Pure Hybrid Layered Lead Iodide Perovskite Films Based on a Two-Step Melt-Processing Approach\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"4267\",\n        \"pages_end\": \"4274\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\\u03b2-Methylphenethylamine, methylammonium iodide, lead iodide, hydriodic acid (HI) solution (57 wt %, stabilized, 99.95%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"Add PbI2 (1 mmol), MAI (0.5 mmol), and \\u03b2-Me-PEA (0.25 mmol) into a 1.5 mL HI solution. Heat the solution to 100 \\u00b0C to dissolve all solids and then slowly cool at 2 \\u00b0C/h to room temperature. Collect crystals by filtration and wash with diethyl ether repeatedly.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"PANalytical Empyrean Powder X-ray diffractometer using Cu K\\u03b1 radiation, with the X-ray tube operating level at 45 kV and 40 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01265\",\n        \"dataset_ID\": 642,\n        \"id\": 150,\n        \"compound_name\": \"bis(\\u03b2-methylphenethylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C20H38N4Pb3I10\",\n        \"group\": \"bis(\\u0152\\u2264-methylphenylethanaminium) bis(methanaminium) decapods triplumbate(II), (\\u0152\\u2264-Me-PEA)2MA2Pb3I10, (C9H13N)2(CH3NH3)2Pb3I10\",\n        \"organic\": \"C9H13N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(\\u03b2-methylphenylethanaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase-Pure Hybrid Layered Lead Iodide Perovskite Films Based on a Two-Step Melt-Processing Approach\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"4267\",\n        \"pages_end\": \"4274\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\\u03b2-Methylphenethylamine, methylammonium iodide, lead iodide, hydriodic acid (HI) solution (57 wt %, stabilized, 99.95%)\",\n        \"synthesis_product\": \"Deep brown crystals\",\n        \"synthesis_description\": \"Add PbI2 (1 mmol), MAI (0.667 mmol), and \\u03b2-Me-PEA (0.065 mmol) into a 1.5 mL HI solution. Heat the solution to 100 \\u00b0C to dissolve all solids and then slowly cool at 2 \\u00b0C/h to room temperature. Collect crystals by filtration and wash with diethyl ether repeatedly.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"PANalytical Empyrean Powder X-ray diffractometer using Cu K\\u03b1 radiation, with the X-ray tube operating level at 45 kV and 40 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic034235y\",\n        \"dataset_ID\": 643,\n        \"id\": 151,\n        \"compound_name\": \"5,5\\u2018-bis(ammoniumethylsulfanyl)-2,2\\u2018-bithiophene lead iodide\",\n        \"formula\": \"C12H18N2S4PbI4\",\n        \"group\": \"(2,2'-(thioethanaminium)-5,5'-bithiophene) tetraiodoplumbate(II), (BAESBT)PbI4\",\n        \"organic\": \"C6H9I2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"(2,2'-(thioethanaminium)-5,5'-bithiophene) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of Mono- versus Di-ammonium Cation of 2,2\\u2018-Bithiophene Derivatives on the Structure of Organic\\u2212Inorganic Hybrid Materials Based on Iodo Metallates\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"5330\",\n        \"pages_end\": \"5339\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"(BAESBT)Cl2 , PbI2, KI, HI\",\n        \"synthesis_product\": \"Orange plate single crystals\",\n        \"synthesis_description\": \"First prepare (BAESBT)Cl2 Salt (refer to the experimental section). Mix (BAESBT)Cl2 (12.8 mg, 0.03 mmol), PbI2 (15 mg, 0.033 mmol), excess KI (7 g), one drop of concentrated HI, and H2O (10 mL) in a sealed Pyrex tube. Keep the temperature at 90 \\u00b0C for 1 h and then at 110 \\u00b0C for 4 h. Subsequently, cool to room temperature at 2 \\u00b0C/h resulting in well-formed orange plate single crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius MACH3 four-circle diffractometer with graphite monochromated, Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic034235y\",\n        \"dataset_ID\": 644,\n        \"id\": 152,\n        \"compound_name\": \"Tetrakis(5-ammoniumethylsulfanyl-2,2\\u2018-bithiophene) lead iodide\",\n        \"formula\": \"C40H48N4S12Pb3I10\",\n        \"group\": \"(AESBT)4Pb3I10, tetrakis(2,2'-(thioethanaminium)-5,5'-bithiophene) decaiodo triplumbate(II)\",\n        \"organic\": \"C10H12NS3\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"tetrakis(2,2'-(thioethanaminium)-5,5'-bithiophene) lead iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of Mono- versus Di-ammonium Cation of 2,2\\u2018-Bithiophene Derivatives on the Structure of Organic\\u2212Inorganic Hybrid Materials Based on Iodo Metallates\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"5330\",\n        \"pages_end\": \"5339\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"(AESBT)Cl, PbI2, HI\",\n        \"synthesis_product\": \"Yellow needle single crystals\",\n        \"synthesis_description\": \"First prepare (AESBT)Cl Salt (refer to the experimental section). Mix (AESBT)Cl (9.7 mg, 0.037 mmol), PbI2 (12.8 mg, 0.028 mmol), three drops of concentrated HI, and H2O (4 mL) in a sealed Pyrex tube. Keep the temperature at 100 \\u00b0C for 4 h and then cool to room temperature at 2 \\u00b0C/h affording well-formed yellow needle single crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Enraf-Nonius MACH3 four-circle diffractometer with graphite monochromated, Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic034235y\",\n        \"dataset_ID\": 645,\n        \"id\": 153,\n        \"compound_name\": \"Tris(5-ammoniumethylsulfanyl-2,2\\u2018-bithiophene) bismuth iodide\",\n        \"formula\": \"C30H36N3S9Bi2I9\",\n        \"group\": \"(AESBT)3Bi2I9, tris(2,2'-(thioethanaminium)-5,5'-bithiophene) nonaiodo dibismuthate(II)\",\n        \"organic\": \"C10H12NS3\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"tris(2,2'-(thioethanaminium)-5,5'-bithiophene) lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of Mono- versus Di-ammonium Cation of 2,2\\u2018-Bithiophene Derivatives on the Structure of Organic\\u2212Inorganic Hybrid Materials Based on Iodo Metallates\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"5330\",\n        \"pages_end\": \"5339\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"(AESBT)Cl, BiCl3, KI, HI\",\n        \"synthesis_product\": \"Red plate single crystals\",\n        \"synthesis_description\": \"First prepare (AESBT)Cl Salt (refer to the experimental section). Mix (AESBT)Cl (16.7 mg, 0.06 mmol), BiCl3 (18.5 mg, 0.028 mmol), excess KI (1 g), two drops of concentrated HI and H2O (5 mL) in a sealed Pyrex tube. Keep the temperature at 100 \\u00b0C for 10 h and then cool to room temperature at 2 \\u00b0C/h leading to well-formed red plate single crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE-IPDS diffractometer with graphite monochromated, Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b02682\",\n        \"dataset_ID\": 646,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Cs2InAgCl6: A New Lead-Free Halide Double Perovskite with Direct Band Gap\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"772\",\n        \"pages_end\": \"778\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Indium chloride (InCl3, Sigma-Aldrich, 99.99%), Silver chloride (AgCl, Sigma-Aldrich, 99%), HCl, Cesium chloride (CsCl, Sigma-Aldrich, 99.9%)\",\n        \"synthesis_product\": \"White powder\",\n        \"synthesis_description\": \"Mix 1 mmol InCl3 and AgCl in 5 mL 10 M HCl. Add 2 mmol of CsCl and heat the solution to 115 \\u00b0C. Leave the hot solution for 30 min under gentle stirring to ensure a complete reaction before filtering. Wash the resulting solid with ethanol and dry in a furnace overnight at 100 \\u00b0C.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Panalytical X\\u2019pert diffractometer (Cu\\u2212K\\u03b11 radiation; \\u03bb = 154.05 pm) at room temperature. Structural parameters were obtained by Rietveld refinement.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b02682\",\n        \"dataset_ID\": 647,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"LDA\",\n        \"k_point_grid\": \"Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density\",\n        \"numerical_accuracy\": \"10\\u22123 Ry threshold for convergence of forces; 10\\u22124 Ry threshold for total energy\",\n        \"title\": \"Cs2InAgCl6: A New Lead-Free Halide Double Perovskite with Direct Band Gap\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"772\",\n        \"pages_end\": \"778\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b02682\",\n        \"dataset_ID\": 648,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density\",\n        \"numerical_accuracy\": \"10\\u22123 Ry threshold for convergence of forces; 10\\u22124 Ry threshold for total energy\",\n        \"title\": \"Cs2InAgCl6: A New Lead-Free Halide Double Perovskite with Direct Band Gap\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"772\",\n        \"pages_end\": \"778\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b02682\",\n        \"dataset_ID\": 649,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE\",\n        \"k_point_grid\": \"Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density\",\n        \"numerical_accuracy\": \"10\\u22123 Ry threshold for convergence of forces; 10\\u22124 Ry threshold for total energy\",\n        \"title\": \"Cs2InAgCl6: A New Lead-Free Halide Double Perovskite with Direct Band Gap\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"772\",\n        \"pages_end\": \"778\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b02682\",\n        \"dataset_ID\": 650,\n        \"id\": 155,\n        \"compound_name\": \"Cesium silver indium bromide\",\n        \"formula\": \"Cs2InAgBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromoindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-23\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"LDA\",\n        \"k_point_grid\": \"Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density\",\n        \"numerical_accuracy\": \"10\\u22123 Ry threshold for convergence of forces; 10\\u22124 Ry threshold for total energy\",\n        \"title\": \"Cs2InAgCl6: A New Lead-Free Halide Double Perovskite with Direct Band Gap\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"772\",\n        \"pages_end\": \"778\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.6b02682\",\n        \"dataset_ID\": 651,\n        \"id\": 156,\n        \"compound_name\": \"Cesium silver indium iodide\",\n        \"formula\": \"Cs2InAgI6\",\n        \"group\": \"Dicesium triiodoargentate(I) triiodoindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgI6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-23\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"Quantum ESPRESSO\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"LDA\",\n        \"k_point_grid\": \"Brillouin zone was sampled using a 15 X 15 X 15 unshifted grid\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Ultrasoft pseudopotentials; Planewaves energy cutoffs 35 Ry for electronic wave functions; 280 Ry for charge density\",\n        \"numerical_accuracy\": \"10\\u22123 Ry threshold for convergence of forces; 10\\u22124 Ry threshold for total energy\",\n        \"title\": \"Cs2InAgCl6: A New Lead-Free Halide Double Perovskite with Direct Band Gap\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"772\",\n        \"pages_end\": \"778\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.6b03207\",\n        \"dataset_ID\": 652,\n        \"id\": 157,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"Cs2SnI6\",\n        \"group\": \"Dicesium hexastannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-23\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect Tolerance to Intolerance in the Vacancy-Ordered Double Perovskite Semiconductors Cs2SnI6 and Cs2TeI6\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"8453\",\n        \"pages_end\": \"8464\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), SnI4\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"In a beaker, slowly add \\u223c0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve SnI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the SnI4 precursors gently to T \\u2248 60 \\u00b0C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the SnI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 \\u00b0C for 24 h.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"POWGEN diffractometer at the Spallation Neutron Source, Oak Ridge National Laboratory; Rietveld analysis\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.6b03207\",\n        \"dataset_ID\": 653,\n        \"id\": 158,\n        \"compound_name\": \"Cesium tellurium iodide\",\n        \"formula\": \"Cs2TeI6\",\n        \"group\": \"Dicesium hexatellurate(II), Cs2TeI6\",\n        \"organic\": \"None\",\n        \"inorganic\": \"TeI6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect Tolerance to Intolerance in the Vacancy-Ordered Double Perovskite Semiconductors Cs2SnI6 and Cs2TeI6\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"8453\",\n        \"pages_end\": \"8464\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), TeI4\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"In a beaker, slowly add \\u223c0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve TeI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the TeI4 precursors gently to T \\u2248 60 \\u00b0C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the TeI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 \\u00b0C for 24 h.\",\n        \"experimental_method\": \"Powder neutron diffraction\",\n        \"experimental_description\": \"POWGEN diffractometer at the Spallation Neutron Source, Oak Ridge National Laboratory; Rietveld analysis\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c0dt01805h\",\n        \"dataset_ID\": 655,\n        \"id\": 159,\n        \"compound_name\": \"Bis(nonylammonium) lead ioide\",\n        \"formula\": \"C18H44N2PbI4\",\n        \"group\": \"bis(Nonylammonium)tetraiodoplumbate(II), (C9H19NH3)2PbI4\",\n        \"organic\": \"C9H22N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(nonane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, characterization and phase transitions of the inorganic\\u2013organic layered perovskite-type hybrids [(CnH2n+1NH3)2PbI4], n = 7, 8, 9 and 10\",\n        \"journal\": \"Dalton Transactions\",\n        \"vol\": \"41\",\n        \"pages_start\": \"1146\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"PbI2, HI (47% in water), C9H19NH2\",\n        \"synthesis_product\": \"Orange plate-like crystal\",\n        \"synthesis_description\": \"0.024 g PbI2 (0.052 mmol) was dissolved in 7 ml HI. 0.015 g C9H19NH2 (0.105 mmol) was added to it. The formed precipitate was dissolved by refluxing for 2 h at 90 degrees C. The solution was slowly cooled at 2 degrees C/hr to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker Apex II CCD diffractometer11 with graphite-monochromated Mo-K\\u03b11 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"223.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6mh00053c\",\n        \"dataset_ID\": 656,\n        \"id\": 160,\n        \"compound_name\": \"Bis(methylammonium) potassium bismuth chloride\",\n        \"formula\": \"C2H12N2KBiCl6\",\n        \"group\": \"bis(methanaminium) potassium hexachlorobismuthate(II), (MA)2KBiCl6, methylammonium potassium bismuth chloride, (CH3NH3)2KBiCl6\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"KBiCl6, Potassium bismuth chloride\",\n        \"iupac\": \"bis(methanaminium) potassium bismuth chloride\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"The synthesis, structure and electronic properties of a lead-free hybrid inorganic\\u2013organic double perovskite (MA)2KBiCl6 (MA = methylammonium)\",\n        \"journal\": \"Materials Horizon\",\n        \"vol\": \"3\",\n        \"pages_start\": \"328\",\n        \"pages_end\": \"332\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium chloride (synthesized from methylamine solution (40 wt% in H2O) and HCl (37% in H2O)), HCl, BiCl3, K\",\n        \"synthesis_product\": \"Colorless prismatic crystals\",\n        \"synthesis_description\": \"2.4 mmol CH3NH3Cl, 1.2 mmol KCl, and 1.2 mmol BiCl3 in 1 ml HCl acid solution were loaded in a stainless steel Parr autoclave. The hydrothermal reaction was performed at 423 K.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected in an Oxford Gemini E Ultra diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073\\u00c5), equipped with an Eos CCD detector.\",\n        \"physical_property\": \"297.8 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 657,\n        \"id\": 161,\n        \"compound_name\": \"butylammonium tin iodide\",\n        \"formula\": \"C8H22N2SnI6\",\n        \"group\": \"bis(butane-1-aminium) hexaiodostannate(II), BA2SnI4\",\n        \"organic\": \"C4H11N\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tin iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, Ethanol, SnI2, butylammonium iodide (BAI)\",\n        \"synthesis_product\": \"dark purple plate-like crystals\",\n        \"synthesis_description\": \"In an inert atmosphere,  stoichiometric quantities of BAI and SnI2 were added to HI. The solution was heated to 75\\u00b0C to dissolve the solids and subsequently cooled to 5 \\u00b0C at a rate of 1.5 \\u00b0C/hour.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb =  0.71069 \\u00c5).\",\n        \"physical_property\": \"273.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic500554z\",\n        \"dataset_ID\": 658,\n        \"id\": 162,\n        \"compound_name\": \"Tetrakis(pentylammonium) cadmium chloride\",\n        \"formula\": \"C20H48N4Cd3Cl10\",\n        \"group\": \"[C5H9NH3]4Cd3Cl10, tetrakis(pentane-1-aminium) decachloro tricadmate(II)\",\n        \"organic\": \"C5H12N\",\n        \"inorganic\": \"Cd3Cl10, Cadmium chloride\",\n        \"iupac\": \"tetetrakis(pentane-1-aminium) cadmium chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Phase Transitions of a Layered Organic\\u2212Inorganic Hybrid Compound: Tetra(cyclopentylammonium) Decachlorotricadmate(II), [C5H9NH3]4Cd3Cl10\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"53\",\n        \"pages_start\": \"8913\",\n        \"pages_end\": \"8918\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"Concentrated HCl, Cyclopentamine, Cadmium Chloride (CdCl2)\",\n        \"synthesis_product\": \"Colorless block-shaped crystals\",\n        \"synthesis_description\": \"Cyclopentylamine (1.70 g, 0.02 mol) was taken in water (30 mL). Concentrated HCl (4.00 g, 0.04 mol) was added dropwise to it. The obtained solution mixture was added to an aqueous solution of CdCl2 (3.42 g, 0.015 mol). Slow evaporation of the solution at room temperature forms the crystals.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected on a Rigaku Saturn 924 diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic048814u\",\n        \"dataset_ID\": 659,\n        \"id\": 164,\n        \"compound_name\": \"2-hydroxyethylammonium lead iodide\",\n        \"formula\": \"C4H16N2O2PbI4\",\n        \"group\": \"bis(2-hydroxyethanaminium) tetraiodoplumbate(II), (HO(CH2)2NH3)2PbI4\",\n        \"organic\": \"C2H8NO\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-hydroxyethanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Unique Hydrogen Bonding Correlating with a Reduced Band Gap and Phase Transition in the Hybrid Perovskites (HO(CH2)2NH3)2PbX4 (X ) I, Br)\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"43\",\n        \"pages_start\": \"8361\",\n        \"pages_end\": \"8366\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"ethanolamine (NH2(CH2)2OH), lead iodide (PbI2), Conc. HI, Acetonitrile (CH3CN)\",\n        \"synthesis_product\": \"Orange needle-like crystal\",\n        \"synthesis_description\": \"NH2(CH2)2OH (111 mg, 1.82 mmol), PbI2 (420 mg, 0.91 mmol), a few drops of concentrated HI, and acetonitrile (20 mL) was stirred a few minutes at room temperature. Evaporating the solution at 20 \\u00b0C by stirring formed the crystals. The crystals were filtered and washed with cold acetonitrile.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected on an Enraf-Nonius MACH3 four-circle diffractometer using graphite-monochromated Mo K\\u03b1 radiation (\\u03bb= 0.710 73 \\u00c5).\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic048814u\",\n        \"dataset_ID\": 660,\n        \"id\": 164,\n        \"compound_name\": \"2-hydroxyethylammonium lead iodide\",\n        \"formula\": \"C4H16N2O2PbI4\",\n        \"group\": \"bis(2-hydroxyethanaminium) tetraiodoplumbate(II), (HO(CH2)2NH3)2PbI4\",\n        \"organic\": \"C2H8NO\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-hydroxyethanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Unique Hydrogen Bonding Correlating with a Reduced Band Gap and Phase Transition in the Hybrid Perovskites (HO(CH2)2NH3)2PbX4 (X ) I, Br)\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"43\",\n        \"pages_start\": \"8361\",\n        \"pages_end\": \"8366\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"ethanolamine (NH2(CH2)2OH), lead iodide (PbI2), Conc. HI, Acetonitrile (CH3CN)\",\n        \"synthesis_product\": \"(HO(CH2)2NH3)2PbI4 film\",\n        \"synthesis_description\": \"NH2(CH2)2OH (111 mg, 1.82 mmol), PbI2 (420 mg, 0.91 mmol), a few drops of concentrated HI, and acetonitrile (20 mL) was stirred a few minutes at room temperature. Evaporating the solution at 20 \\u00b0C by stirring formed the crystals. The crystals were filtered and washed with cold acetonitrile.\\r\\nThe crystals were further dissolved in acetonitrile and spin-coated to form the films.\",\n        \"experimental_method\": \"UV-visible absorption\",\n        \"experimental_description\": \"Spectra were recorded using a Lambda 19 Perkin-Elmer spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B205543K\",\n        \"dataset_ID\": 661,\n        \"id\": 165,\n        \"compound_name\": \"Bis(2-thienylmethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C11H22N3SPb2I7\",\n        \"group\": \"(C4H3SCH2NH3)2(CH3NH3)Pb2I7, bis(2-thienylmethanaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C5H8NS, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(2-thienylmethanaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"(C4H3SCH2NH3)2(CH3NH3)Pb2I7 : non-centrosymmetrical crystal structure of a bilayer hybrid perovskite\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"18\",\n        \"pages_start\": \"2160\",\n        \"pages_end\": \"2161\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"C4H3SCH2NH2, HI, PbI2\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Under an argon atmosphere, stoichiometric quantities of PbI2 (0.4 mmol) and C4H3SCH2NH2 were mixed in a concentrated HI solution (8 mL) by heating at 60 \\u00b0C. Slow cooling of the solution, forms the crystals.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an Enraf Nonius CAD4 diffractometer and using Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aba2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B205543K\",\n        \"dataset_ID\": 662,\n        \"id\": 165,\n        \"compound_name\": \"Bis(2-thienylmethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C11H22N3SPb2I7\",\n        \"group\": \"(C4H3SCH2NH3)2(CH3NH3)Pb2I7, bis(2-thienylmethanaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C5H8NS, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(2-thienylmethanaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"(C4H3SCH2NH3)2(CH3NH3)Pb2I7 : non-centrosymmetrical crystal structure of a bilayer hybrid perovskite\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"18\",\n        \"pages_start\": \"2160\",\n        \"pages_end\": \"2161\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"C4H3SCH2NH2, HI, PbI2\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Under an argon atmosphere, stoichiometric quantities of PbI2 (0.4 mmol) and C4H3SCH2NH2 were mixed in a concentrated HI solution (8 mL) by heating at 60 \\u00b0C. Slow cooling of the solution, formed the crystals.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aba2\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja500618z\",\n        \"dataset_ID\": 663,\n        \"id\": 166,\n        \"compound_name\": \"Guanidinium manganese formate\",\n        \"formula\": \"CH6N3MnC3HHO6\",\n        \"group\": \"[C(NH2)3][Mn(HCOO)3]\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"[Mn(HCOO)3]-, Manganese formate\",\n        \"iupac\": \"Guanidinium manganese formate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"organic bridged 0D Perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Mechanical Tunability via Hydrogen Bonding in Metal\\u2212Organic Frameworks with the Perovskite Architecture\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"136\",\n        \"pages_start\": \"7801\",\n        \"pages_end\": \"7804\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an Oxford Diffraction Gemini E Ultra diffractometer using Mo radiation ( \\u03bb=0.71073 \\u00c5, operating at 50 kV and 40 mA).\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja500618z\",\n        \"dataset_ID\": 664,\n        \"id\": 167,\n        \"compound_name\": \"Azetidium manganese formate\",\n        \"formula\": \"C3H8NMnC3H3O6\",\n        \"group\": \"[(CH2)3NH2][Mn(HCOO)3]\",\n        \"organic\": \"C3H8N\",\n        \"inorganic\": \"[Mn(HCOO)3]-, Manganese formate\",\n        \"iupac\": \"azetidin-1-ium manganese formate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"organic bridged 3D Perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Mechanical Tunability via Hydrogen Bonding in Metal\\u2212Organic Frameworks with the Perovskite Architecture\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"136\",\n        \"pages_start\": \"7801\",\n        \"pages_end\": \"7804\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an Oxford Diffraction Gemini E Ultra diffractometer using Mo radiation ( \\u03bb=0.71073 \\u00c5, operating at 50 kV and 40 mA).\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.7b03229\",\n        \"dataset_ID\": 665,\n        \"id\": 168,\n        \"compound_name\": \"Guanidinium zinc fomate\",\n        \"formula\": \"CH6N3ZnC3HHO6\",\n        \"group\": \"[Gua][Zn(HCOO)3], [C(NH2)3][Zn(HCOO)3]\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"[Zn(HCOO)3]-, Zinc formate\",\n        \"iupac\": \"Guanidinium zinc fomate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"organic bridged 3D Perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Jahn\\u2212Teller Effect on Framework Flexibility of Hybrid Organic\\u2212 Inorganic Perovskites\",\n        \"journal\": \"the Journal of Physical Chemistry Letters\",\n        \"vol\": \"9\",\n        \"pages_start\": \"751\",\n        \"pages_end\": \"755\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an Oxford Gemini single-crystal diffractometer using Mo radiation (\\u03bb = 0.71073 \\u00c5, operating at 50 kV and 40 mA)\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.7b03229\",\n        \"dataset_ID\": 666,\n        \"id\": 169,\n        \"compound_name\": \"Guanidinium copper fomate\",\n        \"formula\": \"CH6N3CuC3HHO6\",\n        \"group\": \"[Gua][Cu(HCOO)3], [C(NH2)3][Cu(HCOO)3]\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"[Cu(HCOO)3]-, Copper formate\",\n        \"iupac\": \"Guanidinium copper fomate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"organic bridged 3D Perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Jahn\\u2212Teller Effect on Framework Flexibility of Hybrid Organic\\u2212 Inorganic Perovskites\",\n        \"journal\": \"the Journal of Physical Chemistry Letters\",\n        \"vol\": \"9\",\n        \"pages_start\": \"751\",\n        \"pages_end\": \"755\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an Oxford Gemini single-crystal diffractometer using Mo radiation (\\u03bb = 0.71073 \\u00c5, operating at 50 kV and 40 mA).\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0521527\",\n        \"dataset_ID\": 667,\n        \"id\": 170,\n        \"compound_name\": \"dimethylammonium iron azido formate\",\n        \"formula\": \"[(CH3)2NH2][Fe(N3)2(HCOO)]\",\n        \"group\": \"[Fe(N3)2(HCOO)][(CH3)2NH2]\",\n        \"organic\": \"C2NH8\",\n        \"inorganic\": \"[Fe(N3)2(HCOO)]-\",\n        \"iupac\": \"dimethylammonium iron azido formate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"[N3-] bridged 1D structure\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two Chain Compounds of [M(N3)2(HCOO)][(CH3)2NH2] (M ) Fe and Co) with a Mixed Azido/Formato Bridge Displaying Metamagnetic Behavior\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"2782\",\n        \"pages_end\": \"2784\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"formic acid, NaN3, dimethylamine, Fe(ClO4)2\\u201a4H2O, methanol\",\n        \"synthesis_product\": \"Column shaped yellow-green crystals\",\n        \"synthesis_description\": \"In a methanol solution containing formic acid, NaN3, and dimethylamine, another methanol solution of Fe(ClO4)2\\u201a4H2O was diffused.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using a NONIUS KappaCCD Diffractometer with Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0521527\",\n        \"dataset_ID\": 668,\n        \"id\": 171,\n        \"compound_name\": \"dimethylammonium cobalt azido formate\",\n        \"formula\": \"[(CH3)2NH2][Co(N3)2(HCOO)]\",\n        \"group\": \"[Co(N3)2(HCOO)][(CH3)2NH2]\",\n        \"organic\": \"C2NH8\",\n        \"inorganic\": \"[Co(N3)2(HCOO)]-\",\n        \"iupac\": \"dimethylammonium cobalt azido formate\",\n        \"last_update\": \"2019-09-10\",\n        \"description\": \"[N3-] bridged 1D structure\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two Chain Compounds of [M(N3)2(HCOO)][(CH3)2NH2] (M ) Fe and Co) with a Mixed Azido/Formato Bridge Displaying Metamagnetic Behavior\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"2782\",\n        \"pages_end\": \"2784\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"formic acid, NaN3, dimethylamine, CoCl2\\u201a6H2O, methanol\",\n        \"synthesis_product\": \"Column shaped pink crystals\",\n        \"synthesis_description\": \"In a methanol solution containing formic acid, NaN3, and dimethylamine, another methanol solution of CoCl2\\u201a6H2O was diffused.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using a NONIUS KappaCCD Diffractometer with Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic700924j\",\n        \"dataset_ID\": 669,\n        \"id\": 172,\n        \"compound_name\": \"N,N\\u2018-dimethylethylenediammonium manganese formate\",\n        \"formula\": \"C4H14N2Mn2C6H6O12\",\n        \"group\": \"[CH3NH2(CH2)2NH2CH3][Mn2(HCOO)6]\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"[Mn2(HCOO)6]2-, Manganese formate\",\n        \"iupac\": \"bis(N,N'-dimethylethane-1,2-diaminium) manganese formate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[CH3NH2(CH2)2NH2CH3][M2(HCOO)6] (M = Mn(II) and Co(II)): Weak Ferromagnetic Metal Formate Frameworks of Unique Binodal 6-Connected (4^12\\u201a6^3)(4^9\\u201a6^6) Topology, Templated by a Diammonium Cation\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"46\",\n        \"pages_start\": \"8439\",\n        \"pages_end\": \"8441\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"N,N\\u2032-dimethylethylenediamine (dmen), formic acid (HCOOH), methanol, Mn(ClO4)2\\u201a6H2O\",\n        \"synthesis_product\": \"Colorless needle-like crystals\",\n        \"synthesis_description\": \"0.35 g of dmen and 0.40 g of HCOOH were mixed in 10 mL of methanol. 2 mL of this solution was mixed with 2.0 mL of a 0.20 M methanol solution of Mn(ClO4)2\\u201a6H2O.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected on a Nonius Kappa CCD diffractometer using graphite-monochromated Mo K\\u03b1 (\\u03bb = 0.710 73 \\u00c5) radiation.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"P-31c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic700924j\",\n        \"dataset_ID\": 670,\n        \"id\": 173,\n        \"compound_name\": \"N,N\\u2018-dimethylethylenediammonium copper formate\",\n        \"formula\": \"C4H14N2Cu2C6H6O12\",\n        \"group\": \"[CH3NH2(CH2)2NH2CH3][Cu2(HCOO)6]\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"[Co2(HCOO)6]2-, Copper formate\",\n        \"iupac\": \"bis(N,N'-dimethylethane-1,2-diaminium) copper formate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[CH3NH2(CH2)2NH2CH3][M2(HCOO)6] (M = Mn(II) and Co(II)): Weak Ferromagnetic Metal Formate Frameworks of Unique Binodal 6-Connected (4^12\\u201a6^3)(4^9\\u201a6^6) Topology, Templated by a Diammonium Cation\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"46\",\n        \"pages_start\": \"8439\",\n        \"pages_end\": \"8441\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"N,N\\u2032-dimethylethylenediamine (dmen), formic acid (HCOOH), methanol, Co(ClO4)2\\u201a6H2O\",\n        \"synthesis_product\": \"Red block-like crystals\",\n        \"synthesis_description\": \"0.35 g of dmen and 0.40 g of HCOOH were mixed in 10 mL of methanol. 2 mL of this solution was mixed with 2.0 mL of a 0.20 M methanol solution of Co(ClO4)2\\u201a6H2O.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected on a Nonius Kappa CCD diffractometer using graphite-monochromated Mo K\\u03b1 (\\u03bb = 0.710 73 \\u00c5) radiation.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"P-31c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0498081\",\n        \"dataset_ID\": 671,\n        \"id\": 174,\n        \"compound_name\": \"dimethylamine manganese formate\",\n        \"formula\": \"C2H8NMnC3H3O6\",\n        \"group\": \"Mn(CHOO)3[NH2(CH3)2], [(CH3)2NH2][Mn(CHOO)3]\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"[Mn(CHOO)3]-, Manganese formate\",\n        \"iupac\": \"N,N-dimethanaminium manganese formate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Perovskite-like Metal Formates with Weak Ferromagnetism and as Precursors to Amorphous Materials\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"43\",\n        \"pages_start\": \"4615\",\n        \"pages_end\": \"4625\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"MnCl2\\u00b74H2O, dimethylformamide (DMF),\",\n        \"synthesis_product\": \"Colorless block-like crystals\",\n        \"synthesis_description\": \"MnCl2\\u00b74H2O(1 mmol), DMF (6 mL), and H2O (6 mL) were heated in a Teflon-lined autoclave at 140 \\u00b0C for 3 days. The solution was slowly cooled and the residual solution was evaporated at room temperature for about 1 week.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using Rigaku R-Axis RIPID IP with Mo\\u2212K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) at 293 K.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0498081\",\n        \"dataset_ID\": 672,\n        \"id\": 175,\n        \"compound_name\": \"dimethylamine cobalt formate\",\n        \"formula\": \"C2H8NCoC3H3O6\",\n        \"group\": \"Co(CHOO)3[NH2(CH3)2], [(CH3)2NH2][Co(CHOO)3]\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"[Co(CHOO)3]-, Cobalt formate\",\n        \"iupac\": \"N,N-dimethanaminium cobalt formate\",\n        \"last_update\": \"2022-06-08\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Perovskite-like Metal Formates with Weak Ferromagnetism and as Precursors to Amorphous Materials\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"43\",\n        \"pages_start\": \"4615\",\n        \"pages_end\": \"4625\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"CoCl2\\u00b76H2O, dimethylformamide (DMF),\",\n        \"synthesis_product\": \"Pink block-like crystals\",\n        \"synthesis_description\": \"CoCl2\\u00b76H2O (1 mmol), DMF (6 mL), and H2O (6 mL) were heated in a Teflon-lined autoclave at 140 \\u00b0C for 3 days. The solution was slowly cooled and the residual solution was evaporated at room temperature for about 1 week.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using Rigaku R-Axis RIPID IP with Mo\\u2212K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) at 293 K.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"R-3c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0498081\",\n        \"dataset_ID\": 673,\n        \"id\": 176,\n        \"compound_name\": \"dimethylamine nickle formate\",\n        \"formula\": \"C2H8NNiC3H3O6\",\n        \"group\": \"Ni(CHOO)3[NH2(CH3)2], [(CH3)2NH2][Ni(CHOO)3]\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"[Ni(CHOO)3]-, Nickle formate\",\n        \"iupac\": \"N,N-dimethanaminium nickle formate\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Perovskite-like Metal Formates with Weak Ferromagnetism and as Precursors to Amorphous Materials\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"43\",\n        \"pages_start\": \"4615\",\n        \"pages_end\": \"4625\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"NiCl2\\u00b76H2O, dimethylformamide (DMF),\",\n        \"synthesis_product\": \"Blue block-like crystals\",\n        \"synthesis_description\": \"NiCl2\\u00b76H2O (1 mmol), DMF (6 mL), and H2O (6 mL) were heated in a Teflon-lined autoclave at 140 \\u00b0C for 3 days. The solution was slowly cooled and the residual solution was evaporated at room temperature for about 1 week.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using Rigaku R-Axis RIPID IP with Mo\\u2212K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) at 293 K.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6ta05055g\",\n        \"dataset_ID\": 680,\n        \"id\": 177,\n        \"compound_name\": \"1,8-octyldiammonium lead iodide\",\n        \"formula\": \"C8H22N2PbI4\",\n        \"group\": \"OdAPbI4, [NH3(CH2)8NH3]PbI4, octane-1,8-diaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H22N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"octane-1,8-diaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered 2D alkyldiammonium lead iodide perovskites: synthesis, characterization, and use in solar cells\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"4\",\n        \"pages_start\": \"15638\",\n        \"pages_end\": \"15646\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"1,8-diaminooctane (98%),  hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%)\",\n        \"synthesis_product\": \"block-like crystals\",\n        \"synthesis_description\": \"1 mol 1,8-diaminooctane (98%) was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether .\\r\\n\\r\\nPbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to  \\u221210 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal X-ray crystallography\",\n        \"experimental_description\": \"Data were collected using a Bruker APEXII diffractometer (MoK\\u03b1 radiation), equipped with a CCD detector.\",\n        \"physical_property\": \"200.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6ta05055g\",\n        \"dataset_ID\": 681,\n        \"id\": 177,\n        \"compound_name\": \"1,8-octyldiammonium lead iodide\",\n        \"formula\": \"C8H22N2PbI4\",\n        \"group\": \"OdAPbI4, [NH3(CH2)8NH3]PbI4, octane-1,8-diaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H22N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"octane-1,8-diaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered 2D alkyldiammonium lead iodide perovskites: synthesis, characterization, and use in solar cells\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"4\",\n        \"pages_start\": \"15638\",\n        \"pages_end\": \"15646\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"1,8-diaminooctane (98%), hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%), TiO2\",\n        \"synthesis_product\": \"yellow film\",\n        \"synthesis_description\": \"1 mol 1,8-diaminooctane (98%) was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether . PbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to \\u221210 \\u00b0C.\\r\\n1:3.5 ratio of TiO2 Dyesol paste and ethanol (99.5%) produced a \\u223c250 nm mesoporous film on a microscopic slide. The film was sintered and was used as a substrate. DMF solution of the perovskite crystal was spin-coated and the film was heated at 90 \\u00b0C for 10 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Spectra were recorded using UV-visible Cary 300 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6ta05055g\",\n        \"dataset_ID\": 682,\n        \"id\": 178,\n        \"compound_name\": \"1,6-diaminohexane lead iodide\",\n        \"formula\": \"C6H18N2PbI4\",\n        \"group\": \"HdAPbI4, hexane-1,6-diaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"hexane-1,6-diaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered 2D alkyldiammonium lead iodide perovskites: synthesis, characterization, and use in solar cells\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"4\",\n        \"pages_start\": \"15638\",\n        \"pages_end\": \"15646\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"1,6-diaminohexane (98%), hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%)\",\n        \"synthesis_product\": \"block-like crystals\",\n        \"synthesis_description\": \"1 mol 1,6-diaminohexane was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether. PbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to \\u221210 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal X-ray crystallography\",\n        \"experimental_description\": \"Data were collected using a Bruker APEXII diffractometer (MoK\\u03b1 radiation), equipped with a CCD detector.\",\n        \"physical_property\": \"200.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6ta05055g\",\n        \"dataset_ID\": 683,\n        \"id\": 178,\n        \"compound_name\": \"1,6-diaminohexane lead iodide\",\n        \"formula\": \"C6H18N2PbI4\",\n        \"group\": \"HdAPbI4, hexane-1,6-diaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"hexane-1,6-diaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered 2D alkyldiammonium lead iodide perovskites: synthesis, characterization, and use in solar cells\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"4\",\n        \"pages_start\": \"15638\",\n        \"pages_end\": \"15646\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"1,6-diaminohexane (98%), hydriodic acid (HI, 57% w/w in water and stabilized with 1.5% hypophosphorous acid), lead iodide (PbI2, 99.999%), TiO2\",\n        \"synthesis_product\": \"yellow film\",\n        \"synthesis_description\": \"1 mol 1,6-diaminohexane (98%) was mixed with 2 mol equivalents of HI and was stirred for 2 hours in an ice bath. The resulting salt was recovered by evaporation of the solvent and washing with diethyl ether . PbI2 (2 mol equivalents) was dissolved in 4 mL HI. Diammonium iodide salt (1 mol equivalent) was dissolved in 3 mL HI. The two solutions were mixed and stirred at 90 degrees C for 1 hour and half of the solvent was evaporated. The stirring was stopped and the temperature was gradually decreased (5 degrees C/hour) to \\u221210 \\u00b0C. 1:3.5 ratio of TiO2 Dyesol paste and ethanol (99.5%) produced a \\u223c250 nm mesoporous film on a microscopic slide. The film was sintered and was used as a substrate. DMF solution of the perovskite crystal was spin-coated and the film was heated at 90 \\u00b0C for 10 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Spectra were recorded using UV-visible Cary 300 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1515/znb-1993-0727\",\n        \"dataset_ID\": 685,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Preparation and Characterization of (C6H5CH2CH2NH3)2SnI4 and (C6H5CH2CH2NH3)2SnBr4\",\n        \"journal\": \"Zeitschrift f\\u00fcr Naturforschung\",\n        \"vol\": \"48 b\",\n        \"pages_start\": \"1013\",\n        \"pages_end\": \"1014\",\n        \"year\": \"1993\",\n        \"synthesis_starting_materials\": \"phenyl ethyl ammonium iodide (C6H5CH2CH2NH3I) and tin iodide (SnI2)\",\n        \"synthesis_product\": \"brown-golden plate-like (C6H5CH2CH2NH3)2SnI4 crystals\",\n        \"synthesis_description\": \"In an argon atmosphere, 540 mg (2.16 mmol) of C6H5CH2CH2NH3I was mixed with 373 mg (1 mmol) of SnI2 in 10 ml of acetonitrile under stirring. 4 ml of the solvent was evaporated by heating at 75 degrees C. The solution was then cooled to 10 degrees C. Finally, the precipitate was filtered and dried at 40 degrees celsius.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The spectrum was recorded on Varian model 2390 spectrophotometer\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1515/znb-1993-0727\",\n        \"dataset_ID\": 686,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Preparation and Characterization of (C6H5CH2CH2NH3)2SnI4 and (C6H5CH2CH2NH3)2SnBr4\",\n        \"journal\": \"Zeitschrift f\\u00fcr Naturforschung\",\n        \"vol\": \"48 b\",\n        \"pages_start\": \"1013\",\n        \"pages_end\": \"1014\",\n        \"year\": \"1993\",\n        \"synthesis_starting_materials\": \"phenyl ethyl ammonium iodide (C6H5CH2CH2NH3I) and tin iodide (SnI2)\",\n        \"synthesis_product\": \"brown-golden plate-like (C6H5CH2CH2NH3)2SnI4 crystals\",\n        \"synthesis_description\": \"In an argon atmosphere, 540 mg (2.16 mmol) of C6H5CH2CH2NH3I was mixed with 373 mg (1 mmol) of SnI2 in 10 ml of acetonitrile under stirring. 4 ml of the solvent was evaporated by heating at 75 degrees C. The solution was then cooled to 10 degrees C. Finally, the precipitate was filtered and dried at 40 degrees celsius.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using Jobin-Yvon model HG2S Raman spectrophoto\\u00admeter, using an argon laser.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7cc02408h\",\n        \"dataset_ID\": 687,\n        \"id\": 180,\n        \"compound_name\": \"Bis(phenethylammonium) cadmium iodide\",\n        \"formula\": \"C16H24N2CdI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CdI4, Cadmium iodide\",\n        \"iupac\": \"bis(phenylethanaminium) cadmium iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            692\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A near-room-temperature organic\\u2013inorganic hybrid ferroelectric: [C6H5CH2CH2NH3]2[CdI4]\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"5764\",\n        \"pages_end\": \"5766\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"methanol, CdI2 and 2-phenylethylammonium iodide\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"30 mL of methanol, 1.83 g of CdI2 and 2.49 g of 2-phenylethylammonium iodide (C6H5C2H4NH3I) was mixed together and stirred for 20 min. The 2-phenylethylammonium iodide was synthesized by mixing stoichiometric quantities of 2\\u2010phenylethylamine and hydroiodic acid (57%). The final crystals were obtained by the slow evaporation of the solution.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9dt00945k\",\n        \"dataset_ID\": 688,\n        \"id\": 181,\n        \"compound_name\": \"N,N-dimethylethanolammonium cadmium chloride\",\n        \"formula\": \"C4H12NOCdCl3\",\n        \"group\": \"N,N-dimethylethanolaminium trichlorocadmate(II), (DMEA)CdCl3, (C4H12NO)CdCl3\",\n        \"organic\": \"C4H12NO\",\n        \"inorganic\": \"CdCl3, Cadmium chloride\",\n        \"iupac\": \"N,N-dimethylethanolaminium cadmium chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ultra high phase transition temperature in a metal-halide perovskite-type material containing unprecedented hydrogen bonding interactions\",\n        \"journal\": \"Dalton Transactions\",\n        \"vol\": \"48\",\n        \"pages_start\": \"6621\",\n        \"pages_end\": \"6626\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N,N-dimethylethanolamine (DMEA), CdCl2 and HCl (37% concentrated)\",\n        \"synthesis_product\": \"colorless strip (DMEA)CdCl3 crystals\",\n        \"synthesis_description\": \"A solution mixture of DMEA (10 mmol), CdCl2 (10 mmol), and HCl (20 mmol) was slowly evaporated at room temperature for two weeks.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using Rigaku CCD diffractometer with Mo-K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9dt00945k\",\n        \"dataset_ID\": 689,\n        \"id\": 181,\n        \"compound_name\": \"N,N-dimethylethanolammonium cadmium chloride\",\n        \"formula\": \"C4H12NOCdCl3\",\n        \"group\": \"N,N-dimethylethanolaminium trichlorocadmate(II), (DMEA)CdCl3, (C4H12NO)CdCl3\",\n        \"organic\": \"C4H12NO\",\n        \"inorganic\": \"CdCl3, Cadmium chloride\",\n        \"iupac\": \"N,N-dimethylethanolaminium cadmium chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Infrared absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ultra high phase transition temperature in a metal-halide perovskite-type material containing unprecedented hydrogen bonding interactions\",\n        \"journal\": \"Dalton Transactions\",\n        \"vol\": \"48\",\n        \"pages_start\": \"6621\",\n        \"pages_end\": \"6626\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N,N-dimethylethanolamine (DMEA), CdCl2 and HCl (37% concentrated)\",\n        \"synthesis_product\": \"colorless strip (DMEA)CdCl3 crystals\",\n        \"synthesis_description\": \"A solution mixture of DMEA (10 mmol), CdCl2 (10 mmol), and HCl (20 mmol) was slowly evaporated at room temperature for two weeks.\",\n        \"experimental_method\": \"Infrared absorption\",\n        \"experimental_description\": \"The spectrum was recorded using a Shimadzu model IR-60 spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/science.aai8535\",\n        \"dataset_ID\": 690,\n        \"id\": 182,\n        \"compound_name\": \"Trimethylchloromethylammonium manganese chloride\",\n        \"formula\": \"(Me3NCH2Cl)MnCl3\",\n        \"group\": \"trimethylchloro-methanaminium trichloromanganate(II), TMCM-MnCl3\",\n        \"organic\": \"C4NH11Cl\",\n        \"inorganic\": \"MnCl3, manganese chloride\",\n        \"iupac\": \"trimethylchloro-methanaminium manganese chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"An organic-inorganic perovskite ferroelectric with large piezoelectric response\",\n        \"journal\": \"Science\",\n        \"vol\": \"357\",\n        \"pages_start\": \"306\",\n        \"pages_end\": \"309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Trimethylamine (30 wt % in water) and dichloromethane, acetonitrile, manganese(II) chloride (MnCl2)\",\n        \"synthesis_product\": \"red block-shaped Me3NCH2ClMnCl3 (TMCM-MnCl3) crystals\",\n        \"synthesis_description\": \"Equimolar amounts of Trimethylamine (30 wt% in water) and dichloromethane were mixed in acetonitrile and kept at room temperature for 24 hours. The obtained colorless solid ((Chloromethyl)trimethylammonium chloride) was collected.\\r\\nThe (Chloromethyl)trimethylammonium chloride (50 mmol) was then mixed with anhydrous MnCl2 (50 mmol) in 100 ml of methanol. Crystals were obtained by a slow evaporation. Film was then made by spin coating the solution on an ITO-glass substrate.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/science.aai8535\",\n        \"dataset_ID\": 691,\n        \"id\": 182,\n        \"compound_name\": \"Trimethylchloromethylammonium manganese chloride\",\n        \"formula\": \"(Me3NCH2Cl)MnCl3\",\n        \"group\": \"trimethylchloro-methanaminium trichloromanganate(II), TMCM-MnCl3\",\n        \"organic\": \"C4NH11Cl\",\n        \"inorganic\": \"MnCl3, manganese chloride\",\n        \"iupac\": \"trimethylchloro-methanaminium manganese chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"An organic-inorganic perovskite ferroelectric with large piezoelectric response\",\n        \"journal\": \"Science\",\n        \"vol\": \"357\",\n        \"pages_start\": \"306\",\n        \"pages_end\": \"309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Trimethylamine (30 wt % in water) and dichloromethane, acetonitrile, manganese(II) chloride (MnCl2)\",\n        \"synthesis_product\": \"red block-shaped Me3NCH2ClMnCl3 (TMCM-MnCl3) crystals\",\n        \"synthesis_description\": \"Equimolar amounts of Trimethylamine (30 wt% in water) and dichloromethane was mixed in acetonitrile at room temperature for 24 hours. The (Chloromethyl)trimethylammonium chloride (50 mmol) was then mixed with anhydrous manganese(II) (50 mmol) in 100 ml of methanol.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7cc02408h\",\n        \"dataset_ID\": 692,\n        \"id\": 180,\n        \"compound_name\": \"Bis(phenethylammonium) cadmium iodide\",\n        \"formula\": \"C16H24N2CdI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CdI4, Cadmium iodide\",\n        \"iupac\": \"bis(phenylethanaminium) cadmium iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            687\n        ],\n        \"primary_name\": \"Powder X-ray diffraction\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"2\\u03b8\",\n        \"secondary_unit\": \"(deg.)\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A near-room-temperature organic\\u2013inorganic hybrid ferroelectric: [C6H5CH2CH2NH3]2[CdI4]\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"5764\",\n        \"pages_end\": \"5766\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",\n        \"synthesis_product\": \"Colorless block-like crystals\",\n        \"synthesis_description\": \"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2\\u2010phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc00786a\",\n        \"dataset_ID\": 693,\n        \"id\": 183,\n        \"compound_name\": \"N-methyldabconium lead iodide\",\n        \"formula\": \"C7H15N2PbI3\",\n        \"group\": \"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",\n        \"organic\": \"C7H15N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N-methyldabconium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Extra thermo- and water-stable one-dimensional organic\\u2013inorganic hybrid perovskite [N-methyldabconium]PbI3 showing switchable dielectric behaviour, conductivity and bright yellow-green emission\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4321\",\n        \"pages_end\": \"4324\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"[N-methyldabconium]I, PbI2 and DMF\",\n        \"synthesis_product\": \"Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals\",\n        \"synthesis_description\": \"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using graphite-monochromated Mo Ka (\\u03bb = 0.71073 \\u00c5) radiation on a CCD area detector (Bruker SMART)\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc00786a\",\n        \"dataset_ID\": 694,\n        \"id\": 183,\n        \"compound_name\": \"N-methyldabconium lead iodide\",\n        \"formula\": \"C7H15N2PbI3\",\n        \"group\": \"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",\n        \"organic\": \"C7H15N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N-methyldabconium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Extra thermo- and water-stable one-dimensional organic\\u2013inorganic hybrid perovskite [N-methyldabconium]PbI3 showing switchable dielectric behaviour, conductivity and bright yellow-green emission\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4321\",\n        \"pages_end\": \"4324\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"[N-methyldabconium]I, PbI2 and DMF\",\n        \"synthesis_product\": \"[N-methyldabconium]PbI3\",\n        \"synthesis_description\": \"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc00786a\",\n        \"dataset_ID\": 695,\n        \"id\": 183,\n        \"compound_name\": \"N-methyldabconium lead iodide\",\n        \"formula\": \"C7H15N2PbI3\",\n        \"group\": \"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",\n        \"organic\": \"C7H15N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N-methyldabconium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Extra thermo- and water-stable one-dimensional organic\\u2013inorganic hybrid perovskite [N-methyldabconium]PbI3 showing switchable dielectric behaviour, conductivity and bright yellow-green emission\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4321\",\n        \"pages_end\": \"4324\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"[N-methyldabconium]I, PbI2 and DMF\",\n        \"synthesis_product\": \"Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals\",\n        \"synthesis_description\": \"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after slow evaporation at 333K after 2 weeks.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"The spectrum was recorded on a Shimadzu UV-3010 UV-vis-NIR spectrometer using BaSO4 as the reference of 100% reflectance.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b03095\",\n        \"dataset_ID\": 696,\n        \"id\": 184,\n        \"compound_name\": \"Dimethylammonium lead iodide\",\n        \"formula\": \"C2H8NPbI3\",\n        \"group\": \"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N-dimethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectric Properties, and Ionic Transport in the [(CH3)2NH2]PbI3 Organic\\u2013Inorganic Hybrid with 2H-Hexagonal Perovskite Structure\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"4918\",\n        \"pages_end\": \"4927\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(CH3)2NH, HI, PbI2 and DMAI\",\n        \"synthesis_product\": \"[(CH3)2NH2]PbI3\",\n        \"synthesis_description\": \"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 was then mixed and ground for 15 min.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b03095\",\n        \"dataset_ID\": 697,\n        \"id\": 184,\n        \"compound_name\": \"Dimethylammonium lead iodide\",\n        \"formula\": \"C2H8NPbI3\",\n        \"group\": \"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N-dimethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectric Properties, and Ionic Transport in the [(CH3)2NH2]PbI3 Organic\\u2013Inorganic Hybrid with 2H-Hexagonal Perovskite Structure\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"4918\",\n        \"pages_end\": \"4927\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(CH3)2NH, HI, PbI2 and DMAI\",\n        \"synthesis_product\": \"[(CH3)2NH2]PbI3\",\n        \"synthesis_description\": \"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 was then mixed and ground for 15 min.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b03095\",\n        \"dataset_ID\": 698,\n        \"id\": 184,\n        \"compound_name\": \"Dimethylammonium lead iodide\",\n        \"formula\": \"C2H8NPbI3\",\n        \"group\": \"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N-dimethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectric Properties, and Ionic Transport in the [(CH3)2NH2]PbI3 Organic\\u2013Inorganic Hybrid with 2H-Hexagonal Perovskite Structure\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"4918\",\n        \"pages_end\": \"4927\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(CH3)2NH solution (40 wt % in H2O), HI solution (57 wt % in H2O), PbI2 (99%)\",\n        \"synthesis_product\": \"yellow [(CH3)2NH2]PbI3 polycrystalline powder\",\n        \"synthesis_description\": \"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 were then mixed and ground for 15 min.\",\n        \"experimental_method\": \"UV\\u2212vis spectroscopy (Diffuse reflectance)\",\n        \"experimental_description\": \"The reflectance spectrum was recorded using a Jasco V-730 UV\\u2212visible double-beam spectrophotometer. The Kubelka\\u2212Munk equation F(R) = \\u03b1 = (1 \\u2212 R)^2/ 2R was used to convert reflectance to absorbance; here, R is the reflectance, and \\u03b1 is the absorption coefficients.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b00881\",\n        \"dataset_ID\": 699,\n        \"id\": 185,\n        \"compound_name\": \"Triethylpropylammonium lead iodide\",\n        \"formula\": \"C9H22PbI3\",\n        \"group\": \"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",\n        \"organic\": \"C9H22\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N,N-triethyl-N-propylaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectrics, Single-Ion Conductance, and Thermochromic Luminescence of a Inorganic\\u2212Organic Hybrid of [Triethylpropylammonium][PbI3]\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9525\",\n        \"pages_end\": \"9534\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Triethylpropylammonium iodide, PbI2, and DMF\",\n        \"synthesis_product\": \"yellow rod-like [triethylpropylammonium][PbI3] crystals\",\n        \"synthesis_description\": \"0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using Bruker SMART and the graphite- monochromated Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation on a CCD area detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b00881\",\n        \"dataset_ID\": 700,\n        \"id\": 185,\n        \"compound_name\": \"Triethylpropylammonium lead iodide\",\n        \"formula\": \"C9H22PbI3\",\n        \"group\": \"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",\n        \"organic\": \"C9H22\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N,N-triethyl-N-propylaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectrics, Single-Ion Conductance, and Thermochromic Luminescence of a Inorganic\\u2212Organic Hybrid of [Triethylpropylammonium][PbI3]\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9525\",\n        \"pages_end\": \"9534\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Triethylpropylammonium iodide, PbI2 and DMF\",\n        \"synthesis_product\": \"yellow rod-like [triethylpropylammonium][PbI3] crystals\",\n        \"synthesis_description\": \"0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using Bruker SMART and the graphite- monochromated Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation on a CCD area detector.\",\n        \"physical_property\": \"373.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b00881\",\n        \"dataset_ID\": 701,\n        \"id\": 185,\n        \"compound_name\": \"Triethylpropylammonium lead iodide\",\n        \"formula\": \"C9H22PbI3\",\n        \"group\": \"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",\n        \"organic\": \"C9H22\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N,N-triethyl-N-propylaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectrics, Single-Ion Conductance, and Thermochromic Luminescence of a Inorganic\\u2212Organic Hybrid of [Triethylpropylammonium][PbI3]\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9525\",\n        \"pages_end\": \"9534\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Triethylpropylammonium iodide, PbI2 and DMF\",\n        \"synthesis_product\": \"yellow rod-like [triethylpropylammonium][PbI3] crystals\",\n        \"synthesis_description\": \"0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using Bruker SMART and the graphite- monochromated Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation on a CCD area detector.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b00881\",\n        \"dataset_ID\": 702,\n        \"id\": 185,\n        \"compound_name\": \"Triethylpropylammonium lead iodide\",\n        \"formula\": \"C9H22PbI3\",\n        \"group\": \"N,N,N-triethyl-N-propylaminium triiodoplumbate(II), [triethylpropylammonium][PbI3]\",\n        \"organic\": \"C9H22\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N,N-triethyl-N-propylaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectrics, Single-Ion Conductance, and Thermochromic Luminescence of a Inorganic\\u2212Organic Hybrid of [Triethylpropylammonium][PbI3]\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9525\",\n        \"pages_end\": \"9534\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Triethylpropylammonium iodide, PbI2, and DMF\",\n        \"synthesis_product\": \"yellow rod-like [triethylpropylammonium][PbI3] crystals\",\n        \"synthesis_description\": \"0.003 mol of PbI2 and 0.003 mol of Triethylpropylammonium iodide were mixed in 15 mL of DMF under ultrasonic conditions. Single crystals were obtained after two weeks from a slow evaporation.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The spectrum was recorded using a PerkinElmer Lambda 950 UV\\u2212vis\\u2212near-IR spectrophotometer\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b03217\",\n        \"dataset_ID\": 703,\n        \"id\": 186,\n        \"compound_name\": \"Heptakis(dimethylammonium) lead bromide\",\n        \"formula\": \"C14H54N7Pb4Br15\",\n        \"group\": \"heptakis(dimethanaminium) pentadecabromo tetraplumbate(II), DMA7Pb4Br15, [(CH3)2NH2]7Pb4Br15\",\n        \"organic\": \"C2H9N\",\n        \"inorganic\": \"Pb4Br15, Lead bromide\",\n        \"iupac\": \"heptakis(dimethanaminium) lead bromide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)2NH2]7Pb4X15 (X = Cl\\u2212 and Br\\u2212), 2D-Perovskite Related Hybrids with Dielectric Transitions and Broadband Photoluminiscent Emission\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"57\",\n        \"pages_start\": \"3215\",\n        \"pages_end\": \"3222\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2 (99%), (CH3)2NH solution (40 wt % in H2O), DMF, HBr solution (48 wt % in H2O)\",\n        \"synthesis_product\": \"Colorless plate-like DMA7Pb4Br15 crystals\",\n        \"synthesis_description\": \"(CH3)2NH2Br (DMABr) was synthesized by reacting (CH3)2NH with HBr in an ice bath, followed by rotary evaporation, and washed with diethyl ether. 4 mmol of PbBr2 and 7 mmol of DMABr were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Bruker Kappa X-ray diffractometer equipped with an Apex II CCD detector and using monochromatic Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"275.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b03217\",\n        \"dataset_ID\": 704,\n        \"id\": 186,\n        \"compound_name\": \"Heptakis(dimethylammonium) lead bromide\",\n        \"formula\": \"C14H54N7Pb4Br15\",\n        \"group\": \"heptakis(dimethanaminium) pentadecabromo tetraplumbate(II), DMA7Pb4Br15, [(CH3)2NH2]7Pb4Br15\",\n        \"organic\": \"C2H9N\",\n        \"inorganic\": \"Pb4Br15, Lead bromide\",\n        \"iupac\": \"heptakis(dimethanaminium) lead bromide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)2NH2]7Pb4X15 (X = Cl\\u2212 and Br\\u2212), 2D-Perovskite Related Hybrids with Dielectric Transitions and Broadband Photoluminiscent Emission\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"57\",\n        \"pages_start\": \"3215\",\n        \"pages_end\": \"3222\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2 (99%), (CH3)2NH solution (40 wt % in H2O), DMF, HBr solution (48 wt % in H2O)\",\n        \"synthesis_product\": \"Colorless plate-like DMA7Pb4Br15 crystals\",\n        \"synthesis_description\": \"(CH3)2NH2Br (DMABr) was synthesized by reacting (CH3)2NH with HBr in an ice bath, followed by rotary evaporation, and washed with diethyl ether.\\r\\n4 mmol of PbBr2 and 7 mmol of DMABr were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature. \\r\\nThe crystals were ground to prepare the powder.\",\n        \"experimental_method\": \"UV-vis absorbance (diffuse reflectance)\",\n        \"experimental_description\": \"Reflectance was recorded using a Jasco V-730 UV\\u2212visible double-beam spectrophotometer. The reflectance data were converted to absorbance using the Kubelka\\u2212Munk equation: F(R)= \\u03b1 = (1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 is the absorption coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b03217\",\n        \"dataset_ID\": 705,\n        \"id\": 187,\n        \"compound_name\": \"Heptakis(dimethylammonium) lead chloride\",\n        \"formula\": \"C14H54N7Pb4Cl15\",\n        \"group\": \"heptakis(bimethanaminium) pentadecachloro tetraplumbate(II), DMA7Pb4Cl15, [(CH3)2NH2]7Pb4Cl15\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"Pb4Cl15, Lead chloride\",\n        \"iupac\": \"heptakis(bimethanaminium) lead chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)2NH2]7Pb4X15 (X = Cl\\u2212 and Br\\u2212), 2D-Perovskite Related Hybrids with Dielectric Transitions and Broadband Photoluminiscent Emission\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"57\",\n        \"pages_start\": \"3215\",\n        \"pages_end\": \"3222\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbCl2 (99%), (CH3)2NH2Cl (99%) (DMACl), DMF, HCl solution (37 wt % in H2O)\",\n        \"synthesis_product\": \"Colorless DMA7Pb4Cl15 crystals\",\n        \"synthesis_description\": \"4 mmol of PbCl2 and 7 mmol of DMACl were mixed in 5 mL of DMF. Single crystals of the final product were obtained after a slow evaporation for a few days at room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Bruker Kappa X-ray diffractometer equipped with an Apex II CCD detector and using monochromatic Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"275.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b03217\",\n        \"dataset_ID\": 706,\n        \"id\": 187,\n        \"compound_name\": \"Heptakis(dimethylammonium) lead chloride\",\n        \"formula\": \"C14H54N7Pb4Cl15\",\n        \"group\": \"heptakis(bimethanaminium) pentadecachloro tetraplumbate(II), DMA7Pb4Cl15, [(CH3)2NH2]7Pb4Cl15\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"Pb4Cl15, Lead chloride\",\n        \"iupac\": \"heptakis(bimethanaminium) lead chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)2NH2]7Pb4X15 (X = Cl\\u2212 and Br\\u2212), 2D-Perovskite Related Hybrids with Dielectric Transitions and Broadband Photoluminiscent Emission\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"57\",\n        \"pages_start\": \"3215\",\n        \"pages_end\": \"3222\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbCl2 (99%), (CH3)2NH2Cl (99%) (DMACl), DMF, HCl solution (37 wt % in H2O)\",\n        \"synthesis_product\": \"Colorless DMA7Pb4Cl15 crystals\",\n        \"synthesis_description\": \"4 mmol of PbCl2 and 7 mmol of DMACl were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature. The crystals were ground to prepare the powder.\",\n        \"experimental_method\": \"UV-vis absorbance (diffuse reflectance)\",\n        \"experimental_description\": \"Reflectance was recorded using a Jasco V-730 UV\\u2212visible double-beam spectrophotometer. The reflectance data were converted to absorbance using the Kubelka\\u2212Munk equation: F(R)= \\u03b1 = (1 \\u2212 R)^2/2R, where R is the reflectance and \\u03b1 is the absorption coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b03217\",\n        \"dataset_ID\": 708,\n        \"id\": 187,\n        \"compound_name\": \"Heptakis(dimethylammonium) lead chloride\",\n        \"formula\": \"C14H54N7Pb4Cl15\",\n        \"group\": \"heptakis(bimethanaminium) pentadecachloro tetraplumbate(II), DMA7Pb4Cl15, [(CH3)2NH2]7Pb4Cl15\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"Pb4Cl15, Lead chloride\",\n        \"iupac\": \"heptakis(bimethanaminium) lead chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)2NH2]7Pb4X15 (X = Cl\\u2212 and Br\\u2212), 2D-Perovskite Related Hybrids with Dielectric Transitions and Broadband Photoluminiscent Emission\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"57\",\n        \"pages_start\": \"3215\",\n        \"pages_end\": \"3222\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbCl2 (99%), (CH3)2NH2Cl (99%) (DMACl), DMF, HCl solution (37 wt % in H2O)\",\n        \"synthesis_product\": \"Colorless DMA7Pb4Cl15 crystals\",\n        \"synthesis_description\": \"4 mmol of PbCl2 and 7 mmol of DMACl were mixed in 5 mL of DMF. Single crystals of the final product were obtained after a slow evaporation for a few days at room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using a Horiba FluoroMax Plus-P spectrofluorometer equipped with an R928P photon-counting emission detector. The excitation source was a 150 W ozone-free Xe arc lamp. A lamp reference correction was applied.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b03217\",\n        \"dataset_ID\": 710,\n        \"id\": 186,\n        \"compound_name\": \"Heptakis(dimethylammonium) lead bromide\",\n        \"formula\": \"C14H54N7Pb4Br15\",\n        \"group\": \"heptakis(dimethanaminium) pentadecabromo tetraplumbate(II), DMA7Pb4Br15, [(CH3)2NH2]7Pb4Br15\",\n        \"organic\": \"C2H9N\",\n        \"inorganic\": \"Pb4Br15, Lead bromide\",\n        \"iupac\": \"heptakis(dimethanaminium) lead bromide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)2NH2]7Pb4X15 (X = Cl\\u2212 and Br\\u2212), 2D-Perovskite Related Hybrids with Dielectric Transitions and Broadband Photoluminiscent Emission\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"57\",\n        \"pages_start\": \"3215\",\n        \"pages_end\": \"3222\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2 (99%), (CH3)2NH solution (40 wt % in H2O), DMF, HBr solution (48 wt % in H2O)\",\n        \"synthesis_product\": \"Colorless plate-like DMA7Pb4Br15 crystals\",\n        \"synthesis_description\": \"(CH3)2NH2Br (DMABr) was synthesized by reacting (CH3)2NH with HBr in an ice bath, followed by rotary evaporation, and washed with diethyl ether. 4 mmol of PbBr2 and 7 mmol of DMABr were mixed in 5 mL of DMF. Single crystals of the final product were obtained after slow evaporation for a few days at room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using a Horiba FluoroMax Plus-P spectrofluorometer equipped with an R928P photon-counting emission detector. The excitation source was a 150 W ozone-free Xe arc lamp. A lamp reference correction was applied.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adfm.201903528\",\n        \"dataset_ID\": 711,\n        \"id\": 188,\n        \"compound_name\": \"Methylammonium germanium bromide\",\n        \"formula\": \"CH6NGeBr3\",\n        \"group\": \"Methanaminium tribromogermanate(II), MAGeBr3, CH3NH3GeBr3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"GeBr3, Germanium bromide\",\n        \"iupac\": \"methanaminium germanium bromide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered Germanium Hybrid Perovskite Bromides: Insights from Experiments and First\\u2010Principles Calculations\",\n        \"journal\": \"Advanced Functional Materials\",\n        \"vol\": \"29\",\n        \"pages_start\": \"1903528-1\",\n        \"pages_end\": \"1903528-9\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"HBr, H3PO2, GeO2, CH3NH3Br\",\n        \"synthesis_product\": \"CH3NH3GeBr3\",\n        \"synthesis_description\": \"All operations were carried out under high purity nitrogen. A two-neck flask was charged with a mixture of 48% w/w aqueous HBr (3.0 mL, 55.2 mmol) and 50% w/w aqueous H3PO2(2.0 mL, 18.2 mmol). GeO2 powder (209 mg, 2 mmol) was dissolved in the mixture by heating the flask to 140 \\u00b0C in an oil bath, under constant magnetic stirring for about 20 min, which formed a bright pale-yellow solution. Subsequently, a stoichiometric amount of solid CH3NH3Br (224 mg, 2 mmol) was added to the hot solution and dissolved then. 20 min later, the stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, lemon yellow, granular crystals were precipitated. After being kept in the solution overnight, the crystals were collected by suction filtration and dried under reduced pressure\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adfm.201903528\",\n        \"dataset_ID\": 712,\n        \"id\": 189,\n        \"compound_name\": \"Butylammonium germanium bromide\",\n        \"formula\": \"C4H12NGeBr4\",\n        \"group\": \"Butan-1-aminium tetrabromogermanate(II), BA2GeBr4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"GeBr4, Germanium bromide\",\n        \"iupac\": \"butan-1-aminium germanium bromide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered Germanium Hybrid Perovskite Bromides: Insights from Experiments and First\\u2010Principles Calculations\",\n        \"journal\": \"Advanced Functional Materials\",\n        \"vol\": \"29\",\n        \"pages_start\": \"1903528-1\",\n        \"pages_end\": \"1903528-9\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"HBr, H3PO2, GeO2, n\\u2212  CH3(CH2)3NH2, n\\u2212  CH3(CH2)3NH3Br\",\n        \"synthesis_product\": \"C4H12NGeBr4\",\n        \"synthesis_description\": \"A two-neck flask was charged with a mixture of 48% w/w aqueous HBr (2.0 mL, 36.8 mmol) and 50% w/w aqueous H3PO2 (3.0 mL, 27.3 mmol). GeO2 powder (209 mg, 2 mmol) was dissolved in the mixture by heating the flask to 140 \\u00b0C in an oil bath, under constant magnetic stirring for about 20 min, which formed a bright pale-yellow solution. In a separate flask, n\\u2212 CH3(CH2)3NH2(197 \\u03bcL, 2 mmol) was neutralized with 48% w/w aqueous HBr (2 mL, 36.8 mmol) in an ice bath, resulting a transparent solution. The n\\u2212 CH3(CH2)3NH3Br solution was then added dropwise into the two-neck flask. After being gradually heated to about 160 \\u00b0C in 30 min, the stirring was discontinued, and the solution was left to cool down to freezing temperature, resulting in the precipitation of white lamellar crystals. After being kept in the solution overnight, the crystals were collected by suction filtration and dried under reduced pressure.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.materresbull.2017.09.054\",\n        \"dataset_ID\": 713,\n        \"id\": 190,\n        \"compound_name\": \"Methylammonium tin chloride\",\n        \"formula\": \"CH6NSnCl3\",\n        \"group\": \"Methanaminium trichlorostannate(II), MASnCl3, CH3NH3SnCl3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"SnCl3, Tin chloride\",\n        \"iupac\": \"methanaminium tin chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New class of lead free perovskite material for low-cost solar cell application\",\n        \"journal\": \"Materials Research Bulletin\",\n        \"vol\": \"97\",\n        \"pages_start\": \"572\",\n        \"pages_end\": \"577\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"HCl, methylamine, SnCl2\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Initially, methyl ammonium chloride (CH3NH3Cl) was synthesized by mixing 32.3 ml of HCl acid in 30 ml of methylamine. Powder of CH3NH3Cl was dissolved in the ethanol and was heated at 60 \\u00b0C for four hours. The solution was frozen in the refrigerator for 3-5 days.  The obtained crystals were filtered.\\r\\n\\r\\nCH3NH3Cl powder (0.395 gm) and SnCl2 (1.157 gm) were mixed in 2 ml DMF and kept for stirring at 60 \\u00b0C for 8 h.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A UV-vis spectrophotometer (Model no. UV-1800,SHIMADZU) was used to measure the UV-vis absorption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C5RA21291J\",\n        \"dataset_ID\": 714,\n        \"id\": 191,\n        \"compound_name\": \"Methylammonium tin bromide\",\n        \"formula\": \"CH6NSnBr3\",\n        \"group\": \"Methanaminium tribromostannate(II), MASnBr3, (CH3NH3)SnBr3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"SnBr3, Tin bromide\",\n        \"iupac\": \"methanaminium tin bromide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Properties and solar cell applications of Pb-free perovskite films formed by vapor deposition\",\n        \"journal\": \"RSC Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"2819\",\n        \"pages_end\": \"2825\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnBr2 (tin(ii) bromide, 99.4%, Alfa Aesar), MABr (methylammonium bromide, CH3NH3Br, DYESOL), TiO2/FTO substrate\",\n        \"synthesis_product\": \"400 nm thick MASnBr3 film\",\n        \"synthesis_description\": \"The film was fabricated by vapor deposition of SnBr2 and MABr at a ratio of 4\\u2006:\\u20061 (0.4 \\u00c5 s\\u22121\\u2006:\\u20060.1 \\u00c5 s\\u22121).\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The spectrum was measured using an Evolution 600 UV-Vis spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.nanoen.2016.09.009\",\n        \"dataset_ID\": 715,\n        \"id\": 192,\n        \"compound_name\": \"Cesium tin bromide\",\n        \"formula\": \"CsSnBr3\",\n        \"group\": \"Cesium tribromostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnBr3\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-23\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"All vapor-deposited lead-free doped CsSnBr3 planar solar cells\",\n        \"journal\": \"Nano Energy\",\n        \"vol\": \"28\",\n        \"pages_start\": \"469\",\n        \"pages_end\": \"474\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnBr2 (Alfa Aesar 99.4%), SnF2 and CsBr\",\n        \"synthesis_product\": \"yellow 97 nm thick CsSnBr3 film on glass\",\n        \"synthesis_description\": \"For the perovskite layer, the desired thicknesses of SnBr2, SnF2, and CsBr were vapor-deposited at a rate of ~0.5\\u01fa/s under a base pressure of ~10\\u22126 Torr.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1007/s12274-016-1051-8\",\n        \"dataset_ID\": 716,\n        \"id\": 193,\n        \"compound_name\": \"Formamidinium tin bromide iodide\",\n        \"formula\": \"CH5N2SnI2Br\",\n        \"group\": \"FASnI2Br, HC(NH2)2SnI2Br, diaminomethanide monobromo diiodostannate(II)\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"SnI2Br, Tin bromide iodide\",\n        \"iupac\": \"diaminomethanide tin bromide iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Low-temperature processed solar cells with formamidinium tin halide perovskite/fullerene heterojunctions\",\n        \"journal\": \"Nano Research\",\n        \"vol\": \"9\",\n        \"pages_start\": \"1570\",\n        \"pages_end\": \"1577\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnI2 (Sigma-Aldrich), FABr (Dyesol), N,N-dimethylformamide (anhydrous, Sigma-Aldrich), ITO/PEDOT:PSS substrate, chlorobenzene\",\n        \"synthesis_product\": \"200 nm FASnI2Br film\",\n        \"synthesis_description\": \"373 mg of SnI2 and 125 mg of FABr in 1 ml N,N-dimethylformamide were mixed. This precursor solution was spin-coated at 2,500 rpm. 20 \\u03bcL of chlorobenzene was dropped onto the spinning substrate 7 s after starting the spin-coating. The film was annealed at 75 \\u00b0C for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The absorption spectrum was recorded using V-650, Jasco spectrophotometer with an integrating sphere.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1016/j.mseb.2004.12.052\",\n        \"dataset_ID\": 717,\n        \"id\": 194,\n        \"compound_name\": \"Bis(butylammonium) copper chloride\",\n        \"formula\": \"C8H24N2CuCl4\",\n        \"group\": \"(C4H9NH3)2CuCl4, bis(butan-1-aminium) tetrachlorocuprate(II)\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"bis(butan-1-aminium) copper chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Preparation and characterization of organic\\u2013inorganic hybrid perovskite (C4H9NH3)2CuCl4\",\n        \"journal\": \"Materials Science and Engineering: B\",\n        \"vol\": \"117\",\n        \"pages_start\": \"313\",\n        \"pages_end\": \"316\",\n        \"year\": \"2005\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"The organic\\u2013inorganic hybrid perovskite, (C4H9NH3)2CuCl4, was prepared by the reaction of butylammonium chloride, C4H9NH3Cl, with a stoichiometric amount of copper chloride. Firstly, anhydrous CuCl2 powder was added to the solution of C4H9NH3Cl in anhydrous ethanol, and the reaction mixture was stirred and refluxed for 1 h. The solvent was then evaporated completely, giving golden solids. The solids were recrystallized in anhydrous ethanol and dried at 80 \\u00b0C in vacuum, obtaining (C4H9NH3)2CuCl4 as golden sheet-like crystals. Calcd for C8H24N2CuCl4: C, 27.16%; N, 7.92%; H, 6.79%. Found: C, 27.21%; N, 7.84%; H, 6.66%.\\r\\n\\r\\nThe (C4H9NH3)2CuCl4 film was prepared by spin-coating a solution (10 mg/ml) of (C4H9NH3)2CuCl4 in anhydrous ethanol on a quartz substrate at a speed of 800 rpm for 30 s, followed by annealing at 80 \\u00b0C in vacuum for 1 h. The film thickness was tested about 100 nm.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01564\",\n        \"dataset_ID\": 718,\n        \"id\": 195,\n        \"compound_name\": \"Bis(4-fluorophenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H18F2N2PbI4\",\n        \"group\": \"(F-PMA)2PbI4, 4-fluorophenylmethylammonium lead iodide, (C14H18F2N2)PbI4, 4-fluorophenylmethanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C7H9FN\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-fluorophenylmethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures of (4-Y\\u2011C6H4CH2NH3)2PbI4 {Y = H, F, Cl, Br, I}: Tuning of Hybrid Organic Inorganic Perovskite Structures from Ruddlesden\\u2212 Popper to Dion\\u2212Jacobson Limits\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"6145\",\n        \"pages_end\": \"6153\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, 57 wt % HI aqueous solution, F-PMA, MeOH\",\n        \"synthesis_product\": \"Dark orange crystal\",\n        \"synthesis_description\": \"131 mg PbI2 was dissolved in 1ml HI, under stirring at 100 \\u00b0C for 2 min. Then, 65 mg F-PMA in 1 mL HI and 0.8 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 \\u00b0C for 2 min before the solution was cooled to room temperature and was left for 12h. \\r\\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (F-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction.\",\n        \"experimental_description\": \"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 100 K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\",\n        \"physical_property\": \"106.0 (\\u00b16.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01564\",\n        \"dataset_ID\": 719,\n        \"id\": 196,\n        \"compound_name\": \"Bis(4-chlorophenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H18Cl2N2PbI4\",\n        \"group\": \"(Cl-PMA)2PbI4, 4-chlorophenylmethanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C7H9ClN\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-chlorophenylmethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures of (4-Y\\u2011C6H4CH2NH3)2PbI4 {Y = H, F, Cl, Br, I}: Tuning of Hybrid Organic Inorganic Perovskite Structures from Ruddlesden\\u2212 Popper to Dion\\u2212Jacobson Limits\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"6145\",\n        \"pages_end\": \"6153\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, 57 wt % HI aqueous solution, Cl-PMA, MeOH\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"124 mg PbI2 was dissolved in 2 ml HI, under stirring at 100 \\u00b0C for 2 min. Then, 78 mg Cl-PMA in 2 mL HI and 1.2 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 \\u00b0C for 2 min before the solution was cooled to room temperature and was left for 12h. \\r\\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (Cl-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction.\",\n        \"experimental_description\": \"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 220K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\",\n        \"physical_property\": \"225.0 (\\u00b10.1)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01564\",\n        \"dataset_ID\": 720,\n        \"id\": 197,\n        \"compound_name\": \"Bis(4-bromophenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H18Br2N2PbI4\",\n        \"group\": \"(Br-PMA)2PbI4, 4-bromophenylmethanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C7H9BrN\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-bromophenylmethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures of (4-Y\\u2011C6H4CH2NH3)2PbI4 {Y = H, F, Cl, Br, I}: Tuning of Hybrid Organic Inorganic Perovskite Structures from Ruddlesden\\u2212 Popper to Dion\\u2212Jacobson Limits\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"6145\",\n        \"pages_end\": \"6153\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, 57 wt % HI aqueous solution, Br-PMA, MeOH\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"127 mg PbI2 was dissolved in 2 ml HI, under stirring at 100 \\u00b0C for 2 min. Then, 103 mg Br-PMA in 2 mL HI and 1.2 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 \\u00b0C for 2 min before the solution was cooled to room temperature and was left for 12h. \\r\\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (Br-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction.\",\n        \"experimental_description\": \"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 100 K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\",\n        \"physical_property\": \"104.0 (\\u00b10.8)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01564\",\n        \"dataset_ID\": 721,\n        \"id\": 198,\n        \"compound_name\": \"Bis(4-iodophenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H18I2N2PbI4\",\n        \"group\": \"(I-PMA)2PbI4, 4-iodophenylmethanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C7H9IN\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-iodophenylmethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structures of (4-Y\\u2011C6H4CH2NH3)2PbI4 {Y = H, F, Cl, Br, I}: Tuning of Hybrid Organic Inorganic Perovskite Structures from Ruddlesden\\u2212 Popper to Dion\\u2212Jacobson Limits\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"6145\",\n        \"pages_end\": \"6153\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, 57 wt % HI aqueous solution, I-PMA, MeOH\",\n        \"synthesis_product\": \"Orange plate-like crystal\",\n        \"synthesis_description\": \"202 mg PbI2 was dissolved in 4 ml HI, under stirring at 100 \\u00b0C for 2 min. Then, 197 mg I-PMA in 0.3 mL HI and 4 mL MeOH was added to the hot PbI2 solution. The mixture was stirred at 130 \\u00b0C for 2 min before the solution was cooled to room temperature and was left for 12h. \\r\\nTo obtain single crystals, 25 mg PbI2 was added to 1mL HI, into which 2 mL MeOH was added on top. (Br-PMA)2PbI4 crystals were dissolved in a minimum of MeOH and slowly added. The crystals appear at the interface between the HI and MeOH after about 24h.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction.\",\n        \"experimental_description\": \"XtaLAB Synergy-S, Dualflex, HyPix diffractometer was used to collect X-ray diffraction. The crystals were heated to about 100 K during data collection. OLEX2 and ShelXT41 were used to resolve the crystal structure. ShelXL42 was used to refine the structure by least-squares minimization.\",\n        \"physical_property\": \"100.0 (\\u00b10.1)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b07712\",\n        \"dataset_ID\": 722,\n        \"id\": 199,\n        \"compound_name\": \"1,8-octyldiammonium methylammonium lead iodide\",\n        \"formula\": \"C9H28N3Pb2I7\",\n        \"group\": \"(NH3C8H16NH3)(MA)Pb2I7, 1,8-octanediaminium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C8H22N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"1,8-octanediaminium methanaminium lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Halide Perovskites Incorporating Straight Chain Symmetric Diammonium Ions, (NH3CmH2mNH3)(CH3NH3)n\\u22121PbnI3n+1 (m =4\\u22129; n =1\\u22124)\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"140\",\n        \"pages_start\": \"12226\",\n        \"pages_end\": \"12238\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,8-diaminooctane (98%) from Sigma-Aldrich\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"223.2 mg PbO and 33.75 mg CH3NH2\\u00b7HCl were added into a mixture of 1.5 mL of HI solution and 0.3 mL of H3PO2 solution under boiling temperature and vigorous stirring. \\r\\nAfter obtaining a clear yellow solution, 120 mg NH3C8H16NH3I2  was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 \\u00b0C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75\\u00b0C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b07712\",\n        \"dataset_ID\": 723,\n        \"id\": 200,\n        \"compound_name\": \"1,8-octyldiammonium bis(methylammonium) lead iodide\",\n        \"formula\": \"C10H34N4Pb3I10\",\n        \"group\": \"(NH3C8H16NH3)(MA)2Pb3I10, 1,8-octanediaminium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C8H22N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"1,8-octanediaminium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Halide Perovskites Incorporating Straight Chain Symmetric Diammonium Ions, (NH3CmH2mNH3)(CH3NH3)n\\u22121PbnI3n+1 (m =4\\u22129; n =1\\u22124)\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"140\",\n        \"pages_start\": \"12226\",\n        \"pages_end\": \"12238\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,8-diaminooctane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",\n        \"synthesis_product\": \"dark red plate-shaped crystals\",\n        \"synthesis_description\": \"334.8 mg PbO and 67.5 mg CH3NH2\\u00b7HCl were added into a mixture of 2.5 mL of HI solution and 0.5 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 112 mg NH3C8H16NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 \\u00b0C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75\\u00b0C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b07712\",\n        \"dataset_ID\": 724,\n        \"id\": 201,\n        \"compound_name\": \"1,8-octyldiammonium tris(methylammonium) lead iodide\",\n        \"formula\": \"C11H40N5Pb4I13\",\n        \"group\": \"(NH3C8H16NH3)(MA)3Pb4I13, 1,8-octanediaminium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C8H22N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"1,8-octanediaminium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Halide Perovskites Incorporating Straight Chain Symmetric Diammonium Ions, (NH3CmH2mNH3)(CH3NH3)n\\u22121PbnI3n+1 (m =4\\u22129; n =1\\u22124)\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"140\",\n        \"pages_start\": \"12226\",\n        \"pages_end\": \"12238\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,8-diaminooctane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",\n        \"synthesis_product\": \"black plate-shaped crystals\",\n        \"synthesis_description\": \"446.4 mg PbO and 101.28 mg CH3NH2\\u00b7HCl were added into a mixture of 4 mL of HI solution and 0.8 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 80 mg  NH3C8H16NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 \\u00b0C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75\\u00b0C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b07712\",\n        \"dataset_ID\": 725,\n        \"id\": 202,\n        \"compound_name\": \"1,9-nonyldiammonium lead iodide\",\n        \"formula\": \"C9H24N6PbI4\",\n        \"group\": \"(NH3C9H18NH3)PbI4, NH3C9H18NH3PbI4, 1,9-nonanediaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C9H24N6\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1,9-nonanediaminium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Halide Perovskites Incorporating Straight Chain Symmetric Diammonium Ions, (NH3CmH2mNH3)(CH3NH3)n\\u22121PbnI3n+1 (m =4\\u22129; n =1\\u22124)\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"140\",\n        \"pages_start\": \"12226\",\n        \"pages_end\": \"12238\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,9-diaminononane (98%), from Sigma-Aldrich.\",\n        \"synthesis_product\": \"orange plate-shaped crystals\",\n        \"synthesis_description\": \"44.6 mg PbO was added into a mixture of 2 mL of HI solution and 0.4 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 82.8 mg  NH3C9H18NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 \\u00b0C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75\\u00b0C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5) operating at 50 kV and 40 mA were used to collect single-crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b07712\",\n        \"dataset_ID\": 726,\n        \"id\": 203,\n        \"compound_name\": \"1,9-nonyldiammonium methylammonium lead iodide\",\n        \"formula\": \"C10H30N7Pb2I7\",\n        \"group\": \"(NH3C9H18NH3)(MA)Pb2I7, 1,9-nonanediaminium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C9H24N6, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"1,9-nonanediaminium methanaminium lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Halide Perovskites Incorporating Straight Chain Symmetric Diammonium Ions, (NH3CmH2mNH3)(CH3NH3)n\\u22121PbnI3n+1 (m =4\\u22129; n =1\\u22124)\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"140\",\n        \"pages_start\": \"12226\",\n        \"pages_end\": \"12238\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,9-diaminononane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"223.2 mg PbO and 33.75 mg CH3NH2\\u00b7HCl were added into a mixture of 2 mL of HI solution and 0.4 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 74.5 mg  NH3C9H18NH3I2  was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 \\u00b0C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75\\u00b0C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5) operating at 50 kV and 40 mA were used to collect single crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption. Jana 2006 package was used to reslove structure. PLATON44 was used to validate space groups and twinning domains of the compounds.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b07712\",\n        \"dataset_ID\": 727,\n        \"id\": 204,\n        \"compound_name\": \"1,9-nonyldiammonium bis(methylammonium) lead iodide\",\n        \"formula\": \"C11H36N8Pb3I10\",\n        \"group\": \"(NH3C9H18NH3)(MA)2Pb3I10, 1,9-nonanediaminium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C9H24N6, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"1,9-nonanediaminium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Halide Perovskites Incorporating Straight Chain Symmetric Diammonium Ions, (NH3CmH2mNH3)(CH3NH3)n\\u22121PbnI3n+1 (m =4\\u22129; n =1\\u22124)\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"140\",\n        \"pages_start\": \"12226\",\n        \"pages_end\": \"12238\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O), hypophosphorous acid solution (50 wt % in H2O), 1,9-diaminononane (98%) from Sigma-Aldrich. Methylammonium iodide (MAI) was synthesized from 57 wt%  aqueous hydriodic acid (HI) and 40 wt% aqueous methylamine (CH3NH2).\",\n        \"synthesis_product\": \"dark red plate-shaped crystals\",\n        \"synthesis_description\": \"334.8 mg PbO and 67.5 mg CH3NH2\\u00b7HCl were added into a mixture of 3.5 mL of HI solution and 0.7 mL of H3PO2 solution under boiling temperature and vigorous stirring. After obtaining a clear yellow solution, 58 mg  NH3C9H18NH3I2 was then dissolved into the above hot solution. Light-yellow powder precipitation formed in the solution and then re-dissolved into the solution under heating and stirring for 15 min. The temperature was then dropped to 125 \\u00b0C, which is right below the boiling point of HI. After the complete precipitation of the crystal at 75\\u00b0C, the hot plate was turned off and the solution was left to cool to room temperature. The final product was filtered by suction filtration and dried on the filtration funnel for 30 min.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5) operating at 50 kV and 40 mA were used to collect single crystal diffraction data. X-AREA, X-RED, and XSHAPE programs were used to integrate and correct numerical absorption. Jana 2006 package was used to reslove structure. PLATON44 was used to validate space groups and twinning domains of the compounds.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.jpclett.7b00086\",\n        \"dataset_ID\": 728,\n        \"id\": 205,\n        \"compound_name\": \"Aniline copper bromide iodide\",\n        \"formula\": \"C6H6NCuBr2I\",\n        \"group\": \"C6H4NH2CuBr2I, aniline monobromo diiodocuprate(II)\",\n        \"organic\": \"C6H6N\",\n        \"inorganic\": \"CuBr2I, Copper bromide iodide\",\n        \"iupac\": \"aniline copper bromide iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic\\u2013Inorganic Copper(II)-Based Material: A Low-Toxic, Highly Stable Light Absorber for Photovoltaic Application\",\n        \"journal\": \"J. Phys. Chem. Lett.\",\n        \"vol\": \"8\",\n        \"pages_start\": \"1804\",\n        \"pages_end\": \"1809\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"CuBr2 (Copper bromide,99.999% Sigma-Aldrich), C6H4NH2I (2-iodoaniline, 98% Aladdin), N, N-Dimethylformamide, FTO substrate\",\n        \"synthesis_product\": \"500 nm thick C6H4NH2CuBr2I thin-film on FTO glass\",\n        \"synthesis_description\": \"An equimolar mixture of C6H4NH2I (547.55 mg) and CuBr2 (558.75 mg) was dissolved in N, N-Dimethylformamide (1 mL) by stirring at 60 \\u00b0C overnight. The solution was ultrasonicated for 30 min and filtered by PTFE syringe filters (0.45 \\u03bcm).\\r\\nThe obtained solution was spin-coated at 1500 rpm for 30 s, followed by annealing on a hot plate at 70 \\u00b0C for 30 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The spectrum was measured using PerkinElmer Lambda 950 spectrophotometer. Tauc plot with direct band gap assumption was used to obtain the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"DOI 10.1007/s12274-015-0948-y\",\n        \"dataset_ID\": 729,\n        \"id\": 238,\n        \"compound_name\": \"tris(methylammonium) bismuth iodide\",\n        \"formula\": \"C3H18N3Bi2I9\",\n        \"group\": \"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"tris(methanaminium) bismuth iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic\\u2013inorganic bismuth (III)-based material: A leadfree, air-stable and solution-processable light-absorber beyond organolead perovskites\",\n        \"journal\": \"Nano Research\",\n        \"vol\": \"9\",\n        \"pages_start\": \"692\",\n        \"pages_end\": \"702\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium iodide (MAI), bismuth iodide (BiI3), DMF (N,N-dimethylformamide), FTO covered with TiO2 mesoporous layers\",\n        \"synthesis_product\": \"Red ~500 nm thick film\",\n        \"synthesis_description\": \"0.2384 g of MAI and 0.5897 g of BiI3 were mixed in 1 mL of DMF. The solution was filtered using PTFE syringe filters (0.45 \\u03bcm) before use. 50 \\u03bcL of the solution was spin-coated at 4,000 rpm for 30 s with a ramp rate of 4,000 rpm\\u00b7s\\u20131. The film was heated at 100 \\u00b0C for 10 min on a hotplate.\",\n        \"experimental_method\": \"UV\\u2013vis absorption (reflectance)\",\n        \"experimental_description\": \"The absorption spectrum was recorded using Shimadzu UV2450. The band gap value was obtained by Tauc plot with an indirect band gap assumption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7TA06679A\",\n        \"dataset_ID\": 730,\n        \"id\": 207,\n        \"compound_name\": \"Tris(methylammonium) antimony iodide\",\n        \"formula\": \"C3H18N3Sb2I9\",\n        \"group\": \"MA3Sb2I9, (CH3NH3)3Sb2I9, tris(methanaminium) nonaiodo diantimonate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"Sb2I9, Antimony iodide\",\n        \"iupac\": \"tris(methanaminium) antimony iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Solution-processable antimony-based light-absorbing materials beyond lead halide perovskites\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"5\",\n        \"pages_start\": \"20843\",\n        \"pages_end\": \"20850\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"SbI3 (99.998%), methylamine (CH3NH2, 40 wt.% in water), dimethylformamide (DMF), Aqueous hydroiodic acid (HI) (57 wt.% in water)\",\n        \"synthesis_product\": \"orange MA2Sb2I9 film\",\n        \"synthesis_description\": \"SbI3 and MAI were dissolved in the DMF and heated at 70 \\u00b0C overnight. The heating was stopped and a specific volume of HI was added to it. The solution was spin-coated (6000 rpm) onto ITO/PEDOT:PSS substrates and was annealed at 70 \\u00b0C.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The absorption spectrum was measured using a Jacobs V-670 UV\\u2013Vis spectrophotometer\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 731,\n        \"id\": 208,\n        \"compound_name\": \"3-(aminomethyl)pyridinium lead iodide\",\n        \"formula\": \"C6H10N2PbI4\",\n        \"group\": \"(3AMPY)PbI4, (C6H10N2)PbI4, 3-(methanaminium)pyridinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, 3-(aminomethyl)pyridine (3AMPY), Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Red plate-like (3AMPY)PbI4 crystal\",\n        \"synthesis_description\": \"To a hot yellow solution of 0.5 mmol PbO in 2.5 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.5 mmol 3AMPY neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-like crystals precipitate upon cooling the above to 120\\u00b0C and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pn\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 732,\n        \"id\": 209,\n        \"compound_name\": \"3-(aminomethyl)pyridinium methylammonium lead iodide\",\n        \"formula\": \"C7H16N3Pb2I7\",\n        \"group\": \"(3AMPY)(MA)Pb2I7, (C7H16N3)Pb2I7, 3-(methanaminium)pyridinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium methanaminium lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, CH3NH3Cl, Aq. HI, Aq. H3PO2, 3-(aminomethyl)pyridine\",\n        \"synthesis_product\": \"Dark-red plate-like (3AMPY)(MA)Pb2I7 crystals\",\n        \"synthesis_description\": \"To a hot yellow solution of 2 mmol PbO and 1 mmol CH3NH3Cl in 2.75 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.7 mmol 3-(aminomethyl)pyridine (3AMPY) neutralized in 0.5 ml concentrated. Aq. H3PO2 was added under stirring. Dark red plate-shaped crystals precipitate upon cooling the above to 120\\u00b0C, and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 733,\n        \"id\": 210,\n        \"compound_name\": \"3-(aminomethyl)pyridinium bis(methylammonium) lead iodide\",\n        \"formula\": \"C8H22N4Pb3I10\",\n        \"group\": \"(3AMPY)(MA)2Pb3I10, (C8H22N4)Pb3I10, 3-(methanaminium)pyridinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H10N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, CH3NH3Cl, 3-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Black plate-like (3AMPY)(MA)2Pb3I10 crystals\",\n        \"synthesis_description\": \"To a hot yellow solution of 1.5 mmol PbO and 1 mmol CH3NH3Cl in 2.25 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.2 mmol 3-(aminomethyl)pyridine (3AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Black plate-shaped crystals precipitate upon cooling the above to 120\\u00b0C, and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 734,\n        \"id\": 211,\n        \"compound_name\": \"3-(aminomethyl)pyridinium tris(methylammonium) lead iodide\",\n        \"formula\": \"C9H28N5Pb4I13\",\n        \"group\": \"(3AMPY)(MA)3Pb4I13, (C9H28N5)Pb4I13, 3-(methanaminium)pyridinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H10N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, CH3NH3Cl, 3-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Black plate-like (3AMPY)(MA)3Pb4I13 crystals\",\n        \"synthesis_description\": \"To a hot yellow solution of 2 mmol PbO and 1.5 mmol CH3NH3Cl in 3.25 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.15 mmol 3-(aminomethyl)pyridine (3AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Black plate-shaped crystals precipitate upon cooling the above to 120\\u00b0C, and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 735,\n        \"id\": 212,\n        \"compound_name\": \"4-(aminomethyl)pyridinium lead iodide\",\n        \"formula\": \"C6H10N2PbI4\",\n        \"group\": \"(4AMPY)PbI4, (C6H10N2)PbI4, 4-(methanaminium)pyridinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Red plate-like (4AMPY)PbI4 crystals\",\n        \"synthesis_description\": \"To a hot yellow solution of 0.5 mmol PbO in 2 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.5 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.4 ml concentrated Aq. H3PO2 was added under stirring. Orange plate-shaped crystals precipitate upon cooling the above to 120\\u00b0C.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pn\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 736,\n        \"id\": 213,\n        \"compound_name\": \"4-(aminomethyl)pyridinium methylammonium lead iodide\",\n        \"formula\": \"C7H16N3Pb2I7\",\n        \"group\": \"(4AMPY)(MA)Pb2I7, (C7H16N3)Pb2I7, 4-(methanaminium)pyridinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium methanaminium lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, CH3NH3Cl, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Dark red plate-like (4AMPY)(MA)Pb2I7 crystals\",\n        \"synthesis_description\": \"To a hot yellow solution of 2 mmol PbO and 1 mmol CH3NH3Cl in 2.75 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.6 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-shaped crystals precipitate upon cooling the above to 120\\u00b0C, and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 737,\n        \"id\": 214,\n        \"compound_name\": \"4-(aminomethyl)pyridinium bis(methylammonium) lead iodide\",\n        \"formula\": \"C8H22N4Pb3I10\",\n        \"group\": \"(4AMPY)(MA)2Pb3I10, (C8H22N4)Pb3I10, 4-(methanaminium)pyridinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H10N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, CH3NH3Cl, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Black plate-like (4AMPY)(MA)2Pb3I10 crystals\",\n        \"synthesis_description\": \"To a hot yellow solution of 1.5 mmol PbO and 1 mmol CH3NH3Cl in 2.5 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.25 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Dark red plate-shaped crystals precipitate upon cooling the above to 120\\u00b0C, and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 738,\n        \"id\": 215,\n        \"compound_name\": \"4-(aminomethyl)pyridinium tris(methylammonium) lead iodide\",\n        \"formula\": \"C9H28N5Pb4I13\",\n        \"group\": \"(4AMPY)(MA)3Pb4I13, (C9H28N5)Pb4I13, 4-(methanaminium)pyridinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H10N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, CH3NH3Cl, 4-(aminomethyl)pyridine, Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Black (4AMPY)(MA)3Pb4I13 crystals\",\n        \"synthesis_description\": \"To a hot yellow solution of 2 mmol PbO and 1.5 mmol CH3NH3Cl in 3.25 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.14 mmol 4-(aminomethyl)pyridine (4AMPY) neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Black plate-shaped crystals precipitate upon cooling the above to 120\\u00b0C, and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ic\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 744,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"PBE with Tkatchenko-Scheffler van der Waals correction\",\n        \"k_point_grid\": \"1x2x2\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"tight\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/d1nr06899g\",\n        \"dataset_ID\": 745,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            225,\n            1901,\n            1903,\n            2267,\n            2269\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2*8*8\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"On the optical anisotropy in 2D metal-halide perovskites\",\n        \"journal\": \"Nanoscale\",\n        \"vol\": \"14\",\n        \"pages_start\": \"752\",\n        \"pages_end\": \"765\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.9b11809\",\n        \"dataset_ID\": 746,\n        \"id\": 217,\n        \"compound_name\": \"Bis(benzylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"bis(benzylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Control of Crystal Symmetry Breaking with Halogen-Substituted Benzylammonium in Layered Hybrid Metal-Halide Perovskites\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"142\",\n        \"pages_start\": \"5060\",\n        \"pages_end\": \"5067\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Benzylamine (BzA), PbI2, Aq. HI (57%), H3PO2 (50 %)\",\n        \"synthesis_product\": \"Orange (BzA)2PbI4 crystals\",\n        \"synthesis_description\": \"BzA (214.45 mg) was dissolved in Aq.HI (4.5 ml) treated with hypophosphorous acid (0.5 ml) as a stabilizer. A stoichiometric amount of PbI2 (461.01) was added to the above solution, stirred at 90 \\u00b0C for 2 h, and cooled to room temperature at a rate of 1 K/hr to induce crystallization. All synthesis was performed at ambient conditions. The as-formed crystals were collected by suction, washed with diethyl ether and dried under vacuum.\",\n        \"experimental_method\": \"single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray data were collected on a Nonius Kappa CCD single-crystal diffractometer (MoK\\u03b1, \\u03bb = 0.71073 \\u00c5) at 180 K.\",\n        \"physical_property\": \"180.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 763,\n        \"id\": 218,\n        \"compound_name\": \"Bis(ethylammoniumbithiophene) lead iodide\",\n        \"formula\": \"C20H24N2S4PbI4\",\n        \"group\": \"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",\n        \"organic\": \"C10H12NS2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            777\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. 2T (100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film forms after the solvent dry off.\",\n        \"experimental_method\": \"Steady-state Photoluminescence\",\n        \"experimental_description\": \"A home-built confocal micro-photoluminescence setup was used to record the PL spectrum.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 777,\n        \"id\": 218,\n        \"compound_name\": \"Bis(ethylammoniumbithiophene) lead iodide\",\n        \"formula\": \"C20H24N2S4PbI4\",\n        \"group\": \"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",\n        \"organic\": \"C10H12NS2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            763\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. 2T (100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film forms after the solvent dry off.\",\n        \"experimental_method\": \"Steady-state Photoluminescence\",\n        \"experimental_description\": \"A home-built confocal micro-photoluminescence setup was used to record the PL spectrum.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 786,\n        \"id\": 219,\n        \"compound_name\": \"Bis(ethylammoniumdimethylquaterthiophene) lead iodide\",\n        \"formula\": \"C40H40N2S8PbI4\",\n        \"group\": \"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) \\u00ac\\u2211I3Pb\\u00ac\\u2211I, 5-ethanaminium-4',3'''dimethyl-2,2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2-quaterthiophene tetraiodoplumbate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5-ethanaminium-4',3'''dimethyl-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 4Tm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 4Tm (10.6 mg, 20  \\u00b5mol) and PbI2(4.6 mg, 10 \\u00b5mol) were dissolved in a mixture of DMF (1 mL) and CB (1 mL). \\r\\nTo obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",\n        \"experimental_method\": \"Single Crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Data were collected using a Bruker AXS D8 Quest CMOS diffractometer, an I-mu-S microsource X-ray tube with Cu K\\u03b1 radiation (\\u03bb = 1.54178 \\u00c5), Goebel mirror, and a Photon2 CMOS area detector. Data was collected and analyzed at 150 K. Files were scaled and corrected using APEX3.\",\n        \"physical_property\": \"150.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 788,\n        \"id\": 219,\n        \"compound_name\": \"Bis(ethylammoniumdimethylquaterthiophene) lead iodide\",\n        \"formula\": \"C40H40N2S8PbI4\",\n        \"group\": \"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) \\u00ac\\u2211I3Pb\\u00ac\\u2211I, 5-ethanaminium-4',3'''dimethyl-2,2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2-quaterthiophene tetraiodoplumbate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5-ethanaminium-4',3'''dimethyl-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 4Tm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2\",\n        \"synthesis_product\": \"orange crystals\",\n        \"synthesis_description\": \"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 4Tm (10.6 mg, 20 \\u00b5mol) and PbI2(4.6 mg, 10 \\u00b5mol) were dissolved in a mixture of DMF (1 mL) and CB (1 mL). Afterward, the solution was diluted 60 times with acetonitrile/chlorobenzene (1:2:5 volume ratio). The solution was diluted 5 more times with either CB or CB/acetonitrile (3:1 volume ratio). Next, the Si/SiO2 substrates were then cleaned via ultrasonication in isopropanol, water, acetone, and isopropanol again. Substrates were dried by a nitrogen gun, transported into the glove box, and preheated to 80\\u00ba C. The prepared, diluted solution was then dropped onto the Si/SiO2 substrate, 10 mL at a time, and dried at 80\\u00baC. Thin sheets of (4Tm)2PbI4 grew spontaneously within 10 minutes. To obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",\n        \"experimental_method\": \"Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.\",\n        \"experimental_description\": \"Absorption correction was performed with Multi-scan SADABS 2016/2: Krause, L., Herbst-Irmer, R., Sheldrick G.M. & Stalke D., J. Appl. Cryst. 48 (2015) 3-10.\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 794,\n        \"id\": 219,\n        \"compound_name\": \"Bis(ethylammoniumdimethylquaterthiophene) lead iodide\",\n        \"formula\": \"C40H40N2S8PbI4\",\n        \"group\": \"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) \\u00ac\\u2211I3Pb\\u00ac\\u2211I, 5-ethanaminium-4',3'''dimethyl-2,2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2-quaterthiophene tetraiodoplumbate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5-ethanaminium-4',3'''dimethyl-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (band edge difference)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 4Tm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. 4Tm (53.0 mg, 100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed at 200 \\u00b0C on a hot plate for 10 min.\",\n        \"experimental_method\": \"Ultraviolet photoelectron spectroscopy (UPS) + Cyclic voltametry (CV)\",\n        \"experimental_description\": \"UPS was recorded using Kratos Axis Ultra DLD spectrometer with He I radiation (21.2 eV) at pass energy (PE) of 5 eV. CV was recorded using a CHI660 electrochemical analyzer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 795,\n        \"id\": 218,\n        \"compound_name\": \"Bis(ethylammoniumbithiophene) lead iodide\",\n        \"formula\": \"C20H24N2S4PbI4\",\n        \"group\": \"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",\n        \"organic\": \"C10H12NS2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. 2T (100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film forms after the solvent dry off.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 798,\n        \"id\": 220,\n        \"compound_name\": \"Bis(ethylammoniumdimethylquaterthiophenecarbonitrile) lead iodide\",\n        \"formula\": \"C40H36N6S8PbI4\",\n        \"group\": \"(4TCNm)2PbI4, (C20H18N3S4)2PbI4, 5-ethanaminium-4',3'''dimethyl-2,2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2-quaterthiophene-3'',4''-dicarbonitrile tetraiodoplumbate(II) \",\n        \"organic\": \"C20H18N3S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5-ethanaminium-4',3'''dimethyl-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene-3'',4''-dicarbonitrile\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (band edge difference)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 4TCNm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. 4TCNm (100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed at 180 \\u00b0C on a hot plate for 10 min.\",\n        \"experimental_method\": \"Ultraviolet photoelectron spectroscopy (UPS) + Cyclic voltametry (CV)\",\n        \"experimental_description\": \"UPS was recorded using Kratos Axis Ultra DLD spectrometer with He I radiation (21.2 eV) at pass energy (PE) of 5 eV. CV was recorded using a CHI660 electrochemical analyzer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 799,\n        \"id\": 220,\n        \"compound_name\": \"Bis(ethylammoniumdimethylquaterthiophenecarbonitrile) lead iodide\",\n        \"formula\": \"C40H36N6S8PbI4\",\n        \"group\": \"(4TCNm)2PbI4, (C20H18N3S4)2PbI4, 5-ethanaminium-4',3'''dimethyl-2,2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2-quaterthiophene-3'',4''-dicarbonitrile tetraiodoplumbate(II) \",\n        \"organic\": \"C20H18N3S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5-ethanaminium-4',3'''dimethyl-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene-3'',4''-dicarbonitrile\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 4TCNm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2\",\n        \"synthesis_product\": \"Yellow solid\",\n        \"synthesis_description\": \"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 4TCNm (10.6 mg, 20 \\u00b5mol) and PbI2(4.6 mg, 10 \\u00b5mol) were dissolved in a mixture of DMF (1 mL) and CB (1 mL). Afterward, the solution was diluted 60 times with acetonitrile/chlorobenzene (1:2:5 volume ratio). The solution was diluted 5 more times with either CB or CB/acetonitrile (3:1 volume ratio). Next, the Si/SiO2 substrates were then cleaned via ultrasonication in isopropanol, water, acetone, and isopropanol again. Substrates were dried by a nitrogen gun, transported into the glove box, and preheated to 80\\u00ba C. The prepared, diluted solution was then dropped onto the Si/SiO2 substrate, 10 mL at a time, and dried at 80\\u00baC. Thin sheets of (4TCNm)2PbI4 grew spontaneously within 10 minutes. Thin polycrystalline films were annealed at 100\\u00ba. Though the organic ligand was too large (and approaching the extent of the perovskite\\u2019s lattice), a yellow solid product resulted.\",\n        \"experimental_method\": \"Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.\",\n        \"experimental_description\": \"Absorption correction was performed with Multi-scan SADABS 2016/2: Krause, L., Herbst-Irmer, R., Sheldrick G.M. & Stalke D., J. Appl. Cryst. 48 (2015) 3-10.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 801,\n        \"id\": 221,\n        \"compound_name\": \"bis(BTm) lead iodide\",\n        \"formula\": \"C24H22NS4PbI4\",\n        \"group\": \"(BTm)2PbI4, I8Pb2\\u00ac\\u22114(C24H22NS4), (BTm)2PbI4\",\n        \"organic\": \"C24H22NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"There is an erratum reported for this publication. However, the data listed here was and is correct.\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (band edge difference)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. BTm (100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed on a hot plate for 10 min.\",\n        \"experimental_method\": \"Ultraviolet photoelectron spectroscopy (UPS) + Cyclic voltametry (CV)\",\n        \"experimental_description\": \"UPS was recorded using Kratos Axis Ultra DLD spectrometer with He I radiation (21.2 eV) at pass energy (PE) of 5 eV. CV was recorded using a CHI660 electrochemical analyzer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 802,\n        \"id\": 221,\n        \"compound_name\": \"bis(BTm) lead iodide\",\n        \"formula\": \"C24H22NS4PbI4\",\n        \"group\": \"(BTm)2PbI4, I8Pb2\\u00ac\\u22114(C24H22NS4), (BTm)2PbI4\",\n        \"organic\": \"C24H22NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"There is an erratum reported for this publication. However, the data listed here was and is correct.\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. BTm (100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed on a hot plate for 10 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Absorption spectra was obtained by using an Agilent UV-Vis-NIR Cary-5000 spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 803,\n        \"id\": 221,\n        \"compound_name\": \"bis(BTm) lead iodide\",\n        \"formula\": \"C24H22NS4PbI4\",\n        \"group\": \"(BTm)2PbI4, I8Pb2\\u00ac\\u22114(C24H22NS4), (BTm)2PbI4\",\n        \"organic\": \"C24H22NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"There is an erratum reported for this publication. However, the data listed here was and is correct.\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl), Si/SiO2 wafer\",\n        \"synthesis_product\": \"Thin film\",\n        \"synthesis_description\": \"The entire procedure was performed inside a nitrogen-filled glove box. BTm (100 \\u03bcmol) and PbI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 0.25 mL of anhydrous DMF at 70 \\u00b0C. The cooled DMF solution was spin-coated at 2000 rpm for 60 s. The film was annealed on a hot plate for 10 min.\",\n        \"experimental_method\": \"Steady-state Photoluminescence\",\n        \"experimental_description\": \"A home-built confocal micro-photoluminescence setup was used to record the PL spectrum.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 804,\n        \"id\": 221,\n        \"compound_name\": \"bis(BTm) lead iodide\",\n        \"formula\": \"C24H22NS4PbI4\",\n        \"group\": \"(BTm)2PbI4, I8Pb2\\u00ac\\u22114(C24H22NS4), (BTm)2PbI4\",\n        \"organic\": \"C24H22NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(4'-methyl-5'-(7-(3-methylthiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)-[2,2'-bithiophen]-5-yl)ethan-1-aminium lead (II) iodide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"There is an erratum reported for this publication. However, the data listed here was and is correct.\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized BTm, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl)\",\n        \"synthesis_product\": \"red plates\",\n        \"synthesis_description\": \"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized BTm (10.6 mg, 20  \\u00b5mol) and PbI2(4.6 mg, 10 \\u00b5mol) were dissolved in a mixture of DMF (1 mL). To obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",\n        \"experimental_method\": \"Single Crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Data were collected using a Bruker AXS D8 Quest CMOS diffractometer with PhotonII charge-integrating pixel array detector (CPAD), an I-\\u00b5-S microsource X-ray tube (Cu K???? radiation, ????=1.54178 \\u00c5), Goebel mirror, and a Photon2 CMOS area detector. Data was collected and analyzed at 150 K. Files were scaled and corrected using APEX3.\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P(-1)\",\n        \"extraction_method\": \"Extracted manually from article\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-019-0354-2\",\n        \"dataset_ID\": 805,\n        \"id\": 218,\n        \"compound_name\": \"Bis(ethylammoniumbithiophene) lead iodide\",\n        \"formula\": \"C20H24N2S4PbI4\",\n        \"group\": \"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",\n        \"organic\": \"C10H12NS2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular engineering of organic-inorganic hybrid perovskites quantum wells\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1151\",\n        \"pages_end\": \"1157\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"As-synthesized 2T, PbI2, anhydrous dimethyl formamide (DMF) ((CH3)2NCH), anhydrous chlorobenzene (CB) (C6H5Cl)\",\n        \"synthesis_product\": \"orange-red plates\",\n        \"synthesis_description\": \"Solution and thin film growth experiments were prepared and executed inside of a nitrogen-filled glove box with oxygen and water levels less than 1 ppm. Inside a 4 mL vial, as-synthesized 2T (10.6 mg, 20  \\u00b5mol) and PbI2(4.6 mg, 10 \\u00b5mol) were dissolved in a mixture of DMF (1 mL).\\r\\n\\r\\nTo obtain single crystals, the solution in DMF was diffused with chloroform and chlorobenzene vapor. This resulted in thin orange-red plates.\",\n        \"experimental_method\": \"Single Crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Data was collected via a Bruker AXS D8 Quest diffractometer, a sealed tube X-ray radiation source with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), and a triumph curved graphite crystal monochromator. Data was collected and analyzed at 150 K. Files were scaled and corrected using APEX3.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 806,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\n        \"synthesis_product\": \"thin, yellow-green plates\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",\n        \"experimental_method\": \"Single-crystal X-Ray diffraction\",\n        \"experimental_description\": \"The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 \\u00c5 (16 keV) radiation.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pccn\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 807,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\n        \"synthesis_product\": \"thin, yellow-green plates\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",\n        \"experimental_method\": \"Single-crystal X-Ray diffraction\",\n        \"experimental_description\": \"The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 \\u00c5 (16 keV) radiation.\",\n        \"physical_property\": \"350.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pccn\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 808,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\n        \"synthesis_product\": \"thin, yellow-green plates\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",\n        \"experimental_method\": \"Single-crystal X-Ray diffraction\",\n        \"experimental_description\": \"The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 \\u00c5 (16 keV) radiation.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pccn\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 809,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-MHCl\",\n        \"synthesis_product\": \"thin, yellow-green plates\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours. To obtain the crystals for analysis, a 1 mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (0.054 mL, 0.37 mmol) in acetonitrile was placed at the bottom of a 4-mL vial, and 12-M HCl (0.062 mL) was poured on top. The mixture to separate into layers, and a 1-mL methanol solution of CuCl2 (0.05 g, 0.37 mmol) was added slowly on top. Thin yellow-green plates were formed after 48 hours, and the plates were washed with diethyl ether.\",\n        \"experimental_method\": \"Single-crystal X-Ray diffraction\",\n        \"experimental_description\": \"The data were collected at beamlines 11.3.1 of the Advanced Light Source (ALS). Single-crystal measurements were conducted using 0.7749 \\u00c5 (16 keV) radiation.\",\n        \"physical_property\": \"200.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pccn\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 815,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",\n        \"synthesis_product\": \"yellow-green powder\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at reduced temperature for 12 hours.\",\n        \"experimental_method\": \"High-pressure optical absorption\",\n        \"experimental_description\": \"The data were collected at the beamline U2A of the National Synchrotron Light Source (NSLS) at Brookhaven National Laboratory (BNL). Tauc plot with direct band gap assumption was used to obtain the band gap value.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.5b13294\",\n        \"dataset_ID\": 821,\n        \"id\": 223,\n        \"compound_name\": \"Cesium silver bismuth bromide\",\n        \"formula\": \"Cs2AgBiBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Bismuth-Halide Double Perovskite with Long Carrier Recombination Lifetime for Photovoltaic Applications\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2138\",\n        \"pages_end\": \"2141\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",\n        \"synthesis_product\": \"red-orange crystals\",\n        \"synthesis_description\": \"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110\\u00ba C for 2 hours, and cooled to room temperature by controlling the cooling rate to 2\\u00baC/hr or 1\\u00baC/hr. The obtained crystals were filtered on a glass frit and dried under low pressure overnight.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"A crystal was coated in Paratone-N oil, placed on a Kapton loop, and transferred to a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector. Data was collected using \\u03c9v and \\u03c8 scans with 18-keV synchrotron radiation (\\u03bb = 0.68880 \\u00c5)\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.5b13294\",\n        \"dataset_ID\": 823,\n        \"id\": 223,\n        \"compound_name\": \"Cesium silver bismuth bromide\",\n        \"formula\": \"Cs2AgBiBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            824\n        ],\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Bismuth-Halide Double Perovskite with Long Carrier Recombination Lifetime for Photovoltaic Applications\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2138\",\n        \"pages_end\": \"2141\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",\n        \"synthesis_product\": \"orange powder\",\n        \"synthesis_description\": \"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterwards, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110\\u00ba C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",\n        \"experimental_method\": \"Estimation through Tauc plot.\",\n        \"experimental_description\": \"Cary 6000i UV-Vis spectrometer equipped with an integrating sphere was used in absorbance mode to collect absorption data. The powder was pressed and mounted on a quartz slide such that incident light was normal to the surface.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.5b13294\",\n        \"dataset_ID\": 824,\n        \"id\": 223,\n        \"compound_name\": \"Cesium silver bismuth bromide\",\n        \"formula\": \"Cs2AgBiBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            823\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"abs. units\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Bismuth-Halide Double Perovskite with Long Carrier Recombination Lifetime for Photovoltaic Applications\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2138\",\n        \"pages_end\": \"2141\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",\n        \"synthesis_product\": \"orange powder\",\n        \"synthesis_description\": \"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110\\u00ba C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Cary 6000i UV-Vis spectrometer equipped with an integrating sphere was used in absorbance mode to collect absorption data. The powder was pressed and mounted on a quartz slide such that incident light was normal to the surface.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.5b13294\",\n        \"dataset_ID\": 825,\n        \"id\": 223,\n        \"compound_name\": \"Cesium silver bismuth bromide\",\n        \"formula\": \"Cs2AgBiBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Bismuth-Halide Double Perovskite with Long Carrier Recombination Lifetime for Photovoltaic Applications\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2138\",\n        \"pages_end\": \"2141\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",\n        \"synthesis_product\": \"orange powder\",\n        \"synthesis_description\": \"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110\\u00ba C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Room-temperature steady-state emission spectra were collected on powders mounted on quartz slides using a Horiba Jobin-Yvon Spex Fluorolog-3 fluorimeter equipped with a 450-W xenon lamp and a thermoelectrically-cooled R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b01336\",\n        \"dataset_ID\": 826,\n        \"id\": 224,\n        \"compound_name\": \"Bis(4-fluorophenethylammonium) lead iodide\",\n        \"formula\": \"C16H22N2F2PbI4\",\n        \"group\": \"(FPEA)2PbI4,  4-FC6H4(CH2)2NH3+)PbI4, bis(4-fluorophenethanaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C8H11NF\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(4-fluorophenethanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Chemical Approaches to Addressing the Instability and Toxicity of Lead-Halide Perovskite Absorbers\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"46\",\n        \"pages_end\": \"55\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetone, nitromethane, NaI\",\n        \"synthesis_product\": \"orange, plate-shaped crystals\",\n        \"synthesis_description\": \"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0\\u00ba C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60\\u00ba  C, saturated isopropanol solution was cooled to -10\\u00ba C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (12 mg, 0.043 mmol) and PbI2 (10 mg, 0.022 mmol) in acetone (10 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added and orange, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",\n        \"experimental_method\": \"Single crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.7749 \\u00c5.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b01336\",\n        \"dataset_ID\": 828,\n        \"id\": 225,\n        \"compound_name\": \"Bis(4-fluorophenethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C17H28N3F2Pb2I7\",\n        \"group\": \"(FPEA)2(MA)Pb2I7, (4-FC6H4(CH2)2NH3+)Pb2I7, bis(4-fluorophenethanaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C8H11NF, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(4-fluorophenethanaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-06-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Chemical Approaches to Addressing the Instability and Toxicity of Lead-Halide Perovskite Absorbers\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"46\",\n        \"pages_end\": \"55\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetone, nitromethane, NaI, methylammonium iodide (MAI)\",\n        \"synthesis_product\": \"light red, plate-shaped crystals\",\n        \"synthesis_description\": \"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0\\u00ba C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60\\u00ba  C, saturated isopropanol solution was cooled to -10\\u00ba C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (5.8 mg, 0.022 mmol), (MA)I (1.7 mg, 0.011 mmol), and PbI2 (10 mg, 0.022 mmol) in acetone (10 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added and light red, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",\n        \"experimental_method\": \"Single crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.6888 \\u00c5.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b01336\",\n        \"dataset_ID\": 830,\n        \"id\": 226,\n        \"compound_name\": \"Bis(4-fluorophenethylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C18H34N4F2Pb3I10\",\n        \"group\": \"(FPEA)2(MA)2Pb3I10, (4-FC6H4(CH2)2NH3+)2(CH3NH3)2Pb3I10, bis(4-fluorophenethanaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C8H11NF, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(4-fluorophenethanaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Chemical Approaches to Addressing the Instability and Toxicity of Lead-Halide Perovskite Absorbers\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"46\",\n        \"pages_end\": \"55\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetonitrile, nitromethane, NaI, methylammonium iodide (MAI)\",\n        \"synthesis_product\": \"dark red, plate-shaped crystals\",\n        \"synthesis_description\": \"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0\\u00ba C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60\\u00ba  C, saturated isopropanol solution was cooled to -10\\u00ba C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (3.9 mg, 0.014 mmol), (MA)I (2.3 mg, 0.014 mmol), and PbI2 (10 mg, 0.022 mmol) in acetonitrile (8 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added, and dark red, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",\n        \"experimental_method\": \"Single crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.7749 \\u00c5.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b01336\",\n        \"dataset_ID\": 831,\n        \"id\": 226,\n        \"compound_name\": \"Bis(4-fluorophenethylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C18H34N4F2Pb3I10\",\n        \"group\": \"(FPEA)2(MA)2Pb3I10, (4-FC6H4(CH2)2NH3+)2(CH3NH3)2Pb3I10, bis(4-fluorophenethanaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C8H11NF, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(4-fluorophenethanaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Chemical Approaches to Addressing the Instability and Toxicity of Lead-Halide Perovskite Absorbers\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"46\",\n        \"pages_end\": \"55\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (55-57% w/w containing 1.5% hypophosphorous acid as stabilizer), 4-fluorophenethylamine, PbI2, acetonitrile, nitromethane, NaI, methylammonium iodide (MAI)\",\n        \"synthesis_product\": \"dark red, plate-shaped crystals\",\n        \"synthesis_description\": \"(FPEA)I was first synthesized by adding concentrated hydroiodic acid (2.4 mL) to 4-fluorphenethylamine (2.0 mL) at 0\\u00ba C. A colorless precipitate formed, and the solid was filtered and washed with dethyl ether. A 60\\u00ba  C, saturated isopropanol solution was cooled to -10\\u00ba C and (FPEA)I resulted. The perovskite crystals were formed by dissolving solid (FPEA)I (3.9 mg, 0.014 mmol), (MA)I (2.3 mg, 0.014 mmol), and PbI2 (10 mg, 0.022 mmol) in acetonitrile (8 mL) and nitromethane (5mL). To enhance solubility, solid NaI (6.5 mg, 0.043 mmol) was added and dark red, plate-shaped crystals formed over 6 days from slow solvent evaporation.\",\n        \"experimental_method\": \"Single crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Conducted on Beamline 11.3.1. Crystals were coated with Paratone-N oil, placed on a MiTeGen sample mount, and then mounted on the goniometer head of Bruker d85 diffractometer with Photon 100 CMOS detector. Data were corrected for Lorentz and polarization effects via SAINT v8.34A and for absorption effects via TWINABS V2012/I4. The incident radiation was 0.7749 \\u00c5.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja206171\",\n        \"dataset_ID\": 834,\n        \"id\": 227,\n        \"compound_name\": \"methylviologen BiI3Cl2\",\n        \"formula\": \"(MV)BiI3Cl2\",\n        \"group\": \"Methylviologen dichloro triiodo bismuthate(III)\",\n        \"organic\": \"C12H14N2\",\n        \"inorganic\": \"BiI3Cl2, Bismuth chloride iodide\",\n        \"iupac\": \"1,1\\u2032-Dimethyl-4,4\\u2032-bipyridinium bismuth triiodide dichloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"The structure of (MV)BiI3Cl2 can be described as [BiI3Cl2] chains of trans-connected octahedra separated by methylviologen dications, defining a chessboard arrangement when viewed along the chains.\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Large Spontaneous Polarization and Clear Hysteresis Loop of a Room-Temperature Hybrid Ferroelectric Based on Mixed-Halide [BiI3Cl2] Polar Chains and Methylviologen Dication\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"133\",\n        \"pages_start\": \"14924\",\n        \"pages_end\": \"14927\",\n        \"year\": \"2011\",\n        \"synthesis_starting_materials\": \"BiCl3, 4,40-bipyridine, concentrated HCl and HI in methanol\",\n        \"synthesis_product\": \"(MV)[BiI3Cl2] single crystal with face sizes up to 0.4 mm\",\n        \"synthesis_description\": \"Mix 0.4 mmol of BiCl3, 0.4 mmol of 4,40-bipyridine, 10 mL of MeOH, 1,7 mL of HCl (36%), and 0.1 mL of HI (57%) in a 25 mL Teflon bomb. Seal bomb in a Parr autoclave and heat in a programmable oven with the following parameters: heat from 25 to 150 \\u00b0\\u0001C over 2 h, hold at 150 \\u0001\\u00b0C for 13 h, and then cool to 25 \\u00b0\\u0001C over 10 h. A mixture of dark (MV)[BiI3Cl2] crystals and yellow (MV)4[Bi6Cl26] crystals in a ratio of \\u223c9:1 grew. Collect by filtration and wash with methanol.\",\n        \"experimental_method\": \"X-ray diffraction\",\n        \"experimental_description\": \"Collected on a Bruker-Nonius Kappa-CDD diffractometer equipped with graphite monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6sc02848a\",\n        \"dataset_ID\": 835,\n        \"id\": 228,\n        \"compound_name\": \"bis(6-Iodohexylammonium) lead iodide\",\n        \"formula\": \"C12H30N2I2PbI4\",\n        \"group\": \"(IC6)2[PbI4], C12H30N2PbI6, bis(1-iodohexyl-6-aminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H15NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(1-iodohexyl-6-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Decreasing the electronic confinement in layered perovskites through intercalation\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"1960\",\n        \"pages_end\": \"1968\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbI2, 6-amino-1-hexanol, hydroiodic acid\",\n        \"synthesis_product\": \"red-orange crystals\",\n        \"synthesis_description\": \"solid PbI2 (0.455 g, 0.987 mmol) and 6-amino-1-hexanol (0.272 g, 2.32 mmol) were dissolved in concentrated hydroiodic acid (2 mL). The solution was sonicated for 5 minutes and resulted in a yellow-orange solution. The colored solution was heated at 100\\u00ba C for 3 hours and cooled to room temperature. This resulted in red-orange crystals that were filtered in glass frit and washed with diethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"To determine the crystal structure, a crystal was coated in Paratone-N oil, mounted to a Mitegen loop/micromesh mount, and transferred to a Bruker D8 Venture diffractometer with Photon 100 CMOS detector.\",\n        \"physical_property\": \"298.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6sc02848a\",\n        \"dataset_ID\": 837,\n        \"id\": 228,\n        \"compound_name\": \"bis(6-Iodohexylammonium) lead iodide\",\n        \"formula\": \"C12H30N2I2PbI4\",\n        \"group\": \"(IC6)2[PbI4], C12H30N2PbI6, bis(1-iodohexyl-6-aminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H15NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(1-iodohexyl-6-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"Structure optimized with GGA + vdW, Electronic property with HSE+SOC\",\n        \"k_point_grid\": \"4x4x1 (Monkhort-Pack)\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Decreasing the electronic confinement in layered perovskites through intercalation\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"1960\",\n        \"pages_end\": \"1968\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6sc02848a\",\n        \"dataset_ID\": 841,\n        \"id\": 228,\n        \"compound_name\": \"bis(6-Iodohexylammonium) lead iodide\",\n        \"formula\": \"C12H30N2I2PbI4\",\n        \"group\": \"(IC6)2[PbI4], C12H30N2PbI6, bis(1-iodohexyl-6-aminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H15NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(1-iodohexyl-6-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Decreasing the electronic confinement in layered perovskites through intercalation\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"1960\",\n        \"pages_end\": \"1968\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbI2, 6-amino-1-hexanol, hydroiodic acid, DMF\",\n        \"synthesis_product\": \"230 - 270 nm thick film\",\n        \"synthesis_description\": \"solid PbI2 (0.455 g, 0.987 mmol) and 6-amino-1-hexanol (0.272 g, 2.32 mmol) were dissolved in concentrated hydroiodic acid (2 mL). The solution was sonicated for 5 minutes and resulted in a yellow-orange solution. The colored solution was heated at 100\\u00ba C for 3 hours and cooled to room temperature. This resulted in red-orange crystals that were filtered in glass frit and washed with diethyl ether. The crystals were dissolved in DMF to prepare a 0.4 M solution. The solution was filtered through 0.22-\\u03bcm pore size Teflon syringe filters. 50-100 \\u03bcL of the solution was spun on quartz substrates at 3000 rpm for 50 s and then at 5000 rpm for 10 s. The films were annealed at 100 \\u00b0C for 10 minutes.\",\n        \"experimental_method\": \"Uv-vis absorption\",\n        \"experimental_description\": \"Data were recorded with an Agilent Cary 6000i spectrometer.\",\n        \"physical_property\": \"5.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsomega.8b02877\",\n        \"dataset_ID\": 842,\n        \"id\": 229,\n        \"compound_name\": \"tetrakis((R)-1-phenylethylammonium) bismuth bromide\",\n        \"formula\": \"C32H48N4Bi2Br10\",\n        \"group\": \"(R)-(MBA)4[BiBr10], (R)-1-phenylethylammonium bromobismuthate(III), [((R)-C8H12N)4][Bi2Br10]\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Bi2Br10, Bismuth bromide\",\n        \"iupac\": \"tetrakis((R)-1-phenylethylammonium) bismuth bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            843\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[((R)\\u2011C8H12N)4][Bi2Br10] and [((S)\\u2011C8H12N)4][Bi2Br10]: Chiral Hybrid Bismuth Bromides Templated by Chiral Organic Cations\",\n        \"journal\": \"ACS Omega\",\n        \"vol\": \"3\",\n        \"pages_start\": \"17895\",\n        \"pages_end\": \"17903\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"(R)-(+)-1-Phenylethylamine ((R)-1-PEA,  >99%), N,N\\u2032-dimethylformamide (DMF, anhydrous, 99.9%), bismuth-(III) bromide (BiBr3, 99.9%), and hydrobromic acid (HBr, 48 wt %)\",\n        \"synthesis_product\": \"Yellow large plate-like crystals\",\n        \"synthesis_description\": \"[((R)-C8H12N)4]-[Bi2Br10][(R)-1] was grown through a slow evaporation method. BiBr3 (0.8 x 10^{\\u22123} mol, 0.359 g) and (R)-1- phenylethylamine (1.6 x 10^{\\u22123} mol, 0.206 mL) were dissolved in 6 mL of a 48% HBr aqueous solution. The solution mixture was heated at 60 \\u00b0C for 20 min and slowly cooled to room temperature. Yellow crystals of compounds (R)-1 were grown in 2 days as the solvent slowly evaporated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were recorded using Bruker SMART BREEZE diffractometer on graphite-monochromated Mo-K\\u03b1 radiation (\\u03bb 0.71073 \\u00c5) and a 1 K charge-coupled device (CCD) area detector at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsomega.8b02877\",\n        \"dataset_ID\": 843,\n        \"id\": 230,\n        \"compound_name\": \"tetrakis((S)-1-phenylethylammonium) bismuth bromide\",\n        \"formula\": \"C32H48N4Bi2Br10\",\n        \"group\": \"(S)-(MBA)4[BiBr10], (S)-1-phenylethylammonium bromobismuthate(III), [((S)-C8H12N)4][Bi2Br10]\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Bi2Br10, Bismuth bromide\",\n        \"iupac\": \"tetrakis((S)-1-phenylethylammonium) bismuth bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            842\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[((R)\\u2011C8H12N)4][Bi2Br10] and [((S)\\u2011C8H12N)4][Bi2Br10]: Chiral Hybrid Bismuth Bromides Templated by Chiral Organic Cations\",\n        \"journal\": \"ACS Omega\",\n        \"vol\": \"3\",\n        \"pages_start\": \"17895\",\n        \"pages_end\": \"17903\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-1-phenylethylamine ((S)-1-PEA, >99%), N,N\\u2032-dimethylformamide (DMF, anhydrous, 99.9%), bismuth-(III) bromide (BiBr3, 99.9%), and hydrobromic acid (HBr, 48 wt %)\",\n        \"synthesis_product\": \"Yellow large plate-like crystals\",\n        \"synthesis_description\": \"[((S)-C8H12N)4]-[Bi2Br10][(S)-1] was grown through a slow evaporation method. BiBr3 (0.8 x 10^{\\u22123} mol, 0.359 g) and (S)-1- phenylethylamine (1.6 x 10^{\\u22123} mol, 0.206 mL) were dissolved in 6 mL of a 48% HBr aqueous solution. The solution mixture was heated at 60 \\u00b0C for 20 min and slowly cooled to room temperature. Yellow crystals of compounds (S)-1 were grown in 2 days as the solvent slowly evaporated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using ADSC Quantum-210 CCD diffractometer with synchrotron radiation (\\u03bb = 0.63000 \\u00c5) at two-dimensional supramolecular crystallography at the Pohang Accelerator Laboratory, Korea.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 847,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbCl4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbCl4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbCl4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbCl4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbCl4 films at 150 \\u00b0C for 5 min.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Absorption spectra were obtained at room temperature on the thermally ablated films using a Hewlett-Packard UV-vis 8543 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 848,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbBr4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbBr4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbBr4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbBr4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbBr4 films at 180 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Absorption spectra were obtained at room temperature on the thermally ablated films using a Hewlett-Packard UV-vis 8543 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 849,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbI4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbI4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbI4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbI4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbI4 films at 200 \\u00b0C for 30 min.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Absorption spectra were obtained at room temperature on the thermally ablated films using a Hewlett-Packard UV-vis 8543 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 850,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"AEQT.2HBr, PbBr2, ethylene glycol, HBr (aq)\",\n        \"synthesis_product\": \"(AEQT)PbBr4 crystals\",\n        \"synthesis_description\": \"Prepare the starting AEQT.2HBr salt using a technique similar to that described in detail for the synthesis of AMQT.2HCl [1]. \\r\\n\\r\\nGrow (AEQT)PbBr4 crystals from a slowly cooled, saturated, aqueous solution containing the organic and inorganic salts. First, weigh 14.5 mg (0.025 mmol) of AEQT.2HBr and 18.3 mg (0.050 mmol) of PbBr2 and add to a test tube under an inert atmosphere. Dissolve the contents in the sealed tube at 120 \\u00b0C in a solvent mixture of 22 mL of deionized water, 1 mL of ethylene glycol, and 2 drops of 48% aqueous HBr, forming a nominally saturated yellow solution. Slow cool at 2 \\u00b0C/h to 0 \\u00b0C, to form small, yellow, sheetlike crystals of the desired (AEQT)PbBr4 compound. To prevent deforming the thin crystals, remove the product from the reaction tube using a pipet and deposit on filter paper to absorb the solution.\",\n        \"experimental_method\": \"Temperature-dependent photoluminescence\",\n        \"experimental_description\": \"Photoluminescence spectra were recorded using a Spex Fluorolog-2 spectrofluorometer. 360 nm light from a xenon arc lamp was used as the excitation source, after being passed through a SPEX 1680 0.22 m double monochromator. The emission was passed through a similar monochromator and detected with a SPEX 1911F photomultiplier tube (PMT).\\r\\nCrystals of the material were pressed between two sapphire windows. The deposit on sapphire was then mounted on a coldfinger. The temperature was maintained using an APD Cryogenics displex system.\",\n        \"physical_property\": \"30.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 851,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbI4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbI4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbI4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbI4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbI4 films at 200 \\u00b0C for 30 min.\",\n        \"experimental_method\": \"Spectrofluorometer\",\n        \"experimental_description\": \"Photoluminescence (PL) spectra was recorded at room temperature on a Spex Fluorolog-2 spectrofluorometer using the front-face geometry. Light from a xenon arc lamp was used as the excitation source, after being passed through a SPEX 1680 0.22 m double monochromator. The wavelength was 370 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 852,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbI4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbI4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbI4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbI4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbI4 films at 200 \\u00b0C for 30 min.\",\n        \"experimental_method\": \"Spectrofluorometer\",\n        \"experimental_description\": \"Photoluminescence excitation (PLE) spectra was recorded at room temperature on a Spex Fluorolog-2 spectrofluorometer using the front-face geometry. Light from a xenon arc lamp was used as the excitation source, after being passed through a SPEX 1680 0.22 m double monochromator. The wavelength was 540 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 853,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbCl4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbCl4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbCl4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbCl4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbCl4 films at 150 \\u00b0C for 5 min.\",\n        \"experimental_method\": \"Spectrofluorometer\",\n        \"experimental_description\": \"Photoluminescence (PL) spectra was recorded at room temperature on a Spex Fluorolog-2 spectrofluorometer using the front-face geometry. Light from a xenon arc lamp was used as the excitation source, after being passed through a SPEX 1680 0.22 m double monochromator. The wavelength was 370 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 854,\n        \"id\": 21,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead chloride\",\n        \"formula\": \"C20H22N2S4PbCl4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetrachloroplumbate(II), AE4TPbCl4, (AEQT)PbCl4, AEQTPbCl4, C20H22S4N2PbCl4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbCl4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbCl4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbCl4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbCl4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbCl4 films at 150 \\u00b0C for 5 min.\",\n        \"experimental_method\": \"Spectrofluorometer\",\n        \"experimental_description\": \"Photoluminescence excitation (PLE) spectra was recorded at room temperature on a Spex Fluorolog-2 spectrofluorometer using the front-face geometry. Light from a xenon arc lamp was used as the excitation source, after being passed through a SPEX 1680 0.22 m double monochromator. The wavelength was 540 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01629\",\n        \"dataset_ID\": 855,\n        \"id\": 231,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"C2H12N2BiBr6Tl\",\n        \"group\": \"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"TlBiBr6, Bismuth bromide thallium\",\n        \"iupac\": \"bis(methanaminium) bismuth thallium bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect-Induced Band-Edge Reconstruction of a Bismuth-Halide Double Perovskite for Visible-Light Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5018\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide ((MA)Br)\",\n        \"synthesis_product\": \"red octahedral single crystals\",\n        \"synthesis_description\": \"TlBr was prepared in lab by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. This resulted in clear, colorless solutions. Next, the (TBA)Br solution was added to the Tl(PF6) solution dropwise and under constant stirring. TlBr resulted as a yellow, solid precipitate and was filtered, washed with MeCN, and added to 1 mL of concentrated HBr, which contained BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The solution was sonicated for 5 minutes, resulting in an orange-red solid that transformed into a deep red. After one hour, the solid was isolated via filtration, residual solvent was removed, and 298 mg of solid yielded. The crystals sat, undisturbed, for 1 week at room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Crystals were coated with Paratone-N oil, placed on a Kapton loop, and moved to a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector. Frames were collected with Mo-k\\u03b1 radiation. Frames were corrected for Lorentz and polarization effects using SAINT 8.27b and absorption effects using SADABS V2012. Structure was solved by direct methods and via SHELXL-2013 software.\",\n        \"physical_property\": \"296.15\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"F m -3 m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01629\",\n        \"dataset_ID\": 861,\n        \"id\": 231,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"C2H12N2BiBr6Tl\",\n        \"group\": \"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"TlBiBr6, Bismuth bromide thallium\",\n        \"iupac\": \"bis(methanaminium) bismuth thallium bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect-Induced Band-Edge Reconstruction of a Bismuth-Halide Double Perovskite for Visible-Light Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5018\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01629\",\n        \"dataset_ID\": 862,\n        \"id\": 231,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"C2H12N2BiBr6Tl\",\n        \"group\": \"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"TlBiBr6, Bismuth bromide thallium\",\n        \"iupac\": \"bis(methanaminium) bismuth thallium bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect-Induced Band-Edge Reconstruction of a Bismuth-Halide Double Perovskite for Visible-Light Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5018\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide (MA)Br\",\n        \"synthesis_product\": \"red octahedral single crystals\",\n        \"synthesis_description\": \"TlBr was prepared in lab by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. This resulted in clear, colorless solutions. Next, the (TBA)Br solution was added to the Tl(PF6) solution dropwise and under constant stirring. TlBr resulted as a yellow, solid precipitate and was filtered, washed with MeCN, and added to 1 mL of concentrated HBr, which contained BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The solution was sonicated for 5 minutes, resulting in an orange-red solid that transformed into a deep red. After one hour, the solid was isolated via filtration, residual solvent was removed, and 298 mg of solid yielded. The crystals sat, undisturbed, for 1 week at room temperature. The polycrystalline powder was coated on a glass slide with grease, mounted in the integrating sphere, and measured with a Cary 6000i spectrometer in reflectance mode.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Solid-state reflectance spectra were collected via a Cary 6000i spectrometer and converted to pseudo-absorbance spectra using the Kubelka-Munk transformation. Band gaps were extracted by fitting linear regions of the Tauc plot (indirect formalism).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01629\",\n        \"dataset_ID\": 863,\n        \"id\": 231,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"C2H12N2BiBr6Tl\",\n        \"group\": \"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"TlBiBr6, Bismuth bromide thallium\",\n        \"iupac\": \"bis(methanaminium) bismuth thallium bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect-Induced Band-Edge Reconstruction of a Bismuth-Halide Double Perovskite for Visible-Light Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5018\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01629\",\n        \"dataset_ID\": 864,\n        \"id\": 231,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"C2H12N2BiBr6Tl\",\n        \"group\": \"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"TlBiBr6, Bismuth bromide thallium\",\n        \"iupac\": \"bis(methanaminium) bismuth thallium bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06+SOC\",\n        \"k_point_grid\": \"6x6x6 \\u0393-centered k-point meshes\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect-Induced Band-Edge Reconstruction of a Bismuth-Halide Double Perovskite for Visible-Light Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5018\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01629\",\n        \"dataset_ID\": 865,\n        \"id\": 231,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"C2H12N2BiBr6Tl\",\n        \"group\": \"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"TlBiBr6, Bismuth bromide thallium\",\n        \"iupac\": \"bis(methanaminium) bismuth thallium bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"X-Ray Absorption Near Edge Structure (XANES)\",\n        \"primary_unit\": \"keV\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"keV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect-Induced Band-Edge Reconstruction of a Bismuth-Halide Double Perovskite for Visible-Light Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5018\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide (MA)Br\",\n        \"synthesis_product\": \"red octahedral single crystals\",\n        \"synthesis_description\": \"TlBr was first synthesized by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. Then, the (TBA)Br solution was added dropwise to the Tl(PF6) solution while being stirred, and TlBr precipitated. This precipitate was added to 1 mL of concentrated HBr with BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The mixture was soniated for 5 minutes and remained undisturbed for one hour to result in single crystals.\",\n        \"experimental_method\": \"X-ray absorption spectroscopy (XAS)\",\n        \"experimental_description\": \"Data were obtained at the Stanford Synchrotron Radiation Lightsource (SSRL) with beamline 2-2 at room temperature. A Lytle fluorescence detector was used in transmission mode to measure the XAS data, using a selenium foil for reference. The inflection point on the selenium rising edge was fixed at 12658 eV, and the spectra were normalized.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b01629\",\n        \"dataset_ID\": 867,\n        \"id\": 231,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"C2H12N2BiBr6Tl\",\n        \"group\": \"(MA)2BiBr6Tl, (CH3NH3)2BiBr6Tl, bis(methanaminium) tribromobismuthate(III) tribromothalliate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"TlBiBr6, Bismuth bromide thallium\",\n        \"iupac\": \"bis(methanaminium) bismuth thallium bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Raman Shift\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Raman Shift\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect-Induced Band-Edge Reconstruction of a Bismuth-Halide Double Perovskite for Visible-Light Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5018\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Tl(PF6), (TBA)Br (TBA = tetrabutylammonium), MeCN, HBr, BiBr3, methylammonium bromide (MA)Br\",\n        \"synthesis_product\": \"red octahedral single crystals\",\n        \"synthesis_description\": \"TlBr was first synthesized by dissolving solid Tl(PF6) (160 mg, 0.458 mmol) and (TBA)Br (221 mg, 0.686 mmol) separately in 3 mL of MeCN. Then, the (TBA)Br solution was added dropwise to the Tl(PF6) solution while being stirred, and TlBr precipitated. This precipitate was added to 1 mL of concentrated HBr with BiBr3 (411 mg, 0.915 mmol) and (MA)Br (205 mg, 1.83 mmol). The mixture was soniated for 5 minutes and remained undisturbed for one hour to result in single crystals.\",\n        \"experimental_method\": \"Raman microscopy\",\n        \"experimental_description\": \"The spectrum was recorded using a Renishaw RM1000 Raman microscope\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 869,\n        \"id\": 2,\n        \"compound_name\": \"Bis(phenylethylammonium) lead chloride\",\n        \"formula\": \"C16H24N2PbCl4\",\n        \"group\": \"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PEA)2PbCl4, (C8H12N)2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 870,\n        \"id\": 13,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead chloride\",\n        \"formula\": \"C14H20N2PbCl4\",\n        \"group\": \"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 871,\n        \"id\": 14,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead chloride\",\n        \"formula\": \"C22H24N2PbCl4\",\n        \"group\": \"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NMA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 872,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 873,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 874,\n        \"id\": 10,\n        \"compound_name\": \"Bis(2-(2-naphtyl)ethanammonium) lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) tetrabromoplumbate(II), NEA2PbBr4, (C12H14N)2PbBr4, (C12H11NH3)2PbBr4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-(napthalen-2-yl)ethane-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NEA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 875,\n        \"id\": 7,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead bromide\",\n        \"formula\": \"C22H24N2PbBr4\",\n        \"group\": \"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"NMA2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NMA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin-film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 877,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Visible absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 878,\n        \"id\": 12,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Visible absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 879,\n        \"id\": 6,\n        \"compound_name\": \"Bis(2-(2-naphthyl)ethanammonium) lead iodide\",\n        \"formula\": \"C24H28N2PbI4\",\n        \"group\": \"2-(2-naphthyl)ethane-1-aminium tetraiodoplumbate(II), NEA2PbI4, (C24H28N2)PbI4\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-(2-naphthyl)ethane-1-aminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"NEA2PbI4, (C24H28N2)PbI4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(NEA)2PbI4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin-film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pn\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5sc01135c\",\n        \"dataset_ID\": 881,\n        \"id\": 232,\n        \"compound_name\": \"Bis(3,4-dichlorobut-3-en-1-ammonium) lead bromide\",\n        \"formula\": \"C8H20Cl4N2PbBr4\",\n        \"group\": \"(BEA-Cl2)2[PbBr4], C8H20Br4Cl4N2Pb, bis(3,4-dichlorobut-3-en-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H10Cl2N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(3,4-dichlorobut-3-en-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Post-synthetic Halide Conversion and Selective Halogen Capture in Hybrid Perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"6\",\n        \"pages_start\": \"4054\",\n        \"pages_end\": \"4059\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5sc01135c\",\n        \"dataset_ID\": 882,\n        \"id\": 233,\n        \"compound_name\": \"Bis(3,4-dibromobut-3-en-1-ammonium) lead bromide\",\n        \"formula\": \"C8H20Br4N2PbBr4\",\n        \"group\": \"(BEA-Br2)2[PbBr4], C8H20Br8N2Pb, bis(3,4-dibromobut-3-en-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H10Br2N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(3,4-dibromobut-3-en-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Post-synthetic Halide Conversion and Selective Halogen Capture in Hybrid Perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"6\",\n        \"pages_start\": \"4054\",\n        \"pages_end\": \"4059\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5sc01135c\",\n        \"dataset_ID\": 883,\n        \"id\": 234,\n        \"compound_name\": \"Bis(3,4-dibromobut-3-en-1-ammonium) lead chloride\",\n        \"formula\": \"C8H20Br4N2PbCl4\",\n        \"group\": \"(BEA-Br2)2[PbCl4], C8H20Br4N2PbCl4, bis(3,4-dibromobut-3-en-1-aminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C4H10Br2N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(3,4-dibromobut-3-en-1-aminium) lead (II) chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Post-synthetic Halide Conversion and Selective Halogen Capture in Hybrid Perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"6\",\n        \"pages_start\": \"4054\",\n        \"pages_end\": \"4059\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"200.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5sc01135c\",\n        \"dataset_ID\": 884,\n        \"id\": 233,\n        \"compound_name\": \"Bis(3,4-dibromobut-3-en-1-ammonium) lead bromide\",\n        \"formula\": \"C8H20Br4N2PbBr4\",\n        \"group\": \"(BEA-Br2)2[PbBr4], C8H20Br8N2Pb, bis(3,4-dibromobut-3-en-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H10Br2N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(3,4-dibromobut-3-en-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Post-synthetic Halide Conversion and Selective Halogen Capture in Hybrid Perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"6\",\n        \"pages_start\": \"4054\",\n        \"pages_end\": \"4059\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"(BEA)Cl (but-3-en-1-ammonium chloride), methanol, Cl\\u00ac2 (g), PbBr2, 9-M HBr\",\n        \"synthesis_product\": \"Colorless plate-like crystals\",\n        \"synthesis_description\": \"First, a solution of (BEA)Cl (0.10 g, 0.93 mmol) in 10 mL of methanol was cooled to 0 \\u00ba C, exposed to Cl2 gas for 2 minutes, and then allowed to stir for 1 hour in the dark. During this time, volatiles were removed under reduced pressure, and a colorless solid resulted. This solid was then dissolved in 3 mL of methanol and added to a stirred, 5-mL solution of PbBr2 (0.17 g, 0.46 mmol) in 9-M HBr at -10 \\u00ac\\u00ba C. After 10 minutes, a colorless precipitate was filtered through a glass frit and washed with diethyl ether at -10 \\u00ba C. A colorless crystalline solid resulted and was held at reduced pressure for 1 hour to produce 0.303 g of product.\",\n        \"experimental_method\": \"Single-crystal X-Ray diffraction\",\n        \"experimental_description\": \"The data were recorded using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo k\\u03b1 radiation. Data was corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5sc01135c\",\n        \"dataset_ID\": 885,\n        \"id\": 232,\n        \"compound_name\": \"Bis(3,4-dichlorobut-3-en-1-ammonium) lead bromide\",\n        \"formula\": \"C8H20Cl4N2PbBr4\",\n        \"group\": \"(BEA-Cl2)2[PbBr4], C8H20Br4Cl4N2Pb, bis(3,4-dichlorobut-3-en-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H10Cl2N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(3,4-dichlorobut-3-en-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Post-synthetic Halide Conversion and Selective Halogen Capture in Hybrid Perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"6\",\n        \"pages_start\": \"4054\",\n        \"pages_end\": \"4059\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"(BEA)Cl (but-3-en-1-ammonium chloride), methanol, Cl\\u00ac2 (g), PbBr2, 9-M HBr\",\n        \"synthesis_product\": \"Colorless plate-like crystals\",\n        \"synthesis_description\": \"First, a solution of (BEA)Cl (0.10 g, 0.93 mmol) in 10 mL of methanol was cooled to 0 \\u00ba C, exposed to Cl2 gas for 2 minutes, and then allowed to stir for 1 hour in the dark. During this time, volatiles were removed under reduced pressure, and a colorless solid resulted. \\r\\nThis solid was then dissolved in 3 mL of methanol and added to a stirred, 5-mL solution of PbBr2 (0.17 g, 0.46 mmol) in 9-M HBr at -10 \\u00ac\\u00ba C. After 10 minutes, a colorless precipitate was filtered through a glass frit and washed with diethyl ether at -10 \\u00ba C. A colorless crystalline solid resulted and was held at reduced pressure for 1 hour to produce 0.303 g of product.\",\n        \"experimental_method\": \"Single-crystal X-Ray diffraction\",\n        \"experimental_description\": \"The data were recorded using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo k\\u03b1 radiation. Data was corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c5sc01135c\",\n        \"dataset_ID\": 886,\n        \"id\": 234,\n        \"compound_name\": \"Bis(3,4-dibromobut-3-en-1-ammonium) lead chloride\",\n        \"formula\": \"C8H20Br4N2PbCl4\",\n        \"group\": \"(BEA-Br2)2[PbCl4], C8H20Br4N2PbCl4, bis(3,4-dibromobut-3-en-1-aminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C4H10Br2N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(3,4-dibromobut-3-en-1-aminium) lead (II) chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Post-synthetic Halide Conversion and Selective Halogen Capture in Hybrid Perovskites\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"6\",\n        \"pages_start\": \"4054\",\n        \"pages_end\": \"4059\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Single-crystal X-Ray diffraction\",\n        \"experimental_description\": \"The data were recorded using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo k\\u03b1 radiation. Data was corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\",\n        \"physical_property\": \"200.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201309786\",\n        \"dataset_ID\": 887,\n        \"id\": 235,\n        \"compound_name\": \"Bis(3-butylidyne-1-ammonium) lead bromide\",\n        \"formula\": \"C8H16N2PbBr4\",\n        \"group\": \"(BYA)2[PbBr4], C8H16Br4N2Pb, bis(3-butylidyne-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H8N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(3-butylidyne-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible and Irreversible Chemisorption in Nonporous-Crystalline Hybrids\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"53\",\n        \"pages_start\": \"1039\",\n        \"pages_end\": \"1042\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201309786\",\n        \"dataset_ID\": 888,\n        \"id\": 236,\n        \"compound_name\": \"Bis(1,2-diiodo-but-1-en-4-ammonium) lead bromide\",\n        \"formula\": \"C8H16I4N2PbBr4\",\n        \"group\": \"(BYA-I2)2[PbBr4], C8H16Br4I4N2Pb, bis(1,2-diiodo-but-1-en-4-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H8I2N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(1,2-diiodo-but-1-en-4-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible and Irreversible Chemisorption in Nonporous-Crystalline Hybrids\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"53\",\n        \"pages_start\": \"1039\",\n        \"pages_end\": \"1042\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201309786\",\n        \"dataset_ID\": 889,\n        \"id\": 237,\n        \"compound_name\": \"Bis(but-3-en-1-ammonium) lead bromide\",\n        \"formula\": \"C8H20N2PbBr4\",\n        \"group\": \"(BEA)2[PbBr4], C8H20Br4N2Pb, bis(but-3-en-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(but-3-en-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible and Irreversible Chemisorption in Nonporous-Crystalline Hybrids\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"53\",\n        \"pages_start\": \"1039\",\n        \"pages_end\": \"1042\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201309786\",\n        \"dataset_ID\": 890,\n        \"id\": 235,\n        \"compound_name\": \"Bis(3-butylidyne-1-ammonium) lead bromide\",\n        \"formula\": \"C8H16N2PbBr4\",\n        \"group\": \"(BYA)2[PbBr4], C8H16Br4N2Pb, bis(3-butylidyne-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H8N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(3-butylidyne-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible and Irreversible Chemisorption in Nonporous-Crystalline Hybrids\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"53\",\n        \"pages_start\": \"1039\",\n        \"pages_end\": \"1042\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"(BYA)Cl (but-3-yn-1-ammonium chloride), methanol, PbBr2, 9-M HBr\",\n        \"synthesis_product\": \"colorless crystals\",\n        \"synthesis_description\": \"First, 3 mL of (BYA)Cl (0.200 g, 1.89 mmol) in methanol was added to a 3-mL solution of PbBr2 (0.340 g, 0.93 mmol) in 9-M HBr at a temperature of -10\\u00baC. The solution was stirred continuously during this process. After 15 minutes, a colorless precipitate formed and was filtered at -10\\u00ba C via a glass frit and washed with cold diethyl ether.  Afterward, the colorless crystalline solid was held at reduced pressure for an hour and therefore produced 0.536 g of product. To obtain crystals appropriate for single-crystal X-ray diffraction, slow evaporation of the concentrated solution in a 1:1 methanol: HBr (9-M) was performed.\",\n        \"experimental_method\": \"Single-crystal X-Ray Diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation. Data were corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201309786\",\n        \"dataset_ID\": 891,\n        \"id\": 236,\n        \"compound_name\": \"Bis(1,2-diiodo-but-1-en-4-ammonium) lead bromide\",\n        \"formula\": \"C8H16I4N2PbBr4\",\n        \"group\": \"(BYA-I2)2[PbBr4], C8H16Br4I4N2Pb, bis(1,2-diiodo-but-1-en-4-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H8I2N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(1,2-diiodo-but-1-en-4-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible and Irreversible Chemisorption in Nonporous-Crystalline Hybrids\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"53\",\n        \"pages_start\": \"1039\",\n        \"pages_end\": \"1042\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"(BYA)Cl (but-3-yn-1-ammonium chloride), methanol, PbBr2, 9-M HBr, I2 crystals\",\n        \"synthesis_product\": \"colorless crystals\",\n        \"synthesis_description\": \"First, 3 mL of (BYA)Cl (0.200 g, 1.89 mmol) in methanol was added to a 3-mL solution of PbBr2 (0.340 g, 0.93 mmol) in 9-M HBr at a temperature of -10\\u00baC. The solution was stirred continuously during this process. After 15 minutes, a colorless precipitate formed and was filtered at -10\\u00ba C via a glass frit and washed with cold diethyl ether. Afterward, the colorless crystalline solid was held at reduced pressure for an hour and therefore produced 0.536 g of product. 0.1 mmol of the obtained crystals were kept in a sealed darkened glass jar with 1.5 \\u2013 2.0 g of iodine crystals. The crystals were kept at reduced pressure for 30 mins to remove the surface-adsorbed iodine.\",\n        \"experimental_method\": \"Single-crystal X-Ray Diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation. Data were corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201309786\",\n        \"dataset_ID\": 892,\n        \"id\": 237,\n        \"compound_name\": \"Bis(but-3-en-1-ammonium) lead bromide\",\n        \"formula\": \"C8H20N2PbBr4\",\n        \"group\": \"(BEA)2[PbBr4], C8H20Br4N2Pb, bis(but-3-en-1-aminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(but-3-en-1-aminium) lead (II) bromide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible and Irreversible Chemisorption in Nonporous-Crystalline Hybrids\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"53\",\n        \"pages_start\": \"1039\",\n        \"pages_end\": \"1042\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"(BEA)Cl (but-3-en-1-ammonium chloride), methanol, PbBr2, 9-M HBr\",\n        \"synthesis_product\": \"colorless crystals\",\n        \"synthesis_description\": \"First, 3 mL of (BEA)Cl (0.200 g, 1.86 mmol) in methanol was added to a 3-mL solution of PbBr2 (0.330 g, 0.90 mmol) in 9-M HBr at a temperature of -10\\u00baC. The solution was stirred continuously during this process. After 15 minutes, a colorless precipitate formed and was filtered via a glass frit and washed with diethyl ether. This process was also executed at -10\\u00ba C. Afterward, a colorless crystalline solid was held at reduced pressure for an hour and therefore produced 0.425 g of product. To obtain crystals appropriate for single-crystal X-ray diffraction, acetone was slowly diffused into a concentrated solution of the product in 9-M HBr.\",\n        \"experimental_method\": \"Single-crystal X-Ray Diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker D8 Venture diffractometer with a Photon 100 CMOS detector and Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation. Data were corrected via the SAINT 8.27b and SADABS V2012 packages. Structures were solved via direct methods and via SHELXS-97.\",\n        \"physical_property\": \"296.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201505055\",\n        \"dataset_ID\": 893,\n        \"id\": 238,\n        \"compound_name\": \"tris(methylammonium) bismuth iodide\",\n        \"formula\": \"C3H18N3Bi2I9\",\n        \"group\": \"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"tris(methanaminium) bismuth iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA-PBE + SO\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Methylammonium Bismuth Iodide as a Lead-Free, Stable Hybrid Organic\\u2013Inorganic Solar Absorber\",\n        \"journal\": \"Chemistry: A European Journal\",\n        \"vol\": \"22\",\n        \"pages_start\": \"2605\",\n        \"pages_end\": \"2610\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Solution-assisted MBI was placed on borosilicate glass and quartz substrates, which were cleaned ultrasonically and with oxygen plasma. A solution of BiI3 was prepared by dissolving BiI3 (200 mg) in 0.5 mL DMF. This solution was mixed for one hour before being filtered through a 0.2 \\u03bcm PTFEsyringe filter. Next, 10\\u03bcL of the filtered solution was spread on a substrate, spin-cast (3000 rpm for 5s, 6000 rpm for 5s). BiI\\u00ac3 film was dried for 30 minutes and annealed at 100\\u00baC for half an hour. In the meantime, methylammonium iodide was dissolved in anhydrous isopropanol (6 mg mL-1). 200 \\u03bcL of methylammonium iodide was then deposited on the BiI3 film for one minute before spinning and finally being annealed at 100\\u00baC for 1 hour.\",\n        \"experimental_method\": \"PXRD\",\n        \"experimental_description\": \"Rietveld refinement. Powder X-Ray diffraction was performed with a PANanalytical X\\u2019Pert PRO XRPD using Cu K\\u03b1 radiation (1.5406 \\u00c5). PXRD of MBI was performed by grazing incident X-ray diffraction (GIXD) using Rigaku SmartLab using Cu K\\u03b1 radiation (1.5406 \\u00c5 wavelength) and incident angle 0.5\\u00ba.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201505055\",\n        \"dataset_ID\": 895,\n        \"id\": 238,\n        \"compound_name\": \"tris(methylammonium) bismuth iodide\",\n        \"formula\": \"C3H18N3Bi2I9\",\n        \"group\": \"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"tris(methanaminium) bismuth iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Methylammonium Bismuth Iodide as a Lead-Free, Stable Hybrid Organic\\u2013Inorganic Solar Absorber\",\n        \"journal\": \"Chemistry: A European Journal\",\n        \"vol\": \"22\",\n        \"pages_start\": \"2605\",\n        \"pages_end\": \"2610\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"BiI3 (99.999%, Alfa Aesar), N, N-Dimethylformamide (DMF, Sigma-Aldrich), Methylammonium iodide (MAI, Luminescence Technology Corp.),\",\n        \"synthesis_product\": \"film on quartz substrates\",\n        \"synthesis_description\": \"200 mg BiI3 powder was dissolved in 0.5 mL DMF. 20 \\u03bcL of this solution was heated at 150 \\u00b0C on a hotplate for 30 s. The solution was then spin-coated at 4000 rpm for 10 s. The film was annealed at 100 \\u00b0C. The film was kept over MAI powder heated at 150 \\u00b0C for 4 hr under vacuum. The film was then cooled to room temperature and was washed with anhydrous isopropanol. Finally, it was annealed for 1 hr at 100 \\u00b0C in a nitrogen-filled glovebox.\",\n        \"experimental_method\": \"Photoluminescence with integrating sphere\",\n        \"experimental_description\": \"PL quantum efficiency measurements were performed using an integrating sphere (Labsphere RTC-060-\\r\\nSF). A 405 nm wavelength diode laser as excitation source, and a 535 nm longpass Schott glass filter.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201505055\",\n        \"dataset_ID\": 896,\n        \"id\": 238,\n        \"compound_name\": \"tris(methylammonium) bismuth iodide\",\n        \"formula\": \"C3H18N3Bi2I9\",\n        \"group\": \"MBI, MA3Bi2I9, (CH3NH3)3Bi2I9, tris(methanaminium) nonaiodo dibismuthate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"tris(methanaminium) bismuth iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Methylammonium Bismuth Iodide as a Lead-Free, Stable Hybrid Organic\\u2013Inorganic Solar Absorber\",\n        \"journal\": \"Chemistry: A European Journal\",\n        \"vol\": \"22\",\n        \"pages_start\": \"2605\",\n        \"pages_end\": \"2610\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"BiI3 (99.999%, Alfa Aesar), N, N-Dimethylformamide (DMF, Sigma-Aldrich), Methylammonium iodide (MAI, Luminescence Technology Corp.)\",\n        \"synthesis_product\": \"film on quartz substrates\",\n        \"synthesis_description\": \"200 mg BiI3 powder was dissolved in 0.5 mL DMF. The solution was filtered through a 0.2 \\u03bcm PTFE syringe filter. 10 \\u03bcL of the solution was spin-coated at 3000 rpm for 5 s, followed by 6000 rpm for 5 s. The film was dried for 30 min and was annealed at 100 \\u00b0C for 30 min. an MAI solution of concentration of 6 mg\\u00b7mL-1in anhydrous isopropanol was prepared.  200 \\u03bcL of MAI solution was kept on the BiI3 film for 60 s. The film was then spun at 4000 rpm for 20 s. The film was finally annealed at 100 \\u00b0C for 1 hr.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Photoluminescence spectra were acquired using a FluoroMax-3, excitation wavelength of 360 nm, and slit size of 5 nm\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.7b02322\",\n        \"dataset_ID\": 902,\n        \"id\": 241,\n        \"compound_name\": \"bis(methylammonium) potassium gadolinium chloride\",\n        \"formula\": \"C2H12N2KGdCl6\",\n        \"group\": \"(MA)2KGdCl6, (CH3NH3)2KGdCl6, bis(methanaminium) trichlorogadoliniate(III) tripotassiate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"KGdCl6, Potassium chloride gadolinium\",\n        \"iupac\": \"bis(methanaminium) potassium gadolinium chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"optB86b-vdW\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Characterization of the Rare-Earth Hybrid Double Perovskites: (CH3NH3)2KGdCl6 and (CH3NH3)2KYCl6\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5020\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.7b02322\",\n        \"dataset_ID\": 903,\n        \"id\": 242,\n        \"compound_name\": \"bis(methylammonium) potassium yttrium chloride\",\n        \"formula\": \"C2H12N2KYCl6\",\n        \"group\": \"(MA)2KYCl6, (CH3NH3)2KYCl6, bis(methanaminium) trichloropotassiate(I) trichloroyttriate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"KYCl6, Potassium chloride yttrium\",\n        \"iupac\": \"bis(methanaminium) potassium yttrium chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP Package\",\n        \"level_of_theory\": \"DFT (van der Waals-corrected)\",\n        \"xc_functional\": \"Van der Waals density functional method (optB86b-vdW); specifically, PBE, (PBE+D2 and PBE+D3), (PBE+TS), PBEsol.\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Characterization of the Rare-Earth Hybrid Double Perovskites: (CH3NH3)2KGdCl6 and (CH3NH3)2KYCl6\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5020\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Y2O3, KCl, (MA)Cl, HCl\",\n        \"synthesis_product\": \"clear, colorless crystals\",\n        \"synthesis_description\": \"Y2O3 (1 mmol), KCl (1 mmol), and (MA)Cl (2 mmol) were dissolved in 2 mL of HCl solution (32 wt %). The solution was placed in a covered, glass vial on a hot place at 80\\u00ba, stirred for one hour at this temperature (until the solution became clear), and the cap was finally opened. The solution evaporated until dry at 85\\u00ba. Crystals were selected from the dry sample.\",\n        \"experimental_method\": \"Variable Temperature Single Crystal X-ray Diffraction (VT-SCXRD)\",\n        \"experimental_description\": \"Crystals were selected for further analysis, placed on an Xcalibur/Gemini Ultra diffractometer with an Eos CCD area detector via Paratone-N. Structures were solved via direct methods via Olex 2 and ShelXS structure solution program. They were further refined with ShelXL refinement package.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.7b02322\",\n        \"dataset_ID\": 904,\n        \"id\": 242,\n        \"compound_name\": \"bis(methylammonium) potassium yttrium chloride\",\n        \"formula\": \"C2H12N2KYCl6\",\n        \"group\": \"(MA)2KYCl6, (CH3NH3)2KYCl6, bis(methanaminium) trichloropotassiate(I) trichloroyttriate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"KYCl6, Potassium chloride yttrium\",\n        \"iupac\": \"bis(methanaminium) potassium yttrium chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"optB86b-vdW\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Characterization of the Rare-Earth Hybrid Double Perovskites: (CH3NH3)2KGdCl6 and (CH3NH3)2KYCl6\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5020\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 905,\n        \"id\": 243,\n        \"compound_name\": \"Cesium silver thallium chloride\",\n        \"formula\": \"Cs2AgTlCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichlorothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Solid CsCl, AgCl, Tl2O3, HCl, H2O\",\n        \"synthesis_product\": \"dark red, truncated octahedral crystals\",\n        \"synthesis_description\": \"First, solid CsCl (101 mg, 0.600 mmol), AgCl (21 mg, 0.15 mmol), and Tl2O3 (34 mg, 0.075 mmol) were mixed in a 20 mL glass with 8 mL of H2O and 8 mL of HCl (12M). This resulted in a colorless, 6M HCl solution. The vial was sealed with a polystyrene cap, heated to 100\\u00baC for 4-6 hours until AgCl dissolved completely, and then the vial was cooled to room temperature.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were recorded using a Bruker D8 Venture diffractometer (with Photon 100 CMOS detector) with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5). Data frames were then corrected for Lorentz/polarization using SAINT V8.38A and absorption effects using SADABS V2012.\",\n        \"physical_property\": \"296.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 906,\n        \"id\": 243,\n        \"compound_name\": \"Cesium silver thallium chloride\",\n        \"formula\": \"Cs2AgTlCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichlorothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Solid CsCl, AgCl, Tl2O3, HCl, H2O\",\n        \"synthesis_product\": \"dark red, truncated octahedral crystals\",\n        \"synthesis_description\": \"First, solid CsCl (101 mg, 0.600 mmol), AgCl (21 mg, 0.15 mmol), and Tl2O3 (34 mg, 0.075 mmol) were mixed in a 20 mL glass with 8 mL of H2O and 8 mL of HCl (12M). This resulted in a colorless, 6M HCl solution. The vial was sealed with a polystyrene cap, heated to 100\\u00baC for 4-6 hours until AgCl dissolved completely, and then the vial was cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance (reflectance mode)\",\n        \"experimental_description\": \"The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 907,\n        \"id\": 243,\n        \"compound_name\": \"Cesium silver thallium chloride\",\n        \"formula\": \"Cs2AgTlCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichlorothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT + one-shot GW\",\n        \"xc_functional\": \"G0W0@HSE06\",\n        \"k_point_grid\": \"2x2x2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 910,\n        \"id\": 244,\n        \"compound_name\": \"Cesium silver thallium bromide\",\n        \"formula\": \"Cs2AgTlBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Solid CsBr, AgBr, Tl2O3, HBr\",\n        \"synthesis_product\": \"Black, truncated octahedral crystals\",\n        \"synthesis_description\": \"First, solid CsBr(533 mg, 2.50 mmol), AgBr (940 mg, 5.01 mmol), and Tl2O3 (285 mg, 0.625 mmol) were mixed with 20 mL of HBr (8.9M). The vial was sealed with a polystyrene cap, heated to 100\\u00baC for 2 hours until solids dissolved, resulting in a pale, yellow solution. Then, the vial was cooled to room temperature.\",\n        \"experimental_method\": \"single crystal X-ray diffraction (XRD)\",\n        \"experimental_description\": \"The frames were recorded using a Bruker D8 Venture diffractometer (with Photon 100 CMOS detector) with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5). Data frames were then corrected for Lorentz/polarization using SAINT V8.38A and absorption effects using SADABS V2012.\",\n        \"physical_property\": \"296.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 911,\n        \"id\": 243,\n        \"compound_name\": \"Cesium silver thallium chloride\",\n        \"formula\": \"Cs2AgTlCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichlorothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Solid CsCl, AgCl, Tl2O3, HCl, H2O\",\n        \"synthesis_product\": \"dark red, truncated octahedral crystals\",\n        \"synthesis_description\": \"First, solid CsCl (101 mg, 0.600 mmol), AgCl (21 mg, 0.15 mmol), and Tl2O3 (34 mg, 0.075 mmol) were mixed in a 20 mL glass with 8 mL of H2O and 8 mL of HCl (12M). This resulted in a colorless, 6M HCl solution. The vial was sealed with a polystyrene cap, heated to 100\\u00baC for 4-6 hours until AgCl dissolved completely, and then the vial was cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance (reflectance mode)\",\n        \"experimental_description\": \"The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 912,\n        \"id\": 244,\n        \"compound_name\": \"Cesium silver thallium bromide\",\n        \"formula\": \"Cs2AgTlBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Solid CsBr, AgBr, Tl2O3, HBr\",\n        \"synthesis_product\": \"Black, truncated octahedral crystals\",\n        \"synthesis_description\": \"First, solid CsBr(533 mg, 2.50 mmol), AgBr (940 mg, 5.01 mmol), and Tl2O3 (285 mg, 0.625 mmol) were mixed with 20 mL of HBr (8.9M). The vial was sealed with a polystyrene cap, heated to 100\\u00baC for 2 hours until solids dissolved, resulting in a pale, yellow solution. Then, the vial was cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance (reflectance mode)\",\n        \"experimental_description\": \"The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 913,\n        \"id\": 244,\n        \"compound_name\": \"Cesium silver thallium bromide\",\n        \"formula\": \"Cs2AgTlBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Solid CsBr, AgBr, Tl2O3, HBr\",\n        \"synthesis_product\": \"Black, truncated octahedral crystals\",\n        \"synthesis_description\": \"First, solid CsBr(533 mg, 2.50 mmol), AgBr (940 mg, 5.01 mmol), and Tl2O3 (285 mg, 0.625 mmol) were mixed with 20 mL of HBr (8.9M). The vial was sealed with a polystyrene cap, heated to 100\\u00baC for 2 hours until solids dissolved, resulting in a pale, yellow solution. Then, the vial was cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance (reflectance mode)\",\n        \"experimental_description\": \"The reflectance spectrum was recorded using a Cary 6000i spectrometer. Kubelka-Munk transformation was used to obtain the absorption spectrum. Tauc plot with direct band gap assumption was used for obtaining the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201807421\",\n        \"dataset_ID\": 914,\n        \"id\": 244,\n        \"compound_name\": \"Cesium silver thallium bromide\",\n        \"formula\": \"Cs2AgTlBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromothalliate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgTlBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-06-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT + one-shot GW\",\n        \"xc_functional\": \"G0W0@HSE06\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small-Band-Gap Halide Double Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"12765\",\n        \"pages_end\": \"12770\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 915,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Conductivity\",\n        \"primary_unit\": \"S\\u2022cm^{-1}\",\n        \"secondary_name\": \"pressure\",\n        \"secondary_unit\": \"GPa\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"pellet\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",\n        \"synthesis_product\": \"yellow-green powder\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at a reduced temperature for 12 hours.\",\n        \"experimental_method\": \"Cross-type DAC.\",\n        \"experimental_description\": \"Solid sample was placed in insulating boron nitride gasket, which connected to 4 platinum leads. The leads lead into a sample cavity. Adjacent leads were coupled, the gasket was mounted into a cross-type DAC, and platinum leads were connected to external leads. The DAC was cooled to lower temperatures and raised to higher temperatures (between 274 and 310 K); each temperature was measured when the diamond was a consistent temperature. Current-voltage curves were generated from -40 to 40 mV at a scan rate of 1 mVs^{-1}, and conductivity was calculated by using slope of averaged curves, sample thickness, and distance between leads.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 916,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"pellet\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",\n        \"synthesis_product\": \"yellow-green powder\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at a reduced temperature for 12 hours.\",\n        \"experimental_method\": \"resistivity measurements\",\n        \"experimental_description\": \"Four platinum lead resistivity set-up was used in a diamond anvil cell (DAC).\",\n        \"physical_property\": \"51.4\",\n        \"unit\": \"GPa\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja512396m\",\n        \"dataset_ID\": 917,\n        \"id\": 222,\n        \"compound_name\": \"(2,2'-(ethylenedioxy)bis(ethylammonium) copper chloride\",\n        \"formula\": \"C6H18O2N2CuCl4\",\n        \"group\": \"(EDBE)[CuCl4], ((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) tetrachlorostannate(II) \",\n        \"organic\": \"C6H18O2N2\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"((ethane-1,2-dyilbis(oxy))-O,O'-bis(ethanaminium) copper chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"pellet\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Pressure-Induced Conductivity and Yellow-to-Black Piezochromism in a Layered Cu\\u2212Cl Hybrid Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"1673\",\n        \"pages_end\": \"1678\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"2,2\\u2019-(ethylenedioxy)bis(ethylamine), CuCl2, 12-M HCl\",\n        \"synthesis_product\": \"yellow-green powder\",\n        \"synthesis_description\": \"First, a 20mL solution of 2,2\\u2019-(ethylenedioxy)bis(ethylamine) (1.10 g, 7.40 mmol) in ethanol was added to a 20mL solution of CuCl2 (1.00 g, 7.44 mmol) in ethanol, and a solution fo 12-M HCl (1.75 mL, 21.0 mmol) was added to the mixture soon thereafter. A yellow-green precipitate formed within 10 minutes and was drained and washed with diethyl ether (5x5 mL). 2.30 g of product was obtained by keeping the yellow-green powder at a reduced temperature for 12 hours.\",\n        \"experimental_method\": \"resistivity measurements\",\n        \"experimental_description\": \"Four platinum lead resistivity set-up was used in a diamond anvil cell (DAC).\",\n        \"physical_property\": \"40.2\",\n        \"unit\": \"GPa\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 918,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            919,\n            937\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GW0\",\n        \"k_point_grid\": \"4x4x4\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 919,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            918,\n            937\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"BSE\",\n        \"k_point_grid\": \"16x16x16\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 920,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            921,\n            936\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GW0\",\n        \"k_point_grid\": \"4x3x1\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 921,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            920,\n            936\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"BSE\",\n        \"k_point_grid\": \"16x12x4\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 924,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"CP2K\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-SIC\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"Gaussian+PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 926,\n        \"id\": 102,\n        \"compound_name\": \"N, N\\u2032-dimethylethylenediamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N, N\\u201a\\u00c4\\u2264-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N, N\\u2032-dimethylethylenediaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            927,\n            928\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GW0\",\n        \"k_point_grid\": \"2x4x2\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 927,\n        \"id\": 102,\n        \"compound_name\": \"N, N\\u2032-dimethylethylenediamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N, N\\u201a\\u00c4\\u2264-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N, N\\u2032-dimethylethylenediaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            926,\n            928\n        ],\n        \"primary_name\": \"band gap (optical, theory)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GW0\",\n        \"k_point_grid\": \"2x4x2\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 928,\n        \"id\": 102,\n        \"compound_name\": \"N, N\\u2032-dimethylethylenediamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N, N\\u201a\\u00c4\\u2264-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N, N\\u2032-dimethylethylenediaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            926,\n            927\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GW0\",\n        \"k_point_grid\": \"2x4x2\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 929,\n        \"id\": 102,\n        \"compound_name\": \"N, N\\u2032-dimethylethylenediamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N, N\\u201a\\u00c4\\u2264-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N, N\\u2032-dimethylethylenediaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CP2K\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE-SIC\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"Gaussian+PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 930,\n        \"id\": 117,\n        \"compound_name\": \"Cesium tin bromide (0D)\",\n        \"formula\": \"Cs4SnBr6\",\n        \"group\": \"tetracesium hexabromostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            931,\n            932\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CP2K\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE0\",\n        \"k_point_grid\": \"2x2x2\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"Gaussian+PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 931,\n        \"id\": 117,\n        \"compound_name\": \"Cesium tin bromide (0D)\",\n        \"formula\": \"Cs4SnBr6\",\n        \"group\": \"tetracesium hexabromostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            930,\n            932\n        ],\n        \"primary_name\": \"band gap (optical, theory)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CP2K\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE0\",\n        \"k_point_grid\": \"2x2x2\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"Gaussian+PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 932,\n        \"id\": 117,\n        \"compound_name\": \"Cesium tin bromide (0D)\",\n        \"formula\": \"Cs4SnBr6\",\n        \"group\": \"tetracesium hexabromostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            930,\n            931\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CP2K\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE0\",\n        \"k_point_grid\": \"2x2x2\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"Gaussian+PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 934,\n        \"id\": 117,\n        \"compound_name\": \"Cesium tin bromide (0D)\",\n        \"formula\": \"Cs4SnBr6\",\n        \"group\": \"tetracesium hexabromostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CP2K\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE0\",\n        \"k_point_grid\": \"2x2x2\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"Gaussian+PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 936,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            920,\n            921\n        ],\n        \"primary_name\": \"band gap (optical, theory)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GW0\",\n        \"k_point_grid\": \"4x3x1\",\n        \"level_of_relativity\": \"SOC\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.8b03717\",\n        \"dataset_ID\": 937,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            918,\n            919\n        ],\n        \"primary_name\": \"band gap (optical, theory)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GW0\",\n        \"k_point_grid\": \"4x4x4\",\n        \"level_of_relativity\": \"scalar\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Atomistic Mechanism of Broadband Emission in Metal Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"501\",\n        \"pages_end\": \"506\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06276\",\n        \"dataset_ID\": 940,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP 5.4.4\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"4x2x2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Stable Lead-Free Perovskite Field-Effect Transistors Incorporating Linear \\u03c0\\u2010Conjugated Organic Ligands\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15577\",\n        \"pages_end\": \"15585\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06276\",\n        \"dataset_ID\": 941,\n        \"id\": 245,\n        \"compound_name\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"formula\": \"C40H40NS4SnI4\",\n        \"group\": \"(4Tm)2SnI4, I16Sn4\\u201a\\u00c4\\u00a28(C20H20NS4), Bis(2-(3\\u201a\\u00c4\\u00f9, 4\\u201a\\u00c4\\u00f4-dimethyl-[2,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f4,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f9,2\\u201a\\u00c4\\u00f9\\u201a\\u00c4\\u00f4-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Stable Lead-Free Perovskite Field-Effect Transistors Incorporating Linear \\u03c0\\u2010Conjugated Organic Ligands\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15577\",\n        \"pages_end\": \"15585\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate, Pd2(dba)3, P(o-tol)\\u00ac3, tributyl(3,3\\u201d-dimethyl-[2,2\\u2019:5\\u2019,2\\u201d-terthiophen]-5-yl)stannane\",\n        \"synthesis_product\": \"thin, dark red/black plate-like crystals\",\n        \"synthesis_description\": \"The organic salt 4Tm-Boc was synthesized first by mixing tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate (612 mg, 2 mmol), Pd2(dba)3 (37 mg, 2 mol%), P(o-tol)\\u00ac3 (49 mg, 8 mol%) and tributyl(3,3\\u201d-dimethyl-[2,2\\u2019:5\\u2019,2\\u201d-terthiophen]-5-yl)stannane (2.2 mmol) in a 100 mL Schlenk tube. The air was then replaced with argon, and toluene (20 mL) was added to the mixture. The mixture was stirred for 0.5 hours at 100\\u00ba C, cooled to room temperature, water was added, and the solution was extracted via dichloromethane (DCM). The organic layers were combined, washed, and dried. \\r\\n\\r\\nNext, 4Tm-Boc (1 mmol) was dissolved in 20 mL methanol, aqueous HI solution was added, and the solution was stirred for 6 hours. Solid 4TmI salt resulted.\\r\\n\\r\\nSingle crystals of (4Tm)2SnI4 were obtained by dissolving stoichiometric amounts of 4TmI and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene. This yielded thin dark red/black plates.\",\n        \"experimental_method\": \"Single-crystal X-Ray Diffraction\",\n        \"experimental_description\": \"A Bruker Quest diffractometer with kappa geometry, I-\\u03bc-S microsource X-ray tube (Cu K\\u03b1 radiation, \\u03bb = 1.54178 \\u00c5), Photon2 CMOS area detector, and multilayer mirror for monochromatization was used. Data was scanned and corrected with APEX3, space groups were solved using XPREP in SHELXTL\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06276\",\n        \"dataset_ID\": 942,\n        \"id\": 245,\n        \"compound_name\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"formula\": \"C40H40NS4SnI4\",\n        \"group\": \"(4Tm)2SnI4, I16Sn4\\u201a\\u00c4\\u00a28(C20H20NS4), Bis(2-(3\\u201a\\u00c4\\u00f9, 4\\u201a\\u00c4\\u00f4-dimethyl-[2,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f4,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f9,2\\u201a\\u00c4\\u00f9\\u201a\\u00c4\\u00f4-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP version 5.4.4\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"4x4x2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Stable Lead-Free Perovskite Field-Effect Transistors Incorporating Linear \\u03c0\\u2010Conjugated Organic Ligands\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15577\",\n        \"pages_end\": \"15585\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06276\",\n        \"dataset_ID\": 943,\n        \"id\": 245,\n        \"compound_name\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"formula\": \"C40H40NS4SnI4\",\n        \"group\": \"(4Tm)2SnI4, I16Sn4\\u201a\\u00c4\\u00a28(C20H20NS4), Bis(2-(3\\u201a\\u00c4\\u00f9, 4\\u201a\\u00c4\\u00f4-dimethyl-[2,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f4,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f9,2\\u201a\\u00c4\\u00f9\\u201a\\u00c4\\u00f4-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Stable Lead-Free Perovskite Field-Effect Transistors Incorporating Linear \\u03c0\\u2010Conjugated Organic Ligands\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15577\",\n        \"pages_end\": \"15585\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate, Pd2(dba)3, P(o-tol)\\u00ac3, tributyl(3,3\\u201d-dimethyl-[2,2\\u2019:5\\u2019,2\\u201d-terthiophen]-5-yl)stannane\",\n        \"synthesis_product\": \"film\",\n        \"synthesis_description\": \"The organic salt 4Tm-Boc was synthesized first by mixing tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate (612 mg, 2 mmol), Pd2(dba)3 (37 mg, 2 mol%), P(o-tol)\\u00ac3 (49 mg, 8 mol%) and tributyl(3,3\\u201d-dimethyl-[2,2\\u2019:5\\u2019,2\\u201d-terthiophen]-5-yl)stannane (2.2 mmol) in a 100 mL Schlenk tube. The air was then replaced with argon, and toluene (20 mL) was added to the mixture. The mixture was stirred for 0.5 hours at 100\\u00ba C, cooled to room temperature, water was added, and the solution was extracted via dichloromethane (DCM). The organic layers were combined, washed, and dried. Next, 4Tm-Boc (1 mmol) was dissolved in 20 mL methanol, aqueous HI solution was added, and the solution was stirred for 6 hours. Solid 4TmI salt resulted. Single crystals of (4Tm)2SnI4 were obtained by dissolving stoichiometric amounts of 4TmI and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene. This yielded thin dark red/black plates.\\r\\n\\r\\n4TmI (53.0 mg, 100 \\u03bcmol) and SnI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 1 mL of anhydrous DMF/DMSO (10/1) at 70 degrees C. The (4Tm)2SnI4 solution was allowed to cool to room temperature and was spin coated at 4000 rpm for 60 s on clean Si/SiO2 wafers or quartz slides. The films were annealed at 180 degrees C on a hot plate for 10 min in nitrogen.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06276\",\n        \"dataset_ID\": 944,\n        \"id\": 245,\n        \"compound_name\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"formula\": \"C40H40NS4SnI4\",\n        \"group\": \"(4Tm)2SnI4, I16Sn4\\u201a\\u00c4\\u00a28(C20H20NS4), Bis(2-(3\\u201a\\u00c4\\u00f9, 4\\u201a\\u00c4\\u00f4-dimethyl-[2,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f4,2\\u201a\\u00c4\\u00f4:5\\u201a\\u00c4\\u00f9,2\\u201a\\u00c4\\u00f9\\u201a\\u00c4\\u00f4-quarter-thiophen]-5-yl)ethan-1-ammonium) tetraiodostannate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis(2-(3\\u201d, 4\\u2019-dimethyl-[2,2\\u2019:5\\u2019,2\\u2019:5\\u201d,2\\u201d\\u2019-quarter-thiophen]-5-yl)ethan-1-ammonium) tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Stable Lead-Free Perovskite Field-Effect Transistors Incorporating Linear \\u03c0\\u2010Conjugated Organic Ligands\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15577\",\n        \"pages_end\": \"15585\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate, Pd2(dba)3, P(o-tol)\\u00ac3, tributyl(3,3\\u201d-dimethyl-[2,2\\u2019:5\\u2019,2\\u201d-terthiophen]-5-yl)stannane\",\n        \"synthesis_product\": \"film\",\n        \"synthesis_description\": \"The organic salt 4Tm-Boc was synthesized first by mixing tert-Butyl(2-(5-bromothiophen-2-yl)ethyl)carbamate (612 mg, 2 mmol), Pd2(dba)3 (37 mg, 2 mol%), P(o-tol)\\u00ac3 (49 mg, 8 mol%) and tributyl(3,3\\u201d-dimethyl-[2,2\\u2019:5\\u2019,2\\u201d-terthiophen]-5-yl)stannane (2.2 mmol) in a 100 mL Schlenk tube. The air was then replaced with argon, and toluene (20 mL) was added to the mixture. The mixture was stirred for 0.5 hours at 100\\u00ba C, cooled to room temperature, water was added, and the solution was extracted via dichloromethane (DCM). The organic layers were combined, washed, and dried. Next, 4Tm-Boc (1 mmol) was dissolved in 20 mL methanol, aqueous HI solution was added, and the solution was stirred for 6 hours. Solid 4TmI salt resulted. Single crystals of (4Tm)2SnI4 were obtained by dissolving stoichiometric amounts of 4TmI and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene. This yielded thin dark red/black plates. 4TmI (53.0 mg, 100 \\u03bcmol) and SnI2 (23.0 mg, 50 \\u03bcmol) were dissolved in 1 mL of anhydrous DMF/DMSO (10/1) at 70 degrees C. The (4Tm)2SnI4 solution was allowed to cool to room temperature and was spin coated at 4000 rpm for 60 s on clean Si/SiO2 wafers or quartz slides. The films were annealed at 180 degrees C on a hot plate for 10 min in nitrogen.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Obtained using an Agilent UV-Vis-NIR Cary-5000 spectrometer in transmission mode.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsaem.8b01809\",\n        \"dataset_ID\": 948,\n        \"id\": 246,\n        \"compound_name\": \"Hexane-1,6-diammonium bismuth iodide\",\n        \"formula\": \"C6H18N2BiI5\",\n        \"group\": \"(HDA)BiI5, C6H18BiI5N2, hexane-1,6-diaminium pentaiodo bismuthate(III)\",\n        \"organic\": \"C6H18N2\",\n        \"inorganic\": \"BiI5, Bismuth iodide\",\n        \"iupac\": \"hexane-1,6-diaminium bismuth iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of One Specific Carbon\\u2013Carbon Bond on the Quality, Stability, and Photovoltaic Performance of Hybrid Organic\\u2013Inorganic Bismuth Iodide Materials\",\n        \"journal\": \"ACS Applied Energy Materials\",\n        \"vol\": \"2\",\n        \"pages_start\": \"1579\",\n        \"pages_end\": \"1587\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"HDAI2, BiI3, DCM, DMF, DMSO\",\n        \"synthesis_product\": \"Red single crystals\",\n        \"synthesis_description\": \"Single crystals of (HDA2+)BiI5 were grown by vapor diffusion of dichloromethane (DCM) into a 0.5 M solution of 1:1 molar ratio hexane-1,6-diamine dihydriodide (HDAI2):BiI3 in a solvent mixture of 4:1 (volume ratio) N,N-dimethylformamide (DMF):dimethyl sulfoxide (DMSO), and with HDAI2 in slight excess to ensure there was no residual BiI3.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"XRD measurements made by a Bruker SMART APEX II diffractometer. The APEX2 program packages was used to determine unit-cell parameters and for data collection. Raw frame data was process with SAINT and SADABS for the reflection data file, and further calculations were performed with the SHELXTL program.\",\n        \"physical_property\": \"128.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsaem.8b01809\",\n        \"dataset_ID\": 949,\n        \"id\": 247,\n        \"compound_name\": \"Tris(N-propylammonium) bismuth iodide\",\n        \"formula\": \"C12H36N3Bi2I9\",\n        \"group\": \"(PA)3Bi2I9, N-propylammonium bismuth iodide, tris(N-propane-1-aminium) nonaiodobismuthate(III)\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"tris(N-propane-1-aminium) bismuth iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of One Specific Carbon\\u2013Carbon Bond on the Quality, Stability, and Photovoltaic Performance of Hybrid Organic\\u2013Inorganic Bismuth Iodide Materials\",\n        \"journal\": \"ACS Applied Energy Materials\",\n        \"vol\": \"2\",\n        \"pages_start\": \"1579\",\n        \"pages_end\": \"1587\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PAI, BiI3, DCM, CH3OH\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"Single crystals of (PA+)xBiI3+x were grown by vapor diffusion of dichloromethane (DCM) into a 0.5 M solution of 2:1 molar ratio n-propylamine hydriodide (PAI):BiI3 in methanol, with PAI in slight excess to ensure there was no residual BiI3. For single-crystal growth of (PA+)xBiI3+x, methanol (CH3OH) was chosen as the solvent because single crystals grown in a solvent mixture of 4:1 (v/v) DMF:DMSO were not large enough for single-crystal diffraction measurements.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"XRD measurements made by a Bruker SMART APEX II diffractometer. The APEX2 program packages was used to determine unit-cell parameters and for data collection. Raw frame data was process with SAINT and SADABS for the reflection data file, and further calculations were performed with the SHELXTL program.\",\n        \"physical_property\": \"88.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 950,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1949\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Diffuse reflectance spectra\",\n        \"experimental_description\": \"Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used. The reflectance was converted to absorbance.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 951,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1950\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Photoluminescence spectra\",\n        \"experimental_description\": \"A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the powder films to measure photoluminescence spectra. Excitation was perpendicular to the sample and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 952,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, butylammonium iodide, anhydrous acetonitrile\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \\r\\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"An Agilent Carry 60 UV-vis instrument was used in transmission mode to measure the absorbance. A blank glass substrate was used as the baseline.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 953,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, butylammonium iodide, anhydrous acetonitrile\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \\r\\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 954,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste.\\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 955,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste. \\r\\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 956,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste. \\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 957,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate, anhydrous acetonitrile\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. The solutions are combined and stirred until a red solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. It was then re-dispersed in hexane and centrifuged again to obtain the final paintlike paste. \\r\\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"An Agilent Carry 60 UV-vis instrument was used in transmission mode to measure the absorbance. A blank glass substrate was used as the baseline.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 958,\n        \"id\": 249,\n        \"compound_name\": \"Bis(benzylammonium) formmamidinium lead iodide\",\n        \"formula\": \"(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(benzylaminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 959,\n        \"id\": 249,\n        \"compound_name\": \"Bis(benzylammonium) formmamidinium lead iodide\",\n        \"formula\": \"(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(benzylaminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate, anhydrous acetonitrile\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \\r\\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"An Agilent Carry 60 UV-vis instrument was used in transmission mode to measure the absorbance. A blank glass substrate was used as the baseline.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 961,\n        \"id\": 249,\n        \"compound_name\": \"Bis(benzylammonium) formmamidinium lead iodide\",\n        \"formula\": \"(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(benzylaminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate, anhydrous acetonitrile\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \\r\\nThe solid material was dissolved in acetonitrile to a desired concentration and then was spin-coated onto a glass substrate at 3000 rpm for 30 seconds.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 962,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"TEST\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06276\",\n        \"dataset_ID\": 965,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Stable Lead-Free Perovskite Field-Effect Transistors Incorporating Linear \\u03c0\\u2010Conjugated Organic Ligands\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15577\",\n        \"pages_end\": \"15585\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"phenylethylammonium iodide (PEAI), tin (II) iodide (SnI2), gamma-bytrolactone (GBL)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Single crystals of were obtained by dissolving stoichiometric amounts of the organic salt and SnI2 in gamma-bytrolactone (GBL) (0.1 M), and then performing vapor diffusion of chloroform and chlorobenzene.\",\n        \"experimental_method\": \"Single-crystal X-Ray Diffraction\",\n        \"experimental_description\": \"A Bruker Quest diffractometer with kappa geometry, I-\\u03bc-S microsource X-ray tube (Cu K\\u03b1 radiation, \\u03bb = 1.54178 \\u00c5), Photon2 CMOS area detector, and multilayer mirror for monochromatization was used. Data was scanned and corrected with APEX3, space groups were solved using XPREP in SHELXTL\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41586-020-2219-7\",\n        \"dataset_ID\": 968,\n        \"id\": 250,\n        \"compound_name\": \"Bis(ethylammoniumbithiophene) tin iodide\",\n        \"formula\": \"(2T)2SnI4\",\n        \"group\": \"(2T)2SnI4, bis(ethylammoniumbithiophene) tetraiodostannate(II)\",\n        \"organic\": \"C5H7NS\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(ethylammoniumbithiophene) tin iodide\",\n        \"last_update\": \"2022-06-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-dimensional halide perovskite lateral epitaxial heterostructures\",\n        \"journal\": \"Nature\",\n        \"vol\": \"580\",\n        \"pages_start\": \"614\",\n        \"pages_end\": \"620\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"2T\\u2022HI(2T: bithiophenylethylammonium), tin iodide (SnI2), dimethylformide (DMF), anhydrous chlorobenzene (CB), SiO2 (300 nm)/Si substrates\",\n        \"synthesis_product\": \"<5 layers thick crystal\",\n        \"synthesis_description\": \"The process was carried out inside an N2-filled glovebox. 10 \\u03bcmol of SnI2 and 20 \\u03bcmol of 2T.HI were dissolved in 2 ml of DMF/CB co-solvent (1:1 v/v). The stock solution was then diluted 120 times by CB/AN/DCB co-solvent (2.5:1:0.01 volume ratio). 5\\u201310 \\u03bcl of the diluted solution was added onto the pre-cleaned substrate. CB vapor was allowed to be diffused at 70 \\u00b0C for 10-30 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The PL spectrum was recorded using the SpectraPro HRS-300 spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41586-020-2219-7\",\n        \"dataset_ID\": 972,\n        \"id\": 218,\n        \"compound_name\": \"Bis(ethylammoniumbithiophene) lead iodide\",\n        \"formula\": \"C20H24N2S4PbI4\",\n        \"group\": \"(2T)2PbI4, (C10H12NS2)2PbI4, bis(5-ethanaminium-2,2'-bithiophene) tetraiodoplumbate(II)\",\n        \"organic\": \"C10H12NS2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-ethanaminium-2,2'-bithiophene) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-dimensional halide perovskite lateral epitaxial heterostructures\",\n        \"journal\": \"Nature\",\n        \"vol\": \"580\",\n        \"pages_start\": \"614\",\n        \"pages_end\": \"620\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"2T\\u2022HI(2T: bithiophenylethylammonium), lead iodide (PbI2), dimethylformide (DMF), anhydrous chlorobenzene (CB)\",\n        \"synthesis_product\": \"sheet-like crystals\",\n        \"synthesis_description\": \"10 \\u03bcmol of PbI2 and 20 \\u03bcmol of 2T\\u2022HI were dissolved in 2 mL of DMF/CB co-solvent (1:1 ration). This resulted in 5 mM of stock solution. This solution was diluted 120 times by CB/An/DCB cosolvent (9.5:1:0.01 volume ratio). Only 5-10 \\u03bcmol was placed on a growth substrate SiO2, at the bottom of a glass vial and was later transferred to another vial with 3 mL of CB. This was placed on a 70\\u00ba hot plate. Growth took 10-30 minutes.\",\n        \"experimental_method\": \"Single Crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Bruker AXS D8 Quest CMOS diffractometer with kappa geometry, an I-\\u03bc-S microsource X-ray tube, multilayer G\\u00f6bel mirror, and Photon2 CMOS was used. Data was collected with Cu K\\u03b1 radiation (\\u03bb = 1.54178 \\u00c5).\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41586-020-2219-7\",\n        \"dataset_ID\": 973,\n        \"id\": 251,\n        \"compound_name\": \"Bis(bithiophenylethylammonium) lead bromide\",\n        \"formula\": \"Br8Pb2\\u20224(C10H12NS2)\",\n        \"group\": \"(2T)2PbBr4, bis(bithiophenylethylammonium) tetrabromoplumbate(II)\",\n        \"organic\": \"C5H7NS\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(bithiophenylethylammonium) lead (II) bromide\",\n        \"last_update\": \"2022-06-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-dimensional halide perovskite lateral epitaxial heterostructures\",\n        \"journal\": \"Nature\",\n        \"vol\": \"580\",\n        \"pages_start\": \"614\",\n        \"pages_end\": \"620\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"2T\\u2022HBr (2T: bithiophenylethylammonium), lead bromide (PbBr2), dimethylformide (DMF), anhydrous chlorobenzene (CB)\",\n        \"synthesis_product\": \"sheet-like crystals\",\n        \"synthesis_description\": \"10 \\u03bcmol of PbBr2 and 20 \\u03bcmol of 2T\\u2022HBr were dissolved in 2 mL of DMF/CB co-solvent (1:1 ratio). This resulted in 5 mM of stock solution. This solution was diluted 120 times by CB/An/DCB cosolvent (2.5:1:0.01 volume ratio). Only 5-10 \\u03bcmol was placed on a growth substrate SiO2, at the bottom of a glass vial and was later transferred to another vial with 3 mL of CB. This was placed on a 70\\u00ba hot plate. Growth took 10-30 minutes.\",\n        \"experimental_method\": \"Single Crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Bruker AXS D8 Quest CMOS diffractometer with kappa geometry, an I-\\u03bc-S microsource X-ray tube, multilayer G\\u00f6bel mirror, and Photon2 CMOS was used. Data was collected with Cu K\\u03b1 radiation (\\u03bb = 1.54178 \\u00c5).\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41586-020-2219-7\",\n        \"dataset_ID\": 974,\n        \"id\": 219,\n        \"compound_name\": \"Bis(ethylammoniumdimethylquaterthiophene) lead iodide\",\n        \"formula\": \"C40H40N2S8PbI4\",\n        \"group\": \"(4Tm)2PbI4, (C20H20NS4)2PbI4, 2(C20H20NS4) \\u00ac\\u2211I3Pb\\u00ac\\u2211I, 5-ethanaminium-4',3'''dimethyl-2,2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2:5\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2,2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2\\u201a\\u00c4\\u00f2-quaterthiophene tetraiodoplumbate(II)\",\n        \"organic\": \"C20H20NS4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5-ethanaminium-4',3'''dimethyl-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tin iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-dimensional halide perovskite lateral epitaxial heterostructures\",\n        \"journal\": \"Nature\",\n        \"vol\": \"580\",\n        \"pages_start\": \"614\",\n        \"pages_end\": \"620\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"4Tm\\u2022HI(4Tm: quaterthiophenylethylammonium), lead iodide (PbI2), dimethylformide (DMF), anhydrous chlorobenzene (CB)\",\n        \"synthesis_product\": \"sheet-like crystals\",\n        \"synthesis_description\": \"10 \\u03bcmol of PbI2 and 20 \\u03bcmol of 4Tm\\u2022HI were dissolved in 2 mL of DMF/CB co-solvent (1:1 ration). This resulted in 5 mM of stock solution. This solution was diluted 240 times by CB/An/DCB cosolvent (3.9:1:0.01 volume ratio). Only 5-10 \\u03bcmol was placed on a growth substrate SiO2, at the bottom of a glass vial and was later transferred to another vial with 3 mL of CB. This was placed on a 90\\u00ba hot plate. Growth took 10-30 minutes.\",\n        \"experimental_method\": \"Single Crystal X-Ray Diffraction\",\n        \"experimental_description\": \"Bruker AXS D8 Quest CMOS diffractometer with kappa geometry, an I-\\u03bc-S microsource X-ray tube, multilayer G\\u00f6bel mirror, and Photon2 CMOS was used. Data was collected with Cu K\\u03b1 radiation (\\u03bb = 1.54178 \\u00c5).\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 978,\n        \"id\": 64,\n        \"compound_name\": \"Bis(butylammonium) lead bromide\",\n        \"formula\": \"C8H24N2PbBr4\",\n        \"group\": \"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(butyl-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            981\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), PbBr2, HBr\",\n        \"synthesis_product\": \"Colorless single crystals\",\n        \"synthesis_description\": \"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 979,\n        \"id\": 252,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2CsPb2Br7\",\n        \"group\": \"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"CsPb2Br7, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            982\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 980,\n        \"id\": 253,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2Cs2Pb3Br10\",\n        \"group\": \"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"Cs2Pb3Br10, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            983\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 981,\n        \"id\": 64,\n        \"compound_name\": \"Bis(butylammonium) lead bromide\",\n        \"formula\": \"C8H24N2PbBr4\",\n        \"group\": \"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(butyl-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            978\n        ],\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), PbBr2, HBr\",\n        \"synthesis_product\": \"Colorless single crystals\",\n        \"synthesis_description\": \"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 982,\n        \"id\": 252,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2CsPb2Br7\",\n        \"group\": \"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"CsPb2Br7, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            979\n        ],\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 983,\n        \"id\": 253,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2Cs2Pb3Br10\",\n        \"group\": \"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"Cs2Pb3Br10, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            980\n        ],\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3101 UV-vis spectrophotometer was used to measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 987,\n        \"id\": 64,\n        \"compound_name\": \"Bis(butylammonium) lead bromide\",\n        \"formula\": \"C8H24N2PbBr4\",\n        \"group\": \"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(butyl-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            990\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), PbBr2, HBr\",\n        \"synthesis_product\": \"Colorless single crystals\",\n        \"synthesis_description\": \"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 988,\n        \"id\": 252,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2CsPb2Br7\",\n        \"group\": \"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"CsPb2Br7, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            991\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 989,\n        \"id\": 253,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2Cs2Pb3Br10\",\n        \"group\": \"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"Cs2Pb3Br10, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            992\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 990,\n        \"id\": 64,\n        \"compound_name\": \"Bis(butylammonium) lead bromide\",\n        \"formula\": \"C8H24N2PbBr4\",\n        \"group\": \"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(butyl-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            987\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), PbBr2, HBr\",\n        \"synthesis_product\": \"Colorless single crystals\",\n        \"synthesis_description\": \"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 991,\n        \"id\": 252,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2CsPb2Br7\",\n        \"group\": \"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"CsPb2Br7, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            988\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"PL spectra were recorded in a PL microscope. A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used for the measurements.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 992,\n        \"id\": 253,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2Cs2Pb3Br10\",\n        \"group\": \"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"Cs2Pb3Br10, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            989\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr, CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2Csn-1PbBr3n+1 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution in an appropriate stoichiometry. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling to room temperature colorless (n = 1) and yellow (n = 2 and 3) precipitated in their respective solutions. The crystals were removed by suctio9n filtration and were dried in a vacuum. Pure-phase single crystals were obtained via the following BA:Cs:Pb ratios: n = 1, 2:0:1; n = 2, 3:1:2, n = 3, 3.5:2:3.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Janish Research Company ST-500 microscope cryostat using a Coherent OBIS 375LX laser was used to measure low-temperature PL. An excitation wavelength of 375 nm was used. PL spectra at high temperature was performed in the same system with a HCP422G gas-tight hot plate.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 995,\n        \"id\": 64,\n        \"compound_name\": \"Bis(butylammonium) lead bromide\",\n        \"formula\": \"C8H24N2PbBr4\",\n        \"group\": \"bis(butyl-1-aminium) tetrabromoplumbate(II), (BA)2PbBr4, (C4H12N)2PbBr4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(butyl-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), PbBr2, HBr\",\n        \"synthesis_product\": \"Colorless single crystals\",\n        \"synthesis_description\": \"(BA)2PbBr4 crystals were synthesized by mixing BABr, and PbBr2 into a saturated HBr solution at a molar ratio of 2:1. Complete dissolution was achieved by heating to boiling with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 1\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A synchrotron radiation source ( \\u03bb = 0.7749 \\u00c5) in a nitrogen atmosphere was used for the SCXRD data. The crystals were mounted on a Bruker diffractometer using a Kapton tip. Nitrogen cryogen with a temperature controller precisely adjusted the temperature during measurement. APEX 3 software was used for data reduction and SADABS software was used for multiscan absorption correction. Structure calculations were performed using the SHELXTL program.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 998,\n        \"id\": 253,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2Cs2Pb3Br10\",\n        \"group\": \"(BA)2Cs2Pb3Br10, bis(butane-1-aminium) dicaesium decabromo triplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"Cs2Pb3Br10, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2Cs2Pb3Br10 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3.5:2:3. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A synchrotron radiation source ( \\u03bb = 0.7749 \\u00c5) in a nitrogen atmosphere was used for the SCXRD data.  The crystals were mounted on a Bruker diffractometer with a Kapton tip. Nitrogen cryogen with a temperature controller precisely adjusted the temperature during measurement. APEX 3 software was used for data reduction and SADABS software was used for multiscan absorption correction. Structure calculations were performed using the SHELXTL program.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay4045\",\n        \"dataset_ID\": 999,\n        \"id\": 252,\n        \"compound_name\": \"Bis(butylammonium) caesium lead bromide\",\n        \"formula\": \"C8H24N2CsPb2Br7\",\n        \"group\": \"(BA)2CsPb2Br7, bis(butane-1-aminium) caesium septabromo diplumbate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"CsPb2Br7, Caesium lead bromide\",\n        \"iupac\": \"bis(butane-1-aminium) caesium lead bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and spectral dynamics of single-crystalline Ruddlesden-Popper phase halide perovskite blue light-emitting diodes\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"6\",\n        \"pages_start\": \"eaay4045\",\n        \"pages_end\": \"eaay4045\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"BABr (synthesized), CsBr, PbBr2, HBr\",\n        \"synthesis_product\": \"Yellow single crystals\",\n        \"synthesis_description\": \"(BA)2CsPb2Br7 crystals were synthesized by mixing BABr, CsBr, and PbBr2 into a saturated HBr solution at a molar ratio of 3:1:2. Complete dissolution was achieved by heating to 100\\u00b0C with constant stirring for ~30 minutes. Upon slowly cooling, at a rate of 20\\u00b0C/min to room temperature, the crystals precipitated. The crystals were removed by suction filtration and were dried in a vacuum.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A synchrotron radiation source ( \\u03bb = 0.7749 \\u00c5) in a nitrogen atmosphere was used for the SCXRD data. The crystals were mounted on a Bruker diffractometer using a Kapton tip. Nitrogen cryogen with a temperature controller precisely adjusted the temperature during measurement. APEX 3 software was used for data reduction and SADABS software was used for multiscan absorption correction. Structure calculations were performed using the SHELXTL program.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/b606987h\",\n        \"dataset_ID\": 1002,\n        \"id\": 216,\n        \"compound_name\": \"bismethylbenzylammonium lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"(MBA)2PbI4, \\u0152\\u00b1-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bismethylbenzylaminium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"Chiral 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and crystal structures of inorganic\\u2013organic hybrids incorporating an aromatic amine with a chiral functional group\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"8\",\n        \"pages_start\": \"686\",\n        \"pages_end\": \"695\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbO, (R/S)-MBA ((R/S)-methylbenzylamine / (R/S)-1-phenylethylamine), HI\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"PbO and R- or S-C6H5C2H4NH2 were added to HI. The solution fully dissolved after refluxing at 100 degrees Celsius for 3 hours. It was then cooled slowly over four days, over which time orange crystals began precipitating below 60 degrees.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer was used with monocrhomated Mo Kalpha radiation. Omega-scans of width 0.3 degrees were used to collect the data, and data reduction was performed with the SAINT+ program, version 6.02. Face indexed absorption corrections were performed with the XPREP program. The crystal structure was solved at -100 degrees Celsius using the SHELXS-97 program.\",\n        \"physical_property\": \"173.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"(R-MBA)2PbI4\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"Manually from the article\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay0571\",\n        \"dataset_ID\": 1003,\n        \"id\": 216,\n        \"compound_name\": \"bismethylbenzylammonium lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"(MBA)2PbI4, \\u0152\\u00b1-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bismethylbenzylaminium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"Chiral 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Spin-dependent charge transport through 2D chiral hybrid lead-iodide perovskites\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"5\",\n        \"pages_start\": \"eaay0571\",\n        \"pages_end\": \"eaay0571\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"DMF, lead oxide (PbO, 99.999%), (\\u00b1)-\\u03b1-methylbenzylamine (rac-MBA, 99%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"200 mg of PbO (0.897 mmol), 200 \\u03bcl (1.57 mmol) of rac-MBA were dissolved in 6 ml of HI by heating at 90\\u00b0C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1\\u00b0C/hour. The obtained crystals were filtered and washed with diethyl ether.\\r\\nThe crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto quartz substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100\\u00b0C for 10 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay0571\",\n        \"dataset_ID\": 1005,\n        \"id\": 216,\n        \"compound_name\": \"bismethylbenzylammonium lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"(MBA)2PbI4, \\u0152\\u00b1-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bismethylbenzylaminium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"Chiral 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"circular dichroism (CD)\",\n        \"primary_unit\": \"mDegree\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Spin-dependent charge transport through 2D chiral hybrid lead-iodide perovskites\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"5\",\n        \"pages_start\": \"eaay0571\",\n        \"pages_end\": \"eaay0571\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"DMF, lead oxide (PbO, 99.999%), (R)-(+)-\\u03b1-methylbenzylamine (R-MBA, 98%, ee 96%), (S)-(\\u2212)-\\u03b1-methylbenzylamine (S-MBA, 98%, ee 98%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"200 mg of PbO (0.897 mmol), 200 \\u03bcl (1.57 mmol) of R-, S-MBA were dissolved in 6 ml of HI by heating at 90\\u00b0C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1\\u00b0C/hour. The obtained crystals were filtered and washed with diethyl ether. The crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto quartz substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100\\u00b0C for 10 min.\",\n        \"experimental_method\": \"Circular Dichroism (CD) Spectroscopy\",\n        \"experimental_description\": \"A Jasco J-715 spectropolarimeter was used on thin film samples. Spectra were averaged over five scans. An internal algorithm in the Jasco software package was used to smooth the spectra. CD spectra were taken from 200 to 600 nm at 0.2-nm resolution.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"(R-MBA)2PbI4\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.7b02322\",\n        \"dataset_ID\": 1006,\n        \"id\": 241,\n        \"compound_name\": \"bis(methylammonium) potassium gadolinium chloride\",\n        \"formula\": \"C2H12N2KGdCl6\",\n        \"group\": \"(MA)2KGdCl6, (CH3NH3)2KGdCl6, bis(methanaminium) trichlorogadoliniate(III) tripotassiate(I)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"KGdCl6, Potassium chloride gadolinium\",\n        \"iupac\": \"bis(methanaminium) potassium gadolinium chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Characterization of the Rare-Earth Hybrid Double Perovskites: (CH3NH3)2KGdCl6 and (CH3NH3)2KYCl6\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5020\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Gd2O3, KCl, (MA)Cl, HCl\",\n        \"synthesis_product\": \"Colorless single crystals\",\n        \"synthesis_description\": \"Y2O3 or Gd2O3, KCL, and (MA)Cl were dissolved in an HCl solution inside a capped glass vial. It was held at 80 degrees Celsius and stirred for one hour, becoming clear and colorless. The cap was opened, and the solution was evaporated at 85 degrees leaving behind crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an Xcalibur/Gemini Ultra diffractometer and an Eos CCD area detector.\",\n        \"physical_property\": \"300.0 (\\u00b10.14)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201811497\",\n        \"dataset_ID\": 1007,\n        \"id\": 254,\n        \"compound_name\": \"Benzodiimidazolium tin iodide\",\n        \"formula\": \"C8H8N4SnI4\",\n        \"group\": \"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",\n        \"organic\": \"C8H8N4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead and HTM Free Stable Two-Dimensional Tin Perovskites with Suitable Band Gap for Solar Cell Applications\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"58\",\n        \"pages_start\": \"1072\",\n        \"pages_end\": \"1076\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Benzodiimidazole, ethanol, HI, SnI2\",\n        \"synthesis_product\": \"Black plate-like crystals\",\n        \"synthesis_description\": \"Benzodiimdazole was suspended in ethanol and then HI was added. The solution was refluxed for 1 hour and was then cooled to room temperature, during which solid benzodiimedazolium iodide salt precipitated. The solid were collected and were used to start the process another three times to ensure full protonation. They were then washed with ethanol and dried in vacuum to obtain an off-white solid. The perovskite was then obtained by heating stoichiometric amounts of the iodide salt with tin or lead iodide in an HI solution for 1 day before cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker D8 Venture diffractometer with Mo Kalpha radiation was used. SAINT and SADABS in the APEX 3 software package was used for data reduction and absorption correction. The structure was solved using SHELXS and further refinement using SHELXL-2014 in the WINGX environment.\",\n        \"physical_property\": \"300.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201811497\",\n        \"dataset_ID\": 1008,\n        \"id\": 254,\n        \"compound_name\": \"Benzodiimidazolium tin iodide\",\n        \"formula\": \"C8H8N4SnI4\",\n        \"group\": \"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",\n        \"organic\": \"C8H8N4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1011\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead and HTM Free Stable Two-Dimensional Tin Perovskites with Suitable Band Gap for Solar Cell Applications\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"58\",\n        \"pages_start\": \"1072\",\n        \"pages_end\": \"1076\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",\n        \"synthesis_product\": \"film on glass\",\n        \"synthesis_description\": \"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 \\u03bcl chlorobenzene was added. The film was annealed at 100 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Absorption measurements were performed using Perkin Elmer Lambda 950S equipped with an integrating sphere.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201811497\",\n        \"dataset_ID\": 1009,\n        \"id\": 254,\n        \"compound_name\": \"Benzodiimidazolium tin iodide\",\n        \"formula\": \"C8H8N4SnI4\",\n        \"group\": \"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",\n        \"organic\": \"C8H8N4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1010\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead and HTM Free Stable Two-Dimensional Tin Perovskites with Suitable Band Gap for Solar Cell Applications\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"58\",\n        \"pages_start\": \"1072\",\n        \"pages_end\": \"1076\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",\n        \"synthesis_product\": \"film on glass\",\n        \"synthesis_description\": \"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 \\u03bcl chlorobenzene was added. The film was annealed at 100 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was obtained using a Fluorescence Spectrometer LS 55 from PerkinElmer\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201811497\",\n        \"dataset_ID\": 1010,\n        \"id\": 254,\n        \"compound_name\": \"Benzodiimidazolium tin iodide\",\n        \"formula\": \"C8H8N4SnI4\",\n        \"group\": \"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",\n        \"organic\": \"C8H8N4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1009\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead and HTM Free Stable Two-Dimensional Tin Perovskites with Suitable Band Gap for Solar Cell Applications\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"58\",\n        \"pages_start\": \"1072\",\n        \"pages_end\": \"1076\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",\n        \"synthesis_product\": \"film on glass\",\n        \"synthesis_description\": \"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 \\u03bcl chlorobenzene was added. The film was annealed at 100 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was obtained using a Fluorescence Spectrometer LS 55 from PerkinElmer\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201811497\",\n        \"dataset_ID\": 1011,\n        \"id\": 254,\n        \"compound_name\": \"Benzodiimidazolium tin iodide\",\n        \"formula\": \"C8H8N4SnI4\",\n        \"group\": \"BdiSnI4, Benzodiimidazolium tetraiodostannate(II)\",\n        \"organic\": \"C8H8N4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1008\n        ],\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead and HTM Free Stable Two-Dimensional Tin Perovskites with Suitable Band Gap for Solar Cell Applications\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"58\",\n        \"pages_start\": \"1072\",\n        \"pages_end\": \"1076\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"benzodiimidazolium diiodide, DMSO, DMF, chlorobenzene, SnI2\",\n        \"synthesis_product\": \"film on glass\",\n        \"synthesis_description\": \"0.5 mmol of SnI2 and 1 mmol benzodiimidazolium diiodide were dissolved in a 2:1 mixture of DMSO:DMF. The solution was spin-coated on the substrate at 5000 rpm for 30s using a ramp of 3000 rpm s-1. At 15s, 100 \\u03bcl chlorobenzene was added. The film was annealed at 100 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Absorption measurements were performed using Perkin Elmer Lambda 950S equipped with an integrating sphere. The optical band gap can be estimated from the corresponding Tauc\\u2010plot with a direct band gap assumption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201811497\",\n        \"dataset_ID\": 1012,\n        \"id\": 255,\n        \"compound_name\": \"Benzodiimidazolium lead iodide\",\n        \"formula\": \"C8H8N4PbI4\",\n        \"group\": \"BdiPbI4, Benzodiimidazolium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H8N4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3,7-dihydrobenzo[1,2-d:4,5-d']diimidazole-1,5-diium lead (II) iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead and HTM Free Stable Two-Dimensional Tin Perovskites with Suitable Band Gap for Solar Cell Applications\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"58\",\n        \"pages_start\": \"1072\",\n        \"pages_end\": \"1076\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Benzodiimidazole, ethanol, HI, PbI2\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Benzodiimdazole was suspended in ethanol and then HI was added. The solution was refluxed for 1 hour and was then cooled to room temperature, during which solid benzodiimedazolium iodide salt precipitated. The solid were collected and were used to start the process another three times to ensure full protonation. They were then washed with ethanol and dried in vacuum to obtain an off-white solid. The perovskite was then obtained by heating stoichiometric amounts of the iodide salt with tin or lead iodide in an HI solution for 1 day before cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker D8 Venture diffractometer with Mo Kalpha radiation was used. SAINT and SADABS in the APEX 3 software package was used for data reduction and absorption correction. The structure was solved using SHELXS and further refinement using SHELXL-2014 in the WINGX environment.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1013,\n        \"id\": 256,\n        \"compound_name\": \"Tris(thiophenyl) lead iodide\",\n        \"formula\": \"Pb2I(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monoiododiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2I, Lead iodide\",\n        \"iupac\": \"Tris(thiophenyl) lead iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium ioddie (MAI), N, N-dimethylformamide (DMF)\",\n        \"synthesis_product\": \"orange plate-shaped crystals\",\n        \"synthesis_description\": \"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.Pb(SC6H5)2 (107 mg) and MAI (40 mg) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95\\u00baC, at which temperature the stirring stopped and the solution was cooled at a rate of 5\\u00baC per 20 minutes until the temperature reached 40\\u00baC. The solution was left, undisturbed, overnight.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker AXS D8 Quest CMOS diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Frames were collected at 150 K with \\u03c9 and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1014,\n        \"id\": 256,\n        \"compound_name\": \"Tris(thiophenyl) lead iodide\",\n        \"formula\": \"Pb2I(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monoiododiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2I, Lead iodide\",\n        \"iupac\": \"Tris(thiophenyl) lead iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1015,\n            1018,\n            1021\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium iodide (MAI), N, N-dimethylformamide (DMF), ethanol\",\n        \"synthesis_product\": \"exfoliated crystals on silicon substrates\",\n        \"synthesis_description\": \"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.\\r\\nPb(SC6H5)2 (107 mg) and MAI (40 mg) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95\\u00baC, at which temperature the stirring stopped and the solution was cooled at a rate of 5\\u00baC per 20 minutes until the temperature reached 40\\u00baC. The solution was left, undisturbed, overnight. The crystals were washed with ethanol. Exfoliation was performed using scotch tape.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Two independent sub-picosecond excitation beams (400 nm) were generated by two optical parametric amplifiers. Beams were focused onto a sample with 40X objective, PL emission was collected with the same objective (Nikon, NA = 0.6), dispersed by a 300 mm spectrometer (Andor Tech.), and detected by a thermoelectric cooled CCD detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1015,\n        \"id\": 256,\n        \"compound_name\": \"Tris(thiophenyl) lead iodide\",\n        \"formula\": \"Pb2I(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monoiododiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2I, Lead iodide\",\n        \"iupac\": \"Tris(thiophenyl) lead iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1014,\n            1018,\n            1021\n        ],\n        \"primary_name\": \"Stokes shift\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium iodide (MAI), N, N-dimethylformamide (DMF), ethanol\",\n        \"synthesis_product\": \"exfoliated crystals on silicon substrates (for PL)\\r\\n+ thin film on quartz substrates (for absorption)\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Photoluminescence microscopy + UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1016,\n        \"id\": 256,\n        \"compound_name\": \"Tris(thiophenyl) lead iodide\",\n        \"formula\": \"Pb2I(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monoiododiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2I, Lead iodide\",\n        \"iupac\": \"Tris(thiophenyl) lead iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1017,\n        \"id\": 256,\n        \"compound_name\": \"Tris(thiophenyl) lead iodide\",\n        \"formula\": \"Pb2I(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monoiododiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2I, Lead iodide\",\n        \"iupac\": \"Tris(thiophenyl) lead iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00baC in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. \\r\\nThin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with a direct band gap assumption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1018,\n        \"id\": 256,\n        \"compound_name\": \"Tris(thiophenyl) lead iodide\",\n        \"formula\": \"Pb2I(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monoiododiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2I, Lead iodide\",\n        \"iupac\": \"Tris(thiophenyl) lead iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1014,\n            1015,\n            1021\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (!0 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1021,\n        \"id\": 256,\n        \"compound_name\": \"Tris(thiophenyl) lead iodide\",\n        \"formula\": \"Pb2I(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monoiododiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2I, Lead iodide\",\n        \"iupac\": \"Tris(thiophenyl) lead iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1014,\n            1015,\n            1018\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), N, N-dimethylformamide (DMF), lead iodide (PbI2)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbI2 in a 3:1 ratio in DMF. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1022,\n        \"id\": 257,\n        \"compound_name\": \"Tris(thiophenyl) lead bromide\",\n        \"formula\": \"Pb2Br(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monobromodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Br, Lead bromide\",\n        \"iupac\": \"Tris(thiophenyl) lead bromide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium bromide (MABr), N, N-dimethylformamide (DMF)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.Pb(SC6H5)2 (107 mg) and MABr (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95\\u00baC, at which temperature the stirring stopped and the solution was cooled at a rate of 5\\u00baC per 20 minutes until the temperature reached 40\\u00baC. The solution was left, undisturbed, overnight.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker AXS D8 Quest CMOS diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Frames were collected at 150 K with \\u03c9 and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Original file from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1023,\n        \"id\": 257,\n        \"compound_name\": \"Tris(thiophenyl) lead bromide\",\n        \"formula\": \"Pb2Br(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monobromodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Br, Lead bromide\",\n        \"iupac\": \"Tris(thiophenyl) lead bromide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead bromide (PbBr2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. \\r\\n\\r\\nThin films were created by mixing Pb(SC6H5)2 and PbBr2 in a 3:1 ratio in DMF and 0.9\\u2005mL DMSO. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra. Images were obtained via a Hitachi 4600-S scanning electron microscope\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1024,\n        \"id\": 257,\n        \"compound_name\": \"Tris(thiophenyl) lead bromide\",\n        \"formula\": \"Pb2Br(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monobromodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Br, Lead bromide\",\n        \"iupac\": \"Tris(thiophenyl) lead bromide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead bromide (PbBr2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbBr2 in a 3:1 ratio in DMF and 0.9\\u2005mL DMSO. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1025,\n        \"id\": 257,\n        \"compound_name\": \"Tris(thiophenyl) lead bromide\",\n        \"formula\": \"Pb2Br(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monobromodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Br, Lead bromide\",\n        \"iupac\": \"Tris(thiophenyl) lead bromide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium bromide (MABr), N, N-dimethylformamide (DMF), ethanol\",\n        \"synthesis_product\": \"exfoliated crystals on silicon substrates\",\n        \"synthesis_description\": \"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.\\r\\nPb(SC6H5)2 (107 mg) and MABr (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95\\u00baC, at which temperature the stirring stopped and the solution was cooled at a rate of 5\\u00baC per 20 minutes until the temperature reached 40\\u00baC. The solution was left, undisturbed, overnight.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Two independent sub-picosecond excitation beams (400 nm) were generated by two optical parametric amplifiers. Beams were focused onto a sample with 40X objective, PL emission was collected with the same objective (Nikon, NA = 0.6), dispersed by a 300 mm spectrometer (Andor Tech.), and detected by a thermoelectric cooled CCD detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1026,\n        \"id\": 257,\n        \"compound_name\": \"Tris(thiophenyl) lead bromide\",\n        \"formula\": \"Pb2Br(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monobromodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Br, Lead bromide\",\n        \"iupac\": \"Tris(thiophenyl) lead bromide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead bromide (PbBr2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbBr2 in a 3:1 ratio in DMF and 0.9\\u2005mL DMSO. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1027,\n        \"id\": 258,\n        \"compound_name\": \"Tris(thiophenyl) lead chloride\",\n        \"formula\": \"Pb2Cl(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monochlorodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Cl, Lead chloride\",\n        \"iupac\": \"Tris(thiophenyl) lead chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium chloride (MACl), N, N-dimethylformamide (DMF)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.Pb(SC6H5)2 (107 mg) and MACl (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95\\u00baC, at which temperature the stirring stopped and the solution was cooled at a rate of 5\\u00baC per 20 minutes until the temperature reached 40\\u00baC. The solution was left, undisturbed, overnight.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker AXS D8 Quest CMOS diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Frames were collected at 150 K with \\u03c9 and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Original file from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1028,\n        \"id\": 258,\n        \"compound_name\": \"Tris(thiophenyl) lead chloride\",\n        \"formula\": \"Pb2Cl(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monochlorodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Cl, Lead chloride\",\n        \"iupac\": \"Tris(thiophenyl) lead chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead chloride (PbCl2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbCl2 in a 3:1 ratio in DMF and 0.9\\u2005mL DMSO. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"A Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectra. Images were obtained via a Hitachi 4600-S scanning electron microscope\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1029,\n        \"id\": 258,\n        \"compound_name\": \"Tris(thiophenyl) lead chloride\",\n        \"formula\": \"Pb2Cl(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monochlorodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Cl, Lead chloride\",\n        \"iupac\": \"Tris(thiophenyl) lead chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead chloride (PbCl2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbCl2 in a 3:1 ratio in DMF and 0.9\\u2005mL DMSO. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1030,\n        \"id\": 258,\n        \"compound_name\": \"Tris(thiophenyl) lead chloride\",\n        \"formula\": \"Pb2Cl(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monochlorodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Cl, Lead chloride\",\n        \"iupac\": \"Tris(thiophenyl) lead chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium chloride (MACl), N, N-dimethylformamide (DMF)\",\n        \"synthesis_product\": \"exfoliated crystals on silicon substrates\",\n        \"synthesis_description\": \"A slow cooling technique was used. Lead(II) benzenethiolate (Pb(SC6H5)2) was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1 v/v) (10 mL) while being simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours.\\r\\nPb(SC6H5)2 (107 mg) and MACl (0.25 mmol*) were added to a 1.5 mL solution of DMF and 33% ethanol (etOH) (1.0 mL DMF, 0.5 mL EtOH). The solution was stirred, and heated until completely dissolved at 95\\u00baC, at which temperature the stirring stopped and the solution was cooled at a rate of 5\\u00baC per 20 minutes until the temperature reached 40\\u00baC. The solution was left, undisturbed, overnight. The crystals were washed with ethanol. Exfoliation was performed using scotch tape.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Two independent sub-picosecond excitation beams (400 nm) were generated by two optical parametric amplifiers. Beams were focused onto a sample with 40X objective, PL emission was collected with the same objective (Nikon, NA = 0.6), dispersed by a 300 mm spectrometer (Andor Tech.), and detected by a thermoelectric cooled CCD detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1031,\n        \"id\": 258,\n        \"compound_name\": \"Tris(thiophenyl) lead chloride\",\n        \"formula\": \"Pb2Cl(SC6H5)3\",\n        \"group\": \"Tris(thiophenyl) monochlorodiplumbate(II)\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Pb2Cl, Lead chloride\",\n        \"iupac\": \"Tris(thiophenyl) lead chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), lead chloride (PbCl2), N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO)\",\n        \"synthesis_product\": \"Thin-film on quartz\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (10 mL) while simultaneously heated at 70\\u00ba in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. Thin films were created by mixing Pb(SC6H5)2 and PbCl2 in a 3:1 ratio in DMF and 0.9\\u2005mL DMSO. 40 \\u03bcL of the resultant solution was spin-coated at 2000 rpm on quartz substrates, and 150 \\u03bcL of diethyl ether was dropped onto the substrate. Films were annealed in air at 100\\u00baC for 5 min.\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1032,\n        \"id\": 259,\n        \"compound_name\": \"PbI1.524(S-C6H5)0.476\",\n        \"formula\": \"PbI1.524(S-C6H5)0.476\",\n        \"group\": \"*\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"*\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead (II) acetate trihydrate (Sigma-Aldrich, 99.9%), Thiophenol (Oakwood Chemical), methylammonium iodide (MAI), ethanol, \\u03b3-butyrolactone (GBL)\",\n        \"synthesis_product\": \"dark orange, plate-shaped crystals\",\n        \"synthesis_description\": \"Pb(SC6H5)2 was synthesized directly. First, Lead (II) acetate trihydrate (258.98 mg, 2.35 mmol) was dissolved in an ethanol-water solution (4:1) (!0 mL) while being simultaneously heated at 70\\u00ba C in an oil bath and stirred. Next, Thiophenol (482.72 mL, 4.70 mmol) was mixed with ethanol (5 mL) and added dropwise to the solution, while being continuously stirred. The solution was air-dried for 1 hour afterward, and the yellow precipitate was washed. Filtered, and dried for 4 hours. \\r\\n\\r\\nSingle crystals were grown via vapor diffusion. A 1:4 molar ratio of Pb(SC6H5)2 and MAI were dissolved in \\u03b3- butyrolactone (GBL) and produced a 200 mg mL-1 solution by being heated and stirred for 1 hour.  0.3 mL was placed into a small vial, then into a larger vial with 5 mL of ethanol, and sealed for three days, at which time crystals formed.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker AXS D8 Quest CMOS diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Frames were collected at 150 K with \\u03c9 and phi scans. Multiscan methods and SADABS v 2016 corrected absorption.\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"P-3m1\",\n        \"extraction_method\": \"Original file from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/chem.201905790\",\n        \"dataset_ID\": 1033,\n        \"id\": 259,\n        \"compound_name\": \"PbI1.524(S-C6H5)0.476\",\n        \"formula\": \"PbI1.524(S-C6H5)0.476\",\n        \"group\": \"*\",\n        \"organic\": \"SC6H5\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"*\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural Tunability and Diversity of Two\\u2010Dimensional Lead Halide Benzenethiolate\",\n        \"journal\": \"Chemistry \\u2013 A European Journal\",\n        \"vol\": \"26\",\n        \"pages_start\": \"6599\",\n        \"pages_end\": \"6607\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption (transmission mode)\",\n        \"experimental_description\": \"The Cary 60 Ultraviolet-Visible light spectrophotometer was used in transmission mode to collect absorption spectrum data, and the band gap was extracted from the Tauc plot with indirect band gap assumption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1034,\n        \"id\": 260,\n        \"compound_name\": \"Guanidinium methylammonium lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)PbI4\",\n        \"group\": \"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium methanaminium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Red needle-like crystals\",\n        \"synthesis_description\": \"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until \\u223c25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"SCXRD was performed with a STOE IPDS II or IPDS 2T diffractometer using Mo Kalpha radiation working at 50 kV and 40 mA. Integration and absorption corrections were made with the X-AREA, X-RED, and X-SHAPE programs. Structures were solved via charge flipping and were refined full-matrix least squares with the Jana2006 package. PLATON software was used to identify twinning domains and to validate the space groups.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1035,\n        \"id\": 260,\n        \"compound_name\": \"Guanidinium methylammonium lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)PbI4\",\n        \"group\": \"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium methanaminium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Red needle-like crystals\",\n        \"synthesis_description\": \"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until \\u223c25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transformation was used to convert the data to absorbance.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imma\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1036,\n        \"id\": 260,\n        \"compound_name\": \"Guanidinium methylammonium lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)PbI4\",\n        \"group\": \"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium methanaminium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Red needle-like crystals\",\n        \"synthesis_description\": \"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until \\u223c25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-res confocal Ramon microscope spectrometer that was equipped with a diode CW laser (excitation wavelength 473 nm, 25 mW power) and a Synapse CCD camera was used. PL spectra were measured on the oriented crystals.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1037,\n        \"id\": 260,\n        \"compound_name\": \"Guanidinium methylammonium lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)PbI4\",\n        \"group\": \"(Gua)(MA)PbI4, (GA)(MA)PbI4, diaminomethanaminium methanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium methanaminium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Red needle-like crystals\",\n        \"synthesis_description\": \"PbO (670 mg, 3 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (203 mg, 3 mmol) and C(NH2)3Cl (287 mg, 3 mmol) were added and continued to be reflexed/stirred for a few hours until \\u223c25% of the acid solution evaporated. Then stirring was stopped and the solution was gradually cooled to room temperature, causing red crystals to precipitate. The crystals were allowed to stand for two days and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BaSO4 was used as the 100% reflectance reference, and the Kubelka-Munk transformation was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1038,\n        \"id\": 261,\n        \"compound_name\": \"Guanidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)2Pb2I7\",\n        \"group\": \"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-22\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Dark red single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"SCXRD was performed with a STOE IPDS II or IPDS 2T diffractometer using Mo Kalpha radiation working at 50 kV and 40 mA. Integration and absorption corrections were made with the X-AREA, X-RED, and X-SHAPE programs. Structures were solved via charge flipping and were refined full-matrix least squares with the Jana2006 package. PLATON software was used to identify twinning domains and to validate the space groups.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Bmm2\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1039,\n        \"id\": 261,\n        \"compound_name\": \"Guanidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)2Pb2I7\",\n        \"group\": \"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-22\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Dark red single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1040,\n        \"id\": 261,\n        \"compound_name\": \"Guanidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)2Pb2I7\",\n        \"group\": \"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-22\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Dark red single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-res confocal Ramon microscope spectrometer that was equipped with a diode CW laser (excitation wavelength 473 nm, 25 mW power) and a Synapse CCD camera was used. PL spectra were measured on the oriented crystals.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1041,\n        \"id\": 261,\n        \"compound_name\": \"Guanidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)2Pb2I7\",\n        \"group\": \"(Gua)(MA)2Pb2I7, (GA)(MA)2Pb2I7, diaminomethanaminium bis(methanaminium) septaiodo diplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-22\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Dark red single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (478 mg, 5 mmol) were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing dark red crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1042,\n        \"id\": 262,\n        \"compound_name\": \"Guanidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)3Pb3I10\",\n        \"group\": \"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Black single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"SCXRD was performed with a STOE IPDS II or IPDS 2T diffractometer using Mo Kalpha radiation working at 50 kV and 40 mA. Integration and absorption corrections were made with the X-AREA, X-RED, and X-SHAPE programs. Structures were solved via charge flipping and were refined full-matrix least squares with the Jana2006 package. PLATON software was used to identify twinning domains and to validate the space groups.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1043,\n        \"id\": 262,\n        \"compound_name\": \"Guanidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)3Pb3I10\",\n        \"group\": \"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Black single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1044,\n        \"id\": 262,\n        \"compound_name\": \"Guanidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)3Pb3I10\",\n        \"group\": \"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Black single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-res confocal Ramon microscope spectrometer that was equipped with a diode CW laser (excitation wavelength 473 nm, 25 mW power) and a Synapse CCD camera was used. PL spectra were measured on the oriented crystals.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09096\",\n        \"dataset_ID\": 1045,\n        \"id\": 262,\n        \"compound_name\": \"Guanidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C(NH2)3)(CH3NH3)3Pb3I10\",\n        \"group\": \"(Gua)(MA)3Pb3I10, (GA)(MA)3Pb3I10, diaminomethanaminium tris(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"CH6N3, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"diaminomethanaminium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"New Type of 2D Perovskites with Alternating Cations in the Interlayer Space, (C(NH2)3)(CH3NH3)nPbnI3n+1: Structure, Properties, and Photovoltaic Performance\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16297\",\n        \"pages_end\": \"16309\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead oxide (PbO, 99%), methylamine hydrochloride (CH3NH3Cl, 99%), guanidine hydrochloride (C(NH2)3Cl, \\u226598%), hydriodic acid (HI, 57 wt % in H2O), hypophosphorous acid (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"Black single crystals\",\n        \"synthesis_description\": \"PbO (2232 mg, 10 mmol) was dissolved with 20.0 mL HI and 1.7 mL H3PO2 and heated to boiling under constant stirring for over 15 minutes. Then CH3NH3Cl (675 mg, 10 mmol) and C(NH2)3Cl (318 mg, 3.33 mmol), were added and continued to be reflexed/stirred until the reactants dissolved. Then stirring was stopped and the solution was gradually cooled to room temperature, causing black crystals to precipitate. The crystals were allowed to stand for two hours and were then removed by suction filtration and dried at 60 degrees Celsius in a vacuum oven.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer was used for diffuse reflectance spectroscopy of the powdered samples at room temperature. BASO4 was used as the 100% reflectance reference, and the Kubelka-Munk transofmraiton was used to convert the data to absorbance. The band gap value was estimated by extrapolating the absorbance data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1046,\n        \"id\": 263,\n        \"compound_name\": \"Histammonium lead iodide\",\n        \"formula\": \"(C5H11N3)PbI4\",\n        \"group\": \"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Dark orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1047,\n        \"id\": 263,\n        \"compound_name\": \"Histammonium lead iodide\",\n        \"formula\": \"(C5H11N3)PbI4\",\n        \"group\": \"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Dark orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Time-Resolved Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1048,\n        \"id\": 263,\n        \"compound_name\": \"Histammonium lead iodide\",\n        \"formula\": \"(C5H11N3)PbI4\",\n        \"group\": \"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Dark orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1049,\n        \"id\": 263,\n        \"compound_name\": \"Histammonium lead iodide\",\n        \"formula\": \"(C5H11N3)PbI4\",\n        \"group\": \"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Dark orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1050,\n        \"id\": 264,\n        \"compound_name\": \"Histammonium tin iodide\",\n        \"formula\": \"(C5H11N3)SnI4\",\n        \"group\": \"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Black plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1051,\n        \"id\": 264,\n        \"compound_name\": \"Histammonium tin iodide\",\n        \"formula\": \"(C5H11N3)SnI4\",\n        \"group\": \"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Black plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Time-Resolved Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1052,\n        \"id\": 264,\n        \"compound_name\": \"Histammonium tin iodide\",\n        \"formula\": \"(C5H11N3)SnI4\",\n        \"group\": \"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1053\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Black plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1053,\n        \"id\": 264,\n        \"compound_name\": \"Histammonium tin iodide\",\n        \"formula\": \"(C5H11N3)SnI4\",\n        \"group\": \"(HIS)SnI4, (HA)SnI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodostannate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1052\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, histamine dihydrochloride\",\n        \"synthesis_product\": \"Black plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Histamine dihydrochloride was then dissolved into another HI solution and also heated (1:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1054,\n        \"id\": 217,\n        \"compound_name\": \"Bis(benzylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"bis(benzylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1055,\n        \"id\": 217,\n        \"compound_name\": \"Bis(benzylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"bis(benzylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Time-Resolved Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1056,\n        \"id\": 217,\n        \"compound_name\": \"Bis(benzylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"bis(benzylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1057\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1057,\n        \"id\": 217,\n        \"compound_name\": \"Bis(benzylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"(BZA)2PbI4, Benzylammonium lead iodide, (C6H5CH2NH3)2PbI4, bis(benzylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"bis(benzylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1056\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to PbO). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1058,\n        \"id\": 265,\n        \"compound_name\": \"Bis(benzylammonium) tin iodide\",\n        \"formula\": \"(C7NH10)2SnI4\",\n        \"group\": \"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(benzylaminium) tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Either a STOE IPDS 2 or IPDS 2T diffractometer with Mo Kalpha radiation operated at 50 kV and 40 mA in a nitrogen atmosphere was used. Integration and absorption corrections were made with the STOE X-AREA programs. Structure was solved directly and refined with full-matrix least-squares on F2 with the OLEX2 program package.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1059,\n        \"id\": 265,\n        \"compound_name\": \"Bis(benzylammonium) tin iodide\",\n        \"formula\": \"(C7NH10)2SnI4\",\n        \"group\": \"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(benzylaminium) tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Time-Resolved Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"TR-PL was collected at room temperature using the Hamamatsu C4334 Steakscope streack camera system. The instrument response function is about 30 picoseconds and the temporal resolution after deconvolution fitting is about 10 picoseconds. 400 excitation pulses were generated at a high repetition rate from an ultrafast laser system.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1060,\n        \"id\": 265,\n        \"compound_name\": \"Bis(benzylammonium) tin iodide\",\n        \"formula\": \"(C7NH10)2SnI4\",\n        \"group\": \"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(benzylaminium) tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1061\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b03054\",\n        \"dataset_ID\": 1061,\n        \"id\": 265,\n        \"compound_name\": \"Bis(benzylammonium) tin iodide\",\n        \"formula\": \"(C7NH10)2SnI4\",\n        \"group\": \"(BZA)2SnI4, Benzylammonium tin iodide, bis(benzylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(benzylaminium) tin iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1060\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Role of Organic Counterion in Lead- and Tin-Based Two-Dimensional Semiconducting Iodide Perovskites and Application in Planar Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"7781\",\n        \"pages_end\": \"7792\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnCl2\\u00b72H2O, HI, H3PO2, benzylamine hydrochloride\",\n        \"synthesis_product\": \"Dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u00b72H2O was dissolved in a solution with HI and H3PO2 and heated while stirring for 20 minutes at 120 degrees Celsius. The solution became bright yellow. Benzylamine hydrochloride was then dissolved into another HI solution and also heated (2:1 molar ratio to Sn). Then the latter solution was carefully layered on top of the PbI2 solution and dark orange crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to measure optical diffuse reflectance at room temperature. BaSO4 was used as the 100% reflectance reference. Reflectance vs wavelength was used to get the absorption spectrum via the Kubelka-Munk equation, which was then used to extrapolate the optical band gaps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1062,\n        \"id\": 91,\n        \"compound_name\": \"3-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C6H16N2PbI4\",\n        \"group\": \"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1063\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1063,\n        \"id\": 91,\n        \"compound_name\": \"3-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C6H16N2PbI4\",\n        \"group\": \"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1062\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1064,\n        \"id\": 91,\n        \"compound_name\": \"3-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C6H16N2PbI4\",\n        \"group\": \"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1065\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1065,\n        \"id\": 91,\n        \"compound_name\": \"3-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C6H16N2PbI4\",\n        \"group\": \"3-(methanaminium)piperidinium tetraiodoplumbate(II), (3-AMP)PbI14, (3AMP)PbI4, (C6N2H16)PbI4\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1064\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 342 mg (3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1066,\n        \"id\": 266,\n        \"compound_name\": \"3-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Dark red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker Molly instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) with MX Optics at 250 K.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1067,\n        \"id\": 266,\n        \"compound_name\": \"3-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1068\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Dark red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1068,\n        \"id\": 266,\n        \"compound_name\": \"3-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1067\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Dark red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Spectra were recorded using HORIBA LabRAM HR Evolution confocal RAMAN microscope.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1069,\n        \"id\": 266,\n        \"compound_name\": \"3-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Dark red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1070,\n        \"id\": 266,\n        \"compound_name\": \"3-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), methylammonium iodide (MAI), PbO, HI, H3PO2\",\n        \"synthesis_product\": \"Dark red crystals\",\n        \"synthesis_description\": \"PbO powder was dissolved in a solution of HI and H3PO2 that was heated and stirred for 5-10 minutes at around 130 degrees Celsius. The solution became clear and bright yellow. Then MAI was added to the same solution while still being held at 130 degrees. HI was added to the organic cation (3AMP or 4AMP) in a separate vial under similar conditions. The molar ratio 4AMP:MAI:PbO was 0.5:2:3. The latter solution was then added to the former solution and heated/stirred at 240 degrees for 5 minutes. Slow cooling afterwards to room temperature caused crystals to precipitate.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The band gaps of the systems were extrapolated after converting reflectance to absorption via the Kubelka-Munk relation.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1071,\n        \"id\": 267,\n        \"compound_name\": \"3-(aminomethyl)piperidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker Molly instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) with MX Optics at 250 K.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pa\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1072,\n        \"id\": 267,\n        \"compound_name\": \"3-(aminomethyl)piperidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1073\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pa\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1073,\n        \"id\": 267,\n        \"compound_name\": \"3-(aminomethyl)piperidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1072\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pa\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1074,\n        \"id\": 267,\n        \"compound_name\": \"3-(aminomethyl)piperidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1075\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pa\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1075,\n        \"id\": 267,\n        \"compound_name\": \"3-(aminomethyl)piperidinium bis(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(3-AMP)(MA)2Pb3I10, (3AMP)(MA)2Pb3I10, 3-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1074\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 477 mg (3 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 37.6 mg (0.33 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pa\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1076,\n        \"id\": 268,\n        \"compound_name\": \"3-(aminomethyl)piperidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using either an STOE IPDS 2 or an IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1077,\n        \"id\": 268,\n        \"compound_name\": \"3-(aminomethyl)piperidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1078\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1078,\n        \"id\": 268,\n        \"compound_name\": \"3-(aminomethyl)piperidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1077\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1079,\n        \"id\": 268,\n        \"compound_name\": \"3-(aminomethyl)piperidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1080\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1080,\n        \"id\": 268,\n        \"compound_name\": \"3-(aminomethyl)piperidinium tris(methylammonium) lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(3-AMP)(MA)3Pb4I13, (3AMP)(MA)3Pb4I13, 3-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-05-15\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1079\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"892 mg (4 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 636 mg (4 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 34.2 mg (0.3 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1081,\n        \"id\": 269,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"(C6H16N2)PbI4\",\n        \"group\": \"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using either an STOE IPDS 2 or an IPDS 2T diffractometer with graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) (50 kV/40 mA) under N2.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1082,\n        \"id\": 269,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"(C6H16N2)PbI4\",\n        \"group\": \"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1083\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1083,\n        \"id\": 269,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"(C6H16N2)PbI4\",\n        \"group\": \"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1082\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1084,\n        \"id\": 269,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"(C6H16N2)PbI4\",\n        \"group\": \"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1085\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1085,\n        \"id\": 269,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"(C6H16N2)PbI4\",\n        \"group\": \"(4-AMP)PbI4, (4AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1084\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. In a separate vial, 0.5 mL HI was added to 3 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating at 240 \\u00b0C and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1086,\n        \"id\": 270,\n        \"compound_name\": \"4-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker Molly instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) with MX Optics at 250 K.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1087,\n        \"id\": 270,\n        \"compound_name\": \"4-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1088\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1088,\n        \"id\": 270,\n        \"compound_name\": \"4-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1087\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1089,\n        \"id\": 270,\n        \"compound_name\": \"4-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1090\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1090,\n        \"id\": 270,\n        \"compound_name\": \"4-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(4-AMP)(MA)Pb2I7, (4AMP)(MA)Pb2I7, 4-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1089\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.5 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1091,\n        \"id\": 271,\n        \"compound_name\": \"4-(aminomethyl)piperidinium bis(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker Molly instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) with MX Optics at 250 K.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1092,\n        \"id\": 271,\n        \"compound_name\": \"4-(aminomethyl)piperidinium bis(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1093\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1093,\n        \"id\": 271,\n        \"compound_name\": \"4-(aminomethyl)piperidinium bis(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1092\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1094,\n        \"id\": 271,\n        \"compound_name\": \"4-(aminomethyl)piperidinium bis(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1095\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1095,\n        \"id\": 271,\n        \"compound_name\": \"4-(aminomethyl)piperidinium bis(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)2Pb3I10\",\n        \"group\": \"(4-AMP)(MA)2Pb3I10, (4AMP)(MA)2Pb3I10, 4-(methanaminium)piperidinium bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium bis(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1094\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 3 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.33 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1096,\n        \"id\": 272,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tris(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected using a Bruker Molly instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) with MX Optics at 250 K.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1097,\n        \"id\": 272,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tris(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1098\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1098,\n        \"id\": 272,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tris(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1097\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A HORIBA LabRAM HR Evolution confocal RAMAN microscope was used to collect the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1099,\n        \"id\": 272,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tris(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1100\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 1100,\n        \"id\": 272,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tris(methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)3Pb4I13\",\n        \"group\": \"(4-AMP)(MA)3Pb4I13, (4AMP)(MA)3Pb4I13, 4-(methanaminium)piperidinium tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tris(methanaminium) lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1099\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (4AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"4 mmol PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 4 mmol MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 0.27 mmol 4AMP under stirring. The protonated 4AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1102,\n        \"id\": 274,\n        \"compound_name\": \"Guanidinium caesium lead iodide\",\n        \"formula\": \"(C(NH2)3)CsPbI4\",\n        \"group\": \"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbI4, Caesium lead iodide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Smart Platform diffractometer using an Apex I CCD detector and Mo Kalpha radiation was used for SCXRD. APEX3 software processed the data and the SHELXT and SHELXL programs within the Olex2 package were used to solve and refine the structure.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnnm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1103,\n        \"id\": 274,\n        \"compound_name\": \"Guanidinium caesium lead iodide\",\n        \"formula\": \"(C(NH2)3)CsPbI4\",\n        \"group\": \"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbI4, Caesium lead iodide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calculated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1104,\n        \"id\": 274,\n        \"compound_name\": \"Guanidinium caesium lead iodide\",\n        \"formula\": \"(C(NH2)3)CsPbI4\",\n        \"group\": \"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbI4, Caesium lead iodide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calculated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1105,\n        \"id\": 274,\n        \"compound_name\": \"Guanidinium caesium lead iodide\",\n        \"formula\": \"(C(NH2)3)CsPbI4\",\n        \"group\": \"(Gua)CsPbI4, (GA)CsPbI4, diaminomethanaminium caesium tetraiodoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbI4, Caesium lead iodide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), Cesium iodide (CsI, 99.9%), Lead(II) iodide (PbI2, 99%), hydriodic acid (HI, 57%, stabilized with 1.5% hypophosphorous acid, H3PO2)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"CsI (1.55 mmol), [C(NH2)3]2Co3 (6 mmol), PbI2 (1.55 mmol), and 10 mL of HI were combined, and immediately a red solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing red crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Joule-Thomson cryostat from MMR Technologies was used to control the temperature in the range of 78 to 300 K. The samples were heated at about 5 K per minute. A 355 nm Nd:YAG laser and a 405 nm CW diode laser were used. An SP-2300 spectrograph from Princeton Instruments was used to record the PL emission that was collimated with an optical fiber. It was also coupled with a CCD array and the spectra were calibrated by using Planck irradiation from a calibrated halogen lamp as reference.\",\n        \"physical_property\": \"77.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1106,\n        \"id\": 275,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)CsPbBr4\",\n        \"group\": \"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbBr4, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Smart Platform diffractometer using an Apex I CCD detector and Mo Kalpha radiation was used for SCXRD. APEX3 software processed the data and the SHELXT and SHELXL programs within the Olex2 package were used to solve and refine the structure.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1108,\n        \"id\": 275,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)CsPbBr4\",\n        \"group\": \"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbBr4, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Absorption Spectra\",\n        \"experimental_description\": \"A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1109,\n        \"id\": 275,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)CsPbBr4\",\n        \"group\": \"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbBr4, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Joule-Thomson cryostat from MMR Technologies was used to control the temperature in the range of 78 to 300 K. The samples were heated at about 5 K per minute. A 355 nm Nd:YAG laser and a 405 nm CW diode laser were used. An SP-2300 spectrograph from Princeton Instruments was used to record the PL emission that was collimated with an optical fiber. It was also coupled with a CCD array and the spectra were calibrated by using Planck irradiation from a calibrated halogen lamp as reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1111,\n        \"id\": 276,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)Cs2Pb2Br7\",\n        \"group\": \"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Cs2Pb2Br7, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead bromide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow needle-like crystals\",\n        \"synthesis_description\": \"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Smart Platform diffractometer using an Apex I CCD detector and Mo Kalpha radiation was used for SCXRD. APEX3 software processed the data and the SHELXT and SHELXL programs within the Olex2 package were used to solve and refine the structure.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmmm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1113,\n        \"id\": 276,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)Cs2Pb2Br7\",\n        \"group\": \"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Cs2Pb2Br7, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead bromide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, integrating sphere)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow needle-like crystals\",\n        \"synthesis_description\": \"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1114,\n        \"id\": 276,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)Cs2Pb2Br7\",\n        \"group\": \"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Cs2Pb2Br7, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead bromide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow needle-like crystals\",\n        \"synthesis_description\": \"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1115,\n        \"id\": 275,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)CsPbBr4\",\n        \"group\": \"(Gua)CsPbBr4, (GA)CsPbBr4, diaminomethanaminium caesium tetrabromoplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"CsPbBr4, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead (II) bromide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"CsBr (2 mmol), [C(NH2)3]2Co3 (6 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Absorption Spectra\",\n        \"experimental_description\": \"A Jasco V670 spectrophotometer with deuterium and halogen lamps and an integrating sphere was used to record the UV-vis absorbance spectra. It was estimated from the reflectance and transmittance spectra collected from a thin powder layer of the compound. Absorbance was calclulated from the Kubelka-Munk equation. Band gaps were also extrapolated from the absorbance spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01204\",\n        \"dataset_ID\": 1116,\n        \"id\": 276,\n        \"compound_name\": \"Guanidinium caesium lead bromide\",\n        \"formula\": \"(C(NH2)3)Cs2Pb2Br7\",\n        \"group\": \"(Gua)Cs2Pb2Br7, (GA)Cs2Pb2Br7, diaminomethanaminium dicaesium septabromo diplumbate(II)\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Cs2Pb2Br7, Caesium lead bromide\",\n        \"iupac\": \"diaminomethanaminium caesium lead bromide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent and Photoconductive Layered Lead Halide Perovskite Compounds Comprising Mixtures of Cesium and Guanidinium Cations\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"11552\",\n        \"pages_end\": \"11564\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"guanidinium carbonate ([C(NH2)3]2CO3, 99+%), cesium bromide (CsBr, 99.9%), Lead(II) bromide (PbBr2, 98+%), hydrobromic acid (HBr, 48% water solution)\",\n        \"synthesis_product\": \"Yellow needle-like crystals\",\n        \"synthesis_description\": \"CsBr (1 mmol), [C(NH2)3]2Co3 (3 mmol), PbBr2 (2 mmol), and 12 mL of HBr were combined, and immediately a yellow solid precipitated. It was dissolved by heating and the solution became clear and yellow. The solution was then cooled to room temperature, causing yellow crystals to precipitate. Vacuum filtration was used to remove the crystals. They were then cleaned with diethyl ether and vacuum dried at 60 degrees Celsius.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Joule-Thomson cryostat from MMR Technologies was used to control the temperature in the range of 78 to 300 K. The samples were heated at about 5 K per minute. A 355 nm Nd:YAG laser and a 405 nm CW diode laser were used. An SP-2300 spectrograph from Princeton Instruments was used to record the PL emission that was collimated with an optical fiber. It was also coupled with a CCD array and the spectra were calibrated by using Planck irradiation from a calibrated halogen lamp as reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.chempr.2017.02.004\",\n        \"dataset_ID\": 1117,\n        \"id\": 278,\n        \"compound_name\": \"Bis(butylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"group\": \"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"High Members of the 2D Ruddlesden-Popper Halide Perovskites: Synthesis, Optical Properties, and Solar Cells of (CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"journal\": \"Chem\",\n        \"vol\": \"2\",\n        \"pages_start\": \"427\",\n        \"pages_end\": \"440\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO, MACL, n-butylamine, HI, H3PO2\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL,\\r\\n31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"An image plate STOE IPDS II diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) operated at 50 kV and 40 mA was used for SCXRD. The X-AREA suite was used for data reduction and absorption corrections. Charge flipping was used to solve the structure and refinement was performed by full-matrix least squares on F2 using the Jana2006 package.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Acam\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.chempr.2017.02.004\",\n        \"dataset_ID\": 1118,\n        \"id\": 278,\n        \"compound_name\": \"Bis(butylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"group\": \"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"High Members of the 2D Ruddlesden-Popper Halide Perovskites: Synthesis, Optical Properties, and Solar Cells of (CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"journal\": \"Chem\",\n        \"vol\": \"2\",\n        \"pages_start\": \"427\",\n        \"pages_end\": \"440\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO, MACL, n-butylamine, HI, H3PO2\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double beam, double-monochromator spectrophotometer was used to measure the optical diffuse reflectance spectra of powdered samples. BaSO4 was used as the 100% reflectance reference. The band gap was estimated after correcting for the excitonic peak and the Urbach tail in the absorption spectrum.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.chempr.2017.02.004\",\n        \"dataset_ID\": 1119,\n        \"id\": 278,\n        \"compound_name\": \"Bis(butylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"group\": \"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"High Members of the 2D Ruddlesden-Popper Halide Perovskites: Synthesis, Optical Properties, and Solar Cells of (CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"journal\": \"Chem\",\n        \"vol\": \"2\",\n        \"pages_start\": \"427\",\n        \"pages_end\": \"440\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO, MACL, n-butylamine, HI, H3PO2\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double beam, double-monochromator spectrophotometer was used to measure the optical diffuse reflectance spectra of powdered samples. BaSO4 was used as the 100% reflectance reference. The band gap was estimated after correcting for the excitonic peak and the Urbach tail in the absorption spectrum.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.chempr.2017.02.004\",\n        \"dataset_ID\": 1120,\n        \"id\": 278,\n        \"compound_name\": \"Bis(butylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"group\": \"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"High Members of the 2D Ruddlesden-Popper Halide Perovskites: Synthesis, Optical Properties, and Solar Cells of (CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"journal\": \"Chem\",\n        \"vol\": \"2\",\n        \"pages_start\": \"427\",\n        \"pages_end\": \"440\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO, MACL, n-butylamine, HI, H3PO2\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer was used to measure PL spectra on the crystals. A diode continuous wave laser, exciting at 473 nm, and a Synapse charge-coupled device camera was part of the instrument. The laser beam was parallel to the (010) direction of the crystals and was aimed at an area of 10 square microns on the surface.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.chempr.2017.02.004\",\n        \"dataset_ID\": 1121,\n        \"id\": 278,\n        \"compound_name\": \"Bis(butylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"group\": \"(BA)2(MA)4Pb5I16, bis(butane-1-aminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-06-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"High Members of the 2D Ruddlesden-Popper Halide Perovskites: Synthesis, Optical Properties, and Solar Cells of (CH3(CH2)3NH3)2(CH3NH3)4Pb5I16\",\n        \"journal\": \"Chem\",\n        \"vol\": \"2\",\n        \"pages_start\": \"427\",\n        \"pages_end\": \"440\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbO, MACL, n-butylamine, HI, H3PO2\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"PbO (4,464 mg, 20 mmol) was dissolved in a solution of HI (20.0 mL, 152 mmol) and H3PO2 (3.4 mL, 31 mmol) and heated to boiling while being stirred for ~20 minutes, until a yellow solution formed. Then (MA)Cl (1,080 mg, 16 mmol) was added and immediately caused black powder to precipitate, which was re-dissolved from stirring and the solution became clear and bright-yellow again. Separately, n-butylamine (396 mL, 4 mmol) was added to HI (10 mL, 76 mmol) in an ice bath, making a pale-yellow solution. The solution was added to the former, and again a black solid immediately precipitated. It was dissolved by heating to boiling, at which point stirring ceased. Then the solution slowly cooled to room temperature and black solids began to crystalize. The solution was left for a day and then the crystals were removed by suction filtration. Lastly, they were dried at 60 degrees in a vacuum oven overnight.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer was used to measure PL spectra on the crystals. A diode continuous wave laser, exciting at 473 nm, and a Synapse charge-coupled device camera was part of the instrument. The laser beam was parallel to the (010) direction of the crystals and was aimed at an area of 10 square microns on the surface.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.7b02322\",\n        \"dataset_ID\": 1122,\n        \"id\": 242,\n        \"compound_name\": \"bis(methylammonium) potassium yttrium chloride\",\n        \"formula\": \"C2H12N2KYCl6\",\n        \"group\": \"(MA)2KYCl6, (CH3NH3)2KYCl6, bis(methanaminium) trichloropotassiate(I) trichloroyttriate(III)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"KYCl6, Potassium chloride yttrium\",\n        \"iupac\": \"bis(methanaminium) potassium yttrium chloride\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Characterization of the Rare-Earth Hybrid Double Perovskites: (CH3NH3)2KGdCl6 and (CH3NH3)2KYCl6\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"8\",\n        \"pages_start\": \"5015\",\n        \"pages_end\": \"5020\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Y2O3, KCl, (MA)Cl, HCl\",\n        \"synthesis_product\": \"Colorless single crystals\",\n        \"synthesis_description\": \"Y2O3 or Gd2O3, KCL, and (MA)Cl were dissolved in an HCl solution inside a capped glass vial. It was held at 80 degrees Celsius and stirred for one hour, becoming clear and colorless. The cap was opened, and the solution was evaporated at 85 degrees leaving behind crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an Xcalibur/Gemini Ultra diffractometer and an Eos CCD area detector.\",\n        \"physical_property\": \"300.0 (\\u00b10.14)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3m\",\n        \"extraction_method\": \"Extracted from a publication and corresponding CCDC database files.\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b07776\",\n        \"dataset_ID\": 1129,\n        \"id\": 280,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C12H32I8N4Pb2\",\n        \"group\": \"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ferroelectricity and Rashba Effect in a Two-Dimensional Dion-Jacobson Hybrid Organic\\u2013Inorganic Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15972\",\n        \"pages_end\": \"15976\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",\n        \"synthesis_product\": \"orange single-crystals\",\n        \"synthesis_description\": \"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110\\u00ba C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker AXS D8 Venture Single Crystal X-ray Diffractometer with a Photon 100 CMOS active pixel sensor detector as well as a four-circle goniometer with Kappa geometry was used for SC-XRD. Software package APEX3 was used for data collection, reduction, and absorption correction. Structures were determined with the SHELXTL package.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b07776\",\n        \"dataset_ID\": 1130,\n        \"id\": 280,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C12H32I8N4Pb2\",\n        \"group\": \"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ferroelectricity and Rashba Effect in a Two-Dimensional Dion-Jacobson Hybrid Organic\\u2013Inorganic Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15972\",\n        \"pages_end\": \"15976\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",\n        \"synthesis_product\": \"orange single-crystals\",\n        \"synthesis_description\": \"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110\\u00ba C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker AXS D8 Venture Single Crystal X-ray Diffractometer with a Photon 100 CMOS active pixel sensor detector as well as a four-circle goniometer with Kappa geometry was used for SC-XRD. Software package APEX3 was used for data collection, reduction, and absorption correction. Structures were determined with the SHELXTL package.\",\n        \"physical_property\": \"373.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b07776\",\n        \"dataset_ID\": 1131,\n        \"id\": 280,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C12H32I8N4Pb2\",\n        \"group\": \"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1133\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ferroelectricity and Rashba Effect in a Two-Dimensional Dion-Jacobson Hybrid Organic\\u2013Inorganic Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15972\",\n        \"pages_end\": \"15976\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",\n        \"synthesis_product\": \"orange single-crystals\",\n        \"synthesis_description\": \"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110\\u00ba C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using a Horiba Fluorolog.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b07776\",\n        \"dataset_ID\": 1132,\n        \"id\": 280,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C12H32I8N4Pb2\",\n        \"group\": \"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1135\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ferroelectricity and Rashba Effect in a Two-Dimensional Dion-Jacobson Hybrid Organic\\u2013Inorganic Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15972\",\n        \"pages_end\": \"15976\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",\n        \"synthesis_product\": \"orange single-crystals\",\n        \"synthesis_description\": \"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110\\u00ba C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Solid state diffuse reflectance UV-vis spectra were measured via a UV-2450-Shimadzu UV-visible spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b07776\",\n        \"dataset_ID\": 1133,\n        \"id\": 280,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C12H32I8N4Pb2\",\n        \"group\": \"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1131\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ferroelectricity and Rashba Effect in a Two-Dimensional Dion-Jacobson Hybrid Organic\\u2013Inorganic Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15972\",\n        \"pages_end\": \"15976\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",\n        \"synthesis_product\": \"orange single-crystals\",\n        \"synthesis_description\": \"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110\\u00ba C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using a Horiba Fluorolog.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b07776\",\n        \"dataset_ID\": 1134,\n        \"id\": 280,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C12H32I8N4Pb2\",\n        \"group\": \"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ferroelectricity and Rashba Effect in a Two-Dimensional Dion-Jacobson Hybrid Organic\\u2013Inorganic Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15972\",\n        \"pages_end\": \"15976\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",\n        \"synthesis_product\": \"orange single-crystals\",\n        \"synthesis_description\": \"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110\\u00ba C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using a Horiba Fluorolog.\",\n        \"physical_property\": \"373.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b07776\",\n        \"dataset_ID\": 1135,\n        \"id\": 280,\n        \"compound_name\": \"4-(aminomethyl)piperidinium lead iodide\",\n        \"formula\": \"C12H32I8N4Pb2\",\n        \"group\": \"DJP, (AMP)PbI4, 4-(methanaminium)piperidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1132\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ferroelectricity and Rashba Effect in a Two-Dimensional Dion-Jacobson Hybrid Organic\\u2013Inorganic Perovskite\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"15972\",\n        \"pages_end\": \"15976\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"4-(aminomethyl)piperidine (AMP), HI (57 wt.% in water), PbO, H3PO2 (50 wt.%)\",\n        \"synthesis_product\": \"orange single-crystals\",\n        \"synthesis_description\": \"AMPI2 was first prepared by reacting AMP with HI. Next, AMPI2 (185.0 mg, 0.500 mmol) and PbO (111.6 mg, 0.500 mmol) were dissolved in concentrated 4 mL HI. 0.5 mL H3PO2 was added and the vial was sealed and kept at 110\\u00ba C for 1 hour. Over a time span of 30 hours, the vial cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Solid state diffuse reflectance UV-vis spectra were measured via a UV-2450-Shimadzu UV-visible spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1136,\n        \"id\": 283,\n        \"compound_name\": \"4-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was being heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr..\",\n        \"experimental_method\": \"Single crystal X-ray diffraction (XRD)\",\n        \"experimental_description\": \"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1137,\n        \"id\": 481,\n        \"compound_name\": \"3-aminomethylpyridinium 4-aminomethylpyridinium tin iodide\",\n        \"formula\": \"(3AMPY)0.5(4AMPY)0.5Sn2I6\",\n        \"group\": \"*\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"piperidin-3-ylmethanaminium piperidin-4-ylmethanaminium tin iodide\",\n        \"last_update\": \"2022-06-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (3AMPY, 99%), and 4-(aminomethyl)pyridine (4AMPY, 98%)\",\n        \"synthesis_product\": \"dark red cube shaped crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol, 451.3 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3AMPY and 4AMPY (0.5 mmol, 50.8 \\u03bcL) were added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240\\u00ba C and stirred for 5 minutes. Then, the temperature was lowered to 125 \\u00ba C until red crystals formed.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction (XRD)\",\n        \"experimental_description\": \"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1138,\n        \"id\": 282,\n        \"compound_name\": \"3-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2022-06-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240\\u00ba C and stirred for 5 minutes. Then, the temperature was lowered to 125 \\u00ba C until red crystals formed. After 1 hour, most crystals had formed, the product was obtained by suction filtration from hot solution, and finally fried for 30 more minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using Tauc plot with indirect band gap approximation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1139,\n        \"id\": 282,\n        \"compound_name\": \"3-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2022-06-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Raman Shift\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240\\u00ba C and stirred for 5 minutes. Then, the temperature was lowered to 125 \\u00ba C until red crystals formed. After 1 hour, most crystals had formed, the product was obtained by suction filtration from hot solution, and finally fried for 30 more minutes.\",\n        \"experimental_method\": \"Raman spectroscopy\",\n        \"experimental_description\": \"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1140,\n        \"id\": 282,\n        \"compound_name\": \"3-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2022-06-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution, while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240\\u00ba C and stirred for 5 minutes. Then, the temperature was lowered to 125 \\u00ba C until red crystals formed. After 1 hour, most crystals had formed, the product was obtained by suction filtration from hot solution, and finally fried for 30 more minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to obtain optical diffuse reflectance measurements. The reflectance v. wavelength data was converted to absorption v. wavelength using the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, \\u03b1 = absorption, and S = scattering coefficients.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1141,\n        \"id\": 282,\n        \"compound_name\": \"3-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2022-06-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O),  3-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO (2 mmol, 446.4 mg) was dissolved in 2.5 mL of HI solution while being heated and stirred. Once a yellow solution appeared, 3-(aminomethyl)pyridine (3AMPY) (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined at 240\\u00ba C and stirred for 5 minutes. Then, the temperature was lowered to 125 \\u00ba C until red crystals formed.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1142,\n        \"id\": 283,\n        \"compound_name\": \"4-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was heated and stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using Tauc plot with indirect band gap approximation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1143,\n        \"id\": 283,\n        \"compound_name\": \"4-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Raman Shift\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was heated and stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr.\",\n        \"experimental_method\": \"Raman spectroscopy\",\n        \"experimental_description\": \"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1144,\n        \"id\": 283,\n        \"compound_name\": \"4-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"2 mmol of PbO was dissolved in 2.5 mL of HI, and the solution was heated and stirred. Once a yellow solution was obtained, 4AMPY (0.4 mmol, 40.6 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration after ~1 hr.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to obtain optical diffuse reflectance measurements. The reflectance v. wavelength data was converted to absorption v. wavelength using the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, \\u03b1 = absorption, and S = scattering coefficients.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Engauge Digitizer Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1145,\n        \"id\": 483,\n        \"compound_name\": \"3-aminomethylpyridinium lead tin iodide\",\n        \"formula\": \"(3AMPY)(Pb1\\u2013xSnx)2I6 with x = 0.25\",\n        \"group\": \"(3AMPY)(Sn/Pb)2I6\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb0.75Sn0.25\",\n        \"iupac\": \"piperidin-3-ylmethanaminium lead (II) tin (II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\n        \"synthesis_product\": \"black, plated crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (1.5 mmol) and 0.5 mmol PbO were dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1146,\n        \"id\": 284,\n        \"compound_name\": \"3-aminomethylpyridinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\n        \"synthesis_product\": \"black, plated crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was being heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. Temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration and most product was formed within 1 hour.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using the Tauc plot with an indirect band gap approximation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1147,\n        \"id\": 284,\n        \"compound_name\": \"3-aminomethylpyridinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Raman Shift\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\n        \"synthesis_product\": \"black, plated crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"Raman spectroscopy\",\n        \"experimental_description\": \"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Engauge Digitizer Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1148,\n        \"id\": 284,\n        \"compound_name\": \"3-aminomethylpyridinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%)\",\n        \"synthesis_product\": \"black, plated crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used to obtain optical diffuse reflectance measurements. The reflectance v. wavelength data was converted to absorption v. wavelength using the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, \\u03b1 = absorption, and S = scattering coefficients.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1149,\n        \"id\": 286,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)-pyridine (98%)\",\n        \"synthesis_product\": \"dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1150,\n        \"id\": 285,\n        \"compound_name\": \"(3AMPY)0.5(4AMPY)0.5Sn2I6\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"3-(methanaminium)pyridinium 4-(methanaminium)pyridinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium 4-(methanaminium)pyridinium tin iodide\",\n        \"last_update\": \"2022-07-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%), and 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.25 mmol, 50.8 \\u03bcL) and 4AMPY (0.25 mmol) were added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using the Tauc plot with an indirect band gap approximation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1151,\n        \"id\": 284,\n        \"compound_name\": \"3-aminomethylpyridinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%).\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1152,\n        \"id\": 286,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was utilized to measure the optical diffuse reflectance. The spectrometer operated at 200-2500 nm at room temperature, and the reference was BaSO4. The band gap was found by converting the reflectance to absorption data through the Kubelka-Munk equation and using the Tauc plot with an indirect band gap approximation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1153,\n        \"id\": 286,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Raman Shift\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"Raman spectroscopy\",\n        \"experimental_description\": \"Raman spectra were obtained with a 946 nm laser excitation, and the Raman signals were collected with a CCD camera. The spectra were acquired using a 5x objective in a parallel configuration. Rayleigh scattering was suppressed with two notch filters, and Raman scattering with frequencies as low as 10 cm^{-1} were obtained. Spectra ranged from -150 cm^{-1} to 200 cm^{-1}\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1154,\n        \"id\": 283,\n        \"compound_name\": \"4-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"dark red plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 4AMPY (0.5 mmol, 50.8 \\u03bcL) was added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until dark red crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer (used within the 200-2500 nm range at room temperature) was used to obtain optical diffuse reflectance measurements. BaSO4 was a reference. The reflectance v. wavelength data produced helped estimate bandgap of the material by converting reflectance to absorption using the Kubelka-Munk equation \\u03b1/S = (1-R)^{2}(2R)^{-1}, where R = reflectance, \\u03b1 = absorption, and S = scattering coefficients.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1158,\n        \"id\": 287,\n        \"compound_name\": \"(R/S-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH3)2SnI4\",\n        \"group\": \"(MBA)2SnI4, \\u0152\\u00b1-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"(R/S-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(R)-(+)-\\u03b1-Methylbenzylamine (R-MBA, 98%, ee 96%), (S)-(\\u2212)-\\u03b1-methylbenzylamine, (S-MBA, 98%, ee 98%), (\\u00b1)-\\u03b1-methylbenzylamine (rac-MBA, 99%), tTin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), MBA (R-, S-, or rac-; 1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S instrument using Mo Kalpha radiation was used for SCXRD at 250 K. The SHELXS program was used to directly solve the structure and the SHELXL program from the Olex2 package was used for refinement.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"(R-MBA)2SnI4 - P 2(1) 2(1) 2(1)\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1159,\n        \"id\": 287,\n        \"compound_name\": \"(R/S-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH3)2SnI4\",\n        \"group\": \"(MBA)2SnI4, \\u0152\\u00b1-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"(R/S-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(\\u00b1)-\\u03b1-methylbenzylamine (rac-MBA, 99%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N,N-anhydrous DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), rac-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Cary 5000 UV-vis-NIR spectrometer operated in the 200-800 nm wavelength range was used to collect the absorption spectra. A blank quartz substrate was the 100% transmittance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1160,\n        \"id\": 287,\n        \"compound_name\": \"(R/S-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH3)2SnI4\",\n        \"group\": \"(MBA)2SnI4, \\u0152\\u00b1-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"(R/S-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"circular dichroism (CD)\",\n        \"primary_unit\": \"mDegree\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(R)-(+)-\\u03b1-Methylbenzylamine (R-MBA, 98%, ee 96%), (S)-(\\u2212)-\\u03b1-methylbenzylamine, (S-MBA, 98%, ee 98%), (\\u00b1)-\\u03b1-methylbenzylamine (rac-MBA, 99%), tTin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N,N-anhydrous DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), MBA (R-, S-, or rac-; 1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes. Linear optical and CD measurements were made on the quartz films, and mCP-AFM measurements were made on the FTO films.\",\n        \"experimental_method\": \"Circular Dichroism (CD) Spectroscopy\",\n        \"experimental_description\": \"A Jasco J-715 spectropolarimeter was used for the CD measurements. 3-5 scans of the spectra were taken and averaged. A wavelength range of 200-600 nm was used with 0.2 nm resolution.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"(R-MBA)2SnI4\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1161,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%)\",\n        \"synthesis_product\": \"(PEA)2SnI4 crystals\",\n        \"synthesis_description\": \"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 \\u02daC under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration and were stored in an N2 glove box.\",\n        \"experimental_method\": \"UV-visible absorption\",\n        \"experimental_description\": \"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using the Kubelka-Munk transformation; (\\u03b1/S = (1 \\u2212 R)^2/2R); \\u03b1 is the absorption coefficient, S is the scattering coefficient, and R is the reflectance.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1162,\n        \"id\": 287,\n        \"compound_name\": \"(R/S-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH3)2SnI4\",\n        \"group\": \"(MBA)2SnI4, \\u0152\\u00b1-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"(R/S-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Chiral-induced spin Selectivity (CISS)\",\n        \"primary_unit\": \"nA\",\n        \"secondary_name\": \"bias\",\n        \"secondary_unit\": \"V\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(R)-(+)-\\u03b1-Methylbenzylamine (R-MBA, 98%, ee 96%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N, N-anhydrous DMF\",\n        \"synthesis_product\": \"Thin-film on FTO substrate\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), R-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes.\",\n        \"experimental_method\": \"Magnetic conductive-probe atomic force microscopy\",\n        \"experimental_description\": \"The mCP-AFM measurements were made using a Bruker Icon AFM system enclosed within an Argon glovebox. The specific tip used was the \\u201cBruker MESP-V2\\u201d, and contact mode was selected. The Co-Cr coated tips were premagnetized through exposure to a strong permanent magnet for about an hour, scanning immediately afterwards. The magnetization of the tip causes the spin-degeneracy of the carriers in the tip to be lifted, causing mostly one spin-state to be injected into the sample. While scanning, the tip was grounded, and a bias was applied to the sample in the range of -1.2 to 1.2 V. A scan rate of 0.3 Hz was used. Over 100 I-V curves were generated and averaged at different locations on the sample for the three different magnetizations (north, south, none).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Tip Up\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1163,\n        \"id\": 287,\n        \"compound_name\": \"(R/S-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH3)2SnI4\",\n        \"group\": \"(MBA)2SnI4, \\u0152\\u00b1-methylbenzylammonium tin iodide, 1-phenylethylammonium tin iodide, (R/S-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"(R/S-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Chiral-induced spin Selectivity (CISS)\",\n        \"primary_unit\": \"nA\",\n        \"secondary_name\": \"bias\",\n        \"secondary_unit\": \"V\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-\\u03b1-methylbenzylamine, (S-MBA, 98%, ee 98%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water), N, N-anhydrous DMF\",\n        \"synthesis_product\": \"Thin film on FTO substrate\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), S-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight. The crystals were dissolved in DMF at the desired concentration to be used as precursors for spin coating. A spin rate of 4000 rpm for 30 seconds was used and was followed by annealing at 100 degrees for 10 minutes.\",\n        \"experimental_method\": \"Magnetic conductive-probe atomic force microscopy\",\n        \"experimental_description\": \"The mCP-AFM measurements were made using a Bruker Icon AFM system enclosed within an Argon glovebox. The specific tip used was the \\u201cBruker MESP-V2\\u201d, and contact mode was selected. The Co-Cr coated tips were premagnetized through exposure to a strong permanent magnet for about an hour, scanning immediately afterwards. The magnetization of the tip causes the spin-degeneracy of the carriers in the tip to be lifted, causing mostly one spin-state to be injected into the sample. While scanning, the tip was grounded, and a bias was applied to the sample in the range of -1.2 to 1.2 V. A scan rate of 0.3 Hz was used. Over 100 I-V curves were generated and averaged at different locations on the sample for the three different magnetizations (north, south, none).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Tip Up\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1165,\n        \"id\": 61,\n        \"compound_name\": \"Bis(dodecylammonium) lead iodide\",\n        \"formula\": \"C24H56N2PbI4\",\n        \"group\": \"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",\n        \"organic\": \"C12H28N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(dodecyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"dodecylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (Sigma Aldrich, 99.9%), decylamine (Sigma Aldrich, 99%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%)\",\n        \"synthesis_product\": \"(DA)2PbI4 crystals\",\n        \"synthesis_description\": \"(DA)2PbI4 single crystals were synthesized by dissolving lead oxide (0.5 mmol) in  20 mL of hydriodic acid by heating to boiling under constant stirring. To it, 0.5 mmol of decylamine was added. The solution was heated and stirred until the precipitate dissolved completely. Then the solution was allowed to cool naturally to room temperature.\",\n        \"experimental_method\": \"UV-visible absorption\",\n        \"experimental_description\": \"UV-Visible absorbance data were recorded on the transmission mode in Cary Series UV-Vis Spectrophotometer (Agilent Technologies).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.chemmater.8b01200\",\n        \"dataset_ID\": 1169,\n        \"id\": 288,\n        \"compound_name\": \"4-methylpiperidinium bismuth iodide: triiodide\",\n        \"formula\": \"(C6H14N)4I3BiI6\",\n        \"group\": \"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"I3BiI6, Iodide bismuth iodide\",\n        \"iupac\": \"tetrakis(4-methylpiperidinium) iodide bismuth iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Triiodide-Induced Band-Edge Reconstruction of a Lead-Free Perovskite-Derivative Hybrid for Strong Light Absorption\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"30\",\n        \"pages_start\": \"4081\",\n        \"pages_end\": \"4088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",\n        \"synthesis_product\": \"black needle-like crystals\",\n        \"synthesis_description\": \"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days. The crystals were redissolved in an oxidized HI solution, and the solution was again allowed to be evaporated over a few days.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SCXRD data were collected using an Agilent SuperNova Dual diffractometer equipped with a graphite-monochromatized Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"290.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1170,\n        \"id\": 290,\n        \"compound_name\": \"Bis(3-propanolammonium) lead iodide\",\n        \"formula\": \"C6H20N2O2PbI4\",\n        \"group\": \"(HO(CH2)3NH3)2PbI4, bis(3-propanolaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C3H10NO\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(3-propanolaminium) lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI(47%), propanolamine (HOC3H6NH2)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"PbI2 (0.495 mmol; 0.228 gm) was dissolved in 1 mL HI solution. Then HOC3H6NH2 (1.70 mmol; 0.128 g) was added and was dissolved by refluxing the solution for one hour at 90 degrees Celsius. Red crystals were then grown by cooling the solution at 2 degrees per hour to -7 degrees.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1171,\n        \"id\": 291,\n        \"compound_name\": \"Bis(2-iodoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2PbI6\",\n        \"group\": \"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-iodoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI(47%), ethanol amine (HOC2H4NH2)\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2 (0.434 mmol; 0.2 g) was dissolved in 2 mL HI solution. Then HOC2H4NH2 (0.798 mmol; 0.036 g) was added and was dissolved by refluxing for 12 hours. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled at 2 degrees Celsius per hour to room temperature, causing yellow crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1172,\n        \"id\": 292,\n        \"compound_name\": \"Bis(3-iodopropylammonium) lead iodide\",\n        \"formula\": \"C6H18N2PbI6\",\n        \"group\": \"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",\n        \"organic\": \"C3H9NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(3-iodopropylaminium) lead (II) iodide\",\n        \"last_update\": \"2023-02-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI(47%), propanolamine (HOC3H6NH2)\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2 (0.610 mmol; 0.281 g) was dissolved in 1.5 mL HI solution. Then HOC3H6NH2 (0.945 mmol; 0.071 g) was added and was dissolved by refluxing for 2 hours at 90 degrees Celsius. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled at 2 degrees Celsius per hour to room temperature, causing yellow crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1173,\n        \"id\": 293,\n        \"compound_name\": \"Bis(4-iodobutylammonium) lead iodide\",\n        \"formula\": \"C8H22N2PbI6\",\n        \"group\": \"(I(CH2)4NH3)2PbI4, bis(4-iodobutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C4H11NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(4-iodobutylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI(47%), butanolamine (HOC4H8NH2), ethyl acetate\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2 (0.178 mmol; 0.082 g) was dissolved in 1 mL HI solution. Then HOC4H8NH2 (0.449 mmol; 0.040 g) was added. The precipitate was dissolved at 3 mL ethyl acetate and was kept undisturbed at room temperature. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1174,\n        \"id\": 294,\n        \"compound_name\": \"Bis(5-iodopentylammonium) lead iodide\",\n        \"formula\": \"C10H26N2PbI6\",\n        \"group\": \"(I(CH2)5NH3)2PbI4, bis(5-iodopentylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5H13NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-iodopentylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI(47%), pentanolamine (HOC5H10NH2)\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"PbI2 (0.325 mmol; 0.236 g) was dissolved in 2 mL HI solution. Then HOC5H10NH2 (1.26 mmol; 0.130 g) was added. The precipitate was dissolved at room temperature via ultrasound. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled in a fridge to 5 degrees Celsius, causing orange crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1175,\n        \"id\": 295,\n        \"compound_name\": \"Bis(6-iodohexylammonium) lead iodide\",\n        \"formula\": \"C12H30N2PbI6\",\n        \"group\": \"(I(CH2)6NH3)2PbI4, bis(6-iodohexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H15NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(6-iodohexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI (47%), hexanolamine (HOC6H12NH2)\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"PbI2 (0.434 mmol; 0.200 g) was dissolved in 2 mL HI solution. Then HOC6H12NH2 (0.922 mmol; 0.108 g) was added. The precipitate was dissolved at room temperature via ultrasound. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom. The solution was then cooled in a fridge to 5 degrees Celsius, causing orange crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1176,\n        \"id\": 296,\n        \"compound_name\": \"Bis(2-bromoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2Br2PbI4\",\n        \"group\": \"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NBr\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-bromoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI, BrC2H4NH2\\u00b7HBr\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"PbI2 (0.113 mmol; 0.052 g)  was dissolved in 2 mL HI solution. Then BrC2H4NH2\\u00b7HBr (0.376 mmol; 0.077 g) was added. The precipitate was dissolved at room temperature via ultrasound. The solution was then cooled in a fridge to 5 degrees Celsius, causing red crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1177,\n        \"id\": 297,\n        \"compound_name\": \"2,2\\u2032-dithiodiethanammonium lead iodide\",\n        \"formula\": \"C4H14N2S2PbI4\",\n        \"group\": \"(NH3(CH2)2S-S(CH2)2NH3)PbI4, 2,2\\u201a\\u00c4\\u2264-dithiodiethanaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NS\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2,2\\u2032-dithiodiethanaminium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI (47%), HSC2H4NH2\\u00b7HCl\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"PbI2 (0.252 mmol; 0.116 g) was dissolved in 4 mL HI solution. Then HSC2H4NH2\\u00b7HCl (0.880 mmol; 0.1 g) was added and immediately formed a yellow solid. The solution was then heated 90 degrees Celsius, causing the solution to become clear after a few minutes. The solution was then cooled to room temperature at the rate of 2 degrees per hour, causing yellow and orange crystals to precipitate. The orange crystals were the perovskite compound and the yellow crystals were (NH3(CH2)2S-S(CH2)2NH3)2PbI5\\u00b7I.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 1178,\n        \"id\": 298,\n        \"compound_name\": \"Iodo-bis(2,2\\u2032-dithiodiethanammonium) lead iodide\",\n        \"formula\": \"C8H28N4S4PbI6\",\n        \"group\": \"(NH3(CH2)2S-S(CH2)2NH3)2PbI5\\u00ac\\u2211I, iodo-bis(2,2\\u201a\\u00c4\\u2264-dithiodiethanaminium) pentaiodoplumbate(II)\",\n        \"organic\": \"C4H14N2S2I\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"iodo-bis(2,2\\u2032-dithiodiethanaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI (47%), HSC2H4NH2\\u00b7HCl\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2 (0.252 mmol; 0.116 g) was dissolved in 4 mL HI solution. Then HSC2H4NH2\\u00b7HCl (0.880 mmol; 0.1 g) was added and immediately formed a yellow solid. The solution was then heated 90 degrees Celsius, causing the solution to become clear after a few minutes. The solution was then cooled to room temperature at the rate of 2 degrees per hour, causing yellow and orange crystals to precipitate. The yellow crystals were used for the experiment.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to measure SCXRD at 173 K. Omega-scans of width 0.3 degrees were used. The SAINT+ version 6.02 program was used for data reduction and the XPREP program was used for absorption corrections. SHELXS-97 was used to directly solve the structure. SHELXL-97 was used for refinement of the structure.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1179,\n        \"id\": 299,\n        \"compound_name\": \"Bis(naphthaleneoxyethylammonium) lead iodide\",\n        \"formula\": \"(C12H14ON)2PbI4, C24H28O2N2PbI4\",\n        \"group\": \"(Nap-O-Et-NH3)2PbI4, (naphthalene-O-ethyl-NH3)2PbI4, bis(naphthaleneoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C12H14ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Dichloromethane, \\u03b3-butyrolactone (GBL), naphthaleneoxyethylammonium iodide , lead iodide\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"296.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1180,\n        \"id\": 300,\n        \"compound_name\": \"Bis(naphthaleneoxypropylammonium) lead iodide\",\n        \"formula\": \"(C13H16ON)2PbI4\",\n        \"group\": \"(Nap-O-Pr-NH3)2PbI4, (naphthalene-O-propyl-NH3)2PbI4, bis(naphthaleneoxypropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C13H16ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxypropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Dichloromethane, \\u03b3-butyrolactone (GBL), naphthaleneoxypropylammonium iodide, lead iodide\",\n        \"synthesis_product\": \"Yellow plate-like crystals\",\n        \"synthesis_description\": \"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"299.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1181,\n        \"id\": 301,\n        \"compound_name\": \"Bis(naphthaleneoxypropylammonium) lead iodide\\u00b7\\u03b3-butyrolactone\",\n        \"formula\": \"(C4H6O2)0.5(C13H16ON)2PbI4, C28H35O3N2PbI4\",\n        \"group\": \"(Nap-O-Pr-NH3)2PbI4\\u00ac\\u2211(C4H6O2)0.5, bis(naphthalene-O-propyl-NH3) tetraiodoplumbate(II)\",\n        \"organic\": \"C4H6O2,C13H16ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"Bis(naphthaleneoxypropylammonium) lead (II) iodide\\u00b7\\u03b3-butyrolactone\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Dichloromethane, \\u03b3-butyrolactone (GBL), naphthaleneoxypropylammonium iodide, lead iodide\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"299.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1182,\n        \"id\": 302,\n        \"compound_name\": \"Bis(pyreneoxyethylammonium) lead iodide\",\n        \"formula\": \"(C18H16ON)2PbI4, C36H32O2N2PbI4\",\n        \"group\": \"(pyrene-O-ethyl-NH3)2PbI4, bis(pyreneoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C18H16ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pyreneoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Dichloromethane, \\u03b3-butyrolactone (GBL), pyreneoxyethylammonium iodide, lead iodide\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"299.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1183,\n        \"id\": 303,\n        \"compound_name\": \"Bis(pyreneoxypropylammonium) lead iodide\",\n        \"formula\": \"(C19H18ON)2PbI4\",\n        \"group\": \"(pyrene-O-propyl-NH3)2PbI4, bis(pyreneoxypropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C19H18ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pyreneoxypropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Dichloromethane, \\u03b3-butyrolactone (GBL), pyreneoxypropylammonium iodide, lead iodide\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"299.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1184,\n        \"id\": 304,\n        \"compound_name\": \"Bis(pyreneoxybutylammonium) lead iodide\",\n        \"formula\": \"(C20H20ON)2PbI4\",\n        \"group\": \"(pyrene-O-butyl-NH3)2PbI4, bis(pyreneoxybutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C20H20ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pyreneoxybutylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Dichloromethane, \\u03b3-butyrolactone (GBL), pyreneoxybutylammonium iodide, lead iodide\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"299.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1185,\n        \"id\": 305,\n        \"compound_name\": \"Bis(perylenoxyethylammonium) lead iodide\",\n        \"formula\": \"(C22H18ON)2PbI4\",\n        \"group\": \"(perylene-O-ethyl-NH3)2PbI4, bis(perylenoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C22H18ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(perylenoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Dichloromethane, \\u03b3-butyrolactone (GBL), perylenoxyethylammonium iodide, lead iodide\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"a 2:1 molar ratio solution of the organic ammonium iodide salt to the lead iodide was prepared in gamma-butyrolactone. Dichloromethane was then vapor diffused into the solution, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"299.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1186,\n        \"id\": 299,\n        \"compound_name\": \"Bis(naphthaleneoxyethylammonium) lead iodide\",\n        \"formula\": \"(C12H14ON)2PbI4, C24H28O2N2PbI4\",\n        \"group\": \"(Nap-O-Et-NH3)2PbI4, (naphthalene-O-ethyl-NH3)2PbI4, bis(naphthaleneoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C12H14ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"naphthaleneoxyethylammonium iodide salt, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1187,\n        \"id\": 300,\n        \"compound_name\": \"Bis(naphthaleneoxypropylammonium) lead iodide\",\n        \"formula\": \"(C13H16ON)2PbI4\",\n        \"group\": \"(Nap-O-Pr-NH3)2PbI4, (naphthalene-O-propyl-NH3)2PbI4, bis(naphthaleneoxypropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C13H16ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxypropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"naphthaleneoxypropylammonium iodide, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1188,\n        \"id\": 302,\n        \"compound_name\": \"Bis(pyreneoxyethylammonium) lead iodide\",\n        \"formula\": \"(C18H16ON)2PbI4, C36H32O2N2PbI4\",\n        \"group\": \"(pyrene-O-ethyl-NH3)2PbI4, bis(pyreneoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C18H16ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pyreneoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"pyreneoxyethylammonium iodide, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1189,\n        \"id\": 303,\n        \"compound_name\": \"Bis(pyreneoxypropylammonium) lead iodide\",\n        \"formula\": \"(C19H18ON)2PbI4\",\n        \"group\": \"(pyrene-O-propyl-NH3)2PbI4, bis(pyreneoxypropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C19H18ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pyreneoxypropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"pyreneoxypropylammonium iodide, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1190,\n        \"id\": 304,\n        \"compound_name\": \"Bis(pyreneoxybutylammonium) lead iodide\",\n        \"formula\": \"(C20H20ON)2PbI4\",\n        \"group\": \"(pyrene-O-butyl-NH3)2PbI4, bis(pyreneoxybutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C20H20ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pyreneoxybutylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"pyreneoxybutylammonium iodide, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Kappa Apex 3 diffractometer was used to collect SCXRD data. Within the Olex 2 software package, ShelXS was used to solve the structure and ShelXL was used to refine it with least-squares minimizations.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1191,\n        \"id\": 305,\n        \"compound_name\": \"Bis(perylenoxyethylammonium) lead iodide\",\n        \"formula\": \"(C22H18ON)2PbI4\",\n        \"group\": \"(perylene-O-ethyl-NH3)2PbI4, bis(perylenoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C22H18ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(perylenoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"perylenoxyethylammonium iodide, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to perform the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1192,\n        \"id\": 299,\n        \"compound_name\": \"Bis(naphthaleneoxyethylammonium) lead iodide\",\n        \"formula\": \"(C12H14ON)2PbI4, C24H28O2N2PbI4\",\n        \"group\": \"(Nap-O-Et-NH3)2PbI4, (naphthalene-O-ethyl-NH3)2PbI4, bis(naphthaleneoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C12H14ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"naphthaleneoxyethylammonium iodide, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba Nanolog Fluorimeter instrument was used to measure the steady-state PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b03659\",\n        \"dataset_ID\": 1193,\n        \"id\": 300,\n        \"compound_name\": \"Bis(naphthaleneoxypropylammonium) lead iodide\",\n        \"formula\": \"(C13H16ON)2PbI4\",\n        \"group\": \"(Nap-O-Pr-NH3)2PbI4, (naphthalene-O-propyl-NH3)2PbI4, bis(naphthaleneoxypropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C13H16ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxypropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhanced Out-of-Plane Conductivity and Photovoltaic Performance in n = 1 Layered Perovskites through Organic Cation Design\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"7313\",\n        \"pages_end\": \"7323\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"naphthaleneoxypropylammonium iodide, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"a 2:1 molar ratio of the organic ammonium iodide salt to the lead iodide was dissolved in a 50/50 (v/v) DMF/DMSO solution and spin-coated onto glass slides at a spin rate of 2000 rpm. Afterward, they were annealed on a hot plate at 110 degrees Celsius for 30 minutes.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba Nanolog Fluorimeter instrument was used to measure the steady-state PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.0c00371\",\n        \"dataset_ID\": 1194,\n        \"id\": 308,\n        \"compound_name\": \"Piperidinium lead iodide\",\n        \"formula\": \"(C5H12N)PbI3\",\n        \"group\": \"(piperidinium)PbI3, (PD)PbI3, piperidinium triiodoplumbate(II)\",\n        \"organic\": \"C5H12N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observation of Vortex Domains in a Two-Dimensional Lead Iodide Perovskite Ferroelectric\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"4952\",\n        \"pages_end\": \"4931\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, piperidinium hydrochloride, HI (47 wt % in water)\",\n        \"synthesis_product\": \"yellow prismatic crystals\",\n        \"synthesis_description\": \"PbI2 (0.92 g, 2 mmol) and piperidinium hydrochloride (0.63 g, 2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were recorded using a Rigaku Saturn 724+ CCD diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"300.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1199,\n        \"id\": 311,\n        \"compound_name\": \"Bis(naphthaleneoxybutylammonium) lead iodide\",\n        \"formula\": \"(C14H18ON)2PbI4, C28H36O2N2PbI4\",\n        \"group\": \"(Nap-O-Bu-NH3)2PbI4, (naphthalene-O-butyl-NH3)2PbI4, bis(naphthaleneoxybutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C14H18ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxybutylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",\n        \"synthesis_product\": \"Plate-like crystals\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\",\n        \"physical_property\": \"273.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pca2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1200,\n        \"id\": 312,\n        \"compound_name\": \"Bis(naphthaleneoxyhexylammonium) lead iodide\",\n        \"formula\": \"(C16H22ON)2PbI4\",\n        \"group\": \"(Nap-O-Hex-NH3)2PbI4, (naphthalene-O-hexyl-NH3)2PbI4, bis(naphthaleneoxyhexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C16H22ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(naphthaleneoxyhexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",\n        \"synthesis_product\": \"Plate-like crystals\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\",\n        \"physical_property\": \"300.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1201,\n        \"id\": 313,\n        \"compound_name\": \"Bis(5-methoxynaphthaleneoxyethylammonium) lead iodide\",\n        \"formula\": \"(C13H16O2N)2PbI4\",\n        \"group\": \"(MeO-Nap-O-Et-NH3)2PbI4, (methoxy-naphthalene-O-ethyl-NH3)2PbI4, bis(methoxynaphthaleneoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C13H16O2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-methoxynaphthaleneoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",\n        \"synthesis_product\": \"Plate-like crystals\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\",\n        \"physical_property\": \"296.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1202,\n        \"id\": 314,\n        \"compound_name\": \"Bis(5-methoxynaphthaleneoxybutylammonium) lead iodide\",\n        \"formula\": \"(C15H20O2N)2PbI4\",\n        \"group\": \"(MeO-Nap-O-Bu-NH3)2PbI4, (methoxy-naphthalene-O-butyl-NH3)2PbI4, bis(methoxynaphthaleneoxybutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C15H20O2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-methoxynaphthaleneoxybutylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",\n        \"synthesis_product\": \"Plate-like crystals\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter.  100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\",\n        \"physical_property\": \"299.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbcn\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1203,\n        \"id\": 315,\n        \"compound_name\": \"Bis(5-methoxynaphthaleneoxyhexylammonium) lead iodide\",\n        \"formula\": \"(C17H24O2N)2PbI4\",\n        \"group\": \"(MeO-Nap-O-Hex-NH3)2PbI4, (methoxy-naphthalene-O-hexyl-NH3)2PbI4, bis(methoxynaphthaleneoxyhexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C17H24O2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-methoxynaphthaleneoxyhexylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",\n        \"synthesis_product\": \"Plate-like crystals\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\",\n        \"physical_property\": \"299.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1204,\n        \"id\": 316,\n        \"compound_name\": \"Bis(pentachloro-phenyloxypropylammonium) lead iodide\",\n        \"formula\": \"(Cl5C9H9ON)2PbI4\",\n        \"group\": \"(C6Cl5-O-Pr-NH3)2PBI4, (C6Cl5-O-propyl-NH3)2PbI4, bis(pentachloro-phenyloxypropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"Cl5C9H9ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pentachloro-phenyloxypropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide\",\n        \"synthesis_product\": \"Plate-like crystals\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Kappa Apex3 diffractometer was used at room temperature to perform SCXRD. The ShelXS and ShelXT programs were used to solve the structure, and the ShelXL refinement program was used to refine it, all within the Olex2 software package.\",\n        \"physical_property\": \"300.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1205,\n        \"id\": 313,\n        \"compound_name\": \"Bis(5-methoxynaphthaleneoxyethylammonium) lead iodide\",\n        \"formula\": \"(C13H16O2N)2PbI4\",\n        \"group\": \"(MeO-Nap-O-Et-NH3)2PbI4, (methoxy-naphthalene-O-ethyl-NH3)2PbI4, bis(methoxynaphthaleneoxyethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C13H16O2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-methoxynaphthaleneoxyethylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours. The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1206,\n        \"id\": 314,\n        \"compound_name\": \"Bis(5-methoxynaphthaleneoxybutylammonium) lead iodide\",\n        \"formula\": \"(C15H20O2N)2PbI4\",\n        \"group\": \"(MeO-Nap-O-Bu-NH3)2PbI4, (methoxy-naphthalene-O-butyl-NH3)2PbI4, bis(methoxynaphthaleneoxybutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C15H20O2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-methoxynaphthaleneoxybutylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours.  The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1207,\n        \"id\": 315,\n        \"compound_name\": \"Bis(5-methoxynaphthaleneoxyhexylammonium) lead iodide\",\n        \"formula\": \"(C17H24O2N)2PbI4\",\n        \"group\": \"(MeO-Nap-O-Hex-NH3)2PbI4, (methoxy-naphthalene-O-hexyl-NH3)2PbI4, bis(methoxynaphthaleneoxyhexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C17H24O2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(5-methoxynaphthaleneoxyhexylaminium) lead (II) iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours. The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41557-020-0488-2\",\n        \"dataset_ID\": 1208,\n        \"id\": 316,\n        \"compound_name\": \"Bis(pentachloro-phenyloxypropylammonium) lead iodide\",\n        \"formula\": \"(Cl5C9H9ON)2PbI4\",\n        \"group\": \"(C6Cl5-O-Pr-NH3)2PBI4, (C6Cl5-O-propyl-NH3)2PbI4, bis(pentachloro-phenyloxypropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"Cl5C9H9ON\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pentachloro-phenyloxypropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable exciton binding energy in 2D hybrid layered perovskites through donor\\u2013acceptor interactions within the organic layer\",\n        \"journal\": \"Nature Chemistry\",\n        \"vol\": \"12\",\n        \"pages_start\": \"672\",\n        \"pages_end\": \"682\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Dichloromethane (DCM), \\u03b3-butyrolactone (GBL), organic ammonium iodide salt, lead iodide, DMF, DMSO\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 2:1 molar ratio of the organic ammonium iodide salt:lead iodide was dissolved in \\u03b3-butyrolactone. The solution was filtered through a 0.45-\\u00b5m polytetrafluoroethylene filter. 100\\u2009\\u00b5l of the filtrate was taken in a 1.5\\u2009ml glass vial. The vial was sealed inside a 20 mL vial with 2-5 mL DCM, causing crystals to precipitate within 24 hours. The crystals were first dissolved in 50/50 DMF and DMSO at 60 degrees Celsius for 20 minutes. The solutions were then cooled and spin-coated onto glass slides at the spin rate of 2000 rpm, followed by annealing on a hot plate at 100 degrees Celsius for 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A PerkinElmer LAMBDA 1050 instrument was used to directly measure the UV-vis absorption spectroscopy.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1209,\n        \"id\": 317,\n        \"compound_name\": \"Bis(butylammonium) tin iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2SnI4\",\n        \"group\": \"(BA)2SnI4, (C4)2SnI4, bis(butylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(butylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, Ethanol, SnI2, butylammonium iodide (BAI)\",\n        \"synthesis_product\": \"dark purple plate-like crystals\",\n        \"synthesis_description\": \"In an inert atmosphere, stoichiometric quantities of BAI and SnI2 were added to HI. The solution was heated to 75\\u00b0C to dissolve the solids and subsequently cooled to 5 \\u00b0C at a rate of 1.5 \\u00b0C/hour.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"128.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1210,\n        \"id\": 318,\n        \"compound_name\": \"Pentyldiammonium tin iodide\",\n        \"formula\": \"NH3(CH2)5NH3SnI4\",\n        \"group\": \"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"pentyldiaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Black plate-like crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"273.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1211,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Dark plate-like crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"203.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1212,\n        \"id\": 319,\n        \"compound_name\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"formula\": \"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",\n        \"group\": \"(TRA)2 tetraiodostannate(II)\",\n        \"organic\": \"C16H32N2O4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Brown plate-like crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"293.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1213,\n        \"id\": 320,\n        \"compound_name\": \"Bis(iodobutylammonium) tin iodide\",\n        \"formula\": \"(I(CH2)4NH3)2SNI4\",\n        \"group\": \"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H22N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(iodobutylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"295.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1214,\n        \"id\": 321,\n        \"compound_name\": \"Bis(4-aminobutyric acid) tin iodide\",\n        \"formula\": \"(HOOC(CH2)3NH3)2SnI4\",\n        \"group\": \"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",\n        \"organic\": \"C4NO2H10\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(4-aminiumbutanoic acid) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Brown plate-like crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"273.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1215,\n        \"id\": 322,\n        \"compound_name\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"formula\": \"(C5H10N)C2H4NH2\",\n        \"group\": \"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",\n        \"organic\": \"C7H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"296.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1216,\n        \"id\": 323,\n        \"compound_name\": \"3-iodopyridinium tin iodide\",\n        \"formula\": \"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\n        \"group\": \"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",\n        \"organic\": \"IC5H5N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3-iodopyridinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Brown plate-like crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using a Rigaku R-AXIS rapid imaging plate diffractometer with graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71069 \\u00c5).\",\n        \"physical_property\": \"293.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1217,\n        \"id\": 317,\n        \"compound_name\": \"Bis(butylammonium) tin iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2SnI4\",\n        \"group\": \"(BA)2SnI4, (C4)2SnI4, bis(butylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(butylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1218,\n        \"id\": 318,\n        \"compound_name\": \"Pentyldiammonium tin iodide\",\n        \"formula\": \"NH3(CH2)5NH3SnI4\",\n        \"group\": \"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"pentyldiaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1219,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1220,\n        \"id\": 319,\n        \"compound_name\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"formula\": \"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",\n        \"group\": \"(TRA)2 tetraiodostannate(II)\",\n        \"organic\": \"C16H32N2O4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1221,\n        \"id\": 320,\n        \"compound_name\": \"Bis(iodobutylammonium) tin iodide\",\n        \"formula\": \"(I(CH2)4NH3)2SNI4\",\n        \"group\": \"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H22N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(iodobutylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1222,\n        \"id\": 321,\n        \"compound_name\": \"Bis(4-aminobutyric acid) tin iodide\",\n        \"formula\": \"(HOOC(CH2)3NH3)2SnI4\",\n        \"group\": \"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",\n        \"organic\": \"C4NO2H10\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(4-aminiumbutanoic acid) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1223,\n        \"id\": 322,\n        \"compound_name\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"formula\": \"(C5H10N)C2H4NH2\",\n        \"group\": \"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",\n        \"organic\": \"C7H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1224,\n        \"id\": 323,\n        \"compound_name\": \"3-iodopyridinium tin iodide\",\n        \"formula\": \"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\n        \"group\": \"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",\n        \"organic\": \"IC5H5N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3-iodopyridinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"CAESER Software Suite\",\n        \"level_of_theory\": \"Semiempirical model: Extended Huckel Method\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1227,\n        \"id\": 317,\n        \"compound_name\": \"Bis(butylammonium) tin iodide\",\n        \"formula\": \"(CH3(CH2)3NH3)2SnI4\",\n        \"group\": \"(BA)2SnI4, (C4)2SnI4, bis(butylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H24N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(butylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Room temperature resistivity: 10 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1229,\n        \"id\": 318,\n        \"compound_name\": \"Pentyldiammonium tin iodide\",\n        \"formula\": \"NH3(CH2)5NH3SnI4\",\n        \"group\": \"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"pentyldiaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe method\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Room temperature resistivity: 20 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1230,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe method\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Room temperature resistivity: 40 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1231,\n        \"id\": 319,\n        \"compound_name\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"formula\": \"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",\n        \"group\": \"(TRA)2 tetraiodostannate(II)\",\n        \"organic\": \"C16H32N2O4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe method\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Room temperature resistivity: 50 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1232,\n        \"id\": 320,\n        \"compound_name\": \"Bis(iodobutylammonium) tin iodide\",\n        \"formula\": \"(I(CH2)4NH3)2SNI4\",\n        \"group\": \"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H22N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(iodobutylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe method\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Room temperature resistivity: 900 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1234,\n        \"id\": 321,\n        \"compound_name\": \"Bis(4-aminobutyric acid) tin iodide\",\n        \"formula\": \"(HOOC(CH2)3NH3)2SnI4\",\n        \"group\": \"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",\n        \"organic\": \"C4NO2H10\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(4-aminiumbutanoic acid) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe method\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Room temperature resistivity: 600 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1235,\n        \"id\": 322,\n        \"compound_name\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"formula\": \"(C5H10N)C2H4NH2\",\n        \"group\": \"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",\n        \"organic\": \"C7H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe method\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Room temperature resistivity: 2000 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1236,\n        \"id\": 323,\n        \"compound_name\": \"3-iodopyridinium tin iodide\",\n        \"formula\": \"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\n        \"group\": \"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",\n        \"organic\": \"IC5H5N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3-iodopyridinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"resistivity\",\n        \"primary_unit\": \"ln(rho [ohms-cm])\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe method\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Room temperature resistivity: 10E7 ohms-cm\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1237,\n        \"id\": 318,\n        \"compound_name\": \"Pentyldiammonium tin iodide\",\n        \"formula\": \"NH3(CH2)5NH3SnI4\",\n        \"group\": \"(C5di)SnI4, 1-pentylammonium tin iodide, pentyldiaminium tetraiodostannate(II)\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"pentyldiaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. \\r\\n\\r\\nValues extracted from fitting equation 1 in the article to the resistivity data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1238,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1239,\n        \"id\": 319,\n        \"compound_name\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"formula\": \"C16H32N2O4SnI4, (HOOC(C6H10)CH2NH3)2SnI4\",\n        \"group\": \"(TRA)2 tetraiodostannate(II)\",\n        \"organic\": \"C16H32N2O4\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"Bis((4-carboxycyclohexyl)methanaminium) tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1240,\n        \"id\": 320,\n        \"compound_name\": \"Bis(iodobutylammonium) tin iodide\",\n        \"formula\": \"(I(CH2)4NH3)2SNI4\",\n        \"group\": \"(IC4)2SnI4, 1-iodobutylammonium tin iodide, (I-BA)2SnI4, bis(iodobutylaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H22N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(iodobutylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1241,\n        \"id\": 321,\n        \"compound_name\": \"Bis(4-aminobutyric acid) tin iodide\",\n        \"formula\": \"(HOOC(CH2)3NH3)2SnI4\",\n        \"group\": \"(GABA)2SnI4, 4-aminobutyric acid tin iodide, gamma-aminobutyric acid tin iodide, bis(4-aminiumbutanoic acid) tetraiodostannate(II)\",\n        \"organic\": \"C4NO2H10\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(4-aminiumbutanoic acid) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1242,\n        \"id\": 322,\n        \"compound_name\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"formula\": \"(C5H10N)C2H4NH2\",\n        \"group\": \"(AEPi)SnI4, 1-(aminoethyl)piperdinium tin iodide, 1-(aminoethyl)piperdinium tetraiodostannate(II)\",\n        \"organic\": \"C7H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"1-(aminoethyl)piperdinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm702405c\",\n        \"dataset_ID\": 1243,\n        \"id\": 323,\n        \"compound_name\": \"3-iodopyridinium tin iodide\",\n        \"formula\": \"C10H10N2SnI6, (I(C5H4)NH)2SnI4\",\n        \"group\": \"(IPy)2SnI4, 3-iodopyridinium tin iodide, 3-iodopyridinium tetraiodostannate(II)\",\n        \"organic\": \"IC5H5N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"3-iodopyridinium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Charge Transport in Soluble Organic\\u2013Inorganic Hybrid Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"6312\",\n        \"pages_end\": \"6316\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"HI, H3PO2, anhydrous ethanol, SnI2, organic cation iodide salt\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"Stoichiometric ratios of purified SnI2 and the organic cation iodide salt were added to either an HI or ethanol solution in an inert atmosphere. The solids were fully dissolved by raising the ethanol solutions to 65 degrees Celsius and the HI solutions to 75 degrees. The solutions were then cooled at the rate of 1.5 degrees per hour until 5 degrees was reached, over which time crystals precipitated.\",\n        \"experimental_method\": \"Four-probe DC conductivity\",\n        \"experimental_description\": \"The standard four-probe method was used to measure the DC conductivity. Carbon paste was applied over the sample to mount two gold wires on either end of the sample as the current source. The two remaining wires, the voltage probes, were attached to the surface also via the carbon paste. The sample was kept in vacuum over the duration of the experiments, over the temperature range 5 to 300 K. Values extracted from fitting equation 1 in the article to the resistivity data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b02208\",\n        \"dataset_ID\": 1246,\n        \"id\": 325,\n        \"compound_name\": \"Bis(hexylammonium) copper chloride\",\n        \"formula\": \"(C6H13NH3)2CuCl4\",\n        \"group\": \"C6MnCl, bis(hexylaminium) tetrachloromanganate(II)\",\n        \"organic\": \"C6NH16\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"bis(hexylaminium) copper chloride\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Medium Dependent Solid-Solid Phase Transformations in 2D Hybrid Perovskites\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"28\",\n        \"pages_start\": \"5522\",\n        \"pages_end\": \"5529\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"hydrochloric acid (37%), hexylamine, ethanol, diethyl ether, CuCl2.2H2O\",\n        \"synthesis_product\": \"Yellow plate-like crystals\",\n        \"synthesis_description\": \"Hexylammonium chloride was synthesized by reacting HCl (5.85 mL, 70.00 mmol) with a cold stirred solution of hexylamine (9.34 mL, 70.00 mmol) 10 mL in ethanol. The solvent was evaporated using a rotary evaporator at 60 degrees C, and the obtained solid was washed with diethyl ether and dried overnight.\\r\\n3.90 mmol of hexylammonium chloride and 1.95 mmol of CuCl2 were dissolved in 2.5 mL of water by heating. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using a Bruker DUO diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.710\\u202f73 \\u00c5) and an APEXII CCD area detector\",\n        \"physical_property\": \"233.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1248,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"Pb(NO3)2, KBr, HBr (48% aqueous), CsBr, ethanol (EtOH)\",\n        \"synthesis_product\": \"orange, transparent crystals\",\n        \"synthesis_description\": \"PbBr2 was first synthesized by dissolving Pb(NO3)2 (0.15 mol, 49.6 g) in 100 mL of boiling H2O. Meanwhile, KBr (0.3 mol, 35.7 g) was dissolved in 50 mL of H2O in a separate beaker and then slowly added to the Pb(NO3)2 solution with constant stirring. As a result, PbBr2 immediately precipitated and after 15 minutes of stirring, the solution was cooled to room temperature. The PbBr2 was filtered under vacuum, washed with distilled water, and dried overnight. This product was used in the synthesis of CsPbBr3. The PbBr2 (20 mmol, 7.31 g) was dissolved in 30 mL of HBr (48% wt.). A pale, yellow solution resulted, and CsBr (20 mmol, 4.26 mg) was dissolved in 10 mL of H2O. A bright orange solid immediately precipitated. The solid was suction filtered, washed with EtOH, dried under vacuum. Finally, the Bridgeman Method was performed to obtain single crystals. 6g of CsPbBr3 were ground with mortar and pestle, placed in a silica tub (OD/ID: 9mm/7mm), and the tube compilation was brought to a 10^{-4} mbar vacuum and flame-sealed. Then, the ampoule was attached to a clock mechanism, lowered into a 3-zone vertical tube furnace (temperature gradient: 10\\u00ba C/mm). Dropping speed varied from 3 to 30 mm/h.\",\n        \"experimental_method\": \"Single Crystal X-ray diffraction\",\n        \"experimental_description\": \"STOE IPDS II or IPDS 2T diffractometer were used. Mo K\\u03b1 radiation (\\u03bb= 0.71073 \\u00c5) was performed, and diffractometers were operating at 50 kV and 40 mA. Absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs. Structures were solved directly and refined by full matrix least squares on F2 with the SHELXTL program package. Rotax functions of PLATON software (in WINGX platform) were used to find correct space group.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1249,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH),\",\n        \"synthesis_product\": \"Orange transparent crystals\",\n        \"synthesis_description\": \"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. \\r\\n6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"The spectrum was recorded using a Shimadzu UV-3101 PC double-beam, double monochromator spectrophotometer. Tauc plot with direct band gap assumption was used to obtain the band gap.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1251,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",\n        \"synthesis_product\": \"Orange transparent crystals\",\n        \"synthesis_description\": \"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. 6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Low temperature PL measurements were performed on polished, etched samples. Excitation source was He-Cd (325 nm) or N2 (337nm) laser. Spectrum was analyzed with 0.75-m SPEX grating monochromator. Signal was detected with R928 Hamamatsu photomultiplier tube (PMT) and phase sensitive detection lock-in system.\",\n        \"physical_property\": \"46.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1252,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Scattering Intensity\",\n        \"primary_unit\": \"cps\",\n        \"secondary_name\": \"Raman Shift\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",\n        \"synthesis_product\": \"Orange transparent crystals\",\n        \"synthesis_description\": \"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. 6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",\n        \"experimental_method\": \"Raman spectroscopy\",\n        \"experimental_description\": \"DeltaNu Advantage NIR spectrometer was used with 785 nm irradiation and a CCD camera detector with backscattered setup. Max power of 60 mW and beam diameter of 35 \\u03bcm were used. Spectra was collected with integration times of 0.1-1 s.\",\n        \"physical_property\": \"785.0\",\n        \"unit\": \"nm\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1255,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"a.u\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",\n        \"synthesis_product\": \"Orange transparent crystals\",\n        \"synthesis_description\": \"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum. 6 g of CsPbBr3 powder was finely ground and loaded in a silica tube. Following this Bridgman method was applied to grow the crystals in a 3-zone vertical tube furnace.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Low temperature PL measurements were performed on polished, etched samples. Excitation source was He-Cd (325 nm) or N2 (337nm) laser. Spectrum was analyzed with 0.75-m SPEX grating monochromator. Signal was detected with R928 Hamamatsu photomultiplier tube (PMT) and phase sensitive detection lock-in system.\",\n        \"physical_property\": \"46.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1256,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Low temperature PL measurements were performed on polished, etched samples. Excitation source was He-Cd (325 nm) or N2 (337nm) laser. Spectrum was analyzed with 0.75-m SPEX grating monochromator. Signal was detected with R928 Hamamatsu photomultiplier tube (PMT) and phase sensitive detection lock-in system.\",\n        \"physical_property\": \"110.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1257,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"cm^{-2}\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were executed at 298 K with a Shimadzu UV-3101 PC double-beam, double monochromator spectrophotometer between 200 to 2500 nm. One Nicolet 6700 IR spectrometer with a diffuse-reflectance kit was used for 4000-400cm^{-1} region. The reflectance vs. wavelength data was used to convert the data to absorption data via the Kubelka-Munk equation: \\u03b1/S = (1-R)^2/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cg400645t\",\n        \"dataset_ID\": 1258,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection\",\n        \"journal\": \"Crystal Growth and Design\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2722\",\n        \"pages_end\": \"2727\",\n        \"year\": \"2013\",\n        \"synthesis_starting_materials\": \"PbBr2 (synthesized), HBr (48% aqueous), CsBr, ethanol (EtOH)\",\n        \"synthesis_product\": \"Orange powder\",\n        \"synthesis_description\": \"PbBr2 (7.31 g, 20 mmol) was dissolved in 30 mL HBr solution, and CsBr (4.26 mg, 20 mmol) was dissolved in 10 ml of H2O. Both of these solutions were mixed at room temperature. The obtained orange powder (CsPbBr3) was filtered, washed with EtOH, and dried under a vacuum.\",\n        \"experimental_method\": \"UV-vis absorbance (diffuse reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were executed at 298 K with a Shimadzu UV-3101 PC double-beam, double monochromator spectrophotometer between 200 to 2500 nm. One Nicolet 6700 IR spectrometer with a diffuse-reflectance kit was used for 4000-400cm^{-1} region. The reflectance vs. wavelength data was used to convert the data to absorption data via the Kubelka-Munk equation: \\u03b1/S = (1-R)^2/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja301539s\",\n        \"dataset_ID\": 1259,\n        \"id\": 327,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"CsSnI3\",\n        \"group\": \"Cesium triiodostannate(II), CsSnI3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CsSnI3: Semiconductor or Metal? High Electrical Conductivity and Strong Near-Infrared Photoluminescence from a Single Material. High Hole Mobility and Phase-Transitions\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"134\",\n        \"pages_start\": \"8579\",\n        \"pages_end\": \"8587\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"CsI, SnI2\",\n        \"synthesis_product\": \"black crystals\",\n        \"synthesis_description\": \"A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 \\u00baC for 60 minutes. The mixture then cooled for 6 hours to room temperature.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an STOE IPDS 2T diffractometer. Mo K\\u03b1 radiation (50 kV, 40 mA, 34 cm diameter imaging plate) was used. Frames were collected with a 3 min exposure time and 1.0\\u03c9 rotation. Absorption corrections, data extractions, and integrations were performed with X-AREA, X-RED, and X-SHAPE. Finally, the SHELXTL software package was used to refine/solve the structure.\",\n        \"physical_property\": \"500.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Pm-3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja301539s\",\n        \"dataset_ID\": 1260,\n        \"id\": 327,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"CsSnI3\",\n        \"group\": \"Cesium triiodostannate(II), CsSnI3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CsSnI3: Semiconductor or Metal? High Electrical Conductivity and Strong Near-Infrared Photoluminescence from a Single Material. High Hole Mobility and Phase-Transitions\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"134\",\n        \"pages_start\": \"8579\",\n        \"pages_end\": \"8587\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"CsI, SnI2\",\n        \"synthesis_product\": \"black crystals\",\n        \"synthesis_description\": \"A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 \\u00baC for 60 minutes. The mixture then cooled for 6 hours to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"The spectrum was recorded using a Shimadzu UV-3101 PC spectrometer. The reflectance data was converted to absorbance using the Kubelka-Munk equation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja301539s\",\n        \"dataset_ID\": 1261,\n        \"id\": 327,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"CsSnI3\",\n        \"group\": \"Cesium triiodostannate(II), CsSnI3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CsSnI3: Semiconductor or Metal? High Electrical Conductivity and Strong Near-Infrared Photoluminescence from a Single Material. High Hole Mobility and Phase-Transitions\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"134\",\n        \"pages_start\": \"8579\",\n        \"pages_end\": \"8587\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"CsI, SnI2\",\n        \"synthesis_product\": \"black crystals (orthorhombic phase)\",\n        \"synthesis_description\": \"A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 \\u00baC for 60 minutes. The mixture then cooled for 6 hours to room temperature.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja301539s\",\n        \"dataset_ID\": 1262,\n        \"id\": 327,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"CsSnI3\",\n        \"group\": \"Cesium triiodostannate(II), CsSnI3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Conductivity\",\n        \"primary_unit\": \"S\\u2022cm^{-1}\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CsSnI3: Semiconductor or Metal? High Electrical Conductivity and Strong Near-Infrared Photoluminescence from a Single Material. High Hole Mobility and Phase-Transitions\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"134\",\n        \"pages_start\": \"8579\",\n        \"pages_end\": \"8587\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"CsI, SnI2\",\n        \"synthesis_product\": \"black crystals (orthorhombic phase)\",\n        \"synthesis_description\": \"A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 \\u00baC for 60 minutes. The mixture was then cooled for 6 hours to room temperature.\",\n        \"experimental_method\": \"Electrical conductivity\",\n        \"experimental_description\": \"Ingots were cut to the size of ~2mm x 3 mm x 8 mm in N2. These samples were then cut into rectangles. These samples were measured under He atmosphere in temperatures ranging from 300 K to 650 K. A ULVAC-RIKO ZEM-3 instrument system was used. Mechanical electrodes made of Rh-Pt and Pt made direct contact with ingot (no chemical paste).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja301539s\",\n        \"dataset_ID\": 1263,\n        \"id\": 327,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"CsSnI3\",\n        \"group\": \"Cesium triiodostannate(II), CsSnI3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CsSnI3: Semiconductor or Metal? High Electrical Conductivity and Strong Near-Infrared Photoluminescence from a Single Material. High Hole Mobility and Phase-Transitions\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"134\",\n        \"pages_start\": \"8579\",\n        \"pages_end\": \"8587\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"CsI, SnI2\",\n        \"synthesis_product\": \"yellow crystals\",\n        \"synthesis_description\": \"A stoichiometric mixture of CsI and SnI2 (total mass ~ 0.3 g) reacted in ethylenediamine (0.2 mL) in an evacuated Pyrex tube at 140 \\u00baC for 3 days. Then, crack- and bubble-free ingots (~6 g) were prepared via the vertical Bridgeman technique; that is, pure CsSnI3 powder in an evacuated fused silica tube was passed down a single-zone Bridgeman furnace.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"The spectrum was recorded using a Shimadzu UV-3101 PC spectrometer. The reflectance data were converted to absorbance using the Kubelka-Munk equation:: \\u03b1/S = (1-R)^{2}/(2R), where R = reflectance, \\u03b1= absorption coefficient, S = scattering coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja301539s\",\n        \"dataset_ID\": 1264,\n        \"id\": 327,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"CsSnI3\",\n        \"group\": \"Cesium triiodostannate(II), CsSnI3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CsSnI3: Semiconductor or Metal? High Electrical Conductivity and Strong Near-Infrared Photoluminescence from a Single Material. High Hole Mobility and Phase-Transitions\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"134\",\n        \"pages_start\": \"8579\",\n        \"pages_end\": \"8587\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"CsI, SnI2\",\n        \"synthesis_product\": \"black crystals\",\n        \"synthesis_description\": \"A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 \\u00baC for 60 minutes. The mixture then cooled for 6 hours to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Optical diffuse reflectance measurements were executed with a Shimadzu UV-3101 PC spectrometer (operating between 200 and 2500 nm). Reflectance was converted to absorption data with the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/(2R), where R = reflectance, \\u03b1= absorption coefficient, S = scattering coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja301539s\",\n        \"dataset_ID\": 1265,\n        \"id\": 327,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"CsSnI3\",\n        \"group\": \"Cesium triiodostannate(II), CsSnI3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"CsSnI3: Semiconductor or Metal? High Electrical Conductivity and Strong Near-Infrared Photoluminescence from a Single Material. High Hole Mobility and Phase-Transitions\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"134\",\n        \"pages_start\": \"8579\",\n        \"pages_end\": \"8587\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"CsI, SnI2\",\n        \"synthesis_product\": \"black crystals\",\n        \"synthesis_description\": \"A stoichiometric mixture of CsI and SnI2 reacted in an evacuated Pyrex tube at 550 \\u00baC for 60 minutes. The mixture then cooled for 6 hours to room temperature.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1266,\n        \"id\": 328,\n        \"compound_name\": \"Trimethylammonium tin iodide\",\n        \"formula\": \"(CH3)3NHSnI3\",\n        \"group\": \"TMASnI3, trimethanaminium triiodostannate(II)\",\n        \"organic\": \"C3H10N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"trimethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnI2 (synthesized from Sn and I2), (CH3)3N (45% aqueous), HI (99.95% aqueous), and H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"pale yellow needles\",\n        \"synthesis_description\": \"(CH3)3NI was prepared by reacting equimolar amounts of (CH3)3N and HI. The entire reaction was performed under N2 atmosphere. SnI2 (372 mg, 1 mmol) was dissolved in aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M) by heating at 130 \\u00b0C and stirring. To it, (CH3)3NHI (187 mg, 1 mmol) was added. After 5 minutes, the heating and stirring were stopped and the solution was allowed to cool down to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1267,\n        \"id\": 328,\n        \"compound_name\": \"Trimethylammonium tin iodide\",\n        \"formula\": \"(CH3)3NHSnI3\",\n        \"group\": \"TMASnI3, trimethanaminium triiodostannate(II)\",\n        \"organic\": \"C3H10N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"trimethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1268,\n        \"id\": 328,\n        \"compound_name\": \"Trimethylammonium tin iodide\",\n        \"formula\": \"(CH3)3NHSnI3\",\n        \"group\": \"TMASnI3, trimethanaminium triiodostannate(II)\",\n        \"organic\": \"C3H10N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"trimethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnI2 (synthesized from Sn and I2), (CH3)3N (45% aqueous), HI (99.95% aqueous), and H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"pale yellow needles\",\n        \"synthesis_description\": \"(CH3)3NI was prepared by reacting equimolar amounts of (CH3)3N and HI. The entire reaction was performed under N2 atmosphere. SnI2 (372 mg, 1 mmol) was dissolved in aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M) by heating at 130 \\u00b0C and stirring. To it, (CH3)3NHI (187 mg, 1 mmol) was added. After 5 minutes, the heating and stirring were stopped and the solution was allowed to cool down to room temperature.\",\n        \"experimental_method\": \"UV-vis absorbance (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1269,\n        \"id\": 328,\n        \"compound_name\": \"Trimethylammonium tin iodide\",\n        \"formula\": \"(CH3)3NHSnI3\",\n        \"group\": \"TMASnI3, trimethanaminium triiodostannate(II)\",\n        \"organic\": \"C3H10N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"trimethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"SnI2 (synthesized from Sn and I2), (CH3)3N (45% aqueous), HI (99.95% aqueous), and H3PO2 (50% aqueous)\",\n        \"synthesis_product\": \"pale yellow needles\",\n        \"synthesis_description\": \"(CH3)3NI was prepared by reacting equimolar amounts of (CH3)3N and HI. The entire reaction was performed under N2 atmosphere. SnI2 (372 mg, 1 mmol) was dissolved in aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M) by heating at 130 \\u00b0C and stirring. To it, (CH3)3NHI (187 mg, 1 mmol) was added. After 5 minutes, the heating and stirring were stopped, and the solution was allowed to cool down to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1270,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1272\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",\n        \"synthesis_product\": \"pale yellow needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degas the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (173 mg, 1 mmol) was added to the solution. The crystals started appearing in the solution and the solution was held at 120 \\u00b0C for 2 h. Following this, the solution was cooled and the crystals were separated.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1271,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1272,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1270\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",\n        \"synthesis_product\": \"pale yellow needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degas the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (173 mg, 1 mmol) was added to the solution. The crystals started appearing in the solution and the solution was held at 120 \\u00b0C for 2 h. Following this, the solution was cooled and the crystals were separated.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1273,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",\n        \"synthesis_product\": \"Pale yellow, rectangular needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (173 mg, 1 mmol) was added to the solution, which created a dense pale-yellow precipitate. Crystals formed immediately and grew inside the mother liquor for 2 hours at 120\\u00ba C before being washed and collected.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1274,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"Pna2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1275,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"125.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pca2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1276,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P6(3)mc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1277,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (1860 mg, 5 mmol) was dissolved in solution, and the flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (865 mg, 5 mmol) was added to the solution, which created a dense pale-yellow precipitate. The hot plate temperature was raised to 200 \\u00baC, leading to the formation of the dark red metastable phase.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P6(3)mc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1278,\n        \"id\": 329,\n        \"compound_name\": \"Ethylammonium tin iodide\",\n        \"formula\": \"CH3CH2NH3SnI3\",\n        \"group\": \"EASnI3, ethylaminium triiodostannate(II)\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"ethylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3CH2NH3I (synthesized from CH3CH2NH2 (68.0%) and HI)\",\n        \"synthesis_product\": \"dark red crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1860 mg, 5 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3CH2NH3I (865 mg, 5 mmol) was added to the solution, which created a pale-yellow precipitate within 5 minutes. Temperature was raised to 200\\u00ba C, and precipitate changed to dark red.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"125.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pca2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1279,\n        \"id\": 330,\n        \"compound_name\": \"Guanidinium tin iodide\",\n        \"formula\": \"C(NH2)3SnI3\",\n        \"group\": \"GASnI3, diaminomethanaminium triiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"diaminomethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1282\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\n        \"synthesis_product\": \"Orange hexagonal needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 \\u00baC and was held at the same temperature for 2 h.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P63/m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1280,\n        \"id\": 330,\n        \"compound_name\": \"Guanidinium tin iodide\",\n        \"formula\": \"C(NH2)3SnI3\",\n        \"group\": \"GASnI3, diaminomethanaminium triiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"diaminomethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\n        \"synthesis_product\": \"Orange hexagonal needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 \\u00baC and was held at the same temperature for 2 h.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P63/m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1281,\n        \"id\": 330,\n        \"compound_name\": \"Guanidinium tin iodide\",\n        \"formula\": \"C(NH2)3SnI3\",\n        \"group\": \"GASnI3, diaminomethanaminium triiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"diaminomethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\n        \"synthesis_product\": \"Orange hexagonal needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 \\u00baC and was held at the same temperature for 2 h.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1282,\n        \"id\": 330,\n        \"compound_name\": \"Guanidinium tin iodide\",\n        \"formula\": \"C(NH2)3SnI3\",\n        \"group\": \"GASnI3, diaminomethanaminium triiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"diaminomethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1279\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\n        \"synthesis_product\": \"Orange hexagonal needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution. The solution was evaporated to half its volume by boiling at 120 \\u00baC and was held at the same temperature for 2 h.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P63/m\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1283,\n        \"id\": 330,\n        \"compound_name\": \"Guanidinium tin iodide\",\n        \"formula\": \"C(NH2)3SnI3\",\n        \"group\": \"GASnI3, diaminomethanaminium triiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"diaminomethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\n        \"synthesis_product\": \"Dark red (after exposure to air for 30 min, product became black oxidized species).\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (187 mg, 1 mmol) was added to the solution, and the solution was then heated at 120\\u00ba C for 2 hours, then cooled to room temperature.which created a dense pale-yellow precipitate. Solution was stirred for 5 more minutes and then cooled to room temperature.\",\n        \"experimental_method\": \"Dark red (after exposure to air for 30 min, product became black oxidized species).\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1284,\n        \"id\": 330,\n        \"compound_name\": \"Guanidinium tin iodide\",\n        \"formula\": \"C(NH2)3SnI3\",\n        \"group\": \"GASnI3, diaminomethanaminium triiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"diaminomethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\n        \"synthesis_product\": \"red, rectangular crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (750 mg, 4 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. The solution then cooled to room temperature, and crystals grew in the mother liquor for 24 hours.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1285,\n        \"id\": 331,\n        \"compound_name\": \"Bis(guanidinium) tin iodide\",\n        \"formula\": \"{C(NH2)3}2SnI4\",\n        \"group\": \"GA2SnI4, bis(diaminomethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(diaminomethanaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1286,\n        \"id\": 331,\n        \"compound_name\": \"Bis(guanidinium) tin iodide\",\n        \"formula\": \"{C(NH2)3}2SnI4\",\n        \"group\": \"GA2SnI4, bis(diaminomethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(diaminomethanaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/n\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1287,\n        \"id\": 331,\n        \"compound_name\": \"Bis(guanidinium) tin iodide\",\n        \"formula\": \"{C(NH2)3}2SnI4\",\n        \"group\": \"GA2SnI4, bis(diaminomethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(diaminomethanaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"400.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pmna\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1288,\n        \"id\": 330,\n        \"compound_name\": \"Guanidinium tin iodide\",\n        \"formula\": \"C(NH2)3SnI3\",\n        \"group\": \"GASnI3, diaminomethanaminium triiodostannate(II)\",\n        \"organic\": \"CN3H6\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"diaminomethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), C(NH2)3I (synthesized from (C(NH2)3)2CO3 (99%) and HI)\",\n        \"synthesis_product\": \"red, rectangular crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid C(NH2)3I (750 mg, 4 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. The solution then cooled to room temperature, and crystals grew in the mother liquor for 24 hours.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/n\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1289,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\n        \"synthesis_product\": \"orange, hexagonal needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (186 mg, 1 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Crystals began to grow and were left to grow at this temperature for 2 hours. Finally, the solution  was cooled to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1290,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P212121\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1291,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P63cm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1292,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\n        \"synthesis_product\": \"orange, hexagonal needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (186 mg, 1 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Crystals began to grow and were left to grow at this temperature for 2 hours. Finally, the solution  was cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P6(3)mc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1293,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\n        \"synthesis_product\": \"orange, hexagonal needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (186 mg, 1 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Crystals began to grow and were left to grow at this temperature for 2 hours. Finally, the solution  was cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P6(3)mc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1294,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\n        \"synthesis_product\": \"red-orange crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (372 mg, 2 mmol) was added to the solution, and crystals began to grow when stirring was discontinued. Solution cooled, and crystals transformed from red-orange needles to yellow hexagonal plates.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1295,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c/c2121\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1296,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21a\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1297,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\n        \"synthesis_product\": \"red-orange crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (372 mg, 2 mmol) was added to the solution, and crystals began to grow when stirring was discontinued. Solution cooled, and crystals transformed from red-orange needles to yellow hexagonal plates.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1298,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"400.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1299,\n        \"id\": 332,\n        \"compound_name\": \"Acetamidinium tin iodide\",\n        \"formula\": \"CH3C(NH2)2SnI3\",\n        \"group\": \"ACASnI3, Acetamidinium triiodostannate(II)\",\n        \"organic\": \"C2N2H7\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1-aminoethan-1-iminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), CH3C(NH2)2I (synthesized from CH3C(NH2)2Cl (95%) and HI)\",\n        \"synthesis_product\": \"red-orange crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid CH3C(NH2)2I (372 mg, 2 mmol) was added to the solution, and crystals began to grow when stirring was discontinued. Solution cooled, and crystals transformed from red-orange needles to yellow hexagonal plates.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1300,\n        \"id\": 333,\n        \"compound_name\": \"Imidazolium tin iodide\",\n        \"formula\": \"C3N2H5SnI3\",\n        \"group\": \"IMSnI3, imidazolium triiodostannate(II)\",\n        \"organic\": \"C3N2H5\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), imidazole (99%)\",\n        \"synthesis_product\": \"yellow/orange hexagonal plates\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid imidazole (136 mg, 1 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Crystals began to grow for 120\\u00ba C for 2 hours. The solution was then cooled to room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1301,\n        \"id\": 333,\n        \"compound_name\": \"Imidazolium tin iodide\",\n        \"formula\": \"C3N2H5SnI3\",\n        \"group\": \"IMSnI3, imidazolium triiodostannate(II)\",\n        \"organic\": \"C3N2H5\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), imidazole (99%)\",\n        \"synthesis_product\": \"yellow/orange hexagonal plates\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid imidazole (136 mg, 1 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Crystals began to grow for 120\\u00ba C for 2 hours. The solution was then cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1302,\n        \"id\": 333,\n        \"compound_name\": \"Imidazolium tin iodide\",\n        \"formula\": \"C3N2H5SnI3\",\n        \"group\": \"IMSnI3, imidazolium triiodostannate(II)\",\n        \"organic\": \"C3N2H5\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1303,\n        \"id\": 333,\n        \"compound_name\": \"Imidazolium tin iodide\",\n        \"formula\": \"C3N2H5SnI3\",\n        \"group\": \"IMSnI3, imidazolium triiodostannate(II)\",\n        \"organic\": \"C3N2H5\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"400.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1304,\n        \"id\": 333,\n        \"compound_name\": \"Imidazolium tin iodide\",\n        \"formula\": \"C3N2H5SnI3\",\n        \"group\": \"IMSnI3, imidazolium triiodostannate(II)\",\n        \"organic\": \"C3N2H5\",\n        \"inorganic\": \"SnI3, Tin iodide\",\n        \"iupac\": \"1H-imidazol-3-ium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)), imidazole (99%)\",\n        \"synthesis_product\": \"yellow/orange hexagonal plates\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (744 mg, 2 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid imidazole (136 mg, 1 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Crystals began to grow for 120\\u00ba C for 2 hours. The solution was then cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1305,\n        \"id\": 334,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"[(CH3)2CHNH3]3SnI5\",\n        \"group\": \"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",\n        \"synthesis_product\": \"yellow rectangular needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (561 mg, 3 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Stirring stopped, and the solution cool dot room temperature. Crystals precipitated for 24 hours.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1306,\n        \"id\": 334,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"[(CH3)2CHNH3]3SnI5\",\n        \"group\": \"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",\n        \"synthesis_product\": \"yellow rectangular needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (561 mg, 3 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Stirring stopped, and the solution cool dot room temperature. Crystals precipitated for 24 hours.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1307,\n        \"id\": 334,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"[(CH3)2CHNH3]3SnI5\",\n        \"group\": \"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P212121\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1308,\n        \"id\": 334,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"[(CH3)2CHNH3]3SnI5\",\n        \"group\": \"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",\n        \"synthesis_product\": \"yellow rectangular needles\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (372 mg, 1 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (561 mg, 3 mmol) was added to the solution, and the solution was heated to 120\\u00ba C. Stirring stopped, and the solution cool dot room temperature. Crystals precipitated for 24 hours.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1309,\n        \"id\": 334,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"[(CH3)2CHNH3]3SnI5\",\n        \"group\": \"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1116 mg, 3 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (1683 mg, 9 mmol) was added to the solution, and a pale-yellow precipitate formed within 5 minutes. The temperature was raised to 200\\u00ba C, and the precipitate turned red. The solution was cooled and precipitate changed back to yellow.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"P42cm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1310,\n        \"id\": 335,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"{(CH3)2C(H)NH3}3Sn2I7\",\n        \"group\": \"(IPA)3Sn2I7, tris(isopropylaminium) septaiodo distannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"Sn2I7, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"P42cm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1311,\n        \"id\": 335,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"{(CH3)2C(H)NH3}3Sn2I7\",\n        \"group\": \"(IPA)3Sn2I7, tris(isopropylaminium) septaiodo distannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"Sn2I7, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"400.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"I4mm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1312,\n        \"id\": 335,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"{(CH3)2C(H)NH3}3Sn2I7\",\n        \"group\": \"(IPA)3Sn2I7, tris(isopropylaminium) septaiodo distannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"Sn2I7, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ac2a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1313,\n        \"id\": 334,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"[(CH3)2CHNH3]3SnI5\",\n        \"group\": \"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1116 mg, 3 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (1683 mg, 9 mmol) was added to the solution, and a pale-yellow precipitate formed within 5 minutes. The temperature was raised to 200\\u00ba C, and the precipitate turned red. The solution was cooled and precipitate changed back to yellow.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ac2a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1314,\n        \"id\": 334,\n        \"compound_name\": \"Tris(isopropylammonium) tin iodide\",\n        \"formula\": \"[(CH3)2CHNH3]3SnI5\",\n        \"group\": \"(IPA)3SnI5, tris(isopropylaminium) pentaiodostannate(II)\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"SnI5, Tin iodide\",\n        \"iupac\": \"tris(isopropylaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnI2 (synthesized from Sn granules, and I2 (99.8%)),(CH3)2CHNH3I (synthesized from (CH3)2C(H)NH2 (99.5%) and HI)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnI2 (1116 mg, 3 mmol) was dissolved in solution, and flask was heated to boiling (~130 \\u00baC) via an oil bath. A bright yellow solution formed under magnetic stirring. Solid (CH3)2CHNH3I (1683 mg, 9 mmol) was added to the solution, and a pale-yellow precipitate formed within 5 minutes. The temperature was raised to 200\\u00ba C, and the precipitate turned red. The solution was cooled and precipitate changed back to yellow.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ac2a\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1315,\n        \"id\": 336,\n        \"compound_name\": \"Bis(butylammonium) methylammonium tin iodide\",\n        \"formula\": \"CH3(CH2)3(NH3)2(CH3NH3)Sn2I7\",\n        \"group\": \"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Sn2I7, Tin iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnCl2\\u00b72H2O (98%), CH3NH3Cl (98%), CH3(CH2)3NH2\",\n        \"synthesis_product\": \"cherry-red rectangular plates\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnCl2\\u20222H2O powder (2256 mg, 10 mmol) was dissolved in a solution of 57% (w/w) aqueous HI solution (20 mL, 152 mmol) and 50% aqueous H3PO2 (3.4 mL, 31 mmol) by boiling the solution and constantly stirring. This formed a bright yellow solution. Solid CH3(CH2)3NH2 (694 \\u03bcL, 7 mmol) was neutralized with 57% (w/w) HI (5 mL38 mmol) via an ice bath. This resulted in a clear pale-yellow solution. CH3(CH2)3NH3I solution was added to SnI2 solution and produced a black precipitate. After the solution was boiled, stirring stopped, the solution cooled, and crystals formed for 2 hours.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"SC-XRD was performed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5), operating at 50 kV and 40 mA. Integration/numerical absorption corrections were executed with X-AREA, X-RED, and X-SHAPE programs.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ama2\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1316,\n        \"id\": 336,\n        \"compound_name\": \"Bis(butylammonium) methylammonium tin iodide\",\n        \"formula\": \"CH3(CH2)3(NH3)2(CH3NH3)Sn2I7\",\n        \"group\": \"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Sn2I7, Tin iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnCl2\\u00b72H2O (98%), CH3NH3Cl (98%), CH3(CH2)3NH2\",\n        \"synthesis_product\": \"cherry-red rectangular plates\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnCl2\\u20222H2O powder (2256 mg, 10 mmol) was dissolved in a solution of 57% (w/w) aqueous HI solution (20 mL, 152 mmol) and 50% aqueous H3PO2 (3.4 mL, 31 mmol) by boiling the solution and constantly stirring. This formed a bright yellow solution. Solid CH3(CH2)3NH2 (694 \\u03bcL, 7 mmol) was neutralized with 57% (w/w) HI (5 mL38 mmol) via an ice bath. This resulted in a clear pale-yellow solution. CH3(CH2)3NH3I solution was added to SnI2 solution and produced a black precipitate. After the solution was boiled, stirring stopped, the solution cooled, and crystals formed for 2 hours.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference. Generated reflectance v. wavelength data was used to estimate the band gap. The Kubelka-Munk equation \\u03b1/S = (1-R)^{2}/(2R) was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ama2\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1317,\n        \"id\": 336,\n        \"compound_name\": \"Bis(butylammonium) methylammonium tin iodide\",\n        \"formula\": \"CH3(CH2)3(NH3)2(CH3NH3)Sn2I7\",\n        \"group\": \"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Sn2I7, Tin iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ama2\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b02764\",\n        \"dataset_ID\": 1318,\n        \"id\": 336,\n        \"compound_name\": \"Bis(butylammonium) methylammonium tin iodide\",\n        \"formula\": \"CH3(CH2)3(NH3)2(CH3NH3)Sn2I7\",\n        \"group\": \"(BA)2(MA)Sn2I7, bis(butylaminium) methanaminium septaiodo distannate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Sn2I7, Tin iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structure\\u2212Band Gap Relationships in Hexagonal Polytypes and Low- Dimensional Structures of Hybrid Tin Iodide Perovskites\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"73\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"distilled HI (aqueous 99.95%), H3PO2 (50% aqueous), SnCl2\\u00b72H2O (98%), CH3NH3Cl (98%), CH3(CH2)3NH2\",\n        \"synthesis_product\": \"cherry-red rectangular plates\",\n        \"synthesis_description\": \"Two-necked flask was charged with aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (1.7 mL, 9.14 M). Nitrogen  was passed through the liquid to degass the solution. SnCl2\\u20222H2O powder (2256 mg, 10 mmol) was dissolved in a solution of 57% (w/w) aqueous HI solution (20 mL, 152 mmol) and 50% aqueous H3PO2 (3.4 mL, 31 mmol) by boiling the solution and constantly stirring. This formed a bright yellow solution. Solid CH3(CH2)3NH2 (694 \\u03bcL, 7 mmol) was neutralized with 57% (w/w) HI (5 mL38 mmol) via an ice bath. This resulted in a clear pale-yellow solution. CH3(CH2)3NH3I solution was added to SnI2 solution and produced a black precipitate. After the solution was boiled, stirring stopped, the solution cooled, and crystals formed for 2 hours.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"Diffuse-reflectance measurements were performed and collected at room temperature. A Shimadzu UV-3600 PC double-beam and double monochromator spectrophotometer (operating between 200 to 2500 nm) was used.BaSO4 was used as a nonabsorbing reflectance reference.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ama2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.nanolett.5b02082\",\n        \"dataset_ID\": 1320,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Electroluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Growth and Anion Exchange Conversion of CH3NH3PbX3 Nanorod Arrays for Light-Emitting Diodes\",\n        \"journal\": \"Nano Letters\",\n        \"vol\": \"15\",\n        \"pages_start\": \"5519\",\n        \"pages_end\": \"5524\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"CH3NH3Br (5- 9 mg/mL), Anhydrous isopropanol (4 mL), PEDOT:PSS, Aldrich ( 10 \\u00b5L)\",\n        \"synthesis_product\": \"CH3NH3PbBr3 Nanorod Arrays\",\n        \"synthesis_description\": \"ITO substrated was coated with PEDOT: PSS (Clevios) at 3000 rpm for 40 seconds and followed by heating at 150 \\u00b0C for 15 minutes. Using a methanolic solution, ITO substrated was coated with 10 \\u00b5L of lead acetate trihydrate (Aldrich). The chips formed were heated at  65\\u00b0C and stored in a glove box filled with nitrogen gas. Then CH3NH3Br ( 5 mg/mL to 9 mg/mL ) was dissolved in n 4 mL of anhydrous\\r\\nisopropanol (Aldrich), which was mixed with ITO/PEDOT: PSS/lead acetate substrate. An orange film began to grow on the substrate and CH3NH3PbBr3 arrays were produced.\",\n        \"experimental_method\": \"UV-Vis spectrometer\",\n        \"experimental_description\": \"Chips of CH3NH3PbBr3 were placed into a vial, in which they were hooked to a cable tie and submerged into an oil bath at 140 to 150 \\u00b0C. The vial contained 0.1g of CH3NH3I which enabled direct contacts between the solutions. Partial anion exchange was achieved because of the separation of CH3NH3X and PbX2. The electroluminescence was observed were observed from the from hybrid perovskite nanocrystals blended with a thin polyimide dielectric polymer using a Shimadzu UV-3101 UV-Vis spectrometer equipped with an integrating sphere.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B618196A\",\n        \"dataset_ID\": 1322,\n        \"id\": 341,\n        \"compound_name\": \"Bis(cyclopropylammonium) lead iodide\",\n        \"formula\": \"(C3H5NH3)2PbI4\",\n        \"group\": \"Cyclopropylammonium lead iodide, bis(cyclopropylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C3NH8\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclopropylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead iodide series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"9\",\n        \"pages_start\": \"236\",\n        \"pages_end\": \"244\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C3H5NH2\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B618196A\",\n        \"dataset_ID\": 1323,\n        \"id\": 342,\n        \"compound_name\": \"Bis(cyclobutylammonium) lead iodide\",\n        \"formula\": \"(C4H7NH3)2PbI4\",\n        \"group\": \"Cyclobutylammonium lead iodide, bis(cyclobutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C4H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclobutylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead iodide series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"9\",\n        \"pages_start\": \"236\",\n        \"pages_end\": \"244\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C4H7NH2\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B618196A\",\n        \"dataset_ID\": 1324,\n        \"id\": 343,\n        \"compound_name\": \"Bis(cyclopentylammonium) lead iodide\",\n        \"formula\": \"(C5H9NH3)2PbI4\",\n        \"group\": \"Cyclopentylammonium lead iodide, bis(cyclopentylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5NH12\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclopentylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead iodide series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"9\",\n        \"pages_start\": \"236\",\n        \"pages_end\": \"244\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C5H9NH2\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B618196A\",\n        \"dataset_ID\": 1325,\n        \"id\": 411,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead iodide\",\n        \"formula\": \"(C6H14N)2PbI4\",\n        \"group\": \"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead iodide series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"9\",\n        \"pages_start\": \"236\",\n        \"pages_end\": \"244\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C6H11NH2\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B618196A\",\n        \"dataset_ID\": 1326,\n        \"id\": 345,\n        \"compound_name\": \"Tris(cycloheptylammonium) lead iodide\",\n        \"formula\": \"(C7H13NH3)3PbI4\",\n        \"group\": \"Cycloheptylammonium lead iodide, tris(cycloheptylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C7H13NH3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"tris(cycloheptylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead iodide series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"9\",\n        \"pages_start\": \"236\",\n        \"pages_end\": \"244\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C7H13NH2\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B618196A\",\n        \"dataset_ID\": 1327,\n        \"id\": 346,\n        \"compound_name\": \"Cyclooctylammonium lead iodide\",\n        \"formula\": \"(C8H15NH3)PbI4\",\n        \"group\": \"Cyclooctylammonium lead iodide, cyclooctylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H15NH3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"cyclooctylaminium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead iodide series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"9\",\n        \"pages_start\": \"236\",\n        \"pages_end\": \"244\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbI2, HI, C8H15NH2\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2 was dissolved in HI and then the organic cyclic amine was added. A precipitate was immediately formed and was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to carry out the data reduction and the XPREP program was used to carry out face indexed absorption corrections. The structure was solved with the SHELXS-97 program and was refined with the SHELXL-97 program by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1328,\n        \"id\": 347,\n        \"compound_name\": \"Bis(2-chloroethylammonium) lead iodide\",\n        \"formula\": \"(Cl(CH2)2NH3)2PbI4\",\n        \"group\": \"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NCl\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-chloroethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker-Nonius KAPPA-CDD diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. The Shelxl97 package was used to both solve and refine the structures.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbnm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1329,\n        \"id\": 296,\n        \"compound_name\": \"Bis(2-bromoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2Br2PbI4\",\n        \"group\": \"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NBr\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-bromoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker-Nonius KAPPA-CDD diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. The Shelxl97 package was used to both solve and refine the structures.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Phase 1: Space Group C2/c\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1330,\n        \"id\": 291,\n        \"compound_name\": \"Bis(2-iodoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2PbI6\",\n        \"group\": \"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-iodoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, I(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker-Nonius KAPPA-CDD diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. The Shelxl97 package was used to both solve and refine the structures.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1331,\n        \"id\": 347,\n        \"compound_name\": \"Bis(2-chloroethylammonium) lead iodide\",\n        \"formula\": \"(Cl(CH2)2NH3)2PbI4\",\n        \"group\": \"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NCl\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-chloroethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1332\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1332,\n        \"id\": 347,\n        \"compound_name\": \"Bis(2-chloroethylammonium) lead iodide\",\n        \"formula\": \"(Cl(CH2)2NH3)2PbI4\",\n        \"group\": \"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NCl\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-chloroethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1331\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1333,\n        \"id\": 296,\n        \"compound_name\": \"Bis(2-bromoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2Br2PbI4\",\n        \"group\": \"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NBr\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-bromoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1334\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbnm\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1334,\n        \"id\": 296,\n        \"compound_name\": \"Bis(2-bromoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2Br2PbI4\",\n        \"group\": \"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NBr\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-bromoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1333\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Thin film on glass substrate\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours. Thin films of the samples were prepared via spin-coating solutions of dissolved crystals in acetonitrile.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1335,\n        \"id\": 291,\n        \"compound_name\": \"Bis(2-iodoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2PbI6\",\n        \"group\": \"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-iodoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1336\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, I(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1336,\n        \"id\": 291,\n        \"compound_name\": \"Bis(2-iodoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2PbI6\",\n        \"group\": \"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-iodoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1335\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, I(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Lambda 19 Perkin-Elmer spectrometer using a Specac variable temperature cell P/N 21525 was used to directly measure the absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1337,\n        \"id\": 347,\n        \"compound_name\": \"Bis(2-chloroethylammonium) lead iodide\",\n        \"formula\": \"(Cl(CH2)2NH3)2PbI4\",\n        \"group\": \"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NCl\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-chloroethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"mg\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Cl(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Cl-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"A TGA-2050 Instruments System was used to perform the dynamic thermogravimetric analysis measurements under a nitrogen atmosphere. The temperature was increased at 10 degrees Celsius per minute over the range 25 to 900 degrees Celsius.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1338,\n        \"id\": 296,\n        \"compound_name\": \"Bis(2-bromoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2Br2PbI4\",\n        \"group\": \"2-bromoethylammonium lead iodide, (Br(CH2)2NH3)2PbI4, bis(2-bromoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NBr\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-bromoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, Br(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, Br-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"A TGA-2050 Instruments System was used to perform the dynamic thermogravimetric analysis measurements under a nitrogen atmosphere. The temperature was increased at 10 degrees Celsius per minute over the range 25 to 900 degrees Celsius.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1339,\n        \"id\": 291,\n        \"compound_name\": \"Bis(2-iodoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2PbI6\",\n        \"group\": \"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-iodoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"mg\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"Acetonitrile, HI, I(CH2)2NH2, PbI2\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"In 6:2:1 molar ratio HI, I-(CH2)2-NH2, and PbI2 were added to an acetonitrile solution. It was stirred for a short time at room temperature, forming a clear and yellow solution. It was then held at room temperature and allowed to evaporate, leaving behind crystals of the perovskite after a few hours.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"A TGA-2050 Instruments System was used to perform the dynamic thermogravimetric analysis measurements under a nitrogen atmosphere. The temperature was increased at 10 degrees Celsius per minute over the range 25 to 900 degrees Celsius.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1340,\n        \"id\": 347,\n        \"compound_name\": \"Bis(2-chloroethylammonium) lead iodide\",\n        \"formula\": \"(Cl(CH2)2NH3)2PbI4\",\n        \"group\": \"2-chloroethylammonium lead iodide, bis(2-chloroethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NCl\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-chloroethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP Package, WIEN2K Package\",\n        \"level_of_theory\": \"DFT, FLAPW method\",\n        \"xc_functional\": \"PBE96\",\n        \"k_point_grid\": \"6x6x4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm062380e\",\n        \"dataset_ID\": 1341,\n        \"id\": 291,\n        \"compound_name\": \"Bis(2-iodoethylammonium) lead iodide\",\n        \"formula\": \"C4H14N2PbI6\",\n        \"group\": \"2-iodoethylammonium lead iodide, (I(CH2)2NH3)2PbI4, bis(2-iodoethylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C2H7NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-iodoethylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"VASP Package, WIEN2K Package\",\n        \"level_of_theory\": \"DFT, FLAPW method\",\n        \"xc_functional\": \"PBE96\",\n        \"k_point_grid\": \"8x4x2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reduced Band Gap Hybrid Perovskites Resulting from Combined Hydrogen and Halogen Bonding at the Organic\\u2212Inorganic Interface\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"19\",\n        \"pages_start\": \"600\",\n        \"pages_end\": \"607\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsaem.9b00419\",\n        \"dataset_ID\": 1343,\n        \"id\": 348,\n        \"compound_name\": \"Azetidinium lead bromide\",\n        \"formula\": \"C3H8Br3NPb\",\n        \"group\": \"AzPbBr3, methanaminium tribromoplumbate(II)\",\n        \"organic\": \"C3H8N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Azetidinium lead bromide\",\n        \"last_update\": \"2022-08-03\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stable 6H Organic\\u2013Inorganic Hybrid Lead Perovskite and Competitive Formation of 6H and 3C Perovskite Structure with Mixed A Cations\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"8\",\n        \"pages_start\": \"5427\",\n        \"pages_end\": \"5437\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AzBr (synthesized from AzCl (0.94 g, 10 mmol, 1 equiv.) and NaBr (2.05g, 20 mmol, 2 equiv.)), PbBr2, DMF/DMSO (4:1), Acetonitrile\",\n        \"synthesis_product\": \"Pale yellow needle-like crystals\",\n        \"synthesis_description\": \"AzPbBr3 was prepared by mixing AzBr with PbBr2 in DMF/DMSO (4:1) solution by stirring for 2 h. Acetonitrile was added slowly into the solution and left to stand for 10 min before filtration. The resulting powder was filtered and washed.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"An analysis of the single crystals of AzPbBr3 was performed using TGA via an Integrated Thermo-gravimetric Analyzer (TGA/DTA3600). The data for AzPbBr3 via a thermogravimetric analysis was obtained from room temperature to 700 \\u00b0C.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P6(3)/mmc\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1345,\n        \"id\": 349,\n        \"compound_name\": \"Bis(cyclopropylammonium) lead bromide\",\n        \"formula\": \"(C3H5NH3)2PbBr4\",\n        \"group\": \"Cyclopropylammonium lead bromide, bis(cyclopropylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C3H5NH3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclopropylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, C3H5NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1346,\n        \"id\": 350,\n        \"compound_name\": \"Bis(cyclobutylammonium) lead bromide\",\n        \"formula\": \"(C4H7NH3)2PbBr4\",\n        \"group\": \"Cyclobutylammonium lead bromide, bis(cyclobutylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C4H7NH3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclobutylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, C4H7NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1347,\n        \"id\": 351,\n        \"compound_name\": \"Bis(cyclopentylammonium) lead bromide\",\n        \"formula\": \"(C5H9NH3)2PbBr4\",\n        \"group\": \"Cyclopentylammonium lead bromide, bis(cyclopentylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C5H9NH3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclopentylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, C5H9NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1348,\n        \"id\": 410,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead bromide\",\n        \"formula\": \"(C6H14N)2PbBr4\",\n        \"group\": \"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, C6H11NH2\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1349,\n        \"id\": 353,\n        \"compound_name\": \"Tris(cycloheptylammonium) lead bromide\",\n        \"formula\": \"(C7H13NH3)3PbBr4\",\n        \"group\": \"Cycloheptylammonium lead bromide, tris(cycloheptylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C7H13NH3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"tris(cycloheptylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, C7H13NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1350,\n        \"id\": 354,\n        \"compound_name\": \"Cyclooctylammonium lead bromide\",\n        \"formula\": \"(C8H15NH3)PbBr4\",\n        \"group\": \"Cyclooctylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C8H15NH3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"cyclooctylaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, C8H15NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbBr2 was dissolved in an HBr solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1351,\n        \"id\": 355,\n        \"compound_name\": \"Bis(cyclopropylammonium) lead chloride\",\n        \"formula\": \"(C3H5NH3)2PbCl4\",\n        \"group\": \"Cyclopropylammonium lead chloride, bis(cyclopropylaminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C3H5NH3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(cyclopropylaminium) lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, C3H5NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1352,\n        \"id\": 356,\n        \"compound_name\": \"Bis(cyclobutylammonium) lead chloride\",\n        \"formula\": \"(C4H7NH3)2PbCl4\",\n        \"group\": \"Cyclobutylammonium lead chloride, bis(cyclobutylaminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C4H7NH3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(cyclobutylaminium) lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, C4H7NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1353,\n        \"id\": 357,\n        \"compound_name\": \"Bis(cyclopentylammonium) lead chloride\",\n        \"formula\": \"(C5H9NH3)2PbCl4\",\n        \"group\": \"Cyclopentylammonium lead chloride, bis(cyclopentylaminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C5H9NH3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(cyclopentylaminium) lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, C5H9NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1354,\n        \"id\": 358,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead chloride\",\n        \"formula\": \"(C6H11NH3)2PbCl4\",\n        \"group\": \"Cyclohexylammonium lead chloride, bis(cyclohexylaminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C6H11NH3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, C6H11NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1355,\n        \"id\": 359,\n        \"compound_name\": \"Tris(cycloheptylammonium) lead chloride\",\n        \"formula\": \"(C7H13NH3)3PbCl4\",\n        \"group\": \"Cycloheptylammonium lead chloride, tris(cycloheptylaminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C7H13NH3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"tris(cycloheptylaminium) lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, C7H13NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B819455F\",\n        \"dataset_ID\": 1356,\n        \"id\": 360,\n        \"compound_name\": \"Cyclooctylammonium lead chloride\",\n        \"formula\": \"(C8H15NH3)PbCl4\",\n        \"group\": \"Cyclooctylammonium tetrachloroplumbate(II)\",\n        \"organic\": \"C8H15NH3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"cyclooctylaminium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Inorganic\\u2013organic hybrid materials incorporating primary cyclic ammonium cations: The lead bromide and chloride series\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"11\",\n        \"pages_start\": \"1549\",\n        \"pages_end\": \"1562\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"PbCl2, HCl, C8H15NH2\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"PbCl2 was dissolved in an HCl solution. Then, the cyclic amine was added and immediately resulted in the precipitation of a solid, which was re-dissolved by refluxing for 1-12 hours. The solution was then cooled slowly to room temperature, causing crystals to precipitate.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker SMART 1K CCD area detector diffractometer using Mo Kalpha radiation was used to collect the SCXRD data. Omega-scans of width 0.3 degrees were used. The SAINT+ program, version 6.02, was used to perform data reduction and the XPREP program was used to perform face indexed absorption corrections. The SHELXS-97 program was used for solving the structure, and the SHELXL-97 program was used to refine it by full matrix least-squares minimization.\",\n        \"physical_property\": \"173.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm060714u\",\n        \"dataset_ID\": 1358,\n        \"id\": 361,\n        \"compound_name\": \"N-(3-aminopropyl)imidazole lead bromide\",\n        \"formula\": \"(C3H4N2(CH2)3NH3)PbBr4\",\n        \"group\": \"(API)PbBr4, N-(3-aminopropyl)imidazole lead bromide, N-(3-aminopropyl)imidazole tetrabromoplumbate(II)\",\n        \"organic\": \"C6H13N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-(3-aminopropyl)imidazole lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Novel \\u2329110\\u232a-Oriented Organic-Inorganic Perovskite Compound Stabilized by N-(3-Aminopropyl)imidazole with Improved Optical Properties\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"18\",\n        \"pages_start\": \"3463\",\n        \"pages_end\": \"3469\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"N-(3-aminopropyl)imidazole (API, 98%, Aldrich), PbBr2 (99.999%, Aldrich), HBr (\\u226540%, Beijing Chemical Industry Co., Ltd.)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"A solution of PbBr2, API, and HBr was heated to 70 degrees Celsius and then cooled at 3 degrees per hour until reaching room temperature. This was performed in a nitrogen atmosphere and the crystals precipitated upon cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku RAXIS-RAPID image plate diffractometer was used to measure SCXRD. The w-scan technique was employed, and Mo Kalpha radiation was used. The SHELXS-97 program was used to solve the structure and the SHELXL-97 program was used to refine it via the full-matrix least-squares techniques.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm060714u\",\n        \"dataset_ID\": 1359,\n        \"id\": 361,\n        \"compound_name\": \"N-(3-aminopropyl)imidazole lead bromide\",\n        \"formula\": \"(C3H4N2(CH2)3NH3)PbBr4\",\n        \"group\": \"(API)PbBr4, N-(3-aminopropyl)imidazole lead bromide, N-(3-aminopropyl)imidazole tetrabromoplumbate(II)\",\n        \"organic\": \"C6H13N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-(3-aminopropyl)imidazole lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Novel \\u2329110\\u232a-Oriented Organic-Inorganic Perovskite Compound Stabilized by N-(3-Aminopropyl)imidazole with Improved Optical Properties\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"18\",\n        \"pages_start\": \"3463\",\n        \"pages_end\": \"3469\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"N-(3-aminopropyl)imidazole (API, 98%, Aldrich), PbBr2 (99.999%, Aldrich), HBr (\\u226540%, Beijing Chemical Industry Co., Ltd.), DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"A solution of PbBr2, API, and HBr was heated to 70 degrees Celsius and then cooled at 3 degrees per hour until reaching room temperature. This was performed in a nitrogen atmosphere and the crystals precipitated upon cooling. Thin films were prepared via spin-coating. The crystals were dissolved into a DMF solution that was spin-coated onto a quartz substrate. The spinning cycle parameters were a spin rate of 1500 for 50 seconds and was followed by annealing the sample at 100 degrees Celsius for 20 minutes.\",\n        \"experimental_method\": \"Photoluminescence Excitation Spectroscopy\",\n        \"experimental_description\": \"A Hitachi F-4500 spectrofluorimeter using a 150 W xenon lamp was used to measure the photoluminescence excitation and emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm060714u\",\n        \"dataset_ID\": 1360,\n        \"id\": 361,\n        \"compound_name\": \"N-(3-aminopropyl)imidazole lead bromide\",\n        \"formula\": \"(C3H4N2(CH2)3NH3)PbBr4\",\n        \"group\": \"(API)PbBr4, N-(3-aminopropyl)imidazole lead bromide, N-(3-aminopropyl)imidazole tetrabromoplumbate(II)\",\n        \"organic\": \"C6H13N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-(3-aminopropyl)imidazole lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Novel \\u2329110\\u232a-Oriented Organic-Inorganic Perovskite Compound Stabilized by N-(3-Aminopropyl)imidazole with Improved Optical Properties\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"18\",\n        \"pages_start\": \"3463\",\n        \"pages_end\": \"3469\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"N-(3-aminopropyl)imidazole (API, 98%, Aldrich), PbBr2 (99.999%, Aldrich), HBr (\\u226540%, Beijing Chemical Industry Co., Ltd.), DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"A solution of PbBr2, API, and HBr was heated to 70 degrees Celsius and then cooled at 3 degrees per hour until reaching room temperature. This was performed in a nitrogen atmosphere and the crystals precipitated upon cooling. Thin films were prepared via spin-coating. The crystals were dissolved into a DMF solution that was spin-coated onto a quartz substrate. The spinning cycle parameters were a spin rate of 1500 for 50 seconds and was followed by annealing the sample at 100 degrees Celsius for 20 minutes.\",\n        \"experimental_method\": \"Photoluminescence Excitation Spectroscopy\",\n        \"experimental_description\": \"A Hitachi F-4500 spectrofluorimeter using a 150 W xenon lamp was used to measure the photoluminescence excitation and emission spectra. Excitation wavelength of 360 nm was used for the emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acscentsci.6b00055\",\n        \"dataset_ID\": 1362,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"High-Pressure Single-Crystal Structures of 3D Lead-Halide Hybrid Perovskites and Pressure Effects on their Electronic and Optical Properties\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"4\",\n        \"pages_start\": \"201\",\n        \"pages_end\": \"209\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Frames were collected using a Bruker D85 diffractometer equipped with a Photon 100 CMOS detector. Synchrotron X-rays at Beamline 11.3.1 at the ALS, LBNL were monochromated using silicon(111).\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fmmm\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1363,\n        \"id\": 363,\n        \"compound_name\": \"Bis(pentylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)Pb2I7\",\n        \"group\": \"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 \\u03bcL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Single crystal X-Ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb=0.71073 \\u00c5) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1364,\n        \"id\": 363,\n        \"compound_name\": \"Bis(pentylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)Pb2I7\",\n        \"group\": \"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 \\u03bcL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1365,\n        \"id\": 363,\n        \"compound_name\": \"Bis(pentylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)Pb2I7\",\n        \"group\": \"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 \\u03bcL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1366,\n        \"id\": 363,\n        \"compound_name\": \"Bis(pentylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)Pb2I7\",\n        \"group\": \"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 \\u03bcL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1367,\n        \"id\": 364,\n        \"compound_name\": \"Bis(pentylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)2Pb3I10\",\n        \"group\": \"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 \\u03bcL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Single crystal X-Ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb=0.71073 \\u00c5) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1368,\n        \"id\": 364,\n        \"compound_name\": \"Bis(pentylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)2Pb3I10\",\n        \"group\": \"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 \\u03bcL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1370,\n        \"id\": 363,\n        \"compound_name\": \"Bis(pentylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)Pb2I7\",\n        \"group\": \"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 \\u03bcL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1371,\n        \"id\": 364,\n        \"compound_name\": \"Bis(pentylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)2Pb3I10\",\n        \"group\": \"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 \\u03bcL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1372,\n        \"id\": 364,\n        \"compound_name\": \"Bis(pentylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)2Pb3I10\",\n        \"group\": \"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 \\u03bcL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1374,\n        \"id\": 365,\n        \"compound_name\": \"Bis(pentylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)3Pb4I13\",\n        \"group\": \"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Single crystal X-Ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb=0.71073 \\u00c5) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1375,\n        \"id\": 363,\n        \"compound_name\": \"Bis(pentylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)Pb2I7\",\n        \"group\": \"(PA)2(MA)Pb2I7, bis(pentylaminium) methanaminium septaiododiplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1376,\n        \"id\": 365,\n        \"compound_name\": \"Bis(pentylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)3Pb4I13\",\n        \"group\": \"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1377,\n        \"id\": 365,\n        \"compound_name\": \"Bis(pentylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)3Pb4I13\",\n        \"group\": \"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1378,\n        \"id\": 365,\n        \"compound_name\": \"Bis(pentylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)3Pb4I13\",\n        \"group\": \"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1379,\n        \"id\": 365,\n        \"compound_name\": \"Bis(pentylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)3Pb4I13\",\n        \"group\": \"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 911 \\u03bcL (6.9 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"453.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1380,\n        \"id\": 364,\n        \"compound_name\": \"Bis(pentylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)2Pb3I10\",\n        \"group\": \"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask. The solution was heated and stirred constantly. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine was added to 50% aqueous H3PO2 (2 mL) and solution reacted slowly. The solution was cooled on a hot plate and eventually cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1381,\n        \"id\": 366,\n        \"compound_name\": \"Bis(pentylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)4Pb5I16\",\n        \"group\": \"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Single crystal X-Ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb=0.71073 \\u00c5) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1382,\n        \"id\": 366,\n        \"compound_name\": \"Bis(pentylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)4Pb5I16\",\n        \"group\": \"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1383,\n        \"id\": 366,\n        \"compound_name\": \"Bis(pentylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)4Pb5I16\",\n        \"group\": \"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1384,\n        \"id\": 364,\n        \"compound_name\": \"Bis(pentylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)2Pb3I10\",\n        \"group\": \"(PA)2(MA)2Pb3I10, bis(pentylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 383 \\u03bcL (3.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1385,\n        \"id\": 366,\n        \"compound_name\": \"Bis(pentylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)4Pb5I16\",\n        \"group\": \"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (540 mg, 8 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.3 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1386,\n        \"id\": 365,\n        \"compound_name\": \"Bis(pentylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)3Pb4I13\",\n        \"group\": \"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1387,\n        \"id\": 367,\n        \"compound_name\": \"Bis(hexylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)Pb2I7\",\n        \"group\": \"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 \\u03bcL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Single crystal X-Ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb=0.71073 \\u00c5) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1388,\n        \"id\": 365,\n        \"compound_name\": \"Bis(pentylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)3Pb4I13\",\n        \"group\": \"(PA)2(MA)3Pb4I13, bis(pentylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1389,\n        \"id\": 367,\n        \"compound_name\": \"Bis(hexylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)Pb2I7\",\n        \"group\": \"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 \\u03bcL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1390,\n        \"id\": 367,\n        \"compound_name\": \"Bis(hexylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)Pb2I7\",\n        \"group\": \"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 \\u03bcL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1391,\n        \"id\": 367,\n        \"compound_name\": \"Bis(hexylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)Pb2I7\",\n        \"group\": \"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 \\u03bcL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1392,\n        \"id\": 368,\n        \"compound_name\": \"Bis(hexylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)2Pb3I10\",\n        \"group\": \"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 \\u03bcL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Single crystal X-Ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb=0.71073 \\u00c5) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1393,\n        \"id\": 368,\n        \"compound_name\": \"Bis(hexylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)2Pb3I10\",\n        \"group\": \"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 \\u03bcL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1394,\n        \"id\": 366,\n        \"compound_name\": \"Bis(pentylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)4Pb5I16\",\n        \"group\": \"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask. The solution was heated and stirred constantly. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine was added to 50% aqueous H3PO2 (2 mL) and solution reacted slowly. The solution was cooled on a hot plate and eventually cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1395,\n        \"id\": 368,\n        \"compound_name\": \"Bis(hexylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)2Pb3I10\",\n        \"group\": \"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 \\u03bcL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1396,\n        \"id\": 368,\n        \"compound_name\": \"Bis(hexylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)2Pb3I10\",\n        \"group\": \"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 \\u03bcL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1397,\n        \"id\": 369,\n        \"compound_name\": \"Bis(hexylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)3Pb4I13\",\n        \"group\": \"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Single crystal X-Ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb=0.71073 \\u00c5) and MX Optics was used. All samples were collected at 293 K. Data was integrated and corrected for absorption with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1398,\n        \"id\": 366,\n        \"compound_name\": \"Bis(pentylammonium) tetrakis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2(MA)4Pb5I16\",\n        \"group\": \"(PA)2(MA)4Pb5I16, bis(pentylaminium) tetrakis(methanaminium) hexadecaiodo pentaplumbate(II)\",\n        \"organic\": \"C5NH14, CNH6\",\n        \"inorganic\": \"Pb5I16, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) tetrakis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"5\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask. The solution was heated and stirred constantly. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 232 \\u03bcL (2 mmol) of pentylamine was added to 50% aqueous H3PO2 (2 mL) and solution reacted slowly. The solution was cooled on a hot plate and eventually cooled to room temperature. After three hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1399,\n        \"id\": 367,\n        \"compound_name\": \"Bis(hexylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)Pb2I7\",\n        \"group\": \"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 \\u03bcL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1400,\n        \"id\": 367,\n        \"compound_name\": \"Bis(hexylammonium) methylammonium lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)Pb2I7\",\n        \"group\": \"(HA)2(MA)Pb2I7, bis(hexylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"red plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (338 mg, 5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 580 \\u03bcL (4.39 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1401,\n        \"id\": 368,\n        \"compound_name\": \"Bis(hexylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)2Pb3I10\",\n        \"group\": \"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 \\u03bcL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1402,\n        \"id\": 368,\n        \"compound_name\": \"Bis(hexylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)2Pb3I10\",\n        \"group\": \"(HA)2(MA)2Pb3I10, bis(hexylaminium) bis(methanaminium) decaiodo triplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) bis(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"brown plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (450 mg, 6.67 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 250 \\u03bcL (1.89 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1403,\n        \"id\": 369,\n        \"compound_name\": \"Bis(hexylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)3Pb4I13\",\n        \"group\": \"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1404,\n        \"id\": 369,\n        \"compound_name\": \"Bis(hexylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)3Pb4I13\",\n        \"group\": \"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1405,\n        \"id\": 369,\n        \"compound_name\": \"Bis(hexylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)3Pb4I13\",\n        \"group\": \"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1406,\n        \"id\": 369,\n        \"compound_name\": \"Bis(hexylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)3Pb4I13\",\n        \"group\": \"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1407,\n        \"id\": 369,\n        \"compound_name\": \"Bis(hexylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2(MA)3Pb4I13\",\n        \"group\": \"(HA)2(MA)3Pb4I13, bis(hexylaminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C6NH16, CNH6\",\n        \"inorganic\": \"Pb4I13, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) tris(methanaminium) lead iodide\",\n        \"last_update\": \"2022-08-16\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), methylamine hydrochloride (\\u226598%), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. Solid methylamine hydrochloride (507 mg, 7.5 mmol, DRY) was added to the hot yellow solution, and a black powder precipitated. This dissolved under stirring and resulted in a bright yellow solution. 150 \\u03bcL (1.17 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature. After two hours, crystals were completely formed.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1408,\n        \"id\": 370,\n        \"compound_name\": \"Bis(pentylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2PbI4\",\n        \"group\": \"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 \\u03bcL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1409,\n        \"id\": 370,\n        \"compound_name\": \"Bis(pentylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2PbI4\",\n        \"group\": \"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 \\u03bcL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1410,\n        \"id\": 370,\n        \"compound_name\": \"Bis(pentylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2PbI4\",\n        \"group\": \"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 \\u03bcL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1411,\n        \"id\": 370,\n        \"compound_name\": \"Bis(pentylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2PbI4\",\n        \"group\": \"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 \\u03bcL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/a\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1412,\n        \"id\": 371,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2PbI4\",\n        \"group\": \"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 \\u03bcL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1413,\n        \"id\": 370,\n        \"compound_name\": \"Bis(pentylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)4NH3)2PbI4\",\n        \"group\": \"(PA)2PbI4, bis(pentylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(pentylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), pentylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1159 \\u03bcL (10 mmol) of pentylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/a\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1414,\n        \"id\": 371,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2PbI4\",\n        \"group\": \"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 \\u03bcL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R. Band gap energy was calculated based on the absorption edge and exciton peak of the optical absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1415,\n        \"id\": 371,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2PbI4\",\n        \"group\": \"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 \\u03bcL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1416,\n        \"id\": 371,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2PbI4\",\n        \"group\": \"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 \\u03bcL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600g/mm diffraction grating, with a diode continuous wave laser (473 nm, 25 mW) and a Synapse charge-coupled device camera. PL energy was calculated by the PL peak position of the optical emission spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b01327\",\n        \"dataset_ID\": 1417,\n        \"id\": 371,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"(CH3(CH2)5NH3)2PbI4\",\n        \"group\": \"(HA)2PbI4, bis(hexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Uniaxial Expansion of the 2D Ruddlesden\\u2212Popper Perovskite Family for Improved Environmental Stability\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"5518\",\n        \"pages_end\": \"5534\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) oxide (PbO, <10 \\u03bcm, ReagentPlus\\u00ae, \\u226599.9% trace metals basis ), HI (57 wt. % in H2O), hexylamine 99%, H3PO2 (50 wt. % in H2O)\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in 57% w/w aqueous HI solution (16 mL) in a 50 mL glass flask by heating to boiling under stirring. A bright yellow solution resulted. 1000 \\u03bcL (7.52 mmol) of hexylamine in 50% aqueous H3PO2 (2 mL) was slowly added. The solution was slowly cooled to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Optical diffuse-reflectance measurements were conducted at room temperature. A Shimadzu UV-2600 PC double-beam, double-monochromator spectrophotometer was operating from 200 to 2500 nm. BaS4 was used as a non-absorbing reflectance reference. Reflectance v. wavelength data was collected and used to estimate the band gap by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1-R)^{2}/2R.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.jssc.2006.09.023\",\n        \"dataset_ID\": 1418,\n        \"id\": 69,\n        \"compound_name\": \"Histammonium lead bromide\",\n        \"formula\": \"C5H11N3PbBr4\",\n        \"group\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, structure and optical properties of new organic\\u2013inorganic haloplumbates complexes (C5H10N3)PbX4 (X=Br, Cl), (C2H2N4)PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"180\",\n        \"pages_start\": \"173\",\n        \"pages_end\": \"179\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbBr2 (99.99%), Histamine (98%), HBr (40%)\",\n        \"synthesis_product\": \"Pink crystals (yield: 40.3%)\",\n        \"synthesis_description\": \"Equimolar amounts of PbBr2 (0.367g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HBr by heating and refluxing at 90 \\u00b0C and then, the solution slowly cooled to room temperature in N2 atmosphere.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku RAXIS-RAPID image plate diffractometer employed the \\u03c9-scan technique and used Mo K\\u03b1 radiation (\\u03bb=0.71069 \\u00c5). Structures were solved via direct methods using SHELXS-97 and full-matrix least-squares techniques using SHELXL-97 implemented in WINGX.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.jssc.2006.09.023\",\n        \"dataset_ID\": 1419,\n        \"id\": 69,\n        \"compound_name\": \"Histammonium lead bromide\",\n        \"formula\": \"C5H11N3PbBr4\",\n        \"group\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, structure and optical properties of new organic\\u2013inorganic haloplumbates complexes (C5H10N3)PbX4 (X=Br, Cl), (C2H2N4)PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"180\",\n        \"pages_start\": \"173\",\n        \"pages_end\": \"179\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbBr2 (99.99%), Histamine (98%), HBr (40%), DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"For preparing the crystals, equimolar amounts of PbBr2 (0.367g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HBr by heating and refluxing at 90 \\u00b0C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 \\u00b0C for 20 minutes.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"A Hitachi F-4100 spectrofluorimeter was used to record the UV-Vis absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.jssc.2006.09.023\",\n        \"dataset_ID\": 1421,\n        \"id\": 69,\n        \"compound_name\": \"Histammonium lead bromide\",\n        \"formula\": \"C5H11N3PbBr4\",\n        \"group\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) tetrabromoplumbate(II), (HA)PbBr4, (HIS)PbBr4, (C5H11N3)PbBr4\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium) lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, structure and optical properties of new organic\\u2013inorganic haloplumbates complexes (C5H10N3)PbX4 (X=Br, Cl), (C2H2N4)PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"180\",\n        \"pages_start\": \"173\",\n        \"pages_end\": \"179\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbBr2 (99.99%), Histamine (98%), HBr (40%), DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"For preparing the crystals, equimolar amounts of PbBr2 (0.367g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HBr by heating and refluxing at 90 \\u00b0C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 \\u00b0C for 20 minutes.\",\n        \"experimental_method\": \"Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"A Hitachi F-4500 spectrofluorimeter was used for emission spectra. A 150 W xenon lamp was used as the excitation source.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.jssc.2006.09.023\",\n        \"dataset_ID\": 1422,\n        \"id\": 372,\n        \"compound_name\": \"Histammonium lead chloride\",\n        \"formula\": \"(C5H11N3)PbCl4\",\n        \"group\": \"(HIS)PbCl4(HA)PbCl4, Histammonium lead chloride, 4-(2-ethanaminium)-1H-imidazol-3-ium tetrachloroplumbate\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, structure and optical properties of new organic\\u2013inorganic haloplumbates complexes (C5H10N3)PbX4 (X=Br, Cl), (C2H2N4)PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"180\",\n        \"pages_start\": \"173\",\n        \"pages_end\": \"179\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"PbCl2 (99.99%), Histamine (98%), HCl (36%), DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"For preparing the crystals, equimolar amounts of PbCl2 (0.278g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HCl by heating and refluxing at 90 \\u00b0C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 \\u00b0C for 20 minutes.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"A Hitachi F-4100 spectrofluorimeter was used to measure the UV-Vis absorption spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.jssc.2006.09.023\",\n        \"dataset_ID\": 1423,\n        \"id\": 372,\n        \"compound_name\": \"Histammonium lead chloride\",\n        \"formula\": \"(C5H11N3)PbCl4\",\n        \"group\": \"(HIS)PbCl4(HA)PbCl4, Histammonium lead chloride, 4-(2-ethanaminium)-1H-imidazol-3-ium tetrachloroplumbate\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis, structure and optical properties of new organic\\u2013inorganic haloplumbates complexes (C5H10N3)PbX4 (X=Br, Cl), (C2H2N4)PbBr3\",\n        \"journal\": \"Journal of Solid State Chemistry\",\n        \"vol\": \"180\",\n        \"pages_start\": \"173\",\n        \"pages_end\": \"179\",\n        \"year\": \"2007\",\n        \"synthesis_starting_materials\": \"bCl2 (99.99%), Histamine (98%), HCl (36%), DMF\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"For preparing the crystals, equimolar amounts of PbCl2 (0.278g, 0.1 mmol) and histamine (0.113 g 0.1 mmol) were mixed in 10mL HCl by heating and refluxing at 90 \\u00b0C and then, the solution slowly cooled to room temperature in N2 atmosphere. 10 mg of the obtained single crystals were dissolved into 1.5 mL dried DMF solution and then the solution was coated onto a quartz substrate. The spin cycle spent 1 s accelerating to 1200 rmp and then stayed at that rotation speed for 50 s. The substrate was then heated to 100 \\u00b0C for 20 minutes.\",\n        \"experimental_method\": \"Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"A Hitachi F-4500 spectrofluorimeter was used for emission spectra. A 150 W xenon lamp was used as the excitation source.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay0571\",\n        \"dataset_ID\": 1424,\n        \"id\": 216,\n        \"compound_name\": \"bismethylbenzylammonium lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"(MBA)2PbI4, \\u0152\\u00b1-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bismethylbenzylaminium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"Chiral 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Chiral-induced spin Selectivity (CISS)\",\n        \"primary_unit\": \"nA\",\n        \"secondary_name\": \"bias\",\n        \"secondary_unit\": \"V\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Spin-dependent charge transport through 2D chiral hybrid lead-iodide perovskites\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"5\",\n        \"pages_start\": \"eaay0571\",\n        \"pages_end\": \"eaay0571\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"DMF, lead oxide (PbO, 99.999%), (R)-(+)-\\u03b1-methylbenzylamine (R-MBA, 98%, ee 96%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",\n        \"synthesis_product\": \"Thin film on ITO substrate\",\n        \"synthesis_description\": \"200 mg of PbO (0.897 mmol), 200 \\u03bcl (1.57 mmol) of R-MBA were dissolved in 6 ml of HI by heating at 90\\u00b0C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1\\u00b0C/hour. The obtained crystals were filtered and washed with diethyl ether. The crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto ITO substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100\\u00b0C for 10 min.\",\n        \"experimental_method\": \"Magnetic conductive-probe atomic force microscopy\",\n        \"experimental_description\": \"A Veeco D5000 AFM system in an Ar-filled glovebox with a NanoScope V controller was used to perform the conductive atomic force microscopy. A Bruker MESP-V2 tip was used. The Co-Cr coated tips were pre-magnetized by a strong permanent magnet for 30 minutes and immediately following were used to scan. I-V curves were generated by increasing the bias voltage from -2 to +2 Volts, and a scan rate of 0.5 Hz in contact mode was used. More than 100 I-V curves were taken in different locations for each sample.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Tip Up\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.aay0571\",\n        \"dataset_ID\": 1425,\n        \"id\": 216,\n        \"compound_name\": \"bismethylbenzylammonium lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"(MBA)2PbI4, \\u0152\\u00b1-methylbenzylammonium lead, (C6H5CH(CH3)NH3)2PbI4 iodide, 1-phenylethylammonium lead iodide, bismethylbenzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bismethylbenzylaminium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"Chiral 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Chiral-induced spin Selectivity (CISS)\",\n        \"primary_unit\": \"nA\",\n        \"secondary_name\": \"bias\",\n        \"secondary_unit\": \"V\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Spin-dependent charge transport through 2D chiral hybrid lead-iodide perovskites\",\n        \"journal\": \"Science Advances\",\n        \"vol\": \"5\",\n        \"pages_start\": \"eaay0571\",\n        \"pages_end\": \"eaay0571\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"DMF, lead oxide (PbO, 99.999%), (S)-(\\u2212)-\\u03b1-methylbenzylamine (S-MBA, 98%, ee 98%), 57% aqueous hydriodic acid (HI) solution (99.95%, distilled, stabilized by H3PO2)\",\n        \"synthesis_product\": \"Thin film on ITO substrate\",\n        \"synthesis_description\": \"200 mg of PbO (0.897 mmol), 200 \\u03bcl (1.57 mmol) of S-MBA were dissolved in 6 ml of HI by heating at 90\\u00b0C in an oil bath. The solution was slowly cooled to room temperature with a cooling rate of 1\\u00b0C/hour. The obtained crystals were filtered and washed with diethyl ether. The crystals were dissolved in DMF. Thin films were prepared by spin-coating the solution onto ITO substrates at a spin rate of 4000 rpm for 30 s. They were then annealed at 100\\u00b0C for 10 min.\",\n        \"experimental_method\": \"Magnetic conductive-probe atomic force microscopy\",\n        \"experimental_description\": \"A Veeco D5000 AFM system in an Ar-filled glovebox with a NanoScope V controller was used to perform the conductive atomic force microscopy. A Bruker MESP-V2 tip was used. The Co-Cr coated tips were pre-magnetized by a strong permanent magnet for 30 minutes and immediately following were used to scan. I-V curves were generated by increasing the bias voltage from -2 to +2 Volts, and a scan rate of 0.5 Hz in contact mode was used. More than 100 I-V curves were taken in different locations for each sample.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Tip Up\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.nanolett.5b02082\",\n        \"dataset_ID\": 1426,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"LED device characteristic\",\n        \"primary_unit\": \"mA/cm2\",\n        \"secondary_name\": \"bias\",\n        \"secondary_unit\": \"V\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Growth and Anion Exchange Conversion of CH3NH3PbX3 Nanorod Arrays for Light-Emitting Diodes\",\n        \"journal\": \"Nano Letters\",\n        \"vol\": \"15\",\n        \"pages_start\": \"5519\",\n        \"pages_end\": \"5524\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"CH3NH3PbBr3\",\n        \"synthesis_product\": \"CH3NH3PbI3\",\n        \"synthesis_description\": \"The hybrid perovskite (CH3NH3PbBr3) was converted at low temperature via anion exchange to produce a CH3NH3PbI3.\",\n        \"experimental_method\": \"I-V Test Device\",\n        \"experimental_description\": \"The I-V characteristics of CH3NH3PbI3 were determined by using a Keithley 2636 source-measure unit, which was coupled to a 60X objective in an inverted microscope. This was performed by with a set up of a 100 ms pulse as the device was electrically contacted a soft probe (Picoprobe T 4-10)\\r\\ncoated with indium gallium eutectic (Aldrich).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1428,\n        \"id\": 374,\n        \"compound_name\": \"3-(aminomethyl)piperidinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"3-(aminomethyl)piperidinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2 (98%), hydrobromic acid (HBr, 48%), formamidine acetate (99%), 3-(aminomethyl)piperidine\",\n        \"synthesis_product\": \"yellow plate-like crystals\",\n        \"synthesis_description\": \"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, fomamidinium acetate (312 mg, 3 mmol) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg (0.5 mmol) of 3-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5- 10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"A STOE IPDS 2 or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1429,\n        \"id\": 374,\n        \"compound_name\": \"3-(aminomethyl)piperidinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"3-(aminomethyl)piperidinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1430,\n        \"id\": 374,\n        \"compound_name\": \"3-(aminomethyl)piperidinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"3-(aminomethyl)piperidinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0261981\",\n        \"dataset_ID\": 1431,\n        \"id\": 375,\n        \"compound_name\": \"Trimethylammonioethylammonium tin iodide\",\n        \"formula\": \"C5H16N2SnI4\",\n        \"group\": \"(TMAEA)SnI4, ((CH3)3NCH2CH2NH3)SnI4, Trimethylammonioethylammonium tetraiodostannate(II)\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"N,N,N-trimethylethane-1,2-diaminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)3NCH2CH2NH3]SnI4:\\u2009 A Layered Perovskite with Quaternary/Primary Ammonium Dications and Short Interlayer Iodine\\u2212Iodine Contacts\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"1400\",\n        \"pages_end\": \"1402\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"Tin iodide, 2-trimethylammonioethylammonium diiodide, methanol, acetonitrile\",\n        \"synthesis_product\": \"Black plate-like crystals\",\n        \"synthesis_description\": \"Tin(II) iodide and trimethylammonioethylammonium diiodide were combined with methanol and acetonitrile. After 2 hours of stirring the solution became yellow and transparent, and passed through a filter with pore sizes of 0.2 microns. The solvent was allowed to evaporate at room temperature for 2-3 days, leaving behind chunky, black crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal XRD was performed at room temperature using a Bruker SMART CCD diffractometer. A normal focus 2.4 kW sealed tube X-ray source (Mo K\\u03b1 radiation) was used. The crystal structure was solved by direct methods and refined on F2 using the SHELXL 97 package.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0261981\",\n        \"dataset_ID\": 1432,\n        \"id\": 375,\n        \"compound_name\": \"Trimethylammonioethylammonium tin iodide\",\n        \"formula\": \"C5H16N2SnI4\",\n        \"group\": \"(TMAEA)SnI4, ((CH3)3NCH2CH2NH3)SnI4, Trimethylammonioethylammonium tetraiodostannate(II)\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"N,N,N-trimethylethane-1,2-diaminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1433\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)3NCH2CH2NH3]SnI4:\\u2009 A Layered Perovskite with Quaternary/Primary Ammonium Dications and Short Interlayer Iodine\\u2212Iodine Contacts\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"1400\",\n        \"pages_end\": \"1402\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"Tin iodide, 2-trimethylammonioethylammonium diiodide, methanol, acetonitrile, DMF\",\n        \"synthesis_product\": \"Dark red thin films on glass\",\n        \"synthesis_description\": \"Tin(II) iodide and trimethylammonioethylammonium diiodide were combined with methanol and acetonitrile. After 2 hours of stirring the solution became yellow and transparent, and passed through a filter with pore sizes of 0.2 microns. The solvent was allowed to evaporate at room temperature for 2-3 days, leaving behind chunky, black crystals. To produce thin films, the crystals were first dissolved in DMF to produce a transparent and yellow solution. 3-4 drops of the solution were put on a glass plate and heated to 155 degrees Celsius. A small puddle of about one square centimeter formed and within a minute began depositing black solid around its circumference. A caption sheet was used to spread the remaining solution evenly over the glass slide. A dark red film was formed on the glass slide and was kept at 155 degrees Celsius for another 2 minutes. XRD confirmed the formation of the layered perovskite structure.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The UV-vis absorption spectrum was measured via absorption spectroscopy at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0261981\",\n        \"dataset_ID\": 1433,\n        \"id\": 375,\n        \"compound_name\": \"Trimethylammonioethylammonium tin iodide\",\n        \"formula\": \"C5H16N2SnI4\",\n        \"group\": \"(TMAEA)SnI4, ((CH3)3NCH2CH2NH3)SnI4, Trimethylammonioethylammonium tetraiodostannate(II)\",\n        \"organic\": \"C5H16N2\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"N,N,N-trimethylethane-1,2-diaminium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1432\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(CH3)3NCH2CH2NH3]SnI4:\\u2009 A Layered Perovskite with Quaternary/Primary Ammonium Dications and Short Interlayer Iodine\\u2212Iodine Contacts\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"1400\",\n        \"pages_end\": \"1402\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"Tin iodide, 2-trimethylammonioethylammonium diiodide, methanol, acetonitrile, DMF\",\n        \"synthesis_product\": \"Dark red thin films on glass\",\n        \"synthesis_description\": \"Tin(II) iodide and trimethylammonioethylammonium diiodide were combined with methanol and acetonitrile. After 2 hours of stirring the solution became yellow and transparent, and passed through a filter with pore sizes of 0.2 microns. The solvent was allowed to evaporate at room temperature for 2-3 days, leaving behind chunky, black crystals. To produce thin films, the crystals were first dissolved in DMF to produce a transparent and yellow solution. 3-4 drops of the solution were put on a glass plate and heated to 155 degrees Celsius. A small puddle of about one square centimeter formed and within a minute began depositing black solid around its circumference. A caption sheet was used to spread the remaining solution evenly over the glass slide. A dark red film was formed on the glass slide and was kept at 155 degrees Celsius for another 2 minutes. XRD confirmed the formation of the layered perovskite structure.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The UV-vis absorption spectrum was measured via absorption spectroscopy at room temperature. The exact instrument is unknown.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1434,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of  formed.\",\n        \"experimental_method\": \"Single Crystal X-Ray Diffraction\",\n        \"experimental_description\": \"A Rigaku Mercury CCD diffractometer was used. Mo K\\u03b1 radiation was used with the \\u03c9 scan technique at 123 Kelvin. The structure was solved by direct methods with the Siemens SHELXTL Version 5 package. Full-matrix least-squares refinement on F2 was used to refine the structure.\",\n        \"physical_property\": \"123.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1436,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"projected density of states\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"Semi-empirical model: Extended Huckel Theory (EHT)\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"non-relativsitic\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"Total density of states\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1437,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1438\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"The absorption spectrum was calculated from measured reflection spectrum. Diffuse reflection spectroscopy was measured with a PE Lambda 35 UV-vis spectrophotometer with an integrating sphere at 273 Kelvin, and BaSO4 was the reference. The Kubelka-Munk function was used to calculate the absorption spectrum, and direct extrapolation was used to find the band gap value.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1438,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1437\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"The absorption spectrum was calculated from measured reflection spectrum. Diffuse reflection spectroscopy was measured with a PE Lambda 35 UV-vis spectrophotometer with an integrating sphere at 273 Kelvin, and BaSO4 was the reference. The Kubelka-Munk function was used to calculate the absorption spectrum, and direct extrapolation was used to find the band gap value.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1439,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1440\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals of the new type of perovskite formed.\",\n        \"experimental_method\": \"Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"PL and PL excitation spectra were measured using a JY Fluorlog-322 at room temperature. PL was measured with an excitation wavelength of 371 nm. PLE was measured at emission wavelengths of 440 and 501 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1440,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1439\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals formed.\",\n        \"experimental_method\": \"Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"PL and PL excitation spectra were measured using a JY Fluorlog-322 at room temperature. PL was measured with an excitation wavelength of 371 nm. PLE was measured at emission wavelengths of 440 and 501 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1441,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15, and after the two days and upon cooling, yellow crystals formed.\",\n        \"experimental_method\": \"Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"PL and PL excitation spectra were measured using a JY Fluorlog-322 at room temperature. PL was measured with an excitation wavelength of 371 nm. PLE was measured at emission wavelengths of 440 and 501 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"440 nm emission\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic061555j\",\n        \"dataset_ID\": 1442,\n        \"id\": 376,\n        \"compound_name\": \"Ethylenediammonium oxalate lead iodide tetrahydrate\",\n        \"formula\": \"[(H2en)7(C2O4)2](Pb4I18)\\u00b74H2O\",\n        \"group\": \"Ethylenediammonium oxalate octodecaiodo tetraplumbate(II) tetrahydrate\",\n        \"organic\": \"C18H78N14O12\",\n        \"inorganic\": \"Pb4I18, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[(H2en)7(C2O4)2] n (Pb4I18) n \\u00b74nH2O, a New Type of Perovskite Co-templated by Both Organic Cations and Anions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"45\",\n        \"pages_start\": \"10028\",\n        \"pages_end\": \"10030\",\n        \"year\": \"2006\",\n        \"synthesis_starting_materials\": \"PbI2, K2C2O4\\u00b7H2O, ethylendiamine, HI, ethanol\",\n        \"synthesis_product\": \"Yellow crystals\",\n        \"synthesis_description\": \"PbI2, K2C2O4\\u00b7H2O, and ethylendiamine was mixed into a solution of HI and ethanol at 120 degrees Celsius for 2 days. The molar ratio was 1:1:15 and after the two days and upon cooling, yellow crystals formed.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"TGA was performed on a Netzsch Sta449C thermoanalyzer in a nitrogen atmosphere over the range of 25-1000 degrees Celsius at a heating rate of 15 degrees per minute. This is dynamic thermogravimetry.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1453,\n        \"id\": 477,\n        \"compound_name\": \"Hexaflourobenzene bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4:C6F6\",\n        \"group\": \"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H12N, C6F6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"hexafluorobenzene bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            179\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, hexafluorobenzene, (PEA)2SnI4\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals of (PEA)2SnI4 intercalated with hexafluorobenzene were prepared by mixing the base layered perovskite with methanol. Then an excess of hexafluorobenzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data was collected with the Bruker SMART CCD diffractometer using 2.4 kW tube X-ray source (Mo K\\u03b1 radiation).\",\n        \"physical_property\": \"199.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1454,\n        \"id\": 477,\n        \"compound_name\": \"Hexaflourobenzene bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4:C6F6\",\n        \"group\": \"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H12N, C6F6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"hexafluorobenzene bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            179\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1455\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, hexafluorobenzene, (PEA)2SnI4\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"Films of the intercalated layered perovskites were prepared by immersing the uninteracalated films in a benzene or hexafluorobenzene solution at room temperature for an hour. The films were encapsulated by thin polycarbonate sheet while still wet from their immersion. The encapsulation effectively laminates the hybrid film and provided a partial diffusion barrier for the intercalated species. XRD and optical measurements can be made through the polycarbonate sheet cover.\",\n        \"experimental_method\": \"UV-vis Absorption\",\n        \"experimental_description\": \"Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1455,\n        \"id\": 477,\n        \"compound_name\": \"Hexaflourobenzene bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4:C6F6\",\n        \"group\": \"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H12N, C6F6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"hexafluorobenzene bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            179\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1454\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, hexafluorobenzene, (PEA)2SnI4\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"Films of the intercalated layered perovskites were prepared by immersing the uninteracalated films in a benzene or hexafluorobenzene solution at room temperature for an hour. The films were encapsulated by thin polycarbonate sheet while still wet from their immersion. The encapsulation effectively laminates the hybrid film and provided a partial diffusion barrier for the intercalated species. XRD and optical measurements can be made through the polycarbonate sheet cover.\",\n        \"experimental_method\": \"UV-vis Absorption\",\n        \"experimental_description\": \"Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1456,\n        \"id\": 477,\n        \"compound_name\": \"Hexaflourobenzene bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4:C6F6\",\n        \"group\": \"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H12N, C6F6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"hexafluorobenzene bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            179\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, hexafluorobenzene, (PEA)2SnI4\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals of (PEA)2SnI4 intercalated with hexafluorobenzene were prepared by mixing the base layered perovskite with methanol. Then an excess of hexafluorobenzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1457,\n        \"id\": 477,\n        \"compound_name\": \"Hexaflourobenzene bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4:C6F6\",\n        \"group\": \"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H12N, C6F6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"hexafluorobenzene bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            179\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"thermal transition behavior\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, hexafluorobenzene, (PEA)2SnI4\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals of (PEA)2SnI4 intercalated with hexafluorobenzene were prepared by mixing the base layered perovskite with methanol. Then an excess of hexafluorobenzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry (DSC)\",\n        \"experimental_description\": \"DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1458,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1459\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and also rectrystallized twice from a solution of methanol and toluene. \\r\\nTo produce films of the unintercalated systems, the recrystallized perovskites were dissolved in distilled methanol. Previously cleaned and prepared quartz substrates were used and the solution was spin coated onto them. The spinning cycle was 1 s ramp up to 1800 rpm, and then 30 s at 1800 rpm. Then the samples were annealed at 70 degrees Celsius for 15 minutes to remove any residual solvent.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1459,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1458\n        ],\n        \"primary_name\": \"absorption peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",\n        \"synthesis_product\": \"Thin film on quartz substrate\",\n        \"synthesis_description\": \"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and also rectrystallized twice from a solution of methanol and toluene. To produce films of the unintercalated systems, the recrystallized perovskites were dissolved in distilled methanol. Previously cleaned and prepared quartz substrates were used and the solution was spin coated onto them. The spinning cycle was 1 s ramp up to 1800 rpm, and then 30 s at 1800 rpm. Then the samples were annealed at 70 degrees Celsius for 15 minutes to remove any residual solvent.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Absorption spectra were measured with a Hewlett-Packard UV-vis 8543 spectrophotometer at room temperature on the quartz thin-film samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1460,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and recrystallized twice from a solution of methanol and toluene.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1461,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"thermal transition behavior\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"HI, SnI2, phenylethylammonium iodide (PEAI), toluene\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals were grown by slowly cooling a solution of HI and PEAI and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and also rectrystallized twice from a solution of methanol and toluene.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry (DSC)\",\n        \"experimental_description\": \"DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1463,\n        \"id\": 378,\n        \"compound_name\": \"2,3,4,5,6-pentafluorophenethylammoniom tin iodide : Benzene\",\n        \"formula\": \"C22H20N2F10SnI4\",\n        \"group\": \"(2,3,4,5,6-FPEA)2SnI4\\u00ac\\u2211(C6H6), (C6F5(CH2)2NH3)2SnI4\\u00ac\\u2211(C6H6), benzene-intercalated 2,3,4,5,6-pentafluorophenethylammonium tin iodide, benzene 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H7NF5, C6H6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"benzene 2,3,4,5,6-pentafluorophenethanaminium tin iodide\",\n        \"last_update\": \"2022-06-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, benzene, (C6F5C2H4NH3)2SnI4\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals of (2,3,4,5,6-FPEA)2SnI4 intercalated with benzene were prepared by mixing the base layered perovskite with methanol. Then an excess of benzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data was collected with the Bruker SMART CCD diffractometer using 2.4 kW tube X-ray source (Mo K\\u03b1 radiation).\",\n        \"physical_property\": \"199.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1464,\n        \"id\": 378,\n        \"compound_name\": \"2,3,4,5,6-pentafluorophenethylammoniom tin iodide : Benzene\",\n        \"formula\": \"C22H20N2F10SnI4\",\n        \"group\": \"(2,3,4,5,6-FPEA)2SnI4\\u00ac\\u2211(C6H6), (C6F5(CH2)2NH3)2SnI4\\u00ac\\u2211(C6H6), benzene-intercalated 2,3,4,5,6-pentafluorophenethylammonium tin iodide, benzene 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H7NF5, C6H6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"benzene 2,3,4,5,6-pentafluorophenethanaminium tin iodide\",\n        \"last_update\": \"2022-06-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, benzene, (C6F5C2H4NH3)2SnI4\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals of (2,3,4,5,6-FPEA)2SnI4 intercalated with benzene were prepared by mixing the base layered perovskite with methanol. Then an excess of benzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1465,\n        \"id\": 378,\n        \"compound_name\": \"2,3,4,5,6-pentafluorophenethylammoniom tin iodide : Benzene\",\n        \"formula\": \"C22H20N2F10SnI4\",\n        \"group\": \"(2,3,4,5,6-FPEA)2SnI4\\u00ac\\u2211(C6H6), (C6F5(CH2)2NH3)2SnI4\\u00ac\\u2211(C6H6), benzene-intercalated 2,3,4,5,6-pentafluorophenethylammonium tin iodide, benzene 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H7NF5, C6H6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"benzene 2,3,4,5,6-pentafluorophenethanaminium tin iodide\",\n        \"last_update\": \"2022-06-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"thermal transition behavior\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"Methanol, benzene, (C6F5C2H4NH3)2SnI4\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals of (2,3,4,5,6-FPEA)2SnI4 intercalated with benzene were prepared by mixing the base layered perovskite with methanol. Then an excess of benzene was added to the solution and the solution was stirred until it became homogenous and yellow. Then it sat in an inert atmosphere for a few days and red, plate-like crystals of the system formed.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry (DSC)\",\n        \"experimental_description\": \"DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1466,\n        \"id\": 379,\n        \"compound_name\": \"2,3,4,5,6-pentafluorophenethylammoniom tin iodide\",\n        \"formula\": \"C16H14N2F10SnI4\",\n        \"group\": \"(2,3,4,5,6-FPEA)2SnI4, (C6F5(CH2)2NH3)2SnI4, 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H7NF5\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"2,3,4,5,6-pentafluorophenethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"HI, SnI2, C6F5C2H4NH3I, toluene\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals were grown by slowly cooling a solution of HI, C6F5C2H4NH3I, and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and recrystallized twice from a solution of methanol and toluene.\",\n        \"experimental_method\": \"Thermogravimetric Analysis (TGA)\",\n        \"experimental_description\": \"TGA was performed with a TA Instruments TGA-2950 on the crystals that were isothermally purged in a nitrogen atmosphere at ambient temperature for 20 minutes. The temperature was then increased at a constant rate of 5 degress Celsius per minute up to 600 degrees.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic011190x\",\n        \"dataset_ID\": 1467,\n        \"id\": 379,\n        \"compound_name\": \"2,3,4,5,6-pentafluorophenethylammoniom tin iodide\",\n        \"formula\": \"C16H14N2F10SnI4\",\n        \"group\": \"(2,3,4,5,6-FPEA)2SnI4, (C6F5(CH2)2NH3)2SnI4, 2,3,4,5,6-pentafluorophenethanaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H7NF5\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"2,3,4,5,6-pentafluorophenethanaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"thermal transition behavior\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Intercalated Organic\\u2212Inorganic Perovskites Stabilized by Fluoroaryl\\u2212Aryl Interactions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"41\",\n        \"pages_start\": \"2134\",\n        \"pages_end\": \"2145\",\n        \"year\": \"2002\",\n        \"synthesis_starting_materials\": \"HI, SnI2, C6F5C2H4NH3I, toluene\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"Crystals were grown by slowly cooling a solution of HI, C6F5C2H4NH3I, and SnI2. SnI2 was added first, then the organic salt, and then HI. The solution was mixed and heated to 94 degrees Celsius to completely dissolve SnI2. The solution was then cooled at 3 degrees per hour until 0 degrees was reached, resulting in the formation of red crystals. The crystals were filtered in an inert atmosphere and recrystallized twice from a solution of methanol and toluene.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry (DSC)\",\n        \"experimental_description\": \"DSC was performed with a TA Instruments MDSC-2920. A heating rate of 5 degrees per minute weas used and the temperature scale was calibrated using the indium melting transition. This is power-compensated DSC where the heating rate and power supply is constant.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevLett.121.146401\",\n        \"dataset_ID\": 1469,\n        \"id\": 22,\n        \"compound_name\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead iodide\",\n        \"formula\": \"C20H22N2S4PbI4\",\n        \"group\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene tetraiodoplumbate(II), AE4TPbI4, (AEQT)PbI4, AEQTPbI4, C20H22S4N2PbI4\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'''-bis(aminoethyl)-2,2':5',2'':5'',2'''-quaterthiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tunable Semiconductors: Control over Carrier States and Excitations in Layered Hybrid Organic-Inorganic Perovskites\",\n        \"journal\": \"Physical Review Letters\",\n        \"vol\": \"121\",\n        \"pages_start\": \"146401-1\",\n        \"pages_end\": \"146401-6\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1470,\n        \"id\": 374,\n        \"compound_name\": \"3-(aminomethyl)piperidinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"3-(aminomethyl)piperidinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1471,\n        \"id\": 374,\n        \"compound_name\": \"3-(aminomethyl)piperidinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(3AMP)(FA)Pb2Br7, 3-(aminomethyl)piperidinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"3-(aminomethyl)piperidinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1472,\n        \"id\": 380,\n        \"compound_name\": \"3-(aminomethyl)piperindinium methylammonium lead bromide\",\n        \"formula\": \"(C6N2H16)(CH3NH3)Pb2Br7\",\n        \"group\": \"(3AMP)(MA)Pb2Br7, 3-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH6N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"3-(methanaminium)piperindinium methanaminium lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2 (98%), hydrobromic acid (HBr, 48%), methylammonium chloride (\\u226598%), 3-(aminomethyl)piperidine\",\n        \"synthesis_product\": \"yellow plate-like crystals\",\n        \"synthesis_description\": \"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, methylammonium chloride (202 mg) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg (0.5 mmol) of 3-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5- 10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"A STOE IPDS 2 or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1473,\n        \"id\": 381,\n        \"compound_name\": \"4-(aminomethyl)piperindinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2 (98%), hydrobromic acid (HBr, 48%), formamidine acetate (99%), 4-(aminomethyl)piperidine (96%)\",\n        \"synthesis_product\": \"yellow, plate-like crystals\",\n        \"synthesis_description\": \"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, fomamidinium acetate (312 mg, 3 mmol) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg of 4-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5-10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"A STOE IPDS 2 or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1474,\n        \"id\": 381,\n        \"compound_name\": \"4-(aminomethyl)piperindinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1475,\n        \"id\": 381,\n        \"compound_name\": \"4-(aminomethyl)piperindinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1476,\n        \"id\": 381,\n        \"compound_name\": \"4-(aminomethyl)piperindinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1477,\n        \"id\": 381,\n        \"compound_name\": \"4-(aminomethyl)piperindinium formamidinium lead bromide\",\n        \"formula\": \"(C6N2H16)[HC(NH2)2]Pb2Br7\",\n        \"group\": \"(4AMP)(FA)Pb2Br7, 4-(methanaminium)piperindinium diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH5N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"Data was collected with a HORIBA LabRAM HR Evolution Confocal RAMAN microscope. A laster (473 nm, 25 mW, 0.1% power) was used to excite samples.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Pc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1478,\n        \"id\": 382,\n        \"compound_name\": \"4-(aminomethyl)piperindinium methylammonium lead bromide\",\n        \"formula\": \"(C6N2H16)(CH3NH3)Pb2Br7\",\n        \"group\": \"(4AMP)(MA)Pb2Br7, 4-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH6N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium methanaminium lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2 (98%), hydrobromic acid (HBr, 48%), methylammonium chloride (\\u226598%), 4-(aminomethyl)piperidine (96%)\",\n        \"synthesis_product\": \"yellow plate-like crystals\",\n        \"synthesis_description\": \"First, PbBr2 (1.10 g, 3 mmol) was dissolved in 5 mL of HBr in one vial. Next, methylammonium chloride (202 mg) was added to the solution. In a separate vial, HBr (1 mL) was added to 57 mg of 4-(aminomethyl)piperidine. The solution was heated and stirred, and this solution was poured into the PbBr2 solution. The reaction continued for 5- 10 minutes, and the total solution became clear. Plate-like yellow crystals precipitated as the solution cooled to ambient temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"A STOE IPDS 2 or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 A, 50 kV, 40 mA) was used. The data was collected in N2 at 293 K. Frames were collected, integrated, and corrected for absorption with the STOE X-AREA program.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1479,\n        \"id\": 382,\n        \"compound_name\": \"4-(aminomethyl)piperindinium methylammonium lead bromide\",\n        \"formula\": \"(C6N2H16)(CH3NH3)Pb2Br7\",\n        \"group\": \"(4AMP)(MA)Pb2Br7, 4-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH6N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium methanaminium lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c01625\",\n        \"dataset_ID\": 1480,\n        \"id\": 382,\n        \"compound_name\": \"4-(aminomethyl)piperindinium methylammonium lead bromide\",\n        \"formula\": \"(C6N2H16)(CH3NH3)Pb2Br7\",\n        \"group\": \"(4AMP)(MA)Pb2Br7, 4-(methanaminium)piperindinium methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C6N2H16, CH6N\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"4-(methanaminium)piperindinium methanaminium lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic Cation Alloying on Intralayer A and Interlayer A\\u2019 sites in 2D Hybrid Dion\\u2212Jacobson Lead Bromide Perovskites (A\\u2019)(A)Pb2Br7\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"8342\",\n        \"pages_end\": \"8351\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1481,\n        \"id\": 383,\n        \"compound_name\": \"Pyridiniumethylammonium lead iodide\",\n        \"formula\": \"C7H14I4N2Pb\",\n        \"group\": \"(PyrEA)[PbI4]\",\n        \"organic\": \"C7H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyridin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"pyridine, iodoethylammonium iodide, anhydrous acetonitrile, PbI2, HI\",\n        \"synthesis_product\": \"red plate crystals\",\n        \"synthesis_description\": \"First, PyrEAI was synthesized by charging a flamed-dried two-neck round bottom flask with pyridine (1.05 equivalent), iodoethylammonium iodide (1.00 equivalent), and anhydrous acetonitrile (which was dried with CaH2 before distillation). The mixture was heated and stirred at reflux for 2 days. The mixture was then cooled to room temperature. The precipitate was isolated by filtration, washed with diethyl ether, and dried. \\r\\nThen, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and PyrEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140\\u00baC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo K\\u03b1 radiation (0.71073\\u00c5) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1482,\n        \"id\": 383,\n        \"compound_name\": \"Pyridiniumethylammonium lead iodide\",\n        \"formula\": \"C7H14I4N2Pb\",\n        \"group\": \"(PyrEA)[PbI4]\",\n        \"organic\": \"C7H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyridin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Wavelength used was \\u03bb = 0.71073 \\u00c5.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1483,\n        \"id\": 383,\n        \"compound_name\": \"Pyridiniumethylammonium lead iodide\",\n        \"formula\": \"C7H14I4N2Pb\",\n        \"group\": \"(PyrEA)[PbI4]\",\n        \"organic\": \"C7H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyridin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Band gap data was obtained by linear-fitting the UV-vis absorption spectra.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1484,\n        \"id\": 383,\n        \"compound_name\": \"Pyridiniumethylammonium lead iodide\",\n        \"formula\": \"C7H14I4N2Pb\",\n        \"group\": \"(PyrEA)[PbI4]\",\n        \"organic\": \"C7H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyridin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PyrEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1485,\n        \"id\": 383,\n        \"compound_name\": \"Pyridiniumethylammonium lead iodide\",\n        \"formula\": \"C7H14I4N2Pb\",\n        \"group\": \"(PyrEA)[PbI4]\",\n        \"organic\": \"C7H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyridin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"cm^{-1}\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PyrEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"UV-Vis spectroscopy and scanning electron microscopy\",\n        \"experimental_description\": \"UV-vis absorption spectra were recorded using a SHIMADZU UV-3600 spectrophotometer, with an integrating sphere (ISR-3100) in the wavelength range 300-800nm. Film thickness was calculated by cross-section images of the thin films recorded using a JEOL JSM-7600F field emission scanning electron microscope (FESEM), with an accelerating voltage of 5kV. Absorption coefficients at each wavelength were calculated by \\u03b1(\\u03bb) = 1/d * ln([1-R(\\u03bb)]/[T(\\u03bb)]). Here, \\u03b1 is the absorption coefficient, R is the reflectance, and T is the transmittance. [1]\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1486,\n        \"id\": 383,\n        \"compound_name\": \"Pyridiniumethylammonium lead iodide\",\n        \"formula\": \"C7H14I4N2Pb\",\n        \"group\": \"(PyrEA)[PbI4]\",\n        \"organic\": \"C7H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyridin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PyrEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"steady-state PL spectroscopy\",\n        \"experimental_description\": \"Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1487,\n        \"id\": 384,\n        \"compound_name\": \"Imidazoliumethylammonium lead iodide\",\n        \"formula\": \"C5H13I4N3Pb\",\n        \"group\": \"(ImEA)[PbI4]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-imidazol-3-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"ImEAI, PbI2, HI\",\n        \"synthesis_product\": \"orange plate\",\n        \"synthesis_description\": \"ImEAI was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and ImEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140\\u00baC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo K\\u03b1 radiation (0.71073\\u00c5) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1488,\n        \"id\": 384,\n        \"compound_name\": \"Imidazoliumethylammonium lead iodide\",\n        \"formula\": \"C5H13I4N3Pb\",\n        \"group\": \"(ImEA)[PbI4]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-imidazol-3-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Wavelength used was \\u03bb = 0.71073 \\u00c5.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1489,\n        \"id\": 384,\n        \"compound_name\": \"Imidazoliumethylammonium lead iodide\",\n        \"formula\": \"C5H13I4N3Pb\",\n        \"group\": \"(ImEA)[PbI4]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-imidazol-3-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1490,\n        \"id\": 384,\n        \"compound_name\": \"Imidazoliumethylammonium lead iodide\",\n        \"formula\": \"C5H13I4N3Pb\",\n        \"group\": \"(ImEA)[PbI4]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-imidazol-3-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"(ImEA)[PbI4] (synthesized), DMF\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and were spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1491,\n        \"id\": 384,\n        \"compound_name\": \"Imidazoliumethylammonium lead iodide\",\n        \"formula\": \"C5H13I4N3Pb\",\n        \"group\": \"(ImEA)[PbI4]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-imidazol-3-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1492,\n        \"id\": 384,\n        \"compound_name\": \"Imidazoliumethylammonium lead iodide\",\n        \"formula\": \"C5H13I4N3Pb\",\n        \"group\": \"(ImEA)[PbI4]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-imidazol-3-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"cm^{-1}\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (ImEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Absorption coefficients at each wavelength were calculated by \\u03b1(\\u03bb) = 1/d(film) * ln([1-Rfilm(\\u03bb)]/[Tfilm(\\u03bb)])\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/c1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1494,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PEA)2PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"Optical absorbtion\",\n        \"experimental_description\": \"Wavelength was \\u03bb = 0.71073 \\u00c5.\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C1c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1495,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, transmission)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"(PEA)2PbI4 (synthesized), DMF\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PEA)2PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"the spectrum was recorded using SHIMADZU   UV-3600.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1496,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Stokes shift\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C1c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1497,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"cm^{-1}\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"Thin-film of thickness 338 nm\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PEA)2PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"UV-Vis spectroscopy and scanning electron microscopy\",\n        \"experimental_description\": \"UV-vis absorption spectra were recorded using a SHIMADZU UV-3600 spectrophotometer, with an integrating sphere (ISR-3100) in the wavelength range 300-800nm. Film thickness was calculated by cross-section images of the thin films recorded using a JEOL JSM-7600F field emission scanning electron microscope (FESEM), with an accelerating voltage of 5kV.\\r\\nAbsorption coefficients at each wavelength were calculated by \\u03b1(\\u03bb) = 1/d * ln([1-R(\\u03bb)]/[T(\\u03bb)]). Here, \\u03b1 is the absorption coefficient, R is the reflectance, and T is the transmittance. [1]\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C1c1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1498,\n        \"id\": 385,\n        \"compound_name\": \"Pyrazoliumethylammonium lead iodide\",\n        \"formula\": \"C20H52I20N12O4Pb6\",\n        \"group\": \"(PyrzEA)[Pb2I6]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyrazol-2-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PyrzEAI, PbI2, HI\",\n        \"synthesis_product\": \"yellow prism\",\n        \"synthesis_description\": \"PipEAI was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and PyrzEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140\\u00baC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo K\\u03b1 radiation (0.71073\\u00c5) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C12/c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1499,\n        \"id\": 385,\n        \"compound_name\": \"Pyrazoliumethylammonium lead iodide\",\n        \"formula\": \"C20H52I20N12O4Pb6\",\n        \"group\": \"(PyrzEA)[Pb2I6]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyrazol-2-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PyrzEA)[Pb2I6] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Wavelength used was \\u03bb = 0.71073 \\u00c5.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C12/c1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1500,\n        \"id\": 385,\n        \"compound_name\": \"Pyrazoliumethylammonium lead iodide\",\n        \"formula\": \"C20H52I20N12O4Pb6\",\n        \"group\": \"(PyrzEA)[Pb2I6]\",\n        \"organic\": \"C5H13N3\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-pyrazol-2-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PyrzEA)[Pb2I6] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1501,\n        \"id\": 263,\n        \"compound_name\": \"Histammonium lead iodide\",\n        \"formula\": \"(C5H11N3)PbI4\",\n        \"group\": \"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (HA)PbI4 (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/n1\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1502,\n        \"id\": 263,\n        \"compound_name\": \"Histammonium lead iodide\",\n        \"formula\": \"(C5H11N3)PbI4\",\n        \"group\": \"(HA)PbI4, 4-(2-ethanaminium)-1H-imidazol-3-ium tetraiodoplumbate(II)\",\n        \"organic\": \"C5H11N3\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-(2-ethanaminium)-1H-imidazol-3-ium lead (II) iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"histamine dihydrochloride, HI, PbI2\",\n        \"synthesis_product\": \"red block\",\n        \"synthesis_description\": \"Histamine dihydrochloride was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and HA were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140\\u00baC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo K\\u03b1 radiation (0.71073\\u00c5) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/n1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1503,\n        \"id\": 386,\n        \"compound_name\": \"piperidiniumethylammonium lead iodide\",\n        \"formula\": \"C14H34I8N4Pb2\",\n        \"group\": \"(PipEA)[PbI4]\",\n        \"organic\": \"C7H20N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-piperidin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PipEAI, PbI2, HI\",\n        \"synthesis_product\": \"red plate\",\n        \"synthesis_description\": \"PipEAI was purchased from Sigma Aldrich. Then, stoichiometric amounts of PbI2 (purchased from Sigma Aldrich) and PipEAI were added to concentrated stabilized aqueous HI. The concentration of the solution was maintained at 0.25-0.30M of Pb2+. The solution was heated at 140\\u00baC and stirred for an hour. The resulting clear solution was cooled slowly to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo K\\u03b1 radiation (0.71073\\u00c5) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/n1\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1504,\n        \"id\": 386,\n        \"compound_name\": \"piperidiniumethylammonium lead iodide\",\n        \"formula\": \"C14H34I8N4Pb2\",\n        \"group\": \"(PipEA)[PbI4]\",\n        \"organic\": \"C7H20N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-piperidin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Wavelength used was \\u03bb = 0.71073 \\u00c5.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/n1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1505,\n        \"id\": 386,\n        \"compound_name\": \"piperidiniumethylammonium lead iodide\",\n        \"formula\": \"C14H34I8N4Pb2\",\n        \"group\": \"(PipEA)[PbI4]\",\n        \"organic\": \"C7H20N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-piperidin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Data was collected with a SHIMADZU UV-3600 spectrophotometer and an integrated sphere (ISR-3100) in the wavelength range 300-800 nm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/n1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1506,\n        \"id\": 386,\n        \"compound_name\": \"piperidiniumethylammonium lead iodide\",\n        \"formula\": \"C14H34I8N4Pb2\",\n        \"group\": \"(PipEA)[PbI4]\",\n        \"organic\": \"C7H20N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-piperidin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"steady-state PL spectroscopy\",\n        \"experimental_description\": \"Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1507,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead(II) iodide, 2-phenethylamine (PEA), HI, diethyl ether\",\n        \"synthesis_product\": \"orange needle-like crystals\",\n        \"synthesis_description\": \"a round bottom flask containing ethanol and PEA was cooled to 0 degree C. To it, a stoichiometric amount of concentrated hydroiodic acid was added. After stirring the solution for 1 hour, all volatiles were removed using a rotary evaporator. The remaining solid is PEAI salt. It was washed with diethyl ether and dried under vacuum at 50\\u00b0C overnight.\\r\\n\\r\\nStoichiometric amounts of PbI2 and PEAI were added to concentrated stabilized aqueous HI (concentrations of around 0.25-0.30M of Pb2+). The solution was heated and stirred at 140\\u00baC for an hour, and the clear solutions cooled slowly to room temperature.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Data was collected with a BrukerX8 CCD area detector diffractometer, with Mo K\\u03b1 radiation (0.71073\\u00c5) at 100 K. SAINT and SADABS packages were used for data reduction and absorption corrections, respectively.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpcc.7b00890\",\n        \"dataset_ID\": 1509,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Ab Initio, Quantum Espresso\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (supplemented by D2 method)\",\n        \"k_point_grid\": \"4x4x1\",\n        \"level_of_relativity\": \"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",\n        \"basis_set_definition\": \"SRL pseudopotentials with Opium\",\n        \"numerical_accuracy\": \"Wave functions have energy cutoff of 680 eV\",\n        \"title\": \"Influence of the Dimensionality and Organic Cation on Crystal and Electronic Structure of Organometalic Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry\",\n        \"vol\": \"121\",\n        \"pages_start\": \"6569\",\n        \"pages_end\": \"6574\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpcc.7b00890\",\n        \"dataset_ID\": 1510,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Ab Initio, Quantum Espresso\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE supplemented by D2 method\",\n        \"k_point_grid\": \"4x4x1\",\n        \"level_of_relativity\": \"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",\n        \"basis_set_definition\": \"SRL pseudopotentials with Opium\",\n        \"numerical_accuracy\": \"Wave functions have energy cut off of 680 eV\",\n        \"title\": \"Influence of the Dimensionality and Organic Cation on Crystal and Electronic Structure of Organometalic Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry\",\n        \"vol\": \"121\",\n        \"pages_start\": \"6569\",\n        \"pages_end\": \"6574\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpcc.7b00890\",\n        \"dataset_ID\": 1511,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Ab Initio, Quantum Espresso\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE supplemented by D2 method\",\n        \"k_point_grid\": \"4x4x1\",\n        \"level_of_relativity\": \"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",\n        \"basis_set_definition\": \"SRL pseudopotentials with Opium\",\n        \"numerical_accuracy\": \"Wave functions have energy cut off of 680 eV\",\n        \"title\": \"Influence of the Dimensionality and Organic Cation on Crystal and Electronic Structure of Organometalic Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry\",\n        \"vol\": \"121\",\n        \"pages_start\": \"6569\",\n        \"pages_end\": \"6574\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpcc.7b00890\",\n        \"dataset_ID\": 1512,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Ab Initio, Quantum Espresso\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE supplemented by D2 method\",\n        \"k_point_grid\": \"4x4x1\",\n        \"level_of_relativity\": \"Relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",\n        \"basis_set_definition\": \"SRL pseudopotentials with Opium\",\n        \"numerical_accuracy\": \"wave functions have energy cut off of 680 eV\",\n        \"title\": \"Influence of the Dimensionality and Organic Cation on Crystal and Electronic Structure of Organometalic Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry\",\n        \"vol\": \"121\",\n        \"pages_start\": \"6569\",\n        \"pages_end\": \"6574\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpcc.7b00890\",\n        \"dataset_ID\": 1513,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Ab Initio, Quantum Espresso\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE supported by D2 method\",\n        \"k_point_grid\": \"4x4x1\",\n        \"level_of_relativity\": \"relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",\n        \"basis_set_definition\": \"SRL pseudopotentials with Opium\",\n        \"numerical_accuracy\": \"wave functions have energy cut off of 680 eV\",\n        \"title\": \"Influence of the Dimensionality and Organic Cation on Crystal and Electronic Structure of Organometalic Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry\",\n        \"vol\": \"121\",\n        \"pages_start\": \"6569\",\n        \"pages_end\": \"6574\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpcc.7b00890\",\n        \"dataset_ID\": 1514,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Ab Initio, Quantum Espresso\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE supplemented by D2 method\",\n        \"k_point_grid\": \"4x4x4\",\n        \"level_of_relativity\": \"relativistic effects , including SOC, are treated for core orbitals. Splitting due to SOC is averaged in valence region\",\n        \"basis_set_definition\": \"SRL pseudopotentials with Opium\",\n        \"numerical_accuracy\": \"wave functions have energy cut off of 680 eV\",\n        \"title\": \"Influence of the Dimensionality and Organic Cation on Crystal and Electronic Structure of Organometalic Halide Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry\",\n        \"vol\": \"121\",\n        \"pages_start\": \"6569\",\n        \"pages_end\": \"6574\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.nanolett.6b04453\",\n        \"dataset_ID\": 1517,\n        \"id\": 478,\n        \"compound_name\": \"Methylammonium lead bromide iodide\",\n        \"formula\": \"CH3NH3PbBr(x)I(3-x)\",\n        \"group\": \"MAPb(Br,I)3, MAPbBr(x)I(3-x), MAPbBrI, MAPI alloy\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"PbBr(x)I(3-x), Lead bromide iodide\",\n        \"iupac\": \"Methanaminium lead bromide iodide\",\n        \"last_update\": \"2022-04-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Origin of Reversible Photoinduced Phase Separation in Hybrid Perovskites\",\n        \"journal\": \"Nano Letters\",\n        \"vol\": \"17\",\n        \"pages_start\": \"1028\",\n        \"pages_end\": \"1033\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbBr2 (Aldrich), CH3NH3Br (Dyesol) , PbI2 (Aldrich), CH3NH3I (Dyesol), DMF (Aldrich)\",\n        \"synthesis_product\": \"CsPb(BrxI1-x)3\",\n        \"synthesis_description\": \"CsPbBr3 was synthesized from a solution containing 0.3 M of CsBr (Aldrich)/PbBr2 and CsI (Aldrich)/PbI2 in DMSO. Films of CsPbBr3 were obtained from heating and annealing the solution at 150 \\u00b0C and 75 \\u00b0C.\",\n        \"experimental_method\": \"Confocal microscopy and photoluminescence (PL) spectra\",\n        \"experimental_description\": \"The temperature dependence of phase separation with PL was measured by observing the time it took for the PL peak of  iodide-rich clusters of the compound films to reach the maximum value.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.nanolett.6b04453\",\n        \"dataset_ID\": 1518,\n        \"id\": 478,\n        \"compound_name\": \"Methylammonium lead bromide iodide\",\n        \"formula\": \"CH3NH3PbBr(x)I(3-x)\",\n        \"group\": \"MAPb(Br,I)3, MAPbBr(x)I(3-x), MAPbBrI, MAPI alloy\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"PbBr(x)I(3-x), Lead bromide iodide\",\n        \"iupac\": \"Methanaminium lead bromide iodide\",\n        \"last_update\": \"2022-04-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"time-dependent photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"time\",\n        \"secondary_unit\": \"s\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Origin of Reversible Photoinduced Phase Separation in Hybrid Perovskites\",\n        \"journal\": \"Nano Letters\",\n        \"vol\": \"17\",\n        \"pages_start\": \"1028\",\n        \"pages_end\": \"1033\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"PbBr2 (Aldrich), CH3NH3Br (Dyesol) , PbI2 (Aldrich), CH3NH3I (Dyesol), DMF (Aldrich)\",\n        \"synthesis_product\": \"CsPb(BrxI1-x)3\",\n        \"synthesis_description\": \"CsPbBr3 was synthesized from a solution containing 0.3 M of CsBr (Aldrich)/PbBr2 and CsI (Aldrich)/PbI2 in DMSO. Films of CsPbBr3 were obtained from heating and annealing the solution at 150 \\u00b0C and 75 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"The Photoluminescence Spectra method was used to measure the normalized PL intensity versus time of the iodide cluster peak by using an excitation source of 405 nm LED.\",\n        \"physical_property\": \"405.0\",\n        \"unit\": \"nm\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1038/s41467-018-07952-x\",\n        \"dataset_ID\": 1522,\n        \"id\": 390,\n        \"compound_name\": \"OITP\",\n        \"formula\": \"MAPbX3\",\n        \"group\": \"trihalide perovskites\",\n        \"organic\": \"MA\",\n        \"inorganic\": \"PbX3\",\n        \"iupac\": \"\",\n        \"last_update\": \"2020-07-27\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"Ma\",\n        \"secondary_name\": \"voltage\",\n        \"secondary_unit\": \"V\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Spin-optoelectronic devices based on hybrid organic-inorganic trihalide perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1\",\n        \"pages_end\": \"6\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbBr2 and MABr (1:1:1 molar ratio), dimethyl sulfoxide (0.5 M), ,\",\n        \"synthesis_product\": \"OITP\",\n        \"synthesis_description\": \"OITP was produced by mixing a solution of PbBr2 and MABr in a 0.5 M concentration of dimethyl sulfoxide (DMSO). The solution was coated using SOC on an O2 substrate at 4000 rpm. The films were bathed in a chloroform solvent and heated at 100 \\u00b0C until the crystals produced.\",\n        \"experimental_method\": \"Spin-LED device\",\n        \"experimental_description\": \"The spin-LED Method demonstrated an anode (MAPbBr3 spin-coated with LSMO) and a cathode (Al film coated on organic small molecules). A magnetic field was applied as spin-polarized and unpolarized electron was injected into the device, portraying measurements EL emissions and the voltage.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"I-V of MAPbBr\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.synthmet.2015.11.028\",\n        \"dataset_ID\": 1523,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular design and photovoltaic performance of a novel thiocyanate-based layered organometal perovskite material\",\n        \"journal\": \"Synthetic Metals\",\n        \"vol\": \"215\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"63\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rapid Auto diffractometer was used at 293 K to collect SCXRD data using Mo K\\u03b1 radiation (= 0.71073 \\u00c5). The structure was solved and refined with the SHELXL-software programs.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnm2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.synthmet.2015.11.028\",\n        \"dataset_ID\": 1524,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Infrared absorption spectrum\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular design and photovoltaic performance of a novel thiocyanate-based layered organometal perovskite material\",\n        \"journal\": \"Synthetic Metals\",\n        \"vol\": \"215\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"63\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.\",\n        \"experimental_method\": \"IR Spectroscopy\",\n        \"experimental_description\": \"A Themo NICOLET-380 spectrophotometer was used to measure the IR spectra over the range 4000-400 cm^(-1). The samples were prepared with the KBr pellet method.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnm2(1)\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.synthmet.2015.11.028\",\n        \"dataset_ID\": 1525,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular design and photovoltaic performance of a novel thiocyanate-based layered organometal perovskite material\",\n        \"journal\": \"Synthetic Metals\",\n        \"vol\": \"215\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"63\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",\n        \"synthesis_product\": \"Red film\",\n        \"synthesis_description\": \"MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.\",\n        \"experimental_method\": \"UV-vis absorption spectroscopy\",\n        \"experimental_description\": \"A Shimadzu UV-1800 spectrophotometer was used to measure the UV-vis absorption spectra over the range 200-800 nm at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnm2(1)\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.synthmet.2015.11.028\",\n        \"dataset_ID\": 1526,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1527\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular design and photovoltaic performance of a novel thiocyanate-based layered organometal perovskite material\",\n        \"journal\": \"Synthetic Metals\",\n        \"vol\": \"215\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"63\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",\n        \"synthesis_product\": \"Red film\",\n        \"synthesis_description\": \"MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.\",\n        \"experimental_method\": \"Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"A Horiba Flurolog 3 was used to measure the PL emission spectra of the samples by exciting at 560 nm at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnm2(1)\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.synthmet.2015.11.028\",\n        \"dataset_ID\": 1527,\n        \"id\": 88,\n        \"compound_name\": \"bis(methylammonium) lead thiocyanate iodide\",\n        \"formula\": \"C4H12N4S2PbI2\",\n        \"group\": \"bis(methanaminium) di-S-thiocyanato di-iodoplumbate(II), (MA)2Pb(SCN)2I2, (CH3NH3)2Pb(SCN)2I2\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"Pb(SCN)2I2, Lead thiocyanate iodide\",\n        \"iupac\": \"bis(methanaminium) lead (II) thiocyanate iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1526\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular design and photovoltaic performance of a novel thiocyanate-based layered organometal perovskite material\",\n        \"journal\": \"Synthetic Metals\",\n        \"vol\": \"215\",\n        \"pages_start\": \"56\",\n        \"pages_end\": \"63\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylammonium iodide (MAI), lead thiocyanide (Pb(SCN)2), DMF, tetrahydrofuran (THF)\",\n        \"synthesis_product\": \"Red film\",\n        \"synthesis_description\": \"MAI and Pb(SCN)2 (2:1 molar ratio) were mixed into a DMF solution held at 60 degrees Celsius and stirred for 6 hours. A red-brown solid precipitated and was isolated by evaporating the solvent and then dissolving the solid in a tetrahydrofuran (THF) solution. The final product was then obtained by letting the solution evaporate at 50 degrees Celsius inside a vacuum for 24 hours.\",\n        \"experimental_method\": \"Photoluminescence Spectroscopy\",\n        \"experimental_description\": \"A Horiba Flurolog 3 was used to measure the PL emission spectra of the samples by exciting at 560 nm at room temperature.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnm2(1)\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b00290\",\n        \"dataset_ID\": 1529,\n        \"id\": 273,\n        \"compound_name\": \"Propylammonium silsesquioxane copper chloride\",\n        \"formula\": \"C48H220Cl12Cu4N16O48Si32\",\n        \"group\": \"CUPOSS, propane-1-aminium silsesquioxane dodecachloro tetracuprate(II)\",\n        \"organic\": \"N/A\",\n        \"inorganic\": \"MX6\",\n        \"iupac\": \"propane-1-aminium silsesquioxane copper chloride\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layered Hybrid Perovskites with Micropores Created by Alkylammonium Functional Silsesquioxane Interlayers\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"0\",\n        \"pages_start\": \"4158\",\n        \"pages_end\": \"4163\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"A-POSS and CuCl2, PdCl2, PbCl2, or MnCl2\",\n        \"synthesis_product\": \"CuPOSS, PdPOSS, PbPOSS, MnPOSS\",\n        \"synthesis_description\": \"A- POSS and metal halides (CuCl3, PdCl2, PbCl3, and MnCl2) were either dissolved in water or hydrochloric acid and precipitated into ethanol or acetone solvents.\",\n        \"experimental_method\": \"Filtration\",\n        \"experimental_description\": \"Yellow precipitation was collected via filtration (213 mg) after A-POSS (200 mg) and CuCl2 ( 120 mg) was dissolved in water and added to a solution of ethanol (60 mL) to yield CuPOSS. An orange precipitate was collected from the synthesis of A-POSS (264 mg) and PdCl2 (99mg) in water and a 2N HCl solution (1.85 mL) and then dropped into ethanol, which formed PdPOSS. A white precipitate was collected by dissolving A-POSS (311 mg) in a 2N HCl solution and PbCl2 (300 mg)  in an HCl solution that produced PbPOSS. Likewise, a white precipitate was collected from the synthesis of A-POSS (100 mg) and MnCl2 (67 mg) that was dissolved in water (0.384 mL) and added to an acetone solution (60 mL) for the production of MnPOSS.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1007/s12274-016-1401-6\",\n        \"dataset_ID\": 1530,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Singe-crystal microplates of two-dimensional organic-inorganic lead halide layered perovskites for optoelectronics\",\n        \"journal\": \"Nano Research\",\n        \"vol\": \"10\",\n        \"pages_start\": \"2117\",\n        \"pages_end\": \"2129\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HI, phenylethylamine, PbAc2\\u20223H2O, IPA\",\n        \"synthesis_product\": \"yellow crystals\",\n        \"synthesis_description\": \"First, PEAI was synthesized by adding HI (48 wt.% in water) to phenylethylamine at a molar ration of 1:1. This was performed at 0\\u00ba C. Water was evaporated in a hood (at ~100\\u00ba C) until PEAI crystals formed. Solution then cooled, powder product was filtered, washed with diethyl ether, and dried at 80\\u00ba C in a vacuum oven for ~24 hours.\\r\\nNext, (PEA)2PbI4 was synthesized. Fluoride-doped  tin oxide (FTO) glass substrate was coated with a film of lead acetate by drop-casting PbAc2\\u20223H2O (100 mg/mL). This was dried for 30 minutes at 60\\u00ba C. The PbAc2 film was placed into PEAI solution in IPA, having various concentrations at room temperature. The lead-coated side was facing down in the vial. After the reaction (~20 hrs), the substrate was removed, dipped into IPA again to remove extra solution, and dried under a stream of N2.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Single crystal was attached to tip of MiTeGen MicroMount, under a stream of N2 at 100 K. Data was recorded with Bruker Quazar SMART APEXII diffractometer with Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ja00006a076\",\n        \"dataset_ID\": 1531,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Preparation and Characterization of layered lead halide compounds\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"113\",\n        \"pages_start\": \"2328\",\n        \"pages_end\": \"2330\",\n        \"year\": \"1991\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"203.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"CCDC: 1186561\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.9b00247\",\n        \"dataset_ID\": 1533,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1888\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Longer Cations Increase Energetic Disorder in Excitonic 2D Hybrid Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1198\",\n        \"pages_end\": \"1205\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"HI (Sigma Aldrich, 57% w/w), chloroform (Fisher, HPLC grade), tributylphosphate (Acros Organics, 99+%), PbI2 (Strem, 99.999+%), phenylethylamine (PEA, Sigma-Aldrich, >99.5%), diethyl ether (Fisher, ACS grade, anhydrous, stabilized with BHT)\",\n        \"synthesis_product\": \"orange crystals\",\n        \"synthesis_description\": \"7 ml Unstabilized HI was treated with 10% v/v solution of tributylphosphate in chloroform. The aqueous phase (HI) was extracted.\\r\\nPbI2 (.231 g) was dissolved in the HI solution by heating to 100\\u00ba C under N2 flow. In it, 0.13 ml PEA is added. The reaction is then cooled to room temperature, at a constant rate of 2 \\u00baC/h. Then, the mixture is cooled at 4\\u00baC for 30 minutes, filtered, washed with diethyl ether, and dried overnight under vacuum at 50 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal X-Ray Diffraction\",\n        \"experimental_description\": \"SCXRD data are collected on a Bruker Kappa APEX II DUO diffractometer with a CCD area detector employing graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5). Crystals for SCXRD measured at 100 K are cooled by an Oxford Cryostream.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.jpclett.9b00247\",\n        \"dataset_ID\": 1534,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1889\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Longer Cations Increase Energetic Disorder in Excitonic 2D Hybrid Perovskites\",\n        \"journal\": \"The Journal of Physical Chemistry Letters\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1198\",\n        \"pages_end\": \"1205\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"HI (Sigma Aldrich, 57% w/w), chloroform (Fisher, HPLC grade), tributylphosphate (Acros Organics, 99+%), PbI2 (Strem, 99.999+%), phenylethylamine (PEA, Sigma-Aldrich, >99.5%), diethyl ether (Fisher, ACS grade, anhydrous, stabilized with BHT)\",\n        \"synthesis_product\": \"orange crystals\",\n        \"synthesis_description\": \"7 ml Unstabilized HI was treated with 10% v/v solution of tributylphosphate in chloroform. The aqueous phase (HI) was extracted. PbI2 (.231 g) was dissolved in the HI solution by heating to 100\\u00ba C under N2 flow. In it, 0.13 ml PEA is added. The reaction is then cooled to room temperature, at a constant rate of 2 \\u00baC/h. Then, the mixture is cooled at 4\\u00baC for 30 minutes, filtered, washed with diethyl ether, and dried overnight under vacuum at 50 \\u00b0C.\",\n        \"experimental_method\": \"Single crystal X-Ray Diffraction\",\n        \"experimental_description\": \"SCXRD data are collected on a Bruker Kappa APEX II DUO diffractometer with a CCD area detector employing graphite-monochromated Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5).\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.4947305\",\n        \"dataset_ID\": 1535,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"CRYSTAL09\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBESOL-D2\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"cc-p VDZ\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ab initio modeling of 2D layered organohalide lead perovskites\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"144\",\n        \"pages_start\": \"164701\",\n        \"pages_end\": \"164714\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/a\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1063/1.4947305\",\n        \"dataset_ID\": 1536,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Crystal09\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBESOL-D2\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"cc-p VDZ\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ab initio modeling of 2D layered organohalide lead perovskites\",\n        \"journal\": \"The Journal of Chemical Physics\",\n        \"vol\": \"144\",\n        \"pages_start\": \"164701\",\n        \"pages_end\": \"164714\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b05124\",\n        \"dataset_ID\": 1537,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"dielectric permittivity\",\n        \"primary_unit\": \"\\u03b5\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"High-Temperature Antiferroelectric of Lead Iodide Hybrid Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12470\",\n        \"pages_end\": \"12474\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbCO3 (2.67 g, 0.01 mol), CH3(CH2)3NH3I (1.34 g, 0.0067 mol), CH3CH2NH3I (1.15 g, 0.0067 mol)\",\n        \"synthesis_product\": \"FEP, AFEP, PEP\",\n        \"synthesis_description\": \"Lead iodide hybrid perovskites, (BA)2,(EA)2Pb3I10, were synthesized in a concentrated HI solution (40 mL, 57%) that contained PbCO3, CH3(CH2)3NH3I, CH3CH2NH3I.\",\n        \"experimental_method\": \"Temperature-cooling, Powder X-RAY Diffraction and Differential Scanning Calorimetry (DSC)\",\n        \"experimental_description\": \"Crystals of the hydroiodic solutions were obtained via a temperature- cooling method using differential scanning calorimetry (DSC) measurements with a heating/cooling rate of 10 K/min. The DSC traced reversible thermal peaks at 322/315 K (T1) and 363/360 K (T2) in the heating/cooling mode. The preparation of the HI solutions performed at  50\\u00b0C and kept at 4-6 \\u00b0C above its preliminary saturated temperature. The temperature was then slowly lowered with a cooling rate of 0.5 K/day, which resulted in bulk dark-red crystals. In addition, a bright yellow solution was obtained from heating the synthesis of compound 1 in an HI solution.  These crystals were then verified via powder X-ray diffraction at room temperature. The temperature dependence of the dielectric constant was measured using the double-wave method to\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1538,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"yellow crystals\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",\n        \"experimental_method\": \"single crystal X-ray diffraction\",\n        \"experimental_description\": \"SuperNova diffractometer with Mo K\\u03b1 radiation was used. Data was processed with Crystalclear software package, and the structures were solved by direct methods and refined with the SHELXLTL software package.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc21\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1539,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"yellow crystals\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",\n        \"experimental_method\": \"single crystal X-ray diffraction\",\n        \"experimental_description\": \"SuperNova diffractometer with Mo K\\u03b1 radiation was used. Data was processed with Crystalclear software package, and the structures were solved by direct methods and refined with the SHELXLTL software package.\",\n        \"physical_property\": \"330.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1540,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"two-photon absorption coefficient\",\n        \"primary_unit\": \"cm GW^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"yellow crystals\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",\n        \"experimental_method\": \"Two-photon Absorption Coefficient Measurements\",\n        \"experimental_description\": \"Z-scan apparatus was used to measure two-photon absorption property. The measurement was conducted with 350 fs pulses with a mode-locked fiber laser operating at 1030 nm and pulse repetition rate of 100 Hz.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1542,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"dielectric permittivity\",\n        \"primary_unit\": \"F/m\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"yellow crystals\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",\n        \"experimental_method\": \"Dielectric measurements\",\n        \"experimental_description\": \"Dielectric constants were obtained by using single crystal samples with silver conducting paste. Analyses were performed with TongHui TH2828 analyzer between 300-350 K.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"MHz\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1543,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"Film of thickness ~366 nm\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\\r\\n\\r\\nFilms were prepared by dissolving as-synthesized crystals at 500 mg/mL in dimethylformamide. The solutions are then spun onto wafers at 2500 rpm for 45 s, dried, and annealed at 80\\u00ba C for 15 min.\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"Measured at room temperature. A PE Lambda 900 UV-Visible spectrophotometer was used, and fluorescence measurements were collected with Edinbergh Analytical instrument FLS920.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1544,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"yellow crystals\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed.\",\n        \"experimental_method\": \"Thermogravimetric analysis\",\n        \"experimental_description\": \"Conducted with STA449C Thermal Analyzer, ranging from room temperature to 600\\u00ba C.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1545,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"Film of thickness ~366 nm\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed. \\r\\nFilms were prepared by dissolving as-synthesized crystals at 500 mg/mL in dimethylformamide. The solutions are then spun onto wafers at 2500 rpm for 45 s, dried, and annealed at 80\\u00ba C for 15 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Edinbergh Analytical instrument FLS920 was used to record the spectrum\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b04014\",\n        \"dataset_ID\": 1548,\n        \"id\": 391,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead bromide\",\n        \"formula\": \"(C4H9NH3)2(NH2CHNH2)Pb2Br7\",\n        \"group\": \"(BA)2(FA)Pb2Br7, bis(butylaminium) diaminomethanide septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, N2H5C\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanide lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bilayered Hybrid Perovskite Ferroelectric with Giant Two-Photon Absorption\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6809\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Pb(Ch3COO)2\\u20223H2O, HBr (40% w/w aqueous), formamidiniumacetate, butylamine\",\n        \"synthesis_product\": \"Film of thickness ~366 nm\",\n        \"synthesis_description\": \"First, Pb(Ch3COO)2\\u20223H2O (3.79 g, 10 mmol) was dissolved in 30 mL HBr by boiling and stirring. Then, formamidiniumacetate (0.512 g, 6.67 mmol) was added to the solution. This created a red precipitate, which soon dissolved under stirring. Butylamine (0.49 g, 6.67 mmol) was added to it, creating a yellow precipitate. This precipitate, too, dissolved under heating. Once the solution cooled to room temperature, crystals formed. Films were prepared by dissolving as-synthesized crystals at 500 mg/mL in dimethylformamide. The solutions are then spun onto wafers at 2500 rpm for 45 s, dried, and annealed at 80\\u00ba C for 15 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Edinbergh Analytical instrument FLS920 was used to record the spectrum\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1549,\n        \"id\": 392,\n        \"compound_name\": \"Guanidinium hypophosphite\",\n        \"formula\": \"C2H24Mn2N6O12P6\",\n        \"group\": \"[GUA]Mn(H2POO)3\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanaminium hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Magnetic Susceptibility\",\n        \"primary_unit\": \"X (emu/mol)\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco.\",\n        \"synthesis_product\": \"[GUA]Mn(H2POO)3\",\n        \"synthesis_description\": \"The solutions of manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution and the addition of alkylamine and alkylammonium dissolved into vapor diffusions provided pure samples of GUA and FA phases. In the acetone vapor-diffusion vial, single crystals of the monoclinic phase of [GUA]Mn(H2POO3) were produced as well as the triclinic phase of the compound from the DMSO vapor-diffusion. Although both phases crystallized, the sample was converted to the pure monoclinic phase via heating at 130 \\u00b0C for 2 hours.\",\n        \"experimental_method\": \"Quantum Design Magnetic Properties Measurement System (MPMS3)\",\n        \"experimental_description\": \"The magnetic susceptibility measurements of [GUA]Mn(H2POO)3 were calculated using MPMS3 and SQUID. [GUA]Mn(H2POO)3 was cooled to 1000 Oe in zero field mode. Since the temperature range was set to 2 to 300 K, only [GUA]Mn(H2POO)3 showed antiferromagnetic behavior, which gave a Neel temperature of 6.5K. The Curie-Weiss law was used to as a graphing technique to obtain the Weiss constants of both compounds. The Weiss constant of [GUA]Mn(H2POO)3 was measured to be -9.868 K with an effective magnetic moment of 6.12.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1550,\n        \"id\": 393,\n        \"compound_name\": \"Formamidinium hypophosphite\",\n        \"formula\": \"CH12MnN2O6P3\",\n        \"group\": \"[FA]Mn(H2POO)3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanide hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Magnetic Susceptibility\",\n        \"primary_unit\": \"X (emu/mol)\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco\",\n        \"synthesis_product\": \"[FA]Mn(H2POO)3\",\n        \"synthesis_description\": \"The solutions of manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution and the addition of alkylamine and alkylammonium dissolved into vapor diffusions provided pure samples of FA phases. Although both phases crystallized, the sample was converted to the pure monoclinic phase via heating at 130 \\u00b0C for 2 hours. The phase pure samples of [FA]Mn(H2POO3) were produced from the DMF vapor diffusion.\",\n        \"experimental_method\": \"Quantum Design Magnetic Properties Measurement System (MPMS3)\",\n        \"experimental_description\": \"he magnetic susceptibility measurements of [FA]Mn(H2POO3) were calculated using MPMS3 and SQUID. [FA]Mn(H2POO3) was cooled to 100 Oe in zero fields. The Curie-Weiss law was used to as a graphing technique to obtain the Weiss constants of both compounds. The Weiss constant of [FA]Mn(H2POO3) was found to be -5.766 K with an effective magnetic momentum of 5.02.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/n\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1551,\n        \"id\": 392,\n        \"compound_name\": \"Guanidinium hypophosphite\",\n        \"formula\": \"C2H24Mn2N6O12P6\",\n        \"group\": \"[GUA]Mn(H2POO)3\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanaminium hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"I2/m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1552,\n        \"id\": 392,\n        \"compound_name\": \"Guanidinium hypophosphite\",\n        \"formula\": \"C2H24Mn2N6O12P6\",\n        \"group\": \"[GUA]Mn(H2POO)3\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanaminium hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1553,\n        \"id\": 393,\n        \"compound_name\": \"Formamidinium hypophosphite\",\n        \"formula\": \"CH12MnN2O6P3\",\n        \"group\": \"[FA]Mn(H2POO)3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanide hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1554,\n        \"id\": 393,\n        \"compound_name\": \"Formamidinium hypophosphite\",\n        \"formula\": \"CH12MnN2O6P3\",\n        \"group\": \"[FA]Mn(H2POO)3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanide hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1555,\n        \"id\": 392,\n        \"compound_name\": \"Guanidinium hypophosphite\",\n        \"formula\": \"C2H24Mn2N6O12P6\",\n        \"group\": \"[GUA]Mn(H2POO)3\",\n        \"organic\": \"CH6N3\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanaminium hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"2\\u00d72\\u00d72\",\n        \"level_of_relativity\": \"non-collinear magnetism\",\n        \"basis_set_definition\": \"PAW (projector augmented wave) pseudopotentials and the wavefunction is expanded with a plane-wave basis set\",\n        \"numerical_accuracy\": \"+17 meV\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco.\",\n        \"synthesis_product\": \"[GUA]Mn(H2POO)3\",\n        \"synthesis_description\": \"ath sonication and magnetic stirring/heating at 50\\u00b0C was used to dissolved manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution (50% w/w; o.646 mL, 6 mmol). Then, alkylamine and alkylammonium sat (1 mmol) was added to the solution and stirred until it was dissolved. After dividing the solutions into 6 samples, each was dropped into various vapor diffusions that contained acetone, ethanol, N, N-dimethylacetamide (DMAC), N, N-dimethylformamide (DMF), or dimethyl sulfoxide (DMSO). Crystals were then obtained as acetone and ethanol diffused into the reactions, reducing the solubility of the solution as well as water increasing the concentration of the solvents at room temperature. The crystals observed were either colorless and small, indicating all phases present, or large with a pink color.\",\n        \"experimental_method\": \"TGA/DSC analysis\",\n        \"experimental_description\": \"An SDT instrument (simultaneous differential scanning calorimetry - thermogravimetric analysis (TGA)) was used to analyze the thermal stability of f [GUA]Mn(H2POO)3 and [FA]Mn(H2POO)3. These powder samples were heated to 600\\u00b0C at 20\\u00b0C/min under an argon flow of 100 ml/min.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"I2/m\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b09417\",\n        \"dataset_ID\": 1556,\n        \"id\": 393,\n        \"compound_name\": \"Formamidinium hypophosphite\",\n        \"formula\": \"CH12MnN2O6P3\",\n        \"group\": \"[FA]Mn(H2POO)3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"Mn(H2POO)3\",\n        \"iupac\": \"diaminomethanide hypophosphite\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"[Am]Mn(H2POO)3: A New Family of Hybrid Perovskites Based on the Hypophosphite Ligand\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"16999\",\n        \"pages_end\": \"17002\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Hypophosphorous acid, 50% w/w aq. soln., manganese carbonate, guanidine carbonate, formamidinium acetate, imidazole, 1,2,4-triazole, and dabco.\",\n        \"synthesis_product\": \"[FA]Mn(H2POO)3\",\n        \"synthesis_description\": \"Bath sonication and magnetic stirring/heating at 50\\u00b0C was used to dissolved manganese carbonate (0.115g, 1 mmol) in hypophosphorous acid solution (50% w/w; o.646 mL, 6 mmol). Then, alkylamine and alkylammonium sat (1 mmol) was added to the solution and stirred until it was dissolved. After dividing the solutions into 6 samples, each was dropped into various vapor diffusions that contained acetone, ethanol, N, N-dimethylacetamide (DMAC), N, N-dimethylformamide (DMF), or dimethyl sulfoxide (DMSO). Crystals were then obtained as acetone and ethanol diffused into the reactions, reducing the solubility of the solution as well as water increasing the concentration of the solvents at room temperature. The crystals observed were either colorless and small, indicating all phases present, or large with a pink color.\",\n        \"experimental_method\": \"TGA/DSC analysis\",\n        \"experimental_description\": \"An SDT instrument (simultaneous differential scanning calorimetry - thermogravimetric analysis (TGA)) was used to analyze the thermal stability of f [GUA]Mn(H2POO)3 and [FA]Mn(H2POO)3. These powder samples were heated to 600\\u00b0C at 20\\u00b0C/min under an argon flow of 100 ml/min.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.chemmater.8b01200\",\n        \"dataset_ID\": 1557,\n        \"id\": 288,\n        \"compound_name\": \"4-methylpiperidinium bismuth iodide: triiodide\",\n        \"formula\": \"(C6H14N)4I3BiI6\",\n        \"group\": \"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"I3BiI6, Iodide bismuth iodide\",\n        \"iupac\": \"tetrakis(4-methylpiperidinium) iodide bismuth iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Triiodide-Induced Band-Edge Reconstruction of a Lead-Free Perovskite-Derivative Hybrid for Strong Light Absorption\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"30\",\n        \"pages_start\": \"4081\",\n        \"pages_end\": \"4088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",\n        \"synthesis_product\": \"black needle-like crystals\",\n        \"synthesis_description\": \"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days. The crystals were redissolved in an oxidized HI solution, and the solution was again allowed to be evaporated over a few days.\",\n        \"experimental_method\": \"Thermogravimetric analysis\",\n        \"experimental_description\": \"The experiment was performed using a Netzsch TG 209 F1 Libra Thermo- Microbalance with alumina pans at a heating rate of 10 \\u00b0C/min.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.chemmater.8b01200\",\n        \"dataset_ID\": 1558,\n        \"id\": 288,\n        \"compound_name\": \"4-methylpiperidinium bismuth iodide: triiodide\",\n        \"formula\": \"(C6H14N)4I3BiI6\",\n        \"group\": \"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"I3BiI6, Iodide bismuth iodide\",\n        \"iupac\": \"tetrakis(4-methylpiperidinium) iodide bismuth iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Triiodide-Induced Band-Edge Reconstruction of a Lead-Free Perovskite-Derivative Hybrid for Strong Light Absorption\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"30\",\n        \"pages_start\": \"4081\",\n        \"pages_end\": \"4088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Differential scanning calorimetry measurements (DSC)\",\n        \"experimental_description\": \"A Netzsch TG 209 FI Libra Thermomirobalance system was used at a heating rate of 100 \\u00b0C/min was used to analyze the crystal samples (10 mg) thermogravimetric and differential thermal aspects.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.chemmater.8b01200\",\n        \"dataset_ID\": 1559,\n        \"id\": 288,\n        \"compound_name\": \"4-methylpiperidinium bismuth iodide: triiodide\",\n        \"formula\": \"(C6H14N)4I3BiI6\",\n        \"group\": \"MP-T-BiI6, tetrakis(4-methylpiperidinium) iodide hexaiodobismuthate(III)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"I3BiI6, Iodide bismuth iodide\",\n        \"iupac\": \"tetrakis(4-methylpiperidinium) iodide bismuth iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Triiodide-Induced Band-Edge Reconstruction of a Lead-Free Perovskite-Derivative Hybrid for Strong Light Absorption\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"30\",\n        \"pages_start\": \"4081\",\n        \"pages_end\": \"4088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",\n        \"synthesis_product\": \"black needle-like crystals\",\n        \"synthesis_description\": \"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days. The crystals were redissolved in an oxidized HI solution, and the solution was again allowed to be evaporated over a few days.\",\n        \"experimental_method\": \"UV-vis absorbance (diffuse reflectance)\",\n        \"experimental_description\": \"The reflectance spectrum was collected using a LAMBDA 950 UV/vis spectrophotometer. Reflectance was converted to absorbance using the Kubelka\\u2013Munk function.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.chemmater.8b01200\",\n        \"dataset_ID\": 1560,\n        \"id\": 394,\n        \"compound_name\": \"4-methylpiperidinium bismuth iodide\",\n        \"formula\": \"(C6H14N)3Bi2I9\",\n        \"group\": \"MP-Bi2I9, tris(4-methylpiperidinium) nonaiodo dibismuthate(III)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"tris(4-methylpiperidinium) bismuth iodide\",\n        \"last_update\": \"2022-07-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Triiodide-Induced Band-Edge Reconstruction of a Lead-Free Perovskite-Derivative Hybrid for Strong Light Absorption\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"30\",\n        \"pages_start\": \"4081\",\n        \"pages_end\": \"4088\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"4-methylpiperidine, Bi2O3, HI (47 wt.%)\",\n        \"synthesis_product\": \"red needle-like crystals\",\n        \"synthesis_description\": \"4-methylpiperidine (0.99 g, 10 mmol) and Bi2O3 (1.16 g, 2.5 mmol) were mixed in 30 mL of HI. The solution was left at room temperature to be evaporated. The crystals formed after several days.\",\n        \"experimental_method\": \"UV-vis absorbance (diffuse reflectance)\",\n        \"experimental_description\": \"The reflectance spectrum was collected using a LAMBDA 950 UV/vis spectrophotometer. Reflectance was converted to absorbance using the Kubelka\\u2013Munk function.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.5b01896\",\n        \"dataset_ID\": 1561,\n        \"id\": 398,\n        \"compound_name\": \"Bis(methylammonium) copper bromide chloride\",\n        \"formula\": \"(CH3NH3)2CuCl2Br2\",\n        \"group\": \"MA2CuCl2Br2, bis(methanaminium) dibromo dichlorocuprate(II)\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"CuCl2Br2, Copper bromide chloride\",\n        \"iupac\": \"bis(methanaminium) copper bromide chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead-Free MA2CuClxBr4-x Hybrid Perovskites\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"55\",\n        \"pages_start\": \"1044\",\n        \"pages_end\": \"1052\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water), Hydrobromic acid (48% in water, Sigma-Aldrich), CuCl2 (copper chloride, 99% Sigma-Aldrich), CuBr2 (copper bromide, 99% Sigma-Aldrich)\",\n        \"synthesis_product\": \"MA2CuCl2Br2\",\n        \"synthesis_description\": \"MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl.\\r\\nMABr was synthesized by reacting 18 mL of methylamine solution with 8 mL of HBr.\\r\\n\\r\\nThe precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"2950 TGA HR V5.4 (TA Instruments) was used for the TGA analysis under nitrogen flow (40 mL/min).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.5b01896\",\n        \"dataset_ID\": 1562,\n        \"id\": 399,\n        \"compound_name\": \"Bis(methylammonium) copper bromide chloride\",\n        \"formula\": \"(CH3NH3)2CuCl0.5Br3.5\",\n        \"group\": \"MA2CuCl0.5Br3.5, tetrakis(methanaminium) septabromo monochloro diplumbate(II)\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"CuCl0.5Br3.5, Copper chloride bromide\",\n        \"iupac\": \"bis(methanaminium) copper bromide chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead-Free MA2CuClxBr4-x Hybrid Perovskites\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"55\",\n        \"pages_start\": \"1044\",\n        \"pages_end\": \"1052\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water), Hydrobromic acid (48% in water, Sigma-Aldrich), CuCl2 (copper chloride, 99% Sigma-Aldrich), CuBr2 (copper bromide, 99% Sigma-Aldrich)\",\n        \"synthesis_product\": \"MA2CuCl0.5Br3.5\",\n        \"synthesis_description\": \"MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl. MABr was synthesized by reacting 18 mL of methylamine solution with 8 mL of HBr. The precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"2950 TGA HR V5.4 (TA Instruments) was used for the TGA analysis under nitrogen flow (40 mL/min).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.5b01896\",\n        \"dataset_ID\": 1563,\n        \"id\": 400,\n        \"compound_name\": \"Methylammonium copper chloride\",\n        \"formula\": \"(CH3NH3)2CuCl4\",\n        \"group\": \"bis(methanaminium) tetrachlorocuprate\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead-Free MA2CuClxBr4-x Hybrid Perovskites\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"55\",\n        \"pages_start\": \"1044\",\n        \"pages_end\": \"1052\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water),  CuCl2 (copper chloride, 99% Sigma-Aldrich), DMSO\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl. The precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h.\\r\\nThe obtained powder was dissolved in DMSO to prepare a 1 M solution. The solution was spin-coated on glass slides.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"UV3600, Shimadzu was used to record the spectra\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"298K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.5b01896\",\n        \"dataset_ID\": 1564,\n        \"id\": 401,\n        \"compound_name\": \"Bis(methylammonium) copper bromide chloride\",\n        \"formula\": \"(CH3NH3)2CuClBr3\",\n        \"group\": \"MA2CuClBr3, bis(methanaminium) tribromo monochlorocuprate(II)\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"CuClBr3, Copper chloride bromide\",\n        \"iupac\": \"bis(methanaminium) copper bromide chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lead-Free MA2CuClxBr4-x Hybrid Perovskites\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"55\",\n        \"pages_start\": \"1044\",\n        \"pages_end\": \"1052\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"methylamine solution (CH3NH2, 40% in methanol), Hydrochloric acid (37 wt % in water), Hydrobromic acid (48% in water, Sigma-Aldrich), CuCl2 (copper chloride, 99% Sigma-Aldrich), CuBr2 (copper bromide, 99% Sigma-Aldrich), DMSO\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"MACl was synthesized by reacting 16.7 mL of methylamine solution with 11.3 mL of HCl. MABr was synthesized by reacting 18 mL of methylamine solution with 8 mL of HBr. The precursors in required molar ratios according to the stoichiometry were mixed in 100 mL EtOH by heating and stirring at 60 degrees Celsius for 2 h. The solution was left overnight in an ice bath. The obtained crystals were filtered and dried at 60 degrees Celsius in a vacuum oven for 12 h. The obtained powder was dissolved in DMSO to prepare a 1 M solution. The solution was spin-coated on glass slides.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"UV3600, Shimadzu was used to record the spectra\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"298K\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsaem.9b00419\",\n        \"dataset_ID\": 1566,\n        \"id\": 402,\n        \"compound_name\": \"Azetidinium methylammonium lead bromide\",\n        \"formula\": \"C3H8Br3NPb\",\n        \"group\": \"Azetidinium lead bromide, Az0.4MA0.6PbBr3, azetidinium methanaminium tribromoplumbate(II)\",\n        \"organic\": \"C3H8N\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"azetidinium methanaminium lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stable 6H Organic\\u2013Inorganic Hybrid Lead Perovskite and Competitive Formation of 6H and 3C Perovskite Structure with Mixed A Cations\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"8\",\n        \"pages_start\": \"5427\",\n        \"pages_end\": \"5437\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AzCl, NaBr, DMF/DMSO\",\n        \"synthesis_product\": \"Az0.4MA0.6PbBr3\",\n        \"synthesis_description\": \"Ion exchanged between AzCl and NaBr was performed to yield AzBr, which was then later dried in DMF/DMSO (4:1) solvents with PbBr2 to produce Az0.4MA0.6PbBr3. The crystals were obtained via slow diffusion of the antisolvent chloroform, which was dissolved in DMF.\",\n        \"experimental_method\": \"Absorbance spectra\",\n        \"experimental_description\": \"Using the UV-VIS spectrometer, the absorption for AzPbBr3 ( single crystal) and MAPbBr3 powders were obtained. The absorption spectra were recorded using a JASCO-V650 double beam spectrophotometer and the bandgap was determined using the Band-Gap Calculation program in the spectrophotometer. The spectroscopy data were collected over the frequency of 100 Hz, an excitation of 100 mV, collected at 2 K increments at a heating/cooling rate of 1 K min-1 between 50 and 473 K, and used a closed cycle cryocooler.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"Sample 1\",\n        \"space_group\": \"P63/mmc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.0c00371\",\n        \"dataset_ID\": 1567,\n        \"id\": 310,\n        \"compound_name\": \"3-fluoropiperidinium lead iodide\",\n        \"formula\": \"(C5H11FN)PbI3\",\n        \"group\": \"(3-FPD)PbI3, (3- fluoropiperidinium)PbI3, 3-fluoropiperidinium triiodoplumbate(II)\",\n        \"organic\": \"C5H11FN\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"3-fluoropiperidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observation of Vortex Domains in a Two-Dimensional Lead Iodide Perovskite Ferroelectric\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"4952\",\n        \"pages_end\": \"4931\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, 3-fluoropiperidinium hydrochloride, HI (47 wt % in water)\",\n        \"synthesis_product\": \"yellow block-like crystals\",\n        \"synthesis_description\": \"PbI2 (0.92 g, 2 mmol) and 3-fluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.0c00371\",\n        \"dataset_ID\": 1568,\n        \"id\": 309,\n        \"compound_name\": \"4-fluoropiperidinium lead iodide\",\n        \"formula\": \"(C5H11FN)PbI3\",\n        \"group\": \"(4-FPD)PbI3, (4-fluoropiperidinium)PbI3, 4-fluoropiperidinium triiodoplumbate(II)\",\n        \"organic\": \"C5H11FN\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"4-fluoropiperidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observation of Vortex Domains in a Two-Dimensional Lead Iodide Perovskite Ferroelectric\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"4952\",\n        \"pages_end\": \"4931\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, 4-fluoropiperidinium hydrochloride, HI (47 wt % in water)\",\n        \"synthesis_product\": \"yellow prismatic crystals\",\n        \"synthesis_description\": \"PbI2 (0.92 g, 2 mmol) and 4-fluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.0c00371\",\n        \"dataset_ID\": 1569,\n        \"id\": 308,\n        \"compound_name\": \"Piperidinium lead iodide\",\n        \"formula\": \"(C5H12N)PbI3\",\n        \"group\": \"(piperidinium)PbI3, (PD)PbI3, piperidinium triiodoplumbate(II)\",\n        \"organic\": \"C5H12N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"piperidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observation of Vortex Domains in a Two-Dimensional Lead Iodide Perovskite Ferroelectric\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"4952\",\n        \"pages_end\": \"4931\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, piperidinium hydrochloride, HI (47 wt % in water)\",\n        \"synthesis_product\": \"yellow prismatic crystals\",\n        \"synthesis_description\": \"PbI2 (0.92 g, 2 mmol) and piperidinium hydrochloride (0.63 g, 2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",\n        \"experimental_method\": \"Thermogravimetric analysis\",\n        \"experimental_description\": \"Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.0c00371\",\n        \"dataset_ID\": 1570,\n        \"id\": 307,\n        \"compound_name\": \"Bisdecakis(3,3-difluoropiperidinium) lead iodide\",\n        \"formula\": \"C60H120F24N12Pb7I26\",\n        \"group\": \"(3,3-difluoropiperidinium)12Pb7I26, (3,3-DFPD)12Pb7I26, bisdecakis(3,3-difluoropiperidinium) hexaicosiodo septaplumbate(II)\",\n        \"organic\": \"C60H120F24N12\",\n        \"inorganic\": \"Pb7I26, Lead iodide\",\n        \"iupac\": \"bisdecakis(3,3-difluoropiperidinium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observation of Vortex Domains in a Two-Dimensional Lead Iodide Perovskite Ferroelectric\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"4952\",\n        \"pages_end\": \"4931\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, 3,3-difluoropiperidinium hydrochloride, HI (47 wt % in water)\",\n        \"synthesis_product\": \"yellow prismatic crystals\",\n        \"synthesis_description\": \"PbI2 (0.92 g, 2 mmol) and 3,3-difluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.0c00371\",\n        \"dataset_ID\": 1572,\n        \"id\": 306,\n        \"compound_name\": \"Bis(4,4-difluoropiperidinium) lead iodide\",\n        \"formula\": \"(C5H10F2N)2PbI4\",\n        \"group\": \"(4,4-difluoropiperidinium)2PbI4, (4,4-DFPD)2PbI4, bis(4,4-difluoropiperidinium) tetraiodoplumbate(II)\",\n        \"organic\": \"C5H10F2N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(4,4-difluoropiperidinium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observation of Vortex Domains in a Two-Dimensional Lead Iodide Perovskite Ferroelectric\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"4952\",\n        \"pages_end\": \"4931\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, 4,4-difluoropiperidinium hydrochloride, HI (47 wt % in water)\",\n        \"synthesis_product\": \"Red plate-like crystals\",\n        \"synthesis_description\": \"PbI2 (0.92 g, 2 mmol) and 4,4-difluoropiperidinium hydrochloride (2 mmol) were mixed in 20 mL HI solution. The precipitate was dissolved by heating at 443 K. Slow cooling of the solution resulted in the formation of the crystals.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"Data were recorded using a NETZSCH TG 209F3 apparatus under N2 atmosphere\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.201501978\",\n        \"dataset_ID\": 1573,\n        \"id\": 403,\n        \"compound_name\": \"Methylammonium bismuth iodide\",\n        \"formula\": \"CH3NH3Bi2I9\",\n        \"group\": \"Tris(methanaminium) nonaiodo dibismuthate(III)\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"methylaminium bismuth iodide\",\n        \"last_update\": \"2022-08-22\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bismuth Based Hybrid Perovskites A3Bi2I9 (A: Methylammonium or Cesium) for Solar Cell Application\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"27\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6813\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"CH3NH3I, BiI3\",\n        \"synthesis_product\": \"MA3Bi2I9 film\",\n        \"synthesis_description\": \"A mixture of CH3NH3I (2.475 M) and BiI3 (1.65 M) in dimethylformamide (DMF)/dimethyl sulfoxide (DMSO) solvent mixture (7/3 by volume) was used to synthesize MA3Bi2I9. The solution was spin-coated onto TiO 2 / glass substrate at 1500 rpm for 20 s, followed by annealing on a hot plate at 110 \\u00b0C for 30 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using Fluorolog-3 instrument (Horiba Jobin Yvon).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.201501978\",\n        \"dataset_ID\": 1575,\n        \"id\": 404,\n        \"compound_name\": \"Cesium bismuth iodide\",\n        \"formula\": \"CH3NH3Bi2I9\",\n        \"group\": \"Tricesium nonaiodo dibismuthate(II)\",\n        \"organic\": \"CH3NH3\",\n        \"inorganic\": \"Bi2I9, Bismuth iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-22\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bismuth Based Hybrid Perovskites A3Bi2I9 (A: Methylammonium or Cesium) for Solar Cell Application\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"27\",\n        \"pages_start\": \"6806\",\n        \"pages_end\": \"6813\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"CsI, BiI3\",\n        \"synthesis_product\": \"Cs3Bi2I9 film\",\n        \"synthesis_description\": \"A mixture of Cs(2.475 M) and BiI3 (1.65 M) in dimethylformamide (DMF)/dimethyl sulfoxide (DMSO) solvent mixture (7/3 by volume) was used to synthesize Cs3Bi2I9. The solution was spin-coated onto TiO 2 / glass substrate at 1500 rpm for 20 s, followed by annealing on a hot plate at 110 \\u00b0C for 30 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"The spectrum was recorded using Fluorolog-3 instrument (Horiba Jobin Yvon).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P63/ mmc\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.jpclett.6b00793\",\n        \"dataset_ID\": 1576,\n        \"id\": 47,\n        \"compound_name\": \"N-methylethane-1,2-diammonium lead bromide\",\n        \"formula\": \"C3H12N2PbBr4\",\n        \"group\": \"N-methylethane-1,2-diaminium tetrabromoplumbate(II), (N-MEDA)PbBr4, C3N2H12PbBr4\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N-methylethane-1,2-diaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"time\",\n        \"secondary_unit\": \"ns\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Mechanism for Broadband White-Light Emission from Two-Dimensional (110) Hybrid Perovskites\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"12\",\n        \"pages_start\": \"2258\",\n        \"pages_end\": \"2263\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"N,N-dimethylformamide\",\n        \"synthesis_product\": \"(N-MEDA)[PbBr4]\",\n        \"synthesis_description\": \"Films of (N-MEDA)[PbBr4] were produced by dissolved 0.1 M of (N-MEDA)[PbBr4] in an N, N-dimethylformamide via starting at 3000 rpm. Single crystals were yielded from annealing the solution at 100 \\u00b0C for 10 minutes. Depressing ball-milled powder at a pressure of 10,000-15,000 psi produced the pellet samples.\",\n        \"experimental_method\": \"Time-Correlated Single Photon Counting (TCSPC) measurement\",\n        \"experimental_description\": \"A fiber laser tripled from a wavelength range of 1030 nm to 343 nm was used to excite a single crystal pellet sample of  (N-MEDA)[PbBr4]. The TCSPC system was set at a pulse duration of 500-f and a repetition rate of 1.28-MHz. A  hybrid photomultiplier detector assembly was used to observe the PL intensity via  fluorescence bandpass filters and  reflective neutral density\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"Powder-pressed Pellet\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.6b08175\",\n        \"dataset_ID\": 1577,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Direct Observation of Electron\\u2013Phonon Coupling and Slow Vibrational Relaxation in Organic\\u2013Inorganic Hybrid Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"42\",\n        \"pages_start\": \"13798\",\n        \"pages_end\": \"13801\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Phenethylammonium lead iodide (PEALI) crystals, anhydrous acetonitrile (Acros Organics), sapphire substrates (Rayotek Scientific)\",\n        \"synthesis_product\": \"Phenethylammonium lead iodide films\",\n        \"synthesis_description\": \"PEALI crystals are dissolved by sonication in anhydrous acetonitrile at a concentration of 15 mg/mL. The solution is filtered through a 0.2 \\u00b5m PTFE syringe filter (Pall Corporation) and spun on cleaned sapphire substrates by ramping the spin rate over 2 s to 2500 rpm and spinning for 10 s. After spin-casting, the films are annealed for 10 min at 80 \\u02daC. The entire process is carried out in a nitrogen-filled glove box.\",\n        \"experimental_method\": \"UV-VIS Absorption\",\n        \"experimental_description\": \"The absorption spectra measurements of PEALI thin films were obtained by using Agilent Cary 5000 spectrophotometer.\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"---\",\n        \"dataset_ID\": 1578,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"---\",\n        \"vol\": \"---\",\n        \"pages_start\": \"---\",\n        \"pages_end\": \"---\",\n        \"year\": \"---\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Received from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.1700704\",\n        \"dataset_ID\": 1579,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"Quantum Espresso\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"6x6x1\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"ultra-soft pseudopotentials\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Giant Rashba splitting in 2D organic-inorganic halide perovskites measured by transient spectroscopies\",\n        \"journal\": \"SCIENCE ADVANCES\",\n        \"vol\": \"3\",\n        \"pages_start\": \"e1700704\",\n        \"pages_end\": \"e1700704\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Retrieved from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1583,\n        \"id\": 405,\n        \"compound_name\": \"S-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"S-NEA2PbBr4, S-1-(1-naphthyl)ethanaminium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"S-1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1629,\n            1630,\n            1864\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"S-1-(1-naphthyl)ethylamine, PbBr2\",\n        \"synthesis_product\": \"S-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"synthesis_description\": \"A hot solution of PbBr2 (45 mg, 0.12 mmol) and S-1-(1-naphthyl)ethylamine (39 \\u00b5L, 0.24 mmol ) in 0.5 ml aq. HBr and 1.2 ml deionized water in a sealed vial with an N2 atmosphere was slowly cooled from 95 \\u00b0C to room temperature over 48 hr. The colorless, plate-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1584,\n        \"id\": 406,\n        \"compound_name\": \"R-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"R-NEA2PbBr4, R-1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"R-1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"R-1-(1-naphthyl)ethylamine, PbBr2\",\n        \"synthesis_product\": \"R-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"synthesis_description\": \"A hot solution of PbBr2 (45 mg, 0.12 mmol) and R-1-(1-naphthyl)ethylamine (39 \\u00b5L, 0.24 mmol ) in 0.5 ml aq. HBr and 1.2 ml deionized water in a sealed vial with an N2 atmosphere was slowly cooled from 95 \\u00b0C to room temperature over 48 hr. The colorless, plate-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1585,\n        \"id\": 407,\n        \"compound_name\": \"S-1-methyl benzylamine lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"S-MBA2PbI4, S-MBPI, (S)-\\u0152\\u00b1-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"S-1-methyl benzylaminium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-\\u03b1-methyl benzylamine, PbI2\",\n        \"synthesis_product\": \"(S)-(\\u2212)-\\u03b1-methyl benzylammonium lead iodide (S-MBA2PbI4)\",\n        \"synthesis_description\": \"Single crystals of S-MBPI were grown by slowly evaporating a solution of (S)-(\\u2212)-\\u03b1-methyl benzylamine (25 \\u00b5L, 0.2 mmol) and PbI2 (45 mg, 0.1 mmol) in 1 ml aq. HI and 1 ml methanol at room temperature under N2 atmosphere. The orange-red, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P212121\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1586,\n        \"id\": 407,\n        \"compound_name\": \"S-1-methyl benzylamine lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"S-MBA2PbI4, S-MBPI, (S)-\\u0152\\u00b1-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"S-1-methyl benzylaminium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-\\u03b1-methyl benzylamine, PbI2\",\n        \"synthesis_product\": \"(S)-(\\u2212)-\\u03b1-methyl benzylammonium lead iodide (S-MBA2PbI4)\",\n        \"synthesis_description\": \"Single crystals of S-MBPI were grown by slowly evaporating a solution of (S)-(\\u2212)-\\u03b1-methyl benzylamine (25 \\u00b5L, 0.2 mmol) and PbI2 (45 mg, 0.1 mmol) in 1 ml aq. HI and 1 ml methanol at room temperature under N2 atmosphere. The orange-red, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 200 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"200.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P212121\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1587,\n        \"id\": 407,\n        \"compound_name\": \"S-1-methyl benzylamine lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"S-MBA2PbI4, S-MBPI, (S)-\\u0152\\u00b1-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"S-1-methyl benzylaminium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-\\u03b1-methyl benzylamine, PbI2\",\n        \"synthesis_product\": \"(S)-(\\u2212)-\\u03b1-methyl benzylammonium lead iodide (S-MBA2PbI4)\",\n        \"synthesis_description\": \"Single crystals of S-MBPI were grown by slowly evaporating a solution of (S)-(\\u2212)-\\u03b1-methyl benzylamine (25 \\u00b5L, 0.2 mmol) and PbI2 (45 mg, 0.1 mmol) in 1 ml aq. HI and 1 ml methanol at room temperature under N2 atmosphere. The orange-red, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 100 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P212121\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1588,\n        \"id\": 408,\n        \"compound_name\": \"1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"1-(1-naphthyl)ethylamine (98%), PbBr2\",\n        \"synthesis_product\": \"1-(1-naphthyl)ethylammoium lead bromide\",\n        \"synthesis_description\": \"A hot solution of 1-(1-naphthyl)ethylamine (39 \\u00b5L, 0.24 mmol ) and PbBr2 (45 mg, 0.12 mmol) in 0.5 ml of aq. HBr and 1.2 ml methanol is cooled from 95 \\u00b0C to room temperature over 48 hr. The colorless plate-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Bruker APEX II CCD diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and X-ray tube operating at 50 kV and 30 mA\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1589,\n        \"id\": 409,\n        \"compound_name\": \"S-1-(1-naphthyl)ethylammonium lead iodide\",\n        \"formula\": \"C24H28N2Pb2I6\",\n        \"group\": \"S-NEA2Pb2I6, S-C24H28N2Pb2I6, S-NPI, S-1-(1-naphthyl)ethylammonium hexaiodo diplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"S-1-(1-naphthyl)ethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"1D Face-sharing metal halide hybrid\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-1-(1-naphthyl)ethylamine (\\u226599%), PbI2\",\n        \"synthesis_product\": \"S-NEA2Pb2I6 (S-NPI)\",\n        \"synthesis_description\": \"Single crystals of 1D S-NEA2Pb2I6 (S-NPI) were obtained by cooling a hot aq. HI solution of S-1-(1-naphthyl)ethylamine (0.25 mmol) and PbI2 (0.125 mmol) from  90 \\u00b0C to room-temperature in 48 hr. The pale-yellow, needle-like crystals were filtered, washed with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Bruker APEX II CCD diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and X-ray tube operating at 50 kV and 30 mA\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P212121\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1608,\n        \"id\": 410,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead bromide\",\n        \"formula\": \"(C6H14N)2PbBr4\",\n        \"group\": \"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cyclohexylammonium bromide, PbBr2, HBr\",\n        \"synthesis_product\": \"large, pale-yellow crystals\",\n        \"synthesis_description\": \"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc21\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1609,\n        \"id\": 410,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead bromide\",\n        \"formula\": \"(C6H14N)2PbBr4\",\n        \"group\": \"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cyclohexylammonium bromide, PbBr2, HBr\",\n        \"synthesis_product\": \"large, pale-yellow crystals\",\n        \"synthesis_description\": \"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"383.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1610,\n        \"id\": 410,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead bromide\",\n        \"formula\": \"(C6H14N)2PbBr4\",\n        \"group\": \"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"dielectric permittivity\",\n        \"primary_unit\": \"abs. units\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cyclohexylammonium bromide, PbBr2, HBr\",\n        \"synthesis_product\": \"large, pale-yellow crystals\",\n        \"synthesis_description\": \"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"Physical Properties Measurement\",\n        \"experimental_description\": \"Measured with precision impedance analyzer (Model: Agilent 4294A, Santa Clara, CA). Measured at 1 MHz.\",\n        \"physical_property\": \"1.0\",\n        \"unit\": \"MHz\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1611,\n        \"id\": 410,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead bromide\",\n        \"formula\": \"(C6H14N)2PbBr4\",\n        \"group\": \"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cyclohexylammonium bromide, PbBr2, HBr\",\n        \"synthesis_product\": \"large, pale-yellow crystals\",\n        \"synthesis_description\": \"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1612,\n        \"id\": 410,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead bromide\",\n        \"formula\": \"(C6H14N)2PbBr4\",\n        \"group\": \"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"CASTEP Program\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA-PBE\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Norm-conserving pseudopotential\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cyclohexylammonium bromide, PbBr2, HBr\",\n        \"synthesis_product\": \"large, pale-yellow crystals\",\n        \"synthesis_description\": \"First, CHA was synthesized by mixing Cyclohexylammonium bromide (20 mmol, 3.60 g), PbBr2 (10 mmol, 3.67 g) and HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Finally, large, pale yellow crystals of (CHA)2PbBr3 were obtained by cooling the solution at a rate of 0.125 K/h\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1613,\n        \"id\": 410,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead bromide\",\n        \"formula\": \"(C6H14N)2PbBr4\",\n        \"group\": \"(CHA)2PbBr4, bis(cyclohexylaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cyclohexylammonium bromide, PbBr2, HBr\",\n        \"synthesis_product\": \"large, pale-yellow crystals\",\n        \"synthesis_description\": \"Cyclohexylammonium bromide (20 mmol, 3.60 g), and PbBr2 (10 mmol, 3.67 g) were dissolved in HBr aqueous solution (40%, 100 mL). A clear solution resulted after refluxing the mixture at 353 K for 3 hrs. Crystals of (CHA)2PbBr4 were obtained by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1614,\n        \"id\": 411,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead iodide\",\n        \"formula\": \"(C6H14N)2PbI4\",\n        \"group\": \"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, PbI2, HI\",\n        \"synthesis_product\": \"Large, orange crystals\",\n        \"synthesis_description\": \"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1615,\n        \"id\": 411,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead iodide\",\n        \"formula\": \"(C6H14N)2PbI4\",\n        \"group\": \"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, PbI2, HI\",\n        \"synthesis_product\": \"Large, orange crystals\",\n        \"synthesis_description\": \"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"463.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmca\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1616,\n        \"id\": 411,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead iodide\",\n        \"formula\": \"(C6H14N)2PbI4\",\n        \"group\": \"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, PbI2, HI\",\n        \"synthesis_product\": \"Large, orange crystals\",\n        \"synthesis_description\": \"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1617,\n        \"id\": 411,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead iodide\",\n        \"formula\": \"(C6H14N)2PbI4\",\n        \"group\": \"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"CASTEP Program\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA-PBE\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Norm-conserving pseudopotential\",\n        \"numerical_accuracy\": \"energy cutoff: 820 eV\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, PbI2, HI\",\n        \"synthesis_product\": \"Large, orange crystals\",\n        \"synthesis_description\": \"First, cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals soon grew by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201505224\",\n        \"dataset_ID\": 1618,\n        \"id\": 411,\n        \"compound_name\": \"Bis(cyclohexylammonium) lead iodide\",\n        \"formula\": \"(C6H14N)2PbI4\",\n        \"group\": \"(CHA)2PbI4, bis(cyclohexylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C6H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(cyclohexylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Bandgap Engineering of Lead\\u2010Halide Perovskite\\u2010Type Ferroelectrics\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2579\",\n        \"pages_end\": \"2586\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"cyclohexylamine, PbI2, HI\",\n        \"synthesis_product\": \"Large, orange crystals\",\n        \"synthesis_description\": \"cyclohexylamine (10 mmol, 0.99 g) and PbI2 (5 mmol, 2.31 g) were mixed in HI aqueous solution (45%, 60 mL). The resulting precipitate dissolved after the solution was refluxed for 4 hours at 363 K. Large crystals were grown by cooling the solution at a rate of 0.125 K/h.\",\n        \"experimental_method\": \"UV-vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1621,\n        \"id\": 408,\n        \"compound_name\": \"1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"2\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1629,\n        \"id\": 405,\n        \"compound_name\": \"S-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"S-NEA2PbBr4, S-1-(1-naphthyl)ethanaminium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"S-1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1583,\n            1630,\n            1864\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"2\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1630,\n        \"id\": 405,\n        \"compound_name\": \"S-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"S-NEA2PbBr4, S-1-(1-naphthyl)ethanaminium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"S-1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1583,\n            1629,\n            1864\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06\",\n        \"k_point_grid\": \"3\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA with SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1631,\n        \"id\": 406,\n        \"compound_name\": \"R-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"R-NEA2PbBr4, R-1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"R-1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1632\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"2\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1632,\n        \"id\": 406,\n        \"compound_name\": \"R-1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"R-NEA2PbBr4, R-1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"R-1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1631\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06\",\n        \"k_point_grid\": \"3\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA with SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1633,\n        \"id\": 408,\n        \"compound_name\": \"1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1634\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"2\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1634,\n        \"id\": 408,\n        \"compound_name\": \"1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1633\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06\",\n        \"k_point_grid\": \"3\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA with SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1635,\n        \"id\": 407,\n        \"compound_name\": \"S-1-methyl benzylamine lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"S-MBA2PbI4, S-MBPI, (S)-\\u0152\\u00b1-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"S-1-methyl benzylaminium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1636\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"2\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-020-18485-7\",\n        \"dataset_ID\": 1636,\n        \"id\": 407,\n        \"compound_name\": \"S-1-methyl benzylamine lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"S-MBA2PbI4, S-MBPI, (S)-\\u0152\\u00b1-methyl benzylamine lead iodide, S-1-methyl benzylaminium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"S-1-methyl benzylaminium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1635\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE06\",\n        \"k_point_grid\": \"3\\u00d74\\u00d74\",\n        \"level_of_relativity\": \"atomic ZORA with SOC\",\n        \"basis_set_definition\": \"NAO\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Organic-to-inorganic structural chirality transfer in a 2D hybrid perovskite and impact on Rashba-Dresselhaus spin-orbit coupling.\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4699-1\",\n        \"pages_end\": \"4699-10\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0261474\",\n        \"dataset_ID\": 1637,\n        \"id\": 412,\n        \"compound_name\": \"Bis(2-bromophenethyl)ammonium tin iodide\",\n        \"formula\": \"(2-BrC6H4C2H4NH3)2SnI4\",\n        \"group\": \"(2-BrPEA)2SnI4, bis(2-bromophenethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"BrC6H4C2H4NH3\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(2-bromophenethanaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Perovskites (2-XC6H4C2H4NH3)2SnI4 (X = F, Cl, Br): Steric Interaction between the Organic and Inorganic Layers\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"2031\",\n        \"pages_end\": \"2039\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"SnI2, 2-BrC6H4C2H4NH3I, CH3OH, C6H5CH3\",\n        \"synthesis_product\": \"platelike, bright red crystals\",\n        \"synthesis_description\": \"Growing the crystal through the slow evaporation of methanol/toluene mixed solution dissolving the organic and inorganic salts. Adding 45.5 mg (0.122 mmol) SnI2 and 80.0 mg (0.244 mmol) (2-bromophenethyl)ammonium iodide into a vial under an inert atmosphere. Then 1.0 mL of anhydrous methanol is added to dissolve the mixture to form a yellow solution. Filtering the solution through a Teflon filter (pore size:\\u2009 0.2 \\u03bcm) and adding 2.0 mL of anhydrous toluene into the solution. The vial is loosely capped and placed for 3 days for the formation of platelike, bright red crystals (120 mg, yield 95%) during the slow cooling process.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Selecting a blocklike crystal under a microscope and attaching it to the end of a quartz fiber with 5 min epoxy. Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo K\\u03b1 radiation), is utilized to collect a full sphere of data at room temperature. A detector distance of approximately 5.0 cm and collection in 2272 frames with increasing \\u03c9 is applied for obtaining intensity data. Using Shelxl 97 to solve and refine the crystal structure.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/ic0261474\",\n        \"dataset_ID\": 1638,\n        \"id\": 413,\n        \"compound_name\": \"Bis(2-chlorophenethyl)ammonium tin iodide\",\n        \"formula\": \"(2-ClC6H4C2H4NH3)2SnI4\",\n        \"group\": \"(2-ClPEA)2SnI4, bis(2-chlorophenethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"ClC6H4C2H4NH3\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(2-chlorophenethanaminium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Semiconducting Perovskites (2-XC6H4C2H4NH3)2SnI4 (X = F, Cl, Br): Steric Interaction between the Organic and Inorganic Layers\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"42\",\n        \"pages_start\": \"2031\",\n        \"pages_end\": \"2039\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"SnI2, 2-ClC6H4C2H4NH3I, CH3OH, C6H5CH3\",\n        \"synthesis_product\": \"thin platelike, dark red crystals\",\n        \"synthesis_description\": \"Growing the crystal through the slow evaporation of methanol/toluene mixed solution dissolving the organic and inorganic salts. Adding 52.3 mg (0.140 mmol) SnI2 and 80.0 mg (0.282 mmol) of (2-chlorophenethyl)ammonium iodide into a vial under an inert atmosphere. Then 1.5 mL of anhydrous methanol is added to dissolve the mixture to form a yellow solution. Filtering the solution through a Teflon filter (pore size:\\u2009 0.2 \\u03bcm) and adding 3.0 mL of anhydrous toluene into the solution. The vial is loosely capped and placed for 3 days for the formation of thin platelike, darker red crystals (120 mg, yield 95%) during the slow evaporation process.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Selecting a blocklike crystal under a microscope and attaching it to the end of a quartz fiber with 5 min epoxy. Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo K\\u03b1 radiation), is utilized to collect a full sphere of data at room temperature. A detector distance of approximately 5.0 cm and collection in 2272 frames with increasing \\u03c9 is applied for obtaining intensity data. Using Shelxl 97 to solve and refine the crystal structure.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 1639,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC+vdW\",\n        \"k_point_grid\": \"6x6x1\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"Plane-wave cutoff energy: 500 eV\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"P1\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 1640,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"hydriodic acid (57% w/w in water, Alpha Aesar), phenethylamine (PEA),  lead oxide (PbO, 99%, Sigma-Aldrich)\",\n        \"synthesis_product\": \"Orange (PEA)2PbI4 crystals\",\n        \"synthesis_description\": \"In 30 mL HI solution, PEA, and PbO (ratio: 1.72: 3.45 mmol) were dissolved. The solution was heated at 110\\u00ba C for 4 hours and subsequently cooled to room temperature. Once the solution cooled, single crystals formed.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b12948\",\n        \"dataset_ID\": 1641,\n        \"id\": 414,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead bromide\",\n        \"formula\": \"[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7\",\n        \"group\": \"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, CNH6\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead bromide\",\n        \"last_update\": \"2022-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Hybrid Perovskite-Type Ferroelectric for Highly Polarization-Sensitive Shortwave Photodetection\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"2623\",\n        \"pages_end\": \"2629\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",\n        \"synthesis_product\": \"Yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous  HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",\n        \"experimental_method\": \"Single-Crystal X-ray diffraction\",\n        \"experimental_description\": \"An Agilent Technologies SuperNova Dual Wavelength CCD diffractometer was used, and Mo-K\\u03b1 radiation was performed. CrysAlisPro software was used for data reduction and absorption correction. Shelx software refined structures.\",\n        \"physical_property\": \"200.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc21\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b12948\",\n        \"dataset_ID\": 1642,\n        \"id\": 414,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead bromide\",\n        \"formula\": \"[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7\",\n        \"group\": \"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, CNH6\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead bromide\",\n        \"last_update\": \"2022-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Hybrid Perovskite-Type Ferroelectric for Highly Polarization-Sensitive Shortwave Photodetection\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"2623\",\n        \"pages_end\": \"2629\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",\n        \"synthesis_product\": \"Yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",\n        \"experimental_method\": \"Single-Crystal X-ray diffraction\",\n        \"experimental_description\": \"An Agilent Technologies SuperNova Dual Wavelength CCD diffractometer was used, and Cu-K\\u03b1 radiation was performed. CrysAlisPro software was used for data reduction and absorption correction. Shelx software refined structures.\",\n        \"physical_property\": \"355.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b12948\",\n        \"dataset_ID\": 1643,\n        \"id\": 414,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead bromide\",\n        \"formula\": \"[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7\",\n        \"group\": \"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, CNH6\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead bromide\",\n        \"last_update\": \"2022-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Hybrid Perovskite-Type Ferroelectric for Highly Polarization-Sensitive Shortwave Photodetection\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"2623\",\n        \"pages_end\": \"2629\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",\n        \"synthesis_product\": \"Yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in aqueous  HBr solution (20 mL, 47%). These substances were dissolved through heating and boiling HBr, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved and a clear-yellow solution was resulted. Large crystals grew as the temperature cooled, and the crystals were elongated along crystallographic c-axis.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b12948\",\n        \"dataset_ID\": 1644,\n        \"id\": 414,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead bromide\",\n        \"formula\": \"[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7\",\n        \"group\": \"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, CNH6\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead bromide\",\n        \"last_update\": \"2022-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Hybrid Perovskite-Type Ferroelectric for Highly Polarization-Sensitive Shortwave Photodetection\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"2623\",\n        \"pages_end\": \"2629\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",\n        \"synthesis_product\": \"Yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b12948\",\n        \"dataset_ID\": 1645,\n        \"id\": 414,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead bromide\",\n        \"formula\": \"[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7\",\n        \"group\": \"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, CNH6\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead bromide\",\n        \"last_update\": \"2022-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Hybrid Perovskite-Type Ferroelectric for Highly Polarization-Sensitive Shortwave Photodetection\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"2623\",\n        \"pages_end\": \"2629\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",\n        \"synthesis_product\": \"Yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b12948\",\n        \"dataset_ID\": 1646,\n        \"id\": 414,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead bromide\",\n        \"formula\": \"[CH3(CH2)3NH3]2(CH3NH3)Pb2Br7\",\n        \"group\": \"(BA)2(MA)Pb2Br7, bis(butylaminium) methanaminium septabromo diplumbate(II)\",\n        \"organic\": \"C4H12N, CNH6\",\n        \"inorganic\": \"Pb2Br7, Lead bromide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead bromide\",\n        \"last_update\": \"2022-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"dielectric permittivity\",\n        \"primary_unit\": \"abs. units\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Hybrid Perovskite-Type Ferroelectric for Highly Polarization-Sensitive Shortwave Photodetection\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"2623\",\n        \"pages_end\": \"2629\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbCO3, CH3NH3Br, CH3(CH2)3NH3Br, HBr\",\n        \"synthesis_product\": \"Yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, CH3NH3Br (0.56 g, 0.005 mol) and PbCO3 (2.67 g, 0.01 mol) were dissolved in an aqueous HBr solution (20 mL, 47%) by heating at boiling temperature, producing a bright-yellow solution. Next, CH3(CH2)3NH3Br (1.54 g, 0.01 mol) was added, and a yellow (powder) precipitate formed. By heating this mixture, the solution was redissolved, and a clear-yellow solution resulted. Large crystals grew as the temperature cooled.\",\n        \"experimental_method\": \"AC impedance measurement\",\n        \"experimental_description\": \"Samples were prepared by cutting single crystals along the c-axis, coating crystals with silver conduction paste. The real \\u03ad was measured with two-probe AC impedance method (Impedance Analyzer TH2828A).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.nanolett.7b01544\",\n        \"dataset_ID\": 1647,\n        \"id\": 41,\n        \"compound_name\": \"Formamidinium lead bromide\",\n        \"formula\": \"CH5N2PbBr3\",\n        \"group\": \"Methanimidamide tribromoplumbate(II), FAPBr3, FAPBr, (FA)PbBr3 HC(NH2)2PbBr3, (NH2)2CHPbBr3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Imidoformamidinium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ultrapure Green Light-Emitting Diodes Using Two-Dimensional Formamidinium Perovskites: Achieving Recommendation 2020 Color Coordinates\",\n        \"journal\": \"Nano Letters\",\n        \"vol\": \"9\",\n        \"pages_start\": \"5277\",\n        \"pages_end\": \"5284\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"FABr (0.53M),  PbBr2 (0.4 M), Ethanol, OLA (625 \\u03bcL), OA (25 \\u03bcL),  (Toluene, 12.5 mL\",\n        \"synthesis_product\": \"FAPbBr3\",\n        \"synthesis_description\": \"The 2D perovskite FAPbBr3 was synthesized from a solution that included FABr ( 625 \\u03bcL)dissolved in a non-polar toluene solvent and a polar Ethanol solvent. The nonpolar solvent contained OA and OLA as organic surfactants, which stabilized the solutions. As a result, a precipitate of the solution formed from the poor solubility of perovskites in the nonpolar solvent. This yielded the final product of  FAPbBr3 nanoplatelets in 2.5 mL of Toluene, which was then dissolved in ethanol (375 \\u03bcL) to produce higher and more stable concentrations of FAPbBr3 nanoplatelet.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A CCD spectrometer was used to obtain the absolute absorbance of the colloidal solution in the non-polar solvent of Toluene. The PL of the colloidal solutions were obtained using the Quantaurus QY (C11347-11) from Hamamatsu.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Absorbance\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.nanolett.7b01544\",\n        \"dataset_ID\": 1648,\n        \"id\": 40,\n        \"compound_name\": \"Methylammonium lead bromide\",\n        \"formula\": \"CH3NH3PbBr3\",\n        \"group\": \"Methanaminium tribromoplumbate(II), MAPbBr3, MAPB, (MA)PbBr3, (CH3NH3)PbBr3\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"methanaminium lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ultrapure Green Light-Emitting Diodes Using Two-Dimensional Formamidinium Perovskites: Achieving Recommendation 2020 Color Coordinates\",\n        \"journal\": \"Nano Letters\",\n        \"vol\": \"9\",\n        \"pages_start\": \"5277\",\n        \"pages_end\": \"5284\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"MABr (0.53 M) , PbBr2 (0.4 M), OLA (625 \\u03bcL) and OA (25 \\u03bcL), (Toluene, 12.5 mL)\",\n        \"synthesis_product\": \"MAPbBr3\",\n        \"synthesis_description\": \"The 2D perovskite MAPbBr3 was synthesized from a solution containing MABr (0.53 M) and PbBr2 (0.4M), which was dissolved in a polar DMF solvent. This solution was then mixed with a non-polar Toluene solvent. As a result, a precipitate of MAPbBr3 was formed as nanoplatelets via crystallization.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A CCD spectrometer was used to obtain the absolute absorbance of the colloidal solution in the non-polar solvent of Toluene. The PL of the colloidal solutions were obtained using the Quantaurus QY (C11347-11) from Hamamatsu.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"Absorbance\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1016/j.nanoen.2017.05.005\",\n        \"dataset_ID\": 1649,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Current Density\",\n        \"secondary_unit\": \"mA/cm2\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Thin film perovskite light-emitting diode based on CsPbBr3 powders and interfacial engineering\",\n        \"journal\": \"ScienceDirect\",\n        \"vol\": \"37\",\n        \"pages_start\": \"40\",\n        \"pages_end\": \"45\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"CsBr, PbBr2, DMSO\",\n        \"synthesis_product\": \"CsPbBr3\",\n        \"synthesis_description\": \"The hybrid perovskite CsPbBr3 was prepared from a mixture of CsBr and PbBr2 that was dissolved in a DMSO solvent. The thin films of CsPbBr3 were produced at room temperature via spin-coating and with the addition of chlorobenzene to the mixture.\",\n        \"experimental_method\": \"Luminance of devices\",\n        \"experimental_description\": \"CsPbBr3 thin-film LED samples were displayed to observe the luminance by measuring the wavelength density power emitted by the light source.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9ce00591a\",\n        \"dataset_ID\": 1650,\n        \"id\": 415,\n        \"compound_name\": \"Bis(methylammonium) manganese chloride\",\n        \"formula\": \"(CH3NH3)2MnCl4\",\n        \"group\": \"MA2MnCl4, bis(methanaminium) tetrachloromanganate(II)\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"MnCl4, Manganese chloride\",\n        \"iupac\": \"bis(methanaminium) manganese chloride\",\n        \"last_update\": \"2022-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Centimeter-size square 2D layered Pb-free hybrid perovskite single crystal (CH3NH3)2MnCl4 for red photoluminescence\",\n        \"journal\": \"Royal Society of Chemistry\",\n        \"vol\": \"21\",\n        \"pages_start\": \"4085\",\n        \"pages_end\": \"4091\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"MnCl2 (\\u226599%, A.R. Aladdin), methylammonium chloride (MACl), DMF, DMSO\",\n        \"synthesis_product\": \"MA2MnCl4 single crystals\",\n        \"synthesis_description\": \"The single-crystal hybrid perovskite MA2MnCl4 was synthesized from two solutions. The first solution contained a mixture of MnCl2 and MACl and was dissolved in both DMF and DMSO polar solvents. The solution was then heated to  90 \\u00b0C, which eventually yielded the product. The second method that was used to produce (CH3NH3)2MnCl4 by using a strong acid as the solvent (HCl) was also heated to yield the crystals of the product.\",\n        \"experimental_method\": \"Thermogravimetric (TG) analysis and DSC\",\n        \"experimental_description\": \"TGA was performed by using a STA449C (Netzsch) device.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9ce00591a\",\n        \"dataset_ID\": 1651,\n        \"id\": 415,\n        \"compound_name\": \"Bis(methylammonium) manganese chloride\",\n        \"formula\": \"(CH3NH3)2MnCl4\",\n        \"group\": \"MA2MnCl4, bis(methanaminium) tetrachloromanganate(II)\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"MnCl4, Manganese chloride\",\n        \"iupac\": \"bis(methanaminium) manganese chloride\",\n        \"last_update\": \"2022-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Centimeter-size square 2D layered Pb-free hybrid perovskite single crystal (CH3NH3)2MnCl4 for red photoluminescence\",\n        \"journal\": \"Royal Society of Chemistry\",\n        \"vol\": \"21\",\n        \"pages_start\": \"4085\",\n        \"pages_end\": \"4091\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"MnCl2 (\\u226599%, A.R. Aladdin), methylammonium chloride (MACl), DMF, DMSO\",\n        \"synthesis_product\": \"MA2MnCl4 single crystals\",\n        \"synthesis_description\": \"The single-crystal hybrid perovskite MA2MnCl4 was synthesized from two solutions. The first solution contained a mixture of MnCl2 and MACl and was dissolved in both DMF and DMSO polar solvents. The solution was then heated to 90 \\u00b0C, which eventually yielded the product. The second method that was used to produce (CH3NH3)2MnCl4 by using a strong acid as the solvent (HCl) was also heated to yield the crystals of the product.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"A UV-Vis absorption spectrum was recorded using a UV-2550 spectrometer.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9ce00591a\",\n        \"dataset_ID\": 1652,\n        \"id\": 415,\n        \"compound_name\": \"Bis(methylammonium) manganese chloride\",\n        \"formula\": \"(CH3NH3)2MnCl4\",\n        \"group\": \"MA2MnCl4, bis(methanaminium) tetrachloromanganate(II)\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"MnCl4, Manganese chloride\",\n        \"iupac\": \"bis(methanaminium) manganese chloride\",\n        \"last_update\": \"2022-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Centimeter-size square 2D layered Pb-free hybrid perovskite single crystal (CH3NH3)2MnCl4 for red photoluminescence\",\n        \"journal\": \"Royal Society of Chemistry\",\n        \"vol\": \"21\",\n        \"pages_start\": \"4085\",\n        \"pages_end\": \"4091\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"MnCl2 (\\u226599%, A.R. Aladdin), methylammonium chloride (MACl), DMF, DMSO\",\n        \"synthesis_product\": \"MA2MnCl4 single crystals\",\n        \"synthesis_description\": \"The single-crystal hybrid perovskite MA2MnCl4 was synthesized from two solutions. The first solution contained a mixture of MnCl2 and MACl and was dissolved in both DMF and DMSO polar solvents. The solution was then heated to 90 \\u00b0C, which eventually yielded the product. The second method that was used to produce (CH3NH3)2MnCl4 by using a strong acid as the solvent (HCl) was also heated to yield the crystals of the product.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 of Edinburgh Instruments was used to record the spectra. Lake Shore Cryotronics, Model 336 with ARS-4HW Compressor was used to control the temperature.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"\\u00b0C\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"100 \\u00b0C\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.7b04693\",\n        \"dataset_ID\": 1653,\n        \"id\": 416,\n        \"compound_name\": \"(3-pyrrolinium) cadmium bromide\",\n        \"formula\": \"(C4H8N)CdBr3\",\n        \"group\": \"(3-pyrrolinium)CdBr3, (3-pyrrolinium) tribromocadmate(II)\",\n        \"organic\": \"C4H8N\",\n        \"inorganic\": \"CdBr3, Cadmium bromide\",\n        \"iupac\": \"(3-pyrrolinium) cadmium bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Unprecedented Ferroelectric\\u2013Antiferroelectric\\u2013Paraelectric Phase Transitions Discovered in an Organic\\u2013Inorganic Hybrid Perovskite\",\n        \"journal\": \"American chemical society\",\n        \"vol\": \"139\",\n        \"pages_start\": \"8752\",\n        \"pages_end\": \"8757\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"CdBr2, pyrroline hydrobromide\",\n        \"synthesis_product\": \"Colorless rod-like crystals\",\n        \"synthesis_description\": \"A molar mixture of the precursors was dissolved in water at room temperature. The crystals were grown in the solution by slow evaporation.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Rigaku Saturn 724+ CCD diffractometer with Mo\\u2013K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) were used to collect the diffraction data.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1654,\n        \"id\": 417,\n        \"compound_name\": \"Bis(S-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH2)2SnI4\",\n        \"group\": \"(S-MBA)2SnI4, bis(S-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(S-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-\\u03b1-methylbenzylamine, (S-MBA, 98%, ee 98%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",\n        \"synthesis_product\": \"Orange, rod-like crystals\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), S-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S instrument using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) is utilized to collect a full sphere of diffraction data at 250K and multiscan empirical absorption correction was applied. Within the Olex2 software, using direct methods of the SHELXS program to solve the crystal structure, then utilizing the least-squares method of the SHELXL58 program to refine it.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1655,\n        \"id\": 418,\n        \"compound_name\": \"Bis(R-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH2)2SnI4\",\n        \"group\": \"(R-MBA)2SnI4, bis(R-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(R-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(R)-(+)-\\u03b1-Methylbenzylamine (R-MBA, 98%, ee 96%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",\n        \"synthesis_product\": \"Orange, rod-like crystals\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), R-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S instrument using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) is utilized to collect a full sphere of diffraction data at 250K and multiscan empirical absorption correction was applied. Within the Olex2 software, using direct methods of the SHELXS program to solve the crystal structure, then utilizing the least-squares method of the SHELXL58 program to refine it.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)2(1)2(1)\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1656,\n        \"id\": 419,\n        \"compound_name\": \"Bis(rac-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH2)2SnI4\",\n        \"group\": \"(rac-MBA)2SnI4, bis(rac-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(rac-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(\\u00b1)-\\u03b1-methylbenzylamine (rac-MBA, 99%), Tin(IV) oxide (SnO2, 99.9%), hydriodic acid solution (HI, 57% w/w in water, 99.95%, distilled, stabilized by H3PO2), hypophosphorous acid (H3PO2, 50% w/w in water)\",\n        \"synthesis_product\": \"Orange, rod-like crystals\",\n        \"synthesis_description\": \"SnO2 (0.896 mmol), rac-MBA (1.57 mmol), HI (5.5 mL), and H3PO2 (0.5 mL) were mixed. The solution was heated to 120 degrees Celsius and stirred until it became clear and yellow. Its vial was then put in an oil bath at 90 degrees and then underwent slow cooling at the rate of 1 degree per hour, eventually yielding orange rods. The crystals were filtered in a nitrogen atmosphere and were vacuum dried overnight.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S instrument using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) is utilized to collect a full sphere of diffraction data at 250K and multiscan empirical absorption correction was applied. Within the Olex2 software, using direct methods of the SHELXS program to solve the crystal structure, then utilizing the least-squares method of the SHELXL58 program to refine it.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1657,\n        \"id\": 420,\n        \"compound_name\": \"3-aminopyrrolidinium lead iodide\",\n        \"formula\": \"C4N2H12PbI4\",\n        \"group\": \"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125\\u00baC, held constant until the crystals formed. The temperature was then decreased to 75\\u00ba C, at which most crystals formed. The solution was left to cool to room temperature.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Samples were collected with a Bruker DUO or Molly instrument with Mo K\\u03b1 I\\u03bcS microfocus source (\\u03bb= 0.71073 \\u00c5) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna21\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1658,\n        \"id\": 420,\n        \"compound_name\": \"3-aminopyrrolidinium lead iodide\",\n        \"formula\": \"C4N2H12PbI4\",\n        \"group\": \"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Orange crystal\",\n        \"synthesis_description\": \"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125\\u00baC, held constant until the crystals formed. The temperature was then decreased to 75\\u00ba C, at which most crystals formed. The solution was left to cool to room temperature.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The high-energy absorption edge was extrapolated to imaginary axis. This is parallel to the x-axis (absorption edge is interrupted here by low energy exciton peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna21\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1659,\n        \"id\": 420,\n        \"compound_name\": \"3-aminopyrrolidinium lead iodide\",\n        \"formula\": \"C4N2H12PbI4\",\n        \"group\": \"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"SIESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA in revPBE form + SOC\",\n        \"k_point_grid\": \"3x1x5\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Troullier-Martins pseudpotentials; wave functions: double-\\u03b6 polarized basis set of finite-range numerical pseudoatomic orbitals\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Orange crystal\",\n        \"synthesis_description\": \"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125\\u00baC, held constant, and crystals formed. Temperature continued to decrease to 75\\u00ba C, and most crystals began to form. Sample was left to cool to room temperature.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna21\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1660,\n        \"id\": 421,\n        \"compound_name\": \"3-aminopyrrolidinium lead chloride\",\n        \"formula\": \"C4N2H12PbCl4\",\n        \"group\": \"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"transparent, plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Samples were collected with a Bruker DUO or Molly instrument with Mo K\\u03b1 I\\u03bcS microfocus source (\\u03bb= 0.71073 \\u00c5) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1661,\n        \"id\": 421,\n        \"compound_name\": \"3-aminopyrrolidinium lead chloride\",\n        \"formula\": \"C4N2H12PbCl4\",\n        \"group\": \"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"transparent, plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The high-energy absorption edge was extrapolated to imaginary axis. This is parallel to the x-axis (absorption edge is interrupted here by low energy exciton peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1662,\n        \"id\": 421,\n        \"compound_name\": \"3-aminopyrrolidinium lead chloride\",\n        \"formula\": \"C4N2H12PbCl4\",\n        \"group\": \"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"SIESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA in revPBE form + SOC\",\n        \"k_point_grid\": \"5x1x3\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Pseudopotentials: Troullier-Martins; \\u2022\\tWave-functions: over double-\\u03b6 polarized basis set of finite-range numerical pseudoatomic orbital\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"transparent, plate-shaped crystals g.\",\n        \"synthesis_description\": \"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in a solution of HI (2.5 mL) and H3PO2 (0.5 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Heat was turned off and crystals formed over several days due to the evaporation of the solvent.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1663,\n        \"id\": 422,\n        \"compound_name\": \"3-aminopyrrolidinium lead bromide\",\n        \"formula\": \"C4N2H12PbBr4\",\n        \"group\": \"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Clear, plate-like crystals\",\n        \"synthesis_description\": \"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Samples were collected with a Bruker DUO or Molly instrument with Mo K\\u03b1 I\\u03bcS microfocus source (\\u03bb= 0.71073 \\u00c5) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1664,\n        \"id\": 422,\n        \"compound_name\": \"3-aminopyrrolidinium lead bromide\",\n        \"formula\": \"C4N2H12PbBr4\",\n        \"group\": \"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Clear, plate-like crystals\",\n        \"synthesis_description\": \"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"Single-Crystal X-ray Diffraction\",\n        \"experimental_description\": \"Samples were collected with a Bruker DUO or Molly instrument with Mo K\\u03b1 I\\u03bcS microfocus source (\\u03bb= 0.71073 \\u00c5) with MX Optics. Data were corrected for absorption with APEX3 software, and the Jana 2006 package was used to solve for structures.\",\n        \"physical_property\": \"250.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1665,\n        \"id\": 422,\n        \"compound_name\": \"3-aminopyrrolidinium lead bromide\",\n        \"formula\": \"C4N2H12PbBr4\",\n        \"group\": \"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Clear, plate-like crystals\",\n        \"synthesis_description\": \"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"The high-energy absorption edge was extrapolated to imaginary axis. This is parallel to the x-axis (absorption edge is interrupted here by low energy exciton peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1666,\n        \"id\": 422,\n        \"compound_name\": \"3-aminopyrrolidinium lead bromide\",\n        \"formula\": \"C4N2H12PbBr4\",\n        \"group\": \"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"SIESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA in revPBE form + SOC\",\n        \"k_point_grid\": \"5x1x3\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"Pseudopotentials: Troullier-Martins; Wave-functions: over double-\\u03b6 polarized basis set of finite-range numerical pseudoatomic orbital\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Clear, plate-like crystals\",\n        \"synthesis_description\": \"First, PbO (2 mmol, 446.4 mg) powder was dissolved in a solution of HBr (2.5 mL) and H3PO2 (0.5 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was shut off and plate crystals formed slowly over evaporation of the solvent\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1667,\n        \"id\": 420,\n        \"compound_name\": \"3-aminopyrrolidinium lead iodide\",\n        \"formula\": \"C4N2H12PbI4\",\n        \"group\": \"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Orange crystal\",\n        \"synthesis_description\": \"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125\\u00baC and held constant until the crystals formed. The temperature was then decreased to 75\\u00ba C, at which most crystals formed. The solution was left to cool to room temperature.\",\n        \"experimental_method\": \"UV-vis spectroscopy\",\n        \"experimental_description\": \"Shimadzu UV-2600 UV-vis NIR spectrometer (operating at 200-2500nm region) was used at ambient temperature to collect optical diffuse reflectance measurements. BaSO4 was considered a reference. The band gap of the material was estimated with reflectance v. wavelength data and using the Kubelka-Munk equation \\u03b1/S = (1-R)^{2}(2R)^{-1}.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1668,\n        \"id\": 420,\n        \"compound_name\": \"3-aminopyrrolidinium lead iodide\",\n        \"formula\": \"C4N2H12PbI4\",\n        \"group\": \"(3APr)PbI4, 3-aminopyrrolidinium tetraiodoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Orange crystal\",\n        \"synthesis_description\": \"First, PbO (1 mmol, 223.2 mg) powder was dissolved in a solution of HI (1 mL) and H3PO2 (0.2 mL) while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.25 mmol, 39.75 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. Temperature was reduced to 125\\u00baC and held constant until the crystals formed. The temperature was then decreased to 75\\u00ba C, at which most crystals formed. The solution was left to cool to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Samples were excited with wavelength \\u03bb = 330nm using an optical parametric amplifier.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pna21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1669,\n        \"id\": 422,\n        \"compound_name\": \"3-aminopyrrolidinium lead bromide\",\n        \"formula\": \"C4N2H12PbBr4\",\n        \"group\": \"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Clear, plate-like crystals\",\n        \"synthesis_description\": \"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"UV-vis spectroscopy\",\n        \"experimental_description\": \"Shimadzu UV-2600 UV-vis NIR spectrometer (operating at 200-2500nm region) was used at ambient temperature to collect optical diffuse reflectance measurements. BaSO4 was considered a reference. Band gap of the material was estimated with reflectance v. wavelength data and using the Kubelka-Munk equation \\u03b1/S = (1-R)^{2}(2R)^{-1}.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1670,\n        \"id\": 422,\n        \"compound_name\": \"3-aminopyrrolidinium lead bromide\",\n        \"formula\": \"C4N2H12PbBr4\",\n        \"group\": \"(3APr)PbBr4, 3-aminopyrrolidinium tetrabromoplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HBr, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"Clear, plate-like crystals\",\n        \"synthesis_description\": \"First, PbO (2 mmol, 446.4 mg) powder was dissolved in 2.5 mL of HBr solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (0.4 mmol, 63.6 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Samples were excited with wavelength \\u03bb = 330nm using an optical parametric amplifier.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1671,\n        \"id\": 421,\n        \"compound_name\": \"3-aminopyrrolidinium lead chloride\",\n        \"formula\": \"C4N2H12PbCl4\",\n        \"group\": \"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"transparent, plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"UV-vis spectroscopy\",\n        \"experimental_description\": \"Shimadzu UV-2600 UV-vis NIR spectrometer (operating at 200-2500nm region) was used at ambient temperature to collect optical diffuse reflectance measurements. BaSO4 was considered a reference. Band gap of the material was estimated with reflectance v. wavelength data and using the Kubelka-Munk equation \\u03b1/S = (1-R)^{2}(2R)^{-1}.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b01511\",\n        \"dataset_ID\": 1672,\n        \"id\": 421,\n        \"compound_name\": \"3-aminopyrrolidinium lead chloride\",\n        \"formula\": \"C4N2H12PbCl4\",\n        \"group\": \"(3APr)PbCl4, 3-aminopyrrolidinium tetrachloroplumbate(II)\",\n        \"organic\": \"C4N2H12\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"3-aminopyrrolidinium lead (II) chloride\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Small Cyclic Diammonium Cation Templated (110)-Oriented 2D Halide (X = I, Br, Cl) Perovskites with White-Light Emission\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"3582\",\n        \"pages_end\": \"3590\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, HCl, H3PO2, 3-Amino-pyrrolidine dihydrochloride\",\n        \"synthesis_product\": \"transparent, plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (0.4 mmol, 89.3 mg) powder was dissolved in 2.5 mL of HCl solution and 0.5 mL of H3PO2 while being boiled and stirred. Next, 3-Amino-pyrrolidine dihydrochloride (1.2 mmol, 190.8 mg) was added to the mixture. A precipitate briefly formed but dissolved again under constant stirring and heat. The heat was then turned off, and the crystals formed over several days of slow evaporation.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Samples were excited with wavelength \\u03bb = 330nm using an optical parametric amplifier.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.0c01254.s001\",\n        \"dataset_ID\": 1673,\n        \"id\": 423,\n        \"compound_name\": \"Bis(phenethylammonium) tin bromide\",\n        \"formula\": \"(C6H5CH2CH2NH3)2SnBr4\",\n        \"group\": \"(PEA)2SnBr4, bis(phenethylaminium) tetrabromostannate(II)\",\n        \"organic\": \"C6H5CH2CH2NH3\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"bis(phenethylaminium) tin bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"0D and 2D: The Cases of Phenylethylammonium Tin Bromide Hybrids\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"32\",\n        \"pages_start\": \"4692\",\n        \"pages_end\": \"4698\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnBr2, C6H5CH2CH2NH3Br, HBr, H3PO2\",\n        \"synthesis_product\": \"yellow flake single crystals\",\n        \"synthesis_description\": \"Growing the single crystal through the slow cooling process from 100 \\u00b0C to room temperature. 2.0 mmol of SnBr2 and 4.0 mmol of PEABr are dissolved in a mixture of HBr (3 mL) and H3PO2 (1 mL) after magnetic stirring and nitrogen flow for \\u223c5 min at 100 \\u00b0C. The solution is slowly cooled from 100 \\u00b0C to room temperature. The obtained yellow flake single crystals are washed using acetone and ethyl ether and then dried under reduced pressure.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S diffractometer using a HyPix-6000HE Hybrid Photon Counting (HPC) detector and a dual Mo and Cu microfocus sealed X-ray source as well as a low-temperature Oxford Cryosystem 800 is utilized to collect single-crystal X-ray data.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/cm034267j\",\n        \"dataset_ID\": 1674,\n        \"id\": 424,\n        \"compound_name\": \"2,3,4,5,6-pentafluorophenethylammonium 2-naphthyleneethylammonium tin iodide\",\n        \"formula\": \"C20H21N2F5SnI4\",\n        \"group\": \"(5FPEA\\u00ac\\u2211NEA)SnI4, 2,3,4,5,6-pentafluorophenethylammonium 2-naphthyleneethylammonium tetraiodostannate(II)\",\n        \"organic\": \"C20H21N2F5\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"2,3,4,5,6-pentafluorophenethylammonium 2-naphthyleneethylammonium tin iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"SnI42--Based Hybrid Perovskites Templated by Multiple Organic Cations:\\u2009 Combining Organic Functionalities through Noncovalent Interactions\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"15\",\n        \"pages_start\": \"3632\",\n        \"pages_end\": \"3637\",\n        \"year\": \"2003\",\n        \"synthesis_starting_materials\": \"SnI2, F5C6CH2CH2NH3I, C11H12NI, C2H3N, C7H8O\",\n        \"synthesis_product\": \"platelike, bright red crystals\",\n        \"synthesis_description\": \"Growing the (5FPEA\\u00b7NEA)SnI4 crystals through the slow evaporation of acetonitrile/anisole mixed solution dissolving the organic and inorganic salts. Adding 37.0 mg (0.10 mmol) of SnI2, 34 mg (0.10 mmol) of 2,3,4,5,6-pentafluorophenethylammonium iodide, and 30 mg (0.10 mmol) of 2-naphthyleneethylammonium iodide into a vial under an argon atmosphere. Then 2.0 mL of anhydrous acetonitrile is added to dissolve the mixture to form a yellow solution. Filtering the solution through a Teflon filter (pore size:\\u2009 0.2 \\u03bcm) and adding 2.0 mL of anhydrous anisole into the solution. The vial is loosely capped and placed for 3 days for the formation of platelike, bright red crystals (90 mg, yield 90%).\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Selecting a blocklike crystal under a microscope and attaching it to the end of a quartz fiber with 5 min epoxy. Bruker SMART CCD diffractometer, equipped with a normal focus 2.4 kW sealed tube X-ray source (Mo K\\u03b1 radiation), is utilized to collect a full sphere of data at room temperature. A detector distance of approximately 5.0 cm and collection in 2272 frames with increasing \\u03c9 is applied for obtaining intensity data. Using Shelxl 97 to solve and refine the crystal structure.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03899\",\n        \"dataset_ID\": 1675,\n        \"id\": 417,\n        \"compound_name\": \"Bis(S-)methylbenzylammonium tin iodide\",\n        \"formula\": \"(C6H5CH(CH3)NH2)2SnI4\",\n        \"group\": \"(S-MBA)2SnI4, bis(S-)methylbenzylaminium tetraiodostannate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(S-)methylbenzylaminium tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Distorted Chiral Two-Dimensional Tin Iodide Perovskites for Spin Polarized Charge Transport\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"13030\",\n        \"pages_end\": \"13040\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from a publication\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b05404\",\n        \"dataset_ID\": 1676,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Solution-Phase Synthesis of Cesium Lead Halide Perovskite Nanowires\",\n        \"journal\": \"American Chemistry Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"9230\",\n        \"pages_end\": \"9233\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Cs2CO3 (99.9%, Aldrich), octadecene (ODE, 90%, Aldrich), oleic acid (OA, 90%, Aldrich), PbCl2 (99.999%, Aldrich), PbBr2 (99.999%, Aldrich), PbI2 (99%, Aldrich), oleylamine (OLA, Aldrich, 70%), hexane\",\n        \"synthesis_product\": \"CsPbBr3 and CsPb13\",\n        \"synthesis_description\": \"A solution 5 mL of ODE and 0.18 mmol of PbX2 was degassed under vacuum and were then added to a mixture of OLA and OA, which was annealed at 120 degrees celsius. This solution was kept at a temperature of 150 degrees celsius as 0.6 mL of the inorganic-organic Cs-oleate solution was obtained. The reaction was then placed in a ice-water bath to isolate and purificate CsPbI3 and CsPbBr3 nanowires.\",\n        \"experimental_method\": \"Absorption Spectra\",\n        \"experimental_description\": \"A Shimudzu UV-3010 PC UV-VIS-IR Scanning spectrophotometer equipped with a Shimadzu ISR-3100 was used to obtain the wavelength and absorbance of CsPbBr3.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b05404\",\n        \"dataset_ID\": 1677,\n        \"id\": 38,\n        \"compound_name\": \"Cesium lead iodide\",\n        \"formula\": \"CsPbI3\",\n        \"group\": \"cesium lead iodide, cesium triiodoplumbate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            516,\n            517,\n            518,\n            519,\n            520,\n            521,\n            522\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"nanoform\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Solution-Phase Synthesis of Cesium Lead Halide Perovskite Nanowires\",\n        \"journal\": \"American Chemistry Society\",\n        \"vol\": \"137\",\n        \"pages_start\": \"9230\",\n        \"pages_end\": \"9233\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"Cs2CO3 (99.9%, Aldrich), octadecene (ODE, 90%, Aldrich), oleic acid (OA, 90%, Aldrich), PbCl2 (99.999%, Aldrich), PbBr2 (99.999%, Aldrich), PbI2 (99%, Aldrich), oleylamine (OLA, Aldrich, 70%), hexane\",\n        \"synthesis_product\": \"CsPbI3\",\n        \"synthesis_description\": \"A solution 5 mL of ODE and 0.18 mmol of PbX2 was degassed under vacuum and were then added to a mixture of OLA and OA, which was annealed at 120 degrees celsius. This solution was kept at a temperature of 150 degrees celsius as 0.6 mL of the inorganic-organic Cs-oleate solution was obtained. The reaction was then placed in a ice-water bath to isolate and purificate CsPbI3 and CsPbBr3 nanowires.\",\n        \"experimental_method\": \"Absorption Spectra\",\n        \"experimental_description\": \"A Shimudzu UV-3010 PC UV-VIS-IR Scanning spectrophotometer equipped with a Shimadzu ISR-3100 was used to obtain the wavelength and absorbance of CsPbBr3.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/cm2023696\",\n        \"dataset_ID\": 1678,\n        \"id\": 425,\n        \"compound_name\": \"Bis(phenethylammonium) copper chloride\",\n        \"formula\": \"CuCl4(C6H5CH2CH2NH3)2\",\n        \"group\": \"CuCl4(PEA)2, bis(phenethylaminium) tetrachlorocuprate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CuCl4, Copper chloride\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) copper chloride\",\n        \"last_update\": \"2022-08-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Coexisting Ferromagnetic and Ferroelectric Order in a CuCl4-based Organic\\u2013Inorganic Hybrid\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"24\",\n        \"pages_start\": \"133\",\n        \"pages_end\": \"139\",\n        \"year\": \"2012\",\n        \"synthesis_starting_materials\": \"2-phenyl ethyl ammonium chloride , CuCl2\\u00b72H2O\",\n        \"synthesis_product\": \"square brown plate-like crystals\",\n        \"synthesis_description\": \"Crystals were grown by slowly evaporating an aqueous equimolar solution of the precursors.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using a three-circle Bruker Apex diffractometer equipped with a CCD detector and operating with Mo K\\u03b1 radiation\",\n        \"physical_property\": \"373.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1715,\n        \"id\": 426,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb2I7\",\n        \"formula\": \"C19H31I7N3Pb2I7\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"red crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) was used. Data were collected and corrected for absorption effects with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1716,\n        \"id\": 426,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb2I7\",\n        \"formula\": \"C19H31I7N3Pb2I7\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"red crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1717,\n        \"id\": 426,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb2I7\",\n        \"formula\": \"C19H31I7N3Pb2I7\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"red crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1718,\n        \"id\": 426,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb2I7\",\n        \"formula\": \"C19H31I7N3Pb2I7\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) septaiodo diplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"red crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (78 mg, 0.75 mmol) and methylamine hydrochloride (50 mg, 0.75 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 150 mg (0.58 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference. Wavelength used was \\u03bb = 0.71073 \\u00c5.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1719,\n        \"id\": 427,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb3I10\",\n        \"formula\": \"C20H40I10N4Pb3I10\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"dark brown crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) was used. Data were collected and corrected for absorption effects with APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1720,\n        \"id\": 427,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb3I10\",\n        \"formula\": \"C20H40I10N4Pb3I10\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"dark brown crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1721,\n        \"id\": 427,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb3I10\",\n        \"formula\": \"C20H40I10N4Pb3I10\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"dark brown crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c09647\",\n        \"dataset_ID\": 1722,\n        \"id\": 427,\n        \"compound_name\": \"(PPA)2(MA0.5FA0.5)Pb3I10\",\n        \"formula\": \"C20H40I10N4Pb3I10\",\n        \"group\": \"Bis(3-phenyl-2-propenammonium) decaiodo triplumbate(II)\",\n        \"organic\": \"C9H12N, CNH6, CH5N2\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"(PPA) = 3-phenyl-2-propenammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alternative Organic Spacers for More Efficient Perovskite Solar Cells Containing Ruddlesden\\u2013Popper Phases\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"19705\",\n        \"pages_end\": \"19714\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, formamidinium acetate, methylamine hydrochloride, PPA-I (3-phenyl-2-propenammonium \\u2013 I)\",\n        \"synthesis_product\": \"dark brown crystals\",\n        \"synthesis_description\": \"First, PbO powder (670 mg, 3 mmol) was added to 57% w/w aqueous HI solution (8 mL) in a 20 mL glass vial, and the solution was heated to boiling for ~5 minutes. In this process, the PbO was dissolved. Next, solid formamidinium acetate (104 mg, 1.0 mmol) and methylamine hydrochloride (67 mg, 1 mmol) was added to the solution. This addition resulted in a black powder to precipitate initially, but this was again dissolved under stirring. 60 mg (0.31 mmol) of PPA-I was added slowly, stirring ceased, and the solution cooled to room temperature. Precipitation was complete after ~30 minutes.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Shimadzu UV-3600 PC double-beam, double-monochromator spectrophotometer, operating from 200 to 2500 nm, was used. BaSO4 was used as a non-absorbing reflectance reference. Wavelength of \\u03bb = 0.71073 \\u00c5 was used.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1723,\n        \"id\": 428,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead iodide\",\n        \"formula\": \"(BA)2(MA)Pb2I7\",\n        \"group\": \"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1724,\n        \"id\": 428,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead iodide\",\n        \"formula\": \"(BA)2(MA)Pb2I7\",\n        \"group\": \"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1725,\n        \"id\": 428,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead iodide\",\n        \"formula\": \"(BA)2(MA)Pb2I7\",\n        \"group\": \"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), methylammonium chloride, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"cherry red rectangular-shaped plates\",\n        \"synthesis_description\": \"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 \\u03bcL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1726,\n        \"id\": 428,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead iodide\",\n        \"formula\": \"(BA)2(MA)Pb2I7\",\n        \"group\": \"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), methylammonium chloride, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"cherry red rectangular-shaped plates\",\n        \"synthesis_description\": \"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 \\u03bcL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1727,\n        \"id\": 428,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead iodide\",\n        \"formula\": \"(BA)2(MA)Pb2I7\",\n        \"group\": \"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), methylammonium chloride, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"cherry red rectangular-shaped plates\",\n        \"synthesis_description\": \"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 \\u03bcL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1728,\n        \"id\": 428,\n        \"compound_name\": \"Bis(butylammonium) methylammonium lead iodide\",\n        \"formula\": \"(BA)2(MA)Pb2I7\",\n        \"group\": \"(BA)2(MA)Pb2I7, bis(butylaminium) methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, CNH6\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) methanaminium lead iodide\",\n        \"last_update\": \"2022-01-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, HI, H3PO2, CH3NH3Cl, n-CH3(CH2)3NH2\",\n        \"synthesis_product\": \"cherry red rectangular-shaped plates\",\n        \"synthesis_description\": \"First, PbO powder (2232 mg, 10 mmol) was added to a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol). The solution was heated to boiling and stirred, such that the PbO powder dissolved within 5 minutes. Solid CH3NH3Cl (338 mg, 5 mmol) was added, which caused a black powder to precipitate. The solution was rapidly mixed to redissolve the black powder precipitate. n-CH3(CH2)3NH2 (694 \\u03bcL, 7 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath. This solution was added to the initial solution, causing a black precipitate that soon redissolved under more stirring. The stirring ceased and the solution cooled to room temperature over ~2 hours.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1729,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, FA acetate, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 \\u03bcL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Miniflex600 powder X-ray diffractometer (Cu K\\u03b1 graphite, \\u03bb = 1.5406 \\u00c5) was used. Operating settings included 40 kV/15 mA with K\\u03b2 foil filter.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1730,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, FA acetate, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 \\u03bcL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Miniflex600 powder X-ray diffractometer (Cu K\\u03b1 graphite, \\u03bb = 1.5406 \\u00c5) was used. Operating settings included 40 kV/15 mA with K\\u03b2 foil filter.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1731,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1732,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1733,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1734,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1735,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), FA acetate, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 \\u03bcL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1736,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, FA acetate, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 \\u03bcL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Kubelka-Munk Equation\",\n        \"experimental_description\": \"Reflectance vs. wavelength data was used with the Kubelka-Munk equation to estimate the band gap.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1737,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), FA acetate, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 \\u03bcL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1738,\n        \"id\": 248,\n        \"compound_name\": \"Bis(butylammonium) formamidinium lead iodide\",\n        \"formula\": \"(C4H9NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BA)2[FAPbI3]PbI4, (BA)2(FA)Pb2I7, bis(butane-1-aminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), FA acetate, hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and FA acetate (52.1 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (89.1 \\u03bcL, 0.9 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1739,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, DMA chloride, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Miniflex600 powder X-ray diffractometer (Cu K\\u03b1 graphite, \\u03bb = 1.5406 \\u00c5) was used. Operating settings included 40 kV/15 mA with K\\u03b2 foil filter.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aea2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1740,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, DMA chloride, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Miniflex600 powder X-ray diffractometer (Cu K\\u03b1 graphite, \\u03bb = 1.5406 \\u00c5) was used. Operating settings included 40 kV/15 mA with K\\u03b2 foil filter.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcb\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1741,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcb\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1742,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcb\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1743,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aea2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1744,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aea2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1745,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer (at 200-2500 nm region at 293 K) was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcb\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1746,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer (at 200-2500 nm region at 293 K) was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcb\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1747,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcb\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1748,\n        \"id\": 429,\n        \"compound_name\": \"Bis(butylammonium) dimethylammonium lead iodide\",\n        \"formula\": \"(BA)2(DMA)Pb2I7\",\n        \"group\": \"(BA)2(DMA)Pb2I7, bis(butylaminium) dimethanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C4NH12, C2H8N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) dimethanaminium lead iodide\",\n        \"last_update\": \"2022-01-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), dimethylammonium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and DMA chloride acetate (40.8 mg, 0.5 mmol) were added to 1.75 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6.1 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcb\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1750,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), guanidinium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Miniflex600 powder X-ray diffractometer (Cu K\\u03b1 graphite, \\u03bb = 1.5406 \\u00c5) was used. Operating settings included 40 kV/15 mA with K\\u03b2 foil filter.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1751,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, GA chloride, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Miniflex600 powder X-ray diffractometer (Cu K\\u03b1 graphite, \\u03bb = 1.5406 \\u00c5) was used. Operating settings included 40 kV/15 mA with K\\u03b2 foil filter.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1752,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1753,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1754,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1755,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VASP\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"HSE+SOC\",\n        \"k_point_grid\": \"4x2x2 k-grid (primitive cells) and 4x1x1 for inorganic 2D model compounds\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1756,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), guanidinium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer was used. BaSO4 was used as a reference of 100% reflectance for all measurements.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1757,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, GA chloride, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Kubelka-Munk Equation\",\n        \"experimental_description\": \"Reflectance vs. wavelength data was used with the Kubelka-Munk equation to estimate the band gap.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1758,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO (99.9%), guanidinium chloride (99%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), butylamine, hypophosphorous acid solution (H3PO2, 50 wt % in H2O)\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"Photoluminescence microscopy\",\n        \"experimental_description\": \"A Horiba LabRAM HR Evolution confocal Raman microscope was used with a 473 nm laser to excite samples at 50x magnification.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03860\",\n        \"dataset_ID\": 1759,\n        \"id\": 430,\n        \"compound_name\": \"Bis(butylammonium) guanidinium lead iodide\",\n        \"formula\": \"(BA)2(GA)Pb2I7\",\n        \"group\": \"(BA)2(GA)Pb2I7, bis(butylaminium) diaminomethanaminium septaiodoplumbate(II)\",\n        \"organic\": \"C4NH12, CN3H8\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(butylaminium) diaminomethanaminium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Negative Pressure Engineering with Large Cage Cations in 2D Halide Perovskites Causes Lattice Softening\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"11486\",\n        \"pages_end\": \"11496\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO, GA chloride, HI, BA, H3PO2\",\n        \"synthesis_product\": \"red plate-shaped crystals\",\n        \"synthesis_description\": \"First, PbO (223 mg, 1 mmol) and GA chloride (47.8 mg, 0.5 mmol) were added to 1.5 mL of concentrated HI solution. These substances were dissolved under constant stirring and heating. Then, BA (49.6 \\u03bcL, 0.5 mmol) was added to 0.25 mL of concentrated aqueous H3PO2 in a separate vial. This solution was stirred and was soon added to the initial solution. The temperature was lowered to 125\\u00ba C until crystals began to form. The temperature was lowered again to 80\\u00baC, the hot plate was turned off after 60 minutes, and after 30 minutes thereafter, the crystals were collected.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmcm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1760,\n        \"id\": 431,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead bromide\",\n        \"formula\": \"C6H10N2Pb2Br6\",\n        \"group\": \"(dmpz)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dimethylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, pyrazine, MeOH\",\n        \"synthesis_product\": \"dark red plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80\\u00baC. After 24 hours, crystals began to precipitate.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. Wavelength used was \\u03bb = 0.7749 \\u00c5.\",\n        \"physical_property\": \"298.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1761,\n        \"id\": 431,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead bromide\",\n        \"formula\": \"C6H10N2Pb2Br6\",\n        \"group\": \"(dmpz)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dimethylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, pyrazine, MeOH\",\n        \"synthesis_product\": \"dark red plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80\\u00baC. After 24 hours, crystals began to precipitate.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (\\u03b1/S)^{2}, where \\u03b1 = absorption coefficient and S = scattering coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1762,\n        \"id\": 431,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead bromide\",\n        \"formula\": \"C6H10N2Pb2Br6\",\n        \"group\": \"(dmpz)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dimethylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Electron Paramagnetic Resonance (EPR) Spectra\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Magnetic Field\",\n        \"secondary_unit\": \"G\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, pyrazine, MeOH\",\n        \"synthesis_product\": \"dark red plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80\\u00baC. After 24 hours, crystals began to precipitate.\",\n        \"experimental_method\": \"EPR\",\n        \"experimental_description\": \"A Bruker EMX spectrometer, an ER 041 XG microwave bridge, and an ER4116DM cavity were used at 77 K, frequency ~9.6 GHz, and a sweep time of 30 seconds.\",\n        \"physical_property\": \"77.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1763,\n        \"id\": 431,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead bromide\",\n        \"formula\": \"C6H10N2Pb2Br6\",\n        \"group\": \"(dmpz)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dimethylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, pyrazine, MeOH\",\n        \"synthesis_product\": \"dark red plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 1 mL); meanwhile, solid pyrazine (20 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 1 mL). The solutions were combined, MeOH (0.2 mL) was added, and the vial was capped and heated at 80\\u00baC. After 24 hours, crystals began to precipitate.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1764,\n        \"id\": 432,\n        \"compound_name\": \"N-Hydro-N\\u2032-methylpyrazinium lead bromide iodide\",\n        \"formula\": \"C5H8N2Pb2Br4.5I1.5\",\n        \"group\": \"(Hmpz)[Pb2Br4.5I1.5], bis(N-hydro-N\\u201a\\u00c4\\u2264-methylpyrazinium) nonabromo triiodo tetraplumbate(II)\",\n        \"organic\": \"C5H8N2\",\n        \"inorganic\": \"Pb2Br4.5I1.5, Lead bromide iodide\",\n        \"iupac\": \"N-hydro-N\\u2032-methylpyrazinium lead bromide iodide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hmpz = N-Hydro-N\\u2019-methylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (mpz)I\",\n        \"synthesis_product\": \"dark red crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (mpz)I (55 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the solution was remained undisturbed at room temperature, until crystals were obtained at 2 hours.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. \\u03bb = 0.7749 \\u00c5.\",\n        \"physical_property\": \"298.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1765,\n        \"id\": 432,\n        \"compound_name\": \"N-Hydro-N\\u2032-methylpyrazinium lead bromide iodide\",\n        \"formula\": \"C5H8N2Pb2Br4.5I1.5\",\n        \"group\": \"(Hmpz)[Pb2Br4.5I1.5], bis(N-hydro-N\\u201a\\u00c4\\u2264-methylpyrazinium) nonabromo triiodo tetraplumbate(II)\",\n        \"organic\": \"C5H8N2\",\n        \"inorganic\": \"Pb2Br4.5I1.5, Lead bromide iodide\",\n        \"iupac\": \"N-hydro-N\\u2032-methylpyrazinium lead bromide iodide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hmpz = N-Hydro-N\\u2019-methylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (mpz)I\",\n        \"synthesis_product\": \"dark red crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (mpz)I (55 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the solution was remained undisturbed at room temperature, until crystals were obtained at 2 hours.\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (\\u03b1/S)^{2}, where \\u03b1 = absorption coefficient and S = scattering coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1766,\n        \"id\": 432,\n        \"compound_name\": \"N-Hydro-N\\u2032-methylpyrazinium lead bromide iodide\",\n        \"formula\": \"C5H8N2Pb2Br4.5I1.5\",\n        \"group\": \"(Hmpz)[Pb2Br4.5I1.5], bis(N-hydro-N\\u201a\\u00c4\\u2264-methylpyrazinium) nonabromo triiodo tetraplumbate(II)\",\n        \"organic\": \"C5H8N2\",\n        \"inorganic\": \"Pb2Br4.5I1.5, Lead bromide iodide\",\n        \"iupac\": \"N-hydro-N\\u2032-methylpyrazinium lead bromide iodide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hmpz = N-Hydro-N\\u2019-methylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (mpz)I\",\n        \"synthesis_product\": \"dark red crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (mpz)I (55 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the solution was remained undisturbed at room temperature, until crystals were obtained at 2 hours.\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1767,\n        \"id\": 433,\n        \"compound_name\": \"N-Hydro-N\\u2032-ethylpyrazinium lead bromide\",\n        \"formula\": \"C6H10N2Pb2Br6\",\n        \"group\": \"(Hepz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-ethylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-ethylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hepz = N-Hydro-N\\u2019-ethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (epz)I\",\n        \"synthesis_product\": \"dark red crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (epz)I (59 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, remained undisturbed at room temperature, and crystals were obtained within 2 hours.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. \\u03bb = 0.7749 \\u00c5.\",\n        \"physical_property\": \"298.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmmm\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1768,\n        \"id\": 433,\n        \"compound_name\": \"N-Hydro-N\\u2032-ethylpyrazinium lead bromide\",\n        \"formula\": \"C6H10N2Pb2Br6\",\n        \"group\": \"(Hepz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-ethylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-ethylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hepz = N-Hydro-N\\u2019-ethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (epz)I\",\n        \"synthesis_product\": \"dark red crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (epz)I (59 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, remained undisturbed at room temperature, and crystals were obtained within 2 hours.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (\\u03b1/S)^{2}, where \\u03b1 = absorption coefficient and S = scattering coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmmm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1769,\n        \"id\": 433,\n        \"compound_name\": \"N-Hydro-N\\u2032-ethylpyrazinium lead bromide\",\n        \"formula\": \"C6H10N2Pb2Br6\",\n        \"group\": \"(Hepz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-ethylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-ethylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hepz = N-Hydro-N\\u2019-ethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (epz)I\",\n        \"synthesis_product\": \"dark red crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (epz)I (59 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, remained undisturbed at room temperature, and crystals were obtained within 2 hours.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmmm\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1770,\n        \"id\": 434,\n        \"compound_name\": \"N-Hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"formula\": \"C7H12N2Pb2Br6\",\n        \"group\": \"(Hppz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-isopropylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C7H12N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hppz = N-Hydro-N\\u2019-isopropylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (ppz)I\",\n        \"synthesis_product\": \"dark red rhombic-plate crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. \\u03bb = 0.6888 \\u00c5.\",\n        \"physical_property\": \"298.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Amm2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1771,\n        \"id\": 434,\n        \"compound_name\": \"N-Hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"formula\": \"C7H12N2Pb2Br6\",\n        \"group\": \"(Hppz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-isopropylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C7H12N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hppz = N-Hydro-N\\u2019-isopropylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (ppz)I\",\n        \"synthesis_product\": \"dark red rhombic-plate crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (\\u03b1/S)^{2}, where \\u03b1 = absorption coefficient and S = scattering coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Amm2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1772,\n        \"id\": 434,\n        \"compound_name\": \"N-Hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"formula\": \"C7H12N2Pb2Br6\",\n        \"group\": \"(Hppz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-isopropylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C7H12N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hppz = N-Hydro-N\\u2019-isopropylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (ppz)I\",\n        \"synthesis_product\": \"dark red rhombic-plate crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"25.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Amm2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1773,\n        \"id\": 434,\n        \"compound_name\": \"N-Hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"formula\": \"C7H12N2Pb2Br6\",\n        \"group\": \"(Hppz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-isopropylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C7H12N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hppz = N-Hydro-N\\u2019-isopropylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (ppz)I\",\n        \"synthesis_product\": \"dark red rhombic-plate crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"A Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector was used for emission and excitation spectra. FluorEssence 2.3.15 software was used to collect data.\",\n        \"physical_property\": \"80.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Amm2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1774,\n        \"id\": 434,\n        \"compound_name\": \"N-Hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"formula\": \"C7H12N2Pb2Br6\",\n        \"group\": \"(Hppz)[Pb2Br6], N-hydro-N\\u201a\\u00c4\\u2264-isopropylpyrazinium hexabromo diplumbate(II)\",\n        \"organic\": \"C7H12N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N-hydro-N\\u2032-isopropylpyrazinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"Hppz = N-Hydro-N\\u2019-isopropylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, HBr, (ppz)I\",\n        \"synthesis_product\": \"dark red rhombic-plate crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (184 mg, 0.501 mmol) was dissolved in HBr aq. (9 M, 0.25 mL); meanwhile, solid (ppz)I (63 mg, 0.25 mmol) was dissolved in HBr aq. (9 M, 0.25 mL). The solutions were combined, and the final mixture remained undisturbed at room temperature. Crystals formed within 12 hours.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Amm2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1775,\n        \"id\": 435,\n        \"compound_name\": \"N,N\\u2032-Dihydro-3-amidinopyridinium lead bromide\",\n        \"formula\": \"C6H9N3Pb2Br6\",\n        \"group\": \"(H2apy)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dihydro-3-amidinopyridinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H9N3\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dihydro-3-amidinopyridinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"H2apy = N,N\\u2019-Dihydro-3-amidinopyridinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, 3-amidinopyridine hydrobromide, HBr\",\n        \"synthesis_product\": \"pale yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (196 mg, 0.534 mmol) and 3-amidinopyridine hydrobromide (40.5 mg, 0.200 mmol) were combined. HBr aq. (9 M, 2.0 mL) was added to the mixture, and a yellow solution formed. The solution was heated to 100\\u00baC for 4 hours. Then, the solution cooled at a constant rate of 5\\u00baC per hour, obtaining the crystals.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. \\u03bb = 0.7288 \\u00c5.\",\n        \"physical_property\": \"298.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Iba2\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1776,\n        \"id\": 435,\n        \"compound_name\": \"N,N\\u2032-Dihydro-3-amidinopyridinium lead bromide\",\n        \"formula\": \"C6H9N3Pb2Br6\",\n        \"group\": \"(H2apy)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dihydro-3-amidinopyridinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H9N3\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dihydro-3-amidinopyridinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"H2apy = N,N\\u2019-Dihydro-3-amidinopyridinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, 3-amidinopyridine hydrobromide, HBr\",\n        \"synthesis_product\": \"pale yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (196 mg, 0.534 mmol) and 3-amidinopyridine hydrobromide (40.5 mg, 0.200 mmol) were combined. HBr aq. (9 M, 2.0 mL) was added to the mixture, and a yellow solution formed. The solution was heated to 100\\u00baC for 4 hours. Then, the solution cooled at a constant rate of 5\\u00baC per hour, obtaining the crystals.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector was used for emission and excitation spectra. FluorEssence 2.3.15 software was used to collect data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Iba2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1777,\n        \"id\": 435,\n        \"compound_name\": \"N,N\\u2032-Dihydro-3-amidinopyridinium lead bromide\",\n        \"formula\": \"C6H9N3Pb2Br6\",\n        \"group\": \"(H2apy)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dihydro-3-amidinopyridinium hexabromo diplumbate(II)\",\n        \"organic\": \"C6H9N3\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dihydro-3-amidinopyridinium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"H2apy = N,N\\u2019-Dihydro-3-amidinopyridinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, 3-amidinopyridine hydrobromide, HBr\",\n        \"synthesis_product\": \"pale yellow plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (196 mg, 0.534 mmol) and 3-amidinopyridine hydrobromide (40.5 mg, 0.200 mmol) were combined. HBr aq. (9 M, 2.0 mL) was added to the mixture, and a yellow solution formed. The solution was heated to 100\\u00baC for 4 hours. Then, the solution cooled at a constant rate of 5\\u00baC per hour, obtaining the crystals.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Iba2\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1778,\n        \"id\": 436,\n        \"compound_name\": \"N,N\\u2032-Dihydro-1,3-propanediammonium lead bromide\",\n        \"formula\": \"C3H12N2Pb2Br6\",\n        \"group\": \"(H2dap)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dihydro-1,3-propanediammonium hexabromo diplumbate(II)\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dihydro-1,3-propanediammonium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"H2dap = N,N\\u2019-Dihydro-1,3-propanediammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. \\u03bb = 0.71073 \\u00c5.\",\n        \"physical_property\": \"296.2\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1779,\n        \"id\": 436,\n        \"compound_name\": \"N,N\\u2032-Dihydro-1,3-propanediammonium lead bromide\",\n        \"formula\": \"C3H12N2Pb2Br6\",\n        \"group\": \"(H2dap)[Pb2Br6], N,N\\u201a\\u00c4\\u2264-dihydro-1,3-propanediammonium hexabromo diplumbate(II)\",\n        \"organic\": \"C3H12N2\",\n        \"inorganic\": \"Pb2Br6, Lead bromide\",\n        \"iupac\": \"N,N\\u2032-dihydro-1,3-propanediammonium lead bromide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"H2dap = N,N\\u2019-Dihydro-1,3-propanediammonium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbBr2, 1,2-dap, HBr\",\n        \"synthesis_product\": \"colorless needle-like crystals\",\n        \"synthesis_description\": \"First, solid PbBr2 (171 mg, 0.465 mmol) and liquid 1,2-dap (13.2 \\u03bcL, 0.157 mmol) were added, in a 3:1 ratio, in HBr aq. Solution (4.45 M, 0.7 mL). The solution was heated to 100\\u00baC and stirred. The solution then cooled to room temperature at a rate of 3\\u00baC per hour, the precipitate was dried under reduced pressure for 12 hours, and crystals were obtained.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The excitation spectra was collected with a Horiba Jobin-Yvon Nanolog fluorimeter with a 450-W xenon lamp and R928P detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1780,\n        \"id\": 437,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead iodide\",\n        \"formula\": \"C6H10N2Pb2I6\",\n        \"group\": \"(dmpz)[Pb2I6],N, N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"N, N\\u2032-dimethylpyrazinium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption coefficient\",\n        \"primary_unit\": \"mm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, NaI, GBL, dmpz(BF4)2\",\n        \"synthesis_product\": \"opaque black plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. \\u03bb = 0.7288 \\u00c5.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1781,\n        \"id\": 437,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead iodide\",\n        \"formula\": \"C6H10N2Pb2I6\",\n        \"group\": \"(dmpz)[Pb2I6],N, N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"N, N\\u2032-dimethylpyrazinium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, NaI, GBL, dmpz(BF4)2\",\n        \"synthesis_product\": \"opaque black plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1782,\n        \"id\": 437,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead iodide\",\n        \"formula\": \"C6H10N2Pb2I6\",\n        \"group\": \"(dmpz)[Pb2I6],N, N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"N, N\\u2032-dimethylpyrazinium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, NaI, GBL, dmpz(BF4)2\",\n        \"synthesis_product\": \"opaque black plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1783,\n        \"id\": 437,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead iodide\",\n        \"formula\": \"C6H10N2Pb2I6\",\n        \"group\": \"(dmpz)[Pb2I6],N, N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"N, N\\u2032-dimethylpyrazinium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, NaI, GBL, dmpz(BF4)2\",\n        \"synthesis_product\": \"opaque black plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",\n        \"experimental_method\": \"UV-vis absorbance\",\n        \"experimental_description\": \"A Shimadzu UV-2600 spectrometer was used to collect the diffuse reflectance measurements, and the Kubelka-Munk function was used to transform the data. Absorption measurements were collected with a spin-coated film, using an Agilent Cary 6000i spectrometer. The band gap was found by normalizing (\\u03b1/S)^{2}, where \\u03b1 = absorption coefficient and S = scattering coefficient.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1784,\n        \"id\": 437,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead iodide\",\n        \"formula\": \"C6H10N2Pb2I6\",\n        \"group\": \"(dmpz)[Pb2I6],N, N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"N, N\\u2032-dimethylpyrazinium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Conductivity\",\n        \"primary_unit\": \"S\\u2022cm^{-1}\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"pellet\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, NaI, GBL, dmpz(BF4)2\",\n        \"synthesis_product\": \"opaque black plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",\n        \"experimental_method\": \"Conductivity\",\n        \"experimental_description\": \"Powder was dehydrated under reduced pressure and pressed into circular pellets. Conductivity was measured on the pellets by using a Bio-Logic VSP300 Potentiostat/Galvanostat. Cyclic voltagramms vs. open circuit potential were found, a best fit line was generated to find resistance, and conductivity was found by \\u03c3=1/\\u03c1, where \\u03c1 = (wtR)/L.\",\n        \"physical_property\": \"378.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1785,\n        \"id\": 437,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead iodide\",\n        \"formula\": \"C6H10N2Pb2I6\",\n        \"group\": \"(dmpz)[Pb2I6],N, N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"N, N\\u2032-dimethylpyrazinium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"activation energy for electrical conduction\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"pellet\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, NaI, GBL, dmpz(BF4)2\",\n        \"synthesis_product\": \"opaque black plate-shaped crystals\",\n        \"synthesis_description\": \": First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",\n        \"experimental_method\": \"Conductivity\",\n        \"experimental_description\": \"Powder was dehydrated under reduced pressure and pressed into circular pellets. Conductivity was measured on the pellets by using a Bio-Logic VSP300 Potentiostat/Galvanostat. Cyclic voltagramms vs. open circuit potential were found, a best fit line was generated to find resistance, and conductivity was found by \\u03c3=1/\\u03c1, where \\u03c1 = (wtR)/L.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202005012\",\n        \"dataset_ID\": 1786,\n        \"id\": 437,\n        \"compound_name\": \"N, N\\u2032-Dimethylpyrazinium lead iodide\",\n        \"formula\": \"C6H10N2Pb2I6\",\n        \"group\": \"(dmpz)[Pb2I6],N, N\\u201a\\u00c4\\u2264-dimethylpyrazinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"N, N\\u2032-dimethylpyrazinium lead iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"dmpz = N, N\\u2019-Dimethylpyrazinium\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Conductivity\",\n        \"primary_unit\": \"S\\u2022cm^{-1}\",\n        \"secondary_name\": \"1/T\",\n        \"secondary_unit\": \"K^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Expanded Analogs of Three\\u2010Dimensional Lead\\u2010Halide Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"19087\",\n        \"pages_end\": \"19094\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, NaI, GBL, dmpz(BF4)2\",\n        \"synthesis_product\": \"opaque black plate-shaped crystals\",\n        \"synthesis_description\": \"First, solid PbI2 (46 mg, 0.1 mmol) and NaI (15 mg, 0.1 mmol) were dissolved in 5 mL of GBL, and 1 mL of this solution was poured into a 5-mm diameter glass tibe with 0.3 mL of GBL layered on top. Solid dmpz(BF4)2 (3 mg, 0.01 mmol) was dissolved in GBL (1 mL), and this was added on top of the GBL layer. After 24 hours, crystals were obtained.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"Powder was dehydrated under reduced pressure and pressed into circular pellets. Conductivity was measured on the pellets by using a Bio-Logic VSP300 Potentiostat/Galvanostat. Cyclic voltagramms vs. open circuit potential were found, a best fit line was generated to find resistance, and conductivity was found by \\u03c3=1/\\u03c1, where \\u03c1 = (wtR)/L.\",\n        \"physical_property\": \"378.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbam\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.joc.9b02769\",\n        \"dataset_ID\": 1787,\n        \"id\": 438,\n        \"compound_name\": \"thieno[3,2-b]thiophene\",\n        \"formula\": \"C6H4S2\",\n        \"group\": \"TbT\",\n        \"organic\": \"C6H4\",\n        \"inorganic\": \"S2\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tetrasubstituted Thieno[3,2-b]thiophenes as Hole-Transporting Materials for Perovskite Solar Cells\",\n        \"journal\": \"ACS\",\n        \"vol\": \"https://doi.org/10.1021/acs.joc.9b02769\",\n        \"pages_start\": \"224\",\n        \"pages_end\": \"233\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Ether (700 mL), 3-(2,2-diethoxy-ethylsulfanyl)thiophene, 1.5 M tert-butyllithium e (400 mL, 0.600 mol)\",\n        \"synthesis_product\": \"Thieno[3,2-b]thiophene\",\n        \"synthesis_description\": \"3-(2,2-diethoxy-ethylsulfanyl)thiophene (32.8 g, 154 mmol) was stirred with a solution of ether (700 mL) and was heated for 10 h. The mixture was then filtered via a Buchner Funnel filter. The solvent was then removed and the residue was purified by column chromatography on silica gel. This process produced Thieno[3,2-b]thiophene.\",\n        \"experimental_method\": \"Absorbance spectra\",\n        \"experimental_description\": \"UV-Visible spectrophotometer in CH2Cl2 solution was collected on a Nicolet AVATAR 360 FT-IR instrument.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/ol9010745\",\n        \"dataset_ID\": 1788,\n        \"id\": 438,\n        \"compound_name\": \"thieno[3,2-b]thiophene\",\n        \"formula\": \"C6H4S2\",\n        \"group\": \"TbT\",\n        \"organic\": \"C6H4\",\n        \"inorganic\": \"S2\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Facile and Scalable Synthesis of the Fused-Ring Heterocycles Thieno[3,2-b]thiophene and Thieno[3,2-b]furan\",\n        \"journal\": \"ACS\",\n        \"vol\": \"14\",\n        \"pages_start\": \"3144\",\n        \"pages_end\": \"3147\",\n        \"year\": \"2009\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1039/C7EE03113K\",\n        \"dataset_ID\": 1790,\n        \"id\": 440,\n        \"compound_name\": \"Acetylacetonate methylammonium iodide gallium\",\n        \"formula\": \"C16H28GaINO6\",\n        \"group\": \"GaAA3-MAI\",\n        \"organic\": \"C16H28\",\n        \"inorganic\": \"GaINO6\",\n        \"iupac\": \"4-oxopent-2-en-2-olate methanaminium gallium iodide\",\n        \"last_update\": \"2022-08-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"In situ induced core/shell stabilized hybrid perovskites via gallium(iii) acetylacetonate intermediate towards highly efficient and stable solar cells\",\n        \"journal\": \"Royal Society of Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"286\",\n        \"pages_end\": \"293\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using Gemini S Ultra CCD area-detector diffractometer.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual Extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1039/C7EE03113K\",\n        \"dataset_ID\": 1791,\n        \"id\": 441,\n        \"compound_name\": \"Acetylacetonate gallium\",\n        \"formula\": \"C15H21GaO6\",\n        \"group\": \"GaAA3\",\n        \"organic\": \"C15H21\",\n        \"inorganic\": \"GaO6\",\n        \"iupac\": \"4-oxopent-2-en-2-olate gallium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"In situ induced core/shell stabilized hybrid perovskites via gallium(iii) acetylacetonate intermediate towards highly efficient and stable solar cells\",\n        \"journal\": \"Royal Society of Chemistry\",\n        \"vol\": \"11\",\n        \"pages_start\": \"286\",\n        \"pages_end\": \"293\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"acetylacetonate solvent\",\n        \"synthesis_product\": \"GaAA3\",\n        \"synthesis_description\": \"GaAA3 was synthesized by 100 mg GaAA3 in 1ml acetylacetonate solvent. The solution was placed at  100 degrees celsius and stirred until single crystals of the product was produced.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"14\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acsenergylett.6b00327\",\n        \"dataset_ID\": 1792,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect Passivation of Organic-Inorganic Hybrid Perovskites by Diammonium Iodide towards High-Performance Photovoltaic Devices\",\n        \"journal\": \"ACS\",\n        \"vol\": \"4\",\n        \"pages_start\": \"757\",\n        \"pages_end\": \"763\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41427-019-0131-0\",\n        \"dataset_ID\": 1793,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Mixed-halide perovskite synthesis by chemical reaction and crystal nucleation under an optical potential\",\n        \"journal\": \"NPG Asia Materials\",\n        \"vol\": \"11\",\n        \"pages_start\": \"31\",\n        \"pages_end\": \"31\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"MACl (TCI, >98.0%), PbCl2 (Aldrich, 98.0%), dimethyl sulfoxide (DMSO) (Wako), and N, N-dimethylformamide (DMF) (Wako)\",\n        \"synthesis_product\": \"Single crystalline colorless MAPbCl3 with the size of several hundred micrometers\",\n        \"synthesis_description\": \"Optical trapping induced crystallization:\\r\\n1:1 MACl/PbCl2 (1.0 M) were dissolved in DMSO: DMF solvent mixture (1:1, v-v) to prepare the precursor solution. The solution was centrifuged at 10,000\\u2009r.p.m for 5\\u2009min; the supernatant was used for further experiments. \\r\\n10\\u2009\\u03bcL of the supernatant solution was used to prepare a thin layer (100-200 um thickness) in a laboratory-built sample chamber. A near-infrared (NIR) laser (Spectron Laser System, \\u03bb\\u2009=\\u20091064\\u2009nm) was focused onto the solution surface through an objective lens at 60 times magnification (Olympus UPlanFLN with a numerical aperture of 0.90).\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"The crystal was mounted on the glass capillary and fixed with epoxy resin. Crystallographic data were collected using a Rigaku RAXIS-RAPID diffractometer with Mo-K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation from a graphite monochromator. Structural refinements were performed using the full-matrix least-squares method on F2. The calculations were carried out with the Yadokari-XG software.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Pm(-3)m\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1794,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic  acid (HI, 57  wt.  %  in  H2O, distilled, stabilized,   99.95%), hypophosphorous  acid  solution (H3PO2, 50  wt.  %  in  H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) was used to perform the XRD. Data was collected, integrated, and corrected for absorption with the APEX3 software.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1795,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) was used to perform the XRD. Data was collected, integrated, and corrected for absorption with the APEX3 software.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1796,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb = 0.71073 \\u00c5) was used to perform the XRD. Data was collected, integrated, and corrected for absorption with the APEX3 software.\",\n        \"physical_property\": \"440.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Ibam\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1797,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere. The PLQE was found by computing the ration of emitted photons to absorbed photons.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1798,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",\n        \"synthesis_product\": \"colorless 60 nm thick film\",\n        \"synthesis_description\": \"0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere. The PLQE was found by computing the ration of emitted photons to absorbed photons.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1799,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam/double monochromator spectrophotometer was used to collect the data. The device was operated between 200 and 2500 nm. The non-absorbing reflectance reference was BaSO4. To find the estimated band gap of the material, the reflectance was converted to absorbance via the Kubelka-Munk equation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1800,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",\n        \"synthesis_product\": \"colorless 60 nm thick film\",\n        \"synthesis_description\": \"0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam/double monochromator spectrophotometer was used to collect the data. The device was operated between 200 and 2500 nm. The non-absorbing reflectance reference was BaSO4. To find the estimated band gap of the material, the reflectance was converted to absorbance via the Kubelka-Munk equation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1801,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"TGA measurement\",\n        \"experimental_description\": \"A Netzsch Simultaneous Thermal Analysis (STA) system was used with around 15 mg of the sample. The sample was heated to 750\\u00baC with a heating rate of 8\\u00baC/min.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1802,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"PL measurement\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1803,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",\n        \"synthesis_product\": \"colorless 60 nm thick film\",\n        \"synthesis_description\": \"0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.\",\n        \"experimental_method\": \"PL measurement\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1804,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\",\n        \"physical_property\": \"295.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1805,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\",\n        \"physical_property\": \"145.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1806,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\",\n        \"physical_property\": \"115.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1807,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1808,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), octylenediammonium diodide (DAO-I2), DMF\",\n        \"synthesis_product\": \"colorless 60 nm thick film\",\n        \"synthesis_description\": \"0.25 M solution of the precursor salts (1:1 molar ratio) in DMF was prepared by heating at 70 degrees C for 15 minutes. The solution was spin-coated on substrate at 4000 rpm for 30 s and annealed at 100 degrees C for 10 min in a glove box.\",\n        \"experimental_method\": \"PL measurement\",\n        \"experimental_description\": \"A Horiba LabRam Evolution high-resolution confocal Raman microscope spectrometer (600 g/mm diffraction grating) was used, along with a laser of 473 nm at a 0.1%-0.01% of max power output. The temperature-dependent PL measurements were performed by using a 405-nm diode laser to excite the samples, and QE was found by using a Horiba Jobin-Yvon Nanolog spectrofluorometer and an integrating sphere.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c03004\",\n        \"dataset_ID\": 1809,\n        \"id\": 444,\n        \"compound_name\": \"1,8-octyldiammonium tin iodide\",\n        \"formula\": \"(DAO)Sn2I6\",\n        \"group\": \"(DAO)Sn2I6, 1,8-octyldiaminium hexaiodo distannate(II)\",\n        \"organic\": \"C8N2H24\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"1,8-octyldiaminium tin iodide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Water-Stable 1D Hybrid Tin(II) Iodide Emits Broad Light with 36% Photoluminescence Quantum Efficiency\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"9028\",\n        \"pages_end\": \"9038\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) chloride dihydrate (SnCl2 x 2H2O), hydriodic acid (HI, 57 wt. % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt. % in H2O), 1,8-diaminooctane (DAO)\",\n        \"synthesis_product\": \"large, yellow, rectangular crystals\",\n        \"synthesis_description\": \"First, SnCl2 x 2H2O (450 mg, 2 mmol) was added to a 57% w/w aqueous HI solution (5 mL) and a 50% aqueous H3PO2 solution (8 mL). After constant magnetic stirring at a boiling temperature, 1,8-diaminooctane (DAO) (72 mg, 0.5 mmol) was dissolved, after which the stirring ceased, the solution cooled, and crystals formed after 10 minutes.\",\n        \"experimental_method\": \"UV-vis absorption (diffused reflectance)\",\n        \"experimental_description\": \"A Shimadzu UV-3600 PC double-beam/double monochromator spectrophotometer was used to collect the data. The device was operated between 200 and 2500 nm. The non-absorbing reflectance reference was BaSO4. To find the estimated band gap of the material, the reflectance was converted to absorbance via the Kubelka-Munk equation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1810,\n        \"id\": 445,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) lead bromide\",\n        \"formula\": \"C20H44Br4N2Pb\",\n        \"group\": \"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) lead bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Smart Platform diffractometer with Apex I CCD detector and MoK\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and an Oxford Xcalibur S diffractometer with Sapphire 3 CCD detector and MoK\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) were used.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1811,\n        \"id\": 445,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) lead bromide\",\n        \"formula\": \"C20H44Br4N2Pb\",\n        \"group\": \"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) lead bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Melting Point\",\n        \"primary_unit\": \"\\u00b0C\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",\n        \"experimental_method\": \"Melting point measurement\",\n        \"experimental_description\": \"A BUCHI M-565 Melting point instrument was used to collect data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1813,\n        \"id\": 445,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) lead bromide\",\n        \"formula\": \"C20H44Br4N2Pb\",\n        \"group\": \"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) lead bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1814,\n        \"id\": 445,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) lead bromide\",\n        \"formula\": \"C20H44Br4N2Pb\",\n        \"group\": \"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) lead bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1815,\n        \"id\": 445,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) lead bromide\",\n        \"formula\": \"C20H44Br4N2Pb\",\n        \"group\": \"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) lead bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",\n        \"experimental_method\": \"PLQY\",\n        \"experimental_description\": \"A Quantaurus-QY spectrometer, developed from Hamamatsu, was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1816,\n        \"id\": 445,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) lead bromide\",\n        \"formula\": \"C20H44Br4N2Pb\",\n        \"group\": \"Bmpip2PbBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromoplumbate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) lead bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Stokes shift\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 98%, Acros Organics, 500 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, PbBr2 (36.7 mg, 0.1 mmol) and BmpipBr (0.4 mmol, 94.5 mg) were dissolved in 1 mL of DMF. Then, Et2O was diffused into this solution at room temperature, and crystals began to grow.\",\n        \"experimental_method\": \"Photoluminescence (PL) and PL excitation\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1817,\n        \"id\": 446,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin bromide\",\n        \"formula\": \"C20H44Br4N2Sn\",\n        \"group\": \"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70\\u00baC to room temperature, allowing crystals to grow.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Smart Platform diffractometer with Apex I CCD detector and MoK\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and an Oxford Xcalibur S diffractometer with Sapphire 3 CCD detector and MoK\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) were used.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1818,\n        \"id\": 446,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin bromide\",\n        \"formula\": \"C20H44Br4N2Sn\",\n        \"group\": \"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Melting Point\",\n        \"primary_unit\": \"\\u00b0C\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70\\u00baC to room temperature, allowing crystals to grow.\",\n        \"experimental_method\": \"Melting point measurement\",\n        \"experimental_description\": \"A BUCHI M-565 Melting point instrument was used to collect data.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1819,\n        \"id\": 446,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin bromide\",\n        \"formula\": \"C20H44Br4N2Sn\",\n        \"group\": \"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70\\u00baC to room temperature, allowing crystals to grow.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1820,\n        \"id\": 446,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin bromide\",\n        \"formula\": \"C20H44Br4N2Sn\",\n        \"group\": \"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70\\u00baC to room temperature, allowing crystals to grow.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1821,\n        \"id\": 446,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin bromide\",\n        \"formula\": \"C20H44Br4N2Sn\",\n        \"group\": \"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70\\u00baC to room temperature, allowing crystals to grow.\",\n        \"experimental_method\": \"PLQY measurement\",\n        \"experimental_description\": \"A Quantaurus-QY spectrometer, developed from Hamamatsu, was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1822,\n        \"id\": 446,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin bromide\",\n        \"formula\": \"C20H44Br4N2Sn\",\n        \"group\": \"Bmpip2SnBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnBr4, Tin bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin bromide\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Stokes shift\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) bromide SnBr2,(99.5%, Alfa Aesar, 25 g)),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), DMF(anhydrous, 99.8%, Sigma-Aldrich, 100 ml), Et2O (99.5%, extra dry over molecular sieve, stabilized, AcroSeal, 100 ml)\",\n        \"synthesis_product\": \"Single crystals\",\n        \"synthesis_description\": \"First, SnBr2 (0.4 mmol) and BmpipBr (0.8 mmol) were dissolved in 2 mL of EtOH. The solution was cooled from 70\\u00baC to room temperature, allowing crystals to grow.\",\n        \"experimental_method\": \"Photoluminescence and Photoluminescence excitation\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1823,\n        \"id\": 447,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) germanium bromide\",\n        \"formula\": \"C20H44Br4GeN2\",\n        \"group\": \"Bmpip2GeBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromogermaniate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"GeBr4, Germanium bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) germanium bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"germanium(II) bromide (GeBr2, 97%, Aldrich-Fine Chemicals, 5 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), ethanol, EtOH (anhydrous, 99.8%, Acros Organics, 1 L)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, GeBr2 (0.5 mmol) and BmpipBr (1 mmol) were dissolved in 3 mL of EtOH. Then, 2 mL of Et2O was added to the EtOH solution, and single crystals began to grow at the interface.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker Smart Platform diffractometer with Apex I CCD detector and MoK\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and an Oxford Xcalibur S diffractometer with Sapphire 3 CCD detector and MoK\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) were used.\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1825,\n        \"id\": 447,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) germanium bromide\",\n        \"formula\": \"C20H44Br4GeN2\",\n        \"group\": \"Bmpip2GeBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromogermaniate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"GeBr4, Germanium bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) germanium bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"germanium(II) bromide (GeBr2, 97%, Aldrich-Fine Chemicals, 5 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), ethanol, EtOH (anhydrous, 99.8%, Acros Organics, 1 L)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, GeBr2 (0.5 mmol) and BmpipBr (1 mmol) were dissolved in 3 mL of EtOH. Then, 2 mL of Et2O was added to the EtOH solution, and single crystals began to grow at the interface.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1826,\n        \"id\": 447,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) germanium bromide\",\n        \"formula\": \"C20H44Br4GeN2\",\n        \"group\": \"Bmpip2GeBr4, Bis(1-butyl-1-methyl-piperidinium) tetrabromogermaniate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"GeBr4, Germanium bromide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) germanium bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Stokes shift\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"germanium(II) bromide (GeBr2, 97%, Aldrich-Fine Chemicals, 5 g),1-butyl-1-methylpiperidinium bromide (BmpipBr, >97%, TCI, 5g; 99%, IOLITEC, 50 g), ethanol, EtOH (anhydrous, 99.8%, Acros Organics, 1 L)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, GeBr2 (0.5 mmol) and BmpipBr (1 mmol) were dissolved in 3 mL of EtOH. Then, 2 mL of Et2O was added to the EtOH solution, and single crystals began to grow at the interface.\",\n        \"experimental_method\": \"Photoluminescence and PL excitation\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1827,\n        \"id\": 448,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin iodide\",\n        \"formula\": \"C20H44I4N2Sn\",\n        \"group\": \"Bmpip2SnI4, Bis(1-butyl-1-methyl-piperidinium) tetraiodostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) iodide (99%, Strem Chemicals, 25 g),1-butyl-1-methylpiperidinium iodide, BmpipI (>98%, IOLITEC, 50 g), acetone, \\u03b3-butyrolactone, GBL (99+%, Acros Organics, 1 L)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, SnI2 (1 mmol) and BmpipI (2 mmol) were dissolved in GBL (4 mL). After acetone was added, beige powder resulted. Crystals were grown by cooling stock GBL to room temperature from 90\\u00baC.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1828,\n        \"id\": 448,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin iodide\",\n        \"formula\": \"C20H44I4N2Sn\",\n        \"group\": \"Bmpip2SnI4, Bis(1-butyl-1-methyl-piperidinium) tetraiodostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Stokes shift\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) iodide (99%, Strem Chemicals, 25 g),1-butyl-1-methylpiperidinium iodide, BmpipI (>98%, IOLITEC, 50 g), acetone, \\u03b3-butyrolactone, GBL (99+%, Acros Organics, 1 L)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, SnI2 (1 mmol) and BmpipI (2 mmol) were dissolved in GBL (4 mL). After acetone was added, beige powder resulted. Crystals were grown by cooling stock GBL to room temperature from 90\\u00baC.\",\n        \"experimental_method\": \"Photoluminescence and PL excitation\",\n        \"experimental_description\": \"PL emission and excitation were collected with FluoroMax4-Plus-P (Horiba Jobin Yvon) or Fluorolog 3 (Horiba Jobin Yvon). The FluoroMax4-Plus-P was powered by 150 W, and the Fluorolog 3 was powered by 500 W Xenon lamps. The samples were photoexcited by a 35 ps, 405 nm pulsed diode laser.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b02365\",\n        \"dataset_ID\": 1829,\n        \"id\": 448,\n        \"compound_name\": \"Bis(1-butyl-1-methyl-piperidinium) tin iodide\",\n        \"formula\": \"C20H44I4N2Sn\",\n        \"group\": \"Bmpip2SnI4, Bis(1-butyl-1-methyl-piperidinium) tetraiodostannate(II)\",\n        \"organic\": \"C10H22N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(N-butyl-N-methyl-piperidinium) tin iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Disphenoidal zero-dimensional lead, tin, and germanium halides: highly emissive singlet and triplet self-trapped excitons and X-ray scintillation\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"141\",\n        \"pages_start\": \"9764\",\n        \"pages_end\": \"9768\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"tin(II) iodide (99%, Strem Chemicals, 25 g),1-butyl-1-methylpiperidinium iodide, BmpipI (>98%, IOLITEC, 50 g), acetone, \\u03b3-butyrolactone, GBL (99+%, Acros Organics, 1 L)\",\n        \"synthesis_product\": \"single crystals\",\n        \"synthesis_description\": \"First, SnI2 (1 mmol) and BmpipI (2 mmol) were dissolved in GBL (4 mL). After acetone was added, beige powder resulted. Crystals were grown by cooling stock GBL to room temperature from 90\\u00baC.\",\n        \"experimental_method\": \"PLQY measurements\",\n        \"experimental_description\": \"A Quantaurus-QY spectrometer, developed from Hamamatsu, was used.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1831,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \": First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Saturn 724 diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Crystal structures were solved by direct methods and refined with the SHELXLTL software.\",\n        \"physical_property\": \"203.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"CCDC database\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1832,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Saturn 724 diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Crystal structures were solved by direct methods and refined with the SHELXLTL software.\",\n        \"physical_property\": \"328.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pnma\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1833,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Rigaku Saturn 724 diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) was used. Crystal structures were solved by direct methods and refined with the SHELXLTL software.\",\n        \"physical_property\": \"363.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P63/m\",\n        \"extraction_method\": \"CCDC database\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1834,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition behavior\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Differential scanning calorimetry (DSC)\",\n        \"experimental_description\": \"PerkinElmer Diamond DSC instrument\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1835,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"phase transition behavior\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Differential scanning calorimetry (DSC)\",\n        \"experimental_description\": \"PerkinElmer Diamond DSC instrument\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1836,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Melting Point\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1837,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"TGA\",\n        \"experimental_description\": \"A TG209 F3 instrument was used at a heating rate of 10 K per minute.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1838,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"An Edinburgh FLS1000 Spectrometer was used to collect data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1839,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"counts\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"An Edinburgh FLS1000 Spectrometer was used to collect data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.0c03008\",\n        \"dataset_ID\": 1840,\n        \"id\": 449,\n        \"compound_name\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"formula\": \"[(CH3)3PCH2F]CdCl2Br\",\n        \"group\": \"Trimethyl(fluoromethyl)phosphonium monobromo dichlorocadmiate(II)\",\n        \"organic\": \"C4H11PF\",\n        \"inorganic\": \"CdCl2Br, Cadmium bromide chloride\",\n        \"iupac\": \"Trimethyl(fluoromethyl)phosphonium cadmium bromide chloride\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"dielectric permittivity\",\n        \"primary_unit\": \"F/m\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"pellet\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phosphonium-Based One-Dimensional Perovskite with Switchable Dielectric Behaviors and Phase Transitions\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"59\",\n        \"pages_start\": \"18396\",\n        \"pages_end\": \"18401\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"fluorobromomethane, trimethylphosphine, acetonitrile, CdCl2\",\n        \"synthesis_product\": \"rod-like crystals\",\n        \"synthesis_description\": \"First, [(CH3)3PCH2F]Br was synthesized by mixing fluorobromomethane (2.566 mL, 40 mmol) and trimethylphosphine (4 mL, 40 mmol) in anhydrous acetonitrile (50 mL). After the solution was stirred at 313 K for 5 hours and cooled, the salt was collected for stage two of the synthesis. CdCl2 (4 mmol, 0.7332 g) and the as-synthesized [(CH3)3PCH2F]Br (4 mmol, 0.7560 g) were combined to form a methanol solution (50 mL), which then evaporated at room temperature for approximately 7 days.\",\n        \"experimental_method\": \"Dielectric\",\n        \"experimental_description\": \"A Tonghui TH2828A was used between temperatures 200 to 400 K at 1 MHz with AC voltage of 1 V to find the dielectric constant.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"Heating\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1016/j.jallcom.2020.156790\",\n        \"dataset_ID\": 1841,\n        \"id\": 450,\n        \"compound_name\": \"Calcium tin sulfide\",\n        \"formula\": \"CaSnS3\",\n        \"group\": \"Calcium trisulfostannate(II), CaSnS3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnS3\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of the Sn-based CaSnS3 chalcogenide perovskite thin film as a highly stable photoabsorber for optoelectronic applications\",\n        \"journal\": \"Alloys and compounds\",\n        \"vol\": \"851\",\n        \"pages_start\": \"253\",\n        \"pages_end\": \"265\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/acsmaterialslett.9b00102\",\n        \"dataset_ID\": 1846,\n        \"id\": 85,\n        \"compound_name\": \"Bis(perfluorophenethylammonium) lead iodide\",\n        \"formula\": \"C32H38F2N4Pb2I8\",\n        \"group\": \"bis(2-(perfluorophenyl)ethan-1-aminium) octoiodo diplumbate(II), (F[5]-PEA)2PbI4\",\n        \"organic\": \"C8H7F5N\",\n        \"inorganic\": \"Pb2I8, Lead iodide\",\n        \"iupac\": \"bis(2-(perfluorophenyl)ethan-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-14\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Aryl-Perfluoroaryl Interaction in TwoDimensional Organic\\u2212Inorganic Hybrid Perovskites Boosts Stability and Photovoltaic Efficiency\",\n        \"journal\": \"ACS Materials Letters\",\n        \"vol\": \"1\",\n        \"pages_start\": \"171\",\n        \"pages_end\": \"176\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/solr.201900374\",\n        \"dataset_ID\": 1847,\n        \"id\": 452,\n        \"compound_name\": \"Propylammonium iodide\",\n        \"formula\": \"CH3(CH2)2NH3I\",\n        \"group\": \"C3AI\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"I, iodide\",\n        \"iupac\": \"propylaminium iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhancing Photovoltaic Performance of Aromatic Ammonium\\u2010based Two\\u2010Dimensional Organic\\u2010Inorganic Hybrid Perovskites via Tuning CH\\u00b7\\u00b7\\u00b7\\u03c0 Interaction\",\n        \"journal\": \"Wiley Online Library\",\n        \"vol\": \"4\",\n        \"pages_start\": \"10\",\n        \"pages_end\": \"30\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"n-propylamine with hydriodic acid (HI) (57wt% in water)\",\n        \"synthesis_product\": \"CH3(CH2)2NH3I (C3AI)\",\n        \"synthesis_description\": \"C3AI was synthesized by evaporating a mixture of n-propylamine with hydriodic acid at 0 \\u00b0C and recrystallizing the product in ethanol.3\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/solr.201900374\",\n        \"dataset_ID\": 1848,\n        \"id\": 452,\n        \"compound_name\": \"Propylammonium iodide\",\n        \"formula\": \"CH3(CH2)2NH3I\",\n        \"group\": \"C3AI\",\n        \"organic\": \"C3NH10\",\n        \"inorganic\": \"I, iodide\",\n        \"iupac\": \"propylaminium iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Enhancing Photovoltaic Performance of Aromatic Ammonium\\u2010based Two\\u2010Dimensional Organic\\u2010Inorganic Hybrid Perovskites via Tuning CH\\u00b7\\u00b7\\u00b7\\u03c0 Interaction\",\n        \"journal\": \"Wiley Online Library\",\n        \"vol\": \"4\",\n        \"pages_start\": \"10\",\n        \"pages_end\": \"30\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03208\",\n        \"dataset_ID\": 1849,\n        \"id\": 33,\n        \"compound_name\": \"Bis(aminoethyl)-bithiophene lead iodide\",\n        \"formula\": \"C12H18N2S2PbI4\",\n        \"group\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene tetraiodoplumbate(II), AE2TPbI4, (AEDT)PbI4, AEDTPbI4, C12H18S2N2PbI4\",\n        \"organic\": \"C12H18N2S2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"5,5'-bis(aminoethyl)-2,2'-bithiophene lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Resolving Rotational Stacking Disorder and Electronic Level Alignment in a 2D Oligothiophene-Based Lead Iodide Perovskite\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"8523\",\n        \"pages_end\": \"8532\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"AE2T\\u00b7HI, PbI2, HI, dimethylformamide\",\n        \"synthesis_product\": \"red crystals\",\n        \"synthesis_description\": \"First, a solution of PbI2 (3.7 mg) and AE2T\\u00b7HI (4 mg) was cooled in 2 mL of aqueous HI (57 wt% in H2O, stabilized) and 0.6 mL of dimethylformamide in N2 atmosphere. The solution started from a temperature of 105\\u00ba C and cooled to room temperature over a time period of 60 hours.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"A Bruker APEX II CCD diffractometer at settings 50 kV and 30 mA with MoK\\u03b1 radiation (\\u03bb = 0.710 \\u00c5) was used to collect data. SAINT program was used to integrate data, and SADABS program was used to correct the absorption.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1850,\n        \"id\": 453,\n        \"compound_name\": \"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO \",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"S-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"A Bruker D8 ADVANCE Series II (MoK\\u03b1 radiation) was used to to collect data at room temperature. Structures were then solved and refined through the Shelxl and Olex software.\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1851,\n        \"id\": 453,\n        \"compound_name\": \"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO \",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Infrared absorption spectrum\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"S-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"infrared absorption\",\n        \"experimental_description\": \"A Bruker VERTEX70 unit was used to collect data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1852,\n        \"id\": 453,\n        \"compound_name\": \"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO \",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"S-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 spectrophotometer was used to collect measurements. Diffuse reflectance data were converted to optical absorption via the Kubelka-Munk equation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1853,\n        \"id\": 453,\n        \"compound_name\": \"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO \",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"S-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba Jobi-Yvon LabRAM ARAMIS system was used to collect data at room temperature. The sample was excited with a 325nm He-Cd laser, focused through a 40x UV objective.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1854,\n        \"id\": 453,\n        \"compound_name\": \"Bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(S)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO \",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((S)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"S-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of S-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"Thermogravimetric Analysis\",\n        \"experimental_description\": \"A NETZSCH-STA-449F3 was used to collect data when the sample was in a dry nitrogen atmosphere.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1855,\n        \"id\": 454,\n        \"compound_name\": \"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO\",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"R-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"Single Crystal X-ray Diffraction\",\n        \"experimental_description\": \"A Bruker D8 ADVANCE Series II (MoK\\u03b1 radiation) was used to to collect data at room temperature. Structures were then solved and refined through the Shelxl and Olex software.\",\n        \"physical_property\": \"296.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1856,\n        \"id\": 454,\n        \"compound_name\": \"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO\",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"R-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"A Shimadzu UV-3600 spectrophotometer was used to collect measurements. Diffuse reflectance data were converted to optical absorption via the Kubelka-Munk equation.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1857,\n        \"id\": 454,\n        \"compound_name\": \"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO\",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"R-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"A Horiba Jobi-Yvon LabRAM ARAMIS system was used to collect data at room temperature. The sample was excited with a 325nm He-Cd laser, focused through a 40x UV objective.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1858,\n        \"id\": 454,\n        \"compound_name\": \"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO\",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Infrared absorption spectrum\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"wavenumber\",\n        \"secondary_unit\": \"cm^{-1}\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"R-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"infrared absorption\",\n        \"experimental_description\": \"A Bruker VERTEX70 unit was used to collect data.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1016/j.poly.2018.11.026\",\n        \"dataset_ID\": 1859,\n        \"id\": 454,\n        \"compound_name\": \"Bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead chloride\",\n        \"formula\": \"C30H42Cl10O2Pb4\",\n        \"group\": \"(R)-1-(1-naphthyl)ethy-lamineH)2[Pb4Cl10] \\u201a\\u00c4\\u00a2 2DMF, bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide decachloro tetraplumbate(II)\",\n        \"organic\": \"C12H14N, C3H7NO\",\n        \"inorganic\": \"Pb4Cl10, Lead chloride\",\n        \"iupac\": \"bis((R)-1-(1-naphthyl)ethylamineH) N,N-dimethylformamide lead (II) chloride\",\n        \"last_update\": \"2022-08-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Stereochemically active lead chloride enantiomers mediated by homochiral organic cation\",\n        \"journal\": \"Polyhedron\",\n        \"vol\": \"158\",\n        \"pages_start\": \"445\",\n        \"pages_end\": \"448\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"R-NEA, PbCl2, DMF, 2-butanol\",\n        \"synthesis_product\": \"clear crystals\",\n        \"synthesis_description\": \"First, a mixture of R-NEA (17.1 mg, 0.010 mmol) and PbCl2 (13.9 mg, 0.005 mmol) was created, and this mixture was weighted in a 4 mL scintillation vial. Next, the mixture was dissolved in 0.5 mL DMF solvent, after which 1 mL of 2-butanol was added on top of the DMF solution. Over a span of months, the solvents evaporated, and clear crystals resulted.\",\n        \"experimental_method\": \"Thermogravimetric Analysis\",\n        \"experimental_description\": \"A NETZSCH-STA-449F3 was used to collect data when the sample was in a dry nitrogen atmosphere.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201906571\",\n        \"dataset_ID\": 1860,\n        \"id\": 455,\n        \"compound_name\": \"Bis(phenethylammonium) tris(formamidinium) lead bromide\",\n        \"formula\": \"(PEA)2(FA)3Pb4Br13\",\n        \"group\": \"(PEA)2(FA)3Pb4Br13, bis(phenethylaminium) tris(diaminomethanide) tridecabromo tetraplumbate(II)\",\n        \"organic\": \"C8H12N, CH5N2\",\n        \"inorganic\": \"Pb4Br13, Lead bromide\",\n        \"iupac\": \"bis(phenethylaminium) tris(diaminomethanide) lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient Energy Funneling in Quasi-2D Perovskites: From Light Emission to Lasing.\",\n        \"journal\": \"Advanced materials\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1906571-1\",\n        \"pages_end\": \"1906571-16\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"UV-VIS Spectroscopy\",\n        \"experimental_description\": \"Films of quasi-2D perovskite (PEA)2(FA)3Pb4Br13 were prepared from the DMSO and NMP solvents to measure their absorbance vs wavelength intensity.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"DMSO\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.201906571\",\n        \"dataset_ID\": 1861,\n        \"id\": 455,\n        \"compound_name\": \"Bis(phenethylammonium) tris(formamidinium) lead bromide\",\n        \"formula\": \"(PEA)2(FA)3Pb4Br13\",\n        \"group\": \"(PEA)2(FA)3Pb4Br13, bis(phenethylaminium) tris(diaminomethanide) tridecabromo tetraplumbate(II)\",\n        \"organic\": \"C8H12N, CH5N2\",\n        \"inorganic\": \"Pb4Br13, Lead bromide\",\n        \"iupac\": \"bis(phenethylaminium) tris(diaminomethanide) lead bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"4\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient Energy Funneling in Quasi-2D Perovskites: From Light Emission to Lasing.\",\n        \"journal\": \"Advanced materials\",\n        \"vol\": \"32\",\n        \"pages_start\": \"1906571-1\",\n        \"pages_end\": \"1906571-16\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Optical properties of quasi-2D perovskite (PEA)2(FA)3Pb4Br13 films prepared from solvent DMSO and NMP and were then measured via Photoluminescence to obtain their PL intensity at certain wavelengths.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"DMSO\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.202005868\",\n        \"dataset_ID\": 1864,\n        \"id\": 456,\n        \"compound_name\": \"bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] lead bromide\",\n        \"formula\": \"S-[C10H7CH(CH3)NH3]2PbBr4\",\n        \"group\": \"S-NPB, bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",\n        \"organic\": \"C12NH14\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(S-(\\u2212)-1-(1-naphthyl)ethylammonium) lead (II) bromide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"Chiral 2D bromide perovskite that forms glass on quenching\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1583,\n            1629,\n            1630\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Crystal\\u2013Glass Transition in a Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2005868\",\n        \"pages_end\": \"2005868\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",\n        \"synthesis_product\": \"[S-(\\u2212)-1-(1-naphthyl)ethylammonium]2PbBr4\",\n        \"synthesis_description\": \"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(\\u2212)-1-\\r\\n(1-naphthyl)ethylamine (78 \\u00b5L, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 \\u00b0C. The hot solution was slowly cooled to room temperature (21  \\u00b0C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry\",\n        \"experimental_description\": \"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 \\u00b0C; enthalpy of melting: 28.71 J g\\u22121), which upon repeating the experiment showed an acceptable temperature offset of 0.2  \\u00b0C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 \\u00b0C min\\u22121. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (\\u22485.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  \\u00b0C at a ramp rate of 5  \\u00b0C min\\u22121. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (\\u22485.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5\\u00b0C min\\u22121 over a temperature range from 25 to 185 \\u00b0C and heated isothermally at 185 \\u00b0C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  \\u00b0C min\\u22121. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g\\u22121)/ramp rate (\\u00b0C s\\u22121) and temperature.\\r\\n\\r\\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 \\u00b0C min\\u22121 ramping rate from 25 to 300 \\u00b0C under nitrogen gas flow (40 mL min\\u22121) with samples (\\u22484.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\",\n        \"physical_property\": \"175.0\",\n        \"unit\": \"\\u00b0C\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21\",\n        \"extraction_method\": \"Manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.202005868\",\n        \"dataset_ID\": 1866,\n        \"id\": 456,\n        \"compound_name\": \"bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] lead bromide\",\n        \"formula\": \"S-[C10H7CH(CH3)NH3]2PbBr4\",\n        \"group\": \"S-NPB, bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",\n        \"organic\": \"C12NH14\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(S-(\\u2212)-1-(1-naphthyl)ethylammonium) lead (II) bromide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"Chiral 2D bromide perovskite that forms glass on quenching\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"thermal transition behavior\",\n        \"primary_unit\": \"W/g\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Crystal\\u2013Glass Transition in a Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2005868\",\n        \"pages_end\": \"2005868\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",\n        \"synthesis_product\": \"[S-(\\u2212)-1-(1-naphthyl)ethylammonium]2PbBr4\",\n        \"synthesis_description\": \"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(\\u2212)-1-\\r\\n(1-naphthyl)ethylamine (78 \\u00b5L, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 \\u00b0C. The hot solution was slowly cooled to room temperature (21  \\u00b0C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry\",\n        \"experimental_description\": \"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 \\u00b0C; enthalpy of melting: 28.71 J g\\u22121), which upon repeating the experiment showed an acceptable temperature offset of 0.2  \\u00b0C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 \\u00b0C min\\u22121. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (\\u22485.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  \\u00b0C at a ramp rate of 5  \\u00b0C min\\u22121. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (\\u22485.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5\\u00b0C min\\u22121 over a temperature range from 25 to 185 \\u00b0C and heated isothermally at 185 \\u00b0C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  \\u00b0C min\\u22121. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g\\u22121)/ramp rate (\\u00b0C s\\u22121) and temperature.\\r\\n\\r\\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 \\u00b0C min\\u22121 ramping rate from 25 to 300 \\u00b0C under nitrogen gas flow (40 mL min\\u22121) with samples (\\u22484.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.202005868\",\n        \"dataset_ID\": 1868,\n        \"id\": 456,\n        \"compound_name\": \"bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] lead bromide\",\n        \"formula\": \"S-[C10H7CH(CH3)NH3]2PbBr4\",\n        \"group\": \"S-NPB, bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",\n        \"organic\": \"C12NH14\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(S-(\\u2212)-1-(1-naphthyl)ethylammonium) lead (II) bromide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"Chiral 2D bromide perovskite that forms glass on quenching\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Glass transition temperature\",\n        \"primary_unit\": \"W/g\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Crystal\\u2013Glass Transition in a Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2005868\",\n        \"pages_end\": \"2005868\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",\n        \"synthesis_product\": \"[S-(\\u2212)-1-(1-naphthyl)ethylammonium]2PbBr4\",\n        \"synthesis_description\": \"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(\\u2212)-1-\\r\\n(1-naphthyl)ethylamine (78 \\u00b5L, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 \\u00b0C. The hot solution was slowly cooled to room temperature (21  \\u00b0C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry\",\n        \"experimental_description\": \"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 \\u00b0C; enthalpy of melting: 28.71 J g\\u22121), which upon repeating the experiment showed an acceptable temperature offset of 0.2  \\u00b0C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 \\u00b0C min\\u22121. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (\\u22485.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  \\u00b0C at a ramp rate of 5  \\u00b0C min\\u22121. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (\\u22485.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5\\u00b0C min\\u22121 over a temperature range from 25 to 185 \\u00b0C and heated isothermally at 185 \\u00b0C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  \\u00b0C min\\u22121. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g\\u22121)/ramp rate (\\u00b0C s\\u22121) and temperature.\\r\\n\\r\\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 \\u00b0C min\\u22121 ramping rate from 25 to 300 \\u00b0C under nitrogen gas flow (40 mL min\\u22121) with samples (\\u22484.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.202005868\",\n        \"dataset_ID\": 1869,\n        \"id\": 456,\n        \"compound_name\": \"bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] lead bromide\",\n        \"formula\": \"S-[C10H7CH(CH3)NH3]2PbBr4\",\n        \"group\": \"S-NPB, bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",\n        \"organic\": \"C12NH14\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(S-(\\u2212)-1-(1-naphthyl)ethylammonium) lead (II) bromide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"Chiral 2D bromide perovskite that forms glass on quenching\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"differential scanning calorimetry\",\n        \"primary_unit\": \"W/g\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Crystal\\u2013Glass Transition in a Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2005868\",\n        \"pages_end\": \"2005868\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",\n        \"synthesis_product\": \"[S-(\\u2212)-1-(1-naphthyl)ethylammonium]2PbBr4\",\n        \"synthesis_description\": \"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(\\u2212)-1-\\r\\n(1-naphthyl)ethylamine (78 \\u00b5L, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 \\u00b0C. The hot solution was slowly cooled to room temperature (21  \\u00b0C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry\",\n        \"experimental_description\": \"DSC: Differential Scanning Calorimetry: DSC measurements were performed using a TA Discovery DSC instrument using various ramping rates and temperature ranges (as described in the main text) using a hermetically sealed aluminum pan and lid. Prior to experiments, the DSC setup was calibrated with metallic indium (melting temperature: 156.6 \\u00b0C; enthalpy of melting: 28.71 J g\\u22121), which upon repeating the experiment showed an acceptable temperature offset of 0.2  \\u00b0C and melting enthalpy offset of 0.04%. Calibration and the above measurement were carried out at a ramp rate of 5 \\u00b0C min\\u22121. DSC analyses of crystalline S-NPB and rac-NPB perovskites were carried out by hermetically sealing corresponding crystals (\\u22485.0 mg) in aluminum pan/lid, and ramping temperature from 25 to 250  \\u00b0C at a ramp rate of 5  \\u00b0C min\\u22121. For measurement of S-NPB and R-NPB glasses, samples were prepared by melting S-/R-NPB crystals (\\u22485.0  mg) in an open aluminum pan and quickly placing it on a metallic steel bench to quench to room temperature. After hermetic sealing, the glassy samples were exposed to a heating cycle with ramp rates of  5\\u00b0C min\\u22121 over a temperature range from 25 to 185 \\u00b0C and heated isothermally at 185 \\u00b0C for a minute, before cooling back to room temperature at ramp rates of 1, 5, and 20  \\u00b0C min\\u22121. Since the glass transition occurred over a temperature range, the Tg was determined using the midpoint halfheight method. The Tx, Tm, and Td temperatures were calculated using the intersection between the corresponding DSC peak onset with its horizontal baseline. For Tm, the onset temperature signifies the melting temperature of the sample under consideration, whereas the peak temperature corresponds to complete melting of the sample inside the apparatus. The enthalpy of crystallization and melting were calculated by measuring the area under the curve relating heat flow (W g\\u22121)/ramp rate (\\u00b0C s\\u22121) and temperature.\\r\\n\\r\\nThermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 \\u00b0C min\\u22121 ramping rate from 25 to 300 \\u00b0C under nitrogen gas flow (40 mL min\\u22121) with samples (\\u22484.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.202005868\",\n        \"dataset_ID\": 1870,\n        \"id\": 456,\n        \"compound_name\": \"bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] lead bromide\",\n        \"formula\": \"S-[C10H7CH(CH3)NH3]2PbBr4\",\n        \"group\": \"S-NPB, bis[S-(\\u2212)-1-(1-naphthyl)ethylammonium] tetrabromoplumbate(II), (S-NEA)2PbBr4\",\n        \"organic\": \"C12NH14\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(S-(\\u2212)-1-(1-naphthyl)ethylammonium) lead (II) bromide\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"Chiral 2D bromide perovskite that forms glass on quenching\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"unknown\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Crystal\\u2013Glass Transition in a Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2005868\",\n        \"pages_end\": \"2005868\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-1-(1-naphthyl)ethylamine (>99%, Sigma Aldrich), lead bromide (PbBr2, 99.99%, TCI chemicals) , and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",\n        \"synthesis_product\": \"[S-(\\u2212)-1-(1-naphthyl)ethylammonium]2PbBr4\",\n        \"synthesis_description\": \"To grow S-NPB perovskite crystals, stoichiometric amounts of PbBr2 (90  mg, 0.24  mmol) and (S)-(\\u2212)-1-\\r\\n(1-naphthyl)ethylamine (78 \\u00b5L, 0.48  mmol) were dissolved in aq. HBr (1.0 mL) and deionized water (2.4 mL) in a sealed vial at 95 \\u00b0C. The hot solution was slowly cooled to room temperature (21  \\u00b0C) over a period of 24 h in a water bath, resulting in the formation of colorless plate-like S-NPB single crystals.\",\n        \"experimental_method\": \"Thermogravimetric Analysis\",\n        \"experimental_description\": \"Thermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 \\u00b0C min\\u22121 ramping rate from 25 to 300 \\u00b0C under nitrogen gas flow (40 mL min\\u22121) with samples (\\u22484.5 mg) of single crystals of S-NPB and rac-NPB perovskite. Glassy S-NPB perovskite sample (3.9 mg) for TGA measurement was prepared by scratching off the melt-quenched glass prepared on soda lime glass substrates.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.202005868\",\n        \"dataset_ID\": 1871,\n        \"id\": 408,\n        \"compound_name\": \"1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Melting Point\",\n        \"primary_unit\": \"W/g\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Crystal\\u2013Glass Transition in a Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2005868\",\n        \"pages_end\": \"2005868\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"1-(1-naphthyl) ethylamine (98%, Sigma Aldrich),  lead bromide (PbBr2, 99.99%, TCI chemicals) and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",\n        \"synthesis_product\": \"1-(1-naphthyl)ethylammonium]2PbBr4\",\n        \"synthesis_description\": \"To grow rac-NPB perovskite crystals,\\r\\nstoichiometric amounts of PbBr2 (90 mg, 0.24 mmol) and 1-(1-naphthyl)\\r\\nethylamine (78 \\u00b5L, 0.48 mmol) were dissolved in aq. HBr (1.0 mL) and\\r\\nmethanol (2.4 mL) in a sealed vial at 95 \\u00b0C. The hot solution was slowly\\r\\ncooled to room temperature (21  \\u00b0C) over a period of 24 h in a water\\r\\nbath, resulting in the formation of layered flakes of transparent rac-NPB\\r\\nsingle crystals.\",\n        \"experimental_method\": \"Differential Scanning Calorimetry\",\n        \"experimental_description\": \"Differential Scanning Calorimetry: DSC measurements were performed\\r\\nusing a TA Discovery DSC instrument using various ramping rates and\\r\\ntemperature ranges (as described in the main text) using a hermetically\\r\\nsealed aluminum pan and lid. Prior to experiments, the DSC setup was\\r\\ncalibrated with metallic indium (melting temperature: 156.6 \\u00b0C; enthalpy\\r\\nof melting: 28.71 J g\\u22121\\r\\n), which upon repeating the experiment showed\\r\\nan acceptable temperature offset of 0.2  \\u00b0C and melting enthalpy offset\\r\\nof 0.04%. Calibration and the above measurement were carried out at a\\r\\nramp rate of 5 \\u00b0C min\\u22121\\r\\n. DSC analyses of crystalline S-NPB and rac-NPB\\r\\nperovskites were carried out by hermetically sealing corresponding\\r\\ncrystals (\\u22485.0 mg) in aluminum pan/lid, and ramping temperature from\\r\\n25 to 250  \\u00b0C at a ramp rate of 5  \\u00b0C min\\u22121.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21c\",\n        \"extraction_method\": \"Manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/adma.202005868\",\n        \"dataset_ID\": 1872,\n        \"id\": 408,\n        \"compound_name\": \"1-(1-naphthyl)ethylammonium lead bromide\",\n        \"formula\": \"C24H28N2PbBr4\",\n        \"group\": \"NEA2PbBr4, 1-1-NEA2PbBr4, racemic-NEA2PbBr4, 1-(1-naphthyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C12H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(1-naphthyl)ethanaminium lead (II) bromide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Reversible Crystal\\u2013Glass Transition in a Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2005868\",\n        \"pages_end\": \"2005868\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"1-(1-naphthyl) ethylamine (98%, Sigma Aldrich),  lead bromide (PbBr2, 99.99%, TCI chemicals) and hydrobromic acid (HBr) (48 wt% in H2O, >99.99%, Sigma Aldrich)\",\n        \"synthesis_product\": \"1-(1-naphthyl)ethylammonium]2PbBr4\",\n        \"synthesis_description\": \"To grow rac-NPB perovskite crystals,\\r\\nstoichiometric amounts of PbBr2 (90 mg, 0.24 mmol) and 1-(1-naphthyl)\\r\\nethylamine (78 \\u00b5L, 0.48 mmol) were dissolved in aq. HBr (1.0 mL) and\\r\\nmethanol (2.4 mL) in a sealed vial at 95 \\u00b0C. The hot solution was slowly\\r\\ncooled to room temperature (21  \\u00b0C) over a period of 24 h in a water\\r\\nbath, resulting in the formation of layered flakes of transparent rac-NPB\\r\\nsingle crystals.\",\n        \"experimental_method\": \"Thermogravimetric Analysis\",\n        \"experimental_description\": \"Thermogravimetric Analysis: TGA measurements were performed on a TA Q50 instrument using a 5 \\u00b0C min\\u22121 ramping rate from 25 to 300 \\u00b0C under nitrogen gas flow (40 mL min\\u22121) with samples (\\u22484.5 mg) of single crystals of S-NPB and rac-NPB perovskite.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P21c\",\n        \"extraction_method\": \"Manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1873,\n        \"id\": 282,\n        \"compound_name\": \"3-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(3AMPY)Pb2I6, 3-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2022-06-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA with revPBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"Spin-orbit coupling\",\n        \"basis_set_definition\": \"Core electrons: Troullier\\u2212Martins pseudopotentials; valence electrons are described by double-\\u03b6 polarized basis set with finite numerical pseudoatomic orbitals\",\n        \"numerical_accuracy\": \"Energy cutoff = 150 Ry\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1874,\n        \"id\": 284,\n        \"compound_name\": \"3-aminomethylpyridinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(3AMPY)Sn2I6, 3-(methanaminium)pyridinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA with revPBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"Spin-orbit coupling\",\n        \"basis_set_definition\": \"Core electrons: Troullier\\u2212Martins pseudopotentials; valence electrons are described by double-\\u03b6 polarized basis set with finite numerical pseudoatomic orbitals\",\n        \"numerical_accuracy\": \"Energy cutoff = 150 Ry\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1875,\n        \"id\": 283,\n        \"compound_name\": \"4-aminomethylpyridinium lead iodide\",\n        \"formula\": \"C6H10I6N2Pb2\",\n        \"group\": \"(4AMPY)Pb2I6, 4-(methanaminium)pyridinium hexaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Pb2I6, Lead iodide\",\n        \"iupac\": \"4-(methanaminium)pyridinium lead iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA with revPBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"Spin-orbit coupling\",\n        \"basis_set_definition\": \"Core electrons: Troullier\\u2212Martins pseudopotentials; valence electrons are described by double-\\u03b6 polarized basis set with finite numerical pseudoatomic orbitals\",\n        \"numerical_accuracy\": \"Energy cutoff = 150 Ry\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Ia\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 1876,\n        \"id\": 286,\n        \"compound_name\": \"4-(aminomethyl)piperidinium tin iodide\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"(4AMPY)Sn2I6, 4-(methanaminium)piperidinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"4-(methanaminium)piperidinium tin iodide\",\n        \"last_update\": \"2021-11-30\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"SIESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"GGA with revPBE\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"Spin-orbit coupling\",\n        \"basis_set_definition\": \"Core electrons: Troullier\\u2212Martins pseudopotentials; valence electrons are described by double-\\u03b6 polarized basis set with finite numerical pseudoatomic orbitals\",\n        \"numerical_accuracy\": \"Energy cutoff = 150 Ry\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1039/D1TA03325E\",\n        \"dataset_ID\": 1877,\n        \"id\": 457,\n        \"compound_name\": \"[(NDIC2)2Pb5I14(DMF)2]\\u00b74DMF\",\n        \"formula\": \"C13.5H19.5I3.5N3.5O3.50Pb1.25\",\n        \"group\": \"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone triiodoplumbate(II)\",\n        \"organic\": \"C13.50H19.5\",\n        \"inorganic\": \"I3.5N3.5O3.50Pb1.25\",\n        \"iupac\": \"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Charge Transfer States and Carrier Generation in 1D Organolead Iodide Semiconductors\",\n        \"journal\": \"The Royal Society of Chemistry\",\n        \"vol\": \"1111\",\n        \"pages_start\": \"1\",\n        \"pages_end\": \"16\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"NDIC2, Pb2I6, DMF,\",\n        \"synthesis_product\": \"[(NDIC2)2Pb5I14(DMF)2]\\u00b74DMF\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Absorption Spectrum\",\n        \"experimental_description\": \"NDIC2-I2 was dissolved in DMF and the solution-phase optical absorption spectrum was measured.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-I\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1039/D1TA03325E\",\n        \"dataset_ID\": 1878,\n        \"id\": 457,\n        \"compound_name\": \"[(NDIC2)2Pb5I14(DMF)2]\\u00b74DMF\",\n        \"formula\": \"C13.5H19.5I3.5N3.5O3.50Pb1.25\",\n        \"group\": \"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone triiodoplumbate(II)\",\n        \"organic\": \"C13.50H19.5\",\n        \"inorganic\": \"I3.5N3.5O3.50Pb1.25\",\n        \"iupac\": \"2,7-bis(2-ammoniumethyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone iodide\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Charge Transfer States and Carrier Generation in 1D Organolead Iodide Semiconductors\",\n        \"journal\": \"The Royal Society of Chemistry\",\n        \"vol\": \"1111\",\n        \"pages_start\": \"1\",\n        \"pages_end\": \"16\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Temperature-dependent PL emission spectra\",\n        \"experimental_description\": \"The organic-inorganic compounds, (NDIC2)Pb2I , PL emission spectra was measured at 5 different temperatures in kelvin (e.g 5 K, 10 K, 20 K, 40 K, 80 K). After measuring the intensities at those wavelengths, they were analyzed on a intensity vs temperature graph.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"509 nm\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-021-25149-7\",\n        \"dataset_ID\": 1879,\n        \"id\": 458,\n        \"compound_name\": \"R-4-Cl-MBA2PbBr4\",\n        \"formula\": \"(C8H11ClN)2PbBr4\",\n        \"group\": \"(R)-4-chloro-\\u0152\\u00b1-methylbenzylammonium lead bromide, (R)-1-(4-chlorophenyl)ethylammonium lead bromide, (R)-1-(4-chlorophenyl)ethylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C8H11ClN\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"None\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"2D chiral perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural descriptor for enhanced spin-splitting in 2D hybrid perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"12\",\n        \"pages_start\": \"4982-1\",\n        \"pages_end\": \"4982-10\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(R)-4-chloro-a-methylbenzylamine (97%), PbBr2, Aq. HBr (48 wt.% in H2O, \\u2265 99.99%)\",\n        \"synthesis_product\": \"R-4-Cl-MBA2PbBr4\",\n        \"synthesis_description\": \"Plate-like, colorless crystals were grown by slowly cooling a hot Aq. HBr solution of 0.122 mol of PbBr2 and 0.244 mmol of organic amine from 95\\u00baC to room temperature over 60 hours. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and an X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P212121\",\n        \"extraction_method\": \"manually added by the author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-021-25149-7\",\n        \"dataset_ID\": 1880,\n        \"id\": 459,\n        \"compound_name\": \"S-1-Me-HA2PbI4\",\n        \"formula\": \"(C7H18N)2PbI4\",\n        \"group\": \"(S)-1-methylhexylammonium lead iodide, (S)-1-methylhexylammonium tetraiodoplumbate(II)\",\n        \"organic\": \"C7H18N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"None\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"2D chiral perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural descriptor for enhanced spin-splitting in 2D hybrid perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"12\",\n        \"pages_start\": \"4982-1\",\n        \"pages_end\": \"4982-10\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(S)-(+)-1-methyl hexylamine or (S)-(+)-2-Aminoheptane (99%), PbI2, Aq. HI (57 wt. % in H2O, distilled, stabilized, 99.95%)\",\n        \"synthesis_product\": \"S-1-Me-HA2PbI4\",\n        \"synthesis_description\": \"Orange crystals were grown by slowly cooling a hot Aq. HI solution of 0.122 mol of PbI2 and 0.244 mmol of organic amine from 95\\u00baC to room temperature over 60 hours. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and an X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P 21 21 21\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-021-25149-7\",\n        \"dataset_ID\": 1881,\n        \"id\": 460,\n        \"compound_name\": \"S-2-Me-BuA2PbBr4\",\n        \"formula\": \"(C5H14N)2PbBr4\",\n        \"group\": \"(S)-2-methylbutylammonium lead bromide, (S)-2-methylbutylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"None\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"2D chiral perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural descriptor for enhanced spin-splitting in 2D hybrid perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"12\",\n        \"pages_start\": \"4982-1\",\n        \"pages_end\": \"4982-10\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-2-Methylbutylamine (95%), PbBr2, Aq. HBr (48 wt.% in H2O, \\u2265 99.99%)\",\n        \"synthesis_product\": \"S-2-Me-BuA2PbBr4\",\n        \"synthesis_description\": \"Plate-like, colorless crystals were grown by slowly cooling a hot Aq. HBr solution of 0.122 mol of PbBr2 and 0.244 mmol of organic amine from 95\\u00baC to room temperature over 60 hours. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and an X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 21\",\n        \"extraction_method\": \"manually added by the author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-021-25149-7\",\n        \"dataset_ID\": 1882,\n        \"id\": 461,\n        \"compound_name\": \"S-4-NO2-MBA2PbBr4.H2O\",\n        \"formula\": \"(C8H11N2O2)2PbBr4.H2O\",\n        \"group\": \"(S)-\\u0152\\u00b1-Methyl-4-nitrobenzylammonium lead bromide, (S)-4-nitro-\\u0152\\u00b1-methylbenzylammonium lead bromide, (S)-4-nitro-\\u0152\\u00b1-methylbenzylammonium tetrabromoplumbate(II)\",\n        \"organic\": \"C8H11N2O2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"None\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"2D chiral perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural descriptor for enhanced spin-splitting in 2D hybrid perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"12\",\n        \"pages_start\": \"4982-1\",\n        \"pages_end\": \"4982-10\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(S)-\\u03b1-Methyl-4-nitrobenzylamine hydrochloride or (S)-4-nitro-\\u03b1-methylbenzylamine hydrochloride [\\u2018S-4-NO2-MBA\\u2219HCl\\u2019, 97%], PbBr2,  Aq. HBr (48 wt.% in H2O, \\u2265 99.99%)\",\n        \"synthesis_product\": \"S-4-NO2-MBA2PbBr4.H2O\",\n        \"synthesis_description\": \"Plate-like, colorless single-crystals of [S-4-NO2-MBA]2PbBr4 were grown by slowly evaporating a solution of 0.122 mmol of PbBr2 and 0.244 mmol of S-4-NO2-MBA\\u2219HCl in 0.5 ml Aq. HBr and 1.7 ml methanol at room temperature in the ambient atmosphere.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and an X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 21\",\n        \"extraction_method\": \"manually added by the author\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-021-25149-7\",\n        \"dataset_ID\": 1883,\n        \"id\": 462,\n        \"compound_name\": \"S-4-NH3-MBAPbI4\",\n        \"formula\": \"(C8H14N2)PbI4\",\n        \"group\": \"(S)-4-ammonio-\\u0152\\u00b1-methylbenzylammonium lead iodide, (S)-4-ammonio-\\u0152\\u00b1-methylbenzylammonium tetraiodoplumbate(II)\",\n        \"organic\": \"C8H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"None\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"2D chiral perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural descriptor for enhanced spin-splitting in 2D hybrid perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"12\",\n        \"pages_start\": \"4982-1\",\n        \"pages_end\": \"4982-10\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(S)-\\u03b1-Methyl-4-nitrobenzylamine hydrochloride (97%), PbI2, Aq. HI (57 wt. % in H2O, distilled, stabilized, 99.95%), Aq. H3PO2 (50 wt.% in H2O)\",\n        \"synthesis_product\": \"S-4-NH3-MBA2PbI4\",\n        \"synthesis_description\": \"Single-crystals of S-4-NH3-MBAPbI4 were grown by slowly cooling a hot solution of 0.245 mmol of PbI2, and 0.49 mmol of S-4-NO2-MBA\\u2219HCl in 0.2 ml of Aq. HI and 0.1 ml of Aq. H3PO2  from 85\\u00b0C to room temperature over 5 hrs. The as-obtained single-crystals were filtered, washed thoroughly with diethyl ether, and vacuum-dried.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction (XRD) was performed at 298 K on a Rigaku XtaLAB Synergy-S diffractometer using Mo-K\\u03b1 radiation (\\u03bb=0.710 \\u00c5) and an X-ray tube operating at 50 kV and 30 mA.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"P 21 21 21\",\n        \"extraction_method\": \"manually added by the author\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.1c00757\",\n        \"dataset_ID\": 1884,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"Perdew-Burke-Ernzerhof\",\n        \"k_point_grid\": \"4x4x1\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"JTH PAW\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Surface Reconstruction of Halide Perovskites during Post-treatment\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"18\",\n        \"pages_start\": \"6781\",\n        \"pages_end\": \"6786\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"DMF , 33\\u2009mg\\u2009ml\\u22121 MACl ,33\\u2009mg\\u2009mL\\u22121 MAPbBr3 , 889\\u2009mg\\u2009mL\\u22121 FAPbI3,\",\n        \"synthesis_product\": \"FAPbI3\",\n        \"synthesis_description\": \"The FAPbI3 halide perovskites was synthesized via antisolvent quenching method. Specifically, 889\\u2009mg\\u2009mL\\u22121 FAPbI3, 33\\u2009mg\\u2009mL\\u22121 MAPbBr3, and  33\\u2009mg\\u2009ml\\u22121 MACl were dissolved in a mixed polar aprotic solvent between dimethylformamide (DMF) and dimethylsulfoxide (DMSO)  solvent. Diethyl ether (0.2 mL) was then added to the mixture followed by annealing at 150\\u00b0C for 10 min.\",\n        \"experimental_method\": \"Photoluminescence Intensity\",\n        \"experimental_description\": \"PL spectra of the perovskite film, FAPbI3, with treatment of IPA in relation to time (seconds).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1885,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"2*4*4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1886,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"2*4*4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1888,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1533\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"2*4*4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1889,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1534\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"2*4*4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1890,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            227,\n            1900,\n            1902,\n            1905,\n            1906,\n            1907,\n            1908\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41563-018-0081-x\",\n        \"dataset_ID\": 1892,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1894\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Electron\\u2013phonon interaction in efficient perovskite blue emitters\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"17\",\n        \"pages_start\": \"550\",\n        \"pages_end\": \"556\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2, PEABr, DMF, DMSO, Diethyl Ether, Chloroform\",\n        \"synthesis_product\": \"(PEA)2PbBr4 single crystal\",\n        \"synthesis_description\": \"PbBr2 and PEABr with molar ratio of 1:2 were dissolved into a mixed solvent of DMF and DMSO (30-60%) in a 20ml vial. The vial was put in a sealed larger vail with 40 ml antisolvent (diethyl ether or chloroform). After several days at room temperature, single crystal  (PEA)2PbBr4 will be obtianed, which was rinsed with antisolvent for 3 times and dried at vacuum.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A P4 Bruker diffractometer with Bruker SMART 1\\u2009K CCD (charge-coupled device) detector and a rotating anode utilizing Mo KR radiation (\\u03bb\\u2009=\\u20090.710\\u200973\\u2009\\u00c5) was used to measure  SCXRD data. OLEX2 was used to fitting refinement of single-crystal structures.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41563-018-0081-x\",\n        \"dataset_ID\": 1893,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1896,\n            1897,\n            1898,\n            1899\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Electron\\u2013phonon interaction in efficient perovskite blue emitters\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"17\",\n        \"pages_start\": \"550\",\n        \"pages_end\": \"556\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"PbBr2, PEABr, DMF, DMSO, Diethyl Ether, Chloroform\",\n        \"synthesis_product\": \"(PEA)2PbBr4 single crystal\",\n        \"synthesis_description\": \"PbBr2 and PEABr with molar ratio of 1:2 were dissolved into a mixed solvent of DMF and DMSO (30-60%) in a 20ml vial. The vial was put in a sealed larger vail with 40 ml antisolvent (diethyl ether or chloroform). After several days at room temperature, single crystal  (PEA)2PbBr4 will be obtianed, which was rinsed with antisolvent for 3 times and dried at vacuum.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"A P4 Bruker diffractometer with Bruker SMART 1\\u2009K CCD (charge-coupled device) detector and a rotating anode utilizing Mo KR radiation (\\u03bb\\u2009=\\u20090.710\\u200973\\u2009\\u00c5) was used to measure  SCXRD data. OLEX2 was used to fitting refinement of single-crystal structures.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1894,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1892\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Author uploaded data\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1896,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1893,\n            1897,\n            1898,\n            1899\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Author uploaded data\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1897,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1893,\n            1896,\n            1898,\n            1899\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Author uploaded data\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1898,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1893,\n            1896,\n            1897,\n            1899\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Author uploaded data\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1899,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1893,\n            1896,\n            1897,\n            1898\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Original data\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1900,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            227,\n            1890,\n            1902,\n            1905,\n            1906,\n            1907,\n            1908\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"2*4*4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1901,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            225,\n            745,\n            1903,\n            2267,\n            2269\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"atomic ZORA with SOC\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1902,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            227,\n            1890,\n            1900,\n            1905,\n            1906,\n            1907,\n            1908\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1903,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            225,\n            745,\n            1901,\n            2267,\n            2269\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 1904,\n        \"id\": 2,\n        \"compound_name\": \"Bis(phenylethylammonium) lead chloride\",\n        \"formula\": \"C16H24N2PbCl4\",\n        \"group\": \"(PEA)2PbCl4, (C8H12N)2PbCl4, (C6H5C2H4NH3)2PbCl4, bis(2-phenylethane-1-aminium) tetrachloroplumbate(II)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PEA)2PbCl4, (C8H12N)2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PEA)2PbCl4 crystals, DMF, quartz substrates\",\n        \"synthesis_product\": \"Thin film on quartz\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on quartz substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"Engauge Digitizer (Figure S3)\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1905,\n        \"id\": 463,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide bromide\",\n        \"formula\": \"(C6H5C2H4NH3)2Pb(IxBr1-x)4\",\n        \"group\": \"(PEA)2Pb(IxBr1-x)4\",\n        \"organic\": \"C16H24N2\",\n        \"inorganic\": \"Pb(IxBr1-x)4\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) iodide bromide\",\n        \"last_update\": \"2021-10-26\",\n        \"description\": \"mixed halide Br and I with organic molecule PEA 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            227,\n            1890,\n            1900,\n            1902,\n            1906,\n            1907,\n            1908\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1906,\n        \"id\": 463,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide bromide\",\n        \"formula\": \"(C6H5C2H4NH3)2Pb(IxBr1-x)4\",\n        \"group\": \"(PEA)2Pb(IxBr1-x)4\",\n        \"organic\": \"C16H24N2\",\n        \"inorganic\": \"Pb(IxBr1-x)4\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) iodide bromide\",\n        \"last_update\": \"2021-10-26\",\n        \"description\": \"mixed halide Br and I with organic molecule PEA 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            227,\n            1890,\n            1900,\n            1902,\n            1905,\n            1907,\n            1908\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1907,\n        \"id\": 463,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide bromide\",\n        \"formula\": \"(C6H5C2H4NH3)2Pb(IxBr1-x)4\",\n        \"group\": \"(PEA)2Pb(IxBr1-x)4\",\n        \"organic\": \"C16H24N2\",\n        \"inorganic\": \"Pb(IxBr1-x)4\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) iodide bromide\",\n        \"last_update\": \"2021-10-26\",\n        \"description\": \"mixed halide Br and I with organic molecule PEA 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            227,\n            1890,\n            1900,\n            1902,\n            1905,\n            1906,\n            1908\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Manual entry\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"--\",\n        \"dataset_ID\": 1908,\n        \"id\": 463,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide bromide\",\n        \"formula\": \"(C6H5C2H4NH3)2Pb(IxBr1-x)4\",\n        \"group\": \"(PEA)2Pb(IxBr1-x)4\",\n        \"organic\": \"C16H24N2\",\n        \"inorganic\": \"Pb(IxBr1-x)4\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead (II) iodide bromide\",\n        \"last_update\": \"2021-10-26\",\n        \"description\": \"mixed halide Br and I with organic molecule PEA 2D perovskite\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            227,\n            1890,\n            1900,\n            1902,\n            1905,\n            1906,\n            1907\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE (with TS scheme to account for the Van der Waals effect)\",\n        \"k_point_grid\": \"4*4*2\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"tight\",\n        \"numerical_accuracy\": \"force convergence 5e-3 eV/AA\",\n        \"title\": \"Unpublished\",\n        \"journal\": \"--\",\n        \"vol\": \"--\",\n        \"pages_start\": \"--\",\n        \"pages_end\": \"--\",\n        \"year\": \"--\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"Manual entry\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acsami.0c02313\",\n        \"dataset_ID\": 1909,\n        \"id\": 465,\n        \"compound_name\": \"Bis(butylammonium) lead chloride\",\n        \"formula\": \"C4H12N2PbCl4\",\n        \"group\": \"Bis(butylaminium) tetrachloroplumbate(II), (BA)2PbCl4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"*\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Exploring the Factors Affecting the Mechanical Properties of 2D Hybrid Organic\\u2013Inorganic Perovskites\",\n        \"journal\": \"ACS Publications\",\n        \"vol\": \"12\",\n        \"pages_start\": \"20440\",\n        \"pages_end\": \"20447\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbO powder, 57% w/w aqueous HI solution, butylamine, 50% aqueous H3PO2\",\n        \"synthesis_product\": \"orange plate-like crystals\",\n        \"synthesis_description\": \"10 mmol PbO was dissolved in 16 mL HI at boiling temperature by stirring for ~5 min. Separately, 10 mmol butylamine was added to 1.7 mL H3PO2. The two solutions were mixed and the mixture was allowed to cool to room temperature.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using a STOE IPDS II/IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb = 0.710 73 \\u00c5) and operating at 50 kV and 40 Ma or Bruker Molly or Duo instrument with MoK\\u03b1 I\\u03bcS microfocus source (\\u03bb= 0.71073 \\u00c5) with MX Optics.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc21\",\n        \"extraction_method\": \"Manually extracted\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsami.1c20234\",\n        \"dataset_ID\": 1912,\n        \"id\": 467,\n        \"compound_name\": \"Phenethylammonium silver indium bromide\",\n        \"formula\": \"(C6H5(CH2)2NH3)4AgInBr8\",\n        \"group\": \"(PEA)4AgInBr8, tetra(1-phenyl-2-aminoethane) tetrabromoargentate(I) tetrabromoindiate(III)\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"AgInBr8\",\n        \"iupac\": \"tetra(1-phenyl-2-aminoethane) silver indium octabromide\",\n        \"last_update\": \"2022-01-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Decreasing Structural Dimensionality of Double Perovskites for Phase Stabilization toward Efficient X-ray Detection\",\n        \"journal\": \"ACS Applied Materials & Interfaces\",\n        \"vol\": \"13\",\n        \"pages_start\": \"61447\",\n        \"pages_end\": \"61453\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEABr, AgBr, InBr3\",\n        \"synthesis_product\": \"transparent plate-like crystals\",\n        \"synthesis_description\": \"15 ml HBr was added to PEABr (0.777 g), AgBr (0.182 g) and InBr3 (0.341 g). The solution was heated to 90\\u00b0 while being magnetically stirred until clear. The clear solution was cooled at approx. 2\\u00b0/hour until at room temperature.\",\n        \"experimental_method\": \"SCXRD\",\n        \"experimental_description\": \"Single crystal X-ray diffraction using Rigaku Oxford diffractometer, Mo K\\u03b1 Radiation.\",\n        \"physical_property\": \"293.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6mh00053c\",\n        \"dataset_ID\": 1914,\n        \"id\": 468,\n        \"compound_name\": \"Bis(methylammonium) potassium bismuth chloride\",\n        \"formula\": \"CH6N+2KBiCl6\",\n        \"group\": \"Bis(methanaminium) trichlorobismuthate(III) trichloropotassiate(I), (MA)2KBiCl6\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"KBiCl6\",\n        \"iupac\": \"*\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"The synthesis, structure and electronic properties of a lead-free hybrid inorganic\\u2013organic double perovskite (MA)2KBiCl6 (MA = methylammonium)\",\n        \"journal\": \"Materials Horizons\",\n        \"vol\": \"3\",\n        \"pages_start\": \"328\",\n        \"pages_end\": \"332\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"CH3NH3Cl (synthesized by reacting methylamine solution (40 wt% in H2O) and HCl (37% in H2O)), KCl, BiCl3\",\n        \"synthesis_product\": \"crystalline powder\",\n        \"synthesis_description\": \"Hydrothermal synthesis at 423 K with 2.4 mmol CH3NH3Cl, 1.2 mmol KCl and 1.2 mmol BiCl3 in 1 ml HCl acid solution.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Diffraction data were collected using Oxford Gemini E Ultra diffractometer, Mo K\\u03b1 radiation (\\u03bb = 0.71073\\u00c5), equipped with an Eos CCD detector.\",\n        \"physical_property\": \"297.8 (\\u00b10.2)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c6ta05817e\",\n        \"dataset_ID\": 1915,\n        \"id\": 469,\n        \"compound_name\": \"Bis(methylammonium) thallium bismuth bromide\",\n        \"formula\": \"([CH3NH3]+)2TIBiBr6\",\n        \"group\": \"Bis(methanaminium) tribromobismuthate(III) trichlorotantalate(I), (MA)2TIBiBr6\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"TIBiBr6\",\n        \"iupac\": \"*\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Exploring the properties of lead-free hybrid double perovskites using a combined computational-experimental approach\",\n        \"journal\": \"Journals of Materials Chemistry A\",\n        \"vol\": \"4\",\n        \"pages_start\": \"12025\",\n        \"pages_end\": \"12029\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"298.3 (\\u00b10.3)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acsami.1c20234\",\n        \"dataset_ID\": 1916,\n        \"id\": 471,\n        \"compound_name\": \"i-butylammonium silver indium bromide\",\n        \"formula\": \"(CH(CH3)2CH2NH3)4AgInBr8\",\n        \"group\": \"(i-BA)4AgInBr8, tetra(1-amino-2-methylpropane) tetrabromoargentate(I) tetrabromoindiate(III)\",\n        \"organic\": \"C4NH9\",\n        \"inorganic\": \"AgInBr8\",\n        \"iupac\": \"tetra(1-amino-2-methylpropane) silver indium octabromide\",\n        \"last_update\": \"2022-01-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Decreasing Structural Dimensionality of Double Perovskites for Phase Stabilization toward Efficient X-ray Detection\",\n        \"journal\": \"ACS Applied Materials & Interfaces\",\n        \"vol\": \"13\",\n        \"pages_start\": \"61447\",\n        \"pages_end\": \"61453\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"i-BABr, AgBr, InBr3\",\n        \"synthesis_product\": \"transparent plate-like crystals\",\n        \"synthesis_description\": \"3.0 ml HBr was added to i-BABr (0.638 g), AgBr (0.195 g), and InBr3 (0.367 g). The solution was heated to 90\\u00b0 while being magnetically stirred until clear. The clear solution was cooled at approx. 2\\u00b0/hour until at room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction using Rigaku Oxford diffractometer, Mo K\\u03b1 Radiation,\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/m\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.chemmater.6b03944\",\n        \"dataset_ID\": 1917,\n        \"id\": 470,\n        \"compound_name\": \"Bis(methylammonium) silver bismuth bromide\",\n        \"formula\": \"(CH3NH3)2AgBiBr6\",\n        \"group\": \"Bis(methanaminium) tribromoargentate(I) tribromobismuthate(III), (MA)2AgBiBr6\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"*\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Properties of a Lead-Free Hybrid Double Perovskite: (CH3NH3)2AgBiBr6\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"29\",\n        \"pages_start\": \"1089\",\n        \"pages_end\": \"1094\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"CH3NH3Br (synthesized from CH3NH3 and HBr), AgBr (synthesized from AgNO3 and KBr in H2O), BiBr3, PbBr2\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"0.112 g of CH3NH3Br, 0.094 g of AgBr, and 0.2243 g of BiBr3 (2:1:1 molar ratio) were loaded in an autoclave with 0.5 mL of a HBr (48% in H2O) acid solution. Additionally, 0.011 g of CH3NH3Br and 0.036 g of PbBr2 (1:1 molar ratio) were taken. The solution was heated at 433 K for 3 days and then slowly cooled to room temperature in 3 h.\",\n        \"experimental_method\": \"UV vis absorption (diffuse reflectance)\",\n        \"experimental_description\": \"PerkinElmer Lambda 750 UV-Visible spectrometer was used to measure the optical absorption measurements on a scan range was between 350 and 1300nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acs.chemmater.6b03944\",\n        \"dataset_ID\": 1924,\n        \"id\": 470,\n        \"compound_name\": \"Bis(methylammonium) silver bismuth bromide\",\n        \"formula\": \"(CH3NH3)2AgBiBr6\",\n        \"group\": \"Bis(methanaminium) tribromoargentate(I) tribromobismuthate(III), (MA)2AgBiBr6\",\n        \"organic\": \"CNH6\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"*\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis and Properties of a Lead-Free Hybrid Double Perovskite: (CH3NH3)2AgBiBr6\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"29\",\n        \"pages_start\": \"1089\",\n        \"pages_end\": \"1094\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"CH3NH3Br (synthesized from CH3NH3 and HBr), AgBr (synthesized from AgNO3 and KBr in H2O), BiBr3, PbBr2\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"0.112 g of CH3NH3Br, 0.094 g of AgBr, and 0.2243 g of BiBr3 (2:1:1 molar ratio) were loaded in an autoclave with 0.5 mL of a HBr (48% in H2O) acid solution. Additionally, 0.011 g of CH3NH3Br and 0.036 g of PbBr2 (1:1 molar ratio) were taken. The solution was heated at 433 K for 3 days and then slowly cooled to room temperature in 3 h.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using an Oxford Gemini E Ultra diffractometer, Mo K\\u03b1 radiation (\\u03bb = 0.71073\\u00c5), equipped with an Eos CCD detector.\",\n        \"physical_property\": \"299.9\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"F m -3 m\",\n        \"extraction_method\": \"Manually extracted\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1039/C7TA04690A\",\n        \"dataset_ID\": 1925,\n        \"id\": 154,\n        \"compound_name\": \"Cesium silver indium chloride\",\n        \"formula\": \"Cs2InAgCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) trichloroindiate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"InAgCl6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Composition design, optical gap and stability investigations of lead-free halide double perovskite Cs2AgInCl6\",\n        \"journal\": \"Journal of Materials Chemistry A\",\n        \"vol\": \"29\",\n        \"pages_start\": \"15031\",\n        \"pages_end\": \"15037\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"CsCl, AgCl, InCl3, HCl\",\n        \"synthesis_product\": \"Cs2AgInCl6 microcrystals\",\n        \"synthesis_description\": \"In 0.5 ml HCl, 2.4 mmol CsCl, 1.2 mmol AgCl and 1.2 mmol InCl3 were combined and heated at 423 K for 12 h. This resulted in a white powder which was filtered and washed with ethanol and dried under reduced pressure. If the heating time is prolonged to 72 h, it is possible to obtain larger crystals.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Powder X-ray diffraction using D8 Advance diffractometer (Bruker Corporation), Cu K\\u03b1 radiation, wavelength of 1.5406 \\u00c5\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.70.205330\",\n        \"dataset_ID\": 1936,\n        \"id\": 473,\n        \"compound_name\": \"Bis(phenylethyammonium) lead iodide (Bi-doped)\",\n        \"formula\": \"(C6H5C2H4NH3)2PbI4\",\n        \"group\": \"PEA lead iodide (Bi-doped), PEA PbI (Bi-doped), Phenylethylammonium lead iodide, Bis(phenylethyammonium) tetraiodoplumbate(II) (Bi-doped)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4\",\n        \"iupac\": \"bis(1-phenyl-2-aminoethane) lead (II) tetraiodide (Bi-doped)\",\n        \"last_update\": \"2022-03-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            9\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Excitons and biexcitons bound to a positive ion in a bismuth-doped inorganic-organic layered lead iodide semiconductor\",\n        \"journal\": \"PHYSICAL REVIEW B\",\n        \"vol\": \"70\",\n        \"pages_start\": \"205330-1\",\n        \"pages_end\": \"205330-6\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"PbI2, BiI3, C6H5C2H4NH3I\",\n        \"synthesis_product\": \"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\n        \"synthesis_description\": \"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"As a detector, a charge-coupled device (CCD) camera cooled by liquid nitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.70.205330\",\n        \"dataset_ID\": 1937,\n        \"id\": 473,\n        \"compound_name\": \"Bis(phenylethyammonium) lead iodide (Bi-doped)\",\n        \"formula\": \"(C6H5C2H4NH3)2PbI4\",\n        \"group\": \"PEA lead iodide (Bi-doped), PEA PbI (Bi-doped), Phenylethylammonium lead iodide, Bis(phenylethyammonium) tetraiodoplumbate(II) (Bi-doped)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4\",\n        \"iupac\": \"bis(1-phenyl-2-aminoethane) lead (II) tetraiodide (Bi-doped)\",\n        \"last_update\": \"2022-03-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            9\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Excitons and biexcitons bound to a positive ion in a bismuth-doped inorganic-organic layered lead iodide semiconductor\",\n        \"journal\": \"PHYSICAL REVIEW B\",\n        \"vol\": \"70\",\n        \"pages_start\": \"205330-1\",\n        \"pages_end\": \"205330-6\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"PbI2, BiI3, C6H5C2H4NH3I\",\n        \"synthesis_product\": \"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\n        \"synthesis_description\": \"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"As a detector, a charge-coupled device (CCD) camera cooled by liquid nitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV. PLE spectra represent detected PL at 1.4 eV.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.70.205330\",\n        \"dataset_ID\": 1938,\n        \"id\": 473,\n        \"compound_name\": \"Bis(phenylethyammonium) lead iodide (Bi-doped)\",\n        \"formula\": \"(C6H5C2H4NH3)2PbI4\",\n        \"group\": \"PEA lead iodide (Bi-doped), PEA PbI (Bi-doped), Phenylethylammonium lead iodide, Bis(phenylethyammonium) tetraiodoplumbate(II) (Bi-doped)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4\",\n        \"iupac\": \"bis(1-phenyl-2-aminoethane) lead (II) tetraiodide (Bi-doped)\",\n        \"last_update\": \"2022-03-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            9\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Excitons and biexcitons bound to a positive ion in a bismuth-doped inorganic-organic layered lead iodide semiconductor\",\n        \"journal\": \"PHYSICAL REVIEW B\",\n        \"vol\": \"70\",\n        \"pages_start\": \"205330-1\",\n        \"pages_end\": \"205330-6\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"PbI2, BiI3, C6H5C2H4NH3I\",\n        \"synthesis_product\": \"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\n        \"synthesis_description\": \"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",\n        \"experimental_method\": \"Optical absorption measurement\",\n        \"experimental_description\": \"As a detector, a charge-coupled device (CCD) camera cooled by liquid nitrogen and equipped with a polychromator was utilized. A halogen lamp was used as a probe light for optical absorption measurements.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.70.205330\",\n        \"dataset_ID\": 1939,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Excitons and biexcitons bound to a positive ion in a bismuth-doped inorganic-organic layered lead iodide semiconductor\",\n        \"journal\": \"PHYSICAL REVIEW B\",\n        \"vol\": \"70\",\n        \"pages_start\": \"205330-1\",\n        \"pages_end\": \"205330-6\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"PbI2, BiI3, C6H5C2H4NH3I\",\n        \"synthesis_product\": \"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\n        \"synthesis_description\": \"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",\n        \"experimental_method\": \"PL-spectroscopy\",\n        \"experimental_description\": \"As a detector, a charge-coupled device (CCD) camera cooled by liquid\\r\\nnitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.70.205330\",\n        \"dataset_ID\": 1940,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Excitons and biexcitons bound to a positive ion in a bismuth-doped inorganic-organic layered lead iodide semiconductor\",\n        \"journal\": \"PHYSICAL REVIEW B\",\n        \"vol\": \"70\",\n        \"pages_start\": \"205330-1\",\n        \"pages_end\": \"205330-6\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"PbI2, BiI3, C6H5C2H4NH3I\",\n        \"synthesis_product\": \"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\n        \"synthesis_description\": \"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",\n        \"experimental_method\": \"PLE-spectroscopy\",\n        \"experimental_description\": \"As a detector, a charge-coupled device (CCD) camera cooled by liquid\\r\\nnitrogen and equipped with a polychromator was utilized. PL spectra were measured with an excitation by Xe-lamp light at 2.48 eV. PLE spectra represent detected PL at 2.35 eV.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.70.205330\",\n        \"dataset_ID\": 1941,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Excitons and biexcitons bound to a positive ion in a bismuth-doped inorganic-organic layered lead iodide semiconductor\",\n        \"journal\": \"PHYSICAL REVIEW B\",\n        \"vol\": \"70\",\n        \"pages_start\": \"205330-1\",\n        \"pages_end\": \"205330-6\",\n        \"year\": \"2004\",\n        \"synthesis_starting_materials\": \"PbI2, BiI3, C6H5C2H4NH3I\",\n        \"synthesis_product\": \"dark, red, platelike crystals, with a bismuth ratio Pb/Bi of approx. 0.3%\",\n        \"synthesis_description\": \"Under an argon atmosphere, lead iodide (PbI2), bismuth iodide (BiI3) and phenylethylammonium iodide (C6H5C2H4NH3I) were mixed at a molar ratio of 0.9:0.1:2 and heated at 333K for a duration of 30 min. As a solvent, nitromethane was added for crystallization.\",\n        \"experimental_method\": \"optical absorption measurement\",\n        \"experimental_description\": \"As a detector, a charge-coupled device (CCD) camera cooled by liquid\\r\\nnitrogen and equipped with a polychromator was utilized.  A halogen\\r\\nlamp was used as a probe light for optical absorption measurements.\",\n        \"physical_property\": \"4.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41598-019-49926-z\",\n        \"dataset_ID\": 1942,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1945\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural, Photophysical, and Electronic Properties of CH3NH3PbCl3 Single Crystals\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"9\",\n        \"pages_start\": \"13311\",\n        \"pages_end\": \"13311\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead chloride (PbCl2, 99.999%, Alfa Aesar), methylammonium hydrochloride (CH3NH3Cl, 99%, Alfa Aesar), dimethylformamide (DMF) (C3H7NO, 99.5%, Merck KGaA), and dimethyl sulfoxide (DMSO) (C2H6OS, 99.7%, Sigma-Aldrich)\",\n        \"synthesis_product\": \"MAPbCl3 single crystals of size ~2.5\\u2009mm\\u2009\\u00d7\\u20092\\u2009mm\\u2009\\u00d7\\u20091\\u2009mm\",\n        \"synthesis_description\": \"0.2228 gm of CH3NH3Cl was dissolved in a 3.3 mL DMSO: DMF (1:1) solution using an ultrasonic bath for 10 minutes under an N2 atmosphere at room temperature. In 3 mL of the prepared CH3NH3Cl/DMSO:DMF (1:1) solution, 0.8343 g PbCl2 was added. The mixture was stirred for 20 min until the solution becomes transparent. The solution was filtered using PVDF filter. The filtrate was transferred in a vial and kept in an oil bath undisturbed at 50 \\u00b0C for 6 ~8 h. After the formation of the crystals, they were dried with a nitrogen gun.\",\n        \"experimental_method\": \"Photoluminescence measurement at 300 K\",\n        \"experimental_description\": \"PL spectrum was recorded with a HORIBA iHR-550 spectrometer, liquid-nitrogen cooled CCD detector, and semiconductor laser operated at 266 nm.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Pm3m\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41598-019-49926-z\",\n        \"dataset_ID\": 1943,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural, Photophysical, and Electronic Properties of CH3NH3PbCl3 Single Crystals\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"9\",\n        \"pages_start\": \"13311\",\n        \"pages_end\": \"13311\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead chloride (PbCl2, 99.999%, Alfa Aesar), methylammonium hydrochloride (CH3NH3Cl, 99%, Alfa Aesar), dimethylformamide (DMF) (C3H7NO, 99.5%, Merck KGaA), and dimethyl sulfoxide (DMSO) (C2H6OS, 99.7%, Sigma-Aldrich)\",\n        \"synthesis_product\": \"MAPbCl3 single crystals of size ~2.5\\u2009mm\\u2009\\u00d7\\u20092\\u2009mm\\u2009\\u00d7\\u20091\\u2009mm\",\n        \"synthesis_description\": \"0.2228 gm of CH3NH3Cl was dissolved in a 3.3 mL DMSO: DMF (1:1) solution using an ultrasonic bath for 10 minutes under an N2 atmosphere at room temperature. In 3 mL of the prepared CH3NH3Cl/DMSO:DMF (1:1) solution, 0.8343 g PbCl2 was added. The mixture was stirred for 20 min until the solution becomes transparent. The solution was filtered using PVDF filter. The filtrate was transferred in a vial and kept in an oil bath undisturbed at 50 \\u00b0C for 6 ~8 h. After the formation of the crystals, they were dried with a nitrogen gun.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"The spectrum was recorded using a combination of a HOROBA iHR-550 spectrometer, Xenon lamp, and liquid-nitrogen cooled CCD detector\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41598-019-49926-z\",\n        \"dataset_ID\": 1945,\n        \"id\": 1,\n        \"compound_name\": \"Methylammonium lead chloride\",\n        \"formula\": \"CH6NPbCl3\",\n        \"group\": \"(CH3NH3)PbCl3 , (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3, Methylammonium trichloroplumbate(II)\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbCl3, Lead chloride\",\n        \"iupac\": \"methanaminium lead (II) chloride\",\n        \"last_update\": \"2022-07-29\",\n        \"description\": \"CH3NH3PbX3, (CH3NH3)PbCl3, MAPbCl3, (MA)PbCl3\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1942\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural, Photophysical, and Electronic Properties of CH3NH3PbCl3 Single Crystals\",\n        \"journal\": \"Scientific Reports\",\n        \"vol\": \"9\",\n        \"pages_start\": \"13311\",\n        \"pages_end\": \"13311\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"Lead chloride (PbCl2, 99.999%, Alfa Aesar), methylammonium hydrochloride (CH3NH3Cl, 99%, Alfa Aesar), dimethylformamide (DMF) (C3H7NO, 99.5%, Merck KGaA), and dimethyl sulfoxide (DMSO) (C2H6OS, 99.7%, Sigma-Aldrich)\",\n        \"synthesis_product\": \"MAPbCl3 single crystals of size ~2.5\\u2009mm\\u2009\\u00d7\\u20092\\u2009mm\\u2009\\u00d7\\u20091\\u2009mm\",\n        \"synthesis_description\": \"0.2228 gm of CH3NH3Cl was dissolved in a 3.3 mL DMSO: DMF (1:1) solution using an ultrasonic bath for 10 minutes under an N2 atmosphere at room temperature. In 3 mL of the prepared CH3NH3Cl/DMSO:DMF (1:1) solution, 0.8343 g PbCl2 was added. The mixture was stirred for 20 min until the solution becomes transparent. The solution was filtered using PVDF filter. The filtrate was transferred in a vial and kept in an oil bath undisturbed at 50 \\u00b0C for 6 ~8 h. After the formation of the crystals, they were dried with a nitrogen gun.\",\n        \"experimental_method\": \"Photoluminescence measurement at 300 K\",\n        \"experimental_description\": \"PL spectrum was recorded with a HORIBA iHR-550 spectrometer, liquid-nitrogen cooled CCD detector, and semiconductor laser operated at 266 nm.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Pm3m\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 1946,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"AEQT.2HBr, PbBr2, ethylene glycol, HBr (aq)\",\n        \"synthesis_product\": \"(AEQT)PbBr4 crystals\",\n        \"synthesis_description\": \"Prepare the starting AEQT.2HBr salt using a technique similar to that described in detail for the synthesis of AMQT.2HCl [1]. \\r\\n\\r\\nGrow (AEQT)PbBr4 crystals from a slowly cooled, saturated, aqueous solution containing the organic and inorganic salts. First, weigh 14.5 mg (0.025 mmol) of AEQT.2HBr and 18.3 mg (0.050 mmol) of PbBr2 and add to a test tube under an inert atmosphere. Dissolve the contents in the sealed tube at 120 \\u00b0C in a solvent mixture of 22 mL of deionized water, 1 mL of ethylene glycol, and 2 drops of 48% aqueous HBr, forming a nominally saturated yellow solution. Slow cool at 2 \\u00b0C/h to 0 \\u00b0C, to form small, yellow, sheetlike crystals of the desired (AEQT)PbBr4 compound. To prevent deforming the thin crystals, remove the product from the reaction tube using a pipet and deposit on filter paper to absorb the solution.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Photoluminescence spectrum was recorded at 290 K using a Spex Fluorolog-2 spectrofluorometer. 360 nm light from a xenon arc lamp was used as the excitation source, after being passed through a SPEX 1680 0.22 m double monochromator. The emission was passed through a similar monochromator and detected with a SPEX 1911F photomultiplier tube (PMT).\\r\\nCrystals of the material were pressed between two sapphire windows. The deposit on sapphire was then mounted on a coldfinger. The temperature was maintained using an APD Cryogenics displex system.\",\n        \"physical_property\": \"290.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 1947,\n        \"id\": 3,\n        \"compound_name\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead bromide\",\n        \"formula\": \"C20H22N2S4PbBr4\",\n        \"group\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4, 5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene tetrabromoplumbate(II)\",\n        \"organic\": \"C20H22N2S4\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"5,5\\u2018\\u2018\\u2018-bis(aminoethyl)-2,2\\u2018:5\\u2018,2\\u2018\\u2018:5\\u2018\\u2018,2\\u2018\\u2018\\u2018-quaterthiophene lead(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"AE4TPbBr4, (AEQT)PbBr4, AEQTPbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Design, Structure, and Optical Properties of Organic-Inorganic Perovskites Containing an Oligothiophene Chromophore\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"38\",\n        \"pages_start\": \"6246\",\n        \"pages_end\": \"6256\",\n        \"year\": \"1999\",\n        \"synthesis_starting_materials\": \"(AEQT)PbBr4, quartz, acetone, ethanol\",\n        \"synthesis_product\": \"(AEQT)PbBr4 thin film. Film thickness between 500 \\u00c5 and 900 \\u00c5.\",\n        \"synthesis_description\": \"To prepare (AEQT)PbBr4, sonicate quartz samples in 2% (w/v) detergent solution in water (20 min), then sonicate in acetone (20 min) and ethanol (20 min). Boil in ethanol (5 min) and place in a 130 \\u00b0C oven to dry. Add 0.003 g of (AEQT)PbBr4 compounds to 0.1 mL of methanol, and sonicate again for 10 min. Place the charge dropwise via a syringe on the tantalum heater of the SSTA chamber. Close chamber and evacuate all solvent with a rotary mechanical pump. Switch on a turbomolecular pump, and pump system to approximately 10^{-7} Torr. To initiate the evaporation, pass a large current of approximately 65 A through the heater for about 4 s. Anneal the (AEQT)PbBr4 films at 180 \\u00b0C for 15 min.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Photoluminescence spectrum was recorded at room temperature using a Spex Fluorolog-2 spectrofluorometer. 370 nm light from a xenon arc lamp was used as the excitation source, after being passed through a SPEX 1680 0.22 m double monochromator. The emission was passed through a similar monochromator and detected with a SPEX 1911F photomultiplier tube (PMT).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.7b01094\",\n        \"dataset_ID\": 1948,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead(II) Halide-Based Hybrid Perovskites Templated by Acene Alkylamines: Crystal Structures, Optical Properties, and Piezoelectricity\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"9291\",\n        \"pages_end\": \"9302\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(PMA)2PbBr4 crystals, DMF, glass substrates\",\n        \"synthesis_product\": \"Thin film on glass\",\n        \"synthesis_description\": \"Dissolve the 2D single crystals into DMF at a concentration 6%\\u223c10% relative to the total weight. Spin-coat at 3000 rpm for 30 s on glass substrates. Anneal in air at 100 \\u00b0C for 10 min before measurement.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Optical absorption spectra were obtained using a Shimadzu UV-3600 spectrophotometer.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Cmc2(1)\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 1949,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            950\n        ],\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Diffuse reflectance spectra\",\n        \"experimental_description\": \"Diffuse reflectance spectra were measured in a Shimadzu UV 2450 instrument. A Ba2SO4 powder palette was the reference used. The reflectance was converted to absorbance.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 1950,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            951\n        ],\n        \"primary_name\": \"photoluminescence peak position\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, butylammonium iodide\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, butyric acid, toluene, and butylamine were mixed in a capped flask. Separately, butylammonium iodide was dissolved in toluene with butylamine and butyric acid. The two solutions were combined and stirred until an insoluble yellow solid precipitated. The solid was removed by centrifuging at 6000 rpm for 3 minutes. The yellow solid was redispersed in toluene and centrifuged a second time, to produce the final products.  \\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Photoluminescence spectra\",\n        \"experimental_description\": \"A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the powder films to measure photoluminescence spectra. Excitation was perpendicular to the sample and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.9b03439\",\n        \"dataset_ID\": 1953,\n        \"id\": 249,\n        \"compound_name\": \"Bis(benzylammonium) formmamidinium lead iodide\",\n        \"formula\": \"(C6H5CH2NH3)2[CH(NH2)2PbI3]PbI4\",\n        \"group\": \"(BZA)2[FAPbI3]PbI4, (BZA)2(FA)Pb2I7, bis(benzylaminium) diaminomethanide tetraiodoplumbate(II)\",\n        \"organic\": \"C7H10N, CH5N2\",\n        \"inorganic\": \"Lead iodide\",\n        \"iupac\": \"bis(benzylaminium) diaminomethanide lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"n=2\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthesis of Polycrystalline Ruddlesden\\u2013Popper Organic Lead Halides and Their Growth Dynamics\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"9472\",\n        \"pages_end\": \"9479\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, toluene, butyric acid, butylamine, formamidinium acetate\",\n        \"synthesis_product\": \"Powder film on glass substrate\",\n        \"synthesis_description\": \"PbI2, toluene, butyric acid, and butylamine were mixed in a capped flask. Separately, formamidinium acetate was dissolved in toluene and butyric acid. For this n=2 layered perovskite, the suspension was heated to 70 degrees Celsius and then cooled slowly, and the color changed from dark brown to red. The bright red is characteristic of this system. Centrifugation at 6000 rpm for three minutes was used to first isolate the solid, which was then re-dispersed in hexane and centrifuged again. This obtained the final paintlike paste solid. \\r\\nThe paintlike paste was then deposited on a glass substrate. A Pasteur pipette was used to spread the paste over the surface and was then allowed to dry.\",\n        \"experimental_method\": \"Photoluminescence Spectra\",\n        \"experimental_description\": \"A Horiba-Jobin Yvon Fluorolog-3 instrument was used on the films to measure photoluminescence spectra. Excitation was perpendicular to the film and emission was collected at an angle of ~15 degrees. The data was corrected according to the lamp and detector details by using algorithms from the equipment software.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b04064\",\n        \"dataset_ID\": 1956,\n        \"id\": 386,\n        \"compound_name\": \"piperidiniumethylammonium lead iodide\",\n        \"formula\": \"C14H34I8N4Pb2\",\n        \"group\": \"(PipEA)[PbI4]\",\n        \"organic\": \"C7H20N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-ethanaminium)-1H-piperidin-1-ium\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Improved Photovoltaic Efficiency and Amplified Photocurrent Generation in Mesoporous n = 1 Two-Dimensional Lead\\u2212Iodide Perovskite Solar Cells\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"31\",\n        \"pages_start\": \"890\",\n        \"pages_end\": \"898\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N/A\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"Thin films were prepared by dissolving (PipEA)[PbI4] (0.50M) in DMF and was spin-coated onto glass substrates at 3000 rpm for 30 s. The films were then heated to 130\\u00baC for 10 minutes.\",\n        \"experimental_method\": \"steady-state PL spectroscopy\",\n        \"experimental_description\": \"Excitation at 405 nm. Data was collected with a Horiba Fluoromax-3 spectrometer with a 0.5nm wavelength resolution.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P121/n1\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ee43822h\",\n        \"dataset_ID\": 1957,\n        \"id\": 38,\n        \"compound_name\": \"Cesium lead iodide\",\n        \"formula\": \"CsPbI3\",\n        \"group\": \"cesium lead iodide, cesium triiodoplumbate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            516,\n            517,\n            518,\n            519,\n            520,\n            521,\n            522\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            367\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formamidinium lead trihalide: a broadly tunable perovskite for efficient planar heterojunction solar cells\",\n        \"journal\": \"Energy & Environmental Science\",\n        \"vol\": \"7\",\n        \"pages_start\": \"982\",\n        \"pages_end\": \"988\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"CsI, PbI2, dimethyl sulfoxide\",\n        \"synthesis_product\": \"CsPbI3 film\",\n        \"synthesis_description\": \"Equimolar amounts of CsI and PbI2 were dissolved in dimethyl sulfoxide at 0.6M, in a nitrogen-filled glovebox. Films were spin-coated at 2000rpm and annealed at 100 degrees C for 5 minutes in the glovebox.\",\n        \"experimental_method\": \"Optical absorption\",\n        \"experimental_description\": \"Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ee43822h\",\n        \"dataset_ID\": 1958,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            137\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formamidinium lead trihalide: a broadly tunable perovskite for efficient planar heterojunction solar cells\",\n        \"journal\": \"Energy & Environmental Science\",\n        \"vol\": \"7\",\n        \"pages_start\": \"982\",\n        \"pages_end\": \"988\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"Methylamine (CH3NH2), (HI) 57 wt % in water, PbI2\",\n        \"synthesis_product\": \"MAPbI3 film\",\n        \"synthesis_description\": \"React ~24 mL methylamine (CH3NH2) solution 33 wt% in absolute ethanol with ~10 mL hydroiodic acid (HI) 57 wt % in water with excess methylamine under nitrogen atmosphere in ~100 mL ethanol at room temperature. Crystallize methylammonium iodide (CH3NH3I) using a rotary evaporator to form a white colored powder. Prepare MAPbI3 precursor by dissolving equimolar amounts of methylammonium iodide and PbI2 in DMF at 0.88M in a nitrogen-filled glovebox. Spin-coat film at 2000rpm and anneal at 100 \\u00b0C for 5 minutes in the glovebox.\",\n        \"experimental_method\": \"Optical absorption\",\n        \"experimental_description\": \"Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c3ee43822h\",\n        \"dataset_ID\": 1959,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            368\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formamidinium lead trihalide: a broadly tunable perovskite for efficient planar heterojunction solar cells\",\n        \"journal\": \"Energy & Environmental Science\",\n        \"vol\": \"7\",\n        \"pages_start\": \"982\",\n        \"pages_end\": \"988\",\n        \"year\": \"2014\",\n        \"synthesis_starting_materials\": \"FAI, PbI2, N,N-dimethylformamide (DMF)\",\n        \"synthesis_product\": \"FAPbI3 film\",\n        \"synthesis_description\": \"FAI and PbI2 were dissolved in anhydrous DMF in a 1:1 molar ratio, at 0.88M. 60\\u00b5l of hydroiodic acid (57%w/w) was added to 1ml of the solution. The FAPbI3 precursor was diluted down to 0.55M with DMF. The precursor solution was spin-coated and annealed on glass in a nitrogen-filled glovebox at 170\\u00b0C for 25 minutes.\",\n        \"experimental_method\": \"optical absorption\",\n        \"experimental_description\": \"Transmittance and reflectance spectra were collected with a Varian Cary 300 UV-Vis spectrophotometer with an internally coupled integrating sphere.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual entry\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1961,\n        \"id\": 476,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide : Iodine-intercalated\",\n        \"formula\": \"C8H24N2PbI4:I2\",\n        \"group\": \"(C4H9NH3)2PbI4:I2, (C4H12N)2PbI4:I2, BA2PbI4:I2, (BA)2PbI4:I2, I2-intercalated bis(butane-1-aminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"I2-intercalated bis(butane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-04-18\",\n        \"description\": \"Molecular I2 doped (BA)2PbI4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            17\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I, I2\",\n        \"synthesis_product\": \"(BA)2PbI4:I2\",\n        \"synthesis_description\": \"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether. Dried (BA)2PbI4 crystals were placed in an open plastic tube which was kept in a closed glass vial containing molecular I2 for 2-3 hours at room temperature.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using Kubelka-Munk transformation: (\\u03b1/S = (1 \\u2212 R)^2/2R); \\u03b1 is the absorption coefficient, and S is the scattering coefficient R is the reflectance.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1962,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I\",\n        \"synthesis_product\": \"(BA)2PbI4\",\n        \"synthesis_description\": \"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether.\",\n        \"experimental_method\": \"UV-visible absorption\",\n        \"experimental_description\": \"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using the Kubelka-Munk transformation; (\\u03b1/S = (1 \\u2212 R)^2/2R); \\u03b1 is the absorption coefficient, S is the scattering coefficient, and R is the reflectance.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1965,\n        \"id\": 476,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide : Iodine-intercalated\",\n        \"formula\": \"C8H24N2PbI4:I2\",\n        \"group\": \"(C4H9NH3)2PbI4:I2, (C4H12N)2PbI4:I2, BA2PbI4:I2, (BA)2PbI4:I2, I2-intercalated bis(butane-1-aminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"I2-intercalated bis(butane-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2022-04-18\",\n        \"description\": \"Molecular I2 doped (BA)2PbI4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            17\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I, I2\",\n        \"synthesis_product\": \"(BA)2PbI4:I2\",\n        \"synthesis_description\": \"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether. Dried (BA)2PbI4 crystals were placed in an open plastic tube which was kept in a closed glass vial containing molecular I2 for 2-3 hours at room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Recorded on FLS 980 (Edinburgh Instruments).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1967,\n        \"id\": 17,\n        \"compound_name\": \"Bis(Butylammonium) lead iodide\",\n        \"formula\": \"C8H24N2PbI4\",\n        \"group\": \"bis(butane-1-aminium) tetraiodoplumbate(II), (C4H9NH3)2PbI4, (C4H12N)2PbI4, BA2PbI4, (BA)2PbI4\",\n        \"organic\": \"C4H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            476\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"lead oxide (10 mmol),  hydriodic acid (10 mL), hypophosphorous acid (1.7 mL ),  C4H9NH3I\",\n        \"synthesis_product\": \"(BA)2PbI4\",\n        \"synthesis_description\": \"Single crystals of (BA)2PbI4 were synthesized in a method called acid precipitation. Through constant stirring and heating, lead oxide (10 mmol) was dissolved in a solution that contained hydriodic acid (10 mL) and hypophosphorous acid (1.7 mL). After, C4H9NH3I was added to the mixture, causing the bright yellow solution to change to an orange color precipitate. Continuous heating of the mixture followed until the precipitate was fully dissolved, forming orange crystals at room temperature. The crystals were obtained via filtration and bathed in diethyl ether.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Recorded on FLS 980 (Edinburgh Instruments).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1968,\n        \"id\": 477,\n        \"compound_name\": \"Hexaflourobenzene bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4:C6F6\",\n        \"group\": \"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H12N, C6F6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"hexafluorobenzene bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            179\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%), hexafluorobenzene (HFB, Sigma Aldrich, 99%)\",\n        \"synthesis_product\": \"(PEA)2SnI4 : HFB crystals\",\n        \"synthesis_description\": \"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 \\u02daC under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration. 50 mg of these crystals was dissolved in a mixture of 2 mL methanol and 2 mL HFB. The obtained dark yellow solution was kept open in a glove box. As the solvent evaporates (PEA)2SnI4:HFB crystals precipitate out. The crystals were filtered, dried and stored in a glove box for further use.\",\n        \"experimental_method\": \"UV-visible absorption\",\n        \"experimental_description\": \"Optical diffuse-reflectance spectra were collected at room temperature using a Shimadzu UV-3600 plus UV-VIS-NIR spectrophotometer. The reflectance spectra were converted to absorbance by using the Kubelka-Munk transformation; (\\u03b1/S = (1 \\u2212 R)^2/2R); \\u03b1 is the absorption coefficient, S is the scattering coefficient, and R is the reflectance.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1970,\n        \"id\": 477,\n        \"compound_name\": \"Hexaflourobenzene bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4:C6F6\",\n        \"group\": \"(PEA)2SnI4:HFB, (C6H5CH2CH2NH3)2(SnI4):HFB, hexafluorobenzene intercalated bis(phenylethanaminium) tetraiodostannate(II)\",\n        \"organic\": \"C8H12N, C6F6\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"hexafluorobenzene bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            179\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%), hexafluorobenzene (HFB, Sigma Aldrich, 99%)\",\n        \"synthesis_product\": \"(PEA)2SnI4 : HFB crystals\",\n        \"synthesis_description\": \"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 \\u02daC under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration. 50 mg of these crystals was dissolved in a mixture of 2 mL methanol and 2 mL HFB. The obtained dark yellow solution was kept open in a glove box. As the solvent evaporates (PEA)2SnI4:HFB crystals precipitate out. The crystals were filtered, dried and stored in a glove box for further use.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Recorded on FLS 980 (Edinburgh Instruments).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.202003509\",\n        \"dataset_ID\": 1971,\n        \"id\": 179,\n        \"compound_name\": \"Bis(phenethylammonium) tin iodide\",\n        \"formula\": \"C16H24N2SnI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodostannate(II), (PEA)2SnI4, (C6H5CH2CH2NH3)2(SnI4)\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"SnI4, Tin iodide\",\n        \"iupac\": \"bis(phenylethanaminium) tin iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            477\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Molecular Intercalation and Electronic Two Dimensionality in Layered Hybrid Perovskites\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"11653\",\n        \"pages_end\": \"11659\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Tin(II) oxide (Sigma Aldrich, 97%), hydriodic acid (Sigma Aldrich, 57% w/w in H2O, 99.9%),  hypophosphorous acid (Avra, 50% w/w H2O),  phenylethylamine (Sigma Aldrich, 99.9%)\",\n        \"synthesis_product\": \"(PEA)2SnI4 crystals\",\n        \"synthesis_description\": \"Single crystals of (PEA)2SNI4 were synthesized by adding tin (II) oxide (0.6 mmol), hydriodic acid ( 5 mL), and hypophosphorous acid (3 mL) into a sealed vial and heated at 90 \\u02daC under constant stirring. After tin (II) oxide dissolved in the solution and yielded a dark yellow color, phenethylamine (1.2 mmol) was injected into the sealed vial by a syringe. A brown sheet of crystals of (PEA)2SNI4 produced after the solution was cooled to room temperature. The crystals were then obtained via filtration and were stored in an N2 glove box.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Recorded on FLS 980 (Edinburgh Instruments).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.5b04231\",\n        \"dataset_ID\": 1972,\n        \"id\": 46,\n        \"compound_name\": \"Cesium silver bismuth chloride\",\n        \"formula\": \"Cs2AgBiCl6\",\n        \"group\": \"Dicesium trichloroargentate(I) \\u00b5-dichloro trichlorobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"Cs2AgBiCl6, Cesium silver(I) bismuth(III) chloride\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            2\n        ],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Cs2AgBiX6 (X = Br, Cl): New Visible Light Absorbing, Lead-Free Halide Perovskite Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"1348\",\n        \"pages_end\": \"1354\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cs2CO3 (99+%, Strem Chemicals), HCl (Sigma-Aldrich, 37%), AgNO3 (99.9+%, Alfa Aesar), NaCl (ACS Reagent, GFS Chemicals), BiCl3 (\\u226598%, Aldrich)\",\n        \"synthesis_product\": \"Polycrystalline Cs2AgBiCl6\",\n        \"synthesis_description\": \"Cs2CO3 was reacted with HCl to prepare CsCl. The solution was evaporated, and the resulting solids were filtered and washed with ethanol. AgCl was precipitated by mixing aqueous solutions of AgNO3 and NaCl. \\r\\nThen, 8 mL of 12.1 M HCl and 2 mL of a 50% solution of H3PO2 were mixed and heated to 120 \\u00b0C. To it, 1.89 mmol of AgCl and an equal amount of BiCl3 were added. When dissolved, 3.78 mmol of CsCl was added. The precipitate was collected [possibly after cooling down the solution to room temperature] on filter paper, washed with ethanol, and dried overnight.\",\n        \"experimental_method\": \"X-ray Powder Diffraction\",\n        \"experimental_description\": \"Powder XRD data were collected on a Bruker D8 powder diffractometer (40 kV, 50 mA, sealed Cu X-ray tube) equipped with an incident beam Ge 111 monochromator and Lynx Eye position-sensitive detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"F m -3 m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.5b04231\",\n        \"dataset_ID\": 1973,\n        \"id\": 223,\n        \"compound_name\": \"Cesium silver bismuth bromide\",\n        \"formula\": \"Cs2AgBiBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"bulk polycrystalline\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Cs2AgBiX6 (X = Br, Cl): New Visible Light Absorbing, Lead-Free Halide Perovskite Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"1348\",\n        \"pages_end\": \"1354\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cs2CO3 (99+%, Strem Chemicals), HBr (Fluka, \\u226548%), AgNO3 (99.9+%, Alfa Aesar), KBr (99+%, Alfa Aesar), Bi2O3 (\\u226599.0%, J.T. Baker)\",\n        \"synthesis_product\": \"Polycrystalline Cs2AgBiCl6\",\n        \"synthesis_description\": \"Cs2CO3 was reacted with HBr to prepare CsBr. The solution was evaporated, and the resulting solids were filtered and washed with ethanol. AgBr was precipitated by mixing aqueous solutions of AgNO3 and KBr. BiBr3 was prepared by reacting Bi2O3 with HBr. The mixture was heated until fully dissolved, evaporated to dryness, and then filtered and washed with ethanol. \\r\\nThen, 8 mL of 8.84 M HBr and 2 mL of a 50% solution of H3PO2 were mixed and heated to 120 \\u00b0C. To it, 1.41 mmol of AgBr and an equal amount of BiBr3 were added. When dissolved, 2.82 mmol of CsBr was added. The precipitate was collected [possibly after cooling down the solution to room temperature] on filter paper, washed with ethanol, and dried overnight.\",\n        \"experimental_method\": \"X-ray Powder Diffraction\",\n        \"experimental_description\": \"Powder XRD data were collected on a Bruker D8 powder diffractometer (40 kV, 50 mA, sealed Cu X-ray tube) equipped with an incident beam Ge 111 monochromator and Lynx Eye position-sensitive detector.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"Fm-3m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.5b13294\",\n        \"dataset_ID\": 1974,\n        \"id\": 223,\n        \"compound_name\": \"Cesium silver bismuth bromide\",\n        \"formula\": \"Cs2AgBiBr6\",\n        \"group\": \"Dicesium tribromoargentate(I) tribromobismuthate(III)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"AgBiBr6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A Bismuth-Halide Double Perovskite with Long Carrier Recombination Lifetime for Photovoltaic Applications\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"2138\",\n        \"pages_end\": \"2141\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Solid CsBr, BiBr, 9-M HBr, Solid AgBr\",\n        \"synthesis_product\": \"orange powder\",\n        \"synthesis_description\": \"First, solid CsBr (0.426 g, 2.00 mmol) and BiBr (0.449 g, 1.00 mmol) were dissolved in 10 mL of 9-M HBr. Afterward, solid AgBr (0.188 g, 1.00 mmol) was added to the mixture. The vial was then capped, heated to 110\\u00ba C for 2 hours, and cooled to room temperature. As a result, an orange-powder precipitate formed and was filtered on a glass frit and dried under low pressure overnight.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"Low-temperature photoluminescence was measured using a spectrograph (Acton Research SpectraPro 500i) equipped with a silicon CCD array detector (Hamamatsu). Samples were cooled to liquid helium temperatures using a Janus ST-500 cold-finger cryostat.\",\n        \"physical_property\": \"22.6\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge Digitizer\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1975,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            480,\n            1977\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1976,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            477\n        ],\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1977,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            480,\n            1975\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\",\n        \"physical_property\": \"77.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1978,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            481,\n            1979\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\",\n        \"physical_property\": \"77.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1979,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            481,\n            1978\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether.In an N2-filled glove box,  SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1980,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            478\n        ],\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box,  SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1984,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"An Oxford-Diffraction Xcalibur-2 CCD diffractometer with graphite-monochromated Mo K\\u03b1 radiation was used to collect the single crystal XRD data.\",\n        \"physical_property\": \"120.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1985,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            479\n        ],\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence excitation\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PLE spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1986,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            482,\n            1987\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1987,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            482,\n            1986\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"FLS980 spectrofluorometer (Edinburgh Instruments) was used to record the PL spectra. liquid nitrogen was used to cool the samples.\",\n        \"physical_property\": \"77.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1990,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence quantum efficiency using integrating sphere\",\n        \"experimental_description\": \"An integrating sphere incorporated in FLS980 spectrofluorometer (Edinburgh Instruments) was used to measure the PLQE.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1991,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence quantum efficiency using integrating sphere\",\n        \"experimental_description\": \"An integrating sphere incorporated in FLS980 spectrofluorometer (Edinburgh Instruments) was used to measure the PLQE.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1992,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence quantum efficiency using integrating sphere\",\n        \"experimental_description\": \"An integrating sphere incorporated in FLS980 spectrofluorometer (Edinburgh Instruments) was used to measure the PLQE.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1993,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1994\n        ],\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 \\u00b0C/ min\\u0002, under a nitrogen flux of 100 mL/min\\u0002.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1994,\n        \"id\": 57,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium bromide) tin bromide\",\n        \"formula\": \"C16H56N8Br4SnBr6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-bromide) hexabromostannate(II), (C4N2H14Br)4SnBr6, (C4H14N2Br)4SnBr6\",\n        \"organic\": \"C4H14N2Br\",\n        \"inorganic\": \"SnBr6, Tin bromide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-bromide) tin(II) bromide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1993\n        ],\n        \"primary_name\": \"Degradation onset temperature\",\n        \"primary_unit\": \"\\u00b0C\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"dimethylformamide (DMF, 99.8%), Tin(II) bromide (SnBr2), N,N0-dimethylethylenediamine (99%), hydrobromic acid (48 wt% in H2O), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium bromide was prepared by adding HBr solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, Tin(ii) bromide and N,N\\u2032-dimethylethylene-1,2-diammonium bromide were mixed in a 1\\u2006:\\u20064 molar ratio in DMF to form a clear precursor solution. DCM was diffused into this DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 \\u00b0C/ min\\u0002, under a nitrogen flux of 100 mL/min\\u0002.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1995,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1997\n        ],\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 \\u00b0C/ min\\u0002, under a nitrogen flux of 100 mL/min\\u0002.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1997,\n        \"id\": 58,\n        \"compound_name\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diammonium iodide) tin iodide\",\n        \"formula\": \"C16H56N8I4SnI6\",\n        \"group\": \"tetra(N,N'-dimethylethylene-1,2-diaminium-iodide) hexaiodostannate(II), (C4N2H14I)4SnI6, (C4H14N2I)4SnI6\",\n        \"organic\": \"C4H14N2I\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"tetra(N,N\\u2032-dimethylethylene-1,2-diaminium-iodide) tin(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1995\n        ],\n        \"primary_name\": \"Degradation onset temperature\",\n        \"primary_unit\": \"\\u00b0C\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\\u03b3-butyrolactone (GBL, 99%), tin(II) iodide (SnI2), N,N\\u2032-dimethylethylenediamine, hydriodic acid (55%), Dichloromethane (DCM, 99.9%)\",\n        \"synthesis_product\": \"Red crystals\",\n        \"synthesis_description\": \"N,N\\u2032-dimethylethylene-1,2-diammonium iodide was prepared by adding HI solution (2.2 equiv.) into N,N\\u2032-dimethylethylenediamine (1 equiv.) in ethanol at 0 \\u00b0C. The solvent was then removed under vacuum, and the resulting solid was washed with ethyl ether. In an N2-filled glove box, SnI2 and N,N\\u2032-dimethylethylene-1,2-diammonium iodide were mixed in a 1\\u2006:\\u20064 molar ratio in GBL to form a clear precursor solution. DCM was diffused into this GBL solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 \\u00b0C/ min, under a nitrogen flux of 100 mL/min.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1998,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1999\n        ],\n        \"primary_name\": \"Thermogravimetric behavior\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"\\u00b0C\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 \\u00b0C/ min, under a nitrogen flux of 100 mL/min.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/C7SC04539E\",\n        \"dataset_ID\": 1999,\n        \"id\": 59,\n        \"compound_name\": \"Bis(1-butyl-1-methylpyrrolidinium) antimony chloride\",\n        \"formula\": \"C18H40N2SbCl5\",\n        \"group\": \"bis(1-butyl-1-methylpyrrolidinium) pentachloroantimonate(III), (C9NH20)2SbCl5, (C9H20N)2SbCl5\",\n        \"organic\": \"C9H20N\",\n        \"inorganic\": \"SbCl5, Antimony chloride\",\n        \"iupac\": \"bis(1-butyl-1-methylpyrrolidinium) antimony(III) chloride\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            1998\n        ],\n        \"primary_name\": \"Degradation onset temperature\",\n        \"primary_unit\": \"\\u00b0C\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Luminescent zero-dimensional organic metal halide hybrids with near-unity quantum efficiency\",\n        \"journal\": \"Chemical Science\",\n        \"vol\": \"9\",\n        \"pages_start\": \"586\",\n        \"pages_end\": \"593\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"antimony trichloride (SbCl3), dimethylformamide (DMF, 99.8%), 1-butyl-1-methylpyrrolidinium chloride (C9NH20Cl)\",\n        \"synthesis_product\": \"Colorless crystals\",\n        \"synthesis_description\": \"Antimony(II) chloride and 1-butyl-1-methylpyrrolidinium chloride were mixed in a 1 : 2 molar ratio in DMF. Bulk crystals were prepared by diffusing acetone into DMF solution at room temperature overnight. The obtained crystals were washed with acetone and dried under reduced pressure.\",\n        \"experimental_method\": \"Thermogravimetric analysis (TGA)\",\n        \"experimental_description\": \"TA instruments Q50 TGA system was used to collect the data. The sample was heated at a rate of 5 \\u00b0C/ min, under a nitrogen flux of 100 mL/min.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.8b00542\",\n        \"dataset_ID\": 2001,\n        \"id\": 266,\n        \"compound_name\": \"3-(aminomethyl)piperidinium methylammonium lead iodide\",\n        \"formula\": \"(C6H16N2)(CH3NH3)Pb2I7\",\n        \"group\": \"(3-AMP)(MA)Pb2I7, (3AMP)(MA)Pb2I7, 3-(methanaminium)piperidinium methanaminium septaiodo diplumbate(II)\",\n        \"organic\": \"C6H16N2, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"3-(methanaminium)piperidinium methanaminium lead iodide\",\n        \"last_update\": \"2021-11-09\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Dion\\u2212Jacobson 2D Lead Iodide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"140 (10)\",\n        \"pages_start\": \"3775\",\n        \"pages_end\": \"3783\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"3-(aminomethyl)piperidine (3AMP), Methylammonium iodide (MAI, >99.5%), Lead oxide (PbO, 99.9%), hydroiodic acid (HI, 57 wt % in H2O, distilled, stabilized, 99.95%), hypophosphorous acid solution (H3PO2, 50 wt % in water)\",\n        \"synthesis_product\": \"Dark red crystals\",\n        \"synthesis_description\": \"669 mg (3 mmol) PbO powder was dissolved in 6 mL hydroiodic acid and 1 mL hypophosphorous acid solution by heating under stirring for 5\\u221210 min at \\u223c130 \\u00b0C until the solution turned clear bright yellow. 318 mg (2 mmol) MAI was added to this solution under heating. In a separate vial, 0.5 mL HI was added to 57 mg (0.5 mmol) 3AMP under stirring. The protonated 3AMP solution was added into the previous solution under heating and stirring for 5 min. The crystals precipitate during slow cooling to room temperature.\",\n        \"experimental_method\": \"Diffuse Reflectance Spectra\",\n        \"experimental_description\": \"A Shimadzu UV-3600 UV-vis NIR spectrometer operating at 200-1000 nm was used for optical diffuse reflectance measurements. BaSO4 was used as the 100% reflectance reference. The reflectance was converted to absorption using Kubelka\\u2212Munk equation: \\u03b1/S = (1 \\u2212 R)^2/(2R), where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively. Band gap was estimated from the absorption plot (possibly the step-like feature at energy higher than the excitonic resonance peak).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Engauge digitizer\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b01025\",\n        \"dataset_ID\": 2003,\n        \"id\": 79,\n        \"compound_name\": \"Formamidinium germanium iodide\",\n        \"formula\": \"HC(NH2)2GeI3\",\n        \"group\": \"diaminomethanide triiodogermanate(II), FAGeI3, HC(NH2)2GeI3, (NH2)2CHGeI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"GeI3, Germanium iodide\",\n        \"iupac\": \"diaminomethanide germanium iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Germanium Iodide Perovskite Semiconductors: Active Lone Pairs, Structural Distortions, Direct and Indirect Energy Gaps, and Strong Nonlinear Optical Properties\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"137\",\n        \"pages_start\": \"6804\",\n        \"pages_end\": \"6819\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), formamidinium chloride (HC(NH2)2Cl, 98%)\",\n        \"synthesis_product\": \"orange, elongated hexagonal tubular CH3C(NH2)2GeI3 crystals\",\n        \"synthesis_description\": \"GeI4 was synthesized from GeO2 and HI, and HC(NH2)2I was synthesized by reacting ethanolic solutions of HC(NH)(NH2) (prepared by neutralizing HC(NH2)2Cl with sodium methoxide in EtOH and discarding NaCl) with aqueous HI.\\r\\nFor the synthesis of HC(NH2)2GeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, HC(NH2)2I (172 mg, 1 mmol) was dissolved. The solution was evaporated to approximately half its original volume by heating at 120 \\u00b0C. The stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements.  BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1 - R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.5b01025\",\n        \"dataset_ID\": 2004,\n        \"id\": 480,\n        \"compound_name\": \"Cesium Germanium Iodide\",\n        \"formula\": \"CsGeI3\",\n        \"group\": \"*\",\n        \"organic\": \"none\",\n        \"inorganic\": \"CsGeI3\",\n        \"iupac\": \"-\",\n        \"last_update\": \"2022-05-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band gap (optical, diffuse reflectance)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Hybrid Germanium Iodide Perovskite Semiconductors: Active Lone Pairs, Structural Distortions, Direct and Indirect Energy Gaps, and Strong Nonlinear Optical Properties\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"137\",\n        \"pages_start\": \"6804\",\n        \"pages_end\": \"6819\",\n        \"year\": \"2015\",\n        \"synthesis_starting_materials\": \"hydroiodic acid (HI, 57% in water), hypophosphorous acid (H3PO2, 50% in water), GeO2 (99.999%), CsI (99.95%)\",\n        \"synthesis_product\": \"Black truncated octahedral CsGeI3 crystals\",\n        \"synthesis_description\": \"GeI4 was synthesized from GeO2 and HI.\\r\\nFor the synthesis of CsGeI3, aqueous HI (6.8 mL, 7.58 M) and aqueous H3PO2 (3.4 mL, 9.14 M) were taken in a 2-neck flask. The mixture was degassed by passing a stream of nitrogen through it for 1 min. The following procedure was performed under N2. GeI4 (580 mg, 1 mmol) was dissolved in the mixture upon heating the flask to 120 \\u00b0C using an oil bath, under constant magnetic stirring, forming a bright yellow solution. To it, CsI (260 mg, 1 mmol) was dissolved. After 5 minutes, the stirring was discontinued, and the solution was left to cool down to room temperature. Upon cooling, the crystals formed, and they were allowed to grow for 24 h. Then, the crystals were taken out from the N2 environment and were filtered, and washed with a minimum amount of degassed EtOH.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"A Shimadzu UV-3101 PC double-beam, double-monochromator spectrophotometer operating from 200 to 2500 nm was used to collect optical diffuse reflectance measurements.  BaSO4 was used as a non-absorbing reflectance reference. The band gap was then estimated by converting reflectance to absorbance via the Kubelka-Munk equation: \\u03b1/S = (1 - R)^2/2R, where R is the reflectance and \\u03b1 and S are the absorption and scattering coefficients, respectively.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R3m\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-019-08980-x\",\n        \"dataset_ID\": 2006,\n        \"id\": 82,\n        \"compound_name\": \"3-fluorophenethylammonium lead iodide\",\n        \"formula\": \"C16H22N2F2PbI4\",\n        \"group\": \"3-fluorophenethanaminium tetraiodoplumbate(II), mF1PEA2PbI4\",\n        \"organic\": \"C8H11NF\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"3-fluorophenethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthetic control over orientational degeneracy of spacer cations enhances solar cell efficiency in two-dimensional perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1276\",\n        \"pages_end\": \"1276\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2 (99.9985%, from Alfa Aesar), HI, 3-fluorophenethylammonium iodide (synthesized)\",\n        \"synthesis_product\": \"Orange crystals\",\n        \"synthesis_description\": \"26.4\\u2009mg PbI2 and 30.7 mg 3-fluorophenethylammonium iodide were dissolved in 1 ml 57\\u2009wt% stabilized HI at 90\\u00b0C. The solution was slowly cooled down to room temperature at a rate of 1\\u00b0C/h and the solids were collected.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\",\n        \"physical_property\": \"300.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"C2/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-019-08980-x\",\n        \"dataset_ID\": 2007,\n        \"id\": 83,\n        \"compound_name\": \"2-fluorophenethylammonium lead iodide\",\n        \"formula\": \"C16H22N2F2PbI4\",\n        \"group\": \"2-fluorophenethanaminium tetraiodoplumbate(II), oF1PEA2PbI4\",\n        \"organic\": \"C8H11NF\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"2-fluorophenethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthetic control over orientational degeneracy of spacer cations enhances solar cell efficiency in two-dimensional perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1276\",\n        \"pages_end\": \"1276\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2 (99.9985%, from Alfa Aesar), HI, 2-fluorophenethylammonium iodide (synthesized)\",\n        \"synthesis_product\": \"Orange-yellow crystals\",\n        \"synthesis_description\": \"26.4\\u2009mg PbI2 and 30.7 mg 2-fluorophenethylammonium iodide were dissolved in 1 ml 57\\u2009wt% stabilized HI at 90\\u00b0C. The solution was slowly cooled down to room temperature at a rate of 1\\u00b0C/h and the solids were collected.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker D8 Quest ECO diffractometer equipped with a microfocus  Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\",\n        \"physical_property\": \"300.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/s41467-019-08980-x\",\n        \"dataset_ID\": 2008,\n        \"id\": 80,\n        \"compound_name\": \"4-fluorophenethylammonium lead iodide\",\n        \"formula\": \"C16H22N2F2PbI4\",\n        \"group\": \"4-fluorophenethanaminium tetraiodoplumbate(II), pF1PEA2PbI4\",\n        \"organic\": \"C8H11NF\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"4-fluorophenethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Synthetic control over orientational degeneracy of spacer cations enhances solar cell efficiency in two-dimensional perovskites\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"10\",\n        \"pages_start\": \"1276\",\n        \"pages_end\": \"1276\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2 (99.9985%, from Alfa Aesar), 4-fluorophenethylammonium iodide (synthesized), HI\",\n        \"synthesis_product\": \"Orange rectangular crystal\",\n        \"synthesis_description\": \"26.4\\u2009mg PbI2 and 30.7 mg 4-fluorophenethylammonium iodide were dissolved in 1.5 ml 57\\u2009wt% stabilized HI at 90\\u00b0C. The solution was slowly cooled down to room temperature at a rate of 1\\u00b0C/h and the solids were collected.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Bruker D8 Quest ECO diffractometer equipped with a microfocus Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) source and Photon 50 CMOS half-plate detector was used for SCXRD data collection at room temperature.\",\n        \"physical_property\": \"300.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1038/ncomms14051\",\n        \"dataset_ID\": 2009,\n        \"id\": 102,\n        \"compound_name\": \"N, N\\u2032-dimethylethylenediamine lead bromide\",\n        \"formula\": \"C4H14N2PbBr4\",\n        \"group\": \"N, N\\u201a\\u00c4\\u2264-dimethylethylenediaminium tetrabromoplumbate(II), C4N2H14PbBr4\",\n        \"organic\": \"C4H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"N, N\\u2032-dimethylethylenediaminium lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"One-dimensional organic lead halide perovskites with efficient bluish white-light emission\",\n        \"journal\": \"Nature Communications\",\n        \"vol\": \"8\",\n        \"pages_start\": \"145051\",\n        \"pages_end\": \"145051\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Lead (II) bromide (PbBr2, 99.999%), N, N'-dimethylethylenediamine (99%), hydrobromic acid (HBr, 48 wt.% in H2O)\",\n        \"synthesis_product\": \"Colorless needle-like C4N2H14PbBr4 crystals\",\n        \"synthesis_description\": \"In 10\\u2009ml HBr, PbBr2 (0.100 g, 0.27 mmol) and N, N' -dimethylethylenediamine (0.024 g, 0.27 mmol) were dissolved by sonication for 10 minutes. 1 mL of this solution was kept in a vapor diffusion chamber. Acetone was diffused into this solution for 24 h.\",\n        \"experimental_method\": \"single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The data were collected on a Bruker SMART APEX II diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"103.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Imma\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/acs.inorgchem.7b02285\",\n        \"dataset_ID\": 2010,\n        \"id\": 107,\n        \"compound_name\": \"N,N-dimethylphenylene-p-diammonium lead iodide\",\n        \"formula\": \"C8H14N2PbI4\",\n        \"group\": \"benzene-1,4-di(methanaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C8H14N2\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"benzene-1,4-di(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead Halide Perovskites Templated by a Conjugated Asymmetric Diammonium\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"14991\",\n        \"pages_end\": \"14998\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Pb(CH3COO)2\\u00b73H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HI (57 wt % in H2O, stabilized with H3PO4, 99.95%), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",\n        \"synthesis_product\": \"Red block-like crystal\",\n        \"synthesis_description\": \"Pb(CH3COO)2\\u00b73H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HI and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at \\u221270 \\u00b0C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 \\u00d7 10 mL). The precipitate was redissolved in 5 mL of HI and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"a Bruker Quazar SMART APEXII diffractometer with Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation was used to collect the data.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/acs.inorgchem.7b02285\",\n        \"dataset_ID\": 2011,\n        \"id\": 108,\n        \"compound_name\": \"N,N-dimethylphenylene-p-diammonium lead bromide\",\n        \"formula\": \"C8H14N2PbBr4\",\n        \"group\": \"benzene-1,4-di(methanaminium) tetrabromoplumbate(II)\",\n        \"organic\": \"C8H14N2\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"benzene-1,4-di(methanaminium) lead (II) bromide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Lead Halide Perovskites Templated by a Conjugated Asymmetric Diammonium\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"14991\",\n        \"pages_end\": \"14998\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"Pb(CH3COO)2\\u00b73H2O (99.999% trace metals basis), N,N-dimethylene-p-diamine (97%), HBr (48 wt % in H2O), H3PO4 (85 wt % in H2O), ethanol (99.9%), and diethyl ether (99%)\",\n        \"synthesis_product\": \"Yellow block-like crystal\",\n        \"synthesis_description\": \"Pb(CH3COO)2\\u00b73H2O (2.2 g, 6.8 mmol) was dissolved in 9 ml HBr and 1 ml H3PO4 under heating. 0.92g N,N-Dimethylene-p-diamine (920 mg, 6.8 mmol) was dissolved in 5 mL ethanol and the previous acid solution was added dropwise over 10 min at \\u221270 \\u00b0C while stirring. The mixture was sonicated at room temperature for 5 minutes to produce the solids. The obtained powder was filtered and washed with diethyl ether (5 \\u00d7 10 mL). The precipitate was redissolved in 5 mL of HBr and 1 mL of H3PO4 and half of the solution was evaporated by heating. The solution was allowed to cool. The obtained crystals were washed with diethyl ether.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"a Bruker Quazar SMART APEXII diffractometer with Mo K\\u03b1 (\\u03bb = 0.71073 \\u00c5) radiation was used to collect the data.\",\n        \"physical_property\": \"100.0 (\\u00b12.0)\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/n\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 2012,\n        \"id\": 110,\n        \"compound_name\": \"bis(2-phenethylammonium) methylammonium lead iodide\",\n        \"formula\": \"C17H30N3Pb2I7\",\n        \"group\": \"bis(2-phenylethanaminium) methanaminium septaiodo diplumbate(II), (C6H5(CH2)2NH3)2(CH3NH3)Pb2I7, (PEA)2(MA)Pb2I7\",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb2I7, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) methanaminium lead (II) iodide\",\n        \"last_update\": \"2022-06-02\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            604\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",\n        \"synthesis_product\": \"Red (PEA)2MAPb2I7 crystals\",\n        \"synthesis_description\": \"6 mmol PbO, 18 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 \\u00b0C. The vial was then kept in an oven at 110 \\u00b0C for 4 h. The solution was then slowly cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"For steady-state PL measurements, the details are not available in the paper.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 2013,\n        \"id\": 126,\n        \"compound_name\": \"bis(phenylethylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C18H36N4Pb3I10\",\n        \"group\": \"(C6H5(CH2)2NH3)2(CH3NH3)2Pb3I10, (PEA)2(MA)2Pb3I10, bis(2-phenylethanaminium) bismethanaminium decaiodo triplumbate(II) \",\n        \"organic\": \"C8H12N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethanaminium) bismethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Hydroiodic acid (HI, 57% w/w in water, Alpha Aesar), Lead oxide (PbO, 99%, Sigma-Aldrich), Methylammonium Iodide (MAI, >99%, Dyesol), Phenylethylamine (PEA)\",\n        \"synthesis_product\": \"Black (PEA)2MA2Pb3I10 crystals\",\n        \"synthesis_description\": \"10 mmol PbO, 24 mmol MAI, and 1 mmol PEA are dissolved in HI in a 20 mL vial at 90 \\u00b0C. The vial was then kept in an oven at 110 \\u00b0C for 4 h. The solution was then slowly cooled to room temperature.\",\n        \"experimental_method\": \"Photoluminescence\",\n        \"experimental_description\": \"For steady-state PL measurements, the details are not available in the paper.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.201806452\",\n        \"dataset_ID\": 2014,\n        \"id\": 118,\n        \"compound_name\": \"Cesium tin iodide (0D)\",\n        \"formula\": \"Cs4SnI6\",\n        \"group\": \"tetracesium hexaiodostannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI6, Tin iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Emissive Self-Trapped Excitons in Fully Inorganic Zero- Dimensional Tin Halides\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"57\",\n        \"pages_start\": \"11329\",\n        \"pages_end\": \"11333\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"Cesium bromide (CsBr, 99%), tin (II) iodide (SnI2, 99%)\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"Mix CsBr and SnI2 in a 4.5:1 molar ratio, mortar, and press together into a pellet (> 5 tons of pressure, 12 mm die). Seal pellet under vacuum (10-2 \\u2013 10-3 mbar) in a Pyrex tube and heat to 350 \\u00b0C for 60 hours. Open tube in the glovebox, and repeat the process until the formation of single crystals.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"XtraLAB Synergy, Dualflex, Pilatus 300K diffractometer. PhotonJet (Cu) X-ray source (CuK\\u03b1, \\u03bb=1.54184 \\u00c5; micro-focus sealed X-ray tube) and mirror monochromator. Data processed and refined with CrysAlis PRO 1.171.39.31d (Rigaku OD, 2017), SHELXS, XL, and Olex2.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"trigonal\",\n        \"label\": \"\",\n        \"space_group\": \"R-3c\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 2016,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"hydriodic acid (57% w/w in water, Alpha Aesar), phenethylamine (PEA),  lead oxide (PbO, 99%, Sigma-Aldrich)\",\n        \"synthesis_product\": \"Orange (PEA)2PbI4 crystals\",\n        \"synthesis_description\": \"In 30 mL HI solution, PEA, and PbO (ratio: 1.72: 3.45 mmol) were dissolved. The solution was heated at 110\\u00ba C for 4 hours and subsequently cooled to room temperature. Once the solution cooled, single crystals formed.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.8b03436\",\n        \"dataset_ID\": 2017,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"unknown\",\n        \"representative\": false,\n        \"code\": \"VESTA\",\n        \"level_of_theory\": \"DFT\",\n        \"xc_functional\": \"PBE+SOC+vdW\",\n        \"k_point_grid\": \"6x6x1\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"PAW\",\n        \"numerical_accuracy\": \"Plane-wave cutoff energy: 500 eV\",\n        \"title\": \"Layer-Dependent Rashba Band Splitting in 2D Hybrid Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"30\",\n        \"pages_start\": \"8538\",\n        \"pages_end\": \"8545\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.6b03207\",\n        \"dataset_ID\": 2018,\n        \"id\": 157,\n        \"compound_name\": \"Cesium tin iodide\",\n        \"formula\": \"Cs2SnI6\",\n        \"group\": \"Dicesium hexastannate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"SnI6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-06-23\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect Tolerance to Intolerance in the Vacancy-Ordered Double Perovskite Semiconductors Cs2SnI6 and Cs2TeI6\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"8453\",\n        \"pages_end\": \"8464\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), SnI4\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"In a beaker, slowly add \\u223c0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve SnI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the SnI4 precursors gently to T \\u2248 60 \\u00b0C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the SnI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 \\u00b0C for 24 h.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Data were collected at the 11-BM-B beamline at the Advanced Photon Source, Argonne National Laboratory.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.6b03207\",\n        \"dataset_ID\": 2019,\n        \"id\": 158,\n        \"compound_name\": \"Cesium tellurium iodide\",\n        \"formula\": \"Cs2TeI6\",\n        \"group\": \"Dicesium hexatellurate(II), Cs2TeI6\",\n        \"organic\": \"None\",\n        \"inorganic\": \"TeI6\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-01\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Defect Tolerance to Intolerance in the Vacancy-Ordered Double Perovskite Semiconductors Cs2SnI6 and Cs2TeI6\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"138\",\n        \"pages_start\": \"8453\",\n        \"pages_end\": \"8464\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Cesium carbonate (Cs2CO3), Hydroiodic acid HI (aqueous, 57%), hypophosphorous acid (H3PO2), TeI4\",\n        \"synthesis_product\": \"Black crystals\",\n        \"synthesis_description\": \"In a beaker, slowly add \\u223c0.5 mmol of Cs2CO3 to 3 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2) and stir to dissolve. In a separate beaker, dissolve TeI4 in 15 mL of absolute ethanol and 2 mL of 57% hydriodic acid (aqueous, 1.5% H3PO2), to which excess elemental iodine was added. Heat the beaker containing the TeI4 precursors gently to T \\u2248 60 \\u00b0C to encourage solubility. Once the solids had completely dissolved into their respective solutions, quickly add the Cs2CO3/HI solution to the TeI4 solution, resulting in a black precipitate. Stir reaction for an additional 30 min. Collect the precipitate by centrifugation and wash three times with absolute ethanol. Dry the final products at 60 \\u00b0C for 24 h.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"Data were collected at the 11-BM-B beamline at the Advanced Photon Source, Argonne National Laboratory.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manual entry\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7cc02408h\",\n        \"dataset_ID\": 2020,\n        \"id\": 180,\n        \"compound_name\": \"Bis(phenethylammonium) cadmium iodide\",\n        \"formula\": \"C16H24N2CdI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CdI4, Cadmium iodide\",\n        \"iupac\": \"bis(phenylethanaminium) cadmium iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A near-room-temperature organic\\u2013inorganic hybrid ferroelectric: [C6H5CH2CH2NH3]2[CdI4]\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"5764\",\n        \"pages_end\": \"5766\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",\n        \"synthesis_product\": \"Colorless block-like crystals\",\n        \"synthesis_description\": \"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2\\u2010phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Frames were collected using RAXIS IP diffractometer with Mo\\u2010K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"220.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c9dt00945k\",\n        \"dataset_ID\": 2021,\n        \"id\": 181,\n        \"compound_name\": \"N,N-dimethylethanolammonium cadmium chloride\",\n        \"formula\": \"C4H12NOCdCl3\",\n        \"group\": \"N,N-dimethylethanolaminium trichlorocadmate(II), (DMEA)CdCl3, (C4H12NO)CdCl3\",\n        \"organic\": \"C4H12NO\",\n        \"inorganic\": \"CdCl3, Cadmium chloride\",\n        \"iupac\": \"N,N-dimethylethanolaminium cadmium chloride\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ultra high phase transition temperature in a metal-halide perovskite-type material containing unprecedented hydrogen bonding interactions\",\n        \"journal\": \"Dalton Transactions\",\n        \"vol\": \"48\",\n        \"pages_start\": \"6621\",\n        \"pages_end\": \"6626\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"N,N-dimethylethanolamine (DMEA), CdCl2 and HCl (37% concentrated)\",\n        \"synthesis_product\": \"colorless strip (DMEA)CdCl3 crystals\",\n        \"synthesis_description\": \"A solution mixture of DMEA (10 mmol), CdCl2 (10 mmol), and HCl (20 mmol) was slowly evaporated at room temperature for two weeks.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using Rigaku CCD diffractometer with Mo-K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5)\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc00786a\",\n        \"dataset_ID\": 2022,\n        \"id\": 183,\n        \"compound_name\": \"N-methyldabconium lead iodide\",\n        \"formula\": \"C7H15N2PbI3\",\n        \"group\": \"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",\n        \"organic\": \"C7H15N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N-methyldabconium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Extra thermo- and water-stable one-dimensional organic\\u2013inorganic hybrid perovskite [N-methyldabconium]PbI3 showing switchable dielectric behaviour, conductivity and bright yellow-green emission\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4321\",\n        \"pages_end\": \"4324\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"[N-methyldabconium]I, PbI2 and DMF\",\n        \"synthesis_product\": \"Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals\",\n        \"synthesis_description\": \"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using graphite-monochromated Mo Ka (\\u03bb = 0.71073 \\u00c5) radiation on a CCD area detector (Bruker SMART)\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Pbca\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c8cc00786a\",\n        \"dataset_ID\": 2023,\n        \"id\": 183,\n        \"compound_name\": \"N-methyldabconium lead iodide\",\n        \"formula\": \"C7H15N2PbI3\",\n        \"group\": \"N-methyldabconium trichloroplumbate(II), (N-methyldabconium)PbI3\",\n        \"organic\": \"C7H15N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N-methyldabconium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"nm\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Extra thermo- and water-stable one-dimensional organic\\u2013inorganic hybrid perovskite [N-methyldabconium]PbI3 showing switchable dielectric behaviour, conductivity and bright yellow-green emission\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"54\",\n        \"pages_start\": \"4321\",\n        \"pages_end\": \"4324\",\n        \"year\": \"2018\",\n        \"synthesis_starting_materials\": \"[N-methyldabconium]I, PbI2 and DMF\",\n        \"synthesis_product\": \"Light-yellow rod-shaped [N-methyldabconium]PbI3 crystals\",\n        \"synthesis_description\": \"A 1:1 molar ratio of PbI2 and [N-methyldabconium]I was mixed in DMF, where crystals were obtained after a slow evaporation at 333K after 2 weeks.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were recorded using graphite-monochromated Mo Ka (\\u03bb = 0.71073 \\u00c5) radiation on a CCD area detector (Bruker SMART)\",\n        \"physical_property\": \"373.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P 6(3)/m m c\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b03095\",\n        \"dataset_ID\": 2024,\n        \"id\": 184,\n        \"compound_name\": \"Dimethylammonium lead iodide\",\n        \"formula\": \"C2H8NPbI3\",\n        \"group\": \"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N-dimethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectric Properties, and Ionic Transport in the [(CH3)2NH2]PbI3 Organic\\u2013Inorganic Hybrid with 2H-Hexagonal Perovskite Structure\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"4918\",\n        \"pages_end\": \"4927\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(CH3)2NH solution (40 wt % in H2O), HI solution (57 wt % in H2O), PbI2 (99%)\",\n        \"synthesis_product\": \"yellow needle-shaped [(CH3)2NH2]PbI3 crystals\",\n        \"synthesis_description\": \"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 were then mixed and ground for 15 min. The obtained yellow powder was dissolved in THF, and the solvent was allowed to evaporate at room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using a Bruker Kappa diffractometer equipped with an APEX II CCD detector using monochromatic Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"hexagonal\",\n        \"label\": \"\",\n        \"space_group\": \"P 6(3)/m m c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.inorgchem.6b03095\",\n        \"dataset_ID\": 2025,\n        \"id\": 184,\n        \"compound_name\": \"Dimethylammonium lead iodide\",\n        \"formula\": \"C2H8NPbI3\",\n        \"group\": \"N,N-dimethanaminium triiodoplumbate(II), DMAPbI3, (CH3)2NH2PbI3\",\n        \"organic\": \"C2H8N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"N,N-dimethanaminium lead (II) iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Phase Transition, Dielectric Properties, and Ionic Transport in the [(CH3)2NH2]PbI3 Organic\\u2013Inorganic Hybrid with 2H-Hexagonal Perovskite Structure\",\n        \"journal\": \"Inorganic Chemistry\",\n        \"vol\": \"56\",\n        \"pages_start\": \"4918\",\n        \"pages_end\": \"4927\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"(CH3)2NH solution (40 wt % in H2O), HI solution (57 wt % in H2O), PbI2 (99%)\",\n        \"synthesis_product\": \"yellow needle-shaped [(CH3)2NH2]PbI3 crystals\",\n        \"synthesis_description\": \"Initially [(CH3)2NH2]I was synthesized by mixing (CH3)2NH solution with HI in an ice bath, where the product was achieved after using a rotary evaporator. Equimolar amounts of this and PbI2 were then mixed and ground for 15 min. The obtained yellow powder was dissolved in THF, and the solvent was allowed to evaporate at room temperature.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected using a Bruker Kappa diffractometer equipped with an APEX II CCD detector using monochromatic Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5).\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P 2(1)/c\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.0c00101\",\n        \"dataset_ID\": 2026,\n        \"id\": 285,\n        \"compound_name\": \"(3AMPY)0.5(4AMPY)0.5Sn2I6\",\n        \"formula\": \"C6H10I6N2Sn2\",\n        \"group\": \"3-(methanaminium)pyridinium 4-(methanaminium)pyridinium hexaiodo distannate(II)\",\n        \"organic\": \"C6H16N2\",\n        \"inorganic\": \"Sn2I6, Tin iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium 4-(methanaminium)pyridinium tin iodide\",\n        \"last_update\": \"2022-07-06\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"2\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Three-dimensional Lead Iodide Perovskitoid Hybrids with High X-ray Photoresponse\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"142\",\n        \"pages_start\": \"6625\",\n        \"pages_end\": \"6637\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"SnCl2\\u20222H2O (99%), hydroiodic acid (57 wt % in H2O, 99.95%), hypophosphorous acid solution (50 wt % in H2O), 3-(aminomethyl)-pyridine (99%), and 4-(aminomethyl)pyridine (98%)\",\n        \"synthesis_product\": \"black plate-like crystals\",\n        \"synthesis_description\": \"SnCl2\\u20222H2O (2 mmol 451.3 mg) was dissolved in 2.5 mL of HI, and the solution was heated and constantly stirred. Once a yellow solution was obtained, 3AMPY (0.25 mmol, 50.8 \\u03bcL) and 4AMPY (0.25 mmol) were added to hypophosphorous acid (0.5 mL) in a separate vial. Both solutions were combined, heated at 240\\u00ba C, and stirred for 5 minutes. The temperature was then lowered to 125\\u00ba C until black crystals precipitated. Crystals were obtained via suction filtration.\",\n        \"experimental_method\": \"Single crystal X-ray diffraction (XRD)\",\n        \"experimental_description\": \"SC-XRD were executed with a STOE IPDS II or IPDS 2T diffractometer with Mo K\\u03b1 radiation (\\u03bb=0.71073 \\u00c5) at 50 kV and 40 mA. Corrections were performed with X-AREA, X-RED, and XSHAPE programs\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"Im\",\n        \"extraction_method\": \"Manually extracted from a publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 2029,\n        \"id\": 60,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"C12H32N2PbI4\",\n        \"group\": \"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"hexylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"C6H16N, HI, PbI2, EtO2\",\n        \"synthesis_product\": \"Powder of (C6H13NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence spectra\",\n        \"experimental_description\": \"Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 2031,\n        \"id\": 61,\n        \"compound_name\": \"Bis(dodecylammonium) lead iodide\",\n        \"formula\": \"C24H56N2PbI4\",\n        \"group\": \"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",\n        \"organic\": \"C12H28N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(dodecyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"dodecylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HI, DA (C12H25NH3), Et2O, PbI2\",\n        \"synthesis_product\": \"Thin film of (C12H25NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 \\u00b0C.\",\n        \"experimental_method\": \"Photoluminescence spectra\",\n        \"experimental_description\": \"Steady-state photoluminescence emission spectra of spin-coated films on glass were measured at room temperature with a step size of 1 nm in an Edinburgh Instruments FLS980 fluorimeter by exciting with monochromated light with a 2 nm bandwidth at 480 nm.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 2032,\n        \"id\": 60,\n        \"compound_name\": \"Bis(hexylammonium) lead iodide\",\n        \"formula\": \"C12H32N2PbI4\",\n        \"group\": \"bis(hexyl-1-aminium) tetraiodoplumbate(II), HA2PbI4, (C6H13NH3)2PbI4, (C6H16N)2PbI4\",\n        \"organic\": \"C6H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(hexyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"hexylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"C6H16N, HI, PbI2, EtO2\",\n        \"synthesis_product\": \"Thin film of (C12H25NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare hexylammonium iodide salts via neutralization of HI with HA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving HAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 \\u00b0C.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Steady-state room-temperature absorption spectra were determined by placing spin-coated films on glass in a using an HP 8453 spectrometer.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.7b10223\",\n        \"dataset_ID\": 2033,\n        \"id\": 61,\n        \"compound_name\": \"Bis(dodecylammonium) lead iodide\",\n        \"formula\": \"C24H56N2PbI4\",\n        \"group\": \"bis(dodecyl-1-aminium) tetraiodoplumbate(II), DA2PbI4, (C12H25NH3)2PbI4, (C12H28N)2PbI4\",\n        \"organic\": \"C12H28N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(dodecyl-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-11\",\n        \"description\": \"dodecylammonium lead iodide\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Formation of Long-Lived Color Centers for Broadband Visible Light Emission in Low-Dimensional Layered Perovskites\",\n        \"journal\": \"JOURNAL OF THE AMERICAN CHEMICAL SOCIETY\",\n        \"vol\": \"139\",\n        \"pages_start\": \"18632\",\n        \"pages_end\": \"18639\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"HI, DA (C12H25NH3), Et2O, PbI2\",\n        \"synthesis_product\": \"Thin film of (C12H25NH3)2PbI4\",\n        \"synthesis_description\": \"Prepare dodecylammonium iodide salts via neutralization of HI with DA. Remove unreacted species by evaporation. Purify product by recrystallization in minimal diethyl ether/excess hexane and isolate via vacuum filtration. Prepare films by spin-coating or drop-casting solutions (prepared by dissolving DAI and PbI2 powders at a 2.5:1 molar ratio in a 1:0.34 volume ratio mixture of THF and methanol). Spin-coat films from solutions of 20 mg/mL at 2000 rpm for 30 s and anneal for 15 min at 70 \\u00b0C.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"Steady-state room-temperature absorption spectra were determined by placing spin-coated films on glass in a using an HP 8453 spectrometer.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2034,\n        \"id\": 484,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a room temperature (298K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction (SC-XRD)\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON\\u2019s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Differential scanning calorimetry\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2035,\n        \"id\": 484,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a room temperature (298K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction (SC-XRD)\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON\\u2019s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2036,\n        \"id\": 484,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a room temperature (298K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction (SC-XRD)\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON\\u2019s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2037,\n        \"id\": 487,\n        \"compound_name\": \"S-2-methylbutylammonium lead bromide\",\n        \"formula\": \"C10H28N2PbBr4\",\n        \"group\": \"(S-2-MeBA)2PbBr4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbBr4, lead bromide\",\n        \"iupac\": \"S-2-methylbutylammonium lead (II) Bromide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a low temperature (100K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbBr2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbBr4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbBr2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbBr4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbBr4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbBr4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"Differential scanning calorimetry (DSC)\",\n        \"experimental_description\": \"A TA Discovery DSC 2500 was used to carry out low-temperature conventional differential scanning calorimetry (DSC) measurements. The instrument was under helium purge with a 5 K/min ramp from 298 K to 124 K and back to 298 K (with use of an LN2P cooler). Sample powder was loaded into a Tzero Hermetic aluminum pan, with temperature and enthalpy calibrated in advance.\\r\\n\\r\\nA similar instrument was used to perform high-temperature DSC measurements under nitrogen purge. The ramp rate was 5 K/min from 298 K to 603 K. An aluminum pan was hermetically sealed to contain samples.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 2043,\n        \"id\": 208,\n        \"compound_name\": \"3-(aminomethyl)pyridinium lead iodide\",\n        \"formula\": \"C6H10N2PbI4\",\n        \"group\": \"(3AMPY)PbI4, (C6H10N2)PbI4, 3-(methanaminium)pyridinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, 3-(aminomethyl)pyridine (3AMPY), Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Red plate-like (3AMPY)PbI4 crystal\",\n        \"synthesis_description\": \"To a hot yellow solution of 0.5 mmol PbO in 2.5 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.5 mmol 3AMPY neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-like crystals precipitate upon cooling the above to 120\\u00b0C and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.9b06398\",\n        \"dataset_ID\": 2046,\n        \"id\": 208,\n        \"compound_name\": \"3-(aminomethyl)pyridinium lead iodide\",\n        \"formula\": \"C6H10N2PbI4\",\n        \"group\": \"(3AMPY)PbI4, (C6H10N2)PbI4, 3-(methanaminium)pyridinium tetraiodoplumbate(II)\",\n        \"organic\": \"C6H10N2\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"3-(methanaminium)pyridinium lead (II) iodide\",\n        \"last_update\": \"2022-02-10\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Two-Dimensional Dion \\u2212 Jacobson Hybrid Lead Iodide Perovskites with Aromatic Diammonium Cations\",\n        \"journal\": \"J. Am. Chem. Soc.\",\n        \"vol\": \"141\",\n        \"pages_start\": \"12880\",\n        \"pages_end\": \"12890\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbO, 3-(aminomethyl)pyridine (3AMPY), Aq. HI, Aq. H3PO2\",\n        \"synthesis_product\": \"Red plate-like (3AMPY)PbI4 crystal\",\n        \"synthesis_description\": \"To a hot yellow solution of 0.5 mmol PbO in 2.5 ml Aq. HI at 240\\u00b0C (hot-plate temperature), a solution of 0.5 mmol 3AMPY neutralized in 0.5 ml concentrated Aq. H3PO2 was added under stirring. Red plate-like crystals precipitate upon cooling the above to 120\\u00b0C and further down to 80\\u00b0C within 1 hr.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"The frames were collected using an STOE IPDS II or IPDS 2T diffractometer Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and operating at 50 kV and 40 mA.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c04213\",\n        \"dataset_ID\": 2072,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of Annealing and Composition on the Crystal Structure of Mixed-Halide, Ruddlesden\\u2013Popper Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"3109\",\n        \"pages_end\": \"3122\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"phenethylammonium iodide (C8H12IN), lead iodide (PbI2)\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"(PEA)I, amd PbI2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196\\u00b0C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 \\u03bcm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm \\u00d7 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 \\u00b0C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 \\u00d7 10\\u20135 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110\\u00b0.\",\n        \"experimental_method\": \"UV-vis absorption\",\n        \"experimental_description\": \"UV\\u2212vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"as-grown\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually extracted\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c04213\",\n        \"dataset_ID\": 2073,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of Annealing and Composition on the Crystal Structure of Mixed-Halide, Ruddlesden\\u2013Popper Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"3109\",\n        \"pages_end\": \"3122\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"phenethylammonium iodide (C8H12IN), lead iodide (PbI2)\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"(PEA)I, amd PbI2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196\\u00b0C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 \\u03bcm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm \\u00d7 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 \\u00b0C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 \\u00d7 10\\u20135 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110\\u00b0.\",\n        \"experimental_method\": \"UV-vis photoluminescence\",\n        \"experimental_description\": \"PL spectroscopy measurements were taken using a HORIBA Jobin Yvon LabRam ARAMIS system. All films were excited using a 325 HeCd laser source with a 1% filter. Samples were kept in ambient air conditions.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"as-grown\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually extracted\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c04213\",\n        \"dataset_ID\": 2074,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of Annealing and Composition on the Crystal Structure of Mixed-Halide, Ruddlesden\\u2013Popper Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"3109\",\n        \"pages_end\": \"3122\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"phenethylammonium bromide (C8H12BrN), lead bromide (PbBr2)\",\n        \"synthesis_product\": \"Thin film of (C12H25NH3)2PbBr4\",\n        \"synthesis_description\": \"(PEA)Br and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196\\u00b0C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 \\u03bcm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm \\u00d7 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 \\u00b0C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 \\u00d7 10\\u20135 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110\\u00b0.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"UV\\u2212vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"as-grown\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c04213\",\n        \"dataset_ID\": 2075,\n        \"id\": 11,\n        \"compound_name\": \"Bis(phenylethylammonium) lead bromide\",\n        \"formula\": \"C16H24N2PbBr4\",\n        \"group\": \"bis(2-phenylethan-1-aminium) tetrabromoplumbate(II), (PEA)2PbBr4, (C6H5C2H4NH3)2PbBr4, (C8H12N)2PbBr4, PEA lead bromide, (PEA) lead bromide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(2-phenylethan-1-aminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of Annealing and Composition on the Crystal Structure of Mixed-Halide, Ruddlesden\\u2013Popper Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"3109\",\n        \"pages_end\": \"3122\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"phenethylammonium bromide (C8H12BrN), lead bromide (PbBr2)\",\n        \"synthesis_product\": \"Thin film of (C12H25NH3)2PbBr4\",\n        \"synthesis_description\": \"(PEA)Br and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196\\u00b0C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 \\u03bcm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm \\u00d7 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 \\u00b0C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 \\u00d7 10\\u20135 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110\\u00b0.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"PL spectroscopy measurements were taken using a HORIBA Jobin Yvon LabRam ARAMIS system. All films were excited using a 325 HeCd laser source with a 1% filter. Samples were kept in ambient air conditions.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"as-grown\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c04213\",\n        \"dataset_ID\": 2087,\n        \"id\": 488,\n        \"compound_name\": \"Bis(phenethylammonium) lead iodide(1-x) bromide(x): x = 0.25\",\n        \"formula\": \"PEA2Pb(I(1-x)Br(x))4 with x = 0.25\",\n        \"group\": \"PEA2 lead iodide bromide, PEAPbIBr, PEA2PbIBr\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"Pb(I(1-x)Br(x))4\",\n        \"iupac\": \"bis(phenethylaminium) lead (II) iodide bromide\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            9,\n            11\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of Annealing and Composition on the Crystal Structure of Mixed-Halide, Ruddlesden\\u2013Popper Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"3109\",\n        \"pages_end\": \"3122\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"phenethylammonium iodide (C8H12IN), phenethylammonium bromide (C8H12BrN), lead iodide (PbI2), lead bromide (PbBr2)\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"(PEA)I, (PEA)Br, PbI2, and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196\\u00b0C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 \\u03bcm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm \\u00d7 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 \\u00b0C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 \\u00d7 10\\u20135 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110\\u00b0.\",\n        \"experimental_method\": \"UV\\u2212vis Absorption\",\n        \"experimental_description\": \"UV\\u2212vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"as-grown\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually extracted\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c04213\",\n        \"dataset_ID\": 2088,\n        \"id\": 490,\n        \"compound_name\": \"Bis(phenethylammonium) lead iodide(1-x) bromide(x): x = 0.5\",\n        \"formula\": \"PEA2Pb(I(1-x)Br(x))4 with x = 0.5\",\n        \"group\": \"PEA2 lead iodide bromide, PEAPbIBr, PEA2PbIBr\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"Pb(I0.5Br0.5)4\",\n        \"iupac\": \"bis(phenethylaminium) lead (II) iodide bromide\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of Annealing and Composition on the Crystal Structure of Mixed-Halide, Ruddlesden\\u2013Popper Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"3109\",\n        \"pages_end\": \"3122\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"phenethylammonium iodide (C8H12IN), phenethylammonium bromide (C8H12BrN), lead iodide (PbI2), lead bromide (PbBr2)\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"(PEA)I, (PEA)Br, PbI2, and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196\\u00b0C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 \\u03bcm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm \\u00d7 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 \\u00b0C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 \\u00d7 10\\u20135 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110\\u00b0.\",\n        \"experimental_method\": \"UV\\u2212vis absorption\",\n        \"experimental_description\": \"UV\\u2212vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"as-grown\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually extracted\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c04213\",\n        \"dataset_ID\": 2089,\n        \"id\": 491,\n        \"compound_name\": \"Bis(phenethylammonium) lead iodide(1-x) bromide(x): x = 0.75\",\n        \"formula\": \"PEA2Pb(I(1-x)Br(x))4 with x = 0.75\",\n        \"group\": \"PEA2 lead iodide bromide, PEAPbIBr, PEA2PbIBr\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"Pb(I0.25Br0.75)4\",\n        \"iupac\": \"bis(phenethylaminium) lead (II) iodide bromide\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Influence of Annealing and Composition on the Crystal Structure of Mixed-Halide, Ruddlesden\\u2013Popper Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"3109\",\n        \"pages_end\": \"3122\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"phenethylammonium iodide (C8H12IN), phenethylammonium bromide (C8H12BrN), lead iodide (PbI2), lead bromide (PbBr2)\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"(PEA)I, (PEA)Br, PbI2, and PbBr2 made up the target solution in 1:1 DMSO/MEG by volume. They were mechanically mixed until visibly dissolved in solvent, taking about 5 min. In a growth chamber, the solution is cooled to -196\\u00b0C under vacuum. When frozen, the top layer is removed using an Er:YAG laser (2.94 \\u03bcm). The laser rasters across the surface to sublimate the MEG, causing the precursor material to be ejected onto the substrate (2 cm \\u00d7 2 cm of SiO2 glass) spinning 7 cm above. The substrate temperature is approximately 10 \\u00b0C while in the growth chamber. Deposit time was 4 h. Samples remained in a load lock under turbo vacuum (2 \\u00d7 10\\u20135 Torr) for an hour afterwards. The annealed films were additionally annealed for 10 min on a hot plate in an N2 environment at 110\\u00b0.\",\n        \"experimental_method\": \"UV\\u2212vis absorption\",\n        \"experimental_description\": \"UV\\u2212vis absorption spectra were acquired using a Shimadzu UV-3600 spectrophotometer. Samples of films on glass substrates were measured. Samples were kept in ambient air conditions.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"as grown\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2092,\n        \"id\": 485,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide (placeholder 485)\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium Lead Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"100 K LT phase, slow-cooling.\",\n        \"message\": \"This is a placeholder. The datasets for this material (https://materials.hybrid3.duke.edu/materials/485) can be found <a href=\\\"https://materials.hybrid3.duke.edu/materials/484\\\"> here</a>. This entry also contains data regarding other relevant structures of the material.\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction (SC-XRD)\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON\\u2019s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2093,\n        \"id\": 486,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide (placeholder 486)\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"\",\n        \"message\": \"This is a placeholder. The datasets for this material (https://materials.hybrid3.duke.edu/materials/486) can be found <a href=\\\"https://materials.hybrid3.duke.edu/materials/484\\\"> here</a>. This entry also contains data regarding other relevant structures of the material.\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction (SC-XRD)\",\n        \"experimental_description\": \"A Rigaku XtaLAB Synergy-S diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5) and functioning at 50 kV and 30 mA gathered data on (S-2-MeBA)2PbI4 crystals at room temperature (298 K). Data was also collected at 100 K, incorporating an 800 Series Cryostream Cooler. CrysAlisPro performed peak hunting, data reduction, and numerical absorption correction. SHELXS direct methods and SHELXL least-squares method solved crystal structures. PLATON\\u2019s ADDSYM tool analyzed the symmetry of full and isolated inorganic structures (default tolerance values and distance criteria).\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2095,\n        \"id\": 484,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a room temperature (298K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"differential scanning calorimetry\",\n        \"primary_unit\": \"mW\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"Differential scanning calorimetry (DSC)\",\n        \"experimental_description\": \"A TA Discovery DSC 2500 was used to carry out low-temperature conventional differential scanning calorimetry (DSC) measurements. The instrument was under helium purge with a 5 K/min ramp from 298 K to 124 K and back to 298 K (with use of an LN2P cooler). Sample powder was loaded into a Tzero Hermetic aluminum pan, with temperature and enthalpy calibrated in advance.\\r\\nA similar instrument was used to perform high-temperature DSC measurements under nitrogen purge. The ramp rate was 5 K/min from 298 K to 603 K. An aluminum pan was hermetically sealed to contain samples.\\r\\nGraph: \\r\\nCooling (5 K/min) of crystal with slow process is the upper graph. Notable points at 183 K and 188 K, where the structure transitions.\\r\\nHeating (5 K/min) of crystal with slow process is the lower graph. Notable points at 203 K and 213 K, where the structure transitions.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"heating\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2113,\n        \"id\": 484,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a room temperature (298K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"relativistic atomic ZORA scalar, \\r\\ninclude spin orbit\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2114,\n        \"id\": 484,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a room temperature (298K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"relativistic atomic ZORA scalar, \\r\\ninclude spin orbit\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2115,\n        \"id\": 484,\n        \"compound_name\": \"S-2-methylbutylammonium lead iodide\",\n        \"formula\": \"C10H28N2PbI4\",\n        \"group\": \"(S-2-MeBA)2PbI4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbI4, lead iodide\",\n        \"iupac\": \"(S)-2-methylbutan-1-aminium lead (II) Iodide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a room temperature (298K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"relativistic atomic ZORA scalar, include spin orbit\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2116,\n        \"id\": 487,\n        \"compound_name\": \"S-2-methylbutylammonium lead bromide\",\n        \"formula\": \"C10H28N2PbBr4\",\n        \"group\": \"(S-2-MeBA)2PbBr4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbBr4, lead bromide\",\n        \"iupac\": \"S-2-methylbutylammonium lead (II) Bromide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a low temperature (100K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 [\\u03b1=0.25, \\u03c9=0.11 \\u00c5^(-1)]\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"relativistic atomic ZORA scalar, include spin orbit\",\n        \"basis_set_definition\": \"FHI-aims intermediate settings\",\n        \"numerical_accuracy\": \"FHI-aims intermediate settings\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbBr2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbBr4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbBr2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbBr4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbBr4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbBr4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2117,\n        \"id\": 487,\n        \"compound_name\": \"S-2-methylbutylammonium lead bromide\",\n        \"formula\": \"C10H28N2PbBr4\",\n        \"group\": \"(S-2-MeBA)2PbBr4\",\n        \"organic\": \"C5H14N\",\n        \"inorganic\": \"PbBr4, lead bromide\",\n        \"iupac\": \"S-2-methylbutylammonium lead (II) Bromide\",\n        \"last_update\": \"2023-02-14\",\n        \"description\": \"This is a low temperature (100K) phase\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"density functional theory\",\n        \"xc_functional\": \"HSE06 [\\u03b1=0.25, \\u03c9=0.11 \\u00c5^(-1)]\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"relativistic atomic ZORA scalar, include_spin_orbit\",\n        \"basis_set_definition\": \"FHI-aims intermediate settings\",\n        \"numerical_accuracy\": \"FHI-aims intermediate settings\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbBr2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbBr4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbBr2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbBr4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbBr4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbBr4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b00847\",\n        \"dataset_ID\": 2118,\n        \"id\": 98,\n        \"compound_name\": \"Bis(1-butylammonium) tris(methylammonium) lead iodide\",\n        \"formula\": \"C11H39N5Pb4I13\",\n        \"group\": \"(BA)2(MA)3Pb4I13, bis(butane-1-aminium) tris(methanaminium) tridecaiodo tetraplumbate(II)\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) tris(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-10-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ruddlesden\\u2212Popper Hybrid Lead Iodide Perovskite 2D Homologous Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2853\",\n        \"pages_end\": \"2867\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead Oxide (PbO), aqueous HI, aqueous H3PO2, n-CH3(CH2)3NH3I , solid CH3NH3Cl\",\n        \"synthesis_product\": \"Black plate-like (BA)2(MA)3Pb4I13 crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of 57% w/w aqueous HI solution (10.0 mL, 76 mmol) and 50% aqueous H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (507 mg, 7.5 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (248 \\u03bcL, 2.5 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time black rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after \\u223c2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence spectroscopy\",\n        \"experimental_description\": \"Oriented rectangular crystals were used in the collection of photoluminescence spectra. Crystals of type (BA)2(MA)3Pb4I13 provided data for the material with n=4. A Horiba LabRam Evolution Raman microscope spectrometer with a diode CW laser (600 g/mm diffraction grating; 473 m, 25 mW) and a Synapse CCD camera carried out measurements. The laser beam was focused at about 1 \\u00b5m spot size was made parallel to the 010 orientation of the crystals. The power output of the laser source was limited to 0.1% of the maximum power output.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"n=4\",\n        \"space_group\": \"Cc2m\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7cc02408h\",\n        \"dataset_ID\": 2121,\n        \"id\": 180,\n        \"compound_name\": \"Bis(phenethylammonium) cadmium iodide\",\n        \"formula\": \"C16H24N2CdI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CdI4, Cadmium iodide\",\n        \"iupac\": \"bis(phenylethanaminium) cadmium iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Powder X-ray diffraction\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"2\\u03b8\",\n        \"secondary_unit\": \"(deg.)\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A near-room-temperature organic\\u2013inorganic hybrid ferroelectric: [C6H5CH2CH2NH3]2[CdI4]\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"5764\",\n        \"pages_end\": \"5766\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",\n        \"synthesis_product\": \"Colorless block-like crystals\",\n        \"synthesis_description\": \"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2\\u2010phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",\n        \"experimental_method\": \"Powder X-ray diffraction\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"experimental\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1038/ncomms16045\",\n        \"dataset_ID\": 2122,\n        \"id\": 495,\n        \"compound_name\": \"Formamidinium methylammonium lead iodide lead bromide\",\n        \"formula\": \"FA0.85MA0.15PbI2.55Br0.45\",\n        \"group\": \"diaminomethanide methanaminium lead iodide lead bromide\",\n        \"organic\": \"CN2H3,CNH6\",\n        \"inorganic\": \"PbI2.55PbBr0.45\",\n        \"iupac\": \"diaminomethanide methanaminium lead iodide lead bromide\",\n        \"last_update\": \"2022-10-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Meniscus-assisted solution printing of large-grained perovskite films for high-efficiency solar cells\",\n        \"journal\": \"nature communications\",\n        \"vol\": \"8\",\n        \"pages_start\": \"16045\",\n        \"pages_end\": \"16045\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"formamidinium iodide, methylammonium bromide, PbI2, PbBr2\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By dissolving formamidinium acetate powder in a 2x molar excess of 57% acid (for FAI) or 48% hydrobromic acid (for MABr) formamidinium iodide (FAI) and methylammonium bromide (MABr) were synthesised. The solution was stirred for 10 minutes at 50\\u00b0 C. A yellow-white powder is formed upon drying at 100\\u00b0 C. This was washed with diethylether and recrystallized twice with ethanol, to form white needle-like crystals. It was dried overnight in a vacuum oven. To form FAPbI3 and FAPbBr3 precursor solutions, FAI and PbI2 or MABr and PbBr2 were dissolved in anhydrous N,N-dimethylformamide (DMF) in a 1:1 molar ratio, at 0.88M of each reagent, to give a 0.88M perovskite precursor solution. Mixtures were made of the FAPbI3 and FAPbBr3 solutions in the required ratios to form the FAPbI3yBr3(1-y) perovskite precursors. The perovskite precursor ink was prepared by dissolving FAI, MABr, PbI2 and PbBr2 (molar ratio of FAI:MABr:PbI2:PbBr2=0.85:0.15:2.55:0.45) in DMSO, and stirred at 60\\u2009\\u00b0C for 2\\u2009h to form 0.25\\u2009M FA0.85MA0.15PbI2.55Br0.45 precursor ink.\",\n        \"experimental_method\": \"UV-Vis photoluminescence\",\n        \"experimental_description\": \"Using a Shimadzu UV2600 spectrophotometer with a photometric integrating sphere, UV-Vis spectra were obtained.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"reference\",\n        \"space_group\": \"P3m1\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1038/ncomms16045\",\n        \"dataset_ID\": 2123,\n        \"id\": 495,\n        \"compound_name\": \"Formamidinium methylammonium lead iodide lead bromide\",\n        \"formula\": \"FA0.85MA0.15PbI2.55Br0.45\",\n        \"group\": \"diaminomethanide methanaminium lead iodide lead bromide\",\n        \"organic\": \"CN2H3,CNH6\",\n        \"inorganic\": \"PbI2.55PbBr0.45\",\n        \"iupac\": \"diaminomethanide methanaminium lead iodide lead bromide\",\n        \"last_update\": \"2022-10-12\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Meniscus-assisted solution printing of large-grained perovskite films for high-efficiency solar cells\",\n        \"journal\": \"nature communications\",\n        \"vol\": \"8\",\n        \"pages_start\": \"16045\",\n        \"pages_end\": \"16045\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"formamidinium iodide, methylammonium bromide, PbI2, PbBr2\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By dissolving formamidinium acetate powder in a 2x molar excess of 57% acid (for FAI) or 48% hydrobromic acid (for MABr) formamidinium iodide (FAI) and methylammonium bromide (MABr) were synthesised. The solution was stirred for 10 minutes at 50\\u00b0 C. A yellow-white powder is formed upon drying at 100\\u00b0 C. This was washed with diethylether and recrystallized twice with ethanol, to form white needle-like crystals. It was dried overnight in a vacuum oven. To form FAPbI3 and FAPbBr3 precursor solutions, FAI and PbI2 or MABr and PbBr2 were dissolved in anhydrous N,N-dimethylformamide (DMF) in a 1:1 molar ratio, at 0.88M of each reagent, to give a 0.88M perovskite precursor solution. Mixtures were made of the FAPbI3 and FAPbBr3 solutions in the required ratios to form the FAPbI3yBr3(1-y) perovskite precursors. The perovskite precursor ink was prepared by dissolving FAI, MABr, PbI2 and PbBr2 (molar ratio of FAI:MABr:PbI2:PbBr2=0.85:0.15:2.55:0.45) in DMSO, and stirred at 60\\u2009\\u00b0C for 2\\u2009h to form 0.25\\u2009M FA0.85MA0.15PbI2.55Br0.45 precursor ink.\",\n        \"experimental_method\": \"UV-Vis Absorbtion\",\n        \"experimental_description\": \"Using a Shimadzu UV2600 spectrophotometer with a photometric integrating sphere, UV-Vis spectra were obtained.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"reference\",\n        \"space_group\": \"P3m1\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.201915422\",\n        \"dataset_ID\": 2124,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observing Defect Passivation of the Grain Boundary with 2-Aminoterephthalic Acid for Efficient and Stable Perovskite Solar Cells\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"4161\",\n        \"pages_end\": \"4167\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, MAI\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"The film is produced using a dynamic two-step deposition method. on a compact TiO2/ATO substrate, a N,N-dimethylformamide (DMF) solution of PbI2 is spin coated at 3000 rpm for 10 s, and an isopropyl alcohol solution of methylammonium iodide (MAI) is immediately added dropwise, while keeping the whole spinning time 20 s prior to the end of spin coating. The yellow PbI2 solution turns to brown immediately and gradually darkens during the spin coating. After annealing at 150 \\u00b0C for 10 min, the as-prepared perovskite film has a shiny black color due to the high visible light absorption and super flat surface. The cross-linking agent 2-aminoterephthalic acid (with different concentrations of 0, 0.2, 0.5, and 1 mg\\u2009mL\\u22121) was immediately spin-coated on the MAPbI3 film and subsequently annealed at 150\\u2009\\u00b0C for 5 min.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"The absorption spectra were collected by a UV-visible spectrophotometer (UV-3600, Shimadzu Corp.)\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"0 mg mL-1 cross-linking agent\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.201915422\",\n        \"dataset_ID\": 2125,\n        \"id\": 24,\n        \"compound_name\": \"Methylammonium lead iodide\",\n        \"formula\": \"CH3NH3PbI3\",\n        \"group\": \"Methanaminium triiodoplumbate(II), MAPI, (MA)PbI3, MAPbI3, (CH3NH3)PbI3\",\n        \"organic\": \"CH6N\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"methanaminium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Observing Defect Passivation of the Grain Boundary with 2-Aminoterephthalic Acid for Efficient and Stable Perovskite Solar Cells\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"59\",\n        \"pages_start\": \"4161\",\n        \"pages_end\": \"4167\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"PbI2, MAI\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"The film is produced using a dynamic two-step deposition method. on a compact TiO2/ATO substrate, a N,N-dimethylformamide (DMF) solution of PbI2 is spin coated at 3000 rpm for 10 s, and an isopropyl alcohol solution of methylammonium iodide (MAI) is immediately added dropwise, while keeping the whole spinning time 20 s prior to the end of spin coating. The yellow PbI2 solution turns to brown immediately and gradually darkens during the spin coating. After annealing at 150 \\u00b0C for 10 min, the as-prepared perovskite film has a shiny black color due to the high visible light absorption and super flat surface. The cross-linking agent 2-aminoterephthalic acid (with different concentrations of 0, 0.2, 0.5, and 1 mg\\u2009mL\\u22121) was immediately spin-coated on the MAPbI3 film and subsequently annealed at 150\\u2009\\u00b0C for 5 min.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"The absorption spectra were collected by a UV-visible spectrophotometer (UV-3600, Shimadzu Corp.)\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"0 mg mL-1 cross-linking agent\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.6b00847\",\n        \"dataset_ID\": 2126,\n        \"id\": 92,\n        \"compound_name\": \"Bis(1-butylammonium) bis(methylammonium) lead iodide\",\n        \"formula\": \"C10H36N4Pb3I10\",\n        \"group\": \"bis(butane-1-aminium) di(methanaminium) decaiodo triplumbate(II), (BA)2(MA)2Pb3I10\",\n        \"organic\": \"C4H12N, CH6N\",\n        \"inorganic\": \"Pb3I10, Lead iodide\",\n        \"iupac\": \"bis(butane-1-aminium) di(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2022-10-18\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"3\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Ruddlesden\\u2212Popper Hybrid Lead Iodide Perovskite 2D Homologous Semiconductors\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"28\",\n        \"pages_start\": \"2853\",\n        \"pages_end\": \"2867\",\n        \"year\": \"2016\",\n        \"synthesis_starting_materials\": \"Lead Oxide (PbO), HI (57% w/w aqueous), H3PO2 (50% aqueous), butylammonium iodide (n-CH3(CH2)3NH3I) , solid CH3NH3Cl\",\n        \"synthesis_product\": \"Dark red plate-like (BA)2(MA)2Pb3I10 crystals\",\n        \"synthesis_description\": \"PbO powder (2232 mg, 10 mmol) was dissolved in a mixture of HI solution (10.0 mL, 76 mmol) and H3PO2 (1.7 mL, 15.5 mmol) by heating to boiling under constant magnetic stirring for about 5 min, which formed a bright yellow solution. Subsequent addition of solid CH3NH3Cl (450 mg, 6.67 mmol) to the hot yellow solution initially caused the precipitation of a black powder, which rapidly redissolved under stirring to afford a clear bright yellow solution. In a separate beaker, n-CH3(CH2)3NH2 (327 \\u03bcL, 3.33 mmol) was neutralized with HI 57% w/w (5 mL, 38 mmol) in an ice bath resulting in a clear pale yellow solution. Addition of the n-CH3(CH2)3NH3I solution to the PbI2 solution initially produced a black precipitate, which was subsequently dissolved under heating the combined solution to boiling. The stirring was then discontinued, and the solution was left to cool to room temperature during which time deep-red/purple rectangular-shaped plates started to crystallize. The precipitation was deemed to be complete after \\u223c2 h. The crystals were isolated by suction filtration and thoroughly dried under reduced pressure.\",\n        \"experimental_method\": \"Photoluminescence spectroscopy\",\n        \"experimental_description\": \"Oriented rectangular crystals were used in the collection of photoluminescence spectra. Crystals of type (BA)2(MA)2Pb3I10 provided data for the material with n=3. A Horiba LabRam Evolution Raman microscope spectrometer with a diode CW laser (600 g/mm diffraction grating; 473 m, 25 mW) and a Synapse CCD camera carried out measurements. The laser beam was focused at about 1 \\u00b5m spot size was made parallel to the 010 orientation of the crystals. The power output of the laser source was limited to 0.1% of the maximum power output.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"cubic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7cc02408h\",\n        \"dataset_ID\": 2127,\n        \"id\": 180,\n        \"compound_name\": \"Bis(phenethylammonium) cadmium iodide\",\n        \"formula\": \"C16H24N2CdI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CdI4, Cadmium iodide\",\n        \"iupac\": \"bis(phenylethanaminium) cadmium iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Powder X-ray diffraction\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"2\\u03b8\",\n        \"secondary_unit\": \"(deg.)\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A near-room-temperature organic\\u2013inorganic hybrid ferroelectric: [C6H5CH2CH2NH3]2[CdI4]\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"5764\",\n        \"pages_end\": \"5766\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",\n        \"synthesis_product\": \"Colorless block-like crystals\",\n        \"synthesis_description\": \"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2\\u2010phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7cc02408h\",\n        \"dataset_ID\": 2128,\n        \"id\": 180,\n        \"compound_name\": \"Bis(phenethylammonium) cadmium iodide\",\n        \"formula\": \"C16H24N2CdI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CdI4, Cadmium iodide\",\n        \"iupac\": \"bis(phenylethanaminium) cadmium iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Powder X-ray diffraction\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"2\\u03b8\",\n        \"secondary_unit\": \"(deg.)\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A near-room-temperature organic\\u2013inorganic hybrid ferroelectric: [C6H5CH2CH2NH3]2[CdI4]\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"5764\",\n        \"pages_end\": \"5766\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",\n        \"synthesis_product\": \"Colorless block-like crystals\",\n        \"synthesis_description\": \"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2\\u2010phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"Manually extracted from publication\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/c7cc02408h\",\n        \"dataset_ID\": 2129,\n        \"id\": 180,\n        \"compound_name\": \"Bis(phenethylammonium) cadmium iodide\",\n        \"formula\": \"C16H24N2CdI4\",\n        \"group\": \"bis(phenylethanaminium) tetraiodocadmate(II), (C6H5CH2CH2NH3)2(CdI4), (PEA)2CdI4\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"CdI4, Cadmium iodide\",\n        \"iupac\": \"bis(phenylethanaminium) cadmium iodide\",\n        \"last_update\": \"2022-01-26\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"differential scanning calorimetry\",\n        \"primary_unit\": \"mW\",\n        \"secondary_name\": \"temperature\",\n        \"secondary_unit\": \"K\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"A near-room-temperature organic\\u2013inorganic hybrid ferroelectric: [C6H5CH2CH2NH3]2[CdI4]\",\n        \"journal\": \"Chemical Communications\",\n        \"vol\": \"53\",\n        \"pages_start\": \"5764\",\n        \"pages_end\": \"5766\",\n        \"year\": \"2017\",\n        \"synthesis_starting_materials\": \"methanol, CdI2 and 2-phenylethylammonium iodide (PEAI; C6H5C2H4NH3I) hydroiodic acid (HI, 57%)\",\n        \"synthesis_product\": \"Colorless block-like crystals\",\n        \"synthesis_description\": \"In dark, 30 mL of methanol, 1.83 g of CdI2, and 2.49 g of PEAI were mixed together and stirred for 20 min. PEAI was synthesized by mixing stoichiometric quantities of 2\\u2010phenylethylamine and HI. The final crystals were obtained in a few days by the slow evaporation of the solution.\",\n        \"experimental_method\": \"Differential scanning calorimetry (DSC)\",\n        \"experimental_description\": \"A powder sample of crystals of (C6H5CH2CH2NH3)2(CdI4) was utilized in this experiment. DSC for heating and cooling was measured at a rate of change of 5 K/min. In the heating cycle, an anomaly occurred at 301 K, and in the cooling graph an anomaly arose at  297 K. A TA DSC Q2000 instrument was used to carry out the experiment.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Cooling\",\n        \"space_group\": \"P 2(1)\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1126/science.aay7044\",\n        \"dataset_ID\": 2131,\n        \"id\": 497,\n        \"compound_name\": \"Formamidinium lead iodide:1.9%MDACl2\",\n        \"formula\": \"CH5N2PbI3:1.9%CH8N2Cl2\",\n        \"group\": \"FAPbI3:MDACl2, FAPbI3:1.9%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\n        \"organic\": \"CH5N2,CH8N2\",\n        \"inorganic\": \"PbI3:Cl-\",\n        \"iupac\": \"Imidoformamidinium lead iodide: methylenediammonium chloride\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient, stable solar cells by using inherent bandgap of \\u03b1-phase formamidinium lead iodide\",\n        \"journal\": \"Science\",\n        \"vol\": \"366\",\n        \"pages_start\": \"749\",\n        \"pages_end\": \"753\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"formamidine acetate salt, hydroiodic acid, lead iodide\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60\\u00b0C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120\\u00b0C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150\\u00b0C. A small amount of MADCl2 was incorporated.\",\n        \"experimental_method\": \"UV-Vis spectroscopy\",\n        \"experimental_description\": \"The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1126/science.aay7044\",\n        \"dataset_ID\": 2132,\n        \"id\": 497,\n        \"compound_name\": \"Formamidinium lead iodide:1.9%MDACl2\",\n        \"formula\": \"CH5N2PbI3:1.9%CH8N2Cl2\",\n        \"group\": \"FAPbI3:MDACl2, FAPbI3:1.9%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\n        \"organic\": \"CH5N2,CH8N2\",\n        \"inorganic\": \"PbI3:Cl-\",\n        \"iupac\": \"Imidoformamidinium lead iodide: methylenediammonium chloride\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2133,\n            2135\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient, stable solar cells by using inherent bandgap of \\u03b1-phase formamidinium lead iodide\",\n        \"journal\": \"Science\",\n        \"vol\": \"366\",\n        \"pages_start\": \"749\",\n        \"pages_end\": \"753\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"formamidine acetate salt, hydroiodic acid, lead iodide\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60\\u00b0C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120\\u00b0C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150\\u00b0C. A small amount of MADCl2 was incorporated.\",\n        \"experimental_method\": \"UV-Vis spectroscopy\",\n        \"experimental_description\": \"The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1126/science.aay7044\",\n        \"dataset_ID\": 2133,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2132,\n            2135\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient, stable solar cells by using inherent bandgap of \\u03b1-phase formamidinium lead iodide\",\n        \"journal\": \"Science\",\n        \"vol\": \"366\",\n        \"pages_start\": \"749\",\n        \"pages_end\": \"753\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"formamidine acetate salt, hydroiodic acid, lead iodide\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60\\u00b0C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120\\u00b0C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150\\u00b0C.\",\n        \"experimental_method\": \"UV-Vis spectroscopy\",\n        \"experimental_description\": \"The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1126/science.aay7044\",\n        \"dataset_ID\": 2134,\n        \"id\": 39,\n        \"compound_name\": \"Formamidinium lead iodide\",\n        \"formula\": \"CH5N2PbI3\",\n        \"group\": \"Methanimidamide triiodoplumbate(II), FAPI, FAPbI3, HC(NH2)2PbI3, (NH2)2CHPbI3\",\n        \"organic\": \"CH5N2\",\n        \"inorganic\": \"PbI3, Lead iodide\",\n        \"iupac\": \"Imidoformamidinium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient, stable solar cells by using inherent bandgap of \\u03b1-phase formamidinium lead iodide\",\n        \"journal\": \"Science\",\n        \"vol\": \"366\",\n        \"pages_start\": \"749\",\n        \"pages_end\": \"753\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"formamidine acetate salt, hydroiodic acid, lead iodide\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60\\u00b0C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120\\u00b0C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150\\u00b0C.\",\n        \"experimental_method\": \"UV-Vis spectroscopy\",\n        \"experimental_description\": \"Steady-state photoluminescence (PL) spectra were measured using a commercial time-correlated single photon counting (TCSPC) setup (FluoTime 300, PicoQuant GmbH) equipped with PMA-C-192-M detector, high-resolution excitation monochromators.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1126/science.aay7044\",\n        \"dataset_ID\": 2135,\n        \"id\": 498,\n        \"compound_name\": \"Formamidinium lead iodide:3.8%MDACl2\",\n        \"formula\": \"CH5N2PbI3:3.8%CH8N2Cl2\",\n        \"group\": \"FAPbI3:MDACl2, FAPbI3:3.8%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\n        \"organic\": \"CH5N2,CH8N2\",\n        \"inorganic\": \"PbI3:Cl-\",\n        \"iupac\": \"Imidoformamidinium lead iodide: methylenediammonium chloride\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2132,\n            2133\n        ],\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient, stable solar cells by using inherent bandgap of \\u03b1-phase formamidinium lead iodide\",\n        \"journal\": \"Science\",\n        \"vol\": \"366\",\n        \"pages_start\": \"749\",\n        \"pages_end\": \"753\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"formamidine acetate salt, hydroiodic acid, lead iodide\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By reaction of 20 of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60\\u00b0C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was created in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120\\u00b0C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150\\u00b0C. A small amount of MADCl2 was incorporated.\",\n        \"experimental_method\": \"UV-Vis absorption\",\n        \"experimental_description\": \"The optical properties of the films were measured using UV-Vis spectroscopy (Shimadzu UV-2600).\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1126/science.aay7044\",\n        \"dataset_ID\": 2136,\n        \"id\": 499,\n        \"compound_name\": \"Formamidinium lead iodide:5.7%MDACl2\",\n        \"formula\": \"CH5N2PbI3:5.7%CH8N2Cl2\",\n        \"group\": \"FAPbI3:MDACl2, FAPbI3:5.7%MDACl2, Formamidium lead(II) triiodide, FAPbI3, MDACl2, formamidium lead iodide methylenediammonium dichloride\",\n        \"organic\": \"CH5N2,CH8N2\",\n        \"inorganic\": \"PbI3:Cl-\",\n        \"iupac\": \"Imidoformamidinium lead iodide: methylenediammonium chloride\",\n        \"last_update\": \"2023-03-05\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Efficient, stable solar cells by using inherent bandgap of \\u03b1-phase formamidinium lead iodide\",\n        \"journal\": \"Science\",\n        \"vol\": \"366\",\n        \"pages_start\": \"749\",\n        \"pages_end\": \"753\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"formamidine acetate, hydroiodic acid (HI, 57 wt% in water), lead iodide, 2-methoxyethanol (anhydrous 99.8%)\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"By reaction of 20 mg of formamidine acetate salt with 30 mL of hydroiodic acid (57 wt% in H20) at 60\\u00b0C and 1-mbar pressure in a 250 ml flask for 1 h, Formamidinium iodide powder was synthesized. The resulting products were dissolved in ethanol, recrystallized from diethyl ether, and finally dried at RT in a vacuum oven for 24 h. Using this synthesized FAI, FAPbI3 powder was synthesized in a 70-mL vial by mixing it 1:1 with lead iodide in 11 ml of 2-methoxyethanol by stirring. The resulting mixture was heated to 120\\u00b0C and then precipitated by retrograde method. The FAPbI3 powder was baked for 30 min at 150\\u00b0C. A small amount of MADCl2 was incorporated.\",\n        \"experimental_method\": \"UV-Vis spectroscopy\",\n        \"experimental_description\": \"The absorption spectrum was measured using Shimadzu UV-2600.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.106.094306\",\n        \"dataset_ID\": 2138,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Transient and steady state magneto-optical studies of CsPbBr3 crystal\",\n        \"journal\": \"American Physical Society\",\n        \"vol\": \"106\",\n        \"pages_start\": \"094306\",\n        \"pages_end\": \"094314\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"CsBr, PbBr2, dimethyl sulfoxide (DMSO\",\n        \"synthesis_product\": \"CsPbBr3 thin film\",\n        \"synthesis_description\": \"A precursor solution, (0.5 M), was made by mixing CsBr (Sigma Aldrich, 0.21 grams), PbBr2 (Sigma Aldrich, 0.37 grams), and dimethyl sulfoxide (DMSO) (2 mL). This solution was then spin cast at 3000 RPM on cleaned glass for 60 seconds. It was then annealed at 106 \\u00b0C for 20 minutes. The resulting film of CsPbBr3 was about 100 nm thick.\",\n        \"experimental_method\": \"Photoluminescence measurement at T = 100 K\",\n        \"experimental_description\": \"The CsPbBr3 thin film is excited at 447 nm with power at 0.5 mW and the intensity of each photon energy emission is measured. This test was performed at temperature T = 100 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"P n m a\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.106.094306\",\n        \"dataset_ID\": 2139,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Transient and steady state magneto-optical studies of CsPbBr3 crystal\",\n        \"journal\": \"American Physical Society\",\n        \"vol\": \"106\",\n        \"pages_start\": \"094306\",\n        \"pages_end\": \"094314\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"CsBr, PbBr2, dimethyl sulfoxide (DMSO\",\n        \"synthesis_product\": \"CsPbBr3 thin film\",\n        \"synthesis_description\": \"A precursor solution, (0.5 M), was made by mixing CsBr (Sigma Aldrich, 0.21 grams), PbBr2 (Sigma Aldrich, 0.37 grams), and dimethyl sulfoxide (DMSO) (2 mL). This solution was then spin cast at 3000 RPM on cleaned glass for 60 seconds. It was then annealed at 106 \\u00b0C for 20 minutes. The resulting film of CsPbBr3 was about 100 nm thick.\",\n        \"experimental_method\": \"Photoluminescence measurement at T = 50 K\",\n        \"experimental_description\": \"The CsPbBr3 thin film is excited at 447 nm with power at 0.5 mW and the intensity of each photon energy emission is measured. This test was performed at temperature of 50 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"10.1103/PhysRevB.106.094306\",\n        \"dataset_ID\": 2140,\n        \"id\": 326,\n        \"compound_name\": \"Cesium lead bromide\",\n        \"formula\": \"CsPbBr3\",\n        \"group\": \"Cesium tribromoplumbate(II), CsPbBr3\",\n        \"organic\": \"None\",\n        \"inorganic\": \"PbBr3, Lead bromide\",\n        \"iupac\": \"Cesium lead(II) bromide\",\n        \"last_update\": \"2022-10-25\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            489\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"photon energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Transient and steady state magneto-optical studies of CsPbBr3 crystal\",\n        \"journal\": \"American Physical Society\",\n        \"vol\": \"106\",\n        \"pages_start\": \"094306\",\n        \"pages_end\": \"094314\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"CsBr, PbBr2, dimethyl sulfoxide (DMSO\",\n        \"synthesis_product\": \"CsPbBr3 thin film\",\n        \"synthesis_description\": \"A precursor solution, (0.5 M), was made by mixing CsBr (Sigma Aldrich, 0.21 grams), PbBr2 (Sigma Aldrich, 0.37 grams), and dimethyl sulfoxide (DMSO) (2 mL). This solution was then spin cast at 3000 RPM on cleaned glass for 60 seconds. It was then annealed at 106 \\u00b0C for 20 minutes. The resulting film of CsPbBr3 was about 100 nm thick.\",\n        \"experimental_method\": \"Photoluminescence measurement at T = 10 K\",\n        \"experimental_description\": \"The CsPbBr3 thin film is excited at 447 nm with power at 0.5 mW and the intensity of each photon energy emission is measured. This test was performed at temperature T = 10 K.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2142,\n        \"id\": 500,\n        \"compound_name\": \"Bis(ethanolammonium) lead iodide\",\n        \"formula\": \"C4H16N2O2PbI4\",\n        \"group\": \"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",\n        \"organic\": \"OC2NH8\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-29\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2147\n        ],\n        \"primary_name\": \"Absorption (Kubelka\\u2212Munk)\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",\n        \"synthesis_product\": \"Red single crystals (EOA2PbI4)\",\n        \"synthesis_description\": \"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 \\u03bcL, 1.3 mmol) is added. This solution is sonicated at room temperature for five minutes. It is then kept at 3 \\u00b0C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"Powder samples of EOA2PbI4 were used to measure absorption. Linear absorptions can be determined from measurements of UV-vis reflection.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Experimental\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2143,\n        \"id\": 500,\n        \"compound_name\": \"Bis(ethanolammonium) lead iodide\",\n        \"formula\": \"C4H16N2O2PbI4\",\n        \"group\": \"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",\n        \"organic\": \"OC2NH8\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-29\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Transient reflectance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",\n        \"synthesis_product\": \"Red single crystals (EOA2PbI4)\",\n        \"synthesis_description\": \"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 \\u03bcL, 1.3 mmol) is added. This solution is sonicated at room temperature  for five minutes. It is then kept at 3 \\u00b0C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",\n        \"experimental_method\": \"Pump-probe spectroscopy\",\n        \"experimental_description\": \"Pump-probe delay spectroscopy was used with single crystals of EOA2PbI4 to measure transient reflectance spectra. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration \\u223c60 fs, \\u223c5 mJ/pulse, and 1 kHz repetition rate) was used for this measurement, and a Helios Ultrafast System was used as the transient reflection spectrometer. A fundamental beam of 800 nm was split into two beams, one being sent to generate the pump pulse and the other focused to create the white light probe (1.6---2.8 eV). The pump beam size was \\u223c590 \\u03bcm and the probe size was \\u223c200 \\u03bcm. The pump beam was sent directly toward the crystal from 90\\u00b0, and the probe beam hit the crystal at 45\\u00b0.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2144,\n        \"id\": 500,\n        \"compound_name\": \"Bis(ethanolammonium) lead iodide\",\n        \"formula\": \"C4H16N2O2PbI4\",\n        \"group\": \"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",\n        \"organic\": \"OC2NH8\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-29\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"transient absorption\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",\n        \"synthesis_product\": \"Red single crystals (EOA2PbI4)\",\n        \"synthesis_description\": \"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 \\u03bcL, 1.3 mmol) is added. This solution is sonicated at room temperature  for five minutes. It is then kept at 3 \\u00b0C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",\n        \"experimental_method\": \"Pump-probe spectroscopy\",\n        \"experimental_description\": \"Pump-probe delay spectroscopy was used with single crystals of EOA2PbI4 to measure transient reflectance spectra. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration \\u223c60 fs, \\u223c5 mJ/pulse, and 1 kHz repetition rate) was used for this measurement, and a Helios Ultrafast System was used as the transient reflection spectrometer. A fundamental beam of 800 nm was split into two beams, one being sent to generate the pump pulse and the other focused to create the white light probe (1.6---2.8 eV). The pump beam size was \\u223c590 \\u03bcm and the probe size was \\u223c200 \\u03bcm. The pump beam was sent directly toward the crystal from 90\\u00b0, and the probe beam hit the crystal at 45\\u00b0. A Kramers---Kronig transformation was used to obtain the change in absorbance of the reflected light.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2146,\n        \"id\": 292,\n        \"compound_name\": \"Bis(3-iodopropylammonium) lead iodide\",\n        \"formula\": \"C6H18N2PbI6\",\n        \"group\": \"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",\n        \"organic\": \"C3H9NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(3-iodopropylaminium) lead (II) iodide\",\n        \"last_update\": \"2023-02-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2150\n        ],\n        \"primary_name\": \"Absorption (Kubelka\\u2212Munk)\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"Elliot Fit\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2147,\n        \"id\": 500,\n        \"compound_name\": \"Bis(ethanolammonium) lead iodide\",\n        \"formula\": \"C4H16N2O2PbI4\",\n        \"group\": \"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",\n        \"organic\": \"OC2NH8\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-29\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2142\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"meV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"lead iodide (PbI2), hydroiodic acid (HI, 57% w/w aqueous, stabilized with H3PO2), ethanolamine (EOA), diethyl ether\",\n        \"synthesis_product\": \"Red single crystals (EOA2PbI4)\",\n        \"synthesis_description\": \"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 \\u03bcL, 1.3 mmol) is added. This solution is sonicated at room temperature for five minutes. It is then kept at 3 \\u00b0C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"Powder samples of EOA2PbI4 were used to measure absorption. Linear absorptions can be determined from measurements of UV-vis reflection, and a 2D Elliot formula was used to create a fit for the data. This formula can be found in the supporting information of the referenced publication and the files attached to this dataset. The formula can extract the exciton binding energy of this material. The analysis yields an exciton binding energy of \\u2248 46 meV.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/B917824D\",\n        \"dataset_ID\": 2148,\n        \"id\": 500,\n        \"compound_name\": \"Bis(ethanolammonium) lead iodide\",\n        \"formula\": \"C4H16N2O2PbI4\",\n        \"group\": \"EOA2PbI4, bis(ethanolammonium) lead iodide, (C2H8ON)2PbI4\",\n        \"organic\": \"OC2NH8\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2022-11-29\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Effect of heteroatoms in the inorganic\\u2013organic layered perovskite-type hybrids [(ZCnH2nNH3)2PbI4], n = 2, 3, 4, 5, 6; Z = OH, Br and I; and [(H3NC2H4S2C2H4NH3)PbI4]\",\n        \"journal\": \"CrystEngComm\",\n        \"vol\": \"12\",\n        \"pages_start\": \"1290\",\n        \"pages_end\": \"1301\",\n        \"year\": \"2010\",\n        \"synthesis_starting_materials\": \"PbI2, HI, EOA, diethyl ether\",\n        \"synthesis_product\": \"Red single crystals (EOA2PbI4)\",\n        \"synthesis_description\": \"PbI2 (0.16 g, 0.35 mmol) is dissolved in HI solution (1 mL). Then, EOA (80 \\u03bcL, 1.3 mmol) is added. This solution is sonicated at room temperature  for five minutes. It is then kept at 3 \\u00b0C in a fridge. Later, red single crystals can be filtered and washed with diethyl ether. They are vacuum dried overnight.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single crystal X-ray diffraction data was collected at 173 K using a Bruker SMART 1K CCD detectordiffractometer with graphite monochromated Mo K\\u03b1 radiation (\\u03bb = 0.71073 \\u00c5). Software used in this process was Bruker SAINT+ and SHELXS-97. Further data was gathered using PLATON, WinGx, ORTEP, and DIAMOND.\",\n        \"physical_property\": \"173.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2150,\n        \"id\": 292,\n        \"compound_name\": \"Bis(3-iodopropylammonium) lead iodide\",\n        \"formula\": \"C6H18N2PbI6\",\n        \"group\": \"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",\n        \"organic\": \"C3H9NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(3-iodopropylaminium) lead (II) iodide\",\n        \"last_update\": \"2023-02-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2146\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"meV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1038/s41467-020-18015-5\",\n        \"dataset_ID\": 2151,\n        \"id\": 502,\n        \"compound_name\": \"Cesium lead iodide bromide\",\n        \"formula\": \"CsPbBrI2\",\n        \"group\": \"Cesium lead(II) bromide diiodide, cesium bromo diiodoplumbate\",\n        \"organic\": \"none\",\n        \"inorganic\": \"CsPbBrI2\",\n        \"iupac\": \"Cesium lead bromide diiodide\",\n        \"last_update\": \"2022-11-29\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Surface chelation of cesium halide perovskite by dithiocarbamate for efficient and stable solar cells\",\n        \"journal\": \"Nature communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4237\",\n        \"pages_end\": \"4237\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"PbI2, PbBr2, CsI, DMSO\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"235.5 mg PbI2, 187 mg PbBr2, and 272 mg CsI were dissolved in DMSO to a final volume of 1 mL. This was stirred overnight at room temperature.\",\n        \"experimental_method\": \"UV-Vis spectroscopy\",\n        \"experimental_description\": \"UV\\u2013Vis spectra were collected using a Cary 500 UV\\u2013Vis\\u2013NIR spectrophotometer in air ambient environments.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"not aged\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2153,\n        \"id\": 293,\n        \"compound_name\": \"Bis(4-iodobutylammonium) lead iodide\",\n        \"formula\": \"C8H22N2PbI6\",\n        \"group\": \"(I(CH2)4NH3)2PbI4, bis(4-iodobutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C4H11NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(4-iodobutylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2154\n        ],\n        \"primary_name\": \"Absorption (Kubelka\\u2212Munk)\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PbI2, HI(47%), butanolamine (HOC4H8NH2), ethyl acetate\",\n        \"synthesis_product\": \"Yellow crystals of bis(4-iodobutylammonium) lead iodide\",\n        \"synthesis_description\": \"PbI2 (0.178 mmol; 0.082 g) was dissolved in 1 mL HI solution. Then HOC4H8NH2 (0.449 mmol; 0.040 g) was added. The precipitate was dissolved at 3 mL ethyl acetate and was kept undisturbed at room temperature. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom.\",\n        \"experimental_method\": \"Reflectance spectroscopy\",\n        \"experimental_description\": \"Powder samples of BIA2PbI4 were tested for absorption. Linear absorption was determined through UV-vis reflection. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration about 60 fs, about 5 mJ/pulse) was used to test the powder sample.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"experimental\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1021/jacs.1c08514\",\n        \"dataset_ID\": 2154,\n        \"id\": 293,\n        \"compound_name\": \"Bis(4-iodobutylammonium) lead iodide\",\n        \"formula\": \"C8H22N2PbI6\",\n        \"group\": \"(I(CH2)4NH3)2PbI4, bis(4-iodobutylaminium) tetraiodoplumbate(II)\",\n        \"organic\": \"C4H11NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(4-iodobutylaminium) lead (II) iodide\",\n        \"last_update\": \"2021-12-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2153\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"meV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Tuning Spin-Polarized Lifetime in Two-Dimensional Metal\\u2212Halide Perovskite through Exciton Binding Energy\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"19438\",\n        \"pages_end\": \"19445\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PbI2, HI(47%), butanolamine (HOC4H8NH2), ethyl acetate\",\n        \"synthesis_product\": \"Yellow crystals of bis(4-iodobutylammonium) lead iodide\",\n        \"synthesis_description\": \"PbI2 (0.178 mmol; 0.082 g) was dissolved in 1 mL HI solution. Then HOC4H8NH2 (0.449 mmol; 0.040 g) was added. The precipitate was dissolved at 3 mL ethyl acetate and was kept undisturbed at room temperature. It is assumed that there was a substitution reaction that took place where the amine had an alcohol group substituted with an iodide atom.\",\n        \"experimental_method\": \"Reflectance spectroscopy\",\n        \"experimental_description\": \"Powder samples of BIA2PbI4 were tested for absorption. Linear absorption was determined through UV-vis reflection. A Ti:sapphire laser amplifier (Coherent Astrella, 800 nm, pulse duration about 60 fs, about 5 mJ/pulse) was used to test the powder sample.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1038/s41467-020-18015-5\",\n        \"dataset_ID\": 2156,\n        \"id\": 502,\n        \"compound_name\": \"Cesium lead iodide bromide\",\n        \"formula\": \"CsPbBrI2\",\n        \"group\": \"Cesium lead(II) bromide diiodide, cesium bromo diiodoplumbate\",\n        \"organic\": \"none\",\n        \"inorganic\": \"CsPbBrI2\",\n        \"iupac\": \"Cesium lead bromide diiodide\",\n        \"last_update\": \"2022-11-29\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Surface chelation of cesium halide perovskite by dithiocarbamate for efficient and stable solar cells\",\n        \"journal\": \"Nature communications\",\n        \"vol\": \"11\",\n        \"pages_start\": \"4237\",\n        \"pages_end\": \"4237\",\n        \"year\": \"2020\",\n        \"synthesis_starting_materials\": \"Pb(DDTC)2, PbI2, PbBr2, CsI, DMSO\",\n        \"synthesis_product\": \"thin film\",\n        \"synthesis_description\": \"Synthesis of Pb(DDTC)2 by addition of 20.0 M NaDDTC\\u00b73H2O\\r\\naqueous solution to Pb(NO3)2 aqueous solution (10.0 M) during constant stirring at room temperature. After 30 minutes, filtering of yellow precipitate and washing four times with water, drying at 60\\u00b0C in oven. Dissolution of 30.22 mg Pb(DDTC)2 into 2.0 mL DMSO\\r\\nsolution to result in Pb(DDTC)2-DMSO solution (0.03 M).  235.5 mg PbI2, 187\\r\\nmg PbBr2, and 272 mg CsI were dissolved in DMSO and Pb(DDTC)2-DMSO\\r\\nmixed solution to a final volume of 1 mL with desired Pb(DDTC)2 concentration. This was stirred overnight at room temperature. Then thin films were deposited onto glass substrates.\",\n        \"experimental_method\": \"Steady-state photoluminescence\",\n        \"experimental_description\": \"The steady-state PL were acquired by Fluorolog-3-p spectrophotometer in air at room temperature. PL excitation wavelength was 380 nm.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"pristine\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2157,\n        \"id\": 504,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",\n        \"formula\": \"C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"group\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.3, y = 0.3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2165\n        ],\n        \"primary_name\": \"photoluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",\n        \"experimental_method\": \"Photoluminescence spectroscopy\",\n        \"experimental_description\": \"Photoluminescence spectra were measured on crystal films using a Horiba iHR320 spectroscopy device and a 337 nm SRS NL100 nitrogen laser.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/anie.201910800\",\n        \"dataset_ID\": 2158,\n        \"id\": 38,\n        \"compound_name\": \"Cesium lead iodide\",\n        \"formula\": \"CsPbI3\",\n        \"group\": \"cesium lead iodide, cesium triiodoplumbate(II)\",\n        \"organic\": \"None\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            516,\n            517,\n            518,\n            519,\n            520,\n            521,\n            522\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"The Role of Dimethylammonium Iodide in CsPbI3 Perovskite Fabrication: Additive or Dopant?\",\n        \"journal\": \"Angewandte Chemie International Edition\",\n        \"vol\": \"58\",\n        \"pages_start\": \"16691\",\n        \"pages_end\": \"16696\",\n        \"year\": \"2019\",\n        \"synthesis_starting_materials\": \"CsI, PbI2, DMAI\",\n        \"synthesis_product\": \"thin film of CsIPbI3:xDMAI\",\n        \"synthesis_description\": \"CsI, PbI2, xDMAI (Dimethylammonium Iodide) were dissolved at a 1:1:x molar ratio (with x = 0.5, 0.7, 1.0 and 1.5) in DMF to prepare the CsPbI3:xDMAI-precursor. The active layer was spin-coated onto a 70\\u00b0C warm c-TiO2/FTO substrate at 3000 rpm for 30s. Annealing was done at 150\\u00b0C for 2 minutes for x = 0.5 and for 10 minutes for x = 0.7, as well as at 210\\u00b0C for 5 minutes for x = 1.0 and 1.5. Experiments were done in a dry box with 5-10% RH.\",\n        \"experimental_method\": \"UV-Vis spectroscopy\",\n        \"experimental_description\": \"None stated\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"no doping\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manually entered\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2159,\n        \"id\": 504,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",\n        \"formula\": \"C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"group\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.3, y = 0.3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Electroluminescence\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",\n        \"experimental_method\": \"Electroluminescence spectroscopy\",\n        \"experimental_description\": \"Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2were prepared for this experiment.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2160,\n        \"id\": 504,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",\n        \"formula\": \"C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"group\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.3, y = 0.3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2161\n        ],\n        \"primary_name\": \"external quantum efficiency (EQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"Current Density\",\n        \"secondary_unit\": \"mA/cm2\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",\n        \"experimental_method\": \"Electroluminescence spectroscopy\",\n        \"experimental_description\": \"Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2 were prepared for this experiment. The external quantum efficiency can then be calculated using the EL spectrum with the Lambertian profile.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2161,\n        \"id\": 504,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",\n        \"formula\": \"C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"group\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.3, y = 0.3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2160\n        ],\n        \"primary_name\": \"external quantum efficiency (EQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",\n        \"experimental_method\": \"Electroluminescence spectroscopy\",\n        \"experimental_description\": \"Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2were prepared for this experiment. The external quantum efficiency can then be calculated using the EL spectrum with the Lambertian profile.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2162,\n        \"id\": 505,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.2, y = 0.4\",\n        \"formula\": \"C16H24N2Rb0.2Cs0.8PbBr2.6Cl0.4\",\n        \"group\": \"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4, (C8H12N)2RbCsPbBrCl\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.2Cs0.8PbBr2.6Cl0.4\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.2, y = 0.4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M). Different fractional compounds were created by mixing these solutions in certain ratios.\",\n        \"experimental_method\": \"Photoluminescence spectroscopy\",\n        \"experimental_description\": \"Photoluminescence quantum efficiency (PLQE) was measured through the use of a Labsphere QE sphere, or an integrating sphere, connected to an Ocean Optics QEpro, which is a photoluminescence spectrometer. The excitation source was a 405 nm continuous laser at an intensity of 0.17 mW/(cm^2). Experiments were performed at room temperature with perovskite films on glass.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.abq4524\",\n        \"dataset_ID\": 2163,\n        \"id\": 506,\n        \"compound_name\": \"Tributyl(methyl)phosphonium lead iodide\",\n        \"formula\": \"C13H30PPbI3\",\n        \"group\": \"tributyl(methyl)phosphonium lead iodide, TPPbI3\",\n        \"organic\": \"C13H30P\",\n        \"inorganic\": \"PbI3, lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2164\n        ],\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"O.D.\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Perovskite grain wrapping by converting interfaces and grain boundaries into robust and water-insoluble low-dimensional perovskites\",\n        \"journal\": \"Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"eabq4524\",\n        \"pages_end\": \"eabq4525\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"TPI, PbI2, dimethylformamide (DMF)\",\n        \"synthesis_product\": \"Tributyl(methyl)phosphonium lead iodide film\",\n        \"synthesis_description\": \"PbI2 (0.5 mol) and TPI (0.5 mol) were both dissolved in DMF (1 mL). The resulting solution (30 \\u03bcL) was dropped onto a glass surface. Spin-coating was performed at 5000 rpm for 30 seconds, then the film was annealed at 100\\u00b0C for 5 minutes.\",\n        \"experimental_method\": \"UV-Vis Spectroscopy\",\n        \"experimental_description\": \"The absorbance spectrum of TPPbI3 films were recorded using UV-Vis spectroscopy, no information about equipment given.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1126/sciadv.abq4524\",\n        \"dataset_ID\": 2164,\n        \"id\": 506,\n        \"compound_name\": \"Tributyl(methyl)phosphonium lead iodide\",\n        \"formula\": \"C13H30PPbI3\",\n        \"group\": \"tributyl(methyl)phosphonium lead iodide, TPPbI3\",\n        \"organic\": \"C13H30P\",\n        \"inorganic\": \"PbI3, lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 1,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2163\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Perovskite grain wrapping by converting interfaces and grain boundaries into robust and water-insoluble low-dimensional perovskites\",\n        \"journal\": \"Science\",\n        \"vol\": \"8\",\n        \"pages_start\": \"eabq4524\",\n        \"pages_end\": \"eabq4525\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"TPI, PbI2, dimethylformamide (DMF)\",\n        \"synthesis_product\": \"Tributyl(methyl)phosphonium lead iodide film\",\n        \"synthesis_description\": \"PbI2 (0.5 mol) and TPI (0.5 mol) were both dissolved in DMF (1 mL). The resulting solution (30 \\u03bcL) was dropped onto a glass surface. Spin-coating was performed at 5000 rpm for 30 seconds, then the film was annealed at 100\\u00b0C for 5 minutes.\",\n        \"experimental_method\": \"UV-Vis Spectroscopy\",\n        \"experimental_description\": \"The absorbance spectrum of TPPbI3 films were recorded using UV-Vis spectroscopy, no information about equipment given.\\r\\nThe band gap was determined from the absorption spectrum.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2165,\n        \"id\": 504,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.3, y = 0.3\",\n        \"formula\": \"C16H24N2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"group\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3, (C8H12N)2Rb0.3Cs0.7PbBr2.7Cl0.3\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.3Cs0.7PbBr2.7Cl0.3, rubidium cesium lead bromide iodide\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.3, y = 0.3\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2157\n        ],\n        \"primary_name\": \"photoluminescence quantum efficiency (PLQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.3Cs0.7PbBr2.7Cl0.3 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M).\",\n        \"experimental_method\": \"Photoluminescence spectroscopy\",\n        \"experimental_description\": \"Photoluminescence spectra were measured on crystal films using a Horiba iHR320 spectroscopy device and a 337 nm SRS NL100 nitrogen laser.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2166,\n        \"id\": 505,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.2, y = 0.4\",\n        \"formula\": \"C16H24N2Rb0.2Cs0.8PbBr2.6Cl0.4\",\n        \"group\": \"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4, (C8H12N)2RbCsPbBrCl\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.2Cs0.8PbBr2.6Cl0.4\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.2, y = 0.4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2167\n        ],\n        \"primary_name\": \"electroluminescence (EL) intensity normalized\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M). Different fractional compounds were created by mixing these solutions in certain ratios.\",\n        \"experimental_method\": \"Electroluminescence spectroscopy\",\n        \"experimental_description\": \"Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2 were prepared for this experiment.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1002/adma.202100783\",\n        \"dataset_ID\": 2167,\n        \"id\": 505,\n        \"compound_name\": \"Bis(phenethylammonium) rubidium(x) cesium(1-x) lead bromide(3-y) chloride(y): x = 0.2, y = 0.4\",\n        \"formula\": \"C16H24N2Rb0.2Cs0.8PbBr2.6Cl0.4\",\n        \"group\": \"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4, (C8H12N)2RbCsPbBrCl\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"Rb0.2Cs0.8PbBr2.6Cl0.4\",\n        \"iupac\": \"bis(phenethylaminium) rubidium cesium lead(II) bromide chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"x = 0.2, y = 0.4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2166\n        ],\n        \"primary_name\": \"external quantum efficiency (EQE)\",\n        \"primary_unit\": \"%\",\n        \"secondary_name\": \"Current Density\",\n        \"secondary_unit\": \"mA/cm2\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Highly Efficient Pure-Blue Light-Emitting Diodes Based on Rubidium and Chlorine Alloyed Metal Halide Perovskite\",\n        \"journal\": \"Advanced Materials\",\n        \"vol\": \"33\",\n        \"pages_start\": \"2100783\",\n        \"pages_end\": \"2100783\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"PEA (phenethylamine), HCl (hydrochloric acid), CsBr, PbBr2, PbCl2, YCl3, RbBr, DMSO (dimethyl sulfoxide)\",\n        \"synthesis_product\": \"PEA2Rb0.2Cs0.8PbBr2.6Cl0.4 film\",\n        \"synthesis_description\": \"First, phenethylamine and hydrochloric acid were used to create a solution of PEACl, or phenethylammonium chloride. CsBr (106.4 mg) and PbBr2 (183.5 mg) were dissolved in DMSO (2 mL) to create a CsPbBr3 solution (0.25 M). Similarly, CsBr (106.4 mg), PbBr2 (137.6 mg), and PbCl2 (34.8 mg) were mixed in 2 mL DMSO to form a solution of CsPbBr2.5Cl0.5. Next, 82.7 mg of RbBr was mixed with 183.5 mg of PbBr2 in 2 mL DMSO. Then, PEACl (157.6 mg) was mixed in 1 mL of DMSO to create a PEACl solution (1 M), and YCl3 (39 mg) was mixed in 2 mL DMSO to create a YCl3 solution (0.1 M). Different fractional compounds were created by mixing these solutions in certain ratios.\",\n        \"experimental_method\": \"Electroluminescence spectroscopy\",\n        \"experimental_description\": \"Electroluminescence was measured using a Horiba iHR320 Photoluminescence Spectroscopy device. Crystal films of PEA2 were prepared for this experiment. The external quantum efficiency can then be calculated using the EL spectrum with the Lambertian profile.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2168,\n        \"id\": 507,\n        \"compound_name\": \"4-(R)-(+)-\\u03b2-methylphenethylammonium indium antimony chloride\",\n        \"formula\": \"C36H52N4In0.89Sb1.11Cl10\",\n        \"group\": \"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-\\u03b2-methylphenethylamine)4In2(1-x)Sb2xCl10\",\n        \"organic\": \"C9H13N\",\n        \"inorganic\": \"In0.89Sb1.11Cl10\",\n        \"iupac\": \"(R)-(+)-\\u03b2-methylphenethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"In2O3, MPA, HCl\",\n        \"synthesis_product\": \"Single crystals of 4-(R)-(+)-\\u03b2-methylphenethylamine indium antimony chloride\",\n        \"synthesis_description\": \"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 \\u03bcL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Atomic structure data was collected on a Bruker D8 Venture diffractometer with Mo-K\\u03b1 radiation of \\u03bb = 0.71073 \\u00c5 at 173 Kelvin. Bruker software (APEX3), Olex2, and SHELXL methods were used in data reduction and structure analysis.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2169,\n        \"id\": 13,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead chloride\",\n        \"formula\": \"C14H20N2PbCl4\",\n        \"group\": \"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2173\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2173,\n        \"id\": 13,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead chloride\",\n        \"formula\": \"C14H20N2PbCl4\",\n        \"group\": \"bis(phenylmethanaminium) tetrachloroplumbate(II), (PMA)2PbCl4, (C6H5CH2NH3)2PbCl4, (C7H10N)2PbCl4, (C7H7NH3)2PbCl4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2169\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.2c05574\",\n        \"dataset_ID\": 2179,\n        \"id\": 506,\n        \"compound_name\": \"Tributyl(methyl)phosphonium lead iodide\",\n        \"formula\": \"C13H30PPbI3\",\n        \"group\": \"tributyl(methyl)phosphonium lead iodide, TPPbI3\",\n        \"organic\": \"C13H30P\",\n        \"inorganic\": \"PbI3, lead iodide\",\n        \"iupac\": \"\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"3x4x4\",\n        \"level_of_relativity\": \"relativistic atomic ZORA scalar, include spin orbit\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Kinetically Controlled Structural Transitions in Layered Halide-Based Perovskites: An Approach to Modulate Spin Splitting\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"144 (33)\",\n        \"pages_start\": \"15223\",\n        \"pages_end\": \"15235\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"S-2-MeBA, PbI2, HI, dimethylformamide (DMF), dichloromethane (DCM), ethyl ether\",\n        \"synthesis_product\": \"yellow flaky single crystals (S-2-MeBA)2PbI4\",\n        \"synthesis_description\": \"Add (S-2-MeBA) (0.25 mmol) and PbI2 (0.125 mmol) to 0.8 mL of an aqueous HI solution. Obtain a clear solution at 95 degrees Celsius, then cool to room temperature at a rate of 2 degrees Celsius per hour. The cooling process yields about 0.07 grams of (S-2-MeBA)2PbI4 crystals. Then, dissolve 0.03 g of the obtained crystals in dimethylformamide (DMF) (0.8 mol/L) in a small uncovered vial, and place it in a larger vial holding dichloromethane (DCM). Over a week-long period, the DCM vapors diffuse into the vial with the DMF solution and produce yellow flaky single crystals ((S-2-MeBA)2PbI4) as well as S-2-MeBA salt, light-yellow needle-shaped crystals. The crystals were filtered, washed with ethyl ether, and vacuum-dried. The (S-2-MeBA)2PbI4 crystals can be separated from the salt crystals under a microscope, and they were then used for single-crystal X-ray diffraction (SC-XRD).\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2180,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2181\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2181,\n        \"id\": 8,\n        \"compound_name\": \"Bis(Phenylmethylammonium) lead bromide\",\n        \"formula\": \"C14H20N2PbBr4\",\n        \"group\": \"bis(benzylaminium) tetrabromoplumbate(II), (PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"(PMA)2PbBr4, (C6H5CH2NH3)2PbBr4, (C7H10N)2PbBr4, (C7H7NH3)2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2180\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2182,\n        \"id\": 12,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2183\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2183,\n        \"id\": 12,\n        \"compound_name\": \"Bis(phenylmethylammonium) lead iodide\",\n        \"formula\": \"C14H20N2PbI4\",\n        \"group\": \"bis(phenylmethanaminium) tetraiodoplumbate(II), (PMA)2PbI4, (C7H7NH3)2PbI4, (C7H10N)2PbI4, (C6H5CH2NH3)2PbI4\",\n        \"organic\": \"C7H10N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(phenylmethanaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2182\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2184,\n        \"id\": 14,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead chloride\",\n        \"formula\": \"C22H24N2PbCl4\",\n        \"group\": \"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2185\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2185,\n        \"id\": 14,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead chloride\",\n        \"formula\": \"C22H24N2PbCl4\",\n        \"group\": \"bis(2-(napthalen-2-yl)methanaminium) tetrachloroplumbate(II), (NMA)2PbCl4, (C11H9NH3)2PbCl4, (C11H12N)2PbCl4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2184\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2186,\n        \"id\": 7,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead bromide\",\n        \"formula\": \"C22H24N2PbBr4\",\n        \"group\": \"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"NMA2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2187\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2187,\n        \"id\": 7,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead bromide\",\n        \"formula\": \"C22H24N2PbBr4\",\n        \"group\": \"1-(2-naphthyl)methylaminium tetrabromoplumbate(II), NMA2PbBr4, (C11H9NH3)2PbBr4, (C11H12N)2PbBr4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"NMA2PbBr4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2186\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2188,\n        \"id\": 27,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead iodide\",\n        \"formula\": \"C22H24N2PbI4\",\n        \"group\": \"Bis(1-(2-naphthyl)methylaminium) tetraiodoplumbate(II), NMA2PbI4, (C11H9NH3)2PbI4, (C11H12N)2PbI4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2189\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2189,\n        \"id\": 27,\n        \"compound_name\": \"Bis(1-(2-naphthyl)methylammonium) lead iodide\",\n        \"formula\": \"C22H24N2PbI4\",\n        \"group\": \"Bis(1-(2-naphthyl)methylaminium) tetraiodoplumbate(II), NMA2PbI4, (C11H9NH3)2PbI4, (C11H12N)2PbI4\",\n        \"organic\": \"C11H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"1-(2-naphthyl)methylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2188\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2191,\n        \"id\": 4,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead chloride\",\n        \"formula\": \"C30H28N2PbCl4\",\n        \"group\": \"bis(anthracen-1-ylmethanaminium) tetrachloroplumbate(II), AMA2PbCl4, (C15H11NH3)2PbCl4, (C15H14N)2PbCl4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(anthracen-1-ylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"AMA2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": [\n            2192\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2192,\n        \"id\": 4,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead chloride\",\n        \"formula\": \"C30H28N2PbCl4\",\n        \"group\": \"bis(anthracen-1-ylmethanaminium) tetrachloroplumbate(II), AMA2PbCl4, (C15H11NH3)2PbCl4, (C15H14N)2PbCl4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbCl4, Lead chloride\",\n        \"iupac\": \"bis(anthracen-1-ylmethanaminium) lead(II) chloride\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"AMA2PbCl4\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": [\n            2191\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2193,\n        \"id\": 25,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead bromide\",\n        \"formula\": \"C30H28N2PbBr4\",\n        \"group\": \"Anthracenidemethylaminium tetrabromoplumbate(II), AMA2PbBr4, (C15H11NH3)2PbBr4, (C15H14N)2PbBr4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": [\n            2194\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2194,\n        \"id\": 25,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead bromide\",\n        \"formula\": \"C30H28N2PbBr4\",\n        \"group\": \"Anthracenidemethylaminium tetrabromoplumbate(II), AMA2PbBr4, (C15H11NH3)2PbBr4, (C15H14N)2PbBr4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) bromide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [\n            1\n        ],\n        \"Related_data_setID\": [\n            2193\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2195,\n        \"id\": 26,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead iodide\",\n        \"formula\": \"C30H28N2PbI4\",\n        \"group\": \"anthracenidemethylaminium tetraiodoplumbate(II), AMA2PbI4, (C15H11NH3)2PbI4, (C15H14N)2PbI4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2196\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2196,\n        \"id\": 26,\n        \"compound_name\": \"Bis(2-anthrylmethylammonium) lead iodide\",\n        \"formula\": \"C30H28N2PbI4\",\n        \"group\": \"anthracenidemethylaminium tetraiodoplumbate(II), AMA2PbI4, (C15H11NH3)2PbI4, (C15H14N)2PbI4\",\n        \"organic\": \"C15H14N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"anthracenidemethylaminium lead(II) iodide\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2195\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2197,\n        \"id\": 508,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead chloride\",\n        \"formula\": \"(C18H11CH2NH3)2PbCl4\",\n        \"group\": \"(TMA)2PbCl4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbCl4\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2198\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2198,\n        \"id\": 508,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead chloride\",\n        \"formula\": \"(C18H11CH2NH3)2PbCl4\",\n        \"group\": \"(TMA)2PbCl4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbCl4\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) chloride\",\n        \"last_update\": \"2023-01-17\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2197\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2199,\n        \"id\": 28,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead bromide\",\n        \"formula\": \"C38H32N2PbBr4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetrabromoplumbate(II), (TMA)2PbBr4, (C18H11CH2NH3)2PbBr4, (C19H16N)2PbBr4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2200\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2200,\n        \"id\": 28,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead bromide\",\n        \"formula\": \"C38H32N2PbBr4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetrabromoplumbate(II), (TMA)2PbBr4, (C18H11CH2NH3)2PbBr4, (C19H16N)2PbBr4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbBr4, Lead bromide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) bromide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2199\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2201,\n        \"id\": 29,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead iodide\",\n        \"formula\": \"C38H32N2PbI4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetraiodoplumbate(II), (TMA)2PbI4, (C18H11CH2NH3)2PbI4, (C19H16N)2PbI4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2202\n        ],\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"PBE+TS\",\n        \"k_point_grid\": \"2x5x5\",\n        \"level_of_relativity\": \"atomic ZORA\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"NA\",\n        \"dataset_ID\": 2202,\n        \"id\": 29,\n        \"compound_name\": \"Bis(1-tetracenemethylammonium) lead iodide\",\n        \"formula\": \"C38H32N2PbI4\",\n        \"group\": \"bis(1-tetracenemethylaminium) tetraiodoplumbate(II), (TMA)2PbI4, (C18H11CH2NH3)2PbI4, (C19H16N)2PbI4\",\n        \"organic\": \"C19H16N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(1-tetracenemethylaminium) lead(II) iodide\",\n        \"last_update\": \"2022-08-04\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2201\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Density Functional Theory (DFT)\",\n        \"xc_functional\": \"HSE06 \\u03b1 = 0.25, \\u03c9 = 0.11/bohr\",\n        \"k_point_grid\": \"3x3x3\",\n        \"level_of_relativity\": \"atomic ZORA with spin-orbit coupling\",\n        \"basis_set_definition\": \"intermediate\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Structural and Electronic Tunability of Acene Alkylamines based Layered Hybrid Organic-Inorganic Perovskites from First Principles\",\n        \"journal\": \"To be published\",\n        \"vol\": \"NA\",\n        \"pages_start\": \"NA\",\n        \"pages_end\": \"NA\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"tetragonal\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2203,\n        \"id\": 507,\n        \"compound_name\": \"4-(R)-(+)-\\u03b2-methylphenethylammonium indium antimony chloride\",\n        \"formula\": \"C36H52N4In0.89Sb1.11Cl10\",\n        \"group\": \"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-\\u03b2-methylphenethylamine)4In2(1-x)Sb2xCl10\",\n        \"organic\": \"C9H13N\",\n        \"inorganic\": \"In0.89Sb1.11Cl10\",\n        \"iupac\": \"(R)-(+)-\\u03b2-methylphenethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"In2O3, MPA, HCl\",\n        \"synthesis_product\": \"Powder of 4-(R)-(+)-\\u03b2-methylphenethylamine indium antimony chloride\",\n        \"synthesis_description\": \"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 \\u03bcL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling. For UV-vis spectroscopy, these single crystals were then ground into a powder.\",\n        \"experimental_method\": \"UV-vis spectroscopy\",\n        \"experimental_description\": \"UV-vis spectroscopy was employed to record the absorbance of powder samples of the crystal, which were adhered onto a barium sulfate (BaSO4) background. A UH5700 spectrophotometer with a 60 mm diameter integrating sphere measured data between 200 - 600 nm wavelength. Such data was then plotted using the Kubelka-Munk equation: \\u03b1/S = [(1\\u2212R)^2]/2R, with \\u03b1 being the absorption coefficient, S being the scattering coefficient, and R representing absolute reflectance.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2205,\n        \"id\": 507,\n        \"compound_name\": \"4-(R)-(+)-\\u03b2-methylphenethylammonium indium antimony chloride\",\n        \"formula\": \"C36H52N4In0.89Sb1.11Cl10\",\n        \"group\": \"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-\\u03b2-methylphenethylamine)4In2(1-x)Sb2xCl10\",\n        \"organic\": \"C9H13N\",\n        \"inorganic\": \"In0.89Sb1.11Cl10\",\n        \"iupac\": \"(R)-(+)-\\u03b2-methylphenethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"In2O3, MPA, HCl\",\n        \"synthesis_product\": \"Single crystals of 4-(R)-(+)-\\u03b2-methylphenethylamine indium antimony chloride\",\n        \"synthesis_description\": \"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 \\u03bcL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling.\",\n        \"experimental_method\": \"PL spectroscopy\",\n        \"experimental_description\": \"PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution). The excitation wavelength was 350 nm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2206,\n        \"id\": 507,\n        \"compound_name\": \"4-(R)-(+)-\\u03b2-methylphenethylammonium indium antimony chloride\",\n        \"formula\": \"C36H52N4In0.89Sb1.11Cl10\",\n        \"group\": \"(R-MPA)4In0.89Sb1.11Cl10, ((R)-(+)-\\u03b2-methylphenethylamine)4In2(1-x)Sb2xCl10\",\n        \"organic\": \"C9H13N\",\n        \"inorganic\": \"In0.89Sb1.11Cl10\",\n        \"iupac\": \"(R)-(+)-\\u03b2-methylphenethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"In2O3, MPA, HCl\",\n        \"synthesis_product\": \"Single crystals of 4-(R)-(+)-\\u03b2-methylphenethylamine indium antimony chloride\",\n        \"synthesis_description\": \"In2O3 (1 mmol, 0.292 g) and MPA (1 mmol, 146 \\u03bcL) were mixed together in an HCl solution (2 mL, 37%) and heated to 90 degrees Celsius. This solution was then cooled at a rate of 1 degree Celsius per hour. Single crystals of the material grew in the solution after about three days of such slowed cooling.\",\n        \"experimental_method\": \"PL spectroscopy\",\n        \"experimental_description\": \"PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution). For this material, the emission wavelength was 650 nm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2207,\n        \"id\": 509,\n        \"compound_name\": \"4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"formula\": \"C32H72N4In1.64Sb0.36Cl10\",\n        \"group\": \"(R-CHEA)4In1.64Sb0.36Cl10\",\n        \"organic\": \"C8H18N\",\n        \"inorganic\": \"In1.64Sb0.36Cl10\",\n        \"iupac\": \"(R)-(\\u2212)-1-cyclohexylethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"CHEA, In2O3, HCl\",\n        \"synthesis_product\": \"Single crystals of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"synthesis_description\": \"CHEA (1 mmol, 146 \\u03bcL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90\\u00b0Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1\\u00b0C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50\\u00b0C in a vacuum oven.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction (SC-XRD)\",\n        \"experimental_description\": \"SC-XRD data was collected via a Bruker D8 Venture diffractometer. Mo-K\\u03b1 radiation occurred at 173 K with \\u03bb = 0.71073 \\u00c5. Bruker APEX3, Olex2, and SHELXL software were used for further analysis.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2208,\n        \"id\": 509,\n        \"compound_name\": \"4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"formula\": \"C32H72N4In1.64Sb0.36Cl10\",\n        \"group\": \"(R-CHEA)4In1.64Sb0.36Cl10\",\n        \"organic\": \"C8H18N\",\n        \"inorganic\": \"In1.64Sb0.36Cl10\",\n        \"iupac\": \"(R)-(\\u2212)-1-cyclohexylethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"powder\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"CHEA, In2O3, HCl\",\n        \"synthesis_product\": \"Powder of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"synthesis_description\": \"CHEA (1 mmol, 146 \\u03bcL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90\\u00b0Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1\\u00b0C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50\\u00b0C in a vacuum oven. For UV-vis spectroscopy, these single crystals were then ground into a powder.\",\n        \"experimental_method\": \"UV-vis spectroscopy\",\n        \"experimental_description\": \"UV-vis spectroscopy was employed to record the absorbance of powder samples of the crystal, which were adhered onto a barium sulfate (BaSO4) background. A UH5700 spectrophotometer with a 60 mm diameter integrating sphere measured data between 200 - 600 nm wavelength. Such data was then plotted using the Kubelka-Munk equation: \\u03b1/S = [(1\\u2212R)^2]/2R, with \\u03b1 being the absorption coefficient, S being the scattering coefficient, and R representing absolute reflectance.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2209,\n        \"id\": 509,\n        \"compound_name\": \"4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"formula\": \"C32H72N4In1.64Sb0.36Cl10\",\n        \"group\": \"(R-CHEA)4In1.64Sb0.36Cl10\",\n        \"organic\": \"C8H18N\",\n        \"inorganic\": \"In1.64Sb0.36Cl10\",\n        \"iupac\": \"(R)-(\\u2212)-1-cyclohexylethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"photoluminescence excitation\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"CHEA, In2O3, HCl\",\n        \"synthesis_product\": \"Single crystals of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"synthesis_description\": \"CHEA (1 mmol, 146 \\u03bcL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90\\u00b0Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1\\u00b0C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50\\u00b0C in a vacuum oven.\",\n        \"experimental_method\": \"PL spectroscopy\",\n        \"experimental_description\": \"PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution). For this material, the emission wavelength was 710 nm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1002/anie.202215206\",\n        \"dataset_ID\": 2210,\n        \"id\": 509,\n        \"compound_name\": \"4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"formula\": \"C32H72N4In1.64Sb0.36Cl10\",\n        \"group\": \"(R-CHEA)4In1.64Sb0.36Cl10\",\n        \"organic\": \"C8H18N\",\n        \"inorganic\": \"In1.64Sb0.36Cl10\",\n        \"iupac\": \"(R)-(\\u2212)-1-cyclohexylethylaminium indium antimony chloride\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 0,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"arbitrary unit\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Turn-on Circularly Polarized Luminescence in Chiral Indium Chlorides by 5s2 Metal Centers\",\n        \"journal\": \"Angewandte Chemie\",\n        \"vol\": \"n/a\",\n        \"pages_start\": \"e202215206\",\n        \"pages_end\": \"e202215207\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"CHEA, In2O3, HCl\",\n        \"synthesis_product\": \"Single crystals of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride\",\n        \"synthesis_description\": \"CHEA (1 mmol, 146 \\u03bcL) and In2O3 (1 mmol, 0.292 g) were mixed together in a solution of HCl (37%, 2 mL). This solution was then heated up to 90\\u00b0Celsius and kept at this temperature until the materials dissolved. Then the solution was cooled at a rate of 1\\u00b0C per hour to room temperature, which took about three days and produced single crystals of 4-(R)-(\\u2212)-1-cyclohexylethylammonium indium antimony chloride. These crystals were cleaned and dried for 5 hours at 50\\u00b0C in a vacuum oven.\",\n        \"experimental_method\": \"PL spectroscopy\",\n        \"experimental_description\": \"PL measurements were recorded at room temperature on an Edinburgh FS5 spectrofluorometer utilizing xenon lamps as the source of excitation (1 nm resolution) at a 350 nm wavelength.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 2230,\n        \"id\": 510,\n        \"compound_name\": \"Multi-domain  PEA-modified Cesium Lead Bromide\",\n        \"formula\": \"(PEA)0.4-CsPbBr3\",\n        \"group\": \"\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CsPbBr3\",\n        \"iupac\": \"Cesium lead(II) bromide (multidomain) with 2-phenylethan-1-aminium additive\",\n        \"last_update\": \"2023-02-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Superfluorescence (SF) Spectra\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Room Temperature Superfluorescence in Hybrid Perovskites and Its Origins\",\n        \"journal\": \"Nature Photonics\",\n        \"vol\": \"16\",\n        \"pages_start\": \"324\",\n        \"pages_end\": \"329\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%)\",\n        \"synthesis_product\": \"Multi-domain  quasi-2D CsPbBr3 samples\",\n        \"synthesis_description\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%) were purchased from Sigma-Aldrich. Caesium bromide (CsBr, 99.999%) was purchased from Alfa Aesar. Further, (PEA)0.4CsPbBr3 precursors were prepared by dissolving PEABr, CsBr and PbBr2 in a molar ratio of 0.4:1.1:1.0 in 1\\u2009ml anhydrous dimethyl sulfoxide solvent to make 0.3\\u2009M (Pb2+ concentration) solutions. The solutions were stirred for 2\\u2009h at 60\\u2009\\u00b0C in a glovebox. The precursor solution was then spin coated on a glass substrate at 3,000\\u2009r.p.m. for 2\\u2009min, followed by annealing at 80\\u2009\\u00b0C for 10\\u2009min.\",\n        \"experimental_method\": \"Steady-state photoluminescence measurement.\",\n        \"experimental_description\": \"400\\u2009nm pulses obtained from a frequency-doubled Ti-sapphire amplifier (Quantronix Integra-C; repetition rate, 1\\u2009kHz; central wavelength, 800\\u2009nm) are used to excite the sample. Spectrometer from Mightex systems was used to measure the PL spectra emitted from the sample.\",\n        \"physical_property\": \"78.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 2231,\n        \"id\": 510,\n        \"compound_name\": \"Multi-domain  PEA-modified Cesium Lead Bromide\",\n        \"formula\": \"(PEA)0.4-CsPbBr3\",\n        \"group\": \"\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CsPbBr3\",\n        \"iupac\": \"Cesium lead(II) bromide (multidomain) with 2-phenylethan-1-aminium additive\",\n        \"last_update\": \"2023-02-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Superfluorescence (SF)\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Room Temperature Superfluorescence in Hybrid Perovskites and Its Origins\",\n        \"journal\": \"Nature Photonics\",\n        \"vol\": \"16\",\n        \"pages_start\": \"324\",\n        \"pages_end\": \"329\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 2232,\n        \"id\": 510,\n        \"compound_name\": \"Multi-domain  PEA-modified Cesium Lead Bromide\",\n        \"formula\": \"(PEA)0.4-CsPbBr3\",\n        \"group\": \"\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CsPbBr3\",\n        \"iupac\": \"Cesium lead(II) bromide (multidomain) with 2-phenylethan-1-aminium additive\",\n        \"last_update\": \"2023-02-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Superfluorescence (SF) Spectra\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Room Temperature Superfluorescence in Hybrid Perovskites and Its Origins\",\n        \"journal\": \"Nature Photonics\",\n        \"vol\": \"16\",\n        \"pages_start\": \"324\",\n        \"pages_end\": \"329\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%)\",\n        \"synthesis_product\": \"Multi-domain quasi-2D CsPbBr3 samples\",\n        \"synthesis_description\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%) were purchased from Sigma-Aldrich. Caesium bromide (CsBr, 99.999%) was purchased from Alfa Aesar. Further, (PEA)0.4CsPbBr3 precursors were prepared by dissolving PEABr, CsBr and PbBr2 in a molar ratio of 0.4:1.1:1.0 in 1\\u2009ml anhydrous dimethyl sulfoxide solvent to make 0.3\\u2009M (Pb2+ concentration) solutions. The solutions were stirred for 2\\u2009h at 60\\u2009\\u00b0C in a glovebox. The precursor solution was then spin coated on a glass substrate at 3,000\\u2009r.p.m. for 2\\u2009min, followed by annealing at 80\\u2009\\u00b0C for 10\\u2009min.\",\n        \"experimental_method\": \"Steady-state photoluminescence measurement.\",\n        \"experimental_description\": \"400\\u2009nm pulses obtained from a frequency-doubled Ti-sapphire amplifier (Quantronix Integra-C; repetition rate, 1\\u2009kHz; central wavelength, 800\\u2009nm) are used to excite the sample. Spectrometer from Mightex systems was used to measure the PL spectra emitted from the sample.\",\n        \"physical_property\": \"300.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 2233,\n        \"id\": 510,\n        \"compound_name\": \"Multi-domain  PEA-modified Cesium Lead Bromide\",\n        \"formula\": \"(PEA)0.4-CsPbBr3\",\n        \"group\": \"\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CsPbBr3\",\n        \"iupac\": \"Cesium lead(II) bromide (multidomain) with 2-phenylethan-1-aminium additive\",\n        \"last_update\": \"2023-02-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Superfluorescence (SF) Time-resolved PL\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"time\",\n        \"secondary_unit\": \"ps\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Room Temperature Superfluorescence in Hybrid Perovskites and Its Origins\",\n        \"journal\": \"Nature Photonics\",\n        \"vol\": \"16\",\n        \"pages_start\": \"324\",\n        \"pages_end\": \"329\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%)\",\n        \"synthesis_product\": \"Multi-domain quasi-2D CsPbBr3 samples\",\n        \"synthesis_description\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%) were purchased from Sigma-Aldrich. Caesium bromide (CsBr, 99.999%) was purchased from Alfa Aesar. Further, (PEA)0.4CsPbBr3 precursors were prepared by dissolving PEABr, CsBr and PbBr2 in a molar ratio of 0.4:1.1:1.0 in 1\\u2009ml anhydrous dimethyl sulfoxide solvent to make 0.3\\u2009M (Pb2+ concentration) solutions. The solutions were stirred for 2\\u2009h at 60\\u2009\\u00b0C in a glovebox. The precursor solution was then spin coated on a glass substrate at 3,000\\u2009r.p.m. for 2\\u2009min, followed by annealing at 80\\u2009\\u00b0C for 10\\u2009min.\",\n        \"experimental_method\": \"Time resolved Kerr-gate experiment\",\n        \"experimental_description\": \"Time-resolved SF was measured with a home-built Kerr-gate set-up using a 1-kHz amplified Ti:sapphire laser (Quantronix Integra-C) with 120-fs pulsed output at 800\\u2009nm. The laser output beam was split into two paths, one for the optical Kerr-gate pulse and the other for the excitation beam, which was converted to 400\\u2009nm through second harmonic generation using a beta barium borate crystal. The collected PL and the gate pulse were focused on CS2 in a 2-mm-thick cuvette, which was used as the Kerr medium. The gated signal was measured with a Hamamatsu photomultiplier tube (H10721-20) attached to a monochromator. The sample was kept in a Janis continuous-flow liquid-nitrogen cryostat. The excitation beam size was 1.5\\u2009mm.\",\n        \"physical_property\": \"4.4\",\n        \"unit\": \"uJ/cm2\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 2234,\n        \"id\": 510,\n        \"compound_name\": \"Multi-domain  PEA-modified Cesium Lead Bromide\",\n        \"formula\": \"(PEA)0.4-CsPbBr3\",\n        \"group\": \"\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CsPbBr3\",\n        \"iupac\": \"Cesium lead(II) bromide (multidomain) with 2-phenylethan-1-aminium additive\",\n        \"last_update\": \"2023-02-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Superfluorescence (SF) Time-resolved PL\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"time\",\n        \"secondary_unit\": \"ps\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Room Temperature Superfluorescence in Hybrid Perovskites and Its Origins\",\n        \"journal\": \"Nature Photonics\",\n        \"vol\": \"16\",\n        \"pages_start\": \"324\",\n        \"pages_end\": \"329\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%)\",\n        \"synthesis_product\": \"Multi-domain quasi-2D CsPbBr3 samples\",\n        \"synthesis_description\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%) were purchased from Sigma-Aldrich. Caesium bromide (CsBr, 99.999%) was purchased from Alfa Aesar. Further, (PEA)0.4CsPbBr3 precursors were prepared by dissolving PEABr, CsBr and PbBr2 in a molar ratio of 0.4:1.1:1.0 in 1\\u2009ml anhydrous dimethyl sulfoxide solvent to make 0.3\\u2009M (Pb2+ concentration) solutions. The solutions were stirred for 2\\u2009h at 60\\u2009\\u00b0C in a glovebox. The precursor solution was then spin coated on a glass substrate at 3,000\\u2009r.p.m. for 2\\u2009min, followed by annealing at 80\\u2009\\u00b0C for 10\\u2009min.\",\n        \"experimental_method\": \"Time resolved Kerr-gate experiment\",\n        \"experimental_description\": \"Time-resolved SF was measured with a home-built Kerr-gate set-up using a 1-kHz amplified Ti:sapphire laser (Quantronix Integra-C) with 120-fs pulsed output at 800\\u2009nm. The laser output beam was split into two paths, one for the optical Kerr-gate pulse and the other for the excitation beam, which was converted to 400\\u2009nm through second harmonic generation using a beta barium borate crystal. The collected PL and the gate pulse were focused on CS2 in a 2-mm-thick cuvette, which was used as the Kerr medium. The gated signal was measured with a Hamamatsu photomultiplier tube (H10721-20) attached to a monochromator. The sample was kept in a Janis continuous-flow liquid-nitrogen cryostat. The excitation beam size was 1.5\\u2009mm.\",\n        \"physical_property\": \"16.8\",\n        \"unit\": \"uJ/cm2\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"\",\n        \"dataset_ID\": 2235,\n        \"id\": 510,\n        \"compound_name\": \"Multi-domain  PEA-modified Cesium Lead Bromide\",\n        \"formula\": \"(PEA)0.4-CsPbBr3\",\n        \"group\": \"\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CsPbBr3\",\n        \"iupac\": \"Cesium lead(II) bromide (multidomain) with 2-phenylethan-1-aminium additive\",\n        \"last_update\": \"2023-02-21\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Superfluorescence (SF) Phase Diagram\",\n        \"primary_unit\": \"K\",\n        \"secondary_name\": \"Fluence\",\n        \"secondary_unit\": \"uJ/cm2\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Room Temperature Superfluorescence in Hybrid Perovskites and Its Origins\",\n        \"journal\": \"Nature Photonics\",\n        \"vol\": \"16\",\n        \"pages_start\": \"324\",\n        \"pages_end\": \"329\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%)\",\n        \"synthesis_product\": \"Multi-domain quasi-2D CsPbBr3 samples\",\n        \"synthesis_description\": \"Lead bromide (PbBr2, 99.999%), phenethylammonium bromide (PEABr, \\u226598%) and dimethyl sulfoxide (anhydrous, 99.9%) were purchased from Sigma-Aldrich. Caesium bromide (CsBr, 99.999%) was purchased from Alfa Aesar. Further, (PEA)0.4CsPbBr3 precursors were prepared by dissolving PEABr, CsBr and PbBr2 in a molar ratio of 0.4:1.1:1.0 in 1\\u2009ml anhydrous dimethyl sulfoxide solvent to make 0.3\\u2009M (Pb2+ concentration) solutions. The solutions were stirred for 2\\u2009h at 60\\u2009\\u00b0C in a glovebox. The precursor solution was then spin coated on a glass substrate at 3,000\\u2009r.p.m. for 2\\u2009min, followed by annealing at 80\\u2009\\u00b0C for 10\\u2009min.\",\n        \"experimental_method\": \"Time resolved Kerr-gate experiment\",\n        \"experimental_description\": \"Time-resolved SF was measured with a home-built Kerr-gate set-up using a 1-kHz amplified Ti:sapphire laser (Quantronix Integra-C) with 120-fs pulsed output at 800\\u2009nm. The laser output beam was split into two paths, one for the optical Kerr-gate pulse and the other for the excitation beam, which was converted to 400\\u2009nm through second harmonic generation using a beta barium borate crystal. The collected PL and the gate pulse were focused on CS2 in a 2-mm-thick cuvette, which was used as the Kerr medium. The gated signal was measured with a Hamamatsu photomultiplier tube (H10721-20) attached to a monochromator. The sample was kept in a Janis continuous-flow liquid-nitrogen cryostat. The excitation beam size was 1.5\\u2009mm.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2236,\n        \"id\": 516,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~17.3 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~17.3 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2237,\n        \"id\": 517,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~7.9 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~7.9 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2238,\n        \"id\": 518,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~7.4 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~7.4 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2239,\n        \"id\": 519,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~6.9 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~6.9 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2240,\n        \"id\": 520,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~6.2 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~6.2 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2241,\n        \"id\": 521,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~5.4 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~5.4 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2242,\n        \"id\": 522,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~4.9 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~4.9 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorbance\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2243,\n        \"id\": 516,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~17.3 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~17.3 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2244,\n        \"id\": 517,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~7.9 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~7.9 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2245,\n        \"id\": 518,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~7.4 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~7.4 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2246,\n        \"id\": 519,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~6.9 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~6.9 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2247,\n        \"id\": 520,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~6.2 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~6.2 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2248,\n        \"id\": 521,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~5.4 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~5.4 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"doi.org/10.1038/s41563-022-01349-4\",\n        \"dataset_ID\": 2249,\n        \"id\": 522,\n        \"compound_name\": \"Oleylammonium capped cesium lead iodide quantum dots (~4.9 nm)\",\n        \"formula\": \"C18H37N-CsPbI3\",\n        \"group\": \"Cesium lead iodide, Cesium lead iodide with oleylamine\",\n        \"organic\": \"C18H37N\",\n        \"inorganic\": \"CsPbI3\",\n        \"iupac\": \"cesium lead(II) iodide with (9Z)-octadec-9-en-1-aminium\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"quantum dots of size ~4.9 nm\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"\",\n        \"derived_to_from\": [\n            38\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"PL intensity\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Lattice distortion inducing exciton splitting and coherent quantum beating in CsPbI3 perovskite quantum dots\",\n        \"journal\": \"Nature Materials\",\n        \"vol\": \"21\",\n        \"pages_start\": \"1282\",\n        \"pages_end\": \"1289\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"Cs2CO3, PbI2, ZnI2, oleic acid (OA), 1-octadecene (ODE), oleylamine (OAm), bis(2,4,4-trimethylpentyl) phosphinic acid (TMPPA), methyl acetate, hexane\",\n        \"synthesis_product\": \"CsPbI3 quantum dots\",\n        \"synthesis_description\": \"A hot-injection approach was used to synthesize cesium lead iodide quantum dots. Cs2CO3 (0.25g, 99.9%), OA (0.98 mL, 90%), and ODE (9 mL, 90%) were mixed in a 25 mL three-neck flask and vacuum dried at 120 degrees Celsius for one hour through the use of a Schlenk line. Cs2CO3 was dissolved by heating the solution to 150 degrees C for 10 minutes, and this initial solution was then kept at 100 degrees C to prevent precipitation. \\r\\nPbI2 (120 mg, 99.99%) and ZnI2 (250 mg, 99.99%) were dissolved in a blend of ODE (5 mL), OAm (2 mL), and TMPPA (2 mL) at 120 degrees C for one hour. This solution was then set to a reaction temperature dependent upon the desired QD size (between 145 and 190\\u00b0C). \\r\\nThe initial solution (0.4 mL) was injected into the second solution, and after 20 seconds the flask was quenched in an ice bath. To separate QDs from unreacted salts, the product was centrifuged for 30 minutes at 1,290 g. QDs were collected and, after methyl acetate was used to isolate the QDs, they were suspended in hexane.\",\n        \"experimental_method\": \"Pump-pulse spectroscopy\",\n        \"experimental_description\": \"QD films were spin-coated onto glass substrates (2000 rpm, 40 seconds) and mounted to a liquid nitrogen cooling system for this experiment. A 1030 nm laser was split into two beams (80% and 20%). The 80% beam pumped an Orpheus-HP optical parameter amplifier and generated a tunable pump beam, while the 20% was split again into two parts (75% and 25%). The 75% beam was focused into a 13-mm yttrium aluminum garnet crystal in order to create a white light probe beam. This probe beam was focused onto the sample with a parabolic reflector, then into a fibre-coupled spectrometer (10 kHz frequency). Pump pulses were chopped at 5 kHz before absorbance change was calculated with 10 pump-blocked pulses and 10 pump-unblocked pulses.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"manual extraction\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acsnano.1c01134\",\n        \"dataset_ID\": 2250,\n        \"id\": 511,\n        \"compound_name\": \"Bis(R-)methylbenzylammonium copper chloride\",\n        \"formula\": \"C16N2H242CuCl4\",\n        \"group\": \"R-MBA2CuCl4\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CuCl4\",\n        \"iupac\": \"bis(R-)methylbenzylaminium copper (II) chloride\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Direct Detection of Circularly Polarized Light Using Chiral Copper Chloride\\u2013Carbon Nanotube Heterostructures\",\n        \"journal\": \"American Chemical Society\",\n        \"vol\": \"15\",\n        \"pages_start\": \"7608\",\n        \"pages_end\": \"7617\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(R)-(+)-\\u03b1-methylbenzylamine (R-MBA), ethanol, HCl, diethyl ether, copper(II) chloride dihydrate\",\n        \"synthesis_product\": \"Single crystals of Bis(R-)methylbenzylammonium copper chloride\",\n        \"synthesis_description\": \"The synthesis of a precursor solution, MBACl, was done by adding R-MBA (5 mL) and ethanol (15 mL) to a round-bottom flask (250 mL), and stirring the mixture at 0 degrees Celsius. HCl (10 mL, 37%) was added, and the solution was stirred for two hours. Then, copper(II) chloride dihydrate (171 mg, 1 mmol), MBACl (315 mg, 2 mmol), and isopropyl alcohol were added to a vial under heat and stirred until all solids dissolved. The resulting dark green solution cooled to room temperature, while green single crystals of Bis(R-)methylbenzylammonium copper chloride were precipitated. Crystals were washed by diethyl ether and vacuum-dried.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal structure data was collected using a Bruker KAPPA APEX II diffractometer, APEX II CCD detector, and a Mo K\\u03b1 source (\\u03bb = 0.71073 \\u00c5). APEX and Olex2 software was used for further refinement.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acsnano.1c01134\",\n        \"dataset_ID\": 2251,\n        \"id\": 512,\n        \"compound_name\": \"Bis(S-)methylbenzylammonium copper chloride\",\n        \"formula\": \"C16N2H242CuCl4\",\n        \"group\": \"S-MBA2CuCl4\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CuCl4\",\n        \"iupac\": \"bis(S-)methylbenzylaminium copper (II) chloride\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Direct Detection of Circularly Polarized Light Using Chiral Copper Chloride\\u2013Carbon Nanotube Heterostructures\",\n        \"journal\": \"American Chemical Society\",\n        \"vol\": \"15\",\n        \"pages_start\": \"7608\",\n        \"pages_end\": \"7617\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(S)-(\\u2212)-\\u03b1-methylbenzylamine (S-MBA), ethanol, HCl, diethyl ether, copper(II) chloride dihydrate\",\n        \"synthesis_product\": \"Single crystals of Bis(S-)methylbenzylammonium copper chloride\",\n        \"synthesis_description\": \"The synthesis of a precursor solution, MBACl, was done by adding S-MBA (5 mL) and ethanol (15 mL) to a round-bottom flask (250 mL), and stirring the mixture at 0 degrees Celsius. HCl (10 mL, 37%) was added, and the solution was stirred for two hours. Then, copper(II) chloride dihydrate (171 mg, 1 mmol), MBACl (315 mg, 2 mmol), and isopropyl alcohol were added to a vial under heat and stirred until all solids dissolved. The resulting dark green solution cooled to room temperature, while green single crystals of Bis(S-)methylbenzylammonium copper chloride were precipitated. Crystals were washed by diethyl ether and vacuum-dried.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal structure data was collected using a Bruker KAPPA APEX II diffractometer, APEX II CCD detector, and a Mo K\\u03b1 source (\\u03bb = 0.71073 \\u00c5). APEX and Olex2 software was used for further refinement.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c03492\",\n        \"dataset_ID\": 2254,\n        \"id\": 292,\n        \"compound_name\": \"Bis(3-iodopropylammonium) lead iodide\",\n        \"formula\": \"C6H18N2PbI6\",\n        \"group\": \"(I(CH2)3NH3)2PbI4, bis(3-iodopropylaminium) tetraiodoplumbate(II), Bis(PIA)PbI4, (IPA)2PbI4\",\n        \"organic\": \"C3H9NI\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(3-iodopropylaminium) lead (II) iodide\",\n        \"last_update\": \"2023-02-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Absorption (Kubelka\\u2212Munk)\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Iodine\\u2212Iodine Interactions Suppressing Phase Transitions of 2D Layered Hybrid (I-(CH2)n\\u2010NH3)2PbI4 (n = 2\\u22126) Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"288\",\n        \"pages_end\": \"296\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"PbO, HI (57% (w/w) in water), H3PO2 (50% (w/w) in water)\",\n        \"synthesis_product\": \"yellow plate-like crystals\",\n        \"synthesis_description\": \"5 mmol PbO was dissolved in a solution of 40 mL HI and 5 mL of H3PO2 by sonicating in an ultrasonic bath sonicator for 10 min. The solution is cooled to \\u223c278 K using an ice\\u2212water bath. In this solution, 10 mmol H2N-(CH2)3-OH is added dropwise. The solution is stirred using a magnetic stirrer and heated for 30 min in an oil bath maintained at 383 K.  After 30 min, the heating and stirring are stopped, and the solution is kept undisturbed. After 12 hours, the precipitated crystals are separated by filtration with diethyl ether and dried in air.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"The spectrum was recorded using a Shimadzu UV3600 plus UV\\u2212vis\\u2212NIR spectrophotometer with BaSO4 powder as a reference of 100% reflectance. The reflectance signal is converted to absorbance using the Kubelka\\u2212Munk function.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"monoclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/acs.chemmater.1c03492\",\n        \"dataset_ID\": 2255,\n        \"id\": 387,\n        \"compound_name\": \"Ruddlesden-Popper\",\n        \"formula\": \"(RNH3)2(A)n\\u22121MX3n+1\",\n        \"group\": \"*\",\n        \"organic\": \"N/A\",\n        \"inorganic\": \"(A)n\\u22121MX3n+1\",\n        \"iupac\": \"\",\n        \"last_update\": \"2021-08-24\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"Absorption (Kubelka\\u2212Munk)\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Iodine\\u2212Iodine Interactions Suppressing Phase Transitions of 2D Layered Hybrid (I-(CH2)n\\u2010NH3)2PbI4 (n = 2\\u22126) Perovskites\",\n        \"journal\": \"Chemistry of Materials\",\n        \"vol\": \"34\",\n        \"pages_start\": \"288\",\n        \"pages_end\": \"296\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"PbO, HI (57% (w/w) in water), H3PO2 (50% (w/w) in water)\",\n        \"synthesis_product\": \"yellow plate-like crystals\",\n        \"synthesis_description\": \"5 mmol PbO was dissolved in a solution of 40 mL HI and 5 mL of H3PO2 by sonicating in an ultrasonic bath sonicator for 10 min. The solution is cooled to \\u223c278 K using an ice\\u2212water bath. In this solution, 10 mmol H2N-(CH2)3-OH is added dropwise. The solution is stirred using a magnetic stirrer and heated for 30 min in an oil bath maintained at 383 K.  After 30 min, the heating and stirring are stopped, and the solution is kept undisturbed. After 12 hours, the precipitated crystals are separated by filtration with diethyl ether and dried in air.\",\n        \"experimental_method\": \"Diffuse reflectance spectroscopy\",\n        \"experimental_description\": \"The spectrum was recorded using a Shimadzu UV3600 plus UV\\u2212vis\\u2212NIR spectrophotometer with BaSO4 powder as a reference of 100% reflectance. The reflectance signal is converted to absorbance using the Kubelka\\u2212Munk function.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.2c12034\",\n        \"dataset_ID\": 2256,\n        \"id\": 514,\n        \"compound_name\": \"N-methyl 3-iodopropylammonium lead iodide\",\n        \"formula\": \"C8N2H22PbI6\",\n        \"group\": \"(MIPA)2PbI4\",\n        \"organic\": \"C4H11NI\",\n        \"inorganic\": \"PbI4\",\n        \"iupac\": \"bis(3-iodo-N-methylpropan-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2023-04-19\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Rational Design of Non-Centrosymmetric Hybrid Halide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"145\",\n        \"pages_start\": \"1378\",\n        \"pages_end\": \"1388\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"Lead oxide (Sigma Aldrich, PbO, 99.9%), hydroiodic acid (Sigma Aldrich, HI, 57% w/w in water), hypophosphorous acid (Avra chemicals, H3PO2, 50% w/w in water), 3-methylamino 1-propanol (Sigma Aldrich, HO-(CH2)3-N(CH3)H, 96%)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"2.5 mmol of PbO was dissolved in a mixture of 20 mL HI and 3 mL H3PO2 in a glass beaker at room temperature using sonication for 10 minutes in an ultrasonic bath sonicator. To this, 5 mmol of OH-(CH2)3- NH(CH3) (for MIPA) was added dropwise. The mixture was heated and stirred at 110 oC for 30 minutes using an oil bath placed on a heater and magnetic stirrer. After 30 minutes, the heating and stirring were stopped, and the clear yellow solution was allowed to cool undisturbed to room temperature. After 24 hours, the precipitated crystals were collected using suction filtration, washed with diethyl ether, and dried in the air.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Data were collected in a Bruker Apex Duo diffractometer using Mo K\\u03b1 radiation (\\u03bb = 0.71 \\u00c5). The integrations of the collected data and numerical absorption corrections were done using APEX3 software. The structures were solved by the direct method using SHELXS and refined by full-matrix least-squares on F2 using the SHELXL, as implemented in Olex2.\",\n        \"physical_property\": \"100.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"Aba2\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"10.1021/jacs.2c12034\",\n        \"dataset_ID\": 2257,\n        \"id\": 514,\n        \"compound_name\": \"N-methyl 3-iodopropylammonium lead iodide\",\n        \"formula\": \"C8N2H22PbI6\",\n        \"group\": \"(MIPA)2PbI4\",\n        \"organic\": \"C4H11NI\",\n        \"inorganic\": \"PbI4\",\n        \"iupac\": \"bis(3-iodo-N-methylpropan-1-aminium) lead (II) iodide\",\n        \"last_update\": \"2023-04-19\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"\\u03b1/S\",\n        \"secondary_name\": \"Energy\",\n        \"secondary_unit\": \"eV\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Rational Design of Non-Centrosymmetric Hybrid Halide Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"145\",\n        \"pages_start\": \"1378\",\n        \"pages_end\": \"1388\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"Lead oxide (Sigma Aldrich, PbO, 99.9%), hydroiodic acid (Sigma Aldrich, HI, 57% w/w in water), hypophosphorous acid (Avra chemicals, H3PO2, 50% w/w in water), 3-methylamino 1-propanol (Sigma Aldrich, HO-(CH2)3-N(CH3)H, 96%)\",\n        \"synthesis_product\": \"Orange plate-like crystals\",\n        \"synthesis_description\": \"2.5 mmol of PbO was dissolved in a mixture of 20 mL HI and 3 mL H3PO2 in a glass beaker at room temperature using sonication for 10 minutes in an ultrasonic bath sonicator. To this, 5 mmol of OH-(CH2)3- NH(CH3) (for MIPA) was added dropwise. The mixture was heated and stirred at 110 oC for 30 minutes using an oil bath placed on a heater and magnetic stirrer. After 30 minutes, the heating and stirring were stopped, and the clear yellow solution was allowed to cool undisturbed to room temperature. After 24 hours, the precipitated crystals were collected using suction filtration, washed with diethyl ether, and dried in the air.\",\n        \"experimental_method\": \"Diffuse reflectance\",\n        \"experimental_description\": \"The spectrum was recorded using a Shimadzu UV3600 plus UV\\u2212vis\\u2212NIR spectrophotometer with BaSO4 powder as a reference of 100% reflectance. The reflectance signal is converted to absorbance using the Kubelka\\u2212Munk function.\",\n        \"physical_property\": \"298.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"orthorhombic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"From author\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/acsnano.1c01134\",\n        \"dataset_ID\": 2258,\n        \"id\": 515,\n        \"compound_name\": \"Bis(rac-)methylbenzylammonium copper chloride\",\n        \"formula\": \"C16N2H242CuCl4\",\n        \"group\": \"rac-MBA2CuCl4, (racemic-MBA)2CuCl4\",\n        \"organic\": \"C8NH12\",\n        \"inorganic\": \"CuCl4\",\n        \"iupac\": \"bis(rac-)methylbenzylaminium copper (II) chloride\",\n        \"last_update\": \"2023-03-07\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Direct Detection of Circularly Polarized Light Using Chiral Copper Chloride\\u2013Carbon Nanotube Heterostructures\",\n        \"journal\": \"American Chemical Society\",\n        \"vol\": \"15\",\n        \"pages_start\": \"7608\",\n        \"pages_end\": \"7617\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"(\\u00b1)-\\u03b1-methylbenzylamine (rac-MBA), ethanol, HCl, diethyl ether, copper(II) chloride dihydrate\",\n        \"synthesis_product\": \"Single crystals of Bis(rac-)methylbenzylammonium copper chloride\",\n        \"synthesis_description\": \"The synthesis of a precursor solution, MBACl, was done by adding rac-MBA (5 mL) and ethanol (15 mL) to a round-bottom flask (250 mL), and stirring the mixture at 0 degrees Celsius. HCl (10 mL, 37%) was added, and the solution was stirred for two hours. Then, copper(II) chloride dihydrate (171 mg, 1 mmol), MBACl (315 mg, 2 mmol), and isopropyl alcohol were added to a vial under heat and stirred until all solids dissolved. The resulting dark green solution cooled to room temperature, while green single crystals of Bis(rac-)methylbenzylammonium copper chloride were precipitated. Crystals were washed by diethyl ether and vacuum-dried.\",\n        \"experimental_method\": \"Single-crystal X-ray diffraction\",\n        \"experimental_description\": \"Single-crystal structure data was collected using a Bruker KAPPA APEX II diffractometer, APEX II CCD detector, and a Mo K\\u03b1 source (\\u03bb = 0.71073 \\u00c5). APEX and Olex2 software was used for further refinement.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/d1nr06899g\",\n        \"dataset_ID\": 2259,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2260,\n            2261,\n            2266\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"On the optical anisotropy in 2D metal-halide perovskites\",\n        \"journal\": \"Nanoscale\",\n        \"vol\": \"14\",\n        \"pages_start\": \"752\",\n        \"pages_end\": \"765\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",\n        \"synthesis_product\": \"Exfoliated single crystal flakes of (PEA)2PbI4.\",\n        \"synthesis_description\": \"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 \\u00b0C. The solution is then slowly cooled to room temperature at a rate of 2 \\u00b0C h\\u22121, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",\n        \"experimental_method\": \"Reflection mode and transmission mode ellipsometry\",\n        \"experimental_description\": \"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45\\u00b0 to 75\\u00b0 using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from \\u221210\\u00b0 to 70\\u00b0. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"from publication by author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/d1nr06899g\",\n        \"dataset_ID\": 2260,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2259,\n            2261,\n            2266\n        ],\n        \"primary_name\": \"exciton binding energy\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"On the optical anisotropy in 2D metal-halide perovskites\",\n        \"journal\": \"Nanoscale\",\n        \"vol\": \"14\",\n        \"pages_start\": \"752\",\n        \"pages_end\": \"765\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",\n        \"synthesis_product\": \"Exfoliated single crystal flakes of (PEA)2PbI4.\",\n        \"synthesis_description\": \"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 \\u00b0C. The solution is then slowly cooled to room temperature at a rate of 2 \\u00b0C h\\u22121, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",\n        \"experimental_method\": \"Reflection mode and transmission mode ellipsometry\",\n        \"experimental_description\": \"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45\\u00b0 to 75\\u00b0 using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from \\u221210\\u00b0 to 70\\u00b0. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"from publication by author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/d1nr06899g\",\n        \"dataset_ID\": 2261,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2259,\n            2260,\n            2266\n        ],\n        \"primary_name\": \"Exciton energy\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"On the optical anisotropy in 2D metal-halide perovskites\",\n        \"journal\": \"Nanoscale\",\n        \"vol\": \"14\",\n        \"pages_start\": \"752\",\n        \"pages_end\": \"765\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",\n        \"synthesis_product\": \"Exfoliated single crystal flakes of (PEA)2PbI4.\",\n        \"synthesis_description\": \"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 \\u00b0C. The solution is then slowly cooled to room temperature at a rate of 2 \\u00b0C h\\u22121, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",\n        \"experimental_method\": \"Reflection mode and transmission mode ellipsometry\",\n        \"experimental_description\": \"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45\\u00b0 to 75\\u00b0 using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from \\u221210\\u00b0 to 70\\u00b0. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"from publication by author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/d1nr06899g\",\n        \"dataset_ID\": 2266,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 3,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            2259,\n            2260,\n            2261\n        ],\n        \"primary_name\": \"Exciton energy\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"On the optical anisotropy in 2D metal-halide perovskites\",\n        \"journal\": \"Nanoscale\",\n        \"vol\": \"14\",\n        \"pages_start\": \"752\",\n        \"pages_end\": \"765\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethylammonium, fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution.\",\n        \"synthesis_product\": \"Exfoliated single crystal flakes of (PEA)2PbI4.\",\n        \"synthesis_description\": \"2D perovskite PEPI single crystals are synthesized based on previously reported slow-cooling method in Ref. https://dx.doi.org/10.1021/acsenergylett.8b01315. 200 mg (0.90 mmol) of PbO and 200 \\u03bcL (1.59 mmol) of phenylethyl- ammonium are fully dissolved in 4 mL of HI and 0.5 mL of H3PO2 solution at 90 \\u00b0C. The solution is then slowly cooled to room temperature at a rate of 2 \\u00b0C h\\u22121, giving orange sheet-like crystals. The crystals are then isolated from the parent solution by vacuum filtration, washed by a small amount of diethyl ether, and dried under vacuum. Thin crystals were exfoliated from the parent crystal using stiff heat release tape that serves as a handle. Sequential exfoliation steps with the tape yield successively thinner crystals. Many crystals were surveyed to select the best surface quality, flatness, and area.\",\n        \"experimental_method\": \"Reflection mode and transmission mode ellipsometry\",\n        \"experimental_description\": \"Transmittance was collected on a Cary 7000 UV-VIS-NIR spectrophotometer. Reflection ellipsometry was collected on a JA Woollam M2000DI at 45\\u00b0 to 75\\u00b0 using tape to suppress backside reflections. Transmission ellipsometry was collected on a JA Woollam M2000DI from \\u221210\\u00b0 to 70\\u00b0. The three data sets were processed as a multisample analysis in CompleteEASE. For bulk and cleaved crystals, reflection ellipsometry and reflection Mueller Matrix were collected using focus probes and either a JA Woollam M2000 or RC2, respectively.\",\n        \"physical_property\": \"293.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"P-1\",\n        \"extraction_method\": \"from publication by author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/d1nr06899g\",\n        \"dataset_ID\": 2267,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            225,\n            745,\n            1901,\n            1903,\n            2269\n        ],\n        \"primary_name\": \"band gap (fundamental)\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": false,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Spin-orbit coupled hybrid DFT\",\n        \"xc_functional\": \"HSE06 functional; exchange mixing parameter: 0.25, screening parameter: 0.11 (Bohr radii)^(-1)\",\n        \"k_point_grid\": \"3x7x7\",\n        \"level_of_relativity\": \"Spin-orbit coupling included as follows: Self-consistent scalar relativity (atomic zero-order regular approximation) with spin-orbit coupling applied non-selfconsistently in the energy band structure calculation.\",\n        \"basis_set_definition\": \"All-electron; \\\"intermediate\\\" numerical settings and basis sets.\",\n        \"numerical_accuracy\": \"Note that DFT-computed energy band gap values, even at the level of DFT-HS06+SOC, are not intended to capture the experimentally correct fundamental gap with quantitative accuracy. Rather, they are collected be comparable to other computational band gaps at the same level of theory in order to capture trends between different sources.\",\n        \"title\": \"On the optical anisotropy in 2D metal-halide perovskites\",\n        \"journal\": \"Nanoscale\",\n        \"vol\": \"14\",\n        \"pages_start\": \"752\",\n        \"pages_end\": \"765\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from publication by author\"\n    },\n    {\n        \"doi_isbn\": \"10.1039/d1nr06899g\",\n        \"dataset_ID\": 2269,\n        \"id\": 9,\n        \"compound_name\": \"Bis(phenylethylammonium) lead iodide\",\n        \"formula\": \"C16H24N2PbI4\",\n        \"group\": \"bis(2-phenylethane-1-aminium) tetraiodoplumbate(II), Bisphenylethylammonium lead iodide, phenethylammonium lead iodide, (PEA)2PbI4, PEA2PbI4, (C6H5C2H4NH3)2PbI4, (C8H12N)2PbI4, (C8H9NH3)2PbI4, PEA lead iodide, (PEA)2 lead iodide\",\n        \"organic\": \"C8H12N\",\n        \"inorganic\": \"PbI4, Lead iodide\",\n        \"iupac\": \"bis(2-phenylethane-1-aminium) lead(II) iodide\",\n        \"last_update\": \"2023-01-31\",\n        \"description\": \"Parallel organics\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"1\",\n        \"derived_to_from\": [\n            473,\n            488\n        ],\n        \"tags\": [],\n        \"Related_data_setID\": [\n            225,\n            745,\n            1901,\n            1903,\n            2267\n        ],\n        \"primary_name\": \"band structure\",\n        \"primary_unit\": \"eV\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": true,\n        \"is_experimental\": false,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"FHI-aims\",\n        \"level_of_theory\": \"Spin-orbit coupled hybrid DFT\",\n        \"xc_functional\": \"HSE06 functional; exchange mixing parameter: 0.25, screening parameter: 0.11 (Bohr radii)^(-1)\",\n        \"k_point_grid\": \"3x7x7\",\n        \"level_of_relativity\": \"Spin-orbit coupling included as follows: Self-consistent scalar relativity (atomic zero-order regular approximation) with spin-orbit coupling applied non-selfconsistently in the energy band structure calculation.\",\n        \"basis_set_definition\": \"All-electron; \\\"intermediate\\\" numerical settings and basis sets.\",\n        \"numerical_accuracy\": \"Note that DFT-computed energy band gap values, even at the level of DFT-HS06+SOC, are not intended to capture the experimentally correct fundamental gap with quantitative accuracy. Rather, they are collected be comparable to other computational band gaps at the same level of theory in order to capture trends between different sources.\",\n        \"title\": \"On the optical anisotropy in 2D metal-halide perovskites\",\n        \"journal\": \"Nanoscale\",\n        \"vol\": \"14\",\n        \"pages_start\": \"752\",\n        \"pages_end\": \"765\",\n        \"year\": \"2022\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"triclinic\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"from publication by author\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.1c06841\",\n        \"dataset_ID\": 2270,\n        \"id\": 523,\n        \"compound_name\": \"S-\\u03b2-methylphenethylammonium butylammonium lead bromide\",\n        \"formula\": \"C13H25N2PbBr4\",\n        \"group\": \"[S-MePEA][C3A]PbBr4\",\n        \"organic\": \"C13H25N2\",\n        \"inorganic\": \"PbBr4\",\n        \"iupac\": \"S-\\u03b2-methylphenethylaminium butylaminium lead (II) bromide\",\n        \"last_update\": \"2023-03-21\",\n        \"description\": \"The two cations were mixed in a 1:1 mole ration to make this material.\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"absorption spectrum\",\n        \"primary_unit\": \"a.u\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkyl\\u2013Aryl Cation Mixing in Chiral 2D Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"18114\",\n        \"pages_end\": \"18120\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"butylammonium bromide, S-\\u03b2-methylphenethylamine, hydrobromic acid, PbBr2, \\u03b3-butyrolactone, acetonitrile, ethanol, diethyl ether\",\n        \"synthesis_product\": \"Single crystals of S-\\u03b2-methylphenethylammonium butylammonium lead bromide\",\n        \"synthesis_description\": \"First, S-\\u03b2-methylphenethylamine was mixed with hydrobromic acid (47 wt % in water) with a ratio of 1:1.05 moles. This was done at 0\\u00b0 Celsius for 1 hour, before evaporation of the solvent. The remaining precipitate was dissolved and recrystallized in ethanol, then washed with diethyl ether and vacuum-dried overnight. This resulted in S-MePEABr.\\r\\n\\r\\nNext, S-MePEABr (21.6 mg), butylammonium bromide (15.4 mg), and PbBr2 (36.7 mg) were dissolved in a solvent of \\u03b3-butyrolactone (3 mL) and acetonitrile (9 mL) at a temperature of 80\\u00b0 Celsius. This solution cooled at a rate of 1\\u00b0 / hour down to 10\\u00b0 Celsius. The resulting crystals were clear and plate-like.\",\n        \"experimental_method\": \"UV-vis spectroscopy\",\n        \"experimental_description\": \"Thin films of the material were prepared by spin-casting onto a glass substrate and annealing samples on a hot plate (100\\u00b0 Celsius, 10 mins). A Shimazu UV-2600 was used for measurements.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"https://doi.org/10.1021/jacs.1c06841\",\n        \"dataset_ID\": 2271,\n        \"id\": 523,\n        \"compound_name\": \"S-\\u03b2-methylphenethylammonium butylammonium lead bromide\",\n        \"formula\": \"C13H25N2PbBr4\",\n        \"group\": \"[S-MePEA][C3A]PbBr4\",\n        \"organic\": \"C13H25N2\",\n        \"inorganic\": \"PbBr4\",\n        \"iupac\": \"S-\\u03b2-methylphenethylaminium butylaminium lead (II) bromide\",\n        \"last_update\": \"2023-03-21\",\n        \"description\": \"The two cations were mixed in a 1:1 mole ration to make this material.\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"circular dichroism (CD)\",\n        \"primary_unit\": \"mDegree\",\n        \"secondary_name\": \"wavelength\",\n        \"secondary_unit\": \"nm\",\n        \"visible\": true,\n        \"is_experimental\": true,\n        \"sample_type\": \"film\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"Alkyl\\u2013Aryl Cation Mixing in Chiral 2D Perovskites\",\n        \"journal\": \"Journal of the American Chemical Society\",\n        \"vol\": \"143\",\n        \"pages_start\": \"18114\",\n        \"pages_end\": \"18120\",\n        \"year\": \"2021\",\n        \"synthesis_starting_materials\": \"butylammonium bromide, S-\\u03b2-methylphenethylamine, hydrobromic acid, PbBr2, \\u03b3-butyrolactone, acetonitrile, ethanol, diethyl ether\",\n        \"synthesis_product\": \"Single crystals of S-\\u03b2-methylphenethylammonium butylammonium lead bromide\",\n        \"synthesis_description\": \"First, S-\\u03b2-methylphenethylamine was mixed with hydrobromic acid (47 wt % in water) with a ratio of 1:1.05 moles. This was done at 0\\u00b0 Celsius for 1 hour, before evaporation of the solvent. The remaining precipitate was dissolved and recrystallized in ethanol, then washed with diethyl ether and vacuum-dried overnight. This resulted in S-MePEABr.\\r\\n\\r\\nNext, S-MePEABr (21.6 mg), butylammonium bromide (15.4 mg), and PbBr2 (36.7 mg) were dissolved in a solvent of \\u03b3-butyrolactone (3 mL) and acetonitrile (9 mL) at a temperature of 80\\u00b0 Celsius. This solution cooled at a rate of 1\\u00b0 / hour down to 10\\u00b0 Celsius. The resulting crystals were clear and plate-like.\",\n        \"experimental_method\": \"Circular dichroism spectroscopy\",\n        \"experimental_description\": \"Thin films of the material were prepared by spin-casting onto a glass substrate and annealing samples on a hot plate (100\\u00b0 Celsius, 10 mins). A Chirascan V100 Plus-Spectropolarimeter was used for measurements. The exciton peak was divided by the absorbance to normalize the CD measurement.\",\n        \"physical_property\": \"\",\n        \"unit\": \"\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"-\",\n        \"dataset_ID\": 2272,\n        \"id\": 524,\n        \"compound_name\": \"Bis(2-([2,2'-bithiophen]-5-yl)ethan-1-aminium) methylammonium lead iodide\",\n        \"formula\": \"(C10H12NS2)2CH6NPb2I7\",\n        \"group\": \"2T2MAPb2I7\",\n        \"organic\": \"C10H12NS2, CH6N\",\n        \"inorganic\": \"Pb2I7\",\n        \"iupac\": \"bis(2-([2,2'-bithiophen]-5-yl)ethan-1-aminium) methanaminium lead (II) iodide\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"-\",\n        \"dataset_ID\": 2273,\n        \"id\": 525,\n        \"compound_name\": \"Bis(2-([2,2'-bithiophen]-5-yl)ethan-1-aminium) bis(methylammonium) lead iodide\",\n        \"formula\": \"(C10H12NS2)2(CH6N)2Pb3I10\",\n        \"group\": \"2T2MA2Pb3I10\",\n        \"organic\": \"C10H12NS2, CH6N\",\n        \"inorganic\": \"Pb3I10\",\n        \"iupac\": \"bis(2-([2,2'-bithiophen]-5-yl)ethan-1-aminium) bis(methanaminium) lead (II) iodide\",\n        \"last_update\": \"2023-03-28\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"273.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"-\",\n        \"dataset_ID\": 2274,\n        \"id\": 526,\n        \"compound_name\": \"Bis((2-([2,2':5',2''-terthiophen]-5-yl)ethyl)-l4-azane) lead iodide\",\n        \"formula\": \"(C14H14NS3)2PbI4\",\n        \"group\": \"\",\n        \"organic\": \"C14H14NS3\",\n        \"inorganic\": \"PbI4\",\n        \"iupac\": \"bis((2-([2,2':5',2''-terthiophen]-5-yl)ethyl)-l4-azane) lead (II) iodide\",\n        \"last_update\": \"2023-04-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"-\",\n        \"dataset_ID\": 2275,\n        \"id\": 527,\n        \"compound_name\": \"Bis((2-([2,2':5',2''-terthiophen]-5-yl)ethyl)-l4-azane) methylammonium lead iodide\",\n        \"formula\": \"(C14H14NS3)2CH6NPb2I7\",\n        \"group\": \"\",\n        \"organic\": \"C14H14NS3, CH6N\",\n        \"inorganic\": \"Pb2I7\",\n        \"iupac\": \"bis((2-([2,2':5',2''-terthiophen]-5-yl)ethyl)-l4-azane) methanaminium lead (II) iodide\",\n        \"last_update\": \"2023-04-20\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    },\n    {\n        \"doi_isbn\": \"-\",\n        \"dataset_ID\": 2276,\n        \"id\": 528,\n        \"compound_name\": \"Bis(2-(3''',4'-dimethyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)ethan-1-aminium) methylammonium lead iodide\",\n        \"formula\": \"(C20H20NS4)2CH6NPb2I7\",\n        \"group\": \"\",\n        \"organic\": \"C20H20NS4, CH6N\",\n        \"inorganic\": \"Pb2I7\",\n        \"iupac\": \"bis(2-(3''',4'-dimethyl-[2,2':5',2'':5'',2'''-quaterthiophen]-5-yl)ethan-1-aminium) methanaminium lead (II) iodide\",\n        \"last_update\": \"2023-04-11\",\n        \"description\": \"\",\n        \"message\": \"\",\n        \"dimensionality\": 2,\n        \"n\": \"\",\n        \"derived_to_from\": [],\n        \"tags\": [],\n        \"Related_data_setID\": \"[]\",\n        \"primary_name\": \"atomic structure\",\n        \"primary_unit\": \"\\u00c5\",\n        \"secondary_name\": \"\",\n        \"secondary_unit\": \"\",\n        \"visible\": false,\n        \"is_experimental\": true,\n        \"sample_type\": \"single crystal\",\n        \"representative\": true,\n        \"code\": \"\",\n        \"level_of_theory\": \"\",\n        \"xc_functional\": \"\",\n        \"k_point_grid\": \"\",\n        \"level_of_relativity\": \"\",\n        \"basis_set_definition\": \"\",\n        \"numerical_accuracy\": \"\",\n        \"title\": \"unpublished\",\n        \"journal\": \"-\",\n        \"vol\": \"-\",\n        \"pages_start\": \"-\",\n        \"pages_end\": \"-\",\n        \"year\": \"2023\",\n        \"synthesis_starting_materials\": \"\",\n        \"synthesis_product\": \"\",\n        \"synthesis_description\": \"\",\n        \"experimental_method\": \"\",\n        \"experimental_description\": \"\",\n        \"physical_property\": \"150.0\",\n        \"unit\": \"K\",\n        \"crystal_system\": \"unknown\",\n        \"label\": \"\",\n        \"space_group\": \"\",\n        \"extraction_method\": \"\"\n    }\n]"
  },
  {
    "path": "dataset/ESOL/ESOL.csv",
    "content": "Compound,solubility_log in mol/L (solubility expressed as a logarithm in mol/L),SMILES,SELFIES,InChI\n\"1,1,1,2-Tetrachloroethane\",-2.18,ClCC(Cl)(Cl)Cl,[Cl][C][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C2H2Cl4/c3-1-2(4,5)6/h1H2\"\n\"1,1,1-Trichloroethane\",-2,CC(Cl)(Cl)Cl,[C][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C2H3Cl3/c1-2(3,4)5/h1H3\"\n\"1,1,2,2-Tetrachloroethane\",-1.74,ClC(Cl)C(Cl)Cl,[Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Cl],InChI=1S/C2H2Cl4/c3-1(4)2(5)6/h1-2H\n\"1,1,2-Trichloroethane\",-1.48,ClCC(Cl)Cl,[Cl][C][C][Branch1][C][Cl][Cl],\"InChI=1S/C2H3Cl3/c3-1-2(4)5/h2H,1H2\"\n\"1,1,2-Trichlorotrifluoroethane\",-3.04,FC(F)(Cl)C(F)(Cl)Cl,[F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][Cl][Cl],\"InChI=1S/C2Cl3F3/c3-1(4,6)2(5,7)8\"\n\"1,1-Dichloroethane\",-1.29,CC(Cl)Cl,[C][C][Branch1][C][Cl][Cl],\"InChI=1S/C2H4Cl2/c1-2(3)4/h2H,1H3\"\n\"1,1-Dichloroethylene\",-1.64,ClC(=C)Cl,[Cl][C][=Branch1][C][=C][Cl],InChI=1S/C2H2Cl2/c1-2(3)4/h1H2\n\"1,1-Diethoxyethane \",-0.43,CCOC(C)OCC,[C][C][O][C][Branch1][C][C][O][C][C],\"InChI=1S/C6H14O2/c1-4-7-6(3)8-5-2/h6H,4-5H2,1-3H3\"\n\"1,2,3,4-Tetrachlorobenzene\",-4.57,Clc1ccc(Cl)c(Cl)c1Cl,[Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl],InChI=1S/C6H2Cl4/c7-3-1-2-4(8)6(10)5(3)9/h1-2H\n\"1,2,3,4-Tetrahydronapthalene\",-4.37,C1CCc2ccccc2C1,[C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2],\"InChI=1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2\"\n\"1,2,3,5-Tetrachlorobenzene\",-4.63,Clc1cc(Cl)c(Cl)c(Cl)c1,[Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2],InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)5(9)2-3/h1-2H\n\"1,2,3-Trichlorobenzene\",-4,Clc1cccc(Cl)c1Cl,[Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl],InChI=1S/C6H3Cl3/c7-4-2-1-3-5(8)6(4)9/h1-3H\n\"1,2,3-Trimethylbenzene \",-3.2,Cc1cccc(C)c1C,[C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C],\"InChI=1S/C9H12/c1-7-5-4-6-8(2)9(7)3/h4-6H,1-3H3\"\n\"1,2,4,5-Tetrabromobenzene\",-6.98,Brc1cc(Br)c(Br)cc1Br,[Br][C][=C][C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Br],InChI=1S/C6H2Br4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\n\"1,2,4,5-Tetrachlorobenzene\",-5.56,Clc1cc(Cl)c(Cl)cc1Cl,[Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl],InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\n\"1,2,4,5-Tetramethylbenzene\",-4.59,Cc1cc(C)c(C)cc1C,[C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][=C][Ring1][Branch2][C],\"InChI=1S/C10H14/c1-7-5-9(3)10(4)6-8(7)2/h5-6H,1-4H3\"\n\"1,2,4-tribromobenzene\",-4.5,c1(Br)c(Br)cc(Br)cc1,[C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Branch1][C][Br][C][=C][Ring1][=Branch2],InChI=1S/C6H3Br3/c7-4-1-2-5(8)6(9)3-4/h1-3H\n\"1,2,4-Trichlorobenzene\",-3.59,Clc1ccc(Cl)c(Cl)c1,[Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],InChI=1S/C6H3Cl3/c7-4-1-2-5(8)6(9)3-4/h1-3H\n\"1,2,4-Trimethylbenzene\",-3.31,Cc1ccc(C)c(C)c1,[C][C][=C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][Branch2],\"InChI=1S/C9H12/c1-7-4-5-8(2)9(3)6-7/h4-6H,1-3H3\"\n\"1,2-Benzenediol\",0.62,Oc1ccccc1O,[O][C][=C][C][=C][C][=C][Ring1][=Branch1][O],\"InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H\"\n\"1,2-Dibromobenzene\",-3.5,Brc1ccccc1Br,[Br][C][=C][C][=C][C][=C][Ring1][=Branch1][Br],InChI=1S/C6H4Br2/c7-5-3-1-2-4-6(5)8/h1-4H\n\"1,2-Dibromoethane\",-1.68,BrCCBr,[Br][C][C][Br],InChI=1S/C2H4Br2/c3-1-2-4/h1-2H2\n\"1,2-Dichlorobenzene\",-3.05,Clc1ccccc1Cl,[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],InChI=1S/C6H4Cl2/c7-5-3-1-2-4-6(5)8/h1-4H\n\"1,2-Dichloroethane\",-1.06,ClCCCl,[Cl][C][C][Cl],InChI=1S/C2H4Cl2/c3-1-2-4/h1-2H2\n\"1,2-Dichloropropane\",-1.6,CC(Cl)CCl,[C][C][Branch1][C][Cl][C][Cl],\"InChI=1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3\"\n\"1,2-Dichlorotetrafluoroethane\",-2.74,FC(F)(Cl)C(F)(F)Cl,[F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][Cl],\"InChI=1S/C2Cl2F4/c3-1(5,6)2(4,7)8\"\n\"1,2-Diethoxyethane \",-0.77,CCOCCOCC,[C][C][O][C][C][O][C][C],\"InChI=1S/C6H14O2/c1-3-7-5-6-8-4-2/h3-6H2,1-2H3\"\n\"1,2-Diethylbenzene\",-3.28,CCc1ccccc1CC,[C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C],\"InChI=1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3\"\n\"1,2-Dinitrobenzene\",-3.1,O=N(=O)c1ccccc1N(=O)=O,[O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],InChI=1S/C6H4N2O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H\n\"1,2-Propylene oxide\",-0.59,CC1CO1,[C][C][C][O][Ring1][Ring1],\"InChI=1S/C3H6O/c1-3-2-4-3/h3H,2H2,1H3\"\n\"1,3,5-Tribromobenzene\",-5.6,Brc1cc(Br)cc(Br)c1,[Br][C][=C][C][Branch1][C][Br][=C][C][Branch1][C][Br][=C][Ring1][Branch2],InChI=1S/C6H3Br3/c7-4-1-5(8)3-6(9)2-4/h1-3H\n\"1,3,5-Trichlorobenzene\",-4.48,Clc1cc(Cl)cc(Cl)c1,[Cl][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2],InChI=1S/C6H3Cl3/c7-4-1-5(8)3-6(9)2-4/h1-3H\n\"1,3,5-Trimethylbenzene \",-3.4,Cc1cc(C)cc(C)c1,[C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2],\"InChI=1S/C9H12/c1-7-4-8(2)6-9(3)5-7/h4-6H,1-3H3\"\n\"1,3,5-Trinitrobenzene\",-2.89,O=N(=O)c1cc(cc(c1)N(=O)=O)N(=O)=O,[O][=N][=Branch1][C][=O][C][=C][C][=Branch1][=N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O],InChI=1S/C6H3N3O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H\n\"1,3-Benzenediol\",0.81,Oc1cccc(O)c1,[O][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1],\"InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H\"\n\"1,3-Butadiene\",-1.87,C=CC=C,[C][=C][C][=C],\"InChI=1S/C4H6/c1-3-4-2/h3-4H,1-2H2\"\n\"1,3-Dibromobenzene\",-3.54,Brc1cccc(Br)c1,[Br][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1],InChI=1S/C6H4Br2/c7-5-2-1-3-6(8)4-5/h1-4H\n\"1,3-Dichlorobenzene\",-3.04,Clc1cccc(Cl)c1,[Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],InChI=1S/C6H4Cl2/c7-5-2-1-3-6(8)4-5/h1-4H\n\"1,3-Dichloropropane\",-1.62,ClCCCCl,[Cl][C][C][C][Cl],InChI=1S/C3H6Cl2/c4-2-1-3-5/h1-3H2\n\"1,3-diethylthiourea\",-1.46,CCNC(=S)NCC,[C][C][N][C][=Branch1][C][=S][N][C][C],\"InChI=1S/C5H12N2S/c1-3-6-5(8)7-4-2/h3-4H2,1-2H3,(H2,6,7,8)\"\n\"1,3-Difluorobenzene\",-2,Fc1cccc(F)c1,[F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1],InChI=1S/C6H4F2/c7-5-2-1-3-6(8)4-5/h1-4H\n\"1,3-Dimethylnaphthalene\",-4.29,Cc1cc(C)c2ccccc2c1,[C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O],\"InChI=1S/C12H12/c1-9-7-10(2)12-6-4-3-5-11(12)8-9/h3-8H,1-2H3\"\n\"1,3-Dinitrobenzene\",-2.29,O=N(=O)c1cccc(c1)N(=O)=O,[O][=N][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],InChI=1S/C6H4N2O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H\n\"1,4-Benzenediol\",-0.17,Oc1ccc(O)cc1,[O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H\"\n\"1,4-Cyclohexadiene\",-2.06,C1C=CCC=C1,[C][C][=C][C][C][=C][Ring1][=Branch1],\"InChI=1S/C6H8/c1-2-4-6-5-3-1/h1-2,5-6H,3-4H2\"\n\"1,4-Dibromobenzene\",-4.07,Brc1ccc(Br)cc1,[Br][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],InChI=1S/C6H4Br2/c7-5-1-2-6(8)4-3-5/h1-4H\n\"1,4-Dichlorobenzene\",-3.27,Clc1ccc(Cl)cc1,[Cl][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],InChI=1S/C6H4Cl2/c7-5-1-2-6(8)4-3-5/h1-4H\n\"1,4-Diethylbenzene \",-3.75,CCc1ccc(CC)cc1,[C][C][C][=C][C][=C][Branch1][Ring1][C][C][C][=C][Ring1][Branch2],\"InChI=1S/C10H14/c1-3-9-5-7-10(4-2)8-6-9/h5-8H,3-4H2,1-2H3\"\n\"1,4-Difluorobenzene\",-1.97,Fc1ccc(F)cc1,[F][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],InChI=1S/C6H4F2/c7-5-1-2-6(8)4-3-5/h1-4H\n\"1,4-Dimethylnaphthalene \",-4.14,Cc1ccc(C)c2ccccc12,[C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1],\"InChI=1S/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3\"\n\"1,4-Dinitrobenzene\",-3.39,O=N(=O)c1ccc(cc1)N(=O)=O,[O][=N][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],InChI=1S/C6H4N2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H\n\"1,4-Pentadiene \",-2.09,C=CCC=C,[C][=C][C][C][=C],\"InChI=1S/C5H8/c1-3-5-4-2/h3-4H,1-2,5H2\"\n\"1,5-Dimethlnapthalene\",-4.679,Cc1cccc2c(C)cccc12,[C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][O][Ring1][#Branch1],\"InChI=1S/C12H12/c1-9-5-3-8-12-10(2)6-4-7-11(9)12/h3-8H,1-2H3\"\n\"1,5-Hexadiene \",-2.68,C=CCCC=C,[C][=C][C][C][C][=C],\"InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2\"\n\"1,7-phenantroline\",-2.68,c1cnc2c(c1)ccc3ncccc23,[C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][C][=C][Ring1][O][Ring1][=Branch1],InChI=1S/C12H8N2/c1-3-9-5-6-11-10(4-2-7-13-11)12(9)14-8-1/h1-8H\n\"1,8-Cineole\",-1.74,CC12CCC(CC1)C(C)(C)O2,[C][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][O][Ring1][#Branch2],\"InChI=1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3\"\n17a-Methyltestosterone,-3.999,CC1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C,[C][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C],\"InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3\"\n1-Bromo-2-methylpropane,-2.43,CC(C)CBr,[C][C][Branch1][C][C][C][Br],\"InChI=1S/C4H9Br/c1-4(2)3-5/h4H,3H2,1-2H3\"\n1-Bromobutane,-2.37,CCCCBr,[C][C][C][C][Br],\"InChI=1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3\"\n1-Bromoheptane,-4.43,CCCCCCCBr,[C][C][C][C][C][C][C][Br],\"InChI=1S/C7H15Br/c1-2-3-4-5-6-7-8/h2-7H2,1H3\"\n1-Bromohexane,-3.81,CCCCCCBr,[C][C][C][C][C][C][Br],\"InChI=1S/C6H13Br/c1-2-3-4-5-6-7/h2-6H2,1H3\"\n1-Bromonapthalene,-4.35,Brc1cccc2ccccc12,[Br][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\n1-Bromooctane,-5.06,CCCCCCCCBr,[C][C][C][C][C][C][C][C][Br],\"InChI=1S/C8H17Br/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3\"\n1-Bromopentane,-3.08,CCCCCBr,[C][C][C][C][C][Br],\"InChI=1S/C5H11Br/c1-2-3-4-5-6/h2-5H2,1H3\"\n1-Bromopropane,-1.73,CCCBr,[C][C][C][Br],\"InChI=1S/C3H7Br/c1-2-3-4/h2-3H2,1H3\"\n1-Butanol,0,CCCCO,[C][C][C][C][O],\"InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3\"\n1-Butene,-1.94,CCC=C,[C][C][C][=C],\"InChI=1S/C4H8/c1-3-4-2/h3H,1,4H2,2H3\"\n1-Butyne,-1.24,CCC#C,[C][C][C][#C],\"InChI=1S/C4H6/c1-3-4-2/h1H,4H2,2H3\"\n1-Chloro-2-bromoethane,-1.32,ClCCBr,[Cl][C][C][Br],InChI=1S/C2H4BrCl/c3-1-2-4/h1-2H2\n1-Chloro-2-methylpropane,-2,ClCC(C)C,[Cl][C][C][Branch1][C][C][C],\"InChI=1S/C4H9Cl/c1-4(2)3-5/h4H,3H2,1-2H3\"\n1-Chlorobutane,-2.03,CCCCCl,[C][C][C][C][Cl],\"InChI=1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3\"\n1-Chloroheptane,-4,CCCCCCCCl,[C][C][C][C][C][C][C][Cl],\"InChI=1S/C7H15Cl/c1-2-3-4-5-6-7-8/h2-7H2,1H3\"\n1-Chlorohexane,-3.12,CCCCCCCl,[C][C][C][C][C][C][Cl],\"InChI=1S/C6H13Cl/c1-2-3-4-5-6-7/h2-6H2,1H3\"\n1-Chloronapthalene,-3.93,Clc1cccc2ccccc12,[Cl][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C10H7Cl/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\n1-Chloropentane,-2.73,CCCCCCl,[C][C][C][C][C][Cl],\"InChI=1S/C5H11Cl/c1-2-3-4-5-6/h2-5H2,1H3\"\n1-Chloropropane,-1.47,CCCCl,[C][C][C][Cl],\"InChI=1S/C3H7Cl/c1-2-3-4/h2-3H2,1H3\"\n1-Decanol,-3.63,CCCCCCCCCCO,[C][C][C][C][C][C][C][C][C][C][O],\"InChI=1S/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3\"\n1-Decene,-5.51,CCCCCCCCC=C,[C][C][C][C][C][C][C][C][C][=C],\"InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3\"\n1-Dodecanol,-4.8,CCCCCCCCCCCCO,[C][C][C][C][C][C][C][C][C][C][C][C][O],\"InChI=1S/C12H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-12H2,1H3\"\n1-Ethylnaphthalene ,-4.17,CCc1cccc2ccccc12,[C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"InChI=1S/C12H12/c1-2-10-7-5-8-11-6-3-4-9-12(10)11/h3-9H,2H2,1H3\"\n1-Heptanol,-1.81,CCCCCCCO,[C][C][C][C][C][C][C][O],\"InChI=1S/C7H16O/c1-2-3-4-5-6-7-8/h8H,2-7H2,1H3\"\n1-Heptene,-3.73,CCCCCC=C,[C][C][C][C][C][C][=C],\"InChI=1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3\"\n1-Heptyne,-3.01,CCCCCC#C,[C][C][C][C][C][C][#C],\"InChI=1S/C7H12/c1-3-5-7-6-4-2/h1H,4-7H2,2H3\"\n1-Hexadecanol,-7,CCCCCCCCCCCCCCCCO,[C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O],\"InChI=1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3\"\n1-Hexanol,-1.24,CCCCCCO,[C][C][C][C][C][C][O],\"InChI=1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3\"\n1-Hexene,-3.23,CCCCC=C,[C][C][C][C][C][=C],\"InChI=1S/C6H12/c1-3-5-6-4-2/h3H,1,4-6H2,2H3\"\n1-Hexene-3-ol,-0.59,CCCC(O)C=C,[C][C][C][C][Branch1][C][O][C][=C],\"InChI=1S/C6H12O/c1-3-5-6(7)4-2/h4,6-7H,2-3,5H2,1H3\"\n1-Hexyne ,-2.36,CCCCC#C,[C][C][C][C][C][#C],\"InChI=1S/C6H10/c1-3-5-6-4-2/h1H,4-6H2,2H3\"\n1-Iodobutane,-2.96,CCCCI,[C][C][C][C][I],\"InChI=1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3\"\n1-Iodoheptane,-4.81,CCCCCCCI,[C][C][C][C][C][C][C][I],\"InChI=1S/C7H15I/c1-2-3-4-5-6-7-8/h2-7H2,1H3\"\n1-Iodonapthalene,-4.55,Ic1cccc2ccccc12,[I][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C10H7I/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\n1-Iodopropane,-2.29,CCCI,[C][C][C][I],\"InChI=1S/C3H7I/c1-2-3-4/h2-3H2,1H3\"\n1-Methylcyclohexene ,-3.27,CC1=CCCCC1,[C][C][=C][C][C][C][C][Ring1][=Branch1],\"InChI=1S/C7H12/c1-7-5-3-2-4-6-7/h5H,2-4,6H2,1H3\"\n1-Methylfluorene,-5.22,Cc1cccc2c1Cc3ccccc32,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][=Branch2],\"InChI=1S/C14H12/c1-10-5-4-8-13-12-7-3-2-6-11(12)9-14(10)13/h2-8H,9H2,1H3\"\n1-Methylnaphthalene,-3.7,Cc1cccc2ccccc12,[C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"InChI=1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3\"\n1-Methylphenanthrene,-5.85,Cc1cccc2c1ccc3ccccc32,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2],\"InChI=1S/C15H12/c1-11-5-4-8-15-13(11)10-9-12-6-2-3-7-14(12)15/h2-10H,1H3\"\n1-methyluracil,-0.807,Cn1ccc(=O)[nH]c1=O,[C][N][C][=C][C][=Branch1][C][=O][NH1][C][Ring1][#Branch1][=O],\"InChI=1S/C5H6N2O2/c1-7-3-2-4(8)6-5(7)9/h2-3H,1H3,(H,6,8,9)\"\n1-Napthol,-2.22,Oc1cccc2ccccc12,[O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H\"\n1-Napthylamine,-1.92,Nc1cccc2ccccc12,[N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2\"\n1-Nitronapthalene,-3.54,O=N(=O)c1cccc2ccccc12,[O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C10H7NO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\n1-Nitropropane,-0.8,CCCN(=O)=O,[C][C][C][N][=Branch1][C][=O][=O],\"InChI=1S/C3H7NO2/c1-2-3-4(5)6/h2-3H2,1H3\"\n1-Nonanol,-3.01,CCCCCCCCCO,[C][C][C][C][C][C][C][C][C][O],\"InChI=1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3\"\n1-Nonene ,-5.05,CCCCCCCC=C,[C][C][C][C][C][C][C][C][=C],\"InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3\"\n1-Nonyne ,-4.24,CCCCCCCC#C,[C][C][C][C][C][C][C][C][#C],\"InChI=1S/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H3\"\n1-Octadecanol,-8.4,CCCCCCCCCCCCCCCCCCO,[C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O],\"InChI=1S/C18H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h19H,2-18H2,1H3\"\n1-Octanol,-2.39,CCCCCCCCO,[C][C][C][C][C][C][C][C][O],\"InChI=1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3\"\n1-Octene ,-4.44,CCCCCCC=C,[C][C][C][C][C][C][C][=C],\"InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3\"\n1-Octyne ,-3.66,CCCCCCC#C,[C][C][C][C][C][C][C][#C],\"InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h1H,4-8H2,2H3\"\n1-Pentadecanol,-6.35,CCCCCCCCCCCCCCCO,[C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O],\"InChI=1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3\"\n1-Pentanol,-0.6,CCCCCO,[C][C][C][C][C][O],\"InChI=1S/C5H12O/c1-2-3-4-5-6/h6H,2-5H2,1H3\"\n1-Pentene ,-2.68,CCCC=C,[C][C][C][C][=C],\"InChI=1S/C5H10/c1-3-5-4-2/h3H,1,4-5H2,2H3\"\n1-Pentyne,-1.64,CCCC#C,[C][C][C][C][#C],\"InChI=1S/C5H8/c1-3-5-4-2/h1H,4-5H2,2H3\"\n1-Phenylethanol,-0.92,CC(O)c1ccccc1,[C][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3\"\n1-Propanol,0.62,CCCO,[C][C][C][O],\"InChI=1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3\"\n1-Tetradecanol,-5.84,CCCCCCCCCCCCCCO,[C][C][C][C][C][C][C][C][C][C][C][C][C][C][O],\"InChI=1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3\"\n\"2,2',3,3',4,4',5,5'-PCB\",-9.16,Clc1cc(c(Cl)c(Cl)c1Cl)c2cc(Cl)c(Cl)c(Cl)c2Cl,[Cl][C][=C][C][=Branch1][=N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl],InChI=1S/C12H2Cl8/c13-5-1-3(7(15)11(19)9(5)17)4-2-6(14)10(18)12(20)8(4)16/h1-2H\n\"2,2',3,3'-PCB\",-7.28,Clc1cccc(c1Cl)c2cccc(Cl)c2Cl,[Cl][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring1][=Branch1][Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl],InChI=1S/C12H6Cl4/c13-9-5-1-3-7(11(9)15)8-4-2-6-10(14)12(8)16/h1-6H\n\"2,2',3,4,4',5',6-PCB\",-7.92,Clc1ccc(c(Cl)c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl,[Cl][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl],InChI=1S/C12H3Cl7/c13-4-1-2-5(6(14)3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\n\"2,2',3,4,5,5',6-PCB\",-8.94,Clc1ccc(Cl)c(c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl,[Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl],InChI=1S/C12H3Cl7/c13-4-1-2-6(14)5(3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\n\"2,2',3,4,5,5'-PCB\",-7.68,Clc1ccc(Cl)c(c1)c2cc(Cl)c(Cl)c(Cl)c2Cl,[Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl],InChI=1S/C12H4Cl6/c13-5-1-2-8(14)6(3-5)7-4-9(15)11(17)12(18)10(7)16/h1-4H\n\"2,2,3-Trimethylbutane\",-4.36,CC(C)C(C)(C)C,[C][C][Branch1][C][C][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C7H16/c1-6(2)7(3,4)5/h6H,1-5H3\"\n\"2,2,4,6,6'-PCB\",-7.32,Clc1cc(Cl)c(c(Cl)c1)c2c(Cl)cccc2Cl,[Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl],InChI=1S/C12H5Cl5/c13-6-4-9(16)12(10(17)5-6)11-7(14)2-1-3-8(11)15/h1-5H\n\"2,2,4-Trimethylpentane\",-4.74,CC(C)CC(C)(C)C,[C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C8H18/c1-7(2)6-8(3,4)5/h7H,6H2,1-5H3\"\n\"2,2,5-Trimethylhexane\",-5.05,CC(C)CCC(C)(C)C,[C][C][Branch1][C][C][C][C][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C9H20/c1-8(2)6-7-9(3,4)5/h8H,6-7H2,1-5H3\"\n\"2,2-Dimethyl-1-butanol\",-1.04,CCC(C)(C)CO,[C][C][C][Branch1][C][C][Branch1][C][C][C][O],\"InChI=1S/C6H14O/c1-4-6(2,3)5-7/h7H,4-5H2,1-3H3\"\n\"2,2-Dimethylbutane\",-3.55,CCC(C)(C)C,[C][C][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C6H14/c1-5-6(2,3)4/h5H2,1-4H3\"\n\"2,2-Dimethylpentane\",-4.36,CCCC(C)(C)C,[C][C][C][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C7H16/c1-5-6-7(2,3)4/h5-6H2,1-4H3\"\n\"2,2-Dimethylpentanol\",-1.52,CCCC(C)(C)CO,[C][C][C][C][Branch1][C][C][Branch1][C][C][C][O],\"InChI=1S/C7H16O/c1-4-5-7(2,3)6-8/h8H,4-6H2,1-3H3\"\n\"2,2-Dimethylpropanol\",-0.4,CC(C)(C)CO,[C][C][Branch1][C][C][Branch1][C][C][C][O],\"InChI=1S/C5H12O/c1-5(2,3)4-6/h6H,4H2,1-3H3\"\n\"2,3',4',5-PCB\",-7.25,Clc1ccc(Cl)c(c1)c2ccc(Cl)c(Cl)c2,[Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],InChI=1S/C12H6Cl4/c13-8-2-4-10(14)9(6-8)7-1-3-11(15)12(16)5-7/h1-6H\n\"2,3,4,5-Tetrachlorophenol\",-3.15,Oc1cc(Cl)c(Cl)c(Cl)c1Cl,[O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl],\"InChI=1S/C6H2Cl4O/c7-2-1-3(11)5(9)6(10)4(2)8/h1,11H\"\n\"2,3,4,6-Tetrachlorophenol\",-3.1,Oc1c(Cl)cc(Cl)c(Cl)c1Cl,[O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl],\"InChI=1S/C6H2Cl4O/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H\"\n\"2,3,4-Trichlorophenol\",-2.67,Oc1ccc(Cl)c(Cl)c1Cl,[O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl],\"InChI=1S/C6H3Cl3O/c7-3-1-2-4(10)6(9)5(3)8/h1-2,10H\"\n\"2,3,4-Trimethylpentane\",-4.8,CC(C)C(C)C(C)C,[C][C][Branch1][C][C][C][Branch1][C][C][C][Branch1][C][C][C],\"InChI=1S/C8H18/c1-6(2)8(5)7(3)4/h6-8H,1-5H3\"\n\"2,3,5,6-Tetrachlorophenol\",-3.37,Oc1c(Cl)c(Cl)cc(Cl)c1Cl,[O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl],\"InChI=1S/C6H2Cl4O/c7-2-1-3(8)5(10)6(11)4(2)9/h1,11H\"\n\"2,3,5-Trichlorophenol\",-2.67,Oc1cc(Cl)cc(Cl)c1Cl,[O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl],\"InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(9)5(10)2-3/h1-2,10H\"\n\"2,3,6-Trichlorophenol\",-2.64,Oc1c(Cl)ccc(Cl)c1Cl,[O][C][=C][Branch1][C][Cl][C][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl],\"InChI=1S/C6H3Cl3O/c7-3-1-2-4(8)6(10)5(3)9/h1-2,10H\"\n\"2,3-Dichloronitrobenzene\",-3.48,O=N(=O)c1c(Cl)c(Cl)ccc1,[O][=N][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][=C][Ring1][Branch2],InChI=1S/C6H3Cl2NO2/c7-4-2-1-3-5(6(4)8)9(10)11/h1-3H\n\"2,3-Dichlorophenol\",-1.3,Oc1cccc(Cl)c1Cl,[O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl],\"InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H\"\n\"2,3-Dimethyl-1,3-Butadiene\",-2.4,CC(=C)C(=C)C,[C][C][=Branch1][C][=C][C][=Branch1][C][=C][C],\"InChI=1S/C6H10/c1-5(2)6(3)4/h1,3H2,2,4H3\"\n\"2,3-Dimethylbutane\",-3.65,CC(C)C(C)C,[C][C][Branch1][C][C][C][Branch1][C][C][C],\"InChI=1S/C6H14/c1-5(2)6(3)4/h5-6H,1-4H3\"\n\"2,3-Dimethylnaphthalene\",-4.72,Cc1cc2ccccc2cc1C,[C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][C],\"InChI=1S/C12H12/c1-9-7-11-5-3-4-6-12(11)8-10(9)2/h3-8H,1-2H3\"\n\"2,3-Dimethylpentane\",-4.28,CCC(C)C(C)C,[C][C][C][Branch1][C][C][C][Branch1][C][C][C],\"InChI=1S/C7H16/c1-5-7(4)6(2)3/h6-7H,5H2,1-4H3\"\n\"2,3-Dimethylpyridine\",0.38,Cc1cccnc1C,[C][C][=C][C][=C][N][=C][Ring1][=Branch1][C],\"InChI=1S/C7H9N/c1-6-4-3-5-8-7(6)2/h3-5H,1-2H3\"\n\"2,4,5-Trichlorophenol \",-2.21,Oc1cc(Cl)c(Cl)cc1Cl,[O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl],\"InChI=1S/C6H3Cl3O/c7-3-1-5(9)6(10)2-4(3)8/h1-2,10H\"\n\"2,4,6-Trichlorophenol\",-2.34,Oc1c(Cl)cc(Cl)cc1Cl,[O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl],\"InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H\"\n\"2,4,6-Trimethylphenol\",-2.05,Cc1cc(C)c(O)c(C)c1,[C][C][=C][C][Branch1][C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][=Branch2],\"InChI=1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3\"\n\"2,4,6-Trinitrotoluene\",-3.22,Cc1c(cc(cc1N(=O)=O)N(=O)=O)N(=O)=O,[C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O],\"InChI=1S/C7H5N3O6/c1-4-6(9(13)14)2-5(8(11)12)3-7(4)10(15)16/h2-3H,1H3\"\n\"2,4-Dichlorophenol \",-1.55,Oc1ccc(Cl)cc1Cl,[O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl],\"InChI=1S/C6H4Cl2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H\"\n\"2,4-Dimethyl-2-pentanol \",-0.92,CC(C)CC(C)(C)O,[C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][O],\"InChI=1S/C7H16O/c1-6(2)5-7(3,4)8/h6,8H,5H2,1-4H3\"\n\"2,4-Dimethyl-3-pentanol\",-1.22,CC(C)C(O)C(C)C,[C][C][Branch1][C][C][C][Branch1][C][O][C][Branch1][C][C][C],\"InChI=1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3\"\n\"2,4-Dimethyl-3-pentanone\",-1.3,CC(C)C(=O)C(C)C,[C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][C][C][C],\"InChI=1S/C7H14O/c1-5(2)7(8)6(3)4/h5-6H,1-4H3\"\n\"2,4-Dimethylpentane\",-4.26,CC(C)CC(C)C,[C][C][Branch1][C][C][C][C][Branch1][C][C][C],\"InChI=1S/C7H16/c1-6(2)5-7(3)4/h6-7H,5H2,1-4H3\"\n\"2,4-Dimethylphenol\",-1.19,Cc1ccc(O)c(C)c1,[C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][Branch2],\"InChI=1S/C8H10O/c1-6-3-4-8(9)7(2)5-6/h3-5,9H,1-2H3\"\n\"2,4-Dimethylpyridine\",0.38,Cc1ccnc(C)c1,[C][C][=C][C][=N][C][Branch1][C][C][=C][Ring1][#Branch1],\"InChI=1S/C7H9N/c1-6-3-4-8-7(2)5-6/h3-5H,1-2H3\"\n\"2,4-Dinitrotoluene\",-2.82,Cc1ccc(cc1N(=O)=O)N(=O)=O,[C][C][=C][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O],\"InChI=1S/C7H6N2O4/c1-5-2-3-6(8(10)11)4-7(5)9(12)13/h2-4H,1H3\"\n\"2,6-Dichlorophenol\",-1.79,Oc1c(Cl)cccc1Cl,[O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl],\"InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H\"\n\"2,6-Dimethylnaphthalene \",-4.89,Cc1ccc2cc(C)ccc2c1,[C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][Ring1][#Branch1][=C][Ring1][O],\"InChI=1S/C12H12/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h3-8H,1-2H3\"\n\"2,6-Dimethylphenol\",-1.29,Cc1cccc(C)c1O,[C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O],\"InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3\"\n\"2,6-Dimethylpyridine\",0.45,Cc1cccc(C)n1,[C][C][=C][C][=C][C][Branch1][C][C][=N][Ring1][#Branch1],\"InChI=1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3\"\n\"2,6-Dinitrotoluene\",-3,Cc1c(cccc1N(=O)=O)N(=O)=O,[C][C][=C][Branch1][N][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O],\"InChI=1S/C7H6N2O4/c1-5-6(8(10)11)3-2-4-7(5)9(12)13/h2-4H,1H3\"\n2-Bromonapthalene,-4.4,Brc1ccc2ccccc2c1,[Br][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],InChI=1S/C10H7Br/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\n2-Bromopropane,-1.59,CC(C)Br,[C][C][Branch1][C][C][Br],\"InChI=1S/C3H7Br/c1-3(2)4/h3H,1-2H3\"\n2-Bromotoluene,-2.23,Cc1ccccc1Br,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][Br],\"InChI=1S/C7H7Br/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\"\n2-Butanone,0.52,CCC(=O)C,[C][C][C][=Branch1][C][=O][C],\"InChI=1S/C4H8O/c1-3-4(2)5/h3H2,1-2H3\"\n2-butenal,0.32,CC=CC=O,[C][C][=C][C][=O],\"InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3\"\n2-Butoxyethanol,-0.42,CCCCOCCO,[C][C][C][C][O][C][C][O],\"InChI=1S/C6H14O2/c1-2-3-5-8-6-4-7/h7H,2-6H2,1H3\"\n2-Chloro-2-methylbutane,-2.51,CCC(C)(C)Cl,[C][C][C][Branch1][C][C][Branch1][C][C][Cl],\"InChI=1S/C5H11Cl/c1-4-5(2,3)6/h4H2,1-3H3\"\n2-Chloroanisole,-2.46,COc1ccccc1Cl,[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],\"InChI=1S/C7H7ClO/c1-9-7-5-3-2-4-6(7)8/h2-5H,1H3\"\n2-Chlorobiphenyl,-4.54,Clc1ccccc1c2ccccc2,[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C12H9Cl/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H\n2-Chlorobutane,-1.96,CCC(C)Cl,[C][C][C][Branch1][C][C][Cl],\"InChI=1S/C4H9Cl/c1-3-4(2)5/h4H,3H2,1-2H3\"\n2-Chloronapthalene,-4.14,Clc1ccc2ccccc2c1,[Cl][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],InChI=1S/C10H7Cl/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\n2-Chlorophenol,-1.06,Oc1ccccc1Cl,[O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],\"InChI=1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H\"\n2-Chloropropane,-1.41,CC(C)Cl,[C][C][Branch1][C][C][Cl],\"InChI=1S/C3H7Cl/c1-3(2)4/h3H,1-2H3\"\n2-Chlorotoluene,-3.52,Cc1ccccc1Cl,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],\"InChI=1S/C7H7Cl/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\"\n2-Decanone,-3.3,CCCCCCCCC(=O)C,[C][C][C][C][C][C][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C10H20O/c1-3-4-5-6-7-8-9-10(2)11/h3-9H2,1-2H3\"\n2-Ethyl pyridine,0.51,CCc1ccccn1,[C][C][C][=C][C][=C][C][=N][Ring1][=Branch1],\"InChI=1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3\"\n2-Ethyl-1-butanol,-1.17,CCC(CC)CO,[C][C][C][Branch1][Ring1][C][C][C][O],\"InChI=1S/C6H14O/c1-3-6(4-2)5-7/h6-7H,3-5H2,1-2H3\"\n2-Ethyl-1-hexanol,-2.11,CCCCC(CC)CO,[C][C][C][C][C][Branch1][Ring1][C][C][C][O],\"InChI=1S/C8H18O/c1-3-5-6-8(4-2)7-9/h8-9H,3-7H2,1-2H3\"\n2-Ethyl-2-hexanal,-2.46,CCCC=C(CC)C=O,[C][C][C][C][=C][Branch1][Ring1][C][C][C][=O],\"InChI=1S/C8H14O/c1-3-5-6-8(4-2)7-9/h6-7H,3-5H2,1-2H3\"\n2-Ethylbutanal,-1.52,CCC(CC)C=O,[C][C][C][Branch1][Ring1][C][C][C][=O],\"InChI=1S/C6H12O/c1-3-6(4-2)5-7/h5-6H,3-4H2,1-2H3\"\n2-Ethylhexanal,-2.13,CCCCC(CC)C=O,[C][C][C][C][C][Branch1][Ring1][C][C][C][=O],\"InChI=1S/C8H16O/c1-3-5-6-8(4-2)7-9/h7-8H,3-6H2,1-2H3\"\n2-Ethylnaphthalene,-4.29,CCc1ccc2ccccc2c1,[C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"InChI=1S/C12H12/c1-2-10-7-8-11-5-3-4-6-12(11)9-10/h3-9H,2H2,1H3\"\n2-Ethyltoluene,-3.21,CCc1ccccc1C,[C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C],\"InChI=1S/C9H12/c1-3-9-7-5-4-6-8(9)2/h4-7H,3H2,1-2H3\"\n2-Heptanol ,-1.55,CCCCCC(C)O,[C][C][C][C][C][C][Branch1][C][C][O],\"InChI=1S/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3\"\n2-Heptanone,-1.45,CCCCCC(=O)C,[C][C][C][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H3\"\n2-Hexanol,-0.89,CCCCC(C)O,[C][C][C][C][C][Branch1][C][C][O],\"InChI=1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3\"\n2-Hexanone,-0.8,CCCCC(=O)C,[C][C][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C6H12O/c1-3-4-5-6(2)7/h3-5H2,1-2H3\"\n2-hydroxypteridine,-1.947,Oc2ncc1nccnc1n2,[O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"InChI=1S/C6H4N4O/c11-6-9-3-4-5(10-6)8-2-1-7-4/h1-3H,(H,8,9,10,11)\"\n2-Hydroxypyridine,1.02,Oc1ccccn1,[O][C][=C][C][=C][C][=N][Ring1][=Branch1],\"InChI=1S/C5H5NO/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)\"\n2-Iodopropane,-2.09,CC(C)I,[C][C][Branch1][C][C][I],\"InChI=1S/C3H7I/c1-3(2)4/h3H,1-2H3\"\n2-Isopropyltoluene,-3.76,CC(C)c1ccccc1C,[C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C],\"InChI=1S/C10H14/c1-8(2)10-7-5-4-6-9(10)3/h4-8H,1-3H3\"\n2-methoxypteridine,-1.11,COc2ncc1nccnc1n2,[C][O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"InChI=1S/C7H6N4O/c1-12-7-10-4-5-6(11-7)9-3-2-8-5/h2-4H,1H3\"\n2-Methy-2-Butene,-2.56,CC=C(C)C,[C][C][=C][Branch1][C][C][C],\"InChI=1S/C5H10/c1-4-5(2)3/h4H,1-3H3\"\n\"2-Methyl-1,3-Butadiene \",-2.03,CC(=C)C=C,[C][C][=Branch1][C][=C][C][=C],\"InChI=1S/C5H8/c1-4-5(2)3/h4H,1-2H2,3H3\"\n2-Methyl-1-Butene,-2.73,CCC(=C)C,[C][C][C][=Branch1][C][=C][C],\"InChI=1S/C5H10/c1-4-5(2)3/h2,4H2,1,3H3\"\n2-Methyl-1-Pentene,-3.03,CCCC(=C)C,[C][C][C][C][=Branch1][C][=C][C],\"InChI=1S/C6H12/c1-4-5-6(2)3/h2,4-5H2,1,3H3\"\n2-Methyl-2-heptanol,-1.72,CCCCCC(C)(C)O,[C][C][C][C][C][C][Branch1][C][C][Branch1][C][C][O],\"InChI=1S/C8H18O/c1-4-5-6-7-8(2,3)9/h9H,4-7H2,1-3H3\"\n2-Methyl-2-hexanol,-1.08,CCCCC(C)(C)O,[C][C][C][C][C][Branch1][C][C][Branch1][C][C][O],\"InChI=1S/C7H16O/c1-4-5-6-7(2,3)8/h8H,4-6H2,1-3H3\"\n2-Methyl-2-pentanol,-0.49,CCCC(C)(C)O,[C][C][C][C][Branch1][C][C][Branch1][C][C][O],\"InChI=1S/C6H14O/c1-4-5-6(2,3)7/h7H,4-5H2,1-3H3\"\n2-Methyl-3-pentanol,-0.7,CCC(O)C(C)C,[C][C][C][Branch1][C][O][C][Branch1][C][C][C],\"InChI=1S/C6H14O/c1-4-6(7)5(2)3/h5-7H,4H2,1-3H3\"\n2-Methylanthracene,-6.96,Cc1ccc2cc3ccccc3cc2c1,[C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C],\"InChI=1S/C15H12/c1-11-6-7-14-9-12-4-2-3-5-13(12)10-15(14)8-11/h2-10H,1H3\"\n2-Methylbutan-2-ol,0.15,CCC(C)(C)O,[C][C][C][Branch1][C][C][Branch1][C][C][O],\"InChI=1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3\"\n2-Methylbutane,-3.18,CCC(C)C,[C][C][C][Branch1][C][C][C],\"InChI=1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3\"\n2-Methylbutanol,-0.47,CCC(C)CO,[C][C][C][Branch1][C][C][C][O],\"InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3\"\n2-Methylheptane,-5.08,CCCCCC(C)C,[C][C][C][C][C][C][Branch1][C][C][C],\"InChI=1S/C8H18/c1-4-5-6-7-8(2)3/h8H,4-7H2,1-3H3\"\n2-Methylnapthalene,-3.77,Cc1ccc2ccccc2c1,[C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"InChI=1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3\"\n2-Methylpentane,-3.74,CCCC(C)C,[C][C][C][C][Branch1][C][C][C],\"InChI=1S/C6H14/c1-4-5-6(2)3/h6H,4-5H2,1-3H3\"\n2-Methylpentanol,-1.11,CCCC(C)CO,[C][C][C][C][Branch1][C][C][C][O],\"InChI=1S/C6H14O/c1-3-4-6(2)5-7/h6-7H,3-5H2,1-2H3\"\n2-Methylphenanthrene,-5.84,Cc1ccc2c(ccc3ccccc32)c1,[C][C][=C][C][=C][C][Branch1][=N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2][=C][Ring1][=C],\"InChI=1S/C15H12/c1-11-6-9-15-13(10-11)8-7-12-4-2-3-5-14(12)15/h2-10H,1H3\"\n2-Methylphenol,-0.62,Cc1ccccc1O,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][O],\"InChI=1S/C7H8O/c1-6-4-2-3-5-7(6)8/h2-5,8H,1H3\"\n2-Methylpropan-1-ol,0.1,CC(C)CO,[C][C][Branch1][C][C][C][O],\"InChI=1S/C4H10O/c1-4(2)3-5/h4-5H,3H2,1-2H3\"\n2-Methylpropane,-2.55,CC(C)C,[C][C][Branch1][C][C][C],\"InChI=1S/C4H10/c1-4(2)3/h4H,1-3H3\"\n2-Methylpropene,-2.33,CC(=C)C,[C][C][=Branch1][C][=C][C],\"InChI=1S/C4H8/c1-4(2)3/h1H2,2-3H3\"\n2-methylpteridine,-0.12,Cc2ncc1nccnc1n2,[C][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"InChI=1S/C7H6N4/c1-5-10-4-6-7(11-5)9-3-2-8-6/h2-4H,1H3\"\n2-Methyltetrahydrofurane,0.11,CC1CCCO1,[C][C][C][C][C][O][Ring1][Branch1],\"InChI=1S/C5H10O/c1-5-3-2-4-6-5/h5H,2-4H2,1H3\"\n2-Napthol,-2.28,Oc1ccc2ccccc2c1,[O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"InChI=1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H\"\n2-Nitropropane,-0.62,CC(C)N(=O)=O,[C][C][Branch1][C][C][N][=Branch1][C][=O][=O],\"InChI=1S/C3H7NO2/c1-3(2)4(5)6/h3H,1-2H3\"\n2-Nonanol,-2.74,CCCCCCCC(C)O,[C][C][C][C][C][C][C][C][Branch1][C][C][O],\"InChI=1S/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3\"\n2-Nonanone,-2.58,CCCCCCCC(=O)C,[C][C][C][C][C][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C9H18O/c1-3-4-5-6-7-8-9(2)10/h3-8H2,1-2H3\"\n2-Octanol,-2.09,CCCCCCC(C)O,[C][C][C][C][C][C][C][Branch1][C][C][O],\"InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3\"\n2-Octanone,-2.05,CCCCCCC(=O)C,[C][C][C][C][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C8H16O/c1-3-4-5-6-7-8(2)9/h3-7H2,1-2H3\"\n2-Pentanol,-0.29,CCCC(C)O,[C][C][C][C][Branch1][C][C][O],\"InChI=1S/C5H12O/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3\"\n2-Pentanone,-0.19,CCCC(=O)C,[C][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C5H10O/c1-3-4-5(2)6/h3-4H2,1-2H3\"\n2-Phenoxyethanol,-0.7,OCCOc1ccccc1,[O][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H10O2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2\"\n2-Propanol,0.43,CC(C)O,[C][C][Branch1][C][C][O],\"InChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3\"\n2-pyrrolidone,1.07,O=C1CCCN1,[O][=C][C][C][C][N][Ring1][Branch1],\"InChI=1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6)\"\n2-Undecanol,-2.94,CCCCCCCCCC(C)O,[C][C][C][C][C][C][C][C][C][C][Branch1][C][C][O],\"InChI=1S/C11H24O/c1-3-4-5-6-7-8-9-10-11(2)12/h11-12H,3-10H2,1-2H3\"\n\"3,3-Dimethyl-1-butanol\",-0.5,CC(C)(C)CCO,[C][C][Branch1][C][C][Branch1][C][C][C][C][O],\"InChI=1S/C6H14O/c1-6(2,3)4-5-7/h7H,4-5H2,1-3H3\"\n\"3,3-Dimethyl-2-butanol\",-0.62,CC(O)C(C)(C)C,[C][C][Branch1][C][O][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C6H14O/c1-5(7)6(2,3)4/h5,7H,1-4H3\"\n\"3,3-Dimethyl-2-butanone\",-0.72,CC(=O)C(C)(C)C,[C][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C6H12O/c1-5(7)6(2,3)4/h1-4H3\"\n\"3,3-Dimethylpentane\",-4.23,CCC(C)(C)CC,[C][C][C][Branch1][C][C][Branch1][C][C][C][C],\"InChI=1S/C7H16/c1-5-7(3,4)6-2/h5-6H2,1-4H3\"\n\"3,4-Dichloronitrobenzene\",-3.2,O=N(=O)c1cc(Cl)c(Cl)cc1,[O][=N][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2],InChI=1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H\n\"3,4-Dichlorophenol\",-1.25,Oc1ccc(Cl)c(Cl)c1,[O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C6H4Cl2O/c7-5-2-1-4(9)3-6(5)8/h1-3,9H\"\n\"3,4-Dimethylphenol\",-1.38,Cc1ccc(O)cc1C,[C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C],\"InChI=1S/C8H10O/c1-6-3-4-8(9)5-7(6)2/h3-5,9H,1-2H3\"\n\"3,4-Dimethylpyridine\",0.36,Cc1ccncc1C,[C][C][=C][C][=N][C][=C][Ring1][=Branch1][C],\"InChI=1S/C7H9N/c1-6-3-4-8-5-7(6)2/h3-5H,1-2H3\"\n\"3,5-Dichlorophenol\",-1.34,Oc1cc(Cl)cc(Cl)c1,[O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C6H4Cl2O/c7-4-1-5(8)3-6(9)2-4/h1-3,9H\"\n\"3,5-Dimethylphenol\",-1.4,Cc1cc(C)cc(O)c1,[C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][O][=C][Ring1][Branch2],\"InChI=1S/C8H10O/c1-6-3-7(2)5-8(9)4-6/h3-5,9H,1-2H3\"\n\"3,5-Dimethylpyridine\",0.38,Cc1cncc(C)c1,[C][C][=C][N][=C][C][Branch1][C][C][=C][Ring1][#Branch1],\"InChI=1S/C7H9N/c1-6-3-7(2)5-8-4-6/h3-5H,1-2H3\"\n3-Butanoyloxymethylphenytoin,-5.071,O=C1N(COC(=O)CCC)C(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][Branch1][#Branch2][C][O][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C20H20N2O4/c1-2-9-17(23)26-14-22-18(24)20(21-19(22)25,15-10-5-3-6-11-15)16-12-7-4-8-13-16/h3-8,10-13H,2,9,14H2,1H3,(H,21,25)\"\n3-Chloroanisole,-2.78,COc1cccc(Cl)c1,[C][O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],\"InChI=1S/C7H7ClO/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3\"\n3-Chlorobiphenyl,-4.88,c1c(Cl)cccc1c2ccccc2,[C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C12H9Cl/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H\n3-Chlorophenol,-0.7,Oc1cccc(Cl)c1,[O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],\"InChI=1S/C6H5ClO/c7-5-2-1-3-6(8)4-5/h1-4,8H\"\n3-Ethanoyloxymethylphenytoin,-4.47,O=C1N(COC(=O)C)C(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C18H16N2O4/c1-13(21)24-12-20-16(22)18(19-17(20)23,14-8-4-2-5-9-14)15-10-6-3-7-11-15/h2-11H,12H2,1H3,(H,19,23)\"\n3-Ethyl-3-pentanol,-0.85,CCC(O)(CC)CC,[C][C][C][Branch1][C][O][Branch1][Ring1][C][C][C][C],\"InChI=1S/C7H16O/c1-4-7(8,5-2)6-3/h8H,4-6H2,1-3H3\"\n3-Heptanol ,-1.47,CCCCC(O)CC,[C][C][C][C][C][Branch1][C][O][C][C],\"InChI=1S/C7H16O/c1-3-5-6-7(8)4-2/h7-8H,3-6H2,1-2H3\"\n3-Heptanoyloxymethylphenytoin,-6.301,O=C1N(COC(=O)CCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][Branch1][=N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C23H26N2O4/c1-2-3-4-11-16-20(26)29-17-25-21(27)23(24-22(25)28,18-12-7-5-8-13-18)19-14-9-6-10-15-19/h5-10,12-15H,2-4,11,16-17H2,1H3,(H,24,28)\"\n3-Hexanol,-0.8,CCCC(O)CC,[C][C][C][C][Branch1][C][O][C][C],\"InChI=1S/C6H14O/c1-3-5-6(7)4-2/h6-7H,3-5H2,1-2H3\"\n3-Hexanone,-0.83,CCCC(=O)CC,[C][C][C][C][=Branch1][C][=O][C][C],\"InChI=1S/C6H12O/c1-3-5-6(7)4-2/h3-5H2,1-2H3\"\n3-Hexanoyloxymethylphenyltoin,-5.886,O=C1N(COC(=O)CCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][Branch1][N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][#C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C22H24N2O4/c1-2-3-6-15-19(25)28-16-24-20(26)22(23-21(24)27,17-11-7-4-8-12-17)18-13-9-5-10-14-18/h4-5,7-14H,2-3,6,15-16H2,1H3,(H,23,27)\"\n3-Hexyne,-1.99,CCC#CCC,[C][C][C][#C][C][C],\"InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H2,1-2H3\"\n3-Methyl-1-Butene,-2.73,CC(C)C=C,[C][C][Branch1][C][C][C][=C],\"InChI=1S/C5H10/c1-4-5(2)3/h4-5H,1H2,2-3H3\"\n3-Methyl-2-butanol,-0.18,CC(C)C(C)O,[C][C][Branch1][C][C][C][Branch1][C][C][O],\"InChI=1S/C5H12O/c1-4(2)5(3)6/h4-6H,1-3H3\"\n3-Methyl-2-butanone,-0.12,CC(C)C(=O)C,[C][C][Branch1][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3\"\n3-Methyl-2-pentanol,-0.72,CCC(C)CCO,[C][C][C][Branch1][C][C][C][C][O],\"InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\"\n3-Methyl-2-pentanol,-0.71,CCC(C)CCO,[C][C][C][Branch1][C][C][C][C][O],\"InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\"\n3-Methyl-2-pentanone,-0.67,CCC(C)C(=O)C,[C][C][C][Branch1][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C6H12O/c1-4-5(2)6(3)7/h5H,4H2,1-3H3\"\n3-Methyl-3-heptanol,-1.6,CCCCC(C)(O)CC,[C][C][C][C][C][Branch1][C][C][Branch1][C][O][C][C],\"InChI=1S/C8H18O/c1-4-6-7-8(3,9)5-2/h9H,4-7H2,1-3H3\"\n3-Methyl-3-hexanol,-0.98,CCCC(C)(O)CC,[C][C][C][C][Branch1][C][C][Branch1][C][O][C][C],\"InChI=1S/C7H16O/c1-4-6-7(3,8)5-2/h8H,4-6H2,1-3H3\"\n3-Methyl-3-pentanol,-0.36,CCC(C)(O)CC,[C][C][C][Branch1][C][C][Branch1][C][O][C][C],\"InChI=1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3\"\n3-Methylbutan-1-ol,-0.51,CC(C)CCO,[C][C][Branch1][C][C][C][C][O],\"InChI=1S/C5H12O/c1-5(2)3-4-6/h5-6H,3-4H2,1-2H3\"\n3-Methylcholanthrene,-7.92,c1cc(C)cc2c1c3cc4cccc5CCc(c45)c3cc2,[C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][C][C][C][Branch1][=Branch1][C][Ring1][=Branch2][=Ring1][Branch1][=C][Ring1][N][C][=C][Ring1][S],\"InChI=1S/C21H16/c1-13-5-8-17-15(11-13)7-9-18-19-10-6-14-3-2-4-16(21(14)19)12-20(17)18/h2-5,7-9,11-12H,6,10H2,1H3\"\n3-Methylheptane,-5.16,CCCCC(C)CC,[C][C][C][C][C][Branch1][C][C][C][C],\"InChI=1S/C8H18/c1-4-6-7-8(3)5-2/h8H,4-7H2,1-3H3\"\n3-Methylpentane,-3.68,CCC(C)CC,[C][C][C][Branch1][C][C][C][C],\"InChI=1S/C6H14/c1-4-6(3)5-2/h6H,4-5H2,1-3H3\"\n3-Methylphenol,-0.68,Cc1cccc(O)c1,[C][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1],\"InChI=1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3\"\n3-Octanol,-1.98,CCCCCC(O)CC,[C][C][C][C][C][C][Branch1][C][O][C][C],\"InChI=1S/C8H18O/c1-3-5-6-7-8(9)4-2/h8-9H,3-7H2,1-2H3\"\n3-Octanoyloxymethylphenytoin,-6.523,O=C1N(COC(=O)CCCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][Branch1][=C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][P][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C24H28N2O4/c1-2-3-4-5-12-17-21(27)30-18-26-22(28)24(25-23(26)29,19-13-8-6-9-14-19)20-15-10-7-11-16-20/h6-11,13-16H,2-5,12,17-18H2,1H3,(H,25,29)\"\n3-Pentanol,-0.24,CCC(O)CC,[C][C][C][Branch1][C][O][C][C],\"InChI=1S/C5H12O/c1-3-5(6)4-2/h5-6H,3-4H2,1-2H3\"\n3-Pentanone,-0.28,CCC(=O)CC,[C][C][C][=Branch1][C][=O][C][C],\"InChI=1S/C5H10O/c1-3-5(6)4-2/h3-4H2,1-2H3\"\n3-Pentanoyloxymethylphenytoin,-4.678,O=C1N(COC(=O)CCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][Branch1][O][C][O][C][=Branch1][C][=O][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C21H22N2O4/c1-2-3-14-18(24)27-15-23-19(25)21(22-20(23)26,16-10-6-4-7-11-16)17-12-8-5-9-13-17/h4-13H,2-3,14-15H2,1H3,(H,22,26)\"\n3-Propanoyloxymethylphenytoin,-4.907,O=C1N(COC(=O)CC)C(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][Branch1][=Branch2][C][O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C19H18N2O4/c1-2-16(22)25-13-21-17(23)19(20-18(21)24,14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-12H,2,13H2,1H3,(H,20,24)\"\n4-Bromophenol,-1.09,Oc1ccc(Br)cc1,[O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],\"InChI=1S/C6H5BrO/c7-5-1-3-6(8)4-2-5/h1-4,8H\"\n4-Bromotoluene,-3.19,Cc1ccc(Br)cc1,[C][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],\"InChI=1S/C7H7Br/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\"\n4-Chloroanisole,-2.78,COc1ccc(Cl)cc1,[C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C7H7ClO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3\"\n4-Chlorophenol ,-0.7,Oc1ccc(Cl)cc1,[O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C6H5ClO/c7-5-1-3-6(8)4-2-5/h1-4,8H\"\n4-Chlorotoluene,-3.08,Cc1ccc(Cl)cc1,[C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C7H7Cl/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\"\n4-Ethyltoluene,-3.11,CCc1ccc(C)cc1,[C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],\"InChI=1S/C9H12/c1-3-9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3\"\n4-Heptanol,-1.4,CCCC(O)CCC,[C][C][C][C][Branch1][C][O][C][C][C],\"InChI=1S/C7H16O/c1-3-5-7(8)6-4-2/h7-8H,3-6H2,1-2H3\"\n4-Heptanone,-1.3,CCCC(=O)CCC,[C][C][C][C][=Branch1][C][=O][C][C][C],\"InChI=1S/C7H14O/c1-3-5-7(8)6-4-2/h3-6H2,1-2H3\"\n4-hexylresorcinol,-2.59,c1(O)cc(O)ccc1CCCCCC,[C][Branch1][C][O][=C][C][Branch1][C][O][=C][C][=C][Ring1][Branch2][C][C][C][C][C][C],\"InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3\"\n4-hydroxypyridine,1.02,Oc1ccncc1,[O][C][=C][C][=N][C][=C][Ring1][=Branch1],\"InChI=1S/C5H5NO/c7-5-1-3-6-4-2-5/h1-4H,(H,6,7)\"\n4-Isopropyltoluene,-3.77,CC(C)c1ccc(C)cc1,[C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],\"InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H3\"\n4-Methyl-2-pentanol,-0.8,CC(C)CC(C)O,[C][C][Branch1][C][C][C][C][Branch1][C][C][O],\"InChI=1S/C6H14O/c1-5(2)4-6(3)7/h5-7H,4H2,1-3H3\"\n4-Methyl-2-pentanone,-0.74,CC(C)CC(=O)C,[C][C][Branch1][C][C][C][C][=Branch1][C][=O][C],\"InChI=1S/C6H12O/c1-5(2)4-6(3)7/h5H,4H2,1-3H3\"\n4-Methylbiphenyl,-4.62,Cc1ccc(cc1)c2ccccc2,[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C13H12/c1-11-7-9-13(10-8-11)12-5-3-2-4-6-12/h2-10H,1H3\"\n4-Methylpentanol,-1.14,CC(C)CCCO,[C][C][Branch1][C][C][C][C][C][O],\"InChI=1S/C6H14O/c1-6(2)4-3-5-7/h6-7H,3-5H2,1-2H3\"\n4-methylpteridine,-0.466,Cc1ncnc2nccnc12,[C][C][=N][C][=N][C][=N][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1],\"InChI=1S/C7H6N4/c1-5-6-7(11-4-10-5)9-3-2-8-6/h2-4H,1H3\"\n4-Nitroacetanilide,-2.692,CC(=O)Nc1ccc(cc1)N(=O)=O,[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)\"\n4-Pentene-1-ol,-0.15,OCCCC=C,[O][C][C][C][C][=C],\"InChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2\"\n5-(3-Methyl-2-butenyl)-5-ethylbarbital,-2.253,O=C1NC(=O)NC(=O)C1(CC)CC=C(C)C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C][Branch1][C][C][C],\"InChI=1S/C11H16N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h5H,4,6H2,1-3H3,(H2,12,13,14,15,16)\"\n5-(3-Methyl-2-butenyl)-5-isoPrbarbital,-2.593,O=C1NC(=O)NC(=O)C1(C(C)C)CC=C(C)C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C][Branch1][C][C][C],\"InChI=1S/C12H18N2O3/c1-7(2)5-6-12(8(3)4)9(15)13-11(17)14-10(12)16/h5,8H,6H2,1-4H3,(H2,13,14,15,16,17)\"\n\"5,5-Diallylbarbital\",-2.077,O=C1NC(=O)NC(=O)C1(CC=C)CC=C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][C][=C],\"InChI=1S/C10H12N2O3/c1-3-5-10(6-4-2)7(13)11-9(15)12-8(10)14/h3-4H,1-2,5-6H2,(H2,11,12,13,14,15)\"\n\"5,5-Diisopropylbarbital\",-2.766,O=C1NC(=O)NC(=O)C1(C(C)C)C(C)C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][Branch1][C][C][C],\"InChI=1S/C10H16N2O3/c1-5(2)10(6(3)4)7(13)11-9(15)12-8(10)14/h5-6H,1-4H3,(H2,11,12,13,14,15)\"\n\"5,5-Dimethylbarbituric acid\",-1.742,O=C1NC(=O)NC(=O)C1(C)C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C],\"InChI=1S/C6H8N2O3/c1-6(2)3(9)7-5(11)8-4(6)10/h1-2H3,(H2,7,8,9,10,11)\"\n\"5,6-Dimethylchrysene\",-7.01,Cc1c(C)c2c3ccccc3ccc2c4ccccc14,[C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1],\"InChI=1S/C20H16/c1-13-14(2)20-17-9-4-3-7-15(17)11-12-19(20)18-10-6-5-8-16(13)18/h3-12H,1-2H3\"\n5-Allyl-5-ethylbarbital,-1.614,O=C1NC(=O)NC(=O)C1(CC)CC=C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C],\"InChI=1S/C9H12N2O3/c1-3-5-9(4-2)6(12)10-8(14)11-7(9)13/h3H,1,4-5H2,2H3,(H2,10,11,12,13,14)\"\n5-Allyl-5-isopropylbarbital,-1.708,O=C1NC(=O)NC(=O)C1(C(C)C)CC=C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C],\"InChI=1S/C10H14N2O3/c1-4-5-10(6(2)3)7(13)11-9(15)12-8(10)14/h4,6H,1,5H2,2-3H3,(H2,11,12,13,14,15)\"\n5-Allyl-5-methylbarbital,-1.16,O=C1NC(=O)NC(=O)C1(C)CC=C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C][=C],\"InChI=1S/C8H10N2O3/c1-3-4-8(2)5(11)9-7(13)10-6(8)12/h3H,1,4H2,2H3,(H2,9,10,11,12,13)\"\n5-Allyl-5-phenylbarbital,-2.369,O=C1NC(=O)NC(=O)C1(CC=C)c1ccccc1,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C13H12N2O3/c1-2-8-13(9-6-4-3-5-7-9)10(16)14-12(18)15-11(13)17/h2-7H,1,8H2,(H2,14,15,16,17,18)\"\n5-Ethyl-5-(3-methylbutyl)barbital,-2.658,O=C1NC(=O)NC(=O)C1(CC)CCC(C)C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][C][Branch1][C][C][C],\"InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\"\n5-Ethyl-5-isopropylbarbituric acid,-2.148,O=C1NC(=O)NC(=O)C1(CC)C(C)C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C],\"InChI=1S/C9H14N2O3/c1-4-9(5(2)3)6(12)10-8(14)11-7(9)13/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\"\n5-Ethyl-5-phenylbarbital,-2.322,O=C1NC(=O)NC(=O)C1(CC)c1ccccc1,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17)\"\n5-Methyl-5-ethylbarbituric acid,-1.228,O=C1NC(=O)NC(=O)C1(C)CC,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C],\"InChI=1S/C7H10N2O3/c1-3-7(2)4(10)8-6(12)9-5(7)11/h3H2,1-2H3,(H2,8,9,10,11,12)\"\n5-Methylchrysene,-6.59,c1cccc2c3c(C)cc4ccccc4c3ccc12,[C][=C][C][=C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#C],\"InChI=1S/C19H14/c1-13-12-15-7-3-4-8-16(15)18-11-10-14-6-2-5-9-17(14)19(13)18/h2-12H,1H3\"\n5-Nonanone,-2.58,CCCCC(=O)CCCC,[C][C][C][C][C][=Branch1][C][=O][C][C][C][C],\"InChI=1S/C9H18O/c1-3-5-7-9(10)8-6-4-2/h3-8H2,1-2H3\"\n6-methoxypteridine,-1.139,COc2cnc1ncncc1n2,[C][O][C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"InChI=1S/C7H6N4O/c1-12-6-3-9-7-5(11-6)2-8-4-10-7/h2-4H,1H3\"\n6-Methylchrysene,-6.57,Cc1cc2c3ccccc3ccc2c4ccccc14,[C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1],\"InChI=1S/C19H14/c1-13-12-19-16-8-3-2-6-14(16)10-11-18(19)17-9-5-4-7-15(13)17/h2-12H,1H3\"\n\"7,12-Dimethylbenz(a)anthracene\",-7.02,Cc1c2ccccc2c(C)c3ccc4ccccc4c13,[C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring2][Ring1][Ring1][Ring1][#Branch2],\"InChI=1S/C20H16/c1-13-16-8-5-6-9-17(16)14(2)20-18(13)12-11-15-7-3-4-10-19(15)20/h3-12H,1-2H3\"\n7-methoxypteridine,-0.91,COc2cnc1cncnc1n2,[C][O][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"InChI=1S/C7H6N4O/c1-12-6-3-9-5-2-8-4-10-7(5)11-6/h2-4H,1H3\"\n7-methylpteridine,-0.854,Cc2cnc1cncnc1n2,[C][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"InChI=1S/C7H6N4/c1-5-2-9-6-3-8-4-10-7(6)11-5/h2-4H,1H3\"\n\"9,10-Dimethylanthracene\",-6.57,Cc1c2ccccc2c(C)c3ccccc13,[C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"InChI=1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3\"\n9-Methylanthracene,-5.89,Cc1c2ccccc2cc3ccccc13,[C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1],\"InChI=1S/C15H12/c1-11-14-8-4-2-6-12(14)10-13-7-3-5-9-15(11)13/h2-10H,1H3\"\nAbate,-6.237,COP(=S)(OC)Oc1ccc(Sc2ccc(OP(=S)(OC)OC)cc2)cc1,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][S][C][=C][C][=C][Branch1][N][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=C][Ring1][=N][C][=C][Ring2][Ring1][Ring2],\"InChI=1S/C16H20O6P2S3/c1-17-23(25,18-2)21-13-5-9-15(10-6-13)27-16-11-7-14(8-12-16)22-24(26,19-3)20-4/h5-12H,1-4H3\"\nAcenapthene,-4.63,C1Cc2cccc3cccc1c23,[C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1],\"InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2\"\nAcenapthylene,-3.96,C1=Cc2cccc3cccc1c23,[C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H\nAcetamide,1.58,CC(=O)N,[C][C][=Branch1][C][=O][N],\"InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)\"\nAcetanilide,-1.33,CC(=O)Nc1ccccc1,[C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)\"\nAcetonitrile,0.26,CC#N,[C][C][#N],InChI=1S/C2H3N/c1-2-3/h1H3\nAcetophenone,-1.28,CC(=O)c1ccccc1,[C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3\"\nAcridine,-3.67,c3ccc2nc1ccccc1cc2c3,[C][=C][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C],InChI=1S/C13H9N/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-9H\nAcrolein,0.57,C=CC=O,[C][=C][C][=O],\"InChI=1S/C3H4O/c1-2-3-4/h2-3H,1H2\"\nAcrylonitrile,0.15,C=CC#N,[C][=C][C][#N],\"InChI=1S/C3H3N/c1-2-3-4/h2H,1H2\"\nAldrin,-6.307,ClC1=C(Cl)C2(Cl)C3C4CC(C=C4)C3C1(Cl)C2(Cl)Cl,[Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch1][C][=C][Ring1][Branch1][C][Ring1][#Branch1][C][Ring1][=N][Branch1][C][Cl][C][Ring1][N][Branch1][C][Cl][Cl],\"InChI=1S/C12H8Cl6/c13-8-9(14)11(16)7-5-2-1-4(3-5)6(7)10(8,15)12(11,17)18/h1-2,4-7H,3H2\"\nallicin,-0.83,C=CCS(=O)SCC=C,[C][=C][C][S][=Branch1][C][=O][S][C][C][=C],\"InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2\"\nalloxantin,-1.99,C1(=O)NC(=O)NC(=O)C1(O)C2(O)C(=O)NC(=O)NC2(=O),[C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][=Branch2][Branch1][C][O][C][Branch1][C][O][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=Branch2][=O],\"InChI=1S/C8H6N4O8/c13-1-7(19,2(14)10-5(17)9-1)8(20)3(15)11-6(18)12-4(8)16/h19-20H,(H2,9,10,13,14,17)(H2,11,12,15,16,18)\"\nAltretamine,-3.364,CN(C)c1nc(nc(n1)N(C)C)N(C)C,[C][N][Branch1][C][C][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C],InChI=1S/C9H18N6/c1-13(2)7-10-8(14(3)4)12-9(11-7)15(5)6/h1-6H3\nAmetryn,-3.04,CCNc1nc(NC(C)C)nc(SC)n1,[C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N],\"InChI=1S/C9H17N5S/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\"\nAminocarb,-2.36,CNC(=O)Oc1ccc(N(C)C)c(C)c1,[C][N][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][=Branch1][N][Branch1][C][C][C][C][Branch1][C][C][=C][Ring1][#Branch2],\"InChI=1S/C11H16N2O2/c1-8-7-9(15-11(14)12-2)5-6-10(8)13(3)4/h5-7H,1-4H3,(H,12,14)\"\nAmitraz,-5.47,CN(C=Nc1ccc(C)cc1C)C=Nc2ccc(C)cc2C,[C][N][Branch1][#C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C],\"InChI=1S/C19H23N3/c1-14-6-8-18(16(3)10-14)20-12-22(5)13-21-19-9-7-15(2)11-17(19)4/h6-13H,1-5H3\"\nAmitrole,0.522,Nc1nc[nH]n1,[N][C][N][=C][NH1][N][=Ring1][Branch1],\"InChI=1S/C2H4N4/c3-2-4-1-5-6-2/h1H,(H3,3,4,5,6)\"\nAmobarbital,-2.468,CCC1(CCC(C)C)C(=O)NC(=O)NC1=O,[C][C][C][Branch1][Branch2][C][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=N][=O],\"InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\"\nampyrone,-0.624,Cc2c(N)c(=O)n(c1ccccc1)n2C,[C][C][=C][Branch1][C][N][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=N][C],\"InChI=1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3\"\nAndrostenedione,-3.69,CC34CCC1C(CCC2=CC(=O)CCC12C)C3CCC4=O,[C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O],\"InChI=1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-16H,3-10H2,1-2H3\"\nAndrosterone,-4.402,CC12CCC(O)CC1CCC3C2CCC4(C)C3CCC4=O,[C][C][C][C][C][Branch1][C][O][C][C][Ring1][#Branch1][C][C][C][C][Ring1][O][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][=O],\"InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\"\nAnethole,-3.13,COc1ccc(C=CC)cc1,[C][O][C][=C][C][=C][Branch1][Ring2][C][=C][C][C][=C][Ring1][=Branch2],\"InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3-8H,1-2H3\"\nAniline ,-0.41,Nc1ccccc1,[N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2\"\nAnilofos,-4.432,COP(=S)(OC)SCC(=O)N(C(C)C)c1ccc(Cl)cc1,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C13H19ClNO3PS2/c1-10(2)15(12-7-5-11(14)6-8-12)13(16)9-21-19(20,17-3)18-4/h5-8,10H,9H2,1-4H3\"\nAnisole,-1.85,COc1ccccc1,[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\"\nAnthracene,-6.35,c1ccc2cc3ccccc3cc2c1,[C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C],InChI=1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H\nAnthraquinone,-5.19,O=C1c2ccccc2C(=O)c3ccccc13,[O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],InChI=1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H\nAntipyrene,0.715,Cc1cc(=O)n(c2ccccc2)n1C,[C][C][=C][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][N][C],\"InChI=1S/C11H12N2O/c1-9-8-11(14)13(12(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3\"\n\"Atovaquone(0,430mg/ml) - neutral\",-5.931,OC4=C(C1CCC(CC1)c2ccc(Cl)cc2)C(=O)c3ccccc3C4=O,[O][C][=C][Branch2][Ring1][=Branch1][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][Branch2][=O],\"InChI=1S/C22H19ClO3/c23-16-11-9-14(10-12-16)13-5-7-15(8-6-13)19-20(24)17-3-1-2-4-18(17)21(25)22(19)26/h1-4,9-13,15,26H,5-8H2\"\nAtratone,-2.084,CCNc1nc(NC(C)C)nc(OC)n1,[C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][N],\"InChI=1S/C9H17N5O/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\"\nAtrazine,-3.85,CCNc1nc(Cl)nc(NC(C)C)n1,[C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O],\"InChI=1S/C8H14ClN5/c1-4-10-7-12-6(9)13-8(14-7)11-5(2)3/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\"\nAzintamide,-1.716,CCN(CC)C(=O)CSc1ccc(Cl)nn1,[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][S][C][=C][C][=C][Branch1][C][Cl][N][=N][Ring1][#Branch1],\"InChI=1S/C10H14ClN3OS/c1-3-14(4-2)10(15)7-16-9-6-5-8(11)12-13-9/h5-6H,3-4,7H2,1-2H3\"\nAzobenzene,-4.45,N(=Nc1ccccc1)c2ccccc2,[N][=Branch1][#Branch2][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C12H10N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H\nAzodrin,0.651,CNC(=O)C=C(C)OP(=O)(OC)OC,[C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C],\"InChI=1S/C7H14NO5P/c1-6(5-7(9)8-2)13-14(10,11-3)12-4/h5H,1-4H3,(H,8,9)\"\nBarban,-4.37,ClCC#CCOC(=O)Nc1cccc(Cl)c1,[Cl][C][C][#C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],\"InChI=1S/C11H9Cl2NO2/c12-6-1-2-7-16-11(15)14-10-5-3-4-9(13)8-10/h3-5,8H,6-7H2,(H,14,15)\"\nBarbital,-2.4,O=C1NC(=O)NC(=O)C1(CC)CC,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C],\"InChI=1S/C8H12N2O3/c1-3-8(4-2)5(11)9-7(13)10-6(8)12/h3-4H2,1-2H3,(H2,9,10,11,12,13)\"\nBendroflumethiazide,-3.59,NS(=O)(=O)c3cc2c(NC(Cc1ccccc1)NS2(=O)=O)cc3C(F)(F)F,[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch1][N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][Ring1][=N][=Branch1][C][=O][=O][C][=C][Ring2][Ring1][Ring1][C][Branch1][C][F][Branch1][C][F][F],\"InChI=1S/C15H14F3N3O4S2/c16-15(17,18)10-7-11-13(8-12(10)26(19,22)23)27(24,25)21-14(20-11)6-9-4-2-1-3-5-9/h1-5,7-8,14,20-21H,6H2,(H2,19,22,23)\"\nBenfluralin,-5.53,CCCCN(CC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O,[C][C][C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O],\"InChI=1S/C13H16F3N3O4/c1-3-5-6-17(4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\"\nBenfuracarb,-4.71,CCOC(=O)CCN(SN(C)C(=O)Oc1cccc2CC(C)(C)Oc21)C(C)C,[C][C][O][C][=Branch1][C][=O][C][C][N][Branch2][Ring1][=C][S][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][=Ring1][#Branch1][Ring1][O][C][Branch1][C][C][C],\"InChI=1S/C20H30N2O5S/c1-7-25-17(23)11-12-22(14(2)3)28-21(6)19(24)26-16-10-8-9-15-13-20(4,5)27-18(15)16/h8-10,14H,7,11-13H2,1-6H3\"\nbenodanil,-4.21,c1c(NC(=O)c2ccccc2(I))cccc1,[C][=C][Branch1][#C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][I][C][=C][C][=C][Ring1][S],\"InChI=1S/C13H10INO/c14-12-9-5-4-8-11(12)13(16)15-10-6-2-1-3-7-10/h1-9H,(H,15,16)\"\nBenomyl,-4.883,CCCCNC(=O)n1c(NC(=O)OC)nc2ccccc12,[C][C][C][C][N][C][=Branch1][C][=O][N][C][Branch1][Branch2][N][C][=Branch1][C][=O][O][C][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1],\"InChI=1S/C14H18N4O3/c1-3-4-9-15-13(19)18-11-8-6-5-7-10(11)16-12(18)17-14(20)21-2/h5-8H,3-4,9H2,1-2H3,(H,15,19)(H,16,17,20)\"\nBensulide,-4.2,CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)c1ccccc1,[C][C][Branch1][C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][O][C][Branch1][C][C][C][S][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C14H24NO4PS3/c1-12(2)18-20(21,19-13(3)4)22-11-10-15-23(16,17)14-8-6-5-7-9-14/h5-9,12-13,15H,10-11H2,1-4H3\"\nBenzaldehyde,-1.19,O=Cc1ccccc1,[O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H\nBenzamide,-0.96,NC(=O)c1ccccc1,[N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)\"\nBenzene ,-1.64,c1ccccc1,[C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H\nbenzhydrol,-2.55,c1ccccc1C(O)c2ccccc2,[C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H\"\nBenznidazole,-2.81,O=C(Cn1ccnc1N(=O)=O)NCc2ccccc2,[O][=C][Branch1][=C][C][N][C][=C][N][=C][Ring1][Branch1][N][=Branch1][C][=O][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H12N4O3/c17-11(14-8-10-4-2-1-3-5-10)9-15-7-6-13-12(15)16(18)19/h1-7H,8-9H2,(H,14,17)\"\nBenzo(a)fluorene,-6.68,C1c2ccccc2c3ccc4ccccc4c13,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][P][Ring1][#Branch2],\"InChI=1S/C17H12/c1-3-7-14-12(5-1)9-10-16-15-8-4-2-6-13(15)11-17(14)16/h1-10H,11H2\"\nBenzo(a)pyrene,-8.699,c1ccc2c(c1)cc3ccc4cccc5ccc2c3c45,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C20H12/c1-2-7-17-15(4-1)12-16-9-8-13-5-3-6-14-10-11-18(17)20(16)19(13)14/h1-12H\nBenzo(b)fluoranthene,-8.23,c1ccc2c(c1)c3cccc4c3c2cc5ccccc54,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2],InChI=1S/C20H12/c1-2-7-14-13(6-1)12-19-16-9-4-3-8-15(16)18-11-5-10-17(14)20(18)19/h1-12H\nBenzo(b)fluorene,-8.04,C1c2ccccc2c3cc4ccccc4cc13,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][P][Ring1][#Branch2],\"InChI=1S/C17H12/c1-2-6-13-11-17-15(9-12(13)5-1)10-14-7-3-4-8-16(14)17/h1-9,11H,10H2\"\nBenzo(e)pyrene,-7.8,c1ccc2c(c1)c3cccc4ccc5cccc2c5c43,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][=Branch1][=C][Ring1][#Branch2][Ring1][=C],InChI=1S/C20H12/c1-2-8-16-15(7-1)17-9-3-5-13-11-12-14-6-4-10-18(16)20(14)19(13)17/h1-12H\nBenzo(j)fluoranthene,-8,c1ccc2c3c(ccc2c1)c4cccc5cccc3c45,[C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][C][Ring1][#C][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C20H12/c1-2-8-15-13(5-1)11-12-17-16-9-3-6-14-7-4-10-18(19(14)16)20(15)17/h1-12H\nBenzo(k)fluoranthene,-8.49,c1ccc2cc3c4cccc5cccc(c3cc2c1)c45,[C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Branch1][N][C][Ring1][O][=C][C][Ring1][#C][=C][Ring2][Ring1][Ring1][=C][Ring1][=C][Ring1][#Branch2],InChI=1S/C20H12/c1-2-6-15-12-19-17-10-4-8-13-7-3-9-16(20(13)17)18(19)11-14(15)5-1/h1-12H\nBenzo[ghi]perylene,-9.018,c1cc2ccc3ccc4ccc5cccc6c(c1)c2c3c4c56,[C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=C][Ring1][#C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1],InChI=1S/C22H12/c1-3-13-7-9-15-11-12-16-10-8-14-4-2-6-18-17(5-1)19(13)21(15)22(16)20(14)18/h1-12H\nBenzocaine,-2.616,CCOC(=O)c1ccc(N)cc1,[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\"\nbenzoin,-2.85,OC(C(=O)c1ccccc1)c2ccccc2,[O][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H\"\nBenzonitrile,-1,N#Cc1ccccc1,[N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H\nBenzophenone,-3.12,O=C(c1ccccc1)c2ccccc2,[O][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H\nBenzotriazole,-0.78,c2ccc1[nH]nnc1c2,[C][=C][C][=C][NH1][N][=N][C][Ring1][Branch1][=C][Ring1][=Branch2],\"InChI=1S/C6H5N3/c1-2-4-6-5(3-1)7-9-8-6/h1-4H,(H,7,8,9)\"\nBenzoxazole,-1.16,c2ccc1ocnc1c2,[C][=C][C][=C][O][C][=N][C][Ring1][Branch1][=C][Ring1][=Branch2],InChI=1S/C7H5NO/c1-2-4-7-6(3-1)8-5-9-7/h1-5H\nBenzylchloride,-2.39,ClCc1ccccc1,[Cl][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H7Cl/c8-6-7-4-2-1-3-5-7/h1-5H,6H2\"\nBenzyltrifluoride,-2.51,FC(F)(F)c1ccccc1,[F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H\"\nBetamethasone-17-valerate,-4.71,CCCCC(=O)OC3(C(C)CC4C2CCC1=CC(=O)C=CC1(C)C2(F)C(O)CC34C)C(=O)CO,[C][C][C][C][C][=Branch1][C][=O][O][C][Branch2][Ring2][O][C][Branch1][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][=Branch1][Ring2][Ring1][C][C][C][=Branch1][C][=O][C][O],\"InChI=1S/C27H37FO6/c1-5-6-7-23(33)34-27(22(32)15-29)16(2)12-20-19-9-8-17-13-18(30)10-11-24(17,3)26(19,28)21(31)14-25(20,27)4/h10-11,13,16,19-21,29,31H,5-9,12,14-15H2,1-4H3\"\nBibenzyl ,-4.62,C(Cc1ccccc1)c2ccccc2,[C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2\"\nBiphenyl,-4.345,c1ccc(cc1)c2ccccc2,[C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C12H10/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-10H\nborneol,-2.32,CC1(C)C2CCC1(C)C(O)C2,[C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][Branch1][C][O][C][Ring1][Branch2],\"InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3\"\nBromobenzene,-2.55,Brc1ccccc1,[Br][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H\nBromochloromethane,-0.89,ClCBr,[Cl][C][Br],InChI=1S/CH2BrCl/c2-1-3/h1H2\nBromodichloromethane,-1.54,BrC(Cl)Cl,[Br][C][Branch1][C][Cl][Cl],InChI=1S/CHBrCl2/c2-1(3)4/h1H\nBromoethane,-1.09,CCBr,[C][C][Br],\"InChI=1S/C2H5Br/c1-2-3/h2H2,1H3\"\nBromomethane,-0.79,CBr,[C][Br],InChI=1S/CH3Br/c1-2/h1H3\nBromophos,-6.09,COP(=S)(OC)Oc1cc(Cl)c(Br)cc1Cl,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Cl],\"InChI=1S/C8H8BrCl2O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\"\nbrompyrazone,-3.127,c1ccccc1n2ncc(N)c(Br)c2(=O),[C][=C][C][=C][C][=C][Ring1][=Branch1][N][N][=C][C][Branch1][C][N][=C][Branch1][C][Br][C][Ring1][Branch2][=O],\"InChI=1S/C10H8BrN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\"\nButabarbital,-2.39,O=C1NC(=O)NC(=O)C1(CC)C(C)CC,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C],\"InChI=1S/C10H16N2O3/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15)\"\nbutacarb,-4.24,c1(C(C)(C)C)cc(C(C)(C)C)cc(OC(=O)NC)c1,[C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][Branch2][O][C][=Branch1][C][=O][N][C][=C][Ring2][Ring1][Ring1],\"InChI=1S/C16H25NO2/c1-15(2,3)11-8-12(16(4,5)6)10-13(9-11)19-14(18)17-7/h8-10H,1-7H3,(H,17,18)\"\nButamben,-3.082,CCCCOC(=O)c1ccc(N)cc1,[C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C11H15NO2/c1-2-3-8-14-11(13)9-4-6-10(12)7-5-9/h4-7H,2-3,8,12H2,1H3\"\nButan-2-ol,0.47,CCC(C)O,[C][C][C][Branch1][C][C][O],\"InChI=1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3\"\nButane,-2.57,CCCC,[C][C][C][C],\"InChI=1S/C4H10/c1-3-4-2/h3-4H2,1-2H3\"\nButanethiol ,-2.18,CCCCS,[C][C][C][C][S],\"InChI=1S/C4H10S/c1-2-3-4-5/h5H,2-4H2,1H3\"\nButethal,-1.661,CCCCC1(CC)C(=O)NC(=O)NC1=O,[C][C][C][C][C][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][#Branch2][=O],\"InChI=1S/C10H16N2O3/c1-3-5-6-10(4-2)7(13)11-9(15)12-8(10)14/h3-6H2,1-2H3,(H2,11,12,13,14,15)\"\nButhidazole,-1.877,CN1CC(O)N(C1=O)c2nnc(s2)C(C)(C)C,[C][N][C][C][Branch1][C][O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C10H16N4O2S/c1-10(2,3)7-11-12-8(17-7)14-6(15)5-13(4)9(14)16/h6,15H,5H2,1-4H3\"\nButuron,-3.9,CC(C#C)N(C)C(=O)Nc1ccc(Cl)cc1,[C][C][Branch1][Ring1][C][#C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C12H13ClN2O/c1-4-9(2)15(3)12(16)14-11-7-5-10(13)6-8-11/h1,5-9H,2-3H3,(H,14,16)\"\nButyl acetate,-1.37,CCCCOC=O,[C][C][C][C][O][C][=O],\"InChI=1S/C5H10O2/c1-2-3-4-7-5-6/h5H,2-4H2,1H3\"\nButylate,-3.68,CCSC(=O)N(CC(C)C)CC(C)C,[C][C][S][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][C][Branch1][C][C][C],\"InChI=1S/C11H23NOS/c1-6-14-11(13)12(7-9(2)3)8-10(4)5/h9-10H,6-8H2,1-5H3\"\nButylbenzene,-4.06,CCCCc1ccccc1,[C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C10H14/c1-2-3-7-10-8-5-4-6-9-10/h4-6,8-9H,2-3,7H2,1H3\"\nButyraldehyde,-0.01,CCCC=O,[C][C][C][C][=O],\"InChI=1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3\"\nCaffeine,-0.876,Cn1cnc2n(C)c(=O)n(C)c(=O)c12,[C][N][C][=N][C][N][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=N][=Ring1][#Branch2],\"InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3\"\nCamphor,-1.96,CC1(C)C2CCC1(C)C(=O)C2,[C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2],\"InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3\"\nCaproaldehyde,-1.3,CCCCCC=O,[C][C][C][C][C][C][=O],\"InChI=1S/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3\"\nCarbanilide,-3.15,O=C(Nc1ccccc1)Nc2ccccc2,[O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C13H12N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)\"\nCarbaryl,-3.224,CNC(=O)Oc1cccc2ccccc12,[C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"InChI=1S/C12H11NO2/c1-13-12(14)15-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3,(H,13,14)\"\nCarbazole,-5.27,c1ccc2c(c1)[nH]c3ccccc32,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2],\"InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H\"\nCarbetamide,-1.83,c1c(NC(=O)OC(C)C(=O)NCC)cccc1,[C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][O][C][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Ring1][P],\"InChI=1S/C12H16N2O3/c1-3-13-11(15)9(2)17-12(16)14-10-7-5-4-6-8-10/h4-9H,3H2,1-2H3,(H,13,15)(H,14,16)\"\nCarbofuran,-2.8,CNC(=O)Oc1cccc2CC(C)(C)Oc12,[C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][Ring1][O][=Ring1][#Branch1],\"InChI=1S/C12H15NO3/c1-12(2)7-8-5-4-6-9(10(8)16-12)15-11(14)13-3/h4-6H,7H2,1-3H3,(H,13,14)\"\nCarbophenthion,-5.736,CCOP(=S)(OCC)SCSc1ccc(Cl)cc1,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C11H16ClO2PS3/c1-3-13-15(16,14-4-2)18-9-17-11-7-5-10(12)6-8-11/h5-8H,3-4,9H2,1-2H3\"\nCarboxin,-3.14,CC1=C(SCCO1)C(=O)Nc2ccccc2,[C][C][=C][Branch1][#Branch1][S][C][C][O][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\"\nCarbromal,-2.68,CCC(Br)(CC)C(=O)NC(N)=O,[C][C][C][Branch1][C][Br][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][Branch1][C][N][=O],\"InChI=1S/C7H13BrN2O2/c1-3-7(8,4-2)5(11)10-6(9)12/h3-4H2,1-2H3,(H3,9,10,11,12)\"\nCarvacrol,-2.08,c1(O)c(C)ccc(C(C)C)c1,[C][Branch1][C][O][=C][Branch1][C][C][C][=C][C][Branch1][=Branch1][C][Branch1][C][C][C][=C][Ring1][O],\"InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3\"\nCarvone,-2.06,CC(=C)C1CC=C(C)C(=O)C1,[C][C][=Branch1][C][=C][C][C][C][=C][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2],\"InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3\"\nChloramphenicol,-2.111,OCC(NC(=O)C(Cl)Cl)C(O)c1ccc(cc1)N(=O)=O,[O][C][C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl][C][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)\"\nChlorazine,-4.411,CCN(CC)c1nc(Cl)nc(n1)N(CC)CC,[C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C],\"InChI=1S/C11H20ClN5/c1-5-16(6-2)10-13-9(12)14-11(15-10)17(7-3)8-4/h5-8H2,1-4H3\"\nChlorbromuron,-3.924,CON(C)C(=O)Nc1ccc(Br)c(Cl)c1,[C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C9H10BrClN2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\"\nChlorbufam,-2.617,CC(OC(=O)Nc1cccc(Cl)c1)C#C,[C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][#C],\"InChI=1S/C11H10ClNO2/c1-3-8(2)15-11(14)13-10-6-4-5-9(12)7-10/h1,4-8H,2H3,(H,13,14)\"\nChlordane,-6.86,ClC1CC2C(C1Cl)C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl,[Cl][C][C][C][C][Branch1][Branch1][C][Ring1][Branch1][Cl][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl],\"InChI=1S/C10H6Cl8/c11-3-1-2-4(5(3)12)9(16)7(14)6(13)8(2,15)10(9,17)18/h2-5H,1H2\"\nchlordimeform,-2.86,CN(C)C=Nc1ccc(Cl)cc1C,[C][N][Branch1][C][C][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C],\"InChI=1S/C10H13ClN2/c1-8-6-9(11)4-5-10(8)12-7-13(2)3/h4-7H,1-3H3\"\nChlorimuron-ethyl (ph 7),-4.576,CCOC(=O)c1ccccc1S(=O)(=O)NN(C=O)c2nc(Cl)cc(OC)n2,[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][N][Branch1][Ring1][C][=O][C][=N][C][Branch1][C][Cl][=C][C][Branch1][Ring1][O][C][=N][Ring1][=Branch2],\"InChI=1S/C15H15ClN4O6S/c1-3-26-14(22)10-6-4-5-7-11(10)27(23,24)19-20(9-21)15-17-12(16)8-13(18-15)25-2/h4-9,19H,3H2,1-2H3\"\nChloroacetonitrile,-0.092,ClCC#N,[Cl][C][C][#N],InChI=1S/C2H2ClN/c3-1-2-4/h1H2\nChlorobenzene,-2.38,Clc1ccccc1,[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C6H5Cl/c7-6-4-2-1-3-5-6/h1-5H\nChlorodibromethane,-1.9,ClC(Br)Br,[Cl][C][Branch1][C][Br][Br],InChI=1S/CHBr2Cl/c2-1(3)4/h1H\nChloroethane,-1.06,ClCC,[Cl][C][C],\"InChI=1S/C2H5Cl/c1-2-3/h2H2,1H3\"\nChloroethylene,-1.75,ClC=C,[Cl][C][=C],\"InChI=1S/C2H3Cl/c1-2-3/h2H,1H2\"\nChloropham,-3.38,CC(C)OC(=O)Nc1cccc(Cl)c1,[C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],\"InChI=1S/C10H12ClNO2/c1-7(2)14-10(13)12-9-5-3-4-8(11)6-9/h3-7H,1-2H3,(H,12,13)\"\nChloropicrin,-2,ClC(Cl)(Cl)N(=O)=O,[Cl][C][Branch1][C][Cl][Branch1][C][Cl][N][=Branch1][C][=O][=O],\"InChI=1S/CCl3NO2/c2-1(3,4)5(6)7\"\nchloropropylate,-4.53,c1ccc(Cl)cc1C(c2ccc(Cl)cc2)(O)C(=O)OC(C)C,[C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][O][C][Branch1][C][C][C],\"InChI=1S/C17H16Cl2O3/c1-11(2)22-16(20)17(21,12-6-8-14(18)9-7-12)13-4-3-5-15(19)10-13/h3-11,21H,1-2H3\"\nChlorothalonil,-5.64,c1(C#N)c(Cl)c(C#N)c(Cl)c(Cl)c(Cl)1,[C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][Ring1][=N],InChI=1S/C8Cl4N2/c9-5-3(1-13)6(10)8(12)7(11)4(5)2-14\nChlorotoluron,-3.46,CN(C)C(=O)Nc1ccc(C)c(Cl)c1,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\"\nChloroxuron,-4.89,CN(C)C(=O)Nc2ccc(Oc1ccc(Cl)cc1)cc2,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Ring1][=C],\"InChI=1S/C15H15ClN2O2/c1-18(2)15(19)17-12-5-9-14(10-6-12)20-13-7-3-11(16)4-8-13/h3-10H,1-2H3,(H,17,19)\"\nChlorthalidone,-3.451,NS(=O)(=O)c1cc(ccc1Cl)C2(O)NC(=O)c3ccccc23,[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1],\"InChI=1S/C14H11ClN2O4S/c15-11-6-5-8(7-12(11)22(16,20)21)14(19)10-4-2-1-3-9(10)13(18)17-14/h1-7,19H,(H,17,18)(H2,16,20,21)\"\nChlortoluron,-3.483,CN(C)C(=O)Nc1ccc(C)c(Cl)c1,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\"\nChlorzoxazone,-2.831,Clc2ccc1oc(=O)[nH]c1c2,[Cl][C][=C][C][=C][O][C][=Branch1][C][=O][NH1][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"InChI=1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)\"\nCholanthrene,-7.85,C1Cc2c3c1cccc3cc4c2ccc5ccccc54,[C][C][C][=C][C][Ring1][Branch1][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2],\"InChI=1S/C20H14/c1-2-7-16-13(4-1)8-10-17-18-11-9-14-5-3-6-15(20(14)18)12-19(16)17/h1-8,10,12H,9,11H2\"\nChrysene,-8.057,c1ccc2c(c1)ccc3c4ccccc4ccc23,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#C][Ring1][#Branch2],InChI=1S/C18H12/c1-3-7-15-13(5-1)9-11-18-16-8-4-2-6-14(16)10-12-17(15)18/h1-12H\n\"cis 1,2-Dichloroethylene\",-1.3,Cl\\C=C/Cl,[Cl][\\C][=C][/Cl],InChI=1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-\n\"cis-1,2-Dimethylcyclohexane\",-4.3,C/C1CCCCC1\\C,[C][/C][C][C][C][C][C][Ring1][=Branch1][\\C],\"InChI=1S/C8H16/c1-7-5-3-4-6-8(7)2/h7-8H,3-6H2,1-2H3\"\ncis-2-Pentene,-2.54,CC/C=C\\C,[C][C][/C][=C][\\C],\"InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3-\"\ncitral,-2.06,CC(C)=CCCC(C)=CC(=O),[C][C][Branch1][C][C][=C][C][C][C][Branch1][C][C][=C][C][=O],\"InChI=1S/C10H16O/c1-9(2)5-4-6-10(3)7-8-11/h5,7-8H,4,6H2,1-3H3\"\nClomazone,-2.338,CC1(C)CON(Cc2ccccc2Cl)C1=O,[C][C][Branch1][C][C][C][O][N][Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][Ring1][=C][=O],\"InChI=1S/C12H14ClNO2/c1-12(2)8-16-14(11(12)15)7-9-5-3-4-6-10(9)13/h3-6H,7-8H2,1-2H3\"\nClonazepam,-3.499,Clc1ccccc1C2=NCC(=O)Nc3ccc(cc23)N(=O)=O,[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][N][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C15H10ClN3O3/c16-12-4-2-1-3-10(12)15-11-7-9(19(21)22)5-6-13(11)18-14(20)8-17-15/h1-7H,8H2,(H,18,20)\"\nCoronene,-9.332,c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67,[C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][C][C][Ring1][S][=C][Ring1][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H\nCorticosterone,-3.24,CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO,[C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][C][=Branch1][C][=O][C][O],\"InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3\"\nCortisone,-3.11,CC12CC(=O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO,[C][C][C][C][=Branch1][C][=O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O],\"InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-15,18,22,26H,3-8,10-11H2,1-2H3\"\nCoumachlor,-5.839,CC(=O)CC(c1ccc(Cl)cc1)c2c(O)c3ccccc3oc2=O,[C][C][=Branch1][C][=O][C][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][O][=O],\"InChI=1S/C19H15ClO4/c1-11(21)10-15(12-6-8-13(20)9-7-12)17-18(22)14-4-2-3-5-16(14)24-19(17)23/h2-9,15,22H,10H2,1H3\"\nCoumaphos,-5.382,CCOP(=S)(OCC)Oc2ccc1oc(=O)c(Cl)c(C)c1c2,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][O][C][=Branch1][C][=O][C][Branch1][C][Cl][=C][Branch1][C][C][C][Ring1][=Branch2][=C][Ring1][=N],\"InChI=1S/C14H16ClO5PS/c1-4-17-21(22,18-5-2)20-10-6-7-12-11(8-10)9(3)13(15)14(16)19-12/h6-8H,4-5H2,1-3H3\"\nCyanazine,-3.15,CCNc1nc(Cl)nc(NC(C)(C)C#N)n1,[C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][O][N][C][Branch1][C][C][Branch1][C][C][C][#N][=N][Ring1][=N],\"InChI=1S/C9H13ClN6/c1-4-12-7-13-6(10)14-8(15-7)16-9(2,3)5-11/h4H2,1-3H3,(H2,12,13,14,15,16)\"\nCyclobutyl-5-spirobarbituric acid,-1.655,O=C2NC(=O)C1(CCC1)C(=O)N2,[O][=C][N][C][=Branch1][C][=O][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=Branch1][C][=O][N][Ring1][O],\"InChI=1S/C7H8N2O3/c10-4-7(2-1-3-7)5(11)9-6(12)8-4/h1-3H2,(H2,8,9,10,11,12)\"\nCycloheptane,-3.51,C1CCCCCC1,[C][C][C][C][C][C][C][Ring1][#Branch1],InChI=1S/C7H14/c1-2-4-6-7-5-3-1/h1-7H2\nCycloheptanol,-0.88,OC1CCCCCC1,[O][C][C][C][C][C][C][C][Ring1][#Branch1],\"InChI=1S/C7H14O/c8-7-5-3-1-2-4-6-7/h7-8H,1-6H2\"\nCycloheptene,-3.18,C1CCC=CCC1,[C][C][C][C][=C][C][C][Ring1][#Branch1],\"InChI=1S/C7H12/c1-2-4-6-7-5-3-1/h1-2H,3-7H2\"\nCyclohexane,-3.1,C1CCCCC1,[C][C][C][C][C][C][Ring1][=Branch1],InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2\nCyclohexanol ,-0.44,OC1CCCCC1,[O][C][C][C][C][C][C][Ring1][=Branch1],\"InChI=1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2\"\nCyclohexanone,-0.6,O=C1CCCCC1,[O][=C][C][C][C][C][C][Ring1][=Branch1],InChI=1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2\nCyclohexene,-2.59,C1CCC=CC1,[C][C][C][C][=C][C][Ring1][=Branch1],\"InChI=1S/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2\"\nCyclohexyl-5-spirobarbituric acid,-3.06,O=C2NC(=O)C1(CCCCC1)C(=O)N2,[O][=C][N][C][=Branch1][C][=O][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][=N],\"InChI=1S/C9H12N2O3/c12-6-9(4-2-1-3-5-9)7(13)11-8(14)10-6/h1-5H2,(H2,10,11,12,13,14)\"\nCyclooctane,-4.15,C1CCCCCCC1,[C][C][C][C][C][C][C][C][Ring1][Branch2],InChI=1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2\nCyclooctanol,-1.29,OC1CCCCCCC1,[O][C][C][C][C][C][C][C][C][Ring1][Branch2],\"InChI=1S/C8H16O/c9-8-6-4-2-1-3-5-7-8/h8-9H,1-7H2\"\nCyclooctyl-5-spirobarbituric acid,-2.982,O=C2NC(=O)C1(CCCCCCC1)C(=O)N2,[O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch2][C][C][C][C][C][C][C][Ring1][Branch2][C][=Branch1][C][=O][N][Ring1][#C],\"InChI=1S/C11H16N2O3/c14-8-11(9(15)13-10(16)12-8)6-4-2-1-3-5-7-11/h1-7H2,(H2,12,13,14,15,16)\"\nCyclopentane ,-2.64,C1CCCC1,[C][C][C][C][C][Ring1][Branch1],InChI=1S/C5H10/c1-2-4-5-3-1/h1-5H2\nCyclopentene ,-2.1,C1CC=CC1,[C][C][C][=C][C][Ring1][Branch1],\"InChI=1S/C5H8/c1-2-4-5-3-1/h1-2H,3-5H2\"\nCyclopentyl-5-spirobarbituric acid,-2.349,O=C2NC(=O)C1(CCCC1)C(=O)N2,[O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][N],\"InChI=1S/C8H10N2O3/c11-5-8(3-1-2-4-8)6(12)10-7(13)9-5/h1-4H2,(H2,9,10,11,12,13)\"\nCycluron,-2.218,CN(C)C(=O)NC1CCCCCCC1,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][C][Ring1][Branch2],\"InChI=1S/C11H22N2O/c1-13(2)11(14)12-10-8-6-4-3-5-7-9-10/h10H,3-9H2,1-2H3,(H,12,14)\"\nCyfluthrin,-7.337,CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2ccc(F)c(Oc3ccccc3)c2,[C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][Branch1][C][F][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C],\"InChI=1S/C22H18Cl2FNO3/c1-22(2)15(11-19(23)24)20(22)21(27)29-18(12-26)13-8-9-16(25)17(10-13)28-14-6-4-3-5-7-14/h3-11,15,18,20H,1-2H3\"\nCyhalothrin,-8.176,CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2,[C][C][Branch1][C][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][O][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N],\"InChI=1S/C23H19ClF3NO3/c1-22(2)17(12-19(24)23(25,26)27)20(22)21(29)31-18(13-28)14-7-6-10-16(11-14)30-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\"\nCypermethrin,-8.017,CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2,[C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N],\"InChI=1S/C22H19Cl2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\"\nDanazol,-5.507,CC23Cc1cnoc1C=C2CCC4C3CCC5(C)C4CCC5(O)C#C,[C][C][C][C][C][=N][O][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][C][C][C][C][Ring1][=N][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][Branch1][C][O][C][#C],\"InChI=1S/C22H27NO2/c1-4-22(24)10-8-18-16-6-5-15-11-19-14(13-23-25-19)12-20(15,2)17(16)7-9-21(18,22)3/h1,11,13,16-18,24H,5-10,12H2,2-3H3\"\nDapsone,-3.094,Nc1ccc(cc1)S(=O)(=O)c2ccc(N)cc2,[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2\"\nDDD,-7.2,ClC(Cl)C(c1ccc(Cl)cc1)c2ccc(Cl)cc2,[Cl][C][Branch1][C][Cl][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C14H10Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8,13-14H\"\nDDE,-6.9,ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2,[Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\nDDT,-7.15,Clc1ccc(cc1)C(c2ccc(Cl)cc2)C(Cl)(Cl)Cl,[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C14H9Cl5/c15-11-5-1-9(2-6-11)13(14(17,18)19)10-3-7-12(16)8-4-10/h1-8,13H\"\nDecalin,-5.19,C1CCC2CCCCC2C1,[C][C][C][C][C][C][C][C][C][Ring1][=Branch1][C][Ring1][#Branch2],\"InChI=1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2\"\nDEF,-5.14,CCCCSP(=O)(SCCCC)SCCCC,[C][C][C][C][S][P][=Branch1][C][=O][Branch1][=Branch1][S][C][C][C][C][S][C][C][C][C],\"InChI=1S/C12H27OPS3/c1-4-7-10-15-14(13,16-11-8-5-2)17-12-9-6-3/h4-12H2,1-3H3\"\nDeltamethrin,-8.402,CC1(C)C(C=C(Br)Br)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2,[C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Br][Br][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N],\"InChI=1S/C22H19Br2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\"\nDeoxycorticosterone,-3.45,CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO,[C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][O],\"InChI=1S/C21H30O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h11,15-18,22H,3-10,12H2,1-2H3\"\nDexamethasone,-3.59,CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO,[C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][C][Branch1][C][C][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O],\"InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3\"\nD-fenchone,-1.85,CC2(C)C1CCC(C)(C1)C2=O,[C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][=O],\"InChI=1S/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3\"\nDi(2-ethylhexyl)-phthalate,-6.96,CCCCC(CC)COC(=O)c1ccccc1C(=O)OCC(CC)CCCC,[C][C][C][C][C][Branch1][Ring1][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][Branch1][Ring1][C][C][C][C][C][C],\"InChI=1S/C24H38O4/c1-5-9-13-19(7-3)17-27-23(25)21-15-11-12-16-22(21)24(26)28-18-20(8-4)14-10-6-2/h11-12,15-16,19-20H,5-10,13-14,17-18H2,1-4H3\"\nDialifor,-6.34,CCOP(=S)(OCC)SC(CCl)N1C(=O)c2ccccc2C1=O,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O],\"InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\"\nDialifos,-6.34,CCOP(=S)(OCC)SC(CCl)N2C(=O)c1ccccc1C2=O,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O],\"InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\"\nDiallate,-4.286,CC(C)N(C(C)C)C(=O)SCC(=CCl)Cl,[C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][=Branch1][Ring1][=C][Cl][Cl],\"InChI=1S/C10H17Cl2NOS/c1-7(2)13(8(3)4)10(14)15-6-9(12)5-11/h5,7-8H,6H2,1-4H3\"\nDiazepam,-3.754,CN2C(=O)CN=C(c1ccccc1)c3cc(Cl)ccc23,[C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#Branch1],\"InChI=1S/C16H13ClN2O/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\"\nDiazinon,-3.64,CCOP(=S)(OCC)Oc1cc(C)nc(n1)C(C)C,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][Branch1][C][C][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][Branch1][C][C][C],\"InChI=1S/C12H21N2O3PS/c1-6-15-18(19,16-7-2)17-11-8-10(5)13-12(14-11)9(3)4/h8-9H,6-7H2,1-5H3\"\nDibenzofurane,-4.6,o1c2ccccc2c3ccccc13,[O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],InChI=1S/C12H8O/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\nDibenzothiophene,-4.38,c1ccc2c(c1)sc3ccccc23,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\nDibromomethane,-1.17,BrCBr,[Br][C][Br],InChI=1S/CH2Br2/c2-1-3/h1H2\nDibutyl ether ,-1.85,CCCCOCCCC,[C][C][C][C][O][C][C][C][C],\"InChI=1S/C8H18O/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3\"\ndibutyl sebacate,-3.896,CCCCOC(=O)CCCCCCCCC(=O)OCCCC,[C][C][C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C][C][C],\"InChI=1S/C18H34O4/c1-3-5-15-21-17(19)13-11-9-7-8-10-12-14-18(20)22-16-6-4-2/h3-16H2,1-2H3\"\nDicapthon,-4.31,COP(=S)(OC)Oc1ccc(cc1Cl)N(=O)=O,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O],\"InChI=1S/C8H9ClNO5PS/c1-13-16(17,14-2)15-8-4-3-6(10(11)12)5-7(8)9/h3-5H,1-2H3\"\nDichloromethane,-0.63,ClCCl,[Cl][C][Cl],InChI=1S/CH2Cl2/c2-1-3/h1H2\nDichlorophen,-3.953,Oc1ccc(Cl)cc1Cc2cc(Cl)ccc2O,[O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O],\"InChI=1S/C13H10Cl2O2/c14-10-1-3-12(16)8(6-10)5-9-7-11(15)2-4-13(9)17/h1-4,6-7,16-17H,5H2\"\nDicofol,-5.666,OC(c1ccc(Cl)cc1)(c2ccc(Cl)cc2)C(Cl)(Cl)Cl,[O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C14H9Cl5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H\"\nDieldrin,-6.29,ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl,[Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl],\"InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\"\nDienestrol,-4.95,CC=C(C(=CC)c1ccc(O)cc1)c2ccc(O)cc2,[C][C][=C][Branch1][P][C][=Branch1][Ring1][=C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C18H18O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h3-12,19-20H,1-2H3\"\nDienochlor,-7.278,ClC1=C(Cl)C(Cl)(C(=C1Cl)Cl)C2(Cl)C(=C(Cl)C(=C2Cl)Cl)Cl,[Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][=Branch2][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][C][Branch1][C][Cl][C][=Branch1][=N][=C][Branch1][C][Cl][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][Cl],\"InChI=1S/C10Cl10/c11-1-2(12)6(16)9(19,5(1)15)10(20)7(17)3(13)4(14)8(10)18\"\nDiethyl ether ,-0.09,CCOCC,[C][C][O][C][C],\"InChI=1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3\"\nDiethyl phthalate ,-2.35,CCOC(=O)c1ccccc1C(=O)OCC,[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C12H14O4/c1-3-15-11(13)9-7-5-6-8-10(9)12(14)16-4-2/h5-8H,3-4H2,1-2H3\"\nDiethyl sulfide,-1.34,CCSCC,[C][C][S][C][C],\"InChI=1S/C4H10S/c1-3-5-4-2/h3-4H2,1-2H3\"\nDiethyldisulfide,-2.42,CCSSCC,[C][C][S][S][C][C],\"InChI=1S/C4H10S2/c1-3-5-6-4-2/h3-4H2,1-2H3\"\nDifenoxuron,-4.16,COc2ccc(Oc1ccc(NC(=O)N(C)C)cc1)cc2,[C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][C][=C][Ring2][Ring1][Ring1],\"InChI=1S/C16H18N2O3/c1-18(2)16(19)17-12-4-6-14(7-5-12)21-15-10-8-13(20-3)9-11-15/h4-11H,1-3H3,(H,17,19)\"\ndifluron,-6.02,Fc1cccc(F)c1C(=O)NC(=O)Nc2ccc(Cl)cc2,[F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C14H9ClF2N2O2/c15-8-4-6-9(7-5-8)18-14(21)19-13(20)12-10(16)2-1-3-11(12)17/h1-7H,(H2,18,19,20,21)\"\nDihexyl phthalate,-6.144,CCCCCCOC(=O)c1ccccc1C(=O)OCCCCCC,[C][C][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][C][C][C][C],\"InChI=1S/C20H30O4/c1-3-5-7-11-15-23-19(21)17-13-9-10-14-18(17)20(22)24-16-12-8-6-4-2/h9-10,13-14H,3-8,11-12,15-16H2,1-2H3\"\nDiiodomethane,-2.34,ICI,[I][C][I],InChI=1S/CH2I2/c2-1-3/h1H2\ndiisooctyl phthalate,-6.637,c1(C(=O)OCCCCCC(C)(C))c(C(=O)OCCCCCC(C)(C))cccc1,[C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][=C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][=C][Ring2][Ring1][N],\"InChI=1S/C24H38O4/c1-19(2)13-7-5-11-17-27-23(25)21-15-9-10-16-22(21)24(26)28-18-12-6-8-14-20(3)4/h9-10,15-16,19-20H,5-8,11-14,17-18H2,1-4H3\"\nDiisopropyl ether ,-1.1,CC(C)OC(C)C,[C][C][Branch1][C][C][O][C][Branch1][C][C][C],\"InChI=1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3\"\nDiisopropylsulfide,-2.24,CC(C)SC(C)C,[C][C][Branch1][C][C][S][C][Branch1][C][C][C],\"InChI=1S/C6H14S/c1-5(2)7-6(3)4/h5-6H,1-4H3\"\nDimecron,0.523,CCN(CC)C(=O)C(=CCOP(=O)(OC)OC)Cl,[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Cl],\"InChI=1S/C10H19ClNO5P/c1-5-12(6-2)10(13)9(11)7-8-17-18(14,15-3)16-4/h7H,5-6,8H2,1-4H3\"\nDimefuron,-4.328,CN(C)C(=O)Nc1ccc(c(Cl)c1)n2nc(oc2=O)C(C)(C)C,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C15H19ClN4O3/c1-15(2,3)12-18-20(14(22)23-12)11-7-6-9(8-10(11)16)17-13(21)19(4)5/h6-8H,1-5H3,(H,17,21)\"\nDimethoxymethane,0.48,COCOC,[C][O][C][O][C],\"InChI=1S/C3H8O2/c1-4-3-5-2/h3H2,1-2H3\"\nDimethyl phthalate,-1.66,COC(=O)c1ccccc1C(=O)OC,[C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C],\"InChI=1S/C10H10O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-6H,1-2H3\"\nDimethyl sulfide,-0.45,CSC,[C][S][C],InChI=1S/C2H6S/c1-3-2/h1-2H3\nDimethyldisulfide,-1.44,CSSC,[C][S][S][C],InChI=1S/C2H6S2/c1-3-4-2/h1-2H3\nDinitramine,-5.47,CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O,[C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O],\"InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\"\nd-inositol,0.35,OC1C(O)C(O)C(O)C(O)C1O,[O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O],InChI=1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H\nDi-n-propylsulfide,-2.58,CCCSCCC,[C][C][C][S][C][C][C],\"InChI=1S/C6H14S/c1-3-5-7-6-4-2/h3-6H2,1-2H3\"\nDiosgenin,-7.32,C1C(O)CCC2(C)CC3CCC4(C)C5(C)CC6OCC(C)CC6OC5CC4C3C=C21,[C][C][Branch1][C][O][C][C][C][Branch1][C][C][C][C][C][C][C][Branch1][C][C][C][Branch1][C][C][C][C][O][C][C][Branch1][C][C][C][C][Ring1][#Branch1][O][C][Ring1][N][C][C][Ring1][S][C][Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=C],\"InChI=1S/C27H42O3/c1-16-9-22-23(29-15-16)14-27(4)24(30-22)12-21-20-11-18-10-19(28)6-7-25(18,2)13-17(20)5-8-26(21,27)3/h11,16-17,19-24,28H,5-10,12-15H2,1-4H3\"\nDioxacarb,-1.57,CNC(=O)Oc1ccccc1C2OCCO2,[C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][C][O][Ring1][Branch1],\"InChI=1S/C11H13NO4/c1-12-11(13)16-9-5-3-2-4-8(9)10-14-6-7-15-10/h2-5,10H,6-7H2,1H3,(H,12,13)\"\nDiphenyl ether ,-3.96,O(c1ccccc1)c2ccccc2,[O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H\nDiphenylamine,-3.504,N(c1ccccc1)c2ccccc2,[N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H\"\nDiphenylmethane,-4.08,C(c1ccccc1)c2ccccc2,[C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2\"\nDipropyl ether,-1.62,CCCOCCC,[C][C][C][O][C][C][C],\"InChI=1S/C6H14O/c1-3-5-7-6-4-2/h3-6H2,1-2H3\"\nDisulfiram,-4.86,CCN(CC)C(=S)SSC(=S)N(CC)CC,[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][S][C][=Branch1][C][=S][N][Branch1][Ring1][C][C][C][C],\"InChI=1S/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H3\"\nDisulfoton,-4.23,CCOP(=S)(OCC)SCCSCC,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][C][S][C][C],\"InChI=1S/C8H19O2PS3/c1-4-9-11(12,10-5-2)14-8-7-13-6-3/h4-8H2,1-3H3\"\nDitalimfos,-3.35,CCOP(=S)(OCC)N2C(=O)c1ccccc1C2=O,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O],\"InChI=1S/C12H14NO4PS/c1-3-16-18(19,17-4-2)13-11(14)9-7-5-6-8-10(9)12(13)15/h5-8H,3-4H2,1-2H3\"\nDiuron,-3.8,CN(C)C(=O)Nc1ccc(Cl)c(Cl)c1,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C9H10Cl2N2O/c1-13(2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\"\nd-Limonene,-4.26,CC1=CCC(CC1)C(C)=C,[C][C][=C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][=C],\"InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3\"\nDNOC,-1.456,Cc1cc(cc(N(=O)=O)c1O)N(=O)=O,[C][C][=C][C][=Branch1][=C][=C][C][Branch1][=Branch1][N][=Branch1][C][=O][=O][=C][Ring1][=Branch2][O][N][=Branch1][C][=O][=O],\"InChI=1S/C7H6N2O5/c1-4-2-5(8(11)12)3-6(7(4)10)9(13)14/h2-3,10H,1H3\"\nDulcin,-2.17,CCOc1ccc(NC(N)=O)cc1,[C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][Branch1][C][N][=O][C][=C][Ring1][#Branch2],\"InChI=1S/C9H12N2O2/c1-2-13-8-5-3-7(4-6-8)11-9(10)12/h3-6H,2H2,1H3,(H3,10,11,12)\"\nDyphylline,-0.17,Cn2c(=O)n(C)c1ncn(CC(O)CO)c1c2=O,[C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][Branch2][C][C][Branch1][C][O][C][O][C][=Ring1][#Branch2][C][Ring1][S][=O],\"InChI=1S/C10H14N4O4/c1-12-8-7(9(17)13(2)10(12)18)14(5-11-8)3-6(16)4-15/h5-6,15-16H,3-4H2,1-2H3\"\nEicosane,-8.172,CCCCCCCCCCCCCCCCCCCC,[C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C],\"InChI=1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3\"\nEndrin,-6.18,ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl,[Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl],\"InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\"\nEpiandrosterone,-4.16,CC34CCC1C(CCC2CC(O)CCC12C)C3CCC4=O,[C][C][C][C][C][C][Branch1][P][C][C][C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O],\"InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\"\nEpitostanol,-5.41,CC45CCC2C(CCC3CC1SC1CC23C)C4CCC5O,[C][C][C][C][C][C][Branch1][P][C][C][C][C][C][S][C][Ring1][Ring1][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O],\"InChI=1S/C19H30OS/c1-18-8-7-14-12(13(18)5-6-17(18)20)4-3-11-9-15-16(21-15)10-19(11,14)2/h11-17,20H,3-10H2,1-2H3\"\nEquilenin,-5.24,CC34CCc1c(ccc2cc(O)ccc12)C3CCC4=O,[C][C][C][C][C][=C][Branch1][S][C][=C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O],\"InChI=1S/C18H18O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h2-5,10,16,19H,6-9H2,1H3\"\nEquilin,-5.282,CC34CCC1C(=CCc2cc(O)ccc12)C3CCC4=O,[C][C][C][C][C][C][=Branch1][S][=C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O],\"InChI=1S/C18H20O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3-5,10,14,16,19H,2,6-9H2,1H3\"\nEriodictyol,-3.62,Oc2cc(O)c1C(=O)CC(Oc1c2)c3ccc(O)c(O)c3,[O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2],\"InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2\"\nErythritol,0.7,OCC(O)C(O)CO,[O][C][C][Branch1][C][O][C][Branch1][C][O][C][O],\"InChI=1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2\"\nEstradiol,-5.03,CC12CCC3C(CCc4cc(O)ccc34)C2CCC1O,[C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][O],\"InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3\"\nEstragole,-2.92,c1(OC)ccc(CC=C)cc1,[C][Branch1][Ring1][O][C][=C][C][=C][Branch1][Ring2][C][C][=C][C][=C][Ring1][O],\"InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3,5-8H,1,4H2,2H3\"\nEstrone,-3.955,CC12CCC3C(CCc4cc(O)ccc34)C2CCC1=O,[C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O],\"InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3\"\nEthalfluralin,-6.124,CCN(CC(C)=C)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O,[C][C][N][Branch1][#Branch1][C][C][Branch1][C][C][=C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O],\"InChI=1S/C13H14F3N3O4/c1-4-17(7-8(2)3)12-10(18(20)21)5-9(13(14,15)16)6-11(12)19(22)23/h5-6H,2,4,7H2,1,3H3\"\nEthane,-1.36,CC,[C][C],InChI=1S/C2H6/c1-2/h1-2H3\nEthanethiol,-0.6,CCS,[C][C][S],\"InChI=1S/C2H6S/c1-2-3/h3H,2H2,1H3\"\nEthanol,1.1,CCO,[C][C][O],\"InChI=1S/C2H6O/c1-2-3/h3H,2H2,1H3\"\nEthion,-5.54,CCOP(=S)(OCC)SCSP(=S)(OCC)OCC,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C],\"InChI=1S/C9H22O4P2S4/c1-5-10-14(16,11-6-2)18-9-19-15(17,12-7-3)13-8-4/h5-9H2,1-4H3\"\nEthirimol,-3.028,CCCCc1c(C)nc(NCC)[nH]c1=O,[C][C][C][C][C][=C][Branch1][C][C][N][=C][Branch1][Ring2][N][C][C][NH1][C][Ring1][#Branch2][=O],\"InChI=1S/C11H19N3O/c1-4-6-7-9-8(3)13-11(12-5-2)14-10(9)15/h4-7H2,1-3H3,(H2,12,13,14,15)\"\nEthofumesate,-3.42,CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C,[C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C],\"InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\"\nethofumesate,-3.42,CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C,[C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C],\"InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\"\nEthyl acetate,-0.04,CCOC(=O)C,[C][C][O][C][=Branch1][C][=O][C],\"InChI=1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3\"\nEthyl benzoate ,-2.32,CCOC(=O)c1ccccc1,[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C9H10O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3\"\nEthyl butyrate,-1.28,CCCCCOC(=O)CC,[C][C][C][C][C][O][C][=Branch1][C][=O][C][C],\"InChI=1S/C8H16O2/c1-3-5-6-7-10-8(9)4-2/h3-7H2,1-2H3\"\nethyl cinnamate,-3,CCOC(=O)C=Cc1ccccc1,[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3\"\nEthyl decanoate,-4.1,CCCCCCCCCC(=O)OCC,[C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C12H24O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h3-11H2,1-2H3\"\nEthyl formate,0.15,CCOC=O,[C][C][O][C][=O],\"InChI=1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3\"\nEthyl heptanoate,-2.74,CCCCCCC(=O)OCC,[C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C9H18O2/c1-3-5-6-7-8-9(10)11-4-2/h3-8H2,1-2H3\"\nEthyl hexanoate,-2.35,CCCCCC(=O)OCC,[C][C][C][C][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C8H16O2/c1-3-5-6-7-8(9)10-4-2/h3-7H2,1-2H3\"\nEthyl nonanoate,-3.8,CCCCCCCCC(=O)OCC,[C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C11H22O2/c1-3-5-6-7-8-9-10-11(12)13-4-2/h3-10H2,1-2H3\"\nEthyl octanoate,-3.39,CCCCCCCC(=O)OCC,[C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C10H20O2/c1-3-5-6-7-8-9-10(11)12-4-2/h3-9H2,1-2H3\"\nEthyl pentanoate,-1.75,CCCOC(=O)CCC,[C][C][C][O][C][=Branch1][C][=O][C][C][C],\"InChI=1S/C7H14O2/c1-3-5-7(8)9-6-4-2/h3-6H2,1-2H3\"\nEthyl propionate,-0.66,CCOC(=O)CC,[C][C][O][C][=Branch1][C][=O][C][C],\"InChI=1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3\"\nEthyl propyl ether,-0.66,CCCOCC,[C][C][C][O][C][C],\"InChI=1S/C5H12O/c1-3-5-6-4-2/h3-5H2,1-2H3\"\nEthyl vinyl ether,-0.85,CCOC=C,[C][C][O][C][=C],\"InChI=1S/C4H8O/c1-3-5-4-2/h3H,1,4H2,2H3\"\nEthylbenzene,-2.77,CCc1ccccc1,[C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3\"\nEthylcyclohexane,-4.25,CCC1CCCCC1,[C][C][C][C][C][C][C][C][Ring1][=Branch1],\"InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3\"\nEthylene,-0.4,C=C,[C][=C],InChI=1S/C2H4/c1-2/h1-2H2\nEthyl-p-aminobenzoate,-2.1,CCOC(=O)c1ccc(N)cc1,[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\"\nEthyl-p-hydroxybenzoate ,-2.35,CCOC(=O)c1ccc(O)cc1,[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C9H10O3/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3\"\nEthyne,0.29,C#C,[C][#C],InChI=1S/C2H2/c1-2/h1-2H\nEtofenprox,-8.6,CCOc1ccc(cc1)C(C)(C)COCc3cccc(Oc2ccccc2)c3,[C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N],\"InChI=1S/C25H28O3/c1-4-27-22-15-13-21(14-16-22)25(2,3)19-26-18-20-9-8-12-24(17-20)28-23-10-6-5-7-11-23/h5-17H,4,18-19H2,1-3H3\"\nEtomidate,-4.735,CCOC(=O)c1cncn1C(C)c2ccccc2,[C][C][O][C][=Branch1][C][=O][C][=C][N][=C][N][Ring1][Branch1][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C14H16N2O2/c1-3-18-14(17)13-9-15-10-16(13)11(2)12-7-5-4-6-8-12/h4-11H,3H2,1-2H3\"\n\"Etoposide (148-167,25mg/ml)\",-3.571,COc1cc(cc(OC)c1O)C6C2C(COC2=O)C(OC4OC3COC(C)OC3C(O)C4O)c7cc5OCOc5cc67,[C][O][C][=C][C][=Branch1][O][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][C][Branch1][#Branch1][C][O][C][Ring1][Branch1][=O][C][Branch2][Ring1][#Branch1][O][C][O][C][C][O][C][Branch1][C][C][O][C][Ring1][#Branch1][C][Branch1][C][O][C][Ring1][N][O][C][=C][C][O][C][O][C][=Ring1][Branch1][C][=C][Ring2][Ring1][#C][Ring1][=Branch2],\"InChI=1S/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3\"\nEugenol,-1.56,COc1cc(CC=C)ccc1O,[C][O][C][=C][C][Branch1][Ring2][C][C][=C][=C][C][=C][Ring1][=Branch2][O],\"InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3,5-7,11H,1,4H2,2H3\"\nFenarimol,-4.38,OC(c1ccc(Cl)cc1)(c2cncnc2)c3ccccc3Cl,[O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][=Branch2][C][=C][N][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],\"InChI=1S/C17H12Cl2N2O/c18-14-7-5-12(6-8-14)17(22,13-9-20-11-21-10-13)15-3-1-2-4-16(15)19/h1-11,22H\"\nFenfuram,-3.3,Cc1occc1C(=O)Nc2ccccc2,[C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H11NO2/c1-9-11(7-8-15-9)12(14)13-10-5-3-2-4-6-10/h2-8H,1H3,(H,13,14)\"\nFenitrothion,-4.04,COP(=S)(OC)Oc1ccc(N(=O)=O)c(C)c1,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][=C][Ring1][#Branch2],\"InChI=1S/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3\"\nFenothiocarb,-3.927,CN(C)C(=O)SCCCCOc1ccccc1,[C][N][Branch1][C][C][C][=Branch1][C][=O][S][C][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C13H19NO2S/c1-14(2)13(15)17-11-7-6-10-16-12-8-4-3-5-9-12/h3-5,8-9H,6-7,10-11H2,1-2H3\"\nFenoxycarb,-4.7,CCOC(=O)NCCOc2ccc(Oc1ccccc1)cc2,[C][C][O][C][=Branch1][C][=O][N][C][C][O][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N],\"InChI=1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19)\"\nFenpropathrin,-6.025,CC1(C)C(C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2)C1(C)C,[C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][Ring2][Ring1][#Branch1][Branch1][C][C][C],\"InChI=1S/C22H23NO3/c1-21(2)19(22(21,3)4)20(24)26-18(14-23)15-9-8-12-17(13-15)25-16-10-6-5-7-11-16/h5-13,18-19H,1-4H3\"\nFenthion,-4.57,COP(=S)(OC)Oc1ccc(SC)c(C)c1,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][Ring1][S][C][C][Branch1][C][C][=C][Ring1][=Branch2],\"InChI=1S/C10H15O3PS2/c1-8-7-9(5-6-10(8)16-4)13-14(15,11-2)12-3/h5-7H,1-4H3\"\nFenuron,-1.6,CN(C)C(=O)Nc1ccccc1,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C9H12N2O/c1-11(2)9(12)10-8-6-4-3-5-7-8/h3-7H,1-2H3,(H,10,12)\"\nFlucythrinate,-6.876,CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1)c3ccc(OC(F)F)cc3,[C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][C][=C][Branch1][#Branch1][O][C][Branch1][C][F][F][C][=C][Ring1][#Branch2],\"InChI=1S/C26H23F2NO4/c1-17(2)24(18-11-13-21(14-12-18)32-26(27)28)25(30)33-23(16-29)19-7-6-10-22(15-19)31-20-8-4-3-5-9-20/h3-15,17,23-24,26H,1-2H3\"\nFlucytosine,-0.972,Nc1nc(=O)[nH]cc1F,[N][C][=N][C][=Branch1][C][=O][NH1][C][=C][Ring1][#Branch1][F],\"InChI=1S/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9)\"\nFlumethasone,-5.613,CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO,[C][C][C][C][C][C][C][Branch1][C][F][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][Ring1][Branch1][C][C][C][Ring2][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O],\"InChI=1S/C22H28F2O5/c1-11-6-13-14-8-16(23)15-7-12(26)4-5-19(15,2)21(14,24)17(27)9-20(13,3)22(11,29)18(28)10-25/h4-5,7,11,13-14,16-17,25,27,29H,6,8-10H2,1-3H3\"\nFlumetralin,-6.78,CCN(Cc1c(F)cccc1Cl)c2c(cc(cc2N(=O)=O)C(F)(F)F)N(=O)=O,[C][C][N][Branch1][=C][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][Cl][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O],\"InChI=1S/C16H12ClF4N3O4/c1-2-22(8-10-11(17)4-3-5-12(10)18)15-13(23(25)26)6-9(16(19,20)21)7-14(15)24(27)28/h3-7H,2,8H2,1H3\"\nFluometuron,-3.43,CN(C)C(=O)Nc1cccc(c1)C(F)(F)F,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\"\nFluoranthene,-6,c1ccc2c(c1)c3cccc4cccc2c34,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1],InChI=1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H\nFluorene ,-5,C1c2ccccc2c3ccccc13,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"InChI=1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2\"\nFluorobenzene,-1.8,Fc1ccccc1,[F][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H\nFluoromethalone,-4.099,CC1CC2C3CCC(O)(C(=O)C)C3(C)CC(O)C2(F)C4(C)C=CC(=O)C=C14,[C][C][C][C][C][C][C][C][Branch1][C][O][Branch1][=Branch1][C][=Branch1][C][=O][C][C][Ring1][=Branch2][Branch1][C][C][C][C][Branch1][C][O][C][Ring1][#C][Branch1][C][F][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2],\"InChI=1S/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3\"\nFluorometuron,-3.32,CN(C)C(=O)Nc1cccc(c1)C(F)(F)F,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\"\nFluridone,-4.445,Cn2cc(c1ccccc1)c(=O)c(c2)c3cccc(c3)C(F)(F)F,[C][N][C][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][Ring2][=C][Ring1][=N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"InChI=1S/C19H14F3NO/c1-23-11-16(13-6-3-2-4-7-13)18(24)17(12-23)14-8-5-9-15(10-14)19(20,21)22/h2-12H,1H3\"\nFlurochloridone,-4.047,FC(F)(F)c1cccc(c1)N2CC(CCl)C(Cl)C2=O,[F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][Branch1][Ring1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][=O],\"InChI=1S/C12H10Cl2F3NO/c13-5-7-6-18(11(19)10(7)14)9-3-1-2-8(4-9)12(15,16)17/h1-4,7,10H,5-6H2\"\nFlutriafol,-3.37,OC(Cn1cncn1)(c2ccc(F)cc2)c3ccccc3F,[O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][F],\"InChI=1S/C16H13F2N3O/c17-13-7-5-12(6-8-13)16(22,9-21-11-19-10-20-21)14-3-1-2-4-15(14)18/h1-8,10-11,22H,9H2\"\nFluvalinate,-8.003,CC(C)C(Nc1ccc(cc1Cl)C(F)(F)F)C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2,[C][C][Branch1][C][C][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N],\"InChI=1S/C26H22ClF3N2O3/c1-16(2)24(32-22-12-11-18(14-21(22)27)26(28,29)30)25(33)35-23(15-31)17-7-6-10-20(13-17)34-19-8-4-3-5-9-19/h3-14,16,23-24,32H,1-2H3\"\nFormetanate,-2.34,CNC(=O)Oc1cccc(N=CN(C)C)c1,[C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][Branch1][Branch2][N][=C][N][Branch1][C][C][C][=C][Ring1][O],\"InChI=1S/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)\"\nFormothion,-1.995,COP(=S)(OC)SCC(=O)N(C)C=O,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=O],\"InChI=1S/C6H12NO4PS2/c1-7(5-8)6(9)4-14-12(13,10-2)11-3/h5H,4H2,1-3H3\"\nFructose,0.64,OCC1OC(O)(CO)C(O)C1O,[O][C][C][O][C][Branch1][C][O][Branch1][Ring1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O],\"InChI=1S/C6H12O6/c7-1-3-4(9)5(10)6(11,2-8)12-3/h3-5,7-11H,1-2H2\"\nFurane,-0.82,c1ccoc1,[C][C][=C][O][C][=Ring1][Branch1],InChI=1S/C4H4O/c1-2-4-5-3-1/h1-4H\nFurfural,-0.1,O=Cc1ccco1,[O][=C][C][=C][C][=C][O][Ring1][Branch1],InChI=1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H\ngentisin,-2.943,c1c(O)C2C(=O)C3cc(O)ccC3OC2cc1(OC),[C][=C][Branch1][C][O][C][C][=Branch1][C][=O][C][C][=C][Branch1][C][O][C][=C][C][Ring1][#Branch1][O][C][Ring1][N][C][=C][Ring1][P][O][C],\"InChI=1S/C14H14O5/c1-18-8-5-10(16)13-12(6-8)19-11-3-2-7(15)4-9(11)14(13)17/h2-6,9,11-13,15-16H,1H3\"\nGlafenine,-4.571,OCC(O)COC(=O)c1ccccc1Nc2ccnc3cc(Cl)ccc23,[O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1],\"InChI=1S/C19H17ClN2O4/c20-12-5-6-14-17(7-8-21-18(14)9-12)22-16-4-2-1-3-15(16)19(25)26-11-13(24)10-23/h1-9,13,23-24H,10-11H2,(H,21,22)\"\nglucose,0.74,OCC1OC(O)C(O)C(O)C1O,[O][C][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O],\"InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2\"\nGlycerol,1.12,OCC(O)CO,[O][C][C][Branch1][C][O][C][O],\"InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2\"\nGlyceryl triacetate,-0.6,CC(=O)OCC(COC(=O)C)OC(=O)C,[C][C][=Branch1][C][=O][O][C][C][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][O][C][=Branch1][C][=O][C],\"InChI=1S/C9H14O6/c1-6(10)13-4-9(15-8(3)12)5-14-7(2)11/h9H,4-5H2,1-3H3\"\nGriseofulvin,-3.246,COC1=CC(=O)CC(C)C13Oc2c(Cl)c(OC)cc(OC)c2C3=O,[C][O][C][=C][C][=Branch1][C][=O][C][C][Branch1][C][C][C][Ring1][Branch2][O][C][=C][Branch1][C][Cl][C][Branch1][Ring1][O][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][O][C][Ring1][=C][=O],\"InChI=1S/C17H17ClO6/c1-8-5-9(19)6-12(23-4)17(8)16(20)13-10(21-2)7-11(22-3)14(18)15(13)24-17/h6-8H,5H2,1-4H3\"\nhematein,-2.7,c1cc(O)c(O)c2OCC3(O)CC4=CC(=O)C(O)=CC4=C3c21,[C][=C][C][Branch1][C][O][=C][Branch1][C][O][C][O][C][C][Branch1][C][O][C][C][=C][C][=Branch1][C][=O][C][Branch1][C][O][=C][C][Ring1][Branch2][=C][Ring1][N][C][=Ring1][S][Ring2][Ring1][=Branch1],\"InChI=1S/C16H12O6/c17-10-2-1-8-13-9-4-12(19)11(18)3-7(9)5-16(13,21)6-22-15(8)14(10)20/h1-4,17,19-21H,5-6H2\"\nHeptachlor,-6.317,ClC1C=CC2C1C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl,[Cl][C][C][=C][C][C][Ring1][Branch1][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl],\"InChI=1S/C10H5Cl7/c11-4-2-1-3-5(4)9(15)7(13)6(12)8(3,14)10(9,16)17/h1-5H\"\nHeptane,-4.53,CCCCCCC,[C][C][C][C][C][C][C],\"InChI=1S/C7H16/c1-3-5-7-6-4-2/h3-7H2,1-2H3\"\n\"Hexachloro-1,3-butadiene\",-4.92,ClC(=C(Cl)C(=C(Cl)Cl)Cl)Cl,[Cl][C][=Branch1][=C][=C][Branch1][C][Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl][Cl],InChI=1S/C4Cl6/c5-1(3(7)8)2(6)4(9)10\nHexachloroethane,-3.67,ClC(Cl)(Cl)C(Cl)(Cl)Cl,[Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C2Cl6/c3-1(4,5)2(6,7)8\"\nhexacosane,-8.334,CCCCCCCCCCCCCCCCCCCCCCCCCC,[C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C],\"InChI=1S/C26H54/c1-3-5-7-9-11-13-15-17-19-21-23-25-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-26H2,1-2H3\"\nHexadecane,-8.4,CCCCCCCCCCCCCCCC,[C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C],\"InChI=1S/C16H34/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3-16H2,1-2H3\"\nHexamethylbenzene,-5.23,Cc1c(C)c(C)c(C)c(C)c1C,[C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][#Branch2][C],InChI=1S/C12H18/c1-7-8(2)10(4)12(6)11(5)9(7)3/h1-6H3\nHexane ,-3.84,CCCCCC,[C][C][C][C][C][C],\"InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3\"\nHexestrol,-4.43,CCC(C(CC)c1ccc(O)cc1)c2ccc(O)cc2,[C][C][C][Branch1][P][C][Branch1][Ring1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C18H22O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,17-20H,3-4H2,1-2H3\"\nHexylbenzene ,-5.21,CCCCCCc1ccccc1,[C][C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H18/c1-2-3-4-6-9-12-10-7-5-8-11-12/h5,7-8,10-11H,2-4,6,9H2,1H3\"\nhydrobenzoin,-1.93,c1ccccc1C(O)C(O)c2ccccc2,[C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H\"\nHydrocortisone ,-3.09,CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO,[C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O],\"InChI=1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3\"\nHydrocortisone 21-acetate,-4.88,CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3C(O)CC21C,[C][C][=Branch1][C][=O][O][C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][Branch1][C][O][C][C][Ring1][P][Ring2][Ring1][Branch1][C],\"InChI=1S/C23H32O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h10,16-18,20,26,28H,4-9,11-12H2,1-3H3\"\nHydroxyprogesterone-17a,-3.817,CC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C,[C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C],\"InChI=1S/C21H30O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h12,16-18,24H,4-11H2,1-3H3\"\nIndan,-3.04,C1Cc2ccccc2C1,[C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2],\"InChI=1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2\"\nIndole,-1.52,c2ccc1[nH]ccc1c2,[C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2],\"InChI=1S/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9H\"\nInosine,-1.23,OCC1OC(C(O)C1O)n2cnc3c(O)ncnc23,[O][C][C][O][C][Branch1][=Branch2][C][Branch1][C][O][C][Ring1][=Branch1][O][N][C][=N][C][=C][Branch1][C][O][N][=C][N][=C][Ring1][#Branch2][Ring1][#Branch1],\"InChI=1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)\"\nIodobenzene,-3.01,Ic1ccccc1,[I][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C6H5I/c7-6-4-2-1-3-5-6/h1-5H\nIodoethane,-1.6,CCI,[C][C][I],\"InChI=1S/C2H5I/c1-2-3/h2H2,1H3\"\nIodofenphos,-6.62,COP(=S)(OC)Oc1cc(Cl)c(I)cc1Cl,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][I][C][=C][Ring1][Branch2][Cl],\"InChI=1S/C8H8Cl2IO3PS/c1-12-15(16,13-2)14-8-4-5(9)7(11)3-6(8)10/h3-4H,1-2H3\"\nIodomethane,-1,CI,[C][I],InChI=1S/CH3I/c1-2/h1H3\nIoxynil,-3.61,Oc1c(I)cc(C#N)cc1I,[O][C][=C][Branch1][C][I][C][=C][Branch1][Ring1][C][#N][C][=C][Ring1][=Branch2][I],\"InChI=1S/C7H3I2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H\"\nIpazine,-3.785,CCN(CC)c1nc(Cl)nc(NC(C)C)n1,[C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O],\"InChI=1S/C10H18ClN5/c1-5-16(6-2)10-14-8(11)13-9(15-10)12-7(3)4/h7H,5-6H2,1-4H3,(H,12,13,14,15)\"\nIsazofos,-3.658,CCOP(=S)(OCC)Oc1nc(Cl)n(n1)C(C)C,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][N][=C][Branch1][C][Cl][N][Branch1][Ring2][N][=Ring1][=Branch1][C][Branch1][C][C][C],\"InChI=1S/C9H17ClN3O3PS/c1-5-14-17(18,15-6-2)16-9-11-8(10)13(12-9)7(3)4/h7H,5-6H2,1-4H3\"\nIsobutyl acetate,-1.21,CC(C)COC(=O)C,[C][C][Branch1][C][C][C][O][C][=Branch1][C][=O][C],\"InChI=1S/C6H12O2/c1-5(2)4-8-6(3)7/h5H,4H2,1-3H3\"\nIsobutyl formate,-1.01,CC(C)COC=O,[C][C][Branch1][C][C][C][O][C][=O],\"InChI=1S/C5H10O2/c1-5(2)3-7-4-6/h4-5H,3H2,1-2H3\"\nIsobutylbenzene,-4.12,CC(C)Cc1ccccc1,[C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C10H14/c1-9(2)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3\"\nisocarbamid,-2.15,C1N(C(=O)NCC(C)C)C(=O)NC1,[C][N][Branch1][N][C][=Branch1][C][=O][N][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][Ring1][=N],\"InChI=1S/C8H15N3O2/c1-6(2)5-10-8(13)11-4-3-9-7(11)12/h6H,3-5H2,1-2H3,(H,9,12)(H,10,13)\"\nIsocarboxazid,-2.461,Cc1cc(no1)C(=O)NNCc2ccccc2,[C][C][=C][C][=Branch1][Branch1][=N][O][Ring1][Branch1][C][=Branch1][C][=O][N][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H13N3O2/c1-9-7-11(15-17-9)12(16)14-13-8-10-5-3-2-4-6-10/h2-7,13H,8H2,1H3,(H,14,16)\"\nIsofenphos,-4.194,CCOP(=S)(NC(C)C)Oc1ccccc1C(=O)OC(C)C,[C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][N][C][Branch1][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][C][C],\"InChI=1S/C15H24NO4PS/c1-6-18-21(22,16-11(2)3)20-14-10-8-7-9-13(14)15(17)19-12(4)5/h7-12H,6H2,1-5H3,(H,16,22)\"\nIsonazid,0.009,c1nccc(C(=O)NN)c1,[C][=N][C][=C][C][Branch1][#Branch1][C][=Branch1][C][=O][N][N][=C][Ring1][#Branch2],\"InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)\"\nIsopentyl acetate,-1.92,CC(C)CCOC(=O)C,[C][C][Branch1][C][C][C][C][O][C][=Branch1][C][=O][C],\"InChI=1S/C7H14O2/c1-6(2)4-5-9-7(3)8/h6H,4-5H2,1-3H3\"\nIsopentyl formate,-1.52,CC(C)CCOC=O,[C][C][Branch1][C][C][C][C][O][C][=O],\"InChI=1S/C6H12O2/c1-6(2)3-4-8-5-7/h5-6H,3-4H2,1-2H3\"\nIsoprocarb,-2.863,CNC(=O)Oc1ccccc1C(C)C,[C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][C][C],\"InChI=1S/C11H15NO2/c1-8(2)9-6-4-5-7-10(9)14-11(13)12-3/h4-8H,1-3H3,(H,12,13)\"\nIsopropalin,-6.49,CCCN(CCC)c1c(cc(cc1N(=O)=O)C(C)C)N(=O)=O,[C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][C][N][=Branch1][C][=O][=O],\"InChI=1S/C15H23N3O4/c1-5-7-16(8-6-2)15-13(17(19)20)9-12(11(3)4)10-14(15)18(21)22/h9-11H,5-8H2,1-4H3\"\nIsopropyl acetate,-0.55,CC(C)OC(=O)C,[C][C][Branch1][C][C][O][C][=Branch1][C][=O][C],\"InChI=1S/C5H10O2/c1-4(2)7-5(3)6/h4H,1-3H3\"\nIsopropyl formate,-0.63,CC(C)OC=O,[C][C][Branch1][C][C][O][C][=O],\"InChI=1S/C4H8O2/c1-4(2)6-3-5/h3-4H,1-2H3\"\nIsopropylbenzene ,-3.27,CC(C)c1ccccc1,[C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C9H12/c1-8(2)9-6-4-3-5-7-9/h3-8H,1-2H3\"\nIsoproturon,-3.536,CC(C)c1ccc(NC(=O)N(C)C)cc1,[C][C][Branch1][C][C][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N],\"InChI=1S/C12H18N2O/c1-9(2)10-5-7-11(8-6-10)13-12(15)14(3)4/h5-9H,1-4H3,(H,13,15)\"\nIsoquinoline,-1.45,c1ccc2cnccc2c1,[C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H\nkebuzone,-3.27,CC(=O)CCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3,[C][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C19H18N2O3/c1-14(22)12-13-17-18(23)20(15-8-4-2-5-9-15)21(19(17)24)16-10-6-3-7-11-16/h2-11,17H,12-13H2,1H3\"\nKepone,-5.259,ClC1(C(=O)C2(Cl)C3(Cl)C14Cl)C5(Cl)C2(Cl)C3(Cl)C(Cl)(Cl)C45Cl,[Cl][C][Branch1][P][C][=Branch1][C][=O][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][Cl][C][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring1][N][Ring1][#Branch2][Cl],\"InChI=1S/C10Cl10O/c11-2-1(21)3(12)6(15)4(2,13)8(17)5(2,14)7(3,16)9(6,18)10(8,19)20\"\nLactose,-0.244,OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O,[O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O],\"InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\"\nL-arabinose,0.39,C1OC(O)C(O)C(O)C1O,[C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O],\"InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2\"\nLenacil,-4.594,O=c2[nH]c1CCCc1c(=O)n2C3CCCCC3,[O][=C][NH1][C][C][C][C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][#Branch2][C][C][C][C][C][C][Ring1][=Branch1],\"InChI=1S/C13H18N2O2/c16-12-10-7-4-8-11(10)14-13(17)15(12)9-5-2-1-3-6-9/h9H,1-8H2,(H,14,17)\"\nlinalool,-1.99,CC(C)=CCCC(O)(C)C=C,[C][C][Branch1][C][C][=C][C][C][C][Branch1][C][O][Branch1][C][C][C][=C],\"InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3\"\nLindane,-4.64,ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl,[Cl][C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Cl],InChI=1S/C6H6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6H\nLinuron,-3.592,CON(C)C(=O)Nc1ccc(Cl)c(Cl)c1,[C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C9H10Cl2N2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\"\nLorazepam,-3.604,OC3N=C(c1ccccc1Cl)c2cc(Cl)ccc2NC3=O,[O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][C][Ring2][Ring1][Ring1][=O],\"InChI=1S/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)\"\nMalathion,-3.37,CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC,[C][C][O][C][=Branch1][C][=O][C][C][Branch1][N][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C10H19O6PS2/c1-5-15-9(11)7-8(10(12)16-6-2)19-17(18,13-3)14-4/h8H,5-7H2,1-4H3\"\nMalonic acid diethylester,-0.82,CCOC(=O)CC(=O)OCC,[C][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C7H12O4/c1-3-10-6(8)5-7(9)11-4-2/h3-5H2,1-2H3\"\nMaltose,0.358,OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O,[O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O],\"InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\"\nm-Chloroaniline,-1.37,Nc1cccc(Cl)c1,[N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],\"InChI=1S/C6H6ClN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2\"\nm-Chlorobromobenzene,-3.21,Clc1cccc(Br)c1,[Cl][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1],InChI=1S/C6H4BrCl/c7-5-2-1-3-6(8)4-5/h1-4H\nm-Chloroiodobenzene,-3.55,Clc1cccc(I)c1,[Cl][C][=C][C][=C][C][Branch1][C][I][=C][Ring1][#Branch1],InChI=1S/C6H4ClI/c7-5-2-1-3-6(8)4-5/h1-4H\nm-Chloronitrobenzene ,-2.77,Clc1cccc(c1)N(=O)=O,[Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],InChI=1S/C6H4ClNO2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H\nMebendazole,-3.88,COC(=O)Nc2nc1ccc(cc1[nH]2)C(=O)c3ccccc3,[C][O][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)\"\nMecarbam,-2.518,CCOC(=O)N(C)C(=O)CSP(=S)(OCC)OCC,[C][C][O][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C],\"InChI=1S/C10H20NO5PS2/c1-5-14-10(13)11(4)9(12)8-19-17(18,15-6-2)16-7-3/h5-8H2,1-4H3\"\nmeconin,-1.899,c1c(OC)c(OC)C2C(=O)OCC2c1,[C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][C][=Branch1][C][=O][O][C][C][Ring1][=Branch1][C][=Ring1][=C],\"InChI=1S/C10H12O4/c1-12-7-4-3-6-5-14-10(11)8(6)9(7)13-2/h3-4,6,8H,5H2,1-2H3\"\nMedrogestone,-5.27,CC(=O)C3(C)CCC4C2C=C(C)C1=CC(=O)CCC1(C)C2CCC34C,[C][C][=Branch1][C][=O][C][Branch1][C][C][C][C][C][C][C][=C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][C][C][C][Ring2][Ring1][Branch1][Ring1][P][C],\"InChI=1S/C23H32O2/c1-14-12-17-18(21(3)9-6-16(25)13-20(14)21)7-11-23(5)19(17)8-10-22(23,4)15(2)24/h12-13,17-19H,6-11H2,1-5H3\"\nMefenacet,-4.873,CN(C(=O)COc1nc2ccccc2s1)c3ccccc3,[C][N][Branch2][Ring1][Ring2][C][=Branch1][C][=O][C][O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C16H14N2O2S/c1-18(12-7-3-2-4-8-12)15(19)11-20-16-17-13-9-5-6-10-14(13)21-16/h2-10H,11H2,1H3\"\nMefluidide,-3.24,CC(=O)Nc1cc(NS(=O)(=O)C(F)(F)F)c(C)cc1C,[C][C][=Branch1][C][=O][N][C][=C][C][Branch1][P][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][=C][Branch1][C][C][C][=C][Ring1][#C][C],\"InChI=1S/C11H13F3N2O3S/c1-6-4-7(2)10(5-9(6)15-8(3)17)16-20(18,19)11(12,13)14/h4-5,16H,1-3H3,(H,15,17)\"\nMenthone,-2.35,CC(C)C1CCC(C)CC1=O,[C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][Ring1][#Branch1][=O],\"InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3\"\nMethane,-0.9,C,[C],InChI=1S/CH4/h1H4\nMethanol,1.57,CO,[C][O],\"InChI=1S/CH4O/c1-2/h2H,1H3\"\nMethaqualone,-2.925,Cc1ccccc1n3c(C)nc2ccccc2c3=O,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=O],\"InChI=1S/C16H14N2O/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19/h3-10H,1-2H3\"\nMethazole,-2.82,Cn2c(=O)on(c1ccc(Cl)c(Cl)c1)c2=O,[C][N][C][=Branch1][C][=O][O][N][Branch1][#C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring1][=C][=O],\"InChI=1S/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3\"\nMethocarbamol,-0.985,COc1ccccc1OCC(O)COC(N)=O,[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O][C][Branch1][C][N][=O],\"InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)\"\nMethoprene,-5.19,COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C,[C][O][C][Branch1][C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][Branch1][C][C][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C],\"InChI=1S/C19H34O3/c1-15(2)22-18(20)14-17(4)11-8-10-16(3)12-9-13-19(5,6)21-7/h8,11,14-16H,9-10,12-13H2,1-7H3\"\nMethoproptryne,-2.928,COCCCNc1nc(NC(C)C)nc(SC)n1,[C][O][C][C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N],\"InChI=1S/C11H21N5OS/c1-8(2)13-10-14-9(12-6-5-7-17-3)15-11(16-10)18-4/h8H,5-7H2,1-4H3,(H2,12,13,14,15,16)\"\nMethoxychlor,-6.89,COc1ccc(cc1)C(c2ccc(OC)cc2)C(Cl)(Cl)Cl,[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C16H15Cl3O2/c1-20-13-7-3-11(4-8-13)15(16(17,18)19)12-5-9-14(21-2)10-6-12/h3-10,15H,1-2H3\"\nMethyl acetate,0.46,COC(=O)C,[C][O][C][=Branch1][C][=O][C],InChI=1S/C3H6O2/c1-3(4)5-2/h1-2H3\nMethyl acrylate,-0.22,COC(=O)C=C,[C][O][C][=Branch1][C][=O][C][=C],\"InChI=1S/C4H6O2/c1-3-4(5)6-2/h3H,1H2,2H3\"\nMethyl benzoate ,-1.85,COC(=O)c1ccccc1,[C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H8O2/c1-10-8(9)7-5-3-2-4-6-7/h2-6H,1H3\"\nMethyl butyl ether ,-0.99,CCCCOC,[C][C][C][C][O][C],\"InChI=1S/C5H12O/c1-3-4-5-6-2/h3-5H2,1-2H3\"\nMethyl butyrate,-0.82,CCCOC(=O)CC,[C][C][C][O][C][=Branch1][C][=O][C][C],\"InChI=1S/C6H12O2/c1-3-5-8-6(7)4-2/h3-5H2,1-2H3\"\nMethyl decanoate,-4.69,CCCCCCCCCC(=O)OC,[C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C11H22O2/c1-3-4-5-6-7-8-9-10-11(12)13-2/h3-10H2,1-2H3\"\nMethyl formate,0.58,COC=O,[C][O][C][=O],\"InChI=1S/C2H4O2/c1-4-2-3/h2H,1H3\"\nMethyl hexanoate,-1.87,CCCCCC(=O)OC,[C][C][C][C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C7H14O2/c1-3-4-5-6-7(8)9-2/h3-6H2,1-2H3\"\nMethyl hydrazine,1.34,CNN,[C][N][N],\"InChI=1S/CH6N2/c1-3-2/h3H,2H2,1H3\"\nmethyl laurate,-4.69,CCCCCCCCCCCC(=O)OC,[C][C][C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3\"\nMethyl nonanoate,-3.38,CCCCCCCCC(=O)OC,[C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C10H20O2/c1-3-4-5-6-7-8-9-10(11)12-2/h3-9H2,1-2H3\"\nMethyl octanoate,-3.17,CCCCCCCC(=O)OC,[C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C9H18O2/c1-3-4-5-6-7-8-9(10)11-2/h3-8H2,1-2H3\"\nMethyl pentanoate,-1.36,CCCC(=O)OCC,[C][C][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C6H12O2/c1-3-5-6(7)8-4-2/h3-5H2,1-2H3\"\nMethyl propionate,-0.14,CCC(=O)OC,[C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C4H8O2/c1-3-4(5)6-2/h3H2,1-2H3\"\nMethyl propyl ether ,-0.39,CCCOC,[C][C][C][O][C],\"InChI=1S/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3\"\nMethyl t-butyl ether ,-0.24,COC(C)(C)C,[C][O][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C5H12O/c1-5(2,3)6-4/h1-4H3\"\nMethylcyclohexane ,-3.85,CC1CCCCC1,[C][C][C][C][C][C][C][Ring1][=Branch1],\"InChI=1S/C7H14/c1-7-5-3-2-4-6-7/h7H,2-6H2,1H3\"\nMethylcyclopentane,-3.3,CC1CCCC1,[C][C][C][C][C][C][Ring1][Branch1],\"InChI=1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3\"\nMethyldymron,-3.35,CN(C(=O)NC(C)(C)c1ccccc1)c2ccccc2,[C][N][Branch2][Ring1][Branch1][C][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C17H20N2O/c1-17(2,14-10-6-4-7-11-14)18-16(20)19(3)15-12-8-5-9-13-15/h4-13H,1-3H3,(H,18,20)\"\nMethylparaben,-1.827,COC(=O)c1ccc(O)cc1,[C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C8H8O3/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5,9H,1H3\"\nmethylthiouracil,-2.436,Cc1cc(=O)[nH]c(=S)[nH]1,[C][C][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=S][NH1][Ring1][Branch2],\"InChI=1S/C5H6N2OS/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)\"\nMetolcarb,-1.803,c1ccccc1(OC(=O)NC),[C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][N][C],\"InChI=1S/C8H9NO2/c1-9-8(10)11-7-5-3-2-4-6-7/h2-6H,1H3,(H,9,10)\"\nMetoxuron,-2.564,COc1ccc(NC(=O)N(C)C)cc1Cl,[C][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][Cl],\"InChI=1S/C10H13ClN2O2/c1-13(2)10(14)12-7-4-5-9(15-3)8(11)6-7/h4-6H,1-3H3,(H,12,14)\"\nMetribuzin,-2.253,CSc1nnc(c(=O)n1N)C(C)(C)C,[C][S][C][=N][N][=C][Branch1][=Branch2][C][=Branch1][C][=O][N][Ring1][#Branch1][N][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C8H14N4OS/c1-8(2,3)5-6(13)12(9)7(14-4)11-10-5/h9H2,1-4H3\"\nMetronidazole,-1.22,Cc1ncc(N(=O)=O)n1CCO,[C][C][=N][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][N][Ring1][Branch2][C][C][O],\"InChI=1S/C6H9N3O3/c1-5-7-4-6(9(11)12)8(5)2-3-10/h4,10H,2-3H2,1H3\"\nm-Fluorobromobenzene,-2.67,Fc1cccc(Br)c1,[F][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1],InChI=1S/C6H4BrF/c7-5-2-1-3-6(8)4-5/h1-4H\nMirex,-6.8,ClC1(C2(Cl)C3(Cl)C4(Cl)C5(Cl)C1(Cl)C3(Cl)Cl)C5(Cl)C(Cl)(Cl)C24Cl,[Cl][C][Branch2][Ring1][=C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring2][Ring1][Ring1][Ring1][#C][Cl],\"InChI=1S/C10Cl12/c11-1-2(12)7(17)4(14)3(13,5(1,15)9(7,19)20)6(1,16)10(21,22)8(2,4)18\"\nm-Methylaniline,-0.85,Cc1cccc(N)c1,[C][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1],\"InChI=1S/C7H9N/c1-6-3-2-4-7(8)5-6/h2-5H,8H2,1H3\"\nm-Nitroaniline,-2.19,Nc1cccc(c1)N(=O)=O,[N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C6H6N2O2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H,7H2\"\nm-Nitrophenol,-1.01,Oc1cccc(c1)N(=O)=O,[O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C6H5NO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H\"\nm-Nitrotoluene,-2.44,Cc1cccc(c1)N(=O)=O,[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C7H7NO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3\"\nMonolinuron,-2.57,CON(C)C(=O)Nc1ccc(Cl)cc1,[C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C9H11ClN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\"\nMonotropitoside,-0.742,COC(=O)c1ccccc1OC2OC(COC3OCC(O)C(O)C3O)C(O)C(O)C2O,[C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][O][C][Branch2][Ring1][C][C][O][C][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring1][O],\"InChI=1S/C19H26O12/c1-27-17(26)8-4-2-3-5-10(8)30-19-16(25)14(23)13(22)11(31-19)7-29-18-15(24)12(21)9(20)6-28-18/h2-5,9,11-16,18-25H,6-7H2,1H3\"\nMonuron,-2.89,CN(C)C(=O)Nc1ccc(Cl)cc1,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\"\nm-Xylene ,-2.82,Cc1cccc(C)c1,[C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1],\"InChI=1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3\"\n\"N,N-Diethylaniline\",-3.03,CCN(CC)c1ccccc1,[C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3\"\n\"N,N-Dimethylacetamide\",1.11,CN(C)C(=O)C,[C][N][Branch1][C][C][C][=Branch1][C][=O][C],InChI=1S/C4H9NO/c1-4(6)5(2)3/h1-3H3\n\"N,N-Dimethylaniline\",-1.92,CN(C)c1ccccc1,[C][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3\"\nNaled,-2.28,COP(=O)(OC)OC(Br)C(Cl)(Cl)Br,[C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Branch1][C][Br][C][Branch1][C][Cl][Branch1][C][Cl][Br],\"InChI=1S/C4H7Br2Cl2O4P/c1-10-13(9,11-2)12-3(5)4(6,7)8/h3H,1-2H3\"\nNapthacene,-8.6,c1ccc2cc3cc4ccccc4cc3cc2c1,[C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][C][Ring1][=C][=C][Ring2][Ring1][C],InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H\nNapthalene,-3.6,c1ccc2ccccc2c1,[C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H\nNeburon,-4.77,CCCCN(C)C(=O)Nc1ccc(Cl)c(Cl)c1,[C][C][C][C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C12H16Cl2N2O/c1-3-4-7-16(2)12(17)15-9-5-6-10(13)11(14)8-9/h5-6,8H,3-4,7H2,1-2H3,(H,15,17)\"\nNerol,-2.46,CC(C)=CCC/C(C)=C\\CO,[C][C][Branch1][C][C][=C][C][C][/C][Branch1][C][C][=C][\\C][O],\"InChI=1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7-\"\nN-Ethylaniline,-1.7,CCNc1ccccc1,[C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H11N/c1-2-9-8-6-4-3-5-7-8/h3-7,9H,2H2,1H3\"\nNiclosamide,-4.7,Oc1ccc(Cl)cc1C(=O)Nc2ccc(cc2Cl)N(=O)=O,[O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O],\"InChI=1S/C13H8Cl2N2O4/c14-7-1-4-12(18)9(5-7)13(19)16-11-3-2-8(17(20)21)6-10(11)15/h1-6,18H,(H,16,19)\"\nNimetazepam,-3.796,CN2C(=O)CN=C(c1ccccc1)c3cc(ccc23)N(=O)=O,[C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C16H13N3O3/c1-18-14-8-7-12(19(21)22)9-13(14)16(17-10-15(18)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\"\nNiridazole,-3.22,O=C1NCCN1c2ncc(s2)N(=O)=O,[O][=C][N][C][C][N][Ring1][Branch1][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C6H6N4O3S/c11-5-7-1-2-9(5)6-8-3-4(14-6)10(12)13/h3H,1-2H2,(H,7,11)\"\nNitramine,-3.561,CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O,[C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O],\"InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\"\nNitrapyrin,-3.76,Clc1cccc(n1)C(Cl)(Cl)Cl,[Cl][C][=C][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C6H3Cl4N/c7-5-3-1-2-4(11-5)6(8,9)10/h1-3H\"\nNitrazepam,-3.796,O=C3CN=C(c1ccccc1)c2cc(ccc2N3)N(=O)=O,[O][=C][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][P][N][=Branch1][C][=O][=O],\"InChI=1S/C15H11N3O3/c19-14-9-16-15(10-4-2-1-3-5-10)12-8-11(18(20)21)6-7-13(12)17-14/h1-8H,9H2,(H,17,19)\"\nNitrobenzene,-1.8,O=N(=O)c1ccccc1,[O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H\nNitroethane,-0.22,CCN(=O)=O,[C][C][N][=Branch1][C][=O][=O],\"InChI=1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3\"\nNitrofen,-5.46,Clc2ccc(Oc1ccc(cc1)N(=O)=O)c(Cl)c2,[Cl][C][=C][C][=C][Branch1][P][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][P],InChI=1S/C12H7Cl2NO3/c13-8-1-6-12(11(14)7-8)18-10-4-2-9(3-5-10)15(16)17/h1-7H\nNitromethane,0.26,CN(=O)=O,[C][N][=Branch1][C][=O][=O],InChI=1S/CH3NO2/c1-2(3)4/h1H3\nN-Methylaniline ,-1.28,CNc1ccccc1,[C][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3\"\nNonane,-5.88,CCCCCCCCC,[C][C][C][C][C][C][C][C][C],\"InChI=1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3\"\nNorea,-3.171,CN(C)C(=O)NC1CC2CC1C3CCCC23,[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][C][C][C][C][Ring1][Branch2][Ring1][Branch1],\"InChI=1S/C13H22N2O/c1-15(2)13(16)14-12-7-8-6-11(12)10-5-3-4-9(8)10/h8-12H,3-7H2,1-2H3,(H,14,16)\"\nnorethindrone acetate,-4.8,CC(=O)OC3(CCC4C2CCC1=CC(=O)CCC1C2CCC34C)C#C,[C][C][=Branch1][C][=O][O][C][Branch2][Ring1][=C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][C][Ring1][O][C][C][C][Ring2][Ring1][C][Ring1][#C][C][C][#C],\"InChI=1S/C22H28O3/c1-4-22(25-14(2)23)12-10-20-19-7-5-15-13-16(24)6-8-17(15)18(19)9-11-21(20,22)3/h1,13,17-20H,5-12H2,2-3H3\"\nNorethisterone,-4.57,CC34CCC1C(CCC2=CC(=O)CCC12O)C3CCC4(O)C#C,[C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][O][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][Branch1][C][O][C][#C],\"InChI=1S/C20H26O3/c1-3-19(22)10-8-16-15-5-4-13-12-14(21)6-11-20(13,23)17(15)7-9-18(16,19)2/h1,12,15-17,22-23H,4-11H2,2H3\"\nnorflurazon,-4.046,CNc2cnn(c1cccc(c1)C(F)(F)F)c(=O)c2Cl,[C][N][C][C][=N][N][Branch2][Ring1][Ring1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][=Ring1][P][Cl],\"InChI=1S/C12H9ClF3N3O/c1-17-9-6-18-19(11(20)10(9)13)8-4-2-3-7(5-8)12(14,15)16/h2-6,17H,1H3\"\no-Aminophenol,-0.72,Nc1ccccc1O,[N][C][=C][C][=C][C][=C][Ring1][=Branch1][O],\"InChI=1S/C6H7NO/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2\"\no-Chloroaniline,-1.52,Nc1ccccc1Cl,[N][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],\"InChI=1S/C6H6ClN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2\"\no-Chlorobromobenzene,-3.19,Clc1ccccc1Br,[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Br],InChI=1S/C6H4BrCl/c7-5-3-1-2-4-6(5)8/h1-4H\no-Chloroiodobenzene,-3.54,Clc1ccccc1I,[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][I],InChI=1S/C6H4ClI/c7-5-3-1-2-4-6(5)8/h1-4H\no-Chloronitrobenzene,-2.55,Clc1ccccc1N(=O)=O,[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],InChI=1S/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H\nOctane,-5.24,CCCCCCCC,[C][C][C][C][C][C][C][C],\"InChI=1S/C8H18/c1-3-5-7-8-6-4-2/h3-8H2,1-2H3\"\nO-Ethyl carbamate,0.85,CCOC(=O)N,[C][C][O][C][=Branch1][C][=O][N],\"InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)\"\no-Fluorobromobenzene,-2.7,Fc1ccccc1Br,[F][C][=C][C][=C][C][=C][Ring1][=Branch1][Br],InChI=1S/C6H4BrF/c7-5-3-1-2-4-6(5)8/h1-4H\no-Hydroxybenzamide,-1.82,NC(=O)c1ccccc1O,[N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O],\"InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\"\no-Methoxyphenol,-1.96,COc1ccccc1O,[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O],\"InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3\"\no-Nitroaniline,-1.96,Nc1ccccc1N(=O)=O,[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C6H6N2O2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H,7H2\"\no-Nitroanisole,-1.96,COc1ccccc1N(=O)=O,[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3\"\no-Nitrophenol,-1.74,Oc1ccccc1N(=O)=O,[O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C6H5NO3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H\"\no-Nitrotoluene,-2.33,Cc1ccccc1N(=O)=O,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C7H7NO2/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3\"\noryzalin,-5.16,CCCN(CCC)c1c(cc(cc1N(=O)=O)S(N)(=O)=O)N(=O)=O,[C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][S][Branch1][C][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O],\"InChI=1S/C12H18N4O6S/c1-3-5-14(6-4-2)12-10(15(17)18)7-9(23(13,21)22)8-11(12)16(19)20/h7-8H,3-6H2,1-2H3,(H2,13,21,22)\"\no-Toluidine,-2.21,Cc1ccccc1N,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][N],\"InChI=1S/C7H9N/c1-6-4-2-3-5-7(6)8/h2-5H,8H2,1H3\"\nOxadiazon,-5.696,CC(C)Oc1cc(c(Cl)cc1Cl)n2nc(oc2=O)C(C)(C)C,[C][C][Branch1][C][C][O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C15H18Cl2N2O3/c1-8(2)21-12-7-11(9(16)6-10(12)17)19-14(20)22-13(18-19)15(3,4)5/h6-8H,1-5H3\"\nOxamyl,0.106,CNC(=O)ON=C(SC)C(=O)N(C)C,[C][N][C][=Branch1][C][=O][O][N][=C][Branch1][Ring1][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C],\"InChI=1S/C7H13N3O3S/c1-8-7(12)13-9-5(14-4)6(11)10(2)3/h1-4H3,(H,8,12)\"\nOxycarboxin,-2.281,CC1=C(C(=O)Nc2ccccc2)S(=O)(=O)CCO1,[C][C][=C][Branch1][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][O][Ring1][P],\"InChI=1S/C12H13NO4S/c1-9-11(18(15,16)8-7-17-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\"\no-Xylene ,-2.8,Cc1ccccc1C,[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C],\"InChI=1S/C8H10/c1-7-5-3-4-6-8(7)2/h3-6H,1-2H3\"\n\"p,p'-Biphenyldiamine \",-2.7,Nc1ccc(cc1)c2ccc(N)cc2,[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\"\n\"P,P'-DDE\",-6.9,ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2,[Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\np-Aminophenol,-0.8,Nc1ccc(O)cc1,[N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C6H7NO/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2\"\nParathion,-4.66,CCOP(=S)(OCC)Oc1ccc(cc1)N(=O)=O,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C10H14NO5PS/c1-3-14-17(18,15-4-2)16-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3\"\np-benzidine,-2.7,Nc1ccc(cc1)c2ccc(N)cc2,[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\"\np-Bromoacetanilide,-3.083,CC(=O)Nc1ccc(Br)cc1,[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],\"InChI=1S/C8H8BrNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\"\np-Bromoiodobenzene,-4.56,Brc1ccc(I)cc1,[Br][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1],InChI=1S/C6H4BrI/c7-5-1-3-6(8)4-2-5/h1-4H\np-Chloroacetanilide,-2.843,CC(=O)Nc1ccc(Cl)cc1,[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C8H8ClNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\"\np-Chloroaniline,-1.66,Nc1ccc(Cl)cc1,[N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"InChI=1S/C6H6ClN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2\"\np-Chlorobromobenzene,-3.63,Clc1ccc(Br)cc1,[Cl][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],InChI=1S/C6H4BrCl/c7-5-1-3-6(8)4-2-5/h1-4H\np-Chloroiodobenzene,-4.03,Clc1ccc(I)cc1,[Cl][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1],InChI=1S/C6H4ClI/c7-5-1-3-6(8)4-2-5/h1-4H\np-Chloronitrobenzene,-2.92,Clc1ccc(cc1)N(=O)=O,[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],InChI=1S/C6H4ClNO2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H\np-Cresol,-0.73,Cc1ccc(O)cc1,[C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C7H8O/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3\"\nPebulate,-3.53,CCCCN(CC)C(=O)SCCC,[C][C][C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][S][C][C][C],\"InChI=1S/C10H21NOS/c1-4-7-8-11(6-3)10(12)13-9-5-2/h4-9H2,1-3H3\"\nPencycuron,-5.915,Clc1ccc(CN(C2CCCC2)C(=O)Nc3ccccc3)cc1,[Cl][C][=C][C][=C][Branch2][Ring1][=Branch2][C][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"InChI=1S/C19H21ClN2O/c20-16-12-10-15(11-13-16)14-22(18-8-4-5-9-18)19(23)21-17-6-2-1-3-7-17/h1-3,6-7,10-13,18H,4-5,8-9,14H2,(H,21,23)\"\nPentachlorobenzene,-5.65,Clc1cc(Cl)c(Cl)c(Cl)c1Cl,[Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl],InChI=1S/C6HCl5/c7-2-1-3(8)5(10)6(11)4(2)9/h1H\nPentachloroethane,-2.6,ClC(Cl)C(Cl)(Cl)Cl,[Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C2HCl5/c3-1(4)2(5,6)7/h1H\"\nPentachlorophenol,-4.28,Oc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl,[O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl],InChI=1S/C6HCl5O/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H\nPentamethylbenzene,-4,Cc1cc(C)c(C)c(C)c1C,[C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][=Branch2][C],\"InChI=1S/C11H16/c1-7-6-8(2)10(4)11(5)9(7)3/h6H,1-5H3\"\nPentane,-3.18,CCCCC,[C][C][C][C][C],\"InChI=1S/C5H12/c1-3-5-4-2/h3-5H2,1-2H3\"\nPentobarbital,-2.39,O=C1NC(=O)NC(=O)C1(CC)C(C)CCC,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C][C],\"InChI=1S/C11H18N2O3/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\"\nPentyl acetate,-1.89,CCCCCOC(=O)C,[C][C][C][C][C][O][C][=Branch1][C][=O][C],\"InChI=1S/C7H14O2/c1-3-4-5-6-9-7(2)8/h3-6H2,1-2H3\"\nPentyl propanoate,-2.25,CCCCC(=O)OCC,[C][C][C][C][C][=Branch1][C][=O][O][C][C],\"InChI=1S/C7H14O2/c1-3-5-6-7(8)9-4-2/h3-6H2,1-2H3\"\nPentylbenzene,-4.64,CCCCCc1ccccc1,[C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C11H16/c1-2-3-5-8-11-9-6-4-7-10-11/h4,6-7,9-10H,2-3,5,8H2,1H3\"\nPentylcyclopentane,-6.08,CCCCCC1CCCC1,[C][C][C][C][C][C][C][C][C][C][Ring1][Branch1],\"InChI=1S/C10H20/c1-2-3-4-7-10-8-5-6-9-10/h10H,2-9H2,1H3\"\nPerfluidone,-3.8,Cc1cc(ccc1NS(=O)(=O)C(F)(F)F)S(=O)(=O)c2ccccc2,[C][C][=C][C][=Branch2][Ring1][=Branch1][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C14H12F3NO4S2/c1-10-9-12(23(19,20)11-5-3-2-4-6-11)7-8-13(10)18-24(21,22)14(15,16)17/h2-9,18H,1H3\"\nPermethrin,-6.291,CC1(C)C(C=C(Cl)Cl)C1C(=O)OCc2cccc(Oc3ccccc3)c2,[C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N],\"InChI=1S/C21H20Cl2O3/c1-21(2)17(12-18(22)23)19(21)20(24)25-13-14-7-6-10-16(11-14)26-15-8-4-3-5-9-15/h3-12,17,19H,13H2,1-2H3\"\nPerylene,-8.804,c1cc2cccc3c4cccc5cccc(c(c1)c23)c54,[C][=C][C][=C][C][=C][C][C][=C][C][=C][C][=C][C][=C][C][Branch1][=N][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=Ring1][=N][=C][Ring1][=Branch2][Ring1][=N],InChI=1S/C20H12/c1-5-13-6-2-11-17-18-12-4-8-14-7-3-10-16(20(14)18)15(9-1)19(13)17/h1-12H\np-Fluoroacetanilide,-1.78,CC(=O)Nc1ccc(F)cc1,[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"InChI=1S/C8H8FNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\"\nPhenacetin,-2.35,CCOc1ccc(NC(=O)C)cc1,[C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2],\"InChI=1S/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12)\"\nPhenanthrene,-5.26,c1ccc2c(c1)ccc3ccccc32,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][O],InChI=1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H\nPhenetole,-2.33,CCOc1ccccc1,[C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3\"\nPhenmedipham,-4.805,COC(=O)Nc1cccc(OC(=O)Nc2cccc(C)c2)c1,[C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][=C][Ring1][P],\"InChI=1S/C16H16N2O4/c1-11-5-3-6-12(9-11)18-16(20)22-14-8-4-7-13(10-14)17-15(19)21-2/h3-10H,1-2H3,(H,17,19)(H,18,20)\"\nPhenol,0,c1ccccc1O,[C][=C][C][=C][C][=C][Ring1][=Branch1][O],\"InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H\"\nPhenylhydrazine,0.07,NNc1ccccc1,[N][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C6H8N2/c7-8-6-4-2-1-3-5-6/h1-5,8H,7H2\"\nPhenylmethanol,-0.4,OCc1ccccc1,[O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2\"\nPhenylthiourea,-1.77,NC(=S)Nc1ccccc1,[N][C][=Branch1][C][=S][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)\"\nPhenytoin,-4.097,O=C1NC(=O)C(N1)(c2ccccc2)c3ccccc3,[O][=C][N][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C15H12N2O2/c18-13-15(17-14(19)16-13,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H2,16,17,18,19)\"\nPhorate,-4.11,CCOP(=S)(OCC)SCSCC,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][C],\"InChI=1S/C7H17O2PS3/c1-4-8-10(11,9-5-2)13-7-12-6-3/h4-7H2,1-3H3\"\nPhosalone,-5.233,CCOP(=S)(OCC)SCn1c(=O)oc2cc(Cl)ccc12,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1],\"InChI=1S/C12H15ClNO4PS2/c1-3-16-19(20,17-4-2)21-8-14-10-6-5-9(13)7-11(10)18-12(14)15/h5-7H,3-4,8H2,1-2H3\"\nPhoxim,-4.862,CCOP(=S)(OCC)ON=C(C#N)c1ccccc1,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][N][=C][Branch1][Ring1][C][#N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H15N2O3PS/c1-3-15-18(19,16-4-2)17-14-12(10-13)11-8-6-5-7-9-11/h5-9H,3-4H2,1-2H3\"\nphthalamide,-2.932,c1cC2C(=O)NC(=O)C2cc1,[C][=C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][#Branch1][C][=C][Ring1][O],\"InChI=1S/C8H7NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-6H,(H,9,10,11)\"\nPhthalonitrile,-2.38,N#Cc1ccccc1C#N,[N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][#N],InChI=1S/C8H4N2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H\np-Hydroxyacetanilide,-1.03,CC(=O)Nc1ccc(O)cc1,[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)\"\np-Hydroxybenzaldehyde ,-0.96,Oc1ccc(C=O)cc1,[O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2],\"InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H\"\nPicene,-7.87,c1ccc2c(c1)ccc3c2ccc4c5ccccc5ccc43,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][Ring1][=C],InChI=1S/C22H14/c1-3-7-17-15(5-1)9-11-21-19(17)13-14-20-18-8-4-2-6-16(18)10-12-22(20)21/h1-14H\nPiperine,-3.46,O=C(C=CC=Cc2ccc1OCOc1c2)N3CCCCC3,[O][=C][Branch2][Ring1][C][C][=C][C][=C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1],\"InChI=1S/C17H19NO3/c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15/h2-3,6-9,12H,1,4-5,10-11,13H2\"\nPiperophos,-4.15,CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C,[C][C][C][O][P][=Branch1][C][=S][Branch1][Branch1][O][C][C][C][S][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][C],\"InChI=1S/C14H28NO3PS2/c1-4-10-17-19(20,18-11-5-2)21-12-14(16)15-9-7-6-8-13(15)3/h13H,4-12H2,1-3H3\"\nPirimicarb,-1.95,CN(C)C(=O)Oc1nc(nc(C)c1C)N(C)C,[C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=N][C][=Branch1][#Branch2][=N][C][Branch1][C][C][=C][Ring1][#Branch1][C][N][Branch1][C][C][C],InChI=1S/C11H18N4O2/c1-7-8(2)12-10(14(3)4)13-9(7)17-11(16)15(5)6/h1-6H3\np-Methoxybenzaldehyde,-1.49,COc1ccc(C=O)cc1,[C][O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2],\"InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3\"\np-Methylaniline ,-1.21,Cc1ccc(N)cc1,[C][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3\"\np-Nitroaniline,-2.37,Nc1ccc(cc1)N(=O)=O,[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H2\"\np-Nitroanisole,-2.41,COc1ccc(cc1)N(=O)=O,[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C7H7NO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3\"\np-Nitrophenol,-0.74,Oc1ccc(cc1)N(=O)=O,[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H\"\np-Nitrotoluene,-2.49,Cc1ccc(cc1)N(=O)=O,[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O],\"InChI=1S/C7H7NO2/c1-6-2-4-7(5-3-6)8(9)10/h2-5H,1H3\"\np-Phenylphenol,-3.48,Oc1ccc(cc1)c2ccccc2,[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H10O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,13H\"\nPrasterone,-4.12,CC34CCC1C(CC=C2CC(O)CCC12C)C3CCC4=O,[C][C][C][C][C][C][Branch1][P][C][C][=C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O],\"InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3\"\nPrednisolone,-3.18,CC12CC(O)C3C(CCC4=CC(=O)C=CC34C)C2CCC1(O)C(=O)CO,[C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O],\"InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h5,7,9,14-16,18,22,24,26H,3-4,6,8,10-11H2,1-2H3\"\nPrimidone,-2.64,CCC1(C(=O)NCNC1=O)c2ccccc2,[C][C][C][Branch1][N][C][=Branch1][C][=O][N][C][N][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C12H14N2O2/c1-2-12(9-6-4-3-5-7-9)10(15)13-8-14-11(12)16/h3-7H,2,8H2,1H3,(H,13,15)(H,14,16)\"\nProcymidone,-4.8,CC12CC2(C)C(=O)N(C1=O)c3cc(Cl)cc(Cl)c3,[C][C][C][C][Ring1][Ring1][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][Branch2][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C13H11Cl2NO2/c1-12-6-13(12,2)11(18)16(10(12)17)9-4-7(14)3-8(15)5-9/h3-5H,6H2,1-2H3\"\nProgesterone,-4.42,CC(=O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C,[C][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring2][Ring1][Ring1][Ring1][S][C],\"InChI=1S/C21H30O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12,16-19H,4-11H2,1-3H3\"\nPrometon,-2.478,COc1nc(NC(C)C)nc(NC(C)C)n1,[C][O][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C],\"InChI=1S/C10H19N5O/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\"\nPrometryn,-4.1,CSc1nc(NC(C)C)nc(NC(C)C)n1,[C][S][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C],\"InChI=1S/C10H19N5S/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\"\nPropane,-1.94,CCC,[C][C][C],\"InChI=1S/C3H8/c1-3-2/h3H2,1-2H3\"\nPropanil,-3,CCC(=O)Nc1ccc(Cl)c(Cl)c1,[C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C9H9Cl2NO/c1-2-9(13)12-6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3,(H,12,13)\"\nPropazine,-4.43,CC(C)Nc1nc(Cl)nc(NC(C)C)n1,[C][C][Branch1][C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O],\"InChI=1S/C9H16ClN5/c1-5(2)11-8-13-7(10)14-9(15-8)12-6(3)4/h5-6H,1-4H3,(H2,11,12,13,14,15)\"\nPropetamphos,-3.408,CCNP(=S)(OC)OC(=CC(=O)OC(C)C)C,[C][C][N][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=Branch1][N][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C][C],\"InChI=1S/C10H20NO4PS/c1-6-11-16(17,13-5)15-9(4)7-10(12)14-8(2)3/h7-8H,6H2,1-5H3,(H,11,17)\"\nPropiconazole,-3.493,CCCC1COC(Cn2cncn2)(O1)c3ccc(Cl)cc3Cl,[C][C][C][C][C][O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][Ring2][O][Ring1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl],\"InChI=1S/C15H17Cl2N3O2/c1-2-3-12-7-21-15(22-12,8-20-10-18-9-19-20)13-5-4-11(16)6-14(13)17/h4-6,9-10,12H,2-3,7-8H2,1H3\"\nPropionaldehyde,0.58,CCC=O,[C][C][C][=O],\"InChI=1S/C3H6O/c1-2-3-4/h3H,2H2,1H3\"\nPropionitrile,0.28,CCC#N,[C][C][C][#N],\"InChI=1S/C3H5N/c1-2-3-4/h2H2,1H3\"\nPropoxur,-2.05,CNC(=O)Oc1ccccc1OC(C)C,[C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Branch1][C][C][C],\"InChI=1S/C11H15NO3/c1-8(2)14-9-6-4-5-7-10(9)15-11(13)12-3/h4-8H,1-3H3,(H,12,13)\"\nPropyl acetate,-0.72,CCCOC(=O)C,[C][C][C][O][C][=Branch1][C][=O][C],\"InChI=1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3\"\nPropyl butyrate,-1.92,CCCC(=O)OC,[C][C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C5H10O2/c1-3-4-5(6)7-2/h3-4H2,1-2H3\"\nPropyl formate,-0.49,CCCOC=O,[C][C][C][O][C][=O],\"InChI=1S/C4H8O2/c1-2-3-6-4-5/h4H,2-3H2,1H3\"\nPropyl propanoate,-1.34,CCCCC(=O)OC,[C][C][C][C][C][=Branch1][C][=O][O][C],\"InChI=1S/C6H12O2/c1-3-4-5-6(7)8-2/h3-5H2,1-2H3\"\nPropylbenzene ,-3.37,CCCc1ccccc1,[C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C9H12/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3\"\nPropylcyclopentane,-4.74,CCCC1CCCC1,[C][C][C][C][C][C][C][C][Ring1][Branch1],\"InChI=1S/C8H16/c1-2-5-8-6-3-4-7-8/h8H,2-7H2,1H3\"\nPropylene,-1.08,CC=C,[C][C][=C],\"InChI=1S/C3H6/c1-3-2/h3H,1H2,2H3\"\nPropylisopropylether,-1.34,CCCOC(C)C,[C][C][C][O][C][Branch1][C][C][C],\"InChI=1S/C6H14O/c1-4-5-7-6(2)3/h6H,4-5H2,1-3H3\"\nPropyne,-0.41,CC#C,[C][C][#C],\"InChI=1S/C3H4/c1-3-2/h1H,2H3\"\np-t-Butylphenol,-2.41,CC(C)(C)c1ccc(O)cc1,[C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],\"InChI=1S/C10H14O/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3\"\nPteridine,0.02,c2cnc1ncncc1n2,[C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2],InChI=1S/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H\np-terphenyl,-7.11,c1ccc(cc1)c2ccc(cc2)c3ccccc3,[C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],InChI=1S/C18H14/c1-3-7-15(8-4-1)17-11-13-18(14-12-17)16-9-5-2-6-10-16/h1-14H\np-Toluenesulfonamide ,-1.74,Cc1ccc(cc1)S(=O)(=O)N,[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N],\"InChI=1S/C7H9NO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)\"\np-Xylene ,-2.77,Cc1ccc(C)cc1,[C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],\"InChI=1S/C8H10/c1-7-3-5-8(2)6-4-7/h3-6H,1-2H3\"\nPyrazinamide,-0.667,NC(=O)c1cnccn1,[N][C][=Branch1][C][=O][C][=C][N][=C][C][=N][Ring1][=Branch1],\"InChI=1S/C5H5N3O/c6-5(9)4-3-7-1-2-8-4/h1-3H,(H2,6,9)\"\nPyrazon,-2.878,Nc2cnn(c1ccccc1)c(=O)c2Cl,[N][C][C][=N][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Ring1][=N][Cl],\"InChI=1S/C10H8ClN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\"\nPyrene,-6.176,c1cc2ccc3cccc4ccc(c1)c2c34,[C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1],InChI=1S/C16H10/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h1-10H\nPyridazine,1.1,c1ccnnc1,[C][=C][C][=N][N][=C][Ring1][=Branch1],InChI=1S/C4H4N2/c1-2-4-6-5-3-1/h1-4H\nPyridine,0.76,c1ccncc1,[C][=C][C][=N][C][=C][Ring1][=Branch1],InChI=1S/C5H5N/c1-2-4-6-5-3-1/h1-5H\nPyrimidine,1.1,c1cncnc1,[C][=C][N][=C][N][=C][Ring1][=Branch1],InChI=1S/C4H4N2/c1-2-5-4-6-3-1/h1-4H\nPyrolan,-2.09,CN(C)C(=O)Oc1cc(C)nn1c2ccccc2,[C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C13H15N3O2/c1-10-9-12(18-13(17)15(2)3)16(14-10)11-7-5-4-6-8-11/h4-9H,1-3H3\"\nQuinethazone,-3.29,CCC2NC(=O)c1cc(c(Cl)cc1N2)S(N)(=O)=O,[C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][N][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][N][S][Branch1][C][N][=Branch1][C][=O][=O],\"InChI=1S/C10H12ClN3O3S/c1-2-9-13-7-4-6(11)8(18(12,16)17)3-5(7)10(15)14-9/h3-4,9,13H,2H2,1H3,(H,14,15)(H2,12,16,17)\"\nQuinoline,-1.3,c1ccc2ncccc2c1,[C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],InChI=1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H\nQuinonamid,-5.03,ClC(Cl)CC(=O)NC2=C(Cl)C(=O)c1ccccc1C2=O,[Cl][C][Branch1][C][Cl][C][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=O],\"InChI=1S/C13H8Cl3NO3/c14-8(15)5-9(18)17-11-10(16)12(19)6-3-1-2-4-7(6)13(11)20/h1-4,8H,5H2,(H,17,18)\"\nQuintozene,-5.82,Clc1c(Cl)c(Cl)c(N(=O)=O)c(Cl)c1Cl,[Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][N][Cl],InChI=1S/C6Cl5NO2/c7-1-2(8)4(10)6(12(13)14)5(11)3(1)9\nRaffinose,-0.41,OCC1OC(CO)(OC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)C(O)C1O,[O][C][C][O][C][Branch1][Ring1][C][O][Branch2][Ring2][#Branch2][O][C][O][C][Branch2][Ring1][=Branch1][C][O][C][O][C][Branch1][Ring1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Branch1][O][C][Branch1][C][O][C][Ring2][Ring1][#C][O],\"InChI=1S/C18H32O16/c19-1-5-8(22)11(25)13(27)16(31-5)30-3-7-9(23)12(26)14(28)17(32-7)34-18(4-21)15(29)10(24)6(2-20)33-18/h5-17,19-29H,1-4H2\"\nReposal,-2.696,CCC1(C(=O)NC(=O)NC1=O)C2=CCC3CCC2C3,[C][C][C][Branch1][#C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][Branch2][=O][C][=C][C][C][C][C][C][Ring1][#Branch1][C][Ring1][Branch1],\"InChI=1S/C14H18N2O3/c1-2-14(11(17)15-13(19)16-12(14)18)10-6-4-8-3-5-9(10)7-8/h6,8-9H,2-5,7H2,1H3,(H2,15,16,17,18,19)\"\nrhodanine,-1.77,C1SC(=S)NC1(=O),[C][S][C][=Branch1][C][=S][N][C][Ring1][=Branch1][=O],\"InChI=1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)\"\nRiboflavin,-3.685,Cc3cc2nc1c(=O)[nH]c(=O)nc1n(CC(O)C(O)C(O)CO)c2cc3C,[C][C][=C][C][N][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=O][N][=C][Ring1][Branch2][N][Branch1][S][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O][C][=Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][=Branch2][C],\"InChI=1S/C17H20N4O6/c1-7-3-9-10(4-8(7)2)21(5-11(23)14(25)12(24)6-22)15-13(18-9)16(26)20-17(27)19-15/h3-4,11-12,14,22-25H,5-6H2,1-2H3,(H,20,26,27)\"\nRisocaine,-2.452,CCCOC(=O)c1ccc(N)cc1,[C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"InChI=1S/C10H13NO2/c1-2-7-13-10(12)8-3-5-9(11)6-4-8/h3-6H,2,7,11H2,1H3\"\nRonnel,-5.72,COP(=S)(OC)Oc1cc(Cl)c(Cl)cc1Cl,[C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl],\"InChI=1S/C8H8Cl3O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\"\nRovral,-4.376,CC(C)NC(=O)N1CC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2,[C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2],\"InChI=1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)\"\nSalicin,-0.85,OCC2OC(Oc1ccccc1CO)C(O)C(O)C2O,[O][C][C][O][C][Branch1][N][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][P][O],\"InChI=1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2\"\nSalicylamide,-1.836,NC(=O)c1ccccc1O,[N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O],\"InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\"\nsalicylanilide,-3.59,c1ccccc1NC(=O)c2c(O)cccc2,[C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][C][=C][Ring1][#Branch1],\"InChI=1S/C13H11NO2/c15-12-9-5-4-8-11(12)13(16)14-10-6-2-1-3-7-10/h1-9,15H,(H,14,16)\"\nSantonin,-3.09,CC3C2CCC1(C)C=CC(=O)C(=C1C2OC3=O)C,[C][C][C][C][C][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=Branch1][N][=C][Ring1][Branch2][C][Ring1][N][O][C][Ring1][#C][=O][C],\"InChI=1S/C15H18O3/c1-8-10-4-6-15(3)7-5-11(16)9(2)12(15)13(10)18-14(8)17/h5,7-8,10,13H,4,6H2,1-3H3\"\nSecobarbital,-2.356,O=C1NC(=O)NC(=O)C1(C(C)CCC)CC=C,[O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Branch2][C][Branch1][C][C][C][C][C][C][C][=C],\"InChI=1S/C12H18N2O3/c1-4-6-8(3)12(7-5-2)9(15)13-11(17)14-10(12)16/h5,8H,2,4,6-7H2,1,3H3,(H2,13,14,15,16,17)\"\nSiduron,-4.11,CC1CCCCC1NC(=O)Nc2ccccc2,[C][C][C][C][C][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C14H20N2O/c1-11-7-5-6-10-13(11)16-14(17)15-12-8-3-2-4-9-12/h2-4,8-9,11,13H,5-7,10H2,1H3,(H2,15,16,17)\"\nSimetryn,-2.676,CSc1nc(nc(n1)N(C)C)N(C)C,[C][S][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C],InChI=1S/C8H15N5S/c1-12(2)6-9-7(13(3)4)11-8(10-6)14-5/h1-5H3\nSorbitol,1.09,OCC(O)C(O)C(O)C(O)CO,[O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O],\"InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2\"\n\"Sparsomycin (3,8mg/ml)\",-1.981,CSCS(=O)CC(CO)NC(=O)C=Cc1c(C)[nH]c(=O)[nH]c1=O,[C][S][C][S][=Branch1][C][=O][C][C][Branch1][Ring1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][NH1][C][=Branch1][C][=O][NH1][C][Ring1][Branch2][=O],\"InChI=1S/C13H19N3O5S2/c1-8-10(12(19)16-13(20)14-8)3-4-11(18)15-9(5-17)6-23(21)7-22-2/h3-4,9,17H,5-7H2,1-2H3,(H,15,18)(H2,14,16,19,20)\"\nSpironolactone,-4.173,CC(=O)SC4CC1=CC(=O)CCC1(C)C5CCC2(C)C(CCC23CCC(=O)O3)C45,[C][C][=Branch1][C][=O][S][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][C][C][C][Branch1][C][C][C][Branch1][#C][C][C][C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][O][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][Ring1][#C],\"InChI=1S/C24H32O4S/c1-14(25)29-19-13-15-12-16(26)4-8-22(15,2)17-5-9-23(3)18(21(17)19)6-10-24(23)11-7-20(27)28-24/h12,17-19,21H,4-11,13H2,1-3H3\"\nStirofos,-4.522,COP(=O)(OC)OC(=CCl)c1cc(Cl)c(Cl)cc1Cl,[C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][=Branch1][Ring1][=C][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl],\"InChI=1S/C10H9Cl4O4P/c1-16-19(15,17-2)18-10(5-11)6-3-8(13)9(14)4-7(6)12/h3-5H,1-2H3\"\nStyrene,-2.82,C=Cc1ccccc1,[C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H2\"\nSuccinimide,0.3,O=C1CCC(=O)N1,[O][=C][C][C][C][=Branch1][C][=O][N][Ring1][=Branch1],\"InChI=1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)\"\nSulfallate,-3.39,CCN(CC)C(=S)SCC(Cl)=C,[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][C][C][Branch1][C][Cl][=C],\"InChI=1S/C8H14ClNS2/c1-4-10(5-2)8(11)12-6-7(3)9/h3-6H2,1-2H3\"\nSulfanilamide,-1.34,Nc1ccc(cc1)S(N)(=O)=O,[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][Branch1][C][N][=Branch1][C][=O][=O],\"InChI=1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)\"\nTalbutal,-2.016,CCC(C)C1(CC=C)C(=O)NC(=O)NC1=O,[C][C][C][Branch1][C][C][C][Branch1][Ring2][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][O][=O],\"InChI=1S/C11H16N2O3/c1-4-6-11(7(3)5-2)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16)\"\nt-Butylbenzene ,-3.66,CC(C)(C)c1ccccc1,[C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C10H14/c1-10(2,3)9-7-5-4-6-8-9/h4-8H,1-3H3\"\nt-Crotonaldehyde,0.32,C/C=C/C=O,[C][/C][=C][/C][=O],\"InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3/b3-2+\"\nTerbacil,-2.484,Cc1[nH]c(=O)n(c(=O)c1Cl)C(C)(C)C,[C][C][NH1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=Branch1][C][=O][C][=Ring1][Branch2][Cl][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C9H13ClN2O2/c1-5-6(10)7(13)12(8(14)11-5)9(2,3)4/h1-4H3,(H,11,14)\"\nTerbufos,-4.755,CCOP(=S)(OCC)SCSC(C)(C)C,[C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][Branch1][C][C][Branch1][C][C][C],\"InChI=1S/C9H21O2PS3/c1-6-10-12(13,11-7-2)15-8-14-9(3,4)5/h6-8H2,1-5H3\"\nTerbumeton,-3.239,CCNc1nc(NC(C)(C)C)nc(OC)n1,[C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][=N],\"InChI=1S/C10H19N5O/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\"\nTerbutryn,-4,CCNc1nc(NC(C)(C)C)nc(SC)n1,[C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][=N],\"InChI=1S/C10H19N5S/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\"\nTestosterone,-4.02,CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1O,[C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O],\"InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3\"\nTetrabromomethane,-3.14,BrC(Br)(Br)Br,[Br][C][Branch1][C][Br][Branch1][C][Br][Br],\"InChI=1S/CBr4/c2-1(3,4)5\"\nTetrachloroethylene,-2.54,ClC(=C(Cl)Cl)Cl,[Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl],InChI=1S/C2Cl4/c3-1(4)2(5)6\nTetrachloromethane,-2.31,ClC(Cl)(Cl)Cl,[Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/CCl4/c2-1(3,4)5\"\nTetradecane,-7.96,CCCCCCCCCCCCCC,[C][C][C][C][C][C][C][C][C][C][C][C][C][C],\"InChI=1S/C14H30/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3-14H2,1-2H3\"\nTetrafluthrin,-7.321,Cc1c(F)c(F)c(COC(=O)C2C(C=C(Cl)C(F)(F)F)C2(C)C)c(F)c1F,[C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Branch2][Ring1][#C][C][O][C][=Branch1][C][=O][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][#Branch2][Branch1][C][C][C][C][Branch1][C][F][=C][Ring2][Ring1][=Branch2][F],\"InChI=1S/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3\"\nTetrahydrofurane ,0.49,C1CCOC1,[C][C][C][O][C][Ring1][Branch1],InChI=1S/C4H8O/c1-2-4-5-3-1/h1-4H2\nTetrahydropyran ,-0.03,C1CCOCC1,[C][C][C][O][C][C][Ring1][=Branch1],InChI=1S/C5H10O/c1-2-4-6-5-3-1/h1-5H2\nThalidomide,-2.676,O=C1N(C2CCC(=O)NC2=O)C(=O)c3ccccc13,[O][=C][N][Branch1][=N][C][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1],\"InChI=1S/C13H10N2O4/c16-10-6-5-9(11(17)14-10)15-12(18)7-3-1-2-4-8(7)13(15)19/h1-4,9H,5-6H2,(H,14,16,17)\"\nTheophylline,-1.39,Cn1c(=O)n(C)c2nc[nH]c2c1=O,[C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][NH1][C][=Ring1][Branch1][C][Ring1][O][=O],\"InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)\"\nthioanisole,-2.39,c1ccccc1SC,[C][=C][C][=C][C][=C][Ring1][=Branch1][S][C],\"InChI=1S/C7H8S/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\"\nThiometon,-3.091,CCSCCSP(=S)(OC)OC,[C][C][S][C][C][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C],\"InChI=1S/C6H15O2PS3/c1-4-11-5-6-12-9(10,7-2)8-3/h4-6H2,1-3H3\"\nThiophene,-1.33,c1ccsc1,[C][C][=C][S][C][=Ring1][Branch1],InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H\nThiophenol ,-2.12,Sc1ccccc1,[S][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C6H6S/c7-6-4-2-1-3-5-6/h1-5,7H\"\nThiourea,0.32,NC(=S)N,[N][C][=Branch1][C][=S][N],\"InChI=1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)\"\nThymol,-2.22,CC(C)c1ccc(C)cc1O,[C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][O],\"InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-7,11H,1-3H3\"\nToluene ,-2.21,Cc1ccccc1,[C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3\"\nt-Pentylbenzene,-4.15,CC(C)(C)Cc1ccccc1,[C][C][Branch1][C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"InChI=1S/C11H16/c1-11(2,3)9-10-7-5-4-6-8-10/h4-8H,9H2,1-3H3\"\n\"trans-1,4-Dimethylcyclohexane\",-4.47,C/C1CCC(\\C)CC1,[C][/C][C][C][C][Branch1][C][\\C][C][C][Ring1][#Branch1],\"InChI=1S/C8H16/c1-7-3-5-8(2)6-4-7/h7-8H,3-6H2,1-2H3\"\ntrans-2-Heptene ,-3.82,CCCC/C=C/C,[C][C][C][C][/C][=C][/C],\"InChI=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+\"\ntrans-2-Pentene ,-2.54,CC/C=C/C,[C][C][/C][=C][/C],\"InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3+\"\nTriadimefon,-3.61,CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)n2cncn2,[C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=N][C][=N][Ring1][Branch1],\"InChI=1S/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3\"\nTriallate,-4.88,CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl,[C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][Branch1][C][Cl][=C][Branch1][C][Cl][Cl],\"InChI=1S/C10H16Cl3NOS/c1-6(2)14(7(3)4)10(15)16-5-8(11)9(12)13/h6-7H,5H2,1-4H3\"\nTriamcinolone,-3.68,CC34CC(O)C1(F)C(CCC2=CC(=O)C=CC12C)C3CC(O)C4(O)C(=O)CO,[C][C][C][C][Branch1][C][O][C][Branch1][C][F][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][N][Ring1][#Branch1][C][C][Ring2][Ring1][C][C][C][Branch1][C][O][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O],\"InChI=1S/C21H27FO6/c1-18-6-5-12(24)7-11(18)3-4-13-14-8-15(25)21(28,17(27)10-23)19(14,2)9-16(26)20(13,18)22/h5-7,13-16,23,25-26,28H,3-4,8-10H2,1-2H3\"\nTriamterene,-2.404,Nc3nc(N)c2nc(c1ccccc1)c(N)nc2n3,[N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][N][=N][C][Ring1][=N][=N][Ring2][Ring1][C],\"InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)\"\nTriazolam,-4.09,Cc3nnc4CN=C(c1ccccc1Cl)c2cc(Cl)ccc2n34,[C][C][=N][N][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1],\"InChI=1S/C17H12Cl2N4/c1-10-21-22-16-9-20-17(12-4-2-3-5-14(12)19)13-8-11(18)6-7-15(13)23(10)16/h2-8H,9H2,1H3\"\nTribromomethane,-1.91,BrC(Br)Br,[Br][C][Branch1][C][Br][Br],InChI=1S/CHBr3/c2-1(3)4/h1H\nTrichlorfon,-0.22,COP(=O)(OC)C(O)C(Cl)(Cl)Cl,[C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][C][Branch1][C][O][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"InChI=1S/C4H8Cl3O4P/c1-10-12(9,11-2)3(8)4(5,6)7/h3,8H,1-2H3\"\nTrichloroacetonitrile,-2.168,ClC(Cl)(Cl)C#N,[Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][#N],\"InChI=1S/C2Cl3N/c3-2(4,5)1-6\"\nTrichloroethylene,-1.96,ClC=C(Cl)Cl,[Cl][C][=C][Branch1][C][Cl][Cl],InChI=1S/C2HCl3/c3-1-2(4)5/h1H\nTrichloromethane,-1.17,ClC(Cl)Cl,[Cl][C][Branch1][C][Cl][Cl],InChI=1S/CHCl3/c2-1(3)4/h1H\nTrichloronate,-5.752,CCOP(=S)(CC)Oc1cc(Cl)c(Cl)cc1Cl,[C][C][O][P][=Branch1][C][=S][Branch1][Ring1][C][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl],\"InChI=1S/C10H12Cl3O2PS/c1-3-14-16(17,4-2)15-10-6-8(12)7(11)5-9(10)13/h5-6H,3-4H2,1-2H3\"\nTriclosan,-4.46,Oc1cc(Cl)ccc1Oc2ccc(Cl)cc2Cl,[O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl],\"InChI=1S/C12H7Cl3O2/c13-7-1-3-11(9(15)5-7)17-12-4-2-8(14)6-10(12)16/h1-6,16H\"\nTricresyl phosphate,-6.01,Cc1ccc(OP(=O)(Oc2cccc(C)c2)Oc3ccccc3C)cc1,[C][C][=C][C][=C][Branch2][Ring1][=C][O][P][=Branch1][C][=O][Branch1][=N][O][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][Ring2][Ring1][=Branch2],\"InChI=1S/C21H21O4P/c1-16-11-13-19(14-12-16)23-26(22,24-20-9-6-7-17(2)15-20)25-21-10-5-4-8-18(21)3/h4-15H,1-3H3\"\nTrietazine,-4.06,CCNc1nc(Cl)nc(n1)N(CC)CC,[C][C][N][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C],\"InChI=1S/C9H16ClN5/c1-4-11-8-12-7(10)13-9(14-8)15(5-2)6-3/h4-6H2,1-3H3,(H,11,12,13,14)\"\nTriethyl phosphate,0.43,CCOP(=O)(OCC)OCC,[C][C][O][P][=Branch1][C][=O][Branch1][Ring2][O][C][C][O][C][C],\"InChI=1S/C6H15O4P/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3\"\nTrifluralin,-5.68,CCCN(CCC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O,[C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O],\"InChI=1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\"\nTriphenylene,-6.726,c1ccc2c(c1)c3ccccc3c4ccccc24,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],InChI=1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H\nUrea,0.96,NC(=O)N,[N][C][=Branch1][C][=O][N],\"InChI=1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)\"\nValeraldehyde,-0.85,CCCCC=O,[C][C][C][C][C][=O],\"InChI=1S/C5H10O/c1-2-3-4-5-6/h5H,2-4H2,1H3\"\nvamidothion,1.144,CNC(=O)C(C)SCCSP(=O)(OC)(OC),[C][N][C][=Branch1][C][=O][C][Branch1][C][C][S][C][C][S][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C],\"InChI=1S/C8H18NO4PS2/c1-7(8(10)9-2)15-5-6-16-14(11,12-3)13-4/h7H,5-6H2,1-4H3,(H,9,10)\"\nVinclozolin,-4.925,CC1(OC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2)C=C,[C][C][Branch2][Ring1][O][O][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C],\"InChI=1S/C12H9Cl2NO3/c1-3-12(2)10(16)15(11(17)18-12)9-5-7(13)4-8(14)6-9/h3-6H,1H2,2H3\"\nXipamide,-3.79,Cc1cccc(C)c1NC(=O)c2cc(c(Cl)cc2O)S(N)(=O)=O,[C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][O][S][Branch1][C][N][=Branch1][C][=O][=O],\"InChI=1S/C15H15ClN2O4S/c1-8-4-3-5-9(2)14(8)18-15(20)10-6-13(23(17,21)22)11(16)7-12(10)19/h3-7,19H,1-2H3,(H,18,20)(H2,17,21,22)\"\nXMC,-2.581,CNC(=O)Oc1cc(C)cc(C)c1,[C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2],\"InChI=1S/C10H13NO2/c1-7-4-8(2)6-9(5-7)13-10(12)11-3/h4-6H,1-3H3,(H,11,12)\"\n"
  },
  {
    "path": "dataset/ESOL/ESOL.json",
    "content": "[\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" p-Cresol\\n\",\n        \"output\": \" Cc1ccc(O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methy-2-Butene\\n\",\n        \"output\": \" [C][C][=C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCC(O)(CC)CC\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" alloxantin\\n\",\n        \"output\": \" C1(=O)NC(=O)NC(=O)C1(O)C2(O)C(=O)NC(=O)NC2(=O)\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" DDD\\n\",\n        \"output\": \" InChI=1S/C14H10Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8,13-14H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2,4,5-Tetrabromobenzene\\n\",\n        \"output\": \" [Br][C][=C][C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,4,6-Trimethylphenol\\n\",\n        \"output\": \" InChI=1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Tetrachloromethane\\n\",\n        \"output\": \" InChI=1S/CCl4/c2-1(3,4)5\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][=C][Ring1][P]\\n\",\n        \"output\": \" Phenmedipham\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C18H32O16/c19-1-5-8(22)11(25)13(27)16(31-5)30-3-7-9(23)12(26)14(28)17(32-7)34-18(4-21)15(29)10(24)6(2-20)33-18/h5-17,19-29H,1-4H2\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Etomidate\\n\",\n        \"output\": \" InChI=1S/C14H16N2O2/c1-3-18-14(17)13-9-15-10-16(13)11(2)12-7-5-4-6-8-12/h4-11H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)C)C(C)C\\n\",\n        \"output\": \" 5,5-Diisopropylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][Br]\\n\",\n        \"output\": \" 0.16218100973589297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C21H22N2O4/c1-2-3-14-18(24)27-15-23-19(25)21(22-20(23)26,16-10-6-4-7-11-16)17-12-8-5-9-13-17/h4-13H,2-3,14-15H2,1H3,(H,22,26)\\n\",\n        \"output\": \" 2.0989398836235246e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,2-Dimethylbutane\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCC(CC)C=O\\n\",\n        \"output\": \" 2-Ethylhexanal\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" -2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Butanethiol \\n\",\n        \"output\": \" InChI=1S/C4H10S/c1-2-3-4-5/h5H,2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzocaine\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Xipamide\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][O][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C(C=CC=Cc2ccc1OCOc1c2)N3CCCCC3\\n\",\n        \"output\": \" Piperine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)CCOC(=O)C\\n\",\n        \"output\": \" Isopentyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CNC(=O)Oc1ccccc1OC(C)C\\n\",\n        \"output\": \" Propoxur\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCNc1nc(NC(C)(C)C)nc(OC)n1\\n\",\n        \"output\": \" Terbumeton\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H5Cl7/c11-4-2-1-3-5(4)9(15)7(13)6(12)8(3,14)10(9,16)17/h1-5H\\n\",\n        \"output\": \" Heptachlor\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H7Cl/c8-6-7-4-2-1-3-5-7/h1-5H,6H2\\n\",\n        \"output\": \" Benzylchloride\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H34O3/c1-15(2)22-18(20)14-17(4)11-8-10-16(3)12-9-13-19(5,6)21-7/h8,11,14-16H,9-10,12-13H2,1-7H3\\n\",\n        \"output\": \" -5.19\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO\\n\",\n        \"output\": \" -3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC1(C)C2CCC1(C)C(=O)C2\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,2-Dimethyl-1-butanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.17\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Hexanone\\n\",\n        \"output\": \" [C][C][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,3,5-Trichlorobenzene\\n\",\n        \"output\": \" Clc1cc(Cl)cc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19)\\n\",\n        \"output\": \" -4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)\\n\",\n        \"output\": \" 0.016982436524617443 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5ClO/c7-5-2-1-3-6(8)4-5/h1-4,8H\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Chloropham\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COP(=S)(OC)Oc1cc(Cl)c(I)cc1Cl\\n\",\n        \"output\": \" Iodofenphos\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2,4-Dinitrotoluene\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H18N6/c1-13(2)7-10-8(14(3)4)12-9(11-7)15(5)6/h1-6H3\\n\",\n        \"output\": \" -3.364\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benznidazole\\n\",\n        \"output\": \" [O][=C][Branch1][=C][C][N][C][=C][N][=C][Ring1][Branch1][N][=Branch1][C][=O][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCS\\n\",\n        \"output\": \" Butanethiol \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" oryzalin\\n\",\n        \"output\": \" 6.9183097091893625e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.766\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chloroxuron\\n\",\n        \"output\": \" InChI=1S/C15H15ClN2O2/c1-18(2)15(19)17-12-5-9-14(10-6-12)20-13-7-3-11(16)4-8-13/h3-10H,1-2H3,(H,17,19)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H16O2/c1-3-5-6-7-8(9)10-4-2/h3-7H2,1-2H3\\n\",\n        \"output\": \" 0.0044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCN(CC)c1nc(Cl)nc(n1)N(CC)CC\\n\",\n        \"output\": \" -4.4110000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Triethyl phosphate\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Cl]\\n\",\n        \"output\": \" 1-Chloropropane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][#N]\\n\",\n        \"output\": \" Trichloroacetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1ccccc1C(O)c2ccccc2\\n\",\n        \"output\": \" benzhydrol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Phenanthrene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=Branch2][Ring1][=Branch1][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Bromohexane\\n\",\n        \"output\": \" [C][C][C][C][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Oc1c(Cl)cc(Cl)cc1Cl\\n\",\n        \"output\": \" -2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Pyrazon\\n\",\n        \"output\": \" InChI=1S/C10H8ClN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][C][C][C][=C]\\n\",\n        \"output\": \" 4-Pentene-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC1=C(Cl)C2(Cl)C3C4CC(C=C4)C3C1(Cl)C2(Cl)Cl\\n\",\n        \"output\": \" Aldrin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Phenylmethanol\\n\",\n        \"output\": \" OCc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Neburon\\n\",\n        \"output\": \" 1.698243652461746e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" m-Nitrophenol\\n\",\n        \"output\": \" Oc1cccc(c1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C][C]\\n\",\n        \"output\": \" Pentobarbital\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylpentane\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Mefluidide\\n\",\n        \"output\": \" 0.0005754399373371566 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C3H7NO2/c1-2-3-4(5)6/h2-3H2,1H3\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-3-4(2)5/h3H2,1-2H3\\n\",\n        \"output\": \" 3.311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Isobutylbenzene\\n\",\n        \"output\": \" 7.585775750291836e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Isofenphos\\n\",\n        \"output\": \" 6.397348354826482e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 9-Methylanthracene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" ClCC\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Propyl formate\\n\",\n        \"output\": \" 0.32359365692962827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Napthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 5-Ethyl-5-(3-methylbutyl)barbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)CCC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Cycloheptene\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15ClN4O6S/c1-3-26-14(22)10-6-4-5-7-11(10)27(23,24)19-20(9-21)15-17-12(16)8-13(18-15)25-2/h4-9,19H,3H2,1-2H3\\n\",\n        \"output\": \" Chlorimuron-ethyl (ph 7)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3\\n\",\n        \"output\": \" Tetrafluthrin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Pteridine\\n\",\n        \"output\": \" InChI=1S/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" benzhydrol\\n\",\n        \"output\": \" c1ccccc1C(O)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Barbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)CC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" borneol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][Branch1][C][O][C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Iodobenzene\\n\",\n        \"output\": \" InChI=1S/C6H5I/c7-6-4-2-1-3-5-6/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1CCCN1\\n\",\n        \"output\": \" 2-pyrrolidone\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H12N2O3/c1-2-8-13(9-6-4-3-5-7-9)10(16)14-12(18)15-11(13)17/h2-7H,1,8H2,(H2,14,15,16,17,18)\\n\",\n        \"output\": \" -2.369\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H19N5S/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" -4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H\\n\",\n        \"output\": \" benzhydrol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H30/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3-14H2,1-2H3\\n\",\n        \"output\": \" Tetradecane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propyne\\n\",\n        \"output\": \" InChI=1S/C3H4/c1-3-2/h1H,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2\\n\",\n        \"output\": \" Sorbitol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Glafenine\\n\",\n        \"output\": \" InChI=1S/C19H17ClN2O4/c20-12-5-6-14-17(7-8-21-18(14)9-12)22-16-4-2-1-3-15(16)19(25)26-11-13(24)10-23/h1-9,13,23-24H,10-11H2,(H,21,22)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H4Br2/c3-1-2-4/h1-2H2\\n\",\n        \"output\": \" -1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 3-Chloroanisole\\n\",\n        \"output\": \" -2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=Branch1][=N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 1,3,5-Trinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCl\\n\",\n        \"output\": \" 1-Chlorobutane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propionaldehyde\\n\",\n        \"output\": \" InChI=1S/C3H6O/c1-2-3-4/h3H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H10BrClN2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\",\n        \"output\": \" -3.924\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H3Cl3/c1-2(3,4)5/h1H3\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methocarbamol\\n\",\n        \"output\": \" InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Benzo[ghi]perylene\\n\",\n        \"output\": \" InChI=1S/C22H12/c1-3-13-7-9-15-11-12-16-10-8-14-4-2-6-18-17(5-1)19(13)21(15)22(16)20(14)18/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3\\n\",\n        \"output\": \" 2,6-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H8Cl2IO3PS/c1-12-15(16,13-2)14-8-4-5(9)7(11)3-6(8)10/h3-4H,1-2H3\\n\",\n        \"output\": \" Iodofenphos\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" COC(C)(C)C\\n\",\n        \"output\": \" -0.24\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Isocarboxazid\\n\",\n        \"output\": \" Cc1cc(no1)C(=O)NNCc2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClCBr\\n\",\n        \"output\": \" Bromochloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc2ncc1nccnc1n2\\n\",\n        \"output\": \" 2-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1cccc2ccccc12\\n\",\n        \"output\": \" 0.0001174897554939529 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 2,4,6-Trimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" 0.004677351412871981 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H27OPS3/c1-4-7-10-15-14(13,16-11-8-5-2)17-12-9-6-3/h4-12H2,1-3H3\\n\",\n        \"output\": \" DEF\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H6N2OS/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)\\n\",\n        \"output\": \" -2.436\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C11H16ClO2PS3/c1-3-13-15(16,14-4-2)18-9-17-11-7-5-10(12)6-8-11/h5-8H,3-4,9H2,1-2H3\\n\",\n        \"output\": \" 1.8365383433483438e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][C]\\n\",\n        \"output\": \" 4-Heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Bromotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Methyl-2-hexanol\\n\",\n        \"output\": \" CCCCC(C)(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Carbaryl\\n\",\n        \"output\": \" CNC(=O)Oc1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,2',3,4,4',5',6-PCB\\n\",\n        \"output\": \" InChI=1S/C12H3Cl7/c13-4-1-2-5(6(14)3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3\\n\",\n        \"output\": \" -0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][S][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.676\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Clonazepam\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][N][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p,p'-Biphenyldiamine \\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Diazinon\\n\",\n        \"output\": \" CCOP(=S)(OCC)Oc1cc(C)nc(n1)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Chrysene\\n\",\n        \"output\": \" 8.770008211436339e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Cyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3\\n\",\n        \"output\": \" 1-Phenylethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(C)Cl\\n\",\n        \"output\": \" 2-Chlorobutane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dulcin\\n\",\n        \"output\": \" [C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][Branch1][C][N][=O][C][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CNC(=O)ON=C(SC)C(=O)N(C)C\\n\",\n        \"output\": \" 0.106\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 17a-Methyltestosterone\\n\",\n        \"output\": \" [C][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 2,4-Dimethylpyridine\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C2Cl3F3/c3-1(4,6)2(5,7)8\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCCCCC1CCCC1\\n\",\n        \"output\": \" 8.317637711026709e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Phosalone\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Bromoethane\\n\",\n        \"output\": \" InChI=1S/C2H5Br/c1-2-3/h2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H18N2O3/c1-14(22)12-13-17-18(23)20(15-8-4-2-5-9-15)21(19(17)24)16-10-6-3-7-11-16/h2-11,17H,12-13H2,1H3\\n\",\n        \"output\": \" kebuzone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" phthalamide\\n\",\n        \"output\": \" c1cC2C(=O)NC(=O)C2cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(O)C(C)(C)C\\n\",\n        \"output\": \" 3,3-Dimethyl-2-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Cypermethrin\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,3-Dimethylpyridine\\n\",\n        \"output\": \" Cc1cccnc1C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][#C]\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ethyl acetate\\n\",\n        \"output\": \" InChI=1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" Indole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2-Propylene oxide\\n\",\n        \"output\": \" [C][C][C][O][Ring1][Ring1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Propanol\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 3-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Caproaldehyde\\n\",\n        \"output\": \" CCCCCC=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Buturon\\n\",\n        \"output\": \" 0.00012589254117941674 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Norethisterone\\n\",\n        \"output\": \" CC34CCC1C(CCC2=CC(=O)CCC12O)C3CCC4(O)C#C\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=N(=O)c1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 0.0004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)\\n\",\n        \"output\": \" Phenylthiourea\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Caffeine\\n\",\n        \"output\": \" Cn1cnc2n(C)c(=O)n(C)c(=O)c12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C17H12/c1-3-7-14-12(5-1)9-10-16-15-8-4-2-6-13(15)11-17(14)16/h1-10H,11H2\\n\",\n        \"output\": \" Benzo(a)fluorene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" C1C(O)CCC2(C)CC3CCC4(C)C5(C)CC6OCC(C)CC6OC5CC4C3C=C21\\n\",\n        \"output\": \" -7.32\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H10O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\",\n        \"output\": \" Ethyl benzoate \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2-Dinitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4N2O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][Ring1][C][C][C][=O]\\n\",\n        \"output\": \" 2-Ethylbutanal\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC34CCC1C(CCC2CC(O)CCC12C)C3CCC4=O\\n\",\n        \"output\": \" Epiandrosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-pyrrolidone\\n\",\n        \"output\": \" [O][=C][C][C][C][N][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CNC(=O)Oc1ccccc1C2OCCO2\\n\",\n        \"output\": \" 0.026915348039269153 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCO\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" methyl laurate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" thioanisole\\n\",\n        \"output\": \" c1ccccc1SC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1(C(C)(C)C)cc(C(C)(C)C)cc(OC(=O)NC)c1\\n\",\n        \"output\": \" butacarb\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" 0.00031622776601683794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Butylbenzene\\n\",\n        \"output\": \" 8.709635899560814e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,3-Dibromobenzene\\n\",\n        \"output\": \" [Br][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Fenfuram\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC(=O)c1ccc(O)cc1\\n\",\n        \"output\": \" Ethyl-p-hydroxybenzoate \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOP(=S)(OCC)ON=C(C#N)c1ccccc1\\n\",\n        \"output\": \" Phoxim\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.88\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 2-Methylanthracene\\n\",\n        \"output\": \" 1.0964781961431852e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 5-Methyl-5-ethylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC#C\\n\",\n        \"output\": \" 1-Butyne\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Acenapthylene\\n\",\n        \"output\": \" -3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl\\n\",\n        \"output\": \" Dieldrin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,3',4',5-PCB\\n\",\n        \"output\": \" InChI=1S/C12H6Cl4/c13-8-2-4-10(14)9(6-8)7-1-3-11(15)12(16)5-7/h1-6H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 2-Methylbutane\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" ethofumesate\\n\",\n        \"output\": \" CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCCSCC\\n\",\n        \"output\": \" 5.888436553555884e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Diphenylamine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cccc(C)c1NC(=O)c2cc(c(Cl)cc2O)S(N)(=O)=O\\n\",\n        \"output\": \" Xipamide\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Acenapthene\\n\",\n        \"output\": \" 2.344228815319923e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Bromo-2-methylpropane\\n\",\n        \"output\": \" CC(C)CBr\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCC=C(CC)C=O\\n\",\n        \"output\": \" 0.0034673685045253167 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-4-6(3)5-2/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Phenylthiourea\\n\",\n        \"output\": \" InChI=1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Phenylmethanol\\n\",\n        \"output\": \" [O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1,2,4-Trichlorobenzene\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3\\n\",\n        \"output\": \" p-t-Butylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COP(=S)(OC)Oc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" Ronnel\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-4-8-5-7(6)2/h3-5H,1-2H3\\n\",\n        \"output\": \" 3,4-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCc1ccc(C)cc1\\n\",\n        \"output\": \" -3.11\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/CHBrCl2/c2-1(3)4/h1H\\n\",\n        \"output\": \" Bromodichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Pyridazine\\n\",\n        \"output\": \" 12.589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlorzoxazone\\n\",\n        \"output\": \" Clc2ccc1oc(=O)[nH]c1c2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H13ClN6/c1-4-12-7-13-6(10)14-8(15-7)16-9(2,3)5-11/h4H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" Cyanazine\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCOC(=O)CCC\\n\",\n        \"output\": \" -1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Mebendazole\\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C20H16/c1-13-16-8-5-6-9-17(16)14(2)20-18(13)12-11-15-7-3-4-10-19(15)20/h3-12H,1-2H3\\n\",\n        \"output\": \" -7.02\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC12CC(=O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO\\n\",\n        \"output\": \" 0.0007762471166286919 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][O][C]\\n\",\n        \"output\": \" 0.10232929922807542 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3\\n\",\n        \"output\": \" 9,10-Dimethylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccc(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" 2,3,4-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Chloroanisole\\n\",\n        \"output\": \" InChI=1S/C7H7ClO/c1-9-7-5-3-2-4-6(7)8/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 1-Nitropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][Branch1][Ring1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][=O]\\n\",\n        \"output\": \" Flurochloridone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClC1(C2(Cl)C3(Cl)C4(Cl)C5(Cl)C1(Cl)C3(Cl)Cl)C5(Cl)C(Cl)(Cl)C24Cl\\n\",\n        \"output\": \" Mirex\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C24H38O4/c1-5-9-13-19(7-3)17-27-23(25)21-15-11-12-16-22(21)24(26)28-18-20(8-4)14-10-6-2/h11-12,15-16,19-20H,5-10,13-14,17-18H2,1-4H3\\n\",\n        \"output\": \" Di(2-ethylhexyl)-phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCS\\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][O][C]\\n\",\n        \"output\": \" Methyl propyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(=O)OC3(CCC4C2CCC1=CC(=O)CCC1C2CCC34C)C#C\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CON(C)C(=O)Nc1ccc(Br)c(Cl)c1\\n\",\n        \"output\": \" Chlorbromuron\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC(Cl)Cl\\n\",\n        \"output\": \" Trichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H6N2O2/c1-7-3-2-4(8)6-5(7)9/h2-3H,1H3,(H,6,8,9)\\n\",\n        \"output\": \" 0.15595525028269536 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][C][O][C][C]\\n\",\n        \"output\": \" 1,2-Diethoxyethane \\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methanol\\n\",\n        \"output\": \" InChI=1S/CH4O/c1-2/h2H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" allicin\\n\",\n        \"output\": \" [C][=C][C][S][=Branch1][C][=O][S][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cycloheptanol\\n\",\n        \"output\": \" InChI=1S/C7H14O/c8-7-5-3-1-2-4-6-7/h7-8H,1-6H2\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1cc(Cl)c(c(Cl)c1)c2c(Cl)cccc2Cl\\n\",\n        \"output\": \" 4.78630092322638e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Triclosan\\n\",\n        \"output\": \" -4.46\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C]\\n\",\n        \"output\": \" 3-Methyl-1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Pentylbenzene\\n\",\n        \"output\": \" CCCCCc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.0941124558508955e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" -3.955\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H\\n\",\n        \"output\": \" Napthacene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cortisone\\n\",\n        \"output\": \" CC12CC(=O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C]\\n\",\n        \"output\": \" Propane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cccc(n1)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" Nitrapyrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCC(C)(O)CC\\n\",\n        \"output\": \" -0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C(O)C(C)C\\n\",\n        \"output\": \" 2,4-Dimethyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" -3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" t-Butylbenzene \\n\",\n        \"output\": \" CC(C)(C)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2\\n\",\n        \"output\": \" -3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.012022644346174132 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCN(CC(C)=C)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" -6.124\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClCCBr\\n\",\n        \"output\": \" 1-Chloro-2-bromoethane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H11Cl/c1-4-5(2,3)6/h4H2,1-3H3\\n\",\n        \"output\": \" 2-Chloro-2-methylbutane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC1CO1\\n\",\n        \"output\": \" 0.2570395782768864 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCC(CC)COC(=O)c1ccccc1C(=O)OCC(CC)CCCC\\n\",\n        \"output\": \" -6.96\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Phenoxyethanol\\n\",\n        \"output\": \" [O][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Bromoiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccccc1N\\n\",\n        \"output\": \" 0.006165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Oc1ccc(Cl)cc1Cl\\n\",\n        \"output\": \" 0.028183829312644536 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cholanthrene\\n\",\n        \"output\": \" C1Cc2c3c1cccc3cc4c2ccc5ccccc54\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethanol\\n\",\n        \"output\": \" [C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3\\n\",\n        \"output\": \" -8.172\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)c2ccc(Cl)c(Cl)c2\\n\",\n        \"output\": \" 2,3',4',5-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Glyceryl triacetate\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" o-Nitrophenol\\n\",\n        \"output\": \" Oc1ccccc1N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,2-Dimethyl-1-butanol\\n\",\n        \"output\": \" CCC(C)(C)CO\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 2.1577444091526647e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1(OC)ccc(CC=C)cc1\\n\",\n        \"output\": \" Estragole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Octadecanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Br][Br]\\n\",\n        \"output\": \" Chlorodibromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1ccc(F)cc1\\n\",\n        \"output\": \" p-Fluoroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12/c1-3-5-6-4-2/h3H,1,4-6H2,2H3\\n\",\n        \"output\": \" 0.0005888436553555889 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCCCC(C)(O)CC\\n\",\n        \"output\": \" 0.025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C21H27FO6/c1-18-6-5-12(24)7-11(18)3-4-13-14-8-15(25)21(28,17(27)10-23)19(14,2)9-16(26)20(13,18)22/h5-7,13-16,23,25-26,28H,3-4,8-10H2,1-2H3\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Trifluralin\\n\",\n        \"output\": \" 2.0892961308540407e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Azodrin\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Piperine\\n\",\n        \"output\": \" 0.0003467368504525317 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C]\\n\",\n        \"output\": \" -1.228\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCN(CC)c1ccccc1\\n\",\n        \"output\": \" N,N-Diethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc2cnn(c1ccccc1)c(=O)c2Cl\\n\",\n        \"output\": \" Pyrazon\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Santonin\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=Branch1][N][=C][Ring1][Branch2][C][Ring1][N][O][C][Ring1][#C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2,3,6-Trichlorophenol\\n\",\n        \"output\": \" 0.0022908676527677724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1)c3ccc(OC(F)F)cc3\\n\",\n        \"output\": \" Flucythrinate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H24O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h3-11H2,1-2H3\\n\",\n        \"output\": \" -4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][C][C][Cl]\\n\",\n        \"output\": \" 1,3-Dichloropropane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3\\n\",\n        \"output\": \" -0.04\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Etofenprox\\n\",\n        \"output\": \" InChI=1S/C25H28O3/c1-4-27-22-15-13-21(14-16-22)25(2,3)19-26-18-20-9-8-12-24(17-20)28-23-10-6-5-7-11-23/h5-17H,4,18-19H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Di-n-propylsulfide\\n\",\n        \"output\": \" [C][C][C][S][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Sorbitol\\n\",\n        \"output\": \" OCC(O)C(O)C(O)C(O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Isopropyl formate\\n\",\n        \"output\": \" 0.2344228815319922 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H\\n\",\n        \"output\": \" 1,2-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Methyl-3-pentanol\\n\",\n        \"output\": \" CCC(C)(O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][I][C][=C][Branch1][Ring1][C][#N][C][=C][Ring1][=Branch2][I]\\n\",\n        \"output\": \" Ioxynil\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H20O/c1-3-4-5-6-7-8-9-10(2)11/h3-9H2,1-2H3\\n\",\n        \"output\": \" -3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Niridazole\\n\",\n        \"output\": \" [O][=C][N][C][C][N][Ring1][Branch1][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Clonazepam\\n\",\n        \"output\": \" InChI=1S/C15H10ClN3O3/c16-12-4-2-1-3-10(12)15-11-7-9(19(21)22)5-6-13(11)18-14(20)8-17-15/h1-7H,8H2,(H,18,20)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H3\\n\",\n        \"output\": \" 1.3803842646028839e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C21H20Cl2O3/c1-21(2)17(12-18(22)23)19(21)20(24)25-13-14-7-6-10-16(11-14)26-15-8-4-3-5-9-15/h3-12,17,19H,13H2,1-2H3\\n\",\n        \"output\": \" 5.116818355403073e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1c(NC(=O)OC(C)C(=O)NCC)cccc1\\n\",\n        \"output\": \" Carbetamide\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][I]\\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H15N2O3PS/c1-3-15-18(19,16-4-2)17-14-12(10-13)11-8-6-5-7-9-11/h5-9H,3-4H2,1-2H3\\n\",\n        \"output\": \" Phoxim\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanone\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" ampyrone\\n\",\n        \"output\": \" 0.23768402866248767 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Deoxycorticosterone\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/CH6N2/c1-3-2/h3H,2H2,1H3\\n\",\n        \"output\": \" Methyl hydrazine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 3-Heptanol \\n\",\n        \"output\": \" -1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Octene \\n\",\n        \"output\": \" -4.44\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.7585775750291838 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H7I/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" -4.55\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCO\\n\",\n        \"output\": \" 1-Propanol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Methyl-3-pentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Fc1cccc(F)c1C(=O)NC(=O)Nc2ccc(Cl)cc2\\n\",\n        \"output\": \" difluron\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1c(Cl)cccc1Cl\\n\",\n        \"output\": \" 2,6-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" C1SC(=S)NC1(=O)\\n\",\n        \"output\": \" 0.016982436524617443 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 0.0008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H14ClNO2/c1-12(2)8-16-14(11(12)15)7-9-5-3-4-6-10(9)13/h3-6H,7-8H2,1-2H3\\n\",\n        \"output\": \" 0.004591980128368685 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][Br]\\n\",\n        \"output\": \" Bromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.35\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOCCOCC\\n\",\n        \"output\": \" 1,2-Diethoxyethane \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Neburon\\n\",\n        \"output\": \" CCCCN(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4N2O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H\\n\",\n        \"output\": \" 0.0007943282347242813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3\\n\",\n        \"output\": \" 0.0005754399373371566 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Carvone\\n\",\n        \"output\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Chloroacetonitrile\\n\",\n        \"output\": \" ClCC#N\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCBr\\n\",\n        \"output\": \" -1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Nonanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Dibromobenzene\\n\",\n        \"output\": \" Brc1ccc(Br)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C13H22N2O/c1-15(2)13(16)14-12-7-8-6-11(12)10-5-3-4-9(8)10/h8-12H,3-7H2,1-2H3,(H,14,16)\\n\",\n        \"output\": \" -3.1710000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2-Diethoxyethane \\n\",\n        \"output\": \" [C][C][O][C][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" o-Nitrotoluene\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" 3-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-5-6-7(2,3)4/h5-6H2,1-4H3\\n\",\n        \"output\": \" 2,2-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methyl hydrazine\\n\",\n        \"output\": \" CNN\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Bromopropane\\n\",\n        \"output\": \" CCCBr\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(11)5(9)6(10)4(2)8/h1,11H\\n\",\n        \"output\": \" 2,3,4,5-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" o1c2ccccc2c3ccccc13\\n\",\n        \"output\": \" 2.5118864315095822e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3\\n\",\n        \"output\": \" Acetophenone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COP(=S)(OC)Oc1cc(Cl)c(Br)cc1Cl\\n\",\n        \"output\": \" Bromophos\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Ethyne\\n\",\n        \"output\": \" 1.9498445997580451 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-5(7)6(2,3)4/h1-4H3\\n\",\n        \"output\": \" 3,3-Dimethyl-2-butanone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" Nonane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1cccc(Br)c1\\n\",\n        \"output\": \" m-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1ccc(C)c2ccccc12\\n\",\n        \"output\": \" 7.244359600749906e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-5-6-7(8)9-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" Pentyl propanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H14/c1-9(2)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3\\n\",\n        \"output\": \" -4.12\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 3-Ethyl-3-pentanol\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" -6.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Methyl benzoate \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Benzo(a)fluorene\\n\",\n        \"output\": \" InChI=1S/C17H12/c1-3-7-14-12(5-1)9-10-16-15-8-4-2-6-13(15)11-17(14)16/h1-10H,11H2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-butenal\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3\\n\",\n        \"output\": \" -1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,1,2-Trichlorotrifluoroethane\\n\",\n        \"output\": \" [F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dicofol\\n\",\n        \"output\": \" InChI=1S/C14H9Cl5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Thiometon\\n\",\n        \"output\": \" InChI=1S/C6H15O2PS3/c1-4-11-5-6-12-9(10,7-2)8-3/h4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C22H27NO2/c1-4-22(24)10-8-18-16-6-5-15-11-19-14(13-23-25-19)12-20(15,2)17(16)7-9-21(18,22)3/h1,11,13,16-18,24H,5-10,12H2,2-3H3\\n\",\n        \"output\": \" -5.507000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -5.08\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Flumethasone\\n\",\n        \"output\": \" -5.6129999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" o-Chloroaniline\\n\",\n        \"output\": \" Nc1ccccc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H24N2O4/c1-2-3-6-15-19(25)28-16-24-20(26)22(23-21(24)27,17-11-7-4-8-12-17)18-13-9-5-10-14-18/h4-5,7-14H,2-3,6,15-16H2,1H3,(H,23,27)\\n\",\n        \"output\": \" 3-Hexanoyloxymethylphenyltoin\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H14N4OS/c1-8(2,3)5-6(13)12(9)7(14-4)11-10-5/h9H2,1-4H3\\n\",\n        \"output\": \" 0.005584701947368306 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17)\\n\",\n        \"output\": \" -2.322\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C3H3N/c1-2-3-4/h2H,1H2\\n\",\n        \"output\": \" Acrylonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" glucose\\n\",\n        \"output\": \" [O][C][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC=C)c1ccccc1\\n\",\n        \"output\": \" -2.369\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" phthalamide\\n\",\n        \"output\": \" -2.932\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2-Undecanol\\n\",\n        \"output\": \" -2.94\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Quinethazone\\n\",\n        \"output\": \" [C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][N][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][N][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3\\n\",\n        \"output\": \" 1-Heptene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccccc1n3c(C)nc2ccccc2c3=O\\n\",\n        \"output\": \" -2.925\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Quintozene\\n\",\n        \"output\": \" -5.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Ethyltoluene\\n\",\n        \"output\": \" 0.0006165950018614823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1cc(ccc1NS(=O)(=O)C(F)(F)F)S(=O)(=O)c2ccccc2\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Isobutyl acetate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][P][Ring1][#Branch2]\\n\",\n        \"output\": \" -6.68\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3\\n\",\n        \"output\": \" 1-Octene \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" Phenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" P,P'-DDE\\n\",\n        \"output\": \" 1.2589254117941662e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" salicylanilide\\n\",\n        \"output\": \" c1ccccc1NC(=O)c2c(O)cccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,1,2-Trichloroethane\\n\",\n        \"output\": \" InChI=1S/C2H3Cl3/c3-1-2(4)5/h2H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Fluoromethalone\\n\",\n        \"output\": \" CC1CC2C3CCC(O)(C(=O)C)C3(C)CC(O)C2(F)C4(C)C=CC(=O)C=C14\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" -0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCC(=O)OCC\\n\",\n        \"output\": \" 0.0018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C20H16/c1-13-16-8-5-6-9-17(16)14(2)20-18(13)12-11-15-7-3-4-10-19(15)20/h3-12H,1-2H3\\n\",\n        \"output\": \" 7,12-Dimethylbenz(a)anthracene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Griseofulvin\\n\",\n        \"output\": \" COC1=CC(=O)CC(C)C13Oc2c(Cl)c(OC)cc(OC)c2C3=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2-Methylheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)n2cncn2\\n\",\n        \"output\": \" Triadimefon\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Butanethiol \\n\",\n        \"output\": \" [C][C][C][C][S]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H10N2O3/c1-3-7(2)4(10)8-6(12)9-5(7)11/h3H2,1-2H3,(H2,8,9,10,11,12)\\n\",\n        \"output\": \" 0.0591561634175474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Sulfallate\\n\",\n        \"output\": \" CCN(CC)C(=S)SCC(Cl)=C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H17ClN2O4/c20-12-5-6-14-17(7-8-21-18(14)9-12)22-16-4-2-1-3-15(16)19(25)26-11-13(24)10-23/h1-9,13,23-24H,10-11H2,(H,21,22)\\n\",\n        \"output\": \" Glafenine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methanol\\n\",\n        \"output\": \" [C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C/C1CCC(\\\\C)CC1\\n\",\n        \"output\": \" trans-1,4-Dimethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2\\n\",\n        \"output\": \" -3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCN(=O)=O\\n\",\n        \"output\": \" Nitroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Anisole\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H12/c1-3-9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3\\n\",\n        \"output\": \" 4-Ethyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H10Cl2O2/c14-10-1-3-12(16)8(6-10)5-9-7-11(15)2-4-13(9)17/h1-4,6-7,16-17H,5H2\\n\",\n        \"output\": \" 0.00011142945335917292 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H20N2O/c1-17(2,14-10-6-4-7-11-14)18-16(20)19(3)15-12-8-5-9-13-15/h4-13H,1-3H3,(H,18,20)\\n\",\n        \"output\": \" Methyldymron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H\\n\",\n        \"output\": \" -1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,2-Diethylbenzene\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" O=N(=O)c1cc(Cl)c(Cl)cc1\\n\",\n        \"output\": \" 0.000630957344480193 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Hexadecane\\n\",\n        \"output\": \" InChI=1S/C16H34/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3-16H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2,3-Trichlorobenzene\\n\",\n        \"output\": \" Clc1cccc(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Reposal\\n\",\n        \"output\": \" 0.0020137242498623874 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cyclooctane\\n\",\n        \"output\": \" C1CCCCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Butyraldehyde\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" -5.88\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" Hexadecane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12NO4PS2/c1-7(5-8)6(9)4-14-12(13,10-2)11-3/h5H,4H2,1-3H3\\n\",\n        \"output\": \" Formothion\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pyrolan\\n\",\n        \"output\": \" InChI=1S/C13H15N3O2/c1-10-9-12(18-13(17)15(2)3)16(14-10)11-7-5-4-6-8-11/h4-9H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" DDT\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6HCl5O/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H\\n\",\n        \"output\": \" Pentachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC=CC=O\\n\",\n        \"output\": \" 2-butenal\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Trichloroacetonitrile\\n\",\n        \"output\": \" InChI=1S/C2Cl3N/c3-2(4,5)1-6\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=Branch1][C][=C][Cl]\\n\",\n        \"output\": \" 1,1-Dichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5,5-Diallylbarbital\\n\",\n        \"output\": \" InChI=1S/C10H12N2O3/c1-3-5-10(6-4-2)7(13)11-9(15)12-8(10)14/h3-4H,1-2,5-6H2,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" D-fenchone\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H12/c1-3-5-7-6-4-2/h1H,4-7H2,2H3\\n\",\n        \"output\": \" 1-Heptyne\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCCCCC(C)O\\n\",\n        \"output\": \" -2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccccc1O\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C]\\n\",\n        \"output\": \" -3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc2c(c1)ccc3c2ccc4c5ccccc5ccc43\\n\",\n        \"output\": \" 1.3489628825916533e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4BrCl/c7-5-1-3-6(8)4-2-5/h1-4H\\n\",\n        \"output\": \" p-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Oc1ccc(Cl)cc1C(=O)Nc2ccc(cc2Cl)N(=O)=O\\n\",\n        \"output\": \" 1.9952623149688786e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" glucose\\n\",\n        \"output\": \" OCC1OC(O)C(O)C(O)C1O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3\\n\",\n        \"output\": \" Eicosane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Flurochloridone\\n\",\n        \"output\": \" 8.974287945007491e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-5(2)6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" -3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H10N2O3/c1-3-4-8(2)5(11)9-7(13)10-6(8)12/h3H,1,4H2,2H3,(H2,9,10,11,12,13)\\n\",\n        \"output\": \" 5-Allyl-5-methylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2,4,5-Tetramethylbenzene\\n\",\n        \"output\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][=C][Ring1][Branch2][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H10O2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2\\n\",\n        \"output\": \" 2-Phenoxyethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H5NO/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)\\n\",\n        \"output\": \" 10.471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" -3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][N][C][=Branch1][C][=O][N][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][Ring1][=N]\\n\",\n        \"output\": \" -2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 4-Methyl-2-pentanone\\n\",\n        \"output\": \" -0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" p-Toluenesulfonamide \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Acetophenone\\n\",\n        \"output\": \" 0.05248074602497726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 7.585775750291836e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][Branch1][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][O][Ring1][P]\\n\",\n        \"output\": \" 0.0052360043658575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-2-4-5-3-1/h1-4H2\\n\",\n        \"output\": \" Tetrahydrofurane \\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Carvone\\n\",\n        \"output\": \" [C][C][=Branch1][C][=C][C][C][C][=C][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCCC=C\\n\",\n        \"output\": \" 3.63078054770101e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][C]\\n\",\n        \"output\": \" 2,3-Dimethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" Dibenzofurane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][=Branch2][C][=C][N][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 4.168693834703355e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Simetryn\\n\",\n        \"output\": \" [C][S][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][S][S][C][C]\\n\",\n        \"output\": \" Diethyldisulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,4-Dinitrobenzene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" ClCCl\\n\",\n        \"output\": \" -0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H7Cl/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" 0.0001174897554939529 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-t-Butylphenol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Niclosamide\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc2cc3cc4ccccc4cc3cc2c1\\n\",\n        \"output\": \" Napthacene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1(C)C(C=C(Br)Br)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" Deltamethrin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1cccc(C)c1C\\n\",\n        \"output\": \" 0.000630957344480193 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H6S/c1-2-3/h3H,2H2,1H3\\n\",\n        \"output\": \" Ethanethiol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Dinitramine\\n\",\n        \"output\": \" 3.3884415613920275e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" NS(=O)(=O)c1cc(ccc1Cl)C2(O)NC(=O)c3ccccc23\\n\",\n        \"output\": \" Chlorthalidone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][Branch1][C][O][C][Ring1][Branch2]\\n\",\n        \"output\": \" borneol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Pentanone\\n\",\n        \"output\": \" [C][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" C/C1CCC(\\\\C)CC1\\n\",\n        \"output\": \" 3.3884415613920276e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Methylphenanthrene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Vinclozolin\\n\",\n        \"output\": \" CC1(OC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2)C=C\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H5Cl/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" 0.004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C3H6/c1-3-2/h3H,1H2,2H3\\n\",\n        \"output\": \" 0.08317637711026708 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" COc1ccc(C=O)cc1\\n\",\n        \"output\": \" -1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Isobutylbenzene\\n\",\n        \"output\": \" InChI=1S/C10H14/c1-9(2)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CNC(=O)Oc1ccc(N(C)C)c(C)c1\\n\",\n        \"output\": \" 0.004365158322401661 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Nitrotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chlorzoxazone\\n\",\n        \"output\": \" InChI=1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C15H18O3/c1-8-10-4-6-15(3)7-5-11(16)9(2)12(15)13(10)18-14(8)17/h5,7-8,10,13H,4,6H2,1-3H3\\n\",\n        \"output\": \" 0.0008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Phenoxyethanol\\n\",\n        \"output\": \" OCCOc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Flucytosine\\n\",\n        \"output\": \" [N][C][=N][C][=Branch1][C][=O][NH1][C][=C][Ring1][#Branch1][F]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][=Branch2][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][C][Branch1][C][Cl][C][=Branch1][=N][=C][Branch1][C][Cl][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][Cl]\\n\",\n        \"output\": \" 5.272298614228232e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(C)C(=O)C\\n\",\n        \"output\": \" 0.2137962089502232 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1=C(C(=O)Nc2ccccc2)S(=O)(=O)CCO1\\n\",\n        \"output\": \" Oxycarboxin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6H\\n\",\n        \"output\": \" Lindane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C15H24NO4PS/c1-6-18-21(22,16-11(2)3)20-14-10-8-7-9-13(14)15(17)19-12(4)5/h7-12H,6H2,1-5H3,(H,16,22)\\n\",\n        \"output\": \" 6.397348354826482e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" p-Nitroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C][N][Branch2][Ring1][=C][S][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][=Ring1][#Branch1][Ring1][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Benfuracarb\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C17H20N4O6/c1-7-3-9-10(4-8(7)2)21(5-11(23)14(25)12(24)6-22)15-13(18-9)16(26)20-17(27)19-15/h3-4,11-12,14,22-25H,5-6H2,1-2H3,(H,20,26,27)\\n\",\n        \"output\": \" Riboflavin\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H6/c1-3-4-2/h3-4H,1-2H2\\n\",\n        \"output\": \" 0.013489628825916533 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1cccc2ccccc12\\n\",\n        \"output\": \" -3.7\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cycloheptene\\n\",\n        \"output\": \" [C][C][C][C][=C][C][C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Heptanone\\n\",\n        \"output\": \" InChI=1S/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCCCCC(=O)OC\\n\",\n        \"output\": \" 2.0417379446695274e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" N,N-Dimethylaniline\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Carbromal\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C16H13ClN2O/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\\n\",\n        \"output\": \" -3.7539999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Diallate\\n\",\n        \"output\": \" CC(C)N(C(C)C)C(=O)SCC(=CCl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Chlorobiphenyl\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Clc1ccccc1\\n\",\n        \"output\": \" Chlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\\n\",\n        \"output\": \" Chlorotoluron\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Propazine\\n\",\n        \"output\": \" [C][C][Branch1][C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C17H16Cl2O3/c1-11(2)22-16(20)17(21,12-6-8-14(18)9-7-12)13-4-3-5-15(19)10-13/h3-11,21H,1-2H3\\n\",\n        \"output\": \" -4.53\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(c(Cl)c1)n2nc(oc2=O)C(C)(C)C\\n\",\n        \"output\": \" -4.328\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Diphenyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-Heptanone\\n\",\n        \"output\": \" [C][C][C][C][=Branch1][C][=O][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-Bromonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1c(C)c(C)c(C)c(C)c1C\\n\",\n        \"output\": \" -5.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" m-Fluorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Nonanol\\n\",\n        \"output\": \" CCCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanol\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Bromophos\\n\",\n        \"output\": \" InChI=1S/C8H8BrCl2O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Hydrocortisone \\n\",\n        \"output\": \" -3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H5ClO/c7-5-2-1-3-6(8)4-5/h1-4,8H\\n\",\n        \"output\": \" 3-Chlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Hexadecanol\\n\",\n        \"output\": \" CCCCCCCCCCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Chlorothalonil\\n\",\n        \"output\": \" [C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nimetazepam\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" chlordimeform\\n\",\n        \"output\": \" InChI=1S/C10H13ClN2/c1-8-6-9(11)4-5-10(8)12-7-13(2)3/h4-7H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][=C][C][C][C][Branch1][C][O][Branch1][C][C][C][=C]\\n\",\n        \"output\": \" linalool\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=C1CCCCC1\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,3,4,6-Tetrachlorophenol\\n\",\n        \"output\": \" Oc1c(Cl)cc(Cl)c(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-4(2)3-5/h4-5H,3H2,1-2H3\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H16/c1-2-3-5-8-11-9-6-4-7-10-11/h4,6-7,9-10H,2-3,5,8H2,1H3\\n\",\n        \"output\": \" Pentylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H16Cl3NOS/c1-6(2)14(7(3)4)10(15)16-5-8(11)9(12)13/h6-7H,5H2,1-4H3\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2,4,5-Tetrachlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1ccc(O)cc1\\n\",\n        \"output\": \" p-Hydroxyacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Bromophos\\n\",\n        \"output\": \" 8.128305161640995e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H12ClF4N3O4/c1-2-22(8-10-11(17)4-3-5-12(10)18)15-13(23(25)26)6-9(16(19,20)21)7-14(15)24(27)28/h3-7H,2,8H2,1H3\\n\",\n        \"output\": \" Flumetralin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dimethyl phthalate\\n\",\n        \"output\": \" InChI=1S/C10H10O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-6H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC#N\\n\",\n        \"output\": \" Propionitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Heptachlor\\n\",\n        \"output\": \" -6.317\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][=C][O][P][=Branch1][C][=O][Branch1][=N][O][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" Tricresyl phosphate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Carbaryl\\n\",\n        \"output\": \" -3.2239999999999998\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Azintamide\\n\",\n        \"output\": \" -1.716\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.03\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,3,5-Tribromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3Br3/c7-4-1-5(8)3-6(9)2-4/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 5.623413251903491e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,3-Dimethylbutane\\n\",\n        \"output\": \" CC(C)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Naled\\n\",\n        \"output\": \" -2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1cc(Cl)c(c(Cl)c1)c2c(Cl)cccc2Cl\\n\",\n        \"output\": \" 2,2,4,6,6'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][Ring1][=C]\\n\",\n        \"output\": \" -7.87\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" cis-1,2-Dimethylcyclohexane\\n\",\n        \"output\": \" C/C1CCCCC1\\\\C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][I][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" m-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Benzo[ghi]perylene\\n\",\n        \"output\": \" 9.594006315159356e-10 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-4-5(2)3/h4-5H,1H2,2-3H3\\n\",\n        \"output\": \" 3-Methyl-1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cyclohexanone\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" CCC(C)CCO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" OC1C(O)C(O)C(O)C(O)C1O\\n\",\n        \"output\": \" 2.2387211385683394 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-5-7(8)9-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" 0.01778279410038923 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C22H24N2O4/c1-2-3-6-15-19(25)28-16-24-20(26)22(23-21(24)27,17-11-7-4-8-12-17)18-13-9-5-10-14-18/h4-5,7-14H,2-3,6,15-16H2,1H3,(H,23,27)\\n\",\n        \"output\": \" -5.886\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Riboflavin\\n\",\n        \"output\": \" Cc3cc2nc1c(=O)[nH]c(=O)nc1n(CC(O)C(O)C(O)CO)c2cc3C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Undecanol\\n\",\n        \"output\": \" CCCCCCCCCC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H20NO4PS/c1-6-11-16(17,13-5)15-9(4)7-10(12)14-8(2)3/h7-8H,6H2,1-5H3,(H,11,17)\\n\",\n        \"output\": \" 0.0003908408957924021 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" vamidothion\\n\",\n        \"output\": \" 13.931568029453036 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Iodofenphos\\n\",\n        \"output\": \" 2.39883291901949e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.19\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 17a-Methyltestosterone\\n\",\n        \"output\": \" CC1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3-\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-4(2)7-5(3)6/h4H,1-3H3\\n\",\n        \"output\": \" 0.28183829312644537 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][C][C][C][C]\\n\",\n        \"output\": \" Dihexyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" 1.202264434617413e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" ClC(Cl)CC(=O)NC2=C(Cl)C(=O)c1ccccc1C2=O\\n\",\n        \"output\": \" 9.332543007969906e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Branch2][Ring1][#C][C][O][C][=Branch1][C][=O][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][#Branch2][Branch1][C][C][C][C][Branch1][C][F][=C][Ring2][Ring1][=Branch2][F]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCC=C\\n\",\n        \"output\": \" 1-Octene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Quinoline\\n\",\n        \"output\": \" [C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=C1N(COC(=O)CCCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 2.9991625189876533e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h3-8H,1-2H3\\n\",\n        \"output\": \" 2,6-Dimethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Butan-2-ol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccc2c(c1)ccc3c4ccccc4ccc23\\n\",\n        \"output\": \" 8.770008211436339e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Hydroxyprogesterone-17a\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Anthracene\\n\",\n        \"output\": \" c1ccc2cc3ccccc3cc2c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)\\n\",\n        \"output\": \" Acetanilide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=c2[nH]c1CCCc1c(=O)n2C3CCCCC3\\n\",\n        \"output\": \" Lenacil\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,4-Dimethylphenol\\n\",\n        \"output\": \" Cc1ccc(O)c(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Cc1cccc(C)c1\\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3\\n\",\n        \"output\": \" Ethyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" p-terphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC=O\\n\",\n        \"output\": \" Propionaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Chloronapthalene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" m-Chloroiodobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4ClI/c7-5-2-1-3-6(8)4-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 4-Bromophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Nitronapthalene\\n\",\n        \"output\": \" O=N(=O)c1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Propylcyclopentane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Br][C][Branch1][C][Br][Br]\\n\",\n        \"output\": \" Tribromomethane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3,4-Dichloronitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Disulfiram\\n\",\n        \"output\": \" CCN(CC)C(=S)SSC(=S)N(CC)CC\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Ethyl-2-hexanal\\n\",\n        \"output\": \" [C][C][C][C][=C][Branch1][Ring1][C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H13NO4S/c1-9-11(18(15,16)8-7-17-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\\n\",\n        \"output\": \" 0.0052360043658575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" 3-Methylbutan-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O]\\n\",\n        \"output\": \" 9.549925860214369e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H5NO/c1-2-4-7-6(3-1)8-5-9-7/h1-5H\\n\",\n        \"output\": \" -1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)c2ccc(Cl)c(Cl)c2\\n\",\n        \"output\": \" -7.25\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-5-6(2,3)4/h5H2,1-4H3\\n\",\n        \"output\": \" 2,2-Dimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" OCCCC=C\\n\",\n        \"output\": \" 0.7079457843841379 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Etofenprox\\n\",\n        \"output\": \" CCOc1ccc(cc1)C(C)(C)COCc3cccc(Oc2ccccc2)c3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Diiodomethane\\n\",\n        \"output\": \" InChI=1S/CH2I2/c2-1-3/h1H2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Thymol\\n\",\n        \"output\": \" 0.006025595860743574 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][N][Branch1][Ring1][C][=O][C][=N][C][Branch1][C][Cl][=C][C][Branch1][Ring1][O][C][=N][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.6546055619755363e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Br]\\n\",\n        \"output\": \" 0.018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1cccc2c1Cc3ccccc32\\n\",\n        \"output\": \" -5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][Cl][C][Cl]\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Phenylethanol\\n\",\n        \"output\": \" InChI=1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Indan\\n\",\n        \"output\": \" InChI=1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)c1ccccc1\\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COC(=O)c1ccccc1C(=O)OC\\n\",\n        \"output\": \" Dimethyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" trans-1,4-Dimethylcyclohexane\\n\",\n        \"output\": \" InChI=1S/C8H16/c1-7-3-5-8(2)6-4-7/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" C1CCCCC1\\n\",\n        \"output\": \" -3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)Nc1nc(Cl)nc(NC(C)C)n1\\n\",\n        \"output\": \" Propazine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H15N3O2/c1-10-9-12(18-13(17)15(2)3)16(14-10)11-7-5-4-6-8-11/h4-9H,1-3H3\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Methylcholanthrene\\n\",\n        \"output\": \" c1cc(C)cc2c1c3cc4cccc5CCc(c45)c3cc2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][#C][C][C]\\n\",\n        \"output\": \" 3-Hexyne\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" -8.334\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3\\n\",\n        \"output\": \" 1-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Octanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1ccc2cc3ccccc3cc2c1\\n\",\n        \"output\": \" -6.96\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CC=C(C)C\\n\",\n        \"output\": \" -2.253\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" -0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" ampyrone\\n\",\n        \"output\": \" InChI=1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OCC(O)COC(=O)c1ccccc1Nc2ccnc3cc(Cl)ccc23\\n\",\n        \"output\": \" Glafenine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3\\n\",\n        \"output\": \" Triadimefon\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccnnc1\\n\",\n        \"output\": \" Pyridazine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Iodonapthalene\\n\",\n        \"output\": \" InChI=1S/C10H7I/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H12/c1-2-4-6-7-5-3-1/h1-2H,3-7H2\\n\",\n        \"output\": \" Cycloheptene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OCC(O)C(O)C(O)C(O)CO\\n\",\n        \"output\": \" Sorbitol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C15H10ClN3O3/c16-12-4-2-1-3-10(12)15-11-7-9(19(21)22)5-6-13(11)18-14(20)8-17-15/h1-7H,8H2,(H,18,20)\\n\",\n        \"output\": \" 0.00031695674630434934 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethyl octanoate\\n\",\n        \"output\": \" CCCCCCCC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCC(=C)C\\n\",\n        \"output\": \" -3.03\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C22H28F2O5/c1-11-6-13-14-8-16(23)15-7-12(26)4-5-19(15,2)21(14,24)17(27)9-20(13,3)22(11,29)18(28)10-25/h4-5,7,11,13-14,16-17,25,27,29H,6,8-10H2,1-3H3\\n\",\n        \"output\": \" Flumethasone\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Propyl acetate\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Propylbenzene \\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 4-Methyl-2-pentanol\\n\",\n        \"output\": \" CC(C)CC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Difenoxuron\\n\",\n        \"output\": \" -4.16\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N]\\n\",\n        \"output\": \" Isoproturon\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Benfuracarb\\n\",\n        \"output\": \" CCOC(=O)CCN(SN(C)C(=O)Oc1cccc2CC(C)(C)Oc21)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-6(2)3-4-8-5-7/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccccc1SC\\n\",\n        \"output\": \" thioanisole\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C]\\n\",\n        \"output\": \" -2.5180000000000002\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCCO\\n\",\n        \"output\": \" 0.057543993733715694 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" NC(=O)c1ccccc1\\n\",\n        \"output\": \" 0.1096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,2,4-Trichlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H7NO2/c1-2-3-4(5)6/h2-3H2,1H3\\n\",\n        \"output\": \" 1-Nitropropane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Octene \\n\",\n        \"output\": \" InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][S][C][=N][N][=C][Branch1][=Branch2][C][=Branch1][C][=O][N][Ring1][#Branch1][N][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Metribuzin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Hexamethylbenzene\\n\",\n        \"output\": \" Cc1c(C)c(C)c(C)c(C)c1C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H11NO2/c1-13-12(14)15-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3,(H,13,14)\\n\",\n        \"output\": \" 0.0005970352865838372 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethofumesate\\n\",\n        \"output\": \" [C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H13NO2/c1-2-7-13-10(12)8-3-5-9(11)6-4-8/h3-6H,2,7,11H2,1H3\\n\",\n        \"output\": \" Risocaine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2-Dichlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,3-Dibromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4Br2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3\\n\",\n        \"output\": \" Ethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Ethyl butyrate\\n\",\n        \"output\": \" 0.05248074602497726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCl\\n\",\n        \"output\": \" 1-Chlorohexane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-5-7-6(2)3/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" Propylisopropylether\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C]\\n\",\n        \"output\": \" Hexane \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Linuron\\n\",\n        \"output\": \" CON(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H15Cl/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\",\n        \"output\": \" 1-Chloroheptane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Estrone\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Ethyl decanoate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Dimethyl phthalate\\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Furane\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][C][C][C][Branch1][Branch1][C][Ring1][Branch1][Cl][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl]\\n\",\n        \"output\": \" 1.380384264602884e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Nc1nc(=O)[nH]cc1F\\n\",\n        \"output\": \" -0.972\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCN(CC)C(=O)C(=CCOP(=O)(OC)OC)Cl\\n\",\n        \"output\": \" 3.3342641276323497 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H8ClNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\",\n        \"output\": \" p-Chloroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H7Br2Cl2O4P/c1-10-13(9,11-2)12-3(5)4(6,7)8/h3H,1-2H3\\n\",\n        \"output\": \" 0.005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3,5-Dimethylpyridine\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-3-7(2)5-8-4-6/h3-5H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4-Chlorotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Cyclohexene\\n\",\n        \"output\": \" -2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C17H19NO3/c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15/h2-3,6-9,12H,1,4-5,10-11,13H2\\n\",\n        \"output\": \" 0.0003467368504525317 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1ccccn1\\n\",\n        \"output\": \" 2-Hydroxypyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3,5-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" dibutyl sebacate\\n\",\n        \"output\": \" 0.00012705741052085407 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Branch1][C][O][Branch1][=Branch1][C][=Branch1][C][=O][C][C][Ring1][=Branch2][Branch1][C][C][C][C][Branch1][C][O][C][Ring1][#C][Branch1][C][F][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2]\\n\",\n        \"output\": \" Fluoromethalone\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Linuron\\n\",\n        \"output\": \" InChI=1S/C9H10Cl2N2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-hydroxypyridine\\n\",\n        \"output\": \" [O][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Chlorotoluene\\n\",\n        \"output\": \" Cc1ccccc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" chlordimeform\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Methylpentane\\n\",\n        \"output\": \" CCC(C)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Diethyl ether \\n\",\n        \"output\": \" InChI=1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Propane\\n\",\n        \"output\": \" -1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClC1=C(Cl)C(Cl)(C(=C1Cl)Cl)C2(Cl)C(=C(Cl)C(=C2Cl)Cl)Cl\\n\",\n        \"output\": \" Dienochlor\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/CH4/h1H4\\n\",\n        \"output\": \" Methane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H\\n\",\n        \"output\": \" Furfural\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 2-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H20N2O/c1-11-7-5-6-10-13(11)16-14(17)15-12-8-3-2-4-9-12/h2-4,8-9,11,13H,5-7,10H2,1H3,(H2,15,16,17)\\n\",\n        \"output\": \" Siduron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 6-Methylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" Cyclooctanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Nitronapthalene\\n\",\n        \"output\": \" InChI=1S/C10H7NO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][F]\\n\",\n        \"output\": \" 0.00042657951880159257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" COc2ccc(Oc1ccc(NC(=O)N(C)C)cc1)cc2\\n\",\n        \"output\": \" -4.16\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H10INO/c14-12-9-5-4-8-11(12)13(16)15-10-6-2-1-3-7-10/h1-9H,(H,15,16)\\n\",\n        \"output\": \" 6.165950018614822e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C14H9ClF2N2O2/c15-8-4-6-9(7-5-8)18-14(21)19-13(20)12-10(16)2-1-3-11(12)17/h1-7H,(H2,18,19,20,21)\\n\",\n        \"output\": \" 9.549925860214369e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Monuron\\n\",\n        \"output\": \" 0.0012882495516931337 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Cypermethrin\\n\",\n        \"output\": \" InChI=1S/C22H19Cl2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C\\n\",\n        \"output\": \" -5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCN(CC)C(=O)SCCC\\n\",\n        \"output\": \" Pebulate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" -1.661\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethane\\n\",\n        \"output\": \" CC\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p,p'-Biphenyldiamine \\n\",\n        \"output\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C19H14/c1-13-12-15-7-3-4-8-16(15)18-11-10-14-6-2-5-9-17(14)19(13)18/h2-12H,1H3\\n\",\n        \"output\": \" 2.570395782768865e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-4-8-5-7(6)2/h3-5H,1-2H3\\n\",\n        \"output\": \" 2.290867652767773 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Ethylnaphthalene \\n\",\n        \"output\": \" -4.17\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Ethyl heptanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3\\n\",\n        \"output\": \" D-fenchone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Anthraquinone\\n\",\n        \"output\": \" [O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H16ClN5/c1-5(2)11-8-13-7(10)14-9(15-8)12-6(3)4/h5-6H,1-4H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" NS(=O)(=O)c3cc2c(NC(Cc1ccccc1)NS2(=O)=O)cc3C(F)(F)F\\n\",\n        \"output\": \" Bendroflumethiazide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Erythritol\\n\",\n        \"output\": \" OCC(O)C(O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" c1ccccc1n2ncc(N)c(Br)c2(=O)\\n\",\n        \"output\": \" 0.0007464487584100669 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Norea\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][C][C][C][C][Ring1][Branch2][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(=O)C3(C)CCC4C2C=C(C)C1=CC(=O)CCC1(C)C2CCC34C\\n\",\n        \"output\": \" 5.370317963702533e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Rovral\\n\",\n        \"output\": \" InChI=1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,3,4-Trimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Estrone\\n\",\n        \"output\": \" CC12CCC3C(CCc4cc(O)ccc34)C2CCC1=O\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methyl t-butyl ether \\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-5(2,3)6-4/h1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 9,10-Dimethylanthracene\\n\",\n        \"output\": \" Cc1c2ccccc2c(C)c3ccccc13\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" o-Chloroiodobenzene\\n\",\n        \"output\": \" Clc1ccccc1I\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Ethyl-1-hexanol\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][#N]\\n\",\n        \"output\": \" Phthalonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl-p-hydroxybenzoate \\n\",\n        \"output\": \" InChI=1S/C9H10O3/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Triphenylene\\n\",\n        \"output\": \" InChI=1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Pentadiene \\n\",\n        \"output\": \" C=CCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCC(=O)CCCC\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O]\\n\",\n        \"output\": \" 0.05128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Methoprene\\n\",\n        \"output\": \" COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Thiometon\\n\",\n        \"output\": \" [C][C][S][C][C][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" p-Bromoacetanilide\\n\",\n        \"output\": \" -3.083\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1(C)CON(Cc2ccccc2Cl)C1=O\\n\",\n        \"output\": \" Clomazone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][P][C][=Branch1][C][=O][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][Cl][C][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring1][N][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" Kepone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CNC(=O)Oc1ccccc1C(C)C\\n\",\n        \"output\": \" -2.863\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H8Cl3NO3/c14-8(15)5-9(18)17-11-10(16)12(19)6-3-1-2-4-7(6)13(11)20/h1-4,8H,5H2,(H,17,18)\\n\",\n        \"output\": \" -5.03\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 4-hydroxypyridine\\n\",\n        \"output\": \" 10.471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3\\n\",\n        \"output\": \" 0.05248074602497726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" -0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benzene \\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C11H24O/c1-3-4-5-6-7-8-9-10-11(2)12/h11-12H,3-10H2,1-2H3\\n\",\n        \"output\": \" -2.94\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Chloroaniline\\n\",\n        \"output\": \" InChI=1S/C6H6ClN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Tetrahydropyran \\n\",\n        \"output\": \" InChI=1S/C5H10O/c1-2-4-6-5-3-1/h1-5H2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" m-Chlorobromobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Diphenylmethane\\n\",\n        \"output\": \" 8.317637711026709e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Phthalonitrile\\n\",\n        \"output\": \" InChI=1S/C8H4N2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Methyl-1,3-Butadiene \\n\",\n        \"output\": \" InChI=1S/C5H8/c1-4-5(2)3/h4H,1-2H2,3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Chloroethylene\\n\",\n        \"output\": \" -1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C11H16/c1-7-6-8(2)10(4)11(5)9(7)3/h6H,1-5H3\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCC(=O)OC\\n\",\n        \"output\": \" Methyl octanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,3,4-Trichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H3Cl3O/c7-3-1-2-4(10)6(9)5(3)8/h1-2,10H\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Napthylamine\\n\",\n        \"output\": \" [N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Methylcyclohexene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Oc1ccc(C=O)cc1\\n\",\n        \"output\": \" 0.1096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C26H22ClF3N2O3/c1-16(2)24(32-22-12-11-18(14-21(22)27)26(28,29)30)25(33)35-23(15-31)17-7-6-10-20(13-17)34-19-8-4-3-5-9-19/h3-14,16,23-24,32H,1-2H3\\n\",\n        \"output\": \" -8.003\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 1,1-Dichloroethane\\n\",\n        \"output\": \" 0.05128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][O][C][=O]\\n\",\n        \"output\": \" Butyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)Nc1ccc(F)cc1\\n\",\n        \"output\": \" 0.016595869074375606 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)CC\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClCC(Cl)Cl\\n\",\n        \"output\": \" 1,1,2-Trichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-t-Butylphenol\\n\",\n        \"output\": \" CC(C)(C)c1ccc(O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-methylpteridine\\n\",\n        \"output\": \" Cc2ncc1nccnc1n2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1c(C)c(C)c(C)c(C)c1C\\n\",\n        \"output\": \" Hexamethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,4-Difluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C15H19ClN4O3/c1-15(2,3)12-18-20(14(22)23-12)11-7-6-9(8-10(11)16)17-13(21)19(4)5/h6-8H,1-5H3,(H,17,21)\\n\",\n        \"output\": \" -4.328\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-9(2)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3\\n\",\n        \"output\": \" Isobutylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C)C\\n\",\n        \"output\": \" 0.018113400926196024 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Diethyl ether \\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][S][C][=C][C][=C][Branch1][C][Cl][N][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" Azintamide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dapsone\\n\",\n        \"output\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-7-3-5-8(2)6-4-7/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" trans-1,4-Dimethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3\\n\",\n        \"output\": \" 1-Propanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1(OC)ccc(CC=C)cc1\\n\",\n        \"output\": \" 0.001202264434617413 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" O=C1NC(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 7.998342550070293e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=O)C(C)(C)C\\n\",\n        \"output\": \" 3,3-Dimethyl-2-butanone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCOC(=O)c1cncn1C(C)c2ccccc2\\n\",\n        \"output\": \" 1.8407720014689545e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Napthylamine\\n\",\n        \"output\": \" InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Hexestrol\\n\",\n        \"output\": \" [C][C][C][Branch1][P][C][Branch1][Ring1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-3-4-5-6(7)8-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" Propyl propanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COc1ccc(C=CC)cc1\\n\",\n        \"output\": \" Anethole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Chloroethane\\n\",\n        \"output\": \" [Cl][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methyl-2-pentanol\\n\",\n        \"output\": \" 0.32359365692962827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Metronidazole\\n\",\n        \"output\": \" InChI=1S/C6H9N3O3/c1-5-7-4-6(9(11)12)8(5)2-3-10/h4,10H,2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" c1cC2C(=O)NC(=O)C2cc1\\n\",\n        \"output\": \" 0.001169499391019871 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=N][N][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" -4.09\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Carbofuran\\n\",\n        \"output\": \" InChI=1S/C12H15NO3/c1-12(2)7-8-5-4-6-9(10(8)16-12)15-11(14)13-3/h4-6H,7H2,1-3H3,(H,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Methylheptane\\n\",\n        \"output\": \" InChI=1S/C8H18/c1-4-6-7-8(3)5-2/h8H,4-7H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3\\n\",\n        \"output\": \" -3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" benzoin\\n\",\n        \"output\": \" OC(C(=O)c1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][Br]\\n\",\n        \"output\": \" 1-Bromopentane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" -5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Propanol\\n\",\n        \"output\": \" [C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCC1CCCC1\\n\",\n        \"output\": \" -4.74\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Acridine\\n\",\n        \"output\": \" -3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=Branch1][=N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.0012882495516931337 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" gentisin\\n\",\n        \"output\": \" [C][=C][Branch1][C][O][C][C][=Branch1][C][=O][C][C][=C][Branch1][C][O][C][=C][C][Ring1][#Branch1][O][C][Ring1][N][C][=C][Ring1][P][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][C][=C]\\n\",\n        \"output\": \" 0.008375292821268827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its oil solubility in room temperature. ->\",\n        \"input\": \" p-Nitrophenol\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -4.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC#N\\n\",\n        \"output\": \" 1.8197008586099834 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" p-Hydroxybenzaldehyde \\n\",\n        \"output\": \" 0.1096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.884031503126606 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CNC(=O)C(C)SCCSP(=O)(OC)(OC)\\n\",\n        \"output\": \" 1.1440000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#C]\\n\",\n        \"output\": \" -6.59\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-7-3-5-8(2)6-4-7/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" -4.47\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H13ClN2O2/c1-13(2)10(14)12-7-4-5-9(15-3)8(11)6-7/h4-6H,1-3H3,(H,12,14)\\n\",\n        \"output\": \" -2.5639999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Nitrapyrin\\n\",\n        \"output\": \" 0.00017378008287493763 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Isopropyl formate\\n\",\n        \"output\": \" InChI=1S/C4H8O2/c1-4(2)6-3-5/h3-4H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 0.33884415613920255 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H3I2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H\\n\",\n        \"output\": \" -3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Chlordane\\n\",\n        \"output\": \" InChI=1S/C10H6Cl8/c11-3-1-2-4(5(3)12)9(16)7(14)6(13)8(2,15)10(9,17)18/h2-5H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Nitromethane\\n\",\n        \"output\": \" 1.8197008586099834 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Cortisone\\n\",\n        \"output\": \" 0.0007762471166286919 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc2cc3ccccc3cc2c1\\n\",\n        \"output\": \" Anthracene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-2-4(10)6(9)5(3)8/h1-2,10H\\n\",\n        \"output\": \" 0.0021379620895022326 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3\\n\",\n        \"output\": \" 2-Methylbutan-2-ol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H9Cl/c1-4(2)3-5/h4H,3H2,1-2H3\\n\",\n        \"output\": \" 1-Chloro-2-methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H5N/c1-2-4-6-5-3-1/h1-5H\\n\",\n        \"output\": \" Pyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H\\n\",\n        \"output\": \" -3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-isoPrbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(C(C)C)CC=C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3\\n\",\n        \"output\": \" -1.28\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Dichloromethane\\n\",\n        \"output\": \" [Cl][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H9Cl4O4P/c1-16-19(15,17-2)18-10(5-11)6-3-8(13)9(14)4-7(6)12/h3-5H,1-2H3\\n\",\n        \"output\": \" 3.006076302628229e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Oc2ncc1nccnc1n2\\n\",\n        \"output\": \" -1.9469999999999998\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H10BrClN2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\",\n        \"output\": \" Chlorbromuron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,4-Dichlorobenzene\\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H14F3NO/c1-23-11-16(13-6-3-2-4-7-13)18(24)17(12-23)14-8-5-9-15(10-14)19(20,21)22/h2-12H,1H3\\n\",\n        \"output\": \" Fluridone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Reposal\\n\",\n        \"output\": \" CCC1(C(=O)NC(=O)NC1=O)C2=CCC3CCC2C3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H12/c1-10-5-4-8-13-12-7-3-2-6-11(12)9-14(10)13/h2-8H,9H2,1H3\\n\",\n        \"output\": \" 1-Methylfluorene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)Cc1ccccc1\\n\",\n        \"output\": \" Isobutylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Azobenzene\\n\",\n        \"output\": \" 3.5481338923357534e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1)c3ccc(OC(F)F)cc3\\n\",\n        \"output\": \" -6.876\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pentobarbital\\n\",\n        \"output\": \" InChI=1S/C11H18N2O3/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Nitrofen\\n\",\n        \"output\": \" InChI=1S/C12H7Cl2NO3/c13-8-1-6-12(11(14)7-8)18-10-4-2-9(3-5-10)15(16)17/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" -3.082\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0812830516164099 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" Methylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][O][C]\\n\",\n        \"output\": \" Dimethoxymethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][O][Ring1][#Branch2]\\n\",\n        \"output\": \" 1,8-Cineole\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Benzo(b)fluorene\\n\",\n        \"output\": \" 9.120108393559115e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.23988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethion\\n\",\n        \"output\": \" CCOP(=S)(OCC)SCSP(=S)(OCC)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" c1cccc2c3c(C)cc4ccccc4c3ccc12\\n\",\n        \"output\": \" -6.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][N][C][=N][C][N][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=N][=Ring1][#Branch2]\\n\",\n        \"output\": \" -0.8759999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Deoxycorticosterone\\n\",\n        \"output\": \" 0.0003548133892335753 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.2589254117941662e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=N(=O)c1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" 0.005128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H7ClO/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3\\n\",\n        \"output\": \" 3-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)CO\\n\",\n        \"output\": \" 2-Methylpropan-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)C(C)C)N(=O)=O\\n\",\n        \"output\": \" 3.235936569296281e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H8Cl2N2O4/c14-7-1-4-12(18)9(5-7)13(19)16-11-3-2-8(17(20)21)6-10(11)15/h1-6,18H,(H,16,19)\\n\",\n        \"output\": \" Niclosamide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)\\n\",\n        \"output\": \" Methocarbamol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H8S/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" thioanisole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC12CC(=O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO\\n\",\n        \"output\": \" Cortisone\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Phenylethanol\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cc(Cl)c(Cl)c(Cl)c1\\n\",\n        \"output\": \" 1,2,3,5-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][C][Ring1][#C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzo(j)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Decalin\\n\",\n        \"output\": \" 6.456542290346549e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)N(C(C)C)C(=O)SCC(=CCl)Cl\\n\",\n        \"output\": \" Diallate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" BrCBr\\n\",\n        \"output\": \" Dibromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Trietazine\\n\",\n        \"output\": \" -4.06\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nonane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Estrone\\n\",\n        \"output\": \" -3.955\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Methyl-3-pentanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 2,2-Dimethylpentane\\n\",\n        \"output\": \" -4.36\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Chloropicrin\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-7-10(2)12-6-4-3-5-11(12)8-9/h3-8H,1-2H3\\n\",\n        \"output\": \" 1,3-Dimethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" N#Cc1ccccc1C#N\\n\",\n        \"output\": \" -2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H\\n\",\n        \"output\": \" 1,4-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Methylheptane\\n\",\n        \"output\": \" 6.9183097091893625e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Oc1ccc(Cl)cc1\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=O]\\n\",\n        \"output\": \" 0.2344228815319922 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" m-Chloroiodobenzene\\n\",\n        \"output\": \" -3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" rhodanine\\n\",\n        \"output\": \" InChI=1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2-Dichlorotetrafluoroethane\\n\",\n        \"output\": \" [F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O]\\n\",\n        \"output\": \" 37.15352290971726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" -3.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H5Br/c1-2-3/h2H2,1H3\\n\",\n        \"output\": \" Bromoethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" COC(=O)C\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H15NO2/c1-2-3-8-14-11(13)9-4-6-10(12)7-5-9/h4-7H,2-3,8,12H2,1H3\\n\",\n        \"output\": \" Butamben\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.616\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCN(CC(C)=C)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" Ethalfluralin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\\n\",\n        \"output\": \" P,P'-DDE\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)CBr\\n\",\n        \"output\": \" 0.003715352290971724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-6-9-15-13(10-11)8-7-12-4-2-3-5-14(12)15/h2-10H,1H3\\n\",\n        \"output\": \" 2-Methylphenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 3-Methyl-2-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" cis-2-Pentene\\n\",\n        \"output\": \" -2.54\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cyfluthrin\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][Branch1][C][F][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CN(C)C=Nc1ccc(Cl)cc1C\\n\",\n        \"output\": \" 0.0013803842646028853 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" c1nccc(C(=O)NN)c1\\n\",\n        \"output\": \" 1.02093948370768 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCCSCCC\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Flucythrinate\\n\",\n        \"output\": \" InChI=1S/C26H23F2NO4/c1-17(2)24(18-11-13-21(14-12-18)32-26(27)28)25(30)33-23(16-29)19-7-6-10-22(15-19)31-20-8-4-3-5-9-20/h3-15,17,23-24,26H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" -1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][=C][C][C][C][Branch1][C][O][Branch1][C][C][C][=C]\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][C][#N]\\n\",\n        \"output\": \" Chloroacetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Carboxin\\n\",\n        \"output\": \" [C][C][=C][Branch1][#Branch1][S][C][C][O][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C=CCS(=O)SCC=C\\n\",\n        \"output\": \" allicin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Dieldrin\\n\",\n        \"output\": \" InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-5(2)3-4-6/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 3-Methylbutan-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCc1ccccc1CC\\n\",\n        \"output\": \" 1,2-Diethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-3-5-7(8)6-4-2/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 0.039810717055349734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CNC(=O)Oc1ccccc1OC(C)C\\n\",\n        \"output\": \" -2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H16F3N3O4/c1-3-5-6-17(4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" -5.53\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzophenone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Acetonitrile\\n\",\n        \"output\": \" [C][C][#N]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Flurochloridone\\n\",\n        \"output\": \" InChI=1S/C12H10Cl2F3NO/c13-5-7-6-18(11(19)10(7)14)9-3-1-2-8(4-9)12(15,16)17/h1-4,7,10H,5-6H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][O][C][Branch2][Ring1][C][C][O][C][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring1][O]\\n\",\n        \"output\": \" Monotropitoside\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][=C][C][#N]\\n\",\n        \"output\": \" 1.4125375446227544 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-7,11H,1-3H3\\n\",\n        \"output\": \" Thymol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2,3-Trimethylbenzene \\n\",\n        \"output\": \" Cc1cccc(C)c1C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3\\n\",\n        \"output\": \" Estradiol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-5-6-7(2,3)8/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" 0.08317637711026708 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethyl heptanoate\\n\",\n        \"output\": \" CCCCCCC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3\\n\",\n        \"output\": \" -4.69\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccnc(C)c1\\n\",\n        \"output\": \" 2,4-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dimethyldisulfide\\n\",\n        \"output\": \" [C][S][S][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Primidone\\n\",\n        \"output\": \" [C][C][C][Branch1][N][C][=Branch1][C][=O][N][C][N][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Butyne\\n\",\n        \"output\": \" CCC#C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Chrysene\\n\",\n        \"output\": \" c1ccc2c(c1)ccc3c4ccccc4ccc23\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Hexachloro-1,3-butadiene\\n\",\n        \"output\": \" InChI=1S/C4Cl6/c5-1(3(7)8)2(6)4(9)10\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Ic1cccc2ccccc12\\n\",\n        \"output\": \" -4.55\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Naled\\n\",\n        \"output\": \" COP(=O)(OC)OC(Br)C(Cl)(Cl)Br\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility of given compound in room temperature? ->\",\n        \"input\": \" 2,3,4-Trichlorophenol\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-Aminophenol\\n\",\n        \"output\": \" [N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.07943282347242814 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O6/c7-1-3-4(9)5(10)6(11,2-8)12-3/h3-5,7-11H,1-2H2\\n\",\n        \"output\": \" 4.36515832240166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6HCl5/c7-2-1-3(8)5(10)6(11)4(2)9/h1H\\n\",\n        \"output\": \" Pentachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-Methylnapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1cc2cccc3c4cccc5cccc(c(c1)c23)c54\\n\",\n        \"output\": \" 1.5703628043335515e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Toluene \\n\",\n        \"output\": \" InChI=1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCC=C\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Methoproptryne\\n\",\n        \"output\": \" 0.0011803206356517297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,3-Dichloronitrobenzene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Hexylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][Branch1][C][C][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Diazinon\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][Branch1][N][C][=Branch1][C][=O][N][C][N][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0022908676527677724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1cc(cc(N(=O)=O)c1O)N(=O)=O\\n\",\n        \"output\": \" 0.03499451670283573 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Bendroflumethiazide\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Terbutryn\\n\",\n        \"output\": \" [C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccc(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" 2.691534803926914e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2-Phenoxyethanol\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-5-3-2-4-6-5/h5H,2-4H2,1H3\\n\",\n        \"output\": \" 1.288249551693134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H20/c1-2-3-4-7-10-8-5-6-9-10/h10H,2-9H2,1H3\\n\",\n        \"output\": \" -6.08\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Oxadiazon\\n\",\n        \"output\": \" InChI=1S/C15H18Cl2N2O3/c1-8(2)21-12-7-11(9(16)6-10(12)17)19-14(20)22-13(18-19)15(3,4)5/h6-8H,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Carbophenthion\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][O][C][=N][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" -1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 7-methylpteridine\\n\",\n        \"output\": \" Cc2cnc1cncnc1n2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Azobenzene\\n\",\n        \"output\": \" N(=Nc1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 1.8197008586099827e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Flutriafol\\n\",\n        \"output\": \" OC(Cn1cncn1)(c2ccc(F)cc2)c3ccccc3F\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,2-Dichloroethane\\n\",\n        \"output\": \" ClCCCl\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCCCCCCCCC(C)O\\n\",\n        \"output\": \" 0.0011481536214968829 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Ioxynil\\n\",\n        \"output\": \" -3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCO\\n\",\n        \"output\": \" -7.0\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3\\n\",\n        \"output\": \" -3.03\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methylpropan-1-ol\\n\",\n        \"output\": \" CC(C)CO\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=Branch1][N][=C][Ring1][Branch2][C][Ring1][N][O][C][Ring1][#C][=O][C]\\n\",\n        \"output\": \" Santonin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Chlorimuron-ethyl (ph 7)\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][N][Branch1][Ring1][C][=O][C][=N][C][Branch1][C][Cl][=C][C][Branch1][Ring1][O][C][=N][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-Heptanol\\n\",\n        \"output\": \" CCCC(O)CCC\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7-\\n\",\n        \"output\": \" 0.0034673685045253167 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Isopropyltoluene\\n\",\n        \"output\": \" 0.00017378008287493763 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][Ring1][C][C][C][O]\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)C)CC=C(C)C\\n\",\n        \"output\": \" -2.593\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Formetanate\\n\",\n        \"output\": \" CNC(=O)Oc1cccc(N=CN(C)C)c1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylpropane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C)CC\\n\",\n        \"output\": \" 0.0591561634175474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1O\\n\",\n        \"output\": \" 9.549925860214369e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" vamidothion\\n\",\n        \"output\": \" InChI=1S/C8H18NO4PS2/c1-7(8(10)9-2)15-5-6-16-14(11,12-3)13-4/h7H,5-6H2,1-4H3,(H,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Glyceryl triacetate\\n\",\n        \"output\": \" InChI=1S/C9H14O6/c1-6(10)13-4-9(15-8(3)12)5-14-7(2)11/h9H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Fluoromethalone\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][Branch1][C][O][Branch1][=Branch1][C][=Branch1][C][=O][C][C][Ring1][=Branch2][Branch1][C][C][C][C][Branch1][C][O][C][Ring1][#C][Branch1][C][F][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Chlorazine\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Cyclohexene\\n\",\n        \"output\": \" [C][C][C][C][=C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Hexyne\\n\",\n        \"output\": \" CCC#CCC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Decanone\\n\",\n        \"output\": \" InChI=1S/C10H20O/c1-3-4-5-6-7-8-9-10(2)11/h3-9H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1CO1\\n\",\n        \"output\": \" 1,2-Propylene oxide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H12O4/c1-12-7-4-3-6-5-14-10(11)8(6)9(7)13-2/h3-4,6,8H,5H2,1-2H3\\n\",\n        \"output\": \" meconin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(Cl)Cl\\n\",\n        \"output\": \" 1,1-Dichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H18N4O3/c1-3-4-9-15-13(19)18-11-8-6-5-7-10(11)16-12(18)17-14(20)21-2/h5-8H,3-4,9H2,1-2H3,(H,15,19)(H,16,17,20)\\n\",\n        \"output\": \" Benomyl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pteridine\\n\",\n        \"output\": \" c2cnc1ncncc1n2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3\\n\",\n        \"output\": \" borneol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C]\\n\",\n        \"output\": \" Mecarbam\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Thiourea\\n\",\n        \"output\": \" InChI=1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Isobutylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOc1ccc(NC(=O)C)cc1\\n\",\n        \"output\": \" Phenacetin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H9Cl4O4P/c1-16-19(15,17-2)18-10(5-11)6-3-8(13)9(14)4-7(6)12/h3-5H,1-2H3\\n\",\n        \"output\": \" Stirofos\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][O][C][=Branch1][C][=O][C][Branch1][C][Cl][=C][Branch1][C][C][C][Ring1][=Branch2][=C][Ring1][=N]\\n\",\n        \"output\": \" 4.149540426343624e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,3-Dinitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4N2O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H18N4O3/c1-3-4-9-15-13(19)18-11-8-6-5-7-10(11)16-12(18)17-14(20)21-2/h5-8H,3-4,9H2,1-2H3,(H,15,19)(H,16,17,20)\\n\",\n        \"output\": \" -4.883\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2Cl3N/c3-2(4,5)1-6\\n\",\n        \"output\": \" -2.168\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)Nc1cc(NS(=O)(=O)C(F)(F)F)c(C)cc1C\\n\",\n        \"output\": \" -3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C25H28O3/c1-4-27-22-15-13-21(14-16-22)25(2,3)19-26-18-20-9-8-12-24(17-20)28-23-10-6-5-7-11-23/h5-17H,4,18-19H2,1-3H3\\n\",\n        \"output\": \" -8.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" garage\\n\",\n        \"output\": \" garage does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3,3-Dimethylpentane\\n\",\n        \"output\": \" InChI=1S/C7H16/c1-5-7(3,4)6-2/h5-6H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3\\n\",\n        \"output\": \" 0.008317637711026709 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][O][C][Branch1][C][C][C][S][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 6.309573444801929e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=Cc1ccco1\\n\",\n        \"output\": \" Furfural\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 2,3,5,6-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" Fluorene \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H4BrCl/c3-1-2-4/h1-2H2\\n\",\n        \"output\": \" 1-Chloro-2-bromoethane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\",\n        \"output\": \" Atrazine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#C][Ring1][#Branch2]\\n\",\n        \"output\": \" Chrysene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" COC(=O)Nc2nc1ccc(cc1[nH]2)C(=O)c3ccccc3\\n\",\n        \"output\": \" -3.88\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][O][C][Branch1][C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][Branch1][C][C][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -5.19\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H3N/c1-2-3/h1H3\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3\\n\",\n        \"output\": \" d-Limonene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ronnel\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methyl-1-Butene\\n\",\n        \"output\": \" [C][C][C][=Branch1][C][=C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][Branch2][O][C][=Branch1][C][=O][N][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" butacarb\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Tetrahydrofurane \\n\",\n        \"output\": \" 3.0902954325135905 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Monuron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" o-Xylene \\n\",\n        \"output\": \" Cc1ccccc1C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,3-Dichloronitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3Cl2NO2/c7-4-2-1-3-5(6(4)8)9(10)11/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethanol\\n\",\n        \"output\": \" CCO\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility expressed as a logarithm in mol/L of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H9Cl2NO3/c1-3-12(2)10(16)15(11(17)18-12)9-5-7(13)4-8(14)6-9/h3-6H,1H2,2H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3\\n\",\n        \"output\": \" p-Methoxybenzaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC=C\\n\",\n        \"output\": \" Chloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Nitramine\\n\",\n        \"output\": \" CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Octene \\n\",\n        \"output\": \" [C][C][C][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H14ClN5/c1-4-10-7-12-6(9)13-8(14-7)11-5(2)3/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" Atrazine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC(=O)N(C)C(=O)CSP(=S)(OCC)OCC\\n\",\n        \"output\": \" Mecarbam\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1c(cccc1N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" 2,6-Dinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Amitraz\\n\",\n        \"output\": \" CN(C=Nc1ccc(C)cc1C)C=Nc2ccc(C)cc2C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" Acridine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C14H12/c1-10-5-4-8-13-12-7-3-2-6-11(12)9-14(10)13/h2-8H,9H2,1H3\\n\",\n        \"output\": \" -5.22\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Isobutylbenzene\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2\\n\",\n        \"output\": \" Eriodictyol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C18H16N2O4/c1-13(21)24-12-20-16(22)18(19-17(20)23,14-8-4-2-5-9-14)15-10-6-3-7-11-15/h2-11H,12H2,1H3,(H,19,23)\\n\",\n        \"output\": \" -4.47\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][C][=C][C][=Branch1][C][=O][NH1][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 0.15595525028269536 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" p-Bromoiodobenzene\\n\",\n        \"output\": \" -4.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCC/C=C/C\\n\",\n        \"output\": \" 0.00015135612484362088 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2,4-Trimethylbenzene\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Iodoethane\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl\\n\",\n        \"output\": \" Triallate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1c2ccccc2cc3ccccc13\\n\",\n        \"output\": \" 9-Methylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.00047863009232263854 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" DNOC\\n\",\n        \"output\": \" [C][C][=C][C][=Branch1][=C][=C][C][Branch1][=Branch1][N][=Branch1][C][=O][=O][=C][Ring1][=Branch2][O][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Decanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethofumesate\\n\",\n        \"output\": \" CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Ethion\\n\",\n        \"output\": \" -5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C][C][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Glyceryl triacetate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1(OC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2)C=C\\n\",\n        \"output\": \" Vinclozolin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,2,5-Trimethylhexane\\n\",\n        \"output\": \" CC(C)CCC(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" meconin\\n\",\n        \"output\": \" c1c(OC)c(OC)C2C(=O)OCC2c1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Chlorimuron-ethyl (ph 7)\\n\",\n        \"output\": \" 2.6546055619755363e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)S(N)(=O)=O)N(=O)=O\\n\",\n        \"output\": \" oryzalin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H4Cl2/c1-2(3)4/h2H,1H3\\n\",\n        \"output\": \" 1,1-Dichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H\\n\",\n        \"output\": \" -3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H6Cl4/c13-8-2-4-10(14)9(6-8)7-1-3-11(15)12(16)5-7/h1-6H\\n\",\n        \"output\": \" 2,3',4',5-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\\n\",\n        \"output\": \" -4.16\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" Hexane \\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methyl hydrazine\\n\",\n        \"output\": \" [C][N][N]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H14N2O3/c1-4-5-10(6(2)3)7(13)11-9(15)12-8(10)14/h4,6H,1,5H2,2-3H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 0.01958844673505989 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Hexanone\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Propionaldehyde\\n\",\n        \"output\": \" [C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3,4-Dichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H4Cl2O/c7-5-2-1-4(9)3-6(5)8/h1-3,9H\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][#C]\\n\",\n        \"output\": \" -4.24\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H8BrN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\\n\",\n        \"output\": \" -3.127\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzo(k)fluoranthene\\n\",\n        \"output\": \" c1ccc2cc3c4cccc5cccc(c3cc2c1)c45\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3\\n\",\n        \"output\": \" -5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" booklet\\n\",\n        \"output\": \" booklet does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2,2,5-Trimethylhexane\\n\",\n        \"output\": \" -5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H9Cl5/c15-11-5-1-9(2-6-11)13(14(17,18)19)10-3-7-12(16)8-4-10/h1-8,13H\\n\",\n        \"output\": \" DDT\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Epitostanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][C][C][S][C][Ring1][Ring1][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Metolcarb\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][N][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C3H7Br/c1-2-3-4/h2-3H2,1H3\\n\",\n        \"output\": \" -1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCO\\n\",\n        \"output\": \" 1-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H14O6/c1-6(10)13-4-9(15-8(3)12)5-14-7(2)11/h9H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.251188643150958 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Methyl-1-Butene\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][Ring1][C][#C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Buturon\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" 0.0006456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,2-Dimethylpentane\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc1ccccc1Cl\\n\",\n        \"output\": \" 2-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,3,5-Trichlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3Cl3/c7-4-1-5(8)3-6(9)2-4/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" isocarbamid\\n\",\n        \"output\": \" [C][N][Branch1][N][C][=Branch1][C][=O][N][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4N2O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H\\n\",\n        \"output\": \" 1,2-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H7Cl/c8-6-7-4-2-1-3-5-7/h1-5H,6H2\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCc1ccccc1\\n\",\n        \"output\": \" 0.00042657951880159257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][Branch1][C][F][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][N][Ring1][#Branch1][C][C][Ring2][Ring1][C][C][C][Branch1][C][O][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Triamcinolone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H4N4/c1-2-9-6-5(8-1)3-7-4-10-6/h1-4H\\n\",\n        \"output\": \" Pteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" p-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methyl acrylate\\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1c(Cl)cccc1c2ccccc2\\n\",\n        \"output\": \" 3-Chlorobiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H12/c1-3-13-7-9-15-11-12-16-10-8-14-4-2-6-18-17(5-1)19(13)21(15)22(16)20(14)18/h1-12H\\n\",\n        \"output\": \" Benzo[ghi]perylene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO\\n\",\n        \"output\": \" Deoxycorticosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC#CCC\\n\",\n        \"output\": \" 3-Hexyne\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dienestrol\\n\",\n        \"output\": \" CC=C(C(=CC)c1ccc(O)cc1)c2ccc(O)cc2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C21H30O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h11,15-18,22H,3-10,12H2,1-2H3\\n\",\n        \"output\": \" Deoxycorticosterone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Pyrolan\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Acetophenone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H16N2O2/c1-3-18-14(17)13-9-15-10-16(13)11(2)12-7-5-4-6-8-12/h4-11H,3H2,1-2H3\\n\",\n        \"output\": \" 1.8407720014689545e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccnnc1\\n\",\n        \"output\": \" 12.589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Dapsone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2-Dinitrobenzene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Isazofos\\n\",\n        \"output\": \" CCOP(=S)(OCC)Oc1nc(Cl)n(n1)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3\\n\",\n        \"output\": \" 17a-Methyltestosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3\\n\",\n        \"output\": \" 0.0008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][=C]\\n\",\n        \"output\": \" 0.2570395782768864 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.698243652461746e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Coumachlor\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][C][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Brc1cc(Br)cc(Br)c1\\n\",\n        \"output\": \" 1,3,5-Tribromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Quinethazone\\n\",\n        \"output\": \" InChI=1S/C10H12ClN3O3S/c1-2-9-13-7-4-6(11)8(18(12,16)17)3-5(7)10(15)14-9/h3-4,9,13H,2H2,1H3,(H,14,15)(H2,12,16,17)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\",\n        \"output\": \" Ethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Chlorothalonil\\n\",\n        \"output\": \" c1(C#N)c(Cl)c(C#N)c(Cl)c(Cl)c(Cl)1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)(C)CCO\\n\",\n        \"output\": \" 0.31622776601683794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Benzocaine\\n\",\n        \"output\": \" -2.616\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Nc1cccc2ccccc12\\n\",\n        \"output\": \" 0.012022644346174132 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(N(=O)=O)c(C)c1\\n\",\n        \"output\": \" Fenitrothion\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Heptanol \\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9H\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-2-3-4-5-6-7-8/h8H,2-7H2,1H3\\n\",\n        \"output\": \" -1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Carbophenthion\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" DEF\\n\",\n        \"output\": \" [C][C][C][C][S][P][=Branch1][C][=O][Branch1][=Branch1][S][C][C][C][C][S][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Mebendazole\\n\",\n        \"output\": \" -3.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2,4-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,3-Dimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1c2ccccc2c3ccccc13\\n\",\n        \"output\": \" Fluorene \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccc2ccccc2c1\\n\",\n        \"output\": \" -3.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2.754228703338169e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methy-2-Butene\\n\",\n        \"output\": \" CC=C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Etofenprox\\n\",\n        \"output\": \" 2.511886431509582e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-5(2)4-6(3)7/h5H,4H2,1-3H3\\n\",\n        \"output\": \" -0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Betamethasone-17-valerate\\n\",\n        \"output\": \" [C][C][C][C][C][=Branch1][C][=O][O][C][Branch2][Ring2][O][C][Branch1][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][=Branch1][Ring2][Ring1][C][C][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" Trietazine\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Malonic acid diethylester\\n\",\n        \"output\": \" InChI=1S/C7H12O4/c1-3-10-6(8)5-7(9)11-4-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Decene\\n\",\n        \"output\": \" 3.090295432513592e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Clonazepam\\n\",\n        \"output\": \" -3.4989999999999997\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-Chloroacetanilide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCC(CC)C=O\\n\",\n        \"output\": \" 0.007413102413009177 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 2,4-Dimethyl-2-pentanol \\n\",\n        \"output\": \" 0.12022644346174127 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 5-Nonanone\\n\",\n        \"output\": \" [C][C][C][C][C][=Branch1][C][=O][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H13NO4/c1-12-11(13)16-9-5-3-2-4-8(9)10-14-6-7-15-10/h2-5,10H,6-7H2,1H3,(H,12,13)\\n\",\n        \"output\": \" 0.026915348039269153 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H14O/c1-5(2)7(8)6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" 2,4-Dimethyl-3-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 4-Pentene-1-ol\\n\",\n        \"output\": \" InChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=C][C][Ring1][Branch1][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" Cholanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 1,2,3-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" 0.001995262314968879 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-5-6(2,3)7/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" 2-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Oc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 0.18197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" o-Chloroiodobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4ClI/c7-5-3-1-2-4-6(5)8/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCC(=O)OC\\n\",\n        \"output\": \" Methyl decanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC1=CCCCC1\\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 2-Ethyl-1-butanol\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC12CC(O)C3C(CCC4=CC(=O)C=CC34C)C2CCC1(O)C(=O)CO\\n\",\n        \"output\": \" Prednisolone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Pentamethylbenzene\\n\",\n        \"output\": \" Cc1cc(C)c(C)c(C)c1C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1cccc(C)c1\\n\",\n        \"output\": \" m-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(Sc2ccc(OP(=S)(OC)OC)cc2)cc1\\n\",\n        \"output\": \" 5.794286964268809e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-5(7)6(2,3)4/h5,7H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cc(=O)[nH]c(=S)[nH]1\\n\",\n        \"output\": \" methylthiouracil\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Octyne \\n\",\n        \"output\": \" CCCCCCC#C\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C11H10ClNO2/c1-3-8(2)15-11(14)13-10-6-4-5-9(12)7-10/h1,4-8H,2H3,(H,13,14)\\n\",\n        \"output\": \" -2.617\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" -2.86\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1c(cc(cc1N(=O)=O)N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" -3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ICI\\n\",\n        \"output\": \" Diiodomethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Pentanoyloxymethylphenytoin\\n\",\n        \"output\": \" O=C1N(COC(=O)CCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" N-Methylaniline \\n\",\n        \"output\": \" [C][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,3,4,5-Tetrachlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(11)5(9)6(10)4(2)8/h1,11H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Butane\\n\",\n        \"output\": \" [C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Testosterone\\n\",\n        \"output\": \" InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][O][C][=Ring1][Branch1]\\n\",\n        \"output\": \" Furane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1c(Cl)c(Cl)c(N(=O)=O)c(Cl)c1Cl\\n\",\n        \"output\": \" Quintozene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2,3-Trichlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCC(=O)OCC\\n\",\n        \"output\": \" -2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C24H28N2O4/c1-2-3-4-5-12-17-21(27)30-18-26-22(28)24(25-23(26)29,19-13-8-6-9-14-19)20-15-10-7-11-16-20/h6-11,13-16H,2-5,12,17-18H2,1H3,(H,25,29)\\n\",\n        \"output\": \" 3-Octanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" ClC(=C)Cl\\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1cc(Cl)c(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" 2,3,4,5-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Caproaldehyde\\n\",\n        \"output\": \" [C][C][C][C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H16N2O3/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its solubility. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COP(=S)(OC)SCC(=O)N(C(C)C)c1ccc(Cl)cc1\\n\",\n        \"output\": \" Anilofos\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Fructose\\n\",\n        \"output\": \" InChI=1S/C6H12O6/c7-1-3-4(9)5(10)6(11,2-8)12-3/h3-5,7-11H,1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" NS(=O)(=O)c3cc2c(NC(Cc1ccccc1)NS2(=O)=O)cc3C(F)(F)F\\n\",\n        \"output\": \" -3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1-Chlorobutane\\n\",\n        \"output\": \" -2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Phenacetin\\n\",\n        \"output\": \" CCOc1ccc(NC(=O)C)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H6N2O4/c1-5-6(8(10)11)3-2-4-7(5)9(12)13/h2-4H,1H3\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" exchange\\n\",\n        \"output\": \" exchange does not have compound\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Methylcyclohexene \\n\",\n        \"output\": \" CC1=CCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cyanazine\\n\",\n        \"output\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][O][N][C][Branch1][C][C][Branch1][C][C][C][#N][=N][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Octanol\\n\",\n        \"output\": \" InChI=1S/C8H18O/c1-3-5-6-7-8(9)4-2/h8-9H,3-7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Methyl acetate\\n\",\n        \"output\": \" 2.884031503126606 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H18N2O/c1-9(2)10-5-7-11(8-6-10)13-12(15)14(3)4/h5-9H,1-4H3,(H,13,15)\\n\",\n        \"output\": \" -3.536\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(O)CC\\n\",\n        \"output\": \" 3-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3\\n\",\n        \"output\": \" 1-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2-Methy-2-Butene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Propylbenzene \\n\",\n        \"output\": \" [C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 3-Methyl-2-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Methoxybenzaldehyde\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethyl benzoate \\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Aminocarb\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][=Branch1][N][Branch1][C][C][C][C][Branch1][C][C][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\\n\",\n        \"output\": \" 1.2589254117941662e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-4(2)5(3)6/h4-6H,1-3H3\\n\",\n        \"output\": \" 0.660693448007596 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H16ClO2PS3/c1-3-13-15(16,14-4-2)18-9-17-11-7-5-10(12)6-8-11/h5-8H,3-4,9H2,1-2H3\\n\",\n        \"output\": \" Carbophenthion\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1,4-Dimethylnaphthalene \\n\",\n        \"output\": \" -4.14\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCOC(=O)CC\\n\",\n        \"output\": \" Ethyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H18O2/c1-3-4-5-6-7-8-9(10)11-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" 0.0006760829753919819 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 0.033884415613920256 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][C][=O]\\n\",\n        \"output\": \" 0.09772372209558107 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Clc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" 1,2,4-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][O]\\n\",\n        \"output\": \" 0.00776247116628692 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CSCS(=O)CC(CO)NC(=O)C=Cc1c(C)[nH]c(=O)[nH]c1=O\\n\",\n        \"output\": \" Sparsomycin (3,8mg/ml)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" borneol\\n\",\n        \"output\": \" CC1(C)C2CCC1(C)C(O)C2\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2,3-Trimethylbenzene \\n\",\n        \"output\": \" InChI=1S/C9H12/c1-7-5-4-6-8(2)9(7)3/h4-6H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4BrF/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" o-Fluorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1ccccn1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H18/c1-2-3-4-6-9-12-10-7-5-8-11-12/h5,7-8,10-11H,2-4,6,9H2,1H3\\n\",\n        \"output\": \" -5.21\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" FC(F)(F)c1cccc(c1)N2CC(CCl)C(Cl)C2=O\\n\",\n        \"output\": \" Flurochloridone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-12H2,1H3\\n\",\n        \"output\": \" 1-Dodecanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" ClC(Cl)C(Cl)Cl\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Branch1][N][C][Ring1][O][=C][C][Ring1][#C][=C][Ring2][Ring1][Ring1][=C][Ring1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Benzo(k)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4N2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H\\n\",\n        \"output\": \" 0.0004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2Cl6/c3-1(4,5)2(6,7)8\\n\",\n        \"output\": \" Hexachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COP(=O)(OC)OC(Br)C(Cl)(Cl)Br\\n\",\n        \"output\": \" Naled\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-hexylresorcinol\\n\",\n        \"output\": \" InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Pentamethylbenzene\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][S][S][C]\\n\",\n        \"output\": \" Dimethyldisulfide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H\\n\",\n        \"output\": \" Fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H12/c1-3-5-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" -3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Ethyl nonanoate\\n\",\n        \"output\": \" -3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][O][P][=Branch1][C][=S][Branch1][Branch1][O][C][C][C][S][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2-Decanone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Methyl pentanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" N,N-Dimethylacetamide\\n\",\n        \"output\": \" InChI=1S/C4H9NO/c1-4(6)5(2)3/h1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Chloroethane\\n\",\n        \"output\": \" InChI=1S/C2H5Cl/c1-2-3/h2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Ethyl decanoate\\n\",\n        \"output\": \" -4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC1CCCCC1NC(=O)Nc2ccccc2\\n\",\n        \"output\": \" 7.762471166286911e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Brc1ccccc1Br\\n\",\n        \"output\": \" 1,2-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyclopentane \\n\",\n        \"output\": \" InChI=1S/C5H10/c1-2-4-5-3-1/h1-5H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Ethyl pyridine\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Pentyl propanoate\\n\",\n        \"output\": \" [C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSC(C)(C)C\\n\",\n        \"output\": \" -4.755\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Bromoiodobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4BrI/c7-5-1-3-6(8)4-2-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Benzo(j)fluoranthene\\n\",\n        \"output\": \" 1e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Bibenzyl \\n\",\n        \"output\": \" C(Cc1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" p-Methylaniline \\n\",\n        \"output\": \" -1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][N]\\n\",\n        \"output\": \" Cyclopentyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][O][N][C][Branch1][C][C][Branch1][C][C][C][#N][=N][Ring1][=N]\\n\",\n        \"output\": \" -3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" gentisin\\n\",\n        \"output\": \" 0.0011402497875611685 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" C1CCOC1\\n\",\n        \"output\": \" 3.0902954325135905 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Malonic acid diethylester\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H13N3O2/c1-9-7-11(15-17-9)12(16)14-13-8-10-5-3-2-4-6-10/h2-7,13H,8H2,1H3,(H,14,16)\\n\",\n        \"output\": \" 0.0034593937782612205 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Br][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Bromodichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H8N2/c7-8-6-4-2-1-3-5-6/h1-5,8H,7H2\\n\",\n        \"output\": \" 0.07\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethyl propyl ether\\n\",\n        \"output\": \" CCCOCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Fc1ccc(F)cc1\\n\",\n        \"output\": \" -1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Indole\\n\",\n        \"output\": \" InChI=1S/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9H\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2-Methylnapthalene\\n\",\n        \"output\": \" -3.77\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Methylnapthalene\\n\",\n        \"output\": \" Cc1ccc2ccccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCC(=O)OCC\\n\",\n        \"output\": \" Ethyl octanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCc1ccccc1\\n\",\n        \"output\": \" Propylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Barban\\n\",\n        \"output\": \" InChI=1S/C11H9Cl2NO2/c12-6-1-2-7-16-11(15)14-10-5-3-4-9(13)8-10/h3-5,8H,6-7H2,(H,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCc1ccc(C)cc1\\n\",\n        \"output\": \" 4-Ethyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1,3-Butadiene\\n\",\n        \"output\": \" -1.87\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Chloro-2-methylbutane\\n\",\n        \"output\": \" CCC(C)(C)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" N(=Nc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Azobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring1][C][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 1.7701089583174183e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Thiophene\\n\",\n        \"output\": \" [C][C][=C][S][C][=Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Metronidazole\\n\",\n        \"output\": \" [C][C][=N][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][N][Ring1][Branch2][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 17a-Methyltestosterone\\n\",\n        \"output\": \" InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Sulfallate\\n\",\n        \"output\": \" -3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Pentanol\\n\",\n        \"output\": \" CCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Cresol\\n\",\n        \"output\": \" InChI=1S/C7H8O/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=O]\\n\",\n        \"output\": \" -1.995\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,3,6-Trichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H3Cl3O/c7-3-1-2-4(8)6(10)5(3)9/h1-2,10H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dihexyl phthalate\\n\",\n        \"output\": \" CCCCCCOC(=O)c1ccccc1C(=O)OCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0007943282347242813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][Branch1][C][O][=C][C][Branch1][C][O][=C][C][=C][Ring1][Branch2][C][C][C][C][C][C]\\n\",\n        \"output\": \" -2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Acrolein\\n\",\n        \"output\": \" C=CC=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" NC(=S)Nc1ccccc1\\n\",\n        \"output\": \" Phenylthiourea\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][O]\\n\",\n        \"output\": \" Estradiol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyclohexene\\n\",\n        \"output\": \" InChI=1S/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1c(C)c2c3ccccc3ccc2c4ccccc14\\n\",\n        \"output\": \" -7.01\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethyl butyrate\\n\",\n        \"output\": \" [C][C][C][C][C][O][C][=Branch1][C][=O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring1][=Branch1][Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 2,2',3,3'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methylanthracene\\n\",\n        \"output\": \" Cc1ccc2cc3ccccc3cc2c1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Medrogestone\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][C][Branch1][C][C][C][C][C][C][C][=C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][C][C][C][Ring2][Ring1][Branch1][Ring1][P][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Stirofos\\n\",\n        \"output\": \" COP(=O)(OC)OC(=CCl)c1cc(Cl)c(Cl)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Nonyne \\n\",\n        \"output\": \" 5.7543993733715664e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)C=Nc1ccc(Cl)cc1C\\n\",\n        \"output\": \" chlordimeform\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Carbazole\\n\",\n        \"output\": \" InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCC(=O)OCC\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COc1ccc(C=O)cc1\\n\",\n        \"output\": \" p-Methoxybenzaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-6(2)4-3-5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 0.07244359600749903 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Amitraz\\n\",\n        \"output\": \" [C][N][Branch1][#C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Fc1ccccc1Br\\n\",\n        \"output\": \" o-Fluorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0005970352865838372 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H13NO2/c1-7-4-8(2)6-9(5-7)13-10(12)11-3/h4-6H,1-3H3,(H,11,12)\\n\",\n        \"output\": \" XMC\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Methylphenanthrene\\n\",\n        \"output\": \" Cc1ccc2c(ccc3ccccc32)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" NC(=S)N\\n\",\n        \"output\": \" Thiourea\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Chlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Tetradecane\\n\",\n        \"output\": \" InChI=1S/C14H30/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3-14H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Chloropicrin\\n\",\n        \"output\": \" ClC(Cl)(Cl)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3\\n\",\n        \"output\": \" linalool\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Iodopropane\\n\",\n        \"output\": \" InChI=1S/C3H7I/c1-2-3-4/h2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Bendroflumethiazide\\n\",\n        \"output\": \" NS(=O)(=O)c3cc2c(NC(Cc1ccccc1)NS2(=O)=O)cc3C(F)(F)F\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC\\n\",\n        \"output\": \" 0.00042657951880159257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][Branch1][=N][O][Ring1][Branch1][C][=Branch1][C][=O][N][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.461\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCN(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" 1.698243652461746e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 9,10-Dimethylanthracene\\n\",\n        \"output\": \" -6.57\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" flight\\n\",\n        \"output\": \" flight does not have SELFIES\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Chloroheptane\\n\",\n        \"output\": \" InChI=1S/C7H15Cl/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C3H3N/c1-2-3-4/h2H,1H2\\n\",\n        \"output\": \" 1.4125375446227544 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H7NO2/c1-3(2)4(5)6/h3H,1-2H3\\n\",\n        \"output\": \" 2-Nitropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Methyl-2-pentanone\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H19ClF3NO3/c1-22(2)17(12-19(24)23(25,26)27)20(22)21(29)31-18(13-28)14-7-6-10-16(11-14)30-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\",\n        \"output\": \" Cyhalothrin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-hydroxypyridine\\n\",\n        \"output\": \" Oc1ccncc1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" hook\\n\",\n        \"output\": \" hook does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=N(=O)c1ccccc1N(=O)=O\\n\",\n        \"output\": \" 0.0007943282347242813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(O)CCC\\n\",\n        \"output\": \" 4-Heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ronnel\\n\",\n        \"output\": \" InChI=1S/C8H8Cl3O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cyclohexanol \\n\",\n        \"output\": \" [O][C][C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H8/c1-3-2/h3H2,1-2H3\\n\",\n        \"output\": \" Propane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" NC(=O)c1cnccn1\\n\",\n        \"output\": \" 0.21527817347243727 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cc(C)c(C)cc1C\\n\",\n        \"output\": \" 1,2,4,5-Tetramethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCC=O\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3\\n\",\n        \"output\": \" -1.22\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Cl]\\n\",\n        \"output\": \" 1-Chloroheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Cycloheptene\\n\",\n        \"output\": \" InChI=1S/C7H12/c1-2-4-6-7-5-3-1/h1-2H,3-7H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][O][C][=Branch1][C][=O][NH1][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Chlorzoxazone\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" p-Chloroacetanilide\\n\",\n        \"output\": \" InChI=1S/C8H8ClNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Eriodictyol\\n\",\n        \"output\": \" Oc2cc(O)c1C(=O)CC(Oc1c2)c3ccc(O)c(O)c3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)CCC\\n\",\n        \"output\": \" Pentobarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC=C)CC=C\\n\",\n        \"output\": \" 0.008375292821268827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzo(k)fluoranthene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Branch1][N][C][Ring1][O][=C][C][Ring1][#C][=C][Ring2][Ring1][Ring1][=C][Ring1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dimethyl phthalate\\n\",\n        \"output\": \" COC(=O)c1ccccc1C(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-4-5(2)6(3)7/h5H,4H2,1-3H3\\n\",\n        \"output\": \" 3-Methyl-2-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H4N2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H\\n\",\n        \"output\": \" Phthalonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Methylcyclohexene \\n\",\n        \"output\": \" [C][C][=C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H12/c1-8(2)9-6-4-3-5-7-9/h3-8H,1-2H3\\n\",\n        \"output\": \" Isopropylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Thalidomide\\n\",\n        \"output\": \" InChI=1S/C13H10N2O4/c16-10-6-5-9(11(17)14-10)15-12(18)7-3-1-2-4-8(7)13(15)19/h1-4,9H,5-6H2,(H,14,16,17)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 5.888436553555884e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10Cl10O/c11-2-1(21)3(12)6(15)4(2,13)8(17)5(2,14)7(3,16)9(6,18)10(8,19)20\\n\",\n        \"output\": \" -5.2589999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CH2I2/c2-1-3/h1H2\\n\",\n        \"output\": \" Diiodomethane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" -3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 4-Heptanone\\n\",\n        \"output\": \" InChI=1S/C7H14O/c1-3-5-7(8)6-4-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COC(=O)c1ccccc1\\n\",\n        \"output\": \" Methyl benzoate \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-6(2)5-7(3,4)8/h6,8H,5H2,1-4H3\\n\",\n        \"output\": \" 2,4-Dimethyl-2-pentanol \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nitrofen\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][P][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][P]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" C1c2ccccc2c3ccc4ccccc4c13\\n\",\n        \"output\": \" -6.68\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" greek\\n\",\n        \"output\": \" greek does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 1-Pentadecanol\\n\",\n        \"output\": \" 4.466835921509635e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C11H13F3N2O3S/c1-6-4-7(2)10(5-9(6)15-8(3)17)16-20(18,19)11(12,13)14/h4-5,16H,1-3H3,(H,15,17)\\n\",\n        \"output\": \" -3.24\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Phenylhydrazine\\n\",\n        \"output\": \" 0.07\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl formate\\n\",\n        \"output\": \" InChI=1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][S][Branch1][C][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" oryzalin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Estragole\\n\",\n        \"output\": \" InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3,5-8H,1,4H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Betamethasone-17-valerate\\n\",\n        \"output\": \" CCCCC(=O)OC3(C(C)CC4C2CCC1=CC(=O)C=CC1(C)C2(F)C(O)CC34C)C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" D-fenchone\\n\",\n        \"output\": \" InChI=1S/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5N3/c1-2-4-6-5(3-1)7-9-8-6/h1-4H,(H,7,8,9)\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Medrogestone\\n\",\n        \"output\": \" 5.370317963702533e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Cyclooctyl-5-spirobarbituric acid\\n\",\n        \"output\": \" 0.0010423174293933046 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Iodofenphos\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][I][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Sparsomycin (3,8mg/ml)\\n\",\n        \"output\": \" InChI=1S/C13H19N3O5S2/c1-8-10(12(19)16-13(20)14-8)3-4-11(18)15-9(5-17)6-23(21)7-22-2/h3-4,9,17H,5-7H2,1-2H3,(H,15,18)(H2,14,16,19,20)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Dimethyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Cyclooctane\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Dyphylline\\n\",\n        \"output\": \" -0.17\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Oc1cccc(Cl)c1Cl\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=Branch1][N][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" Propetamphos\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Monolinuron\\n\",\n        \"output\": \" 0.0026915348039269166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" hexacosane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" ClC=C\\n\",\n        \"output\": \" 0.01778279410038923 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCC1(CCC(C)C)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" 0.003404081897010009 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-3-4-8(9)5-7(6)2/h3-5,9H,1-2H3\\n\",\n        \"output\": \" 3,4-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" law\\n\",\n        \"output\": \" law does not have solubility.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" c1(Br)c(Br)cc(Br)cc1\\n\",\n        \"output\": \" -4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClCC#CCOC(=O)Nc1cccc(Cl)c1\\n\",\n        \"output\": \" Barban\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-16H,3-10H2,1-2H3\\n\",\n        \"output\": \" Androstenedione\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3\\n\",\n        \"output\": \" 0.004265795188015926 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6HCl5O/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H\\n\",\n        \"output\": \" -4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Cl]\\n\",\n        \"output\": \" 0.523\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCC(=O)C\\n\",\n        \"output\": \" -2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-Napthol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" -6.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O]\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -1.827\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Chloroxuron\\n\",\n        \"output\": \" 1.2882495516931348e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][Ring1][C][C][C][O]\\n\",\n        \"output\": \" 2-Ethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CNC(=O)Oc1cccc2ccccc12\\n\",\n        \"output\": \" Carbaryl\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzaldehyde\\n\",\n        \"output\": \" [O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Pentene \\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Dicapthon\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,1,2-Trichlorotrifluoroethane\\n\",\n        \"output\": \" InChI=1S/C2Cl3F3/c3-1(4,6)2(5,7)8\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC(=O)C\\n\",\n        \"output\": \" Ethyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methyl nonanoate\\n\",\n        \"output\": \" CCCCCCCCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCO\\n\",\n        \"output\": \" 1-Heptanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" 3-Methyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC(=O)CC(=O)OCC\\n\",\n        \"output\": \" Malonic acid diethylester\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCC(=O)OC\\n\",\n        \"output\": \" Methyl hexanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" P,P'-DDE\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" Epiandrosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.0003311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-3-4-5(2)6/h3-4H2,1-2H3\\n\",\n        \"output\": \" 2-Pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 2-Heptanol \\n\",\n        \"output\": \" -1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Nitrazepam\\n\",\n        \"output\": \" InChI=1S/C15H11N3O3/c19-14-9-16-15(10-4-2-1-3-5-10)12-8-11(18(20)21)6-7-13(12)17-14/h1-8H,9H2,(H,17,19)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Brc1cccc(Br)c1\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Butethal\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][#Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H14ClNS2/c1-4-10(5-2)8(11)12-6-7(3)9/h3-6H2,1-2H3\\n\",\n        \"output\": \" Sulfallate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benznidazole\\n\",\n        \"output\": \" O=C(Cn1ccnc1N(=O)=O)NCc2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H10INO/c14-12-9-5-4-8-11(12)13(16)15-10-6-2-1-3-7-10/h1-9H,(H,15,16)\\n\",\n        \"output\": \" benodanil\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1c(NC(=O)c2ccccc2(I))cccc1\\n\",\n        \"output\": \" benodanil\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Heptene\\n\",\n        \"output\": \" [C][C][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Br]\\n\",\n        \"output\": \" Bromochloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3\\n\",\n        \"output\": \" Estrone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" ethyl cinnamate\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" p-Nitrotoluene\\n\",\n        \"output\": \" 0.003235936569296281 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H18ClN5/c1-5-16(6-2)10-14-8(11)13-9(15-10)12-7(3)4/h7H,5-6H2,1-4H3,(H,12,13,14,15)\\n\",\n        \"output\": \" -3.785\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5,5-Dimethylbarbituric acid\\n\",\n        \"output\": \" InChI=1S/C6H8N2O3/c1-6(2)3(9)7-5(11)8-4(6)10/h1-2H3,(H2,7,8,9,10,11)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=N(=O)c1ccccc1\\n\",\n        \"output\": \" Nitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3\\n\",\n        \"output\": \" -0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1-Nitropropane\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3\\n\",\n        \"output\": \" 1-Nonene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCSSCC\\n\",\n        \"output\": \" Diethyldisulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Propanil\\n\",\n        \"output\": \" [C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc2c(c1)[nH]c3ccccc32\\n\",\n        \"output\": \" Carbazole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its oil solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" cis-2-Pentene\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Clc2ccc1oc(=O)[nH]c1c2\\n\",\n        \"output\": \" -2.8310000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14O5/c1-18-8-5-10(16)13-12(6-8)19-11-3-2-7(15)4-9(11)14(13)17/h2-6,9,11-13,15-16H,1H3\\n\",\n        \"output\": \" gentisin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" butacarb\\n\",\n        \"output\": \" c1(C(C)(C)C)cc(C(C)(C)C)cc(OC(=O)NC)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cccc2c(C)cccc12\\n\",\n        \"output\": \" 1,5-Dimethlnapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Dicofol\\n\",\n        \"output\": \" -5.666\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H6S/c7-6-4-2-1-3-5-6/h1-5,7H\\n\",\n        \"output\": \" Thiophenol \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 4-Bromotoluene\\n\",\n        \"output\": \" 0.0006456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" -3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2,4,6-Trinitrotoluene\\n\",\n        \"output\": \" 0.0006025595860743575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Br2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" 1,3-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dyphylline\\n\",\n        \"output\": \" InChI=1S/C10H14N4O4/c1-12-8-7(9(17)13(2)10(12)18)14(5-11-8)3-6(16)4-15/h5-6,15-16H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H7Cl3O2/c13-7-1-3-11(9(15)5-7)17-12-4-2-8(14)6-10(12)16/h1-6,16H\\n\",\n        \"output\": \" Triclosan\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nitrobenzene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3\\n\",\n        \"output\": \" -4.25\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 8.128305161640995e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Triallate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][Branch1][C][Cl][=C][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Isopropyl acetate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1Cc2ccccc2C1\\n\",\n        \"output\": \" Indan\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Mefenacet\\n\",\n        \"output\": \" InChI=1S/C16H14N2O2S/c1-18(12-7-3-2-4-8-12)15(19)11-20-16-17-13-9-5-6-10-14(13)21-16/h2-10H,11H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Acetophenone\\n\",\n        \"output\": \" CC(=O)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,4,6-Trichlorophenol\\n\",\n        \"output\": \" Oc1c(Cl)cc(Cl)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H3Cl7/c13-4-1-2-6(14)5(3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\\n\",\n        \"output\": \" 1.148153621496884e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccc(C)c(C)c1\\n\",\n        \"output\": \" 1,2,4-Trimethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCC1(CC)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" 0.021827299118430014 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Anilofos\\n\",\n        \"output\": \" COP(=S)(OC)SCC(=O)N(C(C)C)c1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 3-Methylbutan-1-ol\\n\",\n        \"output\": \" 0.30902954325135906 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" OC3N=C(c1ccccc1Cl)c2cc(Cl)ccc2NC3=O\\n\",\n        \"output\": \" 0.0002488857318282393 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Ethyl heptanoate\\n\",\n        \"output\": \" -2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][Ring2][O][Ring1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 0.00032136605386403147 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" m-Chloroiodobenzene\\n\",\n        \"output\": \" Clc1cccc(I)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 9,10-Dimethylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" L-arabinose\\n\",\n        \"output\": \" [C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)Nc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 0.002032357010936223 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-5-7(3,4)6-2/h5-6H2,1-4H3\\n\",\n        \"output\": \" 3,3-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Biphenyl\\n\",\n        \"output\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][=Branch1][#Branch2][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Azobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H8BrCl2O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\\n\",\n        \"output\": \" Bromophos\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3\\n\",\n        \"output\": \" 4.775292736576902e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" DEF\\n\",\n        \"output\": \" InChI=1S/C12H27OPS3/c1-4-7-10-15-14(13,16-11-8-5-2)17-12-9-6-3/h4-12H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H9N3O3/c1-5-7-4-6(9(11)12)8(5)2-3-10/h4,10H,2-3H2,1H3\\n\",\n        \"output\": \" Metronidazole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COC=O\\n\",\n        \"output\": \" Methyl formate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Dieldrin\\n\",\n        \"output\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Picene\\n\",\n        \"output\": \" c1ccc2c(c1)ccc3c2ccc4c5ccccc5ccc43\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][N][=C][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.3988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4-Ethyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" date\\n\",\n        \"output\": \" date does not have InChI\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4-Isopropyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H14N2O2/c1-2-12(9-6-4-3-5-7-9)10(15)13-8-14-11(12)16/h3-7H,2,8H2,1H3,(H,13,15)(H,14,16)\\n\",\n        \"output\": \" 0.0022908676527677724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3,3-Dimethylpentane\\n\",\n        \"output\": \" CCC(C)(C)CC\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Hexanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" m-Nitroaniline\\n\",\n        \"output\": \" InChI=1S/C6H6N2O2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H,7H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CNC(=O)Oc1cccc(N=CN(C)C)c1\\n\",\n        \"output\": \" Formetanate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5I/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" -3.01\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\\n\",\n        \"output\": \" -4.38\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1N(COC(=O)CC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3-Propanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][=O]\\n\",\n        \"output\": \" 0.007413102413009177 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Chlordane\\n\",\n        \"output\": \" [Cl][C][C][C][C][Branch1][Branch1][C][Ring1][Branch1][Cl][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Iodopropane\\n\",\n        \"output\": \" CC(C)I\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][Branch1][C][O][=C][C][Branch1][C][O][=C][C][=C][Ring1][Branch2][C][C][C][C][C][C]\\n\",\n        \"output\": \" 4-hexylresorcinol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C)CC=C\\n\",\n        \"output\": \" 5-Allyl-5-methylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,6-Dimethylnaphthalene \\n\",\n        \"output\": \" InChI=1S/C12H12/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Di-n-propylsulfide\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4F2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\",\n        \"output\": \" -1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1,3-Dimethylnaphthalene\\n\",\n        \"output\": \" -4.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C][=C]\\n\",\n        \"output\": \" 0.06918309709189366 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Diphenyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its oil solubility expressed as a logarithm in mol/L. ->\",\n        \"input\": \" InChI=1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Primidone\\n\",\n        \"output\": \" -2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Heptene\\n\",\n        \"output\": \" CCCCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Benzamide\\n\",\n        \"output\": \" InChI=1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\\n\",\n        \"output\": \" 0.00038018939632056124 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methyl-1-Pentene\\n\",\n        \"output\": \" [C][C][C][C][=Branch1][C][=C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" C1C=CCC=C1\\n\",\n        \"output\": \" 0.008709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.44\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][C][Br]\\n\",\n        \"output\": \" -1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethanethiol\\n\",\n        \"output\": \" [C][C][S]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Chlorthalidone\\n\",\n        \"output\": \" -3.451\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" C1Cc2c3c1cccc3cc4c2ccc5ccccc54\\n\",\n        \"output\": \" -7.85\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3/b3-2+\\n\",\n        \"output\": \" t-Crotonaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC(C)C(C)C\\n\",\n        \"output\": \" 2,3-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Propylene\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][P][C][=Branch1][Ring1][=C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Dienestrol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" Urea\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methylbutanol\\n\",\n        \"output\": \" CCC(C)CO\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C3H6Cl2/c4-2-1-3-5/h1-3H2\\n\",\n        \"output\": \" 0.023988329190194897 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][Branch1][C][O][C][C][Ring1][P][Ring2][Ring1][Branch1][C]\\n\",\n        \"output\": \" 1.3182567385564074e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-2-3-4-5-6/h5H,2-4H2,1H3\\n\",\n        \"output\": \" Valeraldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Corticosterone\\n\",\n        \"output\": \" InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methylpropan-1-ol\\n\",\n        \"output\": \" InChI=1S/C4H10O/c1-4(2)3-5/h4-5H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Methyl-3-heptanol\\n\",\n        \"output\": \" CCCCC(C)(O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Fenoxycarb\\n\",\n        \"output\": \" InChI=1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Nc1ccc(cc1)S(=O)(=O)c2ccc(N)cc2\\n\",\n        \"output\": \" 0.0008053784411990669 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-3-4-5(6)7-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" Propyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Hexyne\\n\",\n        \"output\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccc2ccccc2c1\\n\",\n        \"output\": \" Napthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCC(O)C=C\\n\",\n        \"output\": \" -0.59\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Phenytoin\\n\",\n        \"output\": \" O=C1NC(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,5-Dimethlnapthalene\\n\",\n        \"output\": \" 2.0941124558508955e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H14NO4PS/c1-3-16-18(19,17-4-2)13-11(14)9-7-5-6-8-10(9)12(13)15/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" -3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Tetrafluthrin\\n\",\n        \"output\": \" Cc1c(F)c(F)c(COC(=O)C2C(C=C(Cl)C(F)(F)F)C2(C)C)c(F)c1F\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,3-Dichloropropane\\n\",\n        \"output\": \" [Cl][C][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 3,5-Dimethylpyridine\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][N][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -3.4989999999999997\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][Branch1][Ring1][C][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/CH3Br/c1-2/h1H3\\n\",\n        \"output\": \" -0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 0.018197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Dimethoxymethane\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" p-benzidine\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][Branch1][C][O][C][C][Ring1][P][Ring2][Ring1][Branch1][C]\\n\",\n        \"output\": \" Hydrocortisone 21-acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Pentylcyclopentane\\n\",\n        \"output\": \" CCCCCC1CCCC1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H\\n\",\n        \"output\": \" -0.17\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Medrogestone\\n\",\n        \"output\": \" InChI=1S/C23H32O2/c1-14-12-17-18(21(3)9-6-16(25)13-20(14)21)7-11-23(5)19(17)8-10-22(23,4)15(2)24/h12-13,17-19H,6-11H2,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Hexachloroethane\\n\",\n        \"output\": \" ClC(Cl)(Cl)C(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Isoquinoline\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 2-Methylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Methocarbamol\\n\",\n        \"output\": \" -0.985\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,1-Dichloroethane\\n\",\n        \"output\": \" CC(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methyl benzoate \\n\",\n        \"output\": \" InChI=1S/C8H8O2/c1-10-8(9)7-5-3-2-4-6-7/h2-6H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Buthidazole\\n\",\n        \"output\": \" -1.8769999999999998\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCC\\n\",\n        \"output\": \" Octane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Clc1ccc(I)cc1\\n\",\n        \"output\": \" -4.03\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,3-Dichlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][#C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][Branch2][=O][C][=C][C][C][C][C][C][Ring1][#Branch1][C][Ring1][Branch1]\\n\",\n        \"output\": \" 0.0020137242498623874 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC/C=C/C\\n\",\n        \"output\": \" trans-2-Heptene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Methyl-1-Butene\\n\",\n        \"output\": \" CC(C)C=C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3\\n\",\n        \"output\": \" Ethyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCCOC(=O)CC\\n\",\n        \"output\": \" 0.15135612484362082 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,6-Dimethylphenol\\n\",\n        \"output\": \" Cc1cccc(C)c1O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][N][=C][N][Ring1][Branch1][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.8407720014689545e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" -2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Terbumeton\\n\",\n        \"output\": \" -3.239\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Succinimide\\n\",\n        \"output\": \" InChI=1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC1=C(C(=O)Nc2ccccc2)S(=O)(=O)CCO1\\n\",\n        \"output\": \" 0.0052360043658575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 0.00018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" -6.57\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H5ClO/c7-5-1-3-6(8)4-2-5/h1-4,8H\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Pentanol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-2-3-4-5-6/h6H,2-5H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3/c7-4-1-2-5(8)6(9)3-4/h1-3H\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-5-6(7)4-2/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 3-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" -5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Indan\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][N][=N][C][Ring1][=N][=N][Ring2][Ring1][C]\\n\",\n        \"output\": \" 0.003944573020752785 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" 0.015848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3\\n\",\n        \"output\": \" -2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Nitrazepam\\n\",\n        \"output\": \" O=C3CN=C(c1ccccc1)c2cc(ccc2N3)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][Branch2][Ring1][=Branch1][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][Branch2][=O]\\n\",\n        \"output\": \" 1.1721953655481303e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" ClC=C(Cl)Cl\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][C][Branch1][C][O][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCC(=O)OC\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCNc1nc(Cl)nc(n1)N(CC)CC\\n\",\n        \"output\": \" Trietazine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" Androstenedione\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Methyl pentanoate\\n\",\n        \"output\": \" InChI=1S/C6H12O2/c1-3-5-6(7)8-4-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][S][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Diisopropylsulfide\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COP(=O)(OC)C(O)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H19N5O/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" Prometon\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" N,N-Dimethylaniline\\n\",\n        \"output\": \" CN(C)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Benzotriazole\\n\",\n        \"output\": \" InChI=1S/C6H5N3/c1-2-4-6-5(3-1)7-9-8-6/h1-4H,(H,7,8,9)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC12CCC3C(CCc4cc(O)ccc34)C2CCC1O\\n\",\n        \"output\": \" Estradiol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Ethyltoluene\\n\",\n        \"output\": \" InChI=1S/C9H12/c1-3-9-7-5-4-6-8(9)2/h4-7H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Napthylamine\\n\",\n        \"output\": \" Nc1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C16H10/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h1-10H\\n\",\n        \"output\": \" 6.668067692136218e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylphenol\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H8N2O3/c1-6(2)3(9)7-5(11)8-4(6)10/h1-2H3,(H2,7,8,9,10,11)\\n\",\n        \"output\": \" 0.018113400926196024 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-5-7(2,3)6-8/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methylpentanol\\n\",\n        \"output\": \" CCCC(C)CO\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H19ClNO5P/c1-5-12(6-2)10(13)9(11)7-8-17-18(14,15-3)16-4/h7H,5-6,8H2,1-4H3\\n\",\n        \"output\": \" 3.3342641276323497 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Abate\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][S][C][=C][C][=C][Branch1][N][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=C][Ring1][=N][C][=C][Ring2][Ring1][Ring2]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC1CCCC1\\n\",\n        \"output\": \" Propylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benzocaine\\n\",\n        \"output\": \" CCOC(=O)c1ccc(N)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][Br]\\n\",\n        \"output\": \" 1-Bromobutane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3\\n\",\n        \"output\": \" Nitroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C18H22O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,17-20H,3-4H2,1-2H3\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H22N2O/c1-13(2)11(14)12-10-8-6-4-3-5-7-9-10/h10H,3-9H2,1-2H3,(H,12,14)\\n\",\n        \"output\": \" 0.006053408747539136 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,2',3,4,4',5',6-PCB\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Br]\\n\",\n        \"output\": \" Bromoethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Flutriafol\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H17Cl2NOS/c1-7(2)13(8(3)4)10(14)15-6-9(12)5-11/h5,7-8H,6H2,1-4H3\\n\",\n        \"output\": \" 5.1760683195056706e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Ethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 5-Allyl-5-phenylbarbital\\n\",\n        \"output\": \" -2.369\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1ccc(Cl)cc1Cl\\n\",\n        \"output\": \" 2,4-Dichlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" o-Methoxyphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Carbofuran\\n\",\n        \"output\": \" CNC(=O)Oc1cccc2CC(C)(C)Oc12\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.008709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" -3.6039999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,1-Dichloroethane\\n\",\n        \"output\": \" [C][C][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 2,2-Dimethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-hydroxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Fc1ccccc1\\n\",\n        \"output\": \" -1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,1-Dichloroethylene\\n\",\n        \"output\": \" InChI=1S/C2H2Cl2/c1-2(3)4/h1H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2,3-Dimethylnaphthalene\\n\",\n        \"output\": \" 1.9054607179632484e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][O][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.00016218100973589298 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Equilenin\\n\",\n        \"output\": \" CC34CCc1c(ccc2cc(O)ccc12)C3CCC4=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" Ethyl-p-aminobenzoate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" -3.03\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Ethanol\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Epiandrosterone\\n\",\n        \"output\": \" CC34CCC1C(CCC2CC(O)CCC12C)C3CCC4=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2',3,3'-PCB\\n\",\n        \"output\": \" Clc1cccc(c1Cl)c2cccc(Cl)c2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][C][C][C][C]\\n\",\n        \"output\": \" 5-Nonanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCC(CC)C=O\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2-methoxypteridine\\n\",\n        \"output\": \" -1.11\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" m-Chloronitrobenzene \\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCC(C)O\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Triethyl phosphate\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=O][Branch1][Ring2][O][C][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Branch2][Ring1][#C][C][O][C][=Branch1][C][=O][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][#Branch2][Branch1][C][C][C][C][Branch1][C][F][=C][Ring2][Ring1][=Branch2][F]\\n\",\n        \"output\": \" 4.775292736576902e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pencycuron\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch2][Ring1][=Branch2][C][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCCCCCCCO\\n\",\n        \"output\": \" -3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" N,N-Dimethylacetamide\\n\",\n        \"output\": \" 12.882495516931343 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Androstenedione\\n\",\n        \"output\": \" InChI=1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-16H,3-10H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H21N5OS/c1-8(2)13-10-14-9(12-6-5-7-17-3)15-11(16-10)18-4/h8H,5-7H2,1-4H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" Methoproptryne\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)\\n\",\n        \"output\": \" Urea\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C22H23NO3/c1-21(2)19(22(21,3)4)20(24)26-18(14-23)15-9-8-12-17(13-15)25-16-10-6-5-7-11-16/h5-13,18-19H,1-4H3\\n\",\n        \"output\": \" -6.025\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C\\n\",\n        \"output\": \" 17a-Methyltestosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Heptanol \\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCC\\n\",\n        \"output\": \" Pentane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" 3-Hexanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCC1CCCCC1\\n\",\n        \"output\": \" -4.25\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-2-5-8-6-3-4-7-8/h8H,2-7H2,1H3\\n\",\n        \"output\": \" Propylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCOc1ccc(NC(N)=O)cc1\\n\",\n        \"output\": \" -2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2-Dichlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4Cl2/c7-5-3-1-2-4-6(5)8/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1CCc2ccccc2C1\\n\",\n        \"output\": \" 1,2,3,4-Tetrahydronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1,3-Dichloropropane\\n\",\n        \"output\": \" -1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 3,4-Dimethylphenol\\n\",\n        \"output\": \" -1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 5-Methylchrysene\\n\",\n        \"output\": \" c1cccc2c3c(C)cc4ccccc4c3ccc12\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Erythritol\\n\",\n        \"output\": \" 5.011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,4-Dibromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4Br2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COP(=O)(OC)C(O)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" Trichlorfon\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][=Branch2][C][Branch1][C][O][C][Ring1][=Branch1][O][N][C][=N][C][=C][Branch1][C][O][N][=C][N][=C][Ring1][#Branch2][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0588843655355589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C3H5N/c1-2-3-4/h2H2,1H3\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H\\n\",\n        \"output\": \" 0.006025595860743574 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" m-Nitroaniline\\n\",\n        \"output\": \" -2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Cl]\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H19NO2S/c1-14(2)13(15)17-11-7-6-10-16-12-8-4-3-5-9-12/h3-5,8-9H,6-7,10-11H2,1-2H3\\n\",\n        \"output\": \" -3.927\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC3C2CCC1(C)C=CC(=O)C(=C1C2OC3=O)C\\n\",\n        \"output\": \" Santonin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methoxychlor\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Propyl propanoate\\n\",\n        \"output\": \" [C][C][C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][Br]\\n\",\n        \"output\": \" 0.0008317637711026709 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Tetrachloroethylene\\n\",\n        \"output\": \" [Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-7-5-3-4-6-8(7)2/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 5.011872336272725e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Diphenylamine\\n\",\n        \"output\": \" N(c1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" c1c(Cl)cccc1c2ccccc2\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,2,4-Trimethylpentane\\n\",\n        \"output\": \" InChI=1S/C8H18/c1-7(2)6-8(3,4)5/h7H,6H2,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 5-Ethyl-5-phenylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C4H10S2/c1-3-5-6-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" 0.0038018939632056127 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H21O2PS3/c1-6-10-12(13,11-7-2)15-8-14-9(3,4)5/h6-8H2,1-5H3\\n\",\n        \"output\": \" 1.757923613958693e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C3H7Cl/c1-2-3-4/h2-3H2,1H3\\n\",\n        \"output\": \" 0.033884415613920256 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][Cl]\\n\",\n        \"output\": \" 0.0007585775750291836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" COc2ncc1nccnc1n2\\n\",\n        \"output\": \" 0.07762471166286916 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1cc(C)c(O)c(C)c1\\n\",\n        \"output\": \" 0.008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H2Br4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\\n\",\n        \"output\": \" -6.98\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1cc2ccc3cccc4ccc(c1)c2c34\\n\",\n        \"output\": \" 6.668067692136218e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCC#C\\n\",\n        \"output\": \" 1-Hexyne \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Dexamethasone\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Cc1c2ccccc2cc3ccccc13\\n\",\n        \"output\": \" 1.288249551693135e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 2,4,6-Trichlorophenol\\n\",\n        \"output\": \" 0.004570881896148752 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 3-Heptanoyloxymethylphenytoin\\n\",\n        \"output\": \" 5.000345349769783e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCC(C)O\\n\",\n        \"output\": \" 2-Heptanol \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Flumethasone\\n\",\n        \"output\": \" CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Thiophenol \\n\",\n        \"output\": \" -2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H19ClN4O3/c1-15(2,3)12-18-20(14(22)23-12)11-7-6-9(8-10(11)16)17-13(21)19(4)5/h6-8H,1-5H3,(H,17,21)\\n\",\n        \"output\": \" Dimefuron\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Danazol\\n\",\n        \"output\": \" [C][C][C][C][C][=N][O][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][C][C][C][C][Ring1][=N][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][Branch1][C][O][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Methylnaphthalene\\n\",\n        \"output\": \" -3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Nc2cnn(c1ccccc1)c(=O)c2Cl\\n\",\n        \"output\": \" 0.0013243415351946643 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl\\n\",\n        \"output\": \" 1.3182567385564074e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][N][=C][Branch1][Ring1][C][#N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Phoxim\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H\\n\",\n        \"output\": \" 2,3,4,6-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Cholanthrene\\n\",\n        \"output\": \" 1.4125375446227554e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-t-Butylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC34CC(O)C1(F)C(CCC2=CC(=O)C=CC12C)C3CC(O)C4(O)C(=O)CO\\n\",\n        \"output\": \" Triamcinolone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" ClCCCl\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methyl pentanoate\\n\",\n        \"output\": \" [C][C][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cc(C)cc(C)c1\\n\",\n        \"output\": \" 1,3,5-Trimethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Isopentyl formate\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Mirex\\n\",\n        \"output\": \" -6.8\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-6-7(3,8)5-2/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" 0.10471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-5-4-8-15-13(11)10-9-12-6-2-3-7-14(12)15/h2-10H,1H3\\n\",\n        \"output\": \" -5.85\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCC(C)O\\n\",\n        \"output\": \" 2-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)CC(C)(C)C\\n\",\n        \"output\": \" 2,2,4-Trimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1c2ccccc2c(C)c3ccc4ccccc4c13\\n\",\n        \"output\": \" 7,12-Dimethylbenz(a)anthracene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC(C)COC(=O)C\\n\",\n        \"output\": \" -1.21\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O]\\n\",\n        \"output\": \" 2.280342072000418 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methyldymron\\n\",\n        \"output\": \" [C][N][Branch2][Ring1][Branch1][C][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Fenpropathrin\\n\",\n        \"output\": \" 9.440608762859226e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][N][=C][Branch1][Ring1][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C]\\n\",\n        \"output\": \" Oxamyl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClCC#N\\n\",\n        \"output\": \" Chloroacetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OCC2OC(Oc1ccccc1CO)C(O)C(O)C2O\\n\",\n        \"output\": \" Salicin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" NC(=O)c1ccccc1O\\n\",\n        \"output\": \" -1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" ClCC(Cl)Cl\\n\",\n        \"output\": \" 0.03311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Trichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1CCC(=O)N1\\n\",\n        \"output\": \" Succinimide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H17Br/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3\\n\",\n        \"output\": \" 1-Bromooctane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Nonanol\\n\",\n        \"output\": \" InChI=1S/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H26O12/c1-27-17(26)8-4-2-3-5-10(8)30-19-16(25)14(23)13(22)11(31-19)7-29-18-15(24)12(21)9(20)6-28-18/h2-5,9,11-16,18-25H,6-7H2,1H3\\n\",\n        \"output\": \" Monotropitoside\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][O][N][C][Branch1][C][C][Branch1][C][C][C][#N][=N][Ring1][=N]\\n\",\n        \"output\": \" Cyanazine\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methylbutanol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Clc1cc(Cl)cc(Cl)c1\\n\",\n        \"output\": \" 1,3,5-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Prometon\\n\",\n        \"output\": \" -2.478\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Butene\\n\",\n        \"output\": \" 0.01148153621496883 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" cis-2-Pentene\\n\",\n        \"output\": \" CC/C=C\\\\C\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 3-Methylphenol\\n\",\n        \"output\": \" -0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pentylbenzene\\n\",\n        \"output\": \" InChI=1S/C11H16/c1-2-3-5-8-11-9-6-4-7-10-11/h4,6-7,9-10H,2-3,5,8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Tetrahydrofurane \\n\",\n        \"output\": \" C1CCOC1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Fluorometuron\\n\",\n        \"output\": \" 0.00047863009232263854 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1c(O)C2C(=O)C3cc(O)ccC3OC2cc1(OC)\\n\",\n        \"output\": \" gentisin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Flucytosine\\n\",\n        \"output\": \" InChI=1S/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCCCCCCCCCCC\\n\",\n        \"output\": \" -8.334\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its oil solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][S][C][=C][C][=C][Branch1][N][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=C][Ring1][=N][C][=C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p,p'-Biphenyldiamine \\n\",\n        \"output\": \" InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccc2cc3c4cccc5cccc(c3cc2c1)c45\\n\",\n        \"output\": \" Benzo(k)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Pentylcyclopentane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H2Cl4/c3-1-2(4,5)6/h1H2\\n\",\n        \"output\": \" 1,1,1,2-Tetrachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H6N4/c1-5-2-9-6-3-8-4-10-7(6)11-5/h2-4H,1H3\\n\",\n        \"output\": \" 7-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" -8.176\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3\\n\",\n        \"output\": \" 2,4,6-Trimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCOC(=O)c1ccc(O)cc1\\n\",\n        \"output\": \" 0.0044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H16O/c1-3-4-5-6-7-8(2)9/h3-7H2,1-2H3\\n\",\n        \"output\": \" -2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chloropham\\n\",\n        \"output\": \" CC(C)OC(=O)Nc1cccc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" Diisopropyl ether \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0005011872336272725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3\\n\",\n        \"output\": \" -2.32\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)CC\\n\",\n        \"output\": \" Butabarbital\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Heptanone\\n\",\n        \"output\": \" CCCCCC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][O][C][C][C]\\n\",\n        \"output\": \" Dipropyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Xipamide\\n\",\n        \"output\": \" -3.79\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=N][C][=Branch1][#Branch2][=N][C][Branch1][C][C][=C][Ring1][#Branch1][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.011220184543019636 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)N\\n\",\n        \"output\": \" p-Toluenesulfonamide \\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Benzene \\n\",\n        \"output\": \" InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCOCCOCC\\n\",\n        \"output\": \" -0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" Triphenylene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -4.53\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" Diphenyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Cyclopentene \\n\",\n        \"output\": \" -2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Ethyl-2-hexanal\\n\",\n        \"output\": \" InChI=1S/C8H14O/c1-3-5-6-8(4-2)7-9/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc2ccc1oc(=O)c(Cl)c(C)c1c2\\n\",\n        \"output\": \" Coumaphos\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propylisopropylether\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-4-5-7-6(2)3/h6H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Bromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C][C][C]\\n\",\n        \"output\": \" dibutyl sebacate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Triallate\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CC\\n\",\n        \"output\": \" -2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dialifos\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=N(=O)c1ccccc1N(=O)=O\\n\",\n        \"output\": \" 1,2-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCc1ccc2ccccc2c1\\n\",\n        \"output\": \" 2-Ethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H\\n\",\n        \"output\": \" Quinoline\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Coumachlor\\n\",\n        \"output\": \" InChI=1S/C19H15ClO4/c1-11(21)10-15(12-6-8-13(20)9-7-12)17-18(22)14-4-2-3-5-16(14)24-19(17)23/h2-9,15,22H,10H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Betamethasone-17-valerate\\n\",\n        \"output\": \" InChI=1S/C27H37FO6/c1-5-6-7-23(33)34-27(22(32)15-29)16(2)12-20-19-9-8-17-13-18(30)10-11-24(17,3)26(19,28)21(31)14-25(20,27)4/h10-11,13,16,19-21,29,31H,5-9,12,14-15H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Methyltetrahydrofurane\\n\",\n        \"output\": \" CC1CCCO1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pentobarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Oc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" -4.28\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,4-Dinitrotoluene\\n\",\n        \"output\": \" InChI=1S/C7H6N2O4/c1-5-2-3-6(8(10)11)4-7(5)9(12)13/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" p-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H13Cl/c1-2-3-4-5-6-7/h2-6H2,1H3\\n\",\n        \"output\": \" 1-Chlorohexane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,3,5-Trimethylbenzene \\n\",\n        \"output\": \" Cc1cc(C)cc(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6)\\n\",\n        \"output\": \" 11.748975549395297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][=C][C][C][C][Branch1][C][C][=C][C][=O]\\n\",\n        \"output\": \" citral\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=O][Branch1][Ring2][O][C][C][O][C][C]\\n\",\n        \"output\": \" Triethyl phosphate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Branch2][C][Branch1][C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" Secobarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2ccc(F)c(Oc3ccccc3)c2\\n\",\n        \"output\": \" Cyfluthrin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Dienestrol\\n\",\n        \"output\": \" InChI=1S/C18H18O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h3-12,19-20H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][#C][C][C]\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" 3.881503659906478e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nitramine\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2,3,4-Tetrachlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H2Cl4/c7-3-1-2-4(8)6(10)5(3)9/h1-2H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][C][=C]\\n\",\n        \"output\": \" 5,5-Diallylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCN(=O)=O\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Piperophos\\n\",\n        \"output\": \" InChI=1S/C14H28NO3PS2/c1-4-10-17-19(20,18-11-5-2)21-12-14(16)15-9-7-6-8-13(15)3/h13H,4-12H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pencycuron\\n\",\n        \"output\": \" Clc1ccc(CN(C2CCCC2)C(=O)Nc3ccccc3)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" Ronnel\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H34O3/c1-15(2)22-18(20)14-17(4)11-8-10-16(3)12-9-13-19(5,6)21-7/h8,11,14-16H,9-10,12-13H2,1-7H3\\n\",\n        \"output\": \" Methoprene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" C1CCC=CC1\\n\",\n        \"output\": \" -2.59\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dicapthon\\n\",\n        \"output\": \" COP(=S)(OC)Oc1ccc(cc1Cl)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" benodanil\\n\",\n        \"output\": \" c1c(NC(=O)c2ccccc2(I))cccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H6N2O2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H,7H2\\n\",\n        \"output\": \" o-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Urea\\n\",\n        \"output\": \" InChI=1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [N][=Branch1][#Branch2][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.45\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Benfluralin\\n\",\n        \"output\": \" -5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" m-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Etoposide (148-167,25mg/ml)\\n\",\n        \"output\": \" COc1cc(cc(OC)c1O)C6C2C(COC2=O)C(OC4OC3COC(C)OC3C(O)C4O)c7cc5OCOc5cc67\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCN(CC)C(=O)CSc1ccc(Cl)nn1\\n\",\n        \"output\": \" 0.019230917289101587 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" N#Cc1ccccc1\\n\",\n        \"output\": \" Benzonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2H3Cl3/c3-1-2(4)5/h2H,1H2\\n\",\n        \"output\": \" -1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][Ring1][Ring1][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][Branch2][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Oc2cc(O)c1C(=O)CC(Oc1c2)c3ccc(O)c(O)c3\\n\",\n        \"output\": \" -3.62\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Bromonapthalene\\n\",\n        \"output\": \" Brc1ccc2ccccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClC(Cl)(Cl)Cl\\n\",\n        \"output\": \" Tetrachloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 4-Ethyltoluene\\n\",\n        \"output\": \" -3.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its oil solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC1(C)C2CCC1(C)C(O)C2\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benzophenone\\n\",\n        \"output\": \" O=C(c1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)C(C)C)N(=O)=O\\n\",\n        \"output\": \" Isopropalin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3,5-8H,1,4H2,2H3\\n\",\n        \"output\": \" Estragole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Pentane\\n\",\n        \"output\": \" [C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Amitraz\\n\",\n        \"output\": \" InChI=1S/C19H23N3/c1-14-6-8-18(16(3)10-14)20-12-22(5)13-21-19-9-7-15(2)11-17(19)4/h6-13H,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Danazol\\n\",\n        \"output\": \" InChI=1S/C22H27NO2/c1-4-22(24)10-8-18-16-6-5-15-11-19-14(13-23-25-19)12-20(15,2)17(16)7-9-21(18,22)3/h1,11,13,16-18,24H,5-10,12H2,2-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Bromotoluene\\n\",\n        \"output\": \" -2.23\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" hexacosane\\n\",\n        \"output\": \" CCCCCCCCCCCCCCCCCCCCCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][N][C][C][N][Ring1][Branch1][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.0006025595860743575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" p-Chloroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=N][C][=N][C][=N][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.466\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H21O4P/c1-16-11-13-19(14-12-16)23-26(22,24-20-9-6-7-17(2)15-20)25-21-10-5-4-8-18(21)3/h4-15H,1-3H3\\n\",\n        \"output\": \" Tricresyl phosphate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)I\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1c2ccccc2C(=O)c3ccccc13\\n\",\n        \"output\": \" -5.19\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" -4.69\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Fenoxycarb\\n\",\n        \"output\": \" CCOC(=O)NCCOc2ccc(Oc1ccccc1)cc2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Methyldymron\\n\",\n        \"output\": \" 0.00044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H6S/c7-6-4-2-1-3-5-6/h1-5,7H\\n\",\n        \"output\": \" -2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3\\n\",\n        \"output\": \" 1,2-Dichloropropane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Chloro-2-bromoethane\\n\",\n        \"output\": \" InChI=1S/C2H4BrCl/c3-1-2-4/h1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-methyluracil\\n\",\n        \"output\": \" Cn1ccc(=O)[nH]c1=O\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCCO\\n\",\n        \"output\": \" 4.168693834703354 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" C1CCC=CCC1\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1CCOC1\\n\",\n        \"output\": \" Tetrahydrofurane \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][C][C][=C]\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Terbacil\\n\",\n        \"output\": \" InChI=1S/C9H13ClN2O2/c1-5-6(10)7(13)12(8(14)11-5)9(2,3)4/h1-4H3,(H,11,14)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" benzoin\\n\",\n        \"output\": \" 0.001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 9.120108393559096e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCOP(=S)(OCC)N2C(=O)c1ccccc1C2=O\\n\",\n        \"output\": \" -3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][P][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][P]\\n\",\n        \"output\": \" Nitrofen\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CBr4/c2-1(3,4)5\\n\",\n        \"output\": \" -3.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][/C][=C][\\\\C]\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][S][C][C][C]\\n\",\n        \"output\": \" Di-n-propylsulfide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Bromonapthalene\\n\",\n        \"output\": \" InChI=1S/C10H7Br/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-5-6(2,3)7/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1c(C)c2c3ccccc3ccc2c4ccccc14\\n\",\n        \"output\": \" 5,6-Dimethylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(C)(C)O\\n\",\n        \"output\": \" 2-Methylbutan-2-ol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 2,2-Dimethylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 3-Methylheptane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Phenylthiourea\\n\",\n        \"output\": \" [N][C][=Branch1][C][=S][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Brc1ccc(I)cc1\\n\",\n        \"output\": \" 2.754228703338169e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Flumetralin\\n\",\n        \"output\": \" CCN(Cc1c(F)cccc1Cl)c2c(cc(cc2N(=O)=O)C(F)(F)F)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Chlorobiphenyl\\n\",\n        \"output\": \" Clc1ccccc1c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" m-Nitroaniline\\n\",\n        \"output\": \" [N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-pyrrolidone\\n\",\n        \"output\": \" O=C1CCCN1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 0.057543993733715694 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCOCCC\\n\",\n        \"output\": \" -1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H9ClF2N2O2/c15-8-4-6-9(7-5-8)18-14(21)19-13(20)12-10(16)2-1-3-11(12)17/h1-7H,(H2,18,19,20,21)\\n\",\n        \"output\": \" difluron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C]\\n\",\n        \"output\": \" -1.7080000000000002\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Methyl octanoate\\n\",\n        \"output\": \" 0.0006760829753919819 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H7Cl2NO3/c13-8-1-6-12(11(14)7-8)18-10-4-2-9(3-5-10)15(16)17/h1-7H\\n\",\n        \"output\": \" Nitrofen\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" -2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" COC(=O)c1ccc(O)cc1\\n\",\n        \"output\": \" 0.014893610777109155 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1cc(C)cc2c1c3cc4cccc5CCc(c45)c3cc2\\n\",\n        \"output\": \" 3-Methylcholanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Carvacrol\\n\",\n        \"output\": \" [C][Branch1][C][O][=C][Branch1][C][C][C][=C][C][Branch1][=Branch1][C][Branch1][C][C][C][=C][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2\\n\",\n        \"output\": \" Cyclohexanone\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Hexylbenzene \\n\",\n        \"output\": \" InChI=1S/C12H18/c1-2-3-4-6-9-12-10-7-5-8-11-12/h5,7-8,10-11H,2-4,6,9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=C)C\\n\",\n        \"output\": \" 2-Methylpropene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Butethal\\n\",\n        \"output\": \" InChI=1S/C10H16N2O3/c1-3-5-6-10(4-2)7(13)11-9(15)12-8(10)14/h3-6H2,1-2H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C]\\n\",\n        \"output\": \" 1,2-Diethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" kebuzone\\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,6-Dimethylnaphthalene \\n\",\n        \"output\": \" Cc1ccc2cc(C)ccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Methyl hexanoate\\n\",\n        \"output\": \" CCCCCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" ClCC(C)C\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Butylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H11Br/c1-2-3-4-5-6/h2-5H2,1H3\\n\",\n        \"output\": \" 1-Bromopentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Chloropropane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" COc2cnc1ncncc1n2\\n\",\n        \"output\": \" 0.07261059574351547 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" ClC(Cl)C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" -7.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [S][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Thiophenol \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCCC(C)O\\n\",\n        \"output\": \" 0.5128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)\\n\",\n        \"output\": \" Mebendazole\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Santonin\\n\",\n        \"output\": \" CC3C2CCC1(C)C=CC(=O)C(=C1C2OC3=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Phenetole\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Carvone\\n\",\n        \"output\": \" CC(=C)C1CC=C(C)C(=O)C1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,4-Dimethylpentane\\n\",\n        \"output\": \" CC(C)CC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Decene\\n\",\n        \"output\": \" CCCCCCCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanol\\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Diethyl sulfide\\n\",\n        \"output\": \" InChI=1S/C4H10S/c1-3-5-4-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propyl butyrate\\n\",\n        \"output\": \" InChI=1S/C5H10O2/c1-3-4-5(6)7-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H10N2O3/c11-5-8(3-1-2-4-8)6(12)10-7(13)9-5/h1-4H2,(H2,9,10,11,12,13)\\n\",\n        \"output\": \" Cyclopentyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1.445439770745928e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.77\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][Br]\\n\",\n        \"output\": \" -2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" 0.21877616239495523 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" m-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Quintozene\\n\",\n        \"output\": \" Clc1c(Cl)c(Cl)c(N(=O)=O)c(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" -3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" d-inositol\\n\",\n        \"output\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1ccc(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" 1,2,3,4-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3,4-Dichloronitrobenzene\\n\",\n        \"output\": \" O=N(=O)c1cc(Cl)c(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Undecanol\\n\",\n        \"output\": \" InChI=1S/C11H24O/c1-3-4-5-6-7-8-9-10-11(2)12/h11-12H,3-10H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C]\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Heptachlor\\n\",\n        \"output\": \" [Cl][C][C][=C][C][C][Ring1][Branch1][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cccc2ccccc12\\n\",\n        \"output\": \" 1-Methylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,2-Dimethylpentane\\n\",\n        \"output\": \" CCCC(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C23H32O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h10,16-18,20,26,28H,4-9,11-12H2,1-3H3\\n\",\n        \"output\": \" 1.3182567385564074e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Clc1cccc(n1)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" -3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Terbufos\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H18/c1-6(2)8(5)7(3)4/h6-8H,1-5H3\\n\",\n        \"output\": \" 2,3,4-Trimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C\\n\",\n        \"output\": \" 0.00038018939632056124 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2-Methylphenol\\n\",\n        \"output\": \" 0.23988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO\\n\",\n        \"output\": \" -3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COC(=O)C\\n\",\n        \"output\": \" Methyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][O][C][O][C]\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2,4,5-Tetramethylbenzene\\n\",\n        \"output\": \" InChI=1S/C10H14/c1-7-5-9(3)10(4)6-8(7)2/h5-6H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H3Cl7/c13-4-1-2-6(14)5(3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\\n\",\n        \"output\": \" 2,2',3,4,5,5',6-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C16H13N3O3/c1-18-14-8-7-12(19(21)22)9-13(14)16(17-10-15(18)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\\n\",\n        \"output\": \" -3.7960000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Bromoheptane\\n\",\n        \"output\": \" InChI=1S/C7H15Br/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyanazine\\n\",\n        \"output\": \" InChI=1S/C9H13ClN6/c1-4-12-7-13-6(10)14-8(15-7)16-9(2,3)5-11/h4H2,1-3H3,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Methyl pentanoate\\n\",\n        \"output\": \" CCCC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][C][=C][Branch1][#Branch1][O][C][Branch1][C][F][F][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Flucythrinate\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Fluoranthene\\n\",\n        \"output\": \" InChI=1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Clc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" -3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Androsterone\\n\",\n        \"output\": \" -4.402\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Propyne\\n\",\n        \"output\": \" CC#C\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 3-Chlorophenol\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3,5-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring2][Ring1][Ring1][Ring1][#Branch2]\\n\",\n        \"output\": \" -7.02\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Methylcyclohexane \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Octyne \\n\",\n        \"output\": \" [C][C][C][C][C][C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Hexyne \\n\",\n        \"output\": \" [C][C][C][C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl nonanoate\\n\",\n        \"output\": \" InChI=1S/C11H22O2/c1-3-5-6-7-8-9-10-11(12)13-4-2/h3-10H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Chlorobiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Bensulide\\n\",\n        \"output\": \" [C][C][Branch1][C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][O][C][Branch1][C][C][C][S][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" m-Chlorobromobenzene\\n\",\n        \"output\": \" -3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCOc1ccc(cc1)C(C)(C)COCc3cccc(Oc2ccccc2)c3\\n\",\n        \"output\": \" 2.511886431509582e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0006456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fluorobenzene\\n\",\n        \"output\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" N,N-Diethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H2\\n\",\n        \"output\": \" p-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][O]\\n\",\n        \"output\": \" 5.011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2\\n\",\n        \"output\": \" Fluorene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -4.56\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9)\\n\",\n        \"output\": \" Flucytosine\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 2,4,6-Trimethylphenol\\n\",\n        \"output\": \" 0.008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=O]\\n\",\n        \"output\": \" Acrolein\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Diphenylamine\\n\",\n        \"output\": \" 0.0003133285724315589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Triazolam\\n\",\n        \"output\": \" [C][C][=N][N][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" cis-1,2-Dimethylcyclohexane\\n\",\n        \"output\": \" InChI=1S/C8H16/c1-7-5-3-4-6-8(7)2/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H9NO/c1-4(6)5(2)3/h1-3H3\\n\",\n        \"output\": \" N,N-Dimethylacetamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][O][C][Ring1][Branch1]\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethalfluralin\\n\",\n        \"output\": \" CCN(CC(C)=C)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10Cl12/c11-1-2(12)7(17)4(14)3(13,5(1,15)9(7,19)20)6(1,16)10(21,22)8(2,4)18\\n\",\n        \"output\": \" -6.8\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 4-Bromotoluene\\n\",\n        \"output\": \" Cc1ccc(Br)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H\\n\",\n        \"output\": \" Benzene \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H5N3O/c6-5(9)4-3-7-1-2-8-4/h1-3H,(H2,6,9)\\n\",\n        \"output\": \" 0.21527817347243727 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-15,18,22,26H,3-8,10-11H2,1-2H3\\n\",\n        \"output\": \" 0.0007762471166286919 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Octanol\\n\",\n        \"output\": \" CCCCCC(O)CC\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" trans-2-Heptene \\n\",\n        \"output\": \" InChI=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" -3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC12CCC(O)CC1CCC3C2CCC4(C)C3CCC4=O\\n\",\n        \"output\": \" -4.402\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,2,3,5-Tetrachlorobenzene\\n\",\n        \"output\": \" -4.63\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Methyl-3-pentanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Iodopropane\\n\",\n        \"output\": \" CCCI\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H16O2/c1-3-5-6-7-10-8(9)4-2/h3-7H2,1-2H3\\n\",\n        \"output\": \" Ethyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" m-Xylene \\n\",\n        \"output\": \" InChI=1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C4H4O/c1-2-4-5-3-1/h1-4H\\n\",\n        \"output\": \" 0.15135612484362082 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCC=C\\n\",\n        \"output\": \" -3.73\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3-Methylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCCC\\n\",\n        \"output\": \" -4.53\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Anisole\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" ClC(Cl)(Cl)C#N\\n\",\n        \"output\": \" 0.0067920363261718434 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H22O2/c1-3-5-6-7-8-9-10-11(12)13-4-2/h3-10H2,1-2H3\\n\",\n        \"output\": \" 0.00015848931924611142 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" N-Ethylaniline\\n\",\n        \"output\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H2ClN/c3-1-2-4/h1H2\\n\",\n        \"output\": \" Chloroacetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H\\n\",\n        \"output\": \" 2,6-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.0003715352290971724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ioxynil\\n\",\n        \"output\": \" InChI=1S/C7H3I2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)SC(C)C\\n\",\n        \"output\": \" Diisopropylsulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" C=CCC=C\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3\\n\",\n        \"output\": \" Methazole\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,3-Dimethylnaphthalene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSCC\\n\",\n        \"output\": \" -4.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][C][=C]\\n\",\n        \"output\": \" 1,4-Pentadiene \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -3.094\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" hematein\\n\",\n        \"output\": \" [C][=C][C][Branch1][C][O][=C][Branch1][C][O][C][O][C][C][Branch1][C][O][C][C][=C][C][=Branch1][C][=O][C][Branch1][C][O][=C][C][Ring1][Branch2][=C][Ring1][N][C][=Ring1][S][Ring2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Procymidone\\n\",\n        \"output\": \" [C][C][C][C][Ring1][Ring1][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][Branch2][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCC=C\\n\",\n        \"output\": \" 1-Hexene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Diphenylamine\\n\",\n        \"output\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][S][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.24\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-5-6-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" 0.21877616239495523 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanol\\n\",\n        \"output\": \" CC(O)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Dimecron\\n\",\n        \"output\": \" 0.523\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyclohexanone\\n\",\n        \"output\": \" InChI=1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)\\n\",\n        \"output\": \" 1.9952623149688795 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-2-4(8)6(10)5(3)9/h1-2,10H\\n\",\n        \"output\": \" 2,3,6-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H19N3O5S2/c1-8-10(12(19)16-13(20)14-8)3-4-11(18)15-9(5-17)6-23(21)7-22-2/h3-4,9,17H,5-7H2,1-2H3,(H,15,18)(H2,14,16,19,20)\\n\",\n        \"output\": \" Sparsomycin (3,8mg/ml)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Methyl-3-hexanol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Metolcarb\\n\",\n        \"output\": \" InChI=1S/C8H9NO2/c1-9-8(10)11-7-5-3-2-4-6-7/h2-6H,1H3,(H,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)c1ccccc1\\n\",\n        \"output\": \" N,N-Dimethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" norethindrone acetate\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCOC(=O)CC\\n\",\n        \"output\": \" Methyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" p-Nitroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCOC(=O)CC\\n\",\n        \"output\": \" -1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][I][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H18O2/c1-3-4-5-6-7-8-9(10)11-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" Methyl octanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][C][C][C][C]\\n\",\n        \"output\": \" 7.177942912713615e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCC(=C)C\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H19ClNO3PS2/c1-10(2)15(12-7-5-11(14)6-8-12)13(16)9-21-19(20,17-3)18-4/h5-8,10H,9H2,1-4H3\\n\",\n        \"output\": \" Anilofos\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Epiandrosterone\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Clc1ccccc1\\n\",\n        \"output\": \" -2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chloroethylene\\n\",\n        \"output\": \" ClC=C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\\n\",\n        \"output\": \" 4.5708818961487516e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1NCCN1c2ncc(s2)N(=O)=O\\n\",\n        \"output\": \" Niridazole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C]\\n\",\n        \"output\": \" Pentane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCl\\n\",\n        \"output\": \" 1-Chloroheptane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" -4.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H6N4O/c1-12-7-10-4-5-6(11-7)9-3-2-8-5/h2-4H,1H3\\n\",\n        \"output\": \" 2-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" -0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Ethylhexanal\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CN(C)c1nc(nc(n1)N(C)C)N(C)C\\n\",\n        \"output\": \" -3.364\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C/C1CCCCC1\\\\C\\n\",\n        \"output\": \" cis-1,2-Dimethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C18H20O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3-5,10,14,16,19H,2,6-9H2,1H3\\n\",\n        \"output\": \" -5.282\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CC=C(C)C\\n\",\n        \"output\": \" 5-(3-Methyl-2-butenyl)-5-ethylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Tricresyl phosphate\\n\",\n        \"output\": \" -6.01\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Hexanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" o-Methoxyphenol\\n\",\n        \"output\": \" InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" o-Hydroxybenzamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][=O]\\n\",\n        \"output\": \" D-fenchone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2HCl3/c3-1-2(4)5/h1H\\n\",\n        \"output\": \" Trichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C24H32O4S/c1-14(25)29-19-13-15-12-16(26)4-8-22(15,2)17-5-9-23(3)18(21(17)19)6-10-24(23)11-7-20(27)28-24/h12,17-19,21H,4-11,13H2,1-3H3\\n\",\n        \"output\": \" -4.173\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccncc1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Glafenine\\n\",\n        \"output\": \" 2.6853444456585036e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccncc1C\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethyl pentanoate\\n\",\n        \"output\": \" CCCOC(=O)CCC\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCC(C)O\\n\",\n        \"output\": \" -0.89\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cyclopentane \\n\",\n        \"output\": \" [C][C][C][C][C][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][O][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" 3-Ethyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H8/c1-4(2)3/h1H2,2-3H3\\n\",\n        \"output\": \" 2-Methylpropene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1ccccc1N(=O)=O\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Salicylamide\\n\",\n        \"output\": \" -1.8359999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Lenacil\\n\",\n        \"output\": \" O=c2[nH]c1CCCc1c(=O)n2C3CCCCC3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pentylbenzene\\n\",\n        \"output\": \" [C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Br][Br][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" 3.962780342554385e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Butethal\\n\",\n        \"output\": \" 0.021827299118430014 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pentachlorobenzene\\n\",\n        \"output\": \" Clc1cc(Cl)c(Cl)c(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methylphenol\\n\",\n        \"output\": \" Cc1ccccc1O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1,4-Benzenediol\\n\",\n        \"output\": \" 0.6760829753919817 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,4-Dimethyl-3-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Clc1cccc(c1Cl)c2cccc(Cl)c2Cl\\n\",\n        \"output\": \" 5.248074602497723e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCOc1ccc(NC(=O)C)cc1\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CNC(=O)Oc1ccc(N(C)C)c(C)c1\\n\",\n        \"output\": \" Aminocarb\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Indole\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" P,P'-DDE\\n\",\n        \"output\": \" InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H18O2/c1-3-5-6-7-8-9(10)11-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" Ethyl heptanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C26H54/c1-3-5-7-9-11-13-15-17-19-21-23-25-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-26H2,1-2H3\\n\",\n        \"output\": \" 4.634469197362884e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H3Cl3/c7-4-2-1-3-5(8)6(4)9/h1-3H\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C15H23N3O4/c1-5-7-16(8-6-2)15-13(17(19)20)9-12(11(3)4)10-14(15)18(21)22/h9-11H,5-8H2,1-4H3\\n\",\n        \"output\": \" Isopropalin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Propoxur\\n\",\n        \"output\": \" InChI=1S/C11H15NO3/c1-8(2)14-9-6-4-5-7-10(9)15-11(13)12-3/h4-8H,1-3H3,(H,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][Br]\\n\",\n        \"output\": \" -0.89\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Furane\\n\",\n        \"output\": \" [C][C][=C][O][C][=Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" p-Methoxybenzaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Nonanone\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H15O3PS2/c1-8-7-9(5-6-10(8)16-4)13-14(15,11-2)12-3/h5-7H,1-4H3\\n\",\n        \"output\": \" Fenthion\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Propoxur\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Br][C][C][Br]\\n\",\n        \"output\": \" 1,2-Dibromoethane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" NC(=S)Nc1ccccc1\\n\",\n        \"output\": \" 0.016982436524617443 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,1,1,2-Tetrachloroethane\\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" OCC1OC(CO)(OC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)C(O)C1O\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-hydroxypteridine\\n\",\n        \"output\": \" 0.011297959146727982 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3-Methylbutan-1-ol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-5(2)3-4-6/h5-6H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.000328851630875983 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Cortisone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccc(OP(=O)(Oc2cccc(C)c2)Oc3ccccc3C)cc1\\n\",\n        \"output\": \" 9.77237220955811e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Ethyl formate\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-Ethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C]\\n\",\n        \"output\": \" Hydroxyprogesterone-17a\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][S][C][=Ring1][Branch1]\\n\",\n        \"output\": \" Thiophene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 3,5-Dimethylphenol\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3,5-8H,1,4H2,2H3\\n\",\n        \"output\": \" -2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCl\\n\",\n        \"output\": \" 0.033884415613920256 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Nitromethane\\n\",\n        \"output\": \" [C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C16H12O6/c17-10-2-1-8-13-9-4-12(19)11(18)3-7(9)5-16(13,21)6-22-15(8)14(10)20/h1-4,17,19-21H,5-6H2\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" Trifluralin\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC34CC(O)C1(F)C(CCC2=CC(=O)C=CC12C)C3CC(O)C4(O)C(=O)CO\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Ditalimfos\\n\",\n        \"output\": \" -3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" ClC(Cl)(Cl)N(=O)=O\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H\\n\",\n        \"output\": \" Phenol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-7,11H,1-3H3\\n\",\n        \"output\": \" 0.006025595860743574 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" C1CC=CC1\\n\",\n        \"output\": \" 0.007943282347242814 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-14-8-4-2-6-12(14)10-13-7-3-5-9-15(11)13/h2-10H,1H3\\n\",\n        \"output\": \" 9-Methylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.18197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H21N2O3PS/c1-6-15-18(19,16-7-2)17-11-8-10(5)13-12(14-11)9(3)4/h8-9H,6-7H2,1-5H3\\n\",\n        \"output\": \" 0.00022908676527677723 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCC2NC(=O)c1cc(c(Cl)cc1N2)S(N)(=O)=O\\n\",\n        \"output\": \" 0.0005128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Chloro-2-methylbutane\\n\",\n        \"output\": \" InChI=1S/C5H11Cl/c1-4-5(2,3)6/h4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Diuron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc(cc1)c2ccc(cc2)c3ccccc3\\n\",\n        \"output\": \" p-terphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2,4,5-Tetrachlorobenzene\\n\",\n        \"output\": \" Clc1cc(Cl)c(Cl)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H4BrF/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" -2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][C][N][Ring1][Branch1][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Niridazole\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Clc1cc(Cl)cc(Cl)c1\\n\",\n        \"output\": \" -4.48\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,8-Cineole\\n\",\n        \"output\": \" InChI=1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Eriodictyol\\n\",\n        \"output\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Isoproturon\\n\",\n        \"output\": \" -3.536\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)\\n\",\n        \"output\": \" Theophylline\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch2][Ring1][=C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring2][Ring1][Ring1][Ring1][#C][Cl]\\n\",\n        \"output\": \" Mirex\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)\\n\",\n        \"output\": \" -2.6919999999999997\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 5,5-Diallylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][=Branch1][Ring1][=C][Cl][Cl]\\n\",\n        \"output\": \" -4.2860000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.00353183169791957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H6N4/c1-5-6-7(11-4-10-5)9-3-2-8-6/h2-4H,1H3\\n\",\n        \"output\": \" 0.3419794425137088 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benzo(e)pyrene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][=Branch1][=C][Ring1][#Branch2][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][I]\\n\",\n        \"output\": \" 1-Iodoheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" methyl laurate\\n\",\n        \"output\": \" InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CN(C(=O)COc1nc2ccccc2s1)c3ccccc3\\n\",\n        \"output\": \" -4.873\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Dicapthon\\n\",\n        \"output\": \" InChI=1S/C8H9ClNO5PS/c1-13-16(17,14-2)15-8-4-3-6(10(11)12)5-7(8)9/h3-5H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 3-Methyl-3-heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-8(2)9-6-4-3-5-7-9/h3-8H,1-2H3\\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccccc1Br\\n\",\n        \"output\": \" 2-Bromotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCCO\\n\",\n        \"output\": \" 1-Nonanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2,3-Dichloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Bromooctane\\n\",\n        \"output\": \" -5.06\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Hexestrol\\n\",\n        \"output\": \" InChI=1S/C18H22O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,17-20H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc2ncc1nccnc1n2\\n\",\n        \"output\": \" 2-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Heptanol \\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Cc1cc(ccc1NS(=O)(=O)C(F)(F)F)S(=O)(=O)c2ccccc2\\n\",\n        \"output\": \" 0.00015848931924611142 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 2.0892961308540407e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 1-Butanol\\n\",\n        \"output\": \" 1.0 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benzo(j)fluoranthene\\n\",\n        \"output\": \" InChI=1S/C20H12/c1-2-8-15-13(5-1)11-12-17-16-9-3-6-14-7-4-10-18(19(14)16)20(15)17/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][Branch1][Ring1][O][C][=C][C][=C][Branch1][Ring2][C][C][=C][C][=C][Ring1][O]\\n\",\n        \"output\": \" 0.001202264434617413 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" typhoon\\n\",\n        \"output\": \" typhoon does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCC(CC)CO\\n\",\n        \"output\": \" 2-Ethyl-1-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 2-Chlorotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-3-5-4-2/h3H,1,4H2,2H3\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 3-Methylpentane\\n\",\n        \"output\": \" -3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" C1CCOCC1\\n\",\n        \"output\": \" -0.03\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 2.0892961308540407e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10Cl10O/c11-2-1(21)3(12)6(15)4(2,13)8(17)5(2,14)7(3,16)9(6,18)10(8,19)20\\n\",\n        \"output\": \" Kepone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C]\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 3-Methyl-2-butanone\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,6-Dichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Methylphenanthrene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][=N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2][=C][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-2-3-4-7-5-6/h5H,2-4H2,1H3\\n\",\n        \"output\": \" Butyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Pentylcyclopentane\\n\",\n        \"output\": \" -6.08\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Chloroanisole\\n\",\n        \"output\": \" COc1cccc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Dipropyl ether\\n\",\n        \"output\": \" 0.023988329190194897 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C]\\n\",\n        \"output\": \" 0.01148153621496883 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" linalool\\n\",\n        \"output\": \" CC(C)=CCCC(O)(C)C=C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch2][Ring1][O][O][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C]\\n\",\n        \"output\": \" 1.188502227437019e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][C][Ring1][#C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Methylheptane\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H\\n\",\n        \"output\": \" Anthraquinone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,4,6-Trimethylphenol\\n\",\n        \"output\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3\\n\",\n        \"output\": \" 1-Chlorobutane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14S/c1-3-5-7-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" Di-n-propylsulfide\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Dicapthon\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Metronidazole\\n\",\n        \"output\": \" Cc1ncc(N(=O)=O)n1CCO\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Nonene \\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][Branch1][C][N][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=N][C]\\n\",\n        \"output\": \" 0.23768402866248767 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H18O3/c1-8-10-4-6-15(3)7-5-11(16)9(2)12(15)13(10)18-14(8)17/h5,7-8,10,13H,4,6H2,1-3H3\\n\",\n        \"output\": \" Santonin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Iodobutane\\n\",\n        \"output\": \" InChI=1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pentamethylbenzene\\n\",\n        \"output\": \" InChI=1S/C11H16/c1-7-6-8(2)10(4)11(5)9(7)3/h6H,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H18N2O/c1-9(2)10-5-7-11(8-6-10)13-12(15)14(3)4/h5-9H,1-4H3,(H,13,15)\\n\",\n        \"output\": \" Isoproturon\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][N][C]\\n\",\n        \"output\": \" 0.01573982864466219 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its oil solubility expressed as a logarithm in mol/L. ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Isazofos\\n\",\n        \"output\": \" InChI=1S/C9H17ClN3O3PS/c1-5-14-17(18,15-6-2)16-9-11-8(10)13(12-9)7(3)4/h7H,5-6H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benzylchloride\\n\",\n        \"output\": \" [Cl][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C17H12Cl2N4/c1-10-21-22-16-9-20-17(12-4-2-3-5-14(12)19)13-8-11(18)6-7-15(13)23(10)16/h2-8H,9H2,1H3\\n\",\n        \"output\": \" 8.128305161640995e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CN2C(=O)CN=C(c1ccccc1)c3cc(Cl)ccc23\\n\",\n        \"output\": \" Diazepam\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methyl butyrate\\n\",\n        \"output\": \" [C][C][C][O][C][=Branch1][C][=O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlorotoluron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1ccc(C)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H30/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3-14H2,1-2H3\\n\",\n        \"output\": \" 1.0964781961431851e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" allicin\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][NH1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=Branch1][C][=O][C][=Ring1][Branch2][Cl][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Terbacil\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Bromodichloromethane\\n\",\n        \"output\": \" [Br][C][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" hexacosane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Permethrin\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCSP(=O)(SCCCC)SCCCC\\n\",\n        \"output\": \" 7.244359600749906e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" C1OC(O)C(O)C(O)C1O\\n\",\n        \"output\": \" 2.4547089156850306 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" 2-Bromotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 3,3-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" N-Ethylaniline\\n\",\n        \"output\": \" InChI=1S/C8H11N/c1-2-9-8-6-4-3-5-7-8/h3-7,9H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC(C)CCOC(=O)C\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H14/c1-7-5-3-2-4-6-7/h7H,2-6H2,1H3\\n\",\n        \"output\": \" Methylcyclohexane \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1ccc2c(c1)ccc3c2ccc4c5ccccc5ccc43\\n\",\n        \"output\": \" Picene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][#C]\\n\",\n        \"output\": \" 1-Pentyne\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Quinonamid\\n\",\n        \"output\": \" InChI=1S/C13H8Cl3NO3/c14-8(15)5-9(18)17-11-10(16)12(19)6-3-1-2-4-7(6)13(11)20/h1-4,8H,5H2,(H,17,18)\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Trifluralin\\n\",\n        \"output\": \" InChI=1S/C13H16F3N3O4/c1-3-5-17(6-4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccccc1\\n\",\n        \"output\": \" -2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H30OS/c1-18-8-7-14-12(13(18)5-6-17(18)20)4-3-11-9-15-16(21-15)10-19(11,14)2/h11-17,20H,3-10H2,1-2H3\\n\",\n        \"output\": \" Epitostanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 7.079457843841373e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CSc1nnc(c(=O)n1N)C(C)(C)C\\n\",\n        \"output\": \" 0.005584701947368306 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O\\n\",\n        \"output\": \" Lactose\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" C1c2ccccc2c3ccccc13\\n\",\n        \"output\": \" -5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][Branch2][O][C][=Branch1][C][=O][N][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" -4.24\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\\n\",\n        \"output\": \" Epiandrosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCSP(=O)(SCCCC)SCCCC\\n\",\n        \"output\": \" DEF\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Benzylchloride\\n\",\n        \"output\": \" InChI=1S/C7H7Cl/c8-6-7-4-2-1-3-5-7/h1-5H,6H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" C1Cc2ccccc2C1\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(Cl)CCl\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Ring2][C][=C][C][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" -3.13\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Butabarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)CC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dimefuron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][S][=C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" -5.282\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Methyl hydrazine\\n\",\n        \"output\": \" InChI=1S/CH6N2/c1-3-2/h3H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1c2ccccc2c3cc4ccccc4cc13\\n\",\n        \"output\": \" Benzo(b)fluorene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)I\\n\",\n        \"output\": \" 2-Iodopropane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C24H38O4/c1-19(2)13-7-5-11-17-27-23(25)21-15-9-10-16-22(21)24(26)28-18-12-6-8-14-20(3)4/h9-10,15-16,19-20H,5-8,11-14,17-18H2,1-4H3\\n\",\n        \"output\": \" -6.6370000000000005\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=N][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][N][Ring1][Branch2][C][C][O]\\n\",\n        \"output\": \" -1.22\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-methylpteridine\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" ClC(=C(Cl)C(=C(Cl)Cl)Cl)Cl\\n\",\n        \"output\": \" -4.92\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" Toluene \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" DDE\\n\",\n        \"output\": \" -6.9\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" 1,2-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][Branch1][C][O][=C][Branch1][C][C][C][=C][C][Branch1][=Branch1][C][Branch1][C][C][C][=C][Ring1][O]\\n\",\n        \"output\": \" 0.008317637711026709 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccccc1C\\n\",\n        \"output\": \" 0.001584893192461114 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Phenylphenol\\n\",\n        \"output\": \" InChI=1S/C12H10O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,13H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Bromoethane\\n\",\n        \"output\": \" -1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,4-Dinitrotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methyltetrahydrofurane\\n\",\n        \"output\": \" [C][C][C][C][C][O][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)\\n\",\n        \"output\": \" Formetanate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)OC=O\\n\",\n        \"output\": \" Isopropyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Carboxin\\n\",\n        \"output\": \" -3.14\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H15NO3/c1-12(2)7-8-5-4-6-9(10(8)16-12)15-11(14)13-3/h4-6H,7H2,1-3H3,(H,13,14)\\n\",\n        \"output\": \" Carbofuran\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=O]\\n\",\n        \"output\": \" Formothion\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.0025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H4O2/c1-4-2-3/h2H,1H3\\n\",\n        \"output\": \" Methyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Pentanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Dodecanol\\n\",\n        \"output\": \" InChI=1S/C12H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-12H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Disulfiram\\n\",\n        \"output\": \" -4.86\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H8/c1-2-4-5-3-1/h1-2H,3-5H2\\n\",\n        \"output\": \" Cyclopentene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dienochlor\\n\",\n        \"output\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][=Branch2][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][C][Branch1][C][Cl][C][=Branch1][=N][=C][Branch1][C][Cl][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=C]\\n\",\n        \"output\": \" Ethyl vinyl ether\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H9Cl2NO3/c1-3-12(2)10(16)15(11(17)18-12)9-5-7(13)4-8(14)6-9/h3-6H,1H2,2H3\\n\",\n        \"output\": \" -4.925\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Butylbenzene\\n\",\n        \"output\": \" CCCCc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][=Branch2]\\n\",\n        \"output\": \" 6.025595860743581e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)SC(CCl)N1C(=O)c2ccccc2C1=O\\n\",\n        \"output\": \" Dialifor\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC(=O)C\\n\",\n        \"output\": \" 0.9120108393559098 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Diazinon\\n\",\n        \"output\": \" -3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H3Br3/c7-4-1-5(8)3-6(9)2-4/h1-3H\\n\",\n        \"output\": \" 2.5118864315095823e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H18N2O2/c16-12-10-7-4-8-11(10)14-13(17)15(12)9-5-2-1-3-6-9/h9H,1-8H2,(H,14,17)\\n\",\n        \"output\": \" Lenacil\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(C)c(Cl)c1\\n\",\n        \"output\": \" -3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Acenapthene\\n\",\n        \"output\": \" C1Cc2cccc3cccc1c23\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 2,3,5-Trichlorophenol\\n\",\n        \"output\": \" 0.0021379620895022326 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 0.19498445997580455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC23Cc1cnoc1C=C2CCC4C3CCC5(C)C4CCC5(O)C#C\\n\",\n        \"output\": \" 3.1117163371060134e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N]\\n\",\n        \"output\": \" 0.006165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" t-Crotonaldehyde\\n\",\n        \"output\": \" C/C=C/C=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2',3,4,5,5'-PCB\\n\",\n        \"output\": \" Clc1ccc(Cl)c(c1)c2cc(Cl)c(Cl)c(Cl)c2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Inosine\\n\",\n        \"output\": \" InChI=1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" alloxantin\\n\",\n        \"output\": \" [C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][=Branch2][Branch1][C][O][C][Branch1][C][O][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility expressed as a logarithm in mol/L of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H21O2PS3/c1-6-10-12(13,11-7-2)15-8-14-9(3,4)5/h6-8H2,1-5H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" 0.0009120108393559096 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCOC(=O)C\\n\",\n        \"output\": \" 0.012882495516931342 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCCCC#C\\n\",\n        \"output\": \" 5.7543993733715664e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Bromomethane\\n\",\n        \"output\": \" CBr\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1=C(SCCO1)C(=O)Nc2ccccc2\\n\",\n        \"output\": \" Carboxin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Chloropropane\\n\",\n        \"output\": \" CC(C)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][=Branch1][Ring1][=C][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" Stirofos\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4N2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H\\n\",\n        \"output\": \" 1,4-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pentyl acetate\\n\",\n        \"output\": \" InChI=1S/C7H14O2/c1-3-4-5-6-9-7(2)8/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Phenylmethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H3\\n\",\n        \"output\": \" -4.24\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)\\n\",\n        \"output\": \" 0.10351421666793438 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlorbromuron\\n\",\n        \"output\": \" CON(C)C(=O)Nc1ccc(Br)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(C)CO\\n\",\n        \"output\": \" 2-Methylbutanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Nonane\\n\",\n        \"output\": \" -5.88\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c2ccc1[nH]ccc1c2\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Mefluidide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N][C][=C][C][Branch1][P][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][=C][Branch1][C][C][C][=C][Ring1][#C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C19H23N3/c1-14-6-8-18(16(3)10-14)20-12-22(5)13-21-19-9-7-15(2)11-17(19)4/h6-13H,1-5H3\\n\",\n        \"output\": \" 3.3884415613920275e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C]\\n\",\n        \"output\": \" 0.0001445439770745928 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Isonazid\\n\",\n        \"output\": \" 1.02093948370768 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C][Branch1][N][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccsc1\\n\",\n        \"output\": \" Thiophene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring1][C][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" Trichloronate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,2,4,5-Tetrabromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H2Br4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCC(C)Cl\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Mefenacet\\n\",\n        \"output\": \" CN(C(=O)COc1nc2ccccc2s1)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethanethiol\\n\",\n        \"output\": \" InChI=1S/C2H6S/c1-2-3/h3H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3\\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Hexadecane\\n\",\n        \"output\": \" CCCCCCCCCCCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dialifor\\n\",\n        \"output\": \" CCOP(=S)(OCC)SC(CCl)N1C(=O)c2ccccc2C1=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H16N2O3/c1-3-13-11(15)9(2)17-12(16)14-10-7-5-4-6-8-10/h4-9H,3H2,1-2H3,(H,13,15)(H,14,16)\\n\",\n        \"output\": \" Carbetamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" 0.30902954325135906 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][#C]\\n\",\n        \"output\": \" 0.057543993733715694 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its solubility in room temperature. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Deoxycorticosterone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Fluorometuron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1cccc(c1)C(F)(F)F\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Acenapthylene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 9,10-Dimethylanthracene\\n\",\n        \"output\": \" InChI=1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.00035399734108343465 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Benzoxazole\\n\",\n        \"output\": \" -1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,3',4',5-PCB\\n\",\n        \"output\": \" Clc1ccc(Cl)c(c1)c2ccc(Cl)c(Cl)c2\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chlorotoluron\\n\",\n        \"output\": \" InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-5-6(2,3)4/h5H2,1-4H3\\n\",\n        \"output\": \" 0.0002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C]\\n\",\n        \"output\": \" 17a-Methyltestosterone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 1,1,2,2-Tetrachloroethane\\n\",\n        \"output\": \" 0.018197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC(Cl)(Cl)C#N\\n\",\n        \"output\": \" Trichloroacetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2,3,4-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -6.89\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methylpropane\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methyl-3-pentanol\\n\",\n        \"output\": \" CCC(O)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Carbophenthion\\n\",\n        \"output\": \" InChI=1S/C11H16ClO2PS3/c1-3-13-15(16,14-4-2)18-9-17-11-7-5-10(12)6-8-11/h5-8H,3-4,9H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Theophylline\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][NH1][C][=Ring1][Branch1][C][Ring1][O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 2,3-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)C(=O)C\\n\",\n        \"output\": \" 3-Methyl-2-butanone\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][#N]\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2Cl2F4/c3-1(5,6)2(4,7)8\\n\",\n        \"output\": \" -2.74\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" cis-1,2-Dimethylcyclohexane\\n\",\n        \"output\": \" [C][/C][C][C][C][C][C][Ring1][=Branch1][\\\\C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" DEF\\n\",\n        \"output\": \" -5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" m-Chlorobromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4BrCl/c7-5-2-1-3-6(8)4-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14S/c1-5(2)7-6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" -2.24\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)COC=O\\n\",\n        \"output\": \" 0.09772372209558107 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propiconazole\\n\",\n        \"output\": \" InChI=1S/C15H17Cl2N3O2/c1-2-3-12-7-21-15(22-12,8-20-10-18-9-19-20)13-5-4-11(16)6-14(13)17/h4-6,9-10,12H,2-3,7-8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Cresol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Aniline \\n\",\n        \"output\": \" 0.3890451449942806 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C21H16/c1-13-5-8-17-15(11-13)7-9-18-19-10-6-14-3-2-4-16(21(14)19)12-20(17)18/h2-5,7-9,11-12H,6,10H2,1H3\\n\",\n        \"output\": \" -7.92\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Cyclooctanol\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" -6.726\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methyl decanoate\\n\",\n        \"output\": \" InChI=1S/C11H22O2/c1-3-4-5-6-7-8-9-10-11(12)13-2/h3-10H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCC(O)CC\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][S][C][=Branch1][C][=S][N][C][Ring1][=Branch1][=O]\\n\",\n        \"output\": \" rhodanine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Phenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCOC(C)OCC\\n\",\n        \"output\": \" 0.37153522909717257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCOP(=S)(OCC)SC(CCl)N1C(=O)c2ccccc2C1=O\\n\",\n        \"output\": \" 4.5708818961487516e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Cc1cccc(C)c1O\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Diphenylmethane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Propyl butyrate\\n\",\n        \"output\": \" 0.012022644346174132 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" DNOC\\n\",\n        \"output\": \" Cc1cc(cc(N(=O)=O)c1O)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Br]\\n\",\n        \"output\": \" 2-Bromopropane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H\\n\",\n        \"output\": \" 2,4,6-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" Benzyltrifluoride\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" o-Nitroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COC1=CC(=O)CC(C)C13Oc2c(Cl)c(OC)cc(OC)c2C3=O\\n\",\n        \"output\": \" Griseofulvin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Ic1ccccc1\\n\",\n        \"output\": \" Iodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" 2-Methylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\\n\",\n        \"output\": \" Androsterone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC34CCC1C(=CCc2cc(O)ccc12)C3CCC4=O\\n\",\n        \"output\": \" Equilin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCNc1nc(Cl)nc(NC(C)(C)C#N)n1\\n\",\n        \"output\": \" -3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-6(2,3)4-5-7/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.31622776601683794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Cl]\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC#C\\n\",\n        \"output\": \" Propyne\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Estrone\\n\",\n        \"output\": \" InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Br]\\n\",\n        \"output\": \" 1-Bromopropane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 1,3-Dibromobenzene\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCC(C)C\\n\",\n        \"output\": \" 8.31763771102671e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Propyl acetate\\n\",\n        \"output\": \" [C][C][C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Chlorobiphenyl\\n\",\n        \"output\": \" InChI=1S/C12H9Cl/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H18N2O2/c16-12-10-7-4-8-11(10)14-13(17)15(12)9-5-2-1-3-6-9/h9H,1-8H2,(H,14,17)\\n\",\n        \"output\": \" 2.5468302525850444e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Diazinon\\n\",\n        \"output\": \" InChI=1S/C12H21N2O3PS/c1-6-15-18(19,16-7-2)17-11-8-10(5)13-12(14-11)9(3)4/h8-9H,6-7H2,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H9Cl2NO2/c12-6-1-2-7-16-11(15)14-10-5-3-4-9(13)8-10/h3-5,8H,6-7H2,(H,14,15)\\n\",\n        \"output\": \" 4.265795188015926e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H8N2O3/c10-4-7(2-1-3-7)5(11)9-6(12)8-4/h1-3H2,(H2,8,9,10,11,12)\\n\",\n        \"output\": \" Cyclobutyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Etoposide (148-167,25mg/ml)\\n\",\n        \"output\": \" InChI=1S/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Pyrazon\\n\",\n        \"output\": \" Nc2cnn(c1ccccc1)c(=O)c2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H20O2/c1-3-5-6-7-8-9-10(11)12-4-2/h3-9H2,1-2H3\\n\",\n        \"output\": \" Ethyl octanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1cc2ccc3ccc4ccc5cccc6c(c1)c2c3c4c56\\n\",\n        \"output\": \" Benzo[ghi]perylene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCNc1nc(Cl)nc(NC(C)C)n1\\n\",\n        \"output\": \" Atrazine\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2,4-Trichlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3Cl3/c7-4-1-2-5(8)6(9)3-4/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,2',3,4,5,5'-PCB\\n\",\n        \"output\": \" InChI=1S/C12H4Cl6/c13-5-1-2-8(14)6(3-5)7-4-9(15)11(17)12(18)10(7)16/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H8/c1-2-4-6-5-3-1/h1-2,5-6H,3-4H2\\n\",\n        \"output\": \" 1,4-Cyclohexadiene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 3-Heptanol \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H15Cl3O2/c1-20-13-7-3-11(4-8-13)15(16(17,18)19)12-5-9-14(21-2)10-6-12/h3-10,15H,1-2H3\\n\",\n        \"output\": \" -6.89\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Anilofos\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,3,5-Trichlorophenol\\n\",\n        \"output\": \" Oc1cc(Cl)cc(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Propyl formate\\n\",\n        \"output\": \" [C][C][C][O][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC(C)C\\n\",\n        \"output\": \" 2-Methylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Tetrafluthrin\\n\",\n        \"output\": \" -7.321000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCC(=O)OC\\n\",\n        \"output\": \" 0.0006760829753919819 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Ethyl propyl ether\\n\",\n        \"output\": \" 0.21877616239495523 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H14N2O3/c1-4-5-10(6(2)3)7(13)11-9(15)12-8(10)14/h4,6H,1,5H2,2-3H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 5-Allyl-5-isopropylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Nitropropane\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C(C)C(C)C\\n\",\n        \"output\": \" 2,3,4-Trimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Isopropylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C24H38O4/c1-5-9-13-19(7-3)17-27-23(25)21-15-11-12-16-22(21)24(26)28-18-20(8-4)14-10-6-2/h11-12,15-16,19-20H,5-10,13-14,17-18H2,1-4H3\\n\",\n        \"output\": \" -6.96\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Trichloronate\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring1][C][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Carbaryl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-5-6-7-8(9)4-2/h8-9H,3-7H2,1-2H3\\n\",\n        \"output\": \" 3-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C26H23F2NO4/c1-17(2)24(18-11-13-21(14-12-18)32-26(27)28)25(30)33-23(16-29)19-7-6-10-22(15-19)31-20-8-4-3-5-9-20/h3-15,17,23-24,26H,1-2H3\\n\",\n        \"output\": \" 1.33045441797809e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" oryzalin\\n\",\n        \"output\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][S][Branch1][C][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][#C]\\n\",\n        \"output\": \" 1-Heptyne\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Chloroanisole\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" DNOC\\n\",\n        \"output\": \" InChI=1S/C7H6N2O5/c1-4-2-5(8(11)12)3-6(7(4)10)9(13)14/h2-3,10H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dipropyl ether\\n\",\n        \"output\": \" [C][C][C][O][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCN(CC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" Benfluralin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][Branch1][#Branch1][C][C][Branch1][C][C][=C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -6.124\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(O)CC\\n\",\n        \"output\": \" 0.5754399373371569 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Methoprene\\n\",\n        \"output\": \" 6.456542290346549e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 2,4-Dichlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][O][C][C][O]\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Carbazole\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H8O/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\\n\",\n        \"output\": \" Dibenzofurane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Acenapthylene\\n\",\n        \"output\": \" InChI=1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ccc(O)cc1\\n\",\n        \"output\": \" p-Cresol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3\\n\",\n        \"output\": \" 2,6-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H12N2O3/c1-3-5-10(6-4-2)7(13)11-9(15)12-8(10)14/h3-4H,1-2,5-6H2,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 0.008375292821268827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)Nc1ccccc1\\n\",\n        \"output\": \" 0.046773514128719815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" skill\\n\",\n        \"output\": \" skill does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC12CC2(C)C(=O)N(C1=O)c3cc(Cl)cc(Cl)c3\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCSCC\\n\",\n        \"output\": \" Diethyl sulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3\\n\",\n        \"output\": \" Fenitrothion\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C11H16/c1-11(2,3)9-10-7-5-4-6-8-10/h4-8H,9H2,1-3H3\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Iodobutane\\n\",\n        \"output\": \" 0.0010964781961431851 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" norethindrone acetate\\n\",\n        \"output\": \" InChI=1S/C22H28O3/c1-4-22(25-14(2)23)12-10-20-19-7-5-15-13-16(24)6-8-17(15)18(19)9-11-21(20,22)3/h1,13,17-20H,5-12H2,2-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Methyl-3-hexanol\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" cis 1,2-Dichloroethylene\\n\",\n        \"output\": \" Cl\\\\C=C/Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Chloroacetonitrile\\n\",\n        \"output\": \" -0.092\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Methyl-2-heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-7(8,5-2)6-3/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" 3-Ethyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H14N2O2S/c1-18(12-7-3-2-4-8-12)15(19)11-20-16-17-13-9-5-6-10-14(13)21-16/h2-10H,11H2,1H3\\n\",\n        \"output\": \" Mefenacet\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C21H22N2O4/c1-2-3-14-18(24)27-15-23-19(25)21(22-20(23)26,16-10-6-4-7-11-16)17-12-8-5-9-13-17/h4-13H,2-3,14-15H2,1H3,(H,22,26)\\n\",\n        \"output\": \" 3-Pentanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" vamidothion\\n\",\n        \"output\": \" CNC(=O)C(C)SCCSP(=O)(OC)(OC)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCC(=O)OCC\\n\",\n        \"output\": \" Ethyl decanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1ccc2cc3ccccc3cc2c1\\n\",\n        \"output\": \" 4.466835921509635e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1-Hexene-3-ol\\n\",\n        \"output\": \" -0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Butyl acetate\\n\",\n        \"output\": \" 0.04265795188015926 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=O)OC3(CCC4C2CCC1=CC(=O)CCC1C2CCC34C)C#C\\n\",\n        \"output\": \" norethindrone acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][N][Branch1][Ring1][C][=O][C][=N][C][Branch1][C][Cl][=C][C][Branch1][Ring1][O][C][=N][Ring1][=Branch2]\\n\",\n        \"output\": \" Chlorimuron-ethyl (ph 7)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Isoprocarb\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Estradiol\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" p-Nitroaniline\\n\",\n        \"output\": \" InChI=1S/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C#C)N(C)C(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" Buturon\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Deltamethrin\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Br][Br][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCN(CC)C(=O)SCCC\\n\",\n        \"output\": \" -3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Bromomethane\\n\",\n        \"output\": \" InChI=1S/CH3Br/c1-2/h1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC(C)C1(CC=C)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" Talbutal\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -4.74\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)\\n\",\n        \"output\": \" -2.1109999999999998\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Talbutal\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C][Branch1][Ring2][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Eugenol\\n\",\n        \"output\": \" COc1cc(CC=C)ccc1O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)CC(=O)C\\n\",\n        \"output\": \" 4-Methyl-2-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCC\\n\",\n        \"output\": \" -1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,4,5-Trichlorophenol \\n\",\n        \"output\": \" [O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CN(C=Nc1ccc(C)cc1C)C=Nc2ccc(C)cc2C\\n\",\n        \"output\": \" -5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COP(=O)(OC)OC(=CCl)c1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" Stirofos\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][C][C][C][C][Ring1][Branch2][Ring1][Branch1]\\n\",\n        \"output\": \" Norea\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2,4,6-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Chloroheptane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 5,5-Diallylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC=C)CC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(C)(C)Cl\\n\",\n        \"output\": \" -2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H7NO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" -2.41\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 4-methylpteridine\\n\",\n        \"output\": \" [C][C][=N][C][=N][C][=N][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Octadecanol\\n\",\n        \"output\": \" CCCCCCCCCCCCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H10O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,13H\\n\",\n        \"output\": \" p-Phenylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O2/c1-2-3-5-8-6-4-7/h7H,2-6H2,1H3\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,3-Benzenediol\\n\",\n        \"output\": \" InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Coronene\\n\",\n        \"output\": \" InChI=1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C]\\n\",\n        \"output\": \" 0.00015240527537972924 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" -0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCC(=O)C\\n\",\n        \"output\": \" -0.19\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc3nnc4CN=C(c1ccccc1Cl)c2cc(Cl)ccc2n34\\n\",\n        \"output\": \" -4.09\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H22O4P2S4/c1-5-10-14(16,11-6-2)18-9-19-15(17,12-7-3)13-8-4/h5-9H2,1-4H3\\n\",\n        \"output\": \" Ethion\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][I]\\n\",\n        \"output\": \" Iodoethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Fluoromethalone\\n\",\n        \"output\": \" InChI=1S/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Pentyl propanoate\\n\",\n        \"output\": \" 0.005623413251903491 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1CCCCC1\\n\",\n        \"output\": \" Cyclohexanone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CHBr2Cl/c2-1(3)4/h1H\\n\",\n        \"output\": \" Chlorodibromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl][C][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Chloramphenicol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 1-Nonene \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" C=CCS(=O)SCC=C\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc1nc(Cl)n(n1)C(C)C\\n\",\n        \"output\": \" -3.658\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cc(C)c(O)c(C)c1\\n\",\n        \"output\": \" 2,4,6-Trimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Urea\\n\",\n        \"output\": \" [N][C][=Branch1][C][=O][N]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Butyl acetate\\n\",\n        \"output\": \" [C][C][C][C][O][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-5-6-7-8(9)4-2/h8-9H,3-7H2,1-2H3\\n\",\n        \"output\": \" 0.010471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-3-5-4-2/h3H,1,4-5H2,2H3\\n\",\n        \"output\": \" 1-Pentene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-butenal\\n\",\n        \"output\": \" InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dimethoxymethane\\n\",\n        \"output\": \" [C][O][C][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" trans-2-Pentene \\n\",\n        \"output\": \" InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3+\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Metronidazole\\n\",\n        \"output\": \" -1.22\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H10O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-6H,1-2H3\\n\",\n        \"output\": \" -1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H9Cl5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H\\n\",\n        \"output\": \" Dicofol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(C)CO\\n\",\n        \"output\": \" 2-Methylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Phenacetin\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CH2Cl2/c2-1-3/h1H2\\n\",\n        \"output\": \" Dichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,3-Dimethylpyridine\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-4-3-5-8-7(6)2/h3-5H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(O)C(C)(C)C\\n\",\n        \"output\": \" 0.23988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H18NO4PS2/c1-7(8(10)9-2)15-5-6-16-14(11,12-3)13-4/h7H,5-6H2,1-4H3,(H,9,10)\\n\",\n        \"output\": \" vamidothion\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Butabarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methyl-2-pentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-4-5-6(2,3)7/h7H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][#N]\\n\",\n        \"output\": \" Acetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H14/c1-2-4-6-7-5-3-1/h1-7H2\\n\",\n        \"output\": \" -3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][I]\\n\",\n        \"output\": \" 1-Iodopropane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benzylchloride\\n\",\n        \"output\": \" ClCc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2-Butanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Acrylonitrile\\n\",\n        \"output\": \" C=CC#N\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring2][Ring1][Ring1][Ring1][#Branch2]\\n\",\n        \"output\": \" 7,12-Dimethylbenz(a)anthracene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C][C][C]\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" N,N-Dimethylacetamide\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fenpropathrin\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][Ring2][Ring1][#Branch1][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H14N2O/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19/h3-10H,1-2H3\\n\",\n        \"output\": \" Methaqualone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,3,5-Trinitrobenzene\\n\",\n        \"output\": \" O=N(=O)c1cc(cc(c1)N(=O)=O)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 5-Allyl-5-isopropylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 7-methoxypteridine\\n\",\n        \"output\": \" InChI=1S/C7H6N4O/c1-12-6-3-9-5-2-8-4-10-7(5)11-6/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" 2,2',3,4,5,5',6-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" chloropropylate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-7(8,5-2)6-3/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][=O]\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,4,6-Trinitrotoluene\\n\",\n        \"output\": \" [C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H18/c1-4-6-7-8(3)5-2/h8H,4-7H2,1-3H3\\n\",\n        \"output\": \" 6.9183097091893625e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H11Cl2NO2/c1-12-6-13(12,2)11(18)16(10(12)17)9-4-7(14)3-8(15)5-9/h3-5H,6H2,1-2H3\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][N][=C][Branch1][Ring1][C][#N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.862\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H13ClN2O/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\\n\",\n        \"output\": \" Diazepam\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H20NO5PS2/c1-5-14-10(13)11(4)9(12)8-19-17(18,15-6-2)16-7-3/h5-8H2,1-4H3\\n\",\n        \"output\": \" Mecarbam\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H10S2/c1-3-5-6-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" Diethyldisulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4BrCl/c7-5-1-3-6(8)4-2-5/h1-4H\\n\",\n        \"output\": \" 0.00023442288153199226 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Benzo(a)pyrene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H20Cl2O3/c1-21(2)17(12-18(22)23)19(21)20(24)25-13-14-7-6-10-16(11-14)26-15-8-4-3-5-9-15/h3-12,17,19H,13H2,1-2H3\\n\",\n        \"output\": \" Permethrin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H11NO2/c15-12-9-5-4-8-11(12)13(16)14-10-6-2-1-3-7-10/h1-9,15H,(H,14,16)\\n\",\n        \"output\": \" salicylanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2-Methyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H\\n\",\n        \"output\": \" Acenapthylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 2-Pentanol\\n\",\n        \"output\": \" -0.29\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Estragole\\n\",\n        \"output\": \" [C][Branch1][Ring1][O][C][=C][C][=C][Branch1][Ring2][C][C][=C][C][=C][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 4-Nitroacetanilide\\n\",\n        \"output\": \" -2.6919999999999997\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" 0.0005754399373371566 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Salicylamide\\n\",\n        \"output\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Aminophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Benfuracarb\\n\",\n        \"output\": \" -4.71\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Clc1cccc(Cl)c1\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cc2ccccc2cc1C\\n\",\n        \"output\": \" 2,3-Dimethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Ethanoyloxymethylphenytoin\\n\",\n        \"output\": \" InChI=1S/C18H16N2O4/c1-13(21)24-12-20-16(22)18(19-17(20)23,14-8-4-2-5-9-14)15-10-6-3-7-11-15/h2-11H,12H2,1H3,(H,19,23)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCC(=O)OC3(C(C)CC4C2CCC1=CC(=O)C=CC1(C)C2(F)C(O)CC34C)C(=O)CO\\n\",\n        \"output\": \" -4.71\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Methylphenol\\n\",\n        \"output\": \" Cc1cccc(O)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ccccc1N\\n\",\n        \"output\": \" o-Toluidine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C9H18O/c1-3-4-5-6-7-8-9(2)10/h3-8H2,1-2H3\\n\",\n        \"output\": \" -2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Hydrocortisone \\n\",\n        \"output\": \" InChI=1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Tetrahydrofurane \\n\",\n        \"output\": \" InChI=1S/C4H8O/c1-2-4-5-3-1/h1-4H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" C=Cc1ccccc1\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Benzo(e)pyrene\\n\",\n        \"output\": \" c1ccc2c(c1)c3cccc4ccc5cccc2c5c43\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Neburon\\n\",\n        \"output\": \" [C][C][C][C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C]\\n\",\n        \"output\": \" Propylene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-5(2)7(8)6(3)4/h5-8H,1-4H3\\n\",\n        \"output\": \" 2,4-Dimethyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Dienestrol\\n\",\n        \"output\": \" 1.122018454301963e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Hexylbenzene \\n\",\n        \"output\": \" 6.165950018614822e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C9H13ClN6/c1-4-12-7-13-6(10)14-8(15-7)16-9(2,3)5-11/h4H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" -3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H15O4P/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Niridazole\\n\",\n        \"output\": \" InChI=1S/C6H6N4O3S/c11-5-7-1-2-9(5)6-8-3-4(14-6)10(12)13/h3H,1-2H2,(H,7,11)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methyl benzoate \\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Brc1ccccc1\\n\",\n        \"output\": \" Bromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][Ring1][=N]\\n\",\n        \"output\": \" -5.64\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)c1ccc(C)cc1O\\n\",\n        \"output\": \" Thymol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][O][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C]\\n\",\n        \"output\": \" 0.0033265955329400436 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Hexanoyloxymethylphenyltoin\\n\",\n        \"output\": \" [O][=C][N][Branch1][N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][#C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" hydrobenzoin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccccc1N(=O)=O\\n\",\n        \"output\": \" -2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-2-10-7-8-11-5-3-4-6-12(11)9-10/h3-9H,2H2,1H3\\n\",\n        \"output\": \" 2-Ethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H24O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h3-11H2,1-2H3\\n\",\n        \"output\": \" Ethyl decanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Lactose\\n\",\n        \"output\": \" OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methylnapthalene\\n\",\n        \"output\": \" InChI=1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cyclooctyl-5-spirobarbituric acid\\n\",\n        \"output\": \" O=C2NC(=O)C1(CCCCCCC1)C(=O)N2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][S][C][C][C]\\n\",\n        \"output\": \" 0.0002951209226666387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Heptane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chlorbufam\\n\",\n        \"output\": \" InChI=1S/C11H10ClNO2/c1-3-8(2)15-11(14)13-10-6-4-5-9(12)7-10/h1,4-8H,2H3,(H,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Cl)(Cl)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" Hexachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][O][C][=Branch1][C][=O][NH1][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.001475706533275893 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Perylene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][C][=C][C][=C][C][=C][C][=C][C][Branch1][=N][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=Ring1][=N][=C][Ring1][=Branch2][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" -4.63\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Formothion\\n\",\n        \"output\": \" -1.995\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methyl nonanoate\\n\",\n        \"output\": \" InChI=1S/C10H20O2/c1-3-4-5-6-7-8-9-10(11)12-2/h3-9H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Eugenol\\n\",\n        \"output\": \" InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3,5-7,11H,1,4H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3,5-Dimethylphenol\\n\",\n        \"output\": \" Cc1cc(C)cc(O)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C]\\n\",\n        \"output\": \" Heptane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Butylbenzene\\n\",\n        \"output\": \" InChI=1S/C10H14/c1-2-3-7-10-8-5-4-6-9-10/h4-6,8-9H,2-3,7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Diethyldisulfide\\n\",\n        \"output\": \" -2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-5(9)6(10)2-4(3)8/h1-2,10H\\n\",\n        \"output\": \" -2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CH3I/c1-2/h1H3\\n\",\n        \"output\": \" Iodomethane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H3N3O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H\\n\",\n        \"output\": \" -2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CC(C)C\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Pentachlorophenol\\n\",\n        \"output\": \" 5.248074602497723e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][=Branch2][C][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.2161860006463678e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C18H22O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,17-20H,3-4H2,1-2H3\\n\",\n        \"output\": \" Hexestrol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(11)5(9)6(10)4(2)8/h1,11H\\n\",\n        \"output\": \" -3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" O-Ethyl carbamate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)CCC\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClCCCl\\n\",\n        \"output\": \" 1,2-Dichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4Br2/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" 0.00031622776601683794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-2-5-8-6-3-4-7-8/h8H,2-7H2,1H3\\n\",\n        \"output\": \" 1.8197008586099827e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-2-3-4-5-6/h6H,2-5H2,1H3\\n\",\n        \"output\": \" 1-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Thiophenol \\n\",\n        \"output\": \" Sc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" DDT\\n\",\n        \"output\": \" Clc1ccc(cc1)C(c2ccc(Cl)cc2)C(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C20H30O4/c1-3-5-7-11-15-23-19(21)17-13-9-10-14-18(17)20(22)24-16-12-8-6-4-2/h9-10,13-14H,3-8,11-12,15-16H2,1-2H3\\n\",\n        \"output\": \" Dihexyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" Difenoxuron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Tetrachloroethylene\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Androsterone\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][C][O][C][C][Ring1][#Branch1][C][C][C][C][Ring1][O][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H12N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)\\n\",\n        \"output\": \" -3.15\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" gentisin\\n\",\n        \"output\": \" c1c(O)C2C(=O)C3cc(O)ccC3OC2cc1(OC)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,3-Butadiene\\n\",\n        \"output\": \" C=CC=C\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 0.5128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 7-methylpteridine\\n\",\n        \"output\": \" [C][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccc2c(c1)ccc3ccccc32\\n\",\n        \"output\": \" Phenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,2,4,5-Tetrabromobenzene\\n\",\n        \"output\": \" Brc1cc(Br)c(Br)cc1Br\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benzophenone\\n\",\n        \"output\": \" InChI=1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)CC(C)C\\n\",\n        \"output\": \" 2,4-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" NC(=O)c1ccccc1\\n\",\n        \"output\": \" Benzamide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccc(OP(=O)(Oc2cccc(C)c2)Oc3ccccc3C)cc1\\n\",\n        \"output\": \" Tricresyl phosphate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1c2ccccc2c(C)c3ccccc13\\n\",\n        \"output\": \" -6.57\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H8/c1-3-5-4-2/h3-4H,1-2,5H2\\n\",\n        \"output\": \" 1,4-Pentadiene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-5(2)3-4-6/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 0.30902954325135906 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H8Cl6/c13-8-9(14)11(16)7-5-2-1-4(3-5)6(7)10(8,15)12(11,17)18/h1-2,4-7H,3H2\\n\",\n        \"output\": \" Aldrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Quinoline\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)=CCCC(O)(C)C=C\\n\",\n        \"output\": \" linalool\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCC(CC)COC(=O)c1ccccc1C(=O)OCC(CC)CCCC\\n\",\n        \"output\": \" Di(2-ethylhexyl)-phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][NH1][C][=Ring1][Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" -1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Hexachloro-1,3-butadiene\\n\",\n        \"output\": \" ClC(=C(Cl)C(=C(Cl)Cl)Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Butoxyethanol\\n\",\n        \"output\": \" InChI=1S/C6H14O2/c1-2-3-5-8-6-4-7/h7H,2-6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Br)Br\\n\",\n        \"output\": \" Chlorodibromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Oxamyl\\n\",\n        \"output\": \" CNC(=O)ON=C(SC)C(=O)N(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2-Dibromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4Br2/c7-5-3-1-2-4-6(5)8/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 7,12-Dimethylbenz(a)anthracene\\n\",\n        \"output\": \" InChI=1S/C20H16/c1-13-16-8-5-6-9-17(16)14(2)20-18(13)12-11-15-7-3-4-10-19(15)20/h3-12H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Isoprocarb\\n\",\n        \"output\": \" 0.0013708817661648536 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Methyl hexanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(Cl)CCl\\n\",\n        \"output\": \" 1,2-Dichloropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" o-Aminophenol\\n\",\n        \"output\": \" Nc1ccccc1O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCC(O)CC\\n\",\n        \"output\": \" -1.47\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Decalin\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][S][C][C][C]\\n\",\n        \"output\": \" Pebulate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ametryn\\n\",\n        \"output\": \" InChI=1S/C9H17N5S/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][O][Ring1][Branch1]\\n\",\n        \"output\": \" 1.288249551693134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Terbufos\\n\",\n        \"output\": \" 1.757923613958693e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][O][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][C][Branch1][#Branch1][C][O][C][Ring1][Branch1][=O][C][Branch2][Ring1][#Branch1][O][C][O][C][C][O][C][Branch1][C][C][O][C][Ring1][#Branch1][C][Branch1][C][O][C][Ring1][N][O][C][=C][C][O][C][O][C][=Ring1][Branch1][C][=C][Ring2][Ring1][#C][Ring1][=Branch2]\\n\",\n        \"output\": \" -3.571\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Terbutryn\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12O6/c7-1-3-4(9)5(10)6(11,2-8)12-3/h3-5,7-11H,1-2H2\\n\",\n        \"output\": \" Fructose\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Hexanol\\n\",\n        \"output\": \" CCCCC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Di(2-ethylhexyl)-phthalate\\n\",\n        \"output\": \" -6.96\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H13NO4/c1-12-11(13)16-9-5-3-2-4-8(9)10-14-6-7-15-10/h2-5,10H,6-7H2,1H3,(H,12,13)\\n\",\n        \"output\": \" Dioxacarb\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethalfluralin\\n\",\n        \"output\": \" [C][C][N][Branch1][#Branch1][C][C][Branch1][C][C][=C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methylphenanthrene\\n\",\n        \"output\": \" -5.84\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ipazine\\n\",\n        \"output\": \" InChI=1S/C10H18ClN5/c1-5-16(6-2)10-14-8(11)13-9(15-10)12-7(3)4/h7H,5-6H2,1-4H3,(H,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methoprene\\n\",\n        \"output\": \" [C][O][C][Branch1][C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][Branch1][C][C][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" DDE\\n\",\n        \"output\": \" ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dimethoxymethane\\n\",\n        \"output\": \" COCOC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Ethyl-p-hydroxybenzoate \\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Salicin\\n\",\n        \"output\": \" InChI=1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H22ClF3N2O3/c1-16(2)24(32-22-12-11-18(14-21(22)27)26(28,29)30)25(33)35-23(15-31)17-7-6-10-20(13-17)34-19-8-4-3-5-9-19/h3-14,16,23-24,32H,1-2H3\\n\",\n        \"output\": \" Fluvalinate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Ethylnaphthalene\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][O]\\n\",\n        \"output\": \" 2-Ethyl-1-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC(=O)CC\\n\",\n        \"output\": \" Ethyl propionate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)\\n\",\n        \"output\": \" Chlorzoxazone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Sc1ccccc1\\n\",\n        \"output\": \" 0.007585775750291836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Hexachloro-1,3-butadiene\\n\",\n        \"output\": \" [Cl][C][=Branch1][=C][=C][Branch1][C][Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\\n\",\n        \"output\": \" Dieldrin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc2c(N)c(=O)n(c1ccccc1)n2C\\n\",\n        \"output\": \" ampyrone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccc(N)cc1\\n\",\n        \"output\": \" p-Methylaniline \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1c2ccccc2c(C)c3ccc4ccccc4c13\\n\",\n        \"output\": \" -7.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 0.00017378008287493763 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Napthacene\\n\",\n        \"output\": \" c1ccc2cc3cc4ccccc4cc3cc2c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" C1Cc2cccc3cccc1c23\\n\",\n        \"output\": \" -4.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=N][N][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" Triazolam\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Hydrocortisone 21-acetate\\n\",\n        \"output\": \" InChI=1S/C23H32O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h10,16-18,20,26,28H,4-9,11-12H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1cccc(C)c1NC(=O)c2cc(c(Cl)cc2O)S(N)(=O)=O\\n\",\n        \"output\": \" -3.79\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dioxacarb\\n\",\n        \"output\": \" CNC(=O)Oc1ccccc1C2OCCO2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCC(C)CC\\n\",\n        \"output\": \" 3-Methylheptane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Oxamyl\\n\",\n        \"output\": \" 0.106\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Parathion\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Anthracene\\n\",\n        \"output\": \" InChI=1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 2,3,4,5-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" benodanil\\n\",\n        \"output\": \" 6.165950018614822e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" Fluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-Chloronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" trans-1,4-Dimethylcyclohexane\\n\",\n        \"output\": \" C/C1CCC(\\\\C)CC1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC(C)CCCO\\n\",\n        \"output\": \" -1.14\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Fc1cccc(F)c1\\n\",\n        \"output\": \" 1,3-Difluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Formothion\\n\",\n        \"output\": \" COP(=S)(OC)SCC(=O)N(C)C=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3\\n\",\n        \"output\": \" 2-Nonanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2-Hydroxypyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" t-Pentylbenzene\\n\",\n        \"output\": \" CC(C)(C)Cc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H2Cl2/c1-2(3)4/h1H2\\n\",\n        \"output\": \" 1,1-Dichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" hematein\\n\",\n        \"output\": \" InChI=1S/C16H12O6/c17-10-2-1-8-13-9-4-12(19)11(18)3-7(9)5-16(13,21)6-22-15(8)14(10)20/h1-4,17,19-21H,5-6H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" chlordimeform\\n\",\n        \"output\": \" CN(C)C=Nc1ccc(Cl)cc1C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 2,6-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Hydrocortisone 21-acetate\\n\",\n        \"output\": \" CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3C(O)CC21C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-2-4-7(8)5-6/h2-5H,8H2,1H3\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benomyl\\n\",\n        \"output\": \" CCCCNC(=O)n1c(NC(=O)OC)nc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" m-Fluorobromobenzene\\n\",\n        \"output\": \" [F][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CN(C)c1ccccc1\\n\",\n        \"output\": \" 0.012022644346174132 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Methyl propionate\\n\",\n        \"output\": \" CCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC(=C)C\\n\",\n        \"output\": \" 2-Methyl-1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CSc1nc(NC(C)C)nc(NC(C)C)n1\\n\",\n        \"output\": \" -4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H3Cl3/c3-1-2(4)5/h2H,1H2\\n\",\n        \"output\": \" 1,1,2-Trichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" m-Methylaniline\\n\",\n        \"output\": \" Cc1cccc(N)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Antipyrene\\n\",\n        \"output\": \" Cc1cc(=O)n(c2ccccc2)n1C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC/C=C\\\\C\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\\n\",\n        \"output\": \" -3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Octanol\\n\",\n        \"output\": \" InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Methyl-2-pentanol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" ClCCBr\\n\",\n        \"output\": \" 0.047863009232263824 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Mebendazole\\n\",\n        \"output\": \" COC(=O)Nc2nc1ccc(cc1[nH]2)C(=O)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Nonanol\\n\",\n        \"output\": \" CCCCCCCC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,3,4-Trimethylpentane\\n\",\n        \"output\": \" CC(C)C(C)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCCC(=O)OC\\n\",\n        \"output\": \" -1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2\\n\",\n        \"output\": \" 6.456542290346549e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" m-Fluorobromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4BrF/c7-5-2-1-3-6(8)4-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C20H20N2O4/c1-2-9-17(23)26-14-22-18(24)20(21-19(22)25,15-10-5-3-6-11-15)16-12-7-4-8-13-16/h3-8,10-13H,2,9,14H2,1H3,(H,21,25)\\n\",\n        \"output\": \" 8.491804750363127e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1,4-Cyclohexadiene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H26O3/c1-3-19(22)10-8-16-15-5-4-13-12-14(21)6-11-20(13,23)17(15)7-9-18(16,19)2/h1,12,15-17,22-23H,4-11H2,2H3\\n\",\n        \"output\": \" Norethisterone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C22H14/c1-3-7-17-15(5-1)9-11-21-19(17)13-14-20-18-8-4-2-6-16(18)10-12-22(20)21/h1-14H\\n\",\n        \"output\": \" -7.87\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-Heptanol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][O][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" c1ccc2c(c1)c3cccc4cccc2c34\\n\",\n        \"output\": \" 1e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1cc(Cl)ccc1Oc2ccc(Cl)cc2Cl\\n\",\n        \"output\": \" Triclosan\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Octanone\\n\",\n        \"output\": \" InChI=1S/C8H16O/c1-3-4-5-6-7-8(2)9/h3-7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H15N5S/c1-12(2)6-9-7(13(3)4)11-8(10-6)14-5/h1-5H3\\n\",\n        \"output\": \" -2.676\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Di-n-propylsulfide\\n\",\n        \"output\": \" CCCSCCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" -7.32\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Benzene \\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1cc(Cl)cc(Cl)c1Cl\\n\",\n        \"output\": \" 2,3,5-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2,4-Dimethylpentane\\n\",\n        \"output\": \" 5.495408738576248e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1cccnc1C\\n\",\n        \"output\": \" 2,3-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ipazine\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,1,1-Trichloroethane\\n\",\n        \"output\": \" InChI=1S/C2H3Cl3/c1-2(3,4)5/h1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C][C][C]\\n\",\n        \"output\": \" 0.01778279410038923 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][Branch1][Ring2][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][O][=O]\\n\",\n        \"output\": \" 0.009638290236239706 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" 5-(3-Methyl-2-butenyl)-5-ethylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Xipamide\\n\",\n        \"output\": \" Cc1cccc(C)c1NC(=O)c2cc(c(Cl)cc2O)S(N)(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][=Branch2][C]\\n\",\n        \"output\": \" Pentamethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C23H32O2/c1-14-12-17-18(21(3)9-6-16(25)13-20(14)21)7-11-23(5)19(17)8-10-22(23,4)15(2)24/h12-13,17-19H,6-11H2,1-5H3\\n\",\n        \"output\": \" 5.370317963702533e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Hexanone\\n\",\n        \"output\": \" CCCCC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H12N2S/c1-3-6-5(8)7-4-2/h3-4H2,1-2H3,(H2,6,7,8)\\n\",\n        \"output\": \" 1,3-diethylthiourea\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" o-Xylene \\n\",\n        \"output\": \" InChI=1S/C8H10/c1-7-5-3-4-6-8(7)2/h3-6H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H15NO3/c1-8(2)14-9-6-4-5-7-10(9)15-11(13)12-3/h4-8H,1-3H3,(H,12,13)\\n\",\n        \"output\": \" Propoxur\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC1(C)C(C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2)C1(C)C\\n\",\n        \"output\": \" Fenpropathrin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" m-Chloroaniline\\n\",\n        \"output\": \" [N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" Risocaine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-4-5-6-7-8(2,3)9/h9H,4-7H2,1-3H3\\n\",\n        \"output\": \" 2-Methyl-2-heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Testosterone\\n\",\n        \"output\": \" -4.02\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Thiophenol \\n\",\n        \"output\": \" InChI=1S/C6H6S/c7-6-4-2-1-3-5-6/h1-5,7H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" Eicosane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Hexylbenzene \\n\",\n        \"output\": \" [C][C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCC(=O)C\\n\",\n        \"output\": \" 2-Heptanone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSP(=S)(OCC)OCC\\n\",\n        \"output\": \" Ethion\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][O][C][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Ring1][P]\\n\",\n        \"output\": \" Carbetamide\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Malathion\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Nonene \\n\",\n        \"output\": \" CCCCCCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" diisooctyl phthalate\\n\",\n        \"output\": \" [C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][=C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][=C][Ring2][Ring1][N]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 5-Ethyl-5-isopropylbarbituric acid\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 9-Methylanthracene\\n\",\n        \"output\": \" -5.89\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H10/c1-7-5-3-4-6-8(7)2/h3-6H,1-2H3\\n\",\n        \"output\": \" o-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" NS(=O)(=O)c1cc(ccc1Cl)C2(O)NC(=O)c3ccccc23\\n\",\n        \"output\": \" -3.451\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C22H18Cl2FNO3/c1-22(2)15(11-19(23)24)20(22)21(27)29-18(12-26)13-8-9-16(25)17(10-13)28-14-6-4-3-5-7-14/h3-11,15,18,20H,1-2H3\\n\",\n        \"output\": \" -7.337000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" c1c(NC(=O)OC(C)C(=O)NCC)cccc1\\n\",\n        \"output\": \" 0.014791083881682071 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C20H12/c1-5-13-6-2-11-17-18-12-4-8-14-7-3-10-16(20(14)18)15(9-1)19(13)17/h1-12H\\n\",\n        \"output\": \" 1.5703628043335515e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" 0.0018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Propanol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cycluron\\n\",\n        \"output\": \" CN(C)C(=O)NC1CCCCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(C(CC)c1ccc(O)cc1)c2ccc(O)cc2\\n\",\n        \"output\": \" Hexestrol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H20O6P2S3/c1-17-23(25,18-2)21-13-5-9-15(10-6-13)27-16-11-7-14(8-12-16)22-24(26,19-3)20-4/h5-12H,1-4H3\\n\",\n        \"output\": \" -6.237\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H13ClN2O/c1-4-9(2)15(3)12(16)14-11-7-5-10(13)6-8-11/h1,5-9H,2-3H3,(H,14,16)\\n\",\n        \"output\": \" Buturon\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Fenuron\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Fluorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Risocaine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" linalool\\n\",\n        \"output\": \" [C][C][Branch1][C][C][=C][C][C][C][Branch1][C][O][Branch1][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2-Propanol\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][S][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C]\\n\",\n        \"output\": \" 7.943282347242822e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" P,P'-DDE\\n\",\n        \"output\": \" ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 3,3-Dimethylpentane\\n\",\n        \"output\": \" 5.888436553555884e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Methaqualone\\n\",\n        \"output\": \" -2.925\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Lindane\\n\",\n        \"output\": \" -4.64\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4N4O/c11-6-9-3-4-5(10-6)8-2-1-7-4/h1-3H,(H,8,9,10,11)\\n\",\n        \"output\": \" 2-hydroxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Hydroxyprogesterone-17a\\n\",\n        \"output\": \" InChI=1S/C21H30O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h12,16-18,24H,4-11H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H6Cl8/c11-3-1-2-4(5(3)12)9(16)7(14)6(13)8(2,15)10(9,17)18/h2-5H,1H2\\n\",\n        \"output\": \" 1.380384264602884e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][=C][=C][C][Branch1][=Branch1][N][=Branch1][C][=O][=O][=C][Ring1][=Branch2][O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.03499451670283573 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C(C)C\\n\",\n        \"output\": \" 2,3-Dimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3\\n\",\n        \"output\": \" 1.4125375446227544 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,6-Dimethylpyridine\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cn1ccc(=O)[nH]c1=O\\n\",\n        \"output\": \" 1-methyluracil\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCNc1nc(NC(C)(C)C)nc(OC)n1\\n\",\n        \"output\": \" 0.0005767664633922509 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" Pyrene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCOC=O\\n\",\n        \"output\": \" Butyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H22O2/c1-3-4-5-6-7-8-9-10-11(12)13-2/h3-10H2,1-2H3\\n\",\n        \"output\": \" 2.0417379446695274e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Isopentyl acetate\\n\",\n        \"output\": \" 0.012022644346174132 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" isocarbamid\\n\",\n        \"output\": \" InChI=1S/C8H15N3O2/c1-6(2)5-10-8(13)11-4-3-9-7(11)12/h6H,3-5H2,1-2H3,(H,9,12)(H,10,13)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C21H21O4P/c1-16-11-13-19(14-12-16)23-26(22,24-20-9-6-7-17(2)15-20)25-21-10-5-4-8-18(21)3/h4-15H,1-3H3\\n\",\n        \"output\": \" 9.77237220955811e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H13ClN2/c1-8-6-9(11)4-5-10(8)12-7-13(2)3/h4-7H,1-3H3\\n\",\n        \"output\": \" -2.86\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3\\n\",\n        \"output\": \" -4.44\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,3,5-Tribromobenzene\\n\",\n        \"output\": \" Brc1cc(Br)cc(Br)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][Branch1][C][N][=O][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Dulcin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Chlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cyclohexane\\n\",\n        \"output\": \" [C][C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCC(=O)CC\\n\",\n        \"output\": \" 0.5248074602497725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Methylaniline \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H4Br2/c3-1-2-4/h1-2H2\\n\",\n        \"output\": \" 1,2-Dibromoethane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H15I/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\",\n        \"output\": \" 1-Iodoheptane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Acetamide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N]\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][=C][Branch1][S][C][=C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" 5.754399373371567e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][O][Ring1][Ring1]\\n\",\n        \"output\": \" 1,2-Propylene oxide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Trichlorfon\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][C][Branch1][C][O][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" FC(F)(Cl)C(F)(F)Cl\\n\",\n        \"output\": \" 1,2-Dichlorotetrafluoroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanone\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C9H10O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\",\n        \"output\": \" 0.004786300923226385 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Cyclooctanol\\n\",\n        \"output\": \" InChI=1S/C8H16O/c9-8-6-4-2-1-3-5-7-8/h8-9H,1-7H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2-Dichlorobenzene\\n\",\n        \"output\": \" Clc1ccccc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Ethylnaphthalene\\n\",\n        \"output\": \" InChI=1S/C12H12/c1-2-10-7-8-11-5-3-4-6-12(11)9-10/h3-9H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Cyclohexanone\\n\",\n        \"output\": \" O=C1CCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=O)c1ccccc1\\n\",\n        \"output\": \" Acetophenone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][P][Ring1][#Branch2]\\n\",\n        \"output\": \" Benzo(b)fluorene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCC(=O)OCC\\n\",\n        \"output\": \" Pentyl propanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Ethyl-3-pentanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][O][Branch1][Ring1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Fenarimol\\n\",\n        \"output\": \" OC(c1ccc(Cl)cc1)(c2cncnc2)c3ccccc3Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [O][=C][Branch1][=C][C][N][C][=C][N][=C][Ring1][Branch1][N][=Branch1][C][=O][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0015488166189124811 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Dulcin\\n\",\n        \"output\": \" -2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" hexacosane\\n\",\n        \"output\": \" InChI=1S/C26H54/c1-3-5-7-9-11-13-15-17-19-21-23-25-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-26H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C2H2/c1-2/h1-2H\\n\",\n        \"output\": \" 1.9498445997580451 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" m-Nitrotoluene\\n\",\n        \"output\": \" 0.003630780547701014 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCCCCC\\n\",\n        \"output\": \" 6.729766562843168e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pencycuron\\n\",\n        \"output\": \" InChI=1S/C19H21ClN2O/c20-16-12-10-15(11-13-16)14-22(18-8-4-5-9-18)19(23)21-17-6-2-1-3-7-17/h1-3,6-7,10-13,18H,4-5,8-9,14H2,(H,21,23)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Acetanilide\\n\",\n        \"output\": \" CC(=O)Nc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1CCCCCCC1\\n\",\n        \"output\": \" Cyclooctane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Butan-2-ol\\n\",\n        \"output\": \" CCC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC#C\\n\",\n        \"output\": \" 1-Pentyne\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Methylcyclopentane\\n\",\n        \"output\": \" 0.0005011872336272725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Iodopropane\\n\",\n        \"output\": \" InChI=1S/C3H7I/c1-3(2)4/h3H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,3-Dibromobenzene\\n\",\n        \"output\": \" Brc1cccc(Br)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Methyl butyrate\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Sparsomycin (3,8mg/ml)\\n\",\n        \"output\": \" [C][S][C][S][=Branch1][C][=O][C][C][Branch1][Ring1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][NH1][C][=Branch1][C][=O][NH1][C][Ring1][Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H\\n\",\n        \"output\": \" -1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1cc(Cl)cc(Cl)c1\\n\",\n        \"output\": \" 3,5-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C11H16N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h5H,4,6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" -2.253\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" OC4=C(C1CCC(CC1)c2ccc(Cl)cc2)C(=O)c3ccccc3C4=O\\n\",\n        \"output\": \" -5.931\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,2,4-tribromobenzene\\n\",\n        \"output\": \" [C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Branch1][C][Br][C][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][N][=C][NH1][N][=Ring1][Branch1]\\n\",\n        \"output\": \" Amitrole\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" 9.931160484209335e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H7Cl3O2/c13-7-1-3-11(9(15)5-7)17-12-4-2-8(14)6-10(12)16/h1-6,16H\\n\",\n        \"output\": \" 3.467368504525317e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Ethylene\\n\",\n        \"output\": \" 0.3981071705534972 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,1,2-Trichloroethane\\n\",\n        \"output\": \" ClCC(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Butylbenzene\\n\",\n        \"output\": \" [C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Buturon\\n\",\n        \"output\": \" InChI=1S/C12H13ClN2O/c1-4-9(2)15(3)12(16)14-11-7-5-10(13)6-8-11/h1,5-9H,2-3H3,(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)OC(C)C\\n\",\n        \"output\": \" Diisopropyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(C)(C)Cl\\n\",\n        \"output\": \" 2-Chloro-2-methylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1C(O)CCC2(C)CC3CCC4(C)C5(C)CC6OCC(C)CC6OC5CC4C3C=C21\\n\",\n        \"output\": \" Diosgenin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Acridine\\n\",\n        \"output\": \" c3ccc2nc1ccccc1cc2c3\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Flurochloridone\\n\",\n        \"output\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][Branch1][Ring1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Altretamine\\n\",\n        \"output\": \" -3.364\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 4-Chloroanisole\\n\",\n        \"output\": \" 0.0016595869074375613 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,2,3-Trimethylbutane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6H\\n\",\n        \"output\": \" 2.290867652767775e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.00017378008287493763 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,2,4-Trimethylpentane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccccc1\\n\",\n        \"output\": \" Toluene \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" d-Limonene\\n\",\n        \"output\": \" InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=Branch1][C][=S][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chlorazine\\n\",\n        \"output\": \" InChI=1S/C11H20ClN5/c1-5-16(6-2)10-13-9(12)14-11(15-10)17(7-3)8-4/h5-8H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H14N4OS/c1-8(2,3)5-6(13)12(9)7(14-4)11-10-5/h9H2,1-4H3\\n\",\n        \"output\": \" Metribuzin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pyrazinamide\\n\",\n        \"output\": \" [N][C][=Branch1][C][=O][C][=C][N][=C][C][=N][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3-Chloroanisole\\n\",\n        \"output\": \" InChI=1S/C7H7ClO/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Metribuzin\\n\",\n        \"output\": \" CSc1nnc(c(=O)n1N)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][Branch1][=C][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][Cl][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -6.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccccc1n3c(C)nc2ccccc2c3=O\\n\",\n        \"output\": \" Methaqualone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" p-Xylene \\n\",\n        \"output\": \" Cc1ccc(C)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O2/c1-4-7-6(3)8-5-2/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.37153522909717257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C][=C]\\n\",\n        \"output\": \" 2-Methyl-1,3-Butadiene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(=O)C\\n\",\n        \"output\": \" 2-Butanone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccc2c(c1)cc3ccc4cccc5ccc2c3c45\\n\",\n        \"output\": \" Benzo(a)pyrene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)c1nc(nc(n1)N(C)C)N(C)C\\n\",\n        \"output\": \" Altretamine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(=O)CC\\n\",\n        \"output\": \" 3-Pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2-Methyl-2-hexanol\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Flurochloridone\\n\",\n        \"output\": \" FC(F)(F)c1cccc(c1)N2CC(CCl)C(Cl)C2=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(C)(C)C\\n\",\n        \"output\": \" 2,2-Dimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOCC\\n\",\n        \"output\": \" Diethyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Hydroxypyridine\\n\",\n        \"output\": \" Oc1ccccn1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Perfluidone\\n\",\n        \"output\": \" Cc1cc(ccc1NS(=O)(=O)C(F)(F)F)S(=O)(=O)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2-Propylene oxide\\n\",\n        \"output\": \" InChI=1S/C3H6O/c1-3-2-4-3/h3H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,3-diethylthiourea\\n\",\n        \"output\": \" InChI=1S/C5H12N2S/c1-3-6-5(8)7-4-2/h3-4H2,1-2H3,(H2,6,7,8)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Methoxychlor\\n\",\n        \"output\": \" InChI=1S/C16H15Cl3O2/c1-20-13-7-3-11(4-8-13)15(16(17,18)19)12-5-9-14(21-2)10-6-12/h3-10,15H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" -0.18\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Testosterone\\n\",\n        \"output\": \" CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCc1c(C)nc(NCC)[nH]c1=O\\n\",\n        \"output\": \" Ethirimol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][Cl]\\n\",\n        \"output\": \" 0.003090295432513592 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\\n\",\n        \"output\": \" 0.00038018939632056124 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H7Cl/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\\n\",\n        \"output\": \" 2-Chlorotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Ethane\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Triamterene\\n\",\n        \"output\": \" Nc3nc(N)c2nc(c1ccccc1)c(N)nc2n3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1NC(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" Phenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Terbutryn\\n\",\n        \"output\": \" CCNc1nc(NC(C)(C)C)nc(SC)n1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OC(Cn1cncn1)(c2ccc(F)cc2)c3ccccc3F\\n\",\n        \"output\": \" Flutriafol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H6N4/c1-5-2-9-6-3-8-4-10-7(6)11-5/h2-4H,1H3\\n\",\n        \"output\": \" 0.13995873225726177 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H15N3O2/c1-10-9-12(18-13(17)15(2)3)16(14-10)11-7-5-4-6-8-11/h4-9H,1-3H3\\n\",\n        \"output\": \" Pyrolan\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Equilin\\n\",\n        \"output\": \" InChI=1S/C18H20O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3-5,10,14,16,19H,2,6-9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -6.02\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][#N]\\n\",\n        \"output\": \" -2.168\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H18/c1-6(2)8(5)7(3)4/h6-8H,1-5H3\\n\",\n        \"output\": \" 1.584893192461114e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 3,4-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Sulfallate\\n\",\n        \"output\": \" InChI=1S/C8H14ClNS2/c1-4-10(5-2)8(11)12-6-7(3)9/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 3-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.0002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 5-Allyl-5-isopropylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(C(C)C)CC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O\\n\",\n        \"output\": \" Maltose\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 1,1,2-Trichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][=N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" 1.445439770745928e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" p-Cresol\\n\",\n        \"output\": \" -0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][C][=C][C][=C][O][Ring1][Branch1]\\n\",\n        \"output\": \" 0.7943282347242815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,3-Butadiene\\n\",\n        \"output\": \" InChI=1S/C4H6/c1-3-4-2/h3-4H,1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,1-Diethoxyethane \\n\",\n        \"output\": \" [C][C][O][C][Branch1][C][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" Parathion\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 1,2-Diethylbenzene\\n\",\n        \"output\": \" 0.0005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H2Cl4/c7-3-1-2-4(8)6(10)5(3)9/h1-2H\\n\",\n        \"output\": \" -4.57\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][/C][=C][/C]\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-4-5-6-7-8(2,3)9/h9H,4-7H2,1-3H3\\n\",\n        \"output\": \" 0.019054607179632473 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Vinclozolin\\n\",\n        \"output\": \" InChI=1S/C12H9Cl2NO3/c1-3-12(2)10(16)15(11(17)18-12)9-5-7(13)4-8(14)6-9/h3-6H,1H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][=O]\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1]\\n\",\n        \"output\": \" -7.01\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Phenoxyethanol\\n\",\n        \"output\": \" InChI=1S/C8H10O2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Formetanate\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][Branch1][Branch2][N][=C][N][Branch1][C][C][C][=C][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CN(C)C(=O)NC1CC2CC1C3CCCC23\\n\",\n        \"output\": \" 0.0006745280276979215 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H6N4/c1-5-10-4-6-7(11-5)9-3-2-8-6/h2-4H,1H3\\n\",\n        \"output\": \" 0.7585775750291838 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.00021877616239495518 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=C)C(=C)C\\n\",\n        \"output\": \" 2,3-Dimethyl-1,3-Butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2-Dichloroethane\\n\",\n        \"output\": \" InChI=1S/C2H4Cl2/c3-1-2-4/h1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Anthraquinone\\n\",\n        \"output\": \" O=C1c2ccccc2C(=O)c3ccccc13\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Diethyl phthalate \\n\",\n        \"output\": \" CCOC(=O)c1ccccc1C(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][C][C][C][=Branch1][C][=O][N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9952623149688795 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc3nnc4CN=C(c1ccccc1Cl)c2cc(Cl)ccc2n34\\n\",\n        \"output\": \" Triazolam\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" P,P'-DDE\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCc1ccccc1\\n\",\n        \"output\": \" Butylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cn1cnc2n(C)c(=O)n(C)c(=O)c12\\n\",\n        \"output\": \" Caffeine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H14ClNO2/c1-12(2)8-16-14(11(12)15)7-9-5-3-4-6-10(9)13/h3-6H,7-8H2,1-2H3\\n\",\n        \"output\": \" Clomazone\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methylpropene\\n\",\n        \"output\": \" InChI=1S/C4H8/c1-4(2)3/h1H2,2-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" 2.0417379446695274e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cc(Cl)c(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" Pentachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Chlorobiphenyl\\n\",\n        \"output\": \" [C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CNc2cnn(c1cccc(c1)C(F)(F)F)c(=O)c2Cl\\n\",\n        \"output\": \" 8.994975815300346e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" p-Hydroxyacetanilide\\n\",\n        \"output\": \" 0.0933254300796991 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" Ethyl propionate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2,6-Dimethylphenol\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H6Cl4/c13-8-2-4-10(14)9(6-8)7-1-3-11(15)12(16)5-7/h1-6H\\n\",\n        \"output\": \" 5.6234132519034905e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H10/c1-5(2)6(3)4/h1,3H2,2,4H3\\n\",\n        \"output\": \" 2,3-Dimethyl-1,3-Butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H16N2O4/c1-11-5-3-6-12(9-11)18-16(20)22-14-8-4-7-13(10-14)17-15(19)21-2/h3-10H,1-2H3,(H,17,19)(H,18,20)\\n\",\n        \"output\": \" Phenmedipham\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" -0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H12/c1-2-4-6-7-5-3-1/h1-2H,3-7H2\\n\",\n        \"output\": \" -3.18\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Dibenzothiophene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Iodobutane\\n\",\n        \"output\": \" CCCCI\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Propetamphos\\n\",\n        \"output\": \" InChI=1S/C10H20NO4PS/c1-6-11-16(17,13-5)15-9(4)7-10(12)14-8(2)3/h7-8H,6H2,1-5H3,(H,11,17)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" d-inositol\\n\",\n        \"output\": \" OC1C(O)C(O)C(O)C(O)C1O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -6.0\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Heptane\\n\",\n        \"output\": \" -4.53\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H7ClO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3\\n\",\n        \"output\": \" 4-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C22H19ClO3/c23-16-11-9-14(10-12-16)13-5-7-15(8-6-13)19-20(24)17-3-1-2-4-18(17)21(25)22(19)26/h1-4,9-13,15,26H,5-8H2\\n\",\n        \"output\": \" -5.931\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1cc(C)c2ccccc2c1\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCC\\n\",\n        \"output\": \" -2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlorazine\\n\",\n        \"output\": \" CCN(CC)c1nc(Cl)nc(n1)N(CC)CC\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H4BrCl/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" o-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Hexene-3-ol\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-3-5-6(7)4-2/h4,6-7H,2-3,5H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2,3,5-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Napthalene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][=O]\\n\",\n        \"output\": \" Valeraldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Pentadecanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H3\\n\",\n        \"output\": \" 4-Isopropyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.0009120108393559096 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][O]\\n\",\n        \"output\": \" -5.03\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" m-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H10ClN3O3/c16-12-4-2-1-3-10(12)15-11-7-9(19(21)22)5-6-13(11)18-14(20)8-17-15/h1-7H,8H2,(H,18,20)\\n\",\n        \"output\": \" Clonazepam\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Simetryn\\n\",\n        \"output\": \" InChI=1S/C8H15N5S/c1-12(2)6-9-7(13(3)4)11-8(10-6)14-5/h1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Ethanethiol\\n\",\n        \"output\": \" 0.251188643150958 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dinitramine\\n\",\n        \"output\": \" CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][C][=C][C][C][Ring1][Branch1][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl]\\n\",\n        \"output\": \" Heptachlor\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Carbophenthion\\n\",\n        \"output\": \" 1.8365383433483438e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethofumesate\\n\",\n        \"output\": \" InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Branch1][C][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.00044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC1CCCC1\\n\",\n        \"output\": \" -3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Bensulide\\n\",\n        \"output\": \" InChI=1S/C14H24NO4PS3/c1-12(2)18-20(21,19-13(3)4)22-11-10-15-23(16,17)14-8-6-5-7-9-14/h5-9,12-13,15H,10-11H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(C)Nc1nc(Cl)nc(NC(C)C)n1\\n\",\n        \"output\": \" 3.715352290971728e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2.9512092266663856 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H8Cl3O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\\n\",\n        \"output\": \" Ronnel\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3\\n\",\n        \"output\": \" Carvacrol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl hexanoate\\n\",\n        \"output\": \" InChI=1S/C8H16O2/c1-3-5-6-7-8(9)10-4-2/h3-7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Butyraldehyde\\n\",\n        \"output\": \" CCCC=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" Octane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Diisopropyl ether \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" hydrobenzoin\\n\",\n        \"output\": \" 0.011748975549395297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1cccc2c1ccc3ccccc32\\n\",\n        \"output\": \" 1.4125375446227554e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" 0.013489628825916533 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 6-Methylchrysene\\n\",\n        \"output\": \" -6.57\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" iran\\n\",\n        \"output\": \" iran does not have InChI\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Cc1cc(C)c(C)cc1C\\n\",\n        \"output\": \" 2.5703957827688645e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(OC(=O)Nc1cccc(Cl)c1)C#C\\n\",\n        \"output\": \" Chlorbufam\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCI\\n\",\n        \"output\": \" 0.0010964781961431851 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Benfluralin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO\\n\",\n        \"output\": \" 0.0008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c2ccc1[nH]nnc1c2\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.9810717055349695e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Methyl-3-hexanol\\n\",\n        \"output\": \" CCCC(C)(O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.06025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-7-5-4-6-8(2)9(7)3/h4-6H,1-3H3\\n\",\n        \"output\": \" 1,2,3-Trimethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Abate\\n\",\n        \"output\": \" InChI=1S/C16H20O6P2S3/c1-17-23(25,18-2)21-13-5-9-15(10-6-13)27-16-11-7-14(8-12-16)22-24(26,19-3)20-4/h5-12H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" -6.291\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Triclosan\\n\",\n        \"output\": \" InChI=1S/C12H7Cl3O2/c13-7-1-3-11(9(15)5-7)17-12-4-2-8(14)6-10(12)16/h1-6,16H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCCCCCCCCCCC\\n\",\n        \"output\": \" hexacosane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Acetophenone\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Bendroflumethiazide\\n\",\n        \"output\": \" InChI=1S/C15H14F3N3O4S2/c16-15(17,18)10-7-11-13(8-12(10)26(19,22)23)27(24,25)21-14(20-11)6-9-4-2-1-3-5-9/h1-5,7-8,14,20-21H,6H2,(H2,19,22,23)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch1][C][=C][Ring1][Branch1][C][Ring1][#Branch1][C][Ring1][=N][Branch1][C][Cl][C][Ring1][N][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Aldrin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3,4-Dimethylpyridine\\n\",\n        \"output\": \" [C][C][=C][C][=N][C][=C][Ring1][=Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,4-Dinitrotoluene\\n\",\n        \"output\": \" Cc1ccc(cc1N(=O)=O)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methyl-2-heptanol\\n\",\n        \"output\": \" InChI=1S/C8H18O/c1-4-5-6-7-8(2,3)9/h9H,4-7H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][Cl]\\n\",\n        \"output\": \" 1-Chlorobutane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc1cc(C)nc(n1)C(C)C\\n\",\n        \"output\": \" 0.00022908676527677723 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 4-hydroxypyridine\\n\",\n        \"output\": \" InChI=1S/C5H5NO/c7-5-1-3-6-4-2-5/h1-4H,(H,6,7)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,3-Dichloronitrobenzene\\n\",\n        \"output\": \" O=N(=O)c1c(Cl)c(Cl)ccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" ClC1(C(=O)C2(Cl)C3(Cl)C14Cl)C5(Cl)C2(Cl)C3(Cl)C(Cl)(Cl)C45Cl\\n\",\n        \"output\": \" 5.508076964054041e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methylpropane\\n\",\n        \"output\": \" InChI=1S/C4H10/c1-4(2)3/h4H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-4-5-6(2)7/h3-5H2,1-2H3\\n\",\n        \"output\": \" 2-Hexanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Carbofuran\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][Ring1][O][=Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H12O4/c1-12-7-4-3-6-5-14-10(11)8(6)9(7)13-2/h3-4,6,8H,5H2,1-2H3\\n\",\n        \"output\": \" 0.012618275345906706 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H18N2O3/c1-4-6-8(3)12(7-5-2)9(15)13-11(17)14-10(12)16/h5,8H,2,4,6-7H2,1,3H3,(H2,13,14,15,16,17)\\n\",\n        \"output\": \" 0.0044055486350655345 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CSSC\\n\",\n        \"output\": \" 0.03630780547701014 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][S][C]\\n\",\n        \"output\": \" Dimethyl sulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Bromobutane\\n\",\n        \"output\": \" CCCCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" p-Hydroxybenzaldehyde \\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Benzonitrile\\n\",\n        \"output\": \" InChI=1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" p-Chloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Bromonapthalene\\n\",\n        \"output\": \" InChI=1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benzaldehyde\\n\",\n        \"output\": \" O=Cc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 5-Allyl-5-methylbarbital\\n\",\n        \"output\": \" -1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Progesterone\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring2][Ring1][Ring1][Ring1][S][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,3,6-Trichlorophenol\\n\",\n        \"output\": \" [O][C][=C][Branch1][C][Cl][C][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H16/c1-5-6-7(2,3)4/h5-6H2,1-4H3\\n\",\n        \"output\": \" -4.36\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2,3,5-Tetrachlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H6S/c1-3-2/h1-2H3\\n\",\n        \"output\": \" Dimethyl sulfide\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Amitrole\\n\",\n        \"output\": \" InChI=1S/C2H4N4/c3-2-4-1-5-6-2/h1H,(H3,3,4,5,6)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2,3-Trimethylbutane\\n\",\n        \"output\": \" CC(C)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" m-Nitrophenol\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-5-2-1-4(9)3-6(5)8/h1-3,9H\\n\",\n        \"output\": \" 3,4-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Nitrapyrin\\n\",\n        \"output\": \" Clc1cccc(n1)C(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(O)(CC)CC\\n\",\n        \"output\": \" 3-Ethyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Isopentyl formate\\n\",\n        \"output\": \" CC(C)CCOC=O\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methyl hexanoate\\n\",\n        \"output\": \" InChI=1S/C7H14O2/c1-3-4-5-6-7(8)9-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dienochlor\\n\",\n        \"output\": \" InChI=1S/C10Cl10/c11-1-2(12)6(16)9(19,5(1)15)10(20)7(17)3(13)4(14)8(10)18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1cccc(Cl)c1\\n\",\n        \"output\": \" 3-Chlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Risocaine\\n\",\n        \"output\": \" 0.00353183169791957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Metoxuron\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" COC(=O)C=C\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" 0.006165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Chlortoluron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1ccc(C)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Napthacene\\n\",\n        \"output\": \" 2.511886431509582e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" o-Chlorobromobenzene\\n\",\n        \"output\": \" -3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,2,4,6,6'-PCB\\n\",\n        \"output\": \" Clc1cc(Cl)c(c(Cl)c1)c2c(Cl)cccc2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2,3,4,5-Tetrachlorophenol\\n\",\n        \"output\": \" 0.000707945784384138 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Flumethasone\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][Branch1][C][F][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][Ring1][Branch1][C][C][C][Ring2][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H20ClN5/c1-5-16(6-2)10-13-9(12)14-11(15-10)17(7-3)8-4/h5-8H2,1-4H3\\n\",\n        \"output\": \" Chlorazine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][C]\\n\",\n        \"output\": \" Chloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1c(Cl)ccc(Cl)c1Cl\\n\",\n        \"output\": \" 2,3,6-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Bromochloromethane\\n\",\n        \"output\": \" ClCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H9ClNO5PS/c1-13-16(17,14-2)15-8-4-3-6(10(11)12)5-7(8)9/h3-5H,1-2H3\\n\",\n        \"output\": \" 4.897788193684466e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][=Branch2]\\n\",\n        \"output\": \" 1-Methylfluorene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3/c7-4-1-2-5(8)6(9)3-4/h1-3H\\n\",\n        \"output\": \" 1,2,4-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-Methyl-2-pentanone\\n\",\n        \"output\": \" CC(C)CC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H13BrN2O2/c1-3-7(8,4-2)5(11)10-6(9)12/h3-4H2,1-2H3,(H3,9,10,11,12)\\n\",\n        \"output\": \" Carbromal\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/CHBrCl2/c2-1(3)4/h1H\\n\",\n        \"output\": \" 0.028840315031266057 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3,5-Dimethylpyridine\\n\",\n        \"output\": \" Cc1cncc(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" -2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" XMC\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Methyl acrylate\\n\",\n        \"output\": \" InChI=1S/C4H6O2/c1-3-4(5)6-2/h3H,1H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Butane\\n\",\n        \"output\": \" InChI=1S/C4H10/c1-3-4-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CON(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" Linuron\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H7Cl2NO3/c13-8-1-6-12(11(14)7-8)18-10-4-2-9(3-5-10)15(16)17/h1-7H\\n\",\n        \"output\": \" -5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 5-Ethyl-5-(3-methylbutyl)barbital\\n\",\n        \"output\": \" 0.0021978598727848252 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H17ClN3O3PS/c1-5-14-17(18,15-6-2)16-9-11-8(10)13(12-9)7(3)4/h7H,5-6H2,1-4H3\\n\",\n        \"output\": \" Isazofos\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,6-Dimethylpyridine\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][C][C][=N][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C)CC\\n\",\n        \"output\": \" 5-Methyl-5-ethylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" NC(=O)c1cnccn1\\n\",\n        \"output\": \" Pyrazinamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [Br][C][C][Br]\\n\",\n        \"output\": \" 0.020892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methocarbamol\\n\",\n        \"output\": \" COc1ccccc1OCC(O)COC(N)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" ClCC(Cl)(Cl)Cl\\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" -8.017000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Oxamyl\\n\",\n        \"output\": \" InChI=1S/C7H13N3O3S/c1-8-7(12)13-9-5(14-4)6(11)10(2)3/h1-4H3,(H,8,12)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H7NO/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methyl butyrate\\n\",\n        \"output\": \" CCCOC(=O)CC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H20O2/c1-3-5-6-7-8-9-10(11)12-4-2/h3-9H2,1-2H3\\n\",\n        \"output\": \" 0.0004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)(C)CO\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCCCCCO\\n\",\n        \"output\": \" -3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][C][C][=C]\\n\",\n        \"output\": \" 0.7079457843841379 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Diphenylmethane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Benomyl\\n\",\n        \"output\": \" -4.883\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Hexyne \\n\",\n        \"output\": \" CCCCC#C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1c(cc(cc1N(=O)=O)N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" 2,4,6-Trinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Methylheptane\\n\",\n        \"output\": \" CCCCC(C)CC\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.6853444456585036e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,3,6-Trichlorophenol\\n\",\n        \"output\": \" Oc1c(Cl)ccc(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Phenetole\\n\",\n        \"output\": \" CCOc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2-Ethyl pyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Chlorodibromethane\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Br][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H7Br/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\\n\",\n        \"output\": \" 3.9810717055349695e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" 0.0001445439770745928 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3\\n\",\n        \"output\": \" Nonane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Methyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Furfural\\n\",\n        \"output\": \" [O][=C][C][=C][C][=C][O][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1cccnc1C\\n\",\n        \"output\": \" 2.3988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given SMILES? ->\",\n        \"input\": \" OC(C(=O)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Triamterene\\n\",\n        \"output\": \" [N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][N][=N][C][Ring1][=N][=N][Ring2][Ring1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h3-8H,1-2H3\\n\",\n        \"output\": \" 1.2882495516931348e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H16Cl2N2O/c1-3-4-7-16(2)12(17)15-9-5-6-10(13)11(14)8-9/h5-6,8H,3-4,7H2,1-2H3,(H,15,17)\\n\",\n        \"output\": \" Neburon\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCI\\n\",\n        \"output\": \" 1-Iodobutane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" o-Toluidine\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-4-2-3-5-7(6)8/h2-5H,8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" t-Pentylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" o-Nitroanisole\\n\",\n        \"output\": \" COc1ccccc1N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)CC(C)(C)C\\n\",\n        \"output\": \" -4.74\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Chlorotoluene\\n\",\n        \"output\": \" -3.52\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 4-Isopropyltoluene\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClCc1ccccc1\\n\",\n        \"output\": \" Benzylchloride\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,2,4-Trimethylpentane\\n\",\n        \"output\": \" -4.74\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2,3-Trichlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3Cl3/c7-4-2-1-3-5(8)6(4)9/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethane\\n\",\n        \"output\": \" [C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(O)C(C)C\\n\",\n        \"output\": \" 2-Methyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,2,4-tribromobenzene\\n\",\n        \"output\": \" 3.1622776601683795e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H16N2O3/c1-3-13-11(15)9(2)17-12(16)14-10-7-5-4-6-8-10/h4-9H,3H2,1-2H3,(H,13,15)(H,14,16)\\n\",\n        \"output\": \" -1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" p-Bromoiodobenzene\\n\",\n        \"output\": \" [Br][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Endrin\\n\",\n        \"output\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H20/c1-2-3-4-7-10-8-5-6-9-10/h10H,2-9H2,1H3\\n\",\n        \"output\": \" Pentylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Heptanol\\n\",\n        \"output\": \" CCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" Lindane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Cyclopentyl-5-spirobarbituric acid\\n\",\n        \"output\": \" -2.349\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Nonene \\n\",\n        \"output\": \" -5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 1.9054607179632483e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methyl-1-Butene\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 3-Hexanol\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-Hydroxyacetanilide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cccc2c1Cc3ccccc32\\n\",\n        \"output\": \" 1-Methylfluorene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.000239883291901949 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1(C#N)c(Cl)c(C#N)c(Cl)c(Cl)c(Cl)1\\n\",\n        \"output\": \" Chlorothalonil\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Terbufos\\n\",\n        \"output\": \" CCOP(=S)(OCC)SCSC(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" methyl laurate\\n\",\n        \"output\": \" 2.0417379446695274e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benfuracarb\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][C][N][Branch2][Ring1][=C][S][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][=Ring1][#Branch1][Ring1][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Dimefuron\\n\",\n        \"output\": \" -4.328\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Propoxur\\n\",\n        \"output\": \" -2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Endrin\\n\",\n        \"output\": \" ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6HCl5/c7-2-1-3(8)5(10)6(11)4(2)9/h1H\\n\",\n        \"output\": \" 2.2387211385683376e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methylcyclopentane\\n\",\n        \"output\": \" [C][C][C][C][C][C][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2,3,4-Tetrahydronapthalene\\n\",\n        \"output\": \" InChI=1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Cyclohexyl-5-spirobarbituric acid\\n\",\n        \"output\": \" -3.06\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Butamben\\n\",\n        \"output\": \" 0.0008279421637123345 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Carvacrol\\n\",\n        \"output\": \" 0.008317637711026709 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1,2,4-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" ClC(Cl)(Cl)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" 0.00021379620895022324 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" joseph\\n\",\n        \"output\": \" joseph does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 1,1-Dichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][O]\\n\",\n        \"output\": \" 1.0 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 2-Chlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" C#C\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Propazine\\n\",\n        \"output\": \" InChI=1S/C9H16ClN5/c1-5(2)11-8-13-7(10)14-9(15-8)12-6(3)4/h5-6H,1-4H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C2NC(=O)C1(CCCC1)C(=O)N2\\n\",\n        \"output\": \" Cyclopentyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" meconin\\n\",\n        \"output\": \" InChI=1S/C10H12O4/c1-12-7-4-3-6-5-14-10(11)8(6)9(7)13-2/h3-4,6,8H,5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Hexanol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Menthone\\n\",\n        \"output\": \" 0.0044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" COc1ccccc1Cl\\n\",\n        \"output\": \" 0.0034673685045253167 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Butanoyloxymethylphenytoin\\n\",\n        \"output\": \" O=C1N(COC(=O)CCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCCCl\\n\",\n        \"output\": \" 0.0007585775750291836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC(=O)c1ccccc1S(=O)(=O)NN(C=O)c2nc(Cl)cc(OC)n2\\n\",\n        \"output\": \" Chlorimuron-ethyl (ph 7)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethyl formate\\n\",\n        \"output\": \" CCOC=O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Clc1ccc(CN(C2CCCC2)C(=O)Nc3ccccc3)cc1\\n\",\n        \"output\": \" 1.2161860006463678e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3\\n\",\n        \"output\": \" Prasterone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H3Cl4N/c7-5-3-1-2-4(11-5)6(8,9)10/h1-3H\\n\",\n        \"output\": \" Nitrapyrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1c(Cl)cc(Cl)cc1Cl\\n\",\n        \"output\": \" 2,4,6-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Toluene \\n\",\n        \"output\": \" 0.006165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" Anthracene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3\\n\",\n        \"output\": \" Carvone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3\\n\",\n        \"output\": \" 1-Bromobutane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H18/c1-7(2)6-8(3,4)5/h7H,6H2,1-5H3\\n\",\n        \"output\": \" -4.74\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Nonyne \\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H7Cl/c1-2-3-4/h2-3H2,1H3\\n\",\n        \"output\": \" 1-Chloropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2-Dichloropropane\\n\",\n        \"output\": \" CC(Cl)CCl\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.518559443749226e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Ethyl benzoate \\n\",\n        \"output\": \" CCOC(=O)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" OCC(O)C(O)CO\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3,4-Dimethylphenol\\n\",\n        \"output\": \" InChI=1S/C8H10O/c1-6-3-4-8(9)5-7(6)2/h3-5,9H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Raffinose\\n\",\n        \"output\": \" 0.3890451449942806 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H11ClN2O4S/c15-11-6-5-8(7-12(11)22(16,20)21)14(19)10-4-2-1-3-9(10)13(18)17-14/h1-7,19H,(H,17,18)(H2,16,20,21)\\n\",\n        \"output\": \" Chlorthalidone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][C][C][C][Branch1][=Branch1][C][Ring1][=Branch2][=Ring1][Branch1][=C][Ring1][N][C][=C][Ring1][S]\\n\",\n        \"output\": \" 3-Methylcholanthrene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h19H,2-18H2,1H3\\n\",\n        \"output\": \" 1-Octadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Clc1cc(Cl)c(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" 2.2387211385683376e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Iodobenzene\\n\",\n        \"output\": \" Ic1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methylbutane\\n\",\n        \"output\": \" InChI=1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCCCCCCCCCC\\n\",\n        \"output\": \" Hexadecane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSP(=S)(OCC)OCC\\n\",\n        \"output\": \" -5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][N][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=O][N][=C][Ring1][Branch2][N][Branch1][S][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O][C][=Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][=Branch2][C]\\n\",\n        \"output\": \" 0.00020653801558105292 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H9Cl/c1-4(2)3-5/h4H,3H2,1-2H3\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" -1.11\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Chloro-2-bromoethane\\n\",\n        \"output\": \" -1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Pentanone\\n\",\n        \"output\": \" InChI=1S/C5H10O/c1-3-4-5(2)6/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H10/c1-5(2)6(3)4/h1,3H2,2,4H3\\n\",\n        \"output\": \" 0.003981071705534973 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl\\n\",\n        \"output\": \" -6.18\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Branch1][C][Br][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 1,2,4-tribromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 4-Nitroacetanilide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)\\n\",\n        \"output\": \" -1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][Branch1][C][O][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Chlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" o-Chloroaniline\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methyl-1,3-Butadiene \\n\",\n        \"output\": \" [C][C][=Branch1][C][=C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Decalin\\n\",\n        \"output\": \" InChI=1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" Butan-2-ol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(=O)OCC\\n\",\n        \"output\": \" Methyl pentanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H18/c1-7-8(2)10(4)12(6)11(5)9(7)3/h1-6H3\\n\",\n        \"output\": \" Hexamethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CNc1ccccc1\\n\",\n        \"output\": \" -1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" BrC(Br)(Br)Br\\n\",\n        \"output\": \" 0.0007244359600749898 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][Branch1][Branch2][N][=C][N][Branch1][C][C][C][=C][Ring1][O]\\n\",\n        \"output\": \" 0.004570881896148752 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" Nitramine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 5,5-Diisopropylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(C(C)C)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Kepone\\n\",\n        \"output\": \" ClC1(C(=O)C2(Cl)C3(Cl)C14Cl)C5(Cl)C2(Cl)C3(Cl)C(Cl)(Cl)C45Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dimecron\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cn2cc(c1ccccc1)c(=O)c(c2)c3cccc(c3)C(F)(F)F\\n\",\n        \"output\": \" Fluridone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Acenapthylene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1cc(C)cc2c1c3cc4cccc5CCc(c45)c3cc2\\n\",\n        \"output\": \" 1.202264434617413e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Butane\\n\",\n        \"output\": \" CCCC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 1,2,3,4-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H10O2/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O]\\n\",\n        \"output\": \" Dichlorophen\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0007762471166286919 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Hexyne \\n\",\n        \"output\": \" 0.004365158322401661 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC(C)=CCCC(C)=CC(=O)\\n\",\n        \"output\": \" -2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" Benzophenone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1,1,2-Trichlorotrifluoroethane\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H8/c1-2-4-5-3-1/h1-2H,3-5H2\\n\",\n        \"output\": \" -2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CSSC\\n\",\n        \"output\": \" Dimethyldisulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dichloromethane\\n\",\n        \"output\": \" ClCCl\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.018197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benzo(a)fluorene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][P][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Nitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][N][=C][NH1][N][=Ring1][Branch1]\\n\",\n        \"output\": \" 0.522\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][Cl]\\n\",\n        \"output\": \" 1,2-Dichlorotetrafluoroethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pentachloroethane\\n\",\n        \"output\": \" ClC(Cl)C(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCSCCC\\n\",\n        \"output\": \" Di-n-propylsulfide\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ioxynil\\n\",\n        \"output\": \" [O][C][=C][Branch1][C][I][C][=C][Branch1][Ring1][C][#N][C][=C][Ring1][=Branch2][I]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" O-Ethyl carbamate\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Heptane\\n\",\n        \"output\": \" CCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H15O3PS2/c1-8-7-9(5-6-10(8)16-4)13-14(15,11-2)12-3/h5-7H,1-4H3\\n\",\n        \"output\": \" 2.691534803926914e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" Dialifos\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Epitostanol\\n\",\n        \"output\": \" CC45CCC2C(CCC3CC1SC1CC23C)C4CCC5O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCBr\\n\",\n        \"output\": \" -3.08\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,8-Cineole\\n\",\n        \"output\": \" CC12CCC(CC1)C(C)(C)O2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,3,4,5-Tetrachlorophenol\\n\",\n        \"output\": \" Oc1cc(Cl)c(Cl)c(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" norethindrone acetate\\n\",\n        \"output\": \" CC(=O)OC3(CCC4C2CCC1=CC(=O)CCC1C2CCC34C)C#C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][N][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=N][C]\\n\",\n        \"output\": \" ampyrone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-2-3-4-5-6/h5H,2-4H2,1H3\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Propyne\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Butanol\\n\",\n        \"output\": \" InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3,5-7,11H,1,4H2,2H3\\n\",\n        \"output\": \" Eugenol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3\\n\",\n        \"output\": \" 1-Tetradecanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Flumetralin\\n\",\n        \"output\": \" -6.78\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CNC(=O)Oc1cc(C)cc(C)c1\\n\",\n        \"output\": \" 0.0026242185433844392 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H10Cl2F3NO/c13-5-7-6-18(11(19)10(7)14)9-3-1-2-8(4-9)12(15,16)17/h1-4,7,10H,5-6H2\\n\",\n        \"output\": \" -4.047\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H6N4O3S/c11-5-7-1-2-9(5)6-8-3-4(14-6)10(12)13/h3H,1-2H2,(H,7,11)\\n\",\n        \"output\": \" Niridazole\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)COC=O\\n\",\n        \"output\": \" Isobutyl formate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1,2-Dichlorobenzene\\n\",\n        \"output\": \" -3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Betamethasone-17-valerate\\n\",\n        \"output\": \" -4.71\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][S][P][=Branch1][C][=O][Branch1][=Branch1][S][C][C][C][C][S][C][C][C][C]\\n\",\n        \"output\": \" DEF\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCC(C)C\\n\",\n        \"output\": \" 2-Methylheptane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Chloropentane\\n\",\n        \"output\": \" InChI=1S/C5H11Cl/c1-2-3-4-5-6/h2-5H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccc(Cl)cc1\\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1(O)c(C)ccc(C(C)C)c1\\n\",\n        \"output\": \" Carvacrol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H15ClNO4PS2/c1-3-16-19(20,17-4-2)21-8-14-10-6-5-9(13)7-11(10)18-12(14)15/h5-7H,3-4,8H2,1-2H3\\n\",\n        \"output\": \" -5.233\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C22H12/c1-3-13-7-9-15-11-12-16-10-8-14-4-2-6-18-17(5-1)19(13)21(15)22(16)20(14)18/h1-12H\\n\",\n        \"output\": \" -9.017999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccccc1\\n\",\n        \"output\": \" 0.025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Iodoheptane\\n\",\n        \"output\": \" CCCCCCCI\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H12/c1-3-5-7-6-4-2/h1H,4-7H2,2H3\\n\",\n        \"output\": \" -3.01\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,4-Dimethyl-2-pentanol \\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCBr\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 4.5708818961487516e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Chlorohexane\\n\",\n        \"output\": \" CCCCCCCl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Perfluidone\\n\",\n        \"output\": \" [C][C][=C][C][=Branch2][Ring1][=Branch1][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Azintamide\\n\",\n        \"output\": \" InChI=1S/C10H14ClN3OS/c1-3-14(4-2)10(15)7-16-9-6-5-8(11)12-13-9/h5-6H,3-4,7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cyclopentyl-5-spirobarbituric acid\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][N]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Griseofulvin\\n\",\n        \"output\": \" InChI=1S/C17H17ClO6/c1-8-5-9(19)6-12(23-4)17(8)16(20)13-10(21-2)7-11(22-3)14(18)15(13)24-17/h6-8H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" C1CCCC1\\n\",\n        \"output\": \" -2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][C][C][N][Ring1][Branch1]\\n\",\n        \"output\": \" 2-pyrrolidone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Prasterone\\n\",\n        \"output\": \" InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Brc1cccc(Br)c1\\n\",\n        \"output\": \" 1,3-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\\n\",\n        \"output\": \" -6.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CC(C)C(O)C(C)C\\n\",\n        \"output\": \" 0.06025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][S][=Branch1][C][=O][S][C][C][=C]\\n\",\n        \"output\": \" allicin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.18620871366628675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H6ClN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][=C]\\n\",\n        \"output\": \" 0.01148153621496883 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCc1ccc2ccccc2c1\\n\",\n        \"output\": \" 5.128613839913648e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 2,2,4,6,6'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1ccc(Cl)cc1C(=O)Nc2ccc(cc2Cl)N(=O)=O\\n\",\n        \"output\": \" Niclosamide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Quintozene\\n\",\n        \"output\": \" InChI=1S/C6Cl5NO2/c7-1-2(8)4(10)6(12(13)14)5(11)3(1)9\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCN(Cc1c(F)cccc1Cl)c2c(cc(cc2N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" 1.6595869074375596e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Butyne\\n\",\n        \"output\": \" [C][C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Isobutyl formate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][O][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h5,7,9,14-16,18,22,24,26H,3-4,6,8,10-11H2,1-2H3\\n\",\n        \"output\": \" Prednisolone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2,6-Dinitrotoluene\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" t-Butylbenzene \\n\",\n        \"output\": \" 0.00021877616239495518 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCOC(=O)C=Cc1ccccc1\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC(=O)N\\n\",\n        \"output\": \" O-Ethyl carbamate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 3,3-Dimethyl-2-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H15Cl3O2/c1-20-13-7-3-11(4-8-13)15(16(17,18)19)12-5-9-14(21-2)10-6-12/h3-10,15H,1-2H3\\n\",\n        \"output\": \" Methoxychlor\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" FC(F)(Cl)C(F)(F)Cl\\n\",\n        \"output\": \" -2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCC(=O)OCC\\n\",\n        \"output\": \" Ethyl heptanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C3H7Br/c1-3(2)4/h3H,1-2H3\\n\",\n        \"output\": \" 2-Bromopropane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC(C)CCO\\n\",\n        \"output\": \" 3-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H6O2/c1-3(4)5-2/h1-2H3\\n\",\n        \"output\": \" Methyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2Cl4/c3-1(4)2(5)6\\n\",\n        \"output\": \" Tetrachloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dulcin\\n\",\n        \"output\": \" InChI=1S/C9H12N2O2/c1-2-13-8-5-3-7(4-6-8)11-9(10)12/h3-6H,2H2,1H3,(H3,10,11,12)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" borneol\\n\",\n        \"output\": \" InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H5NO3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H12Cl2N2O/c18-14-7-5-12(6-8-14)17(22,13-9-20-11-21-10-13)15-3-1-2-4-16(15)19/h1-11,22H\\n\",\n        \"output\": \" Fenarimol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCc1c(C)nc(NCC)[nH]c1=O\\n\",\n        \"output\": \" -3.028\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H6N2OS/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)\\n\",\n        \"output\": \" methylthiouracil\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1,2,3-Trichlorobenzene\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCCCCO\\n\",\n        \"output\": \" 1-Dodecanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Octanoyloxymethylphenytoin\\n\",\n        \"output\": \" -6.523\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Octanoyloxymethylphenytoin\\n\",\n        \"output\": \" InChI=1S/C24H28N2O4/c1-2-3-4-5-12-17-21(27)30-18-26-22(28)24(25-23(26)29,19-13-8-6-9-14-19)20-15-10-7-11-16-20/h6-11,13-16H,2-5,12,17-18H2,1H3,(H,25,29)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.000630957344480193 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Isobutyl acetate\\n\",\n        \"output\": \" CC(C)COC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][O][C][C][C][C]\\n\",\n        \"output\": \" Dibutyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CH3Br/c1-2/h1H3\\n\",\n        \"output\": \" Bromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Glycerol\\n\",\n        \"output\": \" [O][C][C][Branch1][C][O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][=Branch2][Branch1][C][O][C][Branch1][C][O][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=Branch2][=O]\\n\",\n        \"output\": \" alloxantin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H12/c1-7-4-8(2)6-9(3)5-7/h4-6H,1-3H3\\n\",\n        \"output\": \" 1,3,5-Trimethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CNC(=O)Oc1cccc2ccccc12\\n\",\n        \"output\": \" -3.2239999999999998\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Propylisopropylether\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)(C)CCO\\n\",\n        \"output\": \" 3,3-Dimethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Nc1ccc(cc1)c2ccc(N)cc2\\n\",\n        \"output\": \" 0.001995262314968879 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCC(O)CCC\\n\",\n        \"output\": \" 0.039810717055349734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3-Octanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,1,1-Trichloroethane\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][=Branch2][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][C][Branch1][C][Cl][C][=Branch1][=N][=C][Branch1][C][Cl][C][=Branch1][Branch1][=C][Ring1][#Branch1][Cl][Cl][Cl]\\n\",\n        \"output\": \" Dienochlor\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" methylthiouracil\\n\",\n        \"output\": \" [C][C][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=S][NH1][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 4-Bromophenol\\n\",\n        \"output\": \" -1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Dodecanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-hexylresorcinol\\n\",\n        \"output\": \" [C][Branch1][C][O][=C][C][Branch1][C][O][=C][C][=C][Ring1][Branch2][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12N2O2/c18-13-15(17-14(19)16-13,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H2,16,17,18,19)\\n\",\n        \"output\": \" Phenytoin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H4N2/c1-2-5-4-6-3-1/h1-4H\\n\",\n        \"output\": \" Pyrimidine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H\\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Clc1ccc(c(Cl)c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" -7.92\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COC(=O)C=C\\n\",\n        \"output\": \" Methyl acrylate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Disulfoton\\n\",\n        \"output\": \" -4.23\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][Branch1][C][O][=C][Branch1][C][O][C][O][C][C][Branch1][C][O][C][C][=C][C][=Branch1][C][=O][C][Branch1][C][O][=C][C][Ring1][Branch2][=C][Ring1][N][C][=Ring1][S][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc1cc(cc(OC)c1O)C6C2C(COC2=O)C(OC4OC3COC(C)OC3C(O)C4O)c7cc5OCOc5cc67\\n\",\n        \"output\": \" Etoposide (148-167,25mg/ml)\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Nitroethane\\n\",\n        \"output\": \" InChI=1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Butanethiol \\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO\\n\",\n        \"output\": \" Dexamethasone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Methylcholanthrene\\n\",\n        \"output\": \" [C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][C][C][C][Branch1][=Branch1][C][Ring1][=Branch2][=Ring1][Branch1][=C][Ring1][N][C][=C][Ring1][S]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" DDT\\n\",\n        \"output\": \" -7.15\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][N][Branch1][=N][C][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.676\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Mirex\\n\",\n        \"output\": \" ClC1(C2(Cl)C3(Cl)C4(Cl)C5(Cl)C1(Cl)C3(Cl)Cl)C5(Cl)C(Cl)(Cl)C24Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cn2c(=O)on(c1ccc(Cl)c(Cl)c1)c2=O\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-6-4-2-3-5-7(6)8/h2-5,8H,1H3\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-5(2)4-6(3)7/h5-7H,4H2,1-3H3\\n\",\n        \"output\": \" 4-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)C\\n\",\n        \"output\": \" 5-Ethyl-5-isopropylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Hydrocortisone \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCOC(=O)c1ccccc1C(=O)OCC\\n\",\n        \"output\": \" 0.0044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-Methyl-2-pentanone\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-Heptanone\\n\",\n        \"output\": \" CCCC(=O)CCC\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dichlorophen\\n\",\n        \"output\": \" Oc1ccc(Cl)cc1Cc2cc(Cl)ccc2O\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Glycerol\\n\",\n        \"output\": \" OCC(O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1ccc2ccccc2c1\\n\",\n        \"output\": \" 0.005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2-Phenoxyethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Nitropropane\\n\",\n        \"output\": \" CCCN(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" glucose\\n\",\n        \"output\": \" InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Br][Br]\\n\",\n        \"output\": \" -1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propionitrile\\n\",\n        \"output\": \" CCC#N\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" Barbital\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\",\n        \"output\": \" Propazine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][S][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][C][C][C][Branch1][C][C][C][Branch1][#C][C][C][C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][O][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][Ring1][#C]\\n\",\n        \"output\": \" Spironolactone\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" m-Nitrophenol\\n\",\n        \"output\": \" InChI=1S/C6H5NO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][N][Branch1][O][C][O][C][=Branch1][C][=O][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.0989398836235246e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][Branch1][Ring1][C][C][C][C][C][C]\\n\",\n        \"output\": \" Di(2-ethylhexyl)-phthalate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1cc(cc(N(=O)=O)c1O)N(=O)=O\\n\",\n        \"output\": \" DNOC\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3\\n\",\n        \"output\": \" Testosterone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H12N2O3/c12-6-9(4-2-1-3-5-9)7(13)11-8(14)10-6/h1-5H2,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" 0.0008709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Heptane\\n\",\n        \"output\": \" InChI=1S/C7H16/c1-3-5-7-6-4-2/h3-7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][Branch1][C][Br][=C][C][Branch1][C][Br][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1,3,5-Tribromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][C][=Branch1][C][=O][O][C][C][Ring1][=Branch1][C][=Ring1][=C]\\n\",\n        \"output\": \" 0.012618275345906706 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CH3NO2/c1-2(3)4/h1H3\\n\",\n        \"output\": \" Nitromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Tetrabromomethane\\n\",\n        \"output\": \" BrC(Br)(Br)Br\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][N][C][=Branch1][C][=O][N][C][Branch1][Branch2][N][C][=Branch1][C][=O][O][C][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benomyl\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-3-5-4-2/h3H,1,4H2,2H3\\n\",\n        \"output\": \" Ethyl vinyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" p,p'-Biphenyldiamine \\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" L-arabinose\\n\",\n        \"output\": \" C1OC(O)C(O)C(O)C1O\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC34CCC1C(CC=C2CC(O)CCC12C)C3CCC4=O\\n\",\n        \"output\": \" 7.585775750291836e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Aniline \\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Chlorimuron-ethyl (ph 7)\\n\",\n        \"output\": \" CCOC(=O)c1ccccc1S(=O)(=O)NN(C=O)c2nc(Cl)cc(OC)n2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2\\n\",\n        \"output\": \" Glycerol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N]\\n\",\n        \"output\": \" 0.0009120108393559096 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" p-Nitroaniline\\n\",\n        \"output\": \" -2.37\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" N,N-Diethylaniline\\n\",\n        \"output\": \" CCN(CC)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -3.7960000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Carbaryl\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H\\n\",\n        \"output\": \" 4.466835921509635e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOC(=O)NCCOc2ccc(Oc1ccccc1)cc2\\n\",\n        \"output\": \" Fenoxycarb\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H10/c1-2-4-5-3-1/h1-5H2\\n\",\n        \"output\": \" Cyclopentane \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Chlortoluron\\n\",\n        \"output\": \" -3.483\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methoproptryne\\n\",\n        \"output\": \" COCCCNc1nc(NC(C)C)nc(SC)n1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-5(2)4-6(3)7/h5H,4H2,1-3H3\\n\",\n        \"output\": \" 4-Methyl-2-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Nc1ccc(O)cc1\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][O][C][C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N]\\n\",\n        \"output\": \" -2.928\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Progesterone\\n\",\n        \"output\": \" InChI=1S/C21H30O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12,16-19H,4-11H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1,2,3,4-Tetrahydronapthalene\\n\",\n        \"output\": \" -4.37\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-5(2)3-7-4-6/h4-5H,3H2,1-2H3\\n\",\n        \"output\": \" Isobutyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-2-3-7-10-8-5-4-6-9-10/h4-6,8-9H,2-3,7H2,1H3\\n\",\n        \"output\": \" 8.709635899560814e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Atratone\\n\",\n        \"output\": \" 0.008241381150130022 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Styrene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4ClNO2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H\\n\",\n        \"output\": \" m-Chloronitrobenzene \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-4-6(2)5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 2-Methylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-5-2-1-4(9)3-6(5)8/h1-3,9H\\n\",\n        \"output\": \" 0.05623413251903491 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\\n\",\n        \"output\": \" Ethyl-p-aminobenzoate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -3.65\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc2ncc1nccnc1n2\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-3-9-5-7-10(4-2)8-6-9/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" 0.00017782794100389227 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Pentyne\\n\",\n        \"output\": \" InChI=1S/C5H8/c1-3-5-4-2/h1H,4-5H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" ethyl cinnamate\\n\",\n        \"output\": \" InChI=1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Coumachlor\\n\",\n        \"output\": \" 1.4487718535447632e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Methyl-2-butanol\\n\",\n        \"output\": \" CC(C)C(C)O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3\\n\",\n        \"output\": \" 1.3182567385564074e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][O][C][C]\\n\",\n        \"output\": \" Ethyl propyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Bromonapthalene\\n\",\n        \"output\": \" -4.35\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Coronene\\n\",\n        \"output\": \" 4.6558609352295814e-10 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Piperophos\\n\",\n        \"output\": \" -4.15\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)c2ccccc2\\n\",\n        \"output\": \" p-Phenylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H7Cl/c1-3(2)4/h3H,1-2H3\\n\",\n        \"output\": \" 2-Chloropropane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2\\n\",\n        \"output\": \" 0.0008053784411990669 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Deltamethrin\\n\",\n        \"output\": \" 3.962780342554385e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Lorazepam\\n\",\n        \"output\": \" [O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][C][Ring2][Ring1][Ring1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2\\n\",\n        \"output\": \" Cyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" N-Methylaniline \\n\",\n        \"output\": \" CNc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,4-Dimethylnaphthalene \\n\",\n        \"output\": \" InChI=1S/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC1(C)C(C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2)C1(C)C\\n\",\n        \"output\": \" -6.025\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-benzidine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9)\\n\",\n        \"output\": \" -0.972\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3\\n\",\n        \"output\": \" -3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3/b3-2+\\n\",\n        \"output\": \" 2.0892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC1(C(=O)NC(=O)NC1=O)C2=CCC3CCC2C3\\n\",\n        \"output\": \" Reposal\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" linalool\\n\",\n        \"output\": \" InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2\\n\",\n        \"output\": \" 8.317637711026709e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3C(O)CC21C\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Chloroiodobenzene\\n\",\n        \"output\": \" Clc1ccc(I)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propyl acetate\\n\",\n        \"output\": \" InChI=1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H14NO4PS/c1-3-16-18(19,17-4-2)13-11(14)9-7-5-6-8-10(9)12(13)15/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" Ditalimfos\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H15NO2/c1-8(2)9-6-4-5-7-10(9)14-11(13)12-3/h4-8H,1-3H3,(H,12,13)\\n\",\n        \"output\": \" Isoprocarb\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H5NO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H\\n\",\n        \"output\": \" m-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCC(C)(C)O\\n\",\n        \"output\": \" 2-Methyl-2-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Atratone\\n\",\n        \"output\": \" CCNc1nc(NC(C)C)nc(OC)n1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" FC(F)(F)c1ccccc1\\n\",\n        \"output\": \" 0.003090295432513592 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][Ring2][C][C][=C][=C][C][=C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" -1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-10(2,3)9-7-5-4-6-8-9/h4-8H,1-3H3\\n\",\n        \"output\": \" t-Butylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H10O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,13H\\n\",\n        \"output\": \" 0.0003311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,1,2,2-Tetrachloroethane\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H22O2/c1-3-5-6-7-8-9-10-11(12)13-4-2/h3-10H2,1-2H3\\n\",\n        \"output\": \" Ethyl nonanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H14/c1-3-7-15(8-4-1)17-11-13-18(14-12-17)16-9-5-2-6-10-16/h1-14H\\n\",\n        \"output\": \" p-terphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Nonyne \\n\",\n        \"output\": \" InChI=1S/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Ring2][C][=Branch1][C][=O][C][O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Mefenacet\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 4.466835921509635e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][Cl]\\n\",\n        \"output\": \" Metoxuron\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Napthol\\n\",\n        \"output\": \" Oc1ccc2ccccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Thiourea\\n\",\n        \"output\": \" 2.0892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethylene\\n\",\n        \"output\": \" C=C\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" hydrobenzoin\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" draw\\n\",\n        \"output\": \" draw does not have SELFIES\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H14N4O4/c1-12-8-7(9(17)13(2)10(12)18)14(5-11-8)3-6(16)4-15/h5-6,15-16H,3-4H2,1-2H3\\n\",\n        \"output\": \" -0.17\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Androstenedione\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3,5-Dimethylphenol\\n\",\n        \"output\": \" InChI=1S/C8H10O/c1-6-3-7(2)5-8(9)4-6/h3-5,9H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Napthacene\\n\",\n        \"output\": \" InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H12N2O/c1-11(2)9(12)10-8-6-4-3-5-7-8/h3-7H,1-2H3,(H,10,12)\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" COc1cc(CC=C)ccc1O\\n\",\n        \"output\": \" -1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" OCC1OC(O)(CO)C(O)C1O\\n\",\n        \"output\": \" Fructose\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H\\n\",\n        \"output\": \" 2-Napthol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dibromomethane\\n\",\n        \"output\": \" BrCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" p-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Heptene\\n\",\n        \"output\": \" 0.00018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" m-Chlorobromobenzene\\n\",\n        \"output\": \" Clc1cccc(Br)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Carbophenthion\\n\",\n        \"output\": \" CCOP(=S)(OCC)SCSc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 5,6-Dimethylchrysene\\n\",\n        \"output\": \" InChI=1S/C20H16/c1-13-14(2)20-17-9-4-3-7-15(17)11-12-19(20)18-10-6-5-8-16(13)18/h3-12H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCOC=O\\n\",\n        \"output\": \" 1.4125375446227544 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Tetrachloromethane\\n\",\n        \"output\": \" ClC(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,2',3,4,5,5'-PCB\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][C][=C][C][=C][C][=C][C][=C][C][Branch1][=N][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=Ring1][=N][=C][Ring1][=Branch2][Ring1][=N]\\n\",\n        \"output\": \" 1.5703628043335515e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzyltrifluoride\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-5-4-8-15-13(11)10-9-12-6-2-3-7-14(12)15/h2-10H,1H3\\n\",\n        \"output\": \" 1-Methylphenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1-Napthol\\n\",\n        \"output\": \" -2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Oc1cc(Cl)cc(Cl)c1\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)\\n\",\n        \"output\": \" Chloramphenicol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,3-Difluorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4F2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Bromotoluene\\n\",\n        \"output\": \" InChI=1S/C7H7Br/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-3-5(6)4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" 0.5248074602497725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 3,5-Dichlorophenol\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" trans-1,4-Dimethylcyclohexane\\n\",\n        \"output\": \" [C][/C][C][C][C][Branch1][C][\\\\C][C][C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ethyl pentanoate\\n\",\n        \"output\": \" InChI=1S/C7H14O2/c1-3-5-7(8)9-6-4-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H9ClF3N3O/c1-17-9-6-18-19(11(20)10(9)13)8-4-2-3-7(5-8)12(14,15)16/h2-6,17H,1H3\\n\",\n        \"output\": \" norflurazon\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)C)CC=C\\n\",\n        \"output\": \" 5-Allyl-5-isopropylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2\\n\",\n        \"output\": \" Acenapthene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Piperine\\n\",\n        \"output\": \" [O][=C][Branch2][Ring1][C][C][=C][C][=C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=O)OCC(COC(=O)C)OC(=O)C\\n\",\n        \"output\": \" Glyceryl triacetate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCC(=O)OCC\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Acetanilide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Decanol\\n\",\n        \"output\": \" InChI=1S/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-6(3,7)5-2/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.436515832240166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Methyl propionate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" cis 1,2-Dichloroethylene\\n\",\n        \"output\": \" [Cl][\\\\C][=C][/Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H15Br/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=O]\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" -2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H5Cl/c1-2-3/h2H2,1H3\\n\",\n        \"output\": \" 0.08709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCCCO\\n\",\n        \"output\": \" 3.981071705534969e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H14O6/c1-6(10)13-4-9(15-8(3)12)5-14-7(2)11/h9H,4-5H2,1-3H3\\n\",\n        \"output\": \" Glyceryl triacetate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Sulfanilamide\\n\",\n        \"output\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10Cl12/c11-1-2(12)7(17)4(14)3(13,5(1,15)9(7,19)20)6(1,16)10(21,22)8(2,4)18\\n\",\n        \"output\": \" Mirex\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][Cl][C][Cl]\\n\",\n        \"output\": \" 1,2-Dichloropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC34CCC1C(=CCc2cc(O)ccc12)C3CCC4=O\\n\",\n        \"output\": \" -5.282\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cccc(C)n1\\n\",\n        \"output\": \" 2,6-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Cc1ccc(Br)cc1\\n\",\n        \"output\": \" 0.0006456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4F2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\",\n        \"output\": \" 1,4-Difluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H16Cl2N2O/c1-3-4-7-16(2)12(17)15-9-5-6-10(13)11(14)8-9/h5-6,8H,3-4,7H2,1-2H3,(H,15,17)\\n\",\n        \"output\": \" 1.698243652461746e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCC(C)(O)CC\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2-Benzenediol\\n\",\n        \"output\": \" Oc1ccccc1O\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1ccc(c(Cl)c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" 2,2',3,4,4',5',6-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Diallate\\n\",\n        \"output\": \" InChI=1S/C10H17Cl2NOS/c1-7(2)13(8(3)4)10(14)15-6-9(12)5-11/h5,7-8H,6H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][=C]\\n\",\n        \"output\": \" 1-Hexene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCN(CC)C(=O)CSc1ccc(Cl)nn1\\n\",\n        \"output\": \" Azintamide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Perylene\\n\",\n        \"output\": \" InChI=1S/C20H12/c1-5-13-6-2-11-17-18-12-4-8-14-7-3-10-16(20(14)18)15(9-1)19(13)17/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Phosalone\\n\",\n        \"output\": \" CCOP(=S)(OCC)SCn1c(=O)oc2cc(Cl)ccc12\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Chlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Chloroanisole\\n\",\n        \"output\": \" -2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" -4.14\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H24NO4PS/c1-6-18-21(22,16-11(2)3)20-14-10-8-7-9-13(14)15(17)19-12(4)5/h7-12H,6H2,1-5H3,(H,16,22)\\n\",\n        \"output\": \" Isofenphos\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methyl-1-Pentene\\n\",\n        \"output\": \" CCCC(=C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" -2.64\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,4-Dimethylphenol\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethyl acetate\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67\\n\",\n        \"output\": \" Coronene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H8/c1-2-4-6-5-3-1/h1-2,5-6H,3-4H2\\n\",\n        \"output\": \" -2.06\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Griseofulvin\\n\",\n        \"output\": \" [C][O][C][=C][C][=Branch1][C][=O][C][C][Branch1][C][C][C][Ring1][Branch2][O][C][=C][Branch1][C][Cl][C][Branch1][Ring1][O][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][O][C][Ring1][=C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Cc1ccc(cc1N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CON(C)C(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" Monolinuron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-7(2)5-8-4-6/h3-5H,1-2H3\\n\",\n        \"output\": \" 3,5-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Clomazone\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][O][N][Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][Ring1][=C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Propanil\\n\",\n        \"output\": \" 0.001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Carbaryl\\n\",\n        \"output\": \" InChI=1S/C12H11NO2/c1-13-12(14)15-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3,(H,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-t-Butylphenol\\n\",\n        \"output\": \" InChI=1S/C10H14O/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H7NO/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2\\n\",\n        \"output\": \" -0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" c1cnc2c(c1)ccc3ncccc23\\n\",\n        \"output\": \" 0.0020892961308540386 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-5-6(7)4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Diazepam\\n\",\n        \"output\": \" 0.0001761976046411631 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.62\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][C][Branch1][C][C][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Dexamethasone\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Quinoline\\n\",\n        \"output\": \" InChI=1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][N][N][=C][C][Branch1][C][N][=C][Branch1][C][Br][C][Ring1][Branch2][=O]\\n\",\n        \"output\": \" brompyrazone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Cresol\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Br]\\n\",\n        \"output\": \" 1-Bromo-2-methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)\\n\",\n        \"output\": \" Inosine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Brc1cccc2ccccc12\\n\",\n        \"output\": \" -4.35\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H4N4/c3-2-4-1-5-6-2/h1H,(H3,3,4,5,6)\\n\",\n        \"output\": \" 3.326595532940045 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dimethoxymethane\\n\",\n        \"output\": \" InChI=1S/C3H8O2/c1-4-3-5-2/h3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C23H26N2O4/c1-2-3-4-11-16-20(26)29-17-25-21(27)23(24-22(25)28,18-12-7-5-8-13-18)19-14-9-6-10-15-19/h5-10,12-15H,2-4,11,16-17H2,1H3,(H,24,28)\\n\",\n        \"output\": \" 5.000345349769783e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(C)CCO\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Bromopropane\\n\",\n        \"output\": \" [C][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" COP(=O)(OC)OC(=CCl)c1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" -4.522\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)\\n\",\n        \"output\": \" 4.2072662838444376e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Chlorobiphenyl\\n\",\n        \"output\": \" c1c(Cl)cccc1c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][=Branch2][C][=C][N][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" Fenarimol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 3-Pentanol\\n\",\n        \"output\": \" -0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Simetryn\\n\",\n        \"output\": \" 0.002108628149933289 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H13ClN2O2/c1-5-6(10)7(13)12(8(14)11-5)9(2,3)4/h1-4H3,(H,11,14)\\n\",\n        \"output\": \" -2.484\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Epiandrosterone\\n\",\n        \"output\": \" InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2-Hexanone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1N(C2CCC(=O)NC2=O)C(=O)c3ccccc13\\n\",\n        \"output\": \" Thalidomide\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,3-Dimethylnaphthalene\\n\",\n        \"output\": \" InChI=1S/C12H12/c1-9-7-11-5-3-4-6-12(11)8-10(9)2/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Acenapthene\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Methyl nonanoate\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Amitrole\\n\",\n        \"output\": \" 0.522\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCBr\\n\",\n        \"output\": \" 1-Bromohexane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" thioanisole\\n\",\n        \"output\": \" InChI=1S/C7H8S/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1CC=CC1\\n\",\n        \"output\": \" Cyclopentene \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C]\\n\",\n        \"output\": \" Butane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C3H4O/c1-2-3-4/h2-3H,1H2\\n\",\n        \"output\": \" 3.715352290971725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 0.000707945784384138 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCC\\n\",\n        \"output\": \" -3.84\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Atratone\\n\",\n        \"output\": \" [C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][N]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC(=O)N(C)C(=O)CSP(=S)(OCC)OCC\\n\",\n        \"output\": \" -2.5180000000000002\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Acenapthene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pyrene\\n\",\n        \"output\": \" InChI=1S/C16H10/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)Nc1cccc(c1)C(F)(F)F\\n\",\n        \"output\": \" Fluometuron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Br][C][Branch1][C][Br][Branch1][C][Br][Br]\\n\",\n        \"output\": \" Tetrabromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Hexamethylbenzene\\n\",\n        \"output\": \" 5.888436553555884e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCC(=O)OC\\n\",\n        \"output\": \" Methyl nonanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=Branch1][C][=S][N]\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H20N2O/c1-11-7-5-6-10-13(11)16-14(17)15-12-8-3-2-4-9-12/h2-4,8-9,11,13H,5-7,10H2,1H3,(H2,15,16,17)\\n\",\n        \"output\": \" -4.11\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 4-Isopropyltoluene\\n\",\n        \"output\": \" -3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 7,12-Dimethylbenz(a)anthracene\\n\",\n        \"output\": \" 9.549925860214369e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Nonane\\n\",\n        \"output\": \" CCCCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 6.668067692136218e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Pentylbenzene\\n\",\n        \"output\": \" 2.290867652767775e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Ethyl vinyl ether\\n\",\n        \"output\": \" CCOC=C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][Ring1][C][O][Branch2][Ring2][#Branch2][O][C][O][C][Branch2][Ring1][=Branch1][C][O][C][O][C][Branch1][Ring1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Branch1][O][C][Branch1][C][O][C][Ring2][Ring1][#C][O]\\n\",\n        \"output\": \" Raffinose\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Salicin\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][=C][C][=C][O][Ring1][Branch1]\\n\",\n        \"output\": \" Furfural\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CHCl3/c2-1(3)4/h1H\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,2-Propylene oxide\\n\",\n        \"output\": \" CC1CO1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Heptanol \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H14O/c1-3-5-6-8(4-2)7-9/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 2-Ethyl-2-hexanal\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H\\n\",\n        \"output\": \" Carbazole\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-6-7-14-9-12-4-2-3-5-13(12)10-15(14)8-11/h2-10H,1H3\\n\",\n        \"output\": \" -6.96\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" -1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][Branch1][N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][#C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Hexanoyloxymethylphenyltoin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 9-Methylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-5(7)6(2,3)4/h1-4H3\\n\",\n        \"output\": \" -0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,4-Dibromobenzene\\n\",\n        \"output\": \" [Br][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" 0.0004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4ClI/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" o-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Ethylbutanal\\n\",\n        \"output\": \" [C][C][C][Branch1][Ring1][C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Ethyl-1-butanol\\n\",\n        \"output\": \" [C][C][C][Branch1][Ring1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Danazol\\n\",\n        \"output\": \" CC23Cc1cnoc1C=C2CCC4C3CCC5(C)C4CCC5(O)C#C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3\\n\",\n        \"output\": \" -7.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylheptane\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Diethyldisulfide\\n\",\n        \"output\": \" InChI=1S/C4H10S2/c1-3-5-6-4-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" OCc1ccccc1\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][C][C][Branch1][C][Cl][=C]\\n\",\n        \"output\": \" 0.0004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethylcyclohexane\\n\",\n        \"output\": \" InChI=1S/C8H16/c1-2-8-6-4-3-5-7-8/h8H,2-7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H5N3O6/c1-4-6(9(13)14)2-5(8(11)12)3-7(4)10(15)16/h2-3H,1H3\\n\",\n        \"output\": \" 2,4,6-Trinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/CHBr3/c2-1(3)4/h1H\\n\",\n        \"output\": \" 0.012302687708123818 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H12N4O3/c17-11(14-8-10-4-2-1-3-5-10)9-15-7-6-13-12(15)16(18)19/h1-7H,8-9H2,(H,14,17)\\n\",\n        \"output\": \" -2.81\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Chlorthalidone\\n\",\n        \"output\": \" InChI=1S/C14H11ClN2O4S/c15-11-6-5-8(7-12(11)22(16,20)21)14(19)10-4-2-1-3-9(10)13(18)17-14/h1-7,19H,(H,17,18)(H2,16,20,21)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Clomazone\\n\",\n        \"output\": \" 0.004591980128368685 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 5-Allyl-5-isopropylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H13Br/c1-2-3-4-5-6-7/h2-6H2,1H3\\n\",\n        \"output\": \" 1-Bromohexane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H18/c1-2-3-4-6-9-12-10-7-5-8-11-12/h5,7-8,10-11H,2-4,6,9H2,1H3\\n\",\n        \"output\": \" Hexylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Chloropham\\n\",\n        \"output\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Heptyne\\n\",\n        \"output\": \" CCCCCC#C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H13ClN2/c1-8-6-9(11)4-5-10(8)12-7-13(2)3/h4-7H,1-3H3\\n\",\n        \"output\": \" chlordimeform\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H18N6/c1-13(2)7-10-8(14(3)4)12-9(11-7)15(5)6/h1-6H3\\n\",\n        \"output\": \" Altretamine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Ipazine\\n\",\n        \"output\": \" -3.785\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Methyl butyl ether \\n\",\n        \"output\": \" -0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1=Cc2cccc3cccc1c23\\n\",\n        \"output\": \" Acenapthylene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" C=CC=C\\n\",\n        \"output\": \" 0.013489628825916533 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Prometryn\\n\",\n        \"output\": \" -4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Napthol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Isonazid\\n\",\n        \"output\": \" [C][=N][C][=C][C][Branch1][#Branch1][C][=Branch1][C][=O][N][N][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=C][C][Ring1][Branch1][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.4125375446227554e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Nimetazepam\\n\",\n        \"output\": \" CN2C(=O)CN=C(c1ccccc1)c3cc(ccc23)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC1(CCC(C)C)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" Amobarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1(O)cc(O)ccc1CCCCCC\\n\",\n        \"output\": \" -2.59\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Glafenine\\n\",\n        \"output\": \" [O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCNc1nc(Cl)nc(NC(C)C)n1\\n\",\n        \"output\": \" -3.85\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Fenpropathrin\\n\",\n        \"output\": \" CC1(C)C(C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2)C1(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H11Cl/c1-2-3-4-5-6/h2-5H2,1H3\\n\",\n        \"output\": \" -2.73\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2\\n\",\n        \"output\": \" Cyclohexene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 1,2-Dinitrobenzene\\n\",\n        \"output\": \" 0.0007943282347242813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" 1-Bromonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 1-Chlorohexane\\n\",\n        \"output\": \" 0.0007585775750291836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" D-fenchone\\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Phenetole\\n\",\n        \"output\": \" InChI=1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][P][Ring1][#Branch2]\\n\",\n        \"output\": \" -8.04\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][P][C][Branch1][Ring1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Hexestrol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cyclooctanol\\n\",\n        \"output\": \" OC1CCCCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Indan\\n\",\n        \"output\": \" 0.0009120108393559096 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3\\n\",\n        \"output\": \" 1-Butanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-4-5-6(2)3/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" 2-Methylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-Pentene-1-ol\\n\",\n        \"output\": \" OCCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Eriodictyol\\n\",\n        \"output\": \" InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(=O)OCC(COC(=O)C)OC(=O)C\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h5,7,9,14-16,18,22,24,26H,3-4,6,8,10-11H2,1-2H3\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][I]\\n\",\n        \"output\": \" -2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Benzyltrifluoride\\n\",\n        \"output\": \" 0.003090295432513592 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COc2cnc1ncncc1n2\\n\",\n        \"output\": \" 6-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Benzotriazole\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-8(2)10-7-5-4-6-9(10)3/h4-8H,1-3H3\\n\",\n        \"output\": \" -3.76\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" o-Fluorobromobenzene\\n\",\n        \"output\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Heptanoyloxymethylphenytoin\\n\",\n        \"output\": \" O=C1N(COC(=O)CCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1CCCC1\\n\",\n        \"output\": \" Cyclopentane \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" o-Aminophenol\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" methylthiouracil\\n\",\n        \"output\": \" InChI=1S/C5H6N2OS/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Butethal\\n\",\n        \"output\": \" CCCCC1(CC)C(=O)NC(=O)NC1=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCNC(=O)n1c(NC(=O)OC)nc2ccccc12\\n\",\n        \"output\": \" Benomyl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 1,3,5-Trinitrobenzene\\n\",\n        \"output\": \" 0.0012882495516931337 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H7Cl/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\\n\",\n        \"output\": \" 4-Chlorotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Propyl formate\\n\",\n        \"output\": \" CCCOC=O\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" COC(=O)c1ccccc1C(=O)OC\\n\",\n        \"output\": \" -1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H8Cl2IO3PS/c1-12-15(16,13-2)14-8-4-5(9)7(11)3-6(8)10/h3-4H,1-2H3\\n\",\n        \"output\": \" 2.39883291901949e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its oil solubility. ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][N]\\n\",\n        \"output\": \" Methyl hydrazine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Bendroflumethiazide\\n\",\n        \"output\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch1][N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][Ring1][=N][=Branch1][C][=O][=O][C][=C][Ring2][Ring1][Ring1][C][Branch1][C][F][Branch1][C][F][F]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" Monuron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][S][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][C][C][C][Branch1][C][C][C][Branch1][#C][C][C][C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][O][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][Ring1][#C]\\n\",\n        \"output\": \" -4.173\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ncc(N(=O)=O)n1CCO\\n\",\n        \"output\": \" -1.22\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pentyl propanoate\\n\",\n        \"output\": \" InChI=1S/C7H14O2/c1-3-5-6-7(8)9-4-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Fenuron\\n\",\n        \"output\": \" 0.025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3,4-Dichloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCC(O)CC\\n\",\n        \"output\": \" 3-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C3H4/c1-3-2/h1H,2H3\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Fluridone\\n\",\n        \"output\": \" InChI=1S/C19H14F3NO/c1-23-11-16(13-6-3-2-4-7-13)18(24)17(12-23)14-8-5-9-15(10-14)19(20,21)22/h2-12H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Vinclozolin\\n\",\n        \"output\": \" 1.188502227437019e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Diethyldisulfide\\n\",\n        \"output\": \" [C][C][S][S][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" c1(C(=O)OCCCCCC(C)(C))c(C(=O)OCCCCCC(C)(C))cccc1\\n\",\n        \"output\": \" -6.6370000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CON(C)C(=O)Nc1ccc(Br)c(Cl)c1\\n\",\n        \"output\": \" 0.0001191242008027375 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" Phosalone\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,4-Dichlorophenol \\n\",\n        \"output\": \" InChI=1S/C6H4Cl2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dimethyldisulfide\\n\",\n        \"output\": \" CSSC\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/CH4O/c1-2/h2H,1H3\\n\",\n        \"output\": \" 37.15352290971726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3,4-Dichlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H15O2PS3/c1-4-11-5-6-12-9(10,7-2)8-3/h4-6H2,1-3H3\\n\",\n        \"output\": \" Thiometon\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H15Cl/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCC\\n\",\n        \"output\": \" Hexane \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-4-5-6-9-7(2)8/h3-6H2,1-2H3\\n\",\n        \"output\": \" 0.012882495516931342 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" BrC(Br)Br\\n\",\n        \"output\": \" Tribromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-3-5-8-6(7)4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Chloropentane\\n\",\n        \"output\": \" [C][C][C][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dimethyldisulfide\\n\",\n        \"output\": \" InChI=1S/C2H6S2/c1-3-4-2/h1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" t-Butylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Methylparaben\\n\",\n        \"output\": \" 0.014893610777109155 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ametryn\\n\",\n        \"output\": \" CCNc1nc(NC(C)C)nc(SC)n1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" ClC(Cl)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" 0.0025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Chlordane\\n\",\n        \"output\": \" -6.86\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.0007943282347242813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=O]\\n\",\n        \"output\": \" 2-butenal\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H4Cl6/c13-5-1-2-8(14)6(3-5)7-4-9(15)11(17)12(18)10(7)16/h1-4H\\n\",\n        \"output\": \" 2,2',3,4,5,5'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H5N3O6/c1-4-6(9(13)14)2-5(8(11)12)3-7(4)10(15)16/h2-3H,1H3\\n\",\n        \"output\": \" 0.0006025595860743575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" Pentylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)C(c2ccc(Cl)cc2)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" DDT\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=C2NC(=O)C1(CCCCC1)C(=O)N2\\n\",\n        \"output\": \" -3.06\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,2,5-Trimethylhexane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(=C)C1CC=C(C)C(=O)C1\\n\",\n        \"output\": \" 0.008709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H8ClN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\\n\",\n        \"output\": \" Pyrazon\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benzocaine\\n\",\n        \"output\": \" InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2-Dichloroethane\\n\",\n        \"output\": \" [Cl][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-5-7(4)6(2)3/h6-7H,5H2,1-4H3\\n\",\n        \"output\": \" -4.28\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fenfuram\\n\",\n        \"output\": \" [C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Triphenylene\\n\",\n        \"output\": \" 1.8793168168032686e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" Methyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Urea\\n\",\n        \"output\": \" NC(=O)N\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-6-9-15-13(10-11)8-7-12-4-2-3-5-14(12)15/h2-10H,1H3\\n\",\n        \"output\": \" -5.84\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Methyl-3-heptanol\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(=O)C\\n\",\n        \"output\": \" 2-Pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][C][Ring1][=C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" Napthacene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1,2-Propylene oxide\\n\",\n        \"output\": \" 0.2570395782768864 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc2ccc1oc(=O)[nH]c1c2\\n\",\n        \"output\": \" Chlorzoxazone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCC1CCCC1\\n\",\n        \"output\": \" Pentylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C]\\n\",\n        \"output\": \" -2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CON(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" -3.592\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H17Cl2N3O2/c1-2-3-12-7-21-15(22-12,8-20-10-18-9-19-20)13-5-4-11(16)6-14(13)17/h4-6,9-10,12H,2-3,7-8H2,1H3\\n\",\n        \"output\": \" Propiconazole\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,3,5-Trimethylbenzene \\n\",\n        \"output\": \" InChI=1S/C9H12/c1-7-4-8(2)6-9(3)5-7/h4-6H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Nitrapyrin\\n\",\n        \"output\": \" InChI=1S/C6H3Cl4N/c7-5-3-1-2-4(11-5)6(8,9)10/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cc(ccc1NS(=O)(=O)C(F)(F)F)S(=O)(=O)c2ccccc2\\n\",\n        \"output\": \" Perfluidone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1(C(=O)OCCCCCC(C)(C))c(C(=O)OCCCCCC(C)(C))cccc1\\n\",\n        \"output\": \" diisooctyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1c(Cl)c(Cl)cc(Cl)c1Cl\\n\",\n        \"output\": \" 2,3,5,6-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Xylene \\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Oc1ccccc1O\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H9NO/c1-4(6)5(2)3/h1-3H3\\n\",\n        \"output\": \" 12.882495516931343 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H12/c1-4-5-6(2)3/h2,4-5H2,1,3H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.6919999999999997\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Diosgenin\\n\",\n        \"output\": \" C1C(O)CCC2(C)CC3CCC4(C)C5(C)CC6OCC(C)CC6OC5CC4C3C=C21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-5-6(7)4-2/h4,6-7H,2-3,5H2,1H3\\n\",\n        \"output\": \" 1-Hexene-3-ol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11NO2/c1-13-12(14)15-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3,(H,13,14)\\n\",\n        \"output\": \" Carbaryl\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H19N3O5S2/c1-8-10(12(19)16-13(20)14-8)3-4-11(18)15-9(5-17)6-23(21)7-22-2/h3-4,9,17H,5-7H2,1-2H3,(H,15,18)(H2,14,16,19,20)\\n\",\n        \"output\": \" 0.010447202192208004 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Amitraz\\n\",\n        \"output\": \" 3.3884415613920275e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" Dinitramine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H11Cl/c1-4-5(2,3)6/h4H2,1-3H3\\n\",\n        \"output\": \" -2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClC(=C)Cl\\n\",\n        \"output\": \" 1,1-Dichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C\\n\",\n        \"output\": \" Methane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0009120108393559096 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][#Branch1][C][=C][Ring1][O]\\n\",\n        \"output\": \" phthalamide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OC1CCCCCC1\\n\",\n        \"output\": \" Cycloheptanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H16/c1-2-3-5-8-11-9-6-4-7-10-11/h4,6-7,9-10H,2-3,5,8H2,1H3\\n\",\n        \"output\": \" -4.64\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" citral\\n\",\n        \"output\": \" -2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Cl]\\n\",\n        \"output\": \" 2-Chloropropane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" 3,4-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Bromodichloromethane\\n\",\n        \"output\": \" InChI=1S/CHBrCl2/c2-1(3)4/h1H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Indan\\n\",\n        \"output\": \" C1Cc2ccccc2C1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-2-4-5-3-1/h1-5H2\\n\",\n        \"output\": \" 0.0022908676527677724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-methyluracil\\n\",\n        \"output\": \" InChI=1S/C5H6N2O2/c1-7-3-2-4(8)6-5(7)9/h2-3H,1H3,(H,6,8,9)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC2(C)C1CCC(C)(C1)C2=O\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC\\n\",\n        \"output\": \" Malathion\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Isobutylbenzene\\n\",\n        \"output\": \" CC(C)Cc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Chlorzoxazone\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][O][C][=Branch1][C][=O][NH1][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Triamterene\\n\",\n        \"output\": \" -2.404\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H18/c1-3-5-7-8-6-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" -5.24\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][N]\\n\",\n        \"output\": \" 21.87761623949553 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Quinethazone\\n\",\n        \"output\": \" CCC2NC(=O)c1cc(c(Cl)cc1N2)S(N)(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-3-5-6(7)8-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" Methyl pentanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1cncnc1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 2-Heptanol \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-5-7-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" Dipropyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H\\n\",\n        \"output\": \" 1e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2.691534803926914e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1,3-diethylthiourea\\n\",\n        \"output\": \" -1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,4-Dichlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4Cl2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Butylate\\n\",\n        \"output\": \" InChI=1S/C11H23NOS/c1-6-14-11(13)12(7-9(2)3)8-10(4)5/h9-10H,6-8H2,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" COc1ccc(C=CC)cc1\\n\",\n        \"output\": \" -3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2H2Cl4/c3-1(4)2(5)6/h1-2H\\n\",\n        \"output\": \" 0.018197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1c(Cl)cc(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" 2,3,4,6-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Methyl-2-pentanone\\n\",\n        \"output\": \" CCC(C)C(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H16N2O2/c1-3-18-14(17)13-9-15-10-16(13)11(2)12-7-5-4-6-8-12/h4-11H,3H2,1-2H3\\n\",\n        \"output\": \" Etomidate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Methyl-1-Butene\\n\",\n        \"output\": \" InChI=1S/C5H10/c1-4-5(2)3/h2,4H2,1,3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -7.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,3,4,6-Tetrachlorophenol\\n\",\n        \"output\": \" [O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][O][C][Branch1][C][C][C][S][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Bensulide\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][Cl]\\n\",\n        \"output\": \" -2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" DDE\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethyl propionate\\n\",\n        \"output\": \" CCOC(=O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" o-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2-Dibromoethane\\n\",\n        \"output\": \" BrCCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H22N2O/c1-15(2)13(16)14-12-7-8-6-11(12)10-5-3-4-9(8)10/h8-12H,3-7H2,1-2H3,(H,14,16)\\n\",\n        \"output\": \" Norea\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][P][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Nitrazepam\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Hydrocortisone 21-acetate\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][O][C][C][=Branch1][C][=O][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][Branch1][C][O][C][C][Ring1][P][Ring2][Ring1][Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C]\\n\",\n        \"output\": \" 5-Allyl-5-ethylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" 1,2,4,5-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" -5.16\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Pentanoyloxymethylphenytoin\\n\",\n        \"output\": \" [O][=C][N][Branch1][O][C][O][C][=Branch1][C][=O][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H23F2NO4/c1-17(2)24(18-11-13-21(14-12-18)32-26(27)28)25(30)33-23(16-29)19-7-6-10-22(15-19)31-20-8-4-3-5-9-20/h3-15,17,23-24,26H,1-2H3\\n\",\n        \"output\": \" Flucythrinate\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Cyfluthrin\\n\",\n        \"output\": \" InChI=1S/C22H18Cl2FNO3/c1-22(2)15(11-19(23)24)20(22)21(27)29-18(12-26)13-8-9-16(25)17(10-13)28-14-6-4-3-5-7-14/h3-11,15,18,20H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,3,5-Trimethylbenzene \\n\",\n        \"output\": \" 0.00039810717055349735 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)C(=O)C(C)C\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc1ccccc1\\n\",\n        \"output\": \" Anisole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)Br\\n\",\n        \"output\": \" 2-Bromopropane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" trans-2-Pentene \\n\",\n        \"output\": \" [C][C][/C][=C][/C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-3-5-6-7(8)4-2/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 0.033884415613920256 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" ethyl cinnamate\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Br][C][=C][C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Br]\\n\",\n        \"output\": \" -6.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" Ditalimfos\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" OC(Cn1cncn1)(c2ccc(F)cc2)c3ccccc3F\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Quinoline\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-7-4-5-8(2)9(3)6-7/h4-6H,1-3H3\\n\",\n        \"output\": \" 0.0004897788193684461 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc2ccccc2c1\\n\",\n        \"output\": \" 2-Methylnapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0026915348039269166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methyl butyl ether \\n\",\n        \"output\": \" CCCCOC\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Dibenzofurane\\n\",\n        \"output\": \" InChI=1S/C12H8O/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Phenylethanol\\n\",\n        \"output\": \" CC(O)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1N(COC(=O)C)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3-Ethanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccc2c(c1)c3cccc4ccc5cccc2c5c43\\n\",\n        \"output\": \" -7.8\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Inosine\\n\",\n        \"output\": \" OCC1OC(C(O)C1O)n2cnc3c(O)ncnc23\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Nitropropane\\n\",\n        \"output\": \" InChI=1S/C3H7NO2/c1-2-3-4(5)6/h2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,3,4-Trichlorophenol\\n\",\n        \"output\": \" Oc1ccc(Cl)c(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3-Chloroanisole\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(cc1Cl)N(=O)=O\\n\",\n        \"output\": \" 4.897788193684466e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Flumetralin\\n\",\n        \"output\": \" InChI=1S/C16H12ClF4N3O4/c1-2-22(8-10-11(17)4-3-5-12(10)18)15-13(23(25)26)6-9(16(19,20)21)7-14(15)24(27)28/h3-7H,2,8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" Fluometuron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\",\n        \"output\": \" Ipazine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,1-Dichloroethane\\n\",\n        \"output\": \" InChI=1S/C2H4Cl2/c1-2(3)4/h2H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Corticosterone\\n\",\n        \"output\": \" CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Caffeine\\n\",\n        \"output\": \" 0.13304544179780914 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,3-Dimethylnaphthalene\\n\",\n        \"output\": \" Cc1cc2ccccc2cc1C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diazepam\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCCCC=C\\n\",\n        \"output\": \" -5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CC=C\\n\",\n        \"output\": \" 5-Allyl-5-ethylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" OCC(O)CO\\n\",\n        \"output\": \" 13.182567385564074 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Aldrin\\n\",\n        \"output\": \" 4.931738039549355e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][Cl]\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" Benzo(b)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propylcyclopentane\\n\",\n        \"output\": \" InChI=1S/C8H16/c1-2-5-8-6-3-4-7-8/h8H,2-7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCl\\n\",\n        \"output\": \" 1-Chloropropane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Phenanthrene\\n\",\n        \"output\": \" InChI=1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][I]\\n\",\n        \"output\": \" o-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Brc1ccc2ccccc2c1\\n\",\n        \"output\": \" 3.9810717055349695e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1cC2C(=O)NC(=O)C2cc1\\n\",\n        \"output\": \" phthalamide\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" freckle\\n\",\n        \"output\": \" freckle does not have SELFIES\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Bromoheptane\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" -4.66\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+\\n\",\n        \"output\": \" 0.00015135612484362088 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-7(2)5-8-4-6/h3-5H,1-2H3\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Methyl-2-pentanone\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-4-5(2)6(3)7/h5H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" difluron\\n\",\n        \"output\": \" [F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H28NO3PS2/c1-4-10-17-19(20,18-11-5-2)21-12-14(16)15-9-7-6-8-13(15)3/h13H,4-12H2,1-3H3\\n\",\n        \"output\": \" Piperophos\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Butabarbital\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC34CCC1C(CCC2=CC(=O)CCC12C)C3CCC4=O\\n\",\n        \"output\": \" Androstenedione\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2HCl5/c3-1(4)2(5,6)7/h1H\\n\",\n        \"output\": \" Pentachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2-Methylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" hematein\\n\",\n        \"output\": \" c1cc(O)c(O)c2OCC3(O)CC4=CC(=O)C(O)=CC4=C3c21\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Lindane\\n\",\n        \"output\": \" [Cl][C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H5N3/c1-2-4-6-5(3-1)7-9-8-6/h1-4H,(H,7,8,9)\\n\",\n        \"output\": \" Benzotriazole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-3-5-8-6(7)4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" Methyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4BrCl/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" -3.19\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" equinox\\n\",\n        \"output\": \" equinox does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Dibutyl ether \\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][S][C][=C][C][=C][Branch1][N][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=C][Ring1][=N][C][=C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" -6.237\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2\\n\",\n        \"output\": \" 1,2,3,4-Tetrahydronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][O]\\n\",\n        \"output\": \" Phenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" 3-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dapsone\\n\",\n        \"output\": \" Nc1ccc(cc1)S(=O)(=O)c2ccc(N)cc2\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl octanoate\\n\",\n        \"output\": \" InChI=1S/C10H20O2/c1-3-5-6-7-8-9-10(11)12-4-2/h3-9H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-4-2-3-5-7(6)8/h2-5H,8H2,1H3\\n\",\n        \"output\": \" o-Toluidine\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.00025585858869056453 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)CC(C)C\\n\",\n        \"output\": \" 5.495408738576248e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H19N5O/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" -3.239\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Cortisone\\n\",\n        \"output\": \" InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-15,18,22,26H,3-8,10-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" rainstorm\\n\",\n        \"output\": \" rainstorm does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3\\n\",\n        \"output\": \" 0.025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" m-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 5-Allyl-5-phenylbarbital\\n\",\n        \"output\": \" InChI=1S/C13H12N2O3/c1-2-8-13(9-6-4-3-5-7-9)10(16)14-12(18)15-11(13)17/h2-7H,1,8H2,(H2,14,15,16,17,18)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Chloronapthalene\\n\",\n        \"output\": \" InChI=1S/C10H7Cl/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Nonanol\\n\",\n        \"output\": \" 0.0018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Abate\\n\",\n        \"output\": \" COP(=S)(OC)Oc1ccc(Sc2ccc(OP(=S)(OC)OC)cc2)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Quinethazone\\n\",\n        \"output\": \" -3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" 0.19498445997580455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCOCCCC\\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Styrene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Ethanoyloxymethylphenytoin\\n\",\n        \"output\": \" 3.3884415613920276e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1cc(Cl)c(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" -3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Methylcyclohexane \\n\",\n        \"output\": \" 0.0001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Ethyl octanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Thiometon\\n\",\n        \"output\": \" -3.091\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H15O4P/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3\\n\",\n        \"output\": \" Triethyl phosphate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Bromoethane\\n\",\n        \"output\": \" [C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Fenthion\\n\",\n        \"output\": \" -4.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Br][Br][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" Deltamethrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][Cl]\\n\",\n        \"output\": \" 1-Chloropentane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H14O/c1-5(2)7(8)6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 3.311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Coronene\\n\",\n        \"output\": \" c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC34CCc1c(ccc2cc(O)ccc12)C3CCC4=O\\n\",\n        \"output\": \" Equilenin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Mefenacet\\n\",\n        \"output\": \" -4.873\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-2-4-6-5-3-1/h1-5H2\\n\",\n        \"output\": \" 0.933254300796991 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its oil solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H18N2O3/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Lorazepam\\n\",\n        \"output\": \" OC3N=C(c1ccccc1Cl)c2cc(Cl)ccc2NC3=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Butanone\\n\",\n        \"output\": \" CCC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Ethylhexanal\\n\",\n        \"output\": \" CCCCC(CC)C=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 3-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Triethyl phosphate\\n\",\n        \"output\": \" CCOP(=O)(OCC)OCC\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3\\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" cis 1,2-Dichloroethylene\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" NC(=O)N\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Propazine\\n\",\n        \"output\": \" CC(C)Nc1nc(Cl)nc(NC(C)C)n1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Benzamide\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Salicylamide\\n\",\n        \"output\": \" NC(=O)c1ccccc1O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Bromoacetanilide\\n\",\n        \"output\": \" InChI=1S/C8H8BrNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)CC(C)(C)O\\n\",\n        \"output\": \" 2,4-Dimethyl-2-pentanol \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Azodrin\\n\",\n        \"output\": \" 0.6509999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][C][O][Branch1][Ring1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" Fructose\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Propiconazole\\n\",\n        \"output\": \" -3.4930000000000003\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,2-Dimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Propionitrile\\n\",\n        \"output\": \" [C][C][C][#N]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1Cc2cccc3cccc1c23\\n\",\n        \"output\": \" Acenapthene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Chlorohexane\\n\",\n        \"output\": \" [C][C][C][C][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSCC\\n\",\n        \"output\": \" Phorate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][C][#C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -4.37\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility expressed as a logarithm in mol/L of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H8/c1-3-4-2/h3H,1,4H2,2H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-5-6(7)4-2/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCCCI\\n\",\n        \"output\": \" 1.5488166189124828e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15ClN2O4S/c1-8-4-3-5-9(2)14(8)18-15(20)10-6-13(23(17,21)22)11(16)7-12(10)19/h3-7,19H,1-2H3,(H,18,20)(H2,17,21,22)\\n\",\n        \"output\": \" Xipamide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H6/c1-3-4-2/h3-4H,1-2H2\\n\",\n        \"output\": \" 1,3-Butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCSSCC\\n\",\n        \"output\": \" 0.0038018939632056127 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H9N3O3/c1-5-7-4-6(9(11)12)8(5)2-3-10/h4,10H,2-3H2,1H3\\n\",\n        \"output\": \" 0.06025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Chloronapthalene\\n\",\n        \"output\": \" -3.93\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" tea\\n\",\n        \"output\": \" tea does not have SELFIES\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ncnc2nccnc12\\n\",\n        \"output\": \" 0.3419794425137088 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-4-5(2)3/h4-5H,1H2,2-3H3\\n\",\n        \"output\": \" -2.73\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Nitrobenzene\\n\",\n        \"output\": \" -1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Trichloroacetonitrile\\n\",\n        \"output\": \" ClC(Cl)(Cl)C#N\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Methyl decanoate\\n\",\n        \"output\": \" CCCCCCCCCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,3-Dimethylpyridine\\n\",\n        \"output\": \" [C][C][=C][C][=C][N][=C][Ring1][=Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Fluoroacetanilide\\n\",\n        \"output\": \" InChI=1S/C8H8FNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccccc1I\\n\",\n        \"output\": \" -3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pyrimidine\\n\",\n        \"output\": \" InChI=1S/C4H4N2/c1-2-5-4-6-3-1/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC(=O)c1ccccc1C(=O)OCC\\n\",\n        \"output\": \" Diethyl phthalate \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Hydroxyprogesterone-17a\\n\",\n        \"output\": \" CC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Methylfluorene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccccc1I\\n\",\n        \"output\": \" o-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,7-phenantroline\\n\",\n        \"output\": \" InChI=1S/C12H8N2/c1-3-9-5-6-11-10(4-2-7-13-11)12(9)14-8-1/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][Ring1][S][C][C][Branch1][C][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" Fenthion\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Difenoxuron\\n\",\n        \"output\": \" InChI=1S/C16H18N2O3/c1-18(2)16(19)17-12-4-6-14(7-5-12)21-15-10-8-13(20-3)9-11-15/h4-11H,1-3H3,(H,17,19)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Thalidomide\\n\",\n        \"output\": \" O=C1N(C2CCC(=O)NC2=O)C(=O)c3ccccc13\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccccc1NC(=O)c2c(O)cccc2\\n\",\n        \"output\": \" salicylanilide\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" ethofumesate\\n\",\n        \"output\": \" [C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Kepone\\n\",\n        \"output\": \" -5.2589999999999995\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Rovral\\n\",\n        \"output\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Oxamyl\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][N][=C][Branch1][Ring1][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-hydroxypteridine\\n\",\n        \"output\": \" [O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)C)C(C)C\\n\",\n        \"output\": \" 0.0017139573075084253 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CC=C\\n\",\n        \"output\": \" -1.614\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC1=CCC(CC1)C(C)=C\\n\",\n        \"output\": \" 5.495408738576248e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 2,6-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,3-diethylthiourea\\n\",\n        \"output\": \" [C][C][N][C][=Branch1][C][=S][N][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H\\n\",\n        \"output\": \" Anthracene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" -8.017000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4-hydroxypyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,4-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=N(=O)c1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" 1,3-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 5-Methylchrysene\\n\",\n        \"output\": \" 2.570395782768865e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" rhythm\\n\",\n        \"output\": \" rhythm does not have SELFIES\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3\\n\",\n        \"output\": \" N,N-Dimethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Fructose\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 4-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Chloropropane\\n\",\n        \"output\": \" CCCCl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC12CCC3C(CCc4cc(O)ccc34)C2CCC1=O\\n\",\n        \"output\": \" 0.00011091748152624009 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Isopentyl formate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][O][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethyl vinyl ether\\n\",\n        \"output\": \" [C][C][O][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Acrolein\\n\",\n        \"output\": \" 3.715352290971725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=O]\\n\",\n        \"output\": \" Ethyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H20O6P2S3/c1-17-23(25,18-2)21-13-5-9-15(10-6-13)27-16-11-7-14(8-12-16)22-24(26,19-3)20-4/h5-12H,1-4H3\\n\",\n        \"output\": \" Abate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H23NO3/c1-21(2)19(22(21,3)4)20(24)26-18(14-23)15-9-8-12-17(13-15)25-16-10-6-5-7-11-16/h5-13,18-19H,1-4H3\\n\",\n        \"output\": \" Fenpropathrin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][=N][O][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][C][C][C][C][Ring1][=N][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][Branch1][C][O][C][#C]\\n\",\n        \"output\": \" -5.507000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCOC\\n\",\n        \"output\": \" Methyl butyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Maltose\\n\",\n        \"output\": \" [O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1,4-Diethylbenzene \\n\",\n        \"output\": \" -3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCc1ccccc1\\n\",\n        \"output\": \" 8.709635899560814e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2,2-Dimethylbutane\\n\",\n        \"output\": \" 0.0002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Quinonamid\\n\",\n        \"output\": \" ClC(Cl)CC(=O)NC2=C(Cl)C(=O)c1ccccc1C2=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Styrene\\n\",\n        \"output\": \" InChI=1S/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][C][O][Branch1][Ring1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" 4.36515832240166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cycloheptanol\\n\",\n        \"output\": \" [O][C][C][C][C][C][C][C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H8Cl3O4P/c1-10-12(9,11-2)3(8)4(5,6)7/h3,8H,1-2H3\\n\",\n        \"output\": \" Trichlorfon\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Mirex\\n\",\n        \"output\": \" [Cl][C][Branch2][Ring1][=C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring2][Ring1][Ring1][Ring1][#C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" ethofumesate\\n\",\n        \"output\": \" InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Benzo(a)pyrene\\n\",\n        \"output\": \" 1.9998618696327446e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Formetanate\\n\",\n        \"output\": \" InChI=1S/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Chlorobiphenyl\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dinitramine\\n\",\n        \"output\": \" InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc(C)cc1\\n\",\n        \"output\": \" p-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 0.01548816618912481 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Bromo-2-methylpropane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Brc1cccc2ccccc12\\n\",\n        \"output\": \" 1-Bromonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1,8-Cineole\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,2,4,6,6'-PCB\\n\",\n        \"output\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCBr\\n\",\n        \"output\": \" 1-Bromooctane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=O]\\n\",\n        \"output\": \" Butyraldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" o-Nitrophenol\\n\",\n        \"output\": \" InChI=1S/C6H5NO3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" N,N-Diethylaniline\\n\",\n        \"output\": \" InChI=1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Carvacrol\\n\",\n        \"output\": \" c1(O)c(C)ccc(C(C)C)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=O]\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" C\\n\",\n        \"output\": \" 0.12589254117941673 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14/c1-4-6(3)5-2/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" 3-Methylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H3Br3/c7-4-1-2-5(8)6(9)3-4/h1-3H\\n\",\n        \"output\": \" 3.1622776601683795e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its oil solubility. ->\",\n        \"input\": \" CC34CCC1C(CC=C2CC(O)CCC12C)C3CCC4=O\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Oc1c(Cl)cc(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" -3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Pentyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Nitrotoluene\\n\",\n        \"output\": \" Cc1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][Cl]\\n\",\n        \"output\": \" 0.0027289777828080433 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/CCl3NO2/c2-1(3,4)5(6)7\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.07261059574351547 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 0.028183829312644536 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][=O]\\n\",\n        \"output\": \" 2-Ethylhexanal\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" FC(F)(F)c1ccccc1\\n\",\n        \"output\": \" Benzyltrifluoride\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2-Methyl-1-Pentene\\n\",\n        \"output\": \" -3.03\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" o-Chloroiodobenzene\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CH2BrCl/c2-1-3/h1H2\\n\",\n        \"output\": \" -0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 4-Chlorotoluene\\n\",\n        \"output\": \" Cc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCSCCSP(=S)(OC)OC\\n\",\n        \"output\": \" Thiometon\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCl\\n\",\n        \"output\": \" -2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3\\n\",\n        \"output\": \" Propyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Triphenylene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H7I/c1-2-3-4/h2-3H2,1H3\\n\",\n        \"output\": \" 1-Iodopropane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" -1.9469999999999998\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Bromonapthalene\\n\",\n        \"output\": \" [Br][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.011748975549395297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3,5-7,11H,1,4H2,2H3\\n\",\n        \"output\": \" 0.02754228703338166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Tetrahydropyran \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1cccc(Cl)c1Cl\\n\",\n        \"output\": \" 2,3-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Acetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H18N4O6S/c1-3-5-14(6-4-2)12-10(15(17)18)7-9(23(13,21)22)8-11(12)16(19)20/h7-8H,3-6H2,1-2H3,(H2,13,21,22)\\n\",\n        \"output\": \" oryzalin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3\\n\",\n        \"output\": \" Camphor\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0008317637711026709 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C][C]\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Octanoyloxymethylphenytoin\\n\",\n        \"output\": \" [O][=C][N][Branch1][=C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][P][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCC\\n\",\n        \"output\": \" Butane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Barban\\n\",\n        \"output\": \" [Cl][C][C][#C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-5-3-8-12-10(2)6-4-7-11(9)12/h3-8H,1-2H3\\n\",\n        \"output\": \" -4.678999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2,2,4,6,6'-PCB\\n\",\n        \"output\": \" 4.78630092322638e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 4-Bromotoluene\\n\",\n        \"output\": \" InChI=1S/C7H7Br/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cn2cc(c1ccccc1)c(=O)c(c2)c3cccc(c3)C(F)(F)F\\n\",\n        \"output\": \" 3.58921934645005e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Rovral\\n\",\n        \"output\": \" CC(C)NC(=O)N1CC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Hexadecanol\\n\",\n        \"output\": \" 1e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC=C(C(=CC)c1ccc(O)cc1)c2ccc(O)cc2\\n\",\n        \"output\": \" Dienestrol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" ClC(Cl)(Cl)Cl\\n\",\n        \"output\": \" 0.004897788193684461 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H9NO2/c1-9-8(10)11-7-5-3-2-4-6-7/h2-6H,1H3,(H,9,10)\\n\",\n        \"output\": \" 0.01573982864466219 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Thalidomide\\n\",\n        \"output\": \" 0.002108628149933289 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Bromo-2-methylpropane\\n\",\n        \"output\": \" InChI=1S/C4H9Br/c1-4(2)3-5/h4H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 3-Methylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Formothion\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" cis-1,2-Dimethylcyclohexane\\n\",\n        \"output\": \" -4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C4H8Cl3O4P/c1-10-12(9,11-2)3(8)4(5,6)7/h3,8H,1-2H3\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)OC(=O)Nc1cccc(Cl)c1\\n\",\n        \"output\": \" Chloropham\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" ClC1=C(Cl)C2(Cl)C3C4CC(C=C4)C3C1(Cl)C2(Cl)Cl\\n\",\n        \"output\": \" -6.307\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc1cccc(Cl)c1\\n\",\n        \"output\": \" 3-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Phenmedipham\\n\",\n        \"output\": \" COC(=O)Nc1cccc(OC(=O)Nc2cccc(C)c2)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC1CCCCC1\\n\",\n        \"output\": \" Methylcyclohexane \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring1][S][Ring2][Ring1][Ring2][C]\\n\",\n        \"output\": \" 0.00010023052380779004 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" NC(=O)N\\n\",\n        \"output\": \" Urea\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H8Cl3O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\\n\",\n        \"output\": \" 1.9054607179632483e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Pentachlorophenol\\n\",\n        \"output\": \" Oc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" DDD\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Isofenphos\\n\",\n        \"output\": \" InChI=1S/C15H24NO4PS/c1-6-18-21(22,16-11(2)3)20-14-10-8-7-9-13(14)15(17)19-12(4)5/h7-12H,6H2,1-5H3,(H,16,22)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H\\n\",\n        \"output\": \" 6.456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C]\\n\",\n        \"output\": \" Methane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][N]\\n\",\n        \"output\": \" 0.004477133041763623 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-2-3-4-5-6/h6H,2-5H2,1H3\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" p-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Propyl butyrate\\n\",\n        \"output\": \" [C][C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H19N5O/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" -2.478\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H8ClN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\\n\",\n        \"output\": \" 0.0013243415351946643 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCC#CCC\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" COc1ccc(cc1)C(c2ccc(OC)cc2)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" -6.89\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Benzo(b)fluoranthene\\n\",\n        \"output\": \" c1ccc2c(c1)c3cccc4c3c2cc5ccccc54\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Secobarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(C(C)CCC)CC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Br]\\n\",\n        \"output\": \" -1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" -3.18\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccccc1N(=O)=O\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 8.51138038202376e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2-Dibromoethane\\n\",\n        \"output\": \" [Br][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Butoxyethanol\\n\",\n        \"output\": \" [C][C][C][C][O][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Phosalone\\n\",\n        \"output\": \" -5.233\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CN(=O)=O\\n\",\n        \"output\": \" 1.8197008586099834 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\\n\",\n        \"output\": \" Dialifos\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H14N2O2S/c1-18(12-7-3-2-4-8-12)15(19)11-20-16-17-13-9-5-6-10-14(13)21-16/h2-10H,11H2,1H3\\n\",\n        \"output\": \" -4.873\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [I][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.818382931264455e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 2,2',3,4,5,5'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2,3,6-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" ClCC#N\\n\",\n        \"output\": \" 0.8090958991783823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Cyclohexanone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.0021978598727848252 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H5NO/c1-2-4-7-6(3-1)8-5-9-7/h1-5H\\n\",\n        \"output\": \" Benzoxazole\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2,4-Trimethylpentane\\n\",\n        \"output\": \" CC(C)CC(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benzene \\n\",\n        \"output\": \" c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)=CCC/C(C)=C\\\\CO\\n\",\n        \"output\": \" Nerol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2H4O2/c1-4-2-3/h2H,1H3\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Maltose\\n\",\n        \"output\": \" InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Iodobutane\\n\",\n        \"output\": \" [C][C][C][C][I]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Benzaldehyde\\n\",\n        \"output\": \" InChI=1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][C][C][Ring1][S][=C][Ring1][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Coronene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C#C\\n\",\n        \"output\": \" Ethyne\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,3,5-Tribromobenzene\\n\",\n        \"output\": \" [Br][C][=C][C][Branch1][C][Br][=C][C][Branch1][C][Br][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Aminocarb\\n\",\n        \"output\": \" 0.004365158322401661 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 4.265795188015926e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Iodopropane\\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Hexene\\n\",\n        \"output\": \" InChI=1S/C6H12/c1-3-5-6-4-2/h3H,1,4-6H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,3-Dichlorobenzene\\n\",\n        \"output\": \" Clc1cccc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1cccc(O)c1\\n\",\n        \"output\": \" 1,3-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" Cycluron\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-4-5-6-7(8)9-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" Methyl hexanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Hexyne \\n\",\n        \"output\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h1H,4-6H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCC=O\\n\",\n        \"output\": \" Caproaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Hydroxyacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Spironolactone\\n\",\n        \"output\": \" 6.714288529259523e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Nc1ccccc1O\\n\",\n        \"output\": \" -0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,2-Dichloroethane\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H4BrI/c7-5-1-3-6(8)4-2-5/h1-4H\\n\",\n        \"output\": \" p-Bromoiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][O][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" 0.05248074602497726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Trichloroacetonitrile\\n\",\n        \"output\": \" -2.168\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Furane\\n\",\n        \"output\": \" InChI=1S/C4H4O/c1-2-4-5-3-1/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Pentadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2\\n\",\n        \"output\": \" Bibenzyl \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dihexyl phthalate\\n\",\n        \"output\": \" [C][C][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H\\n\",\n        \"output\": \" 0.7943282347242815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-5(6)4-2/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 0.5754399373371569 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2,3,4,6-Tetrachlorophenol\\n\",\n        \"output\": \" 0.0007943282347242813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-2-3-6-4-5/h4H,2-3H2,1H3\\n\",\n        \"output\": \" Propyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Decanol\\n\",\n        \"output\": \" CCCCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Ethyl-1-hexanol\\n\",\n        \"output\": \" InChI=1S/C8H18O/c1-3-5-6-8(4-2)7-9/h8-9H,3-7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 2-Bromonapthalene\\n\",\n        \"output\": \" 3.9810717055349695e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H\\n\",\n        \"output\": \" -1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" Anthraquinone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)\\n\",\n        \"output\": \" Sulfanilamide\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pyrolan\\n\",\n        \"output\": \" CN(C)C(=O)Oc1cc(C)nn1c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" hexacosane\\n\",\n        \"output\": \" 4.634469197362884e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethion\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Butanol\\n\",\n        \"output\": \" [C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1cccc2ccccc12\\n\",\n        \"output\": \" 1-Napthol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCOC(=O)C\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][O]\\n\",\n        \"output\": \" Erythritol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.012882495516931342 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][Ring1][O][=Ring1][#Branch1]\\n\",\n        \"output\": \" 0.001584893192461114 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=N][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][N][Ring1][Branch2][C][C][O]\\n\",\n        \"output\": \" Metronidazole\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)\\n\",\n        \"output\": \" 0.009000000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Metolcarb\\n\",\n        \"output\": \" c1ccccc1(OC(=O)NC)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Heptanone\\n\",\n        \"output\": \" 0.03548133892335755 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H18O/c1-3-5-7-9(10)8-6-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" 5-Nonanone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(8)5(10)6(11)4(2)9/h1,11H\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Methylnaphthalene\\n\",\n        \"output\": \" InChI=1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][Branch2][C][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=N][=O]\\n\",\n        \"output\": \" 0.003404081897010009 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCC(C)CCO\\n\",\n        \"output\": \" 0.19498445997580455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Diisopropylsulfide\\n\",\n        \"output\": \" CC(C)SC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Barbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" Cyclopentane \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][#Branch1][C][C][Branch1][C][C][=C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Ethalfluralin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 9,10-Dimethylanthracene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Fenitrothion\\n\",\n        \"output\": \" InChI=1S/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Decene\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,6-Dichlorophenol\\n\",\n        \"output\": \" Oc1c(Cl)cccc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Ethylhexanal\\n\",\n        \"output\": \" InChI=1S/C8H16O/c1-3-5-6-8(4-2)7-9/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,4-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Xipamide\\n\",\n        \"output\": \" InChI=1S/C15H15ClN2O4S/c1-8-4-3-5-9(2)14(8)18-15(20)10-6-13(23(17,21)22)11(16)7-12(10)19/h3-7,19H,1-2H3,(H,18,20)(H2,17,21,22)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,3,5,6-Tetrachlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(8)5(10)6(11)4(2)9/h1,11H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C15H15ClN4O6S/c1-3-26-14(22)10-6-4-5-7-11(10)27(23,24)19-20(9-21)15-17-12(16)8-13(18-15)25-2/h4-9,19H,3H2,1-2H3\\n\",\n        \"output\": \" -4.5760000000000005\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chloroacetonitrile\\n\",\n        \"output\": \" InChI=1S/C2H2ClN/c3-1-2-4/h1H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" C(Cc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 2.39883291901949e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cccc2c1ccc3ccccc32\\n\",\n        \"output\": \" 1-Methylphenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Methyl-2-pentanone\\n\",\n        \"output\": \" 0.2137962089502232 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Dihexyl phthalate\\n\",\n        \"output\": \" -6.144\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,3-Dinitrobenzene\\n\",\n        \"output\": \" O=N(=O)c1cccc(c1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-7-5-9(3)10(4)6-8(7)2/h5-6H,1-4H3\\n\",\n        \"output\": \" 2.5703957827688645e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" C=CCCC=C\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Isopropylbenzene \\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][S][C][C]\\n\",\n        \"output\": \" Diethyl sulfide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H14F3N3O4/c1-4-17(7-8(2)3)12-10(18(20)21)5-9(13(14,15)16)6-11(12)19(22)23/h5-6H,2,4,7H2,1,3H3\\n\",\n        \"output\": \" Ethalfluralin\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][C][Cl]\\n\",\n        \"output\": \" 0.08709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Benzo(b)fluoranthene\\n\",\n        \"output\": \" -8.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC1CC2C(C1Cl)C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl\\n\",\n        \"output\": \" Chlordane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-5(2)6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" 2,3-Dimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(=O)Nc1cc(NS(=O)(=O)C(F)(F)F)c(C)cc1C\\n\",\n        \"output\": \" Mefluidide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc2ccc(Oc1ccc(cc1)N(=O)=O)c(Cl)c2\\n\",\n        \"output\": \" Nitrofen\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Pyridine\\n\",\n        \"output\": \" InChI=1S/C5H5N/c1-2-4-6-5-3-1/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC34CC(O)C1(F)C(CCC2=CC(=O)C=CC12C)C3CC(O)C4(O)C(=O)CO\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Malonic acid diethylester\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H15ClO4/c1-11(21)10-15(12-6-8-13(20)9-7-12)17-18(22)14-4-2-3-5-16(14)24-19(17)23/h2-9,15,22H,10H2,1H3\\n\",\n        \"output\": \" -5.8389999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Methyl-2-butanone\\n\",\n        \"output\": \" InChI=1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H6N4O8/c13-1-7(19,2(14)10-5(17)9-1)8(20)3(15)11-6(18)12-4(8)16/h19-20H,(H2,9,10,13,14,17)(H2,11,12,15,16,18)\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-4-3-5-8-7(6)2/h3-5H,1-2H3\\n\",\n        \"output\": \" 2,3-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" ICI\\n\",\n        \"output\": \" 0.004570881896148752 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.4125375446227554e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)\\n\",\n        \"output\": \" Acetamide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3\\n\",\n        \"output\": \" 3-Methyl-2-butanone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][O][C][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Ring1][P]\\n\",\n        \"output\": \" -1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCC(C)O\\n\",\n        \"output\": \" 2-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 4-hexylresorcinol\\n\",\n        \"output\": \" 0.0025703957827688645 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" chloropropylate\\n\",\n        \"output\": \" -4.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)c2cc(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" 2,2',3,4,5,5'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" BrCCBr\\n\",\n        \"output\": \" -1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" ClC1(C2(Cl)C3(Cl)C4(Cl)C5(Cl)C1(Cl)C3(Cl)Cl)C5(Cl)C(Cl)(Cl)C24Cl\\n\",\n        \"output\": \" -6.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Ethyl-2-hexanal\\n\",\n        \"output\": \" CCCC=C(CC)C=O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Pentachlorobenzene\\n\",\n        \"output\": \" -5.65\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C][C][C][=C][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2]\\n\",\n        \"output\": \" Carvone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCNc1nc(NC(C)C)nc(SC)n1\\n\",\n        \"output\": \" 0.0009120108393559096 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Norethisterone\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][O][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][Branch1][C][O][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Prasterone\\n\",\n        \"output\": \" CC34CCC1C(CC=C2CC(O)CCC12C)C3CCC4=O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCC(=O)CCC\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Estragole\\n\",\n        \"output\": \" 0.001202264434617413 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Altretamine\\n\",\n        \"output\": \" CN(C)c1nc(nc(n1)N(C)C)N(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCc1ccccc1C\\n\",\n        \"output\": \" 0.0006165950018614823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Thalidomide\\n\",\n        \"output\": \" [O][=C][N][Branch1][=N][C][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" chlordimeform\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" N(=Nc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" -4.45\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCC(C)(C)O\\n\",\n        \"output\": \" -1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Benzocaine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=C][Ring1][#C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" Benzo[ghi]perylene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" 0.31622776601683794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" norethindrone acetate\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][O][C][Branch2][Ring1][=C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][C][Ring1][O][C][C][C][Ring2][Ring1][C][Ring1][#C][C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC(=O)N\\n\",\n        \"output\": \" 7.079457843841379 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dimecron\\n\",\n        \"output\": \" CCN(CC)C(=O)C(=CCOP(=O)(OC)OC)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Nitromethane\\n\",\n        \"output\": \" CN(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4ClNO2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H\\n\",\n        \"output\": \" p-Chloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.3988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" methyl laurate\\n\",\n        \"output\": \" CCCCCCCCCCCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Tetradecanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ronnel\\n\",\n        \"output\": \" COP(=S)(OC)Oc1cc(Cl)c(Cl)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4BrF/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Acridine\\n\",\n        \"output\": \" InChI=1S/C13H9N/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-9H\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-6(2)5-7(3,4)8/h6,8H,5H2,1-4H3\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H8BrN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\\n\",\n        \"output\": \" brompyrazone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Quinonamid\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][C][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Furfural\\n\",\n        \"output\": \" InChI=1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Acrolein\\n\",\n        \"output\": \" InChI=1S/C3H4O/c1-2-3-4/h2-3H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,3-Dichloropropane\\n\",\n        \"output\": \" ClCCCCl\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Hydroxyacetanilide\\n\",\n        \"output\": \" InChI=1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" OCC1OC(C(O)C1O)n2cnc3c(O)ncnc23\\n\",\n        \"output\": \" Inosine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" -3.09\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,2-Dimethylpropanol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Dienochlor\\n\",\n        \"output\": \" 5.272298614228232e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1]\\n\",\n        \"output\": \" 5,6-Dimethylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given compound in room temperature? ->\",\n        \"input\": \" o-Methoxyphenol\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" 0.00588843655355589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][S][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 0.046773514128719815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][\\\\C][=C][/Cl]\\n\",\n        \"output\": \" cis 1,2-Dichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [Br][C][Br]\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H16N2O3/c1-3-5-6-10(4-2)7(13)11-9(15)12-8(10)14/h3-6H2,1-2H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 0.021827299118430014 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" o-Chlorobromobenzene\\n\",\n        \"output\": \" Clc1ccccc1Br\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSc1ccc(Cl)cc1\\n\",\n        \"output\": \" 1.8365383433483438e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][Branch1][C][C][S][C][C][S][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C]\\n\",\n        \"output\": \" vamidothion\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3\\n\",\n        \"output\": \" -4.26\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" -0.39\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Indole\\n\",\n        \"output\": \" [C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Hexane \\n\",\n        \"output\": \" CCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COC(=O)Nc1cccc(OC(=O)Nc2cccc(C)c2)c1\\n\",\n        \"output\": \" Phenmedipham\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" trans-2-Pentene \\n\",\n        \"output\": \" -2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H5N/c1-2-3-4/h2H2,1H3\\n\",\n        \"output\": \" Propionitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCC(C)O\\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H19N5S/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" Prometryn\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Octanone\\n\",\n        \"output\": \" CCCCCCC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Acrylonitrile\\n\",\n        \"output\": \" InChI=1S/C3H3N/c1-2-3-4/h2H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" Fluvalinate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,3-Benzenediol\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -7.25\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" o-Chloronitrobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Heptanone\\n\",\n        \"output\": \" [C][C][C][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -2.5810000000000004\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\\n\",\n        \"output\": \" Dibenzothiophene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Ethyl nonanoate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Di(2-ethylhexyl)-phthalate\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][Branch1][Ring1][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC12CCC3C(CCc4cc(O)ccc34)C2CCC1O\\n\",\n        \"output\": \" -5.03\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#C][Ring1][#Branch2]\\n\",\n        \"output\": \" -8.057\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC=C(C)C\\n\",\n        \"output\": \" 2-Methy-2-Butene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC34CCC1C(CC=C2CC(O)CCC12C)C3CCC4=O\\n\",\n        \"output\": \" Prasterone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H\\n\",\n        \"output\": \" 0.001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc(cc1)c2ccc(cc2)c3ccccc3\\n\",\n        \"output\": \" -7.11\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Octane\\n\",\n        \"output\": \" CCCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c1-6-2-4-7(5-3-6)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" -2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Benzo(k)fluoranthene\\n\",\n        \"output\": \" -8.49\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cyclohexyl-5-spirobarbituric acid\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O\\n\",\n        \"output\": \" -0.244\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Malathion\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][C][Branch1][N][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][Branch1][C][F][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C]\\n\",\n        \"output\": \" Cyfluthrin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Nonanone\\n\",\n        \"output\": \" CCCCCCCC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H5NO/c7-5-1-3-6-4-2-5/h1-4H,(H,6,7)\\n\",\n        \"output\": \" 4-hydroxypyridine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Carbetamide\\n\",\n        \"output\": \" [C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][O][C][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Ring1][P]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCC(=O)OC\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Decalin\\n\",\n        \"output\": \" C1CCC2CCCCC2C1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\\n\",\n        \"output\": \" 2.280342072000418 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 1,4-Dimethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H34/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3-16H2,1-2H3\\n\",\n        \"output\": \" Hexadecane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC1CCCCC1\\n\",\n        \"output\": \" Ethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Lenacil\\n\",\n        \"output\": \" InChI=1S/C13H18N2O2/c16-12-10-7-4-8-11(10)14-13(17)15(12)9-5-2-1-3-6-9/h9H,1-8H2,(H,14,17)\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Nonene \\n\",\n        \"output\": \" InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3-Pentanoyloxymethylphenytoin\\n\",\n        \"output\": \" InChI=1S/C21H22N2O4/c1-2-3-14-18(24)27-15-23-19(25)21(22-20(23)26,16-10-6-4-7-11-16)17-12-8-5-9-13-17/h4-13H,2-3,14-15H2,1H3,(H,22,26)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Sulfanilamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 1.757923613958693e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" NNc1ccccc1\\n\",\n        \"output\": \" Phenylhydrazine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H6N2O4/c1-5-2-3-6(8(10)11)4-7(5)9(12)13/h2-4H,1H3\\n\",\n        \"output\": \" 2,4-Dinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Tetrabromomethane\\n\",\n        \"output\": \" 0.0007244359600749898 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2,2',3,4,5,5',6-PCB\\n\",\n        \"output\": \" -8.94\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H15Br/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\",\n        \"output\": \" 1-Bromoheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/CBr4/c2-1(3,4)5\\n\",\n        \"output\": \" Tetrabromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H\\n\",\n        \"output\": \" 5.370317963702533e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pentane\\n\",\n        \"output\": \" InChI=1S/C5H12/c1-3-5-4-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCN(CC)c1nc(Cl)nc(NC(C)C)n1\\n\",\n        \"output\": \" Ipazine\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3\\n\",\n        \"output\": \" 7.961593504173184e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" Butamben\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Hexadecanol\\n\",\n        \"output\": \" InChI=1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,2,4-tribromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3Br3/c7-4-1-2-5(8)6(9)3-4/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.06165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11NO2/c1-9-11(7-8-15-9)12(14)13-10-5-3-2-4-6-10/h2-8H,1H3,(H,13,14)\\n\",\n        \"output\": \" Fenfuram\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H7Br2Cl2O4P/c1-10-13(9,11-2)12-3(5)4(6,7)8/h3H,1-2H3\\n\",\n        \"output\": \" Naled\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][C][C][=C]\\n\",\n        \"output\": \" 1,5-Hexadiene \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][I]\\n\",\n        \"output\": \" 0.005128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H13BrN2O2/c1-3-7(8,4-2)5(11)10-6(9)12/h3-4H2,1-2H3,(H3,9,10,11,12)\\n\",\n        \"output\": \" 0.0020892961308540386 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Hexadecane\\n\",\n        \"output\": \" -8.4\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Ethyl-p-aminobenzoate\\n\",\n        \"output\": \" 0.007943282347242814 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CC(C#C)N(C)C(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" 0.00012589254117941674 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Cn1cnc2n(C)c(=O)n(C)c(=O)c12\\n\",\n        \"output\": \" -0.8759999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" COP(=S)(OC)Oc1cc(Cl)c(I)cc1Cl\\n\",\n        \"output\": \" -6.62\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6Cl5NO2/c7-1-2(8)4(10)6(12(13)14)5(11)3(1)9\\n\",\n        \"output\": \" Quintozene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCC(=O)C\\n\",\n        \"output\": \" 2-Decanone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" COc1ccccc1N(=O)=O\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCC(C)CC\\n\",\n        \"output\": \" 6.9183097091893625e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.369\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H7NO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" Propanil\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Methyl-1,3-Butadiene \\n\",\n        \"output\": \" CC(=C)C=C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Hexyne\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C(C=CC=Cc2ccc1OCOc1c2)N3CCCCC3\\n\",\n        \"output\": \" 0.0003467368504525317 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C][C][C]\\n\",\n        \"output\": \" 4-Heptanone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3\\n\",\n        \"output\": \" 2-butenal\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H17ClO6/c1-8-5-9(19)6-12(23-4)17(8)16(20)13-10(21-2)7-11(22-3)14(18)15(13)24-17/h6-8H,5H2,1-4H3\\n\",\n        \"output\": \" Griseofulvin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OC(c1ccc(Cl)cc1)(c2ccc(Cl)cc2)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" Dicofol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Pentanol\\n\",\n        \"output\": \" CCC(O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Linuron\\n\",\n        \"output\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2]\\n\",\n        \"output\": \" Camphor\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cyclopentene \\n\",\n        \"output\": \" [C][C][C][=C][C][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-methyluracil\\n\",\n        \"output\": \" [C][N][C][=C][C][=Branch1][C][=O][NH1][C][Ring1][#Branch1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methyl t-butyl ether \\n\",\n        \"output\": \" COC(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Nc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" m-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Isopropyl acetate\\n\",\n        \"output\": \" 0.28183829312644537 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Aniline \\n\",\n        \"output\": \" Nc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Br]\\n\",\n        \"output\": \" 1-Bromoheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][/C][=C][\\\\C]\\n\",\n        \"output\": \" cis-2-Pentene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Griseofulvin\\n\",\n        \"output\": \" -3.2460000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H16N2O3/c1-4-6-11(7(3)5-2)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" Talbutal\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C=CC#N\\n\",\n        \"output\": \" Acrylonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Butyl acetate\\n\",\n        \"output\": \" InChI=1S/C5H10O2/c1-2-3-4-7-5-6/h5H,2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3-Methylpentane\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2H2Cl2/c1-2(3)4/h1H2\\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Pirimicarb\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=N][C][=Branch1][#Branch2][=N][C][Branch1][C][C][=C][Ring1][#Branch1][C][N][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc2ncccc2c1\\n\",\n        \"output\": \" Quinoline\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Ethofumesate\\n\",\n        \"output\": \" 0.00038018939632056124 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COc2ccc(Oc1ccc(NC(=O)N(C)C)cc1)cc2\\n\",\n        \"output\": \" Difenoxuron\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2HCl5/c3-1(4)2(5,6)7/h1H\\n\",\n        \"output\": \" 0.0025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCC(O)C=C\\n\",\n        \"output\": \" 1-Hexene-3-ol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H5Cl7/c11-4-2-1-3-5(4)9(15)7(13)6(12)8(3,14)10(9,16)17/h1-5H\\n\",\n        \"output\": \" -6.317\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" 6.918309709189363e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethylene\\n\",\n        \"output\": \" InChI=1S/C2H4/c1-2/h1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diosgenin\\n\",\n        \"output\": \" [C][C][Branch1][C][O][C][C][C][Branch1][C][C][C][C][C][C][C][Branch1][C][C][C][Branch1][C][C][C][C][O][C][C][Branch1][C][C][C][C][Ring1][#Branch1][O][C][Ring1][N][C][C][Ring1][S][C][Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2\\n\",\n        \"output\": \" 0.7079457843841379 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2\\n\",\n        \"output\": \" 5.011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][C][C][S][C][Ring1][Ring1][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O]\\n\",\n        \"output\": \" -5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,2,4-Trimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)N(=O)=O\\n\",\n        \"output\": \" 0.23988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Cholanthrene\\n\",\n        \"output\": \" InChI=1S/C20H14/c1-2-7-16-13(4-1)8-10-17-18-11-9-14-5-3-6-15(20(14)18)12-19(16)17/h1-8,10,12H,9,11H2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nitrapyrin\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCN(CC)C(=S)SCC(Cl)=C\\n\",\n        \"output\": \" -3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Chloronapthalene\\n\",\n        \"output\": \" Clc1ccc2ccccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Thiophenol \\n\",\n        \"output\": \" [S][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][C][=O][C][C][Branch1][C][C][C][Ring1][Branch2][O][C][=C][Branch1][C][Cl][C][Branch1][Ring1][O][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][O][C][Ring1][=C][=O]\\n\",\n        \"output\": \" -3.2460000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Ametryn\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C][Branch1][N][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Malathion\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 2,2-Dimethylpropanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Octanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CN(C)C(=O)Oc1cc(C)nn1c2ccccc2\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1cccc(I)c1\\n\",\n        \"output\": \" -3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" isocarbamid\\n\",\n        \"output\": \" C1N(C(=O)NCC(C)C)C(=O)NC1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 5,5-Diisopropylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOc1ccc(NC(N)=O)cc1\\n\",\n        \"output\": \" Dulcin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,4-Dichlorophenol \\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Thymol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2-Dinitrobenzene\\n\",\n        \"output\": \" O=N(=O)c1ccccc1N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Fenarimol\\n\",\n        \"output\": \" -4.38\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H8O2/c1-10-8(9)7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" Methyl benzoate \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Ethyl hexanoate\\n\",\n        \"output\": \" 0.0044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" -3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H10S/c1-3-5-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Cyclooctyl-5-spirobarbituric acid\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch2][C][C][C][C][C][C][C][Ring1][Branch2][C][=Branch1][C][=O][N][Ring1][#C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)(C)Cc1ccccc1\\n\",\n        \"output\": \" t-Pentylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Nimetazepam\\n\",\n        \"output\": \" InChI=1S/C16H13N3O3/c1-18-14-8-7-12(19(21)22)9-13(14)16(17-10-15(18)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C2H4Cl2/c3-1-2-4/h1-2H2\\n\",\n        \"output\": \" 1,2-Dichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1CCOCC1\\n\",\n        \"output\": \" Tetrahydropyran \\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Di-n-propylsulfide\\n\",\n        \"output\": \" InChI=1S/C6H14S/c1-3-5-7-6-4-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1cccc2c3c(C)cc4ccccc4c3ccc12\\n\",\n        \"output\": \" 5-Methylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Bromophos\\n\",\n        \"output\": \" COP(=S)(OC)Oc1cc(Cl)c(Br)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H10/c1-4-5(2)3/h4H,1-3H3\\n\",\n        \"output\": \" 2-Methy-2-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Diisopropylsulfide\\n\",\n        \"output\": \" -2.24\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Carbanilide\\n\",\n        \"output\": \" O=C(Nc1ccccc1)Nc2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\\n\",\n        \"output\": \" -2.89\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" trans-2-Heptene \\n\",\n        \"output\": \" [C][C][C][C][/C][=C][/C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C3H6O2/c1-3(4)5-2/h1-2H3\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(C)c(Cl)c1\\n\",\n        \"output\": \" Chlorotoluron\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3\\n\",\n        \"output\": \" 0.0002685344445658506 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H8/c1-4-5(2)3/h4H,1-2H2,3H3\\n\",\n        \"output\": \" -2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methylheptane\\n\",\n        \"output\": \" -5.08\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-5(7)6(2,3)4/h5,7H,1-4H3\\n\",\n        \"output\": \" 3,3-Dimethyl-2-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)Cc1ccccc1\\n\",\n        \"output\": \" -4.12\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 0.0021379620895022326 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-4-6(2)5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" -1.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCOP(=S)(NC(C)C)Oc1ccccc1C(=O)OC(C)C\\n\",\n        \"output\": \" -4.194\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" N-Ethylaniline\\n\",\n        \"output\": \" CCNc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccccc1O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccsc1\\n\",\n        \"output\": \" 0.046773514128719815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Trietazine\\n\",\n        \"output\": \" InChI=1S/C9H16ClN5/c1-4-11-8-12-7(10)13-9(14-8)15(5-2)6-3/h4-6H2,1-3H3,(H,11,12,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,3-Dichlorophenol\\n\",\n        \"output\": \" Oc1cccc(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Propylcyclopentane\\n\",\n        \"output\": \" 1.8197008586099827e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-5-6(7)4-2/h4,6-7H,2-3,5H2,1H3\\n\",\n        \"output\": \" -0.59\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,1,1-Trichloroethane\\n\",\n        \"output\": \" [C][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Methylfluorene\\n\",\n        \"output\": \" InChI=1S/C14H12/c1-10-5-4-8-13-12-7-3-2-6-11(12)9-14(10)13/h2-8H,9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Hydrocortisone \\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H17N5S/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Monolinuron\\n\",\n        \"output\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Pyridine\\n\",\n        \"output\": \" c1ccncc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Oc1c(I)cc(C#N)cc1I\\n\",\n        \"output\": \" 0.0002454708915685031 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Monotropitoside\\n\",\n        \"output\": \" COC(=O)c1ccccc1OC2OC(COC3OCC(O)C(O)C3O)C(O)C(O)C2O\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Anthracene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2-Methylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Nc1ccccc1O\\n\",\n        \"output\": \" o-Aminophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][O][Ring1][#Branch2]\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Menthone\\n\",\n        \"output\": \" InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\",\n        \"output\": \" -2.77\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dimethyl sulfide\\n\",\n        \"output\": \" InChI=1S/C2H6S/c1-3-2/h1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCN(CC)c1ccccc1\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H19O6PS2/c1-5-15-9(11)7-8(10(12)16-6-2)19-17(18,13-3)14-4/h8H,5-7H2,1-4H3\\n\",\n        \"output\": \" Malathion\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 4-Heptanol\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCC#N\\n\",\n        \"output\": \" 1.9054607179632472 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-6(7)5(2)3/h5-7H,4H2,1-3H3\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][N][C][=Branch1][C][=O][N][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][Ring1][=N]\\n\",\n        \"output\": \" isocarbamid\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][N][Branch1][=C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][P][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -6.523\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H6N4/c1-5-10-4-6-7(11-5)9-3-2-8-6/h2-4H,1H3\\n\",\n        \"output\": \" 2-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCBr\\n\",\n        \"output\": \" Bromoethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-Toluenesulfonamide \\n\",\n        \"output\": \" Cc1ccc(cc1)S(=O)(=O)N\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C16H12ClF4N3O4/c1-2-22(8-10-11(17)4-3-5-12(10)18)15-13(23(25)26)6-9(16(19,20)21)7-14(15)24(27)28/h3-7H,2,8H2,1H3\\n\",\n        \"output\": \" -6.78\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylanthracene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCC#C\\n\",\n        \"output\": \" 1-Octyne \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][=C][Branch1][Ring1][C][C][C][=O]\\n\",\n        \"output\": \" -2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Methyl-2-heptanol\\n\",\n        \"output\": \" CCCCCC(C)(C)O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Cl]\\n\",\n        \"output\": \" 0.033884415613920256 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-Methylaniline \\n\",\n        \"output\": \" Cc1ccc(N)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,3-Benzenediol\\n\",\n        \"output\": \" Oc1cccc(O)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C20H16/c1-13-14(2)20-17-9-4-3-7-15(17)11-12-19(20)18-10-6-5-8-16(13)18/h3-12H,1-2H3\\n\",\n        \"output\": \" -7.01\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.004265795188015926 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its oil solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Ethyl vinyl ether\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,3-Dichlorobenzene\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C2NC(=O)C1(CCCCC1)C(=O)N2\\n\",\n        \"output\": \" Cyclohexyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benzo(a)pyrene\\n\",\n        \"output\": \" InChI=1S/C20H12/c1-2-7-17-15(4-1)12-16-9-8-13-5-3-6-14-10-11-18(17)20(16)19(13)14/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Iodonapthalene\\n\",\n        \"output\": \" -4.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H4N4/c3-2-4-1-5-6-2/h1H,(H3,3,4,5,6)\\n\",\n        \"output\": \" Amitrole\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Styrene\\n\",\n        \"output\": \" C=Cc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Chlorzoxazone\\n\",\n        \"output\": \" -2.8310000000000004\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C3H6O/c1-3-2-4-3/h3H,2H2,1H3\\n\",\n        \"output\": \" -0.59\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Mecarbam\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H30O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12,16-19H,4-11H2,1-3H3\\n\",\n        \"output\": \" Progesterone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][C][Ring1][Branch1]\\n\",\n        \"output\": \" Cyclopentene \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H16O/c1-3-4-5-6-7-8(2)9/h3-7H2,1-2H3\\n\",\n        \"output\": \" 2-Octanone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Phenol\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OCC1OC(O)C(O)C(O)C1O\\n\",\n        \"output\": \" glucose\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)c1ccc(C)cc1\\n\",\n        \"output\": \" 4-Isopropyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Benzonitrile\\n\",\n        \"output\": \" -1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)N\\n\",\n        \"output\": \" 38.018939632056124 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Brc1ccc(I)cc1\\n\",\n        \"output\": \" p-Bromoiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Atovaquone(0,430mg/ml) - neutral\\n\",\n        \"output\": \" InChI=1S/C22H19ClO3/c23-16-11-9-14(10-12-16)13-5-7-15(8-6-13)19-20(24)17-3-1-2-4-18(17)21(25)22(19)26/h1-4,9-13,15,26H,5-8H2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethanethiol\\n\",\n        \"output\": \" CCS\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO\\n\",\n        \"output\": \" Corticosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C19H18N2O3/c1-14(22)12-13-17-18(23)20(15-8-4-2-5-9-15)21(19(17)24)16-10-6-3-7-11-16/h2-11,17H,12-13H2,1H3\\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.00010964781961431851 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" p-Nitrophenol\\n\",\n        \"output\": \" 0.18197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3\\n\",\n        \"output\": \" N,N-Diethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H3\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H12/c1-3-5-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" Pentane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5-Allyl-5-ethylbarbital\\n\",\n        \"output\": \" InChI=1S/C9H12N2O3/c1-3-5-9(4-2)6(12)10-8(14)11-7(9)13/h3H,1,4-5H2,2H3,(H2,10,11,12,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][N][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" Pyrazinamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1N(COC(=O)CCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 5.000345349769783e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" dibutyl sebacate\\n\",\n        \"output\": \" [C][C][C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 1,1,2,2-Tetrachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Chloro-2-methylpropane\\n\",\n        \"output\": \" ClCC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Methylheptane\\n\",\n        \"output\": \" CCCCCC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 1,2,3-Trimethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Cl\\\\C=C/Cl\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Anilofos\\n\",\n        \"output\": \" 3.698281797802666e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H22O4P2S4/c1-5-10-14(16,11-6-2)18-9-19-15(17,12-7-3)13-8-4/h5-9H2,1-4H3\\n\",\n        \"output\": \" 2.884031503126606e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][O][C][=O]\\n\",\n        \"output\": \" Propyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CN(C)C(=O)SCCCCOc1ccccc1\\n\",\n        \"output\": \" 0.00011830415557251647 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H18N2O3/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" Pentobarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Anilofos\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O]\\n\",\n        \"output\": \" Maltose\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3,5-Dichlorophenol\\n\",\n        \"output\": \" Oc1cc(Cl)cc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Isopropalin\\n\",\n        \"output\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)C(C)C)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,4-Pentadiene \\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Hexadecanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Nitramine\\n\",\n        \"output\": \" -3.5610000000000004\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Chlorbufam\\n\",\n        \"output\": \" [C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Br][C][=C][C][Branch1][C][Br][=C][C][Branch1][C][Br][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.5118864315095823e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,2-Dichlorotetrafluoroethane\\n\",\n        \"output\": \" InChI=1S/C2Cl2F4/c3-1(5,6)2(4,7)8\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" -3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Nitroethane\\n\",\n        \"output\": \" CCN(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2,3,4-Trimethylpentane\\n\",\n        \"output\": \" 1.584893192461114e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cyclopentane \\n\",\n        \"output\": \" C1CCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 2,3-Dichlorophenol\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 1-Heptene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ethyl decanoate\\n\",\n        \"output\": \" InChI=1S/C12H24O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h3-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Disulfoton\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][C][S][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][S][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C]\\n\",\n        \"output\": \" Prometryn\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H5ClO/c7-5-1-3-6(8)4-2-5/h1-4,8H\\n\",\n        \"output\": \" 4-Chlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Hexanol\\n\",\n        \"output\": \" CCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methyl benzoate \\n\",\n        \"output\": \" COC(=O)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.05248074602497726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,2',3,3'-PCB\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring1][=Branch1][Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Propionitrile\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C][C][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Ethylnaphthalene \\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(=S)SSC(=S)N(CC)CC\\n\",\n        \"output\": \" Disulfiram\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Nitrazepam\\n\",\n        \"output\": \" -3.7960000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Fenfuram\\n\",\n        \"output\": \" InChI=1S/C12H11NO2/c1-9-11(7-8-15-9)12(14)13-10-5-3-2-4-6-10/h2-8H,1H3,(H,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Glycerol\\n\",\n        \"output\": \" InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3\\n\",\n        \"output\": \" -0.624\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Aldrin\\n\",\n        \"output\": \" ClC1=C(Cl)C2(Cl)C3C4CC(C=C4)C3C1(Cl)C2(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C18H14/c1-3-7-15(8-4-1)17-11-13-18(14-12-17)16-9-5-2-6-10-16/h1-14H\\n\",\n        \"output\": \" -7.11\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(=C)C1CC=C(C)C(=O)C1\\n\",\n        \"output\": \" Carvone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C3H6Cl2/c4-2-1-3-5/h1-3H2\\n\",\n        \"output\": \" 1,3-Dichloropropane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methylphenanthrene\\n\",\n        \"output\": \" InChI=1S/C15H12/c1-11-6-9-15-13(10-11)8-7-12-4-2-3-5-14(12)15/h2-10H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC1CCCO1\\n\",\n        \"output\": \" 1.288249551693134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2\\n\",\n        \"output\": \" 1e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl\\n\",\n        \"output\": \" Endrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" OC1CCCCCCC1\\n\",\n        \"output\": \" Cyclooctanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C17H17ClO6/c1-8-5-9(19)6-12(23-4)17(8)16(20)13-10(21-2)7-11(22-3)14(18)15(13)24-17/h6-8H,5H2,1-4H3\\n\",\n        \"output\": \" 0.0005675446054085465 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H14O/c1-3-5-7(8)6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" 4-Heptanone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Trichloroethylene\\n\",\n        \"output\": \" ClC=C(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Diphenylmethane\\n\",\n        \"output\": \" C(c1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Nitroanisole\\n\",\n        \"output\": \" InChI=1S/C7H7NO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H3Cl4N/c7-5-3-1-2-4(11-5)6(8,9)10/h1-3H\\n\",\n        \"output\": \" -3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C17H12Cl2N2O/c18-14-7-5-12(6-8-14)17(22,13-9-20-11-21-10-13)15-3-1-2-4-16(15)19/h1-11,22H\\n\",\n        \"output\": \" -4.38\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Pyrimidine\\n\",\n        \"output\": \" 12.589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C]\\n\",\n        \"output\": \" Ethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C11H21N5OS/c1-8(2)13-10-14-9(12-6-5-7-17-3)15-11(16-10)18-4/h8H,5-7H2,1-4H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" -2.928\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.2589254117941662e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)C(=O)C\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C25H28O3/c1-4-27-22-15-13-21(14-16-22)25(2,3)19-26-18-20-9-8-12-24(17-20)28-23-10-6-5-7-11-23/h5-17H,4,18-19H2,1-3H3\\n\",\n        \"output\": \" Etofenprox\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H19N5S/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" Terbutryn\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Dioxacarb\\n\",\n        \"output\": \" -1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O]\\n\",\n        \"output\": \" Ethanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" rhodanine\\n\",\n        \"output\": \" [C][S][C][=Branch1][C][=S][N][C][Ring1][=Branch1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [I][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Iodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1cccc(Cl)c1Cl\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Bromonapthalene\\n\",\n        \"output\": \" Brc1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" meconin\\n\",\n        \"output\": \" -1.899\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Napthol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -4.376\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H8N2/c7-8-6-4-2-1-3-5-6/h1-5,8H,7H2\\n\",\n        \"output\": \" Phenylhydrazine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][Branch1][O][C][O][C][=Branch1][C][=O][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Pentanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Carbofuran\\n\",\n        \"output\": \" 0.001584893192461114 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Propetamphos\\n\",\n        \"output\": \" -3.408\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H6N2O2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H,7H2\\n\",\n        \"output\": \" 0.006456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Prometon\\n\",\n        \"output\": \" InChI=1S/C10H19N5O/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(c(Cl)c1)n2nc(oc2=O)C(C)(C)C\\n\",\n        \"output\": \" Dimefuron\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10Cl10/c11-1-2(12)6(16)9(19,5(1)15)10(20)7(17)3(13)4(14)8(10)18\\n\",\n        \"output\": \" Dienochlor\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 0.0007585775750291836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H13F3N2O3S/c1-6-4-7(2)10(5-9(6)15-8(3)17)16-20(18,19)11(12,13)14/h4-5,16H,1-3H3,(H,15,17)\\n\",\n        \"output\": \" Mefluidide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][Branch1][=Branch2][C][O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Propanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propetamphos\\n\",\n        \"output\": \" CCNP(=S)(OC)OC(=CC(=O)OC(C)C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benzyltrifluoride\\n\",\n        \"output\": \" InChI=1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Atovaquone(0,430mg/ml) - neutral\\n\",\n        \"output\": \" 1.1721953655481303e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Epitostanol\\n\",\n        \"output\": \" 3.890451449942805e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Propylene\\n\",\n        \"output\": \" [C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Nitroaniline\\n\",\n        \"output\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC(=O)C(C)(C)C\\n\",\n        \"output\": \" -0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Fluometuron\\n\",\n        \"output\": \" 0.0003715352290971724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H12F3NO4S2/c1-10-9-12(23(19,20)11-5-3-2-4-6-11)7-8-13(10)18-24(21,22)14(15,16)17/h2-9,18H,1H3\\n\",\n        \"output\": \" 0.00015848931924611142 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][S][P][=Branch1][C][=O][Branch1][=Branch1][S][C][C][C][C][S][C][C][C][C]\\n\",\n        \"output\": \" 7.244359600749906e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Methyl-3-heptanol\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1ccc(Cl)cc1\\n\",\n        \"output\": \" 1,4-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Iodoheptane\\n\",\n        \"output\": \" InChI=1S/C7H15I/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Phenol\\n\",\n        \"output\": \" c1ccccc1O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Ethyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,3-Butadiene\\n\",\n        \"output\": \" [C][=C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.03311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 1,2,4,5-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3\\n\",\n        \"output\": \" 8.91250938133746e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCC(=O)CCCC\\n\",\n        \"output\": \" 5-Nonanone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Butene\\n\",\n        \"output\": \" [C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethyl nonanoate\\n\",\n        \"output\": \" CCCCCCCCC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Nitronapthalene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Thymol\\n\",\n        \"output\": \" CC(C)c1ccc(C)cc1O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-6-15-12-19-17-10-4-8-13-7-3-9-16(20(13)17)18(19)11-14(15)5-1/h1-12H\\n\",\n        \"output\": \" Benzo(k)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" -1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CON(C)C(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" 0.0026915348039269166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][C][O][Ring1][Branch1]\\n\",\n        \"output\": \" Dioxacarb\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" c1(C#N)c(Cl)c(C#N)c(Cl)c(Cl)c(Cl)1\\n\",\n        \"output\": \" -5.64\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" Tetradecane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1,4-Cyclohexadiene\\n\",\n        \"output\": \" -2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,2',3,3'-PCB\\n\",\n        \"output\": \" InChI=1S/C12H6Cl4/c13-9-5-1-3-7(11(9)15)8-4-2-6-10(14)12(8)16/h1-6H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 4-Methylbiphenyl\\n\",\n        \"output\": \" -4.62\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][N][C]\\n\",\n        \"output\": \" Metolcarb\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" isocarbamid\\n\",\n        \"output\": \" -2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][O][=O]\\n\",\n        \"output\": \" 1.4487718535447632e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)S(N)(=O)=O)N(=O)=O\\n\",\n        \"output\": \" -5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Cyclobutyl-5-spirobarbituric acid\\n\",\n        \"output\": \" -1.655\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCCCCCCCCCCCO\\n\",\n        \"output\": \" -6.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1cc(Cl)cc(Cl)c1Cl\\n\",\n        \"output\": \" 0.0021379620895022326 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" FC(F)(F)c1cccc(c1)N2CC(CCl)C(Cl)C2=O\\n\",\n        \"output\": \" 8.974287945007491e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C]\\n\",\n        \"output\": \" -1.614\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3,4-Dichloronitrobenzene\\n\",\n        \"output\": \" -3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Pentyl propanoate\\n\",\n        \"output\": \" CCCCC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C17H12/c1-2-6-13-11-17-15(9-12(13)5-1)10-14-7-3-4-8-16(14)17/h1-9,11H,10H2\\n\",\n        \"output\": \" -8.04\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Parathion\\n\",\n        \"output\": \" 2.187761623949552e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzo(a)pyrene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Acetamide\\n\",\n        \"output\": \" CC(=O)N\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1ccc(Cl)cc1C(c2ccc(Cl)cc2)(O)C(=O)OC(C)C\\n\",\n        \"output\": \" chloropropylate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-methylpteridine\\n\",\n        \"output\": \" [C][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][S][C][C][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C]\\n\",\n        \"output\": \" Thiometon\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][=C]\\n\",\n        \"output\": \" 5.495408738576248e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Chlorazine\\n\",\n        \"output\": \" 3.881503659906478e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2',3,4,4',5',6-PCB\\n\",\n        \"output\": \" Clc1ccc(c(Cl)c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12/c1-3-5-6-4-2/h3H,1,4-6H2,2H3\\n\",\n        \"output\": \" 1-Hexene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -5.696000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Mecarbam\\n\",\n        \"output\": \" CCOC(=O)N(C)C(=O)CSP(=S)(OCC)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4-Bromotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pentachloroethane\\n\",\n        \"output\": \" InChI=1S/C2HCl5/c3-1(4)2(5,6)7/h1H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 5,5-Diisopropylbarbital\\n\",\n        \"output\": \" -2.766\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch2][C][C][C][C][C][C][C][Ring1][Branch2][C][=Branch1][C][=O][N][Ring1][#C]\\n\",\n        \"output\": \" -2.9819999999999998\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Bromopentane\\n\",\n        \"output\": \" -3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Terbumeton\\n\",\n        \"output\": \" InChI=1S/C10H19N5O/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][Branch1][Branch2][N][=C][N][Branch1][C][C][C][=C][Ring1][O]\\n\",\n        \"output\": \" Formetanate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethyl hexanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][=C]\\n\",\n        \"output\": \" 1-Hexene-3-ol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethyl octanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H14N2O/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19/h3-10H,1-2H3\\n\",\n        \"output\": \" -2.925\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Phenetole\\n\",\n        \"output\": \" [C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1(C(C)(C)C)cc(C(C)(C)C)cc(OC(=O)NC)c1\\n\",\n        \"output\": \" -4.24\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4Br2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\",\n        \"output\": \" -4.07\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=O]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Diethyl phthalate \\n\",\n        \"output\": \" InChI=1S/C12H14O4/c1-3-15-11(13)9-7-5-6-8-10(9)12(14)16-4-2/h5-8H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methyl butyl ether \\n\",\n        \"output\": \" [C][C][C][C][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1-Hexanol\\n\",\n        \"output\": \" -1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Coumaphos\\n\",\n        \"output\": \" 4.149540426343624e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Ethyltoluene\\n\",\n        \"output\": \" CCc1ccccc1C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-4-5(2)3/h4H,1-3H3\\n\",\n        \"output\": \" 0.002754228703338166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCC=C\\n\",\n        \"output\": \" 1-Decene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][O][C][C]\\n\",\n        \"output\": \" 0.21877616239495523 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccc2c(ccc3ccccc32)c1\\n\",\n        \"output\": \" 1.445439770745928e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H16N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h5H,4,6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" 5-(3-Methyl-2-butenyl)-5-ethylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Maltose\\n\",\n        \"output\": \" 2.280342072000418 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3,4-Dimethylpyridine\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Isobutyl formate\\n\",\n        \"output\": \" CC(C)COC=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-Bromophenol\\n\",\n        \"output\": \" Oc1ccc(Br)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14/c1-4-5-6(2)3/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.00018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-5(2)4-6(3)7/h5-7H,4H2,1-3H3\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1c(Cl)c(Cl)c(N(=O)=O)c(Cl)c1Cl\\n\",\n        \"output\": \" -5.82\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cycloheptane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][C][#C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Barban\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Phenol\\n\",\n        \"output\": \" InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H7ClO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3\\n\",\n        \"output\": \" -2.78\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCOC(C)C\\n\",\n        \"output\": \" Propylisopropylether\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][O][C][C][C][C]\\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5-Ethyl-5-phenylbarbital\\n\",\n        \"output\": \" InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benfluralin\\n\",\n        \"output\": \" InChI=1S/C13H16F3N3O4/c1-3-5-6-17(4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Anethole\\n\",\n        \"output\": \" 0.0007413102413009177 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCCCc1ccccc1\\n\",\n        \"output\": \" -5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" temple\\n\",\n        \"output\": \" temple does not have compound\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" 2,2',3,4,5,5',6-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.148\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\\n\",\n        \"output\": \" -5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3\\n\",\n        \"output\": \" Butyraldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1c(OC)c(OC)C2C(=O)OCC2c1\\n\",\n        \"output\": \" -1.899\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Chlortoluron\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,6-Dichlorophenol\\n\",\n        \"output\": \" 0.0162181009735893 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc2c(c1)sc3ccccc23\\n\",\n        \"output\": \" 4.168693834703355e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" m-Chloronitrobenzene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Aniline \\n\",\n        \"output\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Butyne\\n\",\n        \"output\": \" InChI=1S/C4H6/c1-3-4-2/h1H,4H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H8FNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\",\n        \"output\": \" p-Fluoroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methylheptane\\n\",\n        \"output\": \" InChI=1S/C8H18/c1-4-5-6-7-8(2)3/h8H,4-7H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)c2ccccc2\\n\",\n        \"output\": \" 4-Methylbiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H13ClN2O/c1-4-9(2)15(3)12(16)14-11-7-5-10(13)6-8-11/h1,5-9H,2-3H3,(H,14,16)\\n\",\n        \"output\": \" 0.00012589254117941674 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Mebendazole\\n\",\n        \"output\": \" InChI=1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Di(2-ethylhexyl)-phthalate\\n\",\n        \"output\": \" InChI=1S/C24H38O4/c1-5-9-13-19(7-3)17-27-23(25)21-15-11-12-16-22(21)24(26)28-18-20(8-4)14-10-6-2/h11-12,15-16,19-20H,5-10,13-14,17-18H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Diethyl ether \\n\",\n        \"output\": \" CCOCC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" BrC(Br)(Br)Br\\n\",\n        \"output\": \" Tetrabromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" rhodanine\\n\",\n        \"output\": \" -1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Clc1ccccc1Cl\\n\",\n        \"output\": \" 0.0008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Siduron\\n\",\n        \"output\": \" InChI=1S/C14H20N2O/c1-11-7-5-6-10-13(11)16-14(17)15-12-8-3-2-4-9-12/h2-4,8-9,11,13H,5-7,10H2,1H3,(H2,15,16,17)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Amobarbital\\n\",\n        \"output\": \" CCC1(CCC(C)C)C(=O)NC(=O)NC1=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" DDT\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H17O2PS3/c1-4-8-10(11,9-5-2)13-7-12-6-3/h4-7H2,1-3H3\\n\",\n        \"output\": \" -4.11\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 1-Octene \\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Butyraldehyde\\n\",\n        \"output\": \" [C][C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,2,4,5-Tetrabromobenzene\\n\",\n        \"output\": \" -6.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=Branch1][C][=S][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Phenylthiourea\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1,2,4-Trimethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.17\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC(C)Oc1cc(c(Cl)cc1Cl)n2nc(oc2=O)C(C)(C)C\\n\",\n        \"output\": \" -5.696000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Propanol\\n\",\n        \"output\": \" InChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Triazolam\\n\",\n        \"output\": \" InChI=1S/C17H12Cl2N4/c1-10-21-22-16-9-20-17(12-4-2-3-5-14(12)19)13-8-11(18)6-7-15(13)23(10)16/h2-8H,9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Hexadecane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Heptyne\\n\",\n        \"output\": \" InChI=1S/C7H12/c1-3-5-7-6-4-2/h1H,4-7H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Dichloromethane\\n\",\n        \"output\": \" 0.2344228815319922 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][N][Cl]\\n\",\n        \"output\": \" -5.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Cc2c(N)c(=O)n(c1ccccc1)n2C\\n\",\n        \"output\": \" -0.624\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Chloropentane\\n\",\n        \"output\": \" CCCCCCl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)N(=O)=O\\n\",\n        \"output\": \" 2-Nitropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Disulfiram\\n\",\n        \"output\": \" InChI=1S/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][N][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=Branch1][N][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" -3.408\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccc(C)c(C)c1\\n\",\n        \"output\": \" 0.0004897788193684461 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c1-6-2-4-7(5-3-6)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" p-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(=O)CCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylnapthalene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/CH4/h1H4\\n\",\n        \"output\": \" 0.12589254117941673 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCC=O\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCNC(=S)NCC\\n\",\n        \"output\": \" 1,3-diethylthiourea\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Isofenphos\\n\",\n        \"output\": \" CCOP(=S)(NC(C)C)Oc1ccccc1C(=O)OC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,4-Dimethyl-2-pentanol \\n\",\n        \"output\": \" CC(C)CC(C)(C)O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=Branch1][=C][=C][Branch1][C][Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl][Cl]\\n\",\n        \"output\": \" -4.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its oil solubility expressed as a logarithm in mol/L. ->\",\n        \"input\": \" CCCCCBr\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Formothion\\n\",\n        \"output\": \" InChI=1S/C6H12NO4PS2/c1-7(5-8)6(9)4-14-12(13,10-2)11-3/h5H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H9NO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Pentyne\\n\",\n        \"output\": \" CCCC#C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCCCCC(=O)OCC\\n\",\n        \"output\": \" -3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Norea\\n\",\n        \"output\": \" CN(C)C(=O)NC1CC2CC1C3CCCC23\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H13ClN2O2/c1-5-6(10)7(13)12(8(14)11-5)9(2,3)4/h1-4H3,(H,11,14)\\n\",\n        \"output\": \" Terbacil\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" rhodanine\\n\",\n        \"output\": \" C1SC(=S)NC1(=O)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][Ring1][O][=Ring1][#Branch1]\\n\",\n        \"output\": \" Carbofuran\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Sulfanilamide\\n\",\n        \"output\": \" InChI=1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H5NO/c7-5-1-3-6-4-2-5/h1-4H,(H,6,7)\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ametryn\\n\",\n        \"output\": \" [C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC(=C(Cl)C(=C(Cl)Cl)Cl)Cl\\n\",\n        \"output\": \" Hexachloro-1,3-butadiene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dulcin\\n\",\n        \"output\": \" CCOc1ccc(NC(N)=O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COc1cccc(Cl)c1\\n\",\n        \"output\": \" 0.0016595869074375613 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" o-Chloronitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylbutanol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC\\n\",\n        \"output\": \" Ethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Fluoromethalone\\n\",\n        \"output\": \" -4.099\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C][C][C]\\n\",\n        \"output\": \" Ethyl pentanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Benzenediol\\n\",\n        \"output\": \" Oc1ccc(O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,4-Dichlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Iodobenzene\\n\",\n        \"output\": \" [I][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Linuron\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 7-methoxypteridine\\n\",\n        \"output\": \" COc2cnc1cncnc1n2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" p-Chlorobromobenzene\\n\",\n        \"output\": \" 0.00023442288153199226 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc(C)c2ccccc12\\n\",\n        \"output\": \" 1,4-Dimethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(=C)C\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Methoproptryne\\n\",\n        \"output\": \" InChI=1S/C11H21N5OS/c1-8(2)13-10-14-9(12-6-5-7-17-3)15-11(16-10)18-4/h8H,5-7H2,1-4H3,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Oc1ccc(Cl)cc1Cc2cc(Cl)ccc2O\\n\",\n        \"output\": \" 0.00011142945335917292 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Isobutyl formate\\n\",\n        \"output\": \" InChI=1S/C5H10O2/c1-5(2)3-7-4-6/h4-5H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C13H8Cl2N2O4/c14-7-1-4-12(18)9(5-7)13(19)16-11-3-2-8(17(20)21)6-10(11)15/h1-6,18H,(H,16,19)\\n\",\n        \"output\": \" 1.9952623149688786e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC=C\\n\",\n        \"output\": \" 1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccccc1\\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H13N3O3/c1-18-14-8-7-12(19(21)22)9-13(14)16(17-10-15(18)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\\n\",\n        \"output\": \" Nimetazepam\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2-Octanone\\n\",\n        \"output\": \" -2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.004786300923226385 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][N][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Pyrimidine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-4-2-3-5-7(6)8/h2-5H,8H2,1H3\\n\",\n        \"output\": \" 0.006165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC12CCC(CC1)C(C)(C)O2\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" m-Chloroaniline\\n\",\n        \"output\": \" 0.04265795188015926 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methyl hexanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Carboxin\\n\",\n        \"output\": \" CC1=C(SCCO1)C(=O)Nc2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCCCO\\n\",\n        \"output\": \" 0.01548816618912481 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H\\n\",\n        \"output\": \" benzoin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methyl decanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Niclosamide\\n\",\n        \"output\": \" InChI=1S/C13H8Cl2N2O4/c14-7-1-4-12(18)9(5-7)13(19)16-11-3-2-8(17(20)21)6-10(11)15/h1-6,18H,(H,16,19)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Isopropylbenzene \\n\",\n        \"output\": \" CC(C)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCOC(=O)CCCCCCCCC(=O)OCCCC\\n\",\n        \"output\": \" dibutyl sebacate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Cyclohexene\\n\",\n        \"output\": \" C1CCC=CC1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Fluoranthene\\n\",\n        \"output\": \" -6.0\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Fluorometuron\\n\",\n        \"output\": \" InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H12N2O3/c1-3-5-9(4-2)6(12)10-8(14)11-7(9)13/h3H,1,4-5H2,2H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" 0.024322040090738146 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H10/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" Biphenyl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2\\n\",\n        \"output\": \" 4-Pentene-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)\\n\",\n        \"output\": \" Isonazid\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C15H18Cl2N2O3/c1-8(2)21-12-7-11(9(16)6-10(12)17)19-14(20)22-13(18-19)15(3,4)5/h6-8H,1-5H3\\n\",\n        \"output\": \" 2.0137242498623855e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][O][C][Branch2][Ring2][O][C][Branch1][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][=Branch1][Ring2][Ring1][C][C][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" -4.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Ethanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H25NO2/c1-15(2,3)11-8-12(16(4,5)6)10-13(9-11)19-14(18)17-7/h8-10H,1-7H3,(H,17,18)\\n\",\n        \"output\": \" 5.7543993733715664e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][Cl]\\n\",\n        \"output\": \" 0.0018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" benzoin\\n\",\n        \"output\": \" [O][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][Ring1][C][C][C][=O]\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Napthylamine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cn1c(=O)n(C)c2nc[nH]c2c1=O\\n\",\n        \"output\": \" Theophylline\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H10ClNO2/c1-3-8(2)15-11(14)13-10-6-4-5-9(12)7-10/h1,4-8H,2H3,(H,13,14)\\n\",\n        \"output\": \" Chlorbufam\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Isopropyl formate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][O][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-Chlorophenol \\n\",\n        \"output\": \" Oc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC\\n\",\n        \"output\": \" Propane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H6N4O8/c13-1-7(19,2(14)10-5(17)9-1)8(20)3(15)11-6(18)12-4(8)16/h19-20H,(H2,9,10,13,14,17)(H2,11,12,15,16,18)\\n\",\n        \"output\": \" alloxantin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-7-5-4-6-8(2)9(7)3/h4-6H,1-3H3\\n\",\n        \"output\": \" -3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility of given compound. ->\",\n        \"input\": \" p-Methylaniline \\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H15NO2/c1-2-3-8-14-11(13)9-4-6-10(12)7-5-9/h4-7H,2-3,8,12H2,1H3\\n\",\n        \"output\": \" 0.0008279421637123345 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(Br)(CC)C(=O)NC(N)=O\\n\",\n        \"output\": \" Carbromal\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethyl decanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Chloropentane\\n\",\n        \"output\": \" -2.73\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12NO4PS2/c1-7(5-8)6(9)4-14-12(13,10-2)11-3/h5H,4H2,1-3H3\\n\",\n        \"output\": \" -1.995\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H11Br/c1-2-3-4-5-6/h2-5H2,1H3\\n\",\n        \"output\": \" -3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][O][C][=O]\\n\",\n        \"output\": \" -1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 1,2-Dichlorotetrafluoroethane\\n\",\n        \"output\": \" 0.0018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)c1ccc(NC(=O)N(C)C)cc1\\n\",\n        \"output\": \" Isoproturon\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12/c1-4-5-6(2)3/h2,4-5H2,1,3H3\\n\",\n        \"output\": \" 2-Methyl-1-Pentene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methylpropan-1-ol\\n\",\n        \"output\": \" 1.2589254117941673 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Picene\\n\",\n        \"output\": \" 1.3489628825916533e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2,3,4-Tetrachlorobenzene\\n\",\n        \"output\": \" Clc1ccc(Cl)c(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Branch1][C][F][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][Ring1][Branch1][C][C][C][Ring2][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" -5.6129999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" Bromophos\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" m-Nitrophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-5(2)3-7-4-6/h4-5H,3H2,1-2H3\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8Cl4N2/c9-5-3(1-13)6(10)8(12)7(11)4(5)2-14\\n\",\n        \"output\": \" -5.64\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Spironolactone\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][S][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][C][C][C][Branch1][C][C][C][Branch1][#C][C][C][C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][O][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][Ring1][#C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCC(O)CC\\n\",\n        \"output\": \" -1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propylisopropylether\\n\",\n        \"output\": \" CCCOC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" d-inositol\\n\",\n        \"output\": \" 2.2387211385683394 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CO\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Fenfuram\\n\",\n        \"output\": \" 0.0005011872336272725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Antipyrene\\n\",\n        \"output\": \" 5.188000389289611 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Mirex\\n\",\n        \"output\": \" InChI=1S/C10Cl12/c11-1-2(12)7(17)4(14)3(13,5(1,15)9(7,19)20)6(1,16)10(21,22)8(2,4)18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(CC)C=O\\n\",\n        \"output\": \" 2-Ethylbutanal\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\\n\",\n        \"output\": \" ethofumesate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" Cypermethrin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\\n\",\n        \"output\": \" 0.0003467368504525317 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)CCC(C)(C)C\\n\",\n        \"output\": \" 2,2,5-Trimethylhexane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCCCCc1ccccc1\\n\",\n        \"output\": \" 2.290867652767775e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" 0.003981071705534973 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" o-Nitroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Br]\\n\",\n        \"output\": \" -1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Bromobutane\\n\",\n        \"output\": \" -2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 3,3-Dimethyl-2-butanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Diiodomethane\\n\",\n        \"output\": \" ICI\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][O][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" Ethyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Methyl-2-heptanol\\n\",\n        \"output\": \" 0.019054607179632473 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Ethyl-3-pentanol\\n\",\n        \"output\": \" CCC(O)(CC)CC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc2ccc1oc(=O)c(Cl)c(C)c1c2\\n\",\n        \"output\": \" -5.382000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,4-Cyclohexadiene\\n\",\n        \"output\": \" InChI=1S/C6H8/c1-2-4-6-5-3-1/h1-2,5-6H,3-4H2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][Branch1][C][C][C][C][C][C][C][=C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][C][C][C][Ring2][Ring1][Branch1][Ring1][P][C]\\n\",\n        \"output\": \" Medrogestone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Neburon\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Hexadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4-Methylbiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methyl propyl ether \\n\",\n        \"output\": \" InChI=1S/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 2-Methylpentanol\\n\",\n        \"output\": \" 0.07762471166286916 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3\\n\",\n        \"output\": \" Fluoromethalone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethyl-p-hydroxybenzoate \\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2-pyrrolidone\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Oc1cccc(Cl)c1\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccccc1C2=NCC(=O)Nc3ccc(cc23)N(=O)=O\\n\",\n        \"output\": \" Clonazepam\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Ethyl pyridine\\n\",\n        \"output\": \" CCc1ccccn1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][C][Ring1][=C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" -8.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C=C\\n\",\n        \"output\": \" 3-Methyl-1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Cholanthrene\\n\",\n        \"output\": \" [C][C][C][=C][C][Ring1][Branch1][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H10N2O4/c16-10-6-5-9(11(17)14-10)15-12(18)7-3-1-2-4-8(7)13(15)19/h1-4,9H,5-6H2,(H,14,16,17)\\n\",\n        \"output\": \" 0.002108628149933289 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cyclooctanol\\n\",\n        \"output\": \" [O][C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\\n\",\n        \"output\": \" Fluometuron\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Nitrophenol\\n\",\n        \"output\": \" InChI=1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-5-7-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" -1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benzyltrifluoride\\n\",\n        \"output\": \" FC(F)(F)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Tetradecanol\\n\",\n        \"output\": \" -5.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCNc1nc(NC(C)C)nc(OC)n1\\n\",\n        \"output\": \" Atratone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3-Propanoyloxymethylphenytoin\\n\",\n        \"output\": \" [O][=C][N][Branch1][=Branch2][C][O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Fenthion\\n\",\n        \"output\": \" InChI=1S/C10H15O3PS2/c1-8-7-9(5-6-10(8)16-4)13-14(15,11-2)12-3/h5-7H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H\\n\",\n        \"output\": \" -3.5039999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][S][C]\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccncc1\\n\",\n        \"output\": \" Pyridine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1,2,3,4-Tetrahydronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" NNc1ccccc1\\n\",\n        \"output\": \" 1.1748975549395295 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" diisooctyl phthalate\\n\",\n        \"output\": \" c1(C(=O)OCCCCCC(C)(C))c(C(=O)OCCCCCC(C)(C))cccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-ethylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Bromopropane\\n\",\n        \"output\": \" InChI=1S/C3H7Br/c1-3(2)4/h3H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C4H8Cl3O4P/c1-10-12(9,11-2)3(8)4(5,6)7/h3,8H,1-2H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C15H17Cl2N3O2/c1-2-3-12-7-21-15(22-12,8-20-10-18-9-19-20)13-5-4-11(16)6-14(13)17/h4-6,9-10,12H,2-3,7-8H2,1H3\\n\",\n        \"output\": \" 0.00032136605386403147 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][=N]\\n\",\n        \"output\": \" Cyclohexyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Dodecanol\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Nimetazepam\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H\\n\",\n        \"output\": \" 2-Chlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][=N][O][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][C][C][C][C][Ring1][=N][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][Branch1][C][O][C][#C]\\n\",\n        \"output\": \" Danazol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Methylbutan-1-ol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Decene\\n\",\n        \"output\": \" InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methazole\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][N][Branch1][#C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring1][=C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H25NO2/c1-15(2,3)11-8-12(16(4,5)6)10-13(9-11)19-14(18)17-7/h8-10H,1-7H3,(H,17,18)\\n\",\n        \"output\": \" butacarb\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" o-Nitrotoluene\\n\",\n        \"output\": \" InChI=1S/C7H7NO2/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H5Cl5/c13-6-4-9(16)12(10(17)5-6)11-7(14)2-1-3-8(11)15/h1-5H\\n\",\n        \"output\": \" 4.78630092322638e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Diethylbenzene \\n\",\n        \"output\": \" CCc1ccc(CC)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][=C][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][Cl][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Flumetralin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Glafenine\\n\",\n        \"output\": \" OCC(O)COC(=O)c1ccccc1Nc2ccnc3cc(Cl)ccc23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" OCC1OC(O)C(O)C(O)C1O\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N]\\n\",\n        \"output\": \" Methoproptryne\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chloramphenicol\\n\",\n        \"output\": \" OCC(NC(=O)C(Cl)Cl)C(O)c1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Cyclobutyl-5-spirobarbituric acid\\n\",\n        \"output\": \" O=C2NC(=O)C1(CCC1)C(=O)N2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,6-Dimethylphenol\\n\",\n        \"output\": \" InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H9Cl5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H\\n\",\n        \"output\": \" -5.666\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Nonanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CN2C(=O)CN=C(c1ccccc1)c3cc(ccc23)N(=O)=O\\n\",\n        \"output\": \" 0.0001599558028614668 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Methylphenol\\n\",\n        \"output\": \" InChI=1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" NC(=O)c1ccccc1O\\n\",\n        \"output\": \" Salicylamide\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2-Dibromoethane\\n\",\n        \"output\": \" InChI=1S/C2H4Br2/c3-1-2-4/h1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-3-9-5-7-10(4-2)8-6-9/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" 1,4-Diethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Cyfluthrin\\n\",\n        \"output\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2ccc(F)c(Oc3ccccc3)c2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Fenothiocarb\\n\",\n        \"output\": \" -3.927\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)CCC(C)(C)C\\n\",\n        \"output\": \" 8.91250938133746e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H\\n\",\n        \"output\": \" Diphenylamine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CN(C)C(=O)Nc2ccc(Oc1ccc(Cl)cc1)cc2\\n\",\n        \"output\": \" 1.2882495516931348e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -6.29\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][=C]\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [I][C][I]\\n\",\n        \"output\": \" -2.34\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,5-Dimethlnapthalene\\n\",\n        \"output\": \" InChI=1S/C12H12/c1-9-5-3-8-12-10(2)6-4-7-11(9)12/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" OCC(NC(=O)C(Cl)Cl)C(O)c1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 0.007744617978025192 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=N][C][=C][C][Branch1][#Branch1][C][=Branch1][C][=O][N][N][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.009000000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Clomazone\\n\",\n        \"output\": \" CC1(C)CON(Cc2ccccc2Cl)C1=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-Fluoroacetanilide\\n\",\n        \"output\": \" CC(=O)Nc1ccc(F)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Spironolactone\\n\",\n        \"output\": \" CC(=O)SC4CC1=CC(=O)CCC1(C)C5CCC2(C)C(CCC23CCC(=O)O3)C45\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H8BrCl2O3PS/c1-12-15(16,13-2)14-8-4-6(10)5(9)3-7(8)11/h3-4H,1-2H3\\n\",\n        \"output\": \" -6.09\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,7-phenantroline\\n\",\n        \"output\": \" [C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCOC=O\\n\",\n        \"output\": \" Propyl formate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Estradiol\\n\",\n        \"output\": \" 9.332543007969906e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Thiometon\\n\",\n        \"output\": \" CCSCCSP(=S)(OC)OC\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Fc1cccc(Br)c1\\n\",\n        \"output\": \" -2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C22H14/c1-3-7-17-15(5-1)9-11-21-19(17)13-14-20-18-8-4-2-6-16(18)10-12-22(20)21/h1-14H\\n\",\n        \"output\": \" Picene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" o-Aminophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Pentyl propanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Tetrafluthrin\\n\",\n        \"output\": \" InChI=1S/C17H14ClF7O2/c1-6-11(19)13(21)7(14(22)12(6)20)5-27-15(26)10-8(16(10,2)3)4-9(18)17(23,24)25/h4,8,10H,5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(9)5(10)2-3/h1-2,10H\\n\",\n        \"output\": \" 2,3,5-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H6S2/c1-3-4-2/h1-2H3\\n\",\n        \"output\": \" Dimethyldisulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 4-Chloroanisole\\n\",\n        \"output\": \" InChI=1S/C7H7ClO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)OC(=O)Nc1cccc(Cl)c1\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H13N3O3S/c1-8-7(12)13-9-5(14-4)6(11)10(2)3/h1-4H3,(H,8,12)\\n\",\n        \"output\": \" 0.106\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(C)(C)O\\n\",\n        \"output\": \" 2-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=O]\\n\",\n        \"output\": \" 9.332543007969906e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccccc1C(O)c2ccccc2\\n\",\n        \"output\": \" -2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H6N4O3S/c11-5-7-1-2-9(5)6-8-3-4(14-6)10(12)13/h3H,1-2H2,(H,7,11)\\n\",\n        \"output\": \" 0.0006025595860743575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Diisopropylsulfide\\n\",\n        \"output\": \" InChI=1S/C6H14S/c1-5(2)7-6(3)4/h5-6H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-6(2)7(3,4)5/h6H,1-5H3\\n\",\n        \"output\": \" 4.3651583224016566e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methyl acetate\\n\",\n        \"output\": \" InChI=1S/C3H6O2/c1-3(4)5-2/h1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][NH1][N][=N][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" Benzotriazole\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][S][C][=Branch1][C][=S][N][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" 1.3803842646028839e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3-Methyl-2-butanol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Pentene \\n\",\n        \"output\": \" CCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch1][N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][Ring1][=N][=Branch1][C][=O][=O][C][=C][Ring2][Ring1][Ring1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" -3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Isofenphos\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][N][C][Branch1][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Diallate\\n\",\n        \"output\": \" -4.2860000000000005\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" o-Chloronitrobenzene\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCCCCCC(=O)OC\\n\",\n        \"output\": \" 2.0417379446695274e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 3-Pentanone\\n\",\n        \"output\": \" 0.5248074602497725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" Pentachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its oil solubility expressed as a logarithm in mol/L. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)CCC)CC=C\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2-Chlorobiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 5,6-Dimethylchrysene\\n\",\n        \"output\": \" [C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CNC(=O)C(C)SCCSP(=O)(OC)(OC)\\n\",\n        \"output\": \" vamidothion\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-isoPrbarbital\\n\",\n        \"output\": \" InChI=1S/C12H18N2O3/c1-7(2)5-6-12(8(3)4)9(15)13-11(17)14-10(12)16/h5,8H,6H2,1-4H3,(H2,13,14,15,16,17)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3\\n\",\n        \"output\": \" Menthone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2\\n\",\n        \"output\": \" 0.36307805477010135 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C]\\n\",\n        \"output\": \" Ethylene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-3-9-7-5-4-6-8(9)2/h4-7H,3H2,1-2H3\\n\",\n        \"output\": \" 0.0006165950018614823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C27H42O3/c1-16-9-22-23(29-15-16)14-27(4)24(30-22)12-21-20-11-18-10-19(28)6-7-25(18,2)13-17(20)5-8-26(21,27)3/h11,16-17,19-24,28H,5-10,12-15H2,1-4H3\\n\",\n        \"output\": \" -7.32\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1ccc2cc3c4cccc5cccc(c3cc2c1)c45\\n\",\n        \"output\": \" -8.49\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2,4-Trichlorobenzene\\n\",\n        \"output\": \" Clc1ccc(Cl)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H16O/c1-3-5-6-8(4-2)7-9/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 0.007413102413009177 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=N(=O)c1cccc2ccccc12\\n\",\n        \"output\": \" 1-Nitronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCNc1ccccc1\\n\",\n        \"output\": \" -1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][=Branch1][=C][Ring1][#Branch2][Ring1][=C]\\n\",\n        \"output\": \" 1.5848931924611143e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H8O2/c1-4-3-5-2/h3H2,1-2H3\\n\",\n        \"output\": \" Dimethoxymethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Isoprocarb\\n\",\n        \"output\": \" CNC(=O)Oc1ccccc1C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 5-Methyl-5-ethylbarbituric acid\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(C)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" 3-Hexyne\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-6(2)5-7(3)4/h6-7H,5H2,1-4H3\\n\",\n        \"output\": \" -4.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C(C)(C)C\\n\",\n        \"output\": \" 2,2,3-Trimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" Pentachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" CCC(C)CCO\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Diazepam\\n\",\n        \"output\": \" CN2C(=O)CN=C(c1ccccc1)c3cc(Cl)ccc23\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" salicylanilide\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)\\n\",\n        \"output\": \" 0.00013182567385564074 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Brc1ccc(Br)cc1\\n\",\n        \"output\": \" 1,4-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H28O3/c1-4-22(25-14(2)23)12-10-20-19-7-5-15-13-16(24)6-8-17(15)18(19)9-11-21(20,22)3/h1,13,17-20H,5-12H2,2-3H3\\n\",\n        \"output\": \" norethindrone acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H4N2/c1-2-4-6-5-3-1/h1-4H\\n\",\n        \"output\": \" 12.589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H3N3O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H\\n\",\n        \"output\": \" 1,3,5-Trinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0001761976046411631 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Clc1ccc(CN(C2CCCC2)C(=O)Nc3ccccc3)cc1\\n\",\n        \"output\": \" Pencycuron\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCOC\\n\",\n        \"output\": \" 0.10232929922807542 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][S][Branch1][C][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2,2-Dimethyl-1-butanol\\n\",\n        \"output\": \" 0.09120108393559097 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Napthalene\\n\",\n        \"output\": \" InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Methylcyclohexene \\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 0.006165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H7I/c1-3(2)4/h3H,1-2H3\\n\",\n        \"output\": \" 2-Iodopropane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-5-3-2-4-6-5/h5H,2-4H2,1H3\\n\",\n        \"output\": \" 2-Methyltetrahydrofurane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H3\\n\",\n        \"output\": \" 2-Heptanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CSc1nnc(c(=O)n1N)C(C)(C)C\\n\",\n        \"output\": \" Metribuzin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=Branch1][C][=S][N][C][C]\\n\",\n        \"output\": \" 1,3-diethylthiourea\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\\n\",\n        \"output\": \" Nitramine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][Branch1][#Branch1][S][C][C][O][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc1ccc(Cl)cc1\\n\",\n        \"output\": \" 4-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCCCCl\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H14/c1-13-12-19-16-8-3-2-6-14(16)10-11-18(19)17-9-5-4-7-15(13)17/h2-12H,1H3\\n\",\n        \"output\": \" 6-Methylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1ccccc1C(O)C(O)c2ccccc2\\n\",\n        \"output\": \" hydrobenzoin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-2-4(8)6(10)5(3)9/h1-2,10H\\n\",\n        \"output\": \" 0.0022908676527677724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 1-Hexene\\n\",\n        \"output\": \" 0.0005888436553555889 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" m-Nitroaniline\\n\",\n        \"output\": \" Nc1cccc(c1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Camphor\\n\",\n        \"output\": \" InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][Branch1][P][C][=Branch1][C][=O][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][Cl][C][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring1][N][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" 5.508076964054041e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" 0.001435489433353656 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Phenylhydrazine\\n\",\n        \"output\": \" InChI=1S/C6H8N2/c7-8-6-4-2-1-3-5-6/h1-5,8H,7H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Ic1ccccc1\\n\",\n        \"output\": \" 0.000977237220955811 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Propyl propanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.0005011872336272725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCI\\n\",\n        \"output\": \" 0.005128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-6-7(3,8)5-2/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" 3-Methyl-3-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methyl-3-pentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-4-6(7)5(2)3/h5-7H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C16H34/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3-16H2,1-2H3\\n\",\n        \"output\": \" -8.4\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COc2cnc1cncnc1n2\\n\",\n        \"output\": \" 7-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccc2cc3ccccc3cc2c1\\n\",\n        \"output\": \" 2-Methylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Pentanol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-3-5(6)4-2/h5-6H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][=C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][#Branch1][C][=C][Ring1][O]\\n\",\n        \"output\": \" 0.001169499391019871 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Pirimicarb\\n\",\n        \"output\": \" 0.011220184543019636 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3,3-Dimethyl-1-butanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-6(2,3)4-5-7/h7H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8840315031266056e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H10Cl2N2O/c1-13(2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\",\n        \"output\": \" Diuron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][=N][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 12.589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" 0.8128305161640993 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H16N2O2/c1-8-7-9(15-11(14)12-2)5-6-10(8)13(3)4/h5-7H,1-4H3,(H,12,14)\\n\",\n        \"output\": \" Aminocarb\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OC4=C(C1CCC(CC1)c2ccc(Cl)cc2)C(=O)c3ccccc3C4=O\\n\",\n        \"output\": \" Atovaquone(0,430mg/ml) - neutral\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methyl octanoate\\n\",\n        \"output\": \" CCCCCCCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][N][Branch1][=Branch2][C][O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.907\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Ethylbutanal\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-3-6(4-2)5-7/h5-6H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C21H30O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12,16-19H,4-11H2,1-3H3\\n\",\n        \"output\": \" -4.42\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-hydroxypteridine\\n\",\n        \"output\": \" Oc2ncc1nccnc1n2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-3-5(6)4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" 3-Pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 9-Methylanthracene\\n\",\n        \"output\": \" InChI=1S/C15H12/c1-11-14-8-4-2-6-12(14)10-13-7-3-5-9-15(11)13/h2-10H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Sc1ccccc1\\n\",\n        \"output\": \" Thiophenol \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/CH2BrCl/c2-1-3/h1H2\\n\",\n        \"output\": \" Bromochloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCNP(=S)(OC)OC(=CC(=O)OC(C)C)C\\n\",\n        \"output\": \" -3.408\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCNc1nc(Cl)nc(NC(C)(C)C#N)n1\\n\",\n        \"output\": \" Cyanazine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC45CCC2C(CCC3CC1SC1CC23C)C4CCC5O\\n\",\n        \"output\": \" 3.890451449942805e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CN1CC(O)N(C1=O)c2nnc(s2)C(C)(C)C\\n\",\n        \"output\": \" 0.013273944577297402 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][#C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 3.3884415613920275e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Fc1ccc(F)cc1\\n\",\n        \"output\": \" 1,4-Difluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCc1ccccc1\\n\",\n        \"output\": \" Ethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H8N2O3/c1-6(2)3(9)7-5(11)8-4(6)10/h1-2H3,(H2,7,8,9,10,11)\\n\",\n        \"output\": \" 5,5-Dimethylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" kebuzone\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Propylene\\n\",\n        \"output\": \" InChI=1S/C3H6/c1-3-2/h3H,1H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C18H34O4/c1-3-5-15-21-17(19)13-11-9-7-8-10-12-14-18(20)22-16-6-4-2/h3-16H2,1-2H3\\n\",\n        \"output\": \" -3.8960000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][#Branch2][C]\\n\",\n        \"output\": \" -5.23\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Bibenzyl \\n\",\n        \"output\": \" InChI=1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1CC2C3CCC(O)(C(=O)C)C3(C)CC(O)C2(F)C4(C)C=CC(=O)C=C14\\n\",\n        \"output\": \" Fluoromethalone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Fluoroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" OCC(O)C(O)C(O)C(O)CO\\n\",\n        \"output\": \" 12.302687708123818 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H16/c1-11(2,3)9-10-7-5-4-6-8-10/h4-8H,9H2,1-3H3\\n\",\n        \"output\": \" t-Pentylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc1ccccc1Cl\\n\",\n        \"output\": \" 2-Chlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Nc1ccc(cc1)S(N)(=O)=O\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" p-Chloroiodobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H19O2PS3/c1-4-9-11(12,10-5-2)14-8-7-13-6-3/h4-8H2,1-3H3\\n\",\n        \"output\": \" 5.888436553555884e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H16N2O2/c1-8-7-9(15-11(14)12-2)5-6-10(8)13(3)4/h5-7H,1-4H3,(H,12,14)\\n\",\n        \"output\": \" -2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Trichloromethane\\n\",\n        \"output\": \" InChI=1S/CHCl3/c2-1(3)4/h1H\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12N2O3/c12-6-9(4-2-1-3-5-9)7(13)11-8(14)10-6/h1-5H2,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" Cyclohexyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)CO\\n\",\n        \"output\": \" 1.2589254117941673 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C2H3Cl/c1-2-3/h2H,1H2\\n\",\n        \"output\": \" -1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" p-terphenyl\\n\",\n        \"output\": \" c1ccc(cc1)c2ccc(cc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" DDE\\n\",\n        \"output\": \" InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(=O)CCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" kebuzone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][#C]\\n\",\n        \"output\": \" 0.000977237220955811 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Pentachlorophenol\\n\",\n        \"output\": \" InChI=1S/C6HCl5O/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2H4Cl2/c1-2(3)4/h2H,1H3\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H10/c1-3-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" Butane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Pyridine\\n\",\n        \"output\": \" 5.7543993733715695 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" Altretamine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H\\n\",\n        \"output\": \" 0.1 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Methylphenanthrene\\n\",\n        \"output\": \" Cc1cccc2c1ccc3ccccc32\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" o-Nitroanisole\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propylcyclopentane\\n\",\n        \"output\": \" CCCC1CCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C/C=C/C=O\\n\",\n        \"output\": \" t-Crotonaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4ClNO2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H\\n\",\n        \"output\": \" 0.001202264434617413 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Piperophos\\n\",\n        \"output\": \" CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)\\n\",\n        \"output\": \" rhodanine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C15H15ClN2O2/c1-18(2)15(19)17-12-5-9-14(10-6-12)20-13-7-3-11(16)4-8-13/h3-10H,1-2H3,(H,17,19)\\n\",\n        \"output\": \" 1.2882495516931348e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 0.0044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Diosgenin\\n\",\n        \"output\": \" InChI=1S/C27H42O3/c1-16-9-22-23(29-15-16)14-27(4)24(30-22)12-21-20-11-18-10-19(28)6-7-25(18,2)13-17(20)5-8-26(21,27)3/h11,16-17,19-24,28H,5-10,12-15H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Carbromal\\n\",\n        \"output\": \" CCC(Br)(CC)C(=O)NC(N)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Methyldymron\\n\",\n        \"output\": \" CN(C(=O)NC(C)(C)c1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Furfural\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(C)C1(CC=C)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" -2.016\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Triadimefon\\n\",\n        \"output\": \" InChI=1S/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Fenitrothion\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,3-Dimethylnaphthalene\\n\",\n        \"output\": \" Cc1cc(C)c2ccccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)CCO\\n\",\n        \"output\": \" 0.30902954325135906 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1,2,4,5-Tetramethylbenzene\\n\",\n        \"output\": \" -4.59\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Ethyl propionate\\n\",\n        \"output\": \" -0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Propyl propanoate\\n\",\n        \"output\": \" CCCCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Hexachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOc1ccc(cc1)C(C)(C)COCc3cccc(Oc2ccccc2)c3\\n\",\n        \"output\": \" Etofenprox\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][O]\\n\",\n        \"output\": \" 4-Methylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 3-Methyl-2-butanone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C15H15ClN2O4S/c1-8-4-3-5-9(2)14(8)18-15(20)10-6-13(23(17,21)22)11(16)7-12(10)19/h3-7,19H,1-2H3,(H,18,20)(H2,17,21,22)\\n\",\n        \"output\": \" -3.79\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H\\n\",\n        \"output\": \" Isoquinoline\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" m-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H\\n\",\n        \"output\": \" -3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Chloropham\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" 2-Methylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H30O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h12,16-18,24H,4-11H2,1-3H3\\n\",\n        \"output\": \" Hydroxyprogesterone-17a\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Fluvalinate\\n\",\n        \"output\": \" 9.931160484209335e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 0.5128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H18O2/c1-3-5-6-7-8-9(10)11-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" 0.0018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12)\\n\",\n        \"output\": \" Phenacetin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H4Cl6/c13-5-1-2-8(14)6(3-5)7-4-9(15)11(17)12(18)10(7)16/h1-4H\\n\",\n        \"output\": \" -7.68\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H3Cl7/c13-4-1-2-5(6(14)3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\\n\",\n        \"output\": \" 1.202264434617413e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methylpentane\\n\",\n        \"output\": \" CCCC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Fluorobenzene\\n\",\n        \"output\": \" Fc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][O]\\n\",\n        \"output\": \" Glycerol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Tricresyl phosphate\\n\",\n        \"output\": \" Cc1ccc(OP(=O)(Oc2cccc(C)c2)Oc3ccccc3C)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Etoposide (148-167,25mg/ml)\\n\",\n        \"output\": \" 0.0002685344445658506 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" COc2cnc1cncnc1n2\\n\",\n        \"output\": \" 0.12302687708123815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-5-3-8-12-10(2)6-4-7-11(9)12/h3-8H,1-2H3\\n\",\n        \"output\": \" 1,5-Dimethlnapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Azintamide\\n\",\n        \"output\": \" CCN(CC)C(=O)CSc1ccc(Cl)nn1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C2Cl2F4/c3-1(5,6)2(4,7)8\\n\",\n        \"output\": \" 1,2-Dichlorotetrafluoroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-7-11-5-3-4-6-12(11)8-10(9)2/h3-8H,1-2H3\\n\",\n        \"output\": \" -4.72\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Hexene\\n\",\n        \"output\": \" [C][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" m-Chloroiodobenzene\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Carbanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCC=C\\n\",\n        \"output\": \" 3.090295432513592e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Picene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Phenylmethanol\\n\",\n        \"output\": \" 0.3981071705534972 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C2NC(=O)C1(CCCC1)C(=O)N2\\n\",\n        \"output\": \" 0.004477133041763623 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][C][C][Ring1][S][=C][Ring1][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.6558609352295814e-10 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" COc1ccccc1O\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Phenylphenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" p-Nitroanisole\\n\",\n        \"output\": \" -2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Pteridine\\n\",\n        \"output\": \" 1.0471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-2-4(10)6(9)5(3)8/h1-2,10H\\n\",\n        \"output\": \" 2,3,4-Trichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,3-diethylthiourea\\n\",\n        \"output\": \" CCNC(=S)NCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC45CCC2C(CCC3CC1SC1CC23C)C4CCC5O\\n\",\n        \"output\": \" Epitostanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Sorbitol\\n\",\n        \"output\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2\\n\",\n        \"output\": \" -4.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Benzaldehyde\\n\",\n        \"output\": \" 0.06456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Terbufos\\n\",\n        \"output\": \" InChI=1S/C9H21O2PS3/c1-6-10-12(13,11-7-2)15-8-14-9(3,4)5/h6-8H2,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H4ClI/c7-5-1-3-6(8)4-2-5/h1-4H\\n\",\n        \"output\": \" 9.332543007969905e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O][C][Branch1][C][N][=O]\\n\",\n        \"output\": \" 0.10351421666793438 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(C=Nc1ccc(C)cc1C)C=Nc2ccc(C)cc2C\\n\",\n        \"output\": \" Amitraz\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methylcyclohexane \\n\",\n        \"output\": \" InChI=1S/C7H14/c1-7-5-3-2-4-6-7/h7H,2-6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H\\n\",\n        \"output\": \" p-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H\\n\",\n        \"output\": \" 0.000630957344480193 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H26O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-16H,3-10H2,1-2H3\\n\",\n        \"output\": \" 0.00020417379446695296 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" o-Nitroaniline\\n\",\n        \"output\": \" InChI=1S/C6H6N2O2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H,7H2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" o-Nitroanisole\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Pencycuron\\n\",\n        \"output\": \" -5.915\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" borneol\\n\",\n        \"output\": \" 0.004786300923226385 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0001174897554939529 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2\\n\",\n        \"output\": \" Phenylmethanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" -8.4\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.863\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dicofol\\n\",\n        \"output\": \" OC(c1ccc(Cl)cc1)(c2ccc(Cl)cc2)C(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Bromophos\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Chloropicrin\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1,2-Dibromobenzene\\n\",\n        \"output\": \" 0.00031622776601683794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCN(Cc1c(F)cccc1Cl)c2c(cc(cc2N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" Flumetralin\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-3-4-5(2)6/h3-4H2,1-2H3\\n\",\n        \"output\": \" -0.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCS\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" -5.24\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCC1(CC)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" Butethal\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,3-Dimethylbutane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N][C][C][O][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N]\\n\",\n        \"output\": \" 1.9952623149688786e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCOCCC\\n\",\n        \"output\": \" Dipropyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-6(2,3)4-5-7/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" 3,3-Dimethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" norflurazon\\n\",\n        \"output\": \" CNc2cnn(c1cccc(c1)C(F)(F)F)c(=O)c2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\\n\",\n        \"output\": \" p-benzidine\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Risocaine\\n\",\n        \"output\": \" InChI=1S/C10H13NO2/c1-2-7-13-10(12)8-3-5-9(11)6-4-8/h3-6H,2,7,11H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H\\n\",\n        \"output\": \" -9.332\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C\\n\",\n        \"output\": \" Methoprene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Acetophenone\\n\",\n        \"output\": \" InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H10/c1-4(2)3/h4H,1-3H3\\n\",\n        \"output\": \" -2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H12O6/c17-10-2-1-8-13-9-4-12(19)11(18)3-7(9)5-16(13,21)6-22-15(8)14(10)20/h1-4,17,19-21H,5-6H2\\n\",\n        \"output\": \" hematein\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=N][C][=Branch1][C][=O][NH1][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 0.10665961212302578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H8O/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\\n\",\n        \"output\": \" -4.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Flucythrinate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][C][=C][Branch1][#Branch1][O][C][Branch1][C][F][F][C][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chlorothalonil\\n\",\n        \"output\": \" InChI=1S/C8Cl4N2/c9-5-3(1-13)6(10)8(12)7(11)4(5)2-14\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 6-Methylchrysene\\n\",\n        \"output\": \" InChI=1S/C19H14/c1-13-12-19-16-8-3-2-6-14(16)10-11-18(19)17-9-5-4-7-15(13)17/h2-12H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H12NO5PS/c1-7-6-8(4-5-9(7)10(11)12)15-16(17,13-2)14-3/h4-6H,1-3H3\\n\",\n        \"output\": \" -4.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Branch1][C][Br][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.1622776601683795e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C20H30N2O5S/c1-7-25-17(23)11-12-22(14(2)3)28-21(6)19(24)26-16-10-8-9-15-13-20(4,5)27-18(15)16/h8-10,14H,7,11-13H2,1-6H3\\n\",\n        \"output\": \" 1.9498445997580456e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H16O/c9-8-6-4-2-1-3-5-7-8/h8-9H,1-7H2\\n\",\n        \"output\": \" 0.05128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2,4-Dichlorophenol \\n\",\n        \"output\": \" -1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H19ClNO3PS2/c1-10(2)15(12-7-5-11(14)6-8-12)13(16)9-21-19(20,17-3)18-4/h5-8,10H,9H2,1-4H3\\n\",\n        \"output\": \" -4.4319999999999995\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 5-Allyl-5-ethylbarbital\\n\",\n        \"output\": \" -1.614\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Prednisolone\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Phorate\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCC=O\\n\",\n        \"output\": \" 0.9772372209558107 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3\\n\",\n        \"output\": \" Corticosterone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(C)C(=O)C\\n\",\n        \"output\": \" 3-Methyl-2-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H6N4O/c1-12-7-10-4-5-6(11-7)9-3-2-8-5/h2-4H,1H3\\n\",\n        \"output\": \" -1.11\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methylparaben\\n\",\n        \"output\": \" COC(=O)c1ccc(O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Monolinuron\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3H,1,4-10H2,2H3\\n\",\n        \"output\": \" 1-Decene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Malonic acid diethylester\\n\",\n        \"output\": \" CCOC(=O)CC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CNN\\n\",\n        \"output\": \" 21.87761623949553 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,2-Dimethylpentanol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Tetradecanol\\n\",\n        \"output\": \" CCCCCCCCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][Branch1][C][N][=O][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" -2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCOc1ccccc1\\n\",\n        \"output\": \" 0.004677351412871981 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCC(C)(C)C\\n\",\n        \"output\": \" 2,2-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 5-Ethyl-5-isopropylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=O]\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H14O5/c1-18-8-5-10(16)13-12(6-8)19-11-3-2-7(15)4-9(11)14(13)17/h2-6,9,11-13,15-16H,1H3\\n\",\n        \"output\": \" -2.943\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Ethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2\\n\",\n        \"output\": \" 0.0025703957827688645 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccc(Cl)cc1\\n\",\n        \"output\": \" -3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dimethyl sulfide\\n\",\n        \"output\": \" CSC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" COC(=O)Nc1cccc(OC(=O)Nc2cccc(C)c2)c1\\n\",\n        \"output\": \" -4.805\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H9Cl2NO/c1-2-9(13)12-6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3,(H,12,13)\\n\",\n        \"output\": \" 0.001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Iodopropane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][I]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc1ccc(O)cc1\\n\",\n        \"output\": \" p-Aminophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)\\n\",\n        \"output\": \" 0.003944573020752785 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H\\n\",\n        \"output\": \" Triphenylene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,3-Dimethylpentane\\n\",\n        \"output\": \" CCC(C)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][O]\\n\",\n        \"output\": \" 1-Propanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Inosine\\n\",\n        \"output\": \" [O][C][C][O][C][Branch1][=Branch2][C][Branch1][C][O][C][Ring1][=Branch1][O][N][C][=N][C][=C][Branch1][C][O][N][=C][N][=C][Ring1][#Branch2][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H14O4/c1-3-15-11(13)9-7-5-6-8-10(9)12(14)16-4-2/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Brc1ccccc1\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Cc1ccc(cc1)c2ccccc2\\n\",\n        \"output\": \" 2.39883291901949e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Dimethyl phthalate\\n\",\n        \"output\": \" -1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-4-3-5-8-7(6)2/h3-5H,1-2H3\\n\",\n        \"output\": \" 2.3988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=C]\\n\",\n        \"output\": \" 1-Pentene \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H10Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8,13-14H\\n\",\n        \"output\": \" DDD\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 2-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 5-Allyl-5-isopropylbarbital\\n\",\n        \"output\": \" 0.01958844673505989 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][S][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" Simetryn\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Quinoline\\n\",\n        \"output\": \" c1ccc2ncccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H3\\n\",\n        \"output\": \" 1-Nonyne \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Fc1cccc(F)c1C(=O)NC(=O)Nc2ccc(Cl)cc2\\n\",\n        \"output\": \" 9.549925860214369e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][=C][Branch1][C][C][N][=C][Branch1][Ring2][N][C][C][NH1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" Ethirimol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Triazolam\\n\",\n        \"output\": \" -4.09\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 7,12-Dimethylbenz(a)anthracene\\n\",\n        \"output\": \" Cc1c2ccccc2c(C)c3ccc4ccccc4c13\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Propazine\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Nc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" -2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H\\n\",\n        \"output\": \" Benzaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Chlorotoluron\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H7ClO/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3\\n\",\n        \"output\": \" -2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.0001191242008027375 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=S][NH1][Ring1][Branch2]\\n\",\n        \"output\": \" -2.436\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][Branch1][C][C][O][C][C]\\n\",\n        \"output\": \" 1,1-Diethoxyethane \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" BrC(Cl)Cl\\n\",\n        \"output\": \" Bromodichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,4-Dinitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4N2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" salicylanilide\\n\",\n        \"output\": \" -3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Diisopropyl ether \\n\",\n        \"output\": \" CC(C)OC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Ethirimol\\n\",\n        \"output\": \" -3.028\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=C][C][=Branch1][C][=O][NH1][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 1-methyluracil\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Naled\\n\",\n        \"output\": \" InChI=1S/C4H7Br2Cl2O4P/c1-10-13(9,11-2)12-3(5)4(6,7)8/h3H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\\n\",\n        \"output\": \" -5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H14/c1-7-5-3-2-4-6-7/h7H,2-6H2,1H3\\n\",\n        \"output\": \" 0.0001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Difenoxuron\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][C][=C][Ring2][Ring1][Ring1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Phenylethanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12N4O3/c17-11(14-8-10-4-2-1-3-5-10)9-15-7-6-13-12(15)16(18)19/h1-7H,8-9H2,(H,14,17)\\n\",\n        \"output\": \" Benznidazole\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,4-Dimethylpentane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,4-Dimethylpyridine\\n\",\n        \"output\": \" [C][C][=C][C][=N][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=O][Branch1][Ring2][O][C][C][O][C][C]\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H12/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3\\n\",\n        \"output\": \" 0.00042657951880159257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][S][C][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.00011830415557251647 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Succinimide\\n\",\n        \"output\": \" O=C1CCC(=O)N1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#Branch1]\\n\",\n        \"output\": \" Diazepam\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Octadecanol\\n\",\n        \"output\": \" InChI=1S/C18H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h19H,2-18H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,3-Dimethylpentane\\n\",\n        \"output\": \" InChI=1S/C7H16/c1-5-7(4)6(2)3/h6-7H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H7Br/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\\n\",\n        \"output\": \" 4-Bromotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)C1CCC(C)CC1=O\\n\",\n        \"output\": \" Menthone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" t-Crotonaldehyde\\n\",\n        \"output\": \" 2.0892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 2-Ethyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Barbital\\n\",\n        \"output\": \" InChI=1S/C8H12N2O3/c1-3-8(4-2)5(11)9-7(13)10-6(8)12/h3-4H2,1-2H3,(H2,9,10,11,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Lenacil\\n\",\n        \"output\": \" [O][=C][NH1][C][C][C][C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][#Branch2][C][C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Amobarbital\\n\",\n        \"output\": \" [C][C][C][Branch1][Branch2][C][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=N][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][N][=C][N][Ring1][Branch1][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Etomidate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCCCC(=O)OCC\\n\",\n        \"output\": \" -3.39\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Testosterone\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2,2',3,3',4,4',5,5'-PCB\\n\",\n        \"output\": \" 6.918309709189363e-10 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2,6-Dimethylnaphthalene \\n\",\n        \"output\": \" -4.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N]\\n\",\n        \"output\": \" o-Toluidine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)=CCCC(C)=CC(=O)\\n\",\n        \"output\": \" citral\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.22\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Chrysene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H9ClNO5PS/c1-13-16(17,14-2)15-8-4-3-6(10(11)12)5-7(8)9/h3-5H,1-2H3\\n\",\n        \"output\": \" Dicapthon\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][=C][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" -3.67\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" Cycloheptene\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-3-5-7(8)6-4-2/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 4-Heptanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OCc2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" Permethrin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" OC(c1ccc(Cl)cc1)(c2ccc(Cl)cc2)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" 2.1577444091526647e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Acetonitrile\\n\",\n        \"output\": \" InChI=1S/C2H3N/c1-2-3/h1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Pentyl acetate\\n\",\n        \"output\": \" [C][C][C][C][C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3/c7-4-2-1-3-5(8)6(4)9/h1-3H\\n\",\n        \"output\": \" 1,2,3-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H14O/c8-7-5-3-1-2-4-6-7/h7-8H,1-6H2\\n\",\n        \"output\": \" Cycloheptanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc1cc(C)nc(n1)C(C)C\\n\",\n        \"output\": \" Diazinon\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" Pentachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 1,3,5-Tribromobenzene\\n\",\n        \"output\": \" 2.5118864315095823e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCC=O\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Methylbutanol\\n\",\n        \"output\": \" -0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring2][Ring1][Ring1][Ring1][S][C]\\n\",\n        \"output\": \" 3.8018939632056124e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=O]\\n\",\n        \"output\": \" Propionaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanone\\n\",\n        \"output\": \" CC(C)C(=O)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCI\\n\",\n        \"output\": \" 1-Iodopropane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)O\\n\",\n        \"output\": \" 2-Propanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H10/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h1-10H\\n\",\n        \"output\": \" Pyrene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C][=C]\\n\",\n        \"output\": \" 5-Allyl-5-methylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" c2cnc1ncncc1n2\\n\",\n        \"output\": \" 1.0471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Methyl pentanoate\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Pentanone\\n\",\n        \"output\": \" CCC(=O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,4-Dimethylpentane\\n\",\n        \"output\": \" InChI=1S/C7H16/c1-6(2)5-7(3)4/h6-7H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,2,3-Trimethylbenzene \\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Cl)C(Cl)Cl\\n\",\n        \"output\": \" 1,1,2,2-Tetrachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCOCCOCC\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H23NOS/c1-6-14-11(13)12(7-9(2)3)8-10(4)5/h9-10H,6-8H2,1-5H3\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" p-Aminophenol\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1=CCC(CC1)C(C)=C\\n\",\n        \"output\": \" d-Limonene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H14NO5PS/c1-3-14-17(18,15-4-2)16-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" Parathion\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" Ethofumesate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 4-Methylbiphenyl\\n\",\n        \"output\": \" Cc1ccc(cc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Hexanone\\n\",\n        \"output\": \" 0.14791083881682077 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Aminocarb\\n\",\n        \"output\": \" InChI=1S/C11H16N2O2/c1-8-7-9(15-11(14)12-2)5-6-10(8)13(3)4/h5-7H,1-4H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fenitrothion\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1,2-Dibromoethane\\n\",\n        \"output\": \" -1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][C]\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H16O/c9-8-6-4-2-1-3-5-7-8/h8-9H,1-7H2\\n\",\n        \"output\": \" Cyclooctanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][=C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 0.007943282347242814 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Isoproturon\\n\",\n        \"output\": \" CC(C)c1ccc(NC(=O)N(C)C)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2,6-Dimethylpyridine\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-3-4-8(9)7(2)5-6/h3-5,9H,1-2H3\\n\",\n        \"output\": \" 2,4-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)\\n\",\n        \"output\": \" 0.0588843655355589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COCOC\\n\",\n        \"output\": \" Dimethoxymethane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CH3NO2/c1-2(3)4/h1H3\\n\",\n        \"output\": \" 1.8197008586099834 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,3-Benzenediol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2,3,5-Tetrachlorobenzene\\n\",\n        \"output\": \" Clc1cc(Cl)c(Cl)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 2-Methylbutanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Terbacil\\n\",\n        \"output\": \" -2.484\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][I]\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Phorate\\n\",\n        \"output\": \" CCOP(=S)(OCC)SCSCC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H\\n\",\n        \"output\": \" p-Hydroxybenzaldehyde \\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dieldrin\\n\",\n        \"output\": \" ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H11NO2/c15-12-9-5-4-8-11(12)13(16)14-10-6-2-1-3-7-10/h1-9,15H,(H,14,16)\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methylpropene\\n\",\n        \"output\": \" [C][C][=Branch1][C][=C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)OC=O\\n\",\n        \"output\": \" -0.63\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Phenmedipham\\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][=C][Ring1][P]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ditalimfos\\n\",\n        \"output\": \" InChI=1S/C12H14NO4PS/c1-3-16-18(19,17-4-2)13-11(14)9-7-5-6-8-10(9)12(13)15/h5-8H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][Ring1][=C]\\n\",\n        \"output\": \" Picene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methylcyclohexane \\n\",\n        \"output\": \" [C][C][C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,2',3,3',4,4',5,5'-PCB\\n\",\n        \"output\": \" [Cl][C][=C][C][=Branch1][=N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COc1ccc(NC(=O)N(C)C)cc1Cl\\n\",\n        \"output\": \" Metoxuron\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pentachlorophenol\\n\",\n        \"output\": \" [O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][I][C][=C][Branch1][Ring1][C][#N][C][=C][Ring1][=Branch2][I]\\n\",\n        \"output\": \" 0.0002454708915685031 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-8-15-13(5-1)11-12-17-16-9-3-6-14-7-4-10-18(19(14)16)20(15)17/h1-12H\\n\",\n        \"output\": \" Benzo(j)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H19Br2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\",\n        \"output\": \" Deltamethrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Nonanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C2H6S/c1-2-3/h3H,2H2,1H3\\n\",\n        \"output\": \" -0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(SC)c(C)c1\\n\",\n        \"output\": \" Fenthion\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Fluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Acetamide\\n\",\n        \"output\": \" InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Bibenzyl \\n\",\n        \"output\": \" [C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,4,6-Trichlorophenol\\n\",\n        \"output\": \" [O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methylanthracene\\n\",\n        \"output\": \" InChI=1S/C15H12/c1-11-6-7-14-9-12-4-2-3-5-13(12)10-15(14)8-11/h2-10H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Metoxuron\\n\",\n        \"output\": \" COc1ccc(NC(=O)N(C)C)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1cccc(N)c1\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2\\n\",\n        \"output\": \" Indan\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Butylate\\n\",\n        \"output\": \" [C][C][S][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Raffinose\\n\",\n        \"output\": \" InChI=1S/C18H32O16/c19-1-5-8(22)11(25)13(27)16(31-5)30-3-7-9(23)12(26)14(28)17(32-7)34-18(4-21)15(29)10(24)6(2-20)33-18/h5-17,19-29H,1-4H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCI\\n\",\n        \"output\": \" 1-Iodoheptane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Octadecanol\\n\",\n        \"output\": \" -8.4\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Propylbenzene \\n\",\n        \"output\": \" InChI=1S/C9H12/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Bromomethane\\n\",\n        \"output\": \" 0.16218100973589297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CNC(=O)C=C(C)OP(=O)(OC)OC\\n\",\n        \"output\": \" Azodrin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][N][=C][Branch1][C][Cl][N][Branch1][Ring2][N][=Ring1][=Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.00021978598727848253 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2-Dichloropropane\\n\",\n        \"output\": \" [C][C][Branch1][C][Cl][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H15N5S/c1-12(2)6-9-7(13(3)4)11-8(10-6)14-5/h1-5H3\\n\",\n        \"output\": \" Simetryn\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H11N/c1-2-9-8-6-4-3-5-7-8/h3-7,9H,2H2,1H3\\n\",\n        \"output\": \" N-Ethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2\\n\",\n        \"output\": \" Aniline \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][C][=N][N][Branch2][Ring1][Ring1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][=Ring1][P][Cl]\\n\",\n        \"output\": \" norflurazon\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc2cnccc2c1\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cycluron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-6-4-2-3-5-7(6)8/h2-5,8H,1H3\\n\",\n        \"output\": \" 2-Methylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" COc1ccc(Cl)cc1\\n\",\n        \"output\": \" -2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1c(F)c(F)c(COC(=O)C2C(C=C(Cl)C(F)(F)F)C2(C)C)c(F)c1F\\n\",\n        \"output\": \" Tetrafluthrin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H3\\n\",\n        \"output\": \" 0.00016982436524617443 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" 0.001188502227437019 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H8O3/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5,9H,1H3\\n\",\n        \"output\": \" -1.827\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" OC(c1ccc(Cl)cc1)(c2cncnc2)c3ccccc3Cl\\n\",\n        \"output\": \" 4.168693834703355e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)C(=O)Nc2ccc(Oc1ccc(Cl)cc1)cc2\\n\",\n        \"output\": \" Chloroxuron\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" 2,3-Dimethyl-1,3-Butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccc(O)cc1\\n\",\n        \"output\": \" -0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H7ClO/c1-9-7-5-3-2-4-6(7)8/h2-5H,1H3\\n\",\n        \"output\": \" 2-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzo[ghi]perylene\\n\",\n        \"output\": \" c1cc2ccc3ccc4ccc5cccc6c(c1)c2c3c4c56\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 2,4,6-Trinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H14ClN3OS/c1-3-14(4-2)10(15)7-16-9-6-5-8(11)12-13-9/h5-6H,3-4,7H2,1-2H3\\n\",\n        \"output\": \" 0.019230917289101587 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(=O)N\\n\",\n        \"output\": \" Acetamide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Triethyl phosphate\\n\",\n        \"output\": \" InChI=1S/C6H15O4P/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,3-Difluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility of given compound in room temperature? ->\",\n        \"input\": \" 2-Propanol\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)\\n\",\n        \"output\": \" 0.004570881896148752 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" C/C1CCCCC1\\\\C\\n\",\n        \"output\": \" 5.011872336272725e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCO\\n\",\n        \"output\": \" 1-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Diphenylmethane\\n\",\n        \"output\": \" InChI=1S/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" O=C1CCC(=O)N1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1,2,4,5-Tetrachlorobenzene\\n\",\n        \"output\": \" -5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][=C][Branch1][#C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][I][C][=C][C][=C][Ring1][S]\\n\",\n        \"output\": \" 6.165950018614822e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(Cl)Cl\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-15,18,22,26H,3-8,10-11H2,1-2H3\\n\",\n        \"output\": \" Cortisone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Triadimefon\\n\",\n        \"output\": \" 0.0002454708915685031 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccoc1\\n\",\n        \"output\": \" Furane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H10/c1-9-5-4-7-10-6-2-3-8-11(9)10/h2-8H,1H3\\n\",\n        \"output\": \" 1-Methylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-4-5-6-7(8)9-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" 0.013489628825916533 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1cccc(Cl)c1Cl\\n\",\n        \"output\": \" 1,2,3-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC=C\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" m-Chloronitrobenzene \\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H26N2O4/c1-2-3-4-11-16-20(26)29-17-25-21(27)23(24-22(25)28,18-12-7-5-8-13-18)19-14-9-6-10-15-19/h5-10,12-15H,2-4,11,16-17H2,1H3,(H,24,28)\\n\",\n        \"output\": \" 3-Heptanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCOCCO\\n\",\n        \"output\": \" 2-Butoxyethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Butylate\\n\",\n        \"output\": \" CCSC(=O)N(CC(C)C)CC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H10S/c1-2-3-4-5/h5H,2-4H2,1H3\\n\",\n        \"output\": \" Butanethiol \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H19NO4/c1-2-20-17(19)18-12-13-21-14-8-10-16(11-9-14)22-15-6-4-3-5-7-15/h3-11H,2,12-13H2,1H3,(H,18,19)\\n\",\n        \"output\": \" Fenoxycarb\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Theophylline\\n\",\n        \"output\": \" InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch1][N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][Ring1][=N][=Branch1][C][=O][=O][C][=C][Ring2][Ring1][Ring1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" Bendroflumethiazide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3\\n\",\n        \"output\": \" methyl laurate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCC1(C(=O)NC(=O)NC1=O)C2=CCC3CCC2C3\\n\",\n        \"output\": \" -2.696\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H12ClNO2/c1-7(2)14-10(13)12-9-5-3-4-8(11)6-9/h3-7H,1-2H3,(H,12,13)\\n\",\n        \"output\": \" Chloropham\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][C][S][C][C]\\n\",\n        \"output\": \" 5.888436553555884e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCC(C)(C)CC\\n\",\n        \"output\": \" 5.888436553555884e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-4-5-6-9-7(2)8/h3-6H2,1-2H3\\n\",\n        \"output\": \" Pentyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][Branch1][Ring2][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][O][=O]\\n\",\n        \"output\": \" Talbutal\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=O)C3(C)CCC4C2C=C(C)C1=CC(=O)CCC1(C)C2CCC34C\\n\",\n        \"output\": \" Medrogestone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC(=O)C=Cc1ccccc1\\n\",\n        \"output\": \" ethyl cinnamate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c2ccc1[nH]ccc1c2\\n\",\n        \"output\": \" Indole\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Trichloromethane\\n\",\n        \"output\": \" 0.06760829753919818 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Fenthion\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][Ring1][S][C][C][Branch1][C][C][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O]\\n\",\n        \"output\": \" 2,6-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][=O]\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-Methylaniline \\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cc2c3ccccc3ccc2c4ccccc14\\n\",\n        \"output\": \" 6-Methylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Fluoranthene\\n\",\n        \"output\": \" c1ccc2c(c1)c3cccc4cccc2c34\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-3-4(2)5/h3H2,1-2H3\\n\",\n        \"output\": \" 2-Butanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" o-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC(=O)Nc1ccc(Br)cc1\\n\",\n        \"output\": \" 0.0008260379495771783 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][=N]\\n\",\n        \"output\": \" -3.239\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Butanethiol \\n\",\n        \"output\": \" CCCCS\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Fenitrothion\\n\",\n        \"output\": \" -4.04\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(C)O\\n\",\n        \"output\": \" 2-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,3-Dimethylnaphthalene\\n\",\n        \"output\": \" [C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Chloroethane\\n\",\n        \"output\": \" ClCC\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C17H12/c1-3-7-14-12(5-1)9-10-16-15-8-4-2-6-13(15)11-17(14)16/h1-10H,11H2\\n\",\n        \"output\": \" -6.68\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methyldymron\\n\",\n        \"output\": \" InChI=1S/C17H20N2O/c1-17(2,14-10-6-4-7-11-14)18-16(20)19(3)15-12-8-5-9-13-15/h4-13H,1-3H3,(H,18,20)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Barban\\n\",\n        \"output\": \" 4.265795188015926e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Antipyrene\\n\",\n        \"output\": \" InChI=1S/C11H12N2O/c1-9-8-11(14)13(12(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Octane\\n\",\n        \"output\": \" 5.754399373371567e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 4-Bromophenol\\n\",\n        \"output\": \" InChI=1S/C6H5BrO/c7-5-1-3-6(8)4-2-5/h1-4,8H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10Cl2F3NO/c13-5-7-6-18(11(19)10(7)14)9-3-1-2-8(4-9)12(15,16)17/h1-4,7,10H,5-6H2\\n\",\n        \"output\": \" Flurochloridone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CC(C)CCOC=O\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" -5.65\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,8-Cineole\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][O][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-4-6-7-8(3,9)5-2/h9H,4-7H2,1-3H3\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Amobarbital\\n\",\n        \"output\": \" 0.003404081897010009 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 7-methylpteridine\\n\",\n        \"output\": \" 0.13995873225726177 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCC#C\\n\",\n        \"output\": \" 1-Heptyne\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,1-Diethoxyethane \\n\",\n        \"output\": \" CCOC(C)OCC\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Butan-2-ol\\n\",\n        \"output\": \" InChI=1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Riboflavin\\n\",\n        \"output\": \" InChI=1S/C17H20N4O6/c1-7-3-9-10(4-8(7)2)21(5-11(23)14(25)12(24)6-22)15-13(18-9)16(26)20-17(27)19-15/h3-4,11-12,14,22-25H,5-6H2,1-2H3,(H,20,26,27)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Nonanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccccc1O\\n\",\n        \"output\": \" Phenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" O=C1N(COC(=O)CCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" -5.071000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Fenarimol\\n\",\n        \"output\": \" InChI=1S/C17H12Cl2N2O/c18-14-7-5-12(6-8-14)17(22,13-9-20-11-21-10-13)15-3-1-2-4-16(15)19/h1-11,22H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" m-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C(Nc1ccc(cc1Cl)C(F)(F)F)C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" Fluvalinate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3\\n\",\n        \"output\": \" 4-hexylresorcinol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCSCC\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=C][Ring1][#C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" -9.017999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cn2c(=O)on(c1ccc(Cl)c(Cl)c1)c2=O\\n\",\n        \"output\": \" Methazole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H13F2N3O/c17-13-7-5-12(6-8-13)16(22,9-21-11-19-10-20-21)14-3-1-2-4-15(14)18/h1-8,10-11,22H,9H2\\n\",\n        \"output\": \" Flutriafol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Fenitrothion\\n\",\n        \"output\": \" COP(=S)(OC)Oc1ccc(N(=O)=O)c(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Methyl-2-butanone\\n\",\n        \"output\": \" CC(C)C(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCC(C)CO\\n\",\n        \"output\": \" -0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=N(=O)c1c(Cl)c(Cl)ccc1\\n\",\n        \"output\": \" 2,3-Dichloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H5Cl/c1-2-3/h2H2,1H3\\n\",\n        \"output\": \" Chloroethane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0199526231496888 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H10Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8,13-14H\\n\",\n        \"output\": \" -7.2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H5I/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" Iodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,2,3-Trimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 3-Methyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][=Branch1][N][Branch1][C][C][C][C][Branch1][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.004365158322401661 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCN(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" Neburon\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H8N2O3/c10-4-7(2-1-3-7)5(11)9-6(12)8-4/h1-3H2,(H2,8,9,10,11,12)\\n\",\n        \"output\": \" 0.022130947096056376 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Nitrobenzene\\n\",\n        \"output\": \" O=N(=O)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(=O)c1ccccc1\\n\",\n        \"output\": \" 0.05248074602497726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cccc(C)c1O\\n\",\n        \"output\": \" 2,6-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,4-Dimethyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diethyl sulfide\\n\",\n        \"output\": \" [C][C][S][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3\\n\",\n        \"output\": \" 2.691534803926914e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H2Br4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\\n\",\n        \"output\": \" 1,2,4,5-Tetrabromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Nitramine\\n\",\n        \"output\": \" InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][C][Branch1][C][C][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Deltamethrin\\n\",\n        \"output\": \" CC1(C)C(C=C(Br)Br)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3\\n\",\n        \"output\": \" -5.84\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,1,2,2-Tetrachloroethane\\n\",\n        \"output\": \" ClC(Cl)C(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Methyl-1-Butene\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" OC1C(O)C(O)C(O)C(O)C1O\\n\",\n        \"output\": \" d-inositol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Equilenin\\n\",\n        \"output\": \" [C][C][C][C][C][=C][Branch1][S][C][=C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COc1nc(NC(C)C)nc(NC(C)C)n1\\n\",\n        \"output\": \" 0.0033265955329400436 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OCCCC=C\\n\",\n        \"output\": \" 4-Pentene-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,6-Dimethylphenol\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Hydroxybenzamide\\n\",\n        \"output\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" p-t-Butylphenol\\n\",\n        \"output\": \" 0.003890451449942805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Methyl decanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Benfluralin\\n\",\n        \"output\": \" CCCCN(CC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H10/c1-4(2)3/h4H,1-3H3\\n\",\n        \"output\": \" 2-Methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)C(=O)Nc1cccc(c1)C(F)(F)F\\n\",\n        \"output\": \" Fluorometuron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Chloropropane\\n\",\n        \"output\": \" 0.033884415613920256 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 4-Bromotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][C][C][=C][C][=C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H10S/c1-3-5-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" Diethyl sulfide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Fructose\\n\",\n        \"output\": \" OCC1OC(O)(CO)C(O)C1O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Propionitrile\\n\",\n        \"output\": \" InChI=1S/C3H5N/c1-2-3-4/h2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][C][C][=Branch1][C][=O][N][Ring1][=Branch1]\\n\",\n        \"output\": \" Succinimide\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][N][N][=C][C][Branch1][C][N][=C][Branch1][C][Br][C][Ring1][Branch2][=O]\\n\",\n        \"output\": \" 0.0007464487584100669 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Siduron\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Chlorophenol\\n\",\n        \"output\": \" Oc1ccccc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" o-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCOC=O\\n\",\n        \"output\": \" -1.37\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzoxazole\\n\",\n        \"output\": \" c2ccc1ocnc1c2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,2,3-Trimethylbutane\\n\",\n        \"output\": \" -4.36\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methylpentane\\n\",\n        \"output\": \" InChI=1S/C6H14/c1-4-5-6(2)3/h6H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOP(=S)(OCC)Oc1nc(Cl)n(n1)C(C)C\\n\",\n        \"output\": \" Isazofos\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H9Cl2NO3/c1-3-12(2)10(16)15(11(17)18-12)9-5-7(13)4-8(14)6-9/h3-6H,1H2,2H3\\n\",\n        \"output\": \" Vinclozolin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CSc1nc(NC(C)C)nc(NC(C)C)n1\\n\",\n        \"output\": \" Prometryn\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methyl formate\\n\",\n        \"output\": \" InChI=1S/C2H4O2/c1-4-2-3/h2H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2,4-Trimethylbenzene\\n\",\n        \"output\": \" InChI=1S/C9H12/c1-7-4-5-8(2)9(3)6-7/h4-6H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl benzoate \\n\",\n        \"output\": \" InChI=1S/C9H10O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSC(C)(C)C\\n\",\n        \"output\": \" Terbufos\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Hexestrol\\n\",\n        \"output\": \" 3.715352290971728e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\\n\",\n        \"output\": \" Benzocaine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-Nitrotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][=C][Ring1][P]\\n\",\n        \"output\": \" 1.5667510701081502e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Propoxur\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" C=CC#N\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=C1N(C2CCC(=O)NC2=O)C(=O)c3ccccc13\\n\",\n        \"output\": \" -2.676\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Monotropitoside\\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][O][C][Branch2][Ring1][C][C][O][C][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1ccncc1\\n\",\n        \"output\": \" 4-hydroxypyridine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CI\\n\",\n        \"output\": \" -1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Corticosterone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\\n\",\n        \"output\": \" o-Hydroxybenzamide\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H18/c1-4-5-6-7-8(2)3/h8H,4-7H2,1-3H3\\n\",\n        \"output\": \" -5.08\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][C][=Branch1][C][=O][O][C][C][Ring1][=Branch1][C][=Ring1][=C]\\n\",\n        \"output\": \" meconin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" Chlorthalidone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" OCCOc1ccccc1\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Bromooctane\\n\",\n        \"output\": \" InChI=1S/C8H17Br/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 3.3884415613920275e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Equilenin\\n\",\n        \"output\": \" InChI=1S/C18H18O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h2-5,10,16,19H,6-9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" 2.4547089156850306 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][Branch1][#C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][I][C][=C][C][=C][Ring1][S]\\n\",\n        \"output\": \" benodanil\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3\\n\",\n        \"output\": \" 0.001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][Branch1][Ring1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][=O]\\n\",\n        \"output\": \" -4.047\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Methylnaphthalene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CNC(=O)Oc1ccccc1C(C)C\\n\",\n        \"output\": \" Isoprocarb\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H\\n\",\n        \"output\": \" Napthalene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Malathion\\n\",\n        \"output\": \" CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Isoquinoline\\n\",\n        \"output\": \" InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Estragole\\n\",\n        \"output\": \" c1(OC)ccc(CC=C)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6Cl5NO2/c7-1-2(8)4(10)6(12(13)14)5(11)3(1)9\\n\",\n        \"output\": \" -5.82\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Diuron\\n\",\n        \"output\": \" 0.00015848931924611142 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Dimethylnaphthalene \\n\",\n        \"output\": \" Cc1ccc(C)c2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccc2c3c(ccc2c1)c4cccc5cccc3c45\\n\",\n        \"output\": \" Benzo(j)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H27OPS3/c1-4-7-10-15-14(13,16-11-8-5-2)17-12-9-6-3/h4-12H2,1-3H3\\n\",\n        \"output\": \" 7.244359600749906e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H28NO3PS2/c1-4-10-17-19(20,18-11-5-2)21-12-14(16)15-9-7-6-8-13(15)3/h13H,4-12H2,1-3H3\\n\",\n        \"output\": \" -4.15\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][/C][=C][/C]\\n\",\n        \"output\": \" trans-2-Pentene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCOCC\\n\",\n        \"output\": \" Ethyl propyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" m-Xylene \\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Tribromomethane\\n\",\n        \"output\": \" -1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Isonazid\\n\",\n        \"output\": \" c1nccc(C(=O)NN)c1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,2,4-Trimethylbenzene\\n\",\n        \"output\": \" Cc1ccc(C)c(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3\\n\",\n        \"output\": \" Caffeine\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methoprene\\n\",\n        \"output\": \" InChI=1S/C19H34O3/c1-15(2)22-18(20)14-17(4)11-8-10-16(3)12-9-13-19(5,6)21-7/h8,11,14-16H,9-10,12-13H2,1-7H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C]\\n\",\n        \"output\": \" Prometon\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Hexanone\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-3-5-6(7)4-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\",\n        \"output\": \" 1,4-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Oc1ccc(O)cc1\\n\",\n        \"output\": \" -0.17\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" t-Butylbenzene \\n\",\n        \"output\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H20/c1-8(2)6-7-9(3,4)5/h8H,6-7H2,1-5H3\\n\",\n        \"output\": \" -5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-8-16-15(7-1)17-9-3-5-13-11-12-14-6-4-10-18(16)20(14)19(13)17/h1-12H\\n\",\n        \"output\": \" -7.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H2Cl4/c3-1(4)2(5)6/h1-2H\\n\",\n        \"output\": \" 1,1,2,2-Tetrachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-7-17-15(4-1)12-16-9-8-13-5-3-6-14-10-11-18(17)20(16)19(13)14/h1-12H\\n\",\n        \"output\": \" Benzo(a)pyrene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCOC=O\\n\",\n        \"output\": \" 0.32359365692962827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Hydroxypyridine\\n\",\n        \"output\": \" 10.471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C(Cc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Bibenzyl \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H30OS/c1-18-8-7-14-12(13(18)5-6-17(18)20)4-3-11-9-15-16(21-15)10-19(11,14)2/h11-17,20H,3-10H2,1-2H3\\n\",\n        \"output\": \" 3.890451449942805e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" benzoin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC=C(C(=CC)c1ccc(O)cc1)c2ccc(O)cc2\\n\",\n        \"output\": \" -4.95\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Bromopropane\\n\",\n        \"output\": \" InChI=1S/C3H7Br/c1-2-3-4/h2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 1,4-Difluorobenzene\\n\",\n        \"output\": \" 0.010715193052376065 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Trichloroethylene\\n\",\n        \"output\": \" [Cl][C][=C][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-Nitroacetanilide\\n\",\n        \"output\": \" InChI=1S/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.691534803926914e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc2cc(O)c1C(=O)CC(Oc1c2)c3ccc(O)c(O)c3\\n\",\n        \"output\": \" Eriodictyol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H14/c1-3-5-7-6-4-2/h3,5H,4,6-7H2,1-2H3/b5-3+\\n\",\n        \"output\": \" trans-2-Heptene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2H2Cl4/c3-1-2(4,5)6/h1H2\\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" C=CC=O\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Nitrazepam\\n\",\n        \"output\": \" [O][=C][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][P][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1ccc2c(c1)c3ccccc3c4ccccc24\\n\",\n        \"output\": \" Triphenylene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" glucose\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 5,5-Dimethylbarbituric acid\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Chloropropane\\n\",\n        \"output\": \" InChI=1S/C3H7Cl/c1-2-3-4/h2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Azobenzene\\n\",\n        \"output\": \" [N][=Branch1][#Branch2][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Methylbutan-2-ol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Ethylnaphthalene\\n\",\n        \"output\": \" CCc1ccc2ccccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3\\n\",\n        \"output\": \" -2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" c1ccc2cc3cc4ccccc4cc3cc2c1\\n\",\n        \"output\": \" -8.6\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" -1.04\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-pyrrolidone\\n\",\n        \"output\": \" InChI=1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H6/c1-2/h1-2H3\\n\",\n        \"output\": \" Ethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][O]\\n\",\n        \"output\": \" 13.182567385564074 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" COC(=O)c1ccccc1OC2OC(COC3OCC(O)C(O)C3O)C(O)C(O)C2O\\n\",\n        \"output\": \" -0.742\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Isopropalin\\n\",\n        \"output\": \" InChI=1S/C15H23N3O4/c1-5-7-16(8-6-2)15-13(17(19)20)9-12(11(3)4)10-14(15)18(21)22/h9-11H,5-8H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.49\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Bromodichloromethane\\n\",\n        \"output\": \" BrC(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its solubility expressed as a logarithm in mol/L. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Nitropropane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Nitroethane\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Glyceryl triacetate\\n\",\n        \"output\": \" CC(=O)OCC(COC(=O)C)OC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Sorbitol\\n\",\n        \"output\": \" InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(O)c1ccccc1\\n\",\n        \"output\": \" 0.12022644346174127 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCOC(=O)c1ccccc1\\n\",\n        \"output\": \" 0.004786300923226385 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)Cl\\n\",\n        \"output\": \" 2-Chloropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)C)CC=C\\n\",\n        \"output\": \" 0.01958844673505989 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" OC3N=C(c1ccccc1Cl)c2cc(Cl)ccc2NC3=O\\n\",\n        \"output\": \" Lorazepam\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cyfluthrin\\n\",\n        \"output\": \" -7.337000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Atrazine\\n\",\n        \"output\": \" CCNc1nc(Cl)nc(NC(C)C)n1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Carbetamide\\n\",\n        \"output\": \" 0.014791083881682071 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)=CCC/C(C)=C\\\\CO\\n\",\n        \"output\": \" -2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H16N2O4/c1-11-5-3-6-12(9-11)18-16(20)22-14-8-4-7-13(10-14)17-15(19)21-2/h3-10H,1-2H3,(H,17,19)(H,18,20)\\n\",\n        \"output\": \" 1.5667510701081502e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3\\n\",\n        \"output\": \" Propylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN2C(=O)CN=C(c1ccccc1)c3cc(ccc23)N(=O)=O\\n\",\n        \"output\": \" Nimetazepam\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 2,3-Dimethylbutane\\n\",\n        \"output\": \" 0.000223872113856834 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N]\\n\",\n        \"output\": \" Ametryn\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Propane\\n\",\n        \"output\": \" InChI=1S/C3H8/c1-3-2/h3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Pentanol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-3-4-5(2)6/h5-6H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][S][C][S][=Branch1][C][=O][C][C][Branch1][Ring1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][NH1][C][=Branch1][C][=O][NH1][C][Ring1][Branch2][=O]\\n\",\n        \"output\": \" Sparsomycin (3,8mg/ml)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Propyne\\n\",\n        \"output\": \" [C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCC=O\\n\",\n        \"output\": \" Butyraldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCNC(=O)n1c(NC(=O)OC)nc2ccccc12\\n\",\n        \"output\": \" 1.309181922999407e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][N]\\n\",\n        \"output\": \" -2.084\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4N2O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H\\n\",\n        \"output\": \" -2.29\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H7Br/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\\n\",\n        \"output\": \" 0.00588843655355589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Fluometuron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1cccc(c1)C(F)(F)F\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H8ClNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\",\n        \"output\": \" -2.843\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)c1ccccc1\\n\",\n        \"output\": \" Bensulide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0020892961308540386 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H32O2/c1-14-12-17-18(21(3)9-6-16(25)13-20(14)21)7-11-23(5)19(17)8-10-22(23,4)15(2)24/h12-13,17-19H,6-11H2,1-5H3\\n\",\n        \"output\": \" Medrogestone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Urea\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H19NO2S/c1-14(2)13(15)17-11-7-6-10-16-12-8-4-3-5-9-12/h3-5,8-9H,6-7,10-11H2,1-2H3\\n\",\n        \"output\": \" Fenothiocarb\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCOCC\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H16N4O2S/c1-10(2,3)7-11-12-8(17-7)14-6(15)5-13(4)9(14)16/h6,15H,5H2,1-4H3\\n\",\n        \"output\": \" 0.013273944577297402 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][S]\\n\",\n        \"output\": \" 0.251188643150958 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" Lorazepam\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-14-8-4-2-6-12(14)10-13-7-3-5-9-15(11)13/h2-10H,1H3\\n\",\n        \"output\": \" 1.288249551693135e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCI\\n\",\n        \"output\": \" Iodoethane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3-8H,1-2H3\\n\",\n        \"output\": \" 0.0007413102413009177 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Pentene \\n\",\n        \"output\": \" [C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccccc1O\\n\",\n        \"output\": \" 2-Methylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-7-10(2)12-6-4-3-5-11(12)8-9/h3-8H,1-2H3\\n\",\n        \"output\": \" -4.29\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\\n\",\n        \"output\": \" 0.01513561248436208 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" ClC(=C(Cl)Cl)Cl\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H10O3/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3\\n\",\n        \"output\": \" Ethyl-p-hydroxybenzoate \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCOC(=O)C\\n\",\n        \"output\": \" Propyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCSCCSP(=S)(OC)OC\\n\",\n        \"output\": \" -3.091\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" m-Xylene \\n\",\n        \"output\": \" Cc1cccc(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Ring1][=C]\\n\",\n        \"output\": \" Chloroxuron\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC1(C)C(C=C(Br)Br)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" 3.962780342554385e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Secobarbital\\n\",\n        \"output\": \" InChI=1S/C12H18N2O3/c1-4-6-8(3)12(7-5-2)9(15)13-11(17)14-10(12)16/h5,8H,2,4,6-7H2,1,3H3,(H2,13,14,15,16,17)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Methyl-2-hexanol\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 1-Methylphenanthrene\\n\",\n        \"output\": \" 1.4125375446227554e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Cyclopentyl-5-spirobarbituric acid\\n\",\n        \"output\": \" InChI=1S/C8H10N2O3/c11-5-8(3-1-2-4-8)6(12)10-7(13)9-5/h1-4H2,(H2,9,10,11,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H20O2/c1-3-4-5-6-7-8-9-10(11)12-2/h3-9H2,1-2H3\\n\",\n        \"output\": \" Methyl nonanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1c(NC(=O)c2ccccc2(I))cccc1\\n\",\n        \"output\": \" -4.21\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Dibenzothiophene\\n\",\n        \"output\": \" 4.168693834703355e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H16/c1-7-5-3-4-6-8(7)2/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" cis-1,2-Dimethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" hydrobenzoin\\n\",\n        \"output\": \" InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Butanol\\n\",\n        \"output\": \" CCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H19N5S/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,2-Dimethylbutane\\n\",\n        \"output\": \" InChI=1S/C6H14/c1-5-6(2,3)4/h5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][C][=C][C][C][Ring1][Branch1][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl]\\n\",\n        \"output\": \" -6.317\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Phenytoin\\n\",\n        \"output\": \" InChI=1S/C15H12N2O2/c18-13-15(17-14(19)16-13,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H2,16,17,18,19)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=O]\\n\",\n        \"output\": \" 2.0892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Chlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3\\n\",\n        \"output\": \" -3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Chlorbromuron\\n\",\n        \"output\": \" 0.0001191242008027375 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2H2ClN/c3-1-2-4/h1H2\\n\",\n        \"output\": \" -0.092\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)\\n\",\n        \"output\": \" Benzamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=S][NH1][Ring1][Branch2]\\n\",\n        \"output\": \" methylthiouracil\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Siduron\\n\",\n        \"output\": \" 7.762471166286911e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccc2ccccc2c1\\n\",\n        \"output\": \" 2-Napthol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 0.001202264434617413 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-5(2)4-8-6(3)7/h5H,4H2,1-3H3\\n\",\n        \"output\": \" 0.06165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Aldrin\\n\",\n        \"output\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch1][C][=C][Ring1][Branch1][C][Ring1][#Branch1][C][Ring1][=N][Branch1][C][Cl][C][Ring1][N][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cccc2ccccc12\\n\",\n        \"output\": \" 1-Chloronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,5-Dimethlnapthalene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCCCCC(=O)C\\n\",\n        \"output\": \" -2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" m-Fluorobromobenzene\\n\",\n        \"output\": \" 0.0021379620895022326 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Carbromal\\n\",\n        \"output\": \" [C][C][C][Branch1][C][Br][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][Branch1][C][N][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C11H19N3O/c1-4-6-7-9-8(3)13-11(12-5-2)14-10(9)15/h4-7H2,1-3H3,(H2,12,13,14,15)\\n\",\n        \"output\": \" 0.0009375620069258802 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3\\n\",\n        \"output\": \" 2-Methylbutane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Br2/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" 1,2-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,2-Dimethylpropanol\\n\",\n        \"output\": \" CC(C)(C)CO\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3\\n\",\n        \"output\": \" p-Methylaniline \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Niclosamide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Napthalene\\n\",\n        \"output\": \" c1ccc2ccccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H6N4/c1-5-6-7(11-4-10-5)9-3-2-8-6/h2-4H,1H3\\n\",\n        \"output\": \" 4-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3,5-Dichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H4Cl2O/c7-4-1-5(8)3-6(9)2-4/h1-3,9H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Methylbutan-2-ol\\n\",\n        \"output\": \" CCC(C)(C)O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][I][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" -6.62\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5,5-Diisopropylbarbital\\n\",\n        \"output\": \" InChI=1S/C10H16N2O3/c1-5(2)10(6(3)4)7(13)11-9(15)12-8(10)14/h5-6H,1-4H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4-Chlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 2-Isopropyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethion\\n\",\n        \"output\": \" InChI=1S/C9H22O4P2S4/c1-5-10-14(16,11-6-2)18-9-19-15(17,12-7-3)13-8-4/h5-9H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][=C][Branch1][C][C][N][=C][Branch1][Ring2][N][C][C][NH1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 0.0009375620069258802 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)(C)c1ccccc1\\n\",\n        \"output\": \" t-Butylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H9Br/c1-4(2)3-5/h4H,3H2,1-2H3\\n\",\n        \"output\": \" 1-Bromo-2-methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CC(C)c1ccc(C)cc1\\n\",\n        \"output\": \" 0.00016982436524617443 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Caffeine\\n\",\n        \"output\": \" InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C3H6O/c1-2-3-4/h3H,2H2,1H3\\n\",\n        \"output\": \" 3.8018939632056115 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methyl octanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,3,5-Trichlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Pebulate\\n\",\n        \"output\": \" 0.0002951209226666387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Dialifos\\n\",\n        \"output\": \" 4.5708818961487516e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Chloronitrobenzene\\n\",\n        \"output\": \" Clc1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 6-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethyl nonanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)\\n\",\n        \"output\": \" Succinimide\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C]\\n\",\n        \"output\": \" 0.12589254117941673 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Iodoethane\\n\",\n        \"output\": \" [C][C][I]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" o-Nitroaniline\\n\",\n        \"output\": \" Nc1ccccc1N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-7-14-13(6-1)12-19-16-9-4-3-8-15(16)18-11-5-10-17(14)20(18)19/h1-12H\\n\",\n        \"output\": \" Benzo(b)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H12F3NO4S2/c1-10-9-12(23(19,20)11-5-3-2-4-6-11)7-8-13(10)18-24(21,22)14(15,16)17/h2-9,18H,1H3\\n\",\n        \"output\": \" Perfluidone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" salicylanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" salicylanilide\\n\",\n        \"output\": \" InChI=1S/C13H11NO2/c15-12-9-5-4-8-11(12)13(16)14-10-6-2-1-3-7-10/h1-9,15H,(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" Methyl propyl ether \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\\n\",\n        \"output\": \" 4.5708818961487516e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14S/c1-5(2)7-6(3)4/h5-6H,1-4H3\\n\",\n        \"output\": \" Diisopropylsulfide\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H16N2O3/c1-5(2)10(6(3)4)7(13)11-9(15)12-8(10)14/h5-6H,1-4H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" -2.766\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4BrCl/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" 0.0006165950018614823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" -6.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" COC(=O)c1ccccc1\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Propionaldehyde\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][O][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 0.15135612484362082 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Isopropyltoluene\\n\",\n        \"output\": \" CC(C)c1ccccc1C\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Nitropropane\\n\",\n        \"output\": \" InChI=1S/C3H7NO2/c1-3(2)4(5)6/h3H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc(cc1N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" 2,4-Dinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Isoquinoline\\n\",\n        \"output\": \" c1ccc2cnccc2c1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc2ccccc2c1\\n\",\n        \"output\": \" -3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1SC(=S)NC1(=O)\\n\",\n        \"output\": \" rhodanine\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Bromodichloromethane\\n\",\n        \"output\": \" 0.028840315031266057 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][O]\\n\",\n        \"output\": \" Thymol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Pyridazine\\n\",\n        \"output\": \" c1ccnnc1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [N][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.07\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Chlorobutane\\n\",\n        \"output\": \" CCCCCl\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][Branch1][C][C][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.00022908676527677723 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Diisopropyl ether \\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-5(2)7-6(3)4/h5-6H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dibenzothiophene\\n\",\n        \"output\": \" c1ccc2c(c1)sc3ccccc23\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CNN\\n\",\n        \"output\": \" Methyl hydrazine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][=C][Branch1][S][C][=C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" Equilenin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Heptanol\\n\",\n        \"output\": \" -1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][N][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=O][N][=C][Ring1][Branch2][N][Branch1][S][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O][C][=Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][=Branch2][C]\\n\",\n        \"output\": \" Riboflavin\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O2/c1-3-7-5-6-8-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" -0.77\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" o-Methoxyphenol\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCC\\n\",\n        \"output\": \" -3.18\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14O2/c1-4-7-6(3)8-5-2/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" 1,1-Diethoxyethane \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C18H32O16/c19-1-5-8(22)11(25)13(27)16(31-5)30-3-7-9(23)12(26)14(28)17(32-7)34-18(4-21)15(29)10(24)6(2-20)33-18/h5-17,19-29H,1-4H2\\n\",\n        \"output\": \" Raffinose\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Etomidate\\n\",\n        \"output\": \" 1.8407720014689545e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" m-Methylaniline\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2-Dibromobenzene\\n\",\n        \"output\": \" [Br][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1(Br)c(Br)cc(Br)cc1\\n\",\n        \"output\": \" 1,2,4-tribromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(Cl)(Cl)Cl\\n\",\n        \"output\": \" 1,1,1-Trichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 4-Methyl-2-pentanone\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-5(2)4-6(3)7/h5H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H2Cl8/c13-5-1-3(7(15)11(19)9(5)17)4-2-6(14)10(18)12(20)8(4)16/h1-2H\\n\",\n        \"output\": \" 2,2',3,3',4,4',5,5'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" 0.007943282347242814 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" Decalin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2H6S2/c1-3-4-2/h1-2H3\\n\",\n        \"output\": \" -1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H18N2O3/c1-4-6-8(3)12(7-5-2)9(15)13-11(17)14-10(12)16/h5,8H,2,4,6-7H2,1,3H3,(H2,13,14,15,16,17)\\n\",\n        \"output\": \" Secobarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][S][C][C]\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Bibenzyl \\n\",\n        \"output\": \" -4.62\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Hexachloro-1,3-butadiene\\n\",\n        \"output\": \" 1.2022644346174132e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][S][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Butylate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Dichlorobenzene\\n\",\n        \"output\": \" Clc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)CBr\\n\",\n        \"output\": \" 1-Bromo-2-methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" Chlorazine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p,p'-Biphenyldiamine \\n\",\n        \"output\": \" Nc1ccc(cc1)c2ccc(N)cc2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-5(2,3)6-4/h1-4H3\\n\",\n        \"output\": \" 0.5754399373371569 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1cncc(C)c1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chloroethylene\\n\",\n        \"output\": \" InChI=1S/C2H3Cl/c1-2-3/h2H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dibromomethane\\n\",\n        \"output\": \" InChI=1S/CH2Br2/c2-1-3/h1H2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Bromotoluene\\n\",\n        \"output\": \" Cc1ccccc1Br\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Bromomethane\\n\",\n        \"output\": \" [C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Isopentyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-Chlorotoluene\\n\",\n        \"output\": \" InChI=1S/C7H7Cl/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCC(C)O\\n\",\n        \"output\": \" 2-Undecanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2,3-Dimethylpyridine\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][O]\\n\",\n        \"output\": \" 0.251188643150958 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Dinitrobenzene\\n\",\n        \"output\": \" O=N(=O)c1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3\\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Nitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Octanone\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H12ClNO2/c1-7(2)14-10(13)12-9-5-3-4-8(11)6-9/h3-7H,1-2H3,(H,12,13)\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCNC(=S)NCC\\n\",\n        \"output\": \" 0.034673685045253165 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Acridine\\n\",\n        \"output\": \" [C][=C][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C3H7NO2/c1-3(2)4(5)6/h3H,1-2H3\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,3,4-Trichlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Kepone\\n\",\n        \"output\": \" [Cl][C][Branch1][P][C][=Branch1][C][=O][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][Branch2][Cl][C][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring1][N][Ring1][#Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Theophylline\\n\",\n        \"output\": \" -1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -3.18\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Sorbitol\\n\",\n        \"output\": \" 12.302687708123818 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-3-4-5(6)7-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Cyclohexanol \\n\",\n        \"output\": \" InChI=1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H16ClN5/c1-4-11-8-12-7(10)13-9(14-8)15(5-2)6-3/h4-6H2,1-3H3,(H,11,12,13,14)\\n\",\n        \"output\": \" 8.709635899560814e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Hexane \\n\",\n        \"output\": \" InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" 0.00010964781961431851 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H20N2S4/c1-5-11(6-2)9(13)15-16-10(14)12(7-3)8-4/h5-8H2,1-4H3\\n\",\n        \"output\": \" Disulfiram\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Octanol\\n\",\n        \"output\": \" CCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Parathion\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 2-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Endrin\\n\",\n        \"output\": \" InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Trichloronate\\n\",\n        \"output\": \" InChI=1S/C10H12Cl3O2PS/c1-3-14-16(17,4-2)15-10-6-8(12)7(11)5-9(10)13/h5-6H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cccc(N)c1\\n\",\n        \"output\": \" m-Methylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dibromomethane\\n\",\n        \"output\": \" [Br][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H4/c1-2/h1-2H2\\n\",\n        \"output\": \" Ethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10Cl10/c11-1-2(12)6(16)9(19,5(1)15)10(20)7(17)3(13)4(14)8(10)18\\n\",\n        \"output\": \" -7.278\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=N][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Pyridazine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3\\n\",\n        \"output\": \" Hydrocortisone \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diphenyl ether \\n\",\n        \"output\": \" [O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H15I/c1-2-3-4-5-6-7-8/h2-7H2,1H3\\n\",\n        \"output\": \" 1.5488166189124828e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Propane\\n\",\n        \"output\": \" CCC\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" t-Crotonaldehyde\\n\",\n        \"output\": \" InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3/b3-2+\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H\\n\",\n        \"output\": \" 2.511886431509582e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1-Octyne \\n\",\n        \"output\": \" -3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,5-Hexadiene \\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H6ClN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2\\n\",\n        \"output\": \" p-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Nc1ccccc1N(=O)=O\\n\",\n        \"output\": \" o-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12)\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 1-Bromohexane\\n\",\n        \"output\": \" 0.0001548816618912481 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(=O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C\\n\",\n        \"output\": \" 3.8018939632056124e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H16O/c1-9(2)5-4-6-10(3)7-8-11/h5,7-8H,4,6H2,1-3H3\\n\",\n        \"output\": \" 0.008709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H17Cl2NOS/c1-7(2)13(8(3)4)10(14)15-6-9(12)5-11/h5,7-8H,6H2,1-4H3\\n\",\n        \"output\": \" Diallate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccccc1\\n\",\n        \"output\": \" Benzene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1cc2ccc3cccc4ccc(c1)c2c34\\n\",\n        \"output\": \" Pyrene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][C][=O]\\n\",\n        \"output\": \" Isobutyl formate\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chloropham\\n\",\n        \"output\": \" InChI=1S/C10H12ClNO2/c1-7(2)14-10(13)12-9-5-3-4-8(11)6-9/h3-7H,1-2H3,(H,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)\\n\",\n        \"output\": \" O-Ethyl carbamate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3\\n\",\n        \"output\": \" -4.14\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Hydroxyprogesterone-17a\\n\",\n        \"output\": \" 0.00015240527537972924 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2-Diethylbenzene\\n\",\n        \"output\": \" CCc1ccccc1CC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Thiophene\\n\",\n        \"output\": \" c1ccsc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-methoxypteridine\\n\",\n        \"output\": \" [C][O][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3\\n\",\n        \"output\": \" -3.77\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OCC1OC(CO)(OC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)C(O)C1O\\n\",\n        \"output\": \" Raffinose\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" ethyl cinnamate\\n\",\n        \"output\": \" CCOC(=O)C=Cc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][Ring1][O][=Ring1][#Branch1]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)C=C\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Dodecanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H6N4O/c1-12-6-3-9-7-5(11-6)2-8-4-10-7/h2-4H,1H3\\n\",\n        \"output\": \" 6-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][F]\\n\",\n        \"output\": \" Flutriafol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Diosgenin\\n\",\n        \"output\": \" 4.78630092322638e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" N,N-Diethylaniline\\n\",\n        \"output\": \" -3.03\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Octanol\\n\",\n        \"output\": \" InChI=1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Chloroethylene\\n\",\n        \"output\": \" [Cl][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Trichloronate\\n\",\n        \"output\": \" CCOP(=S)(CC)Oc1cc(Cl)c(Cl)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H18O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h3-12,19-20H,1-2H3\\n\",\n        \"output\": \" Dienestrol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][#N]\\n\",\n        \"output\": \" 0.004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC23Cc1cnoc1C=C2CCC4C3CCC5(C)C4CCC5(O)C#C\\n\",\n        \"output\": \" Danazol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc2c(c1)sc3ccccc23\\n\",\n        \"output\": \" Dibenzothiophene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C\\n\",\n        \"output\": \" -3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 4.3651583224016566e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Methyl acrylate\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" ClC4=C(Cl)C5(Cl)C3C1CC(C2OC12)C3C4(Cl)C5(Cl)Cl\\n\",\n        \"output\": \" 5.128613839913648e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Buthidazole\\n\",\n        \"output\": \" CN1CC(O)N(C1=O)c2nnc(s2)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCCCC#C\\n\",\n        \"output\": \" 0.004365158322401661 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)C(C)C\\n\",\n        \"output\": \" 0.000223872113856834 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Coronene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][C][C][Ring1][S][=C][Ring1][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C\\n\",\n        \"output\": \" Hydroxyprogesterone-17a\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H34O4/c1-3-5-15-21-17(19)13-11-9-7-8-10-12-14-18(20)22-16-6-4-2/h3-16H2,1-2H3\\n\",\n        \"output\": \" dibutyl sebacate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1ccccc1(OC(=O)NC)\\n\",\n        \"output\": \" 0.01573982864466219 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 5-Ethyl-5-(3-methylbutyl)barbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClCC(Cl)(Cl)Cl\\n\",\n        \"output\": \" 1,1,1,2-Tetrachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Propanoyloxymethylphenytoin\\n\",\n        \"output\": \" -4.907\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,3-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" o-Nitrotoluene\\n\",\n        \"output\": \" Cc1ccccc1N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Equilin\\n\",\n        \"output\": \" CC34CCC1C(=CCc2cc(O)ccc12)C3CCC4=O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Fc1ccccc1Br\\n\",\n        \"output\": \" 0.001995262314968879 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][C][=C][N][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 2-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(=O)CC(c1ccc(Cl)cc1)c2c(O)c3ccccc3oc2=O\\n\",\n        \"output\": \" Coumachlor\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Biphenyl\\n\",\n        \"output\": \" -4.345\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch1][Ring1][S][C][C][Branch1][C][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" -4.57\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" phthalamide\\n\",\n        \"output\": \" InChI=1S/C8H7NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-6H,(H,9,10,11)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOc1ccccc1\\n\",\n        \"output\": \" Phenetole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Triclosan\\n\",\n        \"output\": \" Oc1cc(Cl)ccc1Oc2ccc(Cl)cc2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Diphenylamine\\n\",\n        \"output\": \" InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" Pteridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cl\\\\C=C/Cl\\n\",\n        \"output\": \" cis 1,2-Dichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-2-3-7-10-8-5-4-6-9-10/h4-6,8-9H,2-3,7H2,1H3\\n\",\n        \"output\": \" Butylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" -8.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CNC(=O)Oc1cccc2CC(C)(C)Oc12\\n\",\n        \"output\": \" 0.001584893192461114 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1c2ccccc2C(=O)c3ccccc13\\n\",\n        \"output\": \" Anthraquinone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3\\n\",\n        \"output\": \" Ethofumesate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dioxacarb\\n\",\n        \"output\": \" InChI=1S/C11H13NO4/c1-12-11(13)16-9-5-3-2-4-8(9)10-14-6-7-15-10/h2-5,10H,6-7H2,1H3,(H,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" cis-2-Pentene\\n\",\n        \"output\": \" InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3-\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Terbumeton\\n\",\n        \"output\": \" [C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H22O2/c1-3-4-5-6-7-8-9-10-11(12)13-2/h3-10H2,1-2H3\\n\",\n        \"output\": \" Methyl decanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Chloropicrin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" norflurazon\\n\",\n        \"output\": \" InChI=1S/C12H9ClF3N3O/c1-17-9-6-18-19(11(20)10(9)13)8-4-2-3-7(5-8)12(14,15)16/h2-6,17H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][N][=C][Branch1][Ring1][S][C][C][=Branch1][C][=O][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.106\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(=O)OC\\n\",\n        \"output\": \" Methyl propionate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3\\n\",\n        \"output\": \" -2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" OCC1OC(C(O)C1O)n2cnc3c(O)ncnc23\\n\",\n        \"output\": \" 0.0588843655355589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2',3,3',4,4',5,5'-PCB\\n\",\n        \"output\": \" Clc1cc(c(Cl)c(Cl)c1Cl)c2cc(Cl)c(Cl)c(Cl)c2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Pentyl acetate\\n\",\n        \"output\": \" -1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Permethrin\\n\",\n        \"output\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OCc2cccc(Oc3ccccc3)c2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\\n\",\n        \"output\": \" 0.0024210290467361778 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Nonanol\\n\",\n        \"output\": \" InChI=1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Talbutal\\n\",\n        \"output\": \" CCC(C)C1(CC=C)C(=O)NC(=O)NC1=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" p-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCBr\\n\",\n        \"output\": \" 1-Bromobutane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][/C][C][C][C][Branch1][C][\\\\C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.3884415613920276e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C18H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h19H,2-18H2,1H3\\n\",\n        \"output\": \" 3.981071705534969e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" NC(=S)N\\n\",\n        \"output\": \" 2.0892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCO\\n\",\n        \"output\": \" 1-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][S][C][C][S][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C]\\n\",\n        \"output\": \" -3.091\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" citral\\n\",\n        \"output\": \" InChI=1S/C10H16O/c1-9(2)5-4-6-10(3)7-8-11/h5,7-8H,4,6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][=C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" 7.585775750291836e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H4O/c1-2-3-4/h2-3H,1H2\\n\",\n        \"output\": \" Acrolein\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1(O)cc(O)ccc1CCCCCC\\n\",\n        \"output\": \" 4-hexylresorcinol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CNC(=O)ON=C(SC)C(=O)N(C)C\\n\",\n        \"output\": \" Oxamyl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)c1ccccc1\\n\",\n        \"output\": \" 5-Ethyl-5-phenylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCc1ccccn1\\n\",\n        \"output\": \" 3.2359365692962827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][S]\\n\",\n        \"output\": \" Ethanethiol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)C(C)O\\n\",\n        \"output\": \" 0.660693448007596 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propyl butyrate\\n\",\n        \"output\": \" CCCC(=O)OC\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCOP(=O)(OCC)OCC\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Nc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" -2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H5Cl5/c13-6-4-9(16)12(10(17)5-6)11-7(14)2-1-3-8(11)15/h1-5H\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3/c7-4-1-5(8)3-6(9)2-4/h1-3H\\n\",\n        \"output\": \" 1,3,5-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H4O/c1-2-4-5-3-1/h1-4H\\n\",\n        \"output\": \" Furane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Isoprocarb\\n\",\n        \"output\": \" InChI=1S/C11H15NO2/c1-8(2)9-6-4-5-7-10(9)14-11(13)12-3/h4-8H,1-3H3,(H,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" d-Limonene\\n\",\n        \"output\": \" -4.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its oil solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Piperine\\n\",\n        \"output\": \" InChI=1S/C17H19NO3/c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15/h2-3,6-9,12H,1,4-5,10-11,13H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" difluron\\n\",\n        \"output\": \" Fc1cccc(F)c1C(=O)NC(=O)Nc2ccc(Cl)cc2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][C][C][=N][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Ring1][=N][Cl]\\n\",\n        \"output\": \" Pyrazon\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CNC(=O)Oc1cccc(N=CN(C)C)c1\\n\",\n        \"output\": \" -2.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H11N/c1-2-9-8-6-4-3-5-7-8/h3-7,9H,2H2,1H3\\n\",\n        \"output\": \" 0.0199526231496888 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Bromopentane\\n\",\n        \"output\": \" CCCCCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][/C][=C][/C][=O]\\n\",\n        \"output\": \" t-Crotonaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Endrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCC(C)(C)O\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" XMC\\n\",\n        \"output\": \" InChI=1S/C10H13NO2/c1-7-4-8(2)6-9(5-7)13-10(12)11-3/h4-6H,1-3H3,(H,11,12)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)CCO\\n\",\n        \"output\": \" 3-Methylbutan-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Bromochloromethane\\n\",\n        \"output\": \" InChI=1S/CH2BrCl/c2-1-3/h1H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Heptanoyloxymethylphenytoin\\n\",\n        \"output\": \" [O][=C][N][Branch1][=N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Propyl propanoate\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H12/c1-11-7-9-13(10-8-11)12-5-3-2-4-6-12/h2-10H,1H3\\n\",\n        \"output\": \" 4-Methylbiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][N][Cl]\\n\",\n        \"output\": \" Quintozene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" O=C3CN=C(c1ccccc1)c2cc(ccc2N3)N(=O)=O\\n\",\n        \"output\": \" 0.0001599558028614668 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-6(2)7(3,4)5/h6H,1-5H3\\n\",\n        \"output\": \" 2,2,3-Trimethylbutane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Cyclohexane\\n\",\n        \"output\": \" InChI=1S/C6H12/c1-2-4-6-5-3-1/h1-6H2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [I][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.000977237220955811 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,2-Benzenediol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ethyl propionate\\n\",\n        \"output\": \" InChI=1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-5-6-8(4-2)7-9/h8-9H,3-7H2,1-2H3\\n\",\n        \"output\": \" -2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" -4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,1,2-Trichloroethane\\n\",\n        \"output\": \" [Cl][C][C][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.7585775750291838 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Methylaniline \\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)\\n\",\n        \"output\": \" Rovral\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Ethylcyclohexane\\n\",\n        \"output\": \" -4.25\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 5-Allyl-5-ethylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)CC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCC(=O)C\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCCCCCCCCCCCO\\n\",\n        \"output\": \" -5.84\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COC=O\\n\",\n        \"output\": \" 3.8018939632056115 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Chloroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc(Cl)cc1\\n\",\n        \"output\": \" 4-Chlorotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Anthraquinone\\n\",\n        \"output\": \" -5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" N-Methylaniline \\n\",\n        \"output\": \" -1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-Heptanol\\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-3-5-7(8)6-4-2/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C=CCC=C\\n\",\n        \"output\": \" 1,4-Pentadiene \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methy-2-Butene\\n\",\n        \"output\": \" InChI=1S/C5H10/c1-4-5(2)3/h4H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Formetanate\\n\",\n        \"output\": \" 0.004570881896148752 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Heptene\\n\",\n        \"output\": \" InChI=1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 6-methoxypteridine\\n\",\n        \"output\": \" COc2cnc1ncncc1n2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Acetonitrile\\n\",\n        \"output\": \" 1.8197008586099834 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Napthol\\n\",\n        \"output\": \" 0.005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Decanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 2-Methyl-1,3-Butadiene \\n\",\n        \"output\": \" 0.009332543007969915 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Pyridine\\n\",\n        \"output\": \" [C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" -1.98\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Carbazole\\n\",\n        \"output\": \" -5.27\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-2-3-4-7-5-6/h5H,2-4H2,1H3\\n\",\n        \"output\": \" -1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H6Cl8/c11-3-1-2-4(5(3)12)9(16)7(14)6(13)8(2,15)10(9,17)18/h2-5H,1H2\\n\",\n        \"output\": \" Chlordane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" -4.29\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Acetanilide\\n\",\n        \"output\": \" InChI=1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CC1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C\\n\",\n        \"output\": \" 0.00010023052380779004 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][=C][C][C][/C][Branch1][C][C][=C][\\\\C][O]\\n\",\n        \"output\": \" 0.0034673685045253167 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methyl octanoate\\n\",\n        \"output\": \" InChI=1S/C9H18O2/c1-3-4-5-6-7-8-9(10)11-2/h3-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 5-Allyl-5-phenylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][N][C][Branch1][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Isofenphos\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCNc1nc(NC(C)C)nc(SC)n1\\n\",\n        \"output\": \" Ametryn\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)c1ccc(C)cc1O\\n\",\n        \"output\": \" -2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOC=O\\n\",\n        \"output\": \" Ethyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C=C\\n\",\n        \"output\": \" Ethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H8N2/c1-3-9-5-6-11-10(4-2-7-13-11)12(9)14-8-1/h1-8H\\n\",\n        \"output\": \" 0.0020892961308540386 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Atovaquone(0,430mg/ml) - neutral\\n\",\n        \"output\": \" [O][C][=C][Branch2][Ring1][=Branch1][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3\\n\",\n        \"output\": \" Butan-2-ol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Chloroanisole\\n\",\n        \"output\": \" COc1ccccc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.006053408747539136 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Anilofos\\n\",\n        \"output\": \" InChI=1S/C13H19ClNO3PS2/c1-10(2)15(12-7-5-11(14)6-8-12)13(16)9-21-19(20,17-3)18-4/h5-8,10H,9H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0003133285724315589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H12ClN3O3S/c1-2-9-13-7-4-6(11)8(18(12,16)17)3-5(7)10(15)14-9/h3-4,9,13H,2H2,1H3,(H,14,15)(H2,12,16,17)\\n\",\n        \"output\": \" Quinethazone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Chloroxuron\\n\",\n        \"output\": \" CN(C)C(=O)Nc2ccc(Oc1ccc(Cl)cc1)cc2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethyl propyl ether\\n\",\n        \"output\": \" [C][C][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3-Chlorobiphenyl\\n\",\n        \"output\": \" InChI=1S/C12H9Cl/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H18N2O3/c1-7(2)5-6-12(8(3)4)9(15)13-11(17)14-10(12)16/h5,8H,6H2,1-4H3,(H2,13,14,15,16,17)\\n\",\n        \"output\": \" 0.002552701302661247 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H\\n\",\n        \"output\": \" 6.456542290346549e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][C]\\n\",\n        \"output\": \" 7.762471166286911e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)c1ccccc1C\\n\",\n        \"output\": \" 2-Isopropyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H14NO5P/c1-6(5-7(9)8-2)13-14(10,11-3)12-4/h5H,1-4H3,(H,8,9)\\n\",\n        \"output\": \" Azodrin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,2',3,4,5,5',6-PCB\\n\",\n        \"output\": \" InChI=1S/C12H3Cl7/c13-4-1-2-6(14)5(3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Fenpropathrin\\n\",\n        \"output\": \" InChI=1S/C22H23NO3/c1-21(2)19(22(21,3)4)20(24)26-18(14-23)15-9-8-12-17(13-15)25-16-10-6-5-7-11-16/h5-13,18-19H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1OC(O)C(O)C(O)C1O\\n\",\n        \"output\": \" L-arabinose\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H10N2O3/c11-5-8(3-1-2-4-8)6(12)10-7(13)9-5/h1-4H2,(H2,9,10,11,12,13)\\n\",\n        \"output\": \" 0.004477133041763623 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H13NO2/c1-7-4-8(2)6-9(5-7)13-10(12)11-3/h4-6H,1-3H3,(H,11,12)\\n\",\n        \"output\": \" -2.5810000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" OCC(O)COC(=O)c1ccccc1Nc2ccnc3cc(Cl)ccc23\\n\",\n        \"output\": \" 2.6853444456585036e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2H5I/c1-2-3/h2H2,1H3\\n\",\n        \"output\": \" 0.025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-7-4-5-8(2)9(3)6-7/h4-6H,1-3H3\\n\",\n        \"output\": \" 1,2,4-Trimethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" L-arabinose\\n\",\n        \"output\": \" InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H13NO4S/c1-9-11(18(15,16)8-7-17-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\\n\",\n        \"output\": \" Oxycarboxin\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1cc(C)c2ccccc2c1\\n\",\n        \"output\": \" -4.29\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" m-Nitrotoluene\\n\",\n        \"output\": \" InChI=1S/C7H7NO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][S][S][C][C]\\n\",\n        \"output\": \" 0.0038018939632056127 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-4-8-7(2)5-6/h3-5H,1-2H3\\n\",\n        \"output\": \" 2,4-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Nitrapyrin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Fluorene \\n\",\n        \"output\": \" InChI=1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" 1.0964781961431851e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,5-Hexadiene \\n\",\n        \"output\": \" C=CCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O]\\n\",\n        \"output\": \" 0.5701642722807475 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3\\n\",\n        \"output\": \" 0.008709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC34CCC1C(CCC2=CC(=O)CCC12C)C3CCC4=O\\n\",\n        \"output\": \" -3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H20O/c1-3-4-5-6-7-8-9-10(2)11/h3-9H2,1-2H3\\n\",\n        \"output\": \" 2-Decanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Carbanilide\\n\",\n        \"output\": \" 0.000707945784384138 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2Cl4/c3-1(4)2(5)6\\n\",\n        \"output\": \" -2.54\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=Branch1][C][=O][N][Ring1][O]\\n\",\n        \"output\": \" -1.655\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" -3.364\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" t-Crotonaldehyde\\n\",\n        \"output\": \" [C][/C][=C][/C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H10/c1-7-3-5-8(2)6-4-7/h3-6H,1-2H3\\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][=N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" 2-Methylphenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3,4-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Nitroanisole\\n\",\n        \"output\": \" COc1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methylcyclohexane \\n\",\n        \"output\": \" CC1CCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" o-Xylene \\n\",\n        \"output\": \" 0.001584893192461114 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-4-5-6-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" Methyl butyl ether \\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,6-Dimethylnaphthalene \\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][Ring1][#Branch1][=C][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1(=O)NC(=O)NC(=O)C1(O)C2(O)C(=O)NC(=O)NC2(=O)\\n\",\n        \"output\": \" alloxantin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Tetrahydropyran \\n\",\n        \"output\": \" C1CCOCC1\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" chloropropylate\\n\",\n        \"output\": \" InChI=1S/C17H16Cl2O3/c1-11(2)22-16(20)17(21,12-6-8-14(18)9-7-12)13-4-3-5-15(19)10-13/h3-11,21H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" COc1ccccc1\\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][C][O][C][C]\\n\",\n        \"output\": \" -0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCOC\\n\",\n        \"output\": \" Methyl propyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H8FNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\",\n        \"output\": \" -1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 5-Allyl-5-phenylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring2][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H14N2O2/c1-2-12(9-6-4-3-5-7-9)10(15)13-8-14-11(12)16/h3-7H,2,8H2,1H3,(H,13,15)(H,14,16)\\n\",\n        \"output\": \" Primidone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Iodoethane\\n\",\n        \"output\": \" CCI\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(N(=O)=O)c(C)c1\\n\",\n        \"output\": \" 9.120108393559096e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H4ClI/c7-5-1-3-6(8)4-2-5/h1-4H\\n\",\n        \"output\": \" p-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][C][#N]\\n\",\n        \"output\": \" 0.8090958991783823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2-Ethyl-1-hexanol\\n\",\n        \"output\": \" -2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Equilin\\n\",\n        \"output\": \" -5.282\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Monotropitoside\\n\",\n        \"output\": \" -0.742\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" parallelogram\\n\",\n        \"output\": \" parallelogram does not have compound\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][N][=C][Branch1][C][Cl][N][Branch1][Ring2][N][=Ring1][=Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Isazofos\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C]\\n\",\n        \"output\": \" 0.013489628825916533 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Dicapthon\\n\",\n        \"output\": \" -4.31\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)(C)Cc1ccccc1\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Tribromomethane\\n\",\n        \"output\": \" BrC(Br)Br\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(C)CC\\n\",\n        \"output\": \" 3-Methylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Triallate\\n\",\n        \"output\": \" CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benzo(b)fluorene\\n\",\n        \"output\": \" InChI=1S/C17H12/c1-2-6-13-11-17-15(9-12(13)5-1)10-14-7-3-4-8-16(14)17/h1-9,11H,10H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Phenytoin\\n\",\n        \"output\": \" 7.998342550070293e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 1,4-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][N][Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][Ring1][=C][=O]\\n\",\n        \"output\": \" -2.338\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][=Branch1][Ring1][=C][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 3.006076302628229e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Chlorobiphenyl\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H24NO4PS3/c1-12(2)18-20(21,19-13(3)4)22-11-10-15-23(16,17)14-8-6-5-7-9-14/h5-9,12-13,15H,10-11H2,1-4H3\\n\",\n        \"output\": \" Bensulide\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" ClC1CC2C(C1Cl)C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl\\n\",\n        \"output\": \" -6.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)CCOC=O\\n\",\n        \"output\": \" Isopentyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,4-Pentadiene \\n\",\n        \"output\": \" [C][=C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CNC(=O)Oc1cccc2CC(C)(C)Oc12\\n\",\n        \"output\": \" Carbofuran\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Spironolactone\\n\",\n        \"output\": \" InChI=1S/C24H32O4S/c1-14(25)29-19-13-15-12-16(26)4-8-22(15,2)17-5-9-23(3)18(21(17)19)6-10-24(23)11-7-20(27)28-24/h12,17-19,21H,4-11,13H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H6N2O4/c1-5-2-3-6(8(10)11)4-7(5)9(12)13/h2-4H,1H3\\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccc(I)cc1\\n\",\n        \"output\": \" p-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" o-Methoxyphenol\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pentachlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6HCl5/c7-2-1-3(8)5(10)6(11)4(2)9/h1H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Anthracene\\n\",\n        \"output\": \" -6.35\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Methoxychlor\\n\",\n        \"output\": \" 1.2882495516931348e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Methylbutan-2-ol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,4-Benzenediol\\n\",\n        \"output\": \" InChI=1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=O]\\n\",\n        \"output\": \" Quinonamid\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Phenylthiourea\\n\",\n        \"output\": \" NC(=S)Nc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1CCCCCC1\\n\",\n        \"output\": \" Cycloheptane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Fluvalinate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C2H6O/c1-2-3/h3H,2H2,1H3\\n\",\n        \"output\": \" 12.589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diethyl phthalate \\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Fenothiocarb\\n\",\n        \"output\": \" CN(C)C(=O)SCCCCOc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1N(COC(=O)CCCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3-Octanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCO\\n\",\n        \"output\": \" 1-Hexadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC=C(C)C\\n\",\n        \"output\": \" -2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/CH2Br2/c2-1-3/h1H2\\n\",\n        \"output\": \" Dibromomethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Etoposide (148-167,25mg/ml)\\n\",\n        \"output\": \" [C][O][C][=C][C][=Branch1][O][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][C][Branch1][#Branch1][C][O][C][Ring1][Branch1][=O][C][Branch2][Ring1][#Branch1][O][C][O][C][C][O][C][Branch1][C][C][O][C][Ring1][#Branch1][C][Branch1][C][O][C][Ring1][N][O][C][=C][C][O][C][O][C][=Ring1][Branch1][C][=C][Ring2][Ring1][#C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][/C][=C][/C]\\n\",\n        \"output\": \" 0.00015135612484362088 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=Cc1ccccc1\\n\",\n        \"output\": \" 0.06456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" Butethal\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Oc1cccc2ccccc12\\n\",\n        \"output\": \" 0.006025595860743574 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3\\n\",\n        \"output\": \" 7.585775750291836e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Carbanilide\\n\",\n        \"output\": \" InChI=1S/C13H12N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" p-Fluoroacetanilide\\n\",\n        \"output\": \" -1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)OC(=O)C\\n\",\n        \"output\": \" 0.28183829312644537 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][C][C][C][Branch1][Branch1][C][Ring1][Branch1][Cl][C][Branch1][C][Cl][C][=Branch2][Ring1][C][=C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][Branch2][Branch1][C][Cl][Cl][Cl]\\n\",\n        \"output\": \" Chlordane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2-Butoxyethanol\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][S][=Branch1][C][=O][S][C][C][=C]\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][Branch1][=N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Heptanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Mebendazole\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" BrCBr\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,3-Dichlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Dicofol\\n\",\n        \"output\": \" [O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3\\n\",\n        \"output\": \" -3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,3,5-Trichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(9)5(10)2-3/h1-2,10H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H\\n\",\n        \"output\": \" Coronene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Thiourea\\n\",\n        \"output\": \" NC(=S)N\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc2cc(C)ccc2c1\\n\",\n        \"output\": \" 2,6-Dimethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H15O2PS3/c1-4-11-5-6-12-9(10,7-2)8-3/h4-6H2,1-3H3\\n\",\n        \"output\": \" -3.091\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=Branch1][C][=S][N]\\n\",\n        \"output\": \" Thiourea\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1ccccc1Cl\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 5-Allyl-5-methylbarbital\\n\",\n        \"output\": \" InChI=1S/C8H10N2O3/c1-3-4-8(2)5(11)9-7(13)10-6(8)12/h3H,1,4H2,2H3,(H2,9,10,11,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)NC1CCCCCCC1\\n\",\n        \"output\": \" Cycluron\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1,2,3-Trimethylbenzene \\n\",\n        \"output\": \" 0.000630957344480193 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C3H8/c1-3-2/h3H2,1-2H3\\n\",\n        \"output\": \" 0.01148153621496883 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Methyl-3-hexanol\\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-4-6-7(3,8)5-2/h8H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pteridine\\n\",\n        \"output\": \" [C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.0969999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H19O6PS2/c1-5-15-9(11)7-8(10(12)16-6-2)19-17(18,13-3)14-4/h8H,5-7H2,1-4H3\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCOC(=O)c1ccccc1S(=O)(=O)NN(C=O)c2nc(Cl)cc(OC)n2\\n\",\n        \"output\": \" -4.5760000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Bromopentane\\n\",\n        \"output\": \" InChI=1S/C5H11Br/c1-2-3-4-5-6/h2-5H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,3,4-Trimethylpentane\\n\",\n        \"output\": \" InChI=1S/C8H18/c1-6(2)8(5)7(3)4/h6-8H,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c2ccc1ocnc1c2\\n\",\n        \"output\": \" Benzoxazole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OCC(O)C(O)CO\\n\",\n        \"output\": \" Erythritol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCO\\n\",\n        \"output\": \" 1-Butanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H18N4O2/c1-7-8(2)12-10(14(3)4)13-9(7)17-11(16)15(5)6/h1-6H3\\n\",\n        \"output\": \" Pirimicarb\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Decanone\\n\",\n        \"output\": \" CCCCCCCCC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,3-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 17a-Methyltestosterone\\n\",\n        \"output\": \" -3.9989999999999997\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" o-Hydroxybenzamide\\n\",\n        \"output\": \" -1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Nonanone\\n\",\n        \"output\": \" -2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 3-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Chlorobenzene\\n\",\n        \"output\": \" 0.004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dichlorophen\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3\\n\",\n        \"output\": \" 2-Propanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][Branch1][P][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][=C][Branch1][C][C][C][=C][Ring1][#C][C]\\n\",\n        \"output\": \" Mefluidide\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CCl4/c2-1(3,4)5\\n\",\n        \"output\": \" 0.004897788193684461 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCO\\n\",\n        \"output\": \" 1-Pentadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Eicosane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Diethyl phthalate \\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Phenylethanol\\n\",\n        \"output\": \" [C][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-Hydroxyacetanilide\\n\",\n        \"output\": \" CC(=O)Nc1ccc(O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pyrazon\\n\",\n        \"output\": \" [N][C][C][=N][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Ring1][=N][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" -2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" -2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/CH2Cl2/c2-1-3/h1H2\\n\",\n        \"output\": \" 0.2344228815319922 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H10/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" 4.518559443749226e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" t-Pentylbenzene\\n\",\n        \"output\": \" InChI=1S/C11H16/c1-11(2,3)9-10-7-5-4-6-8-10/h4-8H,9H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-3-4-5-6(7)8-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Oxadiazon\\n\",\n        \"output\": \" -5.696000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Norea\\n\",\n        \"output\": \" InChI=1S/C13H22N2O/c1-15(2)13(16)14-12-7-8-6-11(12)10-5-3-4-9(8)10/h8-12H,3-7H2,1-2H3,(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccoc1\\n\",\n        \"output\": \" 0.15135612484362082 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,2-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][C][C][Branch1][C][Cl][=C]\\n\",\n        \"output\": \" Sulfallate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Methylpentanol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC=C\\n\",\n        \"output\": \" Ethyl vinyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1ccc(Cl)c(Cl)c1Cl\\n\",\n        \"output\": \" -2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Azodrin\\n\",\n        \"output\": \" CNC(=O)C=C(C)OP(=O)(OC)OC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" -6.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Cc1c(cccc1N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Fenoxycarb\\n\",\n        \"output\": \" 1.9952623149688786e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H5Cl5/c13-6-4-9(16)12(10(17)5-6)11-7(14)2-1-3-8(11)15/h1-5H\\n\",\n        \"output\": \" 2,2,4,6,6'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][Br]\\n\",\n        \"output\": \" 1-Bromohexane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Pentachloroethane\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Salicylamide\\n\",\n        \"output\": \" InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Maltose\\n\",\n        \"output\": \" OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cn1c(=O)n(C)c2nc[nH]c2c1=O\\n\",\n        \"output\": \" -1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COc1nc(NC(C)C)nc(NC(C)C)n1\\n\",\n        \"output\": \" Prometon\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methy-2-Butene\\n\",\n        \"output\": \" 0.002754228703338166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H5BrO/c7-5-1-3-6(8)4-2-5/h1-4,8H\\n\",\n        \"output\": \" 4-Bromophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Thiourea\\n\",\n        \"output\": \" [N][C][=Branch1][C][=S][N]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ioxynil\\n\",\n        \"output\": \" Oc1c(I)cc(C#N)cc1I\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Tetradecane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Monuron\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C3H7I/c1-3(2)4/h3H,1-2H3\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methyl propionate\\n\",\n        \"output\": \" InChI=1S/C4H8O2/c1-3-4(5)6-2/h3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Bromooctane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethyl hexanoate\\n\",\n        \"output\": \" CCCCCC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C11H12N2O/c1-9-8-11(14)13(12(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3\\n\",\n        \"output\": \" 5.188000389289611 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dibutyl ether \\n\",\n        \"output\": \" CCCCOCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN1CC(O)N(C1=O)c2nnc(s2)C(C)(C)C\\n\",\n        \"output\": \" Buthidazole\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cn2c(=O)n(C)c1ncn(CC(O)CO)c1c2=O\\n\",\n        \"output\": \" Dyphylline\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Ethylnaphthalene \\n\",\n        \"output\": \" CCc1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][C]\\n\",\n        \"output\": \" -4.72\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,3-Dinitrobenzene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][S]\\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][C][C][Cl]\\n\",\n        \"output\": \" 0.023988329190194897 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its oil solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H10O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-6H,1-2H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3-Butanoyloxymethylphenytoin\\n\",\n        \"output\": \" [O][=C][N][Branch1][#Branch2][C][O][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2-Pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Nerol\\n\",\n        \"output\": \" CC(C)=CCC/C(C)=C\\\\CO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCC#C\\n\",\n        \"output\": \" -3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Phorate\\n\",\n        \"output\": \" InChI=1S/C7H17O2PS3/c1-4-8-10(11,9-5-2)13-7-12-6-3/h4-7H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4BrCl/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" m-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" difluron\\n\",\n        \"output\": \" InChI=1S/C14H9ClF2N2O2/c15-8-4-6-9(7-5-8)18-14(21)19-13(20)12-10(16)2-1-3-11(12)17/h1-7H,(H2,18,19,20,21)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 3-Pentanoyloxymethylphenytoin\\n\",\n        \"output\": \" 2.0989398836235246e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H9Cl5/c15-11-5-1-9(2-6-11)13(14(17,18)19)10-3-7-12(16)8-4-10/h1-8,13H\\n\",\n        \"output\": \" -7.15\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" FC(F)(Cl)C(F)(Cl)Cl\\n\",\n        \"output\": \" 0.0009120108393559096 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" butacarb\\n\",\n        \"output\": \" [C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][=C][C][Branch1][Branch2][O][C][=Branch1][C][=O][N][C][=C][Ring2][Ring1][Ring1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,3,4-Trimethylpentane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Medrogestone\\n\",\n        \"output\": \" CC(=O)C3(C)CCC4C2C=C(C)C1=CC(=O)CCC1(C)C2CCC34C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)OC(=O)C\\n\",\n        \"output\": \" Isopropyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC(=C)C(=C)C\\n\",\n        \"output\": \" -2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Propanil\\n\",\n        \"output\": \" CCC(=O)Nc1ccc(Cl)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" O=c2[nH]c1CCCc1c(=O)n2C3CCCCC3\\n\",\n        \"output\": \" -4.593999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)COC(=O)C\\n\",\n        \"output\": \" Isobutyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benzo(e)pyrene\\n\",\n        \"output\": \" InChI=1S/C20H12/c1-2-8-16-15(7-1)17-9-3-5-13-11-12-14-6-4-10-18(16)20(14)19(13)17/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Heptachlor\\n\",\n        \"output\": \" ClC1C=CC2C1C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Prednisolone\\n\",\n        \"output\": \" CC12CC(O)C3C(CCC4=CC(=O)C=CC34C)C2CCC1(O)C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" p-Bromoacetanilide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" benzoin\\n\",\n        \"output\": \" InChI=1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Abate\\n\",\n        \"output\": \" -6.237\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methyl formate\\n\",\n        \"output\": \" [C][O][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][Branch2][C][C][Branch1][C][O][C][O][C][=Ring1][#Branch2][C][Ring1][S][=O]\\n\",\n        \"output\": \" 0.6760829753919817 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Dimethyl sulfide\\n\",\n        \"output\": \" 0.35481338923357547 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Pyrolan\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H7I/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" 1-Iodonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCC(=O)C\\n\",\n        \"output\": \" 2-Hexanone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccccc1c2ccccc2\\n\",\n        \"output\": \" 2-Chlorobiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2-Benzenediol\\n\",\n        \"output\": \" InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pyridazine\\n\",\n        \"output\": \" InChI=1S/C4H4N2/c1-2-4-6-5-3-1/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dimefuron\\n\",\n        \"output\": \" InChI=1S/C15H19ClN4O3/c1-15(2,3)12-18-20(14(22)23-12)11-7-6-9(8-10(11)16)17-13(21)19(4)5/h6-8H,1-5H3,(H,17,21)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 7,12-Dimethylbenz(a)anthracene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring2][Ring1][Ring1][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccccc1N(=O)=O\\n\",\n        \"output\": \" o-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Deoxycorticosterone\\n\",\n        \"output\": \" InChI=1S/C21H30O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h11,15-18,22H,3-10,12H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C]\\n\",\n        \"output\": \" 0.3981071705534972 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" -0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4BrI/c7-5-1-3-6(8)4-2-5/h1-4H\\n\",\n        \"output\": \" -4.56\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethyl-p-aminobenzoate\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Bensulide\\n\",\n        \"output\": \" CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" p-Chloroiodobenzene\\n\",\n        \"output\": \" -4.03\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [S][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][Branch1][N][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Valeraldehyde\\n\",\n        \"output\": \" [C][C][C][C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1,1-Dichloroethylene\\n\",\n        \"output\": \" -1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Diuron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][C]\\n\",\n        \"output\": \" Diethyl ether \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" -3.11\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" L-arabinose\\n\",\n        \"output\": \" 2.4547089156850306 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Br][C][Branch1][C][Br][Branch1][C][Br][Br]\\n\",\n        \"output\": \" 0.0007244359600749898 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Fc1cccc(F)c1\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,3-Difluorobenzene\\n\",\n        \"output\": \" Fc1cccc(F)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H21O2PS3/c1-6-10-12(13,11-7-2)15-8-14-9(3,4)5/h6-8H2,1-5H3\\n\",\n        \"output\": \" Terbufos\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Mefenacet\\n\",\n        \"output\": \" [C][N][Branch2][Ring1][Ring2][C][=Branch1][C][=O][C][O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 6-methoxypteridine\\n\",\n        \"output\": \" [C][O][C][=C][N][=C][N][=C][N][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCc1ccccc1\\n\",\n        \"output\": \" Pentylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzylchloride\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C]\\n\",\n        \"output\": \" Azodrin\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1cccc(C)n1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Decanol\\n\",\n        \"output\": \" 0.00023442288153199226 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccncc1C\\n\",\n        \"output\": \" 3,4-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Indole\\n\",\n        \"output\": \" c2ccc1[nH]ccc1c2\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,2,4,6,6'-PCB\\n\",\n        \"output\": \" InChI=1S/C12H5Cl5/c13-6-4-9(16)12(10(17)5-6)11-7(14)2-1-3-8(11)15/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4ClNO2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H\\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Diethyl ether \\n\",\n        \"output\": \" [C][C][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Butoxyethanol\\n\",\n        \"output\": \" CCCCOCCO\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methyl propyl ether \\n\",\n        \"output\": \" [C][C][C][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Isoquinoline\\n\",\n        \"output\": \" [C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3\\n\",\n        \"output\": \" 3-Methylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1-Iodopropane\\n\",\n        \"output\": \" -2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Bromobutane\\n\",\n        \"output\": \" [C][C][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9998618696327446e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCC(CC)CO\\n\",\n        \"output\": \" -2.11\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cyclobutyl-5-spirobarbituric acid\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=Branch1][C][=O][N][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methyltetrahydrofurane\\n\",\n        \"output\": \" InChI=1S/C5H10O/c1-5-3-2-4-6-5/h5H,2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Di(2-ethylhexyl)-phthalate\\n\",\n        \"output\": \" CCCCC(CC)COC(=O)c1ccccc1C(=O)OCC(CC)CCCC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H13NO2/c1-2-7-13-10(12)8-3-5-9(11)6-4-8/h3-6H,2,7,11H2,1H3\\n\",\n        \"output\": \" -2.452\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Isopropyl acetate\\n\",\n        \"output\": \" InChI=1S/C5H10O2/c1-4(2)7-5(3)6/h4H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1(O)c(C)ccc(C(C)C)c1\\n\",\n        \"output\": \" -2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1CCC=CCC1\\n\",\n        \"output\": \" Cycloheptene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][C][Cl]\\n\",\n        \"output\": \" 1,2-Dichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,4-Diethylbenzene \\n\",\n        \"output\": \" InChI=1S/C10H14/c1-3-9-5-7-10(4-2)8-6-9/h5-8H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H7NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-6H,(H,9,10,11)\\n\",\n        \"output\": \" 0.001169499391019871 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Simetryn\\n\",\n        \"output\": \" CSc1nc(nc(n1)N(C)C)N(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H6/c1-3-4-2/h1H,4H2,2H3\\n\",\n        \"output\": \" 1-Butyne\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Nonane\\n\",\n        \"output\": \" InChI=1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility of given compound in room temperature. ->\",\n        \"input\": \" Methyl acrylate\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H14N2O3/c1-4-9(5(2)3)6(12)10-8(14)11-7(9)13/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" -2.148\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,5-Dimethlnapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC=C)CC=C\\n\",\n        \"output\": \" 5,5-Diallylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Fluorometuron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Nitromethane\\n\",\n        \"output\": \" InChI=1S/CH3NO2/c1-2(3)4/h1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H15NO2/c1-8(2)9-6-4-5-7-10(9)14-11(13)12-3/h4-8H,1-3H3,(H,12,13)\\n\",\n        \"output\": \" -2.863\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,1-Dichloroethylene\\n\",\n        \"output\": \" [Cl][C][=Branch1][C][=C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][O][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.344228815319923e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][C][C][Branch1][C][C][C][C][C][C][C][Branch1][C][C][C][Branch1][C][C][C][C][O][C][C][Branch1][C][C][C][C][Ring1][#Branch1][O][C][Ring1][N][C][C][Ring1][S][C][Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=C]\\n\",\n        \"output\": \" Diosgenin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Iodofenphos\\n\",\n        \"output\": \" InChI=1S/C8H8Cl2IO3PS/c1-12-15(16,13-2)14-8-4-5(9)7(11)3-6(8)10/h3-4H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" 0.00015848931924611142 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Ring2][C][=Branch1][C][=O][C][O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.873\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dimecron\\n\",\n        \"output\": \" InChI=1S/C10H19ClNO5P/c1-5-12(6-2)10(13)9(11)7-8-17-18(14,15-3)16-4/h7H,5-6,8H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C2NC(=O)C1(CCC1)C(=O)N2\\n\",\n        \"output\": \" Cyclobutyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC=C(CC)C=O\\n\",\n        \"output\": \" 2-Ethyl-2-hexanal\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCOCC\\n\",\n        \"output\": \" 0.21877616239495523 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H12/c1-2-10-7-8-11-5-3-4-6-12(11)9-10/h3-9H,2H2,1H3\\n\",\n        \"output\": \" -4.29\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][C][C][C][C][Branch1][=Branch1][C][Ring1][=Branch2][=Ring1][Branch1][=C][Ring1][N][C][=C][Ring1][S]\\n\",\n        \"output\": \" 1.202264434617413e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 5-Allyl-5-phenylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC=C)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 4-Methylpentanol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 5,5-Diisopropylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C]\\n\",\n        \"output\": \" 0.01778279410038923 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" -8.94\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Trichloroethylene\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H3I2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H\\n\",\n        \"output\": \" Ioxynil\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H9Cl/c1-3-4(2)5/h4H,3H2,1-2H3\\n\",\n        \"output\": \" 2-Chlorobutane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Iodopropane\\n\",\n        \"output\": \" [C][C][C][I]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,3-Dichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3\\n\",\n        \"output\": \" -5.03\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Ethyl vinyl ether\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" p-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Talbutal\\n\",\n        \"output\": \" 0.009638290236239706 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Brc1cc(Br)cc(Br)c1\\n\",\n        \"output\": \" 2.5118864315095823e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][Branch1][C][F][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][N][Ring1][#Branch1][C][C][Ring2][Ring1][C][C][C][Branch1][C][O][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" -3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC/C=C\\\\C\\n\",\n        \"output\": \" cis-2-Pentene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(8)5(10)6(11)4(2)9/h1,11H\\n\",\n        \"output\": \" 2,3,5,6-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][C][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H24O/c1-3-4-5-6-7-8-9-10-11(2)12/h11-12H,3-10H2,1-2H3\\n\",\n        \"output\": \" 2-Undecanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CNc1ccccc1\\n\",\n        \"output\": \" N-Methylaniline \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N][C][C][O][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N]\\n\",\n        \"output\": \" Fenoxycarb\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OC1CCCCC1\\n\",\n        \"output\": \" Cyclohexanol \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 1,3-Difluorobenzene\\n\",\n        \"output\": \" 0.01 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC1=C(SCCO1)C(=O)Nc2ccccc2\\n\",\n        \"output\": \" 0.0007244359600749898 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][\\\\C][=C][/Cl]\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Nonanol\\n\",\n        \"output\": \" 0.000977237220955811 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Butamben\\n\",\n        \"output\": \" CCCCOC(=O)c1ccc(N)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][=C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" Prasterone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCOC(=O)c1ccccc1C(=O)OCCCCCC\\n\",\n        \"output\": \" Dihexyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Heptanoyloxymethylphenytoin\\n\",\n        \"output\": \" InChI=1S/C23H26N2O4/c1-2-3-4-11-16-20(26)29-17-25-21(27)23(24-22(25)28,18-12-7-5-8-13-18)19-14-9-6-10-15-19/h5-10,12-15H,2-4,11,16-17H2,1H3,(H,24,28)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCO\\n\",\n        \"output\": \" 0.251188643150958 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" 0.00027478941531023943 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Kepone\\n\",\n        \"output\": \" InChI=1S/C10Cl10O/c11-2-1(21)3(12)6(15)4(2,13)8(17)5(2,14)7(3,16)9(6,18)10(8,19)20\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chloropicrin\\n\",\n        \"output\": \" InChI=1S/CCl3NO2/c2-1(3,4)5(6)7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O]\\n\",\n        \"output\": \" Testosterone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 4.5708818961487516e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C27H37FO6/c1-5-6-7-23(33)34-27(22(32)15-29)16(2)12-20-19-9-8-17-13-18(30)10-11-24(17,3)26(19,28)21(31)14-25(20,27)4/h10-11,13,16,19-21,29,31H,5-9,12,14-15H2,1-4H3\\n\",\n        \"output\": \" Betamethasone-17-valerate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4-Chloroanisole\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1c(I)cc(C#N)cc1I\\n\",\n        \"output\": \" Ioxynil\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fluorene \\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Procymidone\\n\",\n        \"output\": \" CC12CC2(C)C(=O)N(C1=O)c3cc(Cl)cc(Cl)c3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" m-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" 5-Ethyl-5-(3-methylbutyl)barbital\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C3H7Br/c1-3(2)4/h3H,1-2H3\\n\",\n        \"output\": \" 0.025703957827688632 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 3.63078054770101e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Diiodomethane\\n\",\n        \"output\": \" [I][C][I]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C3H8O/c1-3(2)4/h3-4H,1-2H3\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" o-Toluidine\\n\",\n        \"output\": \" 0.006165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][#C]\\n\",\n        \"output\": \" 1-Octyne \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H14O/c8-7-5-3-1-2-4-6-7/h7-8H,1-6H2\\n\",\n        \"output\": \" 0.1318256738556407 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethyl heptanoate\\n\",\n        \"output\": \" InChI=1S/C9H18O2/c1-3-5-6-7-8-9(10)11-4-2/h3-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Chloramphenicol\\n\",\n        \"output\": \" -2.1109999999999998\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][Br]\\n\",\n        \"output\": \" -3.81\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Phthalonitrile\\n\",\n        \"output\": \" 0.004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C17H12Cl2N4/c1-10-21-22-16-9-20-17(12-4-2-3-5-14(12)19)13-8-11(18)6-7-15(13)23(10)16/h2-8H,9H2,1H3\\n\",\n        \"output\": \" Triazolam\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" 2-Methylpropene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H8/c1-4-5(2)3/h4H,1-2H2,3H3\\n\",\n        \"output\": \" 2-Methyl-1,3-Butadiene \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1C=CCC=C1\\n\",\n        \"output\": \" 1,4-Cyclohexadiene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" -2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=Branch1][C][=O][NH1][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" Flucytosine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COc1cc(CC=C)ccc1O\\n\",\n        \"output\": \" Eugenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl]\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCOC(=O)CCC\\n\",\n        \"output\": \" Ethyl pentanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -5.736000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Trichloroacetonitrile\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][#N]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2-Diethylbenzene\\n\",\n        \"output\": \" InChI=1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCOC(=O)NCCOc2ccc(Oc1ccccc1)cc2\\n\",\n        \"output\": \" -4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 8.709635899560814e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" c1ccccc1C(O)C(O)c2ccccc2\\n\",\n        \"output\": \" 0.011748975549395297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H18N2O3/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" D-fenchone\\n\",\n        \"output\": \" CC2(C)C1CCC(C)(C1)C2=O\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Pentadecanol\\n\",\n        \"output\": \" InChI=1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" c1c(O)C2C(=O)C3cc(O)ccC3OC2cc1(OC)\\n\",\n        \"output\": \" -2.943\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" o-Chlorobromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4BrCl/c7-5-3-1-2-4-6(5)8/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Ethyl pyridine\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCC(C)(O)CC\\n\",\n        \"output\": \" 3-Methyl-3-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanone\\n\",\n        \"output\": \" InChI=1S/C7H14O/c1-5(2)7(8)6(3)4/h5-6H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" COCCCNc1nc(NC(C)C)nc(SC)n1\\n\",\n        \"output\": \" -2.928\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#C]\\n\",\n        \"output\": \" 5-Methylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2-Dimethylpentanol\\n\",\n        \"output\": \" CCCC(C)(C)CO\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Hydroxybenzaldehyde \\n\",\n        \"output\": \" InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H18/c1-7-8(2)10(4)12(6)11(5)9(7)3/h1-6H3\\n\",\n        \"output\": \" 5.888436553555884e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" m-Nitrotoluene\\n\",\n        \"output\": \" Cc1cccc(c1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=Cc1ccccc1\\n\",\n        \"output\": \" Benzaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1ccc2cc(C)ccc2c1\\n\",\n        \"output\": \" -4.89\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Triamcinolone\\n\",\n        \"output\": \" InChI=1S/C21H27FO6/c1-18-6-5-12(24)7-11(18)3-4-13-14-8-15(25)21(28,17(27)10-23)19(14,2)9-16(26)20(13,18)22/h5-7,13-16,23,25-26,28H,3-4,8-10H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1ccc2c(c1)c3cccc4c3c2cc5ccccc54\\n\",\n        \"output\": \" Benzo(b)fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H14NO5PS/c1-3-14-17(18,15-4-2)16-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" 2.187761623949552e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1CCCCC1\\n\",\n        \"output\": \" Cyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCC(C)C(C)C\\n\",\n        \"output\": \" 5.248074602497723e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(=O)CC\\n\",\n        \"output\": \" 3-Hexanone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" 5.888436553555884e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Oc1c(Cl)c(Cl)cc(Cl)c1Cl\\n\",\n        \"output\": \" 0.00042657951880159257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H18O/c1-3-4-5-6-7-8-9(2)10/h3-8H2,1-2H3\\n\",\n        \"output\": \" 2-Nonanone\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Monuron\\n\",\n        \"output\": \" InChI=1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethyne\\n\",\n        \"output\": \" C#C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H15ClO4/c1-11(21)10-15(12-6-8-13(20)9-7-12)17-18(22)14-4-2-3-5-16(14)24-19(17)23/h2-9,15,22H,10H2,1H3\\n\",\n        \"output\": \" Coumachlor\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 1.4125375446227544 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2,3,4-Trichlorophenol\\n\",\n        \"output\": \" 0.0021379620895022326 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][S][C]\\n\",\n        \"output\": \" thioanisole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H19Cl2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\",\n        \"output\": \" Cypermethrin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chlorbromuron\\n\",\n        \"output\": \" InChI=1S/C9H10BrClN2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 4-Ethyltoluene\\n\",\n        \"output\": \" InChI=1S/C9H12/c1-3-9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H12/c1-7-4-8(2)6-9(3)5-7/h4-6H,1-3H3\\n\",\n        \"output\": \" -3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" N#Cc1ccccc1\\n\",\n        \"output\": \" 0.1 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\\n\",\n        \"output\": \" p,p'-Biphenyldiamine \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethylbenzene\\n\",\n        \"output\": \" InChI=1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-3-7(2)5-8(9)4-6/h3-5,9H,1-2H3\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-5-13-6-2-11-17-18-12-4-8-14-7-3-10-16(20(14)18)15(9-1)19(13)17/h1-12H\\n\",\n        \"output\": \" Perylene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" -1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-4-5-6-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" 0.10232929922807542 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Propane\\n\",\n        \"output\": \" [C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" Etofenprox\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-7-14-13(6-1)12-19-16-9-4-3-8-15(16)18-11-5-10-17(14)20(18)19/h1-12H\\n\",\n        \"output\": \" 5.888436553555884e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C18H18O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h2-5,10,16,19H,6-9H2,1H3\\n\",\n        \"output\": \" -5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Octanol\\n\",\n        \"output\": \" CCCCCCC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)NC(=O)N1CC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2\\n\",\n        \"output\": \" 4.2072662838444376e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanol\\n\",\n        \"output\": \" 0.06025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.03235936569296283 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Eugenol\\n\",\n        \"output\": \" 0.02754228703338166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Chlorobromobenzene\\n\",\n        \"output\": \" Clc1ccc(Br)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4N4O/c11-6-9-3-4-5(10-6)8-2-1-7-4/h1-3H,(H,8,9,10,11)\\n\",\n        \"output\": \" -1.9469999999999998\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Isobutyl acetate\\n\",\n        \"output\": \" 0.06165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Chlorbromuron\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)C(C)C(C)C\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ditalimfos\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=N(=O)c1cccc2ccccc12\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Chlorobromobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 5-Ethyl-5-isopropylbarbituric acid\\n\",\n        \"output\": \" 0.0071121351365332885 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" brompyrazone\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][N][N][=C][C][Branch1][C][N][=C][Branch1][C][Br][C][Ring1][Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCN(CC)c1c(cc(c(N)c1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" -5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Diphenyl ether \\n\",\n        \"output\": \" O(c1ccccc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][#C]\\n\",\n        \"output\": \" 1-Butyne\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" m-Chloronitrobenzene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][N][C]\\n\",\n        \"output\": \" 5.188000389289611 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)Oc1cc(c(Cl)cc1Cl)n2nc(oc2=O)C(C)(C)C\\n\",\n        \"output\": \" Oxadiazon\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Methyl-2-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Valeraldehyde\\n\",\n        \"output\": \" InChI=1S/C5H10O/c1-2-3-4-5-6/h5H,2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C\\n\",\n        \"output\": \" Piperophos\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3\\n\",\n        \"output\": \" 1-Nonanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dyphylline\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][Branch2][C][C][Branch1][C][O][C][O][C][=Ring1][#Branch2][C][Ring1][S][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 3-Butanoyloxymethylphenytoin\\n\",\n        \"output\": \" 8.491804750363127e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCC(=O)OCC\\n\",\n        \"output\": \" Ethyl hexanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccccc1\\n\",\n        \"output\": \" Fenuron\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1N(COC(=O)CCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3-Pentanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Heptanol\\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-2-3-4-5-6-7-8/h8H,2-7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9H\\n\",\n        \"output\": \" Indole\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-4-5(2)3/h2,4H2,1,3H3\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Stirofos\\n\",\n        \"output\": \" 3.006076302628229e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cycloheptane\\n\",\n        \"output\": \" -3.51\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c2ccc1[nH]nnc1c2\\n\",\n        \"output\": \" Benzotriazole\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][O][C][C][Ring1][#Branch1][C][C][C][C][Ring1][O][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][=O]\\n\",\n        \"output\": \" 3.9627803425543934e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H6N2O5/c1-4-2-5(8(11)12)3-6(7(4)10)9(13)14/h2-3,10H,1H3\\n\",\n        \"output\": \" 0.03499451670283573 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3,3-Dimethylpentane\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1,2-Dichloropropane\\n\",\n        \"output\": \" -1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(C)c(Cl)c1\\n\",\n        \"output\": \" Chlortoluron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCCC(=O)OCC\\n\",\n        \"output\": \" 7.943282347242822e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [I][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Iodonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][=C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][=C][Ring2][Ring1][N]\\n\",\n        \"output\": \" diisooctyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H10Cl2N2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\",\n        \"output\": \" 0.00025585858869056453 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzamide\\n\",\n        \"output\": \" NC(=O)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=C2NC(=O)C1(CCCCCCC1)C(=O)N2\\n\",\n        \"output\": \" -2.9819999999999998\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" Azobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Isoproturon\\n\",\n        \"output\": \" InChI=1S/C12H18N2O/c1-9(2)10-5-7-11(8-6-10)13-12(15)14(3)4/h5-9H,1-4H3,(H,13,15)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H11ClN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\\n\",\n        \"output\": \" Monolinuron\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" 0.003404081897010009 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" c1ccc2c(c1)ccc3ccccc32\\n\",\n        \"output\": \" 5.4954087385762485e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 1,7-phenantroline\\n\",\n        \"output\": \" 0.0020892961308540386 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H11N3O3/c19-14-9-16-15(10-4-2-1-3-5-10)12-8-11(18(20)21)6-7-13(12)17-14/h1-8H,9H2,(H,17,19)\\n\",\n        \"output\": \" Nitrazepam\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][C][O]\\n\",\n        \"output\": \" 3,3-Dimethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1ccc(C)cc1\\n\",\n        \"output\": \" -2.77\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-6(4-2)5-7/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 2-Ethylbutanal\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H15NO3/c1-12(2)7-8-5-4-6-9(10(8)16-12)15-11(14)13-3/h4-6H,7H2,1-3H3,(H,13,14)\\n\",\n        \"output\": \" 0.001584893192461114 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC12CC2(C)C(=O)N(C1=O)c3cc(Cl)cc(Cl)c3\\n\",\n        \"output\": \" Procymidone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][#C]\\n\",\n        \"output\": \" 0.004365158322401661 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-5-7(4)6(2)3/h6-7H,5H2,1-4H3\\n\",\n        \"output\": \" 2,3-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COP(=S)(OC)SCC(=O)N(C(C)C)c1ccc(Cl)cc1\\n\",\n        \"output\": \" 3.698281797802666e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-\\n\",\n        \"output\": \" cis 1,2-Dichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCCCCCC#C\\n\",\n        \"output\": \" -3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H\\n\",\n        \"output\": \" Thiophene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-4(2)6-3-5/h3-4H,1-2H3\\n\",\n        \"output\": \" -0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=C]\\n\",\n        \"output\": \" 1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 4-Nitroacetanilide\\n\",\n        \"output\": \" CC(=O)Nc1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClCC(C)C\\n\",\n        \"output\": \" 1-Chloro-2-methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Trichloromethane\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H6ClN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2\\n\",\n        \"output\": \" o-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,2,3,5-Tetrachlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)5(9)2-3/h1-2H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,1,1,2-Tetrachloroethane\\n\",\n        \"output\": \" [Cl][C][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][NH1][C][C][C][C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][#Branch2][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.593999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Riboflavin\\n\",\n        \"output\": \" [C][C][=C][C][N][=C][C][=Branch1][C][=O][NH1][C][=Branch1][C][=O][N][=C][Ring1][Branch2][N][Branch1][S][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O][C][=Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][=Branch2][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Hexanone\\n\",\n        \"output\": \" CCCC(=O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Propanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\\n\",\n        \"output\": \" Lactose\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CN(C)C(=O)NC1CCCCCCC1\\n\",\n        \"output\": \" -2.218\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCC(C)(C)O\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC1(OC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2)C=C\\n\",\n        \"output\": \" 1.188502227437019e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanone\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)(C)CO\\n\",\n        \"output\": \" 2,2-Dimethylpropanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Salicin\\n\",\n        \"output\": \" OCC2OC(Oc1ccccc1CO)C(O)C(O)C2O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/CHBr3/c2-1(3)4/h1H\\n\",\n        \"output\": \" Tribromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Clc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" -5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Methylbutan-2-ol\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H18N2O3/c1-2-14(11(17)15-13(19)16-12(14)18)10-6-4-8-3-5-9(10)7-8/h6,8-9H,2-5,7H2,1H3,(H2,15,16,17,18,19)\\n\",\n        \"output\": \" Reposal\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][Branch1][C][O][=C][Branch1][C][O][C][O][C][C][Branch1][C][O][C][C][=C][C][=Branch1][C][=O][C][Branch1][C][O][=C][C][Ring1][Branch2][=C][Ring1][N][C][=Ring1][S][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" hematein\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Benzoxazole\\n\",\n        \"output\": \" [C][=C][C][=C][O][C][=N][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCOC(=O)c1ccccc1C(=O)OCCCCCC\\n\",\n        \"output\": \" -6.144\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCC(=O)C\\n\",\n        \"output\": \" 2-Octanone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CN(C(=O)NC(C)(C)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" -3.35\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" o-Fluorobromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4BrF/c7-5-3-1-2-4-6(5)8/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzotriazole\\n\",\n        \"output\": \" [C][=C][C][=C][NH1][N][=N][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 1,1,1-Trichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3,3-Dimethyl-1-butanol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][Branch1][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2.6915348039269156 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(Sc2ccc(OP(=S)(OC)OC)cc2)cc1\\n\",\n        \"output\": \" Abate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Aminophenol\\n\",\n        \"output\": \" InChI=1S/C6H7NO/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Butyne\\n\",\n        \"output\": \" 0.057543993733715694 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H12/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1-10H,11H2\\n\",\n        \"output\": \" Diphenylmethane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Dapsone\\n\",\n        \"output\": \" InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/CCl3NO2/c2-1(3,4)5(6)7\\n\",\n        \"output\": \" Chloropicrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC(=O)CCN(SN(C)C(=O)Oc1cccc2CC(C)(C)Oc21)C(C)C\\n\",\n        \"output\": \" 1.9498445997580456e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][C][O][Ring1][Branch1]\\n\",\n        \"output\": \" -1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzo(b)fluorene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][P][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" ClCc1ccccc1\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H42O3/c1-16-9-22-23(29-15-16)14-27(4)24(30-22)12-21-20-11-18-10-19(28)6-7-25(18,2)13-17(20)5-8-26(21,27)3/h11,16-17,19-24,28H,5-10,12-15H2,1-4H3\\n\",\n        \"output\": \" Diosgenin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Nonanone\\n\",\n        \"output\": \" InChI=1S/C9H18O/c1-3-4-5-6-7-8-9(2)10/h3-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H7NO/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2\\n\",\n        \"output\": \" o-Aminophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Propylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzonitrile\\n\",\n        \"output\": \" [N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC1(C(=O)NCNC1=O)c2ccccc2\\n\",\n        \"output\": \" Primidone\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fenoxycarb\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][N][C][C][O][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Chloronapthalene\\n\",\n        \"output\": \" InChI=1S/C10H7Cl/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Mefluidide\\n\",\n        \"output\": \" CC(=O)Nc1cc(NS(=O)(=O)C(F)(F)F)c(C)cc1C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][N][C][=Branch1][C][=O][N][C][Branch1][Branch2][N][C][=Branch1][C][=O][O][C][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.883\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 4-hexylresorcinol\\n\",\n        \"output\": \" c1(O)cc(O)ccc1CCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cyclohexane\\n\",\n        \"output\": \" -3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][O][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][C][Branch1][#Branch1][C][O][C][Ring1][Branch1][=O][C][Branch2][Ring1][#Branch1][O][C][O][C][C][O][C][Branch1][C][C][O][C][Ring1][#Branch1][C][Branch1][C][O][C][Ring1][N][O][C][=C][C][O][C][O][C][=Ring1][Branch1][C][=C][Ring2][Ring1][#C][Ring1][=Branch2]\\n\",\n        \"output\": \" Etoposide (148-167,25mg/ml)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 2,3',4',5-PCB\\n\",\n        \"output\": \" 5.6234132519034905e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COC(=O)c1ccc(O)cc1\\n\",\n        \"output\": \" Methylparaben\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Parathion\\n\",\n        \"output\": \" CCOP(=S)(OCC)Oc1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H20O2/c1-3-4-5-6-7-8-9-10(11)12-2/h3-9H2,1-2H3\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][C][=O][C][C][Branch1][C][C][C][Ring1][Branch2][O][C][=C][Branch1][C][Cl][C][Branch1][Ring1][O][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][O][C][Ring1][=C][=O]\\n\",\n        \"output\": \" Griseofulvin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H8/c1-3-4-2/h3H,1,4H2,2H3\\n\",\n        \"output\": \" 1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl propyl ether\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-3-5-6-4-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,1,1,2-Tetrachloroethane\\n\",\n        \"output\": \" InChI=1S/C2H2Cl4/c3-1-2(4,5)6/h1H2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CNC(=O)C=C(C)OP(=O)(OC)OC\\n\",\n        \"output\": \" 4.477133041763624 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\\n\",\n        \"output\": \" Salicylamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][=C][Ring1][Branch2][C]\\n\",\n        \"output\": \" 2.5703957827688645e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Secobarbital\\n\",\n        \"output\": \" 0.0044055486350655345 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Atratone\\n\",\n        \"output\": \" InChI=1S/C9H17N5O/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" brompyrazone\\n\",\n        \"output\": \" 0.0007464487584100669 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/CHBr2Cl/c2-1(3)4/h1H\\n\",\n        \"output\": \" -1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" 0.00020417379446695296 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H14ClN5/c1-4-10-7-12-6(9)13-8(14-7)11-5(2)3/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" 0.0001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring1][=Branch1][Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 5.248074602497723e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Bromochloromethane\\n\",\n        \"output\": \" 0.1288249551693134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H17ClN2O4/c20-12-5-6-14-17(7-8-21-18(14)9-12)22-16-4-2-1-3-15(16)19(25)26-11-13(24)10-23/h1-9,13,23-24H,10-11H2,(H,21,22)\\n\",\n        \"output\": \" -4.571000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 4-Isopropyltoluene\\n\",\n        \"output\": \" CC(C)c1ccc(C)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4ClI/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" -3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][Ring2][Ring1][#Branch1][Branch1][C][C][C]\\n\",\n        \"output\": \" -6.025\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H13Cl/c1-2-3-4-5-6-7/h2-6H2,1H3\\n\",\n        \"output\": \" -3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 3.235936569296281e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\\n\",\n        \"output\": \" 0.01458814260275349 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 8.317637711026709e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Chloro-2-methylbutane\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][Branch1][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][N][C][=Branch1][C][=O][N][C][N][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Primidone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H\\n\",\n        \"output\": \" 0.046773514128719815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3,5-Dimethylphenol\\n\",\n        \"output\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][O][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Sulfanilamide\\n\",\n        \"output\": \" Nc1ccc(cc1)S(N)(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.003090295432513592 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C14H18N2O3/c1-2-14(11(17)15-13(19)16-12(14)18)10-6-4-8-3-5-9(10)7-8/h6,8-9H,2-5,7H2,1H3,(H2,15,16,17,18,19)\\n\",\n        \"output\": \" -2.696\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClC(Cl)=C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" P,P'-DDE\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][#Branch1][N][C][Branch1][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -4.194\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccccc1Br\\n\",\n        \"output\": \" -3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C=CC=C\\n\",\n        \"output\": \" 1,3-Butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H12N2O3/c1-3-8(4-2)5(11)9-7(13)10-6(8)12/h3-4H2,1-2H3,(H2,9,10,11,12,13)\\n\",\n        \"output\": \" -2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H18N4O6S/c1-3-5-14(6-4-2)12-10(15(17)18)7-9(23(13,21)22)8-11(12)16(19)20/h7-8H,3-6H2,1-2H3,(H2,13,21,22)\\n\",\n        \"output\": \" 6.9183097091893625e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dibenzofurane\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Vinclozolin\\n\",\n        \"output\": \" [C][C][Branch2][Ring1][O][O][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H21NOS/c1-4-7-8-11(6-3)10(12)13-9-5-2/h4-9H2,1-3H3\\n\",\n        \"output\": \" Pebulate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Phenanthrene\\n\",\n        \"output\": \" 5.4954087385762485e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 0.0034673685045253167 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Niridazole\\n\",\n        \"output\": \" O=C1NCCN1c2ncc(s2)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Napthacene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][C][Ring1][=C][=C][Ring2][Ring1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\\n\",\n        \"output\": \" -3.483\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCOC(=O)CC(=O)OCC\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][Branch1][C][Cl][=C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Triallate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Pentene \\n\",\n        \"output\": \" InChI=1S/C5H10/c1-3-5-4-2/h3H,1,4-5H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(=O)=O\\n\",\n        \"output\": \" Nitromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Ethyl pentanoate\\n\",\n        \"output\": \" 0.01778279410038923 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Sparsomycin (3,8mg/ml)\\n\",\n        \"output\": \" CSCS(=O)CC(CO)NC(=O)C=Cc1c(C)[nH]c(=O)[nH]c1=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Triazolam\\n\",\n        \"output\": \" Cc3nnc4CN=C(c1ccccc1Cl)c2cc(Cl)ccc2n34\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccc(Br)cc1\\n\",\n        \"output\": \" p-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Heptanol \\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-3-5-6-7(8)4-2/h7-8H,3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" 5-(3-Methyl-2-butenyl)-5-isoPrbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Methyl-1-Butene\\n\",\n        \"output\": \" InChI=1S/C5H10/c1-4-5(2)3/h4-5H,1H2,2-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCN(CC)C(=S)SCC(Cl)=C\\n\",\n        \"output\": \" Sulfallate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dinitramine\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Hexylbenzene \\n\",\n        \"output\": \" CCCCCCc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Succinimide\\n\",\n        \"output\": \" [O][=C][C][C][C][=Branch1][C][=O][N][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H13Br/c1-2-3-4-5-6-7/h2-6H2,1H3\\n\",\n        \"output\": \" -3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methylphenol\\n\",\n        \"output\": \" InChI=1S/C7H8O/c1-6-4-2-3-5-7(6)8/h2-5,8H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,2-Diethoxyethane \\n\",\n        \"output\": \" CCOCCOCC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" O=C1N(COC(=O)C)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3.3884415613920276e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][N][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Flucythrinate\\n\",\n        \"output\": \" CC(C)C(C(=O)OC(C#N)c1cccc(Oc2ccccc2)c1)c3ccc(OC(F)F)cc3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Cyclooctane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CSc1nc(nc(n1)N(C)C)N(C)C\\n\",\n        \"output\": \" -2.676\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H14N2O3/c1-4-9(5(2)3)6(12)10-8(14)11-7(9)13/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" 5-Ethyl-5-isopropylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1NCCN1c2ncc(s2)N(=O)=O\\n\",\n        \"output\": \" 0.0006025595860743575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3,3-Dimethyl-1-butanol\\n\",\n        \"output\": \" 0.31622776601683794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3\\n\",\n        \"output\": \" -2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Androsterone\\n\",\n        \"output\": \" InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Methyl butyrate\\n\",\n        \"output\": \" InChI=1S/C6H12O2/c1-3-5-8-6(7)4-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" o-Fluorobromobenzene\\n\",\n        \"output\": \" -2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1CCCCC1NC(=O)Nc2ccccc2\\n\",\n        \"output\": \" Siduron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 4-Nitroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [I][C][I]\\n\",\n        \"output\": \" Diiodomethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Phenylthiourea\\n\",\n        \"output\": \" -1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Chloro-2-bromoethane\\n\",\n        \"output\": \" [Cl][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanol\\n\",\n        \"output\": \" [C][C][Branch1][C][O][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Ethyl-1-hexanol\\n\",\n        \"output\": \" CCCCC(CC)CO\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Fluometuron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCNc1nc(NC(C)C)nc(OC)n1\\n\",\n        \"output\": \" -2.084\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Cl]\\n\",\n        \"output\": \" 1-Chlorohexane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H16/c1-3-5-7-6-4-2/h3-7H2,1-2H3\\n\",\n        \"output\": \" Heptane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-6(7)5(2)3/h5-7H,4H2,1-3H3\\n\",\n        \"output\": \" 2-Methyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H2\\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Butan-2-ol\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 1,1,1,2-Tetrachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" Triclosan\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC=C(Cl)Cl\\n\",\n        \"output\": \" Trichloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)C(C)(C)C\\n\",\n        \"output\": \" -4.36\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methane\\n\",\n        \"output\": \" [C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" N-Ethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 7-methoxypteridine\\n\",\n        \"output\": \" [C][O][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethylcyclohexane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][Branch1][=C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][P][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Octanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 2-Methylpropan-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Fenothiocarb\\n\",\n        \"output\": \" InChI=1S/C13H19NO2S/c1-14(2)13(15)17-11-7-6-10-16-12-8-4-3-5-9-12/h3-5,8-9H,6-7,10-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C=Cc1ccccc1\\n\",\n        \"output\": \" Styrene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Erythritol\\n\",\n        \"output\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Sulfallate\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][C][C][Branch1][C][Cl][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CN(C(=O)COc1nc2ccccc2s1)c3ccccc3\\n\",\n        \"output\": \" Mefenacet\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O]\\n\",\n        \"output\": \" Sorbitol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 0.000630957344480193 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCN(CC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" -5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(C)(C)CC\\n\",\n        \"output\": \" 3,3-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccccc1C2=NCC(=O)Nc3ccc(cc23)N(=O)=O\\n\",\n        \"output\": \" -3.4989999999999997\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2-Nonanone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C21H16/c1-13-5-8-17-15(11-13)7-9-18-19-10-6-14-3-2-4-16(21(14)19)12-20(17)18/h2-5,7-9,11-12H,6,10H2,1H3\\n\",\n        \"output\": \" 3-Methylcholanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2\\n\",\n        \"output\": \" Salicin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -4.36\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO\\n\",\n        \"output\": \" Hydrocortisone \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" Carbazole\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Isobutyl formate\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Undecanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/CHCl3/c2-1(3)4/h1H\\n\",\n        \"output\": \" Trichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][N][Branch1][#C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring1][=C][=O]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C][C][C]\\n\",\n        \"output\": \" -3.8960000000000004\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C3H7I/c1-2-3-4/h2-3H2,1H3\\n\",\n        \"output\": \" -2.29\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Bromoacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 1,2,3,4-Tetrachlorobenzene\\n\",\n        \"output\": \" 2.691534803926914e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2\\n\",\n        \"output\": \" 2.344228815319923e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCCCCCO\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Isopropyltoluene\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)NC(=O)N1CC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2\\n\",\n        \"output\": \" Rovral\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Octane\\n\",\n        \"output\": \" InChI=1S/C8H18/c1-3-5-7-8-6-4-2/h3-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1(C)C2CCC1(C)C(O)C2\\n\",\n        \"output\": \" borneol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-Hydroxybenzaldehyde \\n\",\n        \"output\": \" Oc1ccc(C=O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" phthalamide\\n\",\n        \"output\": \" [C][=C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][#Branch1][C][=C][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H9Cl/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H\\n\",\n        \"output\": \" -4.54\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H\\n\",\n        \"output\": \" 0.011748975549395297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC=C)c1ccccc1\\n\",\n        \"output\": \" 5-Allyl-5-phenylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 3,5-Dimethylpyridine\\n\",\n        \"output\": \" [C][C][=C][N][=C][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" o-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3\\n\",\n        \"output\": \" 0.008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)5(9)2-3/h1-2H\\n\",\n        \"output\": \" -4.63\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Atrazine\\n\",\n        \"output\": \" InChI=1S/C8H14ClN5/c1-4-10-7-12-6(9)13-8(14-7)11-5(2)3/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 0.10471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" p-Nitroanisole\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 5-Nonanone\\n\",\n        \"output\": \" InChI=1S/C9H18O/c1-3-5-7-9(10)8-6-4-2/h3-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-8-15-13(5-1)11-12-17-16-9-3-6-14-7-4-10-18(19(14)16)20(15)17/h1-12H\\n\",\n        \"output\": \" -8.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Hydrocortisone 21-acetate\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CCSC(=O)N(CC(C)C)CC(C)C\\n\",\n        \"output\": \" -3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H9ClF3N3O/c1-17-9-6-18-19(11(20)10(9)13)8-4-2-3-7(5-8)12(14,15)16/h2-6,17H,1H3\\n\",\n        \"output\": \" -4.046\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H7Br/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\\n\",\n        \"output\": \" 2-Bromotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0008260379495771783 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][O][C][Ring1][Branch1]\\n\",\n        \"output\": \" Tetrahydrofurane \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Hexanoyloxymethylphenyltoin\\n\",\n        \"output\": \" InChI=1S/C22H24N2O4/c1-2-3-6-15-19(25)28-16-24-20(26)22(23-21(24)27,17-11-7-4-8-12-17)18-13-9-5-10-14-18/h4-5,7-14H,2-3,6,15-16H2,1H3,(H,23,27)\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Diazepam\\n\",\n        \"output\": \" InChI=1S/C16H13ClN2O/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 2,2',3,4,5,5'-PCB\\n\",\n        \"output\": \" -7.68\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 7-methoxypteridine\\n\",\n        \"output\": \" -0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Carvacrol\\n\",\n        \"output\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][=C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(CC)Oc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" Trichloronate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 5-Allyl-5-ethylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O]\\n\",\n        \"output\": \" Lactose\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H18N2O4/c1-2-16(22)25-13-21-17(23)19(20-18(21)24,14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-12H,2,13H2,1H3,(H,20,24)\\n\",\n        \"output\": \" -4.907\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][N][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][P][O]\\n\",\n        \"output\": \" Salicin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2\\n\",\n        \"output\": \" 1,5-Hexadiene \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCN(CC)c1nc(Cl)nc(NC(C)C)n1\\n\",\n        \"output\": \" 0.00016405897731995388 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H6Cl4/c13-9-5-1-3-7(11(9)15)8-4-2-6-10(14)12(8)16/h1-6H\\n\",\n        \"output\": \" -7.28\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C3H4/c1-3-2/h1H,2H3\\n\",\n        \"output\": \" Propyne\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Heptyne\\n\",\n        \"output\": \" [C][C][C][C][C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.62\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H\\n\",\n        \"output\": \" hydrobenzoin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Ethylhexanal\\n\",\n        \"output\": \" -2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Coumachlor\\n\",\n        \"output\": \" CC(=O)CC(c1ccc(Cl)cc1)c2c(O)c3ccccc3oc2=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C21H30O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h11,15-18,22H,3-10,12H2,1-2H3\\n\",\n        \"output\": \" -3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Methyl propionate\\n\",\n        \"output\": \" -0.14\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Ethanoyloxymethylphenytoin\\n\",\n        \"output\": \" [O][=C][N][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 1,3-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-4(2)5(3)6/h4-6H,1-3H3\\n\",\n        \"output\": \" 3-Methyl-2-butanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 0.003235936569296281 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CN(C)C(=O)Nc1cccc(c1)C(F)(F)F\\n\",\n        \"output\": \" -3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCOCCCC\\n\",\n        \"output\": \" Dibutyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H3Cl3/c1-2(3,4)5/h1H3\\n\",\n        \"output\": \" 1,1,1-Trichloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,3,5-Trichlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Ethalfluralin\\n\",\n        \"output\": \" 7.516228940182061e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Fluvalinate\\n\",\n        \"output\": \" CC(C)C(Nc1ccc(cc1Cl)C(F)(F)F)C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Benomyl\\n\",\n        \"output\": \" InChI=1S/C14H18N4O3/c1-3-4-9-15-13(19)18-11-8-6-5-7-10(11)16-12(18)17-14(20)21-2/h5-8H,3-4,9H2,1-2H3,(H,15,19)(H,16,17,20)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCc1cccc2ccccc12\\n\",\n        \"output\": \" 1-Ethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H16ClO5PS/c1-4-17-21(22,18-5-2)20-10-6-7-12-11(8-10)9(3)13(15)14(16)19-12/h6-8H,4-5H2,1-3H3\\n\",\n        \"output\": \" -5.382000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Lenacil\\n\",\n        \"output\": \" -4.593999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Iodobenzene\\n\",\n        \"output\": \" 0.000977237220955811 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlorthalidone\\n\",\n        \"output\": \" NS(=O)(=O)c1cc(ccc1Cl)C2(O)NC(=O)c3ccccc23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCC(C)(C)O\\n\",\n        \"output\": \" 0.08317637711026708 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-isoPrbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Salicin\\n\",\n        \"output\": \" [O][C][C][O][C][Branch1][N][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][P][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][N][Branch1][#C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring1][=C][=O]\\n\",\n        \"output\": \" Methazole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Branch2][Ring1][#C][C][O][C][=Branch1][C][=O][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][#Branch2][Branch1][C][C][C][C][Branch1][C][F][=C][Ring2][Ring1][=Branch2][F]\\n\",\n        \"output\": \" Tetrafluthrin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Flumethasone\\n\",\n        \"output\": \" InChI=1S/C22H28F2O5/c1-11-6-13-14-8-16(23)15-7-12(26)4-5-19(15,2)21(14,24)17(27)9-20(13,3)22(11,29)18(28)10-25/h4-5,7,11,13-14,16-17,25,27,29H,6,8-10H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCC\\n\",\n        \"output\": \" 3.981071705534969e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1CCCO1\\n\",\n        \"output\": \" 2-Methyltetrahydrofurane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O]\\n\",\n        \"output\": \" d-inositol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Ethanoyloxymethylphenytoin\\n\",\n        \"output\": \" O=C1N(COC(=O)C)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2\\n\",\n        \"output\": \" 0.3890451449942806 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][O][Ring1][Branch1]\\n\",\n        \"output\": \" 2-Methyltetrahydrofurane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-5-7(3,4)6-2/h5-6H2,1-4H3\\n\",\n        \"output\": \" -4.23\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyclohexyl-5-spirobarbituric acid\\n\",\n        \"output\": \" InChI=1S/C9H12N2O3/c12-6-9(4-2-1-3-5-9)7(13)11-8(14)10-6/h1-5H2,(H2,10,11,12,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,3,4,6-Tetrachlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H2Cl4O/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2-Ethyl-2-hexanal\\n\",\n        \"output\": \" -2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Progesterone\\n\",\n        \"output\": \" 3.8018939632056124e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Ring1][Ring1][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][Branch2][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Procymidone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)N(C(C)C)C(=O)SCC(=CCl)Cl\\n\",\n        \"output\": \" -4.2860000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1nccc(C(=O)NN)c1\\n\",\n        \"output\": \" Isonazid\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cyclohexanol \\n\",\n        \"output\": \" -0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" Trifluralin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,4,6-Trinitrotoluene\\n\",\n        \"output\": \" Cc1c(cc(cc1N(=O)=O)N(=O)=O)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COP(=S)(OC)SCC(=O)N(C)C=O\\n\",\n        \"output\": \" Formothion\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][I][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" Iodofenphos\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCC(C(CC)c1ccc(O)cc1)c2ccc(O)cc2\\n\",\n        \"output\": \" 3.715352290971728e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][C][=Branch1][=N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 6.918309709189363e-10 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" m-Methylaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Branch1][C][O][Branch1][=Branch1][C][=Branch1][C][=O][C][C][Ring1][=Branch2][Branch1][C][C][C][C][Branch1][C][O][C][Ring1][#C][Branch1][C][F][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2]\\n\",\n        \"output\": \" 7.961593504173184e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h1H,4-6H2,2H3\\n\",\n        \"output\": \" 1-Hexyne \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C4H9Br/c1-4(2)3-5/h4H,3H2,1-2H3\\n\",\n        \"output\": \" 0.003715352290971724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)\\n\",\n        \"output\": \" -1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1cc(O)c(O)c2OCC3(O)CC4=CC(=O)C(O)=CC4=C3c21\\n\",\n        \"output\": \" 0.001995262314968879 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Biphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCSc1ccc(Cl)cc1\\n\",\n        \"output\": \" Carbophenthion\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Isopropalin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Atrazine\\n\",\n        \"output\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][#N]\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Furane\\n\",\n        \"output\": \" c1ccoc1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Diphenyl ether \\n\",\n        \"output\": \" 0.00010964781961431851 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility of given compound in room temperature. ->\",\n        \"input\": \" Terbutryn\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)n2cncn2\\n\",\n        \"output\": \" -3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Trichlorfon\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCBr\\n\",\n        \"output\": \" 1-Bromopentane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(=O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C\\n\",\n        \"output\": \" Progesterone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][N][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.21527817347243727 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc(O)c(C)c1\\n\",\n        \"output\": \" 2,4-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" Benzocaine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C2Cl3N/c3-2(4,5)1-6\\n\",\n        \"output\": \" Trichloroacetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 4-Methyl-2-pentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-5(2)4-6(3)7/h5-7H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Ethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Cc2cnc1cncnc1n2\\n\",\n        \"output\": \" -0.8540000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Dipropyl ether\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-3-5-7-6-4-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" p-Xylene \\n\",\n        \"output\": \" -2.77\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4/c7-3-1-2-4(8)6(10)5(3)9/h1-2H\\n\",\n        \"output\": \" 1,2,3,4-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" -2.616\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC(C)OP(=S)(OC(C)C)SCCNS(=O)(=O)c1ccccc1\\n\",\n        \"output\": \" -4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C\\n\",\n        \"output\": \" Ethofumesate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Octanol\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H16/c1-13-14(2)20-17-9-4-3-7-15(17)11-12-19(20)18-10-6-5-8-16(13)18/h3-12H,1-2H3\\n\",\n        \"output\": \" 5,6-Dimethylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C][O][C][=N][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" Benzoxazole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 1,1,2-Trichlorotrifluoroethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Hydrocortisone \\n\",\n        \"output\": \" CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1(O)C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)c2cc(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" 2.0892961308540408e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1c2ccccc2c(C)c3ccccc13\\n\",\n        \"output\": \" 9,10-Dimethylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\\n\",\n        \"output\": \" 0.007943282347242814 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H4N2/c1-2-5-4-6-3-1/h1-4H\\n\",\n        \"output\": \" 12.589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H16N2O3/c14-8-11(9(15)13-10(16)12-8)6-4-2-1-3-5-7-11/h1-7H2,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" Cyclooctyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2/c7-5-3-1-2-4-6(5)8/h1-4H\\n\",\n        \"output\": \" 1,2-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H7Br/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\\n\",\n        \"output\": \" -3.19\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Menthone\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][Ring1][#Branch1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [N][C][C][=N][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Ring1][=N][Cl]\\n\",\n        \"output\": \" 0.0013243415351946643 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-7-5-9(3)10(4)6-8(7)2/h5-6H,1-4H3\\n\",\n        \"output\": \" 1,2,4,5-Tetramethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H4ClI/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" -3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1cccc(O)c1\\n\",\n        \"output\": \" 3-Methylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" o-Toluidine\\n\",\n        \"output\": \" Cc1ccccc1N\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][C][Branch1][C][C][O][C][C]\\n\",\n        \"output\": \" 0.37153522909717257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H38O4/c1-19(2)13-7-5-11-17-27-23(25)21-15-9-10-16-22(21)24(26)28-18-12-6-8-14-20(3)4/h9-10,15-16,19-20H,5-8,11-14,17-18H2,1-4H3\\n\",\n        \"output\": \" diisooctyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" o-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][NH1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=Branch1][C][=O][C][=Ring1][Branch2][Cl][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.484\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-terphenyl\\n\",\n        \"output\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2,3',4',5-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H16ClN5/c1-5(2)11-8-13-7(10)14-9(15-8)12-6(3)4/h5-6H,1-4H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" Propazine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Coumaphos\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][O][C][=Branch1][C][=O][C][Branch1][C][Cl][=C][Branch1][C][C][C][Ring1][=Branch2][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,3,5,6-Tetrachlorophenol\\n\",\n        \"output\": \" [O][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC(C)(C)CO\\n\",\n        \"output\": \" 2,2-Dimethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"What is oil solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C5H10/c1-3-5-4-2/h3H,1,4-5H2,2H3\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CI\\n\",\n        \"output\": \" Iodomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H\\n\",\n        \"output\": \" 1,3-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H19N3O/c1-4-6-7-9-8(3)13-11(12-5-2)14-10(9)15/h4-7H2,1-3H3,(H2,12,13,14,15)\\n\",\n        \"output\": \" Ethirimol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1cccc(c1)N(=O)=O\\n\",\n        \"output\": \" m-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Bromochloromethane\\n\",\n        \"output\": \" [Cl][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccccc1N(=O)=O\\n\",\n        \"output\": \" o-Nitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(O)CC\\n\",\n        \"output\": \" 3-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Ethyl octanoate\\n\",\n        \"output\": \" -3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)Cl\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-6(2)3-4-8-5-7/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" Isopentyl formate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-Nitroaniline\\n\",\n        \"output\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethyne\\n\",\n        \"output\": \" InChI=1S/C2H2/c1-2/h1-2H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H22N2O/c1-13(2)11(14)12-10-8-6-4-3-5-7-9-10/h10H,3-9H2,1-2H3,(H,12,14)\\n\",\n        \"output\": \" Cycluron\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" ClCCCCl\\n\",\n        \"output\": \" 0.023988329190194897 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][=C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.0025703957827688645 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H6ClN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2\\n\",\n        \"output\": \" -1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3,5-Dichlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1[nH]c(=O)n(c(=O)c1Cl)C(C)(C)C\\n\",\n        \"output\": \" Terbacil\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC#N\\n\",\n        \"output\": \" Acetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.18197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)Br\\n\",\n        \"output\": \" -1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Napthalene\\n\",\n        \"output\": \" -3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][Branch1][C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][Branch1][C][C][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Methoprene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H14/c1-2-7-16-13(4-1)8-10-17-18-11-9-14-5-3-6-15(20(14)18)12-19(16)17/h1-8,10,12H,9,11H2\\n\",\n        \"output\": \" Cholanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCC(=O)OC\\n\",\n        \"output\": \" Propyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][C][Br][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][Branch1][C][N][=O]\\n\",\n        \"output\": \" Carbromal\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,2-Dimethylpropanol\\n\",\n        \"output\": \" 0.3981071705534972 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\\n\",\n        \"output\": \" Dinitramine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" -2.89\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 5-Allyl-5-methylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(C)CC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][O][C][C][O]\\n\",\n        \"output\": \" 2-Butoxyethanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7-\\n\",\n        \"output\": \" Nerol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" benzhydrol\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Perfluidone\\n\",\n        \"output\": \" InChI=1S/C14H12F3NO4S2/c1-10-9-12(23(19,20)11-5-3-2-4-6-11)7-8-13(10)18-24(21,22)14(15,16)17/h2-9,18H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCNc1nc(NC(C)(C)C)nc(SC)n1\\n\",\n        \"output\": \" Terbutryn\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" ethofumesate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" benzhydrol\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccccc1N(=O)=O\\n\",\n        \"output\": \" o-Chloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3\\n\",\n        \"output\": \" 0.00011091748152624009 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" methylthiouracil\\n\",\n        \"output\": \" Cc1cc(=O)[nH]c(=S)[nH]1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-8-16-15(7-1)17-9-3-5-13-11-12-14-6-4-10-18(16)20(14)19(13)17/h1-12H\\n\",\n        \"output\": \" Benzo(e)pyrene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C21H30O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h12,16-18,24H,4-11H2,1-3H3\\n\",\n        \"output\": \" -3.8169999999999997\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCC(C)O\\n\",\n        \"output\": \" 0.028183829312644536 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Tetrahydropyran \\n\",\n        \"output\": \" 0.933254300796991 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H11ClN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\\n\",\n        \"output\": \" -2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" -5.233\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][=C][C][N][C][=C][N][=C][Ring1][Branch1][N][=Branch1][C][=O][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benznidazole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H12Cl3O2PS/c1-3-14-16(17,4-2)15-10-6-8(12)7(11)5-9(10)13/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" Trichloronate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2Cl3F3/c3-1(4,6)2(5,7)8\\n\",\n        \"output\": \" 1,1,2-Trichlorotrifluoroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Propylisopropylether\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" Amobarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][#C]\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 4-Methylpentanol\\n\",\n        \"output\": \" 0.07244359600749903 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][Ring1][C][#N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][Ring1][=N]\\n\",\n        \"output\": \" Chlorothalonil\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=N][C][=N][Ring1][Branch1]\\n\",\n        \"output\": \" 0.0002454708915685031 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Trichloromethane\\n\",\n        \"output\": \" ClC(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCN(=O)=O\\n\",\n        \"output\": \" 1-Nitropropane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H5NO3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H\\n\",\n        \"output\": \" o-Nitrophenol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc2cnccc2c1\\n\",\n        \"output\": \" Isoquinoline\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc(cc1)c2ccccc2\\n\",\n        \"output\": \" 4.518559443749226e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 1-Octanol\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][=C][Branch1][S][C][=Branch1][C][=O][O][C][C][C][C][C][C][Branch1][C][C][C][C][=C][C][=C][Ring2][Ring1][N]\\n\",\n        \"output\": \" -6.6370000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H4BrCl/c3-1-2-4/h1-2H2\\n\",\n        \"output\": \" 0.047863009232263824 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C24H28N2O4/c1-2-3-4-5-12-17-21(27)30-18-26-22(28)24(25-23(26)29,19-13-8-6-9-14-19)20-15-10-7-11-16-20/h6-11,13-16H,2-5,12,17-18H2,1H3,(H,25,29)\\n\",\n        \"output\": \" 2.9991625189876533e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CN(C)C(=O)C\\n\",\n        \"output\": \" 12.882495516931343 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Reposal\\n\",\n        \"output\": \" [C][C][C][Branch1][#C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][Branch2][=O][C][=C][C][C][C][C][C][Ring1][#Branch1][C][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H13N3O2/c1-9-7-11(15-17-9)12(16)14-13-8-10-5-3-2-4-6-10/h2-7,13H,8H2,1H3,(H,14,16)\\n\",\n        \"output\": \" Isocarboxazid\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" 0.23988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3\\n\",\n        \"output\": \" 1.4125375446227544 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,1-Dichloroethylene\\n\",\n        \"output\": \" ClC(=C)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C9H12N2O2/c1-2-13-8-5-3-7(4-6-8)11-9(10)12/h3-6H,2H2,1H3,(H3,10,11,12)\\n\",\n        \"output\": \" 0.006760829753919818 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C]\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(C)(C)c1ccccc1\\n\",\n        \"output\": \" 0.00021877616239495518 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Isocarboxazid\\n\",\n        \"output\": \" [C][C][=C][C][=Branch1][Branch1][=N][O][Ring1][Branch1][C][=Branch1][C][=O][N][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Trichlorfon\\n\",\n        \"output\": \" InChI=1S/C4H8Cl3O4P/c1-10-12(9,11-2)3(8)4(5,6)7/h3,8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H14ClN3OS/c1-3-14(4-2)10(15)7-16-9-6-5-8(11)12-13-9/h5-6H,3-4,7H2,1-2H3\\n\",\n        \"output\": \" Azintamide\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 7-methylpteridine\\n\",\n        \"output\": \" InChI=1S/C7H6N4/c1-5-2-9-6-3-8-4-10-7(6)11-5/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Propanol\\n\",\n        \"output\": \" CC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][Ring2][=C][Ring1][=N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" Fluridone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3\\n\",\n        \"output\": \" 2-Ethyl pyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" love\\n\",\n        \"output\": \" love does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CSC\\n\",\n        \"output\": \" -0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Cyhalothrin\\n\",\n        \"output\": \" -8.176\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Isopropalin\\n\",\n        \"output\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][C][C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C4Cl6/c5-1(3(7)8)2(6)4(9)10\\n\",\n        \"output\": \" 1.2022644346174132e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCC\\n\",\n        \"output\": \" -5.88\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C]\\n\",\n        \"output\": \" Methyl acrylate\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,5-Hexadiene \\n\",\n        \"output\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][/C][=C][/C]\\n\",\n        \"output\": \" trans-2-Heptene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propylene\\n\",\n        \"output\": \" CC=C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H18O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h2-5,10,16,19H,6-9H2,1H3\\n\",\n        \"output\": \" Equilenin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1cc2c3ccccc3ccc2c4ccccc14\\n\",\n        \"output\": \" -6.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][=C][Branch1][C][O][C][C][=Branch1][C][=O][C][C][=C][Branch1][C][O][C][=C][C][Ring1][#Branch1][O][C][Ring1][N][C][=C][Ring1][P][O][C]\\n\",\n        \"output\": \" -2.943\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOP(=O)(OCC)OCC\\n\",\n        \"output\": \" Triethyl phosphate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Cl)CC(=O)NC2=C(Cl)C(=O)c1ccccc1C2=O\\n\",\n        \"output\": \" Quinonamid\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1ccc2c(c1)c3ccccc3c4ccccc24\\n\",\n        \"output\": \" 1.8793168168032686e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 5-Allyl-5-methylbarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 2,3,4,6-Tetrachlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-5(2,3)4-6/h6H,4H2,1-3H3\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3-Chlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)\\n\",\n        \"output\": \" Triamterene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H6/c1-3-4-2/h1H,4H2,2H3\\n\",\n        \"output\": \" -1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCC=C\\n\",\n        \"output\": \" 0.01148153621496883 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" 0.14791083881682077 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethirimol\\n\",\n        \"output\": \" CCCCc1c(C)nc(NCC)[nH]c1=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Acetamide\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" -1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCNc1nc(Cl)nc(n1)N(CC)CC\\n\",\n        \"output\": \" -4.06\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Prasterone\\n\",\n        \"output\": \" -4.12\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H6N4O/c1-12-6-3-9-7-5(11-6)2-8-4-10-7/h2-4H,1H3\\n\",\n        \"output\": \" -1.139\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CSc1nc(nc(n1)N(C)C)N(C)C\\n\",\n        \"output\": \" Simetryn\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 3-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch1][C][=C][Ring1][Branch1][C][Ring1][#Branch1][C][Ring1][=N][Branch1][C][Cl][C][Ring1][N][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -6.307\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(SC)c(C)c1\\n\",\n        \"output\": \" 2.691534803926914e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Primidone\\n\",\n        \"output\": \" CCC1(C(=O)NCNC1=O)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H12Cl3O2PS/c1-3-14-16(17,4-2)15-10-6-8(12)7(11)5-9(10)13/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" -5.752000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" o-Nitrophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" COP(=O)(OC)OC(Br)C(Cl)(Cl)Br\\n\",\n        \"output\": \" -2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Chlorobutane\\n\",\n        \"output\": \" CCC(C)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" p-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-10(2,3)9-7-5-4-6-8-9/h4-8H,1-3H3\\n\",\n        \"output\": \" -3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dihexyl phthalate\\n\",\n        \"output\": \" InChI=1S/C20H30O4/c1-3-5-7-11-15-23-19(21)17-13-9-10-14-18(17)20(22)24-16-12-8-6-4-2/h9-10,13-14H,3-8,11-12,15-16H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Nitrofen\\n\",\n        \"output\": \" Clc2ccc(Oc1ccc(cc1)N(=O)=O)c(Cl)c2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Cl)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" Pentachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" DEF\\n\",\n        \"output\": \" CCCCSP(=O)(SCCCC)SCCCC\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" N,N-Diethylaniline\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Terbutryn\\n\",\n        \"output\": \" InChI=1S/C10H19N5S/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][#C]\\n\",\n        \"output\": \" 1-Hexyne \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)\\n\",\n        \"output\": \" -1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(C)c(Cl)c1\\n\",\n        \"output\": \" 0.000328851630875983 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Chloro-2-methylbutane\\n\",\n        \"output\": \" 0.003090295432513592 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dialifos\\n\",\n        \"output\": \" InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COC(=O)Nc2nc1ccc(cc1[nH]2)C(=O)c3ccccc3\\n\",\n        \"output\": \" Mebendazole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ccc(Br)cc1\\n\",\n        \"output\": \" 4-Bromotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Isopropyl formate\\n\",\n        \"output\": \" CC(C)OC=O\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][=C][O][P][=Branch1][C][=O][Branch1][=N][O][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 9.77237220955811e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methyl-2-hexanol\\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-4-5-6-7(2,3)8/h8H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H12N2O3/c1-2-8-13(9-6-4-3-5-7-9)10(16)14-12(18)15-11(13)17/h2-7H,1,8H2,(H2,14,15,16,17,18)\\n\",\n        \"output\": \" 5-Allyl-5-phenylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][#Branch1][S][C][C][O][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Carboxin\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCOC\\n\",\n        \"output\": \" 0.40738027780411273 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" OCC2OC(Oc1ccccc1CO)C(O)C(O)C2O\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 8.91250938133746e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCC1COC(Cn2cncn2)(O1)c3ccc(Cl)cc3Cl\\n\",\n        \"output\": \" 0.00032136605386403147 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/CH2I2/c2-1-3/h1H2\\n\",\n        \"output\": \" -2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CH4O/c1-2/h2H,1H3\\n\",\n        \"output\": \" Methanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Styrene\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][N][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 2.3988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" Cycloheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC34CCc1c(ccc2cc(O)ccc12)C3CCC4=O\\n\",\n        \"output\": \" -5.24\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H10O3/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCN(CC)c1nc(Cl)nc(n1)N(CC)CC\\n\",\n        \"output\": \" Chlorazine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H9Cl2NO/c1-2-9(13)12-6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3,(H,12,13)\\n\",\n        \"output\": \" Propanil\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Carbazole\\n\",\n        \"output\": \" c1ccc2c(c1)[nH]c3ccccc32\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C][=C]\\n\",\n        \"output\": \" 0.009332543007969915 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,2,3-Trimethylbutane\\n\",\n        \"output\": \" InChI=1S/C7H16/c1-6(2)7(3,4)5/h6H,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methaqualone\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" Estrone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC12CCC(O)CC1CCC3C2CCC4(C)C3CCC4=O\\n\",\n        \"output\": \" Androsterone\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Metribuzin\\n\",\n        \"output\": \" InChI=1S/C8H14N4OS/c1-8(2,3)5-6(13)12(9)7(14-4)11-10-5/h9H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][Branch1][C][C][C][C][C][C][C][=C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][C][C][C][Ring2][Ring1][Branch1][Ring1][P][C]\\n\",\n        \"output\": \" -5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-4-6-7-8(3,9)5-2/h9H,4-7H2,1-3H3\\n\",\n        \"output\": \" 3-Methyl-3-heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12/c1-4-5-6(2)3/h2,4-5H2,1,3H3\\n\",\n        \"output\": \" 0.0009332543007969915 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][P][Ring1][#Branch2]\\n\",\n        \"output\": \" Benzo(a)fluorene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2,3,4-Tetrahydronapthalene\\n\",\n        \"output\": \" [C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H4F2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Cyanazine\\n\",\n        \"output\": \" 0.000707945784384138 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CSC\\n\",\n        \"output\": \" Dimethyl sulfide\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Niclosamide\\n\",\n        \"output\": \" Oc1ccc(Cl)cc1C(=O)Nc2ccc(cc2Cl)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Phenanthrene\\n\",\n        \"output\": \" c1ccc2c(c1)ccc3ccccc32\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" Diuron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H9Cl2NO2/c12-6-1-2-7-16-11(15)14-10-5-3-4-9(13)8-10/h3-5,8H,6-7H2,(H,14,15)\\n\",\n        \"output\": \" Barban\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cccc(I)c1\\n\",\n        \"output\": \" m-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C3H6O/c1-2-3-4/h3H,2H2,1H3\\n\",\n        \"output\": \" Propionaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)SC(CCl)N2C(=O)c1ccccc1C2=O\\n\",\n        \"output\": \" Dialifos\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H18N2O3/c1-7(2)5-6-12(8(3)4)9(15)13-11(17)14-10(12)16/h5,8H,6H2,1-4H3,(H2,13,14,15,16,17)\\n\",\n        \"output\": \" 5-(3-Methyl-2-butenyl)-5-isoPrbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Glycerol\\n\",\n        \"output\": \" 13.182567385564074 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Dinitramine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=Branch1][=C][=C][Branch1][C][Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl][Cl]\\n\",\n        \"output\": \" Hexachloro-1,3-butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-3-5-6(7)8-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" 0.043651583224016584 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Iodomethane\\n\",\n        \"output\": \" CI\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-2-10-7-5-8-11-6-3-4-9-12(10)11/h3-9H,2H2,1H3\\n\",\n        \"output\": \" 1-Ethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Terbumeton\\n\",\n        \"output\": \" CCNc1nc(NC(C)(C)C)nc(OC)n1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" -4.29\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" oryzalin\\n\",\n        \"output\": \" InChI=1S/C12H18N4O6S/c1-3-5-14(6-4-2)12-10(15(17)18)7-9(23(13,21)22)8-11(12)16(19)20/h7-8H,3-6H2,1-2H3,(H2,13,21,22)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Chlorodibromethane\\n\",\n        \"output\": \" InChI=1S/CHBr2Cl/c2-1(3)4/h1H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C\\n\",\n        \"output\": \" -3.8169999999999997\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-5-7(8)9-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" Ethyl pentanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 4-Methyl-2-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-5-7-6(2)3/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 6-Methylchrysene\\n\",\n        \"output\": \" Cc1cc2c3ccccc3ccc2c4ccccc14\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Fluorene \\n\",\n        \"output\": \" C1c2ccccc2c3ccccc13\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1,3,5-Trimethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Bromobutane\\n\",\n        \"output\": \" InChI=1S/C4H9Br/c1-2-3-4-5/h2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" C1=Cc2cccc3cccc1c23\\n\",\n        \"output\": \" -3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Acenapthene\\n\",\n        \"output\": \" InChI=1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc(cc1)c2ccccc2\\n\",\n        \"output\": \" Biphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Riboflavin\\n\",\n        \"output\": \" -3.685\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Pebulate\\n\",\n        \"output\": \" [C][C][C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][S][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Oxadiazon\\n\",\n        \"output\": \" CC(C)Oc1cc(c(Cl)cc1Cl)n2nc(oc2=O)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Valeraldehyde\\n\",\n        \"output\": \" CCCCC=O\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 1,2,3,5-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Hexene-3-ol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][O][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Cc1cc(C)cc(C)c1\\n\",\n        \"output\": \" 0.00039810717055349735 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H\\n\",\n        \"output\": \" 0.005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1cccc(O)c1\\n\",\n        \"output\": \" 0.20892961308540392 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCC(=O)OC\\n\",\n        \"output\": \" Propyl propanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3\\n\",\n        \"output\": \" 1-Hexadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCC(=O)OC3(C(C)CC4C2CCC1=CC(=O)C=CC1(C)C2(F)C(O)CC34C)C(=O)CO\\n\",\n        \"output\": \" Betamethasone-17-valerate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" c2ccc1ocnc1c2\\n\",\n        \"output\": \" -1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Butamben\\n\",\n        \"output\": \" [C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Brc1ccc(Br)cc1\\n\",\n        \"output\": \" 8.51138038202376e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Chlorohexane\\n\",\n        \"output\": \" InChI=1S/C6H13Cl/c1-2-3-4-5-6-7/h2-6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Diethyldisulfide\\n\",\n        \"output\": \" CCSSCC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H\\n\",\n        \"output\": \" 2,3-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Amobarbital\\n\",\n        \"output\": \" InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2\\n\",\n        \"output\": \" 1-Napthylamine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\\n\",\n        \"output\": \" Endrin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCC(C)(O)CC\\n\",\n        \"output\": \" 3-Methyl-3-heptanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Corticosterone\\n\",\n        \"output\": \" 0.0005754399373371566 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" DDD\\n\",\n        \"output\": \" ClC(Cl)C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 5,5-Dimethylbarbituric acid\\n\",\n        \"output\": \" -1.742\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC(C)OCC\\n\",\n        \"output\": \" 1,1-Diethoxyethane \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][Branch1][C][O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Buthidazole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methyl propyl ether \\n\",\n        \"output\": \" CCCOC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1(C)C2CCC1(C)C(=O)C2\\n\",\n        \"output\": \" Camphor\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dialifos\\n\",\n        \"output\": \" CCOP(=S)(OCC)SC(CCl)N2C(=O)c1ccccc1C2=O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)c1ccccc1\\n\",\n        \"output\": \" -2.322\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methylpropan-1-ol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.003890451449942805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzonitrile\\n\",\n        \"output\": \" N#Cc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.1318256738556407 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H\\n\",\n        \"output\": \" Benzonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5-Methylchrysene\\n\",\n        \"output\": \" InChI=1S/C19H14/c1-13-12-15-7-3-4-8-16(15)18-11-10-14-6-2-5-9-17(14)19(13)18/h2-12H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" p-terphenyl\\n\",\n        \"output\": \" 7.762471166286912e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H3N/c1-2-3/h1H3\\n\",\n        \"output\": \" Acetonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Nc3nc(N)c2nc(c1ccccc1)c(N)nc2n3\\n\",\n        \"output\": \" Triamterene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccc(Br)cc1\\n\",\n        \"output\": \" 4-Bromophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H6N2O2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H,7H2\\n\",\n        \"output\": \" m-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" alloxantin\\n\",\n        \"output\": \" 0.010232929922807542 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1cccc2c(C)cccc12\\n\",\n        \"output\": \" -4.678999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClCCCCl\\n\",\n        \"output\": \" 1,3-Dichloropropane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Eicosane\\n\",\n        \"output\": \" InChI=1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Iodonapthalene\\n\",\n        \"output\": \" Ic1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Chlorobutane\\n\",\n        \"output\": \" InChI=1S/C4H9Cl/c1-3-4(2)5/h4H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][C][C][C][C]\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H19ClO3/c23-16-11-9-14(10-12-16)13-5-7-15(8-6-13)19-20(24)17-3-1-2-4-18(17)21(25)22(19)26/h1-4,9-13,15,26H,5-8H2\\n\",\n        \"output\": \" Atovaquone(0,430mg/ml) - neutral\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Pyrene\\n\",\n        \"output\": \" c1cc2ccc3cccc4ccc(c1)c2c34\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCc1ccccc1\\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2\\n\",\n        \"output\": \" allicin\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC1CC2C3CCC(O)(C(=O)C)C3(C)CC(O)C2(F)C4(C)C=CC(=O)C=C14\\n\",\n        \"output\": \" 7.961593504173184e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][=C][C][=C][NH1][N][=N][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.16595869074375605 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H23N3/c1-14-6-8-18(16(3)10-14)20-12-22(5)13-21-19-9-7-15(2)11-17(19)4/h6-13H,1-5H3\\n\",\n        \"output\": \" Amitraz\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Ronnel\\n\",\n        \"output\": \" 1.9054607179632483e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)c1ccc(NC(=O)N(C)C)cc1\\n\",\n        \"output\": \" -3.536\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Reposal\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Chlorobutane\\n\",\n        \"output\": \" InChI=1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Tetradecane\\n\",\n        \"output\": \" 1.0964781961431851e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2-Octanone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H18/c1-4-6-7-8(3)5-2/h8H,4-7H2,1-3H3\\n\",\n        \"output\": \" 3-Methylheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][Branch1][C][O][C][C][=Branch1][C][=O][C][C][=C][Branch1][C][O][C][=C][C][Ring1][#Branch1][O][C][Ring1][N][C][=C][Ring1][P][O][C]\\n\",\n        \"output\": \" gentisin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,2',3,4,5,5',6-PCB\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1cc2ccccc2cc1C\\n\",\n        \"output\": \" 1.9054607179632484e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Clc1ccc(cc1)C(c2ccc(Cl)cc2)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" 7.079457843841373e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" o1c2ccccc2c3ccccc13\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][Cl][C][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" -2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" -1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC1C=CC2C1C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl\\n\",\n        \"output\": \" Heptachlor\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Fluridone\\n\",\n        \"output\": \" Cn2cc(c1ccccc1)c(=O)c(c2)c3cccc(c3)C(F)(F)F\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC1(C)C2CCC1(C)C(O)C2\\n\",\n        \"output\": \" -2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Dialifor\\n\",\n        \"output\": \" -6.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Toluene \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" norflurazon\\n\",\n        \"output\": \" -4.046\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1N(COC(=O)CCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3-Hexanoyloxymethylphenyltoin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Methylphenanthrene\\n\",\n        \"output\": \" InChI=1S/C15H12/c1-11-5-4-8-15-13(11)10-9-12-6-2-3-7-14(12)15/h2-10H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Cycluron\\n\",\n        \"output\": \" 0.006053408747539136 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][C][C]\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Diethyl sulfide\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCC(=O)CCC\\n\",\n        \"output\": \" 4-Heptanone\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C13H9N/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-9H\\n\",\n        \"output\": \" -3.67\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Bromopropane\\n\",\n        \"output\": \" CC(C)Br\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H18NO4PS2/c1-7(8(10)9-2)15-5-6-16-14(11,12-3)13-4/h7H,5-6H2,1-4H3,(H,9,10)\\n\",\n        \"output\": \" 1.1440000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Oxadiazon\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2,4-Dimethyl-2-pentanol \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Carbetamide\\n\",\n        \"output\": \" InChI=1S/C12H16N2O3/c1-3-13-11(15)9(2)17-12(16)14-10-7-5-4-6-8-10/h4-9H,3H2,1-2H3,(H,13,15)(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Chlorotoluene\\n\",\n        \"output\": \" InChI=1S/C7H7Cl/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][=Branch1][Ring1][=C][Cl][Cl]\\n\",\n        \"output\": \" Diallate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][/C][C][C][C][C][C][Ring1][=Branch1][\\\\C]\\n\",\n        \"output\": \" -4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H6N4O/c1-12-6-3-9-5-2-8-4-10-7(5)11-6/h2-4H,1H3\\n\",\n        \"output\": \" 0.12302687708123815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][S][C][=C][C][=C][Branch1][N][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][C][=C][Ring1][=N][C][=C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" Abate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Lactose\\n\",\n        \"output\": \" -0.244\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Malonic acid diethylester\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C11H16N2O3/c1-4-6-11(7(3)5-2)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" 0.009638290236239706 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" d-Limonene\\n\",\n        \"output\": \" CC1=CCC(CC1)C(C)=C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Carboxin\\n\",\n        \"output\": \" InChI=1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Phosalone\\n\",\n        \"output\": \" InChI=1S/C12H15ClNO4PS2/c1-3-16-19(20,17-4-2)21-8-14-10-6-5-9(13)7-11(10)18-12(14)15/h5-7H,3-4,8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COc1ccccc1N(=O)=O\\n\",\n        \"output\": \" o-Nitroanisole\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C22H18Cl2FNO3/c1-22(2)15(11-19(23)24)20(22)21(27)29-18(12-26)13-8-9-16(25)17(10-13)28-14-6-4-3-5-7-14/h3-11,15,18,20H,1-2H3\\n\",\n        \"output\": \" Cyfluthrin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)OC(C)C\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][Branch1][P][C][=Branch1][Ring1][=C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -4.95\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 4-Ethyltoluene\\n\",\n        \"output\": \" CCc1ccc(C)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Propanol\\n\",\n        \"output\": \" CCCO\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Butanone\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethyne\\n\",\n        \"output\": \" [C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methaqualone\\n\",\n        \"output\": \" Cc1ccccc1n3c(C)nc2ccccc2c3=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its solubility expressed as a logarithm in mol/L. ->\",\n        \"input\": \" 2-Bromonapthalene\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Succinimide\\n\",\n        \"output\": \" 1.9952623149688795 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" O=C1N(COC(=O)CCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 2.0989398836235246e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3/c7-4-1-5(8)3-6(9)2-4/h1-3H\\n\",\n        \"output\": \" 3.3113112148259076e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" m-Nitrotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccc2c(c1)c3cccc4cccc2c34\\n\",\n        \"output\": \" Fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Atovaquone(0,430mg/ml) - neutral\\n\",\n        \"output\": \" OC4=C(C1CCC(CC1)c2ccc(Cl)cc2)C(=O)c3ccccc3C4=O\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dexamethasone\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][C][Branch1][C][C][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H18/c1-3-5-7-8-6-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" Octane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(NC(C)C)Oc1ccccc1C(=O)OC(C)C\\n\",\n        \"output\": \" Isofenphos\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][NH1][C][C][C][C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][#Branch2][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Lenacil\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzo(b)fluorene\\n\",\n        \"output\": \" C1c2ccccc2c3cc4ccccc4cc13\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-1-5(8)3-6(9)2-4/h1-3,9H\\n\",\n        \"output\": \" 3,5-Dichlorophenol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Isopentyl formate\\n\",\n        \"output\": \" InChI=1S/C6H12O2/c1-6(2)3-4-8-5-7/h5-6H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ethane\\n\",\n        \"output\": \" InChI=1S/C2H6/c1-2/h1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COCCCNc1nc(NC(C)C)nc(SC)n1\\n\",\n        \"output\": \" Methoproptryne\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Methylphenol\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Chlortoluron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC12CCC3C(CCc4cc(O)ccc34)C2CCC1=O\\n\",\n        \"output\": \" Estrone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pebulate\\n\",\n        \"output\": \" CCCCN(CC)C(=O)SCCC\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H10/c1-7-3-5-8(2)6-4-7/h3-6H,1-2H3\\n\",\n        \"output\": \" p-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCC(C)(C)C\\n\",\n        \"output\": \" 0.0002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H13N3O3S/c1-8-7(12)13-9-5(14-4)6(11)10(2)3/h1-4H3,(H,8,12)\\n\",\n        \"output\": \" Oxamyl\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C17H20N4O6/c1-7-3-9-10(4-8(7)2)21(5-11(23)14(25)12(24)6-22)15-13(18-9)16(26)20-17(27)19-15/h3-4,11-12,14,22-25H,5-6H2,1-2H3,(H,20,26,27)\\n\",\n        \"output\": \" -3.685\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3\\n\",\n        \"output\": \" ethyl cinnamate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Propionaldehyde\\n\",\n        \"output\": \" CCC=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" FC(F)(Cl)C(F)(Cl)Cl\\n\",\n        \"output\": \" 1,1,2-Trichlorotrifluoroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 5-Methyl-5-ethylbarbituric acid\\n\",\n        \"output\": \" InChI=1S/C7H10N2O3/c1-3-7(2)4(10)8-6(12)9-5(7)11/h3H2,1-2H3,(H2,8,9,10,11,12)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-5(2,3)4-6/h6H,4H2,1-3H3\\n\",\n        \"output\": \" 2,2-Dimethylpropanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Benzo(a)fluorene\\n\",\n        \"output\": \" 2.0892961308540409e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOC(=O)c1cncn1C(C)c2ccccc2\\n\",\n        \"output\": \" Etomidate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" C1CCCCCCC1\\n\",\n        \"output\": \" -4.15\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][C][C][Branch1][C][C][C][C][C][C][C][Branch1][C][C][C][Branch1][C][C][C][C][O][C][C][Branch1][C][C][C][C][Ring1][#Branch1][O][C][Ring1][N][C][C][Ring1][S][C][Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=C]\\n\",\n        \"output\": \" -7.32\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Octyne \\n\",\n        \"output\": \" InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h1H,4-8H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Pentanone\\n\",\n        \"output\": \" [C][C][C][=Branch1][C][=O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Methylpropane\\n\",\n        \"output\": \" CC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility of given compound in room temperature. ->\",\n        \"input\": \" Thiourea\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Santonin\\n\",\n        \"output\": \" InChI=1S/C15H18O3/c1-8-10-4-6-15(3)7-5-11(16)9(2)12(15)13(10)18-14(8)17/h5,7-8,10,13H,4,6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" o-Methoxyphenol\\n\",\n        \"output\": \" COc1ccccc1O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Methyl hexanoate\\n\",\n        \"output\": \" -1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Pyrazinamide\\n\",\n        \"output\": \" InChI=1S/C5H5N3O/c6-5(9)4-3-7-1-2-8-4/h1-3H,(H2,6,9)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4Cl6/c5-1(3(7)8)2(6)4(9)10\\n\",\n        \"output\": \" Hexachloro-1,3-butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" m-Chloroiodobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][Branch1][C][I][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Pentylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=Branch1][C][=O][N][Ring1][O]\\n\",\n        \"output\": \" Cyclobutyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Br]\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" brompyrazone\\n\",\n        \"output\": \" c1ccccc1n2ncc(N)c(Br)c2(=O)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Nonyne \\n\",\n        \"output\": \" CCCCCCCC#C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,4-Pentadiene \\n\",\n        \"output\": \" InChI=1S/C5H8/c1-3-5-4-2/h3-4H,1-2,5H2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CO\\n\",\n        \"output\": \" Methanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=Branch1][=N][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 2,2',3,3',4,4',5,5'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-3-5-6-7(8)9-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" -2.25\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Diuron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1ccc(Cl)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" COP(=S)(OC)Oc1cc(Cl)c(Br)cc1Cl\\n\",\n        \"output\": \" -6.09\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Nc1ccc(cc1)c2ccc(N)cc2\\n\",\n        \"output\": \" 0.001995262314968879 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" COc1ccccc1OCC(O)COC(N)=O\\n\",\n        \"output\": \" 0.10351421666793438 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H2Cl8/c13-5-1-3(7(15)11(19)9(5)17)4-2-6(14)10(18)12(20)8(4)16/h1-2H\\n\",\n        \"output\": \" -9.16\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Methylcyclohexene \\n\",\n        \"output\": \" InChI=1S/C7H12/c1-7-5-3-2-4-6-7/h5H,2-4,6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.004764309868054156 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCn1c(=O)oc2cc(Cl)ccc12\\n\",\n        \"output\": \" Phosalone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H5N/c1-2-4-6-5-3-1/h1-5H\\n\",\n        \"output\": \" 5.7543993733715695 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Naled\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Branch1][C][Br][C][Branch1][C][Cl][Branch1][C][Cl][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-4-5-6(2)7/h3-5H2,1-2H3\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pentane\\n\",\n        \"output\": \" CCCCC\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Oxycarboxin\\n\",\n        \"output\": \" [C][C][=C][Branch1][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][O][Ring1][P]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Butene\\n\",\n        \"output\": \" InChI=1S/C4H8/c1-3-4-2/h3H,1,4H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Eicosane\\n\",\n        \"output\": \" CCCCCCCCCCCCCCCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cc(c(Cl)c(Cl)c1Cl)c2cc(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" 2,2',3,3',4,4',5,5'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Methyl benzoate \\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write oil solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CC1=C(SCCO1)C(=O)Nc2ccccc2\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Etomidate\\n\",\n        \"output\": \" CCOC(=O)c1cncn1C(C)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Disulfoton\\n\",\n        \"output\": \" CCOP(=S)(OCC)SCCSCC\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][O][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" 6.668067692136219e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)Oc1nc(nc(C)c1C)N(C)C\\n\",\n        \"output\": \" Pirimicarb\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3\\n\",\n        \"output\": \" Methylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Methyl-1-Pentene\\n\",\n        \"output\": \" InChI=1S/C6H12/c1-4-5-6(2)3/h2,4-5H2,1,3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCC=C\\n\",\n        \"output\": \" 1-Pentene \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" o-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Chloro-2-methylpropane\\n\",\n        \"output\": \" InChI=1S/C4H9Cl/c1-4(2)3-5/h4H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" N#Cc1ccccc1C#N\\n\",\n        \"output\": \" Phthalonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 5-Methyl-5-ethylbarbituric acid\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanone\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Butene\\n\",\n        \"output\": \" CCC=C\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Clc2ccc(Oc1ccc(cc1)N(=O)=O)c(Cl)c2\\n\",\n        \"output\": \" 3.467368504525317e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Butyl acetate\\n\",\n        \"output\": \" CCCCOC=O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][=C]\\n\",\n        \"output\": \" d-Limonene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-Aminophenol\\n\",\n        \"output\": \" Nc1ccc(O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Hexanol\\n\",\n        \"output\": \" 0.1288249551693134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1ccccc1Cl\\n\",\n        \"output\": \" 2-Chlorotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H14O4/c1-3-15-11(13)9-7-5-6-8-10(9)12(14)16-4-2/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" Diethyl phthalate \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,4-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Chloroiodobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][I]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3C(O)CC21C\\n\",\n        \"output\": \" Hydrocortisone 21-acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H17N5O/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" Atratone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Bromobenzene\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CBr\\n\",\n        \"output\": \" 0.16218100973589297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Diuron\\n\",\n        \"output\": \" InChI=1S/C9H10Cl2N2O/c1-13(2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,4,6-Trimethylphenol\\n\",\n        \"output\": \" Cc1cc(C)c(O)c(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1N(COC(=O)CCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3-Butanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Pentadecanol\\n\",\n        \"output\": \" CCCCCCCCCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][C][=C]\\n\",\n        \"output\": \" 1,3-Butadiene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethirimol\\n\",\n        \"output\": \" [C][C][C][C][C][=C][Branch1][C][C][N][=C][Branch1][Ring2][N][C][C][NH1][C][Ring1][#Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pentylcyclopentane\\n\",\n        \"output\": \" InChI=1S/C10H20/c1-2-3-4-7-10-8-5-6-9-10/h10H,2-9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][C][Branch1][C][O][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Trichlorfon\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethyl vinyl ether\\n\",\n        \"output\": \" InChI=1S/C4H8O/c1-3-5-4-2/h3H,1,4H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methanol\\n\",\n        \"output\": \" CO\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" ClCC#CCOC(=O)Nc1cccc(Cl)c1\\n\",\n        \"output\": \" 4.265795188015926e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Chlorobromobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4BrCl/c7-5-1-3-6(8)4-2-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC#C\\n\",\n        \"output\": \" 0.3890451449942806 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Prometryn\\n\",\n        \"output\": \" CSc1nc(NC(C)C)nc(NC(C)C)n1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H6O/c1-2-3/h3H,2H2,1H3\\n\",\n        \"output\": \" Ethanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC34CCC1C(CCC2=CC(=O)CCC12O)C3CCC4(O)C#C\\n\",\n        \"output\": \" Norethisterone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" N-Ethylaniline\\n\",\n        \"output\": \" 0.0199526231496888 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Malathion\\n\",\n        \"output\": \" InChI=1S/C10H19O6PS2/c1-5-15-9(11)7-8(10(12)16-6-2)19-17(18,13-3)14-4/h8H,5-7H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" o-Chlorobromobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Chlorobutane\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H\\n\",\n        \"output\": \" -0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H9NO2/c1-9-8(10)11-7-5-3-2-4-6-7/h2-6H,1H3,(H,9,10)\\n\",\n        \"output\": \" Metolcarb\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CN(C)C(=O)Oc1cc(C)nn1c2ccccc2\\n\",\n        \"output\": \" Pyrolan\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Oc2ncc1nccnc1n2\\n\",\n        \"output\": \" 2-hydroxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H10/c1-3-5-6-4-2/h1H,4-6H2,2H3\\n\",\n        \"output\": \" 0.004365158322401661 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][#N]\\n\",\n        \"output\": \" Acrylonitrile\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C22H19Cl2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\",\n        \"output\": \" 9.616122783836619e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" butacarb\\n\",\n        \"output\": \" InChI=1S/C16H25NO2/c1-15(2,3)11-8-12(16(4,5)6)10-13(9-11)19-14(18)17-7/h8-10H,1-7H3,(H,17,18)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1,4-Dinitrobenzene\\n\",\n        \"output\": \" 0.0004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][#C]\\n\",\n        \"output\": \" 1-Nonyne \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-3-5(6)7-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" Ethyl propionate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][C][C][C][Ring2][Ring1][Ring1][Ring1][S][C]\\n\",\n        \"output\": \" Progesterone\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Dialifor\\n\",\n        \"output\": \" InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" C1CCC2CCCCC2C1\\n\",\n        \"output\": \" -5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" XMC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Cc1cc(=O)[nH]c(=S)[nH]1\\n\",\n        \"output\": \" 0.0036643757464783332 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-5(9)6(10)2-4(3)8/h1-2,10H\\n\",\n        \"output\": \" 2,4,5-Trichlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)=CCCC(O)(C)C=C\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,3-Dichlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4Cl2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Neburon\\n\",\n        \"output\": \" InChI=1S/C12H16Cl2N2O/c1-3-4-7-16(2)12(17)15-9-5-6-10(13)11(14)8-9/h5-6,8H,3-4,7H2,1-2H3,(H,15,17)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" o-Chloroaniline\\n\",\n        \"output\": \" InChI=1S/C6H6ClN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Chloro-2-bromoethane\\n\",\n        \"output\": \" ClCCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethanol\\n\",\n        \"output\": \" InChI=1S/C2H6O/c1-2-3/h3H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Clonazepam\\n\",\n        \"output\": \" Clc1ccccc1C2=NCC(=O)Nc3ccc(cc23)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=Branch1][N][=C][Ring1][Branch2][C][Ring1][N][O][C][Ring1][#C][=O][C]\\n\",\n        \"output\": \" 0.0008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][Branch1][C][O][=C][Branch1][C][C][C][=C][C][Branch1][=Branch1][C][Branch1][C][C][C][=C][Ring1][O]\\n\",\n        \"output\": \" Carvacrol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H6O/c1-3-2-4-3/h3H,2H2,1H3\\n\",\n        \"output\": \" 1,2-Propylene oxide\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" 0.72443596007499 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" 2,4-Dimethylphenol\\n\",\n        \"output\": \" 0.06456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC=CC=O\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Methylparaben\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h1H,4-8H2,2H3\\n\",\n        \"output\": \" 1-Octyne \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 5,5-Diallylbarbital\\n\",\n        \"output\": \" -2.077\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][Branch1][P][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][=C][Branch1][C][C][C][=C][Ring1][#C][C]\\n\",\n        \"output\": \" 0.0005754399373371566 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,3,5,6-Tetrachlorophenol\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" DDE\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Dapsone\\n\",\n        \"output\": \" -3.094\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Methyl-3-pentanol\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" trans-1,4-Dimethylcyclohexane\\n\",\n        \"output\": \" 3.3884415613920276e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1,3-Dichloropropane\\n\",\n        \"output\": \" InChI=1S/C3H6Cl2/c4-2-1-3-5/h1-3H2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C2Cl6/c3-1(4,5)2(6,7)8\\n\",\n        \"output\": \" -3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)5(9)2-3/h1-2H\\n\",\n        \"output\": \" 1,2,3,5-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" p-Chloronitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4ClNO2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Iodoheptane\\n\",\n        \"output\": \" -4.81\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][/C][C][C][C][C][C][Ring1][=Branch1][\\\\C]\\n\",\n        \"output\": \" cis-1,2-Dimethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 1,2-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H9I/c1-2-3-4-5/h2-4H2,1H3\\n\",\n        \"output\": \" 1-Iodobutane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)\\n\",\n        \"output\": \" 4-Nitroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" Cycloheptanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=S][Branch1][Ring1][O][C][S][C][C][=Branch1][C][=O][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -4.4319999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(O)C(C)C\\n\",\n        \"output\": \" 0.19952623149688797 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Metoxuron\\n\",\n        \"output\": \" InChI=1S/C10H13ClN2O2/c1-13(2)10(14)12-7-4-5-9(15-3)8(11)6-7/h4-6H,1-3H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Diethyl sulfide\\n\",\n        \"output\": \" CCSCC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 9.332543007969905e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][C][Br][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][Branch1][C][N][=O]\\n\",\n        \"output\": \" 0.0020892961308540386 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Azintamide\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][S][C][=C][C][=C][Branch1][C][Cl][N][=N][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(9)5(10)2-3/h1-2,10H\\n\",\n        \"output\": \" 0.0021379620895022326 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C]\\n\",\n        \"output\": \" Ethion\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C][Branch2][Ring1][=C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][C][Ring1][O][C][C][C][Ring2][Ring1][C][Ring1][#C][C][C][#C]\\n\",\n        \"output\": \" norethindrone acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][O][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][Branch1][C][O][C][#C]\\n\",\n        \"output\": \" Norethisterone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3-8H,1-2H3\\n\",\n        \"output\": \" Anethole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3\\n\",\n        \"output\": \" 1,4-Dimethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,4,5-Trichlorophenol \\n\",\n        \"output\": \" Oc1cc(Cl)c(Cl)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H10O2/c1-4(2)7-5(3)6/h4H,1-3H3\\n\",\n        \"output\": \" Isopropyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Sulfanilamide\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCCCCCCO\\n\",\n        \"output\": \" 1-Tetradecanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-Fluoroacetanilide\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Methylbutan-1-ol\\n\",\n        \"output\": \" CC(C)CCO\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC=C\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C22H19Br2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\",\n        \"output\": \" -8.402000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pyrene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Methylnaphthalene\\n\",\n        \"output\": \" Cc1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][O][C][=O]\\n\",\n        \"output\": \" Isopentyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Pentanone\\n\",\n        \"output\": \" -0.19\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" DDT\\n\",\n        \"output\": \" InChI=1S/C14H9Cl5/c15-11-5-1-9(2-6-11)13(14(17,18)19)10-3-7-12(16)8-4-10/h1-8,13H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benzo[ghi]perylene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=C][Ring1][#C][C][Ring1][=N][=C][Ring1][O][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Napthol\\n\",\n        \"output\": \" InChI=1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Pentane\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Chloramphenicol\\n\",\n        \"output\": \" [O][C][C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl][C][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O]\\n\",\n        \"output\": \" Methanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Risocaine\\n\",\n        \"output\": \" CCCOC(=O)c1ccc(N)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,4-Dimethylphenol\\n\",\n        \"output\": \" InChI=1S/C8H10O/c1-6-3-4-8(9)7(2)5-6/h3-5,9H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Secobarbital\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Branch2][C][Branch1][C][C][C][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" O-Ethyl carbamate\\n\",\n        \"output\": \" CCOC(=O)N\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methazole\\n\",\n        \"output\": \" Cn2c(=O)on(c1ccc(Cl)c(Cl)c1)c2=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dichlorophen\\n\",\n        \"output\": \" InChI=1S/C13H10Cl2O2/c14-10-1-3-12(16)8(6-10)5-9-7-11(15)2-4-13(9)17/h1-4,6-7,16-17H,5H2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][N][C][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][Ring2][=C][Ring1][=N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.58921934645005e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methyl acetate\\n\",\n        \"output\": \" COC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Terbacil\\n\",\n        \"output\": \" [C][C][NH1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=Branch1][C][=O][C][=Ring1][Branch2][Cl][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" sugar\\n\",\n        \"output\": \" sugar does not have InChI\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Carbazole\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility of given compound in room temperature? ->\",\n        \"input\": \" 3-Methyl-2-butanol\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1O\\n\",\n        \"output\": \" Testosterone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" Dialifor\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H16ClO5PS/c1-4-17-21(22,18-5-2)20-10-6-7-12-11(8-10)9(3)13(15)14(16)19-12/h6-8H,4-5H2,1-3H3\\n\",\n        \"output\": \" Coumaphos\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3,4-Dichloronitrobenzene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3,4-Dimethylpyridine\\n\",\n        \"output\": \" Cc1ccncc1C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)NC1CC2CC1C3CCCC23\\n\",\n        \"output\": \" Norea\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3+\\n\",\n        \"output\": \" -2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cycluron\\n\",\n        \"output\": \" InChI=1S/C11H22N2O/c1-13(2)11(14)12-10-8-6-4-3-5-7-9-10/h10H,3-9H2,1-2H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][N][Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][Ring1][=C][=O]\\n\",\n        \"output\": \" Clomazone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Bromoheptane\\n\",\n        \"output\": \" CCCCCCCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Chloroethane\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2-Bromopropane\\n\",\n        \"output\": \" -1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility of given compound in room temperature. ->\",\n        \"input\": \" 1-Phenylethanol\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Niclosamide\\n\",\n        \"output\": \" -4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Estradiol\\n\",\n        \"output\": \" CC12CCC3C(CCc4cc(O)ccc34)C2CCC1O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Br][C][Br]\\n\",\n        \"output\": \" Dibromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H6O2/c1-3-4(5)6-2/h3H,1H2,2H3\\n\",\n        \"output\": \" 0.6025595860743578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC(Cl)(Cl)Cl\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=Branch2][Ring1][=Branch1][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Perfluidone\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" L-arabinose\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][C][C][=C][C][=C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Piperine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][N][Branch1][#Branch2][C][O][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 8.491804750363127e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" Methaqualone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Carbetamide\\n\",\n        \"output\": \" c1c(NC(=O)OC(C)C(=O)NCC)cccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C2H4Cl2/c3-1-2-4/h1-2H2\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 0.0006165950018614823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H17N5S/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" Ametryn\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 3.090295432513592e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccccc1NC(=O)c2c(O)cccc2\\n\",\n        \"output\": \" 0.0002570395782768865 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,2,3,4-Tetrahydronapthalene\\n\",\n        \"output\": \" C1CCc2ccccc2C1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCC#C\\n\",\n        \"output\": \" -1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" Fluoranthene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cccc(C)c1C\\n\",\n        \"output\": \" 1,2,3-Trimethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cyclopentene \\n\",\n        \"output\": \" C1CC=CC1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Lorazepam\\n\",\n        \"output\": \" 0.0002488857318282393 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propyl formate\\n\",\n        \"output\": \" InChI=1S/C4H8O2/c1-2-3-6-4-5/h4H,2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Br][C][Branch1][C][Br][Br]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Disulfoton\\n\",\n        \"output\": \" InChI=1S/C8H19O2PS3/c1-4-9-11(12,10-5-2)14-8-7-13-6-3/h4-8H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-2-10-7-5-8-11-6-3-4-9-12(10)11/h3-9H,2H2,1H3\\n\",\n        \"output\": \" -4.17\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Ethyl benzoate \\n\",\n        \"output\": \" 0.004786300923226385 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H27NO2/c1-4-22(24)10-8-18-16-6-5-15-11-19-14(13-23-25-19)12-20(15,2)17(16)7-9-21(18,22)3/h1,11,13,16-18,24H,5-10,12H2,2-3H3\\n\",\n        \"output\": \" Danazol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Butamben\\n\",\n        \"output\": \" InChI=1S/C11H15NO2/c1-2-3-8-14-11(13)9-4-6-10(12)7-5-9/h4-7H,2-3,8,12H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Biphenyl\\n\",\n        \"output\": \" c1ccc(cc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methoproptryne\\n\",\n        \"output\": \" [C][O][C][C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cycloheptanol\\n\",\n        \"output\": \" OC1CCCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCCCO\\n\",\n        \"output\": \" 1-Decanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Methyl formate\\n\",\n        \"output\": \" COC=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H16/c1-7-6-8(2)10(4)11(5)9(7)3/h6H,1-5H3\\n\",\n        \"output\": \" Pentamethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Butanone\\n\",\n        \"output\": \" [C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H16N4O2S/c1-10(2,3)7-11-12-8(17-7)14-6(15)5-13(4)9(14)16/h6,15H,5H2,1-4H3\\n\",\n        \"output\": \" Buthidazole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-methylpteridine\\n\",\n        \"output\": \" InChI=1S/C7H6N4/c1-5-10-4-6-7(11-5)9-3-2-8-6/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Hexanoyloxymethylphenyltoin\\n\",\n        \"output\": \" O=C1N(COC(=O)CCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Clc1ccccc1c2ccccc2\\n\",\n        \"output\": \" -4.54\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Ethirimol\\n\",\n        \"output\": \" InChI=1S/C11H19N3O/c1-4-6-7-9-8(3)13-11(12-5-2)14-10(9)15/h4-7H2,1-3H3,(H2,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 4-Methylpentanol\\n\",\n        \"output\": \" CC(C)CCCO\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Difenoxuron\\n\",\n        \"output\": \" COc2ccc(Oc1ccc(NC(=O)N(C)C)cc1)cc2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Clc1cc(c(Cl)c(Cl)c1Cl)c2cc(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" -9.16\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Cycloheptanol\\n\",\n        \"output\": \" 0.1318256738556407 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Fenuron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Nc1cccc(Cl)c1\\n\",\n        \"output\": \" -1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CCC(C)C\\n\",\n        \"output\": \" -2.658\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,5-Dimethlnapthalene\\n\",\n        \"output\": \" Cc1cccc2c(C)cccc12\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC1CCCC1\\n\",\n        \"output\": \" Methylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Erythritol\\n\",\n        \"output\": \" InChI=1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2-Heptanol \\n\",\n        \"output\": \" CCCCCC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1cc(O)c(O)c2OCC3(O)CC4=CC(=O)C(O)=CC4=C3c21\\n\",\n        \"output\": \" hematein\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benzo(j)fluoranthene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][C][=C][C][Ring1][#C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H12N2S/c1-3-6-5(8)7-4-2/h3-4H2,1-2H3,(H2,6,7,8)\\n\",\n        \"output\": \" -1.46\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][S][C][=N][N][=C][Branch1][=Branch2][C][=Branch1][C][=O][N][Ring1][#Branch1][N][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.005584701947368306 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-6(2,3)5-7/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" 2,2-Dimethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propanil\\n\",\n        \"output\": \" InChI=1S/C9H9Cl2NO/c1-2-9(13)12-6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3,(H,12,13)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H10N2O4/c16-10-6-5-9(11(17)14-10)15-12(18)7-3-1-2-4-8(7)13(15)19/h1-4,9H,5-6H2,(H,14,16,17)\\n\",\n        \"output\": \" Thalidomide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Tetrahydrofurane \\n\",\n        \"output\": \" [C][C][C][O][C][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Oc1cc(Cl)ccc1Oc2ccc(Cl)cc2Cl\\n\",\n        \"output\": \" -4.46\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methane\\n\",\n        \"output\": \" InChI=1S/CH4/h1H4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,3,5-Trimethylbenzene \\n\",\n        \"output\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccc2c(c1)ccc3c4ccccc4ccc23\\n\",\n        \"output\": \" Chrysene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Methyl t-butyl ether \\n\",\n        \"output\": \" 0.5754399373371569 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H10/c1-7-5-3-4-6-8(7)2/h3-6H,1-2H3\\n\",\n        \"output\": \" -2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(OC(=O)Nc1cccc(Cl)c1)C#C\\n\",\n        \"output\": \" -2.617\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][Cl]\\n\",\n        \"output\": \" Dichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Diallate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][=Branch1][Ring1][=C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" -6.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][Ring2][C][C][=C][=C][C][=C][Ring1][=Branch2][O]\\n\",\n        \"output\": \" Eugenol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" OC1CCCCC1\\n\",\n        \"output\": \" -0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" Salicylamide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Oc1cccc(O)c1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Propanoyloxymethylphenytoin\\n\",\n        \"output\": \" InChI=1S/C19H18N2O4/c1-2-16(22)25-13-21-17(23)19(20-18(21)24,14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-12H,2,13H2,1H3,(H,20,24)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" C1N(C(=O)NCC(C)C)C(=O)NC1\\n\",\n        \"output\": \" 0.00707945784384138 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][P][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.0001599558028614668 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzo(j)fluoranthene\\n\",\n        \"output\": \" c1ccc2c3c(ccc2c1)c4cccc5cccc3c45\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 2-Nitropropane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cycloheptane\\n\",\n        \"output\": \" C1CCCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Rovral\\n\",\n        \"output\": \" 4.2072662838444376e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CH6N2/c1-3-2/h3H,2H2,1H3\\n\",\n        \"output\": \" 21.87761623949553 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" trans-2-Heptene \\n\",\n        \"output\": \" CCCC/C=C/C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" N,N-Dimethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC(C)CCO\\n\",\n        \"output\": \" 3-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C11H16N2O3/c14-8-11(9(15)13-10(16)12-8)6-4-2-1-3-5-7-11/h1-7H2,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" 0.0010423174293933046 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Mecarbam\\n\",\n        \"output\": \" 0.0030338911841942687 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-6(4-2)5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 0.06760829753919818 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][C][C][C][C][Ring1][Branch2][Ring1][Branch1]\\n\",\n        \"output\": \" -3.1710000000000003\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" brompyrazone\\n\",\n        \"output\": \" InChI=1S/C10H8BrN3O/c11-9-8(12)6-13-14(10(9)15)7-4-2-1-3-5-7/h1-6H,12H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Pyrazon\\n\",\n        \"output\": \" -2.878\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-butenal\\n\",\n        \"output\": \" [C][C][=C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 5-Ethyl-5-isopropylbarbituric acid\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CC\\n\",\n        \"output\": \" Barbital\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C]\\n\",\n        \"output\": \" Chloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Pentanol\\n\",\n        \"output\": \" CCCC(C)O\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dialifor\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][Branch1][Ring1][C][Cl][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12O2/c1-5(2)4-8-6(3)7/h5H,4H2,1-3H3\\n\",\n        \"output\": \" Isobutyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CNc2cnn(c1cccc(c1)C(F)(F)F)c(=O)c2Cl\\n\",\n        \"output\": \" norflurazon\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)CC(C)(C)O\\n\",\n        \"output\": \" 0.12022644346174127 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)\\n\",\n        \"output\": \" 2.0892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1cnc2c(c1)ccc3ncccc23\\n\",\n        \"output\": \" 1,7-phenantroline\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Hexestrol\\n\",\n        \"output\": \" CCC(C(CC)c1ccc(O)cc1)c2ccc(O)cc2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cc(no1)C(=O)NNCc2ccccc2\\n\",\n        \"output\": \" Isocarboxazid\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dexamethasone\\n\",\n        \"output\": \" CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ncc(N(=O)=O)n1CCO\\n\",\n        \"output\": \" Metronidazole\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Triadimefon\\n\",\n        \"output\": \" CC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)n2cncn2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Cyclohexadiene\\n\",\n        \"output\": \" C1C=CCC=C1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Heptanol \\n\",\n        \"output\": \" CCCCC(O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Hexene-3-ol\\n\",\n        \"output\": \" CCCC(O)C=C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3\\n\",\n        \"output\": \" -0.8759999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)C(Nc1ccc(cc1Cl)C(F)(F)F)C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" 9.931160484209335e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3\\n\",\n        \"output\": \" 0.00023442288153199226 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" O(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" -3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14N4O4/c1-12-8-7(9(17)13(2)10(12)18)14(5-11-8)3-6(16)4-15/h5-6,15-16H,3-4H2,1-2H3\\n\",\n        \"output\": \" Dyphylline\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" soprano\\n\",\n        \"output\": \" soprano does not have compound\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCOC(C)C\\n\",\n        \"output\": \" -1.34\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccc(C=O)cc1\\n\",\n        \"output\": \" p-Hydroxybenzaldehyde \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCN(=O)=O\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2-Heptanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethyl heptanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][=Branch2][C]\\n\",\n        \"output\": \" 0.0001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Propyl propanoate\\n\",\n        \"output\": \" InChI=1S/C6H12O2/c1-3-4-5-6(7)8-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)c1ccccc1C\\n\",\n        \"output\": \" -3.76\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Cl)C(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" DDD\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Napthylamine\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" m-Methylaniline\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Androsterone\\n\",\n        \"output\": \" CC12CCC(O)CC1CCC3C2CCC4(C)C3CCC4=O\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 2,2',3,4,4',5',6-PCB\\n\",\n        \"output\": \" -7.92\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,3-Dimethylpentane\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Cl]\\n\",\n        \"output\": \" 2-Chlorobutane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1occc1C(=O)Nc2ccccc2\\n\",\n        \"output\": \" -3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C5H8/c1-3-5-4-2/h1H,4-5H2,2H3\\n\",\n        \"output\": \" -1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][Branch2][C][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=N][=O]\\n\",\n        \"output\": \" Amobarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dienestrol\\n\",\n        \"output\": \" [C][C][=C][Branch1][P][C][=Branch1][Ring1][=C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" CC12CC(O)C3C(CCC4=CC(=O)C=CC34C)C2CCC1(O)C(=O)CO\\n\",\n        \"output\": \" -3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 5-Nonanone\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][C][C][Branch1][C][O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.013273944577297402 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" 1,3-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCBr\\n\",\n        \"output\": \" 1-Bromoheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,4,5-Trichlorophenol \\n\",\n        \"output\": \" -2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,4-Dibromobenzene\\n\",\n        \"output\": \" -4.07\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-3-7(2)5-8(9)4-6/h3-5,9H,1-2H3\\n\",\n        \"output\": \" 3,5-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Clc1ccc2ccccc2c1\\n\",\n        \"output\": \" -4.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.9120108393559098 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)\\n\",\n        \"output\": \" Thiourea\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" dibutyl sebacate\\n\",\n        \"output\": \" InChI=1S/C18H34O4/c1-3-5-15-21-17(19)13-11-9-7-8-10-12-14-18(20)22-16-6-4-2/h3-16H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Methyl nonanoate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2ccc(F)c(Oc3ccccc3)c2\\n\",\n        \"output\": \" -7.337000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Cycloheptane\\n\",\n        \"output\": \" InChI=1S/C7H14/c1-2-4-6-7-5-3-1/h1-7H2\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Buthidazole\\n\",\n        \"output\": \" InChI=1S/C10H16N4O2S/c1-10(2,3)7-11-12-8(17-7)14-6(15)5-13(4)9(14)16/h6,15H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 5-Methyl-5-ethylbarbituric acid\\n\",\n        \"output\": \" 0.0591561634175474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][C][=Branch1][C][=O][O][C][C][Ring1][=Branch1][C][=Ring1][=C]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Parathion\\n\",\n        \"output\": \" InChI=1S/C10H14NO5PS/c1-3-14-17(18,15-4-2)16-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H3Cl2NO2/c7-4-2-1-3-5(6(4)8)9(10)11/h1-3H\\n\",\n        \"output\": \" 2,3-Dichloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][N][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][N][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Quinethazone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Methoxybenzaldehyde\\n\",\n        \"output\": \" COc1ccc(C=O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCC\\n\",\n        \"output\": \" Heptane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Hexachloroethane\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][Branch1][=N][C][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Thalidomide\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c1cncnc1\\n\",\n        \"output\": \" Pyrimidine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)\\n\",\n        \"output\": \" 0.001475706533275893 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methoxychlor\\n\",\n        \"output\": \" COc1ccc(cc1)C(c2ccc(OC)cc2)C(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" 2-Methyl-1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,3,5,6-Tetrachlorophenol\\n\",\n        \"output\": \" Oc1c(Cl)c(Cl)cc(Cl)c1Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,4,6-Trinitrotoluene\\n\",\n        \"output\": \" InChI=1S/C7H5N3O6/c1-4-6(9(13)14)2-5(8(11)12)3-7(4)10(15)16/h2-3H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Acetonitrile\\n\",\n        \"output\": \" CC#N\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCO\\n\",\n        \"output\": \" Ethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" 2,4,5-Trichlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C3H8O2/c1-4-3-5-2/h3H2,1-2H3\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][Branch1][#Branch2][C][O][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3-Butanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCI\\n\",\n        \"output\": \" 0.025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Flucytosine\\n\",\n        \"output\": \" Nc1nc(=O)[nH]cc1F\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Isopropalin\\n\",\n        \"output\": \" -6.49\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3+\\n\",\n        \"output\": \" trans-2-Pentene \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C10H21NOS/c1-4-7-8-11(6-3)10(12)13-9-5-2/h4-9H2,1-3H3\\n\",\n        \"output\": \" 0.0002951209226666387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.0044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -5.89\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][N][=N][C][Ring1][=N][=N][Ring2][Ring1][C]\\n\",\n        \"output\": \" Triamterene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,3,5-Trinitrobenzene\\n\",\n        \"output\": \" InChI=1S/C6H3N3O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc1nc(=O)[nH]cc1F\\n\",\n        \"output\": \" Flucytosine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" Fluorometuron\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCC2NC(=O)c1cc(c(Cl)cc1N2)S(N)(=O)=O\\n\",\n        \"output\": \" Quinethazone\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Phenytoin\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][=Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H18ClN5/c1-5-16(6-2)10-14-8(11)13-9(15-10)12-7(3)4/h7H,5-6H2,1-4H3,(H,12,13,14,15)\\n\",\n        \"output\": \" Ipazine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H32O4S/c1-14(25)29-19-13-15-12-16(26)4-8-22(15,2)17-5-9-23(3)18(21(17)19)6-10-24(23)11-7-20(27)28-24/h12,17-19,21H,4-11,13H2,1-3H3\\n\",\n        \"output\": \" Spironolactone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Cl]\\n\",\n        \"output\": \" Dimecron\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Phoxim\\n\",\n        \"output\": \" InChI=1S/C12H15N2O3PS/c1-3-15-18(19,16-4-2)17-14-12(10-13)11-8-6-5-7-9-11/h5-9H,3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Iodomethane\\n\",\n        \"output\": \" -1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/CH3I/c1-2/h1H3\\n\",\n        \"output\": \" 0.1 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H\\n\",\n        \"output\": \" 3,4-Dichloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Caproaldehyde\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][S][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Butane\\n\",\n        \"output\": \" 0.0026915348039269166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O][C][Branch1][C][N][=O]\\n\",\n        \"output\": \" Methocarbamol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Flucythrinate\\n\",\n        \"output\": \" 1.33045441797809e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCN(CC)C(=S)SSC(=S)N(CC)CC\\n\",\n        \"output\": \" 1.3803842646028839e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Hexanone\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-3-4-5-6(2)7/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Flutriafol\\n\",\n        \"output\": \" InChI=1S/C16H13F2N3O/c17-13-7-5-12(6-8-13)16(22,9-21-11-19-10-20-21)14-3-1-2-4-15(14)18/h1-8,10-11,22H,9H2\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][C][C][C][N][Ring1][Branch1]\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1ccc2ncccc2c1\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Octanol\\n\",\n        \"output\": \" 0.010471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.010715193052376065 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Nitrofen\\n\",\n        \"output\": \" -5.46\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H18O/c1-3-5-7-9(10)8-6-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][#C]\\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COC(C)(C)C\\n\",\n        \"output\": \" Methyl t-butyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-Pentene-1-ol\\n\",\n        \"output\": \" [O][C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C15H14F3N3O4S2/c16-15(17,18)10-7-11-13(8-12(10)26(19,22)23)27(24,25)21-14(20-11)6-9-4-2-1-3-5-9/h1-5,7-8,14,20-21H,6H2,(H2,19,22,23)\\n\",\n        \"output\": \" Bendroflumethiazide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" hematein\\n\",\n        \"output\": \" 0.001995262314968879 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1ccc(O)cc1C\\n\",\n        \"output\": \" 0.04168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3\\n\",\n        \"output\": \" N-Methylaniline \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Pyrolan\\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H14/c1-3-5-7-8-6-4-2/h1H,4-8H2,2H3\\n\",\n        \"output\": \" -3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Altretamine\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H8N2/c1-3-9-5-6-11-10(4-2-7-13-11)12(9)14-8-1/h1-8H\\n\",\n        \"output\": \" 1,7-phenantroline\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Pyrene\\n\",\n        \"output\": \" -6.176\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" glucose\\n\",\n        \"output\": \" 5.495408738576246 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCl\\n\",\n        \"output\": \" 1-Chloropentane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Nerol\\n\",\n        \"output\": \" InChI=1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7-\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Ethyl-p-aminobenzoate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Metribuzin\\n\",\n        \"output\": \" [C][S][C][=N][N][=C][Branch1][=Branch2][C][=Branch1][C][=O][N][Ring1][#Branch1][N][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Thiophene\\n\",\n        \"output\": \" InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Prednisolone\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H6Cl4/c13-9-5-1-3-7(11(9)15)8-4-2-6-10(14)12(8)16/h1-6H\\n\",\n        \"output\": \" 2,2',3,3'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.00021379620895022324 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Chloronapthalene\\n\",\n        \"output\": \" 7.244359600749906e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Buturon\\n\",\n        \"output\": \" CC(C#C)N(C)C(=O)Nc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,3-Dimethyl-1,3-Butadiene\\n\",\n        \"output\": \" [C][C][=Branch1][C][=C][C][=Branch1][C][=C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H16N2O3/c1-5(2)10(6(3)4)7(13)11-9(15)12-8(10)14/h5-6H,1-4H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 5,5-Diisopropylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cncc(C)c1\\n\",\n        \"output\": \" 3,5-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)CCC)CC=C\\n\",\n        \"output\": \" 0.0044055486350655345 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H5Cl/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" Chlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Butyraldehyde\\n\",\n        \"output\": \" InChI=1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Barban\\n\",\n        \"output\": \" ClCC#CCOC(=O)Nc1cccc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 6-Methylchrysene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H6/c1-3-2/h3H,1H2,2H3\\n\",\n        \"output\": \" Propylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Toluenesulfonamide \\n\",\n        \"output\": \" InChI=1S/C7H9NO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Chloroheptane\\n\",\n        \"output\": \" CCCCCCCCl\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" d-inositol\\n\",\n        \"output\": \" InChI=1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Methyl-2-heptanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 10.471285480508996 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2,4-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H3Br3/c7-4-1-5(8)3-6(9)2-4/h1-3H\\n\",\n        \"output\": \" 1,3,5-Tribromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3,4-Dimethylphenol\\n\",\n        \"output\": \" Cc1ccc(O)cc1C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C20H14/c1-2-7-16-13(4-1)8-10-17-18-11-9-14-5-3-6-15(20(14)18)12-19(16)17/h1-8,10,12H,9,11H2\\n\",\n        \"output\": \" 1.4125375446227554e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H11Cl/c1-2-3-4-5-6/h2-5H2,1H3\\n\",\n        \"output\": \" 1-Chloropentane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H7Br/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\\n\",\n        \"output\": \" 2-Bromonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Metolcarb\\n\",\n        \"output\": \" 0.01573982864466219 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-butenal\\n\",\n        \"output\": \" CC=CC=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Eugenol\\n\",\n        \"output\": \" [C][O][C][=C][C][Branch1][Ring2][C][C][=C][=C][C][=C][Ring1][=Branch2][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H21N2O3PS/c1-6-15-18(19,16-7-2)17-11-8-10(5)13-12(14-11)9(3)4/h8-9H,6-7H2,1-5H3\\n\",\n        \"output\": \" Diazinon\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Benzoxazole\\n\",\n        \"output\": \" InChI=1S/C7H5NO/c1-2-4-7-6(3-1)8-5-9-7/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][Branch1][Ring1][O][C][=C][C][=C][Branch1][Ring2][C][C][=C][C][=C][Ring1][O]\\n\",\n        \"output\": \" Estragole\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8Cl4N2/c9-5-3(1-13)6(10)8(12)7(11)4(5)2-14\\n\",\n        \"output\": \" Chlorothalonil\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Bensulide\\n\",\n        \"output\": \" -4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,3-Dinitrobenzene\\n\",\n        \"output\": \" -2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C)C\\n\",\n        \"output\": \" 5,5-Dimethylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccccc1Cl\\n\",\n        \"output\": \" -3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H18N2O4/c1-2-16(22)25-13-21-17(23)19(20-18(21)24,14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-12H,2,13H2,1H3,(H,20,24)\\n\",\n        \"output\": \" 3-Propanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" C1(=O)NC(=O)NC(=O)C1(O)C2(O)C(=O)NC(=O)NC2(=O)\\n\",\n        \"output\": \" 0.010232929922807542 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H7NO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3\\n\",\n        \"output\": \" p-Nitroanisole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOC2Oc1ccc(OS(C)(=O)=O)cc1C2(C)C\\n\",\n        \"output\": \" ethofumesate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Isoprocarb\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H17ClN3O3PS/c1-5-14-17(18,15-6-2)16-9-11-8(10)13(12-9)7(3)4/h7H,5-6H2,1-4H3\\n\",\n        \"output\": \" -3.658\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-4(2)6-3-5/h3-4H,1-2H3\\n\",\n        \"output\": \" Isopropyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Acenapthylene\\n\",\n        \"output\": \" C1=Cc2cccc3cccc1c23\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCCCCC(=O)OC\\n\",\n        \"output\": \" 0.0004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Fenuron\\n\",\n        \"output\": \" InChI=1S/C9H12N2O/c1-11(2)9(12)10-8-6-4-3-5-7-8/h3-7H,1-2H3,(H,10,12)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H10N2O3/c1-3-7(2)4(10)8-6(12)9-5(7)11/h3H2,1-2H3,(H2,8,9,10,11,12)\\n\",\n        \"output\": \" 5-Methyl-5-ethylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COP(=S)(OC)Oc1ccc(cc1Cl)N(=O)=O\\n\",\n        \"output\": \" Dicapthon\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cyhalothrin\\n\",\n        \"output\": \" CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C2H2/c1-2/h1-2H\\n\",\n        \"output\": \" Ethyne\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][=Branch2][Branch1][C][O][C][Branch1][C][O][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][=Branch2][=O]\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Eriodictyol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nitroethane\\n\",\n        \"output\": \" [C][C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Methyl-1-Butene\\n\",\n        \"output\": \" CCC(=C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1CCC=CC1\\n\",\n        \"output\": \" Cyclohexene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.001995262314968879 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Chlorbufam\\n\",\n        \"output\": \" 0.0024154608344449406 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H20/c1-8(2)6-7-9(3,4)5/h8H,6-7H2,1-5H3\\n\",\n        \"output\": \" 2,2,5-Trimethylhexane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][=Branch1][N][Branch1][C][C][C][C][Branch1][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Aminocarb\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Hexanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Chloroacetonitrile\\n\",\n        \"output\": \" [Cl][C][C][#N]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Pyrimidine\\n\",\n        \"output\": \" c1cncnc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1cc(C)c2ccccc2c1\\n\",\n        \"output\": \" 1,3-Dimethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,4-Dichlorophenol \\n\",\n        \"output\": \" Oc1ccc(Cl)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1c2ccccc2c3ccc4ccccc4c13\\n\",\n        \"output\": \" Benzo(a)fluorene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Propanil\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][=O]\\n\",\n        \"output\": \" Caproaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Anthraquinone\\n\",\n        \"output\": \" InChI=1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-4-8-7(2)5-6/h3-5H,1-2H3\\n\",\n        \"output\": \" 2.3988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Pyrazinamide\\n\",\n        \"output\": \" NC(=O)c1cnccn1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][/C][C][C][C][Branch1][C][\\\\C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" trans-1,4-Dimethylcyclohexane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 2,3-Dichloronitrobenzene\\n\",\n        \"output\": \" -3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCl\\n\",\n        \"output\": \" 0.0018620871366628676 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,4-Dimethyl-2-pentanol \\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-6(2)5-7(3,4)8/h6,8H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Butabarbital\\n\",\n        \"output\": \" InChI=1S/C10H16N2O3/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Hexachloroethane\\n\",\n        \"output\": \" InChI=1S/C2Cl6/c3-1(4,5)2(6,7)8\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H18N2O3/c1-18(2)16(19)17-12-4-6-14(7-5-12)21-15-10-8-13(20-3)9-11-15/h4-11H,1-3H3,(H,17,19)\\n\",\n        \"output\": \" Difenoxuron\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -4.328\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cypermethrin\\n\",\n        \"output\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H10N2O3/c1-3-4-8(2)5(11)9-7(13)10-6(8)12/h3H,1,4H2,2H3,(H2,9,10,11,12,13)\\n\",\n        \"output\": \" -1.16\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 3,4-Dichlorophenol\\n\",\n        \"output\": \" -1.25\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Fenothiocarb\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][S][C][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Fc1cccc(Br)c1\\n\",\n        \"output\": \" m-Fluorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H6N2O5/c1-4-2-5(8(11)12)3-6(7(4)10)9(13)14/h2-3,10H,1H3\\n\",\n        \"output\": \" DNOC\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3,4-Dichlorophenol\\n\",\n        \"output\": \" Oc1ccc(Cl)c(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.004897788193684461 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" p-Chloroacetanilide\\n\",\n        \"output\": \" -2.843\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Phoxim\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][N][=C][Branch1][Ring1][C][#N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Isopropylbenzene \\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][=Branch2][C][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" Pencycuron\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ncnc2nccnc12\\n\",\n        \"output\": \" 4-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H\\n\",\n        \"output\": \" 0.03548133892335755 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H6N2O4/c1-5-6(8(10)11)3-2-4-7(5)9(12)13/h2-4H,1H3\\n\",\n        \"output\": \" 2,6-Dinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" -1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3\\n\",\n        \"output\": \" 3.9627803425543934e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dimethyl sulfide\\n\",\n        \"output\": \" [C][S][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Propanol\\n\",\n        \"output\": \" InChI=1S/C3H8O/c1-2-3-4/h4H,2-3H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Barbital\\n\",\n        \"output\": \" -2.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Triclosan\\n\",\n        \"output\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H27FO6/c1-18-6-5-12(24)7-11(18)3-4-13-14-8-15(25)21(28,17(27)10-23)19(14,2)9-16(26)20(13,18)22/h5-7,13-16,23,25-26,28H,3-4,8-10H2,1-2H3\\n\",\n        \"output\": \" Triamcinolone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H4N2/c1-2-4-6-5-3-1/h1-4H\\n\",\n        \"output\": \" Pyridazine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-ethylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)CC=C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" N-Methylaniline \\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ccc(O)cc1C\\n\",\n        \"output\": \" 3,4-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Phenylhydrazine\\n\",\n        \"output\": \" NNc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,4-Dimethylpyridine\\n\",\n        \"output\": \" Cc1ccnc(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Fluorobenzene\\n\",\n        \"output\": \" -1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.001 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H3Br3/c7-4-1-2-5(8)6(9)3-4/h1-3H\\n\",\n        \"output\": \" 1,2,4-tribromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C]\\n\",\n        \"output\": \" 0.6509999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][Branch1][C][O][C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.004786300923226385 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C1Cc2c3c1cccc3cc4c2ccc5ccccc54\\n\",\n        \"output\": \" Cholanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" m-Xylene \\n\",\n        \"output\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Methylcyclopentane\\n\",\n        \"output\": \" InChI=1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ditalimfos\\n\",\n        \"output\": \" CCOP(=S)(OCC)N2C(=O)c1ccccc1C2=O\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2,4-tribromobenzene\\n\",\n        \"output\": \" c1(Br)c(Br)cc(Br)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Caproaldehyde\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1-Ethylnaphthalene \\n\",\n        \"output\": \" InChI=1S/C12H12/c1-2-10-7-5-8-11-6-3-4-9-12(10)11/h3-9H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-Methyl-2-pentanol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Bromopentane\\n\",\n        \"output\": \" [C][C][C][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Phorate\\n\",\n        \"output\": \" -4.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Isopropyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Nc1ccc(cc1)c2ccc(N)cc2\\n\",\n        \"output\": \" p,p'-Biphenyldiamine \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(=O)C(=CCOP(=O)(OC)OC)Cl\\n\",\n        \"output\": \" Dimecron\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Trifluralin\\n\",\n        \"output\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Pebulate\\n\",\n        \"output\": \" InChI=1S/C10H21NOS/c1-4-7-8-11(6-3)10(12)13-9-5-2/h4-9H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][C]\\n\",\n        \"output\": \" Phorate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-3-5-6-7(8)4-2/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 3-Heptanol \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Inosine\\n\",\n        \"output\": \" -1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-ethylbarbital\\n\",\n        \"output\": \" -2.253\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H16ClN3O2/c1-14(2,3)12(19)13(18-9-16-8-17-18)20-11-6-4-10(15)5-7-11/h4-9,13H,1-3H3\\n\",\n        \"output\": \" 0.0002454708915685031 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Chlorotoluron\\n\",\n        \"output\": \" 0.0003467368504525317 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Toluenesulfonamide \\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Diiodomethane\\n\",\n        \"output\": \" 0.004570881896148752 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diisopropyl ether \\n\",\n        \"output\": \" [C][C][Branch1][C][C][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Methylbutan-2-ol\\n\",\n        \"output\": \" 1.4125375446227544 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Equilenin\\n\",\n        \"output\": \" 5.754399373371567e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" kebuzone\\n\",\n        \"output\": \" InChI=1S/C19H18N2O3/c1-14(22)12-13-17-18(23)20(15-8-4-2-5-9-15)21(19(17)24)16-10-6-3-7-11-16/h2-11,17H,12-13H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H7Cl/c1-6-4-2-3-5-7(6)8/h2-5H,1H3\\n\",\n        \"output\": \" 0.0003019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCC(C)(C)CO\\n\",\n        \"output\": \" 2,2-Dimethylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C27H37FO6/c1-5-6-7-23(33)34-27(22(32)15-29)16(2)12-20-19-9-8-17-13-18(30)10-11-24(17,3)26(19,28)21(31)14-25(20,27)4/h10-11,13,16,19-21,29,31H,5-9,12,14-15H2,1-4H3\\n\",\n        \"output\": \" 1.9498445997580456e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Diethyl phthalate \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=Branch1][C][=C][C][C][C][=C][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2]\\n\",\n        \"output\": \" -2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(=O)SC4CC1=CC(=O)CCC1(C)C5CCC2(C)C(CCC23CCC(=O)O3)C45\\n\",\n        \"output\": \" Spironolactone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -3.082\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dibutyl ether \\n\",\n        \"output\": \" [C][C][C][C][O][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.03548133892335755 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Methyl-2-butanol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-4(2)5(3)6/h4-6H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-12H2,1H3\\n\",\n        \"output\": \" 1.584893192461114e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" m-Chloronitrobenzene \\n\",\n        \"output\": \" InChI=1S/C6H4ClNO2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(C)(C)c1ccc(O)cc1\\n\",\n        \"output\": \" p-t-Butylphenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1-Bromo-2-methylpropane\\n\",\n        \"output\": \" -2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Phenylmethanol\\n\",\n        \"output\": \" InChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H6N4O/c1-12-6-3-9-5-2-8-4-10-7(5)11-6/h2-4H,1H3\\n\",\n        \"output\": \" 7-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,3-Dimethylbutane\\n\",\n        \"output\": \" InChI=1S/C6H14/c1-5(2)6(3)4/h5-6H,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3\\n\",\n        \"output\": \" -6.35\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H14/c1-3-5-7-6-4-2/h3H,1,4-7H2,2H3\\n\",\n        \"output\": \" -3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][=C][Ring1][Branch2][C]\\n\",\n        \"output\": \" 1,2,4,5-Tetramethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Nc1ccccc1N(=O)=O\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,4-Dimethylnaphthalene \\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Branch1][C][C][C][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" Menthone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCCC(=O)C\\n\",\n        \"output\": \" -3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Cortisone\\n\",\n        \"output\": \" [C][C][C][C][=Branch1][C][=O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)\\n\",\n        \"output\": \" p-Hydroxyacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCCCCC\\n\",\n        \"output\": \" Eicosane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Stirofos\\n\",\n        \"output\": \" InChI=1S/C10H9Cl4O4P/c1-16-19(15,17-2)18-10(5-11)6-3-8(13)9(14)4-7(6)12/h3-5H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][Branch1][Ring1][C][C][C][C][C][C]\\n\",\n        \"output\": \" -6.96\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 1-Methylfluorene\\n\",\n        \"output\": \" 6.025595860743581e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" -3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" C1CCC2CCCCC2C1\\n\",\n        \"output\": \" Decalin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H14O2/c1-2-3-5-8-6-4-7/h7H,2-6H2,1H3\\n\",\n        \"output\": \" 2-Butoxyethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propylbenzene \\n\",\n        \"output\": \" CCCc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Bromobenzene\\n\",\n        \"output\": \" Brc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12/c1-11-6-7-14-9-12-4-2-3-5-13(12)10-15(14)8-11/h2-10H,1H3\\n\",\n        \"output\": \" 2-Methylanthracene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Norethisterone\\n\",\n        \"output\": \" -4.57\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,2-Dimethylpentanol\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 1-methyluracil\\n\",\n        \"output\": \" 0.15595525028269536 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" t-Butylbenzene \\n\",\n        \"output\": \" InChI=1S/C10H14/c1-10(2,3)9-7-5-4-6-8-9/h4-8H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Tetrachloroethylene\\n\",\n        \"output\": \" ClC(=C(Cl)Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3,3-Dimethyl-1-butanol\\n\",\n        \"output\": \" CC(C)(C)CCO\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" -4.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 1,7-phenantroline\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCC(=O)OCC\\n\",\n        \"output\": \" Ethyl nonanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H15N3O2/c1-6(2)5-10-8(13)11-4-3-9-7(11)12/h6H,3-5H2,1-2H3,(H,9,12)(H,10,13)\\n\",\n        \"output\": \" 0.00707945784384138 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCOP(=S)(OCC)ON=C(C#N)c1ccccc1\\n\",\n        \"output\": \" 1.374041975012515e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClCCl\\n\",\n        \"output\": \" Dichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pentyl acetate\\n\",\n        \"output\": \" CCCCCOC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 4-Chloroanisole\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-6(2)5-7(3)4/h6-7H,5H2,1-4H3\\n\",\n        \"output\": \" 2,4-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][#C]\\n\",\n        \"output\": \" Chlorbufam\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][O][C][=Branch1][C][=O][C][Branch1][C][Cl][=C][Branch1][C][C][C][Ring1][=Branch2][=C][Ring1][=N]\\n\",\n        \"output\": \" Coumaphos\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" NC(=O)c1ccccc1O\\n\",\n        \"output\": \" o-Hydroxybenzamide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" m-Chloroaniline\\n\",\n        \"output\": \" Nc1cccc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O]\\n\",\n        \"output\": \" -3.9530000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H14/c1-2-4-6-7-5-3-1/h1-7H2\\n\",\n        \"output\": \" Cycloheptane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,4-Dimethylpyridine\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-3-4-8-7(2)5-6/h3-5H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C3H7Br/c1-2-3-4/h2-3H2,1H3\\n\",\n        \"output\": \" 1-Bromopropane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C18H20O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3-5,10,14,16,19H,2,6-9H2,1H3\\n\",\n        \"output\": \" Equilin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.06165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Estradiol\\n\",\n        \"output\": \" InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" c3ccc2nc1ccccc1cc2c3\\n\",\n        \"output\": \" 0.00021379620895022324 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C22H28O3/c1-4-22(25-14(2)23)12-10-20-19-7-5-15-13-16(24)6-8-17(15)18(19)9-11-21(20,22)3/h1,13,17-20H,5-12H2,2-3H3\\n\",\n        \"output\": \" 1.584893192461114e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCC(C)CC\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" C1c2ccccc2c3cc4ccccc4cc13\\n\",\n        \"output\": \" 9.120108393559115e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" p-Toluenesulfonamide \\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H4Br2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3\\n\",\n        \"output\": \" m-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ethyl butyrate\\n\",\n        \"output\": \" CCCCCOC(=O)CC\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Phenacetin\\n\",\n        \"output\": \" [C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 0.0018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCC(=O)C\\n\",\n        \"output\": \" 2-Nonanone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][#C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][C][=N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" Amitraz\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Eicosane\\n\",\n        \"output\": \" 6.729766562843168e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" p-Chloroaniline\\n\",\n        \"output\": \" [N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][=Branch1][C][Branch1][C][C][C][C][C][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.002552701302661247 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Methylbutane\\n\",\n        \"output\": \" CCC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Benzamide\\n\",\n        \"output\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H12N2O3/c1-3-8(4-2)5(11)9-7(13)10-6(8)12/h3-4H2,1-2H3,(H2,9,10,11,12,13)\\n\",\n        \"output\": \" Barbital\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" p-benzidine\\n\",\n        \"output\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" butacarb\\n\",\n        \"output\": \" -4.24\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" norflurazon\\n\",\n        \"output\": \" [C][N][C][C][=N][N][Branch2][Ring1][Ring1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][=Ring1][P][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2]\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -4.66\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][C][=C]\\n\",\n        \"output\": \" 0.008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" -2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" ClC(Br)Br\\n\",\n        \"output\": \" 0.012589254117941675 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Br2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\",\n        \"output\": \" 1,4-Dibromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Metoxuron\\n\",\n        \"output\": \" 0.0027289777828080433 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" vamidothion\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][C][Branch1][C][C][S][C][C][S][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H8O2/c1-10-8(9)7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" 0.01412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 3-Methylcholanthrene\\n\",\n        \"output\": \" InChI=1S/C21H16/c1-13-5-8-17-15(11-13)7-9-18-19-10-6-14-3-2-4-16(21(14)19)12-20(17)18/h2-5,7-9,11-12H,6,10H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" benzhydrol\\n\",\n        \"output\": \" InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][O][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Xipamide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Ethyl benzoate \\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C18H12/c1-3-7-15-13(5-1)9-11-18-16-8-4-2-6-14(16)10-12-17(15)18/h1-12H\\n\",\n        \"output\": \" Chrysene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)\\n\",\n        \"output\": \" 9.120108393559097 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Isobutyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Prednisolone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C16H13F2N3O/c17-13-7-5-12(6-8-13)16(22,9-21-11-19-10-20-21)14-3-1-2-4-15(14)18/h1-8,10-11,22H,9H2\\n\",\n        \"output\": \" -3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Benzo(b)fluoranthene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" thioanisole\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1[nH]c(=O)n(c(=O)c1Cl)C(C)(C)C\\n\",\n        \"output\": \" -2.484\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C]\\n\",\n        \"output\": \" 2.951209226666384e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Chloronapthalene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C18H18O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h3-12,19-20H,1-2H3\\n\",\n        \"output\": \" -4.95\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 4-Chloroanisole\\n\",\n        \"output\": \" COc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Methyl-3-pentanol\\n\",\n        \"output\": \" 0.436515832240166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Benzo(b)fluoranthene\\n\",\n        \"output\": \" InChI=1S/C20H12/c1-2-7-14-13(6-1)12-19-16-9-4-3-8-15(16)18-11-5-10-17(14)20(18)19/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-6(2)4-5-9-7(3)8/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-3-5-4-2/h3,5H,4H2,1-2H3/b5-3-\\n\",\n        \"output\": \" cis-2-Pentene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Androstenedione\\n\",\n        \"output\": \" CC34CCC1C(CCC2=CC(=O)CCC12C)C3CCC4=O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 2.0892961308540408e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO\\n\",\n        \"output\": \" 2.437810818368755e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" -8.6\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Ic1cccc2ccccc12\\n\",\n        \"output\": \" 1-Iodonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][Branch1][C][F][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C]\\n\",\n        \"output\": \" 4.6025657358135534e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC1CCCCC1\\n\",\n        \"output\": \" 0.0001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H\\n\",\n        \"output\": \" 0.004570881896148752 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H8BrNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\",\n        \"output\": \" p-Bromoacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 3-Hexyne\\n\",\n        \"output\": \" [C][C][C][#C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2H4/c1-2/h1-2H2\\n\",\n        \"output\": \" 0.3981071705534972 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H12/c1-11-7-9-13(10-8-11)12-5-3-2-4-6-12/h2-10H,1H3\\n\",\n        \"output\": \" 2.39883291901949e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" 5-Ethyl-5-phenylbarbital\\n\",\n        \"output\": \" 0.004764309868054156 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Branch1][C][Br][C][Branch1][C][Cl][Branch1][C][Cl][Br]\\n\",\n        \"output\": \" Naled\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-ethylbarbital\\n\",\n        \"output\": \" InChI=1S/C11H16N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h5H,4,6H2,1-3H3,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Chloro-2-methylpropane\\n\",\n        \"output\": \" [Cl][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Santonin\\n\",\n        \"output\": \" -3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Trichloromethane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C]\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dibenzothiophene\\n\",\n        \"output\": \" InChI=1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H15N2O3PS/c1-3-15-18(19,16-4-2)17-14-12(10-13)11-8-6-5-7-9-11/h5-9H,3-4H2,1-2H3\\n\",\n        \"output\": \" -4.862\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][N][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][P][O]\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanone\\n\",\n        \"output\": \" InChI=1S/C6H12O/c1-5(7)6(2,3)4/h1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][C][=N][C][=N][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 4-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][N][=C][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3,5-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Trichloronate\\n\",\n        \"output\": \" -5.752000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" o-Fluorobromobenzene\\n\",\n        \"output\": \" Fc1ccccc1Br\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" BrC(Br)Br\\n\",\n        \"output\": \" -1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C14H24NO4PS3/c1-12(2)18-20(21,19-13(3)4)22-11-10-15-23(16,17)14-8-6-5-7-9-14/h5-9,12-13,15H,10-11H2,1-4H3\\n\",\n        \"output\": \" 6.309573444801929e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1,3,5-Trichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" COc1ccccc1O\\n\",\n        \"output\": \" o-Methoxyphenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-6(4-2)5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 2-Ethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][#C]\\n\",\n        \"output\": \" Ethyne\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" -3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.00016982436524617443 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl\\n\",\n        \"output\": \" 2.290867652767775e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethyl-p-aminobenzoate\\n\",\n        \"output\": \" CCOC(=O)c1ccc(N)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Cyclohexanol \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][Branch1][=N][O][Ring1][Branch1][C][=Branch1][C][=O][N][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Isocarboxazid\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][S][C][=Branch1][C][=S][N][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" Disulfiram\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Terbacil\\n\",\n        \"output\": \" Cc1[nH]c(=O)n(c(=O)c1Cl)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H3Cl7/c13-4-1-2-5(6(14)3-4)7-8(15)10(17)12(19)11(18)9(7)16/h1-3H\\n\",\n        \"output\": \" 2,2',3,4,4',5',6-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" p-Chloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 7.762471166286911e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-Ethyl-1-butanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-3-6(4-2)5-7/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" kebuzone\\n\",\n        \"output\": \" CC(=O)CCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethylcyclohexane\\n\",\n        \"output\": \" CCC1CCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Phenacetin\\n\",\n        \"output\": \" InChI=1S/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" ampyrone\\n\",\n        \"output\": \" [C][C][=C][Branch1][C][N][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=N][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-2-3-4-5-6-7/h7H,2-6H2,1H3\\n\",\n        \"output\": \" -1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H15N3O2/c1-6(2)5-10-8(13)11-4-3-9-7(11)12/h6H,3-5H2,1-2H3,(H,9,12)(H,10,13)\\n\",\n        \"output\": \" isocarbamid\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][I]\\n\",\n        \"output\": \" 1-Iodobutane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" p-terphenyl\\n\",\n        \"output\": \" InChI=1S/C18H14/c1-3-7-15(8-4-1)17-11-13-18(14-12-17)16-9-5-2-6-10-16/h1-14H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Thiophene\\n\",\n        \"output\": \" 0.046773514128719815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Methylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H12N2O/c1-9-8-11(14)13(12(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3\\n\",\n        \"output\": \" Antipyrene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Chloro-2-methylpropane\\n\",\n        \"output\": \" -2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Oc1c(Cl)cccc1Cl\\n\",\n        \"output\": \" 0.0162181009735893 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" -4.64\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Octane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC1COC(Cn2cncn2)(O1)c3ccc(Cl)cc3Cl\\n\",\n        \"output\": \" Propiconazole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCc1ccccn1\\n\",\n        \"output\": \" 2-Ethyl pyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Lindane\\n\",\n        \"output\": \" ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Prometryn\\n\",\n        \"output\": \" InChI=1S/C10H19N5S/c1-6(2)11-8-13-9(12-7(3)4)15-10(14-8)16-5/h6-7H,1-5H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H\\n\",\n        \"output\": \" 4.168693834703354 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][Branch1][P][C][Branch1][Ring1][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -4.43\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-6-15-12-19-17-10-4-8-13-7-3-9-16(20(13)17)18(19)11-14(15)5-1/h1-12H\\n\",\n        \"output\": \" 3.235936569296281e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.00016982436524617443 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" 1,2-Diethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2H6S/c1-3-2/h1-2H3\\n\",\n        \"output\": \" -0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" N,N-Dimethylaniline\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(=O)C\\n\",\n        \"output\": \" 3.311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCNP(=S)(OC)OC(=CC(=O)OC(C)C)C\\n\",\n        \"output\": \" Propetamphos\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H7Cl/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\\n\",\n        \"output\": \" -4.14\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H\\n\",\n        \"output\": \" 1-Napthol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCC=C\\n\",\n        \"output\": \" 1-Nonene \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" c2cnc1ncncc1n2\\n\",\n        \"output\": \" Pteridine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,3-Difluorobenzene\\n\",\n        \"output\": \" [F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(O)c1ccccc1\\n\",\n        \"output\": \" 1-Phenylethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)SC(C)C\\n\",\n        \"output\": \" -2.24\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][S][C][C][C]\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Equilin\\n\",\n        \"output\": \" [C][C][C][C][C][C][=Branch1][S][=C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][N][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 2,3-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" COP(=S)(OC)Oc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" -5.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C2H5Br/c1-2-3/h2H2,1H3\\n\",\n        \"output\": \" 0.0812830516164099 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Dibenzofurane\\n\",\n        \"output\": \" o1c2ccccc2c3ccccc13\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Atrazine\\n\",\n        \"output\": \" 0.0001412537544622754 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-4-6(2,3)5-7/h7H,4-5H2,1-3H3\\n\",\n        \"output\": \" 0.09120108393559097 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3\\n\",\n        \"output\": \" -1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Quinonamid\\n\",\n        \"output\": \" 9.332543007969906e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" linalool\\n\",\n        \"output\": \" -1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Bromonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Phenylhydrazine\\n\",\n        \"output\": \" [N][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Pentachlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 5-Allyl-5-isopropylbarbital\\n\",\n        \"output\": \" InChI=1S/C10H14N2O3/c1-4-5-10(6(2)3)7(13)11-9(15)12-8(10)14/h4,6H,1,5H2,2-3H3,(H2,11,12,13,14,15)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H9NO2S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3,(H2,8,9,10)\\n\",\n        \"output\": \" p-Toluenesulfonamide \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][#Branch2]\\n\",\n        \"output\": \" 1-Methylphenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Chloroxuron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClCC\\n\",\n        \"output\": \" Chloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Isazofos\\n\",\n        \"output\": \" -3.658\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Brc1ccccc1Br\\n\",\n        \"output\": \" -3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H8/c1-3-4-2/h3H,1,4H2,2H3\\n\",\n        \"output\": \" -1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCc1ccc(CC)cc1\\n\",\n        \"output\": \" 0.00017782794100389227 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" COCOC\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3,4-Dimethylphenol\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" DNOC\\n\",\n        \"output\": \" -1.456\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)Cl)C1C(=O)OCc2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" 5.116818355403073e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][Ring2][O][Ring1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" Propiconazole\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][O]\\n\",\n        \"output\": \" 0.07244359600749903 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" C=CC=O\\n\",\n        \"output\": \" Acrolein\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][O][C]\\n\",\n        \"output\": \" Methyl butyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Monolinuron\\n\",\n        \"output\": \" CON(C)C(=O)Nc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1cc(Cl)c(Cl)c(Cl)c1\\n\",\n        \"output\": \" 2.344228815319923e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=N][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 3,4-Dimethylpyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" OC(C(=O)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" -2.85\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H20ClN5/c1-5-16(6-2)10-13-9(12)14-11(15-10)17(7-3)8-4/h5-8H2,1-4H3\\n\",\n        \"output\": \" 3.881503659906478e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Monuron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" -2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 5.495408738576248e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=N(=O)c1cc(cc(c1)N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" 1,3,5-Trinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diazinon\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][=C][C][Branch1][C][C][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 6.456542290346549e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Triamcinolone\\n\",\n        \"output\": \" CC34CC(O)C1(F)C(CCC2=CC(=O)C=CC12C)C3CC(O)C4(O)C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Nitropropane\\n\",\n        \"output\": \" CC(C)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCOP(=S)(CC)Oc1cc(Cl)c(Cl)cc1Cl\\n\",\n        \"output\": \" 1.7701089583174183e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4F2/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" 1,3-Difluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\\n\",\n        \"output\": \" 1,2,4,5-Tetrachlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2\\n\",\n        \"output\": \" Cyclooctane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-Bromoacetanilide\\n\",\n        \"output\": \" CC(=O)Nc1ccc(Br)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCC1(C(=O)NCNC1=O)c2ccccc2\\n\",\n        \"output\": \" -2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" square\\n\",\n        \"output\": \" square does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C2H5I/c1-2-3/h2H2,1H3\\n\",\n        \"output\": \" Iodoethane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Bromonapthalene\\n\",\n        \"output\": \" [Br][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Methanol\\n\",\n        \"output\": \" 37.15352290971726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" COc1cc(cc(OC)c1O)C6C2C(COC2=O)C(OC4OC3COC(C)OC3C(O)C4O)c7cc5OCOc5cc67\\n\",\n        \"output\": \" -3.571\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][=Branch1][C][=O][O][C][Branch2][Ring2][O][C][Branch1][C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][=Branch1][Ring2][Ring1][C][C][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Betamethasone-17-valerate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Branch1][C][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Methyldymron\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][C]\\n\",\n        \"output\": \" 2.884031503126606e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC1=CCCCC1\\n\",\n        \"output\": \" 1-Methylcyclohexene \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc1cccc2ccccc12\\n\",\n        \"output\": \" 1-Napthylamine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Corticosterone\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][O][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][P][C][C][C][Ring2][Ring1][Ring2][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/CCl4/c2-1(3,4)5\\n\",\n        \"output\": \" Tetrachloromethane\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" COC(=O)c1ccccc1OC2OC(COC3OCC(O)C(O)C3O)C(O)C(O)C2O\\n\",\n        \"output\": \" Monotropitoside\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=Branch1][=Branch1][=C][Branch1][C][Cl][Cl][Cl]\\n\",\n        \"output\": \" Tetrachloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Ipazine\\n\",\n        \"output\": \" CCN(CC)c1nc(Cl)nc(NC(C)C)n1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Methyl hydrazine\\n\",\n        \"output\": \" 21.87761623949553 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Diphenylmethane\\n\",\n        \"output\": \" [C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Acrylonitrile\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H6O/c1-2-3-4-5/h2-4H,1H3\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Branch1][C][F][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][Branch1][C][C][C][Ring1][=N][Branch1][C][F][C][Branch1][C][O][C][C][Ring2][Ring1][Ring1][Branch1][C][C][C][Ring2][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" Flumethasone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C=CCCC=C\\n\",\n        \"output\": \" 1,5-Hexadiene \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H12/c1-4-5(2)3/h5H,4H2,1-3H3\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Propylisopropylether\\n\",\n        \"output\": \" [C][C][C][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Anethole\\n\",\n        \"output\": \" COc1ccc(C=CC)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-5-6-8(4-2)7-9/h8-9H,3-7H2,1-2H3\\n\",\n        \"output\": \" 2-Ethyl-1-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccccc1SC\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Chlorophenol\\n\",\n        \"output\": \" Oc1cccc(Cl)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][O]\\n\",\n        \"output\": \" 1-Butanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Carvone\\n\",\n        \"output\": \" -2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Glyceryl triacetate\\n\",\n        \"output\": \" [C][C][=Branch1][C][=O][O][C][C][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H8BrNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)\\n\",\n        \"output\": \" -3.083\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Hexanoyloxymethylphenyltoin\\n\",\n        \"output\": \" -5.886\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C]\\n\",\n        \"output\": \" -1.742\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][O][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" Cyhalothrin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H12N2O3/c1-3-5-10(6-4-2)7(13)11-9(15)12-8(10)14/h3-4H,1-2,5-6H2,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 5,5-Diallylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Carbanilide\\n\",\n        \"output\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2\\n\",\n        \"output\": \" glucose\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Pentyne\\n\",\n        \"output\": \" [C][C][C][C][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCCCCCC(=O)OC\\n\",\n        \"output\": \" methyl laurate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Phenmedipham\\n\",\n        \"output\": \" -4.805\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Methyl-3-heptanol\\n\",\n        \"output\": \" InChI=1S/C8H18O/c1-4-6-7-8(3,9)5-2/h9H,4-7H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][=N]\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H10Cl2N2O/c1-13(2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\",\n        \"output\": \" -3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" alloxantin\\n\",\n        \"output\": \" InChI=1S/C8H6N4O8/c13-1-7(19,2(14)10-5(17)9-1)8(20)3(15)11-6(18)12-4(8)16/h19-20H,(H2,9,10,13,14,17)(H2,11,12,15,16,18)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Chloronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C11H18N4O2/c1-7-8(2)12-10(14(3)4)13-9(7)17-11(16)15(5)6/h1-6H3\\n\",\n        \"output\": \" -1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCC(=O)C\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Hydroxybenzaldehyde \\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][Ring1][C][=O][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,3,5-Trinitrobenzene\\n\",\n        \"output\": \" [O][=N][=Branch1][C][=O][C][=C][C][=Branch1][=N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Methyl nonanoate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Prednisolone\\n\",\n        \"output\": \" InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h5,7,9,14-16,18,22,24,26H,3-4,6,8,10-11H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzyltrifluoride\\n\",\n        \"output\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Dibenzothiophene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1ccccc1Br\\n\",\n        \"output\": \" o-Chlorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CNC(=O)Oc1cc(C)cc(C)c1\\n\",\n        \"output\": \" XMC\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Ethyl-3-pentanol\\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-4-7(8,5-2)6-3/h8H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H\\n\",\n        \"output\": \" -5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][S][C]\\n\",\n        \"output\": \" 0.35481338923357547 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H7Cl/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" 1-Chloronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1occc1C(=O)Nc2ccccc2\\n\",\n        \"output\": \" Fenfuram\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCC#C\\n\",\n        \"output\": \" -1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H16O/c1-3-5-6-8(4-2)7-9/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" 2-Ethylhexanal\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H\\n\",\n        \"output\": \" 1.8793168168032686e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Pentachloroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Talbutal\\n\",\n        \"output\": \" InChI=1S/C11H16N2O3/c1-4-6-11(7(3)5-2)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 4-Methylpentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-6(2)4-3-5-7/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Oc1ccc(Cl)cc1\\n\",\n        \"output\": \" 4-Chlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,6-Dinitrotoluene\\n\",\n        \"output\": \" Cc1c(cccc1N(=O)=O)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Coumaphos\\n\",\n        \"output\": \" InChI=1S/C14H16ClO5PS/c1-4-17-21(22,18-5-2)20-10-6-7-12-11(8-10)9(3)13(15)14(16)19-12/h6-8H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cyclohexane\\n\",\n        \"output\": \" C1CCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" DDD\\n\",\n        \"output\": \" 6.30957344480193e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" benodanil\\n\",\n        \"output\": \" InChI=1S/C13H10INO/c14-12-9-5-4-8-11(12)13(16)15-10-6-2-1-3-7-10/h1-9H,(H,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Benzaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(=O)OC\\n\",\n        \"output\": \" 0.72443596007499 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Heptachlor\\n\",\n        \"output\": \" InChI=1S/C10H5Cl7/c11-4-2-1-3-5(4)9(15)7(13)6(12)8(3,14)10(9,16)17/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" XMC\\n\",\n        \"output\": \" 0.0026242185433844392 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" O=C2NC(=O)C1(CCC1)C(=O)N2\\n\",\n        \"output\": \" -1.655\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Tribromomethane\\n\",\n        \"output\": \" [Br][C][Branch1][C][Br][Br]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H13ClN2O2/c1-13(2)10(14)12-7-4-5-9(15-3)8(11)6-7/h4-6H,1-3H3,(H,12,14)\\n\",\n        \"output\": \" Metoxuron\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Aniline \\n\",\n        \"output\": \" InChI=1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCC(C)C\\n\",\n        \"output\": \" 2-Methylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][O]\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H16F3N3O4/c1-3-5-6-17(4-2)12-10(18(20)21)7-9(13(14,15)16)8-11(12)19(22)23/h7-8H,3-6H2,1-2H3\\n\",\n        \"output\": \" Benfluralin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCBr\\n\",\n        \"output\": \" 1-Bromopropane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-Chlorophenol \\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C2H3Cl/c1-2-3/h2H,1H2\\n\",\n        \"output\": \" Chloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" O-Ethyl carbamate\\n\",\n        \"output\": \" InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,6-Dinitrotoluene\\n\",\n        \"output\": \" [C][C][=C][Branch1][N][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Androstenedione\\n\",\n        \"output\": \" -3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Benzylchloride\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C20H26O3/c1-3-19(22)10-8-16-15-5-4-13-12-14(21)6-11-20(13,23)17(15)7-9-18(16,19)2/h1,12,15-17,22-23H,4-11H2,2H3\\n\",\n        \"output\": \" 2.691534803926914e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" ethyl cinnamate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Benzo(e)pyrene\\n\",\n        \"output\": \" 1.5848931924611143e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -5.53\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Heptanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Thymol\\n\",\n        \"output\": \" InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-7,11H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][Branch2][C][C][Branch1][C][O][C][O][C][=Ring1][#Branch2][C][Ring1][S][=O]\\n\",\n        \"output\": \" Dyphylline\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO\\n\",\n        \"output\": \" Flumethasone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C][N][Branch2][Ring1][=C][S][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][C][C][Branch1][C][C][Branch1][C][C][O][C][=Ring1][#Branch1][Ring1][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -4.71\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][O][P][=Branch1][C][=S][Branch1][Branch1][O][C][C][C][S][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" Piperophos\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCOC(=O)CCN(SN(C)C(=O)Oc1cccc2CC(C)(C)Oc21)C(C)C\\n\",\n        \"output\": \" Benfuracarb\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Propyl butyrate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Ring2][C][=C][C][C][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" Anethole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Quintozene\\n\",\n        \"output\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][N][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" -4.16\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Triamcinolone\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" o-Chloronitrobenzene\\n\",\n        \"output\": \" Clc1ccccc1N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C15H23N3O4/c1-5-7-16(8-6-2)15-13(17(19)20)9-12(11(3)4)10-14(15)18(21)22/h9-11H,5-8H2,1-4H3\\n\",\n        \"output\": \" -6.49\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Camphor\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][C][C][Ring1][=Branch1][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" p-Phenylphenol\\n\",\n        \"output\": \" Oc1ccc(cc1)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-3-9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3\\n\",\n        \"output\": \" 0.0007762471166286919 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Piperophos\\n\",\n        \"output\": \" [C][C][C][O][P][=Branch1][C][=S][Branch1][Branch1][O][C][C][C][S][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 0.19054607179632474 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Buturon\\n\",\n        \"output\": \" [C][C][Branch1][Ring1][C][#C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Tricresyl phosphate\\n\",\n        \"output\": \" InChI=1S/C21H21O4P/c1-16-11-13-19(14-12-16)23-26(22,24-20-9-6-7-17(2)15-20)25-21-10-5-4-8-18(21)3/h4-15H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 1,2-Benzenediol\\n\",\n        \"output\": \" 4.168693834703354 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CN(C)C(=O)C\\n\",\n        \"output\": \" N,N-Dimethylacetamide\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 2-Methylbutanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Prometon\\n\",\n        \"output\": \" [C][O][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Methane\\n\",\n        \"output\": \" 0.12589254117941673 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Hexamethylbenzene\\n\",\n        \"output\": \" [C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][#Branch2][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" d-Limonene\\n\",\n        \"output\": \" [C][C][=C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benomyl\\n\",\n        \"output\": \" [C][C][C][C][N][C][=Branch1][C][=O][N][C][Branch1][Branch2][N][C][=Branch1][C][=O][O][C][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,4-Difluorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4F2/c7-5-1-2-6(8)4-3-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" benzhydrol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Benfluralin\\n\",\n        \"output\": \" [C][C][C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][O][C][Branch2][Ring1][C][C][O][C][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring1][O]\\n\",\n        \"output\": \" 0.18113400926196024 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" chloropropylate\\n\",\n        \"output\": \" [C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][C][O][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" o-Nitrophenol\\n\",\n        \"output\": \" -1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" -1.8359999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H16O2/c1-3-5-6-7-8(9)10-4-2/h3-7H2,1-2H3\\n\",\n        \"output\": \" Ethyl hexanoate\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" ClC1C=CC2C1C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl\\n\",\n        \"output\": \" -6.317\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C4H9Cl/c1-3-4(2)5/h4H,3H2,1-2H3\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C3H7Cl/c1-3(2)4/h3H,1-2H3\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][C][=C][C][=C][C][=C][C][=C][C][Branch1][=N][C][=Branch1][Branch1][=C][Ring2][Ring1][C][C][Ring1][P][=Ring1][=N][=C][Ring1][=Branch2][Ring1][=N]\\n\",\n        \"output\": \" Perylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" hydrobenzoin\\n\",\n        \"output\": \" c1ccccc1C(O)C(O)c2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc3cc2nc1c(=O)[nH]c(=O)nc1n(CC(O)C(O)C(O)CO)c2cc3C\\n\",\n        \"output\": \" 0.00020653801558105292 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlordane\\n\",\n        \"output\": \" ClC1CC2C(C1Cl)C3(Cl)C(=C(Cl)C2(Cl)C3(Cl)Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,1,2,2-Tetrachloroethane\\n\",\n        \"output\": \" InChI=1S/C2H2Cl4/c3-1(4)2(5)6/h1-2H\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Nc3nc(N)c2nc(c1ccccc1)c(N)nc2n3\\n\",\n        \"output\": \" -2.404\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" 3-Pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" chauffeur\\n\",\n        \"output\": \" chauffeur does not have SELFIES\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C]\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Bromohexane\\n\",\n        \"output\": \" CCCCCCBr\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Br]\\n\",\n        \"output\": \" 0.003715352290971724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Octene \\n\",\n        \"output\": \" CCCCCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Lactose\\n\",\n        \"output\": \" [O][C][C][O][C][Branch2][Ring1][Branch1][O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][O][C][Ring1][=Branch2][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Ring2][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H7NO/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2\\n\",\n        \"output\": \" p-Aminophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\\n\",\n        \"output\": \" Chlortoluron\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" Propylcyclopentane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Propiconazole\\n\",\n        \"output\": \" [C][C][C][C][C][O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][Ring2][O][Ring1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc2cnc1cncnc1n2\\n\",\n        \"output\": \" 7-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" c1cc2ccc3ccc4ccc5cccc6c(c1)c2c3c4c56\\n\",\n        \"output\": \" 9.594006315159356e-10 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 1-Decene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Trichloroethylene\\n\",\n        \"output\": \" InChI=1S/C2HCl3/c3-1-2(4)5/h1H\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][NH1][C][=Ring1][Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" Theophylline\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Toluene \\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Butanone\\n\",\n        \"output\": \" InChI=1S/C4H8O/c1-3-4(2)5/h3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][Branch2][Ring1][=Branch1][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][Branch2][=O]\\n\",\n        \"output\": \" Atovaquone(0,430mg/ml) - neutral\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C19H14F3NO/c1-23-11-16(13-6-3-2-4-7-13)18(24)17(12-23)14-8-5-9-15(10-14)19(20,21)22/h2-12H,1H3\\n\",\n        \"output\": \" 3.58921934645005e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(=O)OCC(COC(=O)C)OC(=O)C\\n\",\n        \"output\": \" 0.251188643150958 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H5Cl/c7-6-4-2-1-3-5-6/h1-5H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H11ClN2O/c1-12(2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\\n\",\n        \"output\": \" Monuron\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" COc1ccc(NC(=O)N(C)C)cc1Cl\\n\",\n        \"output\": \" 0.0027289777828080433 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-3-4(5)6-2/h3H2,1-2H3\\n\",\n        \"output\": \" 0.72443596007499 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1ccccc1C\\n\",\n        \"output\": \" o-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Oxycarboxin\\n\",\n        \"output\": \" CC1=C(C(=O)Nc2ccccc2)S(=O)(=O)CCO1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][=Branch2][C][Branch1][C][O][C][Ring1][=Branch1][O][N][C][=N][C][=C][Branch1][C][O][N][=C][N][=C][Ring1][#Branch2][Ring1][#Branch1]\\n\",\n        \"output\": \" Inosine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 5-Ethyl-5-phenylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" Diethyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C19H14/c1-13-12-19-16-8-3-2-6-14(16)10-11-18(19)17-9-5-4-7-15(13)17/h2-12H,1H3\\n\",\n        \"output\": \" 2.691534803926914e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Nc1nc[nH]n1\\n\",\n        \"output\": \" 3.326595532940045 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2,4,5-Tetrachlorobenzene\\n\",\n        \"output\": \" InChI=1S/C6H2Cl4/c7-3-1-4(8)6(10)2-5(3)9/h1-2H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][S]\\n\",\n        \"output\": \" Butanethiol \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl\\n\",\n        \"output\": \" 1.148153621496884e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc1ccccc1OCC(O)COC(N)=O\\n\",\n        \"output\": \" Methocarbamol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" OC(C(=O)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" benzoin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-Methylbiphenyl\\n\",\n        \"output\": \" InChI=1S/C13H12/c1-11-7-9-13(10-8-11)12-5-3-2-4-6-12/h2-10H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ethyl-p-aminobenzoate\\n\",\n        \"output\": \" InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C15H14F3N3O4S2/c16-15(17,18)10-7-11-13(8-12(10)26(19,22)23)27(24,25)21-14(20-11)6-9-4-2-1-3-5-9/h1-5,7-8,14,20-21H,6H2,(H2,19,22,23)\\n\",\n        \"output\": \" -3.59\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Phthalonitrile\\n\",\n        \"output\": \" N#Cc1ccccc1C#N\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3\\n\",\n        \"output\": \" 0.06165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\\n\",\n        \"output\": \" Maltose\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,4-Benzenediol\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Isoquinoline\\n\",\n        \"output\": \" 0.03548133892335755 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" ClCBr\\n\",\n        \"output\": \" -0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)CC(=O)C\\n\",\n        \"output\": \" -0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chlortoluron\\n\",\n        \"output\": \" InChI=1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H5NO/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)\\n\",\n        \"output\": \" 2-Hydroxypyridine\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Pyrazinamide\\n\",\n        \"output\": \" -0.667\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCSC(=O)N(CC(C)C)CC(C)C\\n\",\n        \"output\": \" Butylate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" Cyclohexene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Pyrimidine\\n\",\n        \"output\": \" [C][=C][N][=C][N][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" m-Fluorobromobenzene\\n\",\n        \"output\": \" Fc1cccc(Br)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C4H10S/c1-2-3-4-5/h5H,2-4H2,1H3\\n\",\n        \"output\": \" -2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\",\n        \"output\": \" -3.785\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Ethylbutanal\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][O][C][=C]\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2,3-Dimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Isonazid\\n\",\n        \"output\": \" InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][C][C][O][C][Branch1][Ring1][C][O][Branch2][Ring2][#Branch2][O][C][O][C][Branch2][Ring1][=Branch1][C][O][C][O][C][Branch1][Ring1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Branch1][O][C][Branch1][C][O][C][Ring2][Ring1][#C][O]\\n\",\n        \"output\": \" 0.3890451449942806 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3\\n\",\n        \"output\": \" -4.02\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2\\n\",\n        \"output\": \" 6.606934480075964e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H4BrF/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" m-Fluorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][Ring1][C][#C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.00012589254117941674 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][P][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][Cl][=C][Ring1][P]\\n\",\n        \"output\": \" 3.467368504525317e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(=O)Nc1ccccc1\\n\",\n        \"output\": \" Acetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" C1CCc2ccccc2C1\\n\",\n        \"output\": \" -4.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCNc1nc(NC(C)(C)C)nc(SC)n1\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Progesterone\\n\",\n        \"output\": \" CC(=O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 3-Hexanol\\n\",\n        \"output\": \" CCCC(O)CC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3\\n\",\n        \"output\": \" Caproaldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" DDD\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,1-Diethoxyethane \\n\",\n        \"output\": \" InChI=1S/C6H14O2/c1-4-7-6(3)8-5-2/h6H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 4-Methyl-2-pentanol\\n\",\n        \"output\": \" 0.15848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Benzotriazole\\n\",\n        \"output\": \" c2ccc1[nH]nnc1c2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H6O2/c1-3-4(5)6-2/h3H,1H2,2H3\\n\",\n        \"output\": \" Methyl acrylate\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCCC\\n\",\n        \"output\": \" Nonane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H5NO3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)\\n\",\n        \"output\": \" -3.6039999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 5,6-Dimethylchrysene\\n\",\n        \"output\": \" Cc1c(C)c2c3ccccc3ccc2c4ccccc14\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 1-Chloro-2-methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Hexane \\n\",\n        \"output\": \" [C][C][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" t-Pentylbenzene\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][I]\\n\",\n        \"output\": \" 0.025118864315095794 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H14NO5P/c1-6(5-7(9)8-2)13-14(10,11-3)12-4/h5H,1-4H3,(H,8,9)\\n\",\n        \"output\": \" 4.477133041763624 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccc(O)cc1\\n\",\n        \"output\": \" 1,4-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CN(C)C(=O)Nc1cccc(c1)C(F)(F)F\\n\",\n        \"output\": \" -3.32\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,5-Hexadiene \\n\",\n        \"output\": \" [C][=C][C][C][C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1,1-Diethoxyethane \\n\",\n        \"output\": \" 0.37153522909717257 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Triadimefon\\n\",\n        \"output\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=N][C][=N][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" difluron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Brc1cc(Br)c(Br)cc1Br\\n\",\n        \"output\": \" -6.98\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCC=O\\n\",\n        \"output\": \" Valeraldehyde\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,4-Difluorobenzene\\n\",\n        \"output\": \" Fc1ccc(F)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1,1,2-Trichloroethane\\n\",\n        \"output\": \" -1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C9H17N5O/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" 0.008241381150130022 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Fenfuram\\n\",\n        \"output\": \" Cc1occc1C(=O)Nc2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C11H15NO3/c1-8(2)14-9-6-4-5-7-10(9)15-11(13)12-3/h4-8H,1-3H3,(H,12,13)\\n\",\n        \"output\": \" 0.008912509381337459 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" Ethyl hexanoate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H18/c1-4-5-6-7-8(2)3/h8H,4-7H2,1-3H3\\n\",\n        \"output\": \" 2-Methylheptane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCCC(C)CO\\n\",\n        \"output\": \" 0.07762471166286916 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Nitroaniline\\n\",\n        \"output\": \" Nc1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 4-Chlorotoluene\\n\",\n        \"output\": \" -3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)CCC)CC=C\\n\",\n        \"output\": \" Secobarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 0.33884415613920255 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" chloropropylate\\n\",\n        \"output\": \" c1ccc(Cl)cc1C(c2ccc(Cl)cc2)(O)C(=O)OC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=N(=O)c1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" 1,4-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][S][C][=Branch1][C][=S][N][C][Ring1][=Branch1][=O]\\n\",\n        \"output\": \" -1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H5BrO/c7-5-1-3-6(8)4-2-5/h1-4,8H\\n\",\n        \"output\": \" -1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][I]\\n\",\n        \"output\": \" -4.81\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C]\\n\",\n        \"output\": \" 5,5-Dimethylbarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H9Cl/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H\\n\",\n        \"output\": \" 2-Chlorobiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propiconazole\\n\",\n        \"output\": \" CCCC1COC(Cn2cncn2)(O1)c3ccc(Cl)cc3Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)SCCSCC\\n\",\n        \"output\": \" Disulfoton\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H9Cl/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H\\n\",\n        \"output\": \" -4.88\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)SC4CC1=CC(=O)CCC1(C)C5CCC2(C)C(CCC23CCC(=O)O3)C45\\n\",\n        \"output\": \" -4.173\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 5,6-Dimethylchrysene\\n\",\n        \"output\": \" 9.772372209558111e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" m-Chloronitrobenzene \\n\",\n        \"output\": \" Clc1cccc(c1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1,2-Dibromobenzene\\n\",\n        \"output\": \" Brc1ccccc1Br\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" -6.18\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 4-Chlorophenol \\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCBr\\n\",\n        \"output\": \" 0.0812830516164099 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" C/C=C/C=O\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3\\n\",\n        \"output\": \" p-Cresol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Methyl-2-butanone\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Benzophenone\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Methazole\\n\",\n        \"output\": \" InChI=1S/C9H6Cl2N2O3/c1-12-8(14)13(16-9(12)15)5-2-3-6(10)7(11)4-5/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][=C][=C][C][Branch1][=Branch1][N][=Branch1][C][=O][=O][=C][Ring1][=Branch2][O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" DNOC\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C(=O)C(C)C\\n\",\n        \"output\": \" 2,4-Dimethyl-3-pentanone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Fluridone\\n\",\n        \"output\": \" 3.58921934645005e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2\\n\",\n        \"output\": \" Cyhalothrin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1-Chloronapthalene\\n\",\n        \"output\": \" Clc1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Chloropropane\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67\\n\",\n        \"output\": \" -9.332\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" BrC(Cl)Cl\\n\",\n        \"output\": \" -1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" m-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,3,4,5-Tetrachlorophenol\\n\",\n        \"output\": \" [O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][=Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][C][Br]\\n\",\n        \"output\": \" 1-Chloro-2-bromoethane\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C15H12N2O2/c18-13-15(17-14(19)16-13,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H2,16,17,18,19)\\n\",\n        \"output\": \" -4.0969999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Benznidazole\\n\",\n        \"output\": \" -2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benznidazole\\n\",\n        \"output\": \" InChI=1S/C12H12N4O3/c17-11(14-8-10-4-2-1-3-5-10)9-15-7-6-13-12(15)16(18)19/h1-7H,8-9H2,(H,14,17)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C15H11N3O3/c19-14-9-16-15(10-4-2-1-3-5-10)12-8-11(18(20)21)6-7-13(12)17-14/h1-8H,9H2,(H,17,19)\\n\",\n        \"output\": \" 0.0001599558028614668 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Lactose\\n\",\n        \"output\": \" InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Tetradecane\\n\",\n        \"output\": \" CCCCCCCCCCCCCC\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCS\\n\",\n        \"output\": \" Ethanethiol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccccc1O\\n\",\n        \"output\": \" 1,2-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Isopentyl acetate\\n\",\n        \"output\": \" CC(C)CCOC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Deoxycorticosterone\\n\",\n        \"output\": \" CC12CCC3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3,3-Dimethyl-2-butanone\\n\",\n        \"output\": \" CC(=O)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N]\\n\",\n        \"output\": \" -3.536\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccc2c(c1)c3cccc4ccc5cccc2c5c43\\n\",\n        \"output\": \" Benzo(e)pyrene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][Branch1][C][C][S][C][C][S][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C]\\n\",\n        \"output\": \" 13.931568029453036 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Methoxychlor\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Methyl decanoate\\n\",\n        \"output\": \" 2.0417379446695274e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" citral\\n\",\n        \"output\": \" CC(C)=CCCC(C)=CC(=O)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Iodoheptane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][I]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Phoxim\\n\",\n        \"output\": \" -4.862\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\\n\",\n        \"output\": \" -6.9\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 2,4-Dinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H12/c1-7-5-3-2-4-6-7/h5H,2-4,6H2,1H3\\n\",\n        \"output\": \" 1-Methylcyclohexene \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][=C][N][Branch1][=N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 5.000345349769783e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][O][Ring1][Ring1]\\n\",\n        \"output\": \" 0.2570395782768864 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCc1ccccc1\\n\",\n        \"output\": \" Hexylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc2c(c1)cc3ccc4cccc5ccc2c3c45\\n\",\n        \"output\": \" 1.9998618696327446e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Ethyl decanoate\\n\",\n        \"output\": \" CCCCCCCCCC(=O)OCC\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-methoxypteridine\\n\",\n        \"output\": \" COc2ncc1nccnc1n2\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-benzidine\\n\",\n        \"output\": \" InChI=1S/C12H12N2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H,13-14H2\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Pirimicarb\\n\",\n        \"output\": \" InChI=1S/C11H18N4O2/c1-7-8(2)12-10(14(3)4)13-9(7)17-11(16)15(5)6/h1-6H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Brc1cc(Br)c(Br)cc1Br\\n\",\n        \"output\": \" 1,2,4,5-Tetrabromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 1-Chloroheptane\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 4-methylpteridine\\n\",\n        \"output\": \" -0.466\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Trietazine\\n\",\n        \"output\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-3-4-8(9)5-7(6)2/h3-5,9H,1-2H3\\n\",\n        \"output\": \" -1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCC=C\\n\",\n        \"output\": \" 0.0005888436553555889 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Diisopropylsulfide\\n\",\n        \"output\": \" [C][C][Branch1][C][C][S][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" OCC1OC(O)(CO)C(O)C1O\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCOP(=S)(OCC)N2C(=O)c1ccccc1C2=O\\n\",\n        \"output\": \" Ditalimfos\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Amitrole\\n\",\n        \"output\": \" [N][C][N][=C][NH1][N][=Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Cyclooctyl-5-spirobarbituric acid\\n\",\n        \"output\": \" InChI=1S/C11H16N2O3/c14-8-11(9(15)13-10(16)12-8)6-4-2-1-3-5-7-11/h1-7H2,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Isopropyl acetate\\n\",\n        \"output\": \" CC(C)OC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methyl acrylate\\n\",\n        \"output\": \" COC(=O)C=C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,4,6-Trichlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H3Cl3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Dioxacarb\\n\",\n        \"output\": \" [C][N][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][C][O][Ring1][Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chrysene\\n\",\n        \"output\": \" InChI=1S/C18H12/c1-3-7-15-13(5-1)9-11-18-16-8-4-2-6-14(16)10-12-17(15)18/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Tricresyl phosphate\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch2][Ring1][=C][O][P][=Branch1][C][=O][Branch1][=N][O][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][Ring2][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C20H20N2O4/c1-2-9-17(23)26-14-22-18(24)20(21-19(22)25,15-10-5-3-6-11-15)16-12-7-4-8-13-16/h3-8,10-13H,2,9,14H2,1H3,(H,21,25)\\n\",\n        \"output\": \" 3-Butanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCC(C)(C)CO\\n\",\n        \"output\": \" 0.09120108393559097 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl][C][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.007744617978025192 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H9N/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-9H\\n\",\n        \"output\": \" Acridine\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" O=C(Cn1ccnc1N(=O)=O)NCc2ccccc2\\n\",\n        \"output\": \" -2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Phenol\\n\",\n        \"output\": \" 1.0 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Methylfluorene\\n\",\n        \"output\": \" Cc1cccc2c1Cc3ccccc32\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Chlorbromuron\\n\",\n        \"output\": \" [C][O][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Br][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,6-Dimethylpyridine\\n\",\n        \"output\": \" Cc1cccc(C)n1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" O-Ethyl carbamate\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][N]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" NC(=O)c1ccccc1O\\n\",\n        \"output\": \" 0.01458814260275349 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Dimefuron\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2,6-Dichlorophenol\\n\",\n        \"output\": \" [O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][S][=C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" Equilin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][N][C][C][=N][N][Branch2][Ring1][Ring1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][=Ring1][P][Cl]\\n\",\n        \"output\": \" 8.994975815300346e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Phenacetin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" XMC\\n\",\n        \"output\": \" CNC(=O)Oc1cc(C)cc(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Trichlorfon\\n\",\n        \"output\": \" COP(=O)(OC)C(O)C(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H\\n\",\n        \"output\": \" 0.002818382931264455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 6-methoxypteridine\\n\",\n        \"output\": \" -1.139\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cyclopentyl-5-spirobarbituric acid\\n\",\n        \"output\": \" O=C2NC(=O)C1(CCCC1)C(=O)N2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H17ClNO4PS2/c1-3-19-21(22,20-4-2)23-12(9-15)16-13(17)10-7-5-6-8-11(10)14(16)18/h5-8,12H,3-4,9H2,1-2H3\\n\",\n        \"output\": \" Dialifor\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dienochlor\\n\",\n        \"output\": \" ClC1=C(Cl)C(Cl)(C(=C1Cl)Cl)C2(Cl)C(=C(Cl)C(=C2Cl)Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" -1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-5-6-7(2,3)8/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" 2-Methyl-2-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C22H28F2O5/c1-11-6-13-14-8-16(23)15-7-12(26)4-5-19(15,2)21(14,24)17(27)9-20(13,3)22(11,29)18(28)10-25/h4-5,7,11,13-14,16-17,25,27,29H,6,8-10H2,1-3H3\\n\",\n        \"output\": \" 2.437810818368755e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Pentanone\\n\",\n        \"output\": \" InChI=1S/C5H10O/c1-3-5(6)4-2/h3-4H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fructose\\n\",\n        \"output\": \" [O][C][C][O][C][Branch1][C][O][Branch1][Ring1][C][O][C][Branch1][C][O][C][Ring1][=Branch2][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Raffinose\\n\",\n        \"output\": \" OCC1OC(CO)(OC2OC(COC3OC(CO)C(O)C(O)C3O)C(O)C(O)C2O)C(O)C1O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" C1N(C(=O)NCC(C)C)C(=O)NC1\\n\",\n        \"output\": \" isocarbamid\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Norethisterone\\n\",\n        \"output\": \" InChI=1S/C20H26O3/c1-3-19(22)10-8-16-15-5-4-13-12-14(21)6-11-20(13,23)17(15)7-9-18(16,19)2/h1,12,15-17,22-23H,4-11H2,2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-6(4-2)5-7/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC/C=C/C\\n\",\n        \"output\": \" 0.0028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 4-Nitroacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCC(CC)CO\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C23H19ClF3NO3/c1-22(2)17(12-19(24)23(25,26)27)20(22)21(29)31-18(13-28)14-7-6-10-16(11-14)30-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\",\n        \"output\": \" 6.668067692136219e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Anisole\\n\",\n        \"output\": \" InChI=1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" o1c2ccccc2c3ccccc13\\n\",\n        \"output\": \" Dibenzofurane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3\\n\",\n        \"output\": \" 0.0005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H4N2/c9-5-7-3-1-2-4-8(7)6-10/h1-4H\\n\",\n        \"output\": \" 0.004168693834703355 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][O][C][=N][C][=Branch1][#Branch2][=N][C][Branch1][C][C][=C][Ring1][#Branch1][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" Pirimicarb\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Benzophenone\\n\",\n        \"output\": \" [O][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Hexanol\\n\",\n        \"output\": \" [C][C][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Pentanone\\n\",\n        \"output\": \" CCCC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=C2NC(=O)C1(CCCCCCC1)C(=O)N2\\n\",\n        \"output\": \" Cyclooctyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Chlorophenol\\n\",\n        \"output\": \" InChI=1S/C6H5ClO/c7-5-2-1-3-6(8)4-5/h1-4,8H\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][/C][=C][/C][=O]\\n\",\n        \"output\": \" 2.0892961308540396 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" benodanil\\n\",\n        \"output\": \" [C][=C][Branch1][#C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][I][C][=C][C][=C][Ring1][S]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,4-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.02187761623949553 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2,3',4',5-PCB\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][=N]\\n\",\n        \"output\": \" Terbumeton\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc1ccc(cc1)S(=O)(=O)c2ccc(N)cc2\\n\",\n        \"output\": \" Dapsone\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 5-Allyl-5-methylbarbital\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Camphor\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Nitramine\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Prometon\\n\",\n        \"output\": \" COc1nc(NC(C)C)nc(NC(C)C)n1\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CC(C)O\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#C][C][Ring1][=Branch1][=C][Ring1][#Branch2][Ring1][=C]\\n\",\n        \"output\": \" Benzo(e)pyrene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,4-Dimethyl-3-pentanol\\n\",\n        \"output\": \" CC(C)C(O)C(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][O][C][=O]\\n\",\n        \"output\": \" -1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCCCCCCCCCCCO\\n\",\n        \"output\": \" 1-Octadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Nitronapthalene\\n\",\n        \"output\": \" 0.00028840315031266055 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Hydroxypyridine\\n\",\n        \"output\": \" InChI=1S/C5H5NO/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" meconin\\n\",\n        \"output\": \" [C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][C][=Branch1][C][=O][O][C][C][Ring1][=Branch1][C][=Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Sparsomycin (3,8mg/ml)\\n\",\n        \"output\": \" 0.010447202192208004 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C13H14F3N3O4/c1-4-17(7-8(2)3)12-10(18(20)21)5-9(13(14,15)16)6-11(12)19(22)23/h5-6H,2,4,7H2,1,3H3\\n\",\n        \"output\": \" 7.516228940182061e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.012022644346174132 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][C][O]\\n\",\n        \"output\": \" 0.07762471166286916 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethyl-p-hydroxybenzoate \\n\",\n        \"output\": \" CCOC(=O)c1ccc(O)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Ring1][=C]\\n\",\n        \"output\": \" 1.2882495516931348e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" p-benzidine\\n\",\n        \"output\": \" Nc1ccc(cc1)c2ccc(N)cc2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC(Cl)(Cl)N(=O)=O\\n\",\n        \"output\": \" Chloropicrin\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=O]\\n\",\n        \"output\": \" Methyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3\\n\",\n        \"output\": \" Phenetole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Diphenyl ether \\n\",\n        \"output\": \" InChI=1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 3-Propanoyloxymethylphenytoin\\n\",\n        \"output\": \" O=C1N(COC(=O)CC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methaqualone\\n\",\n        \"output\": \" InChI=1S/C16H14N2O/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19/h3-10H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [Cl][C][Branch2][Ring1][=C][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Branch1][C][Cl][C][Ring1][#Branch2][Branch1][C][Cl][C][Ring1][=Branch2][Branch1][C][Cl][Cl][C][Ring1][Branch2][Branch1][C][Cl][C][Branch1][C][Cl][Branch1][C][Cl][C][Ring2][Ring1][Ring1][Ring1][#C][Cl]\\n\",\n        \"output\": \" 1.584893192461114e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 4-Chlorotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Deltamethrin\\n\",\n        \"output\": \" InChI=1S/C22H19Br2NO3/c1-22(2)17(12-19(23)24)20(22)21(26)28-18(13-25)14-7-6-10-16(11-14)27-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H12O4/c1-3-10-6(8)5-7(9)11-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" Malonic acid diethylester\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" Propyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 1,3-Dimethylnaphthalene\\n\",\n        \"output\": \" InChI=1S/C12H12/c1-9-7-10(2)12-6-4-3-5-11(12)8-9/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H10O/c1-6-3-4-8(9)7(2)5-6/h3-5,9H,1-2H3\\n\",\n        \"output\": \" -1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C20H12/c1-2-7-17-15(4-1)12-16-9-8-13-5-3-6-14-10-11-18(17)20(16)19(13)14/h1-12H\\n\",\n        \"output\": \" 1.9998618696327446e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCC(=C)C\\n\",\n        \"output\": \" 2-Methyl-1-Pentene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,3-Dimethyl-1,3-Butadiene\\n\",\n        \"output\": \" InChI=1S/C6H10/c1-5(2)6(3)4/h1,3H2,2,4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Chlorobutane\\n\",\n        \"output\": \" -1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H8O/c1-2-4-5-3-1/h1-4H2\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H7Cl/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H\\n\",\n        \"output\": \" 2-Chloronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][O][C][C][C]\\n\",\n        \"output\": \" 0.023988329190194897 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Tetrahydropyran \\n\",\n        \"output\": \" [C][C][C][O][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C12H11NO2/c1-9-11(7-8-15-9)12(14)13-10-5-3-2-4-6-10/h2-8H,1H3,(H,13,14)\\n\",\n        \"output\": \" -3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Isocarboxazid\\n\",\n        \"output\": \" InChI=1S/C12H13N3O2/c1-9-7-11(15-17-9)12(16)14-13-8-10-5-3-2-4-6-10/h2-7,13H,8H2,1H3,(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" p-Phenylphenol\\n\",\n        \"output\": \" 0.0003311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Dieldrin\\n\",\n        \"output\": \" 5.128613839913648e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CN(C)C(=O)Oc1nc(nc(C)c1C)N(C)C\\n\",\n        \"output\": \" 0.011220184543019636 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCBr\\n\",\n        \"output\": \" -2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Chlorthalidone\\n\",\n        \"output\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Stirofos\\n\",\n        \"output\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][=Branch1][Ring1][=C][Cl][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H10Cl2N2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)\\n\",\n        \"output\": \" Linuron\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" ethofumesate\\n\",\n        \"output\": \" 0.00038018939632056124 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Decanone\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Undecanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Chlorodibromethane\\n\",\n        \"output\": \" -1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCCCCCCBr\\n\",\n        \"output\": \" -5.06\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Prasterone\\n\",\n        \"output\": \" [C][C][C][C][C][C][Branch1][P][C][C][=C][C][C][Branch1][C][O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Methyl-2-pentanol\\n\",\n        \"output\": \" CCCC(C)(C)O\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCC(CC)CO\\n\",\n        \"output\": \" 2-Ethyl-1-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=C][C]\\n\",\n        \"output\": \" 2-Methyl-1-Pentene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Hexane \\n\",\n        \"output\": \" 0.0001445439770745928 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methyl butyl ether \\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-3-4-5-6-2/h3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-5-6-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" Ethyl propyl ether\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-4-5(2)6(3)7/h5H,4H2,1-3H3\\n\",\n        \"output\": \" -0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" O=N(=O)c1cc(cc(c1)N(=O)=O)N(=O)=O\\n\",\n        \"output\": \" 0.0012882495516931337 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Trietazine\\n\",\n        \"output\": \" CCNc1nc(Cl)nc(n1)N(CC)CC\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3\\n\",\n        \"output\": \" Dexamethasone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2\\n\",\n        \"output\": \" Dapsone\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Methylpentane\\n\",\n        \"output\": \" -3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C)CC=C\\n\",\n        \"output\": \" 0.06918309709189366 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" 1,3-Dimethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Camphor\\n\",\n        \"output\": \" CC1(C)C2CCC1(C)C(=O)C2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [N][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Phenylhydrazine\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCOCCO\\n\",\n        \"output\": \" 0.3801893963205612 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3\\n\",\n        \"output\": \" 0.00010023052380779004 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Hexanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-3-5-6(7)4-2/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 0.00044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][N][C][=Branch1][C][=S][N][C][C]\\n\",\n        \"output\": \" 0.034673685045253165 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H19NO3/c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15/h2-3,6-9,12H,1,4-5,10-11,13H2\\n\",\n        \"output\": \" Piperine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Chlorotoluron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 6-methoxypteridine\\n\",\n        \"output\": \" InChI=1S/C7H6N4O/c1-12-6-3-9-7-5(11-6)2-8-4-10-7/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][O][=O]\\n\",\n        \"output\": \" Coumachlor\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][O][C][=O]\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" N,N-Dimethylacetamide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=N][C][=N][Ring1][Branch1]\\n\",\n        \"output\": \" Triadimefon\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Etomidate\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][=C][N][=C][N][Ring1][Branch1][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCN(CC)c1ccccc1\\n\",\n        \"output\": \" 0.0009332543007969915 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Br]\\n\",\n        \"output\": \" 8.709635899560814e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Terbufos\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][S][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cyclohexyl-5-spirobarbituric acid\\n\",\n        \"output\": \" O=C2NC(=O)C1(CCCCC1)C(=O)N2\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" chlordimeform\\n\",\n        \"output\": \" 0.0013803842646028853 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc1ccc(cc1)S(N)(=O)=O\\n\",\n        \"output\": \" Sulfanilamide\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3,4-Dimethylpyridine\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-3-4-8-5-7(6)2/h3-5H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its oil solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][=C][C][Ring1][Branch1]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Nc1ccccc1\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2-Dichlorotetrafluoroethane\\n\",\n        \"output\": \" FC(F)(Cl)C(F)(F)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Antipyrene\\n\",\n        \"output\": \" [C][C][=C][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][N][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCCOC(=O)CCCCCCCCC(=O)OCCCC\\n\",\n        \"output\": \" 0.00012705741052085407 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCC(=O)CC\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Tetrabromomethane\\n\",\n        \"output\": \" [Br][C][Branch1][C][Br][Branch1][C][Br][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Pentamethylbenzene\\n\",\n        \"output\": \" [C][C][=C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][=Branch2][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Ethylbenzene\\n\",\n        \"output\": \" CCc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Anisole\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)CC(c1ccc(Cl)cc1)c2c(O)c3ccccc3oc2=O\\n\",\n        \"output\": \" 1.4487718535447632e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCBr\\n\",\n        \"output\": \" 0.0001548816618912481 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Siduron\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Dimefuron\\n\",\n        \"output\": \" CN(C)C(=O)Nc1ccc(c(Cl)c1)n2nc(oc2=O)C(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" allicin\\n\",\n        \"output\": \" InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" Cypermethrin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 2-Ethyltoluene\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Procymidone\\n\",\n        \"output\": \" InChI=1S/C13H11Cl2NO2/c1-12-6-13(12,2)11(18)16(10(12)17)9-4-7(14)3-8(15)5-9/h3-5H,6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCC(Br)(CC)C(=O)NC(N)=O\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Lorazepam\\n\",\n        \"output\": \" InChI=1S/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)C\\n\",\n        \"output\": \" 2-Methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" description\\n\",\n        \"output\": \" description does not have SELFIES\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H9Cl/c1-2-3-4-5/h2-4H2,1H3\\n\",\n        \"output\": \" 0.009332543007969915 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccc2c(c1)c3cccc4c3c2cc5ccccc54\\n\",\n        \"output\": \" -8.23\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.20892961308540392 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 3-Methylcholanthrene\\n\",\n        \"output\": \" -7.92\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Chloroiodobenzene\\n\",\n        \"output\": \" InChI=1S/C6H4ClI/c7-5-1-3-6(8)4-2-5/h1-4H\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dichloromethane\\n\",\n        \"output\": \" InChI=1S/CH2Cl2/c2-1-3/h1H2\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Coumaphos\\n\",\n        \"output\": \" CCOP(=S)(OCC)Oc2ccc1oc(=O)c(Cl)c(C)c1c2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CBr\\n\",\n        \"output\": \" Bromomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 0.436515832240166 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Risocaine\\n\",\n        \"output\": \" [C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Nitronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)CCCO\\n\",\n        \"output\": \" 4-Methylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CN2C(=O)CN=C(c1ccccc1)c3cc(Cl)ccc23\\n\",\n        \"output\": \" 0.0001761976046411631 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(C)(O)CC\\n\",\n        \"output\": \" 3-Methyl-3-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/CH2Br2/c2-1-3/h1H2\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1-Napthol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12N2O2/c1-2-13-8-5-3-7(4-6-8)11-9(10)12/h3-6H,2H2,1H3,(H3,10,11,12)\\n\",\n        \"output\": \" Dulcin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Clc1cccc(Cl)c1\\n\",\n        \"output\": \" 1,3-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2,4,5-Trichlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=C(Nc1ccccc1)Nc2ccccc2\\n\",\n        \"output\": \" 0.000707945784384138 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][=N]\\n\",\n        \"output\": \" Terbutryn\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)CCC(C)C\\n\",\n        \"output\": \" 5-Ethyl-5-(3-methylbutyl)barbital\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2-Decanone\\n\",\n        \"output\": \" 0.0005011872336272725 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H12O4/c1-3-10-6(8)5-7(9)11-4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" 0.15135612484362082 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CC(=C)C=C\\n\",\n        \"output\": \" 0.009332543007969915 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][Branch1][Branch2][C][O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.47\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Ethyl pyridine\\n\",\n        \"output\": \" 3.2359365692962827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" diisooctyl phthalate\\n\",\n        \"output\": \" InChI=1S/C24H38O4/c1-19(2)13-7-5-11-17-27-23(25)21-15-9-10-16-22(21)24(26)28-18-12-6-8-14-20(3)4/h9-10,15-16,19-20H,5-8,11-14,17-18H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" Methyl propyl ether \\n\",\n        \"output\": \" 0.40738027780411273 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C6H6N2O2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H,7H2\\n\",\n        \"output\": \" 0.004265795188015926 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Dibromomethane\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][#N]\\n\",\n        \"output\": \" Propionitrile\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Propyl acetate\\n\",\n        \"output\": \" CCCOC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Ethyl formate\\n\",\n        \"output\": \" [C][C][O][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCOC(=O)C\\n\",\n        \"output\": \" Pentyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][O]\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1cc(C)c(C)c(C)c1C\\n\",\n        \"output\": \" -4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H7NO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" 1-Nitronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Chlorotoluene\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Methyl formate\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\\n\",\n        \"output\": \" Fluorometuron\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12/c1-3-9-7-5-4-6-8(9)2/h4-7H,3H2,1-2H3\\n\",\n        \"output\": \" 2-Ethyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 1.584893192461114e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" cactus\\n\",\n        \"output\": \" cactus does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" N(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Diphenylamine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3\\n\",\n        \"output\": \" Etoposide (148-167,25mg/ml)\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Branch2][C][Branch1][C][C][C][C][C][C][C][=C]\\n\",\n        \"output\": \" 0.0044055486350655345 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" BrCCBr\\n\",\n        \"output\": \" 1,2-Dibromoethane\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][O][C][C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][S][C][=N][Ring1][N]\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][S][S][C]\\n\",\n        \"output\": \" -1.44\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 6.456542290346549e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" o-Nitroaniline\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][Branch1][C][C][=C][C][C][C][Branch1][C][C][=C][C][=O]\\n\",\n        \"output\": \" -2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2-Diethoxyethane \\n\",\n        \"output\": \" InChI=1S/C6H14O2/c1-3-7-5-6-8-4-2/h3-6H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" p-Methoxybenzaldehyde\\n\",\n        \"output\": \" 0.03235936569296283 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" Nitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Fluvalinate\\n\",\n        \"output\": \" InChI=1S/C26H22ClF3N2O3/c1-16(2)24(32-22-12-11-18(14-21(22)27)26(28,29)30)25(33)35-23(15-31)17-7-6-10-20(13-17)34-19-8-4-3-5-9-19/h3-14,16,23-24,32H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C19H14/c1-13-12-15-7-3-4-8-16(15)18-11-10-14-6-2-5-9-17(14)19(13)18/h2-12H,1H3\\n\",\n        \"output\": \" 5-Methylchrysene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlorodibromethane\\n\",\n        \"output\": \" ClC(Br)Br\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methylparaben\\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethyl pentanoate\\n\",\n        \"output\": \" [C][C][C][O][C][=Branch1][C][=O][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][C][Branch1][#C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][Branch2][=O][C][=C][C][C][C][C][C][Ring1][#Branch1][C][Ring1][Branch1]\\n\",\n        \"output\": \" Reposal\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][#Branch2][C][C][C][C][C][C][C][Ring1][Branch2][C][=Branch1][C][=O][N][Ring1][#C]\\n\",\n        \"output\": \" Cyclooctyl-5-spirobarbituric acid\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in room temperature. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][Branch1][Ring1][C][C][C][C]\\n\",\n        \"output\": \" 8.709635899560814e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1cc(C)cc(O)c1\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Raffinose\\n\",\n        \"output\": \" [O][C][C][O][C][Branch1][Ring1][C][O][Branch2][Ring2][#Branch2][O][C][O][C][Branch2][Ring1][=Branch1][C][O][C][O][C][Branch1][Ring1][C][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring1][#Branch2][O][C][Branch1][C][O][C][Branch1][C][O][C][Ring2][Ring1][Branch1][O][C][Branch1][C][O][C][Ring2][Ring1][#C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H\\n\",\n        \"output\": \" 0.1096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C16H18N2O3/c1-18(2)16(19)17-12-4-6-14(7-5-12)21-15-10-8-13(20-3)9-11-15/h4-11H,1-3H3,(H,17,19)\\n\",\n        \"output\": \" -4.16\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H8Cl6/c13-8-9(14)11(16)7-5-2-1-4(3-5)6(7)10(8,15)12(11,17)18/h1-2,4-7H,3H2\\n\",\n        \"output\": \" 4.931738039549355e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C14H8Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8H\\n\",\n        \"output\": \" DDE\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCc1ccccc1C\\n\",\n        \"output\": \" 2-Ethyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Nitrophenol\\n\",\n        \"output\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" c1ccc2c(c1)[nH]c3ccccc32\\n\",\n        \"output\": \" -5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Anisole\\n\",\n        \"output\": \" COc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" 1,2-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-5(2,3)6-4/h1-4H3\\n\",\n        \"output\": \" Methyl t-butyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Fenarimol\\n\",\n        \"output\": \" [O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][=Branch2][C][=C][N][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 0.0011481536214968829 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" oryzalin\\n\",\n        \"output\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)S(N)(=O)=O)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,4-Difluorobenzene\\n\",\n        \"output\": \" [F][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Isocarboxazid\\n\",\n        \"output\": \" -2.461\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][N][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][N][S][Branch1][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.0005128613839913648 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H2\\n\",\n        \"output\": \" Styrene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Tetrafluthrin\\n\",\n        \"output\": \" [C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Branch2][Ring1][#C][C][O][C][=Branch1][C][=O][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][#Branch2][Branch1][C][C][C][C][Branch1][C][F][=C][Ring2][Ring1][=Branch2][F]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Br]\\n\",\n        \"output\": \" 1-Bromooctane\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Cc1ccnc(C)c1\\n\",\n        \"output\": \" 2.3988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Danazol\\n\",\n        \"output\": \" 3.1117163371060134e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][O][C][=O]\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 2,3-Dimethyl-1,3-Butadiene\\n\",\n        \"output\": \" CC(=C)C(=C)C\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" 1-Pentyne\\n\",\n        \"output\": \" 0.022908676527677734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Pentanol\\n\",\n        \"output\": \" 0.251188643150958 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" -3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Iodomethane\\n\",\n        \"output\": \" InChI=1S/CH3I/c1-2/h1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Lindane\\n\",\n        \"output\": \" InChI=1S/C6H6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-6H\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Nerol\\n\",\n        \"output\": \" [C][C][Branch1][C][C][=C][C][C][/C][Branch1][C][C][=C][\\\\C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Eriodictyol\\n\",\n        \"output\": \" 0.000239883291901949 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(=C)C=C\\n\",\n        \"output\": \" 2-Methyl-1,3-Butadiene \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][#Branch2][Cl]\\n\",\n        \"output\": \" 2,2',3,4,4',5',6-PCB\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C8H17Br/c1-2-3-4-5-6-7-8-9/h2-8H2,1H3\\n\",\n        \"output\": \" 8.709635899560814e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" cis 1,2-Dichloroethylene\\n\",\n        \"output\": \" InChI=1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 3-Hexanone\\n\",\n        \"output\": \" [C][C][C][C][=Branch1][C][=O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Valeraldehyde\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C3CN=C(c1ccccc1)c2cc(ccc2N3)N(=O)=O\\n\",\n        \"output\": \" Nitrazepam\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Chlorobiphenyl\\n\",\n        \"output\": \" 2.8840315031266056e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" Dimethyldisulfide\\n\",\n        \"output\": \" 0.03630780547701014 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Dichlorophen\\n\",\n        \"output\": \" -3.9530000000000003\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Cyclohexanone\\n\",\n        \"output\": \" [O][=C][C][C][C][C][C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][S][C][C][S][C][C]\\n\",\n        \"output\": \" Disulfoton\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCC(=O)Nc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" -3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CN(C)C(=O)SCCCCOc1ccccc1\\n\",\n        \"output\": \" Fenothiocarb\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H16N2O3/c1-4-6(3)10(5-2)7(13)11-9(15)12-8(10)14/h6H,4-5H2,1-3H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" Butabarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Propetamphos\\n\",\n        \"output\": \" [C][C][N][P][=Branch1][C][=S][Branch1][Ring1][O][C][O][C][=Branch1][N][=C][C][=Branch1][C][=O][O][C][Branch1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\",\n        \"output\": \" -5.68\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][=C]\\n\",\n        \"output\": \" -3.23\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][=N][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 1,2-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Pirimicarb\\n\",\n        \"output\": \" CN(C)C(=O)Oc1nc(nc(C)c1C)N(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" methylthiouracil\\n\",\n        \"output\": \" 0.0036643757464783332 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,2,4,5-Tetramethylbenzene\\n\",\n        \"output\": \" Cc1cc(C)c(C)cc1C\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Aldrin\\n\",\n        \"output\": \" InChI=1S/C12H8Cl6/c13-8-9(14)11(16)7-5-2-1-4(3-5)6(7)10(8,15)12(11,17)18/h1-2,4-7H,3H2\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 4-Pentene-1-ol\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" OCC(NC(=O)C(Cl)Cl)C(O)c1ccc(cc1)N(=O)=O\\n\",\n        \"output\": \" Chloramphenicol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Nitrotoluene\\n\",\n        \"output\": \" InChI=1S/C7H7NO2/c1-6-2-4-7(5-3-6)8(9)10/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H11Cl2NO2/c1-12-6-13(12,2)11(18)16(10(12)17)9-4-7(14)3-8(15)5-9/h3-5H,6H2,1-2H3\\n\",\n        \"output\": \" Procymidone\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Xylene \\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1,3-Benzenediol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Tetrachloromethane\\n\",\n        \"output\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][I]\\n\",\n        \"output\": \" Iodomethane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Tribromomethane\\n\",\n        \"output\": \" InChI=1S/CHBr3/c2-1(3)4/h1H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6)\\n\",\n        \"output\": \" 2-pyrrolidone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H3Cl2NO2/c7-4-2-1-3-5(6(4)8)9(10)11/h1-3H\\n\",\n        \"output\": \" 0.0003311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Tetradecanol\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][=O]\\n\",\n        \"output\": \" 0.14125375446227545 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" p-Nitrophenol\\n\",\n        \"output\": \" Oc1ccc(cc1)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Caffeine\\n\",\n        \"output\": \" [C][N][C][=N][C][N][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=N][=Ring1][#Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2-Methylpentanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-3-4-6(2)5-7/h6-7H,3-5H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCC(C)(C)O\\n\",\n        \"output\": \" 2-Methyl-2-heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Triphenylene\\n\",\n        \"output\": \" c1ccc2c(c1)c3ccccc3c4ccccc24\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" O=C1CCCN1\\n\",\n        \"output\": \" 11.748975549395297 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C(Cn1ccnc1N(=O)=O)NCc2ccccc2\\n\",\n        \"output\": \" Benznidazole\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][Ring2][Ring1][#Branch1][Branch1][C][C][C]\\n\",\n        \"output\": \" Fenpropathrin\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-2-3-6-4-5/h4H,2-3H2,1H3\\n\",\n        \"output\": \" 0.32359365692962827 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C(Nc1ccccc1)Nc2ccccc2\\n\",\n        \"output\": \" Carbanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)\\n\",\n        \"output\": \" -1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Monolinuron\\n\",\n        \"output\": \" InChI=1S/C9H11ClN2O2/c1-12(14-2)9(13)11-8-5-3-7(10)4-6-8/h3-6H,1-2H3,(H,11,13)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" OC1CCCCCCC1\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Acrolein\\n\",\n        \"output\": \" [C][=C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Nc1ccccc1Cl\\n\",\n        \"output\": \" o-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" C1CCCCCC1\\n\",\n        \"output\": \" -3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Biphenyl\\n\",\n        \"output\": \" InChI=1S/C12H10/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OCc1ccccc1\\n\",\n        \"output\": \" Phenylmethanol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Phenmedipham\\n\",\n        \"output\": \" InChI=1S/C16H16N2O4/c1-11-5-3-6-12(9-11)18-16(20)22-14-8-4-7-13(10-14)17-15(19)21-2/h3-10H,1-2H3,(H,17,19)(H,18,20)\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C12H10N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" 3.5481338923357534e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Theophylline\\n\",\n        \"output\": \" Cn1c(=O)n(C)c2nc[nH]c2c1=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Benzo(a)fluorene\\n\",\n        \"output\": \" C1c2ccccc2c3ccc4ccccc4c13\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.039810717055349734 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][Br]\\n\",\n        \"output\": \" o-Fluorobromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2,2',3,3'-PCB\\n\",\n        \"output\": \" 5.248074602497723e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,2',3,3',4,4',5,5'-PCB\\n\",\n        \"output\": \" InChI=1S/C12H2Cl8/c13-5-1-3(7(15)11(19)9(5)17)4-2-6(14)10(18)12(20)8(4)16/h1-2H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H19N5O/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" Terbumeton\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Fluorene \\n\",\n        \"output\": \" -5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Ethalfluralin\\n\",\n        \"output\": \" InChI=1S/C13H14F3N3O4/c1-4-17(7-8(2)3)12-10(18(20)21)5-9(13(14,15)16)6-11(12)19(22)23/h5-6H,2,4,7H2,1,3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Methane\\n\",\n        \"output\": \" C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,1,2-Trichlorotrifluoroethane\\n\",\n        \"output\": \" FC(F)(Cl)C(F)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2,2-Dimethylbutane\\n\",\n        \"output\": \" CCC(C)(C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,7-phenantroline\\n\",\n        \"output\": \" c1cnc2c(c1)ccc3ncccc23\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3\\n\",\n        \"output\": \" 2-Methylnapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC(=O)Nc1ccc(Br)cc1\\n\",\n        \"output\": \" p-Bromoacetanilide\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1,4-Cyclohexadiene\\n\",\n        \"output\": \" [C][C][=C][C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methocarbamol\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O][C][Branch1][C][N][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" O=Cc1ccco1\\n\",\n        \"output\": \" 0.7943282347242815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Methazole\\n\",\n        \"output\": \" -2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" pediatrician\\n\",\n        \"output\": \" pediatrician does not have solubility.\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Nerol\\n\",\n        \"output\": \" 0.0034673685045253167 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 7-methylpteridine\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" -0.8540000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H54/c1-3-5-7-9-11-13-15-17-19-21-23-25-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-26H2,1-2H3\\n\",\n        \"output\": \" hexacosane\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" p-Phenylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Pyridazine\\n\",\n        \"output\": \" [C][=C][C][=N][N][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Triamcinolone\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][O][C][Branch1][C][F][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][=C][C][Ring1][N][Ring1][#Branch1][C][C][Ring2][Ring1][C][C][C][Branch1][C][O][C][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2,2,5-Trimethylhexane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Cyhalothrin\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][Branch1][=C][C][=C][Branch1][C][Cl][C][Branch1][C][F][Branch1][C][F][F][C][Ring1][O][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Benfuracarb\\n\",\n        \"output\": \" InChI=1S/C20H30N2O5S/c1-7-25-17(23)11-12-22(14(2)3)28-21(6)19(24)26-16-10-8-9-15-13-20(4,5)27-18(15)16/h8-10,14H,7,11-13H2,1-6H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Ethyl butyrate\\n\",\n        \"output\": \" InChI=1S/C8H16O2/c1-3-5-6-7-10-8(9)4-2/h3-7H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC12CCC(CC1)C(C)(C)O2\\n\",\n        \"output\": \" 1,8-Cineole\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" o-Hydroxybenzamide\\n\",\n        \"output\": \" InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Methylpentane\\n\",\n        \"output\": \" InChI=1S/C6H14/c1-4-6(3)5-2/h6H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" CCCC(C)(C)CO\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Iodoethane\\n\",\n        \"output\": \" InChI=1S/C2H5I/c1-2-3/h2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyclooctane\\n\",\n        \"output\": \" InChI=1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Dicofol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H4N2O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H\\n\",\n        \"output\": \" 1,3-Dinitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21ClN2O/c20-16-12-10-15(11-13-16)14-22(18-8-4-5-9-18)19(23)21-17-6-2-1-3-7-17/h1-3,6-7,10-13,18H,4-5,8-9,14H2,(H,21,23)\\n\",\n        \"output\": \" Pencycuron\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H16O2/c1-3-5-6-7-10-8(9)4-2/h3-7H2,1-2H3\\n\",\n        \"output\": \" 0.05248074602497726 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Cc1cc(=O)n(c2ccccc2)n1C\\n\",\n        \"output\": \" Antipyrene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3\\n\",\n        \"output\": \" Dibutyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1ccc2ccccc2c1\\n\",\n        \"output\": \" 2-Chloronapthalene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2\\n\",\n        \"output\": \" Cyclohexanol \\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C6H6ClN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2\\n\",\n        \"output\": \" -1.37\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methyl t-butyl ether \\n\",\n        \"output\": \" [C][O][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 5-Ethyl-5-phenylbarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Benzo(a)pyrene\\n\",\n        \"output\": \" c1ccc2c(c1)cc3ccc4cccc5ccc2c3c45\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Ethylene\\n\",\n        \"output\": \" [C][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl\\n\",\n        \"output\": \" Lindane\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" -2.658\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCCCCCCCCCCC\\n\",\n        \"output\": \" Tetradecane\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2\\n\",\n        \"output\": \" -0.244\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Triamterene\\n\",\n        \"output\": \" InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][I][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" p-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][S][C][C][Branch1][C][Cl][=C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 1.3182567385564074e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][O][C][C]\\n\",\n        \"output\": \" 3-Methyl-3-hexanol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Azobenzene\\n\",\n        \"output\": \" InChI=1S/C12H10N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" N(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 0.0003133285724315589 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyclopentene \\n\",\n        \"output\": \" InChI=1S/C5H8/c1-2-4-5-3-1/h1-2H,3-5H2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2\\n\",\n        \"output\": \" Erythritol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3\\n\",\n        \"output\": \" 0.00027478941531023943 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Bromoheptane\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Bromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" o-Aminophenol\\n\",\n        \"output\": \" InChI=1S/C6H7NO/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Tetrachloroethylene\\n\",\n        \"output\": \" InChI=1S/C2Cl4/c3-1(4)2(5)6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Methylbutane\\n\",\n        \"output\": \" [C][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" o-Hydroxybenzamide\\n\",\n        \"output\": \" NC(=O)c1ccccc1O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethyl propionate\\n\",\n        \"output\": \" [C][C][O][C][=Branch1][C][=O][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,2-Dimethylpropanol\\n\",\n        \"output\": \" InChI=1S/C5H12O/c1-5(2,3)4-6/h6H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Fluometuron\\n\",\n        \"output\": \" InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" o-Chloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H12N2O/c1-11(2)9(12)10-8-6-4-3-5-7-8/h3-7H,1-2H3,(H,10,12)\\n\",\n        \"output\": \" Fenuron\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H12O/c1-3-5(6)4-2/h5-6H,3-4H2,1-2H3\\n\",\n        \"output\": \" 3-Pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Mecarbam\\n\",\n        \"output\": \" InChI=1S/C10H20NO5PS2/c1-5-14-10(13)11(4)9(12)8-19-17(18,15-6-2)16-7-3/h5-8H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Methylpropene\\n\",\n        \"output\": \" CC(=C)C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" trans-2-Pentene \\n\",\n        \"output\": \" CC/C=C/C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14/c1-8(2)10-7-5-4-6-9(10)3/h4-8H,1-3H3\\n\",\n        \"output\": \" 2-Isopropyltoluene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" p-Chloronitrobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 7.762471166286912e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Oxadiazon\\n\",\n        \"output\": \" [C][C][Branch1][C][C][O][C][=C][C][=Branch1][#Branch2][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][N][N][=C][Branch1][=Branch1][O][C][Ring1][Branch1][=O][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H12/c1-7-5-3-2-4-6-7/h5H,2-4,6H2,1H3\\n\",\n        \"output\": \" 0.0005370317963702527 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4ClI/c7-5-2-1-3-6(8)4-5/h1-4H\\n\",\n        \"output\": \" m-Chloroiodobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Clc1cccc(c1Cl)c2cccc(Cl)c2Cl\\n\",\n        \"output\": \" 2,2',3,3'-PCB\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][O][P][=Branch1][C][=O][Branch1][Ring1][O][C][O][C][Branch1][C][Br][C][Branch1][C][Cl][Branch1][C][Cl][Br]\\n\",\n        \"output\": \" 0.005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" diisooctyl phthalate\\n\",\n        \"output\": \" -6.6370000000000005\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][Branch1][C][Br][=C][Branch1][C][Br][C][=C][Ring1][Branch2][Br]\\n\",\n        \"output\": \" 1,2,4,5-Tetrabromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C14H14/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H,11-12H2\\n\",\n        \"output\": \" -4.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C2H6/c1-2/h1-2H3\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Pentobarbital\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Chlorimuron-ethyl (ph 7)\\n\",\n        \"output\": \" InChI=1S/C15H15ClN4O6S/c1-3-26-14(22)10-6-4-5-7-11(10)27(23,24)19-20(9-21)15-17-12(16)8-13(18-15)25-2/h4-9,19H,3H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CC(C)(C)c1ccc(O)cc1\\n\",\n        \"output\": \" -2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Piperine\\n\",\n        \"output\": \" O=C(C=CC=Cc2ccc1OCOc1c2)N3CCCCC3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Ethyl-p-hydroxybenzoate \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H5N3O/c6-5(9)4-3-7-1-2-8-4/h1-3H,(H2,6,9)\\n\",\n        \"output\": \" Pyrazinamide\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Trifluralin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" 5-(3-Methyl-2-butenyl)-5-isoPrbarbital\\n\",\n        \"output\": \" -2.593\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Cc1cc(C)c(C)c(C)c1C\\n\",\n        \"output\": \" Pentamethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Tetrachloromethane\\n\",\n        \"output\": \" 0.004897788193684461 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Chloropropane\\n\",\n        \"output\": \" InChI=1S/C3H7Cl/c1-3(2)4/h3H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccc(O)c(C)c1\\n\",\n        \"output\": \" 0.06456542290346556 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C8H14ClNS2/c1-4-10(5-2)8(11)12-6-7(3)9/h3-6H2,1-2H3\\n\",\n        \"output\": \" 0.0004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" p-Xylene \\n\",\n        \"output\": \" InChI=1S/C8H10/c1-7-3-5-8(2)6-4-7/h3-6H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Oc1ccncc1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" ClC1=C(Cl)C(Cl)(C(=C1Cl)Cl)C2(Cl)C(=C(Cl)C(=C2Cl)Cl)Cl\\n\",\n        \"output\": \" -7.278\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H6N2O2/c1-7-3-2-4(8)6-5(7)9/h2-3H,1H3,(H,6,8,9)\\n\",\n        \"output\": \" 1-methyluracil\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" ClC(Cl)Cl\\n\",\n        \"output\": \" 0.06760829753919818 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC/C=C/C\\n\",\n        \"output\": \" trans-2-Pentene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Aminophenol\\n\",\n        \"output\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Nc1ccccc1Cl\\n\",\n        \"output\": \" 0.03019951720402016 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Butylate\\n\",\n        \"output\": \" 0.00020892961308540387 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" ClC1(C(=O)C2(Cl)C3(Cl)C14Cl)C5(Cl)C2(Cl)C3(Cl)C(Cl)(Cl)C45Cl\\n\",\n        \"output\": \" Kepone\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCc1cccc2ccccc12\\n\",\n        \"output\": \" 6.760829753919819e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,3-Dimethyl-1,3-Butadiene\\n\",\n        \"output\": \" 0.003981071705534973 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Pentachloroethane\\n\",\n        \"output\": \" -2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Tetrabromomethane\\n\",\n        \"output\": \" InChI=1S/CBr4/c2-1(3,4)5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][N][C]\\n\",\n        \"output\": \" Antipyrene\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H15ClNO4PS2/c1-3-16-19(20,17-4-2)21-8-14-10-6-5-9(13)7-11(10)18-12(14)15/h5-7H,3-4,8H2,1-2H3\\n\",\n        \"output\": \" Phosalone\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1cc(=O)n(c2ccccc2)n1C\\n\",\n        \"output\": \" 0.715\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][Branch2][Ring1][=Branch2][C][=C][Branch1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" -3.5610000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C19H26O12/c1-27-17(26)8-4-2-3-5-10(8)30-19-16(25)14(23)13(22)11(31-19)7-29-18-15(24)12(21)9(20)6-28-18/h2-5,9,11-16,18-25H,6-7H2,1H3\\n\",\n        \"output\": \" -0.742\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Flumetralin\\n\",\n        \"output\": \" [C][C][N][Branch1][=C][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][Cl][C][=C][Branch2][Ring1][=Branch1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][=N][C][=C][C][Branch1][#Branch1][C][=Branch1][C][=O][N][N][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" Isonazid\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Mefluidide\\n\",\n        \"output\": \" InChI=1S/C11H13F3N2O3S/c1-6-4-7(2)10(5-9(6)15-8(3)17)16-20(18,19)11(12,13)14/h4-5,16H,1-3H3,(H,15,17)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC12CC(O)C3C(CCC4=CC(=O)CCC34C)C2CCC1C(=O)CO\\n\",\n        \"output\": \" 0.0005754399373371566 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Ethyl acetate\\n\",\n        \"output\": \" -0.04\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-hydroxypteridine\\n\",\n        \"output\": \" InChI=1S/C6H4N4O/c11-6-9-3-4-5(10-6)8-2-1-7-4/h1-3H,(H,8,9,10,11)\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\\n\",\n        \"output\": \" -3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][Cl]\\n\",\n        \"output\": \" -0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1ccccc1(OC(=O)NC)\\n\",\n        \"output\": \" Metolcarb\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Fc1ccccc1\\n\",\n        \"output\": \" Fluorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" COP(=S)(OC)SCC(=O)N(C)C=O\\n\",\n        \"output\": \" 0.010115794542598982 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Picene\\n\",\n        \"output\": \" InChI=1S/C22H14/c1-3-7-17-15(5-1)9-11-21-19(17)13-14-20-18-8-4-2-6-16(18)10-12-22(20)21/h1-14H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" O=N(=O)c1cc(Cl)c(Cl)cc1\\n\",\n        \"output\": \" 3,4-Dichloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Metribuzin\\n\",\n        \"output\": \" -2.253\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 2-Ethylbutanal\\n\",\n        \"output\": \" CCC(CC)C=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" dibutyl sebacate\\n\",\n        \"output\": \" CCCCOC(=O)CCCCCCCCC(=O)OCCCC\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 1,3,5-Trichlorobenzene\\n\",\n        \"output\": \" 3.3113112148259076e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 3-Butanoyloxymethylphenytoin\\n\",\n        \"output\": \" InChI=1S/C20H20N2O4/c1-2-9-17(23)26-14-22-18(24)20(21-19(22)25,15-10-5-3-6-11-15)16-12-7-4-8-13-16/h3-8,10-13H,2,9,14H2,1H3,(H,21,25)\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Ethylbenzene\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCCCC(O)CC\\n\",\n        \"output\": \" 3-Heptanol \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C8H14O/c1-3-5-6-8(4-2)7-9/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 0.0034673685045253167 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" 3-Methyl-2-pentanol\\n\",\n        \"output\": \" 0.19498445997580455 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2-Methylpropane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=N][C][N][Branch1][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=N][=Ring1][#Branch2]\\n\",\n        \"output\": \" Caffeine\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" N-Methylaniline \\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.64\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H6ClN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2\\n\",\n        \"output\": \" m-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CCCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" -2.452\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)\\n\",\n        \"output\": \" 0.00047863009232263854 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c3ccc2nc1ccccc1cc2c3\\n\",\n        \"output\": \" Acridine\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C7H14O/c1-3-5-7(8)6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-3-5-4-2/h3H,1,4-5H2,2H3\\n\",\n        \"output\": \" -2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CC(=O)Nc1ccc(O)cc1\\n\",\n        \"output\": \" 0.0933254300796991 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H13N3O/c1-8-10(12)11(15)14(13(8)2)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3\\n\",\n        \"output\": \" ampyrone\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H12/c1-9-7-11-5-3-4-6-12(11)8-10(9)2/h3-8H,1-2H3\\n\",\n        \"output\": \" 2,3-Dimethylnaphthalene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCC(C)O\\n\",\n        \"output\": \" Butan-2-ol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H12O/c1-3-5-6(7)4-2/h3-5H2,1-2H3\\n\",\n        \"output\": \" 3-Hexanone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][=C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" DDE\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][=C][C][=Branch1][C][=O][O][C][Branch1][Ring1][C][#N][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][C][=C][Branch1][#Branch1][O][C][Branch1][C][F][F][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.33045441797809e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][Ring1][O][C][=N][Ring1][N]\\n\",\n        \"output\": \" Atratone\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.015848931924611134 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H8O2/c1-3-4(5)6-2/h3H2,1-2H3\\n\",\n        \"output\": \" Methyl propionate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Benzophenone\\n\",\n        \"output\": \" 0.0007585775750291836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C9H16ClN5/c1-4-11-8-12-7(10)13-9(14-8)15(5-2)6-3/h4-6H2,1-3H3,(H,11,12,13,14)\\n\",\n        \"output\": \" Trietazine\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4-Bromophenol\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1,1,1,2-Tetrachloroethane\\n\",\n        \"output\": \" ClCC(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 1,1,1-Trichloroethane\\n\",\n        \"output\": \" CC(Cl)(Cl)Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch1][#Branch1][C][=C][Branch1][C][Cl][Cl][C][Ring1][Branch2][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" Permethrin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][O][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][Branch1][C][O][C][#C]\\n\",\n        \"output\": \" -4.57\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H18O/c1-3-4-5-6-7-8(2)9/h8-9H,3-7H2,1-2H3\\n\",\n        \"output\": \" 2-Octanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" slip\\n\",\n        \"output\": \" slip does not have compound\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C4H10/c1-3-4-2/h3-4H2,1-2H3\\n\",\n        \"output\": \" -2.57\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" ClC(=C(Cl)Cl)Cl\\n\",\n        \"output\": \" Tetrachloroethylene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 2-Pentanol\\n\",\n        \"output\": \" [C][C][C][C][Branch1][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Brc1ccc2ccccc2c1\\n\",\n        \"output\": \" 2-Bromonapthalene\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Nc1ccc(cc1)c2ccc(N)cc2\\n\",\n        \"output\": \" p-benzidine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H19O2PS3/c1-4-9-11(12,10-5-2)14-8-7-13-6-3/h4-8H2,1-3H3\\n\",\n        \"output\": \" Disulfoton\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2-Isopropyltoluene\\n\",\n        \"output\": \" InChI=1S/C10H14/c1-8(2)10-7-5-4-6-9(10)3/h4-8H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Bromohexane\\n\",\n        \"output\": \" InChI=1S/C6H13Br/c1-2-3-4-5-6-7/h2-6H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Toluene \\n\",\n        \"output\": \" Cc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Bromoiodobenzene\\n\",\n        \"output\": \" Brc1ccc(I)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-4-5-7(2,3)6-8/h8H,4-6H2,1-3H3\\n\",\n        \"output\": \" 2,2-Dimethylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 6.165950018614822e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" Cyclooctane\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" trans-2-Heptene \\n\",\n        \"output\": \" 0.00015135612484362088 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Bibenzyl \\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCNc1ccccc1\\n\",\n        \"output\": \" N-Ethylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H16N2O3/c1-3-5-6-10(4-2)7(13)11-9(15)12-8(10)14/h3-6H2,1-2H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" Butethal\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1cccc(Br)c1\\n\",\n        \"output\": \" 0.0006165950018614823 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Niridazole\\n\",\n        \"output\": \" -3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" OC1CCCCCC1\\n\",\n        \"output\": \" -0.88\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2,2',3,4,5,5',6-PCB\\n\",\n        \"output\": \" Clc1ccc(Cl)c(c1)c2c(Cl)c(Cl)c(Cl)c(Cl)c2Cl\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C5H10/c1-4-5(2)3/h2,4H2,1,3H3\\n\",\n        \"output\": \" 2-Methyl-1-Butene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" citral\\n\",\n        \"output\": \" [C][C][Branch1][C][C][=C][C][C][C][Branch1][C][C][=C][C][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Chloroaniline\\n\",\n        \"output\": \" Nc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" -2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CCCCCCCC(C)O\\n\",\n        \"output\": \" 2-Nonanol\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CN(C(=O)NC(C)(C)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" Methyldymron\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 1-Hexene\\n\",\n        \"output\": \" CCCCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Propoxur\\n\",\n        \"output\": \" CNC(=O)Oc1ccccc1OC(C)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H\\n\",\n        \"output\": \" o-Chloronitrobenzene\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][Ring1][#Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" 2,6-Dimethylnaphthalene \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 5-Nonanone\\n\",\n        \"output\": \" CCCCC(=O)CCCC\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][I]\\n\",\n        \"output\": \" -1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H6N2O2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H,7H2\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Hydroxypyridine\\n\",\n        \"output\": \" [O][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C2HCl3/c3-1-2(4)5/h1H\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 5-Ethyl-5-isopropylbarbituric acid\\n\",\n        \"output\": \" InChI=1S/C9H14N2O3/c1-4-9(5(2)3)6(12)10-8(14)11-7(9)13/h5H,4H2,1-3H3,(H2,10,11,12,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCOC(=O)CC\\n\",\n        \"output\": \" -0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Oc1c(Cl)ccc(Cl)c1Cl\\n\",\n        \"output\": \" 0.0022908676527677724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,2-Dimethyl-1-butanol\\n\",\n        \"output\": \" InChI=1S/C6H14O/c1-4-6(2,3)5-7/h7H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 2-Ethyl-1-butanol\\n\",\n        \"output\": \" CCC(CC)CO\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" Methyl octanoate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cyanazine\\n\",\n        \"output\": \" CCNc1nc(Cl)nc(NC(C)(C)C#N)n1\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-Isopropyltoluene\\n\",\n        \"output\": \" InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4-8H,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Napthol\\n\",\n        \"output\": \" Oc1cccc2ccccc12\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][O][S][Branch1][C][C][=Branch1][C][=O][=O][C][=C][Ring1][O][C][Ring1][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" -3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" 1-Heptyne\\n\",\n        \"output\": \" 0.000977237220955811 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Acrylonitrile\\n\",\n        \"output\": \" [C][=C][C][#N]\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3.3113112148259076e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3\\n\",\n        \"output\": \" o-Methoxyphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Oxycarboxin\\n\",\n        \"output\": \" InChI=1S/C12H13NO4S/c1-9-11(18(15,16)8-7-17-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1,2,3,4-Tetrachlorobenzene\\n\",\n        \"output\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Triallate\\n\",\n        \"output\": \" InChI=1S/C10H16Cl3NOS/c1-6(2)14(7(3)4)10(15)16-5-8(11)9(12)13/h6-7H,5H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H19ClNO5P/c1-5-12(6-2)10(13)9(11)7-8-17-18(14,15-3)16-4/h7H,5-6,8H2,1-4H3\\n\",\n        \"output\": \" Dimecron\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.12302687708123815 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Chloramphenicol\\n\",\n        \"output\": \" InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" Norea\\n\",\n        \"output\": \" 0.0006745280276979215 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" Butabarbital\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Endrin\\n\",\n        \"output\": \" -6.18\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][Cl]\\n\",\n        \"output\": \" 2-Chloro-2-methylbutane\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Isazofos\\n\",\n        \"output\": \" [C][C][O][P][=Branch1][C][=S][Branch1][Ring2][O][C][C][O][C][N][=C][Branch1][C][Cl][N][Branch1][Ring2][N][=Ring1][=Branch1][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Chloroaniline\\n\",\n        \"output\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Pentanol\\n\",\n        \"output\": \" [C][C][C][C][C][O]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H\\n\",\n        \"output\": \" Phenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Hexamethylbenzene\\n\",\n        \"output\": \" InChI=1S/C12H18/c1-7-8(2)10(4)12(6)11(5)9(7)3/h1-6H3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H16O/c1-9(2)5-4-6-10(3)7-8-11/h5,7-8H,4,6H2,1-3H3\\n\",\n        \"output\": \" citral\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][C][C][S][C][Ring1][Ring1][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O]\\n\",\n        \"output\": \" Epitostanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" allicin\\n\",\n        \"output\": \" C=CCS(=O)SCC=C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C8H16/c1-2-4-6-8-7-5-3-1/h1-8H2\\n\",\n        \"output\": \" 7.079457843841373e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc3cc2nc1c(=O)[nH]c(=O)nc1n(CC(O)C(O)C(O)CO)c2cc3C\\n\",\n        \"output\": \" Riboflavin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Altretamine\\n\",\n        \"output\": \" InChI=1S/C9H18N6/c1-13(2)7-10-8(14(3)4)12-9(11-7)15(5)6/h1-6H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 1-Bromopropane\\n\",\n        \"output\": \" -1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Procymidone\\n\",\n        \"output\": \" -4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" 2-Ethylnaphthalene\\n\",\n        \"output\": \" 5.128613839913648e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Anethole\\n\",\n        \"output\": \" InChI=1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" OCCOc1ccccc1\\n\",\n        \"output\": \" 2-Phenoxyethanol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Isoproturon\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][Ring1][N]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H14O2/c1-6(2)4-5-9-7(3)8/h6H,4-5H2,1-3H3\\n\",\n        \"output\": \" Isopentyl acetate\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2-methoxypteridine\\n\",\n        \"output\": \" InChI=1S/C7H6N4O/c1-12-7-10-4-5-6(11-7)9-3-2-8-5/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" CCOP(=S)(OCC)SCn1c(=O)oc2cc(Cl)ccc12\\n\",\n        \"output\": \" -5.233\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its oil solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CC1(C)C(C(=O)OC(C#N)c2cccc(Oc3ccccc3)c2)C1(C)C\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Etofenprox\\n\",\n        \"output\": \" [C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C4H10O/c1-4(2)3-5/h4-5H,3H2,1-2H3\\n\",\n        \"output\": \" 2-Methylpropan-1-ol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1ccccc1n2ncc(N)c(Br)c2(=O)\\n\",\n        \"output\": \" brompyrazone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1cc(C)cc(O)c1\\n\",\n        \"output\": \" 3,5-Dimethylphenol\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)C\\n\",\n        \"output\": \" -2.148\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Amitrole\\n\",\n        \"output\": \" Nc1nc[nH]n1\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature? ->\",\n        \"input\": \" Epiandrosterone\\n\",\n        \"output\": \" -4.16\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H8S/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" -2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][O][C][C][Ring1][#Branch1][C][C][C][C][Ring1][O][C][C][C][Branch1][C][C][C][Ring1][#Branch1][C][C][C][Ring1][=Branch1][=O]\\n\",\n        \"output\": \" Androsterone\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=N(=O)c1c(Cl)c(Cl)ccc1\\n\",\n        \"output\": \" 0.0003311311214825911 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Chlorobenzene\\n\",\n        \"output\": \" Clc1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 4-Methylbiphenyl\\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Bromoethane\\n\",\n        \"output\": \" CCBr\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SMILES in room temperature. ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)N\\n\",\n        \"output\": \" 0.018197008586099836 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC(C)C1CCC(C)CC1=O\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][C][C][C][C][Branch1][Branch2][C][O][C][Ring1][=Branch1][Ring1][Ring1][C][Ring1][Branch2][C][Ring1][=C][Branch1][C][Cl][C][Ring1][=N][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Dieldrin\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Iodomethane\\n\",\n        \"output\": \" [C][I]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CCCC(C)C\\n\",\n        \"output\": \" 0.00018197008586099826 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" 4-methylpteridine\\n\",\n        \"output\": \" Cc1ncnc2nccnc12\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2\\n\",\n        \"output\": \" L-arabinose\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][=C][C][Branch1][N][C][Ring1][O][=C][C][Ring1][#C][=C][Ring2][Ring1][Ring1][=C][Ring1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.235936569296281e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H\\n\",\n        \"output\": \" 4.466835921509635e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" p-Chloronitrobenzene\\n\",\n        \"output\": \" 0.001202264434617413 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Nitromethane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][O][N][Branch1][#C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring1][=C][=O]\\n\",\n        \"output\": \" 0.0015135612484362087 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" kebuzone\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=C][Branch1][Ring1][C][C][C][=O]\\n\",\n        \"output\": \" 2-Ethyl-2-hexanal\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Clomazone\\n\",\n        \"output\": \" InChI=1S/C12H14ClNO2/c1-12(2)8-16-14(11(12)15)7-9-5-3-4-6-10(9)13/h3-6H,7-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CC(C)c1ccccc1\\n\",\n        \"output\": \" Isopropylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C14H11ClN2O4S/c15-11-6-5-8(7-12(11)22(16,20)21)14(19)10-4-2-1-3-9(10)13(18)17-14/h1-7,19H,(H,17,18)(H2,16,20,21)\\n\",\n        \"output\": \" -3.451\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H12N2O3/c1-3-5-9(4-2)6(12)10-8(14)11-7(9)13/h3H,1,4-5H2,2H3,(H2,10,11,12,13,14)\\n\",\n        \"output\": \" 5-Allyl-5-ethylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Flutriafol\\n\",\n        \"output\": \" [O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][F]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C10H10O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-6H,1-2H3\\n\",\n        \"output\": \" Dimethyl phthalate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][S][C][=C][C][=C][Branch1][C][Cl][N][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.019230917289101587 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Ethyl acetate\\n\",\n        \"output\": \" CCOC(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C17H20N2O/c1-17(2,14-10-6-4-7-11-14)18-16(20)19(3)15-12-8-5-9-13-15/h4-13H,1-3H3,(H,18,20)\\n\",\n        \"output\": \" 0.00044668359215096305 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Methylparaben\\n\",\n        \"output\": \" InChI=1S/C8H8O3/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5,9H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1ccccc1Br\\n\",\n        \"output\": \" -2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is solubility expressed as a logarithm in mol/L of given SMILES? ->\",\n        \"input\": \" COCOC\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H18/c1-7(2)6-8(3,4)5/h7H,6H2,1-5H3\\n\",\n        \"output\": \" 2,2,4-Trimethylpentane\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Flucytosine\\n\",\n        \"output\": \" 0.10665961212302578 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" [C][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.933254300796991 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 4-Ethyltoluene\\n\",\n        \"output\": \" [C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" c1c(OC)c(OC)C2C(=O)OCC2c1\\n\",\n        \"output\": \" meconin\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-methylpteridine\\n\",\n        \"output\": \" InChI=1S/C7H6N4/c1-5-6-7(11-4-10-5)9-3-2-8-6/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C7H7Cl/c1-6-2-4-7(8)5-3-6/h2-5H,1H3\\n\",\n        \"output\": \" -3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-2-4-6-5-3-1/h1-5H2\\n\",\n        \"output\": \" Tetrahydropyran \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H17O2PS3/c1-4-8-10(11,9-5-2)13-7-12-6-3/h4-7H2,1-3H3\\n\",\n        \"output\": \" Phorate\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" O=N(=O)c1ccccc1\\n\",\n        \"output\": \" -1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" C=C\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Oc1ccc(cc1)c2ccccc2\\n\",\n        \"output\": \" -3.48\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" giraffe\\n\",\n        \"output\": \" giraffe does not have SMILES\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Dibenzofurane\\n\",\n        \"output\": \" 2.5118864315095822e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][N][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Clonazepam\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Monotropitoside\\n\",\n        \"output\": \" InChI=1S/C19H26O12/c1-27-17(26)8-4-2-3-5-10(8)30-19-16(25)14(23)13(22)11(31-19)7-29-18-15(24)12(21)9(20)6-28-18/h2-5,9,11-16,18-25H,6-7H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Cyclopentane \\n\",\n        \"output\": \" 0.0022908676527677724 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Permethrin\\n\",\n        \"output\": \" -6.291\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Dexamethasone\\n\",\n        \"output\": \" InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H16Cl3NOS/c1-6(2)14(7(3)4)10(15)16-5-8(11)9(12)13/h6-7H,5H2,1-4H3\\n\",\n        \"output\": \" Triallate\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1-Tetradecanol\\n\",\n        \"output\": \" InChI=1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CCCCCCCC\\n\",\n        \"output\": \" 5.754399373371567e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Isobutyl acetate\\n\",\n        \"output\": \" InChI=1S/C6H12O2/c1-5(2)4-8-6(3)7/h5H,4H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C20H30O4/c1-3-5-7-11-15-23-19(21)17-13-9-10-14-18(17)20(22)24-16-12-8-6-4-2/h9-10,13-14H,3-8,11-12,15-16H2,1-2H3\\n\",\n        \"output\": \" -6.144\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Methyl acetate\\n\",\n        \"output\": \" [C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Chloropropane\\n\",\n        \"output\": \" [C][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" cis-2-Pentene\\n\",\n        \"output\": \" [C][C][/C][=C][\\\\C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=O]\\n\",\n        \"output\": \" Isopropyl formate\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" methyl laurate\\n\",\n        \"output\": \" [C][C][C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Isopentyl acetate\\n\",\n        \"output\": \" InChI=1S/C7H14O2/c1-6(2)4-5-9-7(3)8/h6H,4-5H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Branch1][C][C][C][Branch1][C][C][=C][Ring1][#Branch2][C]\\n\",\n        \"output\": \" Hexamethylbenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" Nitroethane\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H18Cl2N2O3/c1-8(2)21-12-7-11(9(16)6-10(12)17)19-14(20)22-13(18-19)15(3,4)5/h6-8H,1-5H3\\n\",\n        \"output\": \" Oxadiazon\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Linuron\\n\",\n        \"output\": \" -3.592\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dipropyl ether\\n\",\n        \"output\": \" CCCOCCC\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in room temperature. ->\",\n        \"input\": \" OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O\\n\",\n        \"output\": \" 2.280342072000418 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][S][C][S][=Branch1][C][=O][C][C][Branch1][Ring1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][NH1][C][=Branch1][C][=O][NH1][C][Ring1][Branch2][=O]\\n\",\n        \"output\": \" -1.9809999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCc1ccc(CC)cc1\\n\",\n        \"output\": \" 1,4-Diethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Nc1ccccc1\\n\",\n        \"output\": \" Aniline \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCC=C\\n\",\n        \"output\": \" 1-Heptene\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in room temperature? ->\",\n        \"input\": \" 4-Heptanone\\n\",\n        \"output\": \" 0.05011872336272722 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" CCCCCCCC#C\\n\",\n        \"output\": \" 1-Nonyne \\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H15ClN2O2/c1-18(2)15(19)17-12-5-9-14(10-6-12)20-13-7-3-11(16)4-8-13/h3-10H,1-2H3,(H,17,19)\\n\",\n        \"output\": \" Chloroxuron\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Cc1c(F)c(F)c(COC(=O)C2C(C=C(Cl)C(F)(F)F)C2(C)C)c(F)c1F\\n\",\n        \"output\": \" 4.775292736576902e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Carbromal\\n\",\n        \"output\": \" InChI=1S/C7H13BrN2O2/c1-3-7(8,4-2)5(11)10-6(9)12/h3-4H2,1-2H3,(H3,9,10,11,12)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" Ethylbenzene\\n\",\n        \"output\": \" 0.0016982436524617442 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-5(7)6(2,3)4/h5,7H,1-4H3\\n\",\n        \"output\": \" 0.23988329190194904 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 5-Methylchrysene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][C][Branch1][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][Branch1][C][C][I]\\n\",\n        \"output\": \" 2-Iodopropane\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Benzo(k)fluoranthene\\n\",\n        \"output\": \" InChI=1S/C20H12/c1-2-6-15-12-19-17-10-4-8-13-7-3-9-16(20(13)17)18(19)11-14(15)5-1/h1-12H\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" Diisopropyl ether \\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" N,N-Dimethylaniline\\n\",\n        \"output\": \" InChI=1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" Nimetazepam\\n\",\n        \"output\": \" 0.0001599558028614668 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Reposal\\n\",\n        \"output\": \" InChI=1S/C14H18N2O3/c1-2-14(11(17)15-13(19)16-12(14)18)10-6-4-8-3-5-9(10)7-8/h6,8-9H,2-5,7H2,1H3,(H2,15,16,17,18,19)\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 3-Methyl-2-butanol\\n\",\n        \"output\": \" 0.660693448007596 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Cycloheptene\\n\",\n        \"output\": \" C1CCC=CCC1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 0.019054607179632473 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Bromobenzene\\n\",\n        \"output\": \" [Br][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C]\\n\",\n        \"output\": \" -8.172\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Clc1ccccc1Cl\\n\",\n        \"output\": \" 1,2-Dichlorobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OC(c1ccc(Cl)cc1)(c2cncnc2)c3ccccc3Cl\\n\",\n        \"output\": \" Fenarimol\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 1-Napthol\\n\",\n        \"output\": \" InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given compound in 25 \\u00b0C? ->\",\n        \"input\": \" 2,3-Dimethylpentane\\n\",\n        \"output\": \" -4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" m-Chloroaniline\\n\",\n        \"output\": \" InChI=1S/C6H6ClN/c7-5-2-1-3-6(8)4-5/h1-4H,8H2\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H\\n\",\n        \"output\": \" Bromobenzene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" OCC(O)CO\\n\",\n        \"output\": \" Glycerol\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 3-Octanoyloxymethylphenytoin\\n\",\n        \"output\": \" O=C1N(COC(=O)CCCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [Br][C][Branch1][C][Br][Br]\\n\",\n        \"output\": \" -1.91\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Fenthion\\n\",\n        \"output\": \" COP(=S)(OC)Oc1ccc(SC)c(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 1-Nitropropane\\n\",\n        \"output\": \" [C][C][C][N][=Branch1][C][=O][=O]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" thioanisole\\n\",\n        \"output\": \" [C][=C][C][=C][C][=C][Ring1][=Branch1][S][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -2.843\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Phthalonitrile\\n\",\n        \"output\": \" [N][#C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][#N]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" o-Toluidine\\n\",\n        \"output\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C13H12N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H,(H2,14,15,16)\\n\",\n        \"output\": \" Carbanilide\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][C]\\n\",\n        \"output\": \" 0.08709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][=N]\\n\",\n        \"output\": \" -3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" c1ccc2c3c(ccc2c1)c4cccc5cccc3c45\\n\",\n        \"output\": \" 1e-08 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H30N2O5S/c1-7-25-17(23)11-12-22(14(2)3)28-21(6)19(24)26-16-10-8-9-15-13-20(4,5)27-18(15)16/h8-10,14H,7,11-13H2,1-6H3\\n\",\n        \"output\": \" Benfuracarb\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H14O2/c1-3-7-5-6-8-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" 1,2-Diethoxyethane \\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [Cl][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" Tetrachloromethane\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][O]\\n\",\n        \"output\": \" -2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Cl]\\n\",\n        \"output\": \" 0.01096478196143185 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Trifluralin\\n\",\n        \"output\": \" CCCN(CCC)c1c(cc(cc1N(=O)=O)C(F)(F)F)N(=O)=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1,4-Diethylbenzene \\n\",\n        \"output\": \" [C][C][C][=C][C][=C][Branch1][Ring1][C][C][C][=C][Ring1][Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Dyphylline\\n\",\n        \"output\": \" Cn2c(=O)n(C)c1ncn(CC(O)CO)c1c2=O\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2]\\n\",\n        \"output\": \" Indan\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,2,5-Trimethylhexane\\n\",\n        \"output\": \" InChI=1S/C9H20/c1-8(2)6-7-9(3,4)5/h8H,6-7H2,1-5H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [Cl][C][=Branch1][C][=C][Cl]\\n\",\n        \"output\": \" -1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-1-5(8)3-6(9)2-4/h1-3,9H\\n\",\n        \"output\": \" 0.04570881896148749 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 4-Chlorophenol \\n\",\n        \"output\": \" InChI=1S/C6H5ClO/c7-5-1-3-6(8)4-2-5/h1-4,8H\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H10Cl2O2/c14-10-1-3-12(16)8(6-10)5-9-7-11(15)2-4-13(9)17/h1-4,6-7,16-17H,5H2\\n\",\n        \"output\": \" Dichlorophen\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Bromooctane\\n\",\n        \"output\": \" CCCCCCCCBr\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Cyhalothrin\\n\",\n        \"output\": \" InChI=1S/C23H19ClF3NO3/c1-22(2)17(12-19(24)23(25,26)27)20(22)21(29)31-18(13-28)14-7-6-10-16(11-14)30-15-8-4-3-5-9-15/h3-12,17-18,20H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" COC1=CC(=O)CC(C)C13Oc2c(Cl)c(OC)cc(OC)c2C3=O\\n\",\n        \"output\": \" -3.2460000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Prometryn\\n\",\n        \"output\": \" [C][S][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][=C]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" t-Pentylbenzene\\n\",\n        \"output\": \" [C][C][Branch1][C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Aminocarb\\n\",\n        \"output\": \" CNC(=O)Oc1ccc(N(C)C)c(C)c1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][=C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.005584701947368306 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Nc1cccc(Cl)c1\\n\",\n        \"output\": \" m-Chloroaniline\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][O][Ring1][P]\\n\",\n        \"output\": \" Oxycarboxin\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in room temperature? ->\",\n        \"input\": \" Nc1ccc(Cl)cc1\\n\",\n        \"output\": \" 0.02187761623949553 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][O][C]\\n\",\n        \"output\": \" -0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" Nc1nc[nH]n1\\n\",\n        \"output\": \" Amitrole\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" Acetanilide\\n\",\n        \"output\": \" -1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H32O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h10,16-18,20,26,28H,4-9,11-12H2,1-3H3\\n\",\n        \"output\": \" Hydrocortisone 21-acetate\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3\\n\",\n        \"output\": \" Anisole\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Perylene\\n\",\n        \"output\": \" 1.5703628043335515e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][#C]\\n\",\n        \"output\": \" Propyne\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][#Branch1][N][C][Branch1][C][C][C][=N][Ring1][O]\\n\",\n        \"output\": \" -3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" COc1ccc(cc1)C(c2ccc(OC)cc2)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" Methoxychlor\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,4,5-Trichlorophenol \\n\",\n        \"output\": \" InChI=1S/C6H3Cl3O/c7-3-1-5(9)6(10)2-4(3)8/h1-2,10H\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC34CCC1C(CCC2CC(O)CCC12C)C3CCC4=O\\n\",\n        \"output\": \" -4.16\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 1,2-Dichloropropane\\n\",\n        \"output\": \" InChI=1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Oc1ccc(Br)cc1\\n\",\n        \"output\": \" -1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1cc(no1)C(=O)NNCc2ccccc2\\n\",\n        \"output\": \" -2.461\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 2-Methylpropene\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H22O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-10H2,1H3\\n\",\n        \"output\": \" 1-Decanol\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" Butamben\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C4H8/c1-4(2)3/h1H2,2-3H3\\n\",\n        \"output\": \" -2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its aqueous solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" difluron\\n\",\n        \"output\": \" -6.02\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Phenetole\\n\",\n        \"output\": \" 0.004677351412871981 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 5,5-Dimethylbarbituric acid\\n\",\n        \"output\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" Cn2c(=O)n(C)c1ncn(CC(O)CO)c1c2=O\\n\",\n        \"output\": \" 0.6760829753919817 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1N(COC(=O)CCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 1.30016957803329e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [O][=C][N][Branch1][N][C][O][C][=Branch1][C][=O][C][C][C][C][C][C][=Branch1][C][=O][C][Branch1][Ring2][N][Ring1][#C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.30016957803329e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" Cc1ccc2c(ccc3ccccc32)c1\\n\",\n        \"output\": \" 2-Methylphenanthrene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Buthidazole\\n\",\n        \"output\": \" [C][N][C][C][Branch1][C][O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][Branch1][C][C][Branch1][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC34CCC1C(CCC2=CC(=O)CCC12O)C3CCC4(O)C#C\\n\",\n        \"output\": \" -4.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" CCCC(C)(C)C\\n\",\n        \"output\": \" 4.3651583224016566e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H12ClN3O3S/c1-2-9-13-7-4-6(11)8(18(12,16)17)3-5(7)10(15)14-9/h3-4,9,13H,2H2,1H3,(H,14,15)(H2,12,16,17)\\n\",\n        \"output\": \" -3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cn1ccc(=O)[nH]c1=O\\n\",\n        \"output\": \" -0.807\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" 1,2,4-Trimethylbenzene\\n\",\n        \"output\": \" -3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Fluoranthene\\n\",\n        \"output\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given compound in room temperature? ->\",\n        \"input\": \" 2-Chlorophenol\\n\",\n        \"output\": \" 0.08709635899560805 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C5H8/c1-3-5-4-2/h3-4H,1-2,5H2\\n\",\n        \"output\": \" -2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Clc1ccc(Br)cc1\\n\",\n        \"output\": \" -3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C11H23NOS/c1-6-14-11(13)12(7-9(2)3)8-10(4)5/h9-10H,6-8H2,1-5H3\\n\",\n        \"output\": \" Butylate\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" ampyrone\\n\",\n        \"output\": \" Cc2c(N)c(=O)n(c1ccccc1)n2C\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C8H7NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-6H,(H,9,10,11)\\n\",\n        \"output\": \" phthalamide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Methylcyclopentane\\n\",\n        \"output\": \" CC1CCCC1\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C10H20NO5PS2/c1-5-14-10(13)11(4)9(12)8-19-17(18,15-6-2)16-7-3/h5-8H2,1-4H3\\n\",\n        \"output\": \" 0.0030338911841942687 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given InChI in room temperature? ->\",\n        \"input\": \" InChI=1S/C6H14S/c1-3-5-7-6-4-2/h3-6H2,1-2H3\\n\",\n        \"output\": \" 0.0026302679918953813 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" 1,2-Diethoxyethane \\n\",\n        \"output\": \" -0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H8Cl3NO3/c14-8(15)5-9(18)17-11-10(16)12(19)6-3-1-2-4-7(6)13(11)20/h1-4,8H,5H2,(H,17,18)\\n\",\n        \"output\": \" Quinonamid\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in 25 \\u00b0C. ->\",\n        \"input\": \" Cypermethrin\\n\",\n        \"output\": \" 9.616122783836619e-09 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C17H12/c1-2-6-13-11-17-15(9-12(13)5-1)10-14-7-3-4-8-16(14)17/h1-9,11H,10H2\\n\",\n        \"output\": \" Benzo(b)fluorene\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" 1-Iodonapthalene\\n\",\n        \"output\": \" [I][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Epitostanol\\n\",\n        \"output\": \" InChI=1S/C19H30OS/c1-18-8-7-14-12(13(18)5-6-17(18)20)4-3-11-9-15-16(21-15)10-19(11,14)2/h11-17,20H,3-10H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" Cc1ccc(N)cc1\\n\",\n        \"output\": \" 0.06165950018614822 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" O=C1N(COC(=O)CC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 1.238796586530369e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H20NO4PS/c1-6-11-16(17,13-5)15-9(4)7-10(12)14-8(2)3/h7-8H,6H2,1-5H3,(H,11,17)\\n\",\n        \"output\": \" Propetamphos\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2\\n\",\n        \"output\": \" Decalin\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" gentisin\\n\",\n        \"output\": \" InChI=1S/C14H14O5/c1-18-8-5-10(16)13-12(6-8)19-11-3-2-7(15)4-9(11)14(13)17/h2-6,9,11-13,15-16H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" m-Methylaniline\\n\",\n        \"output\": \" InChI=1S/C7H9N/c1-6-3-2-4-7(8)5-6/h2-5H,8H2,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given InChI in 25 \\u00b0C? ->\",\n        \"input\": \" InChI=1S/C19H21ClN2O/c20-16-12-10-15(11-13-16)14-22(18-8-4-5-9-18)19(23)21-17-6-2-1-3-7-17/h1-3,6-7,10-13,18H,4-5,8-9,14H2,(H,21,23)\\n\",\n        \"output\": \" -5.915\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SMILES in room temperature? ->\",\n        \"input\": \" CSCS(=O)CC(CO)NC(=O)C=Cc1c(C)[nH]c(=O)[nH]c1=O\\n\",\n        \"output\": \" 0.010447202192208004 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3\\n\",\n        \"output\": \" 1-Pentadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H16/c1-3-5-7-6-4-2/h3-7H2,1-2H3\\n\",\n        \"output\": \" 2.951209226666384e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility expressed as a logarithm in mol/L of given SELFIES in 25 \\u00b0C? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Branch1][C][C][C][=C][C][Ring1][#Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" -4.89\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Perfluidone\\n\",\n        \"output\": \" 0.00015848931924611142 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is aqueous solubility of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][Ring1][O]\\n\",\n        \"output\": \" 5.4954087385762485e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given compound in room temperature. ->\",\n        \"input\": \" 2-Methyltetrahydrofurane\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H16O/c1-2-3-4-5-6-7-8/h8H,2-7H2,1H3\\n\",\n        \"output\": \" 1-Heptanol\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [Br][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.028840315031266057 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CCOP(=S)(OCC)SC(CCl)N2C(=O)c1ccccc1C2=O\\n\",\n        \"output\": \" 4.5708818961487516e-07 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" N,N-Dimethylacetamide\\n\",\n        \"output\": \" CN(C)C(=O)C\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" c1cc2cccc3c4cccc5cccc(c(c1)c23)c54\\n\",\n        \"output\": \" Perylene\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" Perylene\\n\",\n        \"output\": \" c1cc2cccc3c4cccc5cccc(c(c1)c23)c54\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" InChI=1S/C7H7ClO/c1-9-7-5-3-2-4-6(7)8/h2-5H,1H3\\n\",\n        \"output\": \" -2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SMILES in room temperature? ->\",\n        \"input\": \" CC(C)CC(C)O\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" InChI=1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2\\n\",\n        \"output\": \" -3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given InChI in room temperature. ->\",\n        \"input\": \" InChI=1S/C18H12/c1-3-7-15-13(5-1)9-11-18-16-8-4-2-6-14(16)10-12-17(15)18/h1-12H\\n\",\n        \"output\": \" -8.057\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its aqueous solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" 2-Bromopropane\\n\",\n        \"output\": \" [C][C][Branch1][C][C][Br]\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" Glafenine\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" InChI=1S/C5H10O/c1-4(2)5(3)6/h4H,1-3H3\\n\",\n        \"output\": \" 0.7585775750291838 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Fenuron\\n\",\n        \"output\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Siduron\\n\",\n        \"output\": \" CC1CCCCC1NC(=O)Nc2ccccc2\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][=C][C][C][/C][Branch1][C][C][=C][\\\\C][O]\\n\",\n        \"output\": \" Nerol\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C6H14O/c1-6(2)4-3-5-7/h6-7H,3-5H2,1-2H3\\n\",\n        \"output\": \" 4-Methylpentanol\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Methyl propionate\\n\",\n        \"output\": \" [C][C][C][=Branch1][C][=O][O][C]\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][Branch1][Ring1][C][C][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1,4-Diethylbenzene \\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Isopentyl acetate\\n\",\n        \"output\": \" [C][C][Branch1][C][C][C][C][O][C][=Branch1][C][=O][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Dibutyl ether \\n\",\n        \"output\": \" InChI=1S/C8H18O/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility in room temperature. ->\",\n        \"input\": \" Chlorothalonil\\n\",\n        \"output\": \" 2.2908676527677747e-06 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Primidone\\n\",\n        \"output\": \" InChI=1S/C12H14N2O2/c1-2-12(9-6-4-3-5-7-9)10(15)13-8-14-11(12)16/h3-7H,2,8H2,1H3,(H,13,15)(H,14,16)\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H9N/c1-6-3-2-4-7(8)5-6/h2-5H,8H2,1H3\\n\",\n        \"output\": \" m-Methylaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" O=C1NC(=O)NC(=O)C1(C(C)C)CC=C(C)C\\n\",\n        \"output\": \" 5-(3-Methyl-2-butenyl)-5-isoPrbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" C(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" -4.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" Acetamide\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SMILES. ->\",\n        \"input\": \" p-Chloroacetanilide\\n\",\n        \"output\": \" CC(=O)Nc1ccc(Cl)cc1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CNC(=O)Oc1ccccc1C2OCCO2\\n\",\n        \"output\": \" Dioxacarb\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its water solubility expressed as a logarithm in mol/L in room temperature. ->\",\n        \"input\": \" Hexachloroethane\\n\",\n        \"output\": \" -3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility of given SMILES in 25 \\u00b0C? ->\",\n        \"input\": \" CC1(C)CON(Cc2ccccc2Cl)C1=O\\n\",\n        \"output\": \" 0.004591980128368685 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its water solubility expressed as a logarithm in mol/L in 25 \\u00b0C. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -4.38\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][Branch2][Branch1][Ring1][C][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 5-Ethyl-5-(3-methylbutyl)barbital\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H\\n\",\n        \"output\": \" d-inositol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in 25 \\u00b0C. ->\",\n        \"input\": \" c1ccc(Cl)cc1C(c2ccc(Cl)cc2)(O)C(=O)OC(C)C\\n\",\n        \"output\": \" 2.951209226666384e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][N][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 2,6-Dinitrotoluene\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H16Cl2O3/c1-11(2)22-16(20)17(21,12-6-8-14(18)9-7-12)13-4-3-5-15(19)10-13/h3-11,21H,1-2H3\\n\",\n        \"output\": \" chloropropylate\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its water solubility in room temperature. ->\",\n        \"input\": \" CCc1ccccc1CC\\n\",\n        \"output\": \" 0.0005248074602497728 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" Rovral\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][S][C][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Fenothiocarb\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H8/c1-3-5-4-2/h1H,4-5H2,2H3\\n\",\n        \"output\": \" 1-Pentyne\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)\\n\",\n        \"output\": \" Lorazepam\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][#C]\\n\",\n        \"output\": \" -3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" p-Xylene \\n\",\n        \"output\": \" [C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" 1-Dodecanol\\n\",\n        \"output\": \" CCCCCCCCCCCCO\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Furfural\\n\",\n        \"output\": \" O=Cc1ccco1\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given SMILES. ->\",\n        \"input\": \" Oc1ccc(Cl)cc1Cc2cc(Cl)ccc2O\\n\",\n        \"output\": \" Dichlorophen\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Iodofenphos\\n\",\n        \"output\": \" COP(=S)(OC)Oc1cc(Cl)c(I)cc1Cl\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" Isopropylbenzene \\n\",\n        \"output\": \" InChI=1S/C9H12/c1-8(2)9-6-4-3-5-7-9/h3-8H,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][C][O]\\n\",\n        \"output\": \" 1-Octadecanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)C(C)O\\n\",\n        \"output\": \" 3-Methyl-2-butanol\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" o-Nitroaniline\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Pentobarbital\\n\",\n        \"output\": \" O=C1NC(=O)NC(=O)C1(CC)C(C)CCC\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H8O3/c1-11-8(10)6-2-4-7(9)5-3-6/h2-5,9H,1H3\\n\",\n        \"output\": \" Methylparaben\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC=C\\n\",\n        \"output\": \" Propylene\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" 9-Methylanthracene\\n\",\n        \"output\": \" Cc1c2ccccc2cc3ccccc13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCCCCCCCO\\n\",\n        \"output\": \" 0.004073802778041126 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Azodrin\\n\",\n        \"output\": \" InChI=1S/C7H14NO5P/c1-6(5-7(9)8-2)13-14(10,11-3)12-4/h5H,1-4H3,(H,8,9)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" O=C1N(COC(=O)CCCCCC)C(=O)C(N1)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3-Heptanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Phoxim\\n\",\n        \"output\": \" CCOP(=S)(OCC)ON=C(C#N)c1ccccc1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given SELFIES in room temperature. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C][Branch2][Ring1][=C][C][C][C][C][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][C][Ring1][O][C][C][C][Ring2][Ring1][C][Ring1][#C][C][C][#C]\\n\",\n        \"output\": \" 1.584893192461114e-05 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility expressed as a logarithm in mol/L of given SMILES in room temperature. ->\",\n        \"input\": \" CCCCCCCCCCCCCC\\n\",\n        \"output\": \" -7.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its compound. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][C][=N][C][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 7-methoxypteridine\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" Cyclobutyl-5-spirobarbituric acid\\n\",\n        \"output\": \" InChI=1S/C7H8N2O3/c10-4-7(2-1-3-7)5(11)9-6(12)8-4/h1-3H2,(H2,8,9,10,11,12)\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" 1-Chlorobutane\\n\",\n        \"output\": \" [C][C][C][C][Cl]\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Menthone\\n\",\n        \"output\": \" CC(C)C1CCC(C)CC1=O\\n\"\n    },\n    {\n        \"instruction\": \"What will be SELFIES of given compound? ->\",\n        \"input\": \" Disulfiram\\n\",\n        \"output\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=S][S][S][C][=Branch1][C][=S][N][Branch1][Ring1][C][C][C][C]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its potential SELFIES. ->\",\n        \"input\": \" Fluridone\\n\",\n        \"output\": \" [C][N][C][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][Ring2][=C][Ring1][=N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its compound. ->\",\n        \"input\": \" InChI=1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)\\n\",\n        \"output\": \" Carboxin\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H\\n\",\n        \"output\": \" 2,4-Dichlorophenol \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 5-Ethyl-5-(3-methylbutyl)barbital\\n\",\n        \"output\": \" InChI=1S/C11H18N2O3/c1-4-11(6-5-7(2)3)8(14)12-10(16)13-9(11)15/h7H,4-6H2,1-3H3,(H2,12,13,14,15,16)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CCOC(=O)c1ccccc1\\n\",\n        \"output\": \" Ethyl benzoate \\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" 2,2-Dimethylpentane\\n\",\n        \"output\": \" InChI=1S/C7H16/c1-5-6-7(2,3)4/h5-6H2,1-4H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SELFIES in 25 \\u00b0C. ->\",\n        \"input\": \" [C][C][Branch2][Ring1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][#C]\\n\",\n        \"output\": \" 0.0024154608344449406 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" Pyridine\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SELFIES of given compound. ->\",\n        \"input\": \" Anethole\\n\",\n        \"output\": \" [C][O][C][=C][C][=C][Branch1][Ring2][C][=C][C][C][=C][Ring1][=Branch2]\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" Permethrin\\n\",\n        \"output\": \" InChI=1S/C21H20Cl2O3/c1-21(2)17(12-18(22)23)19(21)20(24)25-13-14-7-6-10-16(11-14)26-15-8-4-3-5-9-15/h3-12,17,19H,13H2,1-2H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" CC3C2CCC1(C)C=CC(=O)C(=C1C2OC3=O)C\\n\",\n        \"output\": \" 0.0008128305161640995 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H9Cl/c13-12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H\\n\",\n        \"output\": \" 3-Chlorobiphenyl\\n\"\n    },\n    {\n        \"instruction\": \"What will be SMILES of given compound? ->\",\n        \"input\": \" Cyclohexanol \\n\",\n        \"output\": \" OC1CCCCC1\\n\"\n    },\n    {\n        \"instruction\": \"Write water solubility of given compound in room temperature. ->\",\n        \"input\": \" Oxycarboxin\\n\",\n        \"output\": \" 0.0052360043658575 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"Write solubility expressed as a logarithm in mol/L of given SMILES in 25 \\u00b0C. ->\",\n        \"input\": \" Cc1c(F)c(F)c(COC(=O)C2C(C=C(Cl)C(F)(F)F)C2(C)C)c(F)c1F\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its aqueous solubility in room temperature. ->\",\n        \"input\": \" CCC(C)C\\n\",\n        \"output\": \" 0.0006606934480075957 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SMILES? ->\",\n        \"input\": \" CC2(C)C1CCC(C)(C1)C2=O\\n\",\n        \"output\": \" D-fenchone\\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" 2,6-Dinitrotoluene\\n\",\n        \"output\": \" InChI=1S/C7H6N2O4/c1-5-6(8(10)11)3-2-4-7(5)9(12)13/h2-4H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its compound. ->\",\n        \"input\": \" CC(C)CC(C)O\\n\",\n        \"output\": \" 4-Methyl-2-pentanol\\n\"\n    },\n    {\n        \"instruction\": \"What is water solubility expressed as a logarithm in mol/L of given SELFIES in room temperature? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" -1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H16N2O4/c1-13(21)24-12-20-16(22)18(19-17(20)23,14-8-4-2-5-9-14)15-10-6-3-7-11-15/h2-11H,12H2,1H3,(H,19,23)\\n\",\n        \"output\": \" 3-Ethanoyloxymethylphenytoin\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch2][Ring1][O][O][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C]\\n\",\n        \"output\": \" Vinclozolin\\n\"\n    },\n    {\n        \"instruction\": \"Write InChI of given compound. ->\",\n        \"input\": \" p-Methoxybenzaldehyde\\n\",\n        \"output\": \" InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"What is compound of given SELFIES? ->\",\n        \"input\": \" [C][O][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" Methyl t-butyl ether \\n\"\n    },\n    {\n        \"instruction\": \"Given compound, write its InChI. ->\",\n        \"input\": \" o-Nitroanisole\\n\",\n        \"output\": \" InChI=1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3\\n\"\n    },\n    {\n        \"instruction\": \"Write aqueous solubility of given compound in room temperature. ->\",\n        \"input\": \" p-Chloroaniline\\n\",\n        \"output\": \" 0.02187761623949553 mol/L\\n\"\n    },\n    {\n        \"instruction\": \"What is InChI of given compound? ->\",\n        \"input\": \" 2,2-Dimethylpentanol\\n\",\n        \"output\": \" InChI=1S/C7H16O/c1-4-5-7(2,3)6-8/h8H,4-6H2,1-3H3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible SMILES of given compound. ->\",\n        \"input\": \" Chlorbufam\\n\",\n        \"output\": \" CC(OC(=O)Nc1cccc(Cl)c1)C#C\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17)\\n\",\n        \"output\": \" 5-Ethyl-5-phenylbarbital\\n\"\n    },\n    {\n        \"instruction\": \"Write compound of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3\\n\",\n        \"output\": \" 1,8-Cineole\\n\"\n    }\n]"
  },
  {
    "path": "dataset/ESOL/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 7,\n   \"id\": \"4d8c331b\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import random\\n\",\n    \"\\n\",\n    \"def random_generate_1(p, solu_num):\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    ran2 = random.randint(0,1)\\n\",\n    \"    ran3 = random.randint(0,1)\\n\",\n    \"    ran4 = random.randint(0,1)\\n\",\n    \"    if ran2 == 0:\\n\",\n    \"        liq = \\\"aqueous \\\"\\n\",\n    \"    else:\\n\",\n    \"        liq = \\\"water \\\"\\n\",\n    \"    ran3 = random.randint(0,1)\\n\",\n    \"    if ran3 == 0:\\n\",\n    \"        tem = \\\" in room temperature\\\"\\n\",\n    \"    else:\\n\",\n    \"        tem = \\\" in 25 °C\\\"\\n\",\n    \"    if ran4 == 0:\\n\",\n    \"        solubility = \\\"solubility\\\"\\n\",\n    \"        output = \\\" \\\"+str(pow(10, float(solu_num)))+\\\" mol/L\\\\n\\\"\\n\",\n    \"    else:\\n\",\n    \"        solubility = p[0]\\n\",\n    \"        output = \\\" \\\"+solu_num+\\\"\\\\n\\\"\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What is \\\"+ liq + solubility + \\\" of given \\\" + p[1] + tem + \\\"? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write \\\" + liq + solubility + \\\" of given \\\" + p[1] + tem + \\\". ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ liq + solubility + tem + \\\". ->\\\"\\n\",\n    \"    return question, output\\n\",\n    \"\\n\",\n    \"def random_generate_2(p):\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What is \\\"+ p[0]+\\\" of given \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write \\\"+ p[0]+ \\\" of given \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ p[0] + \\\". ->\\\"\\n\",\n    \"    return question\\n\",\n    \"\\n\",\n    \"def random_generate_3(p):\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What will be \\\"+ p[0]+\\\" of given \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write a possible \\\"+ p[0]+ \\\" of given \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given \\\" + p[1] + \\\", write its potential \\\"+ p[0] + \\\". ->\\\"\\n\",\n    \"    return question\\n\",\n    \"\\n\",\n    \"def random_generate_4(p):\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    ran2 = random.randint(0,1)\\n\",\n    \"    ran3 = random.randint(0,2)\\n\",\n    \"    ran4 = random.randint(0,1)\\n\",\n    \"    if ran2 == 0:\\n\",\n    \"        liq = \\\"\\\"\\n\",\n    \"    else:\\n\",\n    \"        liq = \\\"oil \\\"\\n\",\n    \"    if ran3 == 0:\\n\",\n    \"        tem = \\\" in room temperature\\\"\\n\",\n    \"    elif ran3 == 1:\\n\",\n    \"        tem = \\\" in 25 °C\\\"\\n\",\n    \"    elif ran3 == 2:\\n\",\n    \"        tem = \\\"\\\"\\n\",\n    \"    if ran4 == 0:\\n\",\n    \"        solubility = \\\"solubility\\\"\\n\",\n    \"    else:\\n\",\n    \"        solubility = p[0]\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What is \\\"+ liq + solubility + \\\" of given \\\" + p[1] + tem + \\\"? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write \\\" + liq + solubility + \\\" of given \\\" + p[1] + tem + \\\". ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ liq + solubility + tem + \\\". ->\\\"\\n\",\n    \"    return question\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 8,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"9270\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('ESOL.csv')\\n\",\n    \"slot = {\\\"compound\\\":\\\"Compound\\\", \\n\",\n    \"        \\\"solubility expressed as a logarithm in mol/L\\\":\\\"solubility_log in mol/L (solubility expressed as a logarithm in mol/L)\\\", \\n\",\n    \"        \\\"SMILES\\\":\\\"SMILES\\\", \\n\",\n    \"        \\\"SELFIES\\\":\\\"SELFIES\\\",\\n\",\n    \"        \\\"InChI\\\":\\\"InChI\\\"}\\n\",\n    \"pair1 = [(\\\"solubility expressed as a logarithm in mol/L\\\", \\\"compound\\\"),\\n\",\n    \"        (\\\"compound\\\", \\\"SMILES\\\"),\\n\",\n    \"        (\\\"compound\\\", \\\"SELFIES\\\"), \\n\",\n    \"        (\\\"compound\\\", \\\"InChI\\\"), \\n\",\n    \"        (\\\"InChI\\\", \\\"compound\\\"),\\n\",\n    \"        (\\\"solubility expressed as a logarithm in mol/L\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"solubility expressed as a logarithm in mol/L\\\", \\\"SELFIES\\\"),\\n\",\n    \"        (\\\"solubility expressed as a logarithm in mol/L\\\", \\\"InChI\\\")]\\n\",\n    \"pair2 = [(\\\"SMILES\\\", \\\"compound\\\"),\\n\",\n    \"         (\\\"SELFIES\\\", \\\"compound\\\")]\\n\",\n    \"data_list = []\\n\",\n    \"for df_slice in df.iterrows():\\n\",\n    \"    for p in pair1:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran1 = random.randint(0,2)\\n\",\n    \"        if p[0] == \\\"solubility expressed as a logarithm in mol/L\\\":\\n\",\n    \"            question, output = random_generate_1(p, str(df_slice[1][slot[p[0]]]))\\n\",\n    \"        else:\\n\",\n    \"            question = random_generate_2(p)\\n\",\n    \"            output = \\\" \\\"+str(df_slice[1][slot[p[0]]])+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] = \\\" \\\"+str(df_slice[1][slot[p[1]]])+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = output\\n\",\n    \"        data_list.append(tmp_dict)\\n\",\n    \"    for p in pair2:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        question = random_generate_3(p)\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] =  \\\" \\\"+str(df_slice[1][slot[p[1]]])+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(df_slice[1][slot[p[0]]])+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\\n\",\n    \"print(len(data_list))\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 9,\n   \"id\": \"6fd0e584\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"927\\n\",\n      \"18\\n\",\n      \"9342\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"# add unable to answer question\\n\",\n    \"print(len(df))\\n\",\n    \"add = int(len(df)/50)\\n\",\n    \"print(add)\\n\",\n    \"for p in pair1:\\n\",\n    \"    if p[0] == \\\"solubility expressed as a logarithm in mol/L\\\":\\n\",\n    \"        ran = random.sample(range(0,927), 18)\\n\",\n    \"        for i, df_slice in enumerate(df.iterrows()):\\n\",\n    \"            if i in ran:\\n\",\n    \"                tmp_dict = {}\\n\",\n    \"                question = random_generate_4(p)\\n\",\n    \"                output = \\\" Unable to answer the question due to lack of conditions\\\\n\\\"\\n\",\n    \"                tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"                tmp_dict[\\\"input\\\"] = \\\" \\\"+str(df_slice[1][slot[p[1]]])+\\\"\\\\n\\\"\\n\",\n    \"                tmp_dict[\\\"output\\\"] = output\\n\",\n    \"                data_list.append(tmp_dict)\\n\",\n    \"print(len(data_list))\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 10,\n   \"id\": \"7563850d\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"30\\n\",\n      \"['typhoon', 'iran', 'freckle', 'rhythm', 'slip', 'love', 'draw', 'pediatrician', 'temple', 'description']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('../2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\\n\",\n    \"# add no-answer question according to original length of data_frame\\n\",\n    \"add = int(len(df)/30)\\n\",\n    \"print(add)\\n\",\n    \"add_nouns = random.sample(nouns, add)\\n\",\n    \"print(add_nouns[:10])\\n\",\n    \"# input is an \\n\",\n    \"# output: an does not have p[0]\\n\",\n    \"for an in add_nouns:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran1 = random.randint(0,1)\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        ran2 = random.randint(0,6)\\n\",\n    \"        p = pair1[ran2]\\n\",\n    \"        if p[0] == \\\"solubility expressed as a logarithm in mol/L\\\":\\n\",\n    \"            question, output = random_generate_1(p, str(df_slice[1][slot[p[0]]]))\\n\",\n    \"            output = \\\" \\\"+an+\\\" does not have solubility.\\\\n\\\"\\n\",\n    \"        else:\\n\",\n    \"            question = random_generate_2(p)\\n\",\n    \"            output = \\\" \\\"+an+\\\" does not have \\\"+p[0]+\\\"\\\\n\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        ran2 = random.randint(0,1)\\n\",\n    \"        p = pair2[ran2]\\n\",\n    \"        question = random_generate_3(p)\\n\",\n    \"        output = \\\" \\\"+an+\\\" does not have \\\"+p[0]+\\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] =  \\\" \\\"+an+\\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = output\\n\",\n    \"    data_list.append(tmp_dict)\\n\",\n    \"\\n\",\n    \"random.shuffle(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 11,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"9372\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"print(len(data_list))\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('ESOL.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"ce1a9f8a\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.6.13\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/Emerging PV database/EPVDB.csv",
    "content": "Refs.,PCE [%],initial PCE [%],PCE after 200 h test [%],PCE after 100 h test [%],PCE after 1000 h test [%],average visible transmittance [%],Absorber,Absorber blend,Absorber material,Inorganic absorber material,Absorber perovskite,Active material,Bottom material bandgap [eV],Bottom active absorber material,Bottom absorber material,conditions of stability tests,Dye sensitizer,Energy yield in 200 h [Wh cm-2],Energy yield in 1000 h [Wh cm-2],Bandgap [eV],Top material bandgap of tandem solar cell  [eV],Bottom absorber material bandgap [eV],middle and top material bandgap of multijunction solar cell  [eV],fill factor [%],Jsc [mA cm−2],Luminophore and absorber material of solar cell with luminescent concentrator,middle and top absorber material of multijunction solar cell,middle and top absorber of multijunction solar cell,Sensitizing dye,Top absorber material of tandem solar cell,Top absorber of tandem solar cell,Voc [mV]\r\n\"T. Jiang, Z. Chen, X. Chen, T. Liu, X. Chen, W. E. I. Sha, H. Zhu, Y. Yang, Sol. RRL 2020, 4, 1900467.\",20.7,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.4,,,,,,,,,1.25,,,,80.2,30.6,,,,,,,843\r\n\"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\",20.4,,,,,,,,,,GuaSCN:(FASnI3)0.6(MAPbI3)0.4,,,,,,,,,1.26,,,,80.2,30.5,,,,,,,834\r\n\"C. Li, Z. Song, D. Zhao, C. Xiao, B. Subedi, N. Shrestha, M. M. Junda, C. Wang, C.-S. Jiang, M. Al-Jassim, R. J. Ellingson, N. J. Podraza, K. Zhu, Y. Yan, Adv. Energy Mater. 2019, 9, 1803135.\",19,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.34(MAPbBr3)0.06,,,,,,,,,1.26,,,,74.5,28.8,,,,,,,888\r\n\"R. Lin, K. Xiao, Z. Qin, Q. Han, C. Zhang, M. Wei, M. I. Saidaminov, Y. Gao, J. Xu, M. Xiao, A. Li, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2019, 4, 864.\",20.9,,,,,,,,,,MA0.3FA0.7Pb0.5Sn0.5I3,,,,,,,,,1.27,,,,80.5,31.4,,,,,,,827\r\n\"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\",20.3,,,,,,,,,,FA0.5MA0.45Cs0.05Pb0.5Sn0.5I3,,,,,,,,,1.28,,,,79.1,30.2,,,,,,,850\r\n\"G. Kapil, T. Bessho, C. H. Ng, K. Hamada, M. Pandey, M. A. Kamarudin, D. Hirotani, T. Kinoshita, T. Minemoto, Q. Shen, T. Toyoda, T. N. Murakami, H. Segawa, S. Hayase, ACS Energy Lett. 2019, 4, 1991.\",18.4,,,,,,,,,,Cs0.025FA0.475MA0.5Sn0.5Pb0.5I3,,,,,,,,,1.28,,,,72,32.8,,,,,,,780\r\n\"S. Shao, Y. Cui, H. Duim, X. Qiu, J. Dong, G. H. ten Brink, G. Portale, R. C. Chiechi, S. Zhang, J. Hou, M. A. Loi, Adv. Mater. 2018, 30, 1803703.\",16,,,,,,,,,,FASn0.5Pb0.5I3,,,,,,,,,1.29,,,,70.8,29.3,,,,,,,771\r\n\"T. S. Ripolles, D. Yamasuso, Y. Zhang, M. A. Kamarudin, C. Ding, D. Hirotani, Q. Shen, S. Hayase, J. Phys. Chem. C 2018, 122, 27284.\",15.9,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.3(MAPbBr3)0.1,,,,,,,,,1.29,,,,78,26.5,,,,,,,770\r\n\"M. Liu, Z. Chen, Z. Chen, H.-L. Yip, Y. Cao, Mater. Chem. Front. 2019, 3, 496.\",13.8,,,,,,,,,,FA0.5MA0.5Pb0.5Sn0.5I3,,,,,,,,,1.3,,,,72.1,29,,,,,,,660\r\n\"Y. Wang, J. Tu, T. Li, C. Tao, X. Deng, Z. Li, J. Mater. Chem. A 2019, 7, 7683.\",5,,,,,,,,,,CsSnI3,,,,,,,,,1.31,,,,50.3,23.8,,,,,,,420\r\n\"F. Li, C. Zhang, J.-H. Huang, H. Fan, H. Wang, P. Wang, C. Zhan, C.-M. Liu, X. Li, L.-M. Yang, Y. Song, K.-J. Jiang, Angew. Chem., Int. Ed. 2019, 58, 6688.\",7.1,,,,,,,,,,MASnI3,,,,,,,,,1.31,,,,64,22.9,,,,,,,486\r\n\"G. E. Eperon, T. Leijtens, K. A. Bush, R. Prasanna, T. Green, J. T.-W. Wang, D. P. McMeekin, G. Volonakis, R. L. Milot, R. May, A. Palmstrom, D. J. Slotcavage, R. A. Belisle, J. B. Patel, E. S. Parrott, R. J. Sutton, W. Ma, F. Moghadam, B. Conings, A. Babayigit, H.-G. Boyen, S. Bent, F. Giustino, L. M. Herz, M. B. Johnston, M. D. McGehee, H. J. Snaith, Science 2016, 354, 861.\",14.1,,,,,,,,,,FA0.75Cs0.25Sn0.5Pb0.5I3,,,,,,,,,1.31,,,,71.4,26.7,,,,,,,740\r\n\"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\",11.6,,,,,,,,,,MAPb0.4Sn0.6I2.8Br0.2,,,,,,,,,1.32,,,,68.9,23.4,,,,,,,720\r\n\"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. Gödel, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\",10,,,,,,,,,,MAPb0.4Sn0.6I3,,,,,,,,,1.34,,,,63.6,20.5,,,,,,,767\r\n\"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\",12.1,,,,,,,,,,MAPb0.4Sn0.6I2.6Br0.4,,,,,,,,,1.34,,,,75.1,20.7,,,,,,,780\r\n\"X. Lian, J. Chen, Y. Zhang, M. Qin, J. Li, S. Tian, W. Yang, X. Lu, G. Wu, H. Chen, Adv. Funct. Mater. 2019, 29, 1807024.\",16.3,,,,,,,,,,FAPb0.7Sn0.3I3,,,,,,,,,1.35,,,,79,26.5,,,,,,,780\r\n\"M. Zhang, D. Chi, J. Wang, F. Wu, S. Huang, Sol. Energy 2020, 201, 589.\",14.7,,,,,,,,,,FA0.3MA0.7Pb0.7Sn0.3I3,,,,,,,,,1.37,,,,73.6,27.1,,,,,,,737\r\n\"D. Chi, S. Huang, M. Zhang, S. Mu, Y. Zhao, Y. Chen, J. You, Adv. Funct. Mater. 2018, 28, 1804603.\",17.3,,,,,,,,,,FAPb0.75Sn0.25I3,,,,,,,,,1.38,,,,75.4,28.2,,,,,,,810\r\n\"H. L. Zhu, J. Xiao, J. Mao, H. Zhang, Y. Zhao, W. C. H. Choy, Adv. Funct. Mater. 2017, 27, 1605469.\",15.2,,,,,,,,,,MAPb0.75Sn0.25I3,,,,,,,,,1.38,,,,72.5,26.2,,,,,,,800\r\n\"X. Zhou, L. Zhang, X. Wang, C. Liu, S. Chen, M. Zhang, X. Li, W. Yi, B. Xu, Adv. Mater. 2020, 32, 1908107.\",20.6,,,,,,,,,,FA0.7MA0.3Pb0.7Sn0.3I3,,,,,,,,,1.39,,,,76,26.6,,,,,,,1020\r\n\"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. Gödel, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\",8.2,,,,,,,,,,MAPb0.6Sn0.4I3,,,,,,,,,1.4,,,,61.8,17.8,,,,,,,745\r\n\"P. Wang, F. Li, K.-J. Jiang, Y. Zhang, H. Fan, Y. Zhang, Y. Miao, J.-H. Huang, C. Gao, X. Zhou, F. Wang, L.-M. Yang, C. Zhan, Y. Song, Adv. Sci. 2020, 7, 1903047.\",7.8,,,,,,,,,,MASnI3,,,,,,,,,1.4,,,,66.2,20.7,,,,,,,570\r\n\"D. B. Khadka, Y. Shirai, M. Yanagida, K. Miyano, J. Mater. Chem. C 2020, 8, 2307.\",5.9,,,,,,,,,,FA1−xRbxSnI3,,,,,,,,,1.41,,,,60.6,20,,,,,,,487\r\n\"Z. Yang, A. Rajagopal, C.-C. Chueh, S. B. Jo, B. Liu, T. Zhao, A. K. Y. Jen, Adv. Mater. 2016, 28, 8990.\",14.4,,,,,,,,,,MAPb0.75Sn0.25I3,,,,,,,,,1.42,,,,78,22.4,,,,,,,820\r\n\"M. M. Tavakoli, S. M. Zakeeruddin, M. Grätzel, Z. Fan, Adv. Mater. 2018, 30, 1705998.\",10.4,,,,,,,,,,MAPb0.7Sn0.3I3,,,,,,,,,1.43,,,,66.4,20.3,,,,,,,772\r\n\"T. Wu, X. Liu, X. He, Y. Wang, X. Meng, T. Noda, X. Yang, L. Han, Sci. China Chem. 2020, 63, 107.\",10.2,,,,,,,,,,FASnI3,,,,,,,,,1.44,,,,74.7,21.6,,,,,,,630\r\n\"T. Wu, X. Liu, X. He, Y. Wang, X. Meng, T. Noda, X. Yang, L. Han, Sci. China Chem. 2020, 63, 107.\",9.4,,,,,,,,,,FASnI3,,,,,,,,,1.44,,,,73.4,21.1,,,,,,,606\r\n\"K. Nishimura, M. A. Kamarudin, D. Hirotani, K. Hamada, Q. Shen, S. Iikubo, T. Minemoto, K. Yoshino, S. Hayase, Nano Energy 2020, 74, 104858.\",13.2,,,,,,,,,,(FA0.9EA0.1)0.98EDA0.01SnI3,,,,,,,,,1.42,,,,78,20.3,,,,,,,840\r\n\"Y. Zhao, X. Xu, H. Zhang, J. Shi, L. Zhu, H. Wu, D. Li, Y. Luo, Q. Meng, J. Power Sources 2017, 359, 147.\",19.3,,,,,,,,,,FA0.6MA0.4PbI3,,,,,,,,,1.51,,,,77.5,23.8,,,,,,,1047\r\n\"S. Yuan, Y. Cai, S. Yang, H. Zhao, F. Qian, Y. Han, J. Sun, Z. Liu, S. Liu, Sol. RRL 2019, 3, 1900220.\",22,,,,,,,,,,FA0.85MA0.15PbI3,,,,,,,,,1.52,,,,78.6,24.9,,,,,,,1120\r\n\"H. Min, M. Kim, S.-U. Lee, H. Kim, G. Kim, K. Choi, J. H. Lee, S. I. Seok, Science 2019, 366, 749.\",23.7,,,,,,,,,,α-FAPbI3:MDACl2,,,,,,,,,1.53,,,,77.6,26.7,,,,,,,1144\r\n\"Q. Jiang, Y. Zhao, X. Zhang, X. Yang, Y. Chen, Z. Chu, Q. Ye, X. Li, Z. Yin, J. You, Nat. Photonics 2019, 13, 460.\",23.3,,,,,,,,,,FA1−xMAxPbI3,,,,,,,,,1.53,,,,78.4,25.2,,,,,,,1180\r\n\"T. Niu, J. Lu, M.-C. Tang, D. Barrit, D.-M. Smilgies, Z. Yang, J. Li, Y. Fan, T. Luo, I. McCulloch, A. Amassian, S. Liu, K. Zhao, Energy Environ. Sci. 2018, 11, 3358.\",18.6,,,,,,,,,,FAPbI3,,,,,,,,,1.53,,,,73.5,24.1,,,,,,,1050\r\n\"D. Yang, R. Yang, K. Wang, C. Wu, X. Zhu, J. Feng, X. Ren, G. Fang, S. Priya, S. Liu, Nat. Commun. 2018, 9, 3239.\",21.6,,,,,,,,,,FA0.95Cs0.05PbI3,,,,,,,,,1.53,,,,79.2,24.6,,,,,,,1110\r\n\"M. Jeong, I. W. Choi, E. M. Go, Y. Cho, M. Kim, B. Lee, S. Jeong, Y. Jo, H. W. Choi, J. Lee, J.-H. Bae, S. K. Kwak, D. S. Kim, C. Yang, Science 2020, 369, 1615.\",24.6,,,,,,,,,,FAPbI3,,,,,,,,,1.54,,,,79.6,26.2,,,,,,,1181\r\n\"W. S. Yang, B.-W. Park, E. H. Jung, N. J. Jeon, Y. C. Kim, D. U. Lee, S. S. Shin, J. Seo, E. K. Kim, J. H. Noh, S. I. Seok, Science 2017, 356, 1376.\",22.1,,,,,,,,,,(FAPbI3)0.9(MAPbBr3)0.1,,,,,,,,,1.54,,,,80.3,25,,,,,,,1105\r\n\"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\",21.5,,,,,,,,,,Cs0.05FA0.70MA0.25PbI3-DAP,,,,,,,,,1.55,,,,79.2,23.4,,,,,,,1160\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\",25.2,,,,,,,,,, ,,,,,,,,,1.56,,,,84.8,24.1,,,,,,,1180\r\n\"E. H. Jung, N. J. Jeon, E. Y. Park, C. S. Moon, T. J. Shin, T.-Y. Yang, J. H. Noh, J. Seo, Nature 2019, 567, 511.\",22.7,,,,,,,,,,(FAPbI3)0.95(MAPbBr3)0.05,,,,,,,,,1.56,,,,79.9,24.9,,,,,,,1145\r\n\"Q. Jiang, Z. Chu, P. Wang, X. Yang, H. Liu, Y. Wang, Z. Yin, J. Wu, X. Zhang, J. You, Adv. Mater. 2017, 29, 1703852.\",20.9,,,,,,,,,,(FAPbI3)1−x(MAPbBr3)x,,,,,,,,,1.56,,,,78,24,,,,,,,1116\r\n\"Z. Chen, X. Zheng, F. Yao, J. Ma, C. Tao, G. Fang, J. Mater. Chem. A 2018, 6, 17625.\",19.7,,,,,,,,,,(MA0.7FA0.3)0.97EDA0.015PbI3,,,,,,,,,1.56,,,,77.3,23.7,,,,,,,1075\r\n\"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\",23,,,,,,,,,,Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3,,,,,,,,,1.57,,,,81.6,24.1,,,,,,,1170\r\n\"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\",22.3,,,,,,,,,,Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3,,,,,,,,,1.57,,,,82,23.8,,,,,,,1143\r\n\"L. Meng, C. Sun, R. Wang, W. Huang, Z. Zhao, P. Sun, T. Huang, J. Xue, J.-W. Lee, C. Zhu, Y. Huang, Y. Li, Y. Yang, J. Am. Chem. Soc. 2018, 140, 17255.\",20.6,,,,,,,,,,(FAPbI3)1−x(MAPbBr3)x,,,,,,,,,1.57,,,,80.5,22.8,,,,,,,1120\r\n\"J. J. Yoo, S. Wieghold, M. C. Sponseller, M. R. Chua, S. N. Bertram, N. T. P. Hartono, J. S. Tresback, E. C. Hansen, J.-P. Correa-Baena, V. Bulović, T. Buonassisi, S. S. Shin, M. G. Bawendi, Energy Environ. Sci. 2019, 12, 2192.\",22.6,,,,,,,,,,(FAPbI3)0.92(MAPbBr3)0.08,,,,,,,,,1.58,,,,78.6,24.2,,,,,,,1186\r\n\"H. B. Lee, N. Kumar, M. M. Ovhal, Y. J. Kim, Y. M. Song, J.-W. Kang, Adv. Funct. Mater. 2020, 30, 2001559.\",20.4,,,,,,,,,,Cs0.05(FAPbI3)0.85(MAPbBr3)0.15,,,,,,,,,1.58,,,,77.8,23.3,,,,,,,1125\r\n\"P. Cui, D. Wei, J. Ji, H. Huang, E. Jia, S. Dou, T. Wang, W. Wang, M. Li, Nat. Energy 2019, 4, 150.\",21.9,,,,,,,,,,FA0.15MA0.85PbI3,,,,,,,,,1.58,,,,80.6,24.2,,,,,,,1120\r\n\"M. Li, Z.-K. Wang, M.-P. Zhuo, Y. Hu, K.-H. Hu, Q.-Q. Ye, S. M. Jain, Y.-G. Yang, X.-Y. Gao, L.-S. Liao, Adv. Mater. 2018, 30, 1800258.\",21.1,,,,,,,,,,MAPb0.9Sn0.05Cu0.05I2.9Br0.1,,,,,,,,,1.59,,,,81,24,,,,,,,1086\r\n\"X. Zheng, B. Chen, J. Dai, Y. Fang, Y. Bai, Y. Lin, H. Wei, X. C. Zeng, J. Huang, Nat. Energy 2017, 2, 17102.\",21,,,,,,,,,,FA0.85MA0.15Pb(I0.85Br0.15)3,,,,,,,,,1.59,,,,77.7,23.7,,,,,,,1140\r\n\"L. Wang, H. Zhou, J. Hu, B. Huang, M. Sun, B. Dong, G. Zheng, Y. Huang, Y. Chen, L. Li, Z. Xu, N. Li, Z. Liu, Q. Chen, L.-D. Sun, C.-H. Yan, Science 2019, 363, 265.\",20.3,,,,,,,,,,MAPbI3−xClx,,,,,,,,,1.6,,,,77.4,23.2,,,,,,,1130\r\n\"P. Cui, D. Wei, J. Ji, H. Huang, E. Jia, S. Dou, T. Wang, W. Wang, M. Li, Nat. Energy 2019, 4, 150.\",20.5,,,,,,,,,,MAPbI3,,,,,,,,,1.61,,,,73.5,25.1,,,,,,,1110\r\n\"X. Zhao, C. Yao, T. Liu, J. C. Hamill Jr., G. O. Ngongang Ndjawa, G. Cheng, N. Yao, H. Meng, Y.-L. Loo, Adv. Mater. 2019, 31, 1904494.\",21.6,,,,,,,,,,Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3,,,,,,,,,1.61,,,,76.1,24.9,,,,,,,1140\r\n\"M. A. Mahmud, T. Duong, Y. Yin, H. T. Pham, D. Walter, J. Peng, Y. Wu, L. Li, H. Shen, N. Wu, N. Mozaffari, G. Andersson, K. R. Catchpole, K. J. Weber, T. P. White, Adv. Funct. Mater. 2020, 30, 1907962.\",22.6,,,,,,,,,,Cs0.07Rb0.03FA0.765MA0.135PbI2.55Br0.45,,,,,,,,,1.61,,,,78.5,24,,,,,,,1200\r\n\"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\",21.7,,,,,,,,,,MAPbI3-DAP,,,,,,,,,1.62,,,,81.7,22.5,,,,,,,1180\r\n\"K. Choi, J. Lee, H. I. Kim, C. W. Park, G.-W. Kim, H. Choi, S. Park, S. A. Park, T. Park, Energy Environ. Sci. 2018, 11, 3238.\",20.3,,,,,,,,,,Cs0.05FA0.76MA0.19PbBr0.6I2.4,,,,,,,,,1.63,,,,76.8,23.4,,,,,,,1130\r\n\"X. Zhao, C. Yao, T. Liu, J. C. Hamill Jr., G. O. Ngongang Ndjawa, G. Cheng, N. Yao, H. Meng, Y.-L. Loo, Adv. Mater. 2019, 31, 1904494.\",20.4,,,,,,,,,,Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3,,,,,,,,,1.64,,,,75.8,23.6,,,,,,,1140\r\n\"N. J. Jeon, J. H. Noh, Y. C. Kim, W. S. Yang, S. Ryu, S. I. Seok, Nat. Mater. 2014, 13, 897.\",16.2,,,,,,,,,,MAPbI1−xBrx,,,,,,,,,1.65,,,,74.2,19.6,,,,,,,1109\r\n\"J. H. Noh, S. H. Im, J. H. Heo, T. N. Mandal, S. I. Seok, Nano Lett. 2013, 13, 1764.\",10.4,,,,,,,,,,MAPb(I0.87Br0.13)3,,,,,,,,,1.66,,,,70.4,16.3,,,,,,,904\r\n\"S. A. Kulkarni, T. Baikie, P. P. Boix, N. Yantara, N. Mathews, S. Mhaisalkar, J. Mater. Chem. A 2014, 2, 9221.\",8.2,,,,,,,,,,MAPb(I0.88Br0.12)3,,,,,,,,,1.67,,,,65.8,13.9,,,,,,,890\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",20.7,,,,,,,,,,Cs0.05MA0.15FA0.8Pb(I0.75Br0.25)3,,,,,,,,,1.68,,,,79.7,21.3,,,,,,,1220\r\n\"M. Chen, M.-G. Ju, H. F. Garces, A. D. Carl, L. K. Ono, Z. Hawash, Y. Zhang, T. Shen, Y. Qi, R. L. Grimm, D. Pacifici, X. C. Zeng, Y. Zhou, N. P. Padture, Nat. Commun. 2019, 10, 16.\",7.1,,,,,,,,,,MAPb(I0.74Br0.26)3,,,,,,,,,1.69,,,,63,10.4,,,,,,,936\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",16.9,,,,,,,,,,Cs0.2FA0.8Pb(I0.75Br0.25)3,,,,,,,,,1.7,,,,71.5,20.2,,,,,,,1170\r\n\"M.-J. Wu, C.-C. Kuo, L.-S. Jhuang, P.-H. Chen, Y.-F. Lai, F.-C. Chen, Adv. Energy Mater. 2019, 9, 1901863.\",12.5,,,,,,,,,,MA0.85Cs0.15Pb(I0.85Br0.15)3,,,,,,,,,1.71,,,,75.5,15.4,,,,,,,1070\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",18.6,,,,,,,,,,FA0.17Cs0.83PbI2.2Br0.8,,,,,,,,,1.72,,,,77.9,19.2,,,,,,,1244\r\n\"D. P. McMeekin, G. Sadoughi, W. Rehman, G. E. Eperon, M. Saliba, M. T. Hörantner, A. Haghighirad, N. Sakai, L. Korte, B. Rech, M. B. Johnston, L. M. Herz, H. J. Snaith, Science 2016, 351, 151.\",17.1,,,,,,,,,,FA0.83Cs0.17Pb(I0.6Br0.4)3,,,,,,,,,1.72,,,,73.5,19.4,,,,,,,1200\r\n\"T. Duong, H. Pham, T. C. Kho, P. Phang, K. C. Fong, D. Yan, Y. Yin, J. Peng, M. A. Mahmud, S. Gharibzadeh, B. A. Nejand, I. M. Hossain, M. R. Khan, N. Mozaffari, Y. Wu, H. Shen, J. Zheng, H. Mai, W. Liang, C. Samundsett, M. Stocks, K. McIntosh, G. G. Andersson, U. Lemmer, B. S. Richards, U. W. Paetzold, A. Ho-Ballie, Y. Liu, D. Macdonald, A. Blakers, J. Wong-Leung, T. White, K. Weber, K. Catchpole, Adv. Energy Mater. 2020, 10, 1903553.\",18.3,,,,,,,,,,Rb0.05Cs0.095MA0.1425FA0.7125PbI2Br,,,,,,,,,1.74,,,,76.3,18.9,,,,,,,1269\r\n\"S. Gharibzadeh, B. Abdollahi Nejand, M. Jakoby, T. Abzieher, D. Hauschild, S. Moghadamzadeh, J. A. Schwenzer, P. Brenner, R. Schmager, A. A. Haghighirad, L. Weinhardt, U. Lemmer, B. S. Richards, I. A. Howard, U. W. Paetzold, Adv. Energy Mater. 2019, 9, 1803699.\",19.8,,,,,,,,,,FA0.83Cs0.17Pb(I0.6Br0.4)3,,,,,,,,,1.75,,,,78,19.4,,,,,,,1310\r\n\"Y. Lin, B. Chen, F. Zhao, X. Zheng, Y. Deng, Y. Shao, Y. Fang, Y. Bai, C. Wang, J. Huang, Adv. Mater. 2017, 29, 1700607.\",18.5,,,,,,,,,,(FA0.83MA0.17)0.95Cs0.05Pb(I0.6Br0.4)3,,,,,,,,,1.76,,,,76.4,20,,,,,,,1210\r\n\"Q. Ye, Y. Zhao, S. Mu, F. Ma, F. Gao, Z. Chu, Z. Yin, P. Gao, X. Zhang, J. You, Adv. Mater. 2019, 31, 1905143.\",18.6,,,,,,,,,,CsPbI3−xBrx,,,,,,,,,1.77,,,,82.5,18.3,,,,,,,1234\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",15.7,,,,,,,,,,Cs0.17FA0.83Pb(I0.6Br0.4)3,,,,,,,,,1.78,,,,70.5,18.4,,,,,,,1210\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",19,,,,,,,,,,Cs0.12MA0.05FA0.83Pb(I0.6Br0.4)3,,,,,,,,,1.79,,,,80,19,,,,,,,1250\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",16.5,,,,,,,,,,FA0.17Cs0.83PbI1.8Br1.2,,,,,,,,,1.79,,,,74.8,17.2,,,,,,,1284\r\n\"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\",13.7,,,,,,,,,,MAPbBrI2,,,,,,,,,1.8,,,,75,14.4,,,,,,,1272\r\n\"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\",16.3,,,,,,,,,,FA0.6Cs0.4Pb(I0.65Br0.35)3,,,,,,,,,1.81,,,,78.6,17,,,,,,,1220\r\n\"Y.-N. Zhang, B. Li, L. Fu, Y. Zou, Q. Li, L.-W. Yin, Sol. Energy Mater. Sol. Cells 2019, 194, 168.\",17.1,,,,,,,,,,FAPbI1.5Br1.5/CsPbI1.5Br1.5,,,,,,,,,1.82,,,,74,21,,,,,,,1100\r\n\"M. Chen, M.-G. Ju, A. D. Carl, Y. Zong, R. L. Grimm, J. Gu, X. C. Zeng, Y. Zhou, N. P. Padture, Joule 2018, 2, 558.\",3.3,,,,,,,,,,Cs2TiBr6,,,,,,,,,1.83,,,,56.9,5.7,,,,,,,1020\r\n\"M.-J. Wu, C.-C. Kuo, L.-S. Jhuang, P.-H. Chen, Y.-F. Lai, F.-C. Chen, Adv. Energy Mater. 2019, 9, 1901863.\",8.6,,,,,,,,,,MA0.85Cs0.15Pb(I0.65Br0.35)3,,,,,,,,,1.83,,,,68.4,11.3,,,,,,,1110\r\n\"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\",15.2,,,,,,,,,,Cs0.2FA0.8Pb(I0.6Br0.4)3-DAP,,,,,,,,,1.84,,,,77.3,15.6,,,,,,,1260\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",15,,,,,,,,,,FA0.17Cs0.83PbI1.5Br1.5,,,,,,,,,1.85,,,,74.2,15.6,,,,,,,1296\r\n\"J. Zhang, Z. Wang, A. Mishra, M. Yu, M. Shasti, W. Tress, D. J. Kubicki, C. E. Avalos, H. Lu, Y. Liu, B. I. Carlsen, A. Agarwalla, Z. Wang, W. Xiang, L. Emsley, Z. Zhang, M. Grätzel, W. Guo, A. Hagfeldt, Joule 2020, 4, 222.\",17,,,,,,,,,,CsPb(I0.75Br0.25)3-0.5FAOAc,,,,,,,,,1.86,,,,79.8,15.9,,,,,,,1340\r\n\"W. Xiang, Z. Wang, D. J. Kubicki, X. Wang, W. Tress, J. Luo, J. Zhang, A. Hofstetter, L. Zhang, L. Emsley, M. Grätzel, A. Hagfeldt, Nat. Commun. 2019, 10, 4686.\",14,,,,,,,,,,CsPb0.8Ba0.2I2Br,,,,,,,,,1.87,,,,78.1,14,,,,,,,1280\r\n\"W. Xiang, Z. Wang, D. J. Kubicki, W. Tress, J. Luo, D. Prochowicz, S. Akin, L. Emsley, J. Zhou, G. Dietler, M. Grätzel, A. Hagfeldt, Joule 2019, 3, 205.\",13.7,,,,,,,,,,CsPb0.95Eu0.05I2Br,,,,,,,,,1.87,,,,76.8,14.6,,,,,,,1220\r\n\"S. Yang, H. Zhao, Y. Han, C. Duan, Z. Liu, S. Liu, Small 2019, 15, 1904387.\",15.3,,,,,,,,,,CsPbI2Br,,,,,,,,,1.88,,,,79,15.4,,,,,,,1250\r\n\"H. Zhao, Y. Han, Z. Xu, C. Duan, S. Yang, S. Yuan, Z. Yang, Z. Liu, S. Liu, Adv. Energy Mater. 2019, 9, 1902279.\",15.6,,,,,,,,,,CsPbI2−xBr(A x,,,,,,,,,1.89,,,,78.3,15.3,,,,,,,1300\r\n\"C. Duan, J. Cui, M. Zhang, Y. Han, S. Yang, H. Zhao, H. Bian, J. Yao, K. Zhao, Z. Liu, S. Liu, Adv. Energy Mater. 2020, 10, 2000691.\",16.1,,,,,,,,,,CsPbI2Br,,,,,,,,,1.9,,,,79.7,15.3,,,,,,,1320\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",14.4,,,,,,,,,,FA0.17Cs0.83PbI1.2Br1.8,,,,,,,,,1.91,,,,70.1,15.6,,,,,,,1312\r\n\"H. Bian, D. Bai, Z. Jin, K. Wang, L. Liang, H. Wang, J. Zhang, Q. Wang, S. Liu, Joule 2018, 2, 1500.\",13.5,,,,,,,,,,CsPbI2Br,,,,,,,,,1.91,,,,79.9,14.3,,,,,,,1177\r\n\"K. M. Boopathi, P. Karuppuswamy, A. Singh, C. Hanmandlu, L. Lin, S. A. Abbas, C. C. Chang, P. C. Wang, G. Li, C. W. Chu, J. Mater. Chem. A 2017, 5, 20843.\",2,,,,,,,,,,MA3Sb2I9+HI,,,,,,,,,1.91,,,,60.8,5.4,,,,,,,620\r\n\"I. Turkevych, S. Kazaoui, E. Ito, T. Urano, K. Yamada, H. Tomiyasu, H. Yamagishi, M. Kondo, S. Aramaki, ChemSusChem 2017, 10, 3754.\",4.3,,,,,,,,,,Ag3BiI6,,,,,,,,,1.94,,,,63.8,10.7,,,,,,,630\r\n\"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\",2.2,,,,,,,,,,AgBiI4,,,,,,,,,1.94,,,,62.7,5.2,,,,,,,670\r\n\"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\",2.6,,,,,,,,,,AgBiI5,,,,,,,,,1.95,,,,62.4,6,,,,,,,690\r\n\"B.-W. Park, B. Philippe, X. Zhang, H. Rensmo, G. Boschloo, E. M. J. Johansson, Adv. Mater. 2015, 27, 6806.\",1.1,,,,,,,,,,Cs3Bi2I9,,,,,,,,,1.97,,,,59.6,2.2,,,,,,,850\r\n\"J. Liang, P. Zhao, C. Wang, Y. Wang, Y. Hu, G. Zhu, L. Ma, J. Liu, Z. Jin, J. Am. Chem. Soc. 2017, 139, 14009.\",8.3,,,,,,,,,,CsPbIBr2,,,,,,,,,1.98,,,,62,12.3,,,,,,,1080\r\n\"D. Forgács, L. Gil-Escrig, D. Pérez-Del-Rey, C. Momblona, J. Werner, B. Niesen, C. Ballif, M. Sessolo, H. J. Bolink, Adv. Energy Mater. 2017, 7, 1602121.\",9.6,,,,,,,,,,Cs0.15FA0.85Pb(I0.3Br0.7)3,,,,,,,,,2,,,,72.3,11.2,,,,,,,1185\r\n\"S. A. Kulkarni, T. Baikie, P. P. Boix, N. Yantara, N. Mathews, S. Mhaisalkar, J. Mater. Chem. A 2014, 2, 9221.\",2.8,,,,,,,,,,MAPb(I0.41Br0.59)3,,,,,,,,,2.03,,,,52.7,6.4,,,,,,,836\r\n\"Q. Xue, G. Chen, M. Liu, J. Xiao, Z. Chen, Z. Hu, X.-F. Jiang, B. Zhang, F. Huang, W. Yang, H.-L. Yip, Y. Cao, Adv. Energy Mater. 2016, 6, 1502021.\",10.3,,,,,,,,,,MAPb(I0.3Br0.7)xCl3−x(Br),,,,,,,,,2.04,,,,79.2,9.7,,,,,,,1340\r\n\"Y. Zhao, A. M. Nardes, K. Zhu, Faraday Discuss. 2014, 176, 301.\",6.1,,,,,,,,,,MAPbIBr2,,,,,,,,,2.05,,,,77.1,5.4,,,,,,,1450\r\n\"H. Wang, S. Cao, B. Yang, H. Li, M. Wang, X. Hu, K. Sun, Z. Zang, Sol. RRL 2020, 4, 1900363.\",10.2,,,,,,,,,,CsPbIBr2,,,,,,,,,2.09,,,,69.4,11.5,,,,,,,1270\r\n\"W. Zhu, Z. Zhang, W. Chai, Q. Zhang, D. Chen, Z. Lin, J. Chang, J. Zhang, C. Zhang, Y. Hao, ChemSusChem 2019, 12, 2318.\",10.7,,,,,,,,,,CsPbIBr2,,,,,,,,,2.1,,,,72,11.8,,,,,,,1261\r\n\"B. Zhang, W. Bi, Y. Wu, C. Chen, H. Li, Z. Song, Q. Dai, L. Xu, H. Song, ACS Appl. Mater. Interfaces 2019, 11, 33868.\",9.2,,,,,,,,,,GAI-DEE-CsPbIBr2,,,,,,,,,2.11,,,,74.6,10.2,,,,,,,1200\r\n\"R. Nie, A. Mehta, B.-w. Park, H.-W. Kwon, J. Im, S. I. Seok, J. Am. Chem. Soc. 2018, 140, 872.\",3.1,,,,,,,,,,MASbSI2,,,,,,,,,2.14,,,,58.4,8.1,,,,,,,650\r\n\"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\",4.4,,,,,,,,,,(FA0.85MA0.15Pb(I0.85Br0.15)3) R = 0.7,,,,,,,,,2.15,,,,64.8,6.3,,,,,,,1084\r\n\"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\",2,,,,,,,,,,(FA0.85MA0.15Pb(I0.85Br0.15)3) R = 0.56,,,,,,,,,2.19,,,,69.5,3,,,,,,,1051\r\n\"F. Umar, J. Zhang, Z. Jin, I. Muhammad, X. Yang, H. Deng, K. Jahangeer, Q. Hu, H. Song, J. Tang, Adv. Opt. Mater. 2019, 7, 1801368.\",1.2,,,,,,,,,,Cs3Sb2I9,,,,,,,,,2.2,,,,55.9,3.6,,,,,,,610\r\n\"Y. Zhang, Y. Liang, Y. Wang, F. Guo, L. Sun, D. Xu, ACS Energy Lett. 2018, 3, 1808.\",10.6,,,,,,,,,,FAPbBr3,,,,,,,,,2.27,,,,76.5,8.9,,,,,,,1552\r\n\"J. Duan, Y. Zhao, B. He, Q. Tang, Angew. Chem., Int. Ed. 2018, 57, 3787.\",9.7,,,,,,,,,,CsPbBr3,,,,,,,,,2.31,,,,81.9,8.12,,,,,,,1458\r\n\"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\",10.1,,,,,,,,,,MAPbBr3,,,,,,,,,2.32,,,,79.1,7.72,,,,,,,1653\r\n\"G. Liao, J. Duan, Y. Zhao, Q. Tang, Sol. Energy 2018, 171, 279.\",8.2,,,,,,,,,,CsPbBr3,,,,,,,,,2.33,,,,76.1,7.3,,,,,,,1470\r\n\"J. Zhu, B. He, Z. Gong, Y. Ding, W. Zhang, X. Li, Z. Zong, H. Chen, Q. Tang, ChemSusChem 2020, 13, 1834.\",9.7,,,,,,,,,,CsPbBr3,,,,,,,,,2.34,,,,82.8,7.4,,,,,,,1584\r\n\"Y. Zhao, J. Duan, Y. Wang, X. Yang, Q. Tang, Nano Energy 2020, 67, 104286.\",10.7,,,,,,,,,,CsPbBr3,,,,,,,,,2.35,,,,83.5,7.9,,,,,,,1622\r\n\"Y. Zhao, J. Duan, H. Yuan, Y. Wang, X. Yang, B. He, Q. Tang, Sol. RRL 2019, 3, 1800284.\",10.6,,,,,,,,,,CsSnBr3,,,,,,,,,2.35,,,,84.4,7.8,,,,,,,1610\r\n\"C. H. Ng, T. S. Ripolles, K. Hamada, S. H. Teo, H. N. Lim, J. Bisquert, S. Hayase, Sci. Rep. 2018, 8, 2482.\",4,,,,,,,,,,CsPbBr2.9I0.1,,,,,,,,,2.36,,,,63.6,5.5,,,,,,,1130\r\n\"F. Jiang, D. Yang, Y. Jiang, T. Liu, X. Zhao, Y. Ming, B. Luo, F. Qin, J. Fan, H. Han, L. Zhang, Y. Zhou, J. Am. Chem. Soc. 2018, 140, 1019.\",2.2,,,,,,,,,,MA3Sb2ClxI9−x,,,,,,,,,2.37,,,,63.5,5,,,,,,,690\r\n\"X. Wan, Z. Yu, W. Tian, F. Huang, S. Jin, X. Yang, Y.-B. Cheng, A. Hagfeldt, L. Sun, J. Energy Chem. 2020, 46, 8.\",8.1,,,,,,,,,,CsPbBr3,,,,,,,,,2.38,,,,78.8,6.9,,,,,,,1490\r\n\"Y. Zhao, H. Xu, Y. Wang, X. Yang, J. Duan, Q. Tang, J. Power Sources 2019, 440, 227151.\",10.3,,,,,,,,,,Cs0.91Rb0.09PbBr3,,,,,,,,,2.39,,,,80,8.2,,,,,,,1580\r\n\"M. Safdari, P. H. Svensson, M. T. Hoang, I. Oh, L. Kloo, J. M. Gardner, J. Mater. Chem. A 2016, 4, 15638.\",1.1,,,,,,,,,,BdAPbI4,,,,,,,,,2.42,,,,43,2.9,,,,,,,870\r\n\"G. Murugadoss, R. Thangamuthu, S. M. Senthil Kumar, N. Anandhan, M. Rajesh Kumar, A. Rathishkumar, J. Alloys Compd. 2019, 787, 17.\",2.8,,,,,,,,,,CsPb2Br5,,,,,,,,,2.43,,,,60.3,5.7,,,,,,,820\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",2.4,,,,,,,,,,FAPbBr2.1Cl0.9,,,,,,,,,2.44,,,,60.9,3.4,,,,,,,1140\r\n\"E. Greul, M. L. Petrus, A. Binek, P. Docampo, T. Bein, J. Mater. Chem. A 2017, 5, 19972.\",1.7,,,,,,,,,,Cs2AgBiBr6,,,,,,,,,2.46,,,,40.2,3.9,,,,,,,1060\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",1.4,,,,,,,,,,FAPbBr2Cl,,,,,,,,,2.48,,,,52,2.5,,,,,,,1060\r\n\"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\",10.6,,,,,,,PTB7-Th:IEICO-4F,,,,,,,,,,,,1.32,,,,63.2,24.3,,,,,,,690\r\n\"X. Song, N. Gasparini, L. Ye, H. Yao, J. Hou, H. Ade, D. Baran, ACS Energy Lett. 2018, 3, 669.\",12.8,,,,,,,PTB7-Th:IEICO-4F,,,,,,,,,,,,1.34,,,,65.9,27.3,,,,,,,712\r\n\"X. Song, N. Gasparini, M. M. Nahid, S. H. K. Paleti, C. Li, W. Li, H. Ade, D. Baran, Adv. Funct. Mater. 2019, 29, 1902441.\",9.7,,,,,,,PBDTT-DPP:IEICO-4F,,,,,,,,,,,,1.34,,,,70.2,19.8,,,,,,,695\r\n\"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\",14.3,,,,,,,PBDB-T-2Cl:BTP-4F:PC61BM,,,,,,,,,,,,1.35,,,,66.5,26.8,,,,,,,802\r\n\"S. Liu, J. Yuan, W. Deng, M. Luo, Y. Xie, Q. Liang, Y. Zou, Z. He, H. Wu, Y. Cao, Nat. Photonics 2020, 14, 300.\",15.9,,,,,,,PM6:Y11,,,,,,,,,,,,1.36,,,,74.1,25.4,,,,,,,846\r\n\"J. Yuan, Y. Zhang, L. Zhou, G. Zhang, H.-L. Yip, T.-K. Lau, X. Lu, C. Zhu, H. Peng, P. A. Johnson, M. Leclerc, Y. Cao, J. Ulanski, Y. Li, Y. Zou, Joule 2019, 3, 1140.\",13.6,,,,,,,PM6:Y6,,,,,,,,,,,,1.37,,,,62.6,26.5,,,,,,,820\r\n\"Y. Cui, H. Yao, J. Zhang, K. Xian, T. Zhang, L. Hong, Y. Wang, Y. Xu, K. Ma, C. An, C. He, Z. Wei, F. Gao, J. Hou, Adv. Mater. 2020, 32, 1908205.\",17.3,,,,,,,PBDB-TF:BTP-eC9,,,,,,,,,,,,1.38,,,,78.5,26.2,,,,,,,841\r\n\"Q. Liu, Y. Jiang, K. Jin, J. Qin, J. Xu, W. Li, J. Xiong, J. Liu, Z. Xiao, K. Sun, S. Yang, X. Zhang, L. Ding, Sci. Bull. 2020, 65, 272.\",18.2,,,,,,,D18:Y6,,,,,,,,,,,,1.39,,,,76.6,27.7,,,,,,,859\r\n\"Y. Cui, H. Yao, L. Hong, T. Zhang, Y. Tang, B. Lin, K. Xian, B. Gao, C. An, P. Bi, W. Ma, J. Hou, Natl. Sci. Rev. 2019, 7, 1239.\",17,,,,,,,PBDB-TF:BTP-4Cl-12,,,,,,,,,,,,1.39,,,,25.5,77.6,,,,,,,858\r\n\"Z. Zhou, W. Liu, G. Zhou, M. Zhang, D. Qian, J. Zhang, S. Chen, S. Xu, C. Yang, F. Gao, H. Zhu, F. Liu, X. Zhu, Adv. Mater. 2020, 32, 1906324.\",16.6,,,,,,,PBDB-TF:AQx-2,,,,,,,,,,,,1.39,,,,76.3,25.4,,,,,,,860\r\n\"Y. Lin, B. Adilbekova, Y. Firdaus, E. Yengel, H. Faber, M. Sajjad, X. Zheng, E. Yarali, A. Seitkhan, O. M. Bakr, A. El-Labban, U. Schwingenschlögl, V. Tung, I. McCulloch, F. Laquai, T. D. Anthopoulos, Adv. Mater. 2019, 31, 1902965.\",17,,,,,,,PBDB-T-2F:Y6:PC71BM,,,,,,,,,,,,1.4,,,,77.8,26,,,,,,,840\r\n\"L. Liu, Y. Kan, K. Gao, J. Wang, M. Zhao, H. Chen, C. Zhao, T. Jiu, A.-K.-Y. Jen, Y. Li, Adv. Mater. 2020, 32, 1907604.\",17.1,,,,,,,PM6:Y6,,,,,,,,,,,,1.4,,,,77.6,26.4,,,,,,,834\r\n\"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\",16.5,,,,,,,PBDB-TF:BTP-4Cl,,,,,,,,,,,,1.4,,,,75,25.4,,,,,,,867\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\",17.4,,,,,,, ,,,,,,,,,,,,1.41,,,,77.9,25.8,,,,,,,862\r\n\"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\",15.6,,,,,,,PBDB-TF:BTP-4F,,,,,,,,,,,,1.42,,,,75.1,24.9,,,,,,,834\r\n\"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\",15.6,,,,,,, ,,,,,,,,,,,,1.42,,,,74.4,25,,,,,,,838\r\n\"Q. Guo, J. Lin, H. Liu, X. Dong, X. Guo, L. Ye, Z. Ma, Z. Tang, H. Ade, M. Zhang, Y. Li, Nano Energy 2020, 74, 104861.\",14.3,,,,,,,PM6:IDST-4F,,,,,,,,,,,,1.43,,,,70,24.9,,,,,,,820\r\n\"H. Lai, Q. Zhao, Z. Chen, H. Chen, P. Chao, Y. Zhu, Y. Lang, N. Zhen, D. Mo, Y. Zhang, F. He, Joule 2020, 4, 688.\",13.6,,,,,,,PBDB-TF:BTIC-F-m,,,,,,,,,,,,1.44,,,,69.1,21.4,,,,,,,920\r\n\"K. Jiang, Q. Wei, J. Y. L. Lai, Z. Peng, H. K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Joule 2019, 3, 3020.\",12.9,,,,,,,PM6:N-C11,,,,,,,,,,,,1.46,,,,70.6,21.5,,,,,,,852\r\n\"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\",14.6,,,,,,,PBDB-T-2Cl:BP-4F:MF1,,,,,,,,,,,,1.47,,,,71.7,23.1,,,,,,,882\r\n\"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\",12.4,,,,,,,PBDB-T:IDT-EDOT:PC71BM,,,,,,,,,,,,1.48,,,,67.7,20.8,,,,,,,880\r\n\"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\",15.4,,,,,,,PM6:DTTC-4Cl,,,,,,,,,,,,1.5,,,,74.1,22.6,,,,,,,920\r\n\"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\",13.3,,,,,,,PM6:SeTlC4Cl-DIO,,,,,,,,,,,,1.51,,,,75,22.9,,,,,,,780\r\n\"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\",10.4,,,,,,,PBDB-T:IDT-EDOT:PC71BM,,,,,,,,,,,,1.52,,,,68,18,,,,,,,850\r\n\"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\",10.7,,,,,,,PM6:SeTlC4Cl,,,,,,,,,,,,1.53,,,,56.7,22.2,,,,,,,850\r\n\"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\",13.6,,,,,,,BTR:NITI:PC71BM,,,,,,,,,,,,1.54,,,,73.8,19.5,,,,,,,940\r\n\"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\",12,,,,,,,PM6:IT-4F,,,,,,,,,,,,1.55,,,,73.3,19.5,,,,,,,840\r\n\"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\",12.1,,,,,,,PBDB-T-2F:IT-4F,,,,,,,,,,,,1.56,,,,70.1,20.9,,,,,,,826\r\n\"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\",13.9,,,,,,,PM6:DTTC-4F,,,,,,,,,,,,1.58,,,,67.4,21.7,,,,,,,950\r\n\"Y. Lin, B. Adilbekova, Y. Firdaus, E. Yengel, H. Faber, M. Sajjad, X. Zheng, E. Yarali, A. Seitkhan, O. M. Bakr, A. El-Labban, U. Schwingenschlögl, V. Tung, I. McCulloch, F. Laquai, T. D. Anthopoulos, Adv. Mater. 2019, 31, 1902965.\",13.5,,,,,,,PBDB-T-SF:IT-4F,,,,,,,,,,,,1.58,,,,74.53,20.6,,,,,,,880\r\n\"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\",13.4,,,,,,,PM6:DTC-4F,,,,,,,,,,,,1.61,,,,70.5,20.2,,,,,,,940\r\n\"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\",12.1,,,,,,,PBDB-T-2Cl:MF1,,,,,,,,,,,,1.61,,,,73,18.1,,,,,,,916\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\",11,,,,,,, ,,,,,,,,,,,,1.62,,,,71.5,19.4,,,,,,,793\r\n\"Z. Luo, C. Sun, S. Chen, Z.-G. Zhang, K. Wu, B. Qiu, C. Yang, Y. Li, C. Yang, Adv. Energy Mater. 2018, 8, 1800856.\",12.2,,,,,,,PTQ10:IDTPC,,,,,,,,,,,,1.62,,,,75,17.5,,,,,,,930\r\n\"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\",12.8,,,,,,,PTQ10:IDIC-2F,,,,,,,,,,,,1.63,,,,73.6,19.1,,,,,,,910\r\n\"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\",12.9,,,,,,,PTQ10:IDIC,,,,,,,,,,,,1.64,,,,71.3,17.4,,,,,,,960\r\n\"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\",9.3,,,,,,,J51:ITIC,,,,,,,,,,,,1.65,,,,68.7,16.5,,,,,,,820\r\n\"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\",12.1,,,,,,, ,,,,,,,,,,,,1.66,,,,73.2,20.3,,,,,,,815\r\n\"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\",10.2,,,,,,,P4TIF:PC61BM,,,,,,,,,,,,1.67,,,,59.9,21,,,,,,,810\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2016, 24, 3.\",11.5,,,,,,, ,,,,,,,,,,,,1.67,,,,73.7,19.7,,,,,,,791\r\n\"D. Baran, N. Gasparini, A. Wadsworth, C. H. Tan, N. Wehbe, X. Song, Z. Hamid, W. Zhang, M. Neophytou, T. Kirchartz, C. J. Brabec, J. R. Durrant, I. McCulloch, Nat. Commun. 2018, 9, 2059.\",12,,,,,,,PBDTTT-EFT:EHIDTBR,,,,,,,,,,,,1.68,,,,63,18.5,,,,,,,1030\r\n\"C. Li, J. Song, Y. Cai, G. Han, W. Zheng, Y. Yi, H. S. Ryu, H. Y. Woo, Y. Sun, J. Energy Chem. 2020, 40, 144.\",8.9,,,,,,,PBT1-C:NFA,,,,,,,,,,,,1.69,,,,72.9,13.9,,,,,,,878\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\",11.1,,,,,,, ,,,,,,,,,,,,1.7,,,,71.9,17.8,,,,,,,867\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\",10,,,,,,, ,,,,,,,,,,,,1.72,,,,66.4,16.8,,,,,,,899\r\n\"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\",7.5,,,,,,,BDT-ffBX-DT:PDI4,,,,,,,,,,,,1.79,,,,62.1,10.6,,,,,,,1140\r\n\"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\",6.2,,,,,,,BDT-ffBX-DT:SFPDI,,,,,,,,,,,,1.79,,,,56.6,8.9,,,,,,,1230\r\n\"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\",9,,,,,,,BTR:PC71BM,,,,,,,,,,,,1.85,,,,72.9,13.8,,,,,,,900\r\n\"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\",7.6,,,,,,,PBDB-T:PC71BM,,,,,,,,,,,,1.85,,,,69.1,13.3,,,,,,,830\r\n\"M. Li, H. Wang, Y. Liu, Y. Zhou, H. Lu, J. Song, Z. Bo, Dyes Pigm. 2020, 175, 108186.\",7.4,,,,,,,PBDB-T:NDP-Se-DIO,,,,,,,,,,,,1.86,,,,61.9,12.7,,,,,,,940\r\n\"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\",5.7,,,,,,,PBDB-T-2Cl:PC61BM,,,,,,,,,,,,1.88,,,,55.9,10.7,,,,,,,950\r\n\"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\",3.7,,,,,,,P3HT:PCBM,,,,,,,,,,,,2.01,,,,59.2,10.4,,,,,,,592\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\",11,,,,,,,,,,,,,,,, ,,,1.44,,,,70.3,21.9,,,,,,,714\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\",11.4,,,,,,,,,,,,,,,, ,,,1.52,,,,71.9,21.3,,,,,,,743\r\n\"T.-K. Chang, Y. Chi, RSC Adv. 2017, 7, 42013.\",10.1,,,,,,,,,,,,,,,,TF-tBu_C3F7,,,1.59,,,,76.9,18.5,,,,,,,710\r\n\"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\",7.8,,,,,,,,,,,,,,,,YD2,,,1.74,,,,72.7,15.4,,,,,,,694\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",10,,,,,,,,,,,,,,,,N719,,,1.77,,,,74.7,18.1,,,,,,,740\r\n\"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\",6.5,,,,,,,,,,,,,,,,SK7,,,1.8,,,,74.5,13.3,,,,,,,663\r\n\"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\",6.4,,,,,,,,,,,,,,,,AN-11,,,1.82,,,,71.8,13.1,,,,,,,680\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\",12.3,,,,,,,,,,,,,,,, ,,,1.85,,,,79.1,15.2,,,,,,,1020\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",8.3,,,,,,,,,,,,,,,,N719,,,1.86,,,,71.7,14.8,,,,,,,782\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321\",9.1,,,,,,,,,,,,,,,,L351,,,1.87,,,,76.7,11.2,,,,,,,1060\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",7.8,,,,,,,,,,,,,,,,TY4,,,1.88,,,,74.7,14.3,,,,,,,730\r\n\"X. Wang, A. Bolag, W. Yun, Y. Du, C. Eerdun, X. Zhang, T. Bao, J. Ning, H. Alata, T. Ojiyed, J. Mol. Struct. 2020, 1206, 127694.\",8.5,,,,,,,,,,,,,,,,N719+W2,,,1.89,,,,68.8,21.3,,,,,,,580\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321\",11.2,,,,,,,,,,,,,,,,L350,,,1.93,,,,75.6,13,,,,,,,1140\r\n\"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\",3,,,,,,,,,,,,,,,,AN-14,,,1.97,,,,79.4,6.3,,,,,,,600\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",5.4,,,,,,,,,,,,,,,,SK6,,,1.99,,,,69.5,11.3,,,,,,,689\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",6.3,,,,,,,,,,,,,,,,CW10+SK6,,,2,,,,71.7,12,,,,,,,732\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321\",9.2,,,,,,,,,,,,,,,,L349,,,2.01,,,,72.1,11,,,,,,,1160\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",8.1,,,,,,,,,,,,,,,,TY6,,,2.02,,,,75,14.3,,,,,,,760\r\n\"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\",3.9,,,,,,,,,,,,,,,,AN-12,,,2.05,,,,77.5,7.4,,,,,,,680\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",6.9,,,,,,,,,,,,,,,,TY3,,,2.09,,,,76.3,11.6,,,,,,,780\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",5.8,,,,,,,,,,,,,,,,CW10,,,2.12,,,,72.7,10.8,,,,,,,739\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",5.8,,,,,,,,,,,,,,,,MS3,,,2.23,,,,74.8,10.2,,,,,,,760\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321\",5.3,,,,,,,,,,,,,,,,L348,,,2.32,,,,70.8,6.4,,,,,,,1170\r\n\"T. K. Todorov, J. Tang, S. Bag, O. Gunawan, T. Gokmen, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2013, 3, 34.\",10.8,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.09,,,,62.6,38.6,,,,,,,447\r\n\"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcobé, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. Pérez-Rodríguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\",9.4,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.11,,,,63.3,32.5,,,,,,,457\r\n\"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcobé, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. Pérez-Rodríguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\",9.5,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.12,,,,66.4,31.1,,,,,,,460\r\n\"W. Wang, M. T. Winkler, O. Gunawan, T. Gokmen, T. K. Todorov, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2014, 4, 1301465.\",12.6,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.13,,,,69.8,35.2,,,,,,,513\r\n\"T. K. Todorov, J. Tang, S. Bag, O. Gunawan, T. Gokmen, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2013, 3, 34.\",11.1,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.13,,,,69.8,34.5,,,,,,,460\r\n\"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcobé, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. Pérez-Rodríguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\",8.4,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.15,,,,65.7,30,,,,,,,426\r\n\"K. Shen, Y. Zhang, X. Wang, C. Ou, F. Guo, H. Zhu, C. Liu, Y. Gao, R. E. I. Schropp, Z. Li, X. Liu, Y. Mai, Adv. Sci. 2020, 7, 2001013.\",7.5,,,,,,,,,Sb2Se3,,,,,,,,,,1.22,,,,62.4,28.9,,,,,,,413\r\n\"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\",9.2,,,,,,,,,Sb2Se3,,,,,,,,,,1.24,,,,70.6,32.6,,,,,,,400\r\n\"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\",4.8,,,,,,,,,Sb2Se3,,,,,,,,,,1.27,,,,47.3,27.3,,,,,,,370\r\n\"C. Yan, J. Huang, K. Sun, S. Johnston, Y. Zhang, H. Sun, A. Pu, M. He, F. Liu, K. Eder, L. Yang, J. M. Cairney, N. J. Ekins-Daukes, Z. Hameiri, J. A. Stride, S. Chen, M. A. Green, X. Hao, Nat. Energy 2018, 3, 764.\",11,,,,,,,,,Cu2ZnSnS4,,,,,,,,,,1.5,,,,69.3,21.7,,,,,,,731\r\n\"R. Tang, X. Wang, W. Lian, J. Huang, Q. Wei, M. Huang, Y. Yin, C. Jiang, S. Yang, G. Xing, S. Chen, C. Zhu, X. Hao, M. A. Green, T. Chen, Nat. Energy 2020, 5, 587.\",10,,,,,,,,,\"Sb2(S,Se)3\",,,,,,,,,,1.5,,,,63.3,24.1,,,,,,,655\r\n\"K. Timmo, M. Altosaar, M. Pilvet, V. Mikli, M. Grossberg, M. Danilson, T. Raadik, R. Josepson, J. Krustok, M. Kauk-Kuusik, J. Mater. Chem. A 2019, 7, 24281.\",8.73,,,,,,,,,(Cu0.99Ag0.01)1.85(Zn0.8Cd0.2)1.1SnS4,,,,,,,,,,1.52,,,,63.9,20.6,,,,,,,664\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2014, 22, 1.\",19.8,,,,,,,,,CIGS,,,,,,,,,,1.09,,,,79.2,34.9,,,,,,,716\r\n\"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\",21.7,,,,,,,,,CIGS,,,,,,,,,,1.1,,,,74.3,40.7,,,,,,,718\r\n\"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\",26.7,,,,,,,,,Si (crystalline),,,,,,,,,,1.11,,,,84.9,42.7,,,,,,,738\r\n\"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2018, 26, 427.\",22.9,,,,,,,,,CIGS,,,,,,,,,,1.13,,,,79.5,38.8,,,,,,,744\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 805.\",21,,,,,,,,,CIGS,,,,,,,,,,1.14,,,,77.6,35.7,,,,,,,757\r\n\"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\",23.4,,,,,,,,,CIGS,,,,,,,,,,1.15,,,,80.4,39.6,,,,,,,734\r\n\"W. Li, S. Xu, Y. Dai, P. Ma, Y. Feng, W. Li, H. Luo, C. Yang, Mater. Lett. 2019, 244, 43.\",16.3,,,,,,,,,CIGS,,,,,,,,,,1.3,,,,68.1,31.4,,,,,,,762\r\n\"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics Res. Appl. 2019, 27, 3.\",29.1,,,,,,,,,GaAs,,,,,,,,,,1.42,,,,86.7,29.8,,,,,,,1127\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\",21,,,,,,,,,CdTe,,,,,,,,,,1.42,,,,79.4,30.3,,,,,,,1062\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\",18.3,,,,,,,,,CdTe,,,,,,,,,,1.48,,,,77,27,,,,,,,857\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\",10.2,,,,,,,,,Si (amorphous),,,,,,,,,,1.6,,,,69.8,16.4,,,,,,,896\r\n\"T. Matsui, A. Bidiville, K. Maejima, H. Sai, T. Koida, T. Suezaki, M. Matsumoto, K. Saito, I. Yoshida, M. Kondo, Appl. Phys. Lett. 2015, 106, 053901.\",10.6,,,,,,,,,Si (amorphous),,,,,,,,,,1.69,,,,75.6,16.1,,,,,,,896\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, Prog. Photovoltaics 2010, 18, 346.\",10.1,,,,,,,,,Si (amorphous),,,,,,,,,,1.85,,,,67,16.8,,,,,,,886\r\n\"M. Ma, Q. Tang, H. Chen, B. He, P. Yang, Sol. Energy Mater. Sol. Cells 2017, 160, 67.\",3.62,,,,,,,,,,(5-AVA)y(MA)1−yPbI3,,,,,,,,,1.47,,,,40.6,14.5,,,,,,,616\r\n\"D. Yang, R. Yang, K. Wang, C. Wu, X. Zhu, J. Feng, X. Ren, G. Fang, S. Priya, S. Liu, Nat. Commun. 2018, 9, 3239.\",18.3,,,,,,,,,,FA0.95Cs0.05PbI3,,,,,,,,,1.54,,,,71.5,23.4,,,,,,,1090\r\n\"J. H. Heo, D. H. Shin, D. H. Song, D. H. Kim, S. J. Lee, S. H. Im, J. Mater. Chem. A 2018, 6, 8251.\",18.2,,,,,,,,,,FAPbI3 xBrx,,,,,,,,,1.54,,,,76.9,22.1,,,,,,,1070\r\n\"C. Wang, L. Guan, D. Zhao, Y. Yu, C. R. Grice, Z. Song, R. A. Awni, J. Chen, J. Wang, X. Zhao, Y. Yan, ACS Energy Lett. 2017, 2, 2118.\",17.1,,,,,,,,,,MA0.7FA0.3PbI3,,,,,,,,,1.56,,,,75.4,22.1,,,,,,,1101\r\n\"K. Huang, Y. Peng, Y. Gao, J. Shi, H. Li, X. Mo, H. Huang, Y. Gao, L. Ding, J. Yang, Adv. Energy Mater. 2019, 9, 1901419.\",19.5,,,,,,,,,,FA0.945MA0.025Cs0.03Pb(I0.975Br0.025)3,,,,,,,,,1.57,,,,76,23.1,,,,,,,1110\r\n\"X. Dai, Y. Deng, C. H. Van Brackle, S. Chen, P. N. Rudd, X. Xiao, Y. Lin, B. Chen, J. Huang, Adv. Energy Mater. 2020, 10, 1903108.\",19.3,,,,,,,,,,MAPbI3 NH4Cl,,,,,,,,,1.59,,,,78.1,22.7,,,,,,,1090\r\n\"Z. Wang, L. Zeng, C. Zhang, Y. Lu, S. Qiu, C. Wang, C. Liu, L. Pan, S. Wu, J. Hu, G. Liang, P. Fan, H.-J. Egelhaaf, C. J. Brabec, F. Guo, Y. Mai, Adv. Funct. Mater. 2020, 30, 2001240.\",19,,,,,,,,,,MAPbI3,,,,,,,,,1.6,,,,80,21.8,,,,,,,1090\r\n\"J. Feng, X. Zhu, Z. Yang, X. Zhang, J. Niu, Z. Wang, S. Zuo, S. Priya, S. Liu, D. Yang, Adv. Mater. 2018, 30, 1801418.\",18.4,,,,,,,,,,MAPbI3 dimethylsulfide,,,,,,,,,1.6,,,,74.2,22.5,,,,,,,1103\r\n\"C. Liu, L. Zhang, X. Zhou, J. Gao, W. Chen, X. Wang, B. Xu, Adv. Funct. Mater. 2019, 29, 1807604.\",17.3,,,,,,,,,,Cs0.05FA0.81MA0.14PbI2.55Br0.45,,,,,,,,,1.61,,,,74.9,21.7,,,,,,,1062\r\n\"B. Cao, L. Yang, S. Jiang, H. Lin, N. Wang, X. Li, J. Mater. Chem. A 2019, 7, 4960.\",19.1,,,,,,,,,,Rb0.01K0.04 (Cs0.05(FA0.83MA0.17)0.95)0.95(I0.83Br0.17)3,,,,,,,,,1.61,,,,79.2,21.2,,,,,,,1135\r\n\"D. Xin, S. Tie, X. Zheng, J. Zhu, W.-H. Zhang, J. Energy Chem. 2020, 46, 173.\",18,,,,,,,,,,Cs0.06FA0.79MA0.15PbI2.55Br0.45,,,,,,,,,1.62,,,,72.1,22.3,,,,,,,1120\r\n\"M. Gao, X. Han, X. Zhan, P. Liu, Y. Shan, Y. Chen, J. Li, R. Zhang, S. Wang, Q. Zhang, Y. Zheng, L. Chen, Mater. Lett. 2019, 248, 16.\",10.4,,,,,,,,,,(FAPbI3)0.85(MAPbBr3)0.15,,,,,,,,,1.63,,,,52.8,19.2,,,,,,,1030\r\n\"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\",11.2,,,,,,,,,,MAPbI3,,,,,,,,,1.65,,,,64.9,18.4,,,,,,,940\r\n\"J. Xi, Z. Wu, K. Xi, H. Dong, B. Xia, T. Lei, F. Yuan, W. Wu, B. Jiao, X. Hou, Nano Energy 2016, 26, 438.\",7.9,,,,,,,,,,(α-FAPbI3)0.5(MAPbI2Br)0.5,,,,,,,,,1.65,,,,70.7,10.8,,,,,,,1090\r\n\"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\",10.6,,,,,,,PTB7-Th:IEICO-4F,,,,,,,,,,,,1.32,,,,63.2,24.3,,,,,,,690\r\n\"W. Zhang, W. Song, J. Huang, L. Huang, T. Yan, J. Ge, R. Peng, Z. Ge, J. Mater. Chem. A 2019, 7, 22021.\",13.4,,,,,,,PM6:Y6,,,,,,,,,,,,1.39,,,,70,23,,,,,,,829\r\n\"X. Chen, G. Xu, G. Zeng, H. Gu, H. Chen, H. Xu, H. Yao, Y. Li, J. Hou, Y. Li, Adv. Mater. 2020, 32, 1908478.\",15.2,,,,,,,PBDB-T-2F:Y6,,,,,,,,,,,,1.4,,,,73,25.1,,,,,,,832\r\n\"T. Yan, W. Song, J. Huang, R. Peng, L. Huang, Z. Ge, Adv. Mater. 2019, 31, 1902210.\",14.1,,,,,,,PM6:Y6:PC71BM,,,,,,,,,,,,1.4,,,,72,23.6,,,,,,,828\r\n\"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\",12,,,,,,,PM6:IT-4F,,,,,,,,,,,,1.55,,,,73.3,19.5,,,,,,,840\r\n\"X. Dong, P. Shi, L. Sun, J. Li, F. Qin, S. Xiong, T. Liu, X. Jiang, Y. Zhou, J. Mater. Chem. A 2019, 7, 1989.\",11.6,,,,,,,PBDB-T-2F:IT-4F,,,,,,,,,,,,1.56,,,,72.2,19.6,,,,,,,820\r\n\"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\",12.1,,,,,,,PBDB-T-2F:IT-4F,,,,,,,,,,,,1.56,,,,70.1,20.9,,,,,,,826\r\n\"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\",10.9,,,,,,,PBDB-T:ITIC,,,,,,,,,,,,1.61,,,,64.8,18.7,,,,,,,900\r\n\"Y. Yang, J. Ou, X. Lv, C. Meng, Y. Mai, Sol. Energy 2019, 180, 57.\",9.2,,,,,,,PTB7-Th:PC71BM,,,,,,,,,,,,1.63,,,,74.7,16,,,,,,,770\r\n\"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\",9.3,,,,,,,J51:ITIC,,,,,,,,,,,,1.65,,,,68.7,16.5,,,,,,,820\r\n\"T. Xu, C. Gong, S. Wang, H. Lian, W. Lan, G. Lévêque, B. Grandidier, J. Plain, R. Bachelot, B. Wei, F. Zhu, Sol. RRL 2020, 4, 1900522.\",8.2,,,,,,,PBDB-T:ITIC,,,,,,,,,,,,1.65,,,,68.6,13.4,,,,,,,890\r\n\"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\",3.7,,,,,,,P3HT:PCBM,,,,,,,,,,,,2.01,,,,59.2,10.4,,,,,,,592\r\n\"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\",4.6,,,,,,,,,,,,,,,,N719,,,1.74,,,,58,10.5,,,,,,,750\r\n\"T. Yamaguchi, N. Tobe, D. Matsumoto, T. Nagai, H. Arakawa, Sol. Energy Mater. Sol. Cells 2010, 94, 812.\",7.6,,,,,,,,,,,,,,,,N719,,,1.75,,,,69.2,15,,,,,,,732\r\n\"Y. Wang, P. Cheng, C. Feng, H. Zhang, W. Zhao, Sol. Energy 2019, 180, 423.\",6.5,,,,,,,,,,,,,,,,N719,,,1.79,,,,68,13.19,,,,,,,729\r\n\"H. Lee, J. Kim, D. Y. Kim, Y. Seo, Org. Electron. 2018, 52, 103.\",6.3,,,,,,,,,,,,,,,,(JH-1)0.6(SQ2)0.4,,,1.81,,,,67.9,12.3,,,,,,,754\r\n\"Y. Xiao, J. Wu, G. Yue, J. Lin, M. Huang, Z. Lan, Electrochim. Acta 2011, 56, 8545.\",6,,,,,,,,,,,,,,,,N719,,,1.88,,,,71,11.2,,,,,,,750\r\n\"L. Song, Y. Guan, P. Du, Y. Yang, F. Ko, J. Xiong, Sol. Energy Mater. Sol. Cells 2016, 147, 134.\",4.2,,,,,,,,,,,,,,,,N719,,,1.94,,,,57.2,10.3,,,,,,,710\r\n\"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\",6.4,,,,,,,,,,,,,,,,N719,,,1.99,,,,53.4,18.1,,,,,,,660\r\n\"Q. Tang, H. Shen, H. Yao, K. Gao, Y. Jiang, Y. Li, Y. Liu, L. Zhang, Z. Ni, Q. Wei, Renewable Energy 2019, 133, 883.\",17,,,,,,,,,c-Si,,,,,,,,,,1.14,,,,70.8,36.6,,,,,,,656\r\n\"A. Chirilă, P. Reinhard, F. Pianezzi, P. Bloesch, A. R. Uhl, C. Fella, L. Kranz, D. Keller, C. Gretener, H. Hagendorfer, D. Jaeger, R. Erni, S. Nishiwaki, S. Buecheler, A. N. Tiwari, Nat. Mater. 2013, 12, 1107.\",20.4,,,,,,,,,CIGS,,,,,,,,,,1.2,,,,78.9,35.1,,,,,,,736\r\n\"R. Kaczynski, J. Lee, J. V. Alsburg, B. Sang, U. Schoop, J. Britt, presented at 2017 IEEE 44th Photovoltaic Specialist Conf. (PVSC), June 2017.\",18.7,,,,,,,,,CIGS,,,,,,,,,,1.22,,,,74.4,35,,,,,,,720\r\n\"K. Ruan, K. Ding, Y. Wang, S. Diao, Z. Shao, X. Zhang, J. Jie, J. Mater. Chem. A 2015, 3, 14370.\",8.4,,,,,,,,,c-Si,,,,,,,,,,1.32,,,,63,24.3,,,,,,,550\r\n\"S. Moon, K. Kim, Y. Kim, J. Heo, J. Lee, Sci. Rep. 2016, 6, 30107.\",22.1,,,,,,,,,GaAs,,,,,,,,,,1.42,,,,83.4,27.1,,,,,,,980\r\n\"H. P. Mahabaduge, W. L. Rance, J. M. Burst, M. O. Reese, D. M. Meysing, C. A. Wolden, J. Li, J. D. Beach, T. A. Gessert, W. K. Metzger, S. Garner, T. M. Barnes, Appl. Phys. Lett. 2015, 106, 133501.\",16.4,,,,,,,,,CdTe,,,,,,,,,,1.46,,,,77.4,25.5,,,,,,,831\r\n\"L. Kranz, C. Gretener, J. Perrenoud, R. Schmitt, F. Pianezzi, F. La Mattina, P. Blösch, E. Cheah, A. Chirilă, C. M. Fella, H. Hagendorfer, T. Jäger, S. Nishiwaki, A. R. Uhl, S. Buecheler, A. N. Tiwari, Nat. Commun. 2013, 4, 2306.\",11.5,,,,,,,,,CdTe,,,,,,,,,,1.49,,,,63.9,22,,,,,,,821\r\n\"T. Söderström, F.-J. Haug, V. Terrazzoni-Daudrix, C. Ballif, J. Appl. Phys. 2008, 103, 114509.\",8.8,,,,,,,,,a-Si:H,,,,,,,,,,1.79,,,,70,14.3,,,,,,,888\r\n\"C. Zhang, Y. Song, M. Wang, M. Yin, X. Zhu, L. Tian, H. Wang, X. Chen, Z. Fan, L. Lu, D. Li, Adv. Funct. Mater. 2017, 27, 1604720.\",8.2,,,,,,,,,a-Si:H,,,,,,,,,,1.88,,,,64,15.6,,,,,,,820\r\n\"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\",12.2,,,,,3,MAPbI3,,,,,,,,,,,,,1.53,,,,68.5,17.5,,,,,,,1017\r\n\"B. Chen, Y. Bai, Z. Yu, T. Li, X. Zheng, Q. Dong, L. Shen, M. Boccard, A. Gruverman, Z. Holman, J. Huang, Adv. Energy Mater. 2016, 6, 1601128.\",16.5,,,,,5,MAPbI3,,,,,,,,,,,,,1.6,,,,74.2,20.6,,,,,,,1080\r\n\"P. You, Z. Liu, Q. Tai, S. Liu, F. Yan, Adv. Mater. 2015, 27, 3632.\",12,,,,,5,MAPbI3−xClx,,,,,,,,,,,,,1.61,,,,65.3,19.2,,,,,,,960\r\n\"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\",11.2,,,,,5,MAPbI3,,,,,,,,,,,,,1.65,,,,64.9,18.4,,,,,,,940\r\n\"J. H. Heo, H. J. Han, M. Lee, M. Song, D. H. Kim, S. H. Im, Energy Environ. Sci. 2015, 8, 2922.\",15.8,,,,,6,MAPbI3,,,,,,,,,,,,,1.6,,,,74.4,19.3,,,,,,,1100\r\n\"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\",13.6,,,,,7,MAPbI3,,,,,,,,,,,,,1.55,,,,67.5,20.4,,,,,,,988\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",17.5,,,,,10,MAPbI3,,,,,,,,,,,,,1.59,,,,73.1,22.4,,,,,,,1070\r\n\"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\",16.1,,,,,10,Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.65,,,,74.5,20.4,,,,,,,1060\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",13.2,,,,,12,MAPbI3,,,,,,,,,,,,,1.6,,,,67.8,19.5,,,,,,,1000\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",14.9,,,,,13,MAPbI2.5Br0.5,,,,,,,,,,,,,1.67,,,,68.4,19.8,,,,,,,1100\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",13,,,,,14,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,69.9,19.1,,,,,,,970\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",11.9,,,,,15,MAPbI3,,,,,,,,,,,,,1.61,,,,66.3,17.8,,,,,,,1000\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",13.7,,,,,16,MAPbI2Br,,,,,,,,,,,,,1.76,,,,73.4,16.7,,,,,,,1120\r\n\"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\",12.8,,,,,17,Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.65,,,,74.1,16.6,,,,,,,1040\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",12.2,,,,,18,MAPbI2Br,,,,,,,,,,,,,1.77,,,,72.7,15.1,,,,,,,1110\r\n\"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\",9.1,,,,,18,MAPbI3,,,,,,,,,,,,,1.53,,,,61.5,14.6,,,,,,,1017\r\n\"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\",8.8,,,,,19,MAPbI3,,,,,,,,,,,,,1.55,,,,68.3,13.7,,,,,,,941\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",14.7,,,,,20,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.63,,,,75.2,17.6,,,,,,,1108\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",14.2,,,,,21,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.63,,,,73.2,17.4,,,,,,,1117\r\n\"C.-Y. Chang, Y.-C. Chang, W.-K. Huang, K.-T. Lee, A.-C. Cho, C.-C. Hsu, Chem. Mater. 2015, 27, 7119.\",11,,,,,21,MAPbI3,,,,,,,,,,,,,1.63,,,,69.2,15.9,,,,,,,1000\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",13.2,,,,,22,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.61,,,,71.7,17.2,,,,,,,1073\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",12.3,,,,,23,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.61,,,,66.6,17.1,,,,,,,1082\r\n\"S. Xiao, H. Chen, F. Jiang, Y. Bai, Z. Zhu, T. Zhang, X. Zheng, G. Qian, C. Hu, Y. Zhou, Y. Qu, S. Yang, Adv. Mater. Interfaces 2016, 3, 1600484.\",11.3,,,,,23,MAPbI3,,,,,,,,,,,,,1.62,,,,72.3,15.1,,,,,,,1040\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",10.8,,,,,23,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,64.4,17.3,,,,,,,970\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",9.4,,,,,24,MAPbI1.5Br1.5,,,,,,,,,,,,,1.87,,,,61.6,13.6,,,,,,,1120\r\n\"C.-Y. Chang, K.-T. Lee, W.-K. Huang, H.-Y. Siao, Y.-C. Chang, Chem. Mater. 2015, 27, 5122.\",10.8,,,,,25,MAPbI3,,,,,,,,,,,,,1.55,,,,69.7,16.3,,,,,,,950\r\n\"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\",10.2,,,,,26,MAPbI3,,,,,,,,,,,,,1.63,,,,78.1,12.2,,,,,,,1070\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",12.1,,,,,27,MAPbI3,,,,,,,,,,,,,1.6,,,,66.2,18.3,,,,,,,1000\r\n\"F. Guo, H. Azimi, Y. Hou, T. Przybilla, M. Hu, C. Bronnbauer, S. Langner, E. Spiecker, K. Forberich, C. J. Brabec, Nanoscale 2015, 7, 1642.\",8.5,,,,,28,MAPbI3−xClx,,,,,,,,,,,,,1.6,,,,66.8,13.1,,,,,,,964\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",8.1,,,,,28,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,70.2,11.2,,,,,,,1030\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",12.8,,,,,30,MAPbI3−xClx,,,,,,,,,,,,,1.62,,,,74.9,16.5,,,,,,,1030\r\n\"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\",7.4,,,,,30,Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.65,,,,62.2,11.8,,,,,,,1010\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",11.9,,,,,31,MAPbI2.5Br0.5,,,,,,,,,,,,,1.69,,,,69.4,16.3,,,,,,,1050\r\n\"C. Roldán-Carmona, O. Malinkiewicz, R. Betancur, G. Longo, C. Momblona, F. Jaramillo, L. Camacho, H. J. Bolink, Energy Environ. Sci. 2014, 7, 2968.\",7.3,,,,,33,MAPbI3,,,,,,,,,,,,,1.55,,,,52.5,13.4,,,,,,,1037\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",11.7,,,,,34,MAPbI3−xClx,,,,,,,,,,,,,1.62,,,,74.6,15.9,,,,,,,990\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",10.3,,,,,36,MAPbI2Br,,,,,,,,,,,,,1.79,,,,65.5,14.6,,,,,,,1080\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",10.8,,,,,37,MAPbI3−xClx,,,,,,,,,,,,,1.62,,,,73.1,14.7,,,,,,,1010\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",7.8,,,,,37,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,69.6,11.6,,,,,,,970\r\n\"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\",10.7,,,,,38,MAPbI3,,,,,,,,,,,,,1.63,,,,77.6,13,,,,,,,1060\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",8.8,,,,,41,MAPbI1.5Br1.5,,,,,,,,,,,,,1.9,,,,62.2,12.8,,,,,,,1110\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",10.3,,,,,42,MAPbI3−xClx,,,,,,,,,,,,,1.42,,,,75.6,13.6,,,,,,,1000\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",8.5,,,,,45,MAPbI3−xClx,,,,,,,,,,,,,1.64,,,,73.5,12.6,,,,,,,960\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",3.6,,,,,46,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,64.4,5.4,,,,,,,1030\r\n\"S. Bag, M. F. Durstock, Nano Energy 2016, 30, 542.\",4.5,,,,,47,MAPbI3,,,,,,,,,,,,,1.63,,,,63,8.2,,,,,,,880\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.1,,,,,66,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,52.9,2.1,,,,,,,1000\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",7.8,,,,,68,FAPbBr2.43Cl0.57,,,,,,,,,,,,,2.35,,,,72,6.7,,,,,,,1550\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.5,,,,,72,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,74.3,2.1,,,,,,,960\r\n\"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\",0.2,,,,,72,MAPbCl3,,,,,,,,,,,,,3.03,,,,35.4,0.6,,,,,,,1110\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.6,,,,,73,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,73.1,2.2,,,,,,,970\r\n\"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\",0.5,,,,,73,MAPbCl2.4Br0.6,,,,,,,,,,,,,2.84,,,,44.9,0.9,,,,,,,1260\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.5,,,,,74,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,71.1,2.2,,,,,,,970\r\n\"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\",7.6,,,,,2,,,,,,PBDTTT-C-T:PC71BM,,,,,,,,1.66,,,,63.3,15.6,,,,,,,770\r\n\"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\",14.2,,,,,9,,,,,,PM6:Y6,,,,,,,,1.42,,,,72.3,23,,,,,,,854\r\n\"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\",7.1,,,,,11,,,,,,PBDTTT-C-T:PC71BM,,,,,,,,1.66,,,,64.4,14.5,,,,,,,760\r\n\"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\",13.3,,,,,13,,,,,,PM6:Y6,,,,,,,,1.42,,,,71.9,21.7,,,,,,,853\r\n\"T. Xiao, J. Wang, S. Yang, Y. Zhu, D. Li, Z. Wang, S. Feng, L. Bu, X. Zhan, G. Lu, J. Mater. Chem. A 2020, 8, 401.\",11.1,,,,,14,,,,,,PTB7-Th:FNIC2,,,,,,,,1.45,,,,71.3,21.4,,,,,,,727\r\n\"T. Xiao, J. Wang, S. Yang, Y. Zhu, D. Li, Z. Wang, S. Feng, L. Bu, X. Zhan, G. Lu, J. Mater. Chem. A 2020, 8, 401.\",8.9,,,,,15,,,,,,PTB7-Th:FNIC1,,,,,,,,1.52,,,,63,18.3,,,,,,,772\r\n\"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\",12.6,,,,,17,,,,,,PBDB-T-2F:Y6,,,,,,,,1.39,,,,73.2,21.2,,,,,,,810\r\n\"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\",11.7,,,,,18,,,,,,PBDB-T-2F:Y6,,,,,,,,1.39,,,,69.6,20.7,,,,,,,810\r\n\"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\",12.4,,,,,19,,,,,,PM6:Y6,,,,,,,,1.42,,,,71.4,20.4,,,,,,,852\r\n\"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\",10.5,,,,,21,,,,,,PBDB-T-2F:Y6,,,,,,,,1.39,,,,68.3,19.3,,,,,,,800\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\",11,,,,,25,,,,,,PCE-10:A078,,,,,,,,1.34,,,,70,20.9,,,,,,,750\r\n\"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\",10.2,,,,,25,,,,,,PTB7-Th:FOIC,,,,,,,,1.4,,,,68.3,20.3,,,,,,,736\r\n\"Y. Bai, C. Zhao, X. Chen, S. Zhang, S. Zhang, T. Hayat, A. Alsaedi, Z. a. Tan, J. Hou, Y. Li, J. Mater. Chem. A 2019, 7, 15887.\",12.9,,,,,26,,,,,,PBDB-T-2F:Y6,,,,,,,,1.4,,,,72.4,21.6,,,,,,,825\r\n\"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\",5.6,,,,,28,,,,,,PBDTTT-C-T:PC71BM,,,,,,,,1.66,,,,61.9,11.9,,,,,,,760\r\n\"R. Xia, C. J. Brabec, H.-L. Yip, Y. Cao, Joule 2019, 3, 2241.\",10.8,,,,,30,,,,,,PTB7-Th:IEICO-4F,,,,,,,,1.35,,,,68.7,21.9,,,,,,,718\r\n\"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\",9.1,,,,,34,,,,,,PTB7-Th:FOIC,,,,,,,,1.4,,,,67.1,18.5,,,,,,,733\r\n\"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\",8.8,,,,,36,,,,,,PCE-10:BT-CIC:TT-FIC,,,,,,,,1.37,,,,71.9,18,,,,,,,680\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",6.9,,,,,36,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,66.5,11.6,,,,,,,890\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",6.1,,,,,37,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,66.8,10.2,,,,,,,890\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",4.9,,,,,39,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,67.9,8.3,,,,,,,880\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\",8.1,,,,,43,,,,,,PCE-10:A078,,,,,,,,1.34,,,,68.1,16.3,,,,,,,730\r\n\"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\",8,,,,,44,,,,,,PCE-10:BT-CIC:TT-FIC,,,,,,,,1.37,,,,72.6,16.2,,,,,,,680\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\",10.8,,,,,46,,,,,,PCE-10:A078,,,,,,,,1.34,,,,70.6,20.4,,,,,,,750\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\",7.1,,,,,47,,,,,,PCE-10:A078,,,,,,,,1.34,,,,68,14.3,,,,,,,730\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",2.4,,,,,47,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,68.2,4.1,,,,,,,860\r\n\"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\",7.2,,,,,49,,,,,,PCE-10:BT-CIC:TT-FIC,,,,,,,,1.37,,,,72.6,14.8,,,,,,,670\r\n\"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\",8.3,,,,,50,,,,,,PTB7-Th:FOIC:PC71BM,,,,,,,,1.38,,,,66.8,16.7,,,,,,,746\r\n\"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\",7.4,,,,,51,,,,,,PTB7:FOIC:PC71BM,,,,,,,,1.39,,,,66.7,14.7,,,,,,,749\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",1.8,,,,,53,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,54.8,3.8,,,,,,,890\r\n\"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\",5.7,,,,,53,,,,,,DPP2T:IEICO-4F,,,,,,,,1.32,,,,69.5,10.6,,,,,,,750\r\n\"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\",3.9,,,,,60,,,,,,DPP2T:IEICO-4F,,,,,,,,1.33,,,,70.2,7.34,,,,,,,749\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",5.9,,,,,62,,,,,,PTB7-Th:6TIC-4F,,,,,,,,1.33,,,,66,12.9,,,,,,,690\r\n\"C. Yang, M. Moemeni, M. Bates, W. Sheng, B. Borhan, R. R. Lunt, Adv. Opt. Mater. 2020, 8, 1901536.\",1.2,,,,,73,,,,,,COi8DFIC,,,,,,,,1.5,,,,81,1.54,,,,,,,990\r\n\"Y. Zhao, R. R. Lunt, Adv. Energy Mater. 2013, 3, 1143.\",0.4,,,,,84,,,,,,PBMMA:PEMA:(TBA)2Mo6Cl14,,,,,,,,2.81,,,,65,1.3,,,,,,,520\r\n\"Y. Zhao, G. A. Meek, B. G. Levine, R. R. Lunt, Adv. Opt. Mater. 2014, 2, 606.\",0.4,,,,,86,,,,,,Cy7,,,,,,,,1.52,,,,66,1.2,,,,,,,500\r\n\"C. López-López, S. Colodrero, H. Míguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\",5.2,,,,,1,,,,,,N719,,,,,,,,2,,,,53.7,12.4,,,,,,,780\r\n\"C. López-López, S. Colodrero, H. Míguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\",4.5,,,,,9,,,,,,N719,,,,,,,,2,,,,56,10.3,,,,,,,780\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",4.3,,,,,9,,,,,,N719+SDA,,,,,,,,1.82,,,,60,9.9,,,,,,,720\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",5.2,,,,,10,,,,,,N719,,,,,,,,2.01,,,,57,11.9,,,,,,,770\r\n\"C. López-López, S. Colodrero, H. Míguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\",4.9,,,,,10,,,,,,N719,,,,,,,,2,,,,56.1,11.4,,,,,,,765\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",10.1,,,,,13,,,,,,SGT-021,,,,,,,,1.68,,,,80.2,14.9,,,,,,,851\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",9.9,,,,,14,,,,,,SGT-021,,,,,,,,1.68,,,,78.5,14.9,,,,,,,850\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",9.6,,,,,15,,,,,,SGT-021,,,,,,,,1.68,,,,77.2,14.7,,,,,,,850\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",9.8,,,,,17,,,,,,SGT-021,,,,,,,,1.68,,,,75.5,15.1,,,,,,,855\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",4.2,,,,,23,,,,,,N719+SDA,,,,,,,,1.82,,,,64,9.9,,,,,,,650\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",3.6,,,,,23,,,,,,N719,,,,,,,,2.01,,,,68,8.2,,,,,,,650\r\n\"C. López-López, S. Colodrero, H. Míguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\",3.5,,,,,24,,,,,,N719,,,,,,,,2,,,,60.9,7.3,,,,,,,786\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",2.6,,,,,25,,,,,,N719+SDA,,,,,,,,1.82,,,,71,5.6,,,,,,,650\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",1.5,,,,,30,,,,,,N719,,,,,,,,2.19,,,,70,3.3,,,,,,,640\r\n\"K. Kim, S. K. Nam, J. H. Moon, ACS Appl. Energy Mater. 2020, 3, 5277.\",7.8,,,,,43,,,,,,PdTPBP/BPEA,,,,,,,,1.95,,,,70.8,15.3,,,,,,,720\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",10,,,,,2,,,,CIGS,,,,,,,,,,1.23,,,,66.9,23.3,,,,,,,640\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",9.8,,,,,9,,,,CIGS,,,,,,,,,,1.3,,,,74.1,20.9,,,,,,,630\r\n\"K. Kim, W. N. Shafarman, Nano Energy 2016, 30, 488.\",6.5,,,,,9,,,,CIGS,,,,,,,,,,1.28,,,,46.5,22.9,,,,,,,597\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.5,,,,,16,,,,a-Si:H,,,,,,,,,,1.83,,,,65.3,14.2,,,,,,,810\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.7,,,,,17,,,,a-Si:H,,,,,,,,,,1.83,,,,67.3,14.1,,,,,,,810\r\n\"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\",5.9,,,,,18,,,,a-SiGe:H,,,,,,,,,,2.05,,,,58.3,14.1,,,,,,,720\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.3,,,,,19,,,,a-Si:H,,,,,,,,,,1.87,,,,67.6,13.1,,,,,,,820\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",6.5,,,,,19,,,,CIGS,,,,,,,,,,1.34,,,,63.5,17.5,,,,,,,580\r\n\"S. H. Moon, S. J. Park, Y. J. Hwang, D.-K. Lee, Y. Cho, D.-W. Kim, B. K. Min, Sci. Rep. 2014, 4, 4408.\",1.7,,,,,20,,,,CIGS,,,,,,,,,,1.64,,,,40.8,8.9,,,,,,,495\r\n\"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\",5.5,,,,,22,,,,a-Si:H,,,,,,,,,,2.05,,,,58.6,12.3,,,,,,,760\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",6,,,,,23,,,,a-Si:H,,,,,,,,,,1.92,,,,68.2,10.6,,,,,,,830\r\n\"J. Wook Lim, M. Shin, D. J. Lee, S. Hyun Lee, S. Jin Yun, Sol. Energy Mater. Sol. Cells 2014, 128, 301.\",6.9,,,,,24,,,,a-Si:H,,,,,,,,,,1.68,,,,70.3,10.7,,,,,,,920\r\n\"M. Saifullah, S. Ahn, J. Gwak, S. Ahn, K. Kim, J. Cho, J. H. Park, Y. J. Eo, A. Cho, J.-S. Yoo, J. H. Yun, J. Mater. Chem. A 2016, 4, 10542.\",5.9,,,,,26,,,,CIGS,,,,,,,,,,1.5,,,,57.4,14.6,,,,,,,710\r\n\"A. Mutalikdesai, S. K. Ramasesha, Thin Solid Films 2017, 632, 73.\",0.4,,,,,43,,,,CdTe,,,,,,,,,,1.53,,,,27.2,14.7,,,,,,,101\r\n\"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\",,21.8,22,,21.8,,Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3,,,,,,,,,\"MPP, AM1.5G, N2, 40 °C, UV-f\",,4.2,22,1.57,,,,,,,,,,,,\r\n\"D. Bi, X. Li, J. V. Milić, D. J. Kubicki, N. Pellet, J. Luo, T. LaGrange, P. Mettraux, L. Emsley, S. M. Zakeeruddin, M. Grätzel, Nat. Commun. 2018, 9, 4482.\",,20.6,20.2,,20.2,,FAxCs1−xPbI3,,,,,,,,,\"MPP, w-LED, Ar, 55 60 °C\",,4.1,20.1,1.57,,,,,,,,,,,,\r\n\"S. Bai, P. Da, C. Li, Z. Wang, Z. Yuan, F. Fu, M. Kawecki, X. Liu, N. Sakai, J. T.-W. Wang, S. Huettner, S. Buecheler, M. Fahlman, F. Gao, H. J. Snaith, Nature 2019, 571, 245.\",,19.2,19.3,,18.4,,(FA0.83MA0.17)0.95Cs0.05Pb(I0.9Br0.1)3,,,,,,,,,\"OC, AM1.5G, encapsulation, 70 75 °C\",,3.9,19,1.58,,,,,,,,,,,,\r\n\"A. D. Jodlowski, C. Roldán-Carmona, G. Grancini, M. Salado, M. Ralaiarisoa, S. Ahmad, N. Koch, L. Camacho, G. de Miguel, M. K. Nazeeruddin, Nat. Energy 2017, 2, 972.\",,17.1,11.6,,9.5,,MA0.85Gua0.15PbI3,,,,,,,,,\"MPP, AM1.5G, Ar, 60 °C\",,2.8,11.1,1.59,,,,,,,,,,,,\r\n\"L. Wang, H. Zhou, J. Hu, B. Huang, M. Sun, B. Dong, G. Zheng, Y. Huang, Y. Chen, L. Li, Z. Xu, N. Li, Z. Liu, Q. Chen, L.-D. Sun, C.-H. Yan, Science 2019, 363, 265.\",,19.2,19.5,,17.6,,MAPbI3−xClx,,,,,,,,,\"OC, AM1.5G\",,4.1,19.1,1.6,,,,,,,,,,,,\r\n\"S. Yang, S. Chen, E. Mosconi, Y. Fang, X. Xiao, C. Wang, Y. Zhou, Z. Yu, J. Zhao, Y. Gao, F. De Angelis, J. Huang, Science 2019, 365, 473.\",,19.6,19.6,,18.8,,Cs0.05FA0.81MA0.14PbI2.55Br0.45,,,,,,,,,\"MPP-RL, AM1.5G, encapsulation, 50 70% RH, 65 °C\",,3.9,19.4,1.6,,,,,,,,,,,,\r\n\"A. D. Jodlowski, C. Roldán-Carmona, G. Grancini, M. Salado, M. Ralaiarisoa, S. Ahmad, N. Koch, L. Camacho, G. de Miguel, M. K. Nazeeruddin, Nat. Energy 2017, 2, 972.\",,18.1,11.9,,13.6,,MA0.75Gua0.25PbI3,,,,,,,,,\"MPP, AM1.5G, Ar, 60 °C\",,2.6,13,1.61,,,,,,,,,,,,\r\n\"J. A. Christians, P. Schulz, J. S. Tinkham, T. H. Schloemer, S. P. Harvey, B. J. Tremolet de Villers, A. Sellinger, J. J. Berry, J. M. Luther, Nat. Energy 2018, 3, 68.\",,12.2,13.3,,12.3,,(FA0.79MA0.16Cs0.05)0.97Pb(I0.84Br0.16)2.97,,,,,,,,,\"77 mW cm−2, MPP-RL, AM1.5G, RH<25%, 26 °C\",,2.1,9.9,1.63,,,,,,,,,,,,\r\n\"M. Saliba, T. Matsui, J.-Y. Seo, K. Domanski, J.-P. Correa-Baena, M. K. Nazeeruddin, S. M. Zakeeruddin, W. Tress, A. Abate, A. Hagfeldt, M. Grätzel, Energy Environ. Sci. 2016, 9, 1989.\",,20.1,17.8,, ,,Cs0.1(MA0.17FA0.83)0.9Pb(I0.83Br0.17)3,,,,,,,,,\"MPP, w-LED, N2, 25 °C\",,3.7, ,1.64,,,,,,,,,,,,\r\n\"K. Domanski, E. A. Alharbi, A. Hagfeldt, M. Grätzel, W. Tress, Nat. Energy 2018, 3, 61.\",,19.7,17.2,, ,,Cs0.5(FA0.83MA0.17)0.95Pb(I0.83Br0.17)3,,,,,,,,,\"MPP, w-LED, N2, 20 °C\",,3.5, ,1.64,,,,,,,,,,,,\r\n\"K. A. Bush, A. F. Palmstrom, Z. J. Yu, M. Boccard, R. Cheacharoen, J. P. Mailoa, D. P. McMeekin, R. L. Z. Hoye, C. D. Bailie, T. Leijtens, I. M. Peters, M. C. Minichetti, N. Rolston, R. Prasanna, S. Sofia, D. Harwood, W. Ma, F. Moghadam, H. J. Snaith, T. Buonassisi, Z. C. Holman, S. F. Bent, M. D. McGehee, Nat. Energy 2017, 2, 17009.\",,13,14.7,,13,,Cs0.17FA0.83Pb(Br0.17I0.83)3,,,,,,,,,\"MPP, AM1.5G, 40% RH, 35 °C\",,2.8,14.1,1.66,,,,,,,,,,,,\r\n\"M. Chen, M.-G. Ju, H. F. Garces, A. D. Carl, L. K. Ono, Z. Hawash, Y. Zhang, T. Shen, Y. Qi, R. L. Grimm, D. Pacifici, X. C. Zeng, Y. Zhou, N. P. Padture, Nat. Commun. 2019, 10, 16.\",,6.8,6.7,, ,,CsSn0.5Ge0.5I3,,,,,,,,,\"MPP , AM1.5G, N2, 45 °C\",,1.3, ,1.69,,,,,,,,,,,,\r\n\"P. Wang, X. Zhang, Y. Zhou, Q. Jiang, Q. Ye, Z. Chu, X. Li, X. Yang, Z. Yin, J. You, Nat. Commun. 2018, 9, 2225.\",,12.9,13.4,, ,,CsPbI3,,,,,,,,,\"OC, AM1.5G, N2, 25 °C, UV-f\",,2.7, ,1.74,,,,,,,,,,,,\r\n\"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\",,7.8,7.2,,6.8,,,,,,,PBDB-T:ITIC-2F,,,,\"OC, w-LED, N2, 40 °C, UV-f\",,1.5,7,1.56,,,,,,,,,,,,\r\n\"C. Xie, T. Heumüller, W. Gruber, X. Tang, A. Classen, I. Schuldes, M. Bidwell, A. Späth, R. H. Fink, T. Unruh, I. McCulloch, N. Li, C. J. Brabec, Nat. Commun. 2018, 9, 5335.\",,5,5,,4.7,,,,,,,P3HT:o-IDTBR,,,,\"OC, AM1.5G, N2, UV-f\",,1,4.8,1.57,,,,,,,,,,,,\r\n\"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\",,8,7.4,,7,,,,,,,PBDB-T:ITIC-Th,,,,\"OC, w-LED, N2, 40 °C, UV-f\",,1.5,7.3,1.66,,,,,,,,,,,,\r\n\"A. Classen, T. Heumueller, I. Wabra, J. Gerner, Y. He, L. Einsiedler, N. Li, G. J. Matt, A. Osvet, X. Du, A. Hirsch, C. J. Brabec, Adv. Energy Mater. 2019, 9, 1902124.\",,8.7,8.1,, ,,,,,,,PBDB-T:IDTBR,,,,\"OC, AM1.5G, N2, 35 40 °C\",,1.6, ,1.7,,,,,,,,,,,,\r\n\"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\",,5.9,5.6,,5.4,,,,,,,PBDB-T:PCBM,,,,\"OC, w-LED, N2, 40 °C, UV-f\",,1.1,5.6,1.84,,,,,,,,,,,,\r\n\"M. Raïssi, S. Leroy-Lhez, B. Ratier, Org. Electron. 2016, 37, 183.\",,3.7,3.7,,3.7,,,,,,,P3HT-PCBM,,,,\"OC, AM1.5G, air\",,0.7,3.7,1.94,,,,,,,,,,,,\r\n\"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\",,9,9,,8.2,,,,,,,,,,,\"OC, AM1.5G, 65 °C\",TF-tBu_C3F7,1.8,8.7,1.59,,,,,,,,,,,,\r\n\"S. G. Hashmi, M. Özkan, J. Halme, S. M. Zakeeruddin, J. Paltakari, M. Grätzel, P. D. Lund, Energy Environ. Sci. 2016, 9, 2453.\",,6.5,6.7,,6.3,,,,,,,,,,,\"OC, AM1.5G, 35 °C, UV-f\",N719,1.4,6.6,1.75,,,,,,,,,,,,\r\n\"R. Jiang, A. Anderson, P. R. F. Barnes, L. Xiaoe, C. Law, B. C. O'Regan, J. Mater. Chem. A 2014, 2, 4751.\",,6.3,5.8,,4.8,,,,,,,,,,,\"OC, w-LED, 20 °C\",Z907,1.3,5.5,1.77,,,,,,,,,,,,\r\n\"S. M. Seo, C. K. Kim, H. K. Kim, J. Mater. Chem. A 2019, 7, 14743.\",,9.3,9.9,,7.9,,,,,,,,,,,\"OC, AM1.5G, 50 °C\",N719,1.9,9.2,1.78,,,,,,,,,,,,\r\n\"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\",,8.4,8.3,, ,,,,,,,,,,,\"OC, w-LED\",MK2,1.7, ,1.83,,,,,,,,,,,,\r\n\"J. Xia, Q. Wang, M. Chen, W. Li, J. Liu, J. Chen, H. Wu, S. Fan, Electrochim. Acta 2019, 307, 422.\",,8,8.3,,8.3,,,,,,,,,,,\"OC, AM1.5G\",N719,1.4,8.1,1.85,,,,,,,,,,,,\r\n\"J. Gao, M. Bhagavathi Achari, L. Kloo, Chem. Commun. 2014, 50, 6249.\",,5.8,6.5,,5.9,,,,,,,,,,,\"OC, AM1.5G, 60 °C\",D35,1.3,6.2,2.07,,,,,,,,,,,,\r\n\"T. Jiang, Z. Chen, X. Chen, T. Liu, X. Chen, W. E. I. Sha, H. Zhu, Y. Yang, Sol. RRL 2020, 4, 1900467.\",20.7,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.4,,,,,,,,,1.25,,,,80.2,30.6,,,,,,,843\r\n\"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\",20.4,,,,,,,,,,GuaSCN:(FASnI3)0.6(MAPbI3)0.4,,,,,,,,,1.26,,,,80.2,30.5,,,,,,,834\r\n\"C. Li, Z. Song, D. Zhao, C. Xiao, B. Subedi, N. Shrestha, M. M. Junda, C. Wang, C.-S. Jiang, M. Al-Jassim, R. J. Ellingson, N. J. Podraza, K. Zhu, Y. Yan, Adv. Energy Mater. 2019, 9, 1803135.\",19,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.34(MAPbBr3)0.06,,,,,,,,,1.26,,,,74.5,28.8,,,,,,,888\r\n\"R. Lin, K. Xiao, Z. Qin, Q. Han, C. Zhang, M. Wei, M. I. Saidaminov, Y. Gao, J. Xu, M. Xiao, A. Li, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2019, 4, 864.\",20.9,,,,,,,,,,MA0.3FA0.7Pb0.5Sn0.5I3,,,,,,,,,1.27,,,,80.5,31.4,,,,,,,827\r\n\"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\",20.6,,,,,,,,,,FSA:MA0.3FA0.7Pb0.5Sn0.5I3,,,,,,,,,1.28,,,,80.1,30.6,,,,,,,842\r\n\"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\",21.7,,,,,,,,,,FSA:MA0.3FA0.7Pb0.5Sn0.5I3,,,,,,,,,1.28,,,,80.8,31.6,,,,,,,850\r\n\"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\",20.3,,,,,,,,,,FA0.5MA0.45Cs0.05Pb0.5Sn0.5I3,,,,,,,,,1.28,,,,79.1,30.2,,,,,,,850\r\n\"G. Kapil, T. Bessho, C. H. Ng, K. Hamada, M. Pandey, M. A. Kamarudin, D. Hirotani, T. Kinoshita, T. Minemoto, Q. Shen, T. Toyoda, T. N. Murakami, H. Segawa, S. Hayase, ACS Energy Lett. 2019, 4, 1991.\",18.4,,,,,,,,,,Cs0.025FA0.475MA0.5Sn0.5Pb0.5I3,,,,,,,,,1.28,,,,72,32.8,,,,,,,780\r\n\"S. Shao, Y. Cui, H. Duim, X. Qiu, J. Dong, G. H. ten Brink, G. Portale, R. C. Chiechi, S. Zhang, J. Hou, M. A. Loi, Adv. Mater. 2018, 30, 1803703.\",16,,,,,,,,,,FASn0.5Pb0.5I3,,,,,,,,,1.29,,,,70.8,29.3,,,,,,,771\r\n\"T. S. Ripolles, D. Yamasuso, Y. Zhang, M. A. Kamarudin, C. Ding, D. Hirotani, Q. Shen, S. Hayase, J. Phys. Chem. C 2018, 122, 27284.\",15.9,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.3(MAPbBr3)0.1,,,,,,,,,1.29,,,,78,26.5,,,,,,,770\r\n\"H. Chen, Z. Peng, K. Xu, Q. Wei, D. Yu, C. Han, H. Li, Z. Ning, Sci. China Mater. 2021, 64, 537.\",18.8,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.4,,,,,,,,,1.3,,,,77.3,29.6,,,,,,,820\r\n\"N. Ghimire, R. S. Bobba, A. Gurung, K. M. Reza, M. A. R. Laskar, B. S. Lamsal, K. Emshadi, R. Pathak, M. A. Afroz, A. H. Chowdhury, K. Chen, B. Bahrami, S. I. Rahman, J. Pokharel, A. Baniya, M. T. Rahman, Y. Zhou, Q. Qiao, ACS Appl. Energy Mater. 2021, 4, 1731.\",17.1,,,,,,,,,,FA0.8MA0.15Cs0.05Pb0.5Sn0.5I3,,,,,,,,,1.3,,,,73,27.9,,,,,,,840\r\n\"Y. Wang, J. Tu, T. Li, C. Tao, X. Deng, Z. Li, J. Mater. Chem. A 2019, 7, 7683.\",5,,,,,,,,,,CsSnI3,,,,,,,,,1.31,,,,50.3,23.8,,,,,,,420\r\n\"F. Li, C. Zhang, J.-H. Huang, H. Fan, H. Wang, P. Wang, C. Zhan, C.-M. Liu, X. Li, L.-M. Yang, Y. Song, K.-J. Jiang, Angew. Chem., Int. Ed. 2019, 58, 6688.\",7.1,,,,,,,,,,MASnI3,,,,,,,,,1.31,,,,64,22.9,,,,,,,486\r\n\"G. E. Eperon, T. Leijtens, K. A. Bush, R. Prasanna, T. Green, J. T.-W. Wang, D. P. McMeekin, G. Volonakis, R. L. Milot, R. May, A. Palmstrom, D. J. Slotcavage, R. A. Belisle, J. B. Patel, E. S. Parrott, R. J. Sutton, W. Ma, F. Moghadam, B. Conings, A. Babayigit, H.-G. Boyen, S. Bent, F. Giustino, L. M. Herz, M. B. Johnston, M. D. McGehee, H. J. Snaith, Science 2016, 354, 861.\",14.1,,,,,,,,,,FA0.75Cs0.25Sn0.5Pb0.5I3,,,,,,,,,1.31,,,,71.4,26.7,,,,,,,740\r\n\"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\",11.6,,,,,,,,,,MAPb0.4Sn0.6I2.8Br0.2,,,,,,,,,1.32,,,,68.9,23.4,,,,,,,720\r\n\"T. Ye, K. Wang, Y. Hou, D. Yang, N. Smith, B. Magill, J. Yoon, R. R. H. H. Mudiyanselage, G. A. Khodaparast, K. Wang, S. Priya, J. Am. Chem. Soc. 2021, 143, 4319.\",7.5,,,,,,,,,,CsSnI3:MBAA,,,,,,,,,133,,,,67,24.9,,,,,,,450\r\n\"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. Gödel, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\",10,,,,,,,,,,MAPb0.4Sn0.6I3,,,,,,,,,1.34,,,,63.6,20.5,,,,,,,767\r\n\"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\",12.1,,,,,,,,,,MAPb0.4Sn0.6I2.6Br0.4,,,,,,,,,1.34,,,,75.1,20.7,,,,,,,780\r\n\"X. Lian, J. Chen, Y. Zhang, M. Qin, J. Li, S. Tian, W. Yang, X. Lu, G. Wu, H. Chen, Adv. Funct. Mater. 2019, 29, 1807024.\",16.3,,,,,,,,,,FAPb0.7Sn0.3I3,,,,,,,,,1.35,,,,79,26.5,,,,,,,780\r\n\"B. Li, H. Di, B. Chang, R. Yin, L. Fu, Y.-N. Zhang, L. Yin, Adv. Funct. Mater. 2021, 31, 2007447.\",8.2,,,,,,,,,,CsSnI3,,,,,,,,,1.36,,,,66.1,19.7,,,,,,,630\r\n\"M. Zhang, D. Chi, J. Wang, F. Wu, S. Huang, Sol. Energy 2020, 201, 589.\",14.7,,,,,,,,,,FA0.3MA0.7Pb0.7Sn0.3I3,,,,,,,,,1.37,,,,73.6,27.1,,,,,,,737\r\n\"D. Chi, S. Huang, M. Zhang, S. Mu, Y. Zhao, Y. Chen, J. You, Adv. Funct. Mater. 2018, 28, 1804603.\",17.3,,,,,,,,,,FAPb0.75Sn0.25I3,,,,,,,,,1.38,,,,75.4,28.2,,,,,,,810\r\n\"H. L. Zhu, J. Xiao, J. Mao, H. Zhang, Y. Zhao, W. C. H. Choy, Adv. Funct. Mater. 2017, 27, 1605469.\",15.2,,,,,,,,,,MAPb0.75Sn0.25I3,,,,,,,,,1.38,,,,72.5,26.2,,,,,,,800\r\n\"X. Zhou, L. Zhang, X. Wang, C. Liu, S. Chen, M. Zhang, X. Li, W. Yi, B. Xu, Adv. Mater. 2020, 32, 1908107.\",20.6,,,,,,,,,,FA0.7MA0.3Pb0.7Sn0.3I3,,,,,,,,,1.39,,,,76,26.6,,,,,,,1020\r\n\"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. Gödel, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\",8.2,,,,,,,,,,MAPb0.6Sn0.4I3,,,,,,,,,1.4,,,,61.8,17.8,,,,,,,745\r\n\"P. Wang, F. Li, K.-J. Jiang, Y. Zhang, H. Fan, Y. Zhang, Y. Miao, J.-H. Huang, C. Gao, X. Zhou, F. Wang, L.-M. Yang, C. Zhan, Y. Song, Adv. Sci. 2020, 7, 1903047.\",7.8,,,,,,,,,,MASnI3,,,,,,,,,1.4,,,,66.2,20.7,,,,,,,570\r\n\"D. B. Khadka, Y. Shirai, M. Yanagida, K. Miyano, J. Mater. Chem. C 2020, 8, 2307.\",5.9,,,,,,,,,,FA1−xRbxSnI3,,,,,,,,,1.41,,,,60.6,20,,,,,,,487\r\n\"Z. Yang, A. Rajagopal, C.-C. Chueh, S. B. Jo, B. Liu, T. Zhao, A. K. Y. Jen, Adv. Mater. 2016, 28, 8990.\",14.4,,,,,,,,,,MAPb0.75Sn0.25I3,,,,,,,,,1.42,,,,78,22.4,,,,,,,820\r\n\"K. Nishimura, M. A. Kamarudin, D. Hirotani, K. Hamada, Q. Shen, S. Iikubo, T. Minemoto, K. Yoshino, S. Hayase, Nano Energy 2020, 74, 104858.\",13.2,,,,,,,,,,(FA0.9EA0.1)0.98EDA0.01SnI3,,,,,,,,,1.42,,,,78,20.3,,,,,,,840\r\n\"X. Jiang, F. Wang, Q. Wei, H. Li, Y. Shang, W. Zhou, C. Wang, P. Cheng, Q. Chen, L. Chen, Z. Ning, Nat. Commun. 2020, 11, 1245.\",12.4,,,,,,,,,,PEA0.15FA0.85SnI3:NH4SCN,,,,,,,,,1.43,,,,74.9,17.4,,,,,,,949\r\n\"X. Liu, Y. Wang, T. Wu, X. He, X. Meng, J. Barbaud, H. Chen, H. Segawa, X. Yang, L. Han, Nat. Commun. 2020, 11, 2678.\",10.4,,,,,,,,,,Cs0.2FA0.8SnI3,,,,,,,,,1.44,,,,75.2,21.6,,,,,,,640\r\n\"X. Liu, Y. Wang, T. Wu, X. He, X. Meng, J. Barbaud, H. Chen, H. Segawa, X. Yang, L. Han, Nat. Commun. 2020, 11, 2678.\",10.1,,,,,,,,,,Cs0.2FA0.8SnI3,,,,,,,,,1.44,,,,70.8,22.2,,,,,,,642\r\n\"X. Meng, Y. Wang, J. Lin, X. Liu, X. He, J. Barbaud, T. Wu, T. Noda, X. Yang, L. Han, Joule 2020, 4, 902.\",10.2,,,,,,,,,,FASnI3:FOEI,,,,,,,,,1.44,,,,72.5,22,,,,,,,638\r\n\"S. Ma, X. Gu, A. K. Kyaw, D. H. Wang, S. Priya, T. Ye, ACS Appl. Mater. Interfaces 2021, 13, 1345.\",6,,,,,,,,,,CsSnI3,,,,,,,,,1.48,,,,53.9,23.9,,,,,,,460\r\n\"A. Y. Alsalloum, B. Turedi, K. Almasabi, X. Zheng, R. Naphade, S. D. Stranks, O. F. Mohammed, O. M. Bakr, Energy Environ. Sci. 2021, 14, 2263.\",22.3,,,,,,,,,,FA0.6MA0.4PbI3 (sc),,,,,,,,,1.49,,,,78,26.3,,,,,,,1090\r\n\"Y. Zhao, X. Xu, H. Zhang, J. Shi, L. Zhu, H. Wu, D. Li, Y. Luo, Q. Meng, J. Power Sources 2017, 359, 147.\",19.3,,,,,,,,,,FA0.6MA0.4PbI3,,,,,,,,,1.51,,,,77.5,23.8,,,,,,,1047\r\n\"S. Yuan, Y. Cai, S. Yang, H. Zhao, F. Qian, Y. Han, J. Sun, Z. Liu, S. Liu, Sol. RRL 2019, 3, 1900220.\",22,,,,,,,,,,FA0.85MA0.15PbI3,,,,,,,,,1.52,,,,78.6,24.9,,,,,,,1120\r\n\"J. Jeong, M. Kim, J. Seo, H. Lu, P. Ahlawat, A. Mishra, Y. Yang, M. A. Hope, F. T. Eickemeyer, M. Kim, Y. J. Yoon, I. W. Choi, B. P. Darwich, S. J. Choi, Y. Jo, J. H. Lee, B. Walker, S. M. Zakeeruddin, L. Emsley, U. Rothlisberger, A. Hagfeldt, D. S. Kim, M. Grätzel, J. Y. Kim, Nature 2021, 592, 381.\",25.2,,,,,,,,,,α-FAPbI3,,,,,,,,,1.53,,,,81.8,26.2,,,,,,,1174\r\n\"J. Jeong, M. Kim, J. Seo, H. Lu, P. Ahlawat, A. Mishra, Y. Yang, M. A. Hope, F. T. Eickemeyer, M. Kim, Y. J. Yoon, I. W. Choi, B. P. Darwich, S. J. Choi, Y. Jo, J. H. Lee, B. Walker, S. M. Zakeeruddin, L. Emsley, U. Rothlisberger, A. Hagfeldt, D. S. Kim, M. Grätzel, J. Y. Kim, Nature 2021, 592, 381.\",24.5,,,,,,,,,,α-FAPbI3,,,,,,,,,1.53,,,,79.1,26.1,,,,,,,1185\r\n\"P. Wang, B. Chen, R. Li, S. Wang, N. Ren, Y. Li, S. Mazumdar, B. Shi, Y. Zhao, X. Zhang, ACS Energy Lett. 2021, 6, 2121.\",23.4,,,,,,,,,,FA0.78MA0.22Pb(IBrCl)3,,,,,,,,,1.53,,,,79.3,24.6,,,,,,,1200\r\n\"M. Green, E. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 3.\",25.5,,,,,,,,,, ,,,,,,,,,1.53,,,,83.2,25.7,,,,,,,1189\r\n\"A. Y. Alsalloum, B. Turedi, X. Zheng, S. Mitra, A. A. Zhumekenov, K. J. Lee, P. Maity, I. Gereige, A. AlSaggaf, I. S. Roqan, O. F. Mohammed, O. M. Bakr, ACS Energy Lett. 2020, 5, 657.\",20.8,,,,,,,,,,MAPbI3 (sc),,,,,,,,,1.53,,,,77,23.9,,,,,,,1143\r\n\"M. Jeong, I. W. Choi, E. M. Go, Y. Cho, M. Kim, B. Lee, S. Jeong, Y. Jo, H. W. Choi, J. Lee, J.-H. Bae, S. K. Kwak, D. S. Kim, C. Yang, Science 2020, 369, 1615.\",24.6,,,,,,,,,,FAPbI3,,,,,,,,,1.54,,,,79.6,26.2,,,,,,,1181\r\n\"W. S. Yang, B.-W. Park, E. H. Jung, N. J. Jeon, Y. C. Kim, D. U. Lee, S. S. Shin, J. Seo, E. K. Kim, J. H. Noh, S. I. Seok, Science 2017, 356, 1376.\",22.1,,,,,,,,,,(FAPbI3)0.9(MAPbBr3)0.1,,,,,,,,,1.54,,,,80.3,25,,,,,,,1105\r\n\"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\",21.5,,,,,,,,,,Cs0.05FA0.70MA0.25PbI3-DAP,,,,,,,,,1.55,,,,79.2,23.4,,,,,,,1160\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\",25.2,,,,,,,,,, ,,,,,,,,,1.56,,,,84.8,24.1,,,,,,,1180\r\n\"J. J. Yoo, G. Seo, M. R. Chua, T. G. Park, Y. Lu, F. Rotermund, Y.-K. Kim, C. S. Moon, N. J. Jeon, J.-P. Correa-Baena, V. Bulović, S. S. Shin, M. G. Bawendi, J. Seo, Nature 2021, 590, 587.\",25.2,,,,,,,,,,FAMAPb(IBrCl)3,,,,,,,,,1.56,,,,84.8,25.1,,,,,,,1181\r\n\"J. J. Yoo, G. Seo, M. R. Chua, T. G. Park, Y. Lu, F. Rotermund, Y.-K. Kim, C. S. Moon, N. J. Jeon, J.-P. Correa-Baena, V. Bulović, S. S. Shin, M. G. Bawendi, J. Seo, Nature 2021, 590, 587.\",25.3,,,,,,,,,,FAMAPb(IBrCl)3,,,,,,,,,1.56,,,,84.6,25.1,,,,,,,1193\r\n\"G. Xu, R. Xue, S. J. Stuard, H. Ade, C. Zhang, J. Yao, Y. Li, Y. Li, Adv. Mater. 2021, 33, 2006753.\",21.9,,,,,,,,,,Rb0.05Cs0.05FA0.8MA0.1PbI2.85Br0.15,,,,,,,,,1.56,,,,81.4,24.4,,,,,,,1100\r\n\"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\",23,,,,,,,,,,Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3,,,,,,,,,1.57,,,,81.6,24.1,,,,,,,1170\r\n\"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\",22.3,,,,,,,,,,Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3,,,,,,,,,1.57,,,,82,23.8,,,,,,,1143\r\n\"S. Gharibzadeh, P. Fassl, I. Hossain, P. N. Rohrbeck, M. Frericks, M. Schmidt, T. Duong, M. R. Khan, T. Abzieher, B. Abdollahi Nejand, F. Schackmar, O. Almora, T. Feeney, R. Singh, D. Fuchs, U. Lemmer, J. P. Hofmann, S. Weber, U. W. Paetzold, Energy Environ. Sci. 2021, https://doi.org/10.1039/D1EE01508G.\",22.7,,,,,,,,,,Cs0.18FA0.82PbI3,,,,,,,,,1.57,,,,83.2,23.5,,,,,,,1162\r\n\"J. J. Yoo, S. Wieghold, M. C. Sponseller, M. R. Chua, S. N. Bertram, N. T. P. Hartono, J. S. Tresback, E. C. Hansen, J.-P. Correa-Baena, V. Bulović, T. Buonassisi, S. S. Shin, M. G. Bawendi, Energy Environ. Sci. 2019, 12, 2192.\",22.6,,,,,,,,,,(FAPbI3)0.92(MAPbBr3)0.08,,,,,,,,,1.58,,,,78.6,24.2,,,,,,,1186\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics Res. Appl. 2021, 29, 657.\",22.6,,,,,,,,,, ,,,,,,,,,1.58,,,,84.4,22.7,,,,,,,1178\r\n\"H. B. Lee, N. Kumar, M. M. Ovhal, Y. J. Kim, Y. M. Song, J.-W. Kang, Adv. Funct. Mater. 2020, n/a, 2001559.\",20.4,,,,,,,,,,Cs0.05(FAPbI3)0.85(MAPbBr3)0.15,,,,,,,,,1.58,,,,77.8,23.3,,,,,,,1125\r\n\"P. Cui, D. Wei, J. Ji, H. Huang, E. Jia, S. Dou, T. Wang, W. Wang, M. Li, Nat. Energy 2019, 4, 150.\",21.9,,,,,,,,,,FA0.15MA0.85PbI3,,,,,,,,,1.58,,,,80.6,24.2,,,,,,,1120\r\n\"M. Li, Z.-K. Wang, M.-P. Zhuo, Y. Hu, K.-H. Hu, Q.-Q. Ye, S. M. Jain, Y.-G. Yang, X.-Y. Gao, L.-S. Liao, Adv. Mater. 2018, 30, 1800258.\",21.1,,,,,,,,,,MAPb0.9Sn0.05Cu0.05I2.9Br0.1,,,,,,,,,1.59,,,,81,24,,,,,,,1086\r\n\"X. Zheng, B. Chen, J. Dai, Y. Fang, Y. Bai, Y. Lin, H. Wei, Xiao C. Zeng, J. Huang, Nat. Energy 2017, 2, 17102.\",21,,,,,,,,,,FA0.85MA0.15Pb(I0.85Br0.15)3,,,,,,,,,1.59,,,,77.7,23.7,,,,,,,1140\r\n\"Q. Cao, Y. Li, H. Zhang, J. Yang, J. Han, T. Xu, S. Wang, Z. Wang, B. Gao, J. Zhao, X. Li, X. Ma, M. Zakeeruddin Shaik, E. I. Sha Wei, X. Li, M. Grätzel, Sci. Adv.7, eabg0633.\",21.9,,,,,,,,,,CsMAFAPbI3:PPP,,,,,,,,,1.6,,,,83.7,23.1,,,,,,,1131\r\n\"L. Wang, H. Zhou, J. Hu, B. Huang, M. Sun, B. Dong, G. Zheng, Y. Huang, Y. Chen, L. Li, Z. Xu, N. Li, Z. Liu, Q. Chen, L.-D. Sun, C.-H. Yan, Science 2019, 363, 265.\",20.3,,,,,,,,,,MAPbI3−xClx,,,,,,,,,1.6,,,,77.4,23.2,,,,,,,1130\r\n\"S. Xiong, Z. Hou, S. Zou, X. Lu, J. Yang, T. Hao, Z. Zhou, J. Xu, Y. Zeng, W. Xiao, W. Dong, D. Li, X. Wang, Z. Hu, L. Sun, Y. Wu, X. Liu, L. Ding, Z. Sun, M. Fahlman, Q. Bao, Joule 2021, 5, 467.\",21.4,,,,,,,,,,MAPbI3,,,,,,,,,1.61,,,,82.9,23.1,,,,,,,1120\r\n\"J. Peng, D. Walter, Y. Ren, M. Tebyetekerwa, Y. Wu, T. Duong, Q. Lin, J. Li, T. Lu, A. Mahmud Md, C. Lem Olivier Lee, S. Zhao, W. Liu, Y. Liu, H. Shen, L. Li, F. Kremer, T. Nguyen Hieu, D.-Y. Choi, J. Weber Klaus, R. Catchpole Kylie, P. White Thomas, Science 2021, 371, 390.\",21.5,,,,,,,,,,Cs0.05FA0.88MA0.07PbI2.56Br0.44,,,,,,,,,1.61,,,,83.6,21.6,,,,,,,1192\r\n\"J. Peng, D. Walter, Y. Ren, M. Tebyetekerwa, Y. Wu, T. Duong, Q. Lin, J. Li, T. Lu, A. Mahmud Md, C. Lem Olivier Lee, S. Zhao, W. Liu, Y. Liu, H. Shen, L. Li, F. Kremer, T. Nguyen Hieu, D.-Y. Choi, J. Weber Klaus, R. Catchpole Kylie, P. White Thomas, Science 2021, 371, 390.\",23.2,,,,,,,,,,Cs0.05FA0.88MA0.07PbI2.56Br0.44,,,,,,,,,1.61,,,,84.5,22.1,,,,,,,1240\r\n\"M. A. Mahmud, T. Duong, Y. Yin, H. T. Pham, D. Walter, J. Peng, Y. Wu, L. Li, H. Shen, N. Wu, N. Mozaffari, G. Andersson, K. R. Catchpole, K. J. Weber, T. P. White, Adv. Funct. Mater. 2020, 30, 1907962.\",22.6,,,,,,,,,,Cs0.07Rb0.03FA0.765MA0.135PbI2.55Br0.45,,,,,,,,,1.61,,,,78.5,24,,,,,,,1200\r\n\"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\",21.7,,,,,,,,,,MAPbI3-DAP,,,,,,,,,1.62,,,,81.7,22.5,,,,,,,1180\r\n\"K. Choi, J. Lee, H. I. Kim, C. W. Park, G.-W. Kim, H. Choi, S. Park, S. A. Park, T. Park, Energy Environ. Sci. 2018, 11, 3238.\",20.3,,,,,,,,,,Cs0.05FA0.76MA0.19PbBr0.6I2.4,,,,,,,,,1.63,,,,76.8,23.4,,,,,,,1130\r\n\"X. Zhao, C. Yao, T. Liu, J. C. HamillJr, G. O. Ngongang Ndjawa, G. Cheng, N. Yao, H. Meng, Y.-L. Loo, Adv. Mater. 2019, 31, 1904494.\",20.4,,,,,,,,,,Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3,,,,,,,,,1.64,,,,75.8,23.6,,,,,,,1140\r\n\"N. J. Jeon, J. H. Noh, Y. C. Kim, W. S. Yang, S. Ryu, S. I. Seok, Nat. Mater. 2014, 13, 897.\",16.2,,,,,,,,,,MAPbI1−xBrx,,,,,,,,,1.65,,,,74.2,19.6,,,,,,,1109\r\n\"J. H. Noh, S. H. Im, J. H. Heo, T. N. Mandal, S. I. Seok, Nano Lett. 2013, 13, 1764.\",10.4,,,,,,,,,,MAPb(I0.87Br0.13)3,,,,,,,,,1.66,,,,70.4,16.3,,,,,,,904\r\n\"Y. Yang, C. Liu, O. A. Syzgantseva, M. A. Syzgantseva, S. Ma, Y. Ding, M. Cai, X. Liu, S. Dai, M. K. Nazeeruddin, Adv. Energy Mater. 2021, 11, 2002966.\",17.9,,,,,,,,,,(PEA)2(MA)3Pb4I13:NH4I0.2Cl0.8,,,,,,,,,1.67,,,,81.9,18.4,,,,,,,1190\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",20.7,,,,,,,,,,Cs0.05MA0.15FA0.8Pb(I0.75Br0.25)3,,,,,,,,,1.68,,,,79.7,21.3,,,,,,,1220\r\n\"M. Chen, M.-G. Ju, H. F. Garces, A. D. Carl, L. K. Ono, Z. Hawash, Y. Zhang, T. Shen, Y. Qi, R. L. Grimm, D. Pacifici, X. C. Zeng, Y. Zhou, N. P. Padture, Nat. Commun. 2019, 10, 16.\",7.1,,,,,,,,,,MAPb(I0.74Br0.26)3,,,,,,,,,1.69,,,,63,10.4,,,,,,,936\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",16.9,,,,,,,,,,Cs0.2FA0.8Pb(I0.75Br0.25)3,,,,,,,,,1.7,,,,71.5,20.2,,,,,,,1170\r\n\"H. Wang, H. Liu, Z. Dong, W. Li, L. Zhu, H. Chen, Nano Energy 2021, 84, 105881.\",14.6,,,,,,,,,,CsPbI3,,,,,,,,,1.71,,,,79,17.5,,,,,,,1056\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",18.6,,,,,,,,,,FA0.17Cs0.83PbI2.2Br0.8,,,,,,,,,1.72,,,,77.9,19.2,,,,,,,1244\r\n\"Z. Liu, J. Siekmann, B. Klingebiel, U. Rau, T. Kirchartz, Adv. Energy Mater. 2021, 11, 2003386.\",18.3,,,,,,,,,,MAPbI2.4Br0.6,,,,,,,,,1.72,,,,77,17.6,,,,,,,1350\r\n\"D. P. McMeekin, G. Sadoughi, W. Rehman, G. E. Eperon, M. Saliba, M. T. Hörantner, A. Haghighirad, N. Sakai, L. Korte, B. Rech, M. B. Johnston, L. M. Herz, H. J. Snaith, Science 2016, 351, 151.\",17.1,,,,,,,,,,FA0.83Cs0.17Pb(I0.6Br0.4)3,,,,,,,,,1.72,,,,73.5,19.4,,,,,,,1200\r\n\"T. Duong, H. Pham, T. C. Kho, P. Phang, K. C. Fong, D. Yan, Y. Yin, J. Peng, M. A. Mahmud, S. Gharibzadeh, B. A. Nejand, I. M. Hossain, M. R. Khan, N. Mozaffari, Y. Wu, H. Shen, J. Zheng, H. Mai, W. Liang, C. Samundsett, M. Stocks, K. McIntosh, G. G. Andersson, U. Lemmer, B. S. Richards, U. W. Paetzold, A. Ho-Ballie, Y. Liu, D. Macdonald, A. Blakers, J. Wong-Leung, T. White, K. Weber, K. Catchpole, Adv. Energy Mater. 2020, 10, 1903553.\",18.3,,,,,,,,,,Rb0.05Cs0.095MA0.1425FA0.7125PbI2Br,,,,,,,,,1.74,,,,76.3,18.9,,,,,,,1269\r\n\"S. Gharibzadeh, B. Abdollahi Nejand, M. Jakoby, T. Abzieher, D. Hauschild, S. Moghadamzadeh, J. A. Schwenzer, P. Brenner, R. Schmager, A. A. Haghighirad, L. Weinhardt, U. Lemmer, B. S. Richards, I. A. Howard, U. W. Paetzold, Adv. Energy Mater. 2019, 9, 1803699.\",19.8,,,,,,,,,,FA0.83Cs0.17Pb(I0.6Br0.4)3,,,,,,,,,1.75,,,,78,19.4,,,,,,,1310\r\n\"Y. Lin, B. Chen, F. Zhao, X. Zheng, Y. Deng, Y. Shao, Y. Fang, Y. Bai, C. Wang, J. Huang, Adv. Mater. 2017, 29, 1700607.\",18.5,,,,,,,,,,(FA0.83MA0.17)0.95Cs0.05Pb(I0.6Br0.4)3,,,,,,,,,1.76,,,,76.4,20,,,,,,,1210\r\n\"Q. Ye, Y. Zhao, S. Mu, F. Ma, F. Gao, Z. Chu, Z. Yin, P. Gao, X. Zhang, J. You, Adv. Mater. 2019, 31, 1905143.\",18.6,,,,,,,,,,CsPbI3−xBrx,,,,,,,,,1.77,,,,82.5,18.3,,,,,,,1234\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",15.7,,,,,,,,,,Cs0.17FA0.83Pb(I0.6Br0.4)3,,,,,,,,,1.78,,,,70.5,18.4,,,,,,,1210\r\n\"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorović, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\",19,,,,,,,,,,Cs0.12MA0.05FA0.83Pb(I0.6Br0.4)3,,,,,,,,,1.79,,,,80,19,,,,,,,1250\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",16.5,,,,,,,,,,Cs0.17FA0.83PbI1.8Br1.2,,,,,,,,,1.79,,,,74.8,17.2,,,,,,,1284\r\n\"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\",13.7,,,,,,,,,,MAPbBrI2,,,,,,,,,1.8,,,,75,14.4,,,,,,,1272\r\n\"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\",16.3,,,,,,,,,,FA0.6Cs0.4Pb(I0.65Br0.35)3,,,,,,,,,1.81,,,,78.6,17,,,,,,,1220\r\n\"Y.-N. Zhang, B. Li, L. Fu, Y. Zou, Q. Li, L.-W. Yin, Sol. Energy Mater. Sol. Cells 2019, 194, 168.\",17.1,,,,,,,,,,FAPbI1.5Br1.5/CsPbI1.5Br1.5,,,,,,,,,1.82,,,,74,21,,,,,,,1100\r\n\"M. Chen, M.-G. Ju, A. D. Carl, Y. Zong, R. L. Grimm, J. Gu, X. C. Zeng, Y. Zhou, N. P. Padture, Joule 2018, 2, 558.\",3.3,,,,,,,,,,Cs2TiBr6,,,,,,,,,1.83,,,,56.9,5.7,,,,,,,1020\r\n\"M.-J. Wu, C.-C. Kuo, L.-S. Jhuang, P.-H. Chen, Y.-F. Lai, F.-C. Chen, Adv. Energy Mater. 2019, 9, 1901863.\",8.6,,,,,,,,,,MA0.85Cs0.15Pb(I0.65Br0.35)3,,,,,,,,,1.83,,,,68.4,11.3,,,,,,,1110\r\n\"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\",15.2,,,,,,,,,,Cs0.2FA0.8Pb(I0.6Br0.4)3-DAP,,,,,,,,,1.84,,,,77.3,15.6,,,,,,,1260\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",15,,,,,,,,,,Cs0.17FA0.83PbI1.5Br1.5,,,,,,,,,1.85,,,,74.2,15.6,,,,,,,1296\r\n\"J. Zhang, Z. Wang, A. Mishra, M. Yu, M. Shasti, W. Tress, D. J. Kubicki, C. E. Avalos, H. Lu, Y. Liu, B. I. Carlsen, A. Agarwalla, Z. Wang, W. Xiang, L. Emsley, Z. Zhang, M. Grätzel, W. Guo, A. Hagfeldt, Joule 2020, 4, 222.\",17,,,,,,,,,,CsPb(I0.75Br0.25)3-0.5FAOAc,,,,,,,,,1.86,,,,79.8,15.9,,,,,,,1340\r\n\"W. Xiang, Z. Wang, D. J. Kubicki, X. Wang, W. Tress, J. Luo, J. Zhang, A. Hofstetter, L. Zhang, L. Emsley, M. Grätzel, A. Hagfeldt, Nat. Commun. 2019, 10, 4686.\",14,,,,,,,,,,CsPb0.8Ba0.2I2Br,,,,,,,,,1.87,,,,78.1,14,,,,,,,1280\r\n\"W. Xiang, Z. Wang, D. J. Kubicki, W. Tress, J. Luo, D. Prochowicz, S. Akin, L. Emsley, J. Zhou, G. Dietler, M. Grätzel, A. Hagfeldt, Joule 2019, 3, 205.\",13.7,,,,,,,,,,CsPb0.95Eu0.05I2Br,,,,,,,,,1.87,,,,76.8,14.6,,,,,,,1220\r\n\"H. Zhao, Z. Xu, Y. Che, Y. Han, S. Yang, C. Duan, J. Cui, S. Dai, Z. Liu, S. Liu, J. Power Sources 2021, 492, 229580.\",15.9,,,,,,,,,,CsPbI2Br,,,,,,,,,1.88,,,,79.1,15.5,,,,,,,1300\r\n\"S. Yang, H. Zhao, Y. Han, C. Duan, Z. Liu, S. Liu, Small 2019, 15, 1904387.\",15.3,,,,,,,,,,CsPbI2Br,,,,,,,,,1.88,,,,79,15.4,,,,,,,1250\r\n\"J. Li, J. Yang, J. Ma, J. Liang, Y. Liu, X. Hu, C. Chen, W. Yang, J. Min, Q. Bao, G. Fang, C. Tao, Chem. Eng. J. 2021, 417, 129247.\",16,,,,,,,,,,CsPbI2Br,,,,,,,,,1.89,,,,77.5,15.8,,,,,,,1310\r\n\"H. Zhao, Y. Han, Z. Xu, C. Duan, S. Yang, S. Yuan, Z. Yang, Z. Liu, S. Liu, Adv. Energy Mater. 2019, 9, 1902279.\",15.6,,,,,,,,,,CsPbI2−xBr(Ac)x,,,,,,,,,1.89,,,,78.3,15.3,,,,,,,1300\r\n\"S. S. Mali, J. V. Patil, J. A. Steele, S. R. Rondiya, N. Y. Dzade, C. K. Hong, ACS Energy Lett. 2021, 6, 778.\",15,,,,,,,,,,InCl3:CsPbI2Br,,,,,,,,,1.9,,,,75.6,16,,,,,,,1240\r\n\"C. Duan, J. Cui, M. Zhang, Y. Han, S. Yang, H. Zhao, H. Bian, J. Yao, K. Zhao, Z. Liu, S. Liu, Adv. Energy Mater. 2020, 10, 2000691.\",16.1,,,,,,,,,,CsPbI2Br,,,,,,,,,1.9,,,,79.7,15.3,,,,,,,1320\r\n\"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\",14.4,,,,,,,,,,FA0.17Cs0.83PbI1.2Br1.8,,,,,,,,,1.91,,,,70.1,15.6,,,,,,,1312\r\n\"X. Pu, J. Han, S. Wang, H. Zhou, Q. Cao, J. Yang, Z. He, X. Li, J. Materiomics 2021, 7, 1039.\",14.2,,,,,,,,,,CsPbI2Br,,,,,,,,,1.91,,,,77.9,15.7,,,,,,,1160\r\n\"K. M. Boopathi, P. Karuppuswamy, A. Singh, C. Hanmandlu, L. Lin, S. A. Abbas, C. C. Chang, P. C. Wang, G. Li, C. W. Chu, J. Mater. Chem. A 2017, 5, 20843.\",2,,,,,,,,,,MA3Sb2I9+HI,,,,,,,,,1.91,,,,60.8,5.4,,,,,,,620\r\n\"I. Turkevych, S. Kazaoui, E. Ito, T. Urano, K. Yamada, H. Tomiyasu, H. Yamagishi, M. Kondo, S. Aramaki, ChemSusChem 2017, 10, 3754.\",4.3,,,,,,,,,,Ag3BiI6,,,,,,,,,1.94,,,,63.8,10.7,,,,,,,630\r\n\"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\",2.2,,,,,,,,,,AgBiI4,,,,,,,,,1.94,,,,62.7,5.2,,,,,,,670\r\n\"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\",2.6,,,,,,,,,,AgBiI5,,,,,,,,,1.95,,,,62.4,6,,,,,,,690\r\n\"B.-W. Park, B. Philippe, X. Zhang, H. Rensmo, G. Boschloo, E. M. J. Johansson, Adv. Mater. 2015, 27, 6806.\",1.1,,,,,,,,,,Cs3Bi2I9,,,,,,,,,1.97,,,,59.6,2.2,,,,,,,850\r\n\"J. Liang, P. Zhao, C. Wang, Y. Wang, Y. Hu, G. Zhu, L. Ma, J. Liu, Z. Jin, J. Am. Chem. Soc. 2017, 139, 14009.\",8.3,,,,,,,,,,CsPbIBr2,,,,,,,,,1.98,,,,62,12.3,,,,,,,1080\r\n\"D. Forgács, L. Gil-Escrig, D. Pérez-Del-Rey, C. Momblona, J. Werner, B. Niesen, C. Ballif, M. Sessolo, H. J. Bolink, Adv. Energy Mater. 2017, 7, 1602121.\",9.6,,,,,,,,,,Cs0.15FA0.85Pb(I0.3Br0.7)3,,,,,,,,,2,,,,72.3,11.2,,,,,,,1185\r\n\"S. A. Kulkarni, T. Baikie, P. P. Boix, N. Yantara, N. Mathews, S. Mhaisalkar, J. Mater. Chem. A 2014, 2, 9221.\",2.8,,,,,,,,,,MAPb(I0.41Br0.59)3,,,,,,,,,2.03,,,,52.7,6.4,,,,,,,836\r\n\"Q. Xue, G. Chen, M. Liu, J. Xiao, Z. Chen, Z. Hu, X.-F. Jiang, B. Zhang, F. Huang, W. Yang, H.-L. Yip, Y. Cao, Adv. Energy Mater. 2016, 6, 1502021.\",10.3,,,,,,,,,,MAPb(I0.3Br0.7)xCl3−x(Br),,,,,,,,,2.04,,,,79.2,9.7,,,,,,,1340\r\n\"Y. Zhao, A. M. Nardes, K. Zhu, Faraday Discuss. 2014, 176, 301.\",6.1,,,,,,,,,,MAPbIBr2,,,,,,,,,2.05,,,,77.1,5.4,,,,,,,1450\r\n\"H. Wang, S. Cao, B. Yang, H. Li, M. Wang, X. Hu, K. Sun, Z. Zang, Sol. RRL 2020, 4, 1900363.\",10.2,,,,,,,,,,CsPbIBr2,,,,,,,,,2.09,,,,69.4,11.5,,,,,,,1270\r\n\"W. Zhu, Z. Zhang, W. Chai, Q. Zhang, D. Chen, Z. Lin, J. Chang, J. Zhang, C. Zhang, Y. Hao, ChemSusChem 2019, 12, 2318.\",10.7,,,,,,,,,,CsPbIBr2,,,,,,,,,2.1,,,,72,11.8,,,,,,,1261\r\n\"B. Zhang, W. Bi, Y. Wu, C. Chen, H. Li, Z. Song, Q. Dai, L. Xu, H. Song, ACS Appl. Mater. Interfaces 2019, 11, 33868.\",9.2,,,,,,,,,,GAI-DEE-CsPbIBr2,,,,,,,,,2.11,,,,74.6,10.2,,,,,,,1200\r\n\"R. Nie, A. Mehta, B.-w. Park, H.-W. Kwon, J. Im, S. I. Seok, J. Am. Chem. Soc. 2018, 140, 872.\",3.1,,,,,,,,,,MASbSI2,,,,,,,,,2.14,,,,58.4,8.1,,,,,,,650\r\n\"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\",4.4,,,,,,,,,,(FA0.85MA0.15Pb(I0.85Br0.15)3) R = 0.7,,,,,,,,,2.15,,,,64.8,6.3,,,,,,,1084\r\n\"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\",2,,,,,,,,,,(FA0.85MA0.15Pb(I0.85Br0.15)3) R = 0.56,,,,,,,,,2.19,,,,69.5,3,,,,,,,1051\r\n\"F. Umar, J. Zhang, Z. Jin, I. Muhammad, X. Yang, H. Deng, K. Jahangeer, Q. Hu, H. Song, J. Tang, Adv. Opt. Mater. 2019, 7, 1801368.\",1.2,,,,,,,,,,Cs3Sb2I9,,,,,,,,,2.2,,,,55.9,3.6,,,,,,,610\r\n\"Y. Zhang, Y. Liang, Y. Wang, F. Guo, L. Sun, D. Xu, ACS Energy Lett. 2018, 3, 1808.\",10.6,,,,,,,,,,FAPbBr3,,,,,,,,,2.27,,,,76.5,8.9,,,,,,,1552\r\n\"J. Duan, Y. Zhao, B. He, Q. Tang, Angew. Chem., Int. Ed. 2018, 57, 3787.\",9.7,,,,,,,,,,CsPbBr3,,,,,,,,,2.31,,,,81.9,8.1,,,,,,,1458\r\n\"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\",10.1,,,,,,,,,,MAPbBr3,,,,,,,,,2.32,,,,79.1,7.7,,,,,,,1653\r\n\"M. Wang, J. Duan, J. Du, X. Yang, Y. Duan, T. Zhang, Q. Tang, ACS Appl. Mater. Interfaces 2021, 13, 12091.\",8.5,,,,,,,,,,CsPbBr3,,,,,,,,,2.33,,,,82,6.6,,,,,,,1580\r\n\"G. Liao, J. Duan, Y. Zhao, Q. Tang, Sol. Energy 2018, 171, 279=.\",8.2,,,,,,,,,,CsPbBr3,,,,,,,,,2.33,,,,76.1,7.3,,,,,,,1470\r\n\"X. Sun, B. He, J. Zhu, R. Zhu, H. Chen, Y. Duan, Q. Tang, Chem. Eng. J. 2021, 412, 128727.\",10.1,,,,,,,,,,CsPbBr3,,,,,,,,,2.34,,,,80,7.9,,,,,,,1602\r\n\"J. Zhu, B. He, Z. Gong, Y. Ding, W. Zhang, X. Li, Z. Zong, H. Chen, Q. Tang, ChemSusChem 2020, 13, 1834.\",9.7,,,,,,,,,,CsPbBr3,,,,,,,,,2.34,,,,82.8,7.4,,,,,,,1584\r\n\"Y. Zhao, J. Duan, Y. Wang, X. Yang, Q. Tang, Nano Energy 2020, 67, 104286.\",10.7,,,,,,,,,,CsPbBr3,,,,,,,,,2.35,,,,83.5,7.9,,,,,,,1622\r\n\"Y. Zhao, J. Duan, H. Yuan, Y. Wang, X. Yang, B. He, Q. Tang, Sol. RRL 2019, 3, 1800284.\",10.6,,,,,,,,,,CsSnBr3,,,,,,,,,2.35,,,,84.4,7.8,,,,,,,1610\r\n\"C. H. Ng, T. S. Ripolles, K. Hamada, S. H. Teo, H. N. Lim, J. Bisquert, S. Hayase, Sci. Rep. 2018, 8, 2482.\",4,,,,,,,,,,CsPbBr2.9I0.1,,,,,,,,,2.36,,,,63.6,5.5,,,,,,,1130\r\n\"F. Jiang, D. Yang, Y. Jiang, T. Liu, X. Zhao, Y. Ming, B. Luo, F. Qin, J. Fan, H. Han, L. Zhang, Y. Zhou, J. Am. Chem. Soc. 2018, 140, 1019.\",2.2,,,,,,,,,,MA3Sb2ClxI9−x,,,,,,,,,2.37,,,,63.5,5,,,,,,,690\r\n\"X. Wan, Z. Yu, W. Tian, F. Huang, S. Jin, X. Yang, Y.-B. Cheng, A. Hagfeldt, L. Sun, J. Energy Chem. 2020, 46, 8.\",8.1,,,,,,,,,,CsPbBr3,,,,,,,,,2.38,,,,78.8,6.9,,,,,,,1490\r\n\"Y. Zhao, H. Xu, Y. Wang, X. Yang, J. Duan, Q. Tang, J. Power Sources 2019, 440, 227151.\",10.3,,,,,,,,,,Cs0.91Rb0.09PbBr3,,,,,,,,,2.39,,,,80,8.2,,,,,,,1580\r\n\"X. Yang, Y. Chen, P. Liu, H. Xiang, W. Wang, R. Ran, W. Zhou, Z. Shao, Adv. Funct. Mater. 2020, 30, 2001557.\",2.7,,,,,,,,,,Cs2AgBiBr6,,,,,,,,,2.41,,,,51.2,5.2,,,,,,,1020\r\n\"M. Safdari, P. H. Svensson, M. T. Hoang, I. Oh, L. Kloo, J. M. Gardner, J. Mater. Chem. A 2016, 4, 15638.\",1.1,,,,,,,,,,BdAPbI4,,,,,,,,,2.42,,,,43,2.9,,,,,,,870\r\n\"G. Murugadoss, R. Thangamuthu, S. M. Senthil Kumar, N. Anandhan, M. Rajesh Kumar, A. Rathishkumar, J. Alloys Compd. 2019, 787, 17.\",2.8,,,,,,,,,,CsPb2Br5,,,,,,,,,2.43,,,,60.3,5.7,,,,,,,820\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",2.4,,,,,,,,,,FAPbBr2.1Cl0.9,,,,,,,,,2.44,,,,60.9,3.4,,,,,,,1140\r\n\"B. Wang, N. Li, L. Yang, C. Dall'Agnese, A. K. Jena, S.-i. Sasaki, T. Miyasaka, H. Tamiaki, X.-F. Wang, J. Am. Chem. Soc. 2021, 143, 2207.\",2.9,,,,,,,,,,Cs2AgBiBr6,,,,,,,,,2.45,,,,70.9,4.1,,,,,,,1010\r\n\"E. Greul, Michiel L. Petrus, A. Binek, P. Docampo, T. Bein, J. Mater. Chem. A 2017, 5, 19972.\",1.7,,,,,,,,,,Cs2AgBiBr6,,,,,,,,,2.46,,,,40.2,3.9,,,,,,,1060\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",1.4,,,,,,,,,,FAPbBr2Cl,,,,,,,,,2.48,,,,52,2.5,,,,,,,1060\r\n\"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\",10.6,,,,,,,PTB7-Th:IEICO-4F,,,,,,,,,,,,1.32,,,,63.2,24.3,,,,,,,690\r\n\"X. Song, N. Gasparini, L. Ye, H. Yao, J. Hou, H. Ade, D. Baran, ACS Energy Lett. 2018, 3, 669.\",12.8,,,,,,,PTB7-Th:IEICO-4F,,,,,,,,,,,,1.34,,,,65.9,27.3,,,,,,,712\r\n\"X. Song, N. Gasparini, M. M. Nahid, S. H. K. Paleti, C. Li, W. Li, H. Ade, D. Baran, Adv. Funct. Mater. 2019, 29, 1902441.\",9.7,,,,,,,PBDTT-DPP:IEICO-4F,,,,,,,,,,,,1.34,,,,70.2,19.8,,,,,,,695\r\n\"F. Qi, K. Jiang, F. Lin, Z. Wu, H. Zhang, W. Gao, Y. Li, Z. Cai, H. Y. Woo, Z. Zhu, A. K. Y. Jen, ACS Energy Lett. 2021, 6, 9.\",17,,,,,,,PM6:mBzS-4F,,,,,,,,,,,,1.35,,,,76.4,27.2,,,,,,,804\r\n\"S. M. Hosseini, N. Tokmoldin, Y. W. Lee, Y. Zou, H. Y. Woo, D. Neher, S. Shoaee, Sol. RRL 2020, 4, 2000498.\",15.9,,,,,,,PM6:Y6,,,,,,,,,,,,1.35,,,,73.4,26.3,,,,,,,820\r\n\"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\",14.3,,,,,,,PBDB-T-2Cl:BTP-4F:PC61BM,,,,,,,,,,,,1.35,,,,66.5,26.8,,,,,,,802\r\n\"S. Liu, J. Yuan, W. Deng, M. Luo, Y. Xie, Q. Liang, Y. Zou, Z. He, H. Wu, Y. Cao, Nat. Photonics 2020, 14, 300.\",15.9,,,,,,,PM6:Y11,,,,,,,,,,,,1.36,,,,74.1,25.4,,,,,,,846\r\n\"Y. Lin, M. I. Nugraha, Y. Firdaus, A. D. Scaccabarozzi, F. Aniés, A.-H. Emwas, E. Yengel, X. Zheng, J. Liu, W. Wahyudi, E. Yarali, H. Faber, O. M. Bakr, L. Tsetseris, M. Heeney, T. D. Anthopoulos, ACS Energy Lett. 2020, 5, 3663.\",18.3,,,,,,,PM6:BTP-eC9:PC71BM,,,,,,,,,,,,1.37,,,,79.4,26.9,,,,,,,856\r\n\"L. Arunagiri, Z. Peng, X. Zou, H. Yu, G. Zhang, Z. Wang, J. Y. Lin Lai, J. Zhang, Y. Zheng, C. Cui, F. Huang, Y. Zou, K. S. Wong, P. C. Y. Chow, H. Ade, H. Yan, Joule 2020, 4, 1790.\",17.7,,,,,,,PM6:PTQ10:PC71BM:N3,,,,,,,,,,,,1.38,,,,77.7,26.8,,,,,,,852\r\n\"Y. Cui, H. Yao, J. Zhang, K. Xian, T. Zhang, L. Hong, Y. Wang, Y. Xu, K. Ma, C. An, C. He, Z. Wei, F. Gao, J. Hou, Adv. Mater. 2020, 32, 1908205.\",17.3,,,,,,,PBDB-TF:BTP-eC9,,,,,,,,,,,,1.38,,,,78.5,26.2,,,,,,,841\r\n\"Q. Liu, Y. Jiang, K. Jin, J. Qin, J. Xu, W. Li, J. Xiong, J. Liu, Z. Xiao, K. Sun, S. Yang, X. Zhang, L. Ding, Sci. Bull. 2020, 65, 272.\",18.2,,,,,,,D18:Y6,,,,,,,,,,,,1.39,,,,76.6,27.7,,,,,,,859\r\n\"Y. Cui, H. Yao, L. Hong, T. Zhang, Y. Tang, B. Lin, K. Xian, B. Gao, C. An, P. Bi, W. Ma, J. Hou, Natl. Sci. Rev. 2019, 7, 1239.\",17,,,,,,,PBDB-TF:BTP-4Cl-12,,,,,,,,,,,,1.39,,,,25.5,77.6,,,,,,,858\r\n\"H. Chen, H. Lai, Z. Chen, Y. Zhu, H. Wang, L. Han, Y. Zhang, F. He, Angew. Chem., Int. Ed. 2021, 60, 3238.\",17.1,,,,,,,BTIC-2Cl-γCF3: PC71ThBM: PBDB-TF,,,,,,,,,,,,1.39,,,,78.1,25.8,,,,,,,850\r\n\"X. Guo, Q. Fan, J. Wu, G. Li, Z. Peng, W. Su, J. Lin, L. Hou, Y. Qin, H. Ade, L. Ye, M. Zhang, Y. Li, Angew. Chem., Int. Ed. 2021, 60, 2322.\",17.6,,,,,,,PM6-Tz20: Y6,,,,,,,,,,,,1.4,,,,75,27.3,,,,,,,860\r\n\"L. Liu, Y. Kan, K. Gao, J. Wang, M. Zhao, H. Chen, C. Zhao, T. Jiu, A.-K.-Y. Jen, Y. Li, Adv. Mater. 2020, 32, 1907604.\",17.1,,,,,,,PM6:Y6,,,,,,,,,,,,1.4,,,,77.6,26.4,,,,,,,834\r\n\"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\",16.5,,,,,,,PBDB-TF:BTP-4Cl,,,,,,,,,,,,1.4,,,,75,25.4,,,,,,,867\r\n\"C. Xu, X. Ma, Z. Zhao, M. Jiang, Z. Hu, J. Gao, Z. Deng, Z. Zhou, Q. An, J. Zhang, F. Zhang, Sol. RRL 2021, 5, 2100175.\",17.6,,,,,,,D18-Cl:PM6:Y6,,,,,,,,,,,,1.41,,,,76.8,26.4,,,,,,,871\r\n\"X. Liao, Q. He, G. Zhou, X. Xia, P. Zhu, Z. Xing, H. Zhu, Z. Yao, X. Lu, Y. Chen, Chem. Mater. 2021, 33, 430.\",17.1,,,,,,,PM6:Y6:DFBT-TT6,,,,,,,,,,,,1.41,,,,76,26.6,,,,,,,845\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\",17.4,,,,,,, ,,,,,,,,,,,,1.41,,,,77.9,25.8,,,,,,,862\r\n\"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\",15.6,,,,,,,PBDB-TF:BTP-4F,,,,,,,,,,,,1.42,,,,75.1,24.9,,,,,,,834\r\n\"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\",15.6,,,,,,, ,,,,,,,,,,,,1.42,,,,74.4,25,,,,,,,838\r\n\"Q. Guo, J. Lin, H. Liu, X. Dong, X. Guo, L. Ye, Z. Ma, Z. Tang, H. Ade, M. Zhang, Y. Li, Nano Energy 2020, 74, 104861.\",14.3,,,,,,,PM6:IDST-4F,,,,,,,,,,,,1.43,,,,70,24.9,,,,,,,820\r\n\"T. Liu, T. Yang, R. Ma, L. Zhan, Z. Luo, G. Zhang, Y. Li, K. Gao, Y. Xiao, J. Yu, X. Zou, H. Sun, M. Zhang, T. A. Dela Peña, Z. Xing, H. Liu, X. Li, G. Li, J. Huang, C. Duan, K. S. Wong, X. Lu, X. Guo, F. Gao, H. Chen, F. Huang, Y. Li, Y. Li, Y. Cao, B. Tang, H. Yan, Joule 2021, 5, 914.\",16.1,,,,,,,PM6:PY-IT:BN-T,,,,,,,,,,,,144,,,,74.3,22.7,,,,,,,955\r\n\"H. Lai, Q. Zhao, Z. Chen, H. Chen, P. Chao, Y. Zhu, Y. Lang, N. Zhen, D. Mo, Y. Zhang, F. He, Joule 2020, 4, 688.\",13.6,,,,,,,PBDB-TF:BTIC-F-m,,,,,,,,,,,,1.44,,,,69.1,21.4,,,,,,,920\r\n\"M. Green, E. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 3.\",18.2,,,,,,, ,,,,,,,,,,,,1.46,,,,78.9,25.7,,,,,,,897\r\n\"K. Jiang, Q. Wei, J. Y. L. Lai, Z. Peng, H. K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Joule 2019, 3, 3020.\",12.9,,,,,,,PM6:N-C11,,,,,,,,,,,,1.46,,,,70.6,21.5,,,,,,,852\r\n\"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\",14.6,,,,,,,PBDB-T-2Cl:BP-4F:MF1,,,,,,,,,,,,1.47,,,,71.7,23.1,,,,,,,882\r\n\"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\",12.4,,,,,,,PBDB-T:IDT-EDOT:PC71BM,,,,,,,,,,,,1.48,,,,67.7,20.8,,,,,,,880\r\n\"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\",15.4,,,,,,,PM6:DTTC-4Cl,,,,,,,,,,,,1.5,,,,74.1,22.6,,,,,,,920\r\n\"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\",13.3,,,,,,,PM6:SeTlC4Cl-DIO,,,,,,,,,,,,1.51,,,,75,22.9,,,,,,,780\r\n\"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\",10.4,,,,,,,PBDB-T:IDT-EDOT:PC71BM,,,,,,,,,,,,1.52,,,,68,18,,,,,,,850\r\n\"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\",10.7,,,,,,,PM6:SeTlC4Cl,,,,,,,,,,,,1.53,,,,56.7,22.2,,,,,,,850\r\n\"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\",13.6,,,,,,,BTR:NITI:PC71BM,,,,,,,,,,,,1.54,,,,73.8,19.5,,,,,,,940\r\n\"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\",12,,,,,,,PM6:IT-4F,,,,,,,,,,,,1.55,,,,73.3,19.5,,,,,,,840\r\n\"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\",12.1,,,,,,,PBDB-T-2F:IT-4F,,,,,,,,,,,,1.56,,,,70.1,20.9,,,,,,,826\r\n\"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\",13.9,,,,,,,PM6:DTTC-4F,,,,,,,,,,,,1.58,,,,67.4,21.7,,,,,,,950\r\n\"Y. Lin, B. Adilbekova, Y. Firdaus, E. Yengel, H. Faber, M. Sajjad, X. Zheng, E. Yarali, A. Seitkhan, O. M. Bakr, A. El-Labban, U. Schwingenschlögl, V. Tung, I. McCulloch, F. Laquai, T. D. Anthopoulos, Adv. Mater. 2019, 31, 1902965.\",13.5,,,,,,,PBDB-T-SF:IT-4F,,,,,,,,,,,,1.58,,,,74.53,20.6,,,,,,,880\r\n\"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\",13.4,,,,,,,PM6:DTC-4F,,,,,,,,,,,,1.61,,,,70.5,20.2,,,,,,,940\r\n\"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\",12.1,,,,,,,PBDB-T-2Cl:MF1,,,,,,,,,,,,1.61,,,,73,18.1,,,,,,,916\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\",11,,,,,,, ,,,,,,,,,,,,1.62,,,,71.5,19.4,,,,,,,793\r\n\"Z. Luo, C. Sun, S. Chen, Z.-G. Zhang, K. Wu, B. Qiu, C. Yang, Y. Li, C. Yang, Adv. Energy Mater. 2018, 8, 1800856.\",12.2,,,,,,,PTQ10:IDTPC,,,,,,,,,,,,1.62,,,,75,17.5,,,,,,,930\r\n\"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\",12.8,,,,,,,PTQ10:IDIC-2F,,,,,,,,,,,,1.63,,,,73.6,19.1,,,,,,,910\r\n\"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\",12.9,,,,,,,PTQ10:IDIC,,,,,,,,,,,,1.64,,,,71.3,17.4,,,,,,,960\r\n\"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\",9.3,,,,,,,J51:ITIC,,,,,,,,,,,,1.65,,,,68.7,16.5,,,,,,,820\r\n\"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\",12.1,,,,,,, ,,,,,,,,,,,,1.66,,,,73.2,20.3,,,,,,,815\r\n\"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\",10.2,,,,,,,P4TIF:PC61BM,,,,,,,,,,,,1.67,,,,59.9,21,,,,,,,810\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2016, 24, 3.\",11.5,,,,,,, ,,,,,,,,,,,,1.67,,,,73.7,19.7,,,,,,,791\r\n\"D. Baran, N. Gasparini, A. Wadsworth, C. H. Tan, N. Wehbe, X. Song, Z. Hamid, W. Zhang, M. Neophytou, T. Kirchartz, C. J. Brabec, J. R. Durrant, I. McCulloch, Nat. Commun. 2018, 9, 2059.\",12,,,,,,,PBDTTT-EFT:EHIDTBR,,,,,,,,,,,,1.68,,,,63,18.5,,,,,,,1030\r\n\"C. Li, J. Song, Y. Cai, G. Han, W. Zheng, Y. Yi, H. S. Ryu, H. Y. Woo, Y. Sun, J. Energy Chem. 2020, 40, 144.\",8.9,,,,,,,PBT1-C:NFA,,,,,,,,,,,,1.69,,,,72.9,13.9,,,,,,,878\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\",11.1,,,,,,, ,,,,,,,,,,,,1.7,,,,71.9,17.8,,,,,,,867\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\",10,,,,,,, ,,,,,,,,,,,,1.72,,,,66.4,16.8,,,,,,,899\r\n\"L. Q. Phuong, S. M. Hosseini, C. W. Koh, H. Y. Woo, S. Shoaee, J. Phys. Chem. C 2019, 123, 27417.\",9.6,,,,,,,PPDT2FBT:PC70BM,,,,,,,,,,,,1.78,,,,72,17,,,,,,,786\r\n\"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\",7.5,,,,,,,BDT-ffBX-DT:PDI4,,,,,,,,,,,,1.79,,,,62.1,10.6,,,,,,,1140\r\n\"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\",6.2,,,,,,,BDT-ffBX-DT:SFPDI,,,,,,,,,,,,1.79,,,,56.6,8.9,,,,,,,1230\r\n\"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\",9,,,,,,,BTR:PC71BM,,,,,,,,,,,,1.85,,,,72.9,13.8,,,,,,,900\r\n\"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\",7.6,,,,,,,PBDB-T:PC71BM,,,,,,,,,,,,1.85,,,,69.1,13.3,,,,,,,830\r\n\"M. Li, H. Wang, Y. Liu, Y. Zhou, H. Lu, J. Song, Z. Bo, Dyes Pigm. 2020, 175, 108186.\",7.4,,,,,,,PBDB-T:NDP-Se-DIO,,,,,,,,,,,,1.86,,,,61.9,12.7,,,,,,,940\r\n\"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\",5.7,,,,,,,PBDB-T-2Cl:PC61BM,,,,,,,,,,,,1.88,,,,55.9,10.7,,,,,,,950\r\n\"A. Abdul Raheem, C. Kumar, P. Murugan, C. Praveen, ACS Appl. Energy Mater. 2021, 4, 11609.\",6.3,,,,,,,P3HT:TCBD14,,,,,,,,,,,,1.93,,,,65.3,12.2,,,,,,,790\r\n\"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\",3.7,,,,,,,P3HT:PCBM,,,,,,,,,,,,2.01,,,,59.2,10.4,,,,,,,592\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\",11,,,,,,,,,,,,,,,,,,,1.44,,,,70.3,21.9,,,, ,,,714\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\",11.4,,,,,,,,,,,,,,,,,,,1.52,,,,71.9,21.3,,,, ,,,743\r\n\"T.-K. Chang, Y. Chi, RSC Adv. 2017, 7, 42013.\",10.1,,,,,,,,,,,,,,,,,,,1.59,,,,76.9,18.5,,,,TF-tBu_C3F7,,,710\r\n\"C.-C. Chen, J.-S. Chen, V. S. Nguyen, T.-C. Wei, C.-Y. Yeh, Angew. Chem., Int. Ed. 2021, 60, 4886.\",10.7,,,,,,,,,,,,,,,,,,,1.66,,,,75.9,16.6,,,,bJS2,,,849\r\n\"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\",7.8,,,,,,,,,,,,,,,,,,,1.74,,,,72.7,15.4,,,,YD2,,,694\r\n\"M. Godfroy, J. Liotier, V. M. Mwalukuku, D. Joly, Q. Huaulmé, L. Cabau, C. Aumaitre, Y. Kervella, S. Narbey, F. Oswald, E. Palomares, C. A. González Flores, G. Oskam, R. Demadrille, Sustainable Energy Fuels 2021, 5, 144.\",10.9,,,,,,,,,,,,,,,,,,,1.75,,,,70.8,20.7,,,,YKP-88/YKP-137 (6/4),,,745\r\n\"Z. Ge, C. Wang, Z. Chen, T. Wang, T. Chen, R. Shi, S. Yu, J. Liu, Mater. Res. Bull. 2021, 135, 111148.\",8.3,,,,,,,,,,,,,,,,,,,1.76,,,,66.3,17.9,,,,TNA,,,700\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",10,,,,,,,,,,,,,,,,,,,1.77,,,,74.7,18.1,,,,N719,,,740\r\n\"E. Akman, S. Akin, T. Ozturk, B. Gulveren, S. Sonmezoglu, Sol. Energy 2020, 202, 227.\",9.1,,,,,,,,,,,,,,,,,,,1.8,,,,64,19,,,,N719,,,744\r\n\"C. Wang, X. Zhang, D. Cao, H. Yin, X. Li, P. Cheng, B. Mi, Z. Gao, W. Deng, Org. Electron. 2017, 49, 135.\",9,,,,,,,,,,,,,,,,,,,1.8,,,,57.2,19.8,,,,N719,,,790\r\n\"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\",6.5,,,,,,,,,,,,,,,,,,,1.8,,,,74.5,13.3,,,,SK7,,,663\r\n\"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\",6.4,,,,,,,,,,,,,,,,,,,1.82,,,,71.8,13.1,,,,AN-11,,,680\r\n\"D. Cao, X. Li, X. Yu, N. Cheng, P. Yang, B. Mi, Z. Gao, Phys. Status Solidi A 2020, 217, 1900724.\",8.9,,,,,,,,,,,,,,,,,,,1.83,,,,57.5,19,,,,N719,,,820\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\",12.3,,,,,,,,,,,,,,,,,,,1.85,,,,79.1,15.2,,,, ,,,1020\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",8.3,,,,,,,,,,,,,,,,,,,1.86,,,,71.7,14.8,,,,N719,,,782\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321.\",9.1,,,,,,,,,,,,,,,,,,,1.87,,,,76.7,11.2,,,,L351,,,1060\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",7.8,,,,,,,,,,,,,,,,,,,1.88,,,,74.7,14.3,,,,TY4,,,730\r\n\"X. Wang, A. Bolag, W. Yun, Y. Du, C. Eerdun, X. Zhang, T. Bao, J. Ning, H. Alata, T. Ojiyed, J. Mol. Struct. 2020, 1206, 127694.\",8.5,,,,,,,,,,,,,,,,,,,1.89,,,,68.8,21.3,,,,N719+W2,,,580\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321.\",11.2,,,,,,,,,,,,,,,,,,,1.93,,,,75.6,13,,,,L350,,,1140\r\n\"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\",3,,,,,,,,,,,,,,,,,,,1.97,,,,79.4,6.3,,,,AN-14,,,600\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",5.4,,,,,,,,,,,,,,,,,,,1.99,,,,69.5,11.3,,,,SK6,,,689\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",6.3,,,,,,,,,,,,,,,,,,,2,,,,71.7,12,,,,CW10+SK6,,,732\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321.\",9.2,,,,,,,,,,,,,,,,,,,2.01,,,,72.1,11,,,,L349,,,1160\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",8.1,,,,,,,,,,,,,,,,,,,2.02,,,,75,14.3,,,,TY6,,,760\r\n\"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\",3.9,,,,,,,,,,,,,,,,,,,2.05,,,,77.5,7.4,,,,AN-12,,,680\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",6.9,,,,,,,,,,,,,,,,,,,2.09,,,,76.3,11.6,,,,TY3,,,780\r\n\"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\",5.8,,,,,,,,,,,,,,,,,,,2.12,,,,72.7,10.8,,,,CW10,,,739\r\n\"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\",5.8,,,,,,,,,,,,,,,,,,,2.23,,,,74.8,10.2,,,,MS3,,,760\r\n\"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. Péchy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Grätzel, Angew. Chem. 2018, 130, 14321.\",5.3,,,,,,,,,,,,,,,,,,,2.32,,,,70.8,6.4,,,,L348,,,1170\r\n\"R. Sun, D. Zhuang, M. Zhao, Q. Gong, M. Scarpulla, Y. Wei, G. Ren, Y. Wu, Sol. Energy Mater. Sol. Cells 2018, 174, 494.\",11.2,,,,,,,,,\"Cu2ZnSn(Se,S)4\",,,,,,,,,,0.98,,,,66.8,39.2,,,,,,,430\r\n\"J. Li, J. Huang, K. Li, Y. Zeng, Y. Zhang, K. Sun, C. Yan, C. Xue, C. Chen, T. Chen, M. A. Green, J. Tang, X. Hao, Sol. RRL 2021, 5, 2000693.\",11.6,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.02,,,,67.4,39.2,,,,,,,441\r\n\"Y. S. Lee, T. Gershon, O. Gunawan, T. K. Todorov, T. Gokmen, Y. Virgus, S. Guha, Adv. Energy Mater. 2015, 5, 1401372.\",11.6,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.03,,,,67.3,40.6,,,,,,,423\r\n\"H. Tampo, K. M. Kim, S. Kim, H. Shibata, S. Niki, J. Appl. Phys. 2017, 122, 023106.\",9.6,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.04,,,,64.5,34.9,,,,,,,425\r\n\"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcobé, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. Pérez-Rodríguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\",9.4,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.05,,,,63.3,32.5,,,,,,,457\r\n\"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcobé, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. Pérez-Rodríguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\",9.5,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.06,,,,66.4,31.1,,,,,,,460\r\n\"J. Zhou, X. Xu, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Nano Energy 2021, 89, 106405.\",13.2,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.06,,,,69,40.1,,,,,,,477\r\n\"J. Zhou, X. Xu, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Nano Energy 2021, 89, 106405.\",11.5,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.06,,,,68.2,36.7,,,,,,,461\r\n\"J. Li, Y. Huang, J. Huang, G. Liang, Y. Zhang, G. Rey, F. Guo, Z. Su, H. Zhu, L. Cai, K. Sun, Y. Sun, F. Liu, S. Chen, X. Hao, Y. Mai, M. A. Green, Adv. Mater. 2020, 32, 2005268.\",12.5,,,,,,,,,Cu2ZnSnSe4,,,,,,,,,,1.07,,,,68.2,37.4,,,,,,,491\r\n\"Y. Gong, Y. Zhang, E. Jedlicka, R. Giridharagopal, J. A. Clark, W. Yan, C. Niu, R. Qiu, J. Jiang, S. Yu, S. Wu, H. W. Hillhouse, D. S. Ginger, W. Huang, H. Xin, Sci. China Mater. 2021, 64, 52.\",12.4,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.08,,,,71.3,33.3,,,,,,,522\r\n\"Y. Gong, Y. Zhang, E. Jedlicka, R. Giridharagopal, J. A. Clark, W. Yan, C. Niu, R. Qiu, J. Jiang, S. Yu, S. Wu, H. W. Hillhouse, D. S. Ginger, W. Huang, H. Xin, Sci. China Mater. 2021, 64, 52.\",12.2,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.09,,,,68.8,37.2,,,,,,,475\r\n\"Y. Gong, R. Qiu, C. Niu, J. Fu, E. Jedlicka, R. Giridharagopal, Q. Zhu, Y. Zhou, W. Yan, S. Yu, J. Jiang, S. Wu, D. S. Ginger, W. Huang, H. Xin, Adv. Funct. Mater. 2021, 31, 2101927.\",12.5,,,,,,,,,\"(Ag,Cu)2ZnSn(S,Se)4\",,,,,,,,,,1.09,,,,72.1,32.1,,,,,,,540\r\n\"J. Lee, T. Enkhbat, G. Han, M. H. Sharif, E. Enkhbayar, H. Yoo, J. H. Kim, S. Kim, J. Kim, Nano Energy 2020, 78, 105206.\",11.2,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.1,,,,69.3,36.4,,,,,,,445\r\n\"Y. Gong, Y. Zhang, E. Jedlicka, R. Giridharagopal, J. A. Clark, W. Yan, C. Niu, R. Qiu, J. Jiang, S. Yu, S. Wu, H. W. Hillhouse, D. S. Ginger, W. Huang, H. Xin, Sci. China Mater. 2021, 64, 52.\",11.6,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.11,,,,69.4,32,,,,,,,520\r\n\"S. Kim, K. M. Kim, H. Tampo, H. Shibata, S. Niki, Appl. Phys. Express 2016, 9, 102301.\",12.3,,,,,,,,,Cu2Zn(Sn0.78Ge0.22)Se4,,,,,,,,,,1.12,,,,72.3,32.3,,,,,,,527\r\n\"W. Wang, M. T. Winkler, O. Gunawan, T. Gokmen, T. K. Todorov, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2014, 4, 1301465.\",12.6,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.13,,,,69.8,35.2,,,,,,,513\r\n\"T. K. Todorov, J. Tang, S. Bag, O. Gunawan, T. Gokmen, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2013, 3, 34.\",11.1,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.13,,,,69.8,34.5,,,,,,,460\r\n\"D.-H. Son, S.-H. Kim, S.-Y. Kim, Y.-I. Kim, J.-H. Sim, S.-N. Park, D.-H. Jeon, D.-K. Hwang, S.-J. Sung, J.-K. Kang, K.-J. Yang, D.-H. Kim, J. Mater. Chem. A 2019, 7, 25279.\",12.6,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.14,,,,65.9,35.4,,,,,,,541\r\n\"K.-J. Yang, S. Kim, S.-Y. Kim, D.-H. Son, J. Lee, Y.-I. Kim, S.-J. Sung, D.-H. Kim, T. Enkhbat, J. Kim, J. Kim, W. Jo, J.-K. Kang, Adv. Funct. Mater. 2021, n/a, 2102238.\",11.2,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.16,,,,62.8,33.1,,,,,,,539\r\n\"K. Shen, Y. Zhang, X. Wang, C. Ou, F. Guo, H. Zhu, C. Liu, Y. Gao, R. E. I. Schropp, Z. Li, X. Liu, Y. Mai, Adv. Sci. 2020, n/a, 2001013.\",7.5,,,,,,,,,Sb2Se3,,,,,,,,,,1.22,,,,62.4,28.9,,,,,,,413\r\n\"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\",9.2,,,,,,,,,Sb2Se3,,,,,,,,,,1.24,,,,70.6,32.6,,,,,,,400\r\n\"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\",4.8,,,,,,,,,Sb2Se3,,,,,,,,,,1.27,,,,47.3,27.3,,,,,,,370\r\n\"S. Wen, X. Yin, C. Zhang, Y. Guo, J. Liu, E. Wang, C. Zheng, W. Que, H. Liu, W. Liu, Mater. Lett. 2021, 283, 128770.\",4,,,,,,,,,Sb2Se3,,,,,,,,,,1.29,,,,51,22.9,,,,,,,340\r\n\"K. Li, F. Li, C. Chen, P. Jiang, S. Lu, S. Wang, Y. Lu, G. Tu, J. Guo, L. Shui, Z. Liu, B. Song, J. Tang, Nano Energy 2021, 86, 106101.\",7.3,,,,,,,,,Sb2Se3,,,,,,,,,,1.31,,,,59.7,29.2,,,,,,,420\r\n\"J. Li, J. Huang, K. Li, Y. Zeng, Y. Zhang, K. Sun, C. Yan, C. Xue, C. Chen, T. Chen, M. A. Green, J. Tang, X. Hao, Sol. RRL 2021, 5, 2000693.\",6.4,,,,,,,,,Sb2Se3,,,,,,,,,,1.33,,,,54.7,27.8,,,,,,,421\r\n\"L. Choubrac, M. Bär, X. Kozina, R. Félix, R. G. Wilks, G. Brammertz, S. Levcenko, L. Arzel, N. Barreau, S. Harel, M. Meuris, B. Vermang, ACS Appl. Energy Mater. 2020, 3, 5830.\",8.5,,,,,,,,,Cu2ZnGeSe4,,,,,,,,,,1.45,,,,55.7,24.4,,,,,,,625\r\n\"C. Yan, J. Huang, K. Sun, S. Johnston, Y. Zhang, H. Sun, A. Pu, M. He, F. Liu, K. Eder, L. Yang, J. M. Cairney, N. J. Ekins-Daukes, Z. Hameiri, J. A. Stride, S. Chen, M. A. Green, X. Hao, Nat. Energy 2018, 3, 764.\",11,,,,,,,,,Cu2ZnSnS4,,,,,,,,,,1.5,,,,69.3,21.7,,,,,,,731\r\n\"R. Tang, X. Wang, W. Lian, J. Huang, Q. Wei, M. Huang, Y. Yin, C. Jiang, S. Yang, G. Xing, S. Chen, C. Zhu, X. Hao, M. A. Green, T. Chen, Nat. Energy 2020, 5, 587.\",10,,,,,,,,,\"Sb2(S,Se)3\",,,,,,,,,,1.5,,,,63.3,24.1,,,,,,,655\r\n\"K. Timmo, M. Altosaar, M. Pilvet, V. Mikli, M. Grossberg, M. Danilson, T. Raadik, R. Josepson, J. Krustok, M. Kauk-Kuusik, J. Mater. Chem. A 2019, 7, 24281.\",8.73,,,,,,,,,(Cu0.99Ag0.01)1.85(Zn0.8Cd0.2)1.1SnS4,,,,,,,,,,1.52,,,,63.9,20.6,,,,,,,664\r\n\"R. Nie, M. Hu, A. M. Risqi, Z. Li, S. I. Seok, Adv. Sci. 2021, 8, 2003172.\",4.1,,,,,,,,,SbSeI:Sb2Se3,,,,,,,,,,1.53,,,,58.7,14.8,,,,,,,473\r\n\"Y. C. Choi, D. U. Lee, J. H. Noh, E. K. Kim, S. I. Seok, Adv. Funct. Mater. 2014, 24, 3587.\",7.5,,,,,,,,,Sb2S3,,,,,,,,,,1.8,,,,65,16.1,,,,,,,711\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2014, 22, 1.\",19.8,,,,,,,,,CIGS,,,,,,,,,,1.09,,,,79.2,34.9,,,,,,,716\r\n\"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\",21.7,,,,,,,,,CIGS,,,,,,,,,,1.1,,,,74.3,40.7,,,,,,,718\r\n\"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\",26.7,,,,,,,,,Si (crystalline),,,,,,,,,,1.11,,,,84.9,42.7,,,,,,,738\r\n\"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2018, 26, 427.\",22.9,,,,,,,,,CIGS,,,,,,,,,,1.13,,,,79.5,38.8,,,,,,,744\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 805.\",21,,,,,,,,,CIGS,,,,,,,,,,1.14,,,,77.6,35.7,,,,,,,757\r\n\"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\",23.4,,,,,,,,,CIGS,,,,,,,,,,1.15,,,,80.4,39.6,,,,,,,734\r\n\"W. Li, S. Xu, Y. Dai, P. Ma, Y. Feng, W. Li, H. Luo, C. Yang, Mater. Lett. 2019, 244, 43.\",16.3,,,,,,,,,CIGS,,,,,,,,,,1.3,,,,68.1,31.4,,,,,,,762\r\n\"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics Res. Appl. 2019, 27, 3.\",29.1,,,,,,,,,GaAs,,,,,,,,,,1.42,,,,86.7,29.8,,,,,,,1127\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\",21,,,,,,,,,CdTe,,,,,,,,,,1.42,,,,79.4,30.3,,,,,,,876\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\",18.3,,,,,,,,,CdTe,,,,,,,,,,1.48,,,,77,27,,,,,,,857\r\n\"S. Shukla, M. Sood, D. Adeleye, S. Peedle, G. Kusch, D. Dahliah, M. Melchiorre, G.-M. Rignanese, G. Hautier, R. Oliver, S. Siebentritt, Joule 2021, 5, 1816.\",15.2,,,,,,,,,CIGS,,,,,,,,,,1.6,,,,73,23.1,,,,,,,902\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\",10.2,,,,,,,,,Si (amorphous),,,,,,,,,,1.6,,,,69.8,16.4,,,,,,,896\r\n\"T. Matsui, A. Bidiville, K. Maejima, H. Sai, T. Koida, T. Suezaki, M. Matsumoto, K. Saito, I. Yoshida, M. Kondo, Appl. Phys. Lett. 2015, 106, 053901.\",10.6,,,,,,,,,Si (amorphous),,,,,,,,,,1.69,,,,75.6,16.1,,,,,,,896\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, Prog. Photovoltaics 2010, 18, 346.\",10.1,,,,,,,,,Si (amorphous),,,,,,,,,,1.85,,,,67,16.8,,,,,,,886\r\n\"F. Sahli, J. Werner, B. A. Kamino, M. Bräuninger, R. Monnard, B. Paviet-Salomon, L. Barraud, L. Ding, J. J. Diaz Leon, D. Sacchetto, G. Cattaneo, M. Despeisse, M. Boccard, S. Nicolay, Q. Jeangros, B. Niesen, C. Ballif, Nat. Mater. 2018, 17, 820.\",24.1,,,,,,,,,,,,,,Si,,,,,,1.63,1.11,,69.1,19.5,,,,,,\"CsxFA1−xPb(I,Br)3\",1786\r\n\"B. Chen, Z. J. Yu, S. Manzoor, S. Wang, W. Weigand, Z. Yu, G. Yang, Z. Ni, X. Dai, Z. C. Holman, J. Huang, Joule 2020, 4, 850.\",26,,,,,,,,,,,,,,Si,,,,,,1.66,1.11,,75.4,19.2,,,,,,Cs0.1MA0.9PbI2.7Br0.3,1820\r\n\"D. Kim, H. J. Jung, I. J. Park, B. W. Larson, S. P. Dunfield, C. Xiao, J. Kim, J. Tong, P. Boonmongkolras, S. G. Ji, F. Zhang, S. R. Pae, M. Kim, S. B. Kang, V. Dravid, J. J. Berry, J. Y. Kim, K. Zhu, D. H. Kim, B. Shin, Science 2020, 368, 155.\",26.7,,,,,,,,,,,,,,Si,,,,,,1.67,1.11,,79.2,19.2,,,,,,PEA(I0.25SCN0.75),1756\r\n\"Y. Hou, E. Aydin, M. De Bastiani, C. Xiao, F. H. Isikgor, D.-J. Xue, B. Chen, H. Chen, B. Bahrami, A. H. Chowdhury, A. Johnston, S.-W. Baek, Z. Huang, M. Wei, Y. Dong, J. Troughton, R. Jalmood, A. J. Mirabelli, T. G. Allen, E. Van Kerschaver, M. I. Saidaminov, D. Baran, Q. Qiao, K. Zhu, S. De Wolf, E. H. Sargent, Science 2020, 367, 1135.\",25.7,,,,,,,,,,,,,,Si,,,,,,1.68,1.11,,75.4,19.1,,,,,,Cs0.05MA0.15FA0.8PbI2.25Br0.75,1781\r\n\"M. De Bastiani, A. J. Mirabelli, Y. Hou, F. Gota, E. Aydin, T. G. Allen, J. Troughton, A. S. Subbiah, F. H. Isikgor, J. Liu, L. Xu, B. Chen, E. Van Kerschaver, D. Baran, B. Fraboni, M. F. Salvador, U. W. Paetzold, E. H. Sargent, S. De Wolf, Nat. Energy 2021, 6, 167.\",25.2,,,,,,,,,,,,,,Si,,,,,,1.68,1.11,,75.6,18.4,,,,,, ,1800\r\n\"E. Köhnen, M. Jošt, A. B. Morales-Vilches, P. Tockhorn, A. Al-Ashouri, B. Macco, L. Kegelmann, L. Korte, B. Rech, R. Schlatmann, B. Stannowski, S. Albrecht, Sustainable Energy Fuels 2019, 3, 1995.\",26,,,,,,,,,,,,,,Si,,,,,,1.64,1.12,,76.5,19.2,,,,,,FA0.83MA0.17PbI3,1760\r\n\"M. Jošt, E. Köhnen, A. B. Morales-Vilches, B. Lipovšek, K. Jäger, B. Macco, A. Al-Ashouri, J. Krč, L. Korte, B. Rech, R. Schlatmann, M. Topič, B. Stannowski, S. Albrecht, Energy Environ. Sci. 2018, 11, 3511.\",26.5,,,,,,,,,,,,,,Si,,,,,,1.65,1.12,,77,19.4,,,,,,Cs0.05MA0.16FA0.79PbI2.49Br0.51,1760\r\n\"A. Al-Ashouri, E. Köhnen, B. Li, A. Magomedov, H. Hempel, P. Caprioglio, J. A. Márquez, A. B. Morales Vilches, E. Kasparavicius, J. A. Smith, N. Phung, D. Menzel, M. Grischek, L. Kegelmann, D. Skroblin, C. Gollwitzer, T. Malinauskas, M. Jošt, G. Matič, B. Rech, R. Schlatmann, M. Topič, L. Korte, A. Abate, B. Stannowski, D. Neher, M. Stolterfoht, T. Unold, V. Getautis, S. Albrecht, Science 2020, 370, 1300.\",28.8,,,,,,,,,,,,,,Si,,,,,,1.68,1.12,,78.9,19.2,,,,,,Cs0.05FA0.73MA0.22PbI2.31Br0.69,1895\r\n\"G. Nogay, F. Sahli, J. Werner, R. Monnard, M. Boccard, M. Despeisse, F. J. Haug, Q. Jeangros, A. Ingenito, C. Ballif, ACS Energy Lett. 2019, 4, 844.\",24.9,,,,,,,,,,,,,,Si,,,,,,1.65,1.13,,73.5,19.5,,,,,,CsFAPb(IBr)3,1735\r\n\"J. Xu, C. C. Boyd, Z. J. Yu, A. F. Palmstrom, D. J. Witter, B. W. Larson, R. M. France, J. Werner, S. P. Harvey, E. J. Wolf, W. Weigand, S. Manzoor, M. F. A. M. van Hest, J. J. Berry, J. M. Luther, Z. C. Holman, M. D. McGehee, Science 2020, 367, 1097.\",27.1,,,,,,,,,,,,,,Si,,,,,,1.67,1.13,,75.3,19.1,,,,,,CsFAMAPb(IBrCl)3,1886\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics Res. Appl. 2021, 29, 657.\",29.5,,,,,,,,,,,,,,Si,,,,,,1.69,1.13,,77.3,20.3,,,,,, ,1884\r\n\"J. Werner, C.-H. Weng, A. Walter, L. Fesquet, J. P. Seif, S. De Wolf, B. Niesen, C. Ballif, J. Phys. Chem. Lett. 2016, 7, 161.\",20.9,,,,,,,,,,,,,,Si,,,,,,1.62,1.15,,77.6,15.9,,,,,,MAPI,1690\r\n\"B. Chen, Z. Yu, K. Liu, X. Zheng, Y. Liu, J. Shi, D. Spronk, P. N. Rudd, Z. Holman, J. Huang, Joule 2019, 3, 177.\",25.4,,,,,,,,,,,,,,Si,,,,,,1.68,1.15,,79.4,17.8,,,,,,Cs0.15FA0.71MA0.14PbI2.4Br0.6,1800\r\n\"K. A. Bush, S. Manzoor, K. Frohna, Z. J. Yu, J. A. Raiford, A. F. Palmstrom, H.-P. Wang, R. Prasanna, S. F. Bent, Z. C. Holman, M. D. McGehee, ACS Energy Lett. 2018, 3, 2173.\",25,,,,,,,,,,,,,,Si,,,,,,1.68,1.15,,77,18.4,,,,,,FA0.75Cs0.25PbI2.4Br0.6,1770\r\n\"J. Werner, C.-H. Weng, A. Walter, L. Fesquet, J. P. Seif, S. De Wolf, B. Niesen, C. Ballif, J. Phys. Chem. Lett. 2016, 7, 161.\",19.2,,,,,,,,,,,,,,Si,,,,,,1.62,1.16,,70.1,16.1,,,,,,MAPI,1701\r\n\"Z. Li, T. H. Kim, S. Y. Han, Y.-J. Yun, S. Jeong, B. Jo, S. A. Ok, W. Yim, S. H. Lee, K. Kim, S. Moon, J.-Y. Park, T. K. Ahn, H. Shin, J. Lee, H. J. Park, Adv. Energy Mater. 2020, 10, 1903085.\",24.3,,,,,,,,,,,,,,GaAs,,,,,,1.85,1.42,,78.8,14.3,,,,,,FA0.80MA0.04Cs0.16Pb(I0.50Br0.50)3,2160\r\n\"Q. Han, Y.-T. Hsieh, L. Meng, J.-L. Wu, P. Sun, E.-P. Yao, S.-Y. Chang, S.-H. Bae, T. Kato, V. Bermudez, Y. Yang, Science 2018, 361, 904.\",22.4,,,,,,,,,,,,,,CIGS,,,,,,1.65,1.1,,73.1,17.3,,,,,,Cs0.09FA0.77MA0.14Pb(I0.86Br0.14)3,1774\r\n\"M. Jošt, T. Bertram, D. Koushik, J. A. Marquez, M. A. Verheijen, M. D. Heinemann, E. Köhnen, A. Al-Ashouri, S. Braunger, F. Lang, B. Rech, T. Unold, M. Creatore, I. Lauermann, C. A. Kaufmann, R. Schlatmann, S. Albrecht, ACS Energy Lett. 2019, 4, 583.\",21.6,,,,,,,,,,,,,,CIGS,,,,,,1.64,1.11,,76,18,,,,,,Cs0.05(MA0.17FA0.83)Pb1.1(I0.83Br0.17)3,1580\r\n\"A. Al-Ashouri, A. Magomedov, M. Roß, M. Jošt, M. Talaikis, G. Chistiakova, T. Bertram, J. A. Márquez, E. Köhnen, E. Kasparavičius, S. Levcenco, L. Gil-Escrig, C. J. Hages, R. Schlatmann, B. Rech, T. Malinauskas, T. Unold, C. A. Kaufmann, L. Korte, G. Niaura, V. Getautis, S. Albrecht, Energy Environ. Sci. 2019, 12, 3356.\",23.3,,,,,,,,,,,,,,CIGS,,,,,,1.65,1.11,,71.9,19.2,,,,,,Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3,1680\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2020, 28, 629.\",24.2,,,,,,,,,,,,,,CIGS,,,,,,1.68,1.12,,72.9,19.2,,,,,, ,1768\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics Res. Appl. 2021, 29, 657.\",26.4,,,,,,,,,,,,,, ,,,,,,1.81,1.26,,77.9,16.5,,,,,, ,2048\r\n\"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\",24,,,,,,,,,,,,,,FSA:MA0.3FA0.7Pb0.5Sn0.5I3,,,,,,1.82,1.26,,76.6,15.8,,,,,,FA0.8Cs0.2Pb(I0.6Br0.4)3,1986\r\n\"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\",25.5,,,,,,,,,,,,,,FSA:MA0.3FA0.7Pb0.5Sn0.5I3,,,,,,1.82,1.26,,79.8,15.9,,,,,,FA0.8Cs0.2Pb(I0.6Br0.4)3,2009\r\n\"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\",22.9,,,,,,,,,,,,,,(FASnI3)0.6(MAPbI3)0.4,,,,,,1.72,1.27,,79.8,15,,,,,,Cs0.05FA0.8MA0.15PbI2.55Br0.45,1915\r\n\"Z. Yu, Z. Yang, Z. Ni, Y. Shao, B. Chen, Y. Lin, H. Wei, Z. J. Yu, Z. Holman, J. Huang, Nat. Energy 2020, 5, 657.\",24.3,,,,,,,,,,,,,,Cs0.05MA0.45FA0.5Pb0.5Sn0.5I3,,,,,,1.81,1.27,,78.8,15.2,,,,,,Cs0.4FA0.6PbI1.95Br1.05,2030\r\n\"R. Lin, K. Xiao, Z. Qin, Q. Han, C. Zhang, M. Wei, M. I. Saidaminov, Y. Gao, J. Xu, M. Xiao, A. Li, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2019, 4, 864.\",24.5,,,,,,,,,,,,,,FA0.7MA0.3Pb0.5Sn0.5I3,,,,,,1.81,1.27,,80,15.9,,,,,,FA0.8Cs0.2Pb(I0.6Br0.4)3,1927\r\n\"A. F. Palmstrom, G. E. Eperon, T. Leijtens, R. Prasanna, S. N. Habisreutinger, W. Nemeth, E. A. Gaulding, S. P. Dunfield, M. Reese, S. Nanayakkara, T. Moot, J. Werner, J. Liu, B. To, S. T. Christensen, M. D. McGehee, M. F. A. M. van Hest, J. M. Luther, J. J. Berry, D. T. Moore, Joule 2019, 3, 2193.\",23.1,,,,,,,,,,,,,,FA0.75Cs0.25Sn0.5Pb0.5I3,,,,,,1.73,1.28,,77,16,,,,,,FA0.6Cs0.3DMA0.1PbI2.4Br0.6,1880\r\n\"Q. Zeng, L. Liu, Z. Xiao, F. Liu, Y. Hua, Y. Yuan, L. Ding, Sci. Bull. 2019, 64, 885.\",15,,,,,,,,,,,,,,PTB7-Th:COi8DFIC:PC71BM,,,,,,1.91,1.25,,73.4,12,,,,,,CsPbI2Br,1710\r\n\"P. Wang, W. Li, O. J. Sandberg, C. Guo, R. Sun, H. Wang, D. Li, H. Zhang, S. Cheng, D. Liu, J. Min, A. Armin, T. Wang, Nano Lett. 2021, 21, 7845.\",21.1,,,,,,,,,,,,,,PM6:Y6-BO,,,,,,1.91,1.38,,80.9,13.3,,,,,,CsPbI2Br,1960\r\n\"Z. Li, S. Wu, J. Zhang, K. C. Lee, H. Lei, F. Lin, Z. Wang, Z. Zhu, A. K. Y. Jen, Adv. Energy Mater. 2020, 10, 2000361.\",15.1,,,,,,,,,,,,,,PBDB-T:SN6IC-4F,,,,,,1.83,1.4,,71,11.5,,,,,,Cs0.1(FA0.6MA0.4)0.9Pb(I0.6Br0.4)3,1850\r\n\"X. Chen, Z. Jia, Z. Chen, T. Jiang, L. Bai, F. Tao, J. Chen, X. Chen, T. Liu, X. Xu, C. Yang, W. Shen, W. E. I. Sha, H. Zhu, Y. Yang, Joule 2020, 4, 1594.\",19.5,,,,,,,,,,,,,,PBDBT-2F:Y6:PC71BM,,,,,,1.82,1.4,,77.2,13.1,,,,,,FA0.8MA0.02Cs0.18PbI1.8Br1.2,1925\r\n\"X. Chen, Z. Jia, Z. Chen, T. Jiang, L. Bai, F. Tao, J. Chen, X. Chen, T. Liu, X. Xu, C. Yang, W. Shen, W. E. I. Sha, H. Zhu, Y. Yang, Joule 2020, 4, 1594.\",20.4,,,,,,,,,,,,,,PBDBT-2F:Y6:PC71BM,,,,,,1.82,1.4,,81.5,13.1,,,,,,FA0.8MA0.02Cs0.18PbI1.8Br1.2,1902\r\n\"M. Hosseinnezhad, J. Electron. Mater. 2019, 48, 5403.\",10.5,,,,,,,,,,,,,,(FAPbI3)0.85(MAPbBr3)0.15,,,,,,1.93,1.59,,70,12.9,,,,,,N719,1170\r\n\"Z. Jia, S. Qin, L. Meng, Q. Ma, I. Angunawela, J. Zhang, X. Li, Y. He, W. Lai, N. Li, H. Ade, C. J. Brabec, Y. Li, Nat. Commun. 2021, 12, 178.\",16.4,,,,,,,,,,,,,PTB7-Th:BTPV-4F:PC71BM,,,,,,,1.66,1.23,,68.5,14.5,,,,,PM6:m-DTC-2F,,1650\r\n\"L. Meng, Y. Zhang, X. Wan, C. Li, X. Zhang, Y. Wang, X. Ke, Z. Xiao, L. Ding, R. Xia, H.-L. Yip, Y. Cao, Y. Chen, Science 2018, 361, 1094.\",17.3,,,,,,,,,,,,,PTB7-Th:O6T-4F:PC71BM,,,,,,,1.72,1.24,,73.3,14.4,,,,,PBDB-T:F-M,,1640\r\n\"X. Huang, B. Sun, Y. Li, C. Jiang, D. Fan, J. Fan, S. R. Forrest, Appl. Phys. Lett. 2020, 116, 153501.\",15.9,,,,,,,,,,,,,PM6:SFT8-4F,,,,,,,1.64,1.31,,68,14.1,,,,,PCE-10:BT-CIC:BEIT-4F,,1660\r\n\"G. Liu, J. Jia, K. Zhang, X. e. Jia, Q. Yin, W. Zhong, L. Li, F. Huang, Y. Cao, Adv. Energy Mater. 2019, 9, 1803657.\",15,,,,,,,,,,,,,PTB7-Th:PCDTBT:IEICO-4F,,,,,,,1.65,1.32,,69,13.6,,,,,PBDB-T-2F:TfIF-4FIC,,1600\r\n\"J. Wang, Z. Zheng, Y. Zu, Y. Wang, X. Liu, S. Zhang, M. Zhang, J. Hou, Adv. Mater. 2021, 33, 2102787.\",19.6,,,,,,,,,,,,,PBDB-TF:ITCC,,,,,,,1.74,1.32,,72.4,14.2,,,,,PBDB-TF:BTP-eC11,,1910\r\n\"J. Wang, Z. Zheng, Y. Zu, Y. Wang, X. Liu, S. Zhang, M. Zhang, J. Hou, Adv. Mater. 2021, 33, 2102787.\",19.5,,,,,,,,,,,,,PBDB-TF:ITCC,,,,,,,1.74,1.32,,72,14.2,,,,,PBDB-TF:BTP-eC11,,1912\r\n\"M. M. Tavakoli, H. Si, J. Kong, Energy Technol. 2021, 9, 2000751.\",15.2,,,,,,,,,,,,,PM6:Y6,,,,,,,1.73,1.37,,73,12.9,,,,,PV2000:PCBM,,1610\r\n\"X. Che, Y. Li, Y. Qu, S. R. Forrest, Nat. Energy 2018, 3, 422.\",15,,,,,,,,,,,,,PCE-10:BTCIC,,,,,,,1.79,1.42,,71,13.3,,,,,DTDCPB:C70,,1590\r\n\"Y. Zhang, B. Kan, Y. Sun, Y. Wang, R. Xia, X. Ke, Y.-Q.-Q. Yi, C. Li, H.-L. Yip, X. Wan, Y. Cao, Y. Chen, Adv. Mater. 2018, 30, 1707508.\",14.1,,,,,,,,,,,,,PTB7-Th: NOBDT,,,,,,,1.74,1.48,,70,11.7,,,,,PBDB-T: F-M,,1710\r\n\"J. Troughton, S. Neubert, N. Gasparini, D. R. Villalva, J. Bertrandie, A. Seitkhan, S. H. K. Paleti, A. Sharma, M. De Bastiani, E. Aydin, T. D. Anthopoulos, S. De Wolf, R. Schlatmann, D. Baran, Adv. Energy Mater. 2021, 11, 2100166.\",15.1,,,,,,,,,,,,,PTB7-Th:IEICO-4F,,,,,,,1.78,1.33,,71,13.2,,,,,a-Si,,1610\r\n\"A. B. Nikolskaia, M. F. Vildanova, S. S. Kozlov, O. I. Shevaleevskiy, Semiconductors 2018, 52, 88.\",14.7,,,,,,,,,,,,,Si,,,,,,,1.84,1.11,,62,40.9,,,,,N719,,580\r\n\"J. Kwon, M. J. Im, C. U. Kim, S. H. Won, S. B. Kang, S. H. Kang, I. T. Choi, H. K. Kim, I. H. Kim, J. H. Park, K. J. Choi, Energy Environ. Sci. 2016, 9, 3657.\",17.2,,,,,,,,,,,,,Si,,,,,,,1.67,1.24,,69.3,18.1,,,,,SGT-021,,1360\r\n\"S. H. Moon, S. J. Park, S. H. Kim, M. W. Lee, J. Han, J. Y. Kim, H. Kim, Y. J. Hwang, D.-K. Lee, B. K. Min, Sci. Rep. 2015, 5, 8970.\",13,,,,,,,,,,,,,CIGS,,,,,,,1.82,1.21,,77,14.6,,,,,N719,,1170\r\n\"W.-S. Jeong, J.-W. Lee, S. Jung, J. H. Yun, N.-G. Park, Sol. Energy Mater. Sol. Cells 2011, 95, 3419.\",12.4,,,,,,,,,,,,,CIGS,,,,,,,1.9,1.22,,61,14.1,,,,,N719,,1435\r\n\"P. Liska, K. R. Thampi, M. Grätzel, D. Brémaud, D. Rudmann, H. M. Upadhyaya, A. N. Tiwari, Appl. Phys. Lett. 2006, 88, 203103.\",15.1,,,,,,,,,,,,,CIGS,,,,,,,1.82,1.22,,74,14.1,,,,,N719,,1450\r\n\"T. Kinoshita, J. T. Dy, S. Uchida, T. Kubo, H. Segawa, Nat. Photonics 2013, 7, 535.\",11.4,,,,,,,,,,,,,DX1,,,,,,,1.98,1.4,,66.7,12.2,,,,,N719,,1400\r\n\"T. Yamaguchi, Y. Uchida, S. Agatsuma, H. Arakawa, Sol. Energy Mater. Sol. Cells 2009, 93, 733.\",10.4,,,,,,,,,,,,,N719,,,,,,,1.95,1.44,,67,10.8,,,,,Black dye,,1450\r\n\"A. K. Baranwal, T. Shiki, Y. Ogomi, S. S. Pandey, T. Ma, S. Hayase, RSC Adv. 2014, 4, 47735.\",7.1,,,,,,,,,,,,,N719,,,,,,,2.37,1.78,,69,7.2,,,,,D131,,1420\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2020, 28, 629.\",32.9,,,,,,,,,,,,,GaAs,,,,,,,1.9,1.35,,85.7,15.4,,,,,GaInP,,2500\r\n\"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2018, 26, 3.\",32.8,,,,,,,,,,,,,GaAs,,,,,,,1.88,1.41,,87.7,14.66,,,,,GaInP,,2568\r\n\"T. S. Kim, H. J. Kim, D.-M. Geum, J.-H. Han, I. S. Kim, N. Hong, G. H. Ryu, J. Kang, W. J. Choi, K. J. Yu, ACS Appl. Mater. Interfaces 2021, 13, 13248.\",27.4,,,,,,,,,,,,,GaAs,,,,,,,1.92,1.41,,88,13.1,,,,,GaInP,,2400\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2016, 24, 905.\",31.6,,,,,,,,,,,,,GaAs,,,,,,,1.85,1.42,,87.7,14.2,,,,,GaInP,,2538\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2020, 28, 629.\",23.4,,,,,,,,,,,,,Si,,,,,,,1.9,1.17,,77.7,17.34,,,,,GaAsP,,1732\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2014, 22, 701.\",11.8,,,,,,,,,,,,,nc-Si,,,,,,,1.93,1.36,,67.5,12.27,,,,,a-Si,,1428\r\n\"M. Ma, Q. Tang, H. Chen, B. He, P. Yang, Sol. Energy Mater. Sol. Cells 2017, 160, 67.\",3.6,,,,,,,,,,(5-AVA)y(MA)1−yPbI3,,,,,,,,,1.47,,,,40.6,14.5,,,,,,,616\r\n\"N. Ren, B. Chen, R. Li, P. Wang, S. Mazumdar, B. Shi, C. Zhu, Y. Zhao, X. Zhang, Sol. RRL 2021, 5, 2000795.\",20.2,,,,,,,,,,FA0.87MA0.13PbI3−xClx,,,,,,,,,1.53,,,,72.9,24.7,,,,,,,1123\r\n\"D. Yang, R. Yang, K. Wang, C. Wu, X. Zhu, J. Feng, X. Ren, G. Fang, S. Priya, S. Liu, Nat. Commun. 2018, 9, 3239.\",18.3,,,,,,,,,,FA0.95Cs0.05PbI3,,,,,,,,,1.54,,,,71.5,23.4,,,,,,,1090\r\n\"J. H. Heo, D. H. Shin, D. H. Song, D. H. Kim, S. J. Lee, S. H. Im, J. Mater. Chem. A 2018, 6, 8251.\",18.2,,,,,,,,,,FAPbI3−xBrx,,,,,,,,,1.54,,,,76.9,22.1,,,,,,,1070\r\n\"J. Chung, S. S. Shin, K. Hwang, G. Kim, K. W. Kim, D. S. Lee, W. Kim, B. S. Ma, Y.-K. Kim, T.-S. Kim, J. Seo, Energy Environ. Sci. 2020, 13, 4854.\",20.8,,,,,,,,,,(FAPbI3)0.95(MAPbBr3)0.05,,,,,,,,,1.56,,,,79.6,21.9,,,,,,,1190\r\n\"E. Cho, Y. Y. Kim, D. S. Ham, J. H. Lee, J.-S. Park, J. Seo, S.-J. Lee, Nano Energy 2021, 82, 105737.\",20.3,,,,,,,,,,(FAPbI3)0.95(MAPbBr3)0.05,,,,,,,,,1.56,,,,74.8,23.4,,,,,,,1160\r\n\"L. Yang, Q. Xiong, Y. Li, P. Gao, B. Xu, H. Lin, X. Li, T. Miyasaka, J. Mater. Chem. A 2021, 9, 1574.\",19.9,,,,,,,,,,Cs0.05Rb0.05(FA0.83MA0.17)0.90Pb(I0.95Br0.05)3,,,,,,,,,1.56,,,,77.3,23.2,,,,,,,1109\r\n\"J. Chung, S. S. Shin, K. Hwang, G. Kim, K. W. Kim, D. S. Lee, W. Kim, B. S. Ma, Y.-K. Kim, T.-S. Kim, J. Seo, Energy Environ. Sci. 2020, 13, 4854.\",19.9,,,,,,,,,,(FAPbI3)0.95(MAPbBr3)0.05,,,,,,,,,1.56,,,,76.3,21.9,,,,,,,1192\r\n\"K. Huang, Y. Peng, Y. Gao, J. Shi, H. Li, X. Mo, H. Huang, Y. Gao, L. Ding, J. Yang, Adv. Energy Mater. 2019, 9, 1901419.\",19.5,,,,,,,,,,FA0.945MA0.025Cs0.03Pb(I0.975Br0.025)3,,,,,,,,,1.57,,,,76,23.1,,,,,,,1110\r\n\"S. Zhang, H. Wang, X. Duan, L. Rao, C. Gong, B. Fan, Z. Xing, X. Meng, B. Xie, X. Hu, Adv. Funct. Mater. 2021, n/a, 2106495.\",19.2,,,,,,,,,,Cs0.08MA0.05FA0.87PbI2.88Br0.12,,,,,,,,,1.58,,,,78.9,21.7,,,,,,,1120\r\n\"X. Hu, X. Meng, X. Yang, Z. Huang, Z. Xing, P. Li, L. Tan, M. Su, F. Li, Y. Chen, Y. Song, Sci. Bulletin 2021, 66, 527.\",19.9,,,,,,,,,,FAMAPb(IBr)3,,,,,,,,,1.59,,,,77.5,23,,,,,,,1120\r\n\"X. Dai, Y. Deng, C. H. Van Brackle, S. Chen, P. N. Rudd, X. Xiao, Y. Lin, B. Chen, J. Huang, Adv. Energy Mater. 2020, 10, 1903108.\",19.3,,,,,,,,,,MAPbI3–NH4Cl,,,,,,,,,1.59,,,,78.1,22.7,,,,,,,1090\r\n\"X. Yu, Z. Li, X. Sun, C. Zhong, Z. Zhu, Z. a. Li, A. K. Y. Jen, Nano Energy 2021, 82, 105701.\",17.2,,,,,,,,,,(FA0.92MA0.08)0.9Cs0.1Pb(I0.92Br0.08)3,,,,,,,,,1.59,,,,75,21.42,,,,,,,1070\r\n\"Z. Wang, L. Zeng, C. Zhang, Y. Lu, S. Qiu, C. Wang, C. Liu, L. Pan, S. Wu, J. Hu, G. Liang, P. Fan, H.-J. Egelhaaf, C. J. Brabec, F. Guo, Y. Mai, Adv. Funct. Mater. 2020, 30, 2001240.\",19,,,,,,,,,,MAPbI3,,,,,,,,,1.6,,,,80,21.8,,,,,,,1090\r\n\"J. Feng, X. Zhu, Z. Yang, X. Zhang, J. Niu, Z. Wang, S. Zuo, S. Priya, S. Liu, D. Yang, Adv. Mater. 2018, 30, 1801418.\",18.4,,,,,,,,,,MAPbI3–dimethylsulfide,,,,,,,,,1.6,,,,74.2,22.5,,,,,,,1103\r\n\"C. Liu, J. Sun, X.-F. Jiang, L. Huang, Q. Lou, Y.-B. Cheng, S. Song, Z. Ge, Sci. China Chem. 2021, 64, 281.\",18.3,,,,,,,,,,Cs0.05FA0.79MA0.16PbI2.49Br0.51,,,,,,,,,1.6,,,,75.6,22.4,,,,,,,1080\r\n\"C. Liu, L. Zhang, X. Zhou, J. Gao, W. Chen, X. Wang, B. Xu, Adv. Funct. Mater. 2019, 29, 1807604.\",17.3,,,,,,,,,,Cs0.05FA0.81MA0.14PbI2.55Br0.45,,,,,,,,,1.61,,,,74.9,21.7,,,,,,,1062\r\n\"M. M. Tavakoli, P. Yadav, D. Prochowicz, R. Tavakoli, Sol. RRL 2021, 5, 2000552.\",18.5,,,,,,,,,,MAPbI3,,,,,,,,,1.61,,,,74.3,22.7,,,,,,,1100\r\n\"B. Cao, L. Yang, S. Jiang, H. Lin, N. Wang, X. Li, J. Mater. Chem. A 2019, 7, 4960.\",19.1,,,,,,,,,,Rb0.01K0.04 (Cs0.05(FA0.83MA0.17)0.95)0.95Pb(I0.83Br0.17)3,,,,,,,,,1.61,,,,79.2,21.2,,,,,,,1135\r\n\"Q. Dong, C. Zhu, M. Chen, C. Jiang, J. Guo, Y. Feng, Z. Dai, S. K. Yadavalli, M. Hu, X. Cao, Y. Li, Y. Huang, Z. Liu, Y. Shi, L. Wang, N. P. Padture, Y. Zhou, Nat. Commun. 2021, 12, 973.\",20.1,,,,,,,,,,Cs0.04(FA0.84MA0.16)0.96Pb(I0.84Br0.16)3,,,,,,,,,1.62,,,,78,22.4,,,,,,,1150\r\n\"D. Xin, S. Tie, X. Zheng, J. Zhu, W.-H. Zhang, J. Energy Chem. 2020, 46, 173.\",18,,,,,,,,,,Cs0.06FA0.79MA0.15PbI2.55Br0.45,,,,,,,,,1.62,,,,72.1,22.3,,,,,,,1120\r\n\"M. Gao, X. Han, X. Zhan, P. Liu, Y. Shan, Y. Chen, J. Li, R. Zhang, S. Wang, Q. Zhang, Y. Zheng, L. Chen, Mater. Lett. 2019, 248, 16.\",10.4,,,,,,,,,,(FAPbI3)0.85(MAPbBr3)0.15,,,,,,,,,1.63,,,,52.8,19.2,,,,,,,1030\r\n\"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\",11.2,,,,,,,,,,MAPbI3,,,,,,,,,1.65,,,,64.9,18.4,,,,,,,940\r\n\"J. Xi, Z. Wu, K. Xi, H. Dong, B. Xia, T. Lei, F. Yuan, W. Wu, B. Jiao, X. Hou, Nano Energy 2016, 26, 438.\",7.9,,,,,,,,,,(α-FAPbI3)0.5(MAPbI2Br)0.5,,,,,,,,,1.65,,,,70.7,10.8,,,,,,,1090\r\n\"J. W. Kim, D. Yuk, W. Lee, S. Rasool, J. Y. Kim, ECS J. Solid State Sci. Technol. 2021, 10, 065007.\",7.4,,,,,,,PTB7-Th:COi 8DFIC:PC71BM,,,,,,,,,,,,1.27,,,,65.2,15.9,,,,,,,708\r\n\"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\",10.6,,,,,,,PTB7-Th:IEICO-4F,,,,,,,,,,,,1.32,,,,63.2,24.3,,,,,,,690\r\n\"T.-Y. Qu, L.-J. Zuo, J.-D. Chen, X. Shi, T. Zhang, L. Li, K.-C. Shen, H. Ren, S. Wang, F.-M. Xie, Y.-Q. Li, A. K. Y. Jen, J.-X. Tang, Adv. Opt. Mater. 2020, 8, 2000669.\",16.1,,,,,,,PM6:N3:PC71BM,,,,,,,,,,,,1.37,,,,76.7,25,,,,,,,840\r\n\"Z. Wang, Y. Han, L. Yan, C. Gong, J. Kang, H. Zhang, X. Sun, L. Zhang, J. Lin, Q. Luo, C.-Q. Ma, Adv. Funct. Mater. 2021, 31, 2007276.\",14.4,,,,,,,PM6:Y6,,,,,,,,,,,,1.38,,,,73.2,23.5,,,,,,,837\r\n\"F. Qin, L. Sun, H. Chen, Y. Liu, X. Lu, W. Wang, T. Liu, X. Dong, P. Jiang, Y. Jiang, L. Wang, Y. Zhou, Adv. Mater. 2021, n/a, 2103017.\",16.1,,,,,,,PBDB-T-2F:BTP-eC9:PC71BM,,,,,,,,,,,,1.39,,,,75.8,25.9,,,,,,,820\r\n\"J. Wan, Y. Xia, J. Fang, Z. Zhang, B. Xu, J. Wang, L. Ai, W. Song, K. N. Hui, X. Fan, Y. Li, Nano-Micro Lett. 2021, 13, 44.\",16.1,,,,,,,PM6:Y6,,,,,,,,,,,,1.4,,,,74.7,25.9,,,,,,,860\r\n\"X. Chen, G. Xu, G. Zeng, H. Gu, H. Chen, H. Xu, H. Yao, Y. Li, J. Hou, Y. Li, Adv. Mater. 2020, 32, 1908478.\",15.2,,,,,,,PBDB-T-2F:Y6,,,,,,,,,,,,1.4,,,,73,25.1,,,,,,,832\r\n\"T. Yan, W. Song, J. Huang, R. Peng, L. Huang, Z. Ge, Adv. Mater. 2019, 31, 1902210.\",14.1,,,,,,,PM6:Y6:PC71BM,,,,,,,,,,,,1.4,,,,72,23.6,,,,,,,828\r\n\"W. Song, Y. Liu, B. Fanady, Y. Han, L. Xie, Z. Chen, K. Yu, X. Peng, X. Zhang, Z. Ge, Nano Energy 2021, 86, 106044.\",15.1,,,,,,,PM6:Y6:C6,,,,,,,,,,,,1.41,,,,71.6,24.9,,,,,,,847\r\n\"J. Wan, Y. Xia, J. Fang, Z. Zhang, B. Xu, J. Wang, L. Ai, W. Song, K. N. Hui, X. Fan, Y. Li, Nano-Micro Lett. 2021, 13, 44.\",16.6,,,,,,,PM6:Y6,,,,,,,,,,,,1.42,,,,74.7,25.9,,,,,,,860\r\n\"J. W. Kim, D. Yuk, W. Lee, S. Rasool, J. Y. Kim, ECS J. Solid State Sci. Technol. 2021, 10, 065007.\",10.4,,,,,,,PM6:Y6,,,,,,,,,,,,1.44,,,,72.2,17,,,,,,,848\r\n\"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\",12,,,,,,,PM6:IT-4F,,,,,,,,,,,,1.55,,,,73.3,19.5,,,,,,,840\r\n\"X. Dong, P. Shi, L. Sun, J. Li, F. Qin, S. Xiong, T. Liu, X. Jiang, Y. Zhou, J. Mater. Chem. A 2019, 7, 1989.\",11.6,,,,,,,PBDB-T-2F:IT-4F,,,,,,,,,,,,1.56,,,,72.2,19.6,,,,,,,820\r\n\"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\",12.1,,,,,,,PBDB-T-2F:IT-4F,,,,,,,,,,,,1.56,,,,70.1,20.9,,,,,,,826\r\n\"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\",10.9,,,,,,,PBDB-T:ITIC,,,,,,,,,,,,1.61,,,,64.8,18.7,,,,,,,900\r\n\"Y. Yang, J. Ou, X. Lv, C. Meng, Y. Mai, Sol. Energy 2019, 180, 57.\",9.2,,,,,,,PTB7-Th:PC71BM,,,,,,,,,,,,1.63,,,,74.7,16,,,,,,,770\r\n\"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\",9.3,,,,,,,J51:ITIC,,,,,,,,,,,,1.65,,,,68.7,16.5,,,,,,,820\r\n\"T. Xu, C. Gong, S. Wang, H. Lian, W. Lan, G. Lévêque, B. Grandidier, J. Plain, R. Bachelot, B. Wei, F. Zhu, Sol. RRL 2020, 4, 1900522.\",8.2,,,,,,,PBDB-T:ITIC,,,,,,,,,,,,1.65,,,,68.6,13.4,,,,,,,890\r\n\"C. Xie, X. Jiang, Q. Zhu, D. Wang, C. Xiao, C. Liu, W. Ma, Q. Chen, W. Li, Small Methods 2021, 5, 2100481.\",7.2,,,,,,,JP02,,,,,,,,,,,,1.82,,,,71.3,10.9,,,,,,,925\r\n\"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\",3.7,,,,,,,P3HT:PCBM,,,,,,,,,,,,2.01,,,,59.2,10.4,,,,,,,592\r\n\"K. G. Baiju, B. Murali, R. Subba Rao, K. Jayanarayanan, D. Kumaresan, Chem. Eng. Process. 2020, 149, 107817.\",4.1,,,,,,,,,,,,,,,,,,,1.65,,,,53.9,9.9,,,,N719,,,770\r\n\"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\",4.6,,,,,,,,,,,,,,,,,,,1.74,,,,58,10.5,,,,N719,,,750\r\n\"T. Yamaguchi, N. Tobe, D. Matsumoto, T. Nagai, H. Arakawa, Sol. Energy Mater. Sol. Cells 2010, 94, 812.\",7.6,,,,,,,,,,,,,,,,,,,1.75,,,,69.2,15,,,,N719,,,732\r\n\"F. Huang, D. Chen, Q. Li, R. A. Caruso, Y.-B. Cheng, Appl. Phys. Lett. 2012, 100, 123102.\",7.5,,,,,,,,,,,,,,,,,,,1.78,,,,67.5,15.4,,,,N719,,,725\r\n\"Y. Wang, P. Cheng, C. Feng, H. Zhang, W. Zhao, Sol. Energy 2019, 180, 423.\",6.5,,,,,,,,,,,,,,,,,,,1.79,,,,68,13.2,,,,N719,,,729\r\n\"H. C. Weerasinghe, P. M. Sirimanne, G. P. Simon, Y.-B. Cheng, Prog. Photovoltaic: Res. Appl. 2012, 20, 321.\",6.3,,,,,,,,,,,,,,,,,,,1.8,,,,66,13.1,,,,N719,,,732\r\n\"H. Lee, J. Kim, D. Y. Kim, Y. Seo, Org. Electron. 2018, 52, 103.\",6.3,,,,,,,,,,,,,,,,,,,1.81,,,,67.9,12.3,,,,(JH-1)0.6(SQ2)0.4,,,754\r\n\"H. C. Weerasinghe, P. M. Sirimanne, G. V. Franks, G. P. Simon, Y. B. Cheng, J. Photochem. Photobiol., A 2010, 213, 30.\",5,,,,,,,,,,,,,,,,,,,183,,,,67.8,10,,,,N719,,,735\r\n\"Y. Xiao, J. Wu, G. Yue, J. Lin, M. Huang, Z. Lan, Electrochim. Acta 2011, 56, 8545.\",6,,,,,,,,,,,,,,,,,,,1.88,,,,71,11.2,,,,N719,,,750\r\n\"D. Kishore Kumar, M.-H. Hsu, A. Ivaturi, B. Chen, N. Bennett, H. M. Upadhyaya, Flexible Printed Electron. 2019, 4, 015007.\",4.2,,,,,,,,,,,,,,,,,,,1.9,,,,57.7,10.7,,,,N719,,,680\r\n\"L. Song, Y. Guan, P. Du, Y. Yang, F. Ko, J. Xiong, Sol. Energy Mater. Sol. Cells 2016, 147, 134.\",4.2,,,,,,,,,,,,,,,,,,,1.94,,,,57.2,10.3,,,,N719,,,710\r\n\"H. C. Weerasinghe, G. V. Franks, J. D. Plessis, G. P. Simon, Y.-B. Cheng, J. Mater. Chem. 2010, 20, 9954.\",4.9,,,,,,,,,,,,,,,,,,,1.95,,,,62.3,11.2,,,,N719,,,702\r\n\"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\",6.4,,,,,,,,,,,,,,,,,,,1.99,,,,53.4,18.1,,,,N719,,,660\r\n\"J. H. Kim, S.-J. Yoo, D. Lee, J. W. Choi, S.-C. Han, T. I. Ryu, H. W. Lee, M. Shin, M. Song, Nano Res. 2021, 14, 2728.\",5.4,,,,,,,,,,,,,,,,,,,2.12,,,,76.3,10.4,,,,N719,,,680\r\n\"A. F. Palmstrom, G. E. Eperon, T. Leijtens, R. Prasanna, S. N. Habisreutinger, W. Nemeth, E. A. Gaulding, S. P. Dunfield, M. Reese, S. Nanayakkara, T. Moot, J. Werner, J. Liu, B. To, S. T. Christensen, M. D. McGehee, M. F. A. M. van Hest, J. M. Luther, J. J. Berry, D. T. Moore, Joule 2019, 3, 2193.\",21.3,,,,,,,,,,,,,,FA0.75Cs0.25Sn0.5Pb0.5I3,,,,,,1.73,1.28,,75,15.6,,,,,,FA0.6Cs0.3DMA0.1PbI2.4Br0.6,1820\r\n\"Z. Li, S. Wu, J. Zhang, K. C. Lee, H. Lei, F. Lin, Z. Wang, Z. Zhu, A. K. Y. Jen, Adv. Energy Mater. 2020, 10, 2000361.\",13.6,,,,,,,,,,,,,,PBDB-T:SN6IC-4F,,,,,,1.82,1.4,,68.3,11.1,,,,,,Cs0.1(FA0.6MA0.4)0.9Pb(I0.6Br0.4)3,1800\r\n\"B. M. Kayes, L. Zhang, R. Twist, I. Ding, G. S. Higashi, IEEE J. Photovoltaics 2014, 4, 729.\",30.4,,,,,,,,,,,,,,GaAs,,,,,,1.86,1.41,,84.7,14.3,,,,,,InGaP,2547\r\n\"T. S. Kim, H. J. Kim, D.-M. Geum, J.-H. Han, I. S. Kim, N. Hong, G. H. Ryu, J. Kang, W. J. Choi, K. J. Yu, ACS Appl. Mater. Interfaces 2021, 13, 13248.\",27.4,,,,,,,,,,,,,,GaAs,,,,,,1.92,1.41,,88,13.1,,,,,,InGaP,2400\r\n\"K.-J. Yang, S. Kim, S.-Y. Kim, D.-H. Son, J. Lee, Y.-I. Kim, S.-J. Sung, D.-H. Kim, T. Enkhbat, J. Kim, J. Kim, W. Jo, J.-K. Kang, Adv. Funct. Mater. 2021, n/a, 2102238.\",11.2,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,,1.16,,,,62.8,33.1,,,,,,,539\r\n\"K. Li, F. Li, C. Chen, P. Jiang, S. Lu, S. Wang, Y. Lu, G. Tu, J. Guo, L. Shui, Z. Liu, B. Song, J. Tang, Nano Energy 2021, 86, 106101.\",6.1,,,,,,,,Sb2Se3,,,,,,,,,,,1.32,,,,57.9,25.5,,,,,,,415\r\n\"M. I. Khalil, R. Bernasconi, A. Lucotti, A. Le Donne, R. A. Mereu, S. Binetti, J. L. Hart, M. L. Taheri, L. Nobili, L. Magagnin, J. Appl. Electrochem. 2021, 51, 209.\",0.6,,,,,,,,Cu2ZnSnS4,,,,,,,,,,,1.52,,,,35.5,7.6,,,,,,,204\r\n\"Q. Tang, H. Shen, H. Yao, K. Gao, Y. Jiang, Y. Li, Y. Liu, L. Zhang, Z. Ni, Q. Wei, Renewable Energy 2019, 133, 883.\",17,,,,,,,,,c-Si,,,,,,,,,,1.14,,,,70.8,36.6,,,,,,,656\r\n\"I. Hwang, H.-D. Um, B.-S. Kim, M. Wober, K. Seo, Energy Environ. Sci. 2018, 11, 641.\",18.9,,,,,,,,,c-Si,,,,,,,,,,1.17,,,,63,39.5,,,,,,,608\r\n\"S.-T. Kim, H.-J. Jeong, Y.-C. Kim, V. Bhatt, M. Kumar, J.-H. Yun, J.-H. Jang, Energy Rep. 2021, 7, 2255.\",12,,,,,,,,,CIGS,,,,,,,,,,1.17,,,,58.4,35.8,,,,,,,580\r\n\"A. Chirilă, P. Reinhard, F. Pianezzi, P. Bloesch, A. R. Uhl, C. Fella, L. Kranz, D. Keller, C. Gretener, H. Hagendorfer, D. Jaeger, R. Erni, S. Nishiwaki, S. Buecheler, A. N. Tiwari, Nat. Mater. 2013, 12, 1107.\",20.4,,,,,,,,,CIGS,,,,,,,,,,1.2,,,,78.9,35.1,,,,,,,736\r\n\"R. Kaczynski, J. Lee, J. V. Alsburg, B. Sang, U. Schoop, J. Britt, presented at 2017 IEEE 44th Photovoltaic Spec. Conf. (PVSC), Washington, DC, USA 25–30 June 2017.\",18.7,,,,,,,,,CIGS,,,,,,,,,,1.22,,,,74.4,35,,,,,,,720\r\n\"K. Ruan, K. Ding, Y. Wang, S. Diao, Z. Shao, X. Zhang, J. Jie, J. Mater. Chem. A 2015, 3, 14370.\",8.4,,,,,,,,,c-Si,,,,,,,,,,1.32,,,,63,24.3,,,,,,,550\r\n\"S. Moon, K. Kim, Y. Kim, J. Heo, J. Lee, Sci. Rep. 2016, 6, 30107.\",22.1,,,,,,,,,GaAs,,,,,,,,,,1.42,,,,83.4,27.1,,,,,,,980\r\n\"H. P. Mahabaduge, W. L. Rance, J. M. Burst, M. O. Reese, D. M. Meysing, C. A. Wolden, J. Li, J. D. Beach, T. A. Gessert, W. K. Metzger, S. Garner, T. M. Barnes, Appl. Phys. Lett. 2015, 106, 133501.\",16.4,,,,,,,,,CdTe,,,,,,,,,,1.46,,,,77.4,25.5,,,,,,,831\r\n\"L. Kranz, C. Gretener, J. Perrenoud, R. Schmitt, F. Pianezzi, F. La Mattina, P. Blösch, E. Cheah, A. Chirilă, C. M. Fella, H. Hagendorfer, T. Jäger, S. Nishiwaki, A. R. Uhl, S. Buecheler, A. N. Tiwari, Nat. Commun. 2013, 4, 2306.\",11.5,,,,,,,,,CdTe,,,,,,,,,,1.49,,,,63.9,22,,,,,,,821\r\n\"T. Söderström, F.-J. Haug, V. Terrazzoni-Daudrix, C. Ballif, J. Appl. Phys. 2008, 103, 114509.\",8.8,,,,,,,,,a-Si:H,,,,,,,,,,1.79,,,,70,14.3,,,,,,,888\r\n\"C. Zhang, Y. Song, M. Wang, M. Yin, X. Zhu, L. Tian, H. Wang, X. Chen, Z. Fan, L. Lu, D. Li, Adv. Funct. Mater. 2017, 27, 1604720.\",8.2,,,,,,,,,a-Si:H,,,,,,,,,,1.88,,,,64,15.6,,,,,,,820\r\n\"S.-H. Lim, H.-J. Seok, M.-J. Kwak, D.-H. Choi, S.-K. Kim, D.-H. Kim, H.-K. Kim, Nano Energy 2021, 82, 105703.\",15.7,,,,,3,Cs0.175FA0.75MA0.075Pb (I0.875Br0.125)3,,,,,,,,,,,,,1.64,,,,77.2,19,,,,,,,1070\r\n\"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\",12.2,,,,,3,MAPbI3,,,,,,,,,,,,,1.53,,,,68.5,17.5,,,,,,,1017\r\n\"Z. Ying, X. Yang, J. Zheng, Y. Zhu, J. Xiu, W. Chen, C. Shou, J. Sheng, Y. Zeng, B. Yan, H. Pan, J. Ye, Z. He, J. Mater. Chem. A 2021, 9, 12009.\",18.2,,,,,4,CsFAMAPb(IBr)3,,,,,,,,,,,,,1.63,,,,80,21.1,,,,,,,1076\r\n\"B. Chen, Y. Bai, Z. Yu, T. Li, X. Zheng, Q. Dong, L. Shen, M. Boccard, A. Gruverman, Z. Holman, J. Huang, Adv. Energy Mater. 2016, 6, 1601128.\",16.5,,,,,5,MAPbI3,,,,,,,,,,,,,1.6,,,,74.2,20.6,,,,,,,1080\r\n\"P. You, Z. Liu, Q. Tai, S. Liu, F. Yan, Adv. Mater. 2015, 27, 3632.\",12,,,,,5,MAPbI3−xClx,,,,,,,,,,,,,1.61,,,,65.3,19.2,,,,,,,960\r\n\"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\",11.2,,,,,5,MAPbI3,,,,,,,,,,,,,1.65,,,,64.9,18.4,,,,,,,940\r\n\"J. H. Heo, H. J. Han, M. Lee, M. Song, D. H. Kim, S. H. Im, Energy Environ. Sci. 2015, 8, 2922.\",15.8,,,,,6,MAPbI3,,,,,,,,,,,,,1.6,,,,74.4,19.3,,,,,,,1100\r\n\"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\",13.6,,,,,7,MAPbI3,,,,,,,,,,,,,1.55,,,,67.5,20.4,,,,,,,988\r\n\"D. Yang, X. Zhang, Y. Hou, K. Wang, T. Ye, J. Yoon, C. Wu, M. Sanghadasa, S. Liu, S. Priya, Nano Energy 2021, 84, 105934.\",19.8,,,,,8,Cs0.05FA0.95PbI3,,,,,,,,,,,,,1.52,,,,79.5,21.9,,,,,,,1137\r\n\"S.-H. Lim, H.-J. Seok, M.-J. Kwak, D.-H. Choi, S.-K. Kim, D.-H. Kim, H.-K. Kim, Nano Energy 2021, 82, 105703.\",17.4,,,,,9,Cs0.175FA0.825Pb(I0.875Br0.125)3,,,,,,,,,,,,,1.64,,,,75.1,21.5,,,,,,,1083\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",17.5,,,,,10,MAPbI3,,,,,,,,,,,,,1.59,,,,73.1,22.4,,,,,,,1070\r\n\"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\",16.1,,,,,10,Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.65,,,,74.5,20.4,,,,,,,1060\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",13.2,,,,,12,MAPbI3,,,,,,,,,,,,,1.6,,,,67.8,19.5,,,,,,,1000\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",14.9,,,,,13,MAPbI2.5Br0.5,,,,,,,,,,,,,1.67,,,,68.4,19.8,,,,,,,1100\r\n\"S.-H. Lim, H.-J. Seok, M.-J. Kwak, D.-H. Choi, S.-K. Kim, D.-H. Kim, H.-K. Kim, Nano Energy 2021, 82, 105703.\",13.6,,,,,14,Cs0.175FA0.825Pb(I0.875Br0.125)3,,,,,,,,,,,,,1.64,,,,78.6,16.5,,,,,,,1048\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",13,,,,,14,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,69.9,19.1,,,,,,,970\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",11.9,,,,,15,MAPbI3,,,,,,,,,,,,,1.61,,,,66.3,17.8,,,,,,,1000\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",13.7,,,,,16,MAPbI2Br,,,,,,,,,,,,,1.76,,,,73.4,16.7,,,,,,,1120\r\n\"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\",12.8,,,,,17,Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.65,,,,74.1,16.6,,,,,,,1040\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",12.2,,,,,18,MAPbI2Br,,,,,,,,,,,,,1.77,,,,72.7,15.1,,,,,,,1110\r\n\"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\",9.1,,,,,18,MAPbI3,,,,,,,,,,,,,1.53,,,,61.5,14.6,,,,,,,1017\r\n\"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\",8.8,,,,,19,MAPbI3,,,,,,,,,,,,,1.55,,,,68.3,13.7,,,,,,,941\r\n\"Y.-W. Zhang, P.-P. Cheng, W.-Y. Tan, Y. Min, Appl. Surf. Sci. 2021, 537, 147908.\",11.7,,,,,20,MAPbI3+ BiPy − I,,,,,,,,,,,,,1.63,,,,74.6,14.5,,,,,,,1080\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",14.7,,,,,20,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.63,,,,75.2,17.6,,,,,,,1108\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",14.2,,,,,21,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.63,,,,73.2,17.4,,,,,,,1117\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",13.2,,,,,22,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.61,,,,71.7,17.2,,,,,,,1073\r\n\"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\",12.3,,,,,23,KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.61,,,,66.6,17.1,,,,,,,1082\r\n\"S. Xiao, H. Chen, F. Jiang, Y. Bai, Z. Zhu, T. Zhang, X. Zheng, G. Qian, C. Hu, Y. Zhou, Y. Qu, S. Yang, Adv. Mater. Interfaces 2016, 3, 1600484.\",11.3,,,,,23,MAPbI3,,,,,,,,,,,,,1.62,,,,72.3,15.1,,,,,,,1040\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",10.8,,,,,23,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,64.4,17.3,,,,,,,970\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",9.4,,,,,24,MAPbI1.5Br1.5,,,,,,,,,,,,,1.87,,,,61.6,13.6,,,,,,,1120\r\n\"C.-Y. Chang, K.-T. Lee, W.-K. Huang, H.-Y. Siao, Y.-C. Chang, Chem. Mater. 2015, 27, 5122.\",10.8,,,,,25,MAPbI3,,,,,,,,,,,,,1.55,,,,69.7,16.3,,,,,,,950\r\n\"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\",10.2,,,,,26,MAPbI3,,,,,,,,,,,,,1.63,,,,78.1,12.2,,,,,,,1070\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",12.1,,,,,27,MAPbI3,,,,,,,,,,,,,1.6,,,,66.2,18.3,,,,,,,1000\r\n\"F. Guo, H. Azimi, Y. Hou, T. Przybilla, M. Hu, C. Bronnbauer, S. Langner, E. Spiecker, K. Forberich, C. J. Brabec, Nanoscale 2015, 7, 1642.\",8.5,,,,,28,MAPbI3−xClx,,,,,,,,,,,,,1.6,,,,66.8,13.1,,,,,,,964\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",8.1,,,,,28,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,70.2,11.2,,,,,,,1030\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",12.8,,,,,30,MAPbI3−xClx,,,,,,,,,,,,,1.62,,,,74.9,16.5,,,,,,,1030\r\n\"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\",7.4,,,,,30,Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3,,,,,,,,,,,,,1.65,,,,62.2,11.8,,,,,,,1010\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",11.9,,,,,31,MAPbI2.5Br0.5,,,,,,,,,,,,,1.69,,,,69.4,16.3,,,,,,,1050\r\n\"C. Roldán-Carmona, O. Malinkiewicz, R. Betancur, G. Longo, C. Momblona, F. Jaramillo, L. Camacho, H. J. Bolink, Energy Environ. Sci. 2014, 7, 2968.\",7.3,,,,,33,MAPbI3,,,,,,,,,,,,,1.55,,,,52.5,13.4,,,,,,,1037\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",11.7,,,,,34,MAPbI3−xClx,,,,,,,,,,,,,1.62,,,,74.6,15.9,,,,,,,990\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",10.3,,,,,36,MAPbI2Br,,,,,,,,,,,,,1.79,,,,65.5,14.6,,,,,,,1080\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",10.8,,,,,37,MAPbI3−xClx,,,,,,,,,,,,,1.62,,,,73.1,14.7,,,,,,,1010\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",7.8,,,,,37,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,69.6,11.6,,,,,,,970\r\n\"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\",10.7,,,,,38,MAPbI3,,,,,,,,,,,,,1.63,,,,77.6,13,,,,,,,1060\r\n\"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\",8.8,,,,,41,MAPbI1.5Br1.5,,,,,,,,,,,,,1.9,,,,62.2,12.8,,,,,,,1110\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",10.3,,,,,42,MAPbI3−xClx,,,,,,,,,,,,,1.63,,,,75.6,13.6,,,,,,,1000\r\n\"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\",8.5,,,,,45,MAPbI3−xClx,,,,,,,,,,,,,1.64,,,,73.5,12.6,,,,,,,960\r\n\"C. O. Ramírez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heumüller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\",3.6,,,,,46,MAPbI3−xClx,,,,,,,,,,,,,1.57,,,,64.4,5.4,,,,,,,1030\r\n\"S. Bag, M. F. Durstock, Nano Energy 2016, 30, 542.\",4.5,,,,,47,MAPbI3,,,,,,,,,,,,,1.63,,,,63,8.2,,,,,,,880\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.1,,,,,66,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,52.9,2.1,,,,,,,1000\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",7.8,,,,,68,FAPbBr2.43Cl0.57,,,,,,,,,,,,,2.35,,,,72,6.7,,,,,,,1550\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.5,,,,,72,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,74.3,2.1,,,,,,,960\r\n\"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\",0.2,,,,,72,MAPbCl3,,,,,,,,,,,,,3.03,,,,35.4,0.6,,,,,,,1110\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.6,,,,,73,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,73.1,2.2,,,,,,,970\r\n\"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\",0.5,,,,,73,MAPbCl2.4Br0.6,,,,,,,,,,,,,2.84,,,,44.9,0.9,,,,,,,1260\r\n\"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\",1.5,,,,,74,Cs2AgBiBr6,,,,,,,,,,,,,2.62,,,,71.1,2.2,,,,,,,970\r\n\"Y.-M. Sung, M.-Z. Li, D. Luo, Y.-D. Li, S. Biring, Y.-C. Huang, C.-K. Wang, S.-W. Liu, K.-T. Wong, Nano Energy 2021, 80, 105565.\",13.3,,,,,1,,,,,,PM6:Y6,,,,,,,,1.4,,,,66.5,24.6,,,,,,,810\r\n\"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\",7.6,,,,,2,,,,,,PBDTTT-C-T:PC71BM,,,,,,,,1.66,,,,63.3,15.6,,,,,,,770\r\n\"Y.-M. Sung, M.-Z. Li, D. Luo, Y.-D. Li, S. Biring, Y.-C. Huang, C.-K. Wang, S.-W. Liu, K.-T. Wong, Nano Energy 2021, 80, 105565.\",12.6,,,,,3,,,,,,PM6:Y6,,,,,,,,1.4,,,,64.5,24.5,,,,,,,800\r\n\"C.-K. Wang, B.-H. Jiang, J.-H. Lu, M.-T. Cheng, R.-J. Jeng, Y.-W. Lu, C.-P. Chen, K.-T. Wong, ChemSusChem 2020, 13, 903.\",12,,,,,6,,,,,,PM7/PTTtID-Cl/IT-4F,,,,,,,,1.47,,,,70.4,19.6,,,,,,,870\r\n\"Y.-M. Sung, M.-Z. Li, D. Luo, Y.-D. Li, S. Biring, Y.-C. Huang, C.-K. Wang, S.-W. Liu, K.-T. Wong, Nano Energy 2021, 80, 105565.\",7.3,,,,,8,,,,,,DTDCPB:C70,,,,,,,,1.73,,,,69.6,12.1,,,,,,,860\r\n\"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\",14.2,,,,,9,,,,,,PM6:Y6,,,,,,,,1.42,,,,72.3,23,,,,,,,854\r\n\"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\",7.1,,,,,11,,,,,,PBDTTT-C-T:PC71BM,,,,,,,,1.66,,,,64.4,14.5,,,,,,,760\r\n\"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\",13.3,,,,,13,,,,,,PM6:Y6,,,,,,,,1.42,,,,71.9,21.7,,,,,,,853\r\n\"X. Li, R. Xia, K. Yan, J. Ren, H.-L. Yip, C.-Z. Li, H. Chen, ACS Energy Lett. 2020, 5, 3115.\",13.6,,,,,14,,,,,,PM6:Y6,,,,,,,,1.4,,,,75.8,21.1,,,,,,,850\r\n\"W. Song, Y. Liu, B. Fanady, Y. Han, L. Xie, Z. Chen, K. Yu, X. Peng, X. Zhang, Z. Ge, Nano Energy 2021, 86, 106044.\",12,,,,,14,,,,,,PM6:Y6:C6,,,,,,,,1.41,,,,72.8,19.6,,,,,,,844\r\n\"T. Xiao, J. Wang, S. Yang, Y. Zhu, D. Li, Z. Wang, S. Feng, L. Bu, X. Zhan, G. Lu, J. Mater. Chem. A 2020, 8, 401.\",8.9,,,,,15,,,,,,PTB7-Th:FNIC1,,,,,,,,1.52,,,,63,18.3,,,,,,,772\r\n\"S. Wageh, M. Raïssi, T. Berthelot, A. A. Al-Ghamdi, A. M. Abusorrah, W. Boukhili, O. A. Al-Hartomy, Adv. Eng. Mater. 2021, 23, 2001305.\",2.9,,,,,16,,,,,,P3HT-PCBM,,,,,,,,1.95,,,,55.4,9.7,,,,,,,540\r\n\"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\",12.6,,,,,17,,,,,,PBDB-T-2F:Y6,,,,,,,,1.39,,,,73.2,21.2,,,,,,,810\r\n\"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\",11.7,,,,,18,,,,,,PBDB-T-2F:Y6,,,,,,,,1.39,,,,69.6,20.7,,,,,,,810\r\n\"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\",12.4,,,,,19,,,,,,PM6:Y6,,,,,,,,1.42,,,,71.4,20.4,,,,,,,852\r\n\"Y. Bai, C. Zhao, R. Shi, J. Wang, F. Wang, T. Hayat, A. Alsaedi, Z. a. Tan, Mater. Chem. Front. 2020, 4, 2072.\",12.3,,,,,20,,,,,,PM6:Y6,,,,,,,,1.42,,,,73,20.6,,,,,,,817\r\n\"L. Chang, L. Duan, M. Sheng, J. Yuan, H. Yi, Y. Zou, A. Uddin, Nanomaterials 2020, 10, 1759.\",13.8,,,,,21,,,,,,PM6:N3,,,,,,,,1.41,,,,66.5,25.3,,,,,,,820\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\",11,,,,,25,,,,,,PCE-10:A078,,,,,,,,1.34,,,,70,20.9,,,,,,,750\r\n\"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\",10.2,,,,,25,,,,,,PTB7-Th:FOIC,,,,,,,,1.4,,,,68.3,20.3,,,,,,,736\r\n\"Y. Bai, C. Zhao, X. Chen, S. Zhang, S. Zhang, T. Hayat, A. Alsaedi, Z. a. Tan, J. Hou, Y. Li, J. Mater. Chem. A 2019, 7, 15887.\",12.9,,,,,26,,,,,,PBDB-T-2F:Y6,,,,,,,,1.4,,,,72.4,21.6,,,,,,,825\r\n\"L. Chang, L. Duan, M. Sheng, J. Yuan, H. Yi, Y. Zou, A. Uddin, Nanomaterials 2020, 10, 1759.\",8.9,,,,,28,,,,,,PM6:N3,,,,,,,,1.41,,,,65.1,16.8,,,,,,,810\r\n\"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\",5.6,,,,,28,,,,,,PBDTTT-C-T:PC71BM,,,,,,,,1.66,,,,61.9,11.9,,,,,,,760\r\n\"L. Chang, L. Duan, M. Sheng, J. Yuan, H. Yi, Y. Zou, A. Uddin, Nanomaterials 2020, 10, 1759.\",7.8,,,,,29,,,,,,PM6:N3,,,,,,,,1.41,,,,64.7,15.2,,,,,,,800\r\n\"R. Xia, C. J. Brabec, H.-L. Yip, Y. Cao, Joule 2019, 3, 2241.\",10.8,,,,,30,,,,,,PTB7-Th:IEICO-4F,,,,,,,,1.35,,,,68.7,21.9,,,,,,,718\r\n\"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\",9.1,,,,,34,,,,,,PTB7-Th:FOIC,,,,,,,,1.4,,,,67.1,18.5,,,,,,,733\r\n\"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\",8.8,,,,,36,,,,,,PCE-10:BT-CIC:TT-FIC,,,,,,,,1.37,,,,71.9,18,,,,,,,680\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",6.9,,,,,36,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,66.5,11.6,,,,,,,890\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",6.1,,,,,37,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,66.8,10.2,,,,,,,890\r\n\"S. Song, H. W. Cho, J. Jeong, Y. J. Yoon, S. Y. Park, S. Song, B. H. Woo, Y. C. Jun, B. Walker, J. Y. Kim, Sol. RRL 2020, 4, 2000201.\",5.7,,,,,38,,,,,,PTB7-Th:IEICO-4F,,,,,,,,1.33,,,,66.2,12.4,,,,,,,700\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",4.9,,,,,39,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,67.9,8.3,,,,,,,880\r\n\"D. Corzo, E. Bihar, E. B. Alexandre, D. Rosas-Villalva, D. Baran, Adv. Funct. Mater. 2021, 31, 2005763.\",9.6,,,,,42,,,,,,PTB7-Th:IEICO-4F,,,,,,,,1.35,,,,53.2,26.1,,,,,,,690\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\",8.1,,,,,43,,,,,,PCE-10:A078,,,,,,,,1.34,,,,68.1,16.3,,,,,,,730\r\n\"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\",8,,,,,44,,,,,,PCE-10:BT-CIC:TT-FIC,,,,,,,,1.37,,,,72.6,16.2,,,,,,,680\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\",10.8,,,,,46,,,,,,PCE-10:A078,,,,,,,,1.34,,,,70.6,20.4,,,,,,,750\r\n\"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\",7.1,,,,,47,,,,,,PCE-10:A078,,,,,,,,1.34,,,,68,14.3,,,,,,,730\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",2.4,,,,,47,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,68.2,4.1,,,,,,,860\r\n\"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\",7.2,,,,,49,,,,,,PCE-10:BT-CIC:TT-FIC,,,,,,,,1.37,,,,72.6,14.8,,,,,,,670\r\n\"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\",8.3,,,,,50,,,,,,PTB7-Th:FOIC:PC71BM,,,,,,,,1.38,,,,66.8,16.7,,,,,,,746\r\n\"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\",7.4,,,,,51,,,,,,PTB7-Th:FOIC:PC71BM,,,,,,,,1.39,,,,66.7,14.7,,,,,,,749\r\n\"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\",1.8,,,,,53,,,,,,PSEHTT:ICBA,,,,,,,,1.86,,,,54.8,3.8,,,,,,,890\r\n\"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\",5.7,,,,,53,,,,,,DPP2T:IEICO-4F,,,,,,,,1.32,,,,69.5,10.6,,,,,,,750\r\n\"N. Chaturvedi, N. Gasparini, D. Corzo, J. Bertrandie, N. Wehbe, J. Troughton, D. Baran, Adv. Funct. Mater. 2021, 31, 2009996.\",9.1,,,,,60,,,,,,PTB7-Th:IEICO-4F,,,,,,,,1.32,,,,59.1,22.6,,,,,,,680\r\n\"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\",3.9,,,,,60,,,,,,DPP2T:IEICO-4F,,,,,,,,1.33,,,,70.2,7.3,,,,,,,749\r\n\"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\",5.9,,,,,62,,,,,,PTB7-Th:6TIC-4F,,,,,,,,1.33,,,,66,12.9,,,,,,,690\r\n\"C. Yang, M. Moemeni, M. Bates, W. Sheng, B. Borhan, R. R. Lunt, Adv. Opt. Mater. 2020, 8, 1901536.\",1.2,,,,,73,,,,,,COi8DFIC,,,,,,,,1.5,,,,81,1.5,,,,,,,990\r\n\"Y. Zhao, R. R. Lunt, Adv. Energy Mater. 2013, 3, 1143.\",0.4,,,,,84,,,,,,PBMMA:PEMA:(TBA)2Mo6Cl14,,,,,,,,2.81,,,,65,1.3,,,,,,,520\r\n\"Y. Zhao, G. A. Meek, B. G. Levine, R. R. Lunt, Adv. Opt. Mater. 2014, 2, 606.\",0.4,,,,,86,,,,,,Cy7,,,,,,,,1.52,,,,66,1.2,,,,,,,500\r\n\"C. López-López, S. Colodrero, H. Míguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\",5.2,,,,,1,,,,,,,,,,,,,,2,,,,53.7,12.4,,,,N719,,,780\r\n\"C. López-López, S. Colodrero, H. Míguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\",4.5,,,,,9,,,,,,,,,,,,,,2,,,,56,10.3,,,,N719,,,780\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",4.3,,,,,9,,,,,,,,,,,,,,1.82,,,,60,9.9,,,,N719+SDA,,,720\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",5.2,,,,,10,,,,,,,,,,,,,,2.01,,,,57,11.9,,,,N719,,,770\r\n\"C. López-López, S. Colodrero, H. Míguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\",4.9,,,,,10,,,,,,,,,,,,,,2,,,,56.1,11.4,,,,N719,,,765\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",10.1,,,,,13,,,,,,,,,,,,,,1.68,,,,80.2,14.9,,,,SGT-021,,,851\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",9.9,,,,,14,,,,,,,,,,,,,,1.68,,,,78.5,14.9,,,,SGT-021,,,850\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",9.6,,,,,15,,,,,,,,,,,,,,1.68,,,,77.2,14.7,,,,SGT-021,,,850\r\n\"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\",9.8,,,,,17,,,,,,,,,,,,,,1.68,,,,75.5,15.1,,,,SGT-021,,,855\r\n\"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\",8.6,,,,,18,,,,,,,,,,,,,,2,,,,68.4,16.7,,,,N719 (EtOH),,,750\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",4.2,,,,,23,,,,,,,,,,,,,,1.82,,,,64,9.9,,,,N719+SDA,,,650\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",3.6,,,,,23,,,,,,,,,,,,,,2.01,,,,68,8.2,,,,N719,,,650\r\n\"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\",7.8,,,,,24,,,,,,,,,,,,,,2,,,,56.3,17.4,,,,N719 (EtOH),,,794\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",2.6,,,,,25,,,,,,,,,,,,,,1.82,,,,71,5.6,,,,N719+SDA,,,650\r\n\"Q. Huaulmé, V. M. Mwalukuku, D. Joly, J. Liotier, Y. Kervella, P. Maldivi, S. Narbey, F. Oswald, A. J. Riquelme, J. A. Anta, R. Demadrille, Nat. Energy 2020, 5, 468.\",3.7,,,,,27,,,,,,,,,,,,,,1.77,,,,65.8,10.7,,,,NPI,,,521\r\n\"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\",1.5,,,,,30,,,,,,,,,,,,,,2.19,,,,70,3.3,,,,N719,,,640\r\n\"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\",6.4,,,,,31,,,,,,,,,,,,,,2.23,,,,67.9,13.5,,,,TPA-1 (EtOH),,,698\r\n\"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\",6.1,,,,,33,,,,,,,,,,,,,,2.3,,,,68.3,12.5,,,,TPA-2 (EtOH),,,711\r\n\"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\",6.1,,,,,36,,,,,,,,,,,,,,2.23,,,,54.7,14.5,,,,TPA-1 (EtOH),,,766\r\n\"D. A. Chalkias, C. Charalampopoulos, S. Aivali, A. K. Andreopoulou, A. Karavioti, E. Stathatos, Energies 2021, 14, 1159.\",3.5,,,,,37,,,,,,,,,,,,,,2.46,,,,67.5,8,,,,Cz-2,,,648\r\n\"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\",5.7,,,,,38,,,,,,,,,,,,,,2.31,,,,54.2,13.6,,,,TPA-2 (EtOH),,,769\r\n\"K. Kim, S. K. Nam, J. H. Moon, ACS Appl. Energy Mater. 2020, 3, 5277.\",7.8,,,,,43,,,,,,,,,,,,,,1.95,,,,70.8,15.3,,,,PdTPBP/BPEA,,,720\r\n\"W. Naim, V. Novelli, I. Nikolinakos, N. Barbero, I. Dzeba, F. Grifoni, Y. Ren, T. Alnasser, A. Velardo, R. Borrelli, S. Haacke, S. M. Zakeeruddin, M. Graetzel, C. Barolo, F. Sauvage, JACS Au 2021, 1, 409.\",3.1,,,,,69,,,,,,,,,,,,,,1.39,,,,65.6,11.2,,,,VG20-C16,,,422\r\n\"W. Naim, V. Novelli, I. Nikolinakos, N. Barbero, I. Dzeba, F. Grifoni, Y. Ren, T. Alnasser, A. Velardo, R. Borrelli, S. Haacke, S. M. Zakeeruddin, M. Graetzel, C. Barolo, F. Sauvage, JACS Au 2021, 1, 409.\",2.3,,,,,76,,,,,,,,,,,,,,1.41,,,,65.9,8.6,,,,VG20-C16,,,406\r\n\"S. W. Leow, W. Li, J. M. R. Tan, S. Venkataraj, V. Tunuguntla, M. Zhang, S. Magdassi, L. H. Wong, Sol. RRL 2021, n/a, 2100131.\",3,,,,,1,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.46,,,,42.8,14.6,,,,,,,475\r\n\"S.-J. Lee, S.-J. Sung, K.-J. Yang, J.-K. Kang, J. Y. Kim, Y. S. Do, D.-H. Kim, ACS Appl. Energy Mater. 2020, 3, 12644.\",3.4,,,,,8,,,,Sb2S3,,,,,,,,,,1.83,,,,42,12.1,,,,,,,679\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",10,,,,,2,,,,CIGS,,,,,,,,,,1.23,,,,66.9,23.3,,,,,,,640\r\n\"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\",9.8,,,,,5,,,,CIGS,,,,,,,,,,1.26,,,,67.6,22.9,,,,,,,630\r\n\"J. Kim, J. W. Lim, G. Kim, M. Shin, ACS Appl. Mater. Interfaces 2021, 13, 4968.\",6.6,,,,,7,,,,a-Si:H,,,,,,,,,,1.92,,,,63.7,11.8,,,,,,,881\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",9.8,,,,,9,,,,CIGS,,,,,,,,,,1.3,,,,74.1,20.9,,,,,,,630\r\n\"K. Kim, W. N. Shafarman, Nano Energy 2016, 30, 488.\",6.5,,,,,9,,,,CIGS,,,,,,,,,,1.28,,,,46.5,22.9,,,,,,,597\r\n\"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\",8.4,,,,,11,,,,CIGS,,,,,,,,,,1.34,,,,66.3,20.4,,,,,,,620\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.5,,,,,16,,,,a-Si:H,,,,,,,,,,1.83,,,,65.3,14.2,,,,,,,810\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.7,,,,,17,,,,a-Si:H,,,,,,,,,,1.83,,,,67.3,14.1,,,,,,,810\r\n\"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\",5.9,,,,,18,,,,a-SiGe:H,,,,,,,,,,2.05,,,,58.3,14.1,,,,,,,720\r\n\"M. Saifullah, S. Ahn, J. Gwak, S. Ahn, K. Kim, J. Cho, J. H. Park, Y. J. Eo, A. Cho, J.-S. Yoo, J. H. Yun, J. Mater. Chem. A 2016, 4, 10542.\",5.9,,,,,18,,,,CIGS,,,,,,,,,,1.5,,,,57.4,14.6,,,,,,,710\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.3,,,,,19,,,,a-Si:H,,,,,,,,,,1.87,,,,67.6,13.1,,,,,,,820\r\n\"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\",6.9,,,,,19,,,,CIGS,,,,,,,,,,1.3,,,,64.7,16.6,,,,,,,640\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",6.5,,,,,19,,,,CIGS,,,,,,,,,,1.34,,,,63.5,17.5,,,,,,,580\r\n\"S. H. Moon, S. J. Park, Y. J. Hwang, D.-K. Lee, Y. Cho, D.-W. Kim, B. K. Min, Sci. Rep. 2014, 4, 4408.\",1.7,,,,,20,,,,CIGS,,,,,,,,,,1.64,,,,40.8,8.9,,,,,,,495\r\n\"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\",5.5,,,,,22,,,,a-Si:H,,,,,,,,,,2.05,,,,58.6,12.3,,,,,,,760\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",6,,,,,23,,,,a-Si:H,,,,,,,,,,1.92,,,,68.2,10.6,,,,,,,830\r\n\"J. Wook Lim, M. Shin, D. J. Lee, S. Hyun Lee, S. Jin Yun, Sol. Energy Mater. Sol. Cells 2014, 128, 301.\",6.9,,,,,24,,,,a-Si:H,,,,,,,,,,1.68,,,,70.3,10.7,,,,,,,920\r\n\"A. Mutalikdesai, S. K. Ramasesha, Thin Solid Films 2017, 632, 73.\",0.4,,,,,37,,,,CdTe,,,,,,,,,,1.54,,,,27.2,14.7,,,,,,,101\r\n\"S. Kim, J. Yi, J. Kim, Sol. RRL 2021, n/a, 2100162.\",1.1,,,,,41,,,,a-Si:H,,,,,,,,,,2.17,,,,47.3,3.9,,,,,,,596\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",10,,,,,2,,,,CIGS,,,,,,,,,,1.23,,,,66.9,23.3,,,,,,,640\r\n\"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\",9.8,,,,,5,,,,CIGS,,,,,,,,,,1.26,,,,67.6,22.9,,,,,,,630\r\n\"J. Kim, J. W. Lim, G. Kim, M. Shin, ACS Appl. Mater. Interfaces 2021, 13, 4968.\",6.6,,,,,7,,,,a-Si:H,,,,,,,,,,1.92,,,,63.7,11.8,,,,,,,881\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",9.8,,,,,9,,,,CIGS,,,,,,,,,,1.3,,,,74.1,20.9,,,,,,,630\r\n\"K. Kim, W. N. Shafarman, Nano Energy 2016, 30, 488.\",6.5,,,,,9,,,,CIGS,,,,,,,,,,1.28,,,,46.5,22.9,,,,,,,597\r\n\"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\",8.4,,,,,11,,,,CIGS,,,,,,,,,,1.34,,,,66.3,20.4,,,,,,,620\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.5,,,,,16,,,,a-Si:H,,,,,,,,,,1.83,,,,65.3,14.2,,,,,,,810\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.7,,,,,17,,,,a-Si:H,,,,,,,,,,1.83,,,,67.3,14.1,,,,,,,810\r\n\"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\",5.9,,,,,18,,,,a-SiGe:H,,,,,,,,,,2.05,,,,58.3,14.1,,,,,,,720\r\n\"M. Saifullah, S. Ahn, J. Gwak, S. Ahn, K. Kim, J. Cho, J. H. Park, Y. J. Eo, A. Cho, J.-S. Yoo, J. H. Yun, J. Mater. Chem. A 2016, 4, 10542.\",5.9,,,,,18,,,,CIGS,,,,,,,,,,1.5,,,,57.4,14.6,,,,,,,710\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",7.3,,,,,19,,,,a-Si:H,,,,,,,,,,1.87,,,,67.6,13.1,,,,,,,820\r\n\"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\",6.9,,,,,19,,,,CIGS,,,,,,,,,,1.3,,,,64.7,16.6,,,,,,,640\r\n\"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\",6.5,,,,,19,,,,CIGS,,,,,,,,,,1.34,,,,63.5,17.5,,,,,,,580\r\n\"S. H. Moon, S. J. Park, Y. J. Hwang, D.-K. Lee, Y. Cho, D.-W. Kim, B. K. Min, Sci. Rep. 2014, 4, 4408.\",1.7,,,,,20,,,,CIGS,,,,,,,,,,1.64,,,,40.8,8.9,,,,,,,495\r\n\"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\",5.5,,,,,22,,,,a-Si:H,,,,,,,,,,2.05,,,,58.6,12.3,,,,,,,760\r\n\"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\",6,,,,,23,,,,a-Si:H,,,,,,,,,,1.92,,,,68.2,10.6,,,,,,,830\r\n\"J. Wook Lim, M. Shin, D. J. Lee, S. Hyun Lee, S. Jin Yun, Sol. Energy Mater. Sol. Cells 2014, 128, 301.\",6.9,,,,,24,,,,a-Si:H,,,,,,,,,,1.68,,,,70.3,10.7,,,,,,,920\r\n\"A. Mutalikdesai, S. K. Ramasesha, Thin Solid Films 2017, 632, 73.\",0.4,,,,,37,,,,CdTe,,,,,,,,,,1.54,,,,27.2,14.7,,,,,,,101\r\n\"S. Kim, J. Yi, J. Kim, Sol. RRL 2021, n/a, 2100162.\",1.1,,,,,41,,,,a-Si:H,,,,,,,,,,2.17,,,,47.3,3.9,,,,,,,596\r\n\"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\",,7.8,7.2,6.8,,,,,,,,PBDB-T:ITIC-2F,,,,\"OC, w-LED, N2, 40 °C, UV-f\",,1.5,7,1.56,,,,,,,,,,,,\r\n\"C. Xie, T. Heumüller, W. Gruber, X. Tang, A. Classen, I. Schuldes, M. Bidwell, A. Späth, R. H. Fink, T. Unruh, I. McCulloch, N. Li, C. J. Brabec, Nat. Commun. 2018, 9, 5335.\",,5,5,4.7,,,,,,,,P3HT:o-IDTBR,,,,\"OC, AM1.5G, N2, UV-f\",,1,4.8,1.57,,,,,,,,,,,,\r\n\"['A. Aubele, Y. He, T. Kraus, N. Li, E. Mena-Osteritz, P. Weitz, T. Heumüller, K. Zhang, C. J. Brabec, P. Bäuerle, Adv. Mater. 2021, n/a, 2103573.', 'Additional Supporting Information: Molecular Oligothiophene–Fullerene Dyad Reaching Over 5% Efficiency in Single-Material Organic Solar Cells, https://emerging-pv.org/wp-content/uploads/2021/09/ASI_stability-OPV_10.1002adma.202103573.pdf (accessed: September 2021).']\",,5.1,4.9,4.9,,,,,,,,Dyad 4,,,,\"OC, w-LED, N2, 30 °C\",,1.1,4.9,1.61,,,,,,,,,,,,\r\n\"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\",,8,7.4,7,,,,,,,,PBDB-T:ITIC-Th,,,,\"OC, w-LED, N2, 40 °C, UV-f\",,1.5,7.3,1.66,,,,,,,,,,,,\r\n\"A. Classen, T. Heumueller, I. Wabra, J. Gerner, Y. He, L. Einsiedler, N. Li, G. J. Matt, A. Osvet, X. Du, A. Hirsch, C. J. Brabec, Adv. Energy Mater. 2019, 9, 1902124.\",,8.7,8.1, ,,,,,,,,PBDB-T:IDTBR,,,,\"OC, AM1.5G, N2, 35–40 °C\",,1.6, ,1.7,,,,,,,,,,,,\r\n\"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\",,5.9,5.6,5.4,,,,,,,,PBDB-T:PCBM,,,,\"OC, w-LED, N2, 40 °C, UV-f\",,1.1,5.6,1.84,,,,,,,,,,,,\r\n\"M. Raïssi, S. Leroy-Lhez, B. Ratier, Org. Electron. 2016, 37, 183.\",,3.7,3.7,3.7,,,,,,,,P3HT-PCBM,,,,\"OC, AM1.5G, air\",,0.7,3.7,1.94,,,,,,,,,,,,\r\n\"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\",,9,9,8.2,,,,,,,,,,,,\"OC, AM1.5G, 65 °C\",,1.8,8.7,1.59,,,,,,,,,TF-tBu_C3F7,,,\r\n\"S. G. Hashmi, M. Özkan, J. Halme, S. M. Zakeeruddin, J. Paltakari, M. Grätzel, P. D. Lund, Energy Environ. Sci. 2016, 9, 2453.\",,6.5,6.7,6.3,,,,,,,,,,,,\"OC, AM1.5G, 35 °C, UV-f\",,1.4,6.6,1.75,,,,,,,,,N719,,,\r\n\"R. Jiang, A. Anderson, P. R. F. Barnes, L. Xiaoe, C. Law, B. C. O'Regan, J. Mater. Chem. A 2014, 2, 4751.\",,6.3,5.8,4.8,,,,,,,,,,,,\"OC, w-LED, 20 °C\",,1.3,5.5,1.77,,,,,,,,,Z907,,,\r\n\"S. M. Seo, C. K. Kim, H. K. Kim, J. Mater. Chem. A 2019, 7, 14743.\",,9.3,9.9,7.9,,,,,,,,,,,,\"OC, AM1.5G, 50 °C\",,1.9,9.2,1.78,,,,,,,,,N719,,,\r\n\"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\",,8.4,8.3, ,,,,,,,,,,,,\"OC, w-LED\",,1.7, ,1.83,,,,,,,,,MK2,,,\r\n\"J. Xia, Q. Wang, M. Chen, W. Li, J. Liu, J. Chen, H. Wu, S. Fan, Electrochim. Acta 2019, 307, 422.\",,8,8.3,8.3,,,,,,,,,,,,\"OC, AM1.5G\",,1.4,8.1,1.85,,,,,,,,,N719,,,\r\n\"J. Gao, M. Bhagavathi Achari, L. Kloo, Chem. Commun. 2014, 50, 6249.\",,5.8,6.5,5.9,,,,,,,,,,,,\"OC, AM1.5G, 60 °C\",,1.3,6.2,2.07,,,,,,,,,D35,,,\r\n\"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\",,24.4,24.3,19.3,,,,,,,,,1.26,,FSA:MA0.3FA0.7Pb0.5Sn0.5I3,\"MPP, encapsulation, air, 30–50% RH, AM1.5G, no UV-f, 54–60 °C\",,4.9,21.8,,1.82,,,,,,,,,,FA0.8Cs0.2Pb(I0.6Br0.4)3,\r\n\"Z. Yu, Z. Yang, Z. Ni, Y. Shao, B. Chen, Y. Lin, H. Wei, Z. J. Yu, Z. Holman, J. Huang, Nat. Energy 2020, 5, 657.\",,21.2,20.6,19.8,,,,,,,,,1.26,,Cs0.05MA0.45FA0.5Pb0.5Sn0.5I3,\"MPP-RL, encapsulation, air, AM1.5G, room T\",,4.2,20.7,,1.82,,,,,,,,,,Cs0.4FA0.6PbI1.95Br1.05,\r\n\"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\",,23.1,22.2,20.4,,,,,,,,,1.27,,(FASnI3)0.6(MAPbI3)0.4,\"MPP, AM1.5G\",,4.7,21.4,,1.72,,,,,,,,,,Cs0.05FA0.8MA0.15PbI2.55Br0.45,\r\n\"Z. Li, T. H. Kim, S. Y. Han, Y.-J. Yun, S. Jeong, B. Jo, S. A. Ok, W. Yim, S. H. Lee, K. Kim, S. Moon, J.-Y. Park, T. K. Ahn, H. Shin, J. Lee, H. J. Park, Adv. Energy Mater. 2020, 10, 1903085.\",,24.1,23.9,22.1,,,,,,,,,1.42,,GaAs,\"MPP, air 20–25% RH, AM1.5G, room T, UV-f\",,4.76,23.3,,1.85,,,,,,,,,,FA0.80MA0.04Cs0.16Pb(I0.50Br0.50)3,\r\n\"Q. Han, Y.-T. Hsieh, L. Meng, J.-L. Wu, P. Sun, E.-P. Yao, S.-Y. Chang, S.-H. Bae, T. Kato, V. Bermudez, Y. Yang, Science 2018, 361, 904.\",,22,19.9,18.4,,,,,,,,,1.1,,CIGS,\"MPP, air 20% RH, 30 °C\",,4.1,19.4,,1.65,,,,,,,,,,Cs0.09FA0.77MA0.14Pb(I0.86Br0.14)3,\r\n\"Y. Lei, Y. Li, C. Lu, Q. Yan, Y. Wu, F. Babbe, H. Gong, S. Zhang, J. Zhou, R. Wang, R. Zhang, Y. Chen, H. Tsai, Y. Gu, H. Hu, Y.-H. Lo, W. Nie, T. Lee, J. Luo, K. Yang, K.-I. Jang, S. Xu, Nature 2022, 608, 317.\",12.4,,,,,,,,,,MAPb0.5Sn0.5Br3:Bi3+:BA2MA4Sn5I16 ,,,,,,,,,1.12,,,,72.9,17.5,,,,,,,967\r\n\"X. Zhou, L. Zhang, J. Yu, D. Wang, C. Liu, S. Chen, Y. Li, Y. Li, M. Zhang, Y. Peng, Y. Tian, J. Huang, X. Wang, X. Guo, B. Xu, Adv. Mater. 2022, 34, 2205809.\",24.3,,,,,,,,,,FA0.7MA0.3Pb0.7Sn0.3I3/BTBTI:PCBM,,,,,,,,,1.18,,,,78,29.1,,,,,,,1070\r\n\"X. Zhou, L. Zhang, J. Yu, D. Wang, C. Liu, S. Chen, Y. Li, Y. Li, M. Zhang, Y. Peng, Y. Tian, J. Huang, X. Wang, X. Guo, B. Xu, Adv. Mater. 2022, 34, 2205809.\",23.4,,,,,,,,,,FA0.7MA0.3Pb0.7Sn0.3I3/BTBTI:PCBM,,,,,,,,,1.18,,,,75.8,28.9,,,,,,,1067\r\n\"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\",22.2,,,,,,,,,,FA0.7MA0.3Pb0.5Sn0.5I3,,,,,,,,,1.25,,,,80,33,,,,,,,841\r\n\"G. Kapil, T. Bessho, Y. Sanehira, S. R. Sahamir, M. Chen, A. K. Baranwal, D. Liu, Y. Sono, D. Hirotani, D. Nomura, K. Nishimura, M. A. Kamarudin, Q. Shen, H. Segawa, S. Hayase, ACS Energy Lett. 2022, 7, 966.\",23.3,,,,,,,,,,Cs0.025FA0.475MA0.5Pb0.5Sn0.5I2.925Br0.075,,,,,,,,,1.29,,,,80.8,32.8,,,,,,,880\r\n\"J. Sanchez-Diaz, R. S. Sánchez, S. Masi, M. Kreĉmarová, A. O. Alvarez, E. M. Barea, J. Rodriguez-Romero, V. S. Chirvony, J. F. Sánchez-Royo, J. P. Martinez-Pastor, I. Mora-Seró, Joule 2022, 6, 861.\",10.1,,,,,,,,,,FASnI3 + DipI + NaBH4,,,,,,,,,1.4,,,,69.6,22.1,,,,,,,655\r\n\"Z. Zhu, X. Jiang, D. Yu, N. Yu, Z. Ning, Q. Mi, ACS Energy Lett. 2022, 7, 2079.\",14.3,,,,,,,,,,FASnI3,,,,,,,,,1.42,,,,76.2,20.4,,,,,,,920\r\n\"Y. Su, J. Yang, G. Liu, W. Sheng, J. Zhang, Y. Zhong, L. Tan, Y. Chen, Adv. Funct. Mater. 2022, 32, 2109631.\",12.3,,,,,,,,,,EA0.098EDA0.01FA0.882SnI3,,,,,,,,,1.44,,,,75.3,21.7,,,,,,,750\r\n\"T. Wu, X. Liu, X. Luo, H. Segawa, G. Tong, Y. Zhang, L. K. Ono, Y. Qi, L. Han, Nano-Micro Lett. 2022, 14, 99.\",13.6,,,,,,,,,,FASnI3,,,,,,,,,1.45,,,,70.8,22.9,,,,,,,840\r\n\"Q. Jiang, J. Tong, Y. Xian, R. A. Kerner, S. P. Dunfield, C. Xiao, R. A. Scheidt, D. Kuciauskas, X. Wang, M. P. Hautzinger, R. Tirawat, M. C. Beard, D. P. Fenning, J. J. Berry, B. W. Larson, Y. Yan, K. Zhu, Nature 2022, 611, 278.\",25.3,,,,,,,,,,Cs0.05FA0.85MA0.05Rb0.05PbBr0.15I2.85,,,,,,,,,1.52,,,,83.9,26.2,,,,,,,1150\r\n\"Q. Jiang, J. Tong, Y. Xian, R. A. Kerner, S. P. Dunfield, C. Xiao, R. A. Scheidt, D. Kuciauskas, X. Wang, M. P. Hautzinger, R. Tirawat, M. C. Beard, D. P. Fenning, J. J. Berry, B. W. Larson, Y. Yan, K. Zhu, Nature 2022, 611, 278.\",24.1,,,,,,,,,,Cs0.05FA0.85MA0.05Rb0.05PbBr0.15I2.85,,,,,,,,,1.52,,,,81.4,25.4,,,,,,,1161\r\n\"Z. Xiong, X. Chen, B. Zhang, G. O. Odunmbaku, Z. Ou, B. Guo, K. Yang, Z. Kan, S. Lu, S. Chen, N. A. N. Ouedraogo, Y. Cho, C. Yang, J. Chen, K. Sun, Adv. Mater. 2022, 34, 2106118.\",24,,,,,,,,,,FAxMA1-xPbI3,,,,,,,,,1.53,,,,81.7,24.9,,,,,,,1180\r\n\"F. Zhang, Y. Park So, C. Yao, H. Lu, P. Dunfield Sean, C. Xiao, S. Uličná, X. Zhao, L. Du Hill, X. Chen, X. Wang, E. Mundt Laura, H. Stone Kevin, T. Schelhas Laura, G. Teeter, S. Parkin, L. Ratcliff Erin, Y.-L. Loo, J. Berry Joseph, C. Beard Matthew, Y. Yan, W. Larson Bryon, K. Zhu, Science 2022, 375, 71.\",24.5,,,,,,,,,,FA0.97MA0.03PbI2.91Br0.09,,,,,,,,,1.53,,,,83.8,25.3,,,,,,,1158\r\n\"M. Kim, J. Jeong, H. Lu, K. Lee Tae, T. Eickemeyer Felix, Y. Liu, W. Choi In, J. Choi Seung, Y. Jo, H.-B. Kim, S.-I. Mo, Y.-K. Kim, H. Lee, G. An Na, S. Cho, R. Tress Wolfgang, M. Zakeeruddin Shaik, A. Hagfeldt, Y. Kim Jin, M. Grätzel, S. Kim Dong, Science 2022, 375, 302.\",25.4,,,,,,,,,,FAPbI3,,,,,,,,,1.53,,,,81.9,26.4,,,,,,,1174\r\n\"Y. Zhao, F. Ma, Z. Qu, S. Yu, T. Shen, H.-X. Deng, X. Chu, X. Peng, Y. Yuan, X. Zhang, J. You, Science 2022, 377, 531.\",25.6,,,,,,,,,,FAPbI3: (PbI2)2RbCl,,,,,,,,,1.54,,,,82.6,26.2,,,,,,,1182\r\n\"Y. Li, Z. Chen, B. Yu, S. Tan, Y. Cui, H. Wu, Y. Luo, J. Shi, D. Li, Q. Meng, Joule 2022, 6, 676.\",24.3,,,,,,,,,,Cs0.03FA0.97 Pb Br0.09I2.91,,,,,,,,,1.54,,,,82.6,25.7,,,,,,,1141\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\",25.7,,,,,,,,,, ,,,,,,,,,1.54,,,,84.5,25.8,,,,,,,1179\r\n\"S. Tan, T. Huang, I. Yavuz, R. Wang, T. W. Yoon, M. Xu, Q. Xing, K. Park, D.-K. Lee, C.-H. Chen, R. Zheng, T. Yoon, Y. Zhao, H.-C. Wang, D. Meng, J. Xue, Y. J. Song, X. Pan, N.-G. Park, J.-W. Lee, Y. Yang, Nature 2022, 605, 268.\",24.1,,,,,,,,,,FA0.95MA0.05PbBr0.15I2.85,,,,,,,,,1.55,,,,82.3,25.3,,,,,,,1158\r\n\"Z. Shen, Q. Han, X. Luo, Y. Shen, T. Wang, C. Zhang, Y. Wang, H. Chen, X. Yang, Y. Zhang, L. Han, Energy Environ. Sci. 2022, 15, 1078.\",25.1,,,,,,,,,,FA0.995MA0.005PbBr0.015I0.985,,,,,,,,,1.56,,,,84.4,24.9,,,,,,,1195\r\n\"X. Li, W. Zhang, X. Guo, C. Lu, J. Wei, J. Fang, Science 2022, 375, 434.\",23,,,,,,,,,,FA0.95MA0.05PbBr0.15I2.85,,,,,,,,,1.57,,,,79.9,25.1,,,,,,,1147\r\n\"X. Wang, W. Sun, Y. Tu, Q. Xiong, G. Li, Z. Song, Y. Wang, Y. Du, Q. Chen, C. Deng, Z. Lan, P. Gao, J. Wu, Chem. Eng. J. 2022, 446, 137416.\",23.4,,,,,,,,,,Cs0.05FA0.75MA0.15Rb0.05PbBr0.15I2.85,,,,,,,,,1.57,,,,80.6,25.2,,,,,,,1153\r\n\"J. Peng, F. Kremer, D. Walter, Y. Wu, Y. Ji, J. Xiang, W. Liu, T. Duong, H. Shen, T. Lu, F. Brink, D. Zhong, L. Li, O. Lee Cheong Lem, Y. Liu, K. J. Weber, T. P. White, K. R. Catchpole, Nature 2022, 601, 573.\",22.9,,,,,,,,,,Cs0.05FA0.9MA0.05PbBr0.26I2.74,,,,,,,,,1.58,,,,80,23.4,,,,,,,1173\r\n\"Y. Zhang, N.-G. Park, ACS Energy Lett. 2022, 7, 757.\",21.9,,,,,,,,,,GA(MA)5Pb5I16,,,,,,,,,1.6,,,,80.6,22.8,,,,,,,1192\r\n\"S. Wang, Y. Li, J. Yang, T. Wang, B. Yang, Q. Cao, X. Pu, L. Etgar, J. Han, J. Zhao, X. Li, A. Hagfeldt, Angew. Chem., Int. Ed. 2022, 61, 202116534.\",22.4,,,,,,,,,,Cs0.05MA0.1425FA0.8075PbBr0.45I2.55,,,,,,,,,1.64,,,,83.8,23.7,,,,,,,1130\r\n\"G. Yang, Z. Ni, Z. J. Yu, B. W. Larson, Z. Yu, B. Chen, A. Alasfour, X. Xiao, J. M. Luther, Z. C. Holman, J. Huang, Nat. Photonics 2022, 16, 588.\",21.9,,,,,,,,,,Cs0.1FA0.2MA0.7PbBr0.45I0.2.55,,,,,,,,,1.65,,,,84,21.2,,,,,,,1230\r\n\"S. Tan, B. Yu, Y. Cui, F. Meng, C. Huang, Y. Li, Z. Chen, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Angew. Chem., Int. Ed. 2022, 61, 202201300.\",20.2,,,,,,,,,,CsPbI3,,,,,,,,,1.7,,,,82.5,20.8,,,,,,,1176\r\n\"S. Tan, B. Yu, Y. Cui, F. Meng, C. Huang, Y. Li, Z. Chen, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Angew. Chem., Int. Ed. 2022, 61, 202201300.\",20.1,,,,,,,,,,CsPbI3,,,,,,,,,1.7,,,,82.8,20.6,,,,,,,1177\r\n\"M. A. Mahmud, J. Zheng, S. Tang, G. Wang, J. Bing, A. D. Bui, J. Qu, L. Yang, C. Liao, H. Chen, S. P. Bremner, H. T. Nguyen, J. Cairney, A. W. Y. Ho-Baillie, Adv. Energy Mater. 2022, 12, 2201672.\",20.2,,,,,,,,,,Cs0.2FA0.8PbBr0.9I2.1,,,,,,,,,1.74,,,,86.5,19.3,,,,,,,1210\r\n\"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\",17.3,,,,,,,,,,Cs0.2FA0.8PbBr1.14I1.86,,,,,,,,,1.78,,,,81.2,17.4,,,,,,,1227\r\n\"J. Wen, Y. Zhao, Z. Liu, H. Gao, R. Lin, S. Wan, C. Ji, K. Xiao, Y. Gao, Y. Tian, J. Xie, C. J. Brabec, H. Tan, Adv. Mater. 2022, 34, 2110356.\",17.7,,,,,,,,,,Cs0.4DMA0.1FA0.5PbBr0.71Cl0.15I2.14,,,,,,,,,1.79,,,,81.1,17.4,,,,,,,1255\r\n\"K. Xiao, Y.-H. Lin, M. Zhang, R. D. J. Oliver, X. Wang, Z. Liu, X. Luo, J. Li, D. Lai, H. Luo, R. Lin, J. Xu, Y. Hou, H. J. Snaith, H. Tan, Science 2022, 376, 762.\",17.2,,,,,,,,,,Cs0.35FA0.65PbBr1.2I1.8,,,,,,,,,1.82,,,,80.9,16.8,,,,,,,1266\r\n\"S. Qin, C. Lu, Z. Jia, Y. Wang, S. Li, W. Lai, P. Shi, R. Wang, C. Zhu, J. Du, J. Zhang, L. Meng, Y. Li, Adv. Mater. 2022, 34, 2108829.\",16.9,,,,,,,,,,FA0.6MA0.4PbBr1.2I1.8,,,,,,,,,1.83,,,,80.7,16.9,,,,,,,1240\r\n\"Z. Guo, A. K. Jena, I. Takei, M. Ikegami, A. Ishii, Y. Numata, N. Shibayama, T. Miyasaka, Adv. Funct. Mater. 2021, 31, 2103614.\",17.4,,,,,,,,,,CsPbBrI2,,,,,,,,,1.88,,,,81.4,15,,,,,,,1420\r\n\"W. Chen, D. Li, X. Chen, H. Chen, S. Liu, H. Yang, X. Li, Y. Shen, X. Ou, Y. Yang, L. Jiang, Y. Li, Y. Li, Adv. Funct. Mater. 2022, 32, 2109321.\",13.4,,,,,,,,,,CsPbI1.8Br1.2,,,,,,,,,1.94,,,,76,14.2,,,,,,,1240\r\n\"H. Xu, Z. Liang, J. Ye, S. Xu, Z. Wang, L. Zhu, X. Chen, Z. Xiao, X. Pan, G. Liu, Chem. Eng. J. 2022, 437, 135181.\",8.9,,,,,,,,,,FAPbBr3,,,,,,,,,2.2,,,,70.6,7.7,,,,,,,1639\r\n\"X. Li, Y. Tan, H. Lai, S. Li, Y. Chen, S. Li, P. Xu, J. Yang, ACS Appl. Mater. Interfaces 2019, 11, 29746.\",10.5,,,,,,,,,,CsPbBr3,,,,,,,,,2.28,,,,83,8.3,,,,,,,1520\r\n\"H. Zhu, L. Pan, F. T. Eickemeyer, M. A. Hope, O. Ouellette, A. Q. M. Alanazi, J. Gao, T. P. Baumeler, X. Li, S. Wang, S. M. Zakeeruddin, Y. Liu, L. Emsley, M. Grätzel, ACS Energy Lett. 2022, 7, 1112.\",10.2,,,,,,,,,,MAPbBr3,,,,,,,,,2.29,,,,71.1,8.7,,,,,,,1650\r\n\"X. Yao, B. He, J. Zhu, J. Ti, L. Cui, R. Tui, M. Wei, H. Chen, J. Duan, Y. Duan, Q. Tang, Nano Energy 2022, 96, 107138.\",10.7,,,,,,,,,,CsPbBr3,,,,,,,,,2.34,,,,84.1,7.8,,,,,,,1635\r\n\"J. Zhu, Y. Liu, B. He, W. Zhang, L. Cui, S. Wang, H. Chen, Y. Duan, Q. Tang, Chem. Eng. J. 2022, 428, 131950.\",10.2,,,,,,,,,,CsPbBr3,,,,,,,,,2.35,,,,81,7.8,,,,,,,1611\r\n\"H. Yuan, Y. Zhao, J. Duan, Y. Wang, X. Yang, Q. Tang, J. Mater. Chem. A 2018, 6, 24324.\",10.3,,,,,,,,,,CsPb0.97Tb0.03Br3,,,,,,,,,2.36,,,,79.6,8.2,,,,,,,1570\r\n\"B. Li, X. Wu, S. Zhang, Z. Li, D. Gao, X. Chen, S. Xiao, C.-C. Chueh, A. K. Y. Jen, Z. Zhu, Chem. Eng. J. 2022, 446, 137144.\",3.3,,,,,,,,,,Cs2AgBiBr6,,,,,,,,,2.47,,,,77.5,3.3,,,,,,,1278\r\n\"W. Liu, S. Sun, S. Xu, H. Zhang, Y. Zheng, Z. Wei, X. Zhu, Adv. Mater. 2022, 34, 2200337.\",13.4,,,,,,,BTB7-Th:ATT-9,,,,,,,,,,,,1.22,,,,67.1,30,,,,,,,663\r\n\"Z. Liu, H.-E. Wang, Sustainable Energy Fuels 2022, 6, 744.\",13,,,,,,,BTR:Y6:bisPC71BM,,,,,,,,,,,,1.32,,,,70.1,20.2,,,,,,,916\r\n\"Z. Liu, N. Wang, Sol. Energy 2021, 214, 110.\",13.9,,,,,,,BTR:MeIC:Y11,,,,,,,,,,,,1.33,,,,71.4,22.4,,,,,,,865\r\n\"Y. Pan, X. Zheng, J. Guo, Z. Chen, S. Li, C. He, S. Ye, X. Xia, S. Wang, X. Lu, H. Zhu, J. Min, L. Zuo, M. Shi, H. Chen, Adv. Funct. Mater. 2022, 32, 2108614.\",18.2,,,,,,,PM6:BTP-T-3Cl:BTP-4Cl-BO,,,,,,,,,,,,1.38,,,,77.6,27.4,,,,,,,857\r\n\"L. Zhan, S. Li, Y. Li, R. Sun, J. Min, Z. Bi, W. Ma, Z. Chen, G. Zhou, H. Zhu, M. Shi, L. Zuo, H. Chen, Joule 2022, 6, 662.\",18.8,,,,,,,PM6:BTP-eC9:BTP-S9,,,,,,,,,,,,1.38,,,,79.4,27.5,,,,,,,861\r\n\"Y. Cai, Y. Li, R. Wang, H. Wu, Z. Chen, J. Zhang, Z. Ma, X. Hao, Y. Zhao, C. Zhang, F. Huang, Y. Sun, Adv. Mater. 2021, 33, 2101733.\",18.7,,,,,,,PM6:BTP-eC9:L8-BO-F,,,,,,,,,,,,1.38,,,,80,27.4,,,,,,,853\r\n\"Y. Cai, Y. Li, R. Wang, H. Wu, Z. Chen, J. Zhang, Z. Ma, X. Hao, Y. Zhao, C. Zhang, F. Huang, Y. Sun, Adv. Mater. 2021, 33, 2101733.\",18.2,,,,,,,PM6:BTP-eC9:L8-BO-F,,,,,,,,,,,,1.38,,,,78.8,27.3,,,,,,,847\r\n\"L. Zhan, S. Li, Y. Li, R. Sun, J. Min, Z. Bi, W. Ma, Z. Chen, G. Zhou, H. Zhu, M. Shi, L. Zuo, H. Chen, Joule 2022, 6, 662.\",18.7,,,,,,,PM6:BTP-eC9:BTP-S9,,,,,,,,,,,,1.38,,,,79.3,27.4,,,,,,,862\r\n\"D. Wang, G. Zhou, Y. Li, K. Yan, L. Zhan, H. Zhu, X. Lu, H. Chen, C.-Z. Li, Adv. Funct. Mater. 2022, 32, 2107827.\",18.1,,,,,,,PM6:Y6-1O:BO-4Cl,,,,,,,,,,,,1.39,,,,77.5,27.5,,,,,,,848\r\n\"D. Wang, G. Zhou, Y. Li, K. Yan, L. Zhan, H. Zhu, X. Lu, H. Chen, C.-Z. Li, Adv. Funct. Mater. 2022, 32, 2107827.\",18.5,,,,,,,PM6:Y6-1O:BO-4Cl,,,,,,,,,,,,1.39,,,,78.9,27.5,,,,,,,855\r\n\"T. Zhang, C. An, Y. Cui, J. Zhang, P. Bi, C. Yang, S. Zhang, J. Hou, Adv. Mater. 2022, 34, 2105803.\",18.4,,,,,,,PB2:PBDB-TF:BTP-eC9,,,,,,,,,,,,1.39,,,,79.7,26.9,,,,,,,858\r\n\"L. Zuo, S. B. Jo, Y. Li, Y. Meng, R. J. Stoddard, Y. Liu, F. Lin, X. Shi, F. Liu, H. W. Hillhouse, D. S. Ginger, H. Chen, A. K. Y. Jen, Nat. Nanotechnol. 2022, 17, 53.\",18.3,,,,,,,PM6:BTP-eC11:BTP-S2,,,,,,,,,,,,1.39,,,,78.9,26.6,,,,,,,872\r\n\"X. Duan, W. Song, J. Qiao, X. Li, Y. Cai, H. Wu, J. Zhang, X. Hao, Z. Tang, Z. Ge, F. Huang, Y. Sun, Energy Environ. Sci. 2022, 15, 1563.\",18.2,,,,,,,PM6:BTP-eC9:ZY-4Cl,,,,,,,,,,,,1.39,,,,77.9,27.1,,,,,,,863\r\n\"X. Duan, W. Song, J. Qiao, X. Li, Y. Cai, H. Wu, J. Zhang, X. Hao, Z. Tang, Z. Ge, F. Huang, Y. Sun, Energy Environ. Sci. 2022, 15, 1563.\",18.7,,,,,,,PM6:BTP-eC9:ZY-4Cl,,,,,,,,,,,,1.39,,,,79,27.4,,,,,,,863\r\n\"S. Guan, Y. Li, K. Yan, W. Fu, L. Zuo, H. Chen, Adv. Mater. 2022, 34, 2205844.\",19.1,,,,,,,PBDB-TF:L8-BO:BTP-eC9,,,,,,,,,,,,1.4,,,,79.9,27.5,,,,,,,869\r\n\"S. Guan, Y. Li, K. Yan, W. Fu, L. Zuo, H. Chen, Adv. Mater. 2022, 34, 2205844.\",19.4,,,,,,,PBDB-TF:L8-BO:BTP-eC9,,,,,,,,,,,,1.4,,,,81.2,27.6,,,,,,,863\r\n\"C. He, Z. Bi, Z. Chen, J. Guo, X. Xia, X. Lu, J. Min, H. Zhu, W. Ma, L. Zuo, H. Chen, Adv. Funct. Mater. 2022, 32, 2112511.\",18.1,,,,,,,PM6:AC9,,,,,,,,,,,,1.4,,,,78,26.8,,,,,,,867\r\n\"W. Feng, S. Wu, H. Chen, L. Meng, F. Huang, H. Liang, J. Zhang, Z. Wei, X. Wan, C. Li, Z. Yao, Y. Chen, Adv. Energy Mater. 2022, 12, 2104060.\",18.1,,,,,,,PM6:CNS-6-8:Y6:PC71BM,,,,,,,,,,,,1.4,,,,78.8,26.4,,,,,,,868\r\n\"C. He, Z. Bi, Z. Chen, J. Guo, X. Xia, X. Lu, J. Min, H. Zhu, W. Ma, L. Zuo, H. Chen, Adv. Funct. Mater. 2022, 32, 2112511.\",18.4,,,,,,,PM6:AC9,,,,,,,,,,,,1.4,,,,79.1,26.8,,,,,,,871\r\n\"B. Fan, W. Gao, X. Wu, X. Xia, Y. Wu, F. R. Lin, Q. Fan, X. Lu, W. J. Li, W. Ma, A. K. Y. Jen, Nat. Commun. 2022, 13, 5946.\",18.3,,,,,,,PTzBI-dF:BTP-TBr,,,,,,,,,,,,1.4,,,,78.8,27.5,,,,,,,845\r\n\"R. Yu, X. Wei, G. Wu, T. Zhang, Y. Gong, B. Zhao, J. Hou, C. Yang, Z. Tan, Energy Environ. Sci. 2022, 15, 822.\",18.1,,,,,,,PM6:PB2F:BTP-eC9,,,,,,,,,,,,1.41,,,,79.4,26.5,,,,,,,860\r\n\"Y. Cui, Y. Xu, H. Yao, P. Bi, L. Hong, J. Zhang, Y. Zu, T. Zhang, J. Qin, J. Ren, Z. Chen, C. He, X. Hao, Z. Wei, J. Hou, Adv. Mater. 2021, 33, 2102420.\",19,,,,,,,PBQx-TF:eC9-2Cl:F-BTA3,,,,,,,,,,,,1.41,,,,81,26.7,,,,,,,879\r\n\"Y. Cui, Y. Xu, H. Yao, P. Bi, L. Hong, J. Zhang, Y. Zu, T. Zhang, J. Qin, J. Ren, Z. Chen, C. He, X. Hao, Z. Wei, J. Hou, Adv. Mater. 2021, 33, 2102420.\",18.7,,,,,,,PBQx-TF:eC9-2Cl:F-BTA3,,,,,,,,,,,,1.41,,,,79.4,26.8,,,,,,,878\r\n\"J. Zhang, F. Bai, I. Angunawela, X. Xu, S. Luo, C. Li, G. Chai, H. Yu, Y. Chen, H. Hu, Z. Ma, H. Ade, H. Yan, Adv. Energy Mater. 2021, 11, 2102596.\",18.2,,,,,,,PBDB-T-2F:BTP-4F-P2EH,,,,,,,,,,,,1.43,,,,80.1,25.9,,,,,,,880\r\n\"J. Song, L. Zhu, C. Li, J. Xu, H. Wu, X. Zhang, Y. Zhang, Z. Tang, F. Liu, Y. Sun, Matter 2021, 4, 2542.\",18.6,,,,,,,PM6:L8-BO,,,,,,,,,,,,1.44,,,,80,26,,,,,,,893\r\n\"J. Song, L. Zhu, C. Li, J. Xu, H. Wu, X. Zhang, Y. Zhang, Z. Tang, F. Liu, Y. Sun, Matter 2021, 4, 2542.\",18.2,,,,,,,PM6:L8-BO,,,,,,,,,,,,1.44,,,,79,26.1,,,,,,,883\r\n\"L. Zhu, M. Zhang, J. Xu, C. Li, J. Yan, G. Zhou, W. Zhong, T. Hao, J. Song, X. Xue, Z. Zhou, R. Zeng, H. Zhu, C.-C. Chen, R. C. I. MacKenzie, Y. Zou, J. Nelson, Y. Zhang, Y. Sun, F. Liu, Nat. Mater. 2022, 21, 656.\",19.6,,,,,,,PM6:D18:L8-BO,,,,,,,,,,,,1.45,,,,81.9,26.7,,,,,,,896\r\n\"Y. Wei, Z. Chen, G. Lu, N. Yu, C. Li, J. Gao, X. Gu, X. Hao, G. Lu, Z. Tang, J. Zhang, Z. Wei, X. Zhang, H. Huang, Adv. Mater. 2022, 34, 2204718.\",19.1,,,,,,,D18:L8-BO,,,,,,,,,,,,1.45,,,,77.3,26.9,,,,,,,918\r\n\"L. Zhu, M. Zhang, J. Xu, C. Li, J. Yan, G. Zhou, W. Zhong, T. Hao, J. Song, X. Xue, Z. Zhou, R. Zeng, H. Zhu, C.-C. Chen, R. C. I. MacKenzie, Y. Zou, J. Nelson, Y. Zhang, Y. Sun, F. Liu, Nat. Mater. 2022, 21, 656.\",19.2,,,,,,,PM6:D18:L8-BO,,,,,,,,,,,,1.45,,,,80.7,26.7,,,,,,,891\r\n\"Y. Li, J. Song, Y. Dong, H. Jin, J. Xin, S. Wang, Y. Cai, L. Jiang, W. Ma, Z. Tang, Y. Sun, Adv. Mater. 2022, 34, 2110155.\",16.8,,,,,,,PM6:PY-DT,,,,,,,,,,,,1.46,,,,74.4,23.7,,,,,,,949\r\n\"S. Mathew, A. Yella, P. Gao, R. Humphry-Baker, B. F. E. Curchod, N. Ashari-Astani, I. Tavernelli, U. Rothlisberger, M. K. Nazeeruddin, M. Grätzel, Nat. Chem. 2014, 6, 242.\",13,,,,,,,,,,,,,,,,,,,1.66,,,,78,18.1,,,,SM315,,,910\r\n\"S. Mathew, A. Yella, P. Gao, R. Humphry-Baker, B. F. E. Curchod, N. Ashari-Astani, I. Tavernelli, U. Rothlisberger, M. K. Nazeeruddin, M. Grätzel, Nat. Chem. 2014, 6, 242.\",12,,,,,,,,,,,,,,,,,,,1.76,,,,79,15.9,,,,SM371,,,960\r\n\"P.-H. Chang, M. C. Sil, K. S. K. Reddy, C.-H. Lin, C.-M. Chen, ACS Appl. Mater. Interfaces 2022, 14, 25466.\",9.9,,,,,,,,,,,,,,,,,,,1.79,,,,70.5,19,,,,PI-COF:N719,,,740\r\n\"A. K. Bharwal, L. Manceriu, C. Olivier, A. Mahmoud, C. Iojoiu, T. Toupance, C. M. Ruiz, M. Pasquinelli, D. Duché, J.-J. Simon, C. Henrist, F. Alloin, Chem. Eng. J. 2022, 446, 136777.\",8.5,,,,,,,,,,,,,,,,,,,1.81,,,,62.6,19.4,,,,N719,,,700\r\n\"Y. Ren, D. Zhang, J. Suo, Y. Cao, F. T. Eickemeyer, N. Vlachopoulos, S. M. Zakeeruddin, A. Hagfeldt, M. Grätzel, Nature 2022, https://doi.org/10.1038/s41586-022-05460-z.\",15.2,,,,,,,,,,,,,,,,,,,1.83,,,,79.4,18,,,,SL9 + SL10/BPHA,,,1063\r\n\"C. Liao, H. Wu, H. Tang, L. Wang, D. Cao, Sol. Energy 2022, 240, 399.\",4.1,,,,,,,,,,,,,,,,,,,2.15,,,,73.6,8.76,,,,PS1,,,640\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\",13.6,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.1,,,,69.9,36.2,,,,,,,538\r\n\"J. Wang, J. Zhou, X. Xu, F. Meng, C. Xiang, L. Lou, K. Yin, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, H. Xin, Q. Meng, Adv. Mater. 2022, 34, 2202858.\",13.1,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.11,,,,70,34.3,,,,,,,547\r\n\"J. Wang, J. Zhou, X. Xu, F. Meng, C. Xiang, L. Lou, K. Yin, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, H. Xin, Q. Meng, Adv. Mater. 2022, 34, 2202858.\",12.8,,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,1.11,,,,68.9,35.3,,,,,,,526\r\n\"R. Tang, S. Chen, Z.-H. Zheng, Z.-H. Su, J.-T. Luo, P. Fan, X.-H. Zhang, J. Tang, G.-X. Liang, Adv. Mater. 2022, 34, 2109078.\",8.6,,,,,,,,,Sb2Se3,,,,,,,,,,1.33,,,,59.8,27.8,,,,,,,520\r\n\"Y. Wang, L. Peng, Z. Wang, G. Konstantatos, Adv. Energy Mater. 2022, 12, 2200700.\",7.1,,,,,,,,,AgBiS2,,,,,,,,,,1.37,,,,60,24.7,,,,,,,480\r\n\"Y. Wang, S. R. Kavanagh, I. Burgués-Ceballos, A. Walsh, D. O. Scanlon, G. Konstantatos, Nat. Photonics 2022, 16, 235.\",8.9,,,,,,,,,AgBiS2,,,,,,,,,,1.39,,,,68.5,26.8,,,,,,,482\r\n\"Y. Wang, S. R. Kavanagh, I. Burgués-Ceballos, A. Walsh, D. O. Scanlon, G. Konstantatos, Nat. Photonics 2022, 16, 235.\",9.2,,,,,,,,,AgBiS2,,,,,,,,,,1.39,,,,68.4,27.1,,,,,,,495\r\n\"R. Tang, X. Wang, W. Lian, J. Huang, Q. Wei, M. Huang, Y. Yin, C. Jiang, S. Yang, G. Xing, S. Chen, C. Zhu, X. Hao, M. A. Green, T. Chen, Nat. Energy 2020, 5, 587.\",10,,,,,,,,,\"Sb2(S,Se)3\",,,,,,,,,,1.5,,,,63.3,24.1,,,,,,,655\r\n\"Y. Zhao, S. Wang, C. Jiang, C. Li, P. Xiao, R. Tang, J. Gong, G. Chen, T. Chen, J. Li, X. Xiao, Adv. Energy Mater. 2022, 12, 2103015.\",10.7,,,,,,,,,\"Sb2(S,Se)3\",,,,,,,,,,1.54,,,,66.8,23.7,,,,,,,673\r\n\"C. Jiang, J. Zhou, R. Tang, W. Lian, X. Wang, X. Lei, H. Zeng, C. Zhu, W. Tang, T. Chen, Energy Environ. Sci. 2021, 14, 359.\",9.7,,,,,,,,,\"Sb2(S,Se)3\",,,,,,,,,,1.54,,,,65.5,23.2,,,,,,,638\r\n\"X. Wang, R. Tang, C. Jiang, W. Lian, H. Ju, G. Jiang, Z. Li, C. Zhu, T. Chen, Adv. Energy Mater. 2020, 10, 2002341.\",10.5,,,,,,,,,\"Sb2(S,Se)3\",,,,,,,,,,1.55,,,,66.3,23.8,,,,,,,664\r\n\"S. Wang, Y. Zhao, B. Che, C. Li, X. Chen, R. Tang, J. Gong, X. Wang, G. Chen, T. Chen, J. Li, X. Xiao, Adv. Mater. 2022, 34, 2206242.\",8,,,,,,,,,Sb2S3,,,,,,,,,,1.73,,,,17.4,60.5,,,,,,,757\r\n\"Z. Sun, M. Liu, Y. Zhou, Q. Wang, Y. Yang, Y. Zhou, F. Liu, Sol. Energy Mater. Sol. Cells 2022, 235, 111453.\",20,,,,,,,,,Si,,,,,,,,,,1.18,,,,69.7,40.7,,,,,,,706\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\",29.8,,,,,,,,,,,,,,Si,,,,,,,1.11,1.69,79.8,19.5,, ,,,,,1190\r\n\"L. Mao, T. Yang, H. Zhang, J. Shi, Y. Hu, P. Zeng, F. Li, J. Gong, X. Fang, Y. Sun, X. Liu, J. Du, A. Han, L. Zhang, W. Liu, F. Meng, X. Cui, Z. Liu, M. Liu, Adv. Mater. 2022, 34, 2206193.\",28.3,,,,,,,,,,,,,,Si,,,,,,,1.13,1.67,79.6,20.1,,FAMAPb(BrClI)3,,,,,1776\r\n\"Y. Wu, P. Zheng, J. Peng, M. Xu, Y. Chen, S. Surve, T. Lu, A. D. Bui, N. Li, W. Liang, L. Duan, B. Li, H. Shen, T. Duong, J. Yang, X. Zhang, Y. Liu, H. Jin, Q. Chen, T. White, K. Catchpole, H. Zhou, K. Weber, Adv. Energy Mater. 2022, 12, 2200821.\",27.5,,,,,,,,,,,,,,Si,,,,,,,1.14,1.68,78.9,19.6,,Cs0.22FA0.78PbBr0.45Cl0.09I2.55,,,,,1779\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\",26.8,,,,,,,,,,,,,,Si,,,,,,,1.14,1.69,79.4,17.8,, ,,,,,1891\r\n\"K. Liu, B. Chen, Z. J. Yu, Y. Wu, Z. Huang, X. Jia, C. Li, D. Spronk, Z. Wang, Z. Wang, S. Qu, Z. C. Holman, J. Huang, J. Mater. Chem. A 2022, 10, 1343.\",26,,,,,,,,,,,,,,Si,,,,,,,1.14,1.69,80.2,18.2,,Cs0.15FA0.7055MA0.1445PbBr0.6I2.4,,,,,1780\r\n\"M. A. Ruiz-Preciado, F. Gota, P. Fassl, I. M. Hossain, R. Singh, F. Laufer, F. Schackmar, T. Feeney, A. Farag, I. Allegro, H. Hu, S. Gharibzadeh, B. A. Nejand, V. S. Gevaerts, M. Simor, P. J. Bolt, U. W. Paetzold, ACS Energy Lett. 2022, 7, 2273.\",24.3,,,,,,,,,,,,,,CuInSe2,,,,,,,1.01,1.61,73.6,21,,Cs0.05FA0.85MA0.1PbI2.7Br0.3,,,,,1570\r\n\"M. A. Ruiz-Preciado, F. Gota, P. Fassl, I. M. Hossain, R. Singh, F. Laufer, F. Schackmar, T. Feeney, A. Farag, I. Allegro, H. Hu, S. Gharibzadeh, B. A. Nejand, V. S. Gevaerts, M. Simor, P. J. Bolt, U. W. Paetzold, ACS Energy Lett. 2022, 7, 2273.\",23.5,,,,,,,,,,,,,,CuInSe2,,,,,,,1.01,1.61,75.5,19.4,,Cs0.05FA0.85MA0.1PbI2.7Br0.3,,,,,1590\r\n\"M. Jošt, E. Köhnen, A. Al-Ashouri, T. Bertram, Š. Tomšič, A. Magomedov, E. Kasparavicius, T. Kodalle, B. Lipovšek, V. Getautis, R. Schlatmann, C. A. Kaufmann, S. Albrecht, M. Topič, ACS Energy Lett. 2022, 7, 1298.\",24.2,,,,,,,,,,,,,,CIGS,,,,,,,1.11,1.68,71.2,18.8,,Cs0.05FA0.7315MA0.2185PbBr0.69I2.31,,,,,1770\r\n\"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\",26.3 (26.4) ,,,,,,,,,,,,,,Cs0.2FA0.8 Pb Br1.14I1.86,,,,,,,1.25,1.8,78.1,16.5,,FA0.7MA0.3Pb0.5Sn0.5I3,,,,,2044\r\n\"K. Datta, J. Wang, D. Zhang, V. Zardetto, W. H. M. Remmerswaal, C. H. L. Weijtens, M. M. Wienk, R. A. J. Janssen, Adv. Mater. 2022, 34, 2110053.\",23.1,,,,,,,,,,,,,,FA0.66MA0.34Pb0.5Sn0.5I3,,,,,,,1.26,1.79,75,15.8,,Cs0.05(FAMA0.95)K0.05Pb(BrI)3,,,,,1950\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\",28,,,,,,,,,,,,,, ,,,,,,,1.26,1.8,80.2,16.42,, ,,,,,2125\r\n\"J. Wen, Y. Zhao, Z. Liu, H. Gao, R. Lin, S. Wan, C. Ji, K. Xiao, Y. Gao, Y. Tian, J. Xie, C. J. Brabec, H. Tan, Adv. Mater. 2022, 34, 2110356.\",26.2,,,,,,,,,,,,,,FA0.7MA0.3Pb0.5Sn0.5I3,,,,,,,1.26,1.8,80.1,16,,Cs0.4DMA0.1FA0.5PbBr0.71Cl0.15I2.14,,,,,2040\r\n\"H. Gao, Q. Lu, K. Xiao, Q. Han, R. Lin, Z. Liu, H. Li, L. Li, X. Luo, Y. Gao, Y. Wang, J. Wen, Z. Zou, Y. Zhou, H. Tan, Sol. RRL 2021, 5, 2100814.\",23.2,,,,,,,,,,,,,,Cs0.2FA0.8Pb0.5Sn0.5I3,,,,,,,1.27,1.82,79.8,15.4,,Cs0.2FA0.8PbBr1.2I1.8,,,,,1890\r\n\"S. Qin, C. Lu, Z. Jia, Y. Wang, S. Li, W. Lai, P. Shi, R. Wang, C. Zhu, J. Du, J. Zhang, L. Meng, Y. Li, Adv. Mater. 2022, 34, 2108829.\",21.7,,,,,,,,,,,,,,PTB7-Th:BTPV-4Cl-eC9,,,,,,,1.21,1.83,73.5,15.7,,FA0.6MA0.4PbBr1.2I1.8,,,,,1880\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\",23.4,,,,,,,,,,,,,, ,,,,,,,1.38,1.88,75.2,14.6,, ,,,,,2136\r\n\"J. Zheng, G. Wang, W. Duan, M. A. Mahmud, H. Yi, C. Xu, A. Lambertz, S. Bremner, K. Ding, S. Huang, A. W. Y. Ho-Baillie, ACS Energy Lett. 2022, 7, 3003.\",20.1,,,,,,,,,,,,,,Si,,,,,,,1.13,\"1.54, 1.91\",86,8.5,,\"Cs0.1FA0.9PbI3, Cs0.2FA0.8PbBr1.65I1.35\",,,,,2740\r\n\"J. Wang, V. Zardetto, K. Datta, D. Zhang, M. M. Wienk, R. A. J. Janssen, Nat. Commun. 2020, 11, 5254.\",16.8,,,,,,,,,,,,,,FA0.66MA0.34Pb0.5Sn0.5I3,,,,,,,1.23,\"1.57, 1.78\",81,7.4,,\"FA0.66MA0.34 Pb Br0.15I2.85, Cs0.1FA0.594MA0.306PbBrI2\",,,,,2780\r\n\"K. Xiao, J. Wen, Q. Han, R. Lin, Y. Gao, S. Gu, Y. Zang, Y. Nie, J. Zhu, J. Xu, H. Tan, ACS Energy Lett. 2020, 5, 2819.\",19.9,,,,,,,,,,,,,,FA0.7MA0.3Pb0.5Sn0.5I3,,,,,,,1.26,\"1.65, 2.06\",80.7,8.8,,\"Cs0.05FA0.95PbBr0.45 I2.55, Cs0.2FA0.8PbBr2.1I0.9\",,,,,2793\r\n\"Y. Huang, L. Meng, H. Liang, M. Li, H. Chen, C. Jiang, K. Zhang, F. Huang, Z. Yao, C. Li, X. Wan, Y. Chen, J. Mater. Chem. A 2022, 10, 11238.\",18.7,,,,,,,,,,,,,PM6:CH1007:PC71BM,,,,,,,1.73,1.36,,70.9,14,,,,,D18:F-ThBr,,1883\r\n\"Z. Zheng, J. Wang, P. Bi, J. Ren, Y. Wang, Y. Yang, X. Liu, S. Zhang, J. Hou, Joule 2022, 6, 171.\",20.3,,,,,,,,,,,,,PBDB-TF:GS-ISO,,,,,,,1.8,1.38,,76.8,13.1,,,,,PBDM-TF:BTp-eC9,,2010\r\n\"Z. Zheng, J. Wang, P. Bi, J. Ren, Y. Wang, Y. Yang, X. Liu, S. Zhang, J. Hou, Joule 2022, 6, 171.\",20.3,,,,,,,,,,,,,PBDB-TF:GS-ISO,,,,,,,1.8,1.38,,76.8,13.1,,,,,PBDM-TF:BTp-eC9,,2010\r\n\"S. H. Kang, M. J. Jeong, Y. K. Eom, I. T. Choi, S. M. Kwon, Y. Yoo, J. Kim, J. Kwon, J. H. Park, H. K. Kim, Adv. Energy Mater. 2017, 7, 1602117.\",12.3,,,,,,,,,,,,,SGT-121/HC-A1,,,,,,,1.98,1.67,,65,10.3,,,,,SGT-021/HC-A4,,1825\r\n\"R. M. France, J. F. Geisz, T. Song, W. Olavarria, M. Young, A. Kibbler, M. A. Steiner, Joule 2022, 6, 1121.\",39.5,,,,,,,,,,,,,InGaAs,,,,,,,,0.92,\"1.33, 1.88\",85.3,15.4,,,\"GaAs, InGaP\",,,,3000\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\",37.7,,,,,,,,,,,,,InGaAs,,,,,,,,0.98,\"1.41, 1.89\",86,14.6,,,\"GaAs, InGaP\",,,,3014\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 657.\",35.9,,,,,,,,,,,,,Si,,,,,,,,1.13,\"1.48, 1.93\",84.3,13.1,,,\"GaInAsP, InGaP\",,,,3248\r\n\"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 657.\",28.1,,,,,,,,,,,,,CIGS,,,,,,,,1.01,\"1.50, 1.92\",81.1,11.7,,,AlGaAs/GaInP,,,,2952\r\n\"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2017, 25, 3.\",14,,,,,,,,,,,,,nc-Si,,,,,,,,1.3,\"1.27, 2.03\",73.4,9.9,,,\"nc-Si, a-Si\",,,,1922\r\n\"Y. Wang, T. Li, X. Chen, L. Zhang, Mater. Lett. 2022, 321, 132460.\",5.2,,,,,,,,,,FA0.8MA0.2SnBr0.2I2.8,,,,,,,,,1.41,,,,63.7,17.8,,,,,,,462\r\n\"M. Chen, Q. Dong, C. Xiao, X. Zheng, Z. Dai, Y. Shi, J. M. Luther, N. P. Padture, ACS Energy Lett. 2022, 7, 2256.\",8.5,,,,,,,,,,FAGe0.1Sn0.9I3,,,,,,,,,1.44,,,,62.9,20.8,,,,,,,650\r\n\"M. Chen, Q. Dong, C. Xiao, X. Zheng, Z. Dai, Y. Shi, J. M. Luther, N. P. Padture, ACS Energy Lett. 2022, 7, 2256.\",20.5,,,,,,,,,,FAMAPbI3,,,,,,,,,1.53,,,,81.2,23.6,,,,,,,1070\r\n\"Z. Zheng, F. Li, J. Gong, Y. Ma, J. Gu, X. Liu, S. Chen, M. Liu, Adv. Mater. 2022, 34, 2109879.\",22.4,,,,,,,,,,FAMAPbI3,,,,,,,,,1.54,,,,82.9,23.4,,,,,,,1151\r\n\"L. Yang, J. Feng, Z. Liu, Y. Duan, S. Zhan, S. Yang, K. He, Y. Li, Y. Zhou, N. Yuan, J. Ding, S. Liu, Adv. Mater. 2022, 34, 2201681.\",22.4,,,,,,,,,,Cs0.1FA0.9PbI3,,,,,,,,,1.54,,,,77.8,24.6,,,,,,,1170\r\n\"S. Wu, Z. Li, J. Zhang, X. Wu, X. Deng, Y. Liu, J. Zhou, C. Zhi, X. Yu, W. C. H. Choy, Z. Zhu, A. K. Y. Jen, Adv. Mater. 2021, 33, 2105539.\",21.7,,,,,,,,,,Cs0.05FA0.931MA0.019PbBr0.06I2.94/PM6:CH1007:PCBM,,,,,,,,,1.56,,,,77.7,24.8,,,,,,,1127\r\n\"X. Meng, X. Hu, Y. Zhang, Z. Huang, Z. Xing, C. Gong, L. Rao, H. Wang, F. Wang, T. Hu, L. Tan, Y. Song, Y. Chen, Adv. Funct. Mater. 2021, 31, 2106460.\",20.2,,,,,,,,,,FAMAPbBrI,,,,,,,,,1.59,,,,81.1,22.2,,,,,,,1120\r\n\"B. Fan, J. Xiong, Y. Zhang, C. Gong, F. Li, X. Meng, X. Hu, Z. Yuan, F. Wang, Y. Chen, Adv. Mater. 2022, 34, 2201840.\",20.6,,,,,,,,,,CsFAMAPbBrI,,,,,,,,,1.6,,,,80.7,23,,,,,,,1110\r\n\"Q. Dong, M. Chen, Y. Liu, F. T. Eickemeyer, W. Zhao, Z. Dai, Y. Yin, C. Jiang, J. Feng, S. Jin, S. Liu, S. M. Zakeeruddin, M. Grätzel, N. P. Padture, Y. Shi, Joule 2021, 5, 1587.\",20.5,,,,,,,,,,Cs0.04FA0.86MA0.1PbBr0.29I2.71,,,,,,,,,1.6,,,,76.5,23.5,,,,,,,1140\r\n\"B. Fan, J. Xiong, Y. Zhang, C. Gong, F. Li, X. Meng, X. Hu, Z. Yuan, F. Wang, Y. Chen, Adv. Mater. 2022, 34, 2201840.\",17.8,,,,,,,,,,CsFAMAPbBrI,,,,,,,,,1.6,,,,77.3,21.8,,,,,,,1060\r\n\"P. Sun, G. Qu, Q. Hu, Y. Ma, H. Liu, Z.-X. Xu, Z. Huang, ACS Appl. Energy Mater. 2022, 5, 3568.\",14.9,,,,,,,,,,MAPbI3,,,,,,,,,1.63,,,,67.3,21.5,,,,,,,1030\r\n\"Y. Han, Z. Hu, W. Zha, X. Chen, L. Yin, J. Guo, Z. Li, Q. Luo, W. Su, C.-Q. Ma, Adv. Mater. 2022, 34, 2110276.\",16.6,,,,,,,PM6:BTP-4Cl-12,,,,,,,,,,,,1.36,,,,75.4,26.8,,,,,,,821\r\n\"Y. Han, Z. Hu, W. Zha, X. Chen, L. Yin, J. Guo, Z. Li, Q. Luo, W. Su, C.-Q. Ma, Adv. Mater. 2022, 34, 2110276.\",12,,,,,,,PM6:BTP-4Cl-12,,,,,,,,,,,,1.38,,,,67.4,21.6,,,,,,,827\r\n\"G. Zeng, W. Chen, X. Chen, Y. Hu, Y. Chen, B. Zhang, H. Chen, W. Sun, Y. Shen, Y. Li, F. Yan, Y. Li, J. Am. Chem. Soc. 2022, 144, 8658.\",17.5,,,,,,,PM6:BTP-eC9:PC71BM,,,,,,,,,,,,1.38,,,,76.7,27.4,,,,,,,835\r\n\"Z. Chen, W. Song, K. Yu, J. Ge, J. Zhang, L. Xie, R. Peng, Z. Ge, Joule 2021, 5, 2395.\",15.9,,,,,,,D-18-Cl:G19:Y6,,,,,,,,,,,,1.39,,,,73.5,25,,,,,,,864\r\n\"Y. Chen, J. Wan, G. Xu, X. Wu, X. Li, Y. Shen, F. Yang, X. Ou, Y. Li, Y. Li, Sci China Chem 2022, 65, 1164.\",17.1,,,,,,,PBDB-T-2F:BTP-eC9:PC71BM,,,,,,,,,,,,1.4,,,,74.9,27.4,,,,,,,830\r\n\"N. Cui, Y. Song, C.-H. Tan, K. Zhang, X. Yang, S. Dong, B. Xie, F. Huang, npj Flexible Electron. 2021, 5, 31.\",15.2,,,,,,,PM6:Y6,,,,,,,,,,,,1.41,,,,73.3,25,,,,,,,830\r\n\"B. Murali, K. Gireesh Baiju, R. Krishna Prasad, K. Jayanarayanan, D. Kumaresan, Sustainable Energy Fuels 2022, 6, 2503.\",3.9,,,,,,,,,,,,,,,,,,,2.02,,,,45.2,11.9,,,,N719,,,720\r\n\"J. Schön, G. M. M. W. Bissels, P. Mulder, R. H. van Leest, N. Gruginskie, E. Vlieg, D. Chojniak, D. Lackner, Prog. Photovoltaics 2022, 30, 1003.\",30.2,,,,,,,,,,,,,,Ga0.73In0.27As,,,,,,\"1.41, 1.91 \",1,,84.5,16.1,,,,,,\"GaAs, Ga0.51In0.49P \",3043\r\n\"L. Li, Y. Wang, X. Wang, R. Lin, X. Luo, Z. Liu, K. Zhou, S. Xiong, Q. Bao, G. Chen, Y. Tian, Y. Deng, K. Xiao, J. Wu, M. I. Saidaminov, H. Lin, C.-Q. Ma, Z. Zhao, Y. Wu, L. Zhang, H. Tan, Nat. Energy 2022, 7, 708.\",24.7,,,,,,,,,,,,,,FA0.7MA0.3Pb0.5Sn0.5I3,,,,,,1.78,1.25,,78.3,15.8,,,,,,FA0.8Cs0.2PbI1.95Br1.05,2000\r\n\"L. Li, Y. Wang, X. Wang, R. Lin, X. Luo, Z. Liu, K. Zhou, S. Xiong, Q. Bao, G. Chen, Y. Tian, Y. Deng, K. Xiao, J. Wu, M. I. Saidaminov, H. Lin, C.-Q. Ma, Z. Zhao, Y. Wu, L. Zhang, H. Tan, Nat. Energy 2022, 7, 708.\",24.4,,,,,,,,,,,,,,FA0.7MA0.3Pb0.5Sn0.5I3,,,,,,1.78,1.25,,77.3,15.6,,,,,,FA0.8Cs0.2PbI1.95Br1.05,2016\r\n\"H. Lai, J. Luo, Y. Zwirner, S. Olthof, A. Wieczorek, F. Ye, Q. Jeangros, X. Yin, F. Akhundova, T. Ma, R. He, R. K. Kothandaraman, X. Chin, E. Gilshtein, A. Müller, C. Wang, J. Thiesbrummel, S. Siol, J. M. Prieto, T. Unold, M. Stolterfoht, C. Chen, A. N. Tiwari, D. Zhao, F. Fu, Adv. Energy Mater. 2022, 12, 2202438.\",23.8,,,,,,,,,,,,,,FA0.6MA0.4Pb0.4Sn0.6I3,,,,,,1.79,1.26,,75.1,15.1,,,,,,Cs0.12FA0.8MA0.08PbI1.8Br1.2,2.1\r\n\"L. Sun, W. Wang, L. Hao, Z. Jia, Y. Zhao, G. Zhi, H. Yao, Mater. Sci. Semicond. Process. 2022, 138, 106301.\",4.4,,,,,,,,\"Cu2CdxZn1 xSn(S,Se)4\",,,,,,,,,,,1.04,,,,46.4,23.9,,,,,,,394\r\n\"L. Sun, W. Wang, L. Hao, A. Raza, Y. Zhao, Z. Tang, G. Zhi, H. Yao, Ceram. Int. 2022, 48, 19891.\",4.9,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,,1.07,,,,47.3,28.7,,,,,,,358\r\n\"W. Xie, Q. Sun, Q. Yan, J. Wu, C. Zhang, Q. Zheng, Y. Lai, H. Deng, S. Cheng, Small 2022, 18, 2201347.\",10.2,,,,,,,,\"Cu2ZnSn(S,Se)4\",,,,,,,,,,,1.13,,,,62,35.7,,,,,,,463\r\n\"Q. Zhao, H. Shen, Y. Xu, K. Gao, D. Chen, Y. Li, ACS Appl. Energy Mater. 2022, 5, 3668.\",6.5,,,,,,,,CZTSSe,,,,,,,,,,,1.59,,,,48,22.6,,,,,,,601\r\n\"D.-Y. Jung, Y.-R. Jeong, M. S. Mina, S.-E. Lee, E. Enkhbayar, J. Kim, Curr. Appl. Phys. 2022, 41, 66.\",11.5,,,,,,,,,CIGSSe,,,,,,,,,,1.11,,,,64.6,33.8,,,,,,,526\r\n\"S. Pouladi, C. Favela, W. Wang, M. Moradnia, N.-I. Kim, S. Shervin, J. Chen, S. Sharma, G. Yang, M.-C. Nguyen, R. Choi, J. Kim, A. Fedorenko, B. Bogner, J. Bao, S. M. Hubbard, V. Selvamanickam, J.-H. Ryou, Sol. Energy Mater. Sol. Cells 2022, 243, 111791.\",13.5,,,,,,,,,GaAs,,,,,,,,,,1.45,,,,77.7,22.1,,,,,,,786\r\n\"W. L. Rance, J. M. Burst, D. M. Meysing, C. A. Wolden, M. O. Reese, T. A. Gessert, W. K. Metzger, S. Garner, P. Cimo, T. M. Barnes, Appl. Phys. Lett. 2014, 104, 143903.\",14.1,,,,,,,,,CdTe,,,,,,,,,,1.46,,,,70.3,24.334,,,,,,,821\r\n\"B. Tyagi, H. B. Lee, N. Kumar, W.-Y. Jin, K.-J. Ko, M. M. Ovhal, R. Sahani, H.-J. Chung, J. Seo, J.-W. Kang, Nano Energy 2022, 95, 106978.\",16.3,,,,,3,Cs0.25FA0.75PbBr0.6I2.4,,,,,,,,,,,,,1.67,,,,78.3,18.9,,,,,,,1099\r\n\"S. Seo, K. Akino, J.-S. Nam, A. Shawky, H.-S. Lin, H. Nagaya, E. I. Kauppinen, R. Xiang, Y. Matsuo, I. Jeon, S. Maruyama, Adv. Mater. Interfaces 2022, 9, 2101595.\",19.1,,,,,5,MAPbI3,,,,,,,,,,,,,1.6,,,,73.4,23.2,,,,,,,1120\r\n\"S. Yoon, H. U. Ha, H.-J. Seok, H.-K. Kim, D.-W. Kang, Adv. Funct. Mater. 2022, 32, 2111760.\",17.8,,,,,9,Cs0.13FA0.87PbBr0.39I2.61,,,,,,,,,,,,,1.63,,,,82.7,19.3,,,,,,,1120\r\n\"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\",13.2,,,,,13,Cs0.25FA0.75PbBr1.5I1.5,,,,,,,,,,,,,1.88,,,,74.1,13.8,,,,,,,1298\r\n\"S. Lie, A. Bruno, L. H. Wong, L. Etgar, ACS Appl. Mater. Interfaces 2022, 14, 11339.\",11.4,,,,,15,Cs0.05FA0.775MA0.1615PbBr0.51I2.49,,,,,,,,,,,,,1.64,,,,62,16.8,,,,,,,1094\r\n\"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\",8.6,,,,,23,Cs0.25FA0.75PbBr1.5I1.5,,,,,,,,,,,,,1.88,,,,69.9,10,,,,,,,1236\r\n\"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\",12,,,,,35,Cs0.25FA0.75PbBr1.5I1.5,,,,,,,,,,,,,1.88,,,,72.3,12.9,,,,,,,1289\r\n\"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\",4.1,,,,,52,Cs0.25FA0.75PbBr1.5I1.5,,,,,,,,,,,,,1.88,,,,63,5.8,,,,,,,1125\r\n\"D. Han, S. Han, Z. Bu, Y. Deng, C. Liu, W. Guo, Sol. RRL 2022, 6, 2200441.\",12.7,,,,,8,,,,,,D18-Cl:Y6:PC71BM,,,,,,,,1.41,,,,70.4,21.1,,,,,,,852\r\n\"L. Zheng, M. Li, S. Dai, Y. Wu, Y. Cai, X. Zhu, S. Ma, D. Yun, J.-F. Li, J. Phys. Chem. C 2021, 125, 18623.\",13.6,,,,,19,,,,,,PM6:Y7,,,,,,,,1.42,,,,70.2,23.4,,,,,,,830\r\n\"W. Liu, S. Sun, L. Zhou, Y. Cui, W. Zhang, J. Hou, F. Liu, S. Xu, X. Zhu, Angew. Chem., Int. Ed. 2022, 61, 202116111.\",14,,,,,20,,,,,,PM6:Y6:SN3,,,,,,,,1.37,,,,74.3,23,,,,,,,820\r\n\"S. Liu, H. Li, X. Wu, D. Chen, L. Zhang, X. Meng, L. Tan, X. Hu, Y. Chen, Adv. Mater. 2022, 34, 2201604.\",14.6,,,,,20,,,,,,PM6/ICBA:Y6,,,,,,,,1.39,,,,74.7,22.8,,,,,,,860\r\n\"W. Liu, S. Sun, S. Xu, H. Zhang, Y. Zheng, Z. Wei, X. Zhu, Adv. Mater. 2022, 34, 2200337.\",11.6,,,,,20,,,,,,BTB7-Th:ATT-9,,,,,,,,1.23,,,,68.2,25.6,,,,,,,661\r\n\"X. Yuan, R. Sun, Y. Wu, T. Wang, Y. Wang, W. Wang, Y. Yu, J. Guo, Q. Wu, J. Min, Adv. Funct. Mater. 2022, 32, 2200107.\",16.1,,,,,21,,,,,,PM6-Ir1:BTP-eC9:PC71BM,,,,,,,,1.39,,,,76.1,24.6,,,,,,,859\r\n\"H. I. Jeong, S. Biswas, S. C. Yoon, S.-J. Ko, H. Kim, H. Choi, Adv. Energy Mater. 2021, 11, 2102397.\",12.1,,,,,25,,,,,,PM6:Y6,,,,,,,,1.43,,,,66.6,23.9,,,,,,,760\r\n\"J. Jing, S. Dong, K. Zhang, Z. Zhou, Q. Xue, Y. Song, Z. Du, M. Ren, F. Huang, Adv. Energy Mater. 2022, 12, 2200453.\",11.3,,,,,28,,,,,,PM6:Y6-BO,,,,,,,,1.39,,,,70.3,19.7,,,,,,,816\r\n\"X. Huang, L. Zhang, Y. Cheng, J. Oh, C. Li, B. Huang, L. Zhao, J. Deng, Y. Zhang, Z. Liu, F. Wu, X. Hu, C. Yang, L. Chen, Y. Chen, Adv. Funct. Mater. 2022, 32, 2108634.\",12,,,,,31,,,,,,PCE10-BDT2F-0.8:Y6,,,,,,,,1.39,,,,69.5,22.8,,,,,,,758\r\n\"D. Wang, Y. Li, G. Zhou, E. Gu, R. Xia, B. Yan, J. Yao, H. Zhu, X. Lu, H.-L. Yip, H. Chen, C.-Z. Li, Energy Environ. Sci. 2022, 15, 2629.\",11.2,,,,,32,,,,,,PM6:m-BTP-PhC6:BO-Cl,,,,,,,,1.42,,,,77.6,17,,,,,,,849\r\n\"S. Guan, Y. Li, K. Yan, W. Fu, L. Zuo, H. Chen, Adv. Mater. 2022, 34, 2205844.\",13,,,,,39,,,,,,PBDB-TF:L8-BO:BTP-eC9,,,,,,,,1.41,,,,80.3,19,,,,,,,849\r\n\"H. I. Jeong, S. Biswas, S. C. Yoon, S.-J. Ko, H. Kim, H. Choi, Adv. Energy Mater. 2021, 11, 2102397.\",9.7,,,,,25,,,,,,PM6:Y6,,,,,,,,1.43,,,,63,20,,,,,,,770\r\n\"X. Liu, Z. Zhong, R. Zhu, J. Yu, G. Li, Joule 2022, 6, 1918.\",11.4,,,,,47,,,,,,PM6:BTP-eC9:L8-BO,,,,,,,,1.39,,,,74.5,18,,,,,,,854\r\n\"X. Xie, Y. Zhang, Y. Ren, L. He, Y. Yuan, J. Zhang, P. Wang, J. Phys. Chem. C 2022, 126, 11007.\",11,,,,,5,,,,,,,,,,,,,,1.8,,,,75.2,16.8,,,,C268 + Y1,,,871\r\n\"A. K. Bharwal, L. Manceriu, C. Olivier, A. Mahmoud, C. Iojoiu, T. Toupance, C. M. Ruiz, M. Pasquinelli, D. Duché, J.-J. Simon, C. Henrist, F. Alloin, Chem. Eng. J. 2022, 446, 136777.\",5,,,,,10,,,,,,,,,,,,,,1.81,,,,60.7,11.7,,,,N719,,,710\r\n\"F. Odobel, T. Baron, W. Naim, I. Nikolinakos, B. Andrin, Y. Pellegrin, D. Jacquemin, S. Haacke, F. Sauvage, Angew. Chem., Int. Ed. 2022, 61, 202207459.\",2.5,,,,,75,,,,,,,,,,,,,,1.53,,,,56.2,10.9,,,,TB207,,,408\r\n\"C. Yang, M. Moemeni, M. Bates, W. Sheng, B. Borhan, R. R. Lunt, Adv. Opt. Mater. 2020, 8, 1901536.\",1.2,,,,,74,,,,,,,,,,,,,,1.5,,,,81.3,1.5,COi8DFIC/GaAs,,,,,,990\r\n\"C. Yang, W. Sheng, M. Moemeni, M. Bates, C. K. Herrera, B. Borhan, R. R. Lunt, Adv. Energy Mater. 2021, 11, 2003581.\",3,,,,,75,,,,,,,,,,,,,,1.64,,,,77.7,3.8,Cs2Mo6I8(CF3CF2COO)6:BODIPY/GaAs,,,,,,1020\r\n\"Y. Zhao, R. R. Lunt, Adv. Energy Mater. 2013, 3, 1143.\",0.4,,,,,84,,,,,,,,,,,,,,1.11,,,,65.1,1.3,(TBA)2Mo6Cl14/Si,,,,,,520\r\n\"Y. Zhao, G. A. Meek, B. G. Levine, R. R. Lunt, Adv. Opt. Mater. 2014, 2, 606.\",0.4,,,,,86,,,,,,,,,,,,,,1.52,,,,66.7,1.2,Cy7-NHS/Si,,,,,,500\r\n\"['J. Sanchez-Diaz, R. S. Sánchez, S. Masi, M. Kreĉmarová, A. O. Alvarez, E. M. Barea, J. Rodriguez-Romero, V. S. Chirvony, J. F. Sánchez-Royo, J. P. Martinez-Pastor, I. Mora-Seró, Joule 2022, 6, 861.', 'J. Sanchez-Diaz, R. S. Sánchez, S. Masi, M. Kreĉmarová, A. O. Alvarez, E. M. Barea, J. Rodriguez-Romero, V. S. Chirvony, J. F. Sánchez-Royo, J. P. Martinez-Pastor, I. Mora-Seró, https://emerging-pv.org/wp-content/uploads/2022/06/Add_SI_Stability-PSC_Joule.2022.02.014.pdf (accessed: June 2022).']\",,9.4,9.4,,9.2,,FASnI3+NaBH4+DipI,,,,,,,,,\"MPP, AM1.5G, N2, 70 °C\",,1.9,9.3,1.4,,,,,,,,,,,,\r\n\"T. Wu, X. Liu, X. Luo, H. Segawa, G. Tong, Y. Zhang, L. K. Ono, Y. Qi, L. Han, Nano-Micro Lett. 2022, 14, 99.\",,13.8,14.1,,13,,FASnI3,,,,,,,,,\"MPP, AM1.5G, air\",,2.8,13.6,1.45,,,,,,,,,,,,\r\n\"F. Zhang, Y. Park So, C. Yao, H. Lu, P. Dunfield Sean, C. Xiao, S. Uličná, X. Zhao, L. Du Hill, X. Chen, X. Wang, E. Mundt Laura, H. Stone Kevin, T. Schelhas Laura, G. Teeter, S. Parkin, L. Ratcliff Erin, Y.-L. Loo, J. Berry Joseph, C. Beard Matthew, Y. Yan, W. Larson Bryon, K. Zhu, Science 2022, 375, 71.\",,23.1,22.7,,20.7,,FA0.97MA0.03PbI2.91Br0.09,,,,,,,,,\"MPP, AM1.5G, N2, 40 °C\",,4.6,22,1.53,,,,,,,,,,,,\r\n\"X. Li, W. Zhang, X. Guo, C. Lu, J. Wei, J. Fang, Science 2022, 375, 434.\",,19.8,20.6,,17.7,,FA0.95MA0.05PbBr0.15I2.85,,,,,,,,,\"MPP, w-LED, air, 55 °C\",,4.1,19.1,1.57,,,,,,,,,,,,\r\n\"J. Peng, F. Kremer, D. Walter, Y. Wu, Y. Ji, J. Xiang, W. Liu, T. Duong, H. Shen, T. Lu, F. Brink, D. Zhong, L. Li, O. Lee Cheong Lem, Y. Liu, K. J. Weber, T. P. White, K. R. Catchpole, Nature 2022, 601, 573.\",,23.1,22.9,, ,,Cs0.05FA0.9MA0.05 Pb Br0.26I2.74,,,,,,,,,\"MPP, N2\",,4.6, ,1.58,,,,,,,,,,,,\r\n\"Q. Zhou, C. Cai, Q. Xiong, Z. Zhang, J. Xu, L. Liang, S. Wang, W. Sun, Z. Yuan, P. Gao, Adv. Energy Mater. 2022, 12, 2201243.\",,23.6,20.2,, ,,FA0.92MA0.08PbBr0.24I2.76,,,,,,,,,\"MPP, AM1.5G, air, 50% RH\",,4.4, ,1.58,,,,,,,,,,,,\r\n\"B. Fan, J. Xiong, Y. Zhang, C. Gong, F. Li, X. Meng, X. Hu, Z. Yuan, F. Wang, Y. Chen, Adv. Mater. 2022, 34, 2201840.\",,19.6,18.4,,16.3,,CsFAMAPbBrI,,,,,,,,,\"MPP, AM1.5G, air, 40% RH, 30 °C\",,3.8,17.4,1.6,,,,,,,,,,,,\r\n\"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\",,25.6,26.4,,17.8,,,,,,,,1.25,,FA0.8Cs0.2Pb(I0.62Br0.38)3,\"MPP, AM1.5G, air 30–50% RH, 35 °C\",,5.2,23.5,,1.8,,,,,,,,,,FA0.7MA0.3Pb0.5Sn0.5I3,\r\n"
  },
  {
    "path": "dataset/Emerging PV database/new_merged_ver123.json",
    "content": "[{\"Refs.\": \"T. Jiang, Z. Chen, X. Chen, T. Liu, X. Chen, W. E. I. Sha, H. Zhu, Y. Yang, Sol. RRL 2020, 4, 1900467.\", \"PCE [%]\": \"20.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FASnI3)0.6(MAPbI3)0.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.25\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"30.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"843.0\"}, {\"Refs.\": \"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"GuaSCN:(FASnI3)0.6(MAPbI3)0.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.26\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"30.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"834.0\"}, {\"Refs.\": \"C. Li, Z. Song, D. Zhao, C. Xiao, B. Subedi, N. Shrestha, M. M. Junda, C. Wang, C.-S. Jiang, M. Al-Jassim, R. J. Ellingson, N. J. Podraza, K. Zhu, Y. Yan, Adv. Energy Mater. 2019, 9, 1803135.\", \"PCE [%]\": \"19.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FASnI3)0.6(MAPbI3)0.34(MAPbBr3)0.06\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.26\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.5\", \"Jsc [mA cm\\u22122]\": \"28.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"888.0\"}, {\"Refs.\": \"R. Lin, K. Xiao, Z. Qin, Q. Han, C. Zhang, M. Wei, M. I. Saidaminov, Y. Gao, J. Xu, M. Xiao, A. Li, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2019, 4, 864.\", \"PCE [%]\": \"20.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA0.3FA0.7Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.27\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.5\", \"Jsc [mA cm\\u22122]\": \"31.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"827.0\"}, {\"Refs.\": \"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.5MA0.45Cs0.05Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"30.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"G. Kapil, T. Bessho, C. H. Ng, K. Hamada, M. Pandey, M. A. Kamarudin, D. Hirotani, T. Kinoshita, T. Minemoto, Q. Shen, T. Toyoda, T. N. Murakami, H. Segawa, S. Hayase, ACS Energy Lett. 2019, 4, 1991.\", \"PCE [%]\": \"18.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.025FA0.475MA0.5Sn0.5Pb0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"32.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"S. Shao, Y. Cui, H. Duim, X. Qiu, J. Dong, G. H. ten Brink, G. Portale, R. C. Chiechi, S. Zhang, J. Hou, M. A. Loi, Adv. Mater. 2018, 30, 1803703.\", \"PCE [%]\": \"16.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASn0.5Pb0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.29\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"29.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"771.0\"}, {\"Refs.\": \"T. S. Ripolles, D. Yamasuso, Y. Zhang, M. A. Kamarudin, C. Ding, D. Hirotani, Q. Shen, S. Hayase, J. Phys. Chem. C 2018, 122, 27284.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FASnI3)0.6(MAPbI3)0.3(MAPbBr3)0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.29\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"26.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"M. Liu, Z. Chen, Z. Chen, H.-L. Yip, Y. Cao, Mater. Chem. Front. 2019, 3, 496.\", \"PCE [%]\": \"13.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.5MA0.5Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.1\", \"Jsc [mA cm\\u22122]\": \"29.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"660.0\"}, {\"Refs.\": \"Y. Wang, J. Tu, T. Li, C. Tao, X. Deng, Z. Li, J. Mater. Chem. A 2019, 7, 7683.\", \"PCE [%]\": \"5.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsSnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"50.3\", \"Jsc [mA cm\\u22122]\": \"23.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"420.0\"}, {\"Refs.\": \"F. Li, C. Zhang, J.-H. Huang, H. Fan, H. Wang, P. Wang, C. Zhan, C.-M. Liu, X. Li, L.-M. Yang, Y. Song, K.-J. Jiang, Angew. Chem., Int. Ed. 2019, 58, 6688.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.0\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"486.0\"}, {\"Refs.\": \"G. E. Eperon, T. Leijtens, K. A. Bush, R. Prasanna, T. Green, J. T.-W. Wang, D. P. McMeekin, G. Volonakis, R. L. Milot, R. May, A. Palmstrom, D. J. Slotcavage, R. A. Belisle, J. B. Patel, E. S. Parrott, R. J. Sutton, W. Ma, F. Moghadam, B. Conings, A. Babayigit, H.-G. Boyen, S. Bent, F. Giustino, L. M. Herz, M. B. Johnston, M. D. McGehee, H. J. Snaith, Science 2016, 354, 861.\", \"PCE [%]\": \"14.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.75Cs0.25Sn0.5Pb0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.4\", \"Jsc [mA cm\\u22122]\": \"26.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"740.0\"}, {\"Refs.\": \"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.4Sn0.6I2.8Br0.2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.9\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. G\\u00f6del, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.4Sn0.6I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.6\", \"Jsc [mA cm\\u22122]\": \"20.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"767.0\"}, {\"Refs.\": \"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.4Sn0.6I2.6Br0.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.1\", \"Jsc [mA cm\\u22122]\": \"20.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"X. Lian, J. Chen, Y. Zhang, M. Qin, J. Li, S. Tian, W. Yang, X. Lu, G. Wu, H. Chen, Adv. Funct. Mater. 2019, 29, 1807024.\", \"PCE [%]\": \"16.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPb0.7Sn0.3I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"26.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"M. Zhang, D. Chi, J. Wang, F. Wu, S. Huang, Sol. Energy 2020, 201, 589.\", \"PCE [%]\": \"14.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.3MA0.7Pb0.7Sn0.3I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.6\", \"Jsc [mA cm\\u22122]\": \"27.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"737.0\"}, {\"Refs.\": \"D. Chi, S. Huang, M. Zhang, S. Mu, Y. Zhao, Y. Chen, J. You, Adv. Funct. Mater. 2018, 28, 1804603.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPb0.75Sn0.25I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.4\", \"Jsc [mA cm\\u22122]\": \"28.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"H. L. Zhu, J. Xiao, J. Mao, H. Zhang, Y. Zhao, W. C. H. Choy, Adv. Funct. Mater. 2017, 27, 1605469.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.75Sn0.25I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.5\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"800.0\"}, {\"Refs.\": \"X. Zhou, L. Zhang, X. Wang, C. Liu, S. Chen, M. Zhang, X. Li, W. Yi, B. Xu, Adv. Mater. 2020, 32, 1908107.\", \"PCE [%]\": \"20.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.7MA0.3Pb0.7Sn0.3I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.0\", \"Jsc [mA cm\\u22122]\": \"26.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. G\\u00f6del, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.6Sn0.4I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.8\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"745.0\"}, {\"Refs.\": \"P. Wang, F. Li, K.-J. Jiang, Y. Zhang, H. Fan, Y. Zhang, Y. Miao, J.-H. Huang, C. Gao, X. Zhou, F. Wang, L.-M. Yang, C. Zhan, Y. Song, Adv. Sci. 2020, 7, 1903047.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.2\", \"Jsc [mA cm\\u22122]\": \"20.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"570.0\"}, {\"Refs.\": \"D. B. Khadka, Y. Shirai, M. Yanagida, K. Miyano, J. Mater. Chem. C 2020, 8, 2307.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA1\\u2212xRbxSnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.6\", \"Jsc [mA cm\\u22122]\": \"20.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"487.0\"}, {\"Refs.\": \"Z. Yang, A. Rajagopal, C.-C. Chueh, S. B. Jo, B. Liu, T. Zhao, A. K. Y. Jen, Adv. Mater. 2016, 28, 8990.\", \"PCE [%]\": \"14.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.75Sn0.25I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"22.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"M. M. Tavakoli, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Z. Fan, Adv. Mater. 2018, 30, 1705998.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.7Sn0.3I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.4\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"772.0\"}, {\"Refs.\": \"T. Wu, X. Liu, X. He, Y. Wang, X. Meng, T. Noda, X. Yang, L. Han, Sci. China Chem. 2020, 63, 107.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"21.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"T. Wu, X. Liu, X. He, Y. Wang, X. Meng, T. Noda, X. Yang, L. Han, Sci. China Chem. 2020, 63, 107.\", \"PCE [%]\": \"9.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.4\", \"Jsc [mA cm\\u22122]\": \"21.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"606.0\"}, {\"Refs.\": \"K. Nishimura, M. A. Kamarudin, D. Hirotani, K. Hamada, Q. Shen, S. Iikubo, T. Minemoto, K. Yoshino, S. Hayase, Nano Energy 2020, 74, 104858.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.9EA0.1)0.98EDA0.01SnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"Y. Zhao, X. Xu, H. Zhang, J. Shi, L. Zhu, H. Wu, D. Li, Y. Luo, Q. Meng, J. Power Sources 2017, 359, 147.\", \"PCE [%]\": \"19.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.6MA0.4PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.51\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"23.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1047.0\"}, {\"Refs.\": \"S. Yuan, Y. Cai, S. Yang, H. Zhao, F. Qian, Y. Han, J. Sun, Z. Liu, S. Liu, Sol. RRL 2019, 3, 1900220.\", \"PCE [%]\": \"22.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.85MA0.15PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.6\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"H. Min, M. Kim, S.-U. Lee, H. Kim, G. Kim, K. Choi, J. H. Lee, S. I. Seok, Science 2019, 366, 749.\", \"PCE [%]\": \"23.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\\u03b1-FAPbI3:MDACl2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"26.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1144.0\"}, {\"Refs.\": \"Q. Jiang, Y. Zhao, X. Zhang, X. Yang, Y. Chen, Z. Chu, Q. Ye, X. Li, Z. Yin, J. You, Nat. Photonics 2019, 13, 460.\", \"PCE [%]\": \"23.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA1\\u2212xMAxPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.4\", \"Jsc [mA cm\\u22122]\": \"25.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1180.0\"}, {\"Refs.\": \"T. Niu, J. Lu, M.-C. Tang, D. Barrit, D.-M. Smilgies, Z. Yang, J. Li, Y. Fan, T. Luo, I. McCulloch, A. Amassian, S. Liu, K. Zhao, Energy Environ. Sci. 2018, 11, 3358.\", \"PCE [%]\": \"18.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1050.0\"}, {\"Refs.\": \"D. Yang, R. Yang, K. Wang, C. Wu, X. Zhu, J. Feng, X. Ren, G. Fang, S. Priya, S. Liu, Nat. Commun. 2018, 9, 3239.\", \"PCE [%]\": \"21.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.95Cs0.05PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"24.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"M. Jeong, I. W. Choi, E. M. Go, Y. Cho, M. Kim, B. Lee, S. Jeong, Y. Jo, H. W. Choi, J. Lee, J.-H. Bae, S. K. Kwak, D. S. Kim, C. Yang, Science 2020, 369, 1615.\", \"PCE [%]\": \"24.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.6\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1181.0\"}, {\"Refs.\": \"W. S. Yang, B.-W. Park, E. H. Jung, N. J. Jeon, Y. C. Kim, D. U. Lee, S. S. Shin, J. Seo, E. K. Kim, J. H. Noh, S. I. Seok, Science 2017, 356, 1376.\", \"PCE [%]\": \"22.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.9(MAPbBr3)0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.3\", \"Jsc [mA cm\\u22122]\": \"25.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1105.0\"}, {\"Refs.\": \"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\", \"PCE [%]\": \"21.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.70MA0.25PbI3-DAP\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1160.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\", \"PCE [%]\": \"25.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \" \", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.8\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1180.0\"}, {\"Refs.\": \"E. H. Jung, N. J. Jeon, E. Y. Park, C. S. Moon, T. J. Shin, T.-Y. Yang, J. H. Noh, J. Seo, Nature 2019, 567, 511.\", \"PCE [%]\": \"22.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.95(MAPbBr3)0.05\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.9\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1145.0\"}, {\"Refs.\": \"Q. Jiang, Z. Chu, P. Wang, X. Yang, H. Liu, Y. Wang, Z. Yin, J. Wu, X. Zhang, J. You, Adv. Mater. 2017, 29, 1703852.\", \"PCE [%]\": \"20.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)1\\u2212x(MAPbBr3)x\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"24.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1116.0\"}, {\"Refs.\": \"Z. Chen, X. Zheng, F. Yao, J. Ma, C. Tao, G. Fang, J. Mater. Chem. A 2018, 6, 17625.\", \"PCE [%]\": \"19.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(MA0.7FA0.3)0.97EDA0.015PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"23.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1075.0\"}, {\"Refs.\": \"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\", \"PCE [%]\": \"23.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.6\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\", \"PCE [%]\": \"22.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.0\", \"Jsc [mA cm\\u22122]\": \"23.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1143.0\"}, {\"Refs.\": \"L. Meng, C. Sun, R. Wang, W. Huang, Z. Zhao, P. Sun, T. Huang, J. Xue, J.-W. Lee, C. Zhu, Y. Huang, Y. Li, Y. Yang, J. Am. Chem. Soc. 2018, 140, 17255.\", \"PCE [%]\": \"20.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)1\\u2212x(MAPbBr3)x\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.5\", \"Jsc [mA cm\\u22122]\": \"22.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"J. J. Yoo, S. Wieghold, M. C. Sponseller, M. R. Chua, S. N. Bertram, N. T. P. Hartono, J. S. Tresback, E. C. Hansen, J.-P. Correa-Baena, V. Bulovi\\u0107, T. Buonassisi, S. S. Shin, M. G. Bawendi, Energy Environ. Sci. 2019, 12, 2192.\", \"PCE [%]\": \"22.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.92(MAPbBr3)0.08\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.6\", \"Jsc [mA cm\\u22122]\": \"24.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1186.0\"}, {\"Refs.\": \"H. B. Lee, N. Kumar, M. M. Ovhal, Y. J. Kim, Y. M. Song, J.-W. Kang, Adv. Funct. Mater. 2020, 30, 2001559.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(FAPbI3)0.85(MAPbBr3)0.15\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.8\", \"Jsc [mA cm\\u22122]\": \"23.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1125.0\"}, {\"Refs.\": \"P. Cui, D. Wei, J. Ji, H. Huang, E. Jia, S. Dou, T. Wang, W. Wang, M. Li, Nat. Energy 2019, 4, 150.\", \"PCE [%]\": \"21.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.15MA0.85PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.6\", \"Jsc [mA cm\\u22122]\": \"24.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"M. Li, Z.-K. Wang, M.-P. Zhuo, Y. Hu, K.-H. Hu, Q.-Q. Ye, S. M. Jain, Y.-G. Yang, X.-Y. Gao, L.-S. Liao, Adv. Mater. 2018, 30, 1800258.\", \"PCE [%]\": \"21.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.9Sn0.05Cu0.05I2.9Br0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.0\", \"Jsc [mA cm\\u22122]\": \"24.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1086.0\"}, {\"Refs.\": \"X. Zheng, B. Chen, J. Dai, Y. Fang, Y. Bai, Y. Lin, H. Wei, X. C. Zeng, J. Huang, Nat. Energy 2017, 2, 17102.\", \"PCE [%]\": \"21.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.85MA0.15Pb(I0.85Br0.15)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.7\", \"Jsc [mA cm\\u22122]\": \"23.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"L. Wang, H. Zhou, J. Hu, B. Huang, M. Sun, B. Dong, G. Zheng, Y. Huang, Y. Chen, L. Li, Z. Xu, N. Li, Z. Liu, Q. Chen, L.-D. Sun, C.-H. Yan, Science 2019, 363, 265.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\\u2212xClx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.4\", \"Jsc [mA cm\\u22122]\": \"23.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1130.0\"}, {\"Refs.\": \"P. Cui, D. Wei, J. Ji, H. Huang, E. Jia, S. Dou, T. Wang, W. Wang, M. Li, Nat. Energy 2019, 4, 150.\", \"PCE [%]\": \"20.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"25.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"X. Zhao, C. Yao, T. Liu, J. C. Hamill Jr., G. O. Ngongang Ndjawa, G. Cheng, N. Yao, H. Meng, Y.-L. Loo, Adv. Mater. 2019, 31, 1904494.\", \"PCE [%]\": \"21.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.1\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"M. A. Mahmud, T. Duong, Y. Yin, H. T. Pham, D. Walter, J. Peng, Y. Wu, L. Li, H. Shen, N. Wu, N. Mozaffari, G. Andersson, K. R. Catchpole, K. J. Weber, T. P. White, Adv. Funct. Mater. 2020, 30, 1907962.\", \"PCE [%]\": \"22.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.07Rb0.03FA0.765MA0.135PbI2.55Br0.45\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.5\", \"Jsc [mA cm\\u22122]\": \"24.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1200.0\"}, {\"Refs.\": \"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\", \"PCE [%]\": \"21.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3-DAP\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.7\", \"Jsc [mA cm\\u22122]\": \"22.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1180.0\"}, {\"Refs.\": \"K. Choi, J. Lee, H. I. Kim, C. W. Park, G.-W. Kim, H. Choi, S. Park, S. A. Park, T. Park, Energy Environ. Sci. 2018, 11, 3238.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.76MA0.19PbBr0.6I2.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.8\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1130.0\"}, {\"Refs.\": \"X. Zhao, C. Yao, T. Liu, J. C. Hamill Jr., G. O. Ngongang Ndjawa, G. Cheng, N. Yao, H. Meng, Y.-L. Loo, Adv. Mater. 2019, 31, 1904494.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.8\", \"Jsc [mA cm\\u22122]\": \"23.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"N. J. Jeon, J. H. Noh, Y. C. Kim, W. S. Yang, S. Ryu, S. I. Seok, Nat. Mater. 2014, 13, 897.\", \"PCE [%]\": \"16.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI1\\u2212xBrx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"19.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1109.0\"}, {\"Refs.\": \"J. H. Noh, S. H. Im, J. H. Heo, T. N. Mandal, S. I. Seok, Nano Lett. 2013, 13, 1764.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.87Br0.13)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.4\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"904.0\"}, {\"Refs.\": \"S. A. Kulkarni, T. Baikie, P. P. Boix, N. Yantara, N. Mathews, S. Mhaisalkar, J. Mater. Chem. A 2014, 2, 9221.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.88Br0.12)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.8\", \"Jsc [mA cm\\u22122]\": \"13.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"20.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05MA0.15FA0.8Pb(I0.75Br0.25)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.7\", \"Jsc [mA cm\\u22122]\": \"21.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1220.0\"}, {\"Refs.\": \"M. Chen, M.-G. Ju, H. F. Garces, A. D. Carl, L. K. Ono, Z. Hawash, Y. Zhang, T. Shen, Y. Qi, R. L. Grimm, D. Pacifici, X. C. Zeng, Y. Zhou, N. P. Padture, Nat. Commun. 2019, 10, 16.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.74Br0.26)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"10.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"936.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"16.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8Pb(I0.75Br0.25)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.5\", \"Jsc [mA cm\\u22122]\": \"20.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"M.-J. Wu, C.-C. Kuo, L.-S. Jhuang, P.-H. Chen, Y.-F. Lai, F.-C. Chen, Adv. Energy Mater. 2019, 9, 1901863.\", \"PCE [%]\": \"12.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA0.85Cs0.15Pb(I0.85Br0.15)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.71\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.5\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"18.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.17Cs0.83PbI2.2Br0.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.72\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.9\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1244.0\"}, {\"Refs.\": \"D. P. McMeekin, G. Sadoughi, W. Rehman, G. E. Eperon, M. Saliba, M. T. H\\u00f6rantner, A. Haghighirad, N. Sakai, L. Korte, B. Rech, M. B. Johnston, L. M. Herz, H. J. Snaith, Science 2016, 351, 151.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.83Cs0.17Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.72\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1200.0\"}, {\"Refs.\": \"T. Duong, H. Pham, T. C. Kho, P. Phang, K. C. Fong, D. Yan, Y. Yin, J. Peng, M. A. Mahmud, S. Gharibzadeh, B. A. Nejand, I. M. Hossain, M. R. Khan, N. Mozaffari, Y. Wu, H. Shen, J. Zheng, H. Mai, W. Liang, C. Samundsett, M. Stocks, K. McIntosh, G. G. Andersson, U. Lemmer, B. S. Richards, U. W. Paetzold, A. Ho-Ballie, Y. Liu, D. Macdonald, A. Blakers, J. Wong-Leung, T. White, K. Weber, K. Catchpole, Adv. Energy Mater. 2020, 10, 1903553.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Rb0.05Cs0.095MA0.1425FA0.7125PbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.3\", \"Jsc [mA cm\\u22122]\": \"18.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1269.0\"}, {\"Refs.\": \"S. Gharibzadeh, B. Abdollahi Nejand, M. Jakoby, T. Abzieher, D. Hauschild, S. Moghadamzadeh, J. A. Schwenzer, P. Brenner, R. Schmager, A. A. Haghighirad, L. Weinhardt, U. Lemmer, B. S. Richards, I. A. Howard, U. W. Paetzold, Adv. Energy Mater. 2019, 9, 1803699.\", \"PCE [%]\": \"19.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.83Cs0.17Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.75\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1310.0\"}, {\"Refs.\": \"Y. Lin, B. Chen, F. Zhao, X. Zheng, Y. Deng, Y. Shao, Y. Fang, Y. Bai, C. Wang, J. Huang, Adv. Mater. 2017, 29, 1700607.\", \"PCE [%]\": \"18.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.83MA0.17)0.95Cs0.05Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.76\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.4\", \"Jsc [mA cm\\u22122]\": \"20.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1210.0\"}, {\"Refs.\": \"Q. Ye, Y. Zhao, S. Mu, F. Ma, F. Gao, Z. Chu, Z. Yin, P. Gao, X. Zhang, J. You, Adv. Mater. 2019, 31, 1905143.\", \"PCE [%]\": \"18.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI3\\u2212xBrx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.5\", \"Jsc [mA cm\\u22122]\": \"18.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1234.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"15.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.17FA0.83Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.78\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.5\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1210.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"19.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.12MA0.05FA0.83Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"19.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1250.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"16.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.17Cs0.83PbI1.8Br1.2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.8\", \"Jsc [mA cm\\u22122]\": \"17.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1284.0\"}, {\"Refs.\": \"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\", \"PCE [%]\": \"13.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbBrI2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"14.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1272.0\"}, {\"Refs.\": \"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\", \"PCE [%]\": \"16.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.6Cs0.4Pb(I0.65Br0.35)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.6\", \"Jsc [mA cm\\u22122]\": \"17.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1220.0\"}, {\"Refs.\": \"Y.-N. Zhang, B. Li, L. Fu, Y. Zou, Q. Li, L.-W. Yin, Sol. Energy Mater. Sol. Cells 2019, 194, 168.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI1.5Br1.5/CsPbI1.5Br1.5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.0\", \"Jsc [mA cm\\u22122]\": \"21.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"M. Chen, M.-G. Ju, A. D. Carl, Y. Zong, R. L. Grimm, J. Gu, X. C. Zeng, Y. Zhou, N. P. Padture, Joule 2018, 2, 558.\", \"PCE [%]\": \"3.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs2TiBr6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.9\", \"Jsc [mA cm\\u22122]\": \"5.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"M.-J. Wu, C.-C. Kuo, L.-S. Jhuang, P.-H. Chen, Y.-F. Lai, F.-C. Chen, Adv. Energy Mater. 2019, 9, 1901863.\", \"PCE [%]\": \"8.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA0.85Cs0.15Pb(I0.65Br0.35)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.4\", \"Jsc [mA cm\\u22122]\": \"11.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8Pb(I0.6Br0.4)3-DAP\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.84\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1260.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"15.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.17Cs0.83PbI1.5Br1.5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1296.0\"}, {\"Refs.\": \"J. Zhang, Z. Wang, A. Mishra, M. Yu, M. Shasti, W. Tress, D. J. Kubicki, C. E. Avalos, H. Lu, Y. Liu, B. I. Carlsen, A. Agarwalla, Z. Wang, W. Xiang, L. Emsley, Z. Zhang, M. Gr\\u00e4tzel, W. Guo, A. Hagfeldt, Joule 2020, 4, 222.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb(I0.75Br0.25)3-0.5FAOAc\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.8\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1340.0\"}, {\"Refs.\": \"W. Xiang, Z. Wang, D. J. Kubicki, X. Wang, W. Tress, J. Luo, J. Zhang, A. Hofstetter, L. Zhang, L. Emsley, M. Gr\\u00e4tzel, A. Hagfeldt, Nat. Commun. 2019, 10, 4686.\", \"PCE [%]\": \"14.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb0.8Ba0.2I2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"14.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1280.0\"}, {\"Refs.\": \"W. Xiang, Z. Wang, D. J. Kubicki, W. Tress, J. Luo, D. Prochowicz, S. Akin, L. Emsley, J. Zhou, G. Dietler, M. Gr\\u00e4tzel, A. Hagfeldt, Joule 2019, 3, 205.\", \"PCE [%]\": \"13.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb0.95Eu0.05I2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.8\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1220.0\"}, {\"Refs.\": \"S. Yang, H. Zhao, Y. Han, C. Duan, Z. Liu, S. Liu, Small 2019, 15, 1904387.\", \"PCE [%]\": \"15.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1250.0\"}, {\"Refs.\": \"H. Zhao, Y. Han, Z. Xu, C. Duan, S. Yang, S. Yuan, Z. Yang, Z. Liu, S. Liu, Adv. Energy Mater. 2019, 9, 1902279.\", \"PCE [%]\": \"15.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2\\u2212xBr(A x\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.89\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.3\", \"Jsc [mA cm\\u22122]\": \"15.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1300.0\"}, {\"Refs.\": \"C. Duan, J. Cui, M. Zhang, Y. Han, S. Yang, H. Zhao, H. Bian, J. Yao, K. Zhao, Z. Liu, S. Liu, Adv. Energy Mater. 2020, 10, 2000691.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.9\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.7\", \"Jsc [mA cm\\u22122]\": \"15.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1320.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"14.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.17Cs0.83PbI1.2Br1.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.91\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1312.0\"}, {\"Refs.\": \"H. Bian, D. Bai, Z. Jin, K. Wang, L. Liang, H. Wang, J. Zhang, Q. Wang, S. Liu, Joule 2018, 2, 1500.\", \"PCE [%]\": \"13.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.91\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.9\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1177.0\"}, {\"Refs.\": \"K. M. Boopathi, P. Karuppuswamy, A. Singh, C. Hanmandlu, L. Lin, S. A. Abbas, C. C. Chang, P. C. Wang, G. Li, C. W. Chu, J. Mater. Chem. A 2017, 5, 20843.\", \"PCE [%]\": \"2.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA3Sb2I9+HI\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.91\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.8\", \"Jsc [mA cm\\u22122]\": \"5.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"620.0\"}, {\"Refs.\": \"I. Turkevych, S. Kazaoui, E. Ito, T. Urano, K. Yamada, H. Tomiyasu, H. Yamagishi, M. Kondo, S. Aramaki, ChemSusChem 2017, 10, 3754.\", \"PCE [%]\": \"4.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Ag3BiI6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.8\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\", \"PCE [%]\": \"2.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"AgBiI4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.7\", \"Jsc [mA cm\\u22122]\": \"5.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"670.0\"}, {\"Refs.\": \"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\", \"PCE [%]\": \"2.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"AgBiI5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.95\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.4\", \"Jsc [mA cm\\u22122]\": \"6.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"B.-W. Park, B. Philippe, X. Zhang, H. Rensmo, G. Boschloo, E. M. J. Johansson, Adv. Mater. 2015, 27, 6806.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs3Bi2I9\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.97\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.6\", \"Jsc [mA cm\\u22122]\": \"2.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"J. Liang, P. Zhao, C. Wang, Y. Wang, Y. Hu, G. Zhu, L. Ma, J. Liu, Z. Jin, J. Am. Chem. Soc. 2017, 139, 14009.\", \"PCE [%]\": \"8.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.98\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.0\", \"Jsc [mA cm\\u22122]\": \"12.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"D. Forg\\u00e1cs, L. Gil-Escrig, D. P\\u00e9rez-Del-Rey, C. Momblona, J. Werner, B. Niesen, C. Ballif, M. Sessolo, H. J. Bolink, Adv. Energy Mater. 2017, 7, 1602121.\", \"PCE [%]\": \"9.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.15FA0.85Pb(I0.3Br0.7)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1185.0\"}, {\"Refs.\": \"S. A. Kulkarni, T. Baikie, P. P. Boix, N. Yantara, N. Mathews, S. Mhaisalkar, J. Mater. Chem. A 2014, 2, 9221.\", \"PCE [%]\": \"2.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.41Br0.59)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.03\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.7\", \"Jsc [mA cm\\u22122]\": \"6.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"836.0\"}, {\"Refs.\": \"Q. Xue, G. Chen, M. Liu, J. Xiao, Z. Chen, Z. Hu, X.-F. Jiang, B. Zhang, F. Huang, W. Yang, H.-L. Yip, Y. Cao, Adv. Energy Mater. 2016, 6, 1502021.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.3Br0.7)xCl3\\u2212x(Br)\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.04\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"9.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1340.0\"}, {\"Refs.\": \"Y. Zhao, A. M. Nardes, K. Zhu, Faraday Discuss. 2014, 176, 301.\", \"PCE [%]\": \"6.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.1\", \"Jsc [mA cm\\u22122]\": \"5.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1450.0\"}, {\"Refs.\": \"H. Wang, S. Cao, B. Yang, H. Li, M. Wang, X. Hu, K. Sun, Z. Zang, Sol. RRL 2020, 4, 1900363.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.4\", \"Jsc [mA cm\\u22122]\": \"11.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1270.0\"}, {\"Refs.\": \"W. Zhu, Z. Zhang, W. Chai, Q. Zhang, D. Chen, Z. Lin, J. Chang, J. Zhang, C. Zhang, Y. Hao, ChemSusChem 2019, 12, 2318.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.1\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"11.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1261.0\"}, {\"Refs.\": \"B. Zhang, W. Bi, Y. Wu, C. Chen, H. Li, Z. Song, Q. Dai, L. Xu, H. Song, ACS Appl. Mater. Interfaces 2019, 11, 33868.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"GAI-DEE-CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.6\", \"Jsc [mA cm\\u22122]\": \"10.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1200.0\"}, {\"Refs.\": \"R. Nie, A. Mehta, B.-w. Park, H.-W. Kwon, J. Im, S. I. Seok, J. Am. Chem. Soc. 2018, 140, 872.\", \"PCE [%]\": \"3.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MASbSI2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.14\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.4\", \"Jsc [mA cm\\u22122]\": \"8.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\", \"PCE [%]\": \"4.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.85MA0.15Pb(I0.85Br0.15)3) R = 0.7\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.15\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.8\", \"Jsc [mA cm\\u22122]\": \"6.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1084.0\"}, {\"Refs.\": \"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\", \"PCE [%]\": \"2.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.85MA0.15Pb(I0.85Br0.15)3) R = 0.56\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.19\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.5\", \"Jsc [mA cm\\u22122]\": \"3.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1051.0\"}, {\"Refs.\": \"F. Umar, J. Zhang, Z. Jin, I. Muhammad, X. Yang, H. Deng, K. Jahangeer, Q. Hu, H. Song, J. Tang, Adv. Opt. Mater. 2019, 7, 1801368.\", \"PCE [%]\": \"1.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs3Sb2I9\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.2\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"55.9\", \"Jsc [mA cm\\u22122]\": \"3.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"610.0\"}, {\"Refs.\": \"Y. Zhang, Y. Liang, Y. Wang, F. Guo, L. Sun, D. Xu, ACS Energy Lett. 2018, 3, 1808.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.27\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.5\", \"Jsc [mA cm\\u22122]\": \"8.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1552.0\"}, {\"Refs.\": \"J. Duan, Y. Zhao, B. He, Q. Tang, Angew. Chem., Int. Ed. 2018, 57, 3787.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.9\", \"Jsc [mA cm\\u22122]\": \"8.12\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1458.0\"}, {\"Refs.\": \"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"7.72\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1653.0\"}, {\"Refs.\": \"G. Liao, J. Duan, Y. Zhao, Q. Tang, Sol. Energy 2018, 171, 279.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.1\", \"Jsc [mA cm\\u22122]\": \"7.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1470.0\"}, {\"Refs.\": \"J. Zhu, B. He, Z. Gong, Y. Ding, W. Zhang, X. Li, Z. Zong, H. Chen, Q. Tang, ChemSusChem 2020, 13, 1834.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.8\", \"Jsc [mA cm\\u22122]\": \"7.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1584.0\"}, {\"Refs.\": \"Y. Zhao, J. Duan, Y. Wang, X. Yang, Q. Tang, Nano Energy 2020, 67, 104286.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.5\", \"Jsc [mA cm\\u22122]\": \"7.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1622.0\"}, {\"Refs.\": \"Y. Zhao, J. Duan, H. Yuan, Y. Wang, X. Yang, B. He, Q. Tang, Sol. RRL 2019, 3, 1800284.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsSnBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.4\", \"Jsc [mA cm\\u22122]\": \"7.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1610.0\"}, {\"Refs.\": \"C. H. Ng, T. S. Ripolles, K. Hamada, S. H. Teo, H. N. Lim, J. Bisquert, S. Hayase, Sci. Rep. 2018, 8, 2482.\", \"PCE [%]\": \"4.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr2.9I0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.36\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.6\", \"Jsc [mA cm\\u22122]\": \"5.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1130.0\"}, {\"Refs.\": \"F. Jiang, D. Yang, Y. Jiang, T. Liu, X. Zhao, Y. Ming, B. Luo, F. Qin, J. Fan, H. Han, L. Zhang, Y. Zhou, J. Am. Chem. Soc. 2018, 140, 1019.\", \"PCE [%]\": \"2.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA3Sb2ClxI9\\u2212x\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.5\", \"Jsc [mA cm\\u22122]\": \"5.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"X. Wan, Z. Yu, W. Tian, F. Huang, S. Jin, X. Yang, Y.-B. Cheng, A. Hagfeldt, L. Sun, J. Energy Chem. 2020, 46, 8.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.8\", \"Jsc [mA cm\\u22122]\": \"6.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1490.0\"}, {\"Refs.\": \"Y. Zhao, H. Xu, Y. Wang, X. Yang, J. Duan, Q. Tang, J. Power Sources 2019, 440, 227151.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.91Rb0.09PbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"8.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1580.0\"}, {\"Refs.\": \"M. Safdari, P. H. Svensson, M. T. Hoang, I. Oh, L. Kloo, J. M. Gardner, J. Mater. Chem. A 2016, 4, 15638.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"BdAPbI4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"43.0\", \"Jsc [mA cm\\u22122]\": \"2.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"870.0\"}, {\"Refs.\": \"G. Murugadoss, R. Thangamuthu, S. M. Senthil Kumar, N. Anandhan, M. Rajesh Kumar, A. Rathishkumar, J. Alloys Compd. 2019, 787, 17.\", \"PCE [%]\": \"2.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb2Br5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.3\", \"Jsc [mA cm\\u22122]\": \"5.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"2.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbBr2.1Cl0.9\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.9\", \"Jsc [mA cm\\u22122]\": \"3.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"E. Greul, M. L. Petrus, A. Binek, P. Docampo, T. Bein, J. Mater. Chem. A 2017, 5, 19972.\", \"PCE [%]\": \"1.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs2AgBiBr6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"40.2\", \"Jsc [mA cm\\u22122]\": \"3.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"1.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbBr2Cl\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.48\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.0\", \"Jsc [mA cm\\u22122]\": \"2.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table2\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.2\", \"Jsc [mA cm\\u22122]\": \"24.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"X. Song, N. Gasparini, L. Ye, H. Yao, J. Hou, H. Ade, D. Baran, ACS Energy Lett. 2018, 3, 669.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.9\", \"Jsc [mA cm\\u22122]\": \"27.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"712.0\"}, {\"Refs.\": \"X. Song, N. Gasparini, M. M. Nahid, S. H. K. Paleti, C. Li, W. Li, H. Ade, D. Baran, Adv. Funct. Mater. 2019, 29, 1902441.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDTT-DPP:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.2\", \"Jsc [mA cm\\u22122]\": \"19.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"695.0\"}, {\"Refs.\": \"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\", \"PCE [%]\": \"14.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:BTP-4F:PC61BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.5\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"802.0\"}, {\"Refs.\": \"S. Liu, J. Yuan, W. Deng, M. Luo, Y. Xie, Q. Liang, Y. Zou, Z. He, H. Wu, Y. Cao, Nat. Photonics 2020, 14, 300.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y11\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.36\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"25.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"846.0\"}, {\"Refs.\": \"J. Yuan, Y. Zhang, L. Zhou, G. Zhang, H.-L. Yip, T.-K. Lau, X. Lu, C. Zhu, H. Peng, P. A. Johnson, M. Leclerc, Y. Cao, J. Ulanski, Y. Li, Y. Zou, Joule 2019, 3, 1140.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.6\", \"Jsc [mA cm\\u22122]\": \"26.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, J. Zhang, K. Xian, T. Zhang, L. Hong, Y. Wang, Y. Xu, K. Ma, C. An, C. He, Z. Wei, F. Gao, J. Hou, Adv. Mater. 2020, 32, 1908205.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-eC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.5\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"841.0\"}, {\"Refs.\": \"Q. Liu, Y. Jiang, K. Jin, J. Qin, J. Xu, W. Li, J. Xiong, J. Liu, Z. Xiao, K. Sun, S. Yang, X. Zhang, L. Ding, Sci. Bull. 2020, 65, 272.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"D18:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.6\", \"Jsc [mA cm\\u22122]\": \"27.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"859.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, L. Hong, T. Zhang, Y. Tang, B. Lin, K. Xian, B. Gao, C. An, P. Bi, W. Ma, J. Hou, Natl. Sci. Rev. 2019, 7, 1239.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-4Cl-12\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"25.5\", \"Jsc [mA cm\\u22122]\": \"77.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"858.0\"}, {\"Refs.\": \"Z. Zhou, W. Liu, G. Zhou, M. Zhang, D. Qian, J. Zhang, S. Chen, S. Xu, C. Yang, F. Gao, H. Zhu, F. Liu, X. Zhu, Adv. Mater. 2020, 32, 1906324.\", \"PCE [%]\": \"16.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:AQx-2\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.3\", \"Jsc [mA cm\\u22122]\": \"25.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"Y. Lin, B. Adilbekova, Y. Firdaus, E. Yengel, H. Faber, M. Sajjad, X. Zheng, E. Yarali, A. Seitkhan, O. M. Bakr, A. El-Labban, U. Schwingenschl\\u00f6gl, V. Tung, I. McCulloch, F. Laquai, T. D. Anthopoulos, Adv. Mater. 2019, 31, 1902965.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:Y6:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.8\", \"Jsc [mA cm\\u22122]\": \"26.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"L. Liu, Y. Kan, K. Gao, J. Wang, M. Zhao, H. Chen, C. Zhao, T. Jiu, A.-K.-Y. Jen, Y. Li, Adv. Mater. 2020, 32, 1907604.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"26.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"834.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\", \"PCE [%]\": \"16.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"25.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"867.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\", \"PCE [%]\": \"17.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.9\", \"Jsc [mA cm\\u22122]\": \"25.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"862.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\", \"PCE [%]\": \"15.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.1\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"834.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\", \"PCE [%]\": \"15.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.4\", \"Jsc [mA cm\\u22122]\": \"25.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"838.0\"}, {\"Refs.\": \"Q. Guo, J. Lin, H. Liu, X. Dong, X. Guo, L. Ye, Z. Ma, Z. Tang, H. Ade, M. Zhang, Y. Li, Nano Energy 2020, 74, 104861.\", \"PCE [%]\": \"14.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:IDST-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"H. Lai, Q. Zhao, Z. Chen, H. Chen, P. Chao, Y. Zhu, Y. Lang, N. Zhen, D. Mo, Y. Zhang, F. He, Joule 2020, 4, 688.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTIC-F-m\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.1\", \"Jsc [mA cm\\u22122]\": \"21.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"K. Jiang, Q. Wei, J. Y. L. Lai, Z. Peng, H. K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Joule 2019, 3, 3020.\", \"PCE [%]\": \"12.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:N-C11\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.6\", \"Jsc [mA cm\\u22122]\": \"21.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"852.0\"}, {\"Refs.\": \"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\", \"PCE [%]\": \"14.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:BP-4F:MF1\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.47\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"23.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"882.0\"}, {\"Refs.\": \"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:IDT-EDOT:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.48\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.7\", \"Jsc [mA cm\\u22122]\": \"20.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\", \"PCE [%]\": \"15.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:DTTC-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"22.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\", \"PCE [%]\": \"13.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:SeTlC4Cl-DIO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.51\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:IDT-EDOT:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"18.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:SeTlC4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.7\", \"Jsc [mA cm\\u22122]\": \"22.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTR:NITI:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.8\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.3\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"826.0\"}, {\"Refs.\": \"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\", \"PCE [%]\": \"13.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:DTTC-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.4\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"950.0\"}, {\"Refs.\": \"Y. Lin, B. Adilbekova, Y. Firdaus, E. Yengel, H. Faber, M. Sajjad, X. Zheng, E. Yarali, A. Seitkhan, O. M. Bakr, A. El-Labban, U. Schwingenschl\\u00f6gl, V. Tung, I. McCulloch, F. Laquai, T. D. Anthopoulos, Adv. Mater. 2019, 31, 1902965.\", \"PCE [%]\": \"13.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-SF:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.53\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\", \"PCE [%]\": \"13.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:DTC-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.5\", \"Jsc [mA cm\\u22122]\": \"20.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:MF1\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"916.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.5\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"793.0\"}, {\"Refs.\": \"Z. Luo, C. Sun, S. Chen, Z.-G. Zhang, K. Wu, B. Qiu, C. Yang, Y. Li, C. Yang, Adv. Energy Mater. 2018, 8, 1800856.\", \"PCE [%]\": \"12.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTQ10:IDTPC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"930.0\"}, {\"Refs.\": \"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTQ10:IDIC-2F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.6\", \"Jsc [mA cm\\u22122]\": \"19.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"910.0\"}, {\"Refs.\": \"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\", \"PCE [%]\": \"12.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTQ10:IDIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.3\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\", \"PCE [%]\": \"9.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"J51:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.7\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.2\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"815.0\"}, {\"Refs.\": \"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"P4TIF:PC61BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.9\", \"Jsc [mA cm\\u22122]\": \"21.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2016, 24, 3.\", \"PCE [%]\": \"11.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.7\", \"Jsc [mA cm\\u22122]\": \"19.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"791.0\"}, {\"Refs.\": \"D. Baran, N. Gasparini, A. Wadsworth, C. H. Tan, N. Wehbe, X. Song, Z. Hamid, W. Zhang, M. Neophytou, T. Kirchartz, C. J. Brabec, J. R. Durrant, I. McCulloch, Nat. Commun. 2018, 9, 2059.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDTTT-EFT:EHIDTBR\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"18.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"C. Li, J. Song, Y. Cai, G. Han, W. Zheng, Y. Yi, H. S. Ryu, H. Y. Woo, Y. Sun, J. Energy Chem. 2020, 40, 144.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBT1-C:NFA\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.9\", \"Jsc [mA cm\\u22122]\": \"13.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"878.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\", \"PCE [%]\": \"11.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"867.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.72\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.4\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"899.0\"}, {\"Refs.\": \"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BDT-ffBX-DT:PDI4\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.1\", \"Jsc [mA cm\\u22122]\": \"10.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\", \"PCE [%]\": \"6.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BDT-ffBX-DT:SFPDI\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.6\", \"Jsc [mA cm\\u22122]\": \"8.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1230.0\"}, {\"Refs.\": \"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\", \"PCE [%]\": \"9.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTR:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.9\", \"Jsc [mA cm\\u22122]\": \"13.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"900.0\"}, {\"Refs.\": \"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\", \"PCE [%]\": \"7.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.1\", \"Jsc [mA cm\\u22122]\": \"13.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"M. Li, H. Wang, Y. Liu, Y. Zhou, H. Lu, J. Song, Z. Bo, Dyes Pigm. 2020, 175, 108186.\", \"PCE [%]\": \"7.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:NDP-Se-DIO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.9\", \"Jsc [mA cm\\u22122]\": \"12.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\", \"PCE [%]\": \"5.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:PC61BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"55.9\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"950.0\"}, {\"Refs.\": \"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\", \"PCE [%]\": \"3.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"P3HT:PCBM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.2\", \"Jsc [mA cm\\u22122]\": \"10.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"592.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \" \", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.3\", \"Jsc [mA cm\\u22122]\": \"21.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"714.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\", \"PCE [%]\": \"11.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \" \", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"21.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"743.0\"}, {\"Refs.\": \"T.-K. Chang, Y. Chi, RSC Adv. 2017, 7, 42013.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"TF-tBu_C3F7\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.9\", \"Jsc [mA cm\\u22122]\": \"18.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"YD2\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.7\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"694.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"740.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"SK7\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.5\", \"Jsc [mA cm\\u22122]\": \"13.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"663.0\"}, {\"Refs.\": \"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\", \"PCE [%]\": \"6.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"AN-11\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.8\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \" \", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"15.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"8.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"14.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"782.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"L351\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.7\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"TY4\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"730.0\"}, {\"Refs.\": \"X. Wang, A. Bolag, W. Yun, Y. Du, C. Eerdun, X. Zhang, T. Bao, J. Ning, H. Alata, T. Ojiyed, J. Mol. Struct. 2020, 1206, 127694.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719+W2\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.89\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.8\", \"Jsc [mA cm\\u22122]\": \"21.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"580.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"L350\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.93\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"13.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\", \"PCE [%]\": \"3.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"AN-14\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.97\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"6.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"600.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"5.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"SK6\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.99\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.5\", \"Jsc [mA cm\\u22122]\": \"11.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"689.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"6.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"CW10+SK6\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"12.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"732.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"L349\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.1\", \"Jsc [mA cm\\u22122]\": \"11.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1160.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"TY6\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.02\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\", \"PCE [%]\": \"3.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"AN-12\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"7.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"TY3\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.3\", \"Jsc [mA cm\\u22122]\": \"11.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"5.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"CW10\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.12\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.7\", \"Jsc [mA cm\\u22122]\": \"10.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"739.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"5.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"MS3\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.8\", \"Jsc [mA cm\\u22122]\": \"10.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321\", \"PCE [%]\": \"5.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"L348\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"6.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"T. K. Todorov, J. Tang, S. Bag, O. Gunawan, T. Gokmen, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2013, 3, 34.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.6\", \"Jsc [mA cm\\u22122]\": \"38.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"447.0\"}, {\"Refs.\": \"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcob\\u00e9, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. P\\u00e9rez-Rodr\\u00edguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\", \"PCE [%]\": \"9.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.3\", \"Jsc [mA cm\\u22122]\": \"32.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"457.0\"}, {\"Refs.\": \"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcob\\u00e9, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. P\\u00e9rez-Rodr\\u00edguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\", \"PCE [%]\": \"9.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.12\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.4\", \"Jsc [mA cm\\u22122]\": \"31.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"460.0\"}, {\"Refs.\": \"W. Wang, M. T. Winkler, O. Gunawan, T. Gokmen, T. K. Todorov, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2014, 4, 1301465.\", \"PCE [%]\": \"12.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.13\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.8\", \"Jsc [mA cm\\u22122]\": \"35.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"513.0\"}, {\"Refs.\": \"T. K. Todorov, J. Tang, S. Bag, O. Gunawan, T. Gokmen, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2013, 3, 34.\", \"PCE [%]\": \"11.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.13\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.8\", \"Jsc [mA cm\\u22122]\": \"34.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"460.0\"}, {\"Refs.\": \"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcob\\u00e9, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. P\\u00e9rez-Rodr\\u00edguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\", \"PCE [%]\": \"8.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.15\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.7\", \"Jsc [mA cm\\u22122]\": \"30.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"426.0\"}, {\"Refs.\": \"K. Shen, Y. Zhang, X. Wang, C. Ou, F. Guo, H. Zhu, C. Liu, Y. Gao, R. E. I. Schropp, Z. Li, X. Liu, Y. Mai, Adv. Sci. 2020, 7, 2001013.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.22\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.4\", \"Jsc [mA cm\\u22122]\": \"28.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"413.0\"}, {\"Refs.\": \"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.24\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.6\", \"Jsc [mA cm\\u22122]\": \"32.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"400.0\"}, {\"Refs.\": \"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\", \"PCE [%]\": \"4.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.27\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"47.3\", \"Jsc [mA cm\\u22122]\": \"27.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"370.0\"}, {\"Refs.\": \"C. Yan, J. Huang, K. Sun, S. Johnston, Y. Zhang, H. Sun, A. Pu, M. He, F. Liu, K. Eder, L. Yang, J. M. Cairney, N. J. Ekins-Daukes, Z. Hameiri, J. A. Stride, S. Chen, M. A. Green, X. Hao, Nat. Energy 2018, 3, 764.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnS4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.3\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"731.0\"}, {\"Refs.\": \"R. Tang, X. Wang, W. Lian, J. Huang, Q. Wei, M. Huang, Y. Yin, C. Jiang, S. Yang, G. Xing, S. Chen, C. Zhu, X. Hao, M. A. Green, T. Chen, Nat. Energy 2020, 5, 587.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2(S,Se)3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.3\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"655.0\"}, {\"Refs.\": \"K. Timmo, M. Altosaar, M. Pilvet, V. Mikli, M. Grossberg, M. Danilson, T. Raadik, R. Josepson, J. Krustok, M. Kauk-Kuusik, J. Mater. Chem. A 2019, 7, 24281.\", \"PCE [%]\": \"8.73\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"(Cu0.99Ag0.01)1.85(Zn0.8Cd0.2)1.1SnS4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.9\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"664.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2014, 22, 1.\", \"PCE [%]\": \"19.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"34.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"716.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\", \"PCE [%]\": \"21.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.1\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.3\", \"Jsc [mA cm\\u22122]\": \"40.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"718.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\", \"PCE [%]\": \"26.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (crystalline)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.9\", \"Jsc [mA cm\\u22122]\": \"42.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"738.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2018, 26, 427.\", \"PCE [%]\": \"22.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.13\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.5\", \"Jsc [mA cm\\u22122]\": \"38.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"744.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 805.\", \"PCE [%]\": \"21.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.14\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"35.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"757.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\", \"PCE [%]\": \"23.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.15\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.4\", \"Jsc [mA cm\\u22122]\": \"39.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"734.0\"}, {\"Refs.\": \"W. Li, S. Xu, Y. Dai, P. Ma, Y. Feng, W. Li, H. Luo, C. Yang, Mater. Lett. 2019, 244, 43.\", \"PCE [%]\": \"16.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.1\", \"Jsc [mA cm\\u22122]\": \"31.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"762.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics Res. Appl. 2019, 27, 3.\", \"PCE [%]\": \"29.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"GaAs\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"86.7\", \"Jsc [mA cm\\u22122]\": \"29.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1127.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\", \"PCE [%]\": \"21.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"30.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1062.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.48\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"27.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"857.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (amorphous)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.8\", \"Jsc [mA cm\\u22122]\": \"16.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"896.0\"}, {\"Refs.\": \"T. Matsui, A. Bidiville, K. Maejima, H. Sai, T. Koida, T. Suezaki, M. Matsumoto, K. Saito, I. Yoshida, M. Kondo, Appl. Phys. Lett. 2015, 106, 053901.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (amorphous)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"16.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"896.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, Prog. Photovoltaics 2010, 18, 346.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (amorphous)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.0\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"886.0\"}, {\"Refs.\": \"M. Ma, Q. Tang, H. Chen, B. He, P. Yang, Sol. Energy Mater. Sol. Cells 2017, 160, 67.\", \"PCE [%]\": \"3.62\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(5-AVA)y(MA)1\\u2212yPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.47\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"40.6\", \"Jsc [mA cm\\u22122]\": \"14.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"616.0\"}, {\"Refs.\": \"D. Yang, R. Yang, K. Wang, C. Wu, X. Zhu, J. Feng, X. Ren, G. Fang, S. Priya, S. Liu, Nat. Commun. 2018, 9, 3239.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.95Cs0.05PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.5\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"J. H. Heo, D. H. Shin, D. H. Song, D. H. Kim, S. J. Lee, S. H. Im, J. Mater. Chem. A 2018, 6, 8251.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI3 xBrx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.9\", \"Jsc [mA cm\\u22122]\": \"22.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"C. Wang, L. Guan, D. Zhao, Y. Yu, C. R. Grice, Z. Song, R. A. Awni, J. Chen, J. Wang, X. Zhao, Y. Yan, ACS Energy Lett. 2017, 2, 2118.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA0.7FA0.3PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.4\", \"Jsc [mA cm\\u22122]\": \"22.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1101.0\"}, {\"Refs.\": \"K. Huang, Y. Peng, Y. Gao, J. Shi, H. Li, X. Mo, H. Huang, Y. Gao, L. Ding, J. Yang, Adv. Energy Mater. 2019, 9, 1901419.\", \"PCE [%]\": \"19.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.945MA0.025Cs0.03Pb(I0.975Br0.025)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.0\", \"Jsc [mA cm\\u22122]\": \"23.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"X. Dai, Y. Deng, C. H. Van Brackle, S. Chen, P. N. Rudd, X. Xiao, Y. Lin, B. Chen, J. Huang, Adv. Energy Mater. 2020, 10, 1903108.\", \"PCE [%]\": \"19.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3 NH4Cl\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"22.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"Z. Wang, L. Zeng, C. Zhang, Y. Lu, S. Qiu, C. Wang, C. Liu, L. Pan, S. Wu, J. Hu, G. Liang, P. Fan, H.-J. Egelhaaf, C. J. Brabec, F. Guo, Y. Mai, Adv. Funct. Mater. 2020, 30, 2001240.\", \"PCE [%]\": \"19.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"21.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"J. Feng, X. Zhu, Z. Yang, X. Zhang, J. Niu, Z. Wang, S. Zuo, S. Priya, S. Liu, D. Yang, Adv. Mater. 2018, 30, 1801418.\", \"PCE [%]\": \"18.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3 dimethylsulfide\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"22.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1103.0\"}, {\"Refs.\": \"C. Liu, L. Zhang, X. Zhou, J. Gao, W. Chen, X. Wang, B. Xu, Adv. Funct. Mater. 2019, 29, 1807604.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.81MA0.14PbI2.55Br0.45\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.9\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1062.0\"}, {\"Refs.\": \"B. Cao, L. Yang, S. Jiang, H. Lin, N. Wang, X. Li, J. Mater. Chem. A 2019, 7, 4960.\", \"PCE [%]\": \"19.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Rb0.01K0.04 (Cs0.05(FA0.83MA0.17)0.95)0.95(I0.83Br0.17)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"21.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1135.0\"}, {\"Refs.\": \"D. Xin, S. Tie, X. Zheng, J. Zhu, W.-H. Zhang, J. Energy Chem. 2020, 46, 173.\", \"PCE [%]\": \"18.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.06FA0.79MA0.15PbI2.55Br0.45\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.1\", \"Jsc [mA cm\\u22122]\": \"22.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"M. Gao, X. Han, X. Zhan, P. Liu, Y. Shan, Y. Chen, J. Li, R. Zhang, S. Wang, Q. Zhang, Y. Zheng, L. Chen, Mater. Lett. 2019, 248, 16.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.85(MAPbBr3)0.15\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.8\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.9\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"J. Xi, Z. Wu, K. Xi, H. Dong, B. Xia, T. Lei, F. Yuan, W. Wu, B. Jiao, X. Hou, Nano Energy 2016, 26, 438.\", \"PCE [%]\": \"7.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(\\u03b1-FAPbI3)0.5(MAPbI2Br)0.5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.7\", \"Jsc [mA cm\\u22122]\": \"10.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.2\", \"Jsc [mA cm\\u22122]\": \"24.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"W. Zhang, W. Song, J. Huang, L. Huang, T. Yan, J. Ge, R. Peng, Z. Ge, J. Mater. Chem. A 2019, 7, 22021.\", \"PCE [%]\": \"13.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"23.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"829.0\"}, {\"Refs.\": \"X. Chen, G. Xu, G. Zeng, H. Gu, H. Chen, H. Xu, H. Yao, Y. Li, J. Hou, Y. Li, Adv. Mater. 2020, 32, 1908478.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"25.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"832.0\"}, {\"Refs.\": \"T. Yan, W. Song, J. Huang, R. Peng, L. Huang, Z. Ge, Adv. Mater. 2019, 31, 1902210.\", \"PCE [%]\": \"14.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"23.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"828.0\"}, {\"Refs.\": \"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.3\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"X. Dong, P. Shi, L. Sun, J. Li, F. Qin, S. Xiong, T. Liu, X. Jiang, Y. Zhou, J. Mater. Chem. A 2019, 7, 1989.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.2\", \"Jsc [mA cm\\u22122]\": \"19.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"826.0\"}, {\"Refs.\": \"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\", \"PCE [%]\": \"10.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.8\", \"Jsc [mA cm\\u22122]\": \"18.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"900.0\"}, {\"Refs.\": \"Y. Yang, J. Ou, X. Lv, C. Meng, Y. Mai, Sol. Energy 2019, 180, 57.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"16.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\", \"PCE [%]\": \"9.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"J51:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.7\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"T. Xu, C. Gong, S. Wang, H. Lian, W. Lan, G. L\\u00e9v\\u00eaque, B. Grandidier, J. Plain, R. Bachelot, B. Wei, F. Zhu, Sol. RRL 2020, 4, 1900522.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.6\", \"Jsc [mA cm\\u22122]\": \"13.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\", \"PCE [%]\": \"3.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"P3HT:PCBM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.2\", \"Jsc [mA cm\\u22122]\": \"10.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"592.0\"}, {\"Refs.\": \"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\", \"PCE [%]\": \"4.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.0\", \"Jsc [mA cm\\u22122]\": \"10.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table9\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"T. Yamaguchi, N. Tobe, D. Matsumoto, T. Nagai, H. Arakawa, Sol. Energy Mater. Sol. Cells 2010, 94, 812.\", \"PCE [%]\": \"7.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.75\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.2\", \"Jsc [mA cm\\u22122]\": \"15.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table9\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"732.0\"}, {\"Refs.\": \"Y. Wang, P. Cheng, C. Feng, H. Zhang, W. Zhao, Sol. Energy 2019, 180, 423.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"13.19\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table9\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"729.0\"}, {\"Refs.\": \"H. Lee, J. Kim, D. Y. Kim, Y. Seo, Org. Electron. 2018, 52, 103.\", \"PCE [%]\": \"6.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"(JH-1)0.6(SQ2)0.4\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.9\", \"Jsc [mA cm\\u22122]\": \"12.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table9\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"754.0\"}, {\"Refs.\": \"Y. Xiao, J. Wu, G. Yue, J. Lin, M. Huang, Z. Lan, Electrochim. Acta 2011, 56, 8545.\", \"PCE [%]\": \"6.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.0\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table9\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"L. Song, Y. Guan, P. Du, Y. Yang, F. Ko, J. Xiong, Sol. Energy Mater. Sol. Cells 2016, 147, 134.\", \"PCE [%]\": \"4.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.2\", \"Jsc [mA cm\\u22122]\": \"10.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table9\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\", \"PCE [%]\": \"6.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.99\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"53.4\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table9\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"660.0\"}, {\"Refs.\": \"Q. Tang, H. Shen, H. Yao, K. Gao, Y. Jiang, Y. Li, Y. Liu, L. Zhang, Z. Ni, Q. Wei, Renewable Energy 2019, 133, 883.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"c-Si\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.14\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"36.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"656.0\"}, {\"Refs.\": \"A. Chiril\\u0103, P. Reinhard, F. Pianezzi, P. Bloesch, A. R. Uhl, C. Fella, L. Kranz, D. Keller, C. Gretener, H. Hagendorfer, D. Jaeger, R. Erni, S. Nishiwaki, S. Buecheler, A. N. Tiwari, Nat. Mater. 2013, 12, 1107.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.2\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"35.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"736.0\"}, {\"Refs.\": \"R. Kaczynski, J. Lee, J. V. Alsburg, B. Sang, U. Schoop, J. Britt, presented at 2017 IEEE 44th Photovoltaic Specialist Conf. (PVSC), June 2017.\", \"PCE [%]\": \"18.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.22\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.4\", \"Jsc [mA cm\\u22122]\": \"35.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"K. Ruan, K. Ding, Y. Wang, S. Diao, Z. Shao, X. Zhang, J. Jie, J. Mater. Chem. A 2015, 3, 14370.\", \"PCE [%]\": \"8.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"c-Si\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"24.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"550.0\"}, {\"Refs.\": \"S. Moon, K. Kim, Y. Kim, J. Heo, J. Lee, Sci. Rep. 2016, 6, 30107.\", \"PCE [%]\": \"22.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"GaAs\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.4\", \"Jsc [mA cm\\u22122]\": \"27.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"980.0\"}, {\"Refs.\": \"H. P. Mahabaduge, W. L. Rance, J. M. Burst, M. O. Reese, D. M. Meysing, C. A. Wolden, J. Li, J. D. Beach, T. A. Gessert, W. K. Metzger, S. Garner, T. M. Barnes, Appl. Phys. Lett. 2015, 106, 133501.\", \"PCE [%]\": \"16.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.4\", \"Jsc [mA cm\\u22122]\": \"25.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"831.0\"}, {\"Refs.\": \"L. Kranz, C. Gretener, J. Perrenoud, R. Schmitt, F. Pianezzi, F. La Mattina, P. Bl\\u00f6sch, E. Cheah, A. Chiril\\u0103, C. M. Fella, H. Hagendorfer, T. J\\u00e4ger, S. Nishiwaki, A. R. Uhl, S. Buecheler, A. N. Tiwari, Nat. Commun. 2013, 4, 2306.\", \"PCE [%]\": \"11.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.49\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.9\", \"Jsc [mA cm\\u22122]\": \"22.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"821.0\"}, {\"Refs.\": \"T. S\\u00f6derstr\\u00f6m, F.-J. Haug, V. Terrazzoni-Daudrix, C. Ballif, J. Appl. Phys. 2008, 103, 114509.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"a-Si:H\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"888.0\"}, {\"Refs.\": \"C. Zhang, Y. Song, M. Wang, M. Yin, X. Zhu, L. Tian, H. Wang, X. Chen, Z. Fan, L. Lu, D. Li, Adv. Funct. Mater. 2017, 27, 1604720.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"a-Si:H\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.0\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\", \"PCE [%]\": \"12.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"3.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.5\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1017.0\"}, {\"Refs.\": \"B. Chen, Y. Bai, Z. Yu, T. Li, X. Zheng, Q. Dong, L. Shen, M. Boccard, A. Gruverman, Z. Holman, J. Huang, Adv. Energy Mater. 2016, 6, 1601128.\", \"PCE [%]\": \"16.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"P. You, Z. Liu, Q. Tai, S. Liu, F. Yan, Adv. Mater. 2015, 27, 3632.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.3\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.9\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"J. H. Heo, H. J. Han, M. Lee, M. Song, D. H. Kim, S. H. Im, Energy Environ. Sci. 2015, 8, 2922.\", \"PCE [%]\": \"15.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"6.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.4\", \"Jsc [mA cm\\u22122]\": \"19.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"7.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.5\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"988.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"17.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.1\", \"Jsc [mA cm\\u22122]\": \"22.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.5\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"12.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.8\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"14.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"13.0\", \"Absorber\": \"MAPbI2.5Br0.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.4\", \"Jsc [mA cm\\u22122]\": \"19.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"13.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.9\", \"Jsc [mA cm\\u22122]\": \"19.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"11.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"15.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.3\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"13.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"16.0\", \"Absorber\": \"MAPbI2Br\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.76\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.4\", \"Jsc [mA cm\\u22122]\": \"16.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"16.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1040.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"12.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"MAPbI2Br\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.7\", \"Jsc [mA cm\\u22122]\": \"15.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.5\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1017.0\"}, {\"Refs.\": \"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.3\", \"Jsc [mA cm\\u22122]\": \"13.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"941.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"14.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.2\", \"Jsc [mA cm\\u22122]\": \"17.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1108.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"14.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"21.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.2\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1117.0\"}, {\"Refs.\": \"C.-Y. Chang, Y.-C. Chang, W.-K. Huang, K.-T. Lee, A.-C. Cho, C.-C. Hsu, Chem. Mater. 2015, 27, 7119.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"21.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.2\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"22.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"17.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1073.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.6\", \"Jsc [mA cm\\u22122]\": \"17.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1082.0\"}, {\"Refs.\": \"S. Xiao, H. Chen, F. Jiang, Y. Bai, Z. Zhu, T. Zhang, X. Zheng, G. Qian, C. Hu, Y. Zhou, Y. Qu, S. Yang, Adv. Mater. Interfaces 2016, 3, 1600484.\", \"PCE [%]\": \"11.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"15.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1040.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.4\", \"Jsc [mA cm\\u22122]\": \"17.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"9.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"24.0\", \"Absorber\": \"MAPbI1.5Br1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.6\", \"Jsc [mA cm\\u22122]\": \"13.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"C.-Y. Chang, K.-T. Lee, W.-K. Huang, H.-Y. Siao, Y.-C. Chang, Chem. Mater. 2015, 27, 5122.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.7\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"950.0\"}, {\"Refs.\": \"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"26.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"12.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"27.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.2\", \"Jsc [mA cm\\u22122]\": \"18.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"F. Guo, H. Azimi, Y. Hou, T. Przybilla, M. Hu, C. Bronnbauer, S. Langner, E. Spiecker, K. Forberich, C. J. Brabec, Nanoscale 2015, 7, 1642.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"964.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.2\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.9\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\", \"PCE [%]\": \"7.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.2\", \"Jsc [mA cm\\u22122]\": \"11.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1010.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"11.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"31.0\", \"Absorber\": \"MAPbI2.5Br0.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.4\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1050.0\"}, {\"Refs.\": \"C. Rold\\u00e1n-Carmona, O. Malinkiewicz, R. Betancur, G. Longo, C. Momblona, F. Jaramillo, L. Camacho, H. J. Bolink, Energy Environ. Sci. 2014, 7, 2968.\", \"PCE [%]\": \"7.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"33.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.5\", \"Jsc [mA cm\\u22122]\": \"13.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1037.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"11.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"34.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.6\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"990.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"36.0\", \"Absorber\": \"MAPbI2Br\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.5\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.1\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1010.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.6\", \"Jsc [mA cm\\u22122]\": \"11.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"38.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"13.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"41.0\", \"Absorber\": \"MAPbI1.5Br1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.9\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.2\", \"Jsc [mA cm\\u22122]\": \"12.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"42.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"13.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"45.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"12.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"3.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"46.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.4\", \"Jsc [mA cm\\u22122]\": \"5.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"S. Bag, M. F. Durstock, Nano Energy 2016, 30, 542.\", \"PCE [%]\": \"4.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"47.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"8.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"66.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.9\", \"Jsc [mA cm\\u22122]\": \"2.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"68.0\", \"Absorber\": \"FAPbBr2.43Cl0.57\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"6.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1550.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"72.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.3\", \"Jsc [mA cm\\u22122]\": \"2.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\", \"PCE [%]\": \"0.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"72.0\", \"Absorber\": \"MAPbCl3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"3.03\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"35.4\", \"Jsc [mA cm\\u22122]\": \"0.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"73.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.1\", \"Jsc [mA cm\\u22122]\": \"2.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\", \"PCE [%]\": \"0.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"73.0\", \"Absorber\": \"MAPbCl2.4Br0.6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.84\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"44.9\", \"Jsc [mA cm\\u22122]\": \"0.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1260.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"74.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.1\", \"Jsc [mA cm\\u22122]\": \"2.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\", \"PCE [%]\": \"7.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"2.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDTTT-C-T:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.3\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\", \"PCE [%]\": \"14.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"23.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"854.0\"}, {\"Refs.\": \"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"11.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDTTT-C-T:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.4\", \"Jsc [mA cm\\u22122]\": \"14.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\", \"PCE [%]\": \"13.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"13.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"853.0\"}, {\"Refs.\": \"T. Xiao, J. Wang, S. Yang, Y. Zhu, D. Li, Z. Wang, S. Feng, L. Bu, X. Zhan, G. Lu, J. Mater. Chem. A 2020, 8, 401.\", \"PCE [%]\": \"11.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FNIC2\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.3\", \"Jsc [mA cm\\u22122]\": \"21.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"727.0\"}, {\"Refs.\": \"T. Xiao, J. Wang, S. Yang, Y. Zhu, D. Li, Z. Wang, S. Feng, L. Bu, X. Zhan, G. Lu, J. Mater. Chem. A 2020, 8, 401.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"15.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FNIC1\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"18.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"772.0\"}, {\"Refs.\": \"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\", \"PCE [%]\": \"12.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T-2F:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.2\", \"Jsc [mA cm\\u22122]\": \"21.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\", \"PCE [%]\": \"11.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T-2F:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.6\", \"Jsc [mA cm\\u22122]\": \"20.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.4\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"852.0\"}, {\"Refs.\": \"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\", \"PCE [%]\": \"10.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"21.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T-2F:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.3\", \"Jsc [mA cm\\u22122]\": \"19.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"800.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FOIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.3\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"736.0\"}, {\"Refs.\": \"Y. Bai, C. Zhao, X. Chen, S. Zhang, S. Zhang, T. Hayat, A. Alsaedi, Z. a. Tan, J. Hou, Y. Li, J. Mater. Chem. A 2019, 7, 15887.\", \"PCE [%]\": \"12.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"26.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T-2F:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.4\", \"Jsc [mA cm\\u22122]\": \"21.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"825.0\"}, {\"Refs.\": \"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\", \"PCE [%]\": \"5.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDTTT-C-T:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.9\", \"Jsc [mA cm\\u22122]\": \"11.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"R. Xia, C. J. Brabec, H.-L. Yip, Y. Cao, Joule 2019, 3, 2241.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.7\", \"Jsc [mA cm\\u22122]\": \"21.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"718.0\"}, {\"Refs.\": \"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"34.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FOIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.1\", \"Jsc [mA cm\\u22122]\": \"18.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"733.0\"}, {\"Refs.\": \"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"36.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:BT-CIC:TT-FIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"18.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"36.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.5\", \"Jsc [mA cm\\u22122]\": \"11.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"6.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"10.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"4.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"39.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.9\", \"Jsc [mA cm\\u22122]\": \"8.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"43.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.1\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"730.0\"}, {\"Refs.\": \"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\", \"PCE [%]\": \"8.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"44.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:BT-CIC:TT-FIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.6\", \"Jsc [mA cm\\u22122]\": \"16.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"46.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.6\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. USA 2020, 117, 21147.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"47.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"730.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"2.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"47.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"4.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\", \"PCE [%]\": \"7.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"49.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:BT-CIC:TT-FIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.6\", \"Jsc [mA cm\\u22122]\": \"14.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"670.0\"}, {\"Refs.\": \"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\", \"PCE [%]\": \"8.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"50.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FOIC:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"16.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"746.0\"}, {\"Refs.\": \"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\", \"PCE [%]\": \"7.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"51.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7:FOIC:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.7\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"749.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"1.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"53.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"54.8\", \"Jsc [mA cm\\u22122]\": \"3.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\", \"PCE [%]\": \"5.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"53.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"DPP2T:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.5\", \"Jsc [mA cm\\u22122]\": \"10.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\", \"PCE [%]\": \"3.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"60.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"DPP2T:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.2\", \"Jsc [mA cm\\u22122]\": \"7.34\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"749.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"62.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:6TIC-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.0\", \"Jsc [mA cm\\u22122]\": \"12.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"C. Yang, M. Moemeni, M. Bates, W. Sheng, B. Borhan, R. R. Lunt, Adv. Opt. Mater. 2020, 8, 1901536.\", \"PCE [%]\": \"1.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"73.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"COi8DFIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.0\", \"Jsc [mA cm\\u22122]\": \"1.54\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"990.0\"}, {\"Refs.\": \"Y. Zhao, R. R. Lunt, Adv. Energy Mater. 2013, 3, 1143.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"84.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBMMA:PEMA:(TBA)2Mo6Cl14\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.0\", \"Jsc [mA cm\\u22122]\": \"1.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"520.0\"}, {\"Refs.\": \"Y. Zhao, G. A. Meek, B. G. Levine, R. R. Lunt, Adv. Opt. Mater. 2014, 2, 606.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"86.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"Cy7\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.0\", \"Jsc [mA cm\\u22122]\": \"1.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"500.0\"}, {\"Refs.\": \"C. L\\u00f3pez-L\\u00f3pez, S. Colodrero, H. M\\u00edguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\", \"PCE [%]\": \"5.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"1.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"53.7\", \"Jsc [mA cm\\u22122]\": \"12.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"C. L\\u00f3pez-L\\u00f3pez, S. Colodrero, H. M\\u00edguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\", \"PCE [%]\": \"4.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.0\", \"Jsc [mA cm\\u22122]\": \"10.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"4.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719+SDA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.0\", \"Jsc [mA cm\\u22122]\": \"9.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"5.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.0\", \"Jsc [mA cm\\u22122]\": \"11.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"C. L\\u00f3pez-L\\u00f3pez, S. Colodrero, H. M\\u00edguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\", \"PCE [%]\": \"4.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.1\", \"Jsc [mA cm\\u22122]\": \"11.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"765.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"13.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"SGT-021\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"14.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"851.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"9.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"SGT-021\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.5\", \"Jsc [mA cm\\u22122]\": \"14.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"9.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"15.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"SGT-021\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.2\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"9.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"SGT-021\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.5\", \"Jsc [mA cm\\u22122]\": \"15.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"855.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"4.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719+SDA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.0\", \"Jsc [mA cm\\u22122]\": \"9.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"3.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"8.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"C. L\\u00f3pez-L\\u00f3pez, S. Colodrero, H. M\\u00edguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\", \"PCE [%]\": \"3.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"24.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.9\", \"Jsc [mA cm\\u22122]\": \"7.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"786.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"2.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719+SDA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.0\", \"Jsc [mA cm\\u22122]\": \"5.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"1.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"N719\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.19\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"3.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"K. Kim, S. K. Nam, J. H. Moon, ACS Appl. Energy Mater. 2020, 3, 5277.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"43.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PdTPBP/BPEA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.95\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"15.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"2.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.9\", \"Jsc [mA cm\\u22122]\": \"23.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"9.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"K. Kim, W. N. Shafarman, Nano Energy 2016, 30, 488.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"46.5\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"597.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"16.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.3\", \"Jsc [mA cm\\u22122]\": \"14.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.3\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-SiGe:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.3\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.6\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.5\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"580.0\"}, {\"Refs.\": \"S. H. Moon, S. J. Park, Y. J. Hwang, D.-K. Lee, Y. Cho, D.-W. Kim, B. K. Min, Sci. Rep. 2014, 4, 4408.\", \"PCE [%]\": \"1.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"40.8\", \"Jsc [mA cm\\u22122]\": \"8.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"495.0\"}, {\"Refs.\": \"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\", \"PCE [%]\": \"5.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"22.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.6\", \"Jsc [mA cm\\u22122]\": \"12.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"6.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.92\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"10.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"J. Wook Lim, M. Shin, D. J. Lee, S. Hyun Lee, S. Jin Yun, Sol. Energy Mater. Sol. Cells 2014, 128, 301.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"24.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.3\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"M. Saifullah, S. Ahn, J. Gwak, S. Ahn, K. Kim, J. Cho, J. H. Park, Y. J. Eo, A. Cho, J.-S. Yoo, J. H. Yun, J. Mater. Chem. A 2016, 4, 10542.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"26.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.4\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"A. Mutalikdesai, S. K. Ramasesha, Thin Solid Films 2017, 632, 73.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"43.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CdTe\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"27.2\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"101.0\"}, {\"Refs.\": \"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"21.8\", \"200 h PCE [%]\": \"22.0\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"21.8\", \"AVT [%]\": \"\", \"Absorber\": \"Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, N2, 40\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.2\", \"E1000h [Wh cm\\u22122]\": \"22.0\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"D. Bi, X. Li, J. V. Mili\\u0107, D. J. Kubicki, N. Pellet, J. Luo, T. LaGrange, P. Mettraux, L. Emsley, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Nat. Commun. 2018, 9, 4482.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"20.6\", \"200 h PCE [%]\": \"20.2\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"20.2\", \"AVT [%]\": \"\", \"Absorber\": \"FAxCs1\\u2212xPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, w-LED, Ar, 55 60\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.1\", \"E1000h [Wh cm\\u22122]\": \"20.1\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"S. Bai, P. Da, C. Li, Z. Wang, Z. Yuan, F. Fu, M. Kawecki, X. Liu, N. Sakai, J. T.-W. Wang, S. Huettner, S. Buecheler, M. Fahlman, F. Gao, H. J. Snaith, Nature 2019, 571, 245.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"19.2\", \"200 h PCE [%]\": \"19.3\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"18.4\", \"AVT [%]\": \"\", \"Absorber\": \"(FA0.83MA0.17)0.95Cs0.05Pb(I0.9Br0.1)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, encapsulation, 70 75\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"3.9\", \"E1000h [Wh cm\\u22122]\": \"19.0\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"A. D. Jodlowski, C. Rold\\u00e1n-Carmona, G. Grancini, M. Salado, M. Ralaiarisoa, S. Ahmad, N. Koch, L. Camacho, G. de Miguel, M. K. Nazeeruddin, Nat. Energy 2017, 2, 972.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"17.1\", \"200 h PCE [%]\": \"11.6\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"9.5\", \"AVT [%]\": \"\", \"Absorber\": \"MA0.85Gua0.15PbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, Ar, 60\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"2.8\", \"E1000h [Wh cm\\u22122]\": \"11.1\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"L. Wang, H. Zhou, J. Hu, B. Huang, M. Sun, B. Dong, G. Zheng, Y. Huang, Y. Chen, L. Li, Z. Xu, N. Li, Z. Liu, Q. Chen, L.-D. Sun, C.-H. Yan, Science 2019, 363, 265.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"19.2\", \"200 h PCE [%]\": \"19.5\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"17.6\", \"AVT [%]\": \"\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.1\", \"E1000h [Wh cm\\u22122]\": \"19.1\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"S. Yang, S. Chen, E. Mosconi, Y. Fang, X. Xiao, C. Wang, Y. Zhou, Z. Yu, J. Zhao, Y. Gao, F. De Angelis, J. Huang, Science 2019, 365, 473.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"19.6\", \"200 h PCE [%]\": \"19.6\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"18.8\", \"AVT [%]\": \"\", \"Absorber\": \"Cs0.05FA0.81MA0.14PbI2.55Br0.45\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP-RL, AM1.5G, encapsulation, 50 70% RH, 65\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"3.9\", \"E1000h [Wh cm\\u22122]\": \"19.4\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"A. D. Jodlowski, C. Rold\\u00e1n-Carmona, G. Grancini, M. Salado, M. Ralaiarisoa, S. Ahmad, N. Koch, L. Camacho, G. de Miguel, M. K. Nazeeruddin, Nat. Energy 2017, 2, 972.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"18.1\", \"200 h PCE [%]\": \"11.9\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"13.6\", \"AVT [%]\": \"\", \"Absorber\": \"MA0.75Gua0.25PbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, Ar, 60\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"2.6\", \"E1000h [Wh cm\\u22122]\": \"13.0\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"J. A. Christians, P. Schulz, J. S. Tinkham, T. H. Schloemer, S. P. Harvey, B. J. Tremolet de Villers, A. Sellinger, J. J. Berry, J. M. Luther, Nat. Energy 2018, 3, 68.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"12.2\", \"200 h PCE [%]\": \"13.3\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"12.3\", \"AVT [%]\": \"\", \"Absorber\": \"(FA0.79MA0.16Cs0.05)0.97Pb(I0.84Br0.16)2.97\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"77 mW cm\\u22122, MPP-RL, AM1.5G, RH<25%, 26\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"2.1\", \"E1000h [Wh cm\\u22122]\": \"9.9\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"M. Saliba, T. Matsui, J.-Y. Seo, K. Domanski, J.-P. Correa-Baena, M. K. Nazeeruddin, S. M. Zakeeruddin, W. Tress, A. Abate, A. Hagfeldt, M. Gr\\u00e4tzel, Energy Environ. Sci. 2016, 9, 1989.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"20.1\", \"200 h PCE [%]\": \"17.8\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"Cs0.1(MA0.17FA0.83)0.9Pb(I0.83Br0.17)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, w-LED, N2, 25\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"3.7\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"K. Domanski, E. A. Alharbi, A. Hagfeldt, M. Gr\\u00e4tzel, W. Tress, Nat. Energy 2018, 3, 61.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"19.7\", \"200 h PCE [%]\": \"17.2\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"Cs0.5(FA0.83MA0.17)0.95Pb(I0.83Br0.17)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, w-LED, N2, 20\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"3.5\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"K. A. Bush, A. F. Palmstrom, Z. J. Yu, M. Boccard, R. Cheacharoen, J. P. Mailoa, D. P. McMeekin, R. L. Z. Hoye, C. D. Bailie, T. Leijtens, I. M. Peters, M. C. Minichetti, N. Rolston, R. Prasanna, S. Sofia, D. Harwood, W. Ma, F. Moghadam, H. J. Snaith, T. Buonassisi, Z. C. Holman, S. F. Bent, M. D. McGehee, Nat. Energy 2017, 2, 17009.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"13.0\", \"200 h PCE [%]\": \"14.7\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"13.0\", \"AVT [%]\": \"\", \"Absorber\": \"Cs0.17FA0.83Pb(Br0.17I0.83)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, 40% RH, 35\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"2.8\", \"E1000h [Wh cm\\u22122]\": \"14.1\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"M. Chen, M.-G. Ju, H. F. Garces, A. D. Carl, L. K. Ono, Z. Hawash, Y. Zhang, T. Shen, Y. Qi, R. L. Grimm, D. Pacifici, X. C. Zeng, Y. Zhou, N. P. Padture, Nat. Commun. 2019, 10, 16.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"6.8\", \"200 h PCE [%]\": \"6.7\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"CsSn0.5Ge0.5I3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP , AM1.5G, N2, 45\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.3\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"P. Wang, X. Zhang, Y. Zhou, Q. Jiang, Q. Ye, Z. Chu, X. Li, X. Yang, Z. Yin, J. You, Nat. Commun. 2018, 9, 2225.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"12.9\", \"200 h PCE [%]\": \"13.4\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"CsPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, N2, 25\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"2.7\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"7.8\", \"200 h PCE [%]\": \"7.2\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"6.8\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:ITIC-2F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, N2, 40\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.5\", \"E1000h [Wh cm\\u22122]\": \"7.0\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"C. Xie, T. Heum\\u00fcller, W. Gruber, X. Tang, A. Classen, I. Schuldes, M. Bidwell, A. Sp\\u00e4th, R. H. Fink, T. Unruh, I. McCulloch, N. Li, C. J. Brabec, Nat. Commun. 2018, 9, 5335.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"5.0\", \"200 h PCE [%]\": \"5.0\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"4.7\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"P3HT:o-IDTBR\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, N2, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.0\", \"E1000h [Wh cm\\u22122]\": \"4.8\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.0\", \"200 h PCE [%]\": \"7.4\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"7.0\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:ITIC-Th\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, N2, 40\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.5\", \"E1000h [Wh cm\\u22122]\": \"7.3\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"A. Classen, T. Heumueller, I. Wabra, J. Gerner, Y. He, L. Einsiedler, N. Li, G. J. Matt, A. Osvet, X. Du, A. Hirsch, C. J. Brabec, Adv. Energy Mater. 2019, 9, 1902124.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.7\", \"200 h PCE [%]\": \"8.1\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:IDTBR\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, N2, 35 40\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.6\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"5.9\", \"200 h PCE [%]\": \"5.6\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"5.4\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:PCBM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, N2, 40\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.1\", \"E1000h [Wh cm\\u22122]\": \"5.6\", \"Eg [eV]\": \"1.84\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"M. Ra\\u00efssi, S. Leroy-Lhez, B. Ratier, Org. Electron. 2016, 37, 183.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"3.7\", \"200 h PCE [%]\": \"3.7\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"3.7\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"P3HT-PCBM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, air\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"0.7\", \"E1000h [Wh cm\\u22122]\": \"3.7\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"9.0\", \"200 h PCE [%]\": \"9.0\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"8.2\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 65\\u00a0\\u00b0C\", \"Dye sensitizer\": \"TF-tBu_C3F7\", \"E200h [Wh cm\\u22122]\": \"1.8\", \"E1000h [Wh cm\\u22122]\": \"8.7\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"S. G. Hashmi, M. \\u00d6zkan, J. Halme, S. M. Zakeeruddin, J. Paltakari, M. Gr\\u00e4tzel, P. D. Lund, Energy Environ. Sci. 2016, 9, 2453.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"6.5\", \"200 h PCE [%]\": \"6.7\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"6.3\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 35\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"1.4\", \"E1000h [Wh cm\\u22122]\": \"6.6\", \"Eg [eV]\": \"1.75\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"R. Jiang, A. Anderson, P. R. F. Barnes, L. Xiaoe, C. Law, B. C. O'Regan, J. Mater. Chem. A 2014, 2, 4751.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"6.3\", \"200 h PCE [%]\": \"5.8\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"4.8\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, 20\\u00a0\\u00b0C\", \"Dye sensitizer\": \"Z907\", \"E200h [Wh cm\\u22122]\": \"1.3\", \"E1000h [Wh cm\\u22122]\": \"5.5\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"S. M. Seo, C. K. Kim, H. K. Kim, J. Mater. Chem. A 2019, 7, 14743.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"9.3\", \"200 h PCE [%]\": \"9.9\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"7.9\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 50\\u00a0\\u00b0C\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"1.9\", \"E1000h [Wh cm\\u22122]\": \"9.2\", \"Eg [eV]\": \"1.78\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.4\", \"200 h PCE [%]\": \"8.3\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED\", \"Dye sensitizer\": \"MK2\", \"E200h [Wh cm\\u22122]\": \"1.7\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"J. Xia, Q. Wang, M. Chen, W. Li, J. Liu, J. Chen, H. Wu, S. Fan, Electrochim. Acta 2019, 307, 422.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.0\", \"200 h PCE [%]\": \"8.3\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"8.3\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G\", \"Dye sensitizer\": \"N719\", \"E200h [Wh cm\\u22122]\": \"1.4\", \"E1000h [Wh cm\\u22122]\": \"8.1\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"J. Gao, M. Bhagavathi Achari, L. Kloo, Chem. Commun. 2014, 50, 6249.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"5.8\", \"200 h PCE [%]\": \"6.5\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"5.9\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 60\\u00a0\\u00b0C\", \"Dye sensitizer\": \"D35\", \"E200h [Wh cm\\u22122]\": \"1.3\", \"E1000h [Wh cm\\u22122]\": \"6.2\", \"Eg [eV]\": \"2.07\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver1_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"T. Jiang, Z. Chen, X. Chen, T. Liu, X. Chen, W. E. I. Sha, H. Zhu, Y. Yang, Sol. RRL 2020, 4, 1900467.\", \"PCE [%]\": \"20.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FASnI3)0.6(MAPbI3)0.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.25\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"30.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"843.0\"}, {\"Refs.\": \"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"GuaSCN:(FASnI3)0.6(MAPbI3)0.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.26\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"30.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"834.0\"}, {\"Refs.\": \"C. Li, Z. Song, D. Zhao, C. Xiao, B. Subedi, N. Shrestha, M. M. Junda, C. Wang, C.-S. Jiang, M. Al-Jassim, R. J. Ellingson, N. J. Podraza, K. Zhu, Y. Yan, Adv. Energy Mater. 2019, 9, 1803135.\", \"PCE [%]\": \"19.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FASnI3)0.6(MAPbI3)0.34(MAPbBr3)0.06\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.26\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.5\", \"Jsc [mA cm\\u22122]\": \"28.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"888.0\"}, {\"Refs.\": \"R. Lin, K. Xiao, Z. Qin, Q. Han, C. Zhang, M. Wei, M. I. Saidaminov, Y. Gao, J. Xu, M. Xiao, A. Li, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2019, 4, 864.\", \"PCE [%]\": \"20.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA0.3FA0.7Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.27\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.5\", \"Jsc [mA cm\\u22122]\": \"31.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"827.0\"}, {\"Refs.\": \"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\", \"PCE [%]\": \"20.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FSA:MA0.3FA0.7Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.1\", \"Jsc [mA cm\\u22122]\": \"30.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"842.0\"}, {\"Refs.\": \"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\", \"PCE [%]\": \"21.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FSA:MA0.3FA0.7Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.8\", \"Jsc [mA cm\\u22122]\": \"31.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.5MA0.45Cs0.05Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"30.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"G. Kapil, T. Bessho, C. H. Ng, K. Hamada, M. Pandey, M. A. Kamarudin, D. Hirotani, T. Kinoshita, T. Minemoto, Q. Shen, T. Toyoda, T. N. Murakami, H. Segawa, S. Hayase, ACS Energy Lett. 2019, 4, 1991.\", \"PCE [%]\": \"18.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.025FA0.475MA0.5Sn0.5Pb0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"32.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"S. Shao, Y. Cui, H. Duim, X. Qiu, J. Dong, G. H. ten Brink, G. Portale, R. C. Chiechi, S. Zhang, J. Hou, M. A. Loi, Adv. Mater. 2018, 30, 1803703.\", \"PCE [%]\": \"16.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASn0.5Pb0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.29\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"29.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"771.0\"}, {\"Refs.\": \"T. S. Ripolles, D. Yamasuso, Y. Zhang, M. A. Kamarudin, C. Ding, D. Hirotani, Q. Shen, S. Hayase, J. Phys. Chem. C 2018, 122, 27284.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FASnI3)0.6(MAPbI3)0.3(MAPbBr3)0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.29\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"26.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"H. Chen, Z. Peng, K. Xu, Q. Wei, D. Yu, C. Han, H. Li, Z. Ning, Sci. China Mater. 2021, 64, 537.\", \"PCE [%]\": \"18.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FASnI3)0.6(MAPbI3)0.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"29.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"N. Ghimire, R. S. Bobba, A. Gurung, K. M. Reza, M. A. R. Laskar, B. S. Lamsal, K. Emshadi, R. Pathak, M. A. Afroz, A. H. Chowdhury, K. Chen, B. Bahrami, S. I. Rahman, J. Pokharel, A. Baniya, M. T. Rahman, Y. Zhou, Q. Qiao, ACS Appl. Energy Mater. 2021, 4, 1731.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.8MA0.15Cs0.05Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"27.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"Y. Wang, J. Tu, T. Li, C. Tao, X. Deng, Z. Li, J. Mater. Chem. A 2019, 7, 7683.\", \"PCE [%]\": \"5.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsSnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"50.3\", \"Jsc [mA cm\\u22122]\": \"23.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"420.0\"}, {\"Refs.\": \"F. Li, C. Zhang, J.-H. Huang, H. Fan, H. Wang, P. Wang, C. Zhan, C.-M. Liu, X. Li, L.-M. Yang, Y. Song, K.-J. Jiang, Angew. Chem., Int. Ed. 2019, 58, 6688.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.0\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"486.0\"}, {\"Refs.\": \"G. E. Eperon, T. Leijtens, K. A. Bush, R. Prasanna, T. Green, J. T.-W. Wang, D. P. McMeekin, G. Volonakis, R. L. Milot, R. May, A. Palmstrom, D. J. Slotcavage, R. A. Belisle, J. B. Patel, E. S. Parrott, R. J. Sutton, W. Ma, F. Moghadam, B. Conings, A. Babayigit, H.-G. Boyen, S. Bent, F. Giustino, L. M. Herz, M. B. Johnston, M. D. McGehee, H. J. Snaith, Science 2016, 354, 861.\", \"PCE [%]\": \"14.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.75Cs0.25Sn0.5Pb0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.4\", \"Jsc [mA cm\\u22122]\": \"26.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"740.0\"}, {\"Refs.\": \"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.4Sn0.6I2.8Br0.2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.9\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"T. Ye, K. Wang, Y. Hou, D. Yang, N. Smith, B. Magill, J. Yoon, R. R. H. H. Mudiyanselage, G. A. Khodaparast, K. Wang, S. Priya, J. Am. Chem. Soc. 2021, 143, 4319.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsSnI3:MBAA\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"133.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.0\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"450.0\"}, {\"Refs.\": \"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. G\\u00f6del, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.4Sn0.6I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.6\", \"Jsc [mA cm\\u22122]\": \"20.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"767.0\"}, {\"Refs.\": \"S. Lee, D.-W. Kang, ACS Appl. Mater. Interfaces 2017, 9, 22432.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.4Sn0.6I2.6Br0.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.1\", \"Jsc [mA cm\\u22122]\": \"20.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"X. Lian, J. Chen, Y. Zhang, M. Qin, J. Li, S. Tian, W. Yang, X. Lu, G. Wu, H. Chen, Adv. Funct. Mater. 2019, 29, 1807024.\", \"PCE [%]\": \"16.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPb0.7Sn0.3I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"26.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"B. Li, H. Di, B. Chang, R. Yin, L. Fu, Y.-N. Zhang, L. Yin, Adv. Funct. Mater. 2021, 31, 2007447.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsSnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.36\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.1\", \"Jsc [mA cm\\u22122]\": \"19.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"M. Zhang, D. Chi, J. Wang, F. Wu, S. Huang, Sol. Energy 2020, 201, 589.\", \"PCE [%]\": \"14.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.3MA0.7Pb0.7Sn0.3I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.6\", \"Jsc [mA cm\\u22122]\": \"27.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"737.0\"}, {\"Refs.\": \"D. Chi, S. Huang, M. Zhang, S. Mu, Y. Zhao, Y. Chen, J. You, Adv. Funct. Mater. 2018, 28, 1804603.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPb0.75Sn0.25I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.4\", \"Jsc [mA cm\\u22122]\": \"28.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"H. L. Zhu, J. Xiao, J. Mao, H. Zhang, Y. Zhao, W. C. H. Choy, Adv. Funct. Mater. 2017, 27, 1605469.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.75Sn0.25I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.5\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"800.0\"}, {\"Refs.\": \"X. Zhou, L. Zhang, X. Wang, C. Liu, S. Chen, M. Zhang, X. Li, W. Yi, B. Xu, Adv. Mater. 2020, 32, 1908107.\", \"PCE [%]\": \"20.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.7MA0.3Pb0.7Sn0.3I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.0\", \"Jsc [mA cm\\u22122]\": \"26.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"B. Zhao, M. Abdi-Jalebi, M. Tabachnyk, H. Glass, V. S. Kamboj, W. Nie, A. J. Pearson, Y. Puttisong, K. C. G\\u00f6del, H. E. Beere, D. A. Ritchie, A. D. Mohite, S. E. Dutton, R. H. Friend, A. Sadhanala, Adv. Mater. 2017, 29, 1604744.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.6Sn0.4I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.8\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"745.0\"}, {\"Refs.\": \"P. Wang, F. Li, K.-J. Jiang, Y. Zhang, H. Fan, Y. Zhang, Y. Miao, J.-H. Huang, C. Gao, X. Zhou, F. Wang, L.-M. Yang, C. Zhan, Y. Song, Adv. Sci. 2020, 7, 1903047.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.2\", \"Jsc [mA cm\\u22122]\": \"20.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"570.0\"}, {\"Refs.\": \"D. B. Khadka, Y. Shirai, M. Yanagida, K. Miyano, J. Mater. Chem. C 2020, 8, 2307.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA1\\u2212xRbxSnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.6\", \"Jsc [mA cm\\u22122]\": \"20.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"487.0\"}, {\"Refs.\": \"Z. Yang, A. Rajagopal, C.-C. Chueh, S. B. Jo, B. Liu, T. Zhao, A. K. Y. Jen, Adv. Mater. 2016, 28, 8990.\", \"PCE [%]\": \"14.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.75Sn0.25I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"22.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"K. Nishimura, M. A. Kamarudin, D. Hirotani, K. Hamada, Q. Shen, S. Iikubo, T. Minemoto, K. Yoshino, S. Hayase, Nano Energy 2020, 74, 104858.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.9EA0.1)0.98EDA0.01SnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"X. Jiang, F. Wang, Q. Wei, H. Li, Y. Shang, W. Zhou, C. Wang, P. Cheng, Q. Chen, L. Chen, Z. Ning, Nat. Commun. 2020, 11, 1245.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"PEA0.15FA0.85SnI3:NH4SCN\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.9\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"949.0\"}, {\"Refs.\": \"X. Liu, Y. Wang, T. Wu, X. He, X. Meng, J. Barbaud, H. Chen, H. Segawa, X. Yang, L. Han, Nat. Commun. 2020, 11, 2678.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8SnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.2\", \"Jsc [mA cm\\u22122]\": \"21.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"X. Liu, Y. Wang, T. Wu, X. He, X. Meng, J. Barbaud, H. Chen, H. Segawa, X. Yang, L. Han, Nat. Commun. 2020, 11, 2678.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8SnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"22.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"642.0\"}, {\"Refs.\": \"X. Meng, Y. Wang, J. Lin, X. Liu, X. He, J. Barbaud, T. Wu, T. Noda, X. Yang, L. Han, Joule 2020, 4, 902.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASnI3:FOEI\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.5\", \"Jsc [mA cm\\u22122]\": \"22.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"638.0\"}, {\"Refs.\": \"S. Ma, X. Gu, A. K. Kyaw, D. H. Wang, S. Priya, T. Ye, ACS Appl. Mater. Interfaces 2021, 13, 1345.\", \"PCE [%]\": \"6.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsSnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.48\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"53.9\", \"Jsc [mA cm\\u22122]\": \"23.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"460.0\"}, {\"Refs.\": \"A. Y. Alsalloum, B. Turedi, K. Almasabi, X. Zheng, R. Naphade, S. D. Stranks, O. F. Mohammed, O. M. Bakr, Energy Environ. Sci. 2021, 14, 2263.\", \"PCE [%]\": \"22.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.6MA0.4PbI3 (sc)\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.49\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"26.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"Y. Zhao, X. Xu, H. Zhang, J. Shi, L. Zhu, H. Wu, D. Li, Y. Luo, Q. Meng, J. Power Sources 2017, 359, 147.\", \"PCE [%]\": \"19.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.6MA0.4PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.51\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"23.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1047.0\"}, {\"Refs.\": \"S. Yuan, Y. Cai, S. Yang, H. Zhao, F. Qian, Y. Han, J. Sun, Z. Liu, S. Liu, Sol. RRL 2019, 3, 1900220.\", \"PCE [%]\": \"22.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.85MA0.15PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.6\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"J. Jeong, M. Kim, J. Seo, H. Lu, P. Ahlawat, A. Mishra, Y. Yang, M. A. Hope, F. T. Eickemeyer, M. Kim, Y. J. Yoon, I. W. Choi, B. P. Darwich, S. J. Choi, Y. Jo, J. H. Lee, B. Walker, S. M. Zakeeruddin, L. Emsley, U. Rothlisberger, A. Hagfeldt, D. S. Kim, M. Gr\\u00e4tzel, J. Y. Kim, Nature 2021, 592, 381.\", \"PCE [%]\": \"25.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\\u03b1-FAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.8\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1174.0\"}, {\"Refs.\": \"J. Jeong, M. Kim, J. Seo, H. Lu, P. Ahlawat, A. Mishra, Y. Yang, M. A. Hope, F. T. Eickemeyer, M. Kim, Y. J. Yoon, I. W. Choi, B. P. Darwich, S. J. Choi, Y. Jo, J. H. Lee, B. Walker, S. M. Zakeeruddin, L. Emsley, U. Rothlisberger, A. Hagfeldt, D. S. Kim, M. Gr\\u00e4tzel, J. Y. Kim, Nature 2021, 592, 381.\", \"PCE [%]\": \"24.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\\u03b1-FAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"26.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1185.0\"}, {\"Refs.\": \"P. Wang, B. Chen, R. Li, S. Wang, N. Ren, Y. Li, S. Mazumdar, B. Shi, Y. Zhao, X. Zhang, ACS Energy Lett. 2021, 6, 2121.\", \"PCE [%]\": \"23.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.78MA0.22Pb(IBrCl)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.3\", \"Jsc [mA cm\\u22122]\": \"24.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1200.0\"}, {\"Refs.\": \"M. Green, E. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 3.\", \"PCE [%]\": \"25.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \" \", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.2\", \"Jsc [mA cm\\u22122]\": \"25.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1189.0\"}, {\"Refs.\": \"A. Y. Alsalloum, B. Turedi, X. Zheng, S. Mitra, A. A. Zhumekenov, K. J. Lee, P. Maity, I. Gereige, A. AlSaggaf, I. S. Roqan, O. F. Mohammed, O. M. Bakr, ACS Energy Lett. 2020, 5, 657.\", \"PCE [%]\": \"20.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3 (sc)\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"23.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1143.0\"}, {\"Refs.\": \"M. Jeong, I. W. Choi, E. M. Go, Y. Cho, M. Kim, B. Lee, S. Jeong, Y. Jo, H. W. Choi, J. Lee, J.-H. Bae, S. K. Kwak, D. S. Kim, C. Yang, Science 2020, 369, 1615.\", \"PCE [%]\": \"24.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.6\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1181.0\"}, {\"Refs.\": \"W. S. Yang, B.-W. Park, E. H. Jung, N. J. Jeon, Y. C. Kim, D. U. Lee, S. S. Shin, J. Seo, E. K. Kim, J. H. Noh, S. I. Seok, Science 2017, 356, 1376.\", \"PCE [%]\": \"22.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.9(MAPbBr3)0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.3\", \"Jsc [mA cm\\u22122]\": \"25.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1105.0\"}, {\"Refs.\": \"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\", \"PCE [%]\": \"21.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.70MA0.25PbI3-DAP\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1160.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\", \"PCE [%]\": \"25.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \" \", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.8\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1180.0\"}, {\"Refs.\": \"J. J. Yoo, G. Seo, M. R. Chua, T. G. Park, Y. Lu, F. Rotermund, Y.-K. Kim, C. S. Moon, N. J. Jeon, J.-P. Correa-Baena, V. Bulovi\\u0107, S. S. Shin, M. G. Bawendi, J. Seo, Nature 2021, 590, 587.\", \"PCE [%]\": \"25.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAMAPb(IBrCl)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.8\", \"Jsc [mA cm\\u22122]\": \"25.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1181.0\"}, {\"Refs.\": \"J. J. Yoo, G. Seo, M. R. Chua, T. G. Park, Y. Lu, F. Rotermund, Y.-K. Kim, C. S. Moon, N. J. Jeon, J.-P. Correa-Baena, V. Bulovi\\u0107, S. S. Shin, M. G. Bawendi, J. Seo, Nature 2021, 590, 587.\", \"PCE [%]\": \"25.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAMAPb(IBrCl)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.6\", \"Jsc [mA cm\\u22122]\": \"25.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1193.0\"}, {\"Refs.\": \"G. Xu, R. Xue, S. J. Stuard, H. Ade, C. Zhang, J. Yao, Y. Li, Y. Li, Adv. Mater. 2021, 33, 2006753.\", \"PCE [%]\": \"21.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Rb0.05Cs0.05FA0.8MA0.1PbI2.85Br0.15\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.4\", \"Jsc [mA cm\\u22122]\": \"24.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\", \"PCE [%]\": \"23.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.6\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"X. Zheng, Y. Hou, C. Bao, J. Yin, F. Yuan, Z. Huang, K. Song, J. Liu, J. Troughton, N. Gasparini, C. Zhou, Y. Lin, D.-J. Xue, B. Chen, A. K. Johnston, N. Wei, M. N. Hedhili, M. Wei, A. Y. Alsalloum, P. Maity, B. Turedi, C. Yang, D. Baran, T. D. Anthopoulos, Y. Han, Z.-H. Lu, O. F. Mohammed, F. Gao, E. H. Sargent, O. M. Bakr, Nat. Energy 2020, 5, 131.\", \"PCE [%]\": \"22.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(FA0.92MA0.08)0.95Pb(I0.92Br0.08)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.0\", \"Jsc [mA cm\\u22122]\": \"23.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1143.0\"}, {\"Refs.\": \"S. Gharibzadeh, P. Fassl, I. Hossain, P. N. Rohrbeck, M. Frericks, M. Schmidt, T. Duong, M. R. Khan, T. Abzieher, B. Abdollahi Nejand, F. Schackmar, O. Almora, T. Feeney, R. Singh, D. Fuchs, U. Lemmer, J. P. Hofmann, S. Weber, U. W. Paetzold, Energy Environ. Sci. 2021, https://doi.org/10.1039/D1EE01508G.\", \"PCE [%]\": \"22.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.18FA0.82PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.2\", \"Jsc [mA cm\\u22122]\": \"23.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1162.0\"}, {\"Refs.\": \"J. J. Yoo, S. Wieghold, M. C. Sponseller, M. R. Chua, S. N. Bertram, N. T. P. Hartono, J. S. Tresback, E. C. Hansen, J.-P. Correa-Baena, V. Bulovi\\u0107, T. Buonassisi, S. S. Shin, M. G. Bawendi, Energy Environ. Sci. 2019, 12, 2192.\", \"PCE [%]\": \"22.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.92(MAPbBr3)0.08\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.6\", \"Jsc [mA cm\\u22122]\": \"24.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1186.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics Res. Appl. 2021, 29, 657.\", \"PCE [%]\": \"22.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \" \", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.4\", \"Jsc [mA cm\\u22122]\": \"22.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1178.0\"}, {\"Refs.\": \"H. B. Lee, N. Kumar, M. M. Ovhal, Y. J. Kim, Y. M. Song, J.-W. Kang, Adv. Funct. Mater. 2020, n/a, 2001559.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(FAPbI3)0.85(MAPbBr3)0.15\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.8\", \"Jsc [mA cm\\u22122]\": \"23.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1125.0\"}, {\"Refs.\": \"P. Cui, D. Wei, J. Ji, H. Huang, E. Jia, S. Dou, T. Wang, W. Wang, M. Li, Nat. Energy 2019, 4, 150.\", \"PCE [%]\": \"21.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.15MA0.85PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.6\", \"Jsc [mA cm\\u22122]\": \"24.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"M. Li, Z.-K. Wang, M.-P. Zhuo, Y. Hu, K.-H. Hu, Q.-Q. Ye, S. M. Jain, Y.-G. Yang, X.-Y. Gao, L.-S. Liao, Adv. Mater. 2018, 30, 1800258.\", \"PCE [%]\": \"21.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.9Sn0.05Cu0.05I2.9Br0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.0\", \"Jsc [mA cm\\u22122]\": \"24.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1086.0\"}, {\"Refs.\": \"X. Zheng, B. Chen, J. Dai, Y. Fang, Y. Bai, Y. Lin, H. Wei, Xiao C. Zeng, J. Huang, Nat. Energy 2017, 2, 17102.\", \"PCE [%]\": \"21.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.85MA0.15Pb(I0.85Br0.15)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.7\", \"Jsc [mA cm\\u22122]\": \"23.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"Q. Cao, Y. Li, H. Zhang, J. Yang, J. Han, T. Xu, S. Wang, Z. Wang, B. Gao, J. Zhao, X. Li, X. Ma, M. Zakeeruddin Shaik, E. I. Sha Wei, X. Li, M. Gr\\u00e4tzel, Sci. Adv.7, eabg0633.\", \"PCE [%]\": \"21.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsMAFAPbI3:PPP\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.7\", \"Jsc [mA cm\\u22122]\": \"23.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1131.0\"}, {\"Refs.\": \"L. Wang, H. Zhou, J. Hu, B. Huang, M. Sun, B. Dong, G. Zheng, Y. Huang, Y. Chen, L. Li, Z. Xu, N. Li, Z. Liu, Q. Chen, L.-D. Sun, C.-H. Yan, Science 2019, 363, 265.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\\u2212xClx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.4\", \"Jsc [mA cm\\u22122]\": \"23.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1130.0\"}, {\"Refs.\": \"S. Xiong, Z. Hou, S. Zou, X. Lu, J. Yang, T. Hao, Z. Zhou, J. Xu, Y. Zeng, W. Xiao, W. Dong, D. Li, X. Wang, Z. Hu, L. Sun, Y. Wu, X. Liu, L. Ding, Z. Sun, M. Fahlman, Q. Bao, Joule 2021, 5, 467.\", \"PCE [%]\": \"21.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.9\", \"Jsc [mA cm\\u22122]\": \"23.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"J. Peng, D. Walter, Y. Ren, M. Tebyetekerwa, Y. Wu, T. Duong, Q. Lin, J. Li, T. Lu, A. Mahmud Md, C. Lem Olivier Lee, S. Zhao, W. Liu, Y. Liu, H. Shen, L. Li, F. Kremer, T. Nguyen Hieu, D.-Y. Choi, J. Weber Klaus, R. Catchpole Kylie, P. White Thomas, Science 2021, 371, 390.\", \"PCE [%]\": \"21.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.88MA0.07PbI2.56Br0.44\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.6\", \"Jsc [mA cm\\u22122]\": \"21.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1192.0\"}, {\"Refs.\": \"J. Peng, D. Walter, Y. Ren, M. Tebyetekerwa, Y. Wu, T. Duong, Q. Lin, J. Li, T. Lu, A. Mahmud Md, C. Lem Olivier Lee, S. Zhao, W. Liu, Y. Liu, H. Shen, L. Li, F. Kremer, T. Nguyen Hieu, D.-Y. Choi, J. Weber Klaus, R. Catchpole Kylie, P. White Thomas, Science 2021, 371, 390.\", \"PCE [%]\": \"23.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.88MA0.07PbI2.56Br0.44\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.5\", \"Jsc [mA cm\\u22122]\": \"22.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1240.0\"}, {\"Refs.\": \"M. A. Mahmud, T. Duong, Y. Yin, H. T. Pham, D. Walter, J. Peng, Y. Wu, L. Li, H. Shen, N. Wu, N. Mozaffari, G. Andersson, K. R. Catchpole, K. J. Weber, T. P. White, Adv. Funct. Mater. 2020, 30, 1907962.\", \"PCE [%]\": \"22.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.07Rb0.03FA0.765MA0.135PbI2.55Br0.45\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.5\", \"Jsc [mA cm\\u22122]\": \"24.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1200.0\"}, {\"Refs.\": \"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\", \"PCE [%]\": \"21.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3-DAP\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.7\", \"Jsc [mA cm\\u22122]\": \"22.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1180.0\"}, {\"Refs.\": \"K. Choi, J. Lee, H. I. Kim, C. W. Park, G.-W. Kim, H. Choi, S. Park, S. A. Park, T. Park, Energy Environ. Sci. 2018, 11, 3238.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.76MA0.19PbBr0.6I2.4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.8\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1130.0\"}, {\"Refs.\": \"X. Zhao, C. Yao, T. Liu, J. C. HamillJr, G. O. Ngongang Ndjawa, G. Cheng, N. Yao, H. Meng, Y.-L. Loo, Adv. Mater. 2019, 31, 1904494.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.8\", \"Jsc [mA cm\\u22122]\": \"23.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"N. J. Jeon, J. H. Noh, Y. C. Kim, W. S. Yang, S. Ryu, S. I. Seok, Nat. Mater. 2014, 13, 897.\", \"PCE [%]\": \"16.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI1\\u2212xBrx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"19.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1109.0\"}, {\"Refs.\": \"J. H. Noh, S. H. Im, J. H. Heo, T. N. Mandal, S. I. Seok, Nano Lett. 2013, 13, 1764.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.87Br0.13)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.4\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"904.0\"}, {\"Refs.\": \"Y. Yang, C. Liu, O. A. Syzgantseva, M. A. Syzgantseva, S. Ma, Y. Ding, M. Cai, X. Liu, S. Dai, M. K. Nazeeruddin, Adv. Energy Mater. 2021, 11, 2002966.\", \"PCE [%]\": \"17.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(PEA)2(MA)3Pb4I13:NH4I0.2Cl0.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.9\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1190.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"20.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05MA0.15FA0.8Pb(I0.75Br0.25)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.7\", \"Jsc [mA cm\\u22122]\": \"21.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1220.0\"}, {\"Refs.\": \"M. Chen, M.-G. Ju, H. F. Garces, A. D. Carl, L. K. Ono, Z. Hawash, Y. Zhang, T. Shen, Y. Qi, R. L. Grimm, D. Pacifici, X. C. Zeng, Y. Zhou, N. P. Padture, Nat. Commun. 2019, 10, 16.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.74Br0.26)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"10.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"936.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"16.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8Pb(I0.75Br0.25)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.5\", \"Jsc [mA cm\\u22122]\": \"20.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"H. Wang, H. Liu, Z. Dong, W. Li, L. Zhu, H. Chen, Nano Energy 2021, 84, 105881.\", \"PCE [%]\": \"14.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.71\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1056.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"18.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.17Cs0.83PbI2.2Br0.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.72\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.9\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1244.0\"}, {\"Refs.\": \"Z. Liu, J. Siekmann, B. Klingebiel, U. Rau, T. Kirchartz, Adv. Energy Mater. 2021, 11, 2003386.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI2.4Br0.6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.72\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"17.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1350.0\"}, {\"Refs.\": \"D. P. McMeekin, G. Sadoughi, W. Rehman, G. E. Eperon, M. Saliba, M. T. H\\u00f6rantner, A. Haghighirad, N. Sakai, L. Korte, B. Rech, M. B. Johnston, L. M. Herz, H. J. Snaith, Science 2016, 351, 151.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.83Cs0.17Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.72\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1200.0\"}, {\"Refs.\": \"T. Duong, H. Pham, T. C. Kho, P. Phang, K. C. Fong, D. Yan, Y. Yin, J. Peng, M. A. Mahmud, S. Gharibzadeh, B. A. Nejand, I. M. Hossain, M. R. Khan, N. Mozaffari, Y. Wu, H. Shen, J. Zheng, H. Mai, W. Liang, C. Samundsett, M. Stocks, K. McIntosh, G. G. Andersson, U. Lemmer, B. S. Richards, U. W. Paetzold, A. Ho-Ballie, Y. Liu, D. Macdonald, A. Blakers, J. Wong-Leung, T. White, K. Weber, K. Catchpole, Adv. Energy Mater. 2020, 10, 1903553.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Rb0.05Cs0.095MA0.1425FA0.7125PbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.3\", \"Jsc [mA cm\\u22122]\": \"18.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1269.0\"}, {\"Refs.\": \"S. Gharibzadeh, B. Abdollahi Nejand, M. Jakoby, T. Abzieher, D. Hauschild, S. Moghadamzadeh, J. A. Schwenzer, P. Brenner, R. Schmager, A. A. Haghighirad, L. Weinhardt, U. Lemmer, B. S. Richards, I. A. Howard, U. W. Paetzold, Adv. Energy Mater. 2019, 9, 1803699.\", \"PCE [%]\": \"19.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.83Cs0.17Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.75\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1310.0\"}, {\"Refs.\": \"Y. Lin, B. Chen, F. Zhao, X. Zheng, Y. Deng, Y. Shao, Y. Fang, Y. Bai, C. Wang, J. Huang, Adv. Mater. 2017, 29, 1700607.\", \"PCE [%]\": \"18.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.83MA0.17)0.95Cs0.05Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.76\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.4\", \"Jsc [mA cm\\u22122]\": \"20.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1210.0\"}, {\"Refs.\": \"Q. Ye, Y. Zhao, S. Mu, F. Ma, F. Gao, Z. Chu, Z. Yin, P. Gao, X. Zhang, J. You, Adv. Mater. 2019, 31, 1905143.\", \"PCE [%]\": \"18.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI3\\u2212xBrx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.5\", \"Jsc [mA cm\\u22122]\": \"18.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1234.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"15.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.17FA0.83Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.78\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.5\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1210.0\"}, {\"Refs.\": \"H. Tan, F. Che, M. Wei, Y. Zhao, M. I. Saidaminov, P. Todorovi\\u0107, D. Broberg, G. Walters, F. Tan, T. Zhuang, B. Sun, Z. Liang, H. Yuan, E. Fron, J. Kim, Z. Yang, O. Voznyy, M. Asta, E. H. Sargent, Nat. Commun. 2018, 9, 3100.\", \"PCE [%]\": \"19.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.12MA0.05FA0.83Pb(I0.6Br0.4)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"19.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1250.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"16.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.17FA0.83PbI1.8Br1.2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.8\", \"Jsc [mA cm\\u22122]\": \"17.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1284.0\"}, {\"Refs.\": \"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\", \"PCE [%]\": \"13.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbBrI2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"14.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1272.0\"}, {\"Refs.\": \"Z. Yang, Z. Yu, H. Wei, X. Xiao, Z. Ni, B. Chen, Y. Deng, S. N. Habisreutinger, X. Chen, K. Wang, J. Zhao, P. N. Rudd, J. J. Berry, M. C. Beard, J. Huang, Nat. Commun. 2019, 10, 4498.\", \"PCE [%]\": \"16.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.6Cs0.4Pb(I0.65Br0.35)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.6\", \"Jsc [mA cm\\u22122]\": \"17.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1220.0\"}, {\"Refs.\": \"Y.-N. Zhang, B. Li, L. Fu, Y. Zou, Q. Li, L.-W. Yin, Sol. Energy Mater. Sol. Cells 2019, 194, 168.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI1.5Br1.5/CsPbI1.5Br1.5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.0\", \"Jsc [mA cm\\u22122]\": \"21.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"M. Chen, M.-G. Ju, A. D. Carl, Y. Zong, R. L. Grimm, J. Gu, X. C. Zeng, Y. Zhou, N. P. Padture, Joule 2018, 2, 558.\", \"PCE [%]\": \"3.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs2TiBr6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.9\", \"Jsc [mA cm\\u22122]\": \"5.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"M.-J. Wu, C.-C. Kuo, L.-S. Jhuang, P.-H. Chen, Y.-F. Lai, F.-C. Chen, Adv. Energy Mater. 2019, 9, 1901863.\", \"PCE [%]\": \"8.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA0.85Cs0.15Pb(I0.65Br0.35)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.4\", \"Jsc [mA cm\\u22122]\": \"11.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"W.-Q. Wu, Z. Yang, P. N. Rudd, Y. Shao, X. Dai, H. Wei, J. Zhao, Y. Fang, Q. Wang, Y. Liu, Y. Deng, X. Xiao, Y. Feng, J. Huang, Sci. Adv. 2019, 5, eaav8925.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8Pb(I0.6Br0.4)3-DAP\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.84\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1260.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"15.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.17FA0.83PbI1.5Br1.5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1296.0\"}, {\"Refs.\": \"J. Zhang, Z. Wang, A. Mishra, M. Yu, M. Shasti, W. Tress, D. J. Kubicki, C. E. Avalos, H. Lu, Y. Liu, B. I. Carlsen, A. Agarwalla, Z. Wang, W. Xiang, L. Emsley, Z. Zhang, M. Gr\\u00e4tzel, W. Guo, A. Hagfeldt, Joule 2020, 4, 222.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb(I0.75Br0.25)3-0.5FAOAc\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.8\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1340.0\"}, {\"Refs.\": \"W. Xiang, Z. Wang, D. J. Kubicki, X. Wang, W. Tress, J. Luo, J. Zhang, A. Hofstetter, L. Zhang, L. Emsley, M. Gr\\u00e4tzel, A. Hagfeldt, Nat. Commun. 2019, 10, 4686.\", \"PCE [%]\": \"14.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb0.8Ba0.2I2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"14.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1280.0\"}, {\"Refs.\": \"W. Xiang, Z. Wang, D. J. Kubicki, W. Tress, J. Luo, D. Prochowicz, S. Akin, L. Emsley, J. Zhou, G. Dietler, M. Gr\\u00e4tzel, A. Hagfeldt, Joule 2019, 3, 205.\", \"PCE [%]\": \"13.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb0.95Eu0.05I2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.8\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1220.0\"}, {\"Refs.\": \"H. Zhao, Z. Xu, Y. Che, Y. Han, S. Yang, C. Duan, J. Cui, S. Dai, Z. Liu, S. Liu, J. Power Sources 2021, 492, 229580.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"15.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1300.0\"}, {\"Refs.\": \"S. Yang, H. Zhao, Y. Han, C. Duan, Z. Liu, S. Liu, Small 2019, 15, 1904387.\", \"PCE [%]\": \"15.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1250.0\"}, {\"Refs.\": \"J. Li, J. Yang, J. Ma, J. Liang, Y. Liu, X. Hu, C. Chen, W. Yang, J. Min, Q. Bao, G. Fang, C. Tao, Chem. Eng. J. 2021, 417, 129247.\", \"PCE [%]\": \"16.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.89\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"15.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1310.0\"}, {\"Refs.\": \"H. Zhao, Y. Han, Z. Xu, C. Duan, S. Yang, S. Yuan, Z. Yang, Z. Liu, S. Liu, Adv. Energy Mater. 2019, 9, 1902279.\", \"PCE [%]\": \"15.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2\\u2212xBr(Ac)x\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.89\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.3\", \"Jsc [mA cm\\u22122]\": \"15.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1300.0\"}, {\"Refs.\": \"S. S. Mali, J. V. Patil, J. A. Steele, S. R. Rondiya, N. Y. Dzade, C. K. Hong, ACS Energy Lett. 2021, 6, 778.\", \"PCE [%]\": \"15.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"InCl3:CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.9\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"16.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1240.0\"}, {\"Refs.\": \"C. Duan, J. Cui, M. Zhang, Y. Han, S. Yang, H. Zhao, H. Bian, J. Yao, K. Zhao, Z. Liu, S. Liu, Adv. Energy Mater. 2020, 10, 2000691.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.9\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.7\", \"Jsc [mA cm\\u22122]\": \"15.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1320.0\"}, {\"Refs.\": \"Y. Zhou, Y.-H. Jia, H.-H. Fang, M. A. Loi, F.-Y. Xie, L. Gong, M.-C. Qin, X.-H. Lu, C.-P. Wong, N. Zhao, Adv. Funct. Mater. 2018, 28, 1803130.\", \"PCE [%]\": \"14.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.17Cs0.83PbI1.2Br1.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.91\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1312.0\"}, {\"Refs.\": \"X. Pu, J. Han, S. Wang, H. Zhou, Q. Cao, J. Yang, Z. He, X. Li, J. Materiomics 2021, 7, 1039.\", \"PCE [%]\": \"14.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI2Br\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.91\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.9\", \"Jsc [mA cm\\u22122]\": \"15.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1160.0\"}, {\"Refs.\": \"K. M. Boopathi, P. Karuppuswamy, A. Singh, C. Hanmandlu, L. Lin, S. A. Abbas, C. C. Chang, P. C. Wang, G. Li, C. W. Chu, J. Mater. Chem. A 2017, 5, 20843.\", \"PCE [%]\": \"2.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA3Sb2I9+HI\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.91\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.8\", \"Jsc [mA cm\\u22122]\": \"5.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"620.0\"}, {\"Refs.\": \"I. Turkevych, S. Kazaoui, E. Ito, T. Urano, K. Yamada, H. Tomiyasu, H. Yamagishi, M. Kondo, S. Aramaki, ChemSusChem 2017, 10, 3754.\", \"PCE [%]\": \"4.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Ag3BiI6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.8\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\", \"PCE [%]\": \"2.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"AgBiI4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.7\", \"Jsc [mA cm\\u22122]\": \"5.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"670.0\"}, {\"Refs.\": \"B. Ghosh, B. Wu, X. Guo, P. C. Harikesh, R. A. John, T. Baikie, Arramel, A. T. S. Wee, C. Guet, T. C. Sum, S. Mhaisalkar, N. Mathews, Adv. Energy Mater. 2018, 8, 1802051.\", \"PCE [%]\": \"2.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"AgBiI5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.95\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.4\", \"Jsc [mA cm\\u22122]\": \"6.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"B.-W. Park, B. Philippe, X. Zhang, H. Rensmo, G. Boschloo, E. M. J. Johansson, Adv. Mater. 2015, 27, 6806.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs3Bi2I9\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.97\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.6\", \"Jsc [mA cm\\u22122]\": \"2.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"J. Liang, P. Zhao, C. Wang, Y. Wang, Y. Hu, G. Zhu, L. Ma, J. Liu, Z. Jin, J. Am. Chem. Soc. 2017, 139, 14009.\", \"PCE [%]\": \"8.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.98\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.0\", \"Jsc [mA cm\\u22122]\": \"12.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"D. Forg\\u00e1cs, L. Gil-Escrig, D. P\\u00e9rez-Del-Rey, C. Momblona, J. Werner, B. Niesen, C. Ballif, M. Sessolo, H. J. Bolink, Adv. Energy Mater. 2017, 7, 1602121.\", \"PCE [%]\": \"9.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.15FA0.85Pb(I0.3Br0.7)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1185.0\"}, {\"Refs.\": \"S. A. Kulkarni, T. Baikie, P. P. Boix, N. Yantara, N. Mathews, S. Mhaisalkar, J. Mater. Chem. A 2014, 2, 9221.\", \"PCE [%]\": \"2.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.41Br0.59)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.03\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.7\", \"Jsc [mA cm\\u22122]\": \"6.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"836.0\"}, {\"Refs.\": \"Q. Xue, G. Chen, M. Liu, J. Xiao, Z. Chen, Z. Hu, X.-F. Jiang, B. Zhang, F. Huang, W. Yang, H.-L. Yip, Y. Cao, Adv. Energy Mater. 2016, 6, 1502021.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb(I0.3Br0.7)xCl3\\u2212x(Br)\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.04\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"9.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1340.0\"}, {\"Refs.\": \"Y. Zhao, A. M. Nardes, K. Zhu, Faraday Discuss. 2014, 176, 301.\", \"PCE [%]\": \"6.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.1\", \"Jsc [mA cm\\u22122]\": \"5.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1450.0\"}, {\"Refs.\": \"H. Wang, S. Cao, B. Yang, H. Li, M. Wang, X. Hu, K. Sun, Z. Zang, Sol. RRL 2020, 4, 1900363.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.4\", \"Jsc [mA cm\\u22122]\": \"11.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1270.0\"}, {\"Refs.\": \"W. Zhu, Z. Zhang, W. Chai, Q. Zhang, D. Chen, Z. Lin, J. Chang, J. Zhang, C. Zhang, Y. Hao, ChemSusChem 2019, 12, 2318.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.1\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"11.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1261.0\"}, {\"Refs.\": \"B. Zhang, W. Bi, Y. Wu, C. Chen, H. Li, Z. Song, Q. Dai, L. Xu, H. Song, ACS Appl. Mater. Interfaces 2019, 11, 33868.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"GAI-DEE-CsPbIBr2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.6\", \"Jsc [mA cm\\u22122]\": \"10.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1200.0\"}, {\"Refs.\": \"R. Nie, A. Mehta, B.-w. Park, H.-W. Kwon, J. Im, S. I. Seok, J. Am. Chem. Soc. 2018, 140, 872.\", \"PCE [%]\": \"3.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MASbSI2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.14\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.4\", \"Jsc [mA cm\\u22122]\": \"8.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\", \"PCE [%]\": \"4.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.85MA0.15Pb(I0.85Br0.15)3) R\\u00a0=\\u00a00.7\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.15\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.8\", \"Jsc [mA cm\\u22122]\": \"6.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1084.0\"}, {\"Refs.\": \"T. Bu, X. Liu, R. Chen, Z. Liu, K. Li, W. Li, Y. Peng, Z. Ku, F. Huang, Y.-B. Cheng, J. Zhong, J. Mater. Chem. A 2018, 6, 6319.\", \"PCE [%]\": \"2.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.85MA0.15Pb(I0.85Br0.15)3) R\\u00a0=\\u00a00.56\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.19\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.5\", \"Jsc [mA cm\\u22122]\": \"3.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1051.0\"}, {\"Refs.\": \"F. Umar, J. Zhang, Z. Jin, I. Muhammad, X. Yang, H. Deng, K. Jahangeer, Q. Hu, H. Song, J. Tang, Adv. Opt. Mater. 2019, 7, 1801368.\", \"PCE [%]\": \"1.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs3Sb2I9\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.2\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"55.9\", \"Jsc [mA cm\\u22122]\": \"3.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"610.0\"}, {\"Refs.\": \"Y. Zhang, Y. Liang, Y. Wang, F. Guo, L. Sun, D. Xu, ACS Energy Lett. 2018, 3, 1808.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.27\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.5\", \"Jsc [mA cm\\u22122]\": \"8.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1552.0\"}, {\"Refs.\": \"J. Duan, Y. Zhao, B. He, Q. Tang, Angew. Chem., Int. Ed. 2018, 57, 3787.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.9\", \"Jsc [mA cm\\u22122]\": \"8.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1458.0\"}, {\"Refs.\": \"X. Hu, X.-F. Jiang, X. Xing, L. Nian, X. Liu, R. Huang, K. Wang, H.-L. Yip, G. Zhou, Sol. RRL 2018, 2, 1800083.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"7.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1653.0\"}, {\"Refs.\": \"M. Wang, J. Duan, J. Du, X. Yang, Y. Duan, T. Zhang, Q. Tang, ACS Appl. Mater. Interfaces 2021, 13, 12091.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.0\", \"Jsc [mA cm\\u22122]\": \"6.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1580.0\"}, {\"Refs.\": \"G. Liao, J. Duan, Y. Zhao, Q. Tang, Sol. Energy 2018, 171, 279=.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.1\", \"Jsc [mA cm\\u22122]\": \"7.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1470.0\"}, {\"Refs.\": \"X. Sun, B. He, J. Zhu, R. Zhu, H. Chen, Y. Duan, Q. Tang, Chem. Eng. J. 2021, 412, 128727.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"7.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1602.0\"}, {\"Refs.\": \"J. Zhu, B. He, Z. Gong, Y. Ding, W. Zhang, X. Li, Z. Zong, H. Chen, Q. Tang, ChemSusChem 2020, 13, 1834.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.8\", \"Jsc [mA cm\\u22122]\": \"7.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1584.0\"}, {\"Refs.\": \"Y. Zhao, J. Duan, Y. Wang, X. Yang, Q. Tang, Nano Energy 2020, 67, 104286.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.5\", \"Jsc [mA cm\\u22122]\": \"7.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1622.0\"}, {\"Refs.\": \"Y. Zhao, J. Duan, H. Yuan, Y. Wang, X. Yang, B. He, Q. Tang, Sol. RRL 2019, 3, 1800284.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsSnBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.4\", \"Jsc [mA cm\\u22122]\": \"7.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1610.0\"}, {\"Refs.\": \"C. H. Ng, T. S. Ripolles, K. Hamada, S. H. Teo, H. N. Lim, J. Bisquert, S. Hayase, Sci. Rep. 2018, 8, 2482.\", \"PCE [%]\": \"4.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr2.9I0.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.36\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.6\", \"Jsc [mA cm\\u22122]\": \"5.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1130.0\"}, {\"Refs.\": \"F. Jiang, D. Yang, Y. Jiang, T. Liu, X. Zhao, Y. Ming, B. Luo, F. Qin, J. Fan, H. Han, L. Zhang, Y. Zhou, J. Am. Chem. Soc. 2018, 140, 1019.\", \"PCE [%]\": \"2.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MA3Sb2ClxI9\\u2212x\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.5\", \"Jsc [mA cm\\u22122]\": \"5.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"X. Wan, Z. Yu, W. Tian, F. Huang, S. Jin, X. Yang, Y.-B. Cheng, A. Hagfeldt, L. Sun, J. Energy Chem. 2020, 46, 8.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.8\", \"Jsc [mA cm\\u22122]\": \"6.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1490.0\"}, {\"Refs.\": \"Y. Zhao, H. Xu, Y. Wang, X. Yang, J. Duan, Q. Tang, J. Power Sources 2019, 440, 227151.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.91Rb0.09PbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"8.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1580.0\"}, {\"Refs.\": \"X. Yang, Y. Chen, P. Liu, H. Xiang, W. Wang, R. Ran, W. Zhou, Z. Shao, Adv. Funct. Mater. 2020, 30, 2001557.\", \"PCE [%]\": \"2.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs2AgBiBr6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"51.2\", \"Jsc [mA cm\\u22122]\": \"5.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"M. Safdari, P. H. Svensson, M. T. Hoang, I. Oh, L. Kloo, J. M. Gardner, J. Mater. Chem. A 2016, 4, 15638.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"BdAPbI4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"43.0\", \"Jsc [mA cm\\u22122]\": \"2.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"870.0\"}, {\"Refs.\": \"G. Murugadoss, R. Thangamuthu, S. M. Senthil Kumar, N. Anandhan, M. Rajesh Kumar, A. Rathishkumar, J. Alloys Compd. 2019, 787, 17.\", \"PCE [%]\": \"2.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb2Br5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.3\", \"Jsc [mA cm\\u22122]\": \"5.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"2.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbBr2.1Cl0.9\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.9\", \"Jsc [mA cm\\u22122]\": \"3.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"B. Wang, N. Li, L. Yang, C. Dall'Agnese, A. K. Jena, S.-i. Sasaki, T. Miyasaka, H. Tamiaki, X.-F. Wang, J. Am. Chem. Soc. 2021, 143, 2207.\", \"PCE [%]\": \"2.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs2AgBiBr6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.9\", \"Jsc [mA cm\\u22122]\": \"4.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1010.0\"}, {\"Refs.\": \"E. Greul, Michiel L. Petrus, A. Binek, P. Docampo, T. Bein, J. Mater. Chem. A 2017, 5, 19972.\", \"PCE [%]\": \"1.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs2AgBiBr6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"40.2\", \"Jsc [mA cm\\u22122]\": \"3.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"1.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbBr2Cl\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.48\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.0\", \"Jsc [mA cm\\u22122]\": \"2.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.2\", \"Jsc [mA cm\\u22122]\": \"24.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"X. Song, N. Gasparini, L. Ye, H. Yao, J. Hou, H. Ade, D. Baran, ACS Energy Lett. 2018, 3, 669.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.9\", \"Jsc [mA cm\\u22122]\": \"27.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"712.0\"}, {\"Refs.\": \"X. Song, N. Gasparini, M. M. Nahid, S. H. K. Paleti, C. Li, W. Li, H. Ade, D. Baran, Adv. Funct. Mater. 2019, 29, 1902441.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDTT-DPP:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.2\", \"Jsc [mA cm\\u22122]\": \"19.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"695.0\"}, {\"Refs.\": \"F. Qi, K. Jiang, F. Lin, Z. Wu, H. Zhang, W. Gao, Y. Li, Z. Cai, H. Y. Woo, Z. Zhu, A. K. Y. Jen, ACS Energy Lett. 2021, 6, 9.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:mBzS-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.4\", \"Jsc [mA cm\\u22122]\": \"27.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"804.0\"}, {\"Refs.\": \"S. M. Hosseini, N. Tokmoldin, Y. W. Lee, Y. Zou, H. Y. Woo, D. Neher, S. Shoaee, Sol. RRL 2020, 4, 2000498.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.4\", \"Jsc [mA cm\\u22122]\": \"26.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\", \"PCE [%]\": \"14.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:BTP-4F:PC61BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.5\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"802.0\"}, {\"Refs.\": \"S. Liu, J. Yuan, W. Deng, M. Luo, Y. Xie, Q. Liang, Y. Zou, Z. He, H. Wu, Y. Cao, Nat. Photonics 2020, 14, 300.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y11\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.36\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"25.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"846.0\"}, {\"Refs.\": \"Y. Lin, M. I. Nugraha, Y. Firdaus, A. D. Scaccabarozzi, F. Ani\\u00e9s, A.-H. Emwas, E. Yengel, X. Zheng, J. Liu, W. Wahyudi, E. Yarali, H. Faber, O. M. Bakr, L. Tsetseris, M. Heeney, T. D. Anthopoulos, ACS Energy Lett. 2020, 5, 3663.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"26.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"856.0\"}, {\"Refs.\": \"L. Arunagiri, Z. Peng, X. Zou, H. Yu, G. Zhang, Z. Wang, J. Y. Lin Lai, J. Zhang, Y. Zheng, C. Cui, F. Huang, Y. Zou, K. S. Wong, P. C. Y. Chow, H. Ade, H. Yan, Joule 2020, 4, 1790.\", \"PCE [%]\": \"17.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:PTQ10:PC71BM:N3\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.7\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"852.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, J. Zhang, K. Xian, T. Zhang, L. Hong, Y. Wang, Y. Xu, K. Ma, C. An, C. He, Z. Wei, F. Gao, J. Hou, Adv. Mater. 2020, 32, 1908205.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-eC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.5\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"841.0\"}, {\"Refs.\": \"Q. Liu, Y. Jiang, K. Jin, J. Qin, J. Xu, W. Li, J. Xiong, J. Liu, Z. Xiao, K. Sun, S. Yang, X. Zhang, L. Ding, Sci. Bull. 2020, 65, 272.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"D18:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.6\", \"Jsc [mA cm\\u22122]\": \"27.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"859.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, L. Hong, T. Zhang, Y. Tang, B. Lin, K. Xian, B. Gao, C. An, P. Bi, W. Ma, J. Hou, Natl. Sci. Rev. 2019, 7, 1239.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-4Cl-12\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"25.5\", \"Jsc [mA cm\\u22122]\": \"77.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"858.0\"}, {\"Refs.\": \"H. Chen, H. Lai, Z. Chen, Y. Zhu, H. Wang, L. Han, Y. Zhang, F. He, Angew. Chem., Int. Ed. 2021, 60, 3238.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTIC-2Cl-\\u03b3CF3: PC71ThBM: PBDB-TF\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"25.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"X. Guo, Q. Fan, J. Wu, G. Li, Z. Peng, W. Su, J. Lin, L. Hou, Y. Qin, H. Ade, L. Ye, M. Zhang, Y. Li, Angew. Chem., Int. Ed. 2021, 60, 2322.\", \"PCE [%]\": \"17.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6-Tz20: Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"27.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"L. Liu, Y. Kan, K. Gao, J. Wang, M. Zhao, H. Chen, C. Zhao, T. Jiu, A.-K.-Y. Jen, Y. Li, Adv. Mater. 2020, 32, 1907604.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"26.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"834.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\", \"PCE [%]\": \"16.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"25.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"867.0\"}, {\"Refs.\": \"C. Xu, X. Ma, Z. Zhao, M. Jiang, Z. Hu, J. Gao, Z. Deng, Z. Zhou, Q. An, J. Zhang, F. Zhang, Sol. RRL 2021, 5, 2100175.\", \"PCE [%]\": \"17.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"D18-Cl:PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.8\", \"Jsc [mA cm\\u22122]\": \"26.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"871.0\"}, {\"Refs.\": \"X. Liao, Q. He, G. Zhou, X. Xia, P. Zhu, Z. Xing, H. Zhu, Z. Yao, X. Lu, Y. Chen, Chem. Mater. 2021, 33, 430.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6:DFBT-TT6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.0\", \"Jsc [mA cm\\u22122]\": \"26.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"845.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\", \"PCE [%]\": \"17.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.9\", \"Jsc [mA cm\\u22122]\": \"25.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"862.0\"}, {\"Refs.\": \"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Nat. Commun. 2019, 10, 2515.\", \"PCE [%]\": \"15.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTP-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.1\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"834.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\", \"PCE [%]\": \"15.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.4\", \"Jsc [mA cm\\u22122]\": \"25.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"838.0\"}, {\"Refs.\": \"Q. Guo, J. Lin, H. Liu, X. Dong, X. Guo, L. Ye, Z. Ma, Z. Tang, H. Ade, M. Zhang, Y. Li, Nano Energy 2020, 74, 104861.\", \"PCE [%]\": \"14.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:IDST-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"T. Liu, T. Yang, R. Ma, L. Zhan, Z. Luo, G. Zhang, Y. Li, K. Gao, Y. Xiao, J. Yu, X. Zou, H. Sun, M. Zhang, T. A. Dela Pe\\u00f1a, Z. Xing, H. Liu, X. Li, G. Li, J. Huang, C. Duan, K. S. Wong, X. Lu, X. Guo, F. Gao, H. Chen, F. Huang, Y. Li, Y. Li, Y. Cao, B. Tang, H. Yan, Joule 2021, 5, 914.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:PY-IT:BN-T\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"144.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.3\", \"Jsc [mA cm\\u22122]\": \"22.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"955.0\"}, {\"Refs.\": \"H. Lai, Q. Zhao, Z. Chen, H. Chen, P. Chao, Y. Zhu, Y. Lang, N. Zhen, D. Mo, Y. Zhang, F. He, Joule 2020, 4, 688.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:BTIC-F-m\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.1\", \"Jsc [mA cm\\u22122]\": \"21.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"M. Green, E. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 3.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"25.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"897.0\"}, {\"Refs.\": \"K. Jiang, Q. Wei, J. Y. L. Lai, Z. Peng, H. K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Joule 2019, 3, 3020.\", \"PCE [%]\": \"12.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:N-C11\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.6\", \"Jsc [mA cm\\u22122]\": \"21.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"852.0\"}, {\"Refs.\": \"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\", \"PCE [%]\": \"14.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:BP-4F:MF1\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.47\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"23.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"882.0\"}, {\"Refs.\": \"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:IDT-EDOT:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.48\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.7\", \"Jsc [mA cm\\u22122]\": \"20.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\", \"PCE [%]\": \"15.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:DTTC-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"22.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\", \"PCE [%]\": \"13.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:SeTlC4Cl-DIO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.51\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:IDT-EDOT:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"18.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:SeTlC4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.7\", \"Jsc [mA cm\\u22122]\": \"22.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTR:NITI:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.8\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.3\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"826.0\"}, {\"Refs.\": \"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\", \"PCE [%]\": \"13.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:DTTC-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.4\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"950.0\"}, {\"Refs.\": \"Y. Lin, B. Adilbekova, Y. Firdaus, E. Yengel, H. Faber, M. Sajjad, X. Zheng, E. Yarali, A. Seitkhan, O. M. Bakr, A. El-Labban, U. Schwingenschl\\u00f6gl, V. Tung, I. McCulloch, F. Laquai, T. D. Anthopoulos, Adv. Mater. 2019, 31, 1902965.\", \"PCE [%]\": \"13.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-SF:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.53\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"T.-W. Chen, K.-L. Peng, Y.-W. Lin, Y.-J. Su, K.-J. Ma, L. Hong, C.-C. Chang, J. Hou, C.-S. Hsu, J. Mater. Chem. A 2020, 8, 1131.\", \"PCE [%]\": \"13.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:DTC-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.5\", \"Jsc [mA cm\\u22122]\": \"20.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"J. Gao, W. Gao, X. Ma, Z. Hu, C. Xu, X. Wang, Q. An, C. Yang, X. Zhang, F. Zhang, Energy Environ. Sci. 2020, 13, 958.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:MF1\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"916.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.5\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"793.0\"}, {\"Refs.\": \"Z. Luo, C. Sun, S. Chen, Z.-G. Zhang, K. Wu, B. Qiu, C. Yang, Y. Li, C. Yang, Adv. Energy Mater. 2018, 8, 1800856.\", \"PCE [%]\": \"12.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTQ10:IDTPC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"930.0\"}, {\"Refs.\": \"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTQ10:IDIC-2F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.6\", \"Jsc [mA cm\\u22122]\": \"19.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"910.0\"}, {\"Refs.\": \"F. Pan, C. Sun, Y. Li, D. Tang, Y. Zou, X. Li, S. Bai, X. Wei, M. Lv, X. Chen, Y. Li, Energy Environ. Sci. 2019, 12, 3400.\", \"PCE [%]\": \"12.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTQ10:IDIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.3\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\", \"PCE [%]\": \"9.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"J51:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.7\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.2\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"815.0\"}, {\"Refs.\": \"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, ACS Energy Lett. 2018, 3, 2967.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"P4TIF:PC61BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.9\", \"Jsc [mA cm\\u22122]\": \"21.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2016, 24, 3.\", \"PCE [%]\": \"11.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.7\", \"Jsc [mA cm\\u22122]\": \"19.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"791.0\"}, {\"Refs.\": \"D. Baran, N. Gasparini, A. Wadsworth, C. H. Tan, N. Wehbe, X. Song, Z. Hamid, W. Zhang, M. Neophytou, T. Kirchartz, C. J. Brabec, J. R. Durrant, I. McCulloch, Nat. Commun. 2018, 9, 2059.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDTTT-EFT:EHIDTBR\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"18.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"C. Li, J. Song, Y. Cai, G. Han, W. Zheng, Y. Yi, H. S. Ryu, H. Y. Woo, Y. Sun, J. Energy Chem. 2020, 40, 144.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBT1-C:NFA\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.9\", \"Jsc [mA cm\\u22122]\": \"13.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"878.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\", \"PCE [%]\": \"11.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"867.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \" \", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.72\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.4\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"899.0\"}, {\"Refs.\": \"L. Q. Phuong, S. M. Hosseini, C. W. Koh, H. Y. Woo, S. Shoaee, J. Phys. Chem. C 2019, 123, 27417.\", \"PCE [%]\": \"9.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PPDT2FBT:PC70BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.78\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"17.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"786.0\"}, {\"Refs.\": \"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BDT-ffBX-DT:PDI4\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.1\", \"Jsc [mA cm\\u22122]\": \"10.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C. J. Brabec, F. Huang, Y. Cao, Adv. Energy Mater. 2018, 8, 1801699.\", \"PCE [%]\": \"6.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BDT-ffBX-DT:SFPDI\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.6\", \"Jsc [mA cm\\u22122]\": \"8.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1230.0\"}, {\"Refs.\": \"Z. Zhou, S. Xu, J. Song, Y. Jin, Q. Yue, Y. Qian, F. Liu, F. Zhang, X. Zhu, Nat. Energy 2018, 3, 952.\", \"PCE [%]\": \"9.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTR:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.9\", \"Jsc [mA cm\\u22122]\": \"13.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"900.0\"}, {\"Refs.\": \"C. e. Zhang, P. Jiang, X. Zhou, H. Liu, Q. Guo, X. Xu, Y. Liu, Z. Tang, W. Ma, Z. Bo, J. Mater. Chem. A 2020, 8, 2123.\", \"PCE [%]\": \"7.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.1\", \"Jsc [mA cm\\u22122]\": \"13.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"M. Li, H. Wang, Y. Liu, Y. Zhou, H. Lu, J. Song, Z. Bo, Dyes Pigm. 2020, 175, 108186.\", \"PCE [%]\": \"7.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:NDP-Se-DIO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.9\", \"Jsc [mA cm\\u22122]\": \"12.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"L. Ma, Y. Xu, Y. Zu, Q. Liao, B. Xu, C. An, S. Zhang, J. Hou, Sci. China Chem. 2020, 63, 21.\", \"PCE [%]\": \"5.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2Cl:PC61BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"55.9\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"950.0\"}, {\"Refs.\": \"A. Abdul Raheem, C. Kumar, P. Murugan, C. Praveen, ACS Appl. Energy Mater. 2021, 4, 11609.\", \"PCE [%]\": \"6.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"P3HT:TCBD14\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.93\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.3\", \"Jsc [mA cm\\u22122]\": \"12.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"790.0\"}, {\"Refs.\": \"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\", \"PCE [%]\": \"3.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"P3HT:PCBM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.2\", \"Jsc [mA cm\\u22122]\": \"10.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"592.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.3\", \"Jsc [mA cm\\u22122]\": \"21.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \" \", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"714.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2012, 20, 12.\", \"PCE [%]\": \"11.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"21.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \" \", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"743.0\"}, {\"Refs.\": \"T.-K. Chang, Y. Chi, RSC Adv. 2017, 7, 42013.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.9\", \"Jsc [mA cm\\u22122]\": \"18.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TF-tBu_C3F7\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"C.-C. Chen, J.-S. Chen, V. S. Nguyen, T.-C. Wei, C.-Y. Yeh, Angew. Chem., Int. Ed. 2021, 60, 4886.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.9\", \"Jsc [mA cm\\u22122]\": \"16.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"bJS2\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"849.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.7\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"YD2\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"694.0\"}, {\"Refs.\": \"M. Godfroy, J. Liotier, V. M. Mwalukuku, D. Joly, Q. Huaulm\\u00e9, L. Cabau, C. Aumaitre, Y. Kervella, S. Narbey, F. Oswald, E. Palomares, C. A. Gonz\\u00e1lez Flores, G. Oskam, R. Demadrille, Sustainable Energy Fuels 2021, 5, 144.\", \"PCE [%]\": \"10.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.75\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"20.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"YKP-88/YKP-137 (6/4)\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"745.0\"}, {\"Refs.\": \"Z. Ge, C. Wang, Z. Chen, T. Wang, T. Chen, R. Shi, S. Yu, J. Liu, Mater. Res. Bull. 2021, 135, 111148.\", \"PCE [%]\": \"8.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.76\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.3\", \"Jsc [mA cm\\u22122]\": \"17.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TNA\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"700.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"740.0\"}, {\"Refs.\": \"E. Akman, S. Akin, T. Ozturk, B. Gulveren, S. Sonmezoglu, Sol. Energy 2020, 202, 227.\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.0\", \"Jsc [mA cm\\u22122]\": \"19.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"744.0\"}, {\"Refs.\": \"C. Wang, X. Zhang, D. Cao, H. Yin, X. Li, P. Cheng, B. Mi, Z. Gao, W. Deng, Org. Electron. 2017, 49, 135.\", \"PCE [%]\": \"9.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.2\", \"Jsc [mA cm\\u22122]\": \"19.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"790.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Liu, H.-H. Chou, K. Kala, T.-C. Wei, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 39970.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.5\", \"Jsc [mA cm\\u22122]\": \"13.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SK7\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"663.0\"}, {\"Refs.\": \"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\", \"PCE [%]\": \"6.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.8\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"AN-11\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"D. Cao, X. Li, X. Yu, N. Cheng, P. Yang, B. Mi, Z. Gao, Phys. Status Solidi A 2020, 217, 1900724.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.5\", \"Jsc [mA cm\\u22122]\": \"19.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2020, 28, 3.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"15.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \" \", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"8.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"14.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"782.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321.\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.7\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"L351\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TY4\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"730.0\"}, {\"Refs.\": \"X. Wang, A. Bolag, W. Yun, Y. Du, C. Eerdun, X. Zhang, T. Bao, J. Ning, H. Alata, T. Ojiyed, J. Mol. Struct. 2020, 1206, 127694.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.89\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.8\", \"Jsc [mA cm\\u22122]\": \"21.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719+W2\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"580.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.93\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"13.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"L350\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\", \"PCE [%]\": \"3.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.97\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"6.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"AN-14\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"600.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"5.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.99\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.5\", \"Jsc [mA cm\\u22122]\": \"11.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SK6\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"689.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"6.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"12.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"CW10+SK6\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"732.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.1\", \"Jsc [mA cm\\u22122]\": \"11.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"L349\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1160.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.02\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TY6\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"M.-C. Tsai, C.-L. Wang, C.-W. Chang, C.-W. Hsu, Y.-H. Hsiao, C.-L. Liu, C.-C. Wang, S.-Y. Lin, C.-Y. Lin, J. Mater. Chem. A 2018, 6, 1995.\", \"PCE [%]\": \"3.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"7.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"AN-12\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.3\", \"Jsc [mA cm\\u22122]\": \"11.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TY3\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"K. S. K. Reddy, Y.-C. Chen, C.-C. Wu, C.-W. Hsu, Y.-C. Chang, C.-M. Chen, C.-Y. Yeh, ACS Appl. Mater. Interfaces 2018, 10, 2391.\", \"PCE [%]\": \"5.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.12\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.7\", \"Jsc [mA cm\\u22122]\": \"10.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"CW10\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"739.0\"}, {\"Refs.\": \"Y. S. Tingare, N. S. n. Vinh, H.-H. Chou, Y.-C. Liu, Y.-S. Long, T.-C. Wu, T.-C. Wei, C.-Y. Yeh, Adv. Energy Mater. 2017, 7, 1700032.\", \"PCE [%]\": \"5.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.8\", \"Jsc [mA cm\\u22122]\": \"10.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"MS3\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"Y. Liu, Y. Cao, W. Zhang, M. Stojanovic, M. I. Dar, P. P\\u00e9chy, Y. Saygili, A. Hagfeldt, S. M. Zakeeruddin, M. Gr\\u00e4tzel, Angew. Chem. 2018, 130, 14321.\", \"PCE [%]\": \"5.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"6.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"L348\", \"Table\": \"ver2_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"R. Sun, D. Zhuang, M. Zhao, Q. Gong, M. Scarpulla, Y. Wei, G. Ren, Y. Wu, Sol. Energy Mater. Sol. Cells 2018, 174, 494.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(Se,S)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"0.98\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"39.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"430.0\"}, {\"Refs.\": \"J. Li, J. Huang, K. Li, Y. Zeng, Y. Zhang, K. Sun, C. Yan, C. Xue, C. Chen, T. Chen, M. A. Green, J. Tang, X. Hao, Sol. RRL 2021, 5, 2000693.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.02\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.4\", \"Jsc [mA cm\\u22122]\": \"39.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"441.0\"}, {\"Refs.\": \"Y. S. Lee, T. Gershon, O. Gunawan, T. K. Todorov, T. Gokmen, Y. Virgus, S. Guha, Adv. Energy Mater. 2015, 5, 1401372.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.03\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.3\", \"Jsc [mA cm\\u22122]\": \"40.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"423.0\"}, {\"Refs.\": \"H. Tampo, K. M. Kim, S. Kim, H. Shibata, S. Niki, J. Appl. Phys. 2017, 122, 023106.\", \"PCE [%]\": \"9.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.04\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.5\", \"Jsc [mA cm\\u22122]\": \"34.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"425.0\"}, {\"Refs.\": \"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcob\\u00e9, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. P\\u00e9rez-Rodr\\u00edguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\", \"PCE [%]\": \"9.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.3\", \"Jsc [mA cm\\u22122]\": \"32.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"457.0\"}, {\"Refs.\": \"S. Giraldo, E. Saucedo, M. Neuschitzer, F. Oliva, M. Placidi, X. Alcob\\u00e9, V. Izquierdo-Roca, S. Kim, H. Tampo, H. Shibata, A. P\\u00e9rez-Rodr\\u00edguez, P. Pistor, Energy Environ. Sci. 2018, 11, 582.\", \"PCE [%]\": \"9.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.06\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.4\", \"Jsc [mA cm\\u22122]\": \"31.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"460.0\"}, {\"Refs.\": \"J. Zhou, X. Xu, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Nano Energy 2021, 89, 106405.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.06\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.0\", \"Jsc [mA cm\\u22122]\": \"40.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"477.0\"}, {\"Refs.\": \"J. Zhou, X. Xu, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Nano Energy 2021, 89, 106405.\", \"PCE [%]\": \"11.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.06\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"36.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"461.0\"}, {\"Refs.\": \"J. Li, Y. Huang, J. Huang, G. Liang, Y. Zhang, G. Rey, F. Guo, Z. Su, H. Zhu, L. Cai, K. Sun, Y. Sun, F. Liu, S. Chen, X. Hao, Y. Mai, M. A. Green, Adv. Mater. 2020, 32, 2005268.\", \"PCE [%]\": \"12.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.07\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"37.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"491.0\"}, {\"Refs.\": \"Y. Gong, Y. Zhang, E. Jedlicka, R. Giridharagopal, J. A. Clark, W. Yan, C. Niu, R. Qiu, J. Jiang, S. Yu, S. Wu, H. W. Hillhouse, D. S. Ginger, W. Huang, H. Xin, Sci. China Mater. 2021, 64, 52.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.08\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.3\", \"Jsc [mA cm\\u22122]\": \"33.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"522.0\"}, {\"Refs.\": \"Y. Gong, Y. Zhang, E. Jedlicka, R. Giridharagopal, J. A. Clark, W. Yan, C. Niu, R. Qiu, J. Jiang, S. Yu, S. Wu, H. W. Hillhouse, D. S. Ginger, W. Huang, H. Xin, Sci. China Mater. 2021, 64, 52.\", \"PCE [%]\": \"12.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.8\", \"Jsc [mA cm\\u22122]\": \"37.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"475.0\"}, {\"Refs.\": \"Y. Gong, R. Qiu, C. Niu, J. Fu, E. Jedlicka, R. Giridharagopal, Q. Zhu, Y. Zhou, W. Yan, S. Yu, J. Jiang, S. Wu, D. S. Ginger, W. Huang, H. Xin, Adv. Funct. Mater. 2021, 31, 2101927.\", \"PCE [%]\": \"12.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"(Ag,Cu)2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.1\", \"Jsc [mA cm\\u22122]\": \"32.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"540.0\"}, {\"Refs.\": \"J. Lee, T. Enkhbat, G. Han, M. H. Sharif, E. Enkhbayar, H. Yoo, J. H. Kim, S. Kim, J. Kim, Nano Energy 2020, 78, 105206.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.1\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.3\", \"Jsc [mA cm\\u22122]\": \"36.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"445.0\"}, {\"Refs.\": \"Y. Gong, Y. Zhang, E. Jedlicka, R. Giridharagopal, J. A. Clark, W. Yan, C. Niu, R. Qiu, J. Jiang, S. Yu, S. Wu, H. W. Hillhouse, D. S. Ginger, W. Huang, H. Xin, Sci. China Mater. 2021, 64, 52.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.4\", \"Jsc [mA cm\\u22122]\": \"32.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"520.0\"}, {\"Refs.\": \"S. Kim, K. M. Kim, H. Tampo, H. Shibata, S. Niki, Appl. Phys. Express 2016, 9, 102301.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2Zn(Sn0.78Ge0.22)Se4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.12\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"32.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"527.0\"}, {\"Refs.\": \"W. Wang, M. T. Winkler, O. Gunawan, T. Gokmen, T. K. Todorov, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2014, 4, 1301465.\", \"PCE [%]\": \"12.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.13\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.8\", \"Jsc [mA cm\\u22122]\": \"35.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"513.0\"}, {\"Refs.\": \"T. K. Todorov, J. Tang, S. Bag, O. Gunawan, T. Gokmen, Y. Zhu, D. B. Mitzi, Adv. Energy Mater. 2013, 3, 34.\", \"PCE [%]\": \"11.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.13\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.8\", \"Jsc [mA cm\\u22122]\": \"34.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"460.0\"}, {\"Refs.\": \"D.-H. Son, S.-H. Kim, S.-Y. Kim, Y.-I. Kim, J.-H. Sim, S.-N. Park, D.-H. Jeon, D.-K. Hwang, S.-J. Sung, J.-K. Kang, K.-J. Yang, D.-H. Kim, J. Mater. Chem. A 2019, 7, 25279.\", \"PCE [%]\": \"12.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.14\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.9\", \"Jsc [mA cm\\u22122]\": \"35.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"541.0\"}, {\"Refs.\": \"K.-J. Yang, S. Kim, S.-Y. Kim, D.-H. Son, J. Lee, Y.-I. Kim, S.-J. Sung, D.-H. Kim, T. Enkhbat, J. Kim, J. Kim, W. Jo, J.-K. Kang, Adv. Funct. Mater. 2021, n/a, 2102238.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.16\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.8\", \"Jsc [mA cm\\u22122]\": \"33.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"539.0\"}, {\"Refs.\": \"K. Shen, Y. Zhang, X. Wang, C. Ou, F. Guo, H. Zhu, C. Liu, Y. Gao, R. E. I. Schropp, Z. Li, X. Liu, Y. Mai, Adv. Sci. 2020, n/a, 2001013.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.22\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.4\", \"Jsc [mA cm\\u22122]\": \"28.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"413.0\"}, {\"Refs.\": \"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.24\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.6\", \"Jsc [mA cm\\u22122]\": \"32.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"400.0\"}, {\"Refs.\": \"Z. Li, X. Liang, G. Li, H. Liu, H. Zhang, J. Guo, J. Chen, K. Shen, X. San, W. Yu, R. E. I. Schropp, Y. Mai, Nat. Commun. 2019, 10, 125.\", \"PCE [%]\": \"4.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.27\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"47.3\", \"Jsc [mA cm\\u22122]\": \"27.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"370.0\"}, {\"Refs.\": \"S. Wen, X. Yin, C. Zhang, Y. Guo, J. Liu, E. Wang, C. Zheng, W. Que, H. Liu, W. Liu, Mater. Lett. 2021, 283, 128770.\", \"PCE [%]\": \"4.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.29\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"51.0\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"340.0\"}, {\"Refs.\": \"K. Li, F. Li, C. Chen, P. Jiang, S. Lu, S. Wang, Y. Lu, G. Tu, J. Guo, L. Shui, Z. Liu, B. Song, J. Tang, Nano Energy 2021, 86, 106101.\", \"PCE [%]\": \"7.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.7\", \"Jsc [mA cm\\u22122]\": \"29.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"420.0\"}, {\"Refs.\": \"J. Li, J. Huang, K. Li, Y. Zeng, Y. Zhang, K. Sun, C. Yan, C. Xue, C. Chen, T. Chen, M. A. Green, J. Tang, X. Hao, Sol. RRL 2021, 5, 2000693.\", \"PCE [%]\": \"6.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"54.7\", \"Jsc [mA cm\\u22122]\": \"27.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"421.0\"}, {\"Refs.\": \"L. Choubrac, M. B\\u00e4r, X. Kozina, R. F\\u00e9lix, R. G. Wilks, G. Brammertz, S. Levcenko, L. Arzel, N. Barreau, S. Harel, M. Meuris, B. Vermang, ACS Appl. Energy Mater. 2020, 3, 5830.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnGeSe4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"55.7\", \"Jsc [mA cm\\u22122]\": \"24.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"625.0\"}, {\"Refs.\": \"C. Yan, J. Huang, K. Sun, S. Johnston, Y. Zhang, H. Sun, A. Pu, M. He, F. Liu, K. Eder, L. Yang, J. M. Cairney, N. J. Ekins-Daukes, Z. Hameiri, J. A. Stride, S. Chen, M. A. Green, X. Hao, Nat. Energy 2018, 3, 764.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSnS4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.3\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"731.0\"}, {\"Refs.\": \"R. Tang, X. Wang, W. Lian, J. Huang, Q. Wei, M. Huang, Y. Yin, C. Jiang, S. Yang, G. Xing, S. Chen, C. Zhu, X. Hao, M. A. Green, T. Chen, Nat. Energy 2020, 5, 587.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2(S,Se)3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.3\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"655.0\"}, {\"Refs.\": \"K. Timmo, M. Altosaar, M. Pilvet, V. Mikli, M. Grossberg, M. Danilson, T. Raadik, R. Josepson, J. Krustok, M. Kauk-Kuusik, J. Mater. Chem. A 2019, 7, 24281.\", \"PCE [%]\": \"8.73\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"(Cu0.99Ag0.01)1.85(Zn0.8Cd0.2)1.1SnS4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.9\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"664.0\"}, {\"Refs.\": \"R. Nie, M. Hu, A. M. Risqi, Z. Li, S. I. Seok, Adv. Sci. 2021, 8, 2003172.\", \"PCE [%]\": \"4.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"SbSeI:Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.7\", \"Jsc [mA cm\\u22122]\": \"14.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"473.0\"}, {\"Refs.\": \"Y. C. Choi, D. U. Lee, J. H. Noh, E. K. Kim, S. I. Seok, Adv. Funct. Mater. 2014, 24, 3587.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2S3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.0\", \"Jsc [mA cm\\u22122]\": \"16.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"711.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2014, 22, 1.\", \"PCE [%]\": \"19.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.09\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"34.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"716.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\", \"PCE [%]\": \"21.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.1\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.3\", \"Jsc [mA cm\\u22122]\": \"40.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"718.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. H. Ho-Baillie, Prog. Photovoltaics 2017, 25, 668.\", \"PCE [%]\": \"26.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (crystalline)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.9\", \"Jsc [mA cm\\u22122]\": \"42.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"738.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2018, 26, 427.\", \"PCE [%]\": \"22.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.13\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.5\", \"Jsc [mA cm\\u22122]\": \"38.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"744.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 805.\", \"PCE [%]\": \"21.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.14\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"35.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"757.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2019, 27, 565.\", \"PCE [%]\": \"23.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.15\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.4\", \"Jsc [mA cm\\u22122]\": \"39.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"734.0\"}, {\"Refs.\": \"W. Li, S. Xu, Y. Dai, P. Ma, Y. Feng, W. Li, H. Luo, C. Yang, Mater. Lett. 2019, 244, 43.\", \"PCE [%]\": \"16.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.1\", \"Jsc [mA cm\\u22122]\": \"31.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"762.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, M. Yoshita, A. W. Y. Ho-Baillie, Prog. Photovoltaics Res. Appl. 2019, 27, 3.\", \"PCE [%]\": \"29.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"GaAs\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"86.7\", \"Jsc [mA cm\\u22122]\": \"29.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1127.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\", \"PCE [%]\": \"21.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"30.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"876.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.48\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"27.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"857.0\"}, {\"Refs.\": \"S. Shukla, M. Sood, D. Adeleye, S. Peedle, G. Kusch, D. Dahliah, M. Melchiorre, G.-M. Rignanese, G. Hautier, R. Oliver, S. Siebentritt, Joule 2021, 5, 1816.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"23.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"902.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2015, 23, 1.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (amorphous)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.8\", \"Jsc [mA cm\\u22122]\": \"16.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"896.0\"}, {\"Refs.\": \"T. Matsui, A. Bidiville, K. Maejima, H. Sai, T. Koida, T. Suezaki, M. Matsumoto, K. Saito, I. Yoshida, M. Kondo, Appl. Phys. Lett. 2015, 106, 053901.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (amorphous)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"16.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"896.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, Prog. Photovoltaics 2010, 18, 346.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si (amorphous)\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.0\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"886.0\"}, {\"Refs.\": \"F. Sahli, J. Werner, B. A. Kamino, M. Br\\u00e4uninger, R. Monnard, B. Paviet-Salomon, L. Barraud, L. Ding, J. J. Diaz Leon, D. Sacchetto, G. Cattaneo, M. Despeisse, M. Boccard, S. Nicolay, Q. Jeangros, B. Niesen, C. Ballif, Nat. Mater. 2018, 17, 820.\", \"PCE [%]\": \"24.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.63\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.1\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"CsxFA1\\u2212xPb(I,Br)3\", \"Voc [mV]\": \"1786.0\"}, {\"Refs.\": \"B. Chen, Z. J. Yu, S. Manzoor, S. Wang, W. Weigand, Z. Yu, G. Yang, Z. Ni, X. Dai, Z. C. Holman, J. Huang, Joule 2020, 4, 850.\", \"PCE [%]\": \"26.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.66\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.4\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.1MA0.9PbI2.7Br0.3\", \"Voc [mV]\": \"1820.0\"}, {\"Refs.\": \"D. Kim, H. J. Jung, I. J. Park, B. W. Larson, S. P. Dunfield, C. Xiao, J. Kim, J. Tong, P. Boonmongkolras, S. G. Ji, F. Zhang, S. R. Pae, M. Kim, S. B. Kang, V. Dravid, J. J. Berry, J. Y. Kim, K. Zhu, D. H. Kim, B. Shin, Science 2020, 368, 155.\", \"PCE [%]\": \"26.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.67\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"PEA(I0.25SCN0.75)\", \"Voc [mV]\": \"1756.0\"}, {\"Refs.\": \"Y. Hou, E. Aydin, M. De Bastiani, C. Xiao, F. H. Isikgor, D.-J. Xue, B. Chen, H. Chen, B. Bahrami, A. H. Chowdhury, A. Johnston, S.-W. Baek, Z. Huang, M. Wei, Y. Dong, J. Troughton, R. Jalmood, A. J. Mirabelli, T. G. Allen, E. Van Kerschaver, M. I. Saidaminov, D. Baran, Q. Qiao, K. Zhu, S. De Wolf, E. H. Sargent, Science 2020, 367, 1135.\", \"PCE [%]\": \"25.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.68\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.4\", \"Jsc [mA cm\\u22122]\": \"19.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.05MA0.15FA0.8PbI2.25Br0.75\", \"Voc [mV]\": \"1781.0\"}, {\"Refs.\": \"M. De Bastiani, A. J. Mirabelli, Y. Hou, F. Gota, E. Aydin, T. G. Allen, J. Troughton, A. S. Subbiah, F. H. Isikgor, J. Liu, L. Xu, B. Chen, E. Van Kerschaver, D. Baran, B. Fraboni, M. F. Salvador, U. W. Paetzold, E. H. Sargent, S. De Wolf, Nat. Energy 2021, 6, 167.\", \"PCE [%]\": \"25.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.68\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \" \", \"Voc [mV]\": \"1800.0\"}, {\"Refs.\": \"E. K\\u00f6hnen, M. Jo\\u0161t, A. B. Morales-Vilches, P. Tockhorn, A. Al-Ashouri, B. Macco, L. Kegelmann, L. Korte, B. Rech, R. Schlatmann, B. Stannowski, S. Albrecht, Sustainable Energy Fuels 2019, 3, 1995.\", \"PCE [%]\": \"26.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.64\", \"Eg,bottom [eV]\": \"1.12\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.5\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.83MA0.17PbI3\", \"Voc [mV]\": \"1760.0\"}, {\"Refs.\": \"M. Jo\\u0161t, E. K\\u00f6hnen, A. B. Morales-Vilches, B. Lipov\\u0161ek, K. J\\u00e4ger, B. Macco, A. Al-Ashouri, J. Kr\\u010d, L. Korte, B. Rech, R. Schlatmann, M. Topi\\u010d, B. Stannowski, S. Albrecht, Energy Environ. Sci. 2018, 11, 3511.\", \"PCE [%]\": \"26.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.65\", \"Eg,bottom [eV]\": \"1.12\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.05MA0.16FA0.79PbI2.49Br0.51\", \"Voc [mV]\": \"1760.0\"}, {\"Refs.\": \"A. Al-Ashouri, E. K\\u00f6hnen, B. Li, A. Magomedov, H. Hempel, P. Caprioglio, J. A. M\\u00e1rquez, A. B. Morales Vilches, E. Kasparavicius, J. A. Smith, N. Phung, D. Menzel, M. Grischek, L. Kegelmann, D. Skroblin, C. Gollwitzer, T. Malinauskas, M. Jo\\u0161t, G. Mati\\u010d, B. Rech, R. Schlatmann, M. Topi\\u010d, L. Korte, A. Abate, B. Stannowski, D. Neher, M. Stolterfoht, T. Unold, V. Getautis, S. Albrecht, Science 2020, 370, 1300.\", \"PCE [%]\": \"28.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.68\", \"Eg,bottom [eV]\": \"1.12\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.05FA0.73MA0.22PbI2.31Br0.69\", \"Voc [mV]\": \"1895.0\"}, {\"Refs.\": \"G. Nogay, F. Sahli, J. Werner, R. Monnard, M. Boccard, M. Despeisse, F. J. Haug, Q. Jeangros, A. Ingenito, C. Ballif, ACS Energy Lett. 2019, 4, 844.\", \"PCE [%]\": \"24.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.65\", \"Eg,bottom [eV]\": \"1.13\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"CsFAPb(IBr)3\", \"Voc [mV]\": \"1735.0\"}, {\"Refs.\": \"J. Xu, C. C. Boyd, Z. J. Yu, A. F. Palmstrom, D. J. Witter, B. W. Larson, R. M. France, J. Werner, S. P. Harvey, E. J. Wolf, W. Weigand, S. Manzoor, M. F. A. M. van Hest, J. J. Berry, J. M. Luther, Z. C. Holman, M. D. McGehee, Science 2020, 367, 1097.\", \"PCE [%]\": \"27.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.67\", \"Eg,bottom [eV]\": \"1.13\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.3\", \"Jsc [mA cm\\u22122]\": \"19.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"CsFAMAPb(IBrCl)3\", \"Voc [mV]\": \"1886.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics Res. Appl. 2021, 29, 657.\", \"PCE [%]\": \"29.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.69\", \"Eg,bottom [eV]\": \"1.13\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \" \", \"Voc [mV]\": \"1884.0\"}, {\"Refs.\": \"J. Werner, C.-H. Weng, A. Walter, L. Fesquet, J. P. Seif, S. De Wolf, B. Niesen, C. Ballif, J. Phys. Chem. Lett. 2016, 7, 161.\", \"PCE [%]\": \"20.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.62\", \"Eg,bottom [eV]\": \"1.15\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"MAPI\", \"Voc [mV]\": \"1690.0\"}, {\"Refs.\": \"B. Chen, Z. Yu, K. Liu, X. Zheng, Y. Liu, J. Shi, D. Spronk, P. N. Rudd, Z. Holman, J. Huang, Joule 2019, 3, 177.\", \"PCE [%]\": \"25.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.68\", \"Eg,bottom [eV]\": \"1.15\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.15FA0.71MA0.14PbI2.4Br0.6\", \"Voc [mV]\": \"1800.0\"}, {\"Refs.\": \"K. A. Bush, S. Manzoor, K. Frohna, Z. J. Yu, J. A. Raiford, A. F. Palmstrom, H.-P. Wang, R. Prasanna, S. F. Bent, Z. C. Holman, M. D. McGehee, ACS Energy Lett. 2018, 3, 2173.\", \"PCE [%]\": \"25.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.68\", \"Eg,bottom [eV]\": \"1.15\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.75Cs0.25PbI2.4Br0.6\", \"Voc [mV]\": \"1770.0\"}, {\"Refs.\": \"J. Werner, C.-H. Weng, A. Walter, L. Fesquet, J. P. Seif, S. De Wolf, B. Niesen, C. Ballif, J. Phys. Chem. Lett. 2016, 7, 161.\", \"PCE [%]\": \"19.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.62\", \"Eg,bottom [eV]\": \"1.16\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"16.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"MAPI\", \"Voc [mV]\": \"1701.0\"}, {\"Refs.\": \"Z. Li, T. H. Kim, S. Y. Han, Y.-J. Yun, S. Jeong, B. Jo, S. A. Ok, W. Yim, S. H. Lee, K. Kim, S. Moon, J.-Y. Park, T. K. Ahn, H. Shin, J. Lee, H. J. Park, Adv. Energy Mater. 2020, 10, 1903085.\", \"PCE [%]\": \"24.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"GaAs\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.85\", \"Eg,bottom [eV]\": \"1.42\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.8\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.80MA0.04Cs0.16Pb(I0.50Br0.50)3\", \"Voc [mV]\": \"2160.0\"}, {\"Refs.\": \"Q. Han, Y.-T. Hsieh, L. Meng, J.-L. Wu, P. Sun, E.-P. Yao, S.-Y. Chang, S.-H. Bae, T. Kato, V. Bermudez, Y. Yang, Science 2018, 361, 904.\", \"PCE [%]\": \"22.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CIGS\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.65\", \"Eg,bottom [eV]\": \"1.1\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.1\", \"Jsc [mA cm\\u22122]\": \"17.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.09FA0.77MA0.14Pb(I0.86Br0.14)3\", \"Voc [mV]\": \"1774.0\"}, {\"Refs.\": \"M. Jo\\u0161t, T. Bertram, D. Koushik, J. A. Marquez, M. A. Verheijen, M. D. Heinemann, E. K\\u00f6hnen, A. Al-Ashouri, S. Braunger, F. Lang, B. Rech, T. Unold, M. Creatore, I. Lauermann, C. A. Kaufmann, R. Schlatmann, S. Albrecht, ACS Energy Lett. 2019, 4, 583.\", \"PCE [%]\": \"21.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CIGS\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.64\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.0\", \"Jsc [mA cm\\u22122]\": \"18.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.05(MA0.17FA0.83)Pb1.1(I0.83Br0.17)3\", \"Voc [mV]\": \"1580.0\"}, {\"Refs.\": \"A. Al-Ashouri, A. Magomedov, M. Ro\\u00df, M. Jo\\u0161t, M. Talaikis, G. Chistiakova, T. Bertram, J. A. M\\u00e1rquez, E. K\\u00f6hnen, E. Kasparavi\\u010dius, S. Levcenco, L. Gil-Escrig, C. J. Hages, R. Schlatmann, B. Rech, T. Malinauskas, T. Unold, C. A. Kaufmann, L. Korte, G. Niaura, V. Getautis, S. Albrecht, Energy Environ. Sci. 2019, 12, 3356.\", \"PCE [%]\": \"23.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CIGS\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.65\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.05(MA0.17FA0.83)0.95Pb(I0.83Br0.17)3\", \"Voc [mV]\": \"1680.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2020, 28, 629.\", \"PCE [%]\": \"24.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CIGS\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.68\", \"Eg,bottom [eV]\": \"1.12\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.9\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \" \", \"Voc [mV]\": \"1768.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics Res. Appl. 2021, 29, 657.\", \"PCE [%]\": \"26.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \" \", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.81\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.9\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \" \", \"Voc [mV]\": \"2048.0\"}, {\"Refs.\": \"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\", \"PCE [%]\": \"24.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FSA:MA0.3FA0.7Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.6\", \"Jsc [mA cm\\u22122]\": \"15.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8Cs0.2Pb(I0.6Br0.4)3\", \"Voc [mV]\": \"1986.0\"}, {\"Refs.\": \"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\", \"PCE [%]\": \"25.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FSA:MA0.3FA0.7Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.8\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8Cs0.2Pb(I0.6Br0.4)3\", \"Voc [mV]\": \"2009.0\"}, {\"Refs.\": \"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\", \"PCE [%]\": \"22.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"(FASnI3)0.6(MAPbI3)0.4\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.72\", \"Eg,bottom [eV]\": \"1.27\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.8\", \"Jsc [mA cm\\u22122]\": \"15.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.05FA0.8MA0.15PbI2.55Br0.45\", \"Voc [mV]\": \"1915.0\"}, {\"Refs.\": \"Z. Yu, Z. Yang, Z. Ni, Y. Shao, B. Chen, Y. Lin, H. Wei, Z. J. Yu, Z. Holman, J. Huang, Nat. Energy 2020, 5, 657.\", \"PCE [%]\": \"24.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Cs0.05MA0.45FA0.5Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.81\", \"Eg,bottom [eV]\": \"1.27\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.8\", \"Jsc [mA cm\\u22122]\": \"15.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.4FA0.6PbI1.95Br1.05\", \"Voc [mV]\": \"2030.0\"}, {\"Refs.\": \"R. Lin, K. Xiao, Z. Qin, Q. Han, C. Zhang, M. Wei, M. I. Saidaminov, Y. Gao, J. Xu, M. Xiao, A. Li, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2019, 4, 864.\", \"PCE [%]\": \"24.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.81\", \"Eg,bottom [eV]\": \"1.27\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8Cs0.2Pb(I0.6Br0.4)3\", \"Voc [mV]\": \"1927.0\"}, {\"Refs.\": \"A. F. Palmstrom, G. E. Eperon, T. Leijtens, R. Prasanna, S. N. Habisreutinger, W. Nemeth, E. A. Gaulding, S. P. Dunfield, M. Reese, S. Nanayakkara, T. Moot, J. Werner, J. Liu, B. To, S. T. Christensen, M. D. McGehee, M. F. A. M. van Hest, J. M. Luther, J. J. Berry, D. T. Moore, Joule 2019, 3, 2193.\", \"PCE [%]\": \"23.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.75Cs0.25Sn0.5Pb0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.73\", \"Eg,bottom [eV]\": \"1.28\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"16.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.6Cs0.3DMA0.1PbI2.4Br0.6\", \"Voc [mV]\": \"1880.0\"}, {\"Refs.\": \"Q. Zeng, L. Liu, Z. Xiao, F. Liu, Y. Hua, Y. Yuan, L. Ding, Sci. Bull. 2019, 64, 885.\", \"PCE [%]\": \"15.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"PTB7-Th:COi8DFIC:PC71BM\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.91\", \"Eg,bottom [eV]\": \"1.25\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.4\", \"Jsc [mA cm\\u22122]\": \"12.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"CsPbI2Br\", \"Voc [mV]\": \"1710.0\"}, {\"Refs.\": \"P. Wang, W. Li, O. J. Sandberg, C. Guo, R. Sun, H. Wang, D. Li, H. Zhang, S. Cheng, D. Liu, J. Min, A. Armin, T. Wang, Nano Lett. 2021, 21, 7845.\", \"PCE [%]\": \"21.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"PM6:Y6-BO\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.91\", \"Eg,bottom [eV]\": \"1.38\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.9\", \"Jsc [mA cm\\u22122]\": \"13.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"CsPbI2Br\", \"Voc [mV]\": \"1960.0\"}, {\"Refs.\": \"Z. Li, S. Wu, J. Zhang, K. C. Lee, H. Lei, F. Lin, Z. Wang, Z. Zhu, A. K. Y. Jen, Adv. Energy Mater. 2020, 10, 2000361.\", \"PCE [%]\": \"15.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"PBDB-T:SN6IC-4F\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.83\", \"Eg,bottom [eV]\": \"1.4\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.0\", \"Jsc [mA cm\\u22122]\": \"11.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.1(FA0.6MA0.4)0.9Pb(I0.6Br0.4)3\", \"Voc [mV]\": \"1850.0\"}, {\"Refs.\": \"X. Chen, Z. Jia, Z. Chen, T. Jiang, L. Bai, F. Tao, J. Chen, X. Chen, T. Liu, X. Xu, C. Yang, W. Shen, W. E. I. Sha, H. Zhu, Y. Yang, Joule 2020, 4, 1594.\", \"PCE [%]\": \"19.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"PBDBT-2F:Y6:PC71BM\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"1.4\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.2\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8MA0.02Cs0.18PbI1.8Br1.2\", \"Voc [mV]\": \"1925.0\"}, {\"Refs.\": \"X. Chen, Z. Jia, Z. Chen, T. Jiang, L. Bai, F. Tao, J. Chen, X. Chen, T. Liu, X. Xu, C. Yang, W. Shen, W. E. I. Sha, H. Zhu, Y. Yang, Joule 2020, 4, 1594.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"PBDBT-2F:Y6:PC71BM\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"1.4\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.5\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8MA0.02Cs0.18PbI1.8Br1.2\", \"Voc [mV]\": \"1902.0\"}, {\"Refs.\": \"M. Hosseinnezhad, J. Electron. Mater. 2019, 48, 5403.\", \"PCE [%]\": \"10.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"(FAPbI3)0.85(MAPbBr3)0.15\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.93\", \"Eg,bottom [eV]\": \"1.59\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"12.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"N719\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"Z. Jia, S. Qin, L. Meng, Q. Ma, I. Angunawela, J. Zhang, X. Li, Y. He, W. Lai, N. Li, H. Ade, C. J. Brabec, Y. Li, Nat. Commun. 2021, 12, 178.\", \"PCE [%]\": \"16.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PTB7-Th:BTPV-4F:PC71BM\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.66\", \"Eg,bottom [eV]\": \"1.23\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.5\", \"Jsc [mA cm\\u22122]\": \"14.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PM6:m-DTC-2F\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1650.0\"}, {\"Refs.\": \"L. Meng, Y. Zhang, X. Wan, C. Li, X. Zhang, Y. Wang, X. Ke, Z. Xiao, L. Ding, R. Xia, H.-L. Yip, Y. Cao, Y. Chen, Science 2018, 361, 1094.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PTB7-Th:O6T-4F:PC71BM\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.72\", \"Eg,bottom [eV]\": \"1.24\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.3\", \"Jsc [mA cm\\u22122]\": \"14.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PBDB-T:F-M\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1640.0\"}, {\"Refs.\": \"X. Huang, B. Sun, Y. Li, C. Jiang, D. Fan, J. Fan, S. R. Forrest, Appl. Phys. Lett. 2020, 116, 153501.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PM6:SFT8-4F\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.64\", \"Eg,bottom [eV]\": \"1.31\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PCE-10:BT-CIC:BEIT-4F\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1660.0\"}, {\"Refs.\": \"G. Liu, J. Jia, K. Zhang, X. e. Jia, Q. Yin, W. Zhong, L. Li, F. Huang, Y. Cao, Adv. Energy Mater. 2019, 9, 1803657.\", \"PCE [%]\": \"15.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PTB7-Th:PCDTBT:IEICO-4F\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.65\", \"Eg,bottom [eV]\": \"1.32\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.0\", \"Jsc [mA cm\\u22122]\": \"13.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PBDB-T-2F:TfIF-4FIC\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1600.0\"}, {\"Refs.\": \"J. Wang, Z. Zheng, Y. Zu, Y. Wang, X. Liu, S. Zhang, M. Zhang, J. Hou, Adv. Mater. 2021, 33, 2102787.\", \"PCE [%]\": \"19.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PBDB-TF:ITCC\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.74\", \"Eg,bottom [eV]\": \"1.32\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.4\", \"Jsc [mA cm\\u22122]\": \"14.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PBDB-TF:BTP-eC11\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1910.0\"}, {\"Refs.\": \"J. Wang, Z. Zheng, Y. Zu, Y. Wang, X. Liu, S. Zhang, M. Zhang, J. Hou, Adv. Mater. 2021, 33, 2102787.\", \"PCE [%]\": \"19.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PBDB-TF:ITCC\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.74\", \"Eg,bottom [eV]\": \"1.32\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"14.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PBDB-TF:BTP-eC11\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1912.0\"}, {\"Refs.\": \"M. M. Tavakoli, H. Si, J. Kong, Energy Technol. 2021, 9, 2000751.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PM6:Y6\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.73\", \"Eg,bottom [eV]\": \"1.37\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"12.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PV2000:PCBM\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1610.0\"}, {\"Refs.\": \"X. Che, Y. Li, Y. Qu, S. R. Forrest, Nat. Energy 2018, 3, 422.\", \"PCE [%]\": \"15.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PCE-10:BTCIC\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.79\", \"Eg,bottom [eV]\": \"1.42\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.0\", \"Jsc [mA cm\\u22122]\": \"13.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"DTDCPB:C70\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1590.0\"}, {\"Refs.\": \"Y. Zhang, B. Kan, Y. Sun, Y. Wang, R. Xia, X. Ke, Y.-Q.-Q. Yi, C. Li, H.-L. Yip, X. Wan, Y. Cao, Y. Chen, Adv. Mater. 2018, 30, 1707508.\", \"PCE [%]\": \"14.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PTB7-Th: NOBDT\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.74\", \"Eg,bottom [eV]\": \"1.48\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"11.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"PBDB-T: F-M\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1710.0\"}, {\"Refs.\": \"J. Troughton, S. Neubert, N. Gasparini, D. R. Villalva, J. Bertrandie, A. Seitkhan, S. H. K. Paleti, A. Sharma, M. De Bastiani, E. Aydin, T. D. Anthopoulos, S. De Wolf, R. Schlatmann, D. Baran, Adv. Energy Mater. 2021, 11, 2100166.\", \"PCE [%]\": \"15.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PTB7-Th:IEICO-4F\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.78\", \"Eg,bottom [eV]\": \"1.33\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.0\", \"Jsc [mA cm\\u22122]\": \"13.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"a-Si\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1610.0\"}, {\"Refs.\": \"A. B. Nikolskaia, M. F. Vildanova, S. S. Kozlov, O. I. Shevaleevskiy, Semiconductors 2018, 52, 88.\", \"PCE [%]\": \"14.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"Si\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.84\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.0\", \"Jsc [mA cm\\u22122]\": \"40.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"N719\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"580.0\"}, {\"Refs.\": \"J. Kwon, M. J. Im, C. U. Kim, S. H. Won, S. B. Kang, S. H. Kang, I. T. Choi, H. K. Kim, I. H. Kim, J. H. Park, K. J. Choi, Energy Environ. Sci. 2016, 9, 3657.\", \"PCE [%]\": \"17.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"Si\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.67\", \"Eg,bottom [eV]\": \"1.24\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.3\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"SGT-021\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1360.0\"}, {\"Refs.\": \"S. H. Moon, S. J. Park, S. H. Kim, M. W. Lee, J. Han, J. Y. Kim, H. Kim, Y. J. Hwang, D.-K. Lee, B. K. Min, Sci. Rep. 2015, 5, 8970.\", \"PCE [%]\": \"13.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"CIGS\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"1.21\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.0\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"N719\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"W.-S. Jeong, J.-W. Lee, S. Jung, J. H. Yun, N.-G. Park, Sol. Energy Mater. Sol. Cells 2011, 95, 3419.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"CIGS\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.9\", \"Eg,bottom [eV]\": \"1.22\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.0\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"N719\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1435.0\"}, {\"Refs.\": \"P. Liska, K. R. Thampi, M. Gr\\u00e4tzel, D. Br\\u00e9maud, D. Rudmann, H. M. Upadhyaya, A. N. Tiwari, Appl. Phys. Lett. 2006, 88, 203103.\", \"PCE [%]\": \"15.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"CIGS\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"1.22\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.0\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"N719\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1450.0\"}, {\"Refs.\": \"T. Kinoshita, J. T. Dy, S. Uchida, T. Kubo, H. Segawa, Nat. Photonics 2013, 7, 535.\", \"PCE [%]\": \"11.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"DX1\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.98\", \"Eg,bottom [eV]\": \"1.4\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.7\", \"Jsc [mA cm\\u22122]\": \"12.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"N719\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1400.0\"}, {\"Refs.\": \"T. Yamaguchi, Y. Uchida, S. Agatsuma, H. Arakawa, Sol. Energy Mater. Sol. Cells 2009, 93, 733.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"N719\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.95\", \"Eg,bottom [eV]\": \"1.44\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.0\", \"Jsc [mA cm\\u22122]\": \"10.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"Black dye\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1450.0\"}, {\"Refs.\": \"A. K. Baranwal, T. Shiki, Y. Ogomi, S. S. Pandey, T. Ma, S. Hayase, RSC Adv. 2014, 4, 47735.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"N719\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"2.37\", \"Eg,bottom [eV]\": \"1.78\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.0\", \"Jsc [mA cm\\u22122]\": \"7.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table9\", \"Top absorber\": \"D131\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1420.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2020, 28, 629.\", \"PCE [%]\": \"32.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"GaAs\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.9\", \"Eg,bottom [eV]\": \"1.35\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"85.7\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table10\", \"Top absorber\": \"GaInP\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2500.0\"}, {\"Refs.\": \"M. A. Green, Y. Hishikawa, E. D. Dunlop, D. H. Levi, J. Hohl-Ebinger, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2018, 26, 3.\", \"PCE [%]\": \"32.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"GaAs\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.88\", \"Eg,bottom [eV]\": \"1.41\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"87.7\", \"Jsc [mA cm\\u22122]\": \"14.66\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table10\", \"Top absorber\": \"GaInP\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2568.0\"}, {\"Refs.\": \"T. S. Kim, H. J. Kim, D.-M. Geum, J.-H. Han, I. S. Kim, N. Hong, G. H. Ryu, J. Kang, W. J. Choi, K. J. Yu, ACS Appl. Mater. Interfaces 2021, 13, 13248.\", \"PCE [%]\": \"27.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"GaAs\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.92\", \"Eg,bottom [eV]\": \"1.41\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"88.0\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table10\", \"Top absorber\": \"GaInP\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2400.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2016, 24, 905.\", \"PCE [%]\": \"31.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"GaAs\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.85\", \"Eg,bottom [eV]\": \"1.42\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"87.7\", \"Jsc [mA cm\\u22122]\": \"14.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table10\", \"Top absorber\": \"GaInP\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2538.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2020, 28, 629.\", \"PCE [%]\": \"23.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"Si\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.9\", \"Eg,bottom [eV]\": \"1.17\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.7\", \"Jsc [mA cm\\u22122]\": \"17.34\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table10\", \"Top absorber\": \"GaAsP\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1732.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2014, 22, 701.\", \"PCE [%]\": \"11.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"nc-Si\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.93\", \"Eg,bottom [eV]\": \"1.36\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.5\", \"Jsc [mA cm\\u22122]\": \"12.27\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table10\", \"Top absorber\": \"a-Si\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1428.0\"}, {\"Refs.\": \"M. Ma, Q. Tang, H. Chen, B. He, P. Yang, Sol. Energy Mater. Sol. Cells 2017, 160, 67.\", \"PCE [%]\": \"3.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(5-AVA)y(MA)1\\u2212yPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.47\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"40.6\", \"Jsc [mA cm\\u22122]\": \"14.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"616.0\"}, {\"Refs.\": \"N. Ren, B. Chen, R. Li, P. Wang, S. Mazumdar, B. Shi, C. Zhu, Y. Zhao, X. Zhang, Sol. RRL 2021, 5, 2000795.\", \"PCE [%]\": \"20.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.87MA0.13PbI3\\u2212xClx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.9\", \"Jsc [mA cm\\u22122]\": \"24.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1123.0\"}, {\"Refs.\": \"D. Yang, R. Yang, K. Wang, C. Wu, X. Zhu, J. Feng, X. Ren, G. Fang, S. Priya, S. Liu, Nat. Commun. 2018, 9, 3239.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.95Cs0.05PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.5\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"J. H. Heo, D. H. Shin, D. H. Song, D. H. Kim, S. J. Lee, S. H. Im, J. Mater. Chem. A 2018, 6, 8251.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI3\\u2212xBrx\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.9\", \"Jsc [mA cm\\u22122]\": \"22.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"J. Chung, S. S. Shin, K. Hwang, G. Kim, K. W. Kim, D. S. Lee, W. Kim, B. S. Ma, Y.-K. Kim, T.-S. Kim, J. Seo, Energy Environ. Sci. 2020, 13, 4854.\", \"PCE [%]\": \"20.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.95(MAPbBr3)0.05\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.6\", \"Jsc [mA cm\\u22122]\": \"21.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1190.0\"}, {\"Refs.\": \"E. Cho, Y. Y. Kim, D. S. Ham, J. H. Lee, J.-S. Park, J. Seo, S.-J. Lee, Nano Energy 2021, 82, 105737.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.95(MAPbBr3)0.05\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.8\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1160.0\"}, {\"Refs.\": \"L. Yang, Q. Xiong, Y. Li, P. Gao, B. Xu, H. Lin, X. Li, T. Miyasaka, J. Mater. Chem. A 2021, 9, 1574.\", \"PCE [%]\": \"19.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05Rb0.05(FA0.83MA0.17)0.90Pb(I0.95Br0.05)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"23.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1109.0\"}, {\"Refs.\": \"J. Chung, S. S. Shin, K. Hwang, G. Kim, K. W. Kim, D. S. Lee, W. Kim, B. S. Ma, Y.-K. Kim, T.-S. Kim, J. Seo, Energy Environ. Sci. 2020, 13, 4854.\", \"PCE [%]\": \"19.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.95(MAPbBr3)0.05\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.3\", \"Jsc [mA cm\\u22122]\": \"21.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1192.0\"}, {\"Refs.\": \"K. Huang, Y. Peng, Y. Gao, J. Shi, H. Li, X. Mo, H. Huang, Y. Gao, L. Ding, J. Yang, Adv. Energy Mater. 2019, 9, 1901419.\", \"PCE [%]\": \"19.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.945MA0.025Cs0.03Pb(I0.975Br0.025)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.0\", \"Jsc [mA cm\\u22122]\": \"23.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"S. Zhang, H. Wang, X. Duan, L. Rao, C. Gong, B. Fan, Z. Xing, X. Meng, B. Xie, X. Hu, Adv. Funct. Mater. 2021, n/a, 2106495.\", \"PCE [%]\": \"19.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.08MA0.05FA0.87PbI2.88Br0.12\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"X. Hu, X. Meng, X. Yang, Z. Huang, Z. Xing, P. Li, L. Tan, M. Su, F. Li, Y. Chen, Y. Song, Sci. Bulletin 2021, 66, 527.\", \"PCE [%]\": \"19.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAMAPb(IBr)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"23.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"X. Dai, Y. Deng, C. H. Van Brackle, S. Chen, P. N. Rudd, X. Xiao, Y. Lin, B. Chen, J. Huang, Adv. Energy Mater. 2020, 10, 1903108.\", \"PCE [%]\": \"19.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\\u2013NH4Cl\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"22.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"X. Yu, Z. Li, X. Sun, C. Zhong, Z. Zhu, Z. a. Li, A. K. Y. Jen, Nano Energy 2021, 82, 105701.\", \"PCE [%]\": \"17.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FA0.92MA0.08)0.9Cs0.1Pb(I0.92Br0.08)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"21.42\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"Z. Wang, L. Zeng, C. Zhang, Y. Lu, S. Qiu, C. Wang, C. Liu, L. Pan, S. Wu, J. Hu, G. Liang, P. Fan, H.-J. Egelhaaf, C. J. Brabec, F. Guo, Y. Mai, Adv. Funct. Mater. 2020, 30, 2001240.\", \"PCE [%]\": \"19.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"21.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"J. Feng, X. Zhu, Z. Yang, X. Zhang, J. Niu, Z. Wang, S. Zuo, S. Priya, S. Liu, D. Yang, Adv. Mater. 2018, 30, 1801418.\", \"PCE [%]\": \"18.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\\u2013dimethylsulfide\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"22.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1103.0\"}, {\"Refs.\": \"C. Liu, J. Sun, X.-F. Jiang, L. Huang, Q. Lou, Y.-B. Cheng, S. Song, Z. Ge, Sci. China Chem. 2021, 64, 281.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.79MA0.16PbI2.49Br0.51\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"22.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"C. Liu, L. Zhang, X. Zhou, J. Gao, W. Chen, X. Wang, B. Xu, Adv. Funct. Mater. 2019, 29, 1807604.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.81MA0.14PbI2.55Br0.45\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.9\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1062.0\"}, {\"Refs.\": \"M. M. Tavakoli, P. Yadav, D. Prochowicz, R. Tavakoli, Sol. RRL 2021, 5, 2000552.\", \"PCE [%]\": \"18.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.3\", \"Jsc [mA cm\\u22122]\": \"22.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"B. Cao, L. Yang, S. Jiang, H. Lin, N. Wang, X. Li, J. Mater. Chem. A 2019, 7, 4960.\", \"PCE [%]\": \"19.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Rb0.01K0.04 (Cs0.05(FA0.83MA0.17)0.95)0.95Pb(I0.83Br0.17)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.2\", \"Jsc [mA cm\\u22122]\": \"21.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1135.0\"}, {\"Refs.\": \"Q. Dong, C. Zhu, M. Chen, C. Jiang, J. Guo, Y. Feng, Z. Dai, S. K. Yadavalli, M. Hu, X. Cao, Y. Li, Y. Huang, Z. Liu, Y. Shi, L. Wang, N. P. Padture, Y. Zhou, Nat. Commun. 2021, 12, 973.\", \"PCE [%]\": \"20.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.04(FA0.84MA0.16)0.96Pb(I0.84Br0.16)3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"22.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1150.0\"}, {\"Refs.\": \"D. Xin, S. Tie, X. Zheng, J. Zhu, W.-H. Zhang, J. Energy Chem. 2020, 46, 173.\", \"PCE [%]\": \"18.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.06FA0.79MA0.15PbI2.55Br0.45\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.1\", \"Jsc [mA cm\\u22122]\": \"22.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"M. Gao, X. Han, X. Zhan, P. Liu, Y. Shan, Y. Chen, J. Li, R. Zhang, S. Wang, Q. Zhang, Y. Zheng, L. Chen, Mater. Lett. 2019, 248, 16.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(FAPbI3)0.85(MAPbBr3)0.15\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.8\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.9\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"J. Xi, Z. Wu, K. Xi, H. Dong, B. Xia, T. Lei, F. Yuan, W. Wu, B. Jiao, X. Hou, Nano Energy 2016, 26, 438.\", \"PCE [%]\": \"7.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"(\\u03b1-FAPbI3)0.5(MAPbI2Br)0.5\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.7\", \"Jsc [mA cm\\u22122]\": \"10.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1090.0\"}, {\"Refs.\": \"J. W. Kim, D. Yuk, W. Lee, S. Rasool, J. Y. Kim, ECS J. Solid State Sci. Technol. 2021, 10, 065007.\", \"PCE [%]\": \"7.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:COi 8DFIC:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.27\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.2\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"708.0\"}, {\"Refs.\": \"K.-W. Seo, J. Lee, J. Jo, C. Cho, J.-Y. Lee, Adv. Mater. 2019, 31, 1902447.\", \"PCE [%]\": \"10.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:IEICO-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.2\", \"Jsc [mA cm\\u22122]\": \"24.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"T.-Y. Qu, L.-J. Zuo, J.-D. Chen, X. Shi, T. Zhang, L. Li, K.-C. Shen, H. Ren, S. Wang, F.-M. Xie, Y.-Q. Li, A. K. Y. Jen, J.-X. Tang, Adv. Opt. Mater. 2020, 8, 2000669.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:N3:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.7\", \"Jsc [mA cm\\u22122]\": \"25.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"Z. Wang, Y. Han, L. Yan, C. Gong, J. Kang, H. Zhang, X. Sun, L. Zhang, J. Lin, Q. Luo, C.-Q. Ma, Adv. Funct. Mater. 2021, 31, 2007276.\", \"PCE [%]\": \"14.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.2\", \"Jsc [mA cm\\u22122]\": \"23.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"837.0\"}, {\"Refs.\": \"F. Qin, L. Sun, H. Chen, Y. Liu, X. Lu, W. Wang, T. Liu, X. Dong, P. Jiang, Y. Jiang, L. Wang, Y. Zhou, Adv. Mater. 2021, n/a, 2103017.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:BTP-eC9:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.8\", \"Jsc [mA cm\\u22122]\": \"25.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"J. Wan, Y. Xia, J. Fang, Z. Zhang, B. Xu, J. Wang, L. Ai, W. Song, K. N. Hui, X. Fan, Y. Li, Nano-Micro Lett. 2021, 13, 44.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"25.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"X. Chen, G. Xu, G. Zeng, H. Gu, H. Chen, H. Xu, H. Yao, Y. Li, J. Hou, Y. Li, Adv. Mater. 2020, 32, 1908478.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"25.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"832.0\"}, {\"Refs.\": \"T. Yan, W. Song, J. Huang, R. Peng, L. Huang, Z. Ge, Adv. Mater. 2019, 31, 1902210.\", \"PCE [%]\": \"14.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"23.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"828.0\"}, {\"Refs.\": \"W. Song, Y. Liu, B. Fanady, Y. Han, L. Xie, Z. Chen, K. Yu, X. Peng, X. Zhang, Z. Ge, Nano Energy 2021, 86, 106044.\", \"PCE [%]\": \"15.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6:C6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.6\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"847.0\"}, {\"Refs.\": \"J. Wan, Y. Xia, J. Fang, Z. Zhang, B. Xu, J. Wang, L. Ai, W. Song, K. N. Hui, X. Fan, Y. Li, Nano-Micro Lett. 2021, 13, 44.\", \"PCE [%]\": \"16.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"25.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"J. W. Kim, D. Yuk, W. Lee, S. Rasool, J. Y. Kim, ECS J. Solid State Sci. Technol. 2021, 10, 065007.\", \"PCE [%]\": \"10.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.2\", \"Jsc [mA cm\\u22122]\": \"17.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"848.0\"}, {\"Refs.\": \"Y.-X. Zhang, J. Fang, W. Li, Y. Shen, J.-D. Chen, Y. Li, H. Gu, S. Pelivani, M. Zhang, Y. Li, J.-X. Tang, ACS Nano 2019, 13, 4686.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.3\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"X. Dong, P. Shi, L. Sun, J. Li, F. Qin, S. Xiong, T. Liu, X. Jiang, Y. Zhou, J. Mater. Chem. A 2019, 7, 1989.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.2\", \"Jsc [mA cm\\u22122]\": \"19.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:IT-4F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"826.0\"}, {\"Refs.\": \"G. Zeng, J. Zhang, X. Chen, H. Gu, Y. Li, Y. Li, Sci. China Chem. 2019, 62, 851.\", \"PCE [%]\": \"10.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.8\", \"Jsc [mA cm\\u22122]\": \"18.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"900.0\"}, {\"Refs.\": \"Y. Yang, J. Ou, X. Lv, C. Meng, Y. Mai, Sol. Energy 2019, 180, 57.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTB7-Th:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"16.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"L. Gao, Z.-G. Zhang, H. Bin, L. Xue, Y. Yang, C. Wang, F. Liu, T. P. Russell, Y. Li, Adv. Mater. 2016, 28, 8288.\", \"PCE [%]\": \"9.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"J51:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.7\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"T. Xu, C. Gong, S. Wang, H. Lian, W. Lan, G. L\\u00e9v\\u00eaque, B. Grandidier, J. Plain, R. Bachelot, B. Wei, F. Zhu, Sol. RRL 2020, 4, 1900522.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T:ITIC\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.6\", \"Jsc [mA cm\\u22122]\": \"13.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"C. Xie, X. Jiang, Q. Zhu, D. Wang, C. Xiao, C. Liu, W. Ma, Q. Chen, W. Li, Small Methods 2021, 5, 2100481.\", \"PCE [%]\": \"7.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"JP02\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.3\", \"Jsc [mA cm\\u22122]\": \"10.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"925.0\"}, {\"Refs.\": \"D. H. Shin, S. W. Seo, J. M. Kim, H. S. Lee, S.-H. Choi, J. Alloys Compd. 2018, 744, 1.\", \"PCE [%]\": \"3.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"P3HT:PCBM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.2\", \"Jsc [mA cm\\u22122]\": \"10.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"592.0\"}, {\"Refs.\": \"K. G. Baiju, B. Murali, R. Subba Rao, K. Jayanarayanan, D. Kumaresan, Chem. Eng. Process. 2020, 149, 107817.\", \"PCE [%]\": \"4.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"53.9\", \"Jsc [mA cm\\u22122]\": \"9.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\", \"PCE [%]\": \"4.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.0\", \"Jsc [mA cm\\u22122]\": \"10.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"T. Yamaguchi, N. Tobe, D. Matsumoto, T. Nagai, H. Arakawa, Sol. Energy Mater. Sol. Cells 2010, 94, 812.\", \"PCE [%]\": \"7.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.75\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.2\", \"Jsc [mA cm\\u22122]\": \"15.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"732.0\"}, {\"Refs.\": \"F. Huang, D. Chen, Q. Li, R. A. Caruso, Y.-B. Cheng, Appl. Phys. Lett. 2012, 100, 123102.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.78\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.5\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"725.0\"}, {\"Refs.\": \"Y. Wang, P. Cheng, C. Feng, H. Zhang, W. Zhao, Sol. Energy 2019, 180, 423.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"13.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"729.0\"}, {\"Refs.\": \"H. C. Weerasinghe, P. M. Sirimanne, G. P. Simon, Y.-B. Cheng, Prog. Photovoltaic: Res. Appl. 2012, 20, 321.\", \"PCE [%]\": \"6.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.0\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"732.0\"}, {\"Refs.\": \"H. Lee, J. Kim, D. Y. Kim, Y. Seo, Org. Electron. 2018, 52, 103.\", \"PCE [%]\": \"6.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.9\", \"Jsc [mA cm\\u22122]\": \"12.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"(JH-1)0.6(SQ2)0.4\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"754.0\"}, {\"Refs.\": \"H. C. Weerasinghe, P. M. Sirimanne, G. V. Franks, G. P. Simon, Y. B. Cheng, J. Photochem. Photobiol., A 2010, 213, 30.\", \"PCE [%]\": \"5.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"183.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.8\", \"Jsc [mA cm\\u22122]\": \"10.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"735.0\"}, {\"Refs.\": \"Y. Xiao, J. Wu, G. Yue, J. Lin, M. Huang, Z. Lan, Electrochim. Acta 2011, 56, 8545.\", \"PCE [%]\": \"6.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.0\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"D. Kishore Kumar, M.-H. Hsu, A. Ivaturi, B. Chen, N. Bennett, H. M. Upadhyaya, Flexible Printed Electron. 2019, 4, 015007.\", \"PCE [%]\": \"4.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.9\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.7\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"L. Song, Y. Guan, P. Du, Y. Yang, F. Ko, J. Xiong, Sol. Energy Mater. Sol. Cells 2016, 147, 134.\", \"PCE [%]\": \"4.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.2\", \"Jsc [mA cm\\u22122]\": \"10.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"H. C. Weerasinghe, G. V. Franks, J. D. Plessis, G. P. Simon, Y.-B. Cheng, J. Mater. Chem. 2010, 20, 9954.\", \"PCE [%]\": \"4.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.95\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.3\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"702.0\"}, {\"Refs.\": \"X. Zhang, W. Guo, C. Pan, J. Mater. Chem. A 2016, 4, 6569.\", \"PCE [%]\": \"6.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.99\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"53.4\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"660.0\"}, {\"Refs.\": \"J. H. Kim, S.-J. Yoo, D. Lee, J. W. Choi, S.-C. Han, T. I. Ryu, H. W. Lee, M. Shin, M. Song, Nano Res. 2021, 14, 2728.\", \"PCE [%]\": \"5.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.12\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.3\", \"Jsc [mA cm\\u22122]\": \"10.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"A. F. Palmstrom, G. E. Eperon, T. Leijtens, R. Prasanna, S. N. Habisreutinger, W. Nemeth, E. A. Gaulding, S. P. Dunfield, M. Reese, S. Nanayakkara, T. Moot, J. Werner, J. Liu, B. To, S. T. Christensen, M. D. McGehee, M. F. A. M. van Hest, J. M. Luther, J. J. Berry, D. T. Moore, Joule 2019, 3, 2193.\", \"PCE [%]\": \"21.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.75Cs0.25Sn0.5Pb0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.73\", \"Eg,bottom [eV]\": \"1.28\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.6Cs0.3DMA0.1PbI2.4Br0.6\", \"Voc [mV]\": \"1820.0\"}, {\"Refs.\": \"Z. Li, S. Wu, J. Zhang, K. C. Lee, H. Lei, F. Lin, Z. Wang, Z. Zhu, A. K. Y. Jen, Adv. Energy Mater. 2020, 10, 2000361.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"PBDB-T:SN6IC-4F\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"1.4\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.3\", \"Jsc [mA cm\\u22122]\": \"11.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.1(FA0.6MA0.4)0.9Pb(I0.6Br0.4)3\", \"Voc [mV]\": \"1800.0\"}, {\"Refs.\": \"B. M. Kayes, L. Zhang, R. Twist, I. Ding, G. S. Higashi, IEEE J. Photovoltaics 2014, 4, 729.\", \"PCE [%]\": \"30.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"GaAs\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.86\", \"Eg,bottom [eV]\": \"1.41\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.7\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"InGaP\", \"Voc [mV]\": \"2547.0\"}, {\"Refs.\": \"T. S. Kim, H. J. Kim, D.-M. Geum, J.-H. Han, I. S. Kim, N. Hong, G. H. Ryu, J. Kang, W. J. Choi, K. J. Yu, ACS Appl. Mater. Interfaces 2021, 13, 13248.\", \"PCE [%]\": \"27.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"GaAs\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.92\", \"Eg,bottom [eV]\": \"1.41\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"88.0\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"InGaP\", \"Voc [mV]\": \"2400.0\"}, {\"Refs.\": \"K.-J. Yang, S. Kim, S.-Y. Kim, D.-H. Son, J. Lee, Y.-I. Kim, S.-J. Sung, D.-H. Kim, T. Enkhbat, J. Kim, J. Kim, W. Jo, J.-K. Kang, Adv. Funct. Mater. 2021, n/a, 2102238.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"Cu2ZnSn(S,Se)4\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.16\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.8\", \"Jsc [mA cm\\u22122]\": \"33.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"539.0\"}, {\"Refs.\": \"K. Li, F. Li, C. Chen, P. Jiang, S. Lu, S. Wang, Y. Lu, G. Tu, J. Guo, L. Shui, Z. Liu, B. Song, J. Tang, Nano Energy 2021, 86, 106101.\", \"PCE [%]\": \"6.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"Sb2Se3\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.9\", \"Jsc [mA cm\\u22122]\": \"25.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"415.0\"}, {\"Refs.\": \"M. I. Khalil, R. Bernasconi, A. Lucotti, A. Le Donne, R. A. Mereu, S. Binetti, J. L. Hart, M. L. Taheri, L. Nobili, L. Magagnin, J. Appl. Electrochem. 2021, 51, 209.\", \"PCE [%]\": \"0.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"Cu2ZnSnS4\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"35.5\", \"Jsc [mA cm\\u22122]\": \"7.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"204.0\"}, {\"Refs.\": \"Q. Tang, H. Shen, H. Yao, K. Gao, Y. Jiang, Y. Li, Y. Liu, L. Zhang, Z. Ni, Q. Wei, Renewable Energy 2019, 133, 883.\", \"PCE [%]\": \"17.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"c-Si\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.14\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"36.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"656.0\"}, {\"Refs.\": \"I. Hwang, H.-D. Um, B.-S. Kim, M. Wober, K. Seo, Energy Environ. Sci. 2018, 11, 641.\", \"PCE [%]\": \"18.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"c-Si\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.17\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"39.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"608.0\"}, {\"Refs.\": \"S.-T. Kim, H.-J. Jeong, Y.-C. Kim, V. Bhatt, M. Kumar, J.-H. Yun, J.-H. Jang, Energy Rep. 2021, 7, 2255.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.17\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.4\", \"Jsc [mA cm\\u22122]\": \"35.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"580.0\"}, {\"Refs.\": \"A. Chiril\\u0103, P. Reinhard, F. Pianezzi, P. Bloesch, A. R. Uhl, C. Fella, L. Kranz, D. Keller, C. Gretener, H. Hagendorfer, D. Jaeger, R. Erni, S. Nishiwaki, S. Buecheler, A. N. Tiwari, Nat. Mater. 2013, 12, 1107.\", \"PCE [%]\": \"20.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.2\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"35.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"736.0\"}, {\"Refs.\": \"R. Kaczynski, J. Lee, J. V. Alsburg, B. Sang, U. Schoop, J. Britt, presented at 2017 IEEE 44th Photovoltaic Spec. Conf. (PVSC), Washington, DC, USA 25\\u201330 June 2017.\", \"PCE [%]\": \"18.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGS\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.22\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.4\", \"Jsc [mA cm\\u22122]\": \"35.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"K. Ruan, K. Ding, Y. Wang, S. Diao, Z. Shao, X. Zhang, J. Jie, J. Mater. Chem. A 2015, 3, 14370.\", \"PCE [%]\": \"8.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"c-Si\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"24.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"550.0\"}, {\"Refs.\": \"S. Moon, K. Kim, Y. Kim, J. Heo, J. Lee, Sci. Rep. 2016, 6, 30107.\", \"PCE [%]\": \"22.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"GaAs\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.4\", \"Jsc [mA cm\\u22122]\": \"27.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"980.0\"}, {\"Refs.\": \"H. P. Mahabaduge, W. L. Rance, J. M. Burst, M. O. Reese, D. M. Meysing, C. A. Wolden, J. Li, J. D. Beach, T. A. Gessert, W. K. Metzger, S. Garner, T. M. Barnes, Appl. Phys. Lett. 2015, 106, 133501.\", \"PCE [%]\": \"16.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.4\", \"Jsc [mA cm\\u22122]\": \"25.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"831.0\"}, {\"Refs.\": \"L. Kranz, C. Gretener, J. Perrenoud, R. Schmitt, F. Pianezzi, F. La Mattina, P. Bl\\u00f6sch, E. Cheah, A. Chiril\\u0103, C. M. Fella, H. Hagendorfer, T. J\\u00e4ger, S. Nishiwaki, A. R. Uhl, S. Buecheler, A. N. Tiwari, Nat. Commun. 2013, 4, 2306.\", \"PCE [%]\": \"11.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.49\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.9\", \"Jsc [mA cm\\u22122]\": \"22.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"821.0\"}, {\"Refs.\": \"T. S\\u00f6derstr\\u00f6m, F.-J. Haug, V. Terrazzoni-Daudrix, C. Ballif, J. Appl. Phys. 2008, 103, 114509.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"a-Si:H\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"888.0\"}, {\"Refs.\": \"C. Zhang, Y. Song, M. Wang, M. Yin, X. Zhu, L. Tian, H. Wang, X. Chen, Z. Fan, L. Lu, D. Li, Adv. Funct. Mater. 2017, 27, 1604720.\", \"PCE [%]\": \"8.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"a-Si:H\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.0\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"S.-H. Lim, H.-J. Seok, M.-J. Kwak, D.-H. Choi, S.-K. Kim, D.-H. Kim, H.-K. Kim, Nano Energy 2021, 82, 105703.\", \"PCE [%]\": \"15.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"3.0\", \"Absorber\": \"Cs0.175FA0.75MA0.075Pb\\u00a0(I0.875Br0.125)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.2\", \"Jsc [mA cm\\u22122]\": \"19.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\", \"PCE [%]\": \"12.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"3.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.5\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1017.0\"}, {\"Refs.\": \"Z. Ying, X. Yang, J. Zheng, Y. Zhu, J. Xiu, W. Chen, C. Shou, J. Sheng, Y. Zeng, B. Yan, H. Pan, J. Ye, Z. He, J. Mater. Chem. A 2021, 9, 12009.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"4.0\", \"Absorber\": \"CsFAMAPb(IBr)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"21.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1076.0\"}, {\"Refs.\": \"B. Chen, Y. Bai, Z. Yu, T. Li, X. Zheng, Q. Dong, L. Shen, M. Boccard, A. Gruverman, Z. Holman, J. Huang, Adv. Energy Mater. 2016, 6, 1601128.\", \"PCE [%]\": \"16.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.2\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"P. You, Z. Liu, Q. Tai, S. Liu, F. Yan, Adv. Mater. 2015, 27, 3632.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.3\", \"Jsc [mA cm\\u22122]\": \"19.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"C. W. Jang, J. M. Kim, S.-H. Choi, J. Alloys Compd. 2019, 775, 905.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.9\", \"Jsc [mA cm\\u22122]\": \"18.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"940.0\"}, {\"Refs.\": \"J. H. Heo, H. J. Han, M. Lee, M. Song, D. H. Kim, S. H. Im, Energy Environ. Sci. 2015, 8, 2922.\", \"PCE [%]\": \"15.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"6.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.4\", \"Jsc [mA cm\\u22122]\": \"19.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"7.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.5\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"988.0\"}, {\"Refs.\": \"D. Yang, X. Zhang, Y. Hou, K. Wang, T. Ye, J. Yoon, C. Wu, M. Sanghadasa, S. Liu, S. Priya, Nano Energy 2021, 84, 105934.\", \"PCE [%]\": \"19.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"8.0\", \"Absorber\": \"Cs0.05FA0.95PbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.5\", \"Jsc [mA cm\\u22122]\": \"21.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1137.0\"}, {\"Refs.\": \"S.-H. Lim, H.-J. Seok, M.-J. Kwak, D.-H. Choi, S.-K. Kim, D.-H. Kim, H.-K. Kim, Nano Energy 2021, 82, 105703.\", \"PCE [%]\": \"17.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"Cs0.175FA0.825Pb(I0.875Br0.125)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.1\", \"Jsc [mA cm\\u22122]\": \"21.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1083.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"17.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.1\", \"Jsc [mA cm\\u22122]\": \"22.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.5\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"12.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.8\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"14.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"13.0\", \"Absorber\": \"MAPbI2.5Br0.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.4\", \"Jsc [mA cm\\u22122]\": \"19.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1100.0\"}, {\"Refs.\": \"S.-H. Lim, H.-J. Seok, M.-J. Kwak, D.-H. Choi, S.-K. Kim, D.-H. Kim, H.-K. Kim, Nano Energy 2021, 82, 105703.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"Cs0.175FA0.825Pb(I0.875Br0.125)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.6\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1048.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"13.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.9\", \"Jsc [mA cm\\u22122]\": \"19.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"11.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"15.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.3\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"13.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"16.0\", \"Absorber\": \"MAPbI2Br\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.76\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.4\", \"Jsc [mA cm\\u22122]\": \"16.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"16.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1040.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"12.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"MAPbI2Br\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.7\", \"Jsc [mA cm\\u22122]\": \"15.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"C. Li, J. Sleppy, N. Dhasmana, M. Soliman, L. Tetard, J. Thomas, J. Mater. Chem. A 2016, 4, 11648.\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.5\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1017.0\"}, {\"Refs.\": \"E. Della Gaspera, Y. Peng, Q. Hou, L. Spiccia, U. Bach, J. J. Jasieniak, Y.-B. Cheng, Nano Energy 2015, 13, 249.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.3\", \"Jsc [mA cm\\u22122]\": \"13.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"941.0\"}, {\"Refs.\": \"Y.-W. Zhang, P.-P. Cheng, W.-Y. Tan, Y. Min, Appl. Surf. Sci. 2021, 537, 147908.\", \"PCE [%]\": \"11.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"MAPbI3+ BiPy\\u00a0\\u2212\\u00a0I\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.6\", \"Jsc [mA cm\\u22122]\": \"14.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"14.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.2\", \"Jsc [mA cm\\u22122]\": \"17.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1108.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"14.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"21.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.2\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1117.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"22.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.7\", \"Jsc [mA cm\\u22122]\": \"17.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1073.0\"}, {\"Refs.\": \"Y. Dou, Z. Liu, Z. Wu, Y. Liu, J. Li, C. Leng, D. Fang, G. Liang, J. Xiao, W. Li, X. Wei, F. Huang, Y.-B. Cheng, J. Zhong, Nano Energy 2020, 71, 104567.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"KxCs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.6\", \"Jsc [mA cm\\u22122]\": \"17.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1082.0\"}, {\"Refs.\": \"S. Xiao, H. Chen, F. Jiang, Y. Bai, Z. Zhu, T. Zhang, X. Zheng, G. Qian, C. Hu, Y. Zhou, Y. Qu, S. Yang, Adv. Mater. Interfaces 2016, 3, 1600484.\", \"PCE [%]\": \"11.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"15.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1040.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.4\", \"Jsc [mA cm\\u22122]\": \"17.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"9.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"24.0\", \"Absorber\": \"MAPbI1.5Br1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.6\", \"Jsc [mA cm\\u22122]\": \"13.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"C.-Y. Chang, K.-T. Lee, W.-K. Huang, H.-Y. Siao, Y.-C. Chang, Chem. Mater. 2015, 27, 5122.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.7\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"950.0\"}, {\"Refs.\": \"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"26.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"12.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"27.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.2\", \"Jsc [mA cm\\u22122]\": \"18.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"F. Guo, H. Azimi, Y. Hou, T. Przybilla, M. Hu, C. Bronnbauer, S. Langner, E. Spiecker, K. Forberich, C. J. Brabec, Nanoscale 2015, 7, 1642.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"964.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.2\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.9\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"J. C. Yu, J. Sun, N. Chandrasekaran, C. J. Dunn, A. S. R. Chesman, J. J. Jasieniak, Nano Energy 2020, 71, 104635.\", \"PCE [%]\": \"7.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"Cs0.05(FA0.85MA0.15)0.95Pb(I0.85Br0.15)3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.2\", \"Jsc [mA cm\\u22122]\": \"11.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1010.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"11.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"31.0\", \"Absorber\": \"MAPbI2.5Br0.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.69\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.4\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1050.0\"}, {\"Refs.\": \"C. Rold\\u00e1n-Carmona, O. Malinkiewicz, R. Betancur, G. Longo, C. Momblona, F. Jaramillo, L. Camacho, H. J. Bolink, Energy Environ. Sci. 2014, 7, 2968.\", \"PCE [%]\": \"7.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"33.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.5\", \"Jsc [mA cm\\u22122]\": \"13.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1037.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"11.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"34.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.6\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"990.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"36.0\", \"Absorber\": \"MAPbI2Br\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.5\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1080.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.1\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1010.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.6\", \"Jsc [mA cm\\u22122]\": \"11.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"J. W. Jung, C.-C. Chueh, A. K. Y. Jen, Adv. Energy Mater. 2015, 5, 1500486.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"38.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"13.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"L. Yuan, Z. Wang, R. Duan, P. Huang, K. Zhang, Q. Chen, N. K. Allam, Y. Zhou, B. Song, Y. Li, J. Mater. Chem. A 2018, 6, 19696.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"41.0\", \"Absorber\": \"MAPbI1.5Br1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.9\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.2\", \"Jsc [mA cm\\u22122]\": \"12.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"42.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.6\", \"Jsc [mA cm\\u22122]\": \"13.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"H.-C. Kwon, A. Kim, H. Lee, D. Lee, S. Jeong, J. Moon, Adv. Energy Mater. 2016, 6, 1601055.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"45.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"12.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"C. O. Ram\\u00edrez Quiroz, I. Levchuk, C. Bronnbauer, M. Salvador, K. Forberich, T. Heum\\u00fcller, Y. Hou, P. Schweizer, E. Spiecker, C. J. Brabec, J. Mater. Chem. A 2015, 3, 24071.\", \"PCE [%]\": \"3.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"46.0\", \"Absorber\": \"MAPbI3\\u2212xClx\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.4\", \"Jsc [mA cm\\u22122]\": \"5.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"S. Bag, M. F. Durstock, Nano Energy 2016, 30, 542.\", \"PCE [%]\": \"4.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"47.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"8.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"66.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"52.9\", \"Jsc [mA cm\\u22122]\": \"2.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1000.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"68.0\", \"Absorber\": \"FAPbBr2.43Cl0.57\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.0\", \"Jsc [mA cm\\u22122]\": \"6.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1550.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"72.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.3\", \"Jsc [mA cm\\u22122]\": \"2.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\", \"PCE [%]\": \"0.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"72.0\", \"Absorber\": \"MAPbCl3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"3.03\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"35.4\", \"Jsc [mA cm\\u22122]\": \"0.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"73.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.1\", \"Jsc [mA cm\\u22122]\": \"2.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"D. Liu, C. Yang, R. R. Lunt, Joule 2018, 2, 1827.\", \"PCE [%]\": \"0.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"73.0\", \"Absorber\": \"MAPbCl2.4Br0.6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.84\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"44.9\", \"Jsc [mA cm\\u22122]\": \"0.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1260.0\"}, {\"Refs.\": \"G. Liu, C. Wu, Z. Zhang, Z. Chen, L. Xiao, B. Qu, Sol. RRL 2020, 4, 2000056.\", \"PCE [%]\": \"1.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"74.0\", \"Absorber\": \"Cs2AgBiBr6\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.62\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.1\", \"Jsc [mA cm\\u22122]\": \"2.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"970.0\"}, {\"Refs.\": \"Y.-M. Sung, M.-Z. Li, D. Luo, Y.-D. Li, S. Biring, Y.-C. Huang, C.-K. Wang, S.-W. Liu, K.-T. Wong, Nano Energy 2021, 80, 105565.\", \"PCE [%]\": \"13.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"1.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.5\", \"Jsc [mA cm\\u22122]\": \"24.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\", \"PCE [%]\": \"7.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"2.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDTTT-C-T:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.3\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"Y.-M. Sung, M.-Z. Li, D. Luo, Y.-D. Li, S. Biring, Y.-C. Huang, C.-K. Wang, S.-W. Liu, K.-T. Wong, Nano Energy 2021, 80, 105565.\", \"PCE [%]\": \"12.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"3.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.5\", \"Jsc [mA cm\\u22122]\": \"24.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"800.0\"}, {\"Refs.\": \"C.-K. Wang, B.-H. Jiang, J.-H. Lu, M.-T. Cheng, R.-J. Jeng, Y.-W. Lu, C.-P. Chen, K.-T. Wong, ChemSusChem 2020, 13, 903.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"6.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM7/PTTtID-Cl/IT-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.47\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.4\", \"Jsc [mA cm\\u22122]\": \"19.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"870.0\"}, {\"Refs.\": \"Y.-M. Sung, M.-Z. Li, D. Luo, Y.-D. Li, S. Biring, Y.-C. Huang, C.-K. Wang, S.-W. Liu, K.-T. Wong, Nano Energy 2021, 80, 105565.\", \"PCE [%]\": \"7.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"8.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"DTDCPB:C70\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.73\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.6\", \"Jsc [mA cm\\u22122]\": \"12.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\", \"PCE [%]\": \"14.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"23.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"854.0\"}, {\"Refs.\": \"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"11.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDTTT-C-T:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.4\", \"Jsc [mA cm\\u22122]\": \"14.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\", \"PCE [%]\": \"13.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"13.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"853.0\"}, {\"Refs.\": \"X. Li, R. Xia, K. Yan, J. Ren, H.-L. Yip, C.-Z. Li, H. Chen, ACS Energy Lett. 2020, 5, 3115.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.8\", \"Jsc [mA cm\\u22122]\": \"21.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"W. Song, Y. Liu, B. Fanady, Y. Han, L. Xie, Z. Chen, K. Yu, X. Peng, X. Zhang, Z. Ge, Nano Energy 2021, 86, 106044.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6:C6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.8\", \"Jsc [mA cm\\u22122]\": \"19.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"844.0\"}, {\"Refs.\": \"T. Xiao, J. Wang, S. Yang, Y. Zhu, D. Li, Z. Wang, S. Feng, L. Bu, X. Zhan, G. Lu, J. Mater. Chem. A 2020, 8, 401.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"15.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FNIC1\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"18.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"772.0\"}, {\"Refs.\": \"S. Wageh, M. Ra\\u00efssi, T. Berthelot, A. A. Al-Ghamdi, A. M. Abusorrah, W. Boukhili, O. A. Al-Hartomy, Adv. Eng. Mater. 2021, 23, 2001305.\", \"PCE [%]\": \"2.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"16.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"P3HT-PCBM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.95\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"55.4\", \"Jsc [mA cm\\u22122]\": \"9.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"540.0\"}, {\"Refs.\": \"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\", \"PCE [%]\": \"12.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T-2F:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.2\", \"Jsc [mA cm\\u22122]\": \"21.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"W. Song, B. Fanady, R. Peng, L. Hong, L. Wu, W. Zhang, T. Yan, T. Wu, S. Chen, Z. Ge, Adv. Energy Mater. 2020, 10, 2000136.\", \"PCE [%]\": \"11.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T-2F:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.6\", \"Jsc [mA cm\\u22122]\": \"20.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"Z. Hu, Z. Wang, Q. An, F. Zhang, Sci. Bull. 2020, 65, 131.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.4\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"852.0\"}, {\"Refs.\": \"Y. Bai, C. Zhao, R. Shi, J. Wang, F. Wang, T. Hayat, A. Alsaedi, Z. a. Tan, Mater. Chem. Front. 2020, 4, 2072.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.0\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"817.0\"}, {\"Refs.\": \"L. Chang, L. Duan, M. Sheng, J. Yuan, H. Yi, Y. Zou, A. Uddin, Nanomaterials 2020, 10, 1759.\", \"PCE [%]\": \"13.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"21.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:N3\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.5\", \"Jsc [mA cm\\u22122]\": \"25.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FOIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.3\", \"Jsc [mA cm\\u22122]\": \"20.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"736.0\"}, {\"Refs.\": \"Y. Bai, C. Zhao, X. Chen, S. Zhang, S. Zhang, T. Hayat, A. Alsaedi, Z. a. Tan, J. Hou, Y. Li, J. Mater. Chem. A 2019, 7, 15887.\", \"PCE [%]\": \"12.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"26.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T-2F:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.4\", \"Jsc [mA cm\\u22122]\": \"21.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"825.0\"}, {\"Refs.\": \"L. Chang, L. Duan, M. Sheng, J. Yuan, H. Yi, Y. Zou, A. Uddin, Nanomaterials 2020, 10, 1759.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:N3\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.1\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"K.-S. Chen, J.-F. Salinas, H.-L. Yip, L. Huo, J. Hou, A. K. Y. Jen, Energy Environ. Sci. 2012, 5, 9551.\", \"PCE [%]\": \"5.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDTTT-C-T:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"61.9\", \"Jsc [mA cm\\u22122]\": \"11.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"L. Chang, L. Duan, M. Sheng, J. Yuan, H. Yi, Y. Zou, A. Uddin, Nanomaterials 2020, 10, 1759.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"29.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:N3\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.7\", \"Jsc [mA cm\\u22122]\": \"15.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"800.0\"}, {\"Refs.\": \"R. Xia, C. J. Brabec, H.-L. Yip, Y. Cao, Joule 2019, 3, 2241.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.7\", \"Jsc [mA cm\\u22122]\": \"21.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"718.0\"}, {\"Refs.\": \"M. Yao, T. Li, Y. Long, P. Shen, G. Wang, C. Li, J. Liu, W. Guo, Y. Wang, L. Shen, X. Zhan, Sci. Bull. 2020, 65, 217.\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"34.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FOIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.1\", \"Jsc [mA cm\\u22122]\": \"18.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"733.0\"}, {\"Refs.\": \"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\", \"PCE [%]\": \"8.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"36.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:BT-CIC:TT-FIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.9\", \"Jsc [mA cm\\u22122]\": \"18.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"36.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.5\", \"Jsc [mA cm\\u22122]\": \"11.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"6.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"10.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"S. Song, H. W. Cho, J. Jeong, Y. J. Yoon, S. Y. Park, S. Song, B. H. Woo, Y. C. Jun, B. Walker, J. Y. Kim, Sol. RRL 2020, 4, 2000201.\", \"PCE [%]\": \"5.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"38.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.2\", \"Jsc [mA cm\\u22122]\": \"12.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"700.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"4.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"39.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.9\", \"Jsc [mA cm\\u22122]\": \"8.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"D. Corzo, E. Bihar, E. B. Alexandre, D. Rosas-Villalva, D. Baran, Adv. Funct. Mater. 2021, 31, 2005763.\", \"PCE [%]\": \"9.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"42.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"53.2\", \"Jsc [mA cm\\u22122]\": \"26.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\", \"PCE [%]\": \"8.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"43.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.1\", \"Jsc [mA cm\\u22122]\": \"16.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"730.0\"}, {\"Refs.\": \"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\", \"PCE [%]\": \"8.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"44.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:BT-CIC:TT-FIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.6\", \"Jsc [mA cm\\u22122]\": \"16.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\", \"PCE [%]\": \"10.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"46.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.6\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"Y. Li, X. Guo, Z. Peng, B. Qu, H. Yan, H. Ade, M. Zhang, S. R. Forrest, Proc. Natl. Acad. Sci. U. S. A. 2020, 117, 21147.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"47.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:A078\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"14.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"730.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"2.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"47.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"4.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"Y. Li, C. Ji, Y. Qu, X. Huang, S. Hou, C.-Z. Li, L.-S. Liao, L. J. Guo, S. R. Forrest, Adv. Mater. 2019, 31, 1903173.\", \"PCE [%]\": \"7.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"49.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE-10:BT-CIC:TT-FIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.6\", \"Jsc [mA cm\\u22122]\": \"14.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"670.0\"}, {\"Refs.\": \"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\", \"PCE [%]\": \"8.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"50.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FOIC:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"16.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"746.0\"}, {\"Refs.\": \"Q. Liu, L. G. Gerling, F. Bernal-Texca, J. Toudert, T. Li, X. Zhan, J. Martorell, Adv. Energy Mater. 2020, 10, 1904196.\", \"PCE [%]\": \"7.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"51.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:FOIC:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.7\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"749.0\"}, {\"Refs.\": \"W. Jose da Silva, H. P. Kim, A. Rashid bin Mohd Yusoff, J. Jang, Nanoscale 2013, 5, 9324.\", \"PCE [%]\": \"1.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"53.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PSEHTT:ICBA\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.86\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"54.8\", \"Jsc [mA cm\\u22122]\": \"3.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"890.0\"}, {\"Refs.\": \"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\", \"PCE [%]\": \"5.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"53.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"DPP2T:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.5\", \"Jsc [mA cm\\u22122]\": \"10.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"N. Chaturvedi, N. Gasparini, D. Corzo, J. Bertrandie, N. Wehbe, J. Troughton, D. Baran, Adv. Funct. Mater. 2021, 31, 2009996.\", \"PCE [%]\": \"9.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"60.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.1\", \"Jsc [mA cm\\u22122]\": \"22.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"680.0\"}, {\"Refs.\": \"J. Lee, H. Cha, H. Yao, J. Hou, Y.-H. Suh, S. Jeong, K. Lee, J. R. Durrant, ACS Appl. Mater. Interfaces 2020, 12, 32764.\", \"PCE [%]\": \"3.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"60.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"DPP2T:IEICO-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.2\", \"Jsc [mA cm\\u22122]\": \"7.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"749.0\"}, {\"Refs.\": \"L. Zuo, X. Shi, W. Fu, A. K.-Y. Jen, Adv. Mater. 2019, 31, 1901683.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"62.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PTB7-Th:6TIC-4F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.0\", \"Jsc [mA cm\\u22122]\": \"12.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"690.0\"}, {\"Refs.\": \"C. Yang, M. Moemeni, M. Bates, W. Sheng, B. Borhan, R. R. Lunt, Adv. Opt. Mater. 2020, 8, 1901536.\", \"PCE [%]\": \"1.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"73.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"COi8DFIC\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.0\", \"Jsc [mA cm\\u22122]\": \"1.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"990.0\"}, {\"Refs.\": \"Y. Zhao, R. R. Lunt, Adv. Energy Mater. 2013, 3, 1143.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"84.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBMMA:PEMA:(TBA)2Mo6Cl14\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.0\", \"Jsc [mA cm\\u22122]\": \"1.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"520.0\"}, {\"Refs.\": \"Y. Zhao, G. A. Meek, B. G. Levine, R. R. Lunt, Adv. Opt. Mater. 2014, 2, 606.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"86.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"Cy7\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.0\", \"Jsc [mA cm\\u22122]\": \"1.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"500.0\"}, {\"Refs.\": \"C. L\\u00f3pez-L\\u00f3pez, S. Colodrero, H. M\\u00edguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\", \"PCE [%]\": \"5.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"1.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"53.7\", \"Jsc [mA cm\\u22122]\": \"12.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"C. L\\u00f3pez-L\\u00f3pez, S. Colodrero, H. M\\u00edguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\", \"PCE [%]\": \"4.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.0\", \"Jsc [mA cm\\u22122]\": \"10.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"780.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"4.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.0\", \"Jsc [mA cm\\u22122]\": \"9.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719+SDA\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"5.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.0\", \"Jsc [mA cm\\u22122]\": \"11.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"C. L\\u00f3pez-L\\u00f3pez, S. Colodrero, H. M\\u00edguez, Phys. Chem. Chem. Phys. 2014, 16, 663.\", \"PCE [%]\": \"4.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.1\", \"Jsc [mA cm\\u22122]\": \"11.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"765.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"13.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"14.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SGT-021\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"851.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"9.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"14.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.5\", \"Jsc [mA cm\\u22122]\": \"14.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SGT-021\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"9.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"15.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.2\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SGT-021\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"850.0\"}, {\"Refs.\": \"M. Aftabuzzaman, C. K. Kim, H. Zhou, H. K. Kim, Nanoscale 2020, 12, 1602.\", \"PCE [%]\": \"9.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.5\", \"Jsc [mA cm\\u22122]\": \"15.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SGT-021\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"855.0\"}, {\"Refs.\": \"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\", \"PCE [%]\": \"8.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.4\", \"Jsc [mA cm\\u22122]\": \"16.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719 (EtOH)\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"4.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.0\", \"Jsc [mA cm\\u22122]\": \"9.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719+SDA\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"3.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.01\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.0\", \"Jsc [mA cm\\u22122]\": \"8.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"24.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.0\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.3\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719 (EtOH)\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"794.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"2.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.0\", \"Jsc [mA cm\\u22122]\": \"5.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719+SDA\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"Q. Huaulm\\u00e9, V. M. Mwalukuku, D. Joly, J. Liotier, Y. Kervella, P. Maldivi, S. Narbey, F. Oswald, A. J. Riquelme, J. A. Anta, R. Demadrille, Nat. Energy 2020, 5, 468.\", \"PCE [%]\": \"3.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"27.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.8\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"NPI\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"521.0\"}, {\"Refs.\": \"D. Colonna, V. Capogna, A. Lembo, T. M. Brown, A. Reale, A. D. Carlo, Appl. Phys. Express 2012, 5, 022303.\", \"PCE [%]\": \"1.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"30.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.19\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"3.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\", \"PCE [%]\": \"6.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"31.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.9\", \"Jsc [mA cm\\u22122]\": \"13.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TPA-1 (EtOH)\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"698.0\"}, {\"Refs.\": \"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\", \"PCE [%]\": \"6.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"33.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.3\", \"Jsc [mA cm\\u22122]\": \"12.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TPA-2 (EtOH)\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"711.0\"}, {\"Refs.\": \"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\", \"PCE [%]\": \"6.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"36.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"54.7\", \"Jsc [mA cm\\u22122]\": \"14.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TPA-1 (EtOH)\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"766.0\"}, {\"Refs.\": \"D. A. Chalkias, C. Charalampopoulos, S. Aivali, A. K. Andreopoulou, A. Karavioti, E. Stathatos, Energies 2021, 14, 1159.\", \"PCE [%]\": \"3.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.5\", \"Jsc [mA cm\\u22122]\": \"8.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"Cz-2\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"648.0\"}, {\"Refs.\": \"D. A. Chalkias, C. Charalampopoulos, A. K. Andreopoulou, A. Karavioti, E. Stathatos, J. Power Sources 2021, 496, 229842.\", \"PCE [%]\": \"5.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"38.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.31\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"54.2\", \"Jsc [mA cm\\u22122]\": \"13.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TPA-2 (EtOH)\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"769.0\"}, {\"Refs.\": \"K. Kim, S. K. Nam, J. H. Moon, ACS Appl. Energy Mater. 2020, 3, 5277.\", \"PCE [%]\": \"7.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"43.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.95\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"15.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"PdTPBP/BPEA\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"W. Naim, V. Novelli, I. Nikolinakos, N. Barbero, I. Dzeba, F. Grifoni, Y. Ren, T. Alnasser, A. Velardo, R. Borrelli, S. Haacke, S. M. Zakeeruddin, M. Graetzel, C. Barolo, F. Sauvage, JACS Au 2021, 1, 409.\", \"PCE [%]\": \"3.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"69.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.6\", \"Jsc [mA cm\\u22122]\": \"11.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"VG20-C16\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"422.0\"}, {\"Refs.\": \"W. Naim, V. Novelli, I. Nikolinakos, N. Barbero, I. Dzeba, F. Grifoni, Y. Ren, T. Alnasser, A. Velardo, R. Borrelli, S. Haacke, S. M. Zakeeruddin, M. Graetzel, C. Barolo, F. Sauvage, JACS Au 2021, 1, 409.\", \"PCE [%]\": \"2.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"76.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.9\", \"Jsc [mA cm\\u22122]\": \"8.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"VG20-C16\", \"Table\": \"ver2_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"406.0\"}, {\"Refs.\": \"S. W. Leow, W. Li, J. M. R. Tan, S. Venkataraj, V. Tunuguntla, M. Zhang, S. Magdassi, L. H. Wong, Sol. RRL 2021, n/a, 2100131.\", \"PCE [%]\": \"3.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"1.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"Cu2ZnSn(S,Se)4\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"42.8\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table20\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"475.0\"}, {\"Refs.\": \"S.-J. Lee, S.-J. Sung, K.-J. Yang, J.-K. Kang, J. Y. Kim, Y. S. Do, D.-H. Kim, ACS Appl. Energy Mater. 2020, 3, 12644.\", \"PCE [%]\": \"3.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"8.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"Sb2S3\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"42.0\", \"Jsc [mA cm\\u22122]\": \"12.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table20\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"679.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"2.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.9\", \"Jsc [mA cm\\u22122]\": \"23.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\", \"PCE [%]\": \"9.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.26\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.6\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"J. Kim, J. W. Lim, G. Kim, M. Shin, ACS Appl. Mater. Interfaces 2021, 13, 4968.\", \"PCE [%]\": \"6.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"7.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.92\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.7\", \"Jsc [mA cm\\u22122]\": \"11.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"881.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"9.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"K. Kim, W. N. Shafarman, Nano Energy 2016, 30, 488.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"46.5\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"597.0\"}, {\"Refs.\": \"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\", \"PCE [%]\": \"8.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"11.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.3\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"620.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"16.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.3\", \"Jsc [mA cm\\u22122]\": \"14.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.3\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-SiGe:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.3\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"M. Saifullah, S. Ahn, J. Gwak, S. Ahn, K. Kim, J. Cho, J. H. Park, Y. J. Eo, A. Cho, J.-S. Yoo, J. H. Yun, J. Mater. Chem. A 2016, 4, 10542.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.4\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.6\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.7\", \"Jsc [mA cm\\u22122]\": \"16.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.5\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"580.0\"}, {\"Refs.\": \"S. H. Moon, S. J. Park, Y. J. Hwang, D.-K. Lee, Y. Cho, D.-W. Kim, B. K. Min, Sci. Rep. 2014, 4, 4408.\", \"PCE [%]\": \"1.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"40.8\", \"Jsc [mA cm\\u22122]\": \"8.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"495.0\"}, {\"Refs.\": \"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\", \"PCE [%]\": \"5.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"22.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.6\", \"Jsc [mA cm\\u22122]\": \"12.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"6.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.92\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"10.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"J. Wook Lim, M. Shin, D. J. Lee, S. Hyun Lee, S. Jin Yun, Sol. Energy Mater. Sol. Cells 2014, 128, 301.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"24.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.3\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"A. Mutalikdesai, S. K. Ramasesha, Thin Solid Films 2017, 632, 73.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CdTe\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"27.2\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"101.0\"}, {\"Refs.\": \"S. Kim, J. Yi, J. Kim, Sol. RRL 2021, n/a, 2100162.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"41.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.17\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"47.3\", \"Jsc [mA cm\\u22122]\": \"3.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"596.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"2.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.9\", \"Jsc [mA cm\\u22122]\": \"23.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\", \"PCE [%]\": \"9.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.26\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.6\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"J. Kim, J. W. Lim, G. Kim, M. Shin, ACS Appl. Mater. Interfaces 2021, 13, 4968.\", \"PCE [%]\": \"6.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"7.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.92\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.7\", \"Jsc [mA cm\\u22122]\": \"11.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"881.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"9.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"20.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"630.0\"}, {\"Refs.\": \"K. Kim, W. N. Shafarman, Nano Energy 2016, 30, 488.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"46.5\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"597.0\"}, {\"Refs.\": \"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\", \"PCE [%]\": \"8.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"11.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.3\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"620.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"16.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.3\", \"Jsc [mA cm\\u22122]\": \"14.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"17.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.3\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"810.0\"}, {\"Refs.\": \"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-SiGe:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.3\", \"Jsc [mA cm\\u22122]\": \"14.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"M. Saifullah, S. Ahn, J. Gwak, S. Ahn, K. Kim, J. Cho, J. H. Park, Y. J. Eo, A. Cho, J.-S. Yoo, J. H. Yun, J. Mater. Chem. A 2016, 4, 10542.\", \"PCE [%]\": \"5.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"18.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"57.4\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"7.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.87\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.6\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"M. J. Shin, S. Park, A. Lee, S. J. Park, A. Cho, K. Kim, S. K. Ahn, J. Hyung Park, J. Yoo, D. Shin, I. Jeong, J. H. Yun, J. Gwak, J.-S. Cho, Appl. Surf. Sci. 2021, 535, 147732.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.3\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.7\", \"Jsc [mA cm\\u22122]\": \"16.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"M. J. Shin, J. H. Jo, A. Cho, J. Gwak, J. H. Yun, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, I. Jeong, B.-H. Choi, J.-S. Cho, Sol. Energy 2019, 181, 276.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.5\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"580.0\"}, {\"Refs.\": \"S. H. Moon, S. J. Park, Y. J. Hwang, D.-K. Lee, Y. Cho, D.-W. Kim, B. K. Min, Sci. Rep. 2014, 4, 4408.\", \"PCE [%]\": \"1.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CIGS\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"40.8\", \"Jsc [mA cm\\u22122]\": \"8.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"495.0\"}, {\"Refs.\": \"J. W. Lim, S. H. Lee, D. J. Lee, Y. J. Lee, S. J. Yun, Thin Solid Films 2013, 547, 212.\", \"PCE [%]\": \"5.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"22.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.05\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"58.6\", \"Jsc [mA cm\\u22122]\": \"12.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"J.-S. Cho, Y. H. Seo, B.-H. Choi, A. Cho, A. Lee, M. J. Shin, K. Kim, S. K. Ahn, J. H. Park, J. Yoo, D. Shin, I. Jeong, J. Gwak, Sol. Energy Mater. Sol. Cells 2019, 202, 110078.\", \"PCE [%]\": \"6.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.92\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"10.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"J. Wook Lim, M. Shin, D. J. Lee, S. Hyun Lee, S. Jin Yun, Sol. Energy Mater. Sol. Cells 2014, 128, 301.\", \"PCE [%]\": \"6.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"24.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.68\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.3\", \"Jsc [mA cm\\u22122]\": \"10.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"A. Mutalikdesai, S. K. Ramasesha, Thin Solid Films 2017, 632, 73.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"37.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"CdTe\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"27.2\", \"Jsc [mA cm\\u22122]\": \"14.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"101.0\"}, {\"Refs.\": \"S. Kim, J. Yi, J. Kim, Sol. RRL 2021, n/a, 2100162.\", \"PCE [%]\": \"1.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"41.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"a-Si:H\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.17\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"47.3\", \"Jsc [mA cm\\u22122]\": \"3.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table21\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"596.0\"}, {\"Refs.\": \"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"7.8\", \"200 h PCE [%]\": \"7.2\", \"100 h PCE [%]\": \"6.8\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:ITIC-2F\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, N2, 40\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.5\", \"E1000h [Wh cm\\u22122]\": \"7.0\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"C. Xie, T. Heum\\u00fcller, W. Gruber, X. Tang, A. Classen, I. Schuldes, M. Bidwell, A. Sp\\u00e4th, R. H. Fink, T. Unruh, I. McCulloch, N. Li, C. J. Brabec, Nat. Commun. 2018, 9, 5335.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"5.0\", \"200 h PCE [%]\": \"5.0\", \"100 h PCE [%]\": \"4.7\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"P3HT:o-IDTBR\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, N2, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.0\", \"E1000h [Wh cm\\u22122]\": \"4.8\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"['A. Aubele, Y. He, T. Kraus, N. Li, E. Mena-Osteritz, P. Weitz, T. Heum\\u00fcller, K. Zhang, C. J. Brabec, P. B\\u00e4uerle, Adv. Mater. 2021, n/a, 2103573.', 'Additional Supporting Information: Molecular Oligothiophene\\u2013Fullerene Dyad Reaching Over 5% Efficiency in Single-Material Organic Solar Cells, https://emerging-pv.org/wp-content/uploads/2021/09/ASI_stability-OPV_10.1002adma.202103573.pdf (accessed: September 2021).']\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"5.1\", \"200 h PCE [%]\": \"4.9\", \"100 h PCE [%]\": \"4.9\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"Dyad 4\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, N2, 30\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.1\", \"E1000h [Wh cm\\u22122]\": \"4.9\", \"Eg [eV]\": \"1.61\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.0\", \"200 h PCE [%]\": \"7.4\", \"100 h PCE [%]\": \"7.0\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:ITIC-Th\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, N2, 40\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.5\", \"E1000h [Wh cm\\u22122]\": \"7.3\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"A. Classen, T. Heumueller, I. Wabra, J. Gerner, Y. He, L. Einsiedler, N. Li, G. J. Matt, A. Osvet, X. Du, A. Hirsch, C. J. Brabec, Adv. Energy Mater. 2019, 9, 1902124.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.7\", \"200 h PCE [%]\": \"8.1\", \"100 h PCE [%]\": \" \", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:IDTBR\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, N2, 35\\u201340\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.6\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"X. Du, T. Heumueller, W. Gruber, A. Classen, T. Unruh, N. Li, C. J. Brabec, Joule 2019, 3, 215.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"5.9\", \"200 h PCE [%]\": \"5.6\", \"100 h PCE [%]\": \"5.4\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-T:PCBM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, N2, 40\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.1\", \"E1000h [Wh cm\\u22122]\": \"5.6\", \"Eg [eV]\": \"1.84\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"M. Ra\\u00efssi, S. Leroy-Lhez, B. Ratier, Org. Electron. 2016, 37, 183.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"3.7\", \"200 h PCE [%]\": \"3.7\", \"100 h PCE [%]\": \"3.7\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"P3HT-PCBM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, air\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"0.7\", \"E1000h [Wh cm\\u22122]\": \"3.7\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"9.0\", \"200 h PCE [%]\": \"9.0\", \"100 h PCE [%]\": \"8.2\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 65\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.8\", \"E1000h [Wh cm\\u22122]\": \"8.7\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TF-tBu_C3F7\", \"Table\": \"ver2_table24\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"S. G. Hashmi, M. \\u00d6zkan, J. Halme, S. M. Zakeeruddin, J. Paltakari, M. Gr\\u00e4tzel, P. D. Lund, Energy Environ. Sci. 2016, 9, 2453.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"6.5\", \"200 h PCE [%]\": \"6.7\", \"100 h PCE [%]\": \"6.3\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 35\\u00a0\\u00b0C, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.4\", \"E1000h [Wh cm\\u22122]\": \"6.6\", \"Eg [eV]\": \"1.75\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table24\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"R. Jiang, A. Anderson, P. R. F. Barnes, L. Xiaoe, C. Law, B. C. O'Regan, J. Mater. Chem. A 2014, 2, 4751.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"6.3\", \"200 h PCE [%]\": \"5.8\", \"100 h PCE [%]\": \"4.8\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED, 20\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.3\", \"E1000h [Wh cm\\u22122]\": \"5.5\", \"Eg [eV]\": \"1.77\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"Z907\", \"Table\": \"ver2_table24\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"S. M. Seo, C. K. Kim, H. K. Kim, J. Mater. Chem. A 2019, 7, 14743.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"9.3\", \"200 h PCE [%]\": \"9.9\", \"100 h PCE [%]\": \"7.9\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 50\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.9\", \"E1000h [Wh cm\\u22122]\": \"9.2\", \"Eg [eV]\": \"1.78\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table24\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"W. Xiang, W. Huang, U. Bach, L. Spiccia, Chem. Commun. 2013, 49, 8997.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.4\", \"200 h PCE [%]\": \"8.3\", \"100 h PCE [%]\": \" \", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, w-LED\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.7\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"MK2\", \"Table\": \"ver2_table24\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"J. Xia, Q. Wang, M. Chen, W. Li, J. Liu, J. Chen, H. Wu, S. Fan, Electrochim. Acta 2019, 307, 422.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"8.0\", \"200 h PCE [%]\": \"8.3\", \"100 h PCE [%]\": \"8.3\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.4\", \"E1000h [Wh cm\\u22122]\": \"8.1\", \"Eg [eV]\": \"1.85\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver2_table24\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"J. Gao, M. Bhagavathi Achari, L. Kloo, Chem. Commun. 2014, 50, 6249.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"5.8\", \"200 h PCE [%]\": \"6.5\", \"100 h PCE [%]\": \"5.9\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"OC, AM1.5G, 60\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.3\", \"E1000h [Wh cm\\u22122]\": \"6.2\", \"Eg [eV]\": \"2.07\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"D35\", \"Table\": \"ver2_table24\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"K. Xiao, R. Lin, Q. Han, Y. Hou, Z. Qin, H. T. Nguyen, J. Wen, M. Wei, V. Yeddu, M. I. Saidaminov, Y. Gao, X. Luo, Y. Wang, H. Gao, C. Zhang, J. Xu, J. Zhu, E. H. Sargent, H. Tan, Nat. Energy 2020, 5, 870.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"24.4\", \"200 h PCE [%]\": \"24.3\", \"100 h PCE [%]\": \"19.3\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"1.26\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FSA:MA0.3FA0.7Pb0.5Sn0.5I3\", \"Comments\": \"MPP, encapsulation, air, 30\\u201350% RH, AM1.5G, no UV-f, 54\\u201360\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.9\", \"E1000h [Wh cm\\u22122]\": \"21.8\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table25\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8Cs0.2Pb(I0.6Br0.4)3\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"Z. Yu, Z. Yang, Z. Ni, Y. Shao, B. Chen, Y. Lin, H. Wei, Z. J. Yu, Z. Holman, J. Huang, Nat. Energy 2020, 5, 657.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"21.2\", \"200 h PCE [%]\": \"20.6\", \"100 h PCE [%]\": \"19.8\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"1.26\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Cs0.05MA0.45FA0.5Pb0.5Sn0.5I3\", \"Comments\": \"MPP-RL, encapsulation, air, AM1.5G, room T\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.2\", \"E1000h [Wh cm\\u22122]\": \"20.7\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.82\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table25\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.4FA0.6PbI1.95Br1.05\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"J. Tong, Z. Song, D. H. Kim, X. Chen, C. Chen, A. F. Palmstrom, P. F. Ndione, M. O. Reese, S. P. Dunfield, O. G. Reid, J. Liu, F. Zhang, S. P. Harvey, Z. Li, S. T. Christensen, G. Teeter, D. Zhao, M. M. Al-Jassim, M. F. A. M. van Hest, M. C. Beard, S. E. Shaheen, J. J. Berry, Y. Yan, K. Zhu, Science 2019, 364, 475.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"23.1\", \"200 h PCE [%]\": \"22.2\", \"100 h PCE [%]\": \"20.4\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"1.27\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"(FASnI3)0.6(MAPbI3)0.4\", \"Comments\": \"MPP, AM1.5G\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.7\", \"E1000h [Wh cm\\u22122]\": \"21.4\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.72\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table25\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.05FA0.8MA0.15PbI2.55Br0.45\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"Z. Li, T. H. Kim, S. Y. Han, Y.-J. Yun, S. Jeong, B. Jo, S. A. Ok, W. Yim, S. H. Lee, K. Kim, S. Moon, J.-Y. Park, T. K. Ahn, H. Shin, J. Lee, H. J. Park, Adv. Energy Mater. 2020, 10, 1903085.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"24.1\", \"200 h PCE [%]\": \"23.9\", \"100 h PCE [%]\": \"22.1\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"1.42\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"GaAs\", \"Comments\": \"MPP, air 20\\u201325% RH, AM1.5G, room T, UV-f\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.76\", \"E1000h [Wh cm\\u22122]\": \"23.3\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.85\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table25\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.80MA0.04Cs0.16Pb(I0.50Br0.50)3\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"Q. Han, Y.-T. Hsieh, L. Meng, J.-L. Wu, P. Sun, E.-P. Yao, S.-Y. Chang, S.-H. Bae, T. Kato, V. Bermudez, Y. Yang, Science 2018, 361, 904.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"22.0\", \"200 h PCE [%]\": \"19.9\", \"100 h PCE [%]\": \"18.4\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"1.1\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CIGS\", \"Comments\": \"MPP, air 20% RH, 30\\u00a0\\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.1\", \"E1000h [Wh cm\\u22122]\": \"19.4\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.65\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver2_table25\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.09FA0.77MA0.14Pb(I0.86Br0.14)3\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"Y. Lei, Y. Li, C. Lu, Q. Yan, Y. Wu, F. Babbe, H. Gong, S. Zhang, J. Zhou, R. Wang, R. Zhang, Y. Chen, H. Tsai, Y. Gu, H. Hu, Y.-H. Lo, W. Nie, T. Lee, J. Luo, K. Yang, K.-I. Jang, S. Xu, Nature 2022, 608, 317.\", \"PCE [%]\": \"12.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPb0.5Sn0.5Br3:Bi3+:BA2MA4Sn5I16\\u00a0\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.12\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.9\", \"Jsc [mA cm\\u22122]\": \"17.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"967.0\"}, {\"Refs.\": \"X. Zhou, L. Zhang, J. Yu, D. Wang, C. Liu, S. Chen, Y. Li, Y. Li, M. Zhang, Y. Peng, Y. Tian, J. Huang, X. Wang, X. Guo, B. Xu, Adv. Mater. 2022, 34, 2205809.\", \"PCE [%]\": \"24.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.7MA0.3Pb0.7Sn0.3I3/BTBTI:PCBM\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.18\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"29.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"X. Zhou, L. Zhang, J. Yu, D. Wang, C. Liu, S. Chen, Y. Li, Y. Li, M. Zhang, Y. Peng, Y. Tian, J. Huang, X. Wang, X. Guo, B. Xu, Adv. Mater. 2022, 34, 2205809.\", \"PCE [%]\": \"23.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.7MA0.3Pb0.7Sn0.3I3/BTBTI:PCBM\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.18\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.8\", \"Jsc [mA cm\\u22122]\": \"28.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1067.0\"}, {\"Refs.\": \"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\", \"PCE [%]\": \"22.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.25\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"33.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"841.0\"}, {\"Refs.\": \"G. Kapil, T. Bessho, Y. Sanehira, S. R. Sahamir, M. Chen, A. K. Baranwal, D. Liu, Y. Sono, D. Hirotani, D. Nomura, K. Nishimura, M. A. Kamarudin, Q. Shen, H. Segawa, S. Hayase, ACS Energy Lett. 2022, 7, 966.\", \"PCE [%]\": \"23.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.025FA0.475MA0.5Pb0.5Sn0.5I2.925Br0.075\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.29\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.8\", \"Jsc [mA cm\\u22122]\": \"32.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"J. Sanchez-Diaz, R. S. S\\u00e1nchez, S. Masi, M. Kre\\u0109marov\\u00e1, A. O. Alvarez, E. M. Barea, J. Rodriguez-Romero, V. S. Chirvony, J. F. S\\u00e1nchez-Royo, J. P. Martinez-Pastor, I. Mora-Ser\\u00f3, Joule 2022, 6, 861.\", \"PCE [%]\": \"10.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASnI3\\u00a0+ DipI + NaBH4\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.6\", \"Jsc [mA cm\\u22122]\": \"22.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"655.0\"}, {\"Refs.\": \"Z. Zhu, X. Jiang, D. Yu, N. Yu, Z. Ning, Q. Mi, ACS Energy Lett. 2022, 7, 2079.\", \"PCE [%]\": \"14.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.2\", \"Jsc [mA cm\\u22122]\": \"20.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"920.0\"}, {\"Refs.\": \"Y. Su, J. Yang, G. Liu, W. Sheng, J. Zhang, Y. Zhong, L. Tan, Y. Chen, Adv. Funct. Mater. 2022, 32, 2109631.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"EA0.098EDA0.01FA0.882SnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.3\", \"Jsc [mA cm\\u22122]\": \"21.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"750.0\"}, {\"Refs.\": \"T. Wu, X. Liu, X. Luo, H. Segawa, G. Tong, Y. Zhang, L. K. Ono, Y. Qi, L. Han, Nano-Micro Lett. 2022, 14, 99.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FASnI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.8\", \"Jsc [mA cm\\u22122]\": \"22.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"840.0\"}, {\"Refs.\": \"Q. Jiang, J. Tong, Y. Xian, R. A. Kerner, S. P. Dunfield, C. Xiao, R. A. Scheidt, D. Kuciauskas, X. Wang, M. P. Hautzinger, R. Tirawat, M. C. Beard, D. P. Fenning, J. J. Berry, B. W. Larson, Y. Yan, K. Zhu, Nature 2022, 611, 278.\", \"PCE [%]\": \"25.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.85MA0.05Rb0.05PbBr0.15I2.85\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.9\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1150.0\"}, {\"Refs.\": \"Q. Jiang, J. Tong, Y. Xian, R. A. Kerner, S. P. Dunfield, C. Xiao, R. A. Scheidt, D. Kuciauskas, X. Wang, M. P. Hautzinger, R. Tirawat, M. C. Beard, D. P. Fenning, J. J. Berry, B. W. Larson, Y. Yan, K. Zhu, Nature 2022, 611, 278.\", \"PCE [%]\": \"24.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.85MA0.05Rb0.05PbBr0.15I2.85\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.4\", \"Jsc [mA cm\\u22122]\": \"25.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1161.0\"}, {\"Refs.\": \"Z. Xiong, X. Chen, B. Zhang, G. O. Odunmbaku, Z. Ou, B. Guo, K. Yang, Z. Kan, S. Lu, S. Chen, N. A. N. Ouedraogo, Y. Cho, C. Yang, J. Chen, K. Sun, Adv. Mater. 2022, 34, 2106118.\", \"PCE [%]\": \"24.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAxMA1-xPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.7\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1180.0\"}, {\"Refs.\": \"F. Zhang, Y. Park So, C. Yao, H. Lu, P. Dunfield Sean, C. Xiao, S. Uli\\u010dn\\u00e1, X. Zhao, L. Du Hill, X. Chen, X. Wang, E. Mundt Laura, H. Stone Kevin, T. Schelhas Laura, G. Teeter, S. Parkin, L. Ratcliff Erin, Y.-L. Loo, J. Berry Joseph, C. Beard Matthew, Y. Yan, W. Larson Bryon, K. Zhu, Science 2022, 375, 71.\", \"PCE [%]\": \"24.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.97MA0.03PbI2.91Br0.09\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.8\", \"Jsc [mA cm\\u22122]\": \"25.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1158.0\"}, {\"Refs.\": \"M. Kim, J. Jeong, H. Lu, K. Lee Tae, T. Eickemeyer Felix, Y. Liu, W. Choi In, J. Choi Seung, Y. Jo, H.-B. Kim, S.-I. Mo, Y.-K. Kim, H. Lee, G. An Na, S. Cho, R. Tress Wolfgang, M. Zakeeruddin Shaik, A. Hagfeldt, Y. Kim Jin, M. Gr\\u00e4tzel, S. Kim Dong, Science 2022, 375, 302.\", \"PCE [%]\": \"25.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.9\", \"Jsc [mA cm\\u22122]\": \"26.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1174.0\"}, {\"Refs.\": \"Y. Zhao, F. Ma, Z. Qu, S. Yu, T. Shen, H.-X. Deng, X. Chu, X. Peng, Y. Yuan, X. Zhang, J. You, Science 2022, 377, 531.\", \"PCE [%]\": \"25.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbI3: (PbI2)2RbCl\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.6\", \"Jsc [mA cm\\u22122]\": \"26.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1182.0\"}, {\"Refs.\": \"Y. Li, Z. Chen, B. Yu, S. Tan, Y. Cui, H. Wu, Y. Luo, J. Shi, D. Li, Q. Meng, Joule 2022, 6, 676.\", \"PCE [%]\": \"24.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.03FA0.97\\u00a0Pb Br0.09I2.91\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.6\", \"Jsc [mA cm\\u22122]\": \"25.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1141.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\", \"PCE [%]\": \"25.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \" \", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.5\", \"Jsc [mA cm\\u22122]\": \"25.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1179.0\"}, {\"Refs.\": \"S. Tan, T. Huang, I. Yavuz, R. Wang, T. W. Yoon, M. Xu, Q. Xing, K. Park, D.-K. Lee, C.-H. Chen, R. Zheng, T. Yoon, Y. Zhao, H.-C. Wang, D. Meng, J. Xue, Y. J. Song, X. Pan, N.-G. Park, J.-W. Lee, Y. Yang, Nature 2022, 605, 268.\", \"PCE [%]\": \"24.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.95MA0.05PbBr0.15I2.85\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.3\", \"Jsc [mA cm\\u22122]\": \"25.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1158.0\"}, {\"Refs.\": \"Z. Shen, Q. Han, X. Luo, Y. Shen, T. Wang, C. Zhang, Y. Wang, H. Chen, X. Yang, Y. Zhang, L. Han, Energy Environ. Sci. 2022, 15, 1078.\", \"PCE [%]\": \"25.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.995MA0.005PbBr0.015I0.985\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.4\", \"Jsc [mA cm\\u22122]\": \"24.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1195.0\"}, {\"Refs.\": \"X. Li, W. Zhang, X. Guo, C. Lu, J. Wei, J. Fang, Science 2022, 375, 434.\", \"PCE [%]\": \"23.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.95MA0.05PbBr0.15I2.85\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.9\", \"Jsc [mA cm\\u22122]\": \"25.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1147.0\"}, {\"Refs.\": \"X. Wang, W. Sun, Y. Tu, Q. Xiong, G. Li, Z. Song, Y. Wang, Y. Du, Q. Chen, C. Deng, Z. Lan, P. Gao, J. Wu, Chem. Eng. J. 2022, 446, 137416.\", \"PCE [%]\": \"23.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.75MA0.15Rb0.05PbBr0.15I2.85\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.6\", \"Jsc [mA cm\\u22122]\": \"25.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1153.0\"}, {\"Refs.\": \"J. Peng, F. Kremer, D. Walter, Y. Wu, Y. Ji, J. Xiang, W. Liu, T. Duong, H. Shen, T. Lu, F. Brink, D. Zhong, L. Li, O. Lee Cheong Lem, Y. Liu, K. J. Weber, T. P. White, K. R. Catchpole, Nature 2022, 601, 573.\", \"PCE [%]\": \"22.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.9MA0.05PbBr0.26I2.74\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1173.0\"}, {\"Refs.\": \"Y. Zhang, N.-G. Park, ACS Energy Lett. 2022, 7, 757.\", \"PCE [%]\": \"21.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"GA(MA)5Pb5I16\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.6\", \"Jsc [mA cm\\u22122]\": \"22.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1192.0\"}, {\"Refs.\": \"S. Wang, Y. Li, J. Yang, T. Wang, B. Yang, Q. Cao, X. Pu, L. Etgar, J. Han, J. Zhao, X. Li, A. Hagfeldt, Angew. Chem., Int. Ed. 2022, 61, 202116534.\", \"PCE [%]\": \"22.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05MA0.1425FA0.8075PbBr0.45I2.55\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.8\", \"Jsc [mA cm\\u22122]\": \"23.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1130.0\"}, {\"Refs.\": \"G. Yang, Z. Ni, Z. J. Yu, B. W. Larson, Z. Yu, B. Chen, A. Alasfour, X. Xiao, J. M. Luther, Z. C. Holman, J. Huang, Nat. Photonics 2022, 16, 588.\", \"PCE [%]\": \"21.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.1FA0.2MA0.7PbBr0.45I0.2.55\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.65\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.0\", \"Jsc [mA cm\\u22122]\": \"21.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1230.0\"}, {\"Refs.\": \"S. Tan, B. Yu, Y. Cui, F. Meng, C. Huang, Y. Li, Z. Chen, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Angew. Chem., Int. Ed. 2022, 61, 202201300.\", \"PCE [%]\": \"20.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.5\", \"Jsc [mA cm\\u22122]\": \"20.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1176.0\"}, {\"Refs.\": \"S. Tan, B. Yu, Y. Cui, F. Meng, C. Huang, Y. Li, Z. Chen, H. Wu, J. Shi, Y. Luo, D. Li, Q. Meng, Angew. Chem., Int. Ed. 2022, 61, 202201300.\", \"PCE [%]\": \"20.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.7\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.8\", \"Jsc [mA cm\\u22122]\": \"20.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1177.0\"}, {\"Refs.\": \"M. A. Mahmud, J. Zheng, S. Tang, G. Wang, J. Bing, A. D. Bui, J. Qu, L. Yang, C. Liao, H. Chen, S. P. Bremner, H. T. Nguyen, J. Cairney, A. W. Y. Ho-Baillie, Adv. Energy Mater. 2022, 12, 2201672.\", \"PCE [%]\": \"20.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8PbBr0.9I2.1\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.74\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"86.5\", \"Jsc [mA cm\\u22122]\": \"19.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1210.0\"}, {\"Refs.\": \"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\", \"PCE [%]\": \"17.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.2FA0.8PbBr1.14I1.86\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.78\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.2\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1227.0\"}, {\"Refs.\": \"J. Wen, Y. Zhao, Z. Liu, H. Gao, R. Lin, S. Wan, C. Ji, K. Xiao, Y. Gao, Y. Tian, J. Xie, C. J. Brabec, H. Tan, Adv. Mater. 2022, 34, 2110356.\", \"PCE [%]\": \"17.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.4DMA0.1FA0.5PbBr0.71Cl0.15I2.14\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.1\", \"Jsc [mA cm\\u22122]\": \"17.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1255.0\"}, {\"Refs.\": \"K. Xiao, Y.-H. Lin, M. Zhang, R. D. J. Oliver, X. Wang, Z. Liu, X. Luo, J. Li, D. Lai, H. Luo, R. Lin, J. Xu, Y. Hou, H. J. Snaith, H. Tan, Science 2022, 376, 762.\", \"PCE [%]\": \"17.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.35FA0.65PbBr1.2I1.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.82\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.9\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1266.0\"}, {\"Refs.\": \"S. Qin, C. Lu, Z. Jia, Y. Wang, S. Li, W. Lai, P. Shi, R. Wang, C. Zhu, J. Du, J. Zhang, L. Meng, Y. Li, Adv. Mater. 2022, 34, 2108829.\", \"PCE [%]\": \"16.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.6MA0.4PbBr1.2I1.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.7\", \"Jsc [mA cm\\u22122]\": \"16.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1240.0\"}, {\"Refs.\": \"Z. Guo, A. K. Jena, I. Takei, M. Ikegami, A. Ishii, Y. Numata, N. Shibayama, T. Miyasaka, Adv. Funct. Mater. 2021, 31, 2103614.\", \"PCE [%]\": \"17.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBrI2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.4\", \"Jsc [mA cm\\u22122]\": \"15.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1420.0\"}, {\"Refs.\": \"W. Chen, D. Li, X. Chen, H. Chen, S. Liu, H. Yang, X. Li, Y. Shen, X. Ou, Y. Yang, L. Jiang, Y. Li, Y. Li, Adv. Funct. Mater. 2022, 32, 2109321.\", \"PCE [%]\": \"13.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbI1.8Br1.2\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.94\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.0\", \"Jsc [mA cm\\u22122]\": \"14.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1240.0\"}, {\"Refs.\": \"H. Xu, Z. Liang, J. Ye, S. Xu, Z. Wang, L. Zhu, X. Chen, Z. Xiao, X. Pan, G. Liu, Chem. Eng. J. 2022, 437, 135181.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.2\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.6\", \"Jsc [mA cm\\u22122]\": \"7.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1639.0\"}, {\"Refs.\": \"X. Li, Y. Tan, H. Lai, S. Li, Y. Chen, S. Li, P. Xu, J. Yang, ACS Appl. Mater. Interfaces 2019, 11, 29746.\", \"PCE [%]\": \"10.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.28\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"83.0\", \"Jsc [mA cm\\u22122]\": \"8.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1520.0\"}, {\"Refs.\": \"H. Zhu, L. Pan, F. T. Eickemeyer, M. A. Hope, O. Ouellette, A. Q. M. Alanazi, J. Gao, T. P. Baumeler, X. Li, S. Wang, S. M. Zakeeruddin, Y. Liu, L. Emsley, M. Gr\\u00e4tzel, ACS Energy Lett. 2022, 7, 1112.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.29\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.1\", \"Jsc [mA cm\\u22122]\": \"8.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1650.0\"}, {\"Refs.\": \"X. Yao, B. He, J. Zhu, J. Ti, L. Cui, R. Tui, M. Wei, H. Chen, J. Duan, Y. Duan, Q. Tang, Nano Energy 2022, 96, 107138.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.34\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.1\", \"Jsc [mA cm\\u22122]\": \"7.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1635.0\"}, {\"Refs.\": \"J. Zhu, Y. Liu, B. He, W. Zhang, L. Cui, S. Wang, H. Chen, Y. Duan, Q. Tang, Chem. Eng. J. 2022, 428, 131950.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPbBr3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.35\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.0\", \"Jsc [mA cm\\u22122]\": \"7.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1611.0\"}, {\"Refs.\": \"H. Yuan, Y. Zhao, J. Duan, Y. Wang, X. Yang, Q. Tang, J. Mater. Chem. A 2018, 6, 24324.\", \"PCE [%]\": \"10.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsPb0.97Tb0.03Br3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.36\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.6\", \"Jsc [mA cm\\u22122]\": \"8.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1570.0\"}, {\"Refs.\": \"B. Li, X. Wu, S. Zhang, Z. Li, D. Gao, X. Chen, S. Xiao, C.-C. Chueh, A. K. Y. Jen, Z. Zhu, Chem. Eng. J. 2022, 446, 137144.\", \"PCE [%]\": \"3.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs2AgBiBr6\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.47\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"3.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table3\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1278.0\"}, {\"Refs.\": \"W. Liu, S. Sun, S. Xu, H. Zhang, Y. Zheng, Z. Wei, X. Zhu, Adv. Mater. 2022, 34, 2200337.\", \"PCE [%]\": \"13.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTB7-Th:ATT-9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.22\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.1\", \"Jsc [mA cm\\u22122]\": \"30.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"663.0\"}, {\"Refs.\": \"Z. Liu, H.-E. Wang, Sustainable Energy Fuels 2022, 6, 744.\", \"PCE [%]\": \"13.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTR:Y6:bisPC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.32\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.1\", \"Jsc [mA cm\\u22122]\": \"20.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"916.0\"}, {\"Refs.\": \"Z. Liu, N. Wang, Sol. Energy 2021, 214, 110.\", \"PCE [%]\": \"13.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"BTR:MeIC:Y11\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"71.4\", \"Jsc [mA cm\\u22122]\": \"22.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"865.0\"}, {\"Refs.\": \"Y. Pan, X. Zheng, J. Guo, Z. Chen, S. Li, C. He, S. Ye, X. Xia, S. Wang, X. Lu, H. Zhu, J. Min, L. Zuo, M. Shi, H. Chen, Adv. Funct. Mater. 2022, 32, 2108614.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-T-3Cl:BTP-4Cl-BO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"27.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"857.0\"}, {\"Refs.\": \"L. Zhan, S. Li, Y. Li, R. Sun, J. Min, Z. Bi, W. Ma, Z. Chen, G. Zhou, H. Zhu, M. Shi, L. Zuo, H. Chen, Joule 2022, 6, 662.\", \"PCE [%]\": \"18.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:BTP-S9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"27.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"861.0\"}, {\"Refs.\": \"Y. Cai, Y. Li, R. Wang, H. Wu, Z. Chen, J. Zhang, Z. Ma, X. Hao, Y. Zhao, C. Zhang, F. Huang, Y. Sun, Adv. Mater. 2021, 33, 2101733.\", \"PCE [%]\": \"18.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:L8-BO-F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"27.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"853.0\"}, {\"Refs.\": \"Y. Cai, Y. Li, R. Wang, H. Wu, Z. Chen, J. Zhang, Z. Ma, X. Hao, Y. Zhao, C. Zhang, F. Huang, Y. Sun, Adv. Mater. 2021, 33, 2101733.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:L8-BO-F\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.8\", \"Jsc [mA cm\\u22122]\": \"27.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"847.0\"}, {\"Refs.\": \"L. Zhan, S. Li, Y. Li, R. Sun, J. Min, Z. Bi, W. Ma, Z. Chen, G. Zhou, H. Zhu, M. Shi, L. Zuo, H. Chen, Joule 2022, 6, 662.\", \"PCE [%]\": \"18.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:BTP-S9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.3\", \"Jsc [mA cm\\u22122]\": \"27.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"862.0\"}, {\"Refs.\": \"D. Wang, G. Zhou, Y. Li, K. Yan, L. Zhan, H. Zhu, X. Lu, H. Chen, C.-Z. Li, Adv. Funct. Mater. 2022, 32, 2107827.\", \"PCE [%]\": \"18.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6-1O:BO-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.5\", \"Jsc [mA cm\\u22122]\": \"27.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"848.0\"}, {\"Refs.\": \"D. Wang, G. Zhou, Y. Li, K. Yan, L. Zhan, H. Zhu, X. Lu, H. Chen, C.-Z. Li, Adv. Funct. Mater. 2022, 32, 2107827.\", \"PCE [%]\": \"18.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6-1O:BO-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"27.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"855.0\"}, {\"Refs.\": \"T. Zhang, C. An, Y. Cui, J. Zhang, P. Bi, C. Yang, S. Zhang, J. Hou, Adv. Mater. 2022, 34, 2105803.\", \"PCE [%]\": \"18.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PB2:PBDB-TF:BTP-eC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.7\", \"Jsc [mA cm\\u22122]\": \"26.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"858.0\"}, {\"Refs.\": \"L. Zuo, S. B. Jo, Y. Li, Y. Meng, R. J. Stoddard, Y. Liu, F. Lin, X. Shi, F. Liu, H. W. Hillhouse, D. S. Ginger, H. Chen, A. K. Y. Jen, Nat. Nanotechnol. 2022, 17, 53.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC11:BTP-S2\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"26.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"872.0\"}, {\"Refs.\": \"X. Duan, W. Song, J. Qiao, X. Li, Y. Cai, H. Wu, J. Zhang, X. Hao, Z. Tang, Z. Ge, F. Huang, Y. Sun, Energy Environ. Sci. 2022, 15, 1563.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:ZY-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.9\", \"Jsc [mA cm\\u22122]\": \"27.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"863.0\"}, {\"Refs.\": \"X. Duan, W. Song, J. Qiao, X. Li, Y. Cai, H. Wu, J. Zhang, X. Hao, Z. Tang, Z. Ge, F. Huang, Y. Sun, Energy Environ. Sci. 2022, 15, 1563.\", \"PCE [%]\": \"18.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:ZY-4Cl\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"27.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"863.0\"}, {\"Refs.\": \"S. Guan, Y. Li, K. Yan, W. Fu, L. Zuo, H. Chen, Adv. Mater. 2022, 34, 2205844.\", \"PCE [%]\": \"19.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:L8-BO:BTP-eC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.9\", \"Jsc [mA cm\\u22122]\": \"27.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"869.0\"}, {\"Refs.\": \"S. Guan, Y. Li, K. Yan, W. Fu, L. Zuo, H. Chen, Adv. Mater. 2022, 34, 2205844.\", \"PCE [%]\": \"19.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-TF:L8-BO:BTP-eC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.2\", \"Jsc [mA cm\\u22122]\": \"27.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"863.0\"}, {\"Refs.\": \"C. He, Z. Bi, Z. Chen, J. Guo, X. Xia, X. Lu, J. Min, H. Zhu, W. Ma, L. Zuo, H. Chen, Adv. Funct. Mater. 2022, 32, 2112511.\", \"PCE [%]\": \"18.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:AC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"867.0\"}, {\"Refs.\": \"W. Feng, S. Wu, H. Chen, L. Meng, F. Huang, H. Liang, J. Zhang, Z. Wei, X. Wan, C. Li, Z. Yao, Y. Chen, Adv. Energy Mater. 2022, 12, 2104060.\", \"PCE [%]\": \"18.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:CNS-6-8:Y6:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.8\", \"Jsc [mA cm\\u22122]\": \"26.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"868.0\"}, {\"Refs.\": \"C. He, Z. Bi, Z. Chen, J. Guo, X. Xia, X. Lu, J. Min, H. Zhu, W. Ma, L. Zuo, H. Chen, Adv. Funct. Mater. 2022, 32, 2112511.\", \"PCE [%]\": \"18.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:AC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.1\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"871.0\"}, {\"Refs.\": \"B. Fan, W. Gao, X. Wu, X. Xia, Y. Wu, F. R. Lin, Q. Fan, X. Lu, W. J. Li, W. Ma, A. K. Y. Jen, Nat. Commun. 2022, 13, 5946.\", \"PCE [%]\": \"18.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PTzBI-dF:BTP-TBr\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.8\", \"Jsc [mA cm\\u22122]\": \"27.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"845.0\"}, {\"Refs.\": \"R. Yu, X. Wei, G. Wu, T. Zhang, Y. Gong, B. Zhao, J. Hou, C. Yang, Z. Tan, Energy Environ. Sci. 2022, 15, 822.\", \"PCE [%]\": \"18.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:PB2F:BTP-eC9\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"26.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"Y. Cui, Y. Xu, H. Yao, P. Bi, L. Hong, J. Zhang, Y. Zu, T. Zhang, J. Qin, J. Ren, Z. Chen, C. He, X. Hao, Z. Wei, J. Hou, Adv. Mater. 2021, 33, 2102420.\", \"PCE [%]\": \"19.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBQx-TF:eC9-2Cl:F-BTA3\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.0\", \"Jsc [mA cm\\u22122]\": \"26.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"879.0\"}, {\"Refs.\": \"Y. Cui, Y. Xu, H. Yao, P. Bi, L. Hong, J. Zhang, Y. Zu, T. Zhang, J. Qin, J. Ren, Z. Chen, C. He, X. Hao, Z. Wei, J. Hou, Adv. Mater. 2021, 33, 2102420.\", \"PCE [%]\": \"18.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBQx-TF:eC9-2Cl:F-BTA3\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"878.0\"}, {\"Refs.\": \"J. Zhang, F. Bai, I. Angunawela, X. Xu, S. Luo, C. Li, G. Chai, H. Yu, Y. Chen, H. Hu, Z. Ma, H. Ade, H. Yan, Adv. Energy Mater. 2021, 11, 2102596.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:BTP-4F-P2EH\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.1\", \"Jsc [mA cm\\u22122]\": \"25.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"880.0\"}, {\"Refs.\": \"J. Song, L. Zhu, C. Li, J. Xu, H. Wu, X. Zhang, Y. Zhang, Z. Tang, F. Liu, Y. Sun, Matter 2021, 4, 2542.\", \"PCE [%]\": \"18.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:L8-BO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.0\", \"Jsc [mA cm\\u22122]\": \"26.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"893.0\"}, {\"Refs.\": \"J. Song, L. Zhu, C. Li, J. Xu, H. Wu, X. Zhang, Y. Zhang, Z. Tang, F. Liu, Y. Sun, Matter 2021, 4, 2542.\", \"PCE [%]\": \"18.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:L8-BO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"26.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"883.0\"}, {\"Refs.\": \"L. Zhu, M. Zhang, J. Xu, C. Li, J. Yan, G. Zhou, W. Zhong, T. Hao, J. Song, X. Xue, Z. Zhou, R. Zeng, H. Zhu, C.-C. Chen, R. C. I. MacKenzie, Y. Zou, J. Nelson, Y. Zhang, Y. Sun, F. Liu, Nat. Mater. 2022, 21, 656.\", \"PCE [%]\": \"19.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:D18:L8-BO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.9\", \"Jsc [mA cm\\u22122]\": \"26.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"896.0\"}, {\"Refs.\": \"Y. Wei, Z. Chen, G. Lu, N. Yu, C. Li, J. Gao, X. Gu, X. Hao, G. Lu, Z. Tang, J. Zhang, Z. Wei, X. Zhang, H. Huang, Adv. Mater. 2022, 34, 2204718.\", \"PCE [%]\": \"19.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"D18:L8-BO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"26.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"918.0\"}, {\"Refs.\": \"L. Zhu, M. Zhang, J. Xu, C. Li, J. Yan, G. Zhou, W. Zhong, T. Hao, J. Song, X. Xue, Z. Zhou, R. Zeng, H. Zhu, C.-C. Chen, R. C. I. MacKenzie, Y. Zou, J. Nelson, Y. Zhang, Y. Sun, F. Liu, Nat. Mater. 2022, 21, 656.\", \"PCE [%]\": \"19.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:D18:L8-BO\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.7\", \"Jsc [mA cm\\u22122]\": \"26.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"891.0\"}, {\"Refs.\": \"Y. Li, J. Song, Y. Dong, H. Jin, J. Xin, S. Wang, Y. Cai, L. Jiang, W. Ma, Z. Tang, Y. Sun, Adv. Mater. 2022, 34, 2110155.\", \"PCE [%]\": \"16.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:PY-DT\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.4\", \"Jsc [mA cm\\u22122]\": \"23.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table4\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"949.0\"}, {\"Refs.\": \"S. Mathew, A. Yella, P. Gao, R. Humphry-Baker, B. F. E. Curchod, N. Ashari-Astani, I. Tavernelli, U. Rothlisberger, M. K. Nazeeruddin, M. Gr\\u00e4tzel, Nat. Chem. 2014, 6, 242.\", \"PCE [%]\": \"13.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.66\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.0\", \"Jsc [mA cm\\u22122]\": \"18.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SM315\", \"Table\": \"ver3_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"910.0\"}, {\"Refs.\": \"S. Mathew, A. Yella, P. Gao, R. Humphry-Baker, B. F. E. Curchod, N. Ashari-Astani, I. Tavernelli, U. Rothlisberger, M. K. Nazeeruddin, M. Gr\\u00e4tzel, Nat. Chem. 2014, 6, 242.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.76\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.0\", \"Jsc [mA cm\\u22122]\": \"15.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SM371\", \"Table\": \"ver3_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"960.0\"}, {\"Refs.\": \"P.-H. Chang, M. C. Sil, K. S. K. Reddy, C.-H. Lin, C.-M. Chen, ACS Appl. Mater. Interfaces 2022, 14, 25466.\", \"PCE [%]\": \"9.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.79\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.5\", \"Jsc [mA cm\\u22122]\": \"19.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"PI-COF:N719\", \"Table\": \"ver3_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"740.0\"}, {\"Refs.\": \"A. K. Bharwal, L. Manceriu, C. Olivier, A. Mahmoud, C. Iojoiu, T. Toupance, C. M. Ruiz, M. Pasquinelli, D. Duch\\u00e9, J.-J. Simon, C. Henrist, F. Alloin, Chem. Eng. J. 2022, 446, 136777.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.6\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver3_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"700.0\"}, {\"Refs.\": \"Y. Ren, D. Zhang, J. Suo, Y. Cao, F. T. Eickemeyer, N. Vlachopoulos, S. M. Zakeeruddin, A. Hagfeldt, M. Gr\\u00e4tzel, Nature 2022, https://doi.org/10.1038/s41586-022-05460-z.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.83\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"18.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"SL9 + SL10/BPHA\", \"Table\": \"ver3_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1063.0\"}, {\"Refs.\": \"C. Liao, H. Wu, H. Tang, L. Wang, D. Cao, Sol. Energy 2022, 240, 399.\", \"PCE [%]\": \"4.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.15\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.6\", \"Jsc [mA cm\\u22122]\": \"8.76\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"PS1\", \"Table\": \"ver3_table5\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"640.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.1\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.9\", \"Jsc [mA cm\\u22122]\": \"36.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"538.0\"}, {\"Refs.\": \"J. Wang, J. Zhou, X. Xu, F. Meng, C. Xiang, L. Lou, K. Yin, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, H. Xin, Q. Meng, Adv. Mater. 2022, 34, 2202858.\", \"PCE [%]\": \"13.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.0\", \"Jsc [mA cm\\u22122]\": \"34.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"547.0\"}, {\"Refs.\": \"J. Wang, J. Zhou, X. Xu, F. Meng, C. Xiang, L. Lou, K. Yin, B. Duan, H. Wu, J. Shi, Y. Luo, D. Li, H. Xin, Q. Meng, Adv. Mater. 2022, 34, 2202858.\", \"PCE [%]\": \"12.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Cu2ZnSn(S,Se)4\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.9\", \"Jsc [mA cm\\u22122]\": \"35.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"526.0\"}, {\"Refs.\": \"R. Tang, S. Chen, Z.-H. Zheng, Z.-H. Su, J.-T. Luo, P. Fan, X.-H. Zhang, J. Tang, G.-X. Liang, Adv. Mater. 2022, 34, 2109078.\", \"PCE [%]\": \"8.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2Se3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.33\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"59.8\", \"Jsc [mA cm\\u22122]\": \"27.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"520.0\"}, {\"Refs.\": \"Y. Wang, L. Peng, Z. Wang, G. Konstantatos, Adv. Energy Mater. 2022, 12, 2200700.\", \"PCE [%]\": \"7.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"AgBiS2\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.0\", \"Jsc [mA cm\\u22122]\": \"24.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"480.0\"}, {\"Refs.\": \"Y. Wang, S. R. Kavanagh, I. Burgu\\u00e9s-Ceballos, A. Walsh, D. O. Scanlon, G. Konstantatos, Nat. Photonics 2022, 16, 235.\", \"PCE [%]\": \"8.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"AgBiS2\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.5\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"482.0\"}, {\"Refs.\": \"Y. Wang, S. R. Kavanagh, I. Burgu\\u00e9s-Ceballos, A. Walsh, D. O. Scanlon, G. Konstantatos, Nat. Photonics 2022, 16, 235.\", \"PCE [%]\": \"9.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"AgBiS2\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.4\", \"Jsc [mA cm\\u22122]\": \"27.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"495.0\"}, {\"Refs.\": \"R. Tang, X. Wang, W. Lian, J. Huang, Q. Wei, M. Huang, Y. Yin, C. Jiang, S. Yang, G. Xing, S. Chen, C. Zhu, X. Hao, M. A. Green, T. Chen, Nat. Energy 2020, 5, 587.\", \"PCE [%]\": \"10.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2(S,Se)3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.3\", \"Jsc [mA cm\\u22122]\": \"24.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"655.0\"}, {\"Refs.\": \"Y. Zhao, S. Wang, C. Jiang, C. Li, P. Xiao, R. Tang, J. Gong, G. Chen, T. Chen, J. Li, X. Xiao, Adv. Energy Mater. 2022, 12, 2103015.\", \"PCE [%]\": \"10.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2(S,Se)3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.8\", \"Jsc [mA cm\\u22122]\": \"23.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"673.0\"}, {\"Refs.\": \"C. Jiang, J. Zhou, R. Tang, W. Lian, X. Wang, X. Lei, H. Zeng, C. Zhu, W. Tang, T. Chen, Energy Environ. Sci. 2021, 14, 359.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2(S,Se)3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.5\", \"Jsc [mA cm\\u22122]\": \"23.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"638.0\"}, {\"Refs.\": \"X. Wang, R. Tang, C. Jiang, W. Lian, H. Ju, G. Jiang, Z. Li, C. Zhu, T. Chen, Adv. Energy Mater. 2020, 10, 2002341.\", \"PCE [%]\": \"10.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2(S,Se)3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.55\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.3\", \"Jsc [mA cm\\u22122]\": \"23.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"664.0\"}, {\"Refs.\": \"S. Wang, Y. Zhao, B. Che, C. Li, X. Chen, R. Tang, J. Gong, X. Wang, G. Chen, T. Chen, J. Li, X. Xiao, Adv. Mater. 2022, 34, 2206242.\", \"PCE [%]\": \"8.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Sb2S3\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.73\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"17.4\", \"Jsc [mA cm\\u22122]\": \"60.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table6\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"757.0\"}, {\"Refs.\": \"Z. Sun, M. Liu, Y. Zhou, Q. Wang, Y. Yang, Y. Zhou, F. Liu, Sol. Energy Mater. Sol. Cells 2022, 235, 111453.\", \"PCE [%]\": \"20.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"Si\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.18\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.7\", \"Jsc [mA cm\\u22122]\": \"40.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table7\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"706.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\", \"PCE [%]\": \"29.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"1.69\", \"FF [%]\": \"79.8\", \"Jsc [mA cm\\u22122]\": \"19.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \" \", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1190.0\"}, {\"Refs.\": \"L. Mao, T. Yang, H. Zhang, J. Shi, Y. Hu, P. Zeng, F. Li, J. Gong, X. Fang, Y. Sun, X. Liu, J. Du, A. Han, L. Zhang, W. Liu, F. Meng, X. Cui, Z. Liu, M. Liu, Adv. Mater. 2022, 34, 2206193.\", \"PCE [%]\": \"28.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.13\", \"Eg,middle, Eg,top [eV]\": \"1.67\", \"FF [%]\": \"79.6\", \"Jsc [mA cm\\u22122]\": \"20.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"FAMAPb(BrClI)3\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1776.0\"}, {\"Refs.\": \"Y. Wu, P. Zheng, J. Peng, M. Xu, Y. Chen, S. Surve, T. Lu, A. D. Bui, N. Li, W. Liang, L. Duan, B. Li, H. Shen, T. Duong, J. Yang, X. Zhang, Y. Liu, H. Jin, Q. Chen, T. White, K. Catchpole, H. Zhou, K. Weber, Adv. Energy Mater. 2022, 12, 2200821.\", \"PCE [%]\": \"27.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.14\", \"Eg,middle, Eg,top [eV]\": \"1.68\", \"FF [%]\": \"78.9\", \"Jsc [mA cm\\u22122]\": \"19.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.22FA0.78PbBr0.45Cl0.09I2.55\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1779.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\", \"PCE [%]\": \"26.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.14\", \"Eg,middle, Eg,top [eV]\": \"1.69\", \"FF [%]\": \"79.4\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \" \", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1891.0\"}, {\"Refs.\": \"K. Liu, B. Chen, Z. J. Yu, Y. Wu, Z. Huang, X. Jia, C. Li, D. Spronk, Z. Wang, Z. Wang, S. Qu, Z. C. Holman, J. Huang, J. Mater. Chem. A 2022, 10, 1343.\", \"PCE [%]\": \"26.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.14\", \"Eg,middle, Eg,top [eV]\": \"1.69\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"18.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.15FA0.7055MA0.1445PbBr0.6I2.4\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1780.0\"}, {\"Refs.\": \"M. A. Ruiz-Preciado, F. Gota, P. Fassl, I. M. Hossain, R. Singh, F. Laufer, F. Schackmar, T. Feeney, A. Farag, I. Allegro, H. Hu, S. Gharibzadeh, B. A. Nejand, V. S. Gevaerts, M. Simor, P. J. Bolt, U. W. Paetzold, ACS Energy Lett. 2022, 7, 2273.\", \"PCE [%]\": \"24.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CuInSe2\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.01\", \"Eg,middle, Eg,top [eV]\": \"1.61\", \"FF [%]\": \"73.6\", \"Jsc [mA cm\\u22122]\": \"21.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.05FA0.85MA0.1PbI2.7Br0.3\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1570.0\"}, {\"Refs.\": \"M. A. Ruiz-Preciado, F. Gota, P. Fassl, I. M. Hossain, R. Singh, F. Laufer, F. Schackmar, T. Feeney, A. Farag, I. Allegro, H. Hu, S. Gharibzadeh, B. A. Nejand, V. S. Gevaerts, M. Simor, P. J. Bolt, U. W. Paetzold, ACS Energy Lett. 2022, 7, 2273.\", \"PCE [%]\": \"23.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CuInSe2\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.01\", \"Eg,middle, Eg,top [eV]\": \"1.61\", \"FF [%]\": \"75.5\", \"Jsc [mA cm\\u22122]\": \"19.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.05FA0.85MA0.1PbI2.7Br0.3\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1590.0\"}, {\"Refs.\": \"M. Jo\\u0161t, E. K\\u00f6hnen, A. Al-Ashouri, T. Bertram, \\u0160. Tom\\u0161i\\u010d, A. Magomedov, E. Kasparavicius, T. Kodalle, B. Lipov\\u0161ek, V. Getautis, R. Schlatmann, C. A. Kaufmann, S. Albrecht, M. Topi\\u010d, ACS Energy Lett. 2022, 7, 1298.\", \"PCE [%]\": \"24.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"CIGS\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.11\", \"Eg,middle, Eg,top [eV]\": \"1.68\", \"FF [%]\": \"71.2\", \"Jsc [mA cm\\u22122]\": \"18.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.05FA0.7315MA0.2185PbBr0.69I2.31\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1770.0\"}, {\"Refs.\": \"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\", \"PCE [%]\": \"26.3 (26.4) \", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Cs0.2FA0.8\\u00a0Pb Br1.14I1.86\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.25\", \"Eg,middle, Eg,top [eV]\": \"1.80\", \"FF [%]\": \"78.1\", \"Jsc [mA cm\\u22122]\": \"16.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2044.0\"}, {\"Refs.\": \"K. Datta, J. Wang, D. Zhang, V. Zardetto, W. H. M. Remmerswaal, C. H. L. Weijtens, M. M. Wienk, R. A. J. Janssen, Adv. Mater. 2022, 34, 2110053.\", \"PCE [%]\": \"23.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.66MA0.34Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"1.79\", \"FF [%]\": \"75.0\", \"Jsc [mA cm\\u22122]\": \"15.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.05(FAMA0.95)K0.05Pb(BrI)3\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1950.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\", \"PCE [%]\": \"28.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \" \", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"1.80\", \"FF [%]\": \"80.2\", \"Jsc [mA cm\\u22122]\": \"16.42\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \" \", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2125.0\"}, {\"Refs.\": \"J. Wen, Y. Zhao, Z. Liu, H. Gao, R. Lin, S. Wan, C. Ji, K. Xiao, Y. Gao, Y. Tian, J. Xie, C. J. Brabec, H. Tan, Adv. Mater. 2022, 34, 2110356.\", \"PCE [%]\": \"26.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"1.80\", \"FF [%]\": \"80.1\", \"Jsc [mA cm\\u22122]\": \"16.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.4DMA0.1FA0.5PbBr0.71Cl0.15I2.14\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2040.0\"}, {\"Refs.\": \"H. Gao, Q. Lu, K. Xiao, Q. Han, R. Lin, Z. Liu, H. Li, L. Li, X. Luo, Y. Gao, Y. Wang, J. Wen, Z. Zou, Y. Zhou, H. Tan, Sol. RRL 2021, 5, 2100814.\", \"PCE [%]\": \"23.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Cs0.2FA0.8Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.27\", \"Eg,middle, Eg,top [eV]\": \"1.82\", \"FF [%]\": \"79.8\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.2FA0.8PbBr1.2I1.8\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1890.0\"}, {\"Refs.\": \"S. Qin, C. Lu, Z. Jia, Y. Wang, S. Li, W. Lai, P. Shi, R. Wang, C. Zhu, J. Du, J. Zhang, L. Meng, Y. Li, Adv. Mater. 2022, 34, 2108829.\", \"PCE [%]\": \"21.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"PTB7-Th:BTPV-4Cl-eC9\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.21\", \"Eg,middle, Eg,top [eV]\": \"1.83\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"15.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"FA0.6MA0.4PbBr1.2I1.8\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1880.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, K. Bothe, D. Hinken, M. Rauer, X. Hao, Prog. Photovoltaics 2022, 30, 687.\", \"PCE [%]\": \"23.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \" \", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.38\", \"Eg,middle, Eg,top [eV]\": \"1.88\", \"FF [%]\": \"75.2\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \" \", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2136.0\"}, {\"Refs.\": \"J. Zheng, G. Wang, W. Duan, M. A. Mahmud, H. Yi, C. Xu, A. Lambertz, S. Bremner, K. Ding, S. Huang, A. W. Y. Ho-Baillie, ACS Energy Lett. 2022, 7, 3003.\", \"PCE [%]\": \"20.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Si\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.13\", \"Eg,middle, Eg,top [eV]\": \"1.54, 1.91\", \"FF [%]\": \"86.0\", \"Jsc [mA cm\\u22122]\": \"8.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.1FA0.9PbI3, Cs0.2FA0.8PbBr1.65I1.35\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2740.0\"}, {\"Refs.\": \"J. Wang, V. Zardetto, K. Datta, D. Zhang, M. M. Wienk, R. A. J. Janssen, Nat. Commun. 2020, 11, 5254.\", \"PCE [%]\": \"16.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.66MA0.34Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.23\", \"Eg,middle, Eg,top [eV]\": \"1.57, 1.78\", \"FF [%]\": \"81.0\", \"Jsc [mA cm\\u22122]\": \"7.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"FA0.66MA0.34\\u00a0Pb Br0.15I2.85, Cs0.1FA0.594MA0.306PbBrI2\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2780.0\"}, {\"Refs.\": \"K. Xiao, J. Wen, Q. Han, R. Lin, Y. Gao, S. Gu, Y. Zang, Y. Nie, J. Zhu, J. Xu, H. Tan, ACS Energy Lett. 2020, 5, 2819.\", \"PCE [%]\": \"19.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"1.65, 2.06\", \"FF [%]\": \"80.7\", \"Jsc [mA cm\\u22122]\": \"8.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"Cs0.05FA0.95PbBr0.45 I2.55, Cs0.2FA0.8PbBr2.1I0.9\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table8\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2793.0\"}, {\"Refs.\": \"Y. Huang, L. Meng, H. Liang, M. Li, H. Chen, C. Jiang, K. Zhang, F. Huang, Z. Yao, C. Li, X. Wan, Y. Chen, J. Mater. Chem. A 2022, 10, 11238.\", \"PCE [%]\": \"18.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PM6:CH1007:PC71BM\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.73\", \"Eg,bottom [eV]\": \"1.36\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.9\", \"Jsc [mA cm\\u22122]\": \"14.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table9\", \"Top absorber\": \"D18:F-ThBr\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1883.0\"}, {\"Refs.\": \"Z. Zheng, J. Wang, P. Bi, J. Ren, Y. Wang, Y. Yang, X. Liu, S. Zhang, J. Hou, Joule 2022, 6, 171.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PBDB-TF:GS-ISO\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.8\", \"Eg,bottom [eV]\": \"1.38\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.8\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table9\", \"Top absorber\": \"PBDM-TF:BTp-eC9\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2010.0\"}, {\"Refs.\": \"Z. Zheng, J. Wang, P. Bi, J. Ren, Y. Wang, Y. Yang, X. Liu, S. Zhang, J. Hou, Joule 2022, 6, 171.\", \"PCE [%]\": \"20.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"PBDB-TF:GS-ISO\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.8\", \"Eg,bottom [eV]\": \"1.38\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.8\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table9\", \"Top absorber\": \"PBDM-TF:BTp-eC9\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2010.0\"}, {\"Refs.\": \"S. H. Kang, M. J. Jeong, Y. K. Eom, I. T. Choi, S. M. Kwon, Y. Yoo, J. Kim, J. Kwon, J. H. Park, H. K. Kim, Adv. Energy Mater. 2017, 7, 1602117.\", \"PCE [%]\": \"12.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"SGT-121/HC-A1\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.98\", \"Eg,bottom [eV]\": \"1.67\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.0\", \"Jsc [mA cm\\u22122]\": \"10.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table9\", \"Top absorber\": \"SGT-021/HC-A4\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1825.0\"}, {\"Refs.\": \"R. M. France, J. F. Geisz, T. Song, W. Olavarria, M. Young, A. Kibbler, M. A. Steiner, Joule 2022, 6, 1121.\", \"PCE [%]\": \"39.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"InGaAs\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"0.92\", \"Eg,middle, Eg,top [eV]\": \"1.33, 1.88\", \"FF [%]\": \"85.3\", \"Jsc [mA cm\\u22122]\": \"15.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"GaAs, InGaP\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"3000.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, Prog. Photovoltaics 2013, 21, 1.\", \"PCE [%]\": \"37.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"InGaAs\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"0.98\", \"Eg,middle, Eg,top [eV]\": \"1.41, 1.89\", \"FF [%]\": \"86.0\", \"Jsc [mA cm\\u22122]\": \"14.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"GaAs, InGaP\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"3014.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 657.\", \"PCE [%]\": \"35.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"Si\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.13\", \"Eg,middle, Eg,top [eV]\": \"1.48, 1.93\", \"FF [%]\": \"84.3\", \"Jsc [mA cm\\u22122]\": \"13.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"GaInAsP, InGaP\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"3248.0\"}, {\"Refs.\": \"M. A. Green, E. D. Dunlop, J. Hohl-Ebinger, M. Yoshita, N. Kopidakis, X. Hao, Prog. Photovoltaics 2021, 29, 657.\", \"PCE [%]\": \"28.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"CIGS\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.01\", \"Eg,middle, Eg,top [eV]\": \"1.50, 1.92\", \"FF [%]\": \"81.1\", \"Jsc [mA cm\\u22122]\": \"11.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"AlGaAs/GaInP\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"2952.0\"}, {\"Refs.\": \"M. A. Green, K. Emery, Y. Hishikawa, W. Warta, E. D. Dunlop, D. H. Levi, A. W. Y. Ho-Baillie, Prog. Photovoltaics 2017, 25, 3.\", \"PCE [%]\": \"14.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"nc-Si\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"1.3\", \"Eg,middle, Eg,top [eV]\": \"1.27, 2.03\", \"FF [%]\": \"73.4\", \"Jsc [mA cm\\u22122]\": \"9.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"nc-Si, a-Si\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table10\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1922.0\"}, {\"Refs.\": \"Y. Wang, T. Li, X. Chen, L. Zhang, Mater. Lett. 2022, 321, 132460.\", \"PCE [%]\": \"5.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FA0.8MA0.2SnBr0.2I2.8\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.7\", \"Jsc [mA cm\\u22122]\": \"17.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"462.0\"}, {\"Refs.\": \"M. Chen, Q. Dong, C. Xiao, X. Zheng, Z. Dai, Y. Shi, J. M. Luther, N. P. Padture, ACS Energy Lett. 2022, 7, 2256.\", \"PCE [%]\": \"8.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAGe0.1Sn0.9I3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.44\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.9\", \"Jsc [mA cm\\u22122]\": \"20.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"650.0\"}, {\"Refs.\": \"M. Chen, Q. Dong, C. Xiao, X. Zheng, Z. Dai, Y. Shi, J. M. Luther, N. P. Padture, ACS Energy Lett. 2022, 7, 2256.\", \"PCE [%]\": \"20.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAMAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.2\", \"Jsc [mA cm\\u22122]\": \"23.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1070.0\"}, {\"Refs.\": \"Z. Zheng, F. Li, J. Gong, Y. Ma, J. Gu, X. Liu, S. Chen, M. Liu, Adv. Mater. 2022, 34, 2109879.\", \"PCE [%]\": \"22.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAMAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.9\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1151.0\"}, {\"Refs.\": \"L. Yang, J. Feng, Z. Liu, Y. Duan, S. Zhan, S. Yang, K. He, Y. Li, Y. Zhou, N. Yuan, J. Ding, S. Liu, Adv. Mater. 2022, 34, 2201681.\", \"PCE [%]\": \"22.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.1FA0.9PbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.54\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.8\", \"Jsc [mA cm\\u22122]\": \"24.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1170.0\"}, {\"Refs.\": \"S. Wu, Z. Li, J. Zhang, X. Wu, X. Deng, Y. Liu, J. Zhou, C. Zhi, X. Yu, W. C. H. Choy, Z. Zhu, A. K. Y. Jen, Adv. Mater. 2021, 33, 2105539.\", \"PCE [%]\": \"21.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.05FA0.931MA0.019PbBr0.06I2.94/PM6:CH1007:PCBM\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.56\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.7\", \"Jsc [mA cm\\u22122]\": \"24.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1127.0\"}, {\"Refs.\": \"X. Meng, X. Hu, Y. Zhang, Z. Huang, Z. Xing, C. Gong, L. Rao, H. Wang, F. Wang, T. Hu, L. Tan, Y. Song, Y. Chen, Adv. Funct. Mater. 2021, 31, 2106460.\", \"PCE [%]\": \"20.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"FAMAPbBrI\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.1\", \"Jsc [mA cm\\u22122]\": \"22.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"B. Fan, J. Xiong, Y. Zhang, C. Gong, F. Li, X. Meng, X. Hu, Z. Yuan, F. Wang, Y. Chen, Adv. Mater. 2022, 34, 2201840.\", \"PCE [%]\": \"20.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsFAMAPbBrI\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.7\", \"Jsc [mA cm\\u22122]\": \"23.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1110.0\"}, {\"Refs.\": \"Q. Dong, M. Chen, Y. Liu, F. T. Eickemeyer, W. Zhao, Z. Dai, Y. Yin, C. Jiang, J. Feng, S. Jin, S. Liu, S. M. Zakeeruddin, M. Gr\\u00e4tzel, N. P. Padture, Y. Shi, Joule 2021, 5, 1587.\", \"PCE [%]\": \"20.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"Cs0.04FA0.86MA0.1PbBr0.29I2.71\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.5\", \"Jsc [mA cm\\u22122]\": \"23.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1140.0\"}, {\"Refs.\": \"B. Fan, J. Xiong, Y. Zhang, C. Gong, F. Li, X. Meng, X. Hu, Z. Yuan, F. Wang, Y. Chen, Adv. Mater. 2022, 34, 2201840.\", \"PCE [%]\": \"17.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"CsFAMAPbBrI\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"21.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1060.0\"}, {\"Refs.\": \"P. Sun, G. Qu, Q. Hu, Y. Ma, H. Liu, Z.-X. Xu, Z. Huang, ACS Appl. Energy Mater. 2022, 5, 3568.\", \"PCE [%]\": \"14.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"MAPbI3\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.3\", \"Jsc [mA cm\\u22122]\": \"21.5\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table11\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1030.0\"}, {\"Refs.\": \"Y. Han, Z. Hu, W. Zha, X. Chen, L. Yin, J. Guo, Z. Li, Q. Luo, W. Su, C.-Q. Ma, Adv. Mater. 2022, 34, 2110276.\", \"PCE [%]\": \"16.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-4Cl-12\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.36\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.4\", \"Jsc [mA cm\\u22122]\": \"26.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"821.0\"}, {\"Refs.\": \"Y. Han, Z. Hu, W. Zha, X. Chen, L. Yin, J. Guo, Z. Li, Q. Luo, W. Su, C.-Q. Ma, Adv. Mater. 2022, 34, 2110276.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-4Cl-12\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"67.4\", \"Jsc [mA cm\\u22122]\": \"21.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"827.0\"}, {\"Refs.\": \"G. Zeng, W. Chen, X. Chen, Y. Hu, Y. Chen, B. Zhang, H. Chen, W. Sun, Y. Shen, Y. Li, F. Yan, Y. Li, J. Am. Chem. Soc. 2022, 144, 8658.\", \"PCE [%]\": \"17.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:BTP-eC9:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.38\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.7\", \"Jsc [mA cm\\u22122]\": \"27.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"835.0\"}, {\"Refs.\": \"Z. Chen, W. Song, K. Yu, J. Ge, J. Zhang, L. Xie, R. Peng, Z. Ge, Joule 2021, 5, 2395.\", \"PCE [%]\": \"15.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"D-18-Cl:G19:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.5\", \"Jsc [mA cm\\u22122]\": \"25.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"864.0\"}, {\"Refs.\": \"Y. Chen, J. Wan, G. Xu, X. Wu, X. Li, Y. Shen, F. Yang, X. Ou, Y. Li, Y. Li, Sci China Chem 2022, 65, 1164.\", \"PCE [%]\": \"17.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PBDB-T-2F:BTP-eC9:PC71BM\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.9\", \"Jsc [mA cm\\u22122]\": \"27.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"N. Cui, Y. Song, C.-H. Tan, K. Zhang, X. Yang, S. Dong, B. Xie, F. Huang, npj Flexible Electron. 2021, 5, 31.\", \"PCE [%]\": \"15.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"PM6:Y6\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.3\", \"Jsc [mA cm\\u22122]\": \"25.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table12\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"B. Murali, K. Gireesh Baiju, R. Krishna Prasad, K. Jayanarayanan, D. Kumaresan, Sustainable Energy Fuels 2022, 6, 2503.\", \"PCE [%]\": \"3.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"2.02\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"45.2\", \"Jsc [mA cm\\u22122]\": \"11.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver3_table13\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"720.0\"}, {\"Refs.\": \"J. Sch\\u00f6n, G. M. M. W. Bissels, P. Mulder, R. H. van Leest, N. Gruginskie, E. Vlieg, D. Chojniak, D. Lackner, Prog. Photovoltaics 2022, 30, 1003.\", \"PCE [%]\": \"30.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"Ga0.73In0.27As\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.41, 1.91 \", \"Eg,bottom [eV]\": \"1.0\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"84.5\", \"Jsc [mA cm\\u22122]\": \"16.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"GaAs, Ga0.51In0.49P \", \"Voc [mV]\": \"3043.0\"}, {\"Refs.\": \"L. Li, Y. Wang, X. Wang, R. Lin, X. Luo, Z. Liu, K. Zhou, S. Xiong, Q. Bao, G. Chen, Y. Tian, Y. Deng, K. Xiao, J. Wu, M. I. Saidaminov, H. Lin, C.-Q. Ma, Z. Zhao, Y. Wu, L. Zhang, H. Tan, Nat. Energy 2022, 7, 708.\", \"PCE [%]\": \"24.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.78\", \"Eg,bottom [eV]\": \"1.25\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.3\", \"Jsc [mA cm\\u22122]\": \"15.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8Cs0.2PbI1.95Br1.05\", \"Voc [mV]\": \"2000.0\"}, {\"Refs.\": \"L. Li, Y. Wang, X. Wang, R. Lin, X. Luo, Z. Liu, K. Zhou, S. Xiong, Q. Bao, G. Chen, Y. Tian, Y. Deng, K. Xiao, J. Wu, M. I. Saidaminov, H. Lin, C.-Q. Ma, Z. Zhao, Y. Wu, L. Zhang, H. Tan, Nat. Energy 2022, 7, 708.\", \"PCE [%]\": \"24.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.78\", \"Eg,bottom [eV]\": \"1.25\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.3\", \"Jsc [mA cm\\u22122]\": \"15.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.8Cs0.2PbI1.95Br1.05\", \"Voc [mV]\": \"2016.0\"}, {\"Refs.\": \"H. Lai, J. Luo, Y. Zwirner, S. Olthof, A. Wieczorek, F. Ye, Q. Jeangros, X. Yin, F. Akhundova, T. Ma, R. He, R. K. Kothandaraman, X. Chin, E. Gilshtein, A. M\\u00fcller, C. Wang, J. Thiesbrummel, S. Siol, J. M. Prieto, T. Unold, M. Stolterfoht, C. Chen, A. N. Tiwari, D. Zhao, F. Fu, Adv. Energy Mater. 2022, 12, 2202438.\", \"PCE [%]\": \"23.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.6MA0.4Pb0.4Sn0.6I3\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.79\", \"Eg,bottom [eV]\": \"1.26\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.1\", \"Jsc [mA cm\\u22122]\": \"15.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table14\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"Cs0.12FA0.8MA0.08PbI1.8Br1.2\", \"Voc [mV]\": \"2.1\"}, {\"Refs.\": \"L. Sun, W. Wang, L. Hao, Z. Jia, Y. Zhao, G. Zhi, H. Yao, Mater. Sci. Semicond. Process. 2022, 138, 106301.\", \"PCE [%]\": \"4.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"Cu2CdxZn1 xSn(S,Se)4\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.04\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"46.4\", \"Jsc [mA cm\\u22122]\": \"23.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"394.0\"}, {\"Refs.\": \"L. Sun, W. Wang, L. Hao, A. Raza, Y. Zhao, Z. Tang, G. Zhi, H. Yao, Ceram. Int. 2022, 48, 19891.\", \"PCE [%]\": \"4.9\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"Cu2ZnSn(S,Se)4\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.07\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"47.3\", \"Jsc [mA cm\\u22122]\": \"28.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"358.0\"}, {\"Refs.\": \"W. Xie, Q. Sun, Q. Yan, J. Wu, C. Zhang, Q. Zheng, Y. Lai, H. Deng, S. Cheng, Small 2022, 18, 2201347.\", \"PCE [%]\": \"10.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"Cu2ZnSn(S,Se)4\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.13\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.0\", \"Jsc [mA cm\\u22122]\": \"35.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"463.0\"}, {\"Refs.\": \"Q. Zhao, H. Shen, Y. Xu, K. Gao, D. Chen, Y. Li, ACS Appl. Energy Mater. 2022, 5, 3668.\", \"PCE [%]\": \"6.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"CZTSSe\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.59\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"48.0\", \"Jsc [mA cm\\u22122]\": \"22.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table15\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"601.0\"}, {\"Refs.\": \"D.-Y. Jung, Y.-R. Jeong, M. S. Mina, S.-E. Lee, E. Enkhbayar, J. Kim, Curr. Appl. Phys. 2022, 41, 66.\", \"PCE [%]\": \"11.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CIGSSe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"64.6\", \"Jsc [mA cm\\u22122]\": \"33.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"526.0\"}, {\"Refs.\": \"S. Pouladi, C. Favela, W. Wang, M. Moradnia, N.-I. Kim, S. Shervin, J. Chen, S. Sharma, G. Yang, M.-C. Nguyen, R. Choi, J. Kim, A. Fedorenko, B. Bogner, J. Bao, S. M. Hubbard, V. Selvamanickam, J.-H. Ryou, Sol. Energy Mater. Sol. Cells 2022, 243, 111791.\", \"PCE [%]\": \"13.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"GaAs\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.7\", \"Jsc [mA cm\\u22122]\": \"22.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"786.0\"}, {\"Refs.\": \"W. L. Rance, J. M. Burst, D. M. Meysing, C. A. Wolden, M. O. Reese, T. A. Gessert, W. K. Metzger, S. Garner, P. Cimo, T. M. Barnes, Appl. Phys. Lett. 2014, 104, 143903.\", \"PCE [%]\": \"14.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"CdTe\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.46\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.3\", \"Jsc [mA cm\\u22122]\": \"24.334\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table16\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"821.0\"}, {\"Refs.\": \"B. Tyagi, H. B. Lee, N. Kumar, W.-Y. Jin, K.-J. Ko, M. M. Ovhal, R. Sahani, H.-J. Chung, J. Seo, J.-W. Kang, Nano Energy 2022, 95, 106978.\", \"PCE [%]\": \"16.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"3.0\", \"Absorber\": \"Cs0.25FA0.75PbBr0.6I2.4\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.67\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"78.3\", \"Jsc [mA cm\\u22122]\": \"18.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1099.0\"}, {\"Refs.\": \"S. Seo, K. Akino, J.-S. Nam, A. Shawky, H.-S. Lin, H. Nagaya, E. I. Kauppinen, R. Xiang, Y. Matsuo, I. Jeon, S. Maruyama, Adv. Mater. Interfaces 2022, 9, 2101595.\", \"PCE [%]\": \"19.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"MAPbI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"73.4\", \"Jsc [mA cm\\u22122]\": \"23.2\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"S. Yoon, H. U. Ha, H.-J. Seok, H.-K. Kim, D.-W. Kang, Adv. Funct. Mater. 2022, 32, 2111760.\", \"PCE [%]\": \"17.8\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"9.0\", \"Absorber\": \"Cs0.13FA0.87PbBr0.39I2.61\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.63\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"82.7\", \"Jsc [mA cm\\u22122]\": \"19.3\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1120.0\"}, {\"Refs.\": \"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\", \"PCE [%]\": \"13.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"13.0\", \"Absorber\": \"Cs0.25FA0.75PbBr1.5I1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.1\", \"Jsc [mA cm\\u22122]\": \"13.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1298.0\"}, {\"Refs.\": \"S. Lie, A. Bruno, L. H. Wong, L. Etgar, ACS Appl. Mater. Interfaces 2022, 14, 11339.\", \"PCE [%]\": \"11.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"15.0\", \"Absorber\": \"Cs0.05FA0.775MA0.1615PbBr0.51I2.49\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"62.0\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1094.0\"}, {\"Refs.\": \"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\", \"PCE [%]\": \"8.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"23.0\", \"Absorber\": \"Cs0.25FA0.75PbBr1.5I1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.9\", \"Jsc [mA cm\\u22122]\": \"10.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1236.0\"}, {\"Refs.\": \"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"35.0\", \"Absorber\": \"Cs0.25FA0.75PbBr1.5I1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"72.3\", \"Jsc [mA cm\\u22122]\": \"12.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1289.0\"}, {\"Refs.\": \"J. C. Yu, B. Li, C. J. Dunn, J. Yan, B. T. Diroll, A. S. R. Chesman, J. J. Jasieniak, Adv. Sci. 2022, 9, 2201487.\", \"PCE [%]\": \"4.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"52.0\", \"Absorber\": \"Cs0.25FA0.75PbBr1.5I1.5\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.88\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"5.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table17\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1125.0\"}, {\"Refs.\": \"D. Han, S. Han, Z. Bu, Y. Deng, C. Liu, W. Guo, Sol. RRL 2022, 6, 2200441.\", \"PCE [%]\": \"12.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"8.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"D18-Cl:Y6:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.4\", \"Jsc [mA cm\\u22122]\": \"21.1\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"852.0\"}, {\"Refs.\": \"L. Zheng, M. Li, S. Dai, Y. Wu, Y. Cai, X. Zhu, S. Ma, D. Yun, J.-F. Li, J. Phys. Chem. C 2021, 125, 18623.\", \"PCE [%]\": \"13.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"19.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y7\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.2\", \"Jsc [mA cm\\u22122]\": \"23.4\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"830.0\"}, {\"Refs.\": \"W. Liu, S. Sun, L. Zhou, Y. Cui, W. Zhang, J. Hou, F. Liu, S. Xu, X. Zhu, Angew. Chem., Int. Ed. 2022, 61, 202116111.\", \"PCE [%]\": \"14.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6:SN3\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.37\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.3\", \"Jsc [mA cm\\u22122]\": \"23.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"820.0\"}, {\"Refs.\": \"S. Liu, H. Li, X. Wu, D. Chen, L. Zhang, X. Meng, L. Tan, X. Hu, Y. Chen, Adv. Mater. 2022, 34, 2201604.\", \"PCE [%]\": \"14.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6/ICBA:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.7\", \"Jsc [mA cm\\u22122]\": \"22.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"860.0\"}, {\"Refs.\": \"W. Liu, S. Sun, S. Xu, H. Zhang, Y. Zheng, Z. Wei, X. Zhu, Adv. Mater. 2022, 34, 2200337.\", \"PCE [%]\": \"11.6\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"20.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"BTB7-Th:ATT-9\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.23\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"68.2\", \"Jsc [mA cm\\u22122]\": \"25.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"661.0\"}, {\"Refs.\": \"X. Yuan, R. Sun, Y. Wu, T. Wang, Y. Wang, W. Wang, Y. Yu, J. Guo, Q. Wu, J. Min, Adv. Funct. Mater. 2022, 32, 2200107.\", \"PCE [%]\": \"16.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"21.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6-Ir1:BTP-eC9:PC71BM\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"76.1\", \"Jsc [mA cm\\u22122]\": \"24.6\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"859.0\"}, {\"Refs.\": \"H. I. Jeong, S. Biswas, S. C. Yoon, S.-J. Ko, H. Kim, H. Choi, Adv. Energy Mater. 2021, 11, 2102397.\", \"PCE [%]\": \"12.1\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.6\", \"Jsc [mA cm\\u22122]\": \"23.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"760.0\"}, {\"Refs.\": \"J. Jing, S. Dong, K. Zhang, Z. Zhou, Q. Xue, Y. Song, Z. Du, M. Ren, F. Huang, Adv. Energy Mater. 2022, 12, 2200453.\", \"PCE [%]\": \"11.3\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"28.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6-BO\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"70.3\", \"Jsc [mA cm\\u22122]\": \"19.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"816.0\"}, {\"Refs.\": \"X. Huang, L. Zhang, Y. Cheng, J. Oh, C. Li, B. Huang, L. Zhao, J. Deng, Y. Zhang, Z. Liu, F. Wu, X. Hu, C. Yang, L. Chen, Y. Chen, Adv. Funct. Mater. 2022, 32, 2108634.\", \"PCE [%]\": \"12.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"31.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PCE10-BDT2F-0.8:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"69.5\", \"Jsc [mA cm\\u22122]\": \"22.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"758.0\"}, {\"Refs.\": \"D. Wang, Y. Li, G. Zhou, E. Gu, R. Xia, B. Yan, J. Yao, H. Zhu, X. Lu, H.-L. Yip, H. Chen, C.-Z. Li, Energy Environ. Sci. 2022, 15, 2629.\", \"PCE [%]\": \"11.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"32.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:m-BTP-PhC6:BO-Cl\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.42\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.6\", \"Jsc [mA cm\\u22122]\": \"17.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"849.0\"}, {\"Refs.\": \"S. Guan, Y. Li, K. Yan, W. Fu, L. Zuo, H. Chen, Adv. Mater. 2022, 34, 2205844.\", \"PCE [%]\": \"13.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"39.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PBDB-TF:L8-BO:BTP-eC9\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.41\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"80.3\", \"Jsc [mA cm\\u22122]\": \"19.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"849.0\"}, {\"Refs.\": \"H. I. Jeong, S. Biswas, S. C. Yoon, S.-J. Ko, H. Kim, H. Choi, Adv. Energy Mater. 2021, 11, 2102397.\", \"PCE [%]\": \"9.7\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"25.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:Y6\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.43\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"63.0\", \"Jsc [mA cm\\u22122]\": \"20.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"770.0\"}, {\"Refs.\": \"X. Liu, Z. Zhong, R. Zhu, J. Yu, G. Li, Joule 2022, 6, 1918.\", \"PCE [%]\": \"11.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"47.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"PM6:BTP-eC9:L8-BO\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.39\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"74.5\", \"Jsc [mA cm\\u22122]\": \"18.0\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table18\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"854.0\"}, {\"Refs.\": \"X. Xie, Y. Zhang, Y. Ren, L. He, Y. Yuan, J. Zhang, P. Wang, J. Phys. Chem. C 2022, 126, 11007.\", \"PCE [%]\": \"11.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"5.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.8\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"75.2\", \"Jsc [mA cm\\u22122]\": \"16.8\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"C268 + Y1\", \"Table\": \"ver3_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"871.0\"}, {\"Refs.\": \"A. K. Bharwal, L. Manceriu, C. Olivier, A. Mahmoud, C. Iojoiu, T. Toupance, C. M. Ruiz, M. Pasquinelli, D. Duch\\u00e9, J.-J. Simon, C. Henrist, F. Alloin, Chem. Eng. J. 2022, 446, 136777.\", \"PCE [%]\": \"5.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"10.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.81\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"60.7\", \"Jsc [mA cm\\u22122]\": \"11.7\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"N719\", \"Table\": \"ver3_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"710.0\"}, {\"Refs.\": \"F. Odobel, T. Baron, W. Naim, I. Nikolinakos, B. Andrin, Y. Pellegrin, D. Jacquemin, S. Haacke, F. Sauvage, Angew. Chem., Int. Ed. 2022, 61, 202207459.\", \"PCE [%]\": \"2.5\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"75.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"56.2\", \"Jsc [mA cm\\u22122]\": \"10.9\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"TB207\", \"Table\": \"ver3_table19\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"408.0\"}, {\"Refs.\": \"C. Yang, M. Moemeni, M. Bates, W. Sheng, B. Borhan, R. R. Lunt, Adv. Opt. Mater. 2020, 8, 1901536.\", \"PCE [%]\": \"1.2\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"74.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.5\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"81.3\", \"Jsc [mA cm\\u22122]\": \"1.5\", \"Luminophore(s)/absorber\": \"COi8DFIC/GaAs\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table22\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"990.0\"}, {\"Refs.\": \"C. Yang, W. Sheng, M. Moemeni, M. Bates, C. K. Herrera, B. Borhan, R. R. Lunt, Adv. Energy Mater. 2021, 11, 2003581.\", \"PCE [%]\": \"3.0\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"75.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.64\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"77.7\", \"Jsc [mA cm\\u22122]\": \"3.8\", \"Luminophore(s)/absorber\": \"Cs2Mo6I8(CF3CF2COO)6:BODIPY/GaAs\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table22\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"1020.0\"}, {\"Refs.\": \"Y. Zhao, R. R. Lunt, Adv. Energy Mater. 2013, 3, 1143.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"84.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.11\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"65.1\", \"Jsc [mA cm\\u22122]\": \"1.3\", \"Luminophore(s)/absorber\": \"(TBA)2Mo6Cl14/Si\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table22\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"520.0\"}, {\"Refs.\": \"Y. Zhao, G. A. Meek, B. G. Levine, R. R. Lunt, Adv. Opt. Mater. 2014, 2, 606.\", \"PCE [%]\": \"0.4\", \"0 h PCE [%]\": \"\", \"200 h PCE [%]\": \"\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"\", \"AVT [%]\": \"86.0\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"\", \"E1000h [Wh cm\\u22122]\": \"\", \"Eg [eV]\": \"1.52\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"66.7\", \"Jsc [mA cm\\u22122]\": \"1.2\", \"Luminophore(s)/absorber\": \"Cy7-NHS/Si\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table22\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"500.0\"}, {\"Refs.\": \"['J. Sanchez-Diaz, R. S. S\\u00e1nchez, S. Masi, M. Kre\\u0109marov\\u00e1, A. O. Alvarez, E. M. Barea, J. Rodriguez-Romero, V. S. Chirvony, J. F. S\\u00e1nchez-Royo, J. P. Martinez-Pastor, I. Mora-Ser\\u00f3, Joule 2022, 6, 861.', 'J. Sanchez-Diaz, R. S. S\\u00e1nchez, S. Masi, M. Kre\\u0109marov\\u00e1, A. O. Alvarez, E. M. Barea, J. Rodriguez-Romero, V. S. Chirvony, J. F. S\\u00e1nchez-Royo, J. P. Martinez-Pastor, I. Mora-Ser\\u00f3, https://emerging-pv.org/wp-content/uploads/2022/06/Add_SI_Stability-PSC_Joule.2022.02.014.pdf (accessed: June 2022).']\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"9.4\", \"200 h PCE [%]\": \"9.4\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"9.2\", \"AVT [%]\": \"\", \"Absorber\": \"FASnI3+NaBH4+DipI\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, N2, 70 \\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"1.9\", \"E1000h [Wh cm\\u22122]\": \"9.3\", \"Eg [eV]\": \"1.4\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"T. Wu, X. Liu, X. Luo, H. Segawa, G. Tong, Y. Zhang, L. K. Ono, Y. Qi, L. Han, Nano-Micro Lett. 2022, 14, 99.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"13.8\", \"200 h PCE [%]\": \"14.1\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"13.0\", \"AVT [%]\": \"\", \"Absorber\": \"FASnI3\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, air\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"2.8\", \"E1000h [Wh cm\\u22122]\": \"13.6\", \"Eg [eV]\": \"1.45\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"F. Zhang, Y. Park So, C. Yao, H. Lu, P. Dunfield Sean, C. Xiao, S. Uli\\u010dn\\u00e1, X. Zhao, L. Du Hill, X. Chen, X. Wang, E. Mundt Laura, H. Stone Kevin, T. Schelhas Laura, G. Teeter, S. Parkin, L. Ratcliff Erin, Y.-L. Loo, J. Berry Joseph, C. Beard Matthew, Y. Yan, W. Larson Bryon, K. Zhu, Science 2022, 375, 71.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"23.1\", \"200 h PCE [%]\": \"22.7\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"20.7\", \"AVT [%]\": \"\", \"Absorber\": \"FA0.97MA0.03PbI2.91Br0.09\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, N2, 40 \\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.6\", \"E1000h [Wh cm\\u22122]\": \"22.0\", \"Eg [eV]\": \"1.53\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"X. Li, W. Zhang, X. Guo, C. Lu, J. Wei, J. Fang, Science 2022, 375, 434.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"19.8\", \"200 h PCE [%]\": \"20.6\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"17.7\", \"AVT [%]\": \"\", \"Absorber\": \"FA0.95MA0.05PbBr0.15I2.85\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, w-LED, air, 55 \\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.1\", \"E1000h [Wh cm\\u22122]\": \"19.1\", \"Eg [eV]\": \"1.57\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"J. Peng, F. Kremer, D. Walter, Y. Wu, Y. Ji, J. Xiang, W. Liu, T. Duong, H. Shen, T. Lu, F. Brink, D. Zhong, L. Li, O. Lee Cheong Lem, Y. Liu, K. J. Weber, T. P. White, K. R. Catchpole, Nature 2022, 601, 573.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"23.1\", \"200 h PCE [%]\": \"22.9\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"Cs0.05FA0.9MA0.05\\u00a0Pb Br0.26I2.74\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, N2\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.6\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"Q. Zhou, C. Cai, Q. Xiong, Z. Zhang, J. Xu, L. Liang, S. Wang, W. Sun, Z. Yuan, P. Gao, Adv. Energy Mater. 2022, 12, 2201243.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"23.6\", \"200 h PCE [%]\": \"20.2\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \" \", \"AVT [%]\": \"\", \"Absorber\": \"FA0.92MA0.08PbBr0.24I2.76\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, air, 50% RH\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"4.4\", \"E1000h [Wh cm\\u22122]\": \" \", \"Eg [eV]\": \"1.58\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"B. Fan, J. Xiong, Y. Zhang, C. Gong, F. Li, X. Meng, X. Hu, Z. Yuan, F. Wang, Y. Chen, Adv. Mater. 2022, 34, 2201840.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"19.6\", \"200 h PCE [%]\": \"18.4\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"16.3\", \"AVT [%]\": \"\", \"Absorber\": \"CsFAMAPbBrI\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"\", \"Comments\": \"MPP, AM1.5G, air, 40% RH, 30 \\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"3.8\", \"E1000h [Wh cm\\u22122]\": \"17.4\", \"Eg [eV]\": \"1.6\", \"Top Eg [eV]\": \"\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table23\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"\", \"Voc [mV]\": \"\"}, {\"Refs.\": \"R. Lin, J. Xu, M. Wei, Y. Wang, Z. Qin, Z. Liu, J. Wu, K. Xiao, B. Chen, S. M. Park, G. Chen, H. R. Atapattu, K. R. Graham, J. Xu, J. Zhu, L. Li, C. Zhang, E. H. Sargent, H. Tan, Nature 2022, 603, 73.\", \"PCE [%]\": \"\", \"0 h PCE [%]\": \"25.6\", \"200 h PCE [%]\": \"26.4\", \"100 h PCE [%]\": \"\", \"1000 h PCE [%]\": \"17.8\", \"AVT [%]\": \"\", \"Absorber\": \"\", \"Absorber blend\": \"\", \"Absorber material\": \"\", \"Absorber material/technology\": \"\", \"Absorber perovskite\": \"\", \"Absorber/technology\": \"\", \"Active material\": \"\", \"Bottom Eg [eV]\": \"1.25\", \"Bottom absorber\": \"\", \"Bottom absorber material\": \"FA0.8Cs0.2Pb(I0.62Br0.38)3\", \"Comments\": \"MPP, AM1.5G, air 30\\u201350% RH, 35 \\u00b0C\", \"Dye sensitizer\": \"\", \"E200h [Wh cm\\u22122]\": \"5.2\", \"E1000h [Wh cm\\u22122]\": \"23.5\", \"Eg [eV]\": \"\", \"Top Eg [eV]\": \"1.8\", \"Eg,bottom [eV]\": \"\", \"Eg,middle, Eg,top [eV]\": \"\", \"FF [%]\": \"\", \"Jsc [mA cm\\u22122]\": \"\", \"Luminophore(s)/absorber\": \"\", \"Middle, top absorber material(s)\": \"\", \"Middle, top absorber(s)\": \"\", \"Sensitizing dye\": \"\", \"Table\": \"ver3_table26\", \"Top absorber\": \"\", \"Top absorber material(s)\": \"FA0.7MA0.3Pb0.5Sn0.5I3\", \"Voc [mV]\": \"\"}]"
  },
  {
    "path": "dataset/Experimental thermoelectric properties 2013/MRL.csv",
    "content": "doi,Electrical resistivity (Ωcm),Seebeck coefficient (μCV/K),ZT (thermoelectric figure of merit) ,formula,synthesis,form,temperature,Thermal conductivity (W/mK),Average atomic mass (g/mol),Scarcity (wt fraction/abundance),HHIP (Herfindahl?Hirschman Index for elemental production),HHIR (Herfindahl?Hirschman Index for elemental reserves),Unit cell volume (ų),Average atomic volume (ų),Atoms per unit cell,Electrical conductivity (Ω⁻¹ cm⁻¹),Power Factor (W/(K²m)),S² (μV/K)²,Electronic fraction of thermal conductivity (ϰₑ/ϰ)\r\n10.1002/adfm.201000970,0.457,470,0.01,Ca5Al2Sb6,\"solid state reaction, Ar\",polycrystalline,300,1.54,75.76,3709000,6736,2896,770.68,29.642,26,2.188,4.83E-05,221000,0.00104\r\n10.1002/adfm.201000970,0.033,193,0.03,Ca4.95Na0.05Al2Sb6,\"solid state reaction, Ar\",polycrystalline,300,1.49,75.7,3712000,6735,2896,770.68,29.642,26,30.1,0.000112,37200,0.015\r\n10.1002/adfm.201000970,0.00506,143,0.12,Ca4.75Na0.25Al2Sb6,\"solid state reaction, Ar\",polycrystalline,300,1.45,75.43,3725000,6732,2896,770.68,29.642,26,198,0.000402,20400,0.1\r\n10.1002/adfm.201000970,0.409,463,0.02,Ca5Al2Sb6,\"solid state reaction, Ar\",polycrystalline,400,1.23,75.76,3709000,6736,2896,770.68,29.642,26,2.445,5.24E-05,214000,0.00194\r\n10.1002/adfm.201000970,0.022,220,0.09,Ca4.95Na0.05Al2Sb6,\"solid state reaction, Ar\",polycrystalline,400,1.2,75.7,3712000,6735,2896,770.68,29.642,26,44.6,0.000216,48400,0.036\r\n10.1002/adfm.201000970,0.00544,161,0.19,Ca4.75Na0.25Al2Sb6,\"solid state reaction, Ar\",polycrystalline,400,1.16,75.43,3725000,6732,2896,770.68,29.642,26,184,0.000476,25900,0.155\r\n10.1002/adfm.201000970,0.235,390,0.05,Ca5Al2Sb6,\"solid state reaction, Ar\",polycrystalline,700,0.764,75.76,3709000,6736,2896,770.68,29.642,26,4.257,6.48E-05,152000,0.00952\r\n10.1002/adfm.201000970,0.018,262,0.26,Ca4.95Na0.05Al2Sb6,\"solid state reaction, Ar\",polycrystalline,700,0.833,75.7,3712000,6735,2896,770.68,29.642,26,55.2,0.000378,68500,0.113\r\n10.1002/adfm.201000970,0.00733,201,0.39,Ca4.75Na0.25Al2Sb6,\"solid state reaction, Ar\",polycrystalline,700,0.82,75.43,3725000,6732,2896,770.68,29.642,26,136,0.00055,40300,0.284\r\n10.1002/adfm.201000970,0.00939,207,0.46,Ca4.75Na0.25Al2Sb6,\"solid state reaction, Ar\",polycrystalline,1000,0.703,75.43,3725000,6732,2896,770.68,29.642,26,106,0.000456,42800,0.37\r\n10.1002/chin.199644003,0.165,-25,0.000114,K1Bi6.33S10,\"solid state reaction, vacuum\",polycrystalline,300,1.3,97.09,46250000,4345,5070,1204.18,33.449,36,6.061,3.79E-07,625,0.00341\r\n10.1002/chin.200318015,2.919,-752,0.00582,Nd2Cu1O4,\"solid state reaction, air\",polycrystalline,300,29.6,59.43,21000,6889,2479,189.28,13.52,14,0.343,1.94E-05,566000,8.47E-06\r\n10.1002/chin.200318015,0.059,-249,0.03,Nd2Cu0.98Ni0.02O4,\"solid state reaction, air\",polycrystalline,300,9.811,59.42,20980,6888,2480,189.28,13.52,14,16.8,0.000105,62200,0.00126\r\n10.1002/chin.200318015,0.19,-343,0.02,Nd2Cu0.98Zn0.02O4,\"solid state reaction, air\",polycrystalline,300,17.1,59.44,21000,6888,2481,189.28,13.52,14,5.269,6.21E-05,118000,0.000226\r\n10.1002/chin.200318015,2.162,-618,0.00708,Nd2Cu1O4,\"solid state reaction, air\",polycrystalline,400,13.7,59.43,21000,6889,2479,189.28,13.52,14,0.463,1.77E-05,382000,3.30E-05\r\n10.1002/chin.200318015,0.038,-183,0.03,Nd2Cu0.98Ni0.02O4,\"solid state reaction, air\",polycrystalline,400,8.03,59.42,20980,6888,2480,189.28,13.52,14,26.1,8.72E-05,33400,0.00318\r\n10.1002/chin.200318015,0.141,-294,0.02,Nd2Cu0.98Zn0.02O4,\"solid state reaction, air\",polycrystalline,400,11.1,59.44,21000,6888,2481,189.28,13.52,14,7.115,6.17E-05,86700,0.000626\r\n10.1002/chin.200318015,0.024,-100,0.03,Nd2Cu1O4,\"solid state reaction, air\",polycrystalline,700,4.19,59.43,21000,6889,2479,189.28,13.52,14,41,4.08E-05,9940,0.017\r\n10.1002/chin.200318015,0.022,-99,0.03,Nd2Cu0.98Ni0.02O4,\"solid state reaction, air\",polycrystalline,700,5.25,59.42,20980,6888,2480,189.28,13.52,14,46.3,4.49E-05,9700,0.015\r\n10.1002/chin.200318015,0.076,-176,0.03,Nd2Cu0.98Zn0.02O4,\"solid state reaction, air\",polycrystalline,700,5.22,59.44,21000,6888,2481,189.28,13.52,14,13.1,4.04E-05,30800,0.00429\r\n10.1002/chin.200318015,0.00158,26,0.04,Nd2Cu1O4,\"solid state reaction, air\",polycrystalline,1000,3.94,59.43,21000,6889,2479,189.28,13.52,14,631,4.35E-05,690,0.391\r\n10.1002/chin.200318015,0.023,-83,0.03,Nd2Cu0.98Ni0.02O4,\"solid state reaction, air\",polycrystalline,1000,3.902,59.42,20980,6888,2480,189.28,13.52,14,43.6,2.98E-05,6830,0.027\r\n10.1002/chin.200318015,0.037,-64,0.01,Nd2Cu0.98Zn0.02O4,\"solid state reaction, air\",polycrystalline,1000,3.63,59.44,21000,6888,2481,189.28,13.52,14,26.9,1.09E-05,4060,0.018\r\n10.1006/jssc.1995.1384,0.00371,-83,0.06,Ca0.9Bi0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,3.591,31.98,7688000,2260,1887,213.57,10.678,20,270,0.000184,6830,0.055\r\n10.1006/jssc.1995.1384,0.00729,-49,0.00995,Ca0.9Ce0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,30.6,1819,2506,1440,215.14,10.757,20,137,3.32E-05,2420,\r\n10.1006/jssc.1995.1384,0.018,-87,0.01,Ca0.9Y0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,29.58,2323,2287,1352,215.14,10.757,20,56.3,4.23E-05,7510,\r\n10.1006/jssc.1995.1384,0.00863,-102,0.04,Ca0.9Sm0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,30.81,15330,2553,1451,210.39,10.519,20,116,0.000121,10400,\r\n10.1006/jssc.1995.1384,0.462,-70,0.000317,Ca0.9Sb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,30.24,403100,2295,1442,210.39,10.519,20,2.164,1.06E-06,4890,\r\n10.1006/jssc.1995.1384,0.00796,-93,0.03,Ca0.9La0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,30.58,2861,2501,1438,212.03,10.602,20,126,0.000109,8650,\r\n10.1006/jssc.1995.1384,0.045,-274,0.05,Ca0.9Pb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,31.95,11170,1922,1336,212.03,10.602,20,22.5,0.000169,75200,\r\n10.1006/jssc.1995.1384,0.215,-348,0.02,Ca0.9In0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,30.1,372600,1921,1325,212.03,10.602,20,4.651,5.65E-05,121000,\r\n10.1006/jssc.1995.1384,2.198,-284,0.0011,Ca0.9Sn0.1Mn1O3,\"solid state reaction, air\",polycrystalline,300,,30.18,35350,1866,1298,212.03,10.602,20,0.455,3.67E-06,80600,\r\n10.1006/jssc.1995.1384,6.975,-477,0.000977,Ca1Mn1O3,\"solid state reaction, air\",polycrystalline,300,2.99,28.6,398,1861,1276,206.97,10.348,20,0.143,3.26E-06,227000,3.51E-05\r\n10.1006/jssc.1995.1384,0.004,-101,0.1,Ca0.9Bi0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,3.147,31.98,7688000,2260,1887,213.57,10.678,20,250,0.000254,10200,0.078\r\n10.1006/jssc.1995.1384,0.00645,-55,0.02,Ca0.9Ce0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,30.6,1819,2506,1440,215.14,10.757,20,155,4.76E-05,3070,\r\n10.1006/jssc.1995.1384,0.015,-91,0.02,Ca0.9Y0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,29.58,2323,2287,1352,215.14,10.757,20,66.1,5.50E-05,8320,\r\n10.1006/jssc.1995.1384,0.00747,-106,0.06,Ca0.9Sm0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,30.81,15330,2553,1451,210.39,10.519,20,134,0.00015,11200,\r\n10.1006/jssc.1995.1384,0.115,-71,0.00175,Ca0.9Sb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,30.24,403100,2295,1442,210.39,10.519,20,8.674,4.36E-06,5030,\r\n10.1006/jssc.1995.1384,0.00699,-98,0.06,Ca0.9La0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,30.58,2861,2501,1438,212.03,10.602,20,143,0.000139,9680,\r\n10.1006/jssc.1995.1384,0.052,-266,0.05,Ca0.9Pb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,31.95,11170,1922,1336,212.03,10.602,20,19.1,0.000135,70800,\r\n10.1006/jssc.1995.1384,0.205,-357,0.02,Ca0.9In0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,30.1,372600,1921,1325,212.03,10.602,20,4.887,6.21E-05,127000,\r\n10.1006/jssc.1995.1384,2.302,-282,0.00138,Ca0.9Sn0.1Mn1O3,\"solid state reaction, air\",polycrystalline,400,,30.18,35350,1866,1298,212.03,10.602,20,0.434,3.45E-06,79400,\r\n10.1006/jssc.1995.1384,2.87,-461,0.00296,Ca1Mn1O3,\"solid state reaction, air\",polycrystalline,400,3.178,28.6,398,1861,1276,206.97,10.348,20,0.348,7.41E-06,213000,0.000107\r\n10.1006/jssc.1995.1384,0.005,-120,0.2,Ca0.9Bi0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,2.214,31.98,7688000,2260,1887,213.57,10.678,20,200,0.000287,14300,0.154\r\n10.1006/jssc.1995.1384,0.00666,-60,0.04,Ca0.9Ce0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,30.6,1819,2506,1440,215.14,10.757,20,150,5.40E-05,3600,\r\n10.1006/jssc.1995.1384,0.016,-103,0.05,Ca0.9Y0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,29.58,2323,2287,1352,215.14,10.757,20,63.1,6.64E-05,10500,\r\n10.1006/jssc.1995.1384,0.00788,-147,0.19,Ca0.9Sm0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,30.81,15330,2553,1451,210.39,10.519,20,127,0.000273,21500,\r\n10.1006/jssc.1995.1384,0.067,-81,0.00686,Ca0.9Sb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,30.24,403100,2295,1442,210.39,10.519,20,14.9,9.80E-06,6570,\r\n10.1006/jssc.1995.1384,0.00855,-117,0.11,Ca0.9La0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,30.58,2861,2501,1438,212.03,10.602,20,117,0.00016,13700,\r\n10.1006/jssc.1995.1384,0.061,-277,0.09,Ca0.9Pb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,31.95,11170,1922,1336,212.03,10.602,20,16.5,0.000127,76800,\r\n10.1006/jssc.1995.1384,0.231,-411,0.05,Ca0.9In0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,30.1,372600,1921,1325,212.03,10.602,20,4.333,7.32E-05,169000,\r\n10.1006/jssc.1995.1384,2.082,-255,0.00219,Ca0.9Sn0.1Mn1O3,\"solid state reaction, air\",polycrystalline,700,,30.18,35350,1866,1298,212.03,10.602,20,0.48,3.13E-06,65100,\r\n10.1006/jssc.1995.1384,0.485,-332,0.02,Ca1Mn1O3,\"solid state reaction, air\",polycrystalline,700,3.311,28.6,398,1861,1276,206.97,10.348,20,2.061,2.27E-05,110000,0.00106\r\n10.1006/jssc.1995.1384,0.00519,-96,0.18,Ca0.9Bi0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,1.841,31.98,7688000,2260,1887,213.57,10.678,20,193,0.000178,9220,0.255\r\n10.1006/jssc.1995.1384,0.00789,-80,0.08,Ca0.9Ce0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,30.6,1819,2506,1440,215.14,10.757,20,127,8.21E-05,6480,\r\n10.1006/jssc.1995.1384,0.018,-108,0.07,Ca0.9Y0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,29.58,2323,2287,1352,215.14,10.757,20,56.8,6.57E-05,11600,\r\n10.1006/jssc.1995.1384,0.00783,-123,0.19,Ca0.9Sm0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,30.81,15330,2553,1451,210.39,10.519,20,128,0.000192,15100,\r\n10.1006/jssc.1995.1384,0.064,-70,0.00765,Ca0.9Sb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,30.24,403100,2295,1442,210.39,10.519,20,15.6,7.65E-06,4920,\r\n10.1006/jssc.1995.1384,0.01,-88,0.08,Ca0.9La0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,30.58,2861,2501,1438,212.03,10.602,20,97.2,7.60E-05,7820,\r\n10.1006/jssc.1995.1384,0.047,-115,0.03,Ca0.9Pb0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,31.95,11170,1922,1336,212.03,10.602,20,21.4,2.81E-05,13200,\r\n10.1006/jssc.1995.1384,0.173,-235,0.03,Ca0.9In0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,30.1,372600,1921,1325,212.03,10.602,20,5.766,3.18E-05,55100,\r\n10.1006/jssc.1995.1384,0.479,-145,0.00442,Ca0.9Sn0.1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,30.18,35350,1866,1298,212.03,10.602,20,2.089,4.42E-06,21200,\r\n10.1006/jssc.1995.1384,0.087,-193,0.04,Ca1Mn1O3,\"solid state reaction, air\",polycrystalline,1000,3.445,28.6,398,1861,1276,206.97,10.348,20,11.4,4.25E-05,37200,0.0081\r\n10.1007/978-3-540-88201-5_24,0.00962,-50,0.00771,Sr1Dy0.08Ti0.92O3,\"solid state reaction, air\",polycrystalline,300,4.195,38.53,13120,2920,2055,60.64,12.128,5,104,2.57E-05,2470,0.018\r\n10.1007/978-3-540-88201-5_24,0.0026,-32,0.01,Sr1Nd0.17Ti0.83O3,\"solid state reaction, air\",polycrystalline,300,6.19,39.97,4528,3337,2128,60.64,12.128,5,385,4.07E-05,1060,0.046\r\n10.1007/978-3-540-88201-5_24,0.00184,-34,0.02,Sr1Nd0.2Ti0.8O3,\"solid state reaction, air\",polycrystalline,300,5.53,40.55,5035,3484,2153,60.64,12.128,5,544,6.44E-05,1180,0.072\r\n10.1007/978-3-540-88201-5_24,0.00225,-23,0.00682,Sr1Nd0.24Ti0.76O3,\"solid state reaction, air\",polycrystalline,300,5.98,41.32,5689,3673,2186,60.64,12.128,5,445,2.27E-05,511,0.054\r\n10.1007/978-3-540-88201-5_24,0.004,-70,0.05,Sr1Dy0.08Ti0.92O3,\"solid state reaction, air\",polycrystalline,400,3.74,38.53,13120,2920,2055,60.64,12.128,5,250,0.000124,4970,0.065\r\n10.1007/978-3-540-88201-5_24,0.00193,-42,0.04,Sr1Nd0.17Ti0.83O3,\"solid state reaction, air\",polycrystalline,400,5.35,39.97,4528,3337,2128,60.64,12.128,5,519,9.24E-05,1780,0.095\r\n10.1007/978-3-540-88201-5_24,0.00147,-45,0.05,Sr1Nd0.2Ti0.8O3,\"solid state reaction, air\",polycrystalline,400,4.83,40.55,5035,3484,2153,60.64,12.128,5,678,0.000137,2020,0.137\r\n10.1007/978-3-540-88201-5_24,0.00181,-32,0.02,Sr1Nd0.24Ti0.76O3,\"solid state reaction, air\",polycrystalline,400,5.29,41.32,5689,3673,2186,60.64,12.128,5,553,5.49E-05,992,0.102\r\n10.1007/978-3-540-88201-5_24,0.00459,-147,0.33,Sr1Dy0.08Ti0.92O3,\"solid state reaction, air\",polycrystalline,700,3.17,38.53,13120,2920,2055,60.64,12.128,5,218,0.000471,21600,0.117\r\n10.1007/978-3-540-88201-5_24,0.00227,-96,0.28,Sr1Nd0.17Ti0.83O3,\"solid state reaction, air\",polycrystalline,700,3.87,39.97,4528,3337,2128,60.64,12.128,5,441,0.000406,9220,0.194\r\n10.1007/978-3-540-88201-5_24,0.00195,-94,0.32,Sr1Nd0.2Ti0.8O3,\"solid state reaction, air\",polycrystalline,700,3.45,40.55,5035,3484,2153,60.64,12.128,5,512,0.000456,8910,0.253\r\n10.1007/978-3-540-88201-5_24,0.00186,-81,0.24,Sr1Nd0.24Ti0.76O3,\"solid state reaction, air\",polycrystalline,700,3.76,41.32,5689,3673,2186,60.64,12.128,5,537,0.00035,6510,0.244\r\n10.1007/978-3-540-88201-5_24,0.00833,-192,0.44,Sr1Dy0.08Ti0.92O3,\"solid state reaction, air\",polycrystalline,1000,2.97,38.53,13120,2920,2055,60.64,12.128,5,120,0.000441,36700,0.099\r\n10.1007/978-3-540-88201-5_24,0.00418,-142,0.48,Sr1Nd0.17Ti0.83O3,\"solid state reaction, air\",polycrystalline,1000,3.397,39.97,4528,3337,2128,60.64,12.128,5,239,0.000481,20100,0.172\r\n10.1007/978-3-540-88201-5_24,0.00395,-140,0.5,Sr1Nd0.2Ti0.8O3,\"solid state reaction, air\",polycrystalline,1000,3.197,40.55,5035,3484,2153,60.64,12.128,5,253,0.000496,19600,0.193\r\n10.1007/978-3-540-88201-5_24,0.00319,-124,0.48,Sr1Nd0.24Ti0.76O3,\"solid state reaction, air\",polycrystalline,1000,3.22,41.32,5689,3673,2186,60.64,12.128,5,313,0.000481,15400,0.237\r\n10.1007/s10854-011-0574-8,1400,98,2.05E-07,W1O3,Solid state reaction,polycrystalline,300,,57.96,674900,5639,3511,422.94,13.217,32,0.000713,6.83E-10,9590,\r\n10.1007/s10854-011-0574-8,1250,93,2.06E-07,W0.99O2.97Co0.02O0.03,Solid state reaction,polycrystalline,300,,57.65,670200,5615,3500,422.94,13.217,32,0.000802,6.88E-10,8570,\r\n10.1007/s10854-011-0574-8,114,103,2.79E-06,W0.95O2.95Co0.1O0.15,Solid state reaction,polycrystalline,300,,55.45,646800,5484,3437,422.94,13.217,32,0.00873,9.31E-09,10700,\r\n10.1007/s10854-011-0574-8,561,104,5.77E-07,W0.9O2.7Co0.2O0.3,Solid state reaction,polycrystalline,300,,54.94,627100,5394,3402,422.94,13.217,32,0.00178,1.92E-09,10800,\r\n10.1007/s10854-011-0574-8,810,108,5.72E-07,W1O3,Solid state reaction,polycrystalline,400,,57.96,674900,5639,3511,422.94,13.217,32,0.00123,1.43E-09,11600,\r\n10.1007/s10854-011-0574-8,708,97,5.32E-07,W0.99O2.97Co0.02O0.03,Solid state reaction,polycrystalline,400,,57.65,670200,5615,3500,422.94,13.217,32,0.00141,1.33E-09,9420,\r\n10.1007/s10854-011-0574-8,99.4,106,4.52E-06,W0.95O2.95Co0.1O0.15,Solid state reaction,polycrystalline,400,,55.45,646800,5484,3437,422.94,13.217,32,0.01,1.13E-08,11200,\r\n10.1007/s10854-011-0574-8,176,106,2.54E-06,W0.9O2.7Co0.2O0.3,Solid state reaction,polycrystalline,400,,54.94,627100,5394,3402,422.94,13.217,32,0.00569,6.34E-09,11100,\r\n10.1007/s10854-011-0574-8,108,125,1.01E-05,W1O3,Solid state reaction,polycrystalline,700,,57.96,674900,5639,3511,422.94,13.217,32,0.00922,1.44E-08,15600,\r\n10.1007/s10854-011-0574-8,86,114,1.05E-05,W0.99O2.97Co0.02O0.03,Solid state reaction,polycrystalline,700,,57.65,670200,5615,3500,422.94,13.217,32,0.012,1.50E-08,12900,\r\n10.1007/s10854-011-0574-8,20.2,120,4.99E-05,W0.95O2.95Co0.1O0.15,Solid state reaction,polycrystalline,700,,55.45,646800,5484,3437,422.94,13.217,32,0.049,7.13E-08,14400,\r\n10.1007/s10854-011-0574-8,52.1,122,1.99E-05,W0.9O2.7Co0.2O0.3,Solid state reaction,polycrystalline,700,,54.94,627100,5394,3402,422.94,13.217,32,0.019,2.84E-08,14800,\r\n10.1007/s10854-011-0574-8,64.9,161,3.99E-05,W1O3,Solid state reaction,polycrystalline,1000,,57.96,674900,5639,3511,422.94,13.217,32,0.015,3.99E-08,25900,\r\n10.1007/s10854-011-0574-8,36.4,114,3.56E-05,W0.99O2.97Co0.02O0.03,Solid state reaction,polycrystalline,1000,,57.65,670200,5615,3500,422.94,13.217,32,0.027,3.56E-08,13000,\r\n10.1007/s10854-011-0574-8,15.9,126,9.93E-05,W0.95O2.95Co0.1O0.15,Solid state reaction,polycrystalline,1000,,55.45,646800,5484,3437,422.94,13.217,32,0.063,9.93E-08,15800,\r\n10.1007/s10854-011-0574-8,35.7,124,4.32E-05,W0.9O2.7Co0.2O0.3,Solid state reaction,polycrystalline,1000,,54.94,627100,5394,3402,422.94,13.217,32,0.028,4.32E-08,15400,\r\n10.1007/s11664-009-0735-1,0.00152,-83,0.14,Mg2Si0.98Bi0.02,\"solid state reaction, He/H2\",polycrystalline,300,7.13,26.77,3061000,5072,957.2,258.55,21.546,12,658,0.000452,6870,0.068\r\n10.1007/s11664-009-0735-1,0.0015,-83,0.14,Mg2Si0.6Ge0.4Bi0.02,\"solid state reaction, He/H2\",polycrystalline,300,2.98,32.68,2694000,5169,1229,258.35,21.529,12,667,0.000459,6890,0.164\r\n10.1007/s11664-009-0735-1,1.24,26,1.64E-05,Mg2Si0.98Ag0.02,\"solid state reaction, He/H2\",polycrystalline,300,7.83,26.1,353300,4954,699.7,258.55,21.546,12,0.806,5.45E-08,676,7.54E-05\r\n10.1007/s11664-009-0735-1,0.051,30,0.000541,Mg2Si0.6Ge0.4Ag0.02,\"solid state reaction, He/H2\",polycrystalline,300,4.11,32.01,493400,5075,1026,258.35,21.529,12,19.5,1.80E-06,925,0.00347\r\n10.1007/s11664-009-0735-1,0.00121,-110,0.4,Mg2Si0.98Bi0.02,\"solid state reaction, He/H2\",polycrystalline,400,5.63,26.77,3061000,5072,957.2,258.55,21.546,12,826,0.00101,12200,0.143\r\n10.1007/s11664-009-0735-1,0.00127,-118,0.43,Mg2Si0.6Ge0.4Bi0.02,\"solid state reaction, He/H2\",polycrystalline,400,2.62,32.68,2694000,5169,1229,258.35,21.529,12,787,0.00109,13800,0.293\r\n10.1007/s11664-009-0735-1,0.413,178,0.00307,Mg2Si0.98Ag0.02,\"solid state reaction, He/H2\",polycrystalline,400,6.06,26.1,353300,4954,699.7,258.55,21.546,12,2.421,7.67E-06,31700,0.00039\r\n10.1007/s11664-009-0735-1,0.028,158,0.04,Mg2Si0.6Ge0.4Ag0.02,\"solid state reaction, He/H2\",polycrystalline,400,3.09,32.01,493400,5075,1026,258.35,21.529,12,35.2,8.78E-05,24900,0.011\r\n10.1007/s11664-009-0735-1,0.00125,-175,1.72,Mg2Si0.98Bi0.02,\"solid state reaction, He/H2\",polycrystalline,700,3.6,26.77,3061000,5072,957.2,258.55,21.546,12,802,0.00245,30600,0.38\r\n10.1007/s11664-009-0735-1,0.00137,-176,1.59,Mg2Si0.6Ge0.4Bi0.02,\"solid state reaction, He/H2\",polycrystalline,700,1.94,32.68,2694000,5169,1229,258.35,21.529,12,730,0.00227,31000,0.643\r\n10.1007/s11664-009-0735-1,0.04,149,0.04,Mg2Si0.98Ag0.02,\"solid state reaction, He/H2\",polycrystalline,700,3.67,26.1,353300,4954,699.7,258.55,21.546,12,25.2,5.59E-05,22200,0.012\r\n10.1007/s11664-009-0735-1,0.015,319,0.48,Mg2Si0.6Ge0.4Ag0.02,\"solid state reaction, He/H2\",polycrystalline,700,2.57,32.01,493400,5075,1026,258.35,21.529,12,67.1,0.000682,102000,0.045\r\n10.1007/s11664-009-0735-1,0.00186,-212,2.43,Mg2Si0.98Bi0.02,\"solid state reaction, He/H2\",polycrystalline,1000,2.75,26.77,3061000,5072,957.2,258.55,21.546,12,539,0.00243,45100,0.478\r\n10.1007/s11664-009-0735-1,0.0022,-188,1.6,Mg2Si0.6Ge0.4Bi0.02,\"solid state reaction, He/H2\",polycrystalline,1000,1.73,32.68,2694000,5169,1229,258.35,21.529,12,455,0.0016,35200,0.641\r\n10.1007/s11664-009-0735-1,0.0066,192,0.56,Mg2Si0.98Ag0.02,\"solid state reaction, He/H2\",polycrystalline,1000,3.16,26.1,353300,4954,699.7,258.55,21.546,12,152,0.000559,36900,0.117\r\n10.1007/s11664-009-0735-1,0.00544,224,0.92,Mg2Si0.6Ge0.4Ag0.02,\"solid state reaction, He/H2\",polycrystalline,1000,3.48,32.01,493400,5075,1026,258.35,21.529,12,184,0.000922,50200,0.129\r\n10.1007/s11664-009-0815-2,0.107,277,0.02,Cu1Fe0.9Cr0.1O2,Solid state reaction,polycrystalline,300,,37.75,6756,1683,1344,136.95,11.412,12,9.339,7.17E-05,76800,\r\n10.1007/s11664-009-0815-2,0.0018,98,0.16,Cu1Rh0.9Mg0.1O2,Solid state reaction,polycrystalline,300,,47.65,485900000,2250,4486,140.56,11.713,12,557,0.000531,9540,\r\n10.1007/s11664-009-0815-2,0.197,300,0.01,Cu1Cr0.98Mg0.02O2,Solid state reaction,polycrystalline,300,,36.75,8512,1883,2174,131.12,10.927,12,5.085,4.58E-05,90000,\r\n10.1007/s11664-009-0815-2,0.051,-132,0.01,Zn0.9975Al0.0025O1,\"solid state reaction, vacuum\",polycrystalline,300,,40.64,10770,1363,1620,47.62,11.905,4,19.6,3.41E-05,17400,\r\n10.1007/s11664-009-0815-2,0.015,-115,0.03,Zn0.995Al0.005O1,\"solid state reaction, vacuum\",polycrystalline,300,,40.59,10760,1362,1619,47.62,11.905,4,66.2,8.82E-05,13300,\r\n10.1007/s11664-009-0815-2,0.01,-114,0.04,Zn0.9925Al0.0075O1,\"solid state reaction, vacuum\",polycrystalline,300,,40.55,10740,1362,1618,47.62,11.905,4,97,0.000126,13000,\r\n10.1007/s11664-009-0815-2,0.00678,-111,0.05,Zn0.99Al0.01O1,\"solid state reaction, vacuum\",polycrystalline,300,,40.5,10730,1362,1616,47.62,11.905,4,148,0.000182,12300,\r\n10.1007/s11664-009-0815-2,0.021,-145,0.03,Zn0.97Al0.03O1,\"solid state reaction, vacuum\",polycrystalline,300,,40.11,10610,1360,1608,47.62,11.905,4,46.7,9.81E-05,21000,\r\n10.1007/s11664-009-0815-2,0.07,299,0.05,Cu1Fe0.9Cr0.1O2,Solid state reaction,polycrystalline,400,,37.75,6756,1683,1344,136.95,11.412,12,14.3,0.000128,89400,\r\n10.1007/s11664-009-0815-2,0.00194,115,0.27,Cu1Rh0.9Mg0.1O2,Solid state reaction,polycrystalline,400,,47.65,485900000,2250,4486,140.56,11.713,12,516,0.000684,13300,\r\n10.1007/s11664-009-0815-2,0.119,321,0.03,Cu1Cr0.98Mg0.02O2,Solid state reaction,polycrystalline,400,,36.75,8512,1883,2174,131.12,10.927,12,8.396,8.67E-05,103000,\r\n10.1007/s11664-009-0815-2,0.05,-135,0.01,Zn0.9975Al0.0025O1,\"solid state reaction, vacuum\",polycrystalline,400,,40.64,10770,1363,1620,47.62,11.905,4,19.8,3.61E-05,18200,\r\n10.1007/s11664-009-0815-2,0.015,-128,0.04,Zn0.995Al0.005O1,\"solid state reaction, vacuum\",polycrystalline,400,,40.59,10760,1362,1619,47.62,11.905,4,66.5,0.00011,16500,\r\n10.1007/s11664-009-0815-2,0.01,-123,0.06,Zn0.9925Al0.0075O1,\"solid state reaction, vacuum\",polycrystalline,400,,40.55,10740,1362,1618,47.62,11.905,4,97,0.000148,15300,\r\n10.1007/s11664-009-0815-2,0.00709,-117,0.08,Zn0.99Al0.01O1,\"solid state reaction, vacuum\",polycrystalline,400,,40.5,10730,1362,1616,47.62,11.905,4,141,0.000194,13700,\r\n10.1007/s11664-009-0815-2,0.021,-150,0.04,Zn0.97Al0.03O1,\"solid state reaction, vacuum\",polycrystalline,400,,40.11,10610,1360,1608,47.62,11.905,4,46.6,0.000105,22500,\r\n10.1007/s11664-009-0815-2,0.056,321,0.13,Cu1Fe0.9Cr0.1O2,Solid state reaction,polycrystalline,700,,37.75,6756,1683,1344,136.95,11.412,12,18,0.000185,103000,\r\n10.1007/s11664-009-0815-2,0.0032,146,0.46,Cu1Rh0.9Mg0.1O2,Solid state reaction,polycrystalline,700,,47.65,485900000,2250,4486,140.56,11.713,12,313,0.000662,21200,\r\n10.1007/s11664-009-0815-2,0.087,352,0.1,Cu1Cr0.98Mg0.02O2,Solid state reaction,polycrystalline,700,,36.75,8512,1883,2174,131.12,10.927,12,11.6,0.000143,124000,\r\n10.1007/s11664-009-0815-2,0.041,-181,0.06,Zn0.9975Al0.0025O1,\"solid state reaction, vacuum\",polycrystalline,700,,40.64,10770,1363,1620,47.62,11.905,4,24.2,7.92E-05,32700,\r\n10.1007/s11664-009-0815-2,0.015,-163,0.12,Zn0.995Al0.005O1,\"solid state reaction, vacuum\",polycrystalline,700,,40.59,10760,1362,1619,47.62,11.905,4,64.8,0.000172,26500,\r\n10.1007/s11664-009-0815-2,0.011,-155,0.15,Zn0.9925Al0.0075O1,\"solid state reaction, vacuum\",polycrystalline,700,,40.55,10740,1362,1618,47.62,11.905,4,90.1,0.000215,23900,\r\n10.1007/s11664-009-0815-2,0.00796,-147,0.19,Zn0.99Al0.01O1,\"solid state reaction, vacuum\",polycrystalline,700,,40.5,10730,1362,1616,47.62,11.905,4,126,0.000272,21600,\r\n10.1007/s11664-009-0815-2,0.022,-178,0.1,Zn0.97Al0.03O1,\"solid state reaction, vacuum\",polycrystalline,700,,40.11,10610,1360,1608,47.62,11.905,4,45.2,0.000143,31500,\r\n10.1007/s11664-009-0815-2,0.053,325,0.2,Cu1Fe0.9Cr0.1O2,Solid state reaction,polycrystalline,1000,,37.75,6756,1683,1344,136.95,11.412,12,18.8,0.000198,106000,\r\n10.1007/s11664-009-0815-2,0.00408,168,0.69,Cu1Rh0.9Mg0.1O2,Solid state reaction,polycrystalline,1000,,47.65,485900000,2250,4486,140.56,11.713,12,245,0.000691,28200,\r\n10.1007/s11664-009-0815-2,0.072,355,0.17,Cu1Cr0.98Mg0.02O2,Solid state reaction,polycrystalline,1000,,36.75,8512,1883,2174,131.12,10.927,12,13.9,0.000175,126000,\r\n10.1007/s11664-009-0815-2,0.024,-219,0.2,Zn0.9975Al0.0025O1,\"solid state reaction, vacuum\",polycrystalline,1000,,40.64,10770,1363,1620,47.62,11.905,4,41.8,0.0002,47800,\r\n10.1007/s11664-009-0815-2,0.011,-205,0.38,Zn0.995Al0.005O1,\"solid state reaction, vacuum\",polycrystalline,1000,,40.59,10760,1362,1619,47.62,11.905,4,91.4,0.000383,41900,\r\n10.1007/s11664-009-0815-2,0.00953,-188,0.37,Zn0.9925Al0.0075O1,\"solid state reaction, vacuum\",polycrystalline,1000,,40.55,10740,1362,1618,47.62,11.905,4,105,0.00037,35300,\r\n10.1007/s11664-009-0815-2,0.00772,-176,0.4,Zn0.99Al0.01O1,\"solid state reaction, vacuum\",polycrystalline,1000,,40.5,10730,1362,1616,47.62,11.905,4,130,0.0004,30900,\r\n10.1007/s11664-009-0815-2,0.017,-208,0.25,Zn0.97Al0.03O1,\"solid state reaction, vacuum\",polycrystalline,1000,,40.11,10610,1360,1608,47.62,11.905,4,58.6,0.000252,43100,\r\n10.1007/s11664-009-0975-0,0.000509,22,0.03,Cr1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,300,1.938,58.82,557400,1985,3955,269.41,17.608,15.3,1970,9.09E-05,463,0.742\r\n10.1007/s11664-009-0975-0,0.00069,27,0.03,Mn1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,300,1.432,59.07,554800,1871,3777,816.76,18.15,45,1450,0.000108,745,0.74\r\n10.1007/s11664-009-0975-0,0.00065,23,0.02,Fe1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,300,1.488,59.14,554000,1937,3740,807.22,17.938,45,1540,7.88E-05,512,0.757\r\n10.1007/s11664-009-0975-0,0.000618,8,0.00332,Ni2.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,300,1.714,59.35,528800,1782,3642,801.34,16.695,48,1620,1.11E-05,68.3,0.691\r\n10.1007/s11664-009-0975-0,0.000832,48,0.08,Cu4.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,300,1.348,60.36,465000,1820,3380,853.58,15.807,54,1200,0.000275,2280,0.653\r\n10.1007/s11664-009-0975-0,0.000552,27,0.05,Cr1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,400,2.106,58.82,557400,1985,3955,269.41,17.608,15.3,1810,0.000133,733,0.84\r\n10.1007/s11664-009-0975-0,0.000737,31,0.05,Mn1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,400,1.627,59.07,554800,1871,3777,816.76,18.15,45,1360,0.00013,960,0.814\r\n10.1007/s11664-009-0975-0,0.000673,28,0.05,Fe1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,400,1.852,59.14,554000,1937,3740,807.22,17.938,45,1490,0.000118,795,0.783\r\n10.1007/s11664-009-0975-0,0.000512,9,0.00657,Ni2.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,400,2.33,59.35,528800,1782,3642,801.34,16.695,48,1950,1.64E-05,84.1,0.819\r\n10.1007/s11664-009-0975-0,0.00102,62,0.15,Cu4.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,400,1.431,60.36,465000,1820,3380,853.58,15.807,54,976,0.00037,3790,0.666\r\n10.1007/s11664-009-0975-0,0.000693,51,0.26,Cr1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,700,2.69,58.82,557400,1985,3955,269.41,17.608,15.3,1440,0.000378,2620,0.916\r\n10.1007/s11664-009-0975-0,0.000878,48,0.18,Mn1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,700,2.353,59.07,554800,1871,3777,816.76,18.15,45,1140,0.000259,2270,0.827\r\n10.1007/s11664-009-0975-0,0.00076,45,0.19,Fe1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,700,2.775,59.14,554000,1937,3740,807.22,17.938,45,1320,0.00027,2050,0.81\r\n10.1007/s11664-009-0975-0,0.000457,21,0.07,Ni2.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,700,4.237,59.35,528800,1782,3642,801.34,16.695,48,2190,9.49E-05,434,0.883\r\n10.1007/s11664-009-0975-0,0.00169,105,0.46,Cu4.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,700,1.791,60.36,465000,1820,3380,853.58,15.807,54,592,0.000657,11100,0.565\r\n10.1007/s11664-009-0975-0,0.000814,70,0.6,Cr1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,1000,3.192,58.82,557400,1985,3955,269.41,17.608,15.3,1230,0.000601,4890,0.939\r\n10.1007/s11664-009-0975-0,0.000962,57,0.34,Mn1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,1000,2.882,59.07,554800,1871,3777,816.76,18.15,45,1040,0.000343,3300,0.88\r\n10.1007/s11664-009-0975-0,0.000826,54,0.35,Fe1.3Mo6S8,\"solid state reaction, vacuum\",polycrystalline,1000,3.416,59.14,554000,1937,3740,807.22,17.938,45,1210,0.000352,2910,0.865\r\n10.1007/s11664-009-0975-0,0.000468,33,0.24,Ni2.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,1000,5.975,59.35,528800,1782,3642,801.34,16.695,48,2140,0.000236,1100,0.872\r\n10.1007/s11664-009-0975-0,0.00218,133,0.81,Cu4.0Mo6S8,\"solid state reaction, vacuum\",polycrystalline,1000,2.039,60.36,465000,1820,3380,853.58,15.807,54,459,0.000812,17700,0.549\r\n10.1016/0022-4596(91)90248-G,0.00576,-75,0.03,Ca0.9Tb0.1Mn1O3,Solid state reaction,polycrystalline,300,1.484,30.98,96250,2591,1460,209.58,10.479,20,174,9.76E-05,5620,0.086\r\n10.1016/0022-4596(91)90248-G,0.00607,-46,0.01,Ca0.7Tb0.3Mn1O3,Solid state reaction,polycrystalline,300,2.17,35.73,249700,3759,1755,213.15,10.658,20,165,3.53E-05,2140,0.056\r\n10.1016/0022-4596(91)90248-G,0.00669,-72,0.02,Ca0.9Ho0.1Mn1O3,Solid state reaction,polycrystalline,300,1.637,31.1,85220,2618,1467,209.04,10.452,20,149,7.75E-05,5190,0.067\r\n10.1016/0022-4596(91)90248-G,0.00512,-44,0.01,Ca0.7Ho0.3Mn1O3,Solid state reaction,polycrystalline,300,2.144,36.09,219600,3816,1769,212.3,10.615,20,195,3.73E-05,1910,0.067\r\n10.1016/0022-4596(91)90248-G,0.00437,-71,0.03,Ca0.9Y0.1Mn1O3,Solid state reaction,polycrystalline,300,1.489,29.58,2323,2287,1352,212.3,10.615,20,229,0.000114,4970,0.112\r\n10.1016/0022-4596(91)90248-G,0.00763,-42,0.00681,Ca0.7Y0.3Mn1O3,Solid state reaction,polycrystalline,300,1.793,31.53,5816,3058,1490,219.83,10.992,20,131,2.27E-05,1730,0.054\r\n10.1016/0022-4596(91)90248-G,0.00639,-94,0.06,Ca0.9Tb0.1Mn1O3,Solid state reaction,polycrystalline,400,1.571,30.98,96250,2591,1460,209.58,10.479,20,157,0.000138,8800,0.097\r\n10.1016/0022-4596(91)90248-G,0.0055,-44,0.01,Ca0.7Tb0.3Mn1O3,Solid state reaction,polycrystalline,400,1.466,35.73,249700,3759,1755,213.15,10.658,20,182,3.58E-05,1970,0.121\r\n10.1016/0022-4596(91)90248-G,0.0074,-82,0.04,Ca0.9Ho0.1Mn1O3,Solid state reaction,polycrystalline,400,1.546,31.1,85220,2618,1467,209.04,10.452,20,135,9.04E-05,6690,0.085\r\n10.1016/0022-4596(91)90248-G,0.0044,-45,0.02,Ca0.7Ho0.3Mn1O3,Solid state reaction,polycrystalline,400,1.524,36.09,219600,3816,1769,212.3,10.615,20,228,4.62E-05,2030,0.146\r\n10.1016/0022-4596(91)90248-G,0.00478,-82,0.06,Ca0.9Y0.1Mn1O3,Solid state reaction,polycrystalline,400,1.482,29.58,2323,2287,1352,212.3,10.615,20,209,0.00014,6680,0.138\r\n10.1016/0022-4596(91)90248-G,0.00649,-42,0.01,Ca0.7Y0.3Mn1O3,Solid state reaction,polycrystalline,400,1.467,31.53,5816,3058,1490,219.83,10.992,20,154,2.67E-05,1730,0.102\r\n10.1016/0022-4596(91)90248-G,0.00832,-125,0.13,Ca0.9Tb0.1Mn1O3,Solid state reaction,polycrystalline,700,1.575,30.98,96250,2591,1460,209.58,10.479,20,120,0.000187,15500,0.13\r\n10.1016/0022-4596(91)90248-G,0.00526,-55,0.04,Ca0.7Tb0.3Mn1O3,Solid state reaction,polycrystalline,700,1.462,35.73,249700,3759,1755,213.15,10.658,20,190,5.82E-05,3060,0.222\r\n10.1016/0022-4596(91)90248-G,0.0095,-101,0.08,Ca0.9Ho0.1Mn1O3,Solid state reaction,polycrystalline,700,1.518,31.1,85220,2618,1467,209.04,10.452,20,105,0.000108,10300,0.118\r\n10.1016/0022-4596(91)90248-G,0.00377,-51,0.05,Ca0.7Ho0.3Mn1O3,Solid state reaction,polycrystalline,700,1.417,36.09,219600,3816,1769,212.3,10.615,20,265,6.90E-05,2600,0.32\r\n10.1016/0022-4596(91)90248-G,0.00592,-113,0.15,Ca0.9Y0.1Mn1O3,Solid state reaction,polycrystalline,700,1.601,29.58,2323,2287,1352,212.3,10.615,20,169,0.000215,12700,0.18\r\n10.1016/0022-4596(91)90248-G,0.00628,-52,0.03,Ca0.7Y0.3Mn1O3,Solid state reaction,polycrystalline,700,1.515,31.53,5816,3058,1490,219.83,10.992,20,159,4.38E-05,2750,0.18\r\n10.1016/0022-4596(91)90248-G,0.01,-152,0.23,Ca0.9Tb0.1Mn1O3,Solid state reaction,polycrystalline,1000,1.604,30.98,96250,2591,1460,209.58,10.479,20,97.6,0.000227,23200,0.148\r\n10.1016/0022-4596(91)90248-G,0.00559,-68,0.08,Ca0.7Tb0.3Mn1O3,Solid state reaction,polycrystalline,1000,1.681,35.73,249700,3759,1755,213.15,10.658,20,179,8.33E-05,4650,0.26\r\n10.1016/0022-4596(91)90248-G,0.012,-115,0.11,Ca0.9Ho0.1Mn1O3,Solid state reaction,polycrystalline,1000,1.471,31.1,85220,2618,1467,209.04,10.452,20,86.4,0.000113,13100,0.143\r\n10.1016/0022-4596(91)90248-G,0.00423,-65,0.1,Ca0.7Ho0.3Mn1O3,Solid state reaction,polycrystalline,1000,1.599,36.09,219600,3816,1769,212.3,10.615,20,237,9.91E-05,4190,0.361\r\n10.1016/0022-4596(91)90248-G,0.0071,-136,0.26,Ca0.9Y0.1Mn1O3,Solid state reaction,polycrystalline,1000,1.629,29.58,2323,2287,1352,212.3,10.615,20,141,0.000259,18400,0.211\r\n10.1016/0022-4596(91)90248-G,0.00707,-61,0.05,Ca0.7Y0.3Mn1O3,Solid state reaction,polycrystalline,1000,1.537,31.53,5816,3058,1490,219.83,10.992,20,141,5.23E-05,3700,0.225\r\n10.1016/j.jallcom.2003.07.016,0.000494,-82,0.41,Ba0.3Sr0.6La0.1Ti1O3,\"solid state reaction , Ar\",polycrystalline,300,4.07,40.7,3096,2709,1946,59.36,11.872,5,2030,0.00137,6760,0.364\r\n10.1016/j.jallcom.2003.07.016,0.000763,-101,0.54,Ba0.3Sr0.6La0.1Ti1O3,\"solid state reaction , Ar\",polycrystalline,400,3.36,40.7,3096,2709,1946,59.36,11.872,5,1310,0.00135,10300,0.381\r\n10.1016/j.jallcom.2003.07.016,0.00273,-163,0.68,Ba0.3Sr0.6La0.1Ti1O3,\"solid state reaction , Ar\",polycrystalline,700,1.91,40.7,3096,2709,1946,59.36,11.872,5,366,0.000973,26600,0.328\r\n10.1016/j.jallcom.2004.02.061,0.00105,-133,0.51,Zr1Ni1.98Cu0.02Sn1,\"arc melted, Ar\",polycrystalline,300,7.98,81.85,165700,2246,1848,228.44,19.037,12,952,0.00168,17700,0.087\r\n10.1016/j.jallcom.2004.02.061,0.00876,-95,0.03,Zr1Ni0.76Co0.004Cu0.2Sn1,\"arc melted, Ar\",polycrystalline,300,6.02,90.24,201300,2555,1934,228.44,19.037,12,114,0.000103,9020,0.014\r\n10.1016/j.jallcom.2004.02.061,0.00117,-136,0.63,Zr1Ni1.98Cu0.02Sn1,\"arc melted, Ar\",polycrystalline,400,6.795,81.85,165700,2246,1848,228.44,19.037,12,855,0.00158,18500,0.123\r\n10.1016/j.jallcom.2004.02.061,0.00695,-130,0.1,Zr1Ni0.76Co0.004Cu0.2Sn1,\"arc melted, Ar\",polycrystalline,400,5.3,90.24,201300,2555,1934,228.44,19.037,12,144,0.000243,16900,0.026\r\n10.1016/j.jallcom.2004.05.078,0.00932,-177,0.1,Zr0.5Hf0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,3.949,104.09,262000,2643,2022,226.87,18.906,12,107,0.000337,31400,0.02\r\n10.1016/j.jallcom.2004.05.078,0.00241,-250,0.78,Zr0.5Hf0.5Ni1Sn1.998Sb0.002,\"arc-melted, Ar\",polycrystalline,300,2.887,107.74,314900,2632,1917,226.87,18.906,12,415,0.0026,62500,0.105\r\n10.1016/j.jallcom.2004.05.078,0.00117,-211,1.15,Zr0.5Hf0.5Ni1Sn1.994Sb0.006,\"arc-melted, Ar\",polycrystalline,300,2.767,107.75,320000,2638,1919,226.87,18.906,12,858,0.00382,44500,0.227\r\n10.1016/j.jallcom.2004.05.078,0.00877,-182,0.11,Zr0.4Hf0.4Ti0.2Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,,98.29,258100,2524,1954,226.87,18.906,12,114,0.000377,33000,\r\n10.1016/j.jallcom.2004.05.078,0.00841,-330,0.39,Zr0.35Hf0.35Ti0.3Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,,95.39,256000,2459,1917,226.87,18.906,12,119,0.00129,109000,\r\n10.1016/j.jallcom.2004.05.078,0.00846,-316,0.35,Zr0.3Hf0.3Ti0.4Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,,92.49,253700,2389,1878,226.87,18.906,12,118,0.00118,100000,\r\n10.1016/j.jallcom.2004.05.078,0.00495,-304,0.56,Zr0.25Hf0.25Ti0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,,89.59,251300,2315,1836,226.87,18.906,12,202,0.00186,92200,\r\n10.1016/j.jallcom.2004.05.078,0.00467,-251,0.4,Zr0.15Hf0.15Ti0.7Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,,83.79,246000,2152,1744,226.87,18.906,12,214,0.00135,62900,\r\n10.1016/j.jallcom.2004.05.078,0.00217,-281,1.46,Zr0.5Hf0.5Ni1Sn1.998Sb0.002,\"arc-melted, Ar\",polycrystalline,400,2.713,107.74,314900,2632,1917,226.87,18.906,12,461,0.00364,79000,0.166\r\n10.1016/j.jallcom.2004.05.078,0.00125,-237,1.79,Zr0.5Hf0.5Ni1Sn1.994Sb0.006,\"arc-melted, Ar\",polycrystalline,400,2.646,107.75,320000,2638,1919,226.87,18.906,12,798,0.00448,56200,0.295\r\n10.1016/j.jallcom.2004.05.078,0.00236,-238,1.68,Zr0.5Hf0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,3.113,104.09,262000,2643,2022,226.87,18.906,12,423,0.0024,56600,0.232\r\n10.1016/j.jallcom.2004.05.078,0.00154,-307,4.27,Zr0.5Hf0.5Ni1Sn1.998Sb0.002,\"arc-melted, Ar\",polycrystalline,700,2.947,107.74,314900,2632,1917,226.87,18.906,12,648,0.0061,94200,0.375\r\n10.1016/j.jallcom.2004.05.078,0.00132,-274,3.99,Zr0.5Hf0.5Ni1Sn1.994Sb0.006,\"arc-melted, Ar\",polycrystalline,700,2.964,107.75,320000,2638,1919,226.87,18.906,12,758,0.00569,75100,0.437\r\n10.1016/j.jallcom.2004.05.078,0.00215,-287,2.69,Zr0.4Hf0.4Ti0.2Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,,98.29,258100,2524,1954,226.87,18.906,12,465,0.00384,82500,\r\n10.1016/j.jallcom.2004.05.078,0.00235,-345,3.55,Zr0.35Hf0.35Ti0.3Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,,95.39,256000,2459,1917,226.87,18.906,12,426,0.00508,119000,\r\n10.1016/j.jallcom.2004.05.078,0.00203,-358,4.41,Zr0.3Hf0.3Ti0.4Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,,92.49,253700,2389,1878,226.87,18.906,12,492,0.00631,128000,\r\n10.1016/j.jallcom.2004.05.078,0.00189,-334,4.13,Zr0.25Hf0.25Ti0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,,89.59,251300,2315,1836,226.87,18.906,12,530,0.0059,111000,\r\n10.1016/j.jallcom.2004.05.078,0.00168,-261,2.83,Zr0.15Hf0.15Ti0.7Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,,83.79,246000,2152,1744,226.87,18.906,12,594,0.00404,68100,\r\n10.1016/j.jallcom.2005.04.060,0.048,-191,0.02,Fe0.998Co0.002Si2,\"arc-melted, Ar\",polycrystalline,300,5.69,37.34,48.87,3570,1187,601.91,12.54,48,21.1,7.68E-05,36500,0.00271\r\n10.1016/j.jallcom.2005.04.060,0.128,-318,0.02,Fe0.978Co0.00196Si1.96Y0.04O0.06,\"arc-melted, Ar\",polycrystalline,300,4.59,37.6,1051,3739,1227,601.91,12.54,48,7.843,7.93E-05,101000,0.00125\r\n10.1016/j.jallcom.2005.04.060,0.27,-226,0.00568,Fe0.978Co0.00196Si1.96Y0.12O0.18,\"arc-melted, Ar\",polycrystalline,300,2.86,38.06,2834,4040,1297,601.91,12.54,48,3.704,1.89E-05,51100,0.000948\r\n10.1016/j.jallcom.2005.04.060,0.026,-183,0.05,Fe0.998Co0.002Si2,\"arc-melted, Ar\",polycrystalline,400,5.34,37.34,48.87,3570,1187,601.91,12.54,48,38.5,0.000129,33500,0.00703\r\n10.1016/j.jallcom.2005.04.060,0.056,-327,0.08,Fe0.978Co0.00196Si1.96Y0.04O0.06,\"arc-melted, Ar\",polycrystalline,400,4.09,37.6,1051,3739,1227,601.91,12.54,48,17.8,0.00019,107000,0.00424\r\n10.1016/j.jallcom.2005.04.060,0.15,-227,0.01,Fe0.978Co0.00196Si1.96Y0.12O0.18,\"arc-melted, Ar\",polycrystalline,400,2.64,38.06,2834,4040,1297,601.91,12.54,48,6.689,3.45E-05,51500,0.00247\r\n10.1016/j.jallcom.2005.04.060,0.012,-181,0.19,Fe0.998Co0.002Si2,\"arc-melted, Ar\",polycrystalline,700,4.9,37.34,48.87,3570,1187,601.91,12.54,48,81.3,0.000265,32600,0.028\r\n10.1016/j.jallcom.2005.04.060,0.024,-287,0.24,Fe0.978Co0.00196Si1.96Y0.04O0.06,\"arc-melted, Ar\",polycrystalline,700,3.95,37.6,1051,3739,1227,601.91,12.54,48,41.7,0.000343,82400,0.018\r\n10.1016/j.jallcom.2005.04.060,0.052,-222,0.07,Fe0.978Co0.00196Si1.96Y0.12O0.18,\"arc-melted, Ar\",polycrystalline,700,2.96,38.06,2834,4040,1297,601.91,12.54,48,19.3,9.51E-05,49300,0.011\r\n10.1016/j.jallcom.2005.04.060,0.00605,-87,0.13,Fe0.998Co0.002Si2,\"arc-melted, Ar\",polycrystalline,1000,5.02,37.34,48.87,3570,1187,601.91,12.54,48,165,0.000126,7620,0.08\r\n10.1016/j.jallcom.2005.04.060,0.012,-101,0.08,Fe0.978Co0.00196Si1.96Y0.04O0.06,\"arc-melted, Ar\",polycrystalline,1000,4.21,37.6,1051,3739,1227,601.91,12.54,48,82,8.33E-05,10200,0.048\r\n10.1016/j.jallcom.2005.04.060,0.021,-68,0.02,Fe0.978Co0.00196Si1.96Y0.12O0.18,\"arc-melted, Ar\",polycrystalline,1000,3.22,38.06,2834,4040,1297,601.91,12.54,48,46.7,2.16E-05,4620,0.035\r\n10.1016/j.jallcom.2006.02.075,0.000598,-113,0.64,Zr1Ni1Sn0.98Sb0.02,\"arc melted, Ar\",polycrystalline,300,8.5,89.56,241400,2567,1945,228.44,19.037,12,1670,0.00214,12800,0.144\r\n10.1016/j.jallcom.2006.02.075,0.000771,-92,0.33,Zr0.94Y0.06Ni1Sn0.96Sb0.04,\"arc melted, Ar\",polycrystalline,300,8.35,89.54,283400,2742,1962,228.44,19.037,12,1300,0.0011,8460,0.114\r\n10.1016/j.jallcom.2006.02.075,0.000624,-137,1.2,Zr1Ni1Sn0.98Sb0.02,\"arc melted, Ar\",polycrystalline,400,7.95,89.56,241400,2567,1945,228.44,19.037,12,1600,0.00301,18800,0.197\r\n10.1016/j.jallcom.2006.02.075,0.000788,-109,0.6,Zr0.94Y0.06Ni1Sn0.96Sb0.04,\"arc melted, Ar\",polycrystalline,400,6.51,89.54,283400,2742,1962,228.44,19.037,12,1270,0.00151,11900,0.19\r\n10.1016/j.jallcom.2007.09.101,0.00162,-89,0.15,Mg2Si1,\"melted, Ar\",polycrystalline,300,4.5,25.57,27.34,5057,683.1,258.55,21.546,12,616,0.000488,7920,0.1\r\n10.1016/j.jallcom.2007.09.101,0.00104,-75,0.16,Mg1.95Ca0.05Si1,\"melted, Ar\",polycrystalline,300,5.6,25.83,27.02,5023,707.1,258.55,21.546,12,964,0.00054,5600,0.126\r\n10.1016/j.jallcom.2007.09.101,0.00212,-61,0.05,Mg1.9Ca0.1Si1,\"melted, Ar\",polycrystalline,300,5.2,26.09,26.71,4990,730.6,258.55,21.546,12,472,0.000176,3720,0.066\r\n10.1016/j.jallcom.2007.09.101,0.00198,-189,0.72,Mg2Si1,\"melted, Ar\",polycrystalline,400,4,25.57,27.34,5057,683.1,258.55,21.546,12,506,0.00181,35700,0.123\r\n10.1016/j.jallcom.2007.09.101,0.00115,-95,0.31,Mg1.95Ca0.05Si1,\"melted, Ar\",polycrystalline,400,4.9,25.83,27.02,5023,707.1,258.55,21.546,12,870,0.000781,8990,0.173\r\n10.1016/j.jallcom.2007.09.101,0.00214,-74,0.1,Mg1.9Ca0.1Si1,\"melted, Ar\",polycrystalline,400,4.7,26.09,26.71,4990,730.6,258.55,21.546,12,467,0.000256,5480,0.097\r\n10.1016/j.jallcom.2007.09.101,0.0038,-267,1.31,Mg2Si1,\"melted, Ar\",polycrystalline,700,3.25,25.57,27.34,5057,683.1,258.55,21.546,12,263,0.00188,71300,0.138\r\n10.1016/j.jallcom.2007.09.101,0.00255,-153,0.64,Mg1.95Ca0.05Si1,\"melted, Ar\",polycrystalline,700,3.8,25.83,27.02,5023,707.1,258.55,21.546,12,392,0.000917,23400,0.176\r\n10.1016/j.jallcom.2007.09.101,0.00275,-130,0.43,Mg1.9Ca0.1Si1,\"melted, Ar\",polycrystalline,700,3.8,26.09,26.71,4990,730.6,258.55,21.546,12,364,0.000614,16900,0.163\r\n10.1016/j.jallcom.2008.02.041,0.031,-271,0.07,Ti1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,6.076,75.09,236400,1861,1579,208.21,17.351,12,31.8,0.000234,73600,0.00383\r\n10.1016/j.jallcom.2008.02.041,0.00116,-177,0.82,Ti0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,6.893,75.24,236100,1890,1609,208.21,17.351,12,866,0.00272,31400,0.092\r\n10.1016/j.jallcom.2008.02.041,0.000654,-140,0.9,Ti0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,7.426,75.39,235900,1918,1638,208.21,17.351,12,1530,0.003,19600,0.151\r\n10.1016/j.jallcom.2008.02.041,0.000351,-96,0.79,Ti0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,6.96,75.84,235200,2004,1726,208.21,17.351,12,2850,0.00264,9260,0.3\r\n10.1016/j.jallcom.2008.02.041,0.031,-354,0.12,Zr1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,10.143,89.54,200100,2519,1929,226.87,18.906,12,31.8,0.000398,125000,0.0023\r\n10.1016/j.jallcom.2008.02.041,0.0011,-171,0.8,Zr0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,9.676,89.55,200200,2537,1950,226.87,18.906,12,913,0.00267,29200,0.069\r\n10.1016/j.jallcom.2008.02.041,0.000616,-131,0.84,Zr0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,10.059,89.55,200400,2554,1972,226.87,18.906,12,1620,0.0028,17300,0.118\r\n10.1016/j.jallcom.2008.02.041,0.000337,-78,0.54,Zr0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,300,8.859,89.57,200900,2608,2036,226.87,18.906,12,2970,0.00181,6110,0.245\r\n10.1016/j.jallcom.2008.02.041,0.00839,-296,0.42,Ti1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,5.195,75.09,236400,1861,1579,208.21,17.351,12,119,0.00104,87600,0.022\r\n10.1016/j.jallcom.2008.02.041,0.00124,-192,1.19,Ti0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,5.862,75.24,236100,1890,1609,208.21,17.351,12,806,0.00299,37000,0.134\r\n10.1016/j.jallcom.2008.02.041,0.000727,-159,1.38,Ti0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,6.328,75.39,235900,1918,1638,208.21,17.351,12,1380,0.00346,25100,0.212\r\n10.1016/j.jallcom.2008.02.041,0.000396,-111,1.24,Ti0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,6.378,75.84,235200,2004,1726,208.21,17.351,12,2530,0.00311,12300,0.387\r\n10.1016/j.jallcom.2008.02.041,0.00874,-343,0.54,Zr1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,8.395,89.54,200100,2519,1929,226.87,18.906,12,114,0.00134,117000,0.013\r\n10.1016/j.jallcom.2008.02.041,0.00124,-189,1.15,Zr0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,8.212,89.55,200200,2537,1950,226.87,18.906,12,806,0.00288,35700,0.096\r\n10.1016/j.jallcom.2008.02.041,0.000691,-148,1.27,Zr0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,8.678,89.55,200400,2554,1972,226.87,18.906,12,1450,0.00318,22000,0.163\r\n10.1016/j.jallcom.2008.02.041,0.000364,-89,0.87,Zr0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,400,8.212,89.57,200900,2608,2036,226.87,18.906,12,2740,0.00218,7930,0.326\r\n10.1016/j.jallcom.2008.02.041,0.00276,-255,1.65,Ti1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,4.552,75.09,236400,1861,1579,208.21,17.351,12,362,0.00236,65100,0.136\r\n10.1016/j.jallcom.2008.02.041,0.00128,-211,2.45,Ti0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,4.818,75.24,236100,1890,1609,208.21,17.351,12,784,0.0035,44600,0.278\r\n10.1016/j.jallcom.2008.02.041,0.000908,-189,2.74,Ti0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,5.085,75.39,235900,1918,1638,208.21,17.351,12,1100,0.00392,35500,0.37\r\n10.1016/j.jallcom.2008.02.041,0.000567,-146,2.64,Ti0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,5.252,75.84,235200,2004,1726,208.21,17.351,12,1760,0.00377,21300,0.574\r\n10.1016/j.jallcom.2008.02.041,0.0028,-285,2.03,Zr1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,5.985,89.54,200100,2519,1929,226.87,18.906,12,357,0.0029,81000,0.102\r\n10.1016/j.jallcom.2008.02.041,0.00135,-228,2.71,Zr0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,6.052,89.55,200200,2537,1950,226.87,18.906,12,741,0.00387,52200,0.209\r\n10.1016/j.jallcom.2008.02.041,0.000874,-194,3,Zr0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,6.452,89.55,200400,2554,1972,226.87,18.906,12,1140,0.00429,37500,0.303\r\n10.1016/j.jallcom.2008.02.041,0.000474,-129,2.47,Zr0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,700,6.668,89.57,200900,2608,2036,226.87,18.906,12,2110,0.00353,16700,0.541\r\n10.1016/j.jallcom.2008.02.041,0.00163,-160,1.57,Ti1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,6.442,75.09,236400,1861,1579,208.21,17.351,12,615,0.00157,25500,0.233\r\n10.1016/j.jallcom.2008.02.041,0.00114,-173,2.61,Ti0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,6.292,75.24,236100,1890,1609,208.21,17.351,12,875,0.00261,29800,0.339\r\n10.1016/j.jallcom.2008.02.041,0.00096,-174,3.16,Ti0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,5.975,75.39,235900,1918,1638,208.21,17.351,12,1040,0.00316,30400,0.425\r\n10.1016/j.jallcom.2008.02.041,0.000726,-143,2.8,Ti0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,5.492,75.84,235200,2004,1726,208.21,17.351,12,1380,0.0028,20300,0.612\r\n10.1016/j.jallcom.2008.02.041,0.00159,-213,2.85,Zr1Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,6.642,89.54,200100,2519,1929,226.87,18.906,12,629,0.00285,45300,0.231\r\n10.1016/j.jallcom.2008.02.041,0.00121,-211,3.66,Zr0.99Nb0.01Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,6.062,89.55,200200,2537,1950,226.87,18.906,12,823,0.00366,44400,0.331\r\n10.1016/j.jallcom.2008.02.041,0.000952,-196,4.05,Zr0.98Nb0.02Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,6.208,89.55,200400,2554,1972,226.87,18.906,12,1050,0.00405,38500,0.413\r\n10.1016/j.jallcom.2008.02.041,0.000587,-151,3.87,Zr0.95Nb0.05Ni1Sn1,\"arc-melted, vacuum\",polycrystalline,1000,6.242,89.57,200900,2608,2036,226.87,18.906,12,1700,0.00387,22700,0.667\r\n10.1016/j.jallcom.2009.08.012,5.008,-572,0.00196,Ca1Mn1O3,Solid state reaction,polycrystalline,300,,28.6,398,1861,1276,206.97,10.348,20,0.2,6.53E-06,327000,\r\n10.1016/j.jallcom.2009.08.012,0.02,-100,0.01,Ca0.98Bi0.02Mn0.98Nb0.02O3,Solid state reaction,polycrystalline,300,2.513,29.43,1672000,2034,1500,206.97,10.348,20,49.2,4.92E-05,10000,0.014\r\n10.1016/j.jallcom.2009.08.012,0.00886,-91,0.03,Ca0.96Bi0.04Mn0.96Nb0.04O3,Solid state reaction,polycrystalline,300,2.268,30.26,3252000,2198,1711,206.97,10.348,20,113,9.38E-05,8310,0.036\r\n10.1016/j.jallcom.2009.08.012,0.00733,-72,0.02,Ca0.9Bi0.1Mn0.9Nb0.1O3,Solid state reaction,polycrystalline,300,,32.74,7513000,2638,2282,206.97,10.348,20,137,7.12E-05,5220,\r\n10.1016/j.jallcom.2009.08.012,2.925,-549,0.00412,Ca1Mn1O3,Solid state reaction,polycrystalline,400,3.306,28.6,398,1861,1276,206.97,10.348,20,0.342,1.03E-05,302000,0.000101\r\n10.1016/j.jallcom.2009.08.012,0.022,-119,0.03,Ca0.98Bi0.02Mn0.98Nb0.02O3,Solid state reaction,polycrystalline,400,2.275,29.43,1672000,2034,1500,206.97,10.348,20,46.4,6.60E-05,14200,0.02\r\n10.1016/j.jallcom.2009.08.012,0.00982,-114,0.05,Ca0.96Bi0.04Mn0.96Nb0.04O3,Solid state reaction,polycrystalline,400,2.16,30.26,3252000,2198,1711,206.97,10.348,20,102,0.000133,13000,0.046\r\n10.1016/j.jallcom.2009.08.012,0.00726,-72,0.03,Ca0.9Bi0.1Mn0.9Nb0.1O3,Solid state reaction,polycrystalline,400,,32.74,7513000,2638,2282,206.97,10.348,20,138,7.23E-05,5250,\r\n10.1016/j.jallcom.2009.08.012,0.643,-477,0.02,Ca1Mn1O3,Solid state reaction,polycrystalline,700,2.047,28.6,398,1861,1276,206.97,10.348,20,1.555,3.54E-05,228000,0.0013\r\n10.1016/j.jallcom.2009.08.012,0.026,-184,0.09,Ca0.98Bi0.02Mn0.98Nb0.02O3,Solid state reaction,polycrystalline,700,1.878,29.43,1672000,2034,1500,206.97,10.348,20,38.6,0.000131,34000,0.035\r\n10.1016/j.jallcom.2009.08.012,0.013,-164,0.15,Ca0.96Bi0.04Mn0.96Nb0.04O3,Solid state reaction,polycrystalline,700,1.878,30.26,3252000,2198,1711,206.97,10.348,20,80,0.000215,26900,0.073\r\n10.1016/j.jallcom.2009.08.012,0.00763,-81,0.06,Ca0.9Bi0.1Mn0.9Nb0.1O3,Solid state reaction,polycrystalline,700,,32.74,7513000,2638,2282,206.97,10.348,20,131,8.52E-05,6500,\r\n10.1016/j.jallcom.2009.08.012,0.111,-407,0.15,Ca1Mn1O3,Solid state reaction,polycrystalline,1000,1.679,28.6,398,1861,1276,206.97,10.348,20,9.044,0.00015,165000,0.013\r\n10.1016/j.jallcom.2009.08.012,0.027,-205,0.16,Ca0.98Bi0.02Mn0.98Nb0.02O3,Solid state reaction,polycrystalline,1000,1.736,29.43,1672000,2034,1500,206.97,10.348,20,37.5,0.000158,42100,0.053\r\n10.1016/j.jallcom.2009.08.012,0.015,-172,0.2,Ca0.9Bi0.1Mn0.9Nb0.1O3,Solid state reaction,polycrystalline,1000,1.687,32.74,7513000,2638,2282,206.97,10.348,20,68.7,0.000204,29700,0.099\r\n10.1016/j.jallcom.2009.08.012,0.0083,-93,0.1,Ca0.9Bi0.1Mn0.9Nb0.1O3,Solid state reaction,polycrystalline,1000,,32.74,7513000,2638,2282,206.97,10.348,20,120,0.000103,8590,\r\n10.1016/j.jallcom.2010.06.195,5.017,-40,9.35E-06,Sr1Nb0.15Ti0.85O3,\"solid state reaction, Ar\",polycrystalline,300,5.88,38.05,5257,2915,2484,60.64,12.128,5,0.199,3.12E-08,1560,2.48E-05\r\n10.1016/j.jallcom.2010.06.195,0.375,-48,0.000241,Sr1Nb0.15Ti0.85O3,\"solid state reaction, Ar\",polycrystalline,400,4.696,38.05,5257,2915,2484,60.64,12.128,5,2.663,6.02E-07,2260,0.000554\r\n10.1016/j.jallcom.2010.06.195,0.055,-100,0.01,Sr1Nb0.15Ti0.85O3,\"solid state reaction, Ar\",polycrystalline,700,3.49,38.05,5257,2915,2484,60.64,12.128,5,18.1,1.81E-05,10000,0.00887\r\n10.1016/j.jallcom.2010.06.195,0.024,-177,0.13,Sr1Nb0.15Ti0.85O3,\"solid state reaction, Ar\",polycrystalline,1000,3.078,38.05,5257,2915,2484,60.64,12.128,5,40.9,0.000128,31200,0.032\r\n10.1016/j.jcrysgro.2006.10.270,0.00122,-178,0.78,Mg2Si1,\"Bridgman method, Ar-H gas\",polycrystalline,300,7.25,25.57,27.34,5057,683.1,258.55,21.546,12,821,0.0026,31700,0.083\r\n10.1016/j.jcrysgro.2006.10.270,0.00173,-205,0.97,Mg2Si1,\"Bridgman method, Ar-H gas\",polycrystalline,400,6.15,25.57,27.34,5057,683.1,258.55,21.546,12,578,0.00243,42000,0.092\r\n10.1016/j.jcrysgro.2006.10.270,0.00412,-283,1.36,Mg2Si1,\"Bridgman method, Ar-H gas\",polycrystalline,700,3.05,25.57,27.34,5057,683.1,258.55,21.546,12,242,0.00194,79900,0.136\r\n10.1016/j.jeurceramsoc.2006.04.012,0.085,-160,0.02,Zn1O1,\"solid state reaction, air\",polycrystalline,700,,40.69,10780,1363,1621,47.62,11.905,4,11.8,3.01E-05,25600,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.068,-134,0.02,Zn0.98Al0.02O1,\"solid state reaction, air\",polycrystalline,700,,40.31,10670,1361,1612,47.62,11.905,4,14.7,2.62E-05,17900,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.05,-125,0.02,Zn0.97Al0.03O1,\"solid state reaction, air\",polycrystalline,700,,40.11,10610,1360,1608,47.62,11.905,4,20.1,3.14E-05,15600,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.047,-113,0.02,Zn0.95Al0.05O1,\"solid state reaction, air\",polycrystalline,700,,39.73,10490,1358,1599,47.62,11.905,4,21.4,2.71E-05,12700,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.034,-171,0.06,Zn0.97Al0.025Ti0.005O1,\"solid state reaction, air\",polycrystalline,700,,40.17,10600,1359,1609,47.62,11.905,4,29.6,8.62E-05,29200,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.029,-148,0.05,Zn0.97Al0.02Ti0.01O1,\"solid state reaction, air\",polycrystalline,700,,40.22,10580,1358,1609,47.62,11.905,4,34,7.45E-05,21900,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.026,-143,0.06,Zn0.97Al0.015Ti0.015O1,\"solid state reaction, air\",polycrystalline,700,,40.27,10570,1357,1610,47.62,11.905,4,38.5,7.88E-05,20500,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.024,-139,0.06,Zn0.97Al0.01Ti0.02O1,\"solid state reaction, air\",polycrystalline,700,,40.32,10560,1356,1611,47.62,11.905,4,42.5,8.22E-05,19300,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.061,-191,0.06,Zn1O1,\"solid state reaction, air\",polycrystalline,1000,,40.69,10780,1363,1621,47.62,11.905,4,16.5,6.02E-05,36500,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.025,-182,0.13,Zn0.98Al0.02O1,\"solid state reaction, air\",polycrystalline,1000,,40.31,10670,1361,1612,47.62,11.905,4,39.3,0.00013,33100,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.019,-174,0.16,Zn0.97Al0.03O1,\"solid state reaction, air\",polycrystalline,1000,,40.11,10610,1360,1608,47.62,11.905,4,51.6,0.000155,30100,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.018,-164,0.15,Zn0.95Al0.05O1,\"solid state reaction, air\",polycrystalline,1000,,39.73,10490,1358,1599,47.62,11.905,4,54.6,0.000148,27000,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.017,-217,0.27,Zn0.97Al0.025Ti0.005O1,\"solid state reaction, air\",polycrystalline,1000,,40.17,10600,1359,1609,47.62,11.905,4,57.5,0.000271,47200,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.016,-212,0.28,Zn0.97Al0.02Ti0.01O1,\"solid state reaction, air\",polycrystalline,1000,,40.22,10580,1358,1609,47.62,11.905,4,62.9,0.000283,45100,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.014,-205,0.29,Zn0.97Al0.015Ti0.015O1,\"solid state reaction, air\",polycrystalline,1000,,40.27,10570,1357,1610,47.62,11.905,4,69.2,0.000292,42200,\r\n10.1016/j.jeurceramsoc.2006.04.012,0.013,-195,0.29,Zn0.97Al0.01Ti0.02O1,\"solid state reaction, air\",polycrystalline,1000,,40.32,10560,1356,1611,47.62,11.905,4,75.5,0.000287,38100,\r\n10.1016/j.jpcs.2004.01.010,0.000161,-81,1.23,Bi92Sb8,\"melted, vacuum\",polcrystalline,300,,202,56230000,5422,5869,195.59,32.598,6,6220,0.00411,6620,\r\n10.1016/j.jpcs.2004.01.010,0.000182,-81,1.07,Bi90Sb10,\"melted, vacuum\",polcrystalline,300,,200.26,55550000,5455,5836,195.59,32.598,6,5490,0.00358,6520,\r\n10.1016/j.jpcs.2004.01.010,0.000172,-85,1.27,Bi88Sb12,\"melted, vacuum\",polcrystalline,300,,198.51,54860000,5488,5804,195.59,32.598,6,5810,0.00423,7270,\r\n10.1016/j.jpcs.2004.01.010,0.000256,-81,0.77,Bi86Sb14,\"melted, vacuum\",polcrystalline,300,,196.77,54160000,5522,5770,195.59,32.598,6,3900,0.00258,6620,\r\n10.1016/j.jpcs.2004.01.010,0.00026,-75,0.65,Bi83Sb17,\"melted, vacuum\",polcrystalline,300,,194.15,53090000,5574,5719,195.59,32.598,6,3850,0.00218,5660,\r\n10.1016/j.jpcs.2004.01.010,0.000155,-69,1.24,Bi92Sb8,\"melted, vacuum\",polcrystalline,400,,202,56230000,5422,5869,195.59,32.598,6,6430,0.00309,4800,\r\n10.1016/j.jpcs.2004.01.010,0.000181,-69,1.04,Bi90Sb10,\"melted, vacuum\",polcrystalline,400,,200.26,55550000,5455,5836,195.59,32.598,6,5530,0.0026,4690,\r\n10.1016/j.jpcs.2004.01.010,0.000168,-73,1.26,Bi88Sb12,\"melted, vacuum\",polcrystalline,400,,198.51,54860000,5488,5804,195.59,32.598,6,5960,0.00316,5310,\r\n10.1016/j.jpcs.2004.01.010,0.000293,-69,0.65,Bi86Sb14,\"melted, vacuum\",polcrystalline,400,,196.77,54160000,5522,5770,195.59,32.598,6,3420,0.00163,4780,\r\n10.1016/j.jpcs.2004.01.010,0.000285,-62,0.53,Bi83Sb17,\"melted, vacuum\",polcrystalline,400,,194.15,53090000,5574,5719,195.59,32.598,6,3510,0.00133,3790,\r\n10.1016/j.jssc.2008.08.078,7.718,-390,0.000591,La1Co1O3,solid state reaction,polycrystalline,300,1.879,49.17,24200,6184,2502,222.73,11.136,20,0.13,1.97E-06,152000,5.05E-05\r\n10.1016/j.jssc.2008.08.078,0.157,395,0.03,La0.99Sr0.01Co1O3,solid state reaction,polycrystalline,300,1.807,49.06,24100,6158,2500,222.73,11.136,20,6.368,9.94E-05,156000,0.00258\r\n10.1016/j.jssc.2008.08.078,0.069,330,0.05,La0.98Sr0.02Co1O3,solid state reaction,polycrystalline,300,1.8,48.96,24010,6132,2499,222.73,11.136,20,14.5,0.000157,109000,0.00588\r\n10.1016/j.jssc.2008.08.078,0.016,215,0.09,La0.95Sr0.05Co1O3,solid state reaction,polycrystalline,300,1.8,48.65,23720,6053,2493,222.95,11.147,20,62.7,0.000289,46100,0.025\r\n10.1016/j.jssc.2008.08.078,0.000468,21,0.03,La0.8Sr0.2Co1O3,solid state reaction,polycrystalline,300,3.696,47.12,22220,5646,2465,224.2,11.21,20,2140,9.72E-05,455,0.423\r\n10.1016/j.jssc.2008.08.078,0.384,140,0.00205,La1Co1O3,solid state reaction,polycrystalline,400,,49.17,24200,6184,2502,222.73,11.136,20,2.605,5.13E-06,19700,\r\n10.1016/j.jssc.2008.08.078,0.074,304,0.05,La0.99Sr0.01Co1O3,solid state reaction,polycrystalline,400,,49.06,24100,6158,2500,222.73,11.136,20,13.5,0.000125,92400,\r\n10.1016/j.jssc.2008.08.078,0.034,244,0.07,La0.98Sr0.02Co1O3,solid state reaction,polycrystalline,400,,48.96,24010,6132,2499,222.73,11.136,20,29.6,0.000175,59300,\r\n10.1016/j.jssc.2008.08.078,0.00728,129,0.09,La0.95Sr0.05Co1O3,solid state reaction,polycrystalline,400,,48.65,23720,6053,2493,222.95,11.147,20,137,0.000229,16600,\r\n10.1016/j.jssc.2008.08.078,0.000447,18,0.03,La0.8Sr0.2Co1O3,solid state reaction,polycrystalline,400,,47.12,22220,5646,2465,224.2,11.21,20,2240,6.93E-05,310,\r\n10.1016/j.jssc.2008.08.078,0.00136,29,0.04,La1Co1O3,solid state reaction,polycrystalline,700,,49.17,24200,6184,2502,222.73,11.136,20,736,6.09E-05,827,\r\n10.1016/j.jssc.2008.08.078,0.00123,32,0.06,La0.99Sr0.01Co1O3,solid state reaction,polycrystalline,700,,49.06,24100,6158,2500,222.73,11.136,20,813,8.57E-05,1050,\r\n10.1016/j.jssc.2008.08.078,0.0011,29,0.05,La0.98Sr0.02Co1O3,solid state reaction,polycrystalline,700,,48.96,24010,6132,2499,222.73,11.136,20,912,7.54E-05,827,\r\n10.1016/j.jssc.2008.08.078,0.00095,25,0.05,La0.95Sr0.05Co1O3,solid state reaction,polycrystalline,700,,48.65,23720,6053,2493,222.95,11.147,20,1050,6.60E-05,627,\r\n10.1016/j.jssc.2008.08.078,0.000499,10,0.01,La0.8Sr0.2Co1O3,solid state reaction,polycrystalline,700,,47.12,22220,5646,2465,224.2,11.21,20,2000,2.07E-05,103,\r\n10.1016/j.jssc.2008.08.078,0.000984,16,0.03,La1Co1O3,solid state reaction,polycrystalline,1000,,49.17,24200,6184,2502,222.73,11.136,20,1020,2.50E-05,246,\r\n10.1016/j.jssc.2008.08.078,0.000951,19,0.04,La0.99Sr0.01Co1O3,solid state reaction,polycrystalline,1000,,49.06,24100,6158,2500,222.73,11.136,20,1050,3.62E-05,344,\r\n10.1016/j.jssc.2008.08.078,0.000916,18,0.03,La0.98Sr0.02Co1O3,solid state reaction,polycrystalline,1000,,48.96,24010,6132,2499,222.73,11.136,20,1090,3.38E-05,310,\r\n10.1016/j.jssc.2008.08.078,0.000832,15,0.03,La0.95Sr0.05Co1O3,solid state reaction,polycrystalline,1000,,48.65,23720,6053,2493,222.95,11.147,20,1200,2.63E-05,219,\r\n10.1016/j.jssc.2008.08.078,0.000597,6,0.0051,La0.8Sr0.2Co1O3,solid state reaction,polycrystalline,1000,,47.12,22220,5646,2465,224.2,11.21,20,1670,5.10E-06,30.5,\r\n10.1016/j.jssc.2011.02.027,0.000588,-27,0.04,Ba7Sr1Al16Si30,\"flux (Al), dynamic vacuum\",polycrystalline,300,2.31,43.02,1088,3387,1633,1193,21.691,55,1700,0.00012,703,0.539\r\n10.1016/j.jssc.2011.02.027,0.00066,-34,0.07,Ba7Sr1Al16Si30,\"flux (Al), dynamic vacuum\",polycrystalline,400,2.33,43.02,1088,3387,1633,1193,21.691,55,1510,0.000172,1140,0.634\r\n10.1016/j.jssc.2011.02.027,0.000878,-53,0.23,Ba7Sr1Al16Si30,\"flux (Al), dynamic vacuum\",polycrystalline,700,2.46,43.02,1088,3387,1633,1193,21.691,55,1140,0.000322,2830,0.791\r\n10.1016/j.jssc.2011.02.027,0.00112,-79,0.56,Ba7Sr1Al16Si30,\"flux (Al), dynamic vacuum\",polycrystalline,1000,2.57,43.02,1088,3387,1633,1193,21.691,55,895,0.000559,6250,0.85\r\n10.1016/j.progsolidstchem.2007.01.027,0.026,-81,0.00756,Sr1Mn0.98Mo0.02O3,\"solid state reaction, air\",polycrystalline,300,,38.28,10260,2511,2055,234.85,11.742,20,38.8,2.52E-05,6490,\r\n10.1016/j.progsolidstchem.2007.01.027,0.015,-110,0.02,Sr1Mn0.96Mo0.04O3,\"solid state reaction, air\",polycrystalline,300,,38.44,18890,2515,2089,234.85,11.742,20,64.9,7.90E-05,12200,\r\n10.1016/j.progsolidstchem.2007.01.027,0.026,-74,0.00837,Sr1Mn0.98Mo0.02O3,\"solid state reaction, air\",polycrystalline,400,,38.28,10260,2511,2055,234.85,11.742,20,38.4,2.09E-05,5450,\r\n10.1016/j.progsolidstchem.2007.01.027,0.015,-105,0.03,Sr1Mn0.96Mo0.04O3,\"solid state reaction, air\",polycrystalline,400,,38.44,18890,2515,2089,234.85,11.742,20,65.9,7.27E-05,11000,\r\n10.1016/j.progsolidstchem.2007.01.027,0.034,-58,0.0071,Sr1Mn0.98Mo0.02O3,\"solid state reaction, air\",polycrystalline,700,,38.28,10260,2511,2055,234.85,11.742,20,29.8,1.01E-05,3400,\r\n10.1016/j.progsolidstchem.2007.01.027,0.017,-89,0.03,Sr1Mn0.96Mo0.04O3,\"solid state reaction, air\",polycrystalline,700,,38.44,18890,2515,2089,234.85,11.742,20,57.5,4.51E-05,7850,\r\n10.1016/j.progsolidstchem.2007.01.027,0.036,-40,0.00454,Sr1Mn0.98Mo0.02O3,\"solid state reaction, air\",polycrystalline,1000,,38.28,10260,2511,2055,234.85,11.742,20,28.1,4.54E-06,1610,\r\n10.1016/j.progsolidstchem.2007.01.027,0.023,-74,0.02,Sr1Mn0.96Mo0.04O3,\"solid state reaction, air\",polycrystalline,1000,,38.44,18890,2515,2089,234.85,11.742,20,43.6,2.41E-05,5530,\r\n10.1016/j.ssc.2007.12.033,0.014,-156,0.05,In2O3,solid state reaction,polycrystalline,300,9.67,55.53,4035000,2843,1741,1035.51,12.944,80,74,0.00018,24400,0.0056\r\n10.1016/j.ssc.2007.12.033,0.00211,-89,0.11,In1.998Ge0.002O3,solid state reaction,polycrystalline,300,9.156,55.51,4032000,2844,1741,1035.51,12.944,80,475,0.000373,7840,0.038\r\n10.1016/j.ssc.2007.12.033,0.000837,-50,0.09,In1.994Ge0.006O3,solid state reaction,polycrystalline,300,9.715,55.48,4027000,2846,1740,1035.51,12.944,80,1200,0.000304,2550,0.09\r\n10.1016/j.ssc.2007.12.033,0.000723,-47,0.09,In1.985Ge0.015O3,solid state reaction,polycrystalline,300,9.419,55.4,4016000,2850,1740,1035.51,12.944,80,1380,0.000302,2190,0.107\r\n10.1016/j.ssc.2007.12.033,0.000896,-51,0.09,In1.94Ge0.06O3,solid state reaction,polycrystalline,300,8.868,55.02,3961000,2869,1737,1035.51,12.944,80,1120,0.000288,2580,0.092\r\n10.1016/j.ssc.2007.12.033,0.00132,-53,0.06,In1.9Ge0.1O3,solid state reaction,polycrystalline,300,6.847,54.68,3910000,2887,1734,1035.51,12.944,80,757,0.000215,2840,0.081\r\n10.1016/j.ssc.2007.12.033,0.00287,-52,0.03,In1.8Ge0.2O3,solid state reaction,polycrystalline,300,3.238,53.84,3782000,2932,1727,1035.51,12.944,80,348,9.53E-05,2740,0.079\r\n10.1016/j.ssc.2007.12.033,0.015,-173,0.08,In2O3,solid state reaction,polycrystalline,400,6.773,55.53,4035000,2843,1741,1035.51,12.944,80,66.9,0.0002,29800,0.00964\r\n10.1016/j.ssc.2007.12.033,0.00235,-106,0.19,In1.998Ge0.002O3,solid state reaction,polycrystalline,400,6.853,55.51,4032000,2844,1741,1035.51,12.944,80,426,0.000477,11200,0.061\r\n10.1016/j.ssc.2007.12.033,0.000942,-62,0.17,In1.994Ge0.006O3,solid state reaction,polycrystalline,400,7.207,55.48,4027000,2846,1740,1035.51,12.944,80,1060,0.000414,3900,0.144\r\n10.1016/j.ssc.2007.12.033,0.000818,-57,0.16,In1.985Ge0.015O3,solid state reaction,polycrystalline,400,7.048,55.4,4016000,2850,1740,1035.51,12.944,80,1220,0.000392,3200,0.169\r\n10.1016/j.ssc.2007.12.033,0.000995,-61,0.15,In1.94Ge0.06O3,solid state reaction,polycrystalline,400,6.604,55.02,3961000,2869,1737,1035.51,12.944,80,1000,0.000369,3670,0.148\r\n10.1016/j.ssc.2007.12.033,0.00143,-66,0.12,In1.9Ge0.1O3,solid state reaction,polycrystalline,400,5.091,54.68,3910000,2887,1734,1035.51,12.944,80,697,0.0003,4300,0.134\r\n10.1016/j.ssc.2007.12.033,0.0028,-64,0.06,In1.8Ge0.2O3,solid state reaction,polycrystalline,400,2.611,53.84,3782000,2932,1727,1035.51,12.944,80,358,0.000147,4100,0.134\r\n10.1016/j.ssc.2007.12.033,0.019,-202,0.15,In2O3,solid state reaction,polycrystalline,700,3.866,55.53,4035000,2843,1741,1035.51,12.944,80,51.3,0.00021,40900,0.023\r\n10.1016/j.ssc.2007.12.033,0.00337,-146,0.44,In1.998Ge0.002O3,solid state reaction,polycrystalline,700,3.923,55.51,4032000,2844,1741,1035.51,12.944,80,297,0.000634,21400,0.129\r\n10.1016/j.ssc.2007.12.033,0.00129,-94,0.48,In1.994Ge0.006O3,solid state reaction,polycrystalline,700,4.584,55.48,4027000,2846,1740,1035.51,12.944,80,774,0.000686,8860,0.288\r\n10.1016/j.ssc.2007.12.033,0.00113,-83,0.43,In1.985Ge0.015O3,solid state reaction,polycrystalline,700,4.619,55.4,4016000,2850,1740,1035.51,12.944,80,884,0.000613,6940,0.327\r\n10.1016/j.ssc.2007.12.033,0.0014,-89,0.39,In1.94Ge0.06O3,solid state reaction,polycrystalline,700,3.9,55.02,3961000,2869,1737,1035.51,12.944,80,716,0.000562,7840,0.314\r\n10.1016/j.ssc.2007.12.033,0.00173,-93,0.35,In1.9Ge0.1O3,solid state reaction,polycrystalline,700,3.244,54.68,3910000,2887,1734,1035.51,12.944,80,578,0.000502,8690,0.304\r\n10.1016/j.ssc.2007.12.033,0.00244,-86,0.21,In1.8Ge0.2O3,solid state reaction,polycrystalline,700,1.836,53.84,3782000,2932,1727,1035.51,12.944,80,410,0.000306,7460,0.382\r\n10.1016/j.ssc.2007.12.033,0.023,-223,0.22,In2O3,solid state reaction,polycrystalline,1000,2.976,55.53,4035000,2843,1741,1035.51,12.944,80,43.5,0.000216,49600,0.036\r\n10.1016/j.ssc.2007.12.033,0.0045,-178,0.7,In1.998Ge0.002O3,solid state reaction,polycrystalline,1000,2.931,55.51,4032000,2844,1741,1035.51,12.944,80,222,0.000703,31600,0.185\r\n10.1016/j.ssc.2007.12.033,0.00168,-119,0.85,In1.994Ge0.006O3,solid state reaction,polycrystalline,1000,3.49,55.48,4027000,2846,1740,1035.51,12.944,80,594,0.000846,14200,0.415\r\n10.1016/j.ssc.2007.12.033,0.00143,-108,0.82,In1.985Ge0.015O3,solid state reaction,polycrystalline,1000,3.536,55.4,4016000,2850,1740,1035.51,12.944,80,697,0.00082,11800,0.481\r\n10.1016/j.ssc.2007.12.033,0.00178,-115,0.74,In1.94Ge0.06O3,solid state reaction,polycrystalline,1000,3.063,55.02,3961000,2869,1737,1035.51,12.944,80,562,0.000743,13200,0.448\r\n10.1016/j.ssc.2007.12.033,0.00209,-117,0.66,In1.9Ge0.1O3,solid state reaction,polycrystalline,1000,2.514,54.68,3910000,2887,1734,1035.51,12.944,80,479,0.000661,13800,0.465\r\n10.1016/j.ssc.2007.12.033,0.00267,-110,0.45,In1.8Ge0.2O3,solid state reaction,polycrystalline,1000,1.631,53.84,3782000,2932,1727,1035.51,12.944,80,374,0.000453,12100,0.56\r\n10.1016/j.ssc.2012.03.013,0.0032,130,0.16,La1.61Sr0.39Cu0.94Ti0.06O4,Solid state reaction,polycrystalline,300,,54.92,18610,6221,2419,188.19,13.442,14,312,0.000528,16900,\r\n10.1016/j.ssc.2012.03.013,12.6,200,9.52E-05,La1.85Sr0.15Cu0.94Ti0.06O4,Solid state reaction,polycrystalline,300,,56.67,20190,6603,2448,189.68,13.549,14,0.079,3.17E-07,40000,\r\n10.1016/j.ssc.2012.03.013,0.0039,20,0.00308,La1.73Sr0.27Cu0.94Ti0.06O4,Solid state reaction,polycrystalline,300,,55.79,19410,6415,2433,188.56,13.469,14,256,1.03E-05,400,\r\n10.1016/j.ssc.2012.03.013,0.0035,5,0.000214,La1.69Sr0.31Cu0.94Ti0.06O4,Solid state reaction,polycrystalline,300,,55.5,19150,6351,2429,188.45,13.461,14,286,7.14E-07,25,\r\n10.1016/j.ssc.2012.03.013,0.0032,6,0.000372,La1.67Sr0.34Cu0.94Ti0.06O4,Solid state reaction,polycrystalline,300,,55.4,18980,6314,2427,188.41,13.458,14,312,1.24E-06,39.7,\r\n10.1016/S0022-3697(96)00228-4,0.00211,111,0.18,Zn4Sb3,\"melted, inert\",polycrystalline,300,1.01,89.54,2919000,5264,2783,1610.64,25.566,63,475,0.000583,12300,0.344\r\n10.1016/S0022-3697(96)00228-4,0.00259,146,0.33,Zn4Sb3,\"melted, inert\",polycrystalline,400,0.664,89.54,2919000,5264,2783,1610.64,25.566,63,386,0.000823,21300,0.568\r\n10.1016/S0022-3697(96)00228-4,0.00333,206,0.89,Zn4Sb3,\"melted, inert\",polycrystalline,700,0.693,89.54,2919000,5264,2783,1610.64,25.566,63,301,0.00127,42400,0.741\r\n10.1016/S0025-5408(02)00997-2,0.018,-154,0.05,Ca1Mn0.98Ru0.02O3,Solid state reaction,polycrystalline,400,,28.79,14040000,1883,1366,208.21,10.41,20,54.4,0.000129,23600,\r\n10.1016/S0025-5408(02)00997-2,0.00752,-120,0.08,Ca1Mn0.96Ru0.04O3,Solid state reaction,polycrystalline,400,3.758,28.97,27910000,1904,1456,208.21,10.41,20,133,0.000191,14400,0.035\r\n10.1016/S0025-5408(02)00997-2,0.0066,-102,0.06,Ca1Mn0.94Ru0.06O3,Solid state reaction,polycrystalline,400,,29.16,41600000,1925,1544,208.21,10.41,20,151,0.000156,10300,\r\n10.1016/S0025-5408(02)00997-2,0.00396,-61,0.04,Ca1Mn0.9Ru0.1O3,Solid state reaction,polycrystalline,400,,29.53,68460000,1966,1717,210.36,10.518,20,253,9.27E-05,3670,\r\n10.1016/S0025-5408(02)00997-2,0.00311,-36,0.02,Ca1Mn0.82Ru0.18O3,Solid state reaction,polycrystalline,400,,30.26,120200000,2045,2051,210.36,10.518,20,322,4.10E-05,1270,\r\n10.1016/S0025-5408(02)00997-2,0.024,-196,0.11,Ca1Mn0.98Ru0.02O3,Solid state reaction,polycrystalline,700,,28.79,14040000,1883,1366,208.21,10.41,20,41.4,0.000159,38300,\r\n10.1016/S0025-5408(02)00997-2,0.01,-137,0.13,Ca1Mn0.96Ru0.04O3,Solid state reaction,polycrystalline,700,3.24,28.97,27910000,1904,1456,208.21,10.41,20,98.2,0.000185,18800,0.052\r\n10.1016/S0025-5408(02)00997-2,0.00892,-122,0.12,Ca1Mn0.94Ru0.06O3,Solid state reaction,polycrystalline,700,,29.16,41600000,1925,1544,208.21,10.41,20,112,0.000167,14900,\r\n10.1016/S0025-5408(02)00997-2,0.00529,-82,0.09,Ca1Mn0.9Ru0.1O3,Solid state reaction,polycrystalline,700,,29.53,68460000,1966,1717,210.36,10.518,20,189,0.000126,6660,\r\n10.1016/S0025-5408(02)00997-2,0.00403,-56,0.05,Ca1Mn0.82Ru0.18O3,Solid state reaction,polycrystalline,700,,30.26,120200000,2045,2051,210.36,10.518,20,248,7.75E-05,3120,\r\n10.1016/S0025-5408(02)00997-2,0.028,-214,0.16,Ca1Mn0.98Ru0.02O3,Solid state reaction,polycrystalline,1000,,28.79,14040000,1883,1366,208.21,10.41,20,35.7,0.000163,45700,\r\n10.1016/S0025-5408(02)00997-2,0.013,-153,0.18,Ca1Mn0.96Ru0.04O3,Solid state reaction,polycrystalline,1000,2.882,28.97,27910000,1904,1456,208.21,10.41,20,78.8,0.000184,23400,0.067\r\n10.1016/S0025-5408(02)00997-2,0.011,-145,0.18,Ca1Mn0.94Ru0.06O3,Solid state reaction,polycrystalline,1000,,29.16,41600000,1925,1544,208.21,10.41,20,87.8,0.000183,20900,\r\n10.1016/S0025-5408(02)00997-2,0.00674,-102,0.15,Ca1Mn0.9Ru0.1O3,Solid state reaction,polycrystalline,1000,,29.53,68460000,1966,1717,210.36,10.518,20,148,0.000154,10400,\r\n10.1016/S0025-5408(02)00997-2,0.00505,-68,0.09,Ca1Mn0.82Ru0.18O3,Solid state reaction,polycrystalline,1000,,30.26,120200000,2045,2051,210.36,10.518,20,198,9.13E-05,4610,\r\n10.1016/S0038-1098(02)00555-0,0.046,50,0.00164,Ca3Co4O9,\"sol-gel, air\",polycrystalline,300,,31.25,17150,2511,1757,147.11,10.865,13.54,21.8,5.48E-06,2510,\r\n10.1016/S0038-1098(02)00555-0,0.041,62,0.00284,La0.05Ca2.85Co3.8O8.55,\"sol-gel, air\",polycrystalline,300,,31.6,17300,2612,1776,147.11,10.865,13.54,24.5,9.47E-06,3860,\r\n10.1016/S0038-1098(02)00555-0,0.06,60,0.00179,La0.3Ca2.7Co4O9,\"sol-gel, air\",polycrystalline,300,,33.1,18350,3029,1870,147.11,10.865,13.54,16.8,5.98E-06,3570,\r\n10.1016/S0038-1098(02)00555-0,0.043,65,0.00297,La0.45Ca2.55Co4O9,\"sol-gel, air\",polycrystalline,300,,34.03,18900,3266,1923,147.11,10.865,13.54,23.2,9.90E-06,4270,\r\n10.1016/S0038-1098(02)00555-0,0.041,58,0.00328,Ca3Co4O9,\"sol-gel, air\",polycrystalline,400,,31.25,17150,2511,1757,147.11,10.865,13.54,24.4,8.20E-06,3360,\r\n10.1016/S0038-1098(02)00555-0,0.038,70,0.00518,La0.05Ca2.85Co3.8O8.55,\"sol-gel, air\",polycrystalline,400,,31.6,17300,2612,1776,147.11,10.865,13.54,26.4,1.30E-05,4900,\r\n10.1016/S0038-1098(02)00555-0,0.039,68,0.00485,La0.3Ca2.7Co4O9,\"sol-gel, air\",polycrystalline,400,,33.1,18350,3029,1870,147.11,10.865,13.54,25.9,1.21E-05,4690,\r\n10.1016/S0038-1098(02)00555-0,0.037,73,0.00574,La0.45Ca2.55Co4O9,\"sol-gel, air\",polycrystalline,400,,34.03,18900,3266,1923,147.11,10.865,13.54,26.8,1.43E-05,5340,\r\n10.1016/S0038-1098(02)00555-0,0.029,84,0.02,Ca3Co4O9,\"sol-gel, air\",polycrystalline,700,,31.25,17150,2511,1757,147.11,10.865,13.54,34.8,2.47E-05,7100,\r\n10.1016/S0038-1098(02)00555-0,0.025,89,0.02,La0.05Ca2.85Co3.8O8.55,\"sol-gel, air\",polycrystalline,700,,31.6,17300,2612,1776,147.11,10.865,13.54,39.8,3.12E-05,7850,\r\n10.1016/S0038-1098(02)00555-0,0.021,92,0.03,La0.3Ca2.7Co4O9,\"sol-gel, air\",polycrystalline,700,,33.1,18350,3029,1870,147.11,10.865,13.54,48.3,4.13E-05,8540,\r\n10.1016/S0038-1098(02)00555-0,0.023,95,0.03,La0.45Ca2.55Co4O9,\"sol-gel, air\",polycrystalline,700,,34.03,18900,3266,1923,147.11,10.865,13.54,43.5,3.94E-05,9040,\r\n10.1016/S0038-1098(02)00555-0,0.026,119,0.05,Ca3Co4O9,\"sol-gel, air\",polycrystalline,1000,,31.25,17150,2511,1757,147.11,10.865,13.54,38.4,5.40E-05,14100,\r\n10.1016/S0038-1098(02)00555-0,0.019,124,0.08,La0.05Ca2.85Co3.8O8.55,\"sol-gel, air\",polycrystalline,1000,,31.6,17300,2612,1776,147.11,10.865,13.54,52.4,8.04E-05,15400,\r\n10.1016/S0038-1098(02)00555-0,0.015,127,0.11,La0.3Ca2.7Co4O9,\"sol-gel, air\",polycrystalline,1000,,33.1,18350,3029,1870,147.11,10.865,13.54,66.5,0.000107,16100,\r\n10.1016/S0038-1098(02)00555-0,0.018,132,0.1,La0.45Ca2.55Co4O9,\"sol-gel, air\",polycrystalline,1000,,34.03,18900,3266,1923,147.11,10.865,13.54,56.8,9.86E-05,17300,\r\n10.1016/S0038-1098(03)00080-2,0.000491,-2,0.000218,Bi2Ru2O7,Solid state reaction,polycrystalline,400,,66.55,309700000,3994,5707,1090.63,12.394,88,1880,5.46E-07,2.681,\r\n10.1016/S0038-1098(03)00080-2,0.00101,21,0.02,Y0.5Bi1.5Ru2O7,Solid state reaction,polycrystalline,400,,61.1,328200000,4178,5460,1079.79,12.27,88,969,4.55E-05,461,\r\n10.1016/S0038-1098(03)00080-2,0.002,15,0.00478,Y1Bi1Ru2O7,Solid state reaction,polycrystalline,400,,55.64,350400000,4398,5165,1069.75,12.156,88,502,1.20E-05,238,\r\n10.1016/S0038-1098(03)00080-2,5.732,270,0.000509,Y2Ru2O7,Solid state reaction,polycrystalline,400,,44.72,410900000,4999,4357,1040.8,11.827,88,0.173,1.27E-06,72900,\r\n10.1016/S0038-1098(03)00080-2,0.000574,5,0.00352,Bi2Ru2O7,Solid state reaction,polycrystalline,700,,66.55,309700000,3994,5707,1090.63,12.394,88,1730,5.03E-06,28.9,\r\n10.1016/S0038-1098(03)00080-2,0.00105,15,0.02,Y0.5Bi1.5Ru2O7,Solid state reaction,polycrystalline,700,,61.1,328200000,4178,5460,1079.79,12.27,88,946,2.22E-05,234,\r\n10.1016/S0038-1098(03)00080-2,0.0019,17,0.01,Y1Bi1Ru2O7,Solid state reaction,polycrystalline,700,,55.64,350400000,4398,5165,1069.75,12.156,88,515,1.55E-05,294,\r\n10.1016/S0038-1098(03)00080-2,0.284,22,0.000118,Y2Ru2O7,Solid state reaction,polycrystalline,700,,44.72,410900000,4999,4357,1040.8,11.827,88,3.465,1.69E-07,480,\r\n10.1016/S0038-1098(03)00080-2,0.000687,12,0.02,Bi2Ru2O7,Solid state reaction,polycrystalline,1000,,66.55,309700000,3994,5707,1090.63,12.394,88,1430,2.25E-05,155,\r\n10.1016/S0038-1098(03)00080-2,0.00119,17,0.03,Y0.5Bi1.5Ru2O7,Solid state reaction,polycrystalline,1000,,61.1,328200000,4178,5460,1079.79,12.27,88,830,2.50E-05,298,\r\n10.1016/S0038-1098(03)00080-2,0.002,17,0.01,Y1Bi1Ru2O7,Solid state reaction,polycrystalline,1000,,55.64,350400000,4398,5165,1069.75,12.156,88,492,1.48E-05,296,\r\n10.1016/S0038-1098(03)00080-2,0.084,17,0.000352,Y2Ru2O7,Solid state reaction,polycrystalline,1000,,44.72,410900000,4999,4357,1040.8,11.827,88,11.6,3.52E-07,298,\r\n10.1016/S0167-577X(01)00317-2,0.00176,23,0.01,Nd1.4Bi0.6Ru2O7,Solid state reaction,polycrystalline,400,,58.31,326600000,5126,4765,1102.66,12.53,88,569,3.03E-05,533,\r\n10.1016/S0167-577X(01)00317-2,0.00117,21,0.02,Nd1Bi1Ru2O7,Solid state reaction,polycrystalline,400,,60.67,321300000,4772,5060,1098.72,12.485,88,854,3.83E-05,448,\r\n10.1016/S0167-577X(01)00317-2,0.00322,18,0.0039,Yb1.4Bi0.6Ru2O7,Solid state reaction,polycrystalline,400,,61.98,307400000,5384,4668,1098.72,12.485,88,311,9.75E-06,314,\r\n10.1016/S0167-577X(01)00317-2,0.00169,19,0.0088,Yb1Bi1Ru2O7,Solid state reaction,polycrystalline,400,,63.29,308100000,4966,4980,1098.72,12.485,88,591,2.20E-05,372,\r\n10.1016/S0167-577X(01)00317-2,0.00193,32,0.04,Nd1.4Bi0.6Ru2O7,Solid state reaction,polycrystalline,700,,58.31,326600000,5126,4765,1102.66,12.53,88,519,5.46E-05,1050,\r\n10.1016/S0167-577X(01)00317-2,0.00134,30,0.05,Nd1Bi1Ru2O7,Solid state reaction,polycrystalline,700,,60.67,321300000,4772,5060,1098.72,12.485,88,746,6.83E-05,915,\r\n10.1016/S0167-577X(01)00317-2,0.0031,29,0.02,Yb1.4Bi0.6Ru2O7,Solid state reaction,polycrystalline,700,,61.98,307400000,5384,4668,1098.72,12.485,88,323,2.77E-05,860,\r\n10.1016/S0167-577X(01)00317-2,0.00177,29,0.03,Yb1Bi1Ru2O7,Solid state reaction,polycrystalline,700,,63.29,308100000,4966,4980,1098.72,12.485,88,565,4.86E-05,860,\r\n10.1016/S0167-577X(01)00317-2,0.00204,40,0.08,Nd1.4Bi0.6Ru2O7,Solid state reaction,polycrystalline,1000,,58.31,326600000,5126,4765,1102.66,12.53,88,491,7.84E-05,1600,\r\n10.1016/S0167-577X(01)00317-2,0.00153,35,0.08,Nd1Bi1Ru2O7,Solid state reaction,polycrystalline,1000,,60.67,321300000,4772,5060,1098.72,12.485,88,653,8.21E-05,1260,\r\n10.1016/S0167-577X(01)00317-2,0.00298,39,0.05,Yb1.4Bi0.6Ru2O7,Solid state reaction,polycrystalline,1000,,61.98,307400000,5384,4668,1098.72,12.485,88,336,5.10E-05,1520,\r\n10.1016/S0167-577X(01)00317-2,0.00181,36,0.07,Yb1Bi1Ru2O7,Solid state reaction,polycrystalline,1000,,63.29,308100000,4966,4980,1098.72,12.485,88,552,7.10E-05,1290,\r\n10.1016/S0925-8388(01)01804-7,0.888,-413,0.00577,Fe1.98Ti0.02O3,\"solid state reaction, air\",polycrystalline,300,,31.91,13.87,1837,1111,101.11,10.111,10,11300,1.92E-05,171000,\r\n10.1016/S0925-8388(01)01804-7,0.376,-366,0.01,Fe1.96Ti0.04O3,\"solid state reaction, air\",polycrystalline,300,7.82,31.87,14.74,1829,1112,101.11,10.111,10,26600,3.57E-05,134000,2.487\r\n10.1016/S0925-8388(01)01804-7,0.412,-335,0.00818,Fe1.94Ti0.06O3,\"solid state reaction, air\",polycrystalline,300,6.39,31.84,15.62,1820,1113,101.11,10.111,10,24300,2.73E-05,112000,2.784\r\n10.1016/S0925-8388(01)01804-7,1,-428,0.00549,Fe1.98Sn0.02O3,\"solid state reaction, air\",polycrystalline,300,,32.19,6569,1853,1117,303.23,10.108,30,10000,1.83E-05,183000,\r\n10.1016/S0925-8388(01)01804-7,0.467,-364,0.00853,Fe1.96Sn0.04O3,\"solid state reaction, air\",polycrystalline,300,6.84,32.44,13020,1860,1122,303.23,10.108,30,21400,2.84E-05,133000,2.289\r\n10.1016/S0925-8388(01)01804-7,0.492,-403,0.01,Fe1.98Ti0.02O3,\"solid state reaction, air\",polycrystalline,400,,31.91,13.87,1837,1111,101.11,10.111,10,20300,3.30E-05,162000,\r\n10.1016/S0925-8388(01)01804-7,0.214,-344,0.02,Fe1.96Ti0.04O3,\"solid state reaction, air\",polycrystalline,400,6.87,31.87,14.74,1829,1112,101.11,10.111,10,46700,5.53E-05,118000,6.641\r\n10.1016/S0925-8388(01)01804-7,0.206,-309,0.02,Fe1.94Ti0.06O3,\"solid state reaction, air\",polycrystalline,400,5.93,31.84,15.62,1820,1113,101.11,10.111,10,48600,4.63E-05,95300,7.994\r\n10.1016/S0925-8388(01)01804-7,0.515,-413,0.01,Fe1.98Sn0.02O3,\"solid state reaction, air\",polycrystalline,400,,32.19,6569,1853,1117,303.23,10.108,30,19400,3.32E-05,171000,\r\n10.1016/S0925-8388(01)01804-7,0.263,-336,0.02,Fe1.96Sn0.04O3,\"solid state reaction, air\",polycrystalline,400,6.17,32.44,13020,1860,1122,303.23,10.108,30,38000,4.27E-05,113000,6.005\r\n10.1016/S0925-8388(01)01804-7,0.18,-370,0.05,Fe1.98Ti0.02O3,\"solid state reaction, air\",polycrystalline,700,,31.91,13.87,1837,1111,101.11,10.111,10,55600,7.63E-05,137000,\r\n10.1016/S0925-8388(01)01804-7,0.094,-323,0.08,Fe1.96Ti0.04O3,\"solid state reaction, air\",polycrystalline,700,4.7,31.87,14.74,1829,1112,101.11,10.111,10,106000,0.000111,104000,38.6\r\n10.1016/S0925-8388(01)01804-7,0.076,-292,0.08,Fe1.94Ti0.06O3,\"solid state reaction, air\",polycrystalline,700,4.34,31.84,15.62,1820,1113,101.11,10.111,10,132000,0.000112,85300,51.9\r\n10.1016/S0925-8388(01)01804-7,0.213,-374,0.05,Fe1.98Sn0.02O3,\"solid state reaction, air\",polycrystalline,700,,32.19,6569,1853,1117,303.23,10.108,30,46900,6.56E-05,140000,\r\n10.1016/S0925-8388(01)01804-7,0.107,-318,0.07,Fe1.96Sn0.04O3,\"solid state reaction, air\",polycrystalline,700,4.22,32.44,13020,1860,1122,303.23,10.108,30,93000,9.40E-05,101000,37.7\r\n10.1016/S0925-8388(01)01804-7,0.138,-372,0.1,Fe1.98Ti0.02O3,\"solid state reaction, air\",polycrystalline,1000,,31.91,13.87,1837,1111,101.11,10.111,10,72400,0.0001,138000,\r\n10.1016/S0925-8388(01)01804-7,0.072,-328,0.15,Fe1.96Ti0.04O3,\"solid state reaction, air\",polycrystalline,1000,3.54,31.87,14.74,1829,1112,101.11,10.111,10,139000,0.00015,108000,95.6\r\n10.1016/S0925-8388(01)01804-7,0.058,-295,0.15,Fe1.94Ti0.06O3,\"solid state reaction, air\",polycrystalline,1000,3.35,31.84,15.62,1820,1113,101.11,10.111,10,174000,0.000151,86900,127\r\n10.1016/S0925-8388(01)01804-7,0.162,-375,0.09,Fe1.98Sn0.02O3,\"solid state reaction, air\",polycrystalline,1000,,32.19,6569,1853,1117,303.23,10.108,30,61600,8.64E-05,140000,\r\n10.1016/S0925-8388(01)01804-7,0.087,-323,0.12,Fe1.96Sn0.04O3,\"solid state reaction, air\",polycrystalline,1000,3.08,32.44,13020,1860,1122,303.23,10.108,30,115000,0.00012,105000,90.8\r\n10.1016/S0925-8388(02)00972-6,0.00701,-167,0.12,Sr0.95La0.05Ti1O3,\"solid state reaction, Ar\",polycrystalline,300,,37.21,2291,2640,1987,59.83,11.966,5,143,0.000398,27900,\r\n10.1016/S0925-8388(02)00972-6,0.00261,-98,0.11,Sr0.9La0.1Ti1O3,\"solid state reaction, Ar\",polycrystalline,300,5.88,37.72,3205,2856,2006,59.83,11.966,5,383,0.000364,9530,0.048\r\n10.1016/S0925-8388(02)00972-6,0.000613,-54,0.14,Sr0.8La0.2Ti1O3,\"solid state reaction, Ar\",polycrystalline,300,,38.75,4961,3271,2041,60,12,5,1630,0.00047,2880,\r\n10.1016/S0925-8388(02)00972-6,0.00443,-188,0.32,Sr0.95La0.05Ti1O3,\"solid state reaction, Ar\",polycrystalline,400,,37.21,2291,2640,1987,59.83,11.966,5,226,0.000798,35300,\r\n10.1016/S0925-8388(02)00972-6,0.00165,-115,0.32,Sr0.9La0.1Ti1O3,\"solid state reaction, Ar\",polycrystalline,400,5.28,37.72,3205,2856,2006,59.83,11.966,5,606,0.000801,13200,0.112\r\n10.1016/S0925-8388(02)00972-6,0.000534,-65,0.31,Sr0.8La0.2Ti1O3,\"solid state reaction, Ar\",polycrystalline,400,,38.75,4961,3271,2041,60,12,5,1870,0.000784,4190,\r\n10.1016/S0925-8388(02)00972-6,0.00918,-251,0.48,Sr0.95La0.05Ti1O3,\"solid state reaction, Ar\",polycrystalline,700,,37.21,2291,2640,1987,59.83,11.966,5,109,0.000687,63000,\r\n10.1016/S0925-8388(02)00972-6,0.00366,-179,0.61,Sr0.9La0.1Ti1O3,\"solid state reaction, Ar\",polycrystalline,700,3.83,37.72,3205,2856,2006,59.83,11.966,5,273,0.000876,32000,0.122\r\n10.1016/S0925-8388(02)00972-6,0.00119,-113,0.75,Sr0.8La0.2Ti1O3,\"solid state reaction, Ar\",polycrystalline,700,,38.75,4961,3271,2041,60,12,5,839,0.00107,12800,\r\n10.1016/S0925-8388(02)00972-6,0.018,-285,0.44,Sr0.95La0.05Ti1O3,\"solid state reaction, Ar\",polycrystalline,1000,,37.21,2291,2640,1987,59.83,11.966,5,54.6,0.000443,81200,\r\n10.1016/S0925-8388(02)00972-6,0.00793,-221,0.62,Sr0.9La0.1Ti1O3,\"solid state reaction, Ar\",polycrystalline,1000,3.15,37.72,3205,2856,2006,59.83,11.966,5,126,0.000616,48800,0.098\r\n10.1016/S0925-8388(02)00972-6,0.00238,-158,1.05,Sr0.8La0.2Ti1O3,\"solid state reaction, Ar\",polycrystalline,1000,,38.75,4961,3271,2041,60,12,5,420,0.00105,25000,\r\n10.1016/S0925-8388(02)01002-2,0.000711,4,0.000705,Mo3Te4,\"solid state reaction, vacuum\",polycrystalline,300,3.812,114.04,639700000,2718,5052,1039.77,24.756,42,1410,2.35E-06,16.7,0.27\r\n10.1016/S0925-8388(02)01002-2,0.000767,3,0.000439,Mo6Te7S1,\"solid state reaction, vacuum\",polycrystalline,300,2.773,107.22,595400000,2661,4975,1039.77,24.756,42,1300,1.46E-06,11.2,0.344\r\n10.1016/S0925-8388(02)01002-2,0.000857,6,0.00139,Mo6Te6S2,\"solid state reaction, vacuum\",polycrystalline,300,2.125,100.39,545100000,2596,4888,1039.77,24.756,42,1170,4.63E-06,39.7,0.402\r\n10.1016/S0925-8388(02)01002-2,0.00072,8,0.00313,Mo3Te4,\"solid state reaction, vacuum\",polycrystalline,400,3.912,114.04,639700000,2718,5052,1039.77,24.756,42,1390,7.83E-06,56.4,0.347\r\n10.1016/S0925-8388(02)01002-2,0.000783,5,0.00153,Mo6Te7S1,\"solid state reaction, vacuum\",polycrystalline,400,3.097,107.22,595400000,2661,4975,1039.77,24.756,42,1280,3.84E-06,30,0.402\r\n10.1016/S0925-8388(02)01002-2,0.000887,8,0.00293,Mo6Te6S2,\"solid state reaction, vacuum\",polycrystalline,400,2.374,100.39,545100000,2596,4888,1039.77,24.756,42,1130,7.33E-06,65,0.463\r\n10.1016/S0925-8388(02)01002-2,0.000715,17,0.03,Mo3Te4,\"solid state reaction, vacuum\",polycrystalline,700,4.452,114.04,639700000,2718,5052,1039.77,24.756,42,1400,3.84E-05,274,0.537\r\n10.1016/S0925-8388(02)01002-2,0.000817,14,0.02,Mo6Te7S1,\"solid state reaction, vacuum\",polycrystalline,700,3.978,107.22,595400000,2661,4975,1039.77,24.756,42,1220,2.39E-05,195,0.525\r\n10.1016/S0925-8388(02)01002-2,0.000946,12,0.01,Mo6Te6S2,\"solid state reaction, vacuum\",polycrystalline,700,2.931,100.39,545100000,2596,4888,1039.77,24.756,42,1060,1.44E-05,137,0.616\r\n10.1016/S0925-8388(02)01002-2,0.000723,24,0.08,Mo3Te4,\"solid state reaction, vacuum\",polycrystalline,1000,5.291,114.04,639700000,2718,5052,1039.77,24.756,42,1380,7.91E-05,572,0.638\r\n10.1016/S0925-8388(02)01002-2,0.000833,21,0.05,Mo6Te7S1,\"solid state reaction, vacuum\",polycrystalline,1000,4.61,107.22,595400000,2661,4975,1039.77,24.756,42,1200,5.35E-05,446,0.635\r\n10.1016/S0925-8388(02)01002-2,0.001,15,0.02,Mo6Te6S2,\"solid state reaction, vacuum\",polycrystalline,1000,3.454,100.39,545100000,2596,4888,1039.77,24.756,42,1000,2.14E-05,214,0.706\r\n10.1021/cm050412c,0.21,220,0.00691,Tl11.5Sb11.5Cu8Se27,\"solid state reaction, vacuum\",polycrystalline,300,,110.19,8301000,4990,3898,1468,25.31,58,4.762,2.30E-05,48400,\r\n10.1021/cm050412c,14500,-160,5.30E-08,Tl1Ti1P1S5,\"solid state reaction, vacuum\",polycrystalline,300,0.783,55.44,668700,3519,3878,374.96,23.435,16,6.90E-05,1.77E-10,25600,6.45E-08\r\n10.1021/cm050412c,130,345,2.75E-05,Tl2Cu2Sn1Te4,\"solid state reaction, vacuum\",polycrystalline,300,0.377,129.44,438700000,3984,4776,500.1,27.783,18,0.00769,9.16E-08,119000,1.49E-05\r\n10.1021/cm052055b,0.00598,-280,0.39,In0.05Co4Sb12,Solid state reaction,polycrystalline,300,2.087,106.08,4312000,7219,3308,739.646,23.042,32.1,167,0.00131,78300,0.059\r\n10.1021/cm052055b,0.00292,-257,0.68,In0.1Co4Sb12,Solid state reaction,polycrystalline,300,2.188,106.11,4314000,7205,3304,741.144,23.017,32.2,342,0.00227,66200,0.115\r\n10.1021/cm052055b,0.00187,-247,0.97,In0.15Co4Sb12,Solid state reaction,polycrystalline,300,2.299,106.13,4316000,7192,3300,741.39,22.953,32.3,534,0.00325,60800,0.17\r\n10.1021/cm052055b,0.00149,-222,0.99,In0.2Co4Sb12,Solid state reaction,polycrystalline,300,2.476,106.16,4318000,7180,3295,742.742,22.924,32.4,670,0.00331,49300,0.198\r\n10.1021/cm052055b,0.00114,-217,1.24,In0.25Co4Sb12,Solid state reaction,polycrystalline,300,2.559,106.19,4320000,7167,3291,742.89,22.858,32.5,878,0.00414,47100,0.251\r\n10.1021/cm052055b,0.00151,-212,0.89,In0.3Co4Sb12,Solid state reaction,polycrystalline,300,2.688,106.21,4322000,7154,3287,742.89,22.788,32.6,662,0.00297,44900,0.18\r\n10.1021/cm052055b,0.00677,-296,0.52,In0.05Co4Sb12,Solid state reaction,polycrystalline,400,1.738,106.08,4312000,7219,3308,739.646,23.042,32.1,148,0.00129,87400,0.083\r\n10.1021/cm052055b,0.0034,-276,0.9,In0.1Co4Sb12,Solid state reaction,polycrystalline,400,1.909,106.11,4314000,7205,3304,741.144,23.017,32.2,294,0.00224,76300,0.15\r\n10.1021/cm052055b,0.00213,-266,1.33,In0.15Co4Sb12,Solid state reaction,polycrystalline,400,1.995,106.13,4316000,7192,3300,741.39,22.953,32.3,470,0.00333,70900,0.23\r\n10.1021/cm052055b,0.00175,-248,1.41,In0.2Co4Sb12,Solid state reaction,polycrystalline,400,2.08,106.16,4318000,7180,3295,742.742,22.924,32.4,572,0.00352,61600,0.268\r\n10.1021/cm052055b,0.00134,-248,1.83,In0.25Co4Sb12,Solid state reaction,polycrystalline,400,2.265,106.19,4320000,7167,3291,742.89,22.858,32.5,746,0.00458,61500,0.321\r\n10.1021/cm052055b,0.00179,-247,1.36,In0.3Co4Sb12,Solid state reaction,polycrystalline,400,2.159,106.21,4322000,7154,3287,742.89,22.788,32.6,558,0.00341,61200,0.252\r\n10.1021/cm052055b,0.00843,-335,0.93,In0.05Co4Sb12,Solid state reaction,polycrystalline,700,1.564,106.08,4312000,7219,3308,739.646,23.042,32.1,119,0.00133,112000,0.129\r\n10.1021/cm052055b,0.00434,-310,1.55,In0.1Co4Sb12,Solid state reaction,polycrystalline,700,1.742,106.11,4314000,7205,3304,741.144,23.017,32.2,231,0.00221,96000,0.226\r\n10.1021/cm052055b,0.00269,-302,2.37,In0.15Co4Sb12,Solid state reaction,polycrystalline,700,1.862,106.13,4316000,7192,3300,741.39,22.953,32.3,372,0.00338,90900,0.341\r\n10.1021/cm052055b,0.00215,-282,2.59,In0.2Co4Sb12,Solid state reaction,polycrystalline,700,1.941,106.16,4318000,7180,3295,742.742,22.924,32.4,466,0.0037,79400,0.41\r\n10.1021/cm052055b,0.00166,-276,3.21,In0.25Co4Sb12,Solid state reaction,polycrystalline,700,2.135,106.19,4320000,7167,3291,742.89,22.858,32.5,604,0.00459,76000,0.483\r\n10.1021/cm052055b,0.00228,-278,2.38,In0.3Co4Sb12,Solid state reaction,polycrystalline,700,2.014,106.21,4322000,7154,3287,742.89,22.788,32.6,438,0.0034,77500,0.372\r\n10.1021/cm060261t,0.00204,56,0.05,Yb14Mn1Sb11,\"flux (Sn), Ar\",single crystal,300,0.84,146.81,1966000,8812,3211,6058.93,29.129,208,490,0.000156,3190,0.427\r\n10.1021/cm060261t,0.00232,69,0.08,Yb14Mn1Sb11,\"flux (Sn), Ar\",single crystal,400,0.844,146.81,1966000,8812,3211,6058.93,29.129,208,430,0.000203,4720,0.498\r\n10.1021/cm060261t,0.00346,117,0.28,Yb14Mn1Sb11,\"flux (Sn), Ar\",single crystal,700,0.816,146.81,1966000,8812,3211,6058.93,29.129,208,289,0.000397,13700,0.604\r\n10.1021/cm060261t,0.00458,164,0.59,Yb14Mn1Sb11,\"flux (Sn), Ar\",single crystal,1000,0.715,146.81,1966000,8812,3211,6058.93,29.129,208,218,0.000588,26900,0.745\r\n10.1021/cm200581k,0.045,279,0.05,Ag1Cr1Se2,\"solid state reaction, sealed\",polycrystalline,300,0.956,79.45,14290000,2031,2077,248.9,20.742,12,22.4,0.000175,78000,0.017\r\n10.1021/cm200581k,0.04,300,0.09,Ag1Cr1Se2,\"solid state reaction, sealed\",polycrystalline,400,0.4,79.45,14290000,2031,2077,248.9,20.742,12,24.9,0.000224,90100,0.061\r\n10.1021/cm200581k,0.033,307,0.2,Ag1Cr1Se2,\"solid state reaction, sealed\",polycrystalline,700,0.206,79.45,14290000,2031,2077,248.9,20.742,12,30.4,0.000286,94100,0.253\r\n10.1021/cm970397e,0.032,-196,0.04,K2Bi8Se13,Solid state reaction + extra,polycrystalline,300,1.285,120.72,42810000,4060,4518,1357.83,29.518,46,30.8,0.000119,38500,0.018\r\n10.1021/cm970397e,0.00416,-220,0.35,K2Bi8Se13,Flux (Bi self-flux),single crystal,300,,120.72,42810000,4060,4518,1357.83,29.518,46,240,0.00116,48200,\r\n10.1021/nl202439h,0.297,-210,0.00446,Zn0.9975Al0.0025O1,\"microwave solvothermal, air\",polycrystalline,300,2.78,40.64,10770,1363,1620,47.62,11.905,4,3.37,1.49E-05,44100,0.000887\r\n10.1021/nl202439h,0.195,-220,0.00995,Zn0.9975Al0.0025O1,\"microwave solvothermal, air\",polycrystalline,400,2.687,40.64,10770,1363,1620,47.62,11.905,4,5.14,2.49E-05,48400,0.00187\r\n10.1021/nl202439h,0.065,-268,0.08,Zn0.9975Al0.0025O1,\"microwave solvothermal, air\",polycrystalline,700,2.283,40.64,10770,1363,1620,47.62,11.905,4,15.3,0.00011,71800,0.011\r\n10.1021/nl202439h,0.012,-316,0.81,Zn0.9975Al0.0025O1,\"microwave solvothermal, air\",polycrystalline,1000,1.909,40.64,10770,1363,1620,47.62,11.905,4,81.5,0.000814,99900,0.104\r\n10.1021/nl8026795,0.00118,121,0.37,Si0.8Ge0.2,\"ball milling, hot-pressed nanopowders\",polycrystalline,300,2.449,37,270800,4928,1351,169.78,21.222,8,849,0.00124,14600,0.254\r\n10.1021/nl8026795,0.00129,138,0.59,Si0.8Ge0.2,\"ball milling, hot-pressed nanopowders\",polycrystalline,400,2.52,37,270800,4928,1351,169.78,21.222,8,774,0.00148,19200,0.3\r\n10.1021/nl8026795,0.00179,191,1.44,Si0.8Ge0.2,\"ball milling, hot-pressed nanopowders\",polycrystalline,700,2.566,37,270800,4928,1351,169.78,21.222,8,560,0.00205,36700,0.372\r\n10.1021/nl8026795,0.00248,232,2.16,Si0.8Ge0.2,\"ball milling, hot-pressed nanopowders\",polycrystalline,1000,2.555,37,270800,4928,1351,169.78,21.222,8,403,0.00216,53700,0.384\r\n10.1023/A:1018515223271,0.000434,-26,0.05,Ba1Pb1O3,Solid state reaction (under oxygen),polycrystalline,300,3.78,78.5,44820,2535,1822,311.43,15.572,20,2310,0.000156,676,0.446\r\n10.1023/A:1018515223271,0.000462,-24,0.04,Ba0.8Sr0.2Pb1O3,Solid state reaction (under oxygen),polycrystalline,300,2.746,76.52,45940,2579,1839,311.43,15.572,20,2160,0.000129,598,0.577\r\n10.1023/A:1018515223271,0.00131,-42,0.04,Ba0.6Sr0.4Pb1O3,Solid state reaction (under oxygen),polycrystalline,300,2.306,74.53,47120,2625,1856,301.96,15.098,20,766,0.000135,1760,0.243\r\n10.1023/A:1018515223271,0.00413,-83,0.05,Ba0.4Sr0.6Pb1O3,Solid state reaction (under oxygen),polycrystalline,300,2.295,72.54,48360,2674,1874,301.96,15.098,20,242,0.000166,6850,0.077\r\n10.1023/A:1018515223271,0.000509,-32,0.08,Ba1Pb1O3,Solid state reaction (under oxygen),polycrystalline,400,4.156,78.5,44820,2535,1822,311.43,15.572,20,1960,0.000201,1020,0.461\r\n10.1023/A:1018515223271,0.000476,-30,0.08,Ba0.8Sr0.2Pb1O3,Solid state reaction (under oxygen),polycrystalline,400,3.306,76.52,45940,2579,1839,311.43,15.572,20,2100,0.000193,917,0.62\r\n10.1023/A:1018515223271,0.00127,-51,0.08,Ba0.6Sr0.4Pb1O3,Solid state reaction (under oxygen),polycrystalline,400,2.364,74.53,47120,2625,1856,301.96,15.098,20,786,0.000207,2640,0.325\r\n10.1023/A:1018515223271,0.00395,-96,0.09,Ba0.4Sr0.6Pb1O3,Solid state reaction (under oxygen),polycrystalline,400,2.133,72.54,48360,2674,1874,301.96,15.098,20,253,0.000235,9300,0.116\r\n10.1023/A:1018515223271,0.000527,-34,0.15,Ba1Pb1O3,Solid state reaction (under oxygen),polycrystalline,700,5.116,78.5,44820,2535,1822,311.43,15.572,20,1900,0.000215,1130,0.634\r\n10.1023/A:1018515223271,0.000551,-42,0.22,Ba0.8Sr0.2Pb1O3,Solid state reaction (under oxygen),polycrystalline,700,4.029,76.52,45940,2579,1839,311.43,15.572,20,1820,0.000317,1740,0.77\r\n10.1023/A:1018515223271,0.00117,-66,0.26,Ba0.6Sr0.4Pb1O3,Solid state reaction (under oxygen),polycrystalline,700,2.445,74.53,47120,2625,1856,301.96,15.098,20,851,0.000368,4330,0.595\r\n10.1023/A:1018515223271,0.00351,-118,0.28,Ba0.4Sr0.6Pb1O3,Solid state reaction (under oxygen),polycrystalline,700,1.983,72.54,48360,2674,1874,301.96,15.098,20,285,0.000396,13900,0.245\r\n10.1023/A:1018515223271,0.000859,-30,0.11,Ba1Pb1O3,Solid state reaction (under oxygen),polycrystalline,1000,,78.5,44820,2535,1822,311.43,15.572,20,1160,0.000106,910,\r\n10.1023/A:1018515223271,0.000601,-34,0.19,Ba0.8Sr0.2Pb1O3,Solid state reaction (under oxygen),polycrystalline,1000,,76.52,45940,2579,1839,311.43,15.572,20,1660,0.000189,1140,\r\n10.1023/A:1018515223271,0.000687,-40,0.23,Ba0.6Sr0.4Pb1O3,Solid state reaction (under oxygen),polycrystalline,1000,,74.53,47120,2625,1856,79.51,15.902,5,1460,0.00023,1580,\r\n10.1023/A:1018515223271,0.000935,-52,0.29,Ba0.4Sr0.6Pb1O3,Solid state reaction (under oxygen),polycrystalline,1000,,72.54,48360,2674,1874,79.51,15.902,5,1070,0.000295,2750,\r\n10.1038/nature09996,0.000369,62,0.32,Na0.02Pb1Te1,melted,polycrystalline,300,3.996,165.97,380700000,2781,2979,269.84,33.73,8,2710,0.00106,3890,0.497\r\n10.1038/nature09996,0.000413,51,0.19,Na0.02Pb1Te0.85Se0.15,melted,polycrystalline,300,3.014,162.36,331500000,2754,2827,269.84,33.73,8,2420,0.000628,2600,0.588\r\n10.1038/nature09996,0.000512,59,0.2,Na0.02Pb1Te0.75Se0.25,melted,polycrystalline,300,2.696,159.95,297500000,2736,2721,269.84,33.73,8,1950,0.000675,3460,0.53\r\n10.1038/nature09996,0.000569,105,0.77,Na0.02Pb1Te1,melted,polycrystalline,400,2.675,165.97,380700000,2781,2979,269.84,33.73,8,1760,0.00194,11000,0.641\r\n10.1038/nature09996,0.000619,98,0.62,Na0.02Pb1Te0.85Se0.15,melted,polycrystalline,400,2.218,162.36,331500000,2754,2827,269.84,33.73,8,1620,0.00156,9670,0.711\r\n10.1038/nature09996,0.000691,90,0.47,Na0.02Pb1Te0.75Se0.25,melted,polycrystalline,400,2.154,159.95,297500000,2736,2721,269.84,33.73,8,1450,0.00117,8060,0.656\r\n10.1038/nature09996,0.00171,213,1.85,Na0.02Pb1Te1,melted,polycrystalline,700,1.393,165.97,380700000,2781,2979,269.84,33.73,8,584,0.00265,45300,0.716\r\n10.1038/nature09996,0.00161,209,1.91,Na0.02Pb1Te0.85Se0.15,melted,polycrystalline,700,1.268,162.36,331500000,2754,2827,269.84,33.73,8,623,0.00272,43700,0.839\r\n10.1038/nature09996,0.00163,205,1.81,Na0.02Pb1Te0.75Se0.25,melted,polycrystalline,700,1.296,159.95,297500000,2736,2721,269.84,33.73,8,612,0.00258,42100,0.807\r\n10.1038/nature09996,0.00205,204,2.03,Na0.02Pb1Te0.85Se0.15,melted,polycrystalline,1000,1.189,162.36,331500000,2754,2827,269.84,33.73,8,487,0.00203,41600,0.999\r\n10.1038/nature09996,0.00198,197,1.96,Na0.02Pb1Te0.75Se0.25,melted,polycrystalline,1000,1.196,159.95,297500000,2736,2721,269.84,33.73,8,504,0.00196,38800,1.029\r\n10.1038/nature11439,0.000679,81,0.29,Pb0.96Sr0.4Te1Na0.2,sparks plasma sintering,polycrystalline,300,2.85,143.03,348500000,2897,2980,269.84,33.73,8,1470,0.000966,6560,0.378\r\n10.1038/nature11439,0.00041,68,0.34,Pb0.98Sr0.2Te1Na0.1,melting,polycrystalline,300,3.065,153.72,364100000,2843,2981,269.84,33.73,8,2440,0.00113,4620,0.583\r\n10.1038/nature11439,0.000417,64,0.29,Pb0.98Te1Na0.2,melting,polycrystalline,300,4.29,153.79,380700000,2761,2963,269.84,33.73,8,2400,0.000983,4100,0.409\r\n10.1038/nature11439,0.000845,128,0.78,Pb0.96Sr0.4Te1Na0.2,sparks plasma sintering,polycrystalline,400,2.126,143.03,348500000,2897,2980,269.84,33.73,8,1180,0.00194,16400,0.544\r\n10.1038/nature11439,0.000707,117,0.77,Pb0.98Sr0.2Te1Na0.1,melting,polycrystalline,400,2.23,153.72,364100000,2843,2981,269.84,33.73,8,1420,0.00194,13700,0.619\r\n10.1038/nature11439,0.000576,105,0.77,Pb0.98Te1Na0.2,melting,polycrystalline,400,3.18,153.79,380700000,2761,2963,269.84,33.73,8,1740,0.00191,11000,0.533\r\n10.1038/nature11439,0.00212,239,1.88,Pb0.96Sr0.4Te1Na0.2,sparks plasma sintering,polycrystalline,700,1.18,143.03,348500000,2897,2980,269.84,33.73,8,471,0.00269,57100,0.682\r\n10.1038/nature11439,0.00301,263,1.61,Pb0.98Sr0.2Te1Na0.1,melting,polycrystalline,700,1.03,153.72,364100000,2843,2981,269.84,33.73,8,332,0.0023,69200,0.551\r\n10.1038/nature11439,0.00225,236,1.73,Pb0.98Te1Na0.2,melting,polycrystalline,700,1.44,153.79,380700000,2761,2963,269.84,33.73,8,444,0.00247,55700,0.527\r\n10.1038/nature11439,0.00315,265,2.23,Pb0.96Sr0.4Te1Na0.2,sparks plasma sintering,polycrystalline,1000,0.98,143.03,348500000,2897,2980,269.84,33.73,8,317,0.00223,70200,0.789\r\n10.1038/nmat3273,0.001,90,0.24,Cu2Se1,\"melted, vacuum\",polycrystalline,300,0.97,68.68,7674000,1825,1672,184.61,15.384,12,1000,0.00081,8100,0.755\r\n10.1038/nmat3274,0.00161,107,0.28,Cu2Se1,\"melted, vacuum\",polycrystalline,400,1.04,68.68,7674000,1825,1672,184.61,15.384,12,621,0.000711,11400,0.583\r\n10.1038/nmat3275,0.0042,201,0.67,Cu2Se1,\"melted, vacuum\",polycrystalline,700,0.915,68.68,7674000,1825,1672,184.61,15.384,12,238,0.000962,40400,0.444\r\n10.1038/nmat3276,0.0078,297,1.13,Cu2Se1,\"melted, vacuum\",polycrystalline,1000,0.745,68.68,7674000,1825,1672,184.61,15.384,12,128,0.00113,88200,0.42\r\n10.1038/nmat3277,0.000605,62,0.19,Cu1.98Se1,\"melted, vacuum\",polycrystalline,300,1.25,68.72,7721000,1826,1673,184.61,15.384,12,1650,0.000644,3890,0.968\r\n10.1038/nmat3278,0.000719,64,0.23,Cu1.98Se1,\"melted, vacuum\",polycrystalline,400,1.73,68.72,7721000,1826,1673,184.61,15.384,12,1390,0.000573,4120,0.785\r\n10.1038/nmat3279,0.00151,129,0.77,Cu1.98Se1,\"melted, vacuum\",polycrystalline,700,1.45,68.72,7721000,1826,1673,184.61,15.384,12,662,0.0011,16600,0.78\r\n10.1038/nmat3280,0.00325,202,1.25,Cu1.98Se1,\"melted, vacuum\",polycrystalline,1000,1.015,68.72,7721000,1826,1673,184.61,15.384,12,308,0.00125,40600,0.74\r\n10.1039/A602506D,0.26,-301,0.01,Zn1O1,\"solid state reaction, air\",polycrystalline,300,48.7,40.69,10780,1363,1621,47.62,11.905,4,0.059,3.49E-05,90600,8.89E-07\r\n10.1039/A602506D,0.00562,-154,0.13,Zn0.995Al0.005O1,\"solid state reaction, air\",polycrystalline,300,44.495,40.59,10760,1362,1619,47.62,11.905,4,155,0.000422,23700,0.00254\r\n10.1039/A602506D,0.00275,-179,0.35,Zn0.99Al0.01O1,\"solid state reaction, air\",polycrystalline,300,44.495,40.5,10730,1362,1616,47.62,11.905,4,312,0.00116,32000,0.00513\r\n10.1039/A602506D,0.0012,-138,0.47,Zn0.98Al0.02O1,\"solid state reaction, air\",polycrystalline,300,40.29,40.31,10670,1361,1612,47.62,11.905,4,779,0.00158,19000,0.014\r\n10.1039/A602506D,0.00132,-175,0.7,Zn0.95Al0.05O1,\"solid state reaction, air\",polycrystalline,300,34.5,39.73,10490,1358,1599,47.62,11.905,4,690,0.00232,30600,0.015\r\n10.1039/A602506D,0.389,-294,0.00888,Zn1O1,\"solid state reaction, air\",polycrystalline,400,33.22,40.69,10780,1363,1621,47.62,11.905,4,0.25,2.22E-05,86400,7.33E-06\r\n10.1039/A602506D,0.00617,-191,0.24,Zn0.995Al0.005O1,\"solid state reaction, air\",polycrystalline,400,30.21,40.59,10760,1362,1619,47.62,11.905,4,149,0.000589,36300,0.0048\r\n10.1039/A602506D,0.00339,-204,0.49,Zn0.99Al0.01O1,\"solid state reaction, air\",polycrystalline,400,30.21,40.5,10730,1362,1616,47.62,11.905,4,254,0.00123,41600,0.00819\r\n10.1039/A602506D,0.00129,-148,0.68,Zn0.98Al0.02O1,\"solid state reaction, air\",polycrystalline,400,27.2,40.31,10670,1361,1612,47.62,11.905,4,704,0.00169,21800,0.025\r\n10.1039/A602506D,0.00155,-174,0.78,Zn0.95Al0.05O1,\"solid state reaction, air\",polycrystalline,400,20.25,39.73,10490,1358,1599,47.62,11.905,4,569,0.00195,30200,0.027\r\n10.1039/A602506D,1.786,-330,0.00426,Zn1O1,\"solid state reaction, air\",polycrystalline,700,14.65,40.69,10780,1363,1621,47.62,11.905,4,9.345,6.09E-06,109000,0.00109\r\n10.1039/A602506D,0.00912,-166,0.21,Zn0.995Al0.005O1,\"solid state reaction, air\",polycrystalline,700,13.525,40.59,10760,1362,1619,47.62,11.905,4,94.9,0.000303,27600,0.012\r\n10.1039/A602506D,0.00398,-182,0.58,Zn0.99Al0.01O1,\"solid state reaction, air\",polycrystalline,700,13.525,40.5,10730,1362,1616,47.62,11.905,4,200,0.000834,33200,0.025\r\n10.1039/A602506D,0.00148,-171,1.39,Zn0.98Al0.02O1,\"solid state reaction, air\",polycrystalline,700,12.4,40.31,10670,1361,1612,47.62,11.905,4,548,0.00199,29400,0.075\r\n10.1039/A602506D,0.00209,-196,1.28,Zn0.95Al0.05O1,\"solid state reaction, air\",polycrystalline,700,14.3,39.73,10490,1358,1599,47.62,11.905,4,450,0.00183,38300,0.054\r\n10.1039/A602506D,2.97,-437,0.00643,Zn1O1,\"solid state reaction, air\",polycrystalline,1000,8.58,40.69,10780,1363,1621,47.62,11.905,4,21,6.43E-06,191000,0.00598\r\n10.1039/A602506D,0.00871,-232,0.62,Zn0.995Al0.005O1,\"solid state reaction, air\",polycrystalline,1000,8.25,40.59,10760,1362,1619,47.62,11.905,4,99.6,0.000616,53600,0.029\r\n10.1039/A602506D,0.00457,-167,0.61,Zn0.99Al0.01O1,\"solid state reaction, air\",polycrystalline,1000,8.25,40.5,10730,1362,1616,47.62,11.905,4,186,0.000611,27900,0.055\r\n10.1039/A602506D,0.00182,-175,1.68,Zn0.98Al0.02O1,\"solid state reaction, air\",polycrystalline,1000,7.92,40.31,10670,1361,1612,47.62,11.905,4,444,0.00168,30600,0.137\r\n10.1039/A602506D,0.00282,-200,1.42,Zn0.95Al0.05O1,\"solid state reaction, air\",polycrystalline,1000,6.23,39.73,10490,1358,1599,47.62,11.905,4,332,0.00142,40000,0.13\r\n10.1039/c0ee00517g,1.199,165,0.000681,Ca3Al1Sb3,\"solid state reaction, Ar\",polycrystalline,300,1.45,73.21,3564000,6623,2841,822.88,29.389,28,0.834,2.27E-06,27200,0.000421\r\n10.1039/c0ee00517g,0.098,90,0.00248,Ca2.97Na0.03Al1Sb3,\"solid state reaction, Ar\",polycrystalline,300,1.67,73.14,3567000,6622,2841,822.88,29.389,28,10.2,8.26E-06,8100,0.00447\r\n10.1039/c0ee00517g,0.059,82,0.00338,Ca2.94Na0.06Al1Sb3,\"solid state reaction, Ar\",polycrystalline,300,1.65,73.07,3571000,6621,2841,822.88,29.389,28,17,1.13E-05,6640,0.00753\r\n10.1039/c0ee00517g,0.028,113,0.01,Ca2.85Na0.15Al1Sb3,\"solid state reaction, Ar\",polycrystalline,300,1.59,72.85,3582000,6618,2841,822.88,29.389,28,36.4,4.61E-05,12700,0.017\r\n10.1039/c0ee00517g,0.538,316,0.00743,Ca3Al1Sb3,\"solid state reaction, Ar\",polycrystalline,400,1.1,73.21,3564000,6623,2841,822.88,29.389,28,1.86,1.86E-05,99800,0.00165\r\n10.1039/c0ee00517g,0.046,165,0.02,Ca2.97Na0.03Al1Sb3,\"solid state reaction, Ar\",polycrystalline,400,1.24,73.14,3567000,6622,2841,822.88,29.389,28,21.7,5.89E-05,27200,0.017\r\n10.1039/c0ee00517g,0.034,150,0.03,Ca2.94Na0.06Al1Sb3,\"solid state reaction, Ar\",polycrystalline,400,1.27,73.07,3571000,6621,2841,822.88,29.389,28,29.7,6.68E-05,22500,0.023\r\n10.1039/c0ee00517g,0.019,152,0.05,Ca2.85Na0.15Al1Sb3,\"solid state reaction, Ar\",polycrystalline,400,1.24,72.85,3582000,6618,2841,822.88,29.389,28,53.5,0.000124,23100,0.042\r\n10.1039/c0ee00517g,0.249,412,0.05,Ca3Al1Sb3,\"solid state reaction, Ar\",polycrystalline,700,0.745,73.21,3564000,6623,2841,822.88,29.389,28,4.023,6.82E-05,170000,0.00922\r\n10.1039/c0ee00517g,0.017,248,0.25,Ca2.97Na0.03Al1Sb3,\"solid state reaction, Ar\",polycrystalline,700,0.84,73.14,3567000,6622,2841,822.88,29.389,28,58.1,0.000358,61500,0.118\r\n10.1039/c0ee00517g,0.014,233,0.28,Ca2.94Na0.06Al1Sb3,\"solid state reaction, Ar\",polycrystalline,700,0.86,73.07,3571000,6621,2841,822.88,29.389,28,72.5,0.000393,54300,0.144\r\n10.1039/c0ee00517g,0.012,215,0.27,Ca2.85Na0.15Al1Sb3,\"solid state reaction, Ar\",polycrystalline,700,0.84,72.85,3582000,6618,2841,822.88,29.389,28,82,0.000379,46200,0.167\r\n10.1039/c0ee00517g,0.113,265,0.06,Ca3Al1Sb3,\"solid state reaction, Ar\",polycrystalline,1000,0.692,73.21,3564000,6623,2841,822.88,29.389,28,8.873,6.25E-05,70400,0.031\r\n10.1039/c0ee00517g,0.017,288,0.48,Ca2.97Na0.03Al1Sb3,\"solid state reaction, Ar\",polycrystalline,1000,0.67,73.14,3567000,6622,2841,822.88,29.389,28,58.1,0.000481,82700,0.212\r\n10.1039/c0ee00517g,0.013,262,0.51,Ca2.94Na0.06Al1Sb3,\"solid state reaction, Ar\",polycrystalline,1000,0.698,73.07,3571000,6621,2841,822.88,29.389,28,74.6,0.000512,68600,0.261\r\n10.1039/c0ee00517g,0.012,243,0.47,Ca2.85Na0.15Al1Sb3,\"solid state reaction, Ar\",polycrystalline,1000,0.68,72.85,3582000,6618,2841,822.88,29.389,28,80,0.000472,59000,0.287\r\n10.1039/c0jm02011g,0.00231,122,0.19,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,300,0.77,89.54,2919000,5264,2783,1610.64,25.566,63,433,0.000646,14900,0.412\r\n10.1039/c0jm02011g,0.00213,127,0.23,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,300,0.76,89.54,2919000,5264,2783,1610.64,25.566,63,470,0.000757,16100,0.453\r\n10.1039/c0jm02011g,0.00217,136,0.25,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,300,0.783,89.54,2919000,5264,2783,1610.64,25.566,63,460,0.00085,18500,0.43\r\n10.1039/c0jm02011g,0.00267,148,0.33,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,400,0.74,89.54,2919000,5264,2783,1610.64,25.566,63,375,0.000824,22000,0.494\r\n10.1039/c0jm02011g,0.00247,155,0.39,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,400,0.743,89.54,2919000,5264,2783,1610.64,25.566,63,405,0.000975,24100,0.533\r\n10.1039/c0jm02011g,0.00251,161,0.41,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,400,0.75,89.54,2919000,5264,2783,1610.64,25.566,63,399,0.00103,25900,0.519\r\n10.1039/c0jm02011g,0.00335,185,0.71,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,700,0.74,89.54,2919000,5264,2783,1610.64,25.566,63,298,0.00102,34100,0.688\r\n10.1039/c0jm02011g,0.00317,188,0.78,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,700,0.743,89.54,2919000,5264,2783,1610.64,25.566,63,316,0.00112,35500,0.726\r\n10.1039/c0jm02011g,0.00329,192,0.78,Zn4Sb3,\"solid state reaction, Ar\",polycrystalline,700,0.75,89.54,2919000,5264,2783,1610.64,25.566,63,304,0.00112,36800,0.692\r\n10.1039/C1JM10827A,0.00145,-151,0.47,Mg2Si0.999Bi0.001,\"mechanochemical, Ar\",polycrystalline,300,8.52,25.63,159900,5058,697.4,258.55,21.546,12,692,0.00158,22800,0.059\r\n10.1039/C1JM10827A,0.00082,-107,0.42,Mg2Si0.9985Bi0.0015,\"mechanochemical, Ar\",polycrystalline,300,7.08,25.66,239600,5058,704.6,258.55,21.546,12,1220,0.0014,11400,0.126\r\n10.1039/C1JM10827A,0.000488,-77,0.36,Mg2Si0.997Bi0.003,\"mechanochemical, Ar\",polycrystalline,300,6.16,25.75,477500,5060,725.9,258.55,21.546,12,2050,0.0012,5870,0.244\r\n10.1039/C1JM10827A,0.000369,-68,0.37,Mg2Si0.995Bi0.005,\"mechanochemical, Ar\",polycrystalline,300,6.55,25.87,792100,5061,754,258.55,21.546,12,2710,0.00124,4580,0.303\r\n10.1039/C1JM10827A,0.00033,-61,0.34,Mg2Si0.994Bi0.006,\"mechanochemical, Ar\",polycrystalline,300,6.55,25.93,948300,5062,768,258.55,21.546,12,3030,0.00113,3720,0.339\r\n10.1039/C1JM10827A,0.00171,-164,0.63,Mg2Si0.999Bi0.001,\"mechanochemical, Ar\",polycrystalline,400,5.7,25.63,159900,5058,697.4,258.55,21.546,12,586,0.00158,27000,0.1\r\n10.1039/C1JM10827A,0.000902,-149,0.98,Mg2Si0.9985Bi0.0015,\"mechanochemical, Ar\",polycrystalline,400,5.07,25.66,239600,5058,704.6,258.55,21.546,12,1110,0.00246,22200,0.213\r\n10.1039/C1JM10827A,0.000541,-101,0.75,Mg2Si0.997Bi0.003,\"mechanochemical, Ar\",polycrystalline,400,4.76,25.75,477500,5060,725.9,258.55,21.546,12,1850,0.00189,10200,0.379\r\n10.1039/C1JM10827A,0.000396,-84,0.7,Mg2Si0.995Bi0.005,\"mechanochemical, Ar\",polycrystalline,400,5.41,25.87,792100,5061,754,258.55,21.546,12,2530,0.00176,6970,0.456\r\n10.1039/C1JM10827A,0.000348,-79,0.71,Mg2Si0.993Bi0.007,\"mechanochemical, Ar\",polycrystalline,400,5.68,25.99,1104000,5063,781.9,258.55,21.546,12,2870,0.00178,6180,0.494\r\n10.1039/C1JM10827A,0.00317,-231,1.18,Mg2Si0.999Bi0.001,\"mechanochemical, Ar\",polycrystalline,700,3.66,25.63,159900,5058,697.4,258.55,21.546,12,316,0.00168,53400,0.147\r\n10.1039/C1JM10827A,0.00158,-217,2.09,Mg2Si0.9985Bi0.0015,\"mechanochemical, Ar\",polycrystalline,700,3.29,25.66,239600,5058,704.6,258.55,21.546,12,635,0.00299,47100,0.33\r\n10.1039/C1JM10827A,0.000929,-153,1.76,Mg2Si0.997Bi0.003,\"mechanochemical, Ar\",polycrystalline,700,3.53,25.75,477500,5060,725.9,258.55,21.546,12,1080,0.00252,23400,0.521\r\n10.1039/C1JM10827A,0.000621,-121,1.66,Mg2Si0.995Bi0.005,\"mechanochemical, Ar\",polycrystalline,700,4.29,25.87,792100,5061,754,258.55,21.546,12,1610,0.00237,14700,0.641\r\n10.1039/C1JM10827A,0.000569,-125,1.92,Mg2Si0.993Bi0.007,\"mechanochemical, Ar\",polycrystalline,700,4.4,25.99,1104000,5063,781.9,258.55,21.546,12,1760,0.00275,15600,0.682\r\n10.1039/c2jm16297k,1890,-175,4.87E-07,Li1Mn2O4,Solid state reaction (oxalates),polycrystalline,300,,25.83,2694,1254,1425,555.64,9.922,56,0.00053,1.62E-09,30600,\r\n10.1039/c2jm16297k,85.3,-147,1.01E-05,Li1Mn2O4,Solid state reaction (oxalates),polycrystalline,400,,25.83,2694,1254,1425,555.64,9.922,56,0.012,2.53E-08,21600,\r\n10.1039/c2jm16297k,1.691,-101,0.00042,Li1Mn2O4,Solid state reaction (oxalates),polycrystalline,700,,25.83,2694,1254,1425,555.64,9.922,56,0.591,5.99E-07,10100,\r\n10.1039/c2jm16297k,0.36,-85,0.002,Li1Mn2O4,Solid state reaction (oxalates),polycrystalline,1000,,25.83,2694,1254,1425,555.64,9.922,56,2.781,2.00E-06,7190,\r\n10.1063/1.121747,0.013,-320,0.24,Sr0.145Ga0.302Ge0.553,solid state reaction,polycrystalline,300,0.81,73.93,390200,5146,2085,1233.18,25.691,48,77.5,0.000794,102000,0.07\r\n10.1063/1.121747,0.00262,-154,0.27,Sr0.147Ga0.298Ge0.555,solid state reaction,polycrystalline,300,1.216,73.97,391100,5143,2087,1233.18,25.691,48,382,0.000905,23700,0.23\r\n10.1063/1.121747,0.00194,-128,0.25,Sr0.146Ga0.285Ge0.569,solid state reaction,polycrystalline,300,1.06,74,399800,5141,2086,1233.18,25.691,48,515,0.000845,16400,0.356\r\n10.1063/1.124182,0.0042,219,0.34,Tl2Sn1Te5,melted,polycrystalline,300,5.09,145.68,548000000,4127,5148,1045.95,32.686,32,238,0.00114,48000,0.034\r\n10.1063/1.124182,0.023,285,0.11,Tl2Ge1Te5,melted,polycrystalline,300,9.07,139.93,570500000,4364,5309,2027.01,31.672,64,43.2,0.000351,81200,0.00349\r\n10.1063/1.124182,0.00433,163,0.18,Tl2Sn1Te5,\"melted, hotpressed\",polycrystalline,300,6.75,145.68,548000000,4127,5148,1045.95,32.686,32,231,0.000614,26600,0.025\r\n10.1063/1.124182,0.00321,145,0.2,Tl2Sn1Te5,flux (TlTe2),single crystal,300,,145.68,548000000,4127,5148,1045.95,32.686,32,312,0.000655,21000,\r\n10.1063/1.1480115,0.011,117,0.04,Ca3Co4O9,\"solid state reaction, air\",polycrystalline,300,2,31.25,17150,2511,1757,147.11,10.865,13.54,93.7,0.000128,13700,0.034\r\n10.1063/1.1480115,0.00813,117,0.05,Ca2.7Na0.3Co4O9,\"solid state reaction, air\",polycrystalline,300,2,30.93,17330,2459,1745,147.11,10.865,13.54,123,0.000168,13700,0.045\r\n10.1063/1.1480115,0.01,135,0.05,Ca2.7Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,300,2,34.41,6713000,2799,2245,147.11,10.865,13.54,96.6,0.000177,18300,0.035\r\n10.1063/1.1480115,0.00936,132,0.06,Ca2.4Na0.3Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,300,2,34.09,6776000,2754,2239,147.11,10.865,13.54,107,0.000186,17400,0.039\r\n10.1063/1.1480115,0.011,121,0.05,Ca3Co4O9,\"solid state reaction, air\",polycrystalline,400,1.9,31.25,17150,2511,1757,147.11,10.865,13.54,89.1,0.00013,14600,0.046\r\n10.1063/1.1480115,0.00529,126,0.12,Ca2.7Na0.3Co4O9,\"solid state reaction, air\",polycrystalline,400,1.9,30.93,17330,2459,1745,147.11,10.865,13.54,189,0.000298,15800,0.097\r\n10.1063/1.1480115,0.01,141,0.08,Ca2.7Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,400,1.9,34.41,6713000,2799,2245,147.11,10.865,13.54,98.5,0.000195,19800,0.051\r\n10.1063/1.1480115,0.00922,145,0.09,Ca2.4Na0.3Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,400,1.9,34.09,6776000,2754,2239,147.11,10.865,13.54,108,0.000227,20900,0.056\r\n10.1063/1.1480115,0.0099,147,0.15,Ca3Co4O9,\"solid state reaction, air\",polycrystalline,700,1.8,31.25,17150,2511,1757,147.11,10.865,13.54,101,0.000218,21600,0.096\r\n10.1063/1.1480115,0.00801,154,0.21,Ca2.7Na0.3Co4O9,\"solid state reaction, air\",polycrystalline,700,2,30.93,17330,2459,1745,147.11,10.865,13.54,125,0.000295,23600,0.107\r\n10.1063/1.1480115,0.0091,169,0.22,Ca2.7Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,700,2,34.41,6713000,2799,2245,147.11,10.865,13.54,110,0.000314,28600,0.094\r\n10.1063/1.1480115,0.0085,173,0.25,Ca2.4Na0.3Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,700,1.8,34.09,6776000,2754,2239,147.11,10.865,13.54,118,0.000352,29900,0.112\r\n10.1063/1.1480115,0.00897,177,0.35,Ca3Co4O9,\"solid state reaction, air\",polycrystalline,1000,1.75,31.25,17150,2511,1757,147.11,10.865,13.54,112,0.000349,31300,0.155\r\n10.1063/1.1480115,0.00728,184,0.46,Ca2.7Na0.3Co4O9,\"solid state reaction, air\",polycrystalline,1000,2.05,30.93,17330,2459,1745,147.11,10.865,13.54,137,0.000465,33900,0.163\r\n10.1063/1.1480115,0.00783,197,0.49,Ca2.7Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,1000,2.05,34.41,6713000,2799,2245,147.11,10.865,13.54,128,0.000495,38700,0.152\r\n10.1063/1.1480115,0.00762,205,0.55,Ca2.4Na0.3Bi0.3Co4O9,\"solid state reaction, air\",polycrystalline,1000,1.75,34.09,6776000,2754,2239,147.11,10.865,13.54,131,0.000551,42000,0.183\r\n10.1063/1.1502190,0.00212,109,0.17,Bi2Sr2Co2O8,Solid state reaction + extra,single crystal,300,2.185,59.93,29310000,4016,4061,380.53,13.59,28,471,0.000558,11900,0.158\r\n10.1063/1.1502190,0.00238,120,0.24,Bi2Sr2Co2O8,Solid state reaction + extra,single crystal,400,2.125,59.93,29310000,4016,4061,380.53,13.59,28,420,0.000605,14400,0.193\r\n10.1063/1.1502190,0.00277,171,0.74,Bi2Sr2Co2O8,Solid state reaction + extra,single crystal,700,2.068,59.93,29310000,4016,4061,380.53,13.59,28,362,0.00106,29400,0.299\r\n10.1063/1.1502190,0.00367,294,2.35,Bi2Sr2Co2O8,Solid state reaction + extra,single crystal,1000,1.973,59.93,29310000,4016,4061,380.53,13.59,28,273,0.00235,86200,0.337\r\n10.1063/1.1687532,0.513,33,6.20E-05,Ca1Mn6.5Cu0.5O12,\"solid state reaction, air\",polycrystalline,300,,31.05,1387,1401,1359,598.91,9.982,60,1.949,2.07E-07,1060,\r\n10.1063/1.1687532,0.248,-13,2.09E-05,Ca1Mn6Cu1O12,\"solid state reaction, air\",polycrystalline,300,,31.26,2126,1401,1348,598.91,9.982,60,4.038,6.97E-08,173,\r\n10.1063/1.1687532,1720,-56,5.40E-08,Li1Mn2O4,\"solid state reaction, air\",polycrystalline,300,,25.83,2694,1254,1425,555.64,9.922,56,0.000581,1.80E-10,3100,\r\n10.1063/1.1687532,0.055,-22,0.000269,Pr0.5Ca0.5Mn1O3,\"solid state reaction, air\",polycrystalline,300,,38.69,40990,4428,1928,221.92,11.096,20,18.1,8.97E-07,496,\r\n10.1063/1.1687532,0.173,9,2.00E-05,Ca1Mn6.5Cu0.5O12,\"solid state reaction, air\",polycrystalline,400,,31.05,1387,1401,1359,598.91,9.982,60,5.793,5.00E-08,86.3,\r\n10.1063/1.1687532,0.101,-20,0.000157,Ca1Mn6Cu1O12,\"solid state reaction, air\",polycrystalline,400,,31.26,2126,1401,1348,598.91,9.982,60,9.895,3.93E-07,397,\r\n10.1063/1.1687532,74.1,-46,1.14E-06,Li1Mn2O4,\"solid state reaction, air\",polycrystalline,400,,25.83,2694,1254,1425,555.64,9.922,56,0.013,2.85E-09,2120,\r\n10.1063/1.1687532,0.03,-23,0.000696,Pr0.5Ca0.5Mn1O3,\"solid state reaction, air\",polycrystalline,400,,38.69,40990,4428,1928,221.92,11.096,20,33.5,1.74E-06,518,\r\n10.1063/1.1687532,0.089,8,5.05E-05,Ca1Mn7O12,\"solid state reaction, air\",polycrystalline,700,,30.83,636.4,1400,1370,598.91,9.982,60,11.2,7.21E-08,64.4,\r\n10.1063/1.1687532,0.05,-15,0.000329,Ca1Mn6.5Cu0.5O12,\"solid state reaction, air\",polycrystalline,700,,31.05,1387,1401,1359,598.91,9.982,60,20,4.70E-07,235,\r\n10.1063/1.1687532,0.033,-27,0.0016,Ca1Mn6Cu1O12,\"solid state reaction, air\",polycrystalline,700,,31.26,2126,1401,1348,598.91,9.982,60,30.6,2.29E-06,747,\r\n10.1063/1.1687532,1.167,-30,5.46E-05,Li1Mn2O4,\"solid state reaction, air\",polycrystalline,700,,25.83,2694,1254,1425,555.64,9.922,56,0.857,7.80E-08,911,\r\n10.1063/1.1687532,0.016,-23,0.00239,Pr0.5Ca0.5Mn1O3,\"solid state reaction, air\",polycrystalline,700,,38.69,40990,4428,1928,221.92,11.096,20,62.1,3.41E-06,549,\r\n10.1063/1.1687532,0.041,-20,0.001,Ca1Mn7O12,\"solid state reaction, air\",polycrystalline,1000,,30.83,636.4,1400,1370,598.91,9.982,60,24.7,1.00E-06,407,\r\n10.1063/1.1687532,0.028,-24,0.00211,Ca1Mn6.5Cu0.5O12,\"solid state reaction, air\",polycrystalline,1000,,31.05,1387,1401,1359,598.91,9.982,60,35.5,2.11E-06,593,\r\n10.1063/1.1687532,0.02,-30,0.00447,Ca1Mn6Cu1O12,\"solid state reaction, air\",polycrystalline,1000,,31.26,2126,1401,1348,598.91,9.982,60,49,4.47E-06,912,\r\n10.1063/1.1687532,0.261,-19,0.000144,Li1Mn2O4,\"solid state reaction, air\",polycrystalline,1000,,25.83,2694,1254,1425,555.64,9.922,56,3.83,1.44E-07,377,\r\n10.1063/1.1687532,0.013,-24,0.00443,Pr0.5Ca0.5Mn1O3,\"solid state reaction, air\",polycrystalline,1000,,38.69,40990,4428,1928,221.92,11.096,20,78.5,4.43E-06,564,\r\n10.1063/1.1868063,0.00975,-179,0.1,Zr0.5Hf0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,4.087,104.09,262000,2643,2022,226.87,18.906,12,103,0.000328,32000,0.018\r\n10.1063/1.1868063,0.00904,-189,0.12,Zr0.4Hf0.4Ti0.2Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,3.814,98.29,258100,2524,1954,226.87,18.906,12,111,0.000394,35600,0.021\r\n10.1063/1.1868063,0.00861,-370,0.48,Zr0.35Hf0.35Ti0.3Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,3.17,95.39,256000,2459,1917,226.87,18.906,12,116,0.00159,137000,0.027\r\n10.1063/1.1868063,0.00476,-312,0.61,Zr0.25Hf0.25Ti0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,3.063,89.59,251300,2315,1836,226.87,18.906,12,210,0.00204,97100,0.05\r\n10.1063/1.1868063,0.00481,-252,0.4,Zr0.15Hf0.15Ti0.7Ni1Sn1,\"arc-melted, Ar\",polycrystalline,300,3.394,83.79,246000,2152,1744,226.87,18.906,12,208,0.00132,63600,0.045\r\n10.1063/1.1868063,0.00626,-209,0.28,Zr0.5Hf0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,400,3.53,104.09,262000,2643,2022,226.87,18.906,12,160,0.000695,43500,0.044\r\n10.1063/1.1868063,0.00511,-234,0.43,Zr0.4Hf0.4Ti0.2Ni1Sn1,\"arc-melted, Ar\",polycrystalline,400,3.345,98.29,258100,2524,1954,226.87,18.906,12,196,0.00107,54600,0.057\r\n10.1063/1.1868063,0.00555,-379,1.04,Zr0.35Hf0.35Ti0.3Ni1Sn1,\"arc-melted, Ar\",polycrystalline,400,2.837,95.39,256000,2459,1917,226.87,18.906,12,180,0.00259,144000,0.062\r\n10.1063/1.1868063,0.00338,-330,1.29,Zr0.25Hf0.25Ti0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,400,3.003,89.59,251300,2315,1836,226.87,18.906,12,296,0.00322,109000,0.096\r\n10.1063/1.1868063,0.00313,-265,0.9,Zr0.15Hf0.15Ti0.7Ni1Sn1,\"arc-melted, Ar\",polycrystalline,400,3.072,83.79,246000,2152,1744,226.87,18.906,12,319,0.00224,70100,0.101\r\n10.1063/1.1868063,0.00217,-236,1.8,Zr0.5Hf0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,3.274,104.09,262000,2643,2022,226.87,18.906,12,462,0.00257,55700,0.241\r\n10.1063/1.1868063,0.00177,-277,3.03,Zr0.4Hf0.4Ti0.2Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,3.196,98.29,258100,2524,1954,226.87,18.906,12,566,0.00433,76600,0.303\r\n10.1063/1.1868063,0.00228,-348,3.72,Zr0.35Hf0.35Ti0.3Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,2.942,95.39,256000,2459,1917,226.87,18.906,12,438,0.00531,121000,0.255\r\n10.1063/1.1868063,0.00163,-328,4.62,Zr0.25Hf0.25Ti0.5Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,3.254,89.59,251300,2315,1836,226.87,18.906,12,612,0.0066,108000,0.321\r\n10.1063/1.1868063,0.00148,-261,3.21,Zr0.15Hf0.15Ti0.7Ni1Sn1,\"arc-melted, Ar\",polycrystalline,700,3.157,83.79,246000,2152,1744,226.87,18.906,12,675,0.00458,67900,0.365\r\n10.1063/1.2009828,0.254,388,0.02,Ag9Tl1Te5,melted,polycrystalline,300,0.2,120.88,358900000,2408,3201,4758.66,27.349,174,3.931,5.92E-05,151000,0.014\r\n10.1063/1.2009828,0.083,327,0.05,Ag9Tl1Te5,melted,polycrystalline,400,0.21,120.88,358900000,2408,3201,4758.66,27.349,174,12,0.000129,107000,0.056\r\n10.1063/1.2009828,0.026,311,0.26,Ag9Tl1Te5,melted,polycrystalline,700,0.2,120.88,358900000,2408,3201,4758.66,27.349,174,37.9,0.000366,96700,0.323\r\n10.1063/1.2163979,0.000662,-50,0.11,Ba8Ga16Ge30,\"Czochralski method, argon\",single crystal,300,1.94,81.36,356000,4753,2008,1254.12,23.224,54,1510,0.000378,2500,0.57\r\n10.1063/1.2163979,0.000791,-75,0.28,Ba8Ga16Ge30,\"Czochralski method, argon\",single crystal,400,1.79,81.36,356000,4753,2008,1254.12,23.224,54,1260,0.000711,5620,0.689\r\n10.1063/1.2163979,0.00142,-150,1.11,Ba8Ga16Ge30,\"Czochralski method, argon\",single crystal,700,1.56,81.36,356000,4753,2008,1254.12,23.224,54,705,0.00159,22500,0.772\r\n10.1063/1.2163979,0.002,-200,2,Ba8Ga16Ge30,\"Czochralski method, argon\",single crystal,1000,1.43,81.36,356000,4753,2008,1254.12,23.224,54,501,0.002,40000,0.855\r\n10.1063/1.2362922,0.012,-90,0.03,Ca0.9Nd0.1Mn1O3,Solid state reaction,polycrystalline,400,2.413,30.69,2894,2525,1444,210.93,10.546,20,83.8,6.83E-05,8150,0.034\r\n10.1063/1.2362922,0.011,-90,0.03,Ca0.9Tb0.1Mn1O3,Solid state reaction,polycrystalline,400,1.587,30.98,96250,2591,1460,209.02,10.451,20,93,7.58E-05,8150,0.057\r\n10.1063/1.2362922,0.00698,-90,0.05,Ca0.9Ho0.1Mn1O3,Solid state reaction,polycrystalline,400,2.068,31.1,85220,2618,1467,208.44,10.422,20,143,0.000117,8150,0.068\r\n10.1063/1.2362922,0.00406,-90,0.08,Ca0.9Yb0.1Mn1O3,Solid state reaction,polycrystalline,400,1.639,31.26,37270,2653,1475,207.52,10.376,20,247,0.000201,8150,0.147\r\n10.1063/1.2362922,0.461,-600,0.03,Ca1Mn1O3,Solid state reaction,polycrystalline,400,2.973,28.6,398,1861,1276,206.97,10.348,20,2.169,7.81E-05,360000,0.000712\r\n10.1063/1.2362922,0.017,-124,0.06,Ca0.9Nd0.1Mn1O3,Solid state reaction,polycrystalline,700,2.416,30.69,2894,2525,1444,210.93,10.546,20,57.5,8.81E-05,15300,0.041\r\n10.1063/1.2362922,0.015,-124,0.07,Ca0.9Tb0.1Mn1O3,Solid state reaction,polycrystalline,700,1.756,30.98,96250,2591,1460,209.02,10.451,20,65.2,0.0001,15300,0.063\r\n10.1063/1.2362922,0.00981,-124,0.11,Ca0.9Ho0.1Mn1O3,Solid state reaction,polycrystalline,700,2.185,31.1,85220,2618,1467,208.44,10.422,20,102,0.000156,15300,0.08\r\n10.1063/1.2362922,0.00599,-124,0.18,Ca0.9Yb0.1Mn1O3,Solid state reaction,polycrystalline,700,1.609,31.26,37270,2653,1475,207.52,10.376,20,167,0.000256,15300,0.177\r\n10.1063/1.2362922,0.233,-375,0.04,Ca1Mn1O3,Solid state reaction,polycrystalline,700,2.165,28.6,398,1861,1276,206.97,10.348,20,4.29,6.03E-05,140000,0.00338\r\n10.1063/1.2362922,0.021,-130,0.08,Ca0.9Nd0.1Mn1O3,Solid state reaction,polycrystalline,1000,2.382,30.69,2894,2525,1444,210.93,10.546,20,46.9,7.93E-05,16900,0.048\r\n10.1063/1.2362922,0.018,-130,0.09,Ca0.9Tb0.1Mn1O3,Solid state reaction,polycrystalline,1000,1.842,30.98,96250,2591,1460,209.02,10.451,20,54.4,9.19E-05,16900,0.072\r\n10.1063/1.2362922,0.012,-130,0.14,Ca0.9Ho0.1Mn1O3,Solid state reaction,polycrystalline,1000,2.239,31.1,85220,2618,1467,208.44,10.422,20,80,0.000135,16900,0.087\r\n10.1063/1.2362922,0.00825,-130,0.2,Ca0.9Yb0.1Mn1O3,Solid state reaction,polycrystalline,1000,1.588,31.26,37270,2653,1475,207.52,10.376,20,121,0.000205,16900,0.186\r\n10.1063/1.2362922,0.083,-321,0.12,Ca1Mn1O3,Solid state reaction,polycrystalline,1000,2.092,28.6,398,1861,1276,206.97,10.348,20,12,0.000123,103000,0.014\r\n10.1063/1.2828713,0.00123,-119,0.35,Nb1Co1Sn1,Floating zone melting,single crystal,300,6.904,90.18,221500,4729,4317,210.86,17.572,12,814,0.00116,14200,0.086\r\n10.1063/1.2828713,0.00137,-163,0.58,Nb1Co1.05Sn1,Floating zone melting,single crystal,300,6.887,89.67,219500,4711,4299,210.86,17.572,12,728,0.00194,26700,0.077\r\n10.1063/1.2828713,0.00111,-131,0.46,Nb1Co1.10Sn1,Floating zone melting,single crystal,300,5.802,89.17,217500,4693,4281,210.86,17.572,12,901,0.00154,17100,0.114\r\n10.1063/1.2828713,0.00141,-137,0.53,Nb1Co1Sn1,Floating zone melting,single crystal,400,7.958,90.18,221500,4729,4317,210.86,17.572,12,707,0.00133,18800,0.087\r\n10.1063/1.2828713,0.00163,-185,0.84,Nb1Co1.05Sn1,Floating zone melting,single crystal,400,7.01,89.67,219500,4711,4299,210.86,17.572,12,613,0.00211,34400,0.085\r\n10.1063/1.2828713,0.0013,-152,0.71,Nb1Co1.10Sn1,Floating zone melting,single crystal,400,5.83,89.17,217500,4693,4281,210.86,17.572,12,771,0.00178,23100,0.129\r\n10.1063/1.2828713,0.00203,-168,0.97,Nb1Co1Sn1,Floating zone melting,single crystal,700,9.741,90.18,221500,4729,4317,210.86,17.572,12,493,0.00139,28200,0.086\r\n10.1063/1.2828713,0.00234,-237,1.68,Nb1Co1.05Sn1,Floating zone melting,single crystal,700,7.232,89.67,219500,4711,4299,210.86,17.572,12,428,0.0024,56100,0.101\r\n10.1063/1.2828713,0.00184,-189,1.36,Nb1Co1.10Sn1,Floating zone melting,single crystal,700,6.232,89.17,217500,4693,4281,210.86,17.572,12,543,0.00194,35800,0.149\r\n10.1063/1.2828713,0.00259,-178,1.22,Nb1Co1Sn1,Floating zone melting,single crystal,1000,9.927,90.18,221500,4729,4317,210.86,17.572,12,386,0.00122,31500,0.095\r\n10.1063/1.2828713,0.00298,-251,2.11,Nb1Co1.05Sn1,Floating zone melting,single crystal,1000,7.672,89.67,219500,4711,4299,210.86,17.572,12,336,0.00211,62900,0.107\r\n10.1063/1.2828713,0.00242,-199,1.64,Nb1Co1.10Sn1,Floating zone melting,single crystal,1000,6.773,89.17,217500,4693,4281,210.86,17.572,12,413,0.00164,39800,0.149\r\n10.1063/1.3117943,0.00476,-54,0.02,Sr2Ti0.8Nb0.2O4,\"solid state reaction, Ar\",polycrystalline,300,4.37,42.3,5035,3261,2636,187,13.357,14,210,6.03E-05,2870,0.035\r\n10.1063/1.3117943,0.00186,-42,0.03,Sr3Ti1.6Nb0.4O7,\"solid state reaction, Ar\",polycrystalline,300,4.96,40.72,5611,3187,2641,305,12.708,24,538,9.67E-05,1800,0.079\r\n10.1063/1.3117943,0.00145,-52,0.06,Sr1Ti0.8Nb0.2O3,\"solid state reaction, Ar\",polycrystalline,300,10.42,38.5,6498,3072,2648,240.63,12.032,20,689,0.000187,2720,0.048\r\n10.1063/1.3117943,0.00567,-68,0.03,Sr2Ti0.8Nb0.2O4,\"solid state reaction, Ar\",polycrystalline,400,3.59,42.3,5035,3261,2636,187,13.357,14,176,8.06E-05,4570,0.048\r\n10.1063/1.3117943,0.00217,-57,0.06,Sr3Ti1.6Nb0.4O7,\"solid state reaction, Ar\",polycrystalline,400,3.89,40.72,5611,3187,2641,305,12.708,24,460,0.00015,3270,0.115\r\n10.1063/1.3117943,0.00142,-62,0.11,Sr1Ti0.8Nb0.2O3,\"solid state reaction, Ar\",polycrystalline,400,8.62,38.5,6498,3072,2648,240.63,12.032,20,704,0.000274,3890,0.08\r\n10.1063/1.3117943,0.00865,-110,0.1,Sr2Ti0.8Nb0.2O4,\"solid state reaction, Ar\",polycrystalline,700,2.48,42.3,5035,3261,2636,187,13.357,14,116,0.000141,12200,0.08\r\n10.1063/1.3117943,0.00429,-98,0.16,Sr3Ti1.6Nb0.4O7,\"solid state reaction, Ar\",polycrystalline,700,2.72,40.72,5611,3187,2641,305,12.708,24,233,0.000225,9660,0.146\r\n10.1063/1.3117943,0.00171,-110,0.5,Sr1Ti0.8Nb0.2O3,\"solid state reaction, Ar\",polycrystalline,700,4.92,38.5,6498,3072,2648,240.63,12.032,20,585,0.000708,12100,0.203\r\n10.1063/1.3117943,0.013,-167,0.21,Sr2Ti0.8Nb0.2O4,\"solid state reaction, Ar\",polycrystalline,1000,1.92,42.3,5035,3261,2636,187,13.357,14,75,0.000209,27900,0.095\r\n10.1063/1.3117943,0.00781,-158,0.32,Sr3Ti1.6Nb0.4O7,\"solid state reaction, Ar\",polycrystalline,1000,2.14,40.72,5611,3187,2641,305,12.708,24,128,0.00032,25000,0.146\r\n10.1063/1.3117943,0.00256,-165,1.06,Sr1Ti0.8Nb0.2O3,\"solid state reaction, Ar\",polycrystalline,1000,3.14,38.5,6498,3072,2648,240.63,12.032,20,390,0.00106,27200,0.303\r\n10.1063/1.3291563,0.00283,-92,0.09,Sr0.61Ba0.39Nb2O6,\"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\",single crystal,300,1.667,43.2,26540,5182,5061,610.4,13.564,45,354,0.000302,8540,0.155\r\n10.1063/1.3291563,0.105,-186,0.00988,Sr0.61Ba0.39Nb2O6,\"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\",single crystal,300,1.667,43.2,26540,5182,5061,610.4,13.564,45,9.522,3.29E-05,34600,0.00418\r\n10.1063/1.3291563,0.015,-194,0.1,Sr0.61Ba0.39Nb2O6,\"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\",single crystal,400,2.02,43.2,26540,5182,5061,610.4,13.564,45,68.4,0.000258,37600,0.033\r\n10.1063/1.3291563,0.0014,-201,2.02,Sr0.61Ba0.39Nb2O6,\"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\",single crystal,700,2.172,43.2,26540,5182,5061,610.4,13.564,45,714,0.00289,40400,0.562\r\n10.1063/1.348408,0.00133,128,0.37,Si0.79936Ge0.19984B0.0008,Vacuum hot pressed,polycrystalline,300,4.34,36.98,270800,4927,1352,169.78,21.222,8,750,0.00122,16300,0.126\r\n10.1063/1.348408,0.00117,-123,0.39,Si0.7956Ge0.1989P0.0055,Vacuum hot pressed,polycrystalline,300,4.139,36.96,269600,4914,1369,169.78,21.222,8,855,0.00129,15100,0.151\r\n10.1063/1.348408,0.00152,151,0.6,Si0.79936Ge0.19984B0.0008,Vacuum hot pressed,polycrystalline,400,4.145,36.98,270800,4927,1352,169.78,21.222,8,659,0.00151,22900,0.155\r\n10.1063/1.348408,0.00134,-150,0.67,Si0.7956Ge0.1989P0.0055,Vacuum hot pressed,polycrystalline,400,4.229,36.96,269600,4914,1369,169.78,21.222,8,749,0.00169,22500,0.173\r\n10.1063/1.348408,0.00218,210,1.41,Si0.79936Ge0.19984B0.0008,Vacuum hot pressed,polycrystalline,700,3.817,36.98,270800,4927,1352,169.78,21.222,8,458,0.00202,44000,0.205\r\n10.1063/1.348408,0.00194,-231,1.92,Si0.7956Ge0.1989P0.0055,Vacuum hot pressed,polycrystalline,700,3.723,36.96,269600,4914,1369,169.78,21.222,8,515,0.00274,53300,0.236\r\n10.1063/1.348408,0.00295,248,2.09,Si0.79936Ge0.19984B0.0008,Vacuum hot pressed,polycrystalline,1000,3.599,36.98,270800,4927,1352,169.78,21.222,8,339,0.00209,61600,0.23\r\n10.1063/1.348408,0.0025,-281,3.16,Si0.7956Ge0.1989P0.0055,Vacuum hot pressed,polycrystalline,1000,3.666,36.96,269600,4914,1369,169.78,21.222,8,399,0.00316,79200,0.266\r\n10.1063/1.3682585,0.0033,-102,0.09,Ba8Au5.14Si39.51,\"melted, inert\",polyrystalline,300,1.86,61.17,78590000,2988,1472,1132.02,20.963,54,303,0.000315,10400,0.119\r\n10.1063/1.3682585,0.00234,106,0.14,Ba8Au5.59Si39.01,\"melted, inert\",polyrystalline,300,1.77,62.65,83530000,2930,1462,1132.02,20.963,54,427,0.000482,11300,0.177\r\n10.1063/1.3682585,0.000617,46,0.1,Ba8Au6.10Si38.97,\"melted, inert\",polyrystalline,300,2.18,63.97,88490000,2876,1450,1132.02,20.963,54,1620,0.000347,2140,0.544\r\n10.1063/1.3682585,0.00342,-118,0.16,Ba8Au5.14Si39.51,\"melted, inert\",polyrystalline,400,1.61,61.17,78590000,2988,1472,1132.02,20.963,54,292,0.000408,13900,0.177\r\n10.1063/1.3682585,0.00253,126,0.25,Ba8Au5.59Si39.01,\"melted, inert\",polyrystalline,400,1.62,62.65,83530000,2930,1462,1132.02,20.963,54,395,0.000632,16000,0.238\r\n10.1063/1.3682585,0.000702,57,0.19,Ba8Au6.10Si38.97,\"melted, inert\",polyrystalline,400,2.33,63.97,88490000,2876,1450,1132.02,20.963,54,1420,0.000463,3250,0.597\r\n10.1063/1.3682585,0.00287,-98,0.24,Ba8Au5.14Si39.51,\"melted, inert\",polyrystalline,700,2.45,61.17,78590000,2988,1472,1132.02,20.963,54,348,0.000336,9650,0.243\r\n10.1063/1.3682585,0.00275,136,0.47,Ba8Au5.59Si39.01,\"melted, inert\",polyrystalline,700,2.41,62.65,83530000,2930,1462,1132.02,20.963,54,364,0.000677,18600,0.258\r\n10.1063/1.3682585,0.000789,77,0.52,Ba8Au6.10Si38.97,\"melted, inert\",polyrystalline,700,2.95,63.97,88490000,2876,1450,1132.02,20.963,54,1270,0.000749,5910,0.734\r\n10.1063/1.4765358,0.0075,-200,0.16,Ti1Ni1Sn1,Magnetic levitation induction furnace,polycrystalline,300,7.72,75.09,236400,1861,1579,208.21,17.351,12,133,0.000533,40000,0.013\r\n10.1063/1.4765358,0.0051,-245,0.47,Ti1Ni1Sn1,Magnetic levitation induction furnace,polycrystalline,400,6.72,75.09,236400,1861,1579,208.21,17.351,12,196,0.00118,60000,0.028\r\n10.1063/1.4765358,0.00217,-233,1.75,Ti1Ni1Sn1,Magnetic levitation induction furnace,polycrystalline,700,5.51,75.09,236400,1861,1579,208.21,17.351,12,461,0.0025,54300,0.143\r\n10.1063/1.4765358,0.0015,-155,1.6,Ti1Ni1Sn1,Magnetic levitation induction furnace,polycrystalline,1000,7.71,75.09,236400,1861,1579,208.21,17.351,12,667,0.0016,24000,0.211\r\n10.1103/PhysRevB.59.192,0.073,218,0.02,La2Cu1O4,Solid state reaction,polycrystalline,300,,57.91,21230,6820,2462,338.06,12.074,28,13.8,6.52E-05,47300,\r\n10.1103/PhysRevB.60.14057,0.249,69,0.000581,Sm1.7Ca0.3Mn1O3,\"solid state reaction, air\",polycrystalline,300,1.1,61.76,105900,6963,2537,219.13,10.956,20,4.018,1.94E-06,4820,0.00267\r\n10.1103/PhysRevB.60.14057,0.00955,-33,0.00333,Sm0.5Ca0.5Mn1O3,\"solid state reaction, air\",polycrystalline,300,1.9,39.63,58430,4548,1956,219.13,10.956,20,105,1.11E-05,1060,0.04\r\n10.1103/PhysRevB.60.14057,0.029,-358,0.13,Ca1Mn1O3,\"solid state reaction, air\",polycrystalline,300,16.23,28.6,398,1861,1276,206.97,10.348,20,35,0.000448,128000,0.00158\r\n10.1103/PhysRevB.77.075203,0.00066,-43,0.08,Ba8Ga16Ge30,\"Czochralski method, He\",single crystal,300,1.7,81.36,356000,4753,2008,1254.12,23.224,54,1520,0.000277,1830,0.652\r\n10.1103/PhysRevB.77.075203,0.000782,-50,0.09,Ba8Ga16Ge30,\"solid state reaction, Ar\",polycrystalline,300,1.52,81.36,356000,4753,2008,1254.12,23.224,54,1280,0.000315,2470,0.616\r\n10.1103/PhysRevB.77.075203,0.00076,-56,0.16,Ba8Ga16Ge30,\"Czochralski method, He\",single crystal,400,1.63,81.36,356000,4753,2008,1254.12,23.224,54,1320,0.000412,3130,0.788\r\n10.1103/PhysRevB.77.075203,0.0009,-62,0.17,Ba8Ga16Ge30,\"solid state reaction, Ar\",polycrystalline,400,1.42,81.36,356000,4753,2008,1254.12,23.224,54,1110,0.000429,3860,0.764\r\n10.1103/PhysRevB.77.075203,0.00123,-102,0.6,Ba8Ga16Ge30,\"Czochralski method, He\",single crystal,700,1.62,81.36,356000,4753,2008,1254.12,23.224,54,813,0.00085,10500,0.857\r\n10.1103/PhysRevB.77.075203,0.00161,-107,0.5,Ba8Ga16Ge30,\"solid state reaction, Ar\",polycrystalline,700,1.3,81.36,356000,4753,2008,1254.12,23.224,54,621,0.000716,11500,0.816\r\n10.1103/PhysRevB.77.075203,0.00171,-142,1.18,Ba8Ga16Ge30,\"Czochralski method, He\",single crystal,1000,1.6,81.36,356000,4753,2008,1254.12,23.224,54,585,0.00118,20200,0.892\r\n10.1103/PhysRevB.77.075203,0.00223,-144,0.94,Ba8Ga16Ge30,\"solid state reaction, Ar\",polycrystalline,1000,1.26,81.36,356000,4753,2008,1254.12,23.224,54,448,0.000935,20900,0.868\r\n10.1103/PhysRevB.80.115103,0.587,295,0.00444,Cu1Rh1O2,\"solid state reaction , air\",polycrystalline,300,,49.61,518600000,2265,4717,140.56,11.713,12,1.704,1.48E-05,86900,\r\n10.1103/PhysRevB.80.115103,0.131,261,0.02,Cu1Rh0.99Mg0.01O2,\"solid state reaction , air\",polycrystalline,300,,49.42,515400000,2263,4695,140.56,11.713,12,7.61,5.18E-05,68100,\r\n10.1103/PhysRevB.80.115103,0.011,174,0.08,Cu1Rh0.96Mg0.04O2,\"solid state reaction , air\",polycrystalline,300,,48.83,505800000,2259,4627,140.56,11.713,12,90.9,0.000277,30400,\r\n10.1103/PhysRevB.80.115103,0.00164,100,0.18,Cu1Rh0.9Mg0.1O2,\"solid state reaction , air\",polycrystalline,300,,47.65,485900000,2250,4486,140.56,11.713,12,610,0.000606,9940,\r\n10.1103/PhysRevB.80.115103,0.219,275,0.01,Cu1Rh1O2,\"solid state reaction , air\",polycrystalline,400,,49.61,518600000,2265,4717,140.56,11.713,12,4.56,3.46E-05,75800,\r\n10.1103/PhysRevB.80.115103,0.066,259,0.04,Cu1Rh0.99Mg0.01O2,\"solid state reaction , air\",polycrystalline,400,,49.42,515400000,2263,4695,140.56,11.713,12,15.2,0.000102,67100,\r\n10.1103/PhysRevB.80.115103,0.011,188,0.13,Cu1Rh0.96Mg0.04O2,\"solid state reaction , air\",polycrystalline,400,,48.83,505800000,2259,4627,140.56,11.713,12,89.3,0.000315,35300,\r\n10.1103/PhysRevB.80.115103,0.00196,115,0.27,Cu1Rh0.9Mg0.1O2,\"solid state reaction , air\",polycrystalline,400,,47.65,485900000,2250,4486,140.56,11.713,12,510,0.000675,13200,\r\n10.1103/PhysRevB.80.115103,0.102,292,0.06,Cu1Rh1O2,\"solid state reaction , air\",polycrystalline,700,,49.61,518600000,2265,4717,140.56,11.713,12,9.775,8.36E-05,85500,\r\n10.1103/PhysRevB.80.115103,0.046,283,0.12,Cu1Rh0.99Mg0.01O2,\"solid state reaction , air\",polycrystalline,700,,49.42,515400000,2263,4695,140.56,11.713,12,21.8,0.000175,80100,\r\n10.1103/PhysRevB.80.115103,0.014,232,0.28,Cu1Rh0.96Mg0.04O2,\"solid state reaction , air\",polycrystalline,700,,48.83,505800000,2259,4627,140.56,11.713,12,73,0.000393,53800,\r\n10.1103/PhysRevB.80.115103,0.00299,145,0.49,Cu1Rh0.9Mg0.1O2,\"solid state reaction , air\",polycrystalline,700,,47.65,485900000,2250,4486,140.56,11.713,12,334,0.000702,21000,\r\n10.1103/PhysRevB.80.115103,0.107,317,0.09,Cu1Rh1O2,\"solid state reaction , air\",polycrystalline,1000,,49.61,518600000,2265,4717,140.56,11.713,12,9.381,9.43E-05,100000,\r\n10.1103/PhysRevB.80.115103,0.049,315,0.2,Cu1Rh0.99Mg0.01O2,\"solid state reaction , air\",polycrystalline,1000,,49.42,515400000,2263,4695,140.56,11.713,12,20.5,0.000203,99200,\r\n10.1103/PhysRevB.80.115103,0.017,271,0.43,Cu1Rh0.96Mg0.04O2,\"solid state reaction , air\",polycrystalline,1000,,48.83,505800000,2259,4627,140.56,11.713,12,58.5,0.000429,73400,\r\n10.1103/PhysRevB.80.115103,0.00408,168,0.69,Cu1Rh0.6Mg0.4O2,\"solid state reaction , air\",polycrystalline,1000,,41.75,369700000,2199,3662,140.56,11.713,12,245,0.000693,28300,\r\n10.1103/PhysRevB.81.125205,0.00053,-45,0.11,La3Te3.8Sb0.2,\"solid state reaction, Ar\",polycrystalline,300,2.402,132.28,523800000,5987,4082,893.06,31.895,28,1890,0.000382,2020,0.575\r\n10.1103/PhysRevB.81.125205,0.0011,-53,0.08,La3Te3.65Sb0.35,\"solid state reaction, Ar\",polycrystalline,300,2.05,132.15,503700000,6089,4051,893.06,31.895,28,909,0.000255,2810,0.325\r\n10.1103/PhysRevB.81.125205,0.018,-91,0.01,La3Te3.35Sb0.65,\"solid state reaction, Ar\",polycrystalline,300,1.47,131.9,463400000,6293,3990,893.06,31.895,28,55.6,4.60E-05,8280,0.028\r\n10.1103/PhysRevB.81.125205,0.0071,-71,0.02,La3Te3.35Bi0.65,\"solid state reaction, Ar\",polycrystalline,300,1.967,140,444300000,6025,4313,893.06,31.895,28,141,7.10E-05,5040,0.052\r\n10.1103/PhysRevB.81.125205,0.00061,-41,0.08,La2.99Te4,\"solid state reaction, Ar\",polycrystalline,300,2.46,132.44,551400000,5846,4124,893.06,31.895,28,1640,0.000274,1670,0.488\r\n10.1103/PhysRevB.81.125205,0.0027,-41,0.02,La2.74Te4,\"solid state reaction, Ar\",polycrystalline,300,1.24,132.2,572900000,5704,4163,893.06,31.895,28,370,6.23E-05,1680,0.219\r\n10.1103/PhysRevB.81.125205,0.000589,-47,0.15,La3Te3.8Sb0.2,\"solid state reaction, Ar\",polycrystalline,400,2.58,132.28,523800000,5987,4082,893.06,31.895,28,1700,0.000369,2170,0.642\r\n10.1103/PhysRevB.81.125205,0.00137,-58,0.1,La3Te3.65Sb0.35,\"solid state reaction, Ar\",polycrystalline,400,2.06,132.15,503700000,6089,4051,893.06,31.895,28,730,0.000246,3360,0.346\r\n10.1103/PhysRevB.81.125205,0.00135,-90,0.24,La3Te3.35Sb0.65,\"solid state reaction, Ar\",polycrystalline,400,1.36,131.9,463400000,6293,3990,893.06,31.895,28,741,0.000599,8080,0.532\r\n10.1103/PhysRevB.81.125205,0.00535,-70,0.04,La3Te3.35Bi0.65,\"solid state reaction, Ar\",polycrystalline,400,1.83,140,444300000,6025,4313,893.06,31.895,28,187,9.03E-05,4830,0.1\r\n10.1103/PhysRevB.81.125205,0.00061,-42,0.11,La2.99Te4,\"solid state reaction, Ar\",polycrystalline,400,2.605,132.44,551400000,5846,4124,893.06,31.895,28,1640,0.000284,1730,0.614\r\n10.1103/PhysRevB.81.125205,0.00268,-89,0.12,La2.74Te4,\"solid state reaction, Ar\",polycrystalline,400,1.17,132.2,572900000,5704,4163,893.06,31.895,28,373,0.000296,7920,0.311\r\n10.1103/PhysRevB.81.125205,0.000802,-68,0.4,La3Te3.8Sb0.2,\"solid state reaction, Ar\",polycrystalline,700,2.72,132.28,523800000,5987,4082,893.06,31.895,28,1250,0.00057,4570,0.783\r\n10.1103/PhysRevB.81.125205,0.00187,-87,0.28,La3Te3.65Sb0.35,\"solid state reaction, Ar\",polycrystalline,700,1.98,132.15,503700000,6089,4051,893.06,31.895,28,535,0.000407,7600,0.461\r\n10.1103/PhysRevB.81.125205,0.00721,-159,0.25,La3Te3.35Sb0.65,\"solid state reaction, Ar\",polycrystalline,700,1.17,131.9,463400000,6293,3990,893.06,31.895,28,139,0.000352,25400,0.202\r\n10.1103/PhysRevB.81.125205,0.00437,-131,0.27,La3Te3.35Bi0.65,\"solid state reaction, Ar\",polycrystalline,700,1.56,140,444300000,6025,4313,893.06,31.895,28,229,0.00039,17100,0.251\r\n10.1103/PhysRevB.81.125205,0.000802,-58,0.29,La2.99Te4,\"solid state reaction, Ar\",polycrystalline,700,2.84,132.44,551400000,5846,4124,893.06,31.895,28,1250,0.000414,3320,0.75\r\n10.1103/PhysRevB.81.125205,0.00425,-159,0.42,La2.74Te4,\"solid state reaction, Ar\",polycrystalline,700,1,132.2,572900000,5704,4163,893.06,31.895,28,235,0.000595,25300,0.402\r\n10.1103/PhysRevB.81.125205,0.00103,-88,0.75,La3Te3.8Sb0.2,\"solid state reaction, Ar\",polycrystalline,1000,2.66,132.28,523800000,5987,4082,893.06,31.895,28,971,0.000748,7710,0.891\r\n10.1103/PhysRevB.81.125205,0.00225,-117,0.61,La3Te3.65Sb0.35,\"solid state reaction, Ar\",polycrystalline,1000,1.85,132.15,503700000,6089,4051,893.06,31.895,28,444,0.000612,13800,0.586\r\n10.1103/PhysRevB.81.125205,0.00687,-221,0.71,La3Te3.35Sb0.65,\"solid state reaction, Ar\",polycrystalline,1000,0.987,131.9,463400000,6293,3990,893.06,31.895,28,146,0.000712,48900,0.36\r\n10.1103/PhysRevB.81.125205,0.00527,-185,0.65,La3Te3.35Bi0.65,\"solid state reaction, Ar\",polycrystalline,1000,1.37,140,444300000,6025,4313,893.06,31.895,28,190,0.000651,34300,0.338\r\n10.1103/PhysRevB.81.125205,0.000974,-75,0.57,La2.99Te4,\"solid state reaction, Ar\",polycrystalline,1000,2.87,132.44,551400000,5846,4124,893.06,31.895,28,1030,0.000573,5580,0.873\r\n10.1103/PhysRevB.81.125205,0.00639,-215,0.72,La2.74Te4,\"solid state reaction, Ar\",polycrystalline,1000,0.893,132.2,572900000,5704,4163,893.06,31.895,28,156,0.000723,46200,0.428\r\n10.1103/PhysRevLett.69.2975,0.00818,150,0.08,La1.95Sr0.05Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,300,,57.54,20920,6746,2457,380.25,13.58,28,122,0.000275,22500,\r\n10.1103/PhysRevLett.69.2975,0.0028,55,0.03,La1.9Sr0.1Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,300,,57.17,20610,6670,2451,378.4,13.514,28,357,0.000107,2990,\r\n10.1103/PhysRevLett.69.2975,0.00113,25,0.02,La1.85Sr0.15Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,300,,56.81,20290,6594,2445,190.07,13.576,14,887,5.55E-05,625,\r\n10.1103/PhysRevLett.69.2975,0.000471,0,1.59E-05,La1.725Sr0.28Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,300,,55.92,19470,6396,2431,190.07,13.576,14,2120,5.30E-08,0.25,\r\n10.1103/PhysRevLett.69.2975,0.011,140,0.07,La1.95Sr0.05Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,400,,57.54,20920,6746,2457,380.25,13.58,28,92.6,0.000182,19600,\r\n10.1103/PhysRevLett.69.2975,0.00382,50,0.03,La1.9Sr0.1Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,400,,57.17,20610,6670,2451,378.4,13.514,28,262,6.55E-05,2500,\r\n10.1103/PhysRevLett.69.2975,0.00149,20,0.01,La1.85Sr0.15Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,400,,56.81,20290,6594,2445,190.07,13.576,14,672,2.69E-05,400,\r\n10.1103/PhysRevLett.69.2975,0.000676,0,5.92E-07,La1.725Sr0.28Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,400,,55.92,19470,6396,2431,190.07,13.576,14,1480,1.48E-09,0.01,\r\n10.1103/PhysRevLett.69.2975,0.016,120,0.06,La1.95Sr0.05Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,700,,57.54,20920,6746,2457,380.25,13.58,28,63.1,9.09E-05,14400,\r\n10.1103/PhysRevLett.69.2975,0.00608,40,0.02,La1.9Sr0.1Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,700,,57.17,20610,6670,2451,378.4,13.514,28,164,2.63E-05,1600,\r\n10.1103/PhysRevLett.69.2975,0.00254,2,0.000133,La1.85Sr0.15Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,700,,56.81,20290,6594,2445,190.07,13.576,14,394,1.91E-07,4.84,\r\n10.1103/PhysRevLett.69.2975,0.00136,0,5.14E-07,La1.725Sr0.28Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,700,,55.92,19470,6396,2431,190.07,13.576,14,735,7.35E-10,0.01,\r\n10.1103/PhysRevLett.69.2975,0.019,100,0.05,La1.95Sr0.05Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,1000,,57.54,20920,6746,2457,380.25,13.58,28,52.1,5.21E-05,10000,\r\n10.1103/PhysRevLett.69.2975,0.00818,30,0.01,La1.9Sr0.1Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,1000,,57.17,20610,6670,2451,378.4,13.514,28,122,1.10E-05,900,\r\n10.1103/PhysRevLett.69.2975,0.00376,1,2.66E-05,La1.85Sr0.15Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,1000,,56.81,20290,6594,2445,190.07,13.576,14,266,2.66E-08,1,\r\n10.1103/PhysRevLett.69.2975,0.00223,0,4.49E-07,La1.725Sr0.28Cu1O4,Solid state reaction (O2 atmosphere),polycrystalline,1000,,55.92,19470,6396,2431,190.07,13.576,14,449,4.49E-10,0.01,\r\n10.1103/PhysRevLett.86.4350,0.00642,256,0.31,Tl9Bi1Te6,\"melted, zone refined\",polycrystalline,300,0.481,175.88,277400000,5429,6036,1025.05,32.033,32,156,0.00102,65500,0.237\r\n10.1103/PhysRevLett.86.4350,0.011,338,0.41,Tl9Bi1Te6,\"melted, zone refined\",polycrystalline,400,0.409,175.88,277400000,5429,6036,1025.05,32.033,32,89.5,0.00102,114000,0.214\r\n10.1109/ICT.1996.553263,0.00391,126,0.12,Ce1Fe2Co2Sb12,combination of melting and powder metallurgy techniques,polycrystalline,300,,107.69,3994000,7379,3223,747,21.971,34,256,0.000406,15900,\r\n10.1109/ICT.1996.553263,0.00103,101,0.3,Ce1Fe3Co1Sb12,combination of melting and powder metallurgy techniques,polycrystalline,300,1.91,107.51,4000000,7367,3185,756.81,22.259,34,971,0.00099,10200,0.372\r\n10.1109/ICT.1996.553263,0.000893,87,0.26,Ce1Fe3.5Co0.5Sb12,combination of melting and powder metallurgy techniques,polycrystalline,300,2.4,107.42,4002000,7361,3165,756.81,22.259,34,1120,0.000851,7600,0.342\r\n10.1109/ICT.1996.553263,0.000771,58,0.13,Ce1Fe4Sb12,combination of melting and powder metallurgy techniques,polycrystalline,300,1.55,107.33,4005000,7355,3146,762.5,22.426,34,1300,0.000439,3390,0.613\r\n10.1109/ICT.1996.553263,0.00385,154,0.25,Ce1Fe2Co2Sb12,combination of melting and powder metallurgy techniques,polycrystalline,400,,107.69,3994000,7379,3223,747,21.971,34,260,0.000616,23700,\r\n10.1109/ICT.1996.553263,0.00112,127,0.58,Ce1Fe3Co1Sb12,combination of melting and powder metallurgy techniques,polycrystalline,400,1.98,107.51,4000000,7367,3185,756.81,22.259,34,893,0.00144,16100,0.44\r\n10.1109/ICT.1996.553263,0.000971,107,0.47,Ce1Fe3.5Co0.5Sb13,combination of melting and powder metallurgy techniques,polycrystalline,400,2.38,108.22,4065000,7395,3181,756.81,22.259,34,1030,0.00118,11400,0.422\r\n10.1109/ICT.1996.553263,0.000836,76,0.27,Ce1Fe4Sb12,combination of melting and powder metallurgy techniques,polycrystalline,400,1.57,107.33,4005000,7355,3146,762.5,22.426,34,1200,0.000685,5730,0.744\r\n10.1109/ICT.1996.553263,0.00325,166,0.59,Ce1Fe2Co2Sb12,combination of melting and powder metallurgy techniques,polycrystalline,700,,107.69,3994000,7379,3223,747,21.971,34,308,0.000848,27600,\r\n10.1109/ICT.1996.553263,0.00129,176,1.68,Ce1Fe3Co1Sb12,combination of melting and powder metallurgy techniques,polycrystalline,700,2.07,107.51,4000000,7367,3185,756.81,22.259,34,775,0.0024,31000,0.64\r\n10.1109/ICT.1996.553263,0.00107,158,1.63,Ce1Fe3.5Co0.5Sb14,combination of melting and powder metallurgy techniques,polycrystalline,700,2.49,108.93,4120000,7425,3195,756.81,22.259,34,935,0.00233,25000,0.641\r\n10.1109/ICT.1996.553263,0.000886,127,1.27,Ce1Fe4Sb12,combination of melting and powder metallurgy techniques,polycrystalline,700,1.703,107.33,4005000,7355,3146,762.5,22.426,34,1130,0.00182,16100,1.132\r\n10.1109/ICT.1999.843362,0.011,-189,0.1,Ba8Ga16Sn30,\"melted, Ar\",polycrystalline,300,,106.95,284700,3226,1823,1595.46,29.546,54,90.1,0.00032,35600,\r\n10.1109/ICT.1999.843362,0.000786,-72,0.2,Sr8Ga16Ge30,\"melted, Ar\",polycrystalline,300,,73.99,391300,5141,2089,1233.18,22.837,54,1270,0.000658,5170,\r\n10.1109/ICT.1999.843362,0.000669,-62,0.17,Ba8Ga16Ge30,\"melted, Ar\",polycrystalline,300,,81.36,356000,4753,2008,1254.12,23.224,54,1490,0.000575,3840,\r\n10.1109/ICT.1999.843362,0.00122,-49,0.06,Ba8Ga16Si30,\"melted, Ar\",polycrystalline,300,,56.61,20060,4373,1811,1254.12,23.224,54,820,0.000199,2430,\r\n10.1109/ICT.1999.843362,0.012,-233,0.19,Ba8Ga16Sn30,\"melted, Ar\",polycrystalline,400,,106.95,284700,3226,1823,1595.46,29.546,54,87,0.000472,54300,\r\n10.1109/ICT.1999.843362,0.000914,-95,0.39,Sr8Ga16Ge30,\"melted, Ar\",polycrystalline,400,,73.99,391300,5141,2089,1233.18,22.837,54,1090,0.000985,9010,\r\n10.1109/ICT.1999.843362,0.00084,-101,0.48,Ba8Ga16Ge30,\"melted, Ar\",polycrystalline,400,,81.36,356000,4753,2008,1254.12,23.224,54,1190,0.00121,10200,\r\n10.1109/ICT.1999.843362,0.00133,-63,0.12,Ba8Ga16Si30,\"melted, Ar\",polycrystalline,400,,56.61,20060,4373,1811,1254.12,23.224,54,752,0.000297,3940,\r\n10.1109/ICT.1999.843362,0.00694,-138,0.19,Ba8Ga16Sn30,\"melted, Ar\",polycrystalline,700,,106.95,284700,3226,1823,1595.46,29.546,54,144,0.000274,19000,\r\n10.1109/ICT.1999.843362,0.00141,-139,0.96,Sr8Ga16Ge30,\"melted, Ar\",polycrystalline,700,,73.99,391300,5141,2089,1233.18,22.837,54,709,0.00137,19300,\r\n10.1109/ICT.1999.843362,0.00141,-186,1.72,Ba8Ga16Ge30,\"melted, Ar\",polycrystalline,700,,81.36,356000,4753,2008,1254.12,23.224,54,709,0.00245,34600,\r\n10.1109/ICT.1999.843362,0.00187,-111,0.46,Ba8Ga16Si30,\"melted, Ar\",polycrystalline,700,,56.61,20060,4373,1811,1254.12,23.224,54,535,0.000659,12300,\r\n10.1109/ICT.2002.1190269,0.00282,149,0.24,Ba8Ga16Ge30,arc melting,polycrystalline,300,2,81.36,356000,4753,2008,1254.12,23.224,54,355,0.000788,22200,0.13\r\n10.1109/ICT.2002.1190269,0.00776,-79,0.02,Ba8Ga18Ge28,arc melting,polycrystalline,300,1.5,81.25,335300,4759,2008,1254.12,23.224,54,129,8.02E-05,6230,0.063\r\n10.1109/ICT.2002.1190269,0.00305,185,0.45,Ba8Ga16Ge30,arc melting,polycrystalline,400,2,81.36,356000,4753,2008,1254.12,23.224,54,328,0.00112,34200,0.16\r\n10.1109/ICT.2002.1190269,0.00714,-113,0.07,Ba8Ga18Ge28,arc melting,polycrystalline,400,1.4,81.25,335300,4759,2008,1254.12,23.224,54,140,0.000178,12700,0.098\r\n10.1109/ICT.2002.1190269,0.00463,288,1.25,Ba8Ga16Ge30,arc melting,polycrystalline,700,2,81.36,356000,4753,2008,1254.12,23.224,54,216,0.00179,82900,0.184\r\n10.1109/ICT.2002.1190269,0.00742,-219,0.45,Ba8Ga18Ge28,arc melting,polycrystalline,700,1.1,81.25,335300,4759,2008,1254.12,23.224,54,135,0.000647,48000,0.209\r\n10.1109/ICT.2002.1190269,0.00625,289,1.34,Ba8Ga16Ge30,arc melting,polycrystalline,1000,2,81.36,356000,4753,2008,1254.12,23.224,54,160,0.00134,83500,0.195\r\n10.1109/ICT.2002.1190269,0.00735,-266,0.96,Ba8Ga18Ge28,arc melting,polycrystalline,1000,1,81.25,335300,4759,2008,1254.12,23.224,54,136,0.000963,70800,0.332\r\n10.1109/ICT.2006.331288,18.4,1235,0.00249,Cu1Cr1O2,\"solid state reaction, air\",polycrystalline,300,6.586,36.88,8516,1881,2193,131.06,10.922,12,0.054,8.31E-06,1530000,6.05E-06\r\n10.1109/ICT.2006.331288,6.112,525,0.00135,Cu1Cr0.99Mg0.01O2,\"solid state reaction, air\",polycrystalline,300,6.966,36.82,8514,1882,2184,131.06,10.922,12,0.164,4.51E-06,276000,1.72E-05\r\n10.1109/ICT.2006.331288,1.045,312,0.00279,Cu1Cr0.98Mg0.02O2,\"solid state reaction, air\",polycrystalline,300,7.558,36.75,8512,1883,2174,131.12,10.927,12,0.957,9.29E-06,97100,9.27E-05\r\n10.1109/ICT.2006.331288,0.102,199,0.01,Cu1Cr0.97Mg0.03O2,\"solid state reaction, air\",polycrystalline,300,7.14,36.68,8511,1885,2165,131.14,10.928,12,9.829,3.89E-05,39600,0.00101\r\n10.1109/ICT.2006.331288,0.107,197,0.01,Cu1Cr0.96Mg0.04O2,\"solid state reaction, air\",polycrystalline,300,9.293,36.61,8509,1886,2156,131.2,10.933,12,9.374,3.63E-05,38700,0.000738\r\n10.1109/ICT.2006.331288,0.075,208,0.02,Cu1Cr0.95Mg0.05O2,\"solid state reaction, air\",polycrystalline,300,9.522,36.54,8507,1887,2146,131.16,10.93,12,13.3,5.74E-05,43300,0.00102\r\n10.1109/ICT.2006.331288,18.7,916,0.0018,Cu1Cr1O2,\"solid state reaction, air\",polycrystalline,400,6.156,36.88,8516,1881,2193,131.06,10.922,12,0.054,4.49E-06,840000,8.49E-06\r\n10.1109/ICT.2006.331288,1.758,445,0.0045,Cu1Cr0.99Mg0.01O2,\"solid state reaction, air\",polycrystalline,400,6.403,36.82,8514,1882,2184,131.06,10.922,12,0.569,1.13E-05,198000,8.67E-05\r\n10.1109/ICT.2006.331288,0.569,332,0.00775,Cu1Cr0.98Mg0.02O2,\"solid state reaction, air\",polycrystalline,400,6.709,36.75,8512,1883,2174,131.12,10.927,12,1.757,1.94E-05,110000,0.000256\r\n10.1109/ICT.2006.331288,0.069,241,0.03,Cu1Cr0.97Mg0.03O2,\"solid state reaction, air\",polycrystalline,400,6.461,36.68,8511,1885,2165,131.14,10.928,12,14.4,8.40E-05,58200,0.00218\r\n10.1109/ICT.2006.331288,0.066,225,0.03,Cu1Cr0.96Mg0.04O2,\"solid state reaction, air\",polycrystalline,400,8.767,36.61,8509,1886,2156,131.2,10.933,12,15.1,7.68E-05,50800,0.00168\r\n10.1109/ICT.2006.331288,0.055,241,0.04,Cu1Cr0.95Mg0.05O2,\"solid state reaction, air\",polycrystalline,400,9.016,36.54,8507,1887,2146,131.16,10.93,12,18.3,0.000107,58200,0.00198\r\n10.1109/ICT.2006.331288,3.408,634,0.00825,Cu1Cr1O2,\"solid state reaction, air\",polycrystalline,700,4.884,36.88,8516,1881,2193,131.06,10.922,12,0.293,1.18E-05,402000,0.000103\r\n10.1109/ICT.2006.331288,0.472,428,0.03,Cu1Cr0.99Mg0.01O2,\"solid state reaction, air\",polycrystalline,700,5.704,36.82,8514,1882,2184,131.06,10.922,12,2.118,3.88E-05,183000,0.000634\r\n10.1109/ICT.2006.331288,0.265,368,0.04,Cu1Cr0.98Mg0.02O2,\"solid state reaction, air\",polycrystalline,700,5.838,36.75,8512,1883,2174,131.12,10.927,12,3.772,5.11E-05,135000,0.0011\r\n10.1109/ICT.2006.331288,0.049,290,0.12,Cu1Cr0.97Mg0.03O2,\"solid state reaction, air\",polycrystalline,700,5.666,36.68,8511,1885,2165,131.14,10.928,12,20.6,0.000173,83900,0.00621\r\n10.1109/ICT.2006.331288,0.047,270,0.11,Cu1Cr0.96Mg0.04O2,\"solid state reaction, air\",polycrystalline,700,7.973,36.61,8509,1886,2156,131.2,10.933,12,21.3,0.000156,73000,0.00457\r\n10.1109/ICT.2006.331288,0.041,282,0.14,Cu1Cr0.95Mg0.05O2,\"solid state reaction, air\",polycrystalline,700,8.087,36.54,8507,1887,2146,131.16,10.93,12,24.6,0.000195,79300,0.00519\r\n10.1109/ICT.2006.331288,1.664,617,0.02,Cu1Cr1O2,\"solid state reaction, air\",polycrystalline,1000,3.708,36.88,8516,1881,2193,131.06,10.922,12,0.601,2.29E-05,381000,0.000395\r\n10.1109/ICT.2006.331288,0.366,446,0.05,Cu1Cr0.99Mg0.01O2,\"solid state reaction, air\",polycrystalline,1000,4.948,36.82,8514,1882,2184,131.06,10.922,12,2.732,5.43E-05,199000,0.00135\r\n10.1109/ICT.2006.331288,0.232,404,0.07,Cu1Cr0.98Mg0.02O2,\"solid state reaction, air\",polycrystalline,1000,4.833,36.75,8512,1883,2174,131.12,10.927,12,4.307,7.02E-05,163000,0.00217\r\n10.1109/ICT.2006.331288,0.047,325,0.22,Cu1Cr0.97Mg0.03O2,\"solid state reaction, air\",polycrystalline,1000,4.776,36.68,8511,1885,2165,131.14,10.928,12,21.3,0.000225,106000,0.011\r\n10.1109/ICT.2006.331288,0.044,304,0.21,Cu1Cr0.96Mg0.04O2,\"solid state reaction, air\",polycrystalline,1000,6.854,36.61,8509,1886,2156,131.2,10.933,12,22.6,0.000208,92300,0.00804\r\n10.1109/ICT.2006.331288,0.041,325,0.26,Cu1Cr0.95Mg0.05O2,\"solid state reaction, air\",polycrystalline,1000,6.988,36.54,8507,1887,2146,131.16,10.93,12,24.5,0.000259,106000,0.00856\r\n10.1109/ICT.2006.331289,0.00249,139,0.23,Cu1Rh0.9Mg0.1O2,\"solid state reaction, air\",polycrystalline,300,,47.65,485900000,2250,4486,140.56,11.713,12,402,0.000774,19300,\r\n10.1109/ICT.2006.331289,0.0027,153,0.35,Cu1Rh0.9Mg0.1O2,\"solid state reaction, air\",polycrystalline,400,9.767,47.65,485900000,2250,4486,140.56,11.713,12,370,0.000867,23400,0.037\r\n10.1109/ICT.2006.331289,0.00392,203,0.74,Cu1Rh0.9Mg0.1O2,\"solid state reaction, air\",polycrystalline,700,10.01,47.65,485900000,2250,4486,140.56,11.713,12,255,0.00105,41200,0.044\r\n10.1109/ICT.2006.331289,0.00553,266,1.28,Cu1Rh0.9Mg0.1O2,\"solid state reaction, air\",polycrystalline,1000,8.392,47.65,485900000,2250,4486,140.56,11.713,12,181,0.00128,70800,0.053\r\n10.1109/ICT.2006.331291,0.303,-651,0.04,Ca1Mn1O3,Solid state reaction,polycrystalline,300,3.562,28.6,398,1861,1276,206.97,10.348,20,3.305,0.00014,424000,0.000679\r\n10.1109/ICT.2006.331291,0.00919,-109,0.04,Ca1Yb0.05Mn0.95O3,Solid state reaction,polycrystalline,300,1.49,29.78,19730,2309,1374,206.97,10.348,20,109,0.00013,11900,0.053\r\n10.1109/ICT.2006.331291,0.0039,-53,0.02,Ca1Yb0.1Mn0.9O3,Solid state reaction,polycrystalline,300,1.725,30.96,37590,2722,1465,207.52,10.376,20,256,7.15E-05,2790,0.109\r\n10.1109/ICT.2006.331291,0.00336,-38,0.01,Ca1Yb0.15Mn0.85O3,Solid state reaction,polycrystalline,300,1.645,32.15,54140,3105,1549,207.52,10.376,20,297,4.35E-05,1460,0.132\r\n10.1109/ICT.2006.331291,0.015,-9,0.000163,Ca1Yb0.4Mn0.6O3,Solid state reaction,polycrystalline,300,,38.05,121500,4663,1891,207.52,10.376,20,65.7,5.45E-07,82.9,\r\n10.1109/ICT.2006.331291,0.242,-587,0.06,Ca1Mn1O3,Solid state reaction,polycrystalline,400,3.067,28.6,398,1861,1276,206.97,10.348,20,4.138,0.000143,345000,0.00132\r\n10.1109/ICT.2006.331291,0.011,-125,0.06,Ca1Yb0.05Mn0.95O3,Solid state reaction,polycrystalline,400,1.472,29.78,19730,2309,1374,206.97,10.348,20,94.3,0.000147,15600,0.063\r\n10.1109/ICT.2006.331291,0.00438,-60,0.03,Ca1Yb0.1Mn0.9O3,Solid state reaction,polycrystalline,400,1.639,30.96,37590,2722,1465,207.52,10.376,20,228,8.24E-05,3610,0.136\r\n10.1109/ICT.2006.331291,0.00359,-49,0.03,Ca1Yb0.15Mn0.85O3,Solid state reaction,polycrystalline,400,1.571,32.15,54140,3105,1549,207.52,10.376,20,279,6.73E-05,2420,0.173\r\n10.1109/ICT.2006.331291,0.012,-20,0.00133,Ca1Yb0.4Mn0.6O3,Solid state reaction,polycrystalline,400,,38.05,121500,4663,1891,207.52,10.376,20,82.8,3.32E-06,401,\r\n10.1109/ICT.2006.331291,0.103,-362,0.09,Ca1Mn1O3,Solid state reaction,polycrystalline,700,2.158,28.6,398,1861,1276,206.97,10.348,20,9.699,0.000127,131000,0.00768\r\n10.1109/ICT.2006.331291,0.016,-168,0.13,Ca1Yb0.05Mn0.95O3,Solid state reaction,polycrystalline,700,1.602,29.78,19730,2309,1374,206.97,10.348,20,64.2,0.000182,28400,0.068\r\n10.1109/ICT.2006.331291,0.00615,-85,0.08,Ca1Yb0.1Mn0.9O3,Solid state reaction,polycrystalline,700,1.614,30.96,37590,2722,1465,207.52,10.376,20,163,0.000117,7170,0.172\r\n10.1109/ICT.2006.331291,0.00482,-61,0.05,Ca1Yb0.15Mn0.85O3,Solid state reaction,polycrystalline,700,1.67,32.15,54140,3105,1549,207.52,10.376,20,208,7.72E-05,3720,0.212\r\n10.1109/ICT.2006.331291,0.011,-51,0.02,Ca1Yb0.4Mn0.6O3,Solid state reaction,polycrystalline,700,,38.05,121500,4663,1891,207.52,10.376,20,94.2,2.45E-05,2600,\r\n10.1109/ICT.2006.331291,0.084,-282,0.09,Ca1Mn1O3,Solid state reaction,polycrystalline,1000,2.065,28.6,398,1861,1276,206.97,10.348,20,11.9,9.44E-05,79600,0.014\r\n10.1109/ICT.2006.331291,0.019,-245,0.32,Ca1Yb0.05Mn0.95O3,Solid state reaction,polycrystalline,1000,1.614,29.78,19730,2309,1374,206.97,10.348,20,53.6,0.000321,60000,0.081\r\n10.1109/ICT.2006.331291,0.00782,-128,0.21,Ca1Yb0.1Mn0.9O3,Solid state reaction,polycrystalline,1000,1.583,30.96,37590,2722,1465,207.52,10.376,20,128,0.000211,16500,0.197\r\n10.1109/ICT.2006.331291,0.00596,-101,0.17,Ca1Yb0.15Mn0.85O3,Solid state reaction,polycrystalline,1000,1.694,32.15,54140,3105,1549,207.52,10.376,20,168,0.000171,10200,0.242\r\n10.1109/ICT.2006.331291,0.011,-25,0.00586,Ca1Yb0.4Mn0.6O3,Solid state reaction,polycrystalline,1000,,38.05,121500,4663,1891,207.52,10.376,20,90.3,5.86E-06,650,\r\n10.1109/ICT.2007.4569450,0.00604,-139,0.13,Ca0.96Sm0.04Mn1O3,Co-precipitation,polycrystalline,400,,29.48,6638,2150,1349,210.39,10.519,20,166,0.000322,19400,\r\n10.1109/ICT.2007.4569450,0.00825,-170,0.24,Ca0.96Sm0.04Mn1O3,Co-precipitation,polycrystalline,700,,29.48,6638,2150,1349,210.39,10.519,20,121,0.00035,28900,\r\n10.1109/ICT.2007.4569450,0.011,-188,0.32,Ca0.96Sm0.04Mn1O3,Co-precipitation,polycrystalline,1000,,29.48,6638,2150,1349,210.39,10.519,20,90.5,0.000318,35200,\r\n10.1111/j.1551-2916.2010.03673.x,0.031,-212,0.04,Ca1Gd0.98Mn0.02O3,Co-precipitation,polycrystalline,300,,48.66,111100,6744,2336,210.36,10.518,20,32.7,0.000147,44900,\r\n10.1111/j.1551-2916.2010.03673.x,0.015,-162,0.05,Ca1Gd0.96Mn0.04O3,Co-precipitation,polycrystalline,300,1.787,48.25,109800,6685,2323,210.36,10.518,20,67.3,0.000177,26400,0.028\r\n10.1111/j.1551-2916.2010.03673.x,0.015,-104,0.02,Ca1Gd0.94Mn0.06O3,Co-precipitation,polycrystalline,300,2.85,47.84,108400,6625,2310,210.36,10.518,20,68.8,7.48E-05,10900,0.018\r\n10.1111/j.1551-2916.2010.03673.x,0.028,-215,0.07,Ca1Gd0.98Mn0.02O3,Co-precipitation,polycrystalline,400,,48.66,111100,6744,2336,210.36,10.518,20,36.3,0.000168,46400,\r\n10.1111/j.1551-2916.2010.03673.x,0.013,-164,0.08,Ca1Gd0.96Mn0.04O3,Co-precipitation,polycrystalline,400,1.615,48.25,109800,6685,2323,210.36,10.518,20,77.7,0.000208,26700,0.047\r\n10.1111/j.1551-2916.2010.03673.x,0.011,-119,0.05,Ca1Gd0.94Mn0.06O3,Co-precipitation,polycrystalline,400,2.57,47.84,108400,6625,2310,210.36,10.518,20,88.1,0.000124,14000,0.033\r\n10.1111/j.1551-2916.2010.03673.x,0.022,-228,0.16,Ca1Gd0.98Mn0.02O3,Co-precipitation,polycrystalline,700,,48.66,111100,6744,2336,210.36,10.518,20,45.2,0.000235,51900,\r\n10.1111/j.1551-2916.2010.03673.x,0.012,-173,0.18,Ca1Gd0.96Mn0.04O3,Co-precipitation,polycrystalline,700,1.346,48.25,109800,6685,2323,210.36,10.518,20,85.7,0.000255,29800,0.109\r\n10.1111/j.1551-2916.2010.03673.x,0.00866,-145,0.17,Ca1Gd0.94Mn0.06O3,Co-precipitation,polycrystalline,700,2.139,47.84,108400,6625,2310,210.36,10.518,20,115,0.000242,20900,0.092\r\n10.1111/j.1551-2916.2010.03673.x,0.023,-235,0.24,Ca1Gd0.98Mn0.02O3,Co-precipitation,polycrystalline,1000,,48.66,111100,6744,2336,210.36,10.518,20,44,0.000244,55400,\r\n10.1111/j.1551-2916.2010.03673.x,0.011,-173,0.28,Ca1Gd0.96Mn0.04O3,Co-precipitation,polycrystalline,1000,1.28,48.25,109800,6685,2323,210.36,10.518,20,94.6,0.000282,29800,0.18\r\n10.1111/j.1551-2916.2010.03673.x,0.00887,-145,0.24,Ca1Gd0.94Mn0.06O3,Co-precipitation,polycrystalline,1000,1.945,47.84,108400,6625,2310,210.36,10.518,20,113,0.000236,20900,0.141\r\n10.1111/j.1551-2916.2012.05169.x,0.00114,-19,0.0095,Sr4.5Nb4.5O15.5,\"floating zone method, Ar\",single crystal,300,2.45,43.28,22330,5032,4699,735.99,14.154,52,877,3.17E-05,361,0.262\r\n10.1111/j.1551-2916.2012.05169.x,0.005,-107,0.07,Sr1.6La0.4Nb2O7,\"floating zone method, Ar\",single,300,1.8,44.87,24210,5577,4628,597.36,13.576,44,200,0.000229,11400,0.081\r\n10.1126/science.1159725,0.00274,140,0.22,Tl0.01Pb0.99Te1,melted,polycrystalline,300,1.942,167.39,381200000,2806,3012,269.84,33.73,8,365,0.000719,19700,0.137\r\n10.1126/science.1159725,0.00239,136,0.23,Tl0.02Pb0.98Te1,melted,polycrystalline,300,2.168,167.37,381300000,2829,3041,269.84,33.73,8,418,0.000775,18500,0.141\r\n10.1126/science.1159725,0.00355,201,0.46,Tl0.01Pb0.99Te1,melted,polycrystalline,400,1.552,167.39,381200000,2806,3012,269.84,33.73,8,282,0.00114,40600,0.177\r\n10.1126/science.1159725,0.00291,195,0.52,Tl0.02Pb0.98Te1,melted,polycrystalline,400,1.656,167.37,381300000,2829,3041,269.84,33.73,8,344,0.00131,38100,0.203\r\n10.1126/science.1159725,0.00873,324,0.84,Tl0.01Pb0.99Te1,melted,polycrystalline,700,0.965,167.39,381200000,2806,3012,269.84,33.73,8,115,0.0012,105000,0.203\r\n10.1126/science.1159725,0.00536,328,1.4,Tl0.02Pb0.98Te1,melted,polycrystalline,700,1.01,167.37,381300000,2829,3041,269.84,33.73,8,186,0.002,107000,0.315\r\n10.1126/science.287.5455.1024,0.000774,105,0.43,Cs1Bi4Te6,\"melted, air\",single crystal,300,,157.68,469800000,4289,5526,3250.47,36.937,88,1290,0.00143,11100,\r\n10.1126/science.287.5455.1024,0.00085,154,0.84,Sb0.005I0.015Cs0.995Bi3.98Te5.97,\"melted, air\",single crystal,300,1.5,157.62,469100000,4291,5525,3250.47,36.937,88,1180,0.0028,23800,0.574\r\n10.1143/JJAP.38.L1336,28.9,295,0.000121,Li0.0024Ni0.9976O1,Solid state reaction,polycrystalline,400,16.172,37.28,6484,883.7,1270,72.93,9.116,8,0.035,3.01E-07,87000,2.09E-06\r\n10.1143/JJAP.38.L1336,5.086,249,0.000489,Li0.0066Ni0.9944O1,Solid state reaction,polycrystalline,400,8.328,37.19,6498,884.2,1270,72.93,9.116,8,0.197,1.22E-06,62200,2.30E-05\r\n10.1143/JJAP.38.L1336,0.064,117,0.00851,Li0.0184Ni0.9816O1,Solid state reaction,polycrystalline,400,,36.87,6533,885.3,1271,72.93,9.116,8,15.6,2.13E-05,13700,\r\n10.1143/JJAP.38.L1336,0.012,103,0.03,Li0.0242Ni0.9758O1,Solid state reaction,polycrystalline,400,3.751,36.72,6552,885.9,1272,72.93,9.116,8,81,8.53E-05,10500,0.021\r\n10.1143/JJAP.38.L1336,153,483,0.000107,Ni1O1,Solid state reaction,polycrystalline,700,,37.35,6477,883.5,1269,72.93,9.116,8,0.00654,1.53E-07,234000,\r\n10.1143/JJAP.38.L1336,0.263,250,0.02,Li0.0024Ni0.9976O1,Solid state reaction,polycrystalline,700,11.391,37.28,6484,883.7,1270,72.93,9.116,8,3.804,2.37E-05,62400,0.00057\r\n10.1143/JJAP.38.L1336,0.032,200,0.09,Li0.0066Ni0.9944O1,Solid state reaction,polycrystalline,700,6.01,37.19,6498,884.2,1270,72.93,9.116,8,31.6,0.000127,40200,0.00899\r\n10.1143/JJAP.38.L1336,0.02,98,0.03,Li0.0184Ni0.9816O1,Solid state reaction,polycrystalline,700,,36.87,6533,885.3,1271,72.93,9.116,8,50.5,4.84E-05,9580,\r\n10.1143/JJAP.38.L1336,0.00487,77,0.09,Li0.0242Ni0.9758O1,Solid state reaction,polycrystalline,700,3.496,36.72,6552,885.9,1272,72.93,9.116,8,206,0.000123,5990,0.1\r\n10.1143/JJAP.38.L1336,14.6,643,0.00282,Ni1O1,Solid state reaction,polycrystalline,1000,,37.35,6477,883.5,1269,72.93,9.116,8,0.068,2.82E-06,413000,\r\n10.1143/JJAP.38.L1336,0.047,262,0.15,Li0.0024Ni0.9976O1,Solid state reaction,polycrystalline,1000,8.444,37.28,6484,883.7,1270,72.93,9.116,8,21.5,0.000148,68900,0.0062\r\n10.1143/JJAP.38.L1336,0.028,207,0.15,Li0.0066Ni0.9944O1,Solid state reaction,polycrystalline,1000,5.305,37.19,6498,884.2,1270,72.93,9.116,8,35.1,0.00015,42700,0.016\r\n10.1143/JJAP.38.L1336,0.00666,105,0.17,Li0.0184Ni0.9816O1,Solid state reaction,polycrystalline,1000,,36.87,6533,885.3,1271,72.93,9.116,8,150,0.000166,11100,\r\n10.1143/JJAP.38.L1336,0.00387,79,0.16,Li0.0242Ni0.9758O1,Solid state reaction,polycrystalline,1000,2.55,36.72,6552,885.9,1272,72.93,9.116,8,258,0.000163,6320,0.247\r\n10.1143/JJAP.39.L1127,0.00147,135,0.37,Ca2Co2O5,melted,single crystal,300,2.3,30.89,15420,2551,1702,236.38,10.883,21.72,681,0.00124,18200,0.217\r\n10.1143/JJAP.39.L1127,0.00147,142,0.55,Ca2Co2O5,melted,single crystal,400,2.35,30.89,15420,2551,1702,236.38,10.883,21.72,682,0.00138,20300,0.283\r\n10.1143/JJAP.39.L1127,0.00145,173,1.46,Ca2Co2O5,melted,single crystal,700,2.6,30.89,15420,2551,1702,236.38,10.883,21.72,691,0.00208,30100,0.454\r\n10.1143/JJAP.39.L1127,0.00138,207,3.12,Ca2Co2O5,melted,single crystal,1000,2.9,30.89,15420,2551,1702,236.38,10.883,21.72,725,0.00312,43000,0.61\r\n10.1143/JJAP.40.4644,0.000295,82,0.68,Na1Co2O4,\"flux (NaCl), air\",single crystal,300,19.08,29.26,20930,2036,1740,75.67,10.81,7,3390,0.00228,6710,0.13\r\n10.1143/JJAP.40.4644,0.00211,104,0.15,Na1Co2O4,\"solid state reaction, air\",polycrystalline,300,1.904,29.26,20930,2036,1740,75.67,10.81,7,475,0.000514,10800,0.183\r\n10.1143/JJAP.40.4644,0.000354,98,1.09,Na1Co2O4,\"flux (NaCl), air\",single crystal,400,13.53,29.26,20930,2036,1740,75.67,10.81,7,2830,0.00271,9600,0.204\r\n10.1143/JJAP.40.4644,0.00253,118,0.22,Na1Co2O4,\"solid state reaction, air\",polycrystalline,400,1.834,29.26,20930,2036,1740,75.67,10.81,7,395,0.000551,13900,0.21\r\n10.1143/JJAP.40.4644,0.000484,146,3.08,Na1Co2O4,\"flux (NaCl), air\",single crystal,700,5.702,29.26,20930,2036,1740,75.67,10.81,7,2060,0.0044,21300,0.618\r\n10.1143/JJAP.40.4644,0.0034,161,0.53,Na1Co2O4,\"solid state reaction, air\",polycrystalline,700,2.093,29.26,20930,2036,1740,75.67,10.81,7,294,0.000762,25900,0.24\r\n10.1143/JJAP.40.4644,0.0006,200,6.67,Na1Co2O4,\"flux (NaCl), air\",single crystal,1000,4.764,29.26,20930,2036,1740,75.67,10.81,7,1670,0.00667,40000,0.854\r\n10.1143/JJAP.40.4644,0.004,175,0.77,Na1Co2O4,\"solid state reaction, air\",polycrystalline,1000,2.224,29.26,20930,2036,1740,75.67,10.81,7,250,0.000766,30600,0.274\r\n10.1201/9781420049718.ch19,0.00055,162,1.43,Bi2Te3,melted,single crystal,300,1.468,160.15,508700000,4147,5487,509.21,33.947,15,1820,0.00477,26200,0.906\r\n10.1201/9781420049718.ch19,0.00045,-174,2.02,Bi2Te3,melted,single crystal,300,4.017,160.15,508700000,4147,5487,509.21,33.947,15,2220,0.00673,30300,0.405\r\n10.1201/9781420049718.ch19,0.00019,38,0.23,Sb2Te3,melted,single crystal,300,3.378,125.26,613100000,4841,4345,479.59,31.973,15,5260,0.00076,1440,1.141\r\n10.1201/9781420049718.ch19,0.000122,63,0.98,Sb2Te3,melted,single crystal,300,5.205,125.26,613100000,4841,4345,479.59,31.973,15,8200,0.00325,3970,1.153\r\n10.1201/9781420049718.ch22,0.000694,79,0.27,Ag0.15Sb0.15Te1.15Ge0.85,melted,single crystal,300,1.499,105.62,605500000,3762,3810,479.59,31.973,15,1440,0.000891,6190,0.704\r\n10.1201/9781420049718.ch22,0.00085,122,0.7,Ag0.15Sb0.15Te1.15Ge0.85,melted,single crystal,400,1.531,105.62,605500000,3762,3810,479.59,31.973,15,1180,0.00176,14900,0.75\r\n10.1201/9781420049718.ch22,0.00121,199,2.29,Ag0.15Sb0.15Te1.15Ge0.85,melted,single crystal,700,1.651,105.62,605500000,3762,3810,479.59,31.973,15,824,0.00326,39600,0.853\r\n10.1201/9781420049718.ch22,0.00128,166,2.15,Ag0.15Sb0.15Te1.15Ge0.85,melted,single crystal,1000,2.272,105.62,605500000,3762,3810,479.59,31.973,15,784,0.00215,27500,0.842\r\n10.1557/jmr.2010.78,0.062,-220,0.02,Sr0.61Ba0.39Nb2O6,\"templated grain growth, air, anneal PO<sub>2</sub> 10<sup>-14</sup>\",polycrystalline,300,1.667,43.2,26540,5182,5061,610.4,13.564,45,16.2,7.82E-05,48400,0.0071\r\n10.1557/jmr.2010.78,0.016,-220,0.12,Sr0.61Ba0.39Nb2O6,\"templated grain growth, air, anneal PO<sub>2</sub> 10<sup>-14</sup>\",polycrystalline,400,2.02,43.2,26540,5182,5061,610.4,13.564,45,61.6,0.000298,48400,0.03\r\n10.1557/jmr.2010.78,0.008,-216,0.41,Sr0.61Ba0.39Nb2O6,\"templated grain growth, air, anneal PO<sub>2</sub> 10<sup>-14</sup>\",polycrystalline,700,2.172,43.2,26540,5182,5061,610.4,13.564,45,125,0.000583,46700,0.098\r\n10.1557/jmr.2011.140,0.02,-180,0.05,Ca1Mn0.98Nb0.02O3,Ultrasonic Spray Pyrolysis,polycrystalline,300,2.5,28.75,1087,1950,1369,208.21,10.41,20,50,0.000162,32400,0.015\r\n10.1557/jmr.2011.140,0.022,-204,0.08,Ca1Mn0.98Nb0.02O3,Ultrasonic Spray Pyrolysis,polycrystalline,400,2.075,28.75,1087,1950,1369,208.21,10.41,20,46.4,0.000193,41600,0.022\r\n10.1557/jmr.2011.140,0.028,-235,0.14,Ca1Mn0.98Nb0.02O3,Ultrasonic Spray Pyrolysis,polycrystalline,700,1.631,28.75,1087,1950,1369,208.21,10.41,20,35.3,0.000194,55000,0.037\r\n10.1557/jmr.2011.140,0.031,-248,0.2,Ca1Mn0.98Nb0.02O3,Ultrasonic Spray Pyrolysis,polycrystalline,1000,1.381,28.75,1087,1950,1369,208.21,10.41,20,32.4,0.0002,61600,0.057\r\n10.1557/jmr.2011.163,0.00113,-192,0.98,In0.2Co4Sb12,Solid state reaction,polycrystalline,300,2.57,106.16,4318000,7180,3295,742.742,22.924,32.4,882,0.00326,36900,0.251\r\n10.1557/jmr.2011.163,0.00129,-214,1.43,In0.2Co4Sb12,Solid state reaction,polycrystalline,400,2.214,106.16,4318000,7180,3295,742.742,22.924,32.4,777,0.00357,46000,0.342\r\n10.1557/jmr.2011.163,0.0016,-248,2.68,In0.2Co4Sb12,Solid state reaction,polycrystalline,700,1.937,106.16,4318000,7180,3295,742.742,22.924,32.4,626,0.00383,61300,0.552\r\n10.1557/PROC-793-S3.3,0.00284,-20,0.00556,La1Ni1O3,\"Evaporate nitrates (1173 K, air)\",polycrystalline,400,,49.12,17470,5693,2221,339.43,11.314,30,352,1.39E-05,395,\r\n10.1557/PROC-793-S3.3,0.00267,-21,0.00657,La0.9Bi0.1Ni1O3,\"Evaporate nitrates (1173 K, air)\",polycrystalline,400,,50.52,4882000,5452,2483,339.43,11.314,30,374,1.64E-05,439,\r\n10.1557/PROC-793-S3.3,0.0046,-26,0.01,La1Ni1O3,\"Evaporate nitrates (1173 K, air)\",polycrystalline,700,,49.12,17470,5693,2221,339.43,11.314,30,217,1.44E-05,664,\r\n10.1557/PROC-793-S3.3,0.00413,-28,0.01,La0.9Bi0.1Ni1O3,\"Evaporate nitrates (1173 K, air)\",polycrystalline,700,,50.52,4882000,5452,2483,339.43,11.314,30,242,1.96E-05,810,\r\n10.1557/PROC-793-S3.3,0.00622,-27,0.01,La1Ni1O3,\"Evaporate nitrates (1173 K, air)\",polycrystalline,1000,,49.12,17470,5693,2221,339.43,11.314,30,161,1.17E-05,731,\r\n10.1557/PROC-793-S3.3,0.00609,-31,0.02,La0.9Bi0.1Ni1O3,\"Evaporate nitrates (1173 K, air)\",polycrystalline,1000,,50.52,4882000,5452,2483,339.43,11.314,30,164,1.56E-05,948,\r\n10.3390/ma3042606,0.000324,-41,0.16,Bi1.2S1.2Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,300,2.94,61.1,28740000,3036,3543,175.2,20.857,8.4,3090,0.000526,1710,0.768\r\n10.3390/ma3042606,0.00046,-51,0.17,Pb1.8S1.8Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,300,2.9,68.19,48160,1920,1526,175.2,20.857,8.4,2170,0.000561,2580,0.549\r\n10.3390/ma3042606,0.000478,-65,0.26,Sn1.2S1.2Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,300,2.66,48.21,157400,1480,1355,175.2,20.857,8.4,2090,0.000878,4200,0.576\r\n10.3390/ma3042606,0.000499,-55,0.24,Bi1.2S1.2Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,400,2.41,61.1,28740000,3036,3543,175.2,20.857,8.4,2000,0.000603,3010,0.812\r\n10.3390/ma3042606,0.000728,-71,0.28,Pb1.8S1.8Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,400,2.51,68.19,48160,1920,1526,175.2,20.857,8.4,1370,0.000689,5010,0.534\r\n10.3390/ma3042606,0.00085,-89,0.37,Sn1.2S1.2Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,400,2.03,48.21,157400,1480,1355,175.2,20.857,8.4,1180,0.000928,7890,0.566\r\n10.3390/ma3042606,0.000948,-89,0.59,Bi1.2S1.2Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,700,2.11,61.1,28740000,3036,3543,175.2,20.857,8.4,1050,0.000838,7940,0.854\r\n10.3390/ma3042606,0.00217,-129,0.53,Pb1.8S1.8Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,700,1.95,68.19,48160,1920,1526,175.2,20.857,8.4,460,0.000764,16600,0.403\r\n10.3390/ma3042606,0.00217,-141,0.64,Sn1.2S1.2Ti2S4,\"solid-liquid-vapor reaction, vacuum\",polycrystalline,700,1.69,48.21,157400,1480,1355,175.2,20.857,8.4,460,0.000912,19800,0.465\r\n10.1063/1.1562337,0.00197,126,0.24,Ca3Co4O9,\"flux (SrCl2), air\",single crystal,300,3.51,31.25,17150,2511,1757,147.11,10.865,13.54,507,0.000799,15800,0.106\r\n10.1063/1.1562337,0.00217,152,0.43,Ca3Co4O9,\"flux (SrCl2), air\",single crystal,400,3.444,31.25,17150,2511,1757,147.11,10.865,13.54,460,0.00106,23100,0.13\r\n10.1063/1.1562337,0.00231,197,1.17,Ca3Co4O9,\"flux (SrCl2), air\",single crystal,700,3.15,31.25,17150,2511,1757,147.11,10.865,13.54,432,0.00168,38800,0.234\r\n10.1063/1.1562337,0.00227,245,2.64,Ca3Co4O9,\"flux (SrCl2), air\",single crystal,1000,2.837,31.25,17150,2511,1757,147.11,10.865,13.54,440,0.00264,60000,0.379\r\n10.1126/science.272.5266.1325,0.000993,68,0.14,Ce1Fe4Sb12,\"melted, vacuum\",polycrystalline,300,,107.33,4005000,7355,3146,762.3,22.421,34,1010,0.000469,4660,\r\n10.1126/science.272.5266.1326,0.00147,87,0.15,Ce1Fe3Co1Sb12,\"melted, vacuum\",polycrystalline,300,1.37,107.51,4000000,7367,3185,756.81,22.259,34,679,0.000509,7490,0.363\r\n10.1126/science.272.5266.1327,0.00274,104,0.12,Ce1Fe2.5Co1.5Sb12,\"melted, vacuum\",polycrystalline,300,,107.6,3997000,7373,3204,756.81,22.259,34,365,0.000397,10900,\r\n10.1126/science.272.5266.1328,0.00473,108,0.07,Ce1Fe2Co2Sb12,\"melted, vacuum\",polycrystalline,300,,107.69,3994000,7379,3223,747,21.971,34,211,0.000245,11600,\r\n10.1126/science.272.5266.1329,0.01,-87,0.02,Ce1Fe1Co3Sb12,\"melted, vacuum\",polycrystalline,300,,107.88,3988000,7391,3261,747,21.971,34,95.7,7.24E-05,7570,\r\n10.1126/science.272.5266.1330,0.061,16,0.000131,Ce1Fe1.5Co2.5Sb12,\"melted, vacuum\",polycrystalline,300,,107.78,3991000,7385,3242,747,21.971,34,16.4,4.38E-07,267,\r\n10.1126/science.272.5266.1331,0.00164,108,0.21,La1Fe3Co1Sb12,\"melted, vacuum\",polycrystalline,300,1.6,107.44,4003000,7366,3185,752.85,22.143,34,609,0.000715,11700,0.278\r\n10.1126/science.272.5266.1332,0.00106,87,0.29,Ce1Fe4Sb12,\"melted, vacuum\",polycrystalline,400,,107.33,4005000,7355,3146,762.3,22.421,34,947,0.000717,7570,\r\n10.1126/science.272.5266.1333,0.00163,108,0.29,Ce1Fe3Co1Sb12,\"melted, vacuum\",polycrystalline,400,,107.51,4000000,7367,3185,756.81,22.259,34,615,0.000713,11600,\r\n10.1126/science.272.5266.1334,0.00288,123,0.21,Ce1Fe2.5Co1.5Sb12,\"melted, vacuum\",polycrystalline,400,,107.6,3997000,7373,3204,756.81,22.259,34,347,0.000526,15100,\r\n10.1126/science.272.5266.1335,0.00481,135,0.15,Ce1Fe2Co2Sb12,\"melted, vacuum\",polycrystalline,400,,107.69,3994000,7379,3223,747,21.971,34,208,0.000376,18100,\r\n10.1126/science.272.5266.1336,0.00985,-102,0.04,Ce1Fe1Co3Sb12,\"melted, vacuum\",polycrystalline,400,,107.88,3988000,7391,3261,747,21.971,34,101,0.000106,10500,\r\n10.1126/science.272.5266.1337,0.045,12,0.000129,Ce1Fe1.5Co2.5Sb12,\"melted, vacuum\",polycrystalline,400,,107.78,3991000,7385,3242,747,21.971,34,22.4,3.23E-07,144,\r\n10.1126/science.272.5266.1338,0.00183,143,0.44,La1Fe3Co1Sb12,\"melted, vacuum\",polycrystalline,400,1.6,107.44,4003000,7366,3185,752.85,22.143,34,546,0.00111,20400,0.333\r\n10.1126/science.272.5266.1339,0.0013,129,0.89,Ce1Fe4Sb12,\"melted, vacuum\",polycrystalline,700,,107.33,4005000,7355,3146,762.3,22.421,34,768,0.00127,16600,\r\n10.1126/science.272.5266.1340,0.00202,150,0.78,Ce1Fe3Co1Sb12,\"melted, vacuum\",polycrystalline,700,,107.51,4000000,7367,3185,756.81,22.259,34,496,0.00111,22500,\r\n10.1126/science.272.5266.1341,0.00331,162,0.56,Ce1Fe2.5Co1.5Sb12,\"melted, vacuum\",polycrystalline,700,,107.6,3997000,7373,3204,756.81,22.259,34,302,0.000793,26200,\r\n10.1126/science.272.5266.1342,0.00488,164,0.39,Ce1Fe2Co2Sb12,\"melted, vacuum\",polycrystalline,700,,107.69,3994000,7379,3223,747,21.971,34,205,0.000551,26900,\r\n10.1126/science.272.5266.1343,0.00609,-141,0.23,Ce1Fe1Co3Sb12,\"melted, vacuum\",polycrystalline,700,,107.88,3988000,7391,3261,747,21.971,34,164,0.000326,19800,\r\n10.1126/science.272.5266.1344,0.012,-36,0.00742,Ce1Fe1.5Co2.5Sb12,\"melted, vacuum\",polycrystalline,700,,107.78,3991000,7385,3242,747,21.971,34,83.8,1.06E-05,1260,\r\n10.1126/science.272.5266.1345,0.00232,210,1.34,La1Fe3Co1Sb12,\"melted, vacuum\",polycrystalline,700,1.57,107.44,4003000,7366,3185,752.85,22.143,34,431,0.00191,44300,0.469\r\n10.1126/science.272.5266.1346,0.00174,157,1.41,Ce1Fe4Sb12,\"melted, vacuum\",polycrystalline,1000,,107.33,4005000,7355,3146,762.3,22.421,34,574,0.00141,24600,\r\n10.1126/science.272.5266.1347,0.0023,176,1.35,Ce1Fe3Co1Sb12,\"melted, vacuum\",polycrystalline,1000,,107.51,4000000,7367,3185,756.81,22.259,34,434,0.00135,31100,\r\n10.1126/science.272.5266.1348,0.00339,190,1.06,Ce1Fe2.5Co1.5Sb12,\"melted, vacuum\",polycrystalline,1000,,107.6,3997000,7373,3204,756.81,22.259,34,295,0.00106,36100,\r\n10.1126/science.272.5266.1349,0.00499,118,0.28,Ce1Fe2Co2Sb12,\"melted, vacuum\",polycrystalline,1000,,107.69,3994000,7379,3223,747,21.971,34,200,0.000278,13900,\r\n10.1126/science.272.5266.1350,0.00448,-138,0.42,Ce1Fe1Co3Sb12,\"melted, vacuum\",polycrystalline,1000,,107.88,3988000,7391,3261,747,21.971,34,223,0.000425,19000,\r\n10.1126/science.272.5266.1351,0.00397,-90,0.2,Ce1Fe1.5Co2.5Sb12,\"melted, vacuum\",polycrystalline,1000,,107.78,3991000,7385,3242,747,21.971,34,252,0.000203,8080,\r\n"
  },
  {
    "path": "dataset/Experimental thermoelectric properties 2013/MRL_all_raw_data.json",
    "content": "[{\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"50.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-463.0\", \"ZT\": \"0.000129\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.02\", \"Power Factor (W/(K\\u00b2m))\": \"4.29e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"214000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.046\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-202.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.98La0.02Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82210, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.0\", \"Scarcity (wt fraction/abundance)\": \"917.3\", \"HHI (production)\": \"1996.0\", \"HHI (reserves)\": \"1310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.74\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.387\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.7\", \"Power Factor (W/(K\\u00b2m))\": \"8.82e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-124.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.96La0.04Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82209, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.39\", \"Scarcity (wt fraction/abundance)\": \"1423.0\", \"HHI (production)\": \"2128.0\", \"HHI (reserves)\": \"1343.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.49\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.424\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"65.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.0001\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-104.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.94La0.06Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82208, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.79\", \"Scarcity (wt fraction/abundance)\": \"1915.0\", \"HHI (production)\": \"2255.0\", \"HHI (reserves)\": \"1376.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.24\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.462\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"82.2\", \"Power Factor (W/(K\\u00b2m))\": \"8.84e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.00997\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.92La0.08Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82207, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"2394.0\", \"HHI (production)\": \"2380.0\", \"HHI (reserves)\": \"1407.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.497\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"100.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.95e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6930.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"5.008\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-572.0\", \"ZT\": \"0.00196\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"Extrapolated from 325 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.2\", \"Power Factor (W/(K\\u00b2m))\": \"6.53e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"327000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.02\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-100.0\", \"ZT\": \"0.01\", \"formula\": \"Ca0.98Bi0.02Mn0.98Nb0.02O3\", \"comment\": \"Extrapolated from 325 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.513\", \"Average atomic mass (g/mol)\": \"29.43\", \"Scarcity (wt fraction/abundance)\": \"1672000.0\", \"HHI (production)\": \"2034.0\", \"HHI (reserves)\": \"1500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"49.2\", \"Power Factor (W/(K\\u00b2m))\": \"4.92e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.014\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.00886\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-91.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.96Bi0.04Mn0.96Nb0.04O3\", \"comment\": \"Extrapolated from 325 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.268\", \"Average atomic mass (g/mol)\": \"30.26\", \"Scarcity (wt fraction/abundance)\": \"3252000.0\", \"HHI (production)\": \"2198.0\", \"HHI (reserves)\": \"1711.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"113.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.38e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8310.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.036\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.00733\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-72.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.9Bi0.1Mn0.9Nb0.1O3\", \"comment\": \"Extrapolated from 325 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.74\", \"Scarcity (wt fraction/abundance)\": \"7513000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"2282.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"137.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.12e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5220.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/jmr.2011.140\", \"Electrical resistivity (\\u03a9cm)\": \"0.02\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-180.0\", \"ZT\": \"0.05\", \"formula\": \"Ca1Mn0.98Nb0.02O3\", \"comment\": \"\", \"synthesis\": \"Ultrasonic Spray Pyrolysis\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Populoh 2011\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.5\", \"Average atomic mass (g/mol)\": \"28.75\", \"Scarcity (wt fraction/abundance)\": \"1087.0\", \"HHI (production)\": \"1950.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"50.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000162\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"32400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.015\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.031\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-212.0\", \"ZT\": \"0.04\", \"formula\": \"Ca1Gd0.98Mn0.02O3\", \"comment\": \"Extrapolated from 323 K\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.66\", \"Scarcity (wt fraction/abundance)\": \"111100.0\", \"HHI (production)\": \"6744.0\", \"HHI (reserves)\": \"2336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"32.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000147\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-162.0\", \"ZT\": \"0.05\", \"formula\": \"Ca1Gd0.96Mn0.04O3\", \"comment\": \"Extrapolated from 323 K\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.787\", \"Average atomic mass (g/mol)\": \"48.25\", \"Scarcity (wt fraction/abundance)\": \"109800.0\", \"HHI (production)\": \"6685.0\", \"HHI (reserves)\": \"2323.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"67.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000177\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.028\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-104.0\", \"ZT\": \"0.02\", \"formula\": \"Ca1Gd0.94Mn0.06O3\", \"comment\": \"Extrapolated from 323 K\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.85\", \"Average atomic mass (g/mol)\": \"47.84\", \"Scarcity (wt fraction/abundance)\": \"108400.0\", \"HHI (production)\": \"6625.0\", \"HHI (reserves)\": \"2310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"68.8\", \"Power Factor (W/(K\\u00b2m))\": \"7.48e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.018\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00576\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-75.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9Tb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69824, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.484\", \"Average atomic mass (g/mol)\": \"30.98\", \"Scarcity (wt fraction/abundance)\": \"96250.0\", \"HHI (production)\": \"2591.0\", \"HHI (reserves)\": \"1460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.479\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"174.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.76e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.086\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00607\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-46.0\", \"ZT\": \"0.01\", \"formula\": \"Ca0.7Tb0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69826, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.17\", \"Average atomic mass (g/mol)\": \"35.73\", \"Scarcity (wt fraction/abundance)\": \"249700.0\", \"HHI (production)\": \"3759.0\", \"HHI (reserves)\": \"1755.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.15\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.658\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"165.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.53e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2140.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.056\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00669\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-72.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.9Ho0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160306, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.637\", \"Average atomic mass (g/mol)\": \"31.1\", \"Scarcity (wt fraction/abundance)\": \"85220.0\", \"HHI (production)\": \"2618.0\", \"HHI (reserves)\": \"1467.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.04\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.452\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"149.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.75e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5190.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.067\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00512\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-44.0\", \"ZT\": \"0.01\", \"formula\": \"Ca0.7Ho0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.144\", \"Average atomic mass (g/mol)\": \"36.09\", \"Scarcity (wt fraction/abundance)\": \"219600.0\", \"HHI (production)\": \"3816.0\", \"HHI (reserves)\": \"1769.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"195.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.73e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1910.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.067\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00437\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-71.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.489\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"229.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000114\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4970.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.112\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00763\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-42.0\", \"ZT\": \"0.00681\", \"formula\": \"Ca0.7Y0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #97601, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.793\", \"Average atomic mass (g/mol)\": \"31.53\", \"Scarcity (wt fraction/abundance)\": \"5816.0\", \"HHI (production)\": \"3058.0\", \"HHI (reserves)\": \"1490.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"219.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.992\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"131.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.27e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1730.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.054\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000434\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-26.0\", \"ZT\": \"0.05\", \"formula\": \"Ba1Pb1O3\", \"comment\": \"Extrapolated from 320 K\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.78\", \"Average atomic mass (g/mol)\": \"78.5\", \"Scarcity (wt fraction/abundance)\": \"44820.0\", \"HHI (production)\": \"2535.0\", \"HHI (reserves)\": \"1822.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2310.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000156\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"676.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.446\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000462\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-24.0\", \"ZT\": \"0.04\", \"formula\": \"Ba0.8Sr0.2Pb1O3\", \"comment\": \"Extrapolated from 320 K\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.746\", \"Average atomic mass (g/mol)\": \"76.52\", \"Scarcity (wt fraction/abundance)\": \"45940.0\", \"HHI (production)\": \"2579.0\", \"HHI (reserves)\": \"1839.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2160.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000129\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"598.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.577\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.00131\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-42.0\", \"ZT\": \"0.04\", \"formula\": \"Ba0.6Sr0.4Pb1O3\", \"comment\": \"Extrapolated from 320 K\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151609, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.306\", \"Average atomic mass (g/mol)\": \"74.53\", \"Scarcity (wt fraction/abundance)\": \"47120.0\", \"HHI (production)\": \"2625.0\", \"HHI (reserves)\": \"1856.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"301.96\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.098\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"766.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000135\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1760.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.243\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.00413\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.05\", \"formula\": \"Ba0.4Sr0.6Pb1O3\", \"comment\": \"Extrapolated from 320 K\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151609, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.295\", \"Average atomic mass (g/mol)\": \"72.54\", \"Scarcity (wt fraction/abundance)\": \"48360.0\", \"HHI (production)\": \"2674.0\", \"HHI (reserves)\": \"1874.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"301.96\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.098\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"242.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000166\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6850.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.077\"}, {\"doi\": \"10.1201/9781420049718.ch19\", \"Electrical resistivity (\\u03a9cm)\": \"0.00055\", \"Seebeck coefficient (\\u03bcCV/K)\": \"162.0\", \"ZT\": \"1.43\", \"formula\": \"Bi2Te3\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Scherrer 1995\", \"Structure\": \"ICSD #74348, 300K\", \"marker\": \"{'radius': 4.2944727273, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.468\", \"Average atomic mass (g/mol)\": \"160.15\", \"Scarcity (wt fraction/abundance)\": \"508700000.0\", \"HHI (production)\": \"4147.0\", \"HHI (reserves)\": \"5487.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"509.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.947\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1820.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00477\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.906\"}, {\"doi\": \"10.1201/9781420049718.ch19\", \"Electrical resistivity (\\u03a9cm)\": \"0.00045\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-174.0\", \"ZT\": \"2.02\", \"formula\": \"Bi2Te3\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Scherrer 1995\", \"Structure\": \"ICSD #74348, 300K\", \"marker\": \"{'radius': 6.0552, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"4.017\", \"Average atomic mass (g/mol)\": \"160.15\", \"Scarcity (wt fraction/abundance)\": \"508700000.0\", \"HHI (production)\": \"4147.0\", \"HHI (reserves)\": \"5487.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"509.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.947\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2220.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00673\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.405\"}, {\"doi\": \"10.1201/9781420049718.ch19\", \"Electrical resistivity (\\u03a9cm)\": \"0.00019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"38.0\", \"ZT\": \"0.23\", \"formula\": \"Sb2Te3\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Scherrer 1995\", \"Structure\": \"ICSD #2084, 300K\", \"marker\": \"{'radius': 0.684, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.378\", \"Average atomic mass (g/mol)\": \"125.26\", \"Scarcity (wt fraction/abundance)\": \"613100000.0\", \"HHI (production)\": \"4841.0\", \"HHI (reserves)\": \"4345.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"479.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.973\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5260.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00076\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1440.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.141\"}, {\"doi\": \"10.1201/9781420049718.ch19\", \"Electrical resistivity (\\u03a9cm)\": \"0.000122\", \"Seebeck coefficient (\\u03bcCV/K)\": \"63.0\", \"ZT\": \"0.98\", \"formula\": \"Sb2Te3\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Scherrer 1995\", \"Structure\": \"ICSD #2084, 300K\", \"marker\": \"{'radius': 2.9279508197, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"5.205\", \"Average atomic mass (g/mol)\": \"125.26\", \"Scarcity (wt fraction/abundance)\": \"613100000.0\", \"HHI (production)\": \"4841.0\", \"HHI (reserves)\": \"4345.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"479.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.973\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"8200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00325\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3970.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.153\"}, {\"doi\": \"10.1201/9781420049718.ch22\", \"Electrical resistivity (\\u03a9cm)\": \"0.000694\", \"Seebeck coefficient (\\u03bcCV/K)\": \"79.0\", \"ZT\": \"0.27\", \"formula\": \"Ag0.15Sb0.15Te1.15Ge0.85\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Skrabek 1995\", \"Structure\": \"ICSD #2084, 300K\", \"marker\": \"{'radius': 0.802326846, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.499\", \"Average atomic mass (g/mol)\": \"105.62\", \"Scarcity (wt fraction/abundance)\": \"605500000.0\", \"HHI (production)\": \"3762.0\", \"HHI (reserves)\": \"3810.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"479.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.973\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1440.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000891\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6190.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.704\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00598\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-280.0\", \"ZT\": \"0.39\", \"formula\": \"In0.05Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 1.1795744172, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.087\", \"Average atomic mass (g/mol)\": \"106.08\", \"Scarcity (wt fraction/abundance)\": \"4312000.0\", \"HHI (production)\": \"7219.0\", \"HHI (reserves)\": \"3308.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"739.646\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.042\", \"Atoms per unit cell\": \"32.1\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"167.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00131\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"78300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.059\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00292\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-257.0\", \"ZT\": \"0.68\", \"formula\": \"In0.1Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 2.0403363477, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.188\", \"Average atomic mass (g/mol)\": \"106.11\", \"Scarcity (wt fraction/abundance)\": \"4314000.0\", \"HHI (production)\": \"7205.0\", \"HHI (reserves)\": \"3304.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"741.144\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.017\", \"Atoms per unit cell\": \"32.2\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"342.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00227\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"66200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.115\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00187\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-247.0\", \"ZT\": \"0.97\", \"formula\": \"In0.15Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 2.9238334723, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.299\", \"Average atomic mass (g/mol)\": \"106.13\", \"Scarcity (wt fraction/abundance)\": \"4316000.0\", \"HHI (production)\": \"7192.0\", \"HHI (reserves)\": \"3300.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"741.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.953\", \"Atoms per unit cell\": \"32.3\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"534.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00325\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"60800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.17\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00149\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-222.0\", \"ZT\": \"0.99\", \"formula\": \"In0.2Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 2.9767010156, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.476\", \"Average atomic mass (g/mol)\": \"106.16\", \"Scarcity (wt fraction/abundance)\": \"4318000.0\", \"HHI (production)\": \"7180.0\", \"HHI (reserves)\": \"3295.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.742\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.924\", \"Atoms per unit cell\": \"32.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"670.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00331\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"49300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.198\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00114\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-217.0\", \"ZT\": \"1.24\", \"formula\": \"In0.25Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 3.7229848348, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.559\", \"Average atomic mass (g/mol)\": \"106.19\", \"Scarcity (wt fraction/abundance)\": \"4320000.0\", \"HHI (production)\": \"7167.0\", \"HHI (reserves)\": \"3291.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.89\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.858\", \"Atoms per unit cell\": \"32.5\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"878.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00414\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"47100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.251\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00151\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-212.0\", \"ZT\": \"0.89\", \"formula\": \"In0.3Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 2.6738678986, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.688\", \"Average atomic mass (g/mol)\": \"106.21\", \"Scarcity (wt fraction/abundance)\": \"4322000.0\", \"HHI (production)\": \"7154.0\", \"HHI (reserves)\": \"3287.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.89\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.788\", \"Atoms per unit cell\": \"32.6\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"662.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00297\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.18\"}, {\"doi\": \"10.1557/jmr.2011.163\", \"Electrical resistivity (\\u03a9cm)\": \"0.00113\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-192.0\", \"ZT\": \"0.98\", \"formula\": \"In0.2Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Biswas 2011\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 2.9312482501, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.57\", \"Average atomic mass (g/mol)\": \"106.16\", \"Scarcity (wt fraction/abundance)\": \"4318000.0\", \"HHI (production)\": \"7180.0\", \"HHI (reserves)\": \"3295.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.742\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.924\", \"Atoms per unit cell\": \"32.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"882.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00326\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.251\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.000369\", \"Seebeck coefficient (\\u03bcCV/K)\": \"62.0\", \"ZT\": \"0.32\", \"formula\": \"Na0.02Pb1Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 0.9501621685, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.996\", \"Average atomic mass (g/mol)\": \"165.97\", \"Scarcity (wt fraction/abundance)\": \"380700000.0\", \"HHI (production)\": \"2781.0\", \"HHI (reserves)\": \"2979.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2710.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00106\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3890.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.497\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.000413\", \"Seebeck coefficient (\\u03bcCV/K)\": \"51.0\", \"ZT\": \"0.19\", \"formula\": \"Na0.02Pb1Te0.85Se0.15\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 0.5654410232, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.014\", \"Average atomic mass (g/mol)\": \"162.36\", \"Scarcity (wt fraction/abundance)\": \"331500000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2827.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2420.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000628\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.588\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.000512\", \"Seebeck coefficient (\\u03bcCV/K)\": \"59.0\", \"ZT\": \"0.2\", \"formula\": \"Na0.02Pb1Te0.75Se0.25\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 0.6074784906, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.696\", \"Average atomic mass (g/mol)\": \"159.95\", \"Scarcity (wt fraction/abundance)\": \"297500000.0\", \"HHI (production)\": \"2736.0\", \"HHI (reserves)\": \"2721.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1950.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000675\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3460.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.53\"}, {\"doi\": \"10.1126/science.1159725\", \"Electrical resistivity (\\u03a9cm)\": \"0.00274\", \"Seebeck coefficient (\\u03bcCV/K)\": \"140.0\", \"ZT\": \"0.22\", \"formula\": \"Tl0.01Pb0.99Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Heremans 2008\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 0.646908351, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.942\", \"Average atomic mass (g/mol)\": \"167.39\", \"Scarcity (wt fraction/abundance)\": \"381200000.0\", \"HHI (production)\": \"2806.0\", \"HHI (reserves)\": \"3012.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"365.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000719\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.137\"}, {\"doi\": \"10.1126/science.1159725\", \"Electrical resistivity (\\u03a9cm)\": \"0.00239\", \"Seebeck coefficient (\\u03bcCV/K)\": \"136.0\", \"ZT\": \"0.23\", \"formula\": \"Tl0.02Pb0.98Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Heremans 2008\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 0.6970952493, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.168\", \"Average atomic mass (g/mol)\": \"167.37\", \"Scarcity (wt fraction/abundance)\": \"381300000.0\", \"HHI (production)\": \"2829.0\", \"HHI (reserves)\": \"3041.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"418.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000775\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.141\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00182\", \"Seebeck coefficient (\\u03bcCV/K)\": \"169.0\", \"ZT\": \"0.47\", \"formula\": \"Si0.9Ge0.1\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"300\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.4108068057, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.54\", \"Scarcity (wt fraction/abundance)\": \"153900.0\", \"HHI (production)\": \"4833.0\", \"HHI (reserves)\": \"1200.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"549.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00157\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.0015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"137.0\", \"ZT\": \"0.38\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"300\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.1299063545, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"669.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00126\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.00133\", \"Seebeck coefficient (\\u03bcCV/K)\": \"128.0\", \"ZT\": \"0.37\", \"formula\": \"Si0.79936Ge0.19984B0.0008\", \"comment\": \"Kappa extrapolated from 375 K\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.0994896502, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"4.34\", \"Average atomic mass (g/mol)\": \"36.98\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4927.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"750.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00122\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.126\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.00117\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-123.0\", \"ZT\": \"0.39\", \"formula\": \"Si0.7956Ge0.1989P0.0055\", \"comment\": \"Kappa extrapolated from 375 K\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.1601100268, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"4.139\", \"Average atomic mass (g/mol)\": \"36.96\", \"Scarcity (wt fraction/abundance)\": \"269600.0\", \"HHI (production)\": \"4914.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"855.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00129\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.151\"}, {\"doi\": \"10.1063/1.4765358\", \"Electrical resistivity (\\u03a9cm)\": \"0.0075\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-200.0\", \"ZT\": \"0.16\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"Magnetic levitation induction furnace\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Douglas 2012\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 0.48, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.72\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"133.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000533\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.013\"}, {\"doi\": \"10.1063/1.1502190\", \"Electrical resistivity (\\u03a9cm)\": \"0.00212\", \"Seebeck coefficient (\\u03bcCV/K)\": \"109.0\", \"ZT\": \"0.17\", \"formula\": \"Bi2Sr2Co2O8\", \"comment\": \"\", \"synthesis\": \"Solid state reaction + extra\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Funahashi 2002\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 0.5023664453, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.185\", \"Average atomic mass (g/mol)\": \"59.93\", \"Scarcity (wt fraction/abundance)\": \"29310000.0\", \"HHI (production)\": \"4016.0\", \"HHI (reserves)\": \"4061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.53\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.59\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"471.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000558\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.158\"}, {\"doi\": \"10.1021/cm970397e\", \"Electrical resistivity (\\u03a9cm)\": \"0.032\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-196.0\", \"ZT\": \"0.04\", \"formula\": \"K2Bi8Se13\", \"comment\": \"\", \"synthesis\": \"Solid state reaction + extra\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Chung 1997\", \"Structure\": \"ICSD #84268, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.285\", \"Average atomic mass (g/mol)\": \"120.72\", \"Scarcity (wt fraction/abundance)\": \"42810000.0\", \"HHI (production)\": \"4060.0\", \"HHI (reserves)\": \"4518.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1357.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.518\", \"Atoms per unit cell\": \"46.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"30.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000119\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.018\"}, {\"doi\": \"10.1021/cm970397e\", \"Electrical resistivity (\\u03a9cm)\": \"0.00416\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-220.0\", \"ZT\": \"0.35\", \"formula\": \"K2Bi8Se13\", \"comment\": \"\", \"synthesis\": \"Flux (Bi self-flux)\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Chung 1997\", \"Structure\": \"ICSD #84268, 298K\", \"marker\": \"{'radius': 1.0436471736, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"120.72\", \"Scarcity (wt fraction/abundance)\": \"42810000.0\", \"HHI (production)\": \"4060.0\", \"HHI (reserves)\": \"4518.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1357.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.518\", \"Atoms per unit cell\": \"46.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"240.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00116\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.39.L1127\", \"Electrical resistivity (\\u03a9cm)\": \"0.00147\", \"Seebeck coefficient (\\u03bcCV/K)\": \"135.0\", \"ZT\": \"0.37\", \"formula\": \"Ca2Co2O5\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Funahashi 2000\", \"Structure\": \"ICSD #55458, 300K\", \"marker\": \"{'radius': 1.1186376111, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.3\", \"Average atomic mass (g/mol)\": \"30.89\", \"Scarcity (wt fraction/abundance)\": \"15420.0\", \"HHI (production)\": \"2551.0\", \"HHI (reserves)\": \"1702.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"236.38\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.883\", \"Atoms per unit cell\": \"21.72\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"681.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00124\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.217\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00124\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-28.0\", \"ZT\": \"0.02\", \"formula\": \"W1O2.9\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24736, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.083\", \"Average atomic mass (g/mol)\": \"59.04\", \"Scarcity (wt fraction/abundance)\": \"679600.0\", \"HHI (production)\": \"5675.0\", \"HHI (reserves)\": \"3532.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1066.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.328\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"808.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.42e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"796.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.192\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"6.46e-05\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-26.0\", \"ZT\": \"0.31\", \"formula\": \"W1O2.722\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24731, 300K\", \"marker\": \"{'radius': 0.9230585609, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"8.177\", \"Average atomic mass (g/mol)\": \"61.09\", \"Scarcity (wt fraction/abundance)\": \"688100.0\", \"HHI (production)\": \"5740.0\", \"HHI (reserves)\": \"3570.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"883.29\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.268\", \"Atoms per unit cell\": \"72.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"15500.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00103\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"662.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.386\"}, {\"doi\": \"10.1103/PhysRevB.59.192\", \"Electrical resistivity (\\u03a9cm)\": \"0.073\", \"Seebeck coefficient (\\u03bcCV/K)\": \"218.0\", \"ZT\": \"0.02\", \"formula\": \"La2Cu1O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Choi 1999\", \"Structure\": \"ICSD #83486, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.91\", \"Scarcity (wt fraction/abundance)\": \"21230.0\", \"HHI (production)\": \"6820.0\", \"HHI (reserves)\": \"2462.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"338.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.074\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"13.8\", \"Power Factor (W/(K\\u00b2m))\": \"6.52e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"47300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2012.03.013\", \"Electrical resistivity (\\u03a9cm)\": \"0.0032\", \"Seebeck coefficient (\\u03bcCV/K)\": \"130.0\", \"ZT\": \"0.16\", \"formula\": \"La1.61Sr0.39Cu0.94Ti0.06O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2012\", \"Structure\": \"ICSD #184669, 293K\", \"marker\": \"{'radius': 0.4753125, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"54.92\", \"Scarcity (wt fraction/abundance)\": \"18610.0\", \"HHI (production)\": \"6221.0\", \"HHI (reserves)\": \"2419.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"188.19\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.442\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"312.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000528\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2012.03.013\", \"Electrical resistivity (\\u03a9cm)\": \"12.6\", \"Seebeck coefficient (\\u03bcCV/K)\": \"200.0\", \"ZT\": \"9.52e-05\", \"formula\": \"La1.85Sr0.15Cu0.94Ti0.06O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2012\", \"Structure\": \"ICSD #184665, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.67\", \"Scarcity (wt fraction/abundance)\": \"20190.0\", \"HHI (production)\": \"6603.0\", \"HHI (reserves)\": \"2448.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.549\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.079\", \"Power Factor (W/(K\\u00b2m))\": \"3.17e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2012.03.013\", \"Electrical resistivity (\\u03a9cm)\": \"0.0039\", \"Seebeck coefficient (\\u03bcCV/K)\": \"20.0\", \"ZT\": \"0.00308\", \"formula\": \"La1.73Sr0.27Cu0.94Ti0.06O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2012\", \"Structure\": \"ICSD #184666, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.79\", \"Scarcity (wt fraction/abundance)\": \"19410.0\", \"HHI (production)\": \"6415.0\", \"HHI (reserves)\": \"2433.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"188.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.469\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"256.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.03e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2012.03.013\", \"Electrical resistivity (\\u03a9cm)\": \"0.0035\", \"Seebeck coefficient (\\u03bcCV/K)\": \"5.0\", \"ZT\": \"0.000214\", \"formula\": \"La1.69Sr0.31Cu0.94Ti0.06O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2012\", \"Structure\": \"ICSD #184667, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.5\", \"Scarcity (wt fraction/abundance)\": \"19150.0\", \"HHI (production)\": \"6351.0\", \"HHI (reserves)\": \"2429.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"188.45\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.461\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"286.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.14e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2012.03.013\", \"Electrical resistivity (\\u03a9cm)\": \"0.0032\", \"Seebeck coefficient (\\u03bcCV/K)\": \"6.0\", \"ZT\": \"0.000372\", \"formula\": \"La1.67Sr0.34Cu0.94Ti0.06O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2012\", \"Structure\": \"ICSD #184668, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.4\", \"Scarcity (wt fraction/abundance)\": \"18980.0\", \"HHI (production)\": \"6314.0\", \"HHI (reserves)\": \"2427.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"188.41\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.458\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"312.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.24e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"39.7\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00818\", \"Seebeck coefficient (\\u03bcCV/K)\": \"150.0\", \"ZT\": \"0.08\", \"formula\": \"La1.95Sr0.05Cu1O4\", \"comment\": \"Seebeck from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78632, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.54\", \"Scarcity (wt fraction/abundance)\": \"20920.0\", \"HHI (production)\": \"6746.0\", \"HHI (reserves)\": \"2457.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.25\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.58\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"122.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000275\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.0028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"55.0\", \"ZT\": \"0.03\", \"formula\": \"La1.9Sr0.1Cu1O4\", \"comment\": \"Seebeck from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78240, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.17\", \"Scarcity (wt fraction/abundance)\": \"20610.0\", \"HHI (production)\": \"6670.0\", \"HHI (reserves)\": \"2451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"378.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.514\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"357.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000107\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2990.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00113\", \"Seebeck coefficient (\\u03bcCV/K)\": \"25.0\", \"ZT\": \"0.02\", \"formula\": \"La1.85Sr0.15Cu1O4\", \"comment\": \"Seebeck from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.81\", \"Scarcity (wt fraction/abundance)\": \"20290.0\", \"HHI (production)\": \"6594.0\", \"HHI (reserves)\": \"2445.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"887.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.55e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"625.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.000471\", \"Seebeck coefficient (\\u03bcCV/K)\": \"0.0\", \"ZT\": \"1.59e-05\", \"formula\": \"La1.725Sr0.28Cu1O4\", \"comment\": \"Seebeck from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.92\", \"Scarcity (wt fraction/abundance)\": \"19470.0\", \"HHI (production)\": \"6396.0\", \"HHI (reserves)\": \"2431.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2120.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.3e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"0.25\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"215.0\", \"ZT\": \"0.1\", \"formula\": \"Tl1Cr5Se8\", \"comment\": \"Takahashi2012EMRS\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nunna 2012\", \"Structure\": \"ICSD #37123, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"78.29\", \"Scarcity (wt fraction/abundance)\": \"11800000.0\", \"HHI (production)\": \"3230.0\", \"HHI (reserves)\": \"3274.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"581.29\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.76\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"71.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.00033\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"46200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c2jm16297k\", \"Electrical resistivity (\\u03a9cm)\": \"1890.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-175.0\", \"ZT\": \"4.87e-07\", \"formula\": \"Li1Mn2O4\", \"comment\": \"Extrapolated from 370 K\", \"synthesis\": \"Solid state reaction (oxalates)\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sparks 2012\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00053\", \"Power Factor (W/(K\\u00b2m))\": \"1.62e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.107\", \"Seebeck coefficient (\\u03bcCV/K)\": \"277.0\", \"ZT\": \"0.02\", \"formula\": \"Cu1Fe0.9Cr0.1O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #31918, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.75\", \"Scarcity (wt fraction/abundance)\": \"6756.0\", \"HHI (production)\": \"1683.0\", \"HHI (reserves)\": \"1344.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"136.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.412\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.339\", \"Power Factor (W/(K\\u00b2m))\": \"7.17e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"76800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.0018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"98.0\", \"ZT\": \"0.16\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.4782765394, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"557.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000531\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9540.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.197\", \"Seebeck coefficient (\\u03bcCV/K)\": \"300.0\", \"ZT\": \"0.01\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5.085\", \"Power Factor (W/(K\\u00b2m))\": \"4.58e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"90000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"1400.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"98.0\", \"ZT\": \"2.05e-07\", \"formula\": \"W1O3\", \"comment\": \"Extrapolated from 370 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.96\", \"Scarcity (wt fraction/abundance)\": \"674900.0\", \"HHI (production)\": \"5639.0\", \"HHI (reserves)\": \"3511.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.000713\", \"Power Factor (W/(K\\u00b2m))\": \"6.83e-10\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9590.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"1250.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"93.0\", \"ZT\": \"2.06e-07\", \"formula\": \"W0.99O2.97Co0.02O0.03\", \"comment\": \"Extrapolated from 370 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.65\", \"Scarcity (wt fraction/abundance)\": \"670200.0\", \"HHI (production)\": \"5615.0\", \"HHI (reserves)\": \"3500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.000802\", \"Power Factor (W/(K\\u00b2m))\": \"6.88e-10\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8570.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"114.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"103.0\", \"ZT\": \"2.79e-06\", \"formula\": \"W0.95O2.95Co0.1O0.15\", \"comment\": \"Extrapolated from 370 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.45\", \"Scarcity (wt fraction/abundance)\": \"646800.0\", \"HHI (production)\": \"5484.0\", \"HHI (reserves)\": \"3437.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00873\", \"Power Factor (W/(K\\u00b2m))\": \"9.31e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"561.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"104.0\", \"ZT\": \"5.77e-07\", \"formula\": \"W0.9O2.7Co0.2O0.3\", \"comment\": \"Extrapolated from 370 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"54.94\", \"Scarcity (wt fraction/abundance)\": \"627100.0\", \"HHI (production)\": \"5394.0\", \"HHI (reserves)\": \"3402.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00178\", \"Power Factor (W/(K\\u00b2m))\": \"1.92e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.303\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-651.0\", \"ZT\": \"0.04\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.562\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.305\", \"Power Factor (W/(K\\u00b2m))\": \"0.00014\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"424000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000679\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00919\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-109.0\", \"ZT\": \"0.04\", \"formula\": \"Ca1Yb0.05Mn0.95O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.49\", \"Average atomic mass (g/mol)\": \"29.78\", \"Scarcity (wt fraction/abundance)\": \"19730.0\", \"HHI (production)\": \"2309.0\", \"HHI (reserves)\": \"1374.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"109.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00013\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.053\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.0039\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-53.0\", \"ZT\": \"0.02\", \"formula\": \"Ca1Yb0.1Mn0.9O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.725\", \"Average atomic mass (g/mol)\": \"30.96\", \"Scarcity (wt fraction/abundance)\": \"37590.0\", \"HHI (production)\": \"2722.0\", \"HHI (reserves)\": \"1465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"256.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.15e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2790.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.109\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00336\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-38.0\", \"ZT\": \"0.01\", \"formula\": \"Ca1Yb0.15Mn0.85O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.645\", \"Average atomic mass (g/mol)\": \"32.15\", \"Scarcity (wt fraction/abundance)\": \"54140.0\", \"HHI (production)\": \"3105.0\", \"HHI (reserves)\": \"1549.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"297.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.35e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1460.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.132\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-9.0\", \"ZT\": \"0.000163\", \"formula\": \"Ca1Yb0.4Mn0.6O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"121500.0\", \"HHI (production)\": \"4663.0\", \"HHI (reserves)\": \"1891.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"65.7\", \"Power Factor (W/(K\\u00b2m))\": \"5.45e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"82.9\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-156.0\", \"ZT\": \"0.05\", \"formula\": \"In2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"9.67\", \"Average atomic mass (g/mol)\": \"55.53\", \"Scarcity (wt fraction/abundance)\": \"4035000.0\", \"HHI (production)\": \"2843.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"74.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00018\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"24400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0056\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00211\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.11\", \"formula\": \"In1.998Ge0.002O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.335254304, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"9.156\", \"Average atomic mass (g/mol)\": \"55.51\", \"Scarcity (wt fraction/abundance)\": \"4032000.0\", \"HHI (production)\": \"2844.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"475.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000373\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7840.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.038\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.000837\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-50.0\", \"ZT\": \"0.09\", \"formula\": \"In1.994Ge0.006O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"9.715\", \"Average atomic mass (g/mol)\": \"55.48\", \"Scarcity (wt fraction/abundance)\": \"4027000.0\", \"HHI (production)\": \"2846.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000304\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2550.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.09\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.000723\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-47.0\", \"ZT\": \"0.09\", \"formula\": \"In1.985Ge0.015O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"9.419\", \"Average atomic mass (g/mol)\": \"55.4\", \"Scarcity (wt fraction/abundance)\": \"4016000.0\", \"HHI (production)\": \"2850.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1380.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000302\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2190.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.107\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.000896\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-51.0\", \"ZT\": \"0.09\", \"formula\": \"In1.94Ge0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"8.868\", \"Average atomic mass (g/mol)\": \"55.02\", \"Scarcity (wt fraction/abundance)\": \"3961000.0\", \"HHI (production)\": \"2869.0\", \"HHI (reserves)\": \"1737.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1120.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000288\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2580.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.092\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00132\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-53.0\", \"ZT\": \"0.06\", \"formula\": \"In1.9Ge0.1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"6.847\", \"Average atomic mass (g/mol)\": \"54.68\", \"Scarcity (wt fraction/abundance)\": \"3910000.0\", \"HHI (production)\": \"2887.0\", \"HHI (reserves)\": \"1734.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"757.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000215\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2840.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.081\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00287\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-52.0\", \"ZT\": \"0.03\", \"formula\": \"In1.8Ge0.2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.238\", \"Average atomic mass (g/mol)\": \"53.84\", \"Scarcity (wt fraction/abundance)\": \"3782000.0\", \"HHI (production)\": \"2932.0\", \"HHI (reserves)\": \"1727.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"348.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.53e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2740.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.079\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"7.718\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-390.0\", \"ZT\": \"0.000591\", \"formula\": \"La1Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.879\", \"Average atomic mass (g/mol)\": \"49.17\", \"Scarcity (wt fraction/abundance)\": \"24200.0\", \"HHI (production)\": \"6184.0\", \"HHI (reserves)\": \"2502.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.13\", \"Power Factor (W/(K\\u00b2m))\": \"1.97e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"152000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"5.05e-05\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.157\", \"Seebeck coefficient (\\u03bcCV/K)\": \"395.0\", \"ZT\": \"0.03\", \"formula\": \"La0.99Sr0.01Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.807\", \"Average atomic mass (g/mol)\": \"49.06\", \"Scarcity (wt fraction/abundance)\": \"24100.0\", \"HHI (production)\": \"6158.0\", \"HHI (reserves)\": \"2500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"6.368\", \"Power Factor (W/(K\\u00b2m))\": \"9.94e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"156000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00258\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.069\", \"Seebeck coefficient (\\u03bcCV/K)\": \"330.0\", \"ZT\": \"0.05\", \"formula\": \"La0.98Sr0.02Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.8\", \"Average atomic mass (g/mol)\": \"48.96\", \"Scarcity (wt fraction/abundance)\": \"24010.0\", \"HHI (production)\": \"6132.0\", \"HHI (reserves)\": \"2499.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"14.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000157\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"109000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00588\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"215.0\", \"ZT\": \"0.09\", \"formula\": \"La0.95Sr0.05Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247230, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.8\", \"Average atomic mass (g/mol)\": \"48.65\", \"Scarcity (wt fraction/abundance)\": \"23720.0\", \"HHI (production)\": \"6053.0\", \"HHI (reserves)\": \"2493.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.147\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"62.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000289\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"46100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.025\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000468\", \"Seebeck coefficient (\\u03bcCV/K)\": \"21.0\", \"ZT\": \"0.03\", \"formula\": \"La0.8Sr0.2Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247232, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"3.696\", \"Average atomic mass (g/mol)\": \"47.12\", \"Scarcity (wt fraction/abundance)\": \"22220.0\", \"HHI (production)\": \"5646.0\", \"HHI (reserves)\": \"2465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"224.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.21\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2140.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.72e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"455.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.423\"}, {\"doi\": \"10.1021/cm060261t\", \"Electrical resistivity (\\u03a9cm)\": \"0.00204\", \"Seebeck coefficient (\\u03bcCV/K)\": \"56.0\", \"ZT\": \"0.05\", \"formula\": \"Yb14Mn1Sb11\", \"comment\": \"\", \"synthesis\": \"flux (Sn), Ar\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Brown 2006\", \"Structure\": \"ICSD #85638, 143K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.84\", \"Average atomic mass (g/mol)\": \"146.81\", \"Scarcity (wt fraction/abundance)\": \"1966000.0\", \"HHI (production)\": \"8812.0\", \"HHI (reserves)\": \"3211.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"6058.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.129\", \"Atoms per unit cell\": \"208.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"490.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000156\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3190.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.427\"}, {\"doi\": \"10.1016/S0022-3697(96)00228-4\", \"Electrical resistivity (\\u03a9cm)\": \"0.00211\", \"Seebeck coefficient (\\u03bcCV/K)\": \"111.0\", \"ZT\": \"0.18\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"melted, inert\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Caillat 1997\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 0.5250012083, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.01\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"475.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000583\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.344\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.00391\", \"Seebeck coefficient (\\u03bcCV/K)\": \"126.0\", \"ZT\": \"0.12\", \"formula\": \"Ce1Fe2Co2Sb12\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.3654322251, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.69\", \"Scarcity (wt fraction/abundance)\": \"3994000.0\", \"HHI (production)\": \"7379.0\", \"HHI (reserves)\": \"3223.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"256.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000406\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.00103\", \"Seebeck coefficient (\\u03bcCV/K)\": \"101.0\", \"ZT\": \"0.3\", \"formula\": \"Ce1Fe3Co1Sb12\", \"comment\": \"*kappa extrapolated from 400 K\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.8913495146, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.91\", \"Average atomic mass (g/mol)\": \"107.51\", \"Scarcity (wt fraction/abundance)\": \"4000000.0\", \"HHI (production)\": \"7367.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"971.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00099\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.372\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.000893\", \"Seebeck coefficient (\\u03bcCV/K)\": \"87.0\", \"ZT\": \"0.26\", \"formula\": \"Ce1Fe3.5Co0.5Sb12\", \"comment\": \"*kappa extrapolated from 400 K\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.7663444569, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.4\", \"Average atomic mass (g/mol)\": \"107.42\", \"Scarcity (wt fraction/abundance)\": \"4002000.0\", \"HHI (production)\": \"7361.0\", \"HHI (reserves)\": \"3165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1120.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000851\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.342\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.000771\", \"Seebeck coefficient (\\u03bcCV/K)\": \"58.0\", \"ZT\": \"0.13\", \"formula\": \"Ce1Fe4Sb12\", \"comment\": \"*kappa extrapolated from 400 K\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.3953976654, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.55\", \"Average atomic mass (g/mol)\": \"107.33\", \"Scarcity (wt fraction/abundance)\": \"4005000.0\", \"HHI (production)\": \"7355.0\", \"HHI (reserves)\": \"3146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"762.5\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.426\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1300.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000439\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3390.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.613\"}, {\"doi\": \"10.1021/cm200581k\", \"Electrical resistivity (\\u03a9cm)\": \"0.045\", \"Seebeck coefficient (\\u03bcCV/K)\": \"279.0\", \"ZT\": \"0.05\", \"formula\": \"Ag1Cr1Se2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, sealed\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Gascoin 2011\", \"Structure\": \"ICSD #68423, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.956\", \"Average atomic mass (g/mol)\": \"79.45\", \"Scarcity (wt fraction/abundance)\": \"14290000.0\", \"HHI (production)\": \"2031.0\", \"HHI (reserves)\": \"2077.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"248.9\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.742\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"22.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000175\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"78000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.017\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.051\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-132.0\", \"ZT\": \"0.01\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"19.6\", \"Power Factor (W/(K\\u00b2m))\": \"3.41e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-115.0\", \"ZT\": \"0.03\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"66.2\", \"Power Factor (W/(K\\u00b2m))\": \"8.82e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-114.0\", \"ZT\": \"0.04\", \"formula\": \"Zn0.9925Al0.0075O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"10740.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1618.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"97.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000126\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00678\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-111.0\", \"ZT\": \"0.05\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"148.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000182\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.021\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-145.0\", \"ZT\": \"0.03\", \"formula\": \"Zn0.97Al0.03O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.11\", \"Scarcity (wt fraction/abundance)\": \"10610.0\", \"HHI (production)\": \"1360.0\", \"HHI (reserves)\": \"1608.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.7\", \"Power Factor (W/(K\\u00b2m))\": \"9.81e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-81.0\", \"ZT\": \"0.00756\", \"formula\": \"Sr1Mn0.98Mo0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.28\", \"Scarcity (wt fraction/abundance)\": \"10260.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"38.8\", \"Power Factor (W/(K\\u00b2m))\": \"2.52e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6490.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-110.0\", \"ZT\": \"0.02\", \"formula\": \"Sr1Mn0.96Mo0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.44\", \"Scarcity (wt fraction/abundance)\": \"18890.0\", \"HHI (production)\": \"2515.0\", \"HHI (reserves)\": \"2089.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"64.9\", \"Power Factor (W/(K\\u00b2m))\": \"7.9e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.60.14057\", \"Electrical resistivity (\\u03a9cm)\": \"0.249\", \"Seebeck coefficient (\\u03bcCV/K)\": \"69.0\", \"ZT\": \"0.000581\", \"formula\": \"Sm1.7Ca0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Hejtmanek 1999\", \"Structure\": \"ICSD #85652, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.1\", \"Average atomic mass (g/mol)\": \"61.76\", \"Scarcity (wt fraction/abundance)\": \"105900.0\", \"HHI (production)\": \"6963.0\", \"HHI (reserves)\": \"2537.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"219.13\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.956\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.018\", \"Power Factor (W/(K\\u00b2m))\": \"1.94e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4820.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00267\"}, {\"doi\": \"10.1103/PhysRevB.60.14057\", \"Electrical resistivity (\\u03a9cm)\": \"0.00955\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-33.0\", \"ZT\": \"0.00333\", \"formula\": \"Sm0.5Ca0.5Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Hejtmanek 1999\", \"Structure\": \"ICSD #85652, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.9\", \"Average atomic mass (g/mol)\": \"39.63\", \"Scarcity (wt fraction/abundance)\": \"58430.0\", \"HHI (production)\": \"4548.0\", \"HHI (reserves)\": \"1956.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"219.13\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.956\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"105.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.11e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1060.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.04\"}, {\"doi\": \"10.1103/PhysRevB.60.14057\", \"Electrical resistivity (\\u03a9cm)\": \"0.029\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-358.0\", \"ZT\": \"0.13\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Hejtmanek 1999\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.4032592913, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"16.23\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"35.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000448\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"128000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00158\"}, {\"doi\": \"10.1016/j.jallcom.2004.02.061\", \"Electrical resistivity (\\u03a9cm)\": \"0.00105\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-133.0\", \"ZT\": \"0.51\", \"formula\": \"Zr1Ni1.98Cu0.02Sn1\", \"comment\": \"*kappa extrapolated from 375 K\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Katsumyama 2004\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 1.5162, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.98\", \"Average atomic mass (g/mol)\": \"81.85\", \"Scarcity (wt fraction/abundance)\": \"165700.0\", \"HHI (production)\": \"2246.0\", \"HHI (reserves)\": \"1848.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"952.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00168\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.087\"}, {\"doi\": \"10.1016/j.jallcom.2004.02.061\", \"Electrical resistivity (\\u03a9cm)\": \"0.00876\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-95.0\", \"ZT\": \"0.03\", \"formula\": \"Zr1Ni0.76Co0.004Cu0.2Sn1\", \"comment\": \"\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Katsumyama 2004\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.02\", \"Average atomic mass (g/mol)\": \"90.24\", \"Scarcity (wt fraction/abundance)\": \"201300.0\", \"HHI (production)\": \"2555.0\", \"HHI (reserves)\": \"1934.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"114.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000103\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9020.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.014\"}, {\"doi\": \"10.1016/j.jallcom.2006.02.075\", \"Electrical resistivity (\\u03a9cm)\": \"0.000598\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-113.0\", \"ZT\": \"0.64\", \"formula\": \"Zr1Ni1Sn0.98Sb0.02\", \"comment\": \"*extrapolated from 350 K\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Katsumyama 2007\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 1.9217558528, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"8.5\", \"Average atomic mass (g/mol)\": \"89.56\", \"Scarcity (wt fraction/abundance)\": \"241400.0\", \"HHI (production)\": \"2567.0\", \"HHI (reserves)\": \"1945.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1670.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00214\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.144\"}, {\"doi\": \"10.1016/j.jallcom.2006.02.075\", \"Electrical resistivity (\\u03a9cm)\": \"0.000771\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-92.0\", \"ZT\": \"0.33\", \"formula\": \"Zr0.94Y0.06Ni1Sn0.96Sb0.04\", \"comment\": \"*extrapolated from 350 K\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Katsumyama 2007\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 0.9880155642, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"8.35\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"283400.0\", \"HHI (production)\": \"2742.0\", \"HHI (reserves)\": \"1962.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1300.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0011\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8460.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.114\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00123\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-119.0\", \"ZT\": \"0.35\", \"formula\": \"Nb1Co1Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 1.0408774177, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.904\", \"Average atomic mass (g/mol)\": \"90.18\", \"Scarcity (wt fraction/abundance)\": \"221500.0\", \"HHI (production)\": \"4729.0\", \"HHI (reserves)\": \"4317.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"814.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00116\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.086\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00137\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-163.0\", \"ZT\": \"0.58\", \"formula\": \"Nb1Co1.05Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 1.7496171655, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.887\", \"Average atomic mass (g/mol)\": \"89.67\", \"Scarcity (wt fraction/abundance)\": \"219500.0\", \"HHI (production)\": \"4711.0\", \"HHI (reserves)\": \"4299.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"728.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.077\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00111\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-131.0\", \"ZT\": \"0.46\", \"formula\": \"Nb1Co1.10Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 1.3861662416, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.802\", \"Average atomic mass (g/mol)\": \"89.17\", \"Scarcity (wt fraction/abundance)\": \"217500.0\", \"HHI (production)\": \"4693.0\", \"HHI (reserves)\": \"4281.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"901.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00154\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.114\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000161\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-81.0\", \"ZT\": \"1.23\", \"formula\": \"Bi92Sb8\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"300\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 3.7022941609, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"202.0\", \"Scarcity (wt fraction/abundance)\": \"56230000.0\", \"HHI (production)\": \"5422.0\", \"HHI (reserves)\": \"5869.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"6220.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00411\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000182\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-81.0\", \"ZT\": \"1.07\", \"formula\": \"Bi90Sb10\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"300\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 3.2190394524, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"200.26\", \"Scarcity (wt fraction/abundance)\": \"55550000.0\", \"HHI (production)\": \"5455.0\", \"HHI (reserves)\": \"5836.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5490.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00358\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6520.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000172\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-85.0\", \"ZT\": \"1.27\", \"formula\": \"Bi88Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"300\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 3.804904909, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"198.51\", \"Scarcity (wt fraction/abundance)\": \"54860000.0\", \"HHI (production)\": \"5488.0\", \"HHI (reserves)\": \"5804.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5810.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00423\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7270.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000256\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-81.0\", \"ZT\": \"0.77\", \"formula\": \"Bi86Sb14\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"300\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 2.3240008227, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"196.77\", \"Scarcity (wt fraction/abundance)\": \"54160000.0\", \"HHI (production)\": \"5522.0\", \"HHI (reserves)\": \"5770.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3900.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00258\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.00026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-75.0\", \"ZT\": \"0.65\", \"formula\": \"Bi83Sb17\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"300\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 1.9621303911, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"194.15\", \"Scarcity (wt fraction/abundance)\": \"53090000.0\", \"HHI (production)\": \"5574.0\", \"HHI (reserves)\": \"5719.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3850.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00218\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5660.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.513\", \"Seebeck coefficient (\\u03bcCV/K)\": \"33.0\", \"ZT\": \"6.2e-05\", \"formula\": \"Ca1Mn6.5Cu0.5O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.05\", \"Scarcity (wt fraction/abundance)\": \"1387.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1359.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1.949\", \"Power Factor (W/(K\\u00b2m))\": \"2.07e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1060.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.248\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-13.0\", \"ZT\": \"2.09e-05\", \"formula\": \"Ca1Mn6Cu1O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.26\", \"Scarcity (wt fraction/abundance)\": \"2126.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1348.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.038\", \"Power Factor (W/(K\\u00b2m))\": \"6.97e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"173.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"1720.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-56.0\", \"ZT\": \"5.4e-08\", \"formula\": \"Li1Mn2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.000581\", \"Power Factor (W/(K\\u00b2m))\": \"1.8e-10\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.055\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-22.0\", \"ZT\": \"0.000269\", \"formula\": \"Pr0.5Ca0.5Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #85650, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.69\", \"Scarcity (wt fraction/abundance)\": \"40990.0\", \"HHI (production)\": \"4428.0\", \"HHI (reserves)\": \"1928.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"221.92\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.096\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"18.1\", \"Power Factor (W/(K\\u00b2m))\": \"8.97e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"496.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000711\", \"Seebeck coefficient (\\u03bcCV/K)\": \"4.0\", \"ZT\": \"0.000705\", \"formula\": \"Mo3Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.812\", \"Average atomic mass (g/mol)\": \"114.04\", \"Scarcity (wt fraction/abundance)\": \"639700000.0\", \"HHI (production)\": \"2718.0\", \"HHI (reserves)\": \"5052.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1410.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.35e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16.7\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.27\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000767\", \"Seebeck coefficient (\\u03bcCV/K)\": \"3.0\", \"ZT\": \"0.000439\", \"formula\": \"Mo6Te7S1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.773\", \"Average atomic mass (g/mol)\": \"107.22\", \"Scarcity (wt fraction/abundance)\": \"595400000.0\", \"HHI (production)\": \"2661.0\", \"HHI (reserves)\": \"4975.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1300.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.46e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11.2\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.344\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000857\", \"Seebeck coefficient (\\u03bcCV/K)\": \"6.0\", \"ZT\": \"0.00139\", \"formula\": \"Mo6Te6S2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.125\", \"Average atomic mass (g/mol)\": \"100.39\", \"Scarcity (wt fraction/abundance)\": \"545100000.0\", \"HHI (production)\": \"2596.0\", \"HHI (reserves)\": \"4888.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1170.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.63e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"39.7\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.402\"}, {\"doi\": \"10.1109/ICT.2006.331289\", \"Electrical resistivity (\\u03a9cm)\": \"0.00249\", \"Seebeck coefficient (\\u03bcCV/K)\": \"139.0\", \"ZT\": \"0.23\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kuriyama 2006\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.6970023365, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"402.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000774\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00476\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-54.0\", \"ZT\": \"0.02\", \"formula\": \"Sr2Ti0.8Nb0.2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.37\", \"Average atomic mass (g/mol)\": \"42.3\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3261.0\", \"HHI (reserves)\": \"2636.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"187.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.357\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"210.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.03e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2870.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.035\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00186\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-42.0\", \"ZT\": \"0.03\", \"formula\": \"Sr3Ti1.6Nb0.4O7\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.96\", \"Average atomic mass (g/mol)\": \"40.72\", \"Scarcity (wt fraction/abundance)\": \"5611.0\", \"HHI (production)\": \"3187.0\", \"HHI (reserves)\": \"2641.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"305.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.708\", \"Atoms per unit cell\": \"24.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"538.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.67e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.079\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00145\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-52.0\", \"ZT\": \"0.06\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162889, 15K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"10.42\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"240.63\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.032\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"689.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000187\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2720.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.048\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00701\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-167.0\", \"ZT\": \"0.12\", \"formula\": \"Sr0.95La0.05Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 0.3578973059, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.21\", \"Scarcity (wt fraction/abundance)\": \"2291.0\", \"HHI (production)\": \"2640.0\", \"HHI (reserves)\": \"1987.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"143.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000398\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00261\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-98.0\", \"ZT\": \"0.11\", \"formula\": \"Sr0.9La0.1Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 0.3279448636, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"5.88\", \"Average atomic mass (g/mol)\": \"37.72\", \"Scarcity (wt fraction/abundance)\": \"3205.0\", \"HHI (production)\": \"2856.0\", \"HHI (reserves)\": \"2006.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"383.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000364\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9530.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.048\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.000613\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-54.0\", \"ZT\": \"0.14\", \"formula\": \"Sr0.8La0.2Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65094, 300K\", \"marker\": \"{'radius': 0.4234006679, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.75\", \"Scarcity (wt fraction/abundance)\": \"4961.0\", \"HHI (production)\": \"3271.0\", \"HHI (reserves)\": \"2041.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.0\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1630.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00047\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2880.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.031\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-271.0\", \"ZT\": \"0.07\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.076\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"31.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000234\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"73600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00383\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00116\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-177.0\", \"ZT\": \"0.82\", \"formula\": \"Ti0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 2.4498474109, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.893\", \"Average atomic mass (g/mol)\": \"75.24\", \"Scarcity (wt fraction/abundance)\": \"236100.0\", \"HHI (production)\": \"1890.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"866.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00272\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.092\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000654\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-140.0\", \"ZT\": \"0.9\", \"formula\": \"Ti0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 2.6968857413, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.426\", \"Average atomic mass (g/mol)\": \"75.39\", \"Scarcity (wt fraction/abundance)\": \"235900.0\", \"HHI (production)\": \"1918.0\", \"HHI (reserves)\": \"1638.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1530.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.003\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.151\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000351\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-96.0\", \"ZT\": \"0.79\", \"formula\": \"Ti0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 2.3756837919, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.96\", \"Average atomic mass (g/mol)\": \"75.84\", \"Scarcity (wt fraction/abundance)\": \"235200.0\", \"HHI (production)\": \"2004.0\", \"HHI (reserves)\": \"1726.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2850.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00264\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9260.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.3\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.031\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-354.0\", \"ZT\": \"0.12\", \"formula\": \"Zr1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 0.3584016519, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"10.143\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"200100.0\", \"HHI (production)\": \"2519.0\", \"HHI (reserves)\": \"1929.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"31.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000398\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"125000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0023\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.0011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-171.0\", \"ZT\": \"0.8\", \"formula\": \"Zr0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 2.399733097, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"9.676\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200200.0\", \"HHI (production)\": \"2537.0\", \"HHI (reserves)\": \"1950.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"913.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00267\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.069\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000616\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-131.0\", \"ZT\": \"0.84\", \"formula\": \"Zr0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 2.5235935869, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"10.059\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200400.0\", \"HHI (production)\": \"2554.0\", \"HHI (reserves)\": \"1972.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1620.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0028\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.118\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000337\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-78.0\", \"ZT\": \"0.54\", \"formula\": \"Zr0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.6312776218, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"8.859\", \"Average atomic mass (g/mol)\": \"89.57\", \"Scarcity (wt fraction/abundance)\": \"200900.0\", \"HHI (production)\": \"2608.0\", \"HHI (reserves)\": \"2036.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2970.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00181\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6110.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.245\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.046\", \"Seebeck coefficient (\\u03bcCV/K)\": \"50.0\", \"ZT\": \"0.00164\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.8\", \"Power Factor (W/(K\\u00b2m))\": \"5.48e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2510.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"62.0\", \"ZT\": \"0.00284\", \"formula\": \"La0.05Ca2.85Co3.8O8.55\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.6\", \"Scarcity (wt fraction/abundance)\": \"17300.0\", \"HHI (production)\": \"2612.0\", \"HHI (reserves)\": \"1776.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.5\", \"Power Factor (W/(K\\u00b2m))\": \"9.47e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3860.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.06\", \"Seebeck coefficient (\\u03bcCV/K)\": \"60.0\", \"ZT\": \"0.00179\", \"formula\": \"La0.3Ca2.7Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"33.1\", \"Scarcity (wt fraction/abundance)\": \"18350.0\", \"HHI (production)\": \"3029.0\", \"HHI (reserves)\": \"1870.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"16.8\", \"Power Factor (W/(K\\u00b2m))\": \"5.98e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3570.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.043\", \"Seebeck coefficient (\\u03bcCV/K)\": \"65.0\", \"ZT\": \"0.00297\", \"formula\": \"La0.45Ca2.55Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"34.03\", \"Scarcity (wt fraction/abundance)\": \"18900.0\", \"HHI (production)\": \"3266.0\", \"HHI (reserves)\": \"1923.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"23.2\", \"Power Factor (W/(K\\u00b2m))\": \"9.9e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4270.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000509\", \"Seebeck coefficient (\\u03bcCV/K)\": \"22.0\", \"ZT\": \"0.03\", \"formula\": \"Cr1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #40697, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.938\", \"Average atomic mass (g/mol)\": \"58.82\", \"Scarcity (wt fraction/abundance)\": \"557400.0\", \"HHI (production)\": \"1985.0\", \"HHI (reserves)\": \"3955.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.41\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.608\", \"Atoms per unit cell\": \"15.3\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1970.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.09e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"463.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.742\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.00069\", \"Seebeck coefficient (\\u03bcCV/K)\": \"27.0\", \"ZT\": \"0.03\", \"formula\": \"Mn1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #249898, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.432\", \"Average atomic mass (g/mol)\": \"59.07\", \"Scarcity (wt fraction/abundance)\": \"554800.0\", \"HHI (production)\": \"1871.0\", \"HHI (reserves)\": \"3777.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"816.76\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.15\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1450.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000108\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"745.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.74\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.00065\", \"Seebeck coefficient (\\u03bcCV/K)\": \"23.0\", \"ZT\": \"0.02\", \"formula\": \"Fe1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #632653, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.488\", \"Average atomic mass (g/mol)\": \"59.14\", \"Scarcity (wt fraction/abundance)\": \"554000.0\", \"HHI (production)\": \"1937.0\", \"HHI (reserves)\": \"3740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"807.22\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.938\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1540.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.88e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"512.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.757\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000618\", \"Seebeck coefficient (\\u03bcCV/K)\": \"8.0\", \"ZT\": \"0.00332\", \"formula\": \"Ni2.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602930, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.714\", \"Average atomic mass (g/mol)\": \"59.35\", \"Scarcity (wt fraction/abundance)\": \"528800.0\", \"HHI (production)\": \"1782.0\", \"HHI (reserves)\": \"3642.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"801.34\", \"Average atomic volume (\\u212b\\u00b3)\": \"16.695\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1620.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.11e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"68.3\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.691\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000832\", \"Seebeck coefficient (\\u03bcCV/K)\": \"48.0\", \"ZT\": \"0.08\", \"formula\": \"Cu4.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602374, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.348\", \"Average atomic mass (g/mol)\": \"60.36\", \"Scarcity (wt fraction/abundance)\": \"465000.0\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"3380.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"853.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.807\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000275\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2280.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.653\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00371\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.06\", \"formula\": \"Ca0.9Bi0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #98592, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.591\", \"Average atomic mass (g/mol)\": \"31.98\", \"Scarcity (wt fraction/abundance)\": \"7688000.0\", \"HHI (production)\": \"2260.0\", \"HHI (reserves)\": \"1887.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.57\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.678\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"270.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000184\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6830.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.055\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00729\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-49.0\", \"ZT\": \"0.00995\", \"formula\": \"Ca0.9Ce0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.6\", \"Scarcity (wt fraction/abundance)\": \"1819.0\", \"HHI (production)\": \"2506.0\", \"HHI (reserves)\": \"1440.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"137.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.32e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2420.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-87.0\", \"ZT\": \"0.01\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"56.3\", \"Power Factor (W/(K\\u00b2m))\": \"4.23e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7510.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00863\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-102.0\", \"ZT\": \"0.04\", \"formula\": \"Ca0.9Sm0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.81\", \"Scarcity (wt fraction/abundance)\": \"15330.0\", \"HHI (production)\": \"2553.0\", \"HHI (reserves)\": \"1451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"116.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000121\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.462\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-70.0\", \"ZT\": \"0.000317\", \"formula\": \"Ca0.9Sb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.24\", \"Scarcity (wt fraction/abundance)\": \"403100.0\", \"HHI (production)\": \"2295.0\", \"HHI (reserves)\": \"1442.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.164\", \"Power Factor (W/(K\\u00b2m))\": \"1.06e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4890.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00796\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-93.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9La0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.58\", \"Scarcity (wt fraction/abundance)\": \"2861.0\", \"HHI (production)\": \"2501.0\", \"HHI (reserves)\": \"1438.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"126.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000109\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8650.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.045\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-274.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.9Pb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.95\", \"Scarcity (wt fraction/abundance)\": \"11170.0\", \"HHI (production)\": \"1922.0\", \"HHI (reserves)\": \"1336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"22.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000169\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"75200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.215\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-348.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.9In0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.1\", \"Scarcity (wt fraction/abundance)\": \"372600.0\", \"HHI (production)\": \"1921.0\", \"HHI (reserves)\": \"1325.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.651\", \"Power Factor (W/(K\\u00b2m))\": \"5.65e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"121000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"2.198\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-284.0\", \"ZT\": \"0.0011\", \"formula\": \"Ca0.9Sn0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"35350.0\", \"HHI (production)\": \"1866.0\", \"HHI (reserves)\": \"1298.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.455\", \"Power Factor (W/(K\\u00b2m))\": \"3.67e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"80600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"6.975\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-477.0\", \"ZT\": \"0.000977\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.99\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.143\", \"Power Factor (W/(K\\u00b2m))\": \"3.26e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"227000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"3.51e-05\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"18.4\", \"Seebeck coefficient (\\u03bcCV/K)\": \"1235.0\", \"ZT\": \"0.00249\", \"formula\": \"Cu1Cr1O2\", \"comment\": \"*res data at 300K/400K extrapolated from 600K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157800, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.586\", \"Average atomic mass (g/mol)\": \"36.88\", \"Scarcity (wt fraction/abundance)\": \"8516.0\", \"HHI (production)\": \"1881.0\", \"HHI (reserves)\": \"2193.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.054\", \"Power Factor (W/(K\\u00b2m))\": \"8.31e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1530000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"6.05e-06\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"6.112\", \"Seebeck coefficient (\\u03bcCV/K)\": \"525.0\", \"ZT\": \"0.00135\", \"formula\": \"Cu1Cr0.99Mg0.01O2\", \"comment\": \"*res data at 300K/400K extrapolated from 600K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157801, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.966\", \"Average atomic mass (g/mol)\": \"36.82\", \"Scarcity (wt fraction/abundance)\": \"8514.0\", \"HHI (production)\": \"1882.0\", \"HHI (reserves)\": \"2184.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.164\", \"Power Factor (W/(K\\u00b2m))\": \"4.51e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"276000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.72e-05\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"1.045\", \"Seebeck coefficient (\\u03bcCV/K)\": \"312.0\", \"ZT\": \"0.00279\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"7.558\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.957\", \"Power Factor (W/(K\\u00b2m))\": \"9.29e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"97100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"9.27e-05\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.102\", \"Seebeck coefficient (\\u03bcCV/K)\": \"199.0\", \"ZT\": \"0.01\", \"formula\": \"Cu1Cr0.97Mg0.03O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157803, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"7.14\", \"Average atomic mass (g/mol)\": \"36.68\", \"Scarcity (wt fraction/abundance)\": \"8511.0\", \"HHI (production)\": \"1885.0\", \"HHI (reserves)\": \"2165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.928\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.829\", \"Power Factor (W/(K\\u00b2m))\": \"3.89e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"39600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00101\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.107\", \"Seebeck coefficient (\\u03bcCV/K)\": \"197.0\", \"ZT\": \"0.01\", \"formula\": \"Cu1Cr0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157804, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"9.293\", \"Average atomic mass (g/mol)\": \"36.61\", \"Scarcity (wt fraction/abundance)\": \"8509.0\", \"HHI (production)\": \"1886.0\", \"HHI (reserves)\": \"2156.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.933\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.374\", \"Power Factor (W/(K\\u00b2m))\": \"3.63e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000738\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.075\", \"Seebeck coefficient (\\u03bcCV/K)\": \"208.0\", \"ZT\": \"0.02\", \"formula\": \"Cu1Cr0.95Mg0.05O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157805, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"9.522\", \"Average atomic mass (g/mol)\": \"36.54\", \"Scarcity (wt fraction/abundance)\": \"8507.0\", \"HHI (production)\": \"1887.0\", \"HHI (reserves)\": \"2146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.16\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.93\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"13.3\", \"Power Factor (W/(K\\u00b2m))\": \"5.74e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"43300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00102\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.000295\", \"Seebeck coefficient (\\u03bcCV/K)\": \"82.0\", \"ZT\": \"0.68\", \"formula\": \"Na1Co2O4\", \"comment\": \"\", \"synthesis\": \"flux (NaCl), air\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 2.0477778155, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"19.08\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3390.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00228\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6710.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.13\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.00211\", \"Seebeck coefficient (\\u03bcCV/K)\": \"104.0\", \"ZT\": \"0.15\", \"formula\": \"Na1Co2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 0.4622222222, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.904\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"475.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000514\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.183\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00975\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-179.0\", \"ZT\": \"0.1\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"4.087\", \"Average atomic mass (g/mol)\": \"104.09\", \"Scarcity (wt fraction/abundance)\": \"262000.0\", \"HHI (production)\": \"2643.0\", \"HHI (reserves)\": \"2022.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"103.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000328\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"32000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.018\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00904\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-189.0\", \"ZT\": \"0.12\", \"formula\": \"Zr0.4Hf0.4Ti0.2Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 0.3542234844, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.814\", \"Average atomic mass (g/mol)\": \"98.29\", \"Scarcity (wt fraction/abundance)\": \"258100.0\", \"HHI (production)\": \"2524.0\", \"HHI (reserves)\": \"1954.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"111.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000394\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.021\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00861\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-370.0\", \"ZT\": \"0.48\", \"formula\": \"Zr0.35Hf0.35Ti0.3Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.4311492988, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.17\", \"Average atomic mass (g/mol)\": \"95.39\", \"Scarcity (wt fraction/abundance)\": \"256000.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"116.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00159\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"137000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.027\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00476\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-312.0\", \"ZT\": \"0.61\", \"formula\": \"Zr0.25Hf0.25Ti0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.8365463631, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.063\", \"Average atomic mass (g/mol)\": \"89.59\", \"Scarcity (wt fraction/abundance)\": \"251300.0\", \"HHI (production)\": \"2315.0\", \"HHI (reserves)\": \"1836.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"210.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00204\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"97100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.05\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00481\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-252.0\", \"ZT\": \"0.4\", \"formula\": \"Zr0.15Hf0.15Ti0.7Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.1890120021, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.394\", \"Average atomic mass (g/mol)\": \"83.79\", \"Scarcity (wt fraction/abundance)\": \"246000.0\", \"HHI (production)\": \"2152.0\", \"HHI (reserves)\": \"1744.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"208.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00132\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"63600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.045\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.000993\", \"Seebeck coefficient (\\u03bcCV/K)\": \"68.0\", \"ZT\": \"0.14\", \"formula\": \"Ce1Fe4Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #621065, 300K\", \"marker\": \"{'radius': 0.4222149768, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.33\", \"Scarcity (wt fraction/abundance)\": \"4005000.0\", \"HHI (production)\": \"7355.0\", \"HHI (reserves)\": \"3146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"762.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.421\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1010.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000469\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4660.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00147\", \"Seebeck coefficient (\\u03bcCV/K)\": \"87.0\", \"ZT\": \"0.15\", \"formula\": \"Ce1Fe3Co1Sb12\", \"comment\": \"Unit Cell =Ce0.78 (Fe3.07 Co0.93) Sb11.69\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.4578165977, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.37\", \"Average atomic mass (g/mol)\": \"107.51\", \"Scarcity (wt fraction/abundance)\": \"4000000.0\", \"HHI (production)\": \"7367.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"679.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000509\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7490.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.363\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00274\", \"Seebeck coefficient (\\u03bcCV/K)\": \"104.0\", \"ZT\": \"0.12\", \"formula\": \"Ce1Fe2.5Co1.5Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.3572873484, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.6\", \"Scarcity (wt fraction/abundance)\": \"3997000.0\", \"HHI (production)\": \"7373.0\", \"HHI (reserves)\": \"3204.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"365.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000397\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00473\", \"Seebeck coefficient (\\u03bcCV/K)\": \"108.0\", \"ZT\": \"0.07\", \"formula\": \"Ce1Fe2Co2Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.69\", \"Scarcity (wt fraction/abundance)\": \"3994000.0\", \"HHI (production)\": \"7379.0\", \"HHI (reserves)\": \"3223.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"211.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000245\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-87.0\", \"ZT\": \"0.02\", \"formula\": \"Ce1Fe1Co3Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.88\", \"Scarcity (wt fraction/abundance)\": \"3988000.0\", \"HHI (production)\": \"7391.0\", \"HHI (reserves)\": \"3261.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"95.7\", \"Power Factor (W/(K\\u00b2m))\": \"7.24e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7570.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.061\", \"Seebeck coefficient (\\u03bcCV/K)\": \"16.0\", \"ZT\": \"0.000131\", \"formula\": \"Ce1Fe1.5Co2.5Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.78\", \"Scarcity (wt fraction/abundance)\": \"3991000.0\", \"HHI (production)\": \"7385.0\", \"HHI (reserves)\": \"3242.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"16.4\", \"Power Factor (W/(K\\u00b2m))\": \"4.38e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"267.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00164\", \"Seebeck coefficient (\\u03bcCV/K)\": \"108.0\", \"ZT\": \"0.21\", \"formula\": \"La1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #280118, 295K\", \"marker\": \"{'radius': 0.6435399798, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.6\", \"Average atomic mass (g/mol)\": \"107.44\", \"Scarcity (wt fraction/abundance)\": \"4003000.0\", \"HHI (production)\": \"7366.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"752.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.143\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"609.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000715\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.278\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00932\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-177.0\", \"ZT\": \"0.1\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 0.303279806, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.949\", \"Average atomic mass (g/mol)\": \"104.09\", \"Scarcity (wt fraction/abundance)\": \"262000.0\", \"HHI (production)\": \"2643.0\", \"HHI (reserves)\": \"2022.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"107.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000337\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.02\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00241\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-250.0\", \"ZT\": \"0.78\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1.998Sb0.002\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 2.3359634551, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.887\", \"Average atomic mass (g/mol)\": \"107.74\", \"Scarcity (wt fraction/abundance)\": \"314900.0\", \"HHI (production)\": \"2632.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"415.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0026\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"62500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.105\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00117\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-211.0\", \"ZT\": \"1.15\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1.994Sb0.006\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 3.4364408233, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.767\", \"Average atomic mass (g/mol)\": \"107.75\", \"Scarcity (wt fraction/abundance)\": \"320000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"1919.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"858.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00382\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.227\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00877\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-182.0\", \"ZT\": \"0.11\", \"formula\": \"Zr0.4Hf0.4Ti0.2Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 0.3389485471, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"98.29\", \"Scarcity (wt fraction/abundance)\": \"258100.0\", \"HHI (production)\": \"2524.0\", \"HHI (reserves)\": \"1954.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"114.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000377\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"33000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00841\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-330.0\", \"ZT\": \"0.39\", \"formula\": \"Zr0.35Hf0.35Ti0.3Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.1633861235, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"95.39\", \"Scarcity (wt fraction/abundance)\": \"256000.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"119.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00129\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"109000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00846\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-316.0\", \"ZT\": \"0.35\", \"formula\": \"Zr0.3Hf0.3Ti0.4Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.0637609836, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"92.49\", \"Scarcity (wt fraction/abundance)\": \"253700.0\", \"HHI (production)\": \"2389.0\", \"HHI (reserves)\": \"1878.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"118.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00118\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"100000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00495\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-304.0\", \"ZT\": \"0.56\", \"formula\": \"Zr0.25Hf0.25Ti0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.6757988487, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"89.59\", \"Scarcity (wt fraction/abundance)\": \"251300.0\", \"HHI (production)\": \"2315.0\", \"HHI (reserves)\": \"1836.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"202.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00186\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"92200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00467\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-251.0\", \"ZT\": \"0.4\", \"formula\": \"Zr0.15Hf0.15Ti0.7Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.2105126821, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"83.79\", \"Scarcity (wt fraction/abundance)\": \"246000.0\", \"HHI (production)\": \"2152.0\", \"HHI (reserves)\": \"1744.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"214.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00135\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"62900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://orbit.dtu.dk/en/publications/improvement-of-niobium-doped-srtio3-by-nanostructuring(2b6f4b33-1a6f-4472-ac18-6996f91cd743).html\", \"Electrical resistivity (\\u03a9cm)\": \"0.00462\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-64.0\", \"ZT\": \"0.03\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"Unit cell=Sr0.8 Ti0.6 Nb0.4 O3\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sonne 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"7.96\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"217.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.74e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4040.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.02\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00962\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-50.0\", \"ZT\": \"0.00771\", \"formula\": \"Sr1Dy0.08Ti0.92O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.195\", \"Average atomic mass (g/mol)\": \"38.53\", \"Scarcity (wt fraction/abundance)\": \"13120.0\", \"HHI (production)\": \"2920.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"104.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.57e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2470.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.018\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.0026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-32.0\", \"ZT\": \"0.01\", \"formula\": \"Sr1Nd0.17Ti0.83O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.19\", \"Average atomic mass (g/mol)\": \"39.97\", \"Scarcity (wt fraction/abundance)\": \"4528.0\", \"HHI (production)\": \"3337.0\", \"HHI (reserves)\": \"2128.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"385.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.07e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1060.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.046\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00184\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-34.0\", \"ZT\": \"0.02\", \"formula\": \"Sr1Nd0.2Ti0.8O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.53\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3484.0\", \"HHI (reserves)\": \"2153.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"544.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.44e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1180.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.072\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00225\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-23.0\", \"ZT\": \"0.00682\", \"formula\": \"Sr1Nd0.24Ti0.76O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.98\", \"Average atomic mass (g/mol)\": \"41.32\", \"Scarcity (wt fraction/abundance)\": \"5689.0\", \"HHI (production)\": \"3673.0\", \"HHI (reserves)\": \"2186.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"445.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.27e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"511.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.054\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00231\", \"Seebeck coefficient (\\u03bcCV/K)\": \"122.0\", \"ZT\": \"0.19\", \"formula\": \"Zn4Sb3\", \"comment\": \"Unit Cell = (Zn4 Sb3)1.04\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 0.5814355137, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.77\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"433.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000646\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.412\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00213\", \"Seebeck coefficient (\\u03bcCV/K)\": \"127.0\", \"ZT\": \"0.23\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 0.6815940098, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.76\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"470.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000757\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.453\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"136.0\", \"ZT\": \"0.25\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 0.7647174546, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.783\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"460.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00085\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.43\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.26\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-301.0\", \"ZT\": \"0.01\", \"formula\": \"Zn1O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"48.7\", \"Average atomic mass (g/mol)\": \"40.69\", \"Scarcity (wt fraction/abundance)\": \"10780.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1621.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.059\", \"Power Factor (W/(K\\u00b2m))\": \"3.49e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"90600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"8.89e-07\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00562\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-154.0\", \"ZT\": \"0.13\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.3796715247, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"44.495\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"155.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000422\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00254\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00275\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-179.0\", \"ZT\": \"0.35\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.0453557345, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"44.495\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"312.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00116\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"32000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00513\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.0012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-138.0\", \"ZT\": \"0.47\", \"formula\": \"Zn0.98Al0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.4238335397, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"40.29\", \"Average atomic mass (g/mol)\": \"40.31\", \"Scarcity (wt fraction/abundance)\": \"10670.0\", \"HHI (production)\": \"1361.0\", \"HHI (reserves)\": \"1612.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"779.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00158\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.014\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00132\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-175.0\", \"ZT\": \"0.7\", \"formula\": \"Zn0.95Al0.05O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 2.086697616, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"34.5\", \"Average atomic mass (g/mol)\": \"39.73\", \"Scarcity (wt fraction/abundance)\": \"10490.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1599.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"690.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00232\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.015\"}, {\"doi\": \"10.1016/j.jallcom.2010.06.195\", \"Electrical resistivity (\\u03a9cm)\": \"5.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-40.0\", \"ZT\": \"9.35e-06\", \"formula\": \"Sr1Nb0.15Ti0.85O3\", \"comment\": \"Unit cell=Sr0.8 Ti0.6 Nb0.4 O3\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wang 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"5.88\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"5257.0\", \"HHI (production)\": \"2915.0\", \"HHI (reserves)\": \"2484.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.199\", \"Power Factor (W/(K\\u00b2m))\": \"3.12e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1560.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"2.48e-05\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.00066\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-43.0\", \"ZT\": \"0.08\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"*Seebeck extrapolated from 350K\", \"synthesis\": \"Czochralski method, He\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.7\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1520.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000277\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1830.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.652\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.000782\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-50.0\", \"ZT\": \"0.09\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.52\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1280.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000315\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2470.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.616\"}, {\"doi\": \"10.1126/science.287.5455.1024\", \"Electrical resistivity (\\u03a9cm)\": \"0.000774\", \"Seebeck coefficient (\\u03bcCV/K)\": \"105.0\", \"ZT\": \"0.43\", \"formula\": \"Cs1Bi4Te6\", \"comment\": \"\", \"synthesis\": \"melted, air\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Chung 2000\", \"Structure\": \"ICSD #170576, 300K\", \"marker\": \"{'radius': 1.2893127907, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"157.68\", \"Scarcity (wt fraction/abundance)\": \"469800000.0\", \"HHI (production)\": \"4289.0\", \"HHI (reserves)\": \"5526.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"3250.47\", \"Average atomic volume (\\u212b\\u00b3)\": \"36.937\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1290.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00143\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1126/science.287.5455.1024\", \"Electrical resistivity (\\u03a9cm)\": \"0.00085\", \"Seebeck coefficient (\\u03bcCV/K)\": \"154.0\", \"ZT\": \"0.84\", \"formula\": \"Sb0.005I0.015Cs0.995Bi3.98Te5.97\", \"comment\": \"\", \"synthesis\": \"melted, air\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Chung 2000\", \"Structure\": \"ICSD #170576, 300K\", \"marker\": \"{'radius': 2.5176324706, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.5\", \"Average atomic mass (g/mol)\": \"157.62\", \"Scarcity (wt fraction/abundance)\": \"469100000.0\", \"HHI (production)\": \"4291.0\", \"HHI (reserves)\": \"5525.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"3250.47\", \"Average atomic volume (\\u212b\\u00b3)\": \"36.937\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1180.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0028\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.574\"}, {\"doi\": \"10.1063/1.2163979\", \"Electrical resistivity (\\u03a9cm)\": \"0.000662\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-50.0\", \"ZT\": \"0.11\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"Czochralski method, argon\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Saramat 2006\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.3398791541, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.94\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1510.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000378\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.57\"}, {\"doi\": \"10.1103/PhysRevLett.86.4350\", \"Electrical resistivity (\\u03a9cm)\": \"0.00642\", \"Seebeck coefficient (\\u03bcCV/K)\": \"256.0\", \"ZT\": \"0.31\", \"formula\": \"Tl9Bi1Te6\", \"comment\": \"\", \"synthesis\": \"melted, zone refined\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wolfing 2001\", \"Structure\": \"ICSD #400246, 300K\", \"marker\": \"{'radius': 0.918728972, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.481\", \"Average atomic mass (g/mol)\": \"175.88\", \"Scarcity (wt fraction/abundance)\": \"277400000.0\", \"HHI (production)\": \"5429.0\", \"HHI (reserves)\": \"6036.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1025.05\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.033\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"156.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00102\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"65500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.237\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.000324\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-41.0\", \"ZT\": \"0.16\", \"formula\": \"Bi1.2S1.2Ti2S4\", \"comment\": \"*extrapolated from 322 K\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 0.4738027778, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.94\", \"Average atomic mass (g/mol)\": \"61.1\", \"Scarcity (wt fraction/abundance)\": \"28740000.0\", \"HHI (production)\": \"3036.0\", \"HHI (reserves)\": \"3543.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3090.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000526\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1710.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.768\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.00046\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-51.0\", \"ZT\": \"0.17\", \"formula\": \"Pb1.8S1.8Ti2S4\", \"comment\": \"*extrapolated from 322 K\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 0.5049078261, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.9\", \"Average atomic mass (g/mol)\": \"68.19\", \"Scarcity (wt fraction/abundance)\": \"48160.0\", \"HHI (production)\": \"1920.0\", \"HHI (reserves)\": \"1526.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2170.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000561\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2580.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.549\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.000478\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-65.0\", \"ZT\": \"0.26\", \"formula\": \"Sn1.2S1.2Ti2S4\", \"comment\": \"*extrapolated from 322 K\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 0.7906142259, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.66\", \"Average atomic mass (g/mol)\": \"48.21\", \"Scarcity (wt fraction/abundance)\": \"157400.0\", \"HHI (production)\": \"1480.0\", \"HHI (reserves)\": \"1355.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2090.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000878\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.576\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.0033\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-102.0\", \"ZT\": \"0.09\", \"formula\": \"Ba8Au5.14Si39.51\", \"comment\": \"*extrapolated from 312 K\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"300\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.86\", \"Average atomic mass (g/mol)\": \"61.17\", \"Scarcity (wt fraction/abundance)\": \"78590000.0\", \"HHI (production)\": \"2988.0\", \"HHI (reserves)\": \"1472.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"303.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000315\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.119\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.00234\", \"Seebeck coefficient (\\u03bcCV/K)\": \"106.0\", \"ZT\": \"0.14\", \"formula\": \"Ba8Au5.59Si39.01\", \"comment\": \"*extrapolated from 312 K\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"300\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 0.4337861538, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.77\", \"Average atomic mass (g/mol)\": \"62.65\", \"Scarcity (wt fraction/abundance)\": \"83530000.0\", \"HHI (production)\": \"2930.0\", \"HHI (reserves)\": \"1462.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"427.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000482\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.177\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.000617\", \"Seebeck coefficient (\\u03bcCV/K)\": \"46.0\", \"ZT\": \"0.1\", \"formula\": \"Ba8Au6.10Si38.97\", \"comment\": \"*extrapolated from 312 K\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"300\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 0.3118839287, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.18\", \"Average atomic mass (g/mol)\": \"63.97\", \"Scarcity (wt fraction/abundance)\": \"88490000.0\", \"HHI (production)\": \"2876.0\", \"HHI (reserves)\": \"1450.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1620.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000347\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2140.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.544\"}, {\"doi\": \"10.1002/chin.199644003\", \"Electrical resistivity (\\u03a9cm)\": \"0.165\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-25.0\", \"ZT\": \"0.000114\", \"formula\": \"K1Bi6.33S10\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kanatizidis 1996\", \"Structure\": \"ICSD #79200, 296K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.3\", \"Average atomic mass (g/mol)\": \"97.09\", \"Scarcity (wt fraction/abundance)\": \"46250000.0\", \"HHI (production)\": \"4345.0\", \"HHI (reserves)\": \"5070.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1204.18\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.449\", \"Atoms per unit cell\": \"36.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"6.061\", \"Power Factor (W/(K\\u00b2m))\": \"3.79e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"625.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00341\"}, {\"doi\": \"10.1021/cm050412c\", \"Electrical resistivity (\\u03a9cm)\": \"0.21\", \"Seebeck coefficient (\\u03bcCV/K)\": \"220.0\", \"ZT\": \"0.00691\", \"formula\": \"Tl11.5Sb11.5Cu8Se27\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"McGuire 2005\", \"Structure\": \"ICSD #171227, 175K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"110.19\", \"Scarcity (wt fraction/abundance)\": \"8301000.0\", \"HHI (production)\": \"4990.0\", \"HHI (reserves)\": \"3898.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1468.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.31\", \"Atoms per unit cell\": \"58.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.762\", \"Power Factor (W/(K\\u00b2m))\": \"2.3e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1021/cm050412c\", \"Electrical resistivity (\\u03a9cm)\": \"14500.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-160.0\", \"ZT\": \"5.3e-08\", \"formula\": \"Tl1Ti1P1S5\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"McGuire 2005\", \"Structure\": \"ICSD #171214, 175K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.783\", \"Average atomic mass (g/mol)\": \"55.44\", \"Scarcity (wt fraction/abundance)\": \"668700.0\", \"HHI (production)\": \"3519.0\", \"HHI (reserves)\": \"3878.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"374.96\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.435\", \"Atoms per unit cell\": \"16.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"6.9e-05\", \"Power Factor (W/(K\\u00b2m))\": \"1.77e-10\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"6.45e-08\"}, {\"doi\": \"10.1021/cm050412c\", \"Electrical resistivity (\\u03a9cm)\": \"130.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"345.0\", \"ZT\": \"2.75e-05\", \"formula\": \"Tl2Cu2Sn1Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"McGuire 2005\", \"Structure\": \"ICSD #171222, 175K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.377\", \"Average atomic mass (g/mol)\": \"129.44\", \"Scarcity (wt fraction/abundance)\": \"438700000.0\", \"HHI (production)\": \"3984.0\", \"HHI (reserves)\": \"4776.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"500.1\", \"Average atomic volume (\\u212b\\u00b3)\": \"27.783\", \"Atoms per unit cell\": \"18.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00769\", \"Power Factor (W/(K\\u00b2m))\": \"9.16e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"119000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.49e-05\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.00145\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-151.0\", \"ZT\": \"0.47\", \"formula\": \"Mg2Si0.999Bi0.001\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.4191493776, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"8.52\", \"Average atomic mass (g/mol)\": \"25.63\", \"Scarcity (wt fraction/abundance)\": \"159900.0\", \"HHI (production)\": \"5058.0\", \"HHI (reserves)\": \"697.4\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"692.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00158\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.059\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.00082\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-107.0\", \"ZT\": \"0.42\", \"formula\": \"Mg2Si0.9985Bi0.0015\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.256597561, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"7.08\", \"Average atomic mass (g/mol)\": \"25.66\", \"Scarcity (wt fraction/abundance)\": \"239600.0\", \"HHI (production)\": \"5058.0\", \"HHI (reserves)\": \"704.6\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1220.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0014\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.126\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000488\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-77.0\", \"ZT\": \"0.36\", \"formula\": \"Mg2Si0.997Bi0.003\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.0821319672, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"6.16\", \"Average atomic mass (g/mol)\": \"25.75\", \"Scarcity (wt fraction/abundance)\": \"477500.0\", \"HHI (production)\": \"5060.0\", \"HHI (reserves)\": \"725.9\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2050.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0012\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5870.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.244\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000369\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-68.0\", \"ZT\": \"0.37\", \"formula\": \"Mg2Si0.995Bi0.005\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.1178756098, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"6.55\", \"Average atomic mass (g/mol)\": \"25.87\", \"Scarcity (wt fraction/abundance)\": \"792100.0\", \"HHI (production)\": \"5061.0\", \"HHI (reserves)\": \"754.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2710.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00124\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4580.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.303\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.00033\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-61.0\", \"ZT\": \"0.34\", \"formula\": \"Mg2Si0.994Bi0.006\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.0148181818, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"6.55\", \"Average atomic mass (g/mol)\": \"25.93\", \"Scarcity (wt fraction/abundance)\": \"948300.0\", \"HHI (production)\": \"5062.0\", \"HHI (reserves)\": \"768.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3030.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00113\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3720.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.339\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.00152\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.14\", \"formula\": \"Mg2Si0.98Bi0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.4069190132, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"7.13\", \"Average atomic mass (g/mol)\": \"26.77\", \"Scarcity (wt fraction/abundance)\": \"3061000.0\", \"HHI (production)\": \"5072.0\", \"HHI (reserves)\": \"957.2\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"658.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000452\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6870.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.068\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.0015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.14\", \"formula\": \"Mg2Si0.6Ge0.4Bi0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 0.41334, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.98\", \"Average atomic mass (g/mol)\": \"32.68\", \"Scarcity (wt fraction/abundance)\": \"2694000.0\", \"HHI (production)\": \"5169.0\", \"HHI (reserves)\": \"1229.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"667.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000459\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6890.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.164\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"1.24\", \"Seebeck coefficient (\\u03bcCV/K)\": \"26.0\", \"ZT\": \"1.64e-05\", \"formula\": \"Mg2Si0.98Ag0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"7.83\", \"Average atomic mass (g/mol)\": \"26.1\", \"Scarcity (wt fraction/abundance)\": \"353300.0\", \"HHI (production)\": \"4954.0\", \"HHI (reserves)\": \"699.7\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.806\", \"Power Factor (W/(K\\u00b2m))\": \"5.45e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"676.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"7.54e-05\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.051\", \"Seebeck coefficient (\\u03bcCV/K)\": \"30.0\", \"ZT\": \"0.000541\", \"formula\": \"Mg2Si0.6Ge0.4Ag0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.11\", \"Average atomic mass (g/mol)\": \"32.01\", \"Scarcity (wt fraction/abundance)\": \"493400.0\", \"HHI (production)\": \"5075.0\", \"HHI (reserves)\": \"1026.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"19.5\", \"Power Factor (W/(K\\u00b2m))\": \"1.8e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"925.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00347\"}, {\"doi\": \"10.1063/1.2009828\", \"Electrical resistivity (\\u03a9cm)\": \"0.254\", \"Seebeck coefficient (\\u03bcCV/K)\": \"388.0\", \"ZT\": \"0.02\", \"formula\": \"Ag9Tl1Te5\", \"comment\": \"*extrapolated from 342 K\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kurosaki 2005\", \"Structure\": \"ICSD #71689, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.2\", \"Average atomic mass (g/mol)\": \"120.88\", \"Scarcity (wt fraction/abundance)\": \"358900000.0\", \"HHI (production)\": \"2408.0\", \"HHI (reserves)\": \"3201.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"4758.66\", \"Average atomic volume (\\u212b\\u00b3)\": \"27.349\", \"Atoms per unit cell\": \"174.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.931\", \"Power Factor (W/(K\\u00b2m))\": \"5.92e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"151000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.014\"}, {\"doi\": \"10.1063/1.124182\", \"Electrical resistivity (\\u03a9cm)\": \"0.0042\", \"Seebeck coefficient (\\u03bcCV/K)\": \"219.0\", \"ZT\": \"0.34\", \"formula\": \"Tl2Sn1Te5\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sharp 1999\", \"Structure\": \"ICSD #73666, 294K\", \"marker\": \"{'radius': 1.0277357143, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"5.09\", \"Average atomic mass (g/mol)\": \"145.68\", \"Scarcity (wt fraction/abundance)\": \"548000000.0\", \"HHI (production)\": \"4127.0\", \"HHI (reserves)\": \"5148.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1045.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.686\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"238.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00114\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.034\"}, {\"doi\": \"10.1063/1.124182\", \"Electrical resistivity (\\u03a9cm)\": \"0.023\", \"Seebeck coefficient (\\u03bcCV/K)\": \"285.0\", \"ZT\": \"0.11\", \"formula\": \"Tl2Ge1Te5\", \"comment\": \"*kappa extrapolated from 250 K\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sharp 1999\", \"Structure\": \"ICSD #68855, 300K\", \"marker\": \"{'radius': 0.3159140017, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"9.07\", \"Average atomic mass (g/mol)\": \"139.93\", \"Scarcity (wt fraction/abundance)\": \"570500000.0\", \"HHI (production)\": \"4364.0\", \"HHI (reserves)\": \"5309.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"2027.01\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.672\", \"Atoms per unit cell\": \"64.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"43.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000351\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"81200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00349\"}, {\"doi\": \"10.1063/1.124182\", \"Electrical resistivity (\\u03a9cm)\": \"0.00433\", \"Seebeck coefficient (\\u03bcCV/K)\": \"163.0\", \"ZT\": \"0.18\", \"formula\": \"Tl2Sn1Te5\", \"comment\": \"\", \"synthesis\": \"melted, hotpressed\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Sharp 1999\", \"Structure\": \"ICSD #73666, 294K\", \"marker\": \"{'radius': 0.5522424942, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"6.75\", \"Average atomic mass (g/mol)\": \"145.68\", \"Scarcity (wt fraction/abundance)\": \"548000000.0\", \"HHI (production)\": \"4127.0\", \"HHI (reserves)\": \"5148.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1045.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.686\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"231.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000614\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.025\"}, {\"doi\": \"10.1063/1.124182\", \"Electrical resistivity (\\u03a9cm)\": \"0.00321\", \"Seebeck coefficient (\\u03bcCV/K)\": \"145.0\", \"ZT\": \"0.2\", \"formula\": \"Tl2Sn1Te5\", \"comment\": \"\", \"synthesis\": \"flux (TlTe2)\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Sharp 1999\", \"Structure\": \"ICSD #73666, 294K\", \"marker\": \"{'radius': 0.5894859813, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"145.68\", \"Scarcity (wt fraction/abundance)\": \"548000000.0\", \"HHI (production)\": \"4127.0\", \"HHI (reserves)\": \"5148.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1045.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.686\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"312.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000655\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.121747\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-320.0\", \"ZT\": \"0.24\", \"formula\": \"Sr0.145Ga0.302Ge0.553\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nolas 1998\", \"Structure\": \"ICSD #90177, 295K\", \"marker\": \"{'radius': 0.7144186047, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.81\", \"Average atomic mass (g/mol)\": \"73.93\", \"Scarcity (wt fraction/abundance)\": \"390200.0\", \"HHI (production)\": \"5146.0\", \"HHI (reserves)\": \"2085.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1233.18\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.691\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"77.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000794\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"102000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.07\"}, {\"doi\": \"10.1063/1.121747\", \"Electrical resistivity (\\u03a9cm)\": \"0.00262\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-154.0\", \"ZT\": \"0.27\", \"formula\": \"Sr0.147Ga0.298Ge0.555\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nolas 1998\", \"Structure\": \"ICSD #90177, 295K\", \"marker\": \"{'radius': 0.8146717557, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.216\", \"Average atomic mass (g/mol)\": \"73.97\", \"Scarcity (wt fraction/abundance)\": \"391100.0\", \"HHI (production)\": \"5143.0\", \"HHI (reserves)\": \"2087.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1233.18\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.691\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"382.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000905\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.23\"}, {\"doi\": \"10.1063/1.121747\", \"Electrical resistivity (\\u03a9cm)\": \"0.00194\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-128.0\", \"ZT\": \"0.25\", \"formula\": \"Sr0.146Ga0.285Ge0.569\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Nolas 1998\", \"Structure\": \"ICSD #90177, 295K\", \"marker\": \"{'radius': 0.7600824742, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.06\", \"Average atomic mass (g/mol)\": \"74.0\", \"Scarcity (wt fraction/abundance)\": \"399800.0\", \"HHI (production)\": \"5141.0\", \"HHI (reserves)\": \"2086.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1233.18\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.691\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"515.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000845\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.356\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00282\", \"Seebeck coefficient (\\u03bcCV/K)\": \"149.0\", \"ZT\": \"0.24\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"*kappa extrapolated\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.7092971246, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"355.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000788\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.13\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00776\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-79.0\", \"ZT\": \"0.02\", \"formula\": \"Ba8Ga18Ge28\", \"comment\": \"\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.5\", \"Average atomic mass (g/mol)\": \"81.25\", \"Scarcity (wt fraction/abundance)\": \"335300.0\", \"HHI (production)\": \"4759.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"129.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.02e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6230.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.063\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-189.0\", \"ZT\": \"0.1\", \"formula\": \"Ba8Ga16Sn30\", \"comment\": \"*value at 920 K\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #161949, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"106.95\", \"Scarcity (wt fraction/abundance)\": \"284700.0\", \"HHI (production)\": \"3226.0\", \"HHI (reserves)\": \"1823.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1595.46\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.546\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"90.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.00032\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.000786\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-72.0\", \"ZT\": \"0.2\", \"formula\": \"Sr8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #90177, 295K\", \"marker\": \"{'radius': 0.5919400763, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"73.99\", \"Scarcity (wt fraction/abundance)\": \"391300.0\", \"HHI (production)\": \"5141.0\", \"HHI (reserves)\": \"2089.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1233.18\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.837\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1270.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000658\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5170.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.000669\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-62.0\", \"ZT\": \"0.17\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.5171300448, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1490.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000575\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3840.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.00122\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-49.0\", \"ZT\": \"0.06\", \"formula\": \"Ba8Ga16Si30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.61\", \"Scarcity (wt fraction/abundance)\": \"20060.0\", \"HHI (production)\": \"4373.0\", \"HHI (reserves)\": \"1811.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"820.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000199\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2430.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00162\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.15\", \"formula\": \"Mg2Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.4392421442, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.5\", \"Average atomic mass (g/mol)\": \"25.57\", \"Scarcity (wt fraction/abundance)\": \"27.34\", \"HHI (production)\": \"5057.0\", \"HHI (reserves)\": \"683.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"616.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000488\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7920.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.1\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00104\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-75.0\", \"ZT\": \"0.16\", \"formula\": \"Mg1.95Ca0.05Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.4855868852, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.6\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"27.02\", \"HHI (production)\": \"5023.0\", \"HHI (reserves)\": \"707.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"964.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00054\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.126\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00212\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-61.0\", \"ZT\": \"0.05\", \"formula\": \"Mg1.9Ca0.1Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.2\", \"Average atomic mass (g/mol)\": \"26.09\", \"Scarcity (wt fraction/abundance)\": \"26.71\", \"HHI (production)\": \"4990.0\", \"HHI (reserves)\": \"730.6\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"472.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000176\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3720.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.066\"}, {\"doi\": \"10.1016/j.jcrysgro.2006.10.270\", \"Electrical resistivity (\\u03a9cm)\": \"0.00122\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-178.0\", \"ZT\": \"0.78\", \"formula\": \"Mg2Si1\", \"comment\": \"\", \"synthesis\": \"Bridgman method, Ar-H gas\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Akasaka 2007\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 2.341182266, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"7.25\", \"Average atomic mass (g/mol)\": \"25.57\", \"Scarcity (wt fraction/abundance)\": \"27.34\", \"HHI (production)\": \"5057.0\", \"HHI (reserves)\": \"683.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"821.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0026\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.083\"}, {\"doi\": \"10.1038/nmat3273\", \"Electrical resistivity (\\u03a9cm)\": \"0.001\", \"Seebeck coefficient (\\u03bcCV/K)\": \"90.0\", \"ZT\": \"0.24\", \"formula\": \"Cu2Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 0.729, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.97\", \"Average atomic mass (g/mol)\": \"68.68\", \"Scarcity (wt fraction/abundance)\": \"7674000.0\", \"HHI (production)\": \"1825.0\", \"HHI (reserves)\": \"1672.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00081\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.755\"}, {\"doi\": \"10.1038/nmat3277\", \"Electrical resistivity (\\u03a9cm)\": \"0.000605\", \"Seebeck coefficient (\\u03bcCV/K)\": \"62.0\", \"ZT\": \"0.19\", \"formula\": \"Cu1.98Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 0.5792370248, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.25\", \"Average atomic mass (g/mol)\": \"68.72\", \"Scarcity (wt fraction/abundance)\": \"7721000.0\", \"HHI (production)\": \"1826.0\", \"HHI (reserves)\": \"1673.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1650.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000644\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3890.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.968\"}, {\"doi\": \"http://link.aip.org/link/doi/10.1063/1.1562337\", \"Electrical resistivity (\\u03a9cm)\": \"0.00197\", \"Seebeck coefficient (\\u03bcCV/K)\": \"126.0\", \"ZT\": \"0.24\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"flux (SrCl2), air\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Shikano 2003\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.7191894977, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"3.51\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"507.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000799\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.106\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"117.0\", \"ZT\": \"0.04\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"93.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000128\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.034\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00813\", \"Seebeck coefficient (\\u03bcCV/K)\": \"117.0\", \"ZT\": \"0.05\", \"formula\": \"Ca2.7Na0.3Co4O9\", \"comment\": \"*extrapolated from 323 K, kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"30.93\", \"Scarcity (wt fraction/abundance)\": \"17330.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1745.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"123.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000168\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.045\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"135.0\", \"ZT\": \"0.05\", \"formula\": \"Ca2.7Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"34.41\", \"Scarcity (wt fraction/abundance)\": \"6713000.0\", \"HHI (production)\": \"2799.0\", \"HHI (reserves)\": \"2245.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"96.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000177\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.035\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00936\", \"Seebeck coefficient (\\u03bcCV/K)\": \"132.0\", \"ZT\": \"0.06\", \"formula\": \"Ca2.4Na0.3Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"34.09\", \"Scarcity (wt fraction/abundance)\": \"6776000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2239.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"107.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000186\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.039\"}, {\"doi\": \"http://jjap.jsap.jp/link?JJAP/43/L540/\", \"Electrical resistivity (\\u03a9cm)\": \"0.000878\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-92.0\", \"ZT\": \"0.29\", \"formula\": \"Sr0.9Y0.1Ti1O3\", \"comment\": \"Unit Cell = (Sr0.905 Y0.07) (Ti0.995 O3)\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Obara 2004\", \"Structure\": \"ICSD #181231, 300K\", \"marker\": \"{'radius': 0.8770643508, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"7.0\", \"Average atomic mass (g/mol)\": \"36.72\", \"Scarcity (wt fraction/abundance)\": \"2782.0\", \"HHI (production)\": \"2693.0\", \"HHI (reserves)\": \"1952.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.872\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1140.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000975\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8560.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.119\"}, {\"doi\": \"10.1016/j.jallcom.2003.07.016\", \"Electrical resistivity (\\u03a9cm)\": \"0.000494\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-82.0\", \"ZT\": \"0.41\", \"formula\": \"Ba0.3Sr0.6La0.1Ti1O3\", \"comment\": \"*extrapolated from 330 K\", \"synthesis\": \"solid state reaction , Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2004\", \"Structure\": \"ICSD #181231, 300K\", \"marker\": \"{'radius': 1.231751266, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.07\", \"Average atomic mass (g/mol)\": \"40.7\", \"Scarcity (wt fraction/abundance)\": \"3096.0\", \"HHI (production)\": \"2709.0\", \"HHI (reserves)\": \"1946.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.872\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2030.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00137\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6760.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.364\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.587\", \"Seebeck coefficient (\\u03bcCV/K)\": \"295.0\", \"ZT\": \"0.00444\", \"formula\": \"Cu1Rh1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.61\", \"Scarcity (wt fraction/abundance)\": \"518600000.0\", \"HHI (production)\": \"2265.0\", \"HHI (reserves)\": \"4717.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1.704\", \"Power Factor (W/(K\\u00b2m))\": \"1.48e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"86900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.131\", \"Seebeck coefficient (\\u03bcCV/K)\": \"261.0\", \"ZT\": \"0.02\", \"formula\": \"Cu1Rh0.99Mg0.01O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.42\", \"Scarcity (wt fraction/abundance)\": \"515400000.0\", \"HHI (production)\": \"2263.0\", \"HHI (reserves)\": \"4695.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"7.61\", \"Power Factor (W/(K\\u00b2m))\": \"5.18e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"68100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"174.0\", \"ZT\": \"0.08\", \"formula\": \"Cu1Rh0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.83\", \"Scarcity (wt fraction/abundance)\": \"505800000.0\", \"HHI (production)\": \"2259.0\", \"HHI (reserves)\": \"4627.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"90.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.000277\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.00164\", \"Seebeck coefficient (\\u03bcCV/K)\": \"100.0\", \"ZT\": \"0.18\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.5454927439, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"610.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000606\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9940.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"1.199\", \"Seebeck coefficient (\\u03bcCV/K)\": \"165.0\", \"ZT\": \"0.000681\", \"formula\": \"Ca3Al1Sb3\", \"comment\": \"*seebeck extrapolated from 333 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.45\", \"Average atomic mass (g/mol)\": \"73.21\", \"Scarcity (wt fraction/abundance)\": \"3564000.0\", \"HHI (production)\": \"6623.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.834\", \"Power Factor (W/(K\\u00b2m))\": \"2.27e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000421\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.098\", \"Seebeck coefficient (\\u03bcCV/K)\": \"90.0\", \"ZT\": \"0.00248\", \"formula\": \"Ca2.97Na0.03Al1Sb3\", \"comment\": \"*seebeck extrapolated from 333 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.67\", \"Average atomic mass (g/mol)\": \"73.14\", \"Scarcity (wt fraction/abundance)\": \"3567000.0\", \"HHI (production)\": \"6622.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"10.2\", \"Power Factor (W/(K\\u00b2m))\": \"8.26e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00447\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.059\", \"Seebeck coefficient (\\u03bcCV/K)\": \"82.0\", \"ZT\": \"0.00338\", \"formula\": \"Ca2.94Na0.06Al1Sb3\", \"comment\": \"*seebeck extrapolated from 333 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.65\", \"Average atomic mass (g/mol)\": \"73.07\", \"Scarcity (wt fraction/abundance)\": \"3571000.0\", \"HHI (production)\": \"6621.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"17.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.13e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6640.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00753\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"113.0\", \"ZT\": \"0.01\", \"formula\": \"Ca2.85Na0.15Al1Sb3\", \"comment\": \"*seebeck extrapolated from 333 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.59\", \"Average atomic mass (g/mol)\": \"72.85\", \"Scarcity (wt fraction/abundance)\": \"3582000.0\", \"HHI (production)\": \"6618.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"36.4\", \"Power Factor (W/(K\\u00b2m))\": \"4.61e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.017\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.048\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-191.0\", \"ZT\": \"0.02\", \"formula\": \"Fe0.998Co0.002Si2\", \"comment\": \"*extrapolated from 315 K\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.69\", \"Average atomic mass (g/mol)\": \"37.34\", \"Scarcity (wt fraction/abundance)\": \"48.87\", \"HHI (production)\": \"3570.0\", \"HHI (reserves)\": \"1187.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.1\", \"Power Factor (W/(K\\u00b2m))\": \"7.68e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00271\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.128\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-318.0\", \"ZT\": \"0.02\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.04O0.06\", \"comment\": \"*extrapolated from 315 K\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.59\", \"Average atomic mass (g/mol)\": \"37.6\", \"Scarcity (wt fraction/abundance)\": \"1051.0\", \"HHI (production)\": \"3739.0\", \"HHI (reserves)\": \"1227.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"7.843\", \"Power Factor (W/(K\\u00b2m))\": \"7.93e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"101000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00125\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.27\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-226.0\", \"ZT\": \"0.00568\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.12O0.18\", \"comment\": \"*extrapolated from 315 K\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.86\", \"Average atomic mass (g/mol)\": \"38.06\", \"Scarcity (wt fraction/abundance)\": \"2834.0\", \"HHI (production)\": \"4040.0\", \"HHI (reserves)\": \"1297.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.704\", \"Power Factor (W/(K\\u00b2m))\": \"1.89e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"51100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000948\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.457\", \"Seebeck coefficient (\\u03bcCV/K)\": \"470.0\", \"ZT\": \"0.01\", \"formula\": \"Ca5Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.54\", \"Average atomic mass (g/mol)\": \"75.76\", \"Scarcity (wt fraction/abundance)\": \"3709000.0\", \"HHI (production)\": \"6736.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.188\", \"Power Factor (W/(K\\u00b2m))\": \"4.83e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"221000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00104\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.033\", \"Seebeck coefficient (\\u03bcCV/K)\": \"193.0\", \"ZT\": \"0.03\", \"formula\": \"Ca4.95Na0.05Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.49\", \"Average atomic mass (g/mol)\": \"75.7\", \"Scarcity (wt fraction/abundance)\": \"3712000.0\", \"HHI (production)\": \"6735.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"30.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000112\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"37200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.015\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.00506\", \"Seebeck coefficient (\\u03bcCV/K)\": \"143.0\", \"ZT\": \"0.12\", \"formula\": \"Ca4.75Na0.25Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.3621929051, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.45\", \"Average atomic mass (g/mol)\": \"75.43\", \"Scarcity (wt fraction/abundance)\": \"3725000.0\", \"HHI (production)\": \"6732.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"198.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000402\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.1\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.888\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-413.0\", \"ZT\": \"0.00577\", \"formula\": \"Fe1.98Ti0.02O3\", \"comment\": \"Unit Cell = (Fe1.831 Ti0.169) O3\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.91\", \"Scarcity (wt fraction/abundance)\": \"13.87\", \"HHI (production)\": \"1837.0\", \"HHI (reserves)\": \"1111.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"11300.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.92e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"171000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.376\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-366.0\", \"ZT\": \"0.01\", \"formula\": \"Fe1.96Ti0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"7.82\", \"Average atomic mass (g/mol)\": \"31.87\", \"Scarcity (wt fraction/abundance)\": \"14.74\", \"HHI (production)\": \"1829.0\", \"HHI (reserves)\": \"1112.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"26600.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.57e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"134000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"2.487\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.412\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-335.0\", \"ZT\": \"0.00818\", \"formula\": \"Fe1.94Ti0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.39\", \"Average atomic mass (g/mol)\": \"31.84\", \"Scarcity (wt fraction/abundance)\": \"15.62\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"1113.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24300.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.73e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"112000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"2.784\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"1.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-428.0\", \"ZT\": \"0.00549\", \"formula\": \"Fe1.98Sn0.02O3\", \"comment\": \"Unit Cell = Fe1.874 Sn0.096 O3\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.19\", \"Scarcity (wt fraction/abundance)\": \"6569.0\", \"HHI (production)\": \"1853.0\", \"HHI (reserves)\": \"1117.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"10000.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.83e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"183000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.467\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-364.0\", \"ZT\": \"0.00853\", \"formula\": \"Fe1.96Sn0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.84\", \"Average atomic mass (g/mol)\": \"32.44\", \"Scarcity (wt fraction/abundance)\": \"13020.0\", \"HHI (production)\": \"1860.0\", \"HHI (reserves)\": \"1122.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21400.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.84e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"133000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"2.289\"}, {\"doi\": \"10.1016/j.jssc.2011.02.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.000588\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-27.0\", \"ZT\": \"0.04\", \"formula\": \"Ba7Sr1Al16Si30\", \"comment\": \"\", \"synthesis\": \"flux (Al), dynamic vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Roudebush 2011\", \"Structure\": \"ICSD #380509, 90K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.31\", \"Average atomic mass (g/mol)\": \"43.02\", \"Scarcity (wt fraction/abundance)\": \"1088.0\", \"HHI (production)\": \"3387.0\", \"HHI (reserves)\": \"1633.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1193.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.691\", \"Atoms per unit cell\": \"55.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1700.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00012\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"703.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.539\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"2.919\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-752.0\", \"ZT\": \"0.00582\", \"formula\": \"Nd2Cu1O4\", \"comment\": \"*Seebeck extrapolated from 700K, kappa extrapolated from 850 K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"29.6\", \"Average atomic mass (g/mol)\": \"59.43\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6889.0\", \"HHI (reserves)\": \"2479.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.343\", \"Power Factor (W/(K\\u00b2m))\": \"1.94e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"566000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"8.47e-06\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.059\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-249.0\", \"ZT\": \"0.03\", \"formula\": \"Nd2Cu0.98Ni0.02O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"9.811\", \"Average atomic mass (g/mol)\": \"59.42\", \"Scarcity (wt fraction/abundance)\": \"20980.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2480.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"16.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000105\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"62200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00126\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.19\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-343.0\", \"ZT\": \"0.02\", \"formula\": \"Nd2Cu0.98Zn0.02O4\", \"comment\": \"*Seebeck extrapolated from 700K, kappa extrapolated from 850 K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"17.1\", \"Average atomic mass (g/mol)\": \"59.44\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2481.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5.269\", \"Power Factor (W/(K\\u00b2m))\": \"6.21e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"118000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000226\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00053\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-45.0\", \"ZT\": \"0.11\", \"formula\": \"La3Te3.8Sb0.2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.3438679245, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.402\", \"Average atomic mass (g/mol)\": \"132.28\", \"Scarcity (wt fraction/abundance)\": \"523800000.0\", \"HHI (production)\": \"5987.0\", \"HHI (reserves)\": \"4082.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1890.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000382\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2020.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.575\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.0011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-53.0\", \"ZT\": \"0.08\", \"formula\": \"La3Te3.65Sb0.35\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.05\", \"Average atomic mass (g/mol)\": \"132.15\", \"Scarcity (wt fraction/abundance)\": \"503700000.0\", \"HHI (production)\": \"6089.0\", \"HHI (reserves)\": \"4051.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"909.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000255\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2810.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.325\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-91.0\", \"ZT\": \"0.01\", \"formula\": \"La3Te3.35Sb0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.47\", \"Average atomic mass (g/mol)\": \"131.9\", \"Scarcity (wt fraction/abundance)\": \"463400000.0\", \"HHI (production)\": \"6293.0\", \"HHI (reserves)\": \"3990.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"55.6\", \"Power Factor (W/(K\\u00b2m))\": \"4.6e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8280.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.028\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.0071\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-71.0\", \"ZT\": \"0.02\", \"formula\": \"La3Te3.35Bi0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.967\", \"Average atomic mass (g/mol)\": \"140.0\", \"Scarcity (wt fraction/abundance)\": \"444300000.0\", \"HHI (production)\": \"6025.0\", \"HHI (reserves)\": \"4313.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"141.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.1e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5040.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.052\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00061\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-41.0\", \"ZT\": \"0.08\", \"formula\": \"La2.99Te4\", \"comment\": \"*kappa extrapolated from  375 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.46\", \"Average atomic mass (g/mol)\": \"132.44\", \"Scarcity (wt fraction/abundance)\": \"551400000.0\", \"HHI (production)\": \"5846.0\", \"HHI (reserves)\": \"4124.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1640.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000274\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1670.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.488\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.0027\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-41.0\", \"ZT\": \"0.02\", \"formula\": \"La2.74Te4\", \"comment\": \"*kappa extrapolated from  375 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.24\", \"Average atomic mass (g/mol)\": \"132.2\", \"Scarcity (wt fraction/abundance)\": \"572900000.0\", \"HHI (production)\": \"5704.0\", \"HHI (reserves)\": \"4163.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"370.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.23e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1680.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.219\"}, {\"doi\": \"10.1021/nl202439h\", \"Electrical resistivity (\\u03a9cm)\": \"0.297\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-210.0\", \"ZT\": \"0.00446\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"microwave solvothermal, air\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Jood 2011\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.78\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.37\", \"Power Factor (W/(K\\u00b2m))\": \"1.49e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000887\"}, {\"doi\": \"10.1063/1.3291563\", \"Electrical resistivity (\\u03a9cm)\": \"0.00283\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-92.0\", \"ZT\": \"0.09\", \"formula\": \"Sr0.61Ba0.39Nb2O6\", \"comment\": \"*kappa from Choy 1992 polycrystalline samples used, values parallel to c axis\", \"synthesis\": \"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Lee 2010\", \"Structure\": \"ICSD #96013, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"1.667\", \"Average atomic mass (g/mol)\": \"43.2\", \"Scarcity (wt fraction/abundance)\": \"26540.0\", \"HHI (production)\": \"5182.0\", \"HHI (reserves)\": \"5061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"610.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.564\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"354.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000302\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8540.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.155\"}, {\"doi\": \"10.1063/1.3291563\", \"Electrical resistivity (\\u03a9cm)\": \"0.105\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-186.0\", \"ZT\": \"0.00988\", \"formula\": \"Sr0.61Ba0.39Nb2O6\", \"comment\": \"*kappa from Choy 1992 polycrystalline samples used, values parallel to c axis\", \"synthesis\": \"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Lee 2010\", \"Structure\": \"ICSD #96013, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"1.667\", \"Average atomic mass (g/mol)\": \"43.2\", \"Scarcity (wt fraction/abundance)\": \"26540.0\", \"HHI (production)\": \"5182.0\", \"HHI (reserves)\": \"5061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"610.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.564\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.522\", \"Power Factor (W/(K\\u00b2m))\": \"3.29e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00418\"}, {\"doi\": \"10.1557/jmr.2010.78\", \"Electrical resistivity (\\u03a9cm)\": \"0.062\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-220.0\", \"ZT\": \"0.02\", \"formula\": \"Sr0.61Ba0.39Nb2O6\", \"comment\": \"*kappa from Choy 1992 polycrystalline samples used, values parallel to c axis\", \"synthesis\": \"templated grain growth, air, anneal PO<sub>2</sub> 10<sup>-14</sup>\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Lee 2011\", \"Structure\": \"ICSD #96013, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"1.667\", \"Average atomic mass (g/mol)\": \"43.2\", \"Scarcity (wt fraction/abundance)\": \"26540.0\", \"HHI (production)\": \"5182.0\", \"HHI (reserves)\": \"5061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"610.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.564\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"16.2\", \"Power Factor (W/(K\\u00b2m))\": \"7.82e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0071\"}, {\"doi\": \"10.1111/j.1551-2916.2012.05169.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.00114\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-19.0\", \"ZT\": \"0.0095\", \"formula\": \"Sr4.5Nb4.5O15.5\", \"comment\": \"\", \"synthesis\": \"floating zone method, Ar\", \"form\": \"single crystal\", \"temperature\": \"300\", \"author\": \"Sakai 2012\", \"Structure\": \"ICSD #48207, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.45\", \"Average atomic mass (g/mol)\": \"43.28\", \"Scarcity (wt fraction/abundance)\": \"22330.0\", \"HHI (production)\": \"5032.0\", \"HHI (reserves)\": \"4699.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"735.99\", \"Average atomic volume (\\u212b\\u00b3)\": \"14.154\", \"Atoms per unit cell\": \"52.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"877.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.17e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"361.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.262\"}, {\"doi\": \"10.1111/j.1551-2916.2012.05169.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.005\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-107.0\", \"ZT\": \"0.07\", \"formula\": \"Sr1.6La0.4Nb2O7\", \"comment\": \"\", \"synthesis\": \"floating zone method, Ar\", \"form\": \"single\", \"temperature\": \"300\", \"author\": \"Sakai 2012\", \"Structure\": \"ICSD #187, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"1.8\", \"Average atomic mass (g/mol)\": \"44.87\", \"Scarcity (wt fraction/abundance)\": \"24210.0\", \"HHI (production)\": \"5577.0\", \"HHI (reserves)\": \"4628.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"597.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"44.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000229\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.081\"}, {\"doi\": \"10.1021/nl8026795\", \"Electrical resistivity (\\u03a9cm)\": \"0.00118\", \"Seebeck coefficient (\\u03bcCV/K)\": \"121.0\", \"ZT\": \"0.37\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"ball milling, hot-pressed nanopowders\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Joshi 2008\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.1136635004, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"2.449\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"849.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00124\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.254\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.000679\", \"Seebeck coefficient (\\u03bcCV/K)\": \"81.0\", \"ZT\": \"0.29\", \"formula\": \"Pb0.96Sr0.4Te1Na0.2\", \"comment\": \"\", \"synthesis\": \"sparks plasma sintering\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 0.86979177, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.85\", \"Average atomic mass (g/mol)\": \"143.03\", \"Scarcity (wt fraction/abundance)\": \"348500000.0\", \"HHI (production)\": \"2897.0\", \"HHI (reserves)\": \"2980.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1470.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000966\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6560.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.378\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.00041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"68.0\", \"ZT\": \"0.34\", \"formula\": \"Pb0.98Sr0.2Te1Na0.1\", \"comment\": \"\", \"synthesis\": \"melting\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 1.01626272, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.065\", \"Average atomic mass (g/mol)\": \"153.72\", \"Scarcity (wt fraction/abundance)\": \"364100000.0\", \"HHI (production)\": \"2843.0\", \"HHI (reserves)\": \"2981.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2440.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00113\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.583\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.000417\", \"Seebeck coefficient (\\u03bcCV/K)\": \"64.0\", \"ZT\": \"0.29\", \"formula\": \"Pb0.98Te1Na0.2\", \"comment\": \"\", \"synthesis\": \"melting\", \"form\": \"polycrystalline\", \"temperature\": \"300\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 0.88436736, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"4.29\", \"Average atomic mass (g/mol)\": \"153.79\", \"Scarcity (wt fraction/abundance)\": \"380700000.0\", \"HHI (production)\": \"2761.0\", \"HHI (reserves)\": \"2963.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2400.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000983\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.409\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"50.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-463.0\", \"ZT\": \"0.000171\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.02\", \"Power Factor (W/(K\\u00b2m))\": \"4.29e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"214000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.046\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-202.0\", \"ZT\": \"0.04\", \"formula\": \"Ca0.98La0.02Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82210, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.0\", \"Scarcity (wt fraction/abundance)\": \"917.3\", \"HHI (production)\": \"1996.0\", \"HHI (reserves)\": \"1310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.74\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.387\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.7\", \"Power Factor (W/(K\\u00b2m))\": \"8.82e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-124.0\", \"ZT\": \"0.04\", \"formula\": \"Ca0.96La0.04Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82209, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.39\", \"Scarcity (wt fraction/abundance)\": \"1423.0\", \"HHI (production)\": \"2128.0\", \"HHI (reserves)\": \"1343.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.49\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.424\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"65.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.0001\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-104.0\", \"ZT\": \"0.04\", \"formula\": \"Ca0.94La0.06Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82208, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.79\", \"Scarcity (wt fraction/abundance)\": \"1915.0\", \"HHI (production)\": \"2255.0\", \"HHI (reserves)\": \"1376.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.24\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.462\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"82.2\", \"Power Factor (W/(K\\u00b2m))\": \"8.84e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.00997\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.92La0.08Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82207, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"2394.0\", \"HHI (production)\": \"2380.0\", \"HHI (reserves)\": \"1407.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.497\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"100.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.95e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6930.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"28.9\", \"Seebeck coefficient (\\u03bcCV/K)\": \"295.0\", \"ZT\": \"0.000121\", \"formula\": \"Li0.0024Ni0.9976O1\", \"comment\": \"Data at 460 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"16.172\", \"Average atomic mass (g/mol)\": \"37.28\", \"Scarcity (wt fraction/abundance)\": \"6484.0\", \"HHI (production)\": \"883.7\", \"HHI (reserves)\": \"1270.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.035\", \"Power Factor (W/(K\\u00b2m))\": \"3.01e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"87000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"2.09e-06\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"5.086\", \"Seebeck coefficient (\\u03bcCV/K)\": \"249.0\", \"ZT\": \"0.000489\", \"formula\": \"Li0.0066Ni0.9944O1\", \"comment\": \"Data at 460 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"8.328\", \"Average atomic mass (g/mol)\": \"37.19\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"884.2\", \"HHI (reserves)\": \"1270.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.197\", \"Power Factor (W/(K\\u00b2m))\": \"1.22e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"62200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"2.3e-05\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.064\", \"Seebeck coefficient (\\u03bcCV/K)\": \"117.0\", \"ZT\": \"0.00851\", \"formula\": \"Li0.0184Ni0.9816O1\", \"comment\": \"Data at 460 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"36.87\", \"Scarcity (wt fraction/abundance)\": \"6533.0\", \"HHI (production)\": \"885.3\", \"HHI (reserves)\": \"1271.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"15.6\", \"Power Factor (W/(K\\u00b2m))\": \"2.13e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"103.0\", \"ZT\": \"0.03\", \"formula\": \"Li0.0242Ni0.9758O1\", \"comment\": \"Data at 460 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.751\", \"Average atomic mass (g/mol)\": \"36.72\", \"Scarcity (wt fraction/abundance)\": \"6552.0\", \"HHI (production)\": \"885.9\", \"HHI (reserves)\": \"1272.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"81.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.53e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.021\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"2.925\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-549.0\", \"ZT\": \"0.00412\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.306\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.342\", \"Power Factor (W/(K\\u00b2m))\": \"1.03e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"302000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000101\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-119.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.98Bi0.02Mn0.98Nb0.02O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.275\", \"Average atomic mass (g/mol)\": \"29.43\", \"Scarcity (wt fraction/abundance)\": \"1672000.0\", \"HHI (production)\": \"2034.0\", \"HHI (reserves)\": \"1500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.4\", \"Power Factor (W/(K\\u00b2m))\": \"6.6e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.02\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.00982\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-114.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.96Bi0.04Mn0.96Nb0.04O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.16\", \"Average atomic mass (g/mol)\": \"30.26\", \"Scarcity (wt fraction/abundance)\": \"3252000.0\", \"HHI (production)\": \"2198.0\", \"HHI (reserves)\": \"1711.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"102.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000133\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.046\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.00726\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-72.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9Bi0.1Mn0.9Nb0.1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.74\", \"Scarcity (wt fraction/abundance)\": \"7513000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"2282.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"138.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.23e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5250.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/jmr.2011.140\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-204.0\", \"ZT\": \"0.08\", \"formula\": \"Ca1Mn0.98Nb0.02O3\", \"comment\": \"\", \"synthesis\": \"Ultrasonic Spray Pyrolysis\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Populoh 2011\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.075\", \"Average atomic mass (g/mol)\": \"28.75\", \"Scarcity (wt fraction/abundance)\": \"1087.0\", \"HHI (production)\": \"1950.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000193\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"41600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.022\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-154.0\", \"ZT\": \"0.05\", \"formula\": \"Ca1Mn0.98Ru0.02O3\", \"comment\": \"Seebeck extrapolated from 500 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.79\", \"Scarcity (wt fraction/abundance)\": \"14040000.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"1366.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"54.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000129\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00752\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-120.0\", \"ZT\": \"0.08\", \"formula\": \"Ca1Mn0.96Ru0.04O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.758\", \"Average atomic mass (g/mol)\": \"28.97\", \"Scarcity (wt fraction/abundance)\": \"27910000.0\", \"HHI (production)\": \"1904.0\", \"HHI (reserves)\": \"1456.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"133.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000191\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.035\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.0066\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-102.0\", \"ZT\": \"0.06\", \"formula\": \"Ca1Mn0.94Ru0.06O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.16\", \"Scarcity (wt fraction/abundance)\": \"41600000.0\", \"HHI (production)\": \"1925.0\", \"HHI (reserves)\": \"1544.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"151.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000156\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00396\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-61.0\", \"ZT\": \"0.04\", \"formula\": \"Ca1Mn0.9Ru0.1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.53\", \"Scarcity (wt fraction/abundance)\": \"68460000.0\", \"HHI (production)\": \"1966.0\", \"HHI (reserves)\": \"1717.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"253.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.27e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3670.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00311\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-36.0\", \"ZT\": \"0.02\", \"formula\": \"Ca1Mn0.82Ru0.18O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.26\", \"Scarcity (wt fraction/abundance)\": \"120200000.0\", \"HHI (production)\": \"2045.0\", \"HHI (reserves)\": \"2051.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"322.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.1e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1270.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-215.0\", \"ZT\": \"0.07\", \"formula\": \"Ca1Gd0.98Mn0.02O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.66\", \"Scarcity (wt fraction/abundance)\": \"111100.0\", \"HHI (production)\": \"6744.0\", \"HHI (reserves)\": \"2336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"36.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000168\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"46400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-164.0\", \"ZT\": \"0.08\", \"formula\": \"Ca1Gd0.96Mn0.04O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.615\", \"Average atomic mass (g/mol)\": \"48.25\", \"Scarcity (wt fraction/abundance)\": \"109800.0\", \"HHI (production)\": \"6685.0\", \"HHI (reserves)\": \"2323.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"77.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000208\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.047\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-119.0\", \"ZT\": \"0.05\", \"formula\": \"Ca1Gd0.94Mn0.06O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.57\", \"Average atomic mass (g/mol)\": \"47.84\", \"Scarcity (wt fraction/abundance)\": \"108400.0\", \"HHI (production)\": \"6625.0\", \"HHI (reserves)\": \"2310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"88.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000124\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.033\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00176\", \"Seebeck coefficient (\\u03bcCV/K)\": \"23.0\", \"ZT\": \"0.01\", \"formula\": \"Nd1.4Bi0.6Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78129, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"58.31\", \"Scarcity (wt fraction/abundance)\": \"326600000.0\", \"HHI (production)\": \"5126.0\", \"HHI (reserves)\": \"4765.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1102.66\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.53\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"569.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.03e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"533.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00117\", \"Seebeck coefficient (\\u03bcCV/K)\": \"21.0\", \"ZT\": \"0.02\", \"formula\": \"Nd1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"60.67\", \"Scarcity (wt fraction/abundance)\": \"321300000.0\", \"HHI (production)\": \"4772.0\", \"HHI (reserves)\": \"5060.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"854.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.83e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"448.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00322\", \"Seebeck coefficient (\\u03bcCV/K)\": \"18.0\", \"ZT\": \"0.0039\", \"formula\": \"Yb1.4Bi0.6Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"61.98\", \"Scarcity (wt fraction/abundance)\": \"307400000.0\", \"HHI (production)\": \"5384.0\", \"HHI (reserves)\": \"4668.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"311.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.75e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"314.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00169\", \"Seebeck coefficient (\\u03bcCV/K)\": \"19.0\", \"ZT\": \"0.0088\", \"formula\": \"Yb1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"63.29\", \"Scarcity (wt fraction/abundance)\": \"308100000.0\", \"HHI (production)\": \"4966.0\", \"HHI (reserves)\": \"4980.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"591.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.2e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"372.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000491\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-2.0\", \"ZT\": \"0.000218\", \"formula\": \"Bi2Ru2O7\", \"comment\": \"Extrapolated from 478 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73787, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"66.55\", \"Scarcity (wt fraction/abundance)\": \"309700000.0\", \"HHI (production)\": \"3994.0\", \"HHI (reserves)\": \"5707.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1090.63\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.394\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1880.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.46e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2.681\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00101\", \"Seebeck coefficient (\\u03bcCV/K)\": \"21.0\", \"ZT\": \"0.02\", \"formula\": \"Y0.5Bi1.5Ru2O7\", \"comment\": \"Extrapolated from 478 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73790, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"61.1\", \"Scarcity (wt fraction/abundance)\": \"328200000.0\", \"HHI (production)\": \"4178.0\", \"HHI (reserves)\": \"5460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1079.79\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.27\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"969.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.55e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"461.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.002\", \"Seebeck coefficient (\\u03bcCV/K)\": \"15.0\", \"ZT\": \"0.00478\", \"formula\": \"Y1Bi1Ru2O7\", \"comment\": \"Extrapolated from 478 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73793, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.64\", \"Scarcity (wt fraction/abundance)\": \"350400000.0\", \"HHI (production)\": \"4398.0\", \"HHI (reserves)\": \"5165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1069.75\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.156\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"502.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.2e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"238.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"5.732\", \"Seebeck coefficient (\\u03bcCV/K)\": \"270.0\", \"ZT\": \"0.000509\", \"formula\": \"Y2Ru2O7\", \"comment\": \"Extrapolated from 478 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73799, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"44.72\", \"Scarcity (wt fraction/abundance)\": \"410900000.0\", \"HHI (production)\": \"4999.0\", \"HHI (reserves)\": \"4357.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1040.8\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.827\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.173\", \"Power Factor (W/(K\\u00b2m))\": \"1.27e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"72900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-90.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9Nd0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164747, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.413\", \"Average atomic mass (g/mol)\": \"30.69\", \"Scarcity (wt fraction/abundance)\": \"2894.0\", \"HHI (production)\": \"2525.0\", \"HHI (reserves)\": \"1444.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.546\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"83.8\", \"Power Factor (W/(K\\u00b2m))\": \"6.83e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8150.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.034\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-90.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9Tb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164751, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.587\", \"Average atomic mass (g/mol)\": \"30.98\", \"Scarcity (wt fraction/abundance)\": \"96250.0\", \"HHI (production)\": \"2591.0\", \"HHI (reserves)\": \"1460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.451\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"93.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.58e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8150.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.057\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.00698\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-90.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.9Ho0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164753, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.068\", \"Average atomic mass (g/mol)\": \"31.1\", \"Scarcity (wt fraction/abundance)\": \"85220.0\", \"HHI (production)\": \"2618.0\", \"HHI (reserves)\": \"1467.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.422\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"143.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000117\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8150.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.068\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.00406\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-90.0\", \"ZT\": \"0.08\", \"formula\": \"Ca0.9Yb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.639\", \"Average atomic mass (g/mol)\": \"31.26\", \"Scarcity (wt fraction/abundance)\": \"37270.0\", \"HHI (production)\": \"2653.0\", \"HHI (reserves)\": \"1475.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"247.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000201\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8150.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.147\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.461\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-600.0\", \"ZT\": \"0.03\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.973\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.169\", \"Power Factor (W/(K\\u00b2m))\": \"7.81e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"360000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000712\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00639\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-94.0\", \"ZT\": \"0.06\", \"formula\": \"Ca0.9Tb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69824, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.571\", \"Average atomic mass (g/mol)\": \"30.98\", \"Scarcity (wt fraction/abundance)\": \"96250.0\", \"HHI (production)\": \"2591.0\", \"HHI (reserves)\": \"1460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.479\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"157.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000138\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.097\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.0055\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-44.0\", \"ZT\": \"0.01\", \"formula\": \"Ca0.7Tb0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69826, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.466\", \"Average atomic mass (g/mol)\": \"35.73\", \"Scarcity (wt fraction/abundance)\": \"249700.0\", \"HHI (production)\": \"3759.0\", \"HHI (reserves)\": \"1755.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.15\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.658\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"182.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.58e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1970.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.121\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.0074\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-82.0\", \"ZT\": \"0.04\", \"formula\": \"Ca0.9Ho0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160306, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.546\", \"Average atomic mass (g/mol)\": \"31.1\", \"Scarcity (wt fraction/abundance)\": \"85220.0\", \"HHI (production)\": \"2618.0\", \"HHI (reserves)\": \"1467.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.04\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.452\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"135.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.04e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6690.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.085\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.0044\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-45.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.7Ho0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.524\", \"Average atomic mass (g/mol)\": \"36.09\", \"Scarcity (wt fraction/abundance)\": \"219600.0\", \"HHI (production)\": \"3816.0\", \"HHI (reserves)\": \"1769.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"228.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.62e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2030.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.146\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00478\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-82.0\", \"ZT\": \"0.06\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.482\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"209.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00014\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6680.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.138\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00649\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-42.0\", \"ZT\": \"0.01\", \"formula\": \"Ca0.7Y0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #97601, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.467\", \"Average atomic mass (g/mol)\": \"31.53\", \"Scarcity (wt fraction/abundance)\": \"5816.0\", \"HHI (production)\": \"3058.0\", \"HHI (reserves)\": \"1490.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"219.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.992\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"154.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.67e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1730.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.102\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000509\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-32.0\", \"ZT\": \"0.08\", \"formula\": \"Ba1Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.156\", \"Average atomic mass (g/mol)\": \"78.5\", \"Scarcity (wt fraction/abundance)\": \"44820.0\", \"HHI (production)\": \"2535.0\", \"HHI (reserves)\": \"1822.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1960.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000201\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1020.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.461\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000476\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-30.0\", \"ZT\": \"0.08\", \"formula\": \"Ba0.8Sr0.2Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.306\", \"Average atomic mass (g/mol)\": \"76.52\", \"Scarcity (wt fraction/abundance)\": \"45940.0\", \"HHI (production)\": \"2579.0\", \"HHI (reserves)\": \"1839.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2100.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000193\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"917.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.62\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.00127\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-51.0\", \"ZT\": \"0.08\", \"formula\": \"Ba0.6Sr0.4Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151609, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.364\", \"Average atomic mass (g/mol)\": \"74.53\", \"Scarcity (wt fraction/abundance)\": \"47120.0\", \"HHI (production)\": \"2625.0\", \"HHI (reserves)\": \"1856.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"301.96\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.098\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"786.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000207\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2640.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.325\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.00395\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-96.0\", \"ZT\": \"0.09\", \"formula\": \"Ba0.4Sr0.6Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151609, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.133\", \"Average atomic mass (g/mol)\": \"72.54\", \"Scarcity (wt fraction/abundance)\": \"48360.0\", \"HHI (production)\": \"2674.0\", \"HHI (reserves)\": \"1874.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"301.96\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.098\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"253.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000235\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.116\"}, {\"doi\": \"10.1557/PROC-793-S3.3\", \"Electrical resistivity (\\u03a9cm)\": \"0.00284\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-20.0\", \"ZT\": \"0.00556\", \"formula\": \"La1Ni1O3\", \"comment\": \"\", \"synthesis\": \"Evaporate nitrates (1173 K, air)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Funahashi 2003\", \"Structure\": \"ICSD #84933, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.12\", \"Scarcity (wt fraction/abundance)\": \"17470.0\", \"HHI (production)\": \"5693.0\", \"HHI (reserves)\": \"2221.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"339.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.314\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"352.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.39e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"395.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/PROC-793-S3.3\", \"Electrical resistivity (\\u03a9cm)\": \"0.00267\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-21.0\", \"ZT\": \"0.00657\", \"formula\": \"La0.9Bi0.1Ni1O3\", \"comment\": \"\", \"synthesis\": \"Evaporate nitrates (1173 K, air)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Funahashi 2003\", \"Structure\": \"ICSD #84933, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"50.52\", \"Scarcity (wt fraction/abundance)\": \"4882000.0\", \"HHI (production)\": \"5452.0\", \"HHI (reserves)\": \"2483.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"339.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.314\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"374.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.64e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"439.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.2007.4569450\", \"Electrical resistivity (\\u03a9cm)\": \"0.00604\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-139.0\", \"ZT\": \"0.13\", \"formula\": \"Ca0.96Sm0.04Mn1O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sanmathi 2007\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.3866212881, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.48\", \"Scarcity (wt fraction/abundance)\": \"6638.0\", \"HHI (production)\": \"2150.0\", \"HHI (reserves)\": \"1349.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"166.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000322\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1201/9781420049718.ch22\", \"Electrical resistivity (\\u03a9cm)\": \"0.00085\", \"Seebeck coefficient (\\u03bcCV/K)\": \"122.0\", \"ZT\": \"0.7\", \"formula\": \"Ag0.15Sb0.15Te1.15Ge0.85\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Skrabek 1995\", \"Structure\": \"ICSD #2084, 300K\", \"marker\": \"{'radius': 2.1072486816, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.531\", \"Average atomic mass (g/mol)\": \"105.62\", \"Scarcity (wt fraction/abundance)\": \"605500000.0\", \"HHI (production)\": \"3762.0\", \"HHI (reserves)\": \"3810.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"479.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.973\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1180.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00176\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.75\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00677\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-296.0\", \"ZT\": \"0.52\", \"formula\": \"In0.05Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 1.5474985707, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.738\", \"Average atomic mass (g/mol)\": \"106.08\", \"Scarcity (wt fraction/abundance)\": \"4312000.0\", \"HHI (production)\": \"7219.0\", \"HHI (reserves)\": \"3308.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"739.646\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.042\", \"Atoms per unit cell\": \"32.1\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"148.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00129\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"87400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.083\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.0034\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-276.0\", \"ZT\": \"0.9\", \"formula\": \"In0.1Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 2.6897519256, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.909\", \"Average atomic mass (g/mol)\": \"106.11\", \"Scarcity (wt fraction/abundance)\": \"4314000.0\", \"HHI (production)\": \"7205.0\", \"HHI (reserves)\": \"3304.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"741.144\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.017\", \"Atoms per unit cell\": \"32.2\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"294.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00224\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"76300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.15\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00213\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-266.0\", \"ZT\": \"1.33\", \"formula\": \"In0.15Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 4.0003270672, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.995\", \"Average atomic mass (g/mol)\": \"106.13\", \"Scarcity (wt fraction/abundance)\": \"4316000.0\", \"HHI (production)\": \"7192.0\", \"HHI (reserves)\": \"3300.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"741.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.953\", \"Atoms per unit cell\": \"32.3\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"470.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00333\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"70900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.23\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00175\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-248.0\", \"ZT\": \"1.41\", \"formula\": \"In0.2Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 4.2282451272, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.08\", \"Average atomic mass (g/mol)\": \"106.16\", \"Scarcity (wt fraction/abundance)\": \"4318000.0\", \"HHI (production)\": \"7180.0\", \"HHI (reserves)\": \"3295.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.742\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.924\", \"Atoms per unit cell\": \"32.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"572.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00352\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"61600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.268\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00134\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-248.0\", \"ZT\": \"1.83\", \"formula\": \"In0.25Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 5.4994004013, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.265\", \"Average atomic mass (g/mol)\": \"106.19\", \"Scarcity (wt fraction/abundance)\": \"4320000.0\", \"HHI (production)\": \"7167.0\", \"HHI (reserves)\": \"3291.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.89\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.858\", \"Atoms per unit cell\": \"32.5\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"746.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00458\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"61500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.321\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00179\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-247.0\", \"ZT\": \"1.36\", \"formula\": \"In0.3Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 4.0924345481, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.159\", \"Average atomic mass (g/mol)\": \"106.21\", \"Scarcity (wt fraction/abundance)\": \"4322000.0\", \"HHI (production)\": \"7154.0\", \"HHI (reserves)\": \"3287.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.89\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.788\", \"Atoms per unit cell\": \"32.6\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"558.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00341\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"61200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.252\"}, {\"doi\": \"10.1557/jmr.2011.163\", \"Electrical resistivity (\\u03a9cm)\": \"0.00129\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-214.0\", \"ZT\": \"1.43\", \"formula\": \"In0.2Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Biswas 2011\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 4.2834911226, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.214\", \"Average atomic mass (g/mol)\": \"106.16\", \"Scarcity (wt fraction/abundance)\": \"4318000.0\", \"HHI (production)\": \"7180.0\", \"HHI (reserves)\": \"3295.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.742\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.924\", \"Atoms per unit cell\": \"32.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"777.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00357\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"46000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.342\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.000569\", \"Seebeck coefficient (\\u03bcCV/K)\": \"105.0\", \"ZT\": \"0.77\", \"formula\": \"Na0.02Pb1Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 2.3234127298, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.675\", \"Average atomic mass (g/mol)\": \"165.97\", \"Scarcity (wt fraction/abundance)\": \"380700000.0\", \"HHI (production)\": \"2781.0\", \"HHI (reserves)\": \"2979.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1760.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.641\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.000619\", \"Seebeck coefficient (\\u03bcCV/K)\": \"98.0\", \"ZT\": \"0.62\", \"formula\": \"Na0.02Pb1Te0.85Se0.15\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 1.8745033128, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.218\", \"Average atomic mass (g/mol)\": \"162.36\", \"Scarcity (wt fraction/abundance)\": \"331500000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2827.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1620.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00156\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9670.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.711\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.000691\", \"Seebeck coefficient (\\u03bcCV/K)\": \"90.0\", \"ZT\": \"0.47\", \"formula\": \"Na0.02Pb1Te0.75Se0.25\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 1.3994083779, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.154\", \"Average atomic mass (g/mol)\": \"159.95\", \"Scarcity (wt fraction/abundance)\": \"297500000.0\", \"HHI (production)\": \"2736.0\", \"HHI (reserves)\": \"2721.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1450.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00117\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8060.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.656\"}, {\"doi\": \"10.1126/science.1159725\", \"Electrical resistivity (\\u03a9cm)\": \"0.00355\", \"Seebeck coefficient (\\u03bcCV/K)\": \"201.0\", \"ZT\": \"0.46\", \"formula\": \"Tl0.01Pb0.99Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Heremans 2008\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 1.3736453037, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.552\", \"Average atomic mass (g/mol)\": \"167.39\", \"Scarcity (wt fraction/abundance)\": \"381200000.0\", \"HHI (production)\": \"2806.0\", \"HHI (reserves)\": \"3012.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"282.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00114\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.177\"}, {\"doi\": \"10.1126/science.1159725\", \"Electrical resistivity (\\u03a9cm)\": \"0.00291\", \"Seebeck coefficient (\\u03bcCV/K)\": \"195.0\", \"ZT\": \"0.52\", \"formula\": \"Tl0.02Pb0.98Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Heremans 2008\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 1.5719602502, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.656\", \"Average atomic mass (g/mol)\": \"167.37\", \"Scarcity (wt fraction/abundance)\": \"381300000.0\", \"HHI (production)\": \"2829.0\", \"HHI (reserves)\": \"3041.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"344.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00131\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.203\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00208\", \"Seebeck coefficient (\\u03bcCV/K)\": \"192.0\", \"ZT\": \"0.71\", \"formula\": \"Si0.9Ge0.1\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"400\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 2.1267692308, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.54\", \"Scarcity (wt fraction/abundance)\": \"153900.0\", \"HHI (production)\": \"4833.0\", \"HHI (reserves)\": \"1200.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"481.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00177\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.0017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"161.0\", \"ZT\": \"0.61\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"400\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.8243519062, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"587.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00152\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.00152\", \"Seebeck coefficient (\\u03bcCV/K)\": \"151.0\", \"ZT\": \"0.6\", \"formula\": \"Si0.79936Ge0.19984B0.0008\", \"comment\": \"\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.8105782086, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"4.145\", \"Average atomic mass (g/mol)\": \"36.98\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4927.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"659.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00151\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.155\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.00134\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-150.0\", \"ZT\": \"0.67\", \"formula\": \"Si0.7956Ge0.1989P0.0055\", \"comment\": \"\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 2.023124859, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"4.229\", \"Average atomic mass (g/mol)\": \"36.96\", \"Scarcity (wt fraction/abundance)\": \"269600.0\", \"HHI (production)\": \"4914.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"749.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00169\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.173\"}, {\"doi\": \"10.1063/1.4765358\", \"Electrical resistivity (\\u03a9cm)\": \"0.0051\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-245.0\", \"ZT\": \"0.47\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"Magnetic levitation induction furnace\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Douglas 2012\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 1.4123529412, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.72\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"196.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00118\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"60000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.028\"}, {\"doi\": \"10.1063/1.1502190\", \"Electrical resistivity (\\u03a9cm)\": \"0.00238\", \"Seebeck coefficient (\\u03bcCV/K)\": \"120.0\", \"ZT\": \"0.24\", \"formula\": \"Bi2Sr2Co2O8\", \"comment\": \"\", \"synthesis\": \"Solid state reaction + extra\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Funahashi 2002\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 0.7254530799, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.125\", \"Average atomic mass (g/mol)\": \"59.93\", \"Scarcity (wt fraction/abundance)\": \"29310000.0\", \"HHI (production)\": \"4016.0\", \"HHI (reserves)\": \"4061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.53\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.59\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"420.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000605\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.193\"}, {\"doi\": \"10.1143/JJAP.39.L1127\", \"Electrical resistivity (\\u03a9cm)\": \"0.00147\", \"Seebeck coefficient (\\u03bcCV/K)\": \"142.0\", \"ZT\": \"0.55\", \"formula\": \"Ca2Co2O5\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Funahashi 2000\", \"Structure\": \"ICSD #55458, 300K\", \"marker\": \"{'radius': 1.6582469264, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.35\", \"Average atomic mass (g/mol)\": \"30.89\", \"Scarcity (wt fraction/abundance)\": \"15420.0\", \"HHI (production)\": \"2551.0\", \"HHI (reserves)\": \"1702.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"236.38\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.883\", \"Atoms per unit cell\": \"21.72\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"682.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00138\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.283\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00119\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-31.0\", \"ZT\": \"0.03\", \"formula\": \"W1O2.9\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24736, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.176\", \"Average atomic mass (g/mol)\": \"59.04\", \"Scarcity (wt fraction/abundance)\": \"679600.0\", \"HHI (production)\": \"5675.0\", \"HHI (reserves)\": \"3532.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1066.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.328\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"840.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.28e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"987.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.258\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"9.79e-05\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-25.0\", \"ZT\": \"0.26\", \"formula\": \"W1O2.722\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24731, 300K\", \"marker\": \"{'radius': 0.7792602976, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"7.817\", \"Average atomic mass (g/mol)\": \"61.09\", \"Scarcity (wt fraction/abundance)\": \"688100.0\", \"HHI (production)\": \"5740.0\", \"HHI (reserves)\": \"3570.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"883.29\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.268\", \"Atoms per unit cell\": \"72.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"10200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000649\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"635.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.276\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"140.0\", \"ZT\": \"0.07\", \"formula\": \"La1.95Sr0.05Cu1O4\", \"comment\": \"Seebeck extrapolated from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78632, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.54\", \"Scarcity (wt fraction/abundance)\": \"20920.0\", \"HHI (production)\": \"6746.0\", \"HHI (reserves)\": \"2457.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.25\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.58\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"92.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000182\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00382\", \"Seebeck coefficient (\\u03bcCV/K)\": \"50.0\", \"ZT\": \"0.03\", \"formula\": \"La1.9Sr0.1Cu1O4\", \"comment\": \"Seebeck estimated Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78240, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.17\", \"Scarcity (wt fraction/abundance)\": \"20610.0\", \"HHI (production)\": \"6670.0\", \"HHI (reserves)\": \"2451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"378.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.514\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"262.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.55e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00149\", \"Seebeck coefficient (\\u03bcCV/K)\": \"20.0\", \"ZT\": \"0.01\", \"formula\": \"La1.85Sr0.15Cu1O4\", \"comment\": \"Seebeck extrapolated from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.81\", \"Scarcity (wt fraction/abundance)\": \"20290.0\", \"HHI (production)\": \"6594.0\", \"HHI (reserves)\": \"2445.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"672.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.69e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.000676\", \"Seebeck coefficient (\\u03bcCV/K)\": \"0.0\", \"ZT\": \"5.92e-07\", \"formula\": \"La1.725Sr0.28Cu1O4\", \"comment\": \"Seebeck estimated Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.92\", \"Scarcity (wt fraction/abundance)\": \"19470.0\", \"HHI (production)\": \"6396.0\", \"HHI (reserves)\": \"2431.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1480.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.48e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"0.01\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"240.0\", \"ZT\": \"0.14\", \"formula\": \"Tl1Cr5Se8\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Nunna 2012\", \"Structure\": \"ICSD #37123, 300K\", \"marker\": \"{'radius': 0.432, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"78.29\", \"Scarcity (wt fraction/abundance)\": \"11800000.0\", \"HHI (production)\": \"3230.0\", \"HHI (reserves)\": \"3274.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"581.29\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.76\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"62.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.00036\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"57600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c2jm16297k\", \"Electrical resistivity (\\u03a9cm)\": \"85.3\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-147.0\", \"ZT\": \"1.01e-05\", \"formula\": \"Li1Mn2O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (oxalates)\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sparks 2012\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.012\", \"Power Factor (W/(K\\u00b2m))\": \"2.53e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.07\", \"Seebeck coefficient (\\u03bcCV/K)\": \"299.0\", \"ZT\": \"0.05\", \"formula\": \"Cu1Fe0.9Cr0.1O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #31918, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.75\", \"Scarcity (wt fraction/abundance)\": \"6756.0\", \"HHI (production)\": \"1683.0\", \"HHI (reserves)\": \"1344.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"136.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.412\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"14.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000128\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"89400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00194\", \"Seebeck coefficient (\\u03bcCV/K)\": \"115.0\", \"ZT\": \"0.27\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.8209619074, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"516.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000684\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.119\", \"Seebeck coefficient (\\u03bcCV/K)\": \"321.0\", \"ZT\": \"0.03\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"8.396\", \"Power Factor (W/(K\\u00b2m))\": \"8.67e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"103000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"810.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"108.0\", \"ZT\": \"5.72e-07\", \"formula\": \"W1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.96\", \"Scarcity (wt fraction/abundance)\": \"674900.0\", \"HHI (production)\": \"5639.0\", \"HHI (reserves)\": \"3511.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00123\", \"Power Factor (W/(K\\u00b2m))\": \"1.43e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"708.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"97.0\", \"ZT\": \"5.32e-07\", \"formula\": \"W0.99O2.97Co0.02O0.03\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.65\", \"Scarcity (wt fraction/abundance)\": \"670200.0\", \"HHI (production)\": \"5615.0\", \"HHI (reserves)\": \"3500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00141\", \"Power Factor (W/(K\\u00b2m))\": \"1.33e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9420.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"99.4\", \"Seebeck coefficient (\\u03bcCV/K)\": \"106.0\", \"ZT\": \"4.52e-06\", \"formula\": \"W0.95O2.95Co0.1O0.15\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.45\", \"Scarcity (wt fraction/abundance)\": \"646800.0\", \"HHI (production)\": \"5484.0\", \"HHI (reserves)\": \"3437.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.01\", \"Power Factor (W/(K\\u00b2m))\": \"1.13e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"176.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"106.0\", \"ZT\": \"2.54e-06\", \"formula\": \"W0.9O2.7Co0.2O0.3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"54.94\", \"Scarcity (wt fraction/abundance)\": \"627100.0\", \"HHI (production)\": \"5394.0\", \"HHI (reserves)\": \"3402.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00569\", \"Power Factor (W/(K\\u00b2m))\": \"6.34e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.242\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-587.0\", \"ZT\": \"0.06\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.067\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.138\", \"Power Factor (W/(K\\u00b2m))\": \"0.000143\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"345000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00132\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-125.0\", \"ZT\": \"0.06\", \"formula\": \"Ca1Yb0.05Mn0.95O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.472\", \"Average atomic mass (g/mol)\": \"29.78\", \"Scarcity (wt fraction/abundance)\": \"19730.0\", \"HHI (production)\": \"2309.0\", \"HHI (reserves)\": \"1374.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"94.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000147\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.063\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00438\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-60.0\", \"ZT\": \"0.03\", \"formula\": \"Ca1Yb0.1Mn0.9O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.639\", \"Average atomic mass (g/mol)\": \"30.96\", \"Scarcity (wt fraction/abundance)\": \"37590.0\", \"HHI (production)\": \"2722.0\", \"HHI (reserves)\": \"1465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"228.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.24e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3610.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.136\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00359\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-49.0\", \"ZT\": \"0.03\", \"formula\": \"Ca1Yb0.15Mn0.85O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.571\", \"Average atomic mass (g/mol)\": \"32.15\", \"Scarcity (wt fraction/abundance)\": \"54140.0\", \"HHI (production)\": \"3105.0\", \"HHI (reserves)\": \"1549.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"279.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.73e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2420.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.173\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-20.0\", \"ZT\": \"0.00133\", \"formula\": \"Ca1Yb0.4Mn0.6O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"121500.0\", \"HHI (production)\": \"4663.0\", \"HHI (reserves)\": \"1891.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"82.8\", \"Power Factor (W/(K\\u00b2m))\": \"3.32e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"401.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-173.0\", \"ZT\": \"0.08\", \"formula\": \"In2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"6.773\", \"Average atomic mass (g/mol)\": \"55.53\", \"Scarcity (wt fraction/abundance)\": \"4035000.0\", \"HHI (production)\": \"2843.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"66.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.0002\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00964\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00235\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-106.0\", \"ZT\": \"0.19\", \"formula\": \"In1.998Ge0.002O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.5719846229, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"6.853\", \"Average atomic mass (g/mol)\": \"55.51\", \"Scarcity (wt fraction/abundance)\": \"4032000.0\", \"HHI (production)\": \"2844.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"426.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000477\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.061\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.000942\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-62.0\", \"ZT\": \"0.17\", \"formula\": \"In1.994Ge0.006O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.4970626911, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"7.207\", \"Average atomic mass (g/mol)\": \"55.48\", \"Scarcity (wt fraction/abundance)\": \"4027000.0\", \"HHI (production)\": \"2846.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1060.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000414\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.144\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.000818\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-57.0\", \"ZT\": \"0.16\", \"formula\": \"In1.985Ge0.015O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.4698995123, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"7.048\", \"Average atomic mass (g/mol)\": \"55.4\", \"Scarcity (wt fraction/abundance)\": \"4016000.0\", \"HHI (production)\": \"2850.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1220.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000392\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.169\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.000995\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-61.0\", \"ZT\": \"0.15\", \"formula\": \"In1.94Ge0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.4429728301, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"6.604\", \"Average atomic mass (g/mol)\": \"55.02\", \"Scarcity (wt fraction/abundance)\": \"3961000.0\", \"HHI (production)\": \"2869.0\", \"HHI (reserves)\": \"1737.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000369\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3670.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.148\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00143\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-66.0\", \"ZT\": \"0.12\", \"formula\": \"In1.9Ge0.1O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.3596533132, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"5.091\", \"Average atomic mass (g/mol)\": \"54.68\", \"Scarcity (wt fraction/abundance)\": \"3910000.0\", \"HHI (production)\": \"2887.0\", \"HHI (reserves)\": \"1734.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"697.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0003\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.134\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.0028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-64.0\", \"ZT\": \"0.06\", \"formula\": \"In1.8Ge0.2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.611\", \"Average atomic mass (g/mol)\": \"53.84\", \"Scarcity (wt fraction/abundance)\": \"3782000.0\", \"HHI (production)\": \"2932.0\", \"HHI (reserves)\": \"1727.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"358.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000147\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.134\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.384\", \"Seebeck coefficient (\\u03bcCV/K)\": \"140.0\", \"ZT\": \"0.00205\", \"formula\": \"La1Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.17\", \"Scarcity (wt fraction/abundance)\": \"24200.0\", \"HHI (production)\": \"6184.0\", \"HHI (reserves)\": \"2502.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.605\", \"Power Factor (W/(K\\u00b2m))\": \"5.13e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.074\", \"Seebeck coefficient (\\u03bcCV/K)\": \"304.0\", \"ZT\": \"0.05\", \"formula\": \"La0.99Sr0.01Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.06\", \"Scarcity (wt fraction/abundance)\": \"24100.0\", \"HHI (production)\": \"6158.0\", \"HHI (reserves)\": \"2500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"13.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000125\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"92400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.034\", \"Seebeck coefficient (\\u03bcCV/K)\": \"244.0\", \"ZT\": \"0.07\", \"formula\": \"La0.98Sr0.02Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.96\", \"Scarcity (wt fraction/abundance)\": \"24010.0\", \"HHI (production)\": \"6132.0\", \"HHI (reserves)\": \"2499.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"29.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000175\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"59300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00728\", \"Seebeck coefficient (\\u03bcCV/K)\": \"129.0\", \"ZT\": \"0.09\", \"formula\": \"La0.95Sr0.05Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247230, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.65\", \"Scarcity (wt fraction/abundance)\": \"23720.0\", \"HHI (production)\": \"6053.0\", \"HHI (reserves)\": \"2493.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.147\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"137.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000229\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000447\", \"Seebeck coefficient (\\u03bcCV/K)\": \"18.0\", \"ZT\": \"0.03\", \"formula\": \"La0.8Sr0.2Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247232, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.12\", \"Scarcity (wt fraction/abundance)\": \"22220.0\", \"HHI (production)\": \"5646.0\", \"HHI (reserves)\": \"2465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"224.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.21\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2240.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.93e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"310.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1021/cm060261t\", \"Electrical resistivity (\\u03a9cm)\": \"0.00232\", \"Seebeck coefficient (\\u03bcCV/K)\": \"69.0\", \"ZT\": \"0.08\", \"formula\": \"Yb14Mn1Sb11\", \"comment\": \"\", \"synthesis\": \"flux (Sn), Ar\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Brown 2006\", \"Structure\": \"ICSD #85638, 143K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.844\", \"Average atomic mass (g/mol)\": \"146.81\", \"Scarcity (wt fraction/abundance)\": \"1966000.0\", \"HHI (production)\": \"8812.0\", \"HHI (reserves)\": \"3211.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"6058.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.129\", \"Atoms per unit cell\": \"208.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"430.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000203\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4720.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.498\"}, {\"doi\": \"10.1016/S0022-3697(96)00228-4\", \"Electrical resistivity (\\u03a9cm)\": \"0.00259\", \"Seebeck coefficient (\\u03bcCV/K)\": \"146.0\", \"ZT\": \"0.33\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"melted, inert\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Caillat 1997\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 0.9879350915, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.664\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"386.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000823\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.568\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.00385\", \"Seebeck coefficient (\\u03bcCV/K)\": \"154.0\", \"ZT\": \"0.25\", \"formula\": \"Ce1Fe2Co2Sb12\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.7392, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.69\", \"Scarcity (wt fraction/abundance)\": \"3994000.0\", \"HHI (production)\": \"7379.0\", \"HHI (reserves)\": \"3223.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"260.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000616\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.00112\", \"Seebeck coefficient (\\u03bcCV/K)\": \"127.0\", \"ZT\": \"0.58\", \"formula\": \"Ce1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 1.7281071429, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.98\", \"Average atomic mass (g/mol)\": \"107.51\", \"Scarcity (wt fraction/abundance)\": \"4000000.0\", \"HHI (production)\": \"7367.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"893.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00144\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.44\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.000971\", \"Seebeck coefficient (\\u03bcCV/K)\": \"107.0\", \"ZT\": \"0.47\", \"formula\": \"Ce1Fe3.5Co0.5Sb13\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 1.4149124614, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.38\", \"Average atomic mass (g/mol)\": \"108.22\", \"Scarcity (wt fraction/abundance)\": \"4065000.0\", \"HHI (production)\": \"7395.0\", \"HHI (reserves)\": \"3181.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1030.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00118\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.422\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.000836\", \"Seebeck coefficient (\\u03bcCV/K)\": \"76.0\", \"ZT\": \"0.27\", \"formula\": \"Ce1Fe4Sb12\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.8225583732, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.57\", \"Average atomic mass (g/mol)\": \"107.33\", \"Scarcity (wt fraction/abundance)\": \"4005000.0\", \"HHI (production)\": \"7355.0\", \"HHI (reserves)\": \"3146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"762.5\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.426\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000685\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5730.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.744\"}, {\"doi\": \"10.1021/cm200581k\", \"Electrical resistivity (\\u03a9cm)\": \"0.04\", \"Seebeck coefficient (\\u03bcCV/K)\": \"300.0\", \"ZT\": \"0.09\", \"formula\": \"Ag1Cr1Se2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, sealed\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Gascoin 2011\", \"Structure\": \"ICSD #68423, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.4\", \"Average atomic mass (g/mol)\": \"79.45\", \"Scarcity (wt fraction/abundance)\": \"14290000.0\", \"HHI (production)\": \"2031.0\", \"HHI (reserves)\": \"2077.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"248.9\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.742\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.000224\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"90100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.061\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.05\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-135.0\", \"ZT\": \"0.01\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"19.8\", \"Power Factor (W/(K\\u00b2m))\": \"3.61e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-128.0\", \"ZT\": \"0.04\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"66.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.00011\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-123.0\", \"ZT\": \"0.06\", \"formula\": \"Zn0.9925Al0.0075O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"10740.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1618.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"97.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000148\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00709\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-117.0\", \"ZT\": \"0.08\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"141.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.021\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-150.0\", \"ZT\": \"0.04\", \"formula\": \"Zn0.97Al0.03O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.11\", \"Scarcity (wt fraction/abundance)\": \"10610.0\", \"HHI (production)\": \"1360.0\", \"HHI (reserves)\": \"1608.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000105\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-74.0\", \"ZT\": \"0.00837\", \"formula\": \"Sr1Mn0.98Mo0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.28\", \"Scarcity (wt fraction/abundance)\": \"10260.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"38.4\", \"Power Factor (W/(K\\u00b2m))\": \"2.09e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5450.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-105.0\", \"ZT\": \"0.03\", \"formula\": \"Sr1Mn0.96Mo0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.44\", \"Scarcity (wt fraction/abundance)\": \"18890.0\", \"HHI (production)\": \"2515.0\", \"HHI (reserves)\": \"2089.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"65.9\", \"Power Factor (W/(K\\u00b2m))\": \"7.27e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.02.061\", \"Electrical resistivity (\\u03a9cm)\": \"0.00117\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-136.0\", \"ZT\": \"0.63\", \"formula\": \"Zr1Ni1.98Cu0.02Sn1\", \"comment\": \"\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Katsumyama 2004\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 1.8986484175, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.795\", \"Average atomic mass (g/mol)\": \"81.85\", \"Scarcity (wt fraction/abundance)\": \"165700.0\", \"HHI (production)\": \"2246.0\", \"HHI (reserves)\": \"1848.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"855.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00158\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.123\"}, {\"doi\": \"10.1016/j.jallcom.2004.02.061\", \"Electrical resistivity (\\u03a9cm)\": \"0.00695\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-130.0\", \"ZT\": \"0.1\", \"formula\": \"Zr1Ni0.76Co0.004Cu0.2Sn1\", \"comment\": \"\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Katsumyama 2004\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.3\", \"Average atomic mass (g/mol)\": \"90.24\", \"Scarcity (wt fraction/abundance)\": \"201300.0\", \"HHI (production)\": \"2555.0\", \"HHI (reserves)\": \"1934.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"144.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000243\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.026\"}, {\"doi\": \"10.1016/j.jallcom.2006.02.075\", \"Electrical resistivity (\\u03a9cm)\": \"0.000624\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-137.0\", \"ZT\": \"1.2\", \"formula\": \"Zr1Ni1Sn0.98Sb0.02\", \"comment\": \"\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Katsumyama 2007\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 3.6094230769, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.95\", \"Average atomic mass (g/mol)\": \"89.56\", \"Scarcity (wt fraction/abundance)\": \"241400.0\", \"HHI (production)\": \"2567.0\", \"HHI (reserves)\": \"1945.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1600.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00301\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.197\"}, {\"doi\": \"10.1016/j.jallcom.2006.02.075\", \"Electrical resistivity (\\u03a9cm)\": \"0.000788\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-109.0\", \"ZT\": \"0.6\", \"formula\": \"Zr0.94Y0.06Ni1Sn0.96Sb0.04\", \"comment\": \"\", \"synthesis\": \"arc melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Katsumyama 2007\", \"Structure\": \"ICSD #105382, 300K\", \"marker\": \"{'radius': 1.8092893401, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.51\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"283400.0\", \"HHI (production)\": \"2742.0\", \"HHI (reserves)\": \"1962.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"228.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"19.037\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1270.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00151\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.19\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00141\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-137.0\", \"ZT\": \"0.53\", \"formula\": \"Nb1Co1Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 1.5919122522, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.958\", \"Average atomic mass (g/mol)\": \"90.18\", \"Scarcity (wt fraction/abundance)\": \"221500.0\", \"HHI (production)\": \"4729.0\", \"HHI (reserves)\": \"4317.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"707.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00133\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.087\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00163\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-185.0\", \"ZT\": \"0.84\", \"formula\": \"Nb1Co1.05Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 2.5294920227, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.01\", \"Average atomic mass (g/mol)\": \"89.67\", \"Scarcity (wt fraction/abundance)\": \"219500.0\", \"HHI (production)\": \"4711.0\", \"HHI (reserves)\": \"4299.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"613.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00211\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.085\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.0013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-152.0\", \"ZT\": \"0.71\", \"formula\": \"Nb1Co1.10Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 2.1357993184, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.83\", \"Average atomic mass (g/mol)\": \"89.17\", \"Scarcity (wt fraction/abundance)\": \"217500.0\", \"HHI (production)\": \"4693.0\", \"HHI (reserves)\": \"4281.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"771.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00178\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.129\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000155\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-69.0\", \"ZT\": \"1.24\", \"formula\": \"Bi92Sb8\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"400\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 3.7076266875, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"202.0\", \"Scarcity (wt fraction/abundance)\": \"56230000.0\", \"HHI (production)\": \"5422.0\", \"HHI (reserves)\": \"5869.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"6430.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00309\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000181\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-69.0\", \"ZT\": \"1.04\", \"formula\": \"Bi90Sb10\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"400\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 3.1158521285, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"200.26\", \"Scarcity (wt fraction/abundance)\": \"55550000.0\", \"HHI (production)\": \"5455.0\", \"HHI (reserves)\": \"5836.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5530.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0026\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4690.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000168\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-73.0\", \"ZT\": \"1.26\", \"formula\": \"Bi88Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"400\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 3.7935823821, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"198.51\", \"Scarcity (wt fraction/abundance)\": \"54860000.0\", \"HHI (production)\": \"5488.0\", \"HHI (reserves)\": \"5804.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5960.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00316\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5310.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000293\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-69.0\", \"ZT\": \"0.65\", \"formula\": \"Bi86Sb14\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"400\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 1.9582697436, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"196.77\", \"Scarcity (wt fraction/abundance)\": \"54160000.0\", \"HHI (production)\": \"5522.0\", \"HHI (reserves)\": \"5770.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3420.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00163\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4780.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jpcs.2004.01.010\", \"Electrical resistivity (\\u03a9cm)\": \"0.000285\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-62.0\", \"ZT\": \"0.53\", \"formula\": \"Bi83Sb17\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polcrystalline\", \"temperature\": \"400\", \"author\": \"Kitagawa 2004\", \"Structure\": \"ICSD #617054, 300K\", \"marker\": \"{'radius': 1.5964561447, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"194.15\", \"Scarcity (wt fraction/abundance)\": \"53090000.0\", \"HHI (production)\": \"5574.0\", \"HHI (reserves)\": \"5719.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"195.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.598\", \"Atoms per unit cell\": \"6.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3510.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00133\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3790.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.173\", \"Seebeck coefficient (\\u03bcCV/K)\": \"9.0\", \"ZT\": \"2e-05\", \"formula\": \"Ca1Mn6.5Cu0.5O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.05\", \"Scarcity (wt fraction/abundance)\": \"1387.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1359.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5.793\", \"Power Factor (W/(K\\u00b2m))\": \"5e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"86.3\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.101\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-20.0\", \"ZT\": \"0.000157\", \"formula\": \"Ca1Mn6Cu1O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.26\", \"Scarcity (wt fraction/abundance)\": \"2126.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1348.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.895\", \"Power Factor (W/(K\\u00b2m))\": \"3.93e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"397.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"74.1\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-46.0\", \"ZT\": \"1.14e-06\", \"formula\": \"Li1Mn2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.013\", \"Power Factor (W/(K\\u00b2m))\": \"2.85e-09\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2120.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.03\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-23.0\", \"ZT\": \"0.000696\", \"formula\": \"Pr0.5Ca0.5Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #85650, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.69\", \"Scarcity (wt fraction/abundance)\": \"40990.0\", \"HHI (production)\": \"4428.0\", \"HHI (reserves)\": \"1928.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"221.92\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.096\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"33.5\", \"Power Factor (W/(K\\u00b2m))\": \"1.74e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"518.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00072\", \"Seebeck coefficient (\\u03bcCV/K)\": \"8.0\", \"ZT\": \"0.00313\", \"formula\": \"Mo3Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.912\", \"Average atomic mass (g/mol)\": \"114.04\", \"Scarcity (wt fraction/abundance)\": \"639700000.0\", \"HHI (production)\": \"2718.0\", \"HHI (reserves)\": \"5052.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1390.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.83e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"56.4\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.347\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000783\", \"Seebeck coefficient (\\u03bcCV/K)\": \"5.0\", \"ZT\": \"0.00153\", \"formula\": \"Mo6Te7S1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.097\", \"Average atomic mass (g/mol)\": \"107.22\", \"Scarcity (wt fraction/abundance)\": \"595400000.0\", \"HHI (production)\": \"2661.0\", \"HHI (reserves)\": \"4975.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1280.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.84e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.402\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000887\", \"Seebeck coefficient (\\u03bcCV/K)\": \"8.0\", \"ZT\": \"0.00293\", \"formula\": \"Mo6Te6S2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.374\", \"Average atomic mass (g/mol)\": \"100.39\", \"Scarcity (wt fraction/abundance)\": \"545100000.0\", \"HHI (production)\": \"2596.0\", \"HHI (reserves)\": \"4888.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1130.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.33e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"65.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.463\"}, {\"doi\": \"10.1109/ICT.2006.331289\", \"Electrical resistivity (\\u03a9cm)\": \"0.0027\", \"Seebeck coefficient (\\u03bcCV/K)\": \"153.0\", \"ZT\": \"0.35\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kuriyama 2006\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 1.0401561883, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"9.767\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"370.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000867\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.037\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00567\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-68.0\", \"ZT\": \"0.03\", \"formula\": \"Sr2Ti0.8Nb0.2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.59\", \"Average atomic mass (g/mol)\": \"42.3\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3261.0\", \"HHI (reserves)\": \"2636.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"187.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.357\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"176.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.06e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4570.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.048\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-57.0\", \"ZT\": \"0.06\", \"formula\": \"Sr3Ti1.6Nb0.4O7\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.89\", \"Average atomic mass (g/mol)\": \"40.72\", \"Scarcity (wt fraction/abundance)\": \"5611.0\", \"HHI (production)\": \"3187.0\", \"HHI (reserves)\": \"2641.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"305.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.708\", \"Atoms per unit cell\": \"24.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"460.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00015\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3270.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.115\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00142\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-62.0\", \"ZT\": \"0.11\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162889, 15K\", \"marker\": \"{'radius': 0.3289448448, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"8.62\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"240.63\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.032\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"704.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000274\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3890.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.08\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00443\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-188.0\", \"ZT\": \"0.32\", \"formula\": \"Sr0.95La0.05Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 0.957969431, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.21\", \"Scarcity (wt fraction/abundance)\": \"2291.0\", \"HHI (production)\": \"2640.0\", \"HHI (reserves)\": \"1987.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"226.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000798\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00165\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-115.0\", \"ZT\": \"0.32\", \"formula\": \"Sr0.9La0.1Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 0.961629954, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"5.28\", \"Average atomic mass (g/mol)\": \"37.72\", \"Scarcity (wt fraction/abundance)\": \"3205.0\", \"HHI (production)\": \"2856.0\", \"HHI (reserves)\": \"2006.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"606.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000801\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.112\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.000534\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-65.0\", \"ZT\": \"0.31\", \"formula\": \"Sr0.8La0.2Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65094, 300K\", \"marker\": \"{'radius': 0.9412624297, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.75\", \"Scarcity (wt fraction/abundance)\": \"4961.0\", \"HHI (production)\": \"3271.0\", \"HHI (reserves)\": \"2041.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.0\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1870.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000784\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4190.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00839\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-296.0\", \"ZT\": \"0.42\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 1.2517901042, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.195\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"119.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00104\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"87600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.022\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00124\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-192.0\", \"ZT\": \"1.19\", \"formula\": \"Ti0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 3.5842368496, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.862\", \"Average atomic mass (g/mol)\": \"75.24\", \"Scarcity (wt fraction/abundance)\": \"236100.0\", \"HHI (production)\": \"1890.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"806.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00299\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"37000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.134\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000727\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-159.0\", \"ZT\": \"1.38\", \"formula\": \"Ti0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 4.1494269807, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.328\", \"Average atomic mass (g/mol)\": \"75.39\", \"Scarcity (wt fraction/abundance)\": \"235900.0\", \"HHI (production)\": \"1918.0\", \"HHI (reserves)\": \"1638.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1380.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00346\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.212\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000396\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-111.0\", \"ZT\": \"1.24\", \"formula\": \"Ti0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 3.731724129, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.378\", \"Average atomic mass (g/mol)\": \"75.84\", \"Scarcity (wt fraction/abundance)\": \"235200.0\", \"HHI (production)\": \"2004.0\", \"HHI (reserves)\": \"1726.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2530.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00311\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.387\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00874\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-343.0\", \"ZT\": \"0.54\", \"formula\": \"Zr1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.6118759454, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"8.395\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"200100.0\", \"HHI (production)\": \"2519.0\", \"HHI (reserves)\": \"1929.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"114.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00134\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"117000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.013\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00124\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-189.0\", \"ZT\": \"1.15\", \"formula\": \"Zr0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 3.4568181943, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"8.212\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200200.0\", \"HHI (production)\": \"2537.0\", \"HHI (reserves)\": \"1950.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"806.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00288\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.096\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000691\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-148.0\", \"ZT\": \"1.27\", \"formula\": \"Zr0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 3.8143139543, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"8.678\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200400.0\", \"HHI (production)\": \"2554.0\", \"HHI (reserves)\": \"1972.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1450.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00318\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.163\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000364\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.87\", \"formula\": \"Zr0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 2.610589691, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"8.212\", \"Average atomic mass (g/mol)\": \"89.57\", \"Scarcity (wt fraction/abundance)\": \"200900.0\", \"HHI (production)\": \"2608.0\", \"HHI (reserves)\": \"2036.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2740.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00218\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7930.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.326\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"58.0\", \"ZT\": \"0.00328\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.4\", \"Power Factor (W/(K\\u00b2m))\": \"8.2e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3360.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.038\", \"Seebeck coefficient (\\u03bcCV/K)\": \"70.0\", \"ZT\": \"0.00518\", \"formula\": \"La0.05Ca2.85Co3.8O8.55\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.6\", \"Scarcity (wt fraction/abundance)\": \"17300.0\", \"HHI (production)\": \"2612.0\", \"HHI (reserves)\": \"1776.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"26.4\", \"Power Factor (W/(K\\u00b2m))\": \"1.3e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.039\", \"Seebeck coefficient (\\u03bcCV/K)\": \"68.0\", \"ZT\": \"0.00485\", \"formula\": \"La0.3Ca2.7Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"33.1\", \"Scarcity (wt fraction/abundance)\": \"18350.0\", \"HHI (production)\": \"3029.0\", \"HHI (reserves)\": \"1870.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"25.9\", \"Power Factor (W/(K\\u00b2m))\": \"1.21e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4690.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.037\", \"Seebeck coefficient (\\u03bcCV/K)\": \"73.0\", \"ZT\": \"0.00574\", \"formula\": \"La0.45Ca2.55Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"34.03\", \"Scarcity (wt fraction/abundance)\": \"18900.0\", \"HHI (production)\": \"3266.0\", \"HHI (reserves)\": \"1923.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"26.8\", \"Power Factor (W/(K\\u00b2m))\": \"1.43e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5340.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000552\", \"Seebeck coefficient (\\u03bcCV/K)\": \"27.0\", \"ZT\": \"0.05\", \"formula\": \"Cr1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #40697, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.106\", \"Average atomic mass (g/mol)\": \"58.82\", \"Scarcity (wt fraction/abundance)\": \"557400.0\", \"HHI (production)\": \"1985.0\", \"HHI (reserves)\": \"3955.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.41\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.608\", \"Atoms per unit cell\": \"15.3\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1810.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000133\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"733.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.84\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000737\", \"Seebeck coefficient (\\u03bcCV/K)\": \"31.0\", \"ZT\": \"0.05\", \"formula\": \"Mn1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #249898, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.627\", \"Average atomic mass (g/mol)\": \"59.07\", \"Scarcity (wt fraction/abundance)\": \"554800.0\", \"HHI (production)\": \"1871.0\", \"HHI (reserves)\": \"3777.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"816.76\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.15\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1360.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00013\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"960.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.814\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000673\", \"Seebeck coefficient (\\u03bcCV/K)\": \"28.0\", \"ZT\": \"0.05\", \"formula\": \"Fe1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #632653, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.852\", \"Average atomic mass (g/mol)\": \"59.14\", \"Scarcity (wt fraction/abundance)\": \"554000.0\", \"HHI (production)\": \"1937.0\", \"HHI (reserves)\": \"3740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"807.22\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.938\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1490.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000118\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"795.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.783\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000512\", \"Seebeck coefficient (\\u03bcCV/K)\": \"9.0\", \"ZT\": \"0.00657\", \"formula\": \"Ni2.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602930, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.33\", \"Average atomic mass (g/mol)\": \"59.35\", \"Scarcity (wt fraction/abundance)\": \"528800.0\", \"HHI (production)\": \"1782.0\", \"HHI (reserves)\": \"3642.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"801.34\", \"Average atomic volume (\\u212b\\u00b3)\": \"16.695\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1950.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.64e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"84.1\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.819\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.00102\", \"Seebeck coefficient (\\u03bcCV/K)\": \"62.0\", \"ZT\": \"0.15\", \"formula\": \"Cu4.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602374, 300K\", \"marker\": \"{'radius': 0.4437927158, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.431\", \"Average atomic mass (g/mol)\": \"60.36\", \"Scarcity (wt fraction/abundance)\": \"465000.0\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"3380.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"853.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.807\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"976.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00037\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3790.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.666\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.004\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.1\", \"formula\": \"Ca0.9Bi0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #98592, 300K\", \"marker\": \"{'radius': 0.3049941677, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.147\", \"Average atomic mass (g/mol)\": \"31.98\", \"Scarcity (wt fraction/abundance)\": \"7688000.0\", \"HHI (production)\": \"2260.0\", \"HHI (reserves)\": \"1887.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.57\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.678\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"250.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000254\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.078\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00645\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-55.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.9Ce0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.6\", \"Scarcity (wt fraction/abundance)\": \"1819.0\", \"HHI (production)\": \"2506.0\", \"HHI (reserves)\": \"1440.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"155.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.76e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3070.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-91.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"66.1\", \"Power Factor (W/(K\\u00b2m))\": \"5.5e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8320.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00747\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-106.0\", \"ZT\": \"0.06\", \"formula\": \"Ca0.9Sm0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.81\", \"Scarcity (wt fraction/abundance)\": \"15330.0\", \"HHI (production)\": \"2553.0\", \"HHI (reserves)\": \"1451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"134.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00015\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.115\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-71.0\", \"ZT\": \"0.00175\", \"formula\": \"Ca0.9Sb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.24\", \"Scarcity (wt fraction/abundance)\": \"403100.0\", \"HHI (production)\": \"2295.0\", \"HHI (reserves)\": \"1442.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"8.674\", \"Power Factor (W/(K\\u00b2m))\": \"4.36e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5030.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00699\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-98.0\", \"ZT\": \"0.06\", \"formula\": \"Ca0.9La0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.58\", \"Scarcity (wt fraction/abundance)\": \"2861.0\", \"HHI (production)\": \"2501.0\", \"HHI (reserves)\": \"1438.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"143.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000139\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9680.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.052\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-266.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.9Pb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.95\", \"Scarcity (wt fraction/abundance)\": \"11170.0\", \"HHI (production)\": \"1922.0\", \"HHI (reserves)\": \"1336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"19.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000135\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"70800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.205\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-357.0\", \"ZT\": \"0.02\", \"formula\": \"Ca0.9In0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.1\", \"Scarcity (wt fraction/abundance)\": \"372600.0\", \"HHI (production)\": \"1921.0\", \"HHI (reserves)\": \"1325.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.887\", \"Power Factor (W/(K\\u00b2m))\": \"6.21e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"127000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"2.302\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-282.0\", \"ZT\": \"0.00138\", \"formula\": \"Ca0.9Sn0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"35350.0\", \"HHI (production)\": \"1866.0\", \"HHI (reserves)\": \"1298.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.434\", \"Power Factor (W/(K\\u00b2m))\": \"3.45e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"79400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"2.87\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-461.0\", \"ZT\": \"0.00296\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.178\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.348\", \"Power Factor (W/(K\\u00b2m))\": \"7.41e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"213000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000107\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"18.7\", \"Seebeck coefficient (\\u03bcCV/K)\": \"916.0\", \"ZT\": \"0.0018\", \"formula\": \"Cu1Cr1O2\", \"comment\": \"*res data at 300K/400K extrapolated from 600K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157800, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.156\", \"Average atomic mass (g/mol)\": \"36.88\", \"Scarcity (wt fraction/abundance)\": \"8516.0\", \"HHI (production)\": \"1881.0\", \"HHI (reserves)\": \"2193.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.054\", \"Power Factor (W/(K\\u00b2m))\": \"4.49e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"840000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"8.49e-06\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"1.758\", \"Seebeck coefficient (\\u03bcCV/K)\": \"445.0\", \"ZT\": \"0.0045\", \"formula\": \"Cu1Cr0.99Mg0.01O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157801, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.403\", \"Average atomic mass (g/mol)\": \"36.82\", \"Scarcity (wt fraction/abundance)\": \"8514.0\", \"HHI (production)\": \"1882.0\", \"HHI (reserves)\": \"2184.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.569\", \"Power Factor (W/(K\\u00b2m))\": \"1.13e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"198000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"8.67e-05\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.569\", \"Seebeck coefficient (\\u03bcCV/K)\": \"332.0\", \"ZT\": \"0.00775\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.709\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1.757\", \"Power Factor (W/(K\\u00b2m))\": \"1.94e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"110000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000256\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.069\", \"Seebeck coefficient (\\u03bcCV/K)\": \"241.0\", \"ZT\": \"0.03\", \"formula\": \"Cu1Cr0.97Mg0.03O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157803, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.461\", \"Average atomic mass (g/mol)\": \"36.68\", \"Scarcity (wt fraction/abundance)\": \"8511.0\", \"HHI (production)\": \"1885.0\", \"HHI (reserves)\": \"2165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.928\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"14.4\", \"Power Factor (W/(K\\u00b2m))\": \"8.4e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"58200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00218\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.066\", \"Seebeck coefficient (\\u03bcCV/K)\": \"225.0\", \"ZT\": \"0.03\", \"formula\": \"Cu1Cr0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157804, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"8.767\", \"Average atomic mass (g/mol)\": \"36.61\", \"Scarcity (wt fraction/abundance)\": \"8509.0\", \"HHI (production)\": \"1886.0\", \"HHI (reserves)\": \"2156.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.933\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"15.1\", \"Power Factor (W/(K\\u00b2m))\": \"7.68e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"50800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00168\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.055\", \"Seebeck coefficient (\\u03bcCV/K)\": \"241.0\", \"ZT\": \"0.04\", \"formula\": \"Cu1Cr0.95Mg0.05O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157805, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"9.016\", \"Average atomic mass (g/mol)\": \"36.54\", \"Scarcity (wt fraction/abundance)\": \"8507.0\", \"HHI (production)\": \"1887.0\", \"HHI (reserves)\": \"2146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.16\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.93\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"18.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000107\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"58200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00198\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.000354\", \"Seebeck coefficient (\\u03bcCV/K)\": \"98.0\", \"ZT\": \"1.09\", \"formula\": \"Na1Co2O4\", \"comment\": \"\", \"synthesis\": \"flux (NaCl), air\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 3.2565131393, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"13.53\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2830.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00271\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.204\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.00253\", \"Seebeck coefficient (\\u03bcCV/K)\": \"118.0\", \"ZT\": \"0.22\", \"formula\": \"Na1Co2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 0.660688019, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.834\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"395.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000551\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.21\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00626\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-209.0\", \"ZT\": \"0.28\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 0.8344413398, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.53\", \"Average atomic mass (g/mol)\": \"104.09\", \"Scarcity (wt fraction/abundance)\": \"262000.0\", \"HHI (production)\": \"2643.0\", \"HHI (reserves)\": \"2022.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"160.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000695\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"43500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.044\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00511\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-234.0\", \"ZT\": \"0.43\", \"formula\": \"Zr0.4Hf0.4Ti0.2Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 1.2802022681, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.345\", \"Average atomic mass (g/mol)\": \"98.29\", \"Scarcity (wt fraction/abundance)\": \"258100.0\", \"HHI (production)\": \"2524.0\", \"HHI (reserves)\": \"1954.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"196.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00107\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"54600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.057\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00555\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-379.0\", \"ZT\": \"1.04\", \"formula\": \"Zr0.35Hf0.35Ti0.3Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 3.1113299638, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.837\", \"Average atomic mass (g/mol)\": \"95.39\", \"Scarcity (wt fraction/abundance)\": \"256000.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"180.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00259\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"144000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.062\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00338\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-330.0\", \"ZT\": \"1.29\", \"formula\": \"Zr0.25Hf0.25Ti0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 3.8633799172, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.003\", \"Average atomic mass (g/mol)\": \"89.59\", \"Scarcity (wt fraction/abundance)\": \"251300.0\", \"HHI (production)\": \"2315.0\", \"HHI (reserves)\": \"1836.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"296.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00322\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"109000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.096\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00313\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-265.0\", \"ZT\": \"0.9\", \"formula\": \"Zr0.15Hf0.15Ti0.7Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 2.6858142532, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.072\", \"Average atomic mass (g/mol)\": \"83.79\", \"Scarcity (wt fraction/abundance)\": \"246000.0\", \"HHI (production)\": \"2152.0\", \"HHI (reserves)\": \"1744.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"319.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00224\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"70100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.101\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00106\", \"Seebeck coefficient (\\u03bcCV/K)\": \"87.0\", \"ZT\": \"0.29\", \"formula\": \"Ce1Fe4Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #621065, 300K\", \"marker\": \"{'radius': 0.86021226, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.33\", \"Scarcity (wt fraction/abundance)\": \"4005000.0\", \"HHI (production)\": \"7355.0\", \"HHI (reserves)\": \"3146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"762.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.421\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"947.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000717\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7570.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00163\", \"Seebeck coefficient (\\u03bcCV/K)\": \"108.0\", \"ZT\": \"0.29\", \"formula\": \"Ce1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.8559731988, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.51\", \"Scarcity (wt fraction/abundance)\": \"4000000.0\", \"HHI (production)\": \"7367.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"615.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000713\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00288\", \"Seebeck coefficient (\\u03bcCV/K)\": \"123.0\", \"ZT\": \"0.21\", \"formula\": \"Ce1Fe2.5Co1.5Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.6316404206, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.6\", \"Scarcity (wt fraction/abundance)\": \"3997000.0\", \"HHI (production)\": \"7373.0\", \"HHI (reserves)\": \"3204.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"347.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000526\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00481\", \"Seebeck coefficient (\\u03bcCV/K)\": \"135.0\", \"ZT\": \"0.15\", \"formula\": \"Ce1Fe2Co2Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.4517180311, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.69\", \"Scarcity (wt fraction/abundance)\": \"3994000.0\", \"HHI (production)\": \"7379.0\", \"HHI (reserves)\": \"3223.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"208.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000376\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00985\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-102.0\", \"ZT\": \"0.04\", \"formula\": \"Ce1Fe1Co3Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.88\", \"Scarcity (wt fraction/abundance)\": \"3988000.0\", \"HHI (production)\": \"7391.0\", \"HHI (reserves)\": \"3261.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"101.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000106\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.045\", \"Seebeck coefficient (\\u03bcCV/K)\": \"12.0\", \"ZT\": \"0.000129\", \"formula\": \"Ce1Fe1.5Co2.5Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.78\", \"Scarcity (wt fraction/abundance)\": \"3991000.0\", \"HHI (production)\": \"7385.0\", \"HHI (reserves)\": \"3242.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"22.4\", \"Power Factor (W/(K\\u00b2m))\": \"3.23e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"144.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00183\", \"Seebeck coefficient (\\u03bcCV/K)\": \"143.0\", \"ZT\": \"0.44\", \"formula\": \"La1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #280118, 295K\", \"marker\": \"{'radius': 1.3343273128, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.6\", \"Average atomic mass (g/mol)\": \"107.44\", \"Scarcity (wt fraction/abundance)\": \"4003000.0\", \"HHI (production)\": \"7366.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"752.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.143\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"546.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00111\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.333\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-281.0\", \"ZT\": \"1.46\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1.998Sb0.002\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 4.3705350554, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.713\", \"Average atomic mass (g/mol)\": \"107.74\", \"Scarcity (wt fraction/abundance)\": \"314900.0\", \"HHI (production)\": \"2632.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"461.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00364\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"79000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.166\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00125\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-237.0\", \"ZT\": \"1.79\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1.994Sb0.006\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 5.3810314546, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.646\", \"Average atomic mass (g/mol)\": \"107.75\", \"Scarcity (wt fraction/abundance)\": \"320000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"1919.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"798.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00448\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"56200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.295\"}, {\"doi\": \"http://orbit.dtu.dk/en/publications/improvement-of-niobium-doped-srtio3-by-nanostructuring(2b6f4b33-1a6f-4472-ac18-6996f91cd743).html\", \"Electrical resistivity (\\u03a9cm)\": \"0.00454\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-77.0\", \"ZT\": \"0.05\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Sonne 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"8.57\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"220.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00013\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5930.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.025\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.004\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-70.0\", \"ZT\": \"0.05\", \"formula\": \"Sr1Dy0.08Ti0.92O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.74\", \"Average atomic mass (g/mol)\": \"38.53\", \"Scarcity (wt fraction/abundance)\": \"13120.0\", \"HHI (production)\": \"2920.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"250.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000124\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4970.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.065\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00193\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-42.0\", \"ZT\": \"0.04\", \"formula\": \"Sr1Nd0.17Ti0.83O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.35\", \"Average atomic mass (g/mol)\": \"39.97\", \"Scarcity (wt fraction/abundance)\": \"4528.0\", \"HHI (production)\": \"3337.0\", \"HHI (reserves)\": \"2128.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"519.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.24e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1780.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.095\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00147\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-45.0\", \"ZT\": \"0.05\", \"formula\": \"Sr1Nd0.2Ti0.8O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.83\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3484.0\", \"HHI (reserves)\": \"2153.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"678.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000137\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2020.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.137\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00181\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-32.0\", \"ZT\": \"0.02\", \"formula\": \"Sr1Nd0.24Ti0.76O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.29\", \"Average atomic mass (g/mol)\": \"41.32\", \"Scarcity (wt fraction/abundance)\": \"5689.0\", \"HHI (production)\": \"3673.0\", \"HHI (reserves)\": \"2186.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"553.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.49e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"992.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.102\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00267\", \"Seebeck coefficient (\\u03bcCV/K)\": \"148.0\", \"ZT\": \"0.33\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 0.9893245082, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.74\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"375.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000824\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.494\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00247\", \"Seebeck coefficient (\\u03bcCV/K)\": \"155.0\", \"ZT\": \"0.39\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 1.1700027838, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.743\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"405.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000975\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"24100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.533\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00251\", \"Seebeck coefficient (\\u03bcCV/K)\": \"161.0\", \"ZT\": \"0.41\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 1.2393625318, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.75\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"399.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00103\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.519\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.389\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-294.0\", \"ZT\": \"0.00888\", \"formula\": \"Zn1O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"33.22\", \"Average atomic mass (g/mol)\": \"40.69\", \"Scarcity (wt fraction/abundance)\": \"10780.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1621.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.25\", \"Power Factor (W/(K\\u00b2m))\": \"2.22e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"86400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"7.33e-06\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00617\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-191.0\", \"ZT\": \"0.24\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.7069753193, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"30.21\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"149.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000589\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0048\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00339\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-204.0\", \"ZT\": \"0.49\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.4741426266, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"30.21\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"254.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00123\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"41600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00819\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00129\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-148.0\", \"ZT\": \"0.68\", \"formula\": \"Zn0.98Al0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 2.0308211577, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"27.2\", \"Average atomic mass (g/mol)\": \"40.31\", \"Scarcity (wt fraction/abundance)\": \"10670.0\", \"HHI (production)\": \"1361.0\", \"HHI (reserves)\": \"1612.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"704.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00169\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.025\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00155\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-174.0\", \"ZT\": \"0.78\", \"formula\": \"Zn0.95Al0.05O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 2.3407808119, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"20.25\", \"Average atomic mass (g/mol)\": \"39.73\", \"Scarcity (wt fraction/abundance)\": \"10490.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1599.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"569.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00195\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.027\"}, {\"doi\": \"10.1016/j.jallcom.2010.06.195\", \"Electrical resistivity (\\u03a9cm)\": \"0.375\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-48.0\", \"ZT\": \"0.000241\", \"formula\": \"Sr1Nb0.15Ti0.85O3\", \"comment\": \"*Values at 1000K extrapolated from 900K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wang 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.696\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"5257.0\", \"HHI (production)\": \"2915.0\", \"HHI (reserves)\": \"2484.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.663\", \"Power Factor (W/(K\\u00b2m))\": \"6.02e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2260.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000554\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.00076\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-56.0\", \"ZT\": \"0.16\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"Czochralski method, He\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.4948042737, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.63\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1320.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000412\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3130.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.788\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.0009\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-62.0\", \"ZT\": \"0.17\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.51518208, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.42\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1110.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000429\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3860.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.764\"}, {\"doi\": \"10.1063/1.2163979\", \"Electrical resistivity (\\u03a9cm)\": \"0.000791\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-75.0\", \"ZT\": \"0.28\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"Czochralski method, argon\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Saramat 2006\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.8533501896, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.79\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1260.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000711\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.689\"}, {\"doi\": \"10.1103/PhysRevLett.86.4350\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"338.0\", \"ZT\": \"0.41\", \"formula\": \"Tl9Bi1Te6\", \"comment\": \"\", \"synthesis\": \"melted, zone refined\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wolfing 2001\", \"Structure\": \"ICSD #400246, 300K\", \"marker\": \"{'radius': 1.2266042256, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.409\", \"Average atomic mass (g/mol)\": \"175.88\", \"Scarcity (wt fraction/abundance)\": \"277400000.0\", \"HHI (production)\": \"5429.0\", \"HHI (reserves)\": \"6036.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1025.05\", \"Average atomic volume (\\u212b\\u00b3)\": \"32.033\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"89.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.00102\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"114000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.214\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.000499\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-55.0\", \"ZT\": \"0.24\", \"formula\": \"Bi1.2S1.2Ti2S4\", \"comment\": \"\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 0.7234923848, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.41\", \"Average atomic mass (g/mol)\": \"61.1\", \"Scarcity (wt fraction/abundance)\": \"28740000.0\", \"HHI (production)\": \"3036.0\", \"HHI (reserves)\": \"3543.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000603\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3010.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.812\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.000728\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-71.0\", \"ZT\": \"0.28\", \"formula\": \"Pb1.8S1.8Ti2S4\", \"comment\": \"\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 0.8262593407, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.51\", \"Average atomic mass (g/mol)\": \"68.19\", \"Scarcity (wt fraction/abundance)\": \"48160.0\", \"HHI (production)\": \"1920.0\", \"HHI (reserves)\": \"1526.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1370.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000689\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5010.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.534\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.00085\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.37\", \"formula\": \"Sn1.2S1.2Ti2S4\", \"comment\": \"\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 1.1132385882, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.03\", \"Average atomic mass (g/mol)\": \"48.21\", \"Scarcity (wt fraction/abundance)\": \"157400.0\", \"HHI (production)\": \"1480.0\", \"HHI (reserves)\": \"1355.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1180.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000928\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7890.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.566\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.00342\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-118.0\", \"ZT\": \"0.16\", \"formula\": \"Ba8Au5.14Si39.51\", \"comment\": \"\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"400\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 0.4893898246, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.61\", \"Average atomic mass (g/mol)\": \"61.17\", \"Scarcity (wt fraction/abundance)\": \"78590000.0\", \"HHI (production)\": \"2988.0\", \"HHI (reserves)\": \"1472.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"292.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000408\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.177\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.00253\", \"Seebeck coefficient (\\u03bcCV/K)\": \"126.0\", \"ZT\": \"0.25\", \"formula\": \"Ba8Au5.59Si39.01\", \"comment\": \"\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"400\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 0.759, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.62\", \"Average atomic mass (g/mol)\": \"62.65\", \"Scarcity (wt fraction/abundance)\": \"83530000.0\", \"HHI (production)\": \"2930.0\", \"HHI (reserves)\": \"1462.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"395.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000632\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.238\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.000702\", \"Seebeck coefficient (\\u03bcCV/K)\": \"57.0\", \"ZT\": \"0.19\", \"formula\": \"Ba8Au6.10Si38.97\", \"comment\": \"\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"400\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 0.5551897607, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.33\", \"Average atomic mass (g/mol)\": \"63.97\", \"Scarcity (wt fraction/abundance)\": \"88490000.0\", \"HHI (production)\": \"2876.0\", \"HHI (reserves)\": \"1450.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1420.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000463\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3250.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.597\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.00171\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-164.0\", \"ZT\": \"0.63\", \"formula\": \"Mg2Si0.999Bi0.001\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.9011038687, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.7\", \"Average atomic mass (g/mol)\": \"25.63\", \"Scarcity (wt fraction/abundance)\": \"159900.0\", \"HHI (production)\": \"5058.0\", \"HHI (reserves)\": \"697.4\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"586.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00158\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.1\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000902\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-149.0\", \"ZT\": \"0.98\", \"formula\": \"Mg2Si0.9985Bi0.0015\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 2.9535698448, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.07\", \"Average atomic mass (g/mol)\": \"25.66\", \"Scarcity (wt fraction/abundance)\": \"239600.0\", \"HHI (production)\": \"5058.0\", \"HHI (reserves)\": \"704.6\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1110.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00246\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.213\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000541\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.75\", \"formula\": \"Mg2Si0.997Bi0.003\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 2.2626987061, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.76\", \"Average atomic mass (g/mol)\": \"25.75\", \"Scarcity (wt fraction/abundance)\": \"477500.0\", \"HHI (production)\": \"5060.0\", \"HHI (reserves)\": \"725.9\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1850.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00189\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.379\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000396\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-84.0\", \"ZT\": \"0.7\", \"formula\": \"Mg2Si0.995Bi0.005\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 2.1128030303, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.41\", \"Average atomic mass (g/mol)\": \"25.87\", \"Scarcity (wt fraction/abundance)\": \"792100.0\", \"HHI (production)\": \"5061.0\", \"HHI (reserves)\": \"754.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2530.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00176\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6970.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.456\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000348\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-79.0\", \"ZT\": \"0.71\", \"formula\": \"Mg2Si0.993Bi0.007\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 2.1303310345, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.68\", \"Average atomic mass (g/mol)\": \"25.99\", \"Scarcity (wt fraction/abundance)\": \"1104000.0\", \"HHI (production)\": \"5063.0\", \"HHI (reserves)\": \"781.9\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2870.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00178\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6180.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.494\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.00121\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-110.0\", \"ZT\": \"0.4\", \"formula\": \"Mg2Si0.98Bi0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.2065543802, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.63\", \"Average atomic mass (g/mol)\": \"26.77\", \"Scarcity (wt fraction/abundance)\": \"3061000.0\", \"HHI (production)\": \"5072.0\", \"HHI (reserves)\": \"957.2\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"826.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00101\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.143\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.00127\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-118.0\", \"ZT\": \"0.43\", \"formula\": \"Mg2Si0.6Ge0.4Bi0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 1.3045275591, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.62\", \"Average atomic mass (g/mol)\": \"32.68\", \"Scarcity (wt fraction/abundance)\": \"2694000.0\", \"HHI (production)\": \"5169.0\", \"HHI (reserves)\": \"1229.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"787.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00109\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.293\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.413\", \"Seebeck coefficient (\\u03bcCV/K)\": \"178.0\", \"ZT\": \"0.00307\", \"formula\": \"Mg2Si0.98Ag0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"6.06\", \"Average atomic mass (g/mol)\": \"26.1\", \"Scarcity (wt fraction/abundance)\": \"353300.0\", \"HHI (production)\": \"4954.0\", \"HHI (reserves)\": \"699.7\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.421\", \"Power Factor (W/(K\\u00b2m))\": \"7.67e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00039\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"158.0\", \"ZT\": \"0.04\", \"formula\": \"Mg2Si0.6Ge0.4Ag0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.09\", \"Average atomic mass (g/mol)\": \"32.01\", \"Scarcity (wt fraction/abundance)\": \"493400.0\", \"HHI (production)\": \"5075.0\", \"HHI (reserves)\": \"1026.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"35.2\", \"Power Factor (W/(K\\u00b2m))\": \"8.78e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"24900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.011\"}, {\"doi\": \"10.1063/1.2009828\", \"Electrical resistivity (\\u03a9cm)\": \"0.083\", \"Seebeck coefficient (\\u03bcCV/K)\": \"327.0\", \"ZT\": \"0.05\", \"formula\": \"Ag9Tl1Te5\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kurosaki 2005\", \"Structure\": \"ICSD #71689, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.21\", \"Average atomic mass (g/mol)\": \"120.88\", \"Scarcity (wt fraction/abundance)\": \"358900000.0\", \"HHI (production)\": \"2408.0\", \"HHI (reserves)\": \"3201.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"4758.66\", \"Average atomic volume (\\u212b\\u00b3)\": \"27.349\", \"Atoms per unit cell\": \"174.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"12.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000129\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"107000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.056\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00305\", \"Seebeck coefficient (\\u03bcCV/K)\": \"185.0\", \"ZT\": \"0.45\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"*kappa extrapolated\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 1.3469990161, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"328.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00112\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.16\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00714\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-113.0\", \"ZT\": \"0.07\", \"formula\": \"Ba8Ga18Ge28\", \"comment\": \"\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.4\", \"Average atomic mass (g/mol)\": \"81.25\", \"Scarcity (wt fraction/abundance)\": \"335300.0\", \"HHI (production)\": \"4759.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"140.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000178\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.098\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-233.0\", \"ZT\": \"0.19\", \"formula\": \"Ba8Ga16Sn30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #161949, 300K\", \"marker\": \"{'radius': 0.566493913, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"106.95\", \"Scarcity (wt fraction/abundance)\": \"284700.0\", \"HHI (production)\": \"3226.0\", \"HHI (reserves)\": \"1823.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1595.46\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.546\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"87.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000472\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"54300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.000914\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-95.0\", \"ZT\": \"0.39\", \"formula\": \"Sr8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #90177, 295K\", \"marker\": \"{'radius': 1.1824083151, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"73.99\", \"Scarcity (wt fraction/abundance)\": \"391300.0\", \"HHI (production)\": \"5141.0\", \"HHI (reserves)\": \"2089.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1233.18\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.837\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1090.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000985\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9010.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.00084\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.48\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 1.45152, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1190.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00121\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.00133\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-63.0\", \"ZT\": \"0.12\", \"formula\": \"Ba8Ga16Si30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 0.355835188, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.61\", \"Scarcity (wt fraction/abundance)\": \"20060.0\", \"HHI (production)\": \"4373.0\", \"HHI (reserves)\": \"1811.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"752.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000297\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3940.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00198\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-189.0\", \"ZT\": \"0.72\", \"formula\": \"Mg2Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 2.169291498, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.0\", \"Average atomic mass (g/mol)\": \"25.57\", \"Scarcity (wt fraction/abundance)\": \"27.34\", \"HHI (production)\": \"5057.0\", \"HHI (reserves)\": \"683.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"506.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00181\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.123\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00115\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-95.0\", \"ZT\": \"0.31\", \"formula\": \"Mg1.95Ca0.05Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.937778087, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.9\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"27.02\", \"HHI (production)\": \"5023.0\", \"HHI (reserves)\": \"707.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"870.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000781\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8990.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.173\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00214\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-74.0\", \"ZT\": \"0.1\", \"formula\": \"Mg1.9Ca0.1Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.3069219991, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.7\", \"Average atomic mass (g/mol)\": \"26.09\", \"Scarcity (wt fraction/abundance)\": \"26.71\", \"HHI (production)\": \"4990.0\", \"HHI (reserves)\": \"730.6\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"467.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000256\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5480.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.097\"}, {\"doi\": \"10.1016/j.jcrysgro.2006.10.270\", \"Electrical resistivity (\\u03a9cm)\": \"0.00173\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-205.0\", \"ZT\": \"0.97\", \"formula\": \"Mg2Si1\", \"comment\": \"\", \"synthesis\": \"Bridgman method, Ar-H gas\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Akasaka 2007\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 2.9150289017, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"6.15\", \"Average atomic mass (g/mol)\": \"25.57\", \"Scarcity (wt fraction/abundance)\": \"27.34\", \"HHI (production)\": \"5057.0\", \"HHI (reserves)\": \"683.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"578.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00243\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.092\"}, {\"doi\": \"10.1038/nmat3274\", \"Electrical resistivity (\\u03a9cm)\": \"0.00161\", \"Seebeck coefficient (\\u03bcCV/K)\": \"107.0\", \"ZT\": \"0.28\", \"formula\": \"Cu2Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 0.8533416149, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.04\", \"Average atomic mass (g/mol)\": \"68.68\", \"Scarcity (wt fraction/abundance)\": \"7674000.0\", \"HHI (production)\": \"1825.0\", \"HHI (reserves)\": \"1672.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"621.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000711\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.583\"}, {\"doi\": \"10.1038/nmat3278\", \"Electrical resistivity (\\u03a9cm)\": \"0.000719\", \"Seebeck coefficient (\\u03bcCV/K)\": \"64.0\", \"ZT\": \"0.23\", \"formula\": \"Cu1.98Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 0.6878954103, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.73\", \"Average atomic mass (g/mol)\": \"68.72\", \"Scarcity (wt fraction/abundance)\": \"7721000.0\", \"HHI (production)\": \"1826.0\", \"HHI (reserves)\": \"1673.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1390.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000573\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4120.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.785\"}, {\"doi\": \"http://link.aip.org/link/doi/10.1063/1.1562337\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"152.0\", \"ZT\": \"0.43\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"flux (SrCl2), air\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Shikano 2003\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 1.2764640884, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"3.444\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"460.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00106\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.13\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"121.0\", \"ZT\": \"0.05\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.9\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"89.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.00013\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.046\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00529\", \"Seebeck coefficient (\\u03bcCV/K)\": \"126.0\", \"ZT\": \"0.12\", \"formula\": \"Ca2.7Na0.3Co4O9\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.357582773, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.9\", \"Average atomic mass (g/mol)\": \"30.93\", \"Scarcity (wt fraction/abundance)\": \"17330.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1745.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"189.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000298\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.097\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"141.0\", \"ZT\": \"0.08\", \"formula\": \"Ca2.7Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.9\", \"Average atomic mass (g/mol)\": \"34.41\", \"Scarcity (wt fraction/abundance)\": \"6713000.0\", \"HHI (production)\": \"2799.0\", \"HHI (reserves)\": \"2245.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"98.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000195\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.051\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00922\", \"Seebeck coefficient (\\u03bcCV/K)\": \"145.0\", \"ZT\": \"0.09\", \"formula\": \"Ca2.4Na0.3Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.9\", \"Average atomic mass (g/mol)\": \"34.09\", \"Scarcity (wt fraction/abundance)\": \"6776000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2239.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"108.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000227\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.056\"}, {\"doi\": \"http://jjap.jsap.jp/link?JJAP/43/L540/\", \"Electrical resistivity (\\u03a9cm)\": \"0.00126\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-120.0\", \"ZT\": \"0.45\", \"formula\": \"Sr0.9Y0.1Ti1O3\", \"comment\": \"*kappa estimated from  300K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Obara 2004\", \"Structure\": \"ICSD #181231, 300K\", \"marker\": \"{'radius': 1.3611040508, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"6.0\", \"Average atomic mass (g/mol)\": \"36.72\", \"Scarcity (wt fraction/abundance)\": \"2782.0\", \"HHI (production)\": \"2693.0\", \"HHI (reserves)\": \"1952.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.872\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"794.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00113\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.129\"}, {\"doi\": \"10.1016/j.jallcom.2003.07.016\", \"Electrical resistivity (\\u03a9cm)\": \"0.000763\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.54\", \"formula\": \"Ba0.3Sr0.6La0.1Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction , Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2004\", \"Structure\": \"ICSD #181231, 300K\", \"marker\": \"{'radius': 1.6162368352, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.36\", \"Average atomic mass (g/mol)\": \"40.7\", \"Scarcity (wt fraction/abundance)\": \"3096.0\", \"HHI (production)\": \"2709.0\", \"HHI (reserves)\": \"1946.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.872\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1310.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00135\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.381\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.219\", \"Seebeck coefficient (\\u03bcCV/K)\": \"275.0\", \"ZT\": \"0.01\", \"formula\": \"Cu1Rh1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.61\", \"Scarcity (wt fraction/abundance)\": \"518600000.0\", \"HHI (production)\": \"2265.0\", \"HHI (reserves)\": \"4717.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.56\", \"Power Factor (W/(K\\u00b2m))\": \"3.46e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"75800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.066\", \"Seebeck coefficient (\\u03bcCV/K)\": \"259.0\", \"ZT\": \"0.04\", \"formula\": \"Cu1Rh0.99Mg0.01O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.42\", \"Scarcity (wt fraction/abundance)\": \"515400000.0\", \"HHI (production)\": \"2263.0\", \"HHI (reserves)\": \"4695.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"15.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000102\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"67100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"188.0\", \"ZT\": \"0.13\", \"formula\": \"Cu1Rh0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.3778804286, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.83\", \"Scarcity (wt fraction/abundance)\": \"505800000.0\", \"HHI (production)\": \"2259.0\", \"HHI (reserves)\": \"4627.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"89.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000315\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.00196\", \"Seebeck coefficient (\\u03bcCV/K)\": \"115.0\", \"ZT\": \"0.27\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.8096938776, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"510.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000675\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.538\", \"Seebeck coefficient (\\u03bcCV/K)\": \"316.0\", \"ZT\": \"0.00743\", \"formula\": \"Ca3Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.1\", \"Average atomic mass (g/mol)\": \"73.21\", \"Scarcity (wt fraction/abundance)\": \"3564000.0\", \"HHI (production)\": \"6623.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1.86\", \"Power Factor (W/(K\\u00b2m))\": \"1.86e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"99800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00165\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.046\", \"Seebeck coefficient (\\u03bcCV/K)\": \"165.0\", \"ZT\": \"0.02\", \"formula\": \"Ca2.97Na0.03Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.24\", \"Average atomic mass (g/mol)\": \"73.14\", \"Scarcity (wt fraction/abundance)\": \"3567000.0\", \"HHI (production)\": \"6622.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.7\", \"Power Factor (W/(K\\u00b2m))\": \"5.89e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.017\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.034\", \"Seebeck coefficient (\\u03bcCV/K)\": \"150.0\", \"ZT\": \"0.03\", \"formula\": \"Ca2.94Na0.06Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.27\", \"Average atomic mass (g/mol)\": \"73.07\", \"Scarcity (wt fraction/abundance)\": \"3571000.0\", \"HHI (production)\": \"6621.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"29.7\", \"Power Factor (W/(K\\u00b2m))\": \"6.68e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.023\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"152.0\", \"ZT\": \"0.05\", \"formula\": \"Ca2.85Na0.15Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.24\", \"Average atomic mass (g/mol)\": \"72.85\", \"Scarcity (wt fraction/abundance)\": \"3582000.0\", \"HHI (production)\": \"6618.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"53.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000124\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.042\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-183.0\", \"ZT\": \"0.05\", \"formula\": \"Fe0.998Co0.002Si2\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.34\", \"Average atomic mass (g/mol)\": \"37.34\", \"Scarcity (wt fraction/abundance)\": \"48.87\", \"HHI (production)\": \"3570.0\", \"HHI (reserves)\": \"1187.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"38.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000129\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"33500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00703\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.056\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-327.0\", \"ZT\": \"0.08\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.04O0.06\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.09\", \"Average atomic mass (g/mol)\": \"37.6\", \"Scarcity (wt fraction/abundance)\": \"1051.0\", \"HHI (production)\": \"3739.0\", \"HHI (reserves)\": \"1227.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"17.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.00019\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"107000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00424\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.15\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-227.0\", \"ZT\": \"0.01\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.12O0.18\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.64\", \"Average atomic mass (g/mol)\": \"38.06\", \"Scarcity (wt fraction/abundance)\": \"2834.0\", \"HHI (production)\": \"4040.0\", \"HHI (reserves)\": \"1297.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"6.689\", \"Power Factor (W/(K\\u00b2m))\": \"3.45e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"51500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00247\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.409\", \"Seebeck coefficient (\\u03bcCV/K)\": \"463.0\", \"ZT\": \"0.02\", \"formula\": \"Ca5Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.23\", \"Average atomic mass (g/mol)\": \"75.76\", \"Scarcity (wt fraction/abundance)\": \"3709000.0\", \"HHI (production)\": \"6736.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.445\", \"Power Factor (W/(K\\u00b2m))\": \"5.24e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"214000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00194\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"220.0\", \"ZT\": \"0.09\", \"formula\": \"Ca4.95Na0.05Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.2\", \"Average atomic mass (g/mol)\": \"75.7\", \"Scarcity (wt fraction/abundance)\": \"3712000.0\", \"HHI (production)\": \"6735.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"44.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000216\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.036\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.00544\", \"Seebeck coefficient (\\u03bcCV/K)\": \"161.0\", \"ZT\": \"0.19\", \"formula\": \"Ca4.75Na0.25Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.5717867647, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.16\", \"Average atomic mass (g/mol)\": \"75.43\", \"Scarcity (wt fraction/abundance)\": \"3725000.0\", \"HHI (production)\": \"6732.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"184.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000476\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.155\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.492\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-403.0\", \"ZT\": \"0.01\", \"formula\": \"Fe1.98Ti0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.91\", \"Scarcity (wt fraction/abundance)\": \"13.87\", \"HHI (production)\": \"1837.0\", \"HHI (reserves)\": \"1111.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"20300.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.3e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"162000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.214\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-344.0\", \"ZT\": \"0.02\", \"formula\": \"Fe1.96Ti0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.87\", \"Average atomic mass (g/mol)\": \"31.87\", \"Scarcity (wt fraction/abundance)\": \"14.74\", \"HHI (production)\": \"1829.0\", \"HHI (reserves)\": \"1112.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46700.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.53e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"118000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"6.641\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.206\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-309.0\", \"ZT\": \"0.02\", \"formula\": \"Fe1.94Ti0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.93\", \"Average atomic mass (g/mol)\": \"31.84\", \"Scarcity (wt fraction/abundance)\": \"15.62\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"1113.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"48600.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.63e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"95300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"7.994\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.515\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-413.0\", \"ZT\": \"0.01\", \"formula\": \"Fe1.98Sn0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.19\", \"Scarcity (wt fraction/abundance)\": \"6569.0\", \"HHI (production)\": \"1853.0\", \"HHI (reserves)\": \"1117.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"19400.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.32e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"171000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.263\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-336.0\", \"ZT\": \"0.02\", \"formula\": \"Fe1.96Sn0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.17\", \"Average atomic mass (g/mol)\": \"32.44\", \"Scarcity (wt fraction/abundance)\": \"13020.0\", \"HHI (production)\": \"1860.0\", \"HHI (reserves)\": \"1122.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"38000.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.27e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"113000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"6.005\"}, {\"doi\": \"10.1016/j.jssc.2011.02.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.00066\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-34.0\", \"ZT\": \"0.07\", \"formula\": \"Ba7Sr1Al16Si30\", \"comment\": \"\", \"synthesis\": \"flux (Al), dynamic vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Roudebush 2011\", \"Structure\": \"ICSD #380509, 90K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.33\", \"Average atomic mass (g/mol)\": \"43.02\", \"Scarcity (wt fraction/abundance)\": \"1088.0\", \"HHI (production)\": \"3387.0\", \"HHI (reserves)\": \"1633.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1193.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.691\", \"Atoms per unit cell\": \"55.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1510.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000172\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1140.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.634\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"2.162\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-618.0\", \"ZT\": \"0.00708\", \"formula\": \"Nd2Cu1O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"13.7\", \"Average atomic mass (g/mol)\": \"59.43\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6889.0\", \"HHI (reserves)\": \"2479.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.463\", \"Power Factor (W/(K\\u00b2m))\": \"1.77e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"382000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"3.3e-05\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.038\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-183.0\", \"ZT\": \"0.03\", \"formula\": \"Nd2Cu0.98Ni0.02O4\", \"comment\": \"*kappa extrapolated from 325 K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"8.03\", \"Average atomic mass (g/mol)\": \"59.42\", \"Scarcity (wt fraction/abundance)\": \"20980.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2480.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"26.1\", \"Power Factor (W/(K\\u00b2m))\": \"8.72e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"33400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00318\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.141\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-294.0\", \"ZT\": \"0.02\", \"formula\": \"Nd2Cu0.98Zn0.02O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"11.1\", \"Average atomic mass (g/mol)\": \"59.44\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2481.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"7.115\", \"Power Factor (W/(K\\u00b2m))\": \"6.17e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"86700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000626\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.000589\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-47.0\", \"ZT\": \"0.15\", \"formula\": \"La3Te3.8Sb0.2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.44242309, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.58\", \"Average atomic mass (g/mol)\": \"132.28\", \"Scarcity (wt fraction/abundance)\": \"523800000.0\", \"HHI (production)\": \"5987.0\", \"HHI (reserves)\": \"4082.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1700.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000369\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2170.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.642\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00137\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-58.0\", \"ZT\": \"0.1\", \"formula\": \"La3Te3.65Sb0.35\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.06\", \"Average atomic mass (g/mol)\": \"132.15\", \"Scarcity (wt fraction/abundance)\": \"503700000.0\", \"HHI (production)\": \"6089.0\", \"HHI (reserves)\": \"4051.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"730.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000246\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3360.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.346\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00135\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-90.0\", \"ZT\": \"0.24\", \"formula\": \"La3Te3.35Sb0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.7184008889, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.36\", \"Average atomic mass (g/mol)\": \"131.9\", \"Scarcity (wt fraction/abundance)\": \"463400000.0\", \"HHI (production)\": \"6293.0\", \"HHI (reserves)\": \"3990.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"741.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000599\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8080.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.532\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00535\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-70.0\", \"ZT\": \"0.04\", \"formula\": \"La3Te3.35Bi0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.83\", \"Average atomic mass (g/mol)\": \"140.0\", \"Scarcity (wt fraction/abundance)\": \"444300000.0\", \"HHI (production)\": \"6025.0\", \"HHI (reserves)\": \"4313.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"187.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.03e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4830.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.1\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00061\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-42.0\", \"ZT\": \"0.11\", \"formula\": \"La2.99Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.3404380328, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.605\", \"Average atomic mass (g/mol)\": \"132.44\", \"Scarcity (wt fraction/abundance)\": \"551400000.0\", \"HHI (production)\": \"5846.0\", \"HHI (reserves)\": \"4124.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1640.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000284\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1730.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.614\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00268\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.12\", \"formula\": \"La2.74Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.3546716418, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.17\", \"Average atomic mass (g/mol)\": \"132.2\", \"Scarcity (wt fraction/abundance)\": \"572900000.0\", \"HHI (production)\": \"5704.0\", \"HHI (reserves)\": \"4163.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"373.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000296\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7920.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.311\"}, {\"doi\": \"10.1021/nl202439h\", \"Electrical resistivity (\\u03a9cm)\": \"0.195\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-220.0\", \"ZT\": \"0.00995\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"microwave solvothermal, air\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Jood 2011\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.687\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5.14\", \"Power Factor (W/(K\\u00b2m))\": \"2.49e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00187\"}, {\"doi\": \"10.1063/1.3291563\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-194.0\", \"ZT\": \"0.1\", \"formula\": \"Sr0.61Ba0.39Nb2O6\", \"comment\": \"*kappa from Choy 1992 polycrystalline samples used, values parallel to c axis\", \"synthesis\": \"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\", \"form\": \"single crystal\", \"temperature\": \"400\", \"author\": \"Lee 2010\", \"Structure\": \"ICSD #96013, 300K\", \"marker\": \"{'radius': 0.3090482776, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.02\", \"Average atomic mass (g/mol)\": \"43.2\", \"Scarcity (wt fraction/abundance)\": \"26540.0\", \"HHI (production)\": \"5182.0\", \"HHI (reserves)\": \"5061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"610.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.564\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"68.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000258\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"37600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.033\"}, {\"doi\": \"10.1557/jmr.2010.78\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-220.0\", \"ZT\": \"0.12\", \"formula\": \"Sr0.61Ba0.39Nb2O6\", \"comment\": \"*kappa from Choy 1992 polycrystalline samples used, values parallel to c axis\", \"synthesis\": \"templated grain growth, air, anneal PO<sub>2</sub> 10<sup>-14</sup>\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Lee 2011\", \"Structure\": \"ICSD #96013, 300K\", \"marker\": \"{'radius': 0.35794704, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.02\", \"Average atomic mass (g/mol)\": \"43.2\", \"Scarcity (wt fraction/abundance)\": \"26540.0\", \"HHI (production)\": \"5182.0\", \"HHI (reserves)\": \"5061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"610.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.564\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"61.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000298\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.03\"}, {\"doi\": \"10.1021/nl8026795\", \"Electrical resistivity (\\u03a9cm)\": \"0.00129\", \"Seebeck coefficient (\\u03bcCV/K)\": \"138.0\", \"ZT\": \"0.59\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"ball milling, hot-pressed nanopowders\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Joshi 2008\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 1.779997205, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"2.52\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"774.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00148\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.3\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.000845\", \"Seebeck coefficient (\\u03bcCV/K)\": \"128.0\", \"ZT\": \"0.78\", \"formula\": \"Pb0.96Sr0.4Te1Na0.2\", \"comment\": \"\", \"synthesis\": \"sparks plasma sintering\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 2.32783872, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.126\", \"Average atomic mass (g/mol)\": \"143.03\", \"Scarcity (wt fraction/abundance)\": \"348500000.0\", \"HHI (production)\": \"2897.0\", \"HHI (reserves)\": \"2980.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1180.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.544\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.000707\", \"Seebeck coefficient (\\u03bcCV/K)\": \"117.0\", \"ZT\": \"0.77\", \"formula\": \"Pb0.98Sr0.2Te1Na0.1\", \"comment\": \"\", \"synthesis\": \"melting\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 2.3243922, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.23\", \"Average atomic mass (g/mol)\": \"153.72\", \"Scarcity (wt fraction/abundance)\": \"364100000.0\", \"HHI (production)\": \"2843.0\", \"HHI (reserves)\": \"2981.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1420.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.619\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.000576\", \"Seebeck coefficient (\\u03bcCV/K)\": \"105.0\", \"ZT\": \"0.77\", \"formula\": \"Pb0.98Te1Na0.2\", \"comment\": \"\", \"synthesis\": \"melting\", \"form\": \"polycrystalline\", \"temperature\": \"400\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 2.296728, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.18\", \"Average atomic mass (g/mol)\": \"153.79\", \"Scarcity (wt fraction/abundance)\": \"380700000.0\", \"HHI (production)\": \"2761.0\", \"HHI (reserves)\": \"2963.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1740.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00191\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.533\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"2.417\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-471.0\", \"ZT\": \"0.00641\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.414\", \"Power Factor (W/(K\\u00b2m))\": \"9.16e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"222000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.065\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-224.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.98La0.02Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82210, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.0\", \"Scarcity (wt fraction/abundance)\": \"917.3\", \"HHI (production)\": \"1996.0\", \"HHI (reserves)\": \"1310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.74\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.387\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"15.4\", \"Power Factor (W/(K\\u00b2m))\": \"7.72e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"50200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-174.0\", \"ZT\": \"0.1\", \"formula\": \"Ca0.96La0.04Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82209, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.39\", \"Scarcity (wt fraction/abundance)\": \"1423.0\", \"HHI (production)\": \"2128.0\", \"HHI (reserves)\": \"1343.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.49\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.424\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000139\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-127.0\", \"ZT\": \"0.07\", \"formula\": \"Ca0.94La0.06Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82208, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.79\", \"Scarcity (wt fraction/abundance)\": \"1915.0\", \"HHI (production)\": \"2255.0\", \"HHI (reserves)\": \"1376.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.24\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.462\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"58.7\", \"Power Factor (W/(K\\u00b2m))\": \"9.54e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-118.0\", \"ZT\": \"0.07\", \"formula\": \"Ca0.92La0.08Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82207, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"2394.0\", \"HHI (production)\": \"2380.0\", \"HHI (reserves)\": \"1407.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.497\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"73.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000103\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"153.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"483.0\", \"ZT\": \"0.000107\", \"formula\": \"Ni1O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.35\", \"Scarcity (wt fraction/abundance)\": \"6477.0\", \"HHI (production)\": \"883.5\", \"HHI (reserves)\": \"1269.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00654\", \"Power Factor (W/(K\\u00b2m))\": \"1.53e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"234000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.263\", \"Seebeck coefficient (\\u03bcCV/K)\": \"250.0\", \"ZT\": \"0.02\", \"formula\": \"Li0.0024Ni0.9976O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"11.391\", \"Average atomic mass (g/mol)\": \"37.28\", \"Scarcity (wt fraction/abundance)\": \"6484.0\", \"HHI (production)\": \"883.7\", \"HHI (reserves)\": \"1270.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.804\", \"Power Factor (W/(K\\u00b2m))\": \"2.37e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"62400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00057\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.032\", \"Seebeck coefficient (\\u03bcCV/K)\": \"200.0\", \"ZT\": \"0.09\", \"formula\": \"Li0.0066Ni0.9944O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.01\", \"Average atomic mass (g/mol)\": \"37.19\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"884.2\", \"HHI (reserves)\": \"1270.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"31.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000127\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00899\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.02\", \"Seebeck coefficient (\\u03bcCV/K)\": \"98.0\", \"ZT\": \"0.03\", \"formula\": \"Li0.0184Ni0.9816O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"36.87\", \"Scarcity (wt fraction/abundance)\": \"6533.0\", \"HHI (production)\": \"885.3\", \"HHI (reserves)\": \"1271.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"50.5\", \"Power Factor (W/(K\\u00b2m))\": \"4.84e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9580.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.00487\", \"Seebeck coefficient (\\u03bcCV/K)\": \"77.0\", \"ZT\": \"0.09\", \"formula\": \"Li0.0242Ni0.9758O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.496\", \"Average atomic mass (g/mol)\": \"36.72\", \"Scarcity (wt fraction/abundance)\": \"6552.0\", \"HHI (production)\": \"885.9\", \"HHI (reserves)\": \"1272.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"206.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000123\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5990.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.1\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.643\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-477.0\", \"ZT\": \"0.02\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.047\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1.555\", \"Power Factor (W/(K\\u00b2m))\": \"3.54e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"228000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0013\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-184.0\", \"ZT\": \"0.09\", \"formula\": \"Ca0.98Bi0.02Mn0.98Nb0.02O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.878\", \"Average atomic mass (g/mol)\": \"29.43\", \"Scarcity (wt fraction/abundance)\": \"1672000.0\", \"HHI (production)\": \"2034.0\", \"HHI (reserves)\": \"1500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"38.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000131\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.035\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-164.0\", \"ZT\": \"0.15\", \"formula\": \"Ca0.96Bi0.04Mn0.96Nb0.04O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.4522318823, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.878\", \"Average atomic mass (g/mol)\": \"30.26\", \"Scarcity (wt fraction/abundance)\": \"3252000.0\", \"HHI (production)\": \"2198.0\", \"HHI (reserves)\": \"1711.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"80.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000215\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.073\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.00763\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-81.0\", \"ZT\": \"0.06\", \"formula\": \"Ca0.9Bi0.1Mn0.9Nb0.1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.74\", \"Scarcity (wt fraction/abundance)\": \"7513000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"2282.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"131.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.52e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/jmr.2011.140\", \"Electrical resistivity (\\u03a9cm)\": \"0.028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-235.0\", \"ZT\": \"0.14\", \"formula\": \"Ca1Mn0.98Nb0.02O3\", \"comment\": \"\", \"synthesis\": \"Ultrasonic Spray Pyrolysis\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Populoh 2011\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.4074773224, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.631\", \"Average atomic mass (g/mol)\": \"28.75\", \"Scarcity (wt fraction/abundance)\": \"1087.0\", \"HHI (production)\": \"1950.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"35.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"55000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.037\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.024\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-196.0\", \"ZT\": \"0.11\", \"formula\": \"Ca1Mn0.98Ru0.02O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.332862836, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.79\", \"Scarcity (wt fraction/abundance)\": \"14040000.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"1366.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"41.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000159\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-137.0\", \"ZT\": \"0.13\", \"formula\": \"Ca1Mn0.96Ru0.04O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.388273783, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.24\", \"Average atomic mass (g/mol)\": \"28.97\", \"Scarcity (wt fraction/abundance)\": \"27910000.0\", \"HHI (production)\": \"1904.0\", \"HHI (reserves)\": \"1456.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"98.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000185\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.052\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00892\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-122.0\", \"ZT\": \"0.12\", \"formula\": \"Ca1Mn0.94Ru0.06O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.3515467057, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.16\", \"Scarcity (wt fraction/abundance)\": \"41600000.0\", \"HHI (production)\": \"1925.0\", \"HHI (reserves)\": \"1544.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"112.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000167\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00529\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-82.0\", \"ZT\": \"0.09\", \"formula\": \"Ca1Mn0.9Ru0.1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.53\", \"Scarcity (wt fraction/abundance)\": \"68460000.0\", \"HHI (production)\": \"1966.0\", \"HHI (reserves)\": \"1717.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"189.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000126\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6660.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00403\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-56.0\", \"ZT\": \"0.05\", \"formula\": \"Ca1Mn0.82Ru0.18O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.26\", \"Scarcity (wt fraction/abundance)\": \"120200000.0\", \"HHI (production)\": \"2045.0\", \"HHI (reserves)\": \"2051.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"248.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.75e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3120.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-228.0\", \"ZT\": \"0.16\", \"formula\": \"Ca1Gd0.98Mn0.02O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.4935015527, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.66\", \"Scarcity (wt fraction/abundance)\": \"111100.0\", \"HHI (production)\": \"6744.0\", \"HHI (reserves)\": \"2336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"45.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000235\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"51900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-173.0\", \"ZT\": \"0.18\", \"formula\": \"Ca1Gd0.96Mn0.04O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.5365444944, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.346\", \"Average atomic mass (g/mol)\": \"48.25\", \"Scarcity (wt fraction/abundance)\": \"109800.0\", \"HHI (production)\": \"6685.0\", \"HHI (reserves)\": \"2323.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"85.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000255\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.109\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.00866\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-145.0\", \"ZT\": \"0.17\", \"formula\": \"Ca1Gd0.94Mn0.06O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.5079513856, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.139\", \"Average atomic mass (g/mol)\": \"47.84\", \"Scarcity (wt fraction/abundance)\": \"108400.0\", \"HHI (production)\": \"6625.0\", \"HHI (reserves)\": \"2310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"115.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000242\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.092\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00193\", \"Seebeck coefficient (\\u03bcCV/K)\": \"32.0\", \"ZT\": \"0.04\", \"formula\": \"Nd1.4Bi0.6Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78129, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"58.31\", \"Scarcity (wt fraction/abundance)\": \"326600000.0\", \"HHI (production)\": \"5126.0\", \"HHI (reserves)\": \"4765.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1102.66\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.53\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"519.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.46e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1050.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00134\", \"Seebeck coefficient (\\u03bcCV/K)\": \"30.0\", \"ZT\": \"0.05\", \"formula\": \"Nd1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"60.67\", \"Scarcity (wt fraction/abundance)\": \"321300000.0\", \"HHI (production)\": \"4772.0\", \"HHI (reserves)\": \"5060.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"746.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.83e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"915.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.0031\", \"Seebeck coefficient (\\u03bcCV/K)\": \"29.0\", \"ZT\": \"0.02\", \"formula\": \"Yb1.4Bi0.6Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"61.98\", \"Scarcity (wt fraction/abundance)\": \"307400000.0\", \"HHI (production)\": \"5384.0\", \"HHI (reserves)\": \"4668.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"323.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.77e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"860.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00177\", \"Seebeck coefficient (\\u03bcCV/K)\": \"29.0\", \"ZT\": \"0.03\", \"formula\": \"Yb1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"63.29\", \"Scarcity (wt fraction/abundance)\": \"308100000.0\", \"HHI (production)\": \"4966.0\", \"HHI (reserves)\": \"4980.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"565.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.86e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"860.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000574\", \"Seebeck coefficient (\\u03bcCV/K)\": \"5.0\", \"ZT\": \"0.00352\", \"formula\": \"Bi2Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73787, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"66.55\", \"Scarcity (wt fraction/abundance)\": \"309700000.0\", \"HHI (production)\": \"3994.0\", \"HHI (reserves)\": \"5707.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1090.63\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.394\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1730.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.03e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28.9\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00105\", \"Seebeck coefficient (\\u03bcCV/K)\": \"15.0\", \"ZT\": \"0.02\", \"formula\": \"Y0.5Bi1.5Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73790, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"61.1\", \"Scarcity (wt fraction/abundance)\": \"328200000.0\", \"HHI (production)\": \"4178.0\", \"HHI (reserves)\": \"5460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1079.79\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.27\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"946.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.22e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"234.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.0019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"17.0\", \"ZT\": \"0.01\", \"formula\": \"Y1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73793, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.64\", \"Scarcity (wt fraction/abundance)\": \"350400000.0\", \"HHI (production)\": \"4398.0\", \"HHI (reserves)\": \"5165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1069.75\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.156\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"515.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.55e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"294.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.284\", \"Seebeck coefficient (\\u03bcCV/K)\": \"22.0\", \"ZT\": \"0.000118\", \"formula\": \"Y2Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73799, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"44.72\", \"Scarcity (wt fraction/abundance)\": \"410900000.0\", \"HHI (production)\": \"4999.0\", \"HHI (reserves)\": \"4357.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1040.8\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.827\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.465\", \"Power Factor (W/(K\\u00b2m))\": \"1.69e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"480.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-124.0\", \"ZT\": \"0.06\", \"formula\": \"Ca0.9Nd0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164747, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.416\", \"Average atomic mass (g/mol)\": \"30.69\", \"Scarcity (wt fraction/abundance)\": \"2894.0\", \"HHI (production)\": \"2525.0\", \"HHI (reserves)\": \"1444.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.546\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"57.5\", \"Power Factor (W/(K\\u00b2m))\": \"8.81e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.041\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-124.0\", \"ZT\": \"0.07\", \"formula\": \"Ca0.9Tb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164751, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.756\", \"Average atomic mass (g/mol)\": \"30.98\", \"Scarcity (wt fraction/abundance)\": \"96250.0\", \"HHI (production)\": \"2591.0\", \"HHI (reserves)\": \"1460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.451\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"65.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.0001\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.063\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.00981\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-124.0\", \"ZT\": \"0.11\", \"formula\": \"Ca0.9Ho0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164753, 293K\", \"marker\": \"{'radius': 0.3282939172, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.185\", \"Average atomic mass (g/mol)\": \"31.1\", \"Scarcity (wt fraction/abundance)\": \"85220.0\", \"HHI (production)\": \"2618.0\", \"HHI (reserves)\": \"1467.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.422\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"102.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000156\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.08\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.00599\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-124.0\", \"ZT\": \"0.18\", \"formula\": \"Ca0.9Yb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 293K\", \"marker\": \"{'radius': 0.5376778296, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.609\", \"Average atomic mass (g/mol)\": \"31.26\", \"Scarcity (wt fraction/abundance)\": \"37270.0\", \"HHI (production)\": \"2653.0\", \"HHI (reserves)\": \"1475.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"167.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000256\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.177\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.233\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-375.0\", \"ZT\": \"0.04\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.165\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.29\", \"Power Factor (W/(K\\u00b2m))\": \"6.03e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"140000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00338\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00832\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-125.0\", \"ZT\": \"0.13\", \"formula\": \"Ca0.9Tb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69824, 300K\", \"marker\": \"{'radius': 0.3916823272, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.575\", \"Average atomic mass (g/mol)\": \"30.98\", \"Scarcity (wt fraction/abundance)\": \"96250.0\", \"HHI (production)\": \"2591.0\", \"HHI (reserves)\": \"1460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.479\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"120.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000187\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.13\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00526\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-55.0\", \"ZT\": \"0.04\", \"formula\": \"Ca0.7Tb0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69826, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.462\", \"Average atomic mass (g/mol)\": \"35.73\", \"Scarcity (wt fraction/abundance)\": \"249700.0\", \"HHI (production)\": \"3759.0\", \"HHI (reserves)\": \"1755.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.15\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.658\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"190.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.82e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3060.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.222\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.0095\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.08\", \"formula\": \"Ca0.9Ho0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160306, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.518\", \"Average atomic mass (g/mol)\": \"31.1\", \"Scarcity (wt fraction/abundance)\": \"85220.0\", \"HHI (production)\": \"2618.0\", \"HHI (reserves)\": \"1467.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.04\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.452\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"105.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000108\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.118\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00377\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-51.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.7Ho0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.417\", \"Average atomic mass (g/mol)\": \"36.09\", \"Scarcity (wt fraction/abundance)\": \"219600.0\", \"HHI (production)\": \"3816.0\", \"HHI (reserves)\": \"1769.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"265.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.9e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.32\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00592\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-113.0\", \"ZT\": \"0.15\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.4515653606, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.601\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"169.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000215\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.18\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00628\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-52.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.7Y0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #97601, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.515\", \"Average atomic mass (g/mol)\": \"31.53\", \"Scarcity (wt fraction/abundance)\": \"5816.0\", \"HHI (production)\": \"3058.0\", \"HHI (reserves)\": \"1490.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"219.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.992\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"159.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.38e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2750.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.18\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000527\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-34.0\", \"ZT\": \"0.15\", \"formula\": \"Ba1Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.4505466283, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.116\", \"Average atomic mass (g/mol)\": \"78.5\", \"Scarcity (wt fraction/abundance)\": \"44820.0\", \"HHI (production)\": \"2535.0\", \"HHI (reserves)\": \"1822.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1900.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000215\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1130.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.634\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000551\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-42.0\", \"ZT\": \"0.22\", \"formula\": \"Ba0.8Sr0.2Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.6655120556, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.029\", \"Average atomic mass (g/mol)\": \"76.52\", \"Scarcity (wt fraction/abundance)\": \"45940.0\", \"HHI (production)\": \"2579.0\", \"HHI (reserves)\": \"1839.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1820.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000317\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1740.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.77\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.00117\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-66.0\", \"ZT\": \"0.26\", \"formula\": \"Ba0.6Sr0.4Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151609, 300K\", \"marker\": \"{'radius': 0.7731340416, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.445\", \"Average atomic mass (g/mol)\": \"74.53\", \"Scarcity (wt fraction/abundance)\": \"47120.0\", \"HHI (production)\": \"2625.0\", \"HHI (reserves)\": \"1856.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"301.96\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.098\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"851.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000368\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4330.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.595\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.00351\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-118.0\", \"ZT\": \"0.28\", \"formula\": \"Ba0.4Sr0.6Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151609, 300K\", \"marker\": \"{'radius': 0.8318592116, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"1.983\", \"Average atomic mass (g/mol)\": \"72.54\", \"Scarcity (wt fraction/abundance)\": \"48360.0\", \"HHI (production)\": \"2674.0\", \"HHI (reserves)\": \"1874.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"301.96\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.098\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"285.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000396\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.245\"}, {\"doi\": \"10.1557/PROC-793-S3.3\", \"Electrical resistivity (\\u03a9cm)\": \"0.0046\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-26.0\", \"ZT\": \"0.01\", \"formula\": \"La1Ni1O3\", \"comment\": \"\", \"synthesis\": \"Evaporate nitrates (1173 K, air)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Funahashi 2003\", \"Structure\": \"ICSD #84933, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.12\", \"Scarcity (wt fraction/abundance)\": \"17470.0\", \"HHI (production)\": \"5693.0\", \"HHI (reserves)\": \"2221.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"339.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.314\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"217.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.44e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"664.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/PROC-793-S3.3\", \"Electrical resistivity (\\u03a9cm)\": \"0.00413\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-28.0\", \"ZT\": \"0.01\", \"formula\": \"La0.9Bi0.1Ni1O3\", \"comment\": \"\", \"synthesis\": \"Evaporate nitrates (1173 K, air)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Funahashi 2003\", \"Structure\": \"ICSD #84933, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"50.52\", \"Scarcity (wt fraction/abundance)\": \"4882000.0\", \"HHI (production)\": \"5452.0\", \"HHI (reserves)\": \"2483.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"339.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.314\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"242.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.96e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"810.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.2007.4569450\", \"Electrical resistivity (\\u03a9cm)\": \"0.00825\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-170.0\", \"ZT\": \"0.24\", \"formula\": \"Ca0.96Sm0.04Mn1O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sanmathi 2007\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.7339563489, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.48\", \"Scarcity (wt fraction/abundance)\": \"6638.0\", \"HHI (production)\": \"2150.0\", \"HHI (reserves)\": \"1349.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"121.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00035\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1201/9781420049718.ch22\", \"Electrical resistivity (\\u03a9cm)\": \"0.00121\", \"Seebeck coefficient (\\u03bcCV/K)\": \"199.0\", \"ZT\": \"2.29\", \"formula\": \"Ag0.15Sb0.15Te1.15Ge0.85\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Skrabek 1995\", \"Structure\": \"ICSD #2084, 300K\", \"marker\": \"{'radius': 6.8555893123, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.651\", \"Average atomic mass (g/mol)\": \"105.62\", \"Scarcity (wt fraction/abundance)\": \"605500000.0\", \"HHI (production)\": \"3762.0\", \"HHI (reserves)\": \"3810.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"479.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.973\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"824.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00326\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"39600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.853\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00843\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-335.0\", \"ZT\": \"0.93\", \"formula\": \"In0.05Co4Sb12\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 2.7884880263, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.564\", \"Average atomic mass (g/mol)\": \"106.08\", \"Scarcity (wt fraction/abundance)\": \"4312000.0\", \"HHI (production)\": \"7219.0\", \"HHI (reserves)\": \"3308.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"739.646\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.042\", \"Atoms per unit cell\": \"32.1\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"119.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00133\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"112000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.129\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00434\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-310.0\", \"ZT\": \"1.55\", \"formula\": \"In0.1Co4Sb12\", \"comment\": \"Data at 600 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 4.6502456903, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.742\", \"Average atomic mass (g/mol)\": \"106.11\", \"Scarcity (wt fraction/abundance)\": \"4314000.0\", \"HHI (production)\": \"7205.0\", \"HHI (reserves)\": \"3304.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"741.144\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.017\", \"Atoms per unit cell\": \"32.2\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"231.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00221\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"96000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.226\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00269\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-302.0\", \"ZT\": \"2.37\", \"formula\": \"In0.15Co4Sb12\", \"comment\": \"Data at 600 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 7.1024060677, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.862\", \"Average atomic mass (g/mol)\": \"106.13\", \"Scarcity (wt fraction/abundance)\": \"4316000.0\", \"HHI (production)\": \"7192.0\", \"HHI (reserves)\": \"3300.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"741.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.953\", \"Atoms per unit cell\": \"32.3\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"372.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00338\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"90900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.341\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00215\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-282.0\", \"ZT\": \"2.59\", \"formula\": \"In0.2Co4Sb12\", \"comment\": \"Data at 600 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 7.770262529, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.941\", \"Average atomic mass (g/mol)\": \"106.16\", \"Scarcity (wt fraction/abundance)\": \"4318000.0\", \"HHI (production)\": \"7180.0\", \"HHI (reserves)\": \"3295.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.742\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.924\", \"Atoms per unit cell\": \"32.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"466.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0037\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"79400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.41\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00166\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-276.0\", \"ZT\": \"3.21\", \"formula\": \"In0.25Co4Sb12\", \"comment\": \"Data at 600 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 9.6351713085, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.135\", \"Average atomic mass (g/mol)\": \"106.19\", \"Scarcity (wt fraction/abundance)\": \"4320000.0\", \"HHI (production)\": \"7167.0\", \"HHI (reserves)\": \"3291.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.89\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.858\", \"Atoms per unit cell\": \"32.5\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"604.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00459\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"76000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.483\"}, {\"doi\": \"10.1021/cm052055b\", \"Electrical resistivity (\\u03a9cm)\": \"0.00228\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-278.0\", \"ZT\": \"2.38\", \"formula\": \"In0.3Co4Sb12\", \"comment\": \"Data at 600 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"He 2006\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 7.1390221065, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.014\", \"Average atomic mass (g/mol)\": \"106.21\", \"Scarcity (wt fraction/abundance)\": \"4322000.0\", \"HHI (production)\": \"7154.0\", \"HHI (reserves)\": \"3287.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.89\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.788\", \"Atoms per unit cell\": \"32.6\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"438.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0034\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"77500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.372\"}, {\"doi\": \"10.1557/jmr.2011.163\", \"Electrical resistivity (\\u03a9cm)\": \"0.0016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-248.0\", \"ZT\": \"2.68\", \"formula\": \"In0.2Co4Sb12\", \"comment\": \"Data at 620 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Biswas 2011\", \"Structure\": \"ICSD #171715, 300K\", \"marker\": \"{'radius': 8.0520792885, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.937\", \"Average atomic mass (g/mol)\": \"106.16\", \"Scarcity (wt fraction/abundance)\": \"4318000.0\", \"HHI (production)\": \"7180.0\", \"HHI (reserves)\": \"3295.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"742.742\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.924\", \"Atoms per unit cell\": \"32.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"626.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00383\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"61300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.552\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.00171\", \"Seebeck coefficient (\\u03bcCV/K)\": \"213.0\", \"ZT\": \"1.85\", \"formula\": \"Na0.02Pb1Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 5.55635454, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.393\", \"Average atomic mass (g/mol)\": \"165.97\", \"Scarcity (wt fraction/abundance)\": \"380700000.0\", \"HHI (production)\": \"2781.0\", \"HHI (reserves)\": \"2979.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"584.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00265\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"45300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.716\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.00161\", \"Seebeck coefficient (\\u03bcCV/K)\": \"209.0\", \"ZT\": \"1.91\", \"formula\": \"Na0.02Pb1Te0.85Se0.15\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 5.715083494, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.268\", \"Average atomic mass (g/mol)\": \"162.36\", \"Scarcity (wt fraction/abundance)\": \"331500000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2827.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"623.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00272\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"43700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.839\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.00163\", \"Seebeck coefficient (\\u03bcCV/K)\": \"205.0\", \"ZT\": \"1.81\", \"formula\": \"Na0.02Pb1Te0.75Se0.25\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 5.4166740323, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.296\", \"Average atomic mass (g/mol)\": \"159.95\", \"Scarcity (wt fraction/abundance)\": \"297500000.0\", \"HHI (production)\": \"2736.0\", \"HHI (reserves)\": \"2721.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"612.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00258\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.807\"}, {\"doi\": \"10.1126/science.1159725\", \"Electrical resistivity (\\u03a9cm)\": \"0.00873\", \"Seebeck coefficient (\\u03bcCV/K)\": \"324.0\", \"ZT\": \"0.84\", \"formula\": \"Tl0.01Pb0.99Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Heremans 2008\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 2.5249879676, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.965\", \"Average atomic mass (g/mol)\": \"167.39\", \"Scarcity (wt fraction/abundance)\": \"381200000.0\", \"HHI (production)\": \"2806.0\", \"HHI (reserves)\": \"3012.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"115.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0012\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"105000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.203\"}, {\"doi\": \"10.1126/science.1159725\", \"Electrical resistivity (\\u03a9cm)\": \"0.00536\", \"Seebeck coefficient (\\u03bcCV/K)\": \"328.0\", \"ZT\": \"1.4\", \"formula\": \"Tl0.02Pb0.98Te1\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Heremans 2008\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 4.2034562118, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.01\", \"Average atomic mass (g/mol)\": \"167.37\", \"Scarcity (wt fraction/abundance)\": \"381300000.0\", \"HHI (production)\": \"2829.0\", \"HHI (reserves)\": \"3041.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"186.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.002\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"107000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.315\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00302\", \"Seebeck coefficient (\\u03bcCV/K)\": \"242.0\", \"ZT\": \"1.36\", \"formula\": \"Si0.9Ge0.1\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"700\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 4.0723311258, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.54\", \"Scarcity (wt fraction/abundance)\": \"153900.0\", \"HHI (production)\": \"4833.0\", \"HHI (reserves)\": \"1200.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"331.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"58600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00245\", \"Seebeck coefficient (\\u03bcCV/K)\": \"218.0\", \"ZT\": \"1.36\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"700\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 4.0780468215, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"407.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"47700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.00218\", \"Seebeck coefficient (\\u03bcCV/K)\": \"210.0\", \"ZT\": \"1.41\", \"formula\": \"Si0.79936Ge0.19984B0.0008\", \"comment\": \"\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 4.2323481222, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"3.817\", \"Average atomic mass (g/mol)\": \"36.98\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4927.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"458.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00202\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.205\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.00194\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-231.0\", \"ZT\": \"1.92\", \"formula\": \"Si0.7956Ge0.1989P0.0055\", \"comment\": \"\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 5.7625260444, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"3.723\", \"Average atomic mass (g/mol)\": \"36.96\", \"Scarcity (wt fraction/abundance)\": \"269600.0\", \"HHI (production)\": \"4914.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"515.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00274\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"53300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.236\"}, {\"doi\": \"10.1063/1.4765358\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-233.0\", \"ZT\": \"1.75\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"Magnetic levitation induction furnace\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Douglas 2012\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 5.2537741935, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.51\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"461.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0025\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"54300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.143\"}, {\"doi\": \"10.1063/1.1502190\", \"Electrical resistivity (\\u03a9cm)\": \"0.00277\", \"Seebeck coefficient (\\u03bcCV/K)\": \"171.0\", \"ZT\": \"0.74\", \"formula\": \"Bi2Sr2Co2O8\", \"comment\": \"\", \"synthesis\": \"Solid state reaction + extra\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Funahashi 2002\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 2.2314690578, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.068\", \"Average atomic mass (g/mol)\": \"59.93\", \"Scarcity (wt fraction/abundance)\": \"29310000.0\", \"HHI (production)\": \"4016.0\", \"HHI (reserves)\": \"4061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.53\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.59\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"362.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00106\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.299\"}, {\"doi\": \"10.1143/JJAP.39.L1127\", \"Electrical resistivity (\\u03a9cm)\": \"0.00145\", \"Seebeck coefficient (\\u03bcCV/K)\": \"173.0\", \"ZT\": \"1.46\", \"formula\": \"Ca2Co2O5\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Funahashi 2000\", \"Structure\": \"ICSD #55458, 300K\", \"marker\": \"{'radius': 4.3654737238, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.6\", \"Average atomic mass (g/mol)\": \"30.89\", \"Scarcity (wt fraction/abundance)\": \"15420.0\", \"HHI (production)\": \"2551.0\", \"HHI (reserves)\": \"1702.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"236.38\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.883\", \"Atoms per unit cell\": \"21.72\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"691.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00208\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.454\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00105\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-45.0\", \"ZT\": \"0.14\", \"formula\": \"W1O2.9\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24736, 300K\", \"marker\": \"{'radius': 0.4116779539, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.473\", \"Average atomic mass (g/mol)\": \"59.04\", \"Scarcity (wt fraction/abundance)\": \"679600.0\", \"HHI (production)\": \"5675.0\", \"HHI (reserves)\": \"3532.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1066.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.328\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"949.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000196\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2070.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.467\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.000202\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-27.0\", \"ZT\": \"0.25\", \"formula\": \"W1O2.722\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24731, 300K\", \"marker\": \"{'radius': 0.7611383118, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.88\", \"Average atomic mass (g/mol)\": \"61.09\", \"Scarcity (wt fraction/abundance)\": \"688100.0\", \"HHI (production)\": \"5740.0\", \"HHI (reserves)\": \"3570.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"883.29\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.268\", \"Atoms per unit cell\": \"72.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4960.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000362\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"731.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.231\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"120.0\", \"ZT\": \"0.06\", \"formula\": \"La1.95Sr0.05Cu1O4\", \"comment\": \"Seebeck extrapolated from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78632, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.54\", \"Scarcity (wt fraction/abundance)\": \"20920.0\", \"HHI (production)\": \"6746.0\", \"HHI (reserves)\": \"2457.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.25\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.58\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"63.1\", \"Power Factor (W/(K\\u00b2m))\": \"9.09e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00608\", \"Seebeck coefficient (\\u03bcCV/K)\": \"40.0\", \"ZT\": \"0.02\", \"formula\": \"La1.9Sr0.1Cu1O4\", \"comment\": \"Seebeck estimated Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78240, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.17\", \"Scarcity (wt fraction/abundance)\": \"20610.0\", \"HHI (production)\": \"6670.0\", \"HHI (reserves)\": \"2451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"378.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.514\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"164.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.63e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00254\", \"Seebeck coefficient (\\u03bcCV/K)\": \"2.0\", \"ZT\": \"0.000133\", \"formula\": \"La1.85Sr0.15Cu1O4\", \"comment\": \"Seebeck extrapolated from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.81\", \"Scarcity (wt fraction/abundance)\": \"20290.0\", \"HHI (production)\": \"6594.0\", \"HHI (reserves)\": \"2445.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"394.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.91e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4.84\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00136\", \"Seebeck coefficient (\\u03bcCV/K)\": \"0.0\", \"ZT\": \"5.14e-07\", \"formula\": \"La1.725Sr0.28Cu1O4\", \"comment\": \"Seebeck estimated Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.92\", \"Scarcity (wt fraction/abundance)\": \"19470.0\", \"HHI (production)\": \"6396.0\", \"HHI (reserves)\": \"2431.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"735.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.35e-10\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"0.01\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.02\", \"Seebeck coefficient (\\u03bcCV/K)\": \"295.0\", \"ZT\": \"0.3\", \"formula\": \"Tl1Cr5Se8\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Nunna 2012\", \"Structure\": \"ICSD #37123, 300K\", \"marker\": \"{'radius': 0.9137625, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"78.29\", \"Scarcity (wt fraction/abundance)\": \"11800000.0\", \"HHI (production)\": \"3230.0\", \"HHI (reserves)\": \"3274.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"581.29\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.76\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"50.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000435\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"87000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c2jm16297k\", \"Electrical resistivity (\\u03a9cm)\": \"1.691\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.00042\", \"formula\": \"Li1Mn2O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (oxalates)\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sparks 2012\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.591\", \"Power Factor (W/(K\\u00b2m))\": \"5.99e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.056\", \"Seebeck coefficient (\\u03bcCV/K)\": \"321.0\", \"ZT\": \"0.13\", \"formula\": \"Cu1Fe0.9Cr0.1O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #31918, 300K\", \"marker\": \"{'radius': 0.389506511, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.75\", \"Scarcity (wt fraction/abundance)\": \"6756.0\", \"HHI (production)\": \"1683.0\", \"HHI (reserves)\": \"1344.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"136.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.412\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"18.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000185\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"103000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.0032\", \"Seebeck coefficient (\\u03bcCV/K)\": \"146.0\", \"ZT\": \"0.46\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 1.3902227577, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"313.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000662\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.087\", \"Seebeck coefficient (\\u03bcCV/K)\": \"352.0\", \"ZT\": \"0.1\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.3003197951, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"11.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000143\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"124000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"108.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"125.0\", \"ZT\": \"1.01e-05\", \"formula\": \"W1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.96\", \"Scarcity (wt fraction/abundance)\": \"674900.0\", \"HHI (production)\": \"5639.0\", \"HHI (reserves)\": \"3511.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.00922\", \"Power Factor (W/(K\\u00b2m))\": \"1.44e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"86.0\", \"Seebeck coefficient (\\u03bcCV/K)\": \"114.0\", \"ZT\": \"1.05e-05\", \"formula\": \"W0.99O2.97Co0.02O0.03\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.65\", \"Scarcity (wt fraction/abundance)\": \"670200.0\", \"HHI (production)\": \"5615.0\", \"HHI (reserves)\": \"3500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.012\", \"Power Factor (W/(K\\u00b2m))\": \"1.5e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"20.2\", \"Seebeck coefficient (\\u03bcCV/K)\": \"120.0\", \"ZT\": \"4.99e-05\", \"formula\": \"W0.95O2.95Co0.1O0.15\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.45\", \"Scarcity (wt fraction/abundance)\": \"646800.0\", \"HHI (production)\": \"5484.0\", \"HHI (reserves)\": \"3437.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.049\", \"Power Factor (W/(K\\u00b2m))\": \"7.13e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"52.1\", \"Seebeck coefficient (\\u03bcCV/K)\": \"122.0\", \"ZT\": \"1.99e-05\", \"formula\": \"W0.9O2.7Co0.2O0.3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"54.94\", \"Scarcity (wt fraction/abundance)\": \"627100.0\", \"HHI (production)\": \"5394.0\", \"HHI (reserves)\": \"3402.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.019\", \"Power Factor (W/(K\\u00b2m))\": \"2.84e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.103\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-362.0\", \"ZT\": \"0.09\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.158\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.699\", \"Power Factor (W/(K\\u00b2m))\": \"0.000127\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"131000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00768\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-168.0\", \"ZT\": \"0.13\", \"formula\": \"Ca1Yb0.05Mn0.95O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.3825429674, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.602\", \"Average atomic mass (g/mol)\": \"29.78\", \"Scarcity (wt fraction/abundance)\": \"19730.0\", \"HHI (production)\": \"2309.0\", \"HHI (reserves)\": \"1374.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"64.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000182\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.068\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00615\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-85.0\", \"ZT\": \"0.08\", \"formula\": \"Ca1Yb0.1Mn0.9O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.614\", \"Average atomic mass (g/mol)\": \"30.96\", \"Scarcity (wt fraction/abundance)\": \"37590.0\", \"HHI (production)\": \"2722.0\", \"HHI (reserves)\": \"1465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"163.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000117\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7170.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.172\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00482\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-61.0\", \"ZT\": \"0.05\", \"formula\": \"Ca1Yb0.15Mn0.85O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.67\", \"Average atomic mass (g/mol)\": \"32.15\", \"Scarcity (wt fraction/abundance)\": \"54140.0\", \"HHI (production)\": \"3105.0\", \"HHI (reserves)\": \"1549.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"208.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.72e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3720.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.212\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-51.0\", \"ZT\": \"0.02\", \"formula\": \"Ca1Yb0.4Mn0.6O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"121500.0\", \"HHI (production)\": \"4663.0\", \"HHI (reserves)\": \"1891.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"94.2\", \"Power Factor (W/(K\\u00b2m))\": \"2.45e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-202.0\", \"ZT\": \"0.15\", \"formula\": \"In2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.4407381382, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.866\", \"Average atomic mass (g/mol)\": \"55.53\", \"Scarcity (wt fraction/abundance)\": \"4035000.0\", \"HHI (production)\": \"2843.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"51.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.00021\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.023\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00337\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-146.0\", \"ZT\": \"0.44\", \"formula\": \"In1.998Ge0.002O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 1.3309012316, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.923\", \"Average atomic mass (g/mol)\": \"55.51\", \"Scarcity (wt fraction/abundance)\": \"4032000.0\", \"HHI (production)\": \"2844.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"297.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000634\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.129\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00129\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-94.0\", \"ZT\": \"0.48\", \"formula\": \"In1.994Ge0.006O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 1.4410332085, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.584\", \"Average atomic mass (g/mol)\": \"55.48\", \"Scarcity (wt fraction/abundance)\": \"4027000.0\", \"HHI (production)\": \"2846.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"774.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000686\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8860.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.288\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00113\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.43\", \"formula\": \"In1.985Ge0.015O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 1.2881681435, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.619\", \"Average atomic mass (g/mol)\": \"55.4\", \"Scarcity (wt fraction/abundance)\": \"4016000.0\", \"HHI (production)\": \"2850.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"884.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000613\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6940.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.327\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.0014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.39\", \"formula\": \"In1.94Ge0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 1.180125422, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.9\", \"Average atomic mass (g/mol)\": \"55.02\", \"Scarcity (wt fraction/abundance)\": \"3961000.0\", \"HHI (production)\": \"2869.0\", \"HHI (reserves)\": \"1737.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"716.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000562\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7840.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.314\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00173\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-93.0\", \"ZT\": \"0.35\", \"formula\": \"In1.9Ge0.1O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 1.0545690629, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.244\", \"Average atomic mass (g/mol)\": \"54.68\", \"Scarcity (wt fraction/abundance)\": \"3910000.0\", \"HHI (production)\": \"2887.0\", \"HHI (reserves)\": \"1734.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"578.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000502\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8690.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.304\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00244\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-86.0\", \"ZT\": \"0.21\", \"formula\": \"In1.8Ge0.2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.6431930677, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"1.836\", \"Average atomic mass (g/mol)\": \"53.84\", \"Scarcity (wt fraction/abundance)\": \"3782000.0\", \"HHI (production)\": \"2932.0\", \"HHI (reserves)\": \"1727.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"410.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000306\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7460.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.382\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00136\", \"Seebeck coefficient (\\u03bcCV/K)\": \"29.0\", \"ZT\": \"0.04\", \"formula\": \"La1Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.17\", \"Scarcity (wt fraction/abundance)\": \"24200.0\", \"HHI (production)\": \"6184.0\", \"HHI (reserves)\": \"2502.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"736.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.09e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"827.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00123\", \"Seebeck coefficient (\\u03bcCV/K)\": \"32.0\", \"ZT\": \"0.06\", \"formula\": \"La0.99Sr0.01Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.06\", \"Scarcity (wt fraction/abundance)\": \"24100.0\", \"HHI (production)\": \"6158.0\", \"HHI (reserves)\": \"2500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"813.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.57e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1050.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.0011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"29.0\", \"ZT\": \"0.05\", \"formula\": \"La0.98Sr0.02Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.96\", \"Scarcity (wt fraction/abundance)\": \"24010.0\", \"HHI (production)\": \"6132.0\", \"HHI (reserves)\": \"2499.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"912.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.54e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"827.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00095\", \"Seebeck coefficient (\\u03bcCV/K)\": \"25.0\", \"ZT\": \"0.05\", \"formula\": \"La0.95Sr0.05Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247230, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.65\", \"Scarcity (wt fraction/abundance)\": \"23720.0\", \"HHI (production)\": \"6053.0\", \"HHI (reserves)\": \"2493.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.147\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1050.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.6e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"627.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000499\", \"Seebeck coefficient (\\u03bcCV/K)\": \"10.0\", \"ZT\": \"0.01\", \"formula\": \"La0.8Sr0.2Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247232, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.12\", \"Scarcity (wt fraction/abundance)\": \"22220.0\", \"HHI (production)\": \"5646.0\", \"HHI (reserves)\": \"2465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"224.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.21\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2000.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.07e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"103.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1021/cm060261t\", \"Electrical resistivity (\\u03a9cm)\": \"0.00346\", \"Seebeck coefficient (\\u03bcCV/K)\": \"117.0\", \"ZT\": \"0.28\", \"formula\": \"Yb14Mn1Sb11\", \"comment\": \"\", \"synthesis\": \"flux (Sn), Ar\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Brown 2006\", \"Structure\": \"ICSD #85638, 143K\", \"marker\": \"{'radius': 0.8335049025, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.816\", \"Average atomic mass (g/mol)\": \"146.81\", \"Scarcity (wt fraction/abundance)\": \"1966000.0\", \"HHI (production)\": \"8812.0\", \"HHI (reserves)\": \"3211.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"6058.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.129\", \"Atoms per unit cell\": \"208.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"289.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000397\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.604\"}, {\"doi\": \"10.1016/S0022-3697(96)00228-4\", \"Electrical resistivity (\\u03a9cm)\": \"0.00333\", \"Seebeck coefficient (\\u03bcCV/K)\": \"206.0\", \"ZT\": \"0.89\", \"formula\": \"Zn4Sb3\", \"comment\": \"\", \"synthesis\": \"melted, inert\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Caillat 1997\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 2.676750207, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.693\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"301.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00127\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.741\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.00325\", \"Seebeck coefficient (\\u03bcCV/K)\": \"166.0\", \"ZT\": \"0.59\", \"formula\": \"Ce1Fe2Co2Sb12\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 1.7805415385, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.69\", \"Scarcity (wt fraction/abundance)\": \"3994000.0\", \"HHI (production)\": \"7379.0\", \"HHI (reserves)\": \"3223.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"308.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000848\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.00129\", \"Seebeck coefficient (\\u03bcCV/K)\": \"176.0\", \"ZT\": \"1.68\", \"formula\": \"Ce1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 5.0426046512, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.07\", \"Average atomic mass (g/mol)\": \"107.51\", \"Scarcity (wt fraction/abundance)\": \"4000000.0\", \"HHI (production)\": \"7367.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"775.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0024\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.64\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.00107\", \"Seebeck coefficient (\\u03bcCV/K)\": \"158.0\", \"ZT\": \"1.63\", \"formula\": \"Ce1Fe3.5Co0.5Sb14\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 4.8994766355, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"2.49\", \"Average atomic mass (g/mol)\": \"108.93\", \"Scarcity (wt fraction/abundance)\": \"4120000.0\", \"HHI (production)\": \"7425.0\", \"HHI (reserves)\": \"3195.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"935.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00233\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.641\"}, {\"doi\": \"10.1109/ICT.1996.553263\", \"Electrical resistivity (\\u03a9cm)\": \"0.000886\", \"Seebeck coefficient (\\u03bcCV/K)\": \"127.0\", \"ZT\": \"1.27\", \"formula\": \"Ce1Fe4Sb12\", \"comment\": \"\", \"synthesis\": \"combination of melting and powder metallurgy techniques\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Fleurial 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 3.8229006772, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.703\", \"Average atomic mass (g/mol)\": \"107.33\", \"Scarcity (wt fraction/abundance)\": \"4005000.0\", \"HHI (production)\": \"7355.0\", \"HHI (reserves)\": \"3146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"762.5\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.426\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1130.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00182\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.132\"}, {\"doi\": \"10.1021/cm200581k\", \"Electrical resistivity (\\u03a9cm)\": \"0.033\", \"Seebeck coefficient (\\u03bcCV/K)\": \"307.0\", \"ZT\": \"0.2\", \"formula\": \"Ag1Cr1Se2\", \"comment\": \"*res and seebeck 700K and 1000K values extrapolated from 600K\", \"synthesis\": \"solid state reaction, sealed\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Gascoin 2011\", \"Structure\": \"ICSD #68423, 295K\", \"marker\": \"{'radius': 0.6011220693, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.206\", \"Average atomic mass (g/mol)\": \"79.45\", \"Scarcity (wt fraction/abundance)\": \"14290000.0\", \"HHI (production)\": \"2031.0\", \"HHI (reserves)\": \"2077.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"248.9\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.742\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"30.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000286\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"94100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.253\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-181.0\", \"ZT\": \"0.06\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.2\", \"Power Factor (W/(K\\u00b2m))\": \"7.92e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"32700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-163.0\", \"ZT\": \"0.12\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.3612280961, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"64.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000172\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-155.0\", \"ZT\": \"0.15\", \"formula\": \"Zn0.9925Al0.0075O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.4518425937, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"10740.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1618.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"90.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000215\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00796\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-147.0\", \"ZT\": \"0.19\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.5704415472, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"126.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000272\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-178.0\", \"ZT\": \"0.1\", \"formula\": \"Zn0.97Al0.03O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.11\", \"Scarcity (wt fraction/abundance)\": \"10610.0\", \"HHI (production)\": \"1360.0\", \"HHI (reserves)\": \"1608.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"45.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000143\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.034\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-58.0\", \"ZT\": \"0.0071\", \"formula\": \"Sr1Mn0.98Mo0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.28\", \"Scarcity (wt fraction/abundance)\": \"10260.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"29.8\", \"Power Factor (W/(K\\u00b2m))\": \"1.01e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.03\", \"formula\": \"Sr1Mn0.96Mo0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.44\", \"Scarcity (wt fraction/abundance)\": \"18890.0\", \"HHI (production)\": \"2515.0\", \"HHI (reserves)\": \"2089.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"57.5\", \"Power Factor (W/(K\\u00b2m))\": \"4.51e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7850.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00203\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-168.0\", \"ZT\": \"0.97\", \"formula\": \"Nb1Co1Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 2.9217355237, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"9.741\", \"Average atomic mass (g/mol)\": \"90.18\", \"Scarcity (wt fraction/abundance)\": \"221500.0\", \"HHI (production)\": \"4729.0\", \"HHI (reserves)\": \"4317.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"493.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00139\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.086\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00234\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-237.0\", \"ZT\": \"1.68\", \"formula\": \"Nb1Co1.05Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 5.0397716576, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.232\", \"Average atomic mass (g/mol)\": \"89.67\", \"Scarcity (wt fraction/abundance)\": \"219500.0\", \"HHI (production)\": \"4711.0\", \"HHI (reserves)\": \"4299.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"428.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0024\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"56100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.101\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00184\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-189.0\", \"ZT\": \"1.36\", \"formula\": \"Nb1Co1.10Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 4.0778498956, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.232\", \"Average atomic mass (g/mol)\": \"89.17\", \"Scarcity (wt fraction/abundance)\": \"217500.0\", \"HHI (production)\": \"4693.0\", \"HHI (reserves)\": \"4281.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"543.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.149\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.089\", \"Seebeck coefficient (\\u03bcCV/K)\": \"8.0\", \"ZT\": \"5.05e-05\", \"formula\": \"Ca1Mn7O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.83\", \"Scarcity (wt fraction/abundance)\": \"636.4\", \"HHI (production)\": \"1400.0\", \"HHI (reserves)\": \"1370.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"11.2\", \"Power Factor (W/(K\\u00b2m))\": \"7.21e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"64.4\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.05\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-15.0\", \"ZT\": \"0.000329\", \"formula\": \"Ca1Mn6.5Cu0.5O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.05\", \"Scarcity (wt fraction/abundance)\": \"1387.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1359.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"20.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.7e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"235.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.033\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-27.0\", \"ZT\": \"0.0016\", \"formula\": \"Ca1Mn6Cu1O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.26\", \"Scarcity (wt fraction/abundance)\": \"2126.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1348.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"30.6\", \"Power Factor (W/(K\\u00b2m))\": \"2.29e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"747.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"1.167\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-30.0\", \"ZT\": \"5.46e-05\", \"formula\": \"Li1Mn2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.857\", \"Power Factor (W/(K\\u00b2m))\": \"7.8e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"911.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-23.0\", \"ZT\": \"0.00239\", \"formula\": \"Pr0.5Ca0.5Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #85650, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.69\", \"Scarcity (wt fraction/abundance)\": \"40990.0\", \"HHI (production)\": \"4428.0\", \"HHI (reserves)\": \"1928.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"221.92\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.096\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"62.1\", \"Power Factor (W/(K\\u00b2m))\": \"3.41e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"549.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000715\", \"Seebeck coefficient (\\u03bcCV/K)\": \"17.0\", \"ZT\": \"0.03\", \"formula\": \"Mo3Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"4.452\", \"Average atomic mass (g/mol)\": \"114.04\", \"Scarcity (wt fraction/abundance)\": \"639700000.0\", \"HHI (production)\": \"2718.0\", \"HHI (reserves)\": \"5052.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1400.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.84e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"274.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.537\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000817\", \"Seebeck coefficient (\\u03bcCV/K)\": \"14.0\", \"ZT\": \"0.02\", \"formula\": \"Mo6Te7S1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.978\", \"Average atomic mass (g/mol)\": \"107.22\", \"Scarcity (wt fraction/abundance)\": \"595400000.0\", \"HHI (production)\": \"2661.0\", \"HHI (reserves)\": \"4975.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1220.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.39e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"195.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.525\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000946\", \"Seebeck coefficient (\\u03bcCV/K)\": \"12.0\", \"ZT\": \"0.01\", \"formula\": \"Mo6Te6S2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.931\", \"Average atomic mass (g/mol)\": \"100.39\", \"Scarcity (wt fraction/abundance)\": \"545100000.0\", \"HHI (production)\": \"2596.0\", \"HHI (reserves)\": \"4888.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1060.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.44e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"137.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.616\"}, {\"doi\": \"10.1109/ICT.2006.331289\", \"Electrical resistivity (\\u03a9cm)\": \"0.00392\", \"Seebeck coefficient (\\u03bcCV/K)\": \"203.0\", \"ZT\": \"0.74\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kuriyama 2006\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 2.2076547436, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"10.01\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"255.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00105\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"41200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.044\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00865\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-110.0\", \"ZT\": \"0.1\", \"formula\": \"Sr2Ti0.8Nb0.2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.48\", \"Average atomic mass (g/mol)\": \"42.3\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3261.0\", \"HHI (reserves)\": \"2636.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"187.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.357\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"116.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000141\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.08\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00429\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-98.0\", \"ZT\": \"0.16\", \"formula\": \"Sr3Ti1.6Nb0.4O7\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.4728052077, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.72\", \"Average atomic mass (g/mol)\": \"40.72\", \"Scarcity (wt fraction/abundance)\": \"5611.0\", \"HHI (production)\": \"3187.0\", \"HHI (reserves)\": \"2641.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"305.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.708\", \"Atoms per unit cell\": \"24.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"233.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000225\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9660.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.146\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00171\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-110.0\", \"ZT\": \"0.5\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162889, 15K\", \"marker\": \"{'radius': 1.486485, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.92\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"240.63\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.032\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"585.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000708\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.203\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00918\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-251.0\", \"ZT\": \"0.48\", \"formula\": \"Sr0.95La0.05Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 1.4417224441, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.21\", \"Scarcity (wt fraction/abundance)\": \"2291.0\", \"HHI (production)\": \"2640.0\", \"HHI (reserves)\": \"1987.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"109.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000687\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"63000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00366\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-179.0\", \"ZT\": \"0.61\", \"formula\": \"Sr0.9La0.1Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 1.8389560274, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.83\", \"Average atomic mass (g/mol)\": \"37.72\", \"Scarcity (wt fraction/abundance)\": \"3205.0\", \"HHI (production)\": \"2856.0\", \"HHI (reserves)\": \"2006.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"273.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000876\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"32000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.122\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00119\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-113.0\", \"ZT\": \"0.75\", \"formula\": \"Sr0.8La0.2Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65094, 300K\", \"marker\": \"{'radius': 2.2494590572, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.75\", \"Scarcity (wt fraction/abundance)\": \"4961.0\", \"HHI (production)\": \"3271.0\", \"HHI (reserves)\": \"2041.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.0\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"839.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00107\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00276\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-255.0\", \"ZT\": \"1.65\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 4.9479358135, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"4.552\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"362.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00236\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"65100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.136\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00128\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-211.0\", \"ZT\": \"2.45\", \"formula\": \"Ti0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 7.3506259372, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"4.818\", \"Average atomic mass (g/mol)\": \"75.24\", \"Scarcity (wt fraction/abundance)\": \"236100.0\", \"HHI (production)\": \"1890.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"784.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0035\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.278\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000908\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-189.0\", \"ZT\": \"2.74\", \"formula\": \"Ti0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 8.2230419875, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.085\", \"Average atomic mass (g/mol)\": \"75.39\", \"Scarcity (wt fraction/abundance)\": \"235900.0\", \"HHI (production)\": \"1918.0\", \"HHI (reserves)\": \"1638.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1100.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00392\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.37\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000567\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-146.0\", \"ZT\": \"2.64\", \"formula\": \"Ti0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 7.9075505463, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.252\", \"Average atomic mass (g/mol)\": \"75.84\", \"Scarcity (wt fraction/abundance)\": \"235200.0\", \"HHI (production)\": \"2004.0\", \"HHI (reserves)\": \"1726.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1760.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00377\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.574\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.0028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-285.0\", \"ZT\": \"2.03\", \"formula\": \"Zr1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 6.0835388107, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.985\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"200100.0\", \"HHI (production)\": \"2519.0\", \"HHI (reserves)\": \"1929.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"357.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0029\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"81000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.102\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00135\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-228.0\", \"ZT\": \"2.71\", \"formula\": \"Zr0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 8.1256977864, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.052\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200200.0\", \"HHI (production)\": \"2537.0\", \"HHI (reserves)\": \"1950.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"741.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00387\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"52200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.209\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000874\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-194.0\", \"ZT\": \"3.0\", \"formula\": \"Zr0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 9.0137739473, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.452\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200400.0\", \"HHI (production)\": \"2554.0\", \"HHI (reserves)\": \"1972.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1140.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00429\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"37500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.303\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000474\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-129.0\", \"ZT\": \"2.47\", \"formula\": \"Zr0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 7.4121079239, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.668\", \"Average atomic mass (g/mol)\": \"89.57\", \"Scarcity (wt fraction/abundance)\": \"200900.0\", \"HHI (production)\": \"2608.0\", \"HHI (reserves)\": \"2036.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2110.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00353\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.541\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.029\", \"Seebeck coefficient (\\u03bcCV/K)\": \"84.0\", \"ZT\": \"0.02\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"34.8\", \"Power Factor (W/(K\\u00b2m))\": \"2.47e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.025\", \"Seebeck coefficient (\\u03bcCV/K)\": \"89.0\", \"ZT\": \"0.02\", \"formula\": \"La0.05Ca2.85Co3.8O8.55\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.6\", \"Scarcity (wt fraction/abundance)\": \"17300.0\", \"HHI (production)\": \"2612.0\", \"HHI (reserves)\": \"1776.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"39.8\", \"Power Factor (W/(K\\u00b2m))\": \"3.12e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7850.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.021\", \"Seebeck coefficient (\\u03bcCV/K)\": \"92.0\", \"ZT\": \"0.03\", \"formula\": \"La0.3Ca2.7Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"33.1\", \"Scarcity (wt fraction/abundance)\": \"18350.0\", \"HHI (production)\": \"3029.0\", \"HHI (reserves)\": \"1870.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"48.3\", \"Power Factor (W/(K\\u00b2m))\": \"4.13e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8540.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.023\", \"Seebeck coefficient (\\u03bcCV/K)\": \"95.0\", \"ZT\": \"0.03\", \"formula\": \"La0.45Ca2.55Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"34.03\", \"Scarcity (wt fraction/abundance)\": \"18900.0\", \"HHI (production)\": \"3266.0\", \"HHI (reserves)\": \"1923.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"43.5\", \"Power Factor (W/(K\\u00b2m))\": \"3.94e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9040.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000693\", \"Seebeck coefficient (\\u03bcCV/K)\": \"51.0\", \"ZT\": \"0.26\", \"formula\": \"Cr1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #40697, 300K\", \"marker\": \"{'radius': 0.7946880129, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.69\", \"Average atomic mass (g/mol)\": \"58.82\", \"Scarcity (wt fraction/abundance)\": \"557400.0\", \"HHI (production)\": \"1985.0\", \"HHI (reserves)\": \"3955.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.41\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.608\", \"Atoms per unit cell\": \"15.3\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1440.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000378\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.916\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000878\", \"Seebeck coefficient (\\u03bcCV/K)\": \"48.0\", \"ZT\": \"0.18\", \"formula\": \"Mn1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #249898, 300K\", \"marker\": \"{'radius': 0.5437411727, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.353\", \"Average atomic mass (g/mol)\": \"59.07\", \"Scarcity (wt fraction/abundance)\": \"554800.0\", \"HHI (production)\": \"1871.0\", \"HHI (reserves)\": \"3777.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"816.76\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.15\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1140.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000259\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2270.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.827\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.00076\", \"Seebeck coefficient (\\u03bcCV/K)\": \"45.0\", \"ZT\": \"0.19\", \"formula\": \"Fe1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #632653, 300K\", \"marker\": \"{'radius': 0.566125655, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.775\", \"Average atomic mass (g/mol)\": \"59.14\", \"Scarcity (wt fraction/abundance)\": \"554000.0\", \"HHI (production)\": \"1937.0\", \"HHI (reserves)\": \"3740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"807.22\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.938\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1320.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00027\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2050.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.81\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000457\", \"Seebeck coefficient (\\u03bcCV/K)\": \"21.0\", \"ZT\": \"0.07\", \"formula\": \"Ni2.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602930, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"4.237\", \"Average atomic mass (g/mol)\": \"59.35\", \"Scarcity (wt fraction/abundance)\": \"528800.0\", \"HHI (production)\": \"1782.0\", \"HHI (reserves)\": \"3642.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"801.34\", \"Average atomic volume (\\u212b\\u00b3)\": \"16.695\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2190.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.49e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"434.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.883\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.00169\", \"Seebeck coefficient (\\u03bcCV/K)\": \"105.0\", \"ZT\": \"0.46\", \"formula\": \"Cu4.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602374, 300K\", \"marker\": \"{'radius': 1.3790666643, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.791\", \"Average atomic mass (g/mol)\": \"60.36\", \"Scarcity (wt fraction/abundance)\": \"465000.0\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"3380.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"853.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.807\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"592.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000657\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.565\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.005\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-120.0\", \"ZT\": \"0.2\", \"formula\": \"Ca0.9Bi0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #98592, 300K\", \"marker\": \"{'radius': 0.6022112758, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.214\", \"Average atomic mass (g/mol)\": \"31.98\", \"Scarcity (wt fraction/abundance)\": \"7688000.0\", \"HHI (production)\": \"2260.0\", \"HHI (reserves)\": \"1887.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.57\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.678\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000287\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.154\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00666\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-60.0\", \"ZT\": \"0.04\", \"formula\": \"Ca0.9Ce0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.6\", \"Scarcity (wt fraction/abundance)\": \"1819.0\", \"HHI (production)\": \"2506.0\", \"HHI (reserves)\": \"1440.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"150.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.4e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-103.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"63.1\", \"Power Factor (W/(K\\u00b2m))\": \"6.64e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00788\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-147.0\", \"ZT\": \"0.19\", \"formula\": \"Ca0.9Sm0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.5739442783, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.81\", \"Scarcity (wt fraction/abundance)\": \"15330.0\", \"HHI (production)\": \"2553.0\", \"HHI (reserves)\": \"1451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"127.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000273\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.067\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-81.0\", \"ZT\": \"0.00686\", \"formula\": \"Ca0.9Sb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.24\", \"Scarcity (wt fraction/abundance)\": \"403100.0\", \"HHI (production)\": \"2295.0\", \"HHI (reserves)\": \"1442.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"14.9\", \"Power Factor (W/(K\\u00b2m))\": \"9.8e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6570.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00855\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-117.0\", \"ZT\": \"0.11\", \"formula\": \"Ca0.9La0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.3358789774, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.58\", \"Scarcity (wt fraction/abundance)\": \"2861.0\", \"HHI (production)\": \"2501.0\", \"HHI (reserves)\": \"1438.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"117.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00016\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.061\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-277.0\", \"ZT\": \"0.09\", \"formula\": \"Ca0.9Pb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.95\", \"Scarcity (wt fraction/abundance)\": \"11170.0\", \"HHI (production)\": \"1922.0\", \"HHI (reserves)\": \"1336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"16.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000127\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"76800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.231\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-411.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.9In0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.1\", \"Scarcity (wt fraction/abundance)\": \"372600.0\", \"HHI (production)\": \"1921.0\", \"HHI (reserves)\": \"1325.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.333\", \"Power Factor (W/(K\\u00b2m))\": \"7.32e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"169000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"2.082\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-255.0\", \"ZT\": \"0.00219\", \"formula\": \"Ca0.9Sn0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"35350.0\", \"HHI (production)\": \"1866.0\", \"HHI (reserves)\": \"1298.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.48\", \"Power Factor (W/(K\\u00b2m))\": \"3.13e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"65100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.485\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-332.0\", \"ZT\": \"0.02\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.311\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.061\", \"Power Factor (W/(K\\u00b2m))\": \"2.27e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"110000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00106\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"3.408\", \"Seebeck coefficient (\\u03bcCV/K)\": \"634.0\", \"ZT\": \"0.00825\", \"formula\": \"Cu1Cr1O2\", \"comment\": \"*res data at 300K/400K extrapolated from 600K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157800, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.884\", \"Average atomic mass (g/mol)\": \"36.88\", \"Scarcity (wt fraction/abundance)\": \"8516.0\", \"HHI (production)\": \"1881.0\", \"HHI (reserves)\": \"2193.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.293\", \"Power Factor (W/(K\\u00b2m))\": \"1.18e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"402000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000103\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.472\", \"Seebeck coefficient (\\u03bcCV/K)\": \"428.0\", \"ZT\": \"0.03\", \"formula\": \"Cu1Cr0.99Mg0.01O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157801, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.704\", \"Average atomic mass (g/mol)\": \"36.82\", \"Scarcity (wt fraction/abundance)\": \"8514.0\", \"HHI (production)\": \"1882.0\", \"HHI (reserves)\": \"2184.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.118\", \"Power Factor (W/(K\\u00b2m))\": \"3.88e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"183000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000634\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.265\", \"Seebeck coefficient (\\u03bcCV/K)\": \"368.0\", \"ZT\": \"0.04\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.838\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.772\", \"Power Factor (W/(K\\u00b2m))\": \"5.11e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"135000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0011\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.049\", \"Seebeck coefficient (\\u03bcCV/K)\": \"290.0\", \"ZT\": \"0.12\", \"formula\": \"Cu1Cr0.97Mg0.03O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157803, 300K\", \"marker\": \"{'radius': 0.3629059556, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.666\", \"Average atomic mass (g/mol)\": \"36.68\", \"Scarcity (wt fraction/abundance)\": \"8511.0\", \"HHI (production)\": \"1885.0\", \"HHI (reserves)\": \"2165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.928\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"20.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000173\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"83900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00621\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.047\", \"Seebeck coefficient (\\u03bcCV/K)\": \"270.0\", \"ZT\": \"0.11\", \"formula\": \"Cu1Cr0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157804, 300K\", \"marker\": \"{'radius': 0.3270337025, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"7.973\", \"Average atomic mass (g/mol)\": \"36.61\", \"Scarcity (wt fraction/abundance)\": \"8509.0\", \"HHI (production)\": \"1886.0\", \"HHI (reserves)\": \"2156.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.933\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000156\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"73000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00457\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"282.0\", \"ZT\": \"0.14\", \"formula\": \"Cu1Cr0.95Mg0.05O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157805, 300K\", \"marker\": \"{'radius': 0.4095259036, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"8.087\", \"Average atomic mass (g/mol)\": \"36.54\", \"Scarcity (wt fraction/abundance)\": \"8507.0\", \"HHI (production)\": \"1887.0\", \"HHI (reserves)\": \"2146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.16\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.93\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000195\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"79300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00519\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.000484\", \"Seebeck coefficient (\\u03bcCV/K)\": \"146.0\", \"ZT\": \"3.08\", \"formula\": \"Na1Co2O4\", \"comment\": \"\", \"synthesis\": \"flux (NaCl), air\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 9.2429485856, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"5.702\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2060.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0044\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.618\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.0034\", \"Seebeck coefficient (\\u03bcCV/K)\": \"161.0\", \"ZT\": \"0.53\", \"formula\": \"Na1Co2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 1.6010029412, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.093\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"294.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000762\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.24\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.085\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-160.0\", \"ZT\": \"0.02\", \"formula\": \"Zn1O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.69\", \"Scarcity (wt fraction/abundance)\": \"10780.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1621.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"11.8\", \"Power Factor (W/(K\\u00b2m))\": \"3.01e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.068\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-134.0\", \"ZT\": \"0.02\", \"formula\": \"Zn0.98Al0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.31\", \"Scarcity (wt fraction/abundance)\": \"10670.0\", \"HHI (production)\": \"1361.0\", \"HHI (reserves)\": \"1612.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"14.7\", \"Power Factor (W/(K\\u00b2m))\": \"2.62e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.05\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-125.0\", \"ZT\": \"0.02\", \"formula\": \"Zn0.97Al0.03O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.11\", \"Scarcity (wt fraction/abundance)\": \"10610.0\", \"HHI (production)\": \"1360.0\", \"HHI (reserves)\": \"1608.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"20.1\", \"Power Factor (W/(K\\u00b2m))\": \"3.14e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.047\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-113.0\", \"ZT\": \"0.02\", \"formula\": \"Zn0.95Al0.05O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"39.73\", \"Scarcity (wt fraction/abundance)\": \"10490.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1599.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.4\", \"Power Factor (W/(K\\u00b2m))\": \"2.71e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.034\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-171.0\", \"ZT\": \"0.06\", \"formula\": \"Zn0.97Al0.025Ti0.005O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.17\", \"Scarcity (wt fraction/abundance)\": \"10600.0\", \"HHI (production)\": \"1359.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"29.6\", \"Power Factor (W/(K\\u00b2m))\": \"8.62e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.029\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-148.0\", \"ZT\": \"0.05\", \"formula\": \"Zn0.97Al0.02Ti0.01O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.22\", \"Scarcity (wt fraction/abundance)\": \"10580.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"34.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.45e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-143.0\", \"ZT\": \"0.06\", \"formula\": \"Zn0.97Al0.015Ti0.015O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.27\", \"Scarcity (wt fraction/abundance)\": \"10570.0\", \"HHI (production)\": \"1357.0\", \"HHI (reserves)\": \"1610.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"38.5\", \"Power Factor (W/(K\\u00b2m))\": \"7.88e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.024\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-139.0\", \"ZT\": \"0.06\", \"formula\": \"Zn0.97Al0.01Ti0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.32\", \"Scarcity (wt fraction/abundance)\": \"10560.0\", \"HHI (production)\": \"1356.0\", \"HHI (reserves)\": \"1611.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"42.5\", \"Power Factor (W/(K\\u00b2m))\": \"8.22e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-236.0\", \"ZT\": \"1.8\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 5.4010810405, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.274\", \"Average atomic mass (g/mol)\": \"104.09\", \"Scarcity (wt fraction/abundance)\": \"262000.0\", \"HHI (production)\": \"2643.0\", \"HHI (reserves)\": \"2022.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"462.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00257\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"55700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.241\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00177\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-277.0\", \"ZT\": \"3.03\", \"formula\": \"Zr0.4Hf0.4Ti0.2Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 9.1003371229, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.196\", \"Average atomic mass (g/mol)\": \"98.29\", \"Scarcity (wt fraction/abundance)\": \"258100.0\", \"HHI (production)\": \"2524.0\", \"HHI (reserves)\": \"1954.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"566.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00433\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"76600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.303\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00228\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-348.0\", \"ZT\": \"3.72\", \"formula\": \"Zr0.35Hf0.35Ti0.3Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 11.1526667972, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.942\", \"Average atomic mass (g/mol)\": \"95.39\", \"Scarcity (wt fraction/abundance)\": \"256000.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"438.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00531\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"121000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.255\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00163\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-328.0\", \"ZT\": \"4.62\", \"formula\": \"Zr0.25Hf0.25Ti0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 13.8539439224, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.254\", \"Average atomic mass (g/mol)\": \"89.59\", \"Scarcity (wt fraction/abundance)\": \"251300.0\", \"HHI (production)\": \"2315.0\", \"HHI (reserves)\": \"1836.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"612.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0066\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"108000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.321\"}, {\"doi\": \"10.1063/1.1868063\", \"Electrical resistivity (\\u03a9cm)\": \"0.00148\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-261.0\", \"ZT\": \"3.21\", \"formula\": \"Zr0.15Hf0.15Ti0.7Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sakurada 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 9.6260618027, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.157\", \"Average atomic mass (g/mol)\": \"83.79\", \"Scarcity (wt fraction/abundance)\": \"246000.0\", \"HHI (production)\": \"2152.0\", \"HHI (reserves)\": \"1744.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"675.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00458\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"67900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.365\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.0013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"129.0\", \"ZT\": \"0.89\", \"formula\": \"Ce1Fe4Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #621065, 300K\", \"marker\": \"{'radius': 2.6774426195, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.33\", \"Scarcity (wt fraction/abundance)\": \"4005000.0\", \"HHI (production)\": \"7355.0\", \"HHI (reserves)\": \"3146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"762.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.421\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"768.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00127\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00202\", \"Seebeck coefficient (\\u03bcCV/K)\": \"150.0\", \"ZT\": \"0.78\", \"formula\": \"Ce1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 2.3414379243, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.51\", \"Scarcity (wt fraction/abundance)\": \"4000000.0\", \"HHI (production)\": \"7367.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"496.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00111\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00331\", \"Seebeck coefficient (\\u03bcCV/K)\": \"162.0\", \"ZT\": \"0.56\", \"formula\": \"Ce1Fe2.5Co1.5Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 1.665819108, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.6\", \"Scarcity (wt fraction/abundance)\": \"3997000.0\", \"HHI (production)\": \"7373.0\", \"HHI (reserves)\": \"3204.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"302.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000793\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00488\", \"Seebeck coefficient (\\u03bcCV/K)\": \"164.0\", \"ZT\": \"0.39\", \"formula\": \"Ce1Fe2Co2Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 1.1569712375, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.69\", \"Scarcity (wt fraction/abundance)\": \"3994000.0\", \"HHI (production)\": \"7379.0\", \"HHI (reserves)\": \"3223.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"205.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000551\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00609\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-141.0\", \"ZT\": \"0.23\", \"formula\": \"Ce1Fe1Co3Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.6842872543, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.88\", \"Scarcity (wt fraction/abundance)\": \"3988000.0\", \"HHI (production)\": \"7391.0\", \"HHI (reserves)\": \"3261.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"164.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000326\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-36.0\", \"ZT\": \"0.00742\", \"formula\": \"Ce1Fe1.5Co2.5Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.78\", \"Scarcity (wt fraction/abundance)\": \"3991000.0\", \"HHI (production)\": \"7385.0\", \"HHI (reserves)\": \"3242.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"83.8\", \"Power Factor (W/(K\\u00b2m))\": \"1.06e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1260.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00232\", \"Seebeck coefficient (\\u03bcCV/K)\": \"210.0\", \"ZT\": \"1.34\", \"formula\": \"La1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #280118, 295K\", \"marker\": \"{'radius': 4.0141247056, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"1.57\", \"Average atomic mass (g/mol)\": \"107.44\", \"Scarcity (wt fraction/abundance)\": \"4003000.0\", \"HHI (production)\": \"7366.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"752.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.143\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"431.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00191\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.469\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00236\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-238.0\", \"ZT\": \"1.68\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 5.0338777305, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"3.113\", \"Average atomic mass (g/mol)\": \"104.09\", \"Scarcity (wt fraction/abundance)\": \"262000.0\", \"HHI (production)\": \"2643.0\", \"HHI (reserves)\": \"2022.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"423.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0024\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"56600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.232\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00154\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-307.0\", \"ZT\": \"4.27\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1.998Sb0.002\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 12.8188406736, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.947\", \"Average atomic mass (g/mol)\": \"107.74\", \"Scarcity (wt fraction/abundance)\": \"314900.0\", \"HHI (production)\": \"2632.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"648.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0061\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"94200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.375\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00132\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-274.0\", \"ZT\": \"3.99\", \"formula\": \"Zr0.5Hf0.5Ni1Sn1.994Sb0.006\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 11.9565903231, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"2.964\", \"Average atomic mass (g/mol)\": \"107.75\", \"Scarcity (wt fraction/abundance)\": \"320000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"1919.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"758.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00569\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"75100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.437\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00215\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-287.0\", \"ZT\": \"2.69\", \"formula\": \"Zr0.4Hf0.4Ti0.2Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 8.0553013668, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"98.29\", \"Scarcity (wt fraction/abundance)\": \"258100.0\", \"HHI (production)\": \"2524.0\", \"HHI (reserves)\": \"1954.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"465.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00384\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"82500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00235\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-345.0\", \"ZT\": \"3.55\", \"formula\": \"Zr0.35Hf0.35Ti0.3Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 10.6575974401, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"95.39\", \"Scarcity (wt fraction/abundance)\": \"256000.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1917.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"426.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00508\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"119000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00203\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-358.0\", \"ZT\": \"4.41\", \"formula\": \"Zr0.3Hf0.3Ti0.4Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 13.2407715619, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"92.49\", \"Scarcity (wt fraction/abundance)\": \"253700.0\", \"HHI (production)\": \"2389.0\", \"HHI (reserves)\": \"1878.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"492.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00631\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"128000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00189\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-334.0\", \"ZT\": \"4.13\", \"formula\": \"Zr0.25Hf0.25Ti0.5Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 12.3978403355, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"89.59\", \"Scarcity (wt fraction/abundance)\": \"251300.0\", \"HHI (production)\": \"2315.0\", \"HHI (reserves)\": \"1836.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"530.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0059\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"111000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2004.05.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.00168\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-261.0\", \"ZT\": \"2.83\", \"formula\": \"Zr0.15Hf0.15Ti0.7Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Shutoh 2005\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 8.4858728826, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"83.79\", \"Scarcity (wt fraction/abundance)\": \"246000.0\", \"HHI (production)\": \"2152.0\", \"HHI (reserves)\": \"1744.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"594.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00404\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"68100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://orbit.dtu.dk/en/publications/improvement-of-niobium-doped-srtio3-by-nanostructuring(2b6f4b33-1a6f-4472-ac18-6996f91cd743).html\", \"Electrical resistivity (\\u03a9cm)\": \"0.00461\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-122.0\", \"ZT\": \"0.23\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Sonne 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.6808109556, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"6.14\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"217.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000324\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.06\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00459\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-147.0\", \"ZT\": \"0.33\", \"formula\": \"Sr1Dy0.08Ti0.92O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.98926002, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.17\", \"Average atomic mass (g/mol)\": \"38.53\", \"Scarcity (wt fraction/abundance)\": \"13120.0\", \"HHI (production)\": \"2920.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"218.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000471\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.117\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00227\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-96.0\", \"ZT\": \"0.28\", \"formula\": \"Sr1Nd0.17Ti0.83O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.852719616, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.87\", \"Average atomic mass (g/mol)\": \"39.97\", \"Scarcity (wt fraction/abundance)\": \"4528.0\", \"HHI (production)\": \"3337.0\", \"HHI (reserves)\": \"2128.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"441.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000406\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9220.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.194\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00195\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-94.0\", \"ZT\": \"0.32\", \"formula\": \"Sr1Nd0.2Ti0.8O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9581494272, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.45\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3484.0\", \"HHI (reserves)\": \"2153.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"512.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000456\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8910.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.253\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00186\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-81.0\", \"ZT\": \"0.24\", \"formula\": \"Sr1Nd0.24Ti0.76O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.7344134973, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.76\", \"Average atomic mass (g/mol)\": \"41.32\", \"Scarcity (wt fraction/abundance)\": \"5689.0\", \"HHI (production)\": \"3673.0\", \"HHI (reserves)\": \"2186.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"537.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00035\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6510.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.244\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00335\", \"Seebeck coefficient (\\u03bcCV/K)\": \"185.0\", \"ZT\": \"0.71\", \"formula\": \"Zn4Sb3\", \"comment\": \"*extrapolated from 600K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 2.1374326602, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.74\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"298.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00102\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.688\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00317\", \"Seebeck coefficient (\\u03bcCV/K)\": \"188.0\", \"ZT\": \"0.78\", \"formula\": \"Zn4Sb3\", \"comment\": \"*extrapolated from 600K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 2.3535936289, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.743\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"316.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00112\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.726\"}, {\"doi\": \"10.1039/c0jm02011g\", \"Electrical resistivity (\\u03a9cm)\": \"0.00329\", \"Seebeck coefficient (\\u03bcCV/K)\": \"192.0\", \"ZT\": \"0.78\", \"formula\": \"Zn4Sb3\", \"comment\": \"*extrapolated from 600K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #52403, 300K\", \"marker\": \"{'radius': 2.3491264868, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.75\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"2919000.0\", \"HHI (production)\": \"5264.0\", \"HHI (reserves)\": \"2783.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1610.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"25.566\", \"Atoms per unit cell\": \"63.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"304.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00112\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.692\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"1.786\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-330.0\", \"ZT\": \"0.00426\", \"formula\": \"Zn1O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"14.65\", \"Average atomic mass (g/mol)\": \"40.69\", \"Scarcity (wt fraction/abundance)\": \"10780.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1621.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.345\", \"Power Factor (W/(K\\u00b2m))\": \"6.09e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"109000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00109\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00912\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-166.0\", \"ZT\": \"0.21\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.6353238574, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"13.525\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"94.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.000303\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.012\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00398\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-182.0\", \"ZT\": \"0.58\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.7514857675, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"13.525\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000834\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"33200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.025\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00148\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-171.0\", \"ZT\": \"1.39\", \"formula\": \"Zn0.98Al0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 4.1749016052, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"12.4\", \"Average atomic mass (g/mol)\": \"40.31\", \"Scarcity (wt fraction/abundance)\": \"10670.0\", \"HHI (production)\": \"1361.0\", \"HHI (reserves)\": \"1612.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"548.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00199\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.075\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00209\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-196.0\", \"ZT\": \"1.28\", \"formula\": \"Zn0.95Al0.05O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 3.8473459639, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"14.3\", \"Average atomic mass (g/mol)\": \"39.73\", \"Scarcity (wt fraction/abundance)\": \"10490.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1599.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"450.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00183\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.054\"}, {\"doi\": \"10.1016/j.jallcom.2010.06.195\", \"Electrical resistivity (\\u03a9cm)\": \"0.055\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-100.0\", \"ZT\": \"0.01\", \"formula\": \"Sr1Nb0.15Ti0.85O3\", \"comment\": \"*Values at 1000K extrapolated from 900K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Wang 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.49\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"5257.0\", \"HHI (production)\": \"2915.0\", \"HHI (reserves)\": \"2484.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"18.1\", \"Power Factor (W/(K\\u00b2m))\": \"1.81e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00887\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.00123\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-102.0\", \"ZT\": \"0.6\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"Czochralski method, He\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 1.7857090317, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.62\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"813.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00085\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.857\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.00161\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-107.0\", \"ZT\": \"0.5\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 1.5039736174, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.3\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"621.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000716\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.816\"}, {\"doi\": \"10.1063/1.2163979\", \"Electrical resistivity (\\u03a9cm)\": \"0.00142\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-150.0\", \"ZT\": \"1.11\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"Czochralski method, argon\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Saramat 2006\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 3.332157969, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.56\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"705.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00159\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.772\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.000948\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-89.0\", \"ZT\": \"0.59\", \"formula\": \"Bi1.2S1.2Ti2S4\", \"comment\": \"\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 1.7593867342, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.11\", \"Average atomic mass (g/mol)\": \"61.1\", \"Scarcity (wt fraction/abundance)\": \"28740000.0\", \"HHI (production)\": \"3036.0\", \"HHI (reserves)\": \"3543.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1050.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000838\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7940.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.854\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-129.0\", \"ZT\": \"0.53\", \"formula\": \"Pb1.8S1.8Ti2S4\", \"comment\": \"\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 1.6049650874, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.95\", \"Average atomic mass (g/mol)\": \"68.19\", \"Scarcity (wt fraction/abundance)\": \"48160.0\", \"HHI (production)\": \"1920.0\", \"HHI (reserves)\": \"1526.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"460.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000764\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.403\"}, {\"doi\": \"10.3390/ma3042606\", \"Electrical resistivity (\\u03a9cm)\": \"0.00217\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-141.0\", \"ZT\": \"0.64\", \"formula\": \"Sn1.2S1.2Ti2S4\", \"comment\": \"\", \"synthesis\": \"solid-liquid-vapor reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Wan 2010\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 1.9149836247, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.69\", \"Average atomic mass (g/mol)\": \"48.21\", \"Scarcity (wt fraction/abundance)\": \"157400.0\", \"HHI (production)\": \"1480.0\", \"HHI (reserves)\": \"1355.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"175.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.857\", \"Atoms per unit cell\": \"8.4\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"460.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000912\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.465\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.00287\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-98.0\", \"ZT\": \"0.24\", \"formula\": \"Ba8Au5.14Si39.51\", \"comment\": \"*extrapolated from 676 K\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"700\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 0.7063216463, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.45\", \"Average atomic mass (g/mol)\": \"61.17\", \"Scarcity (wt fraction/abundance)\": \"78590000.0\", \"HHI (production)\": \"2988.0\", \"HHI (reserves)\": \"1472.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"348.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000336\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9650.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.243\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.00275\", \"Seebeck coefficient (\\u03bcCV/K)\": \"136.0\", \"ZT\": \"0.47\", \"formula\": \"Ba8Au5.59Si39.01\", \"comment\": \"*extrapolated from 676 K\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"700\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 1.4224094487, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.41\", \"Average atomic mass (g/mol)\": \"62.65\", \"Scarcity (wt fraction/abundance)\": \"83530000.0\", \"HHI (production)\": \"2930.0\", \"HHI (reserves)\": \"1462.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"364.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000677\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.258\"}, {\"doi\": \"10.1063/1.3682585\", \"Electrical resistivity (\\u03a9cm)\": \"0.000789\", \"Seebeck coefficient (\\u03bcCV/K)\": \"77.0\", \"ZT\": \"0.52\", \"formula\": \"Ba8Au6.10Si38.97\", \"comment\": \"*extrapolated from 676 K\", \"synthesis\": \"melted, inert\", \"form\": \"polyrystalline\", \"temperature\": \"700\", \"author\": \"Candolfi 2012\", \"Structure\": \"ICSD #40567, 300K\", \"marker\": \"{'radius': 1.5727368175, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.95\", \"Average atomic mass (g/mol)\": \"63.97\", \"Scarcity (wt fraction/abundance)\": \"88490000.0\", \"HHI (production)\": \"2876.0\", \"HHI (reserves)\": \"1450.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1132.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"20.963\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1270.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000749\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5910.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.734\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.00317\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-231.0\", \"ZT\": \"1.18\", \"formula\": \"Mg2Si0.999Bi0.001\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 3.538304389, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.66\", \"Average atomic mass (g/mol)\": \"25.63\", \"Scarcity (wt fraction/abundance)\": \"159900.0\", \"HHI (production)\": \"5058.0\", \"HHI (reserves)\": \"697.4\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"316.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00168\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"53400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.147\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.00158\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-217.0\", \"ZT\": \"2.09\", \"formula\": \"Mg2Si0.9985Bi0.0015\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 6.2785333333, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.29\", \"Average atomic mass (g/mol)\": \"25.66\", \"Scarcity (wt fraction/abundance)\": \"239600.0\", \"HHI (production)\": \"5058.0\", \"HHI (reserves)\": \"704.6\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"635.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00299\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"47100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.33\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000929\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-153.0\", \"ZT\": \"1.76\", \"formula\": \"Mg2Si0.997Bi0.003\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 5.2915931109, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.53\", \"Average atomic mass (g/mol)\": \"25.75\", \"Scarcity (wt fraction/abundance)\": \"477500.0\", \"HHI (production)\": \"5060.0\", \"HHI (reserves)\": \"725.9\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1080.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00252\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.521\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000621\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-121.0\", \"ZT\": \"1.66\", \"formula\": \"Mg2Si0.995Bi0.005\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 4.9674434783, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.29\", \"Average atomic mass (g/mol)\": \"25.87\", \"Scarcity (wt fraction/abundance)\": \"792100.0\", \"HHI (production)\": \"5061.0\", \"HHI (reserves)\": \"754.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1610.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00237\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.641\"}, {\"doi\": \"10.1039/C1JM10827A\", \"Electrical resistivity (\\u03a9cm)\": \"0.000569\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-125.0\", \"ZT\": \"1.92\", \"formula\": \"Mg2Si0.993Bi0.007\", \"comment\": \"\", \"synthesis\": \"mechanochemical, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Bux 2011\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 5.7666959578, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.4\", \"Average atomic mass (g/mol)\": \"25.99\", \"Scarcity (wt fraction/abundance)\": \"1104000.0\", \"HHI (production)\": \"5063.0\", \"HHI (reserves)\": \"781.9\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1760.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00275\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.682\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.00125\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-175.0\", \"ZT\": \"1.72\", \"formula\": \"Mg2Si0.98Bi0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 5.1514852446, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.6\", \"Average atomic mass (g/mol)\": \"26.77\", \"Scarcity (wt fraction/abundance)\": \"3061000.0\", \"HHI (production)\": \"5072.0\", \"HHI (reserves)\": \"957.2\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"802.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00245\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.38\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.00137\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-176.0\", \"ZT\": \"1.59\", \"formula\": \"Mg2Si0.6Ge0.4Bi0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 4.7589433577, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.94\", \"Average atomic mass (g/mol)\": \"32.68\", \"Scarcity (wt fraction/abundance)\": \"2694000.0\", \"HHI (production)\": \"5169.0\", \"HHI (reserves)\": \"1229.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"730.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00227\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.643\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.04\", \"Seebeck coefficient (\\u03bcCV/K)\": \"149.0\", \"ZT\": \"0.04\", \"formula\": \"Mg2Si0.98Ag0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.67\", \"Average atomic mass (g/mol)\": \"26.1\", \"Scarcity (wt fraction/abundance)\": \"353300.0\", \"HHI (production)\": \"4954.0\", \"HHI (reserves)\": \"699.7\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"25.2\", \"Power Factor (W/(K\\u00b2m))\": \"5.59e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.012\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"319.0\", \"ZT\": \"0.48\", \"formula\": \"Mg2Si0.6Ge0.4Ag0.02\", \"comment\": \"\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 1.4324176107, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.57\", \"Average atomic mass (g/mol)\": \"32.01\", \"Scarcity (wt fraction/abundance)\": \"493400.0\", \"HHI (production)\": \"5075.0\", \"HHI (reserves)\": \"1026.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"67.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000682\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"102000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.045\"}, {\"doi\": \"10.1063/1.2009828\", \"Electrical resistivity (\\u03a9cm)\": \"0.026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"311.0\", \"ZT\": \"0.26\", \"formula\": \"Ag9Tl1Te5\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kurosaki 2005\", \"Structure\": \"ICSD #71689, 300K\", \"marker\": \"{'radius': 0.7693715909, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.2\", \"Average atomic mass (g/mol)\": \"120.88\", \"Scarcity (wt fraction/abundance)\": \"358900000.0\", \"HHI (production)\": \"2408.0\", \"HHI (reserves)\": \"3201.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"4758.66\", \"Average atomic volume (\\u212b\\u00b3)\": \"27.349\", \"Atoms per unit cell\": \"174.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"37.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.000366\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"96700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.323\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00463\", \"Seebeck coefficient (\\u03bcCV/K)\": \"288.0\", \"ZT\": \"1.25\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"*kappa extrapolated\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 3.7620388769, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"216.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00179\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"82900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.184\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00742\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-219.0\", \"ZT\": \"0.45\", \"formula\": \"Ba8Ga18Ge28\", \"comment\": \"\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 1.3577527635, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.1\", \"Average atomic mass (g/mol)\": \"81.25\", \"Scarcity (wt fraction/abundance)\": \"335300.0\", \"HHI (production)\": \"4759.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"135.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000647\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.209\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.00694\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-138.0\", \"ZT\": \"0.19\", \"formula\": \"Ba8Ga16Sn30\", \"comment\": \"*value at 662 K\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #161949, 300K\", \"marker\": \"{'radius': 0.576259366, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"106.95\", \"Scarcity (wt fraction/abundance)\": \"284700.0\", \"HHI (production)\": \"3226.0\", \"HHI (reserves)\": \"1823.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1595.46\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.546\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"144.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000274\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.00141\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-139.0\", \"ZT\": \"0.96\", \"formula\": \"Sr8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #90177, 295K\", \"marker\": \"{'radius': 2.8775957447, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"73.99\", \"Scarcity (wt fraction/abundance)\": \"391300.0\", \"HHI (production)\": \"5141.0\", \"HHI (reserves)\": \"2089.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1233.18\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.837\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"709.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00137\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.00141\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-186.0\", \"ZT\": \"1.72\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 5.1525957447, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"709.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00245\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.1999.843362\", \"Electrical resistivity (\\u03a9cm)\": \"0.00187\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-111.0\", \"ZT\": \"0.46\", \"formula\": \"Ba8Ga16Si30\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kuznetsov 1999\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 1.3836417112, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.61\", \"Scarcity (wt fraction/abundance)\": \"20060.0\", \"HHI (production)\": \"4373.0\", \"HHI (reserves)\": \"1811.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"535.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000659\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.0038\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-267.0\", \"ZT\": \"1.31\", \"formula\": \"Mg2Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 3.9375828511, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.25\", \"Average atomic mass (g/mol)\": \"25.57\", \"Scarcity (wt fraction/abundance)\": \"27.34\", \"HHI (production)\": \"5057.0\", \"HHI (reserves)\": \"683.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"263.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00188\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"71300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.138\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00255\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-153.0\", \"ZT\": \"0.64\", \"formula\": \"Mg1.95Ca0.05Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.9247807361, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.8\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"27.02\", \"HHI (production)\": \"5023.0\", \"HHI (reserves)\": \"707.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"392.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000917\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.176\"}, {\"doi\": \"10.1016/j.jallcom.2007.09.101\", \"Electrical resistivity (\\u03a9cm)\": \"0.00275\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-130.0\", \"ZT\": \"0.43\", \"formula\": \"Mg1.9Ca0.1Si1\", \"comment\": \"\", \"synthesis\": \"melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zhang 2008\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.2900763359, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.8\", \"Average atomic mass (g/mol)\": \"26.09\", \"Scarcity (wt fraction/abundance)\": \"26.71\", \"HHI (production)\": \"4990.0\", \"HHI (reserves)\": \"730.6\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"364.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000614\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.163\"}, {\"doi\": \"10.1016/j.jcrysgro.2006.10.270\", \"Electrical resistivity (\\u03a9cm)\": \"0.00412\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-283.0\", \"ZT\": \"1.36\", \"formula\": \"Mg2Si1\", \"comment\": \"\", \"synthesis\": \"Bridgman method, Ar-H gas\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Akasaka 2007\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 4.0657405091, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.05\", \"Average atomic mass (g/mol)\": \"25.57\", \"Scarcity (wt fraction/abundance)\": \"27.34\", \"HHI (production)\": \"5057.0\", \"HHI (reserves)\": \"683.1\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"242.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00194\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"79900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.136\"}, {\"doi\": \"10.1038/nmat3275\", \"Electrical resistivity (\\u03a9cm)\": \"0.0042\", \"Seebeck coefficient (\\u03bcCV/K)\": \"201.0\", \"ZT\": \"0.67\", \"formula\": \"Cu2Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 2.02005, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.915\", \"Average atomic mass (g/mol)\": \"68.68\", \"Scarcity (wt fraction/abundance)\": \"7674000.0\", \"HHI (production)\": \"1825.0\", \"HHI (reserves)\": \"1672.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"238.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000962\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.444\"}, {\"doi\": \"10.1038/nmat3279\", \"Electrical resistivity (\\u03a9cm)\": \"0.00151\", \"Seebeck coefficient (\\u03bcCV/K)\": \"129.0\", \"ZT\": \"0.77\", \"formula\": \"Cu1.98Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 2.3143112583, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.45\", \"Average atomic mass (g/mol)\": \"68.72\", \"Scarcity (wt fraction/abundance)\": \"7721000.0\", \"HHI (production)\": \"1826.0\", \"HHI (reserves)\": \"1673.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"662.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0011\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.78\"}, {\"doi\": \"http://link.aip.org/link/doi/10.1063/1.1562337\", \"Electrical resistivity (\\u03a9cm)\": \"0.00231\", \"Seebeck coefficient (\\u03bcCV/K)\": \"197.0\", \"ZT\": \"1.17\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"flux (SrCl2), air\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Shikano 2003\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 3.5235149157, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"3.15\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"432.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00168\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.234\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.0099\", \"Seebeck coefficient (\\u03bcCV/K)\": \"147.0\", \"ZT\": \"0.15\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.4583264317, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.8\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"101.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000218\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.096\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00801\", \"Seebeck coefficient (\\u03bcCV/K)\": \"154.0\", \"ZT\": \"0.21\", \"formula\": \"Ca2.7Na0.3Co4O9\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.6188510617, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"30.93\", \"Scarcity (wt fraction/abundance)\": \"17330.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1745.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"125.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000295\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.107\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.0091\", \"Seebeck coefficient (\\u03bcCV/K)\": \"169.0\", \"ZT\": \"0.22\", \"formula\": \"Ca2.7Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.6594623419, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"34.41\", \"Scarcity (wt fraction/abundance)\": \"6713000.0\", \"HHI (production)\": \"2799.0\", \"HHI (reserves)\": \"2245.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"110.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000314\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.094\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.0085\", \"Seebeck coefficient (\\u03bcCV/K)\": \"173.0\", \"ZT\": \"0.25\", \"formula\": \"Ca2.4Na0.3Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.7391614724, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.8\", \"Average atomic mass (g/mol)\": \"34.09\", \"Scarcity (wt fraction/abundance)\": \"6776000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2239.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"118.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000352\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.112\"}, {\"doi\": \"http://jjap.jsap.jp/link?JJAP/43/L540/\", \"Electrical resistivity (\\u03a9cm)\": \"0.00344\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-185.0\", \"ZT\": \"0.7\", \"formula\": \"Sr0.9Y0.1Ti1O3\", \"comment\": \"*kappa estimated from  300K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Obara 2004\", \"Structure\": \"ICSD #181231, 300K\", \"marker\": \"{'radius': 2.0960985174, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"5.0\", \"Average atomic mass (g/mol)\": \"36.72\", \"Scarcity (wt fraction/abundance)\": \"2782.0\", \"HHI (production)\": \"2693.0\", \"HHI (reserves)\": \"1952.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.872\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"291.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000998\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.099\"}, {\"doi\": \"10.1016/j.jallcom.2003.07.016\", \"Electrical resistivity (\\u03a9cm)\": \"0.00273\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-163.0\", \"ZT\": \"0.68\", \"formula\": \"Ba0.3Sr0.6La0.1Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction , Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2004\", \"Structure\": \"ICSD #181231, 300K\", \"marker\": \"{'radius': 2.0437692308, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"1.91\", \"Average atomic mass (g/mol)\": \"40.7\", \"Scarcity (wt fraction/abundance)\": \"3096.0\", \"HHI (production)\": \"2709.0\", \"HHI (reserves)\": \"1946.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.872\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"366.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000973\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.328\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.102\", \"Seebeck coefficient (\\u03bcCV/K)\": \"292.0\", \"ZT\": \"0.06\", \"formula\": \"Cu1Rh1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.61\", \"Scarcity (wt fraction/abundance)\": \"518600000.0\", \"HHI (production)\": \"2265.0\", \"HHI (reserves)\": \"4717.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.775\", \"Power Factor (W/(K\\u00b2m))\": \"8.36e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"85500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.046\", \"Seebeck coefficient (\\u03bcCV/K)\": \"283.0\", \"ZT\": \"0.12\", \"formula\": \"Cu1Rh0.99Mg0.01O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.3672203057, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.42\", \"Scarcity (wt fraction/abundance)\": \"515400000.0\", \"HHI (production)\": \"2263.0\", \"HHI (reserves)\": \"4695.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000175\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"80100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"232.0\", \"ZT\": \"0.28\", \"formula\": \"Cu1Rh0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.8250394161, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.83\", \"Scarcity (wt fraction/abundance)\": \"505800000.0\", \"HHI (production)\": \"2259.0\", \"HHI (reserves)\": \"4627.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"73.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000393\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"53800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.00299\", \"Seebeck coefficient (\\u03bcCV/K)\": \"145.0\", \"ZT\": \"0.49\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 1.4746361538, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"334.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000702\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.249\", \"Seebeck coefficient (\\u03bcCV/K)\": \"412.0\", \"ZT\": \"0.05\", \"formula\": \"Ca3Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.745\", \"Average atomic mass (g/mol)\": \"73.21\", \"Scarcity (wt fraction/abundance)\": \"3564000.0\", \"HHI (production)\": \"6623.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.023\", \"Power Factor (W/(K\\u00b2m))\": \"6.82e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"170000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00922\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"248.0\", \"ZT\": \"0.25\", \"formula\": \"Ca2.97Na0.03Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.7509209302, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.84\", \"Average atomic mass (g/mol)\": \"73.14\", \"Scarcity (wt fraction/abundance)\": \"3567000.0\", \"HHI (production)\": \"6622.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"58.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000358\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"61500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.118\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"233.0\", \"ZT\": \"0.28\", \"formula\": \"Ca2.94Na0.06Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.8261369565, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.86\", \"Average atomic mass (g/mol)\": \"73.07\", \"Scarcity (wt fraction/abundance)\": \"3571000.0\", \"HHI (production)\": \"6621.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"72.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000393\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"54300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.144\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"215.0\", \"ZT\": \"0.27\", \"formula\": \"Ca2.85Na0.15Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.7956762295, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.84\", \"Average atomic mass (g/mol)\": \"72.85\", \"Scarcity (wt fraction/abundance)\": \"3582000.0\", \"HHI (production)\": \"6618.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"82.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000379\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"46200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.167\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-181.0\", \"ZT\": \"0.19\", \"formula\": \"Fe0.998Co0.002Si2\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.5568646829, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.9\", \"Average atomic mass (g/mol)\": \"37.34\", \"Scarcity (wt fraction/abundance)\": \"48.87\", \"HHI (production)\": \"3570.0\", \"HHI (reserves)\": \"1187.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"81.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000265\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"32600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.028\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.024\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-287.0\", \"ZT\": \"0.24\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.04O0.06\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.72072875, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.95\", \"Average atomic mass (g/mol)\": \"37.6\", \"Scarcity (wt fraction/abundance)\": \"1051.0\", \"HHI (production)\": \"3739.0\", \"HHI (reserves)\": \"1227.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"41.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000343\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"82400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.018\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.052\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-222.0\", \"ZT\": \"0.07\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.12O0.18\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.96\", \"Average atomic mass (g/mol)\": \"38.06\", \"Scarcity (wt fraction/abundance)\": \"2834.0\", \"HHI (production)\": \"4040.0\", \"HHI (reserves)\": \"1297.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"19.3\", \"Power Factor (W/(K\\u00b2m))\": \"9.51e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"49300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.011\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.235\", \"Seebeck coefficient (\\u03bcCV/K)\": \"390.0\", \"ZT\": \"0.05\", \"formula\": \"Ca5Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.764\", \"Average atomic mass (g/mol)\": \"75.76\", \"Scarcity (wt fraction/abundance)\": \"3709000.0\", \"HHI (production)\": \"6736.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.257\", \"Power Factor (W/(K\\u00b2m))\": \"6.48e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"152000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00952\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"262.0\", \"ZT\": \"0.26\", \"formula\": \"Ca4.95Na0.05Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 0.7945992762, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.833\", \"Average atomic mass (g/mol)\": \"75.7\", \"Scarcity (wt fraction/abundance)\": \"3712000.0\", \"HHI (production)\": \"6735.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"55.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000378\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"68500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.113\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.00733\", \"Seebeck coefficient (\\u03bcCV/K)\": \"201.0\", \"ZT\": \"0.39\", \"formula\": \"Ca4.75Na0.25Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 1.1551615825, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.82\", \"Average atomic mass (g/mol)\": \"75.43\", \"Scarcity (wt fraction/abundance)\": \"3725000.0\", \"HHI (production)\": \"6732.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"136.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00055\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.284\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.18\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-370.0\", \"ZT\": \"0.05\", \"formula\": \"Fe1.98Ti0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.91\", \"Scarcity (wt fraction/abundance)\": \"13.87\", \"HHI (production)\": \"1837.0\", \"HHI (reserves)\": \"1111.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"55600.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.63e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"137000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.094\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-323.0\", \"ZT\": \"0.08\", \"formula\": \"Fe1.96Ti0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.7\", \"Average atomic mass (g/mol)\": \"31.87\", \"Scarcity (wt fraction/abundance)\": \"14.74\", \"HHI (production)\": \"1829.0\", \"HHI (reserves)\": \"1112.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"106000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000111\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"104000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"38.6\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.076\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-292.0\", \"ZT\": \"0.08\", \"formula\": \"Fe1.94Ti0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.34\", \"Average atomic mass (g/mol)\": \"31.84\", \"Scarcity (wt fraction/abundance)\": \"15.62\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"1113.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"132000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000112\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"85300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"51.9\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.213\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-374.0\", \"ZT\": \"0.05\", \"formula\": \"Fe1.98Sn0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.19\", \"Scarcity (wt fraction/abundance)\": \"6569.0\", \"HHI (production)\": \"1853.0\", \"HHI (reserves)\": \"1117.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46900.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.56e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"140000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.107\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-318.0\", \"ZT\": \"0.07\", \"formula\": \"Fe1.96Sn0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.22\", \"Average atomic mass (g/mol)\": \"32.44\", \"Scarcity (wt fraction/abundance)\": \"13020.0\", \"HHI (production)\": \"1860.0\", \"HHI (reserves)\": \"1122.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"93000.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.4e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"101000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"37.7\"}, {\"doi\": \"10.1016/j.jssc.2011.02.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.000878\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-53.0\", \"ZT\": \"0.23\", \"formula\": \"Ba7Sr1Al16Si30\", \"comment\": \"\", \"synthesis\": \"flux (Al), dynamic vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Roudebush 2011\", \"Structure\": \"ICSD #380509, 90K\", \"marker\": \"{'radius': 0.6757514879, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.46\", \"Average atomic mass (g/mol)\": \"43.02\", \"Scarcity (wt fraction/abundance)\": \"1088.0\", \"HHI (production)\": \"3387.0\", \"HHI (reserves)\": \"1633.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1193.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.691\", \"Atoms per unit cell\": \"55.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1140.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000322\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2830.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.791\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.024\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-100.0\", \"ZT\": \"0.03\", \"formula\": \"Nd2Cu1O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.19\", \"Average atomic mass (g/mol)\": \"59.43\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6889.0\", \"HHI (reserves)\": \"2479.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"41.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.08e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9940.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.017\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-99.0\", \"ZT\": \"0.03\", \"formula\": \"Nd2Cu0.98Ni0.02O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.25\", \"Average atomic mass (g/mol)\": \"59.42\", \"Scarcity (wt fraction/abundance)\": \"20980.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2480.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.3\", \"Power Factor (W/(K\\u00b2m))\": \"4.49e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.015\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.076\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-176.0\", \"ZT\": \"0.03\", \"formula\": \"Nd2Cu0.98Zn0.02O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.22\", \"Average atomic mass (g/mol)\": \"59.44\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2481.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"13.1\", \"Power Factor (W/(K\\u00b2m))\": \"4.04e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00429\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.000802\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-68.0\", \"ZT\": \"0.4\", \"formula\": \"La3Te3.8Sb0.2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 1.1965705736, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.72\", \"Average atomic mass (g/mol)\": \"132.28\", \"Scarcity (wt fraction/abundance)\": \"523800000.0\", \"HHI (production)\": \"5987.0\", \"HHI (reserves)\": \"4082.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1250.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00057\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4570.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.783\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00187\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-87.0\", \"ZT\": \"0.28\", \"formula\": \"La3Te3.65Sb0.35\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.8539071658, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.98\", \"Average atomic mass (g/mol)\": \"132.15\", \"Scarcity (wt fraction/abundance)\": \"503700000.0\", \"HHI (production)\": \"6089.0\", \"HHI (reserves)\": \"4051.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"535.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000407\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.461\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00721\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-159.0\", \"ZT\": \"0.25\", \"formula\": \"La3Te3.35Sb0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.739121068, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.17\", \"Average atomic mass (g/mol)\": \"131.9\", \"Scarcity (wt fraction/abundance)\": \"463400000.0\", \"HHI (production)\": \"6293.0\", \"HHI (reserves)\": \"3990.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"139.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000352\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.202\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00437\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-131.0\", \"ZT\": \"0.27\", \"formula\": \"La3Te3.35Bi0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.8196420137, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.56\", \"Average atomic mass (g/mol)\": \"140.0\", \"Scarcity (wt fraction/abundance)\": \"444300000.0\", \"HHI (production)\": \"6025.0\", \"HHI (reserves)\": \"4313.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"229.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00039\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.251\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.000802\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-58.0\", \"ZT\": \"0.29\", \"formula\": \"La2.99Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 0.8687401496, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.84\", \"Average atomic mass (g/mol)\": \"132.44\", \"Scarcity (wt fraction/abundance)\": \"551400000.0\", \"HHI (production)\": \"5846.0\", \"HHI (reserves)\": \"4124.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1250.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000414\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3320.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.75\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00425\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-159.0\", \"ZT\": \"0.42\", \"formula\": \"La2.74Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 1.2491788235, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.0\", \"Average atomic mass (g/mol)\": \"132.2\", \"Scarcity (wt fraction/abundance)\": \"572900000.0\", \"HHI (production)\": \"5704.0\", \"HHI (reserves)\": \"4163.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"235.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000595\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.402\"}, {\"doi\": \"10.1021/nl202439h\", \"Electrical resistivity (\\u03a9cm)\": \"0.065\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-268.0\", \"ZT\": \"0.08\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"microwave solvothermal, air\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Jood 2011\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.283\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"15.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.00011\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"71800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.011\"}, {\"doi\": \"10.1063/1.3291563\", \"Electrical resistivity (\\u03a9cm)\": \"0.0014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-201.0\", \"ZT\": \"2.02\", \"formula\": \"Sr0.61Ba0.39Nb2O6\", \"comment\": \"*values at 550 K, extrapolated from 516 K, values parallel to c axis\", \"synthesis\": \"Czochralski method, anneal PO<sub>2</sub> 10<sup>-14</sup>\", \"form\": \"single crystal\", \"temperature\": \"700\", \"author\": \"Lee 2010\", \"Structure\": \"ICSD #96013, 300K\", \"marker\": \"{'radius': 6.06015, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.172\", \"Average atomic mass (g/mol)\": \"43.2\", \"Scarcity (wt fraction/abundance)\": \"26540.0\", \"HHI (production)\": \"5182.0\", \"HHI (reserves)\": \"5061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"610.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.564\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"714.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00289\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.562\"}, {\"doi\": \"10.1557/jmr.2010.78\", \"Electrical resistivity (\\u03a9cm)\": \"0.008\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-216.0\", \"ZT\": \"0.41\", \"formula\": \"Sr0.61Ba0.39Nb2O6\", \"comment\": \"*values at 550 K, extrapolated from 516 K, values parallel to c axis\", \"synthesis\": \"templated grain growth, air, anneal PO<sub>2</sub> 10<sup>-14</sup>\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Lee 2011\", \"Structure\": \"ICSD #96013, 300K\", \"marker\": \"{'radius': 1.22472, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.172\", \"Average atomic mass (g/mol)\": \"43.2\", \"Scarcity (wt fraction/abundance)\": \"26540.0\", \"HHI (production)\": \"5182.0\", \"HHI (reserves)\": \"5061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"610.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.564\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"125.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000583\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"46700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.098\"}, {\"doi\": \"10.1021/nl8026795\", \"Electrical resistivity (\\u03a9cm)\": \"0.00179\", \"Seebeck coefficient (\\u03bcCV/K)\": \"191.0\", \"ZT\": \"1.44\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"ball milling, hot-pressed nanopowders\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Joshi 2008\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 4.3089708512, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"2.566\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"560.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00205\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.372\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.00212\", \"Seebeck coefficient (\\u03bcCV/K)\": \"239.0\", \"ZT\": \"1.88\", \"formula\": \"Pb0.96Sr0.4Te1Na0.2\", \"comment\": \"\", \"synthesis\": \"sparks plasma sintering\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 5.64983811, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.18\", \"Average atomic mass (g/mol)\": \"143.03\", \"Scarcity (wt fraction/abundance)\": \"348500000.0\", \"HHI (production)\": \"2897.0\", \"HHI (reserves)\": \"2980.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"471.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00269\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"57100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.682\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.00301\", \"Seebeck coefficient (\\u03bcCV/K)\": \"263.0\", \"ZT\": \"1.61\", \"formula\": \"Pb0.98Sr0.2Te1Na0.1\", \"comment\": \"\", \"synthesis\": \"melting\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 4.82246268, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.03\", \"Average atomic mass (g/mol)\": \"153.72\", \"Scarcity (wt fraction/abundance)\": \"364100000.0\", \"HHI (production)\": \"2843.0\", \"HHI (reserves)\": \"2981.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"332.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0023\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"69200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.551\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.00225\", \"Seebeck coefficient (\\u03bcCV/K)\": \"236.0\", \"ZT\": \"1.73\", \"formula\": \"Pb0.98Te1Na0.2\", \"comment\": \"\", \"synthesis\": \"melting\", \"form\": \"polycrystalline\", \"temperature\": \"700\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 5.19309504, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.44\", \"Average atomic mass (g/mol)\": \"153.79\", \"Scarcity (wt fraction/abundance)\": \"380700000.0\", \"HHI (production)\": \"2761.0\", \"HHI (reserves)\": \"2963.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"444.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00247\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"55700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.527\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.177\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-280.0\", \"ZT\": \"0.04\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5.634\", \"Power Factor (W/(K\\u00b2m))\": \"4.41e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"78300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-190.0\", \"ZT\": \"0.09\", \"formula\": \"Ca0.98La0.02Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82210, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.0\", \"Scarcity (wt fraction/abundance)\": \"917.3\", \"HHI (production)\": \"1996.0\", \"HHI (reserves)\": \"1310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.74\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.387\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.3\", \"Power Factor (W/(K\\u00b2m))\": \"8.8e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-160.0\", \"ZT\": \"0.12\", \"formula\": \"Ca0.96La0.04Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82209, 300K\", \"marker\": \"{'radius': 0.3460610931, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.39\", \"Scarcity (wt fraction/abundance)\": \"1423.0\", \"HHI (production)\": \"2128.0\", \"HHI (reserves)\": \"1343.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.49\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.424\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"45.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000115\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-136.0\", \"ZT\": \"0.1\", \"formula\": \"Ca0.94La0.06Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82208, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.79\", \"Scarcity (wt fraction/abundance)\": \"1915.0\", \"HHI (production)\": \"2255.0\", \"HHI (reserves)\": \"1376.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.24\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.462\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"53.1\", \"Power Factor (W/(K\\u00b2m))\": \"9.78e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jmst.org/EN/Y2009/V25/I04/0535\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-141.0\", \"ZT\": \"0.13\", \"formula\": \"Ca0.92La0.08Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2009\", \"Structure\": \"ICSD #82207, 300K\", \"marker\": \"{'radius': 0.3790584895, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"2394.0\", \"HHI (production)\": \"2380.0\", \"HHI (reserves)\": \"1407.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.497\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"63.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000126\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"14.6\", \"Seebeck coefficient (\\u03bcCV/K)\": \"643.0\", \"ZT\": \"0.00282\", \"formula\": \"Ni1O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.35\", \"Scarcity (wt fraction/abundance)\": \"6477.0\", \"HHI (production)\": \"883.5\", \"HHI (reserves)\": \"1269.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.068\", \"Power Factor (W/(K\\u00b2m))\": \"2.82e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"413000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.047\", \"Seebeck coefficient (\\u03bcCV/K)\": \"262.0\", \"ZT\": \"0.15\", \"formula\": \"Li0.0024Ni0.9976O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.4432496959, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"8.444\", \"Average atomic mass (g/mol)\": \"37.28\", \"Scarcity (wt fraction/abundance)\": \"6484.0\", \"HHI (production)\": \"883.7\", \"HHI (reserves)\": \"1270.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000148\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"68900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0062\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"207.0\", \"ZT\": \"0.15\", \"formula\": \"Li0.0066Ni0.9944O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.4498804334, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"5.305\", \"Average atomic mass (g/mol)\": \"37.19\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"884.2\", \"HHI (reserves)\": \"1270.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"35.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.00015\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.016\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.00666\", \"Seebeck coefficient (\\u03bcCV/K)\": \"105.0\", \"ZT\": \"0.17\", \"formula\": \"Li0.0184Ni0.9816O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.4981869156, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"36.87\", \"Scarcity (wt fraction/abundance)\": \"6533.0\", \"HHI (production)\": \"885.3\", \"HHI (reserves)\": \"1271.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"150.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000166\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1143/JJAP.38.L1336\", \"Electrical resistivity (\\u03a9cm)\": \"0.00387\", \"Seebeck coefficient (\\u03bcCV/K)\": \"79.0\", \"ZT\": \"0.16\", \"formula\": \"Li0.0242Ni0.9758O1\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Shin 1999\", \"Structure\": \"ICSD #9866, 300K\", \"marker\": \"{'radius': 0.4893224196, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.55\", \"Average atomic mass (g/mol)\": \"36.72\", \"Scarcity (wt fraction/abundance)\": \"6552.0\", \"HHI (production)\": \"885.9\", \"HHI (reserves)\": \"1272.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"72.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.116\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"258.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000163\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6320.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.247\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.111\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-407.0\", \"ZT\": \"0.15\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"Extrapolated from 972 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.4490233235, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.679\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.044\", \"Power Factor (W/(K\\u00b2m))\": \"0.00015\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"165000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.013\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.027\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-205.0\", \"ZT\": \"0.16\", \"formula\": \"Ca0.98Bi0.02Mn0.98Nb0.02O3\", \"comment\": \"Extrapolated from 972 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.4740493661, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.736\", \"Average atomic mass (g/mol)\": \"29.43\", \"Scarcity (wt fraction/abundance)\": \"1672000.0\", \"HHI (production)\": \"2034.0\", \"HHI (reserves)\": \"1500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"37.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000158\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.053\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-172.0\", \"ZT\": \"0.2\", \"formula\": \"Ca0.9Bi0.1Mn0.9Nb0.1O3\", \"comment\": \"Extrapolated from 972 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.6123036534, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.687\", \"Average atomic mass (g/mol)\": \"32.74\", \"Scarcity (wt fraction/abundance)\": \"7513000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"2282.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"68.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000204\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.099\"}, {\"doi\": \"10.1016/j.jallcom.2009.08.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.0083\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-93.0\", \"ZT\": \"0.1\", \"formula\": \"Ca0.9Bi0.1Mn0.9Nb0.1O3\", \"comment\": \"Extrapolated from 972 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2009\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.3102475345, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.74\", \"Scarcity (wt fraction/abundance)\": \"7513000.0\", \"HHI (production)\": \"2638.0\", \"HHI (reserves)\": \"2282.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"120.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000103\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8590.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/jmr.2011.140\", \"Electrical resistivity (\\u03a9cm)\": \"0.031\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-248.0\", \"ZT\": \"0.2\", \"formula\": \"Ca1Mn0.98Nb0.02O3\", \"comment\": \"\", \"synthesis\": \"Ultrasonic Spray Pyrolysis\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Populoh 2011\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.5985706888, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.381\", \"Average atomic mass (g/mol)\": \"28.75\", \"Scarcity (wt fraction/abundance)\": \"1087.0\", \"HHI (production)\": \"1950.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"32.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.0002\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"61600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.057\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-214.0\", \"ZT\": \"0.16\", \"formula\": \"Ca1Mn0.98Ru0.02O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.4893991759, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"28.79\", \"Scarcity (wt fraction/abundance)\": \"14040000.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"1366.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"35.7\", \"Power Factor (W/(K\\u00b2m))\": \"0.000163\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"45700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-153.0\", \"ZT\": \"0.18\", \"formula\": \"Ca1Mn0.96Ru0.04O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.552266392, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.882\", \"Average atomic mass (g/mol)\": \"28.97\", \"Scarcity (wt fraction/abundance)\": \"27910000.0\", \"HHI (production)\": \"1904.0\", \"HHI (reserves)\": \"1456.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"78.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000184\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.067\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-145.0\", \"ZT\": \"0.18\", \"formula\": \"Ca1Mn0.94Ru0.06O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #166044, 298K\", \"marker\": \"{'radius': 0.5501796875, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.16\", \"Scarcity (wt fraction/abundance)\": \"41600000.0\", \"HHI (production)\": \"1925.0\", \"HHI (reserves)\": \"1544.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.41\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"87.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000183\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00674\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-102.0\", \"ZT\": \"0.15\", \"formula\": \"Ca1Mn0.9Ru0.1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.461613659, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.53\", \"Scarcity (wt fraction/abundance)\": \"68460000.0\", \"HHI (production)\": \"1966.0\", \"HHI (reserves)\": \"1717.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"148.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000154\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0025-5408(02)00997-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00505\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-68.0\", \"ZT\": \"0.09\", \"formula\": \"Ca1Mn0.82Ru0.18O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2003\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.26\", \"Scarcity (wt fraction/abundance)\": \"120200000.0\", \"HHI (production)\": \"2045.0\", \"HHI (reserves)\": \"2051.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"198.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.13e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4610.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.023\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-235.0\", \"ZT\": \"0.24\", \"formula\": \"Ca1Gd0.98Mn0.02O3\", \"comment\": \"Extrapolated from 926 K\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.731797148, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.66\", \"Scarcity (wt fraction/abundance)\": \"111100.0\", \"HHI (production)\": \"6744.0\", \"HHI (reserves)\": \"2336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"44.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000244\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"55400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-173.0\", \"ZT\": \"0.28\", \"formula\": \"Ca1Gd0.96Mn0.04O3\", \"comment\": \"Extrapolated from 926 K\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.8463353078, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.28\", \"Average atomic mass (g/mol)\": \"48.25\", \"Scarcity (wt fraction/abundance)\": \"109800.0\", \"HHI (production)\": \"6685.0\", \"HHI (reserves)\": \"2323.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"94.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000282\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.18\"}, {\"doi\": \"10.1111/j.1551-2916.2010.03673.x\", \"Electrical resistivity (\\u03a9cm)\": \"0.00887\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-145.0\", \"ZT\": \"0.24\", \"formula\": \"Ca1Gd0.94Mn0.06O3\", \"comment\": \"Extrapolated from 926 K\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Lan 2010\", \"Structure\": \"ICSD #165698, 293K\", \"marker\": \"{'radius': 0.7088164318, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.945\", \"Average atomic mass (g/mol)\": \"47.84\", \"Scarcity (wt fraction/abundance)\": \"108400.0\", \"HHI (production)\": \"6625.0\", \"HHI (reserves)\": \"2310.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.518\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"113.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000236\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.141\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00204\", \"Seebeck coefficient (\\u03bcCV/K)\": \"40.0\", \"ZT\": \"0.08\", \"formula\": \"Nd1.4Bi0.6Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78129, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"58.31\", \"Scarcity (wt fraction/abundance)\": \"326600000.0\", \"HHI (production)\": \"5126.0\", \"HHI (reserves)\": \"4765.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1102.66\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.53\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"491.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.84e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00153\", \"Seebeck coefficient (\\u03bcCV/K)\": \"35.0\", \"ZT\": \"0.08\", \"formula\": \"Nd1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"60.67\", \"Scarcity (wt fraction/abundance)\": \"321300000.0\", \"HHI (production)\": \"4772.0\", \"HHI (reserves)\": \"5060.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"653.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.21e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1260.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00298\", \"Seebeck coefficient (\\u03bcCV/K)\": \"39.0\", \"ZT\": \"0.05\", \"formula\": \"Yb1.4Bi0.6Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"61.98\", \"Scarcity (wt fraction/abundance)\": \"307400000.0\", \"HHI (production)\": \"5384.0\", \"HHI (reserves)\": \"4668.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"336.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.1e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1520.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0167-577X(01)00317-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00181\", \"Seebeck coefficient (\\u03bcCV/K)\": \"36.0\", \"ZT\": \"0.07\", \"formula\": \"Yb1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zhou 2001\", \"Structure\": \"ICSD #78127, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"63.29\", \"Scarcity (wt fraction/abundance)\": \"308100000.0\", \"HHI (production)\": \"4966.0\", \"HHI (reserves)\": \"4980.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1098.72\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.485\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"552.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.1e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1290.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000687\", \"Seebeck coefficient (\\u03bcCV/K)\": \"12.0\", \"ZT\": \"0.02\", \"formula\": \"Bi2Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73787, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"66.55\", \"Scarcity (wt fraction/abundance)\": \"309700000.0\", \"HHI (production)\": \"3994.0\", \"HHI (reserves)\": \"5707.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1090.63\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.394\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1430.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.25e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"155.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00119\", \"Seebeck coefficient (\\u03bcCV/K)\": \"17.0\", \"ZT\": \"0.03\", \"formula\": \"Y0.5Bi1.5Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73790, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"61.1\", \"Scarcity (wt fraction/abundance)\": \"328200000.0\", \"HHI (production)\": \"4178.0\", \"HHI (reserves)\": \"5460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1079.79\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.27\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"830.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.5e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"298.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.002\", \"Seebeck coefficient (\\u03bcCV/K)\": \"17.0\", \"ZT\": \"0.01\", \"formula\": \"Y1Bi1Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73793, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.64\", \"Scarcity (wt fraction/abundance)\": \"350400000.0\", \"HHI (production)\": \"4398.0\", \"HHI (reserves)\": \"5165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1069.75\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.156\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"492.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.48e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"296.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(03)00080-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.084\", \"Seebeck coefficient (\\u03bcCV/K)\": \"17.0\", \"ZT\": \"0.000352\", \"formula\": \"Y2Ru2O7\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 2003\", \"Structure\": \"ICSD #73799, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"44.72\", \"Scarcity (wt fraction/abundance)\": \"410900000.0\", \"HHI (production)\": \"4999.0\", \"HHI (reserves)\": \"4357.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1040.8\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.827\", \"Atoms per unit cell\": \"88.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"11.6\", \"Power Factor (W/(K\\u00b2m))\": \"3.52e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"298.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.021\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-130.0\", \"ZT\": \"0.08\", \"formula\": \"Ca0.9Nd0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164747, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.382\", \"Average atomic mass (g/mol)\": \"30.69\", \"Scarcity (wt fraction/abundance)\": \"2894.0\", \"HHI (production)\": \"2525.0\", \"HHI (reserves)\": \"1444.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.546\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.9\", \"Power Factor (W/(K\\u00b2m))\": \"7.93e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.048\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-130.0\", \"ZT\": \"0.09\", \"formula\": \"Ca0.9Tb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164751, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.842\", \"Average atomic mass (g/mol)\": \"30.98\", \"Scarcity (wt fraction/abundance)\": \"96250.0\", \"HHI (production)\": \"2591.0\", \"HHI (reserves)\": \"1460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.02\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.451\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"54.4\", \"Power Factor (W/(K\\u00b2m))\": \"9.19e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.072\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-130.0\", \"ZT\": \"0.14\", \"formula\": \"Ca0.9Ho0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164753, 293K\", \"marker\": \"{'radius': 0.4058184294, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.239\", \"Average atomic mass (g/mol)\": \"31.1\", \"Scarcity (wt fraction/abundance)\": \"85220.0\", \"HHI (production)\": \"2618.0\", \"HHI (reserves)\": \"1467.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.44\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.422\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"80.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000135\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.087\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.00825\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-130.0\", \"ZT\": \"0.2\", \"formula\": \"Ca0.9Yb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 293K\", \"marker\": \"{'radius': 0.6145248255, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.588\", \"Average atomic mass (g/mol)\": \"31.26\", \"Scarcity (wt fraction/abundance)\": \"37270.0\", \"HHI (production)\": \"2653.0\", \"HHI (reserves)\": \"1475.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"121.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000205\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.186\"}, {\"doi\": \"10.1063/1.2362922\", \"Electrical resistivity (\\u03a9cm)\": \"0.083\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-321.0\", \"ZT\": \"0.12\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.3695281015, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.092\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"12.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000123\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"103000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.014\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-152.0\", \"ZT\": \"0.23\", \"formula\": \"Ca0.9Tb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69824, 300K\", \"marker\": \"{'radius': 0.6798625039, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.604\", \"Average atomic mass (g/mol)\": \"30.98\", \"Scarcity (wt fraction/abundance)\": \"96250.0\", \"HHI (production)\": \"2591.0\", \"HHI (reserves)\": \"1460.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.479\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"97.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000227\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"23200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.148\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00559\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-68.0\", \"ZT\": \"0.08\", \"formula\": \"Ca0.7Tb0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #69826, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.681\", \"Average atomic mass (g/mol)\": \"35.73\", \"Scarcity (wt fraction/abundance)\": \"249700.0\", \"HHI (production)\": \"3759.0\", \"HHI (reserves)\": \"1755.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.15\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.658\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"179.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.33e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4650.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.26\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-115.0\", \"ZT\": \"0.11\", \"formula\": \"Ca0.9Ho0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160306, 300K\", \"marker\": \"{'radius': 0.3401243715, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.471\", \"Average atomic mass (g/mol)\": \"31.1\", \"Scarcity (wt fraction/abundance)\": \"85220.0\", \"HHI (production)\": \"2618.0\", \"HHI (reserves)\": \"1467.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"209.04\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.452\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"86.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000113\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.143\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00423\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-65.0\", \"ZT\": \"0.1\", \"formula\": \"Ca0.7Ho0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.599\", \"Average atomic mass (g/mol)\": \"36.09\", \"Scarcity (wt fraction/abundance)\": \"219600.0\", \"HHI (production)\": \"3816.0\", \"HHI (reserves)\": \"1769.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"237.0\", \"Power Factor (W/(K\\u00b2m))\": \"9.91e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4190.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.361\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.0071\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-136.0\", \"ZT\": \"0.26\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #160308, 300K\", \"marker\": \"{'radius': 0.7764093222, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.629\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.615\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"141.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000259\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"18400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.211\"}, {\"doi\": \"10.1016/0022-4596(91)90248-G\", \"Electrical resistivity (\\u03a9cm)\": \"0.00707\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-61.0\", \"ZT\": \"0.05\", \"formula\": \"Ca0.7Y0.3Mn1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 1991\", \"Structure\": \"ICSD #97601, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.537\", \"Average atomic mass (g/mol)\": \"31.53\", \"Scarcity (wt fraction/abundance)\": \"5816.0\", \"HHI (production)\": \"3058.0\", \"HHI (reserves)\": \"1490.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"219.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.992\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"141.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.23e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.225\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000859\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-30.0\", \"ZT\": \"0.11\", \"formula\": \"Ba1Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.3181183764, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"78.5\", \"Scarcity (wt fraction/abundance)\": \"44820.0\", \"HHI (production)\": \"2535.0\", \"HHI (reserves)\": \"1822.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1160.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000106\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"910.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000601\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-34.0\", \"ZT\": \"0.19\", \"formula\": \"Ba0.8Sr0.2Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #94312, 300K\", \"marker\": \"{'radius': 0.5671337317, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"76.52\", \"Scarcity (wt fraction/abundance)\": \"45940.0\", \"HHI (production)\": \"2579.0\", \"HHI (reserves)\": \"1839.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"311.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.572\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1660.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000189\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1140.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000687\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-40.0\", \"ZT\": \"0.23\", \"formula\": \"Ba0.6Sr0.4Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151610, 1198K\", \"marker\": \"{'radius': 0.6886773926, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"74.53\", \"Scarcity (wt fraction/abundance)\": \"47120.0\", \"HHI (production)\": \"2625.0\", \"HHI (reserves)\": \"1856.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"79.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.902\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1460.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00023\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1580.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1023/A:1018515223271\", \"Electrical resistivity (\\u03a9cm)\": \"0.000935\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-52.0\", \"ZT\": \"0.29\", \"formula\": \"Ba0.4Sr0.6Pb1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (under oxygen)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Yasukawa 1997\", \"Structure\": \"ICSD #151610, 1198K\", \"marker\": \"{'radius': 0.8838844395, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"72.54\", \"Scarcity (wt fraction/abundance)\": \"48360.0\", \"HHI (production)\": \"2674.0\", \"HHI (reserves)\": \"1874.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"79.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.902\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1070.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000295\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2750.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/PROC-793-S3.3\", \"Electrical resistivity (\\u03a9cm)\": \"0.00622\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-27.0\", \"ZT\": \"0.01\", \"formula\": \"La1Ni1O3\", \"comment\": \"\", \"synthesis\": \"Evaporate nitrates (1173 K, air)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Funahashi 2003\", \"Structure\": \"ICSD #84933, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.12\", \"Scarcity (wt fraction/abundance)\": \"17470.0\", \"HHI (production)\": \"5693.0\", \"HHI (reserves)\": \"2221.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"339.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.314\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"161.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.17e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"731.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1557/PROC-793-S3.3\", \"Electrical resistivity (\\u03a9cm)\": \"0.00609\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-31.0\", \"ZT\": \"0.02\", \"formula\": \"La0.9Bi0.1Ni1O3\", \"comment\": \"\", \"synthesis\": \"Evaporate nitrates (1173 K, air)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Funahashi 2003\", \"Structure\": \"ICSD #84933, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"50.52\", \"Scarcity (wt fraction/abundance)\": \"4882000.0\", \"HHI (production)\": \"5452.0\", \"HHI (reserves)\": \"2483.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"339.43\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.314\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"164.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.56e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"948.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.2007.4569450\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-188.0\", \"ZT\": \"0.32\", \"formula\": \"Ca0.96Sm0.04Mn1O3\", \"comment\": \"\", \"synthesis\": \"Co-precipitation\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sanmathi 2007\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.9548744715, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.48\", \"Scarcity (wt fraction/abundance)\": \"6638.0\", \"HHI (production)\": \"2150.0\", \"HHI (reserves)\": \"1349.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"90.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000318\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1201/9781420049718.ch22\", \"Electrical resistivity (\\u03a9cm)\": \"0.00128\", \"Seebeck coefficient (\\u03bcCV/K)\": \"166.0\", \"ZT\": \"2.15\", \"formula\": \"Ag0.15Sb0.15Te1.15Ge0.85\", \"comment\": \"Extrapolated from 870 K\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Skrabek 1995\", \"Structure\": \"ICSD #2084, 300K\", \"marker\": \"{'radius': 6.4624111554, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.272\", \"Average atomic mass (g/mol)\": \"105.62\", \"Scarcity (wt fraction/abundance)\": \"605500000.0\", \"HHI (production)\": \"3762.0\", \"HHI (reserves)\": \"3810.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"479.59\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.973\", \"Atoms per unit cell\": \"15.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"784.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00215\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.842\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.00205\", \"Seebeck coefficient (\\u03bcCV/K)\": \"204.0\", \"ZT\": \"2.03\", \"formula\": \"Na0.02Pb1Te0.85Se0.15\", \"comment\": \"Extrapolated from 850 K\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 6.0766591224, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.189\", \"Average atomic mass (g/mol)\": \"162.36\", \"Scarcity (wt fraction/abundance)\": \"331500000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2827.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"487.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00203\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"41600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.999\"}, {\"doi\": \"10.1038/nature09996\", \"Electrical resistivity (\\u03a9cm)\": \"0.00198\", \"Seebeck coefficient (\\u03bcCV/K)\": \"197.0\", \"ZT\": \"1.96\", \"formula\": \"Na0.02Pb1Te0.75Se0.25\", \"comment\": \"Extrapolated from 850 K\", \"synthesis\": \"melted\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Pei 2011\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 5.8723217528, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.196\", \"Average atomic mass (g/mol)\": \"159.95\", \"Scarcity (wt fraction/abundance)\": \"297500000.0\", \"HHI (production)\": \"2736.0\", \"HHI (reserves)\": \"2721.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"504.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00196\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.029\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00414\", \"Seebeck coefficient (\\u03bcCV/K)\": \"273.0\", \"ZT\": \"1.8\", \"formula\": \"Si0.9Ge0.1\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"1000\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 5.3954391892, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.54\", \"Scarcity (wt fraction/abundance)\": \"153900.0\", \"HHI (production)\": \"4833.0\", \"HHI (reserves)\": \"1200.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"241.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0018\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"74500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00334\", \"Seebeck coefficient (\\u03bcCV/K)\": \"254.0\", \"ZT\": \"1.93\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"\", \"form\": \"nanoparticles\", \"temperature\": \"1000\", \"author\": \"Snedaker\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 5.7913824057, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"299.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00193\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"64500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.00295\", \"Seebeck coefficient (\\u03bcCV/K)\": \"248.0\", \"ZT\": \"2.09\", \"formula\": \"Si0.79936Ge0.19984B0.0008\", \"comment\": \"\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 6.2636654724, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"3.599\", \"Average atomic mass (g/mol)\": \"36.98\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4927.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"339.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00209\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"61600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.23\"}, {\"doi\": \"10.1063/1.348408\", \"Electrical resistivity (\\u03a9cm)\": \"0.0025\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-281.0\", \"ZT\": \"3.16\", \"formula\": \"Si0.7956Ge0.1989P0.0055\", \"comment\": \"\", \"synthesis\": \"Vacuum hot pressed\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Vining 1991\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 9.4902377296, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"3.666\", \"Average atomic mass (g/mol)\": \"36.96\", \"Scarcity (wt fraction/abundance)\": \"269600.0\", \"HHI (production)\": \"4914.0\", \"HHI (reserves)\": \"1369.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"399.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00316\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"79200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.266\"}, {\"doi\": \"10.1063/1.4765358\", \"Electrical resistivity (\\u03a9cm)\": \"0.0015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-155.0\", \"ZT\": \"1.6\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"Extrapolated from 872 K\", \"synthesis\": \"Magnetic levitation induction furnace\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Douglas 2012\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 4.805, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.71\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"667.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0016\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"24000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.211\"}, {\"doi\": \"10.1063/1.1502190\", \"Electrical resistivity (\\u03a9cm)\": \"0.00367\", \"Seebeck coefficient (\\u03bcCV/K)\": \"294.0\", \"ZT\": \"2.35\", \"formula\": \"Bi2Sr2Co2O8\", \"comment\": \"\", \"synthesis\": \"Solid state reaction + extra\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Funahashi 2002\", \"Structure\": \"ICSD #none, 300K\", \"marker\": \"{'radius': 7.0506741199, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.973\", \"Average atomic mass (g/mol)\": \"59.93\", \"Scarcity (wt fraction/abundance)\": \"29310000.0\", \"HHI (production)\": \"4016.0\", \"HHI (reserves)\": \"4061.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.53\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.59\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"273.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00235\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"86200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.337\"}, {\"doi\": \"10.1143/JJAP.39.L1127\", \"Electrical resistivity (\\u03a9cm)\": \"0.00138\", \"Seebeck coefficient (\\u03bcCV/K)\": \"207.0\", \"ZT\": \"3.12\", \"formula\": \"Ca2Co2O5\", \"comment\": \"\", \"synthesis\": \"melted\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Funahashi 2000\", \"Structure\": \"ICSD #55458, 300K\", \"marker\": \"{'radius': 9.3500202826, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.9\", \"Average atomic mass (g/mol)\": \"30.89\", \"Scarcity (wt fraction/abundance)\": \"15420.0\", \"HHI (production)\": \"2551.0\", \"HHI (reserves)\": \"1702.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"236.38\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.883\", \"Atoms per unit cell\": \"21.72\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"725.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00312\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"43000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.61\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.00117\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-66.0\", \"ZT\": \"0.38\", \"formula\": \"W1O2.9\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24736, 300K\", \"marker\": \"{'radius': 1.1307951384, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.601\", \"Average atomic mass (g/mol)\": \"59.04\", \"Scarcity (wt fraction/abundance)\": \"679600.0\", \"HHI (production)\": \"5675.0\", \"HHI (reserves)\": \"3532.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1066.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.328\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"853.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000377\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4420.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.578\"}, {\"doi\": \"www.mrl.ucsb.edu:8080/datamine/pc.jsp\", \"Electrical resistivity (\\u03a9cm)\": \"0.000305\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-34.0\", \"ZT\": \"0.38\", \"formula\": \"W1O2.722\", \"comment\": \"\", \"synthesis\": \"Spark Plasma Sintering\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kieslich\", \"Structure\": \"ICSD #24731, 300K\", \"marker\": \"{'radius': 1.1292631529, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.295\", \"Average atomic mass (g/mol)\": \"61.09\", \"Scarcity (wt fraction/abundance)\": \"688100.0\", \"HHI (production)\": \"5740.0\", \"HHI (reserves)\": \"3570.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"883.29\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.268\", \"Atoms per unit cell\": \"72.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3280.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000376\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1150.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"1.272\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"100.0\", \"ZT\": \"0.05\", \"formula\": \"La1.95Sr0.05Cu1O4\", \"comment\": \"Seebeck extrapolated from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78632, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.54\", \"Scarcity (wt fraction/abundance)\": \"20920.0\", \"HHI (production)\": \"6746.0\", \"HHI (reserves)\": \"2457.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"380.25\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.58\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"52.1\", \"Power Factor (W/(K\\u00b2m))\": \"5.21e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00818\", \"Seebeck coefficient (\\u03bcCV/K)\": \"30.0\", \"ZT\": \"0.01\", \"formula\": \"La1.9Sr0.1Cu1O4\", \"comment\": \"Seebeck estimated Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #78240, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.17\", \"Scarcity (wt fraction/abundance)\": \"20610.0\", \"HHI (production)\": \"6670.0\", \"HHI (reserves)\": \"2451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"378.4\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.514\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"122.0\", \"Power Factor (W/(K\\u00b2m))\": \"1.1e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00376\", \"Seebeck coefficient (\\u03bcCV/K)\": \"1.0\", \"ZT\": \"2.66e-05\", \"formula\": \"La1.85Sr0.15Cu1O4\", \"comment\": \"Seebeck extrapolated from Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"56.81\", \"Scarcity (wt fraction/abundance)\": \"20290.0\", \"HHI (production)\": \"6594.0\", \"HHI (reserves)\": \"2445.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"266.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.66e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevLett.69.2975\", \"Electrical resistivity (\\u03a9cm)\": \"0.00223\", \"Seebeck coefficient (\\u03bcCV/K)\": \"0.0\", \"ZT\": \"4.49e-07\", \"formula\": \"La1.725Sr0.28Cu1O4\", \"comment\": \"Seebeck estimated Zhou1996PRB, DOI: 10.1103/PhysRevB.54.12488\", \"synthesis\": \"Solid state reaction (O2 atmosphere)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Takagi 1992\", \"Structure\": \"ICSD #62608, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.92\", \"Scarcity (wt fraction/abundance)\": \"19470.0\", \"HHI (production)\": \"6396.0\", \"HHI (reserves)\": \"2431.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"190.07\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.576\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"449.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.49e-10\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"0.01\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c2jm16297k\", \"Electrical resistivity (\\u03a9cm)\": \"0.36\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-85.0\", \"ZT\": \"0.002\", \"formula\": \"Li1Mn2O4\", \"comment\": \"\", \"synthesis\": \"Solid state reaction (oxalates)\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sparks 2012\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.781\", \"Power Factor (W/(K\\u00b2m))\": \"2e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7190.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.053\", \"Seebeck coefficient (\\u03bcCV/K)\": \"325.0\", \"ZT\": \"0.2\", \"formula\": \"Cu1Fe0.9Cr0.1O2\", \"comment\": \"Extrapolated from 830 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #31918, 300K\", \"marker\": \"{'radius': 0.5951051409, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.75\", \"Scarcity (wt fraction/abundance)\": \"6756.0\", \"HHI (production)\": \"1683.0\", \"HHI (reserves)\": \"1344.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"136.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.412\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"18.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.000198\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"106000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00408\", \"Seebeck coefficient (\\u03bcCV/K)\": \"168.0\", \"ZT\": \"0.69\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 2.0742848443, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"245.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000691\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.072\", \"Seebeck coefficient (\\u03bcCV/K)\": \"355.0\", \"ZT\": \"0.17\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"Extrapolated from 900 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.52365381, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"13.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.000175\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"126000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"64.9\", \"Seebeck coefficient (\\u03bcCV/K)\": \"161.0\", \"ZT\": \"3.99e-05\", \"formula\": \"W1O3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.96\", \"Scarcity (wt fraction/abundance)\": \"674900.0\", \"HHI (production)\": \"5639.0\", \"HHI (reserves)\": \"3511.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.015\", \"Power Factor (W/(K\\u00b2m))\": \"3.99e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"36.4\", \"Seebeck coefficient (\\u03bcCV/K)\": \"114.0\", \"ZT\": \"3.56e-05\", \"formula\": \"W0.99O2.97Co0.02O0.03\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"57.65\", \"Scarcity (wt fraction/abundance)\": \"670200.0\", \"HHI (production)\": \"5615.0\", \"HHI (reserves)\": \"3500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.027\", \"Power Factor (W/(K\\u00b2m))\": \"3.56e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"15.9\", \"Seebeck coefficient (\\u03bcCV/K)\": \"126.0\", \"ZT\": \"9.93e-05\", \"formula\": \"W0.95O2.95Co0.1O0.15\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"55.45\", \"Scarcity (wt fraction/abundance)\": \"646800.0\", \"HHI (production)\": \"5484.0\", \"HHI (reserves)\": \"3437.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.063\", \"Power Factor (W/(K\\u00b2m))\": \"9.93e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s10854-011-0574-8\", \"Electrical resistivity (\\u03a9cm)\": \"35.7\", \"Seebeck coefficient (\\u03bcCV/K)\": \"124.0\", \"ZT\": \"4.32e-05\", \"formula\": \"W0.9O2.7Co0.2O0.3\", \"comment\": \"\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Dong 2012\", \"Structure\": \"ICSD #80053, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"54.94\", \"Scarcity (wt fraction/abundance)\": \"627100.0\", \"HHI (production)\": \"5394.0\", \"HHI (reserves)\": \"3402.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"422.94\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.217\", \"Atoms per unit cell\": \"32.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.028\", \"Power Factor (W/(K\\u00b2m))\": \"4.32e-08\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.084\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-282.0\", \"ZT\": \"0.09\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"Resistivity calculated from reported Seebeck, thermal conductivity, and zT\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"2.065\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"11.9\", \"Power Factor (W/(K\\u00b2m))\": \"9.44e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"79600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.014\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-245.0\", \"ZT\": \"0.32\", \"formula\": \"Ca1Yb0.05Mn0.95O3\", \"comment\": \"Resistivity extrapolated from 960 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9639330785, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.614\", \"Average atomic mass (g/mol)\": \"29.78\", \"Scarcity (wt fraction/abundance)\": \"19730.0\", \"HHI (production)\": \"2309.0\", \"HHI (reserves)\": \"1374.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"53.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000321\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"60000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.081\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00782\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-128.0\", \"ZT\": \"0.21\", \"formula\": \"Ca1Yb0.1Mn0.9O3\", \"comment\": \"Thermal conductivity extrapolated from 970 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.6317201619, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.583\", \"Average atomic mass (g/mol)\": \"30.96\", \"Scarcity (wt fraction/abundance)\": \"37590.0\", \"HHI (production)\": \"2722.0\", \"HHI (reserves)\": \"1465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"128.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000211\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.197\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.00596\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.17\", \"formula\": \"Ca1Yb0.15Mn0.85O3\", \"comment\": \"Thermal conductivity extrapolated from 970 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.5142646876, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.694\", \"Average atomic mass (g/mol)\": \"32.15\", \"Scarcity (wt fraction/abundance)\": \"54140.0\", \"HHI (production)\": \"3105.0\", \"HHI (reserves)\": \"1549.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"168.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000171\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.242\"}, {\"doi\": \"10.1109/ICT.2006.331291\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-25.0\", \"ZT\": \"0.00586\", \"formula\": \"Ca1Yb0.4Mn0.6O3\", \"comment\": \"Thermal conductivity extrapolated from 970 K\", \"synthesis\": \"Solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Flahaut 2006\", \"Structure\": \"ICSD #164755, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"121500.0\", \"HHI (production)\": \"4663.0\", \"HHI (reserves)\": \"1891.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"207.52\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.376\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"90.3\", \"Power Factor (W/(K\\u00b2m))\": \"5.86e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"650.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.023\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-223.0\", \"ZT\": \"0.22\", \"formula\": \"In2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 0.64802275, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.976\", \"Average atomic mass (g/mol)\": \"55.53\", \"Scarcity (wt fraction/abundance)\": \"4035000.0\", \"HHI (production)\": \"2843.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"43.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000216\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"49600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.036\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.0045\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-178.0\", \"ZT\": \"0.7\", \"formula\": \"In1.998Ge0.002O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 2.11039174, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.931\", \"Average atomic mass (g/mol)\": \"55.51\", \"Scarcity (wt fraction/abundance)\": \"4032000.0\", \"HHI (production)\": \"2844.0\", \"HHI (reserves)\": \"1741.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"222.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000703\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.185\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00168\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-119.0\", \"ZT\": \"0.85\", \"formula\": \"In1.994Ge0.006O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 2.5365804572, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.49\", \"Average atomic mass (g/mol)\": \"55.48\", \"Scarcity (wt fraction/abundance)\": \"4027000.0\", \"HHI (production)\": \"2846.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"594.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000846\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.415\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00143\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-108.0\", \"ZT\": \"0.82\", \"formula\": \"In1.985Ge0.015O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 2.460064677, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.536\", \"Average atomic mass (g/mol)\": \"55.4\", \"Scarcity (wt fraction/abundance)\": \"4016000.0\", \"HHI (production)\": \"2850.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"697.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00082\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.481\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00178\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-115.0\", \"ZT\": \"0.74\", \"formula\": \"In1.94Ge0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 2.2298082005, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.063\", \"Average atomic mass (g/mol)\": \"55.02\", \"Scarcity (wt fraction/abundance)\": \"3961000.0\", \"HHI (production)\": \"2869.0\", \"HHI (reserves)\": \"1737.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"562.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000743\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.448\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00209\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-117.0\", \"ZT\": \"0.66\", \"formula\": \"In1.9Ge0.1O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 1.9830674057, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.514\", \"Average atomic mass (g/mol)\": \"54.68\", \"Scarcity (wt fraction/abundance)\": \"3910000.0\", \"HHI (production)\": \"2887.0\", \"HHI (reserves)\": \"1734.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"479.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000661\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.465\"}, {\"doi\": \"10.1016/j.ssc.2007.12.033\", \"Electrical resistivity (\\u03a9cm)\": \"0.00267\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-110.0\", \"ZT\": \"0.45\", \"formula\": \"In1.8Ge0.2O3\", \"comment\": \"Thermal conductivity error is +/- 10%\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Berardan 2008\", \"Structure\": \"ICSD #14388, 300K\", \"marker\": \"{'radius': 1.3596078755, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"1.631\", \"Average atomic mass (g/mol)\": \"53.84\", \"Scarcity (wt fraction/abundance)\": \"3782000.0\", \"HHI (production)\": \"2932.0\", \"HHI (reserves)\": \"1727.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1035.51\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.944\", \"Atoms per unit cell\": \"80.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"374.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000453\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"12100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.56\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000984\", \"Seebeck coefficient (\\u03bcCV/K)\": \"16.0\", \"ZT\": \"0.03\", \"formula\": \"La1Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.17\", \"Scarcity (wt fraction/abundance)\": \"24200.0\", \"HHI (production)\": \"6184.0\", \"HHI (reserves)\": \"2502.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1020.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.5e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"246.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000951\", \"Seebeck coefficient (\\u03bcCV/K)\": \"19.0\", \"ZT\": \"0.04\", \"formula\": \"La0.99Sr0.01Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.06\", \"Scarcity (wt fraction/abundance)\": \"24100.0\", \"HHI (production)\": \"6158.0\", \"HHI (reserves)\": \"2500.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1050.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.62e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"344.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000916\", \"Seebeck coefficient (\\u03bcCV/K)\": \"18.0\", \"ZT\": \"0.03\", \"formula\": \"La0.98Sr0.02Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247225, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.96\", \"Scarcity (wt fraction/abundance)\": \"24010.0\", \"HHI (production)\": \"6132.0\", \"HHI (reserves)\": \"2499.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.73\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.136\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1090.0\", \"Power Factor (W/(K\\u00b2m))\": \"3.38e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"310.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000832\", \"Seebeck coefficient (\\u03bcCV/K)\": \"15.0\", \"ZT\": \"0.03\", \"formula\": \"La0.95Sr0.05Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247230, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.65\", \"Scarcity (wt fraction/abundance)\": \"23720.0\", \"HHI (production)\": \"6053.0\", \"HHI (reserves)\": \"2493.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"222.95\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.147\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1200.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.63e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"219.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jssc.2008.08.078\", \"Electrical resistivity (\\u03a9cm)\": \"0.000597\", \"Seebeck coefficient (\\u03bcCV/K)\": \"6.0\", \"ZT\": \"0.0051\", \"formula\": \"La0.8Sr0.2Co1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Iwasaki 2008\", \"Structure\": \"ICSD #247232, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"47.12\", \"Scarcity (wt fraction/abundance)\": \"22220.0\", \"HHI (production)\": \"5646.0\", \"HHI (reserves)\": \"2465.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"224.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.21\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1670.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.1e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30.5\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1021/cm060261t\", \"Electrical resistivity (\\u03a9cm)\": \"0.00458\", \"Seebeck coefficient (\\u03bcCV/K)\": \"164.0\", \"ZT\": \"0.59\", \"formula\": \"Yb14Mn1Sb11\", \"comment\": \"\", \"synthesis\": \"flux (Sn), Ar\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Brown 2006\", \"Structure\": \"ICSD #85638, 143K\", \"marker\": \"{'radius': 1.7651402623, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.715\", \"Average atomic mass (g/mol)\": \"146.81\", \"Scarcity (wt fraction/abundance)\": \"1966000.0\", \"HHI (production)\": \"8812.0\", \"HHI (reserves)\": \"3211.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"6058.93\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.129\", \"Atoms per unit cell\": \"208.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"218.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000588\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.745\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.024\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-219.0\", \"ZT\": \"0.2\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.59914964, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"41.8\", \"Power Factor (W/(K\\u00b2m))\": \"0.0002\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"47800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.011\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-205.0\", \"ZT\": \"0.38\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.1484786895, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"91.4\", \"Power Factor (W/(K\\u00b2m))\": \"0.000383\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"41900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00953\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-188.0\", \"ZT\": \"0.37\", \"formula\": \"Zn0.9925Al0.0075O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.1113216693, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"10740.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1618.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"105.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00037\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.00772\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-176.0\", \"ZT\": \"0.4\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.2005645005, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"130.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0004\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0815-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-208.0\", \"ZT\": \"0.25\", \"formula\": \"Zn0.97Al0.03O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Guilmeau 2009\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.7565806814, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.11\", \"Scarcity (wt fraction/abundance)\": \"10610.0\", \"HHI (production)\": \"1360.0\", \"HHI (reserves)\": \"1608.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"58.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000252\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"43100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.036\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-40.0\", \"ZT\": \"0.00454\", \"formula\": \"Sr1Mn0.98Mo0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.28\", \"Scarcity (wt fraction/abundance)\": \"10260.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"28.1\", \"Power Factor (W/(K\\u00b2m))\": \"4.54e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1610.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.progsolidstchem.2007.01.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.023\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-74.0\", \"ZT\": \"0.02\", \"formula\": \"Sr1Mn0.96Mo0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Hebert 2007\", \"Structure\": \"ICSD #157935, 350K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.44\", \"Scarcity (wt fraction/abundance)\": \"18890.0\", \"HHI (production)\": \"2515.0\", \"HHI (reserves)\": \"2089.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"234.85\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.742\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"43.6\", \"Power Factor (W/(K\\u00b2m))\": \"2.41e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5530.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00259\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-178.0\", \"ZT\": \"1.22\", \"formula\": \"Nb1Co1Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 3.6501975725, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"9.927\", \"Average atomic mass (g/mol)\": \"90.18\", \"Scarcity (wt fraction/abundance)\": \"221500.0\", \"HHI (production)\": \"4729.0\", \"HHI (reserves)\": \"4317.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"386.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00122\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.095\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00298\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-251.0\", \"ZT\": \"2.11\", \"formula\": \"Nb1Co1.05Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 6.3370956511, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"7.672\", \"Average atomic mass (g/mol)\": \"89.67\", \"Scarcity (wt fraction/abundance)\": \"219500.0\", \"HHI (production)\": \"4711.0\", \"HHI (reserves)\": \"4299.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"336.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00211\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"62900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.107\"}, {\"doi\": \"10.1063/1.2828713\", \"Electrical resistivity (\\u03a9cm)\": \"0.00242\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-199.0\", \"ZT\": \"1.64\", \"formula\": \"Nb1Co1.10Sn1\", \"comment\": \"\", \"synthesis\": \"Floating zone melting\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Kimura 2008\", \"Structure\": \"ICSD #102553, 300K\", \"marker\": \"{'radius': 4.9216081729, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.773\", \"Average atomic mass (g/mol)\": \"89.17\", \"Scarcity (wt fraction/abundance)\": \"217500.0\", \"HHI (production)\": \"4693.0\", \"HHI (reserves)\": \"4281.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.86\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.572\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"413.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00164\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"39800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.149\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-20.0\", \"ZT\": \"0.001\", \"formula\": \"Ca1Mn7O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.83\", \"Scarcity (wt fraction/abundance)\": \"636.4\", \"HHI (production)\": \"1400.0\", \"HHI (reserves)\": \"1370.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.7\", \"Power Factor (W/(K\\u00b2m))\": \"1e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"407.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.028\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-24.0\", \"ZT\": \"0.00211\", \"formula\": \"Ca1Mn6.5Cu0.5O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.05\", \"Scarcity (wt fraction/abundance)\": \"1387.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1359.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"35.5\", \"Power Factor (W/(K\\u00b2m))\": \"2.11e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"593.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.02\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-30.0\", \"ZT\": \"0.00447\", \"formula\": \"Ca1Mn6Cu1O12\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #200971, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.26\", \"Scarcity (wt fraction/abundance)\": \"2126.0\", \"HHI (production)\": \"1401.0\", \"HHI (reserves)\": \"1348.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"598.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.982\", \"Atoms per unit cell\": \"60.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"49.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.47e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"912.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.261\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-19.0\", \"ZT\": \"0.000144\", \"formula\": \"Li1Mn2O4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #89459, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"25.83\", \"Scarcity (wt fraction/abundance)\": \"2694.0\", \"HHI (production)\": \"1254.0\", \"HHI (reserves)\": \"1425.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"555.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"9.922\", \"Atoms per unit cell\": \"56.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"3.83\", \"Power Factor (W/(K\\u00b2m))\": \"1.44e-07\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"377.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1063/1.1687532\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-24.0\", \"ZT\": \"0.00443\", \"formula\": \"Pr0.5Ca0.5Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kobayashi 2004\", \"Structure\": \"ICSD #85650, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.69\", \"Scarcity (wt fraction/abundance)\": \"40990.0\", \"HHI (production)\": \"4428.0\", \"HHI (reserves)\": \"1928.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"221.92\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.096\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"78.5\", \"Power Factor (W/(K\\u00b2m))\": \"4.43e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"564.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000723\", \"Seebeck coefficient (\\u03bcCV/K)\": \"24.0\", \"ZT\": \"0.08\", \"formula\": \"Mo3Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"5.291\", \"Average atomic mass (g/mol)\": \"114.04\", \"Scarcity (wt fraction/abundance)\": \"639700000.0\", \"HHI (production)\": \"2718.0\", \"HHI (reserves)\": \"5052.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1380.0\", \"Power Factor (W/(K\\u00b2m))\": \"7.91e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"572.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.638\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.000833\", \"Seebeck coefficient (\\u03bcCV/K)\": \"21.0\", \"ZT\": \"0.05\", \"formula\": \"Mo6Te7S1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"4.61\", \"Average atomic mass (g/mol)\": \"107.22\", \"Scarcity (wt fraction/abundance)\": \"595400000.0\", \"HHI (production)\": \"2661.0\", \"HHI (reserves)\": \"4975.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1200.0\", \"Power Factor (W/(K\\u00b2m))\": \"5.35e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"446.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.635\"}, {\"doi\": \"10.1016/S0925-8388(02)01002-2\", \"Electrical resistivity (\\u03a9cm)\": \"0.001\", \"Seebeck coefficient (\\u03bcCV/K)\": \"15.0\", \"ZT\": \"0.02\", \"formula\": \"Mo6Te6S2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #644477, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.454\", \"Average atomic mass (g/mol)\": \"100.39\", \"Scarcity (wt fraction/abundance)\": \"545100000.0\", \"HHI (production)\": \"2596.0\", \"HHI (reserves)\": \"4888.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1039.77\", \"Average atomic volume (\\u212b\\u00b3)\": \"24.756\", \"Atoms per unit cell\": \"42.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1000.0\", \"Power Factor (W/(K\\u00b2m))\": \"2.14e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"214.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.706\"}, {\"doi\": \"10.1109/ICT.2006.331289\", \"Electrical resistivity (\\u03a9cm)\": \"0.00553\", \"Seebeck coefficient (\\u03bcCV/K)\": \"266.0\", \"ZT\": \"1.28\", \"formula\": \"Cu1Rh0.9Mg0.1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kuriyama 2006\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 3.8384525186, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"8.392\", \"Average atomic mass (g/mol)\": \"47.65\", \"Scarcity (wt fraction/abundance)\": \"485900000.0\", \"HHI (production)\": \"2250.0\", \"HHI (reserves)\": \"4486.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"181.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00128\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"70800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.053\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-167.0\", \"ZT\": \"0.21\", \"formula\": \"Sr2Ti0.8Nb0.2O4\", \"comment\": \"*seebeck, resistivity extrapolated from700 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.6275025, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"1.92\", \"Average atomic mass (g/mol)\": \"42.3\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3261.0\", \"HHI (reserves)\": \"2636.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"187.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.357\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"75.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000209\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.095\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00781\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-158.0\", \"ZT\": \"0.32\", \"formula\": \"Sr3Ti1.6Nb0.4O7\", \"comment\": \"*seebeck, resistivity extrapolated from700 K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162886, 300K\", \"marker\": \"{'radius': 0.9586176, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.14\", \"Average atomic mass (g/mol)\": \"40.72\", \"Scarcity (wt fraction/abundance)\": \"5611.0\", \"HHI (production)\": \"3187.0\", \"HHI (reserves)\": \"2641.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"305.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.708\", \"Atoms per unit cell\": \"24.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"128.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00032\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.146\"}, {\"doi\": \"10.1063/1.3117943\", \"Electrical resistivity (\\u03a9cm)\": \"0.00256\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-165.0\", \"ZT\": \"1.06\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Wang 2009\", \"Structure\": \"ICSD #162889, 15K\", \"marker\": \"{'radius': 3.18146517, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.14\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"240.63\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.032\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"390.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00106\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.303\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-285.0\", \"ZT\": \"0.44\", \"formula\": \"Sr0.95La0.05Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 1.3296784298, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"37.21\", \"Scarcity (wt fraction/abundance)\": \"2291.0\", \"HHI (production)\": \"2640.0\", \"HHI (reserves)\": \"1987.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"54.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000443\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"81200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00793\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-221.0\", \"ZT\": \"0.62\", \"formula\": \"Sr0.9La0.1Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65091, 300K\", \"marker\": \"{'radius': 1.8471128949, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.15\", \"Average atomic mass (g/mol)\": \"37.72\", \"Scarcity (wt fraction/abundance)\": \"3205.0\", \"HHI (production)\": \"2856.0\", \"HHI (reserves)\": \"2006.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.83\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.966\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"126.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000616\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.098\"}, {\"doi\": \"10.1016/S0925-8388(02)00972-6\", \"Electrical resistivity (\\u03a9cm)\": \"0.00238\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-158.0\", \"ZT\": \"1.05\", \"formula\": \"Sr0.8La0.2Ti1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2003\", \"Structure\": \"ICSD #65094, 300K\", \"marker\": \"{'radius': 3.1459058628, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"38.75\", \"Scarcity (wt fraction/abundance)\": \"4961.0\", \"HHI (production)\": \"3271.0\", \"HHI (reserves)\": \"2041.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.0\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"420.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00105\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00163\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-160.0\", \"ZT\": \"1.57\", \"formula\": \"Ti1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 4.7045855896, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.442\", \"Average atomic mass (g/mol)\": \"75.09\", \"Scarcity (wt fraction/abundance)\": \"236400.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1579.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"615.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00157\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"25500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.233\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00114\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-173.0\", \"ZT\": \"2.61\", \"formula\": \"Ti0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 7.823221638, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.292\", \"Average atomic mass (g/mol)\": \"75.24\", \"Scarcity (wt fraction/abundance)\": \"236100.0\", \"HHI (production)\": \"1890.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"875.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00261\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"29800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.339\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00096\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-174.0\", \"ZT\": \"3.16\", \"formula\": \"Ti0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 9.4915946439, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.975\", \"Average atomic mass (g/mol)\": \"75.39\", \"Scarcity (wt fraction/abundance)\": \"235900.0\", \"HHI (production)\": \"1918.0\", \"HHI (reserves)\": \"1638.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1040.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00316\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.425\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000726\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-143.0\", \"ZT\": \"2.8\", \"formula\": \"Ti0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #174568, 300K\", \"marker\": \"{'radius': 8.3990367392, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"5.492\", \"Average atomic mass (g/mol)\": \"75.84\", \"Scarcity (wt fraction/abundance)\": \"235200.0\", \"HHI (production)\": \"2004.0\", \"HHI (reserves)\": \"1726.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"208.21\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.351\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1380.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0028\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.612\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00159\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-213.0\", \"ZT\": \"2.85\", \"formula\": \"Zr1Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 8.5561075263, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.642\", \"Average atomic mass (g/mol)\": \"89.54\", \"Scarcity (wt fraction/abundance)\": \"200100.0\", \"HHI (production)\": \"2519.0\", \"HHI (reserves)\": \"1929.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"629.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00285\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"45300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.231\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.00121\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-211.0\", \"ZT\": \"3.66\", \"formula\": \"Zr0.99Nb0.01Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 10.9747135091, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.062\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200200.0\", \"HHI (production)\": \"2537.0\", \"HHI (reserves)\": \"1950.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"823.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00366\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"44400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.331\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000952\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-196.0\", \"ZT\": \"4.05\", \"formula\": \"Zr0.98Nb0.02Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 12.1351853416, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.208\", \"Average atomic mass (g/mol)\": \"89.55\", \"Scarcity (wt fraction/abundance)\": \"200400.0\", \"HHI (production)\": \"2554.0\", \"HHI (reserves)\": \"1972.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1050.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00405\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.413\"}, {\"doi\": \"10.1016/j.jallcom.2008.02.041\", \"Electrical resistivity (\\u03a9cm)\": \"0.000587\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-151.0\", \"ZT\": \"3.87\", \"formula\": \"Zr0.95Nb0.05Ni1Sn1\", \"comment\": \"\", \"synthesis\": \"arc-melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2009\", \"Structure\": \"ICSD #646828, 300K\", \"marker\": \"{'radius': 11.6172725131, 'lineColor': 'rgba(115,44,123,.8)', 'fillColor': 'rgba(115,44,123,0)'}\", \"Thermal conductivity (W/mK)\": \"6.242\", \"Average atomic mass (g/mol)\": \"89.57\", \"Scarcity (wt fraction/abundance)\": \"200900.0\", \"HHI (production)\": \"2608.0\", \"HHI (reserves)\": \"2036.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"226.87\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.906\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1700.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00387\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"22700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.667\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.026\", \"Seebeck coefficient (\\u03bcCV/K)\": \"119.0\", \"ZT\": \"0.05\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"38.4\", \"Power Factor (W/(K\\u00b2m))\": \"5.4e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"14100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"124.0\", \"ZT\": \"0.08\", \"formula\": \"La0.05Ca2.85Co3.8O8.55\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.6\", \"Scarcity (wt fraction/abundance)\": \"17300.0\", \"HHI (production)\": \"2612.0\", \"HHI (reserves)\": \"1776.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"52.4\", \"Power Factor (W/(K\\u00b2m))\": \"8.04e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.015\", \"Seebeck coefficient (\\u03bcCV/K)\": \"127.0\", \"ZT\": \"0.11\", \"formula\": \"La0.3Ca2.7Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.3210610556, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"33.1\", \"Scarcity (wt fraction/abundance)\": \"18350.0\", \"HHI (production)\": \"3029.0\", \"HHI (reserves)\": \"1870.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"66.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000107\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"16100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0038-1098(02)00555-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"132.0\", \"ZT\": \"0.1\", \"formula\": \"La0.45Ca2.55Co4O9\", \"comment\": \"\", \"synthesis\": \"sol-gel, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Nan 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"34.03\", \"Scarcity (wt fraction/abundance)\": \"18900.0\", \"HHI (production)\": \"3266.0\", \"HHI (reserves)\": \"1923.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"56.8\", \"Power Factor (W/(K\\u00b2m))\": \"9.86e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000814\", \"Seebeck coefficient (\\u03bcCV/K)\": \"70.0\", \"ZT\": \"0.6\", \"formula\": \"Cr1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #40697, 300K\", \"marker\": \"{'radius': 1.8029739394, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.192\", \"Average atomic mass (g/mol)\": \"58.82\", \"Scarcity (wt fraction/abundance)\": \"557400.0\", \"HHI (production)\": \"1985.0\", \"HHI (reserves)\": \"3955.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.41\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.608\", \"Atoms per unit cell\": \"15.3\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1230.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000601\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4890.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.939\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000962\", \"Seebeck coefficient (\\u03bcCV/K)\": \"57.0\", \"ZT\": \"0.34\", \"formula\": \"Mn1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #249898, 300K\", \"marker\": \"{'radius': 1.0303775522, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.882\", \"Average atomic mass (g/mol)\": \"59.07\", \"Scarcity (wt fraction/abundance)\": \"554800.0\", \"HHI (production)\": \"1871.0\", \"HHI (reserves)\": \"3777.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"816.76\", \"Average atomic volume (\\u212b\\u00b3)\": \"18.15\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1040.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000343\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"3300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.88\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000826\", \"Seebeck coefficient (\\u03bcCV/K)\": \"54.0\", \"ZT\": \"0.35\", \"formula\": \"Fe1.3Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #632653, 300K\", \"marker\": \"{'radius': 1.0561573095, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"3.416\", \"Average atomic mass (g/mol)\": \"59.14\", \"Scarcity (wt fraction/abundance)\": \"554000.0\", \"HHI (production)\": \"1937.0\", \"HHI (reserves)\": \"3740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"807.22\", \"Average atomic volume (\\u212b\\u00b3)\": \"17.938\", \"Atoms per unit cell\": \"45.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1210.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000352\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"2910.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.865\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.000468\", \"Seebeck coefficient (\\u03bcCV/K)\": \"33.0\", \"ZT\": \"0.24\", \"formula\": \"Ni2.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602930, 300K\", \"marker\": \"{'radius': 0.707217847, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"5.975\", \"Average atomic mass (g/mol)\": \"59.35\", \"Scarcity (wt fraction/abundance)\": \"528800.0\", \"HHI (production)\": \"1782.0\", \"HHI (reserves)\": \"3642.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"801.34\", \"Average atomic volume (\\u212b\\u00b3)\": \"16.695\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2140.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000236\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"1100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.872\"}, {\"doi\": \"10.1007/s11664-009-0975-0\", \"Electrical resistivity (\\u03a9cm)\": \"0.00218\", \"Seebeck coefficient (\\u03bcCV/K)\": \"133.0\", \"ZT\": \"0.81\", \"formula\": \"Cu4.0Mo6S8\", \"comment\": \"\", \"synthesis\": \"solid state reaction, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohta 2010\", \"Structure\": \"ICSD #602374, 300K\", \"marker\": \"{'radius': 2.435294497, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.039\", \"Average atomic mass (g/mol)\": \"60.36\", \"Scarcity (wt fraction/abundance)\": \"465000.0\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"3380.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"853.58\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.807\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"459.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000812\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"17700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.549\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00519\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-96.0\", \"ZT\": \"0.18\", \"formula\": \"Ca0.9Bi0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #98592, 300K\", \"marker\": \"{'radius': 0.5328640651, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"1.841\", \"Average atomic mass (g/mol)\": \"31.98\", \"Scarcity (wt fraction/abundance)\": \"7688000.0\", \"HHI (production)\": \"2260.0\", \"HHI (reserves)\": \"1887.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"213.57\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.678\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"193.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000178\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"9220.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.255\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00789\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-80.0\", \"ZT\": \"0.08\", \"formula\": \"Ca0.9Ce0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.6\", \"Scarcity (wt fraction/abundance)\": \"1819.0\", \"HHI (production)\": \"2506.0\", \"HHI (reserves)\": \"1440.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"127.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.21e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6480.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-108.0\", \"ZT\": \"0.07\", \"formula\": \"Ca0.9Y0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #246406, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"29.58\", \"Scarcity (wt fraction/abundance)\": \"2323.0\", \"HHI (production)\": \"2287.0\", \"HHI (reserves)\": \"1352.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"215.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.757\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"56.8\", \"Power Factor (W/(K\\u00b2m))\": \"6.57e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"11600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.00783\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-123.0\", \"ZT\": \"0.19\", \"formula\": \"Ca0.9Sm0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.5765629446, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.81\", \"Scarcity (wt fraction/abundance)\": \"15330.0\", \"HHI (production)\": \"2553.0\", \"HHI (reserves)\": \"1451.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"128.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000192\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.064\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-70.0\", \"ZT\": \"0.00765\", \"formula\": \"Ca0.9Sb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164748, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.24\", \"Scarcity (wt fraction/abundance)\": \"403100.0\", \"HHI (production)\": \"2295.0\", \"HHI (reserves)\": \"1442.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"210.39\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.519\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"15.6\", \"Power Factor (W/(K\\u00b2m))\": \"7.65e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4920.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.01\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-88.0\", \"ZT\": \"0.08\", \"formula\": \"Ca0.9La0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.58\", \"Scarcity (wt fraction/abundance)\": \"2861.0\", \"HHI (production)\": \"2501.0\", \"HHI (reserves)\": \"1438.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"97.2\", \"Power Factor (W/(K\\u00b2m))\": \"7.6e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7820.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.047\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-115.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9Pb0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.95\", \"Scarcity (wt fraction/abundance)\": \"11170.0\", \"HHI (production)\": \"1922.0\", \"HHI (reserves)\": \"1336.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.4\", \"Power Factor (W/(K\\u00b2m))\": \"2.81e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.173\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-235.0\", \"ZT\": \"0.03\", \"formula\": \"Ca0.9In0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.1\", \"Scarcity (wt fraction/abundance)\": \"372600.0\", \"HHI (production)\": \"1921.0\", \"HHI (reserves)\": \"1325.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"5.766\", \"Power Factor (W/(K\\u00b2m))\": \"3.18e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"55100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.479\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-145.0\", \"ZT\": \"0.00442\", \"formula\": \"Ca0.9Sn0.1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #164745, 293K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"30.18\", \"Scarcity (wt fraction/abundance)\": \"35350.0\", \"HHI (production)\": \"1866.0\", \"HHI (reserves)\": \"1298.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"212.03\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.602\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.089\", \"Power Factor (W/(K\\u00b2m))\": \"4.42e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"21200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1006/jssc.1995.1384\", \"Electrical resistivity (\\u03a9cm)\": \"0.087\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-193.0\", \"ZT\": \"0.04\", \"formula\": \"Ca1Mn1O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ohtaki 1995\", \"Structure\": \"ICSD #35218, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(179,16,12,.8)', 'fillColor': 'rgba(179,16,12,0)'}\", \"Thermal conductivity (W/mK)\": \"3.445\", \"Average atomic mass (g/mol)\": \"28.6\", \"Scarcity (wt fraction/abundance)\": \"398.0\", \"HHI (production)\": \"1861.0\", \"HHI (reserves)\": \"1276.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"206.97\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.348\", \"Atoms per unit cell\": \"20.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"11.4\", \"Power Factor (W/(K\\u00b2m))\": \"4.25e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"37200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.0081\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"1.664\", \"Seebeck coefficient (\\u03bcCV/K)\": \"617.0\", \"ZT\": \"0.02\", \"formula\": \"Cu1Cr1O2\", \"comment\": \"*res data at 300K/400K extrapolated from 600K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157800, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.708\", \"Average atomic mass (g/mol)\": \"36.88\", \"Scarcity (wt fraction/abundance)\": \"8516.0\", \"HHI (production)\": \"1881.0\", \"HHI (reserves)\": \"2193.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"0.601\", \"Power Factor (W/(K\\u00b2m))\": \"2.29e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"381000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.000395\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.366\", \"Seebeck coefficient (\\u03bcCV/K)\": \"446.0\", \"ZT\": \"0.05\", \"formula\": \"Cu1Cr0.99Mg0.01O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157801, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.948\", \"Average atomic mass (g/mol)\": \"36.82\", \"Scarcity (wt fraction/abundance)\": \"8514.0\", \"HHI (production)\": \"1882.0\", \"HHI (reserves)\": \"2184.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.922\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"2.732\", \"Power Factor (W/(K\\u00b2m))\": \"5.43e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"199000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00135\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.232\", \"Seebeck coefficient (\\u03bcCV/K)\": \"404.0\", \"ZT\": \"0.07\", \"formula\": \"Cu1Cr0.98Mg0.02O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157802, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.833\", \"Average atomic mass (g/mol)\": \"36.75\", \"Scarcity (wt fraction/abundance)\": \"8512.0\", \"HHI (production)\": \"1883.0\", \"HHI (reserves)\": \"2174.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.927\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"4.307\", \"Power Factor (W/(K\\u00b2m))\": \"7.02e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"163000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00217\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.047\", \"Seebeck coefficient (\\u03bcCV/K)\": \"325.0\", \"ZT\": \"0.22\", \"formula\": \"Cu1Cr0.97Mg0.03O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157803, 300K\", \"marker\": \"{'radius': 0.6749576981, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"4.776\", \"Average atomic mass (g/mol)\": \"36.68\", \"Scarcity (wt fraction/abundance)\": \"8511.0\", \"HHI (production)\": \"1885.0\", \"HHI (reserves)\": \"2165.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.14\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.928\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.000225\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"106000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.011\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.044\", \"Seebeck coefficient (\\u03bcCV/K)\": \"304.0\", \"ZT\": \"0.21\", \"formula\": \"Cu1Cr0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157804, 300K\", \"marker\": \"{'radius': 0.6254273127, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.854\", \"Average atomic mass (g/mol)\": \"36.61\", \"Scarcity (wt fraction/abundance)\": \"8509.0\", \"HHI (production)\": \"1886.0\", \"HHI (reserves)\": \"2156.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.2\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.933\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"22.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000208\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"92300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00804\"}, {\"doi\": \"10.1109/ICT.2006.331288\", \"Electrical resistivity (\\u03a9cm)\": \"0.041\", \"Seebeck coefficient (\\u03bcCV/K)\": \"325.0\", \"ZT\": \"0.26\", \"formula\": \"Cu1Cr0.95Mg0.05O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ono 2006\", \"Structure\": \"ICSD #157805, 300K\", \"marker\": \"{'radius': 0.778497513, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"6.988\", \"Average atomic mass (g/mol)\": \"36.54\", \"Scarcity (wt fraction/abundance)\": \"8507.0\", \"HHI (production)\": \"1887.0\", \"HHI (reserves)\": \"2146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"131.16\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.93\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"24.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000259\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"106000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00856\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.0006\", \"Seebeck coefficient (\\u03bcCV/K)\": \"200.0\", \"ZT\": \"6.67\", \"formula\": \"Na1Co2O4\", \"comment\": \"*values at 800 K\", \"synthesis\": \"flux (NaCl), air\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 20, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"4.764\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1670.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00667\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.854\"}, {\"doi\": \"10.1143/JJAP.40.4644\", \"Electrical resistivity (\\u03a9cm)\": \"0.004\", \"Seebeck coefficient (\\u03bcCV/K)\": \"175.0\", \"ZT\": \"0.77\", \"formula\": \"Na1Co2O4\", \"comment\": \"*values at 800 K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Fujita 2001\", \"Structure\": \"ICSD #21001, 300K\", \"marker\": \"{'radius': 2.296875, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.224\", \"Average atomic mass (g/mol)\": \"29.26\", \"Scarcity (wt fraction/abundance)\": \"20930.0\", \"HHI (production)\": \"2036.0\", \"HHI (reserves)\": \"1740.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"75.67\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.81\", \"Atoms per unit cell\": \"7.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"250.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000766\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.274\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.061\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-191.0\", \"ZT\": \"0.06\", \"formula\": \"Zn1O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.69\", \"Scarcity (wt fraction/abundance)\": \"10780.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1621.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"16.5\", \"Power Factor (W/(K\\u00b2m))\": \"6.02e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.025\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-182.0\", \"ZT\": \"0.13\", \"formula\": \"Zn0.98Al0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.39099939, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.31\", \"Scarcity (wt fraction/abundance)\": \"10670.0\", \"HHI (production)\": \"1361.0\", \"HHI (reserves)\": \"1612.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"39.3\", \"Power Factor (W/(K\\u00b2m))\": \"0.00013\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"33100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.019\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-174.0\", \"ZT\": \"0.16\", \"formula\": \"Zn0.97Al0.03O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.4663226144, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.11\", \"Scarcity (wt fraction/abundance)\": \"10610.0\", \"HHI (production)\": \"1360.0\", \"HHI (reserves)\": \"1608.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"51.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000155\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.018\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-164.0\", \"ZT\": \"0.15\", \"formula\": \"Zn0.95Al0.05O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.4428537821, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"39.73\", \"Scarcity (wt fraction/abundance)\": \"10490.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1599.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"54.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000148\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-217.0\", \"ZT\": \"0.27\", \"formula\": \"Zn0.97Al0.025Ti0.005O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.8140540693, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.17\", \"Scarcity (wt fraction/abundance)\": \"10600.0\", \"HHI (production)\": \"1359.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"57.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000271\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"47200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.016\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-212.0\", \"ZT\": \"0.28\", \"formula\": \"Zn0.97Al0.02Ti0.01O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.8501238198, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.22\", \"Scarcity (wt fraction/abundance)\": \"10580.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1609.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"62.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.000283\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"45100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.014\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-205.0\", \"ZT\": \"0.29\", \"formula\": \"Zn0.97Al0.015Ti0.015O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.8747676298, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.27\", \"Scarcity (wt fraction/abundance)\": \"10570.0\", \"HHI (production)\": \"1357.0\", \"HHI (reserves)\": \"1610.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"69.2\", \"Power Factor (W/(K\\u00b2m))\": \"0.000292\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/j.jeurceramsoc.2006.04.012\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-195.0\", \"ZT\": \"0.29\", \"formula\": \"Zn0.97Al0.01Ti0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Park 2007\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.8616186658, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"40.32\", \"Scarcity (wt fraction/abundance)\": \"10560.0\", \"HHI (production)\": \"1356.0\", \"HHI (reserves)\": \"1611.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"75.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000287\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00174\", \"Seebeck coefficient (\\u03bcCV/K)\": \"157.0\", \"ZT\": \"1.41\", \"formula\": \"Ce1Fe4Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #621065, 300K\", \"marker\": \"{'radius': 4.2273166672, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.33\", \"Scarcity (wt fraction/abundance)\": \"4005000.0\", \"HHI (production)\": \"7355.0\", \"HHI (reserves)\": \"3146.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"762.3\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.421\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"574.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00141\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"24600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.0023\", \"Seebeck coefficient (\\u03bcCV/K)\": \"176.0\", \"ZT\": \"1.35\", \"formula\": \"Ce1Fe3Co1Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 4.0540286423, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.51\", \"Scarcity (wt fraction/abundance)\": \"4000000.0\", \"HHI (production)\": \"7367.0\", \"HHI (reserves)\": \"3185.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"434.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00135\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00339\", \"Seebeck coefficient (\\u03bcCV/K)\": \"190.0\", \"ZT\": \"1.06\", \"formula\": \"Ce1Fe2.5Co1.5Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 3.1888705295, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.6\", \"Scarcity (wt fraction/abundance)\": \"3997000.0\", \"HHI (production)\": \"7373.0\", \"HHI (reserves)\": \"3204.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"756.81\", \"Average atomic volume (\\u212b\\u00b3)\": \"22.259\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"295.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00106\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00499\", \"Seebeck coefficient (\\u03bcCV/K)\": \"118.0\", \"ZT\": \"0.28\", \"formula\": \"Ce1Fe2Co2Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.833314218, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.69\", \"Scarcity (wt fraction/abundance)\": \"3994000.0\", \"HHI (production)\": \"7379.0\", \"HHI (reserves)\": \"3223.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"200.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000278\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00448\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-138.0\", \"ZT\": \"0.42\", \"formula\": \"Ce1Fe1Co3Sb12\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 1.2744357042, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.88\", \"Scarcity (wt fraction/abundance)\": \"3988000.0\", \"HHI (production)\": \"7391.0\", \"HHI (reserves)\": \"3261.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"223.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000425\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://www.jstor.org/stable/2889796\", \"Electrical resistivity (\\u03a9cm)\": \"0.00397\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-90.0\", \"ZT\": \"0.2\", \"formula\": \"Ce1Fe1.5Co2.5Sb12\", \"comment\": \"Unit Cell =Co1.26 Fe2.74 La0.743 Sb12\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sales 1996\", \"Structure\": \"ICSD #96163, 300K\", \"marker\": \"{'radius': 0.6101380995, 'lineColor': 'rgba(153,153,153,.8)', 'fillColor': 'rgba(153,153,153,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"107.78\", \"Scarcity (wt fraction/abundance)\": \"3991000.0\", \"HHI (production)\": \"7385.0\", \"HHI (reserves)\": \"3242.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"747.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.971\", \"Atoms per unit cell\": \"34.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"252.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000203\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"8080.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"http://orbit.dtu.dk/en/publications/improvement-of-niobium-doped-srtio3-by-nanostructuring(2b6f4b33-1a6f-4472-ac18-6996f91cd743).html\", \"Electrical resistivity (\\u03a9cm)\": \"0.00563\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-163.0\", \"ZT\": \"0.47\", \"formula\": \"Sr1Ti0.8Nb0.2O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Sonne 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 1.4187279289, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"2.555\", \"Average atomic mass (g/mol)\": \"38.5\", \"Scarcity (wt fraction/abundance)\": \"6498.0\", \"HHI (production)\": \"3072.0\", \"HHI (reserves)\": \"2648.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"178.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000473\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"26600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.17\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00833\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-192.0\", \"ZT\": \"0.44\", \"formula\": \"Sr1Dy0.08Ti0.92O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 1.32158016, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"2.97\", \"Average atomic mass (g/mol)\": \"38.53\", \"Scarcity (wt fraction/abundance)\": \"13120.0\", \"HHI (production)\": \"2920.0\", \"HHI (reserves)\": \"2055.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"120.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000441\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.099\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00418\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-142.0\", \"ZT\": \"0.48\", \"formula\": \"Sr1Nd0.17Ti0.83O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 1.441689108, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.397\", \"Average atomic mass (g/mol)\": \"39.97\", \"Scarcity (wt fraction/abundance)\": \"4528.0\", \"HHI (production)\": \"3337.0\", \"HHI (reserves)\": \"2128.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"239.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000481\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.172\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00395\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-140.0\", \"ZT\": \"0.5\", \"formula\": \"Sr1Nd0.2Ti0.8O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 1.48764, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.197\", \"Average atomic mass (g/mol)\": \"40.55\", \"Scarcity (wt fraction/abundance)\": \"5035.0\", \"HHI (production)\": \"3484.0\", \"HHI (reserves)\": \"2153.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"253.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000496\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"19600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.193\"}, {\"doi\": \"10.1007/978-3-540-88201-5_24\", \"Electrical resistivity (\\u03a9cm)\": \"0.00319\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-124.0\", \"ZT\": \"0.48\", \"formula\": \"Sr1Nd0.24Ti0.76O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tinh 2009\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 1.4438064, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.22\", \"Average atomic mass (g/mol)\": \"41.32\", \"Scarcity (wt fraction/abundance)\": \"5689.0\", \"HHI (production)\": \"3673.0\", \"HHI (reserves)\": \"2186.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"313.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000481\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"15400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.237\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"2.97\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-437.0\", \"ZT\": \"0.00643\", \"formula\": \"Zn1O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"8.58\", \"Average atomic mass (g/mol)\": \"40.69\", \"Scarcity (wt fraction/abundance)\": \"10780.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1621.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"21.0\", \"Power Factor (W/(K\\u00b2m))\": \"6.43e-06\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"191000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.00598\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00871\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-232.0\", \"ZT\": \"0.62\", \"formula\": \"Zn0.995Al0.005O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.846538245, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"8.25\", \"Average atomic mass (g/mol)\": \"40.59\", \"Scarcity (wt fraction/abundance)\": \"10760.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1619.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"99.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000616\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"53600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.029\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00457\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-167.0\", \"ZT\": \"0.61\", \"formula\": \"Zn0.99Al0.01O1\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 1.8330221536, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"8.25\", \"Average atomic mass (g/mol)\": \"40.5\", \"Scarcity (wt fraction/abundance)\": \"10730.0\", \"HHI (production)\": \"1362.0\", \"HHI (reserves)\": \"1616.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"186.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000611\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"27900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.055\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00182\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-175.0\", \"ZT\": \"1.68\", \"formula\": \"Zn0.98Al0.02O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 5.0489067786, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"7.92\", \"Average atomic mass (g/mol)\": \"40.31\", \"Scarcity (wt fraction/abundance)\": \"10670.0\", \"HHI (production)\": \"1361.0\", \"HHI (reserves)\": \"1612.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"444.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00168\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"30600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.137\"}, {\"doi\": \"10.1039/A602506D\", \"Electrical resistivity (\\u03a9cm)\": \"0.00282\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-200.0\", \"ZT\": \"1.42\", \"formula\": \"Zn0.95Al0.05O1\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Tsubota 1997\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 4.2588677605, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"6.23\", \"Average atomic mass (g/mol)\": \"39.73\", \"Scarcity (wt fraction/abundance)\": \"10490.0\", \"HHI (production)\": \"1358.0\", \"HHI (reserves)\": \"1599.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"332.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00142\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.13\"}, {\"doi\": \"10.1016/j.jallcom.2010.06.195\", \"Electrical resistivity (\\u03a9cm)\": \"0.024\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-177.0\", \"ZT\": \"0.13\", \"formula\": \"Sr1Nb0.15Ti0.85O3\", \"comment\": \"*Values at 1000K extrapolated from 900K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Wang 2010\", \"Structure\": \"ICSD #174464, 293K\", \"marker\": \"{'radius': 0.3834591124, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"3.078\", \"Average atomic mass (g/mol)\": \"38.05\", \"Scarcity (wt fraction/abundance)\": \"5257.0\", \"HHI (production)\": \"2915.0\", \"HHI (reserves)\": \"2484.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"60.64\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.128\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"40.9\", \"Power Factor (W/(K\\u00b2m))\": \"0.000128\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.032\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.00171\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-142.0\", \"ZT\": \"1.18\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"Czochralski method, He\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 3.5365474386, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.6\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"585.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00118\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.892\"}, {\"doi\": \"10.1103/PhysRevB.77.075203\", \"Electrical resistivity (\\u03a9cm)\": \"0.00223\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-144.0\", \"ZT\": \"0.94\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Toberer 2008\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 2.8051156951, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.26\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"448.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000935\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"20900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.868\"}, {\"doi\": \"10.1063/1.2163979\", \"Electrical resistivity (\\u03a9cm)\": \"0.002\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-200.0\", \"ZT\": \"2.0\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"*resistivity extrapolated from 900K\", \"synthesis\": \"Czochralski method, argon\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Saramat 2006\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 6.0120240481, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.43\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"501.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.002\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.855\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.00186\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-212.0\", \"ZT\": \"2.43\", \"formula\": \"Mg2Si0.98Bi0.02\", \"comment\": \"*value at 940 K\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 7.2813069467, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.75\", \"Average atomic mass (g/mol)\": \"26.77\", \"Scarcity (wt fraction/abundance)\": \"3061000.0\", \"HHI (production)\": \"5072.0\", \"HHI (reserves)\": \"957.2\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"539.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00243\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"45100.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.478\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.0022\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-188.0\", \"ZT\": \"1.6\", \"formula\": \"Mg2Si0.6Ge0.4Bi0.02\", \"comment\": \"*value at 940 K\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 4.8042668182, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.73\", \"Average atomic mass (g/mol)\": \"32.68\", \"Scarcity (wt fraction/abundance)\": \"2694000.0\", \"HHI (production)\": \"5169.0\", \"HHI (reserves)\": \"1229.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"455.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0016\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"35200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.641\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.0066\", \"Seebeck coefficient (\\u03bcCV/K)\": \"192.0\", \"ZT\": \"0.56\", \"formula\": \"Mg2Si0.98Ag0.02\", \"comment\": \"*value at 930 K\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #163708, 300K\", \"marker\": \"{'radius': 1.6756363636, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.16\", \"Average atomic mass (g/mol)\": \"26.1\", \"Scarcity (wt fraction/abundance)\": \"353300.0\", \"HHI (production)\": \"4954.0\", \"HHI (reserves)\": \"699.7\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.55\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.546\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"152.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000559\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"36900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.117\"}, {\"doi\": \"10.1007/s11664-009-0735-1\", \"Electrical resistivity (\\u03a9cm)\": \"0.00544\", \"Seebeck coefficient (\\u03bcCV/K)\": \"224.0\", \"ZT\": \"0.92\", \"formula\": \"Mg2Si0.6Ge0.4Ag0.02\", \"comment\": \"*value at 926 K\", \"synthesis\": \"solid state reaction, He/H2\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Mars 2009\", \"Structure\": \"ICSD #180947, 300K\", \"marker\": \"{'radius': 2.7670588235, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.48\", \"Average atomic mass (g/mol)\": \"32.01\", \"Scarcity (wt fraction/abundance)\": \"493400.0\", \"HHI (production)\": \"5075.0\", \"HHI (reserves)\": \"1026.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"258.35\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.529\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"184.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000922\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"50200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.129\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00625\", \"Seebeck coefficient (\\u03bcCV/K)\": \"289.0\", \"ZT\": \"1.34\", \"formula\": \"Ba8Ga16Ge30\", \"comment\": \"*value at 920 K, kappa extrapolated\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 4.009008, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.0\", \"Average atomic mass (g/mol)\": \"81.36\", \"Scarcity (wt fraction/abundance)\": \"356000.0\", \"HHI (production)\": \"4753.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"160.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00134\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"83500.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.195\"}, {\"doi\": \"10.1109/ICT.2002.1190269\", \"Electrical resistivity (\\u03a9cm)\": \"0.00735\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-266.0\", \"ZT\": \"0.96\", \"formula\": \"Ba8Ga18Ge28\", \"comment\": \"*value at 920 K\", \"synthesis\": \"arc melting\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Anno 2002\", \"Structure\": \"ICSD #94298, 300K\", \"marker\": \"{'radius': 2.888, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"1.0\", \"Average atomic mass (g/mol)\": \"81.25\", \"Scarcity (wt fraction/abundance)\": \"335300.0\", \"HHI (production)\": \"4759.0\", \"HHI (reserves)\": \"2008.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1254.12\", \"Average atomic volume (\\u212b\\u00b3)\": \"23.224\", \"Atoms per unit cell\": \"54.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"136.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000963\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"70800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.332\"}, {\"doi\": \"10.1038/nmat3276\", \"Electrical resistivity (\\u03a9cm)\": \"0.0078\", \"Seebeck coefficient (\\u03bcCV/K)\": \"297.0\", \"ZT\": \"1.13\", \"formula\": \"Cu2Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 3.3926538462, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.745\", \"Average atomic mass (g/mol)\": \"68.68\", \"Scarcity (wt fraction/abundance)\": \"7674000.0\", \"HHI (production)\": \"1825.0\", \"HHI (reserves)\": \"1672.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"128.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00113\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"88200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.42\"}, {\"doi\": \"10.1038/nmat3280\", \"Electrical resistivity (\\u03a9cm)\": \"0.00325\", \"Seebeck coefficient (\\u03bcCV/K)\": \"202.0\", \"ZT\": \"1.25\", \"formula\": \"Cu1.98Se1\", \"comment\": \"\", \"synthesis\": \"melted, vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Liu 2012\", \"Structure\": \"ICSD #41140, 293K\", \"marker\": \"{'radius': 3.7479, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.015\", \"Average atomic mass (g/mol)\": \"68.72\", \"Scarcity (wt fraction/abundance)\": \"7721000.0\", \"HHI (production)\": \"1826.0\", \"HHI (reserves)\": \"1673.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"184.61\", \"Average atomic volume (\\u212b\\u00b3)\": \"15.384\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"308.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00125\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"40600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.74\"}, {\"doi\": \"http://link.aip.org/link/doi/10.1063/1.1562337\", \"Electrical resistivity (\\u03a9cm)\": \"0.00227\", \"Seebeck coefficient (\\u03bcCV/K)\": \"245.0\", \"ZT\": \"2.64\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"flux (SrCl2), air\", \"form\": \"single crystal\", \"temperature\": \"1000\", \"author\": \"Shikano 2003\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 7.929326288, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.837\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"440.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00264\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"60000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.379\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00897\", \"Seebeck coefficient (\\u03bcCV/K)\": \"177.0\", \"ZT\": \"0.35\", \"formula\": \"Ca3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 1.0480263158, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.75\", \"Average atomic mass (g/mol)\": \"31.25\", \"Scarcity (wt fraction/abundance)\": \"17150.0\", \"HHI (production)\": \"2511.0\", \"HHI (reserves)\": \"1757.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"112.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000349\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"31300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.155\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00728\", \"Seebeck coefficient (\\u03bcCV/K)\": \"184.0\", \"ZT\": \"0.46\", \"formula\": \"Ca2.7Na0.3Co4O9\", \"comment\": \"*kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 1.3945901414, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.05\", \"Average atomic mass (g/mol)\": \"30.93\", \"Scarcity (wt fraction/abundance)\": \"17330.0\", \"HHI (production)\": \"2459.0\", \"HHI (reserves)\": \"1745.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"137.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000465\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"33900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.163\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00783\", \"Seebeck coefficient (\\u03bcCV/K)\": \"197.0\", \"ZT\": \"0.49\", \"formula\": \"Ca2.7Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 1.4837277487, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"2.05\", \"Average atomic mass (g/mol)\": \"34.41\", \"Scarcity (wt fraction/abundance)\": \"6713000.0\", \"HHI (production)\": \"2799.0\", \"HHI (reserves)\": \"2245.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"128.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000495\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"38700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.152\"}, {\"doi\": \"10.1063/1.1480115\", \"Electrical resistivity (\\u03a9cm)\": \"0.00762\", \"Seebeck coefficient (\\u03bcCV/K)\": \"205.0\", \"ZT\": \"0.55\", \"formula\": \"Ca2.4Na0.3Bi0.3Co4O9\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Xu 2002\", \"Structure\": \"ICSD #160556, 300K\", \"marker\": \"{'radius': 1.6540934138, 'lineColor': 'rgba(230,158,26,.8)', 'fillColor': 'rgba(230,158,26,0)'}\", \"Thermal conductivity (W/mK)\": \"1.75\", \"Average atomic mass (g/mol)\": \"34.09\", \"Scarcity (wt fraction/abundance)\": \"6776000.0\", \"HHI (production)\": \"2754.0\", \"HHI (reserves)\": \"2239.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"147.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.865\", \"Atoms per unit cell\": \"13.54\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"131.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000551\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.183\"}, {\"doi\": \"http://jjap.jsap.jp/link?JJAP/43/L540/\", \"Electrical resistivity (\\u03a9cm)\": \"0.00661\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-228.0\", \"ZT\": \"0.79\", \"formula\": \"Sr0.9Y0.1Ti1O3\", \"comment\": \"*extrapolated from 937 K, kappa estimated\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Obara 2004\", \"Structure\": \"ICSD #181231, 300K\", \"marker\": \"{'radius': 2.357907469, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"4.5\", \"Average atomic mass (g/mol)\": \"36.72\", \"Scarcity (wt fraction/abundance)\": \"2782.0\", \"HHI (production)\": \"2693.0\", \"HHI (reserves)\": \"1952.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"59.36\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.872\", \"Atoms per unit cell\": \"5.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"151.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000786\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"52000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.082\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.107\", \"Seebeck coefficient (\\u03bcCV/K)\": \"317.0\", \"ZT\": \"0.09\", \"formula\": \"Cu1Rh1O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.61\", \"Scarcity (wt fraction/abundance)\": \"518600000.0\", \"HHI (production)\": \"2265.0\", \"HHI (reserves)\": \"4717.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"9.381\", \"Power Factor (W/(K\\u00b2m))\": \"9.43e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"100000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.049\", \"Seebeck coefficient (\\u03bcCV/K)\": \"315.0\", \"ZT\": \"0.2\", \"formula\": \"Cu1Rh0.99Mg0.01O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 0.6099897541, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"49.42\", \"Scarcity (wt fraction/abundance)\": \"515400000.0\", \"HHI (production)\": \"2263.0\", \"HHI (reserves)\": \"4695.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"20.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000203\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"99200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"271.0\", \"ZT\": \"0.43\", \"formula\": \"Cu1Rh0.96Mg0.04O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 1.2884385965, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"48.83\", \"Scarcity (wt fraction/abundance)\": \"505800000.0\", \"HHI (production)\": \"2259.0\", \"HHI (reserves)\": \"4627.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"58.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000429\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"73400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1103/PhysRevB.80.115103\", \"Electrical resistivity (\\u03a9cm)\": \"0.00408\", \"Seebeck coefficient (\\u03bcCV/K)\": \"168.0\", \"ZT\": \"0.69\", \"formula\": \"Cu1Rh0.6Mg0.4O2\", \"comment\": \"\", \"synthesis\": \"solid state reaction , air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Maignan 2009\", \"Structure\": \"ICSD #29214, 300K\", \"marker\": \"{'radius': 2.0802382353, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"41.75\", \"Scarcity (wt fraction/abundance)\": \"369700000.0\", \"HHI (production)\": \"2199.0\", \"HHI (reserves)\": \"3662.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"140.56\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.713\", \"Atoms per unit cell\": \"12.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"245.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000693\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"28300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.113\", \"Seebeck coefficient (\\u03bcCV/K)\": \"265.0\", \"ZT\": \"0.06\", \"formula\": \"Ca3Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.692\", \"Average atomic mass (g/mol)\": \"73.21\", \"Scarcity (wt fraction/abundance)\": \"3564000.0\", \"HHI (production)\": \"6623.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"8.873\", \"Power Factor (W/(K\\u00b2m))\": \"6.25e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"70400.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.031\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.017\", \"Seebeck coefficient (\\u03bcCV/K)\": \"288.0\", \"ZT\": \"0.48\", \"formula\": \"Ca2.97Na0.03Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 1.4416787791, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.67\", \"Average atomic mass (g/mol)\": \"73.14\", \"Scarcity (wt fraction/abundance)\": \"3567000.0\", \"HHI (production)\": \"6622.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"58.1\", \"Power Factor (W/(K\\u00b2m))\": \"0.000481\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"82700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.212\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.013\", \"Seebeck coefficient (\\u03bcCV/K)\": \"262.0\", \"ZT\": \"0.51\", \"formula\": \"Ca2.94Na0.06Al1Sb3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 1.5368059701, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.698\", \"Average atomic mass (g/mol)\": \"73.07\", \"Scarcity (wt fraction/abundance)\": \"3571000.0\", \"HHI (production)\": \"6621.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"74.6\", \"Power Factor (W/(K\\u00b2m))\": \"0.000512\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"68600.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.261\"}, {\"doi\": \"10.1039/c0ee00517g\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"243.0\", \"ZT\": \"0.47\", \"formula\": \"Ca2.85Na0.15Al1Sb3\", \"comment\": \"*seebeck, kappa  extrapolated from800K\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Zevalkink 2011\", \"Structure\": \"ICSD #36363, 300K\", \"marker\": \"{'radius': 1.417176, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.68\", \"Average atomic mass (g/mol)\": \"72.85\", \"Scarcity (wt fraction/abundance)\": \"3582000.0\", \"HHI (production)\": \"6618.0\", \"HHI (reserves)\": \"2841.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"822.88\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.389\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"80.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000472\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"59000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.287\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.00605\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-87.0\", \"ZT\": \"0.13\", \"formula\": \"Fe0.998Co0.002Si2\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.3779152066, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"5.02\", \"Average atomic mass (g/mol)\": \"37.34\", \"Scarcity (wt fraction/abundance)\": \"48.87\", \"HHI (production)\": \"3570.0\", \"HHI (reserves)\": \"1187.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"165.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000126\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.08\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-101.0\", \"ZT\": \"0.08\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.04O0.06\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"4.21\", \"Average atomic mass (g/mol)\": \"37.6\", \"Scarcity (wt fraction/abundance)\": \"1051.0\", \"HHI (production)\": \"3739.0\", \"HHI (reserves)\": \"1227.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"82.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.33e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"10200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.048\"}, {\"doi\": \"10.1016/j.jallcom.2005.04.060\", \"Electrical resistivity (\\u03a9cm)\": \"0.021\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-68.0\", \"ZT\": \"0.02\", \"formula\": \"Fe0.978Co0.00196Si1.96Y0.12O0.18\", \"comment\": \"\", \"synthesis\": \"arc-melted, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Ito 2006\", \"Structure\": \"ICSD #9119, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(170,204,0,.8)', 'fillColor': 'rgba(170,204,0,0)'}\", \"Thermal conductivity (W/mK)\": \"3.22\", \"Average atomic mass (g/mol)\": \"38.06\", \"Scarcity (wt fraction/abundance)\": \"2834.0\", \"HHI (production)\": \"4040.0\", \"HHI (reserves)\": \"1297.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"601.91\", \"Average atomic volume (\\u212b\\u00b3)\": \"12.54\", \"Atoms per unit cell\": \"48.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"46.7\", \"Power Factor (W/(K\\u00b2m))\": \"2.16e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4620.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.035\"}, {\"doi\": \"10.1002/adfm.201000970\", \"Electrical resistivity (\\u03a9cm)\": \"0.00939\", \"Seebeck coefficient (\\u03bcCV/K)\": \"207.0\", \"ZT\": \"0.46\", \"formula\": \"Ca4.75Na0.25Al2Sb6\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Toberer 2010\", \"Structure\": \"ICSD #183853, 300K\", \"marker\": \"{'radius': 1.3689776358, 'lineColor': 'rgba(255,80,0,.8)', 'fillColor': 'rgba(255,80,0,0)'}\", \"Thermal conductivity (W/mK)\": \"0.703\", \"Average atomic mass (g/mol)\": \"75.43\", \"Scarcity (wt fraction/abundance)\": \"3725000.0\", \"HHI (production)\": \"6732.0\", \"HHI (reserves)\": \"2896.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"770.68\", \"Average atomic volume (\\u212b\\u00b3)\": \"29.642\", \"Atoms per unit cell\": \"26.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"106.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000456\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"42800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.37\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.138\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-372.0\", \"ZT\": \"0.1\", \"formula\": \"Fe1.98Ti0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.300382958, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"31.91\", \"Scarcity (wt fraction/abundance)\": \"13.87\", \"HHI (production)\": \"1837.0\", \"HHI (reserves)\": \"1111.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"72400.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.0001\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"138000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.072\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-328.0\", \"ZT\": \"0.15\", \"formula\": \"Fe1.96Ti0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.4486797085, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.54\", \"Average atomic mass (g/mol)\": \"31.87\", \"Scarcity (wt fraction/abundance)\": \"14.74\", \"HHI (production)\": \"1829.0\", \"HHI (reserves)\": \"1112.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"139000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00015\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"108000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"95.6\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.058\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-295.0\", \"ZT\": \"0.15\", \"formula\": \"Fe1.94Ti0.06O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #168009, 293K\", \"marker\": \"{'radius': 0.4526723323, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.35\", \"Average atomic mass (g/mol)\": \"31.84\", \"Scarcity (wt fraction/abundance)\": \"15.62\", \"HHI (production)\": \"1820.0\", \"HHI (reserves)\": \"1113.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"101.11\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.111\", \"Atoms per unit cell\": \"10.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"174000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000151\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"86900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"127.0\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.162\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-375.0\", \"ZT\": \"0.09\", \"formula\": \"Fe1.98Sn0.02O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"\", \"Average atomic mass (g/mol)\": \"32.19\", \"Scarcity (wt fraction/abundance)\": \"6569.0\", \"HHI (production)\": \"1853.0\", \"HHI (reserves)\": \"1117.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"61600.0\", \"Power Factor (W/(K\\u00b2m))\": \"8.64e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"140000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"\"}, {\"doi\": \"10.1016/S0925-8388(01)01804-7\", \"Electrical resistivity (\\u03a9cm)\": \"0.087\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-323.0\", \"ZT\": \"0.12\", \"formula\": \"Fe1.96Sn0.04O3\", \"comment\": \"\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Muta 2002\", \"Structure\": \"ICSD #84729, 300K\", \"marker\": \"{'radius': 0.359595085, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.08\", \"Average atomic mass (g/mol)\": \"32.44\", \"Scarcity (wt fraction/abundance)\": \"13020.0\", \"HHI (production)\": \"1860.0\", \"HHI (reserves)\": \"1122.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"303.23\", \"Average atomic volume (\\u212b\\u00b3)\": \"10.108\", \"Atoms per unit cell\": \"30.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"115000.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00012\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"105000.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"90.8\"}, {\"doi\": \"10.1016/j.jssc.2011.02.027\", \"Electrical resistivity (\\u03a9cm)\": \"0.00112\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-79.0\", \"ZT\": \"0.56\", \"formula\": \"Ba7Sr1Al16Si30\", \"comment\": \"\", \"synthesis\": \"flux (Al), dynamic vacuum\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Roudebush 2011\", \"Structure\": \"ICSD #380509, 90K\", \"marker\": \"{'radius': 1.6776627391, 'lineColor': 'rgba(156,83,0,.8)', 'fillColor': 'rgba(156,83,0,0)'}\", \"Thermal conductivity (W/mK)\": \"2.57\", \"Average atomic mass (g/mol)\": \"43.02\", \"Scarcity (wt fraction/abundance)\": \"1088.0\", \"HHI (production)\": \"3387.0\", \"HHI (reserves)\": \"1633.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"1193.0\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.691\", \"Atoms per unit cell\": \"55.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"895.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000559\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6250.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.85\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.00158\", \"Seebeck coefficient (\\u03bcCV/K)\": \"26.0\", \"ZT\": \"0.04\", \"formula\": \"Nd2Cu1O4\", \"comment\": \"*Seebeck extrapolated from 700K, kappa extrapolated from 850 K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.94\", \"Average atomic mass (g/mol)\": \"59.43\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6889.0\", \"HHI (reserves)\": \"2479.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"631.0\", \"Power Factor (W/(K\\u00b2m))\": \"4.35e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"690.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.391\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.023\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-83.0\", \"ZT\": \"0.03\", \"formula\": \"Nd2Cu0.98Ni0.02O4\", \"comment\": \"*Seebeck extrapolated from 700K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.902\", \"Average atomic mass (g/mol)\": \"59.42\", \"Scarcity (wt fraction/abundance)\": \"20980.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2480.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"43.6\", \"Power Factor (W/(K\\u00b2m))\": \"2.98e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"6830.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.027\"}, {\"doi\": \"10.1002/chin.200318015\", \"Electrical resistivity (\\u03a9cm)\": \"0.037\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-64.0\", \"ZT\": \"0.01\", \"formula\": \"Nd2Cu0.98Zn0.02O4\", \"comment\": \"*Seebeck extrapolated from 700K\", \"synthesis\": \"solid state reaction, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Kurosaki 2003\", \"Structure\": \"ICSD #261375, 298K\", \"marker\": \"{'radius': 0.9, 'lineColor': 'rgba(26,191,191,.8)', 'fillColor': 'rgba(26,191,191,0)'}\", \"Thermal conductivity (W/mK)\": \"3.63\", \"Average atomic mass (g/mol)\": \"59.44\", \"Scarcity (wt fraction/abundance)\": \"21000.0\", \"HHI (production)\": \"6888.0\", \"HHI (reserves)\": \"2481.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"189.28\", \"Average atomic volume (\\u212b\\u00b3)\": \"13.52\", \"Atoms per unit cell\": \"14.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"26.9\", \"Power Factor (W/(K\\u00b2m))\": \"1.09e-05\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"4060.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.018\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00103\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-88.0\", \"ZT\": \"0.75\", \"formula\": \"La3Te3.8Sb0.2\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 2.2452932039, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.66\", \"Average atomic mass (g/mol)\": \"132.28\", \"Scarcity (wt fraction/abundance)\": \"523800000.0\", \"HHI (production)\": \"5987.0\", \"HHI (reserves)\": \"4082.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"971.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000748\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"7710.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.891\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00225\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-117.0\", \"ZT\": \"0.61\", \"formula\": \"La3Te3.65Sb0.35\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 1.834572, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.85\", \"Average atomic mass (g/mol)\": \"132.15\", \"Scarcity (wt fraction/abundance)\": \"503700000.0\", \"HHI (production)\": \"6089.0\", \"HHI (reserves)\": \"4051.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"444.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000612\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"13800.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.586\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00687\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-221.0\", \"ZT\": \"0.71\", \"formula\": \"La3Te3.35Sb0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 2.1366567686, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.987\", \"Average atomic mass (g/mol)\": \"131.9\", \"Scarcity (wt fraction/abundance)\": \"463400000.0\", \"HHI (production)\": \"6293.0\", \"HHI (reserves)\": \"3990.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"146.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000712\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"48900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.36\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00527\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-185.0\", \"ZT\": \"0.65\", \"formula\": \"La3Te3.35Bi0.65\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 1.9525070209, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"1.37\", \"Average atomic mass (g/mol)\": \"140.0\", \"Scarcity (wt fraction/abundance)\": \"444300000.0\", \"HHI (production)\": \"6025.0\", \"HHI (reserves)\": \"4313.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"190.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000651\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"34300.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.338\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.000974\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-75.0\", \"ZT\": \"0.57\", \"formula\": \"La2.99Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 1.7187135524, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"2.87\", \"Average atomic mass (g/mol)\": \"132.44\", \"Scarcity (wt fraction/abundance)\": \"551400000.0\", \"HHI (production)\": \"5846.0\", \"HHI (reserves)\": \"4124.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"1030.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000573\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"5580.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.873\"}, {\"doi\": \"10.1103/PhysRevB.81.125205\", \"Electrical resistivity (\\u03a9cm)\": \"0.00639\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-215.0\", \"ZT\": \"0.72\", \"formula\": \"La2.74Te4\", \"comment\": \"\", \"synthesis\": \"solid state reaction, Ar\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"May 2010\", \"Structure\": \"ICSD #642048, 300K\", \"marker\": \"{'radius': 2.1701877934, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.893\", \"Average atomic mass (g/mol)\": \"132.2\", \"Scarcity (wt fraction/abundance)\": \"572900000.0\", \"HHI (production)\": \"5704.0\", \"HHI (reserves)\": \"4163.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"893.06\", \"Average atomic volume (\\u212b\\u00b3)\": \"31.895\", \"Atoms per unit cell\": \"28.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"156.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.000723\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"46200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.428\"}, {\"doi\": \"10.1021/nl202439h\", \"Electrical resistivity (\\u03a9cm)\": \"0.012\", \"Seebeck coefficient (\\u03bcCV/K)\": \"-316.0\", \"ZT\": \"0.81\", \"formula\": \"Zn0.9975Al0.0025O1\", \"comment\": \"\", \"synthesis\": \"microwave solvothermal, air\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Jood 2011\", \"Structure\": \"ICSD #26170, 295K\", \"marker\": \"{'radius': 2.441179632, 'lineColor': 'rgba(3,63,140,.8)', 'fillColor': 'rgba(3,63,140,0)'}\", \"Thermal conductivity (W/mK)\": \"1.909\", \"Average atomic mass (g/mol)\": \"40.64\", \"Scarcity (wt fraction/abundance)\": \"10770.0\", \"HHI (production)\": \"1363.0\", \"HHI (reserves)\": \"1620.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"47.62\", \"Average atomic volume (\\u212b\\u00b3)\": \"11.905\", \"Atoms per unit cell\": \"4.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"81.5\", \"Power Factor (W/(K\\u00b2m))\": \"0.000814\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"99900.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.104\"}, {\"doi\": \"10.1021/nl8026795\", \"Electrical resistivity (\\u03a9cm)\": \"0.00248\", \"Seebeck coefficient (\\u03bcCV/K)\": \"232.0\", \"ZT\": \"2.16\", \"formula\": \"Si0.8Ge0.2\", \"comment\": \"\", \"synthesis\": \"ball milling, hot-pressed nanopowders\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Joshi 2008\", \"Structure\": \"ICSD #53910, 300K\", \"marker\": \"{'radius': 6.4801705126, 'lineColor': 'rgba(51,51,51,.8)', 'fillColor': 'rgba(51,51,51,0)'}\", \"Thermal conductivity (W/mK)\": \"2.555\", \"Average atomic mass (g/mol)\": \"37.0\", \"Scarcity (wt fraction/abundance)\": \"270800.0\", \"HHI (production)\": \"4928.0\", \"HHI (reserves)\": \"1351.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"169.78\", \"Average atomic volume (\\u212b\\u00b3)\": \"21.222\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"403.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00216\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"53700.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.384\"}, {\"doi\": \"10.1038/nature11439\", \"Electrical resistivity (\\u03a9cm)\": \"0.00315\", \"Seebeck coefficient (\\u03bcCV/K)\": \"265.0\", \"ZT\": \"2.23\", \"formula\": \"Pb0.96Sr0.4Te1Na0.2\", \"comment\": \"*data from 900K\", \"synthesis\": \"sparks plasma sintering\", \"form\": \"polycrystalline\", \"temperature\": \"1000\", \"author\": \"Biswas 2012\", \"Structure\": \"ICSD #63099, 298K\", \"marker\": \"{'radius': 6.6783975, 'lineColor': 'rgba(2,102,7,.8)', 'fillColor': 'rgba(2,102,7,0)'}\", \"Thermal conductivity (W/mK)\": \"0.98\", \"Average atomic mass (g/mol)\": \"143.03\", \"Scarcity (wt fraction/abundance)\": \"348500000.0\", \"HHI (production)\": \"2897.0\", \"HHI (reserves)\": \"2980.0\", \"Unit cell volume (\\u212b\\u00b3)\": \"269.84\", \"Average atomic volume (\\u212b\\u00b3)\": \"33.73\", \"Atoms per unit cell\": \"8.0\", \"Electrical conductivity (\\u03a9\\u207b\\u00b9 cm\\u207b\\u00b9)\": \"317.0\", \"Power Factor (W/(K\\u00b2m))\": \"0.00223\", \"S\\u00b2 (\\u03bcV/K)\\u00b2\": \"70200.0\", \"Electronic fraction of thermal conductivity (\\u03f0\\u2091/\\u03f0)\": \"0.789\"}]"
  },
  {
    "path": "dataset/Magnetic Materials Database/MMD.csv",
    "content": "Formula,Formula units per cell,Atomic sites per cell,Crystal system,Formation energy (eV/atom),Energy relative to convex hull (eV/atom),Structure search,Averaged magnetic moment (μB/atom),\"Magnetic polarization, Js</(T)\",Magnetic easy axis,Magnetic anisotropy constants:Ka-c,Magnetic anisotropy constants:Kb-c (MJ/m3),Magnetic anisotropy constants:Kb-a (MJ/m3),Magnetic anisotropy constants:Kd-a (MJ/m3),\"Curie temperature, TC(K)\",Methods,References\r\nFe2Si,4,12,tetragonal,-0.361,0.023,AGA search,0.69,0.75,ab plane,-0.13,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si2,2,10,tetragonal,-0.402,0.033,AGA search,0.42,0.46,c,0.21,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si2,4,20,monoclinic,-0.39,0.045,AGA search,0.47,0.5,c,0.25,0.17,-0.08,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si,8,32,orthorhombic,-0.279,0.041,AGA search,1.04,1.11,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe6Si,4,28,orthorhombic,-0.167,0.016,AGA search,1.55,1.63,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si2,8,40,monoclinic,-0.421,0.014,AGA search,0.41,0.45,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe7Si2,4,36,orthorhombic,-0.275,0.009,AGA search,1.32,1.4,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe4Si3,2,14,tetragonal,-0.392,0.064,AGA search,0.36,0.4,c,0.9,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFeSi,1,2,cubic,-0.484,0.027,AGA search,0,0,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe2Si,8,24,orthorhombic,-0.378,0.006,AGA search,0.69,0.75,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe2Si,4,12,tetragonal,-0.374,0.01,AGA search,0.71,0.77,c,0.09,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe2Si,8,24,monoclinic,-0.363,0.021,AGA search,0.68,0.74,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe2Si,4,12,monoclinic,-0.362,0.021,AGA search,0.66,0.72,b,-0.06,-0.08,-0.02,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si2,8,40,monoclinic,-0.421,0.014,AGA search,0.41,0.45,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe7Si2,4,36,orthorhombic,-0.276,0.009,AGA search,1.33,1.4,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe7Si,4,32,triclinic,-0.157,0.003,AGA search,1.82,1.88,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe8Si,4,36,triclinic,-0.134,0.008,AGA search,1.89,1.94,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFeSi,1,2,hexagonal,-0.334,0.177,AGA search,0.35,0.36,c,0.74,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFeSi,4,8,monoclinic,-0.42,0.092,AGA search,0,0,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe5Si4,4,36,monoclinic,-0.435,0.034,AGA search,0.25,0.28,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe7Si3,4,40,monoclinic,-0.329,0.029,AGA search,0.93,1,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe7Si3,4,40,monoclinic,-0.332,0.026,AGA search,0.9,0.97,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe7Si3,4,40,monoclinic,-0.34,0.018,AGA search,0.86,0.92,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si,4,16,cubic,-0.32,0,AGA search,1.24,1.32,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si,4,16,orthorhombic,-0.284,0.035,AGA search,1.17,1.24,a,-0.3,0.28,0.58,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe3Si,8,32,monoclinic,-0.285,0.035,AGA search,1.33,1.39,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe4Si,8,40,monoclinic,-0.23,0.026,AGA search,1.62,1.68,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe5Si,4,24,triclinic,-0.182,0.031,AGA search,1.73,1.79,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe5Si,4,24,monoclinic,-0.165,0.048,AGA search,1.74,1.79,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe5Si,4,24,monoclinic,-0.172,0.041,AGA search,1.71,1.77,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe6Si,4,28,triclinic,-0.163,0.02,AGA search,1.76,1.82,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe6Si,4,28,triclinic,-0.163,0.019,AGA search,1.8,1.85,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe6Si,4,28,monoclinic,-0.14,0.043,AGA search,1.75,1.81,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe7Si,4,32,triclinic,-0.149,0.011,AGA search,1.84,1.9,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nFe8Si,4,36,triclinic,-0.131,0.011,AGA search,1.86,1.92,.,.,.,.,.,.,DFT,https://doi.org/10.1063/1.5036992\r\nCoN,4,8,cubic,0.085,0.085,AGA search,0,0,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCoN,2,4,hexagonal,0.144,0.144,AGA search,0,0,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo2N,2,6,orthorhombic,0.064,0.064,AGA search,0,0,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo2N,4,12,orthorhombic,0.098,0.098,AGA search,0.34,0.4,a,-1.11,-0.14,0.96,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo2N,2,6,triclinic,0.113,0.113,AGA search,0.14,0.18,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo2N,2,6,triclinic,0.122,0.122,AGA search,0.18,0.23,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo2N,2,6,orthorhombic,0.147,0.147,AGA search,0.32,0.42,c,0.21,0.38,0.17,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo2N,2,6,orthorhombic,0.149,0.149,AGA search,0.52,0.65,b,0.03,-0.41,-0.43,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,6,24,trigonal,0.068,0.068,AGA search,0.67,0.81,c,0.86,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,2,8,hexagonal,0.069,0.069,AGA search,0.72,0.87,c,0.12,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,4,16,orthorhombic,0.097,0.097,AGA search,0.59,0.69,b,-0.89,-1.47,-0.58,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,4,16,orthorhombic,0.109,0.109,AGA search,1.01,1.19,b,-0.18,-1.78,-1.6,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,4,16,orthorhombic,0.109,0.109,AGA search,1.03,1.21,c,0.91,0.04,-0.87,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,4,16,monoclinic,0.124,0.124,AGA search,0.6,0.72,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,4,16,orthorhombic,0.127,0.127,AGA search,0.72,0.83,b,0.01,-0.75,-0.76,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo3N,2,8,orthorhombic,0.135,0.135,AGA search,0.8,0.97,c,0.45,2.19,1.74,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,2,10,monoclinic,0.068,0.068,AGA search,0.93,1.09,a,-1.22,-0.68,0.54,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,4,20,monoclinic,0.072,0.072,AGA search,0.9,1.06,b,0.09,-0.12,-0.22,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,2,10,orthorhombic,0.078,0.078,AGA search,0.96,1.12,b,-0.1,-0.28,-0.18,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,1,5,cubic,0.075,0.075,AGA search,1.26,1.43,<111>,.,.,.,0,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,2,10,orthorhombic,0.08,0.08,AGA search,0.97,1.14,b,0.1,-1.24,-1.34,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,4,20,tetragonal,0.079,0.079,AGA search,1.26,1.43,c,2.1,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,4,20,orthorhombic,0.079,0.079,AGA search,0.81,0.93,b,-0.01,-0.75,-0.74,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,2,10,tetragonal,0.088,0.088,AGA search,1.23,1.4,c,3.11,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo4N,2,10,orthorhombic,0.088,0.088,AGA search,1.06,1.23,b,-0.19,-0.44,-0.25,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo5N,2,12,tetragonal,0.063,0.063,AGA search,1.14,1.3,ab plane,-2.43,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo5N,4,24,orthorhombic,0.063,0.063,AGA search,1.25,1.41,b,0.04,-0.97,-1.01,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo5N,4,24,orthorhombic,0.063,0.063,AGA search,1.26,1.42,a,-0.51,-0.26,0.24,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo5N,4,24,monoclinic,0.069,0.069,AGA search,1.08,1.24,b,0.49,-0.06,-0.55,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo5N,4,24,monoclinic,0.071,0.071,AGA search,1.18,1.35,c,0.29,1.33,1.04,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo5N,4,24,orthorhombic,0.08,0.08,AGA search,1.17,1.34,c,0.04,0.62,0.57,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo5N,4,24,orthorhombic,0.082,0.082,AGA search,1.08,1.24,c,0.08,0.04,-0.04,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,2,14,monoclinic,0.062,0.062,AGA search,1.15,1.32,a,-0.24,0.68,0.92,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,2,14,tetragonal,0.062,0.062,AGA search,1.35,1.51,c,0.54,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,2,14,triclinic,0.065,0.065,AGA search,1.28,1.45,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,4,28,orthorhombic,0.066,0.066,AGA search,1.2,1.37,b,-0.36,-2.08,-1.72,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,4,28,orthorhombic,0.073,0.073,AGA search,1.22,1.38,b,-0.87,-0.9,-0.03,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,3,21,trigonal,0.078,0.078,AGA search,1.2,1.37,ab plane,-0.29,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,2,14,orthorhombic,0.081,0.081,AGA search,1.21,1.37,b,-0.06,-0.68,-0.62,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo6N,1,7,trigonal,0.082,0.082,AGA search,1.24,1.41,c,0.54,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo7N,2,16,triclinic,0.051,0.051,AGA search,1.19,1.36,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo7N,4,32,monoclinic,0.057,0.057,AGA search,1.19,1.35,c,0.15,0.79,0.63,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo7N,4,32,orthorhombic,0.057,0.057,AGA search,1.38,1.53,c,0.18,0.02,-0.16,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo7N,4,32,orthorhombic,0.058,0.058,AGA search,1.36,1.51,b,0.02,-0.38,-0.39,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo7N,4,32,orthorhombic,0.069,0.069,AGA search,1.28,1.44,c,0.11,0.61,0.51,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo8N,4,36,cubic,0.039,0.039,AGA search,1.29,1.45,a,.,.,.,0,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo8N,2,18,monoclinic,0.041,0.041,AGA search,1.23,1.39,a,-0.54,-0.36,0.17,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo8N,2,18,monoclinic,0.041,0.041,AGA search,1.35,1.51,b,0.02,-0.07,-0.09,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo8N,2,18,orthorhombic,0.043,0.043,AGA search,1.3,1.45,b,-0.98,-1.5,-0.52,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nCo8N,2,18,orthorhombic,0.044,0.044,AGA search,1.22,1.38,a,-0.19,-0.06,0.14,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nZrCo5,6,36,trigonal,-0.123,0.068,AGA search,1,0.94,c,1.31,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevMaterials.2.084410\r\nZrCo5,6,36,trigonal,-0.135,0.055,AGA search,1.05,0.96,c,0.07,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevMaterials.2.084410\r\nZrCo5,4,24,hexagonal,-0.128,0.063,AGA search,1.01,0.94,c,1.05,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevMaterials.2.084410\r\nZrCo5,4,24,hexagonal,-0.128,0.063,AGA search,1.01,0.94,c,1.24,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevMaterials.2.084410\r\nZrCo5,1,6,hexagonal,-0.131,0.06,AGA search,1.08,0.97,c,1.01,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevMaterials.2.084410\r\nFeCo5N2,2,16,monoclinic,0.04,0.073,AGA search,0.8,0.95,b,-0.29,-0.34,-0.05,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo5N2,2,16,orthorhombic,0.063,0.096,AGA search,1.06,1.25,c,0.63,1.35,0.71,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo5N2,2,16,orthorhombic,0.066,0.099,AGA search,1.07,1.26,c,0.68,-0.96,-1.64,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo2N,4,16,orthorhombic,0.016,0.083,AGA search,0.99,1.17,a,-1.63,-0.46,1.17,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo2N,4,16,monoclinic,0.018,0.084,AGA search,0.92,1.09,b,-0.83,-0.98,-0.15,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo2N,4,16,orthorhombic,0.04,0.107,AGA search,1.14,1.33,c,1.64,2.17,0.53,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co3N2,1,8,triclinic,-0.005,0.079,AGA search,1.06,1.25,.,.,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co3N2,2,16,orthorhombic,0.009,0.093,AGA search,1.2,1.4,c,2.16,2.02,-0.15,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co3N2,2,16,orthorhombic,0.012,0.096,AGA search,1.37,1.59,c,2.21,2.14,-0.08,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2CoN,4,16,monoclinic,-0.028,0.073,AGA search,1.28,1.5,a,-1.36,-1.3,0.06,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2CoN,4,16,orthorhombic,-0.009,0.092,AGA search,1.5,1.72,b,1.01,-1.8,-2.81,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2CoN,4,16,orthorhombic,-0.002,0.099,AGA search,1.4,1.62,c,2.02,2.02,0,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe5CoN2,2,16,monoclinic,-0.047,0.045,AGA search,1.42,1.65,a,-1.08,-0.48,0.6,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe5CoN2,2,16,orthorhombic,-0.015,0.077,AGA search,1.49,1.73,c,1.47,2.56,1.09,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe5CoN2,2,16,orthorhombic,-0.008,0.084,AGA search,1.55,1.77,a,-1.37,-0.3,1.07,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo7N2,1,10,tetragonal,0.035,0.062,AGA search,1.37,1.54,ab plane,-0.4,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo7N2,2,20,tetragonal,0.043,0.069,AGA search,1.37,1.55,c,1.62,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo3N,1,5,cubic,-0.004,0.049,AGA search,1.48,1.66,a,.,.,.,0,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo3N,4,20,tetragonal,0.011,0.064,AGA search,1.47,1.65,c,1.27,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co5N2,1,10,orthorhombic,-0.024,0.043,AGA search,1.55,1.73,a,-0.07,-0.07,0.01,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co5N2,2,20,tetragonal,-0.011,0.056,AGA search,1.55,1.73,c,0.94,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co5N2,2,20,tetragonal,0.002,0.068,AGA search,1.51,1.7,c,1.58,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co2N,1,5,tetragonal,-0.04,0.041,AGA search,1.6,1.78,ab plane,-0.31,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co2N,4,20,orthorhombic,-0.019,0.062,AGA search,1.58,1.77,c,0.92,0.85,-0.07,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe5Co3N2,1,10,orthorhombic,-0.038,0.056,AGA search,1.65,1.82,a,-0.62,-0.75,-0.13,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe5Co3N2,2,20,tetragonal,-0.025,0.069,AGA search,1.68,1.86,c,2.01,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3CoN,2,10,orthorhombic,-0.036,0.054,AGA search,1.76,1.92,c,0.23,-0.46,-0.68,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3CoN,4,20,tetragonal,-0.033,0.057,AGA search,1.73,1.91,c,0.96,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe7CoN2,1,10,tetragonal,-0.037,0.037,AGA search,1.87,2.01,c,0.85,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe7CoN2,2,20,tetragonal,-0.032,0.042,AGA search,1.83,2,c,0.88,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo4N,4,24,orthorhombic,0.014,0.058,AGA search,1.41,1.57,c,1.09,0.92,-0.17,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo4N,4,24,orthorhombic,0.025,0.07,AGA search,1.39,1.56,c,0.99,1.02,0.03,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo4N,2,12,tetragonal,0.028,0.072,AGA search,1.28,1.46,ab plane,-1.89,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co3N,4,24,orthorhombic,-0.012,0.055,AGA search,1.52,1.68,c,1.4,1.24,-0.16,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co3N,4,24,orthorhombic,-0.01,0.057,AGA search,1.52,1.68,c,1.31,1.47,0.15,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co3N,4,24,orthorhombic,-0.009,0.058,AGA search,1.51,1.67,c,1.39,1.89,0.49,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co3N,4,24,orthorhombic,-0.009,0.058,AGA search,1.53,1.68,c,1.18,1.48,0.3,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co3N,4,24,orthorhombic,-0.008,0.059,AGA search,1.51,1.67,c,1.39,1.67,0.28,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co2N,4,24,orthorhombic,-0.018,0.071,AGA search,1.57,1.74,c,0.9,1.09,0.18,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co2N,4,24,orthorhombic,-0.014,0.076,AGA search,1.61,1.78,c,1.65,1.48,-0.17,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co2N,4,24,orthorhombic,-0.014,0.076,AGA search,1.6,1.77,c,0.88,1.05,0.17,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe4CoN,4,24,orthorhombic,-0.018,0.06,AGA search,1.85,1.99,c,1.12,1.15,0.04,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe4CoN,2,12,orthorhombic,-0.014,0.064,AGA search,1.83,1.98,c,0.89,0.88,-0.01,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe4CoN,4,24,orthorhombic,-0.013,0.065,AGA search,1.83,1.97,c,1.47,1.4,-0.07,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo5N,2,14,tetragonal,0.015,0.053,AGA search,1.49,1.64,c,0.53,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo5N,2,14,tetragonal,0.022,0.06,AGA search,1.47,1.63,ab plane,-0.01,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFeCo5N,2,14,tetragonal,0.024,0.062,AGA search,1.46,1.61,ab plane,-0.43,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co4N,2,14,tetragonal,-0.017,0.041,AGA search,1.57,1.72,c,0.54,.,.,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe2Co4N,2,14,orthorhombic,-0.012,0.046,AGA search,1.56,1.71,c,0.9,0.97,0.07,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\nFe3Co3N,2,14,orthorhombic,-0.019,0.058,AGA search,1.59,1.74,c,0.7,0.71,0.01,.,.,DFT,https://doi.org/10.1103/PhysRevB.94.224424\r\n"
  },
  {
    "path": "dataset/Magnetic Materials Database/all_info.json",
    "content": "[{\"Materials ID\": \"MMD-722\", \"Formula\": \"Fe2Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"12\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/mmm\\u00a0[123]\", \"Formation energy (eV/atom)\": \"-0.361\", \"Energy relative to convex hull (eV/atom)\": \"0.023\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.69\", \"Magnetic polarization, Js</(T)\": \"0.75\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-0.13\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-723\", \"Formula\": \"Fe3Si2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/m\\u00a0[83]\", \"Formation energy (eV/atom)\": \"-0.402\", \"Energy relative to convex hull (eV/atom)\": \"0.033\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.42\", \"Magnetic polarization, Js</(T)\": \"0.46\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.21\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-724\", \"Formula\": \"Fe3Si2\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"P2_1/m\\u00a0[11]\", \"Formation energy (eV/atom)\": \"-0.390\", \"Energy relative to convex hull (eV/atom)\": \"0.045\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.47\", \"Magnetic polarization, Js</(T)\": \"0.50\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.25\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.17\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.08\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-725\", \"Formula\": \"Fe3Si\", \"Formula units_per cell\": \"8\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"-0.279\", \"Energy relative to convex hull (eV/atom)\": \"0.041\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.04\", \"Magnetic polarization, Js</(T)\": \"1.11\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-726\", \"Formula\": \"Fe6Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"28\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"-0.167\", \"Energy relative to convex hull (eV/atom)\": \"0.016\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.55\", \"Magnetic polarization, Js</(T)\": \"1.63\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-727\", \"Formula\": \"Fe3Si2\", \"Formula units_per cell\": \"8\", \"Atomic_sites per cell\": \"40\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"-0.421\", \"Energy relative to convex hull (eV/atom)\": \"0.014\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.41\", \"Magnetic polarization, Js</(T)\": \"0.45\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-728\", \"Formula\": \"Fe7Si2\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"-0.275\", \"Energy relative to convex hull (eV/atom)\": \"0.009\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.32\", \"Magnetic polarization, Js</(T)\": \"1.40\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-729\", \"Formula\": \"Fe4Si3\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/mmm\\u00a0[139]\", \"Formation energy (eV/atom)\": \"-0.392\", \"Energy relative to convex hull (eV/atom)\": \"0.064\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.36\", \"Magnetic polarization, Js</(T)\": \"0.40\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.90\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-730\", \"Formula\": \"FeSi\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"2\", \"Crystal system\": \"cubic\", \"Space group [Number]\": \"Pm-3m\\u00a0[221]\", \"Formation energy (eV/atom)\": \"-0.484\", \"Energy relative to convex hull (eV/atom)\": \"0.027\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.00\", \"Magnetic polarization, Js</(T)\": \"0.00\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-731\", \"Formula\": \"Fe2Si\", \"Formula units_per cell\": \"8\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"-0.378\", \"Energy relative to convex hull (eV/atom)\": \"0.006\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.69\", \"Magnetic polarization, Js</(T)\": \"0.75\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-732\", \"Formula\": \"Fe2Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"12\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/nmm\\u00a0[129]\", \"Formation energy (eV/atom)\": \"-0.374\", \"Energy relative to convex hull (eV/atom)\": \"0.010\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.71\", \"Magnetic polarization, Js</(T)\": \"0.77\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.09\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-733\", \"Formula\": \"Fe2Si\", \"Formula units_per cell\": \"8\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"-0.363\", \"Energy relative to convex hull (eV/atom)\": \"0.021\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.68\", \"Magnetic polarization, Js</(T)\": \"0.74\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-734\", \"Formula\": \"Fe2Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"12\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"P2/m\\u00a0[10]\", \"Formation energy (eV/atom)\": \"-0.362\", \"Energy relative to convex hull (eV/atom)\": \"0.021\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.66\", \"Magnetic polarization, Js</(T)\": \"0.72\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.06\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.08\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.02\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-735\", \"Formula\": \"Fe3Si2\", \"Formula units_per cell\": \"8\", \"Atomic_sites per cell\": \"40\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"-0.421\", \"Energy relative to convex hull (eV/atom)\": \"0.014\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.41\", \"Magnetic polarization, Js</(T)\": \"0.45\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-736\", \"Formula\": \"Fe7Si2\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"-0.276\", \"Energy relative to convex hull (eV/atom)\": \"0.009\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.33\", \"Magnetic polarization, Js</(T)\": \"1.40\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-737\", \"Formula\": \"Fe7Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P1\\u00a0[1]\", \"Formation energy (eV/atom)\": \"-0.157\", \"Energy relative to convex hull (eV/atom)\": \"0.003\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.82\", \"Magnetic polarization, Js</(T)\": \"1.88\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-738\", \"Formula\": \"Fe8Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P-1\\u00a0[2]\", \"Formation energy (eV/atom)\": \"-0.134\", \"Energy relative to convex hull (eV/atom)\": \"0.008\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.89\", \"Magnetic polarization, Js</(T)\": \"1.94\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-739\", \"Formula\": \"FeSi\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"2\", \"Crystal system\": \"hexagonal\", \"Space group [Number]\": \"P-6m2\\u00a0[187]\", \"Formation energy (eV/atom)\": \"-0.334\", \"Energy relative to convex hull (eV/atom)\": \"0.177\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.35\", \"Magnetic polarization, Js</(T)\": \"0.36\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.74\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-740\", \"Formula\": \"FeSi\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"8\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"-0.420\", \"Energy relative to convex hull (eV/atom)\": \"0.092\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.00\", \"Magnetic polarization, Js</(T)\": \"0.00\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-741\", \"Formula\": \"Fe5Si4\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"P2/m\\u00a0[10]\", \"Formation energy (eV/atom)\": \"-0.435\", \"Energy relative to convex hull (eV/atom)\": \"0.034\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.25\", \"Magnetic polarization, Js</(T)\": \"0.28\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-742\", \"Formula\": \"Fe7Si3\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"40\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"P2_1/m\\u00a0[11]\", \"Formation energy (eV/atom)\": \"-0.329\", \"Energy relative to convex hull (eV/atom)\": \"0.029\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.93\", \"Magnetic polarization, Js</(T)\": \"1.00\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-743\", \"Formula\": \"Fe7Si3\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"40\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"Pm\\u00a0[6]\", \"Formation energy (eV/atom)\": \"-0.332\", \"Energy relative to convex hull (eV/atom)\": \"0.026\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.90\", \"Magnetic polarization, Js</(T)\": \"0.97\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-744\", \"Formula\": \"Fe7Si3\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"40\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"P2/m\\u00a0[10]\", \"Formation energy (eV/atom)\": \"-0.340\", \"Energy relative to convex hull (eV/atom)\": \"0.018\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.86\", \"Magnetic polarization, Js</(T)\": \"0.92\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-745\", \"Formula\": \"Fe3Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"cubic\", \"Space group [Number]\": \"Fm-3m\\u00a0[225]\", \"Formation energy (eV/atom)\": \"-0.320\", \"Energy relative to convex hull (eV/atom)\": \"0.000\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.24\", \"Magnetic polarization, Js</(T)\": \"1.32\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-746\", \"Formula\": \"Fe3Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"-0.284\", \"Energy relative to convex hull (eV/atom)\": \"0.035\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.17\", \"Magnetic polarization, Js</(T)\": \"1.24\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-0.30\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.28\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.58\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-747\", \"Formula\": \"Fe3Si\", \"Formula units_per cell\": \"8\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"-0.285\", \"Energy relative to convex hull (eV/atom)\": \"0.035\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.33\", \"Magnetic polarization, Js</(T)\": \"1.39\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-748\", \"Formula\": \"Fe4Si\", \"Formula units_per cell\": \"8\", \"Atomic_sites per cell\": \"40\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"-0.230\", \"Energy relative to convex hull (eV/atom)\": \"0.026\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.62\", \"Magnetic polarization, Js</(T)\": \"1.68\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-749\", \"Formula\": \"Fe5Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P1\\u00a0[1]\", \"Formation energy (eV/atom)\": \"-0.182\", \"Energy relative to convex hull (eV/atom)\": \"0.031\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.73\", \"Magnetic polarization, Js</(T)\": \"1.79\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-750\", \"Formula\": \"Fe5Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"P2_1/m\\u00a0[11]\", \"Formation energy (eV/atom)\": \"-0.165\", \"Energy relative to convex hull (eV/atom)\": \"0.048\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.74\", \"Magnetic polarization, Js</(T)\": \"1.79\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-751\", \"Formula\": \"Fe5Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"-0.172\", \"Energy relative to convex hull (eV/atom)\": \"0.041\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.71\", \"Magnetic polarization, Js</(T)\": \"1.77\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-752\", \"Formula\": \"Fe6Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"28\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P-1\\u00a0[2]\", \"Formation energy (eV/atom)\": \"-0.163\", \"Energy relative to convex hull (eV/atom)\": \"0.020\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.76\", \"Magnetic polarization, Js</(T)\": \"1.82\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-753\", \"Formula\": \"Fe6Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"28\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P1\\u00a0[1]\", \"Formation energy (eV/atom)\": \"-0.163\", \"Energy relative to convex hull (eV/atom)\": \"0.019\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.80\", \"Magnetic polarization, Js</(T)\": \"1.85\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-754\", \"Formula\": \"Fe6Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"28\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"Pm\\u00a0[6]\", \"Formation energy (eV/atom)\": \"-0.140\", \"Energy relative to convex hull (eV/atom)\": \"0.043\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.75\", \"Magnetic polarization, Js</(T)\": \"1.81\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-755\", \"Formula\": \"Fe7Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P-1\\u00a0[2]\", \"Formation energy (eV/atom)\": \"-0.149\", \"Energy relative to convex hull (eV/atom)\": \"0.011\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.84\", \"Magnetic polarization, Js</(T)\": \"1.90\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-756\", \"Formula\": \"Fe8Si\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P1\\u00a0[1]\", \"Formation energy (eV/atom)\": \"-0.131\", \"Energy relative to convex hull (eV/atom)\": \"0.011\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.86\", \"Magnetic polarization, Js</(T)\": \"1.92\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1063/1.5036992\"}, {\"Materials ID\": \"MMD-101\", \"Formula\": \"CoN\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"8\", \"Crystal system\": \"cubic\", \"Space group [Number]\": \"F-43m\\u00a0[216]\", \"Formation energy (eV/atom)\": \"0.085\", \"Energy relative to convex hull (eV/atom)\": \"0.085\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.00\", \"Magnetic polarization, Js</(T)\": \"0.00\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-102\", \"Formula\": \"CoN\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"4\", \"Crystal system\": \"hexagonal\", \"Space group [Number]\": \"P6_3mc\\u00a0[186]\", \"Formation energy (eV/atom)\": \"0.144\", \"Energy relative to convex hull (eV/atom)\": \"0.144\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.00\", \"Magnetic polarization, Js</(T)\": \"0.00\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-103\", \"Formula\": \"Co2N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"6\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pnnm\\u00a0[58]\", \"Formation energy (eV/atom)\": \"0.064\", \"Energy relative to convex hull (eV/atom)\": \"0.064\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.00\", \"Magnetic polarization, Js</(T)\": \"0.00\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-104\", \"Formula\": \"Co2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"12\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.098\", \"Energy relative to convex hull (eV/atom)\": \"0.098\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.34\", \"Magnetic polarization, Js</(T)\": \"0.40\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-1.11\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.14\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.96\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-105\", \"Formula\": \"Co2N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"6\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P1\\u00a0[1]\", \"Formation energy (eV/atom)\": \"0.113\", \"Energy relative to convex hull (eV/atom)\": \"0.113\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.14\", \"Magnetic polarization, Js</(T)\": \"0.18\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-106\", \"Formula\": \"Co2N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"6\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P1\\u00a0[1]\", \"Formation energy (eV/atom)\": \"0.122\", \"Energy relative to convex hull (eV/atom)\": \"0.122\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.18\", \"Magnetic polarization, Js</(T)\": \"0.23\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-107\", \"Formula\": \"Co2N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"6\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmn2_1\\u00a0[31]\", \"Formation energy (eV/atom)\": \"0.147\", \"Energy relative to convex hull (eV/atom)\": \"0.147\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.32\", \"Magnetic polarization, Js</(T)\": \"0.42\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.21\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.38\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.17\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-108\", \"Formula\": \"Co2N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"6\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmma\\u00a0[51]\", \"Formation energy (eV/atom)\": \"0.149\", \"Energy relative to convex hull (eV/atom)\": \"0.149\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.52\", \"Magnetic polarization, Js</(T)\": \"0.65\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.03\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.41\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.43\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-109\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"6\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"trigonal\", \"Space group [Number]\": \"R-3c\\u00a0[167]\", \"Formation energy (eV/atom)\": \"0.068\", \"Energy relative to convex hull (eV/atom)\": \"0.068\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.67\", \"Magnetic polarization, Js</(T)\": \"0.81\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.86\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-110\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"8\", \"Crystal system\": \"hexagonal\", \"Space group [Number]\": \"P6_322\\u00a0[182]\", \"Formation energy (eV/atom)\": \"0.069\", \"Energy relative to convex hull (eV/atom)\": \"0.069\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.72\", \"Magnetic polarization, Js</(T)\": \"0.87\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.12\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-111\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.097\", \"Energy relative to convex hull (eV/atom)\": \"0.097\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.59\", \"Magnetic polarization, Js</(T)\": \"0.69\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.89\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-1.47\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.58\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-112\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.109\", \"Energy relative to convex hull (eV/atom)\": \"0.109\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.01\", \"Magnetic polarization, Js</(T)\": \"1.19\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.18\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-1.78\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-1.60\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-113\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"0.109\", \"Energy relative to convex hull (eV/atom)\": \"0.109\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.03\", \"Magnetic polarization, Js</(T)\": \"1.21\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.91\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.04\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.87\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-114\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"Cm\\u00a0[8]\", \"Formation energy (eV/atom)\": \"0.124\", \"Energy relative to convex hull (eV/atom)\": \"0.124\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.60\", \"Magnetic polarization, Js</(T)\": \"0.72\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-115\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.127\", \"Energy relative to convex hull (eV/atom)\": \"0.127\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.72\", \"Magnetic polarization, Js</(T)\": \"0.83\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.01\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.75\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.76\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-116\", \"Formula\": \"Co3N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"8\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Immm\\u00a0[71]\", \"Formation energy (eV/atom)\": \"0.135\", \"Energy relative to convex hull (eV/atom)\": \"0.135\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.80\", \"Magnetic polarization, Js</(T)\": \"0.97\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.45\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"2.19\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"1.74\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-117\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"P2_1/c\\u00a0[14]\", \"Formation energy (eV/atom)\": \"0.068\", \"Energy relative to convex hull (eV/atom)\": \"0.068\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.93\", \"Magnetic polarization, Js</(T)\": \"1.09\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-1.22\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.68\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.54\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-118\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2\\u00a0[5]\", \"Formation energy (eV/atom)\": \"0.072\", \"Energy relative to convex hull (eV/atom)\": \"0.072\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.90\", \"Magnetic polarization, Js</(T)\": \"1.06\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.09\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.12\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.22\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-119\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"P2_12_12\\u00a0[18]\", \"Formation energy (eV/atom)\": \"0.078\", \"Energy relative to convex hull (eV/atom)\": \"0.078\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.96\", \"Magnetic polarization, Js</(T)\": \"1.12\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.10\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.28\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.18\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-120\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"5\", \"Crystal system\": \"cubic\", \"Space group [Number]\": \"Pm-3m\\u00a0[221]\", \"Formation energy (eV/atom)\": \"0.075\", \"Energy relative to convex hull (eV/atom)\": \"0.075\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.26\", \"Magnetic polarization, Js</(T)\": \"1.43\", \"Magnetic easy axis\": \"<111>\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \"-0.00\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-121\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmna\\u00a0[53]\", \"Formation energy (eV/atom)\": \"0.080\", \"Energy relative to convex hull (eV/atom)\": \"0.080\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.97\", \"Magnetic polarization, Js</(T)\": \"1.14\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.10\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-1.24\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-1.34\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-122\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/mmm\\u00a0[139]\", \"Formation energy (eV/atom)\": \"0.079\", \"Energy relative to convex hull (eV/atom)\": \"0.079\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.26\", \"Magnetic polarization, Js</(T)\": \"1.43\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"2.10\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-123\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.079\", \"Energy relative to convex hull (eV/atom)\": \"0.079\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.81\", \"Magnetic polarization, Js</(T)\": \"0.93\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.01\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.75\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.74\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-124\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/mmm\\u00a0[139]\", \"Formation energy (eV/atom)\": \"0.088\", \"Energy relative to convex hull (eV/atom)\": \"0.088\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.23\", \"Magnetic polarization, Js</(T)\": \"1.40\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"3.11\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-125\", \"Formula\": \"Co4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmma\\u00a0[51]\", \"Formation energy (eV/atom)\": \"0.088\", \"Energy relative to convex hull (eV/atom)\": \"0.088\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.06\", \"Magnetic polarization, Js</(T)\": \"1.23\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.19\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.44\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.25\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-126\", \"Formula\": \"Co5N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"12\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/m\\u00a0[87]\", \"Formation energy (eV/atom)\": \"0.063\", \"Energy relative to convex hull (eV/atom)\": \"0.063\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.14\", \"Magnetic polarization, Js</(T)\": \"1.30\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-2.43\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-127\", \"Formula\": \"Co5N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.063\", \"Energy relative to convex hull (eV/atom)\": \"0.063\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.25\", \"Magnetic polarization, Js</(T)\": \"1.41\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.04\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.97\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-1.01\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-128\", \"Formula\": \"Co5N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"0.063\", \"Energy relative to convex hull (eV/atom)\": \"0.063\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.26\", \"Magnetic polarization, Js</(T)\": \"1.42\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-0.51\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.26\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.24\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-129\", \"Formula\": \"Co5N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2\\u00a0[5]\", \"Formation energy (eV/atom)\": \"0.069\", \"Energy relative to convex hull (eV/atom)\": \"0.069\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.08\", \"Magnetic polarization, Js</(T)\": \"1.24\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.49\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.06\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.55\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-130\", \"Formula\": \"Co5N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/c\\u00a0[15]\", \"Formation energy (eV/atom)\": \"0.071\", \"Energy relative to convex hull (eV/atom)\": \"0.071\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.18\", \"Magnetic polarization, Js</(T)\": \"1.35\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.29\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.33\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"1.04\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-131\", \"Formula\": \"Co5N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.080\", \"Energy relative to convex hull (eV/atom)\": \"0.080\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.17\", \"Magnetic polarization, Js</(T)\": \"1.34\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.04\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.62\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.57\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-132\", \"Formula\": \"Co5N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"C222_1\\u00a0[20]\", \"Formation energy (eV/atom)\": \"0.082\", \"Energy relative to convex hull (eV/atom)\": \"0.082\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.08\", \"Magnetic polarization, Js</(T)\": \"1.24\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.08\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.04\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.04\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-133\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"0.062\", \"Energy relative to convex hull (eV/atom)\": \"0.062\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.15\", \"Magnetic polarization, Js</(T)\": \"1.32\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-0.24\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.68\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.92\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-134\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/mmm\\u00a0[123]\", \"Formation energy (eV/atom)\": \"0.062\", \"Energy relative to convex hull (eV/atom)\": \"0.062\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.35\", \"Magnetic polarization, Js</(T)\": \"1.51\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.54\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-135\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P-1\\u00a0[2]\", \"Formation energy (eV/atom)\": \"0.065\", \"Energy relative to convex hull (eV/atom)\": \"0.065\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.28\", \"Magnetic polarization, Js</(T)\": \"1.45\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-136\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"28\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmme\\u00a0[67]\", \"Formation energy (eV/atom)\": \"0.066\", \"Energy relative to convex hull (eV/atom)\": \"0.066\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.20\", \"Magnetic polarization, Js</(T)\": \"1.37\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.36\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-2.08\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-1.72\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-137\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"28\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Imma\\u00a0[74]\", \"Formation energy (eV/atom)\": \"0.073\", \"Energy relative to convex hull (eV/atom)\": \"0.073\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.22\", \"Magnetic polarization, Js</(T)\": \"1.38\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.87\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.90\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.03\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-138\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"3\", \"Atomic_sites per cell\": \"21\", \"Crystal system\": \"trigonal\", \"Space group [Number]\": \"R-3\\u00a0[148]\", \"Formation energy (eV/atom)\": \"0.078\", \"Energy relative to convex hull (eV/atom)\": \"0.078\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.20\", \"Magnetic polarization, Js</(T)\": \"1.37\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-0.29\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-139\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pnnm\\u00a0[58]\", \"Formation energy (eV/atom)\": \"0.081\", \"Energy relative to convex hull (eV/atom)\": \"0.081\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.21\", \"Magnetic polarization, Js</(T)\": \"1.37\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.06\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.68\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.62\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-140\", \"Formula\": \"Co6N\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"7\", \"Crystal system\": \"trigonal\", \"Space group [Number]\": \"P-31m\\u00a0[162]\", \"Formation energy (eV/atom)\": \"0.082\", \"Energy relative to convex hull (eV/atom)\": \"0.082\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.24\", \"Magnetic polarization, Js</(T)\": \"1.41\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.54\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-141\", \"Formula\": \"Co7N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P-1\\u00a0[2]\", \"Formation energy (eV/atom)\": \"0.051\", \"Energy relative to convex hull (eV/atom)\": \"0.051\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.19\", \"Magnetic polarization, Js</(T)\": \"1.36\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-142\", \"Formula\": \"Co7N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/c\\u00a0[15]\", \"Formation energy (eV/atom)\": \"0.057\", \"Energy relative to convex hull (eV/atom)\": \"0.057\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.19\", \"Magnetic polarization, Js</(T)\": \"1.35\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.15\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.79\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.63\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-143\", \"Formula\": \"Co7N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"0.057\", \"Energy relative to convex hull (eV/atom)\": \"0.057\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.38\", \"Magnetic polarization, Js</(T)\": \"1.53\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.18\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.02\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.16\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-144\", \"Formula\": \"Co7N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.058\", \"Energy relative to convex hull (eV/atom)\": \"0.058\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.36\", \"Magnetic polarization, Js</(T)\": \"1.51\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.02\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.38\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.39\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-145\", \"Formula\": \"Co7N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"32\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"0.069\", \"Energy relative to convex hull (eV/atom)\": \"0.069\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.28\", \"Magnetic polarization, Js</(T)\": \"1.44\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.11\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.61\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.51\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-146\", \"Formula\": \"Co8N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"cubic\", \"Space group [Number]\": \"Fm-3m\\u00a0[225]\", \"Formation energy (eV/atom)\": \"0.039\", \"Energy relative to convex hull (eV/atom)\": \"0.039\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.29\", \"Magnetic polarization, Js</(T)\": \"1.45\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \"0.00\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-147\", \"Formula\": \"Co8N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"18\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"0.041\", \"Energy relative to convex hull (eV/atom)\": \"0.041\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.23\", \"Magnetic polarization, Js</(T)\": \"1.39\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-0.54\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.36\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.17\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-148\", \"Formula\": \"Co8N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"18\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2/m\\u00a0[12]\", \"Formation energy (eV/atom)\": \"0.041\", \"Energy relative to convex hull (eV/atom)\": \"0.041\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.35\", \"Magnetic polarization, Js</(T)\": \"1.51\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"0.02\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.07\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.09\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-149\", \"Formula\": \"Co8N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"18\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"0.043\", \"Energy relative to convex hull (eV/atom)\": \"0.043\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.30\", \"Magnetic polarization, Js</(T)\": \"1.45\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.98\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-1.50\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.52\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-150\", \"Formula\": \"Co8N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"18\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"P2_12_12\\u00a0[18]\", \"Formation energy (eV/atom)\": \"0.044\", \"Energy relative to convex hull (eV/atom)\": \"0.044\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.22\", \"Magnetic polarization, Js</(T)\": \"1.38\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-0.19\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.06\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.14\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-166\", \"Formula\": \"ZrCo5\", \"Formula units_per cell\": \"6\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"trigonal\", \"Space group [Number]\": \"R32\\u00a0[155]\", \"Formation energy (eV/atom)\": \"-0.123\", \"Energy relative to convex hull (eV/atom)\": \"0.068\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.00\", \"Magnetic polarization, Js</(T)\": \"0.94\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.31\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevMaterials.2.084410\"}, {\"Materials ID\": \"MMD-167\", \"Formula\": \"ZrCo5\", \"Formula units_per cell\": \"6\", \"Atomic_sites per cell\": \"36\", \"Crystal system\": \"trigonal\", \"Space group [Number]\": \"R3m\\u00a0[160]\", \"Formation energy (eV/atom)\": \"-0.135\", \"Energy relative to convex hull (eV/atom)\": \"0.055\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.05\", \"Magnetic polarization, Js</(T)\": \"0.96\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.07\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevMaterials.2.084410\"}, {\"Materials ID\": \"MMD-168\", \"Formula\": \"ZrCo5\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"hexagonal\", \"Space group [Number]\": \"P6_322\\u00a0[182]\", \"Formation energy (eV/atom)\": \"-0.128\", \"Energy relative to convex hull (eV/atom)\": \"0.063\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.01\", \"Magnetic polarization, Js</(T)\": \"0.94\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.05\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevMaterials.2.084410\"}, {\"Materials ID\": \"MMD-169\", \"Formula\": \"ZrCo5\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"hexagonal\", \"Space group [Number]\": \"P-62c\\u00a0[190]\", \"Formation energy (eV/atom)\": \"-0.128\", \"Energy relative to convex hull (eV/atom)\": \"0.063\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.01\", \"Magnetic polarization, Js</(T)\": \"0.94\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.24\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevMaterials.2.084410\"}, {\"Materials ID\": \"MMD-170\", \"Formula\": \"ZrCo5\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"6\", \"Crystal system\": \"hexagonal\", \"Space group [Number]\": \"P6/mmm\\u00a0[191]\", \"Formation energy (eV/atom)\": \"-0.131\", \"Energy relative to convex hull (eV/atom)\": \"0.060\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.08\", \"Magnetic polarization, Js</(T)\": \"0.97\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.01\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevMaterials.2.084410\"}, {\"Materials ID\": \"MMD-4\", \"Formula\": \"FeCo5N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2\\u00a0[5]\", \"Formation energy (eV/atom)\": \"0.040\", \"Energy relative to convex hull (eV/atom)\": \"0.073\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.80\", \"Magnetic polarization, Js</(T)\": \"0.95\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.29\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.34\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.05\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-5\", \"Formula\": \"FeCo5N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"0.063\", \"Energy relative to convex hull (eV/atom)\": \"0.096\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.06\", \"Magnetic polarization, Js</(T)\": \"1.25\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.63\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.35\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.71\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-6\", \"Formula\": \"FeCo5N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"0.066\", \"Energy relative to convex hull (eV/atom)\": \"0.099\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.07\", \"Magnetic polarization, Js</(T)\": \"1.26\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.68\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.96\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-1.64\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-7\", \"Formula\": \"FeCo2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"C222_1\\u00a0[20]\", \"Formation energy (eV/atom)\": \"0.016\", \"Energy relative to convex hull (eV/atom)\": \"0.083\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.99\", \"Magnetic polarization, Js</(T)\": \"1.17\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-1.63\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.46\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"1.17\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-8\", \"Formula\": \"FeCo2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"Cc\\u00a0[9]\", \"Formation energy (eV/atom)\": \"0.018\", \"Energy relative to convex hull (eV/atom)\": \"0.084\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"0.92\", \"Magnetic polarization, Js</(T)\": \"1.09\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"-0.83\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.98\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.15\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-9\", \"Formula\": \"FeCo2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"0.040\", \"Energy relative to convex hull (eV/atom)\": \"0.107\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.14\", \"Magnetic polarization, Js</(T)\": \"1.33\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.64\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"2.17\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.53\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-10\", \"Formula\": \"Fe3Co3N2\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"8\", \"Crystal system\": \"triclinic\", \"Space group [Number]\": \"P1\\u00a0[1]\", \"Formation energy (eV/atom)\": \"-0.005\", \"Energy relative to convex hull (eV/atom)\": \"0.079\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.06\", \"Magnetic polarization, Js</(T)\": \"1.25\", \"Magnetic easy axis\": \".\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-11\", \"Formula\": \"Fe3Co3N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"0.009\", \"Energy relative to convex hull (eV/atom)\": \"0.093\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.20\", \"Magnetic polarization, Js</(T)\": \"1.40\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"2.16\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"2.02\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.15\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-12\", \"Formula\": \"Fe3Co3N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"0.012\", \"Energy relative to convex hull (eV/atom)\": \"0.096\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.37\", \"Magnetic polarization, Js</(T)\": \"1.59\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"2.21\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"2.14\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.08\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-13\", \"Formula\": \"Fe2CoN\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2\\u00a0[5]\", \"Formation energy (eV/atom)\": \"-0.028\", \"Energy relative to convex hull (eV/atom)\": \"0.073\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.28\", \"Magnetic polarization, Js</(T)\": \"1.50\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-1.36\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-1.30\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.06\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-14\", \"Formula\": \"Fe2CoN\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmcm\\u00a0[63]\", \"Formation energy (eV/atom)\": \"-0.009\", \"Energy relative to convex hull (eV/atom)\": \"0.092\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.50\", \"Magnetic polarization, Js</(T)\": \"1.72\", \"Magnetic easy axis\": \"b\", \"Magnetic anisotropy constants:Ka-c\": \"1.01\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-1.80\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-2.81\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-15\", \"Formula\": \"Fe2CoN\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.002\", \"Energy relative to convex hull (eV/atom)\": \"0.099\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.40\", \"Magnetic polarization, Js</(T)\": \"1.62\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"2.02\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"2.02\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.00\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-16\", \"Formula\": \"Fe5CoN2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"monoclinic\", \"Space group [Number]\": \"C2\\u00a0[5]\", \"Formation energy (eV/atom)\": \"-0.047\", \"Energy relative to convex hull (eV/atom)\": \"0.045\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.42\", \"Magnetic polarization, Js</(T)\": \"1.65\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-1.08\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.48\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.60\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-17\", \"Formula\": \"Fe5CoN2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.015\", \"Energy relative to convex hull (eV/atom)\": \"0.077\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.49\", \"Magnetic polarization, Js</(T)\": \"1.73\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.47\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"2.56\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"1.09\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-18\", \"Formula\": \"Fe5CoN2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"16\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Cmmm\\u00a0[65]\", \"Formation energy (eV/atom)\": \"-0.008\", \"Energy relative to convex hull (eV/atom)\": \"0.084\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.55\", \"Magnetic polarization, Js</(T)\": \"1.77\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-1.37\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.30\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"1.07\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-19\", \"Formula\": \"FeCo7N2\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/mmm\\u00a0[123]\", \"Formation energy (eV/atom)\": \"0.035\", \"Energy relative to convex hull (eV/atom)\": \"0.062\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.37\", \"Magnetic polarization, Js</(T)\": \"1.54\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-0.40\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-20\", \"Formula\": \"FeCo7N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/mmm\\u00a0[139]\", \"Formation energy (eV/atom)\": \"0.043\", \"Energy relative to convex hull (eV/atom)\": \"0.069\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.37\", \"Magnetic polarization, Js</(T)\": \"1.55\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.62\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-21\", \"Formula\": \"FeCo3N\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"5\", \"Crystal system\": \"cubic\", \"Space group [Number]\": \"Pm-3m\\u00a0[221]\", \"Formation energy (eV/atom)\": \"-0.004\", \"Energy relative to convex hull (eV/atom)\": \"0.049\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.48\", \"Magnetic polarization, Js</(T)\": \"1.66\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \".\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \"0.00\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-22\", \"Formula\": \"FeCo3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4mm\\u00a0[107]\", \"Formation energy (eV/atom)\": \"0.011\", \"Energy relative to convex hull (eV/atom)\": \"0.064\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.47\", \"Magnetic polarization, Js</(T)\": \"1.65\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.27\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-23\", \"Formula\": \"Fe3Co5N2\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmmm\\u00a0[47]\", \"Formation energy (eV/atom)\": \"-0.024\", \"Energy relative to convex hull (eV/atom)\": \"0.043\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.55\", \"Magnetic polarization, Js</(T)\": \"1.73\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-0.07\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.07\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.01\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-24\", \"Formula\": \"Fe3Co5N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/mmm\\u00a0[139]\", \"Formation energy (eV/atom)\": \"-0.011\", \"Energy relative to convex hull (eV/atom)\": \"0.056\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.55\", \"Magnetic polarization, Js</(T)\": \"1.73\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.94\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-25\", \"Formula\": \"Fe3Co5N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I-4m2\\u00a0[119]\", \"Formation energy (eV/atom)\": \"0.002\", \"Energy relative to convex hull (eV/atom)\": \"0.068\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.51\", \"Magnetic polarization, Js</(T)\": \"1.70\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.58\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-26\", \"Formula\": \"Fe2Co2N\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"5\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/mmm\\u00a0[123]\", \"Formation energy (eV/atom)\": \"-0.040\", \"Energy relative to convex hull (eV/atom)\": \"0.041\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.60\", \"Magnetic polarization, Js</(T)\": \"1.78\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-0.31\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-27\", \"Formula\": \"Fe2Co2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Imm2\\u00a0[44]\", \"Formation energy (eV/atom)\": \"-0.019\", \"Energy relative to convex hull (eV/atom)\": \"0.062\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.58\", \"Magnetic polarization, Js</(T)\": \"1.77\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.92\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.85\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.07\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-28\", \"Formula\": \"Fe5Co3N2\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmmm\\u00a0[47]\", \"Formation energy (eV/atom)\": \"-0.038\", \"Energy relative to convex hull (eV/atom)\": \"0.056\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.65\", \"Magnetic polarization, Js</(T)\": \"1.82\", \"Magnetic easy axis\": \"a\", \"Magnetic anisotropy constants:Ka-c\": \"-0.62\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.75\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.13\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-29\", \"Formula\": \"Fe5Co3N2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/mmm\\u00a0[139]\", \"Formation energy (eV/atom)\": \"-0.025\", \"Energy relative to convex hull (eV/atom)\": \"0.069\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.68\", \"Magnetic polarization, Js</(T)\": \"1.86\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"2.01\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-30\", \"Formula\": \"Fe3CoN\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmm2\\u00a0[25]\", \"Formation energy (eV/atom)\": \"-0.036\", \"Energy relative to convex hull (eV/atom)\": \"0.054\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.76\", \"Magnetic polarization, Js</(T)\": \"1.92\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.23\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"-0.46\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.68\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-31\", \"Formula\": \"Fe3CoN\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4mm\\u00a0[107]\", \"Formation energy (eV/atom)\": \"-0.033\", \"Energy relative to convex hull (eV/atom)\": \"0.057\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.73\", \"Magnetic polarization, Js</(T)\": \"1.91\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.96\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-32\", \"Formula\": \"Fe7CoN2\", \"Formula units_per cell\": \"1\", \"Atomic_sites per cell\": \"10\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/mmm\\u00a0[123]\", \"Formation energy (eV/atom)\": \"-0.037\", \"Energy relative to convex hull (eV/atom)\": \"0.037\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.87\", \"Magnetic polarization, Js</(T)\": \"2.01\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.85\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-33\", \"Formula\": \"Fe7CoN2\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"20\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4mm\\u00a0[107]\", \"Formation energy (eV/atom)\": \"-0.032\", \"Energy relative to convex hull (eV/atom)\": \"0.042\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.83\", \"Magnetic polarization, Js</(T)\": \"2.00\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.88\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-34\", \"Formula\": \"FeCo4N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"0.014\", \"Energy relative to convex hull (eV/atom)\": \"0.058\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.41\", \"Magnetic polarization, Js</(T)\": \"1.57\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.09\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.92\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.17\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-35\", \"Formula\": \"FeCo4N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"0.025\", \"Energy relative to convex hull (eV/atom)\": \"0.070\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.39\", \"Magnetic polarization, Js</(T)\": \"1.56\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.99\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.02\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.03\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-36\", \"Formula\": \"FeCo4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"12\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"I4/m\\u00a0[87]\", \"Formation energy (eV/atom)\": \"0.028\", \"Energy relative to convex hull (eV/atom)\": \"0.072\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.28\", \"Magnetic polarization, Js</(T)\": \"1.46\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-1.89\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-37\", \"Formula\": \"Fe2Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.012\", \"Energy relative to convex hull (eV/atom)\": \"0.055\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.52\", \"Magnetic polarization, Js</(T)\": \"1.68\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.40\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.24\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.16\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-38\", \"Formula\": \"Fe2Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.010\", \"Energy relative to convex hull (eV/atom)\": \"0.057\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.52\", \"Magnetic polarization, Js</(T)\": \"1.68\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.31\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.47\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.15\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-39\", \"Formula\": \"Fe2Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.009\", \"Energy relative to convex hull (eV/atom)\": \"0.058\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.51\", \"Magnetic polarization, Js</(T)\": \"1.67\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.39\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.89\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.49\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-40\", \"Formula\": \"Fe2Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.009\", \"Energy relative to convex hull (eV/atom)\": \"0.058\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.53\", \"Magnetic polarization, Js</(T)\": \"1.68\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.18\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.48\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.30\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-41\", \"Formula\": \"Fe2Co3N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.008\", \"Energy relative to convex hull (eV/atom)\": \"0.059\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.51\", \"Magnetic polarization, Js</(T)\": \"1.67\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.39\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.67\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.28\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-42\", \"Formula\": \"Fe3Co2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.018\", \"Energy relative to convex hull (eV/atom)\": \"0.071\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.57\", \"Magnetic polarization, Js</(T)\": \"1.74\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.90\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.09\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.18\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-43\", \"Formula\": \"Fe3Co2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.014\", \"Energy relative to convex hull (eV/atom)\": \"0.076\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.61\", \"Magnetic polarization, Js</(T)\": \"1.78\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.65\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.48\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.17\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-44\", \"Formula\": \"Fe3Co2N\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.014\", \"Energy relative to convex hull (eV/atom)\": \"0.076\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.60\", \"Magnetic polarization, Js</(T)\": \"1.77\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.88\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.05\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.17\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-45\", \"Formula\": \"Fe4CoN\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.018\", \"Energy relative to convex hull (eV/atom)\": \"0.060\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.85\", \"Magnetic polarization, Js</(T)\": \"1.99\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.12\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.15\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.04\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-46\", \"Formula\": \"Fe4CoN\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"12\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.014\", \"Energy relative to convex hull (eV/atom)\": \"0.064\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.83\", \"Magnetic polarization, Js</(T)\": \"1.98\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.89\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.88\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.01\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-47\", \"Formula\": \"Fe4CoN\", \"Formula units_per cell\": \"4\", \"Atomic_sites per cell\": \"24\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Amm2\\u00a0[38]\", \"Formation energy (eV/atom)\": \"-0.013\", \"Energy relative to convex hull (eV/atom)\": \"0.065\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.83\", \"Magnetic polarization, Js</(T)\": \"1.97\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"1.47\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"1.40\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"-0.07\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-48\", \"Formula\": \"FeCo5N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4mm\\u00a0[99]\", \"Formation energy (eV/atom)\": \"0.015\", \"Energy relative to convex hull (eV/atom)\": \"0.053\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.49\", \"Magnetic polarization, Js</(T)\": \"1.64\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.53\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-49\", \"Formula\": \"FeCo5N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/mmm\\u00a0[123]\", \"Formation energy (eV/atom)\": \"0.022\", \"Energy relative to convex hull (eV/atom)\": \"0.060\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.47\", \"Magnetic polarization, Js</(T)\": \"1.63\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-0.01\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-50\", \"Formula\": \"FeCo5N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4mm\\u00a0[99]\", \"Formation energy (eV/atom)\": \"0.024\", \"Energy relative to convex hull (eV/atom)\": \"0.062\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.46\", \"Magnetic polarization, Js</(T)\": \"1.61\", \"Magnetic easy axis\": \"ab plane\", \"Magnetic anisotropy constants:Ka-c\": \"-0.43\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-51\", \"Formula\": \"Fe2Co4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"tetragonal\", \"Space group [Number]\": \"P4/mmm\\u00a0[123]\", \"Formation energy (eV/atom)\": \"-0.017\", \"Energy relative to convex hull (eV/atom)\": \"0.041\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.57\", \"Magnetic polarization, Js</(T)\": \"1.72\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.54\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \".\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-52\", \"Formula\": \"Fe2Co4N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmm2\\u00a0[25]\", \"Formation energy (eV/atom)\": \"-0.012\", \"Energy relative to convex hull (eV/atom)\": \"0.046\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.56\", \"Magnetic polarization, Js</(T)\": \"1.71\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.90\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.97\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.07\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}, {\"Materials ID\": \"MMD-53\", \"Formula\": \"Fe3Co3N\", \"Formula units_per cell\": \"2\", \"Atomic_sites per cell\": \"14\", \"Crystal system\": \"orthorhombic\", \"Space group [Number]\": \"Pmmm\\u00a0[47]\", \"Formation energy (eV/atom)\": \"-0.019\", \"Energy relative to convex hull (eV/atom)\": \"0.058\", \"Structure search\": \"AGA search\", \"Averaged magnetic moment (\\u03bcB/atom)\": \"1.59\", \"Magnetic polarization, Js</(T)\": \"1.74\", \"Magnetic easy axis\": \"c\", \"Magnetic anisotropy constants:Ka-c\": \"0.70\", \"Magnetic anisotropy constants:Kb-c (MJ/m3)\": \"0.71\", \"Magnetic anisotropy constants:Kb-a (MJ/m3)\": \"0.01\", \"Magnetic anisotropy constants:Kd-a (MJ/m3)\": \".\", \"Curie temperature, TC(K)\": \".\", \"Methods\": \"DFT\", \"References\": \"https://doi.org/10.1103/PhysRevB.94.224424\"}]"
  },
  {
    "path": "dataset/MoosaviCp/MoosaviCp.csv",
    "content": "MOF structural features and topology,composition,Cv_gravimetric_300.00 (gravimetric heat capacity at 300 K),pCv_250.00 (predicted gravimetric heat capacity at 250 K),pCv_275.00 (predicted gravimetric heat capacity at 275 K),pCv_300.00 (predicted gravimetric heat capacity at 300 K),pCv_325.00 (predicted gravimetric heat capacity at 325 K),pCv_350.00 (predicted gravimetric heat capacity at 350 K),pCv_375.00 (predicted gravimetric heat capacity at 375 K),pCv_400.00 (predicted gravimetric heat capacity at 400 K)\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",Co2 H4 C8 O8,0.724853926,,,,,,,\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",Co2 H6 C6 O12,0.85097406,,,,,,,\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",Cu4 H8 C8 N12,0.676886037,,,,,,,\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",Cd3 H6 C18 O12,0.608760737,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",Co2 H12 C16 O10,0.847654495,,,,,,,\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",Cu4 H8 C12 O16,0.723035059,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",Cu2 H4 C20 O16,0.808027702,,,,,,,\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",Cd4 H2 C18 N2 O16,0.575099801,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",Ni2 H4 C20 O16,0.817186976,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",Co2 H4 C20 O16,0.795803138,,,,,,,\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",Cd4 H16 C12 N12,0.701243308,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",Al2 H4 C20 O18,0.931354395,,,,,,,\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",Zn4 H8 C12 N12 O8,0.720706418,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",Co4 H4 C20 O16,0.724504144,,,,,,,\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",Zn8 H12 C8 N12 O4,0.642031443,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",Cd4 H6 C18 N8 O10,0.591632576,,,,,,,\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",Cu2 H16 C22 N6,0.876427721,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",Zn5 P2 H8 C16 O16,0.694355732,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",Cu4 H8 C18 N8 O10,0.718767158,,,,,,,\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",Ni3 H20 C16 O10,0.798729637,,,,,,,\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",Cu2 H16 C20 N12,0.84624624,,,,,,,\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",Ni3 H16 C18 O14,0.860334193,,,,,,,\n\"linker [O-]C=O, nodes [Fe], topology pcu\",Fe4 H12 C12 O24,0.674034815,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",Cu6 H6 C24 O18,0.689623696,,,,,,,\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",Cu2 H16 C24 N4 O8,0.845181896,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",Zn6 H6 C24 O18,0.690649103,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",Ni6 H6 C24 O18,0.713069679,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",Mn6 H6 C24 O18,0.742935026,,,,,,,\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",Cd6 H12 C12 N18 Cl6,0.512272809,,,,,,,\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",Cu2 P4 H20 C16 O12,0.870048391,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",Cd6 H6 C24 O18,0.54572684,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",Cd2 H16 C22 N6 O8,0.745259778,,,,,,,\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",Gd2 H18 C24 O12,0.660910534,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",Co2 H18 C26 N8 O4,0.886918341,,,,,,,\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",Ni2 H21 C23 N5 O8,0.890669452,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",Zn4 H12 C32 O16,0.765187926,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",Co6 H6 C24 N12 O18,0.802825749,,,,,,,\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",Mn2 H12 C36 O16,0.908266016,,,,,,,\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",Co4 H12 C34 O18,0.812287627,,,,,,,\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",Co4 H14 C30 N2 O20,0.825222945,,,,,,,\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",Co2 H24 C32 N4 O8,0.952753545,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",Ga4 H16 C32 O20,0.795314824,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",Ga4 H16 C32 O20,0.808953888,,,,,,,\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",In4 H12 C36 O28,0.684423051,,,,,,,\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",Zn2 H34 C36 N8 O4,0.965559867,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",In6 H8 C40 O36,0.664555524,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",Fe6 H30 C30 O24,0.91340595,,,,,,,\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",Zn4 H24 C48 O16,0.820125808,,,,,,,\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",In4 H24 C48 N8 O16,0.732535376,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",In2 H28 C56 O16,0.843409061,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",Fe6 H24 C48 O26,0.854477993,,,,,,,\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",Cu6 H42 C40 N16,0.937748442,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",Fe6 H28 C64 O30,0.844221619,,,,,,,\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",Fe2 H48 C30 N48,0.987516358,,,,,,,\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",Mn12 H40 C32 O48,0.897334191,,,,,,,\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",Cd6 H24 C68 O36,0.739871388,,,,,,,\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",Eu4 H48 C68 O16,0.763143177,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",Co4 H36 C60 N20 O16,0.899010694,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",Mn8 H16 C64 N8 O48,0.80177265,,,,,,,\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",Mn10 H28 C56 N8 O44,0.847597122,,,,,,,\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",Ni8 H40 C58 N6 O34,0.832210439,,,,,,,\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",Zn10 H24 C52 N28 O32,0.770836596,,,,,,,\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",Zn2 H60 C72 N12,1.009817542,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",Cu6 H48 C63 N6 O24,0.870523493,,,,,,,\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",Cu3 H42 C66 N36,0.907069352,,,,,,,\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",Mn9 H30 C66 N12 O30,0.844993575,,,,,,,\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",Zn4 H48 C72 N8 O16,0.913999797,,,,,,,\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",Cd4 Ni4 H72 C44 N24,0.809097569,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",Zn4 H32 C56 N32 O24,0.875557816,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",Ni2 H2 C10 O8,0.700711314,,,,,,,\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",Ni2 H8 C12 O8,0.791703538,,,,,,,\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",Cu2 H8 C12 N8,0.712711387,,,,,,,\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",Co2 H8 C12 O8,0.797181306,,,,,,,\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",Cd1 Ni1 H16 C10 N6,0.828969829,,,,,,,\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",Zn2 H8 C4 N20,0.793059155,,,,,,,\n\"linker [C]#N, nodes [Cd], topology pts\",Cd4 H12 C8 N12,0.755841626,,,,,,,\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",Mn1 H12 C18 N6,0.9209987,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",Fe2 H10 C16 O10,0.788657275,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",Cu2 H8 C16 N8 O4,0.758913982,,,,,,,\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",Cu2 H4 C16 N8 O4 F4,0.737770036,,,,,,,\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",Cd2 H12 C18 S6,0.636040507,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",Al2 H10 C16 O10,0.912714153,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",Ga2 H10 C16 O10,0.77441443,,,,,,,\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",Cd4 P4 H4 C4 O24,0.600416673,,,,,,,\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",Mn2 H4 C16 S4 N8 O8,0.755118167,,,,,,,\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",Zn2 H4 C16 S4 N8 O8,0.738759983,,,,,,,\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",Cd2 H16 C12 N12 Cl2,0.720532665,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",Cd4 H6 C18 Cl4 O12,0.582796447,,,,,,,\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",Zn2 P4 H12 C12 O16,0.820981288,,,,,,,\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",K2 Cd2 H4 Ru4 C8 O26,0.564751976,,,,,,,\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",Zn5 H10 C16 O18,0.75517978,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",Ni3 H8 C20 O18,0.783790469,,,,,,,\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",Zn3 H12 C20 N6 O8,0.785858042,,,,,,,\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",Fe1 H12 C12 N24,0.906405772,,,,,,,\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",U3 Zn2 P8 H8 C4 O24,0.444768986,,,,,,,\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",Co2 H12 C24 N8 F4,0.81495135,,,,,,,\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",Gd2 H12 C24 O12,0.628011001,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",Co3 H8 C20 N12 O8,0.781701814,,,,,,,\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",Mn3 H12 C21 O15,0.886516545,,,,,,,\n\"linker [O-]C=O, nodes [Zn], topology pcu\",Zn4 H12 C12 O24,0.645931211,,,,,,,\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",Al4 H12 C16 O20,0.980076572,,,,,,,\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",Mn4 H12 C12 O24,0.883757399,,,,,,,\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",Mn2 P4 H20 C16 O12,0.899902065,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",Co6 H6 C24 O18,0.715644717,,,,,,,\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",Cd3 H8 C24 O20,0.686975633,,,,,,,\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",Ni4 H12 C20 N8 Cl4 O8,0.736052691,,,,,,,\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",Ca2 Cu2 H8 C24 S4 O16,0.79038672,,,,,,,\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",Cu4 H8 C24 S4 O16,0.734057713,,,,,,,\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",Co2 H20 C24 N4 O6 F2,0.91616323,,,,,,,\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",Al4 P6 H12 C18 O18,0.812750828,,,,,,,\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",Ni4 H20 C20 N8 O8,0.816602405,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",Mn2 H18 C30 N2 O8,0.875256356,,,,,,,\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",Mn2 Ga4 P6 H4 C8 O40,0.735122499,,,,,,,\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",V4 Co2 H20 C24 N4 O10,0.819407675,,,,,,,\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",Fe6 H6 C24 O30,0.799893695,,,,,,,\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",Zn2 Ni2 H16 C30 N14 O2,0.909608714,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",Ni4 H12 C32 O20,0.812693276,,,,,,,\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",Ni4 H16 C28 N4 O18,0.813947367,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",Al4 H16 C32 O20,0.936838277,,,,,,,\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",Li8 H12 C32 N4 O16,1.086651319,,,,,,,\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",Ni2 H22 C36 N4 O9,0.899570347,,,,,,,\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",Ce2 H18 C36 N6 O12,0.73470225,,,,,,,\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",Sr2 Ni2 H20 C28 N4 O20,0.820405532,,,,,,,\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",Zn2 H30 C34 N4 O8,0.959708213,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",Mn8 H12 C36 Cl4 O24,0.72546289,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",In4 Co2 H12 C36 Br4 O28,0.59852749,,,,,,,\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",Cu8 H16 C32 N16 O16,0.674554829,,,,,,,\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",Cd2 H30 C30 S2 N18 O8,0.807577262,,,,,,,\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",Zn6 H20 C46 O22,0.783630688,,,,,,,\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",Cd4 H32 C48 N8 O16,0.755945681,,,,,,,\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",In4 H16 C48 S8 O32,0.73939454,,,,,,,\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",Cu4 H24 C52 N12 O16,0.829734793,,,,,,,\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",K4 H44 C36 S4 N4 O18,0.980398766,,,,,,,\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",Ag6 H36 C48 N24,0.712794485,,,,,,,\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",Na6 Eu1 H24 C40 S8 N8 Cl1 O36,0.798633201,,,,,,,\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",Fe2 H48 C54 S4 N12 O8,0.987820759,,,,,,,\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",Zn2 H48 C30 N48,0.972952881,,,,,,,\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",Ba4 H34 C64 O38,0.777219281,,,,,,,\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",Mn4 H32 C76 N8 O24,0.86868107,,,,,,,\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",Cu4 H64 C64 S8 Br4,0.809495392,,,,,,,\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",V12 Ni8 H24 C40 N16 O46,0.756509048,,,,,,,\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",Zn8 H32 C68 O40,0.803413669,,,,,,,\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",Cd4 H32 C56 N32 O24,0.794519436,,,,,,,\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,22.41778292,22.59587834,22.73372187,22.84252961,22.92988436,23.00105521,23.05979268\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,22.94001945,23.07542439,23.179683,23.26162209,23.32716229,23.38039057,23.4241995\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,22.37085474,22.54875225,22.68645208,22.79515281,22.88242577,22.95353254,23.01221861\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,23.21255488,23.3475588,23.45149011,23.53316104,23.59848007,23.65152447,23.69517927\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.358631929,4.041630584,4.743833748,5.447608008,6.139497181,6.81005814,7.453293232\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.258266591,3.912362019,4.591461334,5.277883907,5.95767707,6.620705301,7.260235299\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.057125904,3.708413928,4.389588086,5.081767039,5.76984057,6.44270815,7.092900635\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.068916027,3.522108747,4.014235683,4.536515273,5.079373933,5.633800106,6.192072281\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.04719062,3.5038994,3.999058512,4.52376828,5.068222662,5.623155869,6.18062871\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.026158135,3.430691813,3.880841124,4.367218083,4.879616698,5.408313377,5.944821336\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.203556357,3.627218725,4.095710157,4.598760127,5.125686013,5.666646159,6.213293683\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.345682991,3.807845085,4.309674699,4.839781728,5.38718797,5.942239653,6.497042678\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.421800845,3.89350958,4.403633061,4.940663616,5.493635395,6.053014426,6.611094672\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.546931762,4.114046212,4.699494354,5.291514358,5.880500108,6.458874282,7.020883815\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.902537172,4.653678606,5.389161938,6.096820529,6.769885422,7.405244304,8.002162404\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.740008485,4.43178396,5.135049092,5.833888343,6.516524883,7.174957241,7.804338007\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.493233588,4.147752446,4.823818308,5.504861131,6.17769344,6.832709294,7.463548203\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.511848668,4.162425823,4.82901917,5.497266822,6.155922315,6.796855959,7.414706712\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,6.86935704,7.45981145,8.011779611,8.532282573,9.025022301,9.491742911,9.933214099\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.446404995,3.995357738,4.577155461,5.177915716,5.785121356,6.388563199,6.980566975\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.011943596,3.424313711,3.879435056,4.369042006,4.883601615,5.413764347,5.951235528\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.195675695,3.634769487,4.115406909,4.628041095,5.162327296,5.708554594,6.258420785\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.133602949,3.590344713,4.086957914,4.612927803,5.157783892,5.71210514,6.268038043\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.264892206,3.732400071,4.238076425,4.771122075,5.320982108,5.878293484,6.435352246\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,5.65640586,6.208616341,6.745185446,7.266415907,7.7716362,8.259606425,8.728925315\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,4.001149775,4.753228501,5.487048138,6.191121624,6.859296627,7.488938585,8.079638943\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.326293924,4.007973633,4.709158033,5.412214808,6.103678826,6.774093811,7.417447386\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.248145835,3.90261856,4.582079686,5.268827833,5.948906825,6.612185605,7.251937966\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.053684263,3.704923187,4.386001754,5.078057627,5.76600192,6.438751483,7.088848752\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.062071819,3.514591443,4.006113589,4.527866182,5.070279475,5.624340661,6.182323261\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.052218441,3.509109492,4.004459432,4.529333393,5.073905261,5.628900789,6.186380212\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,2.9942019,3.398405723,3.84826515,4.334473838,4.84686811,5.375739351,5.912597887\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.181306176,3.606344618,4.076177588,4.580522672,5.108680993,5.650797848,6.19851863\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.343346293,3.804964372,4.306458139,4.83642019,5.383834715,5.939005014,6.493997042\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.435556878,3.909311026,4.421354226,4.960067569,5.5144074,6.074795664,6.633510769\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.55745989,4.124497647,4.709675805,5.301295915,5.889796608,6.467632207,7.029072204\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,4.115896644,4.879268534,5.620143019,6.328181017,6.998157062,7.628175228,8.218429095\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.633974586,4.323692623,5.025799249,5.724204562,6.406966581,7.065941445,7.696165286\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.473445302,4.128256727,4.804559774,5.485770721,6.158702479,6.813756407,7.444581903\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.530435624,4.181139915,4.847510342,5.515264691,6.173204615,6.813228274,7.429990922\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.052580029,7.598431298,8.110739585,8.59645992,9.058806151,9.498925132,9.91701399\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.588599161,4.146286347,4.734137434,5.33834983,5.946660584,6.549186995,7.138590612\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,2.983114898,3.39474856,3.84921588,4.338332486,4.852621163,5.38276353,5.920475679\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.184524766,3.6248397,4.106664668,4.620409597,5.15570179,5.702814971,6.253441102\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.183596364,3.643989178,4.143771083,4.672247688,5.218846148,5.774106906,6.330185543\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,3.27595126,3.740721575,4.243770642,4.774411091,5.322148968,5.877643439,6.433186396\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,5.642108479,6.193811173,6.730531782,7.252313781,7.758304473,8.247143124,8.717351398\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,4.306775875,5.08275373,5.83003724,6.539451228,7.206867753,7.83125773,8.413408417\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.824506321,8.592059534,9.350067259,10.09587198,10.82561776,11.53515107,12.22065988\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.546613847,8.323913261,9.088265304,9.837522134,10.56875058,11.27871329,11.96433321\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.518475827,10.3083469,11.06446626,11.78609606,12.47274807,13.12418167,13.74045413\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.531142588,10.32431196,11.08533766,11.8125752,12.50488168,13.16160608,13.78258557\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.929184836,8.779082652,9.609776903,10.41634528,11.19457326,11.94104912,12.65325078\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.316819549,10.11345448,10.88216345,11.61964197,12.3235249,12.99232999,13.62536262\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.508534589,10.300375,11.07189783,11.81701195,12.5305397,13.208751,13.84942883\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.4215404,11.04503442,11.67259833,12.29692296,12.91039404,13.50641847,14.07994278\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.69786062,11.31168267,11.93189856,12.54994357,13.15744829,13.74740298,14.31455764\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,8.137794063,8.921749138,9.689726736,10.43996919,11.16970172,11.87581434,12.55540222\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.338764165,8.142409683,8.937348712,9.717605884,10.47804764,11.21435182,11.92305645\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.12019553,10.87450003,11.59641995,12.28546141,12.94133929,13.56393187,14.15333246\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.728115362,10.50810334,11.25486911,11.96743896,12.64522453,13.28799141,13.89585848\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,8.152657525,9.002523704,9.831179921,10.63425986,11.40789052,12.14890593,12.85498518\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.381386486,10.18383819,10.95680908,11.69724673,12.40300413,13.07279026,13.7060768\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.340856515,10.08568222,10.79860005,11.48135963,12.13477372,12.75910585,13.3543917\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.09089529,10.77648088,11.45652547,12.1248258,12.77478777,13.40079016,13.99869474\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.6729076,11.29315632,11.91628906,12.5351357,13.14225019,13.73122016,14.29717001\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.782298761,8.548887243,9.305865611,10.05066347,10.77949082,11.48823561,12.17310586\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.352581855,8.131853751,8.898571335,9.650292683,10.38388456,11.09598707,11.78345963\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.380595899,10.17056791,10.92679388,11.64853474,12.33530668,12.98687484,13.60330132\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.488693766,10.28235626,11.04373424,11.77121164,12.46367249,13.12048831,13.74151405\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,7.918583097,8.767992078,9.598160304,10.40421515,11.18197695,11.92805549,12.63993921\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.318261704,10.1152105,10.88433094,11.62227022,12.32662595,12.99588934,13.62934852\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.480566006,10.27087356,11.04123204,11.78549764,12.49844005,13.17628034,13.81675839\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.38408281,11.00852401,11.63656667,12.26108827,12.87459662,13.4705767,14.04402345\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.67954137,11.29424197,11.91528073,12.53407183,13.14223232,13.7327464,14.3003641\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,8.063840338,8.847030207,9.614759425,10.36513317,11.09525914,11.80193472,12.4821859\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,6.787013893,7.588787477,8.382207415,9.161235513,9.920698404,10.65624421,11.36438522\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.650193914,10.40309432,11.12381194,11.81184122,12.46688588,13.08881138,13.67769612\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.524411731,10.30341411,11.04947757,11.76155035,12.43898989,13.08152397,13.68924448\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,8.084645275,8.934425577,9.762936203,10.56585104,11.33932138,12.08019501,12.78615783\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.337015127,10.14027194,10.91467134,11.65688068,12.36454506,13.03622924,13.67131188\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.299997809,10.04649409,10.76136723,11.44615134,12.10152832,12.72768681,13.3246233\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.06364369,10.74831678,11.42736075,12.09472299,12.74389032,13.36927525,13.96674402\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.64984203,11.27074212,11.89464913,12.51430806,13.12221601,13.71192461,14.27853747\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,11.02025266,11.85699283,12.65936546,13.42217485,14.14185093,14.81643548,15.44539898\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.974801922,10.80017722,11.59164464,12.34478689,13.05635051,13.72440572,14.34829666\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,10.91832901,11.75466364,12.5566099,13.31905188,14.03846338,14.71290319,15.3418412\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,9.764172849,10.59089435,11.38366056,12.13796992,12.85052326,13.51937563,14.14387631\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,12.39122326,13.04897226,13.68465331,14.29710292,14.88382628,15.44234752,15.97082918\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,12.09106232,12.73955412,13.35015224,13.92882982,14.47870148,15.00124475,15.49712757\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,12.33453209,12.99331151,13.62991606,14.24318329,14.83062128,15.38975975,15.91876897\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,12.06155588,12.7096703,13.32000199,13.8985374,14.44838687,14.97101277,15.46706293\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,16.05793292,16.74457088,17.35178198,17.89190779,18.37463277,18.8076946,19.19740225\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,15.32429749,16.01911288,16.6511691,17.22840371,17.75657055,18.24015256,18.6829161\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,14.95953169,15.81213873,16.58039542,17.27115194,17.89124503,18.44738611,18.94602236\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,14.93617467,15.71187686,16.41170433,17.04512323,17.61951286,18.1409091,18.61448014\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,16.19203718,16.85631768,17.44257572,17.96415043,18.43157073,18.85308514,19.23517028\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,12.17302414,12.91682026,13.59156872,14.20494051,14.7630092,15.27087511,15.73303895\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,14.69788873,15.49201316,16.21091524,16.86242335,17.45305565,17.98850195,18.47389776\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,13.67215125,14.39491989,15.05251807,15.65162753,16.197578,16.69493488,17.14782313\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,15.62521698,16.28161522,16.86429561,17.38412135,17.84972987,18.26811557,18.64505652\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,15.14406683,15.83970926,16.47254396,17.05051967,17.57940414,18.06368997,18.5071481\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,14.84394768,15.70286295,16.47672805,17.17244994,17.7969329,18.35695612,18.85903003\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,14.87149292,15.64357558,16.34042045,16.9713892,17.54377761,18.06355029,18.53581343\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,14.14980694,14.78488315,15.34758664,15.84992887,16.30147521,16.70976104,17.08072626\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,12.40437187,13.1499805,13.82638784,14.4412093,15.00050097,15.50936958,15.97233531\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,14.55597443,15.35009887,16.06909002,16.72057143,17.31096137,17.84592056,18.33059714\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,13.88511289,14.61432838,15.27698883,15.8802294,16.4296766,16.93008607,17.38570321\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,19.94280627,20.40232628,20.77096239,21.07197914,21.32173075,21.53192324,21.71108091\n\"linker O=C1C=CC(=C[C]1C=[NH]CCCC[NH]=C[C]1C=C(C=CC1=O)S([O])([O])[O])S([O])([O])[O], Oc1ccc(cc1CNCCCCNCc1cc(ccc1O)S([O])([O])[O])S([O])([O])[O], nodes [K][OH2][K], topology \",,,20.0438748,20.49363409,20.853234,21.14605163,21.38844668,21.59207649,21.76539272\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,22.55322383,22.65959162,22.74165856,22.80627685,22.85805138,22.90016675,22.93488075\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,22.60709576,22.7040316,22.77894073,22.83799926,22.88536945,22.92393639,22.9557495\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,22.55325628,22.65961862,22.74168136,22.80629636,22.85806827,22.90018151,22.93489375\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,22.60711527,22.70404772,22.77895427,22.8380108,22.88537939,22.92394505,22.9557571\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.571862704,4.255648959,4.95725161,5.659186855,6.348128163,7.014770267,7.653262233\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.477556989,4.151246048,4.8455528,5.542800943,6.229313361,6.895382604,7.534766069\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.649076356,4.352717424,5.069990516,5.783693633,6.48100011,7.153180365,7.794952068\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.597501503,4.310846268,5.040585049,5.767700145,6.478096562,7.162267262,7.814529061\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.448100669,4.129113552,4.831392763,5.536466467,6.230160082,6.902505592,7.547166535\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.628892713,4.303489705,4.993352421,5.682339631,6.358243363,7.012546936,7.639877727\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.590281657,4.259566339,4.944857562,5.630183454,6.30335737,6.955790965,7.581991274\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.236940384,3.893728721,4.575276521,5.26365168,5.944820343,6.608627578,7.248336435\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.204730613,3.861302978,4.544284926,5.235239374,5.919633759,6.586903673,7.23001172\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.512902124,4.153814936,4.815681957,5.482693397,6.14233662,6.785458313,7.405920079\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.389495817,4.035450641,4.703561582,5.377573591,6.04464076,6.695387211,7.323542532\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,1.732387019,2.17698362,2.686349213,3.249447342,3.854316911,4.489401796,5.144257455\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.738160126,3.26942966,3.827124476,4.4016568,4.984845095,5.570122602,6.152460572\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,8.338390052,9.128996955,9.814418749,10.41108831,10.93379169,11.39499427,11.80486162\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.123070588,2.654365104,3.231098003,3.837654122,4.460562651,5.089005911,5.71477628\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.824807269,3.458761778,4.11464033,4.77698919,5.434072684,6.077505097,6.701708048\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.0051097,2.500061091,3.049954262,3.639886129,4.256132076,4.887054892,5.523332505\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.571828806,4.255608722,4.957206793,5.659138987,6.348078502,7.014719808,7.65321174\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.477561914,4.151244599,4.845546061,5.542789959,6.22929907,6.895365817,7.534747459\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.648657027,4.35217712,5.069340446,5.782950277,6.480182088,7.152306214,7.794038884\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.597228832,4.310492933,5.040157657,5.767209241,6.47755442,7.161686284,7.813920793\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.448112679,4.129120782,4.83139603,5.536466505,6.230157528,6.902500992,7.547160345\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.628887341,4.303483608,4.99334559,5.682332117,6.358235254,7.012538338,7.639868748\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.590259598,4.259538037,4.944823821,5.630145205,6.303315544,6.955746423,7.581944761\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.237056617,3.893852171,4.575404635,5.263782188,5.944951346,6.608757559,7.248464227\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.204769953,3.861346949,4.544332461,5.23528942,5.919685366,6.586956031,7.230064166\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.512749964,4.153655186,4.815517878,5.482527811,6.142171831,6.785296129,7.405761871\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,3.389420482,4.035370361,4.703478381,5.377489157,6.044556424,6.695303983,7.323461149\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,1.732399833,2.176995222,2.68636004,3.249457855,3.85432754,4.489412898,5.144269303\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.738153493,3.269420689,3.827114294,4.401646209,4.984834643,5.570112651,6.152451346\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,8.338365588,9.128968489,9.814388343,10.41105732,10.93376098,11.39496439,11.80483288\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.123075223,2.654374052,3.231110009,3.837668158,4.460577901,5.089021757,5.714792261\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.824841127,3.458803556,4.114688586,4.777042447,5.434129468,6.077563966,6.701767613\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,2.00510686,2.500058657,3.049952007,3.639883901,4.256129776,4.88705246,5.523329909\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.405955789,8.239006962,9.052405901,9.843939524,10.61113211,11.35142951,12.06249774\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,11.313707,12.13516632,12.9028648,13.62143288,14.29439837,14.92455085,15.51423441\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.523263253,10.28812154,11.03217449,11.7514998,12.44260353,13.10282031,13.7304107\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,8.46363892,9.267894768,10.05595625,10.82415874,11.56871932,12.28615522,12.97359759\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.957989958,8.725121701,9.48215603,10.22580147,10.9522919,11.65785767,12.33912065\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.543546019,10.30361267,11.04323045,11.75859926,12.44626163,13.1035396,13.72865579\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.642080255,10.4311857,11.19464293,11.92931105,12.63232223,13.30151406,13.93556316\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.957436819,8.721933387,9.476362643,10.21754689,10.94179568,11.64538447,12.3249558\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.619316586,10.40315276,11.163859,11.89699889,12.59909128,13.26770344,13.90140294\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.936559379,8.708011016,9.470035631,10.21898348,10.9507836,11.66143228,12.3473898\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.873027355,8.770605048,9.64148581,10.48214128,11.28942756,12.06072221,12.79409508\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.859477303,7.651966006,8.437164293,9.209468124,9.964197908,10.69738998,11.40576711\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.41275241,10.19546484,10.95686397,11.69188929,12.39662791,13.06837907,13.70555512\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.157789891,8.021320852,8.87941939,9.722124836,10.54144629,11.33128632,12.08728632\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.542288555,8.321312515,9.085783149,9.831164596,10.55427522,11.25274054,11.92475295\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,10.00392338,10.74378114,11.46055745,12.15157384,12.81448293,13.44746979,14.04933594\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.827388515,7.608642885,8.384007423,9.148700373,9.898327933,10.62885042,11.33670301\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.839719037,8.666763746,9.472115099,10.25458588,11.01212151,11.74231705,12.44289276\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.10167821,7.867196442,8.620694219,9.358883647,10.07909644,10.77891924,11.45614998\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.892521693,8.69807659,9.492332801,10.27069966,11.02845638,11.76129162,12.46564815\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.181398714,8.034518053,8.882483841,9.71582413,10.52682336,11.30950233,12.05951256\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.920672739,7.700933418,8.478663192,9.2472414,10.0010992,10.73549194,11.4464759\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.742121088,8.57258582,9.381357861,10.16729914,10.92836895,11.66214904,12.36633009\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.080608797,7.845147815,8.601565837,9.345067592,10.0718245,10.77859072,11.46260709\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.915908872,10.6630026,11.38485006,12.07940299,12.7448124,13.37963981,13.98295851\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.982747427,7.757095821,8.523489213,9.27672154,10.01269336,10.72799453,11.41978014\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.900323874,7.663915213,8.431825489,9.196053066,9.949641347,10.68662526,11.40206785\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.882439846,8.685694437,9.47817706,10.25523725,11.01209157,11.74436538,12.44844081\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.703628518,10.46928239,11.20890095,11.91980235,12.59997661,13.24802952,13.86315801\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.697059839,10.46701832,11.21017494,11.92422052,12.60727793,13.25797522,13.8754914\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.980938086,10.73498554,11.45816063,12.14951557,12.80860142,13.43525326,14.02954587\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.972940636,10.7423024,11.47854366,12.18102355,12.84949851,13.483965,14.08464589\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.405963735,8.239012772,9.052410071,9.843942504,10.61113427,11.35143113,12.06249903\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,11.31362182,12.13507781,12.9027739,13.62134072,14.29430608,14.92445948,15.51414483\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.523322147,10.28817491,11.03222389,11.75154639,12.44264813,13.10286344,13.7304527\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,8.463529458,9.267743195,10.05576519,10.82393315,11.56846529,12.28587908,12.9733053\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.95799098,8.725124688,9.482161359,10.22580932,10.95230229,11.65787047,12.33913563\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.543621009,10.30367486,11.04328144,11.75864056,12.44629464,13.10356554,13.72867577\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.642132652,10.43122844,11.19467573,11.92933416,12.63233632,13.30152003,13.93556203\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.957455284,8.721952704,9.476382004,10.2175657,10.94181353,11.64540111,12.32497108\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.619256973,10.40308258,11.16377919,11.89691099,12.59899708,13.26760474,13.9013014\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.936532502,8.707973057,9.469988232,10.21892852,10.95072296,11.66136772,12.34732283\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.872966291,8.770511187,9.641362975,10.48199408,11.28926084,12.06054062,12.79390285\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.859476727,7.651959492,8.437152982,9.209453077,9.96418007,10.69737017,11.40574599\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.412810699,10.19551338,10.956904,11.69192198,12.3966543,13.06840009,13.70557159\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.157759071,8.021290514,8.879389884,9.722096349,10.54141891,11.33126007,12.08726119\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.542262149,8.321281649,9.08574701,9.831123072,10.55422865,11.25268952,11.9246982\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,10.00394517,10.74380111,11.46057541,12.15158973,12.81449679,13.44748173,14.04934611\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.827372866,7.608625026,8.383988222,9.148680399,9.898307568,10.62882993,11.33668258\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.839725433,8.666769903,9.472120729,10.25459083,11.01212571,11.74232051,12.4428955\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.101667874,7.867189223,8.620689568,9.358881231,10.07909604,10.77892066,11.45615306\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.892541933,8.698099687,9.492358834,10.27072848,11.0284877,11.76132504,12.46568325\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.181395907,8.034512637,8.882476574,9.71581563,10.52681411,11.30949272,12.05950286\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.920709709,7.700968639,8.478696831,9.247273456,10.00112961,10.73552066,11.44650288\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.742083141,8.572541343,9.38130872,10.16724686,10.92831478,11.66209397,12.3662749\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.080614983,7.845159866,8.601581228,9.345084554,10.07184182,10.77860759,11.46262301\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.915912406,10.6630101,11.38486112,12.07941708,12.74482895,13.37965828,13.98297838\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.982760464,7.757110267,8.523502728,9.276732603,10.01270109,10.72799852,11.41978033\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,6.900338991,7.663931197,8.43184209,9.196070061,9.94965855,10.68664251,11.40208503\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,7.882419491,8.685678852,9.478166078,10.25523051,11.0120886,11.74436567,12.44844386\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.703670801,10.46931836,11.20893196,11.91982937,12.60000036,13.24805051,13.86317667\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.697099223,10.46705488,11.21020906,11.92425248,12.60730797,13.25800351,13.87551809\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.980945472,10.73499197,11.45816478,12.14951675,12.8085994,13.43524809,14.02953778\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,9.973003133,10.74235716,11.47859145,12.18106514,12.84953465,13.48399637,14.08467311\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,14.66314596,15.40542911,16.07518546,16.68242204,17.23494385,17.73903481,18.19990651\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.75532503,16.43619444,17.04116951,17.58284401,18.07115051,18.51391016,18.9173053\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,19.58388741,20.12569985,20.56097036,20.91656328,21.21160527,21.45993115,21.67169891\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.77238131,16.44165925,17.03801799,17.57297606,18.05588128,18.49423053,18.89401646\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,14.97649675,15.71015847,16.37124617,16.96929972,17.51186049,18.00511388,18.45429701\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,14.62493538,15.40735646,16.10748115,16.7373127,17.30611108,17.82127255,18.2889025\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.32806404,16.06068543,16.7077507,17.28384471,17.80053463,18.26694813,18.69029285\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,12.24344874,13.25693265,14.1828276,15.02609463,15.79245827,16.48795393,17.11863719\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.5639102,16.30237799,16.96302961,17.55710985,18.09345164,18.57915379,19.02005663\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.82090151,16.50063494,17.10932509,17.65775643,18.15442864,18.6060875,19.01815731\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.4189664,16.12256267,16.74852809,17.31031066,17.81802096,18.27939504,18.70046562\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.53623125,16.27757546,16.93959378,17.5347528,18.07226931,18.55928409,19.00156897\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,12.16760092,13.20381487,14.15090965,15.01304835,15.79560015,16.50456541,17.14616322\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.79463064,16.43267731,17.01445747,17.54617533,18.03275278,18.47834186,18.88660737\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.91226747,16.55232558,17.12019971,17.62801994,18.0856439,18.50093383,18.88009477\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.13449891,15.90993979,16.5954026,17.20687899,17.75622121,18.25243662,18.70254991\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,16.18456512,16.85630864,17.45938534,18.00376504,18.4970797,18.94538529,19.35364551\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.90730525,16.58829918,17.19955715,17.7511407,18.2509926,18.705484,19.11982049\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.66579968,16.36764594,16.99539567,17.56111461,18.07369564,18.53993553,18.96521772\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,14.66330621,15.40555909,16.0752898,16.68250481,17.23500862,17.73908467,18.19994409\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.75492643,16.43584656,17.04086239,17.58257011,18.07090411,18.51368683,18.91710156\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,19.58439507,20.12613698,20.56134987,20.91689539,21.21189808,21.4601911,21.67193114\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.77217713,16.4414876,17.03787132,17.57284897,18.05576978,18.49413164,18.89392794\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,14.97592746,15.70965344,16.37079464,16.96889336,17.51149271,18.00477939,18.45399149\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,14.62476594,15.40720696,16.10734836,16.73719405,17.30600448,17.8211763,18.28881517\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.32798546,16.06061781,16.70769229,17.28379416,17.80049082,18.26691014,18.69025991\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,12.24321707,13.25672314,14.18263821,15.02592334,15.79230315,16.48781318,17.11850921\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.56412773,16.3025708,16.96320107,17.55726296,18.09358898,18.57927755,19.02016865\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.8212491,16.50092773,17.10957348,17.65796845,18.15461063,18.60624453,19.01829344\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.41899981,16.12259226,16.74855496,17.31033559,17.81804446,18.27941746,18.70048718\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.53636517,16.27769764,16.93970489,17.53485374,18.07236104,18.55936756,19.00164507\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,12.16819746,13.20436553,14.15141657,15.01351423,15.79602802,16.50495837,17.14652437\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.79442639,16.43247767,17.01425921,17.54597725,18.03255493,18.47814491,18.88641227\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.91207859,16.55215305,17.12004041,17.62787153,18.08550469,18.50080253,18.87997045\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.13481417,15.91021962,16.59565197,17.20710214,17.75642175,18.25261757,18.70271382\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,16.18470521,16.85643494,17.45949938,18.00386834,18.49717362,18.94547104,19.35372411\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.90711764,16.58812589,17.19939783,17.75099443,18.25085826,18.70536045,19.11970664\n\"linker OC(=O)C1=CC(=[C]C(=C1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], OC(=O)C1=CC(=[C]C(=C1)Oc1cccc(c1C(=O)[O-])C(=O)[O-])C(=O)O, OC(=O)c1cc(cc(c1)C(=O)O)Oc1cccc(c1C(=O)[O-])C(=O)[O-], nodes [Ba][OH2][Ba], topology pts,\",,,15.66604991,16.36785587,16.99557335,17.56126617,18.07382584,18.54004811,18.96531564\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,19.39115436,19.8450959,20.20515794,20.49496759,20.73132492,20.92638617,21.0890941\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,19.42065668,19.86876659,20.22453203,20.51109908,20.7449565,20.93805368,21.09919248\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.603146986,3.226825516,3.885926004,4.561758301,5.239024627,5.90612448,6.554888165\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,3.691719226,4.376876141,5.075593559,5.771870986,6.453463854,7.11181974,7.741589195\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.889600981,3.580780104,4.301447711,5.030056136,5.75003513,6.449680983,7.121469945\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.582765431,3.134918746,3.727931296,4.346413029,4.97641915,5.606441585,6.227673187\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.702352964,3.252939418,3.843762084,4.459589765,5.086592862,5.713354237,6.331142856\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.787526786,3.47025783,4.184656088,4.90911665,5.626862756,6.325910842,6.998437846\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,3.492005452,4.174935337,4.876375216,5.578885837,6.268998673,6.937212809,7.57748985\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.621396909,3.254468178,3.92087589,4.602019156,5.282844752,5.952044293,6.601730556\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.599786072,3.223505359,3.882703527,4.558667976,5.236086259,5.903348377,6.552278617\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,3.693790082,4.380355487,5.080075563,5.777006034,6.458974457,7.11749673,7.747280647\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.886404018,3.577369851,4.297928879,5.026508936,5.746519093,6.446238719,7.118130648\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.584533123,3.136503114,3.729371531,4.347734227,4.977637554,5.607568084,6.228715529\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.708911453,3.259116615,3.849542982,4.464977133,5.09159973,5.717999281,6.335447548\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.789151187,3.471989822,4.186468057,4.910984489,5.628764809,6.327827807,7.000352928\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,3.49769964,4.180392118,4.881525825,5.583701305,6.273474562,6.941358995,7.581323971\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,2.624602079,3.257838814,3.924368397,4.605592401,5.28646068,5.955668774,6.605333982\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.025101876,9.824016896,10.59420716,11.33391561,12.04131313,12.7148899,13.35366578\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.041281541,9.82391743,10.57857714,11.30308142,11.99569901,12.65523557,13.28105187\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,7.909407681,8.624349972,9.334177049,10.03633964,10.72704647,11.40213912,12.05770279\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.397461355,10.19491566,10.95838303,11.68720472,12.38067801,13.03832873,13.66005396\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,8.851321077,9.615077186,10.35401186,11.06724772,11.75322688,12.41031205,13.03715545\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,6.650416173,7.427226156,8.199037438,8.959711253,9.70427673,10.4286054,11.12930891\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,8.968435432,9.717255234,10.44598256,11.15245696,11.8340609,12.48833599,13.11333036\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.389160945,10.20074099,10.97655853,11.71584647,12.41795397,13.08254553,13.70969843\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,7.883516201,8.607477654,9.325366564,10.03462003,10.73146897,11.41180111,12.07176456\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.077216431,9.857113401,10.60804171,11.32848855,12.01711293,12.67293084,13.29540115\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,8.959039461,9.768108941,10.54773935,11.29594557,12.01082207,12.69087476,13.33519015\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,6.521912475,7.300685932,8.07706193,8.844296867,9.596840162,10.33003596,11.04004304\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.029561342,9.829038378,10.59965924,11.33967021,12.04725856,12.72093382,13.35973422\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.042871871,9.825746583,10.58066688,11.30540596,11.99821353,12.65789062,13.28380037\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,7.899033686,8.614517676,9.324849453,10.02745058,10.71853172,11.39394715,12.04979631\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.401978025,10.19927264,10.96248946,11.6910098,12.3841613,13.04149057,13.66290762\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,8.859579477,9.622442297,10.36058956,11.07311889,11.75846006,12.41496936,13.04129491\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,6.705576358,7.474898105,8.240450404,8.995793304,9.735777297,10.45615439,11.15344609\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,8.976521289,9.724063719,10.45168117,11.15720287,11.83799565,12.49158422,13.11600033\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.389635606,10.20138567,10.9772274,11.71646199,12.41847925,13.08296722,13.71001636\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,7.871260519,8.596294601,9.315010162,10.02493088,10.72234334,11.40317019,12.06358098\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.074024388,9.854446483,10.60575393,11.32648914,12.01534323,12.67135102,13.29398254\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,8.97159968,9.780560307,10.5599457,11.30782042,12.02231161,12.70194719,13.34582892\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,6.515515336,7.295176084,8.072056326,8.839544371,9.592185586,10.32539132,11.03536562\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.864931142,10.67823471,11.45881694,12.20575478,12.91767417,13.59336043,14.23206719\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,10.058204,10.85971131,11.63026837,12.36856341,13.07287665,13.74171568,14.3741269\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,9.853889615,10.66676896,11.44705959,12.19382334,12.90567525,13.58138911,14.22020574\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,10.04531509,10.84767344,11.61903452,12.3580769,13.06308039,13.73255563,14.36555318\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,12.97459572,13.94075575,14.80546095,15.58046852,16.27624564,16.90198814,17.46573739\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,14.98668492,15.70798842,16.34493296,16.91278878,17.42313311,17.88482718,18.30473473\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,14.20007954,15.03991172,15.78758173,16.45637649,17.05706218,17.5984307,18.08774857\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,14.31422132,15.12707663,15.84417775,16.48199972,17.05328889,17.56796815,18.03385119\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,13.05964187,14.01370224,14.86894394,15.63639689,16.32602182,16.94666237,17.50611286\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,15.58934542,16.23341657,16.80720388,17.32277003,17.78932489,18.21396412,18.60221896\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,14.09134411,14.94289715,15.70092579,16.37878388,16.98736551,17.5356068,18.03091383\n\"linker [O-]C(=O)c1ccncc1, nodes [Cu], topology kgm,pcu\",,,14.21404212,15.03846624,15.76545812,16.41172129,16.99022875,17.51110529,17.98233596\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,19.99353765,20.50377397,20.90997868,21.2378849,21.5059399,21.72758084,21.91274674\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,19.93567319,20.45378916,20.86650913,21.19982376,21.47239456,21.69783106,21.88620913\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,20.1106455,20.60257872,20.99435372,21.31070865,21.56938823,21.78332482,21.96208859\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,19.99215534,20.50259276,20.90896003,21.23699889,21.50516318,21.72689499,21.91213715\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,19.93581601,20.45391022,20.86661285,21.19991348,21.47247286,21.69789994,21.88627016\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,20.111528,20.60332735,20.99499565,21.31126445,21.56987368,21.78375216,21.96246746\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,3.345937705,4.029610208,4.730135399,5.430821148,6.118965575,6.785649768,7.425196246\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,3.341681893,4.02522524,4.725682061,5.426358505,6.114544526,6.781310766,7.420969379\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,3.365301017,4.051255214,4.753313461,5.454879662,6.143373616,6.809996827,7.449178152\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,3.345992772,4.029673424,4.730204812,5.430894885,6.11904199,6.785727492,7.425274186\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,3.341786529,4.025359912,4.725841198,5.426536432,6.114736011,6.781511265,7.421175106\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,3.365271115,4.051233738,4.753300256,5.454874121,6.143374883,6.810003943,7.449190158\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,6.694424471,7.509160044,8.314559431,9.105682469,9.878126065,10.62793322,11.35170019\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.796854373,8.603939184,9.4004653,10.18155584,10.94215733,11.67767601,12.38435315\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.434038193,8.29852096,9.142807509,9.963343347,10.75657438,11.51923481,12.24864016\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,9.285329592,10.10552784,10.89234775,11.64343426,12.35737896,13.03351423,13.67178699\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,6.700483481,7.513630012,8.317750842,9.107871119,9.879543019,10.62876524,11.35209472\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.794782437,8.60182322,9.398462273,10.17976222,10.9406234,11.67641947,12.38337027\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.422673166,8.287759781,9.13280411,9.954159249,10.74821228,11.51166212,12.24180491\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,9.273986065,10.09536919,10.88321658,11.6352053,12.34994735,13.02678962,13.66569036\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,6.707129849,7.521641788,8.326683403,9.117383035,9.889375666,10.63872493,11.36203806\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.797584343,8.605419536,9.402557026,10.18414965,10.94516047,11.68100659,12.38793813\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.430319295,8.295696745,9.140705638,9.961829115,10.75553982,11.51859185,12.24831619\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,9.293189235,10.11458267,10.90216284,11.65367046,12.3677794,13.04388982,13.68200254\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,6.694448516,7.509182123,8.314579984,9.10570191,9.878144747,10.62795141,11.35171809\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.796849501,8.603937123,9.400465375,10.18155746,10.94216,11.67767934,12.38435686\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.434029005,8.298513575,9.142802748,9.96334157,10.75657563,11.5192389,12.24864683\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,9.285372396,10.10557042,10.89238985,11.64347564,12.35741939,13.03355353,13.67182503\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,6.700517088,7.513663997,8.317784998,9.107905289,9.879577067,10.62879904,11.35212815\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.794814304,8.601859707,9.398503135,10.17980685,10.94067102,11.67646927,12.3834215\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.422591442,8.287680016,9.132726949,9.954085084,10.74814133,11.5115945,12.24174063\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,9.273977405,10.09537781,10.88323943,11.63523964,12.34999078,13.02684009,13.6657461\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,6.7071658,7.521672385,8.326707642,9.117400585,9.88938668,10.63872987,11.36203756\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.797555756,8.605397836,9.402541553,10.18413952,10.94515475,11.6810044,12.38793869\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,7.430346918,8.295723268,9.140732058,9.96185604,10.75556756,11.51862048,12.24834564\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,9.293206355,10.11460379,10.90218698,11.65369683,12.36780736,13.04391884,13.68203219\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.65427397,15.44636207,16.15330824,16.78719424,17.35800275,17.87393574,18.34175619\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.94303536,14.78758637,15.55391237,16.24910226,16.87983461,17.45228666,17.97211748\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.95062247,14.98747238,15.89585729,16.69343281,17.39565353,18.01577523,18.56507291\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.66605595,15.45671756,16.16258706,16.79564386,17.36579605,17.88119319,18.34856224\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.05687115,14.8937199,15.65204278,16.33941767,16.9627769,17.52841156,18.0420143\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.11300502,15.13430553,16.02823511,16.81272227,17.50326346,18.11304287,18.6532151\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.66275327,15.45523304,16.16228973,16.79611075,17.36674484,17.88243579,18.34997357\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.85096064,14.70623271,15.48156709,16.18440928,16.8216984,17.39980878,17.92455259\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.8825358,14.92621266,15.84079895,16.64390805,17.35101999,17.97544582,18.52852564\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.6543617,15.44643325,16.15336807,16.78724616,17.35804905,17.87397797,18.34179536\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.94298585,14.78754791,15.5538808,16.24907499,16.87981006,17.45226385,17.97209585\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.95071636,14.98756171,15.89594142,16.69351159,17.39572707,18.01584376,18.56513674\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.66629317,15.45692803,16.16277352,16.79580908,17.36594265,17.88132354,18.34867846\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.05677781,14.89364379,15.65197815,16.33936092,16.96272579,17.52836469,18.04197077\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.11296815,15.13425958,16.02818207,16.81266397,17.50320153,18.11297869,18.65314978\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,14.66271616,15.45520449,16.16226852,16.79609592,17.36673554,17.88243125,18.3499731\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.85131812,14.70656331,15.48186726,16.18467843,16.82193768,17.4000203,17.92473888\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Ni], topology pcu\",,,13.88269764,14.92634858,15.84091337,16.64400471,17.35110199,17.97551572,18.52858552\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,20.17847123,20.34002284,20.46695502,20.56838759,20.65065238,20.7182487,20.7744399\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,20.1779245,20.33954739,20.46653933,20.56802212,20.65032928,20.71796153,20.77418336\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,20.12761134,20.29441065,20.42625553,20.53211569,20.61829585,20.68932206,20.7485053\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,3.306785026,3.970527748,4.656673482,5.347861478,6.030452173,6.694593244,7.333797402\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,3.39042471,4.05600118,4.743444321,5.435284677,6.117875121,6.781422345,7.419534551\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,3.301985846,3.952833388,4.627271142,5.308197601,5.982120742,6.639219919,7.272946314\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,3.313429652,3.977511517,4.663864748,5.355146605,6.037737247,6.701803411,7.340875007\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,3.387501938,4.052011298,4.738547889,5.429654442,6.111676155,6.774800563,7.412611589\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,3.289546326,3.93931976,4.613012906,5.293493861,5.96722845,6.624351835,7.258274117\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,7.171710617,8.005959213,8.833080349,9.645470898,10.43654051,11.20090135,11.93444586\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,7.567339309,8.358688811,9.139806687,9.906550738,10.65449836,11.3794643,12.07787248\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,9.079920464,9.881388818,10.65648745,11.40106467,12.11222974,12.78818841,13.42807037\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,7.859064731,8.612400081,9.357159123,10.09039226,10.80823126,11.50663511,12.18192348\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,9.418947491,10.19912998,10.95036495,11.67075065,12.3586954,13.01306816,13.63326604\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,9.58752144,10.37750398,11.13258883,11.852455,12.53688334,13.18581208,13.79941926\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,6.625531259,7.411739711,8.193894363,8.965468063,9.721189848,10.45666249,11.16825367\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,6.558407803,7.338473878,8.11635924,8.885685154,9.640977055,10.37748799,11.09121133\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,6.626646907,7.397610296,8.170763742,8.938572744,9.694548904,10.43311022,11.14960246\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,7.176178104,8.010547432,8.837668746,9.649966008,10.44087563,11.20503301,11.93834914\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,7.566963877,8.358583533,9.139979255,9.907003541,10.65522533,11.38045089,12.07909729\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,9.080238382,9.881595545,10.65667019,11.40128288,12.11252028,12.7885709,13.428552\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,7.861351608,8.614906866,9.359815655,10.09313115,10.81099412,11.50937487,12.18460442\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,9.420196429,10.19919748,10.9494044,11.6689099,12.35611405,13.00987513,13.62957792\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,9.58819118,10.37737294,11.13162006,11.85066269,12.53431966,13.18255392,13.79555696\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,6.624212856,7.410268235,8.192417066,8.964091534,9.719985187,10.45567184,11.16749686\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,6.557399627,7.337528633,8.115659315,8.885377062,9.641162502,10.37822426,11.09251716\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,6.630645982,7.40194604,8.175382303,8.943413024,9.699549438,10.43821329,11.15475632\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.58884595,16.27715633,16.88886869,17.43725833,17.93219217,18.38117659,18.79006654\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.33281371,16.02525938,16.65084401,17.21776286,17.73292261,18.2021322,18.63030893\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,14.42880467,15.24707656,15.98049044,16.63994028,17.23450433,17.77181662,18.25836689\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.59155245,16.26758567,16.87027479,17.41196592,17.90191447,18.3472144,18.75343222\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,14.670466,15.43221956,16.12214636,16.74731118,17.31439767,17.82946974,18.29792899\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.65704401,16.33908457,16.95005353,17.50102733,18.00028577,18.45424345,18.86804708\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.59621507,16.28480028,16.8969884,17.44594574,17.94145959,18.39098281,18.800338\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.34503457,16.03478804,16.65799381,17.22281731,17.73614732,18.20377704,18.63060642\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,14.43456614,15.2519059,15.98442589,16.64304249,17.23684886,17.7734867,18.25944749\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.58524091,16.2634141,16.86808571,17.41158144,17.90314106,18.34985099,18.75727862\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,14.6715079,15.43237612,16.12139892,16.74569373,17.31198088,17.82634622,18.29420127\n\"linker [O-]C(=O)c1cc(ccc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology ths\",,,15.6679971,16.34926976,16.9597638,17.51044545,18.00951758,18.46334273,18.87703387\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,18.75950733,19.22665758,19.60884634,19.92450226,20.18754836,20.40860295,20.59583796\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,18.46513878,18.96311349,19.3708001,19.70773054,19.98866789,20.22487981,20.42504548\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,16.69718204,17.30480083,17.80546493,18.22114391,18.56890087,18.86200938,19.11083531\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,1.752135403,2.207406982,2.723403426,3.286051639,3.881156283,4.495937918,5.119737855\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.807193542,3.346744995,3.920606052,4.516330378,5.122377711,5.728998007,6.32855715\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.645327348,3.134216835,3.65633549,4.204078784,4.769326663,5.344431599,5.922776175\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.202879493,3.677672554,4.1858815,4.718853344,5.267217274,5.822184775,6.376270086\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.175219907,3.66303781,4.188305241,4.739390184,5.305025632,5.875369504,6.442467329\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,1.763415352,2.219220159,2.735109432,3.297020469,3.890838595,4.503895264,5.125647206\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.818017029,3.352653837,3.921599435,4.512700466,5.114589255,5.717591051,6.314079676\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.687138953,3.176694116,3.698668962,4.245539479,4.809275733,5.382317945,5.958131758\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.198038358,3.676694984,4.188469122,4.724497478,5.275309486,5.832100944,6.387426398\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.16806317,3.657810379,4.184516258,4.736536804,5.302637639,5.873028135,6.439810382\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,1.761707628,2.216585356,2.732126396,3.294322032,3.889019364,4.503462873,5.127003996\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.819677539,3.358935519,3.932486568,4.527902314,5.133654216,5.739999187,6.339306636\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.666437585,3.155731308,3.678113199,4.225988659,4.791251874,5.366272195,5.944449858\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.218374939,3.693438985,4.201931315,4.735153058,5.283702103,5.838773172,6.392875426\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.187629303,3.675153617,4.20024254,4.751218433,5.316779894,5.887061066,6.454092491\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,1.76278684,2.218801398,2.734870674,3.296914845,3.890806265,4.503867831,5.125552428\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.817120356,3.352116307,3.921420658,4.512850861,5.115026304,5.718268981,6.314954743\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,2.681997382,3.171889079,3.694231561,4.241446685,4.805473523,5.378736229,5.954694268\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.188616369,3.667917823,4.18036782,4.717060573,5.26850277,5.825879533,6.381741788\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,3.164064531,3.654350104,4.181559885,4.734038331,5.300547431,5.871297722,6.438395068\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,6.868022912,7.670720957,8.48610497,9.300682996,10.10238683,10.88147505,11.63074251\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,9.148575524,9.909642764,10.65155784,11.37071436,12.06307527,12.72516083,13.3544783\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,9.518873689,10.29340932,11.04744858,11.77524382,12.47184601,13.13366122,13.75854125\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,5.913414162,6.720595759,7.527847077,8.32661456,9.110034328,9.872526079,10.60964319\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,6.722737402,7.513381706,8.318660374,9.124320971,9.91796359,10.68972584,11.43236759\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,8.917771109,9.669119054,10.40251173,11.11406831,11.79960378,12.45554898,13.07934694\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,9.209520396,9.975628578,10.72222243,11.44341866,12.13417999,12.79083863,13.41117656\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,6.143183912,6.891832188,7.647584279,8.402344812,9.149098154,9.881741744,10.59511106\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,7.017721736,7.819955853,8.634778398,9.448780541,10.24994194,11.02854477,11.77739228\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,9.25148662,10.01214613,10.75364196,11.47237656,12.1643226,12.82600839,13.45494689\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,9.577513271,10.35018924,11.10260408,11.8289772,12.52433089,13.18504626,13.8089537\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,6.148354013,6.963638428,7.777081895,8.580560772,9.367553779,10.13275425,10.87193189\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,6.720390605,7.512839193,8.319812196,9.127003397,9.922002844,10.69495773,11.43864494\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,8.928755512,9.679888154,10.41317459,11.12468641,11.81021042,12.46616078,13.08997073\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,9.20750398,9.974034465,10.72107328,11.44271509,12.13391198,12.79099102,13.41173162\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,6.097951305,6.8476228,7.604523887,8.36047243,9.10843659,9.842323559,10.55698223\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,13.66031461,14.50489494,15.25826325,15.93279097,16.5388658,17.08517406,17.57899824\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,12.87818948,13.72724272,14.49458941,15.18915303,15.81876423,16.39029188,16.90977384\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,13.81938675,14.66789873,15.42082161,16.09266939,16.69511018,17.23757564,17.72776389\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,13.95155299,14.76983274,15.5043099,16.16561959,16.76253808,17.30245622,17.79169574\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,13.93012239,14.77269343,15.52557006,16.20063406,16.80792243,17.3558752,17.85160355\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,12.8551413,13.75965984,14.57573036,15.31325821,15.98089412,16.58619262,17.13576694\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,13.80307523,14.63931873,15.38522972,16.05348513,16.65451243,17.19692152,17.68787277\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,13.96255658,14.77555956,15.50676129,16.16621258,16.76226322,17.30200128,17.79153553\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,15.20474006,16.14850015,16.96298184,17.66494338,18.27033656,18.79350838,19.2469437\n\"linker [O-]C(=O)C1CCC(CC1)C(=O)[O-], nodes [Ni]O[Ni]O[Ni], topology sql\",,,15.91650421,16.82865485,17.61644552,18.2958912,18.88225205,19.3892755,19.82894472\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,20.77627218,21.05489444,21.27534836,21.4525224,21.59688915,21.71597254,21.8152808\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,20.81694672,21.08985183,21.3056704,21.47903841,21.62024626,21.7366829,21.8337546\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,2.481048063,3.11916107,3.798487231,4.498393436,5.201563564,5.894707664,6.56844553\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,2.026566983,2.607343201,3.241059428,3.907356105,4.588180003,5.268934167,5.938693075\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,4.573017877,5.323495568,6.063935521,6.781504042,7.467759952,8.117833274,8.729605979\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,4.281027,5.041968521,5.796674606,6.530621681,7.234116308,7.901439504,8.529941974\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.372514284,8.214744782,9.034268103,9.827388948,10.59154954,11.32483588,12.02583231\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.149186347,7.976802479,8.787355856,9.577441289,10.34391019,11.08385259,11.79475403\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,6.813639151,7.640894793,8.457226795,9.257123692,10.03594365,10.78971366,11.51516363\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,6.906828079,7.746280441,8.571949432,9.378632264,10.16200103,10.91840167,11.64487658\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,6.982155532,7.815447873,8.631763618,9.427186436,10.19845297,10.94272088,11.65760263\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.502834732,8.33842002,9.151481641,9.938641396,10.69741081,11.42583159,12.12240459\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,6.820926712,7.651347222,8.471304593,9.27498964,10.05749596,10.81465587,11.54307848\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,6.832385784,7.660584311,8.474263269,9.269100494,10.0414703,10.78819369,11.50657488\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.308416159,8.342122589,9.365517557,10.35679789,11.30125079,12.19012841,13.01925383\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.128779035,7.959101609,8.790762673,9.612029728,10.41365071,11.18863556,11.93199062\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.899836151,8.933312598,9.936087674,10.89433974,11.79925997,12.64617722,13.43355872\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.202491042,8.246334228,9.276151572,10.27247358,11.22246737,12.11854521,12.95703558\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,9.638150941,10.37205215,11.09336082,11.79599428,12.4747181,13.12549393,13.74553329\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,7.986042194,8.916053179,9.822321413,10.69624151,11.53171214,12.32476539,13.07320373\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,9.505428173,10.2659365,11.00746424,11.72566917,12.41652705,13.07685645,13.70448737\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,8.049484259,8.978920949,9.884310949,10.75715511,11.59139567,12.38308456,13.13003912\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,19.65846195,20.23208472,20.7014509,21.08866803,21.41076599,21.68087041,21.90913734\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,17.77231844,18.56731564,19.22732156,19.7782107,20.24086714,20.63194634,20.96467653\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,17.29931363,18.08231408,18.74594841,19.31024694,19.79205785,20.20533115,20.56152443\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,17.35707334,18.12109079,18.77106756,19.32553876,19.80028081,20.20847752,20.56103819\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,11.00064102,11.82459814,12.6049697,13.34255294,14.0377079,14.69082317,15.30256909\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,10.83569727,11.70661154,12.52182832,13.28488324,13.99838546,14.66452294,15.2853698\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,10.22707433,11.15676771,12.03528149,12.86197776,13.63655642,14.35938951,15.03158858\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,10.28894894,11.21818427,12.09702131,12.92447759,13.69992945,14.4235129,15.0961959\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,10.61252609,11.51911042,12.36637083,13.15777502,13.89604758,14.58359616,15.22277565\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,11.10520628,11.89077579,12.637005,13.34471585,14.01417436,14.6455705,15.23929079\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,10.19655875,11.138301,12.02879853,12.86669457,13.65126294,14.38267987,15.06202266\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,10.42899038,11.32887374,12.18078903,12.98428952,13.7389466,14.44484753,15.10275699\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,14.82759223,15.59322616,16.26682857,16.86429332,17.39829419,17.87881965,18.31372577\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,14.35573541,15.20767729,15.95867244,16.62457052,17.21840999,17.75074348,18.2300922\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,14.37521837,15.25779521,16.03226273,16.71586599,17.32272826,17.86428309,18.34978456\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,13.85746914,14.78176091,15.59370599,16.31089135,16.9478694,17.51650064,18.02642596\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,14.85870316,15.63978497,16.32851578,16.9406498,17.48853403,17.98181183,18.42806662\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,14.18562072,15.04135528,15.79226897,16.45543579,17.04501536,17.57248479,18.04705986\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,14.23931792,15.14500462,15.93798683,16.63649842,17.25544805,17.80687562,18.30049959\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, O=C1[N]C2=NC(=O)C12, [S]SC1=NC(=O)[CH]C(=O)[N]1, nodes [Zn], topology cpr,pcu\",,,13.84592663,14.76508209,15.57409397,16.28968765,16.92588227,17.49421776,18.00414557\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,22.0630403,22.21175764,22.32719495,22.41853474,22.49201273,22.55197939,22.60154218\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,22.06400799,22.21219642,22.32732287,22.41847911,22.4918496,22.55175503,22.60128511\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,22.06627633,22.21407484,22.32890726,22.41983536,22.49302474,22.55278366,22.60219334\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,22.06232572,22.21114907,22.32667152,22.41808056,22.49161546,22.55162935,22.60123167\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,2.969801915,3.593780626,4.245247004,4.907950851,5.568727766,6.217672132,6.847871497\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.648923783,4.32773854,5.024469402,5.722062584,6.407245507,7.070623906,7.706226406\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.022526718,3.700532778,4.407336326,5.122498722,5.830080287,6.518673781,7.180838213\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.057792886,3.621203486,4.216130798,4.82896865,5.447633529,6.062304243,6.665579473\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.134187043,3.734253438,4.362845667,5.005081778,5.648234665,6.282317445,6.900090629\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.266891477,3.942556123,4.642459429,5.34789068,6.044191358,6.720857499,7.371058971\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.485962858,4.160265256,4.855830527,5.554952642,6.243715356,6.912156825,7.553839466\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.271913888,3.899075969,4.548330059,5.20508166,5.857349533,6.49605099,7.114840366\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,2.967258471,3.591148961,4.242520567,4.905131263,5.565824479,6.214699429,6.844845289\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.65353952,4.332286795,5.028941699,5.726445349,6.41152544,7.074790144,7.710271019\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.022895832,3.701696686,4.409209924,5.124964791,5.833015292,6.521962043,7.18437836\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.081832098,3.648095433,4.245241849,4.859642196,5.479246221,6.094292814,6.697449445\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.146137935,3.745486282,4.373308397,5.014775533,5.657189679,6.290577867,6.907705663\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.239592416,3.915807396,4.61664291,5.323229636,6.020797803,6.698768332,7.350262119\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.500954265,4.175618427,4.871239749,5.570188869,6.258614091,6.926605284,7.567764991\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.249619596,3.878167442,4.528980787,5.187329115,5.841148158,6.481309167,7.101444829\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,2.964590098,3.589086436,4.24093163,4.903910163,5.564888739,6.213985414,6.844304078\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.64279822,4.322681398,5.020347421,5.718744543,6.404611199,7.068567203,7.704655466\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.023232322,3.702807467,4.410906281,5.127087324,5.835434673,6.524576126,7.187108053\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.075609467,3.642557224,4.240314802,4.855256085,5.475336516,6.090801393,6.694324512\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.136880333,3.737255542,4.366156163,5.008675714,5.652070671,6.286345529,6.904258444\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.263750823,3.939295485,4.639185027,5.344668503,6.041060665,6.717840151,7.368165641\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.491239502,4.165318675,4.860665635,5.559570685,6.248116849,6.916343242,7.557814025\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.272313687,3.900063346,4.549819993,5.20697737,5.859556003,6.498482203,7.117422473\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,2.971307709,3.595018959,4.24622267,4.908681144,5.569236941,6.217987357,6.848020162\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.651818405,4.330522629,5.027129602,5.724590352,6.409636853,7.072878616,7.70834714\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.025506948,3.70320338,4.409698269,5.124570425,5.831888534,6.520248134,7.182207844\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.06331237,3.627265683,4.222601317,4.835717885,5.454545402,6.069279865,6.672537713\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.139106423,3.737783994,4.365059673,5.006107311,5.648225513,6.281432584,6.898481638\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.250009724,3.925712114,4.625967422,5.331951453,6.028923593,6.706322444,7.357278739\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.498095581,4.172549494,4.868056897,5.566968893,6.255414752,6.923467966,7.564717824\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,3.255737483,3.883348301,4.533240134,5.190736484,5.843799037,6.483307171,7.102891103\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.353874605,10.12737885,10.87944812,11.60637999,12.30490128,12.97244215,13.60724927\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.365542844,10.1316275,10.87283721,11.58672664,12.27116589,12.92453686,13.54580725\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.305183725,9.005284112,9.701813988,10.3923648,11.07309263,11.73969002,12.38805588\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.531157051,10.32264295,11.08385199,11.81301539,12.50863026,13.1696469,13.79554843\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.30601618,10.03064281,10.74092884,11.43323358,12.10390099,12.74973758,13.36825889\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.729504971,7.512335415,8.291688015,9.06118098,9.815531438,10.55027623,11.26170589\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.185300832,9.935070133,10.66865169,11.38203959,12.07143685,12.73365079,13.36628924\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.381661857,10.17308529,10.93503502,11.66569344,12.36349463,13.02730816,13.65652398\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.329036359,9.01949779,9.708499918,10.39328408,11.06966181,11.7330271,12.37903402\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.352098318,10.1286897,10.87783331,11.59774099,12.28677208,12.94365893,13.56761807\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.140661347,9.910612492,10.66200028,11.39054319,12.09247747,12.76481295,13.40543719\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.710820434,7.483238974,8.255370573,9.020174669,9.771801676,10.50531143,11.21660352\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.349180981,10.12324144,10.87607016,11.60387168,12.3033039,12.97174691,13.60741257\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.3780498,10.14623227,10.88959161,11.60552662,12.29181341,12.94678339,13.56938363\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.311216549,9.011944011,9.709295465,10.40076845,11.08244251,11.74995159,12.39915326\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.539782497,10.33367908,11.0971571,11.82833781,12.52566633,13.18807983,13.81507225\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.309450929,10.03487357,10.74623606,11.43975466,12.11166607,12.75869963,13.37831859\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.727674221,7.51296827,8.294249873,9.065255291,9.820784789,10.55643678,11.26854987\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.211114554,9.958212465,10.68948748,11.40087738,12.08853912,12.74924102,13.38055768\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.396148525,10.18956834,10.95299571,11.68469865,12.38318783,13.04739811,13.67677448\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.331607983,9.02282395,9.712388382,10.39756732,11.07420534,11.73772674,12.38381025\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.333034916,10.10985147,10.85941959,11.57986058,12.26948436,12.92699502,13.55159195\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.13447479,9.90749511,10.66151603,11.39224784,12.09595853,12.76970527,13.41142674\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.73221231,7.499900908,8.268607158,9.030909718,9.780699693,10.51285438,11.22314206\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.319510148,10.09686701,10.8525556,11.5828229,12.28438006,12.95465875,13.59191644\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.353805785,10.12494627,10.87085252,11.58897023,12.27712687,12.93370148,13.5576826\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.300663706,9.002279594,9.700403005,10.39254344,11.0747968,11.74281297,12.39246321\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.505495756,10.30329405,11.07007153,11.80403696,12.50372435,13.16814913,13.79687008\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.290465766,10.01820331,10.73154629,11.42674804,12.10008881,12.74833915,13.36899827\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.724350873,7.509962092,8.291459511,9.062617269,9.818261356,10.55400678,11.26620233\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.197901165,9.947164669,10.68035809,11.39342872,12.08254767,12.74450092,13.3768829\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.401883207,10.19205924,10.95292381,11.68263114,12.37958864,13.04264256,13.67116387\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.331242076,9.021931292,9.711226807,10.39631513,11.07297745,11.73659174,12.38280471\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.363432557,10.13834114,10.8861128,11.60489154,12.29298676,12.94909274,13.57239648\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.13888201,9.909040831,10.66069859,11.38952665,12.0917359,12.76432316,13.40517032\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.710376355,7.482465057,8.254742225,9.019953961,9.77211183,10.50618815,11.21802979\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.357788199,10.1308364,10.8824988,11.60906762,12.3072664,12.97452237,13.60907916\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.376330365,10.14160018,10.88203234,11.59519115,12.27895224,12.9316994,13.55239963\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.313754589,9.012528512,9.707934638,10.39753143,11.07744889,11.74335805,12.39113964\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.538616559,10.32941284,11.08991041,11.81838458,12.5133572,13.17379023,13.79917026\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.307792084,10.03251573,10.74288299,11.43524463,12.10594403,12.75179043,13.37030317\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.762013262,7.540328527,8.315981743,9.0824133,9.834211268,10.56681445,11.27643671\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.206412877,9.953872798,10.68544757,11.39708215,12.08494305,12.7458085,13.37726206\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.400956286,10.19224033,10.95396349,11.68430514,12.38170824,13.04505621,13.67375407\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,8.336813921,9.026695525,9.715157942,10.39944683,11.07537347,11.73832928,12.38396472\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.324028727,10.10139604,10.85146532,11.5723923,12.26249303,12.92046791,13.54551066\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,9.132374354,9.90438748,10.65754658,11.38758506,12.09076439,12.76412357,13.40557982\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,6.70615364,7.478950415,8.251449368,9.016595919,9.768534121,10.5023224,11.21386179\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.03701653,11.78198393,12.50363909,13.19905874,13.86533913,14.500125,15.1018281\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.39390168,12.10688507,12.80190115,13.47485998,14.12190385,14.7399398,15.3268276\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.06968679,11.81620832,12.5391144,13.23536761,13.90204951,14.53684297,15.13822072\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.43697108,12.1476642,12.8403858,13.51106243,14.15587043,14.77174887,15.35658119\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.06096653,11.80814536,12.53169721,13.22856266,13.8958131,14.53112781,15.13297964\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.42767487,12.13900121,12.83237019,13.50369185,14.14912457,14.765594,15.35097548\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.04021497,11.7847799,12.5061002,13.20123406,13.86726709,14.50183738,15.10335199\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,11.41493149,12.12464738,12.81695624,13.48765953,14.13281779,14.74927366,15.33483469\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.60672736,14.53487834,15.35661776,16.08804912,16.7423525,17.3302579,17.86053041\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,14.3250605,15.18557145,15.94544815,16.62151785,17.22681953,17.77155446,18.26382586\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,14.47400802,15.31848098,16.06629973,16.73276408,17.33001557,17.8677353,18.35372684\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.6493196,14.57585154,15.39764265,16.12996043,16.78546265,17.37456421,17.90585232\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.61811461,14.54592679,15.36705267,16.09772919,16.7512252,17.33832631,17.86783028\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.90144873,14.80909066,15.61026172,16.32225179,16.95872189,17.53050807,18.04629966\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,14.15990574,15.04080843,15.81948633,16.51214321,17.13173428,17.68862402,18.19117294\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,14.61568032,15.43773676,16.1693871,16.82382762,17.41185293,17.942271,18.42231201\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.62671491,14.55475059,15.37582186,16.10627533,16.75945192,17.34618343,17.87529672\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.82444252,14.74119647,15.55018092,16.2688479,16.91102825,17.48771274,18.00772373\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,14.59015778,15.42315324,16.1601164,16.81665447,17.40500995,17.93485179,18.41391457\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.97923167,14.86807126,15.65728497,16.36148327,16.99269767,17.56078044,18.07382889\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.72945768,14.64738159,15.45979201,16.18276483,16.82942769,17.41044483,17.93451107\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,14.58100833,15.41338486,16.149007,16.80413989,17.39131758,17.92030692,18.39884478\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,14.45818219,15.30689085,16.0579559,16.72693103,17.32613678,17.8653834,18.35256968\n\"linker [O-]C(=O)c1ccncc1, nodes [Cd], topology acs\",,,13.68292061,14.60278386,15.41916078,16.14708646,16.79902386,17.38522947,17.91416294\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,15.64211362,15.79340877,15.91284706,16.00863635,16.08653658,16.15067715,16.20407531\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,15.34002654,15.90578052,16.3729521,16.7608351,17.08497629,17.35771692,17.58880054\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,3.040989452,3.558931565,4.096164736,4.645554114,5.200196526,5.753928666,6.301635477\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.79412435,3.246675391,3.740301388,4.266643155,4.816335044,5.380398713,5.951008772\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.963375691,3.478883794,4.026324661,4.595603226,5.176820735,5.761245975,6.341779574\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.96778716,3.457651436,3.983155553,4.535221062,5.104468767,5.682330141,6.261612874\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,3.906552785,4.445009277,4.996764171,5.553564999,6.107949838,6.653573633,7.185343851\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.688270693,3.13730941,3.62629854,4.146567497,4.688508789,5.242893721,5.801654355\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.639455012,3.123079057,3.646401104,4.199890343,4.773705847,5.358827514,5.94762912\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,3.195249764,3.701406288,4.23734365,4.793881152,5.361617688,5.932023376,6.498021582\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,3.967657781,4.51097955,5.062719917,5.616415213,6.166157552,6.706932946,7.234799518\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.515400491,2.967252722,3.463378402,3.994833529,4.551966122,5.125631743,5.707854449\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,3.038569488,3.55520592,4.103233001,4.672495064,5.252900919,5.835494066,6.412975823\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.937345084,3.437656767,3.973019646,4.5339078,5.110744214,5.694932814,6.279356611\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.874191452,3.36591486,3.879462322,4.408855205,4.947751041,5.490107011,6.030638206\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,3.060846739,3.521460851,4.018442863,4.543620262,5.0875798,5.641208565,6.196580008\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,2.690929891,3.193729678,3.734817295,4.303635525,4.889846122,5.484310415,6.079529102\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,3.306366428,3.813143463,4.348632207,4.903881902,5.469632132,6.037445432,6.600313826\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,14.75853739,15.43056186,15.9850659,16.45031815,16.8481978,17.19534446,17.50422517\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,14.6602735,15.31943425,15.85907654,16.30859385,16.69044348,17.02160384,17.31478006\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,14.43654241,15.15066571,15.73962546,16.23278623,16.65302525,17.01789303,17.34067957\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,15.33463832,15.93409602,16.42339217,16.82973096,17.17385556,17.47149302,17.73447997\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,9.583518815,10.25895621,10.9313062,11.59468009,12.24239225,12.868521,13.46854507\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,9.688054759,10.36319047,11.03057617,11.68631841,12.32515754,12.94212023,13.53327429\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,9.660779403,10.34327132,11.02065994,11.68687983,12.33549396,12.96095073,13.55909275\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,9.65045365,10.30561515,10.95766268,11.60183604,12.2321522,12.84304393,13.4300928\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,9.579580513,10.26262929,10.93791378,11.60117661,12.24697259,12.87024234,13.46702585\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,9.715860509,10.40275592,11.0822153,11.74876628,12.39646012,13.02013371,13.61592986\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,17.27291263,17.73037814,18.10541263,18.41922981,18.68779575,18.92299989,19.13358856\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,15.95658003,16.30692411,16.59171779,16.82900201,17.03208673,17.21075697,17.37213564\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,15.15652184,15.63569621,16.02733354,16.35372379,16.63164184,16.87362983,17.08898205\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,16.89937662,17.36190353,17.73987912,18.05425276,18.32096154,18.55208259,18.75670584\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,12.75660799,13.57983311,14.31760137,14.98215626,15.58291268,16.12740694,16.6219122\n\"linker NCCCCCCN, [C]#N, nodes [Cd], [Ni], topology hms\",,,13.04470341,13.78878454,14.46938702,15.09263181,15.6634918,16.1862793,16.66491625\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,17.39677549,18.09322134,18.66690843,19.1430706,19.54133465,19.8769669,20.16188036\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,17.36420216,18.06418354,18.64104029,19.11998974,19.52068333,19.85842653,20.14517407\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,3.22962043,3.912783704,4.617756528,5.326356526,6.024471658,6.702049322,7.352592752\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,3.579643043,4.231232507,4.899185666,5.568685163,6.228173509,6.86931874,7.486639752\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,3.232566002,3.915786414,4.620760884,5.329320844,6.027365942,6.70485303,7.355292729\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,3.582052321,4.233417594,4.901163593,5.570473082,6.229788606,6.870777858,7.487958991\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.662399595,8.486105742,9.295812913,10.08715873,10.85557548,11.5968837,12.30767015\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.125791628,7.974587603,8.80980925,9.625387737,10.41621614,11.17812543,11.90792238\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.277295828,8.139765452,8.986894403,9.811542277,10.6083812,11.37346295,12.10400326\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,6.848512833,7.628845945,8.40559918,9.17220352,9.923149978,10.65377913,11.36025392\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.664454291,8.487535048,9.296676563,10.08753484,10.8555445,11.59652073,12.30704179\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.123974311,7.973556043,8.80940469,9.625495418,10.41674612,11.17900305,11.90908368\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.291182697,8.151908171,8.997519792,9.820859614,10.6165801,11.38071084,12.1104447\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,6.840109036,7.622394578,8.400819807,9.16886063,9.921033865,10.6526996,11.36003923\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.655303155,8.479393057,9.289410482,10.08101883,10.84966758,11.59118869,12.30217629\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.121872896,7.970788207,8.806042142,9.62161423,10.41242621,11.17432505,11.90412548\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.288378718,8.149342482,8.995171093,9.818692941,10.61455759,11.37879806,12.10861348\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,6.847867612,7.628426913,8.405373993,9.172152744,9.923258838,10.65403369,11.36063972\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.648248819,8.472599324,9.282868907,10.07473295,10.84364378,11.58543182,12.29668801\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.121753115,7.971569793,8.807644984,9.623946177,10.4153882,11.17781661,11.90804948\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,7.280846661,8.144839749,8.992895131,9.818054853,10.61511909,11.38023016,12.11066817\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,6.847373533,7.629472423,8.407745039,9.175621453,9.927604479,10.65905448,11.36615859\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,9.120409236,9.970184332,10.78266644,11.55571279,12.28812616,12.9794731,13.62996687\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,9.332594707,10.13057249,10.89643082,11.62847418,12.3254825,12.98673665,13.61202122\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,9.115414606,9.964789375,10.77704653,11.55000441,12.2824308,12.97386355,13.62449349\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,9.336055509,10.13323777,10.89845231,11.62997615,12.32656585,12.98748305,13.61249679\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.80943998,14.71229789,15.52320241,16.25168166,16.90650139,17.49559905,18.0261057\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.26582081,16.84420978,17.36014536,17.82526925,18.24812749,18.63501004,18.99060806\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.89816935,14.77273303,15.55859175,16.26541404,16.90188736,17.47573425,17.99379375\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.22842058,16.80502454,17.3194966,17.78366038,18.20596629,18.59257479,18.94808282\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.81494824,14.71599807,15.52583245,16.25367517,16.9081119,17.49697428,18.02733139\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.42284758,16.98166775,17.48149255,17.93320757,18.3447912,18.7221028,19.06950382\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.82486074,14.70626422,15.49840171,16.21093942,16.85257717,17.43106359,17.95327355\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.09329333,16.68790859,17.21711532,17.69345465,18.12591932,18.52108169,18.88385402\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.80933262,14.71076639,15.52091538,16.24904959,16.90377067,17.49291284,18.02354293\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.45676661,17.00981894,17.50506739,17.95309142,18.36165961,18.73648282,19.08181408\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.86644401,14.74148848,15.52827725,16.23630431,16.87413508,17.44940808,17.96890566\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.23332307,16.80966287,17.32401438,17.78813428,18.21043194,18.59704282,18.95254919\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.81183866,14.71343177,15.52353675,16.25151836,16.90603571,17.49495706,18.02536857\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.11683215,16.71689442,17.2499486,17.72884057,18.16294911,18.55915409,18.92257333\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,13.84885428,14.72821643,15.51856848,16.22950064,16.86967724,17.44682898,17.96781981\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology lvt,the\",,,16.29380667,16.86092401,17.36773259,17.82562195,18.24273115,18.62499265,18.97683305\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,22.17870944,22.43715486,22.63777997,22.79656691,22.92436431,23.02873174,23.1150615\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,22.0506786,22.32767141,22.54319068,22.71408337,22.85183571,22.96447937,23.05775932\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.547099526,4.226189455,4.927393323,5.631269518,6.323338917,6.993617723,7.635846488\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.600935896,4.275789243,4.972110341,5.670922023,6.358039409,7.023638973,7.661528787\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.588675263,4.267900038,4.968637679,5.671617759,6.362480697,7.03132115,7.67192932\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.567546863,4.24494977,4.944505036,5.646894228,6.337676739,7.006863527,7.648171467\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.113460067,3.589104953,4.099228958,4.635140872,5.187450969,5.747348452,6.307315097\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,2.901604914,3.348557654,3.83329774,4.348229294,4.884388705,5.432916311,5.985947882\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.418488038,3.916543152,4.449753191,5.006362927,5.575363397,6.147337236,6.714803411\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.361255535,3.829638828,4.333219328,4.862630165,5.408156469,5.960879801,6.513300463\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.092751502,3.536194538,4.017048625,4.527261709,5.057809211,5.599956448,6.14603035\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.267085541,3.732207405,4.234079586,4.763163618,5.309529192,5.864036422,6.418977022\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,2.935370865,3.383663396,3.869003091,4.383928221,4.919608088,5.46730179,6.019244792\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.124366949,3.599395955,4.108702628,4.643673105,5.194985668,5.75388218,6.312881059\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.429554997,3.927559296,4.460746222,5.017313954,5.586226232,6.158052212,6.725306542\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.368630585,3.83642992,4.339613433,4.868736516,5.414022227,5.966504092,6.518646772\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.245973392,3.712119981,4.214864766,4.744660198,5.291584232,5.846508863,6.401735643\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.07344843,3.519107576,4.002235354,4.514635871,5.047196688,5.591135828,6.138760779\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.531299842,4.203984969,4.900773373,5.601920716,6.292577929,6.962412787,7.604874813\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.59257299,4.271876474,4.972915653,5.676357163,6.367779469,7.037232732,7.678483144\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.568768046,4.246964684,4.947180626,5.650029536,6.34106584,7.010326162,7.65156373\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.590312076,4.268364728,4.967585065,5.66892352,6.358176218,7.025535683,7.664845449\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.120517822,3.59344201,4.101005714,4.634613012,5.184932916,5.743182504,6.301848025\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,2.969371879,3.420192562,3.90769079,4.424293058,4.961115279,5.509409946,6.061438461\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.43537495,3.933945332,4.467130198,5.023333197,5.591671619,6.162820767,6.729363887\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.367534581,3.836864526,4.34104006,4.870744892,5.416313112,5.968866814,6.520937607\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.068561136,3.511458491,3.991850043,4.501724818,5.032080351,5.574185836,6.120358176\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.248918426,3.714989291,4.217571206,4.747182207,5.293938382,5.848731724,6.403872593\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,2.918251525,3.365934216,3.850984084,4.365881719,4.90174386,5.449783909,6.002198857\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.116851291,3.592301991,4.102230248,4.637948076,5.190068657,5.74978308,6.309574044\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.41326707,3.91068715,4.443441259,4.999755085,5.568595098,6.140518733,6.708021635\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.370531481,3.838883001,4.342378539,4.871646201,5.416974114,5.96945084,6.52158505\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.252939129,3.719532004,4.222750121,4.753026444,5.300415712,5.855772193,6.411387769\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.080852996,3.526717313,4.009897557,4.522242872,5.054670869,5.59841988,6.145811468\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.556381203,4.23509993,4.935965033,5.639543734,6.331349808,7.001387686,7.643386874\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.573707373,4.253382912,4.954702139,5.658360217,6.349966789,7.019589645,7.66099674\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.503162663,4.174466424,4.870529717,5.571519137,6.262472523,6.932946499,7.576293071\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.532177854,4.205216831,4.902250146,5.603576715,6.294372035,6.964316514,7.606865594\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.124976435,3.59973361,4.108990238,4.644080043,5.195631528,5.754846095,6.314212617\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,2.947708549,3.397118362,3.883686727,4.399808674,4.936546063,5.48508965,6.037640322\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.418089721,3.915370599,4.4478053,5.003694321,5.572056727,6.143483052,6.710487295\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.36070301,3.828882682,4.332335842,4.861667418,5.407132939,5.959785689,6.512101136\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.069231471,3.513478498,3.995335301,4.506652429,5.038338335,5.581613,6.128773307\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.256546273,3.724533581,4.229079142,4.760529736,5.308891354,5.864997287,6.421137545\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,2.959605463,3.409981914,3.897182967,4.413631078,4.950428711,5.49881005,6.051016592\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.118944186,3.59232608,4.100319323,4.634312413,5.184966325,5.743496137,6.302390218\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.435630427,3.934925197,4.468689987,5.025348032,5.594034029,6.165439406,6.73216229\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.368767816,3.838531399,4.343041214,4.872998485,5.418750317,5.971429602,6.52357739\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.255896072,3.720742524,4.222179041,4.750772023,5.296656107,5.850724438,6.405279069\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,3.074976499,3.517492534,3.997583042,4.50721507,5.037362668,5.5792755,6.125256212\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.350567539,9.981085728,10.62983701,11.28528739,11.93705238,12.57651833,13.19701992\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.311855537,9.939471761,10.58638567,11.24104074,11.8929168,12.5332173,13.15508942\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.302823562,9.935542397,10.58683583,11.24521783,11.90022645,12.54311926,13.16709712\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.301086762,9.93158117,10.5802437,11.23567991,11.88757138,12.52733221,13.14830267\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.470978994,10.32607113,11.15251439,11.94261686,12.69135741,13.39598727,14.05556895\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.63555308,11.29791028,11.95812802,12.60838444,13.24127113,13.85080693,14.432733\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.82338025,10.58867108,11.34547408,12.0820347,12.78982276,13.46323623,14.09908874\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.431655958,10.28772682,11.11564583,11.90751664,12.65817234,13.36476436,14.02628921\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.63583148,11.29751438,11.9573113,12.60730974,13.24004018,13.84948143,14.43134879\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.841890605,10.60666489,11.36248113,12.09776397,12.80412037,13.47604739,14.11042609\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.313998818,9.935636173,10.57606265,11.22426963,11.87014557,12.50514747,13.12254513\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.326657749,9.954620934,10.60119684,11.25516339,11.90621956,12.54569748,13.16681054\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.336023298,9.965155447,10.61288703,11.26778867,11.9194725,12.55926072,13.1803992\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.278387219,9.911881754,10.56347633,11.22166721,11.87607252,12.5180778,13.14101875\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.458354079,10.31315407,11.14021592,11.93147348,12.68164503,13.38780844,14.04891618\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.63496883,11.30163412,11.96584229,12.61953921,13.25523408,13.86695285,14.45049099\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.81423107,10.58096699,11.33884911,12.07625624,12.78473292,13.45871898,14.09505207\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.454128577,10.30890217,11.13555886,11.92620557,12.67568398,13.38115358,14.04161658\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.63773131,11.29889724,11.95825646,12.60789301,13.2403315,13.84954367,14.43123739\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.821719595,10.58692032,11.34330102,12.0792546,12.78635601,13.4590739,14.09426584\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.296353334,9.929826703,10.58213334,11.2415689,11.89754322,12.54125435,13.16588847\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.27105726,9.906912184,10.56236999,11.22531135,11.88482678,12.53189874,13.1595855\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.292687008,9.916318661,10.55849708,11.20827411,11.85556456,12.49183896,13.11037692\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.318565006,9.942940311,10.58639409,11.23772749,11.88663424,12.52442121,13.14426321\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.460406219,10.31396684,11.1396154,11.92945417,12.67830375,13.3832962,14.04340572\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.62671905,11.28858432,11.94846665,12.59853811,13.23136909,13.84095255,14.42300409\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.838526887,10.60529303,11.3631277,12.10031483,12.80837855,13.48177628,14.11737926\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.461174748,10.31628675,11.14347138,11.93471863,12.68479079,13.39079863,14.05171837\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.63015404,11.29778414,11.96261048,12.61671666,13.25269655,13.86462706,14.44833373\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.789897832,10.55674265,11.31484678,12.05263034,12.76163492,13.4362769,14.07336347\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.29773109,12.01962222,12.73510818,13.43420384,14.1090382,14.75396817,15.36537333\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.537406962,10.22726595,10.92128821,11.61324972,12.29599405,12.96273196,13.60775644\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.3435831,12.13720485,12.91714652,13.67256252,14.39505707,15.0789567,15.72104727\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.64863204,11.43078759,12.20687311,12.96527023,13.6966085,14.39414647,15.05361087\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.47386738,12.21761352,12.94907893,13.65890789,14.34001216,14.98755201,15.59865614\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.654704474,10.34651219,11.03933768,11.727925,12.40591368,13.06711314,13.70624203\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.40654256,12.2099619,12.99701905,13.75699836,14.48186391,15.16637402,15.80773191\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.75549206,11.51523423,12.27157427,13.01301529,13.73007143,14.41576163,15.06552093\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.47388652,12.21789025,12.94969008,13.65982597,14.34116618,14.98886232,15.60005115\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.736743095,10.42721898,11.12073775,11.81105748,12.49107384,13.15411081,13.79461347\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.39060618,12.20160352,12.9950796,13.76032853,14.48940917,15.17721077,15.8210758\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.73674295,11.51375509,12.28483843,13.03839035,13.76506665,14.45815382,15.11340175\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.17117862,11.88918951,12.60206508,13.30001142,13.97509391,14.62148249,15.23532669\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.305031233,9.995960693,10.68987367,11.38127256,12.06365874,12.73070062,13.37694097\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.25940571,12.02809354,12.78936756,13.53157502,14.2454203,14.92435405,15.56437379\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.63836839,11.40895779,12.17536328,12.92596403,13.65125529,14.34429636,15.00059181\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.55059313,12.29948397,13.03445917,13.74627959,14.42806338,15.07520777,15.68507332\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.890095119,10.57832493,11.26823054,11.95405028,12.62900608,13.28664952,13.92158959\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.53498824,12.35624675,13.15647184,13.92538087,14.65553463,15.3423329,15.98359209\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.80187786,11.54977897,12.29552228,13.02762213,13.73660143,14.41544492,15.05951025\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.43835045,12.19822056,12.94380138,13.66578372,14.35714564,15.01316066,15.6311122\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.724093532,10.42046726,11.11661378,11.80737636,12.48651871,13.14799063,13.78665611\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.46528739,12.26765217,13.05426601,13.81397834,14.53849932,15.22246047,15.86302062\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.8618139,11.59979497,12.33741429,13.06286512,13.76639372,14.44075639,15.08112551\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.50115756,12.24077474,12.96878245,13.67568301,14.35429049,14.99969451,15.60896952\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.7814217,10.4691955,11.15929775,11.84595838,12.52236155,13.18199266,13.81937566\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.45828298,12.27300622,13.06788794,13.83288879,14.56057877,15.24623151,15.88747293\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.72356457,11.49503432,12.26132908,13.01099645,13.73469878,14.42564899,15.07948667\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.22091481,11.94286082,12.65844012,13.35801805,14.03383008,14.68021298,15.29347013\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.40773753,10.0993886,10.79280837,11.48285394,12.16326385,12.82787311,13.47134928\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.28480723,12.06358385,12.83244483,13.58013721,14.29773341,14.97901499,15.62026877\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.62444857,11.40119089,12.17301243,12.92829448,13.65754565,14.3538605,15.01279852\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.36506025,12.09719889,12.82046679,13.52503012,14.20330473,14.84998254,15.46177391\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.558560829,10.2541386,10.95306495,11.6490368,12.33489846,13.00391811,13.65047932\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.34376509,12.14517485,12.93196671,13.69302343,14.41992127,15.10708729,15.7514632\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.72223765,11.51057534,12.29147608,13.05321268,13.78648317,14.48471304,15.14383616\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.34362234,12.08728838,12.82022501,13.53267552,14.21722618,14.86877965,15.48426304\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.487446417,10.17547054,10.86818398,11.55915065,12.24118345,12.90751133,13.55244184\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.28103567,12.07352485,12.85338681,13.60929037,14.3326125,15.01757711,15.66092015\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.69881951,11.46226417,12.22359409,12.9705127,13.69302492,14.38385523,15.03829014\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.50458778,12.25327677,12.9886742,13.70138756,14.38440212,15.03300715,15.6444785\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.805458867,10.4943563,11.18585045,11.87386351,12.55140538,13.21188064,13.84979279\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.53388407,12.34901661,13.14498623,13.91101826,14.63930921,15.32498813,15.96566963\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.80579365,11.55582057,12.30346122,13.03715692,13.74741037,14.42721907,15.07197139\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.45717339,12.21497838,12.95838493,13.67820753,14.36750829,15.02161423,15.6378383\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,9.780618291,10.47672995,11.17245754,11.86257824,12.54083316,13.20118218,13.83851949\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,11.4616724,12.27218051,13.06554129,13.83069314,14.55946733,15.24664053,15.88952554\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Fe], topology pcu,\",,,10.89720498,11.63588824,12.37381955,13.09921098,13.80235116,14.47605164,15.11554354\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.18879869,20.62297952,20.96654017,21.24253025,21.4672535,21.65246067,21.80676927\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.27147865,20.69148068,21.02420106,21.29173001,21.50972977,21.68950958,21.8393756\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.19133375,20.62509857,20.96833572,21.24406988,21.46858754,21.65362724,21.80779774\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.25794742,20.67999185,21.01434195,21.28318776,21.50226423,21.68293404,21.83354319\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.28871827,20.70537557,21.03569397,21.30143673,21.51806611,21.69676585,21.84576112\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,11.21598793,12.19536947,13.10778153,13.95246769,14.7302082,15.44317975,16.09462611\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,11.21538384,12.19451519,13.10677509,13.95137733,14.72908088,15.44204733,16.09350972\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.409777625,4.060614709,4.734319728,5.414033319,6.086369616,6.741568996,7.373136569\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.09789804,3.747216617,4.423923646,5.110102976,5.791398183,6.457227591,7.100438087\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.209432475,3.866945882,4.551119281,5.243567608,5.929727625,6.599014709,7.244405103\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,4.704069562,5.652807287,6.563451414,7.418586492,8.209651853,8.934101907,9.593175947\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.40974137,4.060604836,4.734332536,5.41406453,6.086415069,6.741624976,7.373199936\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.098583159,3.747892354,4.424583296,5.110741181,5.792011131,6.457812893,7.100994537\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.208561919,3.866053751,4.55022048,5.242674206,5.928848868,6.598157347,7.243573817\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,4.706615163,5.655436464,6.566091295,7.421184297,8.212171899,8.936521819,9.595483138\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,9.32847752,10.1196744,10.88622559,11.62433135,12.33074485,13.00312613,13.6400991\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,7.827679788,8.70337357,9.552839244,10.37296838,11.16096634,11.91448014,12.63175409\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,9.120525835,9.924137329,10.69921785,11.44344044,12.15461057,12.83109249,13.47195013\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,7.728476431,8.519169929,9.295894378,10.05612373,10.79655969,11.51374776,12.20455619\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,7.580028008,8.37679362,9.158698683,9.923241887,10.66730413,11.38765089,12.08134903\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.45853878,7.254489705,8.048255883,8.833512109,9.604506405,10.35612866,11.08405041\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,9.229302996,10.02222108,10.79034181,11.52982761,12.23749938,12.91111334,13.54937984\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.591118073,7.387671255,8.17713085,8.953753721,9.712913002,10.45070784,11.16387588\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,9.328146977,10.1193458,10.88590899,11.62403117,12.33046248,13.00286144,13.63985122\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,7.826472793,8.702251675,9.551807533,10.37202664,11.16011086,11.91370517,12.63105292\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,9.119857875,9.923431413,10.69849753,11.44272148,12.15390329,12.83040341,13.47128323\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,7.728251336,8.518974322,9.295730006,10.05598943,10.79645264,11.51366443,12.2044929\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,7.579427042,8.376245207,9.158184146,9.922751105,10.66683173,11.38719413,12.08090656\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.457331404,7.253343703,8.047125896,8.832373789,9.603349303,10.35495106,11.08285571\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,9.22860705,10.02158246,10.78975298,11.52928292,12.23699426,12.91064394,13.5489428\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.590691632,7.387311204,8.176848392,8.953549322,9.712781602,10.45064182,11.16386672\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,16.13697095,17.16904795,18.0241738,18.73733903,19.33628774,19.84286103,20.27424924\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.64136111,15.58429737,16.41946396,17.15998982,17.81719245,18.40102192,18.92029314\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.49918422,15.3452799,16.10149789,16.77942482,17.38867144,17.93734331,18.43237472\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.79396537,15.60127576,16.3114642,16.94162995,17.50478769,18.01099445,18.46815563\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.65710571,15.44471831,16.15378615,16.79334452,17.37134982,17.89472644,18.36948387\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.60523929,15.38689873,16.08339464,16.70758454,17.26981493,17.77842691,18.24019471\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.45219087,15.3623118,16.17560642,16.90289061,17.55354126,18.13589502,18.65745051\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,13.74438364,14.73684426,15.61938062,16.40521879,17.10576708,17.7309854,18.28964655\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,16.14164336,17.17324514,18.02794393,18.74073047,19.33934559,19.8456258,20.27675661\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.63020112,15.57453525,16.41090543,17.1524591,17.81053708,18.39511249,18.91502099\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.46753068,15.31694568,16.07600324,16.75637573,17.36774238,17.91826352,18.41491738\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.771013,15.58116064,16.2937787,16.92602448,17.49096507,17.99870316,18.4571831\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.64343256,15.43230596,16.14250243,16.78306744,17.36196921,17.88614411,18.36161304\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.64625437,15.42308912,16.11550549,16.7362295,17.29549932,17.80156798,18.26113838\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.44936317,15.35977425,16.1732992,16.90077311,17.55158532,18.13408033,18.65576168\n\"linker [O-]C(=O)c1cc(cc(c1)P(=O)([O])[O])C(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,13.80574839,14.79148567,15.66815761,16.44890266,17.14503051,17.76640669,18.32171961\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,21.85243883,22.20499781,22.48263761,22.70485899,22.88529386,23.03367712,23.15709577\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,21.89091569,22.23644584,22.5087926,22.72693863,22.90417432,23.05000315,23.17135141\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,21.85438509,22.20664648,22.48404909,22.70607922,22.88635811,23.03461275,23.15792429\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,21.88852798,22.23439395,22.50701641,22.72538971,22.90281394,23.04880034,23.17028129\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.250186553,3.864906014,4.503790416,5.152435519,5.798766223,6.433467435,7.049911949\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.127991585,3.765631086,4.433081087,5.11234923,5.788777967,6.451418844,7.092764406\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.167255525,3.79734949,4.457189908,5.129300065,5.799306254,6.45638024,7.093029309\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.086750594,3.704281225,4.348265637,5.003391209,5.656937527,6.299149115,6.923108361\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.192878432,3.875780256,4.578895921,5.284887831,5.980250929,6.655321051,7.303818129\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.26225299,3.942513288,4.641165468,5.34161135,6.030934746,6.699889192,7.342462533\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,2.949184083,3.584566686,4.246308355,4.918226261,5.587171443,6.243267727,6.879668216\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.254411135,3.949622642,4.661846695,5.374077671,6.073261844,6.750204728,7.399060427\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.266337132,3.879838873,4.517383826,5.164673444,5.809698675,6.443181251,7.058510817\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.125486164,3.764532762,4.433271364,5.113642441,5.790953267,6.454240473,7.095994079\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.164075377,3.793370466,4.452470231,5.123949003,5.793453126,6.450154875,7.086551137\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.075166717,3.693679432,4.338696419,4.994830201,5.649317853,6.292383115,6.917101302\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.18517904,3.86638385,4.568336033,5.273609368,5.968605634,6.643576185,7.292170156\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.272752954,3.954352801,4.653949875,5.35499004,6.044615518,6.713639206,7.356102643\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,2.934163202,3.567279894,4.227313897,4.898065943,5.566344807,6.222223379,6.858803901\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.261634112,3.957677794,4.670418049,5.38289755,6.082120691,6.758947805,7.407579227\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.249668837,3.864340491,4.503189815,5.151812229,5.798131284,6.432830118,7.049279702\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.127916942,3.765581629,4.4330539,5.112340977,5.788785327,6.451438724,7.092794034\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.167004384,3.797014198,4.456782645,5.128834866,5.798797145,6.455840124,7.092469418\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.086613679,3.704180615,4.348202276,5.00336339,5.656941993,6.299181855,6.923165152\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.1924141,3.875299056,4.578402796,5.284388186,5.979749995,6.654823524,7.30332801\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.26204259,3.942337193,4.641018148,5.341487779,6.030830532,6.699800591,7.342386393\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,2.949294969,3.584701383,4.246460065,4.918389228,5.587341021,6.243440294,6.87984103\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.254328483,3.949547209,4.66177609,5.374010183,6.073196362,6.750140604,7.398997339\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.266801001,3.880307325,4.517854055,5.165142454,5.810163526,6.443639264,7.058959699\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.125615376,3.764613741,4.433313016,5.113652931,5.790939668,6.454208699,7.095948966\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.164329841,3.793592484,4.452665218,5.124121436,5.793606629,6.450292362,7.086674946\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.075314839,3.69378446,4.338761995,4.994861159,5.649319379,6.292360248,6.917058663\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.184917671,3.866058017,4.567960658,5.273198251,5.968170785,6.643127654,7.291716128\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.272866614,3.954440286,4.654016476,5.355040245,6.044652919,6.713666566,7.35612202\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,2.934357002,3.56750429,4.227566789,4.898343544,5.566642536,6.222536479,6.859127836\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,3.261862627,3.957880284,4.670598765,5.383060085,6.082267963,6.759082129,7.407702422\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.150140455,9.910274339,10.65238791,11.3725626,12.06721467,12.73341831,13.36904917\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.518628388,10.28331482,11.02026401,11.72878711,12.40765594,13.05566285,13.67192337\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.767746335,8.549817954,9.317743197,10.06958198,10.80250794,11.51338143,12.19923643\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.484072853,10.24500835,10.97878384,11.68470162,12.36151716,13.0079945,13.62320944\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.19086961,9.963724709,10.71604722,11.44419594,12.144865,12.81539738,13.45392243\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.863846716,7.739817078,8.591393671,9.413662915,10.20377345,10.96007722,11.68167645\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.565006571,8.370035546,9.155948184,9.921674154,10.66526991,11.38439749,12.07676065\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.911368598,7.780685485,8.632981996,9.462791331,10.26579493,11.03858043,11.77857185\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.589830308,8.390588174,9.172791245,9.935519595,10.67682835,11.39429815,12.08551954\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.821390397,7.696807133,8.549374886,9.373609169,10.1662504,10.92536619,11.6498656\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.155114189,10.01737182,10.82968378,11.59510683,12.31626942,12.99536548,13.63428861\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.195124719,10.05552473,10.86804327,11.63482717,12.35788267,13.03900173,13.67983274\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.587936515,8.418835579,9.233617835,10.0290538,10.8014032,11.5470336,12.26284488\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.03027146,7.937457429,8.824467217,9.685172659,10.51480181,11.30974848,12.06748258\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.103823786,7.966995553,8.817015253,9.647534673,10.45314946,11.22945661,11.97310401\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.417783686,10.2630306,11.05859514,11.80829382,12.51503195,13.18103688,13.80812493\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.041582708,9.915181259,10.73874316,11.51492611,12.24610793,12.93435066,13.58150188\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.731904411,7.528476487,8.322028652,9.105955489,9.874594028,10.623066,11.34729785\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.714904668,7.527514472,8.331086466,9.120741298,9.892092064,10.64120707,11.36471225\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.194798109,9.952438083,10.69166454,11.40881032,12.10045949,12.76378965,13.39673402\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.553401149,10.31813022,11.05454053,11.76215091,12.43988098,13.08662332,13.70155929\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.778990587,8.561743433,9.330183371,10.08237425,10.81550257,11.52644606,12.21225799\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.500189779,10.26176596,10.99544054,11.70077207,12.37671004,13.02215655,13.63628118\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.217790441,9.992602778,10.74590419,11.47433649,12.17480564,12.84480809,13.48258305\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.888930819,7.761048193,8.609695646,9.429712735,10.21806534,10.97297225,11.69343962\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.537800481,8.342775899,9.128929247,9.895109444,10.63931431,11.35916164,12.05232084\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.89627645,7.765701674,8.61828377,9.448492801,10.25196702,11.02526448,11.76578882\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.593229856,8.392639733,9.173747709,9.935630613,10.6763177,11.39335377,12.08429178\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.802543769,7.681368986,8.537150819,9.364347117,10.15966528,10.9211597,11.64774123\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.19833571,10.05638539,10.86496304,11.62709951,12.34537613,13.02193555,13.65862323\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.180715509,10.04178076,10.85509785,11.62272984,12.3466308,13.02856233,13.67015677\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.580488577,8.411196818,9.225902314,10.02136107,10.79381495,11.53961321,12.25563887\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.012865979,7.918959068,8.805218329,9.66546102,10.49487,11.28979859,12.04767981\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.1252198,7.984860769,8.832020092,9.660178043,10.4638176,11.23845865,11.98069353\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.425481561,10.26909866,11.06329486,11.8118451,12.51762379,13.18283359,13.80927008\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.044030089,9.918429459,10.74275595,11.51960188,12.25132159,12.93997634,13.58742409\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.734882004,7.532876997,8.327657632,9.112642446,9.882175439,10.63138263,11.35619748\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.713081293,7.52699964,8.331615059,9.122035785,9.893902383,10.64332679,11.36698116\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.149391749,9.909520644,10.65162359,11.37178785,12.0664328,12.73263397,13.36826732\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.518564362,10.28325944,11.02021295,11.72873769,12.40760666,13.055613,13.67187272\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.767513176,8.549581174,9.3175011,10.06933451,10.80225619,11.51312712,12.19898148\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.484592499,10.24545833,10.97917201,11.6850359,12.36180502,13.00824269,13.62342388\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.190700606,9.963569017,10.71589705,11.44404802,12.14471858,12.81525289,13.45378076\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.863925451,7.739887699,8.591448952,9.413698759,10.20378821,10.96007101,11.6816505\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.564969517,8.370004491,9.155921394,9.921650313,10.66524804,11.38437691,12.07674088\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.910984787,7.780313481,8.63261737,9.462431543,10.26543893,11.03822818,11.77822392\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.589464039,8.390271755,9.172517503,9.935281893,10.67662081,11.39411576,12.08535806\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.821588313,7.696945077,8.549465352,9.373662122,10.16627393,10.92536688,11.64984881\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.154039747,10.01640707,10.82880946,11.59430759,12.31553323,12.99468291,13.63365234\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.194205925,10.05474159,10.86736346,11.63422597,12.35734158,13.03850712,13.67937471\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.58755731,8.418487193,9.233294799,10.02875204,10.80111973,11.54676623,12.26259198\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.029981264,7.937187475,8.824212344,9.684929334,10.51456775,11.30952229,12.06726347\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.103292946,7.966515079,8.816575937,9.647129665,10.45277361,11.22910596,11.97277552\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.417044807,10.26237601,11.05801571,11.80778109,12.51457824,13.18063521,13.80776908\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.041212767,9.914876522,10.73848717,11.51470597,12.24591392,12.93417563,13.58134068\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.731103596,7.527772388,8.321400503,9.105387422,9.874074086,10.62258525,11.34684966\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.714206308,7.52697277,8.330666786,9.120415746,9.89183853,10.64100827,11.36455482\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.195492202,9.953056615,10.69222224,11.40931903,12.1009284,12.76422575,13.39714253\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.554419643,10.31900784,11.05530161,11.76281578,12.44046623,13.08714232,13.7020228\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.779696291,8.562345075,9.33069334,10.08280463,10.81586451,11.52674952,12.21251171\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.501501113,10.26291156,10.99644329,11.70165198,12.37748437,13.02284005,13.63688642\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.218286392,9.992996975,10.74621015,11.47456703,12.17497241,12.84492149,13.48265213\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.888517393,7.760749641,8.609497949,9.429601607,10.218027,10.97299395,11.69350997\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.538697701,8.343609366,9.129697886,9.895815159,10.63996068,11.35975307,12.05286202\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.896483012,7.765845953,8.61836843,9.448523118,10.25194951,11.02520603,11.76569613\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.593246764,8.392631201,9.17371598,9.935577993,10.67624658,11.39326656,12.0841909\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.802962514,7.6817641,8.53751741,9.364684038,10.15997339,10.92144085,11.64799766\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.199029735,10.05697035,10.86545621,11.62751587,12.34572834,13.02223415,13.65887697\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.181623494,10.04258553,10.85581351,11.62336928,12.34720515,13.02908097,13.67062749\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.581202072,8.411852588,9.226503415,10.02191222,10.79432129,11.54007971,12.25607003\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.013048815,7.919050297,8.805229915,9.665405141,10.49475828,11.28964165,12.04748707\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,7.12595302,7.98547237,8.832536041,9.660617256,10.46419428,11.23878372,11.98097562\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.426262754,10.26978065,11.06389658,11.81238189,12.51810778,13.18327425,13.80967474\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,9.045530144,9.919775596,10.74396433,11.52068791,12.25229936,12.94085846,13.58822176\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.737075373,7.534774301,8.329312266,9.114097896,9.883466678,10.63253761,11.35723849\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,6.714561157,7.52828705,8.332732821,9.123005684,9.894744494,10.64405912,11.36761955\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,11.16305777,11.89107598,12.59957278,13.2849954,13.94378121,14.57298332,15.17052406\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,8.607755981,9.498619147,10.3698201,11.21415217,12.0254501,12.79901257,13.5317094\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,11.14007753,11.87167915,12.58295901,13.27056619,13.93108944,14.56169367,15.16038316\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,8.613376602,9.505318158,10.37759277,11.22291664,12.03507613,12.80934592,13.54259015\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,11.1604224,11.88876395,12.59752586,13.28316883,13.94214006,14.57149997,15.16917633\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,8.608240086,9.499001931,10.37011749,11.21437782,12.02561585,12.79912864,13.53178457\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,11.14124666,11.87263973,12.58374992,13.27121919,13.93163026,14.56214309,15.1607579\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,8.613867725,9.505759316,10.37798511,11.22326354,12.03538193,12.8096152,13.54282736\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,15.0054921,15.82739836,16.55423253,17.2010553,17.77976015,18.29982307,18.76890023\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.45727112,15.32558538,16.09149562,16.77177995,17.37961412,17.92542233,18.41755629\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.84302728,14.77333922,15.59434823,16.32329197,16.97398338,17.55751908,18.08289244\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.38602734,14.37656087,15.24954454,16.02301265,16.71173596,17.32774356,17.88086804\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.19063219,15.07745727,15.84581601,16.51775494,17.11088305,17.63903095,18.11298356\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.52533534,15.37478628,16.11115412,16.75576173,17.32549983,17.83355329,18.29015402\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,15.08492637,15.89026225,16.6030095,17.23816392,17.80736359,18.31976982,18.78272819\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.3592683,15.24466407,16.0244171,16.71593917,17.33292718,17.88622203,18.38450529\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.85373806,14.77522538,15.59017638,16.31500466,16.96294935,17.54470739,18.06899183\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.34493158,14.33809222,15.21341801,15.98899273,16.67963017,17.29739389,17.85214274\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.77247602,15.59661319,16.31011212,16.93432217,17.48598752,17.97807891,18.42059795\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.12234314,15.01666737,15.79198051,16.47028433,17.06918587,17.60253427,18.08114378\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,15.01385009,15.83489314,16.56095726,17.20709965,17.78520616,18.30474372,18.77335954\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.4495855,15.31868544,16.08528612,16.76617475,17.37453766,17.92080924,18.41335039\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.83750627,14.76841003,15.58992534,16.31930374,16.97037034,17.55423185,18.07988986\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.38047756,14.37159594,15.24508251,16.01898351,16.7080809,17.32441349,17.87782194\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.18752724,15.07477119,15.84347846,16.51570788,17.10907907,17.63743148,18.11155716\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.53221309,15.38091327,16.11663162,16.76067824,17.32993116,17.8375638,18.29379816\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,15.05661622,15.8653065,16.58092369,17.218532,17.78983375,18.30404658,18.76856389\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.39503242,15.27649564,16.05283625,16.7414081,17.35584466,17.9069275,18.40328616\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.85853733,14.77946548,15.59395926,16.31840761,16.9660318,17.54751576,18.07156307\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,13.3440086,14.33713439,15.21247174,15.98808386,16.67877174,17.29659119,17.85139652\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.76824326,15.59275133,16.30656401,16.93104423,17.48294568,17.97524596,18.41795171\n\"linker [O-]C(=O)c1ccc2c3c1c(ccc3C(=O)N(C2=O)c1ccncc1)C(=O)[O-], nodes [Mn], topology sql\",,,14.11680513,15.01166077,15.78745333,16.46618413,17.06546356,17.59914565,18.07804982\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,17.97787385,18.40715921,18.75351091,19.03622842,19.26951515,19.46394421,19.62748051\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,17.94016534,18.40426257,18.77150626,19.0664771,19.3066069,19.50447381,19.66930521\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,3.380034532,4.05205719,4.742022824,5.433557872,6.114002883,6.774341088,7.408736459\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,3.494576535,4.175249461,4.870461067,5.564359013,6.244856714,6.90346829,7.534808718\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.063404303,6.860839588,7.653873381,8.435882262,9.201451791,9.946062977,10.6660116\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.986856212,7.8010803,8.604062179,9.390788517,10.15648444,10.89691566,11.60862112\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.81850115,7.654349359,8.478293986,9.284430229,10.06754558,10.82327175,11.54819876\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,8.864065851,9.684861157,10.46976245,11.21744988,11.92716767,12.59866681,13.23216616\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.061308316,6.867421426,7.666854965,8.453277575,9.221678513,9.96793887,10.68869552\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.081003366,6.877953453,7.669283526,8.448763843,9.211321442,9.952711636,10.6694358\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.985906888,7.805165576,8.612988319,9.404210345,10.17394168,10.91787965,11.6325382\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.80023965,7.632506103,8.45310698,9.256380308,10.03721383,10.79124921,11.51503485\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,8.869387981,9.6932859,10.48078281,11.2305277,11.94179997,12.61441381,13.24865793\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,6.017622198,6.824792903,7.625057217,8.412242846,9.181433753,9.928558491,10.65026998\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,14.80567841,15.49310108,16.10288899,16.64890723,17.14157051,17.58880965,17.99675959\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,13.41284819,14.25509912,15.02035193,15.71541538,16.34647858,16.91928619,17.43919775\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,14.39313988,15.13040137,15.79166428,16.3882711,16.92891249,17.42043291,17.86837997\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,14.36769331,15.10268278,15.75790715,16.34621923,16.87756422,17.35972358,17.79888005\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,14.54441544,15.26296294,15.89806802,16.4648301,16.97466291,17.43628256,17.85643088\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,13.42320378,14.25687214,15.01622021,15.70724011,16.33556988,16.90657568,17.42535275\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,14.00176156,14.7840681,15.48411179,16.11424484,16.68396787,17.20078661,17.67079744\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni], topology pcu\",,,14.16911136,14.92104562,15.59204797,16.19469584,16.73890526,17.23254346,17.68192477\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,19.55765524,19.70454821,19.81809735,19.90764809,19.9794998,20.03801834,20.08630437\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,19.55388563,19.70140432,19.8154373,19.90536934,19.97752658,20.03629352,20.08478413\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.93358376,6.627220351,7.288078737,7.916013613,8.510691527,9.072068897,9.600649553\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,2.906770598,3.392294893,3.914083117,4.462638598,5.027963647,5.600824132,6.173433074\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.93762892,6.630904305,7.291431314,7.91906663,8.513476143,9.074614177,9.602981821\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,2.906336568,3.392134656,3.914115485,4.46280213,5.028212583,5.601124587,6.173759888\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.652625319,6.377515192,7.069063595,7.725607075,8.346105398,8.930298504,9.47875312\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,3.104478832,3.61448508,4.158115725,4.725443368,5.306479698,5.892332566,6.475747003\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.654472032,6.379342327,7.070844653,7.727326111,8.347753593,8.931871738,9.480250324\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,3.104544944,3.614090279,4.157337139,4.724349015,5.305130143,5.890781447,6.474041209\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.933686219,6.627317112,7.288175678,7.916114798,8.510799526,9.072185112,9.600774525\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,2.906922968,3.392445057,3.914230367,4.46278301,5.028105774,5.600964763,6.173573084\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.934346582,6.627940963,7.288778248,7.916704153,8.511379518,9.072757135,9.601338581\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,2.905877009,3.391693244,3.913690152,4.4623948,5.027826393,5.600762421,6.173423765\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.654389982,6.379180562,7.070601502,7.727008899,8.347373771,8.93144196,9.479782796\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,3.105233615,3.615145203,4.158699709,4.725964321,5.306947029,5.892753189,6.476126138\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,5.650959472,6.37616944,7.067974062,7.72472071,8.345379797,8.929700506,9.478257093\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,3.104805059,3.614331599,4.157574053,4.724589495,5.305377611,5.891036376,6.474302324\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.901489131,10.63387903,11.34510947,12.03372981,12.69708901,13.33247839,13.93772484\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.877233381,10.61228173,11.32589017,12.01660596,12.68179614,13.31877886,13.92541013\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.978689951,10.69577632,11.39341938,12.07014229,12.72324102,13.3499095,13.94784163\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.957686785,10.67777542,11.37786121,12.05658925,12.71134832,13.33940314,13.93850203\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.898548805,10.63091522,11.34217895,12.03087293,12.69433352,13.32984212,13.93521785\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.860892645,10.5968423,11.31128889,12.00278992,12.66872033,13.30640339,13.91369811\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.977214005,10.69463985,11.39254024,12.06945913,12.72270762,13.34949082,13.94751103\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.960404438,10.68001487,11.37970813,12.05811459,12.71261081,13.34045115,13.93937513\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.580947164,10.39487937,11.18699306,11.94907028,12.67512176,13.36139858,14.00608651\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.555535464,10.36960533,11.1620542,11.92466282,12.65141021,13.33850576,13.9840943\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.551168048,10.36565266,11.15846491,11.92139377,12.64842489,13.33577274,13.98158624\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.576778241,10.39080324,11.18303741,11.94525435,12.67145772,13.35789297,14.00274156\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.41326631,11.16336451,11.89955453,12.6163295,13.30817728,13.97052069,14.60007114\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.42932451,11.17764416,11.91237899,12.62793539,13.31874223,13.98018224,14.60893911\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.5436797,11.27375302,11.99295208,12.69531959,13.37496644,14.02699073,14.64782214\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.49571311,11.22873805,11.95050309,12.65519144,13.33699362,13.9910499,14.61381052\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.44018308,11.18761239,11.92148871,12.63625369,13.32634816,13.98715449,14.61535027\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.43358447,11.18144833,11.91579572,12.63102029,13.3215403,13.98273018,14.61126726\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.54219239,11.2726127,11.99208309,12.69466,13.37446652,14.02661136,14.64753309\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,10.52603354,11.25744995,11.97771497,12.68098385,13.36143169,14.0141918,14.63571224\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.633286365,10.37300823,11.09777495,11.80579942,12.49361178,13.15739059,13.7937606\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.628850233,10.36976582,11.09551026,11.80431946,12.49275162,13.15701346,13.79375539\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.650856202,10.39041604,11.11492528,11.82260422,12.50999472,13.17328984,13.80912973\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,9.636230491,10.37567224,11.10013815,11.8078651,12.49539717,13.15892015,13.79506165\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,21.91978512,22.18261729,22.38674475,22.54820856,22.67799005,22.78378876,22.87112079\n\"linker n1ncn(c1)CCn1cnnc1, nodes Cl[Cd], topology \",,,21.91865737,22.18167304,22.38594321,22.54752005,22.67739248,22.78326539,22.87065872\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,20.1428684,20.49439527,20.7737416,20.99903931,21.18315737,21.33540601,21.4626396\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,20.17989154,20.52573787,20.80058221,21.02225923,21.20342687,21.35324272,21.4784489\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,20.78345471,21.05498501,21.26647253,21.43426217,21.56954224,21.68016119,21.77174702\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.202613964,3.85879733,4.5406031,5.230037629,5.912860367,6.578702067,7.220655649\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.413462302,4.067414101,4.745073611,5.428897378,6.105058663,6.763542084,7.397727975\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.334354758,3.987686423,4.665364612,5.349833876,6.027235143,6.687509753,7.323990358\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.352364785,4.007653937,4.686608311,5.371792764,6.049443993,6.709576047,7.345575772\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.685971974,4.39513174,5.122364332,5.847376475,6.555480092,7.236933177,7.885980249\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.725797796,4.432263424,5.155932591,5.876960652,6.581001103,7.258543273,7.903971259\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.207724964,3.863902885,4.54563123,5.234935975,5.917593319,6.583247431,7.225001531\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.39403587,4.046461196,4.723040341,5.406190481,6.082029262,6.740481258,7.374869145\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.361979288,4.017466963,4.69661483,5.381929505,6.059628362,6.719728472,7.355630907\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.34907543,4.003993156,4.68265088,5.367616985,6.045123833,6.705177087,7.341153656\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.654788642,4.360784678,5.085997863,5.809963006,6.517792131,7.199553277,7.849327392\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,3.68499025,4.387475643,5.108646247,5.828421237,6.532193951,7.210213131,7.856659195\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.345220777,10.13223938,10.88866404,11.61278344,12.30331164,12.95941545,13.5807377\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.477140607,10.24341843,10.98356434,11.69481036,12.3750496,13.02282604,13.63731635\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,6.527251159,7.290417495,8.056783155,8.818521761,9.569056486,10.30281597,11.01518586\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.392017884,10.16901939,10.91766728,11.635684,12.32137108,12.97359721,13.59178966\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.411711692,10.1856095,10.9313843,11.64680101,12.33017408,12.98036838,13.59679633\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.485528135,10.12361237,10.76942422,11.4148722,12.05212575,12.67445075,13.27653639\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,7.805728142,8.545235347,9.281374879,10.01014781,10.72659572,11.42571958,12.10307321\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,6.535770601,7.316617073,8.09534479,8.864903382,9.619650793,10.35491149,11.06684168\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,7.884488274,8.616478523,9.345100047,10.06680596,10.77685397,11.47031405,12.14272494\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.527130519,10.16238745,10.8056803,11.44873131,12.08364324,12.70367617,13.30353858\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.348057049,10.13468917,10.89089687,11.6149143,12.30541354,12.96153073,13.5828873\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.47057116,10.2361425,10.97558843,11.68618945,12.36586726,13.01318024,13.6273094\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,6.52035242,7.285100835,8.052790252,8.815676917,9.567223473,10.30187702,11.01503266\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.387418794,10.16451058,10.91335657,11.63163866,12.31762659,12.97016482,13.58866283\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.408537362,10.18232605,10.92795867,11.64322356,12.32645189,12.97651969,13.5928459\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.481625652,10.11829639,10.76305311,11.40776528,12.04455052,12.6666213,13.26861789\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,7.810867525,8.54997665,9.285506437,10.01355746,10.72924403,11.42761751,12.10426427\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,6.543215354,7.322173576,8.099488642,8.867969551,9.621883453,10.3564936,11.06791318\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,7.885157849,8.616909637,9.345323071,10.06684888,10.77674283,11.47007295,12.14237588\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.530533345,10.16333514,10.80458848,11.44598909,12.07959741,12.69862554,13.29773451\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.713511249,10.45302959,11.19312061,11.92543532,12.6413732,13.33353828,13.99631034\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.973293675,10.69743704,11.41905733,12.13077709,12.82512084,13.49569686,14.13765563\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,10.10033237,10.80806721,11.51625934,12.21696044,12.90220344,13.56519327,14.20076016\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.72313946,10.46255624,11.20266848,11.93504575,12.65103649,13.34321657,14.00595349\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,9.972590567,10.69925007,11.42294173,12.13632339,12.83196284,13.50351622,14.14618245\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,10.08341916,10.79388431,11.50432035,12.20685945,12.89360538,13.55782445,14.19439877\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,14.00049174,14.82743646,15.57825324,16.25901272,16.87602954,17.43541711,17.94287981\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,14.4814642,15.26803717,15.98066461,16.62603938,17.21072476,17.7408382,18.22194482\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,15.39097924,16.06487378,16.66912687,17.21418962,17.70834135,18.15818024,18.56902362\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,15.53574968,16.20874996,16.81001856,17.351224,17.84120694,18.28680456,18.69342494\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,14.20528285,15.00446013,15.73278449,16.39505028,16.99666776,17.5430927,18.03954044\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,14.51399999,15.29477049,16.00281605,16.6445478,17.22631515,17.75407346,18.23326477\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,15.39896748,16.07153035,16.67492002,17.21940174,17.71314324,18.1626755,18.57327535\n\"linker [CH]1C=NN=N1, [N]1C=CN=N1, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology pcu\",,,15.27148902,15.97812566,16.60738328,17.17208359,17.68194662,18.14448724,18.56564192\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,19.97614731,20.14479863,20.27646251,20.38113281,20.46566667,20.53488789,20.59226544\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,19.97611233,20.14476911,20.27643728,20.38111101,20.46564766,20.53487117,20.59225063\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,2.974782002,3.421953878,3.909064885,4.427095946,4.966202712,5.517034928,6.071499998\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.538750798,4.207155854,4.898744494,5.594636913,6.280467629,6.946127896,7.585130722\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.190378068,3.837454008,4.51152449,5.194690226,5.87268082,6.535019417,7.174651759\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.064417805,3.525182254,4.024701639,4.553268238,5.100712048,5.657622852,6.216020006\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.190933933,3.826864472,4.491321394,5.166587704,5.838383492,6.496110813,7.132540277\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,2.974786169,3.421972374,3.909097705,4.427142262,4.966261123,5.517103701,6.071577266\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.064560654,3.525340654,4.024873579,4.553451151,5.100903102,5.657819186,6.216218888\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.190368221,3.837444181,4.511514466,5.194679929,5.872670261,6.535008656,7.174640876\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.298206962,3.955750733,4.638571818,5.328518238,6.011301642,6.676579832,7.317517348\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.416624831,4.07262598,4.751676539,5.436371199,6.113036822,6.771797799,7.406149613\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.416616224,4.072619235,4.75167161,5.436367945,6.113035052,6.771797299,7.406150176\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.298254328,3.955801584,4.638624888,5.328572503,6.01135629,6.676634233,7.317571027\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.346721723,4.031979415,4.741813269,5.456137925,6.159759335,6.842085613,7.496409675\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.346684505,4.031945598,4.741783456,5.456112351,6.159737962,6.842068219,7.496395932\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.538724701,4.20712764,4.898715265,5.594607498,6.280438616,6.946099684,7.585103567\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,3.1908762,3.826800102,4.491252264,5.166515491,5.838309616,6.496036431,7.132466303\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.500313595,10.26498529,11.00388727,11.71414049,12.39359091,13.04075973,13.65480916\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,8.801342747,9.466744263,10.13839913,10.80874162,11.47028314,12.11646395,12.74202724\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.500240938,10.2649219,11.00383195,11.71409223,12.39354883,13.04072306,13.6547772\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.591003223,10.34414869,11.08820673,11.81319822,12.51139672,13.17742402,13.80800453\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.41613965,10.19491978,10.94573176,11.66601675,12.35390321,13.00815832,13.62815598\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,7.819652047,8.562233618,9.302134137,10.03483878,10.75506039,11.45761388,12.13796655\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.456550054,10.22614845,10.96950836,11.68376544,12.3667841,13.01711205,13.63394399\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,7.819662121,8.562241535,9.302140388,10.03484369,10.75506421,11.45761678,12.13796869\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,8.801338589,9.466737674,10.13839069,10.80873192,11.4702727,12.11645318,12.74201646\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,8.994299052,9.6333071,10.28834468,10.94872661,11.60466077,12.24793462,12.87213979\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,6.668353529,7.432616123,8.202598225,8.969172117,9.724742343,10.46304729,11.17907156\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.450976965,10.22099151,10.96476986,11.67938316,12.3626953,13.01327339,13.63033256\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.416047399,10.19483769,10.94565818,11.6659504,12.35384305,13.00810353,13.62810586\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,6.668385769,7.432644391,8.202622741,8.969193226,9.724760425,10.46306271,11.17908467\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,7.870901024,8.603746752,9.335087664,10.06038024,10.7742787,11.47151162,12.14744218\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,6.598353328,7.357782868,8.121372223,8.881243073,9.630668874,10.36389647,11.07613581\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.456569961,10.22616588,10.9695239,11.68377952,12.36679702,13.01712404,13.63395521\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.450836627,10.22086295,10.96465231,11.67927588,12.36259754,13.01318439,13.63025157\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,8.994241804,9.633257526,10.28830214,10.94869052,11.60463054,12.24790968,12.87211957\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,9.591016807,10.34415948,11.08821472,11.81320363,12.51139987,13.17742525,13.80800419\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,6.598335821,7.357773121,8.121368692,8.881244546,9.630674364,10.36390516,11.07614703\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,7.870899286,8.603745683,9.335087535,10.06038122,10.77428083,11.4715149,12.14744652\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,10.84644081,11.56970804,12.28619176,12.98695109,13.66455337,14.31344669,14.92991806\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,10.35234443,11.06949803,11.78238933,12.4830957,13.16438506,13.8204249,14.44698073\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,10.84634373,11.56962488,12.28611996,12.98688842,13.66449801,14.31339717,14.92987323\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,8.741938635,9.436826399,10.12928728,10.81602777,11.49243725,12.15361623,12.79507444\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,8.741673496,9.436586587,10.12906918,10.8158282,11.49225352,12.15344614,12.79491621\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,10.35257846,11.06969927,11.78256215,12.4832439,13.164512,13.82053354,14.44707364\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,14.85871726,15.65759169,16.37531735,17.02130057,17.60356475,18.12906392,18.60389728\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,16.02660736,16.61875411,17.1543343,17.64146017,18.08652418,18.49460997,18.86981424\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,15.51480791,16.20247409,16.81681321,17.36965925,17.86992197,18.32448932,18.73883314\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,14.85840113,15.6572883,16.37503139,17.02103382,17.60331735,18.12883515,18.60368597\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,14.62733511,15.40653622,16.10911799,16.74379548,17.31817032,17.83884787,18.31157819\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,15.51530694,16.2028951,16.81717136,17.36996631,17.87018713,18.32471985,18.73903482\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,16.02663633,16.61878719,17.15436925,17.64149555,18.08655909,18.49464385,18.86984677\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], n1cnn(c1)CCn1ncnc1, nodes [Cd], topology \",,,14.62797862,15.40711422,16.10963962,16.74426829,17.31860059,17.83924085,18.31193832\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,15.26767035,16.3685835,17.29818094,18.08483206,18.75300105,19.32313546,19.81205599\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,14.37216298,15.42183028,16.33979667,17.14063564,17.83896684,18.44847238,18.9814472\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,15.26904401,16.3698688,17.29937242,18.08593079,18.75401155,19.32406392,19.81290921\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,14.37276143,15.42241158,16.34036054,17.14117971,17.83948867,18.44897021,18.98192006\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,10.81790611,11.81226662,12.74008039,13.59978985,14.39197981,15.11883785,15.78365821\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,10.9037272,11.90627148,12.84210034,13.70868114,14.50614216,15.2365629,15.90333484\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,10.81753952,11.81960282,12.75638181,13.6249999,14.42526366,15.15898146,15.8293314\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,10.81828096,11.81247449,12.74017402,13.59980568,14.39194302,15.11876594,15.78356336\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,10.90427571,11.90667326,12.8424008,13.70891217,14.50632576,15.23671397,15.90346343\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,10.81728736,11.81945332,12.75631678,13.62500177,14.42531691,15.15907308,15.82945086\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,2.969393757,3.590882599,4.243340959,4.909473074,5.575052808,6.229288787,6.864615063\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,2.819924409,3.468979866,4.148824902,4.840655381,5.529445721,6.204105959,6.857093382\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,2.895245177,3.534002038,4.202966626,4.88416888,5.563078174,6.228849969,6.874019848\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,3.191424221,3.831228008,4.495470133,5.16760051,5.834404676,6.486120877,7.116108746\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,3.281428614,3.909896577,4.563642567,5.226949434,5.886801445,6.533336099,7.159701141\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,3.066695569,3.728540176,4.415720672,5.110350126,5.798254793,6.469096661,7.115972797\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,2.969367658,3.590877221,4.243354146,4.909502432,5.575095866,6.229343138,6.864678466\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,2.819885177,3.468933109,4.148772164,4.840598286,5.529386031,6.204045598,6.857034428\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,2.895414171,3.534178003,4.203144307,4.884344346,5.563248687,6.229013756,6.874175878\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,3.191058827,3.830831985,4.495060904,5.167190728,5.834003063,6.485733124,7.115738312\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,3.281021428,3.909476615,4.563222861,5.226539284,5.886407,6.532961048,7.15934737\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,3.066517467,3.728338507,4.415504306,5.110126052,5.798028306,6.468871643,7.115752008\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,7.950497615,8.775589637,9.585242811,10.37515149,11.14085791,11.87834848,12.58441221\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.441583568,10.23226097,10.98996021,11.71431383,12.40468354,13.06051756,13.68156077\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.118885879,9.970676133,10.78030017,11.5480154,12.27420602,12.9594281,13.60447474\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,8.046257785,8.868083425,9.675370754,10.46401658,11.22934861,11.96701892,12.67350143\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.228495963,10.05699577,10.84645159,11.59701802,12.30881576,12.98207974,13.61727569\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.420230838,10.20863328,10.96447211,11.68713728,12.37593938,13.03035641,13.65018203\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,8.089720662,8.888005408,9.672543351,10.44022335,11.18696653,11.90869049,12.60189521\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.3838564,10.17218717,10.92770853,11.6503299,12.33953347,12.99479346,13.61582516\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.415557,10.24162861,11.02749479,11.7738632,12.48112517,13.14964729,13.77996276\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,7.950713113,8.77576729,9.585393218,10.37528211,11.14097396,11.87845357,12.58450885\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.440837254,10.23160024,10.98937541,11.71379615,12.40422501,13.06011104,13.68119987\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.119197471,9.970952502,10.78054163,11.54822394,12.27438447,12.95957964,13.6046026\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,8.046366372,8.868178643,9.675451669,10.46408363,11.22940293,11.96706199,12.67353478\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.228094824,10.05661114,10.84608875,11.59667961,12.30850264,12.98179157,13.61701142\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.422332189,10.21054574,10.96621386,11.6887254,12.37738962,13.03168311,13.65139808\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,8.090917331,8.889081442,9.673515453,10.44110623,11.18777276,11.90943056,12.60257783\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.384785554,10.17305675,10.92852495,11.65109858,12.34025892,12.99547943,13.61647479\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,9.416733981,10.2426914,11.02845457,11.77473061,12.48191006,13.15035863,13.78060865\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,14.13602267,14.9865807,15.7518528,16.4435237,17.07018092,17.63859827,18.1544765\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,12.43826231,13.49711907,14.45860676,15.32756943,16.11028063,16.81379041,17.44540112\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.20330743,14.18741441,15.07048659,15.8637787,16.57691083,17.21831792,17.79553114\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.4114274,14.37302438,15.23904902,16.01887805,16.720903,17.35278557,17.92158097\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.56098894,14.49323578,15.33576597,16.09703433,16.78447136,17.40488903,17.96464527\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.25647535,14.29144556,15.21311255,16.03440127,16.76677569,17.42042586,18.0044278\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,14.12993218,14.9809995,15.74672811,16.43880822,17.06583306,17.63458156,18.15075887\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,12.44083643,13.49945308,14.46072807,15.32950201,16.11204543,16.81540576,17.44688311\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.20502423,14.18883447,15.07166892,15.86477084,16.57775037,17.21903433,17.79614751\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.40327277,14.36524052,15.2316725,16.01192229,16.71436615,17.34665594,17.91584082\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.55825778,14.4906816,15.33337146,16.09478686,16.78236094,17.40290711,17.96278403\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.2795678,14.31232226,15.23198412,16.05148146,16.78226555,17.43450753,18.01726307\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.37585848,14.29963605,15.13832121,15.89952286,16.58975433,17.2150108,17.78098445\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.26013962,14.24517091,15.12968608,15.92425337,16.6381598,17.27973591,17.85653549\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.51291882,14.45402376,15.30882459,16.08316668,16.78295879,17.41425771,17.98314798\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.39115742,14.31310439,15.1501911,15.91000941,16.59904894,17.22327979,17.78837042\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.26388866,14.24883815,15.13323862,15.92766997,16.64142777,17.28284885,17.85949167\n\"linker [O]P(=O)(c1ccc(cc1)P(=O)([O])[O])[O], nodes [Al], topology pcu\",,,13.53020567,14.46955202,15.32281839,16.0958199,16.79443769,17.42470459,17.99268487\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.44530925,16.53260305,17.44771181,18.22002239,18.87456342,19.43206257,19.90944789\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.44589933,16.53315941,17.44824593,18.22054379,18.87507928,19.43257797,19.90996629\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.43553548,16.52253671,17.43721968,18.20904201,18.86307626,19.42007624,19.89698467\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.43471351,16.52160958,17.43617093,18.20787012,18.86178711,19.41867895,19.89548938\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.305114392,3.964282041,4.646986163,5.335578724,6.016228811,6.678959357,7.31720064\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.306869266,3.966214841,4.649029879,5.337677753,6.018339371,6.681048386,7.31924411\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.301619667,3.960866059,4.643553107,5.332062907,6.012588517,6.675170702,7.313252378\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.298306452,3.95748958,4.640169785,5.328716854,6.009311453,6.67198363,7.3101678\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.298824909,3.958001895,4.640663432,5.329184599,6.009750037,6.672392534,7.310548241\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.301890564,3.961124707,4.643807624,5.332319253,6.012850793,6.67544153,7.313533265\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.30703329,3.966322599,4.649086705,5.337690253,6.018314749,6.680993855,7.319166482\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.30479334,3.963972776,4.646690996,5.335298788,6.015964094,6.678708969,7.316963125\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.398310196,7.911915111,8.408308896,8.88163024,9.32766587,9.744019115,10.12984997\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.426396804,7.939914041,8.436247196,8.90952736,9.355535719,9.771871594,10.15769209\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.211170448,7.726730606,8.224660376,8.699194046,9.146191034,9.563310322,9.949754683\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.105883485,7.617491898,8.112316843,8.584399298,9.029451666,9.445020438,9.830221999\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.500518138,4.181114222,4.880846366,5.581992368,6.270985793,6.938307489,7.577927996\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.508482324,4.18893916,4.888527632,5.58953708,6.278408012,6.945624569,7.58515808\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.508948001,4.189398701,4.888977157,5.589975209,6.278835038,6.946041769,7.585567204\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,3.499978011,4.18055229,4.880265498,5.581395434,6.270375488,6.937686237,7.577297911\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.329723541,7.121498662,7.904890508,8.674880302,9.427535699,10.15952193,10.86797359\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.578833828,8.365789629,9.138013814,9.8932793,10.62869572,11.34117794,12.02786583\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.182726654,9.958339499,10.71192968,11.43947558,12.13753081,12.80355051,13.4359431\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.330728751,7.122650457,7.906166056,8.676250986,9.428973827,10.16100359,10.86947946\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.579159086,8.36613398,9.138356483,9.893608711,10.62900718,11.34147145,12.02814423\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.181681032,9.957307356,10.71089596,11.43843529,12.13648502,12.80250361,13.43490103\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.364058936,7.155043111,7.937580262,8.706701709,9.458511025,10.18969629,10.8974047\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.596966823,8.383911808,9.156093909,9.911295128,10.6466349,11.35903625,12.04564497\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.097305891,9.872893213,10.62635708,11.35372577,12.05158434,12.71740646,13.34961068\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.361356481,7.151988632,7.934301426,8.703292725,9.455039436,10.1862091,10.89393357\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.593016161,8.379902767,9.152021349,9.907158685,10.64243731,11.35478211,12.04133983\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.088292006,9.863969592,10.6174878,11.3448906,12.04277336,12.70861607,13.34084086\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.356977078,7.147593529,7.929901253,8.698888777,9.450629495,10.18179034,10.8895038\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.575761423,8.362771212,9.134999181,9.890232638,10.62559507,11.33801252,12.02463298\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.073446298,9.849326645,10.60302872,11.33059481,12.02861972,12.69458394,13.32691089\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.360063487,7.150830203,7.933186578,8.702161073,9.453853292,10.18494697,10.89258508\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.581214882,8.368071342,9.140172887,9.89530263,10.6305807,11.34293037,12.02949715\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.084666995,9.860106043,10.61343579,11.34068765,12.03844795,12.7041901,13.33633147\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.335969272,7.127615172,7.910853426,8.680677072,9.433163775,10.164986,10.87328298\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.594059788,8.380942729,9.153100562,9.908307554,10.64367366,11.35611348,12.04276624\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.196468642,9.972199644,10.7258894,11.45351844,12.15164259,12.81771911,13.45015844\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,6.33327289,7.12550961,7.909307962,8.679649141,9.43260421,10.16484373,10.87350836\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.595871852,8.382876285,9.155116369,9.910376829,10.64577679,11.35823802,12.04490496\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.196977814,9.972462095,10.72592962,11.45336566,12.15132711,12.81727001,13.44960227\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.164468429,9.949012153,10.7109917,11.44591216,12.15014713,12.82114518,13.45740093\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.286715288,8.112092481,8.918130453,9.702152085,10.46159471,11.19399514,11.89716843\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.236725464,10.02087865,10.78241486,11.51687326,12.2206524,12.89121697,13.52707082\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.141365685,7.966731394,8.772584729,9.556303251,10.31536118,11.04732059,11.75001447\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.22343974,10.00765614,10.76924887,11.50375892,12.20758615,12.87819614,13.5140933\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.131713545,7.957088234,8.762948321,9.546672474,10.30573539,11.03769931,11.74039724\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,9.17648165,9.960955417,10.72286931,11.4577284,12.16190637,12.83285183,13.4690594\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,7.297157387,8.122521786,8.928550586,9.712565799,10.47200403,11.20440152,11.90757288\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.65301753,14.49305473,15.24592893,15.92279288,16.53317558,17.08515722,17.58558761\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.93294991,14.75421539,15.49057416,16.15301352,16.75093871,17.29231249,17.78385551\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.64486603,14.48420807,15.23675631,15.91353602,16.5239897,17.07613936,17.5767959\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.91700509,14.73859257,15.47533924,16.13818995,16.73652416,17.2782899,17.77020021\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.79111029,14.63663959,15.39403544,16.07460814,16.68803218,17.2425132,17.74500516\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.89519255,14.71748649,15.45458697,16.11755052,16.7158387,17.2574576,17.74916032\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.80676795,14.64698773,15.39997773,16.07686212,16.68717063,17.23899655,17.73920652\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.90476448,14.72687012,15.46377049,16.12653721,16.72463972,17.26608771,17.75763545\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.71857977,14.55794767,15.31030573,15.98671626,16.59666732,17.14822353,17.64823113\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.85755388,14.67966013,15.41660898,16.07944766,16.67763149,17.21916221,17.71078979\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.7146816,14.55859107,15.31450812,15.99374475,16.60596752,17.15937005,17.66089329\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.85256808,14.67422715,15.41080716,16.07334171,16.67127396,17.21259543,17.70404776\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.74638192,14.58509225,15.33700119,16.01314716,16.62298392,17.17454172,17.67463675\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.97262879,14.79419671,15.5308405,16.19354256,16.79170601,17.33329331,17.82502603\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.72540584,14.56801231,15.32331038,16.00242827,16.61488731,17.16877043,17.67093597\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,13.95309869,14.77573546,15.51332823,16.17687148,16.77578027,17.31802846,17.81034813\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.72790543,16.67446347,17.47236798,18.1478451,18.7225813,19.21424422,19.63714255\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.75233047,16.69707579,17.49348555,18.16772235,18.74142193,19.23221205,19.65437017\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.70249479,16.64917509,17.44713354,18.12262342,18.69734785,19.18898475,19.61184922\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Al], [OH], topology \",,,15.7010522,16.64708679,17.44455208,18.11966146,18.69408932,19.18549281,19.60817185\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,20.28471654,20.6542213,20.94447981,21.17633615,21.36430544,21.5187091,21.64703043\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,20.285048,20.65450271,20.94472118,21.17654514,21.36448794,21.51886971,21.64717278\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,20.28416642,20.6537491,20.94407117,21.17597972,21.36399226,21.51843203,21.64678376\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,20.28486294,20.65434294,20.94458232,21.17642362,21.36438089,21.51877481,21.64708815\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.410232872,4.08104498,4.778010481,5.481139193,6.175165256,6.849324989,7.496693625\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.568351173,4.237795299,4.929916202,5.62582903,6.311217307,6.976041691,7.61388593\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.410207715,4.081016627,4.777979897,5.481107284,6.175132802,6.84929262,7.496661825\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.568417072,4.237856849,4.929973559,5.625882388,6.311266892,6.976087737,7.613928661\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.409937001,4.080723543,4.777668326,5.480781714,6.174797792,6.848952457,7.496320333\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.568535884,4.238019674,4.930174104,5.626113914,6.311522719,6.976361626,7.614215031\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.410074713,4.080862723,4.777807848,5.480920441,6.174934681,6.849086601,7.496450976\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,3.568482539,4.237948288,4.930087549,5.626015161,6.311414636,6.976246837,7.614095843\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,7.320897107,8.060386137,8.787725312,9.500988165,10.19808945,10.87676108,11.53472166\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.980742199,9.612334112,10.25704592,10.90639155,11.55185986,12.18590559,12.80239775\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.981144666,9.606961779,10.24745087,10.89372661,11.53699081,12.16949075,12.78494269\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,7.320861746,8.06035035,8.787689362,9.500952378,10.19805414,10.87672651,11.53468804\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.980777922,9.612368594,10.25707902,10.90642331,11.5518904,12.18593502,12.80242618\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.981219003,9.60703001,10.24751842,10.8937968,11.53706539,12.16957035,12.78502724\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,7.320895838,8.060383291,8.787720754,9.500981861,10.19808146,10.87675152,11.53471072\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.980776539,9.612352932,10.25704109,10.90635903,11.55179867,12.18581685,12.80228388\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.980996015,9.606861161,10.24739425,10.8937094,11.53700805,12.16953739,12.78501383\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,7.320868459,8.060355122,8.78769149,9.50095146,10.19805003,10.87671926,11.53467785\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.980807606,9.612391663,10.25709484,10.90643177,11.55189178,12.18592989,12.80241524\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,8.981083652,9.606927328,10.24744274,10.89374348,11.53703053,12.16955067,12.78501994\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.36033691,11.04694398,11.73195217,12.40901584,13.07134285,13.71290427,14.32896153\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.20571799,10.92924736,11.64907485,12.35780502,13.04805456,13.71359654,14.34978142\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.37128212,11.09215565,11.80868204,12.5133219,13.1987422,13.85886127,14.48920595\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.36027688,11.04690774,11.73193653,12.40901763,13.07135905,13.7129321,14.32899854\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.2056956,10.92922132,11.64904682,12.35777648,13.04802667,13.71357017,14.34975713\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.37120625,11.09209616,11.80863663,12.5132887,13.19871957,13.85884773,14.48920018\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.36023374,11.04687013,11.73190914,12.40900292,13.07135785,13.71294416,14.32902289\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.20546656,10.92901066,11.64884424,12.35757511,13.04782245,13.7133611,14.34954268\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.371341,11.09218665,11.80868473,12.51329769,13.19869363,13.85879147,14.48911826\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.36023496,11.0468722,11.73190735,12.40899454,13.07134163,13.71291984,14.32899087\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.20547993,10.92905183,11.64891442,12.35767359,13.04794707,13.7135088,14.34970998\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,10.37134063,11.09219582,11.80870677,12.51333414,13.19874465,13.85885629,14.48919551\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,15.24423378,15.95639712,16.59041758,17.15852686,17.67048208,18.13407197,18.55555436\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,14.72994144,15.48353126,16.16251145,16.77573225,17.33093704,17.83479531,18.29302742\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,15.243918,15.95613514,16.5902,17.15834625,17.67033245,18.13394836,18.55545267\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,14.7302639,15.48379785,16.16273279,16.77591662,17.33109094,17.83492395,18.29313503\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,15.24427501,15.95643205,16.59044674,17.15855084,17.67050147,18.13408734,18.55556624\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,14.72994092,15.48353186,16.1625126,16.77573364,17.33093848,17.83479669,18.29302869\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,15.2439596,15.95616884,16.59022671,17.15836685,17.67034776,18.13395914,18.55545958\n\"linker [N]1=CN=NC=1, [O-]C(=O)C(=O)[O-], nodes [Zn], topology \",,,14.73023274,15.48377205,16.16271069,16.77589708,17.33107322,17.83490754,18.2931196\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,18.98952586,19.51617949,19.9361861,20.27580002,20.5538879,20.78420768,20.97694205\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,19.07234534,19.58828344,19.99924967,20.33125232,20.60291951,20.82780101,21.01590577\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.293251498,3.986349449,4.696090329,5.405378443,6.101317383,6.774951901,7.420670988\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.577049379,4.279312685,4.995623829,5.708415842,6.404814813,7.076124666,7.717079265\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.790434161,4.51041201,5.238794038,5.958669025,6.65798673,7.328892727,7.966898173\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.313547859,4.009877278,4.722313324,5.433705992,6.131156262,6.805741098,7.451901627\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.628170272,4.335438025,5.055370801,5.770519391,6.468184854,7.139861901,7.780467315\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.801161687,4.522491977,5.251975508,5.972695299,6.672613481,7.343899185,7.982092671\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.294502049,3.987624037,4.697323762,5.406531376,6.102369273,6.775894995,7.42150573\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.596066545,4.299416999,5.016331099,5.72931803,6.425590044,7.096531937,7.736946741\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.79464185,4.514353823,5.24250462,5.962169012,6.661289756,7.332009183,7.969837117\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.313392697,4.009293502,4.721383096,5.432505684,6.12975523,6.804201487,7.450278718\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.620762497,4.327206888,5.04656036,5.761345088,6.458827019,7.130465325,7.771144209\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,3.798898485,4.519901043,5.249177522,5.969787722,6.669670409,7.340974618,7.979224598\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.056991235,9.884075602,10.67419667,11.42607209,12.1391725,12.8135131,13.44954592\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.545694337,8.378591177,9.185791893,9.967140352,10.72152737,11.44732218,12.14283498\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.190279052,8.017323058,8.830181117,9.623572263,10.39314101,11.13531852,11.84731854\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.771117783,8.511157032,9.241560626,9.96069847,10.66558123,11.3526648,12.0184758\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.024943423,9.75488183,10.4763513,11.18357827,11.87095759,12.53375091,13.16837362\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.021899216,9.761364493,10.49048267,11.20382135,11.89603163,12.56258252,13.20006466\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.060984541,9.889338688,10.68046663,11.43315303,12.14690313,12.82175253,13.45816818\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.552999482,8.386486396,9.194558608,9.976893418,10.73225512,11.45892993,12.15518202\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.198951757,8.028081389,8.842993576,9.638300551,10.4095743,11.15320496,11.86639083\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.784187651,8.527892435,9.26200572,9.984706176,10.69285433,11.38280672,12.05103803\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.043780807,9.778105853,10.50352736,11.21417819,11.90440598,12.56946719,13.20580372\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.025305389,9.768871679,10.50189889,11.21879351,11.91410979,12.58327489,13.22287869\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.044165195,9.871231207,10.66116517,11.41276716,12.12557194,12.79964012,13.43545273\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.54339397,8.375211775,9.181008153,9.960838961,10.71374309,11.43818285,12.13251907\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.18604054,8.014221994,8.828257132,9.622806983,10.3934702,11.1366465,11.84953161\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.783610646,8.52303986,9.252969779,9.971731084,10.67629995,11.36310564,12.02865607\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.040487762,9.769321049,10.48972322,11.1959332,11.88235646,12.54426114,13.17806512\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.036777628,9.773930429,10.50111001,11.21281566,11.90364698,12.56903236,13.20552922\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.068256042,9.895834324,10.68619934,11.43814676,12.15119699,12.82539801,13.46122447\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.554430865,8.388763533,9.197056029,9.979207111,10.73414649,11.46027774,12.15594419\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.191113077,8.020226662,8.835127205,9.630438159,10.40173871,11.14542277,11.85868964\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,7.787401161,8.530031738,9.263109831,9.98484089,10.69210548,11.38127241,12.04882156\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.051937006,9.784334292,10.50796324,11.21698036,11.90575151,12.56954118,13.20478949\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.028520125,9.771694815,10.50426807,11.22069687,11.91556515,12.58431668,13.22354952\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.86340424,10.66203242,11.44396864,12.20326622,12.93415034,13.63195762,14.29346126\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.731102096,10.56715389,11.38208261,12.16951814,12.92378029,13.64059233,14.31724841\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.878339962,10.6788312,11.46239417,12.22307711,12.95509445,13.65377967,14.3159137\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.74026295,10.57687031,11.39254396,12.18080611,12.93588764,13.6534478,14.330741\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.889878394,10.68610886,11.46583596,12.22312142,12.95218881,13.64836575,14.30841192\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.746074264,10.57981025,11.39262364,12.17817088,12.93077942,13.6461656,14.32160728\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.890410961,10.68813628,11.46915858,12.22757606,12.95762317,13.65463102,14.31536344\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,9.68313461,10.52481377,11.34503343,12.13735354,12.89605244,13.61683874,14.29701383\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,14.97147961,15.93452315,16.76633243,17.48808351,18.11715289,18.66780069,19.15177255\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,15.23263468,16.16522454,16.97214324,17.67313275,18.2845889,18.8200887,19.29088975\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,14.83304504,15.80706818,16.64899295,17.37997471,18.01742993,18.57568218,19.06654685\n\"linker Fc1cc(C2=CN=N[CH]2)c(cc1C1=CN=N[CH]1)F, nodes [Co], topology pcu\",,,14.85644734,15.83193141,16.67507066,17.40689511,18.04480446,18.60315849,19.09382994\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,20.68084759,21.09313546,21.41959314,21.68203042,21.89586707,22.07221752,22.21923584\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,20.5735876,21.00216066,21.34159938,21.61451346,21.8369062,22.02032139,22.17323245\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,20.64353735,21.06139472,21.39231709,21.65837357,21.8751762,22.05398254,22.20305408\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,20.67814195,21.09082897,21.41760848,21.68030765,21.89435946,22.07088838,22.21805606\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,20.54040413,20.97404978,21.31752282,21.59368719,21.81873058,22.00433187,22.15906463\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,20.64863628,21.06571061,21.3960132,21.66157164,21.87796861,22.05644053,22.20523337\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,3.381604706,4.071092524,4.77713197,5.482705809,6.17492581,6.844804356,7.486679621\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,3.381631785,4.0711275,4.777199265,5.482817612,6.175085719,6.845010584,7.486927406\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,3.378353109,4.067484408,4.773298727,5.478749099,6.170922931,6.840813098,7.482742373\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,3.381811069,4.071312395,4.777362189,5.482942682,6.175165794,6.845044379,7.486917187\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,3.38157387,4.07108601,4.777172337,5.482803355,6.175082269,6.845016169,7.486940389\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,3.379024353,4.068258097,4.774147926,5.479649077,6.171852564,6.841755199,7.483683468\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,6.668764867,7.476220018,8.276202029,9.063323618,9.832888513,10.58073111,11.30328562\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.730335463,8.531299559,9.322139964,10.09830023,10.85491205,11.58744835,12.29213004\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.364142965,8.225233886,9.066787221,9.885177093,10.67684232,11.43851567,12.1674944\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,9.238434166,10.0575961,10.84401808,11.59524453,12.30974659,12.98674788,13.62610671\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,6.668660148,7.476189579,8.276149118,9.063204761,9.832689674,10.58045366,11.30293826\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.72945688,8.530510666,9.321428217,10.09765498,10.85432405,11.58690967,12.29163403\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.366196339,8.22749049,9.069245671,9.88782355,10.67965135,11.44145472,12.17052831\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,9.235909419,10.05539744,10.84212221,11.59361903,12.30835662,12.98555978,13.62508982\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,6.675044184,7.480075832,8.278144716,9.063792394,9.832246085,10.57926884,11.30123294\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.723383244,8.524404863,9.315384252,10.09173128,10.84855735,11.58132289,12.28624088\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.350079399,8.211577759,9.053752008,9.872874274,10.66531447,11.42776165,12.15748703\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,9.233574975,10.05271063,10.83926765,11.59071854,12.30548937,12.98277575,13.62241906\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,6.67052929,7.477612928,8.277284841,9.064151242,9.833508433,10.58118343,11.30360363\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.73022274,8.531186921,9.322029912,10.0981949,10.85481296,11.58735639,12.2920456\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.363798367,8.225007835,9.066669921,9.885156317,10.67690488,11.43864849,12.16768516\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,9.238979372,10.05808852,10.84447538,11.59567779,12.31016261,12.98715066,13.62649847\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,6.670404407,7.477645883,8.277357299,9.064202593,9.83351159,10.58112999,11.303495\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.729214904,8.530249219,9.321156372,10.0973788,10.85404759,11.58663567,12.29136437\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.365862883,8.227280264,9.069132574,9.887787376,10.67967614,11.44152765,12.17063901\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,9.235666933,10.05530866,10.84215988,11.59375956,12.30857984,12.98584856,13.6254297\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,6.674513598,7.479561644,8.277655868,9.063331825,9.831813714,10.57886321,11.30085211\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.723248752,8.524280482,9.315277891,10.09164682,10.84849602,11.58128424,12.28622343\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,7.34987476,8.211369841,9.053556978,9.872702075,10.66517036,11.42764753,12.15740257\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,9.233606973,10.05278958,10.83938776,11.59087345,12.3056727,12.98298152,13.62264191\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.17778042,14.99738403,15.73937436,16.41155677,17.02105891,17.57428604,18.07695946\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.68160708,15.47040497,16.17829745,16.81548349,17.39066642,17.91122602,18.38343015\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.23814768,15.22273804,16.08874528,16.85209601,17.52669858,18.12450481,18.65572411\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.12014876,14.94314238,15.68871577,16.36446072,16.97738465,17.53383047,18.03949235\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.68403334,15.47622133,16.18626734,16.82477366,17.40071235,17.92164362,18.39395782\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.19518938,15.1848556,16.05542414,16.8227895,17.50088359,18.10170682,18.63552537\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.1064379,14.93058374,15.67755954,16.35474093,16.96902233,17.52669514,18.03343686\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.76943441,15.55461614,16.25830097,16.89107221,17.46185177,17.97814089,18.44627203\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.15740862,15.14602629,16.01670776,16.78491227,17.4642843,18.0666347,18.60210483\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.16525344,14.98633544,15.72959124,16.40285985,17.0132965,17.56732972,18.07070053\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.70067357,15.48787601,16.1943181,16.83019408,17.40419742,17.9236959,18.39494517\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.22526418,15.21144364,16.07877933,16.84324815,17.5187985,18.11741385,18.64932855\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.10752949,14.9315488,15.67807835,16.35470284,16.9684287,17.52560154,18.03192036\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.72279693,15.51092304,16.21747073,16.85294943,17.42625579,17.94488796,18.41518505\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.16192523,15.15534608,16.02915653,16.79931687,17.47982335,18.08273419,18.61836558\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.1243267,14.94712461,15.69273757,16.36860871,16.98166712,17.53821883,18.04394428\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.77182752,15.5565571,16.25990499,16.89242078,17.4630034,17.97913823,18.44714659\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology nbo\",,,14.19157983,15.17752525,16.04556343,16.81126903,17.4883376,18.08859523,18.62217961\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,18.54128712,18.94110631,19.26132897,19.5212437,19.73476195,19.91208419,20.06080505\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,18.44762688,18.86421838,19.19715833,19.46691585,19.68819315,19.87173238,20.02550734\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.311543544,3.989193205,4.675076137,5.355728419,6.021443551,6.665805481,7.285060376\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.010287798,3.627116604,4.25993078,4.896637822,5.527787849,6.146516279,6.748224015\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.310311199,3.987830372,4.673641554,5.354256808,6.019955256,6.664312308,7.28356897\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.011339049,3.628201388,4.261065225,4.897822938,5.529015698,6.147774341,6.749498051\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.310527788,3.988211227,4.674141819,5.354847683,6.020617311,6.66503167,7.284335255\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.007981936,3.624700228,4.257468085,4.894178376,5.52536853,6.144163696,6.745956802\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.309562857,3.987056671,4.672870994,5.353509989,6.01924602,6.663649218,7.282956721\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,3.011034726,3.627862714,4.260697484,4.89743115,5.528604756,6.147348972,6.749062713\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,6.230294001,6.997003852,7.767191269,8.533409236,9.288995843,10.02810837,10.74583191\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.375947964,10.14812638,10.8772034,11.56588568,12.2165553,12.83131148,13.4120146\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.60423121,10.3402171,11.02888618,11.67700961,12.28949322,12.86979773,13.42035448\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,6.226216362,6.993552885,7.76429448,8.530995472,9.286996919,10.02646141,10.74448082\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.379511972,10.15060838,10.87891975,11.56705649,12.21733406,12.83180601,13.41230142\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.605118846,10.34028422,11.0284226,11.67621723,12.28851084,12.86871932,13.41924258\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,6.229479856,6.996376397,7.766717316,8.533062337,9.288754279,10.02795396,10.7457493\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.375670559,10.14789238,10.87699404,11.56569021,12.21636786,12.83112898,13.41183552\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.604061371,10.34005832,11.0287415,11.67688124,12.28938243,12.86970491,13.42027931\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,6.2268563,6.994109845,7.764785263,8.53143259,9.287389795,10.02681723,10.74480515\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.380140655,10.15118087,10.87945137,11.56755707,12.21781002,12.83226159,13.41273948\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,9.605847182,10.34095598,11.02903787,11.67677792,12.28902014,12.8691812,13.41966133\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,14.63008306,15.42848349,16.13498791,16.76420859,17.32743186,17.83358006,18.28987726\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,12.63804912,13.54608363,14.35914921,15.08968326,15.74822555,16.3436473,16.88342509\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,14.48496471,15.29891402,16.01896522,16.65996003,17.23342134,17.74849045,18.21258423\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,12.72447179,13.62327964,14.42821614,15.15163663,15.80396955,16.39397127,16.9290111\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,14.62956752,15.42818321,16.1348719,16.76424584,17.32759357,17.83384067,18.29021478\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,12.61637218,13.52655552,14.34152649,15.07373892,15.73375647,16.33047545,16.87139609\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,14.49211302,15.30530472,16.02469488,16.66511483,17.23807618,17.75270958,18.21642243\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Ni], topology pcu\",,,12.73175113,13.62990351,14.43424303,15.15712558,15.80897649,16.39854747,16.93320269\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,17.40647629,18.27852719,19.00183025,19.60565928,20.11325062,20.54292901,20.90913981\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,17.74988846,18.55107041,19.21662629,19.77420255,20.24509,20.64577427,20.98911894\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,18.07148638,18.73952057,19.28614482,19.73885283,20.11831119,20.44013983,20.71621832\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,17.40952745,18.26999674,18.98639019,19.58623005,20.09164624,20.52027212,20.88612306\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,17.42881622,18.2698345,18.96941626,19.5555863,20.05031509,20.47083626,20.83071868\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,17.30631898,18.17417744,18.89714748,19.50307775,20.01423458,20.44829637,20.81928486\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.409800191,4.061915826,4.736266582,5.415941111,6.087706031,6.742003086,7.372517683\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.386487786,4.031821543,4.700008762,5.374429395,6.041964615,6.693049525,7.321290492\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.368002229,4.012153508,4.679365922,5.353061179,6.020128307,6.670987486,7.299217298\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.446283865,4.099926664,4.775965018,5.457383739,6.130784995,6.786460328,7.417987871\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.405525701,4.055708602,4.729697021,5.410280725,6.083810374,6.740329724,7.373201551\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.370936143,4.02991306,4.711301456,5.397845438,6.076034847,6.736132578,7.3717356\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.407427785,4.057998663,4.730886554,5.409269043,6.079953551,6.733390617,7.363255083\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.447817386,4.104829053,4.784100733,5.468426297,6.144307008,6.80200147,7.435099969\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.374029382,4.030189391,4.709521311,5.394673676,6.072002394,6.731637597,7.367062049\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.401695316,4.068405831,4.75792387,5.452245913,6.137359303,6.803243131,7.443378291\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.438408138,4.0937923,4.771757093,5.455126516,6.130379816,6.78772973,7.420713785\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.414834362,4.065658465,4.738525195,5.416694268,6.087042137,6.740071904,7.369495763\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.453280415,4.109053951,4.787024709,5.470098663,6.144842932,6.801548145,7.433813782\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.36477914,4.019629314,4.697907638,5.382262569,6.059032492,6.718320074,7.35357654\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.363958093,4.028327406,4.716486882,5.41027287,6.095504722,6.762006052,7.403123787\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.405693665,4.05553244,4.727609977,5.405201366,6.075173715,6.728007464,7.357386708\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.441272542,4.098024987,4.777189932,5.461550538,6.137580203,6.795505815,7.428888796\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.395274505,4.044736454,4.718252275,5.398583792,6.072046126,6.728646137,7.361712188\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.344737063,4.001016303,4.680269904,5.365244555,6.042394794,6.701924422,7.337360329\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.401212746,4.067225666,4.756066589,5.449753124,6.134291615,6.799674648,7.439390154\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.418652724,4.088435703,4.780140972,5.475875883,6.161761636,6.827911148,7.467926216\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.379623605,4.040110664,4.723795118,5.413000608,6.093887756,6.756496121,7.394292027\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.353975406,4.007497969,4.684533197,5.367817275,6.043737009,6.702410507,7.337281192\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.415161549,4.064367689,4.736201517,5.413787912,6.083879063,6.736876141,7.366413207\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.387950756,4.034740654,4.704500374,5.38044503,6.049354913,6.701615057,7.330816763\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.371541528,4.028234028,4.708171666,5.393918245,6.071788111,6.731894928,7.367718705\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.362239446,4.018678472,4.698109928,5.383233349,6.060469634,6.720004994,7.355361682\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,3.433645417,4.088076038,4.765111999,5.447620242,6.122120338,6.778850908,7.411359705\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.434170951,10.22107559,10.98595534,11.72393882,12.43114559,13.10486179,13.74348877\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.479119998,10.26175421,11.02109839,11.75321779,12.45477407,13.12333723,13.75743148\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.546512268,8.376198695,9.189276904,9.981657507,10.74976399,11.49046106,12.20115875\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.564779517,8.39621264,9.210701351,10.00422903,10.77325164,11.51464958,12.22584461\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.515555223,10.29272484,11.0478495,11.77667602,12.47562587,13.14209126,13.77446636\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.718875707,10.48715767,11.22884655,11.94124233,12.62230784,13.27066116,13.88555035\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.7003443,8.485710371,9.262892249,10.02732695,10.77428531,11.49932947,12.19866421\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,8.126373769,8.866675826,9.600084002,10.32391104,11.03421398,11.72672689,12.39749925\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.847147312,8.630903091,9.400586996,10.15356963,10.88680415,11.59716967,12.28182056\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.881742715,8.677657471,9.457157141,10.21808786,10.95771191,11.67312076,12.3616315\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.719677815,8.504222254,9.280224713,10.04327713,10.78877351,11.51236331,12.21030765\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.578072193,7.361083611,8.14179725,8.914499578,9.674002142,10.41558039,11.13510172\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.491914391,10.26848552,11.02401246,11.75363361,12.45346143,13.12074971,13.75384443\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.581229838,7.396697435,8.204863258,9.000357267,9.778408067,10.53474978,11.26571951\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.772783627,10.54550002,11.29017696,12.0045342,12.68680274,13.3357722,13.95080606\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,8.098976596,8.838002924,9.571260272,10.2956094,11.00681914,11.70044319,12.37241973\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.529646207,8.35966139,9.172977367,9.965608516,10.73402548,11.4751066,12.18625736\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.72989561,8.516345328,9.294143906,10.05887588,10.80589746,11.53082069,12.22988214\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.791292342,10.55873281,11.29819522,12.00760539,12.6853362,13.33025992,13.94177457\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.683967519,10.4507227,11.19120588,11.90265263,12.58302049,13.23093219,13.84563289\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.718398029,10.48485304,11.22468252,11.93521372,12.61447738,13.26115766,13.87455066\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.826108405,10.59066767,11.32796541,12.03578736,12.71235108,13.35639283,13.96720448\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,17.76371908,18.27085239,18.73378636,19.15837107,19.54852383,19.90720802,20.23692324\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.715205799,10.4828243,11.22374453,11.93524311,12.61533461,13.26270366,13.87665516\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.862527296,8.66032599,9.442289828,10.20595518,10.94835799,11.66643711,12.35741596\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.494908565,10.27520254,11.03229479,11.76222813,12.46167945,13.12824719,13.76048362\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,17.77217461,18.27957745,18.74259293,19.16711022,19.55708847,19.9155264,20.2449507\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.500035299,10.28019576,11.03811652,11.76954404,12.47087574,13.13948233,13.77374781\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,8.119901072,8.861513033,9.596321392,10.32153795,11.03315079,11.72685173,12.39866889\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.560713423,8.392643714,9.20782661,10.00214858,10.77199035,11.51417962,12.22610485\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.590832806,7.395785332,8.195164361,8.983508651,9.755884046,10.5078326,11.23549718\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.464175671,10.24982279,11.01184285,11.74629713,12.44985981,13.12012416,13.75564356\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.739980932,8.525305145,9.302075689,10.06587287,10.81205114,11.53622022,12.2346128\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.876989428,8.660002965,9.428936463,10.1811784,10.91368026,11.62331385,12.30722689\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.764469491,10.53628953,11.28002541,11.99348178,12.67494555,13.32323827,13.93773696\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.792281945,10.5607417,11.30142224,12.01209383,12.69103124,13.33704874,13.94951425\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.676465885,10.44219767,11.1817607,11.89239717,12.57207181,13.21941185,13.8336627\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.490512712,7.299792439,8.104750306,8.899318242,9.678144703,10.43649336,11.17032762\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.492686751,10.27548548,11.035782,11.76930254,12.47244062,13.14257605,13.77811096\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.629880039,7.428718077,8.222197092,9.005082835,9.772551742,10.52018192,11.24410681\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.454066267,10.22154912,10.9687409,11.69105602,12.38474243,13.04708434,13.67638493\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.481079932,10.2637604,11.02340693,11.75595673,12.4579702,13.12695158,13.76138964\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.737502502,10.50660185,11.24785639,11.9591228,12.63873562,13.28554453,13.89893239\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.779925136,7.554656811,8.324552083,9.085407025,9.832951501,10.56299928,11.27170991\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,10.18546343,10.98651274,11.72584206,12.41268448,13.05428773,13.65619937,14.22261224\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.767576863,10.53444626,11.27393517,11.98379185,12.66225613,13.30810089,13.92065031\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.840229681,8.640910265,9.425733694,10.19213938,10.9370912,11.65748409,12.35052177\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.804214849,10.56875663,11.30574475,12.01308137,12.68909734,13.33261775,13.94299451\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.478569693,10.25622035,11.01288319,11.74365713,12.44461784,13.11299032,13.74710084\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.727435974,10.4954385,11.23678695,11.94871368,12.62919539,13.27689029,13.89108832\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.496041933,10.27487353,11.03110145,11.76073036,12.4603238,13.12735133,13.76024825\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.611644169,7.403574676,8.194327692,8.977464227,9.747187103,10.49831066,11.22639122\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.798976603,7.567951801,8.333319762,9.090613053,9.835360413,10.56321997,11.27022909\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.51435163,7.262258159,8.006819006,8.742294923,9.463919185,10.16769753,10.85034999\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.845840883,8.621013559,9.383156867,10.12966807,10.85746248,11.56334654,12.24438485\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.696039877,10.4682192,11.21359957,11.9293517,12.61338983,13.26432736,13.88143125\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.599728343,7.408597458,8.209929491,8.998803017,9.770725324,10.52158535,11.24778803\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,9.692501115,10.46320067,11.2071335,11.9215591,12.60443867,13.25440499,13.87072654\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,8.088748108,8.831569026,9.567796314,10.29450126,11.00759453,11.70272801,12.37591082\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.84423378,7.61242001,8.377270591,9.134283411,9.878904946,10.6067023,11.3136347\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,6.649230618,7.455257603,8.25592389,9.045352997,9.818427213,10.57063508,11.29813372\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.908296513,8.688761299,9.456123831,10.20757194,10.93982365,11.64953967,12.33370072\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,10.20095932,11.00349408,11.74297691,12.42893213,13.06899899,13.66905664,14.23353314\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,7.838556396,8.626104134,9.398042786,10.1523524,10.88637707,11.59723457,12.28221799\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.43245902,13.75890778,14.92201515,15.93666465,16.82016484,17.58968802,18.26105896\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,14.12025116,15.02926328,15.82994404,16.5398952,17.17306045,17.74054215,18.25127503\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.21150164,14.19026767,15.06311056,15.84339991,16.54276115,17.17118402,17.73722688\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.69571342,13.67732261,14.56122327,15.35764259,16.07607356,16.72508278,17.3122871\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,14.58977731,15.5473755,16.39153535,17.13800491,17.79984289,18.38803454,18.91193668\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.78722548,14.71526252,15.54131363,16.27906347,16.94008813,17.53413407,18.06942713\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.447652,14.30713651,15.09562658,15.8171158,16.47618847,17.07764815,17.62627504\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.56551969,13.56836281,14.47148954,15.28501339,16.01843893,16.6804288,17.27874947\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.88773667,13.80027249,14.63006458,15.38527977,16.07307157,16.69980312,17.27119555\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.8062978,13.56283881,14.24301536,14.85985132,15.42310782,15.94028418,16.41727871\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,11.84920584,13.20020245,14.39702857,15.44971256,16.37240581,17.18033677,17.88820752\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.88510852,14.74994564,15.5246567,16.22073803,16.84799233,17.41476144,17.92815879\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.21561148,13.96776194,14.64048655,15.24787359,15.8005173,16.30651778,16.77217499\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.51096448,14.39007092,15.18301508,15.9004835,16.55123139,17.14257669,17.68075732\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.6706644,14.56256316,15.36754923,16.09429908,16.75100226,17.34513012,17.88337765\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.5985611,14.5319817,15.36436412,16.10882701,16.77664546,17.37741501,17.91928846\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.55126343,13.51720158,14.39002807,15.18005596,15.89618921,16.54616918,17.13678565\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.50221606,14.46992943,15.32327332,16.08008755,16.75480552,17.35909744,17.90246114\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,14.39980261,15.20168354,15.91997041,16.56596771,17.14904135,17.67700879,18.15644811\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,14.02126017,14.9394468,15.74946361,16.46846767,17.11012714,17.68539547,18.20314731\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.89955563,13.81888511,14.65419268,15.4135989,16.10437641,16.73307067,17.30559536\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.7834603,13.74092005,14.6064635,15.38946418,16.09839649,16.74087413,17.32371689\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,14.92216119,15.85815256,16.67612324,17.39413601,18.02686144,18.58640478,19.08287914\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.15469855,14.11635955,14.97828793,15.7520017,16.44783365,17.07487251,17.64104334\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.77604838,14.71315685,15.54495528,16.28629717,16.94951215,17.54483231,18.0807981\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.08257278,14.06430593,14.93973773,15.72238189,16.42402188,17.05477237,17.62327072\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.67415891,14.567144,15.36078653,16.06965419,16.70564613,17.27853867,17.79642818\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,12.79742783,13.7324634,14.5821623,15.35428391,16.05600854,16.6939573,17.27420684\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.54686409,14.42578867,15.22147664,15.942645,16.59699392,17.19134289,17.7317507\n\"linker [O-]C(=O)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology rna\",,,13.68645517,14.59367883,15.40324413,16.12782262,16.77828332,17.36388744,17.89252318\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.97636688,16.04064763,16.94775528,17.7218133,18.3841298,18.95290418,19.44339262\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.99120217,16.05389191,16.95956809,17.73236173,18.3935717,18.96138154,19.45102997\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.91300328,15.98357921,16.89679969,17.6764229,18.34365557,18.91671284,19.41091236\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.89602202,15.96816959,16.88275147,17.66358071,18.33189286,18.9059206,19.40099403\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.866285643,4.464886389,5.092278802,5.731956248,6.370179248,6.996517773,7.603722449\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.838963644,4.439170141,5.068396514,5.710009128,6.350177874,6.978413911,7.587433621\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,9.323797043,9.829933341,10.32268923,10.79509403,11.24210865,11.66073059,12.04967896\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.870690992,4.469051213,5.096314901,5.735925489,6.37410923,7.000414882,7.60758133\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.843523975,4.44347477,5.072513783,5.713969815,6.353991372,6.982079396,7.590946789\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,9.352353859,9.851833092,10.33939063,10.8077367,11.25158353,11.66773384,12.05475416\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.86629288,4.464910457,5.092319198,5.732011663,6.370247867,6.99659754,7.603811263\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.839001409,4.439231009,5.068479249,5.710111513,6.350297125,6.978547031,7.587577666\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,9.323254523,9.829483701,10.32231254,10.79477532,11.24183651,11.66049621,12.04947549\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.870746601,4.469123893,5.096402958,5.736026704,6.37422116,7.000535088,7.607707529\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,3.843538535,4.443502125,5.072553737,5.714021426,6.354053238,6.982149906,7.5910243\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,9.352735422,9.852181998,10.33971249,10.80803529,11.25186151,11.6679932,12.05499653\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.58730177,7.336568617,8.082080855,8.819358981,9.544315716,10.2531126,10.9422511\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26100539,10.93405758,11.58852895,12.22208262,12.83239108,13.41755401,13.97623796\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26249508,10.93577194,11.59009773,12.2233285,12.8332528,13.41803387,13.97636902\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.54581612,7.298160215,8.046151286,8.78549764,9.512238119,10.22261925,10.91319932\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.601323953,7.34742963,8.090445505,8.825699504,9.548987406,10.25639639,10.94437725\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26757937,10.93926699,11.59268882,12.22544051,12.83513519,13.41982509,13.9781407\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26490786,10.93822107,11.59269269,12.22609041,12.83615548,13.42103118,13.97941104\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.588785249,7.332622873,8.07397277,8.808085837,9.530676992,10.23775438,10.92569543\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.587314401,7.336591752,8.082110233,8.819390773,9.544346806,10.25314066,10.94227457\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26112673,10.93418999,11.58867008,12.22223006,12.83254251,13.41770734,13.97639142\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26257185,10.93586349,11.59020048,12.22343924,12.83336877,13.41815274,13.9764889\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.545805477,7.298151736,8.046146403,8.785497185,9.512242445,10.22262836,10.91321297\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.60131857,7.347437757,8.090463709,8.825724979,9.549017872,10.25643003,10.94441264\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26763969,10.93933966,11.59277104,12.22552974,12.83522919,13.41992198,13.97823891\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,10.26495878,10.93827383,11.59274651,12.2261446,12.83620941,13.42108432,13.97946295\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,6.588812847,7.332645265,8.073990774,8.808100058,9.530687901,10.23776237,10.92570085\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.5022951,14.35417568,15.12007694,15.81098388,16.43601371,17.00282722,17.51793288\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.22192243,15.01564134,15.72940616,16.3729913,16.95488418,17.4823564,17.96161397\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.87585156,14.70689341,15.45237823,16.1231787,16.72860663,17.27656812,17.77376782\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.3111403,14.17641058,14.95518411,15.65824877,16.29462074,16.87192566,17.39667958\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.81020678,15.82905165,16.70650259,17.46284574,18.11620249,18.68227008,19.17440664\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.90073691,14.71123622,15.4417131,16.10209133,16.70063251,17.24431415,17.73909881\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.08033931,14.87953295,15.60013829,16.2511261,16.84050482,17.3752708,17.86148049\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.9179653,14.74384199,15.48596723,16.15445318,16.75816047,17.30473353,17.80072879\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.8576303,14.66872527,15.40105511,16.06392495,16.66521439,17.21167401,17.70913805\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.41739594,15.48780987,16.40818319,17.20038618,17.88386948,18.47540732,18.98921834\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.50195049,14.35385963,15.11978494,15.81071251,16.43576032,17.00258977,17.51770976\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.22174875,15.01547341,15.72923914,16.37282265,16.95471286,17.48218236,17.9614377\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.87633609,14.7072905,15.45270684,16.12345311,16.72883769,17.2767642,17.77393545\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.31082317,14.17611972,14.95491745,15.65800425,16.2943964,16.87171965,17.3964902\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.81244597,15.83099658,16.70820378,17.46434376,18.11752995,18.68345333,19.17546708\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.90051633,14.71105503,15.441562,16.10196359,16.70052322,17.24421967,17.73901638\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.07838129,14.87780568,15.59860114,16.24974764,16.83926037,17.37414076,17.86044907\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.91820914,14.74407113,15.48618204,16.15465424,16.75834849,17.30490929,17.80089307\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,13.85730357,14.66843105,15.40078867,16.06368234,16.66499233,17.21146983,17.70894954\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Al], [OH], topology pts,\",,,14.41823445,15.48855196,16.40884139,17.20097192,17.88439278,18.47587677,18.98964123\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,20.61457116,20.88622753,21.10014774,21.27144922,21.41066477,21.52529329,21.62077964\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,20.72552693,21.00300192,21.22173657,21.39704283,21.5396109,21.65706489,21.75494876\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,21.0093742,21.27885786,21.49097081,21.66076331,21.79871205,21.91227047,22.00684714\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,21.07813913,21.3522755,21.56829866,21.7413721,21.88208035,21.99796994,22.09452646\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.177757951,3.787324265,4.424385061,5.073628618,5.722275165,6.360507073,6.981359956\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.549711548,4.203364372,4.878360921,5.558039768,6.229235628,6.882406377,7.511260381\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.585518831,4.245650926,4.924002366,5.604435693,6.274463483,6.925183226,7.550824959\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.74379846,4.399999307,5.072204742,5.745124505,6.406921356,7.049156194,7.666369186\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.792099839,4.45241858,5.128932906,5.806055723,6.4716596,7.117089141,7.73675806\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.045438069,3.646433844,4.277654044,4.923610925,5.571128357,6.209909326,6.832512452\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.214442999,3.825429128,4.463349101,5.112972801,5.761600736,6.399491277,7.01974915\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.595311041,4.251104672,4.927008972,5.60660378,6.276966582,6.928769896,7.555898465\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.643945763,4.303832342,4.980316647,5.657789023,6.324205962,6.971001921,7.592644459\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.712721028,4.368516489,5.040561349,5.713579438,6.375732406,7.018571837,7.636624288\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.754359904,4.41122338,5.084744977,5.759482264,6.423367669,7.067747705,7.687001857\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.074724448,3.679517489,4.314360798,4.963544832,5.613754325,6.254630595,6.878730027\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.265437609,3.876826097,4.514556644,5.16349102,5.810994427,6.447369262,7.065750387\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.645041367,4.301622429,4.977739846,5.657060045,6.326733782,6.977489805,7.603254126\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.654767474,4.312695408,4.987681761,5.6640676,6.329733094,6.976031763,7.597356776\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.787087627,4.443320055,5.114629961,5.786021739,6.445908692,7.086043463,7.701102648\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.84670171,4.506492777,5.181510528,5.856513118,6.519646928,7.162456161,7.779490747\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.089902687,3.694029864,4.32816067,4.976640784,5.626186836,6.26645547,6.890007842\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.194293905,3.803244503,4.439582994,5.088067017,5.735956417,6.373455054,6.993609354\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.615284454,4.274883847,4.953481189,5.634698616,6.305703257,6.957276709,7.583415357\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.654222661,4.315299804,4.992945534,5.671433415,6.338637188,6.985944698,7.607806845\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.829787449,4.489097683,5.16226454,5.834469149,6.494309909,7.133708696,7.74748633\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.82208348,4.484453158,5.162353197,5.84027565,6.506183361,7.151511151,7.770756105\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,3.066975815,3.671747382,4.306436849,4.955426695,5.605464537,6.246228214,6.870290646\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.002894283,9.785808722,10.54604766,11.27987784,11.98430189,12.65709789,13.29682019\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.27828334,8.992630018,9.703288798,10.407821,11.10203014,11.7811693,12.44075139\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.758130581,10.52874352,11.26882837,11.97680521,12.65160032,13.29258513,13.89956137\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.709415267,10.50424693,11.2635835,11.98662255,12.67307609,13.32300843,13.93679378\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.586016385,8.392182787,9.192138759,9.980069655,10.75002707,11.49660258,12.2153423\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.539578007,8.348211402,9.150865637,9.941541778,10.7142137,11.46344511,12.18477401\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.775917599,10.56495614,11.32063402,12.04159158,12.72705709,13.37670872,13.99063045\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.864922687,10.63449204,11.3738563,12.08124725,12.75546201,13.39579116,14.00199199\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.304678437,9.025155251,9.7401937,10.44769693,11.14385313,11.82426558,12.48472964\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.981125037,9.770701813,10.53559155,11.27312474,11.980887,12.65694766,13.2999837\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.849149344,7.606090209,8.369336161,9.130616921,9.882592751,10.61887856,11.33414824\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.849938139,7.610917867,8.376885496,9.139852839,9.892791712,10.62960201,11.34518778\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.053608322,9.838121019,10.59955361,11.33425363,12.03929084,12.71249985,13.35248178\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.363039067,9.074215826,9.781362345,10.4823342,11.1731237,11.84909358,12.50581057\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.773708667,10.54372235,11.2825591,11.98876383,12.6614193,13.30004526,13.90456648\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.699455175,10.49164904,11.2482135,11.96839826,12.65199839,13.29915836,13.91031521\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.635513919,8.437755173,9.233534595,10.01730943,10.78330132,11.52620015,12.24160057\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.586718827,8.395204878,9.196620354,9.985390516,10.75580008,11.50262898,12.22155836\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.770568818,10.56497451,11.32470797,12.04870368,12.73641573,13.38769635,14.00276495\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.826187552,10.60044593,11.34354725,12.05394744,12.73059534,13.37289069,13.98067406\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.239555766,8.966106694,9.68689183,10.39959314,11.10029454,11.78457107,12.44823763\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.014050458,9.801145581,10.56327701,11.29797384,12.00293584,12.6762948,13.31675908\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.925165764,7.688573192,8.457379238,9.223466654,9.979564961,10.71932805,11.43746491\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.822589559,7.576278357,8.337453872,9.097430593,9.848617783,10.58447999,11.29959871\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.109457264,9.891371158,10.65083926,11.38407845,12.08803183,12.76042579,13.39977535\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.40951007,9.121840015,9.830657837,10.53351537,11.22619363,11.90392191,12.56219271\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.880794024,10.64719542,11.38306877,12.08685831,12.75755333,13.39459305,13.99783462\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.788781225,10.5781938,11.33263921,12.05127256,12.73379174,13.38025446,13.99102403\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.669449205,8.468582584,9.26181078,10.04356798,10.80803356,11.54984221,12.26452742\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.614932552,8.419464968,9.217377267,10.00310411,10.77091818,11.51557212,12.23271005\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.851065674,10.63676449,11.38916163,12.10697139,12.78948959,13.43644193,14.04793803\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.944169238,10.71128353,11.44812727,12.15301059,12.82480366,13.46285227,14.06694889\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.336997641,9.057534033,9.772489439,10.47978309,11.17563411,11.85567644,12.51573058\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.047609694,9.836071149,10.60034004,11.33758119,12.04520682,12.7211425,13.36396302\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.967889465,7.721687478,8.482779192,9.242591316,9.993551194,10.72909784,11.44377746\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.923249947,7.682672984,8.446984433,9.208316351,9.959702531,10.69506953,11.40932803\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.96606269,9.746387161,10.50407983,11.23551817,11.93777071,12.60864846,13.24671513\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.086832907,8.79751541,9.50418539,10.20469504,10.8950695,11.57071016,12.22721385\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.464942741,10.23303919,10.97069561,11.67636044,12.34899826,12.98801242,13.59322366\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.535458237,10.32619697,11.08198437,11.80192608,12.48568147,13.13327907,13.74506257\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.554740608,8.359733462,9.158267476,9.944667058,10.71308848,11.45819654,12.17558383\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,7.563925259,8.373457988,9.176216424,9.966480231,10.73841303,11.48670614,12.20698302\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.795718721,10.58629896,11.34317082,12.06493653,12.7508445,13.40061792,14.01439317\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,9.891041789,10.66188744,11.40183485,12.10933754,12.78335766,13.42330249,14.02900902\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.327023402,9.052842096,9.772483345,10.48387197,11.18322826,11.86619918,12.52863402\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,8.993826197,9.786910153,10.55487122,11.29508972,12.00516631,12.68317716,13.32780986\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.638075531,7.392613188,8.155510582,8.917804042,9.671614535,10.41015506,11.12781455\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,6.931172075,7.691094202,8.457678804,9.222356728,9.977595507,10.71689782,11.43488205\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.3535319,11.2222767,12.04649374,12.8256442,13.55965412,14.24891102,14.89426021\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.30687515,11.20377063,12.05108053,12.84903417,13.59826131,14.29976501,14.95491548\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.38673793,11.26245521,12.09179074,12.87452503,13.61089498,14.30156399,14.94760864\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.31677853,11.20597187,12.04701892,12.84007797,13.58562013,14.28446247,14.93779271\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.46880967,11.33693563,12.1591758,12.93551975,13.66628615,14.35213951,14.99411038\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.37433163,11.26783183,12.11210988,12.90741372,13.65432819,14.35379174,15.00711203\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.40860748,11.27410802,12.09472079,12.87015906,13.60051607,14.28628528,14.92837386\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,10.29423032,11.19622386,12.04754374,12.84872321,13.60059226,14.30428877,14.96127672\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.22079667,15.93224811,16.57691542,17.16184906,17.69312735,18.17607663,18.61542585\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.007265,15.7728465,16.46261227,17.08577597,17.65001244,18.16182339,18.62679894\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,14.43831481,15.27121518,16.02073641,16.69644738,17.30664661,17.85855076,18.35846424\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.2528261,15.97214579,16.62049774,17.20691243,17.73869287,18.2219015,18.66168407\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.21060898,15.98137592,16.67384756,17.29774846,17.86108453,18.37061371,18.83215246\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,14.89287971,15.67648114,16.38093162,17.01609503,17.59016511,18.11005855,18.5816975\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,14.93797085,15.70367714,16.39444124,17.01865399,17.58360245,18.09563735,18.56032364\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.20289754,15.94415065,16.61083625,17.21256737,17.75711087,18.25091779,18.69946701\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.59132922,16.30445709,16.95036498,17.53619571,18.0680893,18.55142161,18.99096454\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.15850881,15.890792,16.55494883,17.15783884,17.70560667,18.20373677,18.65712786\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.33324998,16.07339668,16.74046508,17.34329779,17.88927307,18.38464004,18.83476991\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,14.90832526,15.70211949,16.41253302,17.0511321,17.62712991,18.14805683,18.62020632\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.07892421,15.79824294,16.4510653,17.04373906,17.58201198,18.07109322,18.51571116\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.12429017,15.84443615,16.49726091,17.08968437,17.62782898,18.11712332,18.56240027\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.02439149,15.80472352,16.50796936,17.14274874,17.71657413,18.23601201,18.70682882\n\"linker [O-]C(=O)c1ccc(nc1)c1ccc(cn1)C(=O)[O-], nodes [In], topology utp,\",,,15.35234399,16.09215749,16.75794069,17.35918218,17.90354414,18.39739272,18.84614032\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,20.89531295,21.36102409,21.73646777,22.04289934,22.29580358,22.50664943,22.68405653\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,21.26791034,21.70916793,22.05793674,22.33786963,22.56565461,22.75329446,22.90957614\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,21.1439274,21.57288072,21.91872297,22.20108082,22.43421111,22.62865741,22.79233855\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,21.61695674,22.00290323,22.30823686,22.5535164,22.75325738,22.9179096,23.05513043\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,20.88951998,21.35695573,21.73350733,22.04067542,22.29408523,22.50528856,22.68295539\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,21.31106536,21.74408455,22.08669492,22.36193077,22.58606597,22.77082105,22.92478713\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,21.01298138,21.46222019,21.82421128,22.11956811,22.36327847,22.56642827,22.73734144\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,21.36430878,21.79004373,22.12669379,22.39700245,22.61702699,22.7983239,22.94935823\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.574674384,4.260240084,4.963107015,5.665880248,6.355325209,7.022218309,7.660775871\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.378006699,4.053797873,4.751452918,5.452679847,6.143417222,6.813716209,7.457181097\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.543531525,4.220086977,4.912848234,5.605392177,6.285241149,6.94366005,7.575115461\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.701417014,3.113619641,3.570209536,4.064025557,4.585683479,5.125458635,5.674462017\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.667162515,3.080262058,3.53682555,4.030091195,4.550997253,5.090051116,5.638514208\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.519537112,4.198915234,4.895582679,5.59257416,6.27698034,6.939765703,7.575213146\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.327570558,4.000971285,4.698238836,5.40062665,6.093616062,6.766874747,7.413717076\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.602484507,4.2908025,4.994796333,5.697409585,6.385778828,7.051007493,7.687568857\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.583809388,4.270832891,4.974928426,5.678670412,6.368823718,7.036184204,7.674998307\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.380166503,4.056878831,4.755281346,5.457091368,6.148263913,6.818870113,7.462534932\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.543002659,4.219692913,4.912466638,5.604923637,6.284601374,6.942770786,7.573897143\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.668630049,3.087385011,3.549307906,4.047402085,4.57244636,5.114862684,5.665887078\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.65792664,3.074404443,3.533877352,4.029587273,4.552491558,5.093128629,5.642797848\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.514570696,4.193491736,4.889753695,5.586400682,6.270530704,6.933111018,7.56842276\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.324407388,3.997323955,4.694291452,5.396514087,6.089435983,6.762697156,7.409591545\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.607845433,4.297327019,5.002266928,5.705605308,6.394493489,7.060059697,7.696805796\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.584876596,4.27119165,4.97465506,5.677861348,6.367579023,7.034597911,7.673153652\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.380468418,4.056247696,4.753900932,5.455125291,6.145852594,6.816130783,7.459563391\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.542517468,4.219417136,4.912507416,5.605353782,6.285470175,6.944118116,7.57576491\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.68329065,3.099394973,3.558950902,4.054982879,4.578274193,5.119241203,5.669107856\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.672537657,3.085319677,3.541629418,4.03468243,4.555397649,5.094270988,5.64255898\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.524136554,4.203456332,4.899840603,5.596408929,6.280319975,6.942587931,7.577529153\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.330817737,4.004027647,4.701082428,5.403251144,6.096024651,6.7690765,7.415724566\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.608741088,4.297794498,5.002276695,5.705162544,6.393628706,7.058818922,7.695242452\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.577013758,4.262698054,4.965734102,5.66868606,6.358292657,7.025315945,7.663966714\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.388127966,4.06435167,4.762330913,5.463762091,6.154585678,6.824863728,7.468216079\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.539638817,4.215956691,4.908625284,5.601180798,6.281112687,6.939661375,7.571276041\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.68313139,3.099059094,3.558543762,4.054570618,4.577886898,5.118876577,5.668736174\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,2.666615642,3.079589478,3.535967719,4.02901556,4.5496835,5.088482302,5.636671576\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.51832178,4.197352641,4.893759873,5.590550165,6.274800153,6.937466771,7.57282799\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.33602963,4.010832306,4.709125807,5.412176485,6.105515999,6.778874132,7.425625423\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,3.596575324,4.285234361,4.989519991,5.692389762,6.380991466,7.046436687,7.683204074\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.793504573,8.597618985,9.382186591,10.14628189,10.88809231,11.60531531,12.29562147\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.512143617,10.27638935,11.02067136,11.74053258,12.43222407,13.09297848,13.72103009\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.895922276,8.683016306,9.4550435,10.20954851,10.94365367,11.65438753,12.33903003\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.41789562,10.19536518,10.95246126,11.68400748,12.38600019,13.05565086,13.69128265\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.909926808,8.699309808,9.474380866,10.23221025,10.96959129,11.68334217,12.37062251\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.611694517,10.38399686,11.13592749,11.8626583,12.56016167,13.22551709,13.85691848\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.725248187,7.505687488,8.283910871,9.053830871,9.810116618,10.54805475,11.26360452\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.778282863,7.558864245,8.33547041,9.102764587,9.855946624,10.59064835,11.30303607\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.482522522,10.331855,11.15922724,11.95595194,12.71518184,13.43239138,14.10524053\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.801288407,8.605994507,9.390573391,10.15430279,10.89550106,11.6119595,12.30141936\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.609069145,10.37664025,11.12436682,11.84750843,12.54206112,13.20508121,13.83471036\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.892645521,8.683581662,9.461226244,10.22209604,10.96259663,11.67930342,12.36924307\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.437189987,10.21781789,10.97709243,11.71019023,12.41329851,13.08373284,13.71987753\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.875602183,8.668413624,9.445873545,10.20543149,10.94414156,11.65898923,12.34723592\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.543700988,10.30791821,11.05205714,11.77153161,12.46256977,13.12243729,13.74942379\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.987917731,7.740883438,8.491488576,9.234765397,9.966074302,10.68109006,11.37594522\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.683772771,7.481388063,8.273419,9.054253994,9.819038412,10.56349362,11.28395612\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.762155789,8.571273069,9.359363799,10.12598396,10.86964222,11.58825397,12.27963837\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.516197485,10.28224729,11.02778475,11.74847303,12.44066081,13.10166044,13.72977055\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.893860617,8.683090826,9.456731833,10.21243595,10.94741467,11.6587686,12.343835\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.398013436,10.17811831,10.9374265,11.67085497,12.37446147,13.04550154,13.68233228\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.890497507,8.680827516,9.456533953,10.21477829,10.95243403,11.66638353,12.35383361\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.593942062,10.36806772,11.12138054,11.84915376,12.54744594,13.21340629,13.84528235\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.716555917,7.50300823,8.285812311,9.059115995,9.817818731,10.5574136,11.27403496\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.777154815,7.557327305,8.333220075,9.099708955,9.852114365,10.58613066,11.29795075\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.399149121,10.27131736,11.11557672,11.92479511,12.69327774,13.41734637,14.09528149\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.803776056,8.613427152,9.401861733,10.16853276,10.91191653,11.62994272,12.3204711\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.610038829,10.37779691,11.12555763,11.84862513,12.54303536,13.20587608,13.83531171\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.901438222,8.690464432,9.466396763,10.22572776,10.96485227,11.6803403,12.36921357\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.454033813,10.23311728,10.99103554,11.72290908,12.42489874,13.09430782,13.72951434\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.885543215,8.67700061,9.453561814,10.21253352,10.95085972,11.66544753,12.35350559\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.544614192,10.31045909,11.05595965,11.77655981,12.46851183,13.12910427,13.75664929\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.020713791,7.769298164,8.516436335,9.257223884,9.986915931,10.70101312,11.39546311\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.755018463,7.538519316,8.319491009,9.091610723,9.849503143,10.58849463,11.3046156\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.769246308,8.579048748,9.367810437,10.13505347,10.87925823,11.59832197,12.29005587\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.524511715,10.28928684,11.03379665,11.75366414,12.44519879,13.10567827,13.73337217\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.911805834,8.698020426,9.469041032,10.22249372,10.95555366,11.66528237,12.34897905\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.440100154,10.21564422,10.97093645,11.70082209,12.40130117,13.06958061,13.70397515\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.917079082,8.706882919,9.481878844,10.23932372,10.97614353,11.68924787,12.37585719\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.613474143,10.38767149,11.14082422,11.86830784,12.56623501,13.23178391,13.86321875\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.752811294,7.530464129,8.30656714,9.074785946,9.829643201,10.56633811,11.28077727\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.750793617,7.537162032,8.318173451,9.088752429,9.844343747,10.58079085,11.29443277\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.4467257,10.31091286,11.14875321,11.95280534,12.71711709,13.43780427,14.11298573\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.812317057,8.620847662,9.408160861,10.17374729,10.91611263,11.63320588,12.32289705\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.601027465,10.37070296,11.11994356,11.84417347,12.53950671,13.20308533,13.83311345\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.893593377,8.685899721,9.464400607,10.22576172,10.96649672,11.68326042,12.37313773\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.461738785,10.24275239,11.00200078,11.73477718,12.43735475,13.10711358,13.74248675\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.883134273,8.677205454,9.455919696,10.21665023,10.9563966,11.67211332,12.36105046\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.547694097,10.31246977,11.0569431,11.77658703,12.46767391,13.12750343,13.7543913\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.97402789,7.734651185,8.49101182,9.238773001,9.973683055,10.69165108,11.38895159\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.702251578,7.498599013,8.289635541,9.069646221,9.833716681,10.5775326,11.29740844\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.801795793,8.607483937,9.39260447,10.15664604,10.89805398,11.61468725,12.30431721\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.525662091,10.28888956,11.03217706,11.75107703,12.4418486,13.10173224,13.72896869\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.879568839,8.668582501,9.442289937,10.19826409,10.93365326,11.6455092,12.33113236\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.437849773,10.21501881,10.97185194,11.70314591,12.40487247,13.07422659,13.70952312\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.909723689,8.700259668,9.476420288,10.23523745,10.97348289,11.68796649,12.37584917\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.625717638,10.39759261,11.14904675,11.87526277,12.57222614,13.2370292,13.86787701\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.711938085,7.498446387,8.281395202,9.054948098,9.813987644,10.55397902,11.27102846\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.781788652,7.56088618,8.336788618,9.10382979,9.857007166,10.59183074,11.30439495\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.452781481,10.31269758,11.14763341,11.94974452,12.71278933,13.43267712,14.10737996\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.811022306,8.618027153,9.404539683,10.16981887,10.91219828,11.62950358,12.31951898\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.640402099,10.40688891,11.1536181,11.87578845,12.56936984,13.23141094,13.860055\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.9091802,8.698391759,9.474694237,10.23445768,10.97400561,11.68986794,12.37904587\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.461802919,10.24168193,11.00014009,11.73231729,12.43441409,13.1037773,13.73882458\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.876609142,8.668510472,9.445408134,10.20462031,10.94311885,11.65783856,12.34600994\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,9.517506092,10.28436382,11.03072063,11.75206766,12.44470022,13.10593953,13.73411957\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,7.048027274,7.789038567,8.530635464,9.267250888,9.993734274,10.70532864,11.3978104\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,6.768860886,7.548334717,8.326995558,9.097892161,9.855234973,10.59407803,11.31027442\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,15.07148019,15.85013454,16.54180512,17.16029194,17.71641234,18.2187449,18.67419001\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.08541382,14.94871411,15.73099264,16.43911495,17.07997275,17.66014887,18.18575259\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.83448407,15.63582766,16.34818972,16.98537899,17.55831128,18.07570216,18.54460297\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.74736457,14.64527296,15.4577328,16.19220376,16.85610165,17.45647081,17.99982282\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.21165113,14.07044688,14.86603184,15.60052214,16.27652751,16.8971204,17.46572295\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,12.61354555,13.55220758,14.41333935,15.20220658,15.92377337,16.58288279,17.18430488\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,15.09977185,15.84892026,16.51608236,17.11479272,17.65533149,18.145671,18.59212771\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.02466893,14.89819714,15.68511304,16.39504388,17.0364208,17.61664903,18.14225291\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.32982861,15.17774707,15.93174457,16.60582828,17.21134149,17.7575022,18.25185828\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.48216732,14.39392475,15.2216363,15.9718487,16.65132565,17.26668886,17.82420128\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,15.18075948,15.95130997,16.63399272,17.24347388,17.79102998,18.28546087,18.73375087\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.31230343,14.24243098,15.08657675,15.85124881,16.5433458,17.16968828,17.73674965\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.70156439,15.52996421,16.26326992,16.91684535,17.50272219,18.03042574,18.5076032\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.64992498,14.56064392,15.38324021,16.12590197,16.79654482,17.40256226,17.95071425\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,11.94625296,12.93316429,13.83971555,14.67087097,15.43151513,16.12655429,16.76090589\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,11.98603528,12.97460463,13.88189313,14.71312313,15.47336501,16.16765893,16.80102087\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.69751204,15.49427713,16.20271191,16.83724117,17.40891186,17.92634878,18.39642426\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.49468917,15.33156454,16.08316654,16.76007942,17.37112072,17.92376146,18.42442195\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,15.47244764,16.18937055,16.83370626,17.41505822,17.94143313,18.41949016,18.85479258\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.75951601,14.64391128,15.44739824,16.17608408,16.83641494,17.43475044,17.9771212\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,15.05907566,15.8417594,16.53667912,17.15767952,17.71568346,18.21938896,18.67580765\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.28743752,15.12795636,15.89162421,16.58420863,17.21186114,17.78065256,18.29632791\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.31791446,15.17612783,15.93733975,16.61655268,17.22575517,17.77458316,18.27085935\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.7699935,14.667429,15.47856809,16.21125546,16.8731713,17.47153212,18.01295486\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,12.01436931,12.99692299,13.89926837,14.72643016,15.48332222,16.17486119,16.80596345\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,12.32248267,13.27584887,14.15248223,14.9570183,15.69396989,16.36788397,16.98335334\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.60950208,15.41852571,16.1375505,16.78117657,17.36063822,17.884738,18.36050847\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.8525456,14.74945894,15.55334705,16.27594854,16.92710849,17.51516947,18.04727314\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.70027357,15.50693397,16.22609659,16.87052341,17.45058603,17.97474304,18.4499452\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.2057569,14.14519377,14.99715544,15.76861495,16.46673582,17.09849766,17.67047558\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.88250676,15.68557734,16.39714287,17.03204543,17.60187341,18.11577968,18.58109617\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,13.86963832,14.75864591,15.5621634,16.28807022,16.94399507,17.53706723,18.07380822\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.70405165,15.51930237,16.24418333,16.89244564,17.47508366,18.00094779,18.47723899\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.28965726,15.13914619,15.90686106,16.60051484,17.22751571,17.79473196,18.3084049\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,12.4290638,13.37307962,14.24124522,15.0380869,15.76804775,16.43562212,17.04535551\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,12.47978265,13.42780778,14.29774052,15.09484275,15.82407326,16.49028015,17.09824993\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,15.69379946,16.36644989,16.97317572,17.52315012,18.02364709,18.48052477,18.89858726\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.52643991,15.35251888,16.09604819,16.7668371,17.37319443,17.92224321,18.42015541\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,15.41760248,16.1335875,16.77851425,17.36129679,17.889542,18.36967954,18.8071413\n\"linker [O-]C(=O)c1cc(OCOc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Zn], topology rna,bcu\",,,14.11685492,14.96141171,15.73249027,16.43421776,17.07169711,17.65035806,18.17557271\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,17.8297222,18.24603361,18.58115915,18.85412871,19.07892808,19.26595045,19.42300889\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,18.45209968,18.78684933,19.0540311,19.27016426,19.4471614,19.59373819,19.71636302\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,3.061535152,3.720528894,4.390172805,5.056390345,5.709232742,6.342212931,6.95154887\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,2.872137998,3.518817154,4.182068417,4.846681541,5.501626333,6.139487906,6.755734032\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,3.322888104,4.005058946,4.690230753,5.365341882,6.021600594,6.653631513,7.258634124\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,2.95770732,3.608486196,4.273329504,4.93766495,5.591067091,6.226641622,6.840274457\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,6.309496194,7.030564295,7.761576498,8.494887834,9.223379314,9.940582573,10.64088347\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,9.276473894,10.06026092,10.7959824,11.48627055,12.13421625,12.74292322,13.31527689\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,6.190100275,6.949034735,7.714332392,8.47791923,9.232469581,9.971556358,10.68980431\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,9.325868163,10.11153891,10.85009132,11.54415723,12.19657831,12.81013616,13.38741057\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,6.297281174,7.038772733,7.783821505,8.525599947,9.258081308,9.975907793,10.67445824\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,9.396000413,10.16874956,10.89443669,11.57628945,12.21742506,12.82073019,13.38880168\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,6.276846701,7.018693093,7.765529405,8.509935335,9.245437144,9.966367469,10.66790668\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,9.316337212,10.09548609,10.82903064,11.51950376,12.16956302,12.78177834,13.35852393\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,13.09554982,13.95808123,14.73676075,15.44032142,16.07665512,16.65283683,17.17518071\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,14.19617419,15.00800635,15.72816375,16.37081222,16.94701142,17.46557422,17.93367784\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,13.57617313,14.40915879,15.14913239,15.810434,16.4044551,16.94032606,17.42545807\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,12.93036101,13.8811242,14.73018072,15.48937293,16.16925952,16.77912884,17.32711689\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,13.05211402,13.92279266,14.70401395,15.40684624,16.04082412,16.61407438,17.13352985\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,14.18581269,14.97711563,15.67934676,16.3060414,16.86817564,17.37461683,17.83257102\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,14.01257573,14.78338234,15.47380538,16.095145,16.65657672,17.1655798,17.62831907\n\"linker [O-]C(=O)C=CC(=O)[O-], [O-]C(=O)[CH][CH]C(=O)[O-], nodes [Co], topology \",,,13.35839414,14.23535206,15.01700407,15.71578575,16.34248278,16.90625478,17.4148394\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,18.40107616,18.77234145,19.07040423,19.31279296,19.51223468,19.67810035,19.81738706\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,18.87625445,19.1946717,19.44640617,19.64852455,19.81305787,19.94865372,20.06164031\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,3.409408643,4.064534832,4.739574842,5.418572558,6.088926771,6.741482224,7.370173779\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,3.342361729,3.999064419,4.6762925,5.357892939,6.03112165,6.686723853,7.318567422\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.152740951,6.92460596,7.70059049,8.472567412,9.233506076,9.977390863,10.69924875\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.841744618,7.708537535,8.560411674,9.390685094,10.19391341,10.96582987,11.7033186\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.183810496,7.979519261,8.763546145,9.532445599,10.28210755,11.0084686,11.70799042\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.074439245,6.904764147,7.725233426,8.529794187,9.313669604,10.07293059,10.80438868\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,8.764907549,9.574362419,10.35110955,11.09302545,11.79884539,12.4679776,13.10038831\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.212535892,6.96970661,7.722912199,8.466586181,9.19628299,9.908218767,10.59914154\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.80618365,7.65895975,8.50033149,9.322975,10.12090284,10.88938936,11.62493343\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.169720014,7.960093609,8.737283298,9.49860344,10.24058879,10.95965548,11.65258088\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.070473738,6.909990015,7.742847922,8.5614813,9.359813256,10.13294223,10.87703833\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,8.723490611,9.544726169,10.33327924,11.08656951,11.80298932,12.4817197,13.12260437\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.50933178,15.26825065,15.941961,16.54458665,17.08680888,17.57689106,18.02139073\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.53553835,15.26860256,15.92577521,16.51788818,17.05356513,17.53975866,17.9821711\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.37134473,15.09479213,15.74111655,16.32345722,16.85144862,17.33234386,17.77177596\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,13.98656675,14.80813162,15.53682051,16.18688347,16.76978049,17.29471548,17.76914499\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.34266412,15.08548671,15.74529354,16.33573129,16.86747911,17.34891429,17.78667325\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,15.00914007,15.68161381,16.28247536,16.82360913,17.31395911,17.7603681,18.16818956\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.52821902,15.2398924,15.87360331,16.4429591,16.95804895,17.42649957,17.8542131\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.17680002,15.01742129,15.76445722,16.43100132,17.02776116,17.56357613,18.04584442\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,18.50669072,18.98970641,19.37884148,19.69610345,19.95765638,20.17550152,20.35865494\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,19.22188997,19.70196198,20.08701737,20.39973664,20.65666245,20.87000429,21.04888707\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,19.93415285,20.37930208,20.73412108,21.02086448,21.25551839,21.44974069,21.61216107\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,19.61201836,20.09462493,20.4820826,20.79702495,21.05598767,21.27118829,21.4517648\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,19.75586626,20.22998462,20.60950842,20.91724065,21.16975154,21.37922632,21.55474118\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,19.81723064,20.26448595,20.6208106,20.90865142,21.14412011,21.33895812,21.50185162\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,19.74763785,20.225914,20.6092491,20.92037609,21.17585678,21.3879017,21.56562765\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,18.66640171,19.15061492,19.540246,19.85756805,20.11891538,20.33639846,20.5191035\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,3.677808889,4.410623142,5.146815346,5.869936893,6.568634807,7.235779381,7.867536283\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,2.84482903,3.467423165,4.127227432,4.804738815,5.484249474,6.154081132,6.806200812\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,4.075758109,4.812474623,5.542058889,6.250742547,6.929297321,7.572055477,8.176029751\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,2.333101448,2.882391064,3.483864188,4.119795232,4.774550669,5.435506788,6.093127543\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,4.576067222,5.362634405,6.116281972,6.828331935,7.494232536,8.112359395,8.683086123\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,3.882451714,4.66627126,5.445305879,6.201821373,6.924462083,7.606865503,8.24634182\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,3.845649075,4.571570362,5.298109535,6.009857763,6.696262437,7.350751483,7.969845407\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,4.015029814,4.771935684,5.515316104,6.232421068,6.915035206,7.558412689,8.16036414\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,3.956332823,4.726877082,5.499936557,6.256939383,6.985424863,7.677920746,8.330750231\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,3.692575668,4.421632422,5.153791699,5.872913567,6.567819501,7.231458147,7.860011477\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,3.826734881,4.287625961,4.727073121,5.138996427,5.520585565,5.871248727,6.191791027\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,5.232613325,6.002492941,6.727134654,7.402412105,8.027038462,8.601696861,9.128366923\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,5.644947943,6.222007889,6.76564041,7.273061809,7.743099182,8.17597718,8.572950872\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,5.149774345,5.879164319,6.573511646,7.228284456,7.841067666,8.411125869,8.938995839\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,4.520814579,5.325031313,6.11625509,6.87877342,7.602914999,8.283630641,8.919217933\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,3.741561665,4.515092971,5.287250225,6.039772523,6.760737416,7.443261925,8.084215965\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.723253903,7.550521444,8.378111258,9.196551182,9.997852151,10.77551976,11.52454213\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,8.02613364,8.708160269,9.377933229,10.03187254,10.66621442,11.27759156,11.86333318\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.147058858,6.890643607,7.619175669,8.330520519,9.023629732,9.697617808,10.35146404\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.539728363,10.32586608,11.09409176,11.83828365,12.5532242,13.23506303,13.88136975\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.732397775,8.544447772,9.352347439,10.14851194,10.92568959,11.67769051,12.39970862\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.355510053,8.027537711,8.699252529,9.367431257,10.02814133,10.67724918,11.31084298\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.486094268,10.2343224,10.97403924,11.6976284,12.39835011,13.07094001,13.71173756\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.352759554,8.103913029,8.840161748,9.554790478,10.24258048,10.8997876,11.52400653\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.962668034,8.668657257,9.356038954,10.02297344,10.66711993,11.28619028,11.87828981\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.103576195,7.782076904,8.457139171,9.122579114,9.772746982,10.40283693,11.00905212\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,8.35703065,8.995657753,9.625862037,10.24454689,10.84856759,11.43501211,12.00139294\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.531506363,8.144111871,8.755712227,9.36600052,9.973321828,10.57504568,11.16804023\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.084350872,7.805142096,8.514677579,9.206387456,9.874996888,10.51655465,11.1283493\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.16775213,7.841834164,8.515589721,9.185921126,9.848946191,10.50052023,11.1366833\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.646133549,8.296597867,8.942103317,9.582501231,10.21620325,10.84066745,11.4529147\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,8.229948774,8.926142035,9.611386578,10.28032301,10.92833663,11.55180099,12.14811884\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.73776022,10.54500866,11.33234408,12.09182447,12.81753388,13.50558823,14.15388261\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.447278454,7.233162665,8.014253914,8.78443162,9.538741259,10.27299199,10.98366532\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.248977273,7.036223188,7.821781603,8.598510961,9.360556817,10.10301248,10.82183545\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.84543209,10.66967079,11.47198623,12.2438475,12.9791566,13.67413295,14.3269425\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.188453967,6.939436515,7.677774305,8.400416336,9.105469554,9.791356485,10.45654172\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.291954351,7.92303221,8.551923045,9.173261086,9.782254161,10.37479275,10.94752865\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.802087009,7.559790046,8.29696556,9.012147729,9.705074264,10.37567617,11.02370769\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.862063194,8.541377758,9.211638168,9.867417407,10.50403053,11.11776152,11.70590177\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,8.101502902,8.80051858,9.489081353,10.1624096,10.81612494,11.44657503,12.05097504\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,8.261544389,8.974109839,9.674526621,10.35769175,11.01917466,11.65544773,12.26394758\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.684008877,8.338828364,8.989768598,9.636203054,10.27615125,10.90677159,11.52487159\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.641795626,7.470645844,8.30255898,9.127148884,9.935642184,10.72091917,11.47750431\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.669998963,8.281981808,8.89061732,9.496342785,10.09813844,10.69389163,11.28086908\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,6.86999014,7.631107059,8.372832959,9.093446936,9.792368272,10.46921089,11.12345293\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.665891006,8.493563832,9.316140168,10.12582281,10.91521611,11.67806013,12.40954619\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.307746569,8.01536687,8.714855196,9.400560601,10.06737556,10.71099612,11.32807635\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.682807442,10.44120719,11.17816317,11.8908473,12.57619755,13.23154485,13.85491924\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.881100511,10.75703493,11.61515957,12.4446473,13.23701558,13.98650563,14.68987536\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.443491328,8.186981919,8.923821478,9.647760321,10.35260504,11.03296184,11.68462106\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.01488856,9.737823572,10.44209372,11.12630847,11.78806323,12.42479324,13.03427816\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.599003507,8.337818732,9.069225541,9.786845566,10.48454316,11.15711926,11.80062377\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,10.24675937,11.18683274,12.0793428,12.92068815,13.70887431,14.44344896,15.12524013\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.123288469,9.861426094,10.59168589,11.30841772,12.00576163,12.67854847,13.32274001\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.443257657,10.15141717,10.84108709,11.51095985,12.15887485,12.78253237,13.3799297\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.713364087,10.46600691,11.19727535,11.90469783,12.58542531,13.23688872,13.85713772\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.878115081,10.62379839,11.35167257,12.0596974,12.7447721,13.40371405,14.03382705\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.464299775,8.205407721,8.939769398,9.660568647,10.36138468,11.03684739,11.68291635\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.921888214,10.81814278,11.67956007,12.50137863,13.27977576,14.01232148,14.69800033\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.978475832,8.722288491,9.455210777,10.17265461,10.86958013,11.54140484,12.18448424\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,7.618690636,8.352750758,9.079591082,9.793586242,10.48897461,11.16062643,11.80446573\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.944825023,10.67995532,11.39666406,12.09358262,12.76809518,13.41733034,14.03876033\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,10.06017341,11.01421153,11.93575615,12.81374581,13.64092284,14.41343969,15.13014696\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,13.29886734,14.0912461,14.79535285,15.42432747,15.98916346,16.49892337,16.96103162\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,10.35822407,11.12302946,11.82529941,12.46908463,13.05883752,13.59899563,14.09379046\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,13.16281796,13.98465614,14.71723662,15.37323153,15.96320139,16.49587728,16.97847963\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,13.34921343,14.13917438,14.84059402,15.46672262,16.02862801,16.53542215,16.99456274\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,12.08533022,12.78829569,13.42989744,14.01547784,14.55042266,15.03974261,15.48793533\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.858513433,10.60018468,11.28137202,11.90621299,12.47915786,13.00456876,13.48654941\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.726280638,10.36951226,10.95261343,11.48307169,11.96755806,12.41175737,12.82040585\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,13.9734976,14.84477764,15.6151301,16.29949444,16.90994033,17.45633897,17.94687404\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,14.44740203,15.27593304,16.02190426,16.69443304,17.30138985,17.84967692,18.34541439\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,9.920776059,10.54780305,11.11541997,11.6315354,12.10298956,12.535497,12.93374808\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,14.53953169,15.36027501,16.0996663,16.76643172,17.36821879,17.91180188,18.40322525\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,13.57128003,14.28803762,14.93995163,15.53351421,16.074858,16.56948564,17.02222133\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,14.09253914,14.99232303,15.7885028,16.49596563,17.12705452,17.69200266,18.19933751\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,14.39461143,15.26078602,16.02316753,16.69866658,17.30063711,17.83970749,18.32443853\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,12.6691909,13.4778224,14.20024181,14.84835864,15.43224078,15.9602841,16.43946336\n\"linker [O-]C(=O)C1=CC=N[N]1, [O-]C(=O)C1=C[CH]N=N1, [O-]C(=O)C1=NN=C[CH]1, [O-]C(=O)[C]1C=CN=N1, nodes [Cu], topology pcu\",,,14.03058286,14.89607301,15.66029009,16.33884824,16.94420413,17.4864111,17.97369892\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,21.02597533,21.43366633,21.75626091,22.0154865,22.22666399,22.40081327,22.54600572\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,20.79116801,21.23290696,21.58307347,21.86482496,22.09457573,22.2841785,22.44234067\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,21.01262936,21.42102281,21.74447952,22.00459856,22.21664054,22.39159858,22.53753413\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,21.04819542,21.45225637,21.77203487,22.02903358,22.23842083,22.41111009,22.55509671\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,20.88588274,21.31324964,21.65196499,21.92447547,22.14667893,22.33004893,22.48301124\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,21.03633267,21.44117254,21.76178466,22.01960157,22.22975969,22.40315969,22.54779382\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.399911648,4.094243067,4.803921235,5.512041856,6.205889075,6.876657926,7.518854255\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.031503111,5.743642366,6.428553121,7.082451086,7.702988356,8.288842107,8.839518534\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.278414447,5.551621553,5.872117962,6.2330792,6.625790595,7.041304354,7.471441185\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.106479459,5.376079601,5.693492679,6.052207385,6.443714472,6.859155267,7.290342445\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.273087154,5.542091576,5.856402848,6.210126127,6.595285141,7.00344045,7.426713109\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.390538825,4.084012953,4.793247282,5.501266583,6.195288396,6.866456128,7.509239705\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.661353081,4.343589311,5.026255321,5.697546021,6.349045802,6.974958832,7.571524178\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.28930374,5.562172087,5.882595042,6.243672729,6.636628601,7.052467741,7.482978277\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.12727332,5.395048941,5.710921223,6.068385438,6.458906827,6.873589301,7.304207637\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.293020337,5.559823484,5.872708709,6.22563023,6.610444629,7.018560791,7.441977657\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.368324475,4.062717263,4.773901755,5.484479933,6.181328067,6.855344054,7.500838161\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.681281212,4.378858384,5.076891123,5.762816774,6.427893401,7.06641529,7.675062032\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.264541977,5.544397689,5.870514063,6.236164468,6.632736667,7.051384117,7.484024766\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.127913042,5.398180312,5.716268254,6.075603887,6.467623469,6.883430417,7.314817258\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.278219377,5.547779805,5.862960644,6.21779242,6.604191961,7.013617747,7.438110394\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.399104698,4.09343291,4.803114446,5.511245298,6.205108956,6.875899354,7.518121114\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.059925217,5.769999886,6.453000195,7.105142841,7.7240726,8.308455274,8.857784513\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.278429383,5.551274164,5.87149649,6.232262709,6.62484402,7.040278455,7.470374333\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.104503775,5.374458977,5.692108903,6.050982823,6.442598436,6.858115028,7.289357179\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.273211065,5.541981927,5.856084641,6.20963353,6.594653724,7.002703417,7.425899654\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.389950446,4.08340639,4.792600582,5.500573638,6.19455221,6.865684438,7.508442223\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.722579752,4.406471741,5.089878913,5.761114179,6.411905075,7.036597526,7.631558547\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.289023294,5.562665032,5.883791452,6.245483264,6.638953656,7.055207027,7.486037686\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.131472124,5.400052596,5.716660805,6.074740407,6.465736135,6.880752308,7.311576068\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.297989304,5.566714798,5.881302084,6.235635505,6.621551493,7.030472371,7.454429175\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.366259948,4.06067693,4.771848855,5.482407493,6.17924442,6.853263893,7.498777468\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,3.69159108,4.390093632,5.088676583,5.77484948,6.439943341,7.078315364,7.686695422\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.270064054,5.548730954,5.873944056,6.238903163,6.634942587,7.053176488,7.485493708\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.137023934,5.405494768,5.722230633,6.080535409,6.471759408,6.886945067,7.317841095\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,5.28170629,5.550865222,5.865688887,6.220195926,6.60629942,7.015456718,7.439707699\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,6.615203556,7.42435885,8.233556293,9.034683237,9.820761945,10.58591125,11.32538322\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.734605363,8.542034964,9.339004468,10.12095757,10.88297948,11.62049007,12.32967149\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.275000802,8.141628004,8.989449838,9.814411369,10.61267698,11.38081044,12.11600897\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,9.293200427,10.1217064,10.91468245,11.67038886,12.38784867,13.06669706,13.70709443\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.59338368,14.93463112,15.29453088,15.6649343,16.03802368,16.40724951,16.7676072\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,6.705270484,7.5272739,8.346514186,9.155235284,9.946771066,10.71552298,11.45700714\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.697314216,8.506769112,9.305580039,10.08917634,10.85267892,11.59155138,12.3020114\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.298069069,8.162613144,9.007929364,9.830215189,10.62581202,11.39140093,12.12425036\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,9.305348339,10.13180358,10.9230257,11.677195,12.39329559,13.07094519,13.71029531\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.52468812,14.87459707,15.24089316,15.61629442,15.99348874,16.36621975,16.72965383\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,6.679657806,7.491304987,8.301985271,9.103206023,9.88794339,10.65048602,11.38636117\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.733975007,8.545808116,9.347467391,10.1338895,10.89987757,11.6407256,12.35258992\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.338338263,8.202424665,9.046926646,9.868071325,10.66227574,11.42630345,12.15749593\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,9.320330865,10.14343915,10.93196309,11.68400801,12.39846942,13.07487426,13.71329059\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.52747789,14.88471301,15.25704348,15.6371949,16.01797405,16.39328674,16.75846815\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,6.599204889,7.406951551,8.215160056,9.015662009,9.801419415,10.5664938,11.30608598\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.734352254,8.541159836,9.337573806,10.11904496,10.88066084,11.61783948,12.32675818\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.276005932,8.143019578,8.991018747,9.816012305,10.61421576,11.38223107,12.11728243\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,9.29460338,10.12316494,10.91612135,11.67175688,12.38911418,13.0678433,13.70811534\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.56715207,14.91166731,15.27417945,15.64672168,16.02159655,16.39233672,16.75399546\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,6.712863489,7.533122979,8.351102969,9.158872222,9.949661097,10.71780934,11.45879544\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.697998388,8.508088479,9.307450608,10.09150312,10.85536711,11.59451316,12.30516937\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.289935051,8.154993991,9.000676511,9.82323276,10.61904125,11.38480861,12.11782011\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,9.285675597,10.11271253,10.90447397,11.65917185,12.37580552,13.05399854,13.6939029\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.51639747,14.86827366,15.23620713,15.61295718,15.99124968,16.36486463,16.72900247\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,6.652851024,7.468531932,8.282492717,9.086444347,9.873486463,10.63798879,11.37553669\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.732740729,8.544175064,9.345448893,10.13153051,10.89723555,11.63786016,12.34955741\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,7.328549944,8.193766472,9.039192687,9.861100051,10.65594101,11.42050671,12.15215983\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,9.29818811,10.12428666,10.91521006,11.66919594,12.38524363,13.06296004,13.70247416\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.54507268,14.89979247,15.27008071,15.64855586,16.02794635,16.40209912,16.76630433\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,15.26947374,16.00590768,16.66592155,17.25992238,17.79650191,18.28275599,18.72458602\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.33405728,15.17620692,15.93881863,16.62903423,17.25359584,17.81880174,18.33048011\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.27564621,15.27848851,16.15636346,16.92723876,17.6064424,18.20689847,18.73947654\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,17.36345394,17.87458539,18.33749345,18.76040673,19.14819032,19.50410623,19.83069189\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,15.13879044,15.89457007,16.57055299,17.17761786,17.72485501,18.2198192,18.66880406\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.19036372,15.08891075,15.89522191,16.61916446,17.26959369,17.85445836,18.38088716\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,13.72137622,14.76006893,15.6758364,16.48424575,17.19926341,17.83312012,18.39640518\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,16.96083894,17.5194779,18.02031148,18.47416346,18.88769511,19.26541729,19.61074648\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,15.18517099,15.89308448,16.53111825,17.10824503,17.63204854,18.10889489,18.54412608\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.90955422,15.75021544,16.50185871,17.17517145,17.77927143,18.32205576,18.81043282\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.01740793,15.02192021,15.9069808,16.68826737,17.37957782,17.99283877,18.53828632\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,16.48516845,17.07748944,17.61198978,18.09807236,18.54174571,18.94729536,19.31814867\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,15.14890986,15.90029459,16.57312692,17.17810361,17.72408131,18.21839223,18.667144\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.35977902,15.20303543,15.9657443,16.65543173,17.27909032,17.84318221,18.35364262\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.22488746,15.22962068,16.11000448,16.88364175,17.56565134,18.1688409,18.70401847\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,17.66569401,18.13306242,18.56089423,18.95532873,19.31970648,19.65616821,19.96641746\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,15.28593929,16.02241141,16.682368,17.27600265,17.81189494,18.29721019,18.73793917\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.47422592,15.34804103,16.13136152,16.83431685,17.46578952,18.03363379,18.54482718\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,13.65790319,14.70661803,15.63056308,16.44563931,17.16610699,17.80444013,18.37142361\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,17.2714815,17.78612234,18.25147741,18.67638526,19.0660347,19.42384097,19.7523986\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.97812192,15.70847475,16.36526037,16.95832991,17.49586873,17.98467022,18.43039105\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,14.5957497,15.46787585,16.24713391,16.94471715,17.57018461,18.13181694,18.6368552\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,13.8754717,14.89266406,15.78971617,16.58200623,17.28324472,17.90538026,18.45872266\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe], topology \",,,16.56287134,17.143585,17.66892363,18.14763561,18.58528267,18.98583665,19.35249912\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,19.49523107,19.85892735,20.14754287,20.37999205,20.56970692,20.72639965,20.85721223\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,19.26726442,19.66715413,19.98407121,20.23903313,20.44693346,20.6185191,20.76167817\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,2.625240408,3.264353183,3.936670061,4.622979749,5.308606522,5.983201237,6.640027862\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,2.39141899,2.979428454,3.610101781,4.267046853,4.936867773,5.609300805,6.276833594\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,3.143489217,3.785464398,4.455030091,5.134339589,5.80906792,6.468611632,7.105751743\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,3.225986554,3.897407042,4.59112615,5.289285937,5.978000265,6.647322671,7.290757029\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,3.021962148,3.692530395,4.388582012,5.091477659,5.786660463,6.463649986,7.115545788\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,3.111937492,3.756596816,4.4276702,5.107817739,5.783085799,6.443128722,7.080897875\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,2.249729068,2.824670328,3.446195307,4.096560909,4.761027803,5.428240954,6.08993934\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,2.669852643,3.315558756,3.990819557,4.677860368,5.363353226,6.03802026,6.695869486\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,3.057410208,3.691660322,4.355901184,5.032078321,5.705551588,6.3653808,7.00403385\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,3.137922601,3.802791368,4.49218228,5.187995377,5.87605329,6.546124597,7.191459887\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,2.982140453,3.652006478,4.348356867,5.052280691,5.748978943,6.427776903,7.081628825\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,3.138088857,3.78891178,4.465357494,5.149933065,5.828639279,6.491157242,7.130508079\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,6.433545864,7.221887417,8.010615199,8.791603814,9.558090834,10.3044801,11.02628807\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,7.569515927,8.28866222,9.004103648,9.7131059,10.41162906,11.0952316,11.75971778\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.219851233,9.984343269,10.71952871,11.42387365,12.09633772,12.7362897,13.34348302\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.197854334,9.971094056,10.71045022,11.41594925,12.08769358,12.72586167,13.33076107\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,6.417993578,7.228061059,8.043173893,8.852755115,9.647930938,10.42152259,11.16800329\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,7.613878742,8.353946348,9.089488767,9.817125392,10.53229646,11.23023961,11.90663308\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.127041233,9.939320067,10.7154745,11.45485424,12.1570587,12.82197804,13.44983955\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.086503004,9.891166285,10.66323223,11.40101213,12.10330653,12.76941624,13.39914644\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,6.440968012,7.22264401,8.002362238,8.772992439,9.528642495,10.26439271,10.97623482\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,7.592139833,8.309960392,9.024625924,9.733170401,10.43138913,11.11473465,11.77894997\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.229490637,9.993725549,10.72802227,11.4310982,12.10210276,12.74054016,13.34625558\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.185279731,9.959654369,10.70000446,11.40641806,12.07903177,12.71803926,13.3237529\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,6.502855636,7.285721403,8.066831152,8.839031322,9.596360174,10.33380819,11.04727677\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,7.634338467,8.370654069,9.104079566,9.830718711,10.54559937,11.24365657,11.92036063\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.130287386,9.944485202,10.72194432,11.46209222,12.1646408,12.82959196,13.45726899\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,9.065498552,9.873124425,10.64816959,11.38882355,12.09380296,12.76235589,13.39426013\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,16.63103654,17.40474874,18.04745804,18.5870412,19.04475099,19.4368814,19.77602231\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.25025221,15.13109397,15.91368237,16.6109849,17.23380544,17.79128891,18.29127274\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.55202911,15.267285,15.91438615,16.50105958,17.03425344,17.52001469,17.96353705\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.30078228,15.19546416,15.99005995,16.69707512,17.32726374,17.88994461,18.39323221\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.64982916,15.38902574,16.05451523,16.65539372,17.1994434,17.69326359,18.14245881\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,16.76313455,17.52662374,18.15959884,18.68991468,19.1388441,19.52270691,19.85411164\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.2946415,15.15468799,15.91932643,16.60150388,17.211862,17.75929761,18.25135925\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.5579268,15.25911894,15.89533173,16.47358683,17.00029904,17.48111102,17.92090758\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.51997225,15.34054832,16.07248416,16.72739488,17.31497676,17.84339866,18.31961493\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes O, [Co], topology rna\",,,14.78140741,15.48458384,16.11845197,16.69185494,17.21231195,17.6861306,18.11859539\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,18.98856705,19.3189965,19.58410827,19.79959997,19.97683566,20.1241736,20.24785254\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,18.97210135,19.30735775,19.57577148,19.79356329,19.97242771,20.12093612,20.24546732\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.270598188,3.940923019,4.620362796,5.295459439,5.956512111,6.597092556,7.213410979\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.01801311,3.634223345,4.266366651,4.902239237,5.532368961,6.149920676,6.750347129\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.262548148,3.932325647,4.611426833,5.286357357,5.94737995,6.588033771,7.204501644\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.011705701,3.62789882,4.260155784,4.896233438,5.526627419,6.14447793,6.745219796\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.279036823,3.94974431,4.629499519,5.304842196,5.966068033,6.60674809,7.223095447\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.018988919,3.634551634,4.266038667,4.901286645,5.530848534,6.147902355,6.747905449\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.272743005,3.94323873,4.622874825,5.298177825,5.959431265,6.600194424,7.216669263\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,3.012795333,3.628409986,4.260042465,4.895500215,5.525312568,6.142639266,6.742924088\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,6.265270086,7.014485871,7.769953232,8.52395406,9.269583153,10.00074955,10.71228351\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.458920792,10.22051276,10.94095681,11.62243008,12.2669559,12.87639275,13.45243791\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.69450193,10.42042269,11.10091122,11.74226736,12.34904679,12.924456,13.47074392\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,6.245204857,6.994417277,7.750098154,8.504474583,9.250592325,9.982321841,10.69446483\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.4422839,10.20383755,10.92453166,11.60646252,12.25158627,12.86170772,13.43848301\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.682584256,10.40937422,11.09075255,11.7329658,12.34054483,12.91668656,13.46363851\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,6.263730701,7.013275259,7.769231491,8.523810936,9.270051996,10.00182196,10.71392262\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.46153402,10.22290253,10.94307682,11.62428204,12.26856167,12.87778131,13.45363925\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.691473018,10.4174786,11.09793126,11.73920169,12.34588675,12.92121515,13.46744631\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,6.246583224,6.996445001,7.752885289,8.508056814,9.254953034,9.98740799,10.70019992\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.451425223,10.21221684,10.93208111,11.61319361,12.25755239,12.86698139,13.44314249\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,9.676767898,10.40345715,11.08478013,11.72698295,12.33459389,12.91080569,13.45786057\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,14.84795946,15.60485665,16.27749385,16.87879819,17.41888554,17.90581863,18.34615637\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,12.89105652,13.78663554,14.58996659,15.31242288,15.96383132,16.55260761,17.08595551\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,14.78747647,15.5493957,16.22634179,16.83142481,17.37487896,17.8648454,18.30793693\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,12.85638992,13.75307294,14.55780658,15.28183045,15.93487707,16.52529782,17.06025426\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,14.26732697,15.08758016,15.81527569,16.46438152,17.04601237,17.56912785,18.04106696\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,13.47946069,14.31124099,15.05963628,15.73471227,16.3451171,16.89825725,17.40049232\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,14.86261314,15.61598195,16.286455,16.88646866,17.42581597,17.91234721,18.35248253\n\"linker [O-]C(=O)C=CC=CC(=O)[O-], nodes [Co], topology bex,pcu\",,,12.98262561,13.86302685,14.65400401,15.36637325,16.00951017,16.59147181,17.11917853\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,20.48677771,20.86427562,21.16029388,21.39633885,21.58737011,21.74401771,21.87398397\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,20.48837721,20.86565115,21.16148592,21.39737964,21.58828532,21.74482787,21.87470556\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.298166732,3.900461144,4.528470944,5.167403968,5.805033558,6.4319944,7.041635723\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.536931393,4.203597225,4.890458288,5.580007578,6.258847841,6.917543741,7.550065033\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.438536349,4.100324461,4.785316252,5.475286184,6.156179533,6.818013376,7.454327522\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.11989866,3.725618394,4.36154878,5.011391597,5.661631678,6.301923947,6.924937609\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.884089355,4.429134938,4.993812762,5.569291684,6.147152129,6.720267129,7.283136981\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.982893454,4.526106423,5.090436883,5.666416783,6.245091023,6.818937666,7.382198102\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.296963291,3.899162605,4.527119786,5.166034078,5.803670514,6.430656628,7.040335909\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.536886547,4.203510401,4.890335618,5.579855494,6.258672359,6.91735015,7.549857801\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.439560862,4.101333685,4.786301123,5.476239035,6.157094614,6.818886883,7.45515738\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.119033744,3.724679713,4.360553775,5.010357007,5.660572594,6.300853392,6.923866454\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.884004212,4.429029676,4.993688186,5.569148436,6.146991107,6.720089674,7.282944899\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.98247142,4.525635366,5.089919478,5.665857413,6.244495222,6.818311542,7.381547846\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.298211225,3.900525695,4.528547567,5.167486751,5.805118332,6.432078355,7.041717054\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.537198953,4.203882303,4.890755126,5.58031101,6.259153505,6.917848121,7.550365396\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.438836538,4.100678373,4.785713154,5.475716099,6.156633413,6.818483243,7.454806534\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.120317111,3.72606564,4.36201143,5.011859652,5.662097828,6.302382973,6.925385892\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.884178929,4.429197947,4.993859513,5.569328894,6.147184076,6.720296482,7.283165373\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.982480374,4.525746402,5.090130766,5.666162193,6.244883631,6.818772155,7.382068851\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.296906215,3.899098422,4.527045061,5.165947418,5.80357198,6.430547204,7.040217082\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.536880489,4.203489444,4.890300982,5.579808928,6.258615854,6.917285723,7.549787363\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.439428339,4.10123123,4.78622566,5.476187695,6.15706455,6.818875282,7.455161537\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.119464299,3.725158525,4.361063105,5.010882775,5.661103967,6.30138227,6.924386955\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.884577618,4.429601009,4.994258361,5.569716713,6.147555766,6.720648528,7.283495655\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,3.982081209,4.52531979,5.089673223,5.665673619,6.244366295,6.818229815,7.381506034\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.233400853,9.957203377,10.66924097,11.36410591,12.03713338,12.68461747,13.30386741\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.683639516,10.41439185,11.12514328,11.81239165,12.47315682,13.10516536,13.70689523\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.753366003,10.47729248,11.18342534,11.86760073,12.52631498,13.15690326,13.75756535\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.254143455,9.98687619,10.70533683,11.40475583,12.08094075,12.73053031,13.35108649\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,7.641348131,8.390887547,9.140370756,9.883607144,10.61437651,11.3270117,12.01675983\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,8.24657303,8.990022695,9.717342651,10.42950673,11.12524344,11.80204211,12.45701237\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.273506632,9.987209402,10.67645121,11.34171987,11.98269063,12.59864672,13.18879787\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.340746209,10.05277626,10.74117406,11.40606202,12.04684189,12.66260666,13.25244501\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.234634477,9.958313391,10.67022618,11.3649679,12.03787651,12.68524835,13.30439423\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.683281572,10.41403181,11.12476793,11.81199203,12.4727277,13.10470469,13.70640343\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.754720124,10.47847958,11.18446322,11.86850338,12.52709436,13.15757031,13.75813046\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.253186994,9.985930559,10.70438896,11.40379689,12.07996588,12.72953804,13.35007785\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,7.641847343,8.391307751,9.140716249,9.883884246,10.61459229,11.3271733,12.01687413\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,8.24661592,8.990116377,9.717470228,10.42965607,11.12540575,11.80221094,12.45718308\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.27358796,9.987188739,10.67626721,11.34133105,11.98207427,12.59779617,13.18771912\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.341747287,10.05369981,10.74195347,11.40665802,12.04723553,12.66279389,13.25243225\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.232771672,9.95664954,10.66875266,11.36367513,12.03675339,12.68428241,13.3035721\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.684129966,10.41484405,11.12557162,11.81280653,12.47356516,13.10557134,13.70730097\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.7523803,10.47645091,11.18271041,11.86699814,12.52581212,13.15648858,13.75722815\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.252614525,9.985469216,10.70403326,11.40354311,12.0798098,12.72947412,13.35009925\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,7.641427778,8.391082328,9.140670343,9.883998887,10.61484663,11.3275463,12.01734569\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,8.247320736,8.990832818,9.718234247,10.43048518,11.12630469,11.80317627,12.45820656\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.274998392,9.988514504,10.6776315,11.34282044,11.98374341,12.59967331,13.18981205\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.340670131,10.05278736,10.74126452,11.40621921,12.04705208,12.66285699,13.25272426\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.234189611,9.957915093,10.66986668,11.36464141,12.03757856,12.6849754,13.30414341\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.683688062,10.41438465,11.12507972,11.81227286,12.47298534,13.10494491,13.70663043\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.753548607,10.47748991,11.18363213,11.86781154,12.52652478,13.15710768,13.75776087\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.251318691,9.984253929,10.70288138,11.40244037,12.07874509,12.72843933,13.34908883\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,7.642127338,8.391661037,9.141134877,9.884358777,10.61511267,11.32772958,12.01745701\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,8.247296723,8.990864197,9.718296829,10.43056277,11.12638667,11.80325588,12.45827972\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.274539721,9.988075115,10.67712787,11.34219491,11.98296052,12.59871588,13.188677\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,9.341398946,10.05348729,10.74186402,11.40667659,12.04734663,12.66298258,13.25268474\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,10.46819714,11.25273813,12.01009415,12.7373847,13.43185651,14.09138845,14.71468051\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,10.4699123,11.25420101,12.01133952,12.73844343,13.43275556,14.09215113,14.71532689\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,10.46789728,11.25253551,12.00995197,12.73727742,13.43176708,14.09130594,14.71459832\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,10.46976977,11.25417845,12.01139862,12.73855657,13.43290305,14.09231908,14.71550562\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,16.07663095,16.71217584,17.26777669,17.76065821,18.20323473,18.60442571,18.97068937\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,15.41960237,16.13674372,16.75985778,17.30925138,17.799619,18.24159184,18.64293326\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,16.05175033,16.6904787,17.24867191,17.74368364,18.18802769,18.59070015,18.95821824\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,15.39543895,16.11549987,16.74107167,17.29253407,17.78464862,18.22810419,18.63071202\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,16.10889221,16.74039242,17.29265621,17.78275672,18.22299381,18.6221994,18.98676417\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,15.41454448,16.13198901,16.75542277,17.30513037,17.79579546,18.23804468,18.6396402\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,16.06695395,16.70386247,17.26054412,17.75428975,18.19756445,18.5993262,18.9660624\n\"linker O=C[C](c1ccncc1)C=O, nodes [Co], topology rtl\",,,15.38283083,16.10415614,16.73085824,17.28332201,17.77632004,18.22055406,18.62384811\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,20.44752489,20.94938359,21.35198461,21.67939465,21.94893834,22.17329954,22.36191296\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,20.44556102,20.94769157,21.35051671,21.67811257,21.94781131,22.1723027,22.36102618\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,20.44531467,20.94749448,21.35035625,21.67797986,21.94769998,22.17220814,22.36094495\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,20.44808084,20.94985615,21.3523903,21.67974614,21.94924546,22.17356994,22.3621527\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,20.44479404,20.94703694,21.34995248,21.6776219,21.94738113,22.17192278,22.36068841\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,20.4454025,20.94756661,21.3504163,21.67803047,21.94774313,22.1722453,22.36097726\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437397267,4.090890906,4.767564442,5.4500772,6.124784887,6.78180854,7.414617929\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437839072,4.091155088,4.767614222,5.449898338,6.124381101,6.781195955,7.413820028\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.44115929,4.095072346,4.772055774,5.454776923,6.129604835,6.78667555,7.419473419\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437492736,4.091000553,4.76768659,5.450209089,6.124923454,6.781950888,7.414761563\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437954191,4.091304285,4.767791468,5.450097124,6.124595211,6.781419895,7.414049202\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.441326564,4.095288972,4.772316079,5.455073351,6.129929281,6.787020244,7.419831412\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.441100887,4.095011715,4.771993808,5.454714149,6.129541614,6.786612184,7.419410189\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.43760029,4.091110951,4.767798,5.450320709,6.125034961,6.782062121,7.414872367\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437737293,4.091045639,4.767498718,5.449778569,6.124258795,6.781072651,7.413697025\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.44125907,4.095203068,4.772211413,5.454950993,6.129791253,6.786869078,7.419669802\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437700954,4.091246719,4.767967556,5.45052001,6.125258658,6.782304551,7.41512816\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.43775386,4.091080241,4.767549835,5.449843499,6.12433444,6.781156006,7.41378543\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437474717,4.090968071,4.76764042,5.450151222,6.124856368,6.781877077,7.414683277\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437754863,4.091067799,4.767525217,5.449808854,6.124292178,6.78110842,7.413734509\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.441112622,4.0950257,4.772010018,5.454732664,6.129562462,6.786635287,7.419435364\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437434116,4.090941598,4.767628597,5.450152935,6.124869686,6.781899813,7.414713315\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437946282,4.091299355,4.767788517,5.450095464,6.124594371,6.781419563,7.414049168\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.441291332,4.095247102,4.772269645,5.455024012,6.129878331,6.786968666,7.419779941\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.441174772,4.095090809,4.772075701,5.454797014,6.129624109,6.786693349,7.419489357\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437519912,4.091025723,4.7677097,5.450230963,6.124945145,6.781973332,7.414785441\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437776141,4.091088781,4.767545332,5.449827775,6.124309753,6.781124616,7.413749365\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.441229109,4.095168874,4.772173397,5.454909803,6.129747628,6.786823748,7.419623439\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437706036,4.091257848,4.767983277,5.450539175,6.125280364,6.782328087,7.41515296\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,3.437794753,4.091118198,4.767585188,5.449876494,6.124365278,6.781184858,7.413812452\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711227185,10.48030727,11.22304373,11.93645362,12.61839686,13.26746027,13.88288693\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.710655215,10.47979913,11.22259323,11.93605176,12.61803428,13.26712849,13.88257889\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.709780661,10.47896993,11.2218156,11.93532924,12.6173682,13.26651842,13.88202306\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711646143,10.4807098,11.22342938,11.93682172,12.61874686,13.26779191,13.88320023\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.710552464,10.47974119,11.22257091,11.93605724,12.61806104,13.26717124,13.88263335\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.709662104,10.47888737,11.22176323,11.93530134,12.61735957,13.26652461,13.88204041\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.70992019,10.47911712,11.22196896,11.93548722,12.61752928,13.2666812,13.8821863\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711325774,10.48038668,11.22310268,11.9364924,12.6184167,13.26746292,13.88287437\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.71044926,10.47960171,11.22240266,11.9358672,12.61785537,13.26695513,13.88241108\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.70963389,10.47887515,11.22176406,11.93531286,12.61737984,13.26655203,13.88207359\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711684273,10.48073967,11.22345165,11.93683708,12.61875602,13.26779557,13.88319908\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.71069861,10.47985567,11.22265876,11.93612302,12.6181087,13.26720414,13.8826543\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711332545,10.48039857,11.22312113,11.93651773,12.61844863,13.26750083,13.88291749\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.710559315,10.47971148,11.22251271,11.93597771,12.61796625,13.26706609,13.88252173\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.709761224,10.47894642,11.22178719,11.93529588,12.61733025,13.26647647,13.88197781\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711671124,10.48073277,11.22344993,11.93683986,12.61876279,13.26780588,13.88321252\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.710275686,10.47947939,11.22232162,11.9358189,12.61783267,13.26695217,13.88242314\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.709899675,10.47910176,11.2219563,11.93547502,12.61751575,13.26666511,13.88216691\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.709830286,10.47903984,11.22190353,11.93543249,12.617484,13.26664414,13.88215633\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711336933,10.48040238,11.2231229,11.93651675,12.6184446,13.26749375,13.8829075\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.710538834,10.479693,11.2224971,11.93596517,12.61795662,13.26705911,13.88251705\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.709578794,10.47883072,11.22173033,11.93528921,12.61736533,13.26654558,13.88207409\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.711489119,10.48056567,11.22329651,11.93669856,12.61863207,13.26768434,13.88309898\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,9.710930798,10.4800725,11.22286294,11.93631628,12.6182922,13.26737868,13.88282048\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.86848552,7.708347173,8.546943902,9.374172932,10.18202277,10.96425311,11.71620066\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219364123,8.956828584,9.690789117,10.41745487,11.13184251,11.82884455,12.50390255\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868745894,7.708460032,8.546953426,9.374112131,10.18191613,10.96411852,11.71605098\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219140529,8.956507226,9.690371664,10.41694753,11.13125492,11.82818832,12.50319007\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868399884,7.708255927,8.546826122,9.374017878,10.18182664,10.96401658,11.7159271\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219336639,8.956821496,9.690796441,10.41747207,11.13186621,11.82887224,12.50393242\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868712623,7.70872071,8.547445658,9.374782517,10.18271941,10.96501703,11.71701397\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219398106,8.956870711,9.690836899,10.41750611,11.13189543,11.82889777,12.50395506\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868969346,7.708875407,8.547543091,9.374853453,10.18278426,10.9650886,11.71709964\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219019045,8.956427129,9.690324404,10.41692613,11.13125371,11.82820277,12.50321655\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868879321,7.708944193,8.547710166,9.375076496,10.18303401,10.96534529,11.71735034\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219629688,8.95709031,9.691045382,10.417704,11.13208308,11.82907546,12.50412307\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868237378,7.708141755,8.546770387,9.374023331,10.1818912,10.96413525,11.71609338\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219265257,8.956752826,9.690728793,10.41740434,11.13179781,11.82880296,12.5038623\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868143265,7.708042558,8.546645067,9.37386128,10.18168882,10.9638934,11.71581556\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219272538,8.956765651,9.690742497,10.41741607,11.13180598,11.82880685,12.50386175\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.86833475,7.708124719,8.546676871,9.373881565,10.18172186,10.96395313,11.71590876\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219067236,8.95645656,9.690334391,10.41691747,11.13122808,11.82816225,12.50316337\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868497812,7.708551992,8.547311403,9.374674035,10.18263022,10.96494231,11.71695016\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219334781,8.95682777,9.690807427,10.41748518,11.13187963,11.8288848,12.50394341\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868858199,7.708911249,8.547671447,9.375035216,10.18299187,10.9653032,11.7173088\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219492627,8.956971961,9.6909407,10.41760926,11.13199563,11.82899344,12.50404525\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,6.868516014,7.708507712,8.547234446,9.374585792,10.18254529,10.96487001,11.71689584\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,8.219020606,8.956440284,9.690341249,10.41694161,11.13126483,11.82820797,12.50321524\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74031953,15.58346417,16.33662391,17.01082755,17.61571632,18.1596301,18.6497627\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.75223043,15.59389308,16.34584085,17.01903881,17.62308225,18.1662774,18.65579302\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73758605,15.58095069,16.33433485,17.00875344,17.61384108,18.15793519,18.64822944\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74750114,15.58981428,16.34228432,17.01590989,17.62030891,18.16380344,18.65357367\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74879613,15.59095587,16.34330976,17.01684263,17.6211645,18.16459281,18.65430495\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73544908,15.57929581,16.33305796,17.00777539,17.61310063,18.15738433,18.64783015\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74529653,15.5876463,16.34020482,17.01394363,17.6184651,18.16208256,18.65197148\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73492167,15.57857109,16.3321704,17.00675912,17.61198705,18.15620107,18.64660071\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74233091,15.58507159,16.33794296,17.01193565,17.6166662,18.16045833,18.65049519\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73208783,15.57621937,16.33023542,17.00517872,17.61070513,18.15516853,18.64577544\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74078195,15.5838206,16.33691087,17.01106896,17.61592757,18.15982097,18.64993936\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73898959,15.58224455,16.33555361,17.009917,17.6149604,18.15901595,18.64927431\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73355984,15.57742908,16.33121137,17.00595216,17.6113065,18.15562571,18.64611303\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74578844,15.58809986,16.34062475,17.01433289,17.61882595,18.16241703,18.65228152\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73125915,15.57532069,16.32930828,17.0042494,17.60979017,18.1542782,18.6449159\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74168555,15.58460342,16.33760441,17.01169467,17.61650012,18.1603505,18.65043296\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73839635,15.58180673,16.3352107,17.00963149,17.61470931,18.15878543,18.6490562\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73500307,15.57873755,16.33244386,17.00714091,17.61246773,18.1567663,18.64723469\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74782658,15.58998726,16.34235348,17.01590735,17.62025646,18.16371625,18.6534625\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73873001,15.58201777,16.33529242,17.00959173,17.6145626,18.15854862,18.64874601\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74947824,15.59145657,16.34366487,17.01708104,17.62130969,18.16466389,18.65431748\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73587727,15.57966583,16.3333694,17.00803095,17.61330485,18.15754267,18.64794834\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.73831226,15.58183718,16.33529372,17.00973219,17.61480877,18.15887406,18.64912981\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,14.74770475,15.58994049,16.34238645,17.01601512,17.62042966,18.16394399,18.65373402\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,13.85577858,15.05386137,16.10010816,17.00969838,17.79933311,18.48520409,19.08204594\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe][O]([Fe])[Fe], topology acs\",,,13.85577289,15.05384318,16.10008197,17.0096674,17.79929954,18.48516943,19.08201119\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,20.1690596,20.56383298,20.87743542,21.1302224,21.33667593,21.50728479,21.64977363\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,20.16861542,20.56345067,20.87710398,21.12993297,21.33642141,21.5070595,21.64957299\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.918054068,4.621823435,5.330722243,6.030022921,6.709262242,7.361565582,7.982937901\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.665298889,4.3730329,5.093967316,5.810174171,6.508758454,7.18118137,7.822407226\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.476020298,4.173410778,4.892270715,5.612370106,6.318716697,7.001087974,7.653198968\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,2.557917605,3.025701784,3.53059488,4.064219599,4.617282747,5.180865632,5.7471923\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,2.707818227,3.196723338,3.721173616,4.271894301,4.839092437,5.413688205,5.987992909\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,4.917566176,5.326214887,5.759646776,6.212359984,6.677886431,7.149880647,7.622764039\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.038989249,5.447563016,5.88052701,6.332305812,6.796450184,7.266689636,7.737549484\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.626887859,5.988243024,6.380229774,6.796271371,7.229011917,7.671419707,8.11740908\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,4.902466545,5.31144944,5.743697225,6.194585458,6.658123201,7.128204256,7.599350406\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.067440148,5.490880124,5.934476703,6.39393815,6.863627814,7.337825548,7.811454514\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.125416943,5.530357694,5.957953948,6.403913122,6.862454893,7.327636796,7.79412557\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.297621139,3.954098235,4.635422511,5.323699254,6.004819457,6.668554202,7.308130183\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.144556085,3.775459739,4.436063956,5.108669996,5.778902871,6.436016432,7.072617535\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.354364169,4.011799451,4.694184829,5.383412346,6.065219386,6.729290017,7.368820172\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.443656343,4.106509433,4.791654673,5.481447541,6.162110823,6.823765046,7.459967093\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.918044991,4.621819541,5.330722664,6.030026859,6.70926899,7.361574531,7.982948538\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.665328343,4.373066478,5.094003805,5.810212529,6.508797825,7.181221073,7.822446734\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.475940538,4.173328333,4.892187701,5.61228815,6.318636961,7.001011232,7.653125691\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,2.557968518,3.025752148,3.530644371,4.064268021,4.617329996,5.180911672,5.747237155\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,2.707893827,3.196801537,3.721253899,4.27197604,4.839174945,5.413770781,5.988074876\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,4.91756861,5.326221048,5.759656211,6.212372159,6.677900818,7.149896767,7.622781483\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.039246117,5.447822968,5.880789096,6.332568419,6.796711377,7.266947388,7.737801815\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.626692938,5.9880344,6.38001056,6.796044672,7.228780762,7.671186966,8.117177405\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,4.902556573,5.311540111,5.743788934,6.194678103,6.658216402,7.128297502,7.599443149\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.067540907,5.490973498,5.934563763,6.394019678,6.863704403,7.337897659,7.811522519\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,5.125463278,5.530397983,5.957989092,6.403943792,6.86248164,7.327660105,7.794145884\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.297678597,3.954161458,4.635489903,5.323769335,6.004890949,6.668626053,7.308201562\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.144536862,3.775441737,4.436047684,5.108655715,5.778890657,6.436006231,7.072609218\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.354350099,4.011780302,4.69416157,5.383385964,6.065190795,6.729260012,7.368789422\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,3.443488477,4.106331484,4.791470501,5.481260503,6.161923674,6.823579951,7.459785689\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,8.905083451,9.567130402,10.23529764,10.90150794,11.55830254,12.19935106,12.81965513\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.5855462,10.27325062,10.95644749,11.62838631,12.2830506,12.91555258,13.52225215\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.454592372,10.12940897,10.8054678,11.47488185,12.13051451,12.76649814,13.37839109\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,8.587001046,9.56325805,10.49303322,11.36990536,12.19080793,12.9551205,13.66393668\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.088997859,7.934671694,8.768585831,9.584421335,10.37671162,11.14095122,11.87367604\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.552582493,8.339799373,9.117804099,9.882804852,10.63031111,11.3558855,12.05565568\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.550273123,8.338819543,9.118413805,9.885012711,10.63398768,11.3608354,12.0616617\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,12.53179788,13.22187772,13.86525814,14.46515556,15.02392295,15.54361696,16.02628744\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,12.51469847,13.21669452,13.86721093,14.47115292,15.03198328,15.55248791,16.03519528\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,6.463417647,7.24712212,8.029706057,8.803772691,9.563393906,10.30368426,11.02065534\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.873449177,8.604238449,9.333394952,10.05678769,10.76924246,11.46552148,12.14095056\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.450022958,10.22826565,10.97824755,11.69754599,12.38437871,13.03757478,13.65655012\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.517792559,10.28519452,11.02580264,11.73707756,12.41708087,13.06447833,13.67853286\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,6.796591643,7.551539617,8.307094871,9.056120217,9.792732828,10.51198963,11.20980046\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.906713579,8.645172391,9.380252714,10.10786366,10.823007,11.52068306,12.19646894\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.469542862,10.24064816,10.98455165,11.69878212,12.38147862,13.03136674,13.64774855\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.449360928,10.22399668,10.97180813,11.68991349,12.37621673,13.02932749,13.64850681\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,8.905063118,9.567111393,10.23527973,10.90149089,11.55828615,12.19933516,12.81963961\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.585554879,10.27326577,10.95646767,11.62841027,12.28307728,12.91558111,13.52228181\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.454598265,10.12941467,10.80547302,11.47488638,12.13051828,12.76650114,13.37839335\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,8.587045404,9.563300603,10.49307449,11.36994566,12.1908474,12.95515918,13.66397455\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.089028385,7.934703318,8.768619187,9.584456704,10.37674901,11.14099046,11.87371685\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.552538816,8.339759459,9.117767892,9.882772139,10.63028161,11.3558589,12.05563168\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.550322047,8.338867496,9.118462191,9.885062329,10.63403886,11.36088816,12.06171583\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,12.5317627,13.2218526,13.86524097,14.46514467,15.023917,15.54361489,16.02628839\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,12.51476155,13.21675464,13.86726876,14.47120881,15.03203735,15.55254021,16.03524579\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,6.463473482,7.247177436,8.029759757,8.803824117,9.563442696,10.30373025,11.02069851\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.873434096,8.604230674,9.333394479,10.05679412,10.76925513,11.4655396,12.14097329\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.450059958,10.2283015,10.97828232,11.69757972,12.3844114,13.03760644,13.65658073\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.517820261,10.28522393,11.02583302,11.73710834,12.41711162,13.06450871,13.67856263\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,6.796501097,7.551477393,8.307057946,9.056105033,9.792735728,10.51200714,11.20982946\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,7.906758924,8.645216591,9.380294749,10.10790287,10.82304302,11.52071571,12.19649823\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.469509678,10.2406083,10.98450631,11.69873241,12.38142556,13.03131124,13.64769141\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.449367132,10.22400077,10.97180952,11.68991206,12.37621264,13.02932102,13.64849829\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,10.25628727,10.960095,11.66279983,12.35611446,13.03248808,13.68576442,14.3113803\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.295844438,9.944449857,10.59283998,11.23926295,11.87954494,12.50867106,13.12179509\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,10.2562655,10.96006844,11.66276922,12.35608052,13.03245149,13.68572582,14.31134026\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,9.295882768,9.944481015,10.5928656,11.23928435,11.87956317,12.50868692,13.12180919\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,14.77337994,15.54530451,16.23850633,16.86276742,17.42648685,17.93681184,18.39982717\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,14.86511758,15.61236424,16.28014096,16.88030726,17.42231412,17.91374702,18.36076681\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,13.97781093,14.83049305,15.60409709,16.3048396,16.93911862,17.5131679,18.03287032\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,16.12935902,16.71218924,17.23780114,17.71500244,18.15061659,18.54997707,18.917307\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,14.77410852,15.54595528,16.23909062,16.86329472,17.42696504,17.93724745,18.40022562\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,14.86345301,15.61089377,16.27883539,16.87914217,17.42126917,17.91280534,18.35991434\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,13.97829056,14.83093141,15.60449982,16.30521126,16.93946295,17.51348797,18.03316868\n\"linker Cc1c(C)c(Cn2cncc2)c(c(c1Cn1cncc1)C)C, [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Zn], topology nbo\",,,16.12929836,16.71209981,17.23769123,17.7148777,18.15048113,18.54983399,18.91715875\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,20.83519572,21.19100279,21.46806321,21.68771165,21.86460596,22.00905646,22.1284708\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,20.66455178,21.04694155,21.34504059,21.58156915,21.77218072,21.92790946,22.05669638\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.5255784,18.23714248,18.8386564,19.34788734,19.78036787,20.14921338,20.46528932\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.53765808,18.24734305,18.8473867,19.3554432,19.78696988,20.15502996,20.47045147\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.448970005,4.076340036,4.724227134,5.378025701,6.025971515,6.659281784,7.271913539\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.846182796,4.545315608,5.255365838,5.959741032,6.646318678,7.306999521,7.93699645\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.800276485,4.49042274,5.194274997,5.894874132,6.579640616,7.240033858,7.870883518\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.379761168,3.986706691,4.619936458,5.264000484,5.906245413,6.537083456,7.149794546\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.234868593,3.839202217,4.471645182,5.116563919,5.760989829,6.39498243,7.011486304\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.550710585,4.226294307,4.923563032,5.623777923,6.312650938,6.980194368,7.620098571\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.709679097,4.381816199,5.069229598,5.755695103,6.428991558,7.080638647,7.705324293\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.172217948,3.76060545,4.381068899,5.017665404,5.656949155,6.288470921,6.904703099\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.271884935,3.881522442,4.5177864,5.165155729,5.810869024,6.445215609,7.061355745\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.515921671,4.189388742,4.88518164,5.584562477,6.273207571,6.941070537,7.581772985\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.763053069,4.452413106,5.156353478,5.857639854,6.543478744,7.205175051,7.837451881\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.296522824,3.889690069,4.511696158,5.147193296,5.783372391,6.410360567,7.021104903\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.366420409,3.985154909,4.627211831,5.277621807,5.924185209,6.557700203,7.17175815\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.792337791,4.484382808,5.189624064,5.891050622,6.576113209,7.236329049,7.866587207\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.690010798,4.373591403,5.071774744,5.767908141,6.449562087,7.108202404,7.738563297\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,3.179885439,3.771547238,4.395359238,5.035126212,5.677217524,6.311067059,6.92908742\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.13737697,14.92661081,15.58375773,16.13706046,16.60945594,17.01911763,17.38019012\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.05898346,14.85664326,15.52134989,16.08127936,16.55940283,16.97397417,17.3392355\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.412897372,10.1630439,10.89500457,11.6044207,12.28761629,12.94174234,13.56482224\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.943892884,10.68805371,11.4089686,12.10310154,12.76780659,13.40126829,14.00242866\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.930845326,10.67263369,11.39305413,12.08846246,12.75580515,13.39278816,13.99792034\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.686810505,10.41290757,11.12715646,11.82364189,12.49725504,13.14399094,13.76101819\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.02738205,14.83081242,15.50024461,16.06405803,16.54538665,16.96261292,17.33008036\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.09364837,14.88941646,15.55210654,16.11004138,16.58625888,16.99903862,17.36262852\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.307808509,10.03078371,10.74202554,11.43651908,12.10966851,12.75769064,13.37776979\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.715468544,10.44282797,11.15201735,11.83912165,12.50078176,13.13439918,13.73818934\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.941481911,10.65840993,11.36166599,12.04572591,12.70595311,13.33882251,13.94192806\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.604705359,10.32509385,11.03448368,11.72701933,12.39762239,13.04227539,13.65809526\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.18479566,14.97042702,15.62417924,16.1743008,16.6437071,17.05054616,17.40894276\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.01754612,14.82101738,15.49067636,16.0548256,16.53655457,16.9542191,17.32214574\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.27536251,10.00332794,10.7191759,11.41776636,12.09449365,12.74561073,13.3683527\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.743551587,10.47488317,11.1885438,11.87988681,12.54519035,13.18171436,13.78765875\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.816819578,10.54764582,11.26066139,11.95152442,12.61655808,13.252955,13.85881575\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.56840385,10.28837892,10.99742423,11.68974352,12.3602859,13.00504159,13.62112221\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.10535056,14.89833365,15.5586412,16.11458281,16.58916698,17.00063594,17.3631972\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,14.12275629,14.91387887,15.5725687,16.12713801,16.60057805,17.01110525,17.37289853\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.391561451,10.13653345,10.86426496,11.57036725,12.25104604,12.90332283,13.52510617\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.900756176,10.64128674,11.35801664,12.04803631,12.70905607,13.33943706,13.93818302\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,10.0125185,10.74126569,11.45450827,12.14669401,12.81326283,13.45083013,14.05716495\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,9.691064624,10.4165005,11.12974702,11.82512122,12.4976658,13.14345804,13.75969997\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,8.188629111,8.922573145,9.651369439,10.37184439,11.07964795,11.77014937,12.43908796\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,8.750223298,9.675397951,10.56222342,11.40790316,12.21045789,12.96868955,13.6821799\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,8.237673767,9.020249765,9.792718635,10.55111884,11.29085387,12.00741915,12.69692491\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,8.071579316,8.800289369,9.526852281,10.24675275,10.9548201,11.64598724,12.31579938\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,7.312909062,8.164995177,9.006875268,9.829613187,10.62659773,11.39303253,12.12560717\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,8.037688403,8.813720265,9.581698768,10.33733529,11.07580948,11.79244454,12.48319749\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.04205185,17.58932895,18.03879023,18.4138276,18.73239532,19.00818628,19.25156261\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.28238027,17.7956958,18.21767115,18.5702777,18.87038708,19.13086484,19.36143671\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.07084856,17.61215469,18.05690959,18.42817349,18.74366941,19.01692719,19.25819236\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.0122221,17.56375612,18.01635128,18.39374592,18.71412647,18.99134359,19.2358682\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.03832952,17.5858181,18.03541608,18.41055414,18.72921015,19.00509066,19.24856483\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.21598862,17.73705616,18.16518999,18.52269391,18.82670242,19.09028994,19.32334959\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.13005002,17.66549211,18.10537111,18.4725982,18.7847576,19.05525571,19.29423093\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,17.09985568,17.64169779,18.08622818,18.45688656,18.77160925,19.044042,19.28448968\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,10.83111892,11.61843715,12.37789784,13.10651553,13.80134902,14.46013217,15.08150519\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,12.41894267,13.31934143,14.1499619,14.91395859,15.6152317,16.25800379,16.8465837\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,11.03600146,11.83270969,12.59814888,13.32955926,14.02444805,14.68105831,15.29852074\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,10.55960144,11.3458461,12.10277223,12.82836795,13.52049698,14.17745169,14.79819246\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,12.20390046,13.0727335,13.87960507,14.62667194,15.31686046,15.95345195,16.53987343\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,10.84165864,11.63200591,12.39197363,13.11921261,13.81143902,14.466939,15.08476757\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,15.87822126,16.65264936,17.3232159,17.91076162,18.43056289,18.8939573,19.30953345\n\"linker O=C(c1ccncc1)[N]c1ccncc1, [C]#N, nodes [Ni], [Zn], topology fsc\",,,16.9515455,17.48691232,17.96099641,18.38602258,18.77109921,19.12291253,19.44636278\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,23.31905226,23.44980459,23.5517723,23.63287477,23.69846704,23.75228001,23.79698063\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,23.49115184,23.59792505,23.68054762,23.74580893,23.7982642,23.84106328,23.87644159\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,22.31441628,22.36891503,22.41122103,22.44470847,22.47166419,22.49368088,22.51189463\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,21.72774065,21.87339154,21.98742983,22.07831986,22.1518891,22.21225034,22.26237023\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,4.547946261,5.299537164,6.024462925,6.714581006,7.36597712,7.977465323,8.549561291\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,4.507964906,5.257474626,5.982399353,6.673936455,7.327621585,7.94185292,8.516851157\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,2.996762133,3.673715263,4.361955011,5.045183679,5.712476294,6.357152182,6.975650773\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,3.955725817,4.72833113,5.479958447,6.198270682,6.8771963,7.514756388,8.111492483\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,20.31383855,20.70121627,21.00928225,21.25776278,21.46077806,21.6285918,21.76877859\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,20.95662601,21.24418678,21.47293258,21.65763887,21.80878536,21.93394875,22.03870421\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,19.05772198,19.61213078,20.05836691,20.42184991,20.72125022,20.97042248,21.17976661\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,20.89244816,21.18857488,21.42407429,21.61424004,21.76989412,21.89884515,22.00682978\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.737347057,7.535122202,8.340185964,9.141603164,9.930156277,10.69843115,11.44075545\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.564184551,7.338727749,8.127549657,8.918732443,9.702071406,10.46919409,11.21354164\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.632582175,7.422050704,8.221991878,9.021704869,9.811718681,10.58407882,11.3324629\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.571370978,7.337087689,8.114274311,8.893146254,9.664968515,10.42219434,11.1586013\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.564913244,7.333322307,8.111461262,8.890337619,9.661635629,10.41804776,11.15350047\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.51591172,7.297712711,8.093027483,8.890656809,9.680663057,10.45465678,11.2059232\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.564506241,7.331735493,8.109915649,8.889429717,9.661617846,10.41898761,11.15536827\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,6.555653188,7.309802556,8.080271215,8.856171377,9.627682883,10.38635218,11.1252627\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.8604038,15.66413347,16.39356704,17.05487873,17.65395858,18.19641191,18.68753279\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,15.57983173,16.25454083,16.85946126,17.40556799,17.90121885,18.35294228,18.76595551\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,13.79458198,14.70622358,15.53727507,16.29221788,16.9760743,17.59429128,18.1524958\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,13.99688082,14.93794771,15.78901514,16.5560732,17.24572753,17.86487625,18.42038387\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,15.47301659,16.13104608,16.73231253,17.28275804,17.78733936,18.25033365,18.67550265\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.03254375,14.94755172,15.77769718,16.52834741,17.20546193,17.81530151,18.36413899\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,15.15245609,15.89726463,16.57301242,17.18662297,17.74417737,18.25110284,18.71228379\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,13.91004423,14.84132345,15.68098311,16.43718249,17.11765363,17.72973947,18.28034551\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.39215884,15.25329521,16.03072272,16.73290231,17.36714967,17.94005187,18.45763979\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,15.92980775,16.59579197,17.20640172,17.76640149,18.27951647,18.74908049,19.17828889\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.55168506,15.28389898,15.96748883,16.6019474,17.18797572,17.72727149,18.22222822\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.73758608,15.50348133,16.19351791,16.81780133,17.38434227,17.89969242,18.36934547\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,18.90763739,19.52018786,20.01640475,20.424443,20.76454088,21.05147748,21.29621361\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.88037551,15.690532,16.41910048,17.07601073,17.6692978,18.20574217,18.69124076\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.91001543,15.67711678,16.36575175,16.98694622,17.54927489,18.05965779,18.52384699\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,13.3805684,14.29488381,15.13426349,15.9012471,16.59948082,17.2334319,17.80802972\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.72143705,15.53467059,16.27352208,16.9441286,17.55217173,18.10307622,18.6020278\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,13.79052875,14.69304327,15.51827218,16.26943666,16.95083684,17.56749501,18.12477699\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,15.35512259,16.05588357,16.69455175,17.27722212,17.8091445,18.29497626,18.73891179\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,15.07453608,15.82842846,16.50922508,17.12604721,17.6860734,18.19524201,18.65864727\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.5431396,15.33399238,16.05664088,16.71667918,17.31896665,17.86803274,18.36821307\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.91099735,15.68897997,16.39759771,17.04268511,17.62944479,18.1627594,18.64727533\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,15.10535797,15.81502501,16.46486911,17.06083085,17.60749602,18.10877195,18.56820386\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.75256951,15.54862401,16.27712876,16.94173229,17.54650199,18.09582531,18.5942252\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,14.81046334,15.5560886,16.23242763,16.84764383,17.40834119,17.9200519,18.3875387\n\"linker [O-]C(=O)[O-], nodes [Cd][OH2][K][OH2][Cd], [K], [Ru][Ru], topology \",,,17.84358986,18.5754364,19.17347963,19.66838049,20.08281152,20.43371464,20.73390045\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,19.97816207,20.28584689,20.52720872,20.71978209,20.87574501,21.00374013,21.11002423\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,20.00589689,20.30903503,20.54686446,20.73664391,20.89036181,21.01652755,21.12130233\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,19.42536492,19.78481901,20.07441852,20.31062835,20.5055032,20.6679676,20.80471041\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,19.44923335,19.80481683,20.09140008,20.32521861,20.51816837,20.67906164,20.81450644\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,4.827168683,5.564203055,6.282109539,6.972780184,7.63108697,8.254231207,8.841235962\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,4.811218818,5.548380177,6.266818692,6.958247847,7.617420939,8.241464154,8.829355193\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,3.798243159,4.491565785,5.198179768,5.900732969,6.586624875,7.247403428,7.877986792\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,3.798799789,4.492262144,5.198951364,5.901537889,6.587436028,7.24820353,7.878765081\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,4.825151452,5.562151037,6.280081579,6.970807991,7.629186875,8.252410848,8.839498032\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,4.822954645,5.560191908,6.278338571,6.969263034,7.627822544,8.251209725,8.838442932\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,3.796927877,4.490701567,5.197684003,5.900539951,6.586679945,7.247660185,7.878405666\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,3.798111648,4.491644952,5.19847312,5.901230548,6.587307407,7.248246453,7.878963967\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.743924169,10.45058882,11.15159773,11.84008093,12.50952969,13.1545494,13.7711453\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.744952878,10.45014929,11.15013734,11.83791052,12.50687,13.15156016,13.76794376\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.065513021,9.717377615,10.37801852,11.03905137,11.69233712,12.33081431,12.94886242\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.052676879,9.70616828,10.36804407,11.03004313,11.68410756,12.32322991,12.94182591\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.752701819,10.45799378,11.15799443,11.84570929,12.51455202,13.15907899,13.77526393\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.748324001,10.45454158,11.15526263,11.84355156,12.51285966,13.15776807,13.7742676\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.05051889,9.704300748,10.36639065,11.02855136,11.68274185,12.32196605,12.94064722\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,9.06125165,9.712995195,10.37356798,11.03458112,11.68788934,12.32642409,12.94455771\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.38195547,11.19687787,11.99262996,12.76143086,13.49670931,14.19375944,14.84978036\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.36116679,11.17709169,11.97379451,12.74350175,13.47964891,14.17753444,14.83435939\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.57133294,11.3586131,12.12672805,12.86876248,13.57894661,14.25314195,14.88885439\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.51371032,11.30499841,12.0767347,12.8220966,13.53536572,14.21243166,14.85081666\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.35403739,11.17201032,11.97038636,12.74144147,13.47865957,14.17738475,14.83485929\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.38878769,11.20374113,11.99936593,12.76794394,13.50294394,14.19968641,14.85538803\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.61409014,11.39618333,12.15986807,12.89812296,13.60508049,14.2765151,14.90985734\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.61196167,11.39404293,12.15773452,12.8960029,13.60297643,14.27442918,14.90779266\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.17258852,10.89233172,11.60778114,12.31176606,12.99709484,13.65767679,14.28895111\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.23599155,10.95001027,11.66062126,12.360443,13.04213293,13.69949223,14.3278822\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.26014621,10.97310477,11.68267207,12.38145177,13.06210224,13.71843263,14.34581418\n\"linker [N]1C=NN=C1, nodes [Cu], topology lim,\",,,10.24553892,10.96072057,11.67210306,12.37236679,13.05423348,13.71156446,14.33977348\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,20.14607413,20.50736481,20.79272154,21.02161797,21.20778542,21.36108965,21.48874444\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,20.13478181,20.49628231,20.78180108,21.01082482,21.19709389,21.35048036,21.47820256\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.368505633,4.04411816,4.741443739,5.442338534,6.132755392,6.802715532,7.44579002\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.406873357,4.070988932,4.757323157,5.448282904,6.13014011,6.793064359,7.430658309\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.18130324,3.839778473,4.522424277,5.211556855,5.893302063,6.557626929,7.197894709\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,1.97912529,2.511025154,3.097934889,3.722223449,4.36732552,5.019195404,5.666826738\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,1.964604494,2.490549169,3.071754254,3.690775183,4.331194133,4.979055877,5.623388105\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.239439944,3.833302579,4.454810586,5.089010355,5.723454788,6.348545211,6.957410058\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.529673823,4.187825459,4.867720247,5.551785917,6.226476748,6.882181733,7.512697298\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.360227902,4.021927971,4.706717527,5.396534176,6.077463453,6.739619421,7.376595348\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.532050903,4.12995587,4.750723185,5.380406151,6.007527787,6.623324697,7.221597252\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.358939417,4.034074146,4.731143498,5.431980747,6.122519199,6.792766453,7.436285277\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.406823785,4.071430695,4.758177269,5.44944821,6.131497722,6.794480449,7.431986713\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.181572258,3.840262676,4.523156672,5.212546741,5.894542157,6.559099636,7.199576935\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,1.978533914,2.510321855,3.097136859,3.721350076,4.3663963,5.018228565,5.665838464\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,1.967083381,2.493369521,3.074887605,3.69417906,4.334819408,4.98285239,5.6273084\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.236054521,3.829789776,4.451231633,5.085415916,5.719884649,6.345029375,6.953970365\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.530276591,4.188387509,4.868227573,5.552229388,6.226851158,6.882484724,7.512928425\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.363555873,4.025368469,4.710208192,5.400023958,6.080912875,6.742999385,7.379885406\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,3.529349585,4.127304743,4.748166683,5.377976336,6.005245118,6.621200116,7.219634523\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,6.270564392,7.042626663,7.814002562,8.578208937,9.329652734,10.06343359,10.77537011\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.444975402,8.221966805,8.986734373,9.736335891,10.4673394,11.17626863,11.85998998\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,8.95949094,9.743272158,10.50471751,11.23926635,11.9433121,12.61432971,13.25082277\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.575049652,8.343772862,9.101226871,9.844393183,10.56974058,11.27369374,11.95302971\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,6.629793634,7.364587038,8.101983456,8.835530579,9.559623433,10.26927851,10.96015928\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.135134038,9.910097966,10.6628988,11.38946854,12.0863355,12.75094596,13.38171401\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.156940866,7.994590898,8.811291922,9.604818095,10.3727247,11.11253627,11.82203457\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,8.958456319,9.745557527,10.50815781,11.24280579,11.94644343,12.61681177,13.25254367\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.217733237,8.227547066,9.213721862,10.16244243,11.06445091,11.91430695,12.70955116\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.283153006,8.280772428,9.257515102,10.19882377,11.09491711,11.93999269,12.73133821\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.059770679,9.766818226,10.46619476,11.15147208,11.81715684,12.45890365,13.0735474\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.510797856,10.22975427,10.93057866,11.60967028,12.26382489,12.89051224,13.48796731\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.311329464,8.09318562,8.86587559,9.625324934,10.3671995,11.08734917,11.7821682\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.539503026,10.26833687,10.97742131,11.66340302,12.3232568,12.95460723,13.55583279\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.112539954,9.813899792,10.50992446,11.1933849,11.85828577,12.49996719,13.11506097\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,6.292866754,7.064580898,7.835879371,8.60021826,9.351943877,10.08610377,10.79847544\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.455897864,8.23266853,8.9971949,9.746548316,10.47730992,11.18601429,11.86953551\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,8.957938846,9.741544626,10.50273053,11.23697856,11.94071413,12.61143469,13.24765853\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.556604496,8.325509376,9.083250988,9.826764054,10.55248031,11.25679773,11.93647585\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,6.596327984,7.330850833,8.06802148,8.801378779,9.525312968,10.23483841,10.92561763\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.122182354,9.897710877,10.65104055,11.37809117,12.07538261,12.74035636,13.37142485\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.161136822,7.998852165,8.815667851,9.60933773,10.37740083,11.11736983,11.8270186\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,8.973623763,9.760929108,10.52369112,11.25846651,11.96220426,12.63265119,13.26844476\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.223473718,8.233327403,9.219518949,10.16823841,11.0702331,11.92006707,12.71528439\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.288255699,8.285953457,9.262777614,10.20416657,11.10033558,11.94547997,12.73688629\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.05446356,9.761410195,10.46069219,11.14588175,11.81148609,12.45316016,13.06773889\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.506398965,10.22509347,10.92569933,11.60460825,12.25861057,12.88517182,13.48252339\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,7.313540677,8.095411577,8.868115683,9.627578056,10.36946379,11.08962212,11.78444693\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.542809838,10.2716087,10.98067805,11.66665915,12.32652218,12.95788808,13.55913267\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,9.114880424,9.816498834,10.51270521,11.19629562,11.86129148,12.50304402,13.11819248\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,10.57749775,11.3123843,12.0275728,12.71880149,13.38226784,14.01502777,14.61511907\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,10.57851353,11.3133848,12.02856453,12.71978906,13.38325431,14.01601505,14.6161083\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,14.34640281,15.05133598,15.68804355,16.26427615,16.78691514,17.26193531,17.69449091\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,14.89804584,15.65754742,16.33297605,16.93751801,17.48139244,17.97267268,18.41787323\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,15.3893308,16.05013914,16.64982976,17.1954045,17.69279661,18.14705381,18.56251077\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,15.62591393,16.24526919,16.80896004,17.32327307,17.79350309,18.22413888,18.61902975\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,14.45581471,15.16175482,15.79932442,16.37630109,16.89958177,17.37515205,17.80817524\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,14.9177412,15.67712638,16.35243143,16.95685934,17.50063795,17.99184434,18.43699369\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,15.37524784,16.03446271,16.63287496,17.17741048,17.67395264,18.12751392,18.54240246\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C1C(c2ccncc2)C(C1c1ccncc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology sql,\",,,15.5433806,16.16026602,16.72201981,17.23479042,17.70377652,18.13339795,18.52745353\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,21.26008155,21.42607754,21.555378,21.65801649,21.74083208,21.8086095,21.86477467\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,21.54805615,21.66890172,21.76277301,21.83712681,21.89701764,21.94596587,21.98648284\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.240884661,3.904343667,4.599206932,5.304232646,6.002993492,6.683760717,7.33886144\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,4.513542199,5.244764013,5.973423458,6.684803824,7.368908322,8.019628762,8.633885744\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.095222307,3.561776928,4.06326516,4.591630155,5.137824712,5.69318834,6.250231838\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,2.997654157,3.450643287,3.939837922,4.457600886,4.995092962,5.543675936,6.095747307\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,2.885936317,3.487187567,4.123876477,4.778522032,5.436517411,6.086622469,6.720822609\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.021382114,3.48536053,3.986472504,4.516085353,5.064571226,5.622756804,6.182737913\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.093918609,3.574411234,4.090049272,4.631726028,5.189658076,5.754747817,6.319309894\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.560293238,4.230291874,4.923755457,5.62149336,6.308954822,6.975941701,7.615941642\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,2.930067547,3.567662989,4.239760989,4.926769398,5.613046073,6.287029277,6.940815489\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.587461129,4.241376284,4.914045331,5.589329469,6.254776543,6.90152279,7.523822049\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.337553399,3.987940638,4.66064053,5.338872004,6.009534901,6.663172166,7.293527558\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.06591341,3.522543879,4.015785534,4.53762182,5.078834312,5.630480133,6.184750588\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.184574917,3.656450527,4.162956219,4.695663782,5.245179978,5.80258773,6.360246121\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.62294604,4.298108246,4.994175115,5.69243671,6.378871136,7.043753553,7.680954061\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.591578231,4.274128669,4.975417118,5.677317413,6.366296758,7.033015823,7.671634219\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.2404451,3.903903847,4.598777284,5.303820781,6.002604384,6.683397183,7.338524673\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,4.507468551,5.238565323,5.967213732,6.678670235,7.362914542,8.01381918,8.628289538\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.09541042,3.561967854,4.063470825,4.591857158,5.138075261,5.693461418,6.250524282\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,2.998275226,3.451361148,3.940665719,4.458542504,4.996144445,5.544827747,6.096986594\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,2.884875583,3.486018227,4.122620859,4.777203661,5.435158526,6.08524272,6.719438543\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.021716695,3.485835038,3.987072619,4.516793129,5.065366361,5.623617791,6.183643011\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.091762581,3.572051194,4.087510584,4.629043785,5.186872096,5.75189875,6.31643659\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.558759404,4.228626079,4.921966215,5.619600757,6.306984256,6.973919554,7.613892655\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,2.927661227,3.564973838,4.236856673,4.923714589,5.609898713,6.283838896,6.937622882\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.587421924,4.24126056,4.913868453,5.58910582,6.254518602,6.901240893,7.523524491\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.340812972,3.991359067,4.664136076,5.342379332,6.013004401,6.666567808,7.296824355\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.065565894,3.522556131,4.016120654,4.538238598,5.07969009,5.631533149,6.185961663\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.182084708,3.65392839,4.160386354,4.693044301,5.242518731,5.79989838,6.357545025\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.621574441,4.296328001,4.992052032,5.690040037,6.376267804,7.04100442,7.678111994\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,3.588965801,4.271015714,4.971894379,5.673476018,6.362222556,7.028785788,7.667314724\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.090931374,9.730179796,10.38825528,11.0535535,11.7154845,12.36520661,12.9958544\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.91705259,9.570789443,10.23366783,10.89733334,11.55388339,12.1965021,12.81973279\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.998617163,9.898850464,10.76887363,11.59873919,12.38262305,13.11777982,13.80366498\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,7.933496673,8.703998718,9.459749401,10.19969387,10.92144421,11.62200416,12.29838791\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.480704491,10.23778892,10.97466462,11.6874011,12.37247091,13.02717059,13.64972668\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,7.7196951,8.51250371,9.288404747,10.04577086,10.78224021,11.49511837,12.18180955\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.96942863,9.881486786,10.76113296,11.59892607,12.38935916,13.1298938,13.82013451\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.132583625,9.768009923,10.42136792,11.08137606,11.73777415,12.38200192,13.00740489\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.921173107,9.597345581,10.27697051,10.95300754,11.61842649,12.26706068,12.89398535\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.596101158,10.33236696,11.05515755,11.75858806,12.43760211,13.08837854,13.70836153\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.514150183,10.27058275,11.00933809,11.72523891,12.41391796,13.072153,13.69787892\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,7.835856646,8.613661772,9.37729258,10.12471474,10.85312716,11.55943651,12.24071407\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.859042638,9.769015283,10.6489835,11.48873305,12.28220461,13.0264691,13.72085487\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.168651988,9.802840023,10.45490141,11.11337564,11.76800587,12.41030608,13.03371026\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.027603668,9.688655584,10.35647941,11.02315179,11.68104888,12.32358795,12.94553688\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.090355671,9.729709031,10.38786273,11.05321851,11.71519151,12.36494414,12.99561412\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.916472559,9.570446467,10.23349838,10.89729241,11.55393809,12.19662769,12.81991026\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.005758519,9.905905563,10.77572832,11.60532756,12.38891091,13.12375326,13.80932285\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,7.936453993,8.70694431,9.462615821,10.20244226,10.92405452,11.62446834,12.30070536\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.482119227,10.23927232,10.97616134,11.68887615,12.37390289,13.028547,13.6510408\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,7.722032058,8.514882,9.290788144,10.04813687,10.7845742,11.4974102,12.18405176\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.970026999,9.882149636,10.76182627,11.59962577,12.39004885,13.13056279,13.8207762\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.132921607,9.768322991,10.42161399,11.08153566,11.73784252,12.38198312,13.00730764\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.924458435,9.600267834,10.27956331,10.95530357,11.62045724,12.2688559,12.89557249\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.598464942,10.334655,11.05734369,11.7606614,12.43956055,13.09022478,13.71010067\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.514452267,10.27092813,11.00974101,11.72570345,12.41444156,13.07272918,13.69849928\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,7.838228153,8.616093931,9.379753369,10.12718015,10.85557856,11.56185905,12.24309589\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.858371891,9.768823697,10.64915906,11.48918456,12.28285918,13.02726928,13.72175583\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.171798504,9.805206284,10.45659547,11.11449725,11.76864652,12.41054812,13.03362638\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.031189341,9.691585197,10.35882177,11.02497243,11.68241168,12.32455426,12.9461642\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.86291062,11.69171153,12.50173529,13.28159422,14.02311488,14.72121671,15.37341212\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.85343528,11.68362657,12.49473569,13.27547059,14.01771361,14.71641991,15.36912657\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.789485661,9.495756786,10.19754664,10.89215115,11.57530913,12.24235009,12.88894747\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.94438152,11.67598957,12.40149881,13.11146728,13.79802167,14.4552865,15.07934685\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.98283582,11.67392651,12.36404329,13.04386663,13.70541323,14.34249539,14.95074689\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.137580087,9.813228916,10.4898939,11.16405873,11.83047974,12.48357121,13.11825282\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,11.07530533,11.79716212,12.51389489,13.21557036,13.89415385,14.54376423,15.16053721\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.57002184,11.28471487,11.99616724,12.69608885,13.37694285,14.03267223,14.65889361\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.076222664,9.752887683,10.4299737,11.10406671,11.77013868,12.4228153,13.05717737\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,11.14118344,11.84983123,12.55473147,13.24597709,13.91551553,14.55740055,15.167667\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.67741159,11.3905818,12.09952304,12.79600521,13.47268761,14.1237473,14.74502066\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,8.78861686,9.495092327,10.19702898,10.89173919,11.57497368,12.24207048,12.88870905\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.94658755,11.67796945,12.40325835,13.11301967,13.79938423,14.45647826,15.08038697\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.98212129,11.67357305,12.36397607,13.04402632,13.70575168,14.34297308,14.9513313\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.131350287,9.807506622,10.48455795,11.15902939,11.82570581,12.47902023,13.11390411\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,11.07440247,11.79625074,12.51294829,13.21458282,13.8931307,14.54271569,15.15947484\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.56992568,11.28435655,11.99558535,12.69532302,13.37603129,14.03164985,14.65779098\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,9.067455222,9.745091435,10.42300848,11.09781919,11.7645153,12.41773754,13.05257852\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,11.13711921,11.84612187,12.55130908,13.24279187,13.91253118,14.55459057,15.16501181\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,10.68125674,11.39374237,12.10211327,12.79811785,13.47440013,14.12512519,14.74611942\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,14.42047061,15.33503088,16.15769421,16.89621383,17.55830699,18.15147365,18.68284324\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,15.42821995,16.12984489,16.7710917,17.35789326,17.89497606,18.38636398,18.83568286\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,14.45203816,15.38793727,16.22949427,16.98340359,17.65720299,18.25867365,18.79542377\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,14.7307816,15.65689352,16.48677022,17.2279345,17.88853333,18.47678488,19.00059965\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,14.25729356,15.19038282,16.02904463,16.78137859,17.45541415,18.05892671,18.59928415\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,15.45515947,16.1531415,16.7913426,17.3756036,17.91056191,18.40016462,18.84797438\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,14.33939539,15.28911094,16.14233859,16.90615938,17.58841517,18.19713274,18.74012086\n\"linker [O]S(=O)(=O)[O], n1cnn(c1)Cc1cc(cc(c1)Cn1ncnc1)Cn1ncnc1, nodes [Cd], topology \",,,14.67839185,15.6093911,16.44362143,17.18867459,17.85274851,18.44410478,18.97069329\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,20.38082034,20.53979949,20.66394425,20.76262879,20.84229989,20.90750183,20.96150811\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,19.92144512,20.09720231,20.23579846,20.3468533,20.43710189,20.51136395,20.57315599\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,19.16179312,19.33193468,19.46581391,19.57288331,19.65974608,19.73111627,19.79042521\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,20.13177358,20.2952791,20.42378509,20.5264712,20.60972795,20.67810585,20.73491067\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,18.09661396,18.76694112,19.32517916,19.79227052,20.18529662,20.51800462,20.80139363\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,12.75472189,13.24378285,13.64469667,13.97562196,14.25085045,14.48152991,14.6763433\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,10.09057143,10.52785137,10.88772413,11.1856666,11.43404664,11.6426133,11.81901838\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.66521481,17.2609844,17.75479749,18.16616033,18.51091123,18.80171309,19.04862697\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.762581686,4.294089474,4.838474186,5.388914785,5.938894599,6.482694977,7.015670791\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.119571725,3.51091506,3.946695199,4.41875321,4.917735414,5.434396168,5.960436826\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.188841598,3.661956804,4.171483705,4.707583384,5.260219995,5.820305513,6.380280908\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.92406121,3.381504386,3.879172736,4.407024832,4.954898384,5.513546173,6.075187051\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.722579198,4.22809196,4.76353925,5.317886312,5.880661787,6.442873777,6.997399261\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.372554333,3.887704938,4.434775884,5.002182366,5.579227089,6.156870484,6.728026157\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.59541084,4.074936785,4.588300113,5.125062715,5.674942944,6.228836241,6.779313762\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.013563848,2.404901597,2.842341217,3.316795629,3.818170127,4.336687643,4.863713744\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,4.023854816,4.558268244,5.094024185,5.625768074,6.148422243,6.657606396,7.149821286\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,4.34378962,4.843074182,5.35159442,5.864682827,6.377113049,6.883779182,7.38015083\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.801634847,3.214134238,3.672251371,4.165947726,4.684518639,5.217893201,5.757381831\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.428065417,2.886247294,3.383815781,3.909603011,4.452724305,5.003531986,5.554094599\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.910505949,3.336853746,3.803315786,4.302158403,4.824668097,5.362353238,5.907678576\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.495896041,3.972776326,4.485704338,5.023466668,5.575260486,6.131689436,6.685204034\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.577221914,2.98879847,3.443849926,3.935032737,4.453842118,4.991833812,5.541370594\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.110618181,2.538692596,3.021194783,3.548310783,4.109516674,4.694803692,5.295304894\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.558984579,2.973732239,3.436144001,3.936955264,4.466135702,5.014134678,5.572583898\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.033306559,3.475945536,3.948751612,4.445309253,4.958510859,5.48145788,6.008039112\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.82671982,4.345628473,4.871778806,5.399653386,5.923764949,6.439108176,6.941439046\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.074256555,2.481381377,2.9318367,3.416592392,3.926001702,4.450898381,4.983267168\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.741067587,3.216962788,3.726488146,4.258641281,4.803009928,5.350561603,5.894012551\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.088976413,2.538342679,3.025339418,3.539139649,4.06913363,4.605883374,5.141617913\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.981153492,3.445345281,3.948610679,4.479521129,5.027018396,5.581377395,6.134667208\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.997740507,3.43939951,3.922790445,4.43700901,4.971229247,5.515708675,6.062319357\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.067370458,3.550742427,4.071507767,4.618300517,5.180201493,5.747696223,6.313100986\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.767005124,3.207815593,3.692846736,4.212039776,4.754844253,5.311489695,5.873658499\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.347860851,3.798243132,4.269324372,4.754432719,5.246271801,5.737911849,6.223333706\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.274857849,3.714991834,4.170754397,4.636387982,5.105481252,5.57193588,6.030481786\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.282272501,2.678939597,3.118427608,3.592076992,4.090338212,4.603987212,5.124879145\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.072283294,2.516361556,2.999830776,3.512445691,4.043992352,4.585251934,5.128516276\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.228103366,2.717099959,3.239129923,3.782272331,4.335570772,4.889780015,5.437655572\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.225216103,2.687890759,3.185054625,3.706456007,4.241993994,4.782663561,5.321054979\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.395145244,3.97145469,4.563833341,5.159655601,5.748798391,6.323696868,6.879144023\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.680175801,3.163578984,3.679979182,4.217584608,4.76542407,5.314152338,5.856384211\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.212485291,2.640816733,3.110510985,3.610352545,4.129084559,4.656571586,5.18439574\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,4.700003235,5.260748275,5.812588879,6.352116765,6.876002833,7.381369392,7.865973245\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,4.10846722,4.60984012,5.124779618,5.647233285,6.171043194,6.690634421,7.201405016\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.877278326,3.335985342,3.836800349,4.367394039,4.915978584,5.472297234,6.028057313\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.175712112,2.607223198,3.080617892,3.585943608,4.113045897,4.652598541,5.196680236\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.472327411,4.019815538,4.595188768,5.185586164,5.779836434,6.368993838,6.94641195\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.7539306,4.240570782,4.758964126,5.298074106,5.847361612,6.397705329,6.941814351\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.885054625,3.356682354,3.868052397,4.40836984,4.966900512,5.534063421,6.101955938\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.168169541,2.584515406,3.053703219,3.567315658,4.115811345,4.689787453,5.280684965\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.590713515,2.990828373,3.437951279,3.92359812,4.438094855,4.971935616,5.51661684\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,4.433280208,5.058968418,5.678336146,6.284265347,6.871396039,7.435849654,7.974996465\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,4.146811677,4.709934186,5.27762192,5.843410663,6.401462165,6.946815904,7.4755209\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.241669876,3.646953807,4.095391912,4.578165167,5.085593558,5.60836394,6.138285127\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.725172153,4.291976703,4.882833899,5.485077811,6.087878588,6.682733698,7.263481143\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.813052827,3.238123685,3.704060608,4.202704771,4.725069375,5.26247469,5.807250784\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.425756911,3.916524685,4.442064589,4.991452087,5.554125561,6.120896409,6.684389915\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.860641432,3.28154028,3.743071755,4.237515354,4.756097933,5.290213859,5.83219035\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.504656766,3.992801243,4.515941578,5.062952067,5.623161387,6.187312473,6.747981827\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.282824731,2.713259783,3.183943003,3.684583528,4.204625021,4.73437881,5.265658406\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.836990886,4.34686283,4.864053416,5.38257903,5.896541707,6.400714544,6.890815511\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.03792557,3.456223242,3.895912787,4.351357088,4.815831576,5.282633991,5.745744399\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.174581384,2.571097591,3.01186024,3.487897697,3.989402781,4.50696253,5.032305684\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.150362793,2.620438173,3.126771297,3.657916035,4.203005277,4.752589198,5.299027984\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.084148166,2.51127956,2.977485383,3.47343751,3.989262594,4.515697442,5.044783487\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.381044798,2.878456051,3.407086646,3.955067289,4.511492625,5.06717703,5.614949554\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.224971601,2.586131927,2.992441991,3.438290624,3.916250349,4.418346047,4.936956597\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.681817669,3.150922867,3.657466953,4.189805677,4.736833867,5.288934312,5.838395647\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,1.744166475,2.089580169,2.483024719,2.917456249,3.383996691,3.873393669,4.377024967\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.683078888,4.185948147,4.70034181,5.22056512,5.740819946,6.255887044,6.76149227\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.667449145,4.189209381,4.721725065,5.258389144,5.792780091,6.319160471,6.832748729\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.008467479,2.427922017,2.889656041,3.383925043,3.900658837,4.430494931,4.965387638\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.618968871,3.080772011,3.577943054,4.099938541,4.636539287,5.178704294,5.719008847\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.068601484,2.508891141,2.987826891,3.495109643,4.020410313,4.554377554,5.089191383\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.907031416,3.383885787,3.89976693,4.442219517,4.999652365,5.562175161,6.121929848\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.908747936,3.336959319,3.807162974,4.309500249,4.833911301,5.371142793,5.913315872\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,3.019431478,3.515939942,4.050739079,4.611125105,5.185431617,5.763841308,6.338658568\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,2.638626488,3.021959823,3.451925416,3.921402115,4.421534762,4.94322293,5.478081415\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,4.03838328,4.525036706,5.017394717,5.511063204,6.001118502,6.482861126,6.952240528\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,12.53053862,12.91734214,13.23245031,13.49393426,13.71565606,13.90824205,14.07979361\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,15.52922605,16.15866759,16.67206459,17.09850897,17.46005595,17.77329144,18.05057856\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.28249936,14.9382964,15.48194897,15.94015804,16.33372269,16.67852452,16.9864852\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.79702619,15.37538006,15.84452759,16.23281913,16.56143368,16.84613358,17.0985736\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.402717833,9.695264388,9.932675503,10.12852319,10.29328379,10.43510619,10.56034695\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,15.15690047,15.7340013,16.20119292,16.58707171,16.91296637,17.19473966,17.44412297\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.1104852,14.87239339,15.50631529,16.04139775,16.50071456,16.90207045,17.25894627\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,13.17922709,14.02129834,14.7410283,15.36201681,15.90440214,16.38449037,16.81504717\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.00405404,14.57778665,15.0448996,15.43253809,15.76118424,16.04619508,16.29899134\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.57069877,15.25069021,15.81185596,16.2824732,16.68449712,17.03468732,17.34565456\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.36905467,15.11424175,15.73450021,16.25792987,16.70692125,17.09887957,17.44708353\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,15.23530397,15.8715505,16.39553629,16.83376924,17.20685273,17.53063894,17.81719732\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.59253071,15.31082531,15.9043237,16.40208858,16.82690524,17.19630031,17.52355237\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,15.17565611,15.82743806,16.35914936,16.80068878,17.17477102,17.4985034,17.78465626\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,13.34036081,14.17682449,14.8815682,15.48358788,16.00599699,16.4665973,16.87879057\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,14.79036393,15.44564196,15.98724918,16.44235197,16.83206695,17.17250053,17.47574299\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,10.25930835,10.85042224,11.45553066,12.06523174,12.6700869,13.26198708,13.83466185\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.851802229,10.49084983,11.13013756,11.76320486,12.38304302,12.98351013,13.55990458\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.253991913,9.836871317,10.43137108,11.02925564,11.62204596,12.20232068,12.76424935\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.838543983,9.480354595,10.12458577,10.76351265,11.3894478,11.99587995,12.57790603\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.120366029,9.718466537,10.32501214,10.93230355,11.53228673,12.11789036,12.68358061\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.544853087,10.14701576,10.75813284,11.37031451,11.97530817,12.56586701,13.1363159\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.178994763,8.784433646,9.40528415,10.02988627,10.64756243,11.24965522,11.8297805\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,10.1747242,10.77956079,11.39405791,12.00840038,12.61337589,13.2014517,13.7670731\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,7.424998416,8.005709815,8.601769207,9.202964337,9.799509686,10.38319062,10.94774611\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.207540519,9.831847296,10.45963603,11.08338959,11.69549978,12.28947328,12.86038898\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.270533825,8.897500553,9.532139462,10.16494434,10.78698137,11.39089282,11.97121586\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.429861591,9.017728934,9.613324276,10.21010037,10.80080789,11.37885578,11.93892853\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.203821858,9.784892171,10.36455462,10.94157139,11.51220239,12.07200212,12.61682057\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.399418494,9.978759569,10.56896846,11.16291769,11.75257268,12.33063614,12.89125415\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.265291238,8.863421491,9.47291454,10.08318422,10.68457094,11.26930809,11.83173703\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.98731108,9.602490993,10.22729974,10.85079361,11.46320384,12.05679712,12.62603297\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,7.435174116,8.058092149,8.690881822,9.322367329,9.942676804,10.54401368,11.12078779\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.881245187,9.49909876,10.12429799,10.74704219,11.35835588,11.95100031,12.51970981\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.128549735,8.728078433,9.3402164,9.954030701,10.55966682,11.1491955,11.71680208\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.678627673,10.2838489,10.89587298,11.5068271,12.10860734,12.6942314,13.25835379\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.906708356,10.49269014,11.08653856,11.68183858,12.27115012,12.84764868,13.40584375\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.708737732,9.308971296,9.920309989,10.53277097,11.13694208,11.72508396,12.29144735\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,7.143368246,7.733373277,8.337122292,8.944070877,9.544402284,10.1300407,10.69494642\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,6.550881636,7.147067211,7.756818168,8.36975595,8.97614961,9.567917088,10.13895355\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,6.239524865,6.84706101,7.468197734,8.091743536,8.707513793,9.307235736,9.884786853\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,8.146505539,8.731506039,9.329717149,9.931577148,10.5279121,11.11097069,11.67480066\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,7.047501935,7.629615073,8.227289824,8.830778035,9.43043687,10.01798138,10.58697078\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,7.396751086,8.000460883,8.619287399,9.242596783,9.860320421,10.46405464,11.0474181\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.001495864,9.297398468,9.54089943,9.744639454,9.918592554,10.07056408,10.20659416\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,17.25302796,17.63874394,17.95243879,18.21335283,18.435792,18.63035539,18.80482838\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.4740846,16.96042081,17.35825136,17.69050936,17.97428346,18.22221844,18.44358218\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,15.45818016,15.73348467,15.95895891,16.14833593,16.31196919,16.45758635,16.59086158\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,9.780445199,10.06861817,10.30189233,10.49371194,10.65435473,10.79174501,10.91202062\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,13.80873224,14.03648631,14.22269068,14.37936486,14.51551352,14.63782136,14.75116214\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.74720505,17.2896162,17.73519986,18.1082987,18.42726267,18.7057682,18.95389298\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,15.69262132,16.36242436,16.92782854,17.41105775,17.8299742,18.19853482,18.52742475\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,12.28241776,12.49807725,12.67354768,12.82102152,12.94947814,13.06548482,13.17375934\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.95613399,17.43147254,17.81966236,18.14334412,18.41942313,18.66043732,18.87559781\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.82762601,17.39161305,17.85764347,18.24902059,18.58370483,18.87536409,19.13427536\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,15.81748783,16.19119159,16.50214884,16.76519456,16.99202147,17.19172694,17.37127825\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.94327169,17.45049598,17.86718554,18.21569959,18.51306753,18.77213491,19.00248835\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,17.93230839,18.34806998,18.68571228,18.96595115,19.20416362,19.41173551,19.59703762\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.27862501,16.89484011,17.40273414,17.83025245,18.19797432,18.52086981,18.80971319\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,16.94472068,17.39753832,17.7668438,18.07480539,18.33784579,18.56805459,18.77424534\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,13.70396411,14.41112624,15.05363017,15.640767,16.17899288,16.67312578,17.12705896\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,12.75027018,13.48543637,14.15134891,14.75652232,15.30752104,15.80970009,16.26765087\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,13.22234297,13.98041702,14.6709279,15.30046004,15.87457428,16.39817725,16.87573415\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,12.80275894,13.52383823,14.18604387,14.79527873,15.35611829,15.87237988,16.34746364\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,13.22250471,13.97733598,14.66287907,15.286908,15.85562636,16.37424529,16.84733253\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,11.49188022,12.29252781,13.01497734,13.66843584,14.2604114,14.79723971,15.28443446\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,11.4504011,12.28079256,13.02743983,13.70106884,14.31021378,14.86190282,15.36212425\n\"linker NCCCCCCCN, [C]#N, nodes [Cd], [Ni], topology pcu\",,,13.31300375,14.0222222,14.6683639,15.25902181,15.7998381,16.29533576,16.74939997\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,20.02809734,20.50299562,20.88233766,21.18934476,21.44080777,21.64904363,21.82321448\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,19.97385055,20.45080825,20.83183001,21.14021911,21.39282912,21.60202507,21.77700605\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,18.0697329,18.80380072,19.40468656,19.90065841,20.31346522,20.65985657,20.95278699\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,18.08253692,18.8147507,19.414188,19.90900445,20.32087387,20.66649386,20.95878179\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.31966449,3.965705614,4.63574758,5.312861204,5.983612688,6.638171719,7.269944623\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.316698677,3.962571169,4.632531298,5.309632396,5.980423164,6.635058054,7.266931106\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.320249737,3.966991477,4.637611648,5.315194063,5.986319544,6.641172037,7.2731708\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.316945184,3.963534254,4.634068837,5.311619897,5.982755189,6.63764711,7.269705488\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.321994587,3.968791024,4.639449663,5.317052624,5.988180704,6.643019026,7.274988782\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.316754368,3.963410078,4.63400833,5.311615752,5.982797656,6.637725484,7.269809157\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.320965759,3.9670894,4.637155342,5.314251827,5.984959186,6.639457781,7.271161594\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.319438663,3.965420566,4.63539925,5.312451978,5.983148577,6.637660439,7.269394349\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.59676552,4.277731916,4.976014199,5.674438954,6.359911414,7.023276978,7.658768423\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.626541291,4.310602088,5.011054584,5.710807316,6.396896214,7.060308032,7.695407427\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.628222785,4.31278885,5.01368373,5.713803227,6.400179979,7.06380409,7.699047525\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,3.596474728,4.277376043,4.975593675,5.67395961,6.359382106,7.022707839,7.658169671\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.738096167,7.555834965,8.365503709,9.160898874,9.936932374,10.68935719,11.41472071\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.796683033,8.593728125,9.375223844,10.13861543,10.88080138,11.59860011,12.28915232\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.354883295,10.12191913,10.86828813,11.58980975,12.2828758,12.9447846,13.57380009\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.735257641,7.552608638,8.362168202,9.157621806,9.933810432,10.68644243,11.41203747\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.788969462,8.586521802,9.368504039,10.13235702,10.87497715,11.59318214,12.28411285\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.354686708,10.12178101,10.86817352,11.58969872,12.2827571,12.94465186,13.57364963\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.755285811,7.581263222,8.398515073,9.200499238,9.981954424,10.73859501,11.46702404\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.773215396,8.571907685,9.355102826,10.12015419,10.86390462,11.58314201,12.27499364\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.35943881,10.12581479,10.87129741,11.59177445,12.28370069,12.94443072,13.57227534\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.753351797,7.57929984,8.396579527,9.198623755,9.9801537,10.73687236,11.46537597\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.771559658,8.569895824,9.352764844,10.11751885,10.8609994,11.57999294,12.27162504\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.350162246,10.1165098,10.86200352,11.58251244,12.27447958,12.93525236,13.56313746\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.75603178,7.582129478,8.39939175,9.201294737,9.982602158,10.73905421,11.4672768\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.779567248,8.577886404,9.360653346,10.12526061,10.8685763,11.58740355,12.27887778\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.357827327,10.12412854,10.86960983,11.59012503,12.2821086,12.94290327,13.57081322\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.745847086,7.571872286,8.389095591,9.191001183,9.972349229,10.72887195,11.45718657\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.763269246,8.561885671,9.344958496,10.10986952,10.85347876,11.5725837,12.26431628\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.344194605,10.1105344,10.85602924,11.5765455,12.26852454,12.92931256,13.55721525\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.736060987,7.55320739,8.362248685,9.157041246,9.932536017,10.68450747,11.40951122\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.794119943,8.591620471,9.373549964,10.13734718,10.87990528,11.5980392,12.28888812\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.352680202,10.11993303,10.86647521,11.58814372,12.28134023,12.94336822,13.57249409\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,6.728308936,7.545123669,8.354102465,9.148986382,9.924657035,10.67684791,11.4020907\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.783203039,8.581336261,9.363855368,10.12820004,10.87126573,11.58987014,12.28115525\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.353991922,10.12132521,10.86791748,11.58960993,12.28280713,12.94481517,13.57390321\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.384430638,10.1690864,10.93104796,11.66572774,12.36945392,13.03965788,13.67483625\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.482553256,8.306478655,9.110211315,9.891481197,10.64799173,11.37744054,12.07773326\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.385529042,10.16807195,10.92846035,11.66210649,12.36526066,13.03525074,13.67047237\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.463534726,8.281154427,9.079771556,9.856883704,10.61004461,11.33684652,12.03511112\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.381958631,10.16500482,10.92582522,11.65983973,12.36330621,13.03355988,13.66900315\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.462961371,8.280645973,9.07931689,9.856473436,10.60967108,11.33650355,12.03479368\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,9.383151135,10.16822922,10.9305457,11.66552792,12.36951225,13.03993507,13.67529677\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,7.483573974,8.307454607,9.111113434,9.892294524,10.64871094,11.37806649,12.07827045\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.06535749,14.91787815,15.6824981,16.37026333,16.9904891,17.55106683,18.05873454\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.68070876,15.45162598,16.14245779,16.76422773,17.32600948,17.83526913,18.29819317\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.17086595,15.0057398,15.7556359,16.43104557,17.04084264,17.59256673,18.09267474\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.72578546,15.49416517,16.18260919,16.80216906,17.36192452,17.86933641,18.33058049\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.90155462,15.63819083,16.2969233,16.88935241,17.42479822,17.91075666,18.35330416\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,13.68219113,14.56085178,15.35159403,16.06403379,16.70669646,17.28711759,17.81196235\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.97407189,15.70698505,16.36237774,16.95183679,17.48465337,17.9682889,18.40878472\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,13.73389992,14.61484301,15.40724811,16.12092615,16.76453203,17.34568765,17.87111639\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.87707585,15.61511779,16.27464412,16.86747606,17.40308055,17.88905169,18.33153103\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,13.68609109,14.56717397,15.35978651,16.07371374,16.71758947,17.29902,17.82471799\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.87760819,15.61878937,16.28125438,16.87677865,17.41481958,17.90298044,18.3474208\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,13.69145959,14.57295762,15.36614946,16.08070707,16.725199,17.3071971,17.83339864\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.08006819,14.93185981,15.69559265,16.38241927,17.00172139,17.5614292,18.06830094\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.63986722,15.41839819,16.11569944,16.74299218,17.30950963,17.82284779,18.28929945\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.14421227,14.98478827,15.73937886,16.41868482,17.03174738,17.58623739,18.08871336\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,14.69057483,15.45899822,16.14753583,16.76721413,17.32709943,17.83464547,18.29602414\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,16.55533344,17.43376187,18.16162684,18.76777369,19.27562486,19.70389738,20.06745322\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,16.33498645,17.20683145,17.92933738,18.53109006,19.03530896,19.46055402,19.82156586\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,16.67132019,17.54975693,18.27677584,18.88167946,19.38813951,19.81500635,20.17721057\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ni], [O], topology \",,,16.35814888,17.23457242,17.96046862,18.56477613,19.07095388,19.49772572,19.85994596\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,16.76764182,17.61719437,18.33259229,18.93891195,19.45593696,19.89939023,20.2818543\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,16.77069014,17.61984891,18.33491597,18.94095724,19.45774721,19.90100112,20.28329521\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,3.264593549,3.940593321,4.63480852,5.330924811,6.016273025,6.681785642,7.321558948\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,3.265062842,3.94100639,4.635169621,5.331239509,6.01654713,6.682024658,7.321767832\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,3.264593255,3.940592496,4.634808383,5.330926118,6.01627616,6.681790713,7.321565882\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,3.265027483,3.940965403,4.635124105,5.331190619,6.016495947,6.681972133,7.321714759\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.747822703,8.54424982,9.327837453,10.09529351,10.84257971,11.56568868,12.26115004\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.363525386,8.24858884,9.11798208,9.964620904,10.7824876,11.56682746,12.31422501\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,9.176216368,10.02932311,10.84139561,11.61163256,12.3397594,13.0259861,13.67097374\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,6.599661664,7.397361711,8.18621136,8.960854894,9.716941768,10.45080312,11.15938358\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.714639183,8.504501834,9.273028233,10.0184037,10.7392899,11.43436737,12.10232089\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.748945297,8.545230669,9.328703532,10.09606747,10.84327966,11.56632862,12.26174068\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.365171932,8.250026159,9.119252992,9.965758818,10.78351813,11.56777005,12.31509437\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,9.177830806,10.03065317,10.84248172,11.61251318,12.34046886,13.02655403,13.67142517\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,6.600306432,7.397950099,8.186775229,8.961414997,9.717510302,10.45138606,11.15998263\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.717524548,8.506641807,9.274595245,10.01952919,10.74007529,11.43489133,12.1026445\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.74818314,8.544561907,9.328109674,10.0955326,10.84279108,11.5658767,12.26131828\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.363752257,8.248766304,9.118123198,9.964734955,10.78258124,11.56690551,12.31429098\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,9.17617753,10.02927993,10.84134827,11.61158168,12.33970581,13.02593067,13.67091729\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,6.599663952,7.397363224,8.186211225,8.960852942,9.716938192,10.45079826,11.15937782\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.715480887,8.505156733,9.273544999,10.01881702,10.73962495,11.43464271,12.10255028\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.748617239,8.544925819,9.328417008,10.09579628,10.84302196,11.5660833,12.261507\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.364969485,8.249856757,9.119105712,9.965626377,10.78339573,11.56765459,12.3149839\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,9.17789277,10.03070662,10.8425297,11.61255798,12.34051213,13.02659686,13.67146821\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,6.600294705,7.397920602,8.186731937,8.961360981,9.717448053,10.45131765,11.15990979\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,7.716923521,8.506174319,9.274226171,10.01923363,10.73983525,11.43469362,12.10247934\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,14.15973576,14.96474054,15.68421434,16.33033922,16.91303954,17.44042083,17.91916072\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,13.8420056,14.68407971,15.43533601,16.10869262,16.71476311,17.262261,17.75838333\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,17.46499372,17.92987669,18.34256248,18.71519224,19.05583248,19.36986479,19.66093743\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,16.95867864,17.4747189,17.93370207,18.34773868,18.72517067,19.07177575,19.39163319\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,14.16722324,14.9712077,15.68984736,16.33528462,16.91741323,17.44431509,17.92264955\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,13.84895189,14.68992116,15.44031652,16.11299377,16.71852106,17.26557876,17.76133962\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,17.5184003,17.97570885,18.38236625,18.75011697,19.08674922,19.39744521,19.68570782\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,16.98873966,17.5007134,17.95639296,18.36771201,18.74288313,19.08758794,19.40583325\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,14.16035661,14.96529295,15.68470774,16.33078183,16.91343843,17.44078196,17.91948914\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,13.83928266,14.68164724,15.43315554,16.10673075,16.71299123,17.26065473,17.75692192\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,17.47551744,17.9388889,18.35037815,18.72204358,19.06189428,19.37527102,19.66579255\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,16.97040998,17.48472763,17.94233695,18.35526159,18.73178171,19.07763018,19.39685318\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,14.16659706,14.97063408,15.68932497,16.33481025,16.91698285,17.44392446,17.92229457\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,13.85188934,14.69253001,15.44264234,16.11507542,16.7203915,17.26726588,17.76286707\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,17.51135776,17.9696759,18.37713078,18.7455235,19.08268124,19.39381368,19.68244343\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,16.98048368,17.49367306,17.95032334,18.36242853,18.7382444,19.08348402,19.40217755\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,15.22372957,16.17767697,17.0100123,17.73694227,18.37265531,18.92958112,19.41854898\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Al], [O], topology rna\",,,15.2228769,16.17692009,17.00933817,17.73633958,18.37211436,18.92909367,19.41810806\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,19.91678198,20.02866611,20.11545802,20.18406148,20.23918086,20.28410442,20.32118297\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,19.91680235,20.02868308,20.11547237,20.18407377,20.23919149,20.28411372,20.32119116\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.508442079,4.164772904,4.840618525,5.5198876,6.189938392,6.841641885,7.468997964\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.470566122,4.133771269,4.816300671,5.501722755,6.177208229,6.833552221,7.464752618\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.540388941,4.18240976,4.844215489,5.510430792,6.168834861,6.810471304,7.429333323\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.269014112,3.929816867,4.613309254,5.302316471,5.983450953,6.647095069,7.286943144\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.497876759,4.163769187,4.849113102,5.537252998,6.215236385,6.873820572,7.507026185\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.2080989,3.858836714,4.536454389,5.22306591,5.904340677,6.56974672,7.212206775\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.508596338,4.164939064,4.840793308,5.520067883,6.190121411,6.841825322,7.469179961\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.470381498,4.133568645,4.816085043,5.501498764,6.176979902,6.83332289,7.464524942\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.539907393,4.181895929,4.843679868,5.509882724,6.168282241,6.80992055,7.428789478\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.26862505,3.929388181,4.612852847,5.301843034,5.982969475,6.646612765,7.286465586\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.498047541,4.163939292,4.849279771,5.537414182,6.215390659,6.873967004,7.507164209\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,3.208233968,3.858984175,4.536610368,5.223226894,5.904503647,6.569909173,7.212366676\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,8.396873178,9.225603102,10.03920664,10.83235397,11.59969667,12.33664715,13.03974321\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.586862596,10.35381334,11.09204633,11.79999474,12.47628225,13.119878,13.73019266\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.534228556,10.30825988,11.05174613,11.76358526,12.44278501,13.08861058,13.70068986\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.643929684,10.40374884,11.13706411,11.84162031,12.51552847,13.15738893,13.76635522\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.630685155,10.40095078,11.13985002,11.84657762,12.52041809,13.16086545,13.76772068\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,8.265858536,9.110620156,9.940256082,10.74875795,11.53035185,12.28021915,12.99480812\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.566139168,10.32820353,11.06190751,11.76566973,12.43818264,13.07849855,13.68608926\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,8.284369385,9.097695061,9.900227107,10.6863505,11.45016016,12.18641496,12.89101143\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.510373104,10.27804222,11.0142332,11.71865556,12.39086531,13.03046325,13.63725144\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,8.396863483,9.225589029,10.03918869,10.83233273,11.59967274,12.33662111,13.03971559\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.586866218,10.35381233,11.0920411,11.79998571,12.47626988,13.11986278,13.73017504\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.534211994,10.30824192,11.0517273,11.76356606,12.44276586,13.08859179,13.70067166\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.643971531,10.40378615,11.13709568,11.84164585,12.51554818,13.15740329,13.76636483\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.630693997,10.40094992,11.1398392,11.84655736,12.52038932,13.1608293,13.76767833\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,8.265866355,9.110622556,9.940253572,10.74875111,11.53034127,12.28020542,12.9947918\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.566172122,10.3282196,11.06190912,11.76565902,12.43816152,13.07846873,13.68605227\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,8.284379392,9.097706485,9.900238323,10.68636036,11.45016795,12.1864203,12.89101421\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,9.510360416,10.27803315,11.01422818,11.71865467,12.3908684,13.03046997,13.63726137\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,19.20180314,19.80012809,20.29131526,20.69868017,21.03971855,21.32770626,21.57283109\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,18.94193815,19.56419914,20.07719074,20.50418134,20.86277056,21.16640368,21.42545931\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,18.78621526,19.40626355,19.92188162,20.35422663,20.71961984,21.03072622,21.297448\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,19.20179127,19.80011543,20.29130237,20.69866741,21.03970615,21.32769435,21.57281972\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,18.9419395,19.56419865,20.07718902,20.50417882,20.86276753,21.16640034,21.42545581\n\"linker S=C1C=CC(=S)C=C1, [S]c1ccc(cc1)[S], nodes [Cd], topology pcu\",,,18.78621663,19.40626959,19.92189079,20.35423782,20.71963226,21.03073931,21.29746136\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,20.06960627,20.51167518,20.86264972,21.14582727,21.37757292,21.56961891,21.73053923\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,20.07723698,20.51926885,20.87005314,21.1529528,21.38437348,21.57607311,21.73664199\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.567373109,4.234880099,4.920366049,5.607162737,6.282509498,6.937391782,7.566026327\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.530162633,4.186290234,4.862686881,5.542646137,6.213210851,6.865102604,7.492260454\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.12919972,3.758992543,4.41890688,5.091154584,5.761335201,6.418709834,7.055904421\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.034751712,3.630433261,4.260082061,4.906986943,5.557004745,6.199132424,6.825446709\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.468367235,4.129932513,4.81347511,5.501256991,6.179620945,6.838877708,7.472767397\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.491798832,4.156503012,4.841890408,5.530465737,6.20882418,6.867499282,7.500411538\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.22801605,3.827107981,4.4554515,5.097376328,5.7397962,6.372626634,6.98867161\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.126238575,3.729151424,4.360929138,5.006027153,5.651464065,6.287225941,6.90615522\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.414614639,4.08082439,4.768878134,5.46086005,6.143013713,6.805602857,7.442354139\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.483139167,4.150129015,4.837796144,5.528516051,6.208818818,6.869220608,7.50365511\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.304887649,3.916699924,4.553872976,5.201263841,5.846427895,6.479905713,7.095048507\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.562357529,4.229757123,4.915256725,5.602160697,6.277681444,6.93278129,7.56165866\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.528717713,4.184573803,4.860781954,5.54062662,6.211136665,6.863019406,7.49020134\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.12490952,3.753031694,4.411362175,5.08219684,5.751181056,6.407591448,7.044048534\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.043748898,3.639277816,4.268686038,4.915289027,5.564965895,6.206731082,6.832674443\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.469267138,4.13050593,4.813789371,5.501368906,6.179577093,6.838715538,7.472516594\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.491311616,4.155741746,4.840952156,5.529426624,6.207740634,6.866411287,7.499346258\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.226903638,3.826086167,4.454499504,5.096482086,5.738952739,6.371829688,6.987918214\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.120141013,3.722188931,4.35324373,4.997774394,5.64279627,6.278282315,6.89705703\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.412551985,4.078537877,4.766446607,5.458353748,6.140489413,6.803103615,7.439911\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.483093774,4.149917506,4.83744817,5.528064712,6.208295174,6.868651614,7.503063214\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,3.301159819,3.913217356,4.550640595,5.198276759,5.843674264,6.477369386,7.092711096\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.310327108,8.159262093,8.991943177,9.804081781,10.59139658,11.35003102,12.07685855\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,6.975996583,7.85057336,8.718823322,9.570630006,10.39784498,11.1942719,11.95552796\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.581530567,8.39590168,9.199866485,9.988049424,10.75523774,11.49682878,12.20911148\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.582257895,10.34033477,11.07404687,11.78028863,12.45666616,13.10148398,13.71372258\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.867988301,10.61198521,11.32792301,12.01408622,12.66939118,13.29318058,13.88516712\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.769716081,10.49862453,11.20409568,11.88451959,12.53808537,13.16318127,13.75861929\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,6.707180999,7.518098349,8.32140141,9.109835455,9.877872033,10.621289,11.33692499\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,6.458272409,7.262002751,8.06135209,8.850064396,9.622718411,10.37460703,11.10178198\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.265936817,9.990042459,10.70164281,11.39598104,12.06867218,12.71608532,13.33550716\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.66517463,10.4036899,11.12210848,11.8166042,12.48401589,13.12198014,13.72894654\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.530685938,8.307311989,9.077690859,9.836417397,10.57837208,11.29895631,11.99431771\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.62822908,10.3713886,11.09310964,11.78992759,12.45897256,13.09810557,13.70594183\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.280136164,9.997364405,10.70395248,11.39453827,12.06434785,12.70950674,13.32714807\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.180952668,9.913189634,10.63171154,11.33182152,12.00928885,12.6606675,13.28342103\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.635208753,10.37574339,11.09526607,11.79029993,12.45793629,13.09598622,13.70301265\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.561870485,8.333945374,9.099770411,9.854126283,10.5920234,11.30893996,12.00105714\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.680087649,10.42223084,11.14319008,11.83938384,12.50784748,13.1463742,13.75353712\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.279709749,10.00848833,10.72428752,11.42207921,12.0974016,12.7466622,13.36724278\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.330871879,8.178748086,9.010345374,9.82141747,10.60770551,11.3653641,12.09127143\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,6.97708785,7.850531271,8.717802899,9.568803556,10.39537853,11.19131418,11.95220648\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.588720041,8.402643144,9.206149679,9.993902307,10.76070099,11.50194384,12.21391571\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.577758052,10.3354817,11.06888603,11.77489376,12.45111864,13.09586099,13.70809124\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.85699673,10.60110146,11.317253,12.00371758,12.65938647,13.28357915,13.87598975\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.772434905,10.50076752,11.20583281,11.88598614,12.53938139,13.16437659,13.75976016\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,6.716787118,7.524789053,8.325489035,9.111650603,9.877742902,10.61952699,11.33381576\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,6.448905571,7.255286279,8.056655276,8.84691727,9.6207624,10.37356459,11.10143674\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.275479885,9.998335474,10.7089493,11.40250248,12.07456146,12.72145808,13.34045104\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.680641514,10.41791163,11.1351769,11.82861695,12.49506957,13.13216627,13.73834964\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.527570301,8.304555416,9.075254608,9.834263679,10.57646565,11.29726534,11.99281406\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.639616116,10.3814551,11.10198619,11.7977514,12.46587527,13.10420752,13.71134997\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.282770837,10.0001317,10.70676512,11.39733739,12.06709484,12.71217712,13.3297271\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.184826526,9.91676471,10.63497995,11.33479424,12.01198614,12.66311341,13.28564032\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.634154004,10.37442819,11.0936767,11.78845667,12.45587549,13.0937499,13.70064271\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,7.57300298,8.345065934,9.110754357,9.864890071,10.60251065,11.31911288,12.0108912\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.673067264,10.41526383,11.13630495,11.83262059,12.50124485,13.13996425,13.74734364\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,9.283861333,10.01312925,10.72923177,11.42719148,12.10258299,12.75184038,13.37236505\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,10.22576175,10.99322782,11.73458014,12.44856436,13.13320728,13.78656957,14.40715986\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,10.22036324,10.97280234,11.70027202,12.40208972,13.07652708,13.72166412,14.33588988\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,10.23688831,11.00291458,11.74317985,12.45633811,13.1403429,13.79319979,14.41337766\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,10.24081462,10.99248326,11.71936683,12.42070412,13.09470892,13.73942383,14.35321675\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,13.43838427,14.3474506,15.16338921,15.89823333,16.56162371,17.16155037,17.70482687\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,15.69777839,16.3371029,16.90271295,17.4083825,17.86451781,18.27902456,18.65795008\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,14.34839348,15.10103108,15.77809145,16.39172588,16.95076999,17.4618737,17.93024755\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,13.17963284,14.03976795,14.81602075,15.51955931,16.1592195,16.74217428,17.27439749\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,13.08523346,14.02644496,14.8719248,15.63346379,16.3207602,16.94199944,17.50424304\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,15.97185676,16.58755742,17.13160068,17.61782735,18.05653776,18.45546157,18.82045092\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,13.96673431,14.75724493,15.46694115,16.1088962,16.6926826,17.2255364,17.71313635\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,13.19805708,14.05548942,14.82909531,15.53024012,16.16782992,16.74904163,17.27982207\n\"linker [O-]C(=O)c1c(cccc1C(=O)[O-])Oc1cccc(c1C(=O)[O-])C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], topology \",,,12.00337435,13.07514521,14.04859756,14.9287845,15.72242568,16.43692348,17.07976786\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,20.31416493,20.81543349,21.21252926,21.53182728,21.79203686,22.00666322,22.18561976\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,17.88848094,18.29555533,18.61782308,18.87687608,19.08797418,19.26210481,19.40731926\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.581662211,4.19800226,4.83494723,5.478263628,6.116485882,6.74105902,7.346099357\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.712137607,4.389119197,5.080904453,5.771009418,6.447113439,7.100730202,7.726593473\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.696027882,4.383830552,5.085274031,5.783744224,6.466875625,7.126218405,7.756601681\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.327940552,3.947297334,4.589516836,5.23977687,5.886097606,6.519501466,7.133771852\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.88507015,4.527814696,5.179663421,5.828786013,6.465932857,7.084425148,7.679887128\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.648543695,4.262924895,4.89763575,5.538602487,6.1744432,6.796647304,7.399356366\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.818855134,4.495688542,5.183961273,5.868316114,6.537380772,7.183382206,7.801549085\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.804998011,4.485394247,5.179565431,5.871149873,6.547912214,7.201460458,7.826640156\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.404489467,4.022924399,4.661622907,5.306632638,5.946757115,6.573638229,7.181505767\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.85109514,4.508283777,5.174927766,5.838224936,6.488293077,7.118110721,7.723176939\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.624133572,4.239289606,4.874550104,5.515895207,6.151985189,6.774341989,7.377132021\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.807404583,4.484490395,5.172864786,5.857211162,6.526189301,7.172050908,7.790043367\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.813858209,4.494421767,5.188676772,5.880274846,6.556994903,7.210458263,7.835522011\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.401956158,4.020740217,4.659683598,5.304851726,5.945064904,6.571979993,7.179839611\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.853748613,4.510680614,5.177099071,5.840197272,6.4900861,7.119738143,7.724648398\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.567104464,4.183102449,4.819870483,5.463137554,6.10140616,6.726095265,7.331300529\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.706897437,4.384164065,5.076342335,5.766890726,6.443449753,7.097508889,7.723788134\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.661856149,4.349207792,5.050536975,5.749159934,6.432649428,7.092502758,7.723505049\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.31797822,3.937353813,4.579804907,5.230450972,5.877257043,6.51119993,7.126028498\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.866296881,4.505783454,5.154662442,5.801198647,6.4361918,7.052972303,7.647144321\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.184277446,3.778010692,4.401759906,5.03995102,5.67952819,6.310391907,6.925300013\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.616667721,4.289508705,4.977628385,5.664918236,6.339229476,6.992113081,7.61825689\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.307057232,3.970016043,4.657240222,5.350501821,6.035607543,6.702395582,7.344233777\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.028777411,3.611479117,4.22593018,4.85680861,5.491220746,6.119116687,6.73320154\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,1.956394477,2.478153875,3.056317052,3.673503093,4.313211663,4.961334088,5.606724192\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,1.999390473,2.527451936,3.111456369,3.733806069,4.377903502,5.029639716,5.677935438\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.649257784,4.314719618,4.999105747,5.685141454,6.359748748,7.013808534,7.641561333\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.53537999,4.146320532,4.779796557,5.421147904,6.05855602,6.683174012,7.288881048\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.333967255,3.920907103,4.536349174,5.165328243,5.79535262,6.416770675,7.022659893\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.679602953,4.347999504,5.034875374,5.722892221,6.398958681,7.053980012,7.682245022\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.29163122,3.895056831,4.523369237,5.161994801,5.79896357,6.425149803,7.034099271\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.481295929,4.139154265,4.817449978,5.499345715,6.171836011,6.825657038,7.454795586\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.46593602,4.132241211,4.81974799,5.510864007,6.192034059,6.853654162,7.489542831\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,2.851574056,3.420186432,4.02538206,4.651481095,5.284916878,5.914880143,6.533356913\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,2.017066273,2.549434395,3.136760258,3.761411274,4.406812969,5.058911202,5.706695233\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,2.110368987,2.659858103,3.262482663,3.900147024,4.55613785,5.216498471,5.87046349\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.327013609,3.982177217,4.662759133,5.350319638,6.030555362,6.693233041,7.331657777\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.410106341,4.006224294,4.629612897,5.264985349,5.899762972,6.524358584,7.132000469\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.35450559,3.94589367,4.564741743,5.196075481,5.827516436,6.44957439,7.055493422\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.600549285,4.270467224,4.959685625,5.650597212,6.329883132,6.98827503,7.619937613\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.292881079,3.895624733,4.523406172,5.161635754,5.798323052,6.424321526,7.033157922\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.487708519,4.145192496,4.823168495,5.504803602,6.177090224,6.830758966,7.459789642\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.461071152,4.127994871,4.816090505,5.507735288,6.189360071,6.851357994,7.487551337\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,2.851256034,3.419783713,4.024932015,4.651014705,5.284457527,5.914444164,6.53295483\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,2.015821342,2.547847359,3.134862754,3.759247418,4.404431423,5.056359825,5.70401793\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,2.108834685,2.657618972,3.259613239,3.896741415,4.552297547,5.212323226,5.866045464\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.33483946,3.98992813,4.670365178,5.35772493,6.037720477,6.700134088,7.338283978\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.410411782,4.006373317,4.629651225,5.264976213,5.899786923,6.524513051,7.132398152\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.356048834,3.947686029,4.566739355,5.198253599,5.829863519,6.452087255,7.058173667\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.607123041,4.277043658,4.966128303,5.65681393,6.335818743,6.993902602,7.625250227\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.166925601,3.760362275,4.383883906,5.021915929,5.661398408,6.292225339,6.907146767\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.624964829,4.297133928,4.984652493,5.671415032,6.345272411,6.997772423,7.623597702\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.293320863,3.956589477,4.644033572,5.337430738,6.022601138,6.68939868,7.331206013\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,2.993659356,3.576383634,4.191204572,4.822697946,5.457878008,6.086620973,6.701577326\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,1.950169657,2.471849557,3.049893767,3.666940308,4.306502945,4.954482546,5.599738769\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,1.995676191,2.524102468,3.108408259,3.73099798,4.375276662,5.027139146,5.675511183\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.640705297,4.306066527,4.990500005,5.676691089,6.351527908,7.005864612,7.633921525\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.525796629,4.135755682,4.768408172,5.409101553,6.046011003,6.670275229,7.275755085\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.335389122,3.922763471,4.538597386,5.167908735,5.79820184,6.419828132,7.025871533\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,3.67661581,4.345001776,5.031871376,5.71988998,6.395968844,7.051014365,7.679315209\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.693398831,10.43068647,11.15026832,11.8470376,12.51719765,13.1580899,13.76803616\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.05683417,10.79851392,11.51545961,12.20460855,12.86374239,13.49140806,14.08683229\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,8.229624743,8.986358586,9.731500696,10.46267646,11.17662058,11.86979956,12.53892495\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.887701775,10.65834195,11.39636179,12.10085375,12.77126864,13.40737945,14.00928445\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.551599068,10.31430009,11.05229405,11.76258514,12.44286174,13.09149295,13.7075063\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.22829232,10.98297167,11.70514102,12.39483634,13.05180873,13.67580382,14.26675445\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.684975762,10.4183431,11.13328263,11.82526903,12.49090392,13.12777319,13.73432489\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.09730383,10.83732435,11.55234355,12.23932747,12.89613798,13.52141227,14.11445687\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,8.226971343,8.985478165,9.731717581,10.46349813,11.17770163,11.87090587,12.53990308\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.996042731,10.75146567,11.47709693,12.17131304,12.8330757,13.46181853,14.05739793\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.648845921,10.40989616,11.14634676,11.85493034,12.53321879,13.17956396,13.79303148\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.13971294,10.90289129,11.6321381,12.32786004,12.99005115,13.61861426,14.21358665\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.454869086,10.19151131,10.90924973,11.60366762,12.27143984,12.91020413,13.51844701\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.966489772,10.7084208,11.42493935,12.11311083,12.7708708,13.39691216,13.99058392\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,8.199824916,8.959479793,9.70671403,10.4393634,11.15433407,11.84822462,12.51784424\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.01470398,10.76978651,11.49506469,12.18893318,12.85036126,13.47878518,14.07406178\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.596738725,10.35915009,11.0967123,11.80620584,12.48523925,13.13219347,13.74615784\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.15336897,10.91591786,11.64451365,12.33958447,13.00114012,13.62909556,14.22349695\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.674210981,10.41071641,11.12968298,11.82596462,12.49573235,13.13630165,13.74597426\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.09030439,10.8309277,11.54708747,12.23564794,12.89433628,13.52165829,14.11680997\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,8.243320488,8.997376573,9.740172875,10.46930177,11.18147222,11.87312558,12.54094746\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.879998358,10.64872748,11.38504899,12.08803719,12.75712563,13.39206997,13.99295133\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.55834584,10.3205689,11.05798422,11.76767175,12.44737059,13.09548036,13.71104411\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.21668236,10.96778284,11.68679205,12.37368889,13.02818275,13.64998507,14.23899834\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.418213536,10.13983355,10.84952361,11.54220739,12.21336788,12.85934311,13.47743055\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.793003096,10.53558438,11.25552033,11.94996257,12.61637735,13.25281387,13.85799302\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.799472429,8.577837493,9.346190569,10.10118203,10.838762,11.55483606,12.24575469\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.697254347,10.46683324,11.20836917,11.9203313,12.60113693,13.24950351,13.86462583\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.629977605,10.35979741,11.07566018,11.7726419,12.4463168,13.09312576,13.71050695\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.449157605,8.441144824,9.413768439,10.35242759,11.24716117,12.0919346,12.88380189\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.418941617,8.419446693,9.401033611,10.34843882,11.25127892,12.10329048,12.90143895\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.808602326,8.576753623,9.335997719,10.08296201,10.81358278,11.52373126,12.20970002\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.909533141,10.62258994,11.321922,12.00210923,12.65868342,13.28828653,13.88864353\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.49130316,10.19341507,10.89170249,11.57809788,12.24606223,12.89058903,13.50810323\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.568624559,10.25625521,10.94026426,11.61341725,12.26958322,12.90390234,13.51279149\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.92926842,10.64426848,11.34378481,12.02316131,12.6784627,13.30667245,13.90571592\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.459411938,10.19048681,10.90821853,11.60732085,12.2832779,12.93255486,13.55263879\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.769431419,10.50588349,11.22138113,11.91283264,12.57743221,13.21297389,13.81795901\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.769553192,8.554072327,9.328819348,10.09014654,10.8337699,11.55543395,12.25139492\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.814685247,10.57252564,11.30499022,12.00987868,12.68506367,13.32884981,13.9401322\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.541345673,10.27682201,10.99749828,11.69879777,12.37648656,13.02709783,13.64810594\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.414304979,8.41199818,9.389731211,10.33292286,11.23164377,12.07989765,12.87478083\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.368573709,8.362781446,9.34000476,10.28490284,11.18682777,12.03918959,12.83863566\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.86488458,8.627712894,9.382423196,10.12566676,10.85328699,11.56102097,12.24502641\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.874979241,10.59455551,11.29714327,11.97855632,12.63517398,13.26419747,13.86370698\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.519593065,10.21000376,10.897691,11.57475181,12.23465847,12.87233405,13.48409408\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.558015962,10.25146868,10.94133856,11.61998411,12.28102053,12.91945948,13.53168082\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.893329488,10.61924364,11.32777909,12.01454983,12.67584753,13.30885667,13.91168334\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.477344509,10.2069351,10.92345625,11.62157652,12.29674041,12.94537952,13.56495287\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.790171507,10.52634398,11.24170816,11.93313593,12.59779186,13.23344662,13.83858352\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.763120601,8.547893539,9.322919721,10.08453072,10.82842726,11.55034399,12.24653176\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.799596939,10.55729372,11.28958128,11.99426675,12.66922727,13.31277092,13.92379605\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.537641406,10.27285648,10.99319413,11.69411397,12.37140907,13.02163133,13.64226709\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.41700198,8.414757199,9.392374479,10.33531998,11.23370368,12.08156064,12.87601141\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.372915214,8.367059679,9.344262401,10.28915235,11.1910629,12.04339449,12.84279108\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.882419935,8.645247673,9.399958268,10.14319209,10.87078851,11.5784843,12.26243879\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.92794017,10.64633623,11.34783787,12.02823131,12.6838797,13.31197547,13.91059455\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.565199721,10.25535996,10.94287004,11.61981834,12.27966942,12.91733889,13.52913528\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.603084527,10.29838286,10.98985798,11.66991526,12.33220242,12.97175467,13.58496997\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.913613073,10.64004494,11.34911085,12.03640463,12.69820621,13.33169388,13.93497111\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.321007992,10.042463,10.75199042,11.44451657,12.11552683,12.76136086,13.37931692\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.805009608,10.54602189,11.26472947,11.95821647,12.62389102,13.25975475,13.86449067\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.785275194,8.564246934,9.333235677,10.08884779,10.82700166,11.543583,12.23493225\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.581123762,10.3513161,11.09350011,11.80610704,12.48752151,13.13643765,13.75203649\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.434960036,10.16491007,10.88086159,11.57790664,12.25162678,12.89846528,13.51586054\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.444977776,8.437015121,9.409603001,10.34816126,11.24274522,12.08733357,12.87899113\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.397493176,8.398274262,9.380097099,10.32772251,11.23077572,12.08299434,12.88134192\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,7.815425201,8.583042187,9.341846874,10.0884729,10.81884575,11.52881977,12.21467019\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.912293161,10.62607608,11.32598112,12.00660315,12.66348963,13.29329834,13.89376974\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.46869321,10.16989056,10.86757396,11.55359331,12.22134756,12.86578376,13.48329233\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.585680683,10.27294717,10.95674246,11.62976709,12.28585449,12.92012519,13.5289852\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,9.938043659,10.65285212,11.35221326,12.03146795,12.68668155,13.31483858,13.91386442\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,11.09026616,11.84168114,12.5772314,13.29074383,13.97661019,14.63050098,15.24954669\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.92090771,11.69570603,12.45072134,13.18050993,13.8800616,14.54553077,15.17443638\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.72792432,11.50441873,12.26061393,12.99118237,13.6912076,14.35691913,14.98589538\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.96748145,11.71972655,12.45579701,13.16963044,13.85569592,14.50971576,15.12885376\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.72987455,11.51861396,12.2809638,13.01343822,13.71283276,14.37672528,15.00364354\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,11.72548366,12.41292406,13.08474617,13.73571062,14.36152791,14.95901327,15.52607387\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.70323398,11.50634701,12.28088348,13.02348473,13.73110424,14.40150564,15.03341875\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,11.71432987,12.40135411,13.07312033,13.72414038,14.3499719,14.94734455,15.51412644\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.70340867,11.50648164,12.28098189,13.0235849,13.73126499,14.40179495,15.03390497\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,11.81906271,12.50388442,13.17376763,13.82315919,14.44756802,15.0436869,15.60935567\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,10.52874238,11.31383725,12.07279992,12.80215648,13.49870297,14.16000902,14.78458828\n\"linker n1ccc(cc1)C1C(c2ccncc2)C(C1c1ccncc1)c1ccncc1, n1ccc(cc1)C=Cc1ccncc1, nodes [Zn], topology pcu\",,,11.75841517,12.4403522,13.10760062,13.75469619,14.377192,14.9717905,15.5363163\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,20.79215664,21.22842506,21.57281658,21.84890295,22.07330641,22.25797034,22.41162803\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,20.88753186,21.305628,21.63559168,21.90007102,22.11502055,22.29189574,22.43906902\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,20.85994232,21.27828442,21.60836481,21.87288584,22.08783386,22.26468325,22.41181768\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,20.79293075,21.2291262,21.57345901,21.84949765,22.0738619,22.25849332,22.41212379\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,20.88660282,21.30476629,21.63478282,21.89930433,22.114288,22.2911912,22.43838771\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,20.8593028,21.27758024,21.60761107,21.87209337,22.08701059,22.26383511,22.41094918\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,3.386270197,4.0761134,4.782748556,5.489036596,6.182009737,6.852637564,7.495242203\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,3.384158966,4.073822549,4.780388609,5.486685037,6.179719052,6.850443369,7.493169795\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,3.381083635,4.070608675,4.777098277,5.483365685,6.176404738,6.847156419,7.489922494\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,3.386145406,4.075983956,4.782614182,5.488897459,6.18186624,6.852490204,7.495091484\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,3.384282453,4.073948185,4.78051346,5.486806897,6.179836363,6.850555097,7.493275301\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,3.381019519,4.070534257,4.777015537,5.483276425,6.176310324,6.847057646,7.48981955\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.295576247,8.160791354,9.006580944,9.829236848,10.6251399,11.3909825,12.1240327\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.802381753,8.603700629,9.39456313,10.17050972,10.92671561,11.65867964,12.36264538\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,9.316688661,10.13470549,10.91942817,11.66860822,12.38088494,13.05560769,13.69272263\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,6.714137756,7.519464152,8.318138574,9.104439531,9.873428608,10.62079408,11.34289613\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.289805234,8.154862077,9.000430383,9.822844558,10.61849923,11.38408818,12.11687688\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.783540631,8.583075117,9.3726926,10.14782405,10.90354071,11.63525364,12.33913687\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,9.282974021,10.0991338,10.88283288,11.63160159,12.34389561,13.01892264,13.6565244\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,6.706574433,7.511212568,8.309307271,9.095163221,9.863829943,10.61096993,11.33291604\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.282548116,8.145451107,8.989131906,9.809934032,10.60425807,11.36879391,12.10079288\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.782624173,8.5813655,9.37031452,10.14489931,10.9001862,11.63157978,12.33524602\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,9.277293247,10.09310906,10.87657494,11.62521915,12.33748862,13.01257943,13.65032057\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,6.698599699,7.50353943,8.301507812,9.086987938,9.855162448,10.6017893,11.32326583\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.295216434,8.160450333,9.006255937,9.828925361,10.6248397,11.39069163,12.12374945\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.801161394,8.602476347,9.393334205,10.16927604,10.92547746,11.65743753,12.36139994\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,9.315561307,10.13357835,10.91830164,11.66748277,12.37976099,13.05448556,13.69160253\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,6.71317222,7.518495102,8.317165994,9.103463464,9.872449155,10.61981138,11.34191036\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.289539167,8.154591972,9.000157891,9.822570626,10.61822444,11.3838129,12.11660139\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.783175029,8.582709581,9.3723262,10.14745631,10.90317151,11.63488307,12.33876512\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,9.282881153,10.09903998,10.88273926,11.63150884,12.34380409,13.01883247,13.65643557\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,6.706079012,7.51071932,8.308815112,9.094671291,9.863337614,10.61047678,11.33242183\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.281427382,8.144325535,8.988001587,9.808799068,10.60311858,11.36765006,12.09964486\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,7.781587123,8.580318627,9.369258848,10.14383578,10.89911568,11.63050306,12.3341638\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,9.277491563,10.09331261,10.87678253,11.62542989,12.33770183,13.01279452,13.65053708\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,6.697217852,7.502162277,8.300136286,9.085622555,9.853803356,10.60043636,11.32191868\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,17.46002,17.86794329,18.19132329,18.45445552,18.67465809,18.86441587,19.03275753\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,12.57748631,12.67934604,12.76258111,12.8343026,12.89978443,12.96291137,13.02645981\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,17.89725986,18.31176632,18.64039063,18.90774724,19.13138811,19.32397135,19.49465539\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,19.63392458,19.76480948,19.8704194,19.95973357,20.03928432,20.11382863,20.18676262\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,17.93748375,18.34488062,18.66785505,18.93066819,19.15061416,19.3401609,19.50832493\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,19.62457636,19.75692894,19.86368522,19.95391768,20.03422204,20.10939891,20.18287469\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,17.44701436,17.85512342,18.17865276,18.44190625,18.66220827,18.85204843,19.02045892\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,12.67975087,12.78169139,12.86498834,12.93675831,13.00227886,13.06543724,13.1290116\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,17.89627401,18.31086035,18.6395476,18.90695447,19.13063601,19.32325248,19.49396396\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,19.63467798,19.76545726,19.87098475,19.96023334,20.03973104,20.11423175,20.18712942\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,17.93701093,18.34433319,18.66724703,18.93001048,19.14991522,19.33942736,19.50756204\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,19.62517728,19.75747327,19.86418463,19.95438086,20.03465553,20.1098077,20.1832627\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.66931474,14.72378011,15.65036067,16.46597681,17.18567339,17.82248118,18.38755916\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.31537298,15.1601081,15.91663804,16.5962943,17.20857324,17.76147888,18.2618172\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.92324911,15.68687086,16.37237399,16.98981809,17.54772392,18.05326042,18.51247051\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.54647131,14.60956234,15.54440439,16.36771301,17.09445038,17.73763557,18.30845453\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.11400209,14.97898121,15.75297705,16.44781173,17.07335338,17.63789861,18.14849032\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.94772385,15.70457617,16.38428353,16.99681775,17.55058097,18.0526209,18.50887003\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.73583636,14.78059064,15.69900856,16.507743,17.22160088,17.85341634,18.41419113\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.83305823,14.72206508,15.51835051,16.23357897,16.87762542,17.4588813,17.9845265\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.94276371,15.70099428,16.3814506,16.99441591,17.54846743,18.0507482,18.50723998\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.66569866,14.72050942,15.64739707,16.46328402,17.18321851,17.8202351,18.38549644\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.31472031,15.15945043,15.91597434,16.5956242,17.20789671,17.76079607,18.26112836\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.92226673,15.68586853,16.37135481,16.98878444,17.54667771,18.0522032,18.5114036\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.5474658,14.61036333,15.54504569,16.36822222,17.09484983,17.73794325,18.308685\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.11343878,14.97842943,15.75244004,16.44729057,17.07284802,17.63740832,18.14801408\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.94644631,15.70330082,16.38301061,16.99554723,17.54931271,18.05135475,18.50760583\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.73453603,14.77925922,15.69764843,16.50635696,17.22019174,17.85198676,18.41274348\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,13.8329314,14.72192551,15.51820061,16.23342067,16.87746018,17.45871028,17.98435056\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Co], topology kgd,\",,,14.93881956,15.69707985,16.37755686,16.99053671,17.54459849,18.04688648,18.50338326\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,22.87193845,22.99134702,23.08392332,23.15708956,23.21588427,23.26382033,23.30340467\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,22.8719229,22.99133399,23.08391225,23.15708004,23.21587601,23.26381309,23.30339828\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,22.7587883,22.89502716,23.00109698,23.08521243,23.15299179,23.20837696,23.25419629\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,22.75230163,22.88956066,22.99643171,23.08118671,23.14948409,23.20529439,23.25146673\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,22.75877593,22.89501678,23.00108814,23.08520481,23.15298516,23.20837114,23.25419115\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,22.75230654,22.88956483,22.99643529,23.0811898,23.14948679,23.20529677,23.25146883\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.40979046,4.074691488,4.761911228,5.453923134,6.136982795,6.801200625,7.44010571\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495769351,4.142722687,4.810584088,5.483243162,6.148032015,6.795750955,7.420285591\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.496694974,4.141908891,4.808221954,5.479608174,6.143394717,6.79033882,7.414273261\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.409717691,4.074616124,4.761833822,5.45384442,6.136903539,6.801121541,7.440027416\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495808592,4.142763253,4.810625336,5.483284515,6.148072979,6.795791127,7.420324649\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.496728604,4.141942934,4.808256018,5.479641946,6.143427947,6.790371311,7.414304858\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.405436527,4.070782694,4.758503171,5.451022937,6.134566591,6.799227139,7.4385258\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495399146,4.14262361,4.810756997,5.483668286,6.148676608,6.796575502,7.421248245\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.494290483,4.139744805,4.806320631,5.47797252,6.14201371,6.789192329,7.413335883\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.40546708,4.070820029,4.75854636,5.451070885,6.134618192,6.799281359,7.438581728\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495378401,4.14260076,4.810732367,5.483642224,6.148649479,6.796547671,7.421220061\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.494195384,4.139653003,4.806232453,5.477888134,6.141933188,6.78911568,7.413263072\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.409772542,4.074676339,4.76189861,5.453912775,6.136974414,6.801193947,7.44010048\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495768995,4.142720033,4.810580141,5.48323869,6.148027581,6.795746974,7.420282374\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.496758046,4.141973934,4.808288215,5.479674913,6.14346127,6.790404628,7.414337879\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.409767786,4.074671943,4.761894691,5.453909415,6.136971649,6.80119177,7.440098854\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495818282,4.142773015,4.810635199,5.483294475,6.148082974,6.795801036,7.420334303\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.496790105,4.142007208,4.808321622,5.479707707,6.143492949,6.790434852,7.41436642\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.405474802,4.070827814,4.75855393,5.451078116,6.134625034,6.799287802,7.438587775\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495398191,4.142619188,4.810749596,5.483658404,6.148664696,6.796561935,7.421233305\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.494242732,4.13969839,4.806276106,5.477930218,6.141973795,6.789154843,7.413300781\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.40545446,4.070803999,4.758527579,5.451049988,6.13459575,6.799257868,7.438557603\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.495365242,4.142587527,4.810719312,5.483629559,6.148637395,6.796536355,7.421209703\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.494240987,4.139695817,4.806272379,5.477925206,6.141967521,6.789147442,7.413292459\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.074908274,8.854684089,9.625182841,10.38238887,11.1218064,11.83908179,12.5304476\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.530324689,10.32775987,11.09827402,11.83821407,12.54488043,13.21650485,13.85217262\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.970841701,8.764064823,9.54782011,10.31772489,11.06894552,11.79690528,12.49773437\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.586569265,8.425831253,9.257865518,10.07474453,10.86959294,11.63681971,12.3722076\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01982294,10.78711034,11.52344129,12.2278146,12.8994216,13.53769766,14.14240034\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.922049517,10.68155996,11.41530731,12.12078175,12.79586747,13.43900683,14.04926125\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.27522029,8.081093546,8.877054596,9.657912326,10.41920992,11.1570853,11.8683125\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.328080227,8.120097882,8.905692382,9.678717884,10.43404258,11.16733184,11.87502428\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.074969769,8.854751271,9.625251692,10.38245685,11.12187197,11.83914409,12.53050619\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.530168898,10.32761816,11.09814086,11.83808592,12.5447552,13.2163814,13.85205047\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.97081988,8.764030951,9.547774503,10.31766837,11.06887928,11.79683072,12.49765296\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.58670993,8.425967849,9.25799974,10.07487669,10.86972277,11.63694674,12.37233136\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01993954,10.78722177,11.52354534,12.22790999,12.89950784,13.53777482,14.14246884\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.921985408,10.68150835,11.41526514,12.12074669,12.79583779,13.43898127,14.04923888\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.275081846,8.080942209,8.876895808,9.657749113,10.41904413,11.15691824,11.86814519\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.328454226,8.120414611,8.905963045,9.678950838,10.43424431,11.16750753,11.87517812\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.08031532,8.860066121,9.630593582,10.38785204,11.12732201,11.84463411,12.53601217\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.523348781,10.32108714,11.09196195,11.83228965,12.5393497,13.21136001,13.84739729\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.962831496,8.756651141,9.540917619,10.31127555,11.06290661,11.79124283,12.49241961\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.572105925,8.412165536,9.245017233,10.06269013,10.85828802,11.62621206,12.36224423\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01905028,10.78633645,11.52266431,12.22703621,12.89864468,13.53692532,14.1416355\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.918207722,10.67775782,11.41160138,12.11721259,12.79246146,13.4357788,14.04621724\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.280724248,8.085399412,8.880434782,9.660550427,10.42123905,11.15860842,11.86941308\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.344765575,8.131679898,8.913711467,9.684280664,10.43793946,11.17012222,11.87709948\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.080191998,8.859962974,9.630509827,10.3877863,11.12727256,11.84459907,12.53598963\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.523356194,10.32110227,11.09198565,11.8323219,12.5393899,13.21140728,13.84745057\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.962850738,8.756675661,9.540947784,10.31131118,11.06294722,11.79128772,12.49246803\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.572043456,8.412111854,9.244969714,10.06264724,10.85824884,11.62617598,12.36221083\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01895926,10.78625189,11.52258856,12.22697034,12.89858891,13.5368793,14.14159854\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.918089213,10.67765903,11.41151976,12.11714586,12.79240755,13.4357359,14.04618373\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.280944743,8.085606217,8.880628581,9.66073237,10.42141036,11.15877025,11.86956639\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.344650897,8.131571833,8.913613081,9.684193234,10.43786315,11.17005652,11.87704356\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.075003501,8.854775639,9.625271043,10.38247388,11.12188829,11.83916057,12.53052328\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.530284611,10.32772839,11.09824949,11.83819515,12.54486604,13.21649412,13.85216483\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.970838464,8.764065064,9.547823995,10.31773235,11.06895632,11.79691906,12.49775071\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.586555098,8.425820531,9.257857182,10.07473795,10.86958772,11.63681558,12.37220437\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01988743,10.78716712,11.52349182,12.22785997,12.89946265,13.53773506,14.14243462\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.922098047,10.68159912,11.41533918,12.12080786,12.79588898,13.43902463,14.04927604\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.275282718,8.081146949,8.877099252,9.657948942,10.41923938,11.15710853,11.86833039\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.328064923,8.120096247,8.905700772,9.678733635,10.43406372,11.16735688,11.87505209\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.074938651,8.854721871,9.625224108,10.382431,11.12184768,11.83912114,12.53048438\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.530213611,10.32765353,11.09816811,11.83810608,12.54476919,13.21639006,13.85205455\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.970832717,8.764039404,9.54777877,10.31766877,11.0688762,11.79682459,12.49764424\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.586724798,8.425981573,9.258013386,10.07489076,10.86973745,11.63696203,12.37234716\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01991919,10.78720599,11.52353333,12.22790117,12.89950174,13.53777101,14.14246695\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.92195527,10.68147961,11.41523773,12.12072054,12.79581284,13.43895744,14.0492161\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.275035144,8.080903178,8.876863156,9.657721525,10.41902045,11.1568975,11.86812665\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.328492859,8.120438132,8.905974915,9.678953676,10.43424014,11.16749794,11.87516437\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.080268469,8.860025538,9.630559208,10.38782357,11.12729899,11.84461597,12.53599832\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.523290936,10.32103638,11.09191742,11.83225059,12.53931545,13.21132997,13.84737092\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.962834287,8.756653055,9.540918153,10.31127446,11.06290385,11.79123846,12.49241378\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.572083563,8.412144686,9.244997554,10.06267146,10.85827028,11.62619521,12.36222824\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01903726,10.78631928,11.52264474,12.22701546,12.89862357,13.5369044,14.14161509\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.918187704,10.67774164,11.4115882,12.11720176,12.79245244,13.4357712,14.04621073\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.280737138,8.08540851,8.880440882,9.660554316,10.42124141,11.15860982,11.86941393\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.34470074,8.131622939,8.913661846,9.684237768,10.43790263,11.17009078,11.87707279\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,8.080249092,8.860014635,9.630556554,10.38782855,11.12731075,11.84463358,12.53602083\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.523401835,10.32114123,11.09201863,11.83234953,12.5394128,13.21142601,13.84746568\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.96286706,8.756691645,9.540963719,10.31132724,11.06296346,11.79130416,12.49248462\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.572049975,8.41211493,9.244969422,10.06264374,10.85824239,11.62616691,12.36219951\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,10.01899525,10.78628687,11.52262163,12.22700099,12.89861689,13.53690457,14.14162117\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.918112848,10.67767751,11.41153413,12.11715694,12.79241597,13.43574216,14.04618821\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.280937569,8.08560294,8.880628917,9.660735878,10.42141655,11.15877862,11.86957648\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.344665161,8.131582202,8.913620372,9.6841982,10.43786643,11.17005862,11.87704487\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.25597358,8.148935531,9.019947534,9.861529059,10.66910582,11.44000413,12.17283061\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.259417792,8.152831755,9.024311454,9.866346158,10.67433864,11.44560021,12.17872952\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.256002466,8.148955235,9.019956379,9.861525691,10.66908941,11.43997443,12.17278789\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.259412522,8.15282265,9.024297098,9.866325373,10.67431062,11.44556456,12.17868624\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.27585984,16.03698124,16.71679165,17.32704355,17.87724975,18.37512075,18.82696875\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.40494738,16.1812454,16.8633835,17.4687967,18.01041595,18.49799682,18.93905898\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.16664365,16.85057853,17.4569325,17.99976325,18.48923439,18.93290449,19.33658097\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.57053933,16.29853815,16.94197308,17.5162159,18.03271103,18.50009484,18.92500959\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.28755597,16.04733068,16.72599503,17.33526692,17.88463103,18.38177496,18.83299215\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.39846357,16.17546887,16.85821673,17.46415517,18.00622788,18.49420177,18.93560612\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.1774095,16.85991364,17.46508489,18.00693013,18.49557372,18.93854377,19.34162397\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.56652255,16.29498809,16.93882914,17.51342386,18.03022356,18.49787117,18.92301478\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.17436154,15.94577477,16.63490941,17.25346119,17.81098597,18.31528185,18.77276298\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.64139824,16.38942534,17.04762591,17.63272377,18.15702695,18.62977061,19.05804849\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.65455943,17.2776347,17.83377798,18.33477444,18.78904817,19.20282682,19.58089533\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.63780157,16.35135868,16.98440427,17.55101083,18.06177316,18.52476461,18.94624863\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.16546525,15.93789169,16.62789571,17.24719502,17.8053644,18.31021803,18.76818359\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.64847484,16.39570513,17.05322379,17.63773729,18.16153796,18.63384753,19.06174854\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.64719059,17.27125271,17.82821678,18.32989972,18.78475099,19.19901842,19.57750296\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.64710684,16.35958828,16.99170936,17.55752082,18.06759786,18.52999691,18.95096706\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.27349491,16.0348711,16.7149025,17.32534604,17.87571868,18.37373461,18.82570922\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.40670819,16.18281941,16.86479515,17.4700676,18.01156472,18.49903931,18.94000859\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.16380237,16.84811059,17.45477096,17.99785543,18.48753862,18.93138754,19.33521614\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.57109285,16.299037,16.94242376,17.51662454,18.03308304,18.50043486,18.92532159\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.2897945,16.04932091,16.72777078,17.33685722,17.88606069,18.38306508,18.83416066\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.39667404,16.17387258,16.85678732,17.46286975,18.00506699,18.49314897,18.93464759\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.18025264,16.86238146,17.46724443,18.0088342,18.49726412,18.94005391,19.34298077\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.56611626,16.29462081,16.93849703,17.51312296,18.02995016,18.49762195,18.92278685\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.1732642,15.94479725,16.63403569,17.25267736,17.81028009,18.31464372,18.77218395\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.64211399,16.39006542,17.04820101,17.63324306,18.15749811,18.63020006,19.05844156\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.65365889,17.27685816,17.8331041,18.33418618,18.78853182,19.20237123,19.58049138\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.63812027,16.3516388,16.98465093,17.55122845,18.06196554,18.52493506,18.94640002\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.16662026,15.93892013,16.62881381,17.24801714,17.80610301,18.31088391,18.76878598\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.64769801,16.39501711,17.05261219,17.6371914,18.16104866,18.63340711,19.06135052\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.64789484,17.2718656,17.82875362,18.33037284,18.78517035,19.19939213,19.57783766\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.64665347,16.35919188,16.99136109,17.55721352,18.06732563,18.52975484,18.95075103\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.34237013,16.99516607,17.56051619,18.05685207,18.49812625,18.89477753,19.25457866\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.29564861,16.95561115,17.52671568,18.02773734,18.47287367,18.87274143,19.23524514\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.34254686,16.99531491,17.56063962,18.05695217,18.49820494,18.89483668,19.25462016\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,16.29564489,16.95560457,17.52670507,18.02772187,18.47285285,18.87271512,19.23521346\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,17.16874869,17.36777243,17.52284322,17.64589192,17.74509721,17.82620422,17.89333765\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,18.32795082,18.51796197,18.66679188,18.78538619,18.88132647,18.95998367,19.02524069\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.254945123,3.89915224,4.566239019,5.240275599,5.908506739,6.561551902,7.193101762\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.072306096,3.726494967,4.401065695,5.080427972,5.752328334,6.407832752,7.040953492\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,2.852721108,3.505943109,4.188231587,4.880644331,5.568356642,6.240599701,6.89015411\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.452930934,4.041522103,4.648926871,5.264686517,5.879395322,6.485400474,7.077013217\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.043634208,3.554221251,4.095833497,4.659636413,5.236465331,5.817984757,6.397280988\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,2.937890443,3.379134495,3.858537087,4.368521921,4.900015161,5.44398804,5.992400047\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.791589144,4.34956376,4.927934897,5.517415777,6.109226541,6.695983774,7.272035398\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.445890003,4.040319766,4.649605179,5.264780483,5.877526863,6.480912454,7.069686198\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,2.504171632,2.981559669,3.498591842,4.047323692,4.618875591,5.204702663,5.797302367\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,2.466371555,3.022731313,3.624374465,4.255326583,4.901331982,5.550821488,6.195063113\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.215920581,3.886751188,4.573017837,5.259721997,5.935258516,6.591294944,7.222362026\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,2.99877816,3.649067312,4.32453065,5.007730115,5.684980934,6.346298095,6.984954093\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.702916008,4.241775595,4.808886795,5.392628098,5.982054076,6.567952799,7.143228687\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.455725372,3.98090914,4.535291124,5.108291143,5.689603035,6.270280002,6.843211518\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.363621203,3.810389638,4.295281854,4.809476986,5.342987394,5.886219664,6.430870412\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,4.143528709,4.680781994,5.239558926,5.810439769,6.384318825,6.953429555,7.511766216\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,3.62241026,4.214914778,4.820034749,5.429652176,6.035998468,6.632493143,7.214107464\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,2.595235024,3.05705407,3.556420365,4.086475275,4.638952213,5.205593308,5.778998755\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,7.221062562,8.026568413,8.813318761,9.579733122,10.32385021,11.04343878,11.73629988\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,9.080207137,9.853658259,10.59828959,11.31336874,11.99774262,12.65038187,13.27063152\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,7.748441174,8.516278777,9.263901686,9.991394615,10.69792858,11.38202892,12.04196661\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,9.028851568,9.834539417,10.61002496,11.35350091,12.06317917,12.73773495,13.37646608\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,7.386107823,8.164198742,8.926676865,9.672449709,10.3994311,11.10499648,11.78647362\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,9.101834575,9.904024269,10.67863726,11.42239426,12.13257067,12.80728904,13.44555851\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,8.858381972,9.740502594,10.59149876,11.40375837,12.17254075,12.89544926,13.5718859\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,6.591114594,7.315315677,8.042514197,8.768848301,9.489254626,10.1982843,10.89076915\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,8.980455393,9.827270184,10.65201194,11.44559964,12.20168552,12.91641588,13.58798604\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,6.828001518,7.557225543,8.285423007,9.009719147,9.726025159,10.42977567,11.11653771\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,8.246553072,9.140569247,10.00700691,10.83806605,11.62844349,12.37505496,13.07662411\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,6.610279346,7.343675548,8.076970574,8.806046213,9.526497855,10.23385632,10.92390998\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,7.459979852,8.282513249,9.083574238,9.861882783,10.6155515,11.34239475,12.04030811\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,9.082632675,9.872940763,10.63381832,11.36437188,12.06322095,12.72913938,13.36134973\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,7.705879206,8.494568358,9.264318257,10.01411971,10.74215728,11.44618729,12.12396256\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,8.893134965,9.704997869,10.48663808,11.23633375,11.95229254,12.63312186,13.27802319\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,7.435058568,8.217231739,8.981957338,9.728817544,10.45621376,11.16185058,11.84326376\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,9.104247613,9.89817605,10.6647452,11.40163794,12.10658323,12.77782877,13.41431167\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,9.06815883,9.969391206,10.84246302,11.67669396,12.46532512,13.20481739,13.89407795\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,7.005878279,7.73134623,8.456274527,9.17667287,9.888072258,10.58592822,11.26600824\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,8.826178855,9.683022763,10.51989845,11.32592202,12.09368547,12.81876634,13.4991073\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,6.953267147,7.664466658,8.376287514,9.086056359,9.789702663,10.48256788,11.16006592\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,8.333335983,9.24104396,10.11845281,10.95784531,11.75416814,12.5046569,13.2083679\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,6.732877908,7.465774338,8.20468548,8.943643584,9.676468108,10.39719982,11.10049773\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,13.61049088,14.29564889,14.91121212,15.46782699,15.97348471,16.43437366,16.85544979\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,13.83397395,14.55766435,15.2076058,15.79459609,16.32691997,16.81113667,17.25259604\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.10427575,15.01856313,15.83051691,16.5540214,17.20057438,17.77980374,18.29987148\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.56970295,15.35844914,16.05562741,16.67686581,17.23420586,17.73703861,18.19279019\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.67058538,15.46716109,16.17244174,16.80141429,17.36568799,17.8743711,18.33473092\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.72028186,15.48767117,16.17130216,16.78406585,17.33618418,17.83580369,18.28949439\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,15.27703595,16.03616548,16.7139948,17.32249874,17.87076831,18.36604881,18.81434164\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.90818352,15.61297843,16.24537842,16.81611962,17.33375282,17.80514824,18.23588021\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.78567366,15.62639377,16.37372858,17.04078964,17.63815088,18.17451604,18.65719071\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.76951625,15.51907757,16.18422687,16.77912758,17.31468482,17.79940244,18.2400092\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.86141213,15.66342888,16.37428031,17.00841564,17.57707624,18.08915787,18.5518421\n\"linker [O-]C(=O)Cc1cc(CC(=O)[O-])cc(c1)CC(=O)[O-], nodes [Gd], topology \",,,14.46865864,15.29382925,16.0275292,16.68301231,17.27114721,17.80083346,18.27940645\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,20.30786899,20.70418051,21.01795586,21.27016577,21.47564507,21.64508806,21.78633979\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,20.30386218,20.70080284,21.01507108,21.2676744,21.47347268,21.64317783,21.78464754\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,20.30382464,20.70077196,21.01504526,21.26765249,21.47345387,21.64316151,21.78463325\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.45834499,8.045806326,8.597309632,9.117833864,9.609536715,10.0732362,10.50930003\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,3.688517253,4.39732356,5.115415861,5.826601079,6.519125775,7.18517806,7.820171425\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.466466106,8.053364211,8.60432192,9.124332997,9.615560065,10.0788215,10.51448339\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,3.690415014,4.399343237,5.117478499,5.828648293,6.521117474,7.187088752,7.821986516\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.451247609,8.039602853,8.591866985,9.113035832,9.605284936,10.06944861,10.50590857\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,3.688887045,4.397668575,5.115709499,5.826828403,6.51928091,7.185261458,7.820187544\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.46704746,8.053634088,8.604379569,9.124248916,9.615384053,10.07858857,10.51421802\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,3.688462668,4.397250634,5.115326205,5.826497027,6.519009985,7.185053209,7.82004002\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.465832879,8.052805584,8.603831631,9.123903646,9.615184155,10.07849198,10.51419389\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,3.690542963,4.399490951,5.117643462,5.828827335,6.521307223,7.187285963,7.822188256\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.455273024,8.043231915,8.595153552,9.116026792,9.608019588,10.07195948,10.50822256\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,3.689161942,4.397965447,5.11602005,5.827145622,6.519599208,7.18557658,7.820496377\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.688433543,8.47468028,9.240015424,9.984287987,10.70643102,11.40475481,12.07737182\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,9.338680511,10.13519466,10.90300266,11.63842954,12.33908575,13.00364408,13.63163482\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.686555335,8.473006215,9.23853155,9.982974255,10.70526583,11.40371747,12.07644374\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,9.336287682,10.13304788,10.90106545,11.63667006,12.33747723,13.00216454,13.63026644\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.687348203,8.473707221,9.239148214,9.983517315,10.70574642,11.40414582,12.07682866\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,9.337509678,10.13417468,10.90210103,11.63762307,12.33835749,13.00298137,13.63102795\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.688419455,8.474659568,9.239990797,9.984261617,10.70640457,11.40472946,12.07734839\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,9.338669011,10.13518006,10.9029859,11.63841139,12.33906682,13.00362483,13.63161558\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.686599896,8.473069526,9.238610697,9.983066472,10.70536854,11.40382832,12.07656065\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,9.336350904,10.13311324,10.90113271,11.63673882,12.33754701,13.00223484,13.63033675\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.687343318,8.473717069,9.239172944,9.983556416,10.70579887,11.40421026,12.07690355\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,9.33754896,10.1342269,10.90216596,11.63769974,12.33844449,13.00307708,13.63113072\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,6.347057428,7.129625758,7.915823564,8.697178432,9.466607108,10.21815882,10.94696205\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.22101814,7.977037951,8.729205267,9.473641638,10.2056682,10.92051816,11.6138678\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.655067288,8.44388568,9.222241671,9.985513247,10.72928655,11.44955637,12.1429539\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,6.34702806,7.129600163,7.915800332,8.697156562,9.466585937,10.21813794,10.94694123\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.221064923,7.977059922,8.729204869,9.473621712,10.2056317,10.92046797,11.61380658\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.655088273,8.443897087,9.222244282,9.985508087,10.72927474,11.44953904,12.14293211\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,6.34967277,7.132200901,7.918288527,8.699485881,9.468730057,10.22008617,10.94869401\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.221953313,7.977857814,8.729935195,9.4743053,10.20628502,10.92110274,11.61443038\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,7.655868034,8.444974711,9.223509158,9.986882253,10.73070391,11.45098576,12.14437075\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.2118773,15.93598287,16.58744303,17.1753207,17.7072402,18.18963575,18.62798038\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.93400272,16.66193782,17.30127095,17.86626649,18.36802631,18.81538498,19.21553576\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.18222547,15.9097619,16.56416441,17.15456735,17.68865909,18.17292918,18.61289758\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.94394814,16.67054154,17.30877102,17.87285074,18.37384438,18.82055723,19.22015981\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.18716618,15.91448172,16.56865424,17.15881352,17.69265272,18.17666847,18.61638712\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.93811079,16.66583549,17.30492797,17.86967326,18.37118584,18.8183077,19.21823603\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.21219283,15.93625371,16.58767746,17.17552521,17.70741995,18.18979482,18.62812206\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.93438768,16.66226445,17.30155309,17.86651433,18.36824722,18.81558434,19.21571749\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.18292733,15.91038562,16.56472223,17.15506911,17.68911277,18.17334132,18.61327357\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.94470179,16.67121131,17.30936778,17.87338445,18.37432372,18.82098957,19.22055137\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.18805105,15.91527981,16.56937861,17.15947495,17.69325999,18.1772287,18.61690608\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,15.9384683,16.66615343,17.30521336,17.86993172,18.37142175,18.81852443,19.21843622\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,13.50880438,14.49294023,15.37082628,16.15295568,16.84990252,17.47160703,18.02707811\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,13.50869006,14.49282496,15.37071208,16.1528439,16.84979401,17.47150233,18.02697753\n\"linker [O-]C(=O)c1cc(O)c(c(c1)O)[O], nodes [Mn], topology sod\",,,13.51743997,14.50142783,15.37909751,16.16096181,16.85761112,17.47899867,18.0341434\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,20.37163441,20.74081363,21.03482207,21.2722743,21.46649777,21.62719403,21.7615366\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,20.37094663,20.74024306,21.03434086,21.27186283,21.46614178,21.62688293,21.76126236\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,19.75297288,20.20988767,20.57518225,20.87108695,21.11368905,21.31479114,21.48317209\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,19.75297693,20.20989117,20.57518527,20.87108959,21.11369135,21.31479317,21.48317389\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,3.373456971,4.04534019,4.741101303,5.44205275,6.133649319,6.805525261,7.450980952\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,3.415829209,4.072366959,4.752180466,5.437734323,6.115265713,6.774842675,7.409929044\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,3.434446031,4.09528461,4.778579059,5.466819532,6.14632801,6.807288691,7.443291341\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,1.484413534,1.914515142,2.423087756,2.998501283,3.626676568,4.293303898,4.985152601\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,3.373452936,4.045346654,4.741113439,5.442067346,6.133664345,6.805539508,7.450993757\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,3.415778059,4.07232259,4.752139857,5.437695439,6.115227263,6.774803901,7.40988955\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,3.434565359,4.095371567,4.778640085,5.466859895,6.146352001,6.807299787,7.443292344\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,1.484254321,1.914530037,2.423260087,2.998812174,3.627106316,4.293833145,4.98576317\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,6.719585561,7.473813575,8.227477016,8.97509156,9.711552757,10.4321306,11.1326257\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,7.776645012,8.548350397,9.307552693,10.05167236,10.77747692,11.48158309,12.16088724\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.236520439,10.0192851,10.78015009,11.51436681,12.21814423,12.88882165,13.52482209\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,7.799229988,8.575363739,9.338808503,10.08692658,10.81638375,11.52370345,12.20572047\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.347660534,10.1131028,10.85875471,11.57984866,12.2724479,12.93368553,13.56175977\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,7.297462729,8.128791381,8.942814174,9.735298429,10.50273698,11.24217823,11.95125066\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.325841289,10.09417875,10.84136712,11.56314797,12.25593913,12.91711169,13.54501788\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,6.672880109,7.445027035,8.214735617,8.975491536,9.721872329,10.44926842,11.15384077\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,6.835369607,7.594279146,8.357095965,9.117642839,9.869292766,10.6057456,11.3215291\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,6.720237737,7.474213424,8.227689459,8.975165997,9.711526891,10.43203315,11.13247842\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,7.775959533,8.54775637,9.307035174,10.05121962,10.77707949,11.48123316,12.16057825\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.23563471,10.01854474,10.77952784,11.51384139,12.21769878,12.88844265,13.52449857\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,7.798346174,8.574549321,9.338051023,10.0862167,10.81571471,11.52307041,12.20511989\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.348352583,10.11381254,10.85946542,11.58054862,12.27312922,12.93434315,13.56239073\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,7.298233357,8.129442066,8.943368005,9.73577342,10.50314729,11.24253507,11.95156299\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.32727776,10.09543001,10.84246574,11.5641197,12.25680443,12.91788698,13.54571644\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,6.671754806,7.444194487,8.214118939,8.97503327,9.721529661,10.44900961,11.15364242\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,6.835203831,7.594118045,8.356941958,9.117497047,9.869155562,10.60561692,11.32140864\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,10.03643257,10.83328875,11.61121213,12.36562891,13.09154154,13.78468043,14.44198474\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.481276461,10.24508746,11.00206232,11.74626282,12.47101035,13.17026937,13.83930327\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,10.03668588,10.83348735,11.61137359,12.36576455,13.09165875,13.78478408,14.44207809\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.482308835,10.24595446,11.00279761,11.74689196,12.47155303,13.17074098,13.83971594\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,10.03667705,10.83347493,11.61135817,12.36574674,13.09163914,13.78476319,14.44205636\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.4823478,10.24599226,11.00283391,11.74692657,12.47158587,13.17077204,13.83974525\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,10.03646628,10.83331615,11.6112342,12.36564655,13.09155554,13.78469146,14.44199337\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,9.481170819,10.24499636,11.00198432,11.74619639,12.470954,13.17022172,13.83926306\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,14.910634,15.67076115,16.34687276,16.95226089,17.49730516,17.99021213,18.43757219\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,14.17330169,15.03656757,15.8052423,16.49245164,17.10900161,17.66385293,18.16450982\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,15.15362954,15.85850347,16.49402896,17.06912334,17.59115364,18.0662487,18.49956242\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,13.73298068,14.59387793,15.37075748,16.07214502,16.70601609,17.27960894,17.79938913\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,15.32709486,16.40725439,17.30882375,18.06558605,18.70525898,19.25006956,19.71766683\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,14.90743839,15.66793278,16.34442359,16.95017085,17.49553989,17.98873264,18.43633989\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,14.19359056,15.05469802,15.82149455,16.50706992,17.12219635,17.67580444,18.17537233\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,15.14486632,15.85093706,16.48743365,17.06332591,17.58601924,18.06167095,18.49545637\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,13.7067324,14.5705525,15.34991084,16.05341553,16.68910736,17.2642763,17.78542909\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cu], [OH], topology \",,,15.30938719,16.39164808,17.29502983,18.0533461,18.69435016,19.24030299,19.70888365\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,22.32321006,22.51000543,22.65551311,22.77099113,22.8641291,22.94031601,23.00341514\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,22.331286,22.5180397,22.66351734,22.77897301,22.87209392,22.94826753,23.0113561\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,22.30159811,22.48606448,22.62978683,22.74386757,22.83589201,22.9111774,22.97353648\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,22.30087954,22.48532604,22.62903285,22.74310125,22.83511576,22.91039304,22.97274542\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.684240087,4.385980785,5.10593887,5.82456653,6.527544273,7.205226297,7.851788523\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.188528729,5.817601109,6.417206359,6.99007152,7.537661959,8.060510685,8.558650935\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.189715862,5.818811234,6.418450447,6.991355626,7.538988595,8.061879919,8.560061232\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.927223302,4.653273249,5.388317476,6.114375033,6.818785214,7.493410807,8.133693502\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.914168343,4.640366582,5.375525679,6.101673527,6.806155412,7.480838258,8.121166676\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.937280623,4.662060291,5.395829179,6.12069206,6.824036457,7.497745274,8.137261616\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.24102358,3.902529176,4.587606165,5.278788184,5.962303178,6.628155148,7.269715525\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.685237558,4.388109962,5.109034382,5.828424459,6.531950293,7.209974302,7.856691299\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.185536864,5.820512011,6.425644108,7.003493109,7.555443854,8.082007476,8.58323468\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.171469299,5.806575311,6.411839004,6.989811203,7.541872294,8.068531798,8.569840464\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.680819136,4.382522143,5.102450451,5.821058318,6.524026497,7.201708291,7.848278144\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.239900622,3.901395404,4.586462239,5.277634776,5.961140986,6.626984864,7.268537794\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.681455812,4.383211723,5.103191723,5.821843424,6.52484444,7.202547281,7.849127003\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.239593825,3.901683971,4.587156079,5.278571614,5.962188652,6.62803938,7.269519766\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.685836756,4.38774935,5.107843978,5.826569175,6.529605238,7.207308011,7.85385592\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.937545591,4.662436614,5.396272342,6.121165006,6.824508334,7.4981899,8.137656127\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.686924042,4.389713763,5.110560062,5.829880311,6.533346582,7.211321779,7.858000171\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.237297843,3.899368176,4.584827686,5.276237481,5.959854667,6.625710257,7.267199069\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.210391107,5.839405119,6.438936844,7.011722486,7.559232545,8.082002792,8.580067866\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.212055543,5.847184054,6.452425046,7.030350325,7.582352093,8.108946537,8.610188189\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.694795353,4.397405266,5.118098843,5.837290534,6.540649736,7.218536669,7.865142917\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.693017514,4.395706892,5.116471899,5.83572424,6.539132348,7.217056799,7.863690355\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.910191378,4.636368758,5.371513243,6.097652467,6.802131377,7.476816483,8.117151943\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.21446145,5.843501262,6.443048297,7.015841285,7.563353394,8.086122708,8.584185648\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.233867817,3.895939824,4.581398689,5.2728065,5.956421134,6.62227413,7.263760621\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.938605813,4.663548261,5.397434548,6.122371119,6.825748796,7.499454234,8.138934183\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.929159188,4.655158478,5.390166534,6.116201736,6.820602051,7.49522865,8.135521564\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.241442511,3.902951816,4.588037934,5.279232066,5.962760364,6.628625615,7.270198481\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.239546994,3.901067117,4.586150146,5.277332168,5.960843066,6.626688298,7.268240344\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,5.210438535,5.84543086,6.450543489,7.028352062,7.580250553,8.106755508,8.607920923\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.939043291,4.664051481,5.397979605,6.122940319,6.826329142,7.50003625,8.139510995\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,3.23396413,3.896112464,4.581633705,5.273089202,5.956737552,6.622611817,7.264108988\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.229542823,9.89010224,10.55500045,11.21682646,11.86860852,12.50435674,13.11930285\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.244440356,10.07389665,10.8683672,11.62580517,12.34505359,13.02564449,13.66768399\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.795910454,8.609462375,9.4117115,10.19780278,10.9628136,11.70230127,12.41263981\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.49183411,8.343054222,9.179544121,9.995626282,10.78639418,11.54779031,12.27669606\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.388059398,10.04911865,10.71616943,11.38067885,12.03489634,12.67234893,13.28801845\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.207344597,10.03674385,10.83116625,11.58856466,12.30778132,12.98834724,13.63036748\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.077126309,7.883030297,8.676906774,9.452673925,10.2059075,10.93335243,11.63264462\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.378282999,10.03846681,10.70498084,11.3691916,12.02327536,12.66070506,13.27642276\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,6.980476015,7.785553036,8.578398786,9.352862437,10.1045489,10.83026525,11.52771324\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,6.964847818,7.736250657,8.502715115,9.258915892,10.00019408,10.72243341,11.42209946\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.476343138,8.327641053,9.164207971,9.980362964,10.77119773,11.53265402,12.26161313\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.409710603,10.07086693,10.73800898,11.4026012,12.05689131,12.69440563,13.31012607\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.22423298,9.885210651,10.55049631,11.21267748,11.86477996,12.50081224,13.11600579\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.375564592,8.22699524,9.063950422,9.880564192,10.67184085,11.43368631,12.16297185\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.091398086,7.897338333,8.691232602,9.467004462,10.22023404,10.94766981,11.64695038\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.21077248,10.04032521,10.83487434,11.5923767,12.31167798,12.99231222,13.63438713\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,6.974239036,7.745730671,8.512275766,9.268551653,10.00989984,10.73220351,11.43192746\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.40931844,10.0704457,10.73753569,11.40206728,12.05629722,12.69375713,13.30943168\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.394063945,8.245720752,9.082849069,9.89959338,10.69096646,11.45288123,12.18221476\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,6.962594634,7.733992312,8.500469102,9.256691814,9.997996987,10.72026554,11.41996122\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.227111627,10.05647207,10.85086152,11.60823201,12.32742512,13.00797127,13.64997501\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.498494679,8.349711278,9.186198308,10.00227885,10.79304646,11.55444347,12.28335102\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.16603382,9.826189205,10.49071459,11.15220259,11.80369173,12.4391998,13.05396155\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.032737056,7.838134245,8.631225408,9.405875998,10.15770307,10.88352305,11.58104502\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.48233246,8.33354302,9.170043902,9.986148269,10.77694374,11.53836918,12.26730385\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.317930168,10.14600416,10.93966138,11.69671366,12.41588344,13.09660865,13.7389252\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,6.651160071,7.455739142,8.248262093,9.022509315,9.774045702,10.49965455,11.19702311\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.337069486,8.188222982,9.024987673,9.841467019,10.63264725,11.39442327,12.12365933\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.402275218,10.0623888,10.72884672,11.39301295,12.04706167,12.68446409,13.30016079\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,6.957228209,7.728508253,8.494886026,9.251022551,9.992251494,10.71445247,11.41408863\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.008819652,7.777979,8.542946946,9.298182761,10.03887103,10.76078311,11.4603043\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.050931037,9.711878059,10.37702722,11.03901603,11.69091355,12.32675892,12.94180222\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,6.714686081,7.519246634,8.311746901,9.085980846,9.837517892,10.56314125,11.26053603\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.331183315,10.1591631,10.95273912,11.70972078,12.42882892,13.10950029,13.75176989\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.799573091,8.613093532,9.415318729,10.2013923,10.96639067,11.70587037,12.41620473\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.665771825,8.479591514,9.281946241,10.06804233,10.83300704,11.57243173,12.2827111\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.342013501,8.193231665,9.030062254,9.846599553,10.63782666,11.39963843,12.12890043\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.215631008,9.87639906,10.54150714,11.20353605,11.85550761,12.49142746,13.10652483\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.669945349,8.483893287,9.286344517,10.07251404,10.83753555,11.57700507,12.28732064\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.338062197,10.16604331,10.95962666,11.71661869,12.43573819,13.11642056,13.75869998\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.7098385,8.523794772,9.326256031,10.11243896,10.87747663,11.61696384,12.32729744\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.801535962,8.615061265,9.417289253,10.20336379,10.96836144,11.70783885,12.41816953\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.38754745,10.04880651,10.71599794,11.38060876,12.03490112,12.67241036,13.28812382\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.195489502,9.855637893,10.5201471,11.18161373,11.83307919,12.4685632,13.0833018\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.079696865,7.885489811,8.67927138,9.454954526,10.20811214,10.93548778,11.63471673\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.793960344,8.607526572,9.409788507,10.19589161,10.96091369,11.70041232,12.41076172\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.319549468,9.980298948,10.6472584,11.31182532,11.96619766,12.60386377,13.21977691\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.692285234,8.506122266,9.308491803,10.0946028,10.85958302,11.59902356,12.30931864\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.006488199,7.775765378,8.540822684,9.296135928,10.03689589,10.75887513,11.45845824\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.039991495,9.701044922,10.36627891,11.02833522,11.68028649,12.31617485,12.93125281\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.08893532,7.894896244,8.688801609,9.464575863,10.21780066,10.94522619,11.64449282\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.324582866,10.15255065,10.9461283,11.70311976,12.42224207,13.10292945,13.74521522\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.218510705,9.879215739,10.54428645,11.20629466,11.85825593,12.4941717,13.10926842\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.301279641,9.962032234,10.62899687,11.29356966,11.94794716,12.5856167,13.20153091\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.007478345,7.776678031,8.541689509,9.296971882,10.03770786,10.75966651,11.45923111\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,7.008281922,7.777502818,8.542501243,9.297753651,10.03845272,10.7603732,11.45990157\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.41379717,12.13060697,12.8428945,13.53925571,14.21119699,14.85291201,15.4608404\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.63170361,11.54894375,12.41408089,13.22419041,13.97858709,14.67816848,15.3249033\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.62546817,11.54278555,12.40798072,13.2181327,13.97255897,14.67215937,15.31890454\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,8.771176911,9.465304756,10.15379735,10.83501366,11.50536666,12.16054608,12.79637085\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.43885973,12.15382939,12.8646604,13.5598162,14.23071707,14.87150076,15.47857119\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,8.734429744,9.428958589,10.11776263,10.79922433,11.46977334,12.1251114,12.76106624\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.74610041,11.46556871,12.18578563,12.89511728,13.58425421,14.24637163,14.8769073\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.30342544,11.21761504,12.08006076,12.88778637,13.64007547,14.33779803,14.98289528\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.062365556,9.756945872,10.44597245,11.12779633,11.79880434,12.45465947,13.091159\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.42530293,12.14016766,12.85091945,13.5460143,14.21686726,14.85761251,15.46465155\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.73134819,11.45414314,12.17719359,12.88896269,13.58021029,14.2441641,14.87630346\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.41288512,12.12947855,12.84159819,13.53782726,14.209663,14.85129241,15.45915022\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.72489005,11.44444035,12.16471801,12.874096,13.56326914,14.22541538,14.85597436\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.61239416,11.52923459,12.39402871,13.20384053,13.9579756,14.6573244,15.30385034\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.41357549,12.12864288,12.8395519,13.53477085,14.20572313,14.84654872,15.45365322\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.73173033,11.45453735,12.17760404,12.88939126,13.58065723,14.24462858,14.87678402\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.63483197,11.54882542,12.41109381,13.21867124,13.97084268,14.66847553,15.313507\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.39888041,12.1157385,12.82804974,13.52441829,14.19635601,14.83806027,15.44597325\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.74614029,11.46506749,12.18485933,12.89385061,13.58271,14.24459718,14.87493877\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.74031855,11.46324298,12.1863884,12.89822893,13.58953122,14.25352733,14.88569954\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.74131315,11.4641552,12.1872231,12.89898902,13.59021984,14.25414858,14.88625849\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.050234134,9.743434918,10.43117298,11.11176887,11.78160705,12.43635604,13.07181871\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.39961623,12.11606479,12.82805913,13.52417702,14.19591266,14.83745118,15.44522613\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.077916848,9.772571939,10.46164194,11.14349044,11.81451214,12.47037497,13.10687921\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.76288907,11.48184982,12.20166223,12.91066521,13.59953033,14.26141934,14.89176032\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.59650397,11.51032985,12.37246094,13.17992588,13.9320056,14.6295642,15.27453607\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.36786402,11.28174474,12.14392959,12.95144027,13.70355589,14.40114095,15.04613112\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.059403223,9.754020076,10.44306809,11.12490452,11.79592001,12.45177982,13.08828253\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,10.60663278,11.5235746,12.38844688,13.19832026,13.95250463,14.65189343,15.29845211\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.082172163,9.776741924,10.46574141,11.14752847,11.81849505,12.47430787,13.11076677\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,11.44060198,12.15544804,12.86618447,13.56126686,14.23210989,14.87284735,15.4798804\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,9.002950831,9.696195694,10.38396905,11.06459317,11.73445428,12.3892223,13.02470122\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.63058398,16.20910072,16.72239357,17.18292563,17.60003033,17.98073704,18.33037426\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.3246952,16.05083317,16.69715547,17.277218,17.80114788,18.27669714,18.70995046\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,13.21463073,13.76956949,14.26381572,14.70875018,15.1129281,15.4828071,15.82328803\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.64202401,16.33239362,16.94933095,17.50498635,18.00843116,18.46661894,18.88502524\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.47640211,15.30262851,16.04269081,16.70819463,17.30866611,17.85199816,18.34480725\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.37647599,16.09474931,16.73458628,17.30924078,17.82861406,18.30028771,18.73021623\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.33527968,16.0587814,16.70293261,17.28118771,17.80359815,18.27785898,18.71001131\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.45273504,16.15554304,16.77217132,17.31913874,17.80901031,18.25137692,18.65359715\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.62927675,16.32132459,16.93961425,17.49637657,18.00073951,18.45969747,18.87875608\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.58887446,16.28639478,16.90915362,17.46961216,17.97706708,18.43863825,18.85992602\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.38217055,16.09885109,16.73740147,17.31100387,17.82950751,18.30045563,18.72977399\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.46714312,16.17005651,16.78675973,17.33378069,17.82369106,18.26608665,18.66832973\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.44963673,16.15252268,16.76920423,17.31620631,17.80609873,18.24847617,18.6507002\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.44389949,15.27127239,16.01206997,16.67799987,17.27866562,17.82201847,18.31471917\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.46584621,16.16910105,16.78609206,17.33335797,17.82347841,18.26605514,18.66845498\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.49296242,15.31752861,16.05614964,16.72039879,17.31977403,17.86214431,18.35410598\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.41790364,15.24694676,15.98922782,16.65647394,17.25830876,17.80270241,18.29633243\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,13.92417319,14.4861254,14.98605302,15.43565434,15.84371217,16.21685094,16.56009614\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.47207092,15.29881181,16.03930234,16.70516614,17.30594312,17.84953676,18.34257173\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.41625004,15.24592748,15.98873303,16.65641635,17.25861869,17.80332383,18.29721993\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.58086299,16.27927058,16.90273501,17.46376497,17.97168956,18.43365136,18.85526707\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.49131356,15.31616208,16.05501258,16.71945004,17.31898102,17.86148094,18.35355112\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,15.86974722,16.45134719,16.96712687,17.42969253,17.8484805,18.23059556,18.58142249\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Cd], topology \",,,14.45382832,15.28103297,16.02166514,16.68743491,17.28794752,17.83115527,18.32371937\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,19.92332375,20.34598656,20.68798371,20.96783784,21.19923591,21.39241587,21.55512614\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,19.78253383,20.21552998,20.5636133,20.84689187,21.08004027,21.273918,21.43666855\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,20.05322528,20.46513785,20.79800854,21.07007526,21.29479946,21.48223545,21.63998078\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,19.54834029,19.97647183,20.32045754,20.60027972,20.83050209,21.02189113,21.18251393\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,3.239369453,3.894676663,4.572527998,5.256075357,5.932031082,6.590721786,7.225698898\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,3.305670275,3.98084438,4.676256717,5.374660213,6.062638441,6.730592238,7.372278585\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,3.272848757,3.930547803,4.609804975,5.293956552,5.969916114,6.628199662,7.262521819\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,3.265023092,3.935381576,4.627453829,5.323829,6.010882167,6.67880909,7.321186253\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.591105232,7.399871675,8.200150105,8.984088719,9.745938748,10.48155108,11.18802258\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.518728023,7.303580093,8.082712505,8.850698977,9.602914869,10.33529725,11.04435284\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.552675729,7.334923715,8.109484551,8.871262274,9.616105576,10.34043149,11.04116528\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.580568828,7.367873926,8.152754619,8.928364472,9.689044759,10.43000177,11.14725064\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.629481831,8.417292581,9.193887717,9.955597731,10.69828762,11.41795476,12.11114285\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.981990053,7.832096548,8.668821095,9.48573918,10.27764921,11.04042437,11.77096666\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,8.950573596,9.767357804,10.55148491,11.30040193,12.01256594,12.68721822,13.32424431\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.441093823,8.253851849,9.053610039,9.836389159,10.59786794,11.33397763,12.04129936\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.258741011,8.113224407,8.953185504,9.773054227,10.5677686,11.3330505,12.06558757\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,9.032486048,9.87374982,10.68002078,11.44870559,12.17829834,12.86813847,13.51825572\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.740406424,7.549082515,8.351574836,9.139743498,9.907441398,10.65007394,11.36430379\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.580645823,7.359571185,8.13377731,8.897515143,9.6459618,10.37494405,11.0809129\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.320288887,7.107035098,7.891029233,8.665649657,9.425375579,10.16548744,10.88203217\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,6.614241986,7.394519202,8.168640849,8.931185208,9.677749838,10.4045395,11.10829204\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.615337647,8.413514886,9.200496812,9.972240076,10.72430652,11.45248241,12.15319161\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.062420873,7.914051043,8.753647415,9.574212862,10.37007417,11.1367535,11.87091574\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,9.030831602,9.8490515,10.63362555,11.38234116,12.09388479,12.76765502,13.40364662\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.328673871,8.144229038,8.946587856,9.731810604,10.49564091,11.23406719,11.94370896\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,7.219111196,8.062765308,8.89195676,9.70167927,10.48727458,11.24470626,11.97076504\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,9.038921098,9.874187745,10.67419991,11.4367493,12.16059862,12.84525639,13.49084153\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,13.67107906,14.65334955,15.53162306,16.31570446,17.01525859,17.63946527,18.19682152\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,13.55949555,14.11295852,14.60758532,15.05329716,15.45804489,15.82811368,16.16842466\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.14744926,14.99028413,15.74187848,16.41497542,17.01998026,17.565456,18.05853676\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.45433041,15.23467965,15.93132408,16.55593137,17.11834277,17.62673806,18.08789104\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.28277145,15.08010753,15.80574246,16.46518393,17.06417332,17.60829114,18.10277344\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,13.81533251,14.56273994,15.23770254,15.8482056,16.40170528,16.90481722,17.36327001\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.09864236,14.96450637,15.73769352,16.43005892,17.05175196,17.61141594,18.11642157\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,15.00590015,15.71099936,16.3499713,16.93002836,17.45768648,17.9386505,18.37785738\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,13.65674546,14.63852479,15.51536471,16.29769803,16.99557986,17.61839938,18.17474171\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,16.22229157,16.72835914,17.18567932,17.60193209,17.9832792,18.33459094,18.65968255\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.82805069,15.58458548,16.26457971,16.87794424,17.4327456,17.93567032,18.39237024\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.76710341,15.5046099,16.16458091,16.75765091,17.29287589,17.77781146,18.21871644\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.08834086,14.87953092,15.59857022,16.2513631,16.84399832,17.38231308,17.87170265\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.02586017,14.79916784,15.49507288,16.12282714,16.69047702,17.20494322,17.67216695\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.32297256,15.15517152,15.89774045,16.56290047,17.16081884,17.69995965,18.18741282\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology \",,,14.59809716,15.33441468,15.99968298,16.60212896,17.14910139,17.64697216,18.10119801\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,21.51082164,21.69893811,21.84678115,21.96493827,22.06076694,22.13949984,22.20493527\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,21.52627383,21.71187549,21.85776425,21.97437412,22.06895784,22.14667476,22.21127067\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,21.5384275,21.72232676,21.86681027,21.98225851,22.07587737,22.15278775,22.21670477\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,21.51107636,21.69915234,21.84696368,21.96509553,22.06090377,22.13961993,22.20504148\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,21.52642837,21.71200204,21.85786989,21.97446372,22.06903484,22.14674166,22.21132936\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,21.53838262,21.72228639,21.86677414,21.9822262,22.07584843,22.15276176,22.21668135\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,3.365311834,4.052942386,4.757734197,5.462607706,6.154607545,6.824679928,7.467102853\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,3.363448428,4.051426536,4.75653355,5.461681635,6.153914289,6.824180346,7.466762111\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,3.365221218,4.053023515,4.757984631,5.463012728,6.155145767,6.825327461,7.467836044\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,3.365253975,4.052879877,4.757668537,5.462540239,6.154539402,6.824612014,7.467035869\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,3.363301461,4.051268316,4.756367195,5.46151014,6.153740312,6.824006119,7.466589431\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,3.36527811,4.053080034,4.75804019,5.463066862,6.155198134,6.825377825,7.467884262\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,6.850673893,7.64344964,8.434681544,9.217318826,9.985215305,10.73307661,11.45652326\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.865640237,8.672359835,9.469751016,10.25231814,11.01461121,11.75180229,12.46000872\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,9.330236617,10.1445825,10.9277049,11.67665319,12.38957276,13.06547229,13.70406789\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.468551298,8.332395103,9.175579818,9.994595639,10.7860599,11.54690087,12.27460011\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,6.846327134,7.639561873,8.43110216,9.213958877,9.982021988,10.73001861,11.45358211\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.849449871,8.657691038,9.456528725,10.24042453,11.00391377,11.74216917,12.45131646\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,9.313432707,10.12872763,10.91279181,11.66264927,12.3764319,13.0531425,13.6924958\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.45683679,8.32155609,9.165653447,9.985554534,10.77784492,11.53944013,12.26781934\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,6.849225792,7.64185102,8.433069468,9.215758634,9.983731812,10.73167379,11.45519568\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.864985996,8.671635976,9.469074585,10.25175221,11.0141838,11.75151985,12.45986516\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,9.341819562,10.15533641,10.93769572,11.68594841,12.39823504,13.07355787,13.71162682\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.481521789,8.344198012,9.186298774,10.00432799,10.79490433,11.55495129,12.28194276\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,6.850641036,7.643422095,8.434659288,9.21730133,9.985201877,10.73306656,11.45651596\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.865618899,8.672345483,9.469742371,10.2523142,11.01461117,11.75180546,12.4600145\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,9.330155951,10.14450204,10.92762607,11.67657689,12.38949954,13.06540245,13.70400154\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.468596676,8.332432083,9.175609552,9.994619084,10.78607789,11.54691418,12.2746094\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,6.846391349,7.639625795,8.431163777,9.214016962,9.982075913,10.73006816,11.45362733\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.849602072,8.657838561,9.45667254,10.240565,11.0040509,11.74230279,12.45144633\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,9.313030389,10.12834631,10.91243097,11.66230819,12.37610978,13.05283843,13.69220884\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.456577543,8.321321226,9.165439447,9.985358472,10.77766438,11.53927312,12.26766423\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,6.849069384,7.641711629,8.432947729,9.21565375,9.983642305,10.73159793,11.45513171\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.865005032,8.671652531,9.469090967,10.25176937,11.01420202,11.75153905,12.45988515\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,9.341880068,10.15539497,10.93775339,11.68600574,12.39829226,13.07361498,13.71168371\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,7.481523101,8.344211868,9.186321493,10.00435706,10.79493796,11.55498815,12.28198185\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.25681477,16.00043402,16.66840363,17.27105474,17.81657084,18.31160966,18.76172435\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.15216735,15.88465269,16.5486497,17.1511208,17.69846532,18.19639866,18.649972\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.65280712,15.61593186,16.46098758,17.2044014,17.86034201,18.44086987,18.95620879\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.09832496,15.86689087,16.55447345,17.17278617,17.73098504,18.23642499,18.69516767\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.14230886,15.8787923,16.54545334,17.1497196,17.69828264,18.19704508,18.65118043\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.67096553,15.63365391,16.47774841,17.21997334,17.87466404,18.45397061,18.96816178\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.80276318,16.48439296,17.09926439,17.65632929,18.16257572,18.62365114,19.04426583\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.7938468,15.56693003,16.26519477,16.89686598,17.46928622,17.98889908,18.46132964\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.65619153,15.61835852,16.46248947,17.20508582,17.86034021,18.44031202,18.95521269\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.25915853,16.00248098,16.67020504,17.27265047,17.81799255,18.31288288,18.76286996\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.15192822,15.88439336,16.54838484,17.15085936,17.69821259,18.19615758,18.649744\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.65265608,15.61580596,16.46088113,17.20431019,17.86026292,18.44080055,18.95614747\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.09489764,15.86385288,16.55176603,17.17036037,17.72880035,18.23444791,18.69337041\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.14331199,15.87961348,16.5461442,17.15031467,17.69880544,18.1975119,18.65160274\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.66811191,15.63109626,16.4754519,17.21790586,17.87279706,18.4522792,18.96662439\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,15.80501714,16.4864816,17.10118806,17.65809608,18.16419708,18.62513957,19.04563375\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.79379673,15.56685413,16.26510276,16.89676404,17.46917844,17.98878825,18.46121769\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cd], topology nbo\",,,14.65172797,15.61441615,16.4589973,17.20198089,17.85756819,18.43782668,18.95297495\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,20.9129336,21.08035871,21.21166169,21.31640154,21.4012047,21.47077329,21.52851336\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,20.94948215,21.11160567,21.23862097,21.33985937,21.42177539,21.48894116,21.54466384\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,20.80751206,20.98178384,21.12068693,21.23301646,21.32502108,21.40123726,21.46501958\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,20.68207912,20.87793418,21.03329769,21.15844776,21.26062687,21.34505244,21.41555591\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,3.667496543,4.352654407,5.053050518,5.751946653,6.436629166,7.098245535,7.731255376\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,3.42887349,4.082390961,4.75832711,5.439756688,6.113333643,6.769384765,7.401515044\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,3.295729915,3.954904324,4.640374075,5.333577706,6.019873699,6.688662865,7.332947407\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,3.402283178,4.067468999,4.755250884,5.447861781,6.131454502,6.796118604,7.435404872\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,3.320344694,3.966917617,4.638795587,5.31864152,5.992653536,6.650736449,7.286137512\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,3.223127068,3.876903544,4.559254735,5.25129363,5.937990691,6.608378626,7.255146544\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.190671164,8.014683097,8.833884692,9.639834227,10.42576933,11.18631117,11.91734634\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.997873984,8.766426938,9.522231561,10.26312389,10.9860053,11.68747135,12.36433232\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,9.404270796,10.19361002,10.96260565,11.70553218,12.41782233,13.0962628,13.73892973\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.524373334,8.351258138,9.163498589,9.956019468,10.72454009,11.46548241,12.17601725\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,9.36251367,10.14192386,10.89876325,11.62885562,12.32873737,12.99590716,13.62884238\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.893429159,8.674696053,9.444233863,10.19877242,10.93450712,11.64764038,12.33481173\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,9.410390523,10.17432809,10.92023021,11.64269564,12.33733828,13.00097272,13.63157598\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.093098915,7.879138391,8.665987179,9.445701352,10.21136977,10.95710046,11.67809331\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.209591293,7.945406597,8.686938659,9.428147787,10.16238081,10.88321458,11.58500688\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.183170907,8.007819994,8.827569479,9.633847906,10.41985793,11.18024512,11.91094912\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.978853379,8.746981112,9.502278421,10.24260792,10.96491532,11.66584171,12.34223491\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,9.419496121,10.19960142,10.95905051,11.69274366,12.39652886,13.06743498,13.70364972\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.498885833,8.326164724,9.137458764,9.928123148,10.69428376,11.43269501,12.14077135\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,9.35386275,10.13323427,10.88960262,11.61900937,12.31814163,12.98459668,13.61691214\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.878185386,8.658105646,9.426484095,10.18001974,10.91490601,11.62735096,12.31399734\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,9.365159529,10.13097443,10.87913187,11.60405354,12.30121539,12.96733443,13.60032482\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.083000831,7.867126653,8.653586187,9.433981947,10.20102078,10.94851081,11.67143071\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,7.191643408,7.943349419,8.7010956,9.457848963,10.2062726,10.93954948,11.65187486\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.41451918,11.2044057,11.97920036,12.73231485,13.45731791,14.14906172,14.80403622\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.51041916,11.3174725,12.11396093,12.88943108,13.63507481,14.34448001,15.01363042\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.60821281,11.41812607,12.21078988,12.97828986,13.71373894,14.41207906,15.07018793\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.42742571,11.18483854,11.93976755,12.6822279,13.40301027,14.09481518,14.75253849\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.51820054,11.36499089,12.19004967,12.98514207,13.74343536,14.46019545,15.13277694\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.47243809,11.29342112,12.10205103,12.88787693,13.64216099,14.35862019,15.03340484\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.60663689,11.40841329,12.19401525,12.95557183,13.6861774,14.38070354,15.03592442\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,10.53491814,11.29410125,12.05226175,12.79797867,13.52127999,14.2145461,14.8726175\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,15.478668,16.19115878,16.83429681,17.41627127,17.94404217,18.4235238,18.85978804\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,16.08242874,16.71710415,17.29139321,17.81322162,18.28888662,18.72346939,19.12116928\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,15.69486535,16.39536923,17.02329063,17.58892227,18.10044757,18.56446651,18.98640371\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,15.78621261,16.4878089,17.1157118,17.6804981,18.19053792,18.65257342,19.07214774\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,17.18253398,18.14586736,18.94932429,19.62178327,20.18740313,20.66587927,21.07307448\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,15.56155347,16.24518479,16.86265311,17.42200499,17.93013412,18.392858,18.81509015\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,16.01473109,16.67704416,17.27686631,17.82159544,18.31723476,18.76879136,19.1805612\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,15.94241279,16.61091022,17.21188425,17.75466797,18.24670974,18.69403546,19.10161267\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,15.80391609,16.51146988,17.14617894,17.71769956,18.23386815,18.70115613,19.12500788\n\"linker [O-]C(=O)c1cc(cc(c1)C1=NN=N[N]1)C(=O)[O-], nodes [Cd], [O], topology \",,,17.09765089,18.07109065,18.8831787,19.56301565,20.13495683,20.6188666,21.03075046\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,21.01429249,21.37332973,21.65925918,21.89022138,22.07918092,22.23556473,22.36633902\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,20.5849588,20.99738473,21.32884062,21.59854438,21.82049825,22.00505435,22.15997129\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,21.01665348,21.37542644,21.66111851,21.89187288,22.08065242,22.23688089,22.36752107\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,20.58824581,21.00011879,21.33115155,21.6005239,21.82221313,22.00655443,22.16129458\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.204854659,4.034710437,4.879201091,5.711330737,6.512816823,7.272673818,7.985453645\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.419250084,4.099847056,4.800492074,5.503289157,6.194515231,6.864509523,7.507117046\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.491325686,4.183293087,4.892296573,5.600715983,6.295249663,6.966697982,7.609344695\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.570216502,4.267398974,4.978937635,5.687774216,6.381129981,7.050242615,7.68973909\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.334725812,4.025090435,4.733811541,5.443289752,6.140067856,6.814695768,7.461176914\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.443289673,4.093257283,4.766582356,5.446277108,6.118815729,6.774311768,7.406171481\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.366271744,4.028487687,4.710579919,5.395992201,6.071897948,6.729103129,7.361585341\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.201722082,4.031271,4.875560824,5.707585031,6.509045389,7.268940264,7.981807242\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.419058724,4.099661228,4.800310637,5.503111561,6.194341336,6.86433943,7.506950975\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.491511951,4.183452812,4.892429758,5.600824175,6.295335244,6.96676368,7.609393269\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.570123221,4.267277622,4.978791938,5.687609015,6.380950206,7.050052753,7.689542959\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.334176445,4.024557748,4.733301481,5.442805586,6.139611024,6.814266487,7.460774606\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.442782163,4.09270316,4.765994086,5.445665395,6.118189865,6.773679711,7.40553989\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,3.366202361,4.028428694,4.710536807,5.395966917,6.071890377,6.729112024,7.361608909\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.581049186,8.3885587,9.18026905,9.953312856,10.70450366,11.43068773,12.12907619\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.256020867,10.05189682,10.82287046,11.56488669,12.27469818,12.95006421,13.58972817\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.720221221,8.5122394,9.288753536,10.04746362,10.78549533,11.49983065,12.18770144\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.377206294,10.15081788,10.90089798,11.62422105,12.31781546,12.97941292,13.60757598\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.561111244,8.398824119,9.210825434,9.996741801,10.75546945,11.48546188,12.18511771\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.361618757,10.14564383,10.90299594,11.63119156,12.32788222,12.99129629,13.62037665\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,6.517289691,7.328316152,8.133087947,8.925729233,9.701180985,10.45503075,11.18355418\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,6.607155891,7.398097652,8.184371956,8.959764724,9.719239638,10.45851757,11.17399475\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.359989076,8.186376774,8.997089364,9.789083292,10.55885271,11.3028926,12.01811166\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.705435026,8.521731145,9.326244141,10.11353579,10.87858049,11.61707352,12.32562017\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.01430149,9.839281767,10.63243158,11.39062364,12.11199129,12.795624,13.44135501\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.987756553,8.735949486,9.47531871,10.2032243,10.91601686,11.60978921,12.28092783\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.530115014,10.30590543,11.05448162,11.77301203,12.45944849,13.11245819,13.73136404\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.633827472,10.42059268,11.17450225,11.89454269,12.5800274,13.23056964,13.84611822\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,6.757740852,7.519187294,8.282450267,9.040549595,9.787398463,10.51766899,11.22683803\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.580451316,8.387918716,9.1795984,9.952621855,10.70380126,11.42998151,12.12837238\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.25589806,10.05182096,10.82283556,11.56488739,12.27472953,12.95012163,13.58980745\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.721373253,8.513294914,9.289726538,10.04836682,10.78633937,11.50062406,12.18845089\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.376920188,10.15045824,10.90049392,11.62379374,12.31737986,12.97897937,13.60715142\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.562142593,8.399690499,9.211552497,9.9973528,10.75598452,11.48589794,12.18548875\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.361125677,10.14513955,10.90248169,11.63067036,12.32735776,12.99077228,13.61985646\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,6.5181329,7.328824955,8.133346005,8.925802591,9.701121104,10.45487718,11.18333688\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,6.606372362,7.397502099,8.183925783,8.959439551,9.719013469,10.45837271,11.17391663\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.358961454,8.18531929,8.996041705,9.788070205,10.55788888,11.3019859,12.01726537\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.705715664,8.522066128,9.326631589,10.11397047,10.87905524,11.61758041,12.32615126\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.012858072,9.837896336,10.63111028,11.3893681,12.11080083,12.79449673,13.44028841\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.987046932,8.735187972,9.474521771,10.20240304,10.91517974,11.60894326,12.28007914\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.528835918,10.30454229,11.05308424,11.77161256,12.45806779,13.11110975,13.73005638\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,9.633057979,10.41975927,11.17365209,11.89370428,12.57921744,13.22979731,13.84538791\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,6.759435275,7.520382055,8.28327473,9.041101203,9.787750652,10.51787692,11.22694292\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.605719173,8.39438477,9.172169872,9.933858524,10.67515232,11.39244856,12.08281887\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,7.603503605,8.391979228,9.169707579,9.931425799,10.67280309,11.3902145,12.08071653\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.17964241,15.08559963,15.88666242,16.59870609,17.23441289,17.80405455,18.31608195\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.73676715,15.50340864,16.19164927,16.81165566,17.37207666,17.88019017,18.34211236\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.82437064,15.56986527,16.24794731,16.86453736,17.42545025,17.93610783,18.401443\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.7520786,15.50602733,16.18801497,16.80581503,17.36646811,17.87618784,18.34039986\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,15.30356746,15.98275567,16.59411072,17.14837476,17.65350975,18.1155833,18.53936957\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,15.78658592,16.400168,16.96172684,17.47747059,17.9521751,18.3896607,18.79311498\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.09460462,14.95195274,15.72225854,16.41533188,17.03999189,17.60401391,18.11419803\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,16.07470989,16.71394404,17.28759561,17.80602236,18.27694882,18.70632128,19.09886603\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,12.13795709,13.10490487,13.99432343,14.80938199,15.55420465,16.23348042,16.85216156\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,17.09351655,18.00546369,18.75946657,19.38745024,19.91445872,20.36006812,20.73961409\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.19419623,15.09886844,15.89883125,16.60991479,17.24477148,17.8136527,18.32499492\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.74982513,15.51529665,16.20245602,16.82148076,17.38101964,17.8883449,18.34956454\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.79647305,15.54535719,16.22625654,16.845215,17.40813786,17.9205153,18.38733286\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.754179,15.50790235,16.18967601,16.80728358,17.36776833,17.87734298,18.34143077\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,15.30366779,15.98271134,16.59399828,17.14823944,17.65337748,18.11546808,18.53927814\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,15.82845711,16.43612231,16.99295333,17.50485424,17.9763897,18.41122918,18.81244989\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,14.10968101,14.96520422,15.73398465,16.42577018,17.04933361,17.61241496,18.12178686\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,16.08105042,16.71955721,17.29263951,17.81060951,18.2811604,18.71021679,19.10248991\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,12.1655269,13.12950228,14.01637148,14.82923164,15.57214834,16.24976321,16.86699006\n\"linker O=N(=O)c1cc(ccc1Oc1cc(cc(c1)C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Co][OH]1[Co][OH]([Co]1)[Co], topology \",,,17.08102318,17.9946149,18.74998537,19.37911084,19.90707793,20.35349725,20.7337321\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,19.36383502,19.91022809,20.34973342,20.7074869,21.00195695,21.24685103,21.45245858\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,20.63861635,20.99870546,21.28492787,21.51568293,21.70412626,21.85981662,21.98980782\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,19.15039731,19.71586414,20.17233347,20.5450169,20.85256188,21.1088881,21.32449612\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,19.18323223,19.7670889,20.23363492,20.61133771,20.92083117,21.17725701,21.39187302\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.598390418,4.971391976,5.388011431,5.83883807,6.31348972,6.80220483,7.296657891\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.66186044,5.083566634,5.542759752,6.029449081,6.533288412,7.044988388,7.556952356\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.385436457,4.831013565,5.311950475,5.819078581,6.34228835,6.872243993,7.401202276\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.736946797,5.114334014,5.537352933,5.995147278,6.476410374,6.970872882,7.470001767\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,2.547976552,3.100015833,3.706348479,4.350654382,5.018412022,5.697637645,6.378913224\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.781867139,5.167899425,5.598102552,6.061744463,6.547594983,7.045456065,7.546876742\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.698227624,5.056497706,5.460917493,5.90120505,6.366536942,6.846937132,7.333972361\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.650022408,5.028791171,5.45103133,5.906803714,6.385482842,6.877254055,7.373852741\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.421068616,4.83211493,5.283337481,5.765129246,6.267004393,6.779241789,7.293688233\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.109939879,4.760538049,5.447066615,6.154701015,6.870806208,7.585416396,8.291027401\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.61857885,5.018751188,5.460586091,5.93403743,6.428358398,6.933688465,7.441810825\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,4.643977673,5.024381639,5.447662303,5.904054448,6.383054182,6.874934473,7.371494658\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.81516646,10.2973406,10.794534,11.30509894,11.82456584,12.34733941,12.86776973\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.769453943,10.30390968,10.84843463,11.39974408,11.95282313,12.50226013,13.04301181\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.701047112,10.20007,10.71346379,11.23880626,11.77128092,12.30521859,12.83505492\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.939518747,10.40173727,10.8858814,11.38788916,11.90165685,12.42050274,12.93806769\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,10.8876764,11.50549158,12.07825851,12.61763517,13.13115421,13.62333308,14.09662196\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.858544162,10.33617617,10.83311598,11.34571571,11.86825701,12.39439447,12.91805048\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.932164515,10.39131338,10.87158347,11.36943821,11.87914501,12.39425812,12.90854927\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.888461897,10.36044384,10.84898579,11.35166298,11.86365788,12.37926906,12.8928582\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,10.06502705,10.5266474,11.00499942,11.49709479,11.99795143,12.50195513,13.00368237\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.256004214,9.883929282,10.49263568,11.08437365,11.65964567,12.21797556,12.75842085\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.887480934,10.38349274,10.8927463,11.4132828,11.94058022,12.4691638,12.99360159\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,9.857245225,10.34150366,10.84129564,11.35441813,11.8760522,12.40042171,12.92181666\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.76628996,16.35487227,16.87889936,17.35210423,17.78397358,18.18114478,18.54834757\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.22536349,15.90754681,16.51530021,17.06335021,17.56174953,18.01756958,18.43598744\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.06244471,15.77673398,16.40754458,16.97213687,17.48246409,17.94698667,18.37187722\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.70368422,16.24704115,16.74298629,17.20068151,17.62562095,18.021277,18.39005254\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.61864231,16.27508119,16.86093729,17.38971423,17.87058119,18.31001229,18.71281081\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.80903085,16.40608459,16.94257837,17.43033087,17.87732925,18.28912081,18.66971075\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.94795571,16.51773748,17.03019056,17.4969087,17.92545671,18.32094873,18.68701797\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.83999715,16.454171,17.00452048,17.50325343,17.95874535,18.37689575,18.76202343\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,16.02002757,16.5930627,17.10988283,17.58188526,18.01635944,18.418146,18.79063779\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,10.64917918,11.08598098,11.48537839,11.85508939,12.19992564,12.52292818,12.82608927\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.9126687,16.4972026,17.02533548,17.50765756,17.95114369,18.36056554,18.73936947\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.76711667,16.39312174,16.95094647,17.45473499,17.91396383,18.33515657,18.72297941\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.23859203,15.94006226,16.5649588,17.12791916,17.63896794,18.10522594,18.53199074\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,16.62207414,17.16483059,17.64290612,18.07134383,18.46030919,18.81676336,19.14556363\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,10.9368719,11.33457634,11.70212522,12.04534222,12.36767363,12.67116318,12.95707234\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.51315294,16.17491012,16.75731386,17.27784329,17.74848423,18.17758623,18.57110479\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,16.32053509,16.87507123,17.37322804,17.82670543,18.24317796,18.62780286,18.9841832\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.99774579,16.57951086,17.10383626,17.58201912,18.02144022,18.42708946,18.80251483\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.50409799,16.16205802,16.74282744,17.2631252,17.73440727,18.16465863,18.55958871\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.86619905,16.46479742,17.0037519,17.49436845,17.94427066,18.3587615,18.74169535\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.86877173,16.47362935,17.01687474,17.51049328,17.96251869,18.37850854,18.76248128\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,14.84243147,15.57976589,16.23734892,16.82989739,17.36758986,17.85775364,18.30592157\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.67203771,16.29774412,16.86230224,17.37659248,17.84798085,18.28165802,18.68148447\n\"linker [O-]C=O, [O-][C]=O, nodes [Mn], topology dia\",,,15.74045554,16.34117844,16.87789813,17.36360916,17.80721068,18.21491876,18.59120334\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,20.11369372,20.56310653,20.92297909,21.21493477,21.45462037,21.65353137,21.82023559\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,20.02155922,20.48965258,20.8633532,21.16578557,21.41356844,21.6188457,21.79062988\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,20.11274648,20.56234211,20.92234968,21.21440764,21.45417247,21.65314603,21.81990049\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,20.0224202,20.49038375,20.86398052,21.16632888,21.41404303,21.6192635,21.79100027\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.365802246,4.022613305,4.699524704,5.380429478,6.052649042,6.7069791,7.337314314\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.316995346,3.97485262,4.656423358,5.344116398,6.024097747,6.686351712,7.32425385\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.297466626,3.952003356,4.630077382,5.314496113,5.991653593,6.651636047,7.287836384\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.309409913,3.969604262,4.652971796,5.342029095,6.023055154,6.686139092,7.324745894\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.405174383,4.065005157,4.747333422,5.434735597,6.113574272,6.774026605,7.409641164\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.297552952,3.952105198,4.630191894,5.314620477,5.991785186,6.651772532,7.287975754\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.218358091,3.866330037,4.538505541,5.218099625,5.891705727,6.549449739,7.184660359\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.405030999,4.064847168,4.747164437,5.434559138,6.113393488,6.773844164,7.409459245\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.309509981,3.969714557,4.653091412,5.342156926,6.023189933,6.686279465,7.324890497\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.218442366,3.866437319,4.53863123,5.218239191,5.891855045,6.549605245,7.184819081\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.365619477,4.022443151,4.699372168,5.380297507,6.052538871,6.706890666,7.337246653\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,3.316965956,3.974828653,4.65640601,5.344106357,6.024095222,6.686356525,7.324265544\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.346421374,10.16293833,10.94149528,11.68182996,12.38403206,13.04843271,13.67559753\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.547713453,7.329320931,8.108476983,8.878550225,9.634138967,10.37068089,11.08435805\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.526695478,10.30199649,11.0481981,11.76352518,12.44654091,13.09624989,13.71214648\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.939269322,7.827979217,8.697859111,9.543279424,10.35971671,11.14360268,11.89230065\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.496818414,8.303538679,9.098586272,9.878469492,10.63889472,11.37560138,12.08489576\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.526765372,10.30206318,11.04826693,11.76359935,12.44662208,13.09633864,13.71224267\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.225221381,10.03049806,10.80720763,11.55229168,12.26338287,12.93891684,13.57811474\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.596538257,8.399733677,9.193069798,9.972478997,10.73313604,11.47035671,12.18014489\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.596697534,8.39988661,9.193218261,9.972624517,10.73327973,11.47049927,12.18028668\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.80044197,7.546941515,8.296140713,9.041673042,9.777706789,10.4989425,11.2007535\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.398448709,10.21237244,10.98872533,11.72709459,12.42748293,13.09016901,13.71568741\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.791254015,8.549160469,9.298562368,10.03628589,10.75840959,11.4609134,12.14015918\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.22528354,10.03054301,10.80724037,11.55231578,12.26340083,12.93893041,13.57812514\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.398668692,10.21256902,10.98890294,11.72725686,12.42763277,13.0903087,13.71581869\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.828697985,8.592653512,9.345735125,10.08558075,10.80878349,11.51164816,12.19074531\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.32111508,10.12275535,10.89554686,11.63654219,12.34349522,13.01494126,13.65017281\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.321111114,10.12274228,10.89552418,11.63650939,12.34345206,13.01488789,13.65010971\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.939217225,7.827943434,8.697840616,9.543278328,10.35973242,11.14363406,11.89234623\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.458362458,10.23867436,10.98861829,11.70687999,12.3923363,13.04419408,13.66207144\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.990451736,7.887329813,8.7644433,9.61601085,10.43743708,11.22515727,11.97659706\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.34629682,10.16280373,10.94134768,11.6816676,12.38385436,13.04824004,13.67539102\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.538334572,7.336721298,8.1298873,8.911689886,9.677031252,10.42156928,11.14167355\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.800406745,7.546932314,8.296152406,9.041701572,9.777748847,10.49899533,11.20081478\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.791380145,8.549238008,9.298592341,10.03627086,10.75835326,11.4608202,12.14003389\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.547671334,7.329285077,8.108449706,8.878532241,9.634130014,10.37068017,11.08436449\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.538364106,7.336728471,8.129877922,8.911668175,9.677000303,10.4215314,11.14163048\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.600741918,7.401220145,8.194037375,8.973284587,9.734385591,10.47356626,11.18769951\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.828679597,8.592637495,9.345719503,10.08556401,10.80876461,11.51162649,12.19072056\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.990448474,7.887342493,8.764473722,9.616059398,10.43750307,11.22523932,11.97669333\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,7.496732262,8.303440121,9.098472671,9.8783401,10.63875011,11.37544298,12.08472549\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,9.45835484,10.2386725,10.98862518,11.70689759,12.3923656,13.04423528,13.66212411\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,6.600750306,7.401234786,8.194047002,8.973282292,9.734367632,10.47353113,11.18764724\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.42965904,15.23240437,15.95444168,16.6058924,17.19518337,17.72941271,18.21463112\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.33779908,15.14633409,15.87571727,16.53444771,17.13029359,17.67017285,18.16017168\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.3389683,15.1473498,15.87660997,16.53524027,17.13100337,17.67081324,18.16075317\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.18113352,14.99073581,15.71734973,16.37179749,16.96323221,17.49934666,17.98661013\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.84219029,15.60017138,16.28114665,16.89508015,17.45034886,17.95398033,18.41189245\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.43045057,15.23313899,15.95511996,16.60651642,17.19575615,17.72993776,18.21511217\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,15.027757,15.77391533,16.44484666,17.05045214,17.59878846,18.09651795,18.54924025\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,15.027689,15.77388576,16.44485296,17.05049005,17.59885317,18.09660464,18.54934446\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,13.78988177,14.69224454,15.49582461,16.21397341,16.85795316,17.43722076,17.95973463\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.03085413,14.87383913,15.62730186,16.30350383,16.91265603,17.46324219,17.96233714\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,13.78783479,14.6904151,15.49418377,16.21249597,16.85661757,17.4360087,17.95863059\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.03132588,14.87427535,15.62770633,16.30387941,16.91300508,17.46356678,17.96263914\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.18290104,14.99227558,15.71869966,16.37298798,16.96428787,17.50028752,17.98745269\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.24530448,15.04201988,15.76731785,16.42671369,17.0260352,17.57095192,18.06675519\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.84096492,15.59917628,16.28032542,16.89439255,17.4497657,17.95348009,18.41145899\n\"linker [O-]C(=O)c1ccc(cc1c1cc(ccc1C(=O)[O-])C(=O)[O-])C(=O)[O-], nodes [Zn], topology nor,\",,,14.24201151,15.03921468,15.76489445,16.42459461,17.02416268,17.56928221,18.06525458\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,19.21493923,19.70446081,20.09747635,20.41690391,20.67948613,20.89760473,21.08053173\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,19.23964797,19.72400128,20.11328405,20.42993961,20.69041304,20.90689333,21.08852391\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,19.44986069,19.90285949,20.26705266,20.56338114,20.80719424,21.00987288,21.17995736\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,19.27058863,19.75168027,20.13796398,20.45195265,20.71009049,20.92453828,21.10440307\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.680885876,4.238030898,4.814680264,5.402547243,5.993240258,6.579377022,7.155108558\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.662281946,4.21932664,4.796254654,5.38465092,5.976022604,6.562911213,7.139412313\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.656897054,4.211720444,4.786699109,5.373456073,5.963505398,6.549372102,7.125121055\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.678586951,4.23633591,4.813691536,5.402241092,5.993508525,6.580057039,7.156004948\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.649903823,4.208035316,4.78594275,5.375173323,5.967220665,6.554622155,7.131473114\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.656155603,4.21338932,4.790385256,5.378772778,5.970095936,6.556922693,7.133365529\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.62107725,4.180652472,4.759943293,5.350527482,5.943927529,6.532705841,7.110977795\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,3.626940425,4.185526993,4.764050145,5.354036737,5.946966771,6.535370127,7.113338255\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.892707124,7.615950197,8.333323615,9.044144133,9.746010635,10.43552607,11.10898375\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,9.072592796,9.942272087,10.78456273,11.59103659,12.35594098,13.07602451,13.75007634\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.942869785,7.655710257,8.364903092,9.069253769,9.76597987,10.45139629,11.12157576\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.883428101,7.604358586,8.320652918,9.031158194,9.733178044,10.42312806,11.09718138\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,9.053343241,9.921648799,10.76310926,11.56921807,12.3341228,13.05447655,13.72898713\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.942022267,7.653678326,8.362037485,9.065857386,9.762291929,10.44759466,11.11778634\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.881569855,7.603693663,8.320488907,9.031078166,9.732933156,10.42257688,11.09625308\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,9.035832703,9.906244968,10.74951468,11.55713693,12.32329494,13.04468703,13.72006425\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.931671622,7.642963629,8.351939988,9.057040968,9.755169803,10.44238354,11.11455424\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.925652026,7.642358305,8.354165095,9.0602818,9.758205507,10.44444207,11.11519337\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,9.058284826,9.92820365,10.77048767,11.57686395,12.34167057,13.06170472,13.73577747\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,6.921001733,7.636571009,8.348440523,9.055438557,9.754754508,10.44265692,11.11517336\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.94715567,14.76088716,15.49414148,16.15735675,16.75888222,17.3056005,17.80333055\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,14.5851503,15.3261174,15.99611807,16.60443539,17.15831918,17.66365396,18.12537645\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.11653815,14.07042777,14.91468782,15.66539648,16.33598943,16.93755562,17.47923574\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.99712317,14.87690332,15.65295627,16.34174863,16.95653575,17.50796694,18.00464857\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,14.0275747,14.81657904,15.53106203,16.17996097,16.77053103,17.30885478,17.80015999\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,14.72607014,15.44906957,16.10386785,16.69931721,17.24228131,17.73831529,18.1920816\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,14.39462504,15.21375833,15.94062741,16.58930276,17.17115136,17.69534829,18.16935166\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.88466859,14.77390684,15.55911005,16.25649579,16.87919703,17.43782248,17.94098794\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.95092117,14.76562863,15.49770395,16.15871006,16.7576551,17.30179495,17.7971474\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,14.80961989,15.52473975,16.17357576,16.76428683,17.30330966,17.79593497,18.24666119\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.77192341,14.67228883,15.46608643,16.17034059,16.79873089,17.36222853,17.86968646\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,14.07311955,14.92380296,15.68069287,16.35701626,16.96382675,17.51028248,18.0039816\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.99815955,14.80288225,15.52845312,16.18512958,16.78110113,17.32311411,17.81687055\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,14.43262674,15.19635228,15.88532029,16.50950507,17.07670543,17.59324763,18.06442767\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.81021353,14.71024405,15.50414713,16.20859037,16.83706614,17.40046243,17.90760936\n\"linker [O-]C(=O)CC(=O)[O-], nodes [Cu], topology pcu\",,,13.49689618,14.41841796,15.23447086,15.96051315,16.60939566,17.19170653,17.71617718\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,19.12395548,19.68520111,20.1456102,20.52652821,20.84433813,21.11165472,21.33824295\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,19.19644416,19.74824802,20.20072971,20.57498904,20.88718812,21.14975474,21.37230007\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.579208257,4.24737323,4.935433127,5.62619855,6.306307488,6.966247115,7.59988942\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.577245955,4.241004029,4.924601529,5.611091428,6.287320103,6.943909971,7.574794671\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.599903072,4.272408849,4.963147393,5.655058434,6.33510648,6.994137314,7.626336492\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.707104773,4.371299881,5.053983715,5.738528848,6.412015856,7.065252427,7.692327209\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.61638738,4.274991057,4.952817315,5.633319156,6.303696196,6.954827815,7.580804236\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.631592739,4.306266469,4.997939454,5.689923062,6.369464803,7.027614539,7.658700717\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.694464363,4.359347298,5.042625019,5.727704657,6.401689208,7.055399485,7.682930885\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.613413237,4.270813394,4.947585504,5.627204589,6.296874868,6.947467767,7.573057838\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.631649686,4.306326674,4.997983387,5.68992417,6.369382303,7.027388956,7.658252564\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.578672623,4.246064064,4.93342663,5.623593622,6.303211975,6.962767209,7.596122928\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.585678625,4.250330699,4.934562992,5.621459168,6.29790249,6.954552334,7.585376102\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,3.599720798,4.271916032,4.962297001,5.653844918,6.3335529,6.992283672,7.624230725\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.926401001,8.708902005,9.47902908,10.23347777,10.96848007,11.68032008,12.36573828\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.395435718,10.16441857,10.91478364,11.64122998,12.33934655,13.00590085,13.63884128\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.824013409,8.601407639,9.36407355,10.1099551,10.83628493,11.54006116,12.21847529\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.495649882,10.25261465,10.992593,11.71006486,12.40041652,13.06023607,13.68731705\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,8.006975692,8.79774565,9.574367613,10.33363613,11.07200172,11.78595899,12.47242839\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.540967621,10.30493747,11.05104309,11.77352803,12.46773193,13.13030493,13.75915699\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.073807005,7.904944072,8.727136839,9.53278005,10.31595966,11.07210654,11.79781891\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,6.963722591,7.738806097,8.508399553,9.267363667,10.01105717,10.7352787,11.43638076\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,12.44690781,13.25769358,13.96456424,14.58547512,15.13596344,15.62892773,16.07480428\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,8.077139101,8.848438579,9.605720699,10.34687108,11.06889309,11.76853007,12.44276334\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.568573618,10.32711886,11.07011229,11.79129384,12.48548953,13.14890037,13.7790794\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.695185302,8.497755786,9.287049205,10.0590853,10.80988974,11.53577844,12.23363105\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.643421011,10.3909226,11.1210044,11.82869388,12.50969674,13.16077006,13.77977969\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,8.009822251,8.800718051,9.578140492,10.33862477,11.07841301,11.79384464,12.48173258\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.557241432,10.32200419,11.06883991,11.79193898,12.48660326,13.1494671,13.77844281\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,6.993874923,7.793652723,8.585537903,9.362737298,10.1199946,10.85320338,11.5592208\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.139110817,7.984910211,8.818188871,9.631212539,10.41831526,11.17541266,11.89968906\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,12.48413512,13.29023136,13.99311816,14.61060445,15.15811711,15.64847401,16.09205235\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,8.069015445,8.841776412,9.600263999,10.34243157,11.06532275,11.76570614,12.44058047\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.54521458,10.3068755,11.052406,11.77568903,12.47164964,13.13655913,13.76802187\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.686047724,8.490177982,9.281078415,10.05465478,10.80687048,11.53401227,12.23295145\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.655628742,10.40162062,11.13044549,11.83708822,12.51721669,13.16755567,13.78594421\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,8.012947451,8.803612084,9.580791409,10.34103502,11.08059405,11.79581296,12.48350694\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.53828886,10.30400699,11.05183983,11.77594788,12.47160687,13.13543053,13.76531622\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,6.99650072,7.797339775,8.590249659,9.368409616,10.12654094,10.86052155,11.56720003\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.141727119,7.986382661,8.818826481,9.631212435,10.41780957,11.17449618,11.89843473\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,12.47536747,13.28243803,13.98621863,14.60450019,15.15270687,15.64366206,16.08775239\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.924763311,8.708101603,9.478947345,10.23395649,10.96936574,11.68148187,12.3670725\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.420850551,10.18932631,10.93920442,11.66513265,12.36268133,13.0286164,13.66089296\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.832336727,8.609388693,9.371738621,10.11729581,10.8432861,11.54671211,12.22477301\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.488119963,10.24671818,10.98804913,11.70663065,12.39788458,13.05843195,13.68609587\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.997449638,8.788876117,9.566019838,10.32571652,11.06444587,11.77872301,12.4654825\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,9.53568673,10.30047448,11.04711538,11.76993164,12.46432635,13.12699843,13.75589365\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,7.082081574,7.912961181,8.734581966,9.539448012,10.32175296,11.07701109,11.80187614\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,6.998912943,7.769048838,8.5342801,9.289384463,10.0296729,10.75090809,11.44940854\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,12.42900183,13.24164839,13.95009753,14.57234611,15.12397209,15.61791009,16.06462672\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,14.48930919,15.38158926,16.175655,16.8835966,17.51591175,18.08170381,18.58888266\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,15.91117456,16.54474903,17.10547569,17.60701555,18.05968135,18.47124217,18.84758119\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,13.8063758,14.71718772,15.53638206,16.27283399,16.93503849,17.5308719,18.06750448\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,15.61237207,16.28334547,16.87951544,17.41412938,17.89710495,18.33597254,18.7365511\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,13.75500199,14.70312207,15.55390296,16.31643298,16.99964781,17.61198757,18.16123037\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,15.73084199,16.3632958,16.92505058,17.42866108,17.88382393,18.29802096,18.67703925\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,14.56366449,15.44211225,16.22839942,16.93234798,17.56289932,18.12813415,18.63531839\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,16.50536373,17.05444015,17.54123739,17.9782212,18.37463588,18.73730402,19.07126259\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,14.00927702,14.93000718,15.75713181,16.49919665,17.16465311,17.76152614,18.2972443\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,15.54833266,16.20364921,16.7846296,17.30447365,17.77341534,18.19937391,18.58848912\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,14.75121943,15.60667455,16.37320586,17.06022078,17.67626396,18.22905526,18.7255433\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,16.54509645,17.0897527,17.57281847,18.00660738,18.40025781,18.76051545,19.09235922\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,14.67491247,15.53974287,16.31111683,17.00025212,17.61692283,18.16964455,18.66585342\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,15.99253816,16.61202368,17.16208517,17.65542438,18.10168523,18.5081651,18.88041082\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,13.9377004,14.84526742,15.65897102,16.38877034,17.04385093,17.63251574,18.16218842\n\"linker [O-]C(=O)c1cc(C#Cc2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Mn], topology sql,dmd\",,,15.81724332,16.46766285,17.0464372,17.5661188,18.03612153,18.46360675,18.85411803\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,20.75374272,21.24921042,21.64136895,21.95645444,22.21305107,22.42456107,22.60081497\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,21.14109411,21.57662498,21.92129467,22.19823884,22.4238104,22.60978733,22.7648024\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,20.73128198,21.23013388,21.6250001,21.94227619,22.20066464,22.41365571,22.5911459\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,21.19243254,21.62024749,21.95873638,22.23067597,22.45215152,22.63474134,22.78692824\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.379172762,4.049289286,4.74386492,5.444174538,6.135605698,6.807719374,7.453748595\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.353899039,4.032073967,4.733027609,5.438146156,6.133049475,6.807550038,7.4551056\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.349602461,4.035177504,4.743239318,5.454773686,6.155187186,6.834222557,7.485363191\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.405813013,5.812750864,6.242772131,6.690875913,7.150767213,7.616196671,8.081702328\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.223716153,5.628575553,6.057480236,6.505432106,6.966069852,7.433019205,7.900656038\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,4.96163013,5.361641185,5.787526956,6.234584769,6.696460271,7.166591177,7.639059949\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.354643456,3.924166459,4.522752059,5.136623525,5.753847739,6.364913353,6.962789568\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.53312086,4.186944467,4.866726774,5.553236473,6.231748721,6.89186297,7.526874062\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.420214039,4.017972635,4.643248704,5.281172159,5.919099904,6.547192666,7.158397563\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.376327823,4.046693359,4.741505149,5.442030148,6.133651832,6.805930551,7.452101006\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.358127071,4.035882175,4.73642716,5.441155433,6.135692531,6.809854694,7.457101624\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.348735851,4.0344705,4.742670084,5.454320617,6.154829936,6.833942794,7.485144989\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.399312944,5.806733047,6.237201904,6.685722525,7.146000991,7.611788052,8.077621834\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.229479615,5.634099798,6.062794183,6.510555215,6.971012696,7.437785568,7.90524519\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,4.956696203,5.356368869,5.782013525,6.22892001,6.690723801,7.160851726,7.633375652\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.356676427,3.925750251,4.523952809,5.137506923,5.754474058,6.365335408,6.963052354\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.535702468,4.189229602,4.868772027,5.555081203,6.233421513,6.893385336,7.528262625\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.42483309,4.022253257,4.64723679,5.284904707,5.922606167,6.550495578,7.16151516\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.378899477,4.049034128,4.743592085,5.443857678,6.135227511,6.807270413,7.453225736\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.351539828,4.029969811,4.731156715,5.436477672,6.131551117,6.806192074,7.453862544\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.348049266,4.033800927,4.742031629,5.453719335,6.154267804,6.833419748,7.484659946\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.405778399,5.812723866,6.24275303,6.690864667,7.150763444,7.616199666,8.081711089\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.223126084,5.628006683,6.056936948,6.504916852,6.965583662,7.432562041,7.900227073\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,4.961862687,5.361840921,5.787701011,6.23473836,6.69659752,7.166715531,7.639174405\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.354904708,3.92457064,4.523268678,5.137222198,5.754501505,6.36559989,6.963491259\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.534604352,4.188588247,4.868488151,5.555074811,6.233628396,6.893754375,7.528753526\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.418727298,4.016571994,4.64195366,5.279990739,5.918032463,6.546234819,7.15754229\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.377194275,4.047589689,4.742409935,5.442926789,6.134528088,6.806777867,7.452913803\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.358325004,4.036152304,4.736751709,5.441517183,6.136076597,6.810249085,7.457497166\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.347734227,4.033349738,4.741453254,5.45303244,6.153494009,6.832580083,7.483773205\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.40035487,5.80763836,6.237989879,6.68640923,7.146600257,7.612311953,8.078080947\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,5.228180105,5.632620243,6.061172371,6.508827365,6.969212055,7.435941497,7.903382777\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,4.958514694,5.358207786,5.783876298,6.23080233,6.692616719,7.162744072,7.635255732\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.356403941,3.925564745,4.523846055,5.13747015,5.75449828,6.365411787,6.963172496\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.535689845,4.18929803,4.868899719,5.555251182,6.233620689,6.893603724,7.528492687\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,3.4252487,4.022664157,4.647642962,5.285304409,5.922997128,6.550875643,7.16188259\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.974713195,7.766324487,8.548612767,9.316548739,10.06595395,10.79327866,11.49556805\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.96765639,7.728605326,8.488719517,9.24156357,9.981614982,10.70409075,11.40495196\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.496776538,10.27731602,11.03608378,11.76836443,12.47036256,13.13939391,13.77385272\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.972491307,8.755078945,9.525815974,10.28126908,11.01761058,11.73109623,12.41844759\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.902191977,8.686143829,9.459353263,10.21798646,10.95790685,11.67514326,12.36625753\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.462816464,10.23552098,10.9851229,11.70831343,12.40208601,13.06413872,13.6929919\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.448682838,10.2298065,10.98565322,11.71333435,12.410225,13.07434628,13.7044807\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.3991673,8.256964757,9.090865697,9.898267302,10.67693531,11.42487628,12.14042504\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,12.78425192,13.45286417,14.07978201,14.66697961,15.21584784,15.7277573,16.20427741\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.701363015,8.424919196,9.139962854,9.846920391,10.54376003,11.22712485,11.89325798\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.20788689,7.958890015,8.701506254,9.433814082,10.15303743,10.85589857,11.53906309\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.046816712,7.818790836,8.594868029,9.367727203,10.13013857,10.87555034,11.59846226\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.657837875,10.34632555,11.03022635,11.70297745,12.3587533,12.99280662,13.60157479\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.46735581,11.12053149,11.76542319,12.39734051,13.01184719,13.60521429,14.17459766\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.544489956,10.25243353,10.94941176,11.63086975,12.29243257,12.93037481,13.54183626\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.972498596,7.763045765,8.544570135,9.311997996,10.06110492,10.78829739,11.49058134\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.928160373,7.696569214,8.46258626,9.220057485,9.963715741,10.68899663,11.39204113\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.482420471,10.26374494,11.02295424,11.75544933,12.4575171,13.12653421,13.76093993\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.964030107,8.746708755,9.517368355,10.27264327,11.00875869,11.72200992,12.40914617\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.919453588,8.703740398,9.476746977,10.23482509,10.97396735,11.69029433,12.38043348\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.471827035,10.24287231,10.99093607,11.71268627,12.4051141,13.06592436,13.69364551\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.451313327,10.23309248,10.98946854,11.7175545,12.41473462,13.07904373,13.70928\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.389780978,8.246280437,9.079091918,9.885590859,10.66352458,11.41088444,12.12599201\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,12.7978002,13.4652038,14.09102281,14.67723942,15.22523774,15.73637673,16.2122134\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.687527847,8.412326631,9.128420574,9.836279088,10.53390253,11.21795785,11.88470589\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.198759177,7.949819094,8.692562959,9.425054709,10.14450631,10.84762934,11.53107978\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.072894528,7.843411465,8.618192178,9.389878979,10.15121356,10.89562307,11.61759247\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.661161344,10.348833,11.03216075,11.70450022,12.35997384,12.99380052,13.60239525\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.47227484,11.12357945,11.76708838,12.3979877,13.01174951,13.60457643,14.17357303\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.562364184,10.26812347,10.96336415,11.64341735,12.30382514,12.94080179,13.5514431\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.967757321,7.760558618,8.543735767,9.312331985,10.06222652,10.78991456,11.49247566\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.975302404,7.73460177,8.493218817,9.244722969,9.983591669,10.70503725,11.40501247\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.493912396,10.27420859,11.03251186,11.7641684,12.46544818,13.13372598,13.76744359\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.964437425,8.747371494,9.518319212,10.27387049,11.01023038,11.7236866,12.41098735\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.892559123,8.676597052,9.449790219,10.20831703,10.94807036,11.66511139,12.35603018\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.456024562,10.22862124,10.97801749,11.70093274,12.3943921,13.05612312,13.68467025\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.440497913,10.22207129,10.97833055,11.70637714,12.40358757,13.06798925,13.69837242\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.395617556,8.253091218,9.086551552,9.893435096,10.67154767,11.41893165,12.13395055\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,12.78737855,13.45566119,14.08229907,14.66925591,15.21791526,15.72964227,16.2060021\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.699403291,8.423283261,9.138580472,9.845737685,10.54273603,11.22622843,11.89246539\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.2078086,7.958918845,8.701594593,9.433929893,10.15316021,10.85601589,11.53916798\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.051190743,7.823163925,8.59916149,9.371892691,10.1341478,10.87938823,11.60212244\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.657444143,10.34603523,11.03002301,11.70284405,12.35867456,12.99276984,13.60156987\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.46870479,11.12189589,11.76680518,12.39873409,13.01324325,13.60660321,14.17597059\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.544069938,10.25215021,10.94922806,11.63075995,12.29237823,12.93036238,13.54185558\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.971723829,7.762165609,8.54365649,9.311109709,10.06028667,10.7875802,11.48998426\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,6.926923673,7.695471394,8.461605831,9.219184726,9.962944612,10.68832144,11.3914555\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.481290885,10.26268752,11.02195124,11.75448728,12.45658592,13.12562667,13.76005119\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.962839468,8.745596985,9.51631269,10.27162796,11.00777354,11.72104885,12.40820601\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.916389,8.70090825,9.474125386,10.23239006,10.9716961,11.68816678,12.37843263\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.472396244,10.24342566,10.99147358,11.71320304,12.40560402,13.06638202,13.69406706\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.45274066,10.23441958,10.99070062,11.71869791,12.4157959,13.08002917,13.71019559\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.390025561,8.246353279,9.079019786,9.885396388,10.66322742,11.41050191,12.12553943\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,12.79913919,13.46626653,14.09186838,14.67791266,15.22577337,15.73680198,16.21254982\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.685455205,8.410348598,9.126554176,9.834533865,10.53228209,11.21646134,11.88332929\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.194474845,7.945730766,8.688664952,9.421336853,10.14095747,10.84423905,11.52783881\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,7.074479173,7.844846814,8.619450499,9.390951253,10.15210339,10.89634186,11.61815588\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.659033699,10.34699259,11.03055235,11.70308376,12.35871893,12.9926833,13.60139643\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.47037436,11.12203191,11.76583293,12.39697528,13.01093975,13.60393571,14.1730732\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.563604886,10.26926707,10.96441805,11.64438914,12.30472214,12.94163083,13.55221047\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,8.10994613,8.959576394,9.79224042,10.60309525,11.38731199,12.14068897,12.85998813\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.840188081,10.72011818,11.57053256,12.38612726,13.16247885,13.8965152,14.58658023\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.500228974,10.40205733,11.27129399,12.10289281,12.89300733,13.63915727,14.34017272\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,11.43950744,12.20924335,12.94615532,13.64864478,14.31536424,14.94545789,15.53865295\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.50814493,11.34510643,12.14384591,12.90355187,13.62329155,14.30246397,14.94099833\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,8.120504675,8.969786337,9.802046255,10.61246013,11.39621523,12.1491232,12.86795645\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.818992074,10.7017954,11.55465065,12.37231603,13.15042395,13.88595123,14.577284\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.490287286,10.39293048,11.262912,12.09519729,12.88594476,13.63267646,14.33422438\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,11.47066705,12.23556993,12.96858431,13.6679055,14.33202943,14.95998055,15.55139387\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.5631269,11.39600241,12.19099916,12.94727724,13.66387768,14.34017553,14.97607781\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,8.096349802,8.947020595,9.78061882,10.59231325,11.37728697,12.13134912,12.85127093\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.838311157,10.71828011,11.56872738,12.3843551,13.16074343,13.89482166,14.58493375\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.506714819,10.40786122,11.27648654,12.10754291,12.89717934,13.64290955,14.34355713\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,11.43095848,12.20175409,12.93954656,13.6427702,14.31010585,14.94072085,15.53436084\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.4766454,11.31683924,12.11839777,12.88056249,13.60245096,14.28350684,14.92369774\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,8.122629575,8.97154437,9.803456966,10.61355472,11.39703029,12.14969649,12.86832423\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.821776377,10.70448846,11.55724722,12.37481541,13.15282723,13.88826006,14.57950022\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,9.490130566,10.39274277,11.26268487,12.09493166,12.8856461,13.63235195,14.33388128\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,11.46617967,12.23147989,12.96483834,13.66446198,14.32885458,14.95704612,15.54867572\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,10.55979277,11.39301546,12.18829604,12.94480849,13.66160521,14.33807006,14.97411676\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.45621861,16.15733099,16.77701015,17.33031453,17.82852464,18.28019065,18.69188088\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,13.14419439,14.12504934,15.00498451,15.79504595,16.50523337,17.14447173,17.72067273\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.07121308,15.85858457,16.56351346,17.19691432,17.76778396,18.28361721,18.75073682\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.94866357,16.59607541,17.17489822,17.69677971,18.1703982,18.6023549,18.99778609\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.38199126,16.09316064,16.72131772,17.28180712,17.78613506,18.24303079,18.65920647\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,13.28962864,14.25257696,15.11719347,15.89417611,16.59318797,17.2228542,17.79082941\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,14.9160023,15.7123189,16.42621239,17.06829444,17.64740915,18.17098455,18.64532467\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.74779272,16.41789236,17.01579895,17.55384799,18.04127647,18.48512744,18.89088347\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.38391931,16.09384673,16.7208724,17.28034144,17.78376339,18.2398694,18.65537038\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,13.06469656,14.05269974,14.93921925,15.73525155,16.45080438,17.09483993,17.6753199\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,14.94048937,15.74112458,16.45801939,17.10206785,17.68234079,18.20644818,18.68083992\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,16.06513268,16.6995574,17.26732709,17.77976095,18.24525881,18.67019319,19.05951511\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.37437602,16.08652913,16.71555278,17.2768018,17.7817937,18.23926862,18.65594875\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,13.31345344,14.27393274,15.13640314,15.91152168,16.60891104,17.23716013,17.80389252\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.00478576,15.79347843,16.50031623,17.13597521,17.70929578,18.22766906,18.6973481\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])n1c(C)nnc1c1ncccn1, nodes [Co], topology rna\",,,15.61129675,16.29693077,16.90804929,17.4573838,17.95450105,18.40671467,18.81972771\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,19.8439095,20.3483428,20.75195253,21.07914827,21.34757873,21.57019995,21.75666137\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,19.84736079,20.35124548,20.75442552,21.08127904,21.34943283,21.57182739,21.75810091\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,19.82690366,20.33190114,20.73646391,21.06476606,21.33433441,21.55806109,21.74556306\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,19.82890444,20.33377798,20.73819332,21.06634589,21.33577227,21.5593685,21.74675267\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.559423443,4.268103253,4.992081206,5.712956538,6.4172289,7.095811292,7.743246563\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.611174263,4.340013405,5.081149481,5.815860811,6.530678287,7.216755707,7.86897955\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.559410256,4.268055725,4.991990873,5.712821947,6.417053115,7.095599835,7.743005954\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.609944445,4.338766863,5.079906719,5.814637793,6.529486754,7.215603776,7.867872388\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.559426326,4.26811721,4.992104259,5.712986817,6.417264725,7.095851212,7.743289359\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.611230815,4.340081901,5.081226982,5.815944712,6.530766364,7.216846125,7.869070833\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.559557834,4.268214628,4.992157755,5.712993686,6.417226997,7.095773613,7.743177841\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,3.609921603,4.338740174,5.079877354,5.814606738,6.529454804,7.215571552,7.867840362\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.910680027,7.721829075,8.524020073,9.311099539,10.07810443,10.82098977,11.53654345\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.478838861,9.285472994,10.08093249,10.85921099,11.61458544,12.34219909,13.03833736\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.545082301,10.32659939,11.0838652,11.81247363,12.50933858,13.17243243,13.80062345\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.51561034,10.30578494,11.06876017,11.80101502,12.50011458,13.16449686,13.79335555\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.469506731,9.27061952,10.05985628,10.83227942,11.58267654,12.30636254,12.99960762\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.598581565,7.410607739,8.213743485,9.00246484,9.772290421,10.51941483,11.24064762\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.918022087,7.728501498,8.530037151,9.316489582,10.08290779,10.82525441,11.54032067\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.478949779,9.28566746,10.08119148,10.8595152,11.61491799,12.34254638,13.03868899\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.545259244,10.32681791,11.08411878,11.81275539,12.50964212,13.17275207,13.80095426\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.515755187,10.30595939,11.06894905,11.80120756,12.50030383,13.16467871,13.7935278\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.468042615,9.268894992,10.05790805,10.83015018,11.58041027,12.30400097,12.99718806\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.597678528,7.4097972,8.212980092,9.001714778,9.771530785,10.51863188,11.23983468\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.910672446,7.721807747,8.523988741,9.311060819,10.0780602,10.82094143,11.53649208\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.478827083,9.285447304,10.08089598,10.85916643,11.61453515,12.34214499,13.03828096\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.544962674,10.32650205,11.08378692,11.81241166,12.50929052,13.17239615,13.80059708\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.515494076,10.30568807,11.06868142,11.800953,12.50006773,13.16446351,13.79333401\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.469410236,9.270510187,10.05973503,10.8321483,11.582538,12.30621902,12.99946131\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.598387072,7.410442064,8.213602077,9.002344034,9.772187177,10.51932659,11.24057219\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.918021273,7.728499394,8.530031845,9.316481217,10.08289752,10.82524373,11.54031099\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.47894093,9.285674044,10.0812111,10.85954535,11.6149563,12.34259072,13.03873758\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.545287037,10.32683821,11.08413361,11.81276613,12.50964971,13.17275719,13.8009574\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,9.515731181,10.30593579,11.06892867,11.80119203,12.50029389,13.16467452,13.79352914\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,8.468018337,9.268889921,10.057921,10.83017928,11.58045334,12.30405573,12.99725232\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,6.597714213,7.409835417,8.213020014,9.001755687,9.771572062,10.51867301,11.23987525\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,17.38616748,18.11353968,18.74594409,19.29558773,19.77377877,20.19061766,20.5549183\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,17.38536103,18.11280371,18.74527157,19.29497208,19.77321404,20.19009853,20.55444006\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,17.38598372,18.11336,18.74577071,19.295422,19.77362137,20.19046886,20.55477805\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,17.38556382,18.11298476,18.74543462,19.2951199,19.77334872,20.19022175,20.55455319\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.32599289,14.32492018,15.21641733,16.01311134,16.72596632,17.3645869,17.93743886\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,15.24534458,15.96936737,16.60647875,17.17288413,17.68086298,18.1397641,18.55676763\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.35080417,14.27050778,15.09067957,15.82465326,16.48380651,17.07772917,17.61448283\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,14.49399785,15.29029051,16.00952379,16.66023972,17.24987948,17.78493357,18.27108701\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.36802462,14.36235587,15.24987363,16.04312388,16.75299327,17.38901773,17.95960421\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,15.2600157,15.98252916,16.61839287,17.18374682,17.69082451,18.14894218,18.56525653\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.35245669,14.27202133,15.09201844,15.82580456,16.48477207,17.07851964,17.6151136\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,14.49252179,15.28776559,16.00639895,16.65680131,17.24631018,17.7813494,18.26756068\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.32814419,14.32685072,15.21815317,16.01467626,16.7273814,17.36587051,17.93860691\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,15.24571254,15.96966127,16.60671422,17.17307311,17.6810147,18.13988575,18.55686488\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.35078768,14.27050467,15.09068663,15.82466801,16.48382703,17.07775395,17.61451069\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,14.49205394,15.28866519,16.00814303,16.65905083,17.24884406,17.78402302,18.27027956\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.36664242,14.36110041,15.24872174,16.04205886,16.75200299,17.38809318,17.9587385\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,15.2588508,15.98153856,16.61754937,17.18302788,17.69021137,18.1484191,18.56481023\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,13.35215687,14.27175991,15.0917893,15.82560282,16.48459378,17.07836152,17.61497293\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Cu], topology dia,\",,,14.49220649,15.28747048,16.00612143,16.65653929,17.24606205,17.7811139,18.26733682\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,19.92444876,20.33872198,20.6643937,20.92455771,21.13538766,21.30843654,21.4521095\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,20.05205389,20.44682663,20.75695781,21.00458992,21.20519737,21.36981655,21.50646763\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,5.782723612,6.444660482,7.066892467,7.653262569,8.206407104,8.728036196,9.219322319\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.352664507,3.952166652,4.580067989,5.220672544,5.860958772,6.490957804,7.10361041\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.540878504,4.210123455,4.899908071,5.592358143,6.273858458,6.934873486,7.569352826\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.50975624,4.176662076,4.865460317,5.558002585,6.240366205,6.90273764,7.53884128\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.264630614,3.847035074,4.460027246,5.088355974,5.719080792,6.342079368,6.950007872\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.387802647,3.993518968,4.624585444,5.266053212,5.905588503,6.533790752,7.144037202\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.503433733,4.171799987,4.860562707,5.552094753,6.23291026,6.893518835,7.527862261\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.528093289,4.199641129,4.891223352,5.585067194,6.267635387,6.9294481,7.564493496\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.328972381,3.932022656,4.561430991,5.202112465,5.841600524,6.470371582,7.081692502\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,1.917562633,2.400488704,2.944932081,3.533893627,4.150822774,4.781257663,5.413520339\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,5.617871166,6.284114926,6.911544826,7.503518346,8.062421071,8.589832656,9.086853256\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.387364043,3.985522141,4.611018223,5.248553989,5.885446904,6.511984755,7.121284863\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.543909763,4.21258296,4.901785593,5.59368534,6.274691107,6.935278002,7.569397271\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.489536802,4.158178125,4.84893254,5.543489366,6.227806167,6.891990158,7.529719395\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.143051779,3.720702786,4.332620351,4.962801578,5.597510323,6.225912971,6.840088781\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.390137931,3.993491923,4.622353794,5.261838746,5.899656229,6.526429214,7.135541933\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.510055901,4.18039504,4.870953227,5.564011664,6.246046958,6.907567363,7.542534892\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.523170621,4.193563272,4.884170799,5.577242317,6.25924117,6.92067556,7.555515222\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,3.333376708,3.937704368,4.568269426,5.209966498,5.850314956,6.47978374,7.091638788\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,1.936380954,2.422113509,2.969137021,3.560360743,4.179196089,4.81118729,5.444692335\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.292365566,9.994787927,10.69045564,11.37309211,12.03714291,12.67810864,13.2926443\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.642062573,10.37463862,11.08788996,11.77803588,12.44181022,13.07670603,13.68103893\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,7.353690213,8.13374954,8.907720964,9.669941937,10.41519065,11.13884587,11.83706786\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.607875106,10.33743732,11.04689623,11.73311223,12.39321757,13.02492998,13.62666955\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.238746462,9.939180994,10.63216302,11.31197373,11.973404,12.61214974,13.22495815\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.203946684,9.920436115,10.62567035,11.31462268,11.98272211,12.62621511,13.24230291\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.585937212,10.32296064,11.03856196,11.72976387,12.39386976,13.02875792,13.63299087\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,7.419603431,8.19533311,8.965305163,9.723892553,10.46585922,11.18654788,11.88207694\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.612540881,10.3490683,11.0650082,11.7569643,12.42196291,13.05770844,13.66266262\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.23769824,9.954555193,10.66064707,11.35066051,12.01982069,12.66424067,13.28104464\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,6.623562285,7.387475119,8.147358161,8.897744034,9.633927976,10.35178834,11.04779521\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,7.174852074,8.086717988,9.002109008,9.901877262,10.77193083,11.60275587,12.38860561\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.271816703,9.975478649,10.672316,11.35602172,12.02103586,12.66286742,13.27818553\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.630923424,10.36250601,11.07502568,11.76467691,12.42816016,13.06293434,13.66728331\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,7.35865675,8.138042583,8.911321724,9.67285058,10.41742806,11.14045059,11.83809099\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.606737881,10.33821001,11.04880876,11.73563334,12.39599348,13.02773379,13.62936227\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.246197789,9.945255299,10.63654797,11.3146607,11.97454465,12.61196404,13.22368066\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.233891798,9.947125094,10.64954236,11.33602885,12.00195404,12.64352238,13.25790367\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.583264648,10.32061435,11.03656125,11.72808719,12.39247884,13.0276105,13.63204685\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,7.425152564,8.200144389,8.96936345,9.727194572,10.46842141,11.18840598,11.88328176\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.6241274,10.35864588,11.07283403,11.76326927,12.42695405,13.06157082,13.66556088\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,9.219894839,9.936575212,10.642861,11.33330893,12.00305503,12.64815022,13.26567529\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,6.651323223,7.412302027,8.170787274,8.920948524,9.657735093,10.3767216,11.0741307\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,7.175112775,8.089185222,9.006335236,9.907467448,10.77855048,11.61013044,12.39651531\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,10.34803466,11.13686486,11.89518966,12.62133793,13.31350159,13.97024133,14.59071353\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,10.56539023,11.34288068,12.0903023,12.80606353,13.488372,14.13577776,14.74741795\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,10.41331761,11.1954462,11.94784202,12.6687401,13.35625262,14.00887087,14.6256899\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,10.52225505,11.30183458,12.05127257,12.76898937,13.45319323,14.10242982,14.71583048\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,14.89041729,15.64742071,16.31914454,16.91910285,17.45802971,17.94448102,18.3853357\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,14.81370916,15.55364562,16.21634273,16.81332627,17.35352001,17.8440159,18.29058877\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,16.07529549,16.75313805,17.35623434,17.89532157,18.37868649,18.81304104,19.20402677\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,14.92546316,15.67378651,16.33955682,16.93542441,17.47153482,17.95604138,18.39554663\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,15.30166265,15.97784542,16.58898557,17.14373215,17.64889119,18.10998268,18.53160398\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,15.81088557,16.51879656,17.14743696,17.70831498,18.21037332,18.66086208,19.06585781\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,16.16600179,17.26360637,18.16737253,18.91592421,19.54017873,20.06453195,20.5081455\n\"linker OC(C(C(=O)[O-])O)C(=O)[O-], n1ccc(cc1)c1ccncc1, nodes F[Co], topology \",,,16.02402496,17.1368285,18.05422922,18.81480466,19.4495741,19.98309184,20.43468959\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,19.13777661,19.59794327,19.96397971,20.25929314,20.50062484,20.70014227,20.86682748\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,19.38649905,19.81220722,20.15003878,20.4220887,20.64407519,20.82737392,20.98035397\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.536709349,4.246499548,4.968512679,5.685549308,6.385028838,7.058509366,7.70095114\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.635429979,4.354742429,5.0830961,5.803774475,6.504718912,7.177977536,7.818937333\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.5214339,4.227999438,4.947567392,5.662870968,6.361225737,7.034076118,7.676273964\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.637291707,4.356255226,5.084186803,5.804393372,6.504846246,7.177617948,7.818110987\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.07712325,7.920913156,8.739181534,9.531267785,10.29611615,11.03231211,11.73836257\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.147870658,9.932500171,10.68893571,11.41484936,12.10837456,12.76822248,13.39370862\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.076079162,7.926391579,8.750935219,9.548807478,10.31878628,11.05937031,11.7690462\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.120980636,9.921847189,10.69141539,11.42777443,12.12947871,12.79562437,13.42586322\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.100833616,7.942475053,8.75779524,9.546536424,10.30793331,11.04076935,11.74367716\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.186154173,9.962775482,10.71244253,11.432626,12.12130556,12.77706929,13.39912929\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.052996653,7.897438281,8.717300745,9.511506791,10.27869422,11.01724221,11.72553046\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.132259711,9.927291484,10.69195172,11.42420716,12.12251063,12.78587045,13.41385971\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.363388092,8.15410411,8.940781233,9.717643278,10.47844582,11.21745211,11.92993879\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.009873339,7.740310346,8.473047458,9.203887358,9.927484141,10.63825798,11.33105187\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,6.525672195,7.351029205,8.166247348,8.96530942,9.743458486,10.4968084,11.22223686\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.074951846,7.905148366,8.719910725,9.513882268,10.2829963,11.02408104,11.73472109\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.285131686,8.080646697,8.871522934,9.652022259,10.41600476,11.15784428,11.87291018\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,6.983638547,7.714542973,8.447654109,9.178788932,9.902636293,10.61365243,11.30670908\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,6.503129048,7.327010972,8.139931664,8.936196467,9.711356012,10.46177261,11.18450108\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.109974293,7.939324683,8.75279886,9.54525599,10.31276815,11.0522473,11.76132567\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.764354078,10.5622183,11.35002398,12.11933588,12.86237621,13.57302054,14.24706312\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,10.18631588,10.9714248,11.74131642,12.48928409,13.20910965,13.89590824,14.54637601\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.55776721,10.36119525,11.15167146,11.92231033,12.66636458,13.37832449,14.05429761\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,10.12040618,10.90843514,11.67884334,12.42616683,13.14496394,13.83080232,14.48061462\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.731886993,10.53608069,11.33003621,12.10508933,12.85331295,13.56850806,14.24645315\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,10.29861025,11.08342156,11.85271118,12.59958311,13.31775571,14.00236621,14.650182\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.6106664,10.42219228,11.22005669,11.99697481,12.74601475,13.46164372,14.14005058\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,10.16376509,10.95417766,11.72706754,12.4766381,13.19725088,13.88438521,14.53496108\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,15.08819253,15.77906706,16.40359135,16.97024294,17.48596147,17.9564643,18.38652839\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,14.02996549,14.8875317,15.64667054,16.32259376,16.92755526,17.47143029,17.96223841\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,15.25029256,15.91424197,16.51620544,17.06392152,17.56373791,18.02088657,18.43974002\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,14.08420536,14.93069351,15.68219031,16.35279033,16.95398954,17.49515176,17.98395249\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,13.04621795,14.19256738,15.18543046,16.04796219,16.80019714,17.45898774,18.03835509\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,13.60254423,14.69930393,15.64646205,16.4677851,17.18324398,17.80934402,18.35966776\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,13.02509861,14.17631811,15.17336493,16.03938999,16.79448515,17.45558372,18.0367917\n\"linker [O-]C(=O)c1c(F)cc(cc1F)C1=NN=N[N]1, [O-]C(=O)c1c(F)cc(cc1F)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,13.67306715,14.762664,15.7035693,16.51937794,17.22994663,17.85169884,18.39815287\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,21.07436729,21.50725023,21.85007603,22.12569632,22.35030462,22.53557886,22.69008357\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,21.09684998,21.52650021,21.86669445,22.14015793,22.36298439,22.54677432,22.70003242\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,21.06575007,21.49984224,21.84365659,22.12009072,22.34537433,22.53121347,22.6861945\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.421652411,4.026263105,4.659354453,5.304712296,5.949052886,6.582332228,7.197533636\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.540738098,4.144399902,4.776784164,5.420817469,6.06292851,6.693082776,7.304402331\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.599646594,4.204659179,4.83707791,5.480622791,6.122079115,6.751549264,7.362195632\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.477265576,4.144994348,4.835870256,5.53132047,6.217057456,6.882985343,7.522627219\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.212648998,3.807387873,4.43172,5.070121394,5.709617175,6.340187484,6.954656864\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.17733689,3.767557397,4.386899589,5.020361513,5.655340967,6.282043797,6.89339988\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.601689885,4.270659002,4.959704979,5.651166752,6.331519115,6.991248074,7.624292687\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.420386962,4.02497973,4.658078932,5.303457263,5.947824169,6.58113232,7.19636348\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.535176067,4.138549868,4.770776847,5.414755708,6.056891596,6.687130483,7.298578546\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.596269047,4.201342834,4.833836393,5.477465806,6.119013688,6.74858037,7.359326535\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.473789268,4.141625594,4.83258732,5.528115508,6.213930642,6.879940727,7.519670097\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.21386983,3.808815622,4.433283308,5.071763539,5.711294388,6.341866952,6.956314684\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.176759936,3.766790649,4.385954677,5.019258678,5.654104443,6.280698846,6.891970919\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.601114373,4.27063428,4.960106776,5.651894104,6.332490542,6.992398295,7.625569785\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.421034524,4.025776567,4.659043065,5.304587697,5.949107597,6.582548527,7.197889298\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.535319112,4.138479873,4.770525051,5.414353219,6.056367521,6.686510856,7.297885884\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.59796026,4.20317995,4.835820473,5.479584846,6.121247526,6.750904811,7.361716404\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.474261974,4.142011952,4.832932106,5.528445765,6.214261359,6.880279186,7.520018918\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.214798087,3.809714937,4.434170904,5.072644809,5.712168754,6.342731193,6.957164748\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.174531145,3.764653961,4.383888353,5.01725161,5.652152862,6.278803414,6.890134594\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.601153636,4.27040483,4.959662726,5.651279595,6.331742016,6.991545993,7.62463875\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.421656073,4.026283931,4.659390484,5.304761248,5.949112428,6.582400154,7.197607959\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.54071411,4.144358157,4.776727547,5.420748755,6.062850264,6.692997286,7.304311581\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.599634662,4.204637768,4.8370493,5.480588808,6.122041216,6.751508611,7.362153147\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.477257876,4.14497732,4.835845267,5.531288927,6.2170207,6.882944584,7.522583514\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.212590544,3.807331916,4.43166748,5.070072833,5.709572775,6.340147229,6.954620594\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.177318682,3.767550405,4.386902447,5.02037275,5.655359139,6.282067569,6.893428065\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.601729132,4.270684506,4.959717681,5.651168053,6.331510609,6.991231368,7.624269298\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.420335135,4.024925516,4.658023856,5.303402519,5.94777064,6.581080628,7.196314043\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.535255329,4.138632162,4.770860865,5.414840293,6.056975777,6.687213469,7.298659717\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.596274472,4.201343559,4.833833291,5.477459642,6.119005118,6.748569948,7.359314721\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.473753652,4.141594605,4.83256091,5.528093366,6.213912337,6.879925793,7.519658079\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.213837666,3.808753974,4.433194115,5.071649848,5.711159829,6.341715321,6.956149647\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.176768785,3.766778746,4.38592302,5.019209113,5.654039302,6.280620643,6.891882133\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.601135746,4.270665809,4.960146739,5.651940706,6.332542112,6.992453369,7.625627139\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.42101008,4.025749128,4.659013818,5.304557559,5.949077253,6.582518473,7.197859884\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.535298206,4.138457984,4.770502598,5.414330522,6.056344828,6.686488356,7.297863721\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.597978892,4.20320139,4.835844666,5.479611506,6.121276243,6.750935125,7.361747861\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.474275403,4.142006835,4.832910327,5.528409662,6.214213392,6.880221717,7.519954096\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.214811914,3.809744689,4.434214833,5.072700852,5.712234778,6.342805151,6.957244775\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.174487043,3.764620314,4.383864872,5.017237571,5.65214729,6.27880523,6.890142711\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,3.601161516,4.270392964,4.959633519,5.651235747,6.331686231,6.991480795,7.624566385\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.737362591,10.42675574,11.1114737,11.7844146,12.43959395,13.07231016,13.67913539\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.980352817,10.6194871,11.26717333,11.91359977,12.55021201,13.1701377,13.76823864\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.54508401,10.2484567,10.94896793,11.63863999,12.31064919,12.95963972,13.58174198\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.455929599,8.21835596,8.981506824,9.738912105,10.4841751,11.21147788,11.91592231\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.302931975,8.044536385,8.788142438,9.528415578,10.259651,10.97630159,11.67341592\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.359824563,8.100440068,8.846772565,9.592203443,10.329877,11.05334189,11.75700673\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.58160468,8.357007531,9.124773274,9.880112966,10.61844373,11.33559681,12.0280303\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.860905174,10.59777561,11.31318444,12.00398421,12.66749169,13.30166122,13.90513811\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.563760844,10.28071947,10.98572288,11.67376101,12.34037785,12.98195516,13.59582021\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.481087231,10.20615769,10.91666208,11.60832698,12.27728885,12.92038476,13.53527635\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.825273309,10.56160705,11.27568625,11.96476017,12.62643075,13.25884853,13.86078337\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.745321677,10.43421186,11.1185832,11.79125721,12.44620642,13.07870654,13.6853188\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.996627082,10.63444288,11.28104121,11.9265345,12.56232289,13.18150634,13.77892948\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.548405955,10.25197705,10.95261683,11.64235296,12.31437194,12.96332917,13.58536547\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.457208859,8.220176713,8.983775924,9.741534153,10.48706114,11.21454962,11.91911358\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.294037621,8.037045159,8.78188403,9.523227376,10.2553826,10.97281732,11.67059578\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.349233564,8.090751522,8.837869538,9.583975664,10.32222972,11.04619748,11.75030305\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.574987923,8.351336404,9.119899705,9.875912352,10.61481084,11.33244292,12.02528086\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.851459323,10.58952529,11.30590394,11.99750051,12.66167114,13.29639949,13.90035278\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.556647737,10.27474319,10.98065812,11.66943432,12.33665351,12.9787259,13.59300067\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.483079017,10.20847378,10.91916127,11.61092138,12.27992161,12.92301779,13.53788343\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.805032559,10.54346657,11.25936529,11.9500286,12.61309562,13.24674537,13.84977034\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.74686145,10.43516128,11.11902502,11.79127716,12.44588571,13.07811775,13.68452432\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.997207805,10.63495744,11.28150906,11.92696976,12.56273552,13.18190309,13.77931467\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.54651708,10.24994626,10.95049597,11.64018349,12.31218694,12.96115458,13.58322119\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.452155929,8.215140798,8.978766267,9.736571389,10.48216956,11.20975267,11.91443154\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.291140184,8.034036764,8.778780713,9.520053484,10.25216578,10.96958502,11.66737313\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.353822208,8.095459519,8.842633215,9.588749646,10.32697935,11.05089501,11.75492583\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.578469958,8.354580534,9.122941202,9.878776723,10.61751732,11.33500648,12.02771343\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.858398881,10.59626726,11.31251274,12.00399061,12.66803181,13.30261013,13.90639155\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.56508297,10.28175728,10.98659242,11.67453206,12.34109153,12.98263505,13.59647928\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.469001392,10.1948215,10.90600926,11.59830583,12.26785612,12.91150223,13.52690899\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.811074961,10.54949401,11.26539069,11.95602529,12.61902121,13.25255588,13.85542745\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.737250021,10.42666214,11.1113969,11.78435253,12.43954464,13.07227183,13.67910641\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.980505357,10.61961992,11.26729053,11.91370436,12.55030625,13.17022329,13.76831689\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.545266857,10.24861377,10.94910237,11.6387545,12.31074621,12.95972144,13.58181039\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.455984554,8.218409808,8.981559905,9.738964577,10.48422699,11.21152911,11.91597277\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.302918714,8.044531453,8.788144599,9.528423657,10.25966391,10.97631833,11.67343563\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.359786363,8.100407666,8.846744913,9.592179799,10.32985679,11.05332463,11.75699202\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.581570235,8.356974472,9.124741577,9.880082642,10.61841479,11.33556925,12.0280041\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.860955767,10.59781697,11.31321902,12.00401375,12.66751739,13.30168394,13.90515846\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.563820325,10.28077604,10.98577666,11.67381202,12.34042611,12.9820007,13.59586308\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.481025165,10.20611296,10.91663234,11.60830997,12.27728247,12.92038715,13.53528587\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.825358332,10.56167952,11.27574759,11.96481176,12.62647383,13.25888424,13.86081274\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.745302326,10.43418843,11.11855608,11.79122693,12.44617356,13.07867167,13.68528246\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.99659488,10.63440995,11.28100874,11.92650329,12.56229343,13.1814789,13.77890417\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.548526521,10.25208236,10.95270803,11.6424314,12.31443903,12.96338629,13.58541391\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.457226232,8.220196906,8.983799062,9.741560157,10.48708978,11.21458056,11.91914644\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.294063013,8.037067908,8.781905008,9.523247269,10.2554019,10.97283635,11.67061473\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.349422157,8.090915465,8.838012639,9.584101268,10.32234066,11.04629613,11.75039134\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.574945145,8.351287576,9.119846622,9.875856419,10.61475317,11.3323844,12.02522219\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.851488301,10.58956862,11.30595952,11.99756609,12.66174452,13.29647867,13.90043601\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.556687471,10.27475566,10.98064878,11.66940765,12.33661321,12.97867507,13.59294191\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.483143106,10.20851217,10.9191797,11.61092435,12.27991268,12.92299982,13.53785868\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.805094012,10.54353622,11.25944125,11.95010909,12.61317903,13.24683031,13.8498557\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.746959395,10.43525291,11.11911078,11.79135732,12.44596048,13.07818738,13.68458906\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.997233918,10.63498191,11.28153334,11.92699465,12.56276141,13.18193007,13.77934265\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.546617462,10.25004113,10.95058515,11.64026695,12.31226474,12.9612269,13.58328831\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.452214958,8.215194619,8.97881539,9.736616213,10.48221043,11.20978991,11.91446547\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.291156866,8.034057187,8.778803557,9.520077729,10.25219065,10.96960992,11.66739765\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.353947681,8.095573729,8.842737183,9.588844441,10.32706599,11.05097441,11.75499882\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,7.578464498,8.354574897,9.122936376,9.87877332,10.61751566,11.33500666,12.02771542\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.858490356,10.59633773,11.31256594,12.00402965,12.66805925,13.3026281,13.90640183\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.565050719,10.28174082,10.98658905,11.6745393,12.34110722,12.98265735,13.59650661\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.468978201,10.19480756,10.90600277,11.59830523,12.26786009,12.9115097,13.52691908\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.81125748,10.54965076,11.26552586,11.95614231,12.61912289,13.25264456,13.85550507\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.27718256,12.05199442,12.79266594,13.49841635,14.16835025,14.80183035,15.39866332\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.90425466,12.6293803,13.32411873,13.98705508,14.6171801,15.21387377,15.77693696\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.322615065,10.18965289,11.03215561,11.84570112,12.6257094,13.36836907,14.07104452\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.6581683,11.49367378,12.30151811,13.07696779,13.81571354,14.51458368,15.17174432\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.68541521,11.50894317,12.306895,13.07334121,13.80361282,14.49454465,15.14442416\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.66358371,11.4432395,12.19664783,12.92099979,13.61351435,14.27198595,14.89500207\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.26826081,12.04319352,12.78412537,13.49021823,14.16053828,14.79442282,15.39166204\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.92084085,12.64533896,13.33946008,14.00176664,14.63124699,15.22728739,15.78969763\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.312927465,10.18124123,11.02487053,11.83938929,12.62022865,13.363594,14.06686748\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.67580905,11.50988952,12.31652516,13.09090957,13.82869343,14.5266831,15.18303232\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.66893194,11.49376202,12.29286826,13.06034723,13.79154973,14.48332554,15.13397353\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.61365252,11.39876618,12.15684938,12.88522151,13.58120998,14.24269882,14.86834884\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.2700223,12.0449073,12.78572951,13.49167994,14.16184462,14.79557361,15.39266474\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.92017161,12.64372012,13.33714882,13.99896998,14.62812771,15.22397086,15.78627858\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.287961808,10.15826792,11.00365261,11.8197366,12.60198476,13.34662685,14.05106308\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.63334225,11.4713246,12.28133604,13.05868175,13.79908955,14.49942092,15.15787069\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.67622961,11.50012244,12.29844175,13.06525566,13.79589323,14.48718704,15.13742206\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.69982561,11.47895256,12.23170219,12.95524172,13.64679933,14.30419522,14.92604847\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.2773622,12.05216322,12.79282509,13.49856679,14.16849273,14.80196545,15.39879154\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.90414136,12.62926872,13.32400962,13.98694897,14.61707738,15.21377469,15.77684167\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.322757067,10.18977345,11.03225671,11.84578517,12.62577887,13.36842623,14.07109139\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.6573669,11.49296483,12.30088898,13.07640767,13.81521315,14.51413507,15.17134068\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.68534002,11.50888701,12.30685426,13.07331285,13.80359429,14.49453386,15.14441942\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.66401555,11.44363268,12.19700765,12.92133054,13.61381958,14.27226856,14.89526449\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.26815661,12.04309622,12.78403465,13.49013373,14.16045962,14.79434958,15.39159383\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.9207433,12.6452654,13.33940533,14.00172661,14.63121849,15.22726792,15.78968519\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.313363482,10.18160803,11.02517511,11.83963912,12.62043116,13.36375613,14.06699554\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.6758423,11.50991182,12.31653711,13.09091197,13.82868731,14.52666959,15.18301259\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.66890102,11.49373688,12.29284797,13.06033105,13.79153703,14.48331576,15.13396621\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.61450011,11.39953987,12.15755783,12.88587181,13.58180813,14.24324998,14.86885754\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.27007691,12.04495084,12.78576386,13.49170662,14.1618649,14.79558855,15.39267523\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,11.92019952,12.64374462,13.33717121,13.99899101,14.6281478,15.22399022,15.7862973\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,9.288213266,10.15846693,11.00380295,11.81984354,12.60205411,13.34666442,14.05107427\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.63298684,11.47101191,12.28105745,13.05843064,13.79886088,14.4992109,15.15767645\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.67623555,11.50013154,12.29845197,13.06526573,13.79590243,14.48719496,15.13742854\n\"linker n1ccc(cc1)C1=NN=C([N]1)c1cnccn1, nodes [Cu], topology pcu\",,,10.69983786,11.47897185,12.23172749,12.95527201,13.64683365,14.30423266,14.92608823\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,21.12836552,21.57295423,21.92492546,22.20787286,22.4384558,22.62866682,22.78729453\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,21.00392262,21.4667168,21.83334452,22.12822587,22.36863042,22.56700546,22.7324822\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,21.00387654,21.46667884,21.83331272,22.12819886,22.3686072,22.5669853,22.73246453\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,21.1282129,21.57282938,21.92482141,22.20778477,22.43838023,22.62860125,22.78723708\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.255431957,3.91677785,4.601348739,5.291795182,5.974443328,6.63937233,7.280006995\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.922449012,5.576689687,6.202626479,6.801194957,7.372884651,7.917769546,8.435737337\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.547316057,4.236859391,4.948351234,5.661957227,6.362866678,7.040885799,7.689666918\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.615408038,4.311350351,5.026556334,5.741693737,6.442472548,7.119159808,7.765783053\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.279414556,3.941189671,4.625856777,5.316128317,5.998388108,6.662766826,7.302733617\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.963184701,5.612763584,6.234078298,6.828309116,7.39605292,7.93741532,8.452276047\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.888260646,4.618976941,5.358574815,6.08889547,6.797170384,7.475212277,8.118453079\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.255424237,3.916769425,4.601339959,5.291786303,5.974434531,6.639363738,7.279998685\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.547233385,4.236782113,4.948279105,5.661889996,6.362804073,7.040827529,7.689612682\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.904399306,4.634265359,5.372884671,6.102178835,6.809436941,7.486507948,8.128843571\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.288290677,3.949180156,4.63315101,5.322896388,6.004766911,6.668858731,7.308610795\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.96332298,5.612898825,6.234208529,6.828433197,7.396170294,7.937525821,8.452379764\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.828276263,5.487255986,6.118674423,6.722953206,7.300273037,7.850534611,8.37353801\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.557366439,4.246315804,4.957034422,5.669795093,6.369857293,7.047068631,7.695102779\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.545749004,4.235314576,4.946858373,5.660543938,6.36155425,7.039688292,7.688591863\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.581978901,5.25115378,5.896227625,6.515739749,7.108656183,7.674136135,8.21155801\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.899689357,4.630013535,5.369140013,6.098939356,6.806670453,7.484167138,8.126875899\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.888244914,4.618959244,5.358556079,6.08887636,6.79715136,7.475193648,8.118435041\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.615458097,4.311394839,5.026596418,5.741730261,6.442506121,7.119190876,7.765811949\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.27942317,3.941201207,4.625871159,5.316145257,5.998407215,6.662787675,7.302755794\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.828348448,5.487327117,6.118744472,6.723022156,7.300340843,7.850601195,8.373603271\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.581870943,5.25104323,5.89611709,6.515630861,7.108549939,7.674033127,8.211458568\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.277329006,3.939408745,4.62437093,5.314932336,5.997476701,6.662131447,7.302361213\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.288264922,3.949157883,4.633132122,5.322880644,6.004753998,6.66884831,7.308602534\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,4.922524898,5.576760065,6.202689536,6.801249881,7.372931312,7.917808259,8.435768677\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.911215473,4.639885727,5.377313158,6.105487796,6.811738198,7.487930792,8.129519805\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.91120445,4.639872311,5.377298447,6.105472591,6.811723062,7.487916103,8.129505804\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.899757447,4.630088426,5.369219517,6.099021678,6.80675414,7.484251044,8.126959135\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.904356005,4.634206932,5.372814833,6.102100713,6.809353123,7.486420544,8.128754265\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.545743145,4.235304988,4.946844997,5.660527092,6.361534443,7.039666097,7.688567847\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.277316358,3.939392955,4.624352215,5.314911061,5.997453303,6.662106377,7.302334904\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,3.557469943,4.246426959,4.957150672,5.669914136,6.369977197,7.047187855,7.69522014\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.180796263,9.843894827,10.50932773,11.17058482,11.82130128,12.45587934,13.06978869\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.852756222,8.651142588,9.438502805,10.21075056,10.96340291,11.69221326,12.39358434\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.859927061,8.656460931,9.442717405,10.21439837,10.96684677,11.69568245,12.39721087\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.413681069,10.07882393,10.74887533,11.41559306,12.07142094,12.71002428,13.32648888\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.192334146,9.852594992,10.51598162,11.17576907,11.82542935,12.45924426,13.07259654\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.406504203,10.23152616,11.02195576,11.7757217,12.49162952,13.1691798,13.80845481\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.343881657,10.17198828,10.96535915,11.72188282,12.44037002,13.12034201,13.76190326\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.180817833,9.843914522,10.50934528,11.17060005,11.82131414,12.45588985,13.06979698\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.445865,8.302815904,9.144484133,9.965082693,10.75972214,11.52442046,12.25615251\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.21336327,9.876588379,10.5423921,11.20398738,11.8548762,12.48941165,13.10306076\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.441309584,8.301814344,9.146970381,9.970861182,10.76849474,11.53582458,12.26979733\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.393578636,10.05778384,10.72732887,11.39391552,12.04992181,12.68894634,13.30601319\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.932405612,7.717868476,8.493700497,9.255362989,9.999055659,10.72148285,11.4198276\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.221404679,8.036784431,8.837317945,9.617170423,10.37224611,11.09965123,11.79738051\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.213490669,9.876700544,10.54249306,11.20407983,11.85496196,12.48949195,13.10313644\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.396149344,10.06423934,10.7365448,11.4049818,12.06213351,12.70177561,13.31907581\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.39711513,10.0615149,10.73098631,11.39727369,12.05281544,12.69127095,13.3077167\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.859925891,8.656461349,9.442716588,10.21439465,10.9668393,11.69567095,12.3971954\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.441284546,8.301788508,9.146944174,9.97083489,10.76846856,11.53579866,12.26977179\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.212670763,9.874656008,10.53931745,11.19991438,11.84996452,12.48381938,13.096935\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.486167675,8.338391642,9.175448878,9.991780108,10.78259535,11.54393666,12.27276155\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.852869611,8.651262717,9.438626856,10.21087636,10.96352877,11.69233789,12.39370677\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.142660468,7.955120844,8.753191551,9.531378816,10.28573022,11.01334885,11.71213526\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.80105135,8.60658995,9.400863016,10.17948884,10.93784622,11.67164988,12.37732291\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.932454902,7.717909471,8.493735033,9.255392341,9.999080748,10.72150437,11.4198461\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.959254224,7.734299323,8.502587341,9.258802034,9.998596481,10.71827917,11.41473988\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.191571093,8.015126826,8.822368452,9.607761909,10.36742572,11.09862606,11.79948286\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.834812566,8.639006089,9.432503636,10.21074744,10.96895219,11.70270173,12.40832604\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.343914935,10.17201268,10.96537562,11.72189221,12.44037313,13.12033964,13.76189618\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.97447106,7.749575036,8.517556242,9.273321512,10.01263911,10.73186892,11.42791732\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.192410876,9.85265677,10.5160305,11.17580679,11.82545747,12.45926418,13.07260948\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.396363261,10.06441863,10.73669712,11.40511279,12.0622474,12.70187562,13.3191644\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.413651502,10.07880356,10.74886328,11.41558826,12.07142229,12.71003077,13.32649956\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.952175427,7.733385871,8.505351337,9.263667807,10.00457758,10.72476601,11.4213622\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.37627973,10.20684205,11.00249936,11.76103216,12.48117558,13.16241289,13.80484341\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.439640841,8.294444651,9.134835703,9.954829311,10.74935141,11.51426615,12.24642886\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.486208833,8.338438815,9.175501822,9.991838255,10.78265794,11.54400284,12.27283045\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.974476502,7.749579355,8.517559913,9.273324801,10.01264215,10.73187177,11.42792001\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.22148203,8.036838918,8.837357012,9.617199571,10.37226937,11.0996715,11.79739981\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.959544171,7.734534074,8.502781385,9.258965031,9.998735129,10.71839829,11.41484305\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.801165343,8.606692288,9.400954383,10.17957005,10.93791815,11.67171346,12.37737902\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,6.95218181,7.733399263,8.505371984,9.263695295,10.00461112,10.72480465,11.42140495\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.191527101,8.015085938,8.822328271,9.607720635,10.3673821,11.09857931,11.79943259\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.445674659,8.30264422,9.144329085,9.964942547,10.75959534,11.52430559,12.25604829\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.397311102,10.06168176,10.73112971,11.39739787,12.05292368,12.69136581,13.30780024\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.185365786,7.999700299,8.799058784,9.578023537,10.33270049,11.06024892,11.75862706\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.376301662,10.20686205,11.00251791,11.76104961,12.48119222,13.16242891,13.80485894\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.142589088,7.955064214,8.753145932,9.531341743,10.28569998,11.01332421,11.71211526\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.393488054,10.05770261,10.72725515,11.39384797,12.04985948,12.68888852,13.30595934\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.834782923,8.638980587,9.432482767,10.21073134,10.96894074,11.70269463,12.40832288\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.406546062,10.23156372,11.02198963,11.77575246,12.49165768,13.16920578,13.80847894\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.385530806,10.21290251,11.00524716,11.76055274,12.47769817,13.15625324,13.79635828\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.185684667,7.999965183,8.799280945,9.578211366,10.33286034,11.06038572,11.75874467\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.385566776,10.21292888,11.00526707,11.76056832,12.47771088,13.15626407,13.79636788\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.212475284,9.874495822,10.53918572,11.19980608,11.84987577,12.48374704,13.0968765\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,7.439574336,8.294380198,9.134772306,9.954766276,10.74928833,11.51420284,12.24636532\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.34901336,12.07032762,12.78507432,13.48294283,14.15606684,14.79896851,15.40823576\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.042183245,9.740392828,10.43216567,11.11606585,11.78867685,12.44582479,13.08343164\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.005988447,9.707215888,10.40130848,11.08698363,11.76097137,12.41922077,13.05774853\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.59138463,11.51778607,12.38993195,13.20549536,13.96421437,14.66728616,15.31689205\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.34933168,12.07059096,12.78529482,13.48312949,14.15622643,14.7991062,15.40835554\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.47823543,11.206049,11.93324719,12.64929948,13.34545299,14.0150973,14.65368753\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.36631036,12.09342239,12.81264494,13.51368233,14.18881958,14.83278251,15.44236587\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.4781351,11.20596775,11.93318127,12.64924595,13.3454095,14.01506195,14.65365882\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.39049672,12.11569613,12.83332871,13.53302864,14.20702187,14.84998716,15.45868347\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.39043276,12.1156397,12.83327818,13.53298291,14.20698016,14.84994891,15.45864824\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.006120918,9.70732589,10.40140067,11.08706156,11.76103777,12.41927774,13.05779774\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.71966385,11.64151678,12.50966032,13.32145914,14.07647124,14.77580493,15.42161183\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.69465388,11.62405983,12.49813504,13.31458447,14.0732298,14.77538687,15.42337217\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.5912806,11.51769046,12.38984367,13.20541346,13.96413803,14.66721471,15.31682494\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.102656953,9.798332736,10.48781418,11.16962939,11.84030906,12.49563104,13.13148115\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.4080723,11.13876452,11.8689232,12.58802149,13.2872721,13.96001659,14.60166282\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.64095458,11.56630367,12.43788151,13.25306697,14.01141031,14.71400286,15.36297695\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.64057067,11.56595632,12.43756155,13.25276848,14.0111295,14.71373727,15.36272495\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.102525731,9.798209996,10.48770032,11.16952436,11.84021251,12.49554246,13.13139995\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.36656602,12.09363253,12.81281897,13.51382732,14.188941,14.83288463,15.44245209\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.3653849,12.08459563,12.79749854,13.49376394,14.16550275,14.80721247,15.41545647\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.46080934,11.18853051,11.91580184,12.63207333,13.32856718,13.99864672,14.6377423\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.08781304,9.783438393,10.47294451,11.15484047,11.82565207,12.48115584,13.11723555\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.40778721,11.13851958,11.86871115,12.5878368,13.2871104,13.95987438,14.60153723\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.39762873,11.13057976,11.86235144,12.58260523,13.28268636,13.95603095,14.59811456\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.71952786,11.64139285,12.50954628,13.32135354,14.076373,14.77571326,15.42152607\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.39754202,11.13049976,11.86227631,12.58253374,13.28261773,13.95596471,14.59805043\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.042310947,9.74050141,10.43225787,11.11614402,11.78874304,12.44588074,13.08347887\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.46091265,11.18861819,11.91587712,12.63213841,13.32862361,13.99869572,14.63778485\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,9.087980464,9.783587691,10.47307827,11.15496087,11.82576094,12.4812547,13.11732568\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,10.69488043,11.62426087,12.49831564,13.31474826,14.07337945,14.7755244,15.42349914\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,11.36540874,12.08462138,12.79752552,13.4937916,14.16553064,14.80724025,15.41548387\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.16111903,15.90070267,16.55354667,17.13573815,17.65925052,18.13314029,18.56437523\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,13.97583478,14.8588618,15.65349486,16.36944801,17.01538966,17.5989949,18.12703782\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.82253953,16.48138437,17.05968407,17.57341752,18.03451721,18.45196343,18.83256688\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.8243402,16.48295983,17.06107365,17.57465255,18.03562273,18.45295952,18.83346977\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.15932892,15.89911927,16.55213972,17.13448207,17.65812389,18.1321252,18.56345671\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.52283381,16.21156772,16.81743905,17.3561411,17.83962525,18.27702548,18.67535904\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,13.54162838,14.46684821,15.29923402,16.04878258,16.7245305,17.33454806,17.88599682\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,14.01806764,14.8888125,15.67523402,16.38560388,17.02767653,17.60854648,18.13461596\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,14.87783257,15.6495408,16.33027723,16.93667756,17.48122774,17.97343638,18.42066037\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,14.87829575,15.649948,16.33063739,16.9369981,17.48151472,17.97369476,18.42089422\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.39692732,16.10756566,16.73720218,17.30053877,17.80851138,18.26940501,18.68961435\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.76468151,16.42300924,17.01039546,17.53908124,18.01827631,18.45501946,18.85478197\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,13.54206263,14.46724524,15.29959678,16.0491142,16.72483404,17.33482636,17.88625248\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.39786292,16.10838384,16.73792182,17.30117535,17.80907757,18.26991121,18.69006913\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,14.01685039,14.88770037,15.67421922,16.38467762,17.0268301,17.60777169,18.1339053\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,14.24382466,15.09753123,15.86771191,16.56290657,17.19098319,17.75905113,18.27346986\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,13.97637723,14.8593056,15.65386426,16.3697603,17.01565734,17.59922715,18.1272415\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.13202631,15.87295672,16.52106584,17.09425017,17.60615283,18.06720655,18.4854267\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.770852,16.42830312,17.01498767,17.54310252,18.02182652,18.4581763,18.85760688\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.13229975,15.87319665,16.5212787,17.09444107,17.6063258,18.06736478,18.48557268\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.52005041,16.20913734,16.81530087,17.3542469,17.83793652,18.2755112,18.67399402\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.44751282,16.15052561,16.76696705,17.31362537,17.80319569,18.24532623,18.64739514\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,15.44624542,16.14938399,16.76592899,17.31267445,17.8023195,18.24451515,18.64664152\n\"linker [O-]C(=O)c1cc(C(=O)Nn2cnnc2)c(cc1C(=O)Nn1cnnc1)C(=O)[O-], nodes [Zn], topology hcb\",,,14.244617,15.09823109,15.8683338,16.56346218,17.19148202,17.759501,18.27387729\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,20.56073806,20.74584674,20.89265187,21.01085592,21.10731638,21.18697879,21.25347541\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,20.59565137,20.7707407,20.91096524,21.02476859,21.11823724,21.19583536,21.26088899\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,20.77781359,20.96488923,21.11332643,21.23287049,21.33043043,21.41099865,21.47824627\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,20.73109961,20.90560288,21.04524154,21.15850131,21.25148236,21.32865005,21.39332643\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,11.27514846,12.15977614,13.00535019,13.80489131,14.55389396,15.2502855,15.89400581\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,11.35055612,12.24201216,13.09112318,13.89158281,14.63954138,15.33349627,15.97385007\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,11.17542545,12.06577385,12.91589679,13.71913045,14.47119942,15.1701913,15.81615605\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,11.285093,12.17812077,13.02854219,13.83008135,14.57891818,15.27358002,15.91449801\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,7.18911584,7.90298534,8.568386857,9.18731563,9.761139217,10.29129789,10.77957867\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,2.505636115,3.141808892,3.813995702,4.5039223,5.197201034,5.883264598,6.55485318\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,7.094259443,7.82063064,8.497261435,9.126087799,9.708552715,10.24622557,10.74103551\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,2.51395997,3.148339476,3.819075985,4.507831786,5.200162394,5.885453121,6.556406156\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,10.94637575,11.75287936,12.4734425,13.1135675,13.68230791,14.18980036,14.64587794\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,9.937157669,10.72365221,11.42380069,12.0439683,12.59379442,13.08375179,13.52382329\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,10.95128364,11.7606367,12.48277427,13.1236935,13.69275275,14.20027758,14.65621862\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,11.08717842,11.88081561,12.5888156,13.21716312,13.77515805,14.27302883,14.72060488\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,13.98185722,14.9254589,15.77094175,16.52878939,17.20824592,17.81760374,18.36436597\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.06412609,15.02760331,15.89364847,16.66957307,17.36333623,17.98300288,18.53638118\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,13.91869014,14.84017384,15.67014966,16.417327,17.08966175,17.69449728,18.23863327\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,15.77764627,16.56485487,17.26378145,17.88394997,18.43406955,18.92215722,19.35553423\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,17.01259464,17.39100643,17.74284421,18.07429818,18.38876446,18.68801887,18.97296651\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,17.02787797,17.40309914,17.74957812,18.07416523,18.38082581,18.67181039,18.94840542\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.40177094,15.35956604,16.21366867,16.97435482,17.65136786,18.2538524,18.79026668\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.28983074,15.26004129,16.12441259,16.89360218,17.57771968,18.18621699,18.72779395\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.29974486,15.16455463,15.94347878,16.64633674,17.28116072,17.85481503,18.37337103\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,15.23599394,16.0220541,16.72634125,17.35772092,17.92389596,18.4318102,18.88780283\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,16.06695032,16.43197311,16.77251166,17.09424112,17.40024531,17.69209022,17.97052657\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,13.99693813,14.31939677,14.62388192,14.91449661,15.19329662,15.46115909,15.71835595\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.71532425,15.55732339,16.31611586,16.99999682,17.61620627,18.17129692,18.67130346\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,13.96012591,14.92134385,15.78576273,16.56048375,17.25333666,17.87230258,18.42513321\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.02596219,14.93265863,15.75193062,16.49124651,17.15772462,17.75813795,18.29889284\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,15.32186648,16.16877045,16.91993922,17.58609092,18.17685753,18.70099226,19.16642181\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,16.8574698,17.26003401,17.63091916,17.97763898,18.30451594,18.61398824,18.90744379\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,16.82584003,17.23232997,17.60363079,17.94821895,18.27121156,18.57569116,18.86355618\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.26377269,15.23707805,16.10416871,16.87580206,17.56210084,18.17251012,18.71572744\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,14.27913004,15.24811073,16.11107335,16.87878611,17.56142564,18.1684845,18.70868664\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,13.88465421,14.79490809,15.61332977,16.35035773,17.01470918,17.61390567,18.15460885\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,15.41005683,16.16169466,16.83741673,17.44501533,17.99128896,18.48244579,18.92423598\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,17.01763422,17.39844106,17.75150241,18.08331952,18.39753935,18.69613198,18.98014911\n\"linker [O]P(=O)(O)[O], [O]P(=O)([O])O, nodes [Cd], topology hcb\",,,16.80494553,17.21440554,17.58851921,17.93582242,18.26144467,18.56845809,18.85874148\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,20.48065044,20.9595866,21.34007951,21.64700145,21.89797693,22.10572074,22.27956466\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,20.11898087,20.64507048,21.06651706,21.40852448,21.68936391,21.92247164,22.1178673\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,20.38576227,20.88050886,21.27438714,21.59247189,21.85268088,22.06803176,22.24813416\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,20.37609752,20.86523957,21.25582814,21.57213979,21.83156985,22.04679051,22.22718104\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,20.15348964,20.67242509,21.08836297,21.42608317,21.70355735,21.93400425,22.12728238\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,20.39947552,20.88581588,21.27440429,21.58918236,21.84736134,22.06151149,22.24095499\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,3.355738514,4.042537347,4.746790307,5.451388731,6.143306267,6.813412048,7.455914927\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,3.394278644,4.082423974,4.787138853,5.491491074,6.182631816,6.851586273,7.492690238\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,3.394002236,4.082336521,4.787082005,5.491393266,6.182485465,6.851431611,7.492603064\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,3.375765177,4.063284793,4.767963555,5.472709225,6.164552617,6.834434919,7.476636853\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,3.386328701,4.077106243,4.784367767,5.491036447,6.184194649,6.854849686,7.497350326\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,3.364023296,4.050064586,4.753459302,5.457168611,6.148236648,6.817593047,7.459493276\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.737393142,8.544739355,9.339546137,10.11793024,10.87558446,11.60841851,12.31297476\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.329331712,8.197250897,9.045375733,9.870008666,10.66750886,11.4345555,12.16842423\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.740225349,8.551025202,9.349410991,10.131265,10.89211996,11.6277878,12.33476288\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,9.32307915,10.14197723,10.92708555,11.67632855,12.38847616,13.06296993,13.69981783\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,9.255829316,10.07956733,10.86870309,11.62133403,12.33638028,13.01340408,13.65250523\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.302071845,8.171933228,9.022061319,9.848625806,10.64790914,11.41655782,12.1518435\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,6.581804924,7.39594009,8.204285499,9.000353346,9.778692702,10.53470321,11.26462138\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.306999023,8.175164293,9.023744592,9.848939955,10.64706267,11.41476993,12.14932518\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,6.639972946,7.457778302,8.268723726,9.066501437,9.845838186,10.60227964,11.3321748\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,9.309344049,10.13223872,10.92028329,11.67163302,12.38526165,13.06077671,13.69831475\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,6.589753387,7.405856278,8.217156247,9.016540252,9.798143657,10.55712073,11.28958355\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.744249448,8.553338678,9.350230061,10.13082513,10.89065329,11.62550833,12.33185878\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,6.615181449,7.434089726,8.246580192,9.045981426,9.826825579,10.58457729,11.31557112\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.29895484,8.168366129,9.017643761,9.84303701,10.64095713,11.40817688,12.14206934\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.717758439,8.528558012,9.327306323,10.1097086,10.87119599,11.60752633,12.31516736\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,9.276947716,10.09918551,10.88677092,11.63781262,12.35126932,13.02674579,13.66437704\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,9.274661351,10.09840365,10.88791653,11.64109296,12.35671207,13.03424814,13.67375234\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.767396533,8.569376737,9.359779856,10.13459938,10.88939762,11.6199582,12.32271005\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,6.598728571,7.415053443,8.226471722,9.02612203,9.808276654,10.56811573,11.30170327\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,9.254377605,10.08229471,10.87433572,11.62894975,12.34531186,13.02317028,13.66276092\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.322997141,8.190489901,9.037380946,9.860245867,10.65569955,11.42062943,12.15246332\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,6.579313222,7.40365185,8.222226707,9.028191869,9.815808647,10.58026475,11.31766123\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.747101246,8.549498509,9.340484195,10.11595366,10.87141832,11.60263852,12.30603427\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,7.302262376,8.164518963,9.007671424,9.82807257,10.62211157,11.38646104,12.11835571\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,14.65474359,15.40817424,16.08826675,16.70417238,17.26359936,17.77302714,18.23792726\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,14.62516818,15.35376026,16.01033127,16.60548236,17.14751695,17.6429992,18.09720099\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,17.33958143,17.92584293,18.43668329,18.89003572,19.2976421,19.66732393,20.00448326\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,17.6618786,18.17919918,18.64061698,19.05862468,19.4408121,19.79198165,20.11540271\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,14.61918221,15.37984057,16.06547312,16.68566451,17.24843086,17.76047681,18.22744185\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,17.94409981,18.36994383,18.76004461,19.12278009,19.46239745,19.78101636,20.07976883\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.73308269,14.75863378,15.66483225,16.4664652,17.1768356,17.80764125,18.36905708\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.50395252,14.34687331,15.10995566,15.80330073,16.43490764,17.01131644,17.53803899\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,18.42505204,18.822234,19.18870103,19.53052599,19.85078104,20.15101661,20.43211428\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,14.87603284,15.64848311,16.34388607,16.9711795,17.53829318,18.05211352,18.51858021\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,18.97007407,19.31068983,19.61880789,19.90439835,20.17266082,20.42612388,20.66592872\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.39509102,14.45865475,15.39871568,16.23017493,16.96663885,17.62018733,18.20139391\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,17.64303874,18.14515941,18.59524629,19.00495832,19.3812623,19.72846905,20.04944901\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,17.93329557,18.35376969,18.73956146,19.09898279,19.43616491,19.75309632,20.05078001\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,18.24773836,18.68126915,19.07521763,19.43817778,19.77492012,20.08817288,20.37965516\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.38291881,14.43470675,15.36359957,16.18530072,16.91374566,17.56104814,18.13765283\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.60640973,14.44510106,15.20762294,15.90209705,16.53530454,17.1131023,17.64066756\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,12.99333996,13.85198574,14.63357258,15.34738898,16.0006627,16.59926386,17.14816349\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.55908655,14.43547255,15.22950803,15.94965877,16.60330217,17.19698068,17.7365576\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,18.98065192,19.33919488,19.66130452,19.95794729,20.23487157,20.49497086,20.73967753\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,18.33117084,18.74755505,19.12863092,19.48174199,19.81082267,20.11803019,20.4046845\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.62118974,14.64857717,15.5584046,16.36498443,17.08110539,17.71803545,18.28563302\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,14.50813898,15.32042699,16.0480539,16.70182437,17.29105591,17.82366437,18.30634969\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.32482099,14.24167217,15.06962448,15.81800539,16.49505915,17.10811527,17.66371945\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,16.7878748,17.43816191,18.00077544,18.49644599,18.93914993,19.33841624,19.70091891\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,18.02674906,18.48198291,18.8934835,19.27100847,19.62013104,19.9441337,20.24511811\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.19524295,14.12021274,14.9557032,15.71111997,16.39475401,17.01396532,17.57532256\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.79693056,14.82549551,15.73251568,16.53357347,17.24248444,17.87128131,18.43036132\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,14.74180248,15.49395124,16.17177787,16.78476231,17.34086485,17.8467528,18.30803374\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Fe]1OO1, [O]O[Fe], topology \",,,13.10912596,14.15208016,15.078749,15.90323247,16.6380354,17.29410767,17.88099706\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,21.85502088,21.99742478,22.10864393,22.1971084,22.26859576,22.3271683,22.37574707\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,21.84389811,21.98863614,22.1015276,22.19122745,22.26365177,22.32295131,22.37210542\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,21.84526667,21.98963225,22.10227676,22.19180919,22.26411745,22.32333465,22.37242895\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,21.80224065,21.95388997,22.07212561,22.16603823,22.24183931,22.30388524,22.35530187\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.581860154,4.268001144,4.970274639,5.671614871,6.359128837,7.023888022,7.660335112\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.574857583,4.236925684,4.918330063,5.602436079,6.276313051,6.930719109,7.559653635\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.728373917,4.411048526,5.104965331,5.795007697,6.469861059,7.121734824,7.745819261\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.956830292,5.396449823,5.852044564,6.320586293,6.797314661,7.277096664,7.755237671\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,5.079753268,5.517355115,5.970252903,6.435540758,6.908595004,7.384416297,7.858430153\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,5.014119927,5.442121899,5.888338629,6.349437049,6.820282477,7.29537806,7.769710979\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.507246575,4.178347883,4.868962032,5.561948493,6.244051744,6.905868296,7.541356235\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.554651666,4.222004503,4.907984038,5.59586425,6.272773444,6.929593315,7.560463654\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.582815723,4.255808762,4.944675133,5.633411532,6.309791567,6.96521882,7.594227315\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.916052407,5.359682513,5.819142613,6.291313431,6.771393654,7.254245046,7.735190124\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,5.010511322,5.455556207,5.91555297,6.387418666,6.866444031,7.347612932,7.826379117\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.962519662,5.390389397,5.836232489,6.296957977,6.767590062,7.242718253,7.717361628\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.502827391,4.178406926,4.873046047,5.569497102,6.254470814,6.918581104,7.555834274\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.508034913,4.172171565,4.85663922,5.54435765,6.22207891,6.880346845,7.513024307\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.613950789,4.287519242,4.976330467,5.664520933,6.340000476,6.994291585,7.622024835\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.927090359,5.370796995,5.829767148,6.301074286,6.780063011,7.261697086,7.741365301\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,5.06424309,5.504419563,5.959423785,6.426385415,6.900741574,7.377560391,7.85233104\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.993955668,5.422385122,5.868644684,6.329584272,6.800203095,7.275093163,7.74929438\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.611530197,4.297240771,4.998324008,5.697967341,6.383504494,7.046183017,7.68056922\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.697608208,4.363740695,5.045715529,5.727811819,6.397939633,7.047552426,7.671187593\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.698678731,4.377757971,5.069284156,5.758021876,6.432465557,7.084622058,7.709498066\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.928720902,5.375383571,5.837472804,6.311891991,6.793857509,7.278254612,7.760437634\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.991554135,5.439950738,5.902984502,6.377622232,6.859179988,7.342658342,7.823527313\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.956808839,5.389029842,5.838550656,6.302337128,6.775473982,7.252612378,7.728832169\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.660573249,4.349563649,5.05293194,5.753960269,6.440100774,7.10272834,7.736533822\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.605577712,4.266666039,4.946994999,5.629994242,6.302764964,6.956080616,7.583948104\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.740619798,4.421564104,5.113940009,5.802683776,6.47647514,7.127492855,7.750889686\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.963869008,5.402934841,5.857955286,6.32595217,6.802186693,7.28153069,7.75928567\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,5.076861733,5.513503952,5.965460606,6.429892571,6.902212304,7.377434444,7.850983876\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,5.001622024,5.429992196,5.876616943,6.338184927,6.809559048,7.285228984,7.760165274\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.510126443,4.181794401,4.872854597,5.566174201,6.248509926,6.91047266,7.546035166\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.586088906,4.252610461,4.937322181,5.623669084,6.298912425,6.954029092,7.583222657\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.593329546,4.265969944,4.954518236,5.642963085,6.319067787,6.974226961,7.602968409\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.9253164,5.370309487,5.830869406,6.30388655,6.784579621,7.267837251,7.749012\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.990917805,5.438509444,5.900672322,6.374387822,6.854998004,7.337528663,7.817468423\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.954978516,5.38307456,5.829000898,6.28975072,6.760398278,7.235559158,7.710263089\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.516471101,4.192011977,4.88643505,5.582535142,6.267062292,6.930663783,7.567372564\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.475713065,4.133615619,4.813401443,5.497900529,6.173669178,6.831021207,7.46359591\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.567023077,4.236945635,4.923351895,5.610259504,6.285394483,6.940082369,7.568771253\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.947088479,5.386794583,5.842333785,6.310719407,6.7872386,7.266801026,7.744744921\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,5.068741773,5.506431064,5.959356388,6.424599897,6.897553592,7.373243207,7.8471184\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.999040907,5.425651266,5.870423004,6.330148657,6.799781604,7.273877,7.747444484\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.581220829,4.26030497,4.956981026,5.654085768,6.338546445,7.001232036,7.636391421\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.707103747,4.371318963,5.051807577,5.732773925,6.402035916,7.050957474,7.673998579\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,3.723421638,4.402892327,5.094643882,5.783445018,6.457791794,7.109695798,7.73417299\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.926937687,5.375399283,5.83898312,6.314635909,6.797608875,7.282817078,7.765641646\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.983017572,5.434095525,5.899399817,6.375941153,6.859076551,7.343845028,7.825752788\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,4.945811315,5.378446522,5.828390286,6.292617006,6.766210809,7.243817308,7.720509025\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.851304325,7.677685152,8.502153953,9.316430443,10.11346334,10.88736787,11.6334598\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.270243051,9.035946965,9.796301663,10.54697454,11.28266006,11.99809693,12.68871158\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.606267388,10.43323121,11.22683877,11.98362761,12.70159318,13.37986584,14.01844786\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.918329767,10.70573357,11.46137417,12.18345026,12.87071618,13.52245253,14.13845184\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.852754779,10.67447796,11.45506516,12.19454062,12.89346248,13.55264305,14.1730804\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.740601783,8.566215483,9.381409337,10.18044669,10.95781882,11.70871574,12.4293072\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.210905144,8.082457449,8.938682301,9.772547155,10.57876721,11.35339907,12.09364194\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.0479691,13.68616892,14.28811913,14.85526228,15.3881868,15.88742292,16.35378339\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.762475962,7.568506507,8.373045734,9.168596953,9.948650557,10.70768098,11.44120058\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.126722091,8.87827864,9.624481901,10.36137122,11.08416996,11.78810053,12.46893429\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.396551778,10.2028872,10.98120893,11.72748395,12.43901905,13.11425204,13.75254557\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.707914322,10.48880551,11.24236543,11.96560814,12.65634461,13.31313464,13.93523519\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.606363067,10.42400487,11.20487217,11.94771356,12.65208168,13.31804449,13.94606983\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.51718477,8.324619011,9.121572966,9.903401176,10.66545695,11.40349389,12.11396185\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.1022994,7.944953561,8.77658864,9.590530055,10.38137663,11.14479965,11.87748608\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.16305443,13.79387562,14.39009584,14.95244979,15.4810937,15.97631422,16.43880052\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.66569148,7.476256821,8.284059181,9.08173272,9.863087324,10.62293479,11.35706695\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.141300007,8.897554801,9.647282008,10.38678102,11.1114501,11.81664308,12.49823911\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.343622749,10.15757699,10.94289475,11.69547765,12.41261486,13.0927626,13.73532546\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.721139381,10.49697789,11.24570215,11.96461219,12.65162544,13.30530905,13.92487697\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.63897694,10.45270004,11.22993187,11.9694547,12.6708282,13.33411399,13.95976577\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.536084553,8.342255731,9.137948661,9.918554828,10.67944858,11.41639473,12.12584816\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.100728846,7.947385142,8.783208911,9.601253516,10.39592189,11.16276245,11.89839952\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.0440773,13.68338336,14.28630988,14.85425441,15.38780396,15.8875067,16.35420005\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.038501615,7.884587219,8.725045054,9.552060722,10.35882161,11.13963926,11.89005582\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.292394538,9.054656606,9.812119616,10.56030728,11.29384124,12.00741829,12.69643422\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.639224962,10.46345781,11.25407347,12.00774114,12.72258009,13.39782091,14.03353827\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.929550624,10.72360531,11.48481777,12.21131635,12.90194044,13.55611727,14.17379882\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.831981689,10.65902897,11.44400748,12.18708304,12.88894601,13.55052113,14.17289932\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.799317957,8.620402937,9.431581295,10.22712755,11.00147991,11.74975342,12.46804282\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.204392334,8.071350163,8.923143494,9.752869501,10.55534734,11.32670198,12.06416512\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.11932438,13.75421189,14.35388275,14.91928194,15.4506754,15.94840892,16.41320597\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.86138987,7.687951245,8.512537751,9.326952594,10.12417252,10.89830774,11.64465386\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.293349265,9.060399461,9.822346701,10.57473335,11.3121163,12.0291191,12.72108774\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.653981886,10.48301432,11.27766494,12.03467912,12.75223501,13.42961918,14.06696385\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.972154896,10.75503717,11.50603408,12.22353728,12.90643575,13.55409519,14.16635417\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.867330912,10.68750244,11.4655307,12.20189057,12.897482,13.55336019,14.17068347\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.778156196,8.591602275,9.395241201,10.18374561,10.95182458,11.69474485,12.40865561\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.239757636,8.113506058,8.971354455,9.806307714,10.61313,11.38793909,12.12800204\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.02253996,13.66399988,14.26829589,14.83717812,15.37144269,15.87175602,16.33901848\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.772382326,7.579945452,8.386804707,9.184985301,9.967647081,10.72905844,11.46462054\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.143788064,8.894304371,9.639878619,10.37641134,11.09901143,11.8028176,12.48354555\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.386742254,10.19574071,10.97641455,11.72474448,12.43805297,13.11479681,13.75436054\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.735320255,10.51245828,11.26283296,11.98336355,12.67178752,13.32660483,13.94702215\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.642404055,10.45632614,11.23377145,11.97350135,12.67506832,13.33852915,13.96433289\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.532473573,8.336044436,9.129553277,9.90837188,10.66784515,11.40370163,12.11235632\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.095206878,7.938436536,8.770888751,9.58576981,10.37759028,11.14196148,11.87553308\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.11953877,13.75450843,14.3543134,14.91980902,15.45123182,15.94892553,16.41362241\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.686985478,7.490891031,8.294075579,9.088568475,9.867745781,10.62611158,11.3592416\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.145783516,8.8999539,9.648354129,10.38707548,11.11134859,11.81639986,12.49801552\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.364627876,10.17933029,10.96535704,11.71855035,12.43616403,13.11663772,13.75937327\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.713093228,10.48312315,11.22720893,11.94251612,12.62681929,13.27854643,13.89678282\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.609692517,10.42339927,11.20049909,11.93990686,12.64125771,13.30464901,13.93054422\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.51782282,8.323867789,9.119585873,9.900316977,10.66140724,11.39860655,12.10836125\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.081928475,7.93021085,8.767817309,9.587692948,10.38415936,11.15270877,11.8899304\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.05299312,13.69117261,14.29303473,14.85999996,15.39266566,15.89158193,16.35758287\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.064385841,7.896366323,8.724254368,9.540261128,10.33757135,11.11044762,11.85433974\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,8.300450191,9.05858956,9.812317857,10.55730116,11.28819298,11.99966119,12.68704381\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.658900425,10.47624088,11.26116148,12.01024827,12.72147427,13.39391008,14.02748068\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.968624947,10.75713522,11.51341337,12.2355519,12.92234999,13.57318949,14.18797403\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,9.846713162,10.6690951,11.44974687,12.18887773,12.887212,13.54569057,14.16540214\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.833653708,8.640923429,9.438457695,10.22118447,10.9839571,11.72210797,12.43179928\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,7.217442244,8.082592383,8.932679598,9.760862869,10.56197485,11.33213271,12.06855277\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,13.14899317,13.78101505,14.37840147,14.94193101,15.47175198,15.96812887,16.43172975\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.164235304,7.014263777,7.891298623,8.777037658,9.655377417,10.51333761,11.34123368\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.101422404,6.951031973,7.828782058,8.715981614,9.596253997,10.45642969,11.28669374\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.189866558,7.040492103,7.917866312,8.803720329,9.681973356,10.53966791,11.36714489\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,6.101173136,6.950936856,7.828868581,8.716247932,9.596682405,10.4569956,11.28737102\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.19351182,15.97818774,16.68327627,17.31817639,17.89094229,18.4085194,18.87693996\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.85138219,15.70514675,16.46269808,17.13772935,17.7414667,18.28318113,18.77060808\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.40365438,15.25689351,16.01268342,16.68611897,17.28936628,17.8322373,18.32269572\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.10509552,15.91707956,16.64057068,17.28867659,17.87143497,18.39686263,18.87159124\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.68425159,15.50086527,16.23089209,16.88630345,17.47685901,18.0105914,18.49419347\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.34705045,15.22740047,16.00598087,16.69870925,17.31824679,17.87474475,18.37644287\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.54198678,15.41969231,16.19623225,16.88673649,17.50352157,18.05663729,18.5543483\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.18573655,16.03752186,16.79444343,17.46946126,18.07296268,18.61359262,19.09873255\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.34827676,16.12335962,16.81888135,17.44481474,18.00938843,18.51954282,18.98123679\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.01837948,15.84393332,16.57860228,17.23501228,17.82354121,18.35278676,18.82994946\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.61933503,15.44944434,16.18463341,16.83991003,17.42723675,17.95618099,18.43445996\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.30842468,16.0927342,16.7949876,17.42641939,17.99577577,18.5101821,18.97565248\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.26165444,16.01086734,16.68422198,17.29166967,17.84134453,18.339984,18.79325225\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.70659082,15.54452615,16.28769907,16.95058373,17.54473097,18.07943993,18.56229286\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,15.35672013,16.13841468,16.83314332,17.45366841,18.01034869,18.51162303,18.96443149\n\"linker [O-]C(=O)c1ccc2-c3c(C(c2c1)(C)C)cc(cc3)C(=O)[O-], nodes [Eu], topology dmd\",,,14.79953151,15.68465869,16.47237139,17.17536628,17.80407088,18.3673099,18.87269884\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,20.44514356,20.94812162,21.3520019,21.6804724,21.95072305,22.17542199,22.36404119\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,20.34423834,20.86160519,21.27718268,21.61524432,21.89342943,22.12474987,22.31894129\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,20.34986257,20.86528269,21.2795927,21.6168112,21.89442542,22.12535381,22.31927312\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,20.53049852,21.02107709,21.41486205,21.73506504,21.99849521,22.21752273,22.40138816\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.596449002,4.315090205,5.038689352,5.752851782,6.447152371,7.114635959,7.751196879\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.193534241,3.854987275,4.538671626,5.227642608,5.908639994,6.57208026,7.211622612\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.257775631,3.924371458,4.613854798,5.308507541,5.994491614,6.661853651,7.304061269\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.282161052,3.974090539,4.68173601,5.388376945,6.081418265,6.752096178,7.394891263\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.222387351,3.89359522,4.586039796,5.282386721,5.969203661,6.636880868,7.27914522\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.319089595,3.97366561,4.650477895,5.332715249,6.007171275,6.664271681,7.297663836\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,2.704403396,3.380779237,4.088192804,4.806133771,5.518551556,6.213860275,6.884389172\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.2797735,3.945714094,4.631600964,5.321124425,6.001413565,6.663128236,7.300092684\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.272392274,3.91362642,4.579706995,5.25437414,5.924261385,6.579326476,7.212670835\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.29242833,3.976807281,4.679556009,5.383570002,6.075719498,6.746731207,7.390668369\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.823861883,4.502097712,5.193286867,5.882095372,6.556567075,7.208226673,7.831696764\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,4.939094796,5.920366449,6.852775011,7.720337234,8.516368862,9.240151685,9.894496993\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.586874107,4.30565348,5.029492365,5.74396319,6.438615419,7.106474902,7.743422105\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.188128784,3.850138263,4.534478763,5.224136585,5.905804323,6.569869361,7.209975375\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.276603032,3.943007738,4.631977526,5.32589549,6.01100932,6.677432084,7.318679593\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.27428995,3.965114107,4.671996576,5.378168354,6.070979042,6.741611756,7.384500515\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.227351571,3.899588042,4.592715692,5.289458081,5.976445202,6.644123426,7.286265848\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.319649997,3.974013733,4.650648293,5.332741389,6.007085947,6.66410678,7.297449967\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,2.722301781,3.399300807,4.106993284,4.824925846,5.537108066,6.232009885,6.902008649\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.332932874,3.99627048,4.679240499,5.365802325,6.043227394,6.702242291,7.336695814\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.251511416,3.890890226,4.555929597,5.230261182,5.900367065,6.55605236,7.190285459\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.323235018,4.00452898,4.704231975,5.405436293,6.095090773,6.763933647,7.406006271\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.812729844,4.493265931,5.186698937,5.877584567,6.553907296,7.207169223,7.831994522\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,4.942022374,5.922025522,6.853493123,7.720363359,8.515889523,9.239305644,9.893387171\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.583662962,4.30222498,5.025916892,5.740306625,6.43493429,7.102815138,7.739819527\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.197900876,3.860206773,4.544628308,5.23420048,5.915660256,6.579432171,7.21918938\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.272571556,3.93919892,4.628414948,5.322589346,6.007960266,6.674634574,7.316124454\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.282490252,3.974001661,4.681263583,5.387569228,6.080327567,6.750772652,7.393379507\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.219051342,3.890966904,4.58397491,5.28075614,5.967899976,6.635818328,7.278256884\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.317719926,3.972314372,4.64914909,5.331417623,6.00591566,6.66306947,7.29652616\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,2.709325578,3.385903933,4.093399709,4.811328819,5.523664419,6.218840511,6.889202247\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.295740738,3.961917596,4.647893762,5.337404547,6.017598777,6.679146023,7.315877738\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.270429071,3.91307149,4.580566141,5.256577152,5.927683213,6.583809941,7.218045929\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.294397861,3.978022855,4.680317644,5.384121515,6.076236726,6.747328133,7.391409953\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.825356742,4.504629804,5.196799616,5.886481894,6.561693892,7.213952087,7.837883312\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,4.769034368,5.740838327,6.669261668,7.537037478,8.336307756,9.065388316,9.726343223\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.596117307,4.314334203,5.037498139,5.751252092,6.44519291,7.112375465,7.74869602\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.197632425,3.859191272,4.542893221,5.231812252,5.91270654,6.576008421,7.215389809\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.264343834,3.930634789,4.619719856,5.313923874,5.999442262,6.666345211,7.308115415\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.27486208,3.966267799,4.673627147,5.380170639,6.073256957,6.744082724,7.387096584\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.226363137,3.898087507,4.590861138,5.287383688,5.97425644,6.641898925,7.28406184\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.320017979,3.974514535,4.65126336,5.333451063,6.007869344,6.664942482,7.298316875\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,2.710421283,3.387070156,4.094632296,4.812614282,5.524985834,6.220180991,6.890546704\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.299932382,3.965662626,4.65116735,5.340226197,6.020009783,6.681195388,7.31761425\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.249404003,3.887958031,4.552286068,5.226050479,5.895736029,6.551135467,7.185198245\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.280761544,3.961805711,4.662128926,5.364557742,6.055825406,6.726506469,7.370523759\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,3.821813764,4.501139108,5.193440048,5.883307431,6.558736433,7.211226211,7.835391111\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,4.735525657,5.703279559,6.629500796,7.496447651,8.295860677,9.025742069,9.687922222\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.608574377,9.431035851,10.22512006,10.98933604,11.72185764,12.42099012,13.08547132\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.387069809,8.173185589,8.942330158,9.693815281,10.42594115,11.13642357,11.82285338\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.112486794,9.963561619,10.77669238,11.54954521,12.28112613,12.97138695,13.62094842\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.354922196,8.169773582,8.967484558,9.745746978,10.50198083,11.23348986,11.93775552\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.459348363,10.25588054,11.01601931,11.74015525,12.42864992,13.08185909,13.700221\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.600650861,10.40823926,11.17703509,11.90757183,12.60037241,13.25599396,13.87510746\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.900868656,10.6672356,11.40070087,12.10132794,12.76896335,13.4034542,14.00481106\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.601443435,10.3808633,11.12708225,11.83968725,12.51845824,13.16333816,13.77447244\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.464771541,8.274728814,9.067783004,9.841868552,10.59442185,11.32266636,12.02397811\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.068259774,9.970855728,10.82288921,11.62472482,12.37757441,13.08313113,13.74337059\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.384820639,8.189450483,8.974203687,9.738456013,10.48066549,11.198796,11.89074351\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.187908002,10.02213644,10.81505861,11.56748551,12.28024386,12.95416464,13.59014807\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.732747558,8.480508817,9.222787598,9.955834977,10.67531239,11.37688381,12.05665324\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.294627486,10.11254501,10.89375404,11.63824535,12.3459008,13.01669541,13.65083971\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.399817471,10.23139562,11.02511042,11.78058094,12.49748627,13.1757302,13.81555172\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.842955025,8.61653144,9.379378844,10.12829401,10.8595152,11.56927838,12.25423261\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.238631413,10.03426729,10.79475659,11.52062133,12.2121171,12.86940357,13.49270237\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,6.300128328,7.203995778,8.118446562,9.026122183,9.913601504,10.77101884,11.59156345\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.608512997,9.432935696,10.22870057,10.99433408,11.72803065,12.42811734,13.09335451\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.386509973,8.172365637,8.941410465,9.69290757,10.42511745,11.13572571,11.82230145\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.121677956,9.97295976,10.78624387,11.55918918,12.29080202,12.98103805,13.63052365\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.369197194,8.183794435,8.981314779,9.759406755,10.51546386,11.24677477,11.95081374\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.467235264,10.26182239,11.02050395,11.74354569,12.43121541,13.08379961,13.70168564\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.621411463,10.42707407,11.19416695,11.92320751,12.61469608,13.26916564,13.88726428\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.886238958,10.65410208,11.38901021,12.09097552,12.75982284,13.39539452,13.99770562\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.606979195,10.38528207,11.13065243,11.84261008,12.52088388,13.16537826,13.77620995\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.472749755,8.282153223,9.074786635,9.848517377,10.60074744,11.32868424,12.02969753\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.080813047,9.980511527,10.83007914,11.62983891,12.38095735,13.08508289,13.74414926\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.392692655,8.194529667,8.976767813,9.738817717,10.47914479,11.19570119,11.88635929\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.171087968,10.0039064,10.79557592,11.54700047,12.25903264,12.93249349,13.56825596\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.776153183,8.520729101,9.260148396,9.990668197,10.7079141,11.40750371,12.0854971\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.284356341,10.10429142,10.88734972,11.63351133,12.34265846,13.0147704,13.65006457\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.372781598,10.20244994,10.99465358,11.7490171,12.46519967,13.14306857,13.78281775\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.851536192,8.623922726,9.385833714,10.13403163,10.86471055,11.57406425,12.2587062\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.215566897,10.01701527,10.78235854,11.51225399,12.20707894,12.86709874,13.49262602\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,6.311094096,7.215882858,8.130782132,9.038590343,9.925993259,10.78319687,11.60343848\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.597722923,9.422449781,10.21829437,10.98389199,11.71750812,12.41751445,13.08269756\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.387481469,8.173233841,8.942084444,9.693342557,10.42530036,11.13566391,11.82201443\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.121899923,9.972628776,10.78541337,11.5579224,12.28916445,12.97909322,13.62833074\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.368090289,8.182846185,8.980375918,9.758385565,10.51431024,11.24546758,11.94935114\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.468635415,10.26362486,11.02251147,11.74562451,12.43327747,13.08578919,13.70356961\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.612505854,10.41889297,11.18657962,11.91611045,12.6080088,13.26282687,13.88122816\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.892326495,10.66027258,11.39504009,12.09673655,12.76524806,13.40045587,14.00239925\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.599558222,10.3794399,11.12601377,11.83889134,12.51787095,13.16290965,13.77416385\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.455181736,8.265401298,9.058732363,9.833087008,10.58589633,11.31438577,12.01593538\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.056094235,9.958964802,10.81129062,11.61342683,12.36658358,13.07245447,13.73301547\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.395579302,8.198768801,8.982164345,9.745189578,10.48631924,11.20351623,11.89466631\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.171346126,10.0066811,10.80035092,11.55331381,12.26649083,12.94077163,13.57709136\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.758901338,8.505365898,9.24641829,9.978337284,10.69677934,11.39739357,12.07626869\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.28705094,10.10721481,10.89040144,11.63659208,12.34568214,13.01767009,13.65279342\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.400951612,10.23206904,11.02526996,11.78023083,12.4966654,13.17449533,13.81396625\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.833861878,8.608680244,9.372696859,10.12268348,10.85486536,11.56547503,12.25116488\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.252525978,10.04946607,10.81073014,11.53697714,12.22856599,12.88573444,13.50876325\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,6.356229946,7.263030056,8.178551422,9.08592979,9.97216375,10.82771505,11.64601567\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.613373168,9.436110146,10.23038625,10.99472852,11.72732333,12.42648469,13.09095711\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.373630185,8.160233104,8.929959648,9.682073581,10.41484308,11.125963,11.81301089\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.112755156,9.963703356,10.77683847,11.54976857,12.2814622,12.97184765,13.62153149\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.367363307,8.181799007,8.979138784,9.757053452,10.51294955,11.24412285,11.94805082\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.467435327,10.2628832,11.0221543,11.74558219,12.43348909,13.0862032,13.704143\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.612800812,10.41939378,11.18724519,11.91690206,12.6088935,13.26377773,13.88222356\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.892942641,10.65997486,11.39408373,12.09531761,12.76351476,13.39851886,14.00034017\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.60658623,10.38585686,11.13194634,11.8444319,12.52308702,13.16785051,13.7788655\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.472459547,8.28229939,9.075279427,9.849300696,10.60177988,11.32993037,12.03112451\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.073043306,9.975014419,10.82652488,11.6279159,12.38038406,13.08561183,13.74556681\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.385981099,8.190361159,8.974767869,9.738644833,10.48049059,11.19829089,11.88995159\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.153560417,9.989831695,10.78440973,11.53825815,12.25229609,12.92740855,13.56452582\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.752969776,8.499248892,9.240073175,9.971786823,10.69007677,11.3906023,12.06945114\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.284979679,10.10365233,10.88558222,11.63078537,12.33914793,13.01063783,13.64545453\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.383672492,10.21475056,11.00804232,11.76322689,12.48000262,13.15826839,13.79824581\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,7.836370783,8.61084466,9.37448664,10.12411063,10.85596314,11.56628525,12.25173061\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.238481126,10.03632105,10.79838396,11.52535931,12.21762313,12.87542241,13.49904281\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,6.355254505,7.262420898,8.17802311,9.085308775,9.971355219,10.82667735,11.64474135\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.516089309,10.40431485,11.25475644,12.06565813,12.83540793,13.56288989,14.24765093\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.252894013,9.119289301,9.965454628,10.78653188,11.5779719,12.33595247,13.05762929\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.510730417,10.40232392,11.25564444,12.06895561,12.84068106,13.56974917,14.25575469\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.268478621,9.132369528,9.976310066,10.79544118,11.58520102,12.34174647,13.06220801\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.500375606,10.39268,11.24648631,12.06013045,12.83209232,13.56134165,14.24750179\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.227946734,9.09698476,9.945432138,10.76847718,11.56161714,12.32107181,13.04403311\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,9.541407476,10.42953638,11.27970189,12.09017914,12.8593842,13.58622689,14.27027769\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,8.235928313,9.103640207,9.951022204,10.77321739,11.56568071,12.32459541,13.04712338\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,13.50118095,14.46504623,15.32650075,16.09704867,16.78740058,17.4071165,17.96456958\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,16.11269013,17.01069099,17.79629331,18.48294191,19.08345898,19.60949263,20.07132737\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,16.93619189,17.91285332,18.71823703,19.386987,19.94637093,20.41772813,20.81776468\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,15.59430552,16.54156525,17.37232059,18.09972112,18.73666773,19.29508725,19.78563316\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,14.36410322,15.24837587,16.03702866,16.74195752,17.37364517,17.94113035,18.45215393\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,15.38849251,16.3663037,17.22202772,17.9697784,18.62336875,19.19549306,19.69741825\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,16.80389659,17.79318186,18.61044966,19.29001268,19.85905949,20.33897152,20.74654917\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,15.32081927,16.29729789,17.15370091,17.90351251,18.56001483,19.13550828,19.64098802\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,14.40778168,15.28492504,16.06760051,16.76754046,17.3950751,17.95910755,18.46726143\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,15.04797425,16.06064786,16.94759161,17.72297064,18.40087069,18.99433819,19.51500192\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,16.63210864,17.63983771,18.47345362,19.16732626,19.74883191,20.23957712,20.65658355\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,15.65272631,16.59537756,17.42191668,18.14544364,18.77883387,19.33399623,19.82156695\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,14.34995771,15.23252359,16.02009759,16.72441391,17.35583559,17.92331228,18.43451769\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,15.36498156,16.34822019,17.20813233,17.9591004,18.61516199,19.18918854,19.69258288\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,17.24117027,18.18008007,18.95327886,19.59465846,20.13074448,20.58221297,20.9652036\n\"linker [O]C1(OO1)c1ccc(cc1)n1cnc2c1cc1ccccc1c2, nodes [OH], [Zn], topology acs\",,,15.29780467,16.27604821,17.13428818,17.88586061,18.54398621,19.12094661,19.62773855\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,19.69319092,20.11056684,20.44521665,20.7169658,20.94020753,21.12554758,21.28091095\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,19.69325449,20.11062038,20.44526232,20.71700518,20.94024183,21.12557771,21.28093763\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,11.09143602,12.06971636,12.97879679,13.8178433,14.58821694,15.29279765,15.93543604\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,11.08596609,12.06501539,12.97474267,13.81433568,14.58517151,15.29014328,15.93311284\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,11.09136322,12.06964625,12.97872919,13.81777819,14.58815436,15.29273765,15.93537866\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,11.08592566,12.06497759,12.97470739,13.81430284,14.58514103,15.29011504,15.93308671\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.328692339,3.96794401,4.63247719,5.305311943,5.972832591,6.624989154,7.25497713\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.04384337,3.664905808,4.316928799,4.982525795,5.647423756,6.300830459,6.93521472\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.006511254,5.316796179,5.66918563,6.057817602,6.474632951,6.911169464,7.359639871\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,4.762094553,5.08936766,5.453838822,5.851264148,6.2747745,6.716716418,7.169810423\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.090087823,5.397009335,5.745535678,6.130006009,6.542518267,6.974714329,7.418866796\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.329623056,3.969098039,4.633777014,5.306694905,5.974250941,6.626408091,7.256372273\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.046427022,3.668112946,4.320607045,4.986541711,5.651665001,6.305205221,6.939649756\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.014832576,5.324617051,5.676644936,6.064989234,6.481552172,6.917850207,7.366085558\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,4.764827271,5.09226163,5.45697051,5.854650583,6.278396598,6.720535914,7.173781295\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.08695672,5.393950768,5.742561361,6.127117268,6.539713431,6.971991384,7.416224034\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.328610019,3.967854096,4.632382063,5.305213703,5.972732996,6.624889621,7.254878772\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.043694085,3.664742931,4.316755846,4.982346162,5.647240478,6.300646109,6.935031394\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.006574925,5.316862704,5.669254954,6.05788919,6.474706047,6.911243259,7.359713604\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,4.762250555,5.089522953,5.453994872,5.851421195,6.274932071,6.716873692,7.169966474\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.090116274,5.397027422,5.745545415,6.130008975,6.542515748,6.974707404,7.41885638\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.329725222,3.969210309,4.633896629,5.306819282,5.97437783,6.626535633,7.256498986\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,3.046404294,3.668089309,4.320582792,4.986517143,5.651640393,6.305180806,6.939625715\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.014665139,5.324443091,5.676464649,6.06480386,6.481363441,6.917659968,7.365895556\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,4.764809203,5.092224166,5.456915697,5.854581086,6.278315272,6.720445513,7.173684303\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,5.086965721,5.3939574,5.742565622,6.12711943,6.53971387,6.971990494,7.416222176\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,8.026364272,8.842608859,9.644538551,10.42781949,11.18779777,11.92023154,12.6217091\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.546787846,10.31268299,11.05109645,11.76023985,12.43842607,13.08433449,13.69714741\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.488781492,10.26381137,11.00935272,11.72406905,12.40664163,13.05603713,13.67165745\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.9463019,14.42868001,14.90135758,15.36091224,15.80377952,16.22707973,16.62889179\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,8.022530664,8.839357651,9.641814804,10.42555847,11.18593485,11.91870686,12.62046942\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.541504331,10.30799835,11.04692652,11.75651049,12.43507404,13.08130675,13.69439985\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.469332311,10.24602679,10.99304203,11.70906825,12.39280973,13.04325245,13.65981445\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.94538969,14.42865415,14.90202609,15.36211196,15.80537574,16.22896355,16.63097651\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,8.026343637,8.842584169,9.644509073,10.42778499,11.1877584,11.92018772,12.62166142\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.546784144,10.31267525,11.05108414,11.76022284,12.43840455,13.08430884,13.69711816\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.488740794,10.26377334,11.0093161,11.72403311,12.40660604,13.05600175,13.67162228\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.94645334,14.42881148,14.90147385,15.36101663,15.80387433,16.22716662,16.62897196\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,8.022493735,8.839325153,9.641786459,10.42553397,11.18591386,11.91868905,12.62045444\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.541495292,10.30799248,11.04692365,11.75651035,12.43507628,13.08131101,13.69440578\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,9.469338249,10.24603499,10.99305187,11.70907929,12.39282163,13.04326495,13.65982734\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.94543208,14.42867622,14.90203135,15.36210353,15.80535639,16.22893565,16.6309421\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,14.23930018,15.1356504,15.93423366,16.64816618,17.28791273,17.8621346,18.3782282\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.90496639,14.70592914,15.44929006,16.13586817,16.76711397,17.34528549,17.87331623\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.92818533,14.83487214,15.64534435,16.3720997,17.02513182,17.6127457,18.14207345\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,14.08952806,15.0039386,15.81814508,16.5455008,17.1967543,17.78084548,18.3054226\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.9133714,14.71298078,15.45534622,16.14117238,16.77183353,17.34953729,17.87718372\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.78896398,14.71165041,15.53587509,16.27443631,16.93762,17.5339911,18.07090368\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,14.23920233,15.13555088,15.93413473,16.6480693,17.28781886,17.8620443,18.3781418\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.90428754,14.70530469,15.44871501,16.13533812,16.76662495,17.34483386,17.87289866\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.92858176,14.83521793,15.64564689,16.37236552,17.02536652,17.61295396,18.14225918\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,14.08930725,15.00373484,15.8179578,16.54532894,17.1965966,17.78070067,18.30528946\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.91408763,14.71358614,15.45585786,16.14160532,16.7722007,17.3498496,17.8774503\n\"linker COP(=O)(c1ccc(cc1)P(=O)(OC)[O])[O], nodes [Cu], topology pts,bex\",,,13.78920789,14.71186176,15.53606053,16.27460076,16.93776714,17.53412376,18.07102403\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,18.17696116,18.74496765,19.21313936,19.60211226,19.92780462,20.20256102,20.43601138\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,18.18034359,18.74797325,19.21581363,19.60449797,19.92993998,20.2044793,20.43774117\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,3.493119075,4.164515271,4.853338063,5.543263786,6.221754552,6.879944978,7.512152078\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,3.493751042,4.165320237,4.8543091,5.544385392,6.223005325,6.881300497,7.513587281\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,3.493452433,4.164928621,4.853821239,5.543804301,6.222339306,6.880561394,7.512788756\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,3.494843393,4.166410573,4.855387805,5.545443396,6.224035181,6.882296661,7.514546018\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.471389035,8.320377951,9.15504912,9.969773036,10.75937255,11.51945628,12.24662858\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.476116998,8.325154731,9.159813453,9.974487237,10.76401146,11.52400166,12.2510665\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.115839232,7.94029485,8.753075856,9.547040735,10.3169991,11.05913685,11.77071251\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.119948656,7.945113566,8.758429623,9.552782856,10.3230066,11.06530754,11.77696252\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.467957986,8.317018136,9.151794347,9.966641778,10.75637407,11.51659414,12.24390276\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.476708566,8.325692529,9.160284991,9.974888815,10.76434468,11.52427111,12.25127828\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.121020454,7.944673881,8.756794896,9.550222836,10.31974863,11.06154036,11.77284033\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.117207096,7.94273803,8.756335399,9.550910684,10.32131426,11.06376432,11.77554559\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.468867498,8.317901598,9.152646918,9.967460224,10.75715635,11.5173392,12.24461031\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.475884966,8.324922001,9.159570055,9.974228425,10.76373599,11.52371046,12.25076177\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.120750547,7.944624634,8.756937454,9.55052566,10.32018035,11.06207179,11.77344565\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.117948361,7.943277101,8.756736299,9.551217891,10.32155853,11.06396679,11.77572063\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.471532444,8.320485571,9.155125147,9.969821184,10.75939628,11.51945885,12.24661306\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.475475889,8.324580887,9.159304213,9.974037798,10.76361606,11.52365432,12.25076145\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.117556379,7.941919448,8.754622927,9.548521949,10.31842316,11.06050998,11.77203902\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,7.118838874,7.944198475,8.757690282,9.552197524,10.32255284,11.06496383,11.77670929\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,9.388912857,10.19108612,10.96064081,11.69589455,12.3956275,13.05911482,13.68614007\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,9.387331703,10.18976251,10.9595922,11.6951152,12.39509841,13.05881033,13.68603206\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,9.387816681,10.19009623,10.95974076,11.6950696,12.39486538,13.05840571,13.68547631\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,9.387759822,10.19000769,10.95969259,11.69509961,12.39498958,13.05862676,13.68578911\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.63536568,14.54677678,15.36779805,16.10682184,16.7719793,17.37088297,17.91052192\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.42617774,16.96298251,17.44080599,17.87166657,18.26418465,18.62457654,18.95736814\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.47608142,14.40520804,15.24167395,15.9941195,16.67093109,17.27996202,17.82841803\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.40255256,16.94290524,17.42361999,17.85685809,18.25134748,18.61338604,18.94756236\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.6426833,14.55310904,15.37332658,16.11168615,16.77628824,17.37472285,17.91396219\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.45555904,16.98890824,17.46392097,17.89246491,18.2830483,18.64180353,18.97319344\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.45598308,14.38734838,15.22573842,15.97984238,16.65808811,17.26836383,17.81790446\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.38723394,16.92954636,17.41184448,17.84638235,18.24195416,18.60490587,18.93986146\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.63182336,14.54365961,15.36506901,16.10443712,16.76989493,17.36905801,17.90891985\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.46063548,16.99316048,17.46749914,17.89548842,18.28561261,18.64398553,18.97505558\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.48042794,14.40915006,15.24526088,15.99739402,16.67392975,17.28271613,17.83095445\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.38737791,16.92970139,17.41202448,17.84659038,18.24218813,18.6051616,18.94013414\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.62546127,14.53818157,15.36029754,16.10023921,16.76616951,17.36572707,17.90592223\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.42495915,16.96204099,17.44010024,17.87116057,18.26384707,18.62438019,18.95728947\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,13.48290225,14.411289,15.24712041,15.99902124,16.67536347,17.28398796,17.83209005\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cu], topology pts\",,,16.4017715,16.94207201,17.42274456,17.85594955,18.25041426,18.61243599,18.94660267\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,21.35821119,21.7023083,21.97499768,22.19435654,22.37319966,22.52077803,22.6438843\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,21.50139239,21.84562299,22.12038407,22.34272404,22.52488502,22.67580634,22.80211805\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,21.30235079,21.64766465,21.92082711,22.14023115,22.31887867,22.46613218,22.58885088\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,20.91384228,21.27973321,21.57170545,21.80791898,22.00140889,22.16168973,22.29581561\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,21.46864365,21.81681857,22.09272256,22.31464843,22.49556773,22.64484577,22.76935922\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,20.5699569,20.94729891,21.24815189,21.49136674,21.69046024,21.85528796,21.99314944\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,21.45102287,21.79698693,22.07072493,22.29063399,22.46972331,22.61736327,22.74042053\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,21.07272117,21.44118583,21.73510387,21.97280879,22.1674583,22.3286536,22.46351042\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.535073253,4.22054339,4.922782432,5.624807251,6.313619166,6.980104755,7.61851144\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.328654253,4.001591271,4.696144392,5.394664609,6.083368757,6.752370051,7.395221764\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.378101083,4.072952893,4.787235581,5.502518875,6.204768307,6.884204173,7.534695153\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.427754588,4.091316513,4.775055617,5.462247278,6.139821324,6.798389038,7.431816992\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.507854349,4.193276494,4.895424729,5.597383234,6.286181228,6.952710375,7.591211815\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.3068209,3.981066668,4.676719577,5.376120635,6.065497312,6.734984856,7.378163455\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.375143041,4.068438012,4.781466293,5.495793027,6.197363386,6.876367258,7.526638116\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.534788646,4.203576029,4.890098986,5.57807291,6.25489964,6.911616155,7.542439428\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.528980715,4.214467217,4.916860353,5.619145467,6.308293791,6.975165644,7.613986976\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.323971581,3.997658779,4.692953161,5.392168475,6.081501248,6.751056249,7.394386009\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.358039805,4.050343566,4.762833761,5.476960761,6.178569298,6.857769451,7.508335082\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.421574006,4.083829944,4.766516315,5.452925123,6.129987655,6.788306612,7.421734246\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.563073507,4.251311306,4.955005481,5.657453708,6.34591098,7.011476414,7.64856751\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.298714662,3.972826022,4.66881761,5.368894263,6.059169988,6.729692088,7.37397582\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.245844304,3.927452528,4.632331438,5.341723656,6.041089485,6.720103115,7.372120287\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,3.430982466,4.092296719,4.774035519,5.459512803,6.135676988,6.793144801,7.425779447\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.690212145,7.473230364,8.251298544,9.018822927,9.771088829,10.50396607,11.21389773\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,8.001572224,8.769738761,9.521765476,10.25683394,10.9729567,11.66757889,12.33810676\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.237802322,10.04448671,10.82229288,11.56786922,12.27891196,12.95404599,13.59269308\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.571840855,8.419248079,9.249282354,10.05716891,10.83865942,11.59019863,12.30905216\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.950775065,7.85627598,8.744232738,9.607642951,10.44098755,11.24009931,12.00206437\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.582485551,8.409647766,9.219854419,10.00973772,10.77587993,11.51508164,12.22462605\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.221341162,10.02993746,10.80916548,11.5560939,12.26860115,12.9453671,13.58580605\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.898162369,7.81036413,8.70396058,9.572132795,10.40948056,11.21192089,11.97660944\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.608319152,8.475036672,9.320617602,10.14055111,10.93094689,11.68866181,12.41138777\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.087922288,9.905297866,10.69225128,11.44560511,12.16318764,12.84373632,13.48677927\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.650184204,8.436719407,9.208469459,9.963088875,10.69756224,11.40871626,12.09365027\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.237043674,10.03703215,10.80869786,11.54889536,12.25521342,12.92607634,13.56071432\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.272017431,8.135044908,8.983516261,9.810853157,10.61174686,11.38201988,12.11858207\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.536796424,7.305454341,8.073584944,8.834418269,9.582256315,10.3122326,11.02027334\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.031429311,6.816882716,7.598378032,8.369088474,9.123770375,9.858157331,10.56875433\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.723856769,7.500476576,8.275760718,9.043397937,9.797751547,10.53384779,11.2474684\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.142030506,6.923445334,7.700923267,8.468360981,9.220708091,9.953625081,10.66343623\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.853177551,8.635237576,9.400210834,10.14697973,10.87336564,11.57673219,12.25449623\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.136452072,9.952971819,10.7396296,11.49303822,12.21085813,12.89170397,13.53502131\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.517102368,8.381368005,9.22634752,10.04692952,10.83875709,11.59833567,12.32310235\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.932394815,7.840479574,8.730401167,9.595252258,10.42960072,11.22935501,11.99166627\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.512869459,8.338794894,9.148805128,9.939273722,10.70651834,11.4471098,12.15815218\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.091322597,9.904234223,10.68733874,11.43763804,12.15298019,12.83204523,13.47427141\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.905959551,7.817322935,8.710413686,9.578368988,10.41570896,11.21826983,11.98314006\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.544574157,8.40611975,9.248637034,10.06719187,10.85749564,11.61605822,12.34028497\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.197268927,10.01408855,10.80091001,11.55441592,12.27231809,12.95326505,13.59672172\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.896684491,8.684270311,9.457444542,10.21370796,10.94994076,11.66289762,12.34962742\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.514419165,10.31681351,11.09081972,11.8331634,12.54134457,13.21373888,13.84956051\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.376874794,8.241444042,9.090482891,9.917901256,10.71867241,11.48877504,12.22519957\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.723861448,7.497950638,8.267907125,9.028156791,9.77397019,10.50121517,11.20633995\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.634537459,7.43244967,8.225499056,9.0069824,9.77161967,10.51506858,11.23377455\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.643074763,7.419052938,8.192065751,8.956191169,9.706207871,10.43752636,11.14624899\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.609857634,7.389016966,8.164169125,8.929432111,9.679918072,10.41138662,11.12020537\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.971232988,8.738985243,9.490598786,10.22529164,10.94109602,11.63546585,12.30580904\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.244706819,10.05325116,10.8329834,11.58043813,12.29322701,12.96992165,13.60991741\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.641030995,8.488604605,9.319375682,10.12835892,10.91113497,11.66402054,12.3841925\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.961604081,7.867095659,8.755314753,9.619158389,10.45303425,11.25272444,12.01528159\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.572181814,8.400330983,9.212292699,10.00436564,10.7728719,11.51442552,12.22618695\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.198889433,10.01060007,10.79313608,11.54333862,12.25892421,12.93847073,13.58133934\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.883812236,7.794540538,8.687377962,9.555340309,10.39286685,11.19573873,11.96100601\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.534959898,8.394722084,9.23474338,10.0503811,10.83758801,11.5930583,12.31432743\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.067879966,9.879448976,10.66156307,11.41090396,12.12518116,12.80303139,13.44389608\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.613749161,8.399674183,9.171565683,9.926910562,10.66253758,11.37513937,12.06170587\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.22554597,10.0243594,10.7956602,11.53607231,12.24297598,12.91462829,13.55013639\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.274479718,8.13622901,8.983743708,9.810446938,10.61098922,11.38113787,12.11774761\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.603843229,7.375054354,8.145005783,8.907126177,9.655881126,10.38653333,11.09510626\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.206161079,7.003808885,7.795610277,8.575033423,9.337047119,10.07756165,10.79324026\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.756909152,7.531916341,8.30642891,9.07385409,9.828348845,10.56479226,11.27886423\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.634156924,7.413999453,8.190282055,8.956838193,9.708559463,10.441056,11.15060966\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.9390152,8.7201313,9.48462337,10.23126733,10.95778322,11.66144895,12.33961407\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.13536271,9.953066693,10.74136272,11.49666229,12.21646791,12.89928182,13.54447635\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.460651059,8.323737296,9.168536091,9.989639957,10.78247208,11.54337725,12.26967609\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.892336018,7.801310484,8.692629288,9.559151447,10.39526092,11.19673654,11.96064715\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.548100491,8.377444352,9.191407968,9.986009059,10.75728884,11.5016275,12.21601444\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.174329223,9.990223296,10.77638652,11.52966657,12.24780353,12.92941159,13.57389684\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.835524058,7.747461556,8.64135325,9.510203626,10.34843098,11.15180138,11.91736105\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.474937424,8.338722339,9.182292131,10.00098642,10.7907633,11.5483409,12.27129181\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,8.990512028,9.803071277,10.58565879,11.33524554,12.04970249,12.72774636,13.36885105\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.603338312,8.392204156,9.166570793,9.923875197,10.6609445,11.37450246,12.06158957\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,9.171728842,9.966529438,10.73365578,11.4699538,12.1729639,12.84104687,13.47336675\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.160351881,8.019450175,8.863911944,9.687400962,10.48478574,11.25199866,11.98600159\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.455683853,7.221285138,7.985231676,8.74129057,9.484231738,10.20954726,10.9134068\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.497757629,7.293515288,8.086669024,8.869807742,9.637029461,10.38349356,11.10527751\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.77677503,7.553543818,8.327927574,9.093736342,9.845539306,10.57859766,11.28891724\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.041660199,7.818009267,8.583411249,9.332831853,10.06219505,10.7680978,11.44776198\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.788912758,8.585852328,9.373172021,10.14453994,10.89476034,11.61961505,12.31582774\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.671335547,7.459557433,8.238743872,9.002643699,9.746178891,10.46521385,11.15650056\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.50899745,8.291476619,9.062757863,9.817479746,10.55135167,11.26086016,11.94320119\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.552447929,8.329713188,9.096003011,9.846353059,10.57669336,11.28359997,11.96426669\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.580171605,8.365835325,9.138759181,9.894074973,10.62784335,11.33680475,12.01833822\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,6.704481247,7.485038985,8.255066967,9.009052333,9.742589378,10.45207905,11.13465258\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,7.382192576,8.171664102,8.951999172,9.716916467,10.46132432,11.18108957,11.87297736\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.53455129,15.35938698,16.09006489,16.74123189,17.32461586,17.84964079,18.32394745\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.75817949,15.53376109,16.23446058,16.86811728,17.44193514,17.96235897,18.43508313\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.77436072,16.41552773,16.99891311,17.53192762,18.02019323,18.46817767,18.8795936\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.64284638,16.26434416,16.83197156,17.35211115,17.82977363,18.26902641,18.6732899\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,13.79224956,14.38157624,14.91979838,15.41373345,15.86854859,16.28826731,16.67613017\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.04822904,15.61280993,16.13279401,16.61297873,17.05707082,17.46806117,17.8484794\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.68024035,15.36982134,15.9958741,16.56462966,17.08193162,17.55304698,17.98264901\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,13.18722239,13.79460925,14.34903237,14.8558881,15.32009614,15.74597275,16.13725748\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.75626506,15.38242592,15.94926553,16.46486763,16.93522399,17.36505052,17.75825846\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.09123888,15.73993309,16.31992659,16.84219067,17.3152916,17.74596044,18.13954091\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.92573323,15.77186093,16.52276419,17.19227178,17.79139155,18.32910279,18.81288894\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.20576056,15.89450812,16.50745195,17.05719773,17.5534275,18.00367359,18.41388369\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,12.90753371,13.63674096,14.2891324,14.87548201,15.40466007,15.88394557,16.31934388\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.1548782,14.87452521,15.5285146,16.12266996,16.66275776,17.15415177,17.60172279\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.70711607,16.30948915,16.86134554,17.36857581,17.83572263,18.26643635,18.66377904\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.85357608,15.41175865,15.92571295,16.400204,16.8390449,17.24534399,17.62171121\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.10913457,14.709352,15.25876041,15.76325016,16.22740352,16.65492684,17.04894215\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,13.54067124,14.11567531,14.64355243,15.12964213,15.57807728,15.99218451,16.3747585\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.97984507,15.73774143,16.42062832,17.03733266,17.59549973,18.10170783,18.56162403\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.63016515,16.27000867,16.84971787,17.37687746,17.85777819,18.29762764,18.70076829\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.48235428,16.22229029,16.88288365,17.47667664,18.01303073,18.49920197,18.94102131\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.63594716,16.30321686,16.89927563,17.43556437,17.92102258,18.36267395,18.76609103\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.74333484,15.59795477,16.35592612,17.03139465,17.63558895,18.17764884,18.66517961\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.37082914,16.04049609,16.63677654,17.17202923,17.65573434,18.09524509,18.49633972\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.88517802,15.62426675,16.28508002,16.87872928,17.41429619,17.89920648,18.3395765\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.58249704,15.34144932,16.02860535,16.65107726,17.21555592,17.72811084,18.1941539\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.62452519,16.26102077,16.84118602,17.37223979,17.85970136,18.30794713,18.72058436\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.50326145,15.07254967,15.59551424,16.07758064,16.52294279,16.93493726,17.31631998\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.4494769,15.04557277,15.58876269,16.08633793,16.54380409,16.96543145,17.3546434\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.88109441,16.48215982,17.03189215,17.53665317,18.00125117,18.42948484,18.82449576\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.96808425,15.69994438,16.36108543,16.95957107,17.50244697,17.99580724,18.44492075\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,12.56100855,13.20315066,13.78768268,14.3208877,14.80833792,15.25484694,15.66454388\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.85607279,15.49005365,16.06358741,16.58505948,17.06065521,17.49521583,17.89273591\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.46452835,16.12762763,16.71982541,17.25255415,17.73473315,18.17336201,18.57398897\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.22383062,16.03050849,16.74798599,17.38912422,17.96407525,18.48109679,18.94707746\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.57684032,16.25952331,16.86772744,17.41369606,17.90685546,18.35455652,18.76261749\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.22097943,15.94508415,16.59143134,17.17163666,17.69496216,18.16884542,18.59933357\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.80986631,15.51849217,16.16453578,16.75289207,17.28871193,17.77695102,18.22218946\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.33606947,15.95560723,16.52167242,17.04069856,17.51761421,17.95637023,18.36027916\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.65640323,15.21675973,15.73347792,16.21097317,16.65277192,17.06177757,17.44047276\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,14.02843705,14.60082281,15.12551533,15.60841299,16.05405977,16.46604736,16.84730994\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,13.78832285,14.35235526,14.87180051,15.35144578,15.79493293,16.2051898,16.58470483\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.15299385,15.88201724,16.53921785,17.13290415,17.67031554,18.15770725,18.60048745\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.71486066,16.35424151,16.93451694,17.46273169,17.94483283,18.38581872,18.78991423\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,13.28262681,13.87512976,14.41427024,14.90710219,15.35878635,15.77335218,16.15413658\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.05238676,15.71925015,16.31479603,16.85045462,17.33516358,17.77595339,18.1784097\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.06905429,15.88464809,16.6102256,17.25860501,17.83994779,18.36255453,18.83337673\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(c(c1)N(=O)=O)c1c(cc(cc1N(=O)=O)C(=O)[O-])C(=O)[O-], nodes [Mn], topology pcu,\",,,15.54551465,16.24234279,16.86027705,17.41302399,17.9110299,18.36235308,18.77329539\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,17.12698594,18.09865012,18.9118551,19.59527066,20.17257094,20.66298437,21.08201077\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,17.20133242,18.22600549,19.06912724,19.76752207,20.35028484,20.84020317,21.25509925\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,17.01271578,18.02947598,18.87373564,19.5784828,20.17038512,20.67072972,21.096432\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,16.28672321,17.38912666,18.30762283,19.0762168,19.72290867,20.27031457,20.73655013\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,17.12633393,18.09807974,18.91135452,19.59482941,20.1721801,20.66263645,21.08169954\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,17.20122429,18.22592145,19.06906158,19.76747037,20.35024378,20.84017026,21.25507264\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,17.01311606,18.02985649,18.87409172,19.578813,20.17068979,20.67101014,21.09668989\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,16.28619001,17.38863722,18.30717666,19.07581129,19.72254038,20.26997985,20.73624544\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.313326776,3.987352837,4.684418857,5.386287094,6.0787036,6.751465253,7.397945682\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.522163995,4.219645044,4.934203346,5.647748462,6.346644275,7.021502773,7.666539535\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.462695154,4.160815184,4.875297,5.588453277,6.286995354,6.961783955,7.607188891\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.293076107,3.974386245,4.678175332,5.385966328,6.083409895,6.760306316,7.410091932\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.46437007,4.157812165,4.869793377,5.582062455,6.280758938,6.956262444,7.602576905\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.265088639,3.948344775,4.654669104,5.365148035,6.065206075,6.744549439,7.396596066\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.31335619,3.987390813,4.684464558,5.38633927,6.078760865,6.751526259,7.398009214\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.521732737,4.219167058,4.933693742,5.647219959,6.346107162,7.02096511,7.66600746\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.462725837,4.160847011,4.875331113,5.588490092,6.287034818,6.961825748,7.607232563\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.293049721,3.974358684,4.678147367,5.385938519,6.083382629,6.760279842,7.410066396\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.464259366,4.157693017,4.869668402,5.581934091,6.28062929,6.956133235,7.602449489\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,3.265134936,3.948400529,4.654731926,5.365215792,6.06527695,6.744621952,7.396669042\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.593631121,7.362406563,8.129425244,8.88840391,9.634041302,10.36175374,11.06764861\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.659085611,7.420642433,8.180852872,8.933035202,9.671800593,10.39264218,11.09180774\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.727560227,8.509878822,9.279501454,10.03348263,10.76833232,11.48052156,12.16689248\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.072538608,9.875555666,10.65370762,11.40284057,12.11961102,12.80168784,13.44773927\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.710141466,8.503576422,9.284859734,10.05019141,10.79552531,11.51701506,12.21136257\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.249911388,10.03907849,10.80473426,11.543087,12.25072119,12.92506374,13.56450486\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.421333053,8.254922048,9.069478886,9.86207132,10.62972014,11.36957318,12.07916476\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,8.944987445,9.756838149,10.54132477,11.29493646,12.01491397,12.69940494,13.34743937\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.591543006,7.366242702,8.138665083,8.902212022,9.651376941,10.38151988,11.08881219\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.697219506,7.471539815,8.243821485,9.006986163,9.75534812,10.48423472,11.18985157\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.740990332,8.514619431,9.276184688,10.02287504,10.75128376,11.45791569,12.13960375\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.003658171,9.822711517,10.61490943,11.37622731,12.10345932,12.79442125,13.44793542\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.700400564,8.496884426,9.279339578,10.04461952,10.7891586,11.50945284,12.20243961\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.179193648,9.960268881,10.71887898,11.45135575,12.15431902,12.82516319,13.46219894\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.417863448,8.229417917,9.022118631,9.794047595,10.54296866,11.26647414,11.96228433\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.037563729,9.82292858,10.58352674,11.31606893,12.01780866,12.68677124,13.32178389\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.593666447,7.36244044,8.129458108,8.888435948,9.634072579,10.36178426,11.06767837\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.65921915,7.420744529,8.180931232,8.933095354,9.67184658,10.39267702,11.09183371\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.727565418,8.509883504,9.279506446,10.03348828,10.76833871,11.48052863,12.16690011\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.072613196,9.87562723,10.65377551,11.40290422,12.11967007,12.80174213,13.44778882\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.710209155,8.503635657,9.284913802,10.05024197,10.79557311,11.51706039,12.21140551\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.250417598,10.03952332,10.80512759,11.54343645,12.25103286,12.92534263,13.56475515\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.421390161,8.254969032,9.069517024,9.862101638,10.62974353,11.36959046,12.07917668\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,8.945126815,9.756965215,10.54144031,11.29504122,12.0150087,12.6994904,13.34751632\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.591413749,7.36616122,8.138622328,8.902200965,9.651391866,10.381556,11.08886545\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,6.69742899,7.471693721,8.243934728,9.007069563,9.755409642,10.48428027,11.18988553\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.740888619,8.514543627,9.27612982,10.02283697,10.75125906,11.45790158,12.13959798\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.00369688,9.822742901,10.61493325,11.37624375,12.10346889,12.79442463,13.44793338\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.700375862,8.496861302,9.279319348,10.04460256,10.7891448,11.50944183,12.20243099\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.179128529,9.960210867,10.71882665,11.45130808,12.15427527,12.82512279,13.46216146\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,7.417831664,8.229395043,9.022102917,9.794037687,10.54296348,11.26647281,11.96228614\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,9.037467672,9.822850193,10.58346179,11.31601445,12.01776254,12.6867319,13.32175014\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,11.57002121,12.356118,13.09000752,13.77749831,14.42241212,15.02738746,15.59443485\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,11.57788123,12.32839495,13.03283859,13.69643734,14.32239704,14.91272638,15.468819\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,11.57045015,12.35651971,13.09038438,13.77785221,14.42274463,15.02769998,15.59472866\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,11.57779486,12.32831527,13.03276497,13.69636933,14.32233429,14.91266852,15.46876569\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.47274849,16.15867242,16.77350443,17.32803435,17.83060634,18.28779647,18.70490103\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.05898044,15.76838401,16.40998069,16.992163,17.52185175,18.00481889,18.44594718\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.02412504,15.76719054,16.43466264,17.03655767,17.58105545,18.07492559,18.52385114\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.79859154,16.40654274,16.96051309,17.46668581,17.93035303,18.35600148,18.74743716\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,14.78605638,15.58109532,16.29521212,16.9383004,17.51860301,18.04312583,18.51791995\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.31377517,16.03683647,16.69083593,17.28342178,17.82109183,18.30946812,18.75348881\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.81727558,16.41884124,16.96454682,17.46159536,17.9160455,18.33291372,18.7163386\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.48224921,16.15555793,16.75492221,17.29273752,17.77857478,18.21988717,18.62254262\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.47369743,16.1594838,16.77420666,17.32864843,17.83114811,18.28827811,18.7053321\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.05894156,15.76836669,16.40997898,16.99217247,17.52186911,18.00484169,18.4459736\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.02979282,15.77211309,16.43897181,17.04035726,17.58442786,18.07793684,18.52655465\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.80144563,16.40903729,16.96271034,17.46863452,17.93209199,18.35756193,18.74884454\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,14.78607231,15.58112624,16.29525161,16.93834448,17.51864923,18.04317264,18.51796641\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.32075495,16.04293084,16.69619845,17.28817291,17.82532737,18.31326516,18.75691009\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.81846989,16.41986092,16.96543179,17.46237408,17.91673871,18.33353683,18.71690327\n\"linker [O-]C(=O)c1cc([N][N]c2cc(cc(c2)C(=O)[O-])C(=O)[O-])cc(c1)C(=O)[O-], nodes [Li], topology \",,,15.4758865,16.15006248,16.75013166,17.28852684,17.77484638,18.21656394,18.61956289\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,21.63755704,21.89589871,22.10085837,22.26594356,22.40070571,22.51203745,22.60500348\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,21.63687983,21.89534521,22.10039652,22.26555172,22.40036868,22.51174426,22.60474593\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,21.63645823,21.89498569,22.10008763,22.26528425,22.40013528,22.51153908,22.60456434\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,21.63675022,21.89521595,22.10027436,22.26543909,22.40026604,22.51165115,22.60466159\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,17.68280426,18.49085406,19.16830359,19.73934522,20.22342435,20.63614352,20.99002877\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,17.68253098,18.49068481,19.16821365,19.73931419,20.22343616,20.63618586,20.9900924\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.336580746,3.988059172,4.664897308,5.349398372,6.027465505,6.688783686,7.32645364\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.428737463,4.090966526,4.776538403,5.467649338,6.1503007,6.814402103,7.45333881\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.417038923,4.077975453,4.762467556,5.452712901,6.134692361,6.798278228,7.436809672\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.33692293,3.988428793,4.665286279,5.349799433,6.027872443,6.689191378,7.326858003\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.429019797,4.091287987,4.776887267,5.468015639,6.15067632,6.814780642,7.453715362\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.417072144,4.078007138,4.762495042,5.452735008,6.134708821,6.798289285,7.436815833\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.336833226,3.988350917,4.665219935,5.349743796,6.027826384,6.689153654,7.326827377\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.428882824,4.091120279,4.776698884,5.467814362,6.150468039,6.81456974,7.453505046\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.416505421,4.077394175,4.761854902,5.45208279,6.134056059,6.797644513,7.436185158\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.336882838,3.988405013,4.665273677,5.349794227,6.027871926,6.689193656,7.326861775\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.42906692,4.091358924,4.776977691,5.468121349,6.150793487,6.814905927,7.45384595\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,3.416406222,4.077317739,4.761792655,5.452029231,6.134007779,6.797599475,7.436142199\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.795983915,7.626924795,8.445864041,9.247626601,10.02795257,10.78323829,11.5105146\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.424509897,10.19632829,10.94823066,11.67549399,12.37417958,13.04139766,13.67531623\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.476869265,10.2550921,11.01202159,11.74305193,12.44438362,13.1132739,13.74803672\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.912885855,7.672618589,8.431970806,9.185587708,9.928227439,10.6549396,11.36131491\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.767919318,7.588219715,8.398590029,9.194090553,9.970344575,10.72345305,11.45008797\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.985089666,8.779543291,9.55719955,10.31622265,11.05396936,11.7675311,12.45419614\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,8.000375926,8.787868162,9.558821342,10.31169002,11.04398982,11.75287511,12.43563212\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.425789763,10.20323183,10.96017725,11.69168662,12.39377708,13.06360556,13.69942912\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.971991339,8.752299151,9.518796079,10.26911702,11.00019453,11.7087742,12.39185665\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.796716518,7.627562943,8.446416185,9.248101389,10.02835869,10.78358422,11.51080831\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.424217901,10.19610944,10.94807981,11.6754053,12.37414655,13.04141342,13.67537392\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.476252945,10.25451192,11.01147368,11.74253263,12.44388976,13.11280284,13.74758636\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.91291025,7.672675601,8.432051222,9.18568533,9.92833781,10.65505934,11.36144134\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.767649306,7.588094099,8.398575754,9.194161193,9.970478997,10.72363443,11.450303\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.984342109,8.778833337,9.556514216,10.31555361,11.0533119,11.76688305,12.45355702\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,8.000559923,8.788102512,9.55909291,10.31198804,11.04430553,11.7532015,12.4359636\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.426072697,10.20349189,10.96040442,11.69187522,12.39392485,13.06371277,13.69949777\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.972590391,8.752812386,9.519233022,10.26948642,11.00050441,11.70903194,12.39206897\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.796649691,7.62746102,8.446310747,9.248012664,10.02829854,10.78355852,11.51081882\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.42461523,10.19652128,10.94849488,11.67581576,12.37454709,13.04180061,13.67574566\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.477336418,10.25550179,11.01238055,11.74336566,12.4446569,13.11351109,13.74824183\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.913260019,7.672881153,8.432141691,9.1856829,9.928260165,10.65492102,11.36125453\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.765774948,7.586627683,8.397446565,9.193311816,9.969861823,10.72320952,11.45003671\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.985278515,8.779726527,9.557374173,10.31638695,11.05412253,11.76767295,12.45432692\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,8.000364117,8.787924343,9.558924198,10.31182371,11.04414274,11.75303893,12.4358009\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.426576268,10.20395336,10.96083608,11.69228547,12.39431919,13.06409464,13.69986921\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.971503988,8.751791432,9.518276885,10.26859334,10.99967186,11.70825683,12.39134789\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.796004804,7.626947101,8.445882374,9.247638866,10.02795853,10.78323867,11.51051048\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.423748865,10.19566804,10.94765847,11.67499867,12.37375119,13.04102734,13.67499616\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.475994927,10.25428812,11.01128133,11.74236876,12.44375135,13.11268699,13.7474903\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.912873721,7.672578094,8.431905033,9.185500517,9.928122903,10.65482164,11.36118706\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,6.768371915,7.588650725,8.399005911,9.194494688,9.970738429,10.72383697,11.45046175\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.984173025,8.778682201,9.556381329,10.31543833,11.053213,11.76679902,12.45348623\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,8.000646877,8.788172378,9.559148775,10.3120318,11.04433841,11.75322444,12.43597742\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,9.425245151,10.20272425,10.95969001,11.69120896,12.39330264,13.06313111,13.69895354\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,7.97306434,8.753221821,9.519584912,10.26978832,11.00076369,11.70925533,12.39226237\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,23.36302786,23.4417087,23.50214546,23.54954611,23.58739206,23.6180797,23.64330101\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,23.36297523,23.44166613,23.50211024,23.54951644,23.58736669,23.61805774,23.64328179\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,23.36207221,23.44091196,23.50147147,23.54896881,23.58689221,23.61764281,23.64291595\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,23.36333378,23.44196422,23.50236189,23.54973166,23.58755282,23.61822028,23.64342495\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.37619463,15.22972704,15.99150917,16.67457272,17.28933649,17.84429534,18.34650888\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.78915489,14.6758888,15.47554967,16.19728477,16.84944169,17.43949734,17.97409116\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.7281697,15.53706759,16.25663638,16.90027388,17.47881745,18.00104228,18.47410488\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.2153345,15.07629191,15.8438708,16.531672,17.15055028,17.70930645,18.21519686\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.70310397,14.63944649,15.4690669,16.20767743,16.86819329,17.46121472,17.99548474\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,12.98898024,13.95650171,14.8265273,15.60986205,16.31617359,16.9540087,17.53088848\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,15.71038754,16.75345484,17.65015534,18.42104593,19.08483751,19.65792578,20.15435184\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.37634018,15.22984795,15.99158124,16.67458785,17.28929532,17.84420289,18.34637206\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.77200463,14.66047606,15.46164822,16.18470376,16.8380188,17.42909377,17.96458768\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.7224639,15.53235759,16.25271483,16.89698438,17.47603988,17.99868295,18.4720898\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.22031166,15.08089362,15.84811632,16.5355886,17.15416731,17.71265238,18.21829803\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.70788943,14.64381149,15.47303684,16.2112837,16.87146911,17.46419274,17.99819573\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,12.98883343,13.95605813,14.82588519,15.60909015,16.31532008,16.95310754,17.52996373\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,15.68381121,16.72992203,17.62926691,18.40244309,19.06820751,19.64300037,20.14090275\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.38694841,15.23927899,16.00002037,16.68218416,17.29616934,17.85045284,18.35207872\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.74045905,14.63252895,15.43669574,16.16227546,16.8177424,17.4106702,17.94777334\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.74318382,15.5502879,16.26835485,16.91072563,17.48819276,18.00949613,18.48176437\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.22045261,15.08086936,15.84798311,16.53538351,17.15391504,17.71236965,18.21799636\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.70368221,14.64024758,15.47000676,16.20869987,16.86926049,17.46230098,17.9965724\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,12.99392043,13.96081884,14.83033909,15.61325926,16.31922629,16.95677139,17.53340406\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,15.69454077,16.73943786,17.63772367,18.4099815,19.07495128,19.64905624,20.14636198\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.37606964,15.22958919,15.99137935,16.67446196,17.28924971,17.84423373,18.3464715\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.79251522,14.67893519,15.47832053,16.19981272,16.85175469,17.44161948,17.97604325\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.72159205,15.53146447,16.25182323,16.89610727,17.47518472,17.99785406,18.47128961\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,14.21605319,15.07698779,15.84453694,16.53230512,17.15114931,17.70987165,18.21572925\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,13.70471731,14.64081056,15.47022535,16.2086656,16.86903989,17.46194315,17.99611416\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,12.98560287,13.95348221,14.82382238,15.60743232,16.31398423,16.95202941,17.52909311\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In]O[Co]O[In], topology sql\",,,15.72349005,16.76510337,17.66055488,18.43036757,19.09322514,19.66550101,20.16121788\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,19.48795829,19.95390669,20.32337585,20.62073445,20.8632841,21.0635234,21.23063254\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,19.39080509,19.87127806,20.25238025,20.55916443,20.8094365,21.01606926,21.18852319\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.223391688,3.880934371,4.564460582,5.255520173,5.939697837,6.60662024,7.249462087\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,2.962418597,3.550975666,4.173706503,4.814251643,5.458766988,6.096446145,6.719457473\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.045634362,3.638314936,4.263852678,4.906076561,5.551280392,6.188774771,6.810836836\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.318435729,3.969732746,4.645113239,5.326988062,6.00164683,6.659220507,7.293204019\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,2.895009382,3.413119423,3.955392286,4.512957715,5.07740251,5.641411229,6.199059933\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,4.148235265,4.816939866,5.474461228,6.113263198,6.728213832,7.315996988,7.874668228\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,1.883702233,2.373245096,2.922035773,3.51396722,4.133116585,4.765451753,5.399583393\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.300393255,3.890163081,4.507710731,5.138099824,5.768926577,6.390632199,6.996370306\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.540463587,4.034887459,4.558951953,5.103914917,5.66061051,6.220659017,6.777101614\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.658098409,4.183158096,4.73495518,5.3036052,5.879459573,6.454146773,7.021029898\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.220513805,3.878323004,4.562109732,5.253407898,5.937782023,6.604838242,7.247732839\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,2.960063923,3.54853004,4.171179312,4.811659204,5.4561292,6.093783897,6.71679081\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.047512451,3.640417443,4.266145767,4.90852116,5.553835391,6.191399565,6.813493069\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.318858514,3.970352737,4.645861935,5.327813129,6.00250955,6.660092998,7.294066686\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,2.886460024,3.404307626,3.946407763,4.503890908,5.068337407,5.63242141,6.190207078\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,4.145865572,4.815180519,5.473212869,6.112428489,6.727705421,7.315740352,7.874601723\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,1.884505133,2.374359884,2.923409361,3.515546266,4.134851294,4.767297796,5.401502641\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.301051385,3.890787767,4.508319362,5.138703679,5.769531503,6.391239768,6.996979043\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.536031388,4.030886954,4.555340494,5.100652306,5.657658679,6.217982356,6.774667315\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,3.654399083,4.180186708,4.732584045,5.301726158,5.877982447,6.452997463,7.02014828\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,2.936181423,3.532447795,4.162486568,4.809902209,5.460845112,6.104561712,6.733322519\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.471423351,10.23061292,10.96454401,11.67079627,12.34720902,12.99213557,13.60454345\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.188892752,9.915555314,10.62891285,11.32423057,11.99722937,12.64441589,13.26321481\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,7.456139493,8.256891005,9.044604438,9.815357261,10.56528962,11.29080893,11.98884092\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.137189548,9.86637321,10.58162497,11.2786558,11.95338684,12.60239145,13.22309383\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,7.441242279,8.228894049,9.007791675,9.773067939,10.51999123,11.24425549,11.94223913\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.498325208,10.24850857,10.97620507,11.67805776,12.35130989,12.99393163,13.60463991\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,7.147374725,8.042705599,8.932690484,9.804370958,10.6474277,11.4543848,12.22038673\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,6.511880292,7.276423651,8.036175275,8.78644085,9.522915941,10.24164222,10.93911212\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.083572667,9.803315495,10.51654201,11.21682464,11.89818911,12.55571206,13.18572745\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,6.993186516,7.716785131,8.439964605,9.158802805,9.86880179,10.56535241,11.24415957\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.420642278,10.25813745,11.07236125,11.85407236,12.59695637,13.29731515,13.95356456\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.458818525,10.21933117,10.95435642,11.66153457,12.33874318,12.98436058,13.5973713\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.184942749,9.911584009,10.62491981,11.32023257,11.99324953,12.64047788,13.25933994\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,7.465669785,8.265893542,9.053128549,9.823437194,10.57295109,11.29807306,11.99572655\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.137692203,9.866856533,10.58206379,11.27904071,11.95371682,12.60266969,13.22332538\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,7.438304482,8.226472107,9.005791824,9.771412942,10.51861809,11.24311307,11.94128603\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.497733469,10.24873627,10.97705049,11.67936488,12.35295696,12.9958233,13.60670145\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,7.143776062,8.039131658,8.929133572,9.80083713,10.64393052,11.4509405,12.21701111\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,6.523468662,7.285136597,8.042642605,8.791144821,9.526235237,10.24387765,10.94050342\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.084812028,9.803692314,10.5162415,11.21599959,11.89696451,12.5541892,13.18398768\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,6.991253193,7.715181665,8.438466296,9.157272355,9.86716153,10.56356482,11.24221347\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.409873439,10.24838043,11.06338611,11.8457278,12.58914145,13.28996082,13.94662171\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,9.261989429,10.01632654,10.75022595,11.45991923,12.14209613,12.79422241,13.41462521\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,10.08880724,10.86648453,11.61533551,12.33473793,13.02322721,13.67926065,14.30164995\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,11.92048554,12.83342416,13.66190907,14.41365387,15.09569962,15.71454885,16.27622616\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,10.09442484,10.87211027,11.62085668,12.34007065,13.02831521,13.68407082,14.30616705\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,11.91800675,12.83219711,13.66157566,14.41394362,15.09641367,15.71554313,16.2773973\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,11.11488741,11.90381411,12.64918859,13.35231257,14.01456472,14.63725777,15.22168428\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,13.69468595,14.50812003,15.2373399,15.89445818,16.4892391,17.02959478,17.52199973\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,13.71693822,14.48859897,15.18994389,15.82934638,16.41373999,16.94890957,17.43974584\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,14.93912028,15.57399132,16.15646195,16.69320726,17.18904252,17.6476702,18.07211831\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,13.40590115,14.1723999,14.87511038,15.5213106,16.1164753,16.66501272,17.17068583\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,14.03882405,14.81248369,15.5083056,16.1371462,16.70779139,17.22738962,17.701816\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,13.78633943,14.5479449,15.24100189,15.87351967,16.45215671,16.98248557,17.46923035\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,14.75339792,15.41389167,16.0170276,16.57069507,17.08056953,17.55097711,17.98540759\n\"linker [O-]C(=O)CC(C(=O)[O-])N, n1cc(cc(c1)c1ccncc1)c1ccncc1, nodes [Ni], topology \",,,13.48252733,14.23749829,14.93114786,15.57009535,16.15935767,16.70302044,17.20461543\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,19.56988934,20.02538479,20.38878357,20.68276341,20.92358955,21.12312087,21.29013968\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,19.54287819,20.0032112,20.3704768,20.66755065,20.91085999,21.11239314,21.2810344\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,19.57393057,20.04523409,20.41734039,20.71574927,20.95841732,21.15823151,21.32460686\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,4.326814937,4.909190224,5.508356286,6.113430772,6.714987769,7.305689646,7.880366033\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.455114012,3.951877946,4.485352784,5.043667773,5.615331408,6.190367353,6.7608023\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.911383825,4.421513119,4.962627812,5.523959897,6.094886381,6.66619457,7.230613298\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,4.265088005,4.840579056,5.436808385,6.041847317,6.645252823,7.238828146,7.816738171\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.934015239,4.498387786,5.086681444,5.687132786,6.289275157,6.884733882,7.467388973\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.440437911,3.952945213,4.500184492,5.070153903,5.651373979,6.234012392,6.810325109\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,5.501927446,6.466502542,7.371757357,8.20624546,8.966607814,9.654377773,10.2737861\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,1.901592113,2.344630095,2.847002855,3.399148436,3.990574976,4.610985502,5.250910024\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,4.40724089,4.988386766,5.585674705,6.188439008,6.787410361,7.375363773,7.947210432\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.485027086,3.974158154,4.500549301,5.05258586,5.618907132,6.189570947,6.756573667\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.566726735,4.064078532,4.596340114,5.152387054,5.721223639,6.29321879,6.860649148\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.872501279,4.409993395,4.975697969,5.55809321,6.14648081,6.731980127,7.307848387\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.997379491,4.577773072,5.178455455,5.787916087,6.396062452,6.994923491,7.578769014\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,3.574002472,4.093442314,4.645128392,5.217497652,5.799499775,6.381692591,6.956672839\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,5.559996544,6.530543198,7.438627621,8.273598191,9.032804396,9.718346725,10.33488111\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,1.804819455,2.22105895,2.700814762,3.236373013,3.818027924,4.435425267,5.078466016\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,6.715642328,7.558127107,8.392785712,9.212151474,10.01010396,10.78168476,11.52305242\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,8.66586091,9.415407446,10.162391,10.90223243,11.62856304,12.33501477,13.0161687\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,10.11607677,10.94538223,11.74227223,12.50034027,13.21573214,13.88666729,14.51295438\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,8.607733378,9.340620047,10.07203772,10.79774423,11.51170051,12.20774399,12.880517\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,9.601887502,10.45735044,11.2823824,12.06912955,12.81278845,13.51098419,14.1631768\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,8.329038757,9.158706193,9.971265015,10.76346216,11.53092154,12.26932764,12.97511015\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,9.701388268,10.56051932,11.3873733,12.17477973,12.91822075,13.61545506,14.26603325\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,7.028836678,7.815958686,8.594004083,9.358304339,10.10470367,10.82944395,11.52927053\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,6.74017385,7.532488315,8.319843101,9.095793339,9.855002293,10.59296928,11.30598785\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,6.688046213,7.53328796,8.371148446,9.193987043,9.995491789,10.77054076,11.51517292\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,8.568212907,9.329204783,10.08561877,10.83325819,11.56608833,12.2780148,12.96383497\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,10.17624665,11.00780698,11.80613962,12.5648227,13.28009378,13.95030392,14.57539783\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,8.733301075,9.471233327,10.20768602,10.93805192,11.65594208,12.35495657,13.02962773\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,9.607917703,10.45841306,11.27982405,12.06407739,12.80607343,13.50316964,14.15461959\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,8.336583121,9.169994647,9.983911217,10.77581628,11.54195608,12.27848358,12.98215488\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,9.908929597,10.76800184,11.59129428,12.37264728,13.10841041,13.79702094,14.43853013\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,7.098340686,7.874474837,8.640678168,9.392902798,10.12753397,10.84121956,11.53096949\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,6.678603532,7.473007286,8.26445123,9.045892138,9.81142506,10.5560735,11.27576654\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,14.51464015,15.25506502,15.92184766,16.52564298,17.07467603,17.57545194,18.0332539\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,12.36642972,13.34057252,14.23008563,15.04021439,15.77648331,16.44459339,17.05026841\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,16.02632285,16.86465801,17.58348218,18.20392005,18.74251922,19.21245423,19.6243645\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,14.52638806,15.24673361,15.90677286,16.51166786,17.06607713,17.57424162,18.0400499\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,14.94928232,15.60642762,16.20648352,16.75676908,17.2627755,17.72882803,18.1584945\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,15.2410719,15.89399455,16.48716286,17.02774608,17.52151457,17.97328787,18.3872075\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,13.83199471,14.64875954,15.38551305,16.05203993,16.65653486,17.20591751,17.70609287\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,14.53015586,15.27790507,15.94971925,16.55689835,17.10812019,17.61020878,18.06867492\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,12.4124279,13.37870896,14.26174313,15.06656279,15.79849941,16.46308166,17.06588407\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,15.95685088,16.80212582,17.52706317,18.15283662,18.69608144,19.17006801,19.58552554\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,14.20950923,14.96158919,15.64888725,16.27771578,16.85338,17.38052143,17.86331026\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,14.59678579,15.30562035,15.94980625,16.53790752,17.07635867,17.57024162,18.0237582\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,15.1949763,15.83885983,16.42545637,16.96150972,17.45246931,17.90287667,18.31661851\n\"linker [O-]C(=O)[C]1C[C](C[C](C1)C(=O)O)C(=O)[O-], nodes [Ni][OH][Ni][OH][Ni], topology lim,pcu\",,,13.92644652,14.71694574,15.43218925,16.08124982,16.67165409,17.2097372,17.70090897\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,21.59459827,21.78989781,21.94215441,22.06304092,22.16055594,22.24031884,22.30636584\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,21.59348274,21.78890029,21.94126644,22.06225049,22.15985078,22.23968769,22.3057988\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,17.88103775,18.63372223,19.25507172,19.77162906,20.20424607,20.56923354,20.87936444\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,17.88145004,18.63432818,19.25577012,19.77236127,20.20497826,20.56994657,20.88004798\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,4.333158976,5.125417586,5.886184124,6.605187621,7.278090226,7.904154754,8.484672607\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.102893184,3.758560913,4.423408844,5.083145592,5.728252978,6.352937958,6.954125628\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.52695867,4.203029407,4.898070525,5.59472377,6.279678097,6.94356747,7.580434258\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.550305587,4.208081794,4.888546614,5.574237309,6.25139284,6.91008797,7.54382246\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.221837957,3.856159251,4.517330828,5.188519887,5.855979459,6.509381425,7.141591453\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,4.367505451,5.15686743,5.914966811,6.631457996,7.301992439,7.925842171,8.504308895\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.148435099,3.802921582,4.466689489,5.125299456,5.769173829,6.392505688,6.992228281\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.52014438,4.196364826,4.891703807,5.588741818,6.274122259,6.938448002,7.575741719\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.551235012,4.209283045,4.890030594,5.575984088,6.253364514,6.912238943,7.546106335\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.217586494,3.852244204,4.5137932,5.185369788,5.853206096,6.506961424,7.139494966\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,4.373114816,5.162829573,5.921076127,6.637560585,7.307979002,7.931639122,8.5098699\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.148319495,3.802945125,4.466788427,5.125427177,5.769298141,6.392605848,6.992292231\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.520562848,4.196898281,4.892333288,5.589447417,6.274884745,6.939249948,7.576568091\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.551526682,4.209817106,4.89077691,5.576907165,6.254427933,6.913408321,7.547350975\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.21735991,3.852164272,4.513870134,5.185598454,5.853571912,6.507445065,7.140075654\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,4.331629264,5.124010892,5.884857503,6.603913499,7.276852194,7.902944047,8.483485402\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.104381705,3.760423286,4.425556967,5.085500311,5.730746136,6.355512499,6.956734746\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.526454646,4.202558204,4.897637322,5.594330057,6.279322988,6.943248698,7.580148872\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.550372707,4.208232196,4.888777686,5.574540569,6.251756978,6.910500882,7.544272485\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,3.221869781,3.856257201,4.517493981,5.188744356,5.856258925,6.509708076,7.141956901\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,7.626860497,8.369468285,9.110175966,9.845023502,10.5689316,11.27669086,11.96360549\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.521524236,10.31514242,11.07695438,11.80520429,12.49869531,13.15674451,13.77916405\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.683872678,10.44649182,11.18293035,11.89092524,12.56850088,13.21416301,13.82698959\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.10362358,8.849999823,9.588729705,10.31692562,11.03054714,11.7253199,12.39735067\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.90164311,9.679952032,10.4392237,11.17466745,11.88243539,12.55966534,13.20444797\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.875776985,7.692405196,8.493705725,9.274990868,10.03281728,10.7645198,11.46802953\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.931341754,7.708974789,8.48016453,9.238762863,9.980030106,10.70015558,11.39606707\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,7.624087491,8.365555191,9.1052226,9.839162477,10.56231092,11.26946048,11.95590807\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.536064285,10.32803304,11.08832067,11.81518405,12.50742913,13.16436931,13.78580893\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.688292817,10.44954315,11.18480477,11.89180924,12.56856483,13.21355743,13.82584479\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.107625337,8.852994479,9.590669797,10.31785252,11.03055128,11.72451487,12.3958568\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.885989757,9.665651663,10.42606637,11.16249153,11.87111389,12.54909709,13.19455127\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.889132664,7.699628149,8.496028547,9.273421461,10.02818359,10.75750224,11.45918596\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.916812416,7.696230718,8.468275131,9.227099577,9.968202058,10.68794934,11.38339474\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,7.62561055,8.367574091,9.107688519,9.842011136,10.56547132,11.27286181,11.95948433\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.534916528,10.32716127,11.08767371,11.81472021,12.50711404,13.16417451,13.78571088\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.684503732,10.44612787,11.18173361,11.8890508,12.56608775,13.21133164,13.82384228\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.107551561,8.853360351,9.591451671,10.31900393,11.03201477,11.72623048,12.3977674\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.887227986,9.666807762,10.42716023,11.16353298,11.87210757,12.55004517,13.19545488\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.894102294,7.703759943,8.499576604,9.276560957,10.03103565,10.76015034,11.46168708\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.916862726,7.696000614,8.467880599,9.226618719,9.967686495,10.68743227,11.38289663\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,7.628813124,8.371253496,9.11183659,9.846587261,10.57041581,11.27810605,11.96495805\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.521056338,10.31473289,11.07660957,11.80492391,12.49847548,13.15657954,13.77904753\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.683864181,10.44648649,11.18295489,11.89099014,12.56860801,13.21430978,13.82717134\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.105084794,8.851411124,9.590140448,10.31835918,11.03201073,11.72681125,12.39886251\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,8.897772498,9.676326037,10.4358169,11.17146075,11.87941367,12.55681598,13.20175992\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.875169936,7.691838454,8.493190433,9.274534337,10.03242315,10.76418862,11.46775957\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,6.940435143,7.71621795,8.485973638,9.243447566,9.983825987,10.70324454,11.39859096\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.096790446,9.9957024,10.85673926,11.67711537,12.45508744,13.18977595,13.88105722\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.048201058,9.950710204,10.8150135,11.6383399,12.4189754,13.15607368,13.84954278\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.046620628,9.949194989,10.81358848,11.63701659,12.41775681,13.15495761,13.84852398\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,9.097316303,9.996317814,10.85741121,11.67781735,12.45579909,13.19048224,13.88174756\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,13.01134801,13.97530781,14.85042309,15.64312842,16.36014157,17.0081721,17.59371135\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.35115814,16.08108322,16.72002973,17.28501202,17.78912507,18.24246649,18.6528571\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.3695288,16.06819716,16.69244017,17.25415135,17.76248964,18.22461554,18.64622697\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.41654664,16.11675259,16.74544404,17.31305432,17.82778951,18.29618776,18.72355585\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,19.44512974,19.97568653,20.4017056,20.7497996,21.03875551,21.28207634,21.48963456\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,13.3256408,14.25988448,15.10873108,15.87814315,16.57445711,17.20406237,17.77317463\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.53363466,16.23998192,16.85973987,17.40891612,17.89985323,18.34208661,18.74301459\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.75580176,16.40345876,16.98577696,17.51265083,17.99176347,18.4291632,18.82969544\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,14.74204112,15.52331587,16.21926604,16.84322011,17.40560599,17.91466989,18.37703772\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,20.12276193,20.55264934,20.89824231,21.18126059,21.4169317,21.6161415,21.78681424\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,13.35165353,14.28336893,15.13008753,15.8976765,16.59240478,17.22061379,17.78848467\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.64561069,16.33696061,16.94458293,17.48380874,17.96648698,18.40178838,18.7968384\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.78004742,16.42435696,17.00402722,17.52876439,18.00612228,18.44205843,18.84135333\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,14.76653503,15.54483064,16.23833789,16.86026402,17.42094574,17.9285609,18.38968405\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,20.10031902,20.53352447,20.88177301,21.16694226,21.40437575,21.60504521,21.7769391\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,13.0176736,13.98092513,14.85545435,15.64766808,16.36426315,17.01193364,17.59715939\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.34523613,16.07616736,16.71593465,17.28159169,17.78626282,18.24006807,18.65084568\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.40951811,16.10191172,16.72123478,17.27901978,17.78417563,18.24368628,18.6631225\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,15.53961305,16.22450685,16.84072568,17.39801175,17.90408126,18.3651176,18.78616555\n\"linker [O-]C(=O)c1ccc(cn1)C(=O)[O-], nodes O, [Ni], [Sr], topology pcu\",,,19.42375297,19.95738771,20.38588595,20.7359976,21.02661301,21.27131283,21.48002809\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,17.81831929,18.32411964,18.73608821,19.07496481,19.35635021,19.59207578,19.79119369\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,17.51934526,18.06904548,18.51592131,18.88288581,19.18713643,19.44168252,19.65645244\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,2.774718183,3.387153777,4.036444582,4.704341628,5.375645643,6.038738897,6.685420027\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.064988507,3.724812889,4.407188152,5.094524685,5.773050529,6.432851969,7.06742583\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.616416285,4.308577996,5.014748657,5.718189874,6.406311987,7.070435619,7.705198854\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.793145727,4.502745277,5.212681536,5.908778104,6.58069405,7.221492407,7.827013191\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,2.806925705,3.421357259,4.072116739,4.740963758,5.41274672,6.075915039,6.7223401\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.061334381,3.715696286,4.392156802,5.073619266,5.74663733,6.401474211,7.031691919\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.557670053,4.243813578,4.945627604,5.646274436,6.332974588,6.996830711,7.632269676\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.553812851,4.25178369,4.955631658,5.650221312,6.324252705,6.969920031,7.582321785\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.75739307,4.307808564,4.805524756,5.250280372,5.645000779,5.99409462,6.302452536\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,3.007206622,3.538422999,4.039232813,4.502801856,4.926658479,5.311110384,5.658086007\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,9.211170509,10.03209025,10.820723,11.57433856,12.29095684,12.96939348,13.60923331\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,8.035928982,8.798748459,9.535104645,10.24250283,10.91902565,11.56335399,12.17476155\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,9.150367773,9.988727175,10.79877164,11.57489139,12.31321389,13.0114251,13.66852535\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,7.545509607,8.348141668,9.12744515,9.877496809,10.59412003,11.27462848,11.91757749\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,9.226069493,10.04192193,10.82594943,11.57556882,12.28885398,12.96460864,13.60236531\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,7.86919213,8.627194637,9.358644458,10.0613138,10.73353161,11.37414633,11.98251333\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,9.14785049,9.988884446,10.80127835,11.57943638,12.3195068,13.01919842,13.67753563\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,7.332625583,8.106572587,8.857212942,9.580008204,10.27176031,10.93036956,11.55465175\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,7.652064865,8.435452091,9.213112991,9.979751085,10.72956722,11.45716733,12.15807256\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,6.262094774,7.05335047,7.841982757,8.621195233,9.385338409,10.12963423,10.85012434\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,7.735970835,8.436628684,9.130367089,9.815853562,10.49026705,11.15015668,11.79206769\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,6.214682828,6.986684993,7.752427162,8.506885271,9.246019564,9.9663423,10.66481628\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,7.65686087,8.443023315,9.222558892,9.990364656,10.74082033,11.4686806,12.1695825\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,6.269897485,7.074191696,7.877989443,8.67318912,9.453077131,10.2120993,10.94579665\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,7.77875884,8.527250378,9.267498424,9.99634281,10.70969407,11.40338321,12.07369933\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,6.246396931,7.045458647,7.843853518,8.633551031,9.407967156,10.16170202,10.890442\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,13.79347402,14.61395246,15.35312256,16.0201893,16.6234002,17.1699858,17.6662285\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,13.88579582,14.70067468,15.42904192,16.0826765,16.67154401,17.20397418,17.68691158\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,14.09122866,14.93192954,15.6808044,16.35067552,16.95208742,17.49375715,17.98295804\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,14.43081092,15.21863182,15.91546165,16.53636208,17.09311537,17.59500121,18.0494083\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,13.8249831,14.64832617,15.39117836,16.06207662,16.66886745,17.2185605,17.71733661\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,13.81906803,14.65394252,15.40968608,16.09346509,16.71226478,17.27260241,17.78042874\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,13.93653637,14.782116,15.53579762,16.21030415,16.81619439,17.36223112,17.85572952\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,13.38019339,14.26887673,15.05938638,15.76563493,16.39922022,16.96975199,17.48520577\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,14.86317358,15.87536444,16.7324404,17.45955423,18.07850861,18.60764055,19.06212465\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [OH], topology pcu\",,,14.7299151,15.74248327,16.60123785,17.33095065,17.95311221,18.48581261,18.94403948\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,19.29819309,19.72307599,20.06036809,20.33205935,20.55380396,20.73693681,20.88980054\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,19.86759353,20.20689441,20.47446931,20.68888554,20.86316108,21.00660998,21.12602223\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,19.08834211,19.51647549,19.85632161,20.1300369,20.35340167,20.53784498,20.69177965\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,19.9035426,20.31464633,20.63979283,20.90090091,21.11346447,21.28863743,21.43458949\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,5.478840548,6.22514838,6.940902573,7.621334444,8.263287133,8.86510318,9.426401262\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,3.677906924,4.358119971,5.047143044,5.730605345,6.397968836,7.042046069,7.658412477\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.839436786,3.458252069,4.104364786,4.762172492,5.419101458,6.065735467,6.695526559\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.655306266,3.27013802,3.920497566,4.5882992,5.258594514,5.919974951,6.564365284\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.126908685,2.584784151,3.099925888,3.661073041,4.255945069,4.872935589,5.501979192\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,1.927686055,2.430994014,2.990299086,3.58910873,4.212034516,4.846056426,5.480917594\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,3.258405717,3.898823468,4.561120632,5.229196651,5.890582082,6.536282933,7.160316399\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.869963269,3.483182792,4.124379257,4.778020506,5.431453138,6.075100917,6.70222938\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,3.106664298,3.754917121,4.427639991,5.107827418,5.781950603,6.440047741,7.075361931\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.026978286,2.496287378,3.023488249,3.596644643,4.203114873,4.831130065,5.470571718\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.449138726,3.044781414,3.681193365,4.339811671,5.005088253,5.664995559,6.310875187\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,5.554935636,6.235048938,6.89438597,7.527991263,8.132091132,8.704123463,9.242665421\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,3.006700224,3.645630331,4.306297418,4.973600152,5.635632833,6.283657215,6.911744995\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.696158371,3.314870121,3.967325051,4.635697995,5.305349193,5.965162188,6.607309338\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.046955388,2.520582484,3.051613671,3.627528643,4.235291334,4.862937361,5.50032551\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.231547814,2.810733641,3.436739427,4.090408228,4.755354782,5.418679529,6.070924255\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,3.037370558,3.666210388,4.322284235,4.988608763,5.651868168,6.302345056,6.933471275\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.692423281,3.271517214,3.885421923,4.518665368,5.158112154,5.793457958,6.417169489\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.692814602,3.295541637,3.934975982,4.593338346,5.255708443,5.910547165,6.549574081\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,2.075708613,2.536904987,3.056057199,3.621640591,4.221200033,4.843010524,5.47692102\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.055851777,9.890590469,10.68714837,11.445412,12.16505458,12.8457924,13.4876032\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.399380368,10.16234113,10.90831858,11.63117765,12.32592711,12.98891366,13.61779488\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.831997394,9.636789928,10.4128352,11.1584484,11.87173722,12.5510926,13.19544638\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.857720615,9.68438281,10.48280904,11.24986501,11.98268415,12.67909054,13.33776678\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.932245023,9.579339865,10.20989912,10.82558462,11.42651014,12.0117326,12.57977368\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.172270854,9.964933241,10.72255238,11.44634358,12.13661967,12.79331167,13.41634227\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.704777574,10.4544747,11.18618157,11.8951753,12.57725859,13.22916941,13.84870218\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.075716379,9.858375908,10.61175498,11.33507057,12.02715163,12.68689578,13.31353735\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.043895229,9.815222037,10.55666368,11.26799454,11.94854794,12.59759667,13.21460636\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.362515786,9.044392044,9.712491822,10.3657901,11.00250584,11.62048262,12.21757213\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.031489356,9.818604435,10.57597672,11.30269613,11.99748144,12.65914876,13.28688927\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.394314996,10.17636817,10.93859125,11.6748092,12.38023772,13.05148974,13.6864781\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.82869515,9.638725746,10.41851367,11.16670233,11.88170085,12.5621409,13.20713221\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.797941762,9.594853809,10.36185289,11.09815391,11.80253567,12.47381291,13.11113307\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.20668548,8.879505124,9.539290407,10.18467564,10.81379994,11.42456443,12.01492732\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.159495713,9.993961276,10.79189198,11.55260605,12.27533716,12.959546,13.60510986\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.716752129,10.447966,11.15932168,11.84778639,12.51036465,13.14455423,13.74855674\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.135349671,9.891299937,10.61794593,11.31561482,11.98392014,12.6222568,13.23011799\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.988503526,9.775701468,10.53529884,11.26584204,11.9656135,12.63308457,13.26717628\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,8.719364928,9.382517452,10.0310905,10.66522776,11.28397924,11.88571815,12.46857933\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,10.21470159,11.03773124,11.82586685,12.57783629,13.29207762,13.96733607,14.60296137\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.893277323,10.75410708,11.58130718,12.37130039,13.12103218,13.82844067,14.49256717\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,10.39009494,11.24548176,12.05985126,12.83257991,13.56278478,14.24989915,14.89393748\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,10.08392594,10.90837853,11.70365837,12.46633783,13.19321282,13.88187556,14.53091649\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,10.06451542,10.89931471,11.69836604,12.46034837,13.18365842,13.86704473,14.50990186\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,9.972073459,10.79412879,11.58124197,12.3326286,13.0470246,13.72333392,14.3609567\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,10.31322911,11.15537146,11.96075624,12.72810469,13.45581068,14.14262345,14.78796502\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,10.17198081,11.00728707,11.81233864,12.58326741,13.31668038,14.01017032,14.66244987\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,15.37099374,15.98872813,16.55368209,17.07276294,17.55080737,17.99147374,18.39775738\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,16.23192172,16.76581256,17.2430306,17.67562075,18.07170492,18.43684935,18.77496842\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,14.80397266,15.45175477,16.04656088,16.59310261,17.09503633,17.55554933,17.97762643\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,15.35589597,15.93153097,16.44387578,16.90568137,17.32586831,17.7107683,18.06498259\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,14.36842464,15.00162424,15.58603655,16.12514114,16.62166722,17.07813702,17.49707476\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,15.69259558,16.22098554,16.69351927,17.12179275,17.51377886,17.87503483,18.20951655\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,15.34580391,15.97950647,16.56229903,17.09922361,17.59397809,18.0496033,18.46883235\n\"linker [O-]C=O, n1ccncc1, nodes [Ni], topology dmp\",,,15.73521191,16.26715663,16.74234161,17.17273927,17.56647256,17.92914145,18.26470484\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,19.83545185,20.09630359,20.30232968,20.46763339,20.60213282,20.71294367,20.80526477\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,19.84365092,20.10450602,20.31053456,20.47584019,20.6103412,20.72115337,20.8134756\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.508223414,4.164447317,4.840538718,5.52013345,6.190447088,6.842283034,7.469614284\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.635559241,4.271859292,4.926454608,5.584661132,6.234832251,6.868432298,7.479732632\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.545673247,4.184975526,4.843983885,5.507568946,6.163669625,6.803417489,7.42084265\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,2.908350611,3.518630094,4.160795058,4.818199771,5.476953465,6.12636923,6.758835087\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.552585797,4.192944189,4.851268239,5.512917912,6.166287961,6.802876642,7.416979943\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.554122027,4.208501597,4.88211882,5.558872315,6.226185239,6.875010715,7.49942157\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.516469873,4.157395842,4.816585293,5.479326688,6.133948413,6.771893663,7.387415782\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.009874304,3.632991606,4.285377592,4.950329218,5.614106054,6.26628498,6.899564975\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.52152621,4.16153819,4.821598461,5.486459733,6.143954552,6.785131789,7.403963559\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.680663152,4.31524781,4.967516815,5.623040698,6.270375611,6.901133077,7.509682758\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.314227208,3.982410417,4.675558533,5.375102114,6.066387804,6.738834696,7.385500433\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.541647443,4.197327286,4.872493527,5.550891477,6.219836845,6.870215142,7.496061904\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.315069581,3.98406204,4.678105522,5.3785604,6.070715517,6.743950872,7.391302641\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.541536433,4.195667317,4.869072806,5.545672204,6.212891543,6.861671315,7.486061915\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.553859706,4.208221204,4.881825631,5.558571226,6.225880622,6.874706388,7.499120833\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.517442005,4.158442227,4.817682873,5.480455113,6.135090455,6.773035147,7.388545288\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.010317587,3.63347931,4.28589847,4.950872815,5.614663221,6.266848041,6.900127698\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.521348982,4.161312794,4.82133594,5.486170574,6.143648046,6.784815786,7.403644475\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.681119201,4.315717485,4.967991867,5.623514437,6.27084281,6.901589764,7.510125979\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.508246424,4.164475217,4.840571568,5.520170823,6.190488174,6.842326762,7.469659418\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.634576755,4.270842657,4.925417962,5.583616239,6.233788737,6.867397913,7.478713504\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.544375976,4.183604133,4.842565131,5.506125891,6.162221456,6.801979743,7.419427611\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,2.908307369,3.518564085,4.160709163,4.81809721,5.476837433,6.126242699,6.758700719\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.553064427,4.193441948,4.851774703,5.51342453,6.166788022,6.803365093,7.417453143\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.314403071,3.982602923,4.675762937,5.375314301,6.066604351,6.739052847,7.385718036\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.541617719,4.197296085,4.872462851,5.55086268,6.219810782,6.870192309,7.496042555\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.315010582,3.984007262,4.678056225,5.378517215,6.070678596,6.743920034,7.391277502\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,3.541619155,4.195760765,4.869175057,5.545781371,6.213005848,6.861789146,7.486181858\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.820484319,7.574611175,8.327737174,9.073566589,9.806764384,10.52272659,11.21755745\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.763643278,8.554584441,9.329005189,10.08503569,10.82007554,11.53128007,12.21599145\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.308805736,10.09203957,10.85465124,11.59151283,12.29849113,12.97264319,13.61217535\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.776382403,10.5423144,11.28001836,11.98743851,12.66301693,13.30570622,13.91497457\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.720708277,10.4952214,11.23918464,11.95114903,12.63003516,13.27515515,13.88623966\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.546580678,10.34015074,11.09697762,11.81755217,12.50217158,13.15110539,13.76474178\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.602789755,10.38183043,11.12984256,11.84552818,12.52788332,13.17626284,13.79042382\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.83324375,7.572822268,8.312764743,9.047423667,9.771699353,10.48093497,11.17101154\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.755448988,8.535379148,9.298850157,10.04444487,10.76991155,11.4726328,12.15006531\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.322085148,10.09577529,10.85021588,11.58015282,12.28133531,12.9507042,13.58635065\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.56626382,10.34851935,11.09894127,11.81648589,12.50033258,13.14996396,13.76522342\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.521970592,10.31658975,11.07467991,11.79660569,12.48258829,13.13285372,13.747766\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.66930077,10.44678766,11.19299231,11.90670684,12.5870135,13.23333204,13.84546416\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.771579771,10.53522309,11.27111798,11.9771232,12.65160708,13.29346181,13.90210673\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.229911221,10.00729788,10.76208209,11.49043918,12.18910062,12.85564146,13.4885371\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.537509515,8.377296825,9.200744301,10.00342541,10.78130295,11.53082808,12.24911793\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.714958377,8.513611966,9.303982635,10.08120202,10.84008576,11.57578589,12.2842239\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.672878154,8.455277018,9.231563075,9.996631477,10.74517772,11.47226109,12.17369653\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.647439706,8.431542438,9.209661181,9.976577222,10.72690403,11.45564797,12.15859452\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.723230898,8.522950642,9.314407711,10.09266365,10.85248031,11.58897482,12.29805114\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.564180236,8.40395325,9.227389747,10.03005183,10.80789368,11.55736142,12.27557038\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.344256319,10.12385178,10.88372287,11.61856302,12.32409085,12.99724086,13.63611905\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.804772986,8.5909576,9.360933414,10.1129509,10.84448339,11.55271654,12.23498789\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.247406601,10.02736602,10.78422451,11.51427868,12.21434866,12.88207341,13.51597452\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.800068503,8.58340997,9.350217019,10.09896415,10.82729877,11.53253077,12.21207724\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.343609141,10.11915866,10.87552111,11.60730605,12.31017894,12.98103647,13.61795301\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.866714244,7.608834678,8.351793634,9.089759696,9.81743875,10.53001235,11.22324516\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.850656441,7.603289439,8.354883272,9.099016442,9.830329931,10.54424989,11.23693437\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.833488832,7.573097619,8.313059866,9.047731751,9.772015995,10.48125739,11.17133803\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.755223585,8.535147465,9.298614024,10.04420618,10.76967191,11.47239343,12.1498271\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.321705784,10.09538922,10.84982528,11.57975953,12.28094068,12.95030916,13.58595576\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.566549161,10.34883501,11.0992917,11.81687283,12.50075567,13.1504213,13.76571213\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.522849206,10.31747201,11.07556936,11.79750466,12.48349793,13.13377418,13.74869669\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.670217355,10.44765579,11.19382142,11.90750556,12.58778929,13.23409115,13.84621167\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.771878085,10.53551686,11.27141307,11.97742336,12.65191442,13.29377723,13.90243029\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.821086664,7.57519055,8.328304857,9.074131321,9.807332564,10.52330267,11.21814436\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.763699374,8.554647043,9.329075477,10.08511487,10.82016441,11.53137894,12.21610017\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.308637108,10.09184056,10.85442508,11.59126336,12.29822224,12.97235855,13.61187825\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.776355282,10.54225134,11.27992074,11.98730932,12.66285995,13.30552545,13.91477394\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.721443063,10.4959219,11.23985305,11.95178901,12.63065091,13.2757509,13.88681935\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.546985484,10.34051301,11.09730312,11.81784667,12.50244051,13.15135366,13.76497374\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.602825494,10.38185142,11.12984994,11.84552335,12.5278678,13.17623821,13.7903916\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.229992474,10.00741492,10.76222981,11.49061331,12.18929732,12.85585719,13.48876855\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.537251581,8.377028918,9.200469551,10.00314631,10.7810213,11.5305451,12.24883435\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.715188441,8.513846567,9.304221245,10.08144441,10.84033167,11.57603492,12.28447546\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.674004216,8.456378984,9.232645668,9.997699479,10.74623548,11.47331228,12.17474414\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.64834386,8.432403599,9.210488562,9.977379139,10.72768761,11.4564191,12.15935795\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.723306526,8.523007445,9.314451041,10.09269777,10.85250847,11.58899937,12.29807378\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.563967509,8.403718132,9.227139705,10.02979296,10.80763067,11.55709772,12.27530842\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.344348149,10.12391056,10.88375392,11.6185711,12.32408013,12.99721493,13.63608096\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.805100343,8.591262423,9.361216002,10.11321251,10.84472588,11.55294211,12.23519885\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.24736954,10.02731965,10.78416942,11.51421613,12.21428009,12.88200028,13.51589811\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,7.800371421,8.583706607,9.350507089,10.09924799,10.82757674,11.53280311,12.21234397\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,9.343595965,10.11915964,10.87553395,11.60732915,12.31021096,12.98107615,13.61799912\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.867490497,7.609631517,8.352609114,9.090593358,9.818290557,10.53088221,11.22413279\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,6.851530423,7.604249608,8.355914797,9.100107426,9.831470641,10.54543234,11.23815203\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,14.57650284,15.35848236,16.06914292,16.71449238,17.30042125,17.83249981,18.31589363\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,16.09820358,16.68282776,17.21086532,17.6910525,18.13003526,18.53296274,18.90390458\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.52234193,16.17920971,16.77344773,17.31343611,17.80579959,18.25589384,18.66814873\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.01838275,15.74935023,16.40747004,17.00239797,17.54189103,18.03231386,18.47899757\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.37460722,16.06733696,16.6924904,17.25913873,17.77438644,18.24397828,18.67269767\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.10862846,15.82152506,16.46492353,17.0479442,17.57797398,18.06108192,18.50233546\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,14.71028809,15.49163636,16.20056393,16.84339599,17.42624538,17.9548451,18.43448551\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,16.04794869,16.62011157,17.13819326,17.61020812,18.0423899,18.43963782,18.80585436\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.52167692,16.17870129,16.77307423,17.3131805,17.805648,18.25583464,18.66817197\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.01765088,15.74883322,16.40712881,17.00220461,17.54182471,18.03235844,18.47914011\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,14.57917863,15.36109248,16.07170184,16.7170109,17.30290749,17.83495987,18.31833214\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,16.09915677,16.68377604,17.21181427,17.69200558,18.13099448,18.53392919,18.90487873\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.37424462,16.06698756,16.69215781,17.25882523,17.77409321,18.24370564,18.67244532\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,15.10826745,15.82159623,16.46534443,17.04865341,17.57892444,18.06223666,18.50366487\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,14.71240011,15.49387206,16.20293549,16.84590667,17.42889295,17.95762406,18.4373886\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1ccc(cc1)c1ccc(cc1)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology nbo\",,,16.05015806,16.62228671,17.14032757,17.61230163,18.04444592,18.44166108,18.80784997\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.13674592,20.55477624,20.88895549,21.15964497,21.38155616,21.56547903,21.7194417\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,19.89579939,20.34556095,20.70617869,20.99897617,21.23947112,21.43910853,21.6064419\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.11196533,20.53367812,20.8708051,21.14388433,21.36775565,21.55330353,21.7086266\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,19.90320842,20.35187499,20.71160923,21.00368742,21.2435913,21.4427385,21.60966168\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,20.27106238,20.68831641,21.01727204,21.28066114,21.49450045,21.67028683,21.81641785\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,5.656247329,6.634031309,7.547953462,8.387561221,9.150239868,9.838115077,10.45590593\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,4.025345188,4.622365789,5.246734092,5.882166961,6.515213196,7.135721797,7.73668061\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.859220042,4.436885289,5.045916679,5.67002831,6.295478986,6.911657105,7.511018517\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.957520657,4.544001353,5.161287713,5.792421516,6.423348827,7.043397091,7.6451177\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.986839892,4.571765735,5.184807904,5.81008518,6.434420907,7.047783804,7.643149875\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,5.6527948,6.630618379,7.544647083,8.384401815,9.147248793,9.835300723,10.45326827\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,4.024130942,4.621327825,5.245831903,5.881372151,6.514505613,7.135086979,7.736108089\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.859366459,4.436971573,5.045956553,5.670032919,6.295457391,6.911616741,7.510965564\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.957503034,4.544005814,5.161310151,5.792458514,6.423397532,7.043455129,7.645183106\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,3.986237916,4.571211128,5.184285658,5.809587012,6.433942461,7.047322923,7.642705569\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.874913711,7.620363708,8.366164492,9.106458986,9.835968085,10.54989592,11.2440336\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.36657177,11.05680554,11.72687906,12.37384317,12.99522834,13.58923958,14.15476379\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.915662531,7.668263025,8.419431517,9.163842109,9.896522026,10.61285127,11.30872983\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.37590627,11.05964294,11.72479941,12.36820695,12.98715009,13.57959417,14.14421285\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.908501867,7.642147887,8.37684027,9.107099849,9.827834891,10.53429785,11.22223661\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.51218503,11.1629193,11.79971634,12.4189227,13.01736381,13.59257179,14.14281582\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.917320546,7.649680006,8.381042125,9.10706689,9.823371555,10.52562448,11.20979505\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.35531188,11.02874245,11.68579905,12.32265906,12.9362318,13.52427028,14.08532092\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.874062565,7.619805449,8.365821924,9.106280331,9.835916465,10.54994373,11.24415943\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.36190824,11.05291751,11.72358685,12.37101756,12.99277464,13.58708719,14.15285912\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.918512447,7.670513857,8.421217097,9.165264839,9.897660774,10.61376703,11.30946988\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.37597105,11.05956576,11.72464016,12.368004,12.98692728,13.57936594,14.14398772\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.906137662,7.640389587,8.375554748,9.106184094,9.827208065,10.53389612,11.22200951\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.51066799,11.16149151,11.7983752,12.41766324,13.0161802,13.59145809,14.1417664\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,6.916167754,7.64868959,8.38015464,9.106244804,9.822591876,10.52487364,11.20906545\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,10.3528108,11.02659883,11.6839259,12.32099528,12.93473398,13.52290715,14.08406954\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,16.57509414,17.55261682,18.36217039,19.03697202,19.60336095,20.08208489,20.48948291\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,15.30080627,16.00728861,16.64295204,17.21701629,17.73718607,18.20988479,18.64049267\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.57342649,15.34892843,16.04992418,16.68483676,17.26084028,17.78414231,18.26017273\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,15.09533104,15.84619596,16.51537956,17.11531206,17.65579647,18.14466716,18.58828319\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.42954126,15.20012572,15.900403,16.53752783,17.11771315,17.64645169,18.12865152\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,15.0749501,15.80583283,16.46209454,17.05360887,17.58864913,18.07411264,18.51576556\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.40965543,15.19645791,15.91086726,16.55978222,17.14945779,17.68558671,18.17334602\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.06659482,14.88044227,15.61687968,16.28435906,16.89014938,17.44061138,17.94136465\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.97307125,15.7044548,16.36331055,16.95929157,17.50015186,17.99224279,18.44086947\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,16.55881518,17.53801103,18.34907635,19.02522045,19.59279114,20.07255139,20.48085737\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,15.22078868,15.93776079,16.58202795,17.16323273,17.68938961,18.16715396,18.6020828\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.58388133,15.35876669,16.05903422,16.69319879,17.26848202,17.79111386,18.26653267\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,15.11254228,15.86166217,16.52933945,17.12796411,17.6673066,18.15517498,18.59790695\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.50073751,15.26382408,15.95758574,16.58903985,17.1642791,17.68869203,18.16709728\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,15.01736024,15.75501019,16.41696604,17.01330854,17.55247191,18.04147992,18.48619897\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.4131584,15.19965443,15.91371601,16.56228369,17.15163382,17.68746861,18.1749679\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.02515682,14.84250301,15.58221793,16.25271429,16.86125021,17.41419282,17.91717759\n\"linker [O-]C(=O)C=CC(=O)[O-], nodes [Zn][OH]([Zn][OH]([Zn])[Zn])[Zn], topology pcu\",,,14.96283231,15.69585017,16.35600903,16.95303757,17.49474757,17.98753411,18.43673544\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,17.73927271,17.94117649,18.09996501,18.22693511,18.32996177,18.41465377,18.4850844\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,18.1794963,18.38651548,18.54937686,18.67963743,18.78535697,18.87227824,18.94457341\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.25500928,3.906192494,4.580330519,5.260441119,5.933125429,6.588640035,7.220503373\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.495563953,4.156075887,4.836248889,5.519383729,6.192485074,6.846247734,7.474612237\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.275117547,3.927957655,4.606018989,5.291443904,5.970136081,6.631858336,7.269813897\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.317785358,3.967508642,4.642364586,5.324735313,6.00068069,6.660051797,7.296090343\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.11670525,3.753060066,4.41929564,5.09722384,5.772165705,6.433223376,7.072961942\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.261192926,3.91165231,4.588017376,5.272355816,5.950454815,6.611946169,7.249906588\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.387915494,4.045429028,4.723934261,5.406649082,6.080434943,6.735813806,7.366546904\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.493980085,4.156672022,4.837599884,5.520330139,6.192133493,6.843936274,7.469865147\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.321945508,3.97825717,4.659067562,5.346502618,6.026512598,6.688939433,7.327077522\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.348565753,4.001596722,4.67873627,5.362449085,6.038922624,6.698148295,7.333502486\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.113337006,3.748982838,4.414925085,5.092912999,5.768201167,6.429828328,7.07030298\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,3.239500175,3.892132167,4.570454802,5.256463797,5.935918909,6.598456495,7.237177504\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,7.835310986,8.555610154,9.274827244,9.988831099,10.69248398,11.38058697,12.04848956\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,8.854283051,9.628793946,10.37557893,11.09201936,11.77625146,12.42707182,13.04388233\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.243565433,10.01069348,10.75292771,11.46681535,12.14986315,12.80040699,13.41751892\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,6.285542202,7.079425171,7.871760454,8.655056486,9.423255153,10.17134958,10.89526366\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,7.659019906,8.389144139,9.118162007,9.841631248,10.55423002,11.25066435,11.92624902\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.244080006,10.01557395,10.75991399,11.47446563,12.15729071,12.80709414,13.42318968\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.41086779,10.18480998,10.93202247,11.64954291,12.33521768,12.98762112,13.60599858\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,6.179007491,6.925180701,7.677631487,8.428622181,9.171279815,9.899558076,10.60832542\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,7.804779989,8.517339757,9.229121082,9.936377608,10.63422104,11.31758078,11.98183936\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.337970212,10.10138176,10.83866707,11.54712034,12.22473791,12.87015097,13.48259216\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.404970704,10.17404096,10.91753125,11.63226302,12.31593801,12.96701746,13.58464768\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,6.073631989,6.806665191,7.547274198,8.28788632,9.021691228,9.742613214,10.44542521\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,7.795155658,8.515186826,9.234717957,9.949360359,10.65381443,11.34277928,12.01154124\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.217156032,9.994404456,10.74424242,11.46379877,12.1510449,12.8046774,13.42404404\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,8.86517941,9.63150208,10.37312342,11.08646608,11.76898464,12.41899896,13.03558109\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,6.276604722,7.06504107,7.852275404,8.630815425,9.394639867,10.13878088,10.8591872\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,7.752965903,8.477828903,9.201921664,9.920858768,10.62934626,11.32209533,11.99440925\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.378916336,10.15026073,10.89490796,11.60999648,12.29344052,12.94385085,13.56048444\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.312448717,10.08245292,10.82627628,11.54090182,12.22413685,12.87452254,13.49127086\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,6.524792736,7.263710702,8.009846092,8.755357349,9.493284113,10.21749875,10.9227921\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,7.841967933,8.554898473,9.266945604,9.974399584,10.67238917,11.35585281,12.02017908\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.502842149,10.26782031,11.00632074,11.71569377,12.39398942,13.03988483,13.65265066\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.225295386,9.995641018,10.73996314,11.45522835,12.13923444,12.79050826,13.40824156\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,6.410267341,7.149055521,7.893526547,8.636551855,9.371709574,10.09324567,10.79618624\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,15.14055838,15.81345042,16.41648521,16.96048141,17.45372307,17.90267263,18.31249005\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,14.72082313,15.48489306,16.16451773,16.77314173,17.3211652,17.81675653,18.26645675\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,14.29314561,15.0927194,15.81078485,16.45756316,17.04169268,17.57049011,18.05019061\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,10.81028219,11.47767056,12.08280418,12.63262701,13.13309926,13.5893438,14.00579974\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,14.7818161,15.53429491,16.212368,16.82472873,17.37892553,17.88147126,18.33799079\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,9.172109234,9.85634541,10.47812947,11.0434697,11.55792961,12.02653109,12.45376723\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,15.35578166,16.01576507,16.60833938,17.14376765,17.62994572,18.07305032,18.4780221\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,15.29805135,15.96765396,16.56800528,17.10978657,17.6011482,18.04844316,18.45675108\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,14.65549346,15.32344972,15.93011268,16.4819532,16.98466227,17.44321315,17.86196332\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,14.7533058,15.5184278,16.20723868,16.8287475,17.39075423,17.89997881,18.36221935\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,13.42807027,14.12586242,14.75795642,15.33138896,15.85242349,16.32655566,16.758596\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Gd], topology pcu,dia\",,,14.39293237,15.19994916,15.92489817,16.57772259,17.16699065,17.70005728,18.18324578\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,18.6597795,19.24057563,19.71617976,20.10922199,20.43690414,20.7123848,20.94580595\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,18.6118722,19.19899595,19.67984782,20.07727088,20.4086343,20.68722864,20.92330031\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,2.227257547,2.860179643,3.540529225,4.245743147,4.956883134,5.659386162,6.342909182\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,2.24784085,2.884748672,3.568413486,4.276226518,4.989303703,5.693194139,6.377691568\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,4.67436267,5.426995261,6.16913207,6.887417666,7.573208641,8.221615039,8.830589777\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,3.885835615,4.64410899,5.405785818,6.153077378,6.873755682,7.560270115,8.208713559\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.911498414,7.728058445,8.536740702,9.331843109,10.1081891,10.861176,11.58694478\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.682781429,7.511462843,8.332830361,9.140528387,9.929030534,10.69355938,11.43017953\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.629907436,7.44724826,8.256767103,9.052951178,9.830868827,10.5861117,11.31493023\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.674915439,7.511122334,8.334708905,9.14090903,9.925570135,10.68498476,11.41599096\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.950126074,7.764600453,8.569980834,9.361106408,10.13321299,10.88198762,11.60375881\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.663754251,7.494864066,8.317838572,9.126509718,9.915529682,10.68027331,11.41692508\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.636880645,7.454121144,8.263432853,9.059343439,9.836951523,10.5918702,11.32036427\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,6.684933057,7.517874382,8.33828011,9.141558639,9.923644779,10.68086147,11.41004166\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,8.612036201,9.587963632,10.53021698,11.42985294,12.28127153,13.08151345,13.82962862\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,9.490013158,10.35407502,11.18619894,11.98144889,12.73601789,13.44752528,14.11496413\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,8.648492956,9.622280099,10.56253637,11.46030968,12.30998708,13.108597,13.85517948\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,9.517888365,10.37374923,11.19925598,11.98916758,12.7394454,13.44752687,14.11225812\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,7.449171217,8.319976627,9.175743604,10.00852522,10.81232568,11.58279397,12.31699333\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,9.489410396,10.20328115,10.90733945,11.59522946,12.26166743,12.90259448,13.51514985\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,7.339406159,8.220506236,9.084697691,9.923979777,10.73258406,11.50650216,12.24315232\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,9.299365197,10.08859993,10.85273376,11.58866169,12.29346289,12.96486082,13.60139296\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,19.06803518,19.71333525,20.24268061,20.68016851,21.04458722,21.35052504,21.60932298\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,19.04707477,19.69579907,20.22780807,20.6674058,21.03352214,21.34084483,21.60078633\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,17.89380414,18.64465524,19.27154436,19.79767949,20.24186776,20.61918576,20.94167624\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,17.99016141,18.72234054,19.33506267,19.8502988,20.28598861,20.65659417,20.97371797\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.6407446,11.49460448,12.29916518,13.05698497,13.76957823,14.43809407,15.06370477\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.52723303,11.42255084,12.26768326,13.06323434,13.80953427,14.50717556,15.15723209\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.0760079,10.96185777,11.80311325,12.59937138,13.35008581,14.05508853,14.7147966\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.21987899,11.09109678,11.91807118,12.70093956,13.43940529,14.13338482,14.78328478\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.61165291,11.4663706,12.27118925,13.02888313,13.74115865,14.40931041,15.0346085\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.47340135,11.3694553,12.21525406,13.01152797,13.75867825,14.45732585,15.10854404\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.13990122,11.02417139,11.86277344,12.65571208,13.40275832,14.10397617,14.75994263\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,10.26054765,11.126307,11.94729188,12.72408719,13.4567093,14.14527494,14.79030221\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,14.02986835,14.94844002,15.76314638,16.48743321,17.13307945,17.71021172,18.22747912\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,14.47961654,15.32975617,16.08545928,16.75952575,17.36276966,17.90427113,18.39167334\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,13.56401862,14.54069133,15.40604359,16.17409195,16.85737727,17.46681781,18.01181127\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,13.57049392,14.5100992,15.34611016,16.09149694,16.75773127,17.35474483,17.89106731\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,13.92989839,14.8634376,15.69001779,16.42381134,17.07715422,17.66059273,18.18309011\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,14.36174441,15.21769439,15.97967858,16.66007499,17.26946647,17.81681583,18.30971449\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,13.67139281,14.63505535,15.48911892,16.24743388,16.92234611,17.52458355,18.06337138\n\"linker O=C1[N]C(=NC(=O)[CH]1)SSC1=NC(=O)[CH]C(=O)[N]1, nodes [Mn], topology rna\",,,13.50142082,14.44864078,15.29211507,16.04442979,16.71688978,17.31938609,17.86047583\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,22.40150139,22.66234732,22.86466802,23.02455466,23.15298039,23.2576186,23.34395626\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,22.4043622,22.66474244,22.86670076,23.02630032,23.15449504,23.25894475,23.34512671\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,22.402433,22.66312656,22.86532887,23.02512184,23.15347228,23.2580491,23.34433609\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,22.40531863,22.66554249,22.86737931,23.02688272,23.15500015,23.25938685,23.34551679\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.234492038,3.881010664,4.553222226,5.233691302,5.908583751,6.567781214,7.204496889\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.582459356,4.242048007,4.92045857,5.60134404,6.272054418,6.923578198,7.55008172\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.336754864,3.986068666,4.657752665,5.335213776,6.005347788,6.658597434,7.288573312\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.409636523,4.058737862,4.730096669,5.407064869,6.076526067,6.728950723,7.35800449\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.406402483,3.911083234,4.451932851,5.017208692,5.595434711,6.176624695,6.752805346\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.43287813,3.945310615,4.492131311,5.062025379,5.643906207,6.228123848,6.80698709\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.484945998,4.020047585,4.586934204,5.173499407,5.768344747,6.361850473,6.946566604\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.352496357,3.868851239,4.420526207,4.995376278,5.581724186,6.169535239,6.750888282\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.233990756,3.880477609,4.552669178,5.23312872,5.908020259,6.567223553,7.203950098\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.582202279,4.241773985,4.920174051,5.601055008,6.271765829,6.923293865,7.54980441\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.335755729,3.985009096,4.656653994,5.334095166,6.004225405,6.6574843,7.287479526\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.410512407,4.059691286,4.731107325,5.408113646,6.077596019,6.730027469,7.359076247\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.407424393,3.912048179,4.452843664,5.018068092,5.59624533,6.177389083,6.753525967\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.433718463,3.946092832,4.492857351,5.062698826,5.644531906,6.228707521,6.807534995\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.484873808,4.020056241,4.587011435,5.173633511,5.768524784,6.362066464,6.946809667\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.351862029,3.868236804,4.419933016,4.994806345,5.581179422,6.169017127,6.750397798\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.23399367,3.880459704,4.552637015,5.23308748,5.907973801,6.567174631,7.203900605\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.581792872,4.241329524,4.919710159,5.600583902,6.271296593,6.922832975,7.549356282\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.33623792,3.98551823,4.657181628,5.334633247,6.004766781,6.658022953,7.288010605\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.410003334,4.05913202,4.730510559,5.407491265,6.076958536,6.7293838,7.358433706\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.406673943,3.911335529,4.45216857,5.017429771,5.595642497,6.176820057,6.752988796\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.43328838,3.945729367,4.492557039,5.062454466,5.644333425,6.228542813,6.807390699\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.484982747,4.020123044,4.587047005,5.173646013,5.768520332,6.362049636,6.946783884\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.35201359,3.8683353,4.419986986,4.994823306,5.581166008,6.16897914,6.750340237\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.233965365,3.880441153,4.552627322,5.233085672,5.907978829,6.567185412,7.203916078\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.581443286,4.240957567,4.919325275,5.600194436,6.270909278,6.922452897,7.548987078\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.335842264,3.985128752,4.656803697,5.334270661,6.004421958,6.657697197,7.287704375\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.410227572,4.059379747,4.730778827,5.407776464,6.077256741,6.729691101,7.358746447\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.407312765,3.911943988,4.452746507,5.01797764,5.59616133,6.177311349,6.753454365\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.433548623,3.94592022,4.492683967,5.062526819,5.644363436,6.228544694,6.807379829\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.48476292,4.019895559,4.586807496,5.173393872,5.768257169,6.361778205,6.946507389\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.352193376,3.868582803,4.42029041,4.995171221,5.581547722,6.169384995,6.750761779\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.234547357,3.881076843,4.553296994,5.233772468,5.908669334,6.567869498,7.204586434\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.582277928,4.241854185,4.920256231,5.601136771,6.271845318,6.923369821,7.549876093\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.336727382,3.986045714,4.657734017,5.335199069,6.005336589,6.658589293,7.28856779\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.409522481,4.058608112,4.729954982,5.406914775,6.076370663,6.728792611,7.357845783\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.406601004,3.91126646,4.452103119,5.017367766,5.595583772,6.176764421,6.752936018\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.433359651,3.945822824,4.492669113,5.062581045,5.644470091,6.228685033,6.80753397\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.485088757,4.020236385,4.587166364,5.173769808,5.768646952,6.362177588,6.946911862\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.351991602,3.868301132,4.419941697,4.994768298,5.581102868,6.168909492,6.750265633\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.234075759,3.880567245,4.552761512,5.233222101,5.908113357,6.567315334,7.204039788\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.582001294,4.241554667,4.919941828,5.600814832,6.271521933,6.923049708,7.549562713\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.335809967,3.985074009,4.656727524,5.334175251,6.004310145,6.657572038,7.287568864\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.410439593,4.059614873,4.731028982,5.408034787,6.07751777,6.729950684,7.359001546\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.40726218,3.911893634,4.452696168,5.017927338,5.596111258,6.177261812,6.753405731\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.433561871,3.945944531,4.492718069,5.062569719,5.644414635,6.228604283,6.807448484\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.484806878,4.019965834,4.586899991,5.173504266,5.768381311,6.361912349,6.946648297\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.352226262,3.868641136,4.420370055,4.99526795,5.581657562,6.169504415,6.750887759\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.234248413,3.880756828,4.552967678,5.233442969,5.908346196,6.567557094,7.204287454\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.581717878,4.241225967,4.919583031,5.600438284,6.271137222,6.922664025,7.549181295\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.336644046,3.985944064,4.657619113,5.335075349,6.005207702,6.658458111,7.288436503\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.409750151,4.058869073,4.730243202,5.40722392,6.076694669,6.729126008,7.358183857\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.406521037,3.911187232,4.452022863,5.017285573,5.595499498,6.176678514,6.752849333\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.433034022,3.945470199,4.492293925,5.062189805,5.644070906,6.228287145,6.807147308\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.484806465,4.019905836,4.586791827,5.173357805,5.768205113,6.361713795,6.946433689\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.352574117,3.86895576,4.420655317,4.995526651,5.581891924,6.169716326,6.751078891\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.234011188,3.880496843,4.552690957,5.233155279,5.908052587,6.567261746,7.203993683\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.581552035,4.241077571,4.919453796,5.600328799,6.271047082,6.922592108,7.549126044\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.335830097,3.98510979,4.656778178,5.334239176,6.00438531,6.657656275,7.287660066\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.410136548,4.059279029,4.73067145,5.407665062,6.077143491,6.729577737,7.358634308\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.407446461,3.912079084,4.452882154,5.018112823,5.596295016,6.17744259,6.753582347\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.433551198,3.945904634,4.492651293,5.062478871,5.644302493,6.22847325,6.807300402\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.48477538,4.019908721,4.586820433,5.173405914,5.768267857,6.36178724,6.94651458\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,3.352060822,3.868431019,4.420121584,4.994988328,5.581354051,6.16918381,6.750556104\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.692485109,10.46886722,11.21805418,11.93736141,12.6247161,13.27870232,13.8985564\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.78073499,10.53560887,11.26843759,11.97533171,12.65324025,13.29999769,13.91428136\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081340458,8.825651303,9.562433968,10.28913478,11.00198373,11.69684077,12.36982653\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.591502432,10.36323321,11.1091692,11.82637091,12.51257216,13.16620841,13.78639367\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.711289309,10.46540303,11.19709758,11.90273849,12.57948215,13.22530854,13.83898124\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.21734396,8.951172953,9.678240394,10.3964097,11.10193886,11.79054638,12.45816103\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.40755333,11.36606345,12.27087507,13.11480883,13.8954885,14.61367599,15.27205422\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.44255803,11.40646314,12.31340629,13.15727313,13.93648354,14.652359,15.30796002\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.692628665,10.46907769,11.21831779,11.93766711,12.62505475,13.27906626,13.89893913\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.78025454,10.53519342,11.26807487,11.97501324,12.65295985,13.29975053,13.91406352\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081181794,8.825553887,9.562385803,10.28912532,11.00200403,11.69688343,12.36988558\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.591156418,10.36294375,11.10892428,11.82616242,12.5123943,13.16605682,13.78626482\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.711905072,10.46602068,11.19771574,11.90335563,12.58009652,13.22591826,13.83958441\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.217591375,8.951440924,9.678533724,10.39673083,11.10228781,11.79092123,12.45855857\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.4078676,11.36636399,12.27117253,13.11510835,13.8957918,14.61398287,15.2723635\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.44178703,11.40579663,12.31281164,13.1567293,13.93597715,14.65188164,15.30750637\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.6925229,10.46890217,11.21808584,11.93738959,12.62474073,13.27872343,13.8985741\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.78049381,10.53536599,11.26819413,11.97508908,12.65299985,13.2997607,13.91404878\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081366253,8.825687074,9.562478408,10.28918636,11.00204085,11.69690189,12.36989026\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.591233844,10.36299056,11.10894572,11.82616165,12.51237356,13.16601801,13.78620983\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.711368317,10.46548599,11.1971853,11.9028307,12.57957801,13.22540697,13.83908112\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.21736043,8.951188714,9.678258455,10.39643218,11.10196697,11.79058063,12.45820136\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.40758681,11.36607728,12.27087607,13.11480166,13.89547623,14.61366057,15.27203677\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.44245831,11.40634526,12.31327695,13.15713767,13.93634594,14.65222214,15.30782585\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.692494417,10.46894714,11.21819553,11.93755584,12.62495574,13.27897973,13.89886467\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.780043883,10.53497168,11.26784458,11.97477719,12.65272067,13.29951054,13.91382465\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081234087,8.825597745,9.562421456,10.28915337,11.0020253,11.69689882,12.36989599\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.591229046,10.36304808,11.10906116,11.82633057,12.51259099,13.16627845,13.78650743\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.711964035,10.4660816,11.19777857,11.90342027,12.58016275,13.22598578,13.83965286\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.217528837,8.951392631,9.678497355,10.39670427,11.10226917,11.79090892,12.45855126\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.40807102,11.36658077,12.27139595,13.11533343,13.89601501,14.61420177,15.27257646\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.44152877,11.40552729,12.31253963,13.15646051,13.9357155,14.65162961,15.30726541\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.692441782,10.46884759,11.21805588,11.93738192,12.62475285,13.27875281,13.89861829\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.780674982,10.53554864,11.26837567,11.97526753,12.65317383,13.29992937,13.91421165\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081384644,8.825701944,9.562489432,10.2891937,11.00204496,11.69690332,12.3698896\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.591319979,10.36307098,11.10902678,11.82624745,12.51246642,13.16611897,13.78631896\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.711271468,10.46538248,11.19707571,11.90271648,12.5794609,13.22528867,13.83896313\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.217301326,8.951132427,9.678203279,10.39637691,11.1019109,11.79052342,12.45814299\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.40770895,11.3662176,12.27102753,13.11495875,13.89563479,14.61381754,15.27218994\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.44258841,11.40646086,12.31337903,13.15722732,13.93642433,14.65229044,15.30788522\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.692647555,10.46909105,11.21832661,11.93767215,12.62505665,13.27906553,13.89893622\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.780262631,10.53519073,11.26806092,11.97498836,12.65292492,13.29970674,13.91401215\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081162911,8.825534311,9.562365553,10.28910453,11.00198289,11.69686216,12.3698644\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.59115656,10.36295492,11.10894718,11.82619698,12.51243986,13.16611232,13.78632898\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.711893019,10.46601234,11.19771008,11.90335195,12.58009435,13.22591727,13.83958436\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.217578904,8.951433558,9.678530385,10.39673055,11.10228976,11.79092474,12.45856311\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.40792708,11.36643422,12.27124955,13.11518935,13.89587487,14.61406671,15.2724473\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.44194891,11.40597408,12.31299899,13.15692191,13.9361714,14.65207478,15.30769642\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.692402941,10.46880812,11.21801604,11.93734183,12.62471257,13.27871235,13.8985777\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.780610098,10.53545471,11.26825924,11.97513418,12.65302815,13.29977506,13.91405167\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081402613,8.82571978,9.562508276,10.28921393,11.0020665,11.69692589,12.36991283\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.591527521,10.3632615,11.10920135,11.82640699,12.51261181,13.1662511,13.78643877\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.711337014,10.46546581,11.19717344,11.90282514,12.57957726,13.22540995,13.83908704\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.217365606,8.951195082,9.678265793,10.39644023,11.10197549,11.79058941,12.45821022\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.40739323,11.36588746,12.27069101,13.11462236,13.89530357,14.61349526,15.27187937\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.44231355,11.40621761,12.31316403,13.15703736,13.93625642,14.65214186,15.30775356\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.69248387,10.46893672,11.21818578,11.93754714,12.62494832,13.27897372,13.8988601\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.78006146,10.53499281,11.26787074,11.97480904,12.65275831,13.29955366,13.91387268\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.081223997,8.825583083,9.562401787,10.28912875,11.00199611,11.69686563,12.36985947\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.591196665,10.36300626,11.10900995,11.82627051,12.51252297,13.16620355,13.78642682\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,9.712000912,10.46610546,11.19779082,11.90342236,12.58015613,13.22597181,13.8396328\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,8.217555443,8.951412223,9.678509435,10.39670885,11.10226665,11.79089996,12.45853664\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.40799321,11.36649495,12.27130547,13.11524076,13.89592194,14.6141096,15.27248612\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,10.4414392,11.4054407,12.31245629,13.15638056,13.93563903,14.65155662,15.30719586\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.46734433,19.17303136,19.77152331,20.28168157,20.71875422,21.09509946,21.42076028\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.46792031,19.17352483,19.77194753,20.28204787,20.71907207,21.09537675,21.42100349\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.46718731,19.17286076,19.7713477,20.28150654,20.71858331,21.09493481,21.42060306\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.46797589,19.17358779,19.77201433,20.28211601,20.71913986,21.09544306,21.42106762\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.4673013,19.17296526,19.77144303,20.2815933,20.7186622,21.09500656,21.4206684\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.46809557,19.17370088,19.77212025,20.28221466,20.71923145,21.09552795,21.42114626\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.46714394,19.17283608,19.77133649,20.28150495,20.71858851,21.09494472,21.42061619\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,18.46793016,19.17354362,19.77197199,20.28207568,20.71910164,21.09540698,21.42103365\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,23.22592699,23.31437176,23.38209898,23.4350851,23.47730402,23.5114792,23.53952655\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,23.22445965,23.313153,23.38107095,23.43420651,23.47654465,23.51081642,23.5389431\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,23.22590172,23.31435073,23.38208122,23.4350699,23.47729086,23.51146771,23.53951643\n\"linker S1Cc2ccc(cc2)CSCc2ccc(C1)cc2, nodes [Cu]Br, topology \",,,23.22442097,23.31312073,23.38104364,23.43418311,23.47652437,23.51079869,23.53892748\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,20.37032066,20.82115998,21.18005355,21.46984864,21.70686298,21.90295541,22.06688574\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,20.27238878,20.73793761,21.10856658,21.40784899,21.65262707,21.85514367,22.02444372\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,20.26302755,20.73004663,21.10183179,21.40203852,21.64756626,21.85069864,22.02051023\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,20.3500551,20.80406486,21.16545631,21.45725028,21.69588663,21.89331182,22.05834957\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.209147908,3.822947716,4.464354478,5.117434202,5.768998061,6.408975259,7.030259607\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.119468283,3.718876282,4.349691906,4.995673397,5.643176488,6.281640456,6.903496499\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.215604931,3.829675852,4.471171861,5.124208771,5.7756367,6.415414715,7.03645911\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.341242728,4.011569153,4.704702368,5.40240795,6.09059912,6.759269052,7.401952153\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,1.909300465,2.39653221,2.937306926,3.51936306,4.131013842,4.761936927,5.403430413\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,1.907451347,2.394691548,2.935456402,3.51749538,4.129129645,4.76004174,5.401532242\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,1.919281876,2.409637783,2.953100345,3.53723279,4.150257795,4.78183626,5.423305525\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.116633082,3.715932031,4.346703445,4.992691431,5.640238807,6.278773937,6.900719255\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.337558915,4.007422886,4.700160587,5.397552606,6.085515436,6.7540377,7.396644886\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.119398495,3.718684402,4.349405788,4.995317762,5.642772243,6.281204599,6.903042413\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.116474204,3.715800873,4.346593079,4.992597548,5.640158515,6.278705132,6.9006603\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,1.917770146,2.4081283,2.951576627,3.535687062,4.148688523,4.780245791,5.421698285\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.340574318,4.010811864,4.703882867,5.401549574,6.089721251,6.758387113,7.401077963\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.337944046,4.007785666,4.700509585,5.397891994,6.085846869,6.754361476,7.396960639\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.209204001,3.822994828,4.464397845,5.117476913,5.769041663,6.409020303,7.030306059\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,3.216049802,3.830093534,4.471568048,5.124585194,5.77599358,6.415751928,7.036776674\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.715977112,8.507975867,9.28919008,10.05588823,10.80375114,11.5285697,12.22670973\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.638920344,10.41523767,11.15980938,11.87197125,12.55100495,13.19636574,13.80782154\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.642260771,10.41796834,11.16201548,11.87373926,12.55241342,13.19748214,13.80870204\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.773739634,7.546292399,8.3146349,9.072507557,9.814915564,10.53770629,11.23744061\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,8.967311816,9.730348747,10.47699312,11.20258969,11.90299124,12.57487851,13.21587468\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.71935662,8.511748583,9.293287172,10.06024619,10.80831059,11.53327544,12.23151133\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.611465968,7.421590054,8.225218519,9.015500736,9.78712989,10.53584828,11.25826137\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.321057291,10.04715179,10.7598438,11.45507454,12.12871547,12.77718925,13.39775406\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.315390403,8.138070402,8.952216264,9.751372008,10.52971687,11.2823401,12.00539298\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.601849168,7.413054923,8.217490651,9.008368074,9.780433138,10.52947199,11.2521252\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.607338596,7.41819162,8.222356373,9.013041304,9.784978893,10.53393814,11.25654298\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.322713903,8.143437657,8.955962032,9.753763735,10.53097686,11.28265774,12.00493141\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.604213882,7.415005198,8.219132471,9.009772303,9.781649227,10.5305358,11.25306359\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.318938619,10.04519542,10.75790878,11.45308125,12.12662606,12.77499276,13.39545578\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.323342482,10.04916959,10.76161952,11.45663316,12.13008148,12.7783859,13.39880281\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.742526799,7.52121353,8.294525557,9.056404218,9.802028831,10.52739592,11.22919169\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.323201927,8.143840802,8.956258652,9.753947292,10.53105051,11.28263028,12.00481449\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.717478099,8.510075587,9.29177745,10.05887285,10.80705521,11.53212438,12.23045375\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.63529988,10.41172003,11.15645906,11.86882506,12.54807932,13.19366326,13.80533597\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,8.970051471,9.732923577,10.47940106,11.20483155,11.90507158,12.57680484,13.21765636\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.647472299,10.42300156,11.1668223,11.87828862,12.55668981,13.20148218,13.81243096\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.314259372,8.137127795,8.951455483,9.75077948,10.52927543,11.28203128,12.00519849\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,9.316861196,10.0432421,10.75609561,11.45141484,12.12510572,12.77361285,13.3942076\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.741243723,7.520509429,8.294229528,9.056398486,9.802230309,10.52774488,11.22964456\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,8.96971459,9.732199782,10.47855799,11.20403088,11.90440472,12.57631702,13.21736324\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,8.97022616,9.732588283,10.47888437,11.20433371,11.90470668,12.57663022,13.21769295\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,6.774959227,7.547278743,8.315415898,9.07311156,9.815369204,10.53803354,11.23766249\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,7.717166753,8.509168077,9.290346271,10.05698248,10.80476811,11.5295021,12.22755593\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,10.20130585,11.03527855,11.83092316,12.58783301,13.30545319,13.9834248,14.62177688\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,10.20202206,11.03612087,11.8318492,12.58881102,13.30645941,13.98444152,14.62279091\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,10.14576947,10.98554208,11.78618248,12.54739705,13.26873872,13.94994342,14.59112011\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,10.14253678,10.98228583,11.78295282,12.54422986,13.26565908,13.94696812,14.58825965\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.5635772,15.33066207,16.02671841,16.6589968,17.23397646,17.7574176,18.23443742\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,15.34635733,16.03578744,16.65402069,17.21185151,17.71771084,18.1782728,18.59891093\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.6929828,15.46265713,16.15520203,16.7804948,17.34673807,17.86079117,18.32844722\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.51135981,15.2981701,16.0043909,16.64072207,17.2160361,17.73771333,18.21193735\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.94261347,15.67954917,16.33713065,16.92794514,17.46175939,17.94625285,18.38756373\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.77562358,15.53292007,16.21572574,16.83322592,17.39313908,17.90197901,18.3652879\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.52388222,15.29606622,15.99631477,16.6320822,17.20999628,17.73592808,18.21507913\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.50149307,15.27678813,15.97904077,16.61614795,17.19501179,17.72166981,18.2014222\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.93858519,15.6757119,16.3335483,16.92463921,17.45872802,17.94348209,18.38503402\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.50804221,15.48522698,16.31966367,17.03590759,17.65457999,18.192633,18.66385271\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.58917515,15.36778182,16.06680719,16.69684068,17.26664534,17.78349906,18.2534929\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.8275542,15.5777523,16.25483634,16.86765018,17.42367261,17.92924462,18.38978088\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.76176176,15.52093869,16.20518113,16.82380388,17.38461322,17.89418396,18.3581012\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.57180336,15.34823248,16.04623082,16.67597651,17.24596313,17.76329212,18.23393868\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,15.36826506,16.05533497,16.67149868,17.22752207,17.73180481,18.19099082,18.61042612\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.48144465,15.46103137,16.29768494,17.01593702,17.63640949,18.17606703,18.6487134\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.53351114,15.31409984,16.01573072,16.6486436,17.2213909,17.74112834,18.2138797\n\"linker [O-]C(=O)c1cnccc1C(=O)[O-], nodes [Ni][OH2][Ni], topology kgd,\",,,14.6182552,15.37634631,16.06497525,16.69110326,17.26098338,17.78019216,18.25369541\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,21.27586736,21.4168613,21.52685987,21.61424374,21.68476173,21.74245804,21.79024132\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,21.26081412,21.40502179,21.51754383,21.60688671,21.67892314,21.73780001,21.78650594\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,21.2844679,21.42397296,21.53284096,21.61934547,21.68916558,21.74629853,21.79362032\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,21.27079913,21.41332794,21.52455825,21.61288681,21.68411269,21.74233194,21.79049717\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,3.486801566,4.151146256,4.837728156,5.528984606,6.211097995,6.874121345,7.511558483\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,3.359500273,4.037327745,4.733138827,5.430397051,6.116272364,6.78161722,7.420518956\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,3.313075255,3.98053276,4.672014889,5.369347556,6.058254061,6.728452901,7.373208306\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,3.486502015,4.150590813,4.836973572,5.528079135,6.210081987,6.873027965,7.510414535\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,3.357989,4.035758027,4.731563382,5.428852566,6.114783047,6.780197844,7.419177407\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,3.314296245,3.981513029,4.672796973,5.369967115,6.058741004,6.728832176,7.373500576\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.955253823,8.740332025,9.514511558,10.27434939,11.0156848,11.73435166,12.42668748\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,9.442374149,10.21525652,10.96746045,11.69433146,12.39200408,13.05765727,13.68952502\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.927524747,8.710670799,9.478500112,10.22949269,10.96096434,11.66978907,12.35297554\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,9.322065644,10.15877715,10.96617096,11.7398931,12.47660368,13.17416638,13.83158791\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.951022024,8.729294177,9.495862603,10.24779033,10.98137429,11.69280199,12.37864728\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,9.466226059,10.2607604,11.02835981,11.7658113,12.47041652,13.14026723,13.77429745\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.117340827,7.917860441,8.710301069,9.488779083,10.24841716,10.98509659,11.69543686\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.086786154,7.878650889,8.66271136,9.433604865,10.18675904,10.91818736,11.62451542\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.32844045,8.128730565,8.919757849,9.695663372,10.45163795,11.18368496,11.88858474\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.959959718,8.744150185,9.517698796,10.27709001,11.0181096,11.7365522,12.42872686\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,9.446275912,10.21846495,10.97007533,11.69643472,12.39366667,13.05894206,13.69048791\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.922069394,8.705223807,9.47317932,10.22435922,10.95604653,11.66509671,12.34850818\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,9.32240547,10.15851354,10.96550919,11.73897435,12.4755261,13.17299853,13.83037762\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.951643831,8.729399245,9.495590797,10.24723902,10.98061367,11.69188443,12.37761297\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,9.472845214,10.26674052,11.03382788,11.77085996,12.47511356,13.14466252,13.77842813\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.125786143,7.924675927,8.715852751,9.493355153,10.25224301,10.98834671,11.69824496\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.101112006,7.890369478,8.672391773,9.441685127,10.19357901,10.92401107,11.62954773\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,7.341195295,8.138209411,8.926645249,9.700509191,10.45488392,11.18568464,11.88961978\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,22.33669459,22.61455546,22.8316287,23.00412448,23.14328127,23.25705792,23.35120208\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,22.38887525,22.65992383,22.87126051,23.03893698,23.174037,23.28438435,23.3756142\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,22.33227003,22.61095444,22.828641,23.00160554,23.14112855,23.25519675,23.34957677\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,22.391888,22.66255977,22.87357133,23.04097088,23.17583585,23.28598347,23.37704302\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.51222068,16.25299802,16.91495636,17.50926398,18.04485057,18.52896398,18.96759865\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.55704676,16.24417535,16.86033435,17.41564929,17.91841597,18.37537724,18.79203148\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.97877799,16.64430457,17.23535051,17.76525594,18.24380994,18.67834901,19.07451463\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,14.98131983,15.74369902,16.42995457,17.04892531,17.60846689,18.11539408,18.57557563\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,16.59614029,17.15690759,17.65907926,18.11292662,18.52620719,18.9047768,19.25309121\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.5613286,16.32922648,17.01347457,17.62570929,18.17530412,18.66996045,19.11613194\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.55247245,16.28753348,16.94507031,17.53586585,18.06859707,18.55034233,18.9869796\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.57253698,16.25991843,16.87594871,17.43090497,17.93317766,18.38956944,18.80561688\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.97172564,16.63719896,17.22857328,17.75897976,18.23809411,18.6731929,19.06988756\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.21785775,15.95218768,16.61512919,17.21447828,17.75733416,18.24994594,18.69774985\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,16.79748032,17.33086936,17.81102647,18.24690754,18.6453278,19.01145611,19.34923963\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Cd]Cl, [Cd], topology \",,,15.57104573,16.33555167,17.01757467,17.62833546,18.17694513,18.67093797,19.11666006\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,21.82206042,22.01744515,22.16941707,22.28985606,22.38686964,22.46613425,22.53171466\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,21.81732714,22.01272975,22.16471545,22.28516528,22.38218754,22.46145919,22.52704538\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,21.9899865,22.1889426,22.3437578,22.46649122,22.56537924,22.64619238,22.71306516\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,22.12870201,22.32639048,22.48027037,22.60229743,22.70064086,22.78102631,22.84755766\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.7154551,4.422098732,5.142713787,5.859416353,6.55904856,7.232751991,7.875225092\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.736676641,4.441272606,5.159724145,5.874351899,6.572109008,7.244188742,7.885306153\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.685864695,4.391695257,5.111609653,5.82774948,6.52696132,7.200376619,7.842675506\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.726045052,4.430754095,5.14912997,5.863551919,6.56101674,7.232744743,7.873464478\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.695917659,4.401875599,5.122179836,5.838876841,6.538740911,7.212853671,7.855863644\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.733828157,4.438707648,5.15731086,5.87199413,6.56974479,7.241783818,7.882846666\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.712141031,4.418866069,5.139467206,5.856097155,6.555626334,7.229214662,7.871570423\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.735132502,4.440590249,5.159656246,5.874680412,6.572647851,7.244778312,7.885806042\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.715435486,4.422078096,5.142693465,5.859397325,6.559031488,7.23273728,7.875212955\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.736779244,4.44138041,5.159836205,5.874467192,6.572226507,7.244307461,7.885425178\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.685989725,4.391829528,5.111750724,5.827895262,6.527110112,7.200527081,7.842826608\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.725930286,4.43064387,5.149024413,5.86345097,6.560920187,7.232652266,7.873375684\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.695923605,4.401887355,5.122195929,5.838895867,6.538761637,7.212875064,7.855884866\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.733794008,4.438668659,5.157268427,5.871949493,6.569699018,7.241737808,7.88280116\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.712187599,4.418921152,5.139528483,5.856162493,6.555693895,7.229282933,7.871638201\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,3.734978525,4.44042742,5.159488129,5.874510015,6.572477563,7.244609944,7.885640907\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.955328484,9.815362147,10.65533568,11.46906091,12.25119256,12.99761133,13.70553705\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,10.00958179,10.77684522,11.51943247,12.23406337,12.91806515,13.56944366,14.18693526\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.961785839,10.72217769,11.45932625,12.16980939,12.8508137,13.50020194,14.11656795\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.861518354,9.708624384,10.53983445,11.34843039,12.12840751,12.87498493,13.58478841\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.314114149,8.119570449,8.913659889,9.691699727,10.44963112,11.18388613,11.89144474\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.423961419,8.220408976,9.008308427,9.781940143,10.53655765,11.26814095,11.97337884\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.74641352,9.603090879,10.4405748,11.2524244,12.03311419,12.77839699,13.48540269\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.781506881,10.54800236,11.29019444,12.00467948,12.68871339,13.34025666,13.95801359\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.810584734,10.57209719,11.31021622,12.02155427,12.70331863,13.35338533,13.97035746\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.80605623,9.655143976,10.48754518,11.2967202,12.07680322,12.82312483,13.53240123\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.136435912,7.931011282,8.716892128,9.4886764,10.24179532,10.9723118,11.67693525\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.382096511,8.187592692,8.98198694,9.760238964,10.51810407,11.251933,11.95868818\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.936223553,9.795002173,10.6342974,11.4476925,12.22969146,12.97607902,13.68401625\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.96950768,10.73700717,11.47994426,12.1949771,12.87940391,13.5312169,14.1491457\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.905055979,10.66621772,11.40422531,12.11558967,12.79746472,13.44769799,14.0648767\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.81499459,9.661809448,10.49273159,11.30100038,12.08059092,12.82671756,13.53601081\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.355970617,8.154807359,8.943684288,9.717554791,10.47209486,11.20354266,11.90873625\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.315065392,8.115553366,8.906679553,9.682770209,10.43918257,11.17201539,11.87807043\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.922912999,9.781612503,10.62100235,11.43472141,12.21727543,12.96442276,13.67328599\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.946407535,10.71640371,11.46183437,12.17930552,12.86607391,13.52010472,14.1401128\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.919510694,10.68358972,11.42413415,12.13769582,12.8214566,13.47328975,14.0918089\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.897598038,9.740804794,10.56883428,11.37475805,12.15242381,12.89695223,13.60490527\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.32764082,8.130144634,8.921707392,9.697588119,10.45368586,11.18639637,11.89266544\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.429776577,8.225094875,9.01051201,9.781061858,10.53245976,11.26095617,11.9633861\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.955181431,9.815216558,10.6551904,11.46891519,12.25104601,12.99746377,13.70538847\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,10.00965067,10.7769194,11.51951064,12.23414459,12.91814873,13.5695291,14.1870222\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.961984342,10.72238186,11.45953572,12.17002374,12.85103245,13.50042462,14.11679407\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.861460586,9.708564484,10.53977241,11.34836656,12.12834241,12.8749191,13.58472239\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.314086167,8.119553191,8.913652473,9.691701281,10.44964076,11.18390298,11.89146794\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.423660422,8.220122342,9.008034732,9.781678568,10.53630764,11.26790206,11.97315066\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.749164765,9.605850202,10.44334088,11.25519637,12.03589145,12.78117912,13.48818937\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.782393516,10.54892274,11.29114365,12.00565333,12.6897083,13.34126949,13.95904163\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.810363163,10.57190719,11.31005275,12.0214133,12.70319681,13.35327982,13.97026585\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.806181249,9.655274958,10.48768194,11.29686263,12.07695119,12.82327815,13.53255969\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.140199092,7.934783212,8.720670981,9.492461139,10.24558533,10.97610672,11.68073483\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.382030056,8.187525452,8.981919076,9.760170964,10.51803648,11.25186635,11.95862286\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.936182486,9.794943289,10.63422551,11.44761111,12.22960313,12.97598564,13.68391919\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.969542514,10.73703521,11.47996807,12.19499825,12.87942333,13.53123514,14.14916306\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.905215446,10.66636193,11.40435816,12.11571386,12.79758218,13.44781016,14.06498469\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.814544331,9.661326288,10.49222324,11.30047223,12.08004687,12.8261605,13.53544297\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.355944846,8.15477904,8.943653603,9.717521809,10.47205962,11.2035052,11.90869662\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.313527003,8.113991851,8.905100522,9.681177368,10.43757848,11.17040192,11.87644898\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.923002357,9.78169073,10.62107012,11.43477948,12.21732462,12.96446387,13.67331982\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.946313065,10.71630386,11.46173144,12.179201,12.86596866,13.51999919,14.14000715\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,9.919371289,10.6834429,11.42398142,12.13753866,12.8212963,13.47312739,14.09164534\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,8.897744642,9.740954609,10.56898419,11.37490583,12.15256798,12.89709194,13.60504012\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.327679023,8.130137286,8.921667752,9.697526116,10.45360884,11.18630972,11.89257304\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,7.429782605,8.225105414,9.010528213,9.781084202,10.53248816,11.26099014,11.96342491\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.43101253,19.12274985,19.71739207,20.22900082,20.67015485,21.05173935,21.38299568\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.03873055,18.73298182,19.32967385,19.84297864,20.28555109,20.6683319,21.0006044\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.24674944,18.93922823,19.53453244,20.04673517,20.48842154,20.87048171,21.2021619\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.41127082,19.10230652,19.6967037,20.20833853,20.64967582,21.03153015,21.36309903\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.43072939,19.12249147,19.7171542,20.22878003,20.66994836,21.05154491,21.38281145\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.04475049,18.73899762,19.33568763,19.84899178,20.29156451,20.67434614,21.00661982\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.24426734,18.93666464,19.53190657,20.04406066,20.48570834,20.86773726,21.19939185\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,18.41141029,19.10243567,19.69682524,20.20845432,20.64978721,21.03163809,21.36320425\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.45458344,15.30635988,16.06169148,16.73608913,17.34151148,17.88735081,18.38114463\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.6766986,15.48613896,16.20514472,16.84855431,17.42770624,17.95141686,18.42668786\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.57970846,15.40549074,16.1423188,16.80322843,17.39859235,17.93676688,18.42459893\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,16.07744454,16.72761387,17.31181527,17.8404627,18.32130275,18.76026327,19.16202853\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.51730414,15.35645946,16.1016926,16.76791623,17.36664965,17.90695951,18.3961393\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.77849201,15.43854212,16.03519959,16.57725651,17.07155302,17.5235233,17.93759832\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.38396993,15.23494585,15.9910258,16.66697063,17.27434175,17.82231745,18.31831651\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.36201971,16.09743842,16.75359599,17.3433013,17.87624119,18.3599059,18.80023792\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.85930447,15.66144332,16.37454266,17.01296981,17.58765758,18.1071229,18.57817451\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.06978555,15.83296679,16.51272977,17.12276349,17.67340879,18.17264804,18.62679815\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.40285354,15.24321045,15.9914912,16.66152496,17.26428898,17.80858605,18.30158674\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.75023285,16.35554838,16.90443084,17.40483757,17.862791,18.28297918,18.66917729\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.50381436,15.35220242,16.10488687,16.77712666,17.38070555,17.92489938,18.41717148\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.86081231,15.64856746,16.34847627,16.97519324,17.53982141,18.05093091,18.51528589\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.1885747,15.95081467,16.63039503,17.24043336,17.79092032,18.28964108,18.74282315\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.81649856,15.61965952,16.33201682,16.96877005,17.54143119,18.05889495,18.52819523\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.45501277,15.30674087,16.06203227,16.73639635,17.34179049,17.88760595,18.38137942\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.67609727,15.4856283,16.20470784,16.84817807,17.42738035,17.95113318,18.4264399\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.57867227,15.40458019,16.14151429,16.80251392,17.39795463,17.93619504,18.42408391\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,16.07671261,16.72697013,17.31124444,17.83995277,18.32084415,18.75984826,19.16165078\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.51693971,15.35619337,16.10150821,16.76780009,17.36659087,17.90694921,18.39617017\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.80108805,15.4612498,16.05799127,16.60011299,17.0944606,17.54647199,17.96058066\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.38381108,15.23483873,15.99095916,16.66693619,17.27433326,17.82233012,18.31834656\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.36125328,16.09675691,16.75298501,17.34274963,17.87573991,18.35944785,18.79981724\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.8595464,15.66164502,16.37470989,17.0131075,17.58776981,18.10721308,18.57824542\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.06988407,15.83304459,16.51278986,17.12280843,17.6734408,18.17266905,18.62680981\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.40137588,15.24174181,15.99003061,16.66007147,17.26284178,17.80714444,18.30015013\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.73850642,16.34354619,16.89221334,17.39244857,17.85026306,18.27033704,18.65644014\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.5048183,15.35307229,16.10565139,16.77780687,17.38131696,17.92545356,18.4176772\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.8625918,15.65012258,16.3498468,16.97641028,17.54090947,18.05190949,18.51617065\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,15.18795676,15.95026858,16.62990673,17.23999231,17.79051833,18.28927163,18.74248095\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [In], topology dia,\",,,14.8160792,15.61929925,16.33170838,16.96850681,17.54120729,18.05870533,18.52803556\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,18.39208217,18.6911134,18.92776226,19.11790382,19.27276427,19.40043196,19.50683661\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,13.87151962,14.12432966,14.32466356,14.48580911,14.61718288,14.72558152,14.81599545\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.692958874,4.397952636,5.118963512,5.837174178,6.53863664,7.213930568,7.857403433\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.465771719,4.136896987,4.830677238,5.528214945,6.21512599,6.881337552,7.52044934\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.28053181,3.876154371,4.4980894,5.131873182,5.765394718,6.389282428,6.996818056\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.403720897,4.084101395,4.789198222,5.499213071,6.198864177,6.877372767,7.527866043\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.393505234,4.061072601,4.753847902,5.45244986,6.141997524,6.811996763,7.455724835\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.060564127,3.636244858,4.242237772,4.864142304,5.489691786,6.109209335,6.715585246\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.745928245,4.454129921,5.176471604,5.89456373,6.594816609,7.268086739,7.908924755\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.671726011,4.35958662,5.061557703,5.760376359,6.443273657,7.101575064,7.730006041\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.338268173,3.954047652,4.590367733,5.233147437,5.870859595,6.494773167,7.098791309\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.649950456,4.352431263,5.071388103,5.788011181,6.488324869,7.162860286,7.805907142\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.578911282,4.259309874,4.959045606,5.659671852,6.347324576,7.012419876,7.648974796\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.19885279,3.785697809,4.400713096,5.029522253,5.659914591,6.282320639,6.88978654\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.352593534,4.030484151,4.733808,5.442791543,6.142129373,6.820995278,7.472459959\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.372756009,4.036795043,4.726535587,5.42269392,6.110405669,6.779140691,7.422111596\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.068686017,3.643484972,4.248277546,4.868817078,5.492958298,6.111109615,6.716214888\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.53516487,4.22212451,4.929687087,5.638854881,6.335163923,7.008554598,7.652735274\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.581110784,4.262812246,4.961263302,5.658786786,6.342178292,7.002370918,7.633763659\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,3.147337967,3.748911246,4.37595336,5.013847794,5.650421515,6.276308407,6.884842926\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,6.577411794,7.350562608,8.11974688,8.879295117,9.624458178,10.35108305,11.05558435\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.170852234,7.958516112,8.742664004,9.517070257,10.27589648,11.01394039,11.72686492\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.317806877,10.08758191,10.83940096,11.56713041,12.26610066,12.93309516,13.56618116\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.862506518,8.607516326,9.343848249,10.06874315,10.77861444,11.46968137,12.13845343\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.570906414,10.28840316,10.98915553,11.66912799,12.32480389,12.95344218,13.55313791\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.051282514,9.792879846,10.51656937,11.21847841,11.89533809,12.54455543,13.16425981\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,6.85172322,7.652311727,8.447123218,9.227822469,9.988298494,10.72407152,11.43192274\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.096996494,7.88898403,8.677025025,9.454844398,10.21660269,10.95712571,11.67212007\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.205494883,9.962883594,10.70282726,11.4200769,12.1103895,12.77066811,13.39891298\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.831863981,8.583536823,9.326438597,10.05734504,10.77241181,11.46774424,12.13983513\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.555185453,10.28087828,10.98928255,11.67613857,12.3378073,12.97149899,13.57531607\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.065885441,9.814392697,10.54638923,11.25701332,11.94224871,12.59899764,13.22509687\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,6.596613755,7.362459176,8.128058204,8.88687882,9.633342676,10.36258564,11.0704583\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.163965719,7.957774152,8.748234894,9.528742262,10.29319559,11.03623687,11.75345842\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.244587592,10.02033722,10.77830832,11.5121715,12.21711125,12.88980808,13.52826248\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.810025061,8.557933368,9.298249933,10.02752847,10.74175637,11.43690344,12.10934722\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,8.876915292,9.602389441,10.3122566,11.00145741,11.66582192,12.30222406,12.90856452\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.845471525,8.593142149,9.326118223,10.03875258,10.72650312,11.3859282,12.01464473\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,6.46548722,7.236979509,8.0028529,8.757786722,9.497469617,10.21816972,10.91665409\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.132449778,7.925682523,8.715825378,9.496243369,10.26079265,11.00406878,11.72162103\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.17391141,9.941886696,10.69200742,11.41821594,12.11589213,12.78184266,13.41413692\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.812074692,8.559335682,9.297352873,10.02339297,10.73394535,11.42532264,12.09412588\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.587779833,10.31086439,11.01684623,11.70152838,12.36132341,12.99347708,13.59610677\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.059331446,9.802798572,10.52832637,11.23208556,11.91079436,12.56182466,13.18326882\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,6.793888735,7.598593834,8.398448264,9.184664915,9.950769433,10.69200626,11.40496189\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.080756968,7.880189864,8.676496297,9.462786817,10.23273716,10.98083587,11.70258671\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.184058726,9.951330896,10.69975279,11.42418454,12.12048711,12.78567041,13.41784628\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.833883272,8.589948523,9.336785126,10.07118193,10.78930067,11.48725534,12.161555\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.566074804,10.29069119,10.99810224,11.68408096,12.34501722,12.97813985,13.58155829\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.106810849,9.852449664,10.58059972,11.28689542,11.96770751,12.62021064,13.2424138\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,6.667601442,7.431358781,8.190697603,8.940360312,9.675947076,10.39358024,11.08986902\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.147235674,7.942697405,8.734926888,9.517211768,10.28336895,11.02798312,11.74661206\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,9.24133123,10.00869576,10.75836114,11.48446476,12.18244477,12.84909314,13.48243084\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.800157095,8.545571634,9.282990729,10.00927595,10.72059643,11.41302406,12.08298821\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,8.869168776,9.59552949,10.30666092,10.99735101,11.66328841,12.30123692,12.90902221\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,7.937201026,8.68224972,9.41197344,10.12120126,10.80567867,11.46212439,12.08823359\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,11.09438426,11.85504673,12.58242665,13.27591753,13.9347437,14.55832486,15.14646637\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,10.88577861,11.67361506,12.42799808,13.14716649,13.82955596,14.47413734,15.08053988\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,10.33377071,11.10019419,11.83426362,12.53466778,13.20012515,13.82972897,14.42310371\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,11.12143031,11.8834711,12.61240612,13.3074505,13.96770603,14.59251945,15.18166139\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,10.93699698,11.7239289,12.47690836,13.19441643,13.8750606,14.51792523,15.12270869\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,10.41195165,11.17768575,11.9108846,12.61033884,13.27483742,13.90351884,14.49603392\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,15.46695904,16.15308284,16.76836697,17.32369989,17.82738807,18.28592429,18.70451617\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,15.27032411,15.95063991,16.56363657,17.11792476,17.62078615,18.07830716,18.49558115\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,14.96961971,15.77395594,16.49797905,17.14948081,17.73567074,18.26319909,18.73816732\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,16.03936596,16.58214433,17.07077862,17.51346034,17.91703878,18.28707389,18.62800083\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,15.59937626,16.22821232,16.79773703,17.31590602,17.78889896,18.22166026,18.61826692\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,14.94921667,15.6520795,16.28264779,16.85089245,17.36502635,17.83178777,18.25673652\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,15.62558835,16.26485349,16.84106724,17.36355628,17.83945956,18.27437023,18.67278577\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,14.58658684,15.22838308,15.80931393,16.33674798,16.81706113,17.25563997,17.65701299\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,15.03280669,15.85024173,16.58475683,17.24444343,17.836858,18.36899265,18.84725897\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,16.11684162,16.6508035,17.13262802,17.56997679,17.96931759,18.33592613,18.6740226\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,15.52538863,16.18880976,16.7863111,17.32754525,17.81995673,18.26941343,18.68065676\n\"linker [O-]C(=O)c1ccnc(c1)c1nccc(c1)C(=O)[O-], nodes [Ce], topology rna,acs\",,,15.17310065,15.89091567,16.53184803,17.10748453,17.6271455,18.09831714,18.52705212\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,20.29504329,20.75936887,21.12463525,21.41659468,21.65331646,21.84771997,22.009209\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,20.29368865,20.75821944,21.12364974,21.41574161,21.65257163,21.84706456,22.00862817\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,20.29522468,20.75952317,21.12476784,21.41670967,21.65341703,21.84780862,22.00928767\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,20.29398839,20.75847373,21.12386758,21.41592995,21.65273583,21.84720881,22.0087558\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.27608958,3.895780962,4.542966003,5.201186348,5.857040533,6.500454733,7.124439141\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.336011998,3.962528566,4.616402128,5.280669051,5.941560438,6.588783075,7.215254535\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.521898098,4.147243653,4.797900864,5.457200135,6.111846202,6.752040726,7.371139311\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.276033304,3.895734245,4.542929227,5.201159467,5.857023223,6.50044654,7.124439606\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.336075184,3.962604457,4.616489235,5.280765586,5.941664501,6.5888928,7.21536819\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.52200147,4.14734636,4.797999794,5.457293232,6.111932294,6.752119321,7.371210398\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.275977996,3.895670669,4.542858701,5.20108352,5.856943479,6.500364648,7.124357183\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.336048004,3.962562519,4.616434133,5.280699221,5.941588881,6.588809888,7.21527981\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.521994599,4.147342119,4.797998511,5.457294961,6.111936918,6.752126638,7.371220179\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.275967007,3.895651653,4.542832711,5.201051626,5.856906673,6.500323777,7.124312918\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.336037671,3.962556112,4.616429602,5.280695177,5.941584471,6.588804652,7.215273555\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,3.522024036,4.14738139,4.798046682,5.457350769,6.111998958,6.7521935,7.371290535\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,6.619764269,7.438123466,8.243057944,9.029806385,9.794726978,10.53486086,11.24779507\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.326984443,10.0641211,10.78646736,11.4893585,12.16858295,12.82074395,13.44338767\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,7.593802169,8.330491519,9.064613694,9.792955585,10.5108847,11.21341834,11.89593995\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.082861201,9.821564615,10.54978423,11.2613124,11.95074666,12.61384558,13.24759198\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.482731247,10.18019147,10.8716822,11.5511306,12.21283576,12.85206175,13.46524522\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,6.619990171,7.438294393,8.243183553,9.029894984,9.794785676,10.53489567,11.24781101\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.326790044,10.06394506,10.7863068,11.48921106,12.16844677,12.82061752,13.4432698\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,7.593647278,8.330341844,9.064468632,9.792814753,10.5107479,11.21328551,11.8958111\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.082554936,9.821278817,10.54951914,11.2610676,11.95052133,12.61363858,13.24740205\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.482672816,10.18012904,10.87161408,11.5510561,12.21275495,12.85197519,13.46515376\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,6.619780612,7.438132211,8.24306435,9.02981389,9.794737693,10.53487594,11.247815\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.326865482,10.06401562,10.78637139,11.48926929,12.16849871,12.82066353,13.44331039\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,7.593704375,8.330407607,9.064543571,9.792898796,10.51084048,11.21338568,11.89591772\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.08280343,9.821514125,10.54974187,11.2612784,11.95072085,12.61382745,13.24758087\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.482686739,10.18014714,10.87163773,11.55108584,12.2127907,12.85201649,13.46519994\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,6.61989652,7.438234584,8.243149632,9.029880817,9.794786483,10.53490771,11.24783135\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.326929672,10.06406993,10.78641835,11.48931079,12.16853608,12.82069772,13.44334205\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,7.593778717,8.330465551,9.064586788,9.792928906,10.51085906,11.21339426,11.89591773\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.082567157,9.821295063,10.54953825,11.2610887,11.9505437,12.61366168,13.24742542\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.482658249,10.18012644,10.87162494,11.55108061,12.2127924,12.8520243,13.465213\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.735241308,10.58337318,11.39230637,12.16255019,12.89392973,13.58614185,14.23910441\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,10.11238492,10.91930992,11.68811698,12.4205782,13.11731697,13.77841307,14.4038549\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.735088755,10.58323994,11.39219067,12.16245007,12.89384327,13.58606726,14.23904007\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,10.1123377,10.91928547,11.68811195,12.42058918,13.11734078,13.77844686,14.40389627\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.735171859,10.58331503,11.39225616,12.16250547,12.89388883,13.58610364,14.23906815\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,10.11237656,10.91931307,11.68813049,12.42060082,13.11734738,13.77844993,14.40389695\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,9.735172891,10.58331285,11.39225229,12.16250084,12.89388395,13.5860988,14.23906351\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,10.11238721,10.91931172,11.68811954,12.42058224,13.11732282,13.77842077,14.40386433\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,22.23626915,22.49666001,22.70197253,22.86651358,23.0002968,23.11047456,23.20225289\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,22.23628264,22.49667279,22.70198457,22.86652489,23.00030742,23.11048453,23.20226227\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,22.23639468,22.49676692,22.70206444,22.86659329,23.00036648,23.11053592,23.20230729\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,22.23616835,22.4965758,22.70190148,22.86645306,23.0002448,23.11042951,23.20221356\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,12.94652739,13.78266693,14.5442631,15.24070287,15.8791368,16.46527259,17.00387613\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,13.37465865,14.216684,14.97139433,15.65192768,16.26865111,16.82980833,17.34204221\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,12.94921115,13.78510747,14.54648952,15.2427397,15.88100492,16.46698997,17.00545837\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,13.37819301,14.21992077,14.97437139,15.6546764,16.27119753,16.83217417,17.34424584\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,12.94663226,13.78268837,14.54422717,15.24062824,15.87903679,16.46515669,17.00375106\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,13.37797958,14.21966912,14.97408798,15.65436793,16.27087031,16.83183391,17.34389747\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,12.9451154,13.78142197,14.54315792,15.23971516,15.87824839,16.46446871,17.00314474\n\"linker [O-]C(=O)c1cnccn1, nodes Cl[Ni], topology \",,,13.37688356,14.21876977,14.97335239,15.65376879,16.27038486,16.83144317,17.34358556\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,17.11676121,17.73628905,18.25796506,18.70162562,19.08218887,19.41107761,19.6971845\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,17.01838177,17.64845381,18.17912187,18.6305384,19.01784597,19.35263497,19.64392851\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,3.310634798,3.971200136,4.652764901,5.33880721,6.016330679,6.675921309,7.311355774\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,3.325517824,3.983198426,4.66207305,5.345649213,6.020939674,6.678520629,7.312144942\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,3.326202375,3.983875835,4.662698765,5.346203517,6.021429299,6.6789767,7.312619048\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,3.301727005,3.961900318,4.643428585,5.329703015,6.007640586,6.667754296,7.303765193\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.549958248,8.345413374,9.129484774,9.898432025,10.64799816,11.37406073,12.07307329\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.138222421,8.009697005,8.864818056,9.697627053,10.50306813,11.27705478,12.0165356\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,9.162761429,10.00031889,10.80046735,11.56160849,12.28290417,12.96414581,13.60566829\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,6.55372919,7.308102342,8.059541581,8.803632745,9.536081908,10.25272834,10.94973759\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.060525493,7.952520516,8.826095149,9.672298967,10.48530664,11.26152677,11.99897198\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.506727879,8.312520416,9.105801226,9.882628193,10.63875778,11.37018338,12.0735129\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.205444672,8.071774325,8.921779049,9.74964173,10.5503993,11.32001984,12.05547811\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,9.245540234,10.06843613,10.85529853,11.60471712,12.31586436,12.98844483,13.62265813\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,6.677761855,7.444149282,8.206892236,8.960590892,9.700547572,10.42254393,11.12287982\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.000602393,7.869622389,8.723725865,9.553728411,10.35347672,11.11905101,11.84816144\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.506252511,8.31159615,9.104526942,9.881107182,10.63708266,11.36843024,12.07174041\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.201784098,8.067454767,8.916574652,9.743501544,10.54337831,11.31223047,12.0470578\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,9.235436121,10.05935903,10.84726927,11.59770706,12.30981407,12.98327829,13.61829273\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,6.666029737,7.436717783,8.203067163,8.959732473,9.702088239,10.4259932,11.12782197\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,6.972943557,7.839139045,8.691567173,9.520749161,10.32031503,11.0861787,11.81592039\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.54489034,8.34133933,9.126405287,9.896283799,10.64668335,11.37346763,12.07308947\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.138062571,8.010195277,8.865852279,9.699082783,10.50484024,11.27905063,12.01867688\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,9.161172908,9.999263225,10.79995084,11.56160724,12.28337612,12.96503887,13.60692612\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,6.55542538,7.308828688,8.059582392,8.803204607,9.535348827,10.25181264,10.94872859\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,7.070189185,7.963040278,8.836502508,9.681754367,10.49315776,11.26732357,12.00245257\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,13.61425695,14.44996073,15.20354362,15.8857907,16.50515165,17.06851626,17.58169256\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,13.54008863,14.39728117,15.16744509,15.86244961,16.49159613,17.06243743,17.58129658\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,14.11859233,15.06022016,15.90307729,16.65602805,17.3279598,17.92744498,18.46251551\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,15.84580193,16.46493783,17.00656397,17.48679318,17.91767162,18.30815894,18.66490916\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,14.20485859,14.923657,15.57921359,16.17987442,16.73174677,17.23957283,17.70724992\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,14.36464185,15.06957995,15.71430602,16.30649725,16.85163744,17.35395526,17.81695661\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,13.02130285,14.03848751,14.9597254,15.78955045,16.53432865,17.20135727,17.79819212\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,15.90450143,16.51040784,17.04093885,17.51201206,17.93532887,18.31952326,18.67099044\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,13.83378413,14.58345846,15.267117,15.89319869,16.46800049,16.99648895,17.48278915\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,14.65785416,15.34041483,15.96425685,16.53717185,17.06463745,17.55081475,17.99911189\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,13.67324358,14.62302151,15.48608036,16.26531376,16.96584309,17.59399123,18.1565297\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,15.76849093,16.38459697,16.92516395,17.40567476,17.83766109,18.22972262,18.58828585\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,13.76802593,14.59082404,15.33286495,16.00479245,16.61491055,17.16997538,17.67567783\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,13.61886466,14.46504048,15.22603591,15.91340101,16.53616024,17.10163642,17.61596558\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,14.67327293,15.55452942,16.34497001,17.05240923,17.68477533,18.24979031,18.75474736\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Co], topology pcu,\",,,15.53075943,16.18959421,16.7633917,17.26984586,17.72226959,18.13062608,18.50235686\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,20.95392473,21.12200969,21.25279625,21.35649835,21.44007578,21.50839753,21.5649496\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,20.99287919,21.15303063,21.2781789,21.37772451,21.4581406,21.52399353,21.57857424\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,20.95389466,21.12198294,21.25277248,21.3564772,21.44005692,21.50838064,21.56493441\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,20.99292817,21.15307222,21.27821464,21.37775553,21.45816777,21.52401751,21.57859554\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.380445217,4.004572031,4.652376622,5.308643388,5.96092814,6.599862872,7.218963552\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,3.380374126,4.004492783,4.652292149,5.308555966,5.960839498,6.5997743,7.218875997\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.00122959,7.790891654,8.570596771,9.335073119,10.08017091,10.80250525,11.49933067\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.350624838,8.161524365,8.966000672,9.757988854,10.5315507,11.281416,12.00330078\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.139855233,8.005190713,8.856192772,9.686204707,10.48987446,11.26300799,12.0025104\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,6.828124717,7.603399912,8.37269254,9.130869546,9.873505589,10.59669218,11.29705444\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.453760464,10.25597641,11.02462021,11.75880881,12.45769692,13.1207145,13.74769192\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.274667987,8.12745135,8.967002338,9.787120986,10.58247421,11.348688,12.08242351\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,6.763742243,7.569365727,8.366142568,9.147803057,9.90951527,10.64746907,11.35868997\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.319707361,8.138586271,8.949834662,9.747461694,10.5256494,11.2792624,12.00414911\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,6.972256465,7.759596636,8.53803102,9.302059524,10.04738405,10.77048901,11.46850283\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.001432419,7.791084794,8.570776591,9.335237243,10.08031803,10.80263496,11.49944319\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.350668123,8.161547185,8.966001418,9.757966969,10.53150666,11.28135111,12.00321692\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.139996555,8.005311132,8.856288225,9.686273352,10.48991618,11.26302395,12.00250255\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,6.82803698,7.603334311,8.372643426,9.130832735,9.873478008,10.59667158,11.29703916\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.453962607,10.25614805,11.02476243,11.75892325,12.4577857,13.12077998,13.74773664\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.274736461,8.127511475,8.967050703,9.787155883,10.58249516,11.34869533,12.08241813\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,6.763606383,7.569253454,8.36604793,9.147721164,9.90944227,10.64740204,11.35862678\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,7.319669745,8.138549886,8.949796767,9.747420307,10.5256033,11.279211,12.00409234\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,6.972305294,7.75965476,8.538095596,9.302128476,10.04745581,10.77056236,11.46857683\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.554343491,10.46138951,11.32322665,12.13793841,12.90508806,13.62515794,14.29924632\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,9.554434552,10.46146709,11.32328935,12.13798588,12.90512074,13.6251768,14.29925266\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.60264576,16.2845158,16.89582094,17.44722288,17.94701638,18.40175308,18.81670867\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.69912845,16.39075092,17.00481929,17.55491626,18.05109394,18.50097377,18.91048693\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.77776793,16.44241685,17.03056226,17.55682123,18.03177152,18.46323779,18.85714484\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.1621702,15.89949939,16.56270324,17.16192246,17.70508848,18.1986158,18.64784876\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.0314776,15.82641829,16.53618898,17.1729052,17.74604341,18.26327174,18.73098038\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.92113588,16.55902041,17.12481034,17.63136179,18.08851274,18.50382396,18.88314792\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.19790282,15.92812323,16.58332095,17.17375481,17.70780893,18.19237294,18.63316751\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.57871079,16.24908143,16.85271562,17.39905345,17.89560319,18.34839936,18.76236745\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.60200442,16.28394321,16.89531015,17.44676666,17.94660791,18.40138619,18.81637794\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.69864382,16.39034585,17.00447402,17.5546169,18.05083054,18.50073903,18.91027545\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.77415788,16.43927296,17.02780886,17.55439658,18.02962521,18.46132846,18.85543841\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.1634288,15.90061113,16.5636836,17.16278662,17.70585064,18.19928889,18.64844429\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.0280171,15.82337652,16.53350355,17.17052333,17.74392089,18.26137165,18.72927187\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.92163254,16.55943062,17.12514992,17.63164307,18.08874551,18.50401614,18.88330599\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.19695447,15.92735289,16.58268948,17.17323328,17.70737549,18.19201078,18.6328635\n\"linker [O-]C(=O)c1nc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Cd], topology \",,,15.57922566,16.24950915,16.85307264,17.3993526,17.89585464,18.34861126,18.76254643\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,19.00784081,19.61440711,20.10035542,20.4945447,20.81804546,21.08640537,21.31123308\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,18.99879713,19.60626808,20.09305871,20.48800672,20.81217953,21.08112985,21.30647452\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,19.00798207,19.61453115,20.10046475,20.4946415,20.81813156,21.08648232,21.31130218\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,18.99896862,19.60641727,20.09318923,20.48812157,20.81228115,21.08122028,21.30655541\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.764212927,5.159371271,5.599794303,6.073593232,6.568829589,7.074917789,7.583237461\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.765221297,5.160177921,5.600427182,6.074075755,6.569182435,7.075159582,7.583384967\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.783234482,5.173671811,5.610479535,6.081480661,6.574520624,7.078849881,7.585723064\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.780523588,5.171194025,5.608202661,6.079386554,6.572602195,7.077109277,7.584170112\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.763411949,5.15860076,5.599047011,6.072865245,6.568119426,7.074225657,7.582564648\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.766515324,5.161475352,5.601732094,6.075387399,6.570496358,7.076468812,7.584681082\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.783091486,5.173527639,5.610335625,6.081338944,6.574383677,7.078720978,7.585606118\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.780054902,5.170723813,5.607730803,6.078915638,6.572137371,7.076657947,7.583741485\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.870360977,5.231936017,5.637458905,6.077269488,6.540965607,7.018876559,7.502804911\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.876356822,5.235636258,5.639149659,6.077210687,6.53940129,7.016036612,7.498903219\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.87043748,5.23200268,5.637517278,6.077320756,6.541010726,7.018916329,7.502840014\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,4.876371031,5.235647936,5.639159417,6.077218959,6.539408385,7.016042749,7.498908551\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.00838956,10.49299402,10.99491049,11.51078777,12.03516196,12.56190878,13.08514651\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.00882391,10.4933277,10.9951736,11.51099985,12.03533594,12.56205346,13.08526801\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.04940961,10.52238129,11.01515521,11.52388434,12.04270481,12.56516684,13.08512392\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.05194721,10.52452353,11.01696395,11.52541205,12.04399627,12.56626051,13.08605302\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.00856742,10.4931884,10.99510879,11.51098143,12.0353455,12.56207902,13.0853019\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.00820536,10.49272151,10.99459437,11.51045701,12.03483474,12.56159593,13.08485388\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.04956299,10.52252257,11.01528442,11.52400171,12.04281087,12.56526238,13.08520997\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,10.0521595,10.52473807,11.01717522,11.52561651,12.04419196,12.56644665,13.08622972\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,9.775458574,10.25957086,10.76165437,11.2784324,11.80443185,12.33349301,12.85968869\n\"linker [O-]C=O, nodes [Fe], topology pcu\",,,9.776681041,10.2582858,10.75875666,11.27452971,11.79993679,12.32868488,12.85475523\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,18.41424714,18.59107403,18.73014265,18.84124188,18.93125465,19.00511078,19.06640329\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,19.06864208,19.2160201,19.33203199,19.42483802,19.50014554,19.56203237,19.61346837\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,20.0603642,20.23698929,20.37600735,20.48713637,20.57721987,20.65116571,20.71255471\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,20.12993574,20.27925888,20.39677016,20.49075367,20.56700123,20.62964957,20.68171053\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.54273095,4.077372412,4.627841522,5.185625787,5.74322812,6.29447858,6.834621867\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,4.47987427,5.093013261,5.697902411,6.289118655,6.862360894,7.414349931,7.94274317\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,2.630726525,3.056973575,3.524300459,4.022960331,4.542676965,5.073845914,5.608232178\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,2.55011086,2.975435465,3.443727031,3.944650018,4.467650617,5.003053766,5.542665573\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,2.271465206,2.68070398,3.134070526,3.621904308,4.134016069,4.660842632,5.194123797\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,2.40845907,2.834844032,3.302483032,3.801414454,4.321222389,4.852219397,5.386128938\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,4.065996102,4.673707481,5.28011989,5.877827042,6.461016038,7.025270908,7.567399851\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.193787563,3.712209809,4.252062515,4.804268863,5.360689473,5.914508058,6.46036687\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.777462103,4.316770567,4.869216112,5.42661839,5.981867255,6.529182651,7.064166942\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,4.735868861,5.34852166,5.950207364,6.536247063,7.102942787,7.647494131,8.167929257\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.473725675,3.911424697,4.389247427,4.897099166,5.42454719,5.961973772,6.50122511\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.267779852,3.685148519,4.145917353,4.64041052,5.158529721,5.690862742,6.229319342\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.394855233,3.811157115,4.271135695,4.764750105,5.281567204,5.811912177,6.347517061\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.574148017,4.005633416,4.477894513,4.980758087,5.503674615,6.036902653,6.572174634\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.655611536,4.232030503,4.817131571,5.402534135,5.981366001,6.548267643,7.099321598\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,3.238262252,3.7714493,4.324959335,4.889207069,5.455874302,6.018161251,6.570832437\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,16.45023013,16.97906517,17.40689584,17.76150413,18.06321713,18.32684181,18.56307267\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,17.02273014,17.47894996,17.84443343,18.1451737,18.39988917,18.62209584,18.82150974\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,16.8312893,17.29829805,17.67380155,17.98331388,18.24541111,18.47363807,18.67782399\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,17.66421289,18.00549625,18.27844705,18.50294546,18.69338026,18.86023779,19.01113752\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,9.52304106,10.11504269,10.72180858,11.33187791,11.93476682,12.52202748,13.08748339\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,8.585621745,9.17733224,9.784679141,10.39579825,10.99995061,11.58853369,12.15528187\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,16.97420335,17.43050107,17.79660567,18.09820883,18.35387321,18.57703601,18.7773751\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,17.20049287,17.62478793,17.96364224,18.24197012,18.47760635,18.68337932,18.8684839\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,16.72603175,17.21659563,17.611933,17.93829205,18.21485615,18.45564424,18.6708442\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,16.88431552,17.36242502,17.74694469,18.06399619,18.33257749,18.5665172,18.77582931\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,10.70020858,11.28962353,11.89370482,12.50113753,13.10153953,13.68652785,14.24996202\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,10.65840982,11.26102823,11.87781659,12.49671924,13.10701572,13.70024248,14.27032811\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,18.12070339,18.53596239,18.86975,19.14517458,19.37884678,19.58271359,19.76532153\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,18.61008115,18.95548997,19.23128543,19.45788027,19.64981992,19.81752534,19.96843839\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,17.94403395,18.3662671,18.70567137,18.98504849,19.22098565,19.42558434,19.60764685\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,15.61967477,15.89352183,16.11399239,16.29629593,16.45160164,16.58813706,16.71192695\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,13.78860887,14.5194409,15.18329699,15.78763986,16.33837954,16.84050963,17.29845445\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,13.5550111,14.2826748,14.94415324,15.54692977,16.09686349,16.59886009,17.05724248\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,18.60171286,18.93841794,19.20781021,19.42956287,19.61774836,19.7824764,19.93097872\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,18.73529292,19.05730078,19.31399532,19.52477032,19.7034127,19.85978785,20.00093384\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,17.86284711,18.2806677,18.61730898,18.89507311,19.13022976,19.33466206,19.5170104\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,17.96430883,18.3883689,18.72965201,19.01092487,19.24877462,19.45530308,19.63930331\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,13.91026199,14.65174715,15.32467914,15.93676863,16.4941511,17.00200964,17.46492287\n\"linker NCCN, [C]#N, nodes [Cd], topology cdq\",,,13.99798003,14.71524489,15.36767965,15.96291639,16.50676042,17.00398372,17.45875954\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,14.41559189,15.47364762,16.3738923,17.14109523,17.79690384,18.3596736,18.8447126\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,14.3990041,15.46046217,16.36387898,17.13395634,17.79232903,18.35736684,18.84440402\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.268017758,3.920907484,4.598568189,5.283323475,5.961187513,6.621981683,7.25893374\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.285690328,3.93781592,4.614566332,5.298360842,5.97528155,6.635198015,7.271371874\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,2.629051992,3.064116698,3.500124246,3.925849755,4.333522655,4.718350409,5.077846377\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.064313937,3.501075252,3.938413865,4.365364734,4.77427244,5.160381856,5.521205668\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.253771686,3.90490099,4.581248608,5.265136192,5.942526807,6.603170239,7.24021983\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.315014072,3.97140004,4.651304454,5.33718553,6.015231127,6.675441808,7.31121183\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.33711978,3.993781889,4.673692101,5.359358393,6.037025189,6.696745587,7.331957584\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.259022114,3.909422314,4.585149339,5.268518347,5.94548671,6.605797837,7.242597542\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.260619896,3.90951034,4.583973871,5.26636452,5.942638779,6.60252065,7.239130244\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,3.224978326,3.872620303,4.546433159,5.228678306,5.905211169,6.565657601,7.203049162\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.054371011,9.825950753,10.5707914,11.28613037,11.96990433,12.62071917,13.23781874\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.039623432,9.809729582,10.55335831,11.2677449,11.95080926,12.60113454,13.21793971\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.048814374,9.820715452,10.56564631,11.28095976,11.96466304,12.61540212,13.23244145\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.031782884,9.801499817,10.54495934,11.25931333,11.9424288,12.59285376,13.20978296\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.076503984,9.846013515,10.58941032,11.30376015,11.98688454,12.63731038,13.25422484\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.093375748,9.862864214,10.60568442,11.3191478,12.00123436,12.65056984,13.2664011\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.089097414,9.858552625,10.60158374,11.3154666,11.99813619,12.6481741,13.26478862\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,9.096691688,9.866630807,10.60974824,11.32344677,12.00575923,12.65533833,13.27144202\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,7.506032835,8.233390419,8.957756144,9.675687836,10.38256634,11.07355221,11.74422573\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,7.530151225,8.258557254,8.984336517,9.703821884,10.41223628,11.10463841,11.7765502\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,6.000975436,6.775898107,7.548569116,8.312722547,9.063216166,9.795655327,10.50630695\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,7.535690582,8.263328414,8.988090235,9.706452477,10.41373735,11.10506853,11.77600685\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,7.518148983,8.247366298,8.973595287,9.693316487,10.40185008,11.09431636,11.76627442\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,6.002755196,6.775290802,7.544298069,8.303914547,9.049396896,9.776689604,10.48231867\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,5.956015048,6.730002611,7.500749198,8.262216334,9.009552462,9.738638936,10.4459676\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,6.016295247,6.78952984,7.560640617,8.323329282,9.072449797,9.803613363,10.51309334\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.4232829,14.27484237,15.03710248,15.7215694,16.33807442,16.89495353,17.39927161\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.05943375,13.90316447,14.66291594,15.34807055,15.96717352,16.5277829,17.03648874\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.60388895,14.42798139,15.16727324,15.83251021,16.43289901,16.97626056,17.46923266\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.46973309,14.29869276,15.04340044,15.71390949,16.31911269,16.86672005,17.36336209\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.368238,14.21670393,14.97771226,15.66197575,16.27888625,16.83653813,17.34186161\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.49566786,14.32566609,15.07095551,15.7419839,16.34780957,16.89619408,17.39376583\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.20832221,14.04851657,14.80208647,15.47974516,16.0908623,16.64348997,17.14450147\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,13.65476517,14.47230349,15.2060643,15.86652587,16.46270574,17.00229036,17.49182245\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,14.04265405,15.09525635,16.00232323,16.78458936,17.46062811,18.04655886,18.55611936\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Al], [OH], topology rna\",,,14.28918825,15.31505854,16.19834085,16.959642,17.61728571,18.18710263,18.6825441\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,20.74210832,21.22378537,21.60887263,21.92088494,22.17676415,22.38891854,22.56657551\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,20.64440456,21.14042348,21.53712277,21.85860737,22.12227971,22.34090241,22.52397466\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,20.7431685,21.22475862,21.60975609,21.92168313,22.17748444,22.38956909,22.56716422\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,20.66933384,21.16168771,21.55543919,21.87452623,22.13622758,22.35321361,22.53491405\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,20.73759455,21.21991185,21.60552134,21.91796277,22.17419741,22.38664864,22.56455552\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,20.6340773,21.13159855,21.52950851,21.85197985,22.11646505,22.33576407,22.51940422\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.478292076,4.153242012,4.845849891,5.539328188,6.220869948,6.88147018,7.515388323\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.492401436,4.165664882,4.857928695,5.552060211,6.234893546,6.897130972,7.532825204\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.437074626,4.120902044,4.825326365,5.531873749,6.226468887,6.899261366,7.5440162\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.439463327,4.122220545,4.825534482,5.531044473,6.224730716,6.896762643,7.540904515\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.251329535,3.921796533,4.614849603,5.3125604,6.001026247,6.670315066,7.313958989\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.42822349,4.097296814,4.787486288,5.481268578,6.165060882,6.829188684,7.467393622\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.225256369,3.688491771,4.185662344,4.709411278,5.25108557,5.802236809,6.355487226\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,2.929832443,3.405340268,3.921113859,4.46642918,5.030259686,5.60259027,6.175080122\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.022843322,3.492132366,4.001442094,4.540158147,5.097400176,5.663283522,6.229561098\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.230294256,3.675636141,4.156051563,4.664715784,5.19328175,5.733398685,6.277628958\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,2.031688965,2.48439808,2.995602497,3.551644287,4.138238095,4.742277097,5.352748082\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.082650555,5.491176427,5.922256868,6.371057566,6.831621176,7.298000509,7.764922209\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.339757317,5.731546524,6.14481368,6.576067037,7.020133881,7.471462543,7.924929463\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.251724856,5.652884435,6.077382893,6.520372399,6.975793039,7.437579039,7.900356685\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.034778081,3.503870998,4.012718356,4.55088494,5.107588115,5.672984084,6.238833044\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.206158092,3.650757955,4.129581516,4.636317633,5.162981031,5.701446721,6.244397658\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.477661264,4.152601851,4.845188878,5.538641749,6.220158457,6.880737111,7.514638785\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.48966874,4.16265509,4.854736805,5.548765078,6.23155808,6.893803756,7.529542656\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.436234841,4.120084784,4.824526932,5.531090905,6.225703223,6.898514288,7.543289324\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.439587808,4.122327692,4.825634469,5.531142738,6.224829688,6.896862996,7.541005999\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.249715174,3.920002387,4.612922768,5.310543843,5.998957137,6.668224264,7.311871269\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.429545248,4.098812515,4.789151728,5.483040419,6.166900181,6.831062412,7.469274942\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.225615134,3.689037134,4.186381763,4.710284917,5.2520895,5.80334561,6.356675878\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,2.928804433,3.404352766,3.920159298,4.465504627,5.029364945,5.60172655,6.174249184\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.023409167,3.492663918,4.001945146,4.540637039,5.097857902,5.663722003,6.229981483\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.230563298,3.675796474,4.156105845,4.664671393,5.193149298,5.733190563,6.27735815\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,2.030038808,2.482354625,2.993178033,3.548873231,4.135169099,4.738965708,5.349251028\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.081786512,5.490073202,5.920957635,6.369603336,6.830049484,7.296344602,7.763210722\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.340328723,5.73206147,6.145277268,6.576481317,7.020500136,7.471782301,7.92520481\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.251442146,5.65232641,6.07659839,6.519406168,6.974685198,7.436364765,7.899066203\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.034371135,3.503321653,4.012078245,4.550193228,5.106873406,5.672266548,6.238126391\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.206154812,3.650594587,4.129313039,4.635982593,5.162605937,5.70104942,6.243989842\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.475440263,4.150196634,4.84266979,5.536066667,6.217572964,6.878175821,7.512127096\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.492425094,4.165684066,4.857931664,5.552040501,6.234848666,6.897061141,7.532732317\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.436899763,4.120767975,4.825233999,5.531821063,6.22645211,6.899275895,7.544057228\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.439516602,4.122352565,4.825736099,5.531304878,6.225038749,6.897107681,7.54127698\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.250670043,3.921183419,4.614288872,5.312053912,6.000572965,6.669912102,7.313602411\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.428656247,4.097818042,4.788073253,5.481900148,6.165718966,6.829858633,7.468064067\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.227036719,3.690466895,4.187805157,4.711690052,5.253466754,5.804687372,6.357976313\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,2.928378659,3.403557345,3.919043221,4.464120162,5.027763924,5.5999577,6.172356502\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.024514697,3.493832309,4.003165622,4.541895886,5.099140516,5.665014335,6.231270892\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.231425373,3.676692042,4.157046111,4.665659824,5.19418338,5.734263902,6.278462306\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,2.032678703,2.485667184,2.997150772,3.553451968,4.140272242,4.744497589,5.355112348\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.081190138,5.489593368,5.920566597,6.369279894,6.829777576,7.296112142,7.763008662\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.339903094,5.731735144,6.145038388,6.576320072,7.020407232,7.471748447,7.925220703\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,5.250902205,5.651941492,6.076344741,6.519263208,6.974635074,7.43639216,7.899158194\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.035573972,3.504802887,4.013781042,4.552064882,5.108866919,5.674341358,6.240248449\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,3.205396479,3.650025969,4.128877474,4.635641418,5.162333752,5.700830399,6.24381495\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.857115352,7.645080623,8.428738151,9.202292315,9.960658122,10.69932717,11.41443803\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.339955212,8.176064235,8.99323058,9.78846392,10.55898854,11.30218055,12.01573258\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.893226869,8.687401438,9.465831041,10.2259697,10.96487195,11.67954072,12.36727248\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.886475247,8.681287408,9.459531731,10.21898465,10.9569409,11.67057161,12.35728409\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.551581537,10.33160868,11.08917488,11.81990488,12.52019392,13.18746813,13.82018646\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.479094826,10.25486546,11.00838932,11.73550653,12.43277643,13.09771995,13.72882704\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.460782893,10.23827462,10.99480205,11.72538307,12.42611753,13.09428036,13.72824108\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.841701616,7.622777255,8.400618068,9.169272917,9.923574194,10.65895414,11.37149266\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.90260475,8.694820326,9.471837437,10.23110655,10.96959317,11.68418577,12.37207154\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.454468042,10.23343144,10.99101753,11.72234698,12.42359987,13.09211349,13.72630529\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.427125858,10.22670961,10.99979964,11.74306162,12.45362684,13.12944015,13.76933064\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.834300007,7.618261686,8.398389865,9.168847741,9.924551987,10.6610042,11.37434397\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.849268614,7.635160158,8.417509323,9.190314949,9.948334599,10.68694202,11.40218879\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.459684426,10.23267311,10.98365929,11.70869338,12.40440268,13.06829415,13.69880278\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.24317165,8.086648929,8.913498847,9.719536041,10.50109526,11.25494885,11.97841787\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.897645358,8.688198465,9.462491104,10.21843123,10.95336637,11.66446954,12.34911937\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.577052497,10.32830082,11.06728038,11.78754702,12.48307122,13.14905713,13.78220151\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.682080926,10.45248126,11.20736704,11.93983897,12.64396819,13.31533718,13.95112985\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.650268042,8.465021509,9.283145812,10.09413067,10.88801817,11.65652541,12.393454\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,13.13953915,13.75395572,14.33399185,14.88179063,15.39817329,15.88360553,16.338673\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.397463651,10.18536849,10.96175842,11.71721855,12.44414788,13.13713038,13.79282875\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.856297435,7.644633092,8.428545654,9.202270702,9.960746277,10.6994812,11.41462695\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.342730183,8.178703449,8.99575693,9.790892062,10.56132765,11.30443622,12.01790818\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.892340674,8.686621958,9.4651485,10.22537331,10.96435096,11.67908507,12.36687309\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.888670861,8.683179502,9.461132365,10.22031269,10.95801952,11.67142621,12.35794057\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.550598359,10.33092014,11.08872685,11.81965252,12.52009994,13.18750157,13.82032164\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.482666482,10.25787486,11.01091196,11.73760692,12.43451118,13.09913928,13.72997548\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.458506185,10.23634242,10.99312681,11.72389927,12.42477703,13.0930484,13.72709294\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.845416928,7.626142984,8.403680471,9.172069296,9.926135864,10.66130791,11.37366167\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.903284263,8.695274924,9.472067726,10.2311188,10.96940011,11.68380527,12.37152474\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.455420381,10.23399856,10.99126503,11.72233082,12.42336808,13.09170727,13.7257598\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.430410704,10.22964003,11.00240707,11.74537556,12.45567563,13.13125096,13.77092916\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.83585189,7.619197397,8.398838405,9.168904709,9.9242924,10.66048925,11.37362468\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.847518348,7.633461024,8.415866468,9.188723792,9.946788091,10.6854339,11.40071468\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.458373122,10.23149705,10.98260897,11.70775657,12.40356649,13.06754618,13.69813168\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.242905286,8.08623974,8.912958452,9.718878543,10.50033663,11.2541059,11.97750727\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.89780369,8.688163272,9.462278572,10.21805898,10.95285331,11.66383526,12.34838331\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.573624897,10.32517133,11.06440334,11.78488703,12.48060095,13.14675518,13.78005073\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.681812564,10.45223835,11.20712935,11.93959632,12.6437165,13.31507591,13.95086032\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.644819364,8.459560215,9.277710137,10.088756,10.88273571,11.6513613,12.388429\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,13.14361009,13.75757879,14.33722266,14.88467507,15.40075119,15.88591222,16.34074008\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.398982948,10.18643945,10.9624845,11.71768095,12.44441005,13.13724164,13.79282722\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.857736702,7.645532547,8.429058067,9.202504295,9.9607793,10.69937101,11.41441591\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.340841322,8.176967666,8.994116565,9.789310588,10.55978333,11.30291737,12.0164097\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.893336453,8.687471758,9.465855799,10.22594476,10.96479595,11.67941486,12.36709993\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.88596365,8.680925191,9.459302421,10.21887033,10.95692363,11.67063444,12.35741169\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.550535502,10.33043605,11.08789375,11.818533,12.51874897,13.18596737,13.8186462\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.476544531,10.25253215,11.00624595,11.7335295,12.43094559,13.09601836,13.72724049\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.462167316,10.23966733,10.9961755,11.72671806,12.42740154,13.095506,13.72940467\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.840893621,7.621857376,8.399616337,9.168213117,9.922475279,10.65783136,11.37035833\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.9011139,8.693392056,9.470445531,10.22973333,10.96822826,11.68282446,12.37071312\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.45358619,10.23250723,10.99004723,11.72133313,12.42254878,13.09103336,13.72520496\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.426876506,10.22651538,10.99964725,11.74294061,12.45352923,13.12935993,13.76926334\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.834628858,7.618242904,8.398095692,9.16833218,9.923858234,10.66016829,11.37339657\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,6.846292892,7.6325973,8.415315846,9.188450793,9.946762322,10.68562669,11.40109813\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.459672163,10.23266491,10.98366368,11.70871342,12.40443843,13.06834413,13.69886488\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.243416368,8.086808328,8.913579085,9.719544417,10.50103999,11.25483859,11.97826121\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.898331499,8.688642111,9.46271218,10.21845179,10.95320993,11.66416004,12.34868021\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.57675186,10.32788119,11.06677421,11.78698295,12.48247238,13.14844121,13.78158154\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.681184777,10.45157691,11.20647966,11.93898309,12.64315147,13.31456303,13.95039911\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,7.650992262,8.465797482,9.283972277,10.09500227,10.88892683,11.65746166,12.39440806\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,13.13886043,13.75321438,14.33320509,14.88097363,15.3973391,15.8827651,16.33783523\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.397949022,10.18573679,10.96202199,11.7173929,12.44424886,13.1371727,13.7928253\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.582612441,10.3763395,11.15369342,11.91072236,12.64275498,13.34549302,14.015573\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.244772782,10.11015867,10.95723847,11.77857287,12.56764138,13.31947731,14.03081574\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.595959943,10.38796888,11.16395177,11.91987501,12.65100386,13.35299204,14.02244022\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.24403203,10.10938504,10.95643391,11.77774266,12.5667924,13.31861684,14.02995081\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.570724766,10.36573196,11.1441721,11.90212883,12.63495969,13.33838957,14.0090734\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,9.246321584,10.11146056,10.95830023,11.7794127,12.56828325,13.31994706,14.03113871\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.50316734,15.3300242,16.07421888,16.74486326,17.35020425,17.89755083,18.3933189\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.22702203,15.08264806,15.85061463,16.54118658,17.16347452,17.7254316,18.23395396\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.51975492,15.33927706,16.07756117,16.74337293,17.34474727,17.88885116,18.38199446\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.63128695,15.4442431,16.17582155,16.83512118,17.4303414,17.9687159,18.45656777\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.54433944,15.36543791,16.10444605,16.77044533,17.37166343,17.91538558,18.4079959\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.66958078,15.47947135,16.20712097,16.86220103,17.45325608,17.98771596,18.47200398\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.26118677,15.11819429,15.88708557,16.57815486,17.20056504,17.76232834,18.27039904\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.1330199,14.99458984,15.76977093,16.46792212,17.09762924,17.66656174,18.18148074\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.50514557,15.33221046,16.07645646,16.74706088,17.35231124,17.89954145,18.39518254\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.1843113,15.0443764,15.81618877,16.51010143,17.1353008,17.69980447,18.21056295\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.51668746,15.33694463,16.07580155,16.74206077,17.34378517,17.88816313,18.38152106\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.6436643,15.45472986,16.18485268,16.84300623,17.43730518,17.9749252,18.46214892\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.55167504,15.37195088,16.11024442,16.77562105,17.37629568,17.91954287,18.41173757\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.65889377,15.46992278,16.19857682,16.85453454,17.44635344,17.98147779,18.46634477\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.24335187,15.10166943,15.87180997,16.56404323,17.1875238,17.7502644,18.2592242\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.20810705,15.06055968,15.82813171,16.51987269,17.14413381,17.70840416,18.21930433\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.50876757,15.33440651,16.0776966,16.74765835,17.35247662,17.89941754,18.39486692\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.24903606,15.10196508,15.86768403,16.55636389,17.17704483,17.73762633,18.244963\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.52606827,15.34470272,16.08230007,16.74756821,17.34850264,17.89224321,18.38508096\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.62997943,15.44364196,16.175679,16.8352719,17.43067487,17.96915827,18.45706981\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.5491943,15.36972639,16.1082543,16.77384615,17.37471767,17.9181437,18.41049961\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.6660031,15.47594106,16.20372386,16.85897879,17.45022502,17.98487808,18.46935348\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.23226812,15.09215683,15.8635886,16.55689547,17.18127686,17.74477872,18.25438557\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])N1CCN(C(C1)C)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Cu][Cu], topology acs\",,,14.16945429,15.02651019,15.79794642,16.49295866,17.12001021,17.68667725,18.19964896\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,20.92732036,21.31460831,21.62070141,21.86637573,22.06628289,22.2309576,22.36811074\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,20.87857529,21.27337467,21.58542528,21.83588926,22.03969602,22.20758267,22.34740944\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,20.93120545,21.3180193,21.62369962,21.86902002,22.06862526,22.23304247,22.36997539\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,20.91014798,21.30012897,21.60834079,21.85570917,22.05699035,22.22279379,22.36088468\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,20.84493804,21.24494324,21.56111791,21.8148939,22.02139463,22.19149834,22.3331693\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,20.94478034,21.32919412,21.6330497,21.87695378,22.07543942,22.23895719,22.37515714\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,3.356831043,4.045310318,4.75101133,5.4567571,6.149536397,6.820271445,7.463236737\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,3.355078929,4.043392829,4.749015562,5.454743236,6.147544691,6.818327927,7.461357504\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,3.356069775,4.044519281,4.750226901,5.45600255,6.148824948,6.81960927,7.46262538\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,3.35588253,4.044095709,4.749591813,5.455185943,6.147858896,6.818525255,7.461452512\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,3.35529971,4.043609147,4.749222564,5.454938524,6.147727267,6.818497633,7.461514697\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,3.354600654,4.043066256,4.748789439,5.454585546,6.147435096,6.818253145,7.461308552\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,6.660600489,7.454826189,8.246226678,9.02818753,9.795017492,10.54179073,11.26438293\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.767825614,8.563605965,9.350476617,10.12356493,10.87774543,11.6082972,12.31130262\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.331024375,8.190140969,9.029897656,9.846567055,10.63660063,11.39678375,12.12446727\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,9.257091014,10.07292149,10.85658965,11.6054277,12.3178,12.99287828,13.63049611\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,6.658002445,7.452657796,8.244576239,9.027066066,9.794392126,10.54160679,11.26457772\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.770335345,8.565701604,9.352232954,10.12504364,10.87899611,11.60935958,12.31220867\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.326357257,8.185774066,9.02588314,9.842915925,10.63329879,11.39380418,12.12177794\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,9.250136265,10.06588453,10.84969712,11.5988217,12.31156122,12.98704498,13.62507848\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,6.65616887,7.450455947,8.241993721,9.024133086,9.791161673,10.53814071,11.26093797\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.762909433,8.559300365,9.346695933,10.12023235,10.87479407,11.60567,12.30895156\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.32557885,8.184765335,9.024621239,9.841417129,10.63159926,11.39194719,12.11980638\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,9.253657297,10.06988628,10.85394465,11.60314489,12.3158425,12.99120697,13.62907325\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,6.661575478,7.45578961,8.24722189,9.029234511,9.796120587,10.54294494,11.26557843\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.769519533,8.564998001,9.351555289,10.12434143,10.87824425,11.60854947,12.31134166\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.330768953,8.19041232,9.03047428,9.847291042,10.63736434,11.39751767,12.12512967\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,9.260413744,10.07581983,10.8591495,11.60770689,12.31984067,12.9947132,13.63215198\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,6.651447692,7.448237835,8.241795332,9.025531457,9.793794692,10.54170522,11.26518516\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.772345517,8.568045899,9.354831039,10.12783159,10.88192182,11.61237973,12.31528683\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.326314391,8.184884215,9.024347123,9.840897671,10.63093061,11.39119162,12.11900429\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,9.249088032,10.06458282,10.84817744,11.59712123,12.30971529,12.98508593,13.62303527\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,6.65621939,7.451566655,8.243854361,9.026515652,9.793895832,10.54109849,11.26402339\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.762749723,8.55888867,9.346104421,10.11951645,10.87399658,11.60482382,12.30808162\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,7.324043022,8.183630608,9.023803606,9.840843241,10.6312088,11.39169245,12.11965066\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,9.247712102,10.06469975,10.84934936,11.5990225,12.31210745,12.98779591,13.62593813\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.71992058,15.50982195,16.2212422,16.86325505,17.44370395,17.96937106,18.44614959\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,15.25199933,15.97107034,16.61998676,17.20687984,17.73889672,18.22221103,18.66213277\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.48098353,15.44382531,16.28914413,17.03326988,17.69028146,18.27215584,18.7890418\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.88184404,15.65234644,16.34713168,16.9748893,17.54310969,18.05826333,18.52597526\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,15.24577718,15.96567641,16.61497556,17.2020308,17.7341113,18.21745529,18.65740531\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.42117642,15.39021829,16.24062146,16.98904031,17.64975689,18.23487946,18.75464514\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.72953303,15.51297173,16.22036189,16.85989591,17.43886273,17.96369148,18.44004811\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,15.24092984,15.9618185,16.61209033,17.20002323,17.73285822,18.21683078,18.65729276\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.35813802,15.33347323,16.1901984,16.94452061,17.61054342,18.20033608,18.72416438\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.77614815,15.55926774,16.26480917,16.90175424,17.47784525,17.99976568,18.47331866\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,15.26039757,15.97886108,16.62705131,17.21320146,17.74451096,18.22717745,18.6665193\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.35786452,15.33434903,16.19115292,16.94505385,17.61046638,18.19962169,18.72286385\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.85160595,15.62599811,16.32428328,16.95511132,17.52598569,18.04341402,18.51306693\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.96270509,15.71415868,16.39028679,17.00030135,17.55214686,18.0526029,18.5074493\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.57740609,15.52848308,16.36357498,17.09890282,17.74837808,18.32380085,18.83515511\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.75211409,15.53751814,16.24524104,16.88419117,17.46208592,17.9856093,18.46057726\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,15.18733946,15.91585093,16.57196471,17.16450965,17.70108097,18.18814777,18.63121993\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Mn], topology pcu\",,,14.36343376,15.33615495,16.1909201,16.94379311,17.60876054,18.19779879,18.7211012\n\"linker [C]#N, nodes [Cd], topology pts\",,,19.73465906,19.9233947,20.07160485,20.18988525,20.28564645,20.36417735,20.42932316\n\"linker [C]#N, nodes [Cd], topology pts\",,,19.7351899,19.92394094,20.07216363,20.19045431,20.28622402,20.36476201,20.42991379\n\"linker [C]#N, nodes [Cd], topology pts\",,,19.33372102,19.49138051,19.61494058,19.71341811,19.79307437,19.85835591,19.91248445\n\"linker [C]#N, nodes [Cd], topology pts\",,,19.34746802,19.50513924,19.62870773,19.72719148,19.80685243,19.87213759,19.92626898\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.414478284,7.822033858,8.211605187,8.58744198,8.95204902,9.306541018,9.651089452\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.329910698,7.737497527,8.127040491,8.502816965,8.867346643,9.221752292,9.56620984\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.237683061,7.640856071,8.024745663,8.394117339,8.751832768,9.099249801,9.436704192\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.416279193,7.823865374,8.213463209,8.589324081,8.95395359,9.308466818,9.653035399\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.332391831,7.739994916,8.129552448,8.505342686,8.869885677,9.224304288,9.568774428\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.241602702,7.644766236,8.028628105,8.397961594,8.755633317,9.103004259,9.44041216\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.415734878,7.823318192,8.212908843,8.588758604,8.953373765,9.307870178,9.652420203\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.329720587,7.737304922,8.126849739,8.502630614,8.867166044,9.221578034,9.566042039\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.237791428,7.640980834,8.024884498,8.394267932,8.751992933,9.099417544,9.43687775\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.414239597,7.821851278,8.211469215,8.587345865,8.951987654,9.306510332,9.651086077\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.329353943,7.736976884,8.126549272,8.50235039,8.8669011,9.221324931,9.56579834\n\"linker [C]#N, nodes [Cd], topology pts\",,,7.239022501,7.642202287,8.026079686,8.395427553,8.753112291,9.100494832,9.437912952\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.27785888,17.6986422,18.03605201,18.31363258,18.54848823,18.75309178,18.93650563\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.23429148,17.66260811,18.00610792,18.28864576,18.5275644,18.73551983,18.92171605\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.27657365,17.69736702,18.03478346,18.31236827,18.54722645,18.75183126,18.93524544\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.23617304,17.66418297,18.00743684,18.28977533,18.5285307,18.73635108,18.9224346\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.27760912,17.69842145,18.03585609,18.31345785,18.54833163,18.75295077,18.93637809\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.23406134,17.66242814,18.00596762,18.28853671,18.52747984,18.7354543,18.92166517\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.27711666,17.69796309,18.03542311,18.31304423,18.54793313,18.75256433,18.93600145\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.23486178,17.6631045,18.00654426,18.28903268,18.52791009,18.73583071,18.92199723\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.56109317,18.88209998,19.14086675,19.3548531,19.53686876,19.69632261,19.84008135\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.54002969,18.8703878,19.13661633,19.3566287,19.54356502,19.70707836,19.85421856\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.97513355,18.33170578,18.63992563,18.91040286,19.15064791,19.36606358,19.56062208\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.55825684,18.87893438,19.13744477,19.35122774,19.53307935,19.69239891,19.83604627\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.54010707,18.87049591,19.13674914,19.35678149,19.54373407,19.70726068,19.85441179\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.96313053,18.31964955,18.62782269,18.89825902,19.13846825,19.35385249,19.54838333\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.56040492,18.88141885,19.14019297,19.35418641,19.53620872,19.69566872,19.83943311\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.53893129,18.86917024,19.13530353,19.35523913,19.54211314,19.70557557,19.85267395\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.96789806,18.32448763,18.63272267,18.90321289,19.14346886,19.3588936,19.5534596\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.56162734,18.88229993,19.14080767,19.35458959,19.53644138,19.69576205,19.83941122\n\"linker [C]#N, nodes [Cd], topology pts\",,,18.54080048,18.87144203,19.13789121,19.35807882,19.54515683,19.70878659,19.85602385\n\"linker [C]#N, nodes [Cd], topology pts\",,,17.97896851,18.33551987,18.64371953,18.91417775,19.15440516,19.36980458,19.56434819\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,19.65065402,19.98735802,20.25185143,20.46310387,20.63432501,20.77491491,20.89169555\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,18.80716497,19.25381132,19.60982827,19.89759509,20.13315687,20.32820108,20.49137335\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.352173466,4.006279091,4.679722255,5.357163279,6.026274983,6.677976002,7.306168457\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,2.724829009,3.344218334,3.996350657,4.664034088,5.332933273,5.992037372,6.633522079\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.152794775,3.832237261,4.529985612,5.229298785,5.917266959,6.584679784,7.225540075\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.301569725,3.953782297,4.628256166,5.30901174,5.982970322,6.64037127,7.27458217\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.506630656,4.157492165,4.825632341,5.496496918,6.158340257,6.802496675,7.42315465\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,2.57245025,3.197521195,3.857472908,4.533989094,5.211976789,5.879943029,6.529775327\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.31408068,3.982910838,4.668760399,5.355989938,6.032366566,6.689064613,7.320281151\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,3.064080801,3.71793983,4.397977612,5.086926593,5.770701183,6.43878853,7.08401617\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.601486245,9.452968691,10.2623708,11.03044848,11.75791626,12.4454989,13.09402573\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.635727882,9.504958579,10.3305087,11.11260311,11.85176474,12.54873488,13.20448465\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.787015808,9.646921055,10.46091723,11.23037436,11.95665968,12.64110149,13.28504551\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.669133608,9.492344166,10.27591926,11.02091287,11.72816907,12.39840494,13.03233576\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.72235014,9.553031086,10.34421712,11.09653409,11.81045645,12.48645097,13.12510342\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.741386603,9.613964516,10.44117839,11.22358754,11.96198654,12.65734553,13.31083007\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.727239363,9.581908523,10.39227559,11.15949148,11.88469943,12.5690144,13.21358896\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,8.545492412,9.398440522,10.20743922,10.97377554,11.69874082,12.38354521,13.02937253\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.380356874,8.139604567,8.887897413,9.622860539,10.34134044,11.03996138,11.7155695\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.876677506,8.583818694,9.286768391,9.983751639,10.67103977,11.34421331,11.99899032\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,6.29591467,7.113345606,7.929559388,8.73603982,9.525862922,10.29338825,11.03415392\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,6.786482095,7.513986802,8.246200107,8.977880841,9.703116629,10.41603751,11.11134269\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.361792322,8.121493055,8.86899758,9.602267524,10.31850656,11.01464764,11.68777311\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,7.833024748,8.552014512,9.26418178,9.968165626,10.66066035,11.33762944,11.99511622\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,6.339386419,7.157132469,7.972371409,8.776834143,9.563891465,10.32818453,11.06548948\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,6.742066572,7.472846058,8.207843698,8.941887154,9.669136725,10.383792,11.08061358\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.607921164,10.46338924,11.30174008,12.11387564,12.89204688,13.63062492,14.32616273\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,10.07450321,10.88068149,11.66657857,12.42655656,13.15521237,13.84831525,14.50309666\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.612689286,10.39247569,11.1631286,11.91736166,12.64796237,13.34894975,14.01599425\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.890484863,10.72831027,11.54081729,12.32310776,13.07043793,13.77914796,14.44695759\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.601297661,10.46209539,11.30473079,12.12025152,12.90104837,13.64161918,14.33862858\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,10.06499294,10.87638682,11.66667633,12.43022755,13.16170048,13.85695748,14.51333249\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.781593198,10.56257976,11.33435503,12.08904429,12.81914315,13.5185941,14.18312646\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,9.860417489,10.70006933,11.51452062,12.29878403,13.04804571,13.75859739,14.42812964\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,14.22604442,15.05695838,15.7950836,16.45417422,17.04535537,17.57765039,18.05845306\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,14.65131595,15.42536786,16.11550362,16.73401023,17.29076244,17.79374812,18.24951086\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,14.28972961,15.09803764,15.81825319,16.4631514,17.04311817,17.56660473,18.0405513\n\"linker [O-]C(=O)c1ccc(cc1)C1=NN=N[N]1, [O-]C(=O)c1ccc(cc1)C1=N[N]N=N1, nodes [Cu], topology pcu\",,,14.48061367,15.27022517,15.97467038,16.60615451,17.17458319,17.6880281,18.15313809\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,14.62890768,15.28554694,15.83400487,16.2946368,16.68380551,17.01459768,17.29746974\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,16.09647923,16.68336367,17.16778013,17.57066834,17.90830173,18.19335058,18.43572066\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,4.088466547,4.814882843,5.541511359,6.253386138,6.939997402,7.594690653,8.213903149\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,4.562430616,5.062538197,5.496454498,5.87139557,6.195115522,6.474958631,6.717476575\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,2.437179765,3.000929413,3.607638961,4.239986948,4.882887976,5.524341966,6.155502128\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,2.459532084,2.987166974,3.542490405,4.112984594,4.687768659,5.258036837,5.817125915\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,4.28377926,5.169020771,6.030691855,6.85163712,7.622190081,8.338193103,8.999288372\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,3.26961344,3.954526432,4.65323671,5.349103596,6.029570321,6.685943524,7.312820752\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,3.346854435,4.03582893,4.73982718,5.441429669,6.127628694,6.789524209,7.421665559\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,3.163819041,3.828282189,4.513201959,5.201277184,5.879094372,6.53709154,7.16907422\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,3.524587347,4.241380194,4.967545827,5.686298116,6.385404185,7.056688692,7.69530749\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,3.941004915,4.682075595,5.416913059,6.131552578,6.816270033,7.464925295,8.074194301\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,9.42048557,10.16002295,10.85786394,11.51416017,12.13034204,12.70843283,13.2506579\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,7.952681108,8.650652683,9.32124443,9.96488887,10.58181221,11.17208098,11.73571232\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,6.069369319,6.671403875,7.254352314,7.815733287,8.354772834,8.871579858,9.366647991\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,7.253025232,7.992206237,8.710964322,9.405492768,10.07289692,10.71108549,11.31870016\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,8.188490178,8.95457976,9.695887285,10.40740795,11.08601532,11.73001095,12.33876701\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,8.047831031,8.801179058,9.528121416,10.22596322,10.89281958,11.52751138,12.12948222\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,8.126946535,8.967635891,9.783203089,10.56665399,11.31322822,12.02004373,12.68573975\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,7.363061268,8.153629147,8.92385325,9.667262389,10.37919273,11.05653068,11.69747057\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,6.963993547,7.76299555,8.565764509,9.361017869,10.13903007,10.89206616,11.61444201\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,6.334900718,7.141725451,7.936900067,8.714569288,9.470525616,10.20156209,10.90520129\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,7.833197608,8.585697187,9.32268249,10.041635,10.73975437,11.41436357,12.06317301\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,6.258375323,7.08539385,7.910867154,8.72488508,9.519507828,10.28854231,11.02737931\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,7.523988461,8.185521525,8.83147005,9.464014271,10.08350041,10.68903723,11.27906064\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,5.538936441,6.336010265,7.141593816,7.944850373,8.736520133,9.508949919,10.25611124\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,7.872962577,8.617318425,9.347905182,10.06232434,10.75771436,11.43122316,12.08032989\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,6.446623143,7.272799421,8.100746247,8.920065509,9.72221057,10.50039407,11.24948484\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,13.29729035,14.11539026,14.85242295,15.51779471,16.1199719,16.66635123,17.16330463\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,14.56709139,15.33883649,16.02592,16.64133796,17.19525425,17.69574472,18.14935124\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,12.12163094,12.83648546,13.48219921,14.06621597,14.59510398,15.07463468,15.50989484\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,14.56546624,15.34906132,16.05086338,16.68156927,17.24981541,17.76277498,18.22655245\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,13.59691713,14.4574525,15.22985921,15.92394074,16.54846326,17.11119243,17.61898165\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,14.09815479,14.90595063,15.62598933,16.27100379,16.85134059,17.37542818,17.85019297\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,14.66440346,15.36659543,15.99910287,16.57114943,17.0903097,17.56279863,17.99377123\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,11.59382101,12.28564969,12.9088115,13.4721735,13.98286018,14.44672583,14.86870213\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,13.24196375,14.39303885,15.38882796,16.24840946,16.9905746,17.63249151,18.18922388\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Fe], [OH], topology rna\",,,13.3556819,14.48446401,15.46325732,16.31128102,17.04675404,17.68601765,18.24329708\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,20.45032929,20.87314686,21.21129348,21.4853171,21.7100578,21.89639926,22.05244112\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,20.46124482,20.88331228,21.22062136,21.49381677,21.71778143,21.90341521,22.0588208\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,20.45452868,20.87773631,21.21591312,21.48978544,21.71428917,21.90035975,22.05612452\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,20.45025815,20.87308752,21.21124307,21.48527365,21.7100199,21.8963659,22.05241151\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,20.4615369,20.88355424,21.22082508,21.49399065,21.71793159,21.90354619,22.05893606\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,20.45364513,20.8769897,21.21527476,21.48923393,21.71380828,21.89993698,22.0557501\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,3.298907676,4.000519067,4.718119709,5.434256376,6.135845386,6.813860407,7.462693527\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,3.297558596,3.999198916,4.716823974,5.432983767,6.134597094,6.812639078,7.46150237\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,3.301772514,4.003088893,4.720397266,5.43626109,6.137603887,6.815401142,7.464043911\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,3.298883245,4.000488463,4.718083726,5.434215942,6.135801448,6.813813862,7.462645181\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,3.297651843,3.999299996,4.716930688,5.433094164,6.134709503,6.812752107,7.461614888\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,3.301838411,4.003163719,4.720479616,5.436349424,6.137696672,6.815496949,7.464141475\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,6.666966453,7.466795426,8.26000152,9.041360918,9.806184851,10.55024616,11.26988789\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.678996237,8.483519684,9.277978375,10.0576211,10.81749073,11.55303197,12.26046869\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.348852957,8.208454276,9.049650501,9.86856872,10.66136433,11.42452588,12.15516612\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,9.204762496,10.04542627,10.848533,11.61254324,12.33671753,13.02093156,13.66557005\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,6.671739003,7.468563001,8.259430568,9.039012066,9.802518889,10.54563393,11.26462245\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.679742536,8.483924536,9.278100546,10.05752152,10.81722389,11.55264325,12.25999432\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.34042396,8.200191172,9.041588224,9.860740507,10.6537971,11.41723898,12.14817165\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,9.19315253,10.0346122,10.83848401,11.60321826,12.32807061,13.01291488,13.6581359\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,6.673573497,7.47331842,8.26632135,9.047404778,9.811916156,10.55565305,11.27497396\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.690501083,8.494668723,9.288638104,10.0677392,10.82705823,11.56206208,12.26898519\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.343627895,8.203751153,9.045395296,9.86470395,10.65784344,11.42130998,12.15222207\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,9.210140933,10.05035228,10.85300708,11.61658758,12.34036519,13.0242198,13.66853646\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,6.666856533,7.466715745,8.259944114,9.0413198,9.80615555,10.55022536,11.26987315\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.679205833,8.48372378,9.278175363,10.05781015,10.81767146,11.5532043,12.26063271\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.348841771,8.208454872,9.049660993,9.868587427,10.66138974,11.42455664,12.15520104\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,9.204689882,10.04536183,10.84847584,11.61249245,12.3366723,13.02089115,13.66553381\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,6.671640026,7.468476198,8.259354252,9.038944627,9.802458893,10.54558016,11.26457388\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.679648231,8.483838017,9.278021247,10.05744878,10.81715704,11.55258169,12.2599375\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.340485962,8.200251693,9.041647686,9.860799249,10.65385532,11.41729675,12.14822892\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,9.193124193,10.03458877,10.83846539,11.6032043,12.32806105,13.01290937,13.65813404\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,6.673604373,7.473333068,8.266323923,9.047398369,9.811903102,10.55563514,11.27495257\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.690543766,8.494714441,9.288685959,10.06778853,10.82710849,11.5621128,12.26903598\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,7.343600366,8.203727288,9.045374411,9.864685695,10.65782759,11.42129637,12.15221051\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,9.210113346,10.05032828,10.85298679,11.61657099,12.34035217,13.02421012,13.66852981\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.35466172,15.17223778,15.90669297,16.56876973,17.1672647,17.70950474,18.20169628\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.1230422,14.97607514,15.73745514,16.4196504,17.03310848,17.58654673,18.08726003\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,13.7598468,14.82309016,15.75455281,16.572067,17.29140094,17.92616239,18.48796968\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.27247768,15.09718829,15.83824692,16.50636697,17.11034729,17.65753783,18.15418061\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.36657917,15.18990697,15.92685178,16.58869591,17.18500793,17.72384736,18.21201163\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,13.6938971,14.76353725,15.70097751,16.52391763,17.2480964,17.88714472,18.45272793\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.09907472,14.93900179,15.69435679,16.37555749,16.99133282,17.54907672,18.05512693\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.32162442,15.1517438,15.8936519,16.5592327,17.15844856,17.69961681,18.18970441\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,13.68175206,14.7512944,15.68894194,16.51227303,17.23694681,17.87654244,18.44269195\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.35267204,15.17045913,15.90509628,16.56733013,17.16596116,17.70831955,18.20061456\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.12104172,14.97427408,15.73582961,16.41817923,17.03177318,17.5853312,18.08615031\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,13.75900572,14.82231522,15.75384312,16.57141906,17.29081003,17.92562339,18.48747753\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.27337544,15.09799995,15.83898286,16.50703614,17.11095737,17.6580955,18.15469167\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.36588119,15.18929341,15.92630712,16.5882084,17.1845685,17.7234489,18.21164844\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,13.69424486,14.76386538,15.7012846,16.52420365,17.24836209,17.88739121,18.45295655\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.10094627,14.94069264,15.69589126,16.37695537,16.99261051,17.55024803,18.05620361\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,14.3214576,15.15156679,15.89347285,16.55905676,17.15827881,17.69945497,18.18955131\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Cu], topology pcu\",,,13.68032869,14.75000047,15.68777038,16.51121366,17.23598852,17.87567433,18.4419039\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,19.70082441,19.99901993,20.23721147,20.43012041,20.58829318,20.71942855,20.82924082\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,19.71972199,20.00738,20.23738963,20.42382384,20.57678808,20.70367319,20.80997335\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.28890899,3.883261253,4.505979612,5.141753105,5.777852694,6.404498208,7.014727185\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.472907389,4.136407289,4.821488843,5.510245506,6.188986735,6.848067029,7.481307394\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.529568246,4.191838782,4.874923299,5.561265661,6.237416926,6.893888272,7.524595688\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,2.992037233,3.567794139,4.179506626,4.811065863,5.448650951,6.081358831,6.701207355\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.453559076,4.114535667,4.796740558,5.482537411,6.158420334,6.814854122,7.445714341\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.312900128,3.906876771,4.528360705,5.162298553,5.796173581,6.420369163,7.028043111\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,2.914754136,3.485666339,4.094859821,4.725938954,5.364690606,5.999817747,6.622992644\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.523072793,4.183310949,4.864432914,5.549032028,6.223737752,6.879086987,7.508987083\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.350476601,3.945750164,4.568519083,5.203622585,5.838487653,6.463476938,7.071750145\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.481165351,4.144628183,4.82957629,5.518126447,6.196608542,6.855393443,7.48831464\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.47876799,4.13845038,4.819861234,5.5053649,6.18140355,6.838375105,7.470090566\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,2.951409436,3.524402272,4.134588826,4.765712274,5.403727211,6.037497134,6.658832527\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.502102425,4.163664515,4.846436323,5.532799276,6.209243123,6.866221446,7.497598922\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.288978321,3.883059757,4.50540421,5.140807419,5.776604389,6.403046813,7.013182175\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.020762074,3.598131959,4.210413274,4.841699611,5.478366132,6.109682905,6.727811955\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,3.509714228,4.17029884,4.85153158,5.53604539,6.210502581,6.865469179,7.494879182\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,8.982629206,9.684401228,10.37896877,11.05995785,11.7219089,12.36047729,12.97247066\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.298473484,10.0227934,10.73025133,11.41627491,12.07709624,12.70988107,13.31272383\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,7.196630971,7.969055444,8.736125049,9.492133621,10.23173661,10.95017786,11.64350213\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.35208297,10.07974703,10.79030216,11.47917325,12.14260293,12.77777169,13.38278938\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.077737765,9.780473521,10.47510157,11.15577183,11.8173036,12.45548393,13.06717278\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,7.159153945,7.930434565,8.69635952,9.451328974,10.1900175,10.90765006,11.60024132\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.333154222,10.05929534,10.76844715,11.45608204,12.11844548,12.752702,13.35693981\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.032764622,9.738867164,10.43667654,11.12010554,11.78390364,12.42387786,13.03694616\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.091344192,9.794002023,10.48763386,11.16686727,11.82682782,12.46348547,13.07379969\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.357950782,10.08673926,10.79856563,11.48877347,12.15353058,12.78996098,13.39613779\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,15.03564897,15.71926371,16.29341876,16.78256171,17.20599252,17.57863623,17.91183628\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,8.927455122,9.624386847,10.31552919,10.99414914,11.65452214,12.29210603,12.90355972\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.274509702,9.997454186,10.70395326,11.38932111,12.04969875,12.6821835,13.28482057\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,7.153726034,7.927147151,8.695574381,9.453111402,10.19427773,10.91422691,11.60894885\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.269039052,9.997142648,10.708305,11.39789618,12.06209528,12.698029,13.30376884\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,8.962732886,9.663763336,10.35681443,11.03615867,11.69666544,12.33412502,12.94537381\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,7.137660408,7.908634516,8.674234247,9.428850763,10.16717523,10.8844558,11.57672777\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.030002691,9.749524723,10.4531638,11.13615398,11.7945612,12.42541615,13.02670668\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,8.727132183,9.426459864,10.11926045,10.79899964,11.46009944,12.09812483,12.70981308\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,8.875856676,9.579755354,10.27528523,10.95667015,11.61878243,12.25744725,12.8695516\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,9.120780886,9.848366509,10.55888879,11.24780898,11.91137222,12.54674547,13.15201958\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,15.02315328,15.71152614,16.28977589,16.78242243,17.20884767,17.58405443,17.91945469\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,10.51082309,11.25818551,11.98141443,12.67725644,13.34277202,13.97571992,14.5746894\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,10.44265621,11.19261176,11.91776872,12.6151013,13.28182325,13.91579246,14.51566032\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,15.7088988,16.2055302,16.6142485,16.95734904,17.25177048,17.51022764,17.74213516\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,10.53809311,11.27207803,11.98323588,12.6682404,13.32408578,13.9484574,14.53986154\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,10.55271513,11.28939081,12.00215004,12.68801629,13.34423753,13.96867744,14.55996418\n\"linker N#N, [C]#[C], n1ccc(cc1)c1ccncc1, nodes [Cu], topology dia\",,,15.67501393,16.18855654,16.61085036,16.96494041,17.26832562,17.53414185,17.77212348\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.26978563,21.64565587,21.94387119,22.18397767,22.37986045,22.54156531,22.67648419\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,19.6174769,19.99441413,20.29272579,20.53240833,20.72760951,20.88852612,21.02263509\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.42124372,21.79678801,22.09483368,22.33485959,22.53071283,22.6924173,22.82735215\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.39992929,21.74617093,22.02032843,22.24069553,22.42022855,22.56827333,22.69168738\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.43694833,21.78999543,22.07028555,22.29608598,22.48038594,22.6325917,22.7596303\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.39787701,21.74390341,22.01806629,22.23858006,22.41834233,22.56665902,22.69036181\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.00817747,21.37847911,21.67229953,21.90884686,22.10179327,22.26104137,22.39388181\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.18927201,21.55643464,21.84679961,22.07997985,22.26981794,22.42627362,22.5566409\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.218958821,3.873589996,4.554800032,5.244359256,5.927789617,6.594525239,7.237515677\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.421427567,4.08534896,4.771737937,5.462920753,6.145034008,6.808107573,7.445625767\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.386712239,4.053286408,4.742928631,5.437630378,6.123286769,6.789769862,7.430471575\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.25488182,3.916685645,4.604028722,5.298489976,5.985563151,6.654752459,7.299127797\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.428292854,4.094259168,4.783070261,5.476792135,6.161388592,6.826787486,7.466421955\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.377041272,4.042750025,4.732074244,5.426890366,6.113003214,6.780218244,7.421879975\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.212034051,3.870357285,4.554694789,5.24677141,5.932122911,6.600233808,7.244122428\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.355504482,4.014815423,4.698360735,5.388272597,6.070446931,6.734671025,7.374208084\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.40155987,4.06835761,4.758127074,5.452843921,6.138407907,6.804706933,7.445152932\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.240702501,3.901708768,4.58835935,5.282263714,5.968936285,6.637895654,7.282221434\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.423667534,4.088478511,4.776330594,5.469291193,6.15330885,6.818288533,7.457638399\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,3.3726656,4.039213961,4.729174794,5.424394424,6.110666208,6.777795293,7.419132289\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.509007257,7.278861633,8.049030404,8.812843511,9.564398828,10.2984954,11.01071584\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.799156374,8.569087575,9.326870293,10.06997942,10.79516684,11.49900047,12.17831542\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.230149103,10.00361159,10.75675761,11.48475068,12.18373566,12.85097245,13.48477891\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.72383143,8.490676075,9.243781654,9.981415256,10.70091466,11.39924777,12.07349915\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.16661157,9.941136076,10.69527304,11.42416152,12.12383307,12.79143108,13.42519032\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.680764231,8.465004537,9.236506314,9.992427563,10.72929156,11.44353067,12.13192912\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.163700509,9.948314713,10.71235362,11.45058904,12.15882686,12.8340916,13.47457724\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,5.767789671,6.544258753,7.317691071,8.081815329,8.831540527,9.562524761,10.27108505\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.463242498,7.251192406,8.035383951,8.809393797,9.567983023,10.30672087,11.02190307\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.528959101,7.309351266,8.086918948,8.85581027,9.610730954,10.34693882,11.06036438\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.778149806,8.551471106,9.312265063,10.05791061,10.78515959,11.49062682,12.1712119\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.206200523,9.981785688,10.73768411,11.46869911,12.17073323,12.84088932,13.47738963\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.862154294,8.633841168,9.392399871,10.13557812,10.86037359,11.56354975,12.24208539\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.313485924,10.09189935,10.84951135,11.58145689,12.28378911,12.9536868,13.58942548\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.780830121,8.567752777,9.341407544,10.09903999,10.83725319,11.55254798,12.24176562\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.239827639,10.02388639,10.78710237,11.52434406,12.23150316,12.90567262,13.54509648\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.674952666,7.458122878,8.235895464,9.002853614,9.754414914,10.48654723,11.19576332\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.609115174,7.409529983,8.203484106,8.985113189,9.74959636,10.49282699,11.21135958\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.634559041,7.426494615,8.213817531,8.991006585,9.752992472,10.49519918,11.21369058\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.665475146,8.440478644,9.202450469,9.948962169,10.67687045,11.382847,12.06382344\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,8.969968086,9.746668291,10.5025174,11.23277334,11.9336576,12.60249163,13.23764298\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.66259469,8.429215643,9.182121006,9.919551988,10.63884338,11.33696859,12.0110194\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.179526912,9.956068203,10.71182429,11.4420435,12.1428425,12.81142844,13.44608221\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.678956818,8.464724906,9.237418947,9.994198319,10.73161544,11.44614604,12.13462209\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.181563395,9.963519806,10.72438775,11.45922317,12.16403184,12.83597283,13.47332484\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,5.901689896,6.679251182,7.451861164,8.213972869,8.961024499,9.689049755,10.39462192\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.417852428,7.202845776,7.985280368,8.758377642,9.516596106,10.25526027,10.97048065\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,5.810957285,6.578025172,7.345960964,8.10799607,8.858146867,9.591143938,10.30251234\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.616274205,8.388421383,9.148334714,9.893324867,10.62009862,11.32524007,12.00562626\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.166748409,9.941203701,10.69603586,11.42608127,12.12726057,12.7966849,13.4325781\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.91236834,8.682392872,9.438906908,10.17988034,10.90246687,11.60353317,12.28012054\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.35106599,10.12833736,10.88489618,11.61585936,12.31727526,12.98632386,13.62128331\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,7.755628717,8.541892938,9.315128761,10.07253211,10.81065634,11.52595895,12.21524659\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,9.147919584,9.930310718,10.69235862,11.42877168,12.13533273,12.80906017,13.44814671\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.428506822,7.213702063,7.99349767,8.76232242,9.515541728,10.24912319,10.95960179\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,6.566396574,7.364112561,8.155995031,8.936023373,9.699269563,10.44154967,11.15936022\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.69017388,21.93913652,22.13425927,22.28970128,22.41535164,22.51825313,22.60351423\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,22.25258256,22.51632847,22.72310241,22.88786708,23.02107964,23.13019142,23.22060968\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.95926127,22.21279011,22.41147455,22.56974277,22.69767013,22.80243111,22.88922918\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,21.81659532,22.07060602,22.26954154,22.42793277,22.55591096,22.66068191,22.74746704\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.35554984,15.15737293,15.87592342,16.52173579,17.10351463,17.62859454,18.10326443\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.4969927,15.19437947,15.81891916,16.38120445,16.88979784,17.35162998,17.77235375\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.18688686,14.93305015,15.60555189,16.21341488,16.76438188,17.26502687,17.72093235\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,10.01526471,10.68996452,11.30495734,11.86539757,12.37643059,12.84285011,13.26899296\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,15.1739685,15.8302946,16.42111849,16.95531776,17.44016988,17.88164036,18.28465698\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,13.94250221,14.82773597,15.61866099,16.3274099,16.964369,17.53836741,18.05691163\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,13.72561451,14.67822214,15.52375562,16.27721369,16.9508483,17.55480639,18.09761437\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.32235777,15.00455008,15.61461387,16.16340918,16.65961461,17.11018401,17.52073832\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.4616483,15.26936683,15.99256478,16.64283168,17.22971233,17.76108453,18.24350108\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.38925007,15.23480741,15.9887457,16.66346929,17.26943452,17.81540923,18.30875546\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.43187507,15.26117449,15.99941624,16.65965586,17.25269131,17.78741826,18.2711862\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,13.90822651,14.79805255,15.5920256,16.30286934,16.94133354,17.51647124,18.0359266\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,13.73603152,14.68538671,15.52735195,16.27731222,16.94774035,17.54889038,18.08932269\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.82511683,15.60179777,16.28999274,16.90424006,17.45586954,17.95379463,18.40511866\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,11.68508224,12.34053909,12.93307705,13.47105129,13.96119974,14.40900346,14.81898933\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,12.97083068,13.81346927,14.56802323,15.24522387,15.85458065,16.40432923,16.90153592\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.01906359,14.8073585,15.51380925,16.1488636,16.72155172,17.2395477,17.70934072\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.726116,15.47399814,16.14649427,16.75282098,17.30085834,17.79732368,18.24796309\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,13.69916589,14.49858563,15.21442171,15.85751853,16.43672522,16.95943663,17.43195897\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,13.02176754,13.69236063,14.29523807,14.83969551,15.33338369,15.78258102,16.19246561\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,12.89095121,13.59002476,14.22129252,14.79337824,15.31343656,15.78741219,16.22028921\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.18658188,15.04450803,15.8109375,16.49787161,17.11552883,17.67254845,18.17623426\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.15025565,15.00127137,15.75934946,16.43744428,17.04642817,17.59535098,18.09174393\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes Cl[Mn], [Mn], topology srs\",,,14.60343446,15.39927163,16.11421666,16.75819972,17.33973429,17.86608798,18.34347866\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,20.63294158,21.08988575,21.45837631,21.75911962,22.00728035,22.21412045,22.3881142\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,21.21251608,21.59739653,21.90162274,22.14591844,22.34485482,22.50888481,22.64564657\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,20.69726556,21.13215835,21.4764717,21.75319414,21.97860523,22.1644476,22.31933793\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,20.46590764,20.92849142,21.29707664,21.59517594,21.8394777,22.04205807,22.21181375\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,20.39468102,20.87279766,21.25929797,21.57537043,21.83661332,22.05466012,22.23829599\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,19.65358797,20.06323533,20.38757156,20.64829742,20.86076362,21.03602952,21.18220128\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,20.77383019,21.26572466,21.65524429,21.96832267,22.22334912,22.43359924,22.60881992\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,20.92766104,21.39662218,21.76988784,22.07154841,22.31864584,22.52347967,22.69509217\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.065781295,2.5907488,3.190133823,3.852320177,4.563405292,5.308959889,6.075271556\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.823925573,3.531831289,4.264731133,5.000680165,5.723574313,6.422609123,7.091285778\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.241568123,3.750293236,4.286994686,4.843647532,5.411524918,5.982474482,6.549624851\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.92361591,3.400460589,3.912171547,4.450523606,5.006206635,5.570262663,6.134925274\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.434974545,3.948022389,4.487003576,5.043951101,5.610299507,6.178110537,6.740745788\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.231908573,3.727076559,4.254358778,4.804870086,5.36907037,5.938114025,6.504572587\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.363774556,3.842912138,4.353219496,4.887200651,5.436113182,5.991484098,6.545983678\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.544149273,4.041549763,4.566782744,5.112079983,5.66881461,6.228869071,6.78538459\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.068139733,3.584726764,4.13145317,4.699136486,5.278231587,5.860043073,6.437364476\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.990383528,3.49410324,4.031495542,4.593118561,5.169025523,5.7500919,6.328709751\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.279478437,3.945442465,4.631473532,5.321006082,6.001111783,6.662482719,7.29900319\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.186127814,3.853007819,4.54170536,5.235064985,5.919675671,6.585868005,7.227272663\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.676191806,4.346459719,5.030111399,5.711959247,6.380485234,7.02763287,7.648308179\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.271398369,3.958914335,4.670466272,5.38640614,6.091606871,6.775411245,7.43103035\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.371885195,4.037662124,4.724207398,5.414493584,6.095248556,6.756950364,7.393377142\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.151779038,3.841176265,4.55599986,5.27622568,5.986388473,6.675554894,7.336723374\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.672609757,4.321299038,4.988401709,5.658019519,6.317883527,6.959242828,7.576403886\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.56777977,4.220205134,4.89124508,5.564692209,6.228101647,6.87263923,7.492588421\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.787933197,3.375832289,3.998180724,4.638843145,5.28409836,5.923159653,6.548134061\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.15149776,3.75034431,4.377564754,5.017908545,5.658632833,6.289905723,6.904698552\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,1.979694077,2.486146776,3.069077576,3.71731403,4.417103028,5.153951204,5.913948047\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.856473735,3.56141112,4.291529899,5.024802799,5.745100783,6.441621019,7.107874662\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.244222975,3.752399551,4.28847752,4.84450202,5.411794516,5.982231669,6.548956223\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.932249826,3.408432044,3.919462773,4.457138857,5.012171063,5.575617903,6.139723805\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.439672459,3.952293011,4.490791654,5.047237422,5.613087657,6.180417486,6.742595545\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.24370964,3.739658574,4.267520656,4.81842888,5.38286817,5.952019865,6.518481241\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.350203746,3.830144435,4.341204252,4.875874056,5.425406187,5.981327277,6.536310204\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.527885122,4.026259367,4.552386234,5.098503352,5.655991051,6.216738817,6.773894271\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.063134965,3.580366696,4.127723126,4.695967735,5.275531638,5.857714769,6.43531684\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.97205726,3.474598811,4.011045769,4.571938914,5.147316021,5.728035052,6.30646797\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.28901441,3.954762067,4.6405458,5.329816108,6.009655528,6.670763201,7.30702789\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.184077969,3.849425193,4.536681501,5.228764629,5.912295325,6.577607621,7.218318845\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.670155129,4.338600781,5.020821591,5.701642821,6.36951602,7.016332387,7.636938675\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.287235621,3.975937815,4.688596406,5.40550756,6.111518518,6.795967765,7.45207545\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.371167539,4.036755453,4.723195158,5.413437402,6.094190787,6.755917967,7.392385626\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.150353905,3.839412241,4.553968223,5.273994985,5.98401946,6.67309876,7.334221858\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.663028214,4.310932797,4.977369111,5.646450897,6.305903406,6.946961307,7.563913677\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.599248321,4.251448742,4.922369243,5.595772447,6.25919089,6.903774434,7.523795646\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,2.756442352,3.340116393,3.959074388,4.597214044,5.240746449,5.878770245,6.503265098\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,3.201008611,3.79964941,4.426676865,5.066858745,5.707460373,6.338651317,6.95340042\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.818509466,7.617475314,8.408859141,9.186259136,9.944667643,10.68009617,11.38941269\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.747252857,8.54347998,9.323285238,10.08454142,10.82452672,11.54034992,12.2293459\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.213551434,10.0024308,10.76593191,11.50074468,12.20413268,12.87413923,13.50961585\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.796616969,8.604471005,9.394564737,10.16447004,10.91130542,11.63216691,12.32448882\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.107864087,9.942858252,10.74632203,11.51553887,12.24826575,12.94301851,13.5991228\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.386979373,8.271706432,9.131360404,9.962771197,10.76317692,11.53020739,12.26200751\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.36249429,10.15193782,10.91821909,11.6568894,12.36436668,13.03814306,13.67675519\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.353916896,7.148039598,7.933760943,8.704676054,9.455941699,10.18378681,10.88529105\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.192786138,10.11879317,11.00993413,11.85724695,12.65515508,13.40098449,14.09430712\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.167966094,7.89401442,8.614805759,9.328046159,10.03060108,10.71890846,11.38941993\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.146129479,10.06369251,10.94795189,11.79042874,12.58552365,13.3303146,14.0240521\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.10500014,7.860787943,8.60909759,9.347551692,10.07290878,10.78154675,11.46992811\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.843388303,7.603431891,8.361325475,9.111558993,9.849247615,10.56997098,11.26984276\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.630005295,7.438822591,8.238199912,9.022521532,9.787433964,10.52935793,11.24534623\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.289467011,10.10562467,10.88983043,11.64020443,12.35513668,13.03355502,13.67500539\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.875623671,8.674643814,9.457008527,10.22064235,10.96276084,11.68038875,12.37079538\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.400743993,10.19034087,10.95488281,11.69114952,12.39622881,13.06793731,13.70493683\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.260122635,8.12079356,8.958207777,9.769801156,10.55325657,11.30642735,12.02747431\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.117975412,9.92013279,10.69433749,11.43815005,12.14936927,12.82637387,13.46822962\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.848475297,8.634824691,9.404520041,10.15602552,10.8869923,11.59474466,12.27671685\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.016936686,9.896425116,10.74859386,11.56557454,12.34163542,13.07327617,13.75895569\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.16467478,7.892647036,8.612521823,9.323374792,10.02306062,10.70866186,11.37700398\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.122345031,10.03199555,10.91328783,11.75590262,12.55298809,13.30079976,13.9980617\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.318739867,8.023526383,8.723885391,9.419172991,10.10685709,10.78337622,11.44487965\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.681563391,8.451600506,9.215287235,9.967596616,10.70357325,11.41867042,12.10903334\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.196498531,9.958024527,10.69816646,11.41402025,12.10283345,12.76232245,13.3908379\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.851914916,10.57383315,11.27804601,11.96036368,12.61740137,13.24663851,13.84638928\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.016246686,9.747572037,10.46342844,11.15966612,11.83249847,12.47882257,13.09635667\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.392074691,10.12362275,10.83730331,11.52856881,12.19377046,12.83021809,13.43614278\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.815879841,7.615480634,8.408059165,9.186993642,9.947089414,10.68421433,11.39513684\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.775439481,8.573076112,9.354325776,10.1169805,10.85826714,11.57526521,12.26529655\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.287936893,10.07671279,10.84003805,11.57463037,12.27777479,12.94752957,13.58275587\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.847286589,8.655650589,9.446316695,10.21683957,10.96431852,11.68583039,12.37879261\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.080581438,9.91367601,10.71551551,11.48336318,12.2149454,12.90874553,13.56405875\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.350346989,8.236373125,9.097412657,9.930204556,10.73192308,11.50015754,12.23303094\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.379330328,10.16949951,10.93664168,11.67624033,12.38465734,13.05934265,13.69880432\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.982141879,7.777585427,8.564855134,9.337372813,10.09019704,10.81950581,11.52235648\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.223817585,10.15042954,11.04178403,11.88908379,12.68685294,13.43247878,14.12557014\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.223203935,7.957032525,8.683847482,9.401750356,10.10791165,10.79900535,11.47166596\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.163706761,10.08191625,10.96659759,11.80928669,12.60440607,13.34906325,14.04254121\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.129055967,7.889665103,8.641656791,9.382914854,10.1103911,10.82060917,11.51014346\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.896533596,7.654709341,8.41108828,9.160130907,9.896920912,10.6170034,11.31645605\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,6.682995931,7.489221666,8.286333209,9.068668698,9.831848954,10.57227797,11.28699426\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.278209231,10.09391513,10.87767259,11.6276579,12.34229012,13.02050882,13.6618607\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.870310045,8.66738978,9.448181055,10.21056533,10.95171531,11.66861646,12.35850281\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.40401504,10.19214267,10.9556284,11.69114782,12.39570576,13.06705504,13.70380974\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.271213497,8.131569414,8.968825017,9.780347163,10.56378418,11.31697266,12.03806527\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.153566354,9.954342546,10.72739759,11.47025638,12.18068916,12.85705095,13.49838734\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.867254048,8.652736927,9.421520458,10.17211289,10.90220822,11.60916337,12.29043313\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,8.973662822,9.850626929,10.70088204,11.51643094,12.29143812,13.02232039,13.70747094\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.066391983,7.789812137,8.50574518,9.213151551,9.909835644,10.59284893,11.25898729\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.08009071,9.990050045,10.87220546,11.71614599,12.51489946,13.2646052,13.96388919\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.328311884,8.038754478,8.743915685,9.443254285,10.1343344,10.81368428,11.47753561\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,7.772524653,8.541803242,9.304891955,10.05673341,10.79234457,11.5071553,12.19729197\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.172571597,9.932723562,10.67191238,11.38720373,12.07578507,12.73530537,13.36405189\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.857562681,10.57902919,11.28288267,11.96491973,12.62173709,13.25079728,13.85040119\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.421695928,10.15360394,10.87000911,11.56677584,12.2401214,12.8869427,13.50495667\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,9.718151323,10.44856684,11.16138494,11.85197876,12.51664289,13.15264858,13.75820116\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,8.502098114,9.545612165,10.54793143,11.50077048,12.39879527,13.23927272,14.02158194\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,8.253347226,9.263503914,10.24086872,11.17650495,12.06405558,12.89964118,13.68152449\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,10.04145651,10.83560585,11.60165482,12.3379214,13.04225099,13.71271758,14.34797414\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,8.437230986,9.482546766,10.48668873,11.44129317,12.34098145,13.18299859,13.96671626\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,8.25920518,9.268813517,10.24613754,11.18209668,12.07022522,12.90656119,13.68930498\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,10.257491,11.05023717,11.81464476,12.54928624,13.25215497,13.92139703,14.55568793\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.5110432,15.35185992,16.10359696,16.77759148,17.38350145,17.92955502,18.42278569\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.30804814,15.08058291,15.78634937,16.43041218,17.01789573,17.55379689,18.04284889\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,10.12836577,10.67978156,11.17845827,11.63215325,12.04711764,12.42834383,12.77981611\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,13.92417901,14.78898612,15.57068306,16.27685097,16.91476033,17.49120859,18.01244885\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.27896677,16.02253054,16.67912685,17.26390843,17.78845607,18.26172452,18.69073976\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,13.77369695,14.61840055,15.38204748,16.07495407,16.70518208,17.27932266,17.80296728\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.54332343,16.23657569,16.85181892,17.40208566,17.89752118,18.34605635,18.75395195\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.09599277,14.91040514,15.65085385,16.32412351,16.93646167,17.49360285,18.00079046\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.07605873,14.89994587,15.6498893,16.33136527,16.95017539,17.51203252,18.02234677\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,16.01030251,16.63920737,17.20354588,17.71369141,18.17743123,18.60075887,18.98840749\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.09307275,14.79889443,15.43767348,16.01700955,16.54352619,17.02293864,17.46017985\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.16429418,14.93759441,15.64036704,16.28020669,16.86379441,17.39695621,17.88476407\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.09510062,15.84720393,16.51783616,17.11983512,17.66302234,18.1551199,18.60235002\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,13.96418698,14.7688153,15.49850447,16.16178614,16.76591242,17.31710829,17.82076138\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.93716778,15.69782799,16.38093047,16.99720545,17.55506769,18.0613488,18.52174906\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.1851531,15.96877067,16.65700688,17.2666448,17.81067445,18.29918805,18.74010509\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.32644437,15.32085608,16.17992801,16.92630588,17.57839682,18.1511288,18.65665287\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.54603087,15.36093156,16.09337839,16.75282054,17.34761253,17.88506955,18.37157701\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.3216622,15.10257408,15.81336384,16.46021469,17.04900321,17.58523059,18.07396875\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,16.2202152,16.78348703,17.29215208,17.75435685,18.17664737,18.56424208,18.92129975\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.20612663,15.04978919,15.81463952,16.5072159,17.13403827,17.70135346,18.21500343\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.90089817,15.7057588,16.4154503,17.04610034,17.61028696,18.11788409,18.57672336\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,13.84888243,14.70227877,15.47101975,16.16629291,16.79684909,17.36982107,17.89122259\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.42084775,16.15556638,16.80573525,17.38559823,17.90627705,18.37648468,18.80310698\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,13.99167584,14.81189763,15.55787043,16.23635616,16.85359082,17.41530777,17.92675687\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,13.81095879,14.65962737,15.4363948,16.14499234,16.79013141,17.37690249,17.91040617\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,16.65576177,17.22692675,17.7429648,18.2124832,18.64183536,19.03586513,19.39838839\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.98062649,15.68524246,16.32301726,16.90153733,17.42739461,17.90627174,18.34307396\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.29601061,15.0513278,15.73990412,16.36844221,16.94297695,17.46885495,17.95078488\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.09693394,15.84368361,16.51226066,17.11423492,17.65862563,18.15264558,18.602193\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.0786272,14.80976511,15.47755767,16.0879784,16.64643832,17.15780683,17.62645046\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,14.40949887,15.23870272,15.98034255,16.64690635,17.24822997,17.79228819,18.28570284\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.62815892,16.34420761,16.97604444,17.53851754,18.04294486,18.49803075,18.91056589\n\"linker [O-]C(=O)CN(c1cc(cc(c1)C(=O)[O-])C(=O)[O-])CC(=O)[O-], n1ccc(cc1)c1ccncc1, nodes [Ni], [Ni][OH2][Ni], topology rna\",,,15.18487042,16.09304765,16.87351936,17.54900983,18.13753018,18.6534148,19.10816005\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.32944039,22.63440906,22.87271494,23.06226593,23.21540194,23.3408261,23.44480696\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.34629599,22.6487335,22.88501343,23.07292431,23.22471778,23.34903142,23.45208467\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.34391217,22.64677315,22.88337341,23.07153227,23.22352153,23.34799241,23.45117382\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.32956947,22.63450638,22.87279081,23.06232672,23.21545176,23.34086772,23.44484228\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.34421793,22.64697919,22.88351494,23.07163089,23.22359092,23.3480415,23.45120855\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.34336467,22.64631439,22.8829839,23.07119768,23.22323119,23.34773817,23.45094942\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.14340145,22.44649815,22.69081612,22.89010283,23.05445239,23.19136735,23.3064922\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.13006898,22.43498441,22.6807972,22.88132192,23.04670473,23.18448861,23.30034957\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,22.12987164,22.43468145,22.6804418,22.88094568,23.04632623,23.18411857,23.29999387\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.862679027,4.550073139,5.248745075,5.942746254,6.620317737,7.273504847,7.897514311\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.309357571,3.995198969,4.700511242,5.407302019,6.101941864,6.774923663,7.420241051\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.465117863,4.104137997,4.7659855,5.434331936,6.096204452,6.742083816,7.365562605\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.541135181,4.207678462,4.893271532,5.580767086,6.25712997,6.913198334,7.543112817\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.024024901,6.763805258,7.456812171,8.105100823,8.710275888,9.273803746,9.797246413\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.847411257,4.533922978,5.232180173,5.926136561,6.603937767,7.257547181,7.882106107\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.312379779,3.998483312,4.703950683,5.410809289,6.105449697,6.778382537,7.423616068\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.471125078,4.11050533,4.772529426,5.440905801,6.102698283,6.748419612,7.371688213\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.528824299,4.194600879,4.879817016,5.567249059,6.243783656,6.900190192,7.530553613\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.005462984,6.745708544,7.43932371,8.088298056,8.694197684,9.258464903,9.782645787\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.854969998,4.54205594,5.240619178,5.934662711,6.612385079,7.265797226,7.890079399\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.307065677,3.9929464,4.698339006,5.405233968,6.09998973,6.77309113,7.418526728\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.465531681,4.104662964,4.766582569,5.434969856,6.096859642,6.742739326,7.366206817\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.535797828,4.202178695,4.887770274,5.575378566,6.251929575,6.908231694,7.538403963\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.017829125,6.757742865,7.45094024,8.099453352,8.70487194,9.268652344,9.792349634\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.862586522,4.550017153,5.248719483,5.94274575,6.620337734,7.273541407,7.89756408\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.309446246,3.995311426,4.700644736,5.407453298,6.102107528,6.775100406,7.420425823\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.464814327,4.103810382,4.765641764,5.433979173,6.095848571,6.74172952,7.3652135\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.541343672,4.207936071,4.893563049,5.58108055,6.257456125,6.913530121,7.543444929\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.019232608,6.759221926,7.452472266,8.101015238,8.706442423,9.270213189,9.793886036\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.847201413,4.533756216,5.232048154,5.926032873,6.603857398,7.257486146,7.882061191\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.31219211,3.99827285,4.703723564,5.410571393,6.105206146,6.778137526,7.42337288\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.470845993,4.110221547,4.772241471,5.440615595,6.102408193,6.748131948,7.371405001\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.52965185,4.195490566,4.880747332,5.568201197,6.244742169,6.901142952,7.531491445\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.004099721,6.744258596,7.437809859,8.086741768,8.692618637,9.256880447,9.781070625\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.854787614,4.541870567,5.240438695,5.934492061,6.612227009,7.265652951,7.889949126\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.306834504,3.992746196,4.698170938,5.405096973,6.099881392,6.77300837,7.418466265\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.465571772,4.104692181,4.766604604,5.434987471,6.096874806,6.742753387,7.366220658\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,3.535868021,4.202249899,4.887840977,5.575447539,6.251995907,6.908294767,7.538463406\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.01690663,6.756865273,7.450119959,8.098694267,8.70417313,9.268010404,9.791760061\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.894443521,7.70647369,8.513570824,9.30984173,10.08970666,10.84810789,11.58075494\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.621106004,8.423460075,9.21324426,9.985801879,10.73708363,11.46358975,12.16244255\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.810305174,7.588880664,8.363161619,9.128029903,9.878822539,10.61125573,11.32154285\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.526705095,8.30615085,9.080217818,9.844394321,10.59364533,11.32307612,12.02840264\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.07203576,10.7917165,11.49480805,12.17699814,12.83449927,13.46436849,14.06458513\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.587360027,10.34442715,11.08048759,11.79185436,12.47527628,13.12828812,13.74928881\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.945386897,8.700419384,9.439449075,10.1622541,10.86746735,11.55295104,12.21629712\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.993465899,10.74276444,11.4657326,12.15962177,12.82273134,13.45405021,14.05310201\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.938570075,10.67797303,11.3971625,12.09233006,12.760273,13.39858343,14.00568379\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.634078048,8.410876605,9.183827375,9.947896575,10.69758307,11.42762158,12.13346214\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.912956901,7.710080648,8.498017397,9.271608345,10.02667768,10.75968263,11.46764408\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.890696456,7.702662459,8.509846186,9.306291118,10.08637547,10.8450145,11.57790105\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.6131012,8.415633795,9.205673199,9.97853839,10.73015872,11.45701776,12.15622563\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.810183909,7.588100135,8.36190705,9.12643632,9.876989936,10.6092592,11.31943935\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.531251183,8.309987825,9.083515752,9.847270251,10.59618169,11.32533259,12.03042369\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.06497449,10.78466261,11.48783805,12.17018209,12.82789242,13.45800985,14.0584991\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.579816877,10.33726099,11.07372414,11.78550263,12.46933189,13.12273733,13.74411205\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.942273156,8.697298136,9.436402199,10.15933893,10.86471967,11.55038971,12.2139286\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.981207891,10.73071172,11.45408686,12.14850122,12.81219515,13.44411816,14.0437689\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.931887264,10.67127379,11.39051792,12.08580686,12.75392504,13.39244981,13.99979013\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.63356967,8.410124084,9.182904741,9.946858792,10.69647037,11.42646332,12.13227987\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.908305119,7.705312747,8.493222894,9.26684977,10.02199902,10.7551148,11.46320849\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.895042777,7.707050973,8.51418797,9.310527823,10.09047061,10.84894683,11.58165975\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.609047566,8.411966662,9.202383172,9.975600342,10.72754069,11.45468603,12.15414754\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.806361546,7.584981631,8.359360892,9.124358489,9.87529648,10.60788161,11.31832144\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.528609088,8.30765915,9.081460807,9.845449534,10.59455969,11.32387896,12.02911322\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.07092746,10.79077198,11.49402746,12.17637661,12.83402717,13.46403289,14.06437135\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.580448618,10.33797802,11.07449575,11.78630414,12.47014436,13.12354675,13.74490833\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.941647602,8.696602526,9.435685493,10.1586306,10.86403657,11.54974074,12.21331778\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.982465492,10.73193795,11.45525361,12.14959496,12.81321155,13.4450583,14.04463673\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.935517911,10.6748679,11.39408072,12.08932832,12.75738981,13.39584236,14.00309703\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.634995949,8.411779752,9.184748833,9.948851681,10.69857504,11.42864637,12.134512\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.918524269,7.714840829,8.502150729,9.27524594,10.02991676,10.7625964,11.47028837\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.893808229,7.705753003,8.512803072,9.309053191,10.0889152,10.84732551,11.57998962\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.621436064,8.423847938,9.213677918,9.986270788,10.73757855,11.46410267,12.16296662\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.810947983,7.589352092,8.3635023,9.128270239,9.878985589,10.61135918,11.32160034\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.527365411,8.306832478,9.080961963,9.845216565,10.59454531,11.32404463,12.02942633\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.06987946,10.78968049,11.49288122,12.17517263,12.83276905,13.4627285,14.06303079\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.587987296,10.34504655,11.08109351,11.7924426,12.47584405,13.12883379,13.74981159\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.945297896,8.700404659,9.439496714,10.16235256,10.8676062,11.55312124,12.216491\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.993477232,10.74283582,11.46583465,12.15973502,12.82284339,13.45415364,14.05319277\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.937742032,10.67734057,11.39668164,12.09196731,12.7600027,13.39838575,14.00554332\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.635905051,8.412646501,9.185563002,9.949605799,10.69926522,11.42927187,12.13507447\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.915163126,7.712046546,8.499792381,9.273229921,10.02817402,10.76107478,11.46894772\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.888397345,7.700520734,8.507837854,9.304398384,10.08458527,10.84331717,11.57628926\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.614563883,8.417085901,9.207103334,9.979938994,10.73152468,11.45834556,12.15751288\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.809557929,7.587612317,8.361530723,9.126151002,9.876779244,10.60910971,11.31933994\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.530849887,8.309628502,9.083180797,9.846948161,10.59586575,11.32501945,12.03011217\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.06263072,10.78253404,11.48589215,12.16839422,12.82624327,13.45648383,14.05708326\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.579565833,10.33707253,11.07358769,11.78540909,12.46927358,13.12270781,13.74410594\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.941863171,8.696931774,9.436083439,10.15906706,10.86449158,11.5502012,12.21377512\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.980411877,10.73008322,11.45358017,12.14808338,12.81184244,13.44381362,14.0435004\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.933156996,10.67252979,11.39175717,12.0870259,12.7551204,13.39361831,14.00092901\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.632782952,8.409424506,9.182267562,9.946268683,10.69591796,11.42594291,12.1317879\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.909477667,7.706425583,8.49427559,9.267845976,10.02294338,10.75601168,11.4640616\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.894471416,7.70661448,8.513845298,9.310251317,10.09024158,10.84875257,11.58149151\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.608770922,8.411630342,9.201994944,9.975168807,10.72707456,11.45419362,12.15363644\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.806485559,7.585158684,8.359552505,9.124542135,9.875459976,10.6080193,11.31843168\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.525281013,8.304610213,9.078618367,9.842767315,10.59200911,11.32144278,12.02678107\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.07017378,10.79002412,11.49329211,12.17565844,12.83332934,13.46335745,14.06371949\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.580361224,10.33799234,11.07458812,11.78645566,12.47033998,13.12377447,13.74515861\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.941340681,8.696404498,9.435567561,10.15857131,10.86401984,11.5497545,12.21335298\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.983265377,10.73264706,11.45588957,12.15017165,12.81373957,13.44554568,14.04508953\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.936532069,10.67581028,11.39495559,12.09013954,12.75814118,13.39653776,14.00374037\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,7.633719984,8.410480707,9.18340906,9.947470227,10.69716009,11.42721016,12.13306771\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,6.919175691,7.715632612,8.503045452,9.276215109,10.03093791,10.76365142,11.47136254\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.953641179,10.86888809,11.74541189,12.57924807,13.36750642,14.10853921,14.80189375\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.774003141,10.68384358,11.55873336,12.39371956,13.1851544,13.93080372,14.62976021\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.00486342,10.91505874,11.78721702,12.617257,13.40219348,14.14030235,14.8310695\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.771029535,10.68135785,11.55671615,12.39212869,13.18393761,13.9299068,14.62913166\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.00113864,10.91103103,11.78298008,12.6128916,13.39776741,14.13587097,14.82667681\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.756091624,10.66813017,11.5449989,12.38173507,13.17469857,13.92167246,14.6217709\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.965020369,10.87964826,11.75560159,12.58890222,13.37665207,14.11719949,14.81009025\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.776315085,10.68613481,11.5610097,12.39597657,13.18738283,13.93299296,14.63190027\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,10.00076085,10.91092568,11.78309622,12.61318517,13.39820064,14.13641186,14.82729855\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.764706355,10.67579077,11.5517858,12.38773691,13.18000405,13.92636563,14.62592871\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.98593426,10.89684021,11.76969008,12.6004175,13.38604272,14.12484101,14.81629444\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,9.749733051,10.6623095,11.53963514,12.37676759,13.17008118,13.91736891,14.61775175\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.44899794,16.20149261,16.87203315,17.47318693,18.01471634,18.50437321,18.94844976\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.94968144,15.7834408,16.52157418,17.17893381,17.76719722,18.29572386,18.77215309\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.96829336,15.79319649,16.52916917,17.18830097,17.78043976,18.31375775,18.79515043\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,16.39375026,17.06064268,17.65459311,18.18610073,18.6634689,19.09341968,19.48153053\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.53715276,16.25090692,16.88511585,17.45303733,17.96493631,18.42881692,18.85099445\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.5035057,16.24864149,16.91317293,17.50936699,18.04676117,18.53293775,18.97405982\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.94949794,15.78294343,16.52089766,17.17816216,17.76638246,18.29489792,18.77133537\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.9634124,15.78893065,16.5254093,17.18495574,17.77743512,18.31103482,18.79266287\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,16.39853744,17.06428608,17.65737255,18.18822158,18.66508394,19.09464385,19.48245109\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.56067789,16.27095822,16.9023913,17.46806996,17.97813645,18.44050342,18.86141756\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.4822136,16.23049597,16.89759471,17.49590459,18.03505721,18.52270568,18.96506752\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.93567932,15.77099117,16.51044836,17.16893773,17.75816861,18.28752798,18.76467824\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.97947305,15.80383072,16.53928807,17.197924,17.78958223,18.32243432,18.80337673\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,16.40398678,17.06926379,17.66196169,18.19247784,18.66904666,19.09834255,19.48590923\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.59668311,16.30191621,16.92935355,17.49179907,17.99920081,18.45933749,18.878361\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.45965256,16.21107917,16.88071445,17.48109114,18.02194577,18.51101085,18.9545641\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.9505681,15.78417874,16.52222432,17.17953181,17.76776311,18.29626822,18.7726811\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.97862876,15.80293888,16.53834537,17.19694051,17.78857251,18.32141305,18.80235676\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,16.39631171,17.06272848,17.65630971,18.18752738,18.66466532,19.09443148,19.48239288\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.53731819,16.25108007,16.88534101,17.4533286,17.96529204,18.42922818,18.85144973\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.49756483,16.24342408,16.90853705,17.50521016,18.04300712,18.52952797,18.97094815\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.95402837,15.78687601,16.5243002,17.18110332,17.76892637,18.29710194,18.77324953\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.96658951,15.79224266,16.52873722,17.18822783,17.78060915,18.31408709,18.79558135\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,16.40945494,17.0733997,17.66507996,18.19481397,18.670779,19.09960727,19.48681104\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.55021346,16.26188863,16.8944556,17.46106652,17.97190791,18.43492572,18.85639185\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.470763,16.22040167,16.88860053,17.48781949,18.02773625,18.51603677,18.95896223\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.94012762,15.77484516,16.51378379,17.17182728,17.760678,18.28971462,18.76659129\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,14.97530537,15.79997982,16.53570967,17.19458788,17.78646639,18.31952143,18.80065208\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,16.39301403,17.06003843,17.65409903,18.18569814,18.66314177,19.09315443,19.48131573\n\"linker Oc1cccc(c1)C1=N[C](C(=N1)C(=O)[O-])C(=O)[O-], nodes [Mn], topology \",,,15.5935149,16.29896941,16.92655263,17.48910353,17.99659067,18.4568043,18.87590239\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,21.80093082,22.03473168,22.21911903,22.36687415,22.48695562,22.58577753,22.66802\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,21.80959466,22.04251126,22.2260609,22.37306313,22.49248326,22.59072982,22.67247323\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,21.80418218,22.03743863,22.22140532,22.36882941,22.48864611,22.58725314,22.66931897\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,21.80792539,22.04111049,22.2248709,22.37204095,22.4915965,22.5899537,22.67178856\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,21.68925083,21.94045522,22.13861689,22.29744192,22.42653833,22.53278748,22.62121259\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,21.70918883,21.95739415,22.15317597,22.31008313,22.43761262,22.54256588,22.62990754\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.493960391,4.172927833,4.869714857,5.567415628,6.253078661,6.917588899,7.555146575\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.45118279,4.099985664,4.769066965,5.442558211,6.108021489,6.756443087,7.381841981\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.504681578,4.184665561,4.882158443,5.580276762,6.266104598,6.930564314,7.567890493\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.447201223,4.095953489,4.765045407,5.438588037,6.104130268,6.752649448,7.37815817\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.4940951,4.173060447,4.869848338,5.5675509,6.253215597,6.917726897,7.555284883\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.450849519,4.099644064,4.768724741,5.442220535,6.107691789,6.756123571,7.381533987\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.504343566,4.184305965,4.881778874,5.579881208,6.265698403,6.930153464,7.567481144\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,3.447463539,4.096187801,4.765252106,5.438768711,6.104287209,6.752785269,7.378275538\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.622439763,8.486557927,9.338082282,10.16990986,10.97593727,11.75123909,12.49215506\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,8.006442331,8.842850118,9.669219433,10.47877277,11.26517692,12.02309639,12.74845623\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.533349134,10.36041311,11.15406729,11.91154892,12.63113988,13.3119744,13.95390331\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.807015868,8.634283416,9.450393517,10.24997393,11.02765339,11.77865376,12.49913818\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.519222722,8.355882842,9.180968585,9.988316965,10.77256294,11.52924137,12.25488178\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.770503365,10.55176997,11.30296381,12.0222603,12.70827271,13.36009307,13.97731201\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.230581866,8.056314471,8.86697392,9.657711797,10.42476446,11.16509287,11.87628147\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.641071107,8.484464151,9.312925146,10.11983015,10.9002548,11.650536,12.36805333\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,6.967338959,7.774972456,8.572312755,9.354114544,10.11614439,10.85484206,11.56725376\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.109556023,7.868852418,8.623657746,9.368956028,10.10033448,10.81381143,11.50588109\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.654411781,8.519418186,9.37122992,10.20288332,11.00839702,11.78294385,12.52293963\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,8.07198184,8.908234142,9.73355953,10.54146117,11.32581646,12.08144418,12.80438079\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.597164078,10.42235349,11.21361947,11.96839462,12.68512119,13.36305103,14.0021152\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.852498186,8.678182496,9.492342144,10.28976018,11.06519049,11.81394488,12.53224593\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.520190194,8.360732091,9.188947028,9.998780207,10.78496276,11.54311431,12.26983889\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.80943123,10.5906912,11.341311,12.05964144,12.74443318,13.39487965,14.01064395\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.289257338,8.105827212,8.909089902,9.693770401,10.45581574,11.19197795,11.89968282\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.702795806,8.55012755,9.380186978,10.18701256,10.96620277,11.7144899,12.42954343\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.001183614,7.804121906,8.597671878,9.376251619,10.13546569,10.87167446,11.58188107\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.105443069,7.868537708,8.626145222,9.373467398,10.10627414,10.82072921,11.51343939\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.620946198,8.485072249,9.33662158,10.16848224,10.97454674,11.74988789,12.49084459\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,8.005748641,8.842217477,9.668645772,10.47825273,11.26470416,12.02266471,12.74806008\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.534045692,10.36093238,11.15446306,11.91185719,12.63138508,13.31217335,13.95406777\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.806317388,8.633554669,9.449645027,10.24921302,11.02688593,11.77788484,12.49837233\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.519036696,8.355611355,9.180623069,9.987907404,10.77209885,11.528732,12.25433597\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.770642677,10.55180648,11.30291942,12.02215072,12.70811013,13.35988753,13.97707205\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.230274935,8.055586503,8.865976418,9.656546732,10.42350159,11.16378043,11.87495296\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.641342979,8.484598976,9.312964682,10.11980363,10.90018293,11.65043354,12.36793086\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,6.965919496,7.773756419,8.571264404,9.353203397,10.11534523,10.85413447,11.5666214\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.110273035,7.869406965,8.624076811,9.369263626,10.10055138,10.81395521,11.5059664\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.655066531,8.520150753,9.371997805,10.20365659,11.00915558,11.78367497,12.52363581\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,8.07217782,8.908423423,9.733724755,10.54159279,11.32591057,12.08150062,12.8044017\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.597006398,10.42221661,11.21349313,11.96827248,12.68499958,13.3629281,14.0019903\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.852759239,8.678438873,9.492580742,10.28997256,11.06537209,11.81409407,12.53236313\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.520750523,8.361216662,9.189353333,9.99910961,10.78521946,11.54330433,12.26996921\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,9.810529532,10.59165355,11.34215669,12.06038635,12.74509063,13.39546106,14.01115917\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.289865558,8.106260345,8.909382539,9.693949654,10.45590371,11.19199292,11.89964\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.702900948,8.55042595,9.380618171,10.18753183,10.96677742,11.71509622,12.43016439\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.00187061,7.804692902,8.598139789,9.376629062,10.13576483,10.87190668,11.58205674\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,7.105461979,7.868566133,8.626176407,9.373497173,10.1063,10.82074974,11.51345398\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.25078969,15.10366004,15.85911629,16.53264921,17.13661499,17.68088165,18.17338828\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.02930617,16.73508874,17.35864516,17.91530254,18.41602908,18.86891818,19.28015738\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.39170292,15.29468024,16.09453311,16.80635827,17.44239625,18.0126479,18.52539007\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.7893853,17.34774632,17.84749265,18.29964543,18.71213164,19.09070368,19.43961432\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.48313485,15.33427321,16.08856328,16.76094551,17.36341103,17.90561325,18.39539318\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.33588326,16.08296272,16.74876124,17.34588882,17.88422131,18.371581,18.81426478\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.05341042,16.70741547,17.29342735,17.82258651,18.30311189,18.74125853,19.14194367\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.88147219,15.6600445,16.35311352,16.97450428,17.53481774,18.0423316,18.50364288\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.86169395,17.9105336,18.78032459,19.50507,20.11253398,20.62497211,21.06008881\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.3546168,15.195015,15.94071699,16.60638779,17.20384761,17.74260961,18.2303725\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.37432407,17.04267655,17.63442508,18.16380873,18.64095844,19.07332142,19.46658066\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.74743841,15.61611718,16.3848921,17.06889892,17.68020546,18.22854473,18.72189509\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.1118197,16.76683905,17.34473428,17.86075561,18.32597992,18.74852468,19.13443449\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.43196229,16.17364151,16.83424468,17.42631989,17.95974507,18.44237005,18.8805235\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.33054304,16.07941433,16.74670272,17.34500649,17.88423455,18.3722565,18.81541658\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.39854887,16.13326406,16.78717379,17.37374349,17.90308499,18.38297839,18.81956647\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.20844061,15.95325928,16.61633416,17.21123516,17.74821985,18.23520583,18.67844622\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.70175298,17.77077377,18.65765407,19.39685714,20.01657817,20.53944689,20.98348122\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.22995924,15.08461759,15.84178136,16.51689572,17.12230082,17.66786431,18.16153271\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.16034036,16.84802207,17.4568194,18.00131741,18.49192818,18.93632516,19.34037562\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.40727913,15.30840406,16.10668616,16.81717588,17.45207368,18.02134696,18.53324514\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.79348754,17.35119594,17.85043372,18.30218335,18.71434488,19.09265166,19.44134278\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.46491883,15.31792017,16.07384116,16.74764723,17.35135631,17.89464709,18.38538292\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.3510162,16.09642414,16.76076443,17.35662457,17.8938565,18.38025971,18.8221105\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.05161038,16.70638919,17.292958,17.8225216,18.30334156,18.74170217,19.14254133\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.8787875,15.65761965,16.35092294,16.97252266,17.5330214,18.04069909,18.50215513\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.84165547,17.89286107,18.76469842,19.49120327,20.10017791,20.61391468,21.05015086\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.36618472,15.20557712,15.95038088,16.61524892,17.21199051,17.75010896,18.2372942\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.38953182,17.05602393,17.64621836,18.17429353,18.65033288,19.08174659,19.47418865\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,14.75317049,15.62155294,16.38998515,17.07363692,17.68459544,18.23260406,18.72564608\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.09641829,16.75363541,17.33328898,17.85073576,18.31713043,18.74064771,19.12737464\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.44069747,16.18138485,16.84114094,17.43248949,17.96528839,18.44737108,18.88505282\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.3194409,16.06984252,16.73839998,17.33776113,17.87787479,18.36664253,18.81043414\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.3847661,16.1210939,16.77635396,17.36406229,17.89437119,18.37509285,18.81239547\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,15.2233396,15.96651251,16.62817688,17.22186656,17.75780726,18.2438894,18.68634349\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [In], [O], topology sra\",,,16.67719131,17.74875987,18.63794636,19.37919754,20.0007198,20.52516568,20.9705793\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,21.50026678,21.86363765,22.14898149,22.37682975,22.56147373,22.71307515,22.83900266\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,21.49544539,21.85955903,22.1454935,22.37381726,22.55884858,22.71076903,22.83696198\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.25732014,3.859279045,4.490119262,5.134130387,5.77820375,6.412252841,7.02909849\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.701991953,4.39643011,5.106476307,5.814197896,6.506323361,7.173859162,7.811363359\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.782012948,4.477754175,5.184374367,5.885506567,6.569246688,7.227642275,7.855970773\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.32938211,3.92820064,4.554611417,5.193366505,5.83178585,6.460125309,7.071450964\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.869615394,3.324976365,3.820500481,4.347110315,4.89472311,5.453744289,6.015899591\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.856141837,3.311873612,3.807674777,4.334517444,4.882352945,5.441607332,6.004016847\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.261281663,3.863077141,4.493737955,5.137553239,5.781419406,6.415256377,7.031890813\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.693885982,4.388081351,5.098153066,5.806085021,6.498539057,7.166471808,7.804405921\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.783040961,4.478956762,5.185804638,5.887176492,6.571142318,7.229735229,7.85822623\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.332476825,3.931406366,4.557862503,5.196602775,5.834958984,6.463199883,7.074403096\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.877689947,3.332756526,3.828097693,4.354585196,4.902100381,5.461025786,6.023074218\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.865795416,3.321213409,3.816830937,4.343559166,4.891306051,5.450470058,6.012772064\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.255131454,3.856644559,4.487159338,5.130943985,5.774871007,6.408837713,7.02565129\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.697134469,4.391740392,5.102078952,5.810160479,6.502672532,7.170594243,7.8084668\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.780080393,4.475924793,5.182757289,5.884156037,6.568179667,7.226852179,7.855437454\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.333226637,3.932358625,4.558999654,5.197898292,5.836382654,6.464721382,7.075994165\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.877171904,3.331813101,3.826807915,4.353021754,4.900328224,5.459101397,6.021045554\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.870303754,3.325500016,3.82099581,4.347659651,4.895368931,5.454501884,6.016767122\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.250589933,3.85217657,4.482800401,5.126725531,5.770816967,6.404964013,7.021966729\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.705056055,4.399649248,5.109800799,5.817577687,6.509713166,7.1772208,7.814666301\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.779618335,4.475155261,5.181662922,5.882752916,6.566502829,7.224945389,7.853346485\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.331269113,3.930260811,4.556813543,5.195675949,5.834168856,6.462551199,7.073893094\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.866868592,3.32222815,3.817722553,4.344294451,4.891874605,5.450876306,6.013028945\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.860391876,3.316134977,3.812003436,4.338933026,4.886850163,5.446165801,6.008608543\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.256829876,3.858763879,4.489590693,5.133597918,5.777674843,6.411733079,7.028591836\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.701773815,4.396185721,5.106221738,5.813943981,6.50607708,7.173624762,7.811143214\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.781882881,4.477595719,5.184195903,5.885314955,6.569047394,7.227439547,7.855767838\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.329719303,3.928566768,4.554998452,5.193767138,5.832193774,6.460535293,7.0718588\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.870075957,3.325452046,3.820991961,4.347616145,4.895240398,5.454269464,6.016428995\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.856449636,3.312104253,3.807843865,4.334638932,4.8824387,5.441667203,6.004058922\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.260977866,3.862766224,4.493425619,5.137244664,5.781118728,6.414966595,7.031613899\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.694085705,4.388300308,5.098381034,5.806314514,6.498764864,7.166690486,7.804615346\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.783393043,4.479280845,5.186101841,5.887448685,6.571391639,7.229963828,7.858436154\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.332718217,3.931698954,4.558189543,5.196952348,5.835322335,6.463570426,7.074775808\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.878088506,3.333328434,3.828816608,4.355424963,4.90303608,5.462034719,6.024136539\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.866684819,3.322272752,3.818028429,4.344864904,4.89269274,5.451913663,6.014252159\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.25905882,3.860891503,4.491601734,5.135480131,5.779421112,6.41334144,7.030064584\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.693452429,4.388081085,5.098542554,5.8068122,6.499549258,7.167711941,7.805827064\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.779480204,4.47528303,5.182079346,5.883450301,6.567455416,7.226118316,7.854701855\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.334652831,3.933991086,4.560789844,5.199799554,5.838353589,6.466727201,7.078006801\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.878755074,3.333637099,3.828850351,4.355249287,4.902702465,5.461583196,6.023597777\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.867989358,3.322877664,3.818138364,4.344631688,4.89222666,5.451293058,6.013531268\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.255570259,3.85736197,4.488097283,5.132051157,5.776103027,6.410156878,7.027026048\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.700268004,4.394693204,5.104836821,5.812720154,6.505038458,7.172776004,7.810477132\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.778985778,4.474602132,5.181174366,5.882318142,6.566113733,7.224595641,7.85303096\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,3.332058739,3.931243362,4.557946256,5.19691742,5.835482506,6.463906577,7.07526592\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.868461568,3.324043653,3.819722459,4.346439102,4.894125547,5.453198164,6.015390475\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,2.857575013,3.313044118,3.8086883,4.335445353,4.883240224,5.442479714,6.004886671\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.42864553,10.14816997,10.85680413,11.54886751,12.21954854,12.86506027,13.48266255\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.897258684,10.61605193,11.31546405,11.99210621,12.6431658,13.26650058,13.86065506\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.731939977,8.489354018,9.235631399,9.968713627,10.68576792,11.38358616,12.05903461\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.02778714,10.7486545,11.45166082,12.13255202,12.78782548,13.41486269,14.01192508\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.483010182,10.19412242,10.89741086,11.58621003,12.25498913,12.89945048,13.51650087\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.235808723,10.09710009,10.93158352,11.7321363,12.49327876,13.21151505,13.88519932\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.434358659,10.15162416,10.8585328,11.54926979,12.21892925,12.86365596,13.48065894\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.905245164,10.62249043,11.32066129,11.99629691,12.64653423,13.26919402,13.86279277\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.735337642,8.490258926,9.234662654,9.966344366,10.68236511,11.37943586,12.05435966\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.0330684,10.75248815,11.45453453,12.1347943,12.78965609,13.4164273,14.01331911\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.479624317,10.19028243,10.89344705,11.58232081,12.25128911,12.89600073,13.51332836\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.244495341,10.10403025,10.9373203,11.73705516,12.49762582,13.2154501,13.88882562\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.432714893,10.1509046,10.85848666,11.54971108,12.2197193,12.86469105,13.48186144\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.89564401,10.61381467,11.31276477,11.98906675,12.63988199,13.26304906,13.85709751\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.745478517,8.499799567,9.243700301,9.974940796,10.69056101,11.3872593,12.06183125\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.03205237,10.75132859,11.45330145,12.13352942,12.78838499,13.41516617,14.01207846\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.479046956,10.18990607,10.89324878,11.58227615,12.25137408,12.89619299,13.51360781\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.252640475,10.11114253,10.94366876,11.74281974,12.50292686,13.22036888,13.89341827\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.429377401,10.14791717,10.85580062,11.54729954,12.21756409,12.86277641,13.48017139\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.899470011,10.61802211,11.31725189,11.99374996,12.6446905,13.26792308,13.86198729\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.734240502,8.490605563,9.236044141,9.968462129,10.68499701,11.38241523,12.05756123\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.03144709,10.75150824,11.45392834,12.13438954,12.78934402,13.41614143,14.01302081\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.480806626,10.1915724,10.89470584,11.58347123,12.25229262,12.89684279,13.514009\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.238371623,10.10001688,10.93473187,11.73541737,12.49661616,13.21485168,13.8884937\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.428701151,10.14817031,10.85676832,11.54880853,12.21947536,12.86497915,13.48257786\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.899416245,10.61798457,11.3172144,11.99370634,12.64463995,13.26786724,13.86192849\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.732026237,8.489365903,9.235587844,9.968628616,10.68565207,11.3834477,12.05887996\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.02811224,10.74889154,11.45182539,12.13265758,12.78788341,13.4148825,14.01191462\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.482542353,10.19368645,10.89700483,11.58583058,12.25463275,12.89911407,13.51618189\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.234100254,10.09509581,10.92937174,11.72979138,12.49086069,13.20907072,13.88276435\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.434748652,10.15207344,10.85902475,11.54979223,12.21947271,12.86421281,13.48122294\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.905019381,10.62235573,11.32060137,11.99629797,12.64658462,13.269284,13.86291419\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.735108829,8.490402812,9.235079498,9.966955228,10.68310821,11.38026366,12.05523629\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.03432807,10.75371006,11.45567687,12.13583616,12.79058984,13.41725351,14.01404313\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.477166677,10.18812179,10.89153192,11.58061322,12.24975945,12.89462497,13.51208652\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.244524507,10.10417082,10.93751847,11.73727704,12.497851,13.21566695,13.88902811\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.42377488,10.14256181,10.85066783,11.54235831,12.21278628,12.85814033,13.47566215\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.902453306,10.62014552,11.31864659,11.99453074,12.64495968,13.26777119,13.8614933\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.745215475,8.499229491,9.242913064,9.974004871,10.68952878,11.38617058,12.06071597\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.03016588,10.74948736,11.45152232,12.1318245,12.7867618,13.41362839,14.01062683\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.481874332,10.19276469,10.89608408,11.58504849,12.2540561,12.89876708,13.51606384\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.252204114,10.11075023,10.94329316,11.7424473,12.50255202,13.21999047,13.89303726\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.434200395,10.15229988,10.85980239,11.55096658,12.2209338,12.86588008,13.48303587\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.90930784,10.62674789,11.32501595,12.00068074,12.6508983,13.27350262,13.86701976\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,7.733171438,8.48953601,9.235009552,9.967484868,10.68408975,11.38158373,12.05680646\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.02525146,10.74584482,11.44873491,12.12961513,12.78494566,13.41208201,14.00926777\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.479785885,10.19078672,10.89407172,11.58292921,12.25180177,12.89637609,13.51354948\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,9.237665768,10.09927015,10.93393742,11.73457813,12.49574053,13.21395032,13.88757751\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.6802221,13.51039598,14.22496374,14.84502073,15.38889055,15.87176378,16.30583978\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.68172889,13.51173677,14.22616285,14.8460994,15.38986672,15.87265231,16.30665293\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.6772678,13.50738218,14.22205026,14.84229103,15.38638282,15.86948964,16.30379564\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.67683105,13.50694519,14.22164081,14.84192274,15.38606107,15.86921509,16.30356628\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,5.733869002,6.554811457,7.40233644,8.261848402,9.119209654,9.962156717,10.78092314\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,5.733210392,6.55403039,7.401448381,8.260872328,9.118165451,9.961063456,10.77979806\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,20.8401489,21.13861308,21.41086054,21.65798107,21.88134096,22.08260149,22.26360603\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,20.84037303,21.13881935,21.41105042,21.65815593,21.88150212,22.08275017,22.2637434\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,20.8489752,21.14667618,21.41821546,21.66468912,21.88746371,22.0881976,22.26872976\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,20.84880839,21.14663227,21.4182513,21.66477617,21.88758291,22.08833616,22.26887906\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.9006118,11.67840183,12.42859554,13.14820427,13.83455121,14.48566558,15.1004109\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.96888943,11.74125121,12.48661749,13.20189436,13.88432966,14.53189626,15.14341375\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.93978058,11.71396767,12.4610246,13.17787929,13.86179172,14.51074193,15.12355436\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.95059018,11.72482678,12.4717956,13.18845696,13.87209819,14.52072211,15.13317179\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.90502873,11.68224851,12.43195031,13.15113598,13.83711972,14.48792249,15.10240042\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.96606912,11.73864408,12.48422387,13.19970854,13.88234131,14.53009209,15.14177894\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.92610217,11.70172956,12.45000414,13.16789675,13.85270166,14.50242593,15.11591521\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,10.93732322,11.71268009,12.46063694,13.17817319,13.86259309,14.51191375,15.12498998\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,15.81422446,16.41747113,16.94752407,17.41679587,17.83551036,18.21212605,18.5535911\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,15.81241542,16.41586135,16.94608495,17.41550233,17.83434118,18.21106349,18.55262049\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,15.85271075,16.44992692,16.97513815,17.44048755,17.85599506,18.22996509,18.56922893\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,15.86128087,16.45711874,16.9812316,17.44569545,17.8604812,18.23385708,18.57262737\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.65659472,13.49585856,14.28053011,15.01188426,15.69112963,16.31986394,16.90017751\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.94805324,13.75839876,14.51813041,15.22776419,15.88795098,16.49986457,17.06526279\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,13.03840716,13.8393056,14.59098881,15.29368625,15.94784104,16.55447146,17.11521548\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.72827392,13.56057083,14.33911305,15.06505647,15.73951414,16.36400375,16.94054696\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.6618878,13.5005245,14.28465836,15.0155507,15.6943986,16.32279,16.90280692\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.89177554,13.70724809,14.47143351,15.18498285,15.84864209,16.46365473,17.03183177\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,13.07956431,13.8750422,14.62236911,15.3215038,15.9726986,16.57683559,17.13545395\n\"linker n1ccc(cc1)OCC(COc1ccncc1)(COc1ccncc1)COc1ccncc1, nodes [Fe], topology sql\",,,12.73028378,13.56245638,14.34084845,15.06663492,15.74094007,16.36528751,16.9417015\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,19.34385051,19.89535287,20.33154021,20.68158983,20.96626715,21.20058376,21.39556128\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,19.35133567,19.90221028,20.33774139,20.6871676,20.97127766,21.20508888,21.39962071\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,19.35641856,19.90619087,20.34094926,20.6898148,20.97350547,21.2069945,21.40127302\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,19.35109598,19.90168627,20.33707664,20.68644358,20.9705406,21.20436466,21.39892334\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.639419122,5.037028512,5.478910544,5.95402873,6.45088274,6.959067404,7.469993176\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.63711806,5.035537965,5.478122945,5.953838154,6.451190744,6.959785457,7.471043398\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.638355399,5.035386576,5.476787348,5.951511733,6.448051981,6.955995401,7.466744347\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.644747867,5.041419416,5.482712984,5.957473531,6.454117905,6.962184117,7.473044492\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.637763596,5.034812782,5.476228625,5.950966606,6.447519964,6.955476616,7.466239234\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.644787115,5.041321106,5.482514879,5.957204015,6.453798385,6.961830778,7.472669579\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.639933367,5.037459465,5.479278587,5.954348464,6.45116471,6.95931929,7.470220629\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.636993908,5.035421095,5.478015778,5.953742278,6.451106885,6.959713642,7.470983151\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.634495663,5.029624479,5.468259819,5.939824376,6.433157193,6.93807813,7.446128142\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.634589956,5.029703355,5.46832551,5.939878837,6.43320212,6.938114991,7.446158195\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.640272014,5.033576582,5.470891078,5.941500412,6.434143836,6.93856882,7.446263737\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,4.640434428,5.033747133,5.471063848,5.941671319,6.43431016,6.938728832,7.446416426\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.2258637,10.70506257,11.19798216,11.70315686,12.21628379,12.73191437,13.24453209\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.20331544,10.68834412,11.18528267,11.69315333,12.20803546,12.72476977,13.23805246\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.23203419,10.70935281,11.20100674,11.70536764,12.21800495,12.73337174,13.24587757\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.21826625,10.69842771,11.19178821,11.69702505,12.20996876,12.72527944,13.23752126\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.23306201,10.71024464,11.20178395,11.7060468,12.21859942,12.73389265,13.24633441\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.22016956,10.69992619,11.19297494,11.69796853,12.21072041,12.72587849,13.23799808\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.2266466,10.70572572,11.19854967,11.70364657,12.21670932,12.73228633,13.24485899\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.20356114,10.68854573,11.18546755,11.69333984,12.20823486,12.72498805,13.2382919\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.1827161,10.66422844,11.15899827,11.66574538,12.18028293,12.69723359,13.2111227\n\"linker [O-]C=O, nodes [Zn], topology pcu\",,,10.182412,10.66393934,11.15872862,11.6654981,12.18005952,12.69703434,13.21094704\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,19.47737887,19.94321055,20.31458486,20.61478661,20.86052081,21.0639644,21.23413171\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,19.40520863,19.88182485,20.2618681,20.56910607,20.82060841,21.02882682,21.20298345\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,4.762429328,5.491302659,6.19914388,6.879305686,7.527698938,8.142204904,8.722244476\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.760119618,4.479159902,5.205769104,5.92353816,6.620718494,7.28963269,7.925893949\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.489748654,4.188728096,4.897545866,5.60077031,6.287093969,6.948868648,7.58146295\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,4.445439396,5.178980777,5.897479834,6.592119443,7.257128037,7.889128358,8.486628739\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.506878302,4.230365064,4.966069818,5.695808841,6.406550645,7.089713367,7.740283401\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.896027694,4.666029552,5.429872554,6.173126305,6.886297466,7.563788281,8.202954057\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.653832461,4.401203929,5.152306839,5.890645675,6.60479013,7.287505859,7.934844431\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.691893135,4.402608167,5.126153875,5.844558784,6.544834169,7.218362457,7.860064043\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,4.151869247,4.908509937,5.662657063,6.398563471,7.105731785,7.777909491,8.412082303\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,4.775681736,5.504215622,6.211493806,6.890974269,7.538637487,8.152408667,8.731735093\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.762072056,4.481743544,5.208859092,5.927025723,6.624507731,7.293639624,7.930046184\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.489947169,4.189340877,4.898623148,5.602316202,6.2890802,6.951247248,7.584176257\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,4.44497534,5.178325741,5.896649514,6.591140877,7.25603138,7.887942657,8.485379946\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.507083709,4.23050063,4.966151448,5.695852376,6.406569236,7.089716891,7.740278743\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.899149175,4.669344388,5.433292884,6.17658365,6.889739554,7.567176148,8.206259467\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.656896058,4.404007349,5.154855896,5.892953734,6.606875134,7.289387858,7.936543837\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,3.694631225,4.404864483,5.128013754,5.846092081,6.546097773,7.219402693,7.860918721\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,4.152590627,4.908955548,5.662820589,6.398459025,7.105385713,7.777354012,8.411351124\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,7.262433004,8.121956105,8.957991685,9.767599849,10.54829128,11.29787369,12.01453978\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.943120416,10.73262662,11.4924767,12.21942829,12.91108455,13.56595839,14.18342472\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,7.246915749,8.09581967,8.924717026,9.729262655,10.50618577,11.25287642,11.96730743\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.475235447,10.25952384,11.01649181,11.74300231,12.43661661,13.09570099,13.71941048\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,7.744034467,8.56274357,9.365171177,10.1483466,10.90866609,11.64251412,12.34674315\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.920475374,9.773039597,10.59076209,11.37094338,12.11171008,12.81204978,13.47174684\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.120233245,9.853850894,10.57455416,11.27836488,11.96098727,12.61853773,13.24793909\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.167384383,9.922100376,10.6614205,11.38063331,12.07518977,12.74132429,13.37630295\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.104962211,9.893817581,10.65622026,11.39031967,12.09390994,12.76502183,13.40224309\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.780895398,9.52315859,10.2545173,10.97042027,11.66600484,12.33691665,12.97972\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.355937511,10.05133524,10.74469682,11.428792,12.09684317,12.74321503,13.36365434\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.488677195,10.20886303,10.91784272,11.61031198,12.28125999,12.92654283,13.54310265\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,6.83464732,7.689111926,8.531788835,9.356359756,10.15747421,10.93067279,11.67244341\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,7.286248565,8.144714338,8.97974607,9.788425965,10.56826227,11.31705099,12.03297175\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.947407679,10.73706297,11.497049,12.22411615,12.91586197,13.57079619,14.18829291\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,7.253535525,8.102372776,8.931224861,9.735741252,10.51264081,11.25930349,11.97369453\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.462182625,10.24872177,11.0074241,11.73529358,12.42998854,13.08994388,13.71436413\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,7.730341551,8.551288292,9.355684165,10.14059493,10.90243983,11.6376207,12.34300577\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.936453283,9.789332663,10.60728802,11.38761461,12.1284358,12.82874011,13.48831698\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.110933476,9.846208045,10.56832268,11.27334766,11.95701601,12.61546447,13.24563265\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.16983758,9.924057954,10.66288365,11.3816418,12.07580067,12.74159935,13.37630158\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.102632849,9.891709461,10.65422839,11.38838641,12.09200674,12.76313735,13.40037572\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.788937593,9.529924204,10.26020775,10.97521258,11.67005057,12.34034332,12.98263362\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.370896842,10.06458102,10.75642502,11.43917637,12.10603943,12.75136314,13.37087982\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,9.490259307,10.21027245,10.91903716,11.61127363,12.28198863,12.92704993,13.54340673\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,6.82712698,7.686323394,8.532533826,9.359721934,10.16274847,10.93731589,11.68003755\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.488571366,9.268737367,10.03369441,10.78133195,11.50816231,12.21040493,12.88468653\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,10.07483434,10.8793028,11.66357086,12.42169127,13.14843175,13.83985223,14.49343302\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.570694784,9.303248979,10.03036691,10.74824059,11.45194876,12.13651044,12.79754778\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,10.08195536,10.84965366,11.60460365,12.33973874,13.04883893,13.72709161,14.37120836\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.461690896,9.244224745,10.01139665,10.76107667,11.48977109,12.19370223,12.86950525\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,10.06347037,10.86957015,11.65520014,12.41446464,13.14217081,13.83440952,14.48868585\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,8.584532944,9.316295082,10.0427049,10.75993406,11.46304576,12.14704841,12.80755742\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,10.0739227,10.84180436,11.59695611,12.3323157,13.04166222,13.72017899,14.36457222\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,14.22645965,15.09759686,15.87183352,16.56239649,17.18034429,17.7349345,18.23396574\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,14.76678164,15.56223393,16.27275455,16.91015022,17.4838421,18.00153771,18.46968824\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,14.24739714,15.11444407,15.88537119,16.57327019,17.18908105,17.74196021,18.23962204\n\"linker [O-]C(=O)c1cc(cc(c1)n1cncc1)n1cncc1, nodes [Co], topology pcu\",,,14.38845557,15.2272449,15.97408231,16.64220128,17.24212451,17.78240807,18.27016005\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,20.83232496,21.26963916,21.61825629,21.90001379,22.13059514,22.32144084,22.48102384\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,20.81477695,21.25884481,21.61172342,21.89622428,22.12859871,22.32062856,22.4809976\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,20.52934973,21.01582172,21.40270562,21.71479235,21.96979392,22.18057712,22.35663925\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,20.7565954,21.2093044,21.5691337,21.85928115,22.09628914,22.29215858,22.45573887\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.37711451,2.974371295,3.615046441,4.279741699,4.952097152,5.619377006,6.27235161\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.519918898,4.122493242,4.749903819,5.387340459,6.022622305,6.646489633,7.25243622\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.741787333,3.349259014,3.989850131,4.646767286,5.306032503,5.956872278,6.59156643\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.004119383,3.618671389,4.261956999,4.91835161,5.574725271,6.22093768,6.849756892\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.159617041,3.857645011,4.571914017,5.285510925,5.985636177,6.663351261,7.313006872\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.516991754,4.192016792,4.882446392,5.57257789,6.250348633,6.907227101,7.537750323\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.368206342,2.965701912,3.606661108,4.271669453,4.944354116,5.611968357,6.265273263\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.509623072,4.113348068,4.741813128,5.380209494,6.016357416,6.640999881,7.247635314\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.756293772,3.361565496,4.000066861,4.655068497,5.312625174,5.961972971,6.595385936\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.025132273,3.639496349,4.282365711,4.9381551,5.593784731,6.239162732,6.867098215\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.164725879,3.862474366,4.5763313,5.289444168,5.989060628,6.666275173,7.315459366\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.516620152,4.191408359,4.881687795,5.571723897,6.249434726,6.90627675,7.536779269\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.380346919,2.977116459,3.617232863,4.281346521,4.953143184,5.619924361,6.272487705\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.527037708,4.129932545,4.757505787,5.394983568,6.030214762,6.653964116,7.259745505\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.7442457,3.351788886,3.992422398,4.649348132,5.308590621,5.959381951,6.594008231\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.014567087,3.629794263,4.273569438,4.930269421,5.586781496,6.232989919,6.86168915\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.160293552,3.858307424,4.572535439,5.286074882,5.986134446,6.663781551,7.313370822\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.518036281,4.193041386,4.883457993,5.573577896,6.251335299,6.908197189,7.538700132\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.375660028,2.972383361,3.612536091,4.276753509,4.948703099,5.615668546,6.268432024\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.518431283,4.121796426,4.749762478,5.387590528,6.023149237,6.6472134,7.253301118\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,2.760980576,3.366849399,4.005800963,4.661108312,5.31884207,5.968259552,6.601656611\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.031190597,3.645856616,4.288927591,4.944825377,5.60048191,6.24581884,6.873658745\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.164881358,3.862543198,4.576337953,5.289406089,5.988990009,6.666180518,7.315346678\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,3.515481818,4.190022019,4.880146713,5.570099116,6.247778574,6.904626618,7.535161041\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.000719288,7.813792512,8.613186132,9.393967883,10.15236548,10.88538065,11.59064595\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.51026177,8.317173731,9.117509711,9.906140196,10.67737816,11.42586203,12.14708338\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.563363799,10.3466452,11.10098066,11.82496869,12.51701792,13.175791,13.80043353\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.597573912,10.30382023,10.99647647,11.67186605,12.32634537,12.95677213,13.56072194\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.617306576,8.486336549,9.348625279,10.19469622,11.01634139,11.80705061,12.5621157\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.845539706,7.649261813,8.446241517,9.229586468,9.994007352,10.73533575,11.45030763\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.227983172,10.03358022,10.80761951,11.54945437,12.25795216,12.93204519,13.57103791\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,8.843701867,9.679758238,10.47998945,11.24465457,11.97337911,12.66567008,13.32124391\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.299176271,8.120090073,8.920734905,9.700183379,10.45668805,11.18803554,11.89197748\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.349108369,8.161391727,8.949139188,9.713001152,10.45276776,11.16745956,11.85569689\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.935061659,7.748188917,8.549644616,9.335421844,10.10149895,10.84414071,11.56014928\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.413412346,10.28314662,11.10020851,11.86753536,12.58794996,13.26399205,13.89795346\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.440475883,10.25681639,11.03005506,11.76187219,12.45396315,13.10785492,13.7249273\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.980799388,7.793887676,8.593226177,9.373915218,10.13222748,10.86520251,11.57049739\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.485558927,8.292146614,9.091863742,9.879786634,10.65036875,11.39833293,12.11921238\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.540077954,10.32614553,11.08302617,11.80926712,12.50327671,13.16374015,13.78983385\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.577774373,10.28666004,10.98159094,11.65894506,12.31512288,12.94701855,13.55223852\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.598579839,8.471066339,9.335970202,10.1840593,11.00728835,11.79925886,12.55534148\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.805864132,7.618463539,8.422591181,9.211672895,9.980684835,10.72567815,11.44356876\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.248326532,10.04796105,10.81743417,11.55576391,12.26156617,12.93358484,13.57098263\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,8.86557232,9.697505911,10.49479835,11.25737189,11.98460072,12.67580938,13.33058451\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.320387199,8.138885532,8.937747131,9.715891919,10.47144016,11.20207246,11.90546025\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.363489454,8.173395937,8.959138655,9.72130387,10.45963222,11.17310467,11.86030903\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.938539822,7.749652964,8.549644828,9.334361391,10.0996744,10.8417717,11.55739962\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.401095755,10.2710008,11.08858231,11.85660451,12.57778453,13.25459973,13.88930675\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.440380024,10.25564709,11.02821967,11.75963421,12.45149503,13.10527063,13.72230262\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.001152663,7.814230843,8.612767052,9.392181928,10.14897544,10.88034199,11.58403947\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.510627622,8.316732687,9.116138659,9.903815896,10.67414773,11.42181628,12.14233562\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.587841531,10.36866736,11.12085965,11.84297565,12.53338771,13.19072677,13.81411097\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.600326432,10.30683756,10.99957929,11.67493327,12.32929992,12.95956894,13.56333845\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.614799279,8.484045721,9.346183598,10.19191569,11.01314689,11.80343598,12.55811444\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.810824523,7.623931398,8.428225451,9.217270503,9.986120598,10.73087434,11.4484789\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.237786287,10.04238689,10.81565184,11.55686803,12.26485674,12.9385186,13.5771364\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,8.84108925,9.676055612,10.47555945,11.23976153,11.96821548,12.66037575,13.31592024\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.295121841,8.116260931,8.917157031,9.696860671,10.45361179,11.18519052,11.88934579\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.332277715,8.144920228,8.933144044,9.697549705,10.43789586,11.15318305,11.84201864\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.93395547,7.747240802,8.548822078,9.334700203,10.10085937,10.84356869,11.55963353\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.411780153,10.28166999,11.09887893,11.86633733,12.58686614,13.26300586,13.89705024\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.444646002,10.26071453,11.03371888,11.76533076,12.45723864,13.11096429,13.72788376\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.018069123,7.822617879,8.614527073,9.388922504,10.1420057,10.87070104,11.57253682\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.500223128,8.303985733,9.101521551,9.887730167,10.65694482,11.40380513,12.12378526\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.572153289,10.35482369,11.10861396,11.83211114,12.52371688,13.18208872,13.80636809\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.563076337,10.27255263,10.9679998,11.64582459,12.30244712,12.93477386,13.54041821\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.611234448,8.48164916,9.344812079,10.1914156,11.01337031,11.80424812,12.55939664\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.806834698,7.621743687,8.427790892,9.218438215,9.988692207,10.73463718,11.45322538\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.257441078,10.05661845,10.82565588,11.56358176,12.26901279,12.94068954,13.57777022\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,8.85931573,9.690937263,10.48803906,11.25052391,11.97774641,12.66901366,13.32389745\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.312535258,8.131403553,8.930660644,9.709197463,10.46512009,11.19610348,11.89981792\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,7.360138371,8.169747611,8.955354494,9.717495818,10.45587648,11.1694517,11.85679075\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,6.942262866,7.753222979,8.553039452,9.337572375,10.10270192,10.8446208,11.56007801\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.415098729,10.2838879,11.10041736,11.86746546,12.58775288,13.26375529,13.89772505\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.451009993,10.26529294,11.03705128,11.76778173,12.45905844,13.11232715,13.72891254\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.719340953,10.59071786,11.41840257,12.2030189,12.94507787,13.64510308,14.30377498\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,11.42318126,12.22651177,12.97960779,13.68628768,14.34949206,14.97153141,15.55434925\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.702457051,10.64724297,11.53192433,12.35952985,13.13303969,13.85523513,14.5287393\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.713856515,10.58667805,11.41554897,12.20110168,12.94387846,13.64444099,14.30350669\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,11.40475532,12.20971816,12.96426937,13.67225376,14.33663073,14.95972574,15.54349495\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.781369479,10.71906221,11.5973405,12.41921346,13.18761018,13.90524953,14.57469131\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.728540433,10.60007335,11.42802411,12.21292258,12.95522543,13.65542878,14.31420289\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,11.43000066,12.2313219,12.98289724,13.68842452,14.35075422,14.9721298,15.55444477\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.749518468,10.68997217,11.57069619,12.39474311,13.16507933,13.88445517,14.55545687\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.71417552,10.58714778,11.41636582,12.20235534,12.94559119,13.64659379,14.306057\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,11.4025116,12.20651111,12.96059807,13.66843607,14.33286354,14.95612543,15.54012489\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,9.765783926,10.70641347,11.58715244,12.41104879,13.18109041,13.90005805,14.57056857\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.14120008,15.02146138,15.80986918,16.51791703,17.15528234,17.73017016,18.24961297\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.58935969,15.41184368,16.13182937,16.7680489,17.33498679,17.84386143,18.30341348\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,13.98281426,14.8842433,15.68349809,16.39560369,17.03289443,17.60547752,18.12168091\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,15.49113468,16.19813452,16.82428726,17.38444364,17.88957854,18.34791479,18.76573503\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,13.64557035,14.57350855,15.40444781,16.15024353,16.82103559,17.4255133,17.9711731\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.92536002,15.71434425,16.40518788,17.01599564,17.56069795,18.05003944,18.49236176\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.5121746,15.36354991,16.11771597,16.78960945,17.39120397,17.93214954,18.42030531\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.54917412,15.36944471,16.09075378,16.73121701,17.30453332,17.82113707,18.28908518\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,13.14664902,14.13072992,15.00885622,15.79466345,16.49968802,17.13370272,17.70504535\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,15.23223109,15.98209163,16.64060108,17.22445914,17.74650878,18.21665237,18.64257663\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.10971496,14.99528762,15.77993541,16.47904412,17.10500418,17.66782792,18.17568351\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,15.06679627,15.83157547,16.50434216,17.10255526,17.63913607,18.12375851,18.56379184\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,13.70063107,14.63741036,15.4725832,16.21968463,16.88994308,17.49275402,18.03607366\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,15.23374057,15.98429537,16.64277428,17.22626499,17.74781699,18.21743976,18.64287297\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.74511645,15.5681158,16.29686738,16.94647148,17.52875065,18.05306617,18.52694598\n\"linker [O-]C(=O)c1nccnc1C(=O)[O-], n1cc2ccc3c4c2c(c1)ccc4cnc3, nodes [Cu], topology pcu,\",,,14.53065165,15.35246937,16.07464195,16.71563913,17.28934974,17.80630548,18.27460935\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,20.77124789,21.14134319,21.44101119,21.68648183,21.88969311,22.05955436,22.20280266\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,20.6521107,21.04082403,21.35517273,21.61239813,21.82515162,22.00285516,22.15262056\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,20.5618526,20.999716,21.34516882,21.62200766,21.84697958,22.03209797,22.1861359\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,20.72019671,21.10578066,21.41657615,21.66998237,21.87883684,22.05270797,22.19880479\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.238135933,3.908416523,4.602978593,5.303477247,5.995476213,6.668557681,7.315879255\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.227760329,3.876777779,4.548516443,5.22645458,5.897584458,6.55242762,7.18464023\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.272908149,3.915306115,4.582379061,5.257215317,5.926363682,6.579938301,7.211261409\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.481473426,4.144723208,4.827746889,5.513885165,6.190170575,6.847312871,7.479257924\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.212377162,3.85670043,4.527463515,5.207174252,5.881840936,6.541152687,7.178136451\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.389768908,4.047183804,4.728100488,5.414911679,6.093780148,6.754704836,7.391090515\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.240301673,3.909787146,4.603562257,5.303355353,5.994779864,6.66744996,7.314542582\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.226369196,3.875274718,4.546887924,5.224705485,5.895730987,6.550491541,7.182644882\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.266395259,3.907878981,4.574196698,5.248451518,5.91718853,6.570506586,7.201706851\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.480157635,4.143025617,4.825664269,5.511448581,6.187432747,6.844337164,7.476110368\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.216984612,3.861342302,4.532019302,5.211569367,5.886033399,6.545122616,7.18187839\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,3.389223576,4.046524075,4.727299117,5.413972808,6.092734893,6.753606177,7.390008268\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,8.026772333,8.800773533,9.56253717,10.30935415,11.03767055,11.74379224,12.42439373\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.88325749,8.661699215,9.431038192,10.18706092,10.92521223,11.64116483,12.33121392\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.082814765,9.890436517,10.66994965,11.41811597,12.13253898,12.8116574,13.45468543\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.332885983,10.14745586,10.92992867,11.67796185,12.38984864,13.06458524,13.70184536\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.645385512,8.451276061,9.242352098,10.0157654,10.76803403,11.4956465,12.19550768\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.27931262,8.127158457,8.961887085,9.777195429,10.56782584,11.32953585,12.05911047\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.23300774,8.064592356,8.887703705,9.695317423,10.48136777,11.24086924,11.9699851\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.632614333,8.429352777,9.217756029,9.9929906,10.74988953,11.48364869,12.19025215\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.661755249,10.45135989,11.20604188,11.925512,12.60957843,13.25819711,13.87155451\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.53828324,10.32833552,11.08568419,11.80901962,12.49755449,13.1509043,13.76906294\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.519968164,10.30698988,11.06445038,11.79018445,12.48252287,13.14035882,13.76316537\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.638541479,10.40401164,11.14208235,11.85092916,12.5288785,13.17464085,13.78742922\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.69528107,7.50743298,8.311825397,9.102178817,9.873510157,10.6217141,11.34345171\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.661922951,7.435679869,8.210597309,8.979231265,9.735213279,10.47313199,11.18852891\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.869852711,7.616459736,8.366088914,9.111978941,9.848114433,10.56913511,11.27041785\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.673619336,7.465939207,8.255120369,9.034306962,9.797841589,10.54097006,11.25977886\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.026401894,7.894024768,8.744111262,9.569155661,10.36423153,11.12616383,11.85301646\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,8.035695164,8.808565289,9.569141907,10.3148111,11.04207381,11.74726155,12.42705549\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.881153238,8.659629341,9.428978698,10.18500622,10.9231678,11.63914132,12.32922336\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.087279331,9.894127633,10.67301989,11.42068799,12.13471421,12.81352053,13.45630745\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.329688617,10.14486425,10.92780657,11.67620626,12.38838256,13.06335093,13.70079909\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.653479945,8.45881317,9.249467544,10.02253974,10.7745152,11.50186311,12.20147715\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.28552144,8.132802037,8.967029876,9.781891442,10.57212391,11.33348058,12.06274208\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.241879495,8.071128468,8.89226818,9.698212646,10.48285771,11.24118779,11.96933882\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.637769306,8.434472878,9.222853765,9.998057587,10.75490925,11.48860253,12.19512225\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.665969551,10.45527399,11.20957644,11.92862898,12.61227257,13.26048541,13.87346724\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.532956685,10.32312709,11.08065838,11.80421357,12.49298868,13.14658812,13.76499802\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.520332434,10.3076782,11.06522775,11.79091097,12.4831226,13.14079693,13.76343241\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,9.636036801,10.4019338,11.14033416,11.84943622,12.52758677,13.17351245,13.7864384\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.707739464,7.518717039,8.322093478,9.111569289,9.88214351,10.62969349,11.35086395\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.685084809,7.456503967,8.22940509,8.996275964,9.750705343,10.48725143,11.20143178\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.873737388,7.619377686,8.368178882,9.113379716,9.848951652,10.5695172,11.27043602\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,6.678234526,7.469441253,8.257824378,9.036437,9.79955759,10.54238635,11.26097712\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,7.031370632,7.899176021,8.749291639,9.574257028,10.36918081,11.13091438,11.85754111\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,14.94784719,15.69214693,16.35703547,16.95410828,17.49289484,17.98116132,18.42524173\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.65317633,16.32204078,16.9152514,17.44660034,17.92635962,18.36228198,18.76031442\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,14.77253312,15.5559978,16.26671609,16.91096163,17.49490527,18.02436381,18.5047017\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,14.29515884,15.17709918,15.9641463,16.66863073,17.30074127,17.86906376,18.38095065\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.26258689,15.9778301,16.62419685,17.20990738,17.74186683,18.22592824,18.66710789\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.2952484,16.01163688,16.64948378,17.22181345,17.73852305,18.20727993,18.63414516\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.81795258,16.48013648,17.07655997,17.61668659,18.10776164,18.5555153,18.96462266\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,14.69065195,15.46194164,16.16539968,16.8058739,17.38850072,17.91835719,18.40028012\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,16.04503916,16.69653287,17.26444011,17.76515781,18.21150979,18.61332348,18.97805559\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.00991095,15.74741642,16.40655624,16.99873349,17.53332297,18.01796633,18.45889755\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.86544469,16.5090441,17.08097472,17.59429763,18.05869252,18.48143684,18.8680971\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,14.8100111,15.58715173,16.29310991,16.93367101,17.51469312,18.04178692,18.52017719\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,14.18878467,15.08152899,15.8784168,16.59169486,17.23158195,17.8067454,18.32463766\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.56928806,16.25044335,16.86678272,17.42626167,17.93539618,18.39961986,18.82354649\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.40763325,16.10828589,16.73340993,17.29531883,17.80339385,18.26492177,18.68567839\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,15.85967531,16.51889962,17.11239612,17.6497487,18.13825313,18.58365348,18.99062027\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,14.7175103,15.48595375,16.18704644,16.82551211,17.40640627,17.93475057,18.41534202\n\"linker O=C(c1ccc(c(c1)C(=O)[O-])C(=O)[O-])c1ccc(c(c1)C(=O)[O-])C(=O)[O-], nodes [Co], topology rna\",,,16.06114768,16.71107385,17.2776154,17.77714225,18.22245215,18.62334971,18.98727243\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,20.02284179,20.46118445,20.80914031,21.0893271,21.31789936,21.50657625,21.66399078\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,20.10030883,20.52685094,20.86541953,21.1380389,21.36043534,21.54401492,21.69717872\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,20.18626934,20.60447603,20.93525153,21.20086838,21.41707827,21.59522802,21.74363316\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.364339406,3.983245838,4.626485531,5.278735543,5.92752981,6.563495859,7.180131816\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.106533218,3.736071529,4.396281146,5.06903419,5.739678114,6.397289438,7.034357633\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.458105036,4.081930927,4.728136569,5.381656196,6.03027504,6.66485091,7.279084394\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.404643696,4.062782277,4.741201367,5.423641359,6.097295042,6.752882003,7.384270931\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.364612451,3.983569398,4.626846222,5.279120219,5.927927234,6.56389711,7.18053015\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.106136955,3.735637342,4.395818659,5.068552541,5.73918545,6.396792715,7.033862588\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.457056075,4.081035362,4.727393474,5.381058996,6.029813028,6.664510902,7.278852144\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,3.404217902,4.06234718,4.740767449,5.423217585,6.096889676,6.75250334,7.383927762\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.137399665,7.836430487,8.539847487,9.243669044,9.942908514,10.63227595,11.30675457\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.11869519,7.896741945,8.668931615,9.430438928,10.17642168,10.90235298,11.60431891\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.271094847,10.01622951,10.74512871,11.45327195,12.13660569,12.79188664,13.41680437\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.324123792,10.05341811,10.77022174,11.47015835,12.14860161,12.80152859,13.4258833\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,8.92647558,9.68206836,10.42395022,11.14673952,11.84557801,12.51659108,13.1570207\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.069290699,7.916349523,8.754120722,9.574902093,10.37238184,11.14156789,11.87873862\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.443741271,8.244753474,9.036076296,9.81291863,10.570446,11.30424324,12.01063128\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.191891897,10.01829554,10.80935683,11.56336169,12.27926442,12.9566241,13.59554807\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,6.681625927,7.475149222,8.266697657,9.047570753,9.811081219,10.55212026,11.26686878\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,6.663122589,7.430342859,8.19716156,8.957419518,9.705534604,10.43649172,11.14596389\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.137718269,7.836500442,8.539752517,9.243465848,9.942635958,10.63196088,11.30641561\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.120766221,7.89859657,8.670632925,9.432033945,10.17794375,10.90382451,11.60575406\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.271378255,10.01623704,10.74494934,11.45296678,12.13621748,12.79144567,13.41633224\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.32333666,10.05262129,10.76941621,11.46934997,12.14779769,12.8007361,13.42510811\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,8.919148369,9.675435781,10.41794383,11.14129609,11.84063954,12.51210475,13.15293874\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.069414663,7.916379018,8.75402966,9.57468634,10.37204945,11.14113295,11.87821754\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,7.446767913,8.247559474,9.038681686,9.815339528,10.5726962,11.30633518,12.01257655\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.194083389,10.02053132,10.81159157,11.56556479,12.28141562,12.95871047,13.59756198\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,6.680376703,7.474081601,8.265747858,9.046691252,9.810239528,10.55129597,11.26605033\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,6.663136372,7.430327686,8.197132657,8.95738812,9.705508383,10.43647544,11.14596011\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.875262654,10.65649723,11.42883709,12.18417307,12.91501297,13.61538065,14.28108032\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.06898695,10.85934078,11.64403585,12.41256098,13.15572909,13.8665352,14.54027942\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.62642963,11.3940889,12.15584688,12.90103356,13.62059648,14.30780026,14.95824354\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.59323187,11.37998518,12.15073663,12.89798623,13.61523973,14.29766373,14.94218382\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.26823916,11.11557285,11.92147255,12.68580266,13.40827294,14.08880635,14.72773146\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.40808668,11.2668161,12.07745621,12.84156692,13.56039535,14.23509897,14.86692727\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,9.884662991,10.66502936,11.43659801,12.19125018,12.92148374,13.62131303,14.28653359\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.07859159,10.86884813,11.65332624,12.42155744,13.16438384,13.87482096,14.54818351\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.59875719,11.36897457,12.13296485,12.8801161,13.60141912,14.29017196,14.94199987\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.59464716,11.38122297,12.15178699,12.89885686,13.61594698,14.29822732,14.94262384\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.29946991,11.14397282,11.94739353,12.70954125,13.43007998,14.10889534,14.74628541\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,10.40921635,11.26778924,12.07825476,12.842191,13.56085563,14.23541155,14.86711044\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,16.63963897,17.15457072,17.61756901,18.03755595,18.42138754,18.77432311,19.10040113\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,14.58524178,15.47008222,16.25227864,16.94691036,17.56602542,18.1194719,18.61546535\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,14.60594341,15.4207365,16.14928043,16.80333754,17.39232647,17.92399508,18.4048651\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,15.05147063,15.79086161,16.4479799,17.03624604,17.56604451,18.04550956,18.48111237\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,16.64322091,17.15760427,17.62021988,18.03992428,18.42353687,18.77629565,19.10222617\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,14.56308767,15.44970781,16.23351497,16.92959963,17.55002548,18.10465635,18.60172219\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,14.61428577,15.42724573,16.15438267,16.80735645,17.39550768,17.92652529,18.40688668\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], c1cnc(cn1)C1=NN=N[N]1, c1cnc(cn1)C1=N[N]N=N1, nodes [Co], topology \",,,15.06332407,15.80195967,16.45832988,17.04587965,17.57500512,18.05384495,18.48887072\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,17.05271384,17.65904713,18.14463637,18.53840507,18.86146286,19.12937999,19.35377754\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,16.58007791,17.23162836,17.75940548,18.19139768,18.54855386,18.84664782,19.09765584\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,4.67754713,5.070652831,5.50706157,5.976045699,6.46642404,6.968060639,7.472564152\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,4.676658324,5.069625111,5.505924434,5.974828092,6.465152402,6.966757887,7.471249373\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,4.705850357,5.083847701,5.50805935,5.967404267,6.450372687,6.946527052,7.447205513\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,4.669504968,5.065512584,5.504905103,5.976719275,6.469648227,6.973503204,7.479885191\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,4.704833889,5.082826809,5.507051442,5.966421033,6.449421675,6.94561283,7.446330522\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,4.66914369,5.065128878,5.504496379,5.97628636,6.469194081,6.973031919,7.479401279\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,9.642840117,10.12938619,10.63436726,11.1542131,11.68307589,12.21444641,12.74213047\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,9.643856299,10.1301321,10.63489174,11.15455756,11.68327495,12.21452872,12.74211954\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,9.65312694,10.12799846,10.6239466,11.13670414,11.66000107,12.18705387,12.71147099\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,9.654100101,10.13601938,10.6355313,11.14981046,11.67345923,12.20020684,12.7239557\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,9.654395708,10.12913757,10.62494832,11.137565,11.66072261,12.18764195,12.71193466\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,9.654059115,10.13589378,10.63533206,11.14954854,11.67314532,12.19985101,12.72356721\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.49747329,16.09400992,16.63128044,17.1206237,17.56951537,17.98307566,18.36500468\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,14.78482685,15.46826035,16.07998865,16.63298095,17.13630944,17.59652906,18.01857798\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.78306413,16.3408772,16.84255082,17.29961422,17.71962074,18.10764402,18.46723301\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.00664786,15.66795419,16.25742992,16.78897606,17.27225101,17.7141324,18.11969025\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.49629844,16.09305683,16.63046697,17.11989665,17.56884108,17.98243349,18.36438255\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,14.7848343,15.46818236,16.07983943,16.63277296,17.1360537,17.59623527,18.01825468\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.78450503,16.34200931,16.84344284,17.30031692,17.72017251,18.10807448,18.46756539\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.01250686,15.67321642,16.2621833,16.79329276,17.27619013,17.7177425,18.12301151\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.52157315,16.12182974,16.65732253,17.14146645,17.58330528,17.98906931,18.36319779\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,14.99239741,15.6493787,16.24075587,16.77806825,17.26917517,17.71967947,18.13380705\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,14.9875879,15.64515591,16.23705477,16.77482964,17.26634456,17.71720696,18.13164742\n\"linker [O-]C=O, nodes [Co], topology pcu,nbo\",,,15.52571606,16.12540687,16.66040952,17.14412841,17.5855989,17.99104416,18.36489724\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,21.52245909,21.77635033,21.97262211,22.12731829,22.25131093,22.35216311,22.43525952\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,21.62616002,21.86333485,22.04655473,22.19088459,22.30651811,22.4005383,22.47798341\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,21.59900142,21.84108014,22.02799627,22.17517789,22.29305591,22.38887328,22.4677791\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,21.53320215,21.78575315,21.980884,22.13461306,22.25778517,22.3579388,22.44043775\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,19.78631633,20.28659856,20.6832163,21.00223865,21.26223655,21.47665704,21.65539283\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,19.74115436,20.24688894,20.6481863,20.97120911,21.23462676,21.45197709,21.63323172\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,19.88803507,20.37096144,20.75422567,21.06278231,21.3144408,21.52211719,21.6953265\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,20.25064644,20.67593591,21.01406543,21.28666748,21.50925073,21.69310101,21.8465544\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.716008415,4.388084133,5.082430263,5.779776553,6.46558319,7.129743099,7.765886391\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.410396961,4.086186676,4.789083448,5.498193816,6.19764747,6.876335257,7.527175872\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.658263336,4.325664097,5.017492025,5.714068216,6.40042747,7.066083612,7.704356619\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.408414639,4.086196353,4.790955631,5.501738593,6.202642543,6.882547947,7.534378892\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.41127887,4.088620477,4.792948953,5.503329123,6.203869053,6.883453687,7.535007259\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.703478597,4.375339973,5.069953066,5.767880602,6.454454808,7.119475022,7.756505927\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.408585132,4.083974783,4.786405669,5.495052637,6.194086279,6.872418233,7.522974439\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,3.699794342,4.370006325,5.063166419,5.759907896,6.445570639,7.109931414,7.746520513\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,6.978148224,7.917466868,8.772563393,9.542994166,10.23268488,10.84781746,11.39548966\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,6.950257013,7.891721391,8.74880267,9.521074606,10.2124708,10.82917838,11.37830038\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,6.968306671,7.90646591,8.760984916,9.531252557,10.22106549,10.83650927,11.38461161\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,7.045802287,7.990595051,8.84867321,9.62010123,10.30930403,10.92289346,11.46831139\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.178852444,9.80183674,10.4418892,11.08911411,11.73395564,12.36813236,12.98502012\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.473956064,10.12317117,10.77649128,11.42788346,12.07062655,12.69847954,13.30627212\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.173062219,9.792392399,10.43073995,11.07767169,11.72317231,12.35859682,12.97705041\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.427738824,10.08159856,10.74006745,11.39676756,12.04471401,12.67748328,13.28979289\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.427444944,10.08067165,10.73868787,11.39506742,12.04279122,12.67541117,13.28762684\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.201041756,9.820953674,10.45947709,11.1062102,11.75120545,12.38589327,13.00344806\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.472945658,10.12296691,10.77680838,11.42852604,12.07146048,12.69941381,13.30724584\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,9.16128798,9.784236544,10.4244966,11.07212337,11.71750921,12.35232594,12.96991089\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.40503677,11.16023394,11.90946851,12.64348003,13.35413208,14.03515116,14.68224495\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.681705,11.45000639,12.20637395,12.94304528,13.65294782,14.33060538,14.97235043\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.50990881,11.2505021,11.98837259,12.71347749,13.41706937,14.09240715,14.73484747\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.69979379,11.46427621,12.21750211,12.95164312,13.65953898,14.33562299,14.97614421\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.69375033,11.45943708,12.21367043,12.9486438,13.65722142,14.33386029,14.97483088\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.49998942,11.24187217,11.98084447,12.70689775,13.41130881,14.08735526,14.73040901\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.65577342,11.42900286,12.18925661,12.92902923,13.64142791,14.32110734,14.96449825\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,10.49607301,11.2407058,11.98100064,12.70738818,13.41149692,14.08686863,14.72906317\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,11.08304676,11.75716705,12.42954473,13.0922823,13.7381605,14.36131292,14.9574242\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,11.0534282,11.73016772,12.40488633,13.06972713,13.71749872,14.34235665,14.94000447\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,11.12283499,11.79656633,12.46921365,13.13245866,13.77882116,14.4022917,14.99849116\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,11.12229961,11.7971362,12.47054841,13.13431444,13.78102215,14.4047108,15.00103648\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,17.59695223,18.4506883,19.15592453,19.74247371,20.23383999,20.64845289,21.00076948\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,17.18584989,18.09098085,18.8396642,19.46296524,19.98551228,20.42669157,20.80175371\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,18.28593872,19.05428318,19.68690277,20.21177253,20.65066047,21.02047387,21.3343831\n\"linker [N]1C=NN=C1, nodes [OH], [Zn], topology pcu\",,,18.26600975,19.04338611,19.68198346,20.21082201,20.65233636,21.02386828,21.33887638\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,19.38887641,19.94699669,20.39515911,20.75951262,21.05913394,21.30812083,21.51702642\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,19.39275713,19.95043856,20.39821473,20.76223234,21.06156301,21.31029863,21.51898671\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,19.39253968,19.95022221,20.39800665,20.76203588,21.06137944,21.31012806,21.51882868\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,19.38897985,19.94709709,20.39525411,20.75960129,21.05921611,21.30819669,21.51709637\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.332616707,3.988480611,4.667613241,5.352706016,6.030138997,6.690046545,7.32590054\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.330917057,3.986616157,4.665637422,5.350665555,6.028072238,6.687983539,7.323863964\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.330726801,3.986405654,4.665418513,5.350447223,6.027860847,6.687783299,7.323677416\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.332902719,3.988773756,4.667903765,5.352986623,6.030404746,6.690294454,7.326129125\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.340348971,4.001932608,4.686436865,5.376272576,6.057683065,6.720769862,7.359039078\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.337898553,3.999340485,4.683776058,5.373601907,6.055046774,6.718199308,7.356555144\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.337551465,3.998932292,4.683318487,5.373106957,6.05452571,6.717662108,7.356010279\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.340798323,4.002395955,4.686903135,5.376732772,6.058130429,6.721199672,7.359448296\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.758536627,7.603820442,8.388373749,9.109464323,9.767529135,10.36510797,10.90600115\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.75924945,7.605266131,8.390397693,9.111920425,9.770290017,10.36806832,10.90907715\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.752420448,7.598308584,8.383437887,9.105055124,9.763590359,10.36158391,10.90284017\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.765515716,7.610913136,8.395463473,9.116458702,9.774358468,10.3717226,10.91236816\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.487877393,4.161871263,4.855927666,5.552456248,6.237904522,6.902687113,7.540662946\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.487776553,4.161753427,4.855794954,5.552311344,6.237750272,6.902526251,7.540497941\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.4974774,4.176028994,4.874395997,5.574739031,6.263378103,6.930692543,7.570566661\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,3.497402279,4.175953047,4.874322433,5.574669845,6.263314382,6.930634744,7.570514824\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.484096909,7.277150425,8.063786948,8.83835229,9.596304843,10.3337875,11.04752999\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.713245891,8.499296319,9.270828415,10.02557676,10.76061117,11.47281157,12.15928951\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.315795844,10.09443998,10.85065249,11.58045717,12.28043222,12.94805455,13.58175762\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.481387489,7.274598561,8.061417845,8.836173456,9.59431263,10.33197186,11.04587767\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.712750429,8.49886728,9.27044638,10.02522708,10.76028331,11.4724983,12.15898612\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.316653534,10.09536416,10.85162957,11.58147499,12.28147946,12.94912075,13.58283332\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.482281407,7.275305823,8.061962635,8.836582841,9.594612713,10.33218584,11.04602515\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.712566008,8.498662668,9.270229545,10.02500441,10.76005978,11.4722777,12.15877116\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.316792213,10.09531881,10.85141959,11.5811227,12.28100785,12.94855192,13.58218752\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.482730536,7.276002278,8.062833751,8.837567401,9.595661928,10.33326248,11.04710187\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.713403548,8.499457048,9.270983374,10.0257205,10.76074066,11.47292551,12.15938772\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.316590285,10.09532533,10.85162117,11.58149699,12.28152884,12.9491933,13.58292462\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.519478647,7.314599471,8.103981977,8.881685095,9.642872464,10.38344242,11.09995027\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.727965676,8.517311111,9.292423719,10.05073807,10.78909888,11.50424049,12.19319745\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.327308056,10.10490172,10.86006965,11.58885689,12.28786973,12.95460729,13.58751603\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.517835941,7.312890102,8.102239014,8.879931029,9.64112309,10.38170926,11.09824201\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.727784366,8.517035482,9.292043208,10.05025094,10.78851006,11.50355935,12.19243593\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.328094001,10.10571198,10.86089337,11.589685,12.28869457,12.95542255,13.58831663\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.518048186,7.31310142,8.102458608,8.880164965,9.64137443,10.38197866,11.09852842\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.727723943,8.51703526,9.292105276,10.05037417,10.78869084,11.50379237,12.19271487\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.327653208,10.10516852,10.86025697,11.58896926,12.28791461,12.95459337,13.58745214\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,6.518968584,7.314076916,8.103437087,8.881111541,9.642267664,10.38280696,11.09928705\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.727887152,8.517152316,9.292186631,10.05042701,10.7887202,11.50380195,12.19270761\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.328078803,10.10569997,10.86089464,11.58970347,12.28873066,12.95547482,13.58838284\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.34733401,10.12697037,10.88462824,11.61574373,12.31663771,12.98471318,13.61842219\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.453881346,8.279699837,9.08685149,9.872423286,10.63361682,11.3677751,12.07257386\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.347210655,10.12685519,10.88452032,11.61564247,12.31654267,12.98462398,13.61833849\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.453842309,8.279642278,9.086779864,9.872340841,10.6335261,11.36767817,12.07247248\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.346031465,10.12913836,10.89022073,11.62454309,12.32831858,12.99889465,13.63470666\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.446501158,8.274411322,9.08300379,9.869457614,10.63109758,11.36538789,12.07010828\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,9.346188812,10.12928125,10.8903533,11.62466814,12.32843796,12.99900953,13.63481775\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,7.446552848,8.27445887,9.083044073,9.869488885,10.63111911,11.36539967,12.07011079\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.52690897,15.33081171,16.0498777,16.69563864,17.27769407,17.80402547,18.28129976\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.41401996,15.21095892,15.92827305,16.57547969,17.16088623,17.6916505,18.17391633\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.5263303,15.33021195,16.04919576,16.69485273,17.27680407,17.80304236,18.28023939\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.41577152,15.21246521,15.92957417,16.57660759,17.16186723,17.69250666,18.17466628\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.52529709,15.32946323,16.04874013,16.69467184,17.27686678,17.80331301,18.28068243\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.41254773,15.20953305,15.92692306,16.57422031,17.15972281,17.69058261,18.17294013\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.52779264,15.33145873,16.05025718,16.6957546,17.27756879,17.80368944,18.2807858\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.41480959,15.21175693,15.92905945,16.57624186,17.16161692,17.69234615,18.17457575\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.61314489,15.41375307,16.13103257,16.77589668,17.35749835,17.88351338,18.3604137\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.56884843,15.35343393,16.05815678,16.69313202,17.26701581,17.78714579,18.25973513\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.61011234,15.41103652,16.12857473,16.77365377,17.35543684,17.88160741,18.3586431\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.56869034,15.35266607,16.0570103,16.69175576,17.26550678,17.78556798,18.25813115\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.60977658,15.4107015,16.12826321,16.77337872,17.35520432,17.88141887,18.35849708\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.56946048,15.35362339,16.05806559,16.69285414,17.26661433,17.7866637,18.25920211\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.61386072,15.41443371,16.13165396,16.77644605,17.35797099,17.88391001,18.36073841\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,14.56630456,15.35096797,16.05580374,16.69090618,17.26492009,17.78517714,18.25788757\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,16.8392615,17.75727772,18.52382283,19.16754472,19.71150625,20.17410232,20.56997564\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,16.84275495,17.76072827,18.52713676,19.17067884,19.71444459,20.17684357,20.57252625\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,16.83918293,17.75713284,18.52364128,19.16734611,19.71130298,20.17390195,20.56978256\n\"linker [O-]C(=O)c1cc(cc(c1)C(=O)[O-])c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [Ga], [OH], topology \",,,16.847008,17.76456218,18.53059355,19.17379893,19.7172657,20.17939999,20.57484863\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.78691066,18.50383168,19.1259049,19.66662636,20.13763787,20.548949,20.90912783\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.32390681,17.14325363,17.86456672,18.49959668,19.05897193,19.55223284,19.98786118\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,18.07636289,18.81227799,19.44527222,19.98974059,20.45877448,20.86386135,21.21485617\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.66538442,18.3916259,19.02279728,19.57213741,20.05114894,20.46978624,20.83661593\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.28782614,17.10456977,17.82407122,18.45812899,19.01727503,19.51090417,19.94735036\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,18.17741555,18.90764207,19.53439011,20.07251075,20.53537152,20.93461403,21.28016858\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.30761091,17.10523003,17.81223845,18.43843455,18.99287898,19.48393047,19.91920922\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.36613606,17.17170524,17.88174472,18.50784802,19.06032547,19.54836419,19.98011534\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,19.37046198,19.95036189,20.44877125,20.8777655,21.24787111,21.56812213,21.84618208\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.3727175,17.16035699,17.86043503,18.48159884,19.03219642,19.52015515,19.952837\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.38885002,17.19323944,17.90164042,18.52597493,19.07672241,19.56314983,19.99343962\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,19.53471938,20.09644512,20.57874192,20.99367837,21.35159737,21.66129825,21.93021232\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,20.87007074,21.41170623,21.83977212,22.18315765,22.46235318,22.69213585,22.88333719\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,21.06285678,21.57598314,21.98109014,22.30581198,22.56968538,22.78676674,22.96734144\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,21.0494826,21.56441806,21.97102606,22.29699077,22.5618974,22.77984352,22.96114761\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,21.03182685,21.54935689,21.95808069,22.28578249,22.55212539,22.77126747,22.95357443\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,21.48425551,21.93829593,22.29512173,22.58010174,22.81099646,23.00048583,23.15779023\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,21.5757866,22.01410517,22.3588865,22.63444578,22.85783855,23.0412603,23.19359017\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,21.2887303,21.77186718,22.15205769,22.4559994,22.70244521,22.90481755,23.07289597\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,21.40809756,21.87213846,22.23735927,22.52937264,22.76617464,22.96064902,23.12218452\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.3545521,3.987428801,4.646849358,5.315765064,5.980449278,6.630728767,7.259676398\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.022393504,3.629758011,4.270987706,4.928433219,5.58751586,6.237123233,6.869407469\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.434268545,4.068273697,4.728310222,5.397370327,6.061742068,6.711271549,7.339065409\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.52858221,4.162694902,4.820258278,5.484992275,6.143869127,6.787287555,7.408758736\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.308206471,3.93522645,4.589955691,5.255192572,5.917107437,6.565430369,7.193130661\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.435768795,4.059410521,4.70810599,5.365923703,6.019890471,6.660283206,7.280400439\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.341924776,3.973133032,4.631540582,5.300004457,5.964677316,6.615267739,7.24474671\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,2.98992257,3.591523626,4.22803007,4.881870269,5.538416345,6.18643771,6.817940287\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.436836092,4.070280038,4.729745267,5.398249105,6.062101216,6.711162792,7.338548779\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.521538508,4.154781687,4.81162227,5.475784977,6.134236727,6.777363138,7.398657552\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.300218319,3.926496244,4.580603354,5.245349876,5.906909434,6.555008077,7.182605762\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.436910372,4.06053495,4.708817787,5.365965423,6.019109872,6.658596968,7.277763492\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.414570577,4.045839135,4.701679327,5.365723953,6.024849314,6.669348686,7.292621686\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.093540561,3.697701455,4.336005728,4.990739988,5.64726694,6.294429691,6.924351586\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.448005055,4.076562456,4.731481328,5.395924551,6.056272437,6.702399864,7.32739709\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.35919114,3.978905001,4.625413982,5.28237219,5.936535166,6.577997955,7.199929465\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.196844364,3.790393669,4.416993543,5.059702842,5.704490126,6.340607022,6.960409644\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.50125376,4.134168541,4.792183693,5.458532328,6.119731913,6.765813633,7.390018835\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.414039252,4.046296954,4.703430292,5.368893456,6.029430493,6.675249126,7.299701916\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.084144689,3.68975922,4.329353978,4.985195497,5.642646808,6.290562286,6.921081431\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.455300901,4.084206206,4.739382996,5.403984229,6.064393789,6.710497546,7.335399905\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.349777353,3.96717257,4.61150842,5.266562926,5.919146022,6.559356941,7.180337538\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.121063568,3.706561266,4.327436964,4.96664508,5.609889439,6.246102714,6.867327861\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,3.502423942,4.135482318,4.793550583,5.459885905,6.121026131,6.767018769,7.391117583\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.587271189,10.31761254,11.03039332,11.72254394,12.3909653,13.03297252,13.64651802\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.669482761,10.38370659,11.08457852,11.76865008,12.43200474,13.07109645,13.68314238\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.376488837,10.11597569,10.84359359,11.55350284,12.24063977,12.90103468,13.53187277\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.984377293,8.703392928,9.422063055,10.13692089,10.8430834,11.53533683,12.20885903\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.161932217,7.952206373,8.730427724,9.492062462,10.23369728,10.95251477,11.6461416\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.571356793,10.29880192,11.01203162,11.70668494,12.37873282,13.02485012,13.64256888\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.680413106,10.38562469,11.08102455,11.76212866,12.42424121,13.06324268,13.67593542\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.30311178,10.04939898,10.78415067,11.5012447,12.19535609,12.862318,13.49918971\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.910349691,8.636118292,9.361051201,10.08166961,10.79310094,11.49015092,12.16802154\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.121686293,7.908499324,8.685110217,9.4467661,10.18973379,10.91085257,11.60743059\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.584744575,10.31284359,11.02378216,11.7144559,12.38172643,13.02286709,13.63578873\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.664048116,10.37532128,11.07403394,11.7566143,12.41901918,13.05758469,13.66942568\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.386301801,10.12420959,10.85047485,11.55922576,12.24537196,12.90492075,13.53503721\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.986133307,8.704854717,9.423334084,10.13808196,10.84419314,11.53643462,12.20996887\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.143751642,7.935038402,8.714492139,9.477495157,10.22055665,10.94079676,11.63579654\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.576202552,10.30296292,11.01578696,11.71021859,12.38216136,13.0282428,13.64596241\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.686318017,10.39143356,11.08686039,11.76805851,12.43028948,13.06940445,13.68218774\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.281677388,10.03028863,10.76712526,11.48607331,12.18182085,12.85021759,13.48834106\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.91517016,8.63971285,9.363770861,10.08376435,10.79474957,11.49148161,12.1691261\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.126641526,7.912501143,8.688576419,9.450055218,10.19312239,10.91453305,11.61152058\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.587651415,10.32065016,11.03786942,11.7351643,12.40875486,13.05555692,13.67331543\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.72439832,10.42350902,11.11474061,11.79304302,12.45326595,13.09095169,13.70266642\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.429328722,10.16268599,10.88587013,11.59268824,12.27772264,12.9366976,13.56655663\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.952879309,8.672357663,9.392952369,10.11068776,10.82026775,11.51616184,12.1933194\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.138129381,7.928577744,8.70783563,9.471190722,10.21501875,10.93630245,11.6325015\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.681863024,10.40597078,11.11529667,11.80555376,12.47284516,13.11399029,13.7266553\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.80023319,10.48052063,11.15740188,11.82475847,12.47661969,13.10790223,13.71469783\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.378314994,10.11413391,10.8405977,11.55106063,12.23981262,12.90239718,13.53565296\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.942373347,8.668572438,9.396013871,10.12029133,10.83582731,11.53693565,12.21850598\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.101716363,7.896997166,8.681132103,9.449377238,10.19799111,10.92383037,11.62425404\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.614280178,10.34385004,11.05769451,11.75179612,12.42245358,13.06662212,13.68205766\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.708718039,10.4102498,11.10333817,11.78306957,12.44440171,13.08295997,13.69537299\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.441779634,10.17356462,10.89524453,11.60063744,12.28434301,12.94210036,13.57086187\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.937332814,8.657251337,9.378384341,10.09670237,10.80687982,11.50336978,12.18111233\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.136503781,7.926287141,8.705118585,9.468182505,10.21180148,10.93293184,11.62902004\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.679143055,10.40184796,11.10951059,11.7980622,12.46374907,13.10347295,13.7149378\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.794460313,10.47146479,11.14520088,11.80976882,12.45929428,13.08871324,13.6940931\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.380344655,10.11699155,10.84375965,11.55419641,12.24272799,12.90499071,13.53788397\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.936781582,8.66446412,9.39307811,10.11827949,10.83454106,11.53621715,12.21822972\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,7.100436196,7.899141043,8.685996198,9.456441392,10.20684613,10.93413803,11.63572586\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.982128352,10.85084678,11.67761898,12.46227775,13.20463253,13.90471727,14.56293307\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.27069943,11.11458759,11.91771635,12.68033,13.40249598,14.08434375,14.72624276\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.06768674,10.94034944,11.77005285,12.55669706,13.30017041,14.00059743,14.65847761\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.33836136,11.18520821,11.99114236,12.75612843,13.48008531,14.16308916,14.80551996\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,9.965420726,10.83292869,11.65897474,12.44328002,13.18556681,13.88580004,14.54432577\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.35129682,11.19165587,11.99134083,12.75058362,13.46945186,14.14808303,14.78685807\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.17552258,11.03962484,11.86140556,12.64078249,13.37762686,14.07202773,14.72444039\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.33211462,11.1788063,11.98473952,12.74984868,13.47401841,14.15729387,14.80003004\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.13386902,11.00244453,11.82825512,12.6112196,13.35124011,14.04844484,14.70332875\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.42136607,11.27723074,12.08917617,12.85765098,13.58307525,14.26598221,14.90714215\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.08970253,10.95256316,11.7751628,12.55675514,13.29671384,13.99476298,14.65109614\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.483787,11.32288692,12.12171396,12.88004638,13.59769817,14.27469073,14.91137858\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.138612,11.00658218,11.83195981,12.61459099,13.35433861,14.05130963,14.70598732\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.38578817,11.24306562,12.05653414,12.82657746,13.55357184,14.23802122,14.8806766\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.07192562,10.93362596,11.75496904,12.53535925,13.27427422,13.97149621,14.62724057\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,10.45492853,11.29663729,12.09761366,12.8577442,13.57693143,14.25526358,14.89314306\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.50084631,16.23768911,16.89352026,17.4812626,18.01095535,18.49049094,18.92617687\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.56655996,16.28554878,16.92906954,17.5079045,18.03084967,18.50507641,18.93646862\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.47279294,16.21730597,16.87856109,17.47005001,18.00226859,18.4834618,18.92020129\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.1695985,15.95132878,16.64785453,17.27154057,17.83246088,18.33884016,18.79744503\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.9356575,17.65126318,18.29023153,18.86228848,19.37481626,19.83405838,20.24560166\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.76620259,16.78360304,17.66448697,18.42624988,19.08538889,19.6567764,20.15341591\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.33795398,17.28559676,18.10622815,18.81636109,19.43137833,19.96504077,20.4293446\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.92342629,17.75954098,18.49118419,19.13068919,19.68967632,20.17877665,20.6074837\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.63308855,17.4035395,18.08839668,18.69810773,19.24120735,19.72514306,20.15659696\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.00686924,17.70282139,18.32771022,18.88954466,19.39457194,19.84826427,20.25567303\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.56106614,18.31913313,18.98422297,19.5670807,20.07778694,20.52560764,20.91887552\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.32783082,16.08665931,16.76084533,17.36403313,17.90681841,18.39752626,18.84280385\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.61789427,16.33310416,16.97302609,17.54851161,18.06837781,18.53979281,18.96862579\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.4702938,16.21634049,16.87868531,17.47097044,18.00378202,18.48542112,18.92249595\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.20199751,15.9830786,16.67884702,17.30171854,17.86178868,18.3672917,18.82500008\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.02742804,17.73351455,18.36464186,18.9300521,19.43682431,19.89100722,20.29805736\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.71671008,16.73775405,17.62242197,18.38784108,19.05038401,19.62487661,20.12431659\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.39185928,17.33108127,18.14481805,18.84932504,19.45974449,19.98963289,20.45082031\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.00155605,17.83344058,18.56025827,19.19480623,19.74896434,20.2334991,20.65796588\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.42978743,17.21875974,17.91909364,18.54219118,19.09714289,19.59172561,20.0328255\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.96370885,17.66443095,18.29323384,18.85836436,19.36622137,19.82237717,20.23195217\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.4535648,18.16634953,18.80180915,19.36692439,19.86859955,20.31359222,20.70833213\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.37715754,16.12894798,16.8005153,17.40367691,17.9478396,18.44056173,18.88800879\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.80320735,16.50522147,17.12944071,17.68855776,18.19245442,18.64888209,19.0639953\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.07068538,15.85287066,16.55134628,17.17828174,17.74343883,18.25471065,18.71856751\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.5304796,16.28351661,16.94814038,17.53961787,18.06967623,18.54741413,18.97999065\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.72869272,17.48257801,18.15307966,18.75074396,19.28391677,19.75975575,20.18464076\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.62958877,17.38182324,18.05201248,18.65065683,19.18588351,19.66458506,20.09289132\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.90195328,16.84392213,17.67171727,18.39682671,19.03120992,19.58636788,20.07284468\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.55379168,17.39527104,18.135835,18.78738662,19.36067439,19.86544581,20.31045776\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.68386595,17.401302,18.04542908,18.62493807,19.14644433,19.61559967,20.03753715\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.37020126,17.12686604,17.80334084,18.40980868,18.95402498,19.44250319,19.88102957\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.28211003,17.2429743,18.0758794,18.79638748,19.41973713,19.95988111,20.42911441\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.5498995,16.27821449,16.92960105,17.51542819,18.044712,18.52466962,18.96116845\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.90648764,16.59233567,17.20408417,17.75346983,18.24967525,18.69993899,19.11003876\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,14.76942755,15.59143352,16.32252114,16.97647427,17.56424899,18.09463344,18.57477792\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.48208735,16.24451783,16.91651946,17.51387632,18.04867452,18.53026794,18.96600201\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.61551872,17.3878531,18.07394144,18.68456853,19.22843087,19.7130512,20.1451448\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.67529902,17.41423357,18.0736621,18.66379976,19.19242103,19.66606983,20.09056441\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,15.89997374,16.88825028,17.74949687,18.49751435,19.14664185,19.7104497,20.2011447\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,17.05051555,17.8547723,18.56159615,19.18207069,19.72659223,20.20474604,20.62518735\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.72294726,17.43358804,18.07211046,18.64705033,19.16484984,19.63100057,20.0504985\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.45261242,17.20829289,17.88337341,18.48793873,19.02978799,19.51553738,19.95108875\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.25082464,17.2234312,18.06488345,18.79153221,19.41924303,19.96244624,20.43379197\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.79891803,17.67540418,18.44148348,19.10866816,19.68906681,20.19426255,20.63476822\n\"linker [O-]C(=O)c1cnccn1, nodes [Ni], [O], [V], [V][V], topology \",,,16.35160003,17.23387977,18.01213824,18.69591344,19.29560439,19.82146453,20.28304262\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,20.09142352,20.39694945,20.63800422,20.83125508,20.98839393,21.11778906,21.2255428\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,20.02626633,20.33883731,20.58608263,20.78473194,20.94656751,21.08005092,21.19137062\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,2.787438395,3.411032073,4.074032526,4.756219287,5.441401896,6.117619467,6.77669372\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.531006074,4.175535596,4.839069086,5.506294254,6.165159441,6.806903365,7.425702555\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.385263414,4.072779646,4.781498705,5.492288711,6.190956548,6.867797119,7.516812063\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.861336579,4.52675823,5.203408585,5.87694472,6.536430821,7.174179458,7.785313537\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.239756005,3.912541116,4.608128799,5.308203948,5.998872,6.670381297,7.316487963\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.350826117,3.986706049,4.645525499,5.3113658,5.971548296,6.616739956,7.240629543\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.471615404,4.160767489,4.867471398,5.573833114,6.266555677,6.936518134,7.578068463\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.084915886,3.689831848,4.32574333,4.976237178,5.627768246,6.27002809,6.895760111\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,4.06589541,4.724402666,5.38834193,6.046440646,6.689289387,7.309671308,7.902506756\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.457405079,4.102765381,4.767787348,5.436938795,6.098075584,6.742416756,7.364153068\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.78018337,4.436920514,5.102434912,5.764809163,6.414335876,7.043773701,7.648239834\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.673608714,4.337265779,5.014469147,5.6903884,6.353732679,6.996555499,7.613787059\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,2.930542948,3.573924818,4.233156819,4.893967167,5.545907343,6.181670998,6.796463848\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.308114421,3.935609614,4.587449745,5.247853761,5.904126316,6.546838678,7.169548496\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.081901474,3.734907786,4.398985054,5.06089057,5.711098738,6.343045585,6.952499882\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,3.176856028,3.783423648,4.418564203,5.066508721,5.714290171,6.352070747,6.972951864\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.193957394,9.909665802,10.62111282,11.32093682,12.00234556,12.6598374,13.28940716\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.502147413,10.27545183,11.01882162,11.73002249,12.40769456,13.05112421,13.66012832\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.143106218,9.844566098,10.54235627,11.22982088,11.90060111,12.54936783,13.17208947\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.550022446,10.32258461,11.0645836,11.77367649,12.44859337,13.08879289,13.69427601\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.035086306,9.765927388,10.48548819,11.1889752,11.87161506,12.52929675,13.15886877\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.584383019,10.34668992,11.07680802,11.77410661,12.43826499,13.06918659,13.6670079\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.057372117,9.777009099,10.48508686,11.1774179,11.84967444,12.49802494,13.11945446\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.641347522,10.39149712,11.10929978,11.79467925,12.44769911,13.06850948,13.65738295\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.628286365,10.40844445,11.15675701,11.87124038,12.55075401,13.19478878,13.80335555\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.671670497,10.44401097,11.1826936,11.88660778,12.55534619,13.18895133,13.78780632\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.505846285,10.27704058,11.01695402,11.72428704,12.39821966,13.03831931,13.64452389\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.609954966,10.36381663,11.08626707,11.77667064,12.43470087,13.06025579,13.65346064\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,7.856110769,8.62262802,9.384502662,10.1361529,10.87186705,11.58641948,12.2754616\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,7.475914992,8.230586641,8.978602915,9.716087836,10.43877623,11.14246224,11.82338603\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,7.817380594,8.576577059,9.332273133,10.07872423,10.81013744,11.52123379,12.20761289\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,7.519793865,8.244594384,8.964553231,9.676452921,10.37646342,11.06058416,11.72506478\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,7.694937457,8.462836233,9.222845578,9.970547774,10.7013121,11.41077502,12.09519829\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,8.025301617,8.773081152,9.511522872,10.23760253,10.94748901,11.63725227,12.3033624\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,7.710593956,8.480629806,9.245141234,9.998696195,10.73586574,11.45170595,12.14208991\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,7.931925568,8.687566812,9.433584176,10.16693901,10.88377746,11.5801326,12.25243375\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.607659364,10.38357217,11.15185638,11.90433813,12.63349727,13.33330204,13.99945896\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.42202255,11.1438287,11.85060882,12.53679003,13.19716868,13.82765347,14.42549405\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,9.588931339,10.33985836,11.08661707,11.82123997,12.53613519,13.2250052,13.88318057\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.44055013,11.13424079,11.81504431,12.47827659,13.11915375,13.73364141,14.31880397\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.35287342,11.19086466,11.996872,12.76713445,13.49842575,14.18854531,14.83642864\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,11.35303458,12.30856526,13.19828155,14.02043064,14.77560773,15.46620091,16.09578884\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.42553205,11.24844043,12.04078239,12.79891788,13.51965958,14.20076631,14.84107387\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,11.27683043,12.22737806,13.1135741,13.9334973,14.6876004,15.37813968,16.00857398\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.83580531,11.70629993,12.54476178,13.34431825,14.09967432,14.80761913,15.46690223\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.80199864,11.6774892,12.52014072,13.32306742,14.08108463,14.79112223,15.45206102\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.52775117,11.2947991,12.0473188,12.77851052,13.4821022,14.15320418,14.78853988\n\"linker N1=C[C](N[N]1)c1ccc(cc1)c1[nH]nnc1, nodes [Cu], topology pts,\",,,10.48482751,11.22227657,11.95090847,12.66364991,13.35367081,14.01538894,14.64481027\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,18.77337213,19.46045982,20.02488843,20.49264453,20.88359539,21.2130074,21.49269277\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,18.88215116,19.55700262,20.11094306,20.56966633,20.9528015,21.27542051,21.54917609\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,20.46808318,20.9259335,21.29295253,21.59106344,21.83610237,22.03969647,22.2105132\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,20.729014,21.15994875,21.50360332,21.78151582,22.00910383,22.19759969,22.3553203\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,20.4990376,20.95671398,21.32341754,21.62114307,21.86577029,22.06895209,22.23937053\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,20.49788224,20.96393355,21.33573711,21.6364726,21.88276972,22.08676167,22.25744105\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,12.29655936,13.22933809,14.09653758,14.89800809,15.63484776,16.30938396,16.9249056\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,11.38652422,12.32759077,13.215059,14.04478457,14.81490868,15.52559119,16.17855156\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,11.51272728,12.54441601,13.49993812,14.37810361,15.18054887,15.91080424,16.57354186\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,12.35379777,13.28226902,14.14528046,14.94276902,15.67586848,16.34691644,16.95919942\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,11.38366749,12.32861438,13.21875358,14.05027596,14.82156714,15.53296433,16.18631547\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,11.49564688,12.52908801,13.48620816,14.36577424,15.16942309,15.90070419,16.56431463\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,4.214784919,5.022058111,5.813423502,6.575515119,7.299981747,7.982405895,8.621314948\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,3.937928789,4.724737382,5.502884791,6.257786565,6.97990026,7.663708224,8.30676459\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,4.216367187,5.024339433,5.816231937,6.578708401,7.303443102,7.986040803,8.625048135\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,3.948671776,4.736065052,5.51426494,6.268833521,6.99034138,7.673350185,8.315466117\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,10.17586484,10.98619922,11.72839649,12.41129522,13.04324275,13.63138164,14.18148166\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,10.30692428,11.09028227,11.79605901,12.4356063,13.01959295,13.55717652,14.05578703\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,7.394588651,8.139707545,8.870962823,9.586888602,10.28569985,10.96537036,11.62383403\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,7.463774517,8.216889785,8.95643341,9.680628881,10.3873707,11.07435424,11.73930485\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,10.18495287,10.99703663,11.74081922,12.42520155,13.05856169,13.64805378,14.19944872\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,11.18376561,11.96808442,12.67537242,13.31674971,13.90274437,14.44241737,14.9431269\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,7.382546355,8.127158245,8.85821893,9.574175778,10.27318199,10.95316648,11.61202968\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,7.462581284,8.212057304,8.948545457,9.670199298,10.37486057,11.0601764,11.72382469\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.49131474,15.39657427,16.20731938,16.93442666,17.58691286,18.17262955,18.69860948\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.49631349,15.37818641,16.17312657,16.88983241,17.535765,18.11766397,18.64176442\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.61753865,15.49923614,16.2891101,16.99827699,17.63567572,18.20890734,18.72468025\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.61932714,16.42860254,17.14771768,17.78700006,18.35548239,18.86128083,19.31173128\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.18177507,15.09034177,15.90439668,16.63552866,17.29315115,17.88522421,18.41869315\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.2811154,15.19542326,16.01470429,16.74992528,17.41024086,18.00359887,18.53707413\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,13.80584984,14.88738792,15.84847623,16.69927815,17.45093015,18.11458494,18.7008169\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.60463199,16.36113407,17.04084999,17.65185498,18.20098648,18.69440285,19.13779152\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.59292518,15.4377208,16.19939996,16.88775913,17.51045297,18.07390382,18.58378623\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.28577253,15.19291349,16.00546306,16.73497824,17.39077679,17.98075769,18.51185521\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.64879682,16.53945599,17.32571489,18.01995363,18.63324686,19.17552456,19.65564598\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.28133008,15.29793704,16.20413581,17.00870623,17.72146665,18.35237739,18.91097492\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.04190702,15.79611886,16.46471784,17.06085997,17.59547811,18.0775244,18.51427961\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.99756699,15.77871386,16.46744331,17.07882272,17.62508471,18.11607232,18.55968793\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.8782227,15.62358517,16.29178338,16.89504211,17.44245289,17.94097528,18.39613208\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.17247136,15.89742435,16.54880202,17.1380684,17.67362114,18.16186109,18.60788876\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.35734938,15.18743717,15.93981657,16.62149396,17.23910613,17.79883571,18.30637469\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.07451097,14.93270799,15.70889823,16.41108837,17.04659077,17.6220666,18.14356255\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,16.55392261,17.09124569,17.56686588,17.99361251,18.38076472,18.73506233,19.06144857\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,10.79337505,11.22223427,11.60939865,11.96386087,12.29172736,12.59716353,12.88305467\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.78036336,15.66140046,16.45060794,17.1584482,17.79360631,18.36367496,18.87548238\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.5059037,15.3828138,16.17373946,16.88713673,17.53029904,18.10984753,18.63193152\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.6527643,15.5309072,16.31788922,17.02460783,17.65986823,18.23119035,18.74523298\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.77288664,16.55016744,17.2436582,17.86221368,18.41376725,18.90560852,19.34444724\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.19496088,15.10050453,15.91214506,16.6413694,17.29749439,17.88839623,18.42095087\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.23039333,15.15314115,15.97964067,16.72093955,17.3863183,17.98386547,18.52079306\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,13.56727247,14.6649066,15.64234826,16.50903698,17.27570232,17.95329817,18.55233059\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.44023135,16.21770215,16.91450344,17.53965536,18.1006615,18.60416018,19.05619264\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.63228579,15.47123391,16.22813967,16.91257723,17.532031,18.092791,18.6004276\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.42116669,15.30932615,16.10613105,16.82254843,17.46740657,18.04820505,18.5715552\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.72626068,16.61677713,17.40230294,18.09511858,18.70637681,19.24615016,19.72344753\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.17224306,15.19401913,16.10535321,16.91509181,17.63301917,18.26902793,18.83258666\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.02364849,15.77871419,16.44879251,17.04669068,17.58313411,18.06695669,18.50537635\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.29249397,16.03606342,16.6940122,17.27985552,17.80467981,18.27747419,18.70549791\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.42670924,16.10068651,16.7107544,17.26608058,17.77352195,18.23837723,18.66491598\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,15.1765286,15.90562502,16.55930392,17.1496289,17.68541832,18.1733648,18.61876902\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.26032499,15.09439103,15.85092735,16.53689933,17.15885431,17.72288451,18.23460856\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,14.03942351,14.89889232,15.67657764,16.38046208,17.0177966,17.59517603,18.11858968\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,16.50163412,17.06524318,17.56229446,18.00671391,18.40859102,18.77527253,19.11216205\n\"linker [O-]C(=O)C(=O)[O-], [O]P(=O)(O)[O], [O]P(=O)([O])O, [O]P(=O)([O])[O], nodes [Ga], [Mn], topology \",,,17.23451275,17.66665,18.05631239,18.41275233,18.74223159,19.04901166,19.33603906\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,21.40838555,21.76332275,22.03914464,22.25754363,22.43332358,22.5768401,22.69550048\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,20.93934831,21.36546772,21.69799894,21.96214813,22.17528224,22.34964013,22.4940276\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.656554904,4.337002691,5.038393534,5.741458477,6.431862518,7.09975225,7.738989281\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.52522435,4.19471846,4.888735092,5.587582413,6.276419185,6.94488906,7.586397899\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.656812193,4.337499942,5.03905123,5.742218198,6.43268066,7.100596085,7.739834303\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.532366282,4.202579522,4.897256884,5.596656446,6.285914656,6.954672328,7.596344408\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.145437737,3.621788077,4.131481838,4.666168689,5.216753653,5.77466006,6.332543565\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,2.956703094,3.403292685,3.886374691,4.39881192,4.931996247,5.477323537,6.027102299\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.370823817,3.84015294,4.344773177,4.875183317,5.421578251,5.974989555,6.527898324\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.432460922,3.930304657,4.46313994,5.019263675,5.587714008,6.159113067,6.726010972\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.100011748,3.542071686,4.02172518,4.530923886,5.060633727,5.602103771,6.147641814\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.260262343,3.724542274,4.225552379,4.753825982,5.299477152,5.853386512,6.407848533\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,2.949049155,3.395137809,3.877990117,4.390404995,4.923716254,5.469271756,6.019342647\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.143357567,3.619256044,4.128831181,4.663640263,5.214506274,5.77278813,6.33109513\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.372867317,3.842085476,4.346598982,4.876902408,5.423189574,5.976491239,6.52928733\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.439858131,3.937375608,4.469756814,5.025358003,5.593260416,6.164113669,6.730483303\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.249498813,3.715143827,4.21735612,4.746672318,5.29321595,5.847880084,6.402972694\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.087034878,3.529499253,4.009441171,4.518873306,5.048808812,5.590529227,6.136362184\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.65665144,4.337098381,5.038487053,5.741548786,6.431948891,7.099834236,7.739066651\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.525375238,4.194877572,4.888899761,5.587750183,6.276587923,6.945056991,7.5865636\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.656908443,4.33760455,5.0391627,5.742334857,6.432800837,7.100718231,7.73995706\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.532358043,4.202563143,4.897232977,5.596625983,6.285878758,6.954632125,7.596300952\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.145407656,3.621741895,4.131422626,4.666099429,5.216677055,5.774578481,6.332458993\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,2.956854333,3.403449665,3.886537062,4.398978785,4.932166325,5.477495326,6.027274221\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.370731621,3.84005371,4.344668253,4.875074215,5.421466503,5.974876617,6.527785513\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.43243987,3.930287386,4.463126615,5.019254174,5.58770802,6.159110173,6.726010707\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.099993129,3.542044127,4.021689669,4.530881622,5.060585988,5.602051826,6.147586859\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.260251337,3.724524433,4.225528796,4.753797782,5.299445394,5.853352139,6.407812353\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,2.949062589,3.395149616,3.878000775,4.390414833,4.923725468,5.469280444,6.01935084\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.143334726,3.619231621,4.128806043,4.663615139,5.214481744,5.772764649,6.331073051\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.372804217,3.84201733,4.34652705,4.87682791,5.423113626,5.976414828,6.529211303\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.439870875,3.937395444,4.469783637,5.02539116,5.593298923,6.164156378,6.730529024\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.249598901,3.715235792,4.217441357,4.746751948,5.293290816,5.847950795,6.403039677\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.087058198,3.529500984,4.009423582,4.518839038,5.048760606,5.590469744,6.136293887\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.656494789,4.336938273,5.038325837,5.741388496,6.431791176,7.099680363,7.738917542\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.525314262,4.194808488,4.888824107,5.587669541,6.276503788,6.944970702,7.586476304\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.656803163,4.33749977,5.039059912,5.742235147,6.432704933,7.100626576,7.739869878\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.532386184,4.202592786,4.897263996,5.596658127,6.285911716,6.954665573,7.596334585\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.145412486,3.621756768,4.131445188,4.66612752,5.216708827,5.774612429,6.332493928\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,2.956673898,3.403258223,3.886335844,4.398769637,4.931951493,5.477277246,6.02705535\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.37087788,3.840214076,4.34484083,4.875256592,5.421656047,5.975070689,6.527981618\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.432432824,3.930272982,4.463105337,5.019226866,5.587675711,6.159073953,6.725971646\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.100112437,3.542156904,4.021796885,4.530984016,5.060684073,5.60214593,6.147677176\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.260413074,3.724686342,4.225690742,4.753959296,5.299605768,5.853510538,6.407967902\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,2.948972984,3.395058018,3.877908221,4.39032227,4.923633757,5.469190359,6.019263068\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.143253267,3.619145073,4.12871567,4.663522148,5.214387257,5.77266968,6.330978495\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.372779185,3.841996342,4.346509779,4.876813973,5.423102584,5.976406194,6.529204561\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.439847345,3.937373156,4.469762566,5.025371331,5.593280378,6.164139157,6.730513161\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.249620683,3.715262425,4.21747182,4.746785246,5.293325993,5.847986949,6.40307597\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,3.087043042,3.529490026,4.009416225,4.518834772,5.048758997,5.590470426,6.136296563\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.295168603,9.919296127,10.56052833,11.20851181,11.85361121,12.48760963,13.10398551\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.317279678,9.934348118,10.57136646,11.21712043,11.86129479,12.4951697,13.11187118\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.299397509,9.925796955,10.5686642,11.21779183,11.86365355,12.49811816,13.11473281\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.327103743,9.942636885,10.57816811,11.22253301,11.86544741,12.4982062,13.11393782\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.453178046,10.3107402,11.13983797,11.93258307,12.68382418,13.39073979,14.05236129\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.67345624,11.336907,11.99831347,12.64962593,13.2833028,13.89330753,14.47537833\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.843617984,10.61124032,11.36964105,12.10723773,12.81562235,13.48928638,14.12511823\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.457196431,10.31385489,11.14205855,11.93397422,12.68448171,13.3907712,14.05187309\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.69264086,11.35515977,12.0155269,12.66574791,13.2983279,13.90726363,14.48831444\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.806376195,10.57487424,11.33425604,12.07294634,12.78252155,13.45744748,14.09458473\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.29511173,9.919243363,10.56048328,11.2084764,11.85358614,12.48759475,13.10398017\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.317277002,9.934344768,10.57136419,11.21712044,11.8612978,12.49517603,13.11188085\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.299352825,9.925752583,10.56862257,11.21775434,11.86362087,12.49809047,13.11470994\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.327108694,9.942641622,10.57817348,11.22253959,11.86545554,12.498216,13.11394926\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.453110897,10.31066174,11.13975323,11.9324957,12.68373673,13.39065396,14.05227814\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.67338553,11.33682854,11.99822829,12.64953547,13.2832086,13.89321103,14.47528083\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.843580801,10.611189,11.36957787,12.10716522,12.81554294,13.48920223,14.12503118\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.457081669,10.31373166,11.14193087,11.93384512,12.68435341,13.39064525,14.05175056\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.69260927,11.35512668,12.0154924,12.6657123,13.2982916,13.90722704,14.48827789\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.806471297,10.57495539,11.33432437,12.07300333,12.78256877,13.4574864,14.0946167\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.295191112,9.919317548,10.56054987,11.20853408,11.85363442,12.48763376,13.10401043\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.317308737,9.93437459,10.57139251,11.21714751,11.86132374,12.49520089,13.11190466\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.299368462,9.92576603,10.56863076,11.2177557,11.86361486,12.49807726,13.11469013\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.327139438,9.942660102,10.5781802,11.22253555,11.86544203,12.49819441,13.11392098\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.453145139,10.31070097,11.13979456,11.93253714,12.68377701,13.39069232,14.05231421\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.67339884,11.33685441,11.99826528,12.64958181,13.28326246,13.89327065,14.47534461\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.843760087,10.61137506,11.36976865,12.10735859,12.8157369,13.48939499,14.12522125\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.457113904,10.31376167,11.14195851,11.93387039,12.68437643,13.39066622,14.05176969\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.69258116,11.35510831,12.01548215,12.66570869,13.29829333,13.90723297,14.48828708\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.80647292,10.57496681,11.33434399,12.07302953,12.7826,13.45752132,14.09465414\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.5324654,12.27774537,13.01018593,13.7205603,14.40182811,15.04917749,15.65976768\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.809519773,10.50175544,11.19479621,11.88319679,12.56042527,13.220202,13.85723846\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.30488928,12.1118057,12.90136588,13.6635921,14.39081734,15.07794346,15.7221923\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.57998347,11.30585369,12.03146077,12.74694178,13.44348052,14.11409348,14.75380508\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.50055071,12.24252387,12.9727201,13.68176292,14.36244374,15.00979043,15.62082176\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.750920605,10.445646,11.14002546,11.82904461,12.50654953,13.16652918,13.80385936\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.51098741,12.29987969,13.07436186,13.8237851,14.53994111,15.21732287,15.85285613\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.84734475,11.56307719,12.28076779,12.98934014,13.67925067,14.3431331,14.97585362\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.47584063,12.23025023,12.97009124,13.68647217,14.37262772,15.02397034,15.63784001\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.831992599,10.52814604,11.2246061,11.91580389,12.59517527,13.25646885,13.89445897\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.36993262,12.17660409,12.96535685,13.72628695,14.45182037,15.13695688,15.77901021\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.51976665,11.25236722,11.98367924,12.70404402,13.404797,14.07907045,14.72197937\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.53717007,12.27887081,13.00842078,13.71651659,14.39602699,15.04205161,15.65167029\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.702419503,10.40140492,11.09950261,11.79178575,12.472175,13.13472068,13.77434799\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.50079035,12.29065473,13.0657684,13.8156323,14.53212602,15.20979316,15.84558753\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.79648609,11.51538669,12.23569658,12.94655452,13.63854506,14.30437434,14.93894676\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.53222205,12.27751433,13.00996481,13.72034807,14.40162439,15.0489822,15.65958082\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.809508587,10.50172366,11.19474601,11.88313075,12.56034615,13.22011245,13.85714094\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.30500604,12.11194787,12.90152773,13.66376819,14.39100282,15.07813428,15.72238517\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.57997608,11.30585321,12.03146853,12.74695818,13.44350527,14.11412585,14.75384409\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.50057827,12.24254656,12.97274044,13.68178276,14.36246426,15.0098123,15.62084528\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.750902453,10.44564505,11.14003944,11.82907116,12.50658632,13.16657405,13.8039104\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.51110504,12.29996981,13.07442895,13.82383328,14.53997394,15.2173434,15.8528669\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.84733342,11.5630662,12.28075553,12.98932579,13.67923397,14.3431141,14.97583257\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.47594011,12.23034618,12.97018439,13.68656281,14.3727159,15.02405597,15.63792297\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.831982345,10.52812524,11.22457809,11.91577113,12.59513957,13.25643154,13.89442102\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.36986147,12.17653961,12.96529833,13.72623368,14.45177168,15.13691218,15.77896902\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.51990392,11.25247359,11.98376087,12.70410602,13.40484352,14.07910485,14.72200431\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.53721245,12.27893234,13.00849767,13.71660531,14.39612443,15.04215508,15.65177755\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.702458713,10.40146184,11.09957487,11.79187071,12.47226998,13.13482317,13.77445575\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.50088428,12.29075164,13.06586675,13.81573081,14.53222366,15.20988912,15.84568118\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.79648677,11.5154067,12.23573274,12.9466038,13.63860466,14.30444177,14.93901989\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.5324356,12.2777151,13.01015248,13.7205224,14.40178543,15.04913028,15.65971652\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.809485307,10.50169553,11.19471508,11.88309859,12.56031389,13.2200809,13.85711063\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.3048357,12.11179904,12.90139786,13.66365492,14.39090402,15.07804803,15.72230977\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.5801093,11.30595744,12.03154915,12.74701962,13.44355116,14.11415918,14.75386729\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.5005699,12.24252429,12.9727059,13.68173785,14.36241097,15.00975248,15.6207806\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.750961825,10.4456843,11.14006034,11.829076,12.50657756,13.1665541,13.80388145\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.51112175,12.29998984,13.074452,13.82385891,14.54000166,15.2173727,15.85289729\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.84736447,11.56311237,12.28081567,12.98939811,13.6793164,14.34320451,14.97592895\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.47587319,12.23026916,12.97010223,13.68647917,14.37263338,15.0239763,15.63784721\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.832007175,10.5281712,11.22464097,11.91584715,12.59522545,13.25652447,13.89451866\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.36992357,12.17657415,12.96530927,13.72622498,14.45174707,15.13687503,15.77892223\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.51975867,11.25233108,11.98361669,12.70395798,13.40469095,14.07894805,14.72184412\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.53722962,12.2789272,13.00847506,13.71656953,14.39607909,15.04210311,15.65172126\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,9.702269942,10.40128703,11.09941401,11.79172348,12.47213575,13.13470113,13.77434495\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,11.50093614,12.29078384,13.06588267,13.81573352,14.53221588,15.20987313,15.84565893\n\"linker C(Cn1nncn1)Cn1nncn1, nodes [Zn], topology rna\",,,10.79651265,11.51540768,12.23571063,12.94656127,13.63854475,14.30436757,14.93893434\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,19.71840669,20.14471695,20.47854433,20.74444009,20.95944071,21.13562216,21.28171498\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.675194454,4.403686031,5.143711052,5.876693029,6.589414977,7.273278727,7.923369879\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.77138257,4.487922151,5.216986922,5.940068005,6.643928326,7.319889586,7.962924104\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.93645953,4.676414026,5.419881929,6.150196089,6.855891448,7.529799638,8.168096022\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.464380233,4.168812937,4.893040153,5.617125857,6.326446946,7.011127993,7.665172638\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.93631136,4.676265611,5.419732514,6.150045982,6.855741454,7.529650725,8.167949134\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.464902027,4.169387782,4.893653138,5.617763453,6.327097504,7.011781875,7.665822141\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.675069947,4.403563172,5.143591818,5.876578865,6.589306773,7.273176894,7.923274455\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,3.77162368,4.488175348,5.217238993,5.940310672,6.644156936,7.320101969,7.963119698\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,4.016319175,4.757355042,5.500805265,6.23014453,6.934055814,7.605504811,8.240780881\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,4.031670759,4.781219854,5.533040642,6.269916853,6.980189327,7.656718032,8.295830357\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,4.017042257,4.758095767,5.501547386,6.230876137,6.934768586,7.606193231,8.241441546\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,4.03120976,4.780709679,5.532497188,6.269353622,6.979617281,7.656145768,8.295264415\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.846560384,9.550077684,10.24996637,10.93981378,11.61360514,12.266241,12.89376379\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,9.115268679,9.797694666,10.48256838,11.16154566,11.82711838,12.47311575,13.0948587\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.946973213,9.641637437,10.33288073,11.0143894,11.68029511,12.32561929,12.9464768\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,9.209723245,9.892511447,10.57642605,11.25353586,11.91662195,12.55971834,13.17829461\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.946317649,9.641096831,10.33243366,11.01401845,11.67998616,12.32536088,12.94625967\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,9.208662487,9.891531954,10.57552723,11.25271443,11.91587314,12.55903669,13.17767444\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.845955562,9.549518874,10.24944662,10.93932851,11.61315114,12.26581581,12.89336536\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,9.113468951,9.796022774,10.48100628,11.16007986,11.82573864,12.47181409,13.09362872\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.941307746,9.624819244,10.30834308,10.9848975,11.64798356,12.29207551,12.9128396\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,9.271274464,9.957996102,10.64638668,11.32811756,11.99566017,12.64281617,13.26489721\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.941672519,9.625191766,10.30872188,10.98528078,11.64836923,12.29246138,12.91322355\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,9.271501628,9.958160055,10.64650108,11.32819332,11.99570591,12.6428387,13.26490186\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.11770319,10.91519037,11.69792028,12.45698632,13.18534374,13.87806416,14.53217449\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.90901743,11.66275376,12.40229849,13.11887334,13.80580814,14.45859062,15.07459925\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.86368197,9.576004281,10.28434975,10.98515141,11.67341036,12.34392462,12.99206427\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,12.04321538,12.77266174,13.47091252,14.13646258,14.76779443,15.36382072,15.92407021\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.11735608,10.90382355,11.67748161,12.42937135,13.15228002,13.84104972,14.49246053\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.92502322,11.66684344,12.39682534,13.1059935,13.78739541,14.43620813,15.04950987\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.92389338,9.634508977,10.3412665,11.04050221,11.72715893,12.39600823,13.04241658\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,12.16378822,12.90292018,13.60858445,14.2793618,14.91391654,15.5114027,16.07161641\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.11779173,10.9042241,11.67785337,12.42971873,13.15260613,13.84135684,14.49275039\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.92398675,11.66590967,12.39597908,13.10522249,13.78668969,14.43555953,15.04891163\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.923439096,9.634058447,10.34081748,11.04005437,11.72671318,12.39556617,13.04198007\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,12.16565489,12.90432079,13.6096282,14.2801317,14.9144758,15.51179963,16.07188803\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.11659948,10.91422197,11.69706852,12.4562352,13.18467949,13.87747497,14.53165023\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.90986258,11.6635819,12.40310055,13.11964365,13.80654339,14.45928921,15.0752608\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.864156912,9.576422682,10.28471453,10.98546741,11.67368315,12.34415976,12.99226694\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,12.04567782,12.774854,13.47288339,14.13824823,14.76942233,15.36531227,15.92544249\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.15312641,10.93280641,11.70159084,12.45031522,13.17142036,13.85938087,14.51065074\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.8948794,11.62676238,12.35191152,13.06025039,13.74370427,14.39645739,15.01478937\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.804848646,9.519682002,10.23011204,10.93243672,11.62172794,12.29292727,12.94155219\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,12.28256042,13.0351682,13.75409289,14.43678986,15.08126866,15.686408,16.25199521\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.15318165,10.93281226,11.70155882,12.45025483,13.17133928,13.85928519,14.51054522\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,10.89555662,11.62738379,12.35248088,13.06077168,13.74418157,14.39689469,15.01519047\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,8.804624711,9.519450227,10.22987114,10.93218744,11.62147212,12.29266719,12.94129019\n\"linker n1ncn(c1)[N][N]n1cnnc1, nodes [Fe], topology ths,acs\",,,12.27837952,13.03135313,13.75058351,14.43354382,15.07825473,15.68360198,16.24937746\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,17.38445687,18.13514807,18.75149478,19.26155952,19.68707187,20.04485101,20.34795952\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,17.36662036,18.11933771,18.73745793,19.24906111,19.67590348,20.03483235,20.33893651\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,19.30403971,19.83701635,20.26282366,20.60759824,20.89018161,21.12436744,21.32040419\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,1.967365894,2.458205761,3.006677066,3.601129895,4.229900084,4.882221047,5.548628178\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,3.327576231,3.996013835,4.684551264,5.376390471,6.058433942,6.721274803,7.358758321\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,1.951197187,2.43862955,2.984222631,3.576552689,4.204065065,4.856000594,5.522827386\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,3.323030817,3.990666906,4.678520237,5.369810726,6.05144232,6.713999047,7.351311371\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,1.962464502,2.452358948,2.999985641,3.593774487,4.222109162,4.874239867,5.540693942\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,3.325058039,3.993372758,4.681850848,5.373681895,6.055756326,6.71865662,7.356219235\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,1.9498532,2.437297761,2.983060587,3.575693422,4.203609561,4.856016439,5.523351438\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,3.323273463,3.990966024,4.678887304,5.370247092,6.051942916,6.714555242,7.35191299\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,9.181913278,10.0133348,10.80843607,11.5657317,12.2843501,12.96396991,13.60477712\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.406509901,8.242835124,9.063854785,9.865214387,10.64259411,11.39212416,12.11066957\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.311339394,8.153265907,8.980732427,9.788651852,10.57231282,11.32766118,12.05149681\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.646183839,7.470584053,8.283848629,9.080068555,9.854675221,10.60401224,11.3251885\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.719221758,7.519728339,8.314253426,9.095749445,9.858658507,10.59854183,11.31192821\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,9.178429609,10.00962647,10.80453798,11.56168665,12.28020241,12.9597618,13.60054676\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.429524346,8.263222705,9.081629868,9.880527554,10.65566469,11.40319773,12.11999254\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.278771591,8.124863062,8.956150804,9.76748354,10.55413989,11.31208587,12.03815653\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.660754783,7.483008814,8.294443464,9.089146074,9.862522324,10.61087764,11.33127876\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.71569616,7.519430734,8.316250392,9.099347935,9.863342121,10.6039271,11.31773253\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,9.178614376,10.0095779,10.80428145,11.56123722,12.27957402,12.95897036,13.59961041\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.407204491,8.242990952,9.063443232,9.864245557,10.64110544,11.39017008,12.10831307\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.307340037,8.149716207,8.977640635,9.786000701,10.57007027,11.32578786,12.04995095\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.64427448,7.468851657,8.282190671,9.078422028,9.853004393,10.60229989,11.32342961\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.723388487,7.523973855,8.318535801,9.100019065,9.862867403,10.60264849,11.31589955\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,9.179798993,10.01071241,10.80541157,11.56239735,12.28078581,12.96024433,13.60094852\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.432771187,8.265925706,9.08384648,9.882313009,10.65707189,11.40427653,12.12078906\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,7.278640315,8.124337123,8.955312276,9.766396486,10.55285644,11.31064958,12.03660421\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.657483173,7.480272133,8.292158131,9.087237407,9.860925541,10.6095378,11.33015003\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,6.721062261,7.523354364,8.319052628,9.101268371,9.864564364,10.60459468,11.31795932\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.74341735,14.61789689,15.40616356,16.11726648,16.75939326,17.3398698,17.86522181\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,14.79799008,15.54681416,16.21297938,16.80958517,17.34702806,17.83357533,18.27585001\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.7728664,14.66072797,15.45877514,16.17671142,16.82330682,17.40638661,17.93289485\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,15.38861333,16.0362531,16.62393476,17.1590214,17.64763729,18.09489243,18.50509007\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.85383693,14.7185211,15.49818274,16.20167378,16.83702844,17.41145127,17.93137035\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,14.79225095,15.53687724,16.20125434,16.79746894,17.33530497,17.82265938,18.26593256\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.82267105,14.70280086,15.49455038,16.20736877,16.84979682,17.42946735,17.95316868\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,14.94316273,15.64653364,16.28025862,16.85378095,17.37478538,17.84957088,18.28335768\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.73560764,14.61179442,15.40130436,16.113327,16.75614529,17.33715025,17.86291248\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,14.76534376,15.51775375,16.18696428,16.78617019,17.32584646,17.81432417,18.25827791\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.77495235,14.66238635,15.4601044,16.17779364,16.82420669,17.40715317,17.93356423\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,15.42259575,16.06396445,16.64687499,17.17824831,17.66391891,18.10880072,18.51706045\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.89409806,14.75372221,15.52912215,16.22900813,16.86129919,17.43310626,17.95078122\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,14.76567834,15.51287762,16.17944474,16.77754882,17.31703334,17.80583923,18.25040008\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,13.83645005,14.71455639,15.5047394,16.21631002,16.85771976,17.43654263,17.95952713\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,15.04846708,15.7387182,16.36168395,16.9262619,17.43974109,17.90812812,18.33642344\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,15.06308722,16.01413984,16.81462329,17.4939509,18.07572897,18.57860434,19.01721305\n\"linker [O-]C(=O)c1cc(C(=O)[O-])c(cc1C(=O)[O-])C(=O)[O-], nodes [Ni][OH2][Ni][OH2][Ni], topology scu,pcu\",,,15.06310702,16.01390282,16.8142232,17.49346124,18.07520696,18.57809386,19.01674699\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,16.44622288,17.15642727,17.78306037,18.33532844,18.82184605,19.25059286,19.62882862\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,18.91119797,19.39179594,19.80958291,20.17370987,20.49179548,20.77031398,21.0148039\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,15.98819773,16.74146898,17.40854192,17.99762092,18.51708113,18.97504388,19.3790799\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,17.09820716,17.77717239,18.36794561,18.88253572,19.33145909,19.72388905,20.0677705\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,20.2211574,20.67982289,21.04278321,21.33435464,21.57176285,21.76742746,21.93045544\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,18.78956182,19.39909944,19.89807562,20.30997648,20.65285992,20.94062611,21.18402222\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.1711085,3.790880617,4.439584794,5.100554302,5.760065618,6.40771483,7.036227685\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.383256918,4.04169178,4.722557094,5.408437448,6.085810059,6.744994756,7.379667454\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.526154312,4.189453388,4.872854588,5.559288461,6.235598136,6.892449531,7.5238261\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.38507709,4.003473828,4.643928737,5.291920169,5.935609734,6.566052138,7.177000963\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.970486954,4.53423853,5.12430794,5.727164251,6.331090383,6.926851893,7.507757115\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.323086689,3.926329734,4.55576468,5.196433833,5.835916794,6.464684207,7.075970244\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.665755729,4.326363832,5.004699634,5.684381085,6.352882001,7.001371409,7.624198016\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.473528424,4.142785844,4.831985783,5.523857657,6.20512372,6.86639666,7.501654985\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.47169439,4.099227502,4.747802739,5.402594502,6.051627437,6.685960536,7.299451401\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.973071976,4.537290062,5.127864035,5.731144672,6.335376191,6.931325747,7.512320776\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.42923391,4.057263735,4.707784441,5.365537735,6.018163916,6.656421817,7.273955706\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.496239613,4.16066311,4.845151281,5.532572285,6.209765167,6.867415811,7.49953261\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.489096199,4.151657437,4.83505489,5.522039625,6.199298299,6.857368696,7.490133917\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.371726847,3.989869685,4.630478839,5.278957454,5.923392022,6.554775298,7.166815536\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.99490018,4.560051606,5.150923542,5.754084441,6.357921693,6.953296774,7.533599538\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.381711778,3.989072916,4.621442999,5.263948585,5.904302814,6.533127897,7.14380797\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.672744322,4.33868966,5.022351166,5.706976919,6.379821177,7.031954729,7.657713742\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.510257129,4.179219781,4.86789959,5.559025089,6.239342792,6.89950279,7.533525053\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.325343593,3.949725503,4.597745356,5.254135336,5.906440391,6.545282297,7.164154294\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,3.946238747,4.5040169,5.08897013,5.687554735,6.288052516,6.881213118,7.460307862\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.281642398,10.03367509,10.76668125,11.47705184,12.16144147,12.81712122,13.44213234\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.726099805,10.46395353,11.18104528,11.8740445,12.54000831,13.17665668,13.78245964\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,7.942640883,8.688970488,9.428192138,10.15692325,10.87112358,11.56664732,12.2397142\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.696490596,10.43878609,11.15761039,11.85035104,12.51478378,13.14921816,13.75255684\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.216284396,9.96716047,10.70008445,11.41101326,12.09635629,12.75324352,13.37963085\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,10.09679353,10.82093638,11.51916025,12.19000683,12.83217218,13.44465738,14.02685162\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.332792557,10.05793763,10.76923994,11.46202216,12.13216787,12.77637368,13.39223299\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.820629216,10.53167161,11.22690845,11.90197537,12.55318825,13.17771827,13.77361027\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,7.914428419,8.656268328,9.39003294,10.112971,10.82154219,11.5119441,12.18059799\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.561200868,10.31848136,11.04998954,11.75365891,12.4276132,13.07039956,13.6810956\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.24839558,9.986188045,10.70767042,11.40888324,12.08618801,12.73658977,13.35787907\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,10.14389864,10.85016513,11.53309582,12.19092855,12.82211366,13.42543518,14.00008015\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.258907805,10.01196132,10.74782217,11.46190319,12.15023857,12.80973178,13.43822528\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.74172348,10.48040239,11.19876101,11.8931117,12.56031691,13.19800268,13.804605\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,7.930242172,8.678873975,9.420871595,10.15255873,10.86967968,11.56794523,12.24349028\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.707350853,10.45202769,11.17341223,11.86864116,12.5353368,13.1717252,13.7766744\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.241492602,9.99315243,10.7266015,11.43778626,12.12313448,12.7798088,13.40580322\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,10.08216985,10.80882075,11.50915141,12.18176189,12.8253993,13.43910938,14.02232009\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.358482265,10.08187008,10.79231323,11.48476213,12.15484519,12.79909241,13.41499464\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.842257415,10.55159543,11.24543173,11.91934747,12.56960967,13.19334546,13.7885618\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,7.940466556,8.681737424,9.415152425,10.13779904,10.84604949,11.53606043,12.20424043\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.605745751,10.35559265,11.08078231,11.77910202,12.44854147,13.08752945,13.69503989\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.148624848,9.901550809,10.63533068,11.34659839,12.03217074,12.68940599,13.31637227\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,10.17066184,10.87161394,11.55021643,12.20449541,12.83274765,13.43364358,14.00628382\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.520734428,10.3898186,11.22611255,12.02631627,12.7876275,13.50809062,14.18670047\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,10.02682205,10.85730923,11.65595197,12.42032657,13.14813069,13.83764975,14.4879422\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,9.510359544,10.38278595,11.2224269,12.02573242,12.78977383,13.51255029,14.19306059\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,10.09807461,10.91946137,11.71019214,12.46783225,13.18996455,13.87472456,14.52102053\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,17.33638105,17.98991959,18.57572584,19.10106278,19.57182285,19.99333314,20.37058726\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,17.02847331,17.75319619,18.3945381,18.96294477,19.46701484,19.91426955,20.31143323\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,16.15737685,17.1093923,17.92948692,18.63601622,19.24562391,19.77291317,20.23043034\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,14.80100726,15.84509727,16.75578356,17.5492895,18.24093279,18.84461817,19.37264412\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,15.20817074,16.36338538,17.34159254,18.1703942,18.87452185,19.47509929,19.98972819\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,16.93264472,17.63986573,18.26902469,18.82992538,19.3302847,19.77674566,20.17526394\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,16.55956685,17.32370128,18.0000455,18.59986729,19.13231588,19.60529583,20.02581942\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,16.02855481,17.01757678,17.86849583,18.59942481,19.22774729,19.76907848,20.23694494\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,14.69243032,15.75637543,16.68336536,17.49008495,18.19236879,18.80460462,19.33950647\n\"linker n1ccc(cc1)C=Cc1ccncc1, nodes [Co], [O], [V], topology \",,,16.16892887,17.13464163,17.96781912,18.68490974,19.302203,19.83457885,20.29505746\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,20.41348763,20.66410866,20.86244613,21.02185356,21.15173955,21.25887116,21.34820585\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,20.80136991,21.0572882,21.25939327,21.42155464,21.55350501,21.66222013,21.752795\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,20.52452406,20.75771127,20.94086949,21.08715537,21.20572646,21.30309765,21.38399573\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,20.87642919,21.13019404,21.32984484,21.48953848,21.61914337,21.72569247,21.81429788\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.388188299,4.045848854,4.726090705,5.411709726,6.089181305,6.748727217,7.383898357\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.358756939,4.010734901,4.687707547,5.372004017,6.049575523,6.71016545,7.346933463\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.375782016,4.034992663,4.717458866,5.405599088,6.085610601,6.747537848,7.384834645\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.387916111,4.039308888,4.714817019,5.397147322,6.072546538,6.730972873,7.365732283\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.450971188,4.11805611,4.806187015,5.497975348,6.179911176,6.842356657,7.479067026\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.341754381,3.992030076,4.666922682,5.3489757,6.024343449,6.682922319,7.317967495\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.425178931,4.085500967,4.767802796,5.454869755,6.133176046,6.792970651,7.427858231\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.292999133,3.943905194,4.620979719,5.306261094,5.985442254,6.648056072,7.287099899\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.445778773,4.104249728,4.783608519,5.467029531,6.141367995,6.797179148,7.428282612\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.477620727,4.136358848,4.816961939,5.502251912,6.178767266,6.836816504,7.4700478\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.425867693,4.083462738,4.76399925,5.450040868,6.127886351,6.78764669,7.422818253\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,3.433216464,4.088481262,4.76664693,5.450398199,6.12611395,6.78393983,7.417370996\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.494496001,8.315577033,9.121643287,9.90868173,10.67289429,11.41083603,12.11961778\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.317796677,10.10312932,10.86535771,11.6003108,12.30453787,12.97557133,13.61193676\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.805052742,8.590837404,9.3618639,10.11577373,10.84962345,11.560327,12.24505282\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.348127564,10.1173455,10.8668609,11.59191848,12.28855256,12.95385481,13.58598164\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.671595704,8.467177536,9.249588609,10.01548482,10.76122132,11.48324796,12.17845349\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.428452995,10.20900577,10.96460855,11.69222217,12.38903546,13.05292141,13.68257049\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.761919527,7.57033281,8.373711349,9.164057511,9.935153893,10.6822223,11.40169677\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.817279048,7.583788898,8.346863856,9.10176024,9.843882785,10.56887175,11.27280792\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.58243149,7.385657587,8.181901443,8.96529235,9.731054002,10.47516033,11.19426\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.779656107,8.569924867,9.344518076,10.1012441,10.83733111,11.54984581,12.2360814\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.336605194,10.11542317,10.87254262,11.60365049,12.30512174,12.97431057,13.60957649\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.695120182,8.502315777,9.296847208,10.07438344,10.8307114,11.56199829,12.26503908\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.431893002,10.22822627,10.99948573,11.74169431,12.45155208,13.12673457,13.76591689\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.727992219,8.5360187,9.329308825,10.10433639,10.85747421,11.58528988,12.28483666\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.342261801,10.11919194,10.87534545,11.605948,12.30711295,12.97605444,13.61106253\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.903659535,7.646195226,8.39089689,9.131604725,9.862704448,10.57909469,11.27630903\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.729321276,7.486058181,8.246580228,9.003647324,9.750806663,10.48236845,11.19349766\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.863520541,7.671418246,8.474791977,9.265438681,10.03690052,10.78420978,11.50368207\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.595679396,8.397978932,9.186119302,9.956674681,10.70605231,11.4308184,12.12799988\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.25326587,10.03974849,10.80226403,11.53692131,12.24046449,12.91056633,13.54585508\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.635022662,8.419290969,9.187153177,9.937023043,10.66656293,11.37312075,12.054147\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.294443693,10.05974656,10.80447344,11.52445469,12.21618487,12.87707158,13.50545825\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.702237908,8.491861663,9.264618759,10.01879196,10.75201861,11.46165936,12.14519143\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.253502438,10.04253826,10.80824556,11.54612389,12.25255425,12.92502057,13.56207824\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.271459555,7.037525395,7.802616043,8.560791705,9.306767269,10.03580419,10.74378538\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.231054264,6.981123198,7.729309853,8.470682304,9.200628606,9.914808973,10.60930284\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.701638388,7.48683747,8.267458894,9.037388197,9.791371169,10.52492463,11.23435415\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.795502248,8.575767537,9.342438115,10.09299846,10.82436509,11.53332102,12.21691301\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.433795327,10.20457678,10.95423852,11.6783375,12.37319297,13.03614255,13.66554501\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.623071088,8.426617504,9.216041796,9.987870972,10.7385285,11.46461212,12.16317497\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.421555165,10.19093925,10.93863611,11.6607265,12.35380155,13.0153146,13.64365091\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.852520408,8.639684943,9.412076596,10.16715923,10.90191111,11.61321705,12.29824284\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,9.318957342,10.09600891,10.85351229,11.58600983,12.28920884,12.96009675,13.59684877\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.856767996,7.594877497,8.336911784,9.076555214,9.807917009,10.52558206,11.22478506\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,6.549862021,7.33829617,8.121696827,8.894583168,9.652213432,10.39040752,11.10556897\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,7.079257905,7.905420556,8.720428478,9.515799365,10.28565527,11.02608453,11.73463181\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,12.82749511,13.72591037,14.5642239,15.34100547,16.05633264,16.7118318,17.31033158\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.98274809,15.72574594,16.38224758,16.96721513,17.4922624,17.96645273,18.39692048\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.20033909,15.05516431,15.81715352,16.4999283,17.11430906,17.66903792,18.17130735\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.04272189,14.91637341,15.69163089,16.38394198,17.00540416,17.56563422,18.0724108\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.88682371,15.67981873,16.37956301,17.00236687,17.56058958,18.0637493,18.51931474\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,13.91585865,14.77983318,15.55566618,16.25406606,16.88427502,17.45422394,17.97072362\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,15.10685315,15.83618802,16.49709813,17.09722986,17.64306296,18.14016674,18.59339489\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,15.45861688,16.16454971,16.79620682,17.3652135,17.88041907,18.34873275,18.77569007\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,15.87792553,16.535193,17.12269058,17.65207669,18.13191746,18.56871502,18.96757078\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.3099952,15.14955573,15.90164018,16.5774479,17.1863368,17.73620203,18.23377346\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.56977059,15.37541237,16.08349039,16.71128634,17.27224377,17.77685661,18.23337025\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,13.38938417,14.22866478,15.01913311,15.7563982,16.43844528,17.06542949,17.63913999\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.49189673,15.57413246,16.51748743,17.33920659,18.05551577,18.68101954,19.22853077\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.87253308,15.93695421,16.8578957,17.65500286,18.34603194,18.94655172,19.46996378\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.30938573,15.13638274,15.87039941,16.52656104,17.11641123,17.64895767,18.13140118\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,12.88283039,13.53475715,14.12604182,14.66418497,15.15532673,15.60454841,16.01612112\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,10.65468607,11.26479556,11.81905636,12.32491084,12.78808584,13.2131385,13.60381697\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,13.47430953,14.36837281,15.17055849,15.89215935,16.54280966,17.13074645,17.66304857\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,13.36368062,14.14944797,14.89544983,15.59618556,16.24854804,16.85165152,17.40633177\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,13.48052775,14.38279082,15.18369203,15.89769846,16.53712799,17.11228333,17.63171514\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.87044131,15.63767029,16.3296226,16.95540663,17.52261087,18.03765938,18.50607077\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.9316375,15.70839573,16.40221038,17.0253655,17.58748856,18.09629502,18.55810383\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.9535557,15.74130054,16.43444305,17.05054358,17.60256495,18.10027946,18.55122484\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,13.86108654,14.73308666,15.51631574,16.22155294,16.85805073,17.43374423,17.95545943\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,15.83170224,16.46932539,17.03159345,17.53247447,17.98276829,18.3908225,18.7630945\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,12.4849353,13.46205989,14.36728544,15.20000237,15.96146236,16.65459603,17.28352081\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,14.99931894,16.06123279,16.97911759,17.77340147,18.46215345,19.06101156,19.58333348\n\"linker [O]OC(=O)c1cc(cc(c1)C(=O)[O-])C(=O)[O-], nodes [In], topology \",,,15.92203798,16.8806739,17.70445226,18.4150189,19.03025104,19.56495759,20.03144007\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,21.09612335,21.42965792,21.69347703,21.90540142,22.07799018,22.22027384,22.33886519\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,21.27784415,21.582645,21.82389501,22.01780494,22.17580717,22.30612788,22.41479491\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,21.00644214,21.35413022,21.62908074,21.84989603,22.02968624,22.17787701,22.30136914\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,21.09489087,21.42862144,21.6925943,21.90464126,22.07732913,22.219694,22.33835266\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,21.28023065,21.58466128,21.82561852,22.01929354,22.17710478,22.30726835,22.41580469\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,21.00705791,21.35464926,21.62952348,21.85027773,22.03001842,22.17816854,22.30162694\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,3.345870824,4.040656281,4.751459993,5.461160727,6.156873848,6.829667081,7.473953386\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,3.342516642,4.037079184,4.747801503,5.457523294,6.153326983,6.826254888,7.470701414\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,3.347026124,4.041891987,4.752779863,5.462552762,6.158319943,6.831148152,7.475451857\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,3.345914913,4.040700276,4.751503316,5.461202952,6.156914681,6.829706335,7.473990955\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,3.342484029,4.037046455,4.747768929,5.457491106,6.153295376,6.826224022,7.470671412\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,3.347012163,4.041878345,4.752766634,5.462540023,6.158307745,6.831136524,7.475440808\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,6.640319598,7.429535839,8.216946914,8.996004935,9.76093548,10.5066733,11.22894322\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.749129772,8.551444881,9.344514219,10.12321023,10.88229806,11.61704235,12.32356607\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.331313266,8.195394193,9.04025726,9.861846344,10.65638232,11.42052211,12.15156944\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,9.209326307,10.03621583,10.82914475,11.58571278,12.30453002,12.98498282,13.62708667\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,6.649763512,7.437171508,8.22310846,9.000969286,9.764929517,10.50988155,11.23151511\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.748077789,8.549463838,9.341767416,10.11987104,10.87852418,11.61296732,12.31929849\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.334662987,8.198976225,9.043867001,9.865379061,10.65978647,11.42377445,12.15466176\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,9.201896448,10.02786666,10.82025823,11.57658868,12.29538953,12.97598153,13.61832906\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,6.642930055,7.433010664,8.220854583,9.000075436,9.765002635,10.51063747,11.23274734\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.749210664,8.551627114,9.344781014,10.12354059,10.88267205,11.61744323,12.32398069\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.327305008,8.19147244,9.036502836,9.858300477,10.65306184,11.41742919,12.14869767\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,9.211947707,10.03849247,10.83112082,11.58741483,12.30597996,12.98620242,13.62809833\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,6.640358487,7.429581808,8.21699748,8.996058314,9.76099037,10.50672874,11.2289985\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.749130401,8.551441259,9.344507156,10.12320041,10.88228606,11.6170287,12.3235512\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.331298343,8.195381692,9.040247127,9.861838365,10.65637621,11.42051757,12.15156618\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,9.209331615,10.03621862,10.82914666,11.58571487,12.30453294,12.98498694,13.62709214\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,6.649740435,7.437152676,8.223091563,9.000952598,9.764911849,10.50986217,11.23149364\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.748111569,8.549493088,9.341791494,10.11988985,10.87853794,11.61297645,12.31930351\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.334692871,8.199011101,9.043904647,9.865417866,10.6598253,11.42381252,12.15469857\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,9.201877386,10.02784773,10.82023915,11.57656936,12.29536998,12.97596182,13.61830927\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,6.64291803,7.43300141,8.220847959,9.000071021,9.764999928,10.51063599,11.23274668\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.749203687,8.551623393,9.344779118,10.1235396,10.88267138,11.61744253,12.32397975\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,7.327271234,8.191440298,9.036472156,9.8582711,10.65303364,11.41740209,12.1486716\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,9.211935166,10.03848208,10.83111132,11.58740538,12.30597007,12.98619185,13.62808699\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.7196144,15.49676504,16.19542992,16.82533671,17.39481702,17.91095644,18.3797866\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.68739477,15.4851866,16.20121945,16.84619716,17.42880891,17.95626404,18.43466374\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.01248108,15.03236248,15.92852313,16.71731077,17.41322542,18.02883733,18.57493143\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.74484864,15.51759849,16.21299766,16.84042677,17.40798562,17.92260299,18.390203\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.8266255,15.60906558,16.31167127,16.94497235,17.5174477,18.03609802,18.50683387\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,13.77994759,14.8242789,15.74212529,16.54998802,17.26261663,17.89285741,18.45176359\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.72060445,15.49983572,16.19974132,16.83032954,17.40012488,17.91634323,18.38510345\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.49039725,15.31185288,16.04782482,16.70971602,17.30676628,17.84662095,18.33572893\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.11251036,15.12488333,16.01346442,16.79500216,17.48418516,18.09365234,18.63419229\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.72043906,15.49752992,16.19613547,16.82598555,17.39541292,17.91150364,18.38028941\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.68561337,15.48357388,16.19975543,16.84486467,17.42759309,17.95515194,18.43364405\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.01257505,15.03243816,15.92858546,16.71736323,17.41327046,18.02887667,18.57496631\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.74516374,15.51784802,16.2131929,16.84057672,17.40809769,17.9226834,18.39025705\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.82600874,15.60853498,16.31121685,16.94458443,17.51711729,18.03581703,18.50659514\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,13.77740186,14.82198077,15.74004999,16.54811118,17.26091564,17.89131191,18.45035554\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.72064979,15.49986626,16.19975971,16.83033781,17.40012469,17.916336,18.38509038\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.49116501,15.3125097,16.04839472,16.71021663,17.30721074,17.84701916,18.3360885\n\"linker [O-]C(=O)c1cc([O])c(cc1[O])C(=O)[O-], nodes [Zn], topology dmd\",,,14.11292553,15.12525354,16.01379414,16.79529601,17.48444751,18.09388715,18.63440309\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.93759854,22.28269056,22.55331557,22.7690674,22.94361495,23.0866879,23.2053426\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.99467727,22.33655373,22.60460907,22.81834232,22.99131576,23.13316378,23.25086453\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.87006166,22.1800607,22.42290931,22.61637113,22.77280057,22.90097198,23.00723813\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.12385133,21.48173569,21.7624841,21.98642252,22.16770678,22.31640271,22.43980645\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.86662353,22.21691787,22.49153221,22.71040802,22.88744641,23.03253664,23.15284753\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.11529984,21.44631312,21.70577348,21.91260871,22.07997338,22.21720645,22.33106881\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.80537649,22.11102636,22.35041155,22.54107996,22.69522926,22.82151874,22.9262157\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.11435525,21.47448504,21.7569041,21.98211668,22.16439369,22.31387758,22.43791694\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.70359979,22.06305936,22.34493785,22.56966604,22.7514903,22.90054687,23.02418412\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.22618848,21.53289489,21.77328653,21.96488247,22.11987524,22.24692782,22.3523142\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,21.71325251,22.09118591,22.38769486,22.62421729,22.81569284,22.97274884,23.10309028\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,22.02090161,22.34529212,22.59970259,22.8026116,22.96687132,23.10161202,23.21344719\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.68458871,5.093304564,5.541087714,6.018526209,6.515337564,7.02200572,7.530574795\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.598005658,4.984511544,5.413223953,5.874781375,6.358825689,6.855647139,7.357012621\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.092572186,5.50188837,5.937139521,6.391911346,6.859037166,7.33170562,7.804078396\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.313025127,5.714571572,6.139944885,6.583727036,7.039507298,7.501004411,7.962726618\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.777602607,6.182478937,6.606832259,7.045746089,7.493492714,7.944511001,8.393987946\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.706151021,5.109891867,5.549388315,6.016455061,6.50188292,6.996988165,7.494396417\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.659885574,5.074548665,5.522587695,5.996378476,6.487158298,6.986585499,7.487541809\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.950619566,6.341105806,6.754009193,7.183526195,7.623366715,8.067608203,8.511200268\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.19683661,5.595004309,6.021797088,6.470164011,6.932499314,7.401674629,7.871613199\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.416557407,5.795363191,6.203480931,6.634167163,7.0800584,7.534168558,7.990473338\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.654237301,5.061712025,5.508508151,5.985165193,6.481360807,6.987546428,7.495739787\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.605454879,4.997319894,5.43022544,5.895059747,6.381659844,6.880468324,7.383371396\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.096745823,5.509003634,5.946736521,6.403595325,6.872479318,7.346637505,7.820283164\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.31432608,5.719251155,6.147160501,6.592824159,7.049984078,7.512481762,7.974922365\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.779090836,6.185803759,6.611650768,7.051813712,7.500623821,7.952557459,8.402827173\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.723045265,5.12937739,5.570686034,6.038995101,6.525258698,7.020915001,7.518678024\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.671721158,5.086449519,5.534453489,6.008130436,6.498739288,6.997957221,7.498681108\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.856888038,6.245162885,6.656449402,7.084803301,7.523829663,7.96752498,8.410775229\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.172624789,5.569670355,5.995813281,6.443858189,6.906096912,7.375328445,7.845424491\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.346157898,5.723492821,6.130386764,6.55998563,7.004870069,7.458028014,7.913424959\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.687314933,5.094489702,5.541084566,6.0175931,6.513664438,7.019733396,7.527808816\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.595882505,4.981826697,5.410046744,5.871185392,6.354882729,6.851423766,7.352568381\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.071086734,5.481219569,5.917148105,6.372495624,6.840119725,7.313224731,7.785982658\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.293814432,5.696093969,6.121904543,6.565899507,7.021723731,7.483140013,7.944691694\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.723322063,6.128879265,6.553871274,6.993393938,7.441722937,7.893296547,8.343299781\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.726501418,5.130405338,5.569948381,6.037004583,6.522410422,7.017512802,7.514954982\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.66408551,5.077702524,5.524898535,5.998003861,6.488221949,6.987185574,7.487756871\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.595899455,5.986262363,6.399091658,6.828575576,7.268415299,7.71268019,8.156312922\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.099926877,5.498696092,5.925981212,6.374758399,6.83743673,7.306897411,7.777071029\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.048983062,5.427650692,5.835673733,6.266303352,6.712170125,7.16628233,7.622610669\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.654053032,5.060829831,5.507037505,5.983200545,6.47898363,6.98482674,7.492737415\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.376026016,4.767439198,5.199991039,5.664561153,6.150974349,6.649660642,7.152494567\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.093137625,5.505687183,5.943681143,6.400772482,6.869861593,7.344198358,7.817997122\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.313590822,5.718799263,6.146973377,6.59288371,7.050272788,7.512982993,7.975620632\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.783099538,6.189898596,6.61579579,7.055981509,7.504792406,7.956708814,8.406946522\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.716332498,5.122679288,5.56402291,6.032376176,6.518685868,7.014385537,7.512186518\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,4.66724659,5.081832099,5.529724966,6.00331647,6.493859541,6.99302626,7.4937095\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.700683519,6.089046804,6.500428632,6.928895012,7.3680538,7.811899639,8.255314245\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.12604736,5.523125023,5.949292155,6.397334876,6.859539856,7.328706956,7.798711292\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,5.08688144,5.464348327,5.871299746,6.3009061,6.745767751,7.198887675,7.654242409\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,10.03856881,10.5326389,11.03897562,11.55549548,12.07792018,12.60116472,13.12019597\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.849774604,10.32697203,10.81999255,11.32602858,11.84024455,12.35710653,12.87121457\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.336135133,8.000980335,8.670791871,9.343151874,10.01404566,10.67867011,11.33214277\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.60934593,13.17998166,13.73435366,14.2677804,14.77658588,15.25836805,15.71193284\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.811477407,10.31315209,10.82744521,11.35173215,11.88140726,12.41121734,12.93606944\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.809209467,10.33262555,10.86326237,11.40000581,11.93934301,12.47679971,13.00783305\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.416555138,8.099753142,8.784310784,9.468145209,10.1476103,10.81830092,11.47573831\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,13.20885104,13.78660253,14.34479744,14.87982829,15.38873585,15.86960917,16.32159684\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.530109132,10.01585933,10.5155822,11.02681503,11.54501098,12.06488303,12.58123969\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,10.021223,10.5159928,11.02180915,11.53714261,12.05810273,12.57984872,13.09748654\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.271374846,7.961279047,8.650766355,9.338654636,10.02184315,10.69622249,11.35744629\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.71313796,13.29509606,13.85792012,14.39795316,14.91212607,15.39840434,15.85582301\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.85902875,10.36269121,10.87784925,11.40237712,11.93201522,12.4617345,12.98657494\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.8111158,10.34110937,10.87685056,11.41754898,11.95994163,12.49974745,13.03257329\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.296928186,7.976859817,8.65891035,9.340838439,10.01887218,10.68850559,11.34517897\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.88965797,13.46363691,14.01907237,14.55205068,15.05940763,15.53909255,15.99015714\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.779380377,10.27028368,10.77442251,11.28928677,11.81037453,12.33248561,12.85052796\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.973006773,10.44797401,10.93876638,11.44267918,11.9549325,12.47001772,12.98254102\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.287872648,7.954660357,8.62615981,9.299944168,9.972015935,10.63760048,11.29184696\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.43939236,13.01152116,13.56700338,14.1012756,14.6107376,15.09303773,15.54701654\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.916454253,10.41379631,10.92380872,11.44406896,11.97011542,12.49677582,13.01898502\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.825507043,10.3438049,10.87050495,11.40421839,11.94122595,12.47689599,13.00656451\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.376890629,8.056975574,8.739069008,9.420948004,10.09886417,10.7683344,11.4248185\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.94405613,13.51946672,14.07584461,14.60946041,15.1172609,15.59726319,16.04856116\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.617661677,10.10054052,10.59808135,11.10767152,11.6246398,12.14359862,12.659277\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,8.649170115,9.141587743,9.645723803,10.15989135,10.68007,11.20131596,11.7186558\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.265533572,7.954841807,8.643880081,9.331430915,10.01437001,10.68857024,11.34967099\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.71873057,13.30012089,13.86249927,14.40218284,14.91608209,15.40214628,15.85939755\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.835332555,10.33838313,10.85310958,11.37733222,11.90675242,12.43631294,12.96103355\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,9.816538949,10.34518401,10.87993677,11.41991818,11.96179373,12.5012272,13.03378424\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,7.289300918,7.965977969,8.645557846,9.325588567,10.0021548,10.6706478,11.32643155\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.81521192,13.38703928,13.94023155,14.47094897,14.97609548,15.45366893,15.90275017\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.48739731,17.05873873,17.56340302,18.01676632,18.42918273,18.80771601,19.15727835\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.92319051,16.58325337,17.17292537,17.70560991,18.19039872,18.63370593,19.04028649\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.36518045,16.88501009,17.35078435,17.77412837,18.16290718,18.52248895,18.85660475\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.53248999,17.07569075,17.57146124,18.02768559,18.44946657,18.84029376,19.20274433\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.4075944,16.13924889,16.80045038,17.39958114,17.94344671,18.43779129,18.88759536\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.54633227,16.21876143,16.82782572,17.38132191,17.88576979,18.34664927,18.76859634\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.46511319,17.01958756,17.52467822,17.98846138,18.41620776,18.81157494,19.17731295\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.14830552,16.75968229,17.29809698,17.77994141,18.21647502,18.61553325,18.98266909\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.17120488,15.92363695,16.59111394,17.18966415,17.73052156,18.22182782,18.66972824\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.9320493,16.57238424,17.13481445,17.63680338,18.0904023,18.50403213,18.88368664\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.54938819,15.37953157,16.12628099,16.7997088,17.40815881,17.95873331,18.45759283\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.5875253,16.25237085,16.85180319,17.39502088,17.88939067,18.34087704,18.75436485\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.79058692,16.26823682,16.69536495,17.08391358,17.44165695,17.77369336,18.08341787\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.73728174,15.46169626,16.10670845,16.68693165,17.21259796,17.69113457,18.12816975\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.40911297,16.96181894,17.45450961,17.90006455,18.30734215,18.68247954,19.0297987\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.08891672,16.71550493,17.27916381,17.79131884,18.2597179,18.68983074,19.08572634\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.33237049,15.17746043,15.93693628,16.62156424,17.24012918,17.80001161,18.30754615\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.88642321,15.62630642,16.29141199,16.89223553,17.43721181,17.93320547,18.3858743\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.13750062,16.76935759,17.33467792,17.84621675,18.31252774,18.73958884,19.13180381\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.93776283,16.57670673,17.13730549,17.63714766,18.08840381,18.49960151,18.87682193\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.08133971,15.84646441,16.52325896,17.12882235,17.67511615,18.17077219,18.62226437\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.76758975,16.43274262,17.015821,17.53517032,18.00350406,18.42974322,18.82026426\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.60324714,15.40401869,16.12588825,16.77796627,17.36789732,17.90226682,18.38684474\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.2548921,15.94693226,16.56858981,17.130317,17.64034232,18.10523954,18.5303362\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.08554135,16.58775666,17.03540161,17.44115275,17.81340678,18.15777011,18.47804459\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.24151187,15.84514457,16.38969305,16.88557377,17.33986167,17.75756157,18.14241177\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.7927446,17.273497,17.7061923,18.10137671,18.46602,18.80476866,19.12077809\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.06050623,16.67379927,17.22658566,17.72976196,18.19064618,18.61437594,19.00477009\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.29622621,16.03655771,16.70581725,17.31232275,17.86288589,18.36329013,18.81856857\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.84200814,15.48680078,16.07321907,16.60792236,17.09661124,17.54415695,17.95473264\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.36649555,16.93975693,17.4608245,17.93834004,18.37806645,18.78404997,19.15933163\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.4155769,16.99513558,17.50695942,17.96637352,18.38380927,18.76646124,19.11938499\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.20938415,15.95614855,16.61952064,17.21503413,17.75358724,18.243096,18.68955458\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.03492242,16.66185389,17.21296488,17.70533549,18.15071222,18.55727258,18.93081488\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.65582893,15.46631855,16.19716717,16.85752808,17.45508818,17.99647448,18.48749815\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.53704136,16.20641682,16.80944929,17.35558023,17.85234152,18.30581415,18.72096788\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.16073859,16.62741602,17.04586666,17.42744445,17.77949688,18.10681306,18.41256317\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.84430088,15.57080399,16.21748526,16.79906026,17.32583377,17.80528575,18.24308361\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,12.3305939,12.83908741,13.296236,13.71276481,14.09600447,14.45098633,14.78121747\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.90451163,16.53481368,17.10211647,17.6177202,18.08930587,18.52231581,18.9208166\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.23492138,15.09146387,15.86068542,16.55363025,17.17932006,17.74533286,18.25816635\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.00323928,15.7187545,16.36428769,16.94914467,17.48091714,17.9658595,18.40917936\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,16.05281046,16.69259657,17.26438282,17.7812518,18.25200459,18.68280524,19.07819821\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.95437827,16.58942403,17.14685758,17.64409676,18.09318056,18.50253746,18.87817482\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.1231797,15.88341087,16.55631262,17.15873068,17.70243744,18.19592625,18.64557063\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.75358479,16.41566152,16.99615103,17.51330934,17.97977491,18.40440862,18.79353956\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,14.62685529,15.42529127,16.1445708,16.79395021,17.38119214,17.91296336,18.39508335\n\"linker [O-]C(=O)C, [O-]C=O, nodes [Mn], topology pcu\",,,15.54413937,16.1992267,16.78985657,17.32525937,17.81275618,18.25822752,18.66646041\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,21.80862459,21.93206285,22.02779799,22.10350706,22.16439072,22.21406976,22.25512618\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,21.94419545,22.02384798,22.08522689,22.13351143,22.17217139,22.20360068,22.22949355\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,21.38796937,21.56992886,21.7130469,21.8275436,21.92051352,21.99699643,22.06064731\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,21.81009251,21.93336318,22.02896955,22.10457761,22.16538061,22.21499425,22.25599691\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,21.93832079,22.01846806,22.08023198,22.12882147,22.16772678,22.1993562,22.22541434\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,21.38409344,21.56637323,21.70975019,21.82445893,21.91760454,21.99423454,22.05800972\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.694725387,4.302148427,4.93002201,5.564351288,6.193895072,6.810270296,7.407702782\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.031590049,4.709174746,5.396297882,6.078084003,6.743508606,7.385076845,7.99825284\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.17771698,3.775705603,4.406588968,5.053755677,5.703154016,6.343882499,6.968129587\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.510288166,4.11067994,4.735380553,5.36965399,6.001567203,6.62214227,7.225117839\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.145223245,4.816462235,5.497071934,6.172382276,6.831512585,7.467066142,8.074570292\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.459613484,4.076105453,4.716755786,5.366240689,6.012119201,6.645054235,7.258581879\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.25577688,3.863224329,4.498475325,5.14582808,5.792296079,6.427967637,7.045847349\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.004929325,4.681412438,5.367561032,6.048643601,6.713678662,7.35516666,7.968545802\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.434327886,4.052701708,4.692314435,5.338704874,5.980293593,6.60846567,7.217295865\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.554582014,4.167905153,4.802298575,5.4435142,6.080117486,6.703593809,7.308089046\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.639061491,4.343315049,5.058630514,5.768420411,6.460577159,7.126996086,7.762857193\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.034671796,3.631276981,4.263886609,4.914992069,5.569840345,6.217022522,6.848379955\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.639946646,4.253726882,4.888156103,5.528862007,6.164373762,6.786186413,7.388477828\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.87835514,4.559574341,5.252225738,5.94075751,6.613601892,7.262859244,7.883709025\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.236022044,3.83130551,4.455764397,5.094133905,5.733592209,6.364216783,6.978898397\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.236621759,3.867671578,4.523438366,5.187958503,5.848311137,6.494838569,7.120890257\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.026013618,4.703714058,5.39087105,6.072715494,6.738273426,7.380074089,7.993593545\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.429548736,4.027329768,4.651895416,5.288080017,5.923402099,6.548365127,7.156279784\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.693665813,4.301048815,4.928917062,5.563264317,6.192840445,6.809255651,7.406730874\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.033036911,4.710673535,5.397805665,6.07956853,6.744947537,7.386455933,7.999563966\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.175742655,3.773632007,4.404459835,5.051607351,5.701015621,6.341776601,6.966073086\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.511097687,4.111689425,4.736546559,5.370937216,6.00293359,6.623563133,7.226569536\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.129797249,4.800707558,5.481204598,6.156579719,6.815917022,7.451788682,8.059695241\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.450008025,4.065548026,4.705363895,5.35416304,5.999518392,6.632092038,7.245408888\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.262285109,3.870050321,4.505493731,5.152926912,5.799381757,6.434965847,7.052701615\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.003512821,4.680107387,5.366376733,6.047581083,6.712733689,7.354332112,7.967813357\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.432977025,4.051289632,4.690872722,5.337256481,5.978855118,6.607049036,7.215909551\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.55543398,4.168824656,4.803258873,5.444493364,6.081098167,6.704562648,7.309036011\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.635064772,4.339242562,5.054581385,5.764469009,6.45677816,7.123390146,7.759475761\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.033452358,3.630040922,4.262647634,4.913762419,5.568630258,6.215840151,6.847231514\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.641757575,4.25551583,4.88989479,5.530531844,6.165963664,6.78769078,7.389894889\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.880093409,4.561440964,5.254172297,5.94274465,6.615598473,7.264841191,7.88565816\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.237912951,3.833063749,4.457374851,5.095592774,5.73490374,6.365390269,6.979945835\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.236494179,3.867151475,4.522542758,5.186711768,5.846733794,6.492938996,7.118660153\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,4.024878622,4.702139937,5.388926736,6.070471445,6.735795593,7.37742039,7.990812296\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,3.429469535,4.027268496,4.65187442,5.288109526,5.923484322,6.548497381,7.156456715\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.467494058,10.20696512,10.93249532,11.63862817,12.32081126,12.97553273,13.60032764\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.298448203,9.066279769,9.824324669,10.5691692,11.29662807,12.00247927,12.68299015\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.21748708,10.95053702,11.65887094,12.34005957,12.99216316,13.61378182,14.20407339\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.618094275,10.35634855,11.0757316,11.77278592,12.44435077,13.08784013,13.70138159\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.608475143,10.34607808,11.0694612,11.77318321,12.45272969,13.10463874,13.72649997\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.308478746,9.076510914,9.836239079,10.58362155,11.31399633,12.02281219,12.70612879\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.23349339,10.9612982,11.66698152,12.34721226,12.99944188,13.62185864,14.21334311\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.73041991,10.47092541,11.19364429,11.89399067,12.56823168,13.21355502,13.82805997\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.569585525,10.31773378,11.04646465,11.75209464,12.43137282,13.08170415,13.70125245\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.07720874,10.81907253,11.53658534,12.22727527,12.8889498,13.51992809,14.11913611\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.070267069,8.838773954,9.596159268,10.33975245,11.06596676,11.7709968,12.45135683\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.442009171,10.20114708,10.94085466,11.65726238,12.34685554,13.00681967,13.6351778\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.38177038,10.13710208,10.87531803,11.59173039,12.28229896,12.94386967,13.5742428\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,7.925762405,8.709797686,9.481271291,10.23739843,10.97463905,11.68930922,12.3780724\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.07266089,10.83252742,11.56227138,12.26115462,12.9281955,13.56254736,14.16371008\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.736871758,10.47031838,11.1872935,11.88358439,12.55536673,13.199534,13.81384094\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.545860708,10.28639962,11.00968897,11.71133485,12.3877092,13.03602387,13.65433637\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.264685632,9.032163704,9.788603214,10.53110169,11.25593278,11.95922524,12.63748175\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.23208112,10.97906232,11.69724156,12.38529133,13.04208926,13.66683139,14.25910765\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.737485076,10.4854442,11.21088477,11.91093441,12.58307204,13.22531627,13.83631931\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.445323952,10.22846007,10.98304236,11.70708581,12.39896781,13.05751675,13.68206896\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.14208018,10.88412512,11.59882498,12.28448616,12.93974974,13.56365304,14.1556704\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.263386407,9.023805353,9.775136755,10.51410208,11.23660283,11.93844773,12.61588414\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.517762345,10.26082858,10.98684839,11.69165646,12.37153349,13.02349052,13.64538159\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.467627082,10.20690582,10.93225602,11.63822203,12.320252,12.97483413,13.59950318\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.298625378,9.066435323,9.824449419,10.56925851,11.29668011,12.00249386,12.68296802\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.21752208,10.95053677,11.65881946,12.33994418,12.99197594,13.61351945,14.20373631\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.619261669,10.35741804,11.07669031,11.77362373,12.44506153,13.0884217,13.70183527\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.605145107,10.34318954,11.0669674,11.77103877,12.45089191,13.10306834,13.72516144\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.311348179,9.079305253,9.838871055,10.58604006,11.31617733,12.02475042,12.70783119\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.23538281,10.9629515,11.66836968,12.34833336,13.00031029,13.62249748,14.21377934\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.732357393,10.4723568,11.19454689,11.89438493,12.56816475,13.21308764,13.82725712\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.571953881,10.31964739,11.0479979,11.75330874,12.43231862,13.08242433,13.70178307\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.07697232,10.81898864,11.5366016,12.22735506,12.88906793,13.52006755,14.11928569\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.069730088,8.838244897,9.595606206,10.33915576,11.06531649,11.77029,12.45059523\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.442543173,10.20143913,10.94093168,11.65714771,12.34657049,13.00638406,13.63461002\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.379995249,10.13536636,10.87361278,11.59004933,12.28063799,12.94222624,13.57261542\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,7.924399921,8.708621651,9.480264795,10.2365424,10.97391381,11.68869561,12.37755241\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.07230756,10.83245225,11.56245145,12.26156363,12.92880478,13.56332749,14.16463244\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.736067829,10.46972406,11.18685442,11.88325992,12.55512574,13.19935223,13.81369934\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.546206293,10.28689181,11.01032864,11.71211344,12.3886125,13.03703497,13.65543768\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.263074907,9.031019071,9.78794096,10.53091082,11.25618195,11.95987015,12.63847151\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.2310306,10.9782455,11.69661718,12.38482429,13.04175069,13.66659796,14.25896059\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.740055808,10.48789694,11.21321927,11.91315486,12.58518608,13.22733386,13.83825165\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.445812112,10.22858811,10.98287136,11.70666599,12.3983419,13.0567214,13.68113522\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.14347254,10.88509766,11.5994263,12.28476152,12.93974197,13.56340249,14.15521454\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,8.262070246,9.022702963,9.774261625,10.51345213,11.23616496,11.938202,12.61580708\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,9.519847579,10.26268991,10.98852836,11.69318375,12.37292787,13.0247662,13.64654928\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.25961643,12.05008561,12.821289,13.56552483,14.27642044,14.94951629,15.58224901\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.03128642,11.86736336,12.66491205,13.42126872,14.13477096,14.80474889,15.43141719\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.3363391,12.1184011,12.88476718,13.62649209,14.33633226,15.00923817,15.64225905\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.58902331,12.38988821,13.15584752,13.88343486,14.57050731,15.21609807,15.82022426\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.71092629,12.47414224,13.21975909,13.93957292,14.62712581,15.27803308,15.88983571\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.29173233,12.13387849,12.93556897,13.6940532,14.40771765,15.07604609,15.699473\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.54432216,12.3572618,13.13350904,13.86959868,14.563444,15.2141949,15.82202829\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.86528413,12.64551284,13.40322805,14.13064438,14.82194074,15.47343264,16.08333293\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.09160325,11.91971081,12.70864738,13.45634017,14.16160671,14.82410654,15.44424241\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.05957823,11.84897759,12.6213492,13.36888016,14.08488796,14.76452639,15.40484523\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.92404109,11.70389024,12.47015844,13.2144863,13.92962145,14.61018549,15.2527652\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.38077042,12.20084774,12.98057468,13.71828266,14.41308433,15.06486028,15.67418299\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.25729661,12.04713991,12.81785584,13.56172479,14.2723549,14.94526806,15.57788409\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.03149492,11.86713897,12.6642855,13.42027977,14.13346289,14.80316465,15.4295971\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.33939066,12.12117494,12.88718318,13.62850829,14.33793901,15.01044936,15.64310367\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.59324991,12.3941153,13.16006766,13.88762466,14.57463826,15.22014265,15.82415889\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.71498911,12.47763652,13.2227636,13.94215158,14.62933219,15.27991301,15.89142882\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.29414171,12.13595809,12.93737305,13.69561912,14.409072,15.07720877,15.70045976\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.54261794,12.3552006,13.13114894,13.86699966,14.56066214,15.21127958,15.81902127\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.8560435,12.63684876,13.39503232,14.1228475,14.81449741,15.4663121,16.07651279\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.09230966,11.92057901,12.7095982,13.45732662,14.16260302,14.82510048,15.44523001\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.04553204,11.83595604,12.60921383,13.35754417,14.07429484,14.75463604,15.39562556\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,10.9331941,11.71171302,12.47682199,13.22015075,13.93443397,14.61427849,15.25625542\n\"linker n1ccc(cn1)c1ccnnc1, nodes [Ag][Ag][Ag], topology pts,sur\",,,11.38413772,12.20322987,12.9821237,13.7191398,14.41337653,15.06469847,15.67366203\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,21.15293274,21.41836047,21.62616705,21.79175573,21.92575409,22.03566908,22.1269165\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,20.94779917,21.24568495,21.47900434,21.66496054,21.81544872,21.93888405,22.04134407\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.641600465,4.255337097,4.89246139,5.537791445,6.178992463,6.806834907,7.41497061\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.726014294,4.390478987,5.068220609,5.743966744,6.406401406,7.047723682,7.663050833\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.388569067,4.01360061,4.663180076,5.321381638,5.975347719,6.615506705,7.235301867\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.098291795,3.538283545,4.01858823,4.529811059,5.062039297,5.605992975,6.153694733\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.309824597,3.755593093,4.240676009,4.755534823,5.290014492,5.834648721,6.381377632\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.240143551,3.706447957,4.210779304,4.742543978,5.291259646,5.847544133,6.403624199\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.206048972,3.69699712,4.223712114,4.775564926,5.341983541,5.913586393,6.482717839\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.198028955,3.688212864,4.214216283,4.765342963,5.330987117,5.901742302,6.469927008\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.252891947,3.85114395,4.477315207,5.116165559,5.755028707,6.38417054,6.996658235\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.386414799,4.035529744,4.70962243,5.390806988,6.065123224,6.722521357,7.356381725\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.657350567,4.156839967,4.688147119,5.240666367,5.804137442,6.369647351,6.930071811\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.440525178,4.089792146,4.763270327,5.443169853,6.115630764,6.770695113,7.401821398\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.200805911,3.801766305,4.4322709,5.07639682,5.720931872,6.355745229,6.973639642\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.129441101,3.735320288,4.369647116,5.016701691,5.663483232,6.300041281,6.919315848\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.103287406,3.730796594,4.390691047,5.064334288,5.736711112,6.396678148,7.036615621\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.243587834,3.894676538,4.573448318,5.261154566,5.943056128,6.608487655,7.250384154\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.318944443,3.936208373,4.577110988,5.226582764,5.87247185,6.505680722,7.119908473\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.633752247,4.247551764,4.884832402,5.530393172,6.171878119,6.800038686,7.408511255\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.736941483,4.402266693,5.080605172,5.75671884,6.419327526,7.060664655,7.675878709\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.38922103,4.01456895,4.664385487,5.322763028,5.97685734,6.617107146,7.236964035\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.097650617,3.537735898,4.018103852,4.529370654,5.061630946,5.60560961,6.153332398\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.310379925,3.755964068,4.240912827,4.755673274,5.290079516,5.834657331,6.381341163\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.239566295,3.705941121,4.210340581,4.742171038,5.290950233,5.84729648,6.403437371\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.205523524,3.696731803,4.223645147,4.775649654,5.342184208,5.913875332,6.483073541\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.198312039,3.688646973,4.214780832,4.766014956,5.331742913,5.902559007,6.470783372\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.250626808,3.848680566,4.47475079,5.113571461,5.7524554,6.381652456,6.994217854\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.384205391,4.033106243,4.707046007,5.388131843,6.062395129,6.719777659,7.353652071\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.656702587,4.155891993,4.686930435,5.239217809,5.802496248,6.367852194,6.928158628\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.44097881,4.089770331,4.76289633,5.442541254,6.114823041,6.769765689,7.400813408\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.189859012,3.790476937,4.420906959,5.065166373,5.709985826,6.345185771,6.963530266\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.13302851,3.739611578,4.374505395,5.021991785,5.669080772,6.305837446,6.925218948\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.108124218,3.736496356,4.397079184,5.071238085,5.743971987,6.404157884,7.044198378\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.240416281,3.891119984,4.569584338,5.257067364,5.938825058,6.604181524,7.246059267\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,3.312972798,3.929882436,4.570529503,5.219850434,5.865685129,6.498921742,7.113243591\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,8.168412964,8.914702095,9.66008063,10.39983476,11.1279073,11.83823038,12.52551512\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.238521895,9.985418772,10.724297,11.44716569,12.14750507,12.82037947,13.46237059\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.999679454,10.70151136,11.39606513,12.07624227,12.73595049,13.37044965,13.97639448\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.332727867,10.09006115,10.82917307,11.54567874,12.23575771,12.89640206,13.52550782\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,6.823771953,7.632866548,8.439283329,9.235189148,10.01404733,10.77044405,11.50006374\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.343186375,10.07653401,10.79834676,11.50245542,12.18371031,12.83814416,13.46297035\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.683818126,10.41974691,11.13588039,11.82872052,12.49512308,13.13261795,13.73951651\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,7.751173578,8.497562121,9.240699506,9.975877125,10.69802764,11.40224971,12.08423332\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.804875022,10.51715259,11.21300211,11.88859281,12.54041521,13.16564664,13.76227676\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.173197396,9.911554607,10.63585486,11.34104074,12.02278466,12.67767107,13.30324596\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.338829069,10.05051694,10.75258436,11.43930323,12.10570853,12.74782712,13.36273845\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.748401588,10.45364363,11.14595164,11.82030037,12.47238092,13.09883773,13.69730401\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,7.796376697,8.529149303,9.259360705,9.982887694,10.69487796,11.39044628,12.06519826\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.769801234,10.48167714,11.17866447,11.85615749,12.51020412,13.13773335,13.73659972\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.248987596,9.962607826,10.66698582,11.35629076,12.02548191,12.67052498,13.28844779\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.91097335,10.68744847,11.44608838,12.17886279,12.87962279,13.54425918,14.17051162\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.63665712,11.29376892,11.94912302,12.59519479,13.22449634,13.8308641,14.409866\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.867639091,10.63736869,11.39292474,12.12502253,12.82667278,13.49319524,14.12193698\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,8.151257629,8.899212962,9.645994724,10.38694712,11.1160553,11.82728312,12.5153658\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.228614493,9.97650766,10.71613669,11.43958189,12.14037475,12.81361672,13.45591614\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.992677508,10.69601107,11.39184402,12.0731177,12.73376446,13.3690623,13.97568139\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.330089945,10.08781198,10.827149,11.54379284,12.23396697,12.89468756,13.52386303\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,6.816416426,7.626776938,8.434156465,9.23078865,10.01019165,10.76699618,11.49692208\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.328537303,10.06342971,10.78644281,11.49151118,12.17355572,12.82865725,13.45406199\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.678156257,10.41443192,11.1308385,11.82390934,12.49051861,13.12820639,13.73528931\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,7.754445609,8.500936258,9.244048287,9.979122513,10.70112459,11.40517489,12.0869775\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.802539701,10.51519321,11.21132714,11.88714117,12.53914542,13.16452964,13.76129129\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.171039113,9.910299901,10.63531721,11.34107588,12.02327721,12.67852682,13.30438722\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.339391404,10.05087126,10.75278795,11.43940413,12.10574517,12.74782877,13.36272627\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.767180568,10.47068692,11.16150895,11.83456894,12.48551999,13.11097819,13.70855514\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,7.799603745,8.531881184,9.26167247,9.984835672,10.69650849,11.39179973,12.06631072\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.770351611,10.48230613,11.17937554,11.85694794,12.51106691,13.13865876,13.73757674\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.259790729,9.972591117,10.67617459,11.36471849,12.03319062,12.67756288,13.29486638\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.90873529,10.686135,11.44548691,12.17880666,12.8799807,13.54492764,14.17140916\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.63377829,11.29139877,11.94715839,12.59355779,13.22312636,13.82971306,14.40889537\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,9.871415842,10.64060773,11.3957291,12.12746951,12.82882205,13.49509383,14.12362259\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,12.071492,12.82053366,13.5363133,14.21662019,14.85999574,15.46571438,16.03374264\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.79441716,11.64698768,12.45853802,13.22773378,13.9533639,14.63479375,15.27212444\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.80046016,11.56738001,12.30884531,13.02162952,13.70273512,14.34986522,14.96159116\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.50942836,11.27696566,12.01934556,12.73375401,13.4174306,14.06816606,14.68450853\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,11.98828329,12.74390341,13.4655757,14.15120381,14.79940627,15.40951491,15.98154241\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.7989862,11.65383372,12.46685727,13.23694359,13.96304572,14.64465083,15.28194989\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.76128808,11.53148603,12.27575239,12.99098147,13.67425708,14.32333729,14.93683129\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,10.50852815,11.27507754,12.01673131,12.73061992,13.4139384,14.06444153,14.68064863\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,15.02209518,15.82819311,16.54584362,17.18685601,17.76112726,18.27699647,18.74153822\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,15.32951781,16.05296198,16.70728793,17.29960273,17.8363655,18.3233478,18.76567754\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,14.99685405,15.80740326,16.52843207,17.17205517,17.74837964,18.26589056,18.73176527\n\"linker [O-]C(=O)c1cnccn1, nodes [Zn], topology pcu\",,,15.2866172,16.01336743,16.67067478,17.26567679,17.80486534,18.29404306,18.73836556\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,19.22908768,19.71781492,20.10804879,20.42381954,20.6824554,20.89664371,21.07581063\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,19.22934515,19.7180311,20.10823266,20.4239777,20.6825928,20.89676413,21.075917\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,11.10416504,12.0612998,12.95106091,13.77385499,14.53135242,15.2262605,15.86204211\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,11.10746907,12.06597975,12.95651308,13.77967741,14.53728274,15.23213154,15.86775082\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,11.10439971,12.06147909,12.95119892,13.77396215,14.53143638,15.22632689,15.86209508\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,11.10747432,12.06598739,12.95652219,13.77968742,14.53729326,15.23214229,15.86776163\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,8.596614012,9.197131951,9.761362477,10.28990817,10.78261115,11.23958605,11.66154689\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.765288931,4.45375408,5.128188417,5.781907047,6.410782546,7.01231805,7.585155619\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.37756226,4.042799708,4.724702709,5.407801145,6.080156565,6.733244447,7.361514564\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,8.572362404,9.175712517,9.74222317,10.27263913,10.76690817,11.22522017,11.64834188\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.753004292,4.443654255,5.119849926,5.774986651,6.405007251,7.007473413,7.581074696\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.380153713,4.045443531,4.727354474,5.410433895,6.082752541,6.735791079,7.364002571\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,8.597301583,9.197710393,9.761851293,10.2903236,10.78296642,11.23989184,11.66181177\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.765299521,4.453774644,5.128216406,5.781940206,6.410818773,7.012355209,7.585191363\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.377448482,4.042662548,4.724548026,5.407634225,6.07998189,6.733065657,7.361334524\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,8.57258302,9.175895793,9.742375665,10.27276636,10.7670147,11.22530974,11.64841754\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.753248082,4.443925961,5.12013911,5.775284402,6.405304986,7.007761652,7.581341956\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,3.380576656,4.045916284,4.727862897,5.410965378,6.083296477,6.736338908,7.364547609\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.561113757,8.370591381,9.154729336,9.914536061,10.64972341,11.35911776,12.0411812\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.721908981,8.595135668,9.44766023,10.27429091,11.07053439,11.83281083,12.5585618\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,9.252737889,10.06275041,10.84017477,11.58273161,12.28897177,12.95815464,13.59015483\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.563439618,8.373414207,9.157783894,9.917664668,10.65283197,11.36215057,12.04410622\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.729287284,8.602262167,9.454447061,10.2807102,11.07658739,11.83851209,12.56393125\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,9.255375321,10.06560054,10.8430601,11.58555449,12.29168095,12.96072578,13.59257911\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.561027191,8.370519222,9.154670031,9.914488078,10.64968528,11.35908812,12.04115882\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.721884165,8.59511145,9.447636375,10.27426728,11.07051093,11.83278756,12.55853878\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,9.252948894,10.06292039,10.84031005,11.5828378,12.28905372,12.95821648,13.59020004\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.563581762,8.373542979,9.157898576,9.917765436,10.65291953,11.36222592,12.04417048\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,7.729309906,8.602284868,9.454473452,10.2807425,11.07662667,11.83855863,12.56398472\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,9.255326534,10.06558545,10.84307786,11.58560286,12.29175683,12.96082562,13.59269925\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,15.8781821,16.64286911,17.3234737,17.92881238,18.46689904,18.94515722,19.37043226\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.78104901,14.74461144,15.60205122,16.36659733,17.04935933,17.65987442,18.20646686\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.90232949,14.76028203,15.53066551,16.22577688,16.85487688,17.42527047,17.94301263\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,15.0327021,15.8269798,16.52301926,17.13730272,17.682693,18.16935085,18.60543091\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,15.60495716,16.40548752,17.11565245,17.74558124,18.30429846,18.80000603,19.24015204\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.85956396,14.81464417,15.6642403,16.42176115,17.09834101,17.70346719,18.24538322\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.93141616,14.78598858,15.55349626,16.24615446,16.87315269,17.4417364,17.95791177\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,14.75801682,15.58705962,16.31210914,16.95071756,17.51662809,18.02070985,18.47168248\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,15.88278532,16.64685316,17.32695073,17.93187004,18.46960649,18.94756962,19.37259404\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.78258467,14.74598084,15.60327779,16.36770066,17.05035582,17.66077788,18.2072889\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.90132175,14.75938475,15.52986647,16.22506397,16.85423903,17.42469786,17.94249674\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,15.03126172,15.82568627,16.52185352,17.13624831,17.68173581,18.16847883,18.60463373\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,15.60462597,16.40519779,17.1153969,17.74535426,18.3040956,18.79982374,19.23998743\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.85864666,14.81382473,15.66350764,16.42110474,17.0977513,17.70293574,18.24490269\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,13.9322046,14.78668017,15.55410648,16.2466961,16.87363622,17.44217037,17.9583032\n\"linker Oc1cc(c(cc1P(=O)(O)[O])O)P(=O)(O)[O], nodes [Zn], topology \",,,14.75679526,15.58603065,16.31123554,16.94997005,17.51598345,18.02014953,18.47119149\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,20.13439113,20.52314194,20.83846015,21.09722328,21.31181193,21.49146551,21.64318059\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,20.27585062,20.64692728,20.9475952,21.19415491,21.39851712,21.56954575,21.71393926\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,18.8005976,19.16863661,19.4674283,19.71281429,19.91643827,20.0870039,20.23111103\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,19.94155841,20.31708658,20.6222312,20.87307598,21.08142592,21.25610404,21.40380431\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.333661524,3.982091309,4.655416571,5.336199114,6.010593896,6.668487653,7.303121213\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.33333156,3.99094166,4.672448665,5.360102263,6.039969047,6.701984807,7.33951252\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.354153029,4.003741577,4.677838707,5.359056017,6.033603971,6.691424083,7.325807344\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.358737124,4.015137695,4.695371274,5.381796685,6.060538869,6.721557943,7.358220479\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.423425957,4.079279827,4.757544013,5.441112419,6.116511446,6.773980224,7.407067482\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.369502972,4.019676721,4.694195681,5.375690144,6.050376549,6.708192415,7.34241983\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.435652101,4.089684112,4.766190557,5.448144728,6.12211953,6.778375538,7.410465393\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.348389903,3.998619936,4.673550066,5.355722617,6.03127971,6.690104543,7.325443347\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.345220053,3.995118818,4.669586668,5.351213686,6.02618294,6.684408739,7.31915903\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.418371383,4.073883421,4.751731502,5.434850327,6.109800225,6.766846188,7.399555149\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.335283134,3.986103887,4.661370548,5.343638004,6.019071343,6.677577343,7.312422737\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.412125906,4.067924412,4.74596844,5.429213399,6.10423342,6.761301497,7.393988816\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.343625346,4.002080083,4.684320873,5.372603141,6.052998805,6.715450053,7.353327557\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.346777058,3.996223137,4.670239243,5.351430914,6.02600401,6.683895081,7.318389465\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.36526169,4.021415985,4.701302594,5.387318067,6.065620456,6.726195602,7.362428345\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,3.354464015,4.003305425,4.676890717,5.357801772,6.032211886,6.690025338,7.3244996\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.453756716,10.22340705,10.96775832,11.68352079,12.36825101,13.0202842,13.63867733\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.458184225,10.23348188,10.9816569,11.6997804,12.38572716,13.03810085,13.65617773\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.535178712,10.30585537,11.05099641,11.76740632,12.4526713,13.10512779,13.72382564\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.577538016,10.35256143,11.10085596,11.81945176,12.50613592,13.1594141,13.77847401\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.571733031,10.34096498,11.08415115,11.7983334,12.48126688,13.13140044,13.74785336\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.590849293,10.35697801,11.09748799,11.80947843,12.49069054,13.13952284,13.75503022\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.548977517,10.31720405,11.05945445,11.77277613,12.45493285,13.10438032,13.72024126\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.542754365,10.31019325,11.05124222,11.76326098,12.4441872,13.09256343,13.7075467\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.497457102,10.26416758,11.00516105,11.71754122,12.39905509,13.04810932,13.66376888\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.479171624,10.24913422,10.99311232,11.70810446,12.39183181,13.04271975,13.65987337\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.371207819,10.13689838,10.87651355,11.58732474,12.26720856,12.91466289,13.52881149\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.379558555,10.14791911,10.89030632,11.60375795,12.2860379,12.9356046,13.5515831\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.516171019,10.29370512,11.04371829,11.7634046,12.45071637,13.10430571,13.72347936\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.493713381,10.26473289,11.00999463,11.7263265,12.41136857,13.06351829,13.68188034\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.591000174,10.36474431,11.11203117,11.82979508,12.51576935,13.16843027,13.78694924\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,9.571074376,10.34194447,11.08729044,11.80392803,12.48945011,13.14219496,13.76121046\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.788092972,7.603646943,8.414713372,9.21412002,9.995737234,10.75440094,11.4859463\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,8.037441769,8.768658749,9.497021645,10.2186931,10.92869731,11.62194226,12.29387099\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,7.984571249,8.716470395,9.445390199,10.16755638,10.87803701,11.57176687,12.2442027\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.786878782,7.606307983,8.419967223,9.221097828,10.0038777,10.76336572,11.49555265\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.79950931,7.608138495,8.413855915,9.209218936,9.98789461,10.7445523,11.47488204\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,8.07311503,8.800999258,9.526504038,10.245797,10.95387455,11.64559863,12.31635844\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,8.119161981,8.849558025,9.577256395,10.29841751,11.00803536,11.70098058,12.37266202\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.891261012,7.704050763,8.513295448,9.311651416,10.09279524,10.85138483,11.58310884\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.670953684,7.488460517,8.303014527,9.106551732,9.892263965,10.65452163,11.38888077\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,8.036581071,8.775504857,9.511752554,10.24107856,10.95817665,11.65773088,12.3350626\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,8.068856468,8.80900547,9.546227785,10.27630419,10.99394853,11.69386427,12.37139329\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.922184993,7.751070529,8.573895083,9.383311038,10.1730972,10.93809859,11.6742458\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.901256468,7.723288776,8.541127022,9.34675884,10.13350594,10.89591101,11.62971341\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,8.032214001,8.769230233,9.503371448,10.23042973,10.94514981,11.6422705,12.31716468\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,8.036136753,8.771437294,9.503873542,10.22936275,10.94273235,11.63876595,12.31285121\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,6.954372733,7.772337097,8.58675158,9.389723419,10.1746024,10.9358931,11.66925623\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.86759817,14.78393424,15.59535493,16.31774713,16.96385804,17.54398946,18.06657293\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.93227017,14.81144608,15.59654568,16.2998216,16.93173322,17.50113755,18.01553524\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,14.69561328,15.48949729,16.19620788,16.82883939,17.39773214,17.91116965,18.37590959\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.60624393,14.51295676,15.32450296,16.05249209,16.70709073,17.29708084,17.83001663\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,12.72283211,13.4871189,14.17767399,14.80257492,15.36896228,15.88307024,16.35034243\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.90159914,14.78561907,15.57222495,16.27542097,16.90663482,17.47522634,17.98893406\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,14.87254977,15.57662338,16.20881891,16.77943907,17.29644469,17.76615874,18.19375899\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,14.46219433,15.28866353,16.0251741,16.68471086,17.27777104,17.81290288,18.29715338\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.74485124,14.61033812,15.38200297,16.0730015,16.69410467,17.2541753,17.76058149\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,14.09970521,14.95100069,15.71126051,16.39313155,17.006888,17.56096032,18.06236672\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.66882839,14.56585897,15.36358746,16.0761519,16.71521584,17.29039057,17.80964436\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,14.46822877,15.26741615,15.98733873,16.6373997,17.22563268,17.75890032,18.2431067\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.75684283,14.55445945,15.27309083,15.92153718,16.50772453,17.03862128,17.52029956\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.71464487,14.64231452,15.46332596,16.19380079,16.8467339,17.43265388,17.9601857\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,13.61663868,14.50614525,15.30418794,16.02135617,16.66711568,17.2497627,17.77650953\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,14.47953668,15.32449399,16.07480183,16.74464308,17.34533373,17.88600059,18.37411761\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,16.57144328,17.48649927,18.26628211,18.93148799,19.50040847,19.9886966,20.40949769\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,15.68030831,16.72355269,17.61459556,18.37579354,19.02739645,19.58696791,20.06937499\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,15.95757628,16.96948711,17.83208372,18.56813316,19.19779064,19.73831965,20.20422694\n\"linker [O-]C(=O)c1ccc(cc1)C(=O)[O-], nodes [Ga], [O], topology rna,pcu\",,,12.82313839,13.72777852,14.50893331,15.18187317,15.76172363,16.26229974,16.69569291\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.15915619,21.61989202,21.98590431,22.28095424,22.52193697,22.72108704,22.8874152\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.19870873,21.65604262,22.01855782,22.3102572,22.54815696,22.74453702,22.90841086\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.20803614,21.66089796,22.02075822,22.310921,22.54796262,22.74389145,22.90755492\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.52882414,21.93561149,22.25801258,22.51742683,22.72900778,22.90368209,23.04946508\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.19242458,21.64774934,22.00953245,22.30122324,22.53949918,22.73643979,22.90094341\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.4230962,21.84689722,22.18258886,22.45256381,22.67266382,22.85430287,23.00584831\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.32621786,21.76148788,22.10726441,22.38600742,22.61368151,22.80184469,22.95900809\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.36851305,21.80138143,22.14409371,22.41960625,22.64414561,22.82939484,22.98391347\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.55087344,21.97422187,22.30521666,22.56851878,22.78119482,22.95531608,23.09959368\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,21.71493476,22.11292609,22.42381109,22.67095293,22.87047982,23.03377793,23.16905218\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.66254813,4.344772845,5.045675951,5.747084707,6.435385371,7.101158123,7.738499427\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.276033333,3.94300464,4.639867689,5.345831622,6.044814456,6.725353992,7.379980688\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.77917592,4.465911692,5.16929501,5.87122218,6.558354481,7.221617299,7.855447617\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.405528388,4.077387449,4.777021086,5.48375249,6.181803751,6.860070353,7.51142444\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.492205682,4.177012881,4.88006141,5.584040973,6.275617708,6.945393801,7.587399835\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.282071572,3.969854455,4.678839433,5.390663441,6.091152649,6.770272032,7.421588673\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.646505979,4.330215522,5.032701631,5.735683033,6.425473171,7.092610684,7.731173582\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.276163419,3.943949987,4.641482161,5.347975598,6.047360376,6.728189036,7.383007407\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.767756945,4.454322886,5.157619438,5.859558821,6.546801293,7.210261209,7.844359871\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.404101948,4.076056136,4.775616243,5.482176759,6.179997756,6.857987693,7.509015734\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.48976338,4.175363686,4.879393792,5.584397884,6.276948773,6.947596372,7.590347829\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.291646832,3.980875951,4.691143958,5.404031217,6.10534205,6.785045348,7.436728131\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.649040585,4.333241546,5.036295286,5.739845107,6.430155687,7.097739072,7.736662686\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.277350048,3.944164446,4.640691851,5.346230678,6.044762382,6.724865545,7.379093953\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.778819868,4.465600581,5.169026746,5.870995176,6.558166658,7.221465783,7.855328803\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.407115739,4.078908536,4.778408253,5.484952757,6.182768311,6.860745997,7.511748207\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.495456916,4.179986487,4.882811527,5.586603818,6.27801777,6.947648102,7.589520728\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.282329879,3.971214903,4.681134513,5.393722946,6.094816082,6.774395475,7.426047657\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.638699214,4.322900426,5.0261076,5.729918615,6.420561816,7.088521144,7.727842954\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.272308261,3.939603556,4.636822249,5.343150731,6.042489789,6.72336569,7.378302122\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.775474302,4.461493245,5.164254684,5.865673384,6.552415382,7.21540071,7.849054889\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.402967346,4.073364772,4.771583718,5.477037877,6.173999102,6.851381236,7.502053523\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.496057791,4.182106263,4.88640419,5.591517662,6.28404861,6.954576901,7.597136875\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,3.291752168,3.981802866,4.692872474,5.406477644,6.108392833,6.788579597,7.440630826\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.175930253,9.823249253,10.48061833,11.14001348,11.7933881,12.43362226,13.05495093\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.221124727,9.870246968,10.52808637,11.18723566,11.83995946,12.47929562,13.09956387\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.304007796,9.935918078,10.58110974,11.23075288,11.87620414,12.50990356,13.1257609\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.355713336,9.984319322,10.62671494,11.2739404,11.91721934,12.54888849,13.1627917\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.026105365,7.818819278,8.603917487,9.375920738,10.13015316,10.86262213,11.57002544\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.885299621,8.722469228,9.542350639,10.34116305,11.11497986,11.86020689,12.57391104\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.291731168,10.11296199,10.90494398,11.66404817,12.38771679,13.07437847,13.72333222\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,8.110899178,8.924825262,9.722210924,10.4993333,11.2525073,11.9784,12.67427988\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.201760739,10.02210656,10.81203679,11.5685266,12.28950245,12.97373778,13.62074692\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.89144421,8.717317523,9.526280496,10.3149231,11.07958764,11.81683776,12.52379891\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.034958524,7.935946633,8.827938697,9.700553825,10.54572692,11.35750883,12.13182402\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.074574521,7.854722012,8.623019458,9.375396339,10.10873716,10.82040177,11.50809949\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,6.895148296,7.683880104,8.4637142,9.229959824,9.978670673,10.70639028,11.41013754\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.143984461,9.795278547,10.45602681,11.11833411,11.77423482,12.41666679,13.03991045\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.194981463,9.845723375,10.50516919,11.16589518,11.8201457,12.46094106,13.08258832\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.298790108,9.932280997,10.57846507,11.22867357,11.87439656,12.50817654,13.12399794\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.320544907,9.952386307,10.5975255,11.2471271,11.89249704,12.52602649,13.14159594\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.091924224,7.866524508,8.637571176,9.398699634,10.14455272,10.87060344,11.57312661\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.865029322,8.701352308,9.52104896,10.32010044,11.09441918,11.84030461,12.55475411\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.300973666,10.12021969,10.91051827,11.66818609,12.39062839,13.07624671,13.72431818\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,8.108819424,8.922870006,9.720208215,10.49723497,11.25031809,11.97614379,12.67198456\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.201152453,10.02246357,10.81315701,11.5702638,12.2917382,12.97637056,13.62368827\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.888656157,8.715425907,9.524782769,10.31350274,11.07806057,11.81510959,12.52183335\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.025970168,7.925030261,8.815478938,9.686921088,10.5312526,11.34247721,12.11647219\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.082805579,7.860606539,8.626524414,9.376768669,10.10834207,10.81862778,11.50530799\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,6.882019107,7.675420967,8.458932922,9.228033684,9.978929578,10.70829576,11.41326163\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.162598191,9.811502608,10.47031218,11.13104673,11.78566951,12.42705814,13.04944281\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.201621441,9.852737447,10.51232405,11.1730518,11.82721886,12.46787705,13.08935263\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.304722968,9.93722419,10.58288881,11.23290024,11.87862885,12.51252812,13.1285205\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.349764816,9.978253691,10.62047137,11.26749401,11.91057246,12.54206169,13.15581583\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.098889784,7.874873766,8.647004556,9.408971799,10.15545223,10.8819456,11.58475119\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.893235923,8.729768549,9.549394387,10.34812708,11.12192211,11.86712385,12.58077165\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.30148611,10.12118284,10.9119357,11.67001833,12.3928161,13.0787243,13.72702154\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,8.098274618,8.915193298,9.71507741,10.49423364,11.24903201,11.97620251,12.6730748\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.170058903,9.994621676,10.78820006,11.54781543,12.27145181,12.95794376,13.60686463\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.869381672,8.699554447,9.512535594,10.30482355,11.07271532,11.81276426,12.52211\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.034288409,7.935384628,8.827596582,9.700457289,10.54586158,11.35784401,12.13232465\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.090564633,7.865988559,8.630552284,9.379972217,10.11096883,10.82077542,11.50700325\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,6.891573757,7.68208457,8.46372837,9.231702853,9.981986854,10.71108218,11.41599186\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.172824707,9.821734718,10.48037052,11.14079775,11.79502125,12.43595386,13.05785384\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.210058513,9.859513296,10.5178054,11.17750337,11.83083845,12.47081676,13.09173206\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.317117275,9.949021161,10.59419619,11.24377487,11.88910046,12.52261231,13.1382261\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.357142016,9.985119102,10.62674678,11.27316217,11.91565256,12.54659393,13.15985166\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.043968936,7.831838002,8.613145072,9.38223948,10.1342784,10.86511974,11.57133445\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.871012357,8.709425207,9.530779494,10.33114499,11.10649187,11.85316116,12.56818366\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.316794328,10.13646337,10.92722703,11.6853328,12.40813842,13.09401852,13.74223953\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,8.129489768,8.943151919,9.740138711,10.51679706,11.2694724,11.99484541,12.69019166\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,9.210130372,10.03016969,10.81982717,11.57605249,12.29675598,12.98070481,13.62741371\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.892631848,8.717396407,9.524984428,10.31216698,11.07541203,11.81136186,12.51718452\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.038406381,7.938578649,8.829960142,9.702119237,10.54694867,11.35846791,12.13257923\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.087767512,7.865125057,8.630838801,9.380976708,10.11246533,10.82265201,11.50920628\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,6.888427246,7.679420485,8.461084835,9.228738031,9.978487584,10.70694395,11.41119084\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.43702471,11.16028467,11.87803671,12.58394139,13.27134362,13.93446901,14.56891058\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.42180691,11.16033415,11.8914986,12.60871877,13.30532632,13.97568329,14.61559997\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.65703057,11.34896307,12.03933687,12.72181982,13.38948995,14.0361584,14.65695254\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.62308839,11.34150595,12.05665091,12.76077068,13.44637855,14.10727293,14.73887826\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.54597095,11.24970086,11.95184687,12.64513583,13.32223781,13.97688615,14.60430793\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.72403768,11.40511133,12.08806509,12.76540784,13.42942073,14.0733828,14.692074\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.78764208,8.592223939,9.390323812,10.17489286,10.93984317,11.68011873,12.39176175\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.35385711,11.08206183,11.80424569,12.51422166,13.20542484,13.87213183,14.50996316\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.45335415,11.18959049,11.9184327,12.63341007,13.32791454,13.99633576,14.63449156\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.62186586,11.31687535,12.01020439,12.69546644,13.36570317,14.01470913,14.63761061\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.56944346,11.29079582,12.00806579,12.71385244,13.40090136,14.06315054,14.69609938\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.51427056,11.22018084,11.92384477,12.61827389,13.29632171,13.9518305,14.58008618\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.71171157,11.39035685,12.07116958,12.74673543,13.40936261,14.05231972,14.67035283\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.702916715,8.51809562,9.325341519,10.11785199,10.88970043,11.63595837,12.35278049\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.4406206,11.16583614,11.88520599,12.59242014,13.28084944,13.94474846,14.57974198\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.38810635,11.129454,11.86298937,12.58226398,13.28069229,13.95268878,14.59409771\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.63866855,11.3335276,12.02661318,12.71155578,13.38140974,14.02998144,14.65240882\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.61608547,11.33566333,12.05177336,12.75670116,13.44298867,14.10445615,14.73654526\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.53686527,11.23989057,11.94143437,12.63424971,13.31101459,13.96545742,14.59279267\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.71380894,11.39465531,12.07740138,12.75458954,13.41851877,14.0624735,14.68123058\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.817590478,8.622378423,9.420399472,10.20458497,10.96888774,11.70831211,12.41896073\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.42985811,11.15365747,11.87211555,12.57878564,13.26694392,13.93077664,14.56585748\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.45921279,11.19433543,11.9225386,12.63716631,13.33148816,13.99981641,14.63792185\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.58224538,11.2802693,11.9762423,12.66386079,13.33622437,13.98716784,14.61184568\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.62215585,11.34258357,12.05905431,12.76400846,13.45010608,14.11125305,14.74295068\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.45761401,11.16552203,11.87129034,12.5678984,13.24816251,13.90589021,14.53633817\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,10.74002052,11.41809926,12.09855915,12.77382286,13.4361061,14.07863402,14.69614036\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,7.752574504,8.567293326,9.373276648,10.16399835,10.9337471,11.67775103,12.39227341\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,16.76651964,17.32157256,17.81566205,18.26099671,18.66623812,19.03765053,19.37985409\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,13.77672471,14.68274485,15.49644591,16.22837921,16.88790088,17.48322361,18.02152958\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.48090762,15.31331683,16.05797517,16.72656892,17.32889187,17.87314332,18.36621761\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.07538369,15.84506312,16.52772853,17.13806324,17.68727655,18.18405335,18.63524418\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.20844389,16.00849733,16.72696875,17.3740224,17.95782076,18.48522353,18.9621761\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.7821112,16.43204059,17.01874546,17.55186273,18.03864445,18.4846819,18.89440656\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.62630481,16.3229432,16.93918936,17.48983091,17.98590308,18.4357566,18.84581041\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,13.66781845,14.61442968,15.46370516,16.22626661,16.9116814,17.52849515,18.08430568\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.87882994,16.54861648,17.13765463,17.66225675,18.13423729,18.56228846,18.95291314\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.33002641,15.18627863,15.95470222,16.64583618,17.26878638,17.83141099,18.3405061\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,13.98867676,14.86809607,15.65517101,16.36165577,16.99764614,17.57174155,18.09125933\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.00509399,15.78793558,16.48098104,17.09953481,17.65529177,18.15731059,18.612728\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.78844078,15.63621483,16.39508595,17.07656773,17.68990583,18.24282146,18.74194542\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.2934748,16.00591669,16.64372658,17.21919607,17.74150141,18.21765268,18.65314514\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,16.11914417,16.75643615,17.32412228,17.83451625,18.29681099,18.71798108,19.10341105\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.62810897,15.45517718,16.2050411,16.88416125,17.49894187,18.05549791,18.55953818\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,16.87527137,17.41459443,17.89636626,18.33187005,18.72912146,19.09393015,19.43059284\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,13.87780803,14.77211957,15.57599703,16.29965186,16.952148,17.54146005,18.07458081\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.63607137,15.45038719,16.1796706,16.8351765,17.42631869,17.96097359,18.44576722\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.93655895,15.72020298,16.41526915,17.03653198,17.59534754,18.10056002,18.5591722\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.9964864,15.81818398,16.5554829,17.2189005,17.81695334,18.35681994,18.84471908\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,16.17025246,16.77337906,17.32094302,17.8210525,18.27977907,18.70179573,19.09081353\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,16.56559405,17.14073945,17.65764958,18.12611938,18.55347173,18.94527178,19.30582654\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.31573377,15.19805635,15.99084683,16.70376867,17.34549819,17.92378561,18.44553411\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,16.43917176,17.03572125,17.56425146,18.03845816,18.4681207,18.86035437,19.22043617\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.27653273,15.13584948,15.90698741,16.60061961,17.2259229,17.7907892,18.30202816\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.37356582,15.2040905,15.95133004,16.62492348,17.2334172,17.78426363,18.28392081\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.11827811,15.88473965,16.56350733,17.16976185,17.71499868,18.20805754,18.65586294\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.83548819,15.67996474,16.4359401,17.11484341,17.72585311,18.27664115,18.7738036\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.22780973,15.94725347,16.5909327,17.17135921,17.69788873,18.1776746,18.61632481\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,15.41874552,16.13857552,16.77506617,17.3432998,17.85463931,18.31775163,18.7393418\n\"linker [N]1C=NN=C1, [O-]C(=O)c1cc(cc(c1C(=O)[O-])C(=O)[O-])N(=O)=O, nodes [Zn], topology \",,,14.16598949,15.0635119,15.86950456,16.5939691,17.24583969,17.8330709,18.36273249\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,20.02634947,20.43146602,20.75699025,21.02179506,21.23965059,21.42074273,21.57270628\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,20.02640333,20.43151135,20.75702898,21.02182857,21.23967986,21.42076853,21.57272919\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,11.07142393,12.02257912,12.91081885,13.73479605,14.49489627,15.19296105,15.83191438\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,11.08546477,12.03311345,12.91917051,13.74182195,14.50113279,15.19873237,15.83740845\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,11.07141217,12.02256523,12.91080396,13.73478089,14.49488132,15.19294659,15.83190057\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,11.08548004,12.03312666,12.91918184,13.74183156,14.50114088,15.19873911,15.83741403\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.373419999,4.115153445,4.863714738,5.602299058,6.319106255,7.006559034,7.660433938\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.158579928,5.546882933,5.96348992,6.402451467,6.856714779,7.319374474,7.784382272\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.05223342,5.449561371,5.872865944,6.316878294,6.775030971,7.240749328,7.708201392\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.702065783,6.087636113,6.499903912,6.932787428,7.379346975,7.832975267,8.28802771\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.163592647,3.80726974,4.475303726,5.151179687,5.821659708,6.476949706,7.110389688\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.366394522,4.106241565,4.85342286,5.591056304,6.307266632,6.994409953,7.648206476\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.14952068,5.538943214,5.956440637,6.396124523,6.850985015,7.314147445,7.779585765\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.04739649,5.445630582,5.86964104,6.314209703,6.772804746,7.238877147,7.70661376\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.690822719,6.077537865,6.490718969,6.924357152,7.371559777,7.825750016,8.28130312\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.163676153,3.807221857,4.475149127,5.150939792,5.82135312,6.476592415,7.109995245\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.373411447,4.115144208,4.863704969,5.602288917,6.319095896,7.006548607,7.660423584\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.15830698,5.546601961,5.9632016,6.402157524,6.856417578,7.319076698,7.784086689\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.052776209,5.450120947,5.873438028,6.317457934,6.775613017,7.241328786,7.708773658\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.701821169,6.087391708,6.499661254,6.932548237,7.37911296,7.832748017,8.287808638\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.163608662,3.807288056,4.47532402,5.151201549,5.82168272,6.476973477,7.110413879\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.366376209,4.106222559,4.853402563,5.591034485,6.307243315,6.994385306,7.648180737\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.149230251,5.53865203,5.956149885,6.39583585,6.850700279,7.313868548,7.779314541\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.047415243,5.44565102,5.86966233,6.314231263,6.772826152,7.238898073,7.706633937\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,5.691076222,6.077796224,6.490980477,6.924619786,7.371821369,7.826008392,8.281556203\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,3.16373734,3.807291151,4.475224717,5.151019911,5.821436174,6.476677038,7.110080316\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,12.60589879,13.25667203,13.86866919,14.44406923,14.9840035,15.48939105,15.96131448\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.86727871,8.631837713,9.381285335,10.11563065,10.83280215,11.52975351,12.20330432\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.563991654,8.438314674,9.294399726,10.1260815,10.92820571,11.69675168,12.42887135\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,9.115454264,9.932856108,10.71819173,11.46891486,12.18330701,12.86040602,13.49992719\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,12.6029448,13.25382066,13.86596617,14.44152914,14.98162499,15.48716523,15.95922938\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.862096919,8.627087719,9.376959797,10.11169912,10.82922557,11.5264918,12.20032004\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.564474427,8.439117015,9.295523871,10.12749609,10.92986375,11.69860186,12.43086442\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,9.117348793,9.934724905,10.72007083,11.47081692,12.18523128,12.86234474,13.5018695\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,12.60593289,13.25670204,13.86869583,14.44409312,14.98402514,15.48941085,15.9613328\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.867276821,8.631838787,9.381288702,10.11563577,10.83280861,11.52976098,12.20331254\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.564003522,8.43832642,9.294411815,10.12609413,10.92821892,11.69676541,12.42888549\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,9.115490359,9.932889072,10.71822194,11.46894262,12.18333253,12.86042951,13.49994884\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,12.60297399,13.25384296,13.86598324,14.44154219,14.98163495,15.48717278,15.95923504\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.862104452,8.627091899,9.376960817,10.11169727,10.82922118,11.52648523,12.20031164\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,7.564498544,8.439138895,9.295543504,10.12751354,10.92987916,11.69861537,12.43087622\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,9.117317255,9.934697934,10.72004807,11.47079795,12.18521566,12.86233205,13.50185933\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.33768087,15.22308305,16.0131641,16.72036018,17.35456991,17.92404684,18.43591785\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.45812473,15.31629481,16.08532111,16.77606776,17.39734787,17.95663016,18.46045282\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,15.59685213,16.35612063,17.03404543,17.63944497,18.18006888,18.66295804,19.09455804\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.63512357,15.48861176,16.25209637,16.93675008,17.55157498,18.10418313,18.60123437\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.62082202,15.46394701,16.22015126,16.89976175,17.51122983,18.06177544,18.55776016\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,15.6515011,16.40436188,17.07694271,17.67782336,18.21458722,18.69415325,19.12287419\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.3390767,15.22432527,16.01427393,16.72135584,17.35546684,17.92485806,18.43665434\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.45807217,15.31623553,16.08525925,16.7760058,17.39728726,17.95657174,18.46039701\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,15.5965724,16.35587592,17.03382989,17.63925392,18.17989859,18.66280545,19.09442066\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.63546715,15.48890577,16.25235047,16.9369717,17.55176984,18.10435573,18.60138827\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,14.62084356,15.4639563,16.22015142,16.89975514,17.51121828,18.06176035,18.55774261\n\"linker Cc1cc(c(cc1P(=O)(O)[O])C)P(=O)([O])O, nodes [Mn], topology pcu\",,,15.65139443,16.40426215,17.07685069,17.677739,18.21451008,18.69408273,19.12280966\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,19.1111991,19.40755745,19.64811395,19.84543348,20.00889861,20.14557963,20.26085605\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,3.137046283,3.820453096,4.52461247,5.231589571,5.927633526,6.603029105,7.251538048\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,2.971564382,3.666088401,4.381276083,5.098630352,5.804206196,6.488277777,7.144673365\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,3.197779822,3.747526801,4.326231963,4.921451293,5.522112563,6.119168062,6.705744865\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,2.909127235,3.589111437,4.293904593,5.004345104,5.705769709,6.387793463,7.043686329\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,2.404918553,3.006604809,3.647801436,4.309907677,4.977445053,5.638454401,6.284314045\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,3.383226487,4.056611925,4.74649547,5.436740428,6.115002974,6.772573937,7.403874861\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,3.13638268,3.819803264,4.523978083,5.230971381,5.927032022,6.602444731,7.250971229\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,2.971902526,3.666494209,4.381735692,5.099130734,5.804735583,6.488825913,7.145231585\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,3.193372323,3.742796452,4.321296784,4.916426993,5.517108217,6.114285688,6.701080407\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,2.909681896,3.5897168,4.29455124,5.005023856,5.706471859,6.388511012,7.044412163\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,2.404640263,3.006413119,3.647701603,4.309900163,4.977525834,5.638616062,6.284547044\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,3.383543223,4.056967205,4.746856859,5.437087158,6.115323191,6.772862066,7.404129474\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.737595448,9.55762531,10.33925467,11.08242316,11.78737569,12.45455127,13.08458038\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,10.94924684,11.82555978,12.58530685,13.24721322,13.82876116,14.34513798,14.80896135\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,9.088235127,9.90940079,10.68990668,11.43034092,12.13123482,12.79317654,13.41691396\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,7.077310021,7.844794843,8.60371429,9.350118247,10.07994731,10.78930789,11.474764\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,7.017918958,7.797507543,8.565558217,9.319283683,10.05532725,10.77017491,11.46057375\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.751860481,9.465495293,10.1677981,10.85416559,11.52031039,12.16262643,12.77835677\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,9.263925754,10.04566467,10.79646204,11.51508257,12.20022658,12.85090655,13.46661891\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.800561052,9.597549864,10.36854525,11.11049232,11.82066329,12.49695978,13.13804607\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.780645727,9.579688931,10.34814503,11.08403278,11.78580822,12.45246626,13.08356678\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.738837371,9.558873616,10.34049535,11.083647,11.78857628,12.45572397,13.08572182\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,10.94889903,11.82515063,12.5848617,13.24675653,13.82831442,14.34471884,14.80858348\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,9.081529739,9.903358254,10.68446239,11.4254306,12.12679829,12.78915928,13.4132674\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,7.078695468,7.846014469,8.60477636,9.351036388,10.08073716,10.7899852,11.47534366\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,7.018706677,7.79812104,8.566050567,9.319691049,10.0556749,10.77048071,11.46085036\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.752249793,9.465918575,10.16820589,10.85453201,11.52062462,12.16288718,12.77856865\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,9.262934515,10.0446157,10.7953653,11.51395369,12.19908237,12.84976245,13.46548777\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.798646245,9.596033577,10.36733356,11.10951427,11.81986546,12.49630198,13.13749799\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,8.77795434,9.577163177,10.34573702,11.08171671,11.78357164,12.45030414,13.08147782\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,10.7852628,11.51592721,12.21920243,12.89381269,13.53812622,14.15070963,14.73060715\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,14.26716672,14.96326156,15.56672504,16.0972717,16.56965163,16.99488709,17.38125341\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,11.66567785,12.4372642,13.14623971,13.80152808,14.40977061,14.97589587,15.50364894\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,10.76621743,11.49729832,12.20109679,12.8763171,13.52130366,14.13459998,14.71523011\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,14.21174425,14.91517182,15.52477556,16.0604728,16.53718906,16.96609254,17.35557781\n\"linker N#C[N]c1ccc(cc1)[N]C#N, n1ccc(cc1)c1ccncc1, nodes [Mn], topology sql,pcu\",,,11.71829244,12.48339994,13.18704854,13.83793009,14.44249685,15.0055272,15.53064859\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,21.14357584,21.32265658,21.46231588,21.57322271,21.6627029,21.73590761,21.79653757\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,21.11765921,21.26744515,21.38323814,21.47455607,21.54782035,21.60748379,21.65670976\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,20.87386336,21.03066048,21.15212868,21.24806964,21.32513059,21.38793932,21.43979364\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,21.12683884,21.30598515,21.44569579,21.55664361,21.64615706,21.71938916,21.78004197\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,21.11949175,21.26925463,21.38502927,21.47633249,21.54958487,21.60923859,21.65845656\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,20.88139663,21.0381302,21.15954785,21.25544803,21.33247565,21.39525678,21.44708803\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.715915308,4.398963105,5.100615678,5.802264557,6.490154534,7.15489023,7.790673518\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.67687054,4.352232671,5.047823499,5.744950117,6.429682095,7.092416154,7.727146434\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.716370404,4.39942593,5.101072541,5.802707913,6.490580673,7.155297767,7.791062421\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.67762936,4.353009889,5.048615408,5.745753659,6.430494504,7.093234876,7.727969131\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.716672731,4.39974254,5.10139625,5.80303328,6.490903787,7.155615952,7.791373945\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.678096659,4.353491427,5.049104583,5.746245292,6.430984751,7.093721008,7.728449302\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.716162935,4.399222227,5.10088214,5.802534991,6.490426299,7.155161313,7.790942422\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.677089083,4.352438594,5.048017566,5.745133751,6.429857074,7.092584363,7.727309689\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.318051193,3.962782866,4.639086354,5.326757223,6.010011626,6.677432116,7.321416541\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.746418762,4.427582351,5.12758811,5.827793903,6.514435361,7.178120316,7.813058002\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.319791482,3.964617915,4.641004263,5.328743929,6.012052378,6.679512614,7.323523692\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,3.74640285,4.427528892,5.127492431,5.827656688,6.514260478,7.177913206,7.812824609\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.170409599,9.787178788,10.42160725,11.06358636,11.70353341,12.3332125,12.94605563\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.149704651,9.764481305,10.3971186,11.03747796,11.67593229,12.30420587,12.91570177\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.171066527,9.788094754,10.42272944,11.06487646,11.704963,12.33476007,12.94770464\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.156638848,9.771456031,10.40411162,11.04447281,11.68291651,12.31116996,12.92263861\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.171665912,9.788737435,10.42340758,11.06558453,11.70569712,12.33551746,12.94848331\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.158415498,9.773269991,10.40596016,11.0463532,11.68482605,12.31310608,12.92459884\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.171249606,9.788057237,10.42251782,11.0645246,11.70449614,12.33419731,12.94706066\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.151736924,9.766514481,10.39915263,11.03951302,11.67796871,12.30624409,12.91774223\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.218552967,9.818223512,10.43958424,11.07198771,11.70522933,12.33047448,12.94063192\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.437402159,10.05352382,10.68730328,11.3283692,11.96699337,12.59488301,13.2054753\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.227689405,9.827430816,10.44886427,11.08134194,11.71465812,12.33997691,12.95020588\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,9.43853836,10.05479251,10.68864204,11.3297359,11.96836062,12.59623392,13.2068003\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.71366228,11.39607613,12.08279161,12.76402736,13.43078376,14.07576106,14.69360293\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.714616,11.3974474,12.08472067,12.76642753,13.43346084,14.07848639,14.69615447\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.8400577,11.49712261,12.15869987,12.81609738,13.46103122,14.08657737,14.68749312\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.71119592,11.39447071,12.08186621,12.76364995,13.43085593,14.07620792,14.69436641\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.71407962,11.39785767,12.08589986,12.76823997,13.43580083,14.08127025,14.69931501\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.84632383,11.50317162,12.16454957,12.82176809,13.46654372,14.09195156,14.69274737\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.71228951,11.39559769,12.08301946,12.76482341,13.43204461,14.07740782,14.69557439\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.71618145,11.39989413,12.08788091,12.77017351,13.43769322,14.08312663,14.70113958\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.84831028,11.50519562,12.16660395,12.82384767,13.46864465,14.09407089,14.69488276\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.71475387,11.39721284,12.08396404,12.76522811,13.43200707,14.07700245,14.69485892\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.71656669,11.3993603,12.08659985,12.76827621,13.43528168,14.08028164,14.69792611\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.8421399,11.49924826,12.16086145,12.81828927,13.46324911,14.08881783,14.68975341\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.86602626,11.56422117,12.26429337,12.95600109,13.63032389,14.28020124,14.90064129\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.89809636,11.58362981,12.27431636,12.95953076,13.62978401,14.27753717,14.89735787\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,11.02077466,11.6843992,12.35153999,13.01346921,13.66192997,14.29007097,14.89275013\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.87659503,11.57497938,12.27518871,12.96699452,13.64138534,14.2913071,14.91177288\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,10.8903583,11.57685983,12.26833781,12.95421063,13.62502078,14.27325216,14.89348905\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,11.02712848,11.69068575,12.35776189,13.01963342,13.66804559,14.29614771,14.89879731\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,20.62127904,20.84808465,21.02648791,21.1690023,21.28444738,21.37914784,21.45771618\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,22.10994458,22.37663027,22.58366975,22.74737551,22.87891284,22.98610817,23.0745667\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,21.36271571,21.59797241,21.78035944,21.92441759,22.04007007,22.13425639,22.21193726\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,20.65824493,20.88541354,21.06409636,21.20683044,21.32245117,21.41729423,21.49597986\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,22.12601136,22.39238069,22.59917228,22.76268063,22.89405846,23.00112323,23.08947364\n\"linker [N]1C=NN=C1, nodes Cl[Cd], Cl[Cd]Cl, [Cd], topology pcu\",,,21.39233474,21.62736801,21.80957684,21.9534912,22.06902634,22.16311584,22.24071603\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,20.79995879,21.20929114,21.53380914,21.79496517,22.00795275,22.18374176,22.33039261\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,20.5066671,20.96278023,21.32404919,21.61450435,21.8511724,22.04634275,22.20903885\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,20.78894696,21.19993993,21.52578478,21.78801364,22.00187861,22.1783929,22.32564928\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,20.51960069,20.97372343,21.33341386,21.62259977,21.85823421,22.052553,22.21454005\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,2.717638803,3.37566166,4.062932731,4.760823191,5.454572179,6.13334684,6.789816338\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.210132742,3.909593377,4.622483202,5.332739241,6.028332045,6.7009296,7.345316099\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.109032365,3.746705387,4.409287405,5.080277527,5.746512558,6.398249036,7.028825954\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.48879136,4.161083488,4.848490141,5.535567364,6.210409603,6.86455055,7.49252611\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.503242949,4.160945993,4.837890099,5.517942462,6.188472794,6.840374556,7.467666054\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.165530944,3.813201243,4.484427346,5.162597694,5.834544627,6.490608198,7.124270803\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.039691778,3.721844745,4.42362649,5.127998595,5.821897136,6.496051899,7.144460354\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,2.797476812,3.464863246,4.158410557,4.85991652,5.555145104,6.233779951,6.88894655\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.267078337,3.918961573,4.592294201,5.270812315,5.941733795,6.595764715,7.226706539\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.554267878,4.223117357,4.908270668,5.593920294,6.267839122,6.921322353,7.548751051\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.56686662,4.235029784,4.917502237,5.599282899,6.268786036,6.91776231,7.540884938\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.188070163,3.836320707,4.506569546,5.182653575,5.851834857,6.504805751,7.135308775\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,2.717927293,3.375892055,4.063103577,4.760937358,5.454635003,6.133364784,6.789796117\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.210309094,3.909828704,4.622771613,5.333073265,6.028703533,6.701330424,7.34573863\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.109813919,3.747463624,4.410018325,5.080978664,5.74718269,6.398887897,7.029433991\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.489447689,4.161855506,4.849343688,5.536473494,6.211344871,6.865496557,7.49346876\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.502469629,4.160133842,4.837065864,5.517125046,6.187675007,6.839604654,7.466928982\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.164600232,3.812202246,4.483378463,5.161516792,5.833447708,6.489508821,7.123179972\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.040063643,3.722208677,4.423982961,5.128347348,5.822237479,6.49638297,7.144781302\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,2.798466131,3.465921467,4.159510298,4.86103425,5.556261917,6.234881459,6.890022335\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.267070722,3.918946313,4.592272094,5.270783878,5.94169949,6.595725042,7.226662046\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.553454653,4.222251059,4.907370234,5.59300257,6.26691824,6.920409704,7.547855557\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.566180989,4.234310701,4.916764802,5.598540628,6.268050432,6.917042966,7.540189836\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,3.188092385,3.836328546,4.506561702,5.182630301,5.851797303,6.504755548,7.135247755\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.155503296,8.004536763,8.840128229,9.656317941,10.4480887,11.21135017,11.94296429\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.295561744,8.119695404,8.925055408,9.709555416,10.47071975,11.20594946,11.91284682\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.154405035,7.989242623,8.807039199,9.60460422,10.37870702,11.12626237,11.84458601\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.063299629,9.957635534,10.79930685,11.59058197,12.3337839,13.03112331,13.68471079\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.331080484,7.134997282,7.943352221,8.746838835,9.537534967,10.3088659,11.05558769\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.307324075,7.114111994,7.922757869,8.724782328,9.513008322,10.28144002,11.02523761\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.230989901,8.075931528,8.906123621,9.716288325,10.50189775,11.25918192,11.98519291\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.385507617,10.1754981,10.93049038,11.6506503,12.33609779,12.98698242,13.60358205\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.293556488,10.17227843,10.99785754,11.77349798,12.50200737,13.18580627,13.82705737\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.49477777,10.28222036,11.03635267,11.75680889,12.44318546,13.09520171,13.71282281\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.83461254,10.57546263,11.28783699,11.97137728,12.6254574,13.24944779,13.84290398\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.533894994,10.31511905,11.06345047,11.77856115,12.46010901,13.10785326,13.72176677\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.176166787,8.016927779,8.843871982,9.651561599,10.43536952,11.19145472,11.91680813\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.215431583,8.044044757,8.853394913,9.641315624,10.40539351,11.14313915,11.85226476\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.256441182,8.07993603,8.884702334,9.668665779,10.42940119,11.16435733,11.87116668\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.207637957,10.09323661,10.925529,11.70743983,12.44166943,13.13062246,13.7764907\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.319790391,7.114056716,7.910282821,8.700449321,9.477756064,10.23646427,10.97187005\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.373478723,7.158823238,7.947671351,8.731688232,9.503848102,10.25824057,10.99002496\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.161873924,8.003957396,8.832691938,9.642351961,10.42812218,11.1860495,11.91306617\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.413414615,10.20848934,10.96796273,11.69201637,12.38075487,13.03432045,13.65300419\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.213533506,10.09413237,10.92272459,11.70191648,12.43415024,13.12163829,13.76643411\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.447134376,10.23086075,10.98092292,11.69720841,12.3795833,13.02798826,13.64253931\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.6259649,10.39587305,11.13377799,11.83948819,12.51268367,13.1530846,13.760593\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.72953296,10.48666538,11.2129917,11.90837655,12.57246819,13.20490718,13.80549263\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.155584456,8.004694988,8.840342543,9.656573825,10.44837568,11.2116603,11.94329129\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.294951027,8.119070611,8.924417705,9.708906923,10.47006341,11.20528868,11.91218521\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.155115662,7.98990007,8.807649821,9.605174612,10.3792431,11.12676908,11.84506723\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.062882762,9.957302992,10.79904398,11.59037593,12.33362391,13.0310006,13.68461822\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.332780007,7.136258492,7.944298108,8.747559156,9.538094522,10.30931108,11.05595149\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.305580777,7.112747809,7.921702776,8.723979111,9.512409926,10.28100768,11.02493944\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.229439616,8.074315879,8.904481036,9.714644659,10.50027083,11.25758419,11.98363311\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.384813443,10.174827,10.9298352,11.65000682,12.33546402,12.98635791,13.60296731\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.293108215,10.17178542,10.99733412,11.77295656,12.50145811,13.18525718,13.82651455\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.495443559,10.28279632,11.0368555,11.75725129,12.44357731,13.09555089,13.71313569\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.836370207,10.57705596,11.28928948,11.97270774,12.62668111,13.25057731,13.84394981\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.532608375,10.31397238,11.06242676,11.77764536,12.45928794,13.1071154,13.72110206\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.176665953,8.017454499,8.844400684,9.652076625,10.43586184,11.19191962,11.9172437\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.215954114,8.044491875,8.853759635,9.641597604,10.40559672,11.14327013,11.85233136\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.257147925,8.080549963,8.885219055,9.669087115,10.42973287,11.16460731,11.87134393\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.2085395,10.09406227,10.92628505,11.70813244,12.44230442,13.13120527,13.77702631\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.320404282,7.114488347,7.910544879,8.700555802,9.477722664,10.23630782,10.97160771\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,6.370764916,7.156714542,7.94600692,8.730347434,9.502741371,10.25730222,10.98920745\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,7.16215271,8.004204798,8.832916053,9.642558129,10.4283139,11.1862291,11.91323522\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.413481408,10.20859226,10.96808712,11.69215267,12.38089675,13.03446371,13.65314603\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.215274981,10.09571562,10.92416369,11.70322635,12.43534516,13.12273126,13.76743664\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.447904119,10.23157656,10.98158811,11.6978269,12.38015903,13.02852494,13.64304034\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.625542969,10.39550675,11.13345145,11.8391913,12.51240996,13.1528299,13.76035458\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,9.729586363,10.48674424,11.21308521,11.90847754,12.57257198,13.20501075,13.8055941\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.84157569,14.71530718,15.49243113,16.1872395,16.81140208,17.37443306,17.88412598\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.08189179,15.01027272,15.82963187,16.55668675,17.20480458,17.78479474,18.30552469\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.42471907,15.25660384,15.99260076,16.64808256,17.235338,17.76417635,18.24247167\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.74161188,14.72272056,15.58844385,16.35561781,17.03808061,17.64725229,18.19264198\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.67896865,14.60144296,15.42135227,16.1530512,16.80853588,17.39777626,17.9290827\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.83350482,15.6412835,16.35587803,16.99238483,17.5626686,18.0761179,18.54025377\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.60274531,14.54663908,15.38177241,16.12424525,16.78733569,17.3819365,17.91701605\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.38070238,15.23289544,15.98640177,16.65716062,17.25770803,17.79798016,18.28595299\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.81687294,14.69359774,15.47324365,16.1701839,16.7961578,17.36073676,17.87176071\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.07411595,15.00336748,15.82345364,16.55112258,17.19976497,17.78020791,18.30133223\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.40198503,15.23595533,15.97383346,16.63099752,17.21975125,17.74992236,18.22940369\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.79060332,14.76716439,15.62878124,16.39228462,17.07148148,17.67775149,18.22056231\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.64665161,14.57228242,15.39491134,16.12896669,16.78650664,17.37755169,17.91045289\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.80685429,15.6183051,16.33585262,16.97476893,17.54704515,18.06216196,18.52770852\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,13.60741013,14.55075246,15.38538792,16.12741919,16.79012221,17.38438534,17.91917172\n\"linker [O-]C(=O)c1ccc(c2c1cccc2)C(=O)[O-], nodes [Zn], topology \",,,14.39485537,15.24557884,15.9977982,16.66743213,17.26699576,17.80640598,18.2936217\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,17.86008709,18.32265972,18.68937753,18.98439011,19.22489498,19.4233315,19.58883983\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,17.76946732,18.2448906,18.62210175,18.925739,19.17338747,19.37778864,19.54831704\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.642406169,4.364940917,5.094581054,5.81451269,6.512867878,7.181983686,7.817541054\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.661520782,4.384074824,5.113742816,5.833709395,6.532103339,7.201258783,7.836854629\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.654643081,4.377344423,5.107068445,5.827015897,6.525331836,7.194364928,7.829806325\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.665257579,4.38799146,5.117743417,5.837714274,6.536049651,7.205099222,7.840555239\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.645387304,4.367924659,5.097564494,5.81749425,6.515846809,7.184959743,7.820514286\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.660573937,4.383134793,5.112810408,5.832784355,6.5311848,7.200345595,7.835945567\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.651677125,4.374376715,5.104100709,5.824049061,6.522366349,7.191400953,7.82684386\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,3.666192327,4.388910373,5.118646831,5.838603698,6.536927166,7.205967073,7.8414156\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.216384792,8.941139021,9.657058482,10.3584318,11.03985638,11.69680104,12.32584254\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.287369753,9.012561407,9.728749421,10.43029115,11.11182396,11.7688403,12.39793106\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.251248731,8.976484648,9.692748738,10.3943733,11.07598675,11.7330796,12.36224344\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.284634442,9.009589687,9.725551167,10.42688977,11.10824928,11.76512405,12.39410414\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.225389436,8.950182815,9.666134141,10.36753359,11.04897975,11.70594232,12.33499881\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.284713219,9.009884663,9.726056477,10.42758562,11.10910885,11.76611795,12.39520327\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.242008527,8.967225092,9.683475618,10.38509062,11.06669738,11.72378563,12.35294644\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,8.287384586,9.012385363,9.728382989,10.42974994,11.11113143,11.76802308,12.39701599\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,7.59636788,8.321202041,9.039381547,9.748109056,10.44377469,11.1225316,11.78077234\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,7.587046537,8.312762433,9.031737046,9.741183356,10.4374976,11.11683797,11.77560205\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,7.596349186,8.32118973,9.039373693,9.748104281,10.44377204,11.12253043,11.78077221\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,7.587063599,8.312761105,9.031720867,9.74115537,10.43746038,11.11679365,11.77555241\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.29630466,10.0871684,10.86041164,11.61085616,12.3332814,13.02335758,13.6780178\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.307247559,10.10356632,10.88126571,11.63538513,12.36086807,13.05350983,13.71033978\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.320470829,10.11364549,10.88876226,11.64073167,12.36440789,13.05552152,13.71105304\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.282811027,10.08158188,10.86143926,11.61746645,12.34464531,13.03880301,13.69699483\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.299467242,10.090398,10.86369872,11.61419381,12.33666442,13.02678185,13.68147992\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.306096511,10.10252038,10.88031299,11.63451414,12.36006801,13.05277083,13.70965302\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.316988373,10.1099528,10.88489253,11.63671261,12.36026256,13.05126911,13.70670948\n\"linker N1=C[C](C=N1)C1=C[N]N=C1, nodes [Cu], topology lvt\",,,9.283002228,10.08186961,10.86181581,11.61792578,12.34518255,13.03941403,13.69767593\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,20.92771012,21.0529424,21.15038897,21.22763539,21.28986296,21.34070284,21.38275784\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,20.87424012,21.03909218,21.16778641,21.27006272,21.35262231,21.42018733,21.47615704\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,20.57367413,20.72585803,20.84492048,20.93971534,21.01635136,21.07914576,21.13121502\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,3.749176834,4.481175635,5.227456697,5.967750011,6.687539958,7.377376415,8.031869228\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,2.225275916,2.750648438,3.335140113,3.960975307,4.611775603,5.273871161,5.936628978\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,3.311608511,4.000066531,4.711126925,5.42508759,6.127069243,6.806752579,7.45767058\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,4.687183885,5.475608782,6.248382488,6.990722234,7.693467413,8.351710478,8.963585274\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,4.542285194,5.290515499,6.036646143,6.764114367,7.461606878,8.122114328,8.741911135\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,2.889031475,3.506041154,4.164983201,4.845276064,5.529853279,6.205772225,6.863991022\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,4.901732525,5.512836673,6.083402598,6.610503067,7.093744799,7.53444027,7.934942482\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,3.926590798,4.67151094,5.422323494,6.160695125,6.87389331,7.553960665,8.196687633\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,6.932361531,7.763472765,8.579373671,9.373028962,10.13991537,10.87706403,11.5825438\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.847962463,8.610570714,9.377927887,10.14134085,10.8924794,11.62411613,12.33048322\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,9.626246197,10.34889524,11.06063159,11.7554876,12.4281837,13.07451279,13.69145364\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,9.601096269,10.32115078,11.02519587,11.70972751,12.37127612,13.00688113,13.6143218\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.932539619,8.648551589,9.36595785,10.07937267,10.78303457,11.47145365,12.13985309\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,6.922501467,7.688773625,8.45991207,9.226951371,9.982451438,10.72023178,11.4352985\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.368994921,9.341269913,10.25764632,11.11346156,11.90911683,12.64759051,13.33292673\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.099809874,8.86990164,9.63660331,10.39248028,11.13090219,11.84634365,12.53451813\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.46376303,9.185392123,9.891356256,10.57751767,11.24024193,11.8766055,12.48447974\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.006730464,8.726548281,9.438047452,10.13377647,10.80776117,11.45548325,12.07377693\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.653389047,8.33518658,9.017513544,9.696585347,10.36788635,11.02678726,11.66901648\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,6.748354527,7.513314106,8.276462722,9.031034939,9.77169818,10.49401237,11.19427135\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.241981289,8.078051764,8.905543915,9.715858801,10.50258765,11.26097086,11.98759383\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.13495357,8.920095306,9.711152948,10.49754315,11.26951672,12.01894731,12.73962671\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,9.895332063,10.60546195,11.30010261,11.97459029,12.62506518,13.24856096,13.84299801\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,9.840649113,10.53722265,11.21590051,11.87463777,12.51103333,13.12284184,13.70826191\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.246023944,9.019072728,9.795707971,10.56582683,11.32057095,12.05272917,12.75684584\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.253953316,8.055510811,8.848647883,9.626682135,10.38449541,11.11803735,11.82414026\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.118899365,7.922926717,8.707649577,9.468957416,10.20445021,10.9125627,11.59218208\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.313436872,9.079655024,9.847319057,10.60759644,11.35240583,12.07499487,12.7701607\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,8.185069819,8.999526992,9.786827587,10.54257994,11.26354255,11.9475238,12.59330376\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,9.638612043,10.41140676,11.16796142,11.90112551,12.6051215,13.27579854,13.9105747\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.51499954,8.293651291,9.077219355,9.855561324,10.61957971,11.3617245,12.07618773\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,7.135456718,7.927048992,8.706798114,9.469331012,10.21078622,10.92815503,11.61903817\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,10.90605135,11.46413312,11.96716789,12.42351092,12.84002811,13.22220804,13.57438876\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.16868357,15.88967673,16.54028376,17.12886717,17.66234279,18.14654712,18.58651251\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,11.73570644,12.62382734,13.47034486,14.26770924,15.01168903,15.70082842,16.33574523\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.94645881,16.5944623,17.18070535,17.71294166,18.19749444,18.63958025,19.04357891\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.56292273,16.29560965,16.95146151,17.54093671,18.07240012,18.55271708,18.98765425\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,16.81997316,17.79808091,18.61628858,19.30398888,19.88519349,20.37927424,20.80178384\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.62141317,16.12608403,16.57011532,16.96510975,17.32048489,17.64363137,17.94020879\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,11.83571946,12.7411631,13.60583201,14.41991676,15.17816265,15.878818,16.5225976\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.39418562,16.11078051,16.75846172,17.34470298,17.87604761,18.35822194,18.7962623\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,14.81241051,15.46732373,16.06230842,16.6039578,17.09808996,17.54972771,17.96318925\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.49451877,16.21287554,16.85230886,17.42557127,17.94240982,18.41039858,18.83555736\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.63011627,16.27529616,16.85724524,17.38488374,17.86503494,18.30308708,18.70344321\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,12.10248172,13.045663,13.93273983,14.75776873,15.5186371,16.21605202,16.85259697\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,16.31185819,16.91738521,17.45711482,17.94317143,18.38430296,18.78694372,19.15594953\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.44371423,16.18154666,16.84093986,17.43317916,17.9672079,18.4502343,18.88819104\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.03206087,15.76905228,16.42786449,17.01998213,17.55448177,18.03863151,18.47836279\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.63473945,16.20817703,16.72102018,17.18414288,17.60574921,17.99202397,18.34766123\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,10.44018437,11.39418252,12.29013087,13.12249264,13.8895288,14.59224027,15.23342629\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,15.61598658,16.30091512,16.91064171,17.45781444,17.95198535,18.40047421,18.80901057\n\"linker [O-]C(=O)c1ccc(o1)C(=O)[O-], nodes [Cd], topology sxd\",,,16.0684517,16.66226143,17.19665986,17.68117275,18.12295848,18.52747534,18.8989818\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,21.26142317,21.58368625,21.84195195,22.05164441,22.22390992,22.36694175,22.48685483\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,21.17694863,21.49639257,21.75292212,21.96161212,22.1333652,22.27620742,22.39614009\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,21.43625901,21.7326189,21.96918009,22.16063192,22.3175012,22.4474709,22.55624088\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,21.26381031,21.5856062,21.84350476,22.052904,22.22493192,22.36776876,22.48751996\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,21.17651498,21.49637972,21.75325503,21.96223123,22.13422303,22.27726589,22.39736846\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,21.43491055,21.73205548,21.96923493,22.16118147,22.3184522,22.44875178,22.55779588\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.572560394,5.942597766,6.342177886,6.764784272,7.203139274,7.650312643,8.100333373\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.320415523,5.690390539,6.090817258,6.515160659,6.956080563,7.406546164,7.860458476\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.296735478,5.655680914,6.046988185,6.46424412,6.900072852,7.347304435,7.799647846\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,4.652086807,5.361712788,6.042784216,6.69319771,7.311744597,7.89773926,8.450932029\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,4.157663063,4.888408504,5.598473942,6.281486205,6.933481078,7.552103018,8.136164876\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.291522953,5.668978951,6.075772698,6.505669623,6.951535858,7.40646024,7.864404222\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.49406007,5.856292259,6.249819556,6.668004875,7.103404048,7.548889139,7.998279079\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.54665533,5.920972932,6.324742726,6.751254509,7.193122747,7.643373232,8.096034351\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.333734515,3.827213912,4.35291377,4.901409231,5.463001775,6.028917435,6.591913026\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.485533184,3.98694658,4.518982621,5.072178197,5.636905852,6.204558726,6.768120864\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.294960891,3.95102233,4.633303901,5.323037106,6.005651156,6.6707123,7.311387997\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.438658475,4.074917667,4.735559336,5.404016316,6.066986611,6.714641349,7.3403244\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.297342222,3.958521311,4.645481295,5.339270496,6.025226091,6.692884311,7.335421838\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.485579968,3.983604676,4.513483325,5.065623687,5.630221253,6.198478176,6.763196898\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.467144731,3.961259612,4.487507416,5.036357173,5.598060755,6.163845714,6.726505176\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.615356441,5.983861194,6.383203693,6.806346563,7.245623399,7.69383915,8.144857558\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.332457552,5.697610909,6.09498963,6.517882879,6.958720186,7.410227842,7.866081252\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.321115121,5.680942367,6.072955496,6.490718742,6.926863251,7.374226911,7.826517627\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.218906186,5.609778945,6.027130049,6.465526068,6.918386749,7.379195587,7.842201733\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.282740939,5.671810188,6.087627071,6.524696882,6.976368275,7.436083774,7.898085261\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.5391453,5.928049297,6.342179515,6.776107686,7.223301853,7.677366753,8.13273072\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.573083921,5.94317032,6.342790767,6.76543132,7.203816096,7.65101614,8.101061422\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.320976458,5.690966506,6.091402737,6.515752505,6.956677166,7.407146905,7.861063366\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.296908838,5.655897772,6.047239322,6.464522982,6.900374938,7.34762688,7.799989103\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,4.652293308,5.361949719,6.043045406,6.693477582,7.312038294,7.898042656,8.451241692\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,4.156824679,4.887566156,5.597644667,6.280680687,6.932705631,7.551361039,8.135457849\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.292046165,5.669492208,6.076277819,6.506168166,6.95202918,7.406949521,7.864890478\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.494768048,5.856984693,6.250499024,6.668673341,7.104063083,7.549540035,7.998922912\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.547665782,5.922000028,6.325784734,6.752309406,7.194188467,7.644447811,8.097116012\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.335296744,3.828698954,4.354332761,4.902773478,5.464322165,6.030204011,6.593174738\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.487442533,3.988820522,4.520827807,5.073999747,5.638707685,6.20634384,6.76989155\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.29493762,3.950990381,4.633267083,5.322998365,6.005612676,6.670675643,7.311354241\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.438308696,4.074603198,4.735273279,5.403752457,6.066739556,6.714406549,7.340098103\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.297627161,3.958804425,4.645763508,5.339551827,6.025506109,6.693162422,7.335697444\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.485847964,3.983845668,4.513699568,5.065818601,5.630398806,6.198642457,6.763351834\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,3.467698183,3.96184134,4.488109922,5.036973501,5.598684706,6.164471961,6.72712928\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.615982893,5.984428636,6.383715818,6.806802064,7.246015709,7.694156521,8.145083632\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.335646475,5.700796518,6.098166718,6.521033898,6.961817636,7.413236526,7.86896052\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.318580157,5.678366512,6.070348462,6.488091813,6.92422617,7.3715859,7.823874535\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.218614655,5.609492793,6.02684624,6.465243322,6.91810493,7.378915247,7.841923789\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.282720998,5.671813638,6.087646425,6.524726663,6.976404518,7.436123666,7.898126859\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,5.539053454,5.928001308,6.342165534,6.776119778,7.223333573,7.677412875,8.132787029\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,12.72804078,13.32751381,13.89855894,14.44006236,14.95120759,15.4317328,15.88196844\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.696592381,8.387246569,9.072587365,9.752460924,10.4244239,11.0848493,11.72980809\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.270431449,8.027467371,8.78026549,9.524260817,10.25446261,10.9660811,11.65494557\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.492783956,8.197765241,8.900171079,9.59857359,10.28957711,10.96887139,11.6320577\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,12.73160496,13.3481315,13.9349641,14.4908712,15.01501131,15.50716887,15.96776399\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,8.6757363,9.568966689,10.43153681,11.25393481,12.03061505,12.75900194,13.43864172\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.409695446,8.164728103,8.915760007,9.659222354,10.39039476,11.10431997,11.79646571\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.708409066,10.42333851,11.12190348,11.79988238,12.45361706,13.0802705,13.67788436\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.821039925,10.55305652,11.26130956,11.94309044,12.5964941,13.22022032,13.81349093\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.83985118,10.56146754,11.26529411,11.94749592,12.60469626,13.23425849,13.83436453\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.576198361,8.334408107,9.087709511,9.832732152,10.5649524,11.27958148,11.97221843\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.200341592,10.09394041,10.95655043,11.7787377,12.55500303,13.28280537,13.96172113\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,13.1310138,13.74037886,14.31861679,14.86541543,15.38048955,15.86394247,16.31636271\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.974377836,8.676250497,9.370627403,10.05770384,10.73537833,11.40032106,12.04884653\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.683483617,8.447571029,9.20608708,9.954717723,10.6885925,11.40298587,12.09377849\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.716778203,8.433348692,9.145794053,9.852657829,10.55061814,11.23548915,11.90301976\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,12.8793125,13.5140178,14.1149091,14.68191465,15.21498327,15.71444918,16.18112215\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,15.53536487,16.1840821,16.71925211,17.1683773,17.55255648,17.88779768,18.18610682\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,15.69007036,16.31658692,16.83118531,17.26144942,17.62844288,17.94808845,18.2322927\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,15.24724296,15.91817102,16.47475057,16.9433432,17.34460343,17.69448904,18.00516845\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,12.73667721,13.33616296,13.90721845,14.44873099,14.9598846,15.4404177,15.89066082\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.702681085,8.393359302,9.078721582,9.758613233,10.43059082,11.09102762,11.73599497\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.277638429,8.0346517,8.787431517,9.53141305,10.26160536,10.97321828,11.66208057\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.497461743,8.202550602,8.905045018,9.603521538,10.29458781,10.97393605,11.63716936\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,12.73929463,13.35579365,13.94260624,14.49849921,15.02262969,15.51478099,15.97537233\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,8.686425365,9.579580178,10.44208886,11.264437,12.04107666,12.76943037,13.44904284\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.410352124,8.165361207,8.916374784,9.659822887,10.3909842,11.10490075,11.79703964\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.706590158,10.42150152,11.12005479,11.79802678,12.4517581,13.07841072,13.67602556\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.81561021,10.54771241,11.25604958,11.93791196,12.59139379,13.2151945,13.80853574\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.838768808,10.56028853,11.26403372,11.94616682,12.60330901,13.23282192,13.83288606\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.574467341,8.332666873,9.085965762,9.830991002,10.56321686,11.27785298,11.9704973\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.200977768,10.09462387,10.95727555,11.77949962,12.55579738,13.28362816,13.96256875\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,13.13270378,13.74211476,14.32038712,14.86721118,15.38230328,15.86576768,16.31819362\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.975995144,8.677715338,9.371957967,10.05891838,10.73649362,11.40135186,12.04980548\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.684151089,8.448237482,9.206754565,9.9553867,10.68926235,11.40365535,12.09444605\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,7.716744515,8.433294652,9.14572282,9.852571448,10.55051793,11.23537601,11.90289437\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,12.87774435,13.5125778,14.11357506,14.68066987,15.21381477,15.7133466,16.18007707\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,15.53819969,16.18676863,16.72180894,17.17082159,17.55490344,17.89006049,18.18829681\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,15.69119664,16.31756564,16.83204287,17.26220689,17.62911711,17.94869293,18.2328383\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,15.24830925,15.91915436,16.47565788,16.9441825,17.34538279,17.69521601,18.00584986\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.599985883,10.43463851,11.24740135,12.0319206,12.78304958,13.4970933,14.17178997\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,10.23251693,10.97773591,11.69866697,12.39270701,13.0571949,13.68991719,14.28935703\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.848401611,10.72662876,11.5679397,12.36927498,13.12829077,13.84360331,14.51480381\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,10.3798536,11.13367169,11.8620802,12.56253815,13.23248588,13.86983043,14.47317771\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.905585411,10.72863608,11.53141607,12.30741725,13.05124099,13.75893657,14.42802284\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,16.69805204,17.26999699,17.74432874,18.14387844,18.48635183,18.78532247,19.05107259\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,17.32012522,17.82453319,18.24151661,18.59199847,18.89214219,19.15429509,19.38777457\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,17.06426883,17.56779803,17.99078684,18.35087416,18.66225376,18.93612852,19.18117901\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.599291795,10.43435468,11.24747862,12.03231563,12.78372471,13.49801605,14.17293237\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,10.23834277,10.98328714,11.70398301,12.39782188,13.0621375,13.69471193,14.29402445\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.848568884,10.72671442,11.56794598,12.36920349,13.12814294,13.8433806,14.51450792\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,10.38019855,11.13398779,11.86236465,12.56278961,13.23270427,13.8700166,14.47333316\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,9.905704803,10.72853322,11.53112484,12.30696981,13.0506664,13.75826021,14.42726634\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,16.70905435,17.27970252,17.7529784,18.15166146,18.49341738,18.79178893,19.05703463\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,17.31917436,17.82355723,18.24052185,18.59098922,18.89112154,19.15326527,19.38673727\n\"linker Cc1[nH][n-]c(c1Cc1cccc(n1)Cc1c(C)[n-][nH]c1C)C, [C]#N, nodes [Cu], topology pcu\",,,17.07005054,17.57270108,17.99498609,18.35450254,18.66541361,18.93889961,19.18362423\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,20.7964316,21.26414968,21.63341245,21.92946407,22.17011778,22.36817551,22.53299843\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,21.56476381,21.91957735,22.19808376,22.42033825,22.60032513,22.74799879,22.87058109\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,20.58942447,20.9685287,21.27190359,21.51793883,21.7198969,21.88749775,22.02797327\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,20.54403698,20.92941242,21.23792959,21.48821161,21.69370419,21.86426992,22.00725156\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.638664511,4.367137647,5.106517208,5.838667212,6.550575863,7.233722061,7.883205938\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.727219412,4.450166221,5.181933703,5.905537307,6.608779204,7.283659942,7.925580142\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.832605909,4.567970272,5.311010002,6.043978463,6.75434087,7.434062008,8.078691553\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.56944612,4.28717956,5.017668489,5.742900386,6.449833702,7.12981849,7.777772531\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.636997128,4.365441507,5.104778725,5.836884371,6.548754192,7.231871267,7.881337425\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.727713383,4.450270022,5.181590204,5.904726465,6.607511405,7.281967461,7.923508987\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.836002323,4.572554307,5.316624909,6.050434895,6.761444299,7.441630186,8.086563776\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,3.580536426,4.299392513,5.030681449,5.756420078,6.463609004,7.143643979,7.791486456\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.710066212,7.504869472,8.293005832,9.067992753,9.824924016,10.55987395,11.26967712\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.383909892,9.197388977,9.998809131,10.78269875,11.54350653,12.27638023,12.97755029\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.416063818,10.21399041,10.98253523,11.71893567,12.42127219,13.0883279,13.71952196\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.386004133,10.18375466,10.9542648,11.6938836,12.40007236,13.07119462,13.70639656\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.450750773,9.245648278,10.03030885,10.79943589,11.54753066,12.26968221,12.96198308\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.661780547,7.448465091,8.235768026,9.016457384,9.784138917,10.53322248,11.25901911\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.725142479,7.524886628,8.318695655,9.099627109,9.862375533,10.60271656,11.31729188\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.463999435,9.264612187,10.05403167,10.82682601,11.57750331,12.30125594,12.99432857\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.448752995,10.23947433,11.00496331,11.7409475,12.44440004,13.11333868,13.74668242\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.438686307,10.24189144,11.01717901,11.76078561,12.47010356,13.14348874,13.78013288\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.313609403,9.134016939,9.944806762,10.73878712,11.50940715,12.25128564,12.9604179\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.594025933,7.386657724,8.177265037,8.958452658,9.724220681,10.46961768,11.1906286\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.707412678,7.503198061,8.291996228,9.067413854,9.824612254,10.5597161,11.26959682\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.397386227,9.210450121,10.01130008,10.79453377,11.55464655,12.28681777,12.98729889\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.404961366,10.20248672,10.97058368,11.70654002,12.40847508,13.07519841,13.70614404\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.38342199,10.17981849,10.94884561,11.68695053,12.39167934,13.06145911,13.69547689\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.455026685,9.249842097,10.03441847,10.8034639,11.55147903,12.27355076,12.96576955\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.658177733,7.443983367,8.229788819,9.008639748,9.77436051,10.52152038,11.24553684\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.733999452,7.533764243,8.327425705,9.108062135,9.87039994,10.6102494,11.32428439\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.486206193,9.290404211,10.08289547,10.8581195,11.61056254,12.33546107,13.02913774\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.454165161,10.2467801,11.01370928,11.75071889,12.45484181,13.12416109,13.75765773\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,9.442239207,10.24751724,11.02446053,11.76932334,12.47954094,13.15352312,13.79051689\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,8.320314359,9.144035796,9.957579991,10.75372578,11.52595319,12.26894472,12.97877233\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,6.616252937,7.408377732,8.198524595,8.979252221,9.744545855,10.48945093,11.20995326\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,17.31664241,18.04310026,18.67563564,19.22599103,19.70520444,20.12321646,20.48874545\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,17.22340271,17.9500342,18.58505634,19.13923103,19.62295537,20.04575943,20.41610503\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,17.32006328,18.04605798,18.67817396,19.22816875,19.70707919,20.12483899,20.49015839\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,17.23013871,17.95754169,18.59308788,19.14756391,19.63140591,20.05418494,20.42439979\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,14.73167692,15.47793387,16.15850852,16.77875557,17.34400374,17.85929599,18.32929088\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.59461441,16.26909191,16.87142572,17.41336352,17.90391942,18.35009279,18.75740984\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,14.56611632,15.39125947,16.13025324,16.79428748,17.39254812,17.93271079,18.42130138\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.47460649,16.2044988,16.85511733,17.43882595,17.96506996,18.441267,18.87340417\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,14.51437763,15.30348635,16.01911292,16.66849543,17.25816456,17.79398602,18.28122865\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.77039419,16.4246849,17.01119304,17.5400356,18.0193238,18.45555556,18.85397253\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.6814116,16.34985497,16.94750468,17.48592312,17.97384364,18.41799566,18.82368365\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.20912744,15.96783455,16.64428846,17.25113748,17.79804081,18.29260543,18.74100586\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,14.70599306,15.45608834,16.13962743,16.76219038,17.3292727,17.84604033,18.31724207\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.53137721,16.21266527,16.82070431,17.3675005,17.86224719,18.3120721,18.72259635\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,14.59313975,15.41692674,16.15499916,16.81832453,17.41596004,17.95551211,18.44347387\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.29598918,16.04743988,16.71517233,17.31268005,17.85024258,18.33588942,18.77605439\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,14.79722759,15.55686264,16.24731476,16.87500092,17.44582405,17.96516373,18.4379068\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.68076416,16.34242683,16.935602,17.47044772,17.95512459,18.3961876,18.79893822\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.73628474,16.40286217,16.99854744,17.5348816,18.02062611,18.46255445,18.86601478\n\"linker [O-]C(=O)c1ccc(s1)C(=O)[O-], nodes [Ca], [Cu], topology \",,,15.46063431,16.19079776,16.84350542,17.43034176,17.96018121,18.44004647,18.87567125\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,18.54517596,18.72660289,18.86980897,18.98470958,19.07822786,19.15530845,19.2195549\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,18.39490878,18.58068436,18.72731363,18.84494986,18.94068382,19.01958074,19.08533244\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,12.59475044,12.78079822,12.92801753,13.04634828,13.14278795,13.22236146,13.28874441\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,20.89093221,21.22687695,21.49748587,21.71810625,21.89998139,22.05145161,22.17878234\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,20.88547654,21.2637239,21.56919382,21.81871638,22.02471728,22.19646957,22.340972\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.58907563,12.5700671,13.48733384,14.3375838,15.12017418,15.83662848,16.49000705\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.45721152,12.41076295,13.30825278,14.14418413,14.91629911,15.62496947,16.27244874\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.25640897,12.20464381,13.09199058,13.91659209,14.67830378,15.37854363,16.01993462\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.78253855,12.69404388,13.54999892,14.34787955,15.08702328,15.76836716,16.39406611\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.65019088,12.62646447,13.53937667,14.3857679,15.1650489,15.87873573,16.52984488\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.29265313,12.23783165,13.12877183,13.95967985,14.72801605,15.43390232,16.07938031\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.5046587,12.48045017,13.39089243,14.233551,15.00844628,15.71754129,16.3641485\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,11.78559227,12.71833302,13.59205151,14.40406872,15.15391518,15.84290769,16.47365531\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,3.64528515,4.214513346,4.809237986,5.417342992,6.027908206,6.632048091,7.223139715\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,4.103729229,4.729574202,5.370222314,6.012656485,6.646312109,7.263393792,7.858706081\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,3.745775745,4.336937232,4.949974267,5.572148844,6.192474192,6.802338285,7.395567156\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,4.071027391,4.685563867,5.31639889,5.950660084,6.57772235,7.189610619,7.780897677\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,3.817048628,4.387716772,4.982167056,5.588433395,6.195810026,6.79564301,7.381531551\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,4.179113242,4.795472739,5.426863746,6.060653901,6.686484581,7.296628756,7.88586905\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,3.922985496,4.517144959,5.131782061,5.754191945,6.373489344,6.981198594,7.571294205\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,3.854202258,4.433525633,5.035939574,5.649048677,6.261982842,6.866109405,7.455159087\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,9.958773757,10.96869635,11.92131319,12.80868589,13.62805493,14.3801366,15.06781352\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,9.722932426,10.72456205,11.67259729,12.55812945,13.37758099,14.13102922,14.82088068\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,10.16070618,11.1796974,12.13693616,13.02523237,13.84266226,14.59070695,15.27288657\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,10.07334958,11.07720873,12.02395399,12.90565144,13.71954338,14.46635314,15.14897317\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.33217249,15.26182866,16.08900931,16.8258296,17.4826834,18.06870512,18.59201915\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.31535405,16.13849821,16.87445853,17.53335486,18.12348452,18.65210309,19.12575487\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.62673492,15.55638574,16.37960471,17.11120547,17.76298429,18.34472142,18.86476634\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,12.84359971,13.65623678,14.38568892,15.03963321,15.62521376,16.14921078,16.61802977\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.83261472,15.75474951,16.57366378,17.30168287,17.9493534,18.52596462,19.03979579\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,12.99401861,13.84757242,14.60867683,15.2890409,15.89811613,16.44390883,16.93341954\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.12336497,16.02021479,16.81802935,17.52782289,18.15935306,18.72143667,19.22206343\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.0211854,15.91659867,16.7124474,17.41953851,18.04766181,18.60577273,19.10202916\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.94923602,15.90575694,16.75163561,17.49903666,18.15929703,18.74285317,19.25916705\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.27969234,15.95460693,16.57380439,17.14441094,17.67096522,18.15671539,18.60434435\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.5570476,15.3636933,16.09083128,16.74856956,17.34459756,17.8851551,18.37559823\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.54773495,15.42792473,16.21640838,16.92406422,17.55991235,18.13169513,18.64623126\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.3426632,15.25276363,16.06220175,16.781745,17.42125371,17.98977354,18.49554799\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.27025186,16.04228232,16.7367956,17.36303496,17.92808623,18.43792545,18.89789794\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.72927085,15.65315877,16.47099188,17.19738691,17.84405636,18.4207642,18.93587753\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.52407613,16.35682873,17.10162721,17.76739951,18.36217533,18.89337558,19.36787679\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.94792289,15.83357098,16.62299578,17.32788931,17.95790772,18.52139906,19.02576372\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.94488868,15.86741819,16.68406781,17.40743725,18.04860365,18.61741374,19.12263576\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.4019096,16.26440108,17.03348815,17.71913302,18.33025062,18.87498243,19.36077614\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.27987472,15.23221461,16.08041594,16.83528487,17.50683181,18.10431833,18.63623548\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.86906182,15.82409171,16.66990483,17.41833869,18.08042105,18.66632831,19.18531796\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,15.21144312,15.92074618,16.57021283,17.16652772,17.71422533,18.21684935,18.67754494\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.38135675,15.13130188,15.81116873,16.42874792,16.99006099,17.50016414,17.96357308\n\"linker [O]P(=O)(CP(=O)([O])[O])[O], nodes [U], [Zn], topology pcu\",,,14.66052526,15.54484237,16.33420551,17.04056284,17.67363726,18.24165942,18.75179975\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,21.96134473,22.32108621,22.60484784,22.83222185,23.0169796,23.16899444,23.29547509\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,21.6528089,22.03712291,22.3459152,22.59709376,22.80372618,22.97547985,23.1196013\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,22.20970848,22.53577751,22.79160165,22.99573803,23.16107117,23.29674958,23.40940112\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,22.26424327,22.58143787,22.83031205,23.02892634,23.18981275,23.32186571,23.43152747\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,21.60503327,21.99231751,22.3045701,22.55925816,22.76923668,22.94408067,23.09100693\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,21.96141117,22.32114245,22.60489595,22.83226342,23.01701584,23.16902628,23.29550328\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,21.65271172,22.03703546,22.34583651,22.5970229,22.80366225,22.97542205,23.1195489\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,22.20978328,22.5358397,22.79165411,22.99578284,23.16110988,23.29678333,23.4094308\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,22.2644383,22.58160374,22.83045454,23.02904986,23.18992073,23.32196083,23.43161183\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,21.60494058,21.9922353,22.30449704,22.55919304,22.76917842,22.94402836,23.09095977\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.350781832,4.006870791,4.684109808,5.365895124,6.039265795,6.694856659,7.326467053\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.441442321,4.090599176,4.763490704,5.442700594,6.114579475,6.7692536,7.400185062\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.427615999,4.093909736,4.783762429,5.478890274,6.165060261,6.832094723,7.473375569\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.457580771,4.118373051,4.802219149,5.491386647,6.172000098,6.83408275,7.471103314\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.062468839,3.701422746,4.371990587,5.055282242,5.73613786,6.403345981,7.049275643\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.677896535,4.347703458,5.031014007,5.712764434,6.381494151,7.029149907,7.650606898\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.454182806,4.118414612,4.806527678,5.500280628,6.18538969,6.851600809,7.492224248\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,2.998046538,3.633242286,4.302586021,4.986653828,5.669720943,6.34007665,6.989691963\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.528521771,4.19014895,4.868054104,5.546877391,6.214797557,6.863386634,7.487163357\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.320674988,3.980402141,4.661012354,5.345810303,6.021811801,6.679667942,7.313213542\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.388482445,4.042630016,4.720356891,5.404136698,6.080267644,6.738867143,7.373416705\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.461255174,4.125423506,4.810972734,5.500578318,6.180761778,6.841874766,7.477632906\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,4.070124806,4.98288956,5.880158213,6.738567204,7.544480492,8.291367095,8.977494261\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,4.786308697,5.748980545,6.671397862,7.535387388,8.332371204,9.060143628,9.720410527\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.350833572,4.00692522,4.68416528,5.365950402,6.039320002,6.694909207,7.326517571\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.441483019,4.090643039,4.763536634,5.442747605,6.114626748,6.769300483,7.400231054\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.4275875,4.093876589,4.783725376,5.478850188,6.165018017,6.832051125,7.47333132\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.457589491,4.118382067,4.802228291,5.491395775,6.172009101,6.834091548,7.471111851\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.062465626,3.701420155,4.371988831,5.055281424,5.736137995,6.403347023,7.049277511\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.677886362,4.347692231,5.031002275,5.71275261,6.38148253,7.029138687,7.650596205\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.454184201,4.118411739,4.806521207,5.500271241,6.185378023,6.851587425,7.492209628\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,2.998022928,3.633213155,4.302552453,4.986616884,5.669681595,6.340035742,6.989650208\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.528630607,4.190255192,4.86815632,5.546974737,6.214889612,6.863473267,7.487244631\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.320656255,3.980384573,4.660996025,5.345795245,6.021798006,6.679655367,7.313202122\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.388470376,4.042619936,4.720348632,5.404130055,6.080262405,6.738863107,7.373413685\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,3.461276849,4.125446411,4.810996114,5.500601615,6.180784601,6.841896856,7.477654103\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,4.070081594,4.982851607,5.88012482,6.738537737,7.544454402,8.291343911,8.977473587\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,4.786401932,5.749087282,6.671512803,7.535506365,8.332491113,9.060262257,9.720526364\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.655427616,10.39259312,11.11125154,11.80796024,12.47949621,13.12320673,13.73716876\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,10.00011662,10.73815953,11.44899803,12.1309961,12.78310057,13.4046482,13.99531374\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.851790926,10.60403338,11.3304665,12.02892994,12.69766181,13.3353547,13.94120101\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.935970361,8.720936877,9.495256121,10.25523384,10.99665835,11.71543989,12.40804216\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.803208071,7.606272326,8.398762623,9.175603332,9.932889011,10.66739389,11.3764287\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.118477504,7.979172019,8.839867768,9.689025622,10.51716013,11.31694926,12.08312723\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.267160507,8.074289021,8.866130722,9.638008463,10.38656372,11.10922886,11.80401291\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.952723044,7.807924813,8.662118338,9.504927316,10.3276367,11.123353,11.88697952\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.12970471,7.922266514,8.700859211,9.461547449,10.2014415,10.91812755,11.60951714\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.985964958,7.763550593,8.535944164,9.297396393,10.04315511,10.76914587,11.47192224\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.909598625,8.70147876,9.482774129,10.24945583,10.99707478,11.72139872,12.41882685\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.832024508,10.59249449,11.32761313,12.03472476,12.71166157,13.35683636,13.96928069\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.948566047,10.70866199,11.4368197,12.13264078,12.79587753,13.42640483,14.02427798\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.601793077,10.34894424,11.07776115,11.78420926,12.46470668,13.11641676,13.73735317\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.160546622,7.965141697,8.753333451,9.521614563,10.26740858,10.98854842,11.68315366\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.005296814,7.858625339,8.70987432,9.549093422,10.36790592,11.15966585,11.91944485\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.923694616,7.720015848,8.503931241,9.271019603,10.01796123,10.74201269,11.44085277\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.945745178,8.725611,9.495434871,10.25153736,10.9896818,11.70573561,12.39611108\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.846613197,10.60130668,11.32988403,12.03034585,12.70095645,13.34038814,13.94780567\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.933494146,10.68294509,11.40174993,12.08963823,12.7463684,13.37174219,13.96569502\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.604980351,10.34982484,11.07564466,11.7787772,12.45592913,13.10446248,13.7225131\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.664833495,10.4093678,11.13366555,11.83459542,12.50920318,13.15506148,13.77043336\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,10.01563068,10.76684116,11.48755789,12.17683854,12.83417771,13.45934423,14.05235523\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.840150112,10.60534818,11.34211445,12.04878427,12.72396784,13.36665302,13.97627614\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.815332772,8.621797199,9.416076102,10.19401097,10.95122612,11.6836515,12.38787661\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.90762154,7.703773305,8.491575476,9.265626823,10.0215617,10.75568424,11.46489516\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.144066259,8.005120419,8.865725511,9.71440666,10.54178476,11.34063893,12.1057839\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.280688459,8.084471494,8.874463867,9.645540375,10.39397046,11.11690602,11.81215866\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.655451209,10.39262286,11.11128627,11.80799888,12.47953779,13.12325042,13.73721386\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,10.0001412,10.73818833,11.44902978,12.1310297,12.78313515,13.40468312,13.99534851\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.851797827,10.60404368,11.33047884,12.02894335,12.69767559,13.33536841,13.94121435\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.935985657,8.72095218,9.49527101,10.25524799,10.99667152,11.71545199,12.40805313\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.803299599,7.606381731,8.398882111,9.175727221,9.933013298,10.66751586,11.37654657\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.118719857,7.979417906,8.840110428,9.689260552,10.51738459,11.31716178,12.08332723\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.267306845,8.07445193,8.866302935,9.638184782,10.38674049,11.10940354,11.80418378\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.952737062,7.807936716,8.662128631,9.504936368,10.32764477,11.12336029,11.88698618\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.129665303,7.922232946,8.700830276,9.46152226,10.20141939,10.91810798,11.60949971\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.985980448,7.763559129,8.535947618,9.29739611,10.04315207,10.76914081,11.4719157\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.909604147,8.701481269,9.482774447,10.24945457,10.99707241,11.72139558,12.4188232\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.832019403,10.59249145,11.32761187,12.03472505,12.71166321,13.35683916,13.96928448\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.948565065,10.70866272,11.43682193,12.13264433,12.79588224,13.42641053,14.02428453\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.601808021,10.34895823,11.07777436,11.78422186,12.4647188,13.11642851,13.73736461\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.160582505,7.965168981,8.753354076,9.521629974,10.26741987,10.98855643,11.68315904\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.005313334,7.858640601,8.709888273,9.549106048,10.36791724,11.15967589,11.91945369\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.923720146,7.720035191,8.503946089,9.271031176,10.01797041,10.74202014,11.44085895\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.945721129,8.725583609,9.495405631,10.25150727,10.98965156,11.70570567,12.39608176\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.846671916,10.60135748,11.3299287,12.03038565,12.70099228,13.34042067,13.94783539\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.933591778,10.68303437,11.40183097,12.08971138,12.74643417,13.37180113,13.96574774\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.605010285,10.34985144,11.07566805,11.77879768,12.45594703,13.10447812,13.72252678\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.664816768,10.40935169,11.13364955,11.8345793,12.50918685,13.15504497,13.77041672\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,10.01563545,10.76684484,11.48756058,12.17684035,12.83417875,13.45934463,14.05235508\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,9.840133152,10.60533186,11.34209862,12.04876883,12.72395275,13.36663827,13.97626173\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.815277649,8.621749389,9.416033901,10.1939731,10.95119167,11.68361979,12.38784714\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,6.907542541,7.70370133,8.491508399,9.265563242,10.02150074,10.7556254,11.46483816\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.144038549,8.005095708,8.865703215,9.714386349,10.54176611,11.34062172,12.10576794\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,7.280672007,8.08445,8.874438183,9.645511266,10.39393863,11.11687211,11.81212325\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.524716134,9.365577354,10.18251297,10.97367442,11.73646083,12.46816877,13.16648587\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.57641623,9.429846209,10.25741946,11.05717566,11.82655755,12.56301302,13.26444293\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.54584175,9.400692283,10.22847184,11.02764226,11.79601306,12.53131057,13.23162562\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.536312002,9.381149276,10.20159052,10.99570517,11.7608676,12.49439296,13.19401562\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.52482884,9.365700537,10.18264199,10.97380583,11.73659217,12.4682983,13.16661241\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.576350213,9.429783625,10.25736108,11.05712174,11.82650808,12.56296781,13.2644017\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.545977062,9.400822487,10.22859535,11.02775838,11.79612163,12.53141175,13.23171974\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,8.536281042,9.381123473,10.20156858,10.99568615,11.76085084,12.49437797,13.19400204\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.36613674,16.25521406,17.03613138,17.72462817,18.3338015,18.87455868,19.35603529\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.10496633,15.91763274,16.63663458,17.27749723,17.85198717,18.36924379,18.83655797\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,16.24155283,16.859726,17.40798317,17.89953793,18.34416565,18.74918518,19.12014873\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.16505208,15.90572731,16.56876238,17.16553139,17.70517555,18.1950692,18.64121766\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.65893988,15.47106936,16.19697319,16.8485298,17.43559132,17.96631198,18.44747527\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.23602207,16.15432059,16.9603379,17.6701302,18.29713727,18.8526413,19.34616694\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.05154222,15.83448285,16.53057303,17.15317558,17.71295088,18.21844361,18.67657302\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,16.30295597,16.93300826,17.49605047,18.0034292,18.4636179,18.88307034,19.26681382\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.95967298,16.61297789,17.19878215,17.72759937,18.20759973,18.64519545,19.04549207\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.65217465,15.47517981,16.21670965,16.88539954,17.48914618,18.03501767,18.52927801\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.44780705,16.33881151,17.12194433,17.8124762,18.42319445,18.96485034,19.44653964\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.9349295,16.61035745,17.21122276,17.75040264,18.23754762,18.68002271,19.08356661\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.39658859,16.14990884,16.8186323,17.41653293,17.95426255,18.44016756,18.88090088\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.86847221,15.65070843,16.34662727,16.96988106,17.53120398,18.03910222,18.50039929\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.26020901,15.99822664,16.66043744,17.2571175,17.79679668,18.28652655,18.73216308\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.22737795,16.14352414,16.94594632,17.6515708,18.27443311,18.82617292,19.31649548\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.69706886,15.52652641,16.27194722,16.94278815,17.54748458,18.09346276,18.58723048\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.44960669,16.17185189,16.81382567,17.38877643,17.90698815,18.37651089,18.80372082\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,16.12097848,16.75410137,17.31383495,17.8144518,18.26642192,18.67753256,19.05365834\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.84338651,16.57799693,17.22903676,17.81098195,18.33438021,18.80720873,19.23573378\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,17.29754085,18.22683503,18.99345763,19.63059817,20.16419246,20.61444516,20.99713214\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,17.54140854,18.4452766,19.18957506,19.80724335,20.32386977,20.75931279,21.12903698\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.36580534,16.25493577,17.03589599,17.7244276,18.33362933,18.87440984,19.35590574\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.10539868,15.91803584,16.63701055,17.27784834,17.85231559,18.36955147,18.83684667\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,16.24003344,16.85840745,17.40682647,17.89851336,18.34325033,18.74836128,19.11940221\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.16365388,15.90450614,16.56768323,17.16456788,17.70430754,18.19428117,18.6404975\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.65923576,15.4713411,16.19722562,16.84876633,17.43581439,17.96652333,18.44767619\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.23687126,16.15505732,16.96098124,17.67069566,18.29763737,18.85308623,19.34656496\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.05117443,15.83415315,16.5302758,17.15290626,17.71270572,18.21821954,18.67636747\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,16.30286314,16.93293387,17.49599025,18.00338005,18.46357754,18.88303701,19.2667862\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.96065458,16.61381546,17.19950454,17.72822827,18.20815179,18.64568364,19.04592662\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.65209737,15.47511764,16.21665938,16.8853587,17.48911288,18.03499042,18.52925565\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.44615062,16.33738707,17.12070919,17.81139681,18.42224431,18.96400836,19.44578892\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.93444866,16.60992491,17.2108319,17.75004755,18.2372233,18.67972499,19.08329207\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.39819469,16.15134268,16.81991679,17.41768822,17.95530595,18.44111379,18.88176238\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.86917136,15.65131219,16.3471546,16.97034631,17.53161816,18.03947385,18.50073504\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.26003822,15.99808016,16.66030962,17.25700429,17.7966951,18.28643442,18.73207876\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.22731114,16.14346905,16.94590055,17.65153245,18.27440069,18.82614525,19.31647168\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,14.69649969,15.52601759,16.27148971,16.94237456,17.54710885,18.09311989,18.58691633\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.44916108,16.17145776,16.81347597,17.38846503,17.90670982,18.37626118,18.80349596\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,16.12114086,16.75423879,17.31395233,17.81455286,18.26650959,18.6776091,19.0537256\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,15.84340617,16.57801607,17.22905546,17.81100005,18.33439753,18.8072251,19.23574911\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,17.29654236,18.22593827,18.99265334,19.62987629,20.16354327,20.61385977,20.99660267\n\"linker [O-]C(=O)c1[n+]([O-])cccc1C(=O)[O-], nodes [Mn][OH]([Mn][OH]([Mn])[Mn])[Mn], topology pcu\",,,17.54041322,18.44439737,19.18879683,19.80655227,20.32325368,20.75876125,21.12854113\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,4.178840773,5.459264452,6.752466632,8.016277999,9.22336603,10.35797074,11.41264642\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,4.070342614,5.335030534,6.617071508,7.873883463,9.07745899,10.2113112,11.26732381\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,4.085257243,5.351505892,6.634515187,7.891797825,9.095454673,10.22909949,11.28470065\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,4.110255646,5.380333176,6.666124993,7.925214171,9.12984452,10.26379316,11.3191839\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,4.039499792,5.300136261,6.579544244,7.834927626,9.038025691,10.17211269,11.22886979\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,4.169962212,5.446008576,6.73524086,7.995729866,9.200220458,10.33292887,11.38633288\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,21.71290774,21.89183209,22.03063076,22.14036401,22.22855666,22.30046309,22.3598373\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.610704018,4.279641532,4.962436915,5.644134279,6.313273877,6.961739102,7.584311739\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.650326648,4.311768456,4.991545456,5.673248772,6.344212987,6.995440953,7.621131931\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,2.976562834,3.618462319,4.291787829,4.977935724,5.66183008,6.332240069,6.981472832\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.023456329,3.657672915,4.320918836,4.995792808,5.668168417,6.327465471,6.966376197\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.462115176,4.123006976,4.806884857,5.49596997,6.176380165,6.838155412,7.474790591\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.70704718,4.383712543,5.070733019,5.753879411,6.422383608,7.068718308,7.688136443\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.616388944,4.285670177,4.968742114,5.650626747,6.319861031,6.968335573,7.590844137\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.601046377,4.256477379,4.931523432,5.609792942,6.278549202,6.928675538,7.554231712\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.037963392,3.681926636,4.355943515,5.041671284,5.724307653,6.392868639,7.039865544\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.067099728,3.70661834,4.37352443,5.050607559,5.723993466,6.383358134,7.021624818\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.487397534,4.147629046,4.830451289,5.518238449,6.197228428,6.85754853,7.49275305\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.716018092,4.391925166,5.078190374,5.760634634,6.428508582,7.074287249,7.693218242\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.592517964,4.26090532,4.94335251,5.624875712,6.293993222,6.942568887,7.565365781\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.656017231,4.320687134,5.003810251,5.688666463,6.362404337,7.015938502,7.643447703\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.059620406,3.707514488,4.385152456,5.073983508,5.759105733,6.429515908,7.077758626\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.004031645,3.639430176,4.304188646,4.980733509,5.654808491,6.31574527,6.956182505\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.47308134,4.134718697,4.81906347,5.508360043,6.188767181,6.850371054,7.486710442\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.698131707,4.376337936,5.06484227,5.749337056,6.419017692,7.066348601,7.686591192\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.610216771,4.277660161,4.959175951,5.639827873,6.308149074,6.956001241,7.57813813\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.66026954,4.320514103,4.999191154,5.67990563,6.349994355,7.000455337,7.625479184\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,2.991221163,3.630800529,4.301787686,4.985721439,5.667607896,6.336253696,6.983973535\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,2.978982461,3.611482997,4.27341339,4.947417249,5.619370898,6.278665484,6.917945145\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.482985271,4.143228824,4.825974467,5.513649017,6.192526369,6.852754974,7.48789926\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,3.714048498,4.391110994,5.078347162,5.761554122,6.429998023,7.076184179,7.695392888\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.538059746,10.30780759,11.0506559,11.76453642,12.44776849,13.09909763,13.71774619\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.814666288,10.57478362,11.3077117,12.01103285,12.68302109,13.32257921,13.92917969\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.068738984,8.925442821,9.759933454,10.56820591,11.34675519,12.09269846,12.80389221\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.426795323,10.24673777,11.03277955,11.78283636,12.49556432,13.1703239,13.80710278\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.238801895,8.080153296,8.907183041,9.715277163,10.50014517,11.25797733,11.98564151\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.312112973,8.149916352,8.971931554,9.774116896,10.55266077,11.30411973,12.02562001\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.383217692,10.19484,10.97415912,11.71888112,12.42748964,13.09919621,13.73385291\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.074931941,8.935208847,9.773032541,10.58421963,11.3652091,12.11312274,12.82585065\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.843493798,10.6113436,11.35040176,12.05876766,12.73497979,13.37806537,13.98755641\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.517786051,10.30091539,11.05690036,11.78322752,12.47787801,13.13937869,13.76684435\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.574408215,10.34163038,11.08204637,11.79360985,12.47465514,13.12393691,13.74068158\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.861220746,10.61866507,11.34893658,12.04965033,12.71910636,13.3562285,13.96050593\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.07084105,8.927426765,9.762261497,10.57113685,11.35040953,12.0971037,12.80901578\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.463450131,10.28308745,11.06926646,11.8196473,12.53270673,13.20769307,13.844534\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.262982892,8.107961603,8.938278784,9.749253856,10.53654079,11.29630352,12.02541389\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.316121563,8.158313367,8.984203077,9.789745344,10.57112415,11.32490661,12.0482467\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.37213218,10.18929843,10.97324047,11.72178353,12.4335106,13.10772378,13.74435947\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.073077845,8.934633594,9.773044574,10.58443467,11.36542059,12.11322683,12.82580235\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.855935239,10.62074803,11.35699282,12.06280158,12.73672612,13.3777958,13.9855364\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.525609169,10.30676434,11.06049531,11.78451649,12.47695701,13.13643333,13.76210756\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.526226712,10.29723031,11.04116704,11.75598014,12.44001074,13.09202683,13.71127061\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.839610504,10.59635991,11.32650973,12.02750585,12.6975273,13.3354087,13.94057189\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.065607274,8.920851651,9.754979416,10.56352004,11.34267068,12.08936318,12.8013425\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.461769686,10.27680598,11.05962205,11.80759674,12.51899248,13.19289168,13.82909195\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.236247367,8.082220613,8.913500639,9.725319568,10.51332389,11.27370296,12.00336194\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.286385813,8.129523621,8.956691948,9.763637409,10.54642995,11.30157909,12.02621312\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.384731885,10.19758969,10.97797591,11.72361115,12.43298641,13.10532087,13.74047656\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.054573072,8.917788897,9.758273059,10.57181527,11.35484597,12.10449925,12.81869148\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.847786767,10.61542516,11.35417903,12.0621771,12.73798089,13.38063825,13.989699\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.516813651,10.30060446,11.05707984,11.78375646,12.47864213,13.14028838,13.7678319\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.553861703,10.32080374,11.06097297,11.77237838,12.45337934,13.10273633,13.71966991\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.855812614,10.61137788,11.34020226,12.03981229,12.70844681,13.34498372,13.94887432\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.091319853,8.943842287,9.774629372,10.57971694,11.35558751,12.09931508,12.80869913\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.456959551,10.27556766,11.06073681,11.81022678,12.52256224,13.19700557,13.83347811\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.284849287,8.129768263,8.959997058,9.770852167,10.55797702,11.31752565,12.04636427\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,7.307942032,8.149370512,8.975129676,9.780983372,10.56296119,11.31751097,12.04169866\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.363555974,10.18305733,10.96880951,11.71875131,12.43155748,13.10660095,13.74387222\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.088897044,8.950565343,9.788776552,10.59973073,11.38011658,12.12721945,12.83903618\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.842214623,10.61047656,11.34979717,12.0582697,12.73445472,13.37741278,13.98670999\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,9.537870028,10.31866352,11.07262567,11.79716934,12.49023072,13.15030899,13.77650064\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.58559683,12.45368532,13.2730229,14.04307902,14.763515,15.43459884,16.05733115\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.71269654,12.54587408,13.33610925,14.08204958,14.78268765,15.43769806,16.0475392\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.64556465,12.50592175,13.31995751,14.0863055,14.80405283,15.4730829,16.09414604\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.65739235,12.50531378,13.30587311,14.05895887,14.76449704,15.4228461,16.03495467\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.50254025,12.34004893,13.13535564,13.88700032,14.5938714,15.25552658,15.87229982\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.60338783,12.45116662,13.25251768,14.00700983,14.71434242,15.37471509,15.98896554\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.55200989,12.41658901,13.23353719,14.00213783,14.72188234,15.39288413,16.01600716\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,11.92930329,12.78250382,13.58586695,14.33936531,15.04311057,15.69773393,16.30450567\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.226319181,9.054496207,9.862704933,10.64874284,11.40955231,12.14195143,12.84316405\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.325410644,9.157951349,9.969983039,10.75904248,11.52196183,12.25554826,12.95707839\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.235509273,9.065726835,9.875291375,10.66217931,11.4234661,12.15606851,12.85728361\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.318800919,9.153412486,9.966936563,10.75712452,11.52092684,12.25521831,12.95731666\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.220066058,9.054432437,9.867981669,10.65851909,11.42302759,12.15838999,12.86190944\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.29794504,9.134971346,9.950584906,10.74260352,11.50801399,12.24371677,12.94705153\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.221711853,9.052451747,9.862707147,10.65038269,11.41249634,12.14592386,12.84793553\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,8.286578179,9.120217104,9.933442952,10.72376984,11.48800589,12.22293684,12.92582093\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,22.76584522,23.038487,23.25036922,23.41813723,23.55315402,23.66337155,23.75448037\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.81705565,15.76206395,16.58829528,17.3142684,17.95505513,18.52296351,19.02812487\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,15.61122361,16.44752962,17.18274431,17.83253013,18.40939748,18.92347864,19.38310469\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.17786735,15.07288861,15.87169142,16.58840526,17.23374709,17.81619118,18.34272796\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.5822781,15.4855614,16.29138351,17.01221826,17.65816566,18.23773502,18.75830582\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.74893671,15.56628119,16.30078897,16.96403438,17.56464874,18.10943857,18.60407042\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.73369028,15.61879247,16.41168976,17.12288424,17.76122671,18.33446125,18.84951058\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.99394753,15.77638786,16.48165641,17.12022601,17.69992301,18.22693376,18.70642613\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,15.05241122,15.82038188,16.51208357,17.13863967,17.70810946,18.22666591,18.69933389\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,21.64871654,22.13714395,22.51991841,22.82488815,23.07146648,23.27346181,23.44088248\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.72772469,15.67877253,16.51060443,17.24177809,17.8873931,18.45978036,18.96909204\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,15.27920834,16.16121551,16.93414459,17.61523966,18.21826775,18.75435217,19.23260532\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,15.95653392,16.6354458,17.25311554,17.81711523,18.33282854,18.80447198,19.23565747\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.49395775,15.39916621,16.20686302,16.92967785,17.57779926,18.1597591,18.68291517\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.3390632,15.21474676,15.99994704,16.70672583,17.3444374,17.92068564,18.44192042\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.55414964,15.46021612,16.27114483,16.99789204,17.64967831,18.23455739,18.75971503\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.84738664,15.64211372,16.35650632,17.00225352,17.58795217,18.12025738,18.60461034\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.55978822,15.38803668,16.12948222,16.7974581,17.40176817,17.94993216,18.44800666\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,22.81264911,23.12105023,23.361129,23.55145681,23.70476312,23.82998673,23.93354237\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.58533192,15.5508721,16.39654666,17.14045457,17.79752005,18.38005849,18.89829107\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.64397641,15.60354571,16.44271825,17.1802349,17.83135992,18.40856316,18.92211037\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.72553502,15.56735867,16.32294039,17.00351818,17.61784235,18.17307722,18.67534544\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.30730362,15.15283722,15.91012162,16.59227265,17.20923698,17.76877521,18.2771758\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,15.21778636,16.00385113,16.71496189,17.35928854,17.94338125,18.47286096,18.95277724\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.17899401,15.12467763,15.97047952,16.72770888,17.40608226,18.01416525,18.5596176\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.95539761,15.73601354,16.43906955,17.07553555,17.65350587,18.1792815,18.65804992\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.53323874,15.3618631,16.10429782,16.77360017,17.37938679,17.92905974,18.4286062\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,21.86463378,22.32442168,22.6832216,22.96813009,23.19786755,23.38565477,23.54101901\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.60632284,15.57087596,16.41420263,17.15517892,17.80919568,18.38882986,18.90443433\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,15.46216913,16.3231119,17.07732826,17.74199851,18.33070912,18.85435791,19.32182488\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.81412131,15.63149485,16.3639598,17.02405982,17.62102081,18.16200558,18.6528875\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.58499902,15.48540157,16.28887195,17.00780641,17.65224852,18.23065674,18.75036137\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.41170338,15.26887361,16.03808301,16.73133675,17.35782024,17.92490232,18.43876955\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.23773716,15.1890525,16.03789682,16.79639192,17.47479205,18.08203194,18.626034\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,14.29818474,15.16628049,15.94279386,16.6411471,17.27146579,17.84170652,18.35840268\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,15.44870233,16.18661895,16.85131677,17.45375332,18.00162392,18.50072163,18.95574173\n\"linker [O]S(c1cc[n+](c(c1)c1cc(cc[n+]1[O-])S([O])([O])[O])[O-])([O])[O], nodes [Eu], [Na]O[Na], [Na]O[Na]O[Na], [O][Na], topology rna\",,,20.95820063,21.53304457,21.98959237,22.35720532,22.65696731,22.90423254,23.11034314\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,18.80688245,19.21653597,19.53909224,19.79728092,20.00698752,20.17953912,20.32316641\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,18.78777479,19.20038704,19.5252849,19.7853529,19.99658754,20.17039644,20.31506953\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,4.677687973,5.369009267,6.024201935,6.643573486,7.228661597,7.781375626,8.303670835\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,4.547351576,5.249020354,5.915738341,6.546660526,7.14258008,7.704925503,8.235328854\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,5.773137608,6.439178737,7.056459834,7.631134301,8.168224202,8.671555911,9.143995056\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,5.048515428,5.736188798,6.38130277,6.986412636,7.554530723,8.088415317,8.590396109\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,4.686568523,5.377692816,6.032526916,6.651456614,7.236069468,7.788305788,8.310139585\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,4.55043503,5.251817722,5.918236154,6.548865522,7.144509664,7.706602224,8.236777177\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,5.803444392,6.468538418,7.084410712,7.65746721,8.192880343,8.694562795,9.165427176\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,5.077278428,5.764985007,6.409563302,7.013798638,7.58085365,8.113582797,8.614376415\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,6.972099521,7.687202901,8.391987415,9.084859679,9.764139609,10.42784181,11.07378845\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,6.994876918,7.69728301,8.392127525,9.07806494,9.753218431,10.41516905,11.06122166\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,6.970612026,7.685647044,8.39042917,9.083338918,9.762678837,10.42645237,11.07247472\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,6.995995685,7.69884391,8.393869285,9.079829671,9.75491402,10.41674512,11.06265409\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.79470966,10.55560034,11.31149178,12.05362903,12.77376859,13.46527864,14.1234569\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.19735211,10.91694615,11.63310872,12.33774927,13.02326782,13.6834356,14.31368944\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,14.36010377,14.95837249,15.50315525,16.00068839,16.45632507,16.87464764,17.259571\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.904824221,10.67116719,11.43118049,12.1758144,12.89683139,13.58777577,14.2441959\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.31354619,11.04990934,11.77982499,12.49495781,13.18781546,13.85248287,14.48480572\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.39550068,11.11762924,11.83638599,12.54262268,13.22826523,13.88699099,14.51436003\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.26431299,10.98506351,11.7034549,12.41030248,13.09745593,13.75847808,14.38879239\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.808339533,10.58346887,11.35278366,12.10652413,12.83605486,13.53472822,14.19803\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.868830311,10.62467999,11.37713477,12.11641273,12.833764,13.52236129,14.17747279\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,14.38958004,15.01001895,15.57609287,16.09300138,16.56559301,16.99827492,17.39498485\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.845196313,10.60079374,11.35216814,12.0904115,12.80716657,13.49571494,14.15128677\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.19650637,10.91565729,11.6315048,12.33593053,13.02131241,13.68140367,14.31162651\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,14.36092855,14.95901853,15.50359718,16.00092199,16.45635891,16.87449765,17.25925682\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.888387918,10.65723951,11.41926334,12.16552999,12.88788825,13.57994561,14.23729746\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.28656115,11.02437864,11.75561034,12.47197483,13.16600665,13.83180215,14.46521023\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.39222652,11.11427399,11.83292004,12.5390534,13.22461872,13.88330058,14.51065949\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,10.26079031,10.98236892,11.70136131,12.40865814,13.0961554,13.75744552,14.38797158\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.797878813,10.57433318,11.34473047,12.09936684,12.8296482,13.52895761,14.19280383\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,9.836309703,10.59780889,11.35487286,12.09792291,12.81836858,13.50950983,14.16671729\n\"linker NC1=NN=N[N]1, nodes [Zn], topology dia\",,,14.29391652,14.92687315,15.50300667,16.02814021,16.50755982,16.94598578,17.34758435\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,20.46925426,20.94743193,21.32989859,21.64003469,21.89461578,22.10590205,22.28300299\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,20.50012086,20.97365978,21.35242695,21.65957327,21.91170838,22.12097105,22.2963807\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,20.5035134,20.97661636,21.35501828,21.66185774,21.91373385,22.1227767,22.2979987\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,20.47198934,20.94975205,21.33188603,21.64175294,21.89611405,22.10721879,22.28416848\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,20.72790886,21.14724948,21.48776916,21.76728288,21.99901149,22.19289641,22.35650162\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,20.77875711,21.19093482,21.52561592,21.80032882,22.02807548,22.21862965,22.37942631\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.289434516,3.935128751,4.604569439,5.280984065,5.951095754,6.605187736,7.236729418\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.403282389,4.053745831,4.728926855,5.411289363,6.086886797,6.745530346,7.380421201\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.344022501,4.016745575,4.711369346,5.410130186,6.099176802,6.768601444,7.411969524\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.320983617,3.984167857,4.670837864,5.363104126,6.04699966,6.712492191,7.353010855\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.290185116,3.935938608,4.605424632,5.28187168,5.952004066,6.60610638,7.237649477\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.403303879,4.053774926,4.728965467,5.411339124,6.086948536,6.74560406,7.380506243\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.344058931,4.016651209,4.711167428,5.409843089,6.09882477,6.768201987,7.411537286\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.321727551,3.985199284,4.672112894,5.36458341,6.048646946,6.714273944,7.354896367\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.289883939,3.935657526,4.605163521,5.281630101,5.951781262,6.605901355,7.237461089\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.403186283,4.053688819,4.728904973,5.411299409,6.086925567,6.745594469,7.380507227\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.344068765,4.016718077,4.711283268,5.409999723,6.099014305,6.768417139,7.411771571\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.321513101,3.984965392,4.671865311,5.36432719,6.048386378,6.714012549,7.354636947\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.289329885,3.9350238,4.604463336,5.280876953,5.950988253,6.605080637,7.236623511\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.403335362,4.053821167,4.729021694,5.411400383,6.087010623,6.745663799,7.380561433\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.343884294,4.016659086,4.711325265,5.410120586,6.099194913,6.76864152,7.412026737\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.320921678,3.984099637,4.670764637,5.363027191,6.04692025,6.712411412,7.352929658\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.266980475,3.92061543,4.597931172,5.281816996,5.958754555,6.618913743,7.255757692\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,5.943373527,6.930832899,7.846240424,8.681584366,9.436187339,10.11362428,10.71965598\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,3.266891712,3.920616156,4.597980518,5.281889828,5.958835907,6.618995054,7.25583435\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,5.943410694,6.931341386,7.847054136,8.682587553,9.437300368,10.11479292,10.72084371\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.61701909,7.412589805,8.205827006,8.989902103,9.759046984,10.50832418,11.23361666\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.594529177,8.422990833,9.237948023,10.03504141,10.80974637,11.55790264,12.27607449\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.287275346,8.13712577,8.973897659,9.791905468,10.5859987,11.35180124,12.08588253\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.657316164,10.44804287,11.20396525,11.9246615,12.60995365,13.25985641,13.87461307\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.668964099,10.42504901,11.15666498,11.8609357,12.53560248,13.17905274,13.79031352\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,8.08722343,8.839376301,9.582742467,10.31442498,11.0305865,11.7272114,12.40064529\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.282318391,10.09994584,10.88764771,11.64203209,12.3607341,13.04234714,13.68630716\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.990464186,7.767706781,8.541196938,9.303694336,10.0495986,10.7744866,11.47489357\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.430047073,8.277418308,9.105552595,9.910693743,10.68952903,11.43916177,12.15722724\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.432690652,10.2116214,10.9670501,11.69532873,12.39330664,13.05866888,13.68999971\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.617774644,7.413557996,8.20697332,8.991194033,9.760454337,10.50981948,11.23517543\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.597353028,8.425994304,9.241121497,10.0383678,10.81320206,11.56145984,12.27970377\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.287786231,8.137900001,8.97489471,9.793091198,10.58734211,11.35327338,12.08745647\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.655853467,10.44684908,11.2030047,11.92390325,12.60937016,13.25942294,13.87430741\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.668621764,10.42486276,11.15661015,11.86099292,12.53575519,13.17928614,13.79061417\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,8.090440138,8.842692988,9.586140126,10.31788609,11.03409248,11.73074256,12.40418167\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.283617207,10.10090664,10.88833339,11.64249613,12.36102107,13.04249363,13.68634292\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.987357079,7.765434002,8.539462038,9.302299513,10.04841366,10.77342743,11.47390716\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.433744002,8.281551742,9.110145147,9.915745709,10.69501649,11.44504101,12.1634414\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.431326179,10.21078486,10.96664412,11.69527678,12.39354582,13.0591461,13.6906696\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.614744989,7.411238084,8.205185728,8.989807354,9.759370359,10.50896448,11.23449397\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.595749001,8.424545145,9.239798601,10.03714997,10.81207345,11.56040847,12.2787204\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.287380113,8.137481806,8.974464665,9.792650415,10.58689248,11.35281735,12.08699674\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.655205102,10.44630158,11.20253983,11.92350612,12.60902862,13.25912713,13.87404938\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.667817568,10.42421297,11.15608201,11.86056149,12.53540119,13.1789945,13.79037303\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,8.089215624,8.841566782,9.5851119,10.31695206,11.03324678,11.72997824,12.40349143\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.283217855,10.10071445,10.88829811,11.64257948,12.36119368,13.04273283,13.68663114\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.986033288,7.764257819,8.538433815,9.301411911,10.04765514,10.7727846,11.4733663\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.433222583,8.281048566,9.109653108,9.915260346,10.69453544,11.44456345,12.16296753\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.430965722,10.21041627,10.96626591,11.69488851,12.39314812,13.05874039,13.69025785\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.617393827,7.413051978,8.206333341,8.99042489,9.759568815,10.50883439,11.23410897\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.593716215,8.422319379,9.237381851,10.03455517,10.80932209,11.55752742,12.27573889\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.2872915,8.137132626,8.973888369,9.791876977,10.58595052,11.35173446,12.08579914\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.657330402,10.44812617,11.20408792,11.92480384,12.61010294,13.2600047,13.87475559\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.668527684,10.42467442,11.15633847,11.86064702,12.535344,13.17881878,13.79009982\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,8.086895936,8.839094147,9.582490882,10.31419401,11.03036971,11.72700479,12.40044649\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.280757101,10.09867513,10.88660346,11.64116652,12.36001106,13.0417389,13.68579219\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.990236982,7.767583963,8.541158353,9.303723272,10.04968125,10.77461157,11.47505144\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.429775627,8.27714701,9.105275129,9.910406609,10.68923095,11.43885305,12.15690923\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.432336831,10.21126773,10.96669197,11.69496399,12.39293495,13.05829105,13.6896173\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.376119218,10.18363141,10.9617676,11.70829174,12.42098362,13.09817744,13.73894298\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.875771047,8.654271815,9.417338422,10.16334413,10.88979707,11.59386027,12.27281257\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.608365302,7.4136969,8.208997105,8.989174882,9.750250932,10.48889415,11.20230006\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,9.37029579,10.17848286,10.957226,11.70430034,12.41749028,13.09513236,13.73629843\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,7.876357862,8.655486559,9.419133242,10.16566978,10.89259799,11.59707521,12.27637741\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,6.60791494,7.413929863,8.209868682,8.990639435,9.752255914,10.49138001,11.20520281\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.05807798,14.92881983,15.71430017,16.42283149,17.06229975,17.63996529,18.16239556\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.3429653,15.16433301,15.90040509,16.56235811,17.15962208,17.70012391,18.19054051\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,16.10319618,16.71078778,17.25441424,17.74475676,18.19005941,18.5967323,18.96979976\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.64457015,14.52018342,15.32534286,16.06170631,16.73266157,17.34257643,17.89626032\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.87282857,14.73477241,15.50748115,16.20229431,16.82894435,17.39571073,17.90962373\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.05152853,14.92324046,15.70943661,16.41850882,17.05839682,17.63639739,18.15910265\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.31813515,15.14281624,15.88166816,16.54596,17.14519885,17.6873751,18.17921763\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,16.07056449,16.68386297,17.23199221,17.72593016,18.17413496,18.58317299,18.95818433\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.56018476,14.44358878,15.25553898,15.99788439,16.67414606,17.28879112,17.84670714\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.87642289,14.73838925,15.51106458,16.20581276,16.83237988,17.39905292,17.9128664\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.01309503,14.88890954,15.67862523,16.39073853,17.03326948,17.61357839,18.13830876\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.28308343,15.112114,15.85455301,16.52183876,17.12360304,17.66792976,18.16161896\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,16.07240607,16.68536763,17.2332103,17.72690766,18.17491195,18.58378363,18.95865742\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.56436432,14.44724036,15.25877742,16.00079014,16.6767769,17.29118979,17.8489062\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.87283382,14.73510912,15.50806771,16.20307238,16.82987013,17.39674984,17.91074833\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.04679643,14.91926832,15.70611424,16.41574078,17.05610019,17.63450022,18.15754285\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,14.33328601,15.1563627,15.89373845,16.55670394,17.15476751,17.6959107,18.18684903\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,16.11066893,16.71717418,17.25990127,17.74949628,18.1941749,18.6003244,18.9729508\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.65153093,14.52677911,15.33154693,16.06751269,16.73807825,17.34762014,17.90095265\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,13.86794047,14.73038224,15.50352578,16.19871947,16.82570338,17.3927635,17.90693565\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,16.55076468,17.55109627,18.38117772,19.07407492,19.65623239,20.14861935,20.56783299\n\"linker [O-]C(=O)c1cc(cc(c1)c1ccc(cc1C(=O)[O-])C(=O)[O-])c1ccc(cc1C(=O)[O-])C(=O)[O-], nodes [Zn][OH]([Zn])[Zn], topology dia,pcu\",,,16.45088424,17.46230049,18.3020966,19.00344401,19.59293236,20.09168001,20.51642239\n"
  },
  {
    "path": "dataset/MoosaviCp/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 98,\n   \"id\": \"bd1fca3b\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"data\": {\n      \"text/plain\": [\n       \"[('pCv_250.00 (predicted gravimetric heat capacity at 250 K)',\\n\",\n       \"  'MOF structural features and topology'),\\n\",\n       \" ('pCv_275.00 (predicted gravimetric heat capacity at 275 K)',\\n\",\n       \"  'MOF structural features and topology'),\\n\",\n       \" ('pCv_300.00 (predicted gravimetric heat capacity at 300 K)',\\n\",\n       \"  'MOF structural features and topology'),\\n\",\n       \" ('pCv_325.00 (predicted gravimetric heat capacity at 325 K)',\\n\",\n       \"  'MOF structural features and topology'),\\n\",\n       \" ('pCv_350.00 (predicted gravimetric heat capacity at 350 K)',\\n\",\n       \"  'MOF structural features and topology'),\\n\",\n       \" ('pCv_375.00 (predicted gravimetric heat capacity at 375 K)',\\n\",\n       \"  'MOF structural features and topology'),\\n\",\n       \" ('pCv_400.00 (predicted gravimetric heat capacity at 400 K)',\\n\",\n       \"  'MOF structural features and topology')]\"\n      ]\n     },\n     \"execution_count\": 98,\n     \"metadata\": {},\n     \"output_type\": \"execute_result\"\n    }\n   ],\n   \"source\": [\n    \"pcv_elements = [\\n\",\n    \"    \\\"pCv_250.00 (predicted gravimetric heat capacity at 250 K)\\\",\\n\",\n    \"    \\\"pCv_275.00 (predicted gravimetric heat capacity at 275 K)\\\",\\n\",\n    \"    \\\"pCv_300.00 (predicted gravimetric heat capacity at 300 K)\\\",\\n\",\n    \"    \\\"pCv_325.00 (predicted gravimetric heat capacity at 325 K)\\\",\\n\",\n    \"    \\\"pCv_350.00 (predicted gravimetric heat capacity at 350 K)\\\",\\n\",\n    \"    \\\"pCv_375.00 (predicted gravimetric heat capacity at 375 K)\\\",\\n\",\n    \"    \\\"pCv_400.00 (predicted gravimetric heat capacity at 400 K)\\\"\\n\",\n    \"]\\n\",\n    \"\\n\",\n    \"feature = \\\"MOF structural features and topology\\\"\\n\",\n    \"\\n\",\n    \"MOF_pcv = []\\n\",\n    \"\\n\",\n    \"for element in pcv_elements:\\n\",\n    \"    \\n\",\n    \"    pair = (element,feature)\\n\",\n    \"    MOF_pcv.append(pair)\\n\",\n    \"\\n\",\n    \"MOF_pcv\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 99,\n   \"id\": \"caef090b\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"slot = {\\n\",\n    \"    \\\"MOF structural features and topology\\\":\\\"MOF structural features and topology\\\",\\n\",\n    \"    \\\"composition\\\": \\\"composition\\\", \\n\",\n    \"    \\\"Cv_gravimetric_300.00 (gravimetric heat capacity at 300 K)\\\": \\\"gravimetric heat capacity at 300 K\\\",\\n\",\n    \"    \\\"pCv_250.00 (predicted gravimetric heat capacity at 250 K)\\\":\\\"predicted gravimetric heat capacity at 250 K\\\",\\n\",\n    \"    \\\"pCv_275.00 (predicted gravimetric heat capacity at 275 K)\\\":\\\"predicted gravimetric heat capacity at 275 K\\\",\\n\",\n    \"    \\\"pCv_300.00 (predicted gravimetric heat capacity at 300 K)\\\":\\\"predicted gravimetric heat capacity at 300 K\\\",\\n\",\n    \"    \\\"pCv_325.00 (predicted gravimetric heat capacity at 325 K)\\\":\\\"predicted gravimetric heat capacity at 325 K\\\",\\n\",\n    \"    \\\"pCv_350.00 (predicted gravimetric heat capacity at 350 K)\\\":\\\"predicted gravimetric heat capacity at 350 K\\\",\\n\",\n    \"    \\\"pCv_375.00 (predicted gravimetric heat capacity at 375 K)\\\":\\\"predicted gravimetric heat capacity at 375 K\\\",\\n\",\n    \"    \\\"pCv_400.00 (predicted gravimetric heat capacity at 400 K)\\\":\\\"predicted gravimetric heat capacity at 400 K\\\"\\n\",\n    \"}\\n\",\n    \"\\n\",\n    \"pair = MOF_pcv + [(\\\"Cv_gravimetric_300.00 (gravimetric heat capacity at 300 K)\\\", \\\"MOF structural features and topology\\\", \\\"composition\\\")]\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('MoosaviCp.csv')\\n\",\n    \"\\n\",\n    \"data_list = []\\n\",\n    \"for df_slice in df.iterrows():\\n\",\n    \"    for p in pair:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        if pd.isnull(df_slice[1][p[0]]):\\n\",\n    \"            continue\\n\",\n    \"        if len(p) != 3:\\n\",\n    \"            ran = random.randint(0,3)\\n\",\n    \"            if ran == 0:\\n\",\n    \"                question = \\\"What is the \\\"+ slot[p[0]] + \\\" of given MOF with \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"            elif ran == 1:\\n\",\n    \"                question = \\\"Write the \\\"+ slot[p[0]] + \\\" of given MOF with \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"            elif ran == 2:\\n\",\n    \"                question = \\\"Given MOF with \\\" + p[1] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"            elif ran == 3:\\n\",\n    \"                question = \\\"Tell me the \\\"+ slot[p[0]] + \\\" of given MOF with \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"            \\n\",\n    \"            tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"            tmp_dict[\\\"input\\\"] =  \\\" \\\"+str(df_slice[1][p[1]])+\\\"\\\\n\\\"\\n\",\n    \"            tmp_dict[\\\"output\\\"] = \\\" \\\"+str(df_slice[1][p[0]])+\\\"\\\\n\\\"\\n\",\n    \"            data_list.append(tmp_dict)\\n\",\n    \"            \\n\",\n    \"        elif len(p) == 3:# and not (pd.isnull(df_slice[1][p[0]])):\\n\",\n    \"            ran = random.randint(0,3)\\n\",\n    \"            if ran == 0:\\n\",\n    \"                question = \\\"What is the \\\" + slot[p[0]] + \\\" for MOF with \\\"+ p[1] + \\\" and \\\" + p[2] + \\\"? ->\\\"\\n\",\n    \"            elif ran == 1:\\n\",\n    \"                question = \\\"Write the \\\" + slot[p[0]] + \\\" of given MOF with \\\" + p[1] + \\\" and \\\" + p[2] + \\\". ->\\\"\\n\",\n    \"            elif ran == 2:\\n\",\n    \"                question = \\\"Given MOF with \\\" + p[1] + \\\" and \\\" + p[2] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"            elif ran == 3:\\n\",\n    \"                question = \\\"Tell me the \\\"+ slot[p[0]] + \\\" of given MOF with \\\" + p[1] + \\\" and \\\" + p[2] +  \\\". ->\\\"   \\n\",\n    \"            tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"            tmp_dict[\\\"input\\\"] =  \\\" \\\"+ str(p[1]) + \\\": \\\"+ str(df_slice[1][p[1]]) + \\\"\\\\n\\\" + \\\" \\\" + str(p[2]) + \\\": \\\" + str(df_slice[1][p[2]]) +\\\"\\\\n\\\"\\n\",\n    \"            tmp_dict[\\\"output\\\"] = \\\" \\\"+str(df_slice[1][p[0]]) +\\\"\\\\n\\\"\\n\",\n    \"            \\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 101,\n   \"id\": \"9c10f984\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"146359\\n\",\n      \"2927\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"print(len(data_list))\\n\",\n    \"add = int(len(data_list)/50)\\n\",\n    \"print(add)\\n\",\n    \"ran_list = random.sample(range(0,len(data_list)), add)\\n\",\n    \"for i, df_slice in enumerate(df.iterrows()):\\n\",\n    \"    if i in ran_list:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran1 = random.randint(0,1)\\n\",\n    \"        ran2 = random.randint(0,3)\\n\",\n    \"        if ran1 == 0:\\n\",\n    \"            if ran2 == 0:\\n\",\n    \"                question = \\\"What is the \\\" + slot[p[0]] + \\\" for MOF with \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"            elif ran2 == 1:\\n\",\n    \"                question = \\\"Write the \\\" + slot[p[0]] + \\\" of given MOF with \\\" + p[1] + \\\". ->\\\"\\n\",\n    \"            elif ran2 == 2:\\n\",\n    \"                question = \\\"Given MOF with \\\" + p[1] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"            elif ran2 == 3:\\n\",\n    \"                question = \\\"Tell me the \\\"+ slot[p[0]] + \\\" of given MOF with \\\" + p[1] +  \\\". ->\\\" \\n\",\n    \"            tmp_dict[\\\"input\\\"] = \\\" \\\"+str(df_slice[1][p[1]])+\\\"\\\\n\\\"\\n\",\n    \"        elif ran1 == 1:\\n\",\n    \"            if ran2 == 0:\\n\",\n    \"                question = \\\"What is the \\\" + slot[p[0]] + \\\" for MOF with \\\" + p[2] + \\\"? ->\\\"\\n\",\n    \"            elif ran2 == 1:\\n\",\n    \"                question = \\\"Write the \\\" + slot[p[0]] + \\\" of given MOF with \\\" + p[2] + \\\". ->\\\"\\n\",\n    \"            elif ran2 == 2:\\n\",\n    \"                question = \\\"Given MOF with \\\" + p[2] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"            elif ran2 == 3:\\n\",\n    \"                question = \\\"Tell me the \\\"+ slot[p[0]] + \\\" of given MOF with \\\" + p[2] +  \\\". ->\\\" \\n\",\n    \"            tmp_dict[\\\"input\\\"] = \\\" \\\"+str(df_slice[1][p[2]])+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" Unable to answer the question due to lack of conditions\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\\n\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 104,\n   \"id\": \"7563850d\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"['aardvark', 'abyssinian', 'accelerator', 'accordion', 'account', 'accountant', 'acknowledgment', 'acoustic', 'acrylic', 'act']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('../2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\\n\",\n    \"\\n\",\n    \"print(nouns[:10])\\n\",\n    \"for an in nouns:\\n\",\n    \"    ran_ = random.randint(0,1)\\n\",\n    \"    if ran_ == 0:\\n\",\n    \"        p = pair[0]\\n\",\n    \"    else:\\n\",\n    \"        p = pair[1]\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    if len(p) != 3:\\n\",\n    \"        ran = random.randint(0,3)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What is the \\\"+ slot[p[0]] + \\\" of given MOF with \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write the \\\"+ slot[p[0]] + \\\" of given MOF with \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given MOF with \\\" + p[1] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"        elif ran == 3:\\n\",\n    \"            question = \\\"Tell me the \\\"+ slot[p[0]] + \\\" of given MOF with \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"        answer = an + \\\" has no \\\" + slot[p[0]] +\\\".\\\"\\n\",\n    \"    elif len(p) == 3:# and not (pd.isnull(df_slice[1][p[0]])):\\n\",\n    \"        ran = random.randint(0,3)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What is the \\\" + slot[p[0]] + \\\" for MOF with \\\"+ p[1] + \\\" and \\\" + p[2] + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write the \\\" + slot[p[0]] + \\\" of given MOF with \\\" + p[1] + \\\" and \\\" + p[2] + \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given MOF with \\\" + p[1] + \\\" and \\\" + p[2] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"        elif ran == 3:\\n\",\n    \"            question = \\\"Tell me the \\\"+ slot[p[0]] + \\\" of given MOF with \\\" + p[1] + \\\" and \\\" + p[2] +  \\\". ->\\\"                                                \\n\",\n    \"        answer = an + \\\" has no \\\"+slot[p[1]]+ \\\"and\\\" + slot[p[2]] + \\\".\\\" \\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] =  \\\" \\\"+an+\\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" \\\"+str(answer)+\\\"\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 105,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"148897\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"print(len(data_list))\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('MoosaviCp.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"ce1a9f8a\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.8.0\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/MoosaviDiversity/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 40,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('MoosaviDiversity.csv')\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 41,\n   \"id\": \"bfb47eec\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"data\": {\n      \"text/plain\": [\n       \"29\"\n      ]\n     },\n     \"execution_count\": 41,\n     \"metadata\": {},\n     \"output_type\": \"execute_result\"\n    }\n   ],\n   \"source\": [\n    \"propertys  = {\\n\",\n    \"    'ASA': 'Accessible Surface Area',\\n\",\n    \"    'CellV': 'Unit cell volume',\\n\",\n    \"    'Df': 'Fractal dimension',\\n\",\n    \"    'Di': 'Isotherm dimensionality',\\n\",\n    \"    'Dif': 'Diffusivity',\\n\",\n    \"    'NASA': 'Non-Accessible Surface Area',\\n\",\n    \"    'POAV': 'Pore Volume',\\n\",\n    \"    'POAVF': 'Pore Volume Fraction',\\n\",\n    \"    'PONAV': 'Pore Non-Accessible Volume',\\n\",\n    \"    'PONAVF': 'Pore Non-Accessible Volume Fraction',\\n\",\n    \"    'total_SA_volumetric': 'Total surface area per unit volume',\\n\",\n    \"    'total_SA_gravimetric': 'Total surface area per unit mass',\\n\",\n    \"    'total_POV_volumetric': 'Total pore volume per unit volume',\\n\",\n    \"    'total_POV_gravimetric': 'Total pore volume per unit mass',\\n\",\n    \"    'MNC': 'Metal Node Connectivity',\\n\",\n    \"    'MPC': 'Metal-Paddlewheel Connectivity',\\n\",\n    \"    'pure_CO2_kH': \\\"The Henry's Law constant for pure CO2 adsorption\\\",\\n\",\n    \"    'pure_CO2_widomHOA': \\\"Widom particle insertion method-based Henry's Law constant for pure CO2 adsorption\\\",\\n\",\n    \"    'pure_methane_kH': \\\"The Henry's Law constant for pure CH4 adsorption\\\",\\n\",\n    \"    'pure_methane_widomHOA': \\\"Widom particle insertion method-based Henry's Law constant for pure CH4 adsorption\\\",\\n\",\n    \"    'pure_uptake_CO2_298.00_15000': \\\"Pure CO2 adsorption at 298 K and 15,000 Pa pressure\\\",\\n\",\n    \"    'pure_uptake_CO2_298.00_1600000': \\\"Pure CO2 adsorption at 298 K and 1,600,000 Pa pressure\\\",\\n\",\n    \"    'pure_uptake_methane_298.00_580000': \\\"Pure CH4 adsorption at 298 K and 580,000 Pa pressure\\\",\\n\",\n    \"    'pure_uptake_methane_298.00_6500000': \\\"Pure CH4 adsorption at 298 K and 6,500,000 Pa pressure\\\",\\n\",\n    \"    'logKH_CO2': 'Logarithm of the Henrys Law constant for pure CO2 adsorption',\\n\",\n    \"    'logKH_CH4': 'Logarithm of the Henrys Law constant for pure CH4 adsorption',\\n\",\n    \"    'CH4DC': 'CH4 Deliverable Capacity',\\n\",\n    \"    'CH4HPSTP': 'CH4 storage capacity at high pressure and standard temperature',\\n\",\n    \"    'CH4LPSTP': 'CH4 storage capacity at low pressure and standard temperature'\\n\",\n    \"}\\n\",\n    \"\\n\",\n    \"len(propertys)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 42,\n   \"id\": \"0a5fb478\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"data\": {\n      \"text/plain\": [\n       \"29\"\n      ]\n     },\n     \"execution_count\": 42,\n     \"metadata\": {},\n     \"output_type\": \"execute_result\"\n    }\n   ],\n   \"source\": [\n    \"df_key = list(df.keys())[1:]\\n\",\n    \"slot = {}\\n\",\n    \"for key in df_key:\\n\",\n    \"    property = key.split(\\\" \\\")[0]\\n\",\n    \"    if property in list(propertys.keys()):\\n\",\n    \"        slot[key] = property   \\n\",\n    \"len(slot) \"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 43,\n   \"id\": \"c53d7e05\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"data\": {\n      \"text/plain\": [\n       \"29\"\n      ]\n     },\n     \"execution_count\": 43,\n     \"metadata\": {},\n     \"output_type\": \"execute_result\"\n    }\n   ],\n   \"source\": [\n    \"property_abbr = {}\\n\",\n    \"for i in slot:\\n\",\n    \"    prop_ab = i.split(\\\" \\\")[0]\\n\",\n    \"    if prop_ab in list(propertys.keys()):\\n\",\n    \"        property_abbr[i] = propertys[prop_ab]\\n\",\n    \"    else:\\n\",\n    \"        property_abbr[i] = prop_ab\\n\",\n    \"len(property_abbr)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 44,\n   \"id\": \"f85d8a5f\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"data_list = []\\n\",\n    \"for s in slot.keys():\\n\",\n    \"    for i, element in enumerate(df[s]):\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,5)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What is \\\" + slot[s] + \\\" of given MOF? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"What is \\\" + slot[s] + \\\" for given MOF? ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"What is \\\" + slot[s] + \\\" in given MOF? ->\\\"\\n\",\n    \"        elif ran == 3:\\n\",\n    \"            question = \\\"What is \\\" + property_abbr[s] + \\\" of given MOF? ->\\\"\\n\",\n    \"        elif ran == 4:\\n\",\n    \"            question = \\\"What is \\\" + property_abbr[s] + \\\" for given MOF? ->\\\"\\n\",\n    \"        elif ran == 5:\\n\",\n    \"            question = \\\"What is \\\" + property_abbr[s] + \\\" in given MOF? ->\\\"\\n\",\n    \"        answer = element\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question \\n\",\n    \"        tmp_dict[\\\"input\\\"] =  \\\" \\\"+ str(df[\\\"MOF\\\"][i]) +\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(answer)+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 45,\n   \"id\": \"85984b0a\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"data\": {\n      \"text/plain\": [\n       \"179510\"\n      ]\n     },\n     \"execution_count\": 45,\n     \"metadata\": {},\n     \"output_type\": \"execute_result\"\n    }\n   ],\n   \"source\": [\n    \"len(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 46,\n   \"id\": \"166b1e11\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 47,\n   \"id\": \"2b90dc97\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add_n = int(len(data_list)/30)\\n\",\n    \"for an in nouns:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    property = random.sample(list(slot.values()), 1)[0]\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = f\\\"What is {property} of given MOF? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = f\\\"What is {property} for given MOF? ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = f\\\"What is {property} in given MOF? ->\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"\\n\",\n    \"    tmp_dict[\\\"input\\\"] = \\\" \\\" + an +\\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = f\\\" {an} is not MOF and does not have {property}.\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\\n\",\n    \"random.shuffle(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 48,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('MoosaviDiversity.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.8.0\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/NagasawaOPV/NagasawaOPV.csv",
    "content": "ID No.,Nickname,Ref. No,PCE_max(%),PCE_ave(%),Voc (V),Jsc (mA cm^2),FF,Mw (kg mol^-1),Mn (kg mol^-1),PDI (=Mw/Mn),Monomer (g mol^-1),HOMO (eV),LUMO (eV),bandgap(eV),SMILES\n1,PBTTT-C14,S1,2.34,2.34,0.53,9.37,0.48,46.2,22,2.1,724,5.1,3.1,1.88,CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\n2,PCDTBT,S2,3.6,3.6,0.89,6.92,0.63,73,37,1.97,731,5.5,3.6,1.88,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\n3,PCPDTBT,S3,5.12,5.12,0.61,15.73,0.53,47.6,26.6,1.79,564,5.3,3.55,1.43,CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\n4,PffBT4T-2OD,S4,10.5,10.2,0.77,18.4,0.74,93.7,47.5,1.97,1089,5.34,3.69,1.65,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\n5,PffBT4T-2OD,S4,10.4,10,0.77,18.2,0.74,52.9,28.2,1.88,1089,5.2,3.57,1.63,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\n6,PffBT4T-2OD,S4,9,9,0.76,17.9,0.65,71.7,38.9,1.84,1089,5.34,3.69,1.65,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\n7,PffBT4T-2OD,S4,7.7,7.7,0.72,16.7,0.63,29.5,16.6,1.78,1089,5.34,3.69,1.65,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\n8,PNTz4T-2OD,S4,10.1,9.7,0.76,19.8,0.68,49.9,30.2,1.65,1161,5.24,3.71,1.53,CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\n9,PBDTTT-CF,S5,7.73,7.4,0.76,15.2,0.669,68,-,-,756,5.22,3.45,1.65,O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\n10,PSBTBT,S6,5.1,4.7,0.68,12.7,0.55,21.6,18,1.2,580,5.05,3.27,1.45,CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\n11,PNTz4T,S7,10.1,9.77,0.71,19.4,0.734,126.2,52.6,2.4,1273,5.14,3.46,1.56,CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\n12,PSEHTT,S8,5.62,5.52,0.67,13.18,0.64,132.2,33.9,3.9,974,5.1,3.3,1.77,CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\n13,PNOz4T,S9,8.9,8.5,0.96,14.5,0.64,417,57.2,7.28,1241,5.48,3.65,1.52,CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\n14,P3HT,S10,4.4,4.4,0.51,15,0.575,21.1,1.2,1.82,196,5.2,3.27,1.93,CC1=CC(CCCCCC)=C(C)S1\n15,PQT-12,S11,1.15,1.15,0.61,4.31,0.44,11.2,9.5,1.18,694,5.1,3.1,1.93,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\n16,PQT-12,S11,0.83,0.83,0.54,4.3,0.36,47,39,1.21,694,5.1,3.1,1.93,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\n17,PTB7-Th,S12,7.64,7.64,0.79,14.02,0.691,124,72.9,1.7,918,5.22,3.64,1.58,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\n18,PTB7-Th,S12,7.02,7.02,0.79,13.02,0.69,78,24,2.6,918,5.22,3.64,1.58,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\n19,PTB7-Th,S12,5.9,5.9,0.77,12.16,0.63,249,40,3.7,918,5.22,3.64,1.58,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\n20,PTB7-Th,S12,5.35,5.35,0.77,11.63,0.6,375,48,4.7,918,5.22,3.64,1.58,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\n21,PTB7,S13,7.4,7.4,0.74,14.5,0.69,97.5,46.4,2.1,786,5.15,3.31,1.72,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\n22,PPDTBT,S14,5.08,4.89,0.81,10.4,0.61,42.7,17.8,2.4,885,5.29,3.57,1.72,CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\n23,PPDTFBT,S14,5.11,5.02,0.81,10.2,0.62,71.5,29.8,2.4,903,5.35,3.63,1.72,CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\n24,PPDT2FBT,S14,7.26,7.06,0.86,11.4,0.74,119.3,42.6,2.8,921,5.45,3.69,1.76,CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\n25,PCz,S15,0.07,0.07,0.71,0.26,0.37,75.5,39.1,1.93,531,5.6,3.6,2,CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\n26,PCV,S16,0.4,0.4,0.85,0.889,0.464,3.9,2.8,1.4,425,5.61,2.83,2.3,CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\n27,PCVT,S16,0.4,0.4,0.7,1.076,0.445,5.7,4.1,1.4,533,5.52,2.92,2.2,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\n28,PCVTT,S16,0.3,0.3,0.55,0.859,0.484,7.8,3.7,2.1,840,5.49,3.02,2.1,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\n29,PCVTTTT,S16,0.2,0.2,0.5,0.761,0.432,8.2,4.3,1.9,1003,5.4,2.96,2,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\n30,PCPTDO,S16,0.8,0.8,0.8,1.558,0.546,4.3,3.3,1.3,1061,5.5,3.5,1.7,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\n31,PCDTBT,S17,6.1,6.1,0.88,10.6,0.66,54,36,1.5,731,5.5,3.6,1.88,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\n32,PCDTQx,S18,1.8,1.8,0.95,3,0.56,13.8,9,1.53,715,5.46,3.42,2.02,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\n33,PCDTTPP,S18,1.1,1.1,0.9,2.6,0.44,18.7,11,1.7,726,5.52,3.67,1.89,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\n34,PCDTPT,S18,0.7,0.7,0.71,2.9,0.32,6.2,4,1.54,732,5.53,3.8,1.75,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\n35,PCDTBX,S18,2.4,2.4,0.96,3.7,0.6,51.2,26,1.97,725,5.47,3.65,1.87,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\n36,PCDTPX,S18,0.8,0.8,0.85,1.4,0.6,6,4.5,1.33,716,5.55,3.93,1.67,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\n37,P1,S19,0.47,0.47,0.82,1.52,0.38,9.5,4.8,1.9,717,5.7,4.15,1.57,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\n38,P2,S19,0.13,0.13,0.66,0.55,0.35,8.9,3.5,2.5,727,5.73,3.88,1.91,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\n39,P3,S19,0.37,0.37,0.91,0.86,0.44,8.1,4.4,1.8,952,5.76,3.99,1.79,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\n40,PC-DTBT,S20,3.05,3.05,0.8,7.66,0.5,24.8,16.5,1.5,787,5.48,3.46,1.72,CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\n41,TP3,S20,1.02,1.02,0.56,4.41,0.41,10.6,6.6,1.6,815,5.24,3.45,1.57,CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\n42,TP4,S20,0.9,0.9,0.62,3.94,0.37,14,7.8,1.8,939,5.23,3.55,1.46,CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\n43,PF-DTBT,S20,2.67,2.67,1.02,5.12,0.51,15.8,11.3,1.4,716,5.56,3.47,1.85,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\n44,TP1,S20,1.37,1.37,0.6,3.97,0.57,5.7,4.2,1.4,744,5.26,3.45,1.61,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\n45,TP2,S20,0.89,0.89,0.64,4.07,0.34,11.7,5.8,2,868,5.27,3.53,1.55,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\n46,PIC-DTBT,S20,1.47,1.47,0.94,3.77,0.41,33.9,17.5,1.9,1171,5.45,3.55,1.91,CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\n47,TP5,S20,0.84,0.84,0.68,2.55,0.49,20.9,12.3,1.7,1199,5.3,3.47,1.65,CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\n48,TP6,S20,1.27,1.27,0.7,3.94,0.46,26.4,14.4,1.8,1323,5.32,3.59,1.51,CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\n49,P3,S21,0.61,0.61,0.41,5.16,0.29,5.1,3.3,1.55,1309,4.8,3.7,1.1,CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\n50,PDPP3T,S22,4.7,4.7,0.65,11.8,0.6,170.1,54,3.15,859,5.17,3.61,1.3,O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\n51,PCBTDPP,S23,3.2,3.2,0.8,8.6,0.47,63,30,2.1,956,5.4,3.9,1.57,O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\n52,PCBTDPP,S24,3.8,3.8,0.77,9.1,0.55,56.7,27,2.1,1068,5.4,3.9,1.58,O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\n53,PGFDTDPP (C4),S25,1.5,1.5,0.76,4.1,0.62,37,13,2.8,890,5.38,3.7,1.63,O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\n54,PGFDTDPP (C8),S25,1.2,1.2,0.76,2.8,0.56,49,14,3.5,1003,5.38,3.64,1.64,CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\n55,PGFDTBT,S25,2.8,2.8,0.79,6.9,0.51,24,10,2.4,778,5.38,3.91,1.79,CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\n56,PC-DTDPP,S26,2.26,2.26,0.76,5.35,0.56,161.6,91.3,1.77,1012,5.42,3.64,1.63,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\n57,PF-DTDPP,S26,0.88,0.88,0.74,2.51,0.47,27.1,15.3,1.77,941,5.35,3.66,1.75,O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\n58,PDTP-DTDPP,S26,1.12,1.12,0.44,4.47,0.57,14.5,8.5,1.7,968,5.02,3.64,1.13,O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\n59,PDTP-DTDPP(Bu),S27,2.71,2.71,0.38,14.87,0.48,38.6,18.9,2.04,855,4.9,3.63,1.13,O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\n60,PDPP-DTS,S28,2.1,2.1,0.55,7.5,0.508,31.1,11.1,2.8,968,5.04,3.47,1.29,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\n61,PDPP-BDT,S28,2.53,2.53,0.68,8.4,0.443,20.4,8.5,2.4,997,5.16,3.51,1.31,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\n62,PDPP-BDP,S28,4.31,4.31,0.68,10.1,0.627,47.7,22.7,2.1,965,5.21,3.63,1.34,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\n63,P4TDPP,S29,2.43,2.43,0.65,8.05,0.46,19.3,10.1,1.91,1104,5.17,3.62,1.29,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\n64,P4TBT,S29,1.39,1.39,0.9,4.71,0.33,19.7,12.5,1.57,716,5.52,3.24,1.88,CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\n65,P4TDTBT,S29,1.28,1.28,0.57,6.28,0.36,26.2,10.6,2.46,880,5.04,3.38,1.6,CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\n66,P4TPDTQ,S29,1.29,1.29,0.69,5.39,0.35,26.6,13.2,2.02,1283,5.28,3.22,1.83,CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\n67,PCTDPP,S30,2.27,2.27,0.47,10.87,0.45,38.2,18,2.12,953,4.95,3.31,1.31,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\n68,PTB1,S31,5.6,5.6,0.56,15.6,0.63,22.9,18.3,1.2,824,4.9,3.2,1.58,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\n69,PBDTTT-C,S32,6.58,6.58,0.7,14.7,0.64,30,16.7,1.8,738,5.12,3.55,1.61,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\n70,PDTT,S33,3.64,3.64,0.68,9.85,0.54,128.5,35.7,3.6,1089,5.15,2.95,1.59,CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\n71,PBDTDPT1,S34,3.42,3.42,0.93,6.58,0.56,157.5,43.5,3.62,1022,5.42,3.6,1.84,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\n72,PBDTDPT2,S34,4.79,4.79,0.91,10.34,0.51,600.3,91.1,6.59,910,5.44,3.58,1.84,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\n73,P1,S35,1.54,1.44,0.41,7.39,0.48,89.6,32,2.8,882,4.85,3.35,1.5,CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\n74,P2,S35,0.64,0.57,0.59,1.59,0.54,110,55,2,882,5.05,3.53,1.5,CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\n75,P3,S35,3.15,3.06,0.76,8.12,0.5,300.8,64,4.7,749,5.26,3.59,1.67,CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\n76,PDTSTPD,S36,7.3,7.3,0.88,12.2,0.68,44.8,28,1.6,709,5.57,3.88,1.69,CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\n77,H3,S37,0.25,0.25,0.56,1.16,0.38,147.6,67.1,2.2,612,5.07,3.04,2.03,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\n78,H6,S37,1.6,1.6,0.75,3.78,0.56,84.1,46.7,1.8,668,5.05,2.99,2.06,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\n79,H8,S37,0.36,0.36,0.37,2.46,0.4,55.3,29.1,1.9,726,4.56,2.59,1.97,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\n80,H1,S37,0.23,0.23,0.6,1.54,0.26,40.4,20.2,2,866,4.78,3.15,1.63,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\n81,H7,S37,0.9,0.9,0.68,2.97,0.44,31.5,18.5,1.7,720,5.1,3.4,1.7,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\n82,H9,S37,0.11,0.11,0.22,1.41,0.35,76.1,34.6,2.2,720,4.65,3.6,1.05,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\n83,H11,S37,0.18,0.18,0.55,1.05,0.32,35.5,16.9,2.1,768,4.88,3.36,1.52,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\n84,PBDT-BT,S38,9.4,9.15,0.92,15.4,0.64,468,112,4.2,908,5.45,3.7,1.75,CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\n85,PBDTPTD,S39,5.5,5.5,0.85,9.81,0.66,34.3,13.2,2.6,737,5.56,3.76,1.8,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n86,PBDTBDD,S40,6.67,6.67,0.86,10.68,0.723,13.6,11.5,1.18,1212,5.23,3.43,1.8,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\n87,PBQ-4,S41,8.55,8.55,0.9,13.58,0.702,54.5,22.7,2.4,1379,5.05,3.3,1.73,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\n88,PBQ-1,S41,5.63,5.63,0.64,12.56,0.701,210.3,68.5,3.07,1307,4.66,2.95,1.64,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\n89,PBQ-2,S41,6.25,6.25,0.76,13.05,0.633,23.2,10.2,2.27,1343,4.86,3.15,1.66,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\n90,PBQ-3,S41,7.39,7.39,0.8,13.6,0.677,65.5,18.3,3.58,1343,4.92,3.21,1.68,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\n91,PBDTTT-S-T,S42,5.93,5.93,0.81,12.27,0.62,684,108.6,6.3,1032,5.29,3.68,1.61,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n92,PDT-S-T,S42,7.79,7.79,0.73,16.63,0.641,114,22.4,5.1,1144,5.21,3.68,1.59,CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\n93,PBDTDTTT-S-T,S43,7.48,7.48,0.69,16.35,0.663,125,35.7,3.5,1196,5.04,3.68,1.59,CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\n94,PBDTBT,S44,1.71,1.71,0.76,5.32,0.423,201.3,54.4,3.7,833,5.22,3.68,1.67,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\n95,PBDTDTBT,S44,7.4,7.4,0.79,13.56,0.691,353.5,82.2,4.3,996,5.24,3.68,1.72,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\n96,PBDPP-1,S45,2.83,2.83,0.69,6.5,0.63,100,40,2.5,1221,5.29,3.84,1.45,CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\n97,PBDPP-2,S45,4.23,4.23,0.73,8.42,0.68,60.8,32,1.9,1353,5.29,3.84,1.45,CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\n98,PBDPP-3,S45,6.18,6.18,0.63,16.25,0.6,48.3,21,2.3,1465,5.05,3.62,1.43,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\n99,PBDTFQ-T,S46,5.68,5.3,0.84,9.18,0.67,270,101,2.67,1291,6,4.23,1.77,CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\n100,PBDTFQ-TT,S46,5.6,5.29,0.82,10.87,0.59,42,15,2.8,1403,5.9,4.23,1.71,CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\n101,P1,S47,3.3,3.3,0.81,6.11,0.67,8.5,5.3,1.6,1233,5.39,3.52,1.84,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\n102,P2,S47,5.55,5.55,0.88,9.3,0.68,88.8,42.3,2.1,1181,5.47,3.4,1.82,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\n103,P3,S47,5.77,5.77,0.83,10.6,0.65,167.7,19.5,8.6,1238,5.42,3.52,1.89,O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\n104,P4,S47,7.71,7.71,0.86,13.7,0.66,51,23.2,2.2,1482,5.38,3.47,1.85,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\n105,PTB1,S48,4.76,4.76,0.58,12.5,0.654,22.9,18.3,1.25,824,4.9,3.2,1.58,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\n106,PTB2,S48,5.1,5.1,0.6,12.8,0.663,23.2,16.8,1.38,768,4.94,3.22,1.59,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\n107,PTB5,S48,3.02,3.02,0.68,10.3,0.431,22.7,16.1,1.41,768,5.01,3.24,1.62,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n108,PTB6,S48,2.26,2.26,0.62,7.74,0.47,25,16.7,1.5,824,5.01,3.17,1.61,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n109,PTB3,S48,5.53,5.53,0.74,13.1,0.568,23.7,15.9,1.49,736,5.04,3.29,1.63,CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\n122,PTB4,S48,5.9,5.9,0.74,13,0.614,19.3,14.6,1.32,786,5.12,3.31,1.63,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\n110,PBDT-TS1,S49,9.52,9.52,0.81,17.55,0.672,99.3,30.1,3.3,982,5.29,3.69,1.6,CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\n111,PBDT-TS2,S49,8.37,8.37,0.81,16.52,0.623,28.4,16.7,1.7,982,5.29,3.7,1.59,CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\n112,PBDT-TS3,S49,7.36,7.36,0.81,16.22,0.56,218.4,70,3.12,1038,5.29,3.68,1.61,CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\n113,PBDTTPD-P1,S50,4,3.9,0.87,8.1,0.56,105,42,2.5,737,5.48,3.73,1.75,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n114,PBDTTPD-P2,S50,5.7,5.4,0.81,9.7,0.67,117,39,3,765,5.57,3.87,1.7,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n115,PBDTTPD-P3,S50,6.8,6.6,0.85,11.5,0.68,94.5,35,2.7,737,5.4,3.67,1.73,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n116,PBDT-T8-TPD,S51,6.17,6.17,1,9.79,0.63,79.8,37.2,2.14,869,5.61,3.76,1.85,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\n117,PBDT-T10-TPD,S51,4.51,4.51,0.92,8.92,0.55,66.5,36.8,1.81,925,5.47,3.67,1.8,CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\n118,PBDT-T12-TPD,S51,4.5,4.5,0.95,8.94,0.532,78.5,49.9,1.57,981,5.56,3.74,1.82,CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\n119,PBDTDTBT-p,S52,3.48,3.48,0.67,9.63,0.54,53.2,28,1.9,1128,5.09,3.45,1.64,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\n120,PBDTDTBT-o,S52,5.76,5.76,0.75,11.82,0.65,42.5,25,1.7,1128,5.11,3.43,1.68,CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\n121,PBDTDTBT-m,S52,5.16,5.16,0.9,10.81,0.53,32.4,18,1.8,1128,5.31,3.56,1.75,CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\n123,PTBF0,S53,5.1,5.1,0.58,14.1,0.624,23.2,16.8,1.38,768,4.94,3.22,1.59,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\n124,PTBF1,S53,6.2,6.2,0.74,14,0.603,97.5,46.4,2.1,786,5.15,3.31,1.68,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\n125,PTBF2,S53,3.2,3.2,0.68,11.1,0.422,26.7,11.2,2.38,804,5.41,3.6,1.75,CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\n126,PTBF3,S53,2.7,2.7,0.75,9.1,0.394,78.4,30,2.61,822,5.48,3.59,1.73,CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\n127,PBT-0F,S54,4.5,4.4,0.56,12.2,0.667,61,18.3,3.33,1204,4.9,3.29,1.61,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n128,PBT-1F,S54,5.6,5.4,0.6,14.3,0.657,129,44.1,2.92,1194,4.95,3.29,1.65,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n129,PBT-2F,S54,7.2,7.1,0.74,14.4,0.677,31.8,12.9,2.46,1212,5.15,3.29,1.64,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\n130,PBT-3F,S54,8.6,8.3,0.78,15.2,0.724,76.4,41,1.86,1230,5.2,3.29,1.64,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\n131,PBnDT-HTAZ,S55,4.36,4.3,0.7,11.14,0.552,122.3,47.6,2.57,1032,5.29,2.87,1.98,CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\n132,PBnDT-FTAZ,S55,7.1,6.81,0.79,11.83,0.729,99.6,42.2,2.36,1068,5.36,3.05,2,CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\n133,PBDFDTBT,S56,5.01,5.01,0.78,11.77,0.546,10.1,6.3,1.6,965,5.1,3.5,1.6,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\n134,PBDFDODTBT,S57,4.45,4.45,0.69,9.87,0.653,14,7,2,997,5.11,3.38,1.73,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\n135,PBDFDTBTz,S57,1.24,1.24,0.44,4.92,0.575,18.2,9.6,1.9,835,4.99,3.06,1.93,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\n136,PBDFDTBO,S57,2.88,2.88,0.82,5.04,0.7,32.4,27,1.2,981,5.19,3.49,1.7,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\n137,PBDTT-BT,S58,1.85,1.85,0.88,5.83,0.36,32.6,6.8,4.8,1072,5.26,3.59,1.67,CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\n138,PBDTF-BT,S58,2.88,2.88,0.85,8.41,0.403,22.8,7.6,3,1040,5.24,3.54,1.7,CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\n139,PBDFT-BT,S58,4.42,4.42,0.73,9.94,0.609,11.6,4,2.9,1040,5.08,3.4,1.68,CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\n140,PBDFF-BT,S58,2.6,2.6,0.8,5.84,0.556,13,5.2,2.5,1008,5.11,3.5,1.61,CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\n141,PBDFFBT,S59,3.3,3.3,0.62,9.17,0.584,6.5,5.4,1.2,1095,5.33,3.73,1.6,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\n142,PBDTFBT,S59,4,4,0.72,9.31,0.6,15.2,6.1,2.5,1127,5.3,3.66,1.64,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\n143,PBDTBO,S60,5.7,5.7,0.86,10.4,0.644,254.2,62,4.1,1012,5.27,3.53,1.74,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\n144,PBDTDTBTz,S61,1.7,1.7,0.61,4.5,0.62,18.6,9.3,2,867,5.06,3.11,1.95,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\n145,PBDTTDTBO,S62,5.9,5.9,0.84,11.45,0.613,70.2,41.3,1.7,1113,5.25,3.56,1.69,CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n146,PBDTTDTBT,S62,4.94,4.94,0.75,10.29,0.64,25.1,16.7,1.5,1129,5.15,3.49,1.66,CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n147,PBDTTDTBTz,S62,3.1,3.1,0.54,9.47,0.606,10.5,3.4,3.1,967,4.92,3.14,1.78,CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n148,PBDT?DTBSe,S63,5.18,5.18,0.6,13.58,0.64,42.2,20.1,2.1,1157,5.18,3.63,1.55,CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\n149,PBDT?DTBT,S63,5.01,5.01,0.72,11.16,0.62,46.2,22,2.1,1109,5.26,3.54,1.72,CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\n150,PBDT-T-FBSe,S64,5,5,0.78,11.8,0.54,59.1,27.6,2.14,1419,5.19,3.59,1.6,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\n151,PIDT-T-FBSe,S65,4.84,4.84,0.75,14.07,0.459,57.1,32.6,1.75,1129,5.41,3.85,1.56,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n152,PBPT-12,S65,5.11,5.11,0.75,12.56,0.542,63.9,22.2,2.88,1242,5.44,3.91,1.53,CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\n153,PBDTTBT,S66,5.66,5.66,0.92,10.7,0.575,49.3,27.4,1.8,1128,5.31,3.56,1.75,CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\n154,PBDTP-DTBT,S67,8.07,8.07,0.88,12.94,0.709,64.4,32.2,2,1117,5.35,3.65,1.7,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\n155,PBDTPO-DTBO,S68,6.2,6.2,0.89,11,0.64,27.2,17,1.6,1165,5.56,3.91,1.65,CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\n156,PBDTPO-DTBT,S68,3.4,3.4,0.78,9.3,0.47,25.2,18,1.4,1181,5.46,3.84,1.62,CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\n157,PBDTPO-FBT,S69,2.7,2.7,0.7,7.23,0.471,6.8,3.4,2,1279,5.43,3.9,1.53,CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\n158,PBDTTBO,S70,7.4,7.4,0.86,12.8,0.67,268.8,62.5,4.3,1144,5.46,3.68,1.78,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\n159,PBDTPBO,S70,6.4,6.4,0.85,11.8,0.64,285.1,64.8,4.4,1133,5.4,3.62,1.78,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\n160,PBDTFBO,S70,5.4,5.4,0.81,11.2,0.6,284.8,60.6,4.7,1113,5.38,3.6,1.78,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\n161,PTBFTDTBT,S71,6.42,6.42,0.78,13.51,0.61,142.9,42.7,3.3,1144,5.2,3.57,1.63,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\n162,DTffBT,S72,7.16,7.16,0.9,12.2,0.621,82.1,39.1,2.1,1141,5.53,3.8,1.73,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\n163,DTBT,S72,4.53,4.53,0.78,11.7,0.476,104.8,52.4,2,1105,5.42,3.77,1.65,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\n164,DTfBT,S72,5.22,5.22,0.85,11.5,0.522,74.7,39.3,1.9,1123,5.48,3.81,1.67,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\n165,PTBDTDTBT,S73,3.4,3.4,0.69,8.89,0.554,71.4,27.8,2.57,1225,5.48,3.92,1.56,CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\n166,PTBDTffDTBT,S74,4.8,4.8,0.86,12.17,0.46,34.2,18,1.9,996,5.46,3.72,1.74,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\n167,PTBDTDTBT,S74,1.9,1.9,0.68,6.69,0.42,32.6,19.2,1.7,960,5.29,3.67,1.62,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\n168,PBDT_TEH-DT_H-BTff,S75,4.46,4.46,0.68,11.87,0.552,29,14.5,2,1164,5.33,3.61,1.72,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n169,PBDT_TEH-DT_EH-BTff,S75,6.2,6.2,0.76,13.17,0.619,33.3,22.2,1.5,1164,5.34,3.58,1.76,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\n170,PBDT_TEH-HDO_H-BTff,S75,8.3,8.3,0.78,15.38,0.692,49.5,27.5,1.8,1201,5.31,3.61,1.7,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\n171,PBnDT-FTAZ,S76,6.81,6.81,0.79,11.83,0.729,99.6,42.2,2.36,1068,5.36,3.36,2,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\n172,PFBT-BDT,S77,2.81,2.81,0.94,6.5,0.46,13,6.2,2.1,997,5.44,3.48,1.96,CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\n173,P(BDT-T-BT),S78,3.72,3.72,0.82,9.45,0.48,22.9,10.4,2.2,1028,5.35,3.53,1.82,CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\n174,P(BDT-TT-BT),S78,4.93,4.93,0.69,11.34,0.63,65.6,32.8,2,1477,5.21,3.43,1.78,CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\n175,P(BDT-TT-BO),S79,7.05,7.05,0.76,13.87,0.666,59.1,21.1,2.8,1461,5.31,3.54,1.77,CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\n176,P(BDT-TT-HBT),S80,4.37,4.37,0.72,10.12,0.6,73.9,23.1,3.2,1389,5.29,3.59,1.7,CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\n177,P(BDT-TT-FBT),S80,3.56,3.56,0.81,8,0.55,47.3,16.9,2.8,1425,5.37,3.64,1.73,CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\n178,PBDTT?DTTBT,S81,6.03,6.03,0.78,12.46,0.62,31.1,14.8,2.1,1549,5.11,3.46,1.65,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\n179,PBDTT?DTBT,S81,2.34,2.34,0.82,5.78,0.495,56,20,2.8,1465,5.15,3.52,1.63,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\n180,PBDT?TBT,S82,4.9,4.9,0.96,9.1,0.518,20.5,11.1,1.85,1160,5.27,3.48,1.79,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\n181,PBDT?TTBT,S82,6.3,6.3,0.8,11.83,0.666,16,6.3,2.54,1385,5.09,3.36,1.73,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\n182,PTzBT-10HD,S83,5.2,4.9,0.81,10.2,0.62,60,20,3,1367,5.21,3.41,1.8,CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n183,PTzBT-10OD,S83,3.8,3.6,0.84,8.5,0.54,35,16,2.2,1479,5.2,3.4,1.8,CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n184,PTzBT-12HD,S83,4.8,4.6,0.81,10,0.6,29,24,1.2,1423,5.2,3.4,1.8,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n185,PTzBT-12OD,S83,5.8,5.7,0.82,11.3,0.62,65,41,1.6,1535,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n186,PTzBT-14HD,S83,5.4,5.2,0.82,9.9,0.66,290,33,8.8,1479,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n187,PTzBT-14OD,S83,5.1,4.9,0.82,9.8,0.64,130,44,3,1591,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n188,PTzBT-EHOD,S83,5.8,5.6,0.88,10.3,0.64,1110,43,25,1423,5.21,3.41,1.8,CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n189,PTzBT-BOBO,S83,5.9,5.6,0.89,10.5,0.63,37,16,2.3,1311,5.23,3.43,1.8,CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n190,PTzBT-BOHD,S83,6.7,6.5,0.89,11.4,0.65,110,35,3.1,1423,5.23,3.43,1.8,CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n191,PTzBT-BOOD,S83,4.7,4.4,0.9,8.5,0.62,47,28,1.7,1535,5.23,3.43,1.8,CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n192,PTzBT-14HD,S84,3.1,3,0.92,6.1,0.56,18,13,1.38,1479,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n193,PTzBT-14HD,S84,4.6,4,0.88,7.8,0.67,60,20,3,1479,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n194,PTzBT-14HD,S84,5.7,5.3,0.84,10.6,0.64,300,33,9.09,1479,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n195,PTzBT-14HD,S84,5.3,4.8,0.85,9.2,0.68,1450,73,19.86,1479,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n196,PTzBT-14HD,S84,3.2,3.2,0.92,6.1,0.56,18,13,1.38,1479,5.21,3.41,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\n197,PTzQT-14,S84,1.6,1.6,0.64,6,0.43,27,15,1.8,1283,5.1,3.3,1.8,CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\n198,PTzBT-HD,S84,0.8,0.8,0.96,2.3,0.37,16,8.7,1.84,754,5.3,3.5,1.8,CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\n199,PDPP-BBT,S85,1.51,1.51,0.78,3.73,0.52,9.7,4.7,2.06,872,5.47,3.74,1.7,CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\n200,TDPP-BBT,S85,2.78,2.78,0.74,6.72,0.56,19,11.6,1.64,884,5.15,3.69,1.43,CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\n201,PBTPyDPP,S86,4.88,4.88,0.92,7.96,0.658,22,18,1.22,1043,5.77,3.86,1.71,CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\n202,PDPP3T,S87,7.1,6.9,0.67,15.4,0.69,400,147,2.72,859,5.3,3.74,1.33,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\n203,PDPPTPT,S87,7.4,7.3,0.8,14,0.67,143,72,1.98,853,5.48,3.66,1.53,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\n204,PDPP3TaltTPT,S87,8,7.8,0.75,15.9,0.67,154,42,3.68,1681,5.16,3.73,1.43,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\n205,C3-DPPTTT,S88,8.8,8.8,0.57,23.5,0.66,154,80,1.9,1139,5.08,3.69,1.39,O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\n206,C3-DPPTTSe,S88,7.6,7.6,0.56,21.5,0.63,238,95,2.5,1187,5.07,3.7,1.37,O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\n207,C3-DPPTTTe,S88,7.1,7.1,0.52,21.7,0.63,272,91,3,1237,5.05,3.73,1.32,O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\n208,PDPP2FT-C12,S89,5.2,4.8,0.65,12.2,0.6,78,46,1.7,714,5.2,3.8,1.4,CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\n209,PDPP2FT-C14,S89,6.5,6.2,0.65,14.8,0.64,92,58,1.59,771,5.2,3.8,1.4,CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\n210,PDPP2FT-C16,S89,6.2,5.7,0.65,12.3,0.69,87,55,1.6,827,5.3,3.9,1.4,CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\n211,PBDTT-FDPP,S90,4.7,4.5,0.77,10.9,0.56,77.4,35.2,2.2,1209,5.26,3.64,1.51,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\n212,PBDTT-DPP,S90,6.5,6.4,0.73,13.7,0.65,88.7,40.3,2.2,1241,5.3,3.63,1.46,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\n213,PBDTT-SeDPP,S90,7.2,7,0.69,16.8,0.62,79.8,38,2.1,1336,5.25,3.7,1.38,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\n214,PDPP2TBP,S91,5.7,5.7,0.8,11.5,0.63,176.9,49,3.61,1041,5.39,3.76,1.63,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\n215,F1-PDPP2TBP,S91,3.7,3.7,0.89,6.7,0.62,277.8,67.6,4.11,1077,5.44,3.85,1.59,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\n216,F2-PDPP2TBP,S91,4.1,4.1,0.93,7.7,0.56,142.6,72,1.98,1077,5.48,3.78,1.7,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\n217,PDPPTNT,S92,4.7,4.7,0.76,11.8,0.52,91.3,63.8,1.43,1015,5.29,3.79,1.5,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\n218,DT-PDPPTPT,S93,3.2,3.2,0.81,6.6,0.59,215.6,89.2,2.42,1077,5.4,3.86,1.54,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n219,DT-PDPP3T,S93,4.8,4.8,0.65,10.6,0.71,457.5,136.8,3.34,1083,5.25,3.89,1.36,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n220,DT-PDPP2T-DBT,S93,5.3,5.3,0.76,10.2,0.68,552,149.9,3.68,1183,5.36,3.74,1.62,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n221,DT-PDPP4T,S93,7.1,7.1,0.64,16,0.69,640.5,218.5,2.93,1165,5.09,3.66,1.43,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n222,reg-PDPP/TPDalt2T,S94,5.3,5.1,0.78,9.6,0.68,137,50,2.74,1330,5.78,3.84,1.42,CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\n223,DTS-D-C,S95,0.77,0.77,0.88,1.9,0.46,21.9,15.9,1.38,1133,5.3,3.94,1.44,CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\n224,DTS-Ch,S95,1.44,1.44,0.95,5.83,0.26,13.3,8.3,1.6,764,5.4,3.72,1.68,CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\n225,DTS-Chy,S95,1.36,1.36,0.85,3.91,0.41,10.7,6.3,1.7,776,5.27,3.7,1.57,CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\n226,DTS-T-Ch,S95,5.17,5.17,0.8,10.1,0.64,23.4,11.7,2,928,5.16,3.43,1.73,O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\n227,DTS-T-Chy,S95,3.79,3.79,0.68,9.1,0.61,19.8,7.9,2.5,940,5.02,3.46,1.56,O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\n228,DTS-T6,S95,2.7,2.7,0.98,6.01,0.46,27.9,19.1,1.46,832,5.21,3.49,1.72,CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\n229,BDT-C6,S95,0.45,0.45,0.83,1.81,0.3,44.3,18.6,2.38,854,5.23,3.37,1.86,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\n230,BDT-T6,S95,0.73,0.73,0.87,2.64,0.33,66.4,18.8,3.53,860,5.32,3.4,1.92,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\n231,DTS-C4,S95,4.28,4.28,0.91,10.1,0.47,83,41.5,2,770,5.33,3.7,1.63,CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\n232,DTS-Ceh,S95,5.15,5.15,0.94,9.46,0.58,90.8,53.4,1.7,882,5.27,3.65,1.62,CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\n233,DTS-C8,S95,2.35,2.35,0.88,5,0.53,92.6,46.3,2,882,5.27,3.63,1.64,CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\n234,DTS-C6,S95,7.85,7.85,0.86,14.39,0.64,72.8,42.8,1.7,826,5.25,3.63,1.62,CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\n235,BTI-BDT,S96,4.39,4.39,0.88,9.69,0.518,71.5,21.8,3.28,875,5.41,2.3,1.93,CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\n236,BTI-BDT(2),S96,5.5,5.5,0.92,9.62,0.62,100.3,34,2.95,1044,5.39,2.54,1.93,CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\n237,�s�s1,S97,0.6,0.6,0.56,2.83,0.38,32,18.8,1.7,1385,5.35,3.94,1.41,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\6=O)=O)=C4)S3)=N8)=C8S2)S1\n238,TT2,S97,3.4,3.4,0.58,8.54,0.69,127,36.3,3.5,1885,5.43,3.98,1.45,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\n239,BT1,S97,3.29,3.29,0.73,6.72,0.67,142,67.6,2.1,1435,5.5,3.98,1.52,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\n240,BT2,S97,4.18,4.18,0.62,10.07,0.67,231,59.2,3.9,1935,5.41,3.92,1.49,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\n241,IP1,S98,0.51,0.51,0.39,3.26,0.4,88.3,40.1,2.2,970,4.9,3.8,1.1,O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\n242,IP2,S98,0.27,0.27,0.3,1.73,0.52,14.9,8.8,1.7,926,4.8,3.8,1,O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\n243,IP3,S98,1.3,1.3,0.73,3.22,0.53,23.9,10.4,2.3,915,5.4,3.8,1.6,O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\n244,IsoC6,S99,5.2,5.1,0.69,12.3,0.58,207,80,2.6,1153,5.58,3.93,1.57,CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\n245,IsoC8,S99,5.6,5.2,0.7,12.7,0.57,146,70,2.1,1209,5.58,3.9,1.57,CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\n246,IsoC10,S99,4.2,4.1,0.63,11.6,0.54,126,61,2.1,1265,5.6,4.06,1.55,CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\n247,IsoC12,S99,4.1,4,0.66,11.3,0.52,125,65,1.9,1321,5.55,3.84,1.58,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\n248,IsoC12,S99,4.1,4,0.69,11,0.51,103,41,2.5,1321,5.55,3.89,1.58,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\n249,Iso2EH,S99,0.3,0.3,0.88,0.8,0.58,126,53,2.4,1209,5.81,3.93,1.6,CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\n250,PNDTI-T,S100,1.23,1.2,0.56,4.8,0.46,26.1,13.8,1.9,1161,5.8,4,1.4,O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\n251,PNDTI-TT,S100,2.07,2,0.62,6.4,0.5,48.9,19,2.6,1217,5.7,4.1,1.3,O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\n252,PNDTI-DTT,S100,3.28,3.2,0.66,9.6,0.51,68.5,28.7,2.4,1273,5.6,4,1.3,O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\n253,PNDTI-BT,S100,2.6,2.6,0.66,8.1,0.49,90.4,27.4,3.3,1243,5.6,4.1,1.3,O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\n254,PBDTT-TT,S101,7.42,7.35,0.77,14.99,0.639,132.1,95,1.39,918,5.3,3.17,1.58,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n255,PBDTT-O-TT,S101,7.1,7.01,0.73,15.17,0.644,118.6,78,1.52,950,5.18,3.15,1.53,CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\n256,PBDTT-S-TT,S101,8.42,8.35,0.84,15.32,0.655,172.3,118,1.46,982,5.41,3.27,1.57,CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\n257,PBDT-TS1,S102,9.48,9.19,0.8,17.37,0.661,64.9,29.4,2.21,982,5.33,3.52,1.51,CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\n258,PBTz4T,S103,2.6,2.6,0.74,5.6,0.63,114,36.1,3.2,1053,5.07,3.53,1.65,CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\n259,PNNT12HD,S104,8.2,8,0.82,15.6,0.64,88.9,36,2.47,1459,5.22,3.54,1.68,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\n260,PNNT12DT,S104,4.1,4,0.86,7.3,0.65,139,46.1,3.02,1683,5.22,3.54,1.69,CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\n261,PNNTDT,S104,5.5,5.2,0.83,12.3,0.54,310,31,10,1347,5.25,3.54,1.64,CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\n262,PNDT3BTz-DT,S105,3.8,3.8,0.7,8.4,0.64,54.5,30.3,1.8,1239,5.15,3.45,1.7,CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\n263,PNDT3NTz-DT,S105,4.9,4.9,0.83,11.3,0.52,310,31,10,1347,5.25,3.65,1.6,CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\n264,PNTz4TF2,S106,10.5,10.1,0.82,19.3,0.67,1520,66.5,22.9,1309,5.38,3.53,1.6,CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\n265,PNTz4TF4,S106,6.5,5.9,0.93,10.5,0.66,34.1,15.8,2.16,1345,5.49,3.56,1.62,CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\n266,PBDT-DTBT,S107,2.11,2.11,1,5.8,0.346,130,40.5,3.2,1409,5.26,3.1,1.73,CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\n267,PBDT-DTNT,S107,6,6,0.8,11.71,0.61,59.3,24.1,2.46,1517,5.19,3.26,1.58,CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\n268,PTzNTz-EHBO,S108,9,8.7,0.84,16,0.67,64.3,32.7,2,1301,5.41,3.45,1.58,CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\n269,PTzNTz-EHHD,S108,8.8,8.5,0.84,15.6,0.67,91.8,47,2,1413,5.4,3.46,1.58,CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\n270,PTzNTz-BOBO,S108,8.8,8.5,0.84,16.6,0.63,113.2,51.6,2.2,1413,5.4,3.46,1.57,CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\n271,PTzNTz-BOHD,S108,5.2,4.8,0.84,9.8,0.63,59.2,29.1,2.2,1525,5.41,3.44,1.57,CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\n272,PF-C12NT,S109,6.51,6.51,0.87,12.19,0.614,69.3,23.4,2.95,1325,5.47,3.79,1.68,CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\n273,PAF-C12NT,S109,3.64,3.64,0.69,8.45,0.625,59.9,16.6,3.6,1505,5.4,3.85,1.55,CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\n274,PCz-C12NT,S109,4.85,4.85,0.76,11.31,0.564,84.3,21.6,3.89,1340,5.35,3.72,1.63,CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\n275,PBDT-C12NT,S109,5,5,0.68,10.74,0.685,69.4,22.3,3.1,1849,5.19,3.68,1.51,CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\n276,PN1,S110,2.78,2.78,0.85,8.65,0.378,32.7,14.2,2.3,1257,5.39,3.75,1.64,CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\n277,PIDT-EHNT,S111,1.49,1.34,0.86,4.33,0.4,42.1,19.4,2.17,1677,5.48,3.79,1.69,CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\n278,PIDT-DTNT,S111,2.97,2.52,0.8,8.26,0.45,35.6,17.6,2.02,1621,5.48,3.83,1.65,CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\n279,PIDT-C12NT,S111,5.05,4.88,0.9,10.21,0.55,43.6,17.5,2.49,1953,5.52,3.88,1.64,CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\n280,NT812,S112,10.33,10.18,0.72,19.09,0.729,118.9,56.6,2.1,1135,5.29,3.4,1.4,CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\n281,NT1014,S112,3.03,2.93,0.77,7.25,0.529,165.5,59.1,2.8,1247,5.29,3.4,1.4,CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\n282,P��NDTDTNT,S113,8.01,8.01,0.8,15.55,0.644,86.4,67.3,1.3,1459,5.4,3.64,1.58,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\n283,P��NDTDTNT,S113,3.6,3.6,0.8,8.41,0.535,60.5,28.3,2.1,1459,5.46,3.64,1.65,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\n284,poly(CR-TPA),S114,2.15,2.15,0.79,6.87,0.4,15.6,9.8,1.6,611,5.55,2.6,1.8,CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\n285,poly(NTD-TPA),S114,1.52,1.52,0.76,6.02,0.33,8.2,5.9,1.5,627,5.4,3.37,2.03,CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\n286,BTT-TP,S115,0.35,0.35,0.993,0.764,0.468,16.4,10.3,1.59,1372,5.6,3.85,1.75,CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\n287,BTT-FT,S115,1.01,1.01,0.919,2.04,0.54,24.8,20,1.24,1407,5.52,3.74,1.78,CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\n288,BTT-NTz,S115,2.73,2.73,0.755,5.98,0.605,62.7,39.9,1.57,2091,5.41,3.73,1.68,CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\n289,PDCBT,S116,7.2,7,0.91,11,0.72,40.2,24.8,1.62,782,4.9,3,1.9,CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\n290,rr-PTB7-Th,S117,7.04,6.96,0.78,15.35,0.583,89.1,35.8,2.49,1807,5.2,3.68,1.61,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\n291,rr-PTBS,S117,10.31,10.19,0.82,19.63,0.633,103,40.7,2.53,1871,5.22,3.84,1.58,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\n292,P3TI,S118,6.3,6.3,0.7,13.1,0.69,211.7,73,2.9,1209,5.82,3.83,1.5,CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\n293,O-PBDT,S119,1.56,1.56,0.83,4.18,0.45,32.3,10.9,2.96,474,5.31,2.94,2.21,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\n294,SO-PBDT,S119,1.73,1.73,0.91,4.4,0.43,27.7,9.3,2.98,950,5.36,3.11,2.03,CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\n295,S-PBDT,S119,4,4,0.99,7.66,0.53,61.3,16.1,3.81,506,5.41,3.26,2.07,CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\n296,PBDTT,S120,6.12,6.12,0.93,11.95,0.55,49.7,18.7,2.7,606,5.44,3.46,2.13,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\n297,P3HDTTT,S121,3.4,3.4,0.82,6.33,0.66,18.9,10.5,1.8,500,5.3,3.4,1.9,CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\n298,PT-C1,S122,1.69,1.69,0.81,5.31,0.392,6.9,4.3,1.62,350,5.15,2.96,1.92,CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\n299,PT-C2,S122,2.14,2.14,0.81,5.44,0.484,5.6,3.2,1.75,432,5.11,2.95,1.89,CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\n300,PT-C3,S122,3.25,3.25,0.77,7.22,0.584,113.4,69.4,1.63,544,5.1,2.98,1.91,CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\n301,P3HST,S123,0.34,0.34,0.63,1.27,0.34,28.5,15,1.9,228,4.9,3.08,1.82,CC1=CC(SCCCCCC)=C(C)S1\n302,P3HST-co-Th,S123,0.5,0.5,0.63,2.32,0.34,81.9,39,2.1,310,5.02,3.19,1.83,CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\n303,C6-TT,S124,0.6,0.6,0.75,2.5,0.34,42,20,2.1,444,5.25,3.05,1.9,CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\n304,PBTDN,S125,3.2,3.2,0.83,9.2,0.41,9.9,7.7,1.29,658,5.12,2.9,2.22,CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\n305,PBTADN,S125,3.4,3.4,0.89,7.4,0.514,65.4,44.8,1.46,683,5.36,3.34,2.02,CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\n306,POPT,S126,1.71,1.71,0.56,5.16,0.6,17.6,16,1.1,300,5.34,3.58,1.76,CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\n307,POPTT,S126,1.73,1.73,0.63,6.83,0.4,19.6,14,1.4,464,5.43,3.5,1.93,CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\n308,POPQT,S126,3.44,3.44,0.71,8.67,0.56,9.3,6.2,1.5,546,5.49,3.52,1.97,CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\n309,P1,S127,2.85,2.85,0.62,6.92,0.66,17,9.7,1.75,556,5.22,3.21,2.01,CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\n310,P2,S127,3.44,3.44,0.64,9.3,0.58,150,44,3.4,664,5.22,3.26,1.96,CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\n311,P3,S127,4.49,4.49,0.73,11.49,0.53,23,16,1.44,689,5.37,3.47,1.9,CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\n312,PBDT-3MT,S128,4.52,4.52,0.86,10.5,0.5,92,26.4,3.9,614,5.43,3.36,2.07,CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\n313,PBDT-BT,S129,2.2,2.01,0.82,5.86,0.458,28.7,14.9,1.93,975,5.37,3.25,2.1,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\n314,PBDT-BTC,S129,0.55,0.52,0.98,1.27,0.414,39.8,11.8,3.37,1025,5.58,3.53,1.96,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\n315,PBDT-BTCox,S129,5.06,4.9,0.86,10.1,0.584,66.5,37.6,1.77,1057,5.5,3.51,1.74,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\n316,PBDT[2F]T,S130,7,6.8,0.9,10.7,0.72,25.8,12.6,2,592,5.05,2.95,2.1,CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\n317,PBDT[2H]T,S130,2.9,2.8,0.8,6.3,0.58,33.2,15.5,2.1,556,5.32,3.24,2.1,CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\n318,PBTTPD,S131,4.7,4.7,0.95,8.02,0.62,13.6,9.7,1.4,793,5.56,3.1,1.82,CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\n319,PDTTTPD,S132,5.1,5.1,0.85,8.99,0.67,11,9.2,1.2,931,5.54,3,1.84,CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\n320,PBTTPD,S133,1.9,1.9,0.9,5.01,0.42,103,50,2,920,5.66,3.86,1.8,CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\n321,PTTTPD,S133,6.1,5.53,0.92,10.51,0.63,95,41,2.3,1002,5.66,3.86,1.8,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\n322,PTTTPD-C8C8 (P1),S134,4.96,4.84,0.87,9.5,0.6,110,44,2.5,1002,5.66,3.86,1.81,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\n323,PTTTPD-C8 (P2),S134,3.2,2.92,0.81,6.7,0.59,52,27,1.9,875,5.56,3.73,1.87,CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\n324,PTTTPD-EG (P3),S134,2.09,1.99,0.76,4.91,0.56,20,11,1.8,851,5.31,3.54,1.8,CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\n325,PTTSPD-C8C8 (P4),S134,5.11,5.01,0.88,8.8,0.66,81,42,1.9,1050,5.57,3.69,1.79,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\n326,PTTFPD-C8C8 (P5),S134,0.5,0.43,0.81,1.57,0.39,55,20,2.7,986,5.65,3.8,1.93,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\n327,PTTFPD-C8 (P6),S134,3.4,3.26,0.8,6.76,0.63,70,41,1.7,860,5.54,3.75,1.87,CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\n328,PTSTPD-C8C8 (P7),S134,4.37,4.28,0.88,8.14,0.61,71,36,2,1050,5.49,3.82,1.78,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\n329,PTSTPD-C8C8 (P8),S134,4.59,4.41,0.87,7.75,0.68,85,41,2.1,1098,5.48,3.69,1.76,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\n330,PSBTSPD-C8 (P9),S134,7.13,7.03,0.85,13.17,0.64,45,29,1.6,757,5.55,3.82,1.68,CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\n331,P(PTQD-Th),S135,5.54,5.48,0.92,10.76,0.56,37.2,19.4,1.92,701,5.73,3.76,1.84,CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\n332,P(PTQD-2Th),S135,5.67,5.58,0.8,11.82,0.6,38.9,18.5,2.1,783,5.54,3.8,1.7,CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\n333,PPDT1,S136,3.28,3.28,0.87,8.3,0.453,89.3,49.6,1.8,847,5.27,2.68,2,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\n334,PPDT2,S136,4.08,4.08,0.85,9.26,0.521,75.2,41.8,1.8,843,5.47,2.68,1.97,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\n335,PPDT3,S136,5.33,5.33,0.89,8.5,0.706,55.1,32.4,1.7,979,5.36,2.83,1.9,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\n336,PPDT4,S136,0.95,0.95,0.86,3.5,0.316,45.6,30.4,1.5,735,5.59,2.77,2.03,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\n337,PPDT5,S136,2.57,2.57,0.75,8.47,0.405,30.5,12.7,2.4,819,5.39,2.87,1.82,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\n338,PSOxTT,S137,2.27,2.1,0.56,7.5,0.49,48.6,24.3,2,1006,5,3.27,1.73,CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\n339,PSOTT,S137,4.18,4.1,0.62,10.2,0.65,35.7,15.5,2.3,974,5.1,3.31,1.79,CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\n340,PSEHTT,S137,5.06,5,0.65,12.6,0.61,133.6,33.9,3.94,974,5.1,3.3,1.82,CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\n341,PBDT-BDTP (P1),S138,5.05,5.05,0.89,10.37,0.547,156.8,49,3.2,1445,5.53,2.68,1.98,O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\n342,PS-BDTP (P2),S138,6.76,6.76,0.91,9.96,0.745,180.1,62.1,2.9,1131,5.51,2.8,1.8,O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\n343,PDTPO-BDTO,S139,6.84,6.84,0.93,10.4,0.706,291.1,97.7,2.98,960,5.38,3.37,2.02,CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\n344,PDTPO-BDTT,S139,6.84,6.84,0.96,10.1,0.705,188.5,75.4,2.5,1092,5.44,3.55,1.98,CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\n345,PThBDTP,S140,9.13,8.98,0.96,12.59,0.755,264,89.8,2.94,1083,5.52,2.74,1.86,O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\n346,PFTTz,S141,2.64,2.64,0.91,7.2,0.4,93.6,36,2.6,613,5.58,3.55,2.17,CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\n347,PCTTz,S141,0.71,0.71,0.76,2.27,0.41,111.8,43,2.6,628,5.46,3.56,2.11,CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\n348,PBTTz,S141,1.41,1.41,0.52,4.64,0.58,12,10,1.2,725,5.24,3.57,1.73,CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\n349,PIFTBT6,S142,0.97,0.97,0.98,3.25,0.31,63.5,26.3,2.42,916,5.49,3.46,1.97,CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\n350,PIFTBT10,S142,2.44,2.44,1,6.1,0.4,21,7.8,2.65,1141,5.45,3.36,2,CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\n351,PIFDTQ10,S142,3.04,3.04,1,7.57,0.4,45.9,22.5,2.03,1289,5.47,3.44,1.97,CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\n352,P3FTBT6,S142,4.5,4.5,1.04,10.3,0.42,24.9,14.2,1.75,1249,5.45,3.45,1.96,CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\n353,PITBT,S143,5.92,5.92,0.94,12.51,0.502,25.6,12.6,2.03,640,5.48,3.66,1.82,CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\n354,PITFBT,S143,9.14,9.14,0.9,15.36,0.659,43.6,27.8,1.57,658,5.5,3.68,1.8,CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\n355,HXS-1,S144,5.4,5.4,0.81,9.8,0.69,51.4,16.6,3.1,861,5.21,3.35,1.95,CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\n356,PCDTTPD,S145,1.82,1.82,1.07,4.72,0.36,24,13,1.8,860,5.71,3.74,2.05,CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\n357,PCDTTPD-ic,S145,0.14,0.14,1.01,0.56,0.25,24,18,1.3,1085,5.47,3.39,2.21,CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\n358,PCDTTPD-C6C8,S145,0.13,0.13,1,0.35,0.39,10,6,1.7,973,5.5,3.5,2.06,CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\n359,PCTTPD,S146,1.14,1.14,0.94,2.7,0.45,36.2,20,1.81,973,5.72,3.69,2.03,CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\n360,PCTTTPD,S146,1.25,1.25,0.9,3.86,0.36,40.9,12.5,3.27,1085,5.67,3.65,2.02,CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\n361,PCBTTPD,S146,3.42,3.42,0.86,7.79,0.51,65.2,20.2,3.23,1137,5.57,3.66,1.91,CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\n362,PTTDBC-PhQC8,S147,2.63,2.63,0.88,7.13,0.42,8.6,5.5,1.56,1308,5.31,3.42,1.89,CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\n363,PTTDBC-BTC12,S147,4.5,4.5,0.93,8.78,0.55,29.1,14.6,2,1274,5.35,3.41,1.94,CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\n364,PC1,S148,2.45,2.45,0.88,5.77,0.441,16.8,13.8,1.2,1118,5.41,3.67,1.9,CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\n365,PC2,S148,7.26,7.26,0.94,12.84,0.587,44.8,23.3,1.9,1178,5.43,3.56,2.01,CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\n366,PC3,S148,6.68,6.68,0.93,11.18,0.633,23.1,14.7,1.6,1262,5.44,3.65,1.97,CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\n367,HD-PDFC-DTBT,S149,7.39,7.39,0.93,14.11,0.563,98.1,38.3,2.56,1010,5.32,3.3,1.96,CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\n368,PAn-BTBT (P1),S150,2.23,2.23,0.96,4.4,0.53,185,57,3.24,1425,5.4,3.28,2.12,CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\n369,PAn-BTBT (P2),S150,1.42,1.42,0.89,3,0.53,152,75,2.03,1571,5.3,3.19,2.11,CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\n370,PTP27-DBT,S151,3.5,3.5,0.82,10.2,0.41,14,7,2,1129,5.4,2.91,1.85,CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\n371,PTP36-DBT,S151,0.9,0.9,0.79,4.4,0.268,14,7,2,1129,5.7,3.18,1.85,CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\n372,PPhIBDT-C12 (P2),S152,1.5,1.46,0.8,3.43,0.547,28.9,8.5,3.4,1008,5.36,3.02,2.1,CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\n373,PPhIBDT-ThEH (P3),S152,3.7,3.65,0.89,7.01,0.586,43.4,15.5,2.8,1027,5.57,3.07,2.07,CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\n374,PBEHTT,S153,2.05,2.03,0.71,5.85,0.49,48.9,25.9,1.89,963,5.42,3.22,2.22,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\n375,PTTEHV,S153,1.19,1.03,0.53,5.02,0.39,4.2,2.5,1.65,584,5.4,3.53,1.8,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\n376,PCEHTT,S153,0.87,0.86,0.69,5,0.25,4.5,2.8,1.62,962,5.32,3.44,1.84,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\n377,PBTOTT,S153,1.03,0.99,0.75,5.3,0.25,284.6,103,2.76,946,5.16,3.34,1.82,CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\n378,PCPEHTT,S153,2.41,2.4,0.73,9.68,0.34,11.7,8,1.46,958,5.01,3.3,1.85,CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\n379,PBTOxTT,S153,0.94,0.91,0.53,5.54,0.31,150.8,56.6,2.66,978,4.91,2.77,1.8,CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\n380,PPEHTT,S153,0.82,0.8,0.5,4.41,0.36,13.5,8.4,1.6,959,4.91,3.18,1.73,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\n381,PDEHTT,S153,5.71,5.6,0.74,10.8,0.7,44.5,19.7,2.26,1115,5.65,3.68,1.97,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\n382,POAPPO-BDT (Pa),S154,4.54,4.54,0.92,8.19,0.602,76.1,31.7,2.4,1321,5.41,3.28,2.13,CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\n383,POAPPO-BDT (Pb),S154,0.46,0.46,0.66,1.51,0.462,52.3,24.9,2.1,1321,5.34,3.15,2.19,CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\n384,POAPPO-BDT (Pc),S154,2.15,2.15,0.66,5.46,0.596,45.2,22.6,2,1321,5.3,3.09,2.21,CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\n385,PBDTTPD,S155,7.1,7.1,0.93,10.89,0.7,48,20,2.4,737,5.56,3.75,1.8,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\n386,PNDTTPD (P1),S156,4,4,0.69,11.54,0.5,90,30,3,914,5.3,3.5,1.8,O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\n387,PBDTTPD (P2),S156,3.4,3.4,0.78,8.37,0.52,170,70,2.4,864,5.47,3.59,1.88,O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\n388,PBDTTPD,S157,4.2,4.2,0.87,9.1,0.538,75.9,33,2.3,737,5.43,3.4,1.82,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\n389,PBDTT-LTPD,S158,7.59,7.59,1,14.32,0.52,36.2,15.6,2.32,1383,5.62,3.43,2.04,CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\n390,PTAC-TPD (P1),S159,4.8,4.8,0.89,8.1,0.67,113.5,20.5,5.53,1574,5.35,3.51,1.9,CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\n391,PBDT(F)TPD,S160,3,2.7,0.9,7.8,0.42,34.8,14.5,2.4,837,4.85,2.76,1.78,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\n392,PBDT(T)TPD,S160,6.5,6.1,1,11.1,0.58,51.4,16.4,3.1,869,5.01,2.76,1.88,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\n393,PBDT(S)TPD,S160,4.7,4.3,0.98,8.7,0.48,40.1,12.7,3.2,965,4.98,2.76,1.85,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\n394,PBDT-TZNT (P1),S161,3.35,3.35,0.88,7.42,0.51,122.3,48.9,2.5,1315,5.21,3.31,1.9,CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\n395,PBDT-TZNT (P2),S161,7.11,7.11,0.92,11.71,0.65,116.2,74.5,1.56,1539,5.23,3.3,1.93,CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\n396,PBDT-TZNT (P3),S161,1.5,1.5,0.84,3.59,0.49,101.1,53.8,1.88,1539,5.21,3.31,1.9,CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\n397,PBDTFBZO,S162,6.25,6.25,0.91,11.81,0.582,106.3,48.3,2.2,1036,5.38,3.28,1.83,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\n398,PBDTFBZS,S162,7.74,7.74,0.88,12.36,0.712,75.2,39.6,1.9,1068,5.32,3.26,1.81,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\n399,FTAZ,S163,5.75,5.75,0.85,8.89,0.759,149,81,1.84,1068,5.45,3.45,2,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\n400,PrzTAZ,S163,4.75,4.75,0.96,8.33,0.597,78.4,53,1.48,1034,5.66,3.73,1.93,CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\n401,PBnDT?PyCNTAZ,S163,7.52,7.52,0.965,10.92,0.714,200.9,82,2.45,1058,5.67,3.83,1.84,CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\n402,CNTAZ,S163,5.53,5.53,1.03,8.97,0.599,173.3,75,2.31,1082,5.73,3.96,1.77,CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\n403,PTFBDT-BZS,S164,8.24,8.24,0.89,12.67,0.73,223.6,66.8,3.35,1333,5.5,3.69,1.81,CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\n404,PTFBDT-BZO,S164,5.67,5.67,0.96,9.24,0.64,255.1,67,3.81,1317,5.62,3.8,1.82,CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\n405,PTZBIBDT,S165,8.63,8.63,0.87,13.5,0.74,56.7,22.5,2.52,1180,5.34,3.46,1.81,CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\n406,PV-BDTC1,S166,3.25,3.15,0.93,5.9,0.594,91.9,31.7,2.9,1251,5.56,3.49,2.07,CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\n407,PV-BDTC2,S166,7.49,7.33,1.03,10.37,0.7,59.8,35.2,1.7,1383,5.67,3.58,2.09,CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\n408,PBDTBDD (PM6),S167,9.2,9.2,0.98,12.7,0.74,38.6,19.3,2,1248,5.45,3.65,1.8,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\n409,PBDT-HBTA,S168,2.43,2.43,0.58,7.41,0.565,81.1,31.2,2.6,1224,5.13,3.16,1.88,CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\n410,PBDT-FBTA,S168,6,6,0.75,11.9,0.672,43.2,32,1.35,1260,5.26,3.08,1.91,CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\n411,PBDT(O)-T1,S169,4.01,4,0.83,9.6,0.495,52.3,27.5,1.9,1244,5.31,3.45,1.74,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\n412,PBDT(S)-T1,S169,7.48,7.3,0.9,12.3,0.711,66.5,23.8,2.8,1276,5.52,3.56,1.81,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\n413,PBDT(Se)-T1,S169,8.52,8.4,0.92,13.1,0.721,82.4,39.2,2.1,1372,5.53,3.59,1.8,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\n414,PBDT(S)-T1,S170,7.4,7.4,0.89,12.3,0.676,77.5,48.4,1.6,1276,5.52,3.56,1.8,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\n415,POBDT(S)-T1,S170,9.2,9.2,0.98,12.9,0.722,66.5,23.8,2.8,1336,5.65,3.55,1.81,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\n416,PBDT-O1,S171,5.2,5.2,0.87,9.4,0.64,22,20,1.1,1196,5.51,3.52,1.82,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\n417,PBDT-ST1,S171,9,9,0.91,13.7,0.747,34.2,19,1.8,1212,5.53,3.57,1.81,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\n418,PBDT-Se1,S171,8.3,8.3,0.86,13.1,0.747,27.3,17.1,1.6,1260,5.46,3.53,1.8,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\n419,PDBT-T1,S172,9.74,9.74,0.92,14.11,0.75,342,195.4,1.75,1324,5.4,3.4,1.85,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\n420,PBT1-MP,S173,8.7,8.7,0.98,12.9,0.725,24.1,13.4,1.8,1388,5.49,3.46,1.86,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\n421,PBT1-EH,S173,10.3,10.3,0.97,14.21,0.75,25.8,15.2,1.7,1388,5.43,3.43,1.84,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\n422,PBT1-BO,S173,8.1,8.1,0.93,13.03,0.675,35.7,16.2,2.2,1388,5.4,3.41,1.81,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\n423,PIDT-SO,S174,2.31,2.31,0.97,6.96,0.34,133.2,72,1.85,1149,5.4,3.03,2.27,CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\n424,PIDT-DHTSO,S174,3.81,3.81,0.95,8.2,0.48,73.1,45.4,1.61,1481,5.33,3.05,2.2,CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\n425,PBDT-TPTI (P1),S175,5.3,5.3,0.9,9.26,0.636,124.7,30.2,4.13,1245,5.45,2.68,2.03,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\n426,PSB-TPTI (P3),S175,3.64,3.64,0.87,7.62,0.549,21.5,12.2,1.76,1217,5.33,2.72,1.85,CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\n427,PSB-TPTI (P4),S175,3.48,3.48,0.8,10.31,0.422,20.5,11.8,1.74,992,5.34,2.69,1.86,CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\n428,PBDTTTP,S176,5.53,5.53,0.98,8.12,0.695,277.2,69.3,4,1469,5.43,2.6,2.11,O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\n429,PSBT,S177,5.18,5.18,0.94,11.11,0.496,9.9,7.6,1.3,1375,5.4,3.59,1.81,CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\n430,PSBO,S177,3.29,3.29,0.96,8.6,0.401,13.9,7.7,1.8,1415,5.48,3.66,1.82,CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\n431,PSDTBT,S177,3.52,3.52,0.9,9.5,0.413,9,5.3,1.7,1651,5.38,3.56,1.82,CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\n432,PThTITI,S178,5.53,5.53,0.96,8.28,0.698,289.4,106.4,2.72,1045,5.57,2.6,2,CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\n433,PSeTITI,S178,6.17,6.17,0.94,9.35,0.705,318.8,88.8,3.59,1093,5.54,2.78,1.93,CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\n434,PThTD1,S179,6.02,5.86,0.87,9.67,0.716,335.8,58.1,5.78,1057,5.36,2.56,1.82,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\n435,PThTD2,S179,6.9,6.65,0.85,11.95,0.68,146.4,33.2,4.41,944,5.3,2.63,1.82,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\n436,PSeTD1,S179,6.22,5.96,0.83,10.92,0.687,253.5,70.8,3.58,1105,5.34,2.7,1.75,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\n437,PSeTD2,S179,8.18,7.95,0.85,13.55,0.711,93.4,35.5,2.63,992,5.31,2.74,1.75,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\n438,PzNDTT-TPD1,S180,7.5,7.5,0.86,12.73,0.68,56.8,24.9,2.28,1532,5.55,3.52,1.94,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\n439,PzNDTT-TPD2,S180,3.68,3.68,0.88,6.09,0.69,32,24.6,1.3,1532,5.58,3.48,1.98,CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\n440,PDTPO-IDTT,S181,5.47,5.4,0.94,9.14,0.64,41.8,23.9,1.75,1420,5.31,3.27,2.04,CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\n441,PDTPO-IDT,S181,7.33,7.17,0.97,10.55,0.71,68.9,30.2,2.28,1532,5.32,3.27,2.05,CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\n442,PIDT-OHBPz,S182,3.75,3.75,0.83,8,0.566,105.2,70.1,1.5,1437,5.27,3.31,1.69,CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\n443,PIDT-OFBPz,S182,5.13,5.13,0.97,8.96,0.59,156.9,104.6,1.5,1473,5.45,3.56,1.75,CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\n444,PIDT-OBPQ,S182,3.93,3.93,0.86,8.97,0.509,117,78,1.5,1438,5.3,3.58,1.56,CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\n445,P-PDT-IID12OD,S183,5.06,4.46,0.8,9.99,0.63,37.3,26.8,1.39,1639,5.45,3.85,1.6,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\n446,P-PDT-IID12DT,S183,3.1,2.26,0.82,6.63,0.57,20.5,13.5,1.52,1751,5.45,3.85,1.6,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\n447,P-PDT-IIDBOBO,S183,5.28,5.18,0.82,10.7,0.6,106.1,56.9,1.87,1415,5.5,3.81,1.69,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\n448,P-PDT-IIDHDHD,S183,1.09,0.94,0.9,2.05,0.59,28.7,19,1.51,1639,5.51,3.86,1.65,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\n449,PTPTDP,S184,4.2,4.2,0.75,10.3,0.54,51.9,28.5,1.82,1539,5.25,3.6,1.4,O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\n450,PBDT_TEH-TBTT_EHi (P1),S185,6.7,6.48,0.6,17.77,0.631,33.4,7.9,4.21,1313,4.64,3.1,1.54,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\n451,PBDT_TEH-TBTT_HDo (P2),S185,4.45,4.37,0.6,15.21,0.486,22,5.5,3.98,1313,4.63,3.17,1.46,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\n452,PBDT_TEH-TBT_HD (P3),S185,7.5,7.32,0.633,18.15,0.652,22.9,6.1,3.77,1426,4.78,3.22,1.56,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\n453,BFR2,S186,3.91,3.74,0.89,7.25,0.606,66,30,2.2,926,5.2,3.61,1.59,CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\n454,BFS3,S186,5.92,5.67,0.9,10.82,0.608,74.8,34,2.2,1823,5.2,3.62,1.58,CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\n455,BFS4,S186,7.16,7.02,0.9,13.19,0.603,73.6,32,2.3,1655,5.15,3.59,1.56,CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\n456,BFS4b,S186,7.8,7.38,0.9,14.2,0.611,128.8,46,2.8,1655,5.15,3.59,1.56,CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\n457,PBDTTT-E,S187,4.16,4.16,0.66,11.53,0.547,92.4,33,2.8,768,5.04,3.19,1.63,O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\n458,PBDTTT-E-T,S187,6.21,6.21,0.68,14.59,0.626,71.4,21,3.4,900,5.09,3.22,1.58,O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\n459,PBDTTT-C,S187,6.43,6.43,0.7,15.51,0.592,77.7,21,3.7,738,5.07,3.21,1.6,O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\n460,PBDTTT-C-T,S187,7.59,7.59,0.74,17.48,0.587,64,20,3.2,870,5.11,3.25,1.58,O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\n461,PBDTBT (Z3),S188,1.95,1.95,0.84,6.28,0.369,30.2,23.2,1.3,940,4.8,2.95,1.85,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\n462,PBDTBT (Z4),S188,1.28,1.28,0.4,5.27,0.606,23,19.2,1.2,972,5.2,3.65,1.55,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\n463,PDST-BDD,S189,5.95,5.95,1,10.8,0.551,91.7,53,1.73,1396,5.52,3.69,1.83,CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\n464,PBDT-BDD,S189,6.67,6.67,0.86,10.68,0.723,13.6,11.5,1.18,1212,5.3,3.5,1.8,CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\n465,PDST-TT,S189,4.48,4.48,0.98,10.15,0.45,33.1,12,2.76,1102,5.5,3.87,1.63,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\n466,PDST-DPP,S189,3.14,3.14,0.88,6.59,0.541,220.4,95,2.32,1537,5.47,4.01,1.46,CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\n467,PBT-S,S190,6.7,6.7,0.64,14.9,0.703,40.5,14.4,2.82,1296,5.01,2.98,1.66,CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\n468,PBT-SO2-M,S190,1.82,1.82,0.81,5.95,0.379,48.5,14.2,3.41,1360,5.23,3.16,1.68,CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\n469,PBT-SO2-H,S190,6.52,6.52,0.71,14.6,0.629,35.7,14.3,2.5,1360,5.16,3.14,1.64,CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\n470,PBT-T,S191,5.56,5.45,0.6,13.7,0.677,128.8,44.1,2.92,1208,4.95,3.12,1.67,CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\n471,PBT-OP,S191,7.5,7.41,0.78,13.4,0.718,74.7,30.6,2.44,1229,5.17,3.14,1.7,CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\n472,PBDT-Tz-TPD (P1),S192,0.27,0.27,0.82,1.05,0.32,110,26.3,3.8,927,5.65,3.84,1.81,CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\n473,PBDT-Tz-DPP (P2),S192,1.63,1.63,0.44,7.6,0.49,76.4,17.3,4.4,1187,5.18,3.84,1.4,CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\n474,PBDT-Tz-TT (P3),S192,2.3,2.3,0.44,9.5,0.55,133.8,25.7,5.2,1014,5.09,3.84,1.39,CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\n475,PTTBDT-FTT,S193,7.71,7.39,0.77,14.7,0.68,61.5,25,2.46,1030,5.31,3.76,1.55,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\n476,PBT-TVT,S194,8.13,8.13,0.81,16,0.627,121.9,19.5,6.25,1198,5.29,3.76,1.53,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\n477,PBDTBzT-DTffBT,S195,7.3,7.16,0.9,12.93,0.627,40.5,22,1.84,1377,5.47,3.73,1.74,CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\n478,PBDTT-DTffBT,S195,5.35,5.32,0.94,9.83,0.579,28.8,24,1.2,1164,5.36,3.6,1.76,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\n479,PTOBDTDTBT,S196,6.21,6.13,0.8,11.94,0.651,154.8,72,2.15,1601,5.4,3.73,1.67,CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\n480,PQ1,S197,1.08,1.08,1.01,2.12,0.507,61.1,34.7,1.76,1627,5.61,3.65,1.96,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\n481,PQ2,S197,3.8,3.8,0.8,7.68,0.621,82.7,33.9,2.44,1629,5.28,3.31,1.97,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\n482,PQ3,S197,1.09,1.09,0.78,2.67,0.524,68.9,48.2,1.43,1905,5.31,4.02,1.29,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\n483,PQ4,S197,2.83,2.83,0.94,6.17,0.488,51.6,32.6,1.58,1885,5.59,3.86,1.73,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\n484,PBDT2FBT-T1,S198,5.46,5.36,0.98,9.62,0.597,49.3,28.1,1.75,1277,5.47,3.58,1.75,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\n485,PBDT2FBT-T2,S198,5.22,5.11,0.9,10.6,0.547,48.6,42.8,1.13,1441,5.37,3.61,1.73,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\n486,PBDT2FBT-T3,S198,6.48,6.45,0.86,12.3,0.614,102.1,48.2,2.11,1605,5.31,3.62,1.7,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\n487,PBDT2FBT-T4,S198,2.17,2.15,0.84,6.35,0.405,109.5,33.8,3.24,1769,5.3,3.63,1.68,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\n488,PTIPS-BDT-TT (P1),S199,5.76,5.76,0.82,12.75,0.55,20.9,11,1.9,872,5.6,3.91,1.69,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\n489,PTIPS-BDT-TT (P3),S199,4.11,4.11,0.79,9.47,0.55,18.7,11,1.7,890,5.6,3.89,1.71,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\n490,PTIPS-BDT-TT (P2),S199,3.16,3.16,0.78,8.38,0.48,41.8,19,2.2,842,5.61,3.94,1.67,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\n491,PBDTTT-S,S200,6.22,6.22,0.76,14.1,0.58,18,10,1.8,788,5.12,3.49,1.65,CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\n492,PTB2,S201,5.1,5.1,0.58,14.1,0.624,23.2,16.8,1.38,768,4.94,3.22,1.59,CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\n493,PTB7,S201,7.4,7.4,0.74,14.5,0.69,97.5,46.4,2.1,786,5.15,3.31,1.68,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\n494,PTBF2,S201,3.2,3.2,0.68,11.1,0.422,26.7,11.2,2.38,804,5.41,3.6,1.75,O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\n495,PBB3,S201,2.04,2.04,0.63,6.37,0.51,181.3,91.1,1.99,1287,4.95,3.28,1.44,O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\n496,PBDT-CPDTO (P1),S202,2.72,2.72,0.86,4.97,0.55,32.7,21.8,1.5,790,5.44,3.15,1.91,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\n497,PSB-CPDTO (P2),S202,2.2,2.2,0.89,4.13,0.51,16.8,11.8,1.42,762,5.41,3.34,1.72,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\n498,PCz-CPDTO (P3),S202,0.13,0.13,0.74,0.43,0.35,87.2,24.6,3.54,749,5.79,3.04,2.32,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\n499,PFL-CPDTO (P4),S202,0.03,0.03,0.68,0.11,0.28,28.1,17.9,1.57,734,5.92,3.06,2.39,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\n500,PBnDT-DTBT,S203,5,4.7,0.87,10.03,0.573,70,41.2,1.7,1105,5.4,3.13,1.7,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\n501,PBnDT-DTffBT,S203,7.2,6.9,0.91,12.91,0.612,87.9,33.8,2.6,1141,5.54,3.33,1.7,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\n502,PBDT-DODTBT,S204,4.02,4.02,0.76,8.96,0.59,25.7,9.5,2.7,1028,5.17,3.61,1.64,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\n503,PTG1,S205,4.32,4.32,0.84,10.59,0.49,51.8,20.2,2.56,1048,5.56,3.63,2.03,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\n504,P(BDT-TBTF),S206,6.21,6.04,0.88,13.21,0.534,29.8,11.1,2.68,1140,5.36,3.19,1.9,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\n505,PTG1,S206,4.23,4.05,0.83,10.16,0.502,52.5,20.2,2.6,1048,5.44,3.44,1.92,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\n506,PBDT-TPA (P1),S207,3.17,3.09,0.86,9.4,0.39,12.7,10.1,1.25,1127,5.38,3.57,1.93,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\n507,PBDT-TPA (P2),S207,3.05,2.95,0.8,10.77,0.35,12.8,9.8,1.3,1434,5.22,3.53,1.74,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\n508,PDPAT-BDT-BT,S208,3.27,3.27,0.87,7.61,0.498,109,25.4,3.08,1051,5.42,3.6,1.82,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\n509,PBDT-OBT,S209,5.64,5.5,0.82,12.53,0.549,40.9,19.2,2.13,1144,5.32,3.58,1.67,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\n510,PBDT-FBT,S209,6.21,6.08,0.86,12.05,0.599,58.6,22.7,2.58,1259,5.41,3.72,1.63,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\n511,PBnDT-FTAZ,S210,4.1,3.4,0.78,7.8,0.544,34.4,18.3,1.88,1082,5.46,3.42,2.04,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\n512,PBnDT-FTAZ,S210,5.8,5.5,0.76,11.4,0.642,76.6,36.5,2.1,1082,5.51,3.48,2.03,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\n513,PBnDT-FTAZ,S210,7.7,7.3,0.78,13.3,0.705,119,55.2,2.16,1082,5.59,3.57,2.02,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\n514,PBnDT-FTAZ,S210,6.4,6,0.75,12.7,0.633,156,71.4,2.18,1082,5.51,3.49,2.02,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\n515,PNDT-DTPyT,S211,6.2,6.07,0.71,14.16,0.617,36.6,17.1,2.14,1016,5.36,3.42,1.53,CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\n516,PQDT-DTPyT,S211,5.57,5.32,0.75,13.49,0.551,49.3,21.7,2.27,1017,5.5,3.44,1.56,CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\n517,PBnDT-DTPyT,S211,6.32,6.11,0.85,12.78,0.582,380,104.4,3.64,1106,5.47,3.44,1.51,CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\n518,PTIPSBDT-DFDTBTz,S212,2.92,2.92,0.89,6.81,0.48,50,20,2.5,1134,5.59,3.59,2,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\n519,PTIPSBDT-DTBTz,S213,5.53,5.53,0.8,12.69,0.55,57,23,2.5,1098,5.4,3.45,1.95,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\n520,PBDT-DTBTz,S213,2.88,2.88,0.77,7.87,0.48,40,15,2.1,737,5.26,3.29,1.97,CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\n521,PBDFNTDO,S214,4.71,4.71,0.87,9.14,0.592,18.3,10.7,1.71,766,5.33,3.4,1.65,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\n522,PBDTPF-DTBT,S215,7.02,6.9,0.82,13.11,0.653,32,13.9,2.3,1297,5.39,3.66,1.73,CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\n523,BDT-BT-2T,S216,5.4,5.4,0.75,11.2,0.64,128.5,47.6,2.7,1241,5.18,3.55,1.63,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\n524,BDT-FBT-2T,S216,7.7,7.7,0.85,13.3,0.68,136.9,65.2,2.1,1277,5.33,3.63,1.7,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\n525,BDT-BT-2Fu,S216,3.7,3.7,0.86,7.9,0.55,56.1,25.5,2.2,1209,5.36,3.59,1.77,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\n526,BDT-FBT-2Fu,S216,4.4,4.4,0.86,8.7,0.59,79.4,34.5,2.3,1245,5.28,3.6,1.68,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\n527,PBDT-ffBT (P1),S217,0.51,0.41,0.55,3.19,0.29,40.7,22.6,1.8,1221,5.64,3.39,1.71,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\n528,PBDT-BT (P2),S217,3.52,3.43,1.03,7.05,0.48,81.5,28.1,2.9,1349,5.47,3.13,1.69,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\n529,PBDT-TffBT (P3),S217,2.93,2.82,0.86,7.72,0.43,58.3,20.1,2.9,1384,5.52,3.15,1.65,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\n530,PBDT2FBT,S218,3.47,3.29,0.94,7.21,0.519,32.6,18.9,1.72,1305,5.6,3.59,1.76,CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\n531,PBDT2FBT-O,S218,4.53,4.26,0.9,7.87,0.647,44.8,24.4,1.83,1309,5.48,3.59,1.79,CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\n532,PBDT2FBT-T,S218,6.37,6.16,0.98,10.6,0.578,27.1,21.2,1.27,1277,5.55,3.58,1.75,CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\n533,PBDT2FBT-T-O,S218,3.65,3.31,0.84,7.87,0.528,29,17.8,1.63,1309,5.41,3.69,1.72,CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\n534,PSeB1,S219,5.47,5.39,0.602,15.4,0.59,15,8.9,1.68,864,5.05,3.27,1.6,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\n535,PSeB2,S219,6.87,6.46,0.64,16.8,0.64,41,15.3,2.68,960,5.04,3.26,1.6,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\n536,PSeB3,S219,6.13,5.84,0.635,14.6,0.66,52.1,28.5,1.83,864,5.05,3.27,1.6,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\n537,PBDTTTBO,S220,5.9,5.76,0.85,11.8,0.59,246.8,60.2,4.1,1144,5.46,3.68,1.78,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n538,PBDTTTBS,S220,3.3,3.25,0.66,10.1,0.5,157.9,45.1,3.5,1208,5.29,3.6,1.69,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n539,PBDTTTBO,S220,4.7,4.61,0.79,11.9,0.5,221.9,56.9,3.9,1256,5.4,3.71,1.69,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n540,PBDTSTBO,S220,7.6,7.52,0.86,13.9,0.64,275.9,67.3,4.1,1256,5.46,3.68,1.78,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\n541,PBDTTSBS,S220,3,2.87,0.67,9.5,0.49,119.9,38.7,3.1,1304,5.29,3.73,1.56,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n542,PBDTSTBS,S220,4,3.88,0.67,11.4,0.52,160.5,47.2,3.4,1304,5.29,3.6,1.69,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\n543,PBDTSSBO,S220,3.3,3.26,0.78,10,0.42,197.9,52.1,3.8,1352,5.4,3.71,1.69,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\n544,PBDTSSBS,S220,2.4,2.38,0.66,8.3,0.44,87.4,31.2,2.8,1400,5.29,3.73,1.56,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\n545,PBDTBT,S221,5.06,5.06,0.88,10.73,0.536,31.7,17.3,1.83,1164,5.34,3.23,1.74,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n546,PBDTBSe,S221,2.2,2.2,0.81,5.36,0.506,39.4,24.9,1.58,1212,5.3,3.47,1.66,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n547,PBDT-DFBO,S222,5.9,5.6,0.83,10.6,0.647,74.7,36.1,2.07,981,5.34,3.43,1.85,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\n548,PBDTT-DFBO,S222,4.8,4.5,0.86,9.1,0.586,58.9,29.3,2.01,1113,5.44,3.59,1.81,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n549,PBDTF-DFBO,S222,6.6,6.5,0.83,12.7,0.62,86,38.4,2.24,1081,5.4,3.61,1.77,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\n550,PinBDFID,S223,0.59,0.59,0.737,1.66,0.486,76.2,33.1,2.3,1731,5.7,3.8,1.6,O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\n551,PoutBDFID,S223,0.3,0.3,0.641,1.306,0.36,33.1,17.4,1.9,1731,5.7,3.8,1.7,O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\n552,P1,S224,4.8,4.8,0.888,8,0.67,92.5,37,2.5,737,5.39,3.56,1.83,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\n553,P2,S224,0.8,0.8,1.005,2,0.39,65.3,27.2,2.4,733,5.67,3.74,1.93,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\n554,P4,S224,2.1,2.1,0.792,5,0.52,100.8,40.3,2.5,787,5.37,3.94,1.43,CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\n555,PBDT-TPD (P1),S225,5.2,5.2,0.94,10.8,0.51,28.4,12,2.37,737,5.56,3.75,1.8,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n556,PBDT-TPD (P2),S225,2.6,2.6,0.96,6.2,0.43,52.7,20.6,2.56,737,5.66,3.87,1.84,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n557,PBDT-TPD (P3),S225,4.8,4.8,0.93,10,0.51,35.9,16.1,2.23,793,5.6,3.82,1.84,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n558,PBDT-TPD (P5),S225,0.95,0.95,0.76,2.9,0.43,12.5,8.3,1.5,901,5.49,3.7,1.84,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\n559,PBDT-TPD (P7),S225,3.9,3.9,0.89,7.6,0.57,369.4,131,2.82,1126,5.56,3.7,1.88,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\n560,PBDT-TPD (P8),S225,3.5,3.5,0.76,9,0.51,37,11.6,3.19,957,5.54,3.78,1.84,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\n561,PBDT-TPD (P9),S225,0.2,0.2,0.66,1.2,0.26,42,19.9,2.11,1126,5.66,3.83,1.86,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\n562,PBDT-TPD (P10),S225,3.6,3.6,0.87,7.2,0.58,94.4,41.6,2.27,1182,5.56,3.7,1.88,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\n563,PBDT-TPD (P11),S225,0.7,0.7,0.92,2.3,0.34,52.7,22.9,2.3,1182,5.73,3.78,1.89,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\n564,TPO(CO)(2EH/C1),S226,6.1,6.1,1.05,10.3,0.57,42.4,12.7,3.3,799,5.41,3.62,1.79,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n565,TPO(CO)(2EH/C3),S226,6.5,6.5,1.08,10.7,0.57,55.3,15.8,3.5,827,5.41,3.62,1.79,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n566,TPO(CO)(2EH/C7),S226,6.7,6.7,1.05,10.6,0.6,74.7,20.6,3.6,883,5.41,3.62,1.79,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n567,TPO(CO)(2EH/C11),S226,4.6,4.6,1.06,7.7,0.57,94.3,27.2,3.5,939,5.41,3.62,1.79,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n568,TPO(CO)(2EH/C13),S226,4.1,4.1,1.05,7,0.56,78.3,26.3,3,967,5.41,3.62,1.79,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n569,TPD(2EH/C8),S226,6.5,6.5,1,11.1,0.58,51.4,16.4,3.1,869,5.29,3.41,1.88,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\n570,PBDTTPD,S227,3.87,3.87,0.99,8.7,0.453,34,18.9,1.8,1033,5.54,3.52,1.85,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n571,PBDTTPD-HT,S227,6.08,6.08,0.92,10.94,0.604,23.4,14.6,1.6,1202,5.3,3.59,1.86,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n572,INDT-T,S228,2.35,2.35,0.59,6.88,0.58,49.4,15.7,3.15,1177,4.24,3.02,1.57,O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\n573,PBDTBT (P1),S229,2.54,2.38,1,5.36,0.47,179.5,40.8,4.4,1185,5.53,3.57,1.69,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\n574,PBDTTPD (P2),S229,1.33,1.18,0.91,3.22,0.45,72.5,29,2.5,1286,5.52,3.48,1.7,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\n575,P1,S230,7.14,7.02,0.96,13.2,0.559,36,30,1.2,1217,5.42,3.66,1.76,CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\n576,P2,S230,1.82,1.68,0.72,7.4,0.341,32,24.6,1.3,1345,5.34,3.6,1.74,CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\n577,PBDTT-DTTPD,S231,4.82,4.74,0.89,8.05,0.68,41,20,2,1202,5.43,3.55,1.88,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n578,PBDTTVT-DTTPD,S231,6.04,5.97,0.87,10.9,0.63,58.1,25.3,2.3,1418,5.4,3.53,1.87,CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\n579,P1,S232,2.74,2.7,0.87,6.69,0.46,52.8,24,2.2,834,5.59,3.48,1.6,CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\n580,P2a,S232,2.94,2.88,0.71,7.7,0.53,41.8,19,2.2,787,5.66,3.63,1.54,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\n581,P2b,S232,3.07,3.01,0.78,7.05,0.55,168,40,4.2,787,5.63,3.63,1.51,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\n582,P2c,S232,3.04,3.01,0.76,8.46,0.47,180.6,43,4.2,787,5.69,3.64,1.57,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\n583,P3,S232,1.36,1.32,0.75,3.66,0.48,161,35,4.6,787,5.64,3.66,1.53,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\n584,POBDTPD,S233,4.7,4.5,0.7,10.6,0.64,43,25.1,1.71,793,5.23,4,1.38,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\n585,PEBDTPO,S233,5.3,5.1,0.72,13.5,0.54,56,39.7,1.41,793,5.37,4.06,1.38,CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\n586,PBDTTID,S234,3.12,3.12,0.8,6.5,0.6,52.3,20.4,2.56,1176,5.4,3.78,1.53,CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\n587,PID1,S235,3.28,3.28,0.85,7.06,0.547,34.8,12,2.9,773,5.44,3.55,1.81,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n588,PID2,S235,3.05,3.05,0.88,5.94,0.586,32,12.3,2.6,773,5.52,3.4,1.85,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n589,PPB1,S235,5.97,5.97,0.86,10.4,0.666,37.2,18.6,2,737,5.38,3.55,1.84,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n590,PPB2,S235,4.48,4.48,0.88,8.23,0.622,27.9,13.3,2.1,737,5.4,3.55,1.84,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n591,PBTCT,S236,1.13,1.13,0.62,3.39,0.53,28,13.3,2.1,740,5.25,2.75,2.18,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n592,PBTCTO,S236,3.9,3.9,0.72,8.76,0.62,24.2,10.5,2.3,608,5.4,3.42,1.85,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n593,PBTPDO,S236,4.84,4.84,0.73,10.68,0.62,25.3,11.5,2.2,664,5.42,3.51,1.75,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n594,PBTFDO,S236,0.27,0.27,0.79,1.2,0.45,22,11.6,1.9,660,5.45,3.92,1.57,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\n595,PBT8PT,S236,6.78,6.78,0.88,12.37,0.62,60,23,2.6,813,5.36,3.51,1.85,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\n596,PTP8,S237,6.18,6.18,0.96,11,0.585,26.1,12.5,2.08,945,5.59,3.62,1.78,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\n597,PTN8,S238,3.35,3.35,0.97,8.28,0.417,44.1,20.3,2.17,930,5.6,3.81,1.79,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\n598,P1,S239,2.18,2.18,0.87,4.75,0.45,39.4,11.5,3.43,776,5.49,3.53,1.78,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\n599,P2,S239,4.33,4.33,0.93,6.66,0.6,13.4,7,1.9,748,5.33,3.47,1.63,CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\n600,PBDF-T1,S240,9.23,8.87,0.91,13.49,0.755,32.8,23.4,1.4,1169,4.74,2.54,1.83,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\n601,PBDT-T1,S240,8.12,8,0.86,13.13,0.718,56.2,26.8,2.1,1201,4.8,2.52,1.81,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\n602,P(T-QX),S241,3.3,3.3,0.79,6.3,0.659,34.3,13.3,2.6,648,5.57,3.92,1.65,CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\n603,P(BDT-Qx),S241,1.9,1.9,0.77,5,0.503,660.9,38,17.4,1011,5.41,3.63,1.78,CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\n604,P(BDT-DTQx),S241,2.3,2.3,0.65,6.3,0.552,78.2,12.1,6.5,1175,5.43,3.75,1.68,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\n605,PTIPSBDT-DTQX,S242,1.6,1.56,0.79,4.67,0.42,80,30,2.7,1279,5.48,3.66,1.81,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\n606,PTIPSBDT-DFDTQX,S242,6.12,6.08,0.91,10.61,0.62,42,21,1.9,1315,5.62,3.75,1.85,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\n607,PBDT-PTQ,S243,4.39,4.39,0.65,12.5,0.54,11.1,10.1,1.1,1307,5.11,3.64,1.62,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\n608,PBDT-PTTQ,S243,3.58,3.58,0.66,10.53,0.52,13.5,12.3,1.1,1695,5.18,3.62,1.62,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\n609,PBDT-TQ,S243,2.62,2.62,0.72,8.13,0.45,25,22.7,1.1,1098,4.99,3.62,1.61,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\n610,PBDT-TTQ,S243,1.52,1.52,0.62,4.8,0.51,85.6,71.3,1.2,1318,5.08,3.61,1.62,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\n611,PBDT-DTQx,S244,5.12,5.12,0.72,11.47,0.62,38.4,19.9,1.93,1161,5.16,3.68,1.38,CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\n612,PBDT-TFQ,S245,8,7.8,0.76,17.9,0.576,71,46.1,1.54,1154,5.52,3.3,1.73,CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\n613,PBDTDTQx-O,S246,3.06,3.06,0.71,7,0.615,186,84,2.22,1175,5.12,3.38,1.74,CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\n614,PBDTDTQx-T,S246,5,5,0.76,10.13,0.643,80.5,49.5,1.63,1307,5.12,3.45,1.67,CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\n615,PBDT-DTQx,S247,3.9,3.9,0.83,11.71,0.4,14.6,8.5,1.71,1010,5.35,3.6,1.72,CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\n616,PBDTDT(Qx-2)-O,S248,4.44,4.44,0.91,9.38,0.52,23.7,11.9,1.99,1235,5.29,2.77,1.9,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\n617,PBDTDT(Qx-2)-T,S248,6.31,6.31,0.95,10.82,0.614,19.5,11.6,1.69,1367,5.41,2.92,1.82,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\n618,PBDTDT(Qx-3)-T,S249,6.9,6.9,0.94,11.28,0.647,97,59,1.64,1307,5.51,3.57,1.78,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\n619,P0F,S250,2.9,2.9,0.832,6.37,0.54,88.8,32.9,2.7,1162,4.98,3.18,1.8,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\n620,P1F,S250,3.1,3.1,0.872,6.52,0.55,89.3,27.9,3.2,1180,5.07,3.27,1.8,CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\n621,P2F,S250,3.7,3.7,0.914,6.84,0.59,101.5,33.4,3.04,1198,5.08,3.27,1.81,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\n622,PBDT-DFQX-PP,S251,3.96,3.96,0.89,8.66,0.514,43.2,20.8,2.08,1363,5.35,3.53,1.83,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\n623,PBDT-DFQX-TP,S251,6.08,6.08,0.82,12.34,0.601,63.9,40.1,1.59,1343,5.25,3.52,1.78,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\n624,PBDT-DFQX-PT,S251,6.54,6.54,0.85,12.13,0.635,40.4,24.7,1.63,1343,5.29,3.58,1.75,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\n625,PBDT-DFQX-TT,S251,7.68,7.68,0.86,12.77,0.699,81.3,44.5,1.82,1322,5.2,3.5,1.72,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\n626,PFQBDT-TR1,S252,5.7,5.7,0.84,11.1,0.61,64,25,2.56,1343,5.89,3.61,1.7,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\n627,PFQBDT-T2R2,S252,3.4,3.4,0.96,6.5,0.54,66,30,2.2,1455,5.87,3.63,1.77,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\n628,PBDTTFTQ-EH,S253,7.29,7.15,0.78,13.2,0.708,181.1,64.7,2.79,1325,5.29,3.05,1.68,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\n629,PBDTTFTQ-DO,S253,7.61,7.42,0.88,11.4,0.759,250.1,76,3.29,1304,5.37,3.03,1.72,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\n630,PBDTTFTTQ-EH,S253,6.82,6.65,0.72,13.4,0.708,101.4,18.5,5.49,1549,5.12,3.03,1.66,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\n631,PBDTTFTTQ-DO,S253,7.25,7.09,0.85,11.3,0.757,863.6,136,6.35,1529,5.31,2.99,1.72,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\n632,PTTPPz-BDT,S254,4.25,4.25,0.74,9.79,0.582,191.8,57.5,3.33,1253,5.29,3.08,1.7,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\n633,PTTPPz-BDTT,S254,4.86,4.86,0.7,11.1,0.625,71.8,24.2,2.96,1385,5.34,3.15,1.59,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\n634,PBDT-PQD1,S255,4.9,4.9,0.98,10.4,0.48,283.5,113.4,2.5,1712,5.97,3.79,1.64,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\n635,PBDT-PQD2,S255,3.5,3.5,1.08,7.6,0.43,354.2,98.4,3.6,1488,5.96,3.74,1.62,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\n636,PBDT-PQD3,S255,2.9,2.9,1.03,7.3,0.39,573.1,179.1,3.2,1356,5.82,3.72,1.64,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\n637,PT-PQD,S255,2.9,2.9,1,7.7,0.38,132.9,30.9,4.3,993,5.83,3.83,1.52,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\n638,O-HD,S256,4.1,4.1,0.71,9.4,0.61,91.6,42.8,2.14,1189,5.15,3.28,1.45,CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\n639,BO-BO,S256,0.93,0.93,0.59,3.4,0.46,82.3,33.2,2.48,1189,5.14,3.34,1.51,CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\n640,PU-O,S256,1.4,1.4,0.62,5.2,0.43,54.8,27.8,1.97,1189,5.1,3.31,1.36,CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\n641,PBDT-DPP (P1),S257,4.35,4.35,0.64,11.27,0.602,130,40,3.4,1221,5.3,3.8,1.5,CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\n642,PBDT-DPP (P2),S257,4.43,4.43,0.7,12.1,0.524,320,93,3.5,1189,5.3,3.8,1.5,CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\n643,PBDT-DPP (P3),S257,2.69,2.69,0.68,8.75,0.453,72,32,2.2,1189,5.4,3.9,1.5,CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\n644,PBDT-DPP (P4),S257,2.95,2.95,0.66,13.6,0.329,730,130,5.5,1241,5.4,3.9,1.5,CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\n645,PTIPSBDT?DPP,S258,8,7.92,0.76,16.21,0.65,190,76,2.5,1437,5.44,4,1.44,CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\n646,PBDTF-DPP,S259,3.5,3.5,0.69,10.46,0.489,141.8,26.4,5.37,1097,5.16,3.64,1.44,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\n647,PBDTF-DPPF,S259,5.1,5.1,0.72,12.64,0.565,169.3,30.5,5.55,1065,5.24,3.74,1.47,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\n648,PBDT-DPP,S259,1,1,0.62,3.87,0.4,152,28.9,5.26,997,5.05,3.4,1.56,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\n649,PBDT-DPPF,S259,2.9,2.9,0.63,8.78,0.533,154.3,29.5,5.23,965,5.15,3.44,1.59,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\n650,P1,S260,1.93,1.93,0.81,6.27,0.369,58.3,30.7,1.9,1353,5.2,3.56,1.64,CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\n651,P2,S260,2.6,2.6,0.78,5.15,0.581,49.3,28.3,1.74,1453,5.26,3.89,1.37,CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\n652,PBDTBPA(H)-DPP,S261,5.58,5.58,0.74,13.17,0.57,71.3,-,-,1349,5.25,3.86,1.39,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\n653,PBDTBPA(F)-DPP,S261,4.04,4.04,0.68,9.89,0.5,24.3,-,-,1421,5.2,3.91,1.29,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\n654,PBDTDPPcbp,S262,1.3,1.2,0.68,4.11,0.448,72.9,33,2.21,1463,5.39,3.57,1.82,CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\n655,PCBTDPPcbp,S262,1.2,1.1,0.8,4.72,0.319,70.8,28.1,2.52,1422,5.43,3.38,2.05,CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\n656,PDPP2TzBDT,S263,3.2,3.2,0.98,6.2,0.53,326.3,85.2,3.83,1191,5.51,3.98,1.53,CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n657,PDPP2Tz2T,S263,5.1,5.1,0.92,8.8,0.63,196,108.9,1.8,1167,5.46,3.99,1.47,CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n658,PDPP2TzDTP,S263,5.6,5.6,0.69,14.9,0.54,274.4,88.5,3.1,955,5.18,3.9,1.28,CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\n659,PffBT-T4-2HD,S264,7.2,7,0.73,14.8,0.644,25.8,13.9,1.86,976,5.21,3.56,1.65,CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\n660,\"PffBT-T3(1,3)\",S264,3.9,3.7,0.77,10.6,0.453,56,37.7,1.49,894,5.35,3.75,1.6,CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\n661,\"PffBT-T3((1,2)-1\",S264,10,9.7,0.82,18.5,0.641,129,72.2,1.79,1759,5.31,3.68,1.63,FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\n662,\"PffBT-T3(1,2)-2\",S264,10.7,10.5,0.82,18.7,0.683,109.6,66.1,1.66,1731,5.31,3.68,1.63,FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\n663,PffBT-T2,S264,4.5,4.3,0.88,10.1,0.486,98,58.4,1.68,1539,5.38,3.77,1.61,CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\n664,EC12-DT,S265,6.59,5.75,0.861,13.3,0.575,69,33,2.1,1799,5.51,3.8,1.71,CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\n665,EC12-OD,S265,3.63,3.57,0.873,7.37,0.564,98,58,1.7,1687,5.5,3.77,1.73,CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\n666,EHD-HD,S265,2.53,2.41,0.931,4.32,0.629,48,34,1.4,1687,5.57,3.85,1.72,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\n667,EHD-BO,S265,3.7,3.42,0.811,9.3,0.491,66,51,1.3,1575,5.45,3.76,1.69,CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\n668,EBO-BO,S265,3.09,2.93,0.834,8.61,0.43,33,25,1.4,1463,5.44,3.76,1.68,CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\n669,PT-ID1,S266,0.92,0.92,0.87,1.76,0.6,36.1,17.2,2.1,933,5.49,3.91,1.58,CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\n670,PTT-ID1,S266,1.74,1.74,0.84,3.9,0.53,127.8,37.6,3.4,989,5.43,3.88,1.55,CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\n671,PBDT-ID,S266,1.91,1.91,0.71,7.93,0.34,32.6,21.9,1.5,959,5.2,3.66,1.54,CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\6)=O)C=C4\n672,PBDT?IBTI,S267,6.41,6.41,0.77,11.71,0.71,115.8,43.5,2.67,1485,5.24,3.72,1.71,CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\n673,PMIM,S268,1.64,1.5,0.73,6.24,0.36,42.2,20.1,2.1,931,5.93,3.84,1.53,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\n674,PT-MIM,S268,3.55,3.4,0.7,10.56,0.48,24.1,13.4,1.8,1013,5.78,3.83,1.57,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\n675,PBDTO-MIM,S268,4.98,4.9,0.73,10.7,0.64,190.5,63.5,3,1375,5.87,3.91,1.66,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\n676,PBDTA-MIM,S268,5.36,5.1,0.8,10.2,0.65,277.2,69.3,4,1483,5.94,3.81,1.66,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\n677,PBDT-ID,S269,2.8,2.8,0.85,6.4,0.52,165,33,5,1183,5.81,4.18,1.63,CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\6)=O)C=C4\n678,PBDT-TIT,S269,4.85,4.35,0.79,9.38,0.66,109.2,42,2.6,1347,5.75,4.08,1.68,CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\7)=O)C=C5)S4)S3\n679,PBDT-BTI,S269,7.31,7.31,0.72,14.96,0.68,181.5,55,3.3,1735,5.62,3.99,1.63,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\n680,PBDT-TTI,S269,3.98,3.98,0.66,11.82,0.52,625.5,139,4.5,2123,5.62,3.99,1.63,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\n681,PBDT-IIG,S270,5.86,5.74,0.85,10.48,0.658,54.6,21,2.6,1591,5.38,3.35,1.59,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\n682,PBDT-TIIG,S270,2.55,2.43,0.38,11.74,0.572,95.2,34,2.8,1603,4.96,3.29,1.05,O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\n683,PBDTT?ID,S271,4.76,4.76,0.88,8.95,0.6,88.7,36.8,2.41,1479,5.52,3.92,1.6,O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\n684,PBDTT?FID,S271,7.04,7.04,0.92,11.3,0.68,98.6,37.2,2.65,1515,5.64,4.06,1.58,O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\n685,P1,S272,1.05,1.05,0.75,4,0.34,70.2,23.4,3,698,5.62,3.9,1.72,CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\n686,P2,S272,0.47,0.47,0.85,3.3,0.33,54.8,27.4,2,867,5.61,3.87,1.74,CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\n687,P1,S273,1.19,1.19,0.83,3.71,0.39,65.1,29.6,2.2,666,5.39,3.32,2.07,CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\n688,P2,S273,0.79,0.79,0.81,2.24,0.44,56.3,22.5,2.5,1335,5.3,3.26,2.04,CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\n689,syn-PBDFID,S274,1.44,1.44,0.85,2.89,0.59,343.5,146.8,2.34,1007,5.63,3.9,1.73,CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\n690,anti-PBDFID,S274,0.65,0.65,0.75,1.74,0.48,88.7,34.8,2.55,1007,5.49,3.85,1.64,CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\n691,P1,S275,2.89,2.89,0.69,7,0.6,55.6,28.9,1.9,1401,5.5,3.7,1.8,O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\n692,P2,S275,2.81,2.81,0.65,7.7,0.57,44.2,19.9,2.2,1569,5.5,3.8,1.7,O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\n693,P3,S275,2.28,2.28,0.66,7.4,0.47,24,9.5,2.5,1433,5.6,3.8,1.8,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\n694,P4,S275,0.97,0.97,0.59,4.2,0.39,8.1,6.1,1.3,1601,5.6,3.7,1.9,O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\n695,PBDFTT-C,S276,4.26,4.26,0.54,13.13,0.6,69.2,40.7,1.7,706,5.03,3.63,1.53,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\n696,PBDFTT-EF,S276,5.17,5.17,0.61,15.75,0.538,103.7,61,1.7,754,5.07,3.61,1.53,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\n697,PBDFTT-CF,S276,5.23,5.23,0.63,13.88,0.598,108.7,45.3,2.4,724,5.11,3.6,1.52,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\n698,PBDFTT-S,S276,5.08,5.08,0.59,14.21,0.607,48.8,37.5,1.3,756,5.25,3.61,1.61,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\n699,PBDFTT-ECN,S276,2.28,2.28,0.87,5.88,0.446,39,30,1.3,761,5.44,3.7,1.6,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\n700,PBDFTT-CF-O,S277,5.22,5.22,0.63,13.87,0.597,14,4.7,3,724,4.98,3.18,1.51,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\n701,PBDFTT-CF-T,S277,6.26,6.26,0.78,13.04,0.616,17,4.7,3.6,856,5.21,3.2,1.49,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\n702,P1,S278,2.55,2.39,0.73,6.04,0.54,73.2,23,3.18,1000,5.15,3.36,1.56,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\n703,P2,S278,2.61,2.5,0.67,6.32,0.59,86.5,33.6,2.57,968,5.07,3.29,1.52,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\n704,P3,S278,3.34,3.18,0.68,7.83,0.6,206.5,50.6,4.08,968,5.18,3.53,1.51,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\n705,P4,S278,5.23,5.01,0.65,12.11,0.64,337.5,66.7,5.06,937,5.12,3.56,1.5,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\n706,BDF(2EH/C7),S279,6.6,6.3,0.94,10.8,0.65,26.2,11,2.4,691,5.41,3.44,1.97,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\n707,BDF(2EH/C8),S279,7.4,6.9,0.97,11.2,0.68,40.8,13.4,3,705,5.41,3.44,1.97,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\n708,BDF(2EH/C9),S279,7.3,6.9,0.93,11.3,0.69,34.4,13,2.6,719,5.41,3.44,1.97,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\n709,BDF(2EH/C10),S279,6.3,5.9,0.94,11.2,0.6,36.1,13.8,2.6,733,5.41,3.44,1.97,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\n710,BDT(2EH/C8),S279,7.1,6.7,0.94,12,0.61,49,14.8,3.3,737,5.29,3.44,1.85,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\n711,P9,S280,4.61,4.61,0.8,9.81,0.587,14.3,11.3,1.27,1443,5.31,3.61,1.7,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\n712,P1,S281,2.22,2.22,0.83,5.28,0.51,68,24.9,2.73,1517,5.25,3.2,1.67,CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\n713,P2,S281,4.44,4.44,0.83,8.74,0.612,203.4,75.7,2.69,1535,5.3,3.25,1.68,CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\n714,PTDBD2,S282,7.6,7.6,0.89,13,0.653,108.6,38.5,2.82,978,5.24,3.57,1.67,CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\n715,PTDBD3,S282,4.9,4.9,0.88,10.7,0.521,105.5,45.1,2.34,1063,5.3,3.63,1.67,CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\n716,PTR5b,S283,5,5,0.65,12.2,0.63,76.5,35.6,2.15,1066,5.18,3.28,1.66,CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\n717,PTR7a,S283,0.01,0.01,0.2,0.28,0.25,19.8,12.6,1.57,1317,5.2,3,1.77,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\n718,PTR7b,S283,0.08,0.08,0.3,0.96,0.288,18.9,12.3,1.54,1429,5.22,2.99,1.78,CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\n719,PTR9a,S283,2.8,2.8,0.71,7.23,0.546,28.8,11,2.62,1679,5.23,3.04,1.84,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\n720,PTR9b,S283,2,2,0.71,5.22,0.54,41.5,14.7,2.82,1791,5.32,3.01,1.83,CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\n721,pDTBDT-TTEH,S284,6.74,6.5,0.72,15.77,0.594,80,37,2.16,1319,5.29,3.66,1.63,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\n722,pDTBDT-DTPD,S284,2.83,2.7,0.79,6.64,0.539,42,25,1.68,1374,5.53,3.87,1.66,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\n723,PBT-HD-DPP-C16,S285,2.42,2.42,0.62,6.41,0.609,15.2,9.7,1.58,1557,5.13,3.65,1.48,CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\n724,PBT-T-DPP-C12,S285,5.19,5.19,0.65,12.61,0.634,34.4,20.6,1.67,1689,5.19,3.72,1.47,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\n725,PBT-TIPS-DPP-C16,S285,6.39,6.39,0.75,13.9,0.613,27.6,16.2,1.71,1437,5.25,3.8,1.45,CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\n726,PDPPBDT,S286,3.31,3.28,0.741,7.33,0.61,683.2,122,5.6,1445,5.37,3.39,1.51,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\n727,PDPPDTT,S286,6.11,5.94,0.7,13.64,0.64,64.5,43,1.5,1195,5.36,3.59,1.43,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\n728,PDPPDTBDT,S286,4.75,4.69,0.745,9.8,0.65,75.4,29,2.6,1553,5.35,3.35,1.5,CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\n729,PDTBDT-ID,S287,4.43,4.43,0.7,12.58,0.503,25.8,14.7,1.76,1295,5.38,3.8,1.58,CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\n730,PDTBDT-DTNT,S288,7.52,7.52,0.65,17.51,0.66,62,26.4,2.35,1629,5.51,3.9,1.58,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\n731,PDTP-DTBDT,S289,6.81,6.81,0.83,15.1,0.543,85.2,46.3,1.84,1677,5.44,3.01,1.85,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\n732,P(Ge-DTBT),S290,3.51,3.35,0.66,7.95,0.68,97.5,39,2.5,1127,5.05,3.27,1.56,CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\n733,P(Ge-DTCNBT),S290,6.55,6.03,0.68,14.83,0.7,109.2,42,2.6,1152,5.11,3.54,1.4,CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\n734,P(Ge-CTDCNBT),S290,0.63,0.39,0.68,2.99,0.36,44.4,20.5,2.2,1177,5.14,3.77,1.27,CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\n735,TBTIT-h,S291,9.1,9.1,0.72,17.7,0.71,546,151,3.6,1269,5.1,3.5,1.6,CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\n736,TBTIT-i,S291,5.3,5.3,0.73,13.6,0.54,91,33,2.7,1269,5.2,3.6,1.6,CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\n737,F-BT2,S292,1.66,1.44,0.64,4.48,0.57,134,34.4,3.9,1953,5.44,3.95,1.49,CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\n738,BT2,S292,4.18,3.92,0.62,10.07,0.67,231,59.2,3.9,1935,5.41,3.92,1.49,CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\n739,BTSA5,S293,5.5,5.5,0.85,9.5,0.682,66.2,14.4,4.6,855,5.39,3.55,1.84,O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\n740,P-PDTz-Tdt-HH,S294,1.82,1.82,0.83,4.86,0.45,16.2,13.5,1.2,1391,5.59,3.84,1.75,CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\n741,TTT,S295,4.01,3.85,0.7,10.05,0.548,110.9,29,3.8,859,5.27,3.89,1.38,CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\n742,TPT,S295,4.37,3.91,0.76,12.86,0.399,24.2,13.5,1.8,853,5.32,3.84,1.48,O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\n743,TTfT,S295,1.25,1.17,0.7,3.17,0.53,17.2,10.2,1.7,895,5.44,4.06,1.38,O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\n744,TPfT,S295,2.4,2.29,0.83,6.14,0.449,19.3,10.3,1.9,889,5.45,3.98,1.47,O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\n745,P[T-iI(HD)]-4,S296,2.9,2.9,0.9,5.8,0.55,54.6,26,2.1,821,5.21,3.59,1.62,CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\4C=CC(C)=C5)=O)C3=C2)S1\n746,P[T3(C6)-iI(HD)]-2,S296,6.6,6.6,0.7,15.2,0.62,66.6,18,3.7,1153,5.29,3.71,1.58,O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\n747,P[T3(C6)-iI(SiO)],S296,2.8,2.8,0.66,8.6,0.49,70.4,32,2.2,1313,5.43,3.88,1.55,O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\n748,PDTBDT-BZ,S297,5.54,4.9,0.83,10.28,0.649,28,11.5,2.43,1189,5.3,3.2,1.65,CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\n749,PDTBDT-BZF,S297,7.42,7,0.88,11.47,0.735,70,21,3.33,1207,5.4,3.3,1.71,CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\n750,PDTBDT-BZF2,S297,5.46,5.1,0.9,10.02,0.605,89,23,3.87,1225,5.4,3.3,1.75,CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\n751,DP3,S298,2.73,2.69,0.674,7.06,0.573,37.5,11.3,3.32,1213,5.16,3.46,1.51,CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\n752,DP4,S298,3.75,3.7,0.697,8.37,0.643,88.8,53.8,1.65,1101,5.25,3.59,1.54,CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\n753,PTF1,S299,1.04,1.04,0.72,4.97,0.29,18,9.3,1.9,1106,4.97,3.81,1.56,FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\n754,POF1,S299,1.22,1.22,0.79,5.17,0.3,85.2,19,4.4,974,4.84,3.67,1.63,FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\n755,PTF2,S299,2.13,2.13,0.72,8.7,0.34,54.7,21.2,2.5,1142,4.88,3.74,1.56,FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\n756,POF2,S299,1.6,1.6,0.77,5.25,0.4,75.8,19.2,3.9,1010,4.78,3.62,1.63,FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\n757,MBDT1,S300,4.72,4.64,0.77,10.75,0.57,125.3,53.8,2.33,1151,5.54,3.78,1.76,CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\n758,MBDT2,S300,1.65,1.54,0.75,4.41,0.5,124.7,35.8,3.49,1371,5.43,3.53,1.9,CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\n759,PBTTPD,S301,5.98,5.75,0.9,10.38,0.64,77.3,44.7,1.73,583,5.51,3.36,1.77,CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\n760,PTVTPD,S301,7.16,6.97,0.88,12.32,0.66,57.8,41,1.41,609,5.48,3.32,1.77,CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\n761,PBBTz-Cz,S302,0.95,0.95,0.74,4.21,0.3,5,2.8,1.8,1012,5.7,3.2,1.5,CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\n762,BTT-DTFFBT,S303,5.61,5.61,0.78,11.79,0.61,13.4,11,1.22,1169,5.24,3.54,1.71,CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\n763,PBBTZBT,S304,6.53,6.53,0.801,12.43,0.674,107,51,2.1,1693,5.7,3.9,1.8,CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\n764,PCPDTBT,S305,3.5,3.5,0.65,11.8,0.456,42,28,1.5,564,5.3,3.55,1.4,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\n765,PCPDTFBT,S306,5.81,5.81,0.76,15,0.51,36,23.4,1.54,582,5.15,3.71,1.44,CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\n766,a-PTPTBT-SA,S307,6.41,6.41,0.85,11.2,0.672,60.9,24.3,2.51,1069,5.36,3.52,1.75,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\n767,PBTISi-C6,S308,6.29,6.29,0.825,12.4,0.606,95.7,29,3.3,763,5.45,3.7,1.75,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n768,PBTISi-C8,S308,6.41,6.41,0.803,12.79,0.623,93,30,3.1,791,5.43,3.68,1.75,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n769,PBTISi-EH,S308,5.54,5.54,0.834,12.67,0.531,72.8,26,2.8,791,5.42,3.65,1.77,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n770,PBTIGe-C6,S308,4.77,4.77,0.774,11.96,0.502,78.3,27,2.9,809,5.39,3.64,1.75,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n771,PBTIGe-C8,S308,4.32,4.32,0.745,11.62,0.472,67.5,25,2.7,837,5.38,3.63,1.75,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n772,PBTIGe-EH,S308,3.62,3.62,0.769,9.97,0.467,41.4,18,2.3,837,5.38,3.62,1.76,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n773,PTPDSi-C8,S308,6.83,6.83,0.885,11.8,0.649,52.2,29,1.8,709,5.52,3.79,1.73,CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n774,PGeBTBT,S309,4.5,4.5,0.57,18.6,0.43,98,31,3.16,626,4.78,3.31,1.47,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n775,P-Si,S310,6.6,6.6,0.89,11.5,0.65,52.7,31,1.7,709,5.65,3.92,1.73,CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n776,P-Ge,S310,7.3,7.3,0.85,12.6,0.68,81.6,48,1.7,755,5.6,3.91,1.69,CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n777,PGe1-C8,S311,1.5,1.5,0.53,7.8,0.36,16.9,8.9,1.9,626,5.21,3.85,1.33,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\n778,PGe1-EH,S311,2.9,2.9,0.52,10.5,0.53,21.1,12.4,1.7,626,5.22,3.93,1.43,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n779,PGe2,S311,4.1,4.1,0.8,9.7,0.53,31,16.3,1.9,755,5.66,3.93,1.67,CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\n780,PSDTTT,S312,5.4,5.3,0.69,11.6,0.66,44.4,13.1,3.39,1559,5.4,3.6,1.77,CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\n781,PzNDTTPD,S313,5.26,5.26,0.91,9.03,0.64,56.9,20.7,2.75,956,5.38,3.43,2.04,CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\n782,PzNDTDTBT,S314,3.22,3.22,0.6,8.88,0.605,57.4,32.8,1.75,1191,5.15,3.43,1.76,CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\n783,PzNDTDTBO,S314,5.07,5.07,0.74,10.46,0.655,75.3,50,1.5,1175,5.3,3.38,1.76,CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\n784,P1,S315,2.51,2.51,0.55,11.99,0.38,17,10,1.7,788,4.86,3.26,1.6,CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\n785,P2,S315,4.88,4.88,0.71,13.52,0.51,42,18,2.33,806,5.03,3.34,1.69,CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\n786,PIDT-diphQ,S316,5.69,5.69,0.87,10.9,0.6,165,68.2,2.42,1215,5.33,3.52,1.81,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\n787,PIDT-phanQ,S316,6.24,6.24,0.87,11.2,0.64,234,82.4,2.84,1213,5.28,3.61,1.67,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\n788,PIDT-BTz,S317,2.77,2.77,0.9,7.43,0.414,24.9,13.6,1.83,1465,5.26,2.8,2,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\n789,PIDT-TTz,S317,5.79,5.79,0.89,13.3,0.489,27.6,17.4,1.59,1271,5.21,2.94,1.83,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\n790,PIDT-TZ,S317,3.04,3.04,0.9,8.85,0.381,13.3,8.7,1.53,1211,5.22,2.97,1.82,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\n791,PIDT-DTBT,S317,6.17,6.17,0.82,13.27,0.567,21.3,11.7,1.82,1265,5.24,3.1,1.68,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\n792,PIDSBT-OCH8,S318,2.6,2.6,0.76,8.45,0.41,18.2,10.7,1.7,1341,5.28,3.45,1.6,CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\n793,PIDSFBT-OCH8,S318,1.9,1.9,0.86,6.72,0.32,19.6,11.5,1.7,1377,5.32,3.57,1.68,CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\n794,PIDSBT-C6,S318,3.9,3.9,0.76,11.24,0.45,21.6,10.8,2,1164,5.28,3.51,1.6,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\n795,PIDSFBT-C6,S318,3.8,3.8,0.84,9.67,0.47,14.9,9.3,1.6,1200,5.38,3.61,1.63,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\n796,PIDT-DFBT,S319,6.02,5.87,0.97,11.2,0.554,186.7,61.4,3.04,1105,5.35,3.4,1.79,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\n797,PIDSe-DFBTL,S319,5.48,5.17,0.9,12.1,0.503,66.5,30.1,2.21,1200,5.34,3.48,1.68,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\n798,PIDSe-DFBTM,S319,6.11,5.92,0.89,12.9,0.532,109.7,46.3,2.37,1200,5.34,3.47,1.68,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\n799,PIDSe-DFBTH,S319,6.79,6.61,0.89,13.7,0.563,127.9,61.8,2.07,1200,5.33,3.48,1.68,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\n800,PDIDTBT,S320,0.76,0.76,0.7,3.3,0.33,7,5,1.4,871,5.51,3.07,2.09,CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\n801,PTDIDT,S320,1.65,1.65,0.7,5.3,0.44,5,4,1.25,819,5.36,3.23,2.21,CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\n802,PDIDTDTBT,S320,2,2,0.68,6.2,0.47,13,7,1.86,1035,5.35,3.32,1.85,CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\n803,PBSTBT,S321,3.66,3.47,0.81,8.86,0.488,80.4,38.5,2.09,909,5.32,3.25,1.8,CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\n804,PBSTDTBT,S321,3.78,3.64,0.8,8.8,0.516,35.4,22.4,1.58,1072,5.25,3.55,1.7,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\n805,P-1,S322,4.3,4.3,0.88,9.39,0.52,61,30,2.03,909,5.5,3.6,1.96,CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\n806,P-2,S322,1.4,1.4,0.63,3.53,0.65,80,29,2.76,1409,5.1,3.7,1.64,CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\n807,PBDPTBT,S323,3.08,3.08,0.6,10.34,0.497,10.1,7.4,1.37,907,5.11,3.25,1.52,CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\n808,PBDPTFPP,S323,3.72,3.72,0.75,9.69,0.512,92.1,26.4,3.49,1036,4.89,3.41,1.25,CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\n809,PBDPTTPD,S323,1.34,1.34,0.56,4.95,0.485,19.7,12.3,1.6,1295,5.14,3.13,1.77,CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\n810,PTAT-2,S324,0.37,0.37,0.77,1,0.46,38.6,24.1,1.6,1417,5.12,3.32,1.8,FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\n811,PTAT-3,S324,5.62,5.62,0.66,15,0.58,47.1,18.1,2.6,1080,5.04,3.28,1.76,FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\n812,PTAT-4,S324,2.98,2.98,0.62,9.6,0.5,45.5,18.2,2.5,1080,5.08,3.31,1.77,FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\n813,PTB-8,S324,2.78,2.78,0.83,5.7,0.59,170.8,83.3,2.05,900,5.24,3.34,1.9,CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\n814,pDTTG-TPD,S325,7.2,7.2,0.81,13.85,0.64,17,12.1,1.4,867,5.68,3.88,1.75,CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\n815,PFDTPBT,S326,3.11,3.11,0.74,8.37,0.5,55,20,2.7,1079,5.11,2.64,2.15,CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\n816,PCDTPBT,S326,2.54,2.54,0.72,7.47,0.47,121,27,4.47,1094,5.06,2.67,2.13,CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\n817,PCPDTDTPBT,S326,1.35,1.35,0.48,6.23,0.45,58.5,23.4,2.5,1091,4.9,2.82,1.77,CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\n818,PFDTPQX,S326,3.4,3.4,0.72,8.62,0.55,70,34,2.17,1225,5.06,2.61,2.19,CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\n819,PCDTPQX,S326,2.95,2.95,0.7,8.27,0.51,50.9,30.2,1.68,1240,5.02,2.64,2.18,CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\n820,PCPDTDTPQX,S326,1.38,1.38,0.5,5.64,0.49,36.1,17,2.1,1237,4.88,2.71,1.85,CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\n821,PThTPTI,S327,7.8,7.8,0.87,13.69,0.656,62.7,28.5,2.2,883,5.42,2.77,1.86,CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\n822,PSeTPTI,S328,6.04,6.04,0.85,11.1,0.64,122.5,34.9,3.51,930,5.41,2.88,1.77,CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\n823,PDTCTTTPD,S329,2.59,2.59,0.72,8.35,0.43,44,18,2.44,1436,5.3,3.13,1.72,CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\n824,PDTCTTBT,S329,2.57,2.57,0.64,8.03,0.5,31,20,1.55,1307,5.08,3.38,1.51,CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\n825,PDTCTTPQX,S329,1.91,1.91,0.62,7.33,0.42,14.4,10.2,1.41,1451,5.04,3.46,1.48,CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\n826,P4TBT,S330,2.5,2.5,0.59,9.1,0.49,50,19,2.6,1130,5.2,3.7,1.5,CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\n827,Si4T-BT,S331,2.79,2.79,0.67,9.69,0.43,53,19,2.8,970,5,3.4,1.6,CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\n828,Si4T-TPD,S331,3.46,3.46,0.8,9.42,0.46,26,21,1.2,1100,5.3,3.6,1.7,CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\n829,Si4T-2FBT,S331,5.52,5.52,0.77,14.07,0.51,58,40,1.5,1006,5.1,3.5,1.6,CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\n830,DTBTBT-Bz,S332,3.7,3.7,0.92,6.78,0.6,132,19,6.95,1187,5.2,3.4,1.8,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\n831,DTBTBT-T,S332,3.3,3.3,0.7,8.1,0.59,77,29,2.66,1135,4.9,2.7,2.2,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\n832,DTBTBT-TT,S332,2.3,2.3,0.66,6.41,0.56,17,9,1.89,1191,4.9,4.9,2.2,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\n833,DTAT-Bz,S332,2.7,2.7,0.94,4.55,0.64,46,19,2.42,1125,5.3,3.5,1.8,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\n834,PDITTBT,S333,2.7,2.7,0.88,7.46,0.414,33.4,19,1.76,1295,5.52,3.23,2.15,CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\n835,PDITTDTBT,S333,5.8,5.8,0.92,10.71,0.584,17,8.1,2.1,1459,5.4,3.36,1.87,CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\n836,PFDCTBT,S334,2.8,2.8,0.77,9.5,0.38,16,8.5,1.89,1557,5.32,3.55,1.76,CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\n837,PCDCTBT,S334,3.7,3.7,0.8,10.7,0.43,13,8.2,1.59,1572,5.38,3.61,1.66,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\n838,PCDCTBT-C8,S335,4.59,4.59,0.74,10.3,0.6,61,38.1,1.6,1204,5.31,3.67,1.64,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\n839,PCDCTDTBT-C8,S335,3.53,3.53,0.74,9.2,0.52,30.6,14.1,2.17,1368,5.31,3.65,1.66,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\n840,PCDCTDTDPP-C8,S335,2.35,2.35,0.7,6.7,0.5,20.2,18,1.12,1592,5.24,3.87,1.37,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\n841,PCDCTQX-C8,S335,1.8,1.8,0.78,5.8,0.4,14.2,5.6,2.53,1350,5.25,3.53,1.72,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\n842,PFDCTBT-C8,S336,7,7,0.83,12.57,0.668,94.7,33,2.87,1189,5.3,3.55,1.71,CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\n843,PDTPCBT,S337,2.6,2.6,0.5,10.5,0.499,44,36.4,1.21,982,4.76,3.29,1.5,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\n844,PDTCCBT,S337,4.6,4.6,0.74,10.3,0.6,61,38.1,1.6,1204,5.31,3.67,1.64,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\n845,PSiFDCTPD,S338,2.8,2.7,0.84,7.3,0.44,34.2,16.3,2.1,1470,5.31,3.63,1.88,CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\n846,PSiFDCTBT,S338,4.3,4.2,0.86,8.8,0.56,93.5,37.4,2.5,1341,5.32,3.71,1.76,CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\n847,PSiFDCTDPP,S338,1.5,1.48,0.79,3.78,0.495,16.6,10.4,1.6,1729,5.26,3.85,1.57,CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\n848,PBDCPDT-TPD,S339,6.6,6.6,0.87,12.21,0.622,75,24.5,3.06,1486,5.36,3.2,1.88,CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\n849,PBDCPDT?FBT,S340,5.76,5.76,0.81,12.82,0.555,74.2,49.9,1.48,1393,5.35,3.48,1.67,CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\n850,PIDTTBT,S341,3.8,3.8,0.84,8.32,0.55,28.2,16.6,1.7,1357,5.3,3.4,1.69,CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\n851,PIDTTFBT,S341,4.2,4.2,0.9,10.08,0.46,28.8,24,1.2,1393,5.43,3.5,1.77,CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\n852,PIDTTTPD,S341,4.3,4.3,0.9,7.99,0.6,62.6,31.3,2,1486,5.45,3.18,1.95,CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\n853,PIDTT-DFBT,S342,7.03,7.03,0.95,12.21,0.61,61.9,24,2.58,1216,5.3,3.5,1.78,CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\n854,PTPTPTBT,S343,5.9,5.9,0.76,12.1,0.64,50.7,30,1.69,1875,5.24,3.38,1.73,CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\n855,PTPTPTQX,S343,4.7,4.7,0.74,10.2,0.62,54.4,34,1.6,2021,5.21,3.3,1.8,CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\n856,PIDTCPDT-DFBT,S344,6.46,6.32,0.75,14.59,0.59,42.1,19.6,2.15,2045,5.05,3.28,1.59,CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\n857,PIDTT-T-DFBT,S344,5.26,5.14,0.92,10.4,0.54,32.9,17.3,1.9,1549,5.15,3.2,1.77,CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\n858,PCPDTDFBT,S345,5.6,5.6,0.85,12.6,0.52,50,20,2.5,600,5.34,3.52,1.51,CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\n859,PDTPDFBT,S345,7.9,7.9,0.68,17.8,0.65,50,20,2.5,672,5.26,3.61,1.38,CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\n860,PBDT-BOZ,S346,6.05,6.05,0.887,13.6,0.508,179.8,47.2,3.81,676,5.34,3.45,1.68,CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\n861,PCzDBSe,S347,2.58,2.58,0.75,7.23,0.45,17,14,1.21,779,5.28,3.55,1.73,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\n862,PF-DTBTA,S348,1.3,1.3,1,2.64,0.515,20.2,8.7,2.32,868,5.67,3.43,2.24,CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\n863,PCz-DTBTA,S348,2.75,2.75,0.9,4.68,0.653,296,107.2,2.76,883,5.54,3.36,2.18,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\n864,PPh-DTBTA,S348,1.39,1.39,0.55,4.5,0.561,18.3,8.7,2.11,812,5.2,3.33,1.87,CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\n865,PCDTMBI,S349,3.12,3.12,0.65,10,0.48,182,28.5,6.4,741,5.47,3.82,1.64,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\n866,PCPPDTMBI,S349,0.67,0.67,0.47,4.48,0.32,39.8,15.2,2.6,750,5.54,3.88,1.66,CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\n867,PFDTMBI,S349,0.42,0.42,0.56,2.44,0.31,12.7,8.1,1.6,726,5.61,3.97,1.64,CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\n868,N-P7,S350,5.5,5.5,0.99,9.72,0.574,39.5,16.6,2.38,862,5.37,3.42,1.95,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\n869,PECz-DTQx,S351,6.07,6.07,0.81,11.4,0.658,50.7,24.3,2.09,1160,5.15,3.45,1.7,CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\n870,TQ1,S352,6,6,0.89,10.5,0.64,106.6,41,2.6,648,5.7,3.3,1.7,CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\n871,PTT-DPP (P1),S353,5.4,5.4,0.58,15,0.61,75,14,5.4,1083,5.06,3.68,1.56,O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\n872,PTT-DPP (P2),S353,3,3,0.57,8.9,0.59,78,16,4.9,1001,5.04,3.76,1.58,O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\n873,PDTSTTz,S354,5.59,5.59,0.77,11.9,0.61,13.8,8.7,1.59,918,5.06,2.81,1.81,CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\n874,P1,S355,0.3,0.3,0.82,1.24,0.296,252.6,73.7,3.4,932,5.44,2.91,2.21,CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\n875,P2,S355,0.06,0.06,0.28,0.51,0.337,9.3,4.6,1.78,817,4.76,2.79,1.68,CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\n876,P3,S355,2.86,2.86,0.68,7.85,0.535,9.5,5.6,1.7,944,5.18,3.09,1.85,CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\n877,PCPDTTTz,S356,5.4,5.4,0.75,12.2,0.59,28.2,20,1.41,786,5.34,3.48,1.68,CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\n878,PDTSNTDO.,S357,5.21,5.21,0.88,9.24,0.64,16.3,11.7,1.39,742,5.42,3.46,1.65,CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\n879,PSiF-DBT,S358,5.4,5.4,0.9,9.5,0.507,331.8,79,4.2,732,5.39,3.57,1.82,CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\n880,PDTPBT-C8,S359,1.23,1.23,0.43,6.19,0.46,20.3,14.9,1.37,579,4.89,3.08,1.41,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\n881,PDTPBT-C6,S359,2.06,2.06,0.43,11.1,0.43,21.7,15.6,1.36,523,4.86,3.07,1.42,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\n882,PDTPBT-C5,S359,2.8,2.8,0.54,11.9,0.44,29.2,17.9,1.63,495,4.81,3.08,1.43,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\n883,PDTC,S360,3.74,3.74,0.8,10.04,0.47,20.2,16,1.26,693,5.43,3.25,1.67,CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\n884,PDTSi,S360,2.13,2.13,0.85,6.58,0.37,19.4,13.6,1.43,709,5.44,3.17,1.7,CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\n885,PDTP,S360,1.69,1.69,0.76,4.69,0.53,13.7,10.6,1.29,708,5.16,3.08,1.59,CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\n886,P1,S361,0.8,0.8,0.36,4.2,0.536,12,7,1.71,991,4.9,3.5,1.4,CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\n887,P2,S361,0.7,0.7,0.44,3.69,0.4,25,11,2.27,1027,4.9,3.4,1.5,CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\n888,P3,S361,1.1,1.1,0.58,4.04,0.478,28,12,2.33,1120,5.1,3.4,1.7,CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\n889,P4,S361,2.5,2.5,0.77,4.62,0.688,57,22,2.59,1383,5.1,3.5,1.6,CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\n890,PBBTz-PT,S362,2.3,2.16,0.761,5.91,0.48,65,27,2.41,1694,5.54,3.84,1.7,CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\n891,PBBTz-FT,S362,6.37,6.21,0.881,10.88,0.649,237,107,2.21,1729,5.42,3.69,1.73,CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\n892,HMPBDT,S363,0.1,0.1,0.76,0.34,0.4,21.5,11,1.96,830,5.7,2.65,2.31,CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\n893,PBDTBT,S363,0.6,0.6,0.72,2.06,0.42,11.9,10.1,1.18,964,5.34,3.16,1.78,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\n894,HMPQTN,S364,2.03,2.03,0.76,5.02,0.531,17.6,8,2.2,828,5.39,2.72,2,CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\n895,PQTNBT,S364,2.06,2.06,0.72,5.69,0.503,10.2,6.1,1.68,962,5.38,3.34,1.61,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\n896,PFTTQx,S365,4.4,4.4,0.9,7.4,0.59,22.6,10.8,2.09,1099,5.26,3.4,1.86,CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\n897,PFTTPz,S365,2.1,2.1,0.85,4.7,0.51,31.1,11.7,2.66,1097,5.21,3.53,1.68,CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\n898,PCzTTQx,S365,3.5,3.5,0.88,6.6,0.53,25.8,10.7,2.41,1114,5.23,3.33,1.9,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\n899,PCzTTPz,S365,3,3,0.75,6.4,0.54,46,16.6,2.77,1112,5.17,3.51,1.66,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\n900,PFDCN,S366,4.74,4.74,0.99,9.62,0.5,17.7,10.4,1.7,845,5.3,3.43,1.87,CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\n901,PFPDT,S366,4.37,4.37,0.99,9.61,0.46,16.3,10.2,1.6,980,5.26,3.5,1.76,CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\n902,P2,S367,0.48,0.48,0.8,1.45,0.41,205.7,59.2,3.48,815,5.51,2.53,2.34,CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\n903,P3,S367,1.33,1.33,0.9,4.33,0.34,162.4,48.3,3.36,684,5.51,2.54,2.14,CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\n904,CPDT-co-TPADCN,S368,1.14,1.14,0.64,4.45,0.4,22.9,9.4,2.44,857,5.08,3.38,1.7,CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\n905,CPDT-co-TPADTA,S368,1.18,1.18,0.62,4.65,0.41,9.8,5.5,1.79,991,5.06,3.37,1.69,CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\n906,CPDT-co-TPATCN,S368,0.22,0.22,0.58,1.26,0.32,11.5,6.9,1.66,882,5.06,3.72,1.34,CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\n907,CPDT-co-FADCN,S368,1.36,1.36,0.79,3.51,0.49,32.9,11.3,2.92,1370,5.2,3.4,1.8,CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\C%10=CC=C(/C=C(C#N)\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\n908,CPDT-co-FADTA,S368,1.38,1.38,0.7,4.57,0.43,10,4.4,2.26,1504,5.21,3.52,1.69,CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\n909,CPDT-co-FATCN,S368,0.31,0.31,0.7,1.17,0.38,15.6,6.8,2.3,1395,5.17,3.83,1.34,CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\C%10=CC=C(/C(C#N)=C(C#N)\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\n910,P1,S369,0.28,0.28,0.81,0.713,0.498,26.8,18.5,1.45,680,5.55,3.26,2.29,CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\n911,P2,S369,3.04,3.04,0.8,6.6,0.576,45.9,24.4,1.88,696,5.33,3.23,2.1,CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\n912,P3TDTQ,S370,0.56,0.56,0.67,1.82,0.46,12.3,8.4,1.46,1313,5.37,3.67,1.7,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\n913,P3SDTQ,S370,0.72,0.72,0.63,2.48,0.45,15.5,9.3,1.85,1457,5.35,3.72,1.63,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\n914,P3TDTDPP,S370,3.18,3.18,0.54,10.65,0.56,13.3,8.4,1.58,1079,5.21,3.94,1.27,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\n915,P3SDTDPP,S370,2.81,2.81,0.51,12.33,0.45,17.2,10.5,1.63,1222,5.16,3.91,1.25,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\n916,P(FBT-alt-Se2Th2),S371,7.34,7.34,0.7,15.8,0.664,20.3,14.7,1.38,1184,5.39,3.7,1.56,FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\n917,H12,S372,2.49,2.24,0.77,6.09,0.53,19.3,14,1.38,612,5.28,3.33,1.95,CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\n918,HEH,S372,1.39,1.18,0.8,4.04,0.43,20.8,12,1.73,500,5.27,3.31,1.96,CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\n919,F12,S372,3.04,2.86,0.84,5.93,0.61,23.2,16,1.45,648,5.4,3.45,1.95,CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\n920,FEH,S372,5.2,4.94,0.87,9.82,0.61,32.8,14,2.34,536,5.42,3.51,1.91,CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\n921,PGeTFDTBT,S373,5.47,5.47,0.71,13.51,0.57,103.6,37,2.8,1199,5.28,3.72,1.56,CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\n922,PGeDTBT,S373,3.51,3.51,0.66,7.46,0.68,97.5,39,2.5,1127,5.04,3.47,1.57,CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\n923,PK,S374,1.11,1.11,0.454,4.82,0.51,13.5,7.5,1.8,760,4.8,3.49,1.31,CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\n924,PE,S374,0.87,0.87,0.387,5.56,0.4,17,8,2.4,776,4.77,3.46,1.31,CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\n925,pDSBT-BT,S375,6.38,6.38,0.82,12.69,0.6,38,20,1.9,610,5.2,3.5,1.7,CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\n926,PDTSTTz-4,S376,5.88,5.88,0.73,11.25,0.716,9.3,6.3,1.47,918,5.04,3.41,1.76,CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\n927,PQS,S377,2.37,2.37,0.57,8.6,0.48,18.9,11,1.71,1742,5.2,3.47,1.73,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\n928,PQSQT,S377,2.22,2.22,0.44,9.77,0.51,22.3,11.2,1.99,1550,5.17,3.31,1.86,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\n929,DTS-C6,S378,4.12,4.06,0.9,8.96,0.51,29.4,19.5,1.51,826,5.33,3.52,1.63,CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\n930,DTS-T6,S378,2.7,2.55,0.98,6.01,0.46,27.9,19.1,1.46,832,5.33,3.39,1.72,CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\n931,BDT-C6,S378,0.45,0.44,0.83,1.81,0.3,44.3,18.6,2.38,854,5.4,3.5,1.86,O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\n932,BDT-T6,S378,0.73,0.72,0.87,2.64,0.33,66.4,18.8,3.53,860,5.41,3.45,1.92,O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\n933,PDTPTBT,S379,2.04,2.04,0.55,8.91,0.421,22.1,11.3,1.95,917,5.27,3.57,1.62,CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\n934,PDHTT,S380,4.2,4.01,0.716,8.54,0.66,12.9,8.6,1.5,444,5.15,3.19,1.96,CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\n935,PDOTT,S380,4.23,4.03,0.754,7.96,0.67,24,15,1.6,500,5.14,3.17,1.97,CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\n936,PDDTT,S380,3.53,3.23,0.771,6.42,0.65,39.6,22,1.8,612,5.17,3.18,1.99,CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\n937,PDTBTV,S381,0.46,0.46,0.43,3.15,0.335,36.9,7.9,4.67,610,5.01,3.03,1.69,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\n938,PDTBTFV,S381,1.24,1.24,0.83,4.32,0.346,43.7,9.8,4.46,646,5.2,3.14,1.79,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\n939,PTVcBBO,S382,0.01,0.01,0.35,0.12,0.26,13.4,5.6,2.4,658,5.19,3.02,2.17,CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\n940,PTVtBBO,S382,0.08,0.08,0.4,0.66,0.31,10.8,4,2.7,658,5.14,3.1,2.04,CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\n941,PEBT,S383,0.53,0.53,0.57,2.33,0.4,5.1,4.4,1.16,556,5.3,3.65,1.77,CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\n942,PEBTBT,S383,1.07,1.07,0.45,4.16,0.57,6.4,4.7,1.36,690,4.89,3.69,1.37,CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\n943,PEBTBTTBT,S383,1.04,1.04,0.6,4.41,0.4,5.7,3.9,1.47,854,4.95,3.39,1.57,CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\n944,PCzTh-TVCN,S384,1.33,1.33,0.99,3.72,0.361,59.5,16,3.72,830,5.57,3.39,2.18,CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\n945,PCzTh-TVDCN,S384,2.16,2.16,1.03,5.75,0.365,52.9,13.8,3.83,699,5.6,3.55,2.05,CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\n946,PCzTh-TVDT,S384,1.3,1.3,0.96,4.67,0.291,57.1,15.9,3.59,833,5.59,3.65,1.94,CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\n947,PQTDPP,S385,2.28,2.28,0.58,7.16,0.55,987,345,2.86,1217,5.19,3.64,1.36,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\n948,PQTVTDPP,S385,1.97,1.97,0.5,7.6,0.51,691,302,2.29,1243,5.05,3.66,1.33,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\n949,PBDTNTDO-1,S386,1.09,1.09,0.81,4.71,0.287,59.9,24.1,2.48,770,5.14,3.28,1.82,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\n950,PBDTNTDO-2,S386,1.52,1.52,0.88,5.67,0.305,40.1,13,3.07,742,5.19,3.3,1.83,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\n951,PBDTNTDO-C1,S387,1.96,1.96,0.87,4.42,0.508,11.1,6.3,1.7,942,5.19,3.38,1.81,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\n952,PBDTNTDO-C2,S387,1.01,1.01,0.71,4.21,0.34,17.2,3.9,4.3,814,5.23,3.33,1.8,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\n953,PBDTNTDO-C3,S387,2.21,2.21,0.81,4.93,0.552,53.4,21.9,2.4,798,5.27,3.39,1.79,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\n954,PBDTT-DPP,S388,6.6,6.5,0.73,14,0.65,89.5,40.7,2.2,1241,5.3,3.63,1.44,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\n955,PBDTP-DPP,S388,6.2,6,0.76,13.6,0.6,69,36.3,1.9,1229,5.35,3.56,1.46,CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\n956,PBDTT-FDPP,S388,5.8,5.5,0.77,13.8,0.55,63.4,28.8,2.2,1097,5.26,3.64,1.55,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\n957,PBDTP-FDPP,S388,3.3,3,0.77,7.42,0.59,41.8,20.9,2,1197,5.33,3.57,1.52,CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\n958,PT-Tz-DTBT,S389,2.63,2.63,0.76,7.75,0.45,41.1,22,1.87,1049,5.58,3.65,1.91,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\n959,PT-Tz-DTffBT,S389,4.42,4.42,0.88,10.11,0.5,83.9,36.6,2.29,1085,5.59,3.57,1.92,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\n960,PBdT-BTz,S390,2.81,2.81,0.88,5.2,0.613,31.3,20.2,1.55,972,5.16,2.82,2.01,CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\n961,PBdT-TTz,S390,3.4,3.4,0.9,5.5,0.687,17.2,11.3,1.52,946,5.19,2.9,1.91,CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\n962,PBdT-DTBT,S390,1.13,1.13,0.8,4.58,0.307,19.1,11.2,1.7,940,5.09,3.1,1.7,CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\n963,PBdT-DPP,S390,1.31,1.31,0.71,3.28,0.561,14.3,9.1,1.57,997,5.01,3.36,1.41,CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\n964,P1,S391,4.51,4.51,0.65,11.72,0.587,60.5,31.7,1.9,1320,5.34,3.7,1.64,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\n965,P2,S391,3.58,3.58,0.68,9.94,0.528,60,29.4,2.04,965,5.73,3.88,1.85,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\n966,PBDT-TTz,S392,3.32,3.32,0.92,6.21,0.58,149.5,56,2.67,943,5.42,3.58,1.85,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\n967,PBDT-TDPP-S,S393,4.89,4.89,0.84,10.04,0.56,17,13.4,1.27,1186,5.34,3.52,1.73,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\n968,PBDT-I,S394,1.53,1.53,0.84,3.9,0.46,168.3,33,5.1,1183,5.82,3.88,1.58,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\n969,PBDT-TIT,S394,4.22,4.22,0.79,7.87,0.68,109.2,42,2.6,1347,5.78,3.91,1.61,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\n970,PBDT-OIO,S394,1.39,1.39,0.73,3.15,0.6,243,90,2.7,1571,5.74,3.91,1.59,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\n971,PBDFTT-C,S395,4.4,4.4,0.66,10.45,0.638,44,21,2.1,706,5.27,3.69,1.48,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\n972,PBTT-BT (P1),S396,2.18,2.18,0.81,6.07,0.44,254.2,41,6.2,646,5.09,3.34,1.75,CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\n973,PBTTDPP,S397,0.8,0.78,0.67,2.79,0.43,19,11.5,1.65,1020,4.96,3.69,1.27,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\n974,PBTTTTz,S397,1.07,1.03,0.62,3.09,0.56,104.9,22.7,4.62,1395,5.15,3.52,1.63,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\n975,PBTTTPD,S397,0.78,0.75,0.79,2.64,0.37,35.7,14.9,2.4,817,5.41,3.61,1.8,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\n976,PBTTTzQx,S397,0.65,0.63,0.43,3.16,0.48,23.3,17.4,1.34,1737,4.8,3.6,1.2,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\n977,BTT-BTz,S398,5.06,5.06,0.81,10.9,0.57,42,23,1.8,947,5.65,3.6,2.05,CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\n978,PNB-3,S399,0.62,0.62,0.66,2.76,0.34,26.5,14.8,1.79,658,5.22,3.44,1.63,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\n979,PNB-4,S399,5.27,5.27,0.64,13.5,0.62,54.1,33.4,1.62,1103,5.14,3.54,1.64,CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\n980,PBDTTT-EFF,S400,5.28,5.28,0.693,11.77,0.648,10.5,5.7,1.85,886,5.19,3.64,1.55,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\n981,PBDTTT-EFT,S400,9,9,0.784,16.86,0.682,44.2,22,2.01,918,5.24,3.66,1.58,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\n982,PBDTTT-EFS,S400,8.78,8.78,0.807,16.57,0.656,160.8,69,2.33,1014,5.29,3.71,1.58,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\n983,PDBPTBT-2,S401,3.28,3.28,0.9,6.1,0.59,99.3,51.4,1.93,989,5.51,3.49,2.02,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\n984,PDBPTBT-3,S401,3.99,3.99,0.8,8.03,0.62,41.9,21.1,1.99,989,5.44,3.46,1.98,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\n985,PDBPTBT-4,S401,4.1,4.1,0.75,9.42,0.58,85.3,62.9,1.36,860,5.32,3.5,1.82,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\n986,PDBPTBT-5,S401,7.06,7.06,0.96,11.09,0.67,160,33.4,4.79,878,5.57,3.63,1.94,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\n987,P1,S402,4.35,4.35,0.81,9.96,0.538,30.9,17,1.82,1442,5.41,3.59,1.82,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\n988,P2,S402,7.93,7.93,0.82,15.1,0.642,128.2,58,2.21,1478,5.43,3.61,1.82,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\n989,P3,S402,7.43,7.43,1,13.25,0.556,57,38,1.5,1514,5.5,3.68,1.82,CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\n990,P0,S403,7.8,7.69,0.768,15.79,0.636,47.3,21,2.25,921,5.34,3.59,1.75,CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\n991,PBT,S404,1,0.96,0.57,4.23,0.4,52.2,24.7,2.1,1083,4.87,3.3,1.57,CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\n992,PFBT,S404,6,5.53,0.67,12.15,0.67,95.3,41.8,2.3,1101,4.91,3.35,1.56,CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\n993,PDFBT,S404,7.3,7.15,0.73,14.32,0.69,62.5,29.1,2.1,1119,5.11,3.52,1.59,CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\n994,P1-0,S405,7.25,7.04,0.8,13.38,0.68,91.1,41.1,2.24,504,5.56,3.83,1.73,CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\n995,PIDTT-TID,S406,6.7,6.7,1,12.6,0.53,131,35.4,3.7,1362,5.89,3.84,1.49,CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\n996,PBDD-ff4T,S407,9.2,8.8,0.95,13.2,0.73,80.2,56.9,1.41,1060,5.42,3.53,1.74,CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\n997,PBDPP-OD,S408,2.13,1.9,0.74,4.3,0.67,410.4,114,3.6,1465,5.27,3.86,1.41,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n998,PBDB-TT0,S409,7.28,7.16,0.886,11.75,0.699,49.1,15.3,3.21,1212,5.47,3.54,1.78,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\n999,PTB7-TV,S410,8.55,8.55,0.75,15.75,0.72,53.2,15.2,3.5,866,5.15,3.24,1.64,CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\n1000,PBDT-NQx,S411,5.3,5.09,0.8,11.03,0.601,53.2,38,1.4,1889,5.24,3.42,1.8,CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\n1001,PBDTS-NQx,S411,7.05,6.72,0.85,12.71,0.653,68,40,1.7,1953,5.31,3.46,1.81,CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\n1002,PDPPTT-2T,S412,6.1,6.1,0.6,15.8,0.64,205.9,106.7,1.93,1027,4.8,3.44,1.36,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\n1003,PDPPMT-2T,S412,6.5,6.5,0.62,15.8,0.66,229.4,138.8,1.65,873,4.8,3.46,1.34,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\n1004,PffBX4T-2OD,S413,9.4,9.1,0.875,15.8,0.66,189,102,1.86,1185,5.51,3.85,1.66,CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\n1005,PTBI2T,S414,5.6,5.6,1.05,8.2,0.66,183,76.2,2.4,1309,5.7,3.22,1.78,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\n1006,PTBI2TR,S414,8,7.1,1,10.9,0.65,984,65.2,15.09,1421,5.58,3.31,1.71,O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\n1007,PTBITT,S414,2.4,2.4,1.07,4.2,0.53,114,56.1,2.03,1283,5.85,3.4,1.73,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\n1008,PTBI2Tz,S414,0.05,0.05,0.4,0.34,0.32,517,114,4.54,1311,6.12,3.56,1.91,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\n1009,PBDTDTBT-H,S415,7.68,7.56,0.83,13.92,0.665,165,98.2,1.68,1057,5.03,3.3,1.73,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\n1010,PBDTDTBT-R,S415,8.22,8.12,0.84,13.64,0.717,282.2,120.1,2.35,1185,5.01,3.29,1.72,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\n1011,PBDTDTffBT-H,S415,9.44,9.34,0.88,14.92,0.719,127,63.2,2.01,1092,5.06,3.3,1.76,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\n1012,PBDTDTffBT-R,S415,9.09,9.01,0.88,13.98,0.739,153.3,71.3,2.15,1221,5.03,3.28,1.75,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\n1013,PBDTTT-H,S415,9.38,9.21,0.8,17.37,0.675,181.5,73.5,2.47,846,5.1,3.42,1.68,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\n1014,PBDTTT-R,S415,5.72,5.58,0.82,12.1,0.576,101.2,46.2,2.19,974,5.06,3.39,1.67,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\n1015,P1,S416,4.9,4.76,0.53,16.1,0.57,70.2,48.1,1.46,652,4.94,3.56,1.37,CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\n1016,P2,S416,6.88,6.72,0.6,18.04,0.65,86.3,56.8,1.52,670,5.13,3.76,1.37,CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\n1017,P3,S416,9.76,9.61,0.66,20.69,0.71,89.8,53.8,1.67,688,5.2,3.74,1.46,CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\n1018,P1,S417,4.11,4.08,0.65,10.58,0.593,188.5,23.3,8.08,1637,5.05,3.45,1.6,CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\n1019,P2,S417,5.73,5.66,0.73,12.87,0.602,87.7,22.6,3.89,1655,5.09,3.49,1.6,CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\n1020,P3,S417,8.26,8.17,0.82,14.41,0.7,106.7,25.2,4.24,1673,5.06,3.41,1.65,CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\n1021,PzIIG-BDT2TC8,S418,5.26,5.26,1.01,7.93,0.656,69.4,28.2,2.46,1419,5.48,3.64,1.63,CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\4=O)C=N3)=O)=C2C=C1\n1022,PzIIG-BTT2TC10,S418,3.36,3.36,0.94,5.89,0.608,51.2,23.5,2.18,1643,5.4,3.58,1.64,CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\4=O)C=N3)=O)=C2C=C1\n1023,PMOT5,S419,9.25,9.11,0.96,13.45,0.71,112.5,45.9,2.45,1272,5.28,3.22,1.83,CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\n1024,PBDTBDD,S419,6.77,6.65,0.84,12.45,0.65,75.6,30,2.52,1212,5.16,3.11,1.82,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\n1025,PMOT2,S419,8.01,7.91,0.88,13.18,0.69,52.7,27,1.95,1403,5.22,3.21,1.78,CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\n1026,PBQ-3,S419,6.48,6.32,0.81,11.73,0.68,47.9,23.5,2.04,1343,5.1,3.15,1.73,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\n1027,PBDTBO-CIBTDD,S420,9.11,9.01,0.76,16.79,0.717,113.8,36.7,3.1,1218,5.47,3.7,1.7,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\n1028,PBDTBO-CIBTEH,S420,6.88,6.51,0.79,13.33,0.631,88.5,32.9,2.69,1162,5.5,3.73,1.69,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\n1029,PBDTHD-CIBTEH,S420,5.46,5.29,0.78,10.94,0.644,58.6,21.8,2.69,1275,5.53,3.71,1.71,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\n1030,PBDTHD-CIBTDD,S420,4.95,4.72,0.68,11.69,0.623,38.9,17.5,2.23,1331,5.53,3.71,1.68,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\n1031,PBPD-Th,S421,8.4,8.2,0.95,12.4,0.71,107,42,2.55,1233,5.42,3.36,1.9,CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\n1032,PBPD-Se,S421,9.8,9.6,0.9,14.9,0.73,92,48,1.92,1328,5.35,3.31,1.77,CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\n1033,PBDTT-O-TT-CF,S422,8.68,8.68,0.78,16.5,0.68,34.6,19,1.82,920,5.31,3.33,1.52,CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\n1034,PBDTT-S-TT-CF,S422,9.58,9.58,0.89,15.1,0.71,51.8,27,1.92,952,5.44,3.31,1.56,CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\n1035,PIDTBDTID,S423,2.66,2.51,0.87,7.24,0.42,36.9,21.5,1.7,2229,5.47,3.72,1.75,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\n1036,PIDTBDT(ID)2,S423,2.5,2.33,0.93,6.34,0.423,13.3,11.7,1.1,3144,5.53,3.8,1.73,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\n1037,P1,S424,0.61,0.61,0.6,3.08,0.33,49.4,19,2.6,1100,5.26,2.86,2.4,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\n1038,P1,S425,3,2.9,0.6,7.83,0.609,35,24,1.46,1372,5.14,3.69,1.5,CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\n1039,P2,S425,2.28,2.2,0.6,6.99,0.588,20,14,1.43,1452,5.18,3.57,1.9,CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\n1040,PBDT-TSR,S426,10.2,9.91,0.804,17.79,0.706,63,30,2.1,1934,5.3,3.45,1.55,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\n1041,PDPP[T]2-EDOT,S427,2.6,2.5,0.32,15.5,0.5,383.4,142,2.7,917,5.73,3.66,1.13,CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\n1042,PDPP[Py]2-EDOT,S427,2.4,2.2,0.8,5.1,0.54,61.7,25.7,2.4,907,6.07,3.74,1.59,CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\n1043,PDPP[Ph]2-EDOT,S427,1.8,1.7,0.91,4.4,0.43,35.1,16.7,2.1,905,5.89,3.53,1.91,CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\n1044,PBDTA-INDI,S428,5.04,4.81,0.93,8.51,0.637,249,61.1,4,1463,5.41,3.29,2,CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\n1045,PBDTT-INDI,S428,6.35,6.26,0.96,10.26,0.645,165.9,48.3,3.4,1595,5.47,3.46,1.98,CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\n1046,P1,S429,1.43,1.33,0.85,2.79,0.6,39.9,16.3,2.5,1141,5.6,3.88,1.72,O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\n1047,P2,S429,9.26,9.13,0.87,14.91,0.71,154.5,42.2,3.7,1177,5.72,3.95,1.77,O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\n1048,PIDT-DTQ-T,S430,6.41,6.41,0.86,11.42,0.658,46.2,22,2.1,2253,5.33,3.29,1.63,CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\n1049,PIDT-DTQ-TT,S430,6.63,6.63,0.83,12.43,0.653,46,20,2.3,2309,5.29,3.27,1.6,CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\n1050,PBTF-OP,S431,9,8.9,0.86,16.4,0.622,134.6,64.3,2.09,938,5.45,3.34,1.62,CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\n1051,PCDPP,S432,9.02,9.02,0.86,16,0.65,705.8,136,5.19,1948,5.44,3.89,1.55,CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\n1052,PF0,S433,5.7,5.62,0.74,11.76,0.655,53.2,28,1.9,1465,5.29,3.58,1.71,CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\n1053,PF1,S433,6.29,6.13,0.8,11.85,0.662,35.2,22,1.6,1483,5.39,3.7,1.69,CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\n1054,PF2,S433,6.54,6.45,0.86,11.67,0.653,39.8,24,1.66,1501,5.48,3.73,1.75,CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\n1055,PIDTT-TT,S434,7.08,6.98,0.96,10.96,0.65,60.8,32.5,1.87,1184,5.35,3.11,2.14,CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\n1056,PIDTV-ffBT,S435,7.3,7,0.7,17.1,0.61,90.7,28,3.24,908,5.23,3.69,1.53,CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\n1057,PDFBC-DPP,S436,7.33,7.33,0.8,13.15,0.68,124.4,73.2,1.7,1379,5.35,3.82,1.53,CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\n1058,P-2T,S437,7.91,7.69,0.76,17.48,0.595,108.8,45.7,2.38,1365,5.27,3.1,1.63,FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\n1059,P-TT,S437,9.96,9.58,0.8,18.15,0.686,125.3,58,2.16,1339,5.3,3.13,1.62,FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\n1060,PBDTT-DTFPQx,S438,7.2,7,0.87,11.4,0.73,81,43.1,1.88,1343,5.52,3.86,1.66,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\n1061,PC1BT6,S439,7.34,7.21,0.95,14,0.552,134.4,42,3.2,1220,5.48,3.59,2.01,CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\n1062,PC2BT6,S439,6.62,6.46,0.99,13.11,0.51,34.7,20.4,1.7,1234,5.49,3.56,2,CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\n1063,PC6BT6,S439,6.39,6.21,0.98,12.91,0.505,47.3,27.8,1.7,1290,5.49,3.56,2.01,CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\n1064,PNC2C4BT6,S439,6.67,6.44,0.99,13.24,0.509,52.9,25.2,2.1,1122,5.48,3.63,2.01,CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\n1065,PC2BT,S439,4.02,3.94,1.01,10.48,0.38,19.7,11.6,1.7,1202,5.54,3.61,2,CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\n1066,PBDTT-BTAZT-1,S440,6.95,6.64,0.75,14.11,0.624,67.8,32.3,2.1,1211,5.11,3.12,1.65,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\n1067,PBDTT-BTAZT-2,S440,6.16,5.96,0.75,12.73,0.624,70.4,30.6,2.3,1195,5.13,3.14,1.62,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\n1068,PIDTI-BT,S441,4.02,4.02,0.82,8.99,0.546,46.3,26.9,1.72,2095,5.3,3.76,1.65,CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\n1069,PIDTI-DTBT,S441,3.72,3.72,0.8,9.07,0.514,122.3,76.9,1.59,2259,5.26,3.74,1.66,CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\n1070,h-PPDTNTz,S442,4.6,4.44,0.7,13.4,0.49,15.7,9.8,1.6,993,5.3,3.79,1.51,CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\n1071,d-PPDTNTz,S442,6.66,6.54,0.72,14,0.66,115,46,2.5,1217,5.38,3.76,1.62,CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\n1072,PDVF-8,S443,3.57,3.52,0.65,8.58,0.641,178,63.8,2.79,1047,5.19,3.63,1.56,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\n1073,PDVF-10,S443,4.56,4.49,0.65,10.56,0.666,86.1,26.4,3.26,1159,5.23,3.67,1.56,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\n1074,PtBTPBDT,S444,4.03,3.89,0.68,9.09,0.63,133,70,1.9,1149,5.29,3.83,1.46,CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\n1075,PtFBTPBDT,S444,3.11,3.07,0.83,5.79,0.64,106,53,2,1185,5.42,3.97,1.45,CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\n1076,PtBTPDPP,S444,0.94,0.91,0.6,2.47,0.61,131,61.9,2.1,1227,5.2,3.99,1.21,CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\4C=CC=C%10)=C3S1\n1077,PtFBTPDTS,S444,2.71,2.67,0.68,6.54,0.6,78,20,3.9,822,5.09,3.7,1.39,CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\n1078,PtBTPIDT,S444,3.64,3.46,0.77,10.01,0.45,48.7,35.1,1.39,1273,5.28,3.78,1.5,CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\4C=CC=C%15)=C3S1\n1079,PcBTPBDT,S444,1.23,1.19,0.66,3.4,0.53,70,27,2.6,1149,5.29,3.81,1.48,CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\n1080,P1,S445,6.21,6.13,0.84,11.74,0.63,39.2,13.5,2.9,917,5.44,3.84,1.5,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\n1081,PTSSO-TT,S446,3.79,3.79,0.71,11.86,0.45,27.4,15.1,1.8,850,5.4,3.8,1.56,CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\n1082,PTSSO-BDT,S446,1.93,1.93,0.72,7.78,0.35,63,26,2.4,1157,5.5,3.9,1.59,CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\n1083,PQx,S447,3.97,3.92,0.85,8.96,0.52,66.9,25.1,2.6,1675,5.4,3.58,1.82,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\n1084,PphQx,S447,5.03,4.98,0.8,10.85,0.58,66.1,23.2,2.6,1673,5.4,3.64,1.75,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\n1085,PBDT(ff)-ttTPD,S448,7.45,7.4,0.98,12.49,0.61,105.6,48,2.2,1554,5.65,3.49,1.91,CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\n1086,PBDTT-ttTPD,S448,6.79,6.65,0.84,12.07,0.67,90.3,43,2.1,1482,5.45,3.58,1.87,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\n1087,PBDTOT-FBT,S449,4.84,4.84,0.92,8.71,0.603,29.8,17.5,1.7,1228,5.46,3.55,1.79,CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\n1088,PBDTOT-BT,S449,2.47,2.47,0.88,7.6,0.369,24.8,13.8,1.8,1192,5.25,3.54,1.56,CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\n1089,PBDTOT-DPP,S449,3.05,3.05,0.78,8.29,0.472,29.2,10.7,2.73,1249,5.2,3.52,1.33,CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\n1090,PBDTBTz-T,S450,6.15,6.09,0.92,10.53,0.629,44,22.2,1.98,1413,4.95,2.82,1.89,CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\n1091,PBT-2TPF4,S451,5.7,5.59,0.854,10.93,0.606,12.4,10.1,1.23,1201,5.63,3.88,1.75,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\n1092,PffBT-2TPF4,S451,3.6,3.49,1.017,6.73,0.526,8.9,5.5,1.61,1237,5.84,4.07,1.77,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\n1093,PBDD4T,S452,6.53,6.24,0.86,11.16,0.68,29.4,12.2,2.41,1024,5.3,3.27,2.03,CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\n1094,PBDD4T-2F,S452,9.04,8.68,0.88,15.13,0.68,44,22.2,1.98,1060,5.39,3.61,1.78,CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\n1095,P(BT-DPP),S453,1.48,1.48,0.64,3.65,0.63,42.4,19,2.5,1165,5.17,3.55,1.32,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\n1096,P(BT-DPP)-T,S453,2.45,2.45,0.64,6.22,0.62,24.3,13.1,2.02,1165,5.22,3.52,1.34,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\n1097,PBDTfDTBO-L,S454,1.37,1.32,0.76,3.97,0.455,21.9,15.2,1.44,1337,5.51,3.56,2.01,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\n1098,PBDTfDTBT-L,S454,4.58,4.41,0.86,8.72,0.61,32.2,14.3,2.25,1353,5.44,3.54,1.98,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\n1099,PBDTfDTBS-L,S454,5.34,5.29,0.82,9.66,0.674,27.6,15.3,1.8,1400,5.4,3.55,1.92,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\n1100,P1,S455,5.06,4.98,1,8.76,0.58,85,34,2.5,1140,5.6,3.78,1.82,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\n1101,P2,S455,5,4.93,0.9,10.31,0.54,142.5,57,2.5,1196,5.54,3.77,1.77,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\n1102,P3,S455,7.13,7.06,0.92,12.21,0.64,149.6,44,3.4,1253,5.56,3.78,1.78,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\n1103,PFBDT-DTBT,S456,7.13,7.07,0.9,13.26,0.598,71.7,45.1,1.59,1293,5.41,3.6,1.71,CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\n1104,PFBDT-DTffBT,S456,7.33,7.15,0.96,13.24,0.577,62.2,57.1,1.09,1329,5.82,3.7,1.79,CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\n1105,P2-Ome,S457,2.92,2.92,0.76,7.59,0.506,114.6,67.4,1.7,1391,5.46,3.48,1.66,CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\n1106,PTZ6,S458,8.1,7.9,0.96,10.9,0.767,58.8,31.3,1.88,1353,5.36,3.36,2,CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\n1107,P1,S459,0.86,0.86,0.7,2.06,0.43,26.8,12.4,2.16,940,5.15,3.09,1.91,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\n1108,P2,S459,2.22,2.22,0.8,4.84,0.5,20.6,11.7,1.76,924,5.23,3.08,1.89,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\n1109,P3,S459,1.28,1.28,0.95,2.57,0.36,12.4,8.7,1.43,879,5.41,3.08,1.93,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\n1110,P4,S459,1.05,1.05,1,1.87,0.38,10.7,7.6,1.41,947,5.46,3.09,1.94,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\n1111,PThzTITI,S460,0.98,0.98,1.08,1.6,0.568,130.6,62.2,2.1,1045,5.64,2.78,2.05,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\n1112,PSezTITI,S460,2.36,2.36,1.05,3.75,0.596,305.4,85.8,3.56,1093,5.65,2.82,1.97,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\n1113,PVB1,S461,2.84,2.84,1,6.8,0.42,60,23.7,2.53,996,5.51,3.52,1.99,CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\n1114,PVB2,S461,2.05,2.05,1.09,5.33,0.35,51.9,28.5,1.82,869,5.64,3.54,2.1,CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\n1115,P(BDTT-BTBDPPD),S462,4.62,4.62,0.9,7.99,0.64,84.6,26,3.24,1987,5.44,3.34,2.1,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\n1116,PDTfBO-T,S463,5.63,5.56,0.93,11.1,0.543,53.2,31.3,1.7,1067,5.5,3.66,1.84,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\n1117,PDTfBO-DT,S463,5.61,5.49,0.89,10.3,0.61,75,37.5,2,1149,5.48,3.62,1.86,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\n1118,PDTfBO-TT,S463,5.6,5.35,0.87,9.69,0.664,50.9,31.8,1.6,1123,5.39,3.5,1.89,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\n1119,poly(DPP-alt-BP),S464,1.97,1.97,0.75,7.25,0.362,380.2,194,1.96,1153,5.5,3.82,1.64,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n1120,poly(DPP-alt-BT),S464,3.21,3.21,0.63,9.83,0.52,304.4,139,2.19,1165,5.27,3.94,1.33,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n1121,poly(DPP4T-alt-TBP),S464,4.54,4.54,0.71,10.08,0.633,304.5,150,2.03,2288,5.42,3.9,1.52,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n1122,PBDT-DTQ,S465,3.84,3.84,0.67,10.37,0.555,30,15,2,1925,5.19,3.29,1.54,CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\n1123,PIDT-DTQ,S465,6.41,6.41,0.86,11.42,0.658,46.2,22,2.1,2253,5.33,3.28,1.63,CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\n1124,P8,S466,6.73,6.73,0.73,14.76,0.621,74.3,42.2,1.76,894,5,3.46,1.54,CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\n1125,P9,S466,6.84,6.84,0.75,14.15,0.646,43.2,29.2,1.48,942,5.14,3.54,1.6,CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\n1126,r-PTTDPP50,S467,2.32,2.32,0.632,9.81,0.374,203.2,170.9,1.18,1149,5.16,3.89,1.47,CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\n1127,DT-PDPP2T-TT,S468,5.55,5.5,0.72,11.79,0.65,2535,780,3.25,1139,5.1,3.7,1.38,O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\n1128,PIIDBT,S469,4.58,4.58,0.87,8.51,0.619,139.2,45.8,3.04,1015,5.54,3.97,1.57,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\n1129,PIIDFBT,S469,6.21,6.21,1.01,9.11,0.672,198.1,75.9,2.61,1051,5.79,4.18,1.61,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\n1130,PHBCDPPC20,S470,2.12,2.12,0.92,6.53,0.353,24,13,1.9,1881,5.32,3.67,1.7,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\n1131,PHBCDPPC8,S470,2.85,2.85,0.86,10.38,0.318,69,12,5.6,1545,5.28,3.62,1.69,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\n1132,PHBCDPPF,S470,1.89,1.89,0.88,6.39,0.336,41,11,3.8,1849,5.3,3.61,1.73,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\n1133,PHBCDPPDT,S470,2.74,2.74,0.79,10.5,0.331,34,13,2.6,2045,5.19,3.63,1.64,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\n1134,P1,S471,6.56,6.56,0.86,11.92,0.64,39.2,13.5,2.9,917,5.44,3.84,1.5,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\n1135,P(BDTT-TTBDPPD),S472,5.37,5.21,0.9,8.94,0.67,169,0,3.67,1961,5.42,3.36,2.06,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\n1136,PA,S473,3.75,3.75,0.855,8.669,0.506,124,48.2,2.57,1072,5.76,3.94,1.82,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n1137,PB,S473,2.42,2.42,0.769,6.9,0.456,25.9,14.1,1.83,1100,5.66,3.85,1.81,CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\n1138,PC,S473,2.26,2.26,0.861,6.914,0.38,18.1,8.2,2.2,852,5.71,3.93,1.77,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\n1139,PHF,S474,7.2,6.95,0.84,12.46,0.69,137.7,52.7,2.61,1671,5.36,3.62,1.74,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\n1140,PFH,S474,6.19,5.96,0.93,9.57,0.7,87.4,54.9,1.59,1671,5.43,3.61,1.82,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\n1141,PFF,S474,2.9,2.79,0.92,4.61,0.68,139.8,63.2,2.21,1707,5.43,3.69,1.74,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\n1142,P,S475,7.54,7.42,0.65,16.12,0.72,23.9,9.7,2.46,1587,5.25,3.83,1.12,CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\n1143,P1,S476,7.27,7.27,0.9,12.62,0.64,20.2,10.4,1.94,1969,5.34,3.88,1.16,CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\n1144,P2,S476,6.68,6.68,0.92,11.72,0.62,13,8.3,1.57,1829,5.34,3.94,1.08,CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\n1145,PBDT-TPD,S477,1.92,1.92,0.46,10.5,0.392,38.9,25.9,1.5,869,5.53,3.46,1.84,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\n1146,PBDT-Th-TPD,S477,1.11,1.11,0.74,4.17,0.361,153.3,73,2.1,1033,5.41,3.42,2.17,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n1147,PBDT-TT-TPD,S477,1.36,1.36,0.74,4.88,0.372,16.8,12,1.4,1145,5.21,3.02,2.03,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\n1148,PDPP2TPCL,S478,4.7,4.7,0.77,9.5,0.64,240.2,72.8,3.3,1323,5.06,3.89,1.42,CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\n1149,PTTABT,S479,4.65,4.65,0.69,10.19,0.658,106.4,54,1.97,1228,5.3,3.12,1.64,CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\n1150,PTTABDT,S479,5.46,5.46,0.79,10.52,0.654,113.5,61.7,1.84,1247,5.33,3.03,1.77,CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\n1151,\"P4,9-BNDTDTFBT\",S480,7.23,7.23,0.88,11.56,0.71,47.1,24.5,1.9,1163,5.55,3.7,1.76,CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\n1152,\"P5,10-BNDTDTFBT\",S480,5.56,5.56,0.74,12.42,0.605,25.8,16.1,1.6,1163,5.49,3.61,1.74,CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\n1153,P(BDP-DTPz),S481,6.2,6.1,0.859,11.1,0.653,32.5,10.5,3.1,1173,5.27,3.75,1.8,CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\n1154,P1,S482,6.87,6.71,0.89,12.32,0.62,204.9,68.3,3,978,5.64,3.96,1.68,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\n1155,P2,S482,8.27,8.04,0.85,14.49,0.67,200.3,74.2,2.7,1007,5.53,3.87,1.65,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\n1156,P3,S482,7.84,7.7,0.84,13.89,0.67,217.8,77.8,2.8,1063,5.57,3.9,1.67,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\n1157,P4,S482,7.38,7.13,0.84,12.81,0.69,197.1,70.4,2.8,1119,5.57,3.89,1.67,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\n1158,P5,S482,6.28,6.05,0.86,10.61,0.69,275.2,86,3.2,1175,5.61,3.95,1.66,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\n1159,PBDT-DFQX-TTSEH,S483,7.02,6.71,0.85,12.58,0.661,169.4,45.9,3.69,1386,5.48,3.46,1.73,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\n1160,PBDT-DFQX-TTSC8,S483,8.51,8.37,0.85,14.63,0.682,116.9,40.3,2.9,1386,5.37,3.47,1.72,CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\n1161,P1,S484,2.71,2.71,0.86,5.96,0.53,19.6,12.4,1.58,1122,5.22,3.6,1.7,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\n1162,P2,S484,3.48,3.48,0.9,6.16,0.62,20.6,11.9,1.73,1254,5.34,3.6,1.7,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\n1163,PDPP-SS,S485,2.51,2.51,0.6,6.46,0.65,110.8,71,1.56,1261,5.25,3.97,1.28,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n1164,PDPP-TT,S485,3.43,3.43,0.64,7.26,0.73,304.4,139,2.19,1165,5.31,3.9,1.41,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\n1165,PBDPBT-T,S486,4.32,4.32,0.88,8.5,0.577,28.1,23.6,1.51,1028,5.31,3.48,1.83,CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\n1166,PBDPBT-TT,S486,2.13,2.13,0.8,5.6,0.476,27.9,9.6,2.91,1140,5.29,3.32,1.97,CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\n1167,PBDPBT-biT,S486,4.5,4.5,0.88,8.6,0.594,34.8,21.3,1.63,1192,5.35,3.5,1.85,CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\n1168,BTzDTBT,S487,2.92,2.92,0.51,10.31,0.56,47.5,19,2.5,1066,5.2,3.55,1.65,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\n1169,BTzDTFBT,S487,5.14,5.14,0.62,12.7,0.65,59.8,23,2.6,1084,5.3,3.65,1.65,CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\n1170,BTzDT2FBT,S487,7,7,0.75,14.64,0.64,94.5,27,3.5,1102,5.4,3.74,1.66,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\n1171,PDPPHT-TBT,S488,3.51,3.51,0.63,11.66,0.48,35.5,20.9,1.7,1217,5.24,3.66,1.48,CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\n1172,PDPPHT-BDTT,S488,2.46,2.46,0.77,7.26,0.44,25.7,14.3,1.8,1297,5.4,3.53,1.5,O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\n1173,PBBDTBT,S489,4.57,4.5,0.73,8.94,0.7,130,43,3,1437,5.43,3.67,1.76,CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\n1174,PBDTT-fDTBO,S490,2.88,2.75,1.05,5.53,0.496,123.8,88.4,1.4,1173,5.64,3.73,1.91,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\n1175,PBDTO-fDTBO,S490,2.8,2.75,1.02,5.41,0.507,172.3,89.3,1.93,1041,5.56,3.57,1.99,CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\n1176,TBFPF-BT,S491,6.8,6.8,0.8,12.12,0.71,53.4,38.5,1.38,1201,5.28,3.6,1.68,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\n1177,TBFPF-BO,S491,5.98,5.98,0.89,10.35,0.65,51.6,32.3,1.59,1185,5.38,3.69,1.69,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\n1178,P1,S492,4.36,4.36,0.58,12.98,0.583,21.7,12.5,1.74,1648,5.12,3.56,1.23,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\n1179,P2,S492,3.66,3.66,0.61,9.33,0.645,30.4,18,1.69,1519,5.14,3.58,1.28,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\n1180,P3,S492,0.45,0.45,0.62,1.6,0.451,35,24.3,1.44,1555,5.22,3.75,1.21,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\n1181,P4,S492,2.79,2.79,0.72,5.93,0.653,62.7,40.5,1.55,1484,5.24,3.64,1.22,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\n1182,PSB-DFBT,S493,1.88,1.8,0.76,6.39,0.39,58.3,30.2,1.93,1053,5.39,3.54,2.08,CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\n1183,PSB-DTDFBT,S493,0.48,0.41,0.58,2.97,0.28,83.6,40.2,2.08,1385,5.3,3.55,2.16,CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\n1184,PSB-FTT,S493,4.45,4.39,0.82,9.5,0.57,247.8,99.9,2.48,1195,5.21,3.41,1.97,CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\n1185,LGC-D013,S494,7.22,6.99,0.87,11.29,0.731,61.4,49.1,1.25,1715,5.56,3.72,1.84,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\n1186,TQF2-1,S495,4.6,4.6,0.93,8.5,0.58,64.4,26.9,2.4,684,6.18,3.7,1.8,CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\n1187,PTI-1,S495,3.7,3.7,0.88,6.8,0.62,127,44,2.9,821,5.78,3.95,1.6,CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\3)=O)C=C1\n1188,PR11,S495,4,4,0.92,7.6,0.57,90.7,34.9,2.6,1475,5.88,3.98,1.58,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\n1189,PIDTT-DTBO,S496,4.6,4.47,0.88,10.5,0.497,73.7,33.5,2.2,1505,5.36,3.69,1.69,CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\n1190,PIDTT-DTBT,S496,4.91,4.79,0.86,10.2,0.56,72.7,30.3,2.4,1521,5.31,3.67,1.72,CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\n1191,PTBTfBTzSi,S497,4.95,4.95,0.98,9.53,0.53,20.2,10.4,1.94,1182,5.38,3.67,1.53,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\n1192,PBDTS-FBT,S498,1.42,1.42,0.8,6.65,0.303,9.3,8.9,1.05,840,5.49,3.46,1.73,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\n1193,PBDTS-DTFBT,S498,3.19,3.19,0.83,8.27,0.464,34.5,25.2,1.37,1172,5.47,3.54,1.69,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\n1194,PBDT-TPD,S498,2.14,2.14,0.93,5.23,0.416,10.3,4.6,2.23,933,5.51,3.34,1.88,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\n1195,PBDTS-DPP,S498,2.41,2.41,0.78,7.79,0.396,10.9,6.7,1.62,1192,5.3,3.45,1.45,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\n1196,PDTTDPP-EH,S499,2.22,2.22,0.54,8,0.51,46.8,13,3.6,1247,5.11,3.69,1.42,CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\n1197,PDTTDPP-BO,S499,2.93,2.93,0.55,10.01,0.54,64.6,17,3.8,1359,5.16,3.77,1.39,CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\n1198,PTTIBT,S500,0.85,0.85,0.62,3.28,0.42,24,18,1.3,655,5.32,3.5,1.68,CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\n1199,PTTIMBI,S500,2.6,2.6,0.69,7.1,0.53,27,12,2.19,665,5.29,3.61,1.54,CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\n1200,pDSBT-BHTBT,S501,3.76,3.76,0.89,8.64,0.49,14.7,9.2,1.6,942,5.2,3.4,1.8,CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\n1201,P1,S502,1.51,1.44,0.87,3.77,0.46,25.1,13.7,1.83,1264,5.49,3.5,1.99,CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\n1202,P2,S502,3.33,3.21,0.86,7.48,0.52,21.4,12.6,1.69,1264,5.41,3.39,2.02,CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\n1203,BDT8TT,S503,1.63,1.63,0.77,4.5,0.473,49.4,26,1.9,988,5.76,3.51,1.33,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\n"
  },
  {
    "path": "dataset/NagasawaOPV/NagasawaOPV.json",
    "content": "[\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" PBTTT-C14\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 46.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 724\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 9.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 73.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 37\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 731\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 6.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" PCPDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 47.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 26.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 564\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 15.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" PffBT4T-2OD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 93.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 47.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1089\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 18.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" PffBT4T-2OD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 52.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 28.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1089\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 18.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" PffBT4T-2OD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 71.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 38.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1089\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 17.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" PffBT4T-2OD\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 29.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1089\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 16.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" PNTz4T-2OD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 49.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 30.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1161\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 19.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" PBDTTT-CF\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 68.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" -\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 756\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" -\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 7.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.669\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" PSBTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 21.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 580\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" PNTz4T\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 126.2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 52.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 1273\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 9.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 19.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1\\n\",\n        \"output\": \" 0.7340000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" PSEHTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 132.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 33.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 974\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 13.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C5=C6SC(C)=C5)=C6S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" PNOz4T\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 417.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 57.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 1241\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 7.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 14.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" P3HT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 21.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 196\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 15.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C)S1\\n\",\n        \"output\": \" 0.575\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" PQT-12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 694\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 4.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" PQT-12\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 47.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 694\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" PTB7-Th\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 124.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 72.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 7.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 7.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 14.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.691\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" PTB7-Th\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 78.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 7.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 7.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 13.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" PTB7-Th\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 249.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 40\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 12.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" PTB7-Th\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 375.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 48\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 11.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C)S6)C6=C4C7=CC=C(CC(CC)CCCC)S7)S3)=C2S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" PTB7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 97.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 46.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 786\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 14.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" PPDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 42.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 17.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 885\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" PPDTFBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 71.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 29.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 903\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 5.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" PPDT2FBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 119.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 42.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 921\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 7.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 7.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 11.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" PCz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 75.5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 39.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 531\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" PCV\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 425\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.889\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.46399999999999997\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" PCVT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 533\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1.0759999999999998\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.445\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" PCVTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 840\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.8590000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.484\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" PCVTTTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1003\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.7609999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.43200000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" PCPTDO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1061\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 1.558\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1\\n\",\n        \"output\": \" 0.546\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 54.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 36\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 731\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTQx\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 715\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTTPP\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 18.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 726\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTPT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 732\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTBX\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 51.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 26\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 725\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTPX\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 716\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 717\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4.15\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 727\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.73\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 952\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PC-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 24.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 16.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 787\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 7.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" TP3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 815\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" TP4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 939\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" PF-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 15.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 716\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" TP1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 744\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" TP2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 868\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 4.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" PIC-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 33.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 17.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1171\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" TP5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 20.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1199\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" TP6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 26.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 14.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1323\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 1309\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" PDPP3T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 170.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 54\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 859\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" PCBTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 63.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 956\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCC)CCCCCCCC)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" PCBTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 56.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 1068\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" PGFDTDPP (C4)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 37.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 890\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PGFDTDPP (C8)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 49.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 14\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1003\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" PGFDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 24.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 10\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 778\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" PC-DTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 161.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 91.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 1012\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" PF-DTDPP\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 27.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 15.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 941\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" PDTP-DTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 14.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 968\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 5.02\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 4.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" PDTP-DTDPP(Bu)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 38.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 18.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 855\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 14.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" PDPP-DTS\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 31.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 968\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 7.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC([Si](CC(CC)CCCC)(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.508\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" PDPP-BDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 20.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 997\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 8.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.44299999999999995\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" PDPP-BDP\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 47.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 22.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 965\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 4.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 4.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.627\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" P4TDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 19.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 1104\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 8.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" P4TBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 19.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 12.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 716\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 4.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" P4TDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 26.2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 880\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 6.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" P4TPDTQ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 26.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 13.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 1283\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" PCTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 38.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 953\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 10.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" PTB1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 22.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 18.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 824\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 15.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PBDTTT-C\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 30.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 16.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 738\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 14.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" PDTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 128.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 35.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 1089\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 9.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" PBDTDPT1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 157.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 43.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 1022\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 6.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" PBDTDPT2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 600.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 91.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 910\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 6.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 4.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 4.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 10.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH]\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 89.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 882\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 4.85\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 7.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 110.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 55\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 882\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 300.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 64\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 749\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 8.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" PDTSTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 44.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 709\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C4=C5SC(C)=C4)=C5S3)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" H3\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 147.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 67.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 612\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" H6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 84.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 46.7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 668\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" H8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 55.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 29.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 726\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 4.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" H1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 40.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 866\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 4.78\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" H7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 31.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 18.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 720\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" H9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 76.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 34.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 720\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 4.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" H11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 35.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 16.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 768\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" PBDT-BT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 468.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 112\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 908\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 9.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 9.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 15.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDTPTD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 34.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 13.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" PBDTBDD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 1212\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 6.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 6.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 10.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10\\n\",\n        \"output\": \" 0.723\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" PBQ-4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 54.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 22.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1379\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 8.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 8.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 13.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.7020000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" PBQ-1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 210.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 68.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1307\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 4.66\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 5.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 5.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 12.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.701\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" PBQ-2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1343\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 4.86\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 6.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 6.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 13.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.633\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" PBQ-3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 65.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 18.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1343\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 4.92\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 7.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 7.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.677\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" PBDTTT-S-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 684.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 108.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1032\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 12.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" PDT-S-T\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 114.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 22.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 1144\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 7.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 7.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 16.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1\\n\",\n        \"output\": \" 0.6409999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" PBDTDTTT-S-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 125.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 35.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 1196\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 7.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 7.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 16.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9\\n\",\n        \"output\": \" 0.6629999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" PBDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 201.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 54.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 833\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 0.423\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" PBDTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 353.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 82.2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 996\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 13.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.691\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" PBDPP-1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 100.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 40\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 1221\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" PBDPP-2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 60.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 1353\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 8.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" PBDPP-3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 48.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1465\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 6.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 6.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 16.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" PBDTFQ-T\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 270.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 101\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1291\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 9.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" PBDTFQ-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 15\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1403\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 10.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 1233\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 6.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 88.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 42.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 1181\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 167.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 19.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 1238\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 51.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 1482\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 7.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 7.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 13.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" PTB1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 22.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 18.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 824\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 12.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.654\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" PTB2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 768\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 12.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.6629999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PTB5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 22.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 16.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 768\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.431\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PTB6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 25.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 16.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 824\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 7.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" PTB3\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 23.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 15.9\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 736\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 13.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC\\n\",\n        \"output\": \" 0.568\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" PTB4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 19.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 14.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 786\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 13.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.614\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" PBDT-TS1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 99.3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 30.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 982\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 9.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 9.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 17.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 0.672\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" PBDT-TS2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 28.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 16.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 982\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 8.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 8.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 16.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7\\n\",\n        \"output\": \" 0.623\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" PBDT-TS3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 218.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 70\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 1038\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 7.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 7.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 16.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDTTPD-P1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 105.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDTTPD-P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 117.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 765\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDTTPD-P3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 94.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 35\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" PBDT-T8-TPD\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 79.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 37.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 869\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 6.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 6.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 9.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" PBDT-T10-TPD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 66.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 36.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 925\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 4.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 4.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 8.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" PBDT-T12-TPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 78.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 49.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 981\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 8.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.532\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" PBDTDTBT-p\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 53.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 28\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1128\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 9.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" PBDTDTBT-o\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 42.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 25\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1128\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 11.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" PBDTDTBT-m\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 32.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1128\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 10.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" PTBF0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 768\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 14.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC\\n\",\n        \"output\": \" 0.624\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" PTBF1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 97.5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 46.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 786\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.603\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" PTBF2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 26.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 804\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.42200000000000004\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" PTBF3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 78.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 822\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.39399999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBT-0F\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 61.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 18.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1204\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.667\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBT-1F\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 129.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 44.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1194\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 14.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.657\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBT-2F\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 31.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 12.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1212\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 14.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.677\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBT-3F\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 76.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1230\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.7240000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" PBnDT-HTAZ\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 122.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 47.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 1032\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 11.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 0.552\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" PBnDT-FTAZ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 99.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 42.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 1068\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 6.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 11.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 0.7290000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDFDTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 965\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 11.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.546\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDFDODTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 997\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDFDTBTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 18.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 835\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.575\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDFDTBO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 32.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 981\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" PBDTT-BT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 32.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 1072\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 5.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" PBDTF-BT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 22.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 1040\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 8.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 0.40299999999999997\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" PBDFT-BT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 1040\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 9.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9\\n\",\n        \"output\": \" 0.609\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" PBDFF-BT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 13.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 1008\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 5.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9\\n\",\n        \"output\": \" 0.556\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDFFBT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1095\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.584\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDTFBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1127\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDTBO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 254.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 62\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1012\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.644\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDTDTBTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 18.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 867\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.11\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBDTTDTBO\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 70.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 41.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1113\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 11.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.613\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBDTTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 25.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 16.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1129\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 10.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBDTTDTBTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 967\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 9.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.606\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" PBDT?DTBSe\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 42.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 20.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 1157\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 13.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell average value of PCE of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" PBDT?DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell average value of PCE at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 46.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell average value of PCE of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell average value of PCE of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 1109\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell average value of PCE at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell average value of PCE of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell average value of PCE of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell average value of PCE of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 11.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" PBDT-T-FBSe\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 59.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 27.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1419\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PIDT-T-FBSe\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 57.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 32.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1129\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 14.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.45899999999999996\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" PBPT-12\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 63.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 22.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 1242\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 12.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9\\n\",\n        \"output\": \" 0.542\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" PBDTTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 49.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 27.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1128\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9\\n\",\n        \"output\": \" 0.575\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" PBDTP-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 64.4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 32.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 1117\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 8.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 8.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 12.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9\\n\",\n        \"output\": \" 0.7090000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" PBDTPO-DTBO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 27.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1165\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 11.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" PBDTPO-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 25.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1181\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" PBDTPO-FBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1279\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 7.23\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9\\n\",\n        \"output\": \" 0.47100000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" PBDTTBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 268.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 62.5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1144\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 12.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" PBDTPBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 285.1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 64.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 1133\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" PBDTFBO\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 284.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 60.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 1113\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" PTBFTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 142.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 42.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1144\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 6.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 6.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 13.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" DTffBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 82.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 39.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 1141\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 7.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 7.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC\\n\",\n        \"output\": \" 0.621\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 104.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 52.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1105\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 4.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 4.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.47600000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" DTfBT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 74.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 39.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1123\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC\\n\",\n        \"output\": \" 0.522\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" PTBDTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 71.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 27.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 1225\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 8.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.5539999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" PTBDTffDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 34.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 996\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 12.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" PTBDTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 32.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 19.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 960\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 6.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBDT_TEH-DT_H-BTff\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 29.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 14.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1164\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 4.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 11.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.552\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" PBDT_TEH-DT_EH-BTff\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 33.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 22.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1164\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 13.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.619\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" PBDT_TEH-HDO_H-BTff\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 49.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 27.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 1201\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 15.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC\\n\",\n        \"output\": \" 0.6920000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" PBnDT-FTAZ\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 99.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 42.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 1068\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 6.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 6.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 11.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC\\n\",\n        \"output\": \" 0.7290000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" PFBT-BDT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 13.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 997\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" P(BDT-T-BT)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 22.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 1028\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 9.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" P(BDT-TT-BT)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 65.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 32.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1477\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 4.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 4.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 11.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" P(BDT-TT-BO)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 59.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 21.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1461\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 7.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 7.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 13.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.6659999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" P(BDT-TT-HBT)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 73.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 23.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1389\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 4.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 4.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 10.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell PDI of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" P(BDT-TT-FBT)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 47.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 16.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1425\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" PBDTT?DTTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 31.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 14.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 1549\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 6.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 6.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 12.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" PBDTT?DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 56.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1465\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 5.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 0.495\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" PBDT?TBT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 20.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1160\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.518\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" PBDT?TTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 16.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1385\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 11.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.6659999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-10HD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 60.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1367\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-10OD\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 35.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-12HD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 29.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1423\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-12OD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 65.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1535\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-14HD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 290.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 9.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-14OD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 130.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 44\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1591\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-EHOD\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1110.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 43\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1423\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-BOBO\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 37.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1311\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-BOHD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 110.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 35\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1423\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell weight-averaged molecular weight as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 11.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-BOOD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 47.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 28\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1535\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-14HD\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 18.0\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-14HD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 60.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-14HD\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 300.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 9.09\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-14HD\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1450.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 19.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" PTzBT-14HD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 18.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" PTzQT-14\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 27.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 1283\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" PTzBT-HD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 16.0\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 754\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" PDPP-BBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 872\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" TDPP-BBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 19.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 884\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 6.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" PBTPyDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 22.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 1043\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 5.77\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 7.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1\\n\",\n        \"output\": \" 0.6579999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" PDPP3T\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 400.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 147\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 859\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 15.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" PDPPTPT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 143.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 72\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 853\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" PDPP3TaltTPT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 154.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1681\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 15.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" C3-DPPTTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 154.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 80\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1139\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 23.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" C3-DPPTTSe\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 238.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1187\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 21.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" C3-DPPTTTe\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 272.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1237\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 21.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" PDPP2FT-C12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 78.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 46\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 714\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" PDPP2FT-C14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 92.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 771\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 14.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" PDPP2FT-C16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 87.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 55\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 827\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" PBDTT-FDPP\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 77.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 35.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1209\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" PBDTT-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 88.7\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 40.3\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1241\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 13.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" PBDTT-SeDPP\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 79.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 38\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1336\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" PDPP2TBP\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 176.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1041\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" F1-PDPP2TBP\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 277.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 67.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1077\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 4.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" F2-PDPP2TBP\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 142.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 72\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1077\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" PDPPTNT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 91.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 63.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 1015\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" DT-PDPPTPT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 215.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 89.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1077\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" DT-PDPP3T\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 457.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 136.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1083\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" DT-PDPP2T-DBT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 552.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 149.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1183\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" DT-PDPP4T\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 640.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 218.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1165\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 16.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" reg-PDPP/TPDalt2T\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 137.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 50\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1330\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 5.78\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 9.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" DTS-D-C\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 21.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 15.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1133\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" DTS-Ch\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 764\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" DTS-Chy\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 776\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)/CCCCCC)=O)=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" DTS-T-Ch\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 23.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 928\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(CCCCCC)(CCCCCC)C(C2=C(C)SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C(C)S7)S6)=C21)=O\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" DTS-T-Chy\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 19.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 7.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 940\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 5.02\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C(C(S2)=CC=C2C3=CC([Si]4(CC(CC)CCCC)CC(CC)CCCC)=C(S3)C5=C4C=C(C6=CC=C(C)S6)S5)SC(C)=C1C/7=O)C7=C(CCCCCC)/CCCCCC\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" DTS-T6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 27.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 19.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 832\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 6.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" BDT-C6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 44.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 18.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 854\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" BDT-T6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 66.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 18.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 860\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" DTS-C4\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 83.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 41.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 770\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCC)C(CCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell maximum value of PCE of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" DTS-Ceh\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 90.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 53.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 882\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 9.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CC(CCCC)CC)C(CC(CCCC)CC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" DTS-C8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 92.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 46.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 882\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" DTS-C6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 72.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 42.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 826\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 7.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 7.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 14.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)=C6)=C6[Si]2(CC(CC)CCCC)C[C@@H](CC)CCCC)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" BTI-BDT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 71.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 21.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 875\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 4.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 4.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 9.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 0.518\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" BTI-BDT(2)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 100.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 1044\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 9.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" \\u00ef\\u00bf\\u00bds\\u00ef\\u00bf\\u00bds1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 32.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 18.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1385\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)=C8S2)S1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" TT2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 127.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 36.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1885\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 8.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" BT1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 142.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 67.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 1435\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 6.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" BT2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 231.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 59.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 1935\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 10.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\\\\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" IP1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 88.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 40.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 970\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" IP2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 926\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" IP3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 23.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 915\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" IsoC6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 207.0\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 80\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1153\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" IsoC8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 146.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 70\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1209\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" IsoC10\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 126.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 61\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1265\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" IsoC12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 125.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 65\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1321\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" IsoC12\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 103.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1321\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 11.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" Iso2EH\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 126.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 53\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1209\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.81\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" PNDTI-T\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 26.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 1161\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" PNDTI-TT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 48.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 1217\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" PNDTI-DTT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 68.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 28.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 1273\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 9.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" PNDTI-BT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 90.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 27.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 1243\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" PBDTT-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 132.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 95\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 7.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 7.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 14.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.639\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" PBDTT-O-TT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 118.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 950\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 7.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 15.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.644\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" PBDTT-S-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 172.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 118\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 982\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 8.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 8.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 15.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.655\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" PBDT-TS1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 64.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 29.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 982\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 9.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 9.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 17.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7\\n\",\n        \"output\": \" 0.6609999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" PBTz4T\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 114.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 36.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 1053\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" PNNT12HD\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 88.9\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 1459\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 15.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" PNNT12DT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 139.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 46.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 1683\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" PNNTDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 310.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 1347\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 10\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" PNDT3BTz-DT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 54.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 30.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 1239\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 8.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" PNDT3NTz-DT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 310.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 1347\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 10\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" PNTz4TF2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1520.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 66.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1309\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 22.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 19.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" PNTz4TF4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 34.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 15.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1345\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" PBDT-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 130.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 40.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1409\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 0.34600000000000003\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" PBDT-DTNT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 59.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 24.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 1517\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 11.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" PTzNTz-EHBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 64.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 32.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1301\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 16.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" PTzNTz-EHHD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 91.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 47\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1413\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 15.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" PTzNTz-BOBO\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 113.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 51.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1413\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" PTzNTz-BOHD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 59.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 29.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1525\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" PF-C12NT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 69.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 23.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1325\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 6.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 6.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 12.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.614\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" PAF-C12NT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 59.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1505\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 8.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.625\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" PCz-C12NT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 84.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 21.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1340\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 4.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 4.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 11.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1\\n\",\n        \"output\": \" 0.564\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" PBDT-C12NT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 69.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 22.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 1849\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 10.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9\\n\",\n        \"output\": \" 0.685\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" PN1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 32.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 14.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 1257\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 8.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1\\n\",\n        \"output\": \" 0.37799999999999995\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" PIDT-EHNT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 42.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 19.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 1677\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" PIDT-DTNT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 35.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 17.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 1621\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 8.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" PIDT-C12NT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 43.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 17.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 1953\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 10.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" NT812\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 118.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 56.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 1135\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 10.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 10.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 19.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 0.7290000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" NT1014\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 165.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 59.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 1247\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 7.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1\\n\",\n        \"output\": \" 0.529\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" P\\u00ef\\u00bf\\u00bd\\u00ef\\u00bf\\u00bdNDTDTNT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 86.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 67.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 1459\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 8.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 8.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 15.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 0.644\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" P\\u00ef\\u00bf\\u00bd\\u00ef\\u00bf\\u00bdNDTDTNT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 60.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 28.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 1459\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 8.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104\\n\",\n        \"output\": \" 0.535\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" poly(CR-TPA)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 15.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 611\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 6.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" poly(NTD-TPA)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 627\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 6.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" BTT-TP\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 16.4\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1372\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 0.993\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 0.764\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 0.46799999999999997\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" BTT-FT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 24.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1407\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 0.919\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" BTT-NTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 62.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 39.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 2091\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 2.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 2.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 0.755\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 5.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11\\n\",\n        \"output\": \" 0.605\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" PDCBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 40.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 24.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 782\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 11.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" rr-PTB7-Th\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 89.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 35.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 1807\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 7.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 6.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 15.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 0.583\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" rr-PTBS\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 103.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 40.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 1871\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 10.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 10.19\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 19.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1\\n\",\n        \"output\": \" 0.633\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" P3TI\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 211.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1209\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 5.82\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 13.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\\\\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" O-PBDT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 32.3\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 474\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" SO-PBDT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 27.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 950\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 3.11\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" S-PBDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 61.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 16.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 506\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 7.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" PBDTT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 49.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 18.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 606\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 6.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 6.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 11.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" P3HDTTT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 18.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 500\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 6.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" PT-C1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 350\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1\\n\",\n        \"output\": \" 0.392\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" PT-C2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 432\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1\\n\",\n        \"output\": \" 0.484\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" PT-C3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 113.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 69.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 544\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 7.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.584\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" P3HST\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 28.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 15\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 228\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SCCCCCC)=C(C)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" P3HST-co-Th\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 81.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 310\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" C6-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 444\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" PBTDN\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 9.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 658\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" PBTADN\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 65.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 44.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 683\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1\\n\",\n        \"output\": \" 0.514\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" POPT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 17.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 300\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" POPTT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 19.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 14\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 464\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 6.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" POPQT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 546\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 8.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 556\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 6.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 150.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 664\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 23.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 689\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 11.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-3MT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 92.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 26.4\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 614\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 4.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 4.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" PBDT-BT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 28.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 975\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 5.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.45799999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" PBDT-BTC\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 39.8\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1025\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.414\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" PBDT-BTCox\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 66.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 37.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1057\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.584\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT[2F]T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 25.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 592\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT[2H]T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 33.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 15.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 556\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" PBTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 793\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 8.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" PDTTTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 11.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 931\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 8.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" PBTTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 103.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 50\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 920\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" PTTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 95.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1002\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 10.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" PTTTPD-C8C8 (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 110.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 44\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1002\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 4.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" PTTTPD-C8 (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 52.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 875\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" PTTTPD-EG (P3)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 20.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 851\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 4.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" PTTSPD-C8C8 (P4)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 81.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 1050\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" PTTFPD-C8C8 (P5)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 55.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 986\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" PTTFPD-C8 (P6)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 70.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 860\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 6.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" PTSTPD-C8C8 (P7)\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 71.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 36\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 1050\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 3.82\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 4.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 8.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" PTSTPD-C8C8 (P8)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 85.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 1098\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 4.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 7.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" PSBTSPD-C8 (P9)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 45.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 757\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 3.82\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 7.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 7.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 13.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" P(PTQD-Th)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 37.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 19.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 701\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 5.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 10.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" P(PTQD-2Th)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 38.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 18.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 783\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 11.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" PPDT1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 89.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 49.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 847\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.45299999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" PPDT2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 75.2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 41.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 843\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 4.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 4.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 9.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.521\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" PPDT3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 55.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 32.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 979\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.706\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" PPDT4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 45.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 30.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 735\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.316\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" PPDT5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 30.5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 819\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 8.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CCCCCCCC)CCCCCCCC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.405\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" PSOxTT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 48.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 24.3\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 1006\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 7.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(OCCCCCCCC)=C(C5=NC(SC(C6=C(OCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" PSOTT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 35.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 15.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 974\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C=C(S3)C4=CC(CCCCCCCC)=C(C5=NC(SC(C6=C(CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" PSEHTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 133.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 33.9\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 974\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(C[C@H](CC)CCCC)C[C@H](CC)CCCC)=C(S1)C3=C2C=C(S3)C4=CC(C[C@@H](CCCC)CC)=C(C5=NC(SC(C6=C(CC(CCCC)CC)C=C(C)S6)=N7)=C7S5)S4\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" PBDT-BDTP (P1)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 156.8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 49\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 1445\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 10.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9\\n\",\n        \"output\": \" 0.547\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" PS-BDTP (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 180.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 62.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 1131\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 6.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 6.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 9.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 0.745\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" PDTPO-BDTO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 291.1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 97.7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 960\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 6.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 6.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.706\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" PDTPO-BDTT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 188.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 75.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1092\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 6.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 6.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1\\n\",\n        \"output\": \" 0.705\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" PThBDTP\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 264.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 89.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 1083\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 9.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 8.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 12.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7\\n\",\n        \"output\": \" 0.755\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" PFTTz\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 93.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 36\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 613\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" PCTTz\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 111.8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 43\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 628\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" PBTTz\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 12.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 10\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 725\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 4.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" PIFTBT6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 63.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 26.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 916\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" PIFTBT10\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 21.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 1141\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" PIFDTQ10\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 45.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 22.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 1289\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 7.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" P3FTBT6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 24.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 14.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 1249\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" PITBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 25.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 640\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 5.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 5.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 12.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 0.502\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" PITFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 43.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 27.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 658\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 9.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 9.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 15.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1\\n\",\n        \"output\": \" 0.659\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" HXS-1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 51.4\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 861\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" PCDTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 24.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 860\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 5.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 4.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" PCDTTPD-ic\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 24.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1085\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" PCDTTPD-C6C8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 973\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" PCTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 36.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 973\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 5.72\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" PCTTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 40.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 12.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 1085\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" PCBTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 65.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 1137\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 7.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" PTTDBC-PhQC8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 1308\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 7.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" PTTDBC-BTC12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 29.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 14.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 1274\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 8.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" PC1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 1118\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 5.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 0.441\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" PC2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 44.8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 23.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 1178\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 7.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 7.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 12.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3\\n\",\n        \"output\": \" 0.5870000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" PC3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 23.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 14.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 1262\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 6.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 6.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 11.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3\\n\",\n        \"output\": \" 0.633\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" HD-PDFC-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 98.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 38.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 1010\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 7.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 7.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 14.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1\\n\",\n        \"output\": \" 0.563\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" PAn-BTBT (P1)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 185.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 57\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 1425\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" PAn-BTBT (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 152.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 1571\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" PTP27-DBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 1129\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" PTP36-DBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 1129\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1\\n\",\n        \"output\": \" 0.268\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" PPhIBDT-C12 (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 28.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 1008\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1\\n\",\n        \"output\": \" 0.547\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" PPhIBDT-ThEH (P3)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 43.4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 15.5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 1027\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 7.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1\\n\",\n        \"output\": \" 0.586\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" PBEHTT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 48.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 25.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 963\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 5.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" PTTEHV\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 584\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 5.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" PCEHTT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 962\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" PBTOTT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 284.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 103\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 946\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" PCPEHTT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 958\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 9.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" PBTOxTT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 150.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 56.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 978\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 4.91\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" PPEHTT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 8.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 959\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 4.91\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" PDEHTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 44.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 19.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 1115\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 5.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 10.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" POAPPO-BDT (Pa)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 76.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 31.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 1321\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 4.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 4.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 8.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2\\n\",\n        \"output\": \" 0.602\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" POAPPO-BDT (Pb)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 52.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 24.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 1321\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 0.462\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" POAPPO-BDT (Pc)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 45.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 22.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 1321\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2\\n\",\n        \"output\": \" 0.596\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" PBDTTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 48.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 10.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" PNDTTPD (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 90.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 914\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 11.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" PBDTTPD (P2)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 170.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 70\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 864\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 8.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" PBDTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 75.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.5379999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" PBDTT-LTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 36.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 15.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 1383\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 7.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 7.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 14.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" PTAC-TPD (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 113.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 20.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 1574\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" PBDT(F)TPD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 34.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 14.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 837\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 4.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" PBDT(T)TPD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 51.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 16.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 869\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" PBDT(S)TPD\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 40.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 965\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 4.98\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" PBDT-TZNT (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 122.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 48.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1315\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 7.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" PBDT-TZNT (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 116.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 74.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1539\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 7.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 7.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 11.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" PBDT-TZNT (P3)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 101.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 53.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1539\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" PBDTFBZO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 106.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 48.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 1036\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 6.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 6.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 11.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1\\n\",\n        \"output\": \" 0.5820000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" PBDTFBZS\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 75.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 39.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1068\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 7.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 7.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 12.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.7120000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" FTAZ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 149.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 81\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1068\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 8.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.759\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" PrzTAZ\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 78.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 53\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1034\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 4.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 4.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 8.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.597\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" PBnDT?PyCNTAZ\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 200.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1058\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 7.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 7.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.965\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 10.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.7140000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" CNTAZ\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 173.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 75\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1082\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 8.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1\\n\",\n        \"output\": \" 0.599\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" PTFBDT-BZS\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 223.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 66.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 1333\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 8.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 8.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 12.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" PTFBDT-BZO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 255.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 1317\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 9.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" PTZBIBDT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 56.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 22.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 1180\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 8.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 8.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" PV-BDTC1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 91.9\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 31.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 1251\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1\\n\",\n        \"output\": \" 0.594\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PV-BDTC2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 59.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 35.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1383\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 7.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 10.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDTBDD (PM6)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 38.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 19.3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1248\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" PBDT-HBTA\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 81.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 31.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 1224\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 5.13\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 7.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 0.565\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" PBDT-FBTA\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 43.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 32\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 1260\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 11.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1\\n\",\n        \"output\": \" 0.672\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDT(O)-T1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 52.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 27.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1244\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 4.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.495\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDT(S)-T1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 66.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 23.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1276\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 7.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.711\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDT(Se)-T1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 82.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 39.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1372\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 8.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 8.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 13.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.721\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDT(S)-T1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 77.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 48.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1276\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.6759999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" POBDT(S)-T1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 66.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 23.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1336\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 12.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.722\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDT-O1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 22.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1196\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDT-ST1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 34.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1212\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 13.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.747\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" PBDT-Se1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 27.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 17.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1260\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 13.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1\\n\",\n        \"output\": \" 0.747\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" PDBT-T1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 342.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 195.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 1324\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 9.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 9.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 14.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" PBT1-MP\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 24.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1388\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 12.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 0.725\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" PBT1-EH\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 25.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1388\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 14.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" PBT1-BO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 35.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 16.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1388\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 13.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1\\n\",\n        \"output\": \" 0.675\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" PIDT-SO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 133.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 72\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 1149\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 6.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" PIDT-DHTSO\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 73.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 45.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 1481\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPTI (P1)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 124.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 30.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1245\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.636\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" PSB-TPTI (P3)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 21.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 1217\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 7.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 0.5489999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" PSB-TPTI (P4)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 20.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 992\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 10.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6\\n\",\n        \"output\": \" 0.42200000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" PBDTTTP\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 277.2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 69.3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 1469\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 8.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6\\n\",\n        \"output\": \" 0.695\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" PSBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 9.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1375\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 11.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.496\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" PSBO\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 13.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1415\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.401\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" PSDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1651\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1\\n\",\n        \"output\": \" 0.413\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" PThTITI\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 289.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 106.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 1045\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 8.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 0.698\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" PSeTITI\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 318.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 88.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 1093\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 6.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 6.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 9.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3\\n\",\n        \"output\": \" 0.705\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" PThTD1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 335.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 58.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 1057\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 5.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 6.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 5.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 9.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 0.716\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" PThTD2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 146.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 33.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 944\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 6.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 11.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" PSeTD1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 253.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 70.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 1105\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 6.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 5.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 10.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O\\n\",\n        \"output\": \" 0.687\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" PSeTD2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 93.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 35.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 992\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 8.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 7.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 13.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O\\n\",\n        \"output\": \" 0.711\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" PzNDTT-TPD1\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 56.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 24.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 1532\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 7.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 7.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 12.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" PzNDTT-TPD2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 32.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 24.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 1532\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 6.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" PDTPO-IDTT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 41.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 23.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 1420\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 9.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" PDTPO-IDT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 68.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 30.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 1532\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 7.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 10.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" PIDT-OHBPz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 105.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 70.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1437\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.5660000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" PIDT-OFBPz\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 156.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 104.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1473\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 5.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 5.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 8.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" PIDT-OBPQ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 117.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 78\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1438\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 8.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.509\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" P-PDT-IID12OD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 37.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 26.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1639\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 4.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 9.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" P-PDT-IID12DT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 20.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1751\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 6.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" P-PDT-IIDBOBO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 106.1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 56.9\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1415\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" P-PDT-IIDHDHD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 28.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1639\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\\\\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" PTPTDP\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 51.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 28.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 1539\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" PBDT_TEH-TBTT_EHi (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 33.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 7.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1313\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 4.64\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 17.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.631\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" PBDT_TEH-TBTT_HDo (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 22.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1313\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 4.63\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 4.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 4.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 15.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.486\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell PCE. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" PBDT_TEH-TBT_HD (P3)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 22.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1426\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 4.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 7.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 7.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.633\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 18.15\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.652\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" BFR2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 66.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 926\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 7.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1\\n\",\n        \"output\": \" 0.606\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" BFS3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 74.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 34\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 1823\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 5.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 10.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 0.608\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" BFS4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 73.6\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 32\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 1655\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 7.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 7.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 13.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 0.603\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" BFS4b\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 128.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 1655\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 7.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 14.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11\\n\",\n        \"output\": \" 0.611\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" PBDTTT-E\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 92.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 768\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 4.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 4.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 11.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.547\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" PBDTTT-E-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 71.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 900\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 14.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.626\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" PBDTTT-C\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 77.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 738\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 6.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 6.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 15.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.5920000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" PBDTTT-C-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 64.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 870\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 7.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 7.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 17.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1\\n\",\n        \"output\": \" 0.5870000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" PBDTBT (Z3)\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 30.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 940\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 6.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.369\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" PBDTBT (Z4)\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 23.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 19.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 972\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.606\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" PDST-BDD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 91.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 53\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 1396\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 5.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 5.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 10.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 0.551\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" PBDT-BDD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 1212\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 6.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 6.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 10.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5\\n\",\n        \"output\": \" 0.723\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" PDST-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 33.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 1102\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 10.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" PDST-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 220.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 1537\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 4.01\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 6.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9\\n\",\n        \"output\": \" 0.541\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" PBT-S\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 40.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 14.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 1296\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9\\n\",\n        \"output\": \" 0.703\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" PBT-SO2-M\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 48.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 14.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 1360\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 5.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 0.379\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" PBT-SO2-H\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 35.7\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 14.3\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 1360\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 6.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 6.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 14.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9\\n\",\n        \"output\": \" 0.629\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" PBT-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 128.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 44.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1208\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 13.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.677\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" PBT-OP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 74.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 30.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 1229\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 7.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 7.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9\\n\",\n        \"output\": \" 0.718\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" PBDT-Tz-TPD (P1)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 110.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 26.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 927\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" PBDT-Tz-DPP (P2)\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 76.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 17.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1187\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" PBDT-Tz-TT (P3)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 133.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 25.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 1014\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" PTTBDT-FTT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 61.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 25\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 1030\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 7.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 7.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 14.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" PBT-TVT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 121.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 19.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 1198\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 6.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 8.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 8.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 16.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1\\n\",\n        \"output\": \" 0.627\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" PBDTBzT-DTffBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 40.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 1377\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 7.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 12.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10\\n\",\n        \"output\": \" 0.627\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" PBDTT-DTffBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 28.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1164\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 9.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9\\n\",\n        \"output\": \" 0.579\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" PTOBDTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 154.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 72\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 1601\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 6.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 11.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10\\n\",\n        \"output\": \" 0.6509999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" PQ1\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 61.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 34.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1627\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 0.507\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" PQ2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 82.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 33.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1629\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 7.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10\\n\",\n        \"output\": \" 0.621\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" PQ3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 68.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 48.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1905\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 0.524\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" PQ4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 51.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 32.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1885\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 6.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11\\n\",\n        \"output\": \" 0.488\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" PBDT2FBT-T1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 49.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 28.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1277\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 9.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.597\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" PBDT2FBT-T2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 48.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 42.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 1441\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10\\n\",\n        \"output\": \" 0.547\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" PBDT2FBT-T3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 102.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 48.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 1605\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 6.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 6.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11\\n\",\n        \"output\": \" 0.614\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" PBDT2FBT-T4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 109.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 33.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 1769\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 6.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12\\n\",\n        \"output\": \" 0.405\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" PTIPS-BDT-TT (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 20.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 872\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 12.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" PTIPS-BDT-TT (P3)\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 18.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 890\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 4.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 4.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 9.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" PTIPS-BDT-TT (P2)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 41.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 842\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 8.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" PBDTTT-S\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 18.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 10\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 788\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 6.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 6.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 14.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" PTB2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 768\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 14.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1\\n\",\n        \"output\": \" 0.624\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" PTB7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 97.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 46.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 786\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 14.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" PTBF2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 26.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 804\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1\\n\",\n        \"output\": \" 0.42200000000000004\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" PBB3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 181.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 91.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 1287\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 6.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" PBDT-CPDTO (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 32.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 21.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 790\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 4.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" PSB-CPDTO (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 762\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" PCz-CPDTO (P3)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 87.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 24.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 749\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 5.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" PFL-CPDTO (P4)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 28.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 17.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 734\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 5.92\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" PBnDT-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 70.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 41.2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1105\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 10.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.573\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" PBnDT-DTffBT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 87.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 33.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1141\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 12.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.612\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PBDT-DODTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 25.7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1028\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 8.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PTG1\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 51.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1048\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" P(BDT-TBTF)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 29.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1140\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 13.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.534\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PTG1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 52.5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1048\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.502\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PBDT-TPA (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1127\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 9.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PBDT-TPA (P2)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 12.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1434\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PDPAT-BDT-BT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 109.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 25.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1051\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 7.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.498\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" PBDT-OBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 40.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 19.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1144\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 12.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.5489999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" PBDT-FBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 58.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 22.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1259\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 6.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 12.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.599\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" PBnDT-FTAZ\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 34.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 18.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1082\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.544\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" PBnDT-FTAZ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 76.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 36.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1082\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 11.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.642\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" PBnDT-FTAZ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 119.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 55.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1082\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.705\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" PBnDT-FTAZ\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 156.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 71.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 1082\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1\\n\",\n        \"output\": \" 0.633\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" PNDT-DTPyT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 36.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 17.1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 1016\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 6.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 14.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 0.617\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" PQDT-DTPyT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 49.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 21.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 1017\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 13.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5\\n\",\n        \"output\": \" 0.551\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" PBnDT-DTPyT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 380.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 104.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 1106\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 6.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 6.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 12.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5\\n\",\n        \"output\": \" 0.5820000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" PTIPSBDT-DFDTBTz\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 50.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1134\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 6.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" PTIPSBDT-DTBTz\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 57.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 23\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1098\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 12.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" PBDT-DTBTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 40.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 15\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 7.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" PBDFNTDO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 18.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 766\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 4.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 4.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 9.14\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.5920000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" PBDTPF-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 32.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 13.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 1297\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 7.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 13.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" BDT-BT-2T\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 128.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 47.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1241\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" BDT-FBT-2T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 136.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 65.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1277\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" BDT-BT-2Fu\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 56.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 25.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1209\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 7.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" BDT-FBT-2Fu\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 79.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 34.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1245\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" PBDT-ffBT (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 40.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 22.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1221\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" PBDT-BT (P2)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 81.5\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 28.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1349\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 7.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" PBDT-TffBT (P3)\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 58.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 20.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1384\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 7.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" PBDT2FBT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 32.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 18.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 1305\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 7.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 0.519\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" PBDT2FBT-O\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 44.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 24.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 1309\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 4.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 4.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 7.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1\\n\",\n        \"output\": \" 0.647\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDT2FBT-T\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 27.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 21.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 1277\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 6.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 6.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.578\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDT2FBT-T-O\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 29.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 17.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 1309\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 7.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.528\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PSeB1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 15.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 864\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.602\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 15.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" PSeB2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 41.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 15.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 960\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 6.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 6.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" PSeB3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 52.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 28.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 864\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 6.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 5.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 0.635\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 14.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTTTBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 246.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 60.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1144\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTTTBS\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 157.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 45.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1208\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTTTBO\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 221.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 56.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1256\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 11.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" PBDTSTBO\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 275.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 67.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1256\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 7.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 13.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTTSBS\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 119.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 38.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1304\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" PBDTSTBS\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 160.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 47.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1304\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 11.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" PBDTSSBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 197.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 52.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1352\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" PBDTSSBS\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 87.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 31.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1400\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 31.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 17.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1164\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 10.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.536\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTBSe\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 39.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 24.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1212\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.506\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PBDT-DFBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 74.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 36.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 981\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.647\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTT-DFBO\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 58.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 29.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1113\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.586\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" PBDTF-DFBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 86.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 38.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 1081\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" PinBDFID\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 76.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 33.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 1731\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.737\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.486\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" PoutBDFID\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 33.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 17.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 1731\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.6409999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 1.306\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 92.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 37\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.888\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 65.3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 27.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 733\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 1.005\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 100.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 40.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 787\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 0.792\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 28.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 52.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 20.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P3)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 35.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 16.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 793\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P5)\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 12.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 901\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P7)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 369.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 131\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1126\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P8)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 37.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 957\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P9)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 19.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1126\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P10)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 94.4\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 41.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1182\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBDT-TPD (P11)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 52.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 22.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1182\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.73\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" TPO(CO)(2EH/C1)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 42.4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 799\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" TPO(CO)(2EH/C3)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 55.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 15.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 827\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" TPO(CO)(2EH/C7)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 74.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 20.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 883\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" TPO(CO)(2EH/C11)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 94.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 27.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 939\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" TPO(CO)(2EH/C13)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 78.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 26.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 967\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" TPD(2EH/C8)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 51.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 16.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 869\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 34.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 18.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1033\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.45299999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTTPD-HT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 23.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 14.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1202\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 6.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 6.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 10.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.604\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" INDT-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 49.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 15.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 1177\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 4.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 6.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" PBDTBT (P1)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 179.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 40.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1185\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" PBDTTPD (P2)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 72.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1286\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 36.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1217\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 7.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 7.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 13.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 0.5589999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 32.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 24.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1345\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1\\n\",\n        \"output\": \" 0.341\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTT-DTTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 41.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1202\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 8.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" PBDTTVT-DTTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 58.1\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 25.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 1418\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 6.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 52.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 834\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 6.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" P2a\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 41.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 787\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" P2b\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 168.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 40\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 787\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 5.63\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 7.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" P2c\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 180.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 787\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 8.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 161.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 35\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 787\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" POBDTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 43.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 25.1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 793\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PEBDTPO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 56.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 39.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 793\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PBDTTID\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 52.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 20.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1176\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PID1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 34.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 773\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 7.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.547\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PID2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 32.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 773\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.586\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PPB1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 37.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 18.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.97\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.6659999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PPB2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 27.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 8.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.622\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBTCT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 28.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 740\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBTCTO\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 24.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 608\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 8.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBTPDO\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 25.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 664\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 10.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBTFDO\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 22.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 660\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" PBT8PT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 60.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 23\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 813\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 6.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 12.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" PTP8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 26.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 12.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 945\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 6.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 6.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 11.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 0.585\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" PTN8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 44.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 20.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 930\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 8.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8\\n\",\n        \"output\": \" 0.41700000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 39.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 776\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 4.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 748\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 6.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(C(SC(CCCCCC)=C2)=C2C3=O)=O)C3=C(S1)C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CCCC)CC)CC(CC)CCCC)S4\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" PBDF-T1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 32.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 23.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 1169\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 4.74\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 9.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 8.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 13.49\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1\\n\",\n        \"output\": \" 0.755\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" PBDT-T1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 56.2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 26.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 1201\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 8.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 13.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1\\n\",\n        \"output\": \" 0.718\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" P(T-QX)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 34.3\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 648\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1\\n\",\n        \"output\": \" 0.659\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" P(BDT-Qx)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 660.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 1011\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 17.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5\\n\",\n        \"output\": \" 0.503\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" P(BDT-DTQx)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 78.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 12.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1175\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 0.552\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" PTIPSBDT-DTQX\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 80.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1279\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 4.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" PTIPSBDT-DFDTQX\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1315\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 6.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 6.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 10.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" PBDT-PTQ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 1307\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 4.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 4.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 12.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" PBDT-PTTQ\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 1695\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 10.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" PBDT-TQ\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 25.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 22.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 1098\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 4.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 8.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" PBDT-TTQ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 85.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 71.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 1318\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" PBDT-DTQx\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 38.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 19.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 1161\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 11.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" PBDT-TFQ\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 71.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 46.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 1154\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 17.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F\\n\",\n        \"output\": \" 0.5760000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" PBDTDTQx-O\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 186.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 84\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 1175\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2\\n\",\n        \"output\": \" 0.615\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" PBDTDTQx-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 80.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 49.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 1307\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 10.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2\\n\",\n        \"output\": \" 0.643\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" PBDT-DTQx\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 14.6\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 1010\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 11.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" PBDTDT(Qx-2)-O\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 23.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 11.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 1235\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 4.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 4.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 9.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" PBDTDT(Qx-2)-T\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 19.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 1367\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 6.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 6.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 10.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9\\n\",\n        \"output\": \" 0.614\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" PBDTDT(Qx-3)-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 97.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1307\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 11.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.647\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" P0F\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 88.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 32.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1162\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 4.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.8320000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 6.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" P1F\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 89.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 27.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1180\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.872\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 6.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" P2F\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 101.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 33.4\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1198\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.914\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 6.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" PBDT-DFQX-PP\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 43.2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 20.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 1363\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 8.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 0.514\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" PBDT-DFQX-TP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 63.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 40.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 1343\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 6.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 6.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 12.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9\\n\",\n        \"output\": \" 0.601\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" PBDT-DFQX-PT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 40.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 24.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 1343\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 6.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 6.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 12.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 0.635\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" PBDT-DFQX-TT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 81.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 44.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 1322\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 7.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 7.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 12.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9\\n\",\n        \"output\": \" 0.6990000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" PFQBDT-TR1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 64.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 25\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1343\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 5.89\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" PFQBDT-T2R2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 66.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1455\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 5.87\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" PBDTTFTQ-EH\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 181.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 64.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1325\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 7.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 7.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 13.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.708\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" PBDTTFTQ-DO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 250.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 1304\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 7.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 7.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 11.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 0.759\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" PBDTTFTTQ-EH\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 101.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 18.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1549\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 6.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 6.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9\\n\",\n        \"output\": \" 0.708\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" PBDTTFTTQ-DO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 863.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 136\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 1529\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 6.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 7.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 7.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9\\n\",\n        \"output\": \" 0.757\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" PTTPPz-BDT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 191.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 57.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 1253\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 9.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7\\n\",\n        \"output\": \" 0.5820000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" PTTPPz-BDTT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 71.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 24.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 1385\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 4.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 4.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9\\n\",\n        \"output\": \" 0.625\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" PBDT-PQD1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 283.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 113.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 1712\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 5.97\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" PBDT-PQD2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 354.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 98.4\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 1488\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 5.96\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" PBDT-PQD3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 573.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 179.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 1356\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 5.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" PT-PQD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 132.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 30.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 993\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 5.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" O-HD\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 91.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 42.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1189\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 9.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" BO-BO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 82.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 33.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 1189\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" PU-O\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 54.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 27.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1189\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" PBDT-DPP (P1)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 130.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 40\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1221\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 4.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 4.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 11.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.602\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" PBDT-DPP (P2)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 320.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 93\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1189\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 12.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.524\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" PBDT-DPP (P3)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 72.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 32\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1189\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 8.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.45299999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" PBDT-DPP (P4)\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 730.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 130\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 1241\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1\\n\",\n        \"output\": \" 0.32899999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" PTIPSBDT?DPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 190.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 76\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1437\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 7.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 16.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C(C)S6)N7CC(CCCCCCCC)CCCCCCCCCC)C7=O)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" PBDTF-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 141.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 26.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 1097\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 10.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1\\n\",\n        \"output\": \" 0.489\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" PBDTF-DPPF\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 169.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 30.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 1065\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 12.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1\\n\",\n        \"output\": \" 0.565\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" PBDT-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 152.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 28.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 997\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" PBDT-DPPF\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 154.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 29.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 965\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 8.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1\\n\",\n        \"output\": \" 0.5329999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 58.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 30.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 1353\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 6.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1\\n\",\n        \"output\": \" 0.369\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 49.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 28.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 1453\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1\\n\",\n        \"output\": \" 0.581\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" PBDTBPA(H)-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 71.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" -\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 1349\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" -\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 13.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" PBDTBPA(F)-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 24.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" -\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 1421\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" -\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 9.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" PBDTDPPcbp\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 72.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 1463\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 4.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 0.44799999999999995\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" PCBTDPPcbp\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 70.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 28.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 1422\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 4.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1\\n\",\n        \"output\": \" 0.319\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" PDPP2TzBDT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 326.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 85.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1191\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" PDPP2Tz2T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 196.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 108.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1167\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" PDPP2TzDTP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 274.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 88.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 955\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" PffBT-T4-2HD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 25.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 13.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 976\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 14.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.644\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" PffBT-T3(1,3)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 56.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 37.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 894\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 0.45299999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" PffBT-T3((1,2)-1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 129.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 72.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 1759\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 18.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 0.6409999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" PffBT-T3(1,2)-2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 109.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 66.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 1731\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 18.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9\\n\",\n        \"output\": \" 0.6829999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" PffBT-T2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 98.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 58.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 1539\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1\\n\",\n        \"output\": \" 0.486\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" EC12-DT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 69.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1799\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 6.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 5.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.861\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.575\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" EC12-OD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 98.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 58\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1687\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.873\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 7.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.564\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" EHD-HD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 48.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 34\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1687\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.9309999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.629\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" EHD-BO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 66.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 51\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1575\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.8109999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.491\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" EBO-BO\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 33.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 25\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1463\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.8340000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 8.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" PT-ID1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 36.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 17.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 933\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" PTT-ID1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 127.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 37.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 989\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" PBDT-ID\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 32.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 21.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 959\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 7.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" PBDT?IBTI\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 115.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 43.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 1485\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 11.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" PMIM\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 42.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 20.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 931\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 5.93\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 6.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" PT-MIM\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 24.1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1013\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 5.78\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 10.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell PCE. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" PBDTO-MIM\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 190.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 63.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1375\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 5.87\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 4.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" PBDTA-MIM\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 277.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 69.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1483\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 5.94\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" PBDT-ID\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 165.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 1183\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 5.81\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\\\\6)=O)C=C4\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" PBDT-TIT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 109.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 1347\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 5.75\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 4.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 4.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 4.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 9.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\\\\7)=O)C=C5)S4)S3\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" PBDT-BTI\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 181.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 55\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 1735\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 7.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 7.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 14.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" PBDT-TTI\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 625.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 139\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 2123\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 11.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" PBDT-IIG\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 54.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 1591\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 5.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 5.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 10.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O\\n\",\n        \"output\": \" 0.6579999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" PBDT-TIIG\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 95.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 1603\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 4.96\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 11.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O\\n\",\n        \"output\": \" 0.5720000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" PBDTT?ID\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 88.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 36.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 1479\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 8.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" PBDTT?FID\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 98.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 37.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 1515\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 7.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 7.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 70.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 23.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 698\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 54.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 27.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 867\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 65.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 29.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 666\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 56.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 22.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 1335\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" syn-PBDFID\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 343.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 146.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 1007\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 5.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" anti-PBDFID\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 88.7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 34.8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 1007\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 55.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 28.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 1401\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 44.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 19.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1569\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 24.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 1433\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1601\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" PBDFTT-C\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 69.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 40.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 706\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 4.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 4.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 13.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" PBDFTT-EF\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 103.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 61\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 754\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 15.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.5379999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" PBDFTT-CF\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 108.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 45.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 724\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 13.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.598\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" PBDFTT-S\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 48.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 37.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 756\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 14.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.607\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" PBDFTT-ECN\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 39.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 761\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 5.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1\\n\",\n        \"output\": \" 0.446\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" PBDFTT-CF-O\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 724\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 4.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 13.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1\\n\",\n        \"output\": \" 0.597\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" PBDFTT-CF-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 856\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 6.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 6.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 13.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1\\n\",\n        \"output\": \" 0.616\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 73.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 1000\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 6.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 86.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 33.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 968\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 6.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 206.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 50.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 968\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 4.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 7.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 337.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 66.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 937\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 12.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" BDF(2EH/C7)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 26.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 691\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 10.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" BDF(2EH/C8)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 40.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 705\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" BDF(2EH/C9)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 34.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 719\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" BDF(2EH/C10)\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 36.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 733\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" BDT(2EH/C8)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 49.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 14.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 737\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 12.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" P9\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 14.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 1443\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 4.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 4.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 9.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C4=NC(SC(C5=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S5)=N6)=C6S4)S3)O7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C)O1\\n\",\n        \"output\": \" 0.5870000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 68.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 24.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 1517\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 2.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 203.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 75.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 1535\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 4.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 4.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 8.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1\\n\",\n        \"output\": \" 0.612\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" PTDBD2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 108.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 38.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 978\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 13.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" PTDBD3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 105.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 45.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 1063\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2\\n\",\n        \"output\": \" 0.521\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" PTR5b\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 76.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 35.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 1066\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" PTR7a\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 19.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 1317\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" PTR7b\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 18.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 1429\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6\\n\",\n        \"output\": \" 0.28800000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" PTR9a\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 28.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 1679\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 7.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 0.546\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" PTR9b\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 41.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 14.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 1791\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" pDTBDT-TTEH\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 80.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 37\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 1319\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 6.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 15.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2\\n\",\n        \"output\": \" 0.594\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" pDTBDT-DTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 1374\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 6.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2\\n\",\n        \"output\": \" 0.539\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" PBT-HD-DPP-C16\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 1557\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 5.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2\\n\",\n        \"output\": \" 0.609\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" PBT-T-DPP-C12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 34.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 20.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 1689\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 12.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 0.634\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" PBT-TIPS-DPP-C16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 27.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 16.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 1437\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 6.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 6.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 13.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3C#C[Si](C(C)C)(C(C)C)C(C)C)S2\\n\",\n        \"output\": \" 0.613\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" PDPPBDT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 683.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 122\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1445\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.741\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" PDPPDTT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 64.5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 43\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1195\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 6.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 13.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" PDPPDTBDT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 75.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 1553\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 4.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 4.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 0.745\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" PDTBDT-ID\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 25.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 14.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 1295\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 12.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2\\n\",\n        \"output\": \" 0.503\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" PDTBDT-DTNT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 62.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 26.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 1629\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 7.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 7.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 17.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" PDTP-DTBDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 85.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 46.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 1677\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 6.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 6.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 15.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2\\n\",\n        \"output\": \" 0.5429999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" P(Ge-DTBT)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 97.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1127\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 7.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" P(Ge-DTCNBT)\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 109.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1152\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 6.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 6.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 14.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" P(Ge-CTDCNBT)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 44.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 20.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1177\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" TBTIT-h\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 546.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 151\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 1269\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 17.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" TBTIT-i\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 91.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 1269\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\\\\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" F-BT2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 134.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 34.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 1953\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" BT2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 231.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 59.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 1935\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 10.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\\\\8=O)=O)=C6)S5)S4)=N%11)=C%11C=C3S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" BTSA5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 66.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 14.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 855\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O\\n\",\n        \"output\": \" 0.682\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" P-PDTz-Tdt-HH\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 16.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 1391\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 4.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" TTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 110.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 859\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 4.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 10.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1\\n\",\n        \"output\": \" 0.5479999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" TPT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 24.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 853\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 4.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 12.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.39899999999999997\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" TTfT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 17.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 895\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" TPfT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 19.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 889\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 6.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O\\n\",\n        \"output\": \" 0.449\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" P[T-iI(HD)]-4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 54.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 26\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 821\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\\\\4C=CC(C)=C5)=O)C3=C2)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" P[T3(C6)-iI(HD)]-2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 66.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 1153\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" P[T3(C6)-iI(SiO)]\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 70.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 32\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 1313\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CCCCCC[Si](C)(O[Si](C)(C)C)O[Si](C)(C)C)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CCCCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)C)C7=C/6C=CC(C)=C7)=O\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" PDTBDT-BZ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 28.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 1189\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 10.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 0.649\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" PDTBDT-BZF\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 70.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 1207\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 7.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 11.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 0.735\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" PDTBDT-BZF2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 89.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 1225\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 10.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1\\n\",\n        \"output\": \" 0.605\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" DP3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 37.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1213\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 2.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.674\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 7.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.573\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" DP4\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 88.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 53.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1101\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.6970000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 8.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.643\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" PTF1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 18.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 1106\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 4.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 4.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" POF1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 85.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 974\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" PTF2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 54.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 21.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 1142\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" POF2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 75.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 19.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 1010\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 4.78\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" MBDT1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 125.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 53.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 1151\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 4.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 4.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 10.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" MBDT2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 124.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 35.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 1371\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" PBTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 77.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 44.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 583\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 10.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" PTVTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 57.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 609\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 7.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 6.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 12.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" PBBTz-Cz\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 1012\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" BTT-DTFFBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 1169\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 11.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" PBBTZBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 107.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 51\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 1693\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 0.8009999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 12.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 0.674\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" PCPDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 28\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 564\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.456\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" PCPDTFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 36.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 23.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 582\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 15.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" a-PTPTBT-SA\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 60.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 24.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 1069\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 0.672\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PBTISi-C6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 95.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 763\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.825\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 12.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.606\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PBTISi-C8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 93.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 791\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.8029999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 12.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.623\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PBTISi-EH\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 72.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 791\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.8340000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 12.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.531\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PBTIGe-C6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 78.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 809\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.774\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 11.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.502\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PBTIGe-C8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 67.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 25\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 837\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.745\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 11.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.47200000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PBTIGe-EH\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 41.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 837\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.769\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 9.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.467\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PTPDSi-C8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 52.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 709\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.885\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 11.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.649\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PGeBTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 98.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 626\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.78\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 18.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" P-Si\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 52.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 709\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Si]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" P-Ge\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 81.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 48\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 755\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PGe1-C8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 16.9\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 626\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PGe1-EH\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 21.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 12.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 626\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" PGe2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 31.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 16.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 755\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PSDTTT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 44.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 13.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1559\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=NC(SC(C4=CC5=C(C(SC(C6=CC7=C(C(OCC(CCCC)CCCCCC)=C(C=C(C)S8)C8=C7OCC(CCCCCC)CCCC)S6)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)=N%10)=C%10S3)=C%11)=C%11[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" PzNDTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 56.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 20.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 956\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 9.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" PzNDTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 57.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 32.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1191\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 8.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.605\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" PzNDTDTBO\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 75.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 50\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1175\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 10.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.655\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 10\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 788\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 4.86\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 11.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 806\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 5.03\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 13.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" PIDT-diphQ\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 165.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 68.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1215\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" PIDT-phanQ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 234.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 82.4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1213\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 6.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 6.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PIDT-BTz\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 24.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1465\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 7.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.414\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PIDT-TTz\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 27.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 17.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1271\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.489\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PIDT-TZ\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1211\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 8.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.381\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PIDT-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 21.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1265\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 6.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 6.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 13.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.5670000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" PIDSBT-OCH8\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 18.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1341\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 8.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" PIDSFBT-OCH8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 19.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1377\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 6.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" PIDSBT-C6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 21.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 10.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1164\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 11.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" PIDSFBT-C6\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1200\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 9.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" PIDT-DFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 186.7\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 61.4\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 1105\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 6.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 5.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1\\n\",\n        \"output\": \" 0.5539999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" PIDSe-DFBTL\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 66.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 30.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1200\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 12.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.503\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" PIDSe-DFBTM\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 109.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 46.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1200\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 6.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 12.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.532\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" PIDSe-DFBTH\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 127.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 61.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1200\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 6.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 6.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 13.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1\\n\",\n        \"output\": \" 0.563\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" PDIDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 871\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" PTDIDT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 819\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" PDIDTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 13.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 1035\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" PBSTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 80.4\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 38.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 909\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 8.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 0.488\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" PBSTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 35.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 22.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 1072\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC([Si](CCCCCCCC)(CCCCCCCC)C5=C6C=C7C(C(SC(C)=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)=C5)=C6S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 0.516\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" P-1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 61.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 909\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 9.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC([Si](CCCCCCCC)(CCCCCCCC)C4=C5SC(C6=CC=C(C)C7=NSN=C76)=C4)=C5C=C3[Si]2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" P-2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 80.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1409\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C([Si]2(CCCCCCCC)CCCCCCCC)C=C(C([Si]4(CCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(C6=CC=C(C(N(CCCCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CCCCCCCCCCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" PBDPTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 907\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 10.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5\\n\",\n        \"output\": \" 0.49700000000000005\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" PBDPTFPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 92.1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 26.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 1036\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 9.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5\\n\",\n        \"output\": \" 0.512\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" PBDPTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 19.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1295\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5\\n\",\n        \"output\": \" 0.485\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" PTAT-2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 38.6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 24.1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1417\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" PTAT-3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 47.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 18.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1080\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 15.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" PTAT-4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 45.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 18.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1080\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Monomer as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 9.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" PTB-8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 170.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 83.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 900\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" pDTTG-TPD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 12.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 867\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 5.68\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 13.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PFDTPBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 55.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1079\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 8.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PCDTPBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 121.0\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1094\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 4.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 7.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PCPDTDTPBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 58.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 23.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1091\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 6.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PFDTPQX\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 70.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 34\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1225\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 8.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PCDTPQX\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 50.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 30.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1240\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 8.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" PCPDTDTPQX\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 36.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 17\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1237\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" PThTPTI\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 62.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 28.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 883\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 13.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 0.6559999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" PSeTPTI\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 122.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 34.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 930\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 6.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 6.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" PDTCTTTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 44.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 1436\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 8.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" PDTCTTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 31.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 1307\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 8.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" PDTCTTPQX\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 14.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 1451\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" P4TBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 50.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 1130\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" Si4T-BT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 53.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 970\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 9.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=CC=C(C)C8=NSN=C78)S6\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" Si4T-TPD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 26.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 1100\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 9.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C8C(C(N(CCCCCCCC)C8=O)=O)=C(C)S7)S6\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" Si4T-2FBT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 58.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 40\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 1006\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 14.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si]2(CCCCCCCC)CCCCCCCC)=C(S1)C3=C2C(S4)=C(S3)C5=C4C6=C([Si]5(CCCCCCCC)CCCCCCCC)C=C(C7=C(F)C(F)=C(C)C8=NSN=C87)S6\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" DTBTBT-Bz\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 132.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 1187\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 6.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 6.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" DTBTBT-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 77.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 29\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 1135\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" DTBTBT-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 1191\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" DTAT-Bz\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 46.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 1125\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 4.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" PDITTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 33.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 1295\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 7.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1\\n\",\n        \"output\": \" 0.414\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" PDITTDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 1459\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 10.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1\\n\",\n        \"output\": \" 0.584\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" PFDCTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 16.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 1557\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" PCDCTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 13.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 1572\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PCDCTBT-C8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 61.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 38.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1204\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 4.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 4.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PCDCTDTBT-C8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 30.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 14.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1368\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PCDCTDTDPP-C8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1592\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PCDCTQX-C8\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 14.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1350\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PFDCTBT-C8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 94.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1189\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 12.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.6679999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" PDTPCBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 44.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 36.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 982\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.499\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PDTCCBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 61.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 38.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1204\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" PSiFDCTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 34.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 16.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1470\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" PSiFDCTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 93.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 37.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1341\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCC)C=C9)C%10=CC=C(CCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCC)C=C%12)C%13=CC=C(CCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" PSiFDCTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1729\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C([Si](CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C(N(CC(CC)CCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)=C%10)=C%10C5(C%11=CC=C(CCCCC)C=C%11)C%12=CC=C(CCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCC)C=C%14)C%15=CC=C(CCCCC)C=C%15)S1\\n\",\n        \"output\": \" 0.495\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" PBDCPDT-TPD\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 75.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 24.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1486\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 12.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.622\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" PBDCPDT?FBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 74.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 49.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1393\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 12.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1\\n\",\n        \"output\": \" 0.555\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" PIDTTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 28.2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1357\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 8.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" PIDTTFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 28.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1393\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 10.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" PIDTTTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 62.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 31.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 1486\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 7.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" PIDTT-DFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 61.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1216\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 7.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 7.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 12.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" PTPTPTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 50.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 1875\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 5.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 12.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" PTPTPTQX\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 54.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 2021\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" PIDTCPDT-DFBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 42.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 19.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 2045\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 6.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 6.32\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 14.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" PIDTT-T-DFBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 32.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 17.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 1549\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" PCPDTDFBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 50.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 600\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" PDTPDFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 50.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 672\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 7.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 7.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 17.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" PBDT-BOZ\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 179.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 47.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 676\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 6.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 6.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 0.887\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 0.508\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCzDBSe\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 779\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 7.23\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PF-DTBTA\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 868\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.515\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCz-DTBTA\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 296.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 107.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 883\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" PPh-DTBTA\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 18.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 812\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5\\n\",\n        \"output\": \" 0.561\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PCDTMBI\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 182.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 28.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 741\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" PCPPDTMBI\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 39.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 750\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" PFDTMBI\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 726\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" N-P7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 39.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 862\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Mn of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 9.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1\\n\",\n        \"output\": \" 0.574\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" PECz-DTQx\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 50.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 24.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 1160\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 6.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 6.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 11.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1\\n\",\n        \"output\": \" 0.6579999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" TQ1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 106.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 648\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" PTT-DPP (P1)\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 75.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 14\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 1083\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 15.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" PTT-DPP (P2)\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 78.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 1001\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" PDTSTTz\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 11.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCC)=C(C2=NC(SC(C3=C(CCCCCC)C=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=N7)=C7S2)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 252.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 73.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 932\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.29600000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 817\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.337\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 944\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 7.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.535\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" PCPDTTTz\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 28.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 786\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" PDTSNTDO.\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 16.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 742\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 9.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](C(CC)CCCCC)(C(CCCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" PSiF-DBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 331.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 79\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 732\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C57)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.507\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PDTPBT-C8\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 20.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 579\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 6.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" PDTPBT-C6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 21.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 15.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 523\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 4.86\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" PDTPBT-C5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 29.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 17.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 495\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 4.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 11.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" PDTC\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 693\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 10.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" PDTSi\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 19.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 709\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell HOMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 6.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" PDTP\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 13.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 10.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 708\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 12.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 991\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.536\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 25.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 1027\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 28.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 1120\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6\\n\",\n        \"output\": \" 0.478\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 57.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 1383\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 4.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6\\n\",\n        \"output\": \" 0.688\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" PBBTz-PT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 65.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 1694\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 0.7609999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 5.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" PBBTz-FT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 237.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 107\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 1729\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 6.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 0.8809999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 10.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2\\n\",\n        \"output\": \" 0.649\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" HMPBDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 21.5\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 830\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" PBDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 11.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 964\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" HMPQTN\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 17.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 828\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 5.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1\\n\",\n        \"output\": \" 0.531\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" PQTNBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 962\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 5.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1\\n\",\n        \"output\": \" 0.503\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" PFTTQx\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 22.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 10.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 1099\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" PFTTPz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 31.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 1097\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" PCzTTQx\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 25.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 1114\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" PCzTTPz\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 46.0\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 16.6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 1112\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" PFDCN\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 17.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 845\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 4.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 4.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 9.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" PFPDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 16.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 980\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 4.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 4.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 9.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\\\\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 205.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 59.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 815\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 162.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 48.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 684\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" CPDT-co-TPADCN\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 22.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 9.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 857\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" CPDT-co-TPADTA\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 991\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\\\\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" CPDT-co-TPATCN\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 882\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\\\\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" CPDT-co-FADCN\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 32.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1370\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" CPDT-co-FADTA\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1504\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\\\\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" CPDT-co-FATCN\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 15.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1395\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\\\\C%10=CC=C(/C(C#N)=C(C#N)\\\\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 26.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 18.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 680\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 0.713\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1\\n\",\n        \"output\": \" 0.498\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 45.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 24.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 696\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.5760000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" P3TDTQ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 12.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 8.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1313\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" P3SDTQ\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 15.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1457\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" P3TDTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 8.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 1079\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 10.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" P3SDTDPP\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 17.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1222\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 12.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" P(FBT-alt-Se2Th2)\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 20.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 14.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 1184\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 7.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 7.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 15.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F\\n\",\n        \"output\": \" 0.664\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" H12\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 19.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 14\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 612\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 6.09\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" HEH\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 20.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 500\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" F12\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 648\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" FEH\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 32.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 14\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 536\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 9.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PGeTFDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 103.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1199\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 13.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PGeDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 97.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 39\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1127\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 7.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" PK\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 7.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 760\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.45399999999999996\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" PE\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 8\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 776\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.387\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" pDSBT-BT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 38.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 610\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 6.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 6.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 12.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CCCC)(CCCC)[Si](CCCC)(CCCC)C2=C3SC(C4=CC=C(C)C5=NSN=C54)=C2)=C3S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell average value of PCE. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" PDTSTTz-4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell average value of PCE of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 5.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 5.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 11.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(S1)C2=NC3=C(N=C(C4=CC(CCCCCC)=C(C5=CC([Si](CC(CCCC)CC)(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2\\n\",\n        \"output\": \" 0.716\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" PQS\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 18.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1742\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" PQSQT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 22.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1550\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 9.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" DTS-C6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 29.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 19.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 826\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 4.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 8.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" DTS-T6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 27.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 19.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 832\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 6.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC([Si](CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C(C)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" BDT-C6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 44.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 18.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 854\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" BDT-T6\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 66.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 18.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 860\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C2=C(CCCCCC)SC(CCCCCC)=C2C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" PDTPTBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 22.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 917\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 8.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1\\n\",\n        \"output\": \" 0.42100000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" PDHTT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 12.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 444\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.716\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 8.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" PDOTT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 24.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 500\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 4.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.754\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 7.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" PDDTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 39.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 612\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.7709999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 6.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" PDTBTV\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 36.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 7.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 610\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 4.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 0.335\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" PDTBTFV\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 43.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 646\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 4.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1\\n\",\n        \"output\": \" 0.34600000000000003\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" PTVcBBO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 658\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" PTVtBBO\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 10.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 658\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 0.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 0.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" PEBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 556\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" PEBTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 690\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 4.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell power conversion efficiency of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" PEBTBTTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 854\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" PCzTh-TVCN\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 59.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 830\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.361\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" PCzTh-TVDCN\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 52.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 699\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 5.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\\\\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.365\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" PCzTh-TVDT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 57.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 15.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 833\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 4.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1\\n\",\n        \"output\": \" 0.29100000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" PQTDPP\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 987.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 345\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1217\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 7.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" PQTVTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 691.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 302\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1243\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PBDTNTDO-1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 59.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 24.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 770\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.287\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PBDTNTDO-2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 40.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 742\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.305\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" PBDTNTDO-C1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 6.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 942\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.508\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" PBDTNTDO-C2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 17.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 814\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" PBDTNTDO-C3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 53.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 21.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 798\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 4.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1\\n\",\n        \"output\": \" 0.552\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" PBDTT-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 89.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 40.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 1241\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" PBDTP-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 69.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 36.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1229\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 13.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" PBDTT-FDPP\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 63.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 28.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 1097\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 5.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" PBDTP-FDPP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 41.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 20.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1197\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 7.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PT-Tz-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 41.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1049\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 7.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" PT-Tz-DTffBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 83.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 36.6\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1085\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" PBdT-BTz\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 31.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 972\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1\\n\",\n        \"output\": \" 0.613\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" PBdT-TTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 17.2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 11.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 946\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell weight-averaged molecular weight as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 0.687\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" PBdT-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 19.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 11.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 940\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 4.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1\\n\",\n        \"output\": \" 0.307\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" PBdT-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 14.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 997\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4\\n\",\n        \"output\": \" 0.561\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 60.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 31.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 1320\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 4.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 4.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 11.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1\\n\",\n        \"output\": \" 0.5870000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 60.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 29.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 965\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 5.73\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 9.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1\\n\",\n        \"output\": \" 0.528\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PBDT-TTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 149.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 943\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PBDT-TDPP-S\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 17.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1186\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 10.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PBDT-I\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 168.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1183\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.82\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\\\\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PBDT-TIT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 109.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1347\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.78\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 4.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 7.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" PBDT-OIO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 243.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 90\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1571\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.74\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\\\\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" PBDFTT-C\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 44.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 706\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 10.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1\\n\",\n        \"output\": \" 0.638\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" PBTT-BT (P1)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 254.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 41\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 646\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 6.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" PBTTDPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 19.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 11.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 1020\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 4.96\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell average value of PCE of given SMILES? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" PBTTTTz\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 104.9\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 22.7\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 1395\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 4.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" PBTTTPD\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 35.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 817\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" PBTTTzQx\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 23.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 17.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 1737\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" BTT-BTz\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 42.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 23\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 947\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" PNB-3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 26.5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 14.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 658\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" PNB-4\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 54.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 33.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 1103\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" PBDTTT-EFF\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 886\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 0.693\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 11.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1\\n\",\n        \"output\": \" 0.648\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" PBDTTT-EFT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 44.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 918\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 0.784\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 16.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1\\n\",\n        \"output\": \" 0.682\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" PBDTTT-EFS\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 160.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 69\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 1014\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 8.78\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 8.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 0.807\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 16.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1\\n\",\n        \"output\": \" 0.6559999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" PDBPTBT-2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 99.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 51.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 989\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" PDBPTBT-3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 41.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 21.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 989\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 8.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" PDBPTBT-4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 85.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 62.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 860\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 9.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" PDBPTBT-5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 160.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 33.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 878\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 4.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 7.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 7.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 11.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 30.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 1442\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 4.35\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 4.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 9.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 0.5379999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 128.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 58\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 1478\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 7.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 7.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 15.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10\\n\",\n        \"output\": \" 0.642\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 57.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 38\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 1514\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 7.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 7.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 13.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.556\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" P0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 47.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 21\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 921\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 7.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 7.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.768\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 15.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC\\n\",\n        \"output\": \" 0.636\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" PBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 52.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 24.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1083\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 4.87\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" PFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 95.3\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 41.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1101\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 4.91\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 12.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" PDFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 62.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 29.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1119\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 7.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 14.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" P1-0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 91.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 41.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 504\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 7.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 7.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 13.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" PIDTT-TID\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 131.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 35.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 1362\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 5.89\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" PBDD-ff4T\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 80.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 56.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 1060\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 8.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 13.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDPP-OD\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 410.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 114\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1465\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" PBDB-TT0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 49.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 15.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 1212\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 7.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 7.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 0.8859999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 11.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1\\n\",\n        \"output\": \" 0.6990000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" PTB7-TV\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 53.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 866\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 8.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 8.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 15.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" PBDT-NQx\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 53.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 38\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 1889\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 11.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 0.601\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" PBDTS-NQx\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 68.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 40\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 1953\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 7.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 6.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 12.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" PDPPTT-2T\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 205.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 106.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1027\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 15.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" PDPPMT-2T\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 229.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 138.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 873\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 6.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 15.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" PffBX4T-2OD\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 189.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 102\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 1185\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 9.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 9.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 0.875\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 15.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" PTBI2T\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 183.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 76.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1309\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" PTBI2TR\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 984.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 65.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1421\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 15.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" PTBITT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 114.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 56.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1283\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 5.85\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" PTBI2Tz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 517.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 114\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1311\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 6.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 4.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" PBDTDTBT-H\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 165.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 98.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 1057\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 5.03\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 7.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 7.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 13.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 0.665\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" PBDTDTBT-R\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 282.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 120.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 1185\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 5.01\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 8.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 8.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 13.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 0.7170000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" PBDTDTffBT-H\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 127.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 63.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 1092\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 9.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 9.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 14.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8\\n\",\n        \"output\": \" 0.7190000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" PBDTDTffBT-R\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 153.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 71.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 1221\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 5.03\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 9.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 9.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 13.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8\\n\",\n        \"output\": \" 0.7390000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" PBDTTT-H\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 181.5\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 73.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 846\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 9.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 9.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 17.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6\\n\",\n        \"output\": \" 0.675\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" PBDTTT-R\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 101.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 46.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 974\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Monomer of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 5.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 12.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6\\n\",\n        \"output\": \" 0.5760000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 70.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 48.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 652\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 16.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 86.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 56.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 670\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 5.13\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 6.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 6.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 18.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 89.8\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 53.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 688\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 9.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 9.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 20.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 188.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 23.3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 1637\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 5.05\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 8.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 4.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 4.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 10.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 0.593\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 87.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 22.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 1655\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 5.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 12.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 0.602\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 106.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 25.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 1673\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 4.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 8.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 8.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 14.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" PzIIG-BDT2TC8\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 69.4\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 28.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 1419\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 7.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 0.6559999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" PzIIG-BTT2TC10\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 51.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 23.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 1643\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 5.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\\\\4=O)C=N3)=O)=C2C=C1\\n\",\n        \"output\": \" 0.608\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" PMOT5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 112.5\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 45.9\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 1272\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 9.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 9.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 13.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell PCE of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" PBDTBDD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 75.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 1212\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 3.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 6.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 6.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 12.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" PMOT2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 52.7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1403\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 8.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 7.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 13.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell open-circuit voltage of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" PBQ-3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 47.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 23.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1343\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 6.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 11.73\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" PBDTBO-CIBTDD\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 113.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 36.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1218\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 9.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 9.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 16.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.7170000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" PBDTBO-CIBTEH\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 88.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 32.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1162\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 6.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 6.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 13.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.631\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" PBDTHD-CIBTEH\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 58.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 21.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1275\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 10.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.644\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" PBDTHD-CIBTDD\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 38.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 17.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1331\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 4.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 11.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9\\n\",\n        \"output\": \" 0.623\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" PBPD-Th\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 107.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 1233\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 8.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 12.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" PBPD-Se\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 92.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 48\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 1328\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 9.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 14.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" PBDTT-O-TT-CF\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 34.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 920\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 8.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 8.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 16.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" PBDTT-S-TT-CF\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 51.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 952\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 9.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 9.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 15.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" PIDTBDTID\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 36.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 21.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 2229\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 7.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\\\\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" PIDTBDT(ID)2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 13.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 3144\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 6.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\\\\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\\\\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1\\n\",\n        \"output\": \" 0.423\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 49.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 1100\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 35.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1372\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 7.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.609\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 20.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1452\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.18\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 6.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.588\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" PBDT-TSR\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 63.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 30\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 1934\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 9.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 0.804\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 17.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1\\n\",\n        \"output\": \" 0.706\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" PDPP[T]2-EDOT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 383.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 142\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 917\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.73\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 15.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" PDPP[Py]2-EDOT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 61.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 25.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 907\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 6.07\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" PDPP[Ph]2-EDOT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 35.1\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 16.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 905\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 5.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" PBDTA-INDI\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 249.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 61.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 1463\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 5.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 4.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 8.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1\\n\",\n        \"output\": \" 0.637\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" PBDTT-INDI\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 165.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 48.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 1595\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 6.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 6.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 10.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1\\n\",\n        \"output\": \" 0.645\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 39.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 16.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 1141\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 154.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 42.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 1177\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 5.72\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 9.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 9.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 14.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" PIDT-DTQ-T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 46.2\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2253\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 11.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.6579999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" PIDT-DTQ-TT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 46.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2309\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 6.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 6.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 12.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" PBTF-OP\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 134.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 64.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 938\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 9.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 16.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1\\n\",\n        \"output\": \" 0.622\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" PCDPP\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 705.8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 136\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1948\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 9.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 9.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 16.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell power conversion efficiency. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" PF0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 53.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 28\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1465\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 11.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.655\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" PF1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 35.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1483\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 6.29\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 6.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 11.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.662\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" PF2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 39.8\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 24\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1501\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 6.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 6.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 11.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" PIDTT-TT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 60.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 32.5\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1184\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 3.11\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 7.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 6.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 10.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" PIDTV-ffBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 90.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 908\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 17.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" PDFBC-DPP\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 124.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 73.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 1379\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 3.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 13.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" P-2T\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 108.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 45.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 1365\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 7.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 7.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 17.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F\\n\",\n        \"output\": \" 0.595\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" P-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 125.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 1339\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell number-averaged molecular weight as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 9.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 9.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 18.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F\\n\",\n        \"output\": \" 0.6859999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" PBDTT-DTFPQx\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 81.0\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 43.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 1343\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 5.52\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 11.4\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" PC1BT6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 134.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1220\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 7.34\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 7.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 0.552\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" PC2BT6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 34.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 20.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1234\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 6.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 6.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 13.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" PC6BT6\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 47.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 27.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1290\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 6.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 12.91\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 0.505\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" PNC2C4BT6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 52.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 25.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 1122\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 6.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 6.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 13.24\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1\\n\",\n        \"output\": \" 0.509\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" PC2BT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 19.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 11.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1202\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 10.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" PBDTT-BTAZT-1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 67.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 32.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 1211\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 6.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 6.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 14.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 0.624\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" PBDTT-BTAZT-2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 70.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 30.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 1195\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 5.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 6.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 5.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 12.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1\\n\",\n        \"output\": \" 0.624\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" PIDTI-BT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 46.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 26.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 2095\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 8.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1\\n\",\n        \"output\": \" 0.546\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" PIDTI-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 122.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 76.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 2259\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 5.26\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 9.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1\\n\",\n        \"output\": \" 0.514\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" h-PPDTNTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 15.7\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 9.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 993\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 4.44\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 13.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" d-PPDTNTz\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 115.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 46\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 1217\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 6.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 6.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 14.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" PDVF-8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 178.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 63.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 1047\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 8.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 0.6409999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" PDVF-10\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 86.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 26.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 1159\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 4.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 10.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1\\n\",\n        \"output\": \" 0.6659999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" PtBTPBDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 133.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 70\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 1149\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 4.03\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 9.09\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" PtFBTPBDT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 106.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 53\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 1185\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 3.11\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 5.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell VOC of given SMILES? ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" PtBTPDPP\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 131.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 61.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 1227\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\\\\4C=CC=C%10)=C3S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" PtFBTPDTS\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 78.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 20\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 822\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 5.09\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 6.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC([Si](CCCCCCCC)(CCCCCCCC)C7=C8SC(C)=C7)C8S6)S4)/C9=C5C=C(F)C=C9\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" PtBTPIDT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 48.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 35.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 1273\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 10.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\\\\4C=CC=C%15)=C3S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell VOC of given SMILES. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" PcBTPBDT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 70.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 1149\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 39.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 917\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 6.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 11.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" PTSSO-TT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 27.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 15.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 850\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 11.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" PTSSO-BDT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 63.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 26\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 1157\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 7.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" PQx\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 66.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 25.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 1675\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 8.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" PphQx\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 66.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 23.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 1673\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 5.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 4.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 10.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" PBDT(ff)-ttTPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 105.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 1554\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 7.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 7.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 12.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" PBDTT-ttTPD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 90.3\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 1482\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 5.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 6.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 6.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 12.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTOT-FBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 29.8\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 17.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1228\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 8.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.603\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTOT-BT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 24.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 13.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1192\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.369\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDTOT-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 29.2\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1249\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 8.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.47200000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" PBDTBTz-T\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 44.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 22.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1413\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 6.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 6.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 10.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.629\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" PBT-2TPF4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 12.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 10.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 1201\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 5.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 5.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 0.8540000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 10.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 0.606\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" PffBT-2TPF4\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 1237\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 5.84\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 4.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 1.0170000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 6.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1\\n\",\n        \"output\": \" 0.526\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" PBDD4T\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 29.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 12.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 1024\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 6.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 11.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" PBDD4T-2F\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 44.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 22.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 1060\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 9.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 8.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 15.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" P(BT-DPP)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 42.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1165\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" P(BT-DPP)-T\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 24.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 13.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1165\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 6.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" PBDTfDTBO-L\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 21.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 15.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1337\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.455\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" PBDTfDTBT-L\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 32.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 14.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1353\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 4.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 8.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" PBDTfDTBS-L\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 27.6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 15.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1400\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 9.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.674\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 85.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 34\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1140\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 4.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 8.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 142.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1196\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 4.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 10.31\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 149.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1253\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 7.13\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 7.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 12.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" PFBDT-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 71.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 45.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 1293\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 7.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 7.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 13.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 0.598\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" PFBDT-DTffBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 62.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 57.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 1329\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 5.82\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 7.15\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 13.24\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1\\n\",\n        \"output\": \" 0.5770000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" P2-Ome\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 114.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 67.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 1391\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 7.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1\\n\",\n        \"output\": \" 0.506\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" PTZ6\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 58.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 31.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 1353\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 8.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 7.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1\\n\",\n        \"output\": \" 0.767\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 26.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 12.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 940\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 20.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 924\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 12.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 8.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 879\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 10.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 947\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" PThzTITI\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 130.6\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 62.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 1045\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 0.568\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" PSezTITI\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 305.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 85.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 1093\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7\\n\",\n        \"output\": \" 0.596\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" PVB1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 60.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 23.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 996\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" PVB2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 51.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 28.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 869\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" P(BDTT-BTBDPPD)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 84.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 26\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 1987\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 4.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 4.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 7.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" PDTfBO-T\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 53.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 31.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 1067\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 5.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1\\n\",\n        \"output\": \" 0.5429999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" PDTfBO-DT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 75.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 37.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 1149\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" PDTfBO-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 50.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 31.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 1123\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 9.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1\\n\",\n        \"output\": \" 0.664\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" poly(DPP-alt-BP)\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 380.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 194\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1153\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 7.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.36200000000000004\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" poly(DPP-alt-BT)\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 304.4\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 139\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1165\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 9.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" poly(DPP4T-alt-TBP)\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 304.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 150\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2288\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 4.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 4.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 10.08\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.633\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" PBDT-DTQ\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 30.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 1925\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 10.37\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2\\n\",\n        \"output\": \" 0.555\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" PIDT-DTQ\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 46.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 2253\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 6.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 11.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11\\n\",\n        \"output\": \" 0.6579999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" P8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 74.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 42.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 894\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 6.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 6.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 14.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 0.621\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" P9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 43.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 29.2\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 942\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 6.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 6.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 14.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1\\n\",\n        \"output\": \" 0.6459999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" r-PTTDPP50\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 203.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 170.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 1149\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 0.632\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 9.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1\\n\",\n        \"output\": \" 0.374\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" DT-PDPP2T-TT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 2535.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 780\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1139\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 11.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" PIIDBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 139.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 45.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 1015\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 4.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 4.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 8.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 0.619\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" PIIDFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 198.1\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 75.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 1051\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 5.79\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 6.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 9.11\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O\\n\",\n        \"output\": \" 0.672\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" PHBCDPPC20\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 24.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1881\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 0.353\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" PHBCDPPC8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 69.0\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1545\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 10.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 0.318\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" PHBCDPPF\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 41.0\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 11\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1849\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 6.39\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1\\n\",\n        \"output\": \" 0.336\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" PHBCDPPDT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 34.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 2045\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 5.19\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1\\n\",\n        \"output\": \" 0.331\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 39.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 13.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 917\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 5.44\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 6.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 6.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 11.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" P(BDTT-TTBDPPD)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 169.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 1961\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 8.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PA\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 124.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 48.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1072\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.855\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 8.669\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.506\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" PB\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 25.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 14.1\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 1100\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 5.66\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell HOMO of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 0.769\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 6.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9\\n\",\n        \"output\": \" 0.456\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" PC\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 18.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 8.2\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 852\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 5.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 0.861\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 6.914\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" PHF\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 137.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 52.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 1671\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 7.2\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 6.95\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 12.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" PFH\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 87.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 54.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 1671\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 6.19\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 5.96\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 9.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" PFF\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 139.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 63.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 1707\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 4.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" P\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 23.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 9.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1587\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 7.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 7.42\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 16.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1969\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 7.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 7.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 12.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 13.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 8.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1829\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 6.68\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 6.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 11.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(CCCCCCCCCCCC)C=C(S1)C2=C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S3)=C3C4=C5N=C(C(CC)CCCCCCCCCCCCCCCC)S4)C5=N6)C6=C(C7=NSN=C72)C8=CC(CCCCCCCCCCCC)=C(S8)C9=CC%10=C(C(SC(C)=C%11)=C%11[Si]%10(CCCCCCCC)CCCCCCCC)S9\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" PBDT-TPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 38.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 25.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 869\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1\\n\",\n        \"output\": \" 0.392\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" PBDT-Th-TPD\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 153.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 73\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1033\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 4.17\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.361\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" PBDT-TT-TPD\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 16.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 1145\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 4.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 0.37200000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" PDPP2TPCL\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 240.2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 72.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 1323\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 5.06\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 4.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" PTTABT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 106.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 54\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 1228\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 4.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 4.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 10.19\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1\\n\",\n        \"output\": \" 0.6579999999999999\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" PTTABDT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 113.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 61.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 1247\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 5.33\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 5.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 10.52\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1\\n\",\n        \"output\": \" 0.654\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" P4,9-BNDTDTFBT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 47.1\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 24.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 1163\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 7.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 7.23\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 11.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" P5,10-BNDTDTFBT\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 25.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 16.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 1163\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 12.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1\\n\",\n        \"output\": \" 0.605\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" P(BDP-DTPz)\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 32.5\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1173\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 6.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.8590000000000001\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 204.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 68.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 978\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 6.87\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 6.71\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 12.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 200.3\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 74.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1007\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 8.27\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 8.04\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 14.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 217.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 77.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1063\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.7\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 13.89\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 197.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 70.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1119\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.57\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 12.81\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" P5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 275.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 86\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1175\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.61\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 6.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 6.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 10.61\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" PBDT-DFQX-TTSEH\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 169.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 45.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 1386\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 5.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell band gap of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 7.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 6.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 12.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1\\n\",\n        \"output\": \" 0.6609999999999999\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" PBDT-DFQX-TTSC8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 116.9\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 40.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 1386\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 5.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 8.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 8.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 14.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1\\n\",\n        \"output\": \" 0.682\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 19.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 12.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1122\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 5.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 20.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 11.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1254\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 5.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell band gap as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 6.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell open-circuit voltage of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" PDPP-SS\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 110.8\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 71\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1261\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.25\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 6.46\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" PDPP-TT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 304.4\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 139\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1165\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 7.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" PBDPBT-T\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 28.1\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 23.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 1028\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1\\n\",\n        \"output\": \" 0.5770000000000001\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" PBDPBT-TT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 27.9\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 9.6\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 1140\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 3.32\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1\\n\",\n        \"output\": \" 0.47600000000000003\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" PBDPBT-biT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 34.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 21.3\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 1192\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 5.35\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 8.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1\\n\",\n        \"output\": \" 0.594\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" BTzDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 47.5\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1066\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 10.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" BTzDTFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 59.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 23\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1084\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 12.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" BTzDT2FBT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 94.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1102\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 7.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 14.64\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" PDPPHT-TBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 35.5\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 20.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 1217\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Mn as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 11.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" PDPPHT-BDTT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 25.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 14.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 1297\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 7.26\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" PBBDTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 130.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 43\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 1437\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 5.43\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 3\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 4.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 8.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" PBDTT-fDTBO\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 123.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 88.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1173\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.64\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 5.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1\\n\",\n        \"output\": \" 0.496\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" PBDTO-fDTBO\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 172.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 89.3\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1041\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1\\n\",\n        \"output\": \" 0.507\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" TBFPF-BT\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 53.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 38.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 1201\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 5.28\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 12.12\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" TBFPF-BO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 51.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 32.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 1185\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 5.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 5.98\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell average value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 10.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 21.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 12.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1648\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 12.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.583\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 30.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1519\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.14\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell poly dispersity index as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 9.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.645\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" P3\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 35.0\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 24.3\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1555\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.451\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" P4\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 62.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 40.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1484\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 5.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O\\n\",\n        \"output\": \" 0.653\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" PSB-DFBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 58.3\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 30.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 1053\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell average value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 6.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" PSB-DTDFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 83.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 40.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 1385\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write poly dispersity index of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell average value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell Jsc of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" PSB-FTT\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 247.8\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 99.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 1195\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 5.21\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 4.45\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 4.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 9.5\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" LGC-D013\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 61.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 49.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 1715\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 5.56\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell poly dispersity index of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 7.22\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 6.99\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 11.29\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1\\n\",\n        \"output\": \" 0.731\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" TQF2-1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 64.4\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 26.9\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 684\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 6.18\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" PTI-1\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 127.0\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 44\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 821\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 5.78\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\\\\3)=O)C=C1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" PR11\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 90.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 34.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 1475\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 5.88\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\\\\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" PIDTT-DTBO\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 73.7\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 33.5\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1505\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 5.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 4.47\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.49700000000000005\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell short-circuit current density. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" PIDTT-DTBT\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 72.7\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 30.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1521\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 5.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 4.91\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 4.79\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 10.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" PTBTfBTzSi\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 20.2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 1182\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 4.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell PDI of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 9.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(F)C=C(C5=CC6=C(C(SC(C7=CC(F)=C(C)C8=NN(CCCCCC)N=C78)=C9)=C9[Si]6(CCCCCCCC)CCCCCCCC)S5)C%10=NN(CCCCCC)N=C4%10)S3)C%11=NSN=C2%11)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" PBDTS-FBT\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 9.3\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 8.9\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 840\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 6.65\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.303\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" PBDTS-DTFBT\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 34.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 25.2\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1172\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell LUMO of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 8.27\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell short-circuit current density of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 0.46399999999999997\\n\"\n    },\n    {\n        \"instruction\": \"What is nickname of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" PBDT-TPD\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mn at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 933\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write PDI of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell Jsc as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 5.23\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell FF of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1\\n\",\n        \"output\": \" 0.41600000000000004\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" PBDTS-DPP\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 10.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 6.7\\n\"\n    },\n    {\n        \"instruction\": \"What is Mw of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1192\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write LUMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell LUMO as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 7.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1\\n\",\n        \"output\": \" 0.396\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" PDTTDPP-EH\\n\"\n    },\n    {\n        \"instruction\": \"Write Mw of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 46.8\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 13\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 1247\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 5.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its band gap at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" PDTTDPP-BO\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 64.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Mn of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 1359\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 5.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its poly dispersity index at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell VOC as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 10.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell FF of given SMILES? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" PTTIBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 24.0\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 18\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 655\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 5.32\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its nickname. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" PTTIMBI\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 27.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 12\\n\"\n    },\n    {\n        \"instruction\": \"What is Monomer of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 665\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its HOMO at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 5.29\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its PDI at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell open-circuit voltage as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" pDSBT-BHTBT\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 14.7\\n\"\n    },\n    {\n        \"instruction\": \"What is number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 9.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its number-averaged molecular weight at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 942\\n\"\n    },\n    {\n        \"instruction\": \"Write number-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its LUMO at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is PDI of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell PDI as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell VOC of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell short-circuit current density as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 8.64\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell fill factor of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7[Si](CCCC)(CCCC)[Si]2(CCCC)CCCC)S1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" P1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Mw at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 25.1\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 13.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its Monomer at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1264\\n\"\n    },\n    {\n        \"instruction\": \"What is HOMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.49\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is poly dispersity index of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of PCE as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell open-circuit voltage of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell Jsc of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell FF as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Write nickname of given SMILES. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" P2\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 21.4\\n\"\n    },\n    {\n        \"instruction\": \"What is Mn of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 12.6\\n\"\n    },\n    {\n        \"instruction\": \"Write Monomer of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1264\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 5.41\\n\"\n    },\n    {\n        \"instruction\": \"Write HOMO of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 7.48\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell solar cell solar cell solar cell solar cell maximum value of power conversion efficiency. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" BDT8TT\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 49.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its weight-averaged molecular weight at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 26\\n\"\n    },\n    {\n        \"instruction\": \"What is weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 988\\n\"\n    },\n    {\n        \"instruction\": \"Write weight-averaged molecular weight of given SMILES at room temperature and atmospheric pressure. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"What is LUMO of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given SMILES at normal measurement conditions.. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given SMILES at normal measurement conditions.? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell maximum value of power conversion efficiency as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM? ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write solar cell solar cell solar cell PCE of given SMILES as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its solar cell fill factor as a p-type polymer and PC71BM or PCBM. ->\",\n        \"input\": \" CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1\\n\",\n        \"output\": \" 0.473\\n\"\n    }\n]"
  },
  {
    "path": "dataset/NagasawaOPV/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 6,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"15639\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('NagasawaOPV.csv')\\n\",\n    \"slot = {\\\"Nickname\\\":[\\\"nickname\\\"], \\n\",\n    \"        \\\"SMILES\\\":[\\\"SMILES\\\"], \\n\",\n    \"        \\\"PCE_max(%)\\\":[\\\"maximum value of PCE\\\", \\\"maximum value of power conversion efficiency\\\"], \\n\",\n    \"        \\\"PCE_ave(%)\\\":[\\\"average value of PCE\\\", \\\"average value of power conversion efficiency\\\", \\\"PCE\\\", \\\"power conversion efficiency\\\"],\\n\",\n    \"        \\\"Voc (V)\\\":[\\\"VOC\\\", \\\"open-circuit voltage\\\"], \\n\",\n    \"        \\\"Jsc (mA cm^2)\\\":[\\\"Jsc\\\", \\\"short-circuit current density\\\"], \\n\",\n    \"        \\\"FF\\\":[\\\"FF\\\", \\\"fill factor\\\"], \\n\",\n    \"        \\\"Mw (kg mol^-1)\\\":[\\\"Mw\\\", \\\"weight-averaged molecular weight\\\"], \\n\",\n    \"        \\\"Mn (kg mol^-1)\\\":[\\\"Mn\\\", \\\"number-averaged molecular weight\\\"],\\n\",\n    \"        \\\"PDI (=Mw/Mn)\\\":[\\\"PDI\\\", \\\"poly dispersity index\\\"], \\n\",\n    \"        \\\"Monomer (g mol^-1)\\\":[\\\"Monomer\\\"], \\n\",\n    \"        \\\"HOMO (eV)\\\":[\\\"HOMO\\\"], \\n\",\n    \"        \\\"LUMO (eV)\\\":[\\\"LUMO\\\"], \\n\",\n    \"        \\\"bandgap(eV)\\\":[\\\"band gap\\\"]}\\n\",\n    \"pair1 = [(\\\"Nickname\\\", \\\"SMILES\\\"),\\n\",\n    \"        (\\\"Mw (kg mol^-1)\\\", \\\"SMILES\\\"),\\n\",\n    \"        (\\\"Mn (kg mol^-1)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"Monomer (g mol^-1)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"HOMO (eV)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"LUMO (eV)\\\", \\\"SMILES\\\"),\\n\",\n    \"        (\\\"bandgap(eV)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"PDI (=Mw/Mn)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"PCE_max(%)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"PCE_ave(%)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"Voc (V)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"Jsc (mA cm^2)\\\", \\\"SMILES\\\"), \\n\",\n    \"        (\\\"FF\\\", \\\"SMILES\\\")]\\n\",\n    \"pc_tem = [\\\"PCE_max(%)\\\", \\\"PCE_ave(%)\\\", \\\"Voc (V)\\\", \\\"Jsc (mA cm^2)\\\", \\\"FF\\\"]\\n\",\n    \"'''\\n\",\n    \"pair2 = [(\\\"SMILES\\\", \\\"Nickname\\\"),\\n\",\n    \"         (\\\"SELFIES\\\", \\\"compound\\\"),\\n\",\n    \"         (\\\"InChI\\\", \\\"compound\\\")]\\n\",\n    \"'''\\n\",\n    \"data_list = []\\n\",\n    \"for df_slice in df.iterrows():\\n\",\n    \"    for p in pair1:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran1 = random.randint(0,2)\\n\",\n    \"        ran2 = random.randint(0, len(slot[p[0]]))\\n\",\n    \"        for i in range(0,len(slot[p[0]])):\\n\",\n    \"            if i == ran2:\\n\",\n    \"                pn = slot[p[0]][i]\\n\",\n    \"        if p[0] == \\\"Nickname\\\":\\n\",\n    \"            if ran1 == 0:\\n\",\n    \"                question = \\\"What is \\\"+ pn + \\\" of given \\\" + p[1] + \\\"? ->\\\"\\n\",\n    \"            elif ran1 == 1:\\n\",\n    \"                question = \\\"Write \\\" + pn + \\\" of given \\\" + p[1] + \\\". ->\\\"\\n\",\n    \"            elif ran1 == 2:\\n\",\n    \"                question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ pn + \\\". ->\\\"\\n\",\n    \"        else:\\n\",\n    \"            if p[0] in pc_tem:\\n\",\n    \"                tem = \\\" as a p-type polymer and PC71BM or PCBM\\\"\\n\",\n    \"                pn = \\\"solar cell \\\"+pn\\n\",\n    \"            else:\\n\",\n    \"                ran3 = random.randint(0,1)\\n\",\n    \"                if ran3 == 0:\\n\",\n    \"                    tem = \\\" at room temperature and atmospheric pressure\\\"\\n\",\n    \"                else:\\n\",\n    \"                    tem = \\\" at normal measurement conditions.\\\"\\n\",\n    \"            if ran1 == 0:\\n\",\n    \"                question = \\\"What is \\\"+ pn + \\\" of given \\\" + p[1] + tem + \\\"? ->\\\"\\n\",\n    \"            elif ran1 == 1:\\n\",\n    \"                question = \\\"Write \\\" + pn + \\\" of given \\\" + p[1] + tem + \\\". ->\\\"\\n\",\n    \"            elif ran1 == 2:\\n\",\n    \"                question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ pn + tem + \\\". ->\\\"\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] = \\\" \\\"+str(df_slice[1][p[1]])+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(df_slice[1][p[0]])+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\\n\",\n    \"print(len(data_list))\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 7,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"15639\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"print(len(data_list))\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('NagasawaOPV.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"ce1a9f8a\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.6.13\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/Pei/Pei.csv",
    "content": "Alloy,Phase\nAg0.05Zr0.95,bcc\nAl0.15Cr0.85,bcc\nAl0.1Fe0.9,bcc\nAl0.1Hf0.9,bcc\nAl0.1Ti0.9,bcc\nAl0.1W0.9,bcc\nAl0.2Fe0.8,bcc\nAl0.2Ti0.8,bcc\nAl0.2V0.8,bcc\nAl0.3Cr0.7,bcc\nAl0.3Nb1Ta0.8Ti1.4V0.2Zr1.3,bcc\nAl0.4Hf0.6Nb1Ta1Ti1Zr1,bcc\nAl0.4V0.6,bcc\nAl0.75Hf1Nb1Ta1Ti1Zr1,bcc\nAl1Cr0.5Nb1Ti1V1,bcc\nAl1Cr1Mo1Ti1W1,bcc\nAl1Nb1.5Ta0.5Ti1.5Zr0.5,bcc\nAl1Nb1Ta1Ti1V1,bcc\nAl1Nb1Ti1V1,bcc\nAu0.05Ta0.95,bcc\nAu0.05Ti0.95,bcc\nAu0.08V0.92,bcc\nAu0.1Nb0.9,bcc\nAu0.1Zr0.9,bcc\nBa0.25Ca0.75,bcc\nBa0.25Eu0.75,bcc\nBa0.25Eu0.75,bcc\nBa0.25Sr0.75,bcc\nBa0.25Yb0.75,bcc\nBa0.5Ca0.5,bcc\nBa0.5Eu0.5,bcc\nBa0.5Eu0.5,bcc\nBa0.5Sr0.5,bcc\nBa0.5Yb0.5,bcc\nBa0.75Ca0.25,bcc\nBa0.75Eu0.25,bcc\nBa0.75Eu0.25,bcc\nBa0.75Sr0.25,bcc\nBa0.75Yb0.25,bcc\nBe0.02W0.98,bcc\nCa0.25Sr0.75,bcc\nCa0.5Sr0.5,bcc\nCa0.75Sr0.25,bcc\nCa0.7Yb0.3,bcc\nCa0.85Yb0.15,bcc\nCo0.1Cr0.9,bcc\nCr0.05Ta0.95,bcc\nCr0.1Nb0.9,bcc\nCr0.25Fe0.75,bcc\nCr0.25Mo0.75,bcc\nCr0.25V0.75,bcc\nCr0.2W0.8,bcc\nCr0.5Fe0.5,bcc\nCr0.5Mn0.5,bcc\nCr0.5Mo0.5,bcc\nCr0.5V0.5,bcc\nCr0.75Fe0.25,bcc\nCr0.75Mn0.25,bcc\nCr0.75Mo0.25,bcc\nCr0.75V0.25,bcc\nCr0.85Ru0.15,bcc\nCr0.8Re0.2,bcc\nCr0.95Ir0.05,bcc\nCr0.9Os0.1,bcc\nCr0.9W0.1,bcc\nCr1Mo1Nb1Re1Ta1V1W1,bcc\nCr1Mo1Nb1Ta1V1W1,bcc\nCs0.25Rb0.75,bcc\nCs0.5Rb0.5,bcc\nCs0.75Rb0.25,bcc\nFe0.1V0.9,bcc\nFe0.85Zn0.15,bcc\nFe0.8V0.2,bcc\nFe0.93Si0.07,bcc\nFe0.9Ga0.1,bcc\nFe0.9Rh0.1,bcc\nGa0.15Ti0.85,bcc\nHf0.25Nb0.75,bcc\nHf0.25Ta0.75,bcc\nHf0.25Ti0.75,bcc\nHf0.25Zr0.75,bcc\nHf0.5Nb0.5,bcc\nHf0.5Ta0.5,bcc\nHf0.5Ti0.5,bcc\nHf0.5Zr0.5,bcc\nHf0.75Nb0.25,bcc\nHf0.75Ta0.25,bcc\nHf0.75Ti0.25,bcc\nHf0.75Zr0.25,bcc\nHf1Mo1Nb1Ti1Zr1,bcc\nHf1Nb1Ta1Ti1V1Zr1,bcc\nHf1Nb1Ta1Ti1Zr1,bcc\nHf1Nb1Ta1Zr1,bcc\nHf1Nb1Ti1V1Zr1,bcc\nHf1Nb1Ti1Zr1,bcc\nIr0.02W0.98,bcc\nIr0.05Mo0.95,bcc\nIr0.05Nb0.95,bcc\nIr0.05Ta0.95,bcc\nIr0.05Ti0.95,bcc\nIr0.1V0.9,bcc\nLi0.35Mg0.65,bcc\nLi0.5Mg0.5,bcc\nLi0.85Mg0.15,bcc\nMn0.25V0.75,bcc\nMn0.5V0.5,bcc\nMn0.6V0.4,bcc\nMn0.7V0.3,bcc\nMo0.25Nb0.75,bcc\nMo0.25Ta0.75,bcc\nMo0.25Ti0.75,bcc\nMo0.25V0.75,bcc\nMo0.25W0.75,bcc\nMo0.5Nb0.5,bcc\nMo0.5Ta0.5,bcc\nMo0.5Ti0.5,bcc\nMo0.5V0.5,bcc\nMo0.5W0.5,bcc\nMo0.75Nb0.25,bcc\nMo0.75Re0.25,bcc\nMo0.75Ta0.25,bcc\nMo0.75Ti0.25,bcc\nMo0.75V0.25,bcc\nMo0.75W0.25,bcc\nMo0.7Tc0.3,bcc\nMo0.8Tc0.2,bcc\nMo0.95Os0.05,bcc\nMo0.95Rh0.05,bcc\nMo0.98Pd0.02,bcc\nMo0.9Re0.1,bcc\nMo0.9Ru0.1,bcc\nMo0.9Tc0.1,bcc\nMo1Nb1Re1Ta1Ti1V1W1,bcc\nMo1Nb1Re1Ta1V1W1,bcc\nMo1Nb1Re1Ta1W1,bcc\nMo1Nb1Ta1Ti1V1,bcc\nMo1Nb1Ta1Ti1V1W1,bcc\nMo1Nb1Ta1V1,bcc\nMo1Nb1Ta1V1W1,bcc\nMo1Nb1Ta1W1,bcc\nMo1Nb1Ti1V1Zr1,bcc\nMo21.7Nb20.6Ta15.6V21W21.1,bcc\nMo25.6Nb22.7Ta24.4W27.3,bcc\nNb0.25Ta0.75,bcc\nNb0.25Ti0.75,bcc\nNb0.25W0.75,bcc\nNb0.25Zr0.75,bcc\nNb0.5Ta0.5,bcc\nNb0.5Ti0.5,bcc\nNb0.5W0.5,bcc\nNb0.5Zr0.5,bcc\nNb0.65Ru0.35,bcc\nNb0.6Re0.4,bcc\nNb0.75Re0.25,bcc\nNb0.75Ta0.25,bcc\nNb0.75Ti0.25,bcc\nNb0.75W0.25,bcc\nNb0.75Zr0.25,bcc\nNb0.8Pd0.2,bcc\nNb0.9Os0.1,bcc\nNb0.9Pd0.1,bcc\nNb0.9Re0.1,bcc\nNb0.9Rh0.1,bcc\nNb0.9Ru0.1,bcc\nNb1Re1Ta1Ti1V1,bcc\nNb1Ta1Ti1V1,bcc\nNb1Ta1Ti1V1W1,bcc\nNb1Ta1V1W1,bcc\nNb1Ti1V1Zr1,bcc\nNd0.25Th0.75,bcc\nNd0.5Th0.5,bcc\nNd0.75Th0.25,bcc\nOs0.05W0.95,bcc\nOs0.15Ta0.85,bcc\nOs0.15Ti0.85,bcc\nPd0.1V0.9,bcc\nPd0.2V0.8,bcc\nPr0.25Th0.75,bcc\nPr0.5Th0.5,bcc\nPr0.75Th0.25,bcc\nPt0.05V0.95,bcc\nPu0.25Sc0.75,bcc\nPu0.25Zr0.75,bcc\nPu0.5Sc0.5,bcc\nPu0.5Zr0.5,bcc\nPu0.75Sc0.25,bcc\nPu0.75Zr0.25,bcc\nRe0.1Ta0.9,bcc\nRe0.1Ti0.9,bcc\nRe0.1V0.9,bcc\nRe0.1W0.9,bcc\nRe0.25Ti0.75,bcc\nRe0.25V0.75,bcc\nRe0.25W0.75,bcc\nRe0.2Ta0.8,bcc\nRe0.4Ta0.6,bcc\nRe0.4Ti0.6,bcc\nRe0.5V0.5,bcc\nRh0.15Ti0.85,bcc\nRh0.1Ta0.9,bcc\nRh0.1V0.9,bcc\nRu0.1Ta0.9,bcc\nRu0.1Ti0.9,bcc\nRu0.1W0.9,bcc\nRu0.2Ta0.8,bcc\nRu0.2Ti0.8,bcc\nRu0.2W0.8,bcc\nSc0.25Th0.75,bcc\nSc0.25Ti0.75,bcc\nSc0.25Y0.75,bcc\nSc0.2Zr0.8,bcc\nSc0.4Zr0.6,bcc\nSc0.5Th0.5,bcc\nSc0.5Ti0.5,bcc\nSc0.5Y0.5,bcc\nSc0.75Th0.25,bcc\nSc0.75Ti0.25,bcc\nSc0.75Y0.25,bcc\nSm0.25Y0.75,bcc\nSm0.5Y0.5,bcc\nSm0.75Y0.25,bcc\nTa0.25Ti0.75,bcc\nTa0.25V0.75,bcc\nTa0.25W0.75,bcc\nTa0.25Zr0.75,bcc\nTa0.5Ti0.5,bcc\nTa0.5V0.5,bcc\nTa0.5W0.5,bcc\nTa0.5Zr0.5,bcc\nTa0.75Ti0.25,bcc\nTa0.75V0.25,bcc\nTa0.75W0.25,bcc\nTa0.75Zr0.25,bcc\nTb0.25Th0.75,bcc\nTb0.25Y0.75,bcc\nTb0.5Th0.5,bcc\nTb0.5Y0.5,bcc\nTb0.75Th0.25,bcc\nTb0.75Y0.25,bcc\nTh0.25Zr0.75,bcc\nTh0.5Zr0.5,bcc\nTh0.75Zr0.25,bcc\nTi0.25U0.75,bcc\nTi0.25V0.75,bcc\nTi0.25W0.75,bcc\nTi0.25Zr0.75,bcc\nTi0.5U0.5,bcc\nTi0.5V0.5,bcc\nTi0.5W0.5,bcc\nTi0.5Zr0.5,bcc\nTi0.75U0.25,bcc\nTi0.75V0.25,bcc\nTi0.75W0.25,bcc\nTi0.75Zr0.25,bcc\nU0.25Zr0.75,bcc\nU0.5Zr0.5,bcc\nU0.75Zr0.25,bcc\nV0.1Zr0.9,bcc\nV0.25W0.75,bcc\nV0.5W0.5,bcc\nV0.75W0.25,bcc\nAg0.05Rh0.95,fcc\nAg0.25Au0.75,fcc\nAg0.25Pd0.75,fcc\nAg0.5Au0.5,fcc\nAg0.5Pd0.5,fcc\nAg0.65Cd0.35,fcc\nAg0.6Li0.4,fcc\nAg0.75Au0.25,fcc\nAg0.75Pd0.25,fcc\nAg0.7Zn0.3,fcc\nAg0.85In0.15,fcc\nAg0.85Zn0.15,fcc\nAg0.8Cd0.2,fcc\nAg0.8Li0.2,fcc\nAg0.8Mg0.2,fcc\nAg0.8Mn0.2,fcc\nAg0.8Pt0.2,fcc\nAg0.90Al0.10,fcc\nAg0.9Mg0.1,fcc\nAg0.9Mn0.1,fcc\nAg0.9Pt0.1,fcc\nAl0.05Co0.95,fcc\nAl0.08Pt0.92,fcc\nAl0.15Cu0.85,fcc\nAl0.1Ni0.9,fcc\nAl0.1Pd0.9,fcc\nAl0.25Co1Cr1Fe1Ni1,fcc\nAl0.375Co1Cr1Fe1Ni1,fcc\nAl0.3Co1Cr1Fe1Ni1,fcc\nAl0.8Zn0.2,fcc\nAl0.95Li0.05,fcc\nAl0.95Mg0.05,fcc\nAl0.9Zn0.1,fcc\nAu0.25Cu0.75,fcc\nAu0.25Pd0.75,fcc\nAu0.53V0.47,fcc\nAu0.5Cu0.5,fcc\nAu0.5Pd0.5,fcc\nAu0.71V0.29,fcc\nAu0.75Cu0.25,fcc\nAu0.7Fe0.3,fcc\nAu0.85Fe0.15,fcc\nAu0.85Li0.15,fcc\nAu0.85Pt0.15,fcc\nAu0.8Cr0.2,fcc\nAu0.8Ni0.2,fcc\nAu0.95Ta0.05,fcc\nAu0.9Cr0.1,fcc\nAu0.9Mn0.1,fcc\nAu0.9Nb0.1,fcc\nAu0.9Ni0.1,fcc\nAu0.9V0.1,fcc\nAu0.9Zn0.1,fcc\nCa0.25Sr0.75,fcc\nCa0.25Yb0.75,fcc\nCa0.5Sr0.5,fcc\nCa0.5Yb0.5,fcc\nCa0.75Sr0.25,fcc\nCo0.25Fe0.75,fcc\nCo0.25Ni0.75,fcc\nCo0.25Pd0.75,fcc\nCo0.25Pt0.75,fcc\nCo0.25Rh0.75,fcc\nCo0.2Ir0.8,fcc\nCo0.5Fe0.5,fcc\nCo0.5Ni0.5,fcc\nCo0.5Pd0.5,fcc\nCo0.5Pt0.5,fcc\nCo0.5Rh0.5,fcc\nCo0.75Fe0.25,fcc\nCo0.75Ni0.25,fcc\nCo0.75Pd0.25,fcc\nCo0.75Pt0.25,fcc\nCo0.75Rh0.25,fcc\nCo0.7Cr0.3,fcc\nCo0.85Cr0.15,fcc\nCo0.9Ga0.1,fcc\nCo0.9Ge0.1,fcc\nCo1.5Cr0.5Fe1Mn0.5Ni1,fcc\nCo1Cr0.75Fe1Mn0.75Ni1,fcc\nCo1Cr1.25Fe1Mn0.25Ni1,fcc\nCo1Cr1Fe0.5Mn0.5Ni1.5,fcc\nCo1Cr1Fe1Mn1Ni1,fcc\nCo1Cr1Fe1Mo0.1Ni1,fcc\nCo1Cr1Fe1Mo0.2Ni1,fcc\nCo1Cr1Fe1Ni1,fcc\nCo1Cr1Fe1Ni1Pd1,fcc\nCo1Cr1Fe1Ni1Pd2,fcc\nCo1Cr1Mn1Ni1,fcc\nCo1Cr1Ni1,fcc\nCo1Fe1Mn1Ni1,fcc\nCo1Fe1Ni1,fcc\nCo1Fe1Ni1Pd1,fcc\nCr0.1Rh0.9,fcc\nCr0.25Pt0.75,fcc\nCr0.2Rh0.8,fcc\nCr0.3Pd0.7,fcc\nCr0.5Pt0.5,fcc\nCr1Fe1Ni1,fcc\nCu0.1Rh0.9,fcc\nCu0.25Ni0.75,fcc\nCu0.25Pd0.75,fcc\nCu0.25Pt0.75,fcc\nCu0.5Mn0.5,fcc\nCu0.5Ni0.5,fcc\nCu0.5Pd0.5,fcc\nCu0.5Pt0.5,fcc\nCu0.75Mn0.25,fcc\nCu0.75Ni0.25,fcc\nCu0.75Pd0.25,fcc\nCu0.75Pt0.25,fcc\nCu0.85Li0.15,fcc\nCu0.8Rh0.2,fcc\nFe0.15Pt0.85,fcc\nFe0.25Ir0.75,fcc\nFe0.25Ni0.75,fcc\nFe0.25Pd0.75,fcc\nFe0.25Rh0.75,fcc\nFe0.5Ir0.5,fcc\nFe0.5Mn0.5,fcc\nFe0.5Ni0.5,fcc\nFe0.5Pd0.5,fcc\nFe0.75Ir0.25,fcc\nFe0.75Mn0.25,fcc\nFe0.75Ni0.25,fcc\nFe0.75Pd0.25,fcc\nFe0.75Rh0.25,fcc\nFe0.7Pt0.3,fcc\nFe0.85Pt0.15,fcc\nFe0.9Os0.1,fcc\nFe0.9Ru0.1,fcc\nIr0.25Ni0.75,fcc\nIr0.25Pt0.75,fcc\nIr0.25Rh0.75,fcc\nIr0.5Ni0.5,fcc\nIr0.5Pt0.5,fcc\nIr0.5Rh0.5,fcc\nIr0.75Ni0.25,fcc\nIr0.75Pt0.25,fcc\nIr0.75Rh0.25,fcc\nIr0.7Ru0.30,fcc\nIr0.85Ru0.15,fcc\nIr0.85W0.15,fcc\nIr0.8Mo0.2,fcc\nIr0.8Pd0.2,fcc\nIr0.95Ti0.05,fcc\nIr0.9Mo0.1,fcc\nIr0.9Nb0.1,fcc\nIr0.9Pd0.1,fcc\nIr0.9Ta0.1,fcc\nIr0.9V0.1,fcc\nMo0.15Pd0.85,fcc\nMo0.1Rh0.9,fcc\nMo0.3Pd0.7,fcc\nNb0.05Ni0.95,fcc\nNb0.1Rh0.9,fcc\nNd0.25Th0.75,fcc\nNd0.5Th0.5,fcc\nNd0.75Th0.25,fcc\nNi0.25Pd0.75,fcc\nNi0.25Pt0.75,fcc\nNi0.25Rh0.75,fcc\nNi0.5Pd0.5,fcc\nNi0.5Pt0.5,fcc\nNi0.5Rh0.5,fcc\nNi0.75Pd0.25,fcc\nNi0.75Pt0.25,fcc\nNi0.75Rh0.25,fcc\nNi0.75Zn0.25,fcc\nNi0.85Tc0.15,fcc\nNi0.85V0.15,fcc\nNi0.9Mo0.1,fcc\nNi0.9V0.1,fcc\nNi0.9W0.1,fcc\nNi0.9Zn0.1,fcc\nOs0.1Pt0.9,fcc\nOs0.1Rh0.9,fcc\nOs0.25Rh0.75,fcc\nOs0.2Pt0.8,fcc\nOs0.2Rh0.8,fcc\nOs0.45Rh0.55,fcc\nOs0.4Rh0.6,fcc\nPb0.25Tl0.75,fcc\nPb0.5Tl0.5,fcc\nPb0.75Tl0.25,fcc\nPd0.25Pt0.75,fcc\nPd0.25Rh0.75,fcc\nPd0.5Pt0.5,fcc\nPd0.5Rh0.5,fcc\nPd0.6V0.4,fcc\nPd0.75Pt0.25,fcc\nPd0.75Rh0.25,fcc\nPd0.8V0.2,fcc\nPr0.25Th0.75,fcc\nPr0.5Th0.5,fcc\nPr0.75Th0.25,fcc\nPt0.25Rh0.75,fcc\nPt0.5Rh0.5,fcc\nPt0.5Ru0.5,fcc\nPt0.6V0.4,fcc\nPt0.75Rh0.25,fcc\nPt0.75Ru0.25,fcc\nPt0.7Re0.3,fcc\nPt0.85Zn0.15,fcc\nPt0.85Zr0.15,fcc\nPt0.8Re0.2,fcc\nPt0.8V0.2,fcc\nPt0.9Re0.1,fcc\nRh0.7Ru0.3,fcc\nRh0.85Ru0.15,fcc\nRh0.9Ta0.1,fcc\nRh0.9V0.1,fcc\nRh0.9W0.1,fcc\nSc0.1Th0.9,fcc\nSc0.3Th0.7,fcc\nSc0.5Th0.5,fcc\nTb0.25Th0.75,fcc\nTb0.5Th0.5,fcc\nAl0.03Mg0.97,hcp\nAl0.03Sc0.97,hcp\nAl0.1Hf0.9,hcp\nAl0.1Ti0.9,hcp\nCd0.25Mg0.75,hcp\nCd0.5Mg0.5,hcp\nCd0.75Mg0.25,hcp\nCo0.25Os0.75,hcp\nCo0.25Re0.75,hcp\nCo0.25Ru0.75,hcp\nCo0.5Os0.5,hcp\nCo0.5Re0.5,hcp\nCo0.5Ru0.5,hcp\nCo0.75Os0.25,hcp\nCo0.75Re0.25,hcp\nCo0.75Ru0.25,hcp\nCo0.7Ir0.3,hcp\nCo0.8Rh0.2,hcp\nCo1Fe1Re1Ru1,hcp\nCr0.05Re0.95,hcp\nCr0.1Ir0.9,hcp\nCr0.25Ir0.75,hcp\nCr0.25Os0.75,hcp\nCr0.2Ru0.8,hcp\nCr0.3Rh0.7,hcp\nCr0.45Os0.55,hcp\nCr0.4Ir0.6,hcp\nCr0.4Rh0.6,hcp\nCr0.4Ru0.6,hcp\nCr0.5Ir0.5,hcp\nCr0.5Rh0.5,hcp\nDy1Gd1Ho1Tb1Y1,hcp\nDy1Gd1Lu1Tb1Tm1,hcp\nDy1Gd1Lu1Tb1Y1,hcp\nFe0.2Os0.8,hcp\nFe0.2Ru0.8,hcp\nFe0.5Os0.5,hcp\nFe0.5Ru0.5,hcp\nFe0.6Os0.4,hcp\nFe0.6Ru0.4,hcp\nGd1Ho1La1Tb1Y1,hcp\nHf0.25Sc0.75,hcp\nHf0.25Ti0.75,hcp\nHf0.25Zr0.75,hcp\nHf0.5Sc0.5,hcp\nHf0.5Ti0.5,hcp\nHf0.5Zr0.5,hcp\nHf0.75Sc0.25,hcp\nHf0.75Ti0.25,hcp\nHf0.75Zr0.25,hcp\nIr0.25Tc0.75,hcp\nIr0.2Ru0.8,hcp\nIr0.4Ru0.6,hcp\nIr0.5Mo0.5,hcp\nIr0.5Tc0.5,hcp\nIr0.5W0.5,hcp\nIr0.6W0.4,hcp\nIr0.7W0.3,hcp\nLi0.1Mg0.9,hcp\nMo0.07Re0.93,hcp\nMo0.1Rh0.9,hcp\nMo0.1Ru0.9,hcp\nMo0.1Ru0.9,hcp\nMo0.25Rh0.75,hcp\nMo0.25Ru0.75,hcp\nMo0.2Os0.8,hcp\nMo0.2Os0.8,hcp\nMo0.2Rh0.8,hcp\nMo0.2Ru0.8,hcp\nMo0.35Os0.65,hcp\nMo0.35Ru0.65,hcp\nMo0.3Os0.7,hcp\nMo0.3Rh0.7,hcp\nMo0.3Ru0.7,hcp\nMo0.4Rh0.6,hcp\nMo0.5Pd0.5,hcp\nMo0.5Rh0.5,hcp\nMo0.5Rh0.5,hcp\nMo1Pd1Rh1Ru1,hcp\nNb0.1Os0.9,hcp\nNb0.2Os0.8,hcp\nNi0.1Os0.9,hcp\nNi0.1Ru0.9,hcp\nNi0.1Tc0.9,hcp\nNi0.25Os0.75,hcp\nNi0.25Tc0.75,hcp\nNi0.2Ru0.8,hcp\nNi0.3Ru0.7,hcp\nNi0.4Tc0.6,hcp\nOs0.25Re0.75,hcp\nOs0.25Ru0.75,hcp\nOs0.5Re0.5,hcp\nOs0.5Ru0.5,hcp\nOs0.75Re0.25,hcp\nOs0.75Ru0.25,hcp\nOs0.7V0.3,hcp\nOs0.7W0.3,hcp\nOs0.85Rh0.15,hcp\nOs0.8Ta0.2,hcp\nOs0.8V0.2,hcp\nOs0.8W0.2,hcp\nOs0.9Ti0.1,hcp\nOs0.9V0.1,hcp\nOs0.9W0.1,hcp\nPt0.15Ru0.85,hcp\nPt0.1Re0.9,hcp\nPt0.25Re0.75,hcp\nPt0.35Re0.65,hcp\nPu0.1Sc0.9,hcp\nPu0.25Sc0.75,hcp\nRe0.25Ru0.75,hcp\nRe0.25Tc0.75,hcp\nRe0.5Ru0.5,hcp\nRe0.5Tc0.5,hcp\nRe0.75Ru0.25,hcp\nRe0.75Tc0.25,hcp\nRe0.9W0.1,hcp\nRh0.25Ru0.75,hcp\nRh0.25Tc0.75,hcp\nRh0.5Ru0.5,hcp\nRh0.5Tc0.5,hcp\nRh0.6W0.4,hcp\nRu0.7W0.3,hcp\nRu0.85Ta0.15,hcp\nRu0.8V0.2,hcp\nRu0.8W0.2,hcp\nRu0.9V0.1,hcp\nRu0.9W0.1,hcp\nSc0.25Y0.75,hcp\nSc0.25Zr0.75,hcp\nSc0.5Y0.5,hcp\nSc0.5Zr0.5,hcp\nSc0.75Y0.25,hcp\nSc0.75Zr0.25,hcp\nSm0.25Y0.75,hcp\nSm0.5Y0.5,hcp\nSm0.75Y0.25,hcp\nTb0.25Tm0.75,hcp\nTb0.25Y0.75,hcp\nTb0.5Tm0.5,hcp\nTb0.5Y0.5,hcp\nTb0.75Tm0.25,hcp\nTb0.75Y0.25,hcp\nTi0.25Zr0.75,hcp\nTi0.5Zr0.5,hcp\nTi0.75Zr0.25,hcp\nAgAs,multi-phase\nAgBe,multi-phase\nAgCo,multi-phase\nAgCr,multi-phase\nAgCu,multi-phase\nAgFe,multi-phase\nAgGe,multi-phase\nAgMn,multi-phase\nAgMo,multi-phase\nAgNi,multi-phase\nAgOs,multi-phase\nAgPb,multi-phase\nAgPt,multi-phase\nAgRe,multi-phase\nAgRh,multi-phase\nAgSb,multi-phase\nAgSi,multi-phase\nAgSn,multi-phase\nAgW,multi-phase\nAl0.25Co1Cr1Cu0.75Fe1Ni1,multi-phase\nAl0.25Co1Cr1Cu0.75Fe1Ni1Ti0.5,multi-phase\nAl0.25Cr1Cu1Fe1Ni2,multi-phase\nAl0.2Co1.5Cr1Fe1Ni1.5Ti0.5,multi-phase\nAl0.2Co1.5Cr1Fe1Ni1.5Ti1,multi-phase\nAl0.3Co1Cr1Cu1Fe1Ni1,multi-phase\nAl0.3Co1Cr1Fe1Mo0.1Ni1,multi-phase\nAl0.3Co1Cr1Fe1Ni1Ti0.1,multi-phase\nAl0.3Co1Cr2Fe1Ni1,multi-phase\nAl0.3Cr1Fe1.5Mn1Ni0.5,multi-phase\nAl0.3Cr1Fe1Ni1V1,multi-phase\nAl0.4Co1Cr1Fe1Mn1Ni1V1,multi-phase\nAl0.55V0.45,multi-phase\nAl0.5B0.2Co1Cr1Cu1Fe1Ni1,multi-phase\nAl0.5B0.6Co1Cr1Cu1Fe1Ni1,multi-phase\nAl0.5B1Co1Cr1Cu1Fe1Ni1,multi-phase\nAl0.5Ce1Co1Cu0.5Fe1Ni1Ti0.5,multi-phase\nAl0.5Co1Cr1Cu0.5Fe1Ni1,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1Ti0.8,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V0.2,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V0.4,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V0.6,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V0.8,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V1,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V1.2,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V1.4,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V1.6,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V1.8,multi-phase\nAl0.5Co1Cr1Cu1Fe1Ni1V2,multi-phase\nAl0.5Co1Cr1Fe1Ni1,multi-phase\nAl0.5Co1Cr1Fe1Ni1Ti1,multi-phase\nAl0.5Cr1Cu1Fe1Ni2,multi-phase\nAl0.5Cr1Fe1.5Mn1Ni0.5,multi-phase\nAl0.5Cr1Fe1Ni1Ti1V1,multi-phase\nAl0.5Cr1Fe1Ni1V1,multi-phase\nAl0.5Nb1Ta0.8Ti1.5V0.2Zr1,multi-phase\nAl0.5Nb1Ti1V1Zr1,multi-phase\nAl0.75Co1Cr1Cu0.25Fe1Ni1,multi-phase\nAl0.75Co1Cr1Cu0.25Fe1Ni1Ti0.5,multi-phase\nAl0.75Co1Cr1Fe1Ni1,multi-phase\nAl0.875Co1Cr1Fe1Ni1,multi-phase\nAl0.8Co1Cr1Cu1Fe1Ni1,multi-phase\nAl0.8Cr1Cu1Fe1Ni2,multi-phase\nAl0.8Cr1Fe1.5Mn1Ni0.5,multi-phase\nAl1.17Co1Cr1Fe1Ni1,multi-phase\nAl1.25Co1Cr1Fe1Ni1,multi-phase\nAl1.3Co1Cr1Cu1Fe1Ni1,multi-phase\nAl1.3Cr1Cu1Fe1Ni2,multi-phase\nAl1.5Co1Cr1Cu1Fe1Ni1,multi-phase\nAl1.5Co1Cr1Fe1Ni1,multi-phase\nAl1.5Co1Cr1Fe1Ni1Ti1,multi-phase\nAl1.5Cr1Cu1Fe1Ni2,multi-phase\nAl1.5Cr1Fe1.5Mn1Ni0.5,multi-phase\nAl1.5Cr1Fe1Mn1Ti1,multi-phase\nAl1.5Nb1Ti1V1Zr1,multi-phase\nAl1.8Co1Cr1Cu1Fe1Ni1,multi-phase\nAl1Au1Co1Cr1Cu1Ni1,multi-phase\nAl1Co0.5Cr0.5Fe0.5Mn1Ni1V0.5,multi-phase\nAl1Co0.5Cr0.5Fe0.5Mn1Ni1V1,multi-phase\nAl1Co0.5Cr1Cu1Fe1Ni1,multi-phase\nAl1Co0.5Cr1Fe1Mo0.5Ni1,multi-phase\nAl1Co1.5Cr1Fe1Mo0.5Ni1,multi-phase\nAl1Co1.5Cr1Fe1Ni1Ti0.5,multi-phase\nAl1Co1.5Cr2Fe1.5Mn2Ni1V1,multi-phase\nAl1Co1Cr0.5Cu1Fe1Ni1,multi-phase\nAl1Co1Cr0.5Fe1Mo0.5Ni1,multi-phase\nAl1Co1Cr1.5Fe1Mo0.5Ni1,multi-phase\nAl1Co1Cr1Cu0.25Fe1Ni1,multi-phase\nAl1Co1Cr1Cu0.25Fe1Ni1Ti0.5,multi-phase\nAl1Co1Cr1Cu0.5Fe1Ni1,multi-phase\nAl1Co1Cr1Cu0.5Fe1Ni1Ti0.5,multi-phase\nAl1Co1Cr1Cu0.5Ni1,multi-phase\nAl1Co1Cr1Cu1Fe0.5Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Mn1Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Mn1Ni1Ti1V1,multi-phase\nAl1Co1Cr1Cu1Fe1Mo0.2Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Mo0.4Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Mo0.6Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Mo0.8Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Mo1Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Ni0.5,multi-phase\nAl1Co1Cr1Cu1Fe1Ni1,multi-phase\nAl1Co1Cr1Cu1Fe1Ni1Si1,multi-phase\nAl1Co1Cr1Cu1Fe1Ni1Ti1,multi-phase\nAl1Co1Cr1Cu1Fe1Ni1Ti1V1,multi-phase\nAl1Co1Cr1Cu1Fe1Ni1V1,multi-phase\nAl1Co1Cr1Cu1Ni1,multi-phase\nAl1Co1Cr1Cu1Ni1Ti1Y0.5,multi-phase\nAl1Co1Cr1Cu1Ni1Ti1Y0.8,multi-phase\nAl1Co1Cr1Cu1Ni1Ti1Y1,multi-phase\nAl1Co1Cr1Fe0.6Mo0.5Ni1,multi-phase\nAl1Co1Cr1Fe1.5Mo0.5Ni1,multi-phase\nAl1Co1Cr1Fe1Mo0.1Ni1,multi-phase\nAl1Co1Cr1Fe1Mo0.2Ni1,multi-phase\nAl1Co1Cr1Fe1Mo0.3Ni1,multi-phase\nAl1Co1Cr1Fe1Mo0.4Ni1,multi-phase\nAl1Co1Cr1Fe1Mo0.5Ni1,multi-phase\nAl1Co1Cr1Fe1Nb0.1Ni1,multi-phase\nAl1Co1Cr1Fe1Nb0.25Ni1,multi-phase\nAl1Co1Cr1Fe1Nb0.5Ni1,multi-phase\nAl1Co1Cr1Fe1Nb0.75Ni1,multi-phase\nAl1Co1Cr1Fe1Ni1,multi-phase\nAl1Co1Cr1Fe1Ni1Si0.2,multi-phase\nAl1Co1Cr1Fe1Ni1Si0.4,multi-phase\nAl1Co1Cr1Fe1Ni1Si0.6,multi-phase\nAl1Co1Cr1Fe1Ni1Si0.8,multi-phase\nAl1Co1Cr1Fe1Ni1Si1,multi-phase\nAl1Co1Cr1Fe1Ni1Ti0.5,multi-phase\nAl1Co1Cr1Fe1Ni1Ti1,multi-phase\nAl1Co1Cr1Fe1Ni1Ti1.5,multi-phase\nAl1Co1Cr1Fe2Mo0.5Ni1,multi-phase\nAl1Co1Cr2Fe1Mo0.5Ni1,multi-phase\nAl1Co1Cu1Fe1Ni1,multi-phase\nAl1Co1Cu1Fe1Ni1Ti1,multi-phase\nAl1Co1Cu1Ni1,multi-phase\nAl1Co1Cu1Ni1Ti1Zn1,multi-phase\nAl1Co1Fe1Mn1Ni1,multi-phase\nAl1Co1Fe1Mo0.5Ni1,multi-phase\nAl1Co2Cr1Fe1Mo0.5Ni1,multi-phase\nAl1Co2Cr1Fe1Ni1Ti0.5,multi-phase\nAl1Co3Cr1Fe1Ni1Ti0.5,multi-phase\nAl1Cr0.5Cu1Fe1Ni1Ti1,multi-phase\nAl1Cr1.5Cu1Fe1Ni1Ti1,multi-phase\nAl1Cr1.5Nb1Ti1V1,multi-phase\nAl1Cr1Cu1Fe1Mn1Ni1,multi-phase\nAl1Cr1Cu1Fe1Ni1Ti1,multi-phase\nAl1Cr1Cu1Fe1Ni2,multi-phase\nAl1Cr1Fe1Mn1Ti0.25,multi-phase\nAl1Cr1Mo1Nb1Ti1,multi-phase\nAl1Cr1Mo1Si1Ti1,multi-phase\nAl1Cr1Nb1Ti1V1,multi-phase\nAl1Cr2Cu1Fe1Ni1Ti1,multi-phase\nAl1Cr3Cu1Fe1Ni1Ti1,multi-phase\nAl1Cu0.2Li0.5Mg1Zn0.5,multi-phase\nAl1Cu0.5Li0.5Mg1Sn0.2,multi-phase\nAl1Cu1Ni1,multi-phase\nAl1Fe1Mg1Ti1Zn1,multi-phase\nAl1Li0.5Mg1Sn0.2Zn0.5,multi-phase\nAl1Li1Mg1Sn1Zn1,multi-phase\nAl1Mo0.5Nb1Ta0.5Ti1Zr1,multi-phase\nAl1Nb1Ti1V1Zr1,multi-phase\nAl1Ti1V1Y1Zr1,multi-phase\nAl2.3Co1Cr1Cu1Fe1Ni1,multi-phase\nAl2.5Co1Cr1Cu1Fe1Ni1,multi-phase\nAl2.5Co1Cr1Fe1Ni1,multi-phase\nAl2.8Co1Cr1Cu1Fe1Ni1,multi-phase\nAl20Co10Cr10Cu10Fe10Mn10Ni10Ti10V10,multi-phase\nAl20Li20Mg10Sc20Ti30,multi-phase\nAl2Co1Cr1Cu1Fe1Ni1,multi-phase\nAl2Co1Cr1Fe1Ni1,multi-phase\nAl2Co1Cr1Fe1Ni1Ti1,multi-phase\nAl2Cr1Cu1Fe1Ni2,multi-phase\nAl2Cr1Fe1Mn1Ti0.25,multi-phase\nAl2Cr1Fe1Mn1Ti1,multi-phase\nAl3Co1Cr1Cu1Fe1Ni1,multi-phase\nAl3Co1Cr1Fe1Ni1,multi-phase\nAl3Cr1Cu1Fe1Ni2,multi-phase\nAl3Cr1Fe1Mn1Ti025,multi-phase\nAl40Co7.5Cr7.5Cu7.5Fe7.5Mn7.5Ni7.5Ti7.5V7.5,multi-phase\nAl4Cr1Fe1Mn1Ti0.25,multi-phase\nAl80Cu5Li5Mg5Zn5,multi-phase\nAl80Li5Mg5Sn5Zn5,multi-phase\nAlBa,multi-phase\nAlBe,multi-phase\nAlBi,multi-phase\nAlCa,multi-phase\nAlCd,multi-phase\nAlCr,multi-phase\nAlGa,multi-phase\nAlGe,multi-phase\nAlIn,multi-phase\nAlNb,multi-phase\nAlPb,multi-phase\nAlSe,multi-phase\nAlSi,multi-phase\nAlSn,multi-phase\nAlSr,multi-phase\nAlW,multi-phase\nAlYb,multi-phase\nAsCd,multi-phase\nAsCu,multi-phase\nAsMo,multi-phase\nAsPb,multi-phase\nAsPd,multi-phase\nAsTe,multi-phase\nAsTh,multi-phase\nAsZn,multi-phase\nAuBi,multi-phase\nAuCo,multi-phase\nAuCr,multi-phase\nAuMo,multi-phase\nAuPb,multi-phase\nAuSb,multi-phase\nAuSi,multi-phase\nAuTa,multi-phase\nAuTe,multi-phase\nAuW,multi-phase\nBaFe,multi-phase\nBaMg,multi-phase\nBaMo,multi-phase\nBaSc,multi-phase\nBaSn,multi-phase\nBaTi,multi-phase\nBaV,multi-phase\nBaY,multi-phase\nBe0.48Cu0.52,multi-phase\nBe0.4Co0.6,multi-phase\nBe1Cu1Ni1Ti1V1Zr1,multi-phase\nBeBi,multi-phase\nBeCr,multi-phase\nBeFe,multi-phase\nBeGa,multi-phase\nBeGe,multi-phase\nBeHf,multi-phase\nBeIn,multi-phase\nBeLi,multi-phase\nBeMg,multi-phase\nBeMo,multi-phase\nBeNb,multi-phase\nBeRu,multi-phase\nBeSi,multi-phase\nBeSr,multi-phase\nBeTa,multi-phase\nBeTh,multi-phase\nBeTh,multi-phase\nCaLa,multi-phase\nCaLi,multi-phase\nCaLu,multi-phase\nCaMg,multi-phase\nCaMo,multi-phase\nCaNa,multi-phase\nCaNd,multi-phase\nCaNi,multi-phase\nCaPt,multi-phase\nCaSb,multi-phase\nCaSc,multi-phase\nCaTi,multi-phase\nCaTm,multi-phase\nCaV,multi-phase\nCaY,multi-phase\nCdEu,multi-phase\nCdFe,multi-phase\nCdGa,multi-phase\nCdIn,multi-phase\nCdMo,multi-phase\nCdNa,multi-phase\nCdPb,multi-phase\nCdRb,multi-phase\nCdSn,multi-phase\nCdTl,multi-phase\nCdV,multi-phase\nCdZn,multi-phase\nCeCo,multi-phase\nCeCr,multi-phase\nCeFe,multi-phase\nCeHf,multi-phase\nCeIn,multi-phase\nCeIr,multi-phase\nCeLi,multi-phase\nCeMn,multi-phase\nCeMo,multi-phase\nCePu,multi-phase\nCeTa,multi-phase\nCeTi,multi-phase\nCeU,multi-phase\nCeV,multi-phase\nCeW,multi-phase\nCo0.56Cr0.44,multi-phase\nCo0.5Cr1Fe1Mn1.5Ni1,multi-phase\nCo1.5Cr1Fe1Mo0.1Ni1.5Ti0.5,multi-phase\nCo1.5Cr1Fe1Mo0.5Ni1.5Ti0.5,multi-phase\nCo1.5Cr1Fe1Mo0.8Ni1.5Ti0.5,multi-phase\nCo1.5Cr1Fe1Ni1.5Ti0.5,multi-phase\nCo1.5Cr1Fe1Ni1.5Ti1,multi-phase\nCo1Cr1Cu0.5Fe1Ni1,multi-phase\nCo1Cr1Cu1Fe1Mn1,multi-phase\nCo1Cr1Cu1Fe1Mn1Ni1,multi-phase\nCo1Cr1Cu1Fe1Mn1Ni1Ti1V1,multi-phase\nCo1Cr1Cu1Fe1Ni1,multi-phase\nCo1Cr1Cu1Fe1Ni1Ti0.5,multi-phase\nCo1Cr1Cu1Fe1Ni1Ti0.8,multi-phase\nCo1Cr1Cu1Fe1Ni1Ti1,multi-phase\nCo1Cr1Cu1Fe1Ni1Ti2,multi-phase\nCo1Cr1Fe1Ge1Mn1Ni1,multi-phase\nCo1Cr1Fe1Hf1Ni1,multi-phase\nCo1Cr1Fe1Mo0.3Ni1,multi-phase\nCo1Cr1Fe1Mo1Ni1,multi-phase\nCo1Cr1Fe1Nb1Ni1,multi-phase\nCo1Cr1Fe1Ni1Ta1,multi-phase\nCo1Cr1Fe1Ni1Ti0.3,multi-phase\nCo1Cr1Fe1Ni1Ti0.5,multi-phase\nCo1Cr1Fe1Ni1Ti1,multi-phase\nCo1Cr1Fe1Ni1V1,multi-phase\nCo1Cr1Fe1Ni1W1,multi-phase\nCo1Cr1Fe1Ni1Y1,multi-phase\nCo1Cr1Fe1Ni1Zr1,multi-phase\nCo1Cr1Mn1Ni1V1,multi-phase\nCo1Cr2Fe1Ni1,multi-phase\nCo1Cu1Fe1Ni1V1,multi-phase\nCo1Cu1Hf1Ti1Zr1,multi-phase\nCo1Fe1Ga1Mn1Ni1,multi-phase\nCo1Fe1Mn1Mo1Ni1,multi-phase\nCo1Fe1Mn1Ni1Sn1,multi-phase\nCo1Fe1Mn1Ni1V1,multi-phase\nCoDy,multi-phase\nCoEr,multi-phase\nCoGd,multi-phase\nCoIn,multi-phase\nCoLa,multi-phase\nCoLu,multi-phase\nCoNd,multi-phase\nCoPr,multi-phase\nCoSc,multi-phase\nCoSm,multi-phase\nCoTa,multi-phase\nCoTe,multi-phase\nCoW,multi-phase\nCoYb,multi-phase\nCr0.56Ni0.44,multi-phase\nCr1Cu1Fe1Mn1Ni1,multi-phase\nCr1Cu1Fe1Mn2Ni2,multi-phase\nCr1Cu1Fe1Mo1Ni1,multi-phase\nCr1Cu1Fe1Ni1Zr1,multi-phase\nCr1Cu1Fe1Ni2,multi-phase\nCr1Cu2Fe2Mn1Ni2,multi-phase\nCr1Cu2Fe2Mn2Ni1,multi-phase\nCr1Fe1.5Mn1Ni0.5,multi-phase\nCr1Fe1Mn1Ni1Ti1,multi-phase\nCr1Mo0.5Nb1Ta0.5Ti1Zr1,multi-phase\nCr1Nb1Ti1V1Zr1,multi-phase\nCr1Nb1Ti1Zr1,multi-phase\nCr2Cu1Fe2Mn1Ni1,multi-phase\nCr2Cu1Fe2Mn2Ni2,multi-phase\nCr2Cu2Fe1Mn2Ni2,multi-phase\nCr2Cu2Fe2Mn1Ni2,multi-phase\nCrCu,multi-phase\nCrHf,multi-phase\nCrMg,multi-phase\nCrNb,multi-phase\nCrSe,multi-phase\nCrTa,multi-phase\nCrTe,multi-phase\nCrY,multi-phase\nCrZr,multi-phase\nCsGa,multi-phase\nCsHf,multi-phase\nCsIn,multi-phase\nCsLi,multi-phase\nCsMg,multi-phase\nCsMo,multi-phase\nCsNa,multi-phase\nCsNb,multi-phase\nCsTa,multi-phase\nCsTe,multi-phase\nCsTl,multi-phase\nCsV,multi-phase\nCu1Fe1Hf1Ti1Zr1,multi-phase\nCuFe,multi-phase\nCuGa,multi-phase\nCuGe,multi-phase\nDyTa,multi-phase\nDyV,multi-phase\nDyW,multi-phase\nDyZr,multi-phase\nErFe,multi-phase\nErHf,multi-phase\nErMn,multi-phase\nErRe,multi-phase\nErRu,multi-phase\nErSn,multi-phase\nErTa,multi-phase\nErTi,multi-phase\nErV,multi-phase\nErW,multi-phase\nErZr,multi-phase\nEuFe,multi-phase\nEuLa,multi-phase\nEuMo,multi-phase\nEuRh,multi-phase\nEuTa,multi-phase\nEuV,multi-phase\nEuW,multi-phase\nFe0.4Mo0.6,multi-phase\nFe0.6Se0.4,multi-phase\nFeGa,multi-phase\nFeGd,multi-phase\nFeHf,multi-phase\nFeHo,multi-phase\nFeIn,multi-phase\nFeLa,multi-phase\nFeLi,multi-phase\nFeLu,multi-phase\nFeMg,multi-phase\nFeNa,multi-phase\nFeNb,multi-phase\nFePr,multi-phase\nFePu,multi-phase\nFeSb,multi-phase\nFeSc,multi-phase\nFeSm,multi-phase\nFeTa,multi-phase\nFeTb,multi-phase\nFeTh,multi-phase\nFeTm,multi-phase\nFeU,multi-phase\nFeY,multi-phase\nFeYb,multi-phase\nFeZn,multi-phase\nGaGe,multi-phase\nGaIn,multi-phase\nGaNa,multi-phase\nGaNb,multi-phase\nGaPb,multi-phase\nGaRb,multi-phase\nGaSn,multi-phase\nGaSr,multi-phase\nGaTl,multi-phase\nGaZn,multi-phase\nGdIn,multi-phase\nGdMn,multi-phase\nGdPb,multi-phase\nGdRe,multi-phase\nGdRu,multi-phase\nGdSn,multi-phase\nGdTi,multi-phase\nGdV,multi-phase\nGdW,multi-phase\nGdYb,multi-phase\nGdZr,multi-phase\nGeIn,multi-phase\nGeLu,multi-phase\nGeMn,multi-phase\nGeMo,multi-phase\nGeNb,multi-phase\nGePb,multi-phase\nGePb,multi-phase\nGeRe,multi-phase\nGeSb,multi-phase\nGeTi,multi-phase\nGeTl,multi-phase\nGeYb,multi-phase\nGeZn,multi-phase\nHfLi,multi-phase\nHfMn,multi-phase\nHfMo,multi-phase\nHfPu,multi-phase\nHfRb,multi-phase\nHfTh,multi-phase\nHfV,multi-phase\nHfY,multi-phase\nHoMn,multi-phase\nHoMo,multi-phase\nHoSn,multi-phase\nInMn,multi-phase\nInNb,multi-phase\nInRb,multi-phase\nInSi,multi-phase\nInSn,multi-phase\nInTa,multi-phase\nInV,multi-phase\nInZn,multi-phase\nIrNb,multi-phase\nIrPr,multi-phase\nIrRu,multi-phase\nIrTa,multi-phase\nKLi,multi-phase\nKMg,multi-phase\nKMo,multi-phase\nKNa,multi-phase\nKNb,multi-phase\nKTa,multi-phase\nKTi,multi-phase\nKV,multi-phase\nKZn,multi-phase\nKZr,multi-phase\nLaLi,multi-phase\nLaMn,multi-phase\nLaMo,multi-phase\nLaNb,multi-phase\nLaTa,multi-phase\nLaTi,multi-phase\nLaV,multi-phase\nLaW,multi-phase\nLiMn,multi-phase\nLiMo,multi-phase\nLiNa,multi-phase\nLiNi,multi-phase\nLiPr,multi-phase\nLiPu,multi-phase\nLiRb,multi-phase\nLiSb,multi-phase\nLiSe,multi-phase\nLiSi,multi-phase\nLiTa,multi-phase\nLiTe,multi-phase\nLiTi,multi-phase\nLiZr,multi-phase\nLuPb,multi-phase\nLuV,multi-phase\nLuW,multi-phase\nLuYb,multi-phase\nMgNa,multi-phase\nMgNb,multi-phase\nMgNi,multi-phase\nMgPb,multi-phase\nMgRb,multi-phase\nMgSb,multi-phase\nMgSn,multi-phase\nMgSr,multi-phase\nMgTh,multi-phase\nMgV,multi-phase\nMgYb,multi-phase\nMgZn,multi-phase\nMnMo,multi-phase\nMnNd,multi-phase\nMnPr,multi-phase\nMnPu,multi-phase\nMnSm,multi-phase\nMnSr,multi-phase\nMnTb,multi-phase\nMnY,multi-phase\nMoNd,multi-phase\nMoPa,multi-phase\nMoPb,multi-phase\nNb1Ti1V2Zr1,multi-phase\nOsPd,multi-phase\nOsPt,multi-phase\nOsPu,multi-phase\nOsTh,multi-phase\nOsU,multi-phase\nOsY,multi-phase\nOsYb,multi-phase\nPbPr,multi-phase\nPbPu,multi-phase\nPbSb,multi-phase\nPbSc,multi-phase\nPbSi,multi-phase\nPbSm,multi-phase\nPbSn,multi-phase\nPbTh,multi-phase\nPbZn,multi-phase\nPd0.4Si0.6,multi-phase\nPd0.4U0.6,multi-phase\nPd0.6Pu0.4,multi-phase\nPdRu,multi-phase\nPdW,multi-phase\nPmRh,multi-phase\nPmRu,multi-phase\nPmV,multi-phase\nPrPu,multi-phase\nPrTa,multi-phase\nPrTi,multi-phase\nPrU,multi-phase\nPrV,multi-phase\nPrW,multi-phase\nPtRe,multi-phase\nPtSr,multi-phase\nPtZn,multi-phase\nPuSm,multi-phase\nPuTa,multi-phase\nPuTi,multi-phase\nPuV,multi-phase\nRbTa,multi-phase\nRbTi,multi-phase\nRbTl,multi-phase\nRbV,multi-phase\nRbZn,multi-phase\nRe0.6Ti0.4,multi-phase\nReSb,multi-phase\nReSc,multi-phase\nReTb,multi-phase\nReTh,multi-phase\nReU,multi-phase\nReY,multi-phase\nReZr,multi-phase\nRh0.45Ta0.55,multi-phase\nRhU,multi-phase\nRuSn,multi-phase\nRuW,multi-phase\nSbSe,multi-phase\nSbSi,multi-phase\nSbZr,multi-phase\nScSr,multi-phase\nScU,multi-phase\nScV,multi-phase\nScW,multi-phase\nScW,multi-phase\nSiSn,multi-phase\nSiTa,multi-phase\nSiTe,multi-phase\nSiTl,multi-phase\nSiV,multi-phase\nSiW,multi-phase\nSiZn,multi-phase\nSmSn,multi-phase\nSmU,multi-phase\nSnTi,multi-phase\nSnV,multi-phase\nSnY,multi-phase\nSnZn,multi-phase\nSrTi,multi-phase\nSrV,multi-phase\nSrY,multi-phase\nTaTb,multi-phase\nTaTl,multi-phase\nTaTm,multi-phase\nTa_Th,multi-phase\n"
  },
  {
    "path": "dataset/Pei/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 1,\n   \"id\": \"16620829\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('pei.csv')\\n\",\n    \"# key=csv column name, value=slot in Q\\n\",\n    \"slot = {\\\"Alloy\\\":\\\"alloy\\\"}\\n\",\n    \"data_list = []\\n\",\n    \"for s in slot.keys():\\n\",\n    \"    for i, element in enumerate(df[s]):\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,2)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What is phase of given \\\"+ slot[s] + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write phase of given \\\"+ slot[s] + \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given \\\" + slot[s] + \\\", write its phase. ->\\\"\\n\",\n    \"        answer = df['Phase'][i]\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] =  \\\" \\\"+ element + \\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(answer)+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 2,\n   \"id\": \"9a79df0f\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 3,\n   \"id\": \"678932a4\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"data\": {\n      \"text/plain\": [\n       \"2325\"\n      ]\n     },\n     \"execution_count\": 3,\n     \"metadata\": {},\n     \"output_type\": \"execute_result\"\n    }\n   ],\n   \"source\": [\n    \"len(nouns)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 4,\n   \"id\": \"d7ace739\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"1252\\n\",\n      \"41\\n\",\n      \"['ticket', 'astronomy', 'coke', 'brush', 'granddaughter', 'turkey', 'roadway', 'oval', 'gallon', 'secure']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"print(len(data_list))\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add = int(len(data_list)/30)\\n\",\n    \"print(add)\\n\",\n    \"add_nouns = random.sample(nouns, add)\\n\",\n    \"print(add_nouns[:10])\\n\",\n    \"for an in add_nouns:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    ran2 = random.sample(list(slot.values()), 1)[0]\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What is phase of given \\\"+ ran2 + \\\"? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write phase of given \\\"+ ran2 + \\\". ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given \\\" + ran2 + \\\", write its phase. ->\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] = \\\" \\\"+ an + \\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" \\\"+an+\\\" does not have phase.\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\\n\",\n    \"random.shuffle(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 5,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('pei.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.8.0\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/Pei/pei.json",
    "content": "[\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ni0.9V0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Rh0.85Ru0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.95Ti0.05\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CeCo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" nigeria\\n\",\n        \"output\": \" nigeria does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.25Ni0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.5Os0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cu1Ni1Ti1Zn1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Fe1Mn1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" RbZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.85Tc0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GdYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.25Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sc0.5Th0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.75Co1Cr1Cu0.25Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.25Re0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CeU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.25Pd0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Fe1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pr0.25Th0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1.5Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.9Tc0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ru0.2Ti0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" EuRh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Fe1Ga1Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.8Pt0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Cu0.25Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Cu0.2Li0.5Mg1Zn0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.4Ir0.6\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pt0.9Re0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf1Nb1Ta1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pu0.25Sc0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" OsPt\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.75Ti0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" EuLa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PbSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.75Mo0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" LiSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.9V0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pu0.75Sc0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GaSr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Cr1.5Nb1Ti1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pb0.75Tl0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.75Ir0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr1Cu1Fe1Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" MnNd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cu1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cs0.75Rb0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.75Ti0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Fe1Mo0.3Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.75Ni0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.25Ru0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CeMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.08Pt0.92\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Re0.1V0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr2Cu1Fe2Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Fe1Ni1Pd1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Cr1Nb1Ti1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LuV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pu0.25Sc0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1.5Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.3Co1Cr1Fe1Mo0.1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.9Ru0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.5Nb1Ti1V1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FeY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.75Pt0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.15Ti0.85\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.25Ru0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cu0.25Pd0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Fe1Mo1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pt0.75Ru0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BeBi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.75Re0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AgAs\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.5Pd0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErRu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb1Ti1V1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pr0.75Th0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo1Pd1Rh1Ru1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AlSe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" InSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.9Ta0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.8Cd0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pt0.6V0.4\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo1Nb1Ta1Ti1V1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.8V0.2\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CoTe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.5Pd0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.1Hf0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Fe1Mo0.1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Au1Co1Cr1Cu1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr1Mo0.5Nb1Ta0.5Ti1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.55V0.45\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cu0.25Pt0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pd0.4Si0.6\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CsTl\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Fe1Mn1Mo1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mn0.5V0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CaLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.6Os0.4\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.5Fe0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Mo1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BeGa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cr1Mo1Nb1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Fe1Mn1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrTe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.8Mg0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.45Os0.55\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.1Os0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AsPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" HfY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" InNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CdPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.5Ir0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AgCo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" RbTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PmV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgCu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Sc0.75Zr0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" biology\\n\",\n        \"output\": \" biology does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CuGe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" MgTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.75Mn0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.02W0.98\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ta0.75Zr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" BeGe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.1Os0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pd0.75Rh0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.75Zr0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pr0.75Th0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.9Mg0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.95Rh0.05\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Y1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GaSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.7Ir0.3\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.3Cr0.7\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" MoPa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.5Ti0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.4Tc0.6\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" note\\n\",\n        \"output\": \" note does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Re0.25Tc0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.25Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.875Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.75Pd0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co0.5Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PuTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ru0.1Ta0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.25W0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" U0.75Zr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PbTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.25Ru0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" U0.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AsCd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LiNi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.75Pd0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.3Nb1Ta0.8Ti1.4V0.2Zr1.3\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SrTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" BaMg\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al4Cr1Fe1Mn1Ti0.25\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.7Cr0.3\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al2.5Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu0.5Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" OsTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" MgRb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CdSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ReY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Ti0.3\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" sneeze\\n\",\n        \"output\": \" sneeze does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.45Ta0.55\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.5Ti0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CdMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.8Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" RuW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" V0.25W0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AgBe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GdRe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" TaTb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CsGa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.7Tc0.3\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" ReTb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.2Co1.5Cr1Fe1Ni1.5Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.75Th0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" OsPu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CoTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.4Hf0.6Nb1Ta1Ti1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Si0.4\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" swiss\\n\",\n        \"output\": \" swiss does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.25Ru0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" OsPd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.9Re0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" SnTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GdPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgOs\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pt0.35Re0.65\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.2Ru0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.1Fe0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LiSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LuW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Tb0.5Y0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.75Co1Cr1Cu0.25Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Rh0.5Tc0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" change\\n\",\n        \"output\": \" change does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V1.4\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.1Rh0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CdRb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr0.5Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.85Rh0.15\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ba0.5Sr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al3Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Fe1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FePu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" SiZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CaMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ta0.75V0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" mark\\n\",\n        \"output\": \" mark does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CeW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" PrTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ca0.25Sr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Mo0.2Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AsPd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" KNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ag0.7Zn0.3\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pt0.8V0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Mn1Ni1Ti1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.5Mo0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cu1Hf1Ti1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ru0.9W0.1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.25V0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PrU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Tb0.25Y0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.2Co1.5Cr1Fe1Ni1.5Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cu0.1Rh0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.1Hf0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.25Ti0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Nb0.6Re0.4\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.25Re0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ScW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.2V0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PuV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FeGa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.8W0.2\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AgSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.5Ru0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" RhU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.7Pt0.3\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" PtZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" InSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" BaTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Sc0.1Th0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BaSc\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.9Mn0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.95Ta0.05\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" DyZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.2Fe0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PbSc\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pt0.1Re0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.75Ta0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GaIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.25Ti0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AgGe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.05Ta0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" PbPr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.75Fe0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" RbV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1.8Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Fe1Ge1Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Tb0.25Th0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.6Se0.4\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PrPu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Mo0.4Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.75Os0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GeTl\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Sc0.25Y0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GeMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CsLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sc0.75Y0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al80Cu5Li5Mg5Zn5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.1Ti0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo25.6Nb22.7Ta24.4W27.3\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" taxi\\n\",\n        \"output\": \" taxi does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.25Co1Cr1Cu0.75Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.93Si0.07\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" SmSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V0.8\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.6Ti0.4\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.85Li0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" InRb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.25W0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlBi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Fe0.5Mn0.5Ni1.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.9Nb0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SiW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.8Rh0.2\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1.3Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.5Rh0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" SrV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SbZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1.5Cr1Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" bee\\n\",\n        \"output\": \" bee does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.25Au0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" BeFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" roadway\\n\",\n        \"output\": \" roadway does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.2Os0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ScSr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ta0.25Ti0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1.17Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" SiSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1.5Cr1Fe1Ni1.5Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Mo0.3Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr0.5Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CoYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" MgSr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ag0.9Pt0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" cause\\n\",\n        \"output\": \" cause does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AlPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Cr1Fe1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pd0.5Rh0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al2.3Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AuSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.05Nb0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.85Pt0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo1Nb1Ta1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Dy1Gd1Lu1Tb1Tm1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.05Rh0.95\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" TaTl\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PdW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlSr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Cu2Fe2Mn2Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1.5Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.25Mo0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrSe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MgNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.2Rh0.8\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FePr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.25Ir0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1.5Cr1Fe1Ni1.5Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ScU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.75Ni0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb1Ti1V2Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Li0.85Mg0.15\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Tb0.5Th0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.5Re0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.75Pt0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.8Mn0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Au0.05Ti0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AsTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.75Re0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GeRe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgRe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1.5Cr1Fe1Mn1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SnY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GeNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Fe1Mn1Ni1Sn1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GeIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.9W0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V0.2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.15Pt0.85\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.4Rh0.6\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ag0.5Au0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.1Rh0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.5Pd0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.4Co1Cr1Fe1Mn1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.4Mo0.6\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CePu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pr0.5Th0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ru0.7W0.3\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.75Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Re0.5Ru0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Tb0.5Th0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Tb0.5Y0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cd0.75Mg0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.5Ti0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.9Ru0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Sc0.75Y0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.8Re0.2\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Sm0.75Y0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BeCr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CsTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.3Pd0.7\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LaTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.9Os0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PbSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GaNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Tb0.75Y0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" crowd\\n\",\n        \"output\": \" crowd does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.25Pt0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PmRu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pd0.6Pu0.4\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GePb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CsNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pt0.15Ru0.85\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Mn1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.5Pt0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CsIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V1.6\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ti0.5V0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ta0.25V0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PrTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.05Ti0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.9V0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" FeHf\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" PbSm\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CdZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ErSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ru0.8V0.2\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sm0.25Y0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pt0.8Re0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo1Nb1Ti1V1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.2Os0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sc0.3Th0.7\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" MgZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pd0.2V0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GeZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CoLa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Th0.75Zr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.25Zr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" skin\\n\",\n        \"output\": \" skin does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeRu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AgPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Re0.1Ta0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Ni1Ti1Y0.8\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CaNd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.5Pd0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.5W0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1.25Fe1Mn0.25Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Re0.4Ta0.6\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.25Ti0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Hf0.25Sc0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MgNi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CsNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Mn1Ni1Ti1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.05W0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ca0.85Yb0.15\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CaSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MgSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Si1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Th0.25Zr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AsZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.75Zn0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Fe1Mn1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cs0.25Rb0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" LiMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Sc0.25Y0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.7Fe0.3\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.95Os0.05\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ta_Th\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Os0.15Ta0.85\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CrZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Fe1Mg1Ti1Zn1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CeFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Fe1Nb1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Tb0.75Tm0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LuYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.5Rh0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.375Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Mo0.6Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Tb0.25Y0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CsMg\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" IrTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.25U0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Hf1Mo1Nb1Ti1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.5Ta0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AlGe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.75Pd0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" U0.25Zr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Hf1Nb1Ti1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" shallot\\n\",\n        \"output\": \" shallot does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.2Ti0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" FeTm\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.9Rh0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al3Cr1Fe1Mn1Ti025\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ni0.25Tc0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.4Ru0.6\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" EuW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.25Zr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ni0.5Rh0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GdSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.1W0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Nb1Ti1V1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SbSe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Li0.5Mg1Sn0.2Zn0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.3Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Cu1Fe1Mo1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" V0.75W0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AgSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.5Cr1Fe1Mn1.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ErHf\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.6W0.4\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ReSc\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.75Zr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.75Fe0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" InV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.05Ta0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.25V0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.5Cr1Fe1Ni1Ti1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pd0.8V0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Nd0.75Th0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.25Ta0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Ti1.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.15Cu0.85\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.2Ru0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" pastor\\n\",\n        \"output\": \" pastor does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.9Ge0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.1Ni0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.5Pt0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.1Ti0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.5Os0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LaMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.5Ti0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V1.8\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.8Tc0.2\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ca0.5Sr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Cr3Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CaLa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al2Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al2.8Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.8Zn0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.9Pd0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.3Co1Cr1Fe1Ni1Ti0.1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.75V0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ca0.75Sr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.98Pd0.02\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.5Pt0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.1Zr0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb1Ta1Ti1V1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" HfLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.4Ru0.6\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.25Zr0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.75Au0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.6Ru0.4\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.2Os0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Li0.5Mg0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Mo0.1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.03Sc0.97\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pt0.25Re0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.1Nb0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.5Ni0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sc0.75Ti0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.25Nb0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.25Ir0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AsMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.5Nb0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Fe1Nb0.25Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1.5Cr0.5Fe1Mn0.5Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" KMg\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.2Os0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" haircut\\n\",\n        \"output\": \" haircut does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.75Rh0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Au0.1Nb0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeMg\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" V0.5W0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" turkey\\n\",\n        \"output\": \" turkey does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.9Os0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.1Rh0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.9Ru0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.5Zr0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Ni1Ti1Y1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.9Ga0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cu0.5Pt0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MoPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CaY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.25Ta0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ca0.25Sr0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.8Ta0.2\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PbSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cu0.8Rh0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.75Zr0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrCu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.05Ta0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.9Rh0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AuBi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AlCd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr1Fe1.5Mn1Ni0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mn0.7V0.3\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pt0.5Ru0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" DyW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al3Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Dy1Gd1Lu1Tb1Y1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Au0.9Cr0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pu0.25Zr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CaMg\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" science\\n\",\n        \"output\": \" science does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.75Ta0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.75Ti0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" HfTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgRh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LaW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.05Co0.95\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cu1Fe1Hf1Ti1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.1Ta0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BaSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nd0.5Th0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AlSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al20Co10Cr10Cu10Fe10Mn10Ni10Ti10V10\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.25V0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CdFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GdV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.5Mn0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ReU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Au0.08V0.92\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al2Co1Cr1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" OsU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pr0.25Th0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" SnV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.25Pd0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" HfMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.3Rh0.7\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.8Li0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Nb0.25W0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.75Ru0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ta0.5Ti0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.75Ti0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.6W0.4\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ni0.25Os0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ba0.5Yb0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GaGe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" MgPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Re0.75Ru0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" KZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr1Mo1Nb1Re1Ta1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.1Rh0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.75V0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CuGa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.5V0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.4Rh0.6\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.8Ni0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.56Cr0.44\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr2Cu2Fe2Mn1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MoNd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Fe2Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ni0.75Pd0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AuTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.1Pt0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cr0.5Nb1Ti1V1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" EuFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" jewel\\n\",\n        \"output\": \" jewel does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.75Hf1Nb1Ta1Ti1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" V0.1Zr0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GaTl\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" MnMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.5Ru0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ag0.90Al0.10\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.25Co1Cr1Cu0.75Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.9W0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Si0.8\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ni0.75Pt0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" HoSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" LaNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AlNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al2Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pt0.25Rh0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo1Nb1Ta1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nd0.75Th0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" DyV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.45Rh0.55\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cr1Cu1Fe1Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CaPt\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Cu0.5Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Nb0.75Re0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" RuSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1.5Nb1Ti1V1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" HoMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.56Ni0.44\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.5Zr0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Os0.2Pt0.8\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MnTb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ca0.7Yb0.3\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ca0.5Yb0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PtSr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf1Nb1Ta1Ti1V1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CoLu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.1V0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mn0.25V0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Dy1Gd1Ho1Tb1Y1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Mn1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" PrV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ba0.25Eu0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Fe0.6Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.25Rh0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CeIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CeHf\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cu0.75Mn0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cr1Mo1Si1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pb0.25Tl0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Os0.75Ru0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" triangle\\n\",\n        \"output\": \" triangle does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Mn1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ba0.5Eu0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AuSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ni0.75Rh0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.5Fe0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cu0.75Ni0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Mo0.2Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pd0.1V0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" cabbage\\n\",\n        \"output\": \" cabbage does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BeHf\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" granddaughter\\n\",\n        \"output\": \" granddaughter does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.85Cr0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CsTe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.75Mn0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AuW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1.5Cr1Fe1Mo0.5Ni1.5Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.5Tc0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Ni1Ti0.8\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" FeSc\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.25Rh0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Li1Mg1Sn1Zn1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GdIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Li0.1Mg0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo1Nb1Re1Ta1Ti1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" HfRb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CsV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CeCr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CaLu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.5Ni0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ta0.25Zr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb1Ta1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" astronomy\\n\",\n        \"output\": \" astronomy does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.8Cr0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.3Rh0.7\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nd0.25Th0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.3Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.8Cr1Fe1.5Mn1Ni0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CdV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co0.5Cr1Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GdTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GaRb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LiTe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CdIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" burst\\n\",\n        \"output\": \" burst does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Ni1Ti2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.9V0.1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GdRu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Cr1.5Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.5V0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AuMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Th0.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Re0.25Ru0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.85In0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.9W0.1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.75Nb0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ni0.9Mo0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeLa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Si0.6\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pt0.5Rh0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Nb1Ta1Ti1V1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Nb1.5Ta0.5Ti1.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1.25Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Rh0.9Ta0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Fe1Mn1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CeMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al2Cr1Fe1Mn1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ta0.5V0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.75Re0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ba0.25Sr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" teaching\\n\",\n        \"output\": \" teaching does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" yogurt\\n\",\n        \"output\": \" yogurt does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pu0.75Zr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.8Pd0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" KLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr1Nb1Ti1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.9Mo0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Fe1Hf1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Fe1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.4Zr0.6\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.25Rh0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LaTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" KMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.25Zr0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Mo1Nb1Ta1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" oval\\n\",\n        \"output\": \" oval does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LaV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MgYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ScV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu0.25Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.75W0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.25Tc0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.05Ni0.95\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1.5Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CoDy\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.25Tc0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5B1Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cr1Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" PbPu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.8V0.2\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.71V0.29\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pu0.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.25Ti0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Fe1Ni1W1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" asparagus\\n\",\n        \"output\": \" asparagus does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.9Zn0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Re0.1Ti0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.25Rh0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ba0.75Ca0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MgNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.25Os0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cu0.75Pd0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GeLu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Tb0.25Tm0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.7V0.3\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pu0.5Sc0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" LiNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.1Cr0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cu0.5Pd0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PuSm\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ba0.25Eu0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1.5Cr1Fe1Mo0.8Ni1.5Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CoNd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AlBa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CeTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" IrPr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.25Cu0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.75Ta0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Tb0.75Y0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CaNi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ba0.75Sr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Pd2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.5Ru0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.9Mn0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" PuTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Rh0.7Ru0.3\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" MnY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FeHo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FeIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1.5Cr2Fe1.5Mn2Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CdEu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ScW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ba0.75Eu0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb1Ta1Ti1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.1Tc0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.25Os0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.4Rh0.6\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.2Ru0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.5Rh0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.6Li0.4\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.25V0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Cr1Mo1Ti1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Sm0.25Y0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ReZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" OsYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LiZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.5W0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ni0.25Pt0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" dish\\n\",\n        \"output\": \" dish does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.9W0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo21.7Nb20.6Ta15.6V21W21.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AgNi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Gd1Ho1La1Tb1Y1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cu1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ba0.5Eu0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Fe1Mn1Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CoIn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PdRu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.3Co1Cr2Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.1Ru0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.5Nb0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.05Re0.95\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" secure\\n\",\n        \"output\": \" secure does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" HfPu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ti0.5W0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.95Li0.05\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co3Cr1Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CaNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.25Pd0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Nb0.9Os0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FeU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.75Rh0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CsHf\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.3Cr1Fe1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.1Ru0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ReTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" security\\n\",\n        \"output\": \" security does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.75Ni0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.5Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.25Fe0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.8Pd0.2\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Nb1Ti1V1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Mo0.5Nb1Ta0.5Ti1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ba0.5Ca0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AgCr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sc0.5Y0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.65Cd0.35\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ru0.85Ta0.15\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" FeZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Tb0.5Tm0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr1Cu2Fe2Mn1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pt0.85Zr0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.95Ir0.05\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" EuV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GaNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GePb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.5Re0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ru0.1Ti0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pt0.75Rh0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.9Ga0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AlBe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sc0.5Y0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BaV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.95Mg0.05\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.35Ru0.65\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" DyTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CsMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.25Pd0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pt0.05V0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1.5Cr1Fe1Mo0.1Ni1.5Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CaV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Re0.2Ta0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5Cr1Fe1.5Mn1Ni0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GeMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" SmU\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu0.5Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Re0.9W0.1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ca0.75Sr0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Nb0.1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.25Ti0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pd0.5Pt0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MnPu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" GeTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sm0.75Y0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.75Zr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.5Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ReSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.8Mo0.2\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" russia\\n\",\n        \"output\": \" russia does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.5Cu0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BaMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LiMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LiRb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CoW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" SrY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.75W0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlSn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.9Ti0.1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.5Rh0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo1Nb1Ta1V1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Au0.53V0.47\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Rh0.9V0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Fe1Ni1Si0.2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeGd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AlCr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.25Ni0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Hf0.5Sc0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GdZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.25Zr0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cd0.5Mg0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.85Fe0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" KNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ErTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.1W0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.7Ru0.30\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" SiTe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ba0.25Yb0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AuPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" HoMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" BeLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.8Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" FeTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CoGd\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CdNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ag0.85Zn0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeMg\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AsTe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CoPr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Nb0.75Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cu1Fe1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.7W0.3\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ta0.25W0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" coke\\n\",\n        \"output\": \" coke does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LaMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Fe1Mo0.2Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Mo0.4Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.5Ti0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.5Ta0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" RbTl\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al2.5Co1Cr1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.75V0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ta0.5W0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LaLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FeTb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.5Rh0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PmRh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrMg\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5Co1Cr1Cu0.5Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CoSc\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr2Cu2Fe1Mn2Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ru0.2Ta0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nd0.25Th0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.5Ni0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1.5Cr1Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CeLi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pt0.7Re0.3\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" AgSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" SiV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ba0.75Eu0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pd0.6V0.4\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Mo0.8Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5B0.2Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Nb1Ti1V1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5B0.6Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Hf0.75Sc0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CdTl\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pb0.5Tl0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CdGa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" InZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GdW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sc0.2Zr0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Ni1Ti1Y0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mn0.6V0.4\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.2W0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Fe1.5Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Be1Cu1Ni1Ti1V1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.5Mn0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V0.4\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1.5Cr1Fe1.5Mn1Ni0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AuCo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SiTl\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Fe1Re1Ru1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AsCu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ru0.1W0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" ErRe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SiTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pt0.85Zn0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Pd1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.1Rh0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.5Ir0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Cu1Fe1Ni1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CeTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GaZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pr0.5Th0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.5Pd0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GeSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Li0.35Mg0.65\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" HfV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Fe0.85Pt0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ru0.2W0.8\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co0.5Cr0.5Fe0.5Mn1Ni1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CeV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Be0.48Cu0.52\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MgSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.25Ti0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.5Pd0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PrW\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeLu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" KZr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.9Zn0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sm0.5Y0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CoEr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Hf1Nb1Ti1V1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.1Pd0.9\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al80Li5Mg5Sn5Zn5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.1Ir0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.1V0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ti0.75Zr0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V1.2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.35Os0.65\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cr1Fe1Mn1Ti0.25\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ru0.9V0.1\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V0.6\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" GdMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.5V0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr1Fe1Ni1Ta1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Sm0.5Y0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1V2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pu0.1Sc0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Ni1Si1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.15Cr0.85\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SnZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.25Th0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Pd0.4U0.6\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.5Nb1Ta0.8Ti1.5V0.2Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Fe1Nb0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.85W0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.2Ru0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co1Cr0.75Fe1Mn0.75Ni1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ru0.8W0.2\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" OsY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AuTe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.3Ru0.7\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ti0.5Zr0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.05Mo0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ni0.85V0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.25Zr0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co0.5Cr0.5Fe0.5Mn1Ni1V0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" HfMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CuFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CaSc\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.7W0.3\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GeYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CeIr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Ni0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cd0.25Mg0.75\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.25W0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo1Nb1Re1Ta1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MnPr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ir0.5Pt0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cu0.25Ni0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Cr0.5Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu1Fe1Ni1Ti1V1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ag0.05Zr0.95\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" ticket\\n\",\n        \"output\": \" ticket does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" LuPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ta0.75Ti0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" EuTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ba0.25Ca0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Au0.9Nb0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.9Ni0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.5Ta0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Be0.4Co0.6\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" SbSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" banker\\n\",\n        \"output\": \" banker does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.25Pd0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.25Rh0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" GaPb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlCa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Os0.15Ti0.85\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.5Tc0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nd0.5Th0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" EuMo\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo0.3Os0.7\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.2Rh0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co1Cr1Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co2Cr1Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" BeTh\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al0.4V0.6\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Fe0.85Zn0.15\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" skill\\n\",\n        \"output\": \" skill does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pd0.25Rh0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" IrRu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" CaTm\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" KTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ni0.3Ru0.7\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" FeSb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Hf0.75Nb0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Co1Cr1Cu0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cs0.5Rb0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Co0.75Rh0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CaTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Os0.25Rh0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" InMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BeSi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al2Cr1Fe1Mn1Ti0.25\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LiTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Cr2Cu1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Nb1Re1Ta1Ti1V1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Co2Cr1Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.1Ru0.9\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" LiPu\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" LiPr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ta0.75W0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1.5Co1Cr1Fe1Ni1Ti1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Au0.75Cu0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" CrHf\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" RbTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" InTa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LiSe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.07Re0.93\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cu0.75Pt0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ca0.25Yb0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" gallon\\n\",\n        \"output\": \" gallon does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AuCr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cu0.85Li0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al3Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" TaTm\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.5U0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cu0.5Mn0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ca0.5Sr0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.3Pd0.7\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MnSr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Fe0.25Ni0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf0.25Nb0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al1Ti1V1Y1Zr1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" KTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ga0.15Ti0.85\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.5Ce1Co1Cu0.5Fe1Ni1Ti0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" FeNa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cr0.2Ru0.8\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Co0.2Ir0.8\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al2Co1Cr1Cu1Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Ti0.75W0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" brush\\n\",\n        \"output\": \" brush does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Hf1Nb1Ta1Ti1Zr1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al40Co7.5Cr7.5Cu7.5Fe7.5Mn7.5Ni7.5Ti7.5V7.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ti0.75U0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AgPt\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlYb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" IrNb\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ba0.75Yb0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" sea\\n\",\n        \"output\": \" sea does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Be0.02W0.98\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" MgV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Re0.75Tc0.25\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr0.2Rh0.8\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Nb0.25Ta0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Mo0.9Re0.1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" PtRe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1.3Cr1Cu1Fe1Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Nb0.5W0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ta0.5Zr0.5\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Pd0.75Pt0.25\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.25Fe0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ni0.9Zn0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co0.25Pt0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Tb0.25Th0.75\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.9Pd0.1\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Rh0.1V0.9\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.3Cr1Fe1.5Mn1Ni0.5\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr1Cu1Fe1Mn2Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Os0.5Ru0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Cu0.5Ni0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al20Li20Mg10Sc20Ti30\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Nb0.65Ru0.35\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" FeSm\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" BeSr\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo0.15Pd0.85\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Mo1Nb1Ta1Ti1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Sc0.5Th0.5\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" AlGa\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Pd0.25Pt0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Co1Cr2Fe1Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al1Cu0.5Li0.5Mg1Sn0.2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Re0.4Ti0.6\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.5Mo0.5\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Ir0.85Ru0.15\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Al0.03Mg0.97\\n\",\n        \"output\": \" hcp\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" PbZn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" BaFe\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" AgMn\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Al1Co1Cr2Fe1Mo0.5Ni1\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" LiTi\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Al0.5Co1Cr1Cu1Fe1Ni1Ti0.8\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" invoice\\n\",\n        \"output\": \" invoice does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" KV\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Cr0.85Ru0.15\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Cr2Cu1Fe2Mn2Ni2\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" Tb0.75Th0.25\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" Mo1Nb1Re1Ta1V1W1\\n\",\n        \"output\": \" bcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" BaY\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"Write phase of given alloy. ->\",\n        \"input\": \" CoSm\\n\",\n        \"output\": \" multi-phase\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" turret\\n\",\n        \"output\": \" turret does not have phase.\\n\"\n    },\n    {\n        \"instruction\": \"Given alloy, write its phase. ->\",\n        \"input\": \" Ir0.25Pt0.75\\n\",\n        \"output\": \" fcc\\n\"\n    },\n    {\n        \"instruction\": \"What is phase of given alloy? ->\",\n        \"input\": \" MnSm\\n\",\n        \"output\": \" multi-phase\\n\"\n    }\n]"
  },
  {
    "path": "dataset/Polar Metals Materials Database/MTD.csv",
    "content": "Material,Space group,Point group,Structure Type,Polar structural phase transition,Superconducting transition,Magnetic ordering transition,Subclass,Reference (DOI)\r\nBaTiO3 (La-doped),P4mm,4mm,perovskite,Yes,,,DDF,10.1038/s41598-017-04635-3\r\nBaTiO3-d,P4mm,4mm,perovskite,Yes,,,DDF,10.1103/PhysRevLett.104.147602\r\nPbTiO3-d,P4mm,4mm,perovskite,P,,,EPM,10.1103/PhysRevB.94.224107\r\nPbTi(1-x)NbxO3,P4mm,4mm,perovskite,,,,EPM,10.1103/PhysRevB.96.165206\r\nBiFeO3-d,R3c,3m,perovskite,P,,Yes,EPM,10.1103/PhysRevB.93.174110\r\nSr(1-x)CaxTiO3-d,P4mm,4mm,perovskite,Yes,Yes,,DPM,10.1038/NPHYS4085\r\nBaMnO3 (n-doped),Amm2,mm2,perovskite,P,,,EPM,10.1103/PhysRevB.97.054107\r\nBiAlO3 (n-doped),P4mm,4mm,perovskite,P,,,EPM,10.1103/PhysRevB.97.054107\r\nBaTiO3/SrTiO3/LaTiO3,mm4*,4mm,perovskite,,,,IPM,10.1038/s41467-018-03964-9\r\nLaAlO3/Ba0.2Sr0.8TiO3/SrTiO3,unknown,unknown,perovskite,,,,IPM,10.1038/s42005-019-0227-4\r\nLaFeO3/YFeO3 (n-doped),Pmc2_1,mm2,perovskite,P,,,IPM,10.1103/PhysRevB.97.054107\r\nNdNiO3 on (111) LaAlO3,Pc,m,perovskite,,,,PM,10.1038/nature17628\r\nLaNiO3 on (111) LaAlO3,Pc,m,perovskite,,,,PM,10.1038/nature17628\r\nLiOsO3,R3c,3m,LiNbO3-type,Yes,,,DPM,10.1038/NMAT3754\r\nLiNbO3 (n-doped),R3c,3m,LiNbO3-type,P,,,DDF,10.1103/PhysRevMaterials.3.054405\r\nMgReO3,R3c,3m,LiNbO3-type,P,,,PM,10.1103/PhysRevB.90.094108\r\nTiGaO3,R3c,3m,LiNbO3-type,P,,,PM,10.1103/PhysRevB.90.094108\r\nCa3Ru2O7,Bb2_1m,mm2,Ruddlesden-Popper,,,Yes,PM,10.1021/acs.nanolett.8b00633\r\n\"(Sr,Ca)Ru2O6\",Pmc2_1,mm2,perovskite,P,,Yes,PM,10.1088/0953-8984/26/26/265501\r\nBi5Ti5O17,Pm2_1n,mm2,layered perovskite,P,,,APM,10.1038/ncomms11211\r\nBiPbTi2O6,Pmm2,mm2,post-perovskite,P,,,PM,10.1038/s43246-019-0005-6\r\nLa2Ti2O7 (n-doped),P2_1,2,layered perovskite,P,,,EPM,10.1103/PhysRevB.97.054107\r\nSr2Nb2O7 (n-doped),Cmc2_1,mm2,layered perovskite,P,,,EPM,10.1103/PhysRevB.97.054107\r\nMgCNi3,P4mm,4mm,BaNiSn3-type,P,,,PM,10.1103/PhysRevMaterials.2.125004\r\nZnCNi3,P4mm,4mm,BaNiSn3-type,P,,,PM,10.1103/PhysRevMaterials.2.125004\r\nCdCNi3,P4mm,4mm,BaNiSn3-type,P,,,PM,10.1103/PhysRevMaterials.2.125004\r\nCeSiPt3,P4mm,4mm,antiperovskite,,Yes,Yes,PM,10.1103/PhysRevLett.92.027003\r\nLiGaGe,P6_3mc,6mm,LiGaGe-type,,,,PM,10.1103/PhysRevB.99.195154\r\nSrHgPb,P6_3mc,6mm,LiGaGe-type,P,,,PM,10.1103/PhysRevLett.121.106404\r\nSrHgSn,P6_3mc,6mm,LiGaGe-type,P,,,PM,10.1103/PhysRevLett.121.106404\r\nCaHgSn,P6_3mc,6mm,LiGaGe-type,P,,,PM,10.1103/PhysRevLett.121.106404\r\nKMgSb0.2Bi0.8,P6_3mc,6mm,LiGaGe-type,P,,,PM,10.1103/PhysRevLett.117.076401\r\nCaAgBi,P6_3mc,6mm,LiGaGe-type,P,,,PM,10.1103/PhysRevMaterials.1.044201\r\nLiZnBi,P6_3mc,6mm,LiGaGe-type,P,,,PM,10.1103/PhysRevB.96.115203\r\nLaAuGe,P6_3mc,6mm,LiGaGe-type,,,,PM,10.1063/1.5132339\r\nLaPtSb,P6_3mc,6mm,LiGaGe-type,,,,PM,10.1063/1.5132339\r\nWTe2,Pnm2_1,mm2,2D,Yes,Yes,,APM,10.1038/s41586-018-0336-3\r\nMoTe2,Pnm2_1,mm2,2D,Yes,,,PM,10.1126/sciadv.1601378\r\nCrN,6mm*,6mm,2D,,,Yes,APM,10.1103/PhysRevB.96.235415\r\nCrB2,6mm*,6mm,2D,P,,Yes,APM,10.1103/PhysRevB.96.235415\r\nFeb-02,6mm*,6mm,2D,,,,APM,10.1021/acs.nanolett.6b02335\r\nP,P6_3mc,6mm,α-La-like,P,,,PM,10.1088/1361-648X/aadeaa\r\nAs,P6_3mc,6mm,α-La-like,P,,,PM,10.1088/1361-648X/aadeaa\r\nSb,P6_3mc,6mm,α-La-like,P,,,PM,10.1088/1361-648X/aadeaa\r\nBi,P6_3mc,6mm,α-La-like,P,,,PM,10.1088/1361-648X/aadeaa\r\nSnP,I4mm,4mm,rock salt,Yes,Yes,,DPM,10.1103/PhysRevLett.119.207001\r\nPdBi,P2_1,2,PdBi-type,,Yes,,PM,10.1016/j.phpro.2013.04.062\r\nUIr,P2_1,2,PdBi-type,,Yes,Yes,PM,10.1007/978-3-642-24624-1_2\r\nLaNiC2,Amm2,mm2,CeNiC2-type,,Yes,Yes,PM,10.1016/j.physc.2014.01.008\r\nNdRhC2,Amm2,mm2,CeNiC2-type,,,Yes,PM,10.1021/cm00006a007\r\nPrRhC2,Amm2,mm2,CeNiC2-type,,,Yes,PM,10.1021/cm00006a007\r\nLaSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nCeSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nPrSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nNdSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nPmSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nSmSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nEuSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nGdSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nTbSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nDySr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nHoSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nErSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nTmSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nYbSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nYSr2Cu2GaO7,Ima2,mm2,LnSr2Cu2GaO7,,Yes,Yes,PM,10.1021/cm00017a032\r\nV2Hf,Imm2,mm2,Laves phase,Yes,Yes,,DPM,10.1103/PhysRevB.17.1136\r\nLi2IrSi3,P3_1c,3m,kagome,,Yes,,PM,10.7566/JPSJ.83.093706\r\nMg2Al3,R3m,3m,Samson phase,Yes,Yes,,DPM,10.1103/PhysRevB.76.014528\r\nLa5B2C6,P4,4,La5B2C6-type,,Yes,,PM,10.1016/0022-5088(83)90520-9\r\nBaPtSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1103/PhysRevB.80.064504\r\nCeIrSi3,I4mm,4mm,BaNiSn3-type,,Yes,Yes,PM,10.1143/JPSJS.77SA.37\r\nCeRhSi3,I4mm,4mm,BaNiSn3-type,,Yes,Yes,PM,10.1143/JPSJ.76.051010\r\nLaPtSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1103/PhysRevB.89.094509\r\nLaPdSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1103/PhysRevB.89.094509\r\nCeIrGe3,I4mm,4mm,BaNiSn3-type,,Yes,Yes,PM,10.1016/j.jmmm.2006.10.151\r\nEuNiGe3,I4mm,4mm,BaNiSn3-type,,,Yes,PM,10.1103/PhysRevB.87.064406\r\nLaRhGe3,I4mm,4mm,BaNiSn3-type,,,,PM,10.1063/5.0042924\r\nIrRhGe3,I4mm,4mm,BaNiSn3-type,,,,PM,10.1063/5.0042924\r\nPdRhGe3,I4mm,4mm,BaNiSn3-type,,,,PM,10.1063/5.0042924\r\nSrPdGe3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1088/1742-6596/273/1/012078\r\nSrPtGe3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1088/1742-6596/273/1/012078\r\nPrPdIn2,I4mm,4mm,HfNiGa2-Type,,,Yes,PM,10.1021/cm031139m\r\nCePt3Si,I4mm,4mm,anti-perovskite,,Yes,Yes,PM,10.1103/PhysRevLett.92.027003\r\nLi2(Pd1-xPtx)3B,I4mm,4mm,Li2(Pd1-xPtx)3B,,Yes,Yes,PM,10.1088/1742-6596/400/2/022096\r\nKCu7P3,P31m,3m,2D,,,,PM,10.1021/acs.inorgchem.9b01336\r\nBi2FeCrO6,R3,3,perovskite,P,,Yes,PM,10.1103/PhysRevLett.123.107201\r\nCeAuGe,P6_3mc,6mm,AlB2-type,,,Yes,PM,10.1016/0304-8853(95)00430-0\r\nLuAuGe,P6_3mc,6mm,AlB2-type,,,,PM,10.1016/0925-8388(95)02069-1\r\nScAuGe,P6_3mc,6mm,AlB2-type,,,,PM,10.1016/0925-8388(95)02069-1\r\nHoAuGe,P6_3mc,6mm,NdPtSb-type,,,Yes,PM,10.1088/0953-8984/13/11/315\r\nCeCuSn,P6_3mc,6mm,AlB2-type,,,,PM,10.1016/j.jallcom.2004.09.086\r\nLa15Ge9C,P6_3mc,6mm,La15Ge9Fe-type,,,,PM,10.1016/j.jallcom.2011.03.092\r\nLa15Ge9Fe,P6_3mc,6mm,Mn5Si3-type,,,Yes,PM,10.1021/ic9515158\r\nLa15Ge9Co,P6_3mc,6mm,Mn5Si3-type,,,,PM,10.1021/ic9515158\r\nLa15Ge9Ni,P6_3mc,6mm,Mn5Si3-type,,,,PM,10.1021/ic9515158\r\nSr3Cu8Sn4,P6_3mc,6mm,BaAl4-type,,,,PM,10.1016/j.intermet.2011.02.018\r\nIrMg2.03In.97,P6_3mc,6mm,FeGa3-type,,,,PM,10.1016/j.intermet.2003.12.001\r\nIrMg2.20In.80,P6_3mc,6mm,FeGa3-type,,,,PM,10.1016/j.intermet.2003.12.001\r\nCaAlSi,P6_3,6,MgB2-Type,,Yes,,PM,10.1143/JPSJ.75.043713\r\nTlV6S8,P6_3,6,Nb3Te4-type,,Yes,,PM,10.1016/S0038-1098(01)00333-7\r\nKV6S8,P6_3,6,Nb3Te4-type,,Yes,,PM,10.1016/S0038-1098(01)00333-7\r\nRbV6S8,P6_3,6,Nb3Te4-type,,Yes,,PM,10.1016/S0038-1098(01)00333-7\r\nCsV6S8,P6_3,6,Nb3Te4-type,,Yes,,PM,10.1016/S0038-1098(01)00333-7\r\nLaPt3B,P4mm,4mm,anti-perovskite,,,Yes,PM,10.1016/S0925-8388(03)00373-6\r\nPrPt3B,P4mm,4mm,anti-perovskite,,,Yes,PM,10.1016/S0925-8388(03)00373-6\r\nNdPt3B,P4mm,4mm,anti-perovskite,,,Yes,PM,10.1016/S0925-8388(03)00373-6\r\nLaRhSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1016/0025-5408(84)90017-5\r\nLaIrSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1016/0025-5408(84)90017-5\r\nCeCoGe3,I4mm,4mm,BaNiSn3-type,,Yes,Yes,PM,10.1016/j.jmmm.2006.10.717\r\nLaCoGe3,I4mm,4mm,BaNiSn3-type,,,Yes,PM,10.1143/JPSJ.75.044711\r\nCeRhGe3,I4mm,4mm,BaNiSn3-type,,Yes,Yes,PM,10.1143/JPSJ.77.064716\r\nCeRuSi3,I4mm,4mm,BaNiSn3-type,,,,PM,10.1143/JPSJ.77.064716\r\nLaIrGe3,I4mm,4mm,BaNiSn3-type,,,,PM,10.1143/JPSJ.77.064717\r\nLaFeGe3,I4mm,4mm,BaNiSn3-type,,,,PM,10.1143/JPSJ.77.064717\r\nPrCoGe3,I4mm,4mm,BaNiSn3-type,,,,PM,10.1143/JPSJ.77.064717\r\nCaIrSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1016/j.physc.2009.10.120\r\nCaPtSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1134/S0021364010170157\r\nSrAuSi3,I4mm,4mm,BaNiSn3-type,,Yes,,PM,10.1021/cm500032u\r\nEuPdGe3,I4mm,4mm,BaNiSn3-type,,,Yes,PM,10.1016/j.ssc.2012.02.022\r\nEuPtSi3,I4mm,4mm,anti-perovskite,,,Yes,PM,10.1103/PhysRevB.81.144414\r\nNdPdIn2,I4mm,4mm,HfNiGa2-Type,,,,PM,10.1021/cm031139m\r\nSmPdIn2,I4mm,4mm,HfNiGa2-Type,,,,PM,10.1021/cm031139m\r\nGdPdIn2,I4mm,4mm,HfNiGa2-Type,,,,PM,10.1021/cm031139m\r\nErPdIn2,I4mm,4mm,HfNiGa2-Type,,,,PM,10.1021/cm031139m\r\nTmPdIn2,I4mm,4mm,HfNiGa2-Type,,,,PM,10.1021/cm031139m\r\nLuPdIn2,I4mm,4mm,HfNiGa2-Type,,,,PM,10.1021/cm031139m\r\nLa2NiAl7,I4mm,4mm,BaAl4-type,,,,PM,10.1021/cm050513a\r\nGeP,I4mm,4mm,rock salt,,Yes,,PM,10.1016/0022-4596(70)90005-8\r\nIr9Al28,P3_1c,3m,Ir9Al28-type,,,,PM,10.1016/j.jallcom.2005.06.027\r\nγ-Bi2Pt,P3_1m,3m,γ-Bi2Pt,,,,PM,10.1002/zaac.201400331\r\nAu6.05Zn12.51,P3_1m,3m,γ-brass,,,,PM,10.1021/ic301933a\r\nBa21Al40,P3_1m,3m,kagome-derived,,,,PM,10.1021/ic0400235\r\nLi17Ag3Sn6,P3_1m,3m,kagome-derived,,,,PM,10.1021/ja038868n\r\nCr5Al8,R3m,3m,γ-brass,,,,PM,10.1107/S0567740874004997\r\nMn5Al8,R3m,3m,Cr5Al8-type,Yes,,,DPM,10.1007/BF02672582\r\nCu7.8Al5,R3m,3m,γ-brass,,,,PM,10.1107/S0108768191005694\r\nCu7Hg6,R3m,3m,γ-brass,,,,PM,10.3891/acta.chem.scand.23-1181\r\nNbS2,R3m,3m,NbS2-type,,Yes,,PM,10.1107/S0567740874003220\r\nPr2Fe17,R3m,3m,Th2Zn17-type,,,Yes,PM,10.1103/PhysRevB.68.054424\r\nPr2Co17,R3m,3m,Th2Zn17-type,,,,PM,10.1103/PhysRevB.68.054424\r\nSn4As3,R3m,3m,Sn4As3-type,,Yes,,PM,10.1002/zaac.19683630102\r\nSn4P3,R3m,3m,Sn4As3-type,,Yes,,PM,10.1002/zaac.19683630102\r\nLa4Mg5Ge6,Cmc2_1,mm2,Zintl,,,,PM,10.1021/ic2014732\r\nLa4Mg7Ge6,Cmc2_1,mm2,Zintl,,,,PM,10.1021/ic2014732\r\nYb2Ga4Ge6,Cmc2_1,mm2,Zintl,,,,PM,10.1002/chem.200305755\r\n\"Ce2Rh3(Pb,Bi)5\",Cmc2_1,mm2,Y2Rh3Sn5-type,,,Yes,PM,10.1016/j.jssc.2007.06.012\r\nEu2Pt3Sn5,Cmc2_1,mm2,Y2Rh3Sn5-type,,,Yes,PM,10.1524/zkri.2009.1160\r\nLu4Zn5Ge6,Cmc2_1,mm2,Lu4Zn5Ge6-type,,,,PM,10.1016/j.intermet.2013.02.018\r\nHg3Te2Br2,R3,3,defect antiperovskite,Yes,,,PM,10.1038/s41467-021-21836-7\r\nIn2S3,R3m,3m,\"2D, alpha-In2Se3\",P,,,APM,10.1039/D1MH01556G\r\nIn2Se3,R3m,3m,\"2D, alpha-In2Se3\",P,,,APM,10.1039/D1MH01556G\r\nIn2Te3,R3m,3m,\"2D, alpha-In2Se3\",P,,,APM,10.1039/D1MH01556G\r\nNaYMnReO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nNaYFeReO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nNaYCoReO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nNaYNiReO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nNaYMnOsO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nNaYCoOsO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nNaYNiOsO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nNaYFeWO3,P2_1,2,double perovskite,P,,Yes,PM,10.1021/acs.chemmater.0c02976\r\nYAl2,P6mm,6mm,2D,P,,,APM,10.1021/acs.jpclett.0c03136\r\nCaRh2,P6mm,6mm,2D,P,,,APM,10.1021/acs.jpclett.0c03136\r\ndoped SiGe,P3m1,3m,\"2D, PbTe-type\",P,,,APM,10.1088/1361-648X/abdce9/pdf\r\ndoped SiSn,P3m1,3m,\"2D, PbTe-type\",P,,,APM,10.1088/1361-648X/abdce9/pdf\r\ndoped GeSn,P3m1,3m,\"2D, PbTe-type\",P,,,APM,10.1088/1361-648X/abdce9/pdf\r\nKNbO3/BaTiO3,P4mm,4mm,perovskite,P,,Yes,APM,10.1016/j.commatsci.2020.110235\r\n(SrRuO3)1/(BaTiO3)10,mm2*,mm2,perovskite,,,Yes,APM,10.1021/acs.nanolett.0c03417\r\nstrained EuTiO3−xHx,Pmm2,mm2,perovskite,P,,Yes,EPM,10.1103/PhysRevB.102.224102\r\nKTiO2H,unknown,unknown,perovskite,P,Yes,,DDF,10.1103/PhysRevMaterials.5.054802\r\nRbTiO2H,unknown,unknown,perovskite,P,Yes,,DDF,10.1103/PhysRevMaterials.5.054802\r\nCsTiO2H,unknown,unknown,perovskite,P,Yes,,DDF,10.1103/PhysRevMaterials.5.054802\r\ndoped PbZrO3,unknown,unknown,perovskite,P,,,DDF,10.1103/PhysRevB.102.134118\r\nLaFeAsO1-xHx,mm2*,mm2,LaFeAsO1-xHx-type,,Yes,Yes,PM,10.21203/rs.3.rs-77544/v1\r\nPb2CoOsO6,Pc,m,double perovskite,P,,Yes,DPM,10.1103/PhysRevB.102.144418\r\nPrAlGe,I4_1md,4mm,PrAlGe-type,,,Yes,PM,10.1038/s41467-020-16879-1\r\nPbTe monolayer (doped),P3m1,3m,\"2D, PbTe-type\",P,,,\"EPM, APM\",10.1039/d0nh00188k\r\nen-CoS,Pca2_1,mm2,Intercalated TTMC,,,Yes,PM,10.1021/acs.chemmater.1c00540\r\nEu(Ti0.875Nb0.125)3,P4mm,4mm,perovskite,P,Yes,Yes,EPM,10.48550/arXiv.2203.10646\r\nBi5Mn5O17,Pmn2_1/Pm2_1n,mm2,layered perovskite,P,Yes,Yes,APM,10.1038/s41467-020-18664-6\r\n2D In,3m*,3m,2-D polar metal heterostructures,,,,PM,10.1021/acsnano.1c05944\r\n2D Ga,3m*,3m,2-D polar metal heterostructures,,,,PM,10.1021/acsnano.1c05944\r\n2D In/Ga,3m*,3m,2-D polar metal heterostructures,,,,PM,10.1021/acsnano.1c05944\r\n(Fe0.5Co0.5)5GeTe2,P6_3mc,6mm,wurtzite,,,Yes,PM,10.1126/sciadv.abm7103\r\nGdCaMnNiO6,P2_1,2,double perovskite,P,Yes,,PM,10.2139/ssrn.4147202\r\nLaCaMnNiO6,P2_1,2,double perovskite,P,Yes,,PM,10.2139/ssrn.4147202\r\nSmCaMnNiO6,P2_1,2,double perovskite,P,Yes,,PM,10.2139/ssrn.4147202\r\nTmCaMnNiO6,P2_1,2,double perovskite,P,Yes,,PM,10.2139/ssrn.4147202\r\nSrTiO3-based 2DEGs,unknown,unknown,perovskite,Yes,Yes,Yes,\"IPM, APM, DPM\",\"10.1002/adma.201200667\n10.1103/PhysRevMaterials.4.041002\n10.1038/s41586-020-2197-9\"\r\nDoped GeTe,R3m,3m,halite,Yes,Yes,Yes,\"DPM, APM\",\"10.1038/ncomms15033\n10.1103/PhysRevLett.112.047202\"\r\nLaAlO3/EuTiO3/Ca:SrTiO3,unknown,unknown,perovskite,Yes,,yes,\"IPM, APM, MEMF\",10.1038/s41567-023-01983-y\r\n"
  },
  {
    "path": "dataset/Polar Metals Materials Database/mtd_data.json",
    "content": "[{\"Material\": \"BaTiO3 (La-doped)\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"Yes\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"DDF\", \"Reference (DOI)\": \"10.1038/s41598-017-04635-3\"}, {\"Material\": \"BaTiO3-d\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"Yes\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"DDF\", \"Reference (DOI)\": \"10.1103/PhysRevLett.104.147602\"}, {\"Material\": \"PbTiO3-d\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.94.224107\"}, {\"Material\": \"PbTi(1-x)NbxO3\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.96.165206\"}, {\"Material\": \"BiFeO3-d\", \"SG\": \"R3c\", \"PG\": \"3m\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.93.174110\"}, {\"Material\": \"Sr(1-x)CaxTiO3-d\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"Yes\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"DPM\", \"Reference (DOI)\": \"10.1038/NPHYS4085\"}, {\"Material\": \"BaMnO3 (n-doped)\", \"SG\": \"Amm2\", \"PG\": \"mm2\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.97.054107\"}, {\"Material\": \"BiAlO3 (n-doped)\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.97.054107\"}, {\"Material\": \"BaTiO3/SrTiO3/LaTiO3\", \"SG\": \"mm4*\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"IPM\", \"Reference (DOI)\": \"10.1038/s41467-018-03964-9\"}, {\"Material\": \"LaAlO3/Ba0.2Sr0.8TiO3/SrTiO3\", \"SG\": \"unknown\", \"PG\": \"unknown\", \"Structure-Type\": \"perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"IPM\", \"Reference (DOI)\": \"10.1038/s42005-019-0227-4\"}, {\"Material\": \"LaFeO3/YFeO3 (n-doped)\", \"SG\": \"Pmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"IPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.97.054107\"}, {\"Material\": \"NdNiO3 on (111) LaAlO3\", \"SG\": \"Pc\", \"PG\": \"m\", \"Structure-Type\": \"perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1038/nature17628\"}, {\"Material\": \"LaNiO3 on (111) LaAlO3\", \"SG\": \"Pc\", \"PG\": \"m\", \"Structure-Type\": \"perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1038/nature17628\"}, {\"Material\": \"LiOsO3\", \"SG\": \"R3c\", \"PG\": \"3m\", \"Structure-Type\": \"LiNbO3-type\", \"Tc\": \"Yes\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"DPM\", \"Reference (DOI)\": \"10.1038/NMAT3754\"}, {\"Material\": \"LiNbO3 (n-doped)\", \"SG\": \"R3c\", \"PG\": \"3m\", \"Structure-Type\": \"LiNbO3-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"DDF\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.3.054405\"}, {\"Material\": \"MgReO3\", \"SG\": \"R3c\", \"PG\": \"3m\", \"Structure-Type\": \"LiNbO3-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.90.094108\"}, {\"Material\": \"TiGaO3\", \"SG\": \"R3c\", \"PG\": \"3m\", \"Structure-Type\": \"LiNbO3-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.90.094108\"}, {\"Material\": \"Ca3Ru2O7\", \"SG\": \"Bb2_1m\", \"PG\": \"mm2\", \"Structure-Type\": \"Ruddlesden-Popper\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.nanolett.8b00633\"}, {\"Material\": \"(Sr,Ca)Ru2O6\", \"SG\": \"Pmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/0953-8984/26/26/265501\"}, {\"Material\": \"Bi5Ti5O17\", \"SG\": \"Pm2_1n\", \"PG\": \"mm2\", \"Structure-Type\": \"layered perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1038/ncomms11211\"}, {\"Material\": \"BiPbTi2O6\", \"SG\": \"Pmm2\", \"PG\": \"mm2\", \"Structure-Type\": \"post-perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1038/s43246-019-0005-6\"}, {\"Material\": \"La2Ti2O7 (n-doped)\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"layered perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.97.054107\"}, {\"Material\": \"Sr2Nb2O7 (n-doped)\", \"SG\": \"Cmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"layered perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.97.054107\"}, {\"Material\": \"MgCNi3\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.2.125004\"}, {\"Material\": \"ZnCNi3\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.2.125004\"}, {\"Material\": \"CdCNi3\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.2.125004\"}, {\"Material\": \"CeSiPt3\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"antiperovskite\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.92.027003\"}, {\"Material\": \"LiGaGe\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.99.195154\"}, {\"Material\": \"SrHgPb\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.121.106404\"}, {\"Material\": \"SrHgSn\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.121.106404\"}, {\"Material\": \"CaHgSn\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.121.106404\"}, {\"Material\": \"KMgSb0.2Bi0.8\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.117.076401\"}, {\"Material\": \"CaAgBi\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.1.044201\"}, {\"Material\": \"LiZnBi\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.96.115203\"}, {\"Material\": \"LaAuGe\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1063/1.5132339\"}, {\"Material\": \"LaPtSb\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"LiGaGe-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1063/1.5132339\"}, {\"Material\": \"WTe2\", \"SG\": \"Pnm2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"2D\", \"Tc\": \"Yes\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1038/s41586-018-0336-3\"}, {\"Material\": \"MoTe2\", \"SG\": \"Pnm2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"2D\", \"Tc\": \"Yes\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1126/sciadv.1601378\"}, {\"Material\": \"CrN\", \"SG\": \"6mm*\", \"PG\": \"6mm\", \"Structure-Type\": \"2D\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1103/PhysRevB.96.235415\"}, {\"Material\": \"CrB2\", \"SG\": \"6mm*\", \"PG\": \"6mm\", \"Structure-Type\": \"2D\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1103/PhysRevB.96.235415\"}, {\"Material\": \"FeB2\", \"SG\": \"6mm*\", \"PG\": \"6mm\", \"Structure-Type\": \"2D\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1021/acs.nanolett.6b02335\"}, {\"Material\": \"P\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"\\u03b1-La-like\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/1361-648X/aadeaa\"}, {\"Material\": \"As\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"\\u03b1-La-like\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/1361-648X/aadeaa\"}, {\"Material\": \"Sb\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"\\u03b1-La-like\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/1361-648X/aadeaa\"}, {\"Material\": \"Bi\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"\\u03b1-La-like\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/1361-648X/aadeaa\"}, {\"Material\": \"SnP\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"rock salt\", \"Tc\": \"Yes\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"DPM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.119.207001\"}, {\"Material\": \"PdBi\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"PdBi-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.phpro.2013.04.062\"}, {\"Material\": \"UIr\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"PdBi-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1007/978-3-642-24624-1_2\"}, {\"Material\": \"LaNiC2\", \"SG\": \"Amm2\", \"PG\": \"mm2\", \"Structure-Type\": \"CeNiC2-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.physc.2014.01.008\"}, {\"Material\": \"NdRhC2\", \"SG\": \"Amm2\", \"PG\": \"mm2\", \"Structure-Type\": \"CeNiC2-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00006a007\"}, {\"Material\": \"PrRhC2\", \"SG\": \"Amm2\", \"PG\": \"mm2\", \"Structure-Type\": \"CeNiC2-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00006a007\"}, {\"Material\": \"LaSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"CeSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"PrSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"NdSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"PmSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"SmSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"EuSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"GdSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"TbSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"DySr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"HoSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"ErSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"TmSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"YbSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"YSr2Cu2GaO7\", \"SG\": \"Ima2\", \"PG\": \"mm2\", \"Structure-Type\": \"LnSr2Cu2GaO7\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm00017a032\"}, {\"Material\": \"V2Hf\", \"SG\": \"Imm2\", \"PG\": \"mm2\", \"Structure-Type\": \"Laves phase\", \"Tc\": \"Yes\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"DPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.17.1136\"}, {\"Material\": \"Li2IrSi3\", \"SG\": \"P3_1c\", \"PG\": \"3m\", \"Structure-Type\": \"kagome\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.7566/JPSJ.83.093706\"}, {\"Material\": \"Mg2Al3\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"Samson phase\", \"Tc\": \"Yes\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"DPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.76.014528\"}, {\"Material\": \"La5B2C6\", \"SG\": \"P4\", \"PG\": \"4\", \"Structure-Type\": \"La5B2C6-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/0022-5088(83)90520-9\"}, {\"Material\": \"BaPtSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.80.064504\"}, {\"Material\": \"CeIrSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJS.77SA.37\"}, {\"Material\": \"CeRhSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.76.051010\"}, {\"Material\": \"LaPtSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.89.094509\"}, {\"Material\": \"LaPdSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.89.094509\"}, {\"Material\": \"CeIrGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.jmmm.2006.10.151\"}, {\"Material\": \"EuNiGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.87.064406\"}, {\"Material\": \"LaRhGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1063/5.0042924\"}, {\"Material\": \"IrRhGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1063/5.0042924\"}, {\"Material\": \"PdRhGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1063/5.0042924\"}, {\"Material\": \"SrPdGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/1742-6596/273/1/012078\"}, {\"Material\": \"SrPtGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/1742-6596/273/1/012078\"}, {\"Material\": \"PrPdIn2\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"HfNiGa2-Type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm031139m\"}, {\"Material\": \"CePt3Si\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"anti-perovskite\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.92.027003\"}, {\"Material\": \"Li2(Pd1-xPtx)3B\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"Li2(Pd1-xPtx)3B\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/1742-6596/400/2/022096\"}, {\"Material\": \"KCu7P3\", \"SG\": \"P31m\", \"PG\": \"3m\", \"Structure-Type\": \"2D\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.inorgchem.9b01336\"}, {\"Material\": \"Bi2FeCrO6\", \"SG\": \"R3\", \"PG\": \"3\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevLett.123.107201\"}, {\"Material\": \"CeAuGe\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"AlB2-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/0304-8853(95)00430-0\"}, {\"Material\": \"LuAuGe\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"AlB2-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/0925-8388(95)02069-1\"}, {\"Material\": \"ScAuGe\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"AlB2-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/0925-8388(95)02069-1\"}, {\"Material\": \"HoAuGe\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"NdPtSb-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1088/0953-8984/13/11/315\"}, {\"Material\": \"CeCuSn\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"AlB2-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.jallcom.2004.09.086\"}, {\"Material\": \"La15Ge9C\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"La15Ge9Fe-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.jallcom.2011.03.092\"}, {\"Material\": \"La15Ge9Fe\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"Mn5Si3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ic9515158\"}, {\"Material\": \"La15Ge9Co\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"Mn5Si3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ic9515158\"}, {\"Material\": \"La15Ge9Ni\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"Mn5Si3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ic9515158\"}, {\"Material\": \"Sr3Cu8Sn4\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"BaAl4-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.intermet.2011.02.018\"}, {\"Material\": \"IrMg2.03In.97\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"FeGa3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.intermet.2003.12.001\"}, {\"Material\": \"IrMg2.20In.80\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"FeGa3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.intermet.2003.12.001\"}, {\"Material\": \"CaAlSi\", \"SG\": \"P6_3\", \"PG\": \"6\", \"Structure-Type\": \"MgB2-Type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.75.043713\"}, {\"Material\": \"TlV6S8\", \"SG\": \"P6_3\", \"PG\": \"6\", \"Structure-Type\": \"Nb3Te4-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/S0038-1098(01)00333-7\"}, {\"Material\": \"KV6S8\", \"SG\": \"P6_3\", \"PG\": \"6\", \"Structure-Type\": \"Nb3Te4-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/S0038-1098(01)00333-7\"}, {\"Material\": \"RbV6S8\", \"SG\": \"P6_3\", \"PG\": \"6\", \"Structure-Type\": \"Nb3Te4-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/S0038-1098(01)00333-7\"}, {\"Material\": \"CsV6S8\", \"SG\": \"P6_3\", \"PG\": \"6\", \"Structure-Type\": \"Nb3Te4-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/S0038-1098(01)00333-7\"}, {\"Material\": \"LaPt3B\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"anti-perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/S0925-8388(03)00373-6\"}, {\"Material\": \"PrPt3B\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"anti-perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/S0925-8388(03)00373-6\"}, {\"Material\": \"NdPt3B\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"anti-perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/S0925-8388(03)00373-6\"}, {\"Material\": \"LaRhSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/0025-5408(84)90017-5\"}, {\"Material\": \"LaIrSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/0025-5408(84)90017-5\"}, {\"Material\": \"CeCoGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.jmmm.2006.10.717\"}, {\"Material\": \"LaCoGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.75.044711\"}, {\"Material\": \"CeRhGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.77.064716\"}, {\"Material\": \"CeRuSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.77.064716\"}, {\"Material\": \"LaIrGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.77.064717\"}, {\"Material\": \"LaFeGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.77.064717\"}, {\"Material\": \"PrCoGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1143/JPSJ.77.064717\"}, {\"Material\": \"CaIrSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.physc.2009.10.120\"}, {\"Material\": \"CaPtSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1134/S0021364010170157\"}, {\"Material\": \"SrAuSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm500032u\"}, {\"Material\": \"EuPdGe3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaNiSn3-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.ssc.2012.02.022\"}, {\"Material\": \"EuPtSi3\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"anti-perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.81.144414\"}, {\"Material\": \"NdPdIn2\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"HfNiGa2-Type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm031139m\"}, {\"Material\": \"SmPdIn2\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"HfNiGa2-Type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm031139m\"}, {\"Material\": \"GdPdIn2\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"HfNiGa2-Type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm031139m\"}, {\"Material\": \"ErPdIn2\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"HfNiGa2-Type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm031139m\"}, {\"Material\": \"TmPdIn2\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"HfNiGa2-Type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm031139m\"}, {\"Material\": \"LuPdIn2\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"HfNiGa2-Type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm031139m\"}, {\"Material\": \"La2NiAl7\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"BaAl4-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/cm050513a\"}, {\"Material\": \"GeP\", \"SG\": \"I4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"rock salt\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/0022-4596(70)90005-8\"}, {\"Material\": \"Ir9Al28\", \"SG\": \"P3_1c\", \"PG\": \"3m\", \"Structure-Type\": \"Ir9Al28-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.jallcom.2005.06.027\"}, {\"Material\": \"\\u03b3-Bi2Pt\", \"SG\": \"P3_1m\", \"PG\": \"3m\", \"Structure-Type\": \"\\u03b3-Bi2Pt\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1002/zaac.201400331\"}, {\"Material\": \"Au6.05Zn12.51\", \"SG\": \"P3_1m\", \"PG\": \"3m\", \"Structure-Type\": \"\\u03b3-brass\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ic301933a\"}, {\"Material\": \"Ba21Al40\", \"SG\": \"P3_1m\", \"PG\": \"3m\", \"Structure-Type\": \"kagome-derived\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ic0400235\"}, {\"Material\": \"Li17Ag3Sn6\", \"SG\": \"P3_1m\", \"PG\": \"3m\", \"Structure-Type\": \"kagome-derived\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ja038868n\"}, {\"Material\": \"Cr5Al8\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"\\u03b3-brass\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1107/S0567740874004997\"}, {\"Material\": \"Mn5Al8\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"Cr5Al8-type\", \"Tc\": \"Yes\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"DPM\", \"Reference (DOI)\": \"10.1007/BF02672582\"}, {\"Material\": \"Cu7.8Al5\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"\\u03b3-brass\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1107/S0108768191005694\"}, {\"Material\": \"Cu7Hg6\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"\\u03b3-brass\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.3891/acta.chem.scand.23-1181\"}, {\"Material\": \"NbS2\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"NbS2-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1107/S0567740874003220\"}, {\"Material\": \"Pr2Fe17\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"Th2Zn17-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.68.054424\"}, {\"Material\": \"Pr2Co17\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"Th2Zn17-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1103/PhysRevB.68.054424\"}, {\"Material\": \"Sn4As3\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"Sn4As3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1002/zaac.19683630102\"}, {\"Material\": \"Sn4P3\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"Sn4As3-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1002/zaac.19683630102\"}, {\"Material\": \"La4Mg5Ge6\", \"SG\": \"Cmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"Zintl\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ic2014732\"}, {\"Material\": \"La4Mg7Ge6\", \"SG\": \"Cmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"Zintl\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/ic2014732\"}, {\"Material\": \"Yb2Ga4Ge6\", \"SG\": \"Cmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"Zintl\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1002/chem.200305755\"}, {\"Material\": \"Ce2Rh3(Pb,Bi)5\", \"SG\": \"Cmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"Y2Rh3Sn5-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.jssc.2007.06.012\"}, {\"Material\": \"Eu2Pt3Sn5\", \"SG\": \"Cmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"Y2Rh3Sn5-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1524/zkri.2009.1160\"}, {\"Material\": \"Lu4Zn5Ge6\", \"SG\": \"Cmc2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"Lu4Zn5Ge6-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1016/j.intermet.2013.02.018\"}, {\"Material\": \"Hg3Te2Br2\", \"SG\": \"R3\", \"PG\": \"3\", \"Structure-Type\": \"defect antiperovskite\", \"Tc\": \"Yes\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1038/s41467-021-21836-7\"}, {\"Material\": \"In2S3\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"2D, alpha-In2Se3\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1039/D1MH01556G\"}, {\"Material\": \"In2Se3\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"2D, alpha-In2Se3\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1039/D1MH01556G\"}, {\"Material\": \"In2Te3\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"2D, alpha-In2Se3\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1039/D1MH01556G\"}, {\"Material\": \"NaYMnReO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"NaYFeReO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"NaYCoReO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"NaYNiReO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"NaYMnOsO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"NaYCoOsO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"NaYNiOsO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"NaYFeWO3\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.0c02976\"}, {\"Material\": \"YAl2\", \"SG\": \"P6mm\", \"PG\": \"6mm\", \"Structure-Type\": \"2D\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1021/acs.jpclett.0c03136\"}, {\"Material\": \"CaRh2\", \"SG\": \"P6mm\", \"PG\": \"6mm\", \"Structure-Type\": \"2D\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1021/acs.jpclett.0c03136\"}, {\"Material\": \"doped SiGe\", \"SG\": \"P3m1\", \"PG\": \"3m\", \"Structure-Type\": \"2D, PbTe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1088/1361-648X/abdce9/pdf\"}, {\"Material\": \"doped SiSn\", \"SG\": \"P3m1\", \"PG\": \"3m\", \"Structure-Type\": \"2D, PbTe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1088/1361-648X/abdce9/pdf\"}, {\"Material\": \"doped GeSn\", \"SG\": \"P3m1\", \"PG\": \"3m\", \"Structure-Type\": \"2D, PbTe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1088/1361-648X/abdce9/pdf\"}, {\"Material\": \"KNbO3/BaTiO3\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1016/j.commatsci.2020.110235\"}, {\"Material\": \"(SrRuO3)1/(BaTiO3)10\", \"SG\": \"mm2*\", \"PG\": \"mm2\", \"Structure-Type\": \"perovskite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1021/acs.nanolett.0c03417\"}, {\"Material\": \"strained\\u00a0EuTiO3\\u2212xHx\", \"SG\": \"Pmm2\", \"PG\": \"mm2\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.102.224102\"}, {\"Material\": \"KTiO2H\", \"SG\": \"unknown\", \"PG\": \"unknown\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"DDF\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.5.054802\"}, {\"Material\": \"RbTiO2H\", \"SG\": \"unknown\", \"PG\": \"unknown\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"DDF\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.5.054802\"}, {\"Material\": \"CsTiO2H\", \"SG\": \"unknown\", \"PG\": \"unknown\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"DDF\", \"Reference (DOI)\": \"10.1103/PhysRevMaterials.5.054802\"}, {\"Material\": \"doped PbZrO3\", \"SG\": \"unknown\", \"PG\": \"unknown\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"DDF\", \"Reference (DOI)\": \"10.1103/PhysRevB.102.134118\"}, {\"Material\": \"LaFeAsO1-xHx\", \"SG\": \"mm2*\", \"PG\": \"mm2\", \"Structure-Type\": \"LaFeAsO1-xHx-type\", \"Tc\": \"\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.21203/rs.3.rs-77544/v1\"}, {\"Material\": \"Pb2CoOsO6\", \"SG\": \"Pc\", \"PG\": \"m\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"DPM\", \"Reference (DOI)\": \"10.1103/PhysRevB.102.144418\"}, {\"Material\": \"PrAlGe\", \"SG\": \"I4_1md\", \"PG\": \"4mm\", \"Structure-Type\": \"PrAlGe-type\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1038/s41467-020-16879-1\"}, {\"Material\": \"PbTe monolayer (doped)\", \"SG\": \"P3m1\", \"PG\": \"3m\", \"Structure-Type\": \"2D, PbTe-type\", \"Tc\": \"P\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"EPM, APM\", \"Reference (DOI)\": \"10.1039/d0nh00188k\"}, {\"Material\": \"en-CoS\", \"SG\": \"Pca2_1\", \"PG\": \"mm2\", \"Structure-Type\": \"Intercalated TTMC\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acs.chemmater.1c00540\"}, {\"Material\": \"Eu(Ti0.875Nb0.125)3\", \"SG\": \"P4mm\", \"PG\": \"4mm\", \"Structure-Type\": \"perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"EPM\", \"Reference (DOI)\": \"10.48550/arXiv.2203.10646\"}, {\"Material\": \"Bi5Mn5O17\", \"SG\": \"Pmn2_1/Pm2_1n\", \"PG\": \"mm2\", \"Structure-Type\": \"layered perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"APM\", \"Reference (DOI)\": \"10.1038/s41467-020-18664-6\"}, {\"Material\": \"2D In\", \"SG\": \"3m*\", \"PG\": \"3m\", \"Structure-Type\": \"2-D polar metal heterostructures\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acsnano.1c05944\"}, {\"Material\": \"2D Ga\", \"SG\": \"3m*\", \"PG\": \"3m\", \"Structure-Type\": \"2-D polar metal heterostructures\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acsnano.1c05944\"}, {\"Material\": \"2D In/Ga\", \"SG\": \"3m*\", \"PG\": \"3m\", \"Structure-Type\": \"2-D polar metal heterostructures\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1021/acsnano.1c05944\"}, {\"Material\": \"(Fe0.5Co0.5)5GeTe2\", \"SG\": \"P6_3mc\", \"PG\": \"6mm\", \"Structure-Type\": \"wurtzite\", \"Tc\": \"\", \"Tsc\": \"\", \"TM\": \"Yes\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.1126/sciadv.abm7103\"}, {\"Material\": \"GdCaMnNiO6\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.2139/ssrn.4147202\"}, {\"Material\": \"LaCaMnNiO6\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.2139/ssrn.4147202\"}, {\"Material\": \"SmCaMnNiO6\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.2139/ssrn.4147202\"}, {\"Material\": \"TmCaMnNiO6\", \"SG\": \"P2_1\", \"PG\": \"2\", \"Structure-Type\": \"double perovskite\", \"Tc\": \"P\", \"Tsc\": \"Yes\", \"TM\": \"\", \"Subclass\": \"PM\", \"Reference (DOI)\": \"10.2139/ssrn.4147202\"}, {\"Material\": \"SrTiO3-based 2DEGs\", \"SG\": \"unknown\", \"PG\": \"unknown\", \"Structure-Type\": \"perovskite\", \"Tc\": \"Yes\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"IPM, APM, DPM\", \"Reference (DOI)\": \"10.1002/adma.201200667\\n10.1103/PhysRevMaterials.4.041002\\n10.1038/s41586-020-2197-9\"}, {\"Material\": \"Doped GeTe\", \"SG\": \"R3m\", \"PG\": \"3m\", \"Structure-Type\": \"halite\", \"Tc\": \"Yes\", \"Tsc\": \"Yes\", \"TM\": \"Yes\", \"Subclass\": \"DPM, APM\", \"Reference (DOI)\": \"10.1038/ncomms15033\\n10.1103/PhysRevLett.112.047202\"}, {\"Material\": \"LaAlO3/EuTiO3/Ca:SrTiO3\", \"SG\": \"unknown\", \"PG\": \"unknown\", \"Structure-Type\": \"perovskite\", \"Tc\": \"Yes\", \"Tsc\": \"\", \"TM\": \"yes\", \"Subclass\": \"IPM, APM, MEMF\", \"Reference (DOI)\": \"10.1038/s41567-023-01983-y\"}]"
  },
  {
    "path": "dataset/chembl/chembl.csv",
    "content": "smiles,inchi,selfies,iupac,lipophilicity\nCn1c(CN2CCN(CC2)c3ccc(Cl)cc3)nc4ccccc14,\"InChI=1S/C19H21ClN4/c1-22-18-5-3-2-4-17(18)21-19(22)14-23-10-12-24(13-11-23)16-8-6-15(20)7-9-16/h2-9H,10-14H2,1H3\",[C][N][C][Branch2][Ring1][#Branch1][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][C][=C][C][=C][C][=C][Ring2][Ring1][#Branch1][Ring1][=Branch1],2-[[4-(4-chlorophenyl)piperazin-1-yl]methyl]-1-methylbenzimidazole,3.54\nCOC(=O)[C@@H](N1CCc2sccc2C1)c3ccccc3Cl,\"InChI=1S/C16H16ClNO2S/c1-20-16(19)15(12-4-2-3-5-13(12)17)18-8-6-14-11(10-18)7-9-21-14/h2-5,7,9,15H,6,8,10H2,1H3/t15-/m0/s1\",[C][O][C][=Branch1][C][=O][C@@H1][Branch1][=C][N][C][C][C][S][C][=C][C][=Ring1][Branch1][C][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],\"methyl (2s)-2-(2-chlorophenyl)-2-(6,7-dihydro-4h-thieno[3,2-c]pyridin-5-yl)acetate\",3.69\nOC[C@H](O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C19H18ClN3O4S/c20-16-7-11-6-13(22-18(11)28-16)17(26)21-14-5-10-3-1-2-4-15(10)23(19(14)27)8-12(25)9-24/h1-4,6-7,12,14,22,24-25H,5,8-9H2,(H,21,26)/t12-,14?/m1/s1\",[O][C][C@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-[(2r)-2,3-dihydroxypropyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.37\nCOc1ccc(cc1)C2=COc3cc(OC)cc(OC)c3C2=O,\"InChI=1S/C18H16O5/c1-20-12-6-4-11(5-7-12)14-10-23-16-9-13(21-2)8-15(22-3)17(16)18(14)19/h4-10H,1-3H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][Ring1][O][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][C][Ring1][=C][=O],\"5,7-dimethoxy-3-(4-methoxyphenyl)chromen-4-one\",3.05\nO=C1CCCCCN1,\"InChI=1S/C6H11NO/c8-6-4-2-1-3-5-7-6/h1-5H2,(H,7,8)\",[O][=C][C][C][C][C][C][N][Ring1][#Branch1],azepan-2-one,-0.08\nNc1ccc(cc1)c2nc3ccc(O)cc3s2,\"InChI=1S/C13H10N2OS/c14-9-3-1-8(2-4-9)13-15-11-6-5-10(16)7-12(11)17-13/h1-7,16H,14H2\",[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][S][Ring1][#Branch2],\"2-(4-aminophenyl)-1,3-benzothiazol-6-ol\",3.2\nCCC(COC(=O)c1cc(OC)c(OC)c(OC)c1)(N(C)C)c2ccccc2,\"InChI=1S/C22H29NO5/c1-7-22(23(2)3,17-11-9-8-10-12-17)15-28-21(24)16-13-18(25-4)20(27-6)19(14-16)26-5/h8-14H,7,15H2,1-6H3\",[C][C][C][Branch2][Ring1][O][C][O][C][=Branch1][C][=O][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][N][Branch1][=Branch1][N][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(2-dimethylamino-2-phenylbutyl) 3,4,5-trimethoxybenzoate\",3.77\nCOc1cc(ccc1N2CC[C@@H](O)C2)N3N=Nc4cc(sc4C3=O)c5ccc(Cl)cc5,\"InChI=1S/C22H19ClN4O3S/c1-30-19-10-15(6-7-18(19)26-9-8-16(28)12-26)27-22(29)21-17(24-25-27)11-20(31-21)13-2-4-14(23)5-3-13/h2-7,10-11,16,28H,8-9,12H2,1H3/t16-/m1/s1\",[C][O][C][=C][C][=Branch1][S][=C][C][=C][Ring1][=Branch1][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1][N][N][=N][C][C][=C][Branch1][=Branch2][S][C][=Ring1][Branch1][C][Ring1][=Branch2][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"6-(4-chlorophenyl)-3-[4-[(3r)-3-hydroxypyrrolidin-1-yl]-3-methoxyphenyl]thieno[2,3-e]triazin-4-one\",3.15\nCNCC[C@@H](Oc1ccccc1C)c2ccccc2,\"InChI=1S/C17H21NO/c1-14-8-6-7-11-16(14)19-17(12-13-18-2)15-9-4-3-5-10-15/h3-11,17-18H,12-13H2,1-2H3/t17-/m1/s1\",[C][N][C][C][C@@H1][Branch1][O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],(3r)-n-methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine,1.2\nCOc1cnc(nc1N(C)C)c2ccccn2,\"InChI=1S/C12H14N4O/c1-16(2)12-10(17-3)8-14-11(15-12)9-6-4-5-7-13-9/h4-8H,1-3H3\",[C][O][C][=C][N][=C][Branch1][#Branch2][N][=C][Ring1][=Branch1][N][Branch1][C][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1],\"5-methoxy-n,n-dimethyl-2-pyridin-2-ylpyrimidin-4-amine\",1.9\nCC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C,\"InChI=1S/C21H30O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12,16-19H,4-11H2,1-3H3/t16-,17+,18-,19-,20-,21+/m0/s1\",[C][C][=Branch1][C][=O][C@H1][C][C][C@H1][C@@H1][C][C][C][=C][C][=Branch1][C][=O][C][C][C@][Ring1][#Branch1][Branch1][C][C][C@H1][Ring1][N][C][C][C@][Ring2][Ring1][Ring1][Ring1][S][C],\"(8s,9s,10r,13s,14s,17s)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one\",3.94\nCN(C)c1ccnc2sc(C(=O)NCc3ccccc3)c(N)c12,\"InChI=1S/C17H18N4OS/c1-21(2)12-8-9-19-17-13(12)14(18)15(23-17)16(22)20-10-11-6-4-3-5-7-11/h3-9H,10,18H2,1-2H3,(H,20,22)\",[C][N][Branch1][C][C][C][=C][C][=N][C][S][C][Branch1][#C][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][C][N][C][Ring2][Ring1][Ring2][=Ring1][S],\"3-amino-4-dimethylamino-n-(phenylmethyl)thieno[5,4-b]pyridine-2-carboxamide\",3.62\nCn1cncc1c2c3C(=O)N(CC4CC4)C(=O)N(CC5CC5)c3nn2Cc6ccnc7ccc(Cl)cc67,\"InChI=1S/C27H26ClN7O2/c1-32-15-29-11-22(32)24-23-25(31-35(24)14-18-8-9-30-21-7-6-19(28)10-20(18)21)33(12-16-2-3-16)27(37)34(26(23)36)13-17-4-5-17/h6-11,15-17H,2-5,12-14H2,1H3\",[C][N][C][=N][C][=C][Ring1][Branch1][C][=C][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][C][C][Ring1][Ring1][C][Ring1][S][=N][N][Ring2][Ring1][Ring1][C][C][=C][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][O][Ring1][#Branch1],\"2-[(6-chloroquinolin-4-yl)methyl]-5,7-bis(cyclopropylmethyl)-3-(3-methylimidazol-4-yl)pyrazolo[4,3-e]pyrimidine-4,6-dione\",4.33\nOB1N(C(=O)Nc2ccccc12)c3ccccc3,\"InChI=1S/C13H11BN2O2/c17-13-15-12-9-5-4-8-11(12)14(18)16(13)10-6-2-1-3-7-10/h1-9,18H,(H,15,17)\",[O][B][N][Branch1][S][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-hydroxy-2-phenyl-4h-2,4,1-benzodiazaborinin-3-one\",1.4\nCC(C)N(CCC(C(=O)N)(c1ccccc1)c2ccccn2)C(C)C,\"InChI=1S/C21H29N3O/c1-16(2)24(17(3)4)15-13-21(20(22)25,18-10-6-5-7-11-18)19-12-8-9-14-23-19/h5-12,14,16-17H,13,15H2,1-4H3,(H2,22,25)\",[C][C][Branch1][C][C][N][Branch2][Ring1][=N][C][C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][C][C],4-(di(propan-2-yl)amino)-2-phenyl-2-pyridin-2-ylbutanamide,-0.54\nCC(Nc1ncnc2ccccc12)c3ccccc3,\"InChI=1S/C16H15N3/c1-12(13-7-3-2-4-8-13)19-16-14-9-5-6-10-15(14)17-11-18-16/h2-12H,1H3,(H,17,18,19)\",[C][C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-(1-phenylethyl)quinazolin-4-amine,3.4\nCC(C)c1ccc2Oc3nc(N)c(cc3C(=O)c2c1)C(=O)O,\"InChI=1S/C16H14N2O4/c1-7(2)8-3-4-12-9(5-8)13(19)10-6-11(16(20)21)14(17)18-15(10)22-12/h3-7H,1-2H3,(H2,17,18)(H,20,21)\",[C][C][Branch1][C][C][C][=C][C][=C][O][C][=N][C][Branch1][C][N][=C][Branch1][#C][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Ring1][N][=C][Ring1][S][C][=Branch1][C][=O][O],\"2-amino-5-oxo-7-propan-2-ylchromeno[3,2-e]pyridine-3-carboxylic acid\",1.1\nO[C@@H](CNCCCOCCOCCc1cccc2ccccc12)c3ccc(O)c4NC(=O)Sc34,\"InChI=1S/C26H30N2O5S/c29-22-10-9-21(25-24(22)28-26(31)34-25)23(30)17-27-12-4-13-32-15-16-33-14-11-19-7-3-6-18-5-1-2-8-20(18)19/h1-3,5-10,23,27,29-30H,4,11-17H2,(H,28,31)/t23-/m0/s1\",[O][C@@H1][Branch2][Ring1][#Branch2][C][N][C][C][C][O][C][C][O][C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-naphthalen-1-ylethoxy)ethoxy]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\",2.28\nCOc1ccccc1Cn2c(C)nc3ccccc23,\"InChI=1S/C16H16N2O/c1-12-17-14-8-4-5-9-15(14)18(12)11-13-7-3-6-10-16(13)19-2/h3-10H,11H2,1-2H3\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],1-[(2-methoxyphenyl)methyl]-2-methylbenzimidazole,3.47\nNC(Cc1c[nH]c2ccccc12)C(=O)O,\"InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)\",[N][C][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][O],2-amino-3-(1h-indol-3-yl)propanoic acid,-1.17\nN(c1ccccc1)c2cc(Nc3ccccc3)[nH]n2,\"InChI=1S/C15H14N4/c1-3-7-12(8-4-1)16-14-11-15(19-18-14)17-13-9-5-2-6-10-13/h1-11H,(H3,16,17,18,19)\",[N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][N][=Ring1][N],\"n,n'-di(phenyl)-1h-pyrazole-3,5-diamine\",3.8\nOC(C(=O)OC1CN2CCC1CC2)(c3ccccc3)c4ccccc4,\"InChI=1S/C21H23NO3/c23-20(25-19-15-22-13-11-16(19)12-14-22)21(24,17-7-3-1-4-8-17)18-9-5-2-6-10-18/h1-10,16,19,24H,11-15H2\",[O][C][Branch2][Ring1][C][C][=Branch1][C][=O][O][C][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-azabicyclo[2.2.2]octan-8-yl 2-hydroxy-2,2-di(phenyl)acetate\",1.19\nCc1ccccc1NC(=O)CCS(=O)(=O)c2ccc(Br)s2,\"InChI=1S/C14H14BrNO3S2/c1-10-4-2-3-5-11(10)16-13(17)8-9-21(18,19)14-7-6-12(15)20-14/h2-7H,8-9H2,1H3,(H,16,17)\",[C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][S][Ring1][=Branch1],3-(5-bromothiophen-2-yl)sulfonyl-n-(2-methylphenyl)propanamide,2.7\nO=C(COc1ccccc1)c2ccccc2,\"InChI=1S/C14H12O2/c15-14(12-7-3-1-4-8-12)11-16-13-9-5-2-6-10-13/h1-10H,11H2\",[O][=C][Branch1][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(phenoxy)-1-phenylethanone,2.87\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN4CCCC4,\"InChI=1S/C22H24ClFN4O2/c1-29-20-13-19-16(12-21(20)30-10-4-9-28-7-2-3-8-28)22(26-14-25-19)27-15-5-6-18(24)17(23)11-15/h5-6,11-14H,2-4,7-10H2,1H3,(H,25,26,27)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][C][C][C][C][Ring1][Branch1],n-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine,3.13\nClc1cccc2cn[nH]c12,\"InChI=1S/C7H5ClN2/c8-6-3-1-2-5-4-9-10-7(5)6/h1-4H,(H,9,10)\",[Cl][C][=C][C][=C][C][C][=N][NH1][C][Ring1][=Branch2][=Ring1][Branch1],7-chloro-1h-indazole,2.33\nClc1ccc(CN2CC3CNCC(C2)O3)cc1C(=O)NCC45CC6CC(CC(C6)C4)C5,\"InChI=1S/C25H34ClN3O2/c26-23-2-1-16(12-29-13-20-10-27-11-21(14-29)31-20)6-22(23)24(30)28-15-25-7-17-3-18(8-25)5-19(4-17)9-25/h1-2,6,17-21,27H,3-5,7-15H2,(H,28,30)\",[Cl][C][=C][C][=C][Branch1][P][C][N][C][C][C][N][C][C][Branch1][Ring2][C][Ring1][Branch2][O][Ring1][#Branch1][C][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],\"n-(1-adamantylmethyl)-2-chloro-5-(9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-ylmethyl)benzamide\",1.55\nCOc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(OC)n1,\"InChI=1S/C12H14N4O4S/c1-19-11-7-10(14-12(15-11)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16)\",[C][O][C][=C][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][=N][C][Branch1][Ring1][O][C][=N][Ring2][Ring1][Ring1],\"4-amino-n-(2,6-dimethoxypyrimidin-4-yl)benzenesulfonamide\",0.2\nC[C@H](Nc1ncc(F)c(Nc2cc([nH]n2)C3CC3)n1)c4ncc(F)cn4,\"InChI=1S/C16H16F2N8/c1-8(14-19-5-10(17)6-20-14)22-16-21-7-11(18)15(24-16)23-13-4-12(25-26-13)9-2-3-9/h4-9H,2-3H2,1H3,(H3,21,22,23,24,25,26)/t8-/m0/s1\",[C][C@H1][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][F][C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1],\"n'-(5-cyclopropyl-1h-pyrazol-3-yl)-5-fluoro-n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]pyrimidine-2,4-diamine\",2.47\nCOC(=O)c1ccc(C)c(NS(=O)(=O)c2ccc3N(C)SC(=O)c3c2)c1,\"InChI=1S/C17H16N2O5S2/c1-10-4-5-11(16(20)24-3)8-14(10)18-26(22,23)12-6-7-15-13(9-12)17(21)25-19(15)2/h4-9,18H,1-3H3\",[C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][Branch2][Ring1][N][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][N][Branch1][C][C][S][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][=C][Ring2][Ring1][=Branch1],\"methyl 4-methyl-3-[(1-methyl-3-oxo-2,1-benzothiazol-5-yl)sulfonylamino]benzoate\",2.6\nCOc1ccc(cc1)C2=COc3cc(O)cc(O)c3C2=O,\"InChI=1S/C16H12O5/c1-20-11-4-2-9(3-5-11)12-8-21-14-7-10(17)6-13(18)15(14)16(12)19/h2-8,17-18H,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][C][O][=C][C][Branch1][C][O][=C][Ring1][Branch2][C][Ring1][N][=O],\"5,7-dihydroxy-3-(4-methoxyphenyl)chromen-4-one\",3.5\nFc1cc(cc(F)c1C2=CCN(CC2)C=O)N3C[C@H](COc4ccon4)OC3=O,\"InChI=1S/C19H17F2N3O5/c20-15-7-13(8-16(21)18(15)12-1-4-23(11-25)5-2-12)24-9-14(29-19(24)26)10-27-17-3-6-28-22-17/h1,3,6-8,11,14H,2,4-5,9-10H2/t14-/m1/s1\",[F][C][=C][C][=Branch2][Ring1][Branch1][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=O][N][C][C@H1][Branch1][#Branch2][C][O][C][C][=C][O][N][=Ring1][Branch1][O][C][Ring1][N][=O],\"4-[2,6-difluoro-4-[(5r)-5-(1,2-oxazol-3-yloxymethyl)-2-oxo-1,3-oxazolidin-3-yl]phenyl]-3,6-dihydro-2h-pyridine-1-carbaldehyde\",2.01\nC[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc3ccccc3,\"InChI=1S/C22H25ClN2O4/c1-16-13-24(9-10-25(16)21(26)11-17-5-3-2-4-6-17)14-18-12-19(23)7-8-20(18)29-15-22(27)28/h2-8,12,16H,9-11,13-15H2,1H3,(H,27,28)/t16-/m0/s1\",[C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-chloro-2-[[(3s)-3-methyl-4-(2-phenylacetyl)piperazin-1-yl]methyl]phenoxy]acetic acid,0.18\nCc1cc(CCCOc2c(Cl)cc(cc2Cl)C3=NCCO3)on1,\"InChI=1S/C16H16Cl2N2O3/c1-10-7-12(23-20-10)3-2-5-21-15-13(17)8-11(9-14(15)18)16-19-4-6-22-16/h7-9H,2-6H2,1H3\",[C][C][C][=C][Branch2][Ring1][#Branch2][C][C][C][O][C][=C][Branch1][C][Cl][C][=C][Branch1][=Branch1][C][=C][Ring1][#Branch1][Cl][C][=N][C][C][O][Ring1][Branch1][O][N][=Ring2][Ring1][=Branch1],\"5-[3-[2,6-dichloro-4-(4,5-dihydro-1,3-oxazol-2-yl)phenoxy]propyl]-3-methyl-1,2-oxazole\",3.72\nCOc1ccc(Cc2c(N)n[nH]c2N)cc1,\"InChI=1S/C11H14N4O/c1-16-8-4-2-7(3-5-8)6-9-10(12)14-15-11(9)13/h2-5H,6H2,1H3,(H5,12,13,14,15)\",[C][O][C][=C][C][=C][Branch1][=N][C][C][C][Branch1][C][N][=N][NH1][C][=Ring1][=Branch1][N][C][=C][Ring1][=C],\"4-[(4-methoxyphenyl)methyl]-1h-pyrazole-3,5-diamine\",0.2\nCCN(CCN(C)C)S(=O)(=O)c1ccc(cc1)c2cnc(N)c(n2)C(=O)Nc3cccnc3,\"InChI=1S/C22H27N7O3S/c1-4-29(13-12-28(2)3)33(31,32)18-9-7-16(8-10-18)19-15-25-21(23)20(27-19)22(30)26-17-6-5-11-24-14-17/h5-11,14-15H,4,12-13H2,1-3H3,(H2,23,25)(H,26,30)\",[C][C][N][Branch1][Branch2][C][C][N][Branch1][C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1],3-amino-6-[4-(2-dimethylaminoethyl-ethylsulfamoyl)phenyl]-n-pyridin-3-ylpyrazine-2-carboxamide,2\nC1Oc2ccccc2C3=NN(CC13)c4ccccc4,\"InChI=1S/C16H14N2O/c1-2-6-13(7-3-1)18-10-12-11-19-15-9-5-4-8-14(15)16(12)17-18/h1-9,12H,10-11H2\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][N][Branch1][#Branch1][C][C][Ring1][=N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-phenyl-3a,4-dihydro-3h-chromeno[4,3-c]pyrazole\",4.28\nFC(F)c1nc2ccccc2[nH]1,\"InChI=1S/C8H6F2N2/c9-7(10)8-11-5-3-1-2-4-6(5)12-8/h1-4,7H,(H,11,12)\",[F][C][Branch1][C][F][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],2-(difluoromethyl)-1h-benzimidazole,2.02\nOc1ccccc1OC(=O)c2cccc3ccccc23,\"InChI=1S/C17H12O3/c18-15-10-3-4-11-16(15)20-17(19)14-9-5-7-12-6-1-2-8-13(12)14/h1-11,18H\",[O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],(2-hydroxyphenyl) naphthalene-1-carboxylate,4.4\nCOc1ccccc1CNc2cc(C)ccn2,\"InChI=1S/C14H16N2O/c1-11-7-8-15-14(9-11)16-10-12-5-3-4-6-13(12)17-2/h3-9H,10H2,1-2H3,(H,15,16)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][Branch1][C][C][=C][C][=N][Ring1][#Branch1],n-[(2-methoxyphenyl)methyl]-4-methylpyridin-2-amine,3.28\nNc1c2CCN(c3ccccc3)c2nc4ccc(Br)cc14,\"InChI=1S/C17H14BrN3/c18-11-6-7-15-14(10-11)16(19)13-8-9-21(17(13)20-15)12-4-2-1-3-5-12/h1-7,10H,8-9H2,(H2,19,20)\",[N][C][=C][C][C][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring2][Ring1][Ring2][Ring1][#Branch1],\"6-bromo-1-phenyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-amine\",3.12\nOC(C(=O)c1ccc(F)cc1)c2ccc(F)cc2,\"InChI=1S/C14H10F2O2/c15-11-5-1-9(2-6-11)13(17)14(18)10-3-7-12(16)8-4-10/h1-8,13,17H\",[O][C][Branch1][S][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"1,2-bis(4-fluorophenyl)-2-hydroxyethanone\",2.49\nCC(C)C[C@H](N)c1oc(nn1)S(=O)(=O)Cc2ccc(F)cc2,\"InChI=1S/C14H18FN3O3S/c1-9(2)7-12(16)13-17-18-14(21-13)22(19,20)8-10-3-5-11(15)6-4-10/h3-6,9,12H,7-8,16H2,1-2H3/t12-/m0/s1\",[C][C][Branch1][C][C][C][C@H1][Branch1][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"(1s)-1-[5-[(4-fluorophenyl)methylsulfonyl]-1,3,4-oxadiazol-2-yl]-3-methylbutan-1-amine\",1.11\nCC(C(Cc1nc2ccccc2[nH]1)c3nc4ccccc4[nH]3)c5ccccc5,\"InChI=1S/C24H22N4/c1-16(17-9-3-2-4-10-17)18(24-27-21-13-7-8-14-22(21)28-24)15-23-25-19-11-5-6-12-20(19)26-23/h2-14,16,18H,15H2,1H3,(H,25,26)(H,27,28)\",[C][C][Branch2][Ring1][#C][C][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[1-(1h-benzimidazol-2-yl)-3-phenylbutan-2-yl]-1h-benzimidazole,4.48\nClc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1,\"InChI=1S/C23H26ClN5O4/c24-15-1-3-19-18(11-15)29(22(31)14-33-19)10-9-28-7-5-16(6-8-28)25-12-17-2-4-20-23(26-17)27-21(30)13-32-20/h1-4,11,16,25H,5-10,12-14H2,(H,26,27,30)\",[Cl][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S],\"6-[[[1-[2-(6-chloro-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",1.33\nNC1(CCN(CC1)c2ncnc3[nH]ccc23)C(=O)NCc4ccc(Cl)cc4,\"InChI=1S/C19H21ClN6O/c20-14-3-1-13(2-4-14)11-23-18(27)19(21)6-9-26(10-7-19)17-15-5-8-22-16(15)24-12-25-17/h1-5,8,12H,6-7,9-11,21H2,(H,23,27)(H,22,24,25)\",[N][C][Branch2][Ring1][#Branch1][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=N][C][NH1][C][=C][C][Ring1][=Branch2][=Ring1][Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"4-amino-n-[(4-chlorophenyl)methyl]-1-(7h-pyrrolo[3,2-e]pyrimidin-4-yl)piperidine-4-carboxamide\",2.88\nCn1ncnc1COc2nn3c(nnc3cc2C(C)(C)C)c4cc(F)ccc4F,\"InChI=1S/C19H19F2N7O/c1-19(2,3)13-8-15-24-25-17(12-7-11(20)5-6-14(12)21)28(15)26-18(13)29-9-16-22-10-23-27(16)4/h5-8,10H,9H2,1-4H3\",[C][N][N][=C][N][=C][Ring1][Branch1][C][O][C][=N][N][C][=Branch2][Ring1][C][=N][N][=C][Ring1][Branch1][C][=C][Ring1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][F],\"7-tert-butyl-3-(2,5-difluorophenyl)-6-[(2-methyl-1,2,4-triazol-3-yl)methoxy]-[1,2,4]triazolo[3,4-f]pyridazine\",2.4\nCNCC[C@H](Oc1ccc(cc1)C(F)(F)F)c2ccccc2,\"InChI=1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3/t16-/m0/s1\",[C][N][C][C][C@H1][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1],(3s)-n-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine,1.89\nCc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)cc4Cl,\"InChI=1S/C24H29Cl2N3O4S/c1-17-2-5-21(6-3-17)34(31,32)27-24(30)29-12-8-19(9-13-29)28-14-10-20(11-15-28)33-23-7-4-18(25)16-22(23)26/h2-7,16,19-20H,8-15H2,1H3,(H,27,30)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl],\"4-[4-(2,4-dichlorophenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\",1.52\nO=C1C=COc2cc(OCc3ccccc3)ccc12,\"InChI=1S/C16H12O3/c17-15-8-9-18-16-10-13(6-7-14(15)16)19-11-12-4-2-1-3-5-12/h1-10H,11H2\",[O][=C][C][=C][O][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][C][Ring1][=C],7-(phenylmethoxy)chromen-4-one,3.33\n[O-][S+](c1ccccc1)c2ccc3nnnn3n2,InChI=1S/C10H7N5OS/c16-17(8-4-2-1-3-5-8)10-7-6-9-11-13-14-15(9)12-10/h1-7H,[O-1][S+1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=N][N][=N][N][Ring1][Branch1][N][=Ring1][=Branch2],\"6-phenylsulfinyltetrazolo[5,1-f]pyridazine\",0.79\n[O-][N+](=O)c1ccc2OC(CN(c2c1)c3cccc[n+]3[O-])(C(F)F)C(F)F,\"InChI=1S/C15H11F4N3O4/c16-13(17)15(14(18)19)8-20(12-3-1-2-6-21(12)23)10-7-9(22(24)25)4-5-11(10)26-15/h1-7,13-14H,8H2\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][O][C][Branch2][Ring1][Ring2][C][N][Branch1][#Branch1][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][C][=N+1][Ring1][=Branch1][O-1][Branch1][=Branch1][C][Branch1][C][F][F][C][Branch1][C][F][F],\"2,2-bis(difluoromethyl)-6-nitro-4-(1-oxidopyridin-1-ium-2-yl)-3h-1,4-benzoxazine\",3.2\nCC(C)NCC(O)COc1ccc(COCCOC(C)C)cc1,\"InChI=1S/C18H31NO4/c1-14(2)19-11-17(20)13-23-18-7-5-16(6-8-18)12-21-9-10-22-15(3)4/h5-8,14-15,17,19-20H,9-13H2,1-4H3\",[C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch1][O][C][O][C][C][O][C][Branch1][C][C][C][C][=C][Ring1][=C],1-(propan-2-ylamino)-3-[4-(2-propan-2-yloxyethoxymethyl)phenoxy]propan-2-ol,0.1\nCOc1ccc(cc1)C2=CC(=O)c3ccccc3N2,\"InChI=1S/C16H13NO2/c1-19-12-8-6-11(7-9-12)15-10-16(18)13-4-2-3-5-14(13)17-15/h2-10H,1H3,(H,17,18)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O],2-(4-methoxyphenyl)-1h-quinolin-4-one,2.71\nCN1SC(=NC1=O)NC(=O)c2cccc(Cl)c2,\"InChI=1S/C10H8ClN3O2S/c1-14-10(16)13-9(17-14)12-8(15)6-3-2-4-7(11)5-6/h2-5H,1H3,(H,12,13,15,16)\",[C][N][S][C][=Branch1][=Branch1][=N][C][Ring1][Branch1][=O][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],\"3-chloro-n-(2-methyl-3-oxo-1,2,4-thiadiazol-5-yl)benzamide\",0.87\nCC(=O)Nc1ccc(cc1)C(=O)Nc2ccccc2N,\"InChI=1S/C15H15N3O2/c1-10(19)17-12-8-6-11(7-9-12)15(20)18-14-5-3-2-4-13(14)16/h2-9H,16H2,1H3,(H,17,19)(H,18,20)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N],4-acetamido-n-(2-aminophenyl)benzamide,0.82\nOc1ccc2C(=O)C=C(Oc2c1)N3CCOCC3,\"InChI=1S/C13H13NO4/c15-9-1-2-10-11(16)8-13(18-12(10)7-9)14-3-5-17-6-4-14/h1-2,7-8,15H,3-6H2\",[O][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][O][N][C][C][O][C][C][Ring1][=Branch1],7-hydroxy-2-morpholin-4-ylchromen-4-one,1\nNC(=O)c1ccc(Oc2cccc3cccnc23)c(c1)[N+](=O)[O-],\"InChI=1S/C16H11N3O4/c17-16(20)11-6-7-13(12(9-11)19(21)22)23-14-5-1-3-10-4-2-8-18-15(10)14/h1-9H,(H2,17,20)\",[N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][Ring2][=C][Ring1][P][N+1][=Branch1][C][=O][O-1],3-nitro-4-quinolin-8-yloxybenzamide,1.7\nNc1ccc(cc1)S(=O)(=O)Nc2nccs2,\"InChI=1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)\",[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"4-amino-n-(1,3-thiazol-2-yl)benzenesulfonamide\",-0.37\nClc1ccc(cc1C(=O)NCC2CCCCC2)N3N=CC(=O)NC3=O,\"InChI=1S/C17H19ClN4O3/c18-14-7-6-12(22-17(25)21-15(23)10-20-22)8-13(14)16(24)19-9-11-4-2-1-3-5-11/h6-8,10-11H,1-5,9H2,(H,19,24)(H,21,23,25)\",[Cl][C][=C][C][=C][Branch2][Ring1][Ring1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Ring1][=Branch1][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O],\"2-chloro-n-(cyclohexylmethyl)-5-(3,5-dioxo-1,2,4-triazin-2-yl)benzamide\",1.26\nO=C(Oc1ccccc1)N2CCOCC2,\"InChI=1S/C11H13NO3/c13-11(12-6-8-14-9-7-12)15-10-4-2-1-3-5-10/h1-5H,6-9H2\",[O][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],phenyl morpholine-4-carboxylate,1.3\nFC(F)(F)c1nnc2ccc(nn12)N3CCCCC3,\"InChI=1S/C11H12F3N5/c12-11(13,14)10-16-15-8-4-5-9(17-19(8)10)18-6-2-1-3-7-18/h4-5H,1-3,6-7H2\",[F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][C][C][C][C][Ring1][=Branch1],\"6-piperidin-1-yl-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\",3\nCc1c(Sc2ccc(Cl)cc2)c3c(NS(=O)(=O)C)cccc3n1CC(=O)O,\"InChI=1S/C18H17ClN2O4S2/c1-11-18(26-13-8-6-12(19)7-9-13)17-14(20-27(2,24)25)4-3-5-15(17)21(11)10-16(22)23/h3-9,20H,10H2,1-2H3,(H,22,23)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Ring1][O][N][Ring2][Ring1][=Branch1][C][C][=Branch1][C][=O][O],2-[3-(4-chlorophenyl)sulfanyl-4-methanesulfonamido-2-methylindol-1-yl]acetic acid,0.21\nCCCNC(=O)CSc1ccc(cn1)S(=O)(=O)N2CCCC2,\"InChI=1S/C14H21N3O3S2/c1-2-7-15-13(18)11-21-14-6-5-12(10-16-14)22(19,20)17-8-3-4-9-17/h5-6,10H,2-4,7-9,11H2,1H3,(H,15,18)\",[C][C][C][N][C][=Branch1][C][=O][C][S][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1],n-propyl-2-(5-pyrrolidin-1-ylsulfonylpyridin-2-yl)sulfanylacetamide,1.55\nC[C@@H](Oc1cccc2ncnc(Nc3ccc4c(cnn4Cc5ccccn5)c3)c12)C(=O)N6CCOCC6,\"InChI=1S/C28H27N7O3/c1-19(28(36)34-11-13-37-14-12-34)38-25-7-4-6-23-26(25)27(31-18-30-23)33-21-8-9-24-20(15-21)16-32-35(24)17-22-5-2-3-10-29-22/h2-10,15-16,18-19H,11-14,17H2,1H3,(H,30,31,33)/t19-/m1/s1\",[C][C@@H1][Branch2][Ring2][=C][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][#Branch2][N][C][=C][C][=C][C][Branch1][#C][C][=N][N][Ring1][Branch1][C][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring1][S][=C][Ring2][Ring1][O][Ring2][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1],(2r)-1-morpholin-4-yl-2-[4-[[1-(pyridin-2-ylmethyl)indazol-5-yl]amino]quinazolin-5-yl]oxypropan-1-one,2.82\nCOc1ccc(Cn2cc3N(CC(C)C)C(=O)N(C)C(=O)c3c2)cc1,\"InChI=1S/C19H23N3O3/c1-13(2)9-22-17-12-21(10-14-5-7-15(25-4)8-6-14)11-16(17)18(23)20(3)19(22)24/h5-8,11-13H,9-10H2,1-4H3\",[C][O][C][=C][C][=C][Branch2][Ring1][S][C][N][C][=C][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=N][=C][Ring1][S][C][=C][Ring2][Ring1][#Branch1],\"6-[(4-methoxyphenyl)methyl]-3-methyl-1-(2-methylpropyl)pyrrolo[3,4-e]pyrimidine-2,4-dione\",3.52\nCOc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OCCn4cncn4,\"InChI=1S/C19H16ClFN6O2/c1-28-17-7-13-16(8-18(17)29-5-4-27-11-22-9-25-27)23-10-24-19(13)26-15-3-2-12(20)6-14(15)21/h2-3,6-11H,4-5H2,1H3,(H,23,24,26)\",[C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][C][=N][C][=N][Ring1][Branch1],\"n-(4-chloro-2-fluorophenyl)-6-methoxy-7-[2-(1,2,4-triazol-1-yl)ethoxy]quinazolin-4-amine\",3.2\nCCN1CCC[C@H]1CNC(=O)c2c(O)c(Cl)cc(Cl)c2OC,\"InChI=1S/C15H20Cl2N2O3/c1-3-19-6-4-5-9(19)8-18-15(21)12-13(20)10(16)7-11(17)14(12)22-2/h7,9,20H,3-6,8H2,1-2H3,(H,18,21)/t9-/m0/s1\",[C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][=Branch2][O][C],\"3,5-dichloro-n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2-hydroxy-6-methoxybenzamide\",1.09\nCC(=O)Nc1nc(C)c(s1)c2cnc(F)c(NS(=O)(=O)c3sc(C)nc3C)c2,\"InChI=1S/C16H16FN5O3S3/c1-7-13(27-16(20-7)21-9(3)23)11-5-12(14(17)18-6-11)22-28(24,25)15-8(2)19-10(4)26-15/h5-6,22H,1-4H3,(H,20,21,23)\",[C][C][=Branch1][C][=O][N][C][=N][C][Branch1][C][C][=C][Branch1][Ring2][S][Ring1][=Branch1][C][=C][N][=C][Branch1][C][F][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][S][C][Branch1][C][C][=N][C][=Ring1][=Branch1][C][=C][Ring2][Ring1][C],\"n-[5-[5-[(2,4-dimethyl-1,3-thiazol-5-yl)sulfonylamino]-6-fluoropyridin-3-yl]-4-methyl-1,3-thiazol-2-yl]acetamide\",0.55\nCSc1ncccc1C(=O)Nc2nccs2,\"InChI=1S/C10H9N3OS2/c1-15-9-7(3-2-4-11-9)8(14)13-10-12-5-6-16-10/h2-6H,1H3,(H,12,13,14)\",[C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"2-methylsulfanyl-n-(1,3-thiazol-2-yl)pyridine-3-carboxamide\",1.43\nCC1CC(CC(C)(C)C1)OC(=O)C(O)c2ccccc2,\"InChI=1S/C17H24O3/c1-12-9-14(11-17(2,3)10-12)20-16(19)15(18)13-7-5-4-6-8-13/h4-8,12,14-15,18H,9-11H2,1-3H3\",[C][C][C][C][Branch1][N][C][C][Branch1][C][C][Branch1][C][C][C][Ring1][Branch2][O][C][=Branch1][C][=O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(3,3,5-trimethylcyclohexyl) 2-hydroxy-2-phenylacetate\",2.31\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)C)C(=O)C(F)(F)F,\"InChI=1S/C20H22F3N3O5S/c1-12(2)17(18(28)20(21,22)23)24-16(27)11-26-15(13-7-5-4-6-8-13)10-9-14(19(26)29)25-32(3,30)31/h4-10,12,17,25H,11H2,1-3H3,(H,24,27)\",[C][C][Branch1][C][C][C][Branch2][Ring2][Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-(3-methanesulfonamido-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.77\nClc1ccc(CC2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C24H33ClN2O/c25-22-2-1-17(7-16-3-5-26-6-4-16)11-21(22)23(28)27-15-24-12-18-8-19(13-24)10-20(9-18)14-24/h1-2,11,16,18-20,26H,3-10,12-15H2,(H,27,28)\",[Cl][C][=C][C][=C][Branch1][#Branch2][C][C][C][C][N][C][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chloro-5-(piperidin-4-ylmethyl)benzamide,1.49\nCC[C@H](NC(=O)c1c(c(nc2ccccc12)c3ccccc3)S(=O)(=O)C)c4ccccc4,\"InChI=1S/C26H24N2O3S/c1-3-21(18-12-6-4-7-13-18)28-26(29)23-20-16-10-11-17-22(20)27-24(25(23)32(2,30)31)19-14-8-5-9-15-19/h4-17,21H,3H2,1-2H3,(H,28,29)/t21-/m0/s1\",[C][C][C@H1][Branch2][Ring2][=Branch2][N][C][=Branch1][C][=O][C][=C][Branch2][Ring1][#Branch1][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],3-methylsulfonyl-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,3.17\nFc1ccc(NC(=O)c2cccnc2Oc3ccccc3)cc1,\"InChI=1S/C18H13FN2O2/c19-13-8-10-14(11-9-13)21-17(22)16-7-4-12-20-18(16)23-15-5-2-1-3-6-15/h1-12H,(H,21,22)\",[F][C][=C][C][=C][Branch2][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],n-(4-fluorophenyl)-2-(phenoxy)pyridine-3-carboxamide,3.19\nCC(CN1CCCCC1)C(=O)c2ccc(C)cc2,\"InChI=1S/C16H23NO/c1-13-6-8-15(9-7-13)16(18)14(2)12-17-10-4-3-5-11-17/h6-9,14H,3-5,10-12H2,1-2H3\",[C][C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],2-methyl-1-(4-methylphenyl)-3-piperidin-1-ylpropan-1-one,1.65\nCC(C)OC(=O)N1CCC(CC1)Oc2ncnc(Nc3ccc(nc3C)S(=O)(=O)C)c2C,\"InChI=1S/C21H29N5O5S/c1-13(2)30-21(27)26-10-8-16(9-11-26)31-20-14(3)19(22-12-23-20)25-17-6-7-18(24-15(17)4)32(5,28)29/h6-7,12-13,16H,8-11H2,1-5H3,(H,22,23,25)\",[C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][N][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Ring2][Ring1][C][C],propan-2-yl 4-[5-methyl-6-[(2-methyl-6-methylsulfonylpyridin-3-yl)amino]pyrimidin-4-yl]oxypiperidine-1-carboxylate,2.8\nCSc1ccc(cc1)N2C(=NC(=NC2(C)C)N)N,\"InChI=1S/C12H17N5S/c1-12(2)16-10(13)15-11(14)17(12)8-4-6-9(18-3)7-5-8/h4-7H,1-3H3,(H4,13,14,15,16)\",[C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][=C][=N][C][=Branch1][=Branch2][=N][C][Ring1][=Branch1][Branch1][C][C][C][N][N],\"6,6-dimethyl-1-(4-methylsulfanylphenyl)-1,3,5-triazine-2,4-diamine\",-0.84\nNc1nc(N)nc(n1)c2cccc(c2)C(F)(F)F,\"InChI=1S/C10H8F3N5/c11-10(12,13)6-3-1-2-5(4-6)7-16-8(14)18-9(15)17-7/h1-4H,(H4,14,15,16,17,18)\",[N][C][=N][C][Branch1][C][N][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"6-[3-(trifluoromethyl)phenyl]-1,3,5-triazine-2,4-diamine\",2.4\nCc1cccc(CN2CCN(CC2)C(c3ccccc3)c4ccc(Cl)cc4)c1,\"InChI=1S/C25H27ClN2/c1-20-6-5-7-21(18-20)19-27-14-16-28(17-15-27)25(22-8-3-2-4-9-22)23-10-12-24(26)13-11-23/h2-13,18,25H,14-17,19H2,1H3\",[C][C][=C][C][=C][C][Branch2][Ring2][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][O],1-[(4-chlorophenyl)-phenylmethyl]-4-[(3-methylphenyl)methyl]piperazine,3.39\nFc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C23H26Cl2FN3O4S/c24-21-6-3-19(15-22(21)25)33-18-9-13-28(14-10-18)17-7-11-29(12-8-17)23(30)27-34(31,32)20-4-1-16(26)2-5-20/h1-6,15,17-18H,7-14H2,(H,27,30)\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(4-fluorophenyl)sulfonylpiperidine-1-carboxamide\",1.79\nOC(=O)COc1ccc(Cl)cc1CN2CCCN(CC2)S(=O)(=O)Cc3ccccc3,\"InChI=1S/C21H25ClN2O5S/c22-19-7-8-20(29-15-21(25)26)18(13-19)14-23-9-4-10-24(12-11-23)30(27,28)16-17-5-2-1-3-6-17/h1-3,5-8,13H,4,9-12,14-16H2,(H,25,26)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[4-chloro-2-[[4-(phenylmethylsulfonyl)-1,4-diazepan-1-yl]methyl]phenoxy]acetic acid\",1.01\nCN1CCCN(CC1)C(c2ccccc2)c3ccc(Cl)cc3,\"InChI=1S/C19H23ClN2/c1-21-12-5-13-22(15-14-21)19(16-6-3-2-4-7-16)17-8-10-18(20)11-9-17/h2-4,6-11,19H,5,12-15H2,1H3\",[C][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"1-[(4-chlorophenyl)-phenylmethyl]-4-methyl-1,4-diazepane\",2.36\nClc1ccccc1CCNC(=O)c2cc(ccc2Cl)N3N=CC(=O)NC3=O,\"InChI=1S/C18H14Cl2N4O3/c19-14-4-2-1-3-11(14)7-8-21-17(26)13-9-12(5-6-15(13)20)24-18(27)23-16(25)10-22-24/h1-6,9-10H,7-8H2,(H,21,26)(H,23,25,27)\",[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O],\"2-chloro-n-[2-(2-chlorophenyl)ethyl]-5-(3,5-dioxo-1,2,4-triazin-2-yl)benzamide\",1.29\nClc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4ccccn4)C3=O,\"InChI=1S/C17H11ClN4O3/c18-9-4-5-11-12(7-9)20-14-13(15(11)23)17(25)22(21-16(14)24)8-10-3-1-2-6-19-10/h1-7H,8H2,(H,20,23)(H,21,24)\",[Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][#Branch2][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Ring1][P][=O],\"7-chloro-2-(pyridin-2-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",1.1\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)N)C(=O)C(F)(F)F,\"InChI=1S/C19H21F3N4O5S/c1-11(2)16(17(28)19(20,21)22)24-15(27)10-26-14(12-6-4-3-5-7-12)9-8-13(18(26)29)25-32(23,30)31/h3-9,11,16,25H,10H2,1-2H3,(H,24,27)(H2,23,30,31)\",[C][C][Branch1][C][C][C][Branch2][Ring2][Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-6-phenyl-3-(sulfamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.17\nOC(=O)C1CCN(CC1)c2ncccc2c3ccc(Cl)c(c3)C(=O)NCC4CCCCCC4,\"InChI=1S/C26H32ClN3O3/c27-23-10-9-20(16-22(23)25(31)29-17-18-6-3-1-2-4-7-18)21-8-5-13-28-24(21)30-14-11-19(12-15-30)26(32)33/h5,8-10,13,16,18-19H,1-4,6-7,11-12,14-15,17H2,(H,29,31)(H,32,33)\",[O][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][C][Ring1][#Branch1],1-[3-[4-chloro-3-(cycloheptylmethylcarbamoyl)phenyl]pyridin-2-yl]piperidine-4-carboxylic acid,2.53\nO=C(NCCSCc1ccccc1)c2ccccc2,\"InChI=1S/C16H17NOS/c18-16(15-9-5-2-6-10-15)17-11-12-19-13-14-7-3-1-4-8-14/h1-10H,11-13H2,(H,17,18)\",[O][=C][Branch1][=C][N][C][C][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-[2-(phenylmethylsulfanyl)ethyl]benzamide,3.3\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3c[nH]c4ccccc34)c2C(=O)N5CC[C@@H](O)C5,\"InChI=1S/C25H28N4O4S/c1-14(2)12-29-24-21(22(31)27(3)25(29)33)20(23(32)28-9-8-16(30)13-28)19(34-24)10-15-11-26-18-7-5-4-6-17(15)18/h4-7,11,14,16,26,30H,8-10,12-13H2,1-3H3/t16-/m1/s1\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][=C][Ring1][#C][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1],\"5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-6-(1h-indol-3-ylmethyl)-3-methyl-1-(2-methylpropyl)thieno[3,2-e]pyrimidine-2,4-dione\",2.35\nC(CN1CCCCC1)C2CCc3cc(OCc4ccc(cc4)c5ccccc5)ccc3C2,\"InChI=1S/C30H35NO/c1-3-7-26(8-4-1)27-12-10-25(11-13-27)23-32-30-16-15-28-21-24(9-14-29(28)22-30)17-20-31-18-5-2-6-19-31/h1,3-4,7-8,10-13,15-16,22,24H,2,5-6,9,14,17-21,23H2\",[C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][=C][C][Branch2][Ring1][Branch1][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Ring2][C][Ring2][Ring1][Branch2],\"1-[2-[6-[(4-phenylphenyl)methoxy]-1,2,3,4-tetrahydronaphthalen-2-yl]ethyl]piperidine\",3.3\nCCCNC[C@@H](O)COc1ccccc1C(=O)CCc2ccccc2,\"InChI=1S/C21H27NO3/c1-2-14-22-15-18(23)16-25-21-11-7-6-10-19(21)20(24)13-12-17-8-4-3-5-9-17/h3-11,18,22-23H,2,12-16H2,1H3/t18-/m1/s1\",[C][C][C][N][C][C@@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],1-[2-[(2r)-2-hydroxy-3-propylaminopropoxy]phenyl]-3-phenylpropan-1-one,1.56\nO=C(CCc1ccccc1)c2ccccc2,\"InChI=1S/C15H14O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-10H,11-12H2\",[O][=C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1,3-di(phenyl)propan-1-one\",3.77\nCCCCc1ncc(\\C=C(/Cc2cccs2)\\C(=O)O)n1Cc3ccc(cc3)C(=O)O,\"InChI=1S/C23H24N2O4S/c1-2-3-6-21-24-14-19(12-18(23(28)29)13-20-5-4-11-30-20)25(21)15-16-7-9-17(10-8-16)22(26)27/h4-5,7-12,14H,2-3,6,13,15H2,1H3,(H,26,27)(H,28,29)/b18-12+\",[C][C][C][C][C][=N][C][=C][Branch2][Ring1][C][\\C][=C][Branch1][=Branch2][/C][C][=C][C][=C][S][Ring1][Branch1][\\C][=Branch1][C][=O][O][N][Ring1][S][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O],4-[[2-butyl-5-[(e)-3-hydroxy-3-oxo-2-(thiophen-2-ylmethyl)prop-1-enyl]imidazol-1-yl]methyl]benzoic acid,-0.9\nC(C(C1CCCCC1)C2CCCCC2)C3CCCCN3,\"InChI=1S/C19H35N/c1-3-9-16(10-4-1)19(17-11-5-2-6-12-17)15-18-13-7-8-14-20-18/h16-20H,1-15H2\",[C][Branch2][Ring1][Ring2][C][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][C][N][Ring1][=Branch1],\"2-(2,2-dicyclohexylethyl)piperidine\",3.02\nO=C(Nc1nc2C(=O)NC=Nc2s1)c3ccccc3,\"InChI=1S/C12H8N4O2S/c17-9(7-4-2-1-3-5-7)16-12-15-8-10(18)13-6-14-11(8)19-12/h1-6H,(H,13,14,18)(H,15,16,17)\",[O][=C][Branch2][Ring1][C][N][C][=N][C][C][=Branch1][C][=O][N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-(7-oxo-6h-[1,3]thiazolo[5,4-d]pyrimidin-2-yl)benzamide\",1.94\nCOc1cccc([C@H](O)C2CCN(CCc3ccc(F)cc3)CC2)c1OC,\"InChI=1S/C22H28FNO3/c1-26-20-5-3-4-19(22(20)27-2)21(25)17-11-14-24(15-12-17)13-10-16-6-8-18(23)9-7-16/h3-9,17,21,25H,10-15H2,1-2H3/t21-/m1/s1\",[C][O][C][=C][C][=C][C][Branch2][Ring1][N][C@H1][Branch1][C][O][C][C][C][N][Branch1][=C][C][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring1][#C][=C][Ring2][Ring1][#Branch1][O][C],\"(r)-(2,3-dimethoxyphenyl)-[1-[2-(4-fluorophenyl)ethyl]piperidin-4-yl]methanol\",1.7\nO=C(COc1ccccc1)N2CCOCC2,\"InChI=1S/C12H15NO3/c14-12(13-6-8-15-9-7-13)10-16-11-4-2-1-3-5-11/h1-5H,6-10H2\",[O][=C][Branch1][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],1-morpholin-4-yl-2-(phenoxy)ethanone,0.75\nCc1nnsc1C(=O)Nc2ccccc2,\"InChI=1S/C10H9N3OS/c1-7-9(15-13-12-7)10(14)11-8-5-3-2-4-6-8/h2-6H,1H3,(H,11,14)\",[C][C][N][=N][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],4-methyl-n-phenylthiadiazole-5-carboxamide,0.97\nCC[C@H](C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@@H]12,\"InChI=1S/C24H38O6/c1-5-15(3)24(29)30-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-18(25)12-19(26)13-22(27)28/h6-7,10,14-16,18-21,23,25-26H,5,8-9,11-13H2,1-4H3,(H,27,28)/t14-,15-,16-,18+,19+,20-,21-,23-/m0/s1\",[C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@@H1][Branch1][C][C][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch2][Ring1][C][C][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][C@@H1][Ring2][Ring1][#Branch1][Ring2][Ring1][C],\"(3r,5r)-7-[(1s,2s,6r,8s,8ar)-2,6-dimethyl-8-[(2s)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid\",1.07\nCOc1cc(O)cc2OC=C(C(=O)c12)c3ccc(O)cc3,\"InChI=1S/C16H12O5/c1-20-13-6-11(18)7-14-15(13)16(19)12(8-21-14)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3\",[C][O][C][=C][C][Branch1][C][O][=C][C][O][C][=C][Branch1][#Branch2][C][=Branch1][C][=O][C][Ring1][N][=Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],7-hydroxy-3-(4-hydroxyphenyl)-5-methoxychromen-4-one,2\nO=C(C1CCCCC1)N2CC3N(CCc4ccccc34)C(=O)C2,\"InChI=1S/C19H24N2O2/c22-18-13-20(19(23)15-7-2-1-3-8-15)12-17-16-9-5-4-6-14(16)10-11-21(17)18/h4-6,9,15,17H,1-3,7-8,10-13H2\",[O][=C][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][N][C][C][N][Branch1][=N][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring1][#C],\"2-(cyclohexanecarbonyl)-3,6,7,11b-tetrahydro-1h-pyrazino[6,1-a]isoquinolin-4-one\",2.43\nNc1cc(nc2ccc(Nc3cc(nc(N)n3)c4cccc(Cl)c4)cc12)c5ccc(F)cc5,\"InChI=1S/C25H18ClFN6/c26-16-3-1-2-15(10-16)23-13-24(33-25(29)32-23)30-18-8-9-21-19(11-18)20(28)12-22(31-21)14-4-6-17(27)7-5-14/h1-13H,(H2,28,31)(H3,29,30,32,33)\",[N][C][=C][C][=Branch2][Ring2][#Branch2][=N][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][=C][C][=Branch1][=Branch2][=N][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"n'-[2-amino-6-(3-chlorophenyl)pyrimidin-4-yl]-2-(4-fluorophenyl)quinoline-4,6-diamine\",2.5\nFc1ccc(SC2=NN3C=NC(=O)C(=C3C=C2)c4c(Cl)cccc4Cl)c(F)c1,InChI=1S/C19H9Cl2F2N3OS/c20-11-2-1-3-12(21)17(11)18-14-5-7-16(25-26(14)9-24-19(18)27)28-15-6-4-10(22)8-13(15)23/h1-9H,[F][C][=C][C][=C][Branch2][Ring1][P][S][C][=N][N][C][=N][C][=Branch1][C][=O][C][=Branch1][Branch2][=C][Ring1][#Branch1][C][=C][Ring1][O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][Branch1][C][F][=C][Ring2][Ring1][O],\"5-(2,6-dichlorophenyl)-2-(2,4-difluorophenyl)sulfanylpyridazino[6,1-f]pyrimidin-6-one\",2.74\nNC(=O)c1sc(cc1N)c2ccccc2,\"InChI=1S/C11H10N2OS/c12-8-6-9(15-10(8)11(13)14)7-4-2-1-3-5-7/h1-6H,12H2,(H2,13,14)\",[N][C][=Branch1][C][=O][C][S][C][=Branch1][=Branch1][=C][C][=Ring1][Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],3-amino-5-phenylthiophene-2-carboxamide,2.33\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4cc(Cl)ccc34,\"InChI=1S/C21H17ClN2O2/c1-12-3-6-19-17(9-12)21(13(2)24(19)11-20(25)26)16-7-8-23-18-10-14(22)4-5-15(16)18/h3-10H,11H2,1-2H3,(H,25,26)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1],\"2-[3-(7-chloroquinolin-4-yl)-2,5-dimethylindol-1-yl]acetic acid\",1.59\nCOc1ccc2ncc(F)c(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2n1,\"InChI=1S/C24H28FN5O3/c1-31-23-3-2-20-24(29-23)18(19(25)14-28-20)6-9-30-7-4-16(5-8-30)26-13-17-12-21-22(15-27-17)33-11-10-32-21/h2-3,12,14-16,26H,4-11,13H2,1H3\",[C][O][C][=C][C][=C][N][=C][C][Branch1][C][F][=C][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=N][Ring2][Ring1][#C],\"n-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethyl)-1-[2-(3-fluoro-6-methoxy-1,5-naphthyridin-4-yl)ethyl]piperidin-4-amine\",1.46\nClc1ccc2OC(=O)Nc2c1,\"InChI=1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)\",[Cl][C][=C][C][=C][O][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"5-chloro-3h-1,3-benzoxazol-2-one\",2.16\nOC(=O)COc1ccc(cc1CN2CCN(CC2)S(=O)(=O)c3ccccc3)C(F)(F)F,\"InChI=1S/C20H21F3N2O5S/c21-20(22,23)16-6-7-18(30-14-19(26)27)15(12-16)13-24-8-10-25(11-9-24)31(28,29)17-4-2-1-3-5-17/h1-7,12H,8-11,13-14H2,(H,26,27)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],2-[2-[(4-phenylsulfonylpiperazin-1-yl)methyl]-4-(trifluoromethyl)phenoxy]acetic acid,0.4\n[O-][N+](=O)c1cccc(c1)C(=O)Nc2nc3ccccc3n2CCN4CCOCC4,\"InChI=1S/C20H21N5O4/c26-19(15-4-3-5-16(14-15)25(27)28)22-20-21-17-6-1-2-7-18(17)24(20)9-8-23-10-12-29-13-11-23/h1-7,14H,8-13H2,(H,21,22,26)\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][N][C][C][O][C][C][Ring1][=Branch1],n-[1-(2-morpholin-4-ylethyl)benzimidazol-2-yl]-3-nitrobenzamide,3.3\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2cccnc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C26H25F3N4O5/c1-16(2)22(23(35)26(27,28)29)32-21(34)14-33-20(18-9-6-12-30-13-18)11-10-19(24(33)36)31-25(37)38-15-17-7-4-3-5-8-17/h3-13,16,22H,14-15H2,1-2H3,(H,31,37)(H,32,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-pyridin-3-ylpyridin-3-yl]carbamate\",3.05\nCOc1ccc2nccc([C@H](O)C3CC4CCN3CC4C=C)c2c1,\"InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13?,14?,19?,20-/m0/s1\",[C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Ring1][C@H1][Branch1][C][O][C][C][C][C][C][N][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1],(s)-(5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol,2.16\nClc1ccc(Cl)c(c1)S(=O)(=O)Nc2nccs2,\"InChI=1S/C9H6Cl2N2O2S2/c10-6-1-2-7(11)8(5-6)17(14,15)13-9-12-3-4-16-9/h1-5H,(H,12,13)\",[Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"2,5-dichloro-n-(1,3-thiazol-2-yl)benzenesulfonamide\",1.14\nCc1cc(C(=O)CN2C=C(C=CC2=O)C(F)(F)F)c(C)n1Cc3ccccc3,\"InChI=1S/C21H19F3N2O2/c1-14-10-18(15(2)26(14)11-16-6-4-3-5-7-16)19(27)13-25-12-17(21(22,23)24)8-9-20(25)28/h3-10,12H,11,13H2,1-2H3\",[C][C][=C][C][Branch2][Ring1][=Branch2][C][=Branch1][C][=O][C][N][C][=C][Branch1][#Branch1][C][=C][C][Ring1][=Branch1][=O][C][Branch1][C][F][Branch1][C][F][F][=C][Branch1][C][C][N][Ring2][Ring1][Ring2][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-[2-[2,5-dimethyl-1-(phenylmethyl)pyrrol-3-yl]-2-oxoethyl]-5-(trifluoromethyl)pyridin-2-one\",3.46\nOc1ccc2nc(sc2c1)c3ccccc3,\"InChI=1S/C13H9NOS/c15-10-6-7-11-12(8-10)16-13(14-11)9-4-2-1-3-5-9/h1-8,15H\",[O][C][=C][C][=C][N][=C][Branch1][Branch2][S][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-phenyl-1,3-benzothiazol-6-ol\",3.99\nNS(=O)(=O)c1nc2ccccc2s1,\"InChI=1S/C7H6N2O2S2/c8-13(10,11)7-9-5-3-1-2-4-6(5)12-7/h1-4H,(H2,8,10,11)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2],\"1,3-benzothiazole-2-sulfonamide\",1.35\nOC[C@H]1C[C@H]([C@H](O)[C@@H]1O)n2nnc3c(N[C@@H]4C[C@H]4c5ccc(F)c(F)c5)nc(SCCC(F)(F)F)nc23,\"InChI=1S/C22H23F5N6O3S/c23-12-2-1-9(5-13(12)24)11-7-14(11)28-19-16-20(30-21(29-19)37-4-3-22(25,26)27)33(32-31-16)15-6-10(8-34)17(35)18(15)36/h1-2,5,10-11,14-15,17-18,34-36H,3-4,6-8H2,(H,28,29,30)/t10-,11+,14-,15-,17-,18+/m1/s1\",[O][C][C@H1][C][C@H1][Branch1][=Branch2][C@H1][Branch1][C][O][C@@H1][Ring1][=Branch1][O][N][N][=N][C][=C][Branch2][Ring1][Branch1][N][C@@H1][C][C@H1][Ring1][Ring1][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2][N][=C][Branch1][N][S][C][C][C][Branch1][C][F][Branch1][C][F][F][N][=C][Ring2][Ring1][N][Ring2][Ring1][=Branch2],\"(1r,2s,3r,5r)-3-[7-[[(1r,2s)-2-(3,4-difluorophenyl)cyclopropyl]amino]-5-(3,3,3-trifluoropropylsulfanyl)triazolo[5,4-d]pyrimidin-3-yl]-5-(hydroxymethyl)cyclopentane-1,2-diol\",3.99\nNC(=O)c1ccccc1OCc2ccccc2,\"InChI=1S/C14H13NO2/c15-14(16)12-8-4-5-9-13(12)17-10-11-6-2-1-3-7-11/h1-9H,10H2,(H2,15,16)\",[N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(phenylmethoxy)benzamide,2.5\nCC1CC(=O)Nc2ccccc2N1,\"InChI=1S/C10H12N2O/c1-7-6-10(13)12-9-5-3-2-4-8(9)11-7/h2-5,7,11H,6H2,1H3,(H,12,13)\",[C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][N],\"2-methyl-1,2,3,5-tetrahydro-1,5-benzodiazepin-4-one\",0.56\nNC(=O)N1c2ccccc2CC(=O)c3ccccc13,\"InChI=1S/C15H12N2O2/c16-15(19)17-12-7-3-1-5-10(12)9-14(18)11-6-2-4-8-13(11)17/h1-8H,9H2,(H2,16,19)\",[N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1],5-oxo-6h-benzo[b][1]benzazepine-11-carboxamide,1.28\nCOc1ccc(cc1OC)C2=COc3cc(O)cc(O)c3C2=O,\"InChI=1S/C17H14O6/c1-21-13-4-3-9(5-14(13)22-2)11-8-23-15-7-10(18)6-12(19)16(15)17(11)20/h3-8,18-19H,1-2H3\",[C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=C][O][C][=C][C][Branch1][C][O][=C][C][Branch1][C][O][=C][Ring1][Branch2][C][Ring1][N][=O],\"3-(3,4-dimethoxyphenyl)-5,7-dihydroxychromen-4-one\",2.8\nCC(=O)Nc1ccc2c(c1)c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O,\"InChI=1S/C19H17ClN2O3S/c1-11-19(26-15-6-3-13(20)4-7-15)16-9-14(21-12(2)23)5-8-17(16)22(11)10-18(24)25/h3-9H,10H2,1-2H3,(H,21,23)(H,24,25)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O],2-[5-acetamido-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid,0.2\nO[C@@H](CNCCSCCCNCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H29N3O3S2/c26-18-8-7-17(21-20(18)25-22(28)30-21)19(27)15-24-12-14-29-13-4-10-23-11-9-16-5-2-1-3-6-16/h1-3,5-8,19,23-24,26-27H,4,9-15H2,(H,25,28)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(2-phenylethylamino)propylsulfanyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\",0.12\nC[C@]1(CCCN1c2nc(Nc3cc([nH]n3)C4CC4)c5cccn5n2)C(=O)Nc6ccc(F)nc6,\"InChI=1S/C23H24FN9O/c1-23(21(34)26-15-7-8-18(24)25-13-15)9-3-10-32(23)22-28-20(17-4-2-11-33(17)31-22)27-19-12-16(29-30-19)14-5-6-14/h2,4,7-8,11-14H,3,5-6,9-10H2,1H3,(H,26,34)(H2,27,28,29,30,31)/t23-/m0/s1\",[C][C@][Branch2][Ring2][=Branch1][C][C][C][N][Ring1][Branch1][C][N][=C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][C][=C][C][=C][N][Ring1][Branch1][N][=Ring2][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][N][=C][Ring1][#Branch1],\"(2s)-1-[4-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]pyrrolo[2,1-f][1,2,4]triazin-2-yl]-n-(6-fluoropyridin-3-yl)-2-methylpyrrolidine-2-carboxamide\",3.16\nCC1CN(C(=O)c2ccccc2)c3ccccc3NC1=O,\"InChI=1S/C17H16N2O2/c1-12-11-19(17(21)13-7-3-2-4-8-13)15-10-6-5-9-14(15)18-16(12)20/h2-10,12H,11H2,1H3,(H,18,20)\",[C][C][C][N][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring2][Ring1][Ring1][=O],\"1-(benzoyl)-3-methyl-3,5-dihydro-2h-1,5-benzodiazepin-4-one\",1.73\nO[C@@H](CNCCCSCCNCCc1cccc(Cl)c1Cl)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H27Cl2N3O3S2/c23-16-4-1-3-14(19(16)24)7-9-25-10-12-31-11-2-8-26-13-18(29)15-5-6-17(28)20-21(15)32-22(30)27-20/h1,3-6,18,25-26,28-29H,2,7-13H2,(H,27,30)/t18-/m0/s1\",[O][C@@H1][Branch2][Ring1][Branch2][C][N][C][C][C][S][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"7-[(1r)-2-[3-[2-[2-(2,3-dichlorophenyl)ethylamino]ethylsulfanyl]propylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",1.74\nNC(=O)Nc1cc(sc1C(=O)N[C@H]2CCCNC2)c3cccc(F)c3F,\"InChI=1S/C17H18F2N4O2S/c18-11-5-1-4-10(14(11)19)13-7-12(23-17(20)25)15(26-13)16(24)22-9-3-2-6-21-8-9/h1,4-5,7,9,21H,2-3,6,8H2,(H,22,24)(H3,20,23,25)/t9-/m0/s1\",[N][C][=Branch1][C][=O][N][C][C][=C][Branch2][Ring1][C][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F],\"3-(carbamoylamino)-5-(2,3-difluorophenyl)-n-[(3s)-piperidin-3-yl]thiophene-2-carboxamide\",1.32\nCC(C)C(=O)Nc1nc(cc2ccccc12)c3ccccn3,\"InChI=1S/C18H17N3O/c1-12(2)18(22)21-17-14-8-4-3-7-13(14)11-16(20-17)15-9-5-6-10-19-15/h3-12H,1-2H3,(H,20,21,22)\",[C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=N][C][=Branch1][N][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1],2-methyl-n-(3-pyridin-2-ylisoquinolin-1-yl)propanamide,2.7\nNc1nc(N)c2nc(c(N)nc2n1)c3ccccc3,\"InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)\",[N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][N][C][Branch1][C][N][=N][C][Ring1][#Branch1][=N][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"6-phenylpteridine-2,4,7-triamine\",1.16\nC[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)NCC=C)C(F)(F)F,\"InChI=1S/C13H14ClF3N2O4S/c1-3-6-18-24(22,23)8-4-5-10(9(14)7-8)19-11(20)12(2,21)13(15,16)17/h3-5,7,18,21H,1,6H2,2H3,(H,19,20)/t12-/m1/s1\",[C][C@@][Branch1][C][O][Branch2][Ring1][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][=C][C][Branch1][C][F][Branch1][C][F][F],\"(2r)-n-[2-chloro-4-(prop-2-enylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",3.07\nNC12CC3CC(CC(C3)C1)C2,\"InChI=1S/C10H17N/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2\",[N][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],adamantan-1-amine,-0.98\nO=C1Nc2ccccc2C(=O)C=C1,\"InChI=1S/C10H7NO2/c12-9-5-6-10(13)11-8-4-2-1-3-7(8)9/h1-6H,(H,11,13)\",[O][=C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][Ring1][N],\"1h-1-benzazepine-2,5-dione\",1.02\nCC[C@@H](NC1=C(Nc2cccc(C(=O)N(C)C)c2O)C(=O)C1=O)c3oc(C)cc3,\"InChI=1S/C21H23N3O5/c1-5-13(15-10-9-11(2)29-15)22-16-17(20(27)19(16)26)23-14-8-6-7-12(18(14)25)21(28)24(3)4/h6-10,13,22-23,25H,5H2,1-4H3/t13-/m1/s1\",[C][C][C@@H1][Branch2][Ring2][Branch1][N][C][=C][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][Branch1][#Branch2][C][=Branch1][C][=O][N][Branch1][C][C][C][=C][Ring1][O][O][C][=Branch1][C][=O][C][Ring2][Ring1][C][=O][C][O][C][Branch1][C][C][=C][C][=Ring1][=Branch1],\"2-hydroxy-n,n-dimethyl-3-[[2-[[(1r)-1-(5-methylfuran-2-yl)propyl]amino]-3,4-dioxo-1-cyclobutenyl]amino]benzamide\",2.32\nCC[C@H](NC(=O)c1c(CN(C)C)c(nc2ccccc12)c3ccccc3)c4ccccc4,\"InChI=1S/C28H29N3O/c1-4-24(20-13-7-5-8-14-20)30-28(32)26-22-17-11-12-18-25(22)29-27(23(26)19-31(2)3)21-15-9-6-10-16-21/h5-18,24H,4,19H2,1-3H3,(H,30,32)/t24-/m0/s1\",[C][C][C@H1][Branch2][Ring2][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][C][N][Branch1][C][C][C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-(dimethylaminomethyl)-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,4.18\nNc1nc(cs1)c2ccccc2,\"InChI=1S/C9H8N2S/c10-9-11-8(6-12-9)7-4-2-1-3-5-7/h1-6H,(H2,10,11)\",[N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4-phenyl-1,3-thiazol-2-amine\",2.43\nNc1nnc(c(N)n1)c2cccc(Cl)c2Cl,\"InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16)\",[N][C][=N][N][=C][Branch1][Branch2][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl],\"6-(2,3-dichlorophenyl)-1,2,4-triazine-3,5-diamine\",1.38\nCCOC(=O)C(CCc1ccccc1)NC2CCc3ccccc3N(CC(=O)O)C2=O,\"InChI=1S/C24H28N2O5/c1-2-31-24(30)20(14-12-17-8-4-3-5-9-17)25-19-15-13-18-10-6-7-11-21(18)26(23(19)29)16-22(27)28/h3-11,19-20,25H,2,12-16H2,1H3,(H,27,28)\",[C][C][O][C][=Branch1][C][=O][C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][Ring1][#C][=O],\"2-[3-[(1-ethoxy-1-oxo-4-phenylbutan-2-yl)amino]-2-oxo-4,5-dihydro-3h-1-benzazepin-1-yl]acetic acid\",-0.2\nCOc1ccc(Cl)c(Nc2ncnc3cc(OCC4CCN(C)CC4)c(OC)cc23)c1,\"InChI=1S/C23H27ClN4O3/c1-28-8-6-15(7-9-28)13-31-22-12-19-17(11-21(22)30-3)23(26-14-25-19)27-20-10-16(29-2)4-5-18(20)24/h4-5,10-12,14-15H,6-9,13H2,1-3H3,(H,25,26,27)\",[C][O][C][=C][C][=C][Branch1][C][Cl][C][Branch2][Ring2][Ring2][N][C][=N][C][=N][C][=C][C][Branch1][=C][O][C][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][Branch1][Ring1][O][C][C][=C][Ring2][Ring1][Branch1][Ring1][P][=C][Ring2][Ring1][=N],n-(2-chloro-5-methoxyphenyl)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinazolin-4-amine,2\nNc1ncc(nc1C(=O)Nc2cccnc2)c3ccc(cc3)S(=O)(=O)N4CCOCC4,\"InChI=1S/C20H20N6O4S/c21-19-18(20(27)24-15-2-1-7-22-12-15)25-17(13-23-19)14-3-5-16(6-4-14)31(28,29)26-8-10-30-11-9-26/h1-7,12-13H,8-11H2,(H2,21,23)(H,24,27)\",[N][C][=N][C][=C][Branch2][Ring1][C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1],3-amino-6-(4-morpholin-4-ylsulfonylphenyl)-n-pyridin-3-ylpyrazine-2-carboxamide,2.83\nCN1CCN(CC1)c2ccc(NC(=O)c3oc(Nc4ccccc4F)nn3)cn2,\"InChI=1S/C19H20FN7O2/c1-26-8-10-27(11-9-26)16-7-6-13(12-21-16)22-17(28)18-24-25-19(29-18)23-15-5-3-2-4-14(15)20/h2-7,12H,8-11H2,1H3,(H,22,28)(H,23,25)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][O][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][N][=Ring1][=N][C][=N][Ring2][Ring1][=Branch1],\"5-[(2-fluorophenyl)amino]-n-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]-1,3,4-oxadiazole-2-carboxamide\",2.36\nCOc1cc(N2CCN(C)CC2)c3nc(cc(N(C)C)c3c1)C(=O)Nc4ccc(cc4)N5CCOCC5,\"InChI=1S/C28H36N6O3/c1-31(2)25-19-24(28(35)29-20-5-7-21(8-6-20)33-13-15-37-16-14-33)30-27-23(25)17-22(36-4)18-26(27)34-11-9-32(3)10-12-34/h5-8,17-19H,9-16H2,1-4H3,(H,29,35)\",[C][O][C][=C][C][Branch1][N][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][N][=C][Branch1][P][C][=C][Branch1][=Branch1][N][Branch1][C][C][C][C][Ring1][=Branch2][=C][Ring2][Ring1][Ring2][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],4-dimethylamino-6-methoxy-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)quinoline-2-carboxamide,3.3\nCC1N(C(=O)c2ccccc2)c3ccccc3NC1=O,\"InChI=1S/C16H14N2O2/c1-11-15(19)17-13-9-5-6-10-14(13)18(11)16(20)12-7-3-2-4-8-12/h2-11H,1H3,(H,17,19)\",[C][C][N][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring2][Ring1][C][=O],\"4-(benzoyl)-3-methyl-1,3-dihydroquinoxalin-2-one\",2.11\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccccc2)NC(=O)OCC(F)(F)F)C(=O)C(F)(F)F,\"InChI=1S/C21H20F6N4O5/c1-11(2)15(16(33)21(25,26)27)30-14(32)9-31-17(12-6-4-3-5-7-12)28-8-13(18(31)34)29-19(35)36-10-20(22,23)24/h3-8,11,15H,9-10H2,1-2H3,(H,29,35)(H,30,32)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2,2,2-trifluoroethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-phenylpyrimidin-5-yl]carbamate\",2.37\nCOc1cc2ncnc(Nc3cc(NC(=O)c4ccnc(c4)N5CCOCC5)ccc3C)c2cc1OCCN6CCCC6,\"InChI=1S/C32H37N7O4/c1-22-5-6-24(36-32(40)23-7-8-33-30(17-23)39-12-14-42-15-13-39)18-26(22)37-31-25-19-29(43-16-11-38-9-3-4-10-38)28(41-2)20-27(25)34-21-35-31/h5-8,17-21H,3-4,9-16H2,1-2H3,(H,36,40)(H,34,35,37)\",[C][O][C][=C][C][=N][C][=N][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][=N][C][=C][Ring2][Ring1][P][O][C][C][N][C][C][C][C][Ring1][Branch1],n-[3-[[7-methoxy-6-(2-pyrrolidin-1-ylethoxy)quinazolin-4-yl]amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide,2.7\nNS(=O)(=O)c1cc2c(NC(Cc3ccccc3)NS2(=O)=O)cc1C(F)(F)F,\"InChI=1S/C15H14F3N3O4S2/c16-15(17,18)10-7-11-13(8-12(10)26(19,22)23)27(24,25)21-14(20-11)6-9-4-2-1-3-5-9/h1-5,7-8,14,20-21H,6H2,(H2,19,22,23)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch1][N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][Ring1][=N][=Branch1][C][=O][=O][C][=C][Ring2][Ring1][Ring1][C][Branch1][C][F][Branch1][C][F][F],\"1,1-dioxo-3-(phenylmethyl)-6-(trifluoromethyl)-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\",1.78\nC(CNCc1ccccc1)NCc2ccccc2,\"InChI=1S/C16H20N2/c1-3-7-15(8-4-1)13-17-11-12-18-14-16-9-5-2-6-10-16/h1-10,17-18H,11-14H2\",[C][Branch1][N][C][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n,n'-bis(phenylmethyl)ethane-1,2-diamine\",0.73\nCNCC[C@@H](Oc1ccc(cc1)C(F)(F)F)c2ccccc2,\"InChI=1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3/t16-/m1/s1\",[C][N][C][C][C@@H1][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1],(3r)-n-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine,1.96\nCc1cc(Oc2ccc3OCOc3c2)nc(Oc4ccc(cc4)n5ccnc5)n1,\"InChI=1S/C21H16N4O4/c1-14-10-20(28-17-6-7-18-19(11-17)27-13-26-18)24-21(23-14)29-16-4-2-15(3-5-16)25-9-8-22-12-25/h2-12H,13H2,1H3\",[C][C][=C][C][Branch1][#C][O][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][=N][C][Branch2][Ring1][Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1][=N][Ring2][Ring1][N],\"4-(1,3-benzodioxol-5-yloxy)-2-(4-imidazol-1-ylphenoxy)-6-methylpyrimidine\",3.47\nCOC(=O)CCCC(=O)Nc1ccc2C(=O)C(=O)c3ccccc3c2c1,\"InChI=1S/C20H17NO5/c1-26-18(23)8-4-7-17(22)21-12-9-10-15-16(11-12)13-5-2-3-6-14(13)19(24)20(15)25/h2-3,5-6,9-11H,4,7-8H2,1H3,(H,21,22)\",[C][O][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S],\"methyl 5-[(9,10-dioxophenanthren-3-yl)amino]-5-oxopentanoate\",2.96\nCCN(CC)S(=O)(=O)c1ccc(cc1)c2oc(SCC(=O)N3CCc4ccccc34)nn2,\"InChI=1S/C22H24N4O4S2/c1-3-25(4-2)32(28,29)18-11-9-17(10-12-18)21-23-24-22(30-21)31-15-20(27)26-14-13-16-7-5-6-8-19(16)26/h5-12H,3-4,13-15H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][O][C][Branch2][Ring1][Ring2][S][C][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][=N][N][=Ring2][Ring1][C],\"4-[5-[2-(2,3-dihydroindol-1-yl)-2-oxoethyl]sulfanyl-1,3,4-oxadiazol-2-yl]-n,n-diethylbenzenesulfonamide\",3.9\nOC(=O)C[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4sc(Cl)c(Cl)c4[nH]3,\"InChI=1S/C18H14Cl2N2O3S/c19-15-16-13(26-17(15)20)7-12(21-16)18(25)22-11-5-8-3-1-2-4-9(8)10(11)6-14(23)24/h1-4,7,10-11,21H,5-6H2,(H,22,25)(H,23,24)/t10-,11-/m1/s1\",[O][C][=Branch1][C][=O][C][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][S][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Ring1][#Branch1][NH1][Ring1][#Branch2],\"2-[(1r,2r)-2-[(2,3-dichloro4h-thieno[2,3-d]pyrrole-5-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]acetic acid\",2.53\nCN1CCN(CC1)c2cc(F)cc3C(=O)C=C(Nc23)C(=O)Nc4ccc(cc4)N5CCOCC5,\"InChI=1S/C25H28FN5O3/c1-29-6-8-31(9-7-29)22-15-17(26)14-20-23(32)16-21(28-24(20)22)25(33)27-18-2-4-19(5-3-18)30-10-12-34-13-11-30/h2-5,14-16H,6-13H2,1H3,(H,27,33)(H,28,32)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][N][C][Ring1][N][=Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],6-fluoro-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)-4-oxo-1h-quinoline-2-carboxamide,2.7\nCc1cc2cc(C)c3nnc(SCC(=O)N4CCN(CC4)C(=O)c5occc5)n3c2cc1C,\"InChI=1S/C24H25N5O3S/c1-15-11-18-12-17(3)22-25-26-24(29(22)19(18)13-16(15)2)33-14-21(30)27-6-8-28(9-7-27)23(31)20-5-4-10-32-20/h4-5,10-13H,6-9,14H2,1-3H3\",[C][C][=C][C][C][=C][Branch1][C][C][C][=N][N][=C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][N][Ring2][Ring1][=Branch1][C][=Ring2][Ring1][O][C][=C][Ring2][Ring1][#C][C],\"1-[4-(furan-2-carbonyl)piperazin-1-yl]-2-[(4,7,8-trimethyl-[1,2,4]triazolo[4,5-a]quinolin-1-yl)sulfanyl]ethanone\",2.8\nCN(C)CC(O)COc1ccc(Nc2cc(Nc3cc(C)ccc3Cl)ncn2)cc1,\"InChI=1S/C22H26ClN5O2/c1-15-4-9-19(23)20(10-15)27-22-11-21(24-14-25-22)26-16-5-7-18(8-6-16)30-13-17(29)12-28(2)3/h4-11,14,17,29H,12-13H2,1-3H3,(H2,24,25,26,27)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][Cl][=N][C][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1],1-[4-[[6-[(2-chloro-5-methylphenyl)amino]pyrimidin-4-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol,2.16\nCC(CN(C)C)CN1c2ccccc2CCc3ccccc13,\"InChI=1S/C20H26N2/c1-16(14-21(2)3)15-22-19-10-6-4-8-17(19)12-13-18-9-5-7-11-20(18)22/h4-11,16H,12-15H2,1-3H3\",[C][C][Branch1][#Branch1][C][N][Branch1][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n,n,2-trimethylpropan-1-amine\",2.95\nClc1ccc(NS(=O)(=O)c2ccc(Cl)s2)c(c1)C(=O)Nc3ccc(cc3)S(=O)(=O)N4CCOCC4,\"InChI=1S/C21H19Cl2N3O6S3/c22-14-1-6-18(25-34(28,29)20-8-7-19(23)33-20)17(13-14)21(27)24-15-2-4-16(5-3-15)35(30,31)26-9-11-32-12-10-26/h1-8,13,25H,9-12H2,(H,24,27)\",[Cl][C][=C][C][=C][Branch2][Ring1][Ring1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1][C][=Branch1][Ring2][=C][Ring1][S][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1],5-chloro-2-[(5-chlorothiophen-2-yl)sulfonylamino]-n-(4-morpholin-4-ylsulfonylphenyl)benzamide,3.02\nCCN1CCC[C@H]1CNC(=O)c2c(OC)ccc(Br)c2OC,\"InChI=1S/C16H23BrN2O3/c1-4-19-9-5-6-11(19)10-18-16(20)14-13(21-2)8-7-12(17)15(14)22-3/h7-8,11H,4-6,9-10H2,1-3H3,(H,18,20)/t11-/m0/s1\",[C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][Branch1][Ring1][O][C][C][=C][C][Branch1][C][Br][=C][Ring1][=Branch2][O][C],\"3-bromo-n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2,6-dimethoxybenzamide\",0.05\nOc1cc(ccc1NC(=O)Nc2ccccc2Br)[N+](=O)[O-],\"InChI=1S/C13H10BrN3O4/c14-9-3-1-2-4-10(9)15-13(19)16-11-6-5-8(17(20)21)7-12(11)18/h1-7,18H,(H2,15,16,19)\",[O][C][=C][C][=Branch2][Ring1][Branch1][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][Br][N+1][=Branch1][C][=O][O-1],3-(2-bromophenyl)-1-(2-hydroxy-4-nitrophenyl)urea,3.9\nCOc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C24H29Cl2N3O5S/c1-33-18-2-5-21(6-3-18)35(31,32)27-24(30)29-12-8-17(9-13-29)28-14-10-19(11-15-28)34-20-4-7-22(25)23(26)16-20/h2-7,16-17,19H,8-15H2,1H3,(H,27,30)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(4-methoxyphenyl)sulfonylpiperidine-1-carboxamide\",1.39\nClc1ccc(O[C@H]2CCCNC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C23H31ClN2O2/c24-21-4-3-18(28-19-2-1-5-25-13-19)9-20(21)22(27)26-14-23-10-15-6-16(11-23)8-17(7-15)12-23/h3-4,9,15-17,19,25H,1-2,5-8,10-14H2,(H,26,27)/t15?,16?,17?,19-,23?/m0/s1\",[Cl][C][=C][C][=C][Branch1][#Branch2][O][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chloro-5-[(3s)-piperidin-3-yl]oxybenzamide,2.18\nOc1ccc(cc1)C2=CC(=O)c3ccc(O)cc3O2,\"InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-8,16-17H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][Ring1][N],7-hydroxy-2-(4-hydroxyphenyl)chromen-4-one,3.2\nCc1cccc(Nc2ccccc2C(=O)O)c1C,\"InChI=1S/C15H15NO2/c1-10-6-5-9-13(11(10)2)16-14-8-4-3-7-12(14)15(17)18/h3-9,16H,1-2H3,(H,17,18)\",[C][C][=C][C][=C][C][Branch1][#C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][=C][Ring1][S][C],\"2-[(2,3-dimethylphenyl)amino]benzoic acid\",1.89\nCCCc1c(O)c(ccc1OCc2ccc(C(=O)O)c(Br)c2)C(=O)C,\"InChI=1S/C19H19BrO5/c1-3-4-15-17(8-7-13(11(2)21)18(15)22)25-10-12-5-6-14(19(23)24)16(20)9-12/h5-9,22H,3-4,10H2,1-2H3,(H,23,24)\",[C][C][C][C][=C][Branch1][C][O][C][=Branch2][Ring1][#Branch2][=C][C][=C][Ring1][#Branch1][O][C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][Br][=C][Ring1][#Branch2][C][=Branch1][C][=O][C],4-[(4-acetyl-3-hydroxy-2-propylphenoxy)methyl]-2-bromobenzoic acid,2.3\nCC1CCC(CC(=O)Nc2cccc3ncccc23)CC1,\"InChI=1S/C18H22N2O/c1-13-7-9-14(10-8-13)12-18(21)20-17-6-2-5-16-15(17)4-3-11-19-16/h2-6,11,13-14H,7-10,12H2,1H3,(H,20,21)\",[C][C][C][C][C][Branch2][Ring1][Branch1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=N][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][C][Ring2][Ring1][Ring2],2-(4-methylcyclohexyl)-n-quinolin-5-ylacetamide,3.56\nCCCN[C@H]1CCc2nc(N)sc2C1,\"InChI=1S/C10H17N3S/c1-2-5-12-7-3-4-8-9(6-7)14-10(11)13-8/h7,12H,2-6H2,1H3,(H2,11,13)/t7-/m0/s1\",[C][C][C][N][C@H1][C][C][C][N][=C][Branch1][C][N][S][C][=Ring1][=Branch1][C][Ring1][#Branch2],\"(6s)-n'-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine\",3.15\nNc1ccccc1NC(=O)c2ccc(cc2)c3ncc(CN4CCC4)cc3F,\"InChI=1S/C22H21FN4O/c23-18-12-15(14-27-10-3-11-27)13-25-21(18)16-6-8-17(9-7-16)22(28)26-20-5-2-1-4-19(20)24/h1-2,4-9,12-13H,3,10-11,14,24H2,(H,26,28)\",[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][Branch1][Branch2][C][N][C][C][C][Ring1][Ring2][C][=C][Ring1][O][F],n-(2-aminophenyl)-4-[5-(azetidin-1-ylmethyl)-3-fluoropyridin-2-yl]benzamide,1.69\nO[C@@H](CNCCCSCCNCCc1ccccc1Cl)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H28ClN3O3S2/c23-17-5-2-1-4-15(17)8-10-24-11-13-30-12-3-9-25-14-19(28)16-6-7-18(27)20-21(16)31-22(29)26-20/h1-2,4-7,19,24-25,27-28H,3,8-14H2,(H,26,29)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][Branch1][C][N][C][C][C][S][C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"7-[(1r)-2-[3-[2-[2-(2-chlorophenyl)ethylamino]ethylsulfanyl]propylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",0.99\nCc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1NC(=O)c3ccc4ncccc4c3,\"InChI=1S/C25H18F3N3O2/c1-15-7-9-20(30-23(32)17-4-2-6-19(13-17)25(26,27)28)14-22(15)31-24(33)18-8-10-21-16(12-18)5-3-11-29-21/h2-14H,1H3,(H,30,32)(H,31,33)\",[C][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring2][Ring1][Ring1][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],n-[2-methyl-5-[[3-(trifluoromethyl)benzoyl]amino]phenyl]quinoline-6-carboxamide,3.87\nc1ccc(cc1)c2nnc(s2)c3ccccc3,InChI=1S/C14H10N2S/c1-3-7-11(8-4-1)13-15-16-14(17-13)12-9-5-2-6-10-12/h1-10H,[C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2,5-di(phenyl)-1,3,4-thiadiazole\",4.2\nCC(C)(C)NCC(O)COc1nsnc1N2CCOCC2,\"InChI=1S/C13H24N4O3S/c1-13(2,3)14-8-10(18)9-20-12-11(15-21-16-12)17-4-6-19-7-5-17/h10,14,18H,4-9H2,1-3H3\",[C][C][Branch1][C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=N][S][N][=C][Ring1][Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"1-(tert-butylamino)-3-[(4-morpholin-4-yl-1,2,5-thiadiazol-3-yl)oxy]propan-2-ol\",-0.35\nCN1CCCC(CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1,\"InChI=1S/C18H26Cl2N4O/c1-22-6-2-3-14(12-22)13-23-7-9-24(10-8-23)18(25)21-15-4-5-16(19)17(20)11-15/h4-5,11,14H,2-3,6-10,12-13H2,1H3,(H,21,25)\",[C][N][C][C][C][C][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2],\"n-(3,4-dichlorophenyl)-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carboxamide\",1.98\nCCCCN(CCNC[C@H](O)c1ccc(O)c2NC(=O)Sc12)C(=O)CCOCCc3ccccc3,\"InChI=1S/C26H35N3O5S/c1-2-3-14-29(23(32)12-17-34-16-11-19-7-5-4-6-8-19)15-13-27-18-22(31)20-9-10-21(30)24-25(20)35-26(33)28-24/h4-10,22,27,30-31H,2-3,11-18H2,1H3,(H,28,33)/t22-/m0/s1\",[C][C][C][C][N][Branch2][Ring1][N][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1][C][=Branch1][C][=O][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-butyl-n-[2-[[(2r)-2-hydroxy-2-(4-hydroxy-2-oxo-3h-1,3-benzothiazol-7-yl)ethyl]amino]ethyl]-3-(2-phenylethoxy)propanamide\",2.51\nCc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)cc4,\"InChI=1S/C24H30ClN3O4S/c1-18-2-8-23(9-3-18)33(30,31)26-24(29)28-14-10-20(11-15-28)27-16-12-22(13-17-27)32-21-6-4-19(25)5-7-21/h2-9,20,22H,10-17H2,1H3,(H,26,29)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],4-[4-(4-chlorophenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide,1.6\nCc1cnc(cn1)C(=O)NCCc2ccc(cc2)S(=O)(=O)NC(=O)NC3CCCCC3,\"InChI=1S/C21H27N5O4S/c1-15-13-24-19(14-23-15)20(27)22-12-11-16-7-9-18(10-8-16)31(29,30)26-21(28)25-17-5-3-2-4-6-17/h7-10,13-14,17H,2-6,11-12H2,1H3,(H,22,27)(H2,25,26,28)\",[C][C][=C][N][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1],n-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-5-methylpyrazine-2-carboxamide,0.31\nOC(=O)c1ccccc1Cn2nnc(n2)c3cccc(OCc4ccc5ccccc5n4)c3,\"InChI=1S/C25H19N5O3/c31-25(32)22-10-3-1-7-19(22)15-30-28-24(27-29-30)18-8-5-9-21(14-18)33-16-20-13-12-17-6-2-4-11-23(17)26-20/h1-14H,15-16H2,(H,31,32)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][N][=N][C][=Branch1][Ring2][=N][Ring1][Branch1][C][=C][C][=C][C][Branch1][P][O][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][=C][Ring2][Ring1][C],2-[[5-[3-(quinolin-2-ylmethoxy)phenyl]tetrazol-2-yl]methyl]benzoic acid,2.1\nClc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)C3CC3,\"InChI=1S/C16H18ClNO2/c17-14-5-3-11(4-6-14)15(19)12-7-9-18(10-8-12)16(20)13-1-2-13/h3-6,12-13H,1-2,7-10H2\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][Ring1][Ring1],[4-(4-chlorobenzoyl)piperidin-1-yl]-cyclopropylmethanone,2.72\nO=C(Nc1cccc(NC(=O)c2ccccc2)n1)c3ccccc3,\"InChI=1S/C19H15N3O2/c23-18(14-8-3-1-4-9-14)21-16-12-7-13-17(20-16)22-19(24)15-10-5-2-6-11-15/h1-13H,(H2,20,21,22,23,24)\",[O][=C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][#C][C][=C][C][=C][C][=C][Ring1][=Branch1],n-[6-(benzoylamino)pyridin-2-yl]benzamide,4.02\nNc1ccc2ncccc2c1,\"InChI=1S/C9H8N2/c10-8-3-4-9-7(6-8)2-1-5-11-9/h1-6H,10H2\",[N][C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],quinolin-6-amine,1.33\nCc1c(Sc2ccc(Cl)cc2)c3c(Cl)nccc3n1CC(=O)O,\"InChI=1S/C16H12Cl2N2O2S/c1-9-15(23-11-4-2-10(17)3-5-11)14-12(6-7-19-16(14)18)20(9)8-13(21)22/h2-7H,8H2,1H3,(H,21,22)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][N][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],\"2-[4-chloro-3-(4-chlorophenyl)sulfanyl-2-methylpyrrolo[3,2-c]pyridin-1-yl]acetic acid\",0.92\nBrc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1,\"InChI=1S/C23H26BrN5O4/c24-15-1-3-19-18(11-15)29(22(31)14-33-19)10-9-28-7-5-16(6-8-28)25-12-17-2-4-20-23(26-17)27-21(30)13-32-20/h1-4,11,16,25H,5-10,12-14H2,(H,26,27,30)\",[Br][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S],\"6-[[[1-[2-(6-bromo-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",1.42\nCc1c(Oc2ccc(Cl)cc2)c3cc(ccc3n1CC(=O)O)C(F)(F)F,\"InChI=1S/C18H13ClF3NO3/c1-10-17(26-13-5-3-12(19)4-6-13)14-8-11(18(20,21)22)2-7-15(14)23(10)9-16(24)25/h2-8H,9H2,1H3,(H,24,25)\",[C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F],2-[3-(4-chlorophenoxy)-2-methyl-5-(trifluoromethyl)indol-1-yl]acetic acid,2.28\nCN(C)CCCN1c2ccccc2CCc3ccccc13,\"InChI=1S/C19H24N2/c1-20(2)14-7-15-21-18-10-5-3-8-16(18)12-13-17-9-4-6-11-19(17)21/h3-6,8-11H,7,12-15H2,1-2H3\",[C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n,n-dimethylpropan-1-amine\",2.49\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)CN3CCOCC3)C(=O)C(F)(F)F,\"InChI=1S/C25H29F3N4O5/c1-16(2)22(23(35)25(26,27)28)30-21(34)15-32-19(17-6-4-3-5-7-17)9-8-18(24(32)36)29-20(33)14-31-10-12-37-13-11-31/h3-9,16,22H,10-15H2,1-2H3,(H,29,33)(H,30,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-morpholin-4-yl-n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]acetamide\",2\nClc1cccc(c1)N2CCN(CCCN3N=C4C=CC=CN4C3=O)CC2,\"InChI=1S/C19H22ClN5O/c20-16-5-3-6-17(15-16)23-13-11-22(12-14-23)8-4-10-25-19(26)24-9-2-1-7-18(24)21-25/h1-3,5-7,9,15H,4,8,10-14H2\",[Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][N][Branch2][Ring1][C][C][C][C][N][N][=C][C][=C][C][=C][N][Ring1][=Branch1][C][Ring1][=Branch2][=O][C][C][Ring2][Ring1][Ring1],\"2-[3-[4-(3-chlorophenyl)piperazin-1-yl]propyl]-[1,2,4]triazolo[4,5-a]pyridin-3-one\",2.67\nCC(C)NCC(O)COc1ccccc1OCC=C,\"InChI=1S/C15H23NO3/c1-4-9-18-14-7-5-6-8-15(14)19-11-13(17)10-16-12(2)3/h4-8,12-13,16-17H,1,9-11H2,2-3H3\",[C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=C],1-(propan-2-ylamino)-3-(2-prop-2-enoxyphenoxy)propan-2-ol,0.2\nO=C(N1CCCCC1)c2scc3CCCCc23,\"InChI=1S/C14H19NOS/c16-14(15-8-4-1-5-9-15)13-12-7-3-2-6-11(12)10-17-13/h10H,1-9H2\",[O][=C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1][C][S][C][=C][C][C][C][C][C][=Ring1][=Branch2][Ring1][=Branch1],\"piperidin-1-yl-(4,5,6,7-tetrahydro-2-benzothiophen-1-yl)methanone\",3.16\nNC(=O)Nc1sc(cc1C(=O)N)c2ccc(OCCN3CCCCC3)cc2,\"InChI=1S/C19H24N4O3S/c20-17(24)15-12-16(27-18(15)22-19(21)25)13-4-6-14(7-5-13)26-11-10-23-8-2-1-3-9-23/h4-7,12H,1-3,8-11H2,(H2,20,24)(H3,21,22,25)\",[N][C][=Branch1][C][=O][N][C][S][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][N][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][#C],2-(carbamoylamino)-5-[4-(2-piperidin-1-ylethoxy)phenyl]thiophene-3-carboxamide,1.2\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccs2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C24H23F3N4O5S/c1-14(2)19(20(33)24(25,26)27)30-18(32)12-31-21(17-9-6-10-37-17)28-11-16(22(31)34)29-23(35)36-13-15-7-4-3-5-8-15/h3-11,14,19H,12-13H2,1-2H3,(H,29,35)(H,30,32)\",[C][C][Branch1][C][C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=N][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-thiophen-2-ylpyrimidin-5-yl]carbamate\",2.02\nOc1ccc(cc1)C2CNCCc3c(Cl)c(O)c(O)cc23,\"InChI=1S/C16H16ClNO3/c17-15-11-5-6-18-8-13(9-1-3-10(19)4-2-9)12(11)7-14(20)16(15)21/h1-4,7,13,18-21H,5-6,8H2\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][C][N][C][C][C][=C][Branch1][C][Cl][C][Branch1][C][O][=C][Branch1][C][O][C][=C][Ring1][=C][Ring1][=Branch2],\"6-chloro-1-(4-hydroxyphenyl)-2,3,4,5-tetrahydro-1h-3-benzazepine-7,8-diol\",0.87\nCC(C)n1c(C)ncc1c2ccnc(Nc3ccccc3)n2,\"InChI=1S/C17H19N5/c1-12(2)22-13(3)19-11-16(22)15-9-10-18-17(21-15)20-14-7-5-4-6-8-14/h4-12H,1-3H3,(H,18,20,21)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N],4-(2-methyl-3-propan-2-ylimidazol-4-yl)-n-phenylpyrimidin-2-amine,3.58\n[O-]c1c2c(nn1c3ccc(Cl)cc3)c4ccccc4c[n+]2Cc5ccccc5,\"InChI=1S/C23H16ClN3O/c24-18-10-12-19(13-11-18)27-23(28)22-21(25-27)20-9-5-4-8-17(20)15-26(22)14-16-6-2-1-3-7-16/h1-13,15H,14H2\",[O-1][C][=C][C][=Branch1][S][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N+1][Ring2][Ring1][Ring1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-(4-chlorophenyl)-4-(phenylmethyl)pyrazolo[4,5-c]isoquinolin-4-ium-3-olate\",4.5\nCOc1ccc(CNC(=O)Nc2ncc(s2)[N+](=O)[O-])cc1,\"InChI=1S/C12H12N4O4S/c1-20-9-4-2-8(3-5-9)6-13-11(17)15-12-14-7-10(21-12)16(18)19/h2-5,7H,6H2,1H3,(H2,13,14,15,17)\",[C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][C][N][C][=Branch1][C][=O][N][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][N+1][=Branch1][C][=O][O-1][C][=C][Ring2][Ring1][Ring1],\"1-[(4-methoxyphenyl)methyl]-3-(5-nitro-1,3-thiazol-2-yl)urea\",2.9\nOc1cc(O)c2C(=O)C(=COc2c1)c3ccc(O)c(O)c3,\"InChI=1S/C15H10O6/c16-8-4-12(19)14-13(5-8)21-6-9(15(14)20)7-1-2-10(17)11(18)3-7/h1-6,16-19H\",[O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2],\"3-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one\",2.45\nCOc1ccc(cc1)C2=C(C)c3ccc(OC)cc3OC2=O,\"InChI=1S/C18H16O4/c1-11-15-9-8-14(21-3)10-16(15)22-18(19)17(11)12-4-6-13(20-2)7-5-12/h4-10H,1-3H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][Branch1][C][C][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][O][C][Ring1][=N][=O],7-methoxy-3-(4-methoxyphenyl)-4-methylchromen-2-one,3.31\nCC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)\\C(=N/OCOCCOC)\\[C@H](C)[C@@H](O)[C@]1(C)O,\"InChI=1S/C41H76N2O15/c1-15-29-41(10,49)34(45)24(4)31(42-53-21-52-17-16-50-13)22(2)19-39(8,48)36(58-38-32(44)28(43(11)12)18-23(3)54-38)25(5)33(26(6)37(47)56-29)57-30-20-40(9,51-14)35(46)27(7)55-30/h22-30,32-36,38,44-46,48-49H,15-21H2,1-14H3/b42-31+/t22-,23-,24+,25+,26-,27+,28+,29-,30+,32-,33+,34-,35+,36-,38+,39-,40-,41-/m1/s1\",[C][C][C@H1][O][C][=Branch1][C][=O][C@H1][Branch1][C][C][C@@H1][Branch2][Ring1][#Branch1][O][C@H1][C][C@@][Branch1][C][C][Branch1][Ring1][O][C][C@@H1][Branch1][C][O][C@H1][Branch1][C][C][O][Ring1][O][C@H1][Branch1][C][C][C@@H1][Branch2][Ring1][Branch1][O][C@@H1][O][C@H1][Branch1][C][C][C][C@@H1][Branch1][Branch1][C@H1][Ring1][#Branch1][O][N][Branch1][C][C][C][C@][Branch1][C][C][Branch1][C][O][C][C@@H1][Branch1][C][C][\\C][=Branch1][=Branch2][=N][/O][C][O][C][C][O][C][\\C@H1][Branch1][C][C][C@@H1][Branch1][C][O][C@][Ring2][Branch1][=Branch1][Branch1][C][C][O],\"(3r,4s,5s,6r,7r,9r,10e,11s,12r,13s,14r)-6-[(2s,3r,4s,6r)-4-dimethylamino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2r,4r,5s,6s)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-(2-methoxyethoxymethoxyimino)-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecan-2-one\",1.8\nCOc1cc2ncc(C(=O)N)c(Nc3ccc(F)cc3F)c2cc1OC,\"InChI=1S/C18H15F2N3O3/c1-25-15-6-10-14(7-16(15)26-2)22-8-11(18(21)24)17(10)23-13-4-3-9(19)5-12(13)20/h3-8H,1-2H3,(H2,21,24)(H,22,23)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C],\"4-[(2,4-difluorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",2.95\nCc1ccc(O)c(O)c1,\"InChI=1S/C7H8O2/c1-5-2-3-6(8)7(9)4-5/h2-4,8-9H,1H3\",[C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2],\"4-methylbenzene-1,2-diol\",1.37\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1NC(=O)\\C=C\\CN4CCCCC4,\"InChI=1S/C24H25ClFN5O2/c1-33-22-14-20-17(24(28-15-27-20)29-16-7-8-19(26)18(25)12-16)13-21(22)30-23(32)6-5-11-31-9-3-2-4-10-31/h5-8,12-15H,2-4,9-11H2,1H3,(H,30,32)(H,27,28,29)/b6-5+\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][N][C][=Branch1][C][=O][\\C][=C][\\C][N][C][C][C][C][C][Ring1][=Branch1],(e)-n-[4-[(3-chloro-4-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]-4-piperidin-1-ylbut-2-enamide,4.1\nCc1ncc(CO)c(CO)c1O,\"InChI=1S/C8H11NO3/c1-5-8(12)7(4-11)6(3-10)2-9-5/h2,10-12H,3-4H2,1H3\",[C][C][=N][C][=C][Branch1][Ring1][C][O][C][Branch1][Ring1][C][O][=C][Ring1][#Branch2][O],\"4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol\",-0.58\nCCCSc1nc2ccc(NC(=O)CCC(=O)O)cc2s1,\"InChI=1S/C14H16N2O3S2/c1-2-7-20-14-16-10-4-3-9(8-11(10)21-14)15-12(17)5-6-13(18)19/h3-4,8H,2,5-7H2,1H3,(H,15,17)(H,18,19)\",[C][C][C][S][C][=N][C][=C][C][=C][Branch1][=N][N][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][O][C][=C][Ring1][=C][S][Ring1][P],\"4-oxo-4-[(2-propylsulfanyl-1,3-benzothiazol-6-yl)amino]butanoic acid\",0.5\nFc1cc(F)cc(c1)c2cc(on2)N(CCCN3CCCCCC3)Cc4ccc5OCOc5c4,\"InChI=1S/C26H29F2N3O3/c27-21-13-20(14-22(28)15-21)23-16-26(34-29-23)31(11-5-10-30-8-3-1-2-4-9-30)17-19-6-7-24-25(12-19)33-18-32-24/h6-7,12-16H,1-5,8-11,17-18H2\",[F][C][=C][C][Branch1][C][F][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][C][=C][Branch1][Branch1][O][N][=Ring1][Branch1][N][Branch1][=N][C][C][C][N][C][C][C][C][C][C][Ring1][#Branch1][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2],\"n-[3-(azepan-1-yl)propyl]-n-(1,3-benzodioxol-5-ylmethyl)-3-(3,5-difluorophenyl)-1,2-oxazol-5-amine\",3.84\nCC(C)c1ccccc1Nc2nc(SCc3cccs3)n[nH]2,\"InChI=1S/C16H18N4S2/c1-11(2)13-7-3-4-8-14(13)17-15-18-16(20-19-15)22-10-12-6-5-9-21-12/h3-9,11H,10H2,1-2H3,(H2,17,18,19,20)\",[C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=N][C][Branch1][#Branch2][S][C][C][=C][C][=C][S][Ring1][Branch1][=N][NH1][Ring1][N],\"n-(2-propan-2-ylphenyl)-5-(thiophen-2-ylmethylsulfanyl)-2h-1,2,4-triazol-3-amine\",4.21\nNc1nc2ccc(F)cc2s1,\"InChI=1S/C7H5FN2S/c8-4-1-2-5-6(3-4)11-7(9)10-5/h1-3H,(H2,9,10)\",[N][C][=N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][S][Ring1][#Branch2],\"6-fluoro-1,3-benzothiazol-2-amine\",2.2\nOc1ccc(cc1)S(=O)(=O)Nc2nccs2,\"InChI=1S/C9H8N2O3S2/c12-7-1-3-8(4-2-7)16(13,14)11-9-10-5-6-15-9/h1-6,12H,(H,10,11)\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"4-hydroxy-n-(1,3-thiazol-2-yl)benzenesulfonamide\",0.36\nClc1cccc(Nc2ncnc3ccccc23)c1,\"InChI=1S/C14H10ClN3/c15-10-4-3-5-11(8-10)18-14-12-6-1-2-7-13(12)16-9-17-14/h1-9H,(H,16,17,18)\",[Cl][C][=C][C][=C][C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][P],n-(3-chlorophenyl)quinazolin-4-amine,3.9\nO=C(NC1CCCC1)C(N(Cc2occc2)C(=O)c3ccc([nH]3)c4ccccc4)c5ccncc5,\"InChI=1S/C28H28N4O3/c33-27(30-22-9-4-5-10-22)26(21-14-16-29-17-15-21)32(19-23-11-6-18-35-23)28(34)25-13-12-24(31-25)20-7-2-1-3-8-20/h1-3,6-8,11-18,22,26,31H,4-5,9-10,19H2,(H,30,33)\",[O][=C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][Branch1][C][Branch2][Ring1][P][N][Branch1][=Branch2][C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1],n-[2-(cyclopentylamino)-2-oxo-1-pyridin-4-ylethyl]-n-(furan-2-ylmethyl)-5-phenyl-1h-pyrrole-2-carboxamide,4.36\nCN1C(=N)N(CC(=O)c2ccc(Cl)cc2)c3ccccc13,\"InChI=1S/C16H14ClN3O/c1-19-13-4-2-3-5-14(13)20(16(19)18)10-15(21)11-6-8-12(17)9-7-11/h2-9,18H,10H2,1H3\",[C][N][C][=Branch1][C][=N][N][Branch1][P][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][Ring2][Ring1][=Branch1],1-(4-chlorophenyl)-2-(2-imino-3-methylbenzimidazol-1-yl)ethanone,1.63\nCN1CCN(CC1)C(=O)c2cc3cc(Br)ccc3[nH]2,\"InChI=1S/C14H16BrN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Br][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],(5-bromo-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone,2.79\nCOc1cccc(c1)C(=O)N2CCC(CC2)N3C(=O)Nc4ccccc34,\"InChI=1S/C20H21N3O3/c1-26-16-6-4-5-14(13-16)19(24)22-11-9-15(10-12-22)23-18-8-3-2-7-17(18)21-20(23)25/h2-8,13,15H,9-12H2,1H3,(H,21,25)\",[C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],3-[1-(3-methoxybenzoyl)piperidin-4-yl]-1h-benzimidazol-2-one,2.65\nCCCS(=O)(=O)N1CCCC(C1)C(=O)N2CCC(Cc3ccccc3)CC2,\"InChI=1S/C21H32N2O3S/c1-2-15-27(25,26)23-12-6-9-20(17-23)21(24)22-13-10-19(11-14-22)16-18-7-4-3-5-8-18/h3-5,7-8,19-20H,2,6,9-17H2,1H3\",[C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring1][=N],[4-(phenylmethyl)piperidin-1-yl]-(1-propylsulfonylpiperidin-3-yl)methanone,3.44\nCN1CCCC1c2cccnc2,\"InChI=1S/C10H14N2/c1-12-7-3-5-10(12)9-4-2-6-11-8-9/h2,4,6,8,10H,3,5,7H2,1H3\",[C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],3-(1-methylpyrrolidin-2-yl)pyridine,0.5\nCN(C)c1cccc2c(cccc12)S(=O)(=O)Nc3cnccn3,\"InChI=1S/C16H16N4O2S/c1-20(2)14-7-3-6-13-12(14)5-4-8-15(13)23(21,22)19-16-11-17-9-10-18-16/h3-11H,1-2H3,(H,18,19)\",[C][N][Branch1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][N][=C][C][=N][Ring1][=Branch1],5-dimethylamino-n-pyrazin-2-ylnaphthalene-1-sulfonamide,0.9\nOc1ccc(cc1)C2CC(=O)c3ccc(O)cc3O2,\"InChI=1S/C15H12O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-7,14,16-17H,8H2\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][Ring1][N],7-hydroxy-2-(4-hydroxyphenyl)chroman-4-one,2.4\nNCc1nc2ccccc2[nH]1,\"InChI=1S/C8H9N3/c9-5-8-10-6-3-1-2-4-7(6)11-8/h1-4H,5,9H2,(H,10,11)\",[N][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],1h-benzimidazol-2-ylmethanamine,0.4\nOC(=O)c1cc(nc2ccc(F)cc12)c3ccncc3,\"InChI=1S/C15H9FN2O2/c16-10-1-2-13-11(7-10)12(15(19)20)8-14(18-13)9-3-5-17-6-4-9/h1-8H,(H,19,20)\",[O][C][=Branch1][C][=O][C][=C][C][=Branch1][#C][=N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][O][Ring1][#Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1],6-fluoro-2-pyridin-4-ylquinoline-4-carboxylic acid,-0.8\nNc1nccc(n1)c2ccccc2,\"InChI=1S/C10H9N3/c11-10-12-7-6-9(13-10)8-4-2-1-3-5-8/h1-7H,(H2,11,12,13)\",[N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],4-phenylpyrimidin-2-amine,2\nCC(CCc1cccc(OCc2ccc3ccccc3n2)c1)CC(=O)O,\"InChI=1S/C22H23NO3/c1-16(13-22(24)25)9-10-17-5-4-7-20(14-17)26-15-19-12-11-18-6-2-3-8-21(18)23-19/h2-8,11-12,14,16H,9-10,13,15H2,1H3,(H,24,25)\",[C][C][Branch2][Ring1][=C][C][C][C][=C][C][=C][C][Branch1][P][O][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][=C][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],3-methyl-5-[3-(quinolin-2-ylmethoxy)phenyl]pentanoic acid,2.4\nCCCc1c(OCCCSc2ccc(CC(=O)O)cc2Cl)ccc3c(CC)noc13,\"InChI=1S/C23H26ClNO4S/c1-3-6-17-20(9-8-16-19(4-2)25-29-23(16)17)28-11-5-12-30-21-10-7-15(13-18(21)24)14-22(26)27/h7-10,13H,3-6,11-12,14H2,1-2H3,(H,26,27)\",[C][C][C][C][=C][Branch2][Ring1][#Branch1][O][C][C][C][S][C][=C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][Ring1][#Branch2][Cl][C][=C][C][C][Branch1][Ring1][C][C][=N][O][C][Ring2][Ring1][O][=Ring1][#Branch1],\"2-[3-chloro-4-[3-[(3-ethyl-7-propyl-1,2-benzoxazol-6-yl)oxy]propylsulfanyl]phenyl]acetic acid\",3.92\nOC(=O)c1cc(ccc1O)c2ccc(F)cc2F,\"InChI=1S/C13H8F2O3/c14-8-2-3-9(11(15)6-8)7-1-4-12(16)10(5-7)13(17)18/h1-6,16H,(H,17,18)\",[O][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F],\"5-(2,4-difluorophenyl)-2-hydroxybenzoic acid\",0.59\nO[C@@H](CNCCSCCCNCCc1cccc(c1)C(F)(F)F)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C23H28F3N3O3S2/c24-23(25,26)16-4-1-3-15(13-16)7-9-27-8-2-11-33-12-10-28-14-19(31)17-5-6-18(30)20-21(17)34-22(32)29-20/h1,3-6,13,19,27-28,30-31H,2,7-12,14H2,(H,29,32)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][=C][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[2-[3-(trifluoromethyl)phenyl]ethylamino]propylsulfanyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\",1.21\nCc1c(Sc2ccc(Cl)cc2)c3cc(Cl)ccc3n1CC(=O)O,\"InChI=1S/C17H13Cl2NO2S/c1-10-17(23-13-5-2-11(18)3-6-13)14-8-12(19)4-7-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],2-[5-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid,2.87\nCN1[C@@H]2CC[C@H]1C[C@H](C2)OC(c3ccccc3)c4ccccc4,\"InChI=1S/C21H25NO/c1-22-18-12-13-19(22)15-20(14-18)23-21(16-8-4-2-5-9-16)17-10-6-3-7-11-17/h2-11,18-21H,12-15H2,1H3/t18-,19+,20+\",[C][N][C@@H1][C][C][C@H1][Ring1][Branch1][C][C@H1][Branch1][Ring2][C][Ring1][#Branch1][O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(1r,5s)-3-[di(phenyl)methoxy]-8-methyl-8-azabicyclo[3.2.1]octane\",1.49\nOc1cccc(c1)N2C(=O)c3ccc(O)cc3C2=O,\"InChI=1S/C14H9NO4/c16-9-3-1-2-8(6-9)15-13(18)11-5-4-10(17)7-12(11)14(15)19/h1-7,16-17H\",[O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Ring1][O][=O],\"5-hydroxy-2-(3-hydroxyphenyl)isoindole-1,3-dione\",2\nNS(=O)(=O)c1ccc(NCc2ccccc2)cc1,\"InChI=1S/C13H14N2O2S/c14-18(16,17)13-8-6-12(7-9-13)15-10-11-4-2-1-3-5-11/h1-9,15H,10H2,(H2,14,16,17)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=C],4-(phenylmethylamino)benzenesulfonamide,1.7\nFC(F)(F)COc1ccc(OCC(F)(F)F)c(c1)C(=O)NCC2CCCCN2,\"InChI=1S/C17H20F6N2O3/c18-16(19,20)9-27-12-4-5-14(28-10-17(21,22)23)13(7-12)15(26)25-8-11-3-1-2-6-24-11/h4-5,7,11,24H,1-3,6,8-10H2,(H,25,26)\",[F][C][Branch1][C][F][Branch1][C][F][C][O][C][=C][C][=C][Branch1][O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][Ring2][=C][Ring1][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][N][Ring1][=Branch1],\"n-(piperidin-2-ylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide\",1.13\nCOc1ccc(cc1F)c2cc(nn2c3ccc(cc3)S(=O)(=O)N)C(F)F,\"InChI=1S/C17H14F3N3O3S/c1-26-16-7-2-10(8-13(16)18)15-9-14(17(19)20)22-23(15)11-3-5-12(6-4-11)27(21,24)25/h2-9,17H,1H3,(H2,21,24,25)\",[C][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][C][=C][C][=Branch2][Ring1][#Branch1][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][F][F],4-[3-(difluoromethyl)-5-(3-fluoro-4-methoxyphenyl)pyrazol-1-yl]benzenesulfonamide,2.8\nC(N(Cc1ccccc1)c2nn[nH]n2)c3ccccc3,\"InChI=1S/C15H15N5/c1-3-7-13(8-4-1)11-20(15-16-18-19-17-15)12-14-9-5-2-6-10-14/h1-10H,11-12H2,(H,16,17,18,19)\",[C][Branch2][Ring1][Ring2][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][=N][NH1][N][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n,n-bis(phenylmethyl)-2h-tetrazol-5-amine\",1.37\nCN1CCN(CC1)c2nc(CCOc3ccc(C[C@H](Nc4ccccc4C(=O)c5ccccc5)C(=O)O)cc3)c(C)s2,\"InChI=1S/C33H36N4O4S/c1-23-28(35-33(42-23)37-19-17-36(2)18-20-37)16-21-41-26-14-12-24(13-15-26)22-30(32(39)40)34-29-11-7-6-10-27(29)31(38)25-8-4-3-5-9-25/h3-15,30,34H,16-22H2,1-2H3,(H,39,40)/t30-/m0/s1\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][Branch2][Ring2][#C][C][C][O][C][=C][C][=C][Branch2][Ring1][S][C][C@H1][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][#Branch2][=C][Branch1][C][C][S][Ring2][Ring2][Ring1],\"(2s)-2-[[2-(benzoyl)phenyl]amino]-3-[4-[2-[5-methyl-2-(4-methylpiperazin-1-yl)-1,3-thiazol-4-yl]ethoxy]phenyl]propanoic acid\",2.58\nC[C@H]1CN(Cc2cc(Cl)ccc2CCC(=O)O)CCN1C(=O)Cc3ccccc3,\"InChI=1S/C23H27ClN2O3/c1-17-15-25(11-12-26(17)22(27)13-18-5-3-2-4-6-18)16-20-14-21(24)9-7-19(20)8-10-23(28)29/h2-7,9,14,17H,8,10-13,15-16H2,1H3,(H,28,29)/t17-/m0/s1\",[C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],3-[4-chloro-2-[[(3s)-3-methyl-4-(2-phenylacetyl)piperazin-1-yl]methyl]phenyl]propanoic acid,1.52\nNc1ccc2c3ccccc3C(=O)C(=O)c2c1,\"InChI=1S/C14H9NO2/c15-8-5-6-10-9-3-1-2-4-11(9)13(16)14(17)12(10)7-8/h1-7H,15H2\",[N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][Ring1][N][=C][Ring1][S],\"2-aminophenanthrene-9,10-dione\",2.23\nCOc1ccc(N(C(C(=O)NC2CCCC2)c3ccccc3F)C(=O)c4occc4)c(OC)c1,\"InChI=1S/C26H27FN2O5/c1-32-18-13-14-21(23(16-18)33-2)29(26(31)22-12-7-15-34-22)24(19-10-5-6-11-20(19)27)25(30)28-17-8-3-4-9-17/h5-7,10-17,24H,3-4,8-9H2,1-2H3,(H,28,30)\",[C][O][C][=C][C][=C][Branch2][Ring2][Branch2][N][Branch2][Ring1][=Branch2][C][Branch1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][S],\"n-[2-(cyclopentylamino)-1-(2-fluorophenyl)-2-oxoethyl]-n-(2,4-dimethoxyphenyl)furan-2-carboxamide\",3.09\nC[C@H](C1=CNC(=S)N1)c2cccc(C)c2C,\"InChI=1S/C13H16N2S/c1-8-5-4-6-11(9(8)2)10(3)12-7-14-13(16)15-12/h4-7,10H,1-3H3,(H2,14,15,16)/t10-/m0/s1\",[C][C@H1][Branch1][O][C][=C][N][C][=Branch1][C][=S][N][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C],\"4-[(1s)-1-(2,3-dimethylphenyl)ethyl]-1,3-dihydroimidazole-2-thione\",2.9\nCN(C)CCOc1cc(NS(=O)(=O)c2c(Cl)cc(cc2Cl)C(F)(F)F)ccc1Cl,\"InChI=1S/C17H16Cl3F3N2O3S/c1-25(2)5-6-28-15-9-11(3-4-12(15)18)24-29(26,27)16-13(19)7-10(8-14(16)20)17(21,22)23/h3-4,7-9,24H,5-6H2,1-2H3\",[C][N][Branch1][C][C][C][C][O][C][=C][C][Branch2][Ring1][#C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][Branch1][=Branch1][C][=C][Ring1][#Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F][=C][C][=C][Ring2][Ring1][=Branch1][Cl],\"2,6-dichloro-n-[4-chloro-3-(2-dimethylaminoethoxy)phenyl]-4-(trifluoromethyl)benzenesulfonamide\",2.99\nOc1ccc(cc1)C2=Cc3ccc(O)cc3OC2=O,\"InChI=1S/C15H10O4/c16-11-4-1-9(2-5-11)13-7-10-3-6-12(17)8-14(10)19-15(13)18/h1-8,16-17H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O],7-hydroxy-3-(4-hydroxyphenyl)chromen-2-one,2.9\nCOc1cc(C)c(c(C)c1)S(=O)(=O)N(C)CCOCC(=O)N2CCN(CC2)C3CCN(C)CC3,\"InChI=1S/C24H40N4O5S/c1-19-16-22(32-5)17-20(2)24(19)34(30,31)26(4)14-15-33-18-23(29)28-12-10-27(11-13-28)21-6-8-25(3)9-7-21/h16-17,21H,6-15,18H2,1-5H3\",[C][O][C][=C][C][Branch1][C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][Branch1][C][C][C][C][O][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],\"4-methoxy-n,2,6-trimethyl-n-[2-[2-[4-(1-methylpiperidin-4-yl)piperazin-1-yl]-2-oxoethoxy]ethyl]benzenesulfonamide\",-0.4\nNc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C18H23ClN2O/c19-16-2-1-14(20)6-15(16)17(22)21-10-18-7-11-3-12(8-18)5-13(4-11)9-18/h1-2,6,11-13H,3-5,7-10,20H2,(H,21,22)\",[N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-5-amino-2-chlorobenzamide,3.45\nCCCCSc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1,\"InChI=1S/C14H21N5O4S/c1-2-3-4-24-14-17-11(15)8-12(18-14)19(6-16-8)13-10(22)9(21)7(5-20)23-13/h6-7,9-10,13,20-22H,2-5H2,1H3,(H2,15,17,18)/t7-,9-,10-,13-/m1/s1\",[C][C][C][C][S][C][=N][C][Branch1][C][N][=C][N][=C][N][Branch1][S][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O][C][Ring1][=C][=N][Ring2][Ring1][Ring1],\"(2r,3r,4s,5r)-2-(6-amino-2-butylsulfanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol\",1.51\nOc1ccc(cc1)c2ccc3cc(O)ccc3c2,\"InChI=1S/C16H12O2/c17-15-6-3-11(4-7-15)12-1-2-14-10-16(18)8-5-13(14)9-12/h1-10,17-18H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][C][Ring1][#Branch1][=C][Ring1][O],6-(4-hydroxyphenyl)naphthalen-2-ol,4\nNC(=O)C1=CN(Cc2ccc(F)c(F)c2)C(=O)C=C1,\"InChI=1S/C13H10F2N2O2/c14-10-3-1-8(5-11(10)15)6-17-7-9(13(16)19)2-4-12(17)18/h1-5,7H,6H2,(H2,16,19)\",[N][C][=Branch1][C][=O][C][=C][N][Branch1][S][C][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2][C][=Branch1][C][=O][C][=C][Ring1][S],\"1-[(3,4-difluorophenyl)methyl]-6-oxopyridine-3-carboxamide\",1.37\nOC(=O)c1ccc(cc1)c2ccc(Cl)c(c2)C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C25H26ClNO3/c26-22-6-5-20(18-1-3-19(4-2-18)24(29)30)10-21(22)23(28)27-14-25-11-15-7-16(12-25)9-17(8-15)13-25/h1-6,10,15-17H,7-9,11-14H2,(H,27,28)(H,29,30)\",[O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],4-[3-(1-adamantylmethylcarbamoyl)-4-chlorophenyl]benzoic acid,2.48\nCOc1cc2c(Nc3ncc(CC(=O)Nc4cccc(F)c4)s3)ncnc2cc1OCCCN5CCC(CO)CC5,\"InChI=1S/C29H33FN6O4S/c1-39-25-14-23-24(15-26(25)40-11-3-8-36-9-6-19(17-37)7-10-36)32-18-33-28(23)35-29-31-16-22(41-29)13-27(38)34-21-5-2-4-20(30)12-21/h2,4-5,12,14-16,18-19,37H,3,6-11,13,17H2,1H3,(H,34,38)(H,31,32,33,35)\",[C][O][C][=C][C][=C][Branch2][Ring1][=N][N][C][=N][C][=C][Branch2][Ring1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][S][Ring1][S][N][=C][N][=C][Ring2][Ring1][#Branch1][C][=C][Ring2][Ring1][O][O][C][C][C][N][C][C][C][Branch1][Ring1][C][O][C][C][Ring1][Branch2],\"n-(3-fluorophenyl)-2-[2-[[7-[3-[4-(hydroxymethyl)piperidin-1-yl]propoxy]-6-methoxyquinazolin-4-yl]amino]-1,3-thiazol-5-yl]acetamide\",2.89\nCCCCN(CCCC)CCCOC(=O)c1ccc(N)cc1,\"InChI=1S/C18H30N2O2/c1-3-5-12-20(13-6-4-2)14-7-15-22-18(21)16-8-10-17(19)11-9-16/h8-11H,3-7,12-15,19H2,1-2H3\",[C][C][C][C][N][Branch1][Branch1][C][C][C][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],3-(dibutylamino)propyl 4-aminobenzoate,1.93\nOC(=O)C(N1CCC(CN2CCC(CC2)Oc3ccc(Cl)c(Cl)c3)CC1)c4ccccc4,\"InChI=1S/C25H30Cl2N2O3/c26-22-7-6-21(16-23(22)27)32-20-10-12-28(13-11-20)17-18-8-14-29(15-9-18)24(25(30)31)19-4-2-1-3-5-19/h1-7,16,18,20,24H,8-15,17H2,(H,30,31)\",[O][C][=Branch1][C][=O][C][Branch2][Ring2][#Branch1][N][C][C][C][Branch2][Ring1][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][C][Ring2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[4-[[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl]piperidin-1-yl]-2-phenylacetic acid\",2.17\nCN(C)S(=O)(=O)c1ccc2Sc3ccccc3\\C(=C\\CCN4CCN(C)CC4)\\c2c1,\"InChI=1S/C23H29N3O2S2/c1-24(2)30(27,28)18-10-11-23-21(17-18)19(20-7-4-5-9-22(20)29-23)8-6-12-26-15-13-25(3)14-16-26/h4-5,7-11,17H,6,12-16H2,1-3H3/b19-8-\",[C][N][Branch1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][\\C][=Branch1][#C][=C][\\C][C][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][\\C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2],\"(9z)-n,n-dimethyl-9-[3-(4-methylpiperazin-1-yl)propylidene]thioxanthene-2-sulfonamide\",3.16\nOc1c(I)cc(I)c2cccnc12,\"InChI=1S/C9H5I2NO/c10-6-4-7(11)9(13)8-5(6)2-1-3-12-8/h1-4,13H\",[O][C][=C][Branch1][C][I][C][=C][Branch1][C][I][C][=C][C][=C][N][=C][Ring1][N][Ring1][=Branch1],\"5,7-diiodoquinolin-8-ol\",2.19\nCN[C@H]1CC[C@@H](c2ccc(Cl)c(Cl)c2)c3ccccc13,\"InChI=1S/C17H17Cl2N/c1-20-17-9-7-12(13-4-2-3-5-14(13)17)11-6-8-15(18)16(19)10-11/h2-6,8,10,12,17,20H,7,9H2,1H3/t12-,17-/m0/s1\",[C][N][C@H1][C][C][C@@H1][Branch1][#C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1],\"(1s,4s)-4-(3,4-dichlorophenyl)-n-methyl-1,2,3,4-tetrahydronaphthalen-1-amine\",3.15\nNC12CCC(CC1)(CC2)c3ccccc3,\"InChI=1S/C14H19N/c15-14-9-6-13(7-10-14,8-11-14)12-4-2-1-3-5-12/h1-5H,6-11,15H2\",[N][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][Branch1][Branch1][C][C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],1-phenylbicyclo[2.2.2]octan-4-amine,0.29\nCCc1nc2c(N)nc3ccccc3c2n1CCCCNS(=O)(=O)C,\"InChI=1S/C17H23N5O2S/c1-3-14-21-15-16(12-8-4-5-9-13(12)20-17(15)18)22(14)11-7-6-10-19-25(2,23)24/h4-5,8-9,19H,3,6-7,10-11H2,1-2H3,(H2,18,20)\",[C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C],\"n-[4-(4-amino-2-ethylimidazo[4,5-c]quinolin-1-yl)butyl]methanesulfonamide\",1.24\nCC(=O)Nc1nnc(s1)S(=O)(=O)N,\"InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)\",[C][C][=Branch1][C][=O][N][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N],\"n-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide\",-0.78\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1C2CCCCC2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C26H31F3N4O5/c1-16(2)21(22(35)26(27,28)29)32-20(34)14-33-23(18-11-7-4-8-12-18)30-13-19(24(33)36)31-25(37)38-15-17-9-5-3-6-10-17/h3,5-6,9-10,13,16,18,21H,4,7-8,11-12,14-15H2,1-2H3,(H,31,37)(H,32,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][C][C][C][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[2-cyclohexyl-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\",2.87\nNc1ccccc1NC(=O)c2ccc(cc2)N3CCOCC3,\"InChI=1S/C17H19N3O2/c18-15-3-1-2-4-16(15)19-17(21)13-5-7-14(8-6-13)20-9-11-22-12-10-20/h1-8H,9-12,18H2,(H,19,21)\",[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],n-(2-aminophenyl)-4-morpholin-4-ylbenzamide,1.2\nO=C(Nc1ccccc1)c2oc3ccccc3c2,\"InChI=1S/C15H11NO2/c17-15(16-12-7-2-1-3-8-12)14-10-11-6-4-5-9-13(11)18-14/h1-10H,(H,16,17)\",[O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2],n-phenyl-1-benzofuran-2-carboxamide,3.44\nCOc1cc2ncnc(Nc3ccc(OCc4ccccn4)c(C)c3)c2cc1OC,\"InChI=1S/C23H22N4O3/c1-15-10-16(7-8-20(15)30-13-17-6-4-5-9-24-17)27-23-18-11-21(28-2)22(29-3)12-19(18)25-14-26-23/h4-12,14H,13H2,1-3H3,(H,25,26,27)\",[C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][C][=C][Ring1][#C][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C],\"6,7-dimethoxy-n-[3-methyl-4-(pyridin-2-ylmethoxy)phenyl]quinazolin-4-amine\",3.6\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccc(F)cc2)NC(=O)OCc3ccncc3)C(=O)C(F)(F)F,\"InChI=1S/C25H23F4N5O5/c1-14(2)20(21(36)25(27,28)29)33-19(35)12-34-22(16-3-5-17(26)6-4-16)31-11-18(23(34)37)32-24(38)39-13-15-7-9-30-10-8-15/h3-11,14,20H,12-13H2,1-2H3,(H,32,38)(H,33,35)\",[C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][P][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"pyridin-4-ylmethyl n-[2-(4-fluorophenyl)-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\",2.22\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(F)cccc34,\"InChI=1S/C21H17FN2O2/c1-12-6-7-18-16(10-12)20(13(2)24(18)11-19(25)26)14-8-9-23-21-15(14)4-3-5-17(21)22/h3-10H,11H2,1-2H3,(H,25,26)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][O][Ring1][#Branch1],\"2-[3-(8-fluoroquinolin-4-yl)-2,5-dimethylindol-1-yl]acetic acid\",0.53\nCOc1ccc2c(c1)c(CC(=O)O)c(C)n2c3ccnc4cc(Cl)ccc34,\"InChI=1S/C21H17ClN2O3/c1-12-16(11-21(25)26)17-10-14(27-2)4-6-19(17)24(12)20-7-8-23-18-9-13(22)3-5-15(18)20/h3-10H,11H2,1-2H3,(H,25,26)\",[C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][=C][Branch1][C][C][N][Ring1][O][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1],2-[1-(7-chloroquinolin-4-yl)-5-methoxy-2-methylindol-3-yl]acetic acid,1.68\nCOc1cccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)c1,\"InChI=1S/C19H20N6O4/c1-27-15-4-2-3-13(11-15)22-19-24-23-18(29-19)17(26)21-14-5-6-16(20-12-14)25-7-9-28-10-8-25/h2-6,11-12H,7-10H2,1H3,(H,21,26)(H,22,24)\",[C][O][C][=C][C][=C][C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][O],\"5-[(3-methoxyphenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\",2.8\nCC(C)Oc1cc(OCCCN2CCCC2)cc3ncnc(Nc4c(Cl)ccc5OCOc45)c13,\"InChI=1S/C25H29ClN4O4/c1-16(2)34-21-13-17(31-11-5-10-30-8-3-4-9-30)12-19-22(21)25(28-14-27-19)29-23-18(26)6-7-20-24(23)33-15-32-20/h6-7,12-14,16H,3-5,8-11,15H2,1-2H3,(H,27,28,29)\",[C][C][Branch1][C][C][O][C][=C][C][Branch1][N][O][C][C][C][N][C][C][C][C][Ring1][Branch1][=C][C][=N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=C][Ring2][Ring1][=C][Ring1][P],\"n-(5-chloro-1,3-benzodioxol-4-yl)-5-propan-2-yloxy-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine\",3.1\nCCN(CC)CCOc1ccc(cc1OC)N(C)C(=O)c2ccc(cc2)c3ccc(cc3)C(F)(F)F,\"InChI=1S/C28H31F3N2O3/c1-5-33(6-2)17-18-36-25-16-15-24(19-26(25)35-4)32(3)27(34)22-9-7-20(8-10-22)21-11-13-23(14-12-21)28(29,30)31/h7-16,19H,5-6,17-18H2,1-4H3\",[C][C][N][Branch1][Ring1][C][C][C][C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],n-[4-(2-diethylaminoethoxy)-3-methoxyphenyl]-n-methyl-4-[4-(trifluoromethyl)phenyl]benzamide,3.13\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(Cl)cccc34,\"InChI=1S/C21H17ClN2O2/c1-12-6-7-18-16(10-12)20(13(2)24(18)11-19(25)26)14-8-9-23-21-15(14)4-3-5-17(21)22/h3-10H,11H2,1-2H3,(H,25,26)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][O][Ring1][#Branch1],\"2-[3-(8-chloroquinolin-4-yl)-2,5-dimethylindol-1-yl]acetic acid\",1.27\nCOc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3occc3,\"InChI=1S/C18H19NO4/c1-22-15-6-4-13(5-7-15)17(20)14-8-10-19(11-9-14)18(21)16-3-2-12-23-16/h2-7,12,14H,8-11H2,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1],[1-(furan-2-carbonyl)piperidin-4-yl]-(4-methoxyphenyl)methanone,2.42\nCN1SC(=NC1=O)NCc2ccccc2,\"InChI=1S/C10H11N3OS/c1-13-10(14)12-9(15-13)11-7-8-5-3-2-4-6-8/h2-6H,7H2,1H3,(H,11,12,14)\",[C][N][S][C][=Branch1][=Branch1][=N][C][Ring1][Branch1][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-methyl-5-(phenylmethylamino)-1,2,4-thiadiazol-3-one\",1.2\nCC(C)N1CCC[C@H](CN2C(=Nc3ccc(cc3C2=O)c4ccc(Cl)cc4)C)C1,\"InChI=1S/C24H28ClN3O/c1-16(2)27-12-4-5-18(14-27)15-28-17(3)26-23-11-8-20(13-22(23)24(28)29)19-6-9-21(25)10-7-19/h6-11,13,16,18H,4-5,12,14-15H2,1-3H3/t18-/m0/s1\",[C][C][Branch1][C][C][N][C][C][C][C@H1][Branch2][Ring2][C][C][N][C][=Branch2][Ring1][O][=N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch2],6-(4-chlorophenyl)-2-methyl-3-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]quinazolin-4-one,3.3\nNc1ncc2cc(c(N)nc2n1)c3c(Br)cccc3Br,\"InChI=1S/C13H9Br2N5/c14-8-2-1-3-9(15)10(8)7-4-6-5-18-13(17)20-12(6)19-11(7)16/h1-5H,(H4,16,17,18,19,20)\",[N][C][=N][C][=C][C][=C][Branch1][N][C][Branch1][C][N][=N][C][Ring1][#Branch1][=N][Ring1][O][C][=C][Branch1][C][Br][C][=C][C][=C][Ring1][#Branch1][Br],\"6-(2,6-dibromophenyl)pyrido[6,5-d]pyrimidine-2,7-diamine\",2.06\nCc1cc(C)c2c(N)c(sc2n1)C(=O)NCc3ccccc3,\"InChI=1S/C17H17N3OS/c1-10-8-11(2)20-17-13(10)14(18)15(22-17)16(21)19-9-12-6-4-3-5-7-12/h3-8H,9,18H2,1-2H3,(H,19,21)\",[C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][N][=C][Branch1][Branch2][S][C][Ring1][=Branch1][=N][Ring1][O][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-amino-4,6-dimethyl-n-(phenylmethyl)thieno[5,4-b]pyridine-2-carboxamide\",3.41\nNc1ncnc2sccc12,\"InChI=1S/C6H5N3S/c7-5-4-1-2-10-6(4)9-3-8-5/h1-3H,(H2,7,8,9)\",[N][C][=N][C][=N][C][S][C][=C][C][Ring1][=Branch2][=Ring1][Branch1],\"thieno[3,2-e]pyrimidin-4-amine\",1.19\nCC(O)(C(=O)Nc1ccc2c(c1)c3ccccc3S2(=O)=O)C(F)(F)F,\"InChI=1S/C16H12F3NO4S/c1-15(22,16(17,18)19)14(21)20-9-6-7-13-11(8-9)10-4-2-3-5-12(10)25(13,23)24/h2-8,22H,1H3,(H,20,21)\",[C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][#Branch2][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F],\"n-(5,5-dioxodibenzothiophen-2-yl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",3\nCC(C)(C(=O)O)c1ccc(cc1)C(O)CCCN2CCC(CC2)C(O)(c3ccccc3)c4ccccc4,\"InChI=1S/C32H39NO4/c1-31(2,30(35)36)25-17-15-24(16-18-25)29(34)14-9-21-33-22-19-28(20-23-33)32(37,26-10-5-3-6-11-26)27-12-7-4-8-13-27/h3-8,10-13,15-18,28-29,34,37H,9,14,19-23H2,1-2H3,(H,35,36)\",[C][C][Branch1][C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-[1-hydroxy-4-[4-[hydroxy-di(phenyl)methyl]piperidin-1-yl]butyl]phenyl]-2-methylpropanoic acid,0.42\nOC[C@H](O)C(=O)N1CCC(=CC1)c2ccc(cc2F)N3C[C@H](COc4ccon4)OC3=O,\"InChI=1S/C21H22FN3O7/c22-17-9-14(25-10-15(32-21(25)29)12-30-19-5-8-31-23-19)1-2-16(17)13-3-6-24(7-4-13)20(28)18(27)11-26/h1-3,5,8-9,15,18,26-27H,4,6-7,10-12H2/t15-,18+/m1/s1\",[O][C][C@H1][Branch1][C][O][C][=Branch1][C][=O][N][C][C][C][=Branch1][Branch1][=C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][N][C][C@H1][Branch1][#Branch2][C][O][C][C][=C][O][N][=Ring1][Branch1][O][C][Ring1][N][=O],\"(5r)-3-[4-[1-[(2s)-2,3-dihydroxypropanoyl]-3,6-dihydro-2h-pyridin-4-yl]-3-fluorophenyl]-5-(1,2-oxazol-3-yloxymethyl)-1,3-oxazolidin-2-one\",1.09\nCOc1c2OC(=O)C=Cc2cc3ccoc13,\"InChI=1S/C12H8O4/c1-14-12-10-8(4-5-15-10)6-7-2-3-9(13)16-11(7)12/h2-6H,1H3\",[C][O][C][=C][O][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][=C][C][C][=C][O][C][Ring1][=C][=Ring1][Branch1],\"9-methoxyfuro[3,2-g]chromen-7-one\",1.97\nOCCNCc1cc(Br)ccc1OCc2ccc(Cl)cc2,\"InChI=1S/C16H17BrClNO2/c17-14-3-6-16(13(9-14)10-19-7-8-20)21-11-12-1-4-15(18)5-2-12/h1-6,9,19-20H,7-8,10-11H2\",[O][C][C][N][C][C][=C][C][Branch1][C][Br][=C][C][=C][Ring1][#Branch1][O][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[[5-bromo-2-[(4-chlorophenyl)methoxy]phenyl]methylamino]ethanol,2.98\nFC(F)Oc1ccc(cc1OCC2CC2)C(=O)Nc3c(Cl)cncc3Cl,\"InChI=1S/C17H14Cl2F2N2O3/c18-11-6-22-7-12(19)15(11)23-16(24)10-3-4-13(26-17(20)21)14(5-10)25-8-9-1-2-9/h3-7,9,17H,1-2,8H2,(H,22,23,24)\",[F][C][Branch1][C][F][O][C][=C][C][=C][Branch1][N][C][=C][Ring1][=Branch1][O][C][C][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=N][C][=C][Ring1][#Branch1][Cl],\"3-(cyclopropylmethoxy)-n-(3,5-dichloropyridin-4-yl)-4-(difluoromethoxy)benzamide\",3.95\nCc1cccc(C(=O)N)c1NC(=O)c2ccccc2,\"InChI=1S/C15H14N2O2/c1-10-6-5-9-12(14(16)18)13(10)17-15(19)11-7-3-2-4-8-11/h2-9H,1H3,(H2,16,18)(H,17,19)\",[C][C][=C][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Ring1][=Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(benzoylamino)-3-methylbenzamide,1.09\nCc1nnc(N)s1,\"InChI=1S/C3H5N3S/c1-2-5-6-3(4)7-2/h1H3,(H2,4,6)\",[C][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1],\"5-methyl-1,3,4-thiadiazol-2-amine\",-0.4\nCC(C)Oc1cc(Oc2ccc(cc2)S(=O)(=O)C)cc(c1)C(=O)Nc3nccs3,\"InChI=1S/C20H20N2O5S2/c1-13(2)26-16-10-14(19(23)22-20-21-8-9-28-20)11-17(12-16)27-15-4-6-18(7-5-15)29(3,24)25/h4-13H,1-3H3,(H,21,22,23)\",[C][C][Branch1][C][C][O][C][=C][C][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][Ring2][=C][Ring1][P][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"3-(4-methylsulfonylphenoxy)-5-propan-2-yloxy-n-(1,3-thiazol-2-yl)benzamide\",3.61\nNS(=O)(=O)c1ccc(CCNc2ccc3nnc(c4ccccc4)n3n2)cc1,\"InChI=1S/C19H18N6O2S/c20-28(26,27)16-8-6-14(7-9-16)12-13-21-17-10-11-18-22-23-19(25(18)24-17)15-4-2-1-3-5-15/h1-11H,12-13H2,(H,21,24)(H2,20,26,27)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][C][C][N][C][C][=C][C][=N][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O][N][=Ring1][#C][C][=C][Ring2][Ring1][Branch2],\"4-[2-[(3-phenyl-[1,2,4]triazolo[3,4-f]pyridazin-6-yl)amino]ethyl]benzenesulfonamide\",2.19\nCCc1ccc(CCOc2ccc(CC3SC(=O)NC3=O)cc2)nc1,\"InChI=1S/C19H20N2O3S/c1-2-13-3-6-15(20-12-13)9-10-24-16-7-4-14(5-8-16)11-17-18(22)21-19(23)25-17/h3-8,12,17H,2,9-11H2,1H3,(H,21,22,23)\",[C][C][C][=C][C][=C][Branch2][Ring1][#Branch2][C][C][O][C][=C][C][=C][Branch1][=N][C][C][S][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=O][C][=C][Ring1][=C][N][=C][Ring2][Ring1][#Branch1],\"5-[[4-[2-(5-ethylpyridin-2-yl)ethoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione\",2.8\nCC[C@H](NC(=O)c1c(N)c(nc2ccccc12)c3cccc(F)c3)c4ccccc4,\"InChI=1S/C25H22FN3O/c1-2-20(16-9-4-3-5-10-16)29-25(30)22-19-13-6-7-14-21(19)28-24(23(22)27)17-11-8-12-18(26)15-17/h3-15,20H,2,27H2,1H3,(H,29,30)/t20-/m0/s1\",[C][C][C@H1][Branch2][Ring2][Ring2][N][C][=Branch1][C][=O][C][=C][Branch1][C][N][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-amino-2-(3-fluorophenyl)-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,4.05\nCN1C(=O)C=C(CCc2ccccc2)N=C1N,\"InChI=1S/C13H15N3O/c1-16-12(17)9-11(15-13(16)14)8-7-10-5-3-2-4-6-10/h2-6,9H,7-8H2,1H3,(H2,14,15)\",[C][N][C][=Branch1][C][=O][C][=C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][#C][N],2-amino-3-methyl-6-(2-phenylethyl)pyrimidin-4-one,2\nCN(C)c1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C25H32Cl2N4O4S/c1-29(2)18-3-6-22(7-4-18)36(33,34)28-25(32)31-13-9-19(10-14-31)30-15-11-20(12-16-30)35-21-5-8-23(26)24(27)17-21/h3-8,17,19-20H,9-16H2,1-2H3,(H,28,32)\",[C][N][Branch1][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(4-dimethylaminophenyl)sulfonylpiperidine-1-carboxamide\",1.7\nCOc1cc2ncnc(Nc3ccc(Cl)c(O)c3)c2cc1OC,\"InChI=1S/C16H14ClN3O3/c1-22-14-6-10-12(7-15(14)23-2)18-8-19-16(10)20-9-3-4-11(17)13(21)5-9/h3-8,21H,1-2H3,(H,18,19,20)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][O][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C],\"2-chloro-5-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol\",3.3\nNc1nc(N)c2cc(NCc3ccc(Cl)c(Cl)c3)ccc2n1,\"InChI=1S/C15H13Cl2N5/c16-11-3-1-8(5-12(11)17)7-20-9-2-4-13-10(6-9)14(18)22-15(19)21-13/h1-6,20H,7H2,(H4,18,19,21,22)\",[N][C][=N][C][Branch1][C][N][=C][C][=C][Branch1][P][N][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][C][Ring1][S][=N][Ring2][Ring1][Branch1],\"n6-[(3,4-dichlorophenyl)methyl]quinazoline-2,4,6-triamine\",2.22\nOC1(CCN(Cc2c[nH]c3ccccc23)CC1)c4ccc(Cl)cc4,\"InChI=1S/C20H21ClN2O/c21-17-7-5-16(6-8-17)20(24)9-11-23(12-10-20)14-15-13-22-19-4-2-1-3-18(15)19/h1-8,13,22,24H,9-12,14H2\",[O][C][Branch2][Ring1][Branch2][C][C][N][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][C][Ring1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],4-(4-chlorophenyl)-1-(1h-indol-3-ylmethyl)piperidin-4-ol,2.25\nCCNCc1cnc(s1)c2ccc(cc2)C(=O)Nc3ccccc3N,\"InChI=1S/C19H20N4OS/c1-2-21-11-15-12-22-19(25-15)14-9-7-13(8-10-14)18(24)23-17-6-4-3-5-16(17)20/h3-10,12,21H,2,11,20H2,1H3,(H,23,24)\",[C][C][N][C][C][=C][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N],\"n-(2-aminophenyl)-4-[5-(ethylaminomethyl)-1,3-thiazol-2-yl]benzamide\",0.95\nFC(F)c1nc2ccccc2n1c3nc(nc(n3)N4CCOCC4)N5CCOCC5,\"InChI=1S/C19H21F2N7O2/c20-15(21)16-22-13-3-1-2-4-14(13)28(16)19-24-17(26-5-9-29-10-6-26)23-18(25-19)27-7-11-30-12-8-27/h1-4,15H,5-12H2\",[F][C][Branch1][C][F][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][=N][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"2-(difluoromethyl)-1-[4,6-di(morpholin-4-yl)-1,3,5-triazin-2-yl]benzimidazole\",3.04\nCC1CCN(CC1)C(=O)c2scc3OCCOc23,\"InChI=1S/C13H17NO3S/c1-9-2-4-14(5-3-9)13(15)12-11-10(8-18-12)16-6-7-17-11/h8-9H,2-7H2,1H3\",[C][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][S][C][=C][O][C][C][O][C][=Ring1][=Branch2][Ring1][=Branch1],\"2,3-dihydrothieno[3,4-b][1,4]dioxin-7-yl-(4-methylpiperidin-1-yl)methanone\",2.26\nC[C@H](NC1=NC(=O)C(C)(S1)C(F)(F)F)c2ccccc2F,\"InChI=1S/C13H12F4N2OS/c1-7(8-5-3-4-6-9(8)14)18-11-19-10(20)12(2,21-11)13(15,16)17/h3-7H,1-2H3,(H,18,19,20)/t7-,12?/m0/s1\",[C][C@H1][Branch2][Ring1][=Branch2][N][C][=N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][Ring2][S][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F],\"2-[[(1s)-1-(2-fluorophenyl)ethyl]amino]-5-methyl-5-(trifluoromethyl)-1,3-thiazol-4-one\",3.1\nCOc1ccc(Cl)cc1NC(=O)CCS(=O)(=O)c2ccc(Br)cc2,\"InChI=1S/C16H15BrClNO4S/c1-23-15-7-4-12(18)10-14(15)19-16(20)8-9-24(21,22)13-5-2-11(17)3-6-13/h2-7,10H,8-9H2,1H3,(H,19,20)\",[C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],3-(4-bromophenyl)sulfonyl-n-(5-chloro-2-methoxyphenyl)propanamide,3.4\nNc1ccc(cc1)S(=O)(=O)N2CCCC2,\"InChI=1S/C10H14N2O2S/c11-9-3-5-10(6-4-9)15(13,14)12-7-1-2-8-12/h3-6H,1-2,7-8,11H2\",[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1],4-pyrrolidin-1-ylsulfonylaniline,0.98\nCC[C@H](NC(=O)c1c(N)c(nc2ccccc12)c3ccccc3)c4ccccc4,\"InChI=1S/C25H23N3O/c1-2-20(17-11-5-3-6-12-17)28-25(29)22-19-15-9-10-16-21(19)27-24(23(22)26)18-13-7-4-8-14-18/h3-16,20H,2,26H2,1H3,(H,28,29)/t20-/m0/s1\",[C][C][C@H1][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][Branch1][C][N][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-amino-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,3.89\nCOc1cc2ncnc(N3CC[C@H](C3)Oc4cnc5ccccc5n4)c2cc1OC,\"InChI=1S/C22H21N5O3/c1-28-19-9-15-18(10-20(19)29-2)24-13-25-22(15)27-8-7-14(12-27)30-21-11-23-16-5-3-4-6-17(16)26-21/h3-6,9-11,13-14H,7-8,12H2,1-2H3/t14-/m1/s1\",[C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][C][C@H1][Branch1][Ring2][C][Ring1][Branch1][O][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C],\"6,7-dimethoxy-4-[(3r)-3-quinoxalin-2-yloxypyrrolidin-1-yl]quinazoline\",4.04\nCc1ccc(cc1)n2c(C)cc(C(=O)NS(=O)(=O)c3ccc(C)cc3)c2C,\"InChI=1S/C21H22N2O3S/c1-14-5-9-18(10-6-14)23-16(3)13-20(17(23)4)21(24)22-27(25,26)19-11-7-15(2)8-12-19/h5-13H,1-4H3,(H,22,24)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][=C][C][Branch2][Ring1][Branch2][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][Ring1][C],\"2,5-dimethyl-1-(4-methylphenyl)-n-(4-methylphenyl)sulfonylpyrrole-3-carboxamide\",2.5\nO[C@@H](CNCCCCCCCCCN1CCC(CC1)OC(=O)Nc2ccccc2c3ccccc3)c4ccc(O)c5NC(=O)C=Cc45,\"InChI=1S/C38H48N4O5/c43-34-19-17-31(32-18-20-36(45)41-37(32)34)35(44)27-39-23-11-4-2-1-3-5-12-24-42-25-21-29(22-26-42)47-38(46)40-33-16-10-9-15-30(33)28-13-7-6-8-14-28/h6-10,13-20,29,35,39,43-44H,1-5,11-12,21-27H2,(H,40,46)(H,41,45)/t35-/m0/s1\",[O][C@@H1][Branch2][Ring2][N][C][N][C][C][C][C][C][C][C][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][C][=C][C][Ring1][N][=Ring1][#Branch1],[1-[9-[[(2r)-2-hydroxy-2-(8-hydroxy-2-oxo-1h-quinolin-5-yl)ethyl]amino]nonyl]piperidin-4-yl] n-(2-phenylphenyl)carbamate,2.16\nCOc1c(N2CCO[C@@H](CN(C)C)C2)c(F)cc3C(=O)C(=CN(C4CC4)c13)C(=O)O,\"InChI=1S/C21H26FN3O5/c1-23(2)9-13-10-24(6-7-30-13)18-16(22)8-14-17(20(18)29-3)25(12-4-5-12)11-15(19(14)26)21(27)28/h8,11-13H,4-7,9-10H2,1-3H3,(H,27,28)/t13-/m0/s1\",[C][O][C][=C][Branch1][P][N][C][C][O][C@@H1][Branch1][#Branch1][C][N][Branch1][C][C][C][C][Ring1][#Branch2][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=Branch1][S][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring2][Ring1][=Branch2][=Ring1][#Branch2][C][=Branch1][C][=O][O],1-cyclopropyl-7-[(2s)-2-(dimethylaminomethyl)morpholin-4-yl]-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid,-0.62\nO=C(NC1CCCCC1)c2cccnc2Sc3ccccc3,\"InChI=1S/C18H20N2OS/c21-17(20-14-8-3-1-4-9-14)16-12-7-13-19-18(16)22-15-10-5-2-6-11-15/h2,5-7,10-14H,1,3-4,8-9H2,(H,20,21)\",[O][=C][Branch1][#Branch2][N][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=Branch1],n-cyclohexyl-2-phenylsulfanylpyridine-3-carboxamide,3.01\nC[C@]12CC[C@H]3[C@@H](CCc4cc(O)ccc34)[C@@H]1CC[C@@H]2O,\"InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1\",[C][C@][C][C][C@H1][C@@H1][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C@@H1][Ring1][#C][C][C][C@@H1][Ring2][Ring1][C][O],\"(8r,9s,13s,14s,17s)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol\",3.72\nC[C@]12CC[C@H]3[C@@H](CCc4cc(O)ccc34)[C@@H]1CCC2=O,\"InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1\",[C][C@][C][C][C@H1][C@@H1][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C@@H1][Ring1][#C][C][C][C][Ring2][Ring1][C][=O],\"(8r,9s,13s,14s)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-17-one\",3.4\nC[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(=C(N2C1=O)C(=O)OCOC(=O)C(C)(C)C)SC3CN(C3)C4=NCCS4,\"InChI=1S/C22H31N3O6S2/c1-11-15-14(12(2)26)18(27)25(15)16(19(28)30-10-31-20(29)22(3,4)5)17(11)33-13-8-24(9-13)21-23-6-7-32-21/h11-15,26H,6-10H2,1-5H3/t11-,12-,14-,15-/m1/s1\",[C][C@@H1][Branch1][C][O][C@@H1][C@H1][C@@H1][Branch1][C][C][C][=Branch2][Ring1][=C][=C][Branch1][Branch2][N][Ring1][=Branch1][C][Ring1][Branch2][=O][C][=Branch1][C][=O][O][C][O][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][C][S][C][C][N][Branch1][Ring2][C][Ring1][Ring2][C][=N][C][C][S][Ring1][Branch1],\"2,2-dimethylpropanoyloxymethyl (4r,5s,6s)-3-[1-(4,5-dihydro-1,3-thiazol-2-yl)azetidin-3-yl]sulfanyl-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate\",2.1\nCc1c(c2c(NS(=O)(=O)C)cccc2n1CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3,\"InChI=1S/C18H17ClN2O6S2/c1-11-18(29(26,27)13-8-6-12(19)7-9-13)17-14(20-28(2,24)25)4-3-5-15(17)21(11)10-16(22)23/h3-9,20H,10H2,1-2H3,(H,22,23)\",[C][C][=C][Branch2][Ring1][=N][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Ring1][O][N][Ring1][=C][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[3-(4-chlorophenyl)sulfonyl-4-methanesulfonamido-2-methylindol-1-yl]acetic acid,-0.83\nCC\\C(=C(/c1ccccc1)\\c2ccc(\\C=C\\C(=O)O)cc2)\\c3ccccc3,\"InChI=1S/C25H22O2/c1-2-23(20-9-5-3-6-10-20)25(21-11-7-4-8-12-21)22-16-13-19(14-17-22)15-18-24(26)27/h3-18H,2H2,1H3,(H,26,27)/b18-15+,25-23-\",[C][C][\\C][=Branch2][Ring1][=N][=C][Branch1][=Branch2][/C][=C][C][=C][C][=C][Ring1][=Branch1][\\C][=C][C][=C][Branch1][Branch2][\\C][=C][\\C][=Branch1][C][=O][O][C][=C][Ring1][O][\\C][=C][C][=C][C][=C][Ring1][=Branch1],\"(e)-3-[4-[(z)-1,2-di(phenyl)but-1-enyl]phenyl]prop-2-enoic acid\",3.89\nCCCCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3,\"InChI=1S/C19H20N2O2/c1-2-3-14-17-18(22)20(15-10-6-4-7-11-15)21(19(17)23)16-12-8-5-9-13-16/h4-13,17H,2-3,14H2,1H3\",[C][C][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4-butyl-1,2-di(phenyl)pyrazolidine-3,5-dione\",0.45\nCC(=O)NC1CC2CCCC(C1)N2C(=O)Nc3ccc(Cl)c(c3)C(F)(F)F,\"InChI=1S/C18H21ClF3N3O2/c1-10(26)23-12-7-13-3-2-4-14(8-12)25(13)17(27)24-11-5-6-16(19)15(9-11)18(20,21)22/h5-6,9,12-14H,2-4,7-8H2,1H3,(H,23,26)(H,24,27)\",[C][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Branch1][Ring2][C][Ring1][Branch2][N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F],7-acetamido-n-[4-chloro-3-(trifluoromethyl)phenyl]-9-azabicyclo[3.3.1]nonane-9-carboxamide,2.79\nCOc1c(Nc2ccc(nc2C)S(=O)(=O)C)ncnc1OC3CCN(CC3)C(=O)OC(C)C,\"InChI=1S/C21H29N5O6S/c1-13(2)31-21(27)26-10-8-15(9-11-26)32-20-18(30-4)19(22-12-23-20)25-16-6-7-17(24-14(16)3)33(5,28)29/h6-7,12-13,15H,8-11H2,1-5H3,(H,22,23,25)\",[C][O][C][=C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][N][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][N][=C][N][=C][Ring2][Ring1][C][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][C][C],propan-2-yl 4-[5-methoxy-6-[(2-methyl-6-methylsulfonylpyridin-3-yl)amino]pyrimidin-4-yl]oxypiperidine-1-carboxylate,2.4\nC[C@H](Nc1nc(Nc2cc(C)[nH]n2)cc(n1)N3CCOCC3)c4ncc(F)cn4,\"InChI=1S/C18H22FN9O/c1-11-7-15(27-26-11)23-14-8-16(28-3-5-29-6-4-28)25-18(24-14)22-12(2)17-20-9-13(19)10-21-17/h7-10,12H,3-6H2,1-2H3,(H3,22,23,24,25,26,27)/t12-/m0/s1\",[C][C@H1][Branch2][Ring1][P][N][C][=N][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=C][C][=Branch1][Ring2][=N][Ring1][=N][N][C][C][O][C][C][Ring1][=Branch1][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1],\"n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-n'-(5-methyl-1h-pyrazol-3-yl)-6-morpholin-4-ylpyrimidine-2,4-diamine\",1.91\nCOc1ccc(NC(=O)CSc2nnc(C)n2c3ccc(C)cc3)cc1,\"InChI=1S/C19H20N4O2S/c1-13-4-8-16(9-5-13)23-14(2)21-22-19(23)26-12-18(24)20-15-6-10-17(25-3)11-7-15/h4-11H,12H2,1-3H3,(H,20,24)\",[C][O][C][=C][C][=C][Branch2][Ring1][=N][N][C][=Branch1][C][=O][C][S][C][=N][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][Branch2],\"n-(4-methoxyphenyl)-2-[[5-methyl-4-(4-methylphenyl)-1,2,4-triazol-3-yl]sulfanyl]acetamide\",2.94\nCC1CC(CN)CC(CO)C1,\"InChI=1S/C9H19NO/c1-7-2-8(5-10)4-9(3-7)6-11/h7-9,11H,2-6,10H2,1H3\",[C][C][C][C][Branch1][Ring1][C][N][C][C][Branch1][Ring1][C][O][C][Ring1][#Branch2],[3-(aminomethyl)-5-methylcyclohexyl]methanol,-1.4\nFC(F)(F)c1nnc2ccc(NCc3cccnc3)nn12,\"InChI=1S/C12H9F3N6/c13-12(14,15)11-19-18-10-4-3-9(20-21(10)11)17-7-8-2-1-5-16-6-8/h1-6H,7H2,(H,17,20)\",[F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][Branch1][O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][=N][N][Ring1][P][Ring1][=C],\"n-(pyridin-3-ylmethyl)-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazin-6-amine\",2.06\nCCN(CC)CCOC(=O)C1(CCCC1)c2ccccc2,\"InChI=1S/C18H27NO2/c1-3-19(4-2)14-15-21-17(20)18(12-8-9-13-18)16-10-6-5-7-11-16/h5-7,10-11H,3-4,8-9,12-15H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][C][O][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-diethylaminoethyl 1-phenylcyclopentane-1-carboxylate,2.3\nOC1(CNCCc2ccccc12)c3ccccc3,\"InChI=1S/C16H17NO/c18-16(14-7-2-1-3-8-14)12-17-11-10-13-6-4-5-9-15(13)16/h1-9,17-18H,10-12H2\",[O][C][Branch1][#C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-phenyl-2,3,4,5-tetrahydro-3-benzazepin-1-ol\",1.38\nCC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3CCOCC3)c(F)c2,\"InChI=1S/C16H20FN3O4/c1-11(21)18-9-13-10-20(16(22)24-13)12-2-3-15(14(17)8-12)19-4-6-23-7-5-19/h2-3,8,13H,4-7,9-10H2,1H3,(H,18,21)/t13-/m0/s1\",[C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][=C][Ring1][=N],\"n-[[(5s)-3-(3-fluoro-4-morpholin-4-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\",0.67\nCc1cnc(NC(=O)Cc2ccccc2)s1,\"InChI=1S/C12H12N2OS/c1-9-8-13-12(16-9)14-11(15)7-10-5-3-2-4-6-10/h2-6,8H,7H2,1H3,(H,13,14,15)\",[C][C][=C][N][=C][Branch1][#C][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][#C],\"n-(5-methyl-1,3-thiazol-2-yl)-2-phenylacetamide\",2.9\nc1ccc2ncncc2c1,InChI=1S/C8H6N2/c1-2-4-8-7(3-1)5-9-6-10-8/h1-6H,[C][=C][C][=C][N][=C][N][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],quinazoline,1\nO[C@@H](CNCCSCCCOCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H28N2O4S2/c25-18-8-7-17(21-20(18)24-22(27)30-21)19(26)15-23-10-14-29-13-4-11-28-12-9-16-5-2-1-3-6-16/h1-3,5-8,19,23,25-26H,4,9-15H2,(H,24,27)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][S][C][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(2-phenylethoxy)propylsulfanyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\",2.54\nCCC(C)(C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@@H]12,\"InChI=1S/C25H38O5/c1-6-25(4,5)24(28)30-21-12-15(2)11-17-8-7-16(3)20(23(17)21)10-9-19-13-18(26)14-22(27)29-19/h7-8,11,15-16,18-21,23,26H,6,9-10,12-14H2,1-5H3/t15-,16-,18+,19+,20-,21-,23-/m0/s1\",[C][C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@@H1][Branch1][C][C][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch1][P][C][C][C@@H1][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][Ring1][Branch2][C@@H1][Ring2][Ring1][=Branch1][Ring1][P],\"[(1s,3r,7s,8s,8ar)-8-[2-[(2r,4r)-4-hydroxy-6-oxooxan-2-yl]ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2,2-dimethylbutanoate\",3.7\nC[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc3ccccc3Cl,\"InChI=1S/C22H24Cl2N2O4/c1-15-12-25(13-17-10-18(23)6-7-20(17)30-14-22(28)29)8-9-26(15)21(27)11-16-4-2-3-5-19(16)24/h2-7,10,15H,8-9,11-14H2,1H3,(H,28,29)/t15-/m0/s1\",[C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],2-[4-chloro-2-[[(3s)-4-[2-(2-chlorophenyl)acetyl]-3-methylpiperazin-1-yl]methyl]phenoxy]acetic acid,1.1\nCC[C@@H](NC1=C(Nc2cccc(C(=O)N(C)C)c2O)C(=O)C1=O)c3ccccc3,\"InChI=1S/C22H23N3O4/c1-4-15(13-9-6-5-7-10-13)23-17-18(21(28)20(17)27)24-16-12-8-11-14(19(16)26)22(29)25(2)3/h5-12,15,23-24,26H,4H2,1-3H3/t15-/m1/s1\",[C][C][C@@H1][Branch2][Ring2][Branch1][N][C][=C][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][Branch1][#Branch2][C][=Branch1][C][=O][N][Branch1][C][C][C][=C][Ring1][O][O][C][=Branch1][C][=O][C][Ring2][Ring1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-[[3,4-dioxo-2-[[(1r)-1-phenylpropyl]amino]-1-cyclobutenyl]amino]-2-hydroxy-n,n-dimethylbenzamide\",2.14\nCc1ccc(NC(=O)c2cccc(c2)N3CCOCC3)cc1NC(=O)c4ccc(OCc5ccccn5)cc4,\"InChI=1S/C31H30N4O4/c1-22-8-11-25(33-31(37)24-5-4-7-27(19-24)35-15-17-38-18-16-35)20-29(22)34-30(36)23-9-12-28(13-10-23)39-21-26-6-2-3-14-32-26/h2-14,19-20H,15-18,21H2,1H3,(H,33,37)(H,34,36)\",[C][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring1][=C],n-[4-methyl-3-[[4-(pyridin-2-ylmethoxy)benzoyl]amino]phenyl]-3-morpholin-4-ylbenzamide,3.2\nNC1=NC(Nc2c(F)ccc(F)c12)c3occc3,\"InChI=1S/C12H9F2N3O/c13-6-3-4-7(14)10-9(6)11(15)17-12(16-10)8-2-1-5-18-8/h1-5,12,16H,(H2,15,17)\",[N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][F][C][=C][C][Branch1][C][F][=C][Ring1][N][Ring1][Branch2][C][O][C][=C][C][=Ring1][Branch1],\"5,8-difluoro-2-furan-2-yl-1,2-dihydroquinazolin-4-amine\",1.2\nCC(C)NC(=O)c1cnc(N2CCC(CC2)N3C(=O)OCc4ccccc34)c(Cl)c1,\"InChI=1S/C22H25ClN4O3/c1-14(2)25-21(28)16-11-18(23)20(24-12-16)26-9-7-17(8-10-26)27-19-6-4-3-5-15(19)13-30-22(27)29/h3-6,11-12,14,17H,7-10,13H2,1-2H3,(H,25,28)\",[C][C][Branch1][C][C][N][C][=Branch1][C][=O][C][=C][N][=C][Branch2][Ring1][N][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2],\"5-chloro-6-[4-(2-oxo-4h-3,1-benzoxazin-1-yl)piperidin-1-yl]-n-propan-2-ylpyridine-3-carboxamide\",3.57\nFc1ccc(cc1)C(=O)C2CCN(CCN3C(=O)Nc4ccccc4C3=O)CC2,\"InChI=1S/C22H22FN3O3/c23-17-7-5-15(6-8-17)20(27)16-9-11-25(12-10-16)13-14-26-21(28)18-3-1-2-4-19(18)24-22(26)29/h1-8,16H,9-14H2,(H,24,29)\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch2][Ring1][Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=O][C][C][Ring2][Ring1][Ring2],\"3-[2-[4-(4-fluorobenzoyl)piperidin-1-yl]ethyl]-1h-quinazoline-2,4-dione\",2.9\nO=C1Nc2ccccc2C=C1,\"InChI=1S/C9H7NO/c11-9-6-5-7-3-1-2-4-8(7)10-9/h1-6H,(H,10,11)\",[O][=C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2],1h-quinolin-2-one,1.32\nCOc1ccc(CNC(=O)c2sc3nc(C)cc(C)c3c2N)cc1,\"InChI=1S/C18H19N3O2S/c1-10-8-11(2)21-18-14(10)15(19)16(24-18)17(22)20-9-12-4-6-13(23-3)7-5-12/h4-8H,9,19H2,1-3H3,(H,20,22)\",[C][O][C][=C][C][=C][Branch2][Ring1][O][C][N][C][=Branch1][C][=O][C][S][C][=N][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2][C][=Ring1][O][N][C][=C][Ring2][Ring1][=Branch1],\"3-amino-n-[(4-methoxyphenyl)methyl]-4,6-dimethylthieno[5,4-b]pyridine-2-carboxamide\",3.85\nCOc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3ccc(F)cc3,\"InChI=1S/C20H20FNO3/c1-25-18-8-4-14(5-9-18)19(23)15-10-12-22(13-11-15)20(24)16-2-6-17(21)7-3-16/h2-9,15H,10-13H2,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],[1-(4-fluorobenzoyl)piperidin-4-yl]-(4-methoxyphenyl)methanone,2.92\nCC(C)NC[C@@H](C(=O)N1CCN(CC1)c2ncnc3[C@H](O)C[C@@H](C)c23)c4ccc(Cl)cc4,\"InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1\",[C][C][Branch1][C][C][N][C][C@@H1][Branch2][Ring2][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=N][C][C@H1][Branch1][C][O][C][C@@H1][Branch1][C][C][C][Ring1][O][=Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"(2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[e]pyrimidin-4-yl]piperazin-1-yl]-3-(propan-2-ylamino)propan-1-one\",1.3\nCOc1cc(ccc1Cn2ncc3ccc(NC(=O)OC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5,\"InChI=1S/C28H28N4O6S/c1-37-26-15-19(27(33)31-39(35,36)24-9-3-2-4-10-24)11-12-21(26)18-32-25-16-22(14-13-20(25)17-29-32)30-28(34)38-23-7-5-6-8-23/h2-4,9-17,23H,5-8,18H2,1H3,(H,30,34)(H,31,33)\",[C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][N][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],cyclopentyl n-[1-[[2-methoxy-4-(phenylsulfonylcarbamoyl)phenyl]methyl]indazol-6-yl]carbamate,1.8\nNC1C2CN(CC12)c3nc4N(C=C(C(=O)O)C(=O)c4cc3F)c5ccc(F)cc5F,\"InChI=1S/C20H15F3N4O3/c21-8-1-2-15(13(22)3-8)27-7-12(20(29)30)17(28)9-4-14(23)19(25-18(9)27)26-5-10-11(6-26)16(10)24/h1-4,7,10-11,16H,5-6,24H2,(H,29,30)\",[N][C][C][C][N][Branch1][#Branch1][C][C][Ring1][=Branch1][Ring1][Branch1][C][=N][C][N][Branch2][Ring1][=Branch1][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=Ring1][#Branch2][C][=C][Ring1][=C][F][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F],\"7-(6-amino-3-azabicyclo[3.1.0]hexan-3-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid\",0.3\n[O-][N+](=O)c1ccc2c(c1)nc3CCCCCn23,\"InChI=1S/C12H13N3O2/c16-15(17)9-5-6-11-10(8-9)13-12-4-2-1-3-7-14(11)12/h5-6,8H,1-4,7H2\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=C][C][C][C][C][C][N][Ring1][O][Ring1][#Branch1],\"3-nitro-7,8,9,10-tetrahydro-6h-azepino[1,2-a]benzimidazole\",2.58\nOc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1,\"InChI=1S/C23H27N5O5/c29-17-2-4-19-18(11-17)28(22(31)14-33-19)10-9-27-7-5-15(6-8-27)24-12-16-1-3-20-23(25-16)26-21(30)13-32-20/h1-4,11,15,24,29H,5-10,12-14H2,(H,25,26,30)\",[O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S],\"6-[[[1-[2-(6-hydroxy-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",0.52\nCOc1ccc2c(C)cc(N[C@H]3CCC[C@@H](C3)NCc4cccc(OC(F)(F)F)c4)nc2c1,\"InChI=1S/C25H28F3N3O2/c1-16-11-24(31-23-14-20(32-2)9-10-22(16)23)30-19-7-4-6-18(13-19)29-15-17-5-3-8-21(12-17)33-25(26,27)28/h3,5,8-12,14,18-19,29H,4,6-7,13,15H2,1-2H3,(H,30,31)/t18-,19-/m0/s1\",[C][O][C][=C][C][=C][C][Branch1][C][C][=C][C][Branch2][Ring1][P][N][C@H1][C][C][C][C@@H1][Branch1][Ring2][C][Ring1][=Branch1][N][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][O][=N][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C],\"(1s,3s)-n'-(7-methoxy-4-methylquinolin-2-yl)-n-[[3-(trifluoromethoxy)phenyl]methyl]cyclohexane-1,3-diamine\",3.61\nCOc1cccc(Nc2nc(NCC3CCCO3)c4ccccc4n2)c1,\"InChI=1S/C20H22N4O2/c1-25-15-7-4-6-14(12-15)22-20-23-18-10-3-2-9-17(18)19(24-20)21-13-16-8-5-11-26-16/h2-4,6-7,9-10,12,16H,5,8,11,13H2,1H3,(H2,21,22,23,24)\",[C][O][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=N][C][Branch1][#Branch2][N][C][C][C][C][C][O][Ring1][Branch1][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][P][=C][Ring2][Ring1][Branch2],\"n-(3-methoxyphenyl)-n'-(oxolan-2-ylmethyl)quinazoline-2,4-diamine\",3.9\nCc1ccsc1CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3,\"InChI=1S/C17H12ClN3O3S/c1-8-4-5-25-12(8)7-21-17(24)13-14(16(23)20-21)19-11-6-9(18)2-3-10(11)15(13)22/h2-6H,7H2,1H3,(H,19,22)(H,20,23)\",[C][C][C][=C][S][C][=Ring1][Branch1][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C],\"7-chloro-2-[(3-methylthiophen-2-yl)methyl]-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",1.15\nCc1cc(C)c2c(N)c(sc2n1)C(=O)NC3CC3,\"InChI=1S/C13H15N3OS/c1-6-5-7(2)15-13-9(6)10(14)11(18-13)12(17)16-8-3-4-8/h5,8H,3-4,14H2,1-2H3,(H,16,17)\",[C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][N][=C][Branch1][Branch2][S][C][Ring1][=Branch1][=N][Ring1][O][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring1],\"3-amino-n-cyclopropyl-4,6-dimethylthieno[5,4-b]pyridine-2-carboxamide\",2.53\nCN1C(=O)c2c(onc2c3ccccc3)C=C1c4ccncc4,\"InChI=1S/C18H13N3O2/c1-21-14(12-7-9-19-10-8-12)11-15-16(18(21)22)17(20-23-15)13-5-3-2-4-6-13/h2-11H,1H3\",[C][N][C][=Branch1][C][=O][C][=C][Branch1][=C][O][N][=C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=N][C][=C][Ring1][=Branch1],\"5-methyl-3-phenyl-6-pyridin-4-yl-[1,2]oxazolo[4,5-c]pyridin-4-one\",2.61\nCc1ccc(Nc2c(F)cccc2Cl)c(CC(=O)O)c1,\"InChI=1S/C15H13ClFNO2/c1-9-5-6-13(10(7-9)8-14(19)20)18-15-11(16)3-2-4-12(15)17/h2-7,18H,8H2,1H3,(H,19,20)\",[C][C][=C][C][=C][Branch1][=C][N][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][Cl][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][=C][Ring2][Ring1][Ring1],2-[2-[(2-chloro-6-fluorophenyl)amino]-5-methylphenyl]acetic acid,1.02\nCOC(=O)CCC(=O)Nc1ccc2C(=O)C(=O)c3ccccc3c2c1,\"InChI=1S/C19H15NO5/c1-25-17(22)9-8-16(21)20-11-6-7-14-15(10-11)12-4-2-3-5-13(12)18(23)19(14)24/h2-7,10H,8-9H2,1H3,(H,20,21)\",[C][O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S],\"methyl 4-[(9,10-dioxophenanthren-3-yl)amino]-4-oxobutanoate\",2.72\nCCCC(=O)N1CCN(CC1)c2nnc(c3ccccc3)c4ccccc24,\"InChI=1S/C22H24N4O/c1-2-8-20(27)25-13-15-26(16-14-25)22-19-12-7-6-11-18(19)21(23-24-22)17-9-4-3-5-10-17/h3-7,9-12H,2,8,13-16H2,1H3\",[C][C][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1],1-[4-(4-phenylphthalazin-1-yl)piperazin-1-yl]butan-1-one,3.2\nC[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)c3cc4c(cn(C)c4cc3Cl)C(=O)C(=O)N(C)C,\"InChI=1S/C27H30ClFN4O3/c1-16-13-33(17(2)12-32(16)14-18-6-8-19(29)9-7-18)26(35)21-10-20-22(25(34)27(36)30(3)4)15-31(5)24(20)11-23(21)28/h6-11,15-17H,12-14H2,1-5H3/t16-,17+/m0/s1\",[C][C@@H1][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C@@H1][Branch1][C][C][C][N][Ring1][#C][C][=Branch1][C][=O][C][=C][C][C][=Branch1][=C][=C][N][Branch1][C][C][C][=Ring1][=Branch1][C][=C][Ring1][#Branch2][Cl][C][=Branch1][C][=O][C][=Branch1][C][=O][N][Branch1][C][C][C],\"2-[6-chloro-5-[(2r,5s)-4-[(4-fluorophenyl)methyl]-2,5-dimethylpiperazine-1-carbonyl]-1-methylindol-3-yl]-n,n-dimethyl-2-oxoacetamide\",3.6\nCN1SC(=NC1=O)NC(=O)c2ccccc2,\"InChI=1S/C10H9N3O2S/c1-13-10(15)12-9(16-13)11-8(14)7-5-3-2-4-6-7/h2-6H,1H3,(H,11,12,14,15)\",[C][N][S][C][=Branch1][=Branch1][=N][C][Ring1][Branch1][=O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-(2-methyl-3-oxo-1,2,4-thiadiazol-5-yl)benzamide\",1.13\nC[C@H]1[C@@H]2CN(CCN3CCOCC3)CC[C@H]2Cc4[nH]c5ccc(cc5c14)C(F)(F)F,\"InChI=1S/C23H30F3N3O/c1-15-19-14-29(7-6-28-8-10-30-11-9-28)5-4-16(19)12-21-22(15)18-13-17(23(24,25)26)2-3-20(18)27-21/h2-3,13,15-16,19,27H,4-12,14H2,1H3/t15-,16-,19-/m0/s1\",[C][C@H1][C@@H1][C][N][Branch1][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][C][C@H1][Ring1][=C][C][C][NH1][C][=C][C][=C][Branch1][O][C][=C][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][=Ring1][=Branch2][C][Branch1][C][F][Branch1][C][F][F],\"(4as,11s,11ar)-11-methyl-2-(2-morpholin-4-ylethyl)-9-(trifluoromethyl)-1,3,4,4a,5,6,11,11a-octahydropyrido[4,3-b]carbazole\",2.87\nCC(C)NCC(O)COc1cccc2[nH]ccc12,\"InChI=1S/C14H20N2O2/c1-10(2)16-8-11(17)9-18-14-5-3-4-13-12(14)6-7-15-13/h3-7,10-11,15-17H,8-9H2,1-2H3\",[C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][NH1][C][=C][C][Ring1][=Branch2][=Ring1][Branch1],1-(1h-indol-4-yloxy)-3-(propan-2-ylamino)propan-2-ol,-0.12\nC[C@H](Nc1ncc(C)c(Nc2cc(C)[nH]n2)n1)c3ncc(F)cn3,\"InChI=1S/C15H17FN8/c1-8-5-19-15(20-10(3)14-17-6-11(16)7-18-14)22-13(8)21-12-4-9(2)23-24-12/h4-7,10H,1-3H3,(H3,19,20,21,22,23,24)/t10-/m0/s1\",[C][C@H1][Branch2][Ring1][#Branch2][N][C][=N][C][=C][Branch1][C][C][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=N][Ring1][=C][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1],\"n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-5-methyl-n'-(5-methyl-1h-pyrazol-3-yl)pyrimidine-2,4-diamine\",1.75\nCc1ccccc1Nc2ncnc3ccccc23,\"InChI=1S/C15H13N3/c1-11-6-2-4-8-13(11)18-15-12-7-3-5-9-14(12)16-10-17-15/h2-10H,1H3,(H,16,17,18)\",[C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],n-(2-methylphenyl)quinazolin-4-amine,2.85\nC1CN2C[C@@H](N=C2S1)c3ccccc3,\"InChI=1S/C11H12N2S/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10/h1-5,10H,6-8H2/t10-/m1/s1\",[C][C][N][C][C@@H1][Branch1][Branch2][N][=C][Ring1][Branch1][S][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(6s)-6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole\",0.81\nCOc1ccc(NC(=O)c2ccnc(N)n2)cc1,\"InChI=1S/C12H12N4O2/c1-18-9-4-2-8(3-5-9)15-11(17)10-6-7-14-12(13)16-10/h2-7H,1H3,(H,15,17)(H2,13,14,16)\",[C][O][C][=C][C][=C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=N][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][Ring1][S],2-amino-n-(4-methoxyphenyl)pyrimidine-4-carboxamide,1.72\nCC(C)c1ccccc1Cc2cc(C(=O)Nc3ccc(cc3)S(=O)(=O)c4ccccc4C(C)(C)C)c(O)c(O)c2O,\"InChI=1S/C33H35NO6S/c1-20(2)25-11-7-6-10-21(25)18-22-19-26(30(36)31(37)29(22)35)32(38)34-23-14-16-24(17-15-23)41(39,40)28-13-9-8-12-27(28)33(3,4)5/h6-17,19-20,35-37H,18H2,1-5H3,(H,34,38)\",[C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][Branch2][Ring2][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring2][Ring1][=C][O],\"n-[4-(2-tert-butylphenyl)sulfonylphenyl]-2,3,4-trihydroxy-5-[(2-propan-2-ylphenyl)methyl]benzamide\",3.44\nCN(c1ccnc(Nc2cccc(c2)S(=O)(=O)C)n1)c3cccc4[nH]ncc34,\"InChI=1S/C19H18N6O2S/c1-25(17-8-4-7-16-15(17)12-21-24-16)18-9-10-20-19(23-18)22-13-5-3-6-14(11-13)28(2,26)27/h3-12H,1-2H3,(H,21,24)(H,20,22,23)\",[C][N][Branch2][Ring1][#C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=N][Ring1][P][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1],\"n'-(1h-indazol-4-yl)-n'-methyl-n-(3-methylsulfonylphenyl)pyrimidine-2,4-diamine\",3.21\nCNC(=O)c1ccccc1Sc2ccc3c(\\C=C\\c4ccccn4)n[nH]c3c2,\"InChI=1S/C22H18N4OS/c1-23-22(27)18-7-2-3-8-21(18)28-16-10-11-17-19(25-26-20(17)14-16)12-9-15-6-4-5-13-24-15/h2-14H,1H3,(H,23,27)(H,25,26)/b12-9+\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][Branch1][O][\\C][=C][\\C][=C][C][=C][C][=N][Ring1][=Branch1][=N][NH1][C][Ring1][=N][=C][Ring1][P],n-methyl-2-[[3-[(e)-2-pyridin-2-ylethenyl]-1h-indazol-6-yl]sulfanyl]benzamide,3.8\nCOc1cc(OC)nc(n1)N2N=CC(=C(Cl)C2=O)Cl,\"InChI=1S/C10H8Cl2N4O3/c1-18-6-3-7(19-2)15-10(14-6)16-9(17)8(12)5(11)4-13-16/h3-4H,1-2H3\",[C][O][C][=C][C][Branch1][Ring1][O][C][=N][C][=Branch1][Ring2][=N][Ring1][Branch2][N][N][=C][C][=Branch1][=Branch2][=C][Branch1][C][Cl][C][Ring1][#Branch1][=O][Cl],\"4,5-dichloro-2-(4,6-dimethoxypyrimidin-2-yl)pyridazin-3-one\",1.4\nCN1CCN(CC1)C(=O)c2cc3ccccc3n2C,\"InChI=1S/C15H19N3O/c1-16-7-9-18(10-8-16)15(19)14-11-12-5-3-4-6-13(12)17(14)2/h3-6,11H,7-10H2,1-2H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C],(1-methylindol-2-yl)-(4-methylpiperazin-1-yl)methanone,1.71\nCN(C)CC(O)COc1ccc(Nc2nccc(Nc3ccc(Cl)cc3)n2)cc1,\"InChI=1S/C21H24ClN5O2/c1-27(2)13-18(28)14-29-19-9-7-17(8-10-19)25-21-23-12-11-20(26-21)24-16-5-3-15(22)4-6-16/h3-12,18,28H,13-14H2,1-2H3,(H2,23,24,25,26)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][C][Branch1][=N][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1],1-[4-[[4-[(4-chlorophenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol,2.6\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccccc34)c2C(=O)N5C[C@H](O)CO5,\"InChI=1S/C25H26N4O5S/c1-14(2)11-28-24-21(22(31)27(3)25(28)33)20(23(32)29-12-16(30)13-34-29)19(35-24)10-15-8-9-26-18-7-5-4-6-17(15)18/h4-9,14,16,30H,10-13H2,1-3H3/t16-/m0/s1\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][C][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][O][Ring1][=Branch1],\"5-[(4s)-4-hydroxy1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)-6-(quinolin-4-ylmethyl)thieno[3,2-e]pyrimidine-2,4-dione\",2.14\nO=S(=O)(Cc1cc(nc(n1)c2ccccn2)N3CCOCC3)c4ccccc4,\"InChI=1S/C20H20N4O3S/c25-28(26,17-6-2-1-3-7-17)15-16-14-19(24-10-12-27-13-11-24)23-20(22-16)18-8-4-5-9-21-18/h1-9,14H,10-13,15H2\",[O][=S][=Branch1][C][=O][Branch2][Ring1][=C][C][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],4-morpholin-4-yl-6-(phenylsulfonylmethyl)-2-pyridin-2-ylpyrimidine,1.34\nCCOC(=O)C1(CCN(C)CC1)c2ccccc2,\"InChI=1S/C15H21NO2/c1-3-18-14(17)15(9-11-16(2)12-10-15)13-7-5-4-6-8-13/h4-8H,3,9-12H2,1-2H3\",[C][C][O][C][=Branch1][C][=O][C][Branch1][O][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],ethyl 1-methyl-4-phenylpiperidine-4-carboxylate,1.4\nCNC(=O)C[C@H](Nc1ncc(Cl)c(Nc2cc([nH]n2)C3CC3)n1)c4ccc(F)cc4,\"InChI=1S/C20H21ClFN7O/c1-23-18(30)9-15(11-4-6-13(22)7-5-11)25-20-24-10-14(21)19(27-20)26-17-8-16(28-29-17)12-2-3-12/h4-8,10,12,15H,2-3,9H2,1H3,(H,23,30)(H3,24,25,26,27,28,29)/t15-/m0/s1\",[C][N][C][=Branch1][C][=O][C][C@H1][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][Cl][C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],(3s)-3-[[5-chloro-4-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]pyrimidin-2-yl]amino]-3-(4-fluorophenyl)-n-methylpropanamide,2.23\nOc1cc(O)cc(\\C=C\\c2ccc(O)c(O)c2)c1,\"InChI=1S/C14H12O4/c15-11-5-10(6-12(16)8-11)2-1-9-3-4-13(17)14(18)7-9/h1-8,15-18H/b2-1+\",[O][C][=C][C][Branch1][C][O][=C][C][Branch1][P][\\C][=C][\\C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2][=C][Ring1][P],\"5-[(e)-2-(3,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol\n5-[2-(3,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol\",2.11\nCS(=O)(=O)c1ccc(cc1)[C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl,\"InChI=1S/C12H14Cl2FNO4S/c1-21(19,20)8-4-2-7(3-5-8)10(17)9(6-15)16-12(18)11(13)14/h2-5,9-11,17H,6H2,1H3,(H,16,18)/t9-,10-/m1/s1\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][Branch1][C][O][C@@H1][Branch1][Ring1][C][F][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl],\"2,2-dichloro-n-[(1r,2s)-3-fluoro-1-hydroxy-1-(4-methylsulfonylphenyl)propan-2-yl]acetamide\",0.44\nCCN(CCO)CCCC(C)Nc1ccnc2cc(Cl)ccc12,\"InChI=1S/C18H26ClN3O/c1-3-22(11-12-23)10-4-5-14(2)21-17-8-9-20-18-13-15(19)6-7-16(17)18/h6-9,13-14,23H,3-5,10-12H2,1-2H3,(H,20,21)\",[C][C][N][Branch1][Ring2][C][C][O][C][C][C][C][Branch1][C][C][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1],2-[4-[(7-chloroquinolin-4-yl)amino]pentyl-ethylamino]ethanol,0.77\nC1CC1Nc2ccc3nnc(c4ccccc4)n3n2,\"InChI=1S/C14H13N5/c1-2-4-10(5-3-1)14-17-16-13-9-8-12(18-19(13)14)15-11-6-7-11/h1-5,8-9,11H,6-7H2,(H,15,18)\",[C][C][C][Ring1][Ring1][N][C][C][=C][C][=N][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O][N][=Ring1][#C],\"n-cyclopropyl-3-phenyl-[1,2,4]triazolo[3,4-f]pyridazin-6-amine\",3.15\nCCc1c(C)[nH]c2CCC(CN3CCOCC3)C(=O)c12,\"InChI=1S/C16H24N2O2/c1-3-13-11(2)17-14-5-4-12(16(19)15(13)14)10-18-6-8-20-9-7-18/h12,17H,3-10H2,1-2H3\",[C][C][C][=C][Branch1][C][C][NH1][C][C][C][C][Branch1][#Branch2][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring2][Ring1][C][=Ring1][=C],\"3-ethyl-2-methyl-5-(morpholin-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one\",1.54\nCC(C)OC(=O)C1=CN(Cc2c(F)cccc2F)c3sc(c(CN(C)Cc4ccccc4)c3C1=O)c5ccc(NC(=O)C(C)C)cc5,\"InChI=1S/C37H37F2N3O4S/c1-22(2)35(44)40-26-16-14-25(15-17-26)34-28(19-41(5)18-24-10-7-6-8-11-24)32-33(43)29(37(45)46-23(3)4)21-42(36(32)47-34)20-27-30(38)12-9-13-31(27)39/h6-17,21-23H,18-20H2,1-5H3,(H,40,44)\",[C][C][Branch1][C][C][O][C][=Branch1][C][=O][C][=C][N][Branch1][=C][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][S][C][=Branch2][Ring1][#Branch2][=C][Branch1][#C][C][N][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][#C][C][Ring2][Ring1][N][=O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][C][C][C][=C][Ring1][N],\"propan-2-yl 7-[(2,6-difluorophenyl)methyl]-3-[(methyl-(phenylmethyl)amino)methyl]-2-[4-(2-methylpropanoylamino)phenyl]-4-oxothieno[3,2-e]pyridine-5-carboxylate\",3.5\nClc1cccc(C(=O)N2CCN(CC2)c3ccccn3)c1Cl,\"InChI=1S/C16H15Cl2N3O/c17-13-5-3-4-12(15(13)18)16(22)21-10-8-20(9-11-21)14-6-1-2-7-19-14/h1-7H,8-11H2\",[Cl][C][=C][C][=C][C][Branch2][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring2][Ring1][Ring2][Cl],\"(2,3-dichlorophenyl)-(4-pyridin-2-ylpiperazin-1-yl)methanone\",2.98\nC1Cc2ncc(c3ccc4OCCOc4c3)n2C1,\"InChI=1S/C14H14N2O2/c1-2-14-15-9-11(16(14)5-1)10-3-4-12-13(8-10)18-7-6-17-12/h3-4,8-9H,1-2,5-7H2\",[C][C][C][=N][C][=C][Branch1][#C][C][=C][C][=C][O][C][C][O][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][Ring1][#C][C][Ring2][Ring1][C],\"3-(2,3-dihydro-1,4-benzodioxin-7-yl)-6,7-dihydro-5h-pyrrolo[1,2-a]imidazole\",2.33\nCNC1=Nc2ncccc2C(=NC1c3cccs3)c4occc4,\"InChI=1S/C17H14N4OS/c1-18-17-15(13-7-4-10-23-13)20-14(12-6-3-9-22-12)11-5-2-8-19-16(11)21-17/h2-10,15H,1H3,(H,18,19,21)\",[C][N][C][=N][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][N][=N][C][Ring1][O][C][=C][C][=C][S][Ring1][Branch1][C][O][C][=C][C][=Ring1][Branch1],\"5-furan-2-yl-n-methyl-3-thiophen-2-yl-3h-pyrido[3,2-f][1,4]diazepin-2-amine\",1.85\nCN1CCN(CC1)S(=O)(=O)c2ccc(c3cnc(N)c(n3)C(=O)Nc4cccnc4)c(c2)C(F)(F)F,\"InChI=1S/C22H22F3N7O3S/c1-31-7-9-32(10-8-31)36(34,35)15-4-5-16(17(11-15)22(23,24)25)18-13-28-20(26)19(30-18)21(33)29-14-3-2-6-27-12-14/h2-6,11-13H,7-10H2,1H3,(H2,26,28)(H,29,33)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][Branch1][=C][Ring2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],3-amino-6-[4-(4-methylpiperazin-1-yl)sulfonyl-2-(trifluoromethyl)phenyl]-n-pyridin-3-ylpyrazine-2-carboxamide,3.25\nCC(=O)C1=CN(Cc2ccccc2)C(=O)N(Cc3ccc(F)cc3)C1=O,\"InChI=1S/C20H17FN2O3/c1-14(24)18-13-22(11-15-5-3-2-4-6-15)20(26)23(19(18)25)12-16-7-9-17(21)10-8-16/h2-10,13H,11-12H2,1H3\",[C][C][=Branch1][C][=O][C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Ring2][Ring1][=Branch1][=O],\"5-acetyl-3-[(4-fluorophenyl)methyl]-1-(phenylmethyl)pyrimidine-2,4-dione\",3.2\nCc1sc2ncnc(SCC(=O)N3CCN(CC3)C(=O)c4occc4)c2c1C,\"InChI=1S/C19H20N4O3S2/c1-12-13(2)28-18-16(12)17(20-11-21-18)27-10-15(24)22-5-7-23(8-6-22)19(25)14-4-3-9-26-14/h3-4,9,11H,5-8,10H2,1-2H3\",[C][C][S][C][=N][C][=N][C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][=C][Ring2][Ring1][#Branch1][C][=Ring2][Ring1][#Branch2][C],\"2-(5,6-dimethylthieno[3,2-e]pyrimidin-4-yl)sulfanyl-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethanone\",2.7\nCN(C)CC(O)COc1ccc(Nc2ncc(Cl)c(Nc3ccccc3)n2)cc1,\"InChI=1S/C21H24ClN5O2/c1-27(2)13-17(28)14-29-18-10-8-16(9-11-18)25-21-23-12-19(22)20(26-21)24-15-6-4-3-5-7-15/h3-12,17,28H,13-14H2,1-2H3,(H2,23,24,25,26)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][Branch1][C][Cl][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1],1-[4-[[5-chloro-4-(phenylamino)pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol,2.25\nCCOC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])NC(=O)c2ccccc2,\"InChI=1S/C18H18N2O5/c1-2-25-18(22)16(19-17(21)14-6-4-3-5-7-14)12-13-8-10-15(11-9-13)20(23)24/h3-11,16H,2,12H2,1H3,(H,19,21)/t16-/m0/s1\",[C][C][O][C][=Branch1][C][=O][C@H1][Branch1][P][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],ethyl (2s)-2-(benzoylamino)-3-(4-nitrophenyl)propanoate,2.79\nC[C@]12CCC(=O)C=C1CC[C@H]3[C@@H]4CC[C@](O)(C(=O)CO)[C@@]4(C)CC(=O)[C@H]23,\"InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-15,18,22,26H,3-8,10-11H2,1-2H3/t14-,15-,18+,19-,20-,21-/m0/s1\",[C][C@][C][C][C][=Branch1][C][=O][C][=C][Ring1][#Branch1][C][C][C@H1][C@@H1][C][C][C@][Branch1][C][O][Branch1][#Branch1][C][=Branch1][C][=O][C][O][C@@][Ring1][#Branch2][Branch1][C][C][C][C][=Branch1][C][=O][C@H1][Ring2][Ring1][=Branch2][Ring1][S],\"(8s,9s,10r,13s,14s,17r)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11-dione\",1.4\nCN1C(=O)C=C(CCc2cccc(c2)c3ccccc3)N=C1N,\"InChI=1S/C19H19N3O/c1-22-18(23)13-17(21-19(22)20)11-10-14-6-5-9-16(12-14)15-7-3-2-4-8-15/h2-9,12-13H,10-11H2,1H3,(H2,20,21)\",[C][N][C][=Branch1][C][=O][C][=C][Branch2][Ring1][Branch1][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring2][Ring1][Branch1][N],2-amino-3-methyl-6-[2-(3-phenylphenyl)ethyl]pyrimidin-4-one,3.8\nCCCNCC(O)COc1ccccc1C(=O)CCc2ccccc2,\"InChI=1S/C21H27NO3/c1-2-14-22-15-18(23)16-25-21-11-7-6-10-19(21)20(24)13-12-17-8-4-3-5-9-17/h3-11,18,22-23H,2,12-16H2,1H3\",[C][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],1-[2-(2-hydroxy-3-propylaminopropoxy)phenyl]-3-phenylpropan-1-one,1.72\nCCN(CC)c1ccc2C=C(C(=O)O)C(=O)Oc2c1,\"InChI=1S/C14H15NO4/c1-3-15(4-2)10-6-5-9-7-11(13(16)17)14(18)19-12(9)8-10/h5-8H,3-4H2,1-2H3,(H,16,17)\",[C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][O][C][Ring1][#Branch2][=C][Ring1][=C],7-diethylamino-2-oxochromene-3-carboxylic acid,-0.2\nCCOC(=O)\\C=C\\[C@H](C[C@@H]1CCNC1=O)NC(=O)[C@@H](CC(=O)[C@@H](NC(=O)c2cc(C)on2)C(C)C)Cc3ccc(F)cc3,\"InChI=1S/C31H39FN4O7/c1-5-42-27(38)11-10-24(16-21-12-13-33-29(21)39)34-30(40)22(15-20-6-8-23(32)9-7-20)17-26(37)28(18(2)3)35-31(41)25-14-19(4)43-36-25/h6-11,14,18,21-22,24,28H,5,12-13,15-17H2,1-4H3,(H,33,39)(H,34,40)(H,35,41)/b11-10+/t21-,22+,24+,28-/m0/s1\",[C][C][O][C][=Branch1][C][=O][\\C][=C][\\C@H1][Branch1][#Branch2][C][C@@H1][C][C][N][C][Ring1][Branch1][=O][N][C][=Branch1][C][=O][C@@H1][Branch2][Ring1][=N][C][C][=Branch1][C][=O][C@@H1][Branch1][S][N][C][=Branch1][C][=O][C][C][=C][Branch1][C][C][O][N][=Ring1][=Branch1][C][Branch1][C][C][C][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"ethyl (e,4s)-4-[[(2r,5s)-2-[(4-fluorophenyl)methyl]-6-methyl-5-[(5-methyl1,2-oxazole-3-carbonyl)amino]-4-oxoheptanoyl]amino]-5-[(3s)-2-oxopyrrolidin-3-yl]pent-2-enoate\",2.8\nCN1N(C(=O)C=C1C)c2ccccc2,\"InChI=1S/C11H12N2O/c1-9-8-11(14)13(12(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3\",[C][N][N][Branch1][#Branch2][C][=Branch1][C][=O][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1,5-dimethyl-2-phenylpyrazol-3-one\",0.11\nCC(C)[C@H](N)C(=O)OCCOCn1cnc2C(=O)N=C(N)Nc12,\"InChI=1S/C13H20N6O4/c1-7(2)8(14)12(21)23-4-3-22-6-19-5-16-9-10(19)17-13(15)18-11(9)20/h5,7-8H,3-4,6,14H2,1-2H3,(H3,15,17,18,20)/t8-/m0/s1\",[C][C][Branch1][C][C][C@H1][Branch1][C][N][C][=Branch1][C][=O][O][C][C][O][C][N][C][=N][C][C][=Branch1][C][=O][N][=C][Branch1][C][N][N][C][Ring1][O][=Ring1][Branch2],2-[(2-amino-6-oxo-3h-purin-9-yl)methoxy]ethyl (2s)-2-amino-3-methylbutanoate,-1.3\nClc1ccc(CN2C[C@@H]3C[C@H]2CN3)cc1C(=O)NCC45CC6CC(CC(C6)C4)C5,\"InChI=1S/C24H32ClN3O/c25-22-2-1-15(12-28-13-19-7-20(28)11-26-19)6-21(22)23(29)27-14-24-8-16-3-17(9-24)5-18(4-16)10-24/h1-2,6,16-20,26H,3-5,7-14H2,(H,27,29)/t16?,17?,18?,19-,20-,24?/m0/s1\",[Cl][C][=C][C][=C][Branch1][=N][C][N][C][C@@H1][C][C@H1][Ring1][Branch1][C][N][Ring1][Branch1][C][=C][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],\"n-(1-adamantylmethyl)-2-chloro-5-[[(1s,4s)-3,6-diazabicyclo[2.2.1]heptan-6-yl]methyl]benzamide\",1.45\nCC(=O)Nc1nc(N)n(n1)c2ccccc2,\"InChI=1S/C10H11N5O/c1-7(16)12-10-13-9(11)15(14-10)8-5-3-2-4-6-8/h2-6H,1H3,(H3,11,12,13,14,16)\",[C][C][=Branch1][C][=O][N][C][N][=C][Branch1][C][N][N][Branch1][Ring2][N][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-(5-amino-1-phenyl-1,2,4-triazol-3-yl)acetamide\",-0.2\nCC(C)NC[C@H](O)COc1cccc2ccccc12,\"InChI=1S/C16H21NO2/c1-12(2)17-10-14(18)11-19-16-9-5-7-13-6-3-4-8-15(13)16/h3-9,12,14,17-18H,10-11H2,1-2H3/t14-/m0/s1\",[C][C][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],(2s)-1-naphthalen-1-yloxy-3-(propan-2-ylamino)propan-2-ol,0.99\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)Cc3ccccc3C(=O)O)C(=O)C(F)(F)F,\"InChI=1S/C28H26F3N3O6/c1-16(2)24(25(37)28(29,30)31)33-23(36)15-34-21(17-8-4-3-5-9-17)13-12-20(26(34)38)32-22(35)14-18-10-6-7-11-19(18)27(39)40/h3-13,16,24H,14-15H2,1-2H3,(H,32,35)(H,33,36)(H,39,40)\",[C][C][Branch1][C][C][C][Branch2][Ring2][#C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-2-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]amino]ethyl]benzoic acid\",1.14\nCCN(CC)c1ccc2C=C(C(=O)C)C(=O)Oc2c1,\"InChI=1S/C15H17NO3/c1-4-16(5-2)12-7-6-11-8-13(10(3)17)15(18)19-14(11)9-12/h6-9H,4-5H2,1-3H3\",[C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=Branch1][C][=O][O][C][Ring1][#Branch2][=C][Ring1][=C],3-acetyl-7-diethylaminochromen-2-one,2\nCCOC(=O)c1c(nc2cc(C)ccn12)c3ccccc3,\"InChI=1S/C17H16N2O2/c1-3-21-17(20)16-15(13-7-5-4-6-8-13)18-14-11-12(2)9-10-19(14)16/h4-11H,3H2,1-2H3\",[C][C][O][C][=Branch1][C][=O][C][=C][Branch1][#C][N][=C][C][=C][Branch1][C][C][C][=C][N][Ring1][#Branch2][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"ethyl 7-methyl-2-phenylimidazo[3,2-a]pyridine-3-carboxylate\",3.8\nCCN(CC)CCOC(=O)c1ccc(N)cc1,\"InChI=1S/C13H20N2O2/c1-3-15(4-2)9-10-17-13(16)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10,14H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],2-diethylaminoethyl 4-aminobenzoate,0\nNC(Cc1cc(I)c(Oc2ccc(O)c(I)c2)c(I)c1)C(=O)O,\"InChI=1S/C15H12I3NO4/c16-9-6-8(1-2-13(9)20)23-14-10(17)3-7(4-11(14)18)5-12(19)15(21)22/h1-4,6,12,20H,5,19H2,(H,21,22)\",[N][C][Branch2][Ring1][P][C][C][=C][C][Branch1][C][I][=C][Branch1][S][O][C][=C][C][=C][Branch1][C][O][C][Branch1][C][I][=C][Ring1][Branch2][C][Branch1][C][I][=C][Ring1][P][C][=Branch1][C][=O][O],\"2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid\",0.97\nO=C1C(=O)c2ccccc2c3ccccc13,InChI=1S/C14H8O2/c15-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(13)16/h1-8H,[O][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"phenanthrene-9,10-dione\",2.6\nClc1ccc(CN2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C23H32ClN3O/c24-21-2-1-16(14-27-5-3-25-4-6-27)10-20(21)22(28)26-15-23-11-17-7-18(12-23)9-19(8-17)13-23/h1-2,10,17-19,25H,3-9,11-15H2,(H,26,28)\",[Cl][C][=C][C][=C][Branch1][#Branch2][C][N][C][C][N][C][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chloro-5-(piperazin-1-ylmethyl)benzamide,1.84\nFc1ccc(cc1)n2cc(C3CCNCC3)c4cc(Cl)ccc24,\"InChI=1S/C19H18ClFN2/c20-14-1-6-19-17(11-14)18(13-7-9-22-10-8-13)12-23(19)16-4-2-15(21)3-5-16/h1-6,11-13,22H,7-10H2\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=C][Branch1][=Branch2][C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][S][Ring1][#Branch1],5-chloro-1-(4-fluorophenyl)-3-piperidin-4-ylindole,2.4\nCOC(=O)NC1=CN=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccc(F)cc2,\"InChI=1S/C20H20F4N4O5/c1-10(2)15(16(30)20(22,23)24)27-14(29)9-28-17(11-4-6-12(21)7-5-11)25-8-13(18(28)31)26-19(32)33-3/h4-8,10,15H,9H2,1-3H3,(H,26,32)(H,27,29)\",[C][O][C][=Branch1][C][=O][N][C][=C][N][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"methyl n-[2-(4-fluorophenyl)-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\",1.82\nCC(N)C(=O)Nc1c(C)cccc1C,\"InChI=1S/C11H16N2O/c1-7-5-4-6-8(2)10(7)13-11(14)9(3)12/h4-6,9H,12H2,1-3H3,(H,13,14)\",[C][C][Branch1][C][N][C][=Branch1][C][=O][N][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C],\"2-amino-n-(2,6-dimethylphenyl)propanamide\",-0.15\nNC1CCN(CC1)c2nccc(C(=O)NCC34CC5CC(CC(C5)C3)C4)c2Cl,\"InChI=1S/C22H31ClN4O/c23-19-18(1-4-25-20(19)27-5-2-17(24)3-6-27)21(28)26-13-22-10-14-7-15(11-22)9-16(8-14)12-22/h1,4,14-17H,2-3,5-13,24H2,(H,26,28)\",[N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][Cl],n-(1-adamantylmethyl)-2-(4-aminopiperidin-1-yl)-3-chloropyridine-4-carboxamide,1.19\nCOc1ccc(cc1)C(=O)N2CCC(CC2)C(=O)c3ccc(F)cc3,\"InChI=1S/C20H20FNO3/c1-25-18-8-4-16(5-9-18)20(24)22-12-10-15(11-13-22)19(23)14-2-6-17(21)7-3-14/h2-9,15H,10-13H2,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],(4-fluorophenyl)-[1-(4-methoxybenzoyl)piperidin-4-yl]methanone,2.92\nCc1ccc(OC(=O)N2CCN3CCC2CC3)cc1,\"InChI=1S/C15H20N2O2/c1-12-2-4-14(5-3-12)19-15(18)17-11-10-16-8-6-13(17)7-9-16/h2-5,13H,6-11H2,1H3\",[C][C][=C][C][=C][Branch2][Ring1][Ring1][O][C][=Branch1][C][=O][N][C][C][N][C][C][C][Ring1][#Branch1][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][C],\"(4-methylphenyl) 1,4-diazabicyclo[3.2.2]nonane-4-carboxylate\",1.02\nCCN(CC)C(=O)c1ccc(C2=CC3(CCNCC3)Oc4ccccc24)c(O)c1,\"InChI=1S/C24H28N2O3/c1-3-26(4-2)23(28)17-9-10-18(21(27)15-17)20-16-24(11-13-25-14-12-24)29-22-8-6-5-7-19(20)22/h5-10,15-16,25,27H,3-4,11-14H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch2][C][=C][C][Branch1][Branch2][C][C][N][C][C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1][C][Branch1][C][O][=C][Ring2][Ring1][=Branch1],\"n,n-diethyl-3-hydroxy-4-spiro[chromene-2,4'-piperidine]-4-ylbenzamide\",0.77\nCCOC(=O)CN(c1ccccc1C)S(=O)(=O)c2ccc(Cl)cc2,\"InChI=1S/C17H18ClNO4S/c1-3-23-17(20)12-19(16-7-5-4-6-13(16)2)24(21,22)15-10-8-14(18)9-11-15/h4-11H,3,12H2,1-2H3\",[C][C][O][C][=Branch1][C][=O][C][N][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],ethyl 2-[(4-chlorophenyl)sulfonyl-(2-methylphenyl)amino]acetate,4.03\n[O-][n+]1cc(ccc1Cl)C(=O)Nc2ccc(F)cc2,\"InChI=1S/C12H8ClFN2O2/c13-11-6-1-8(7-16(11)18)12(17)15-10-4-2-9(14)3-5-10/h1-7H,(H,15,17)\",[O-1][N+1][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],6-chloro-n-(4-fluorophenyl)-1-oxidopyridin-1-ium-3-carboxamide,1.38\nCn1nc(cc1NC(=O)Nc2ccc(Cl)cc2)C(C)(C)C,\"InChI=1S/C15H19ClN4O/c1-15(2,3)12-9-13(20(4)19-12)18-14(21)17-11-7-5-10(16)6-8-11/h5-9H,1-4H3,(H2,17,18,21)\",[C][N][N][=C][Branch2][Ring1][=Branch1][C][=C][Ring1][Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][C][Branch1][C][C][C],1-(5-tert-butyl-2-methylpyrazol-3-yl)-3-(4-chlorophenyl)urea,3.97\nCC1Nc2cc(Cl)c(cc2C(=O)N1c3ccccc3C)S(=O)(=O)N,\"InChI=1S/C16H16ClN3O3S/c1-9-5-3-4-6-14(9)20-10(2)19-13-8-12(17)15(24(18,22)23)7-11(13)16(20)21/h3-8,10,19H,1-2H3,(H2,18,22,23)\",[C][C][N][C][=C][C][Branch1][C][Cl][=C][Branch2][Ring1][Branch1][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][N],\"7-chloro-2-methyl-3-(2-methylphenyl)-4-oxo-1,2-dihydroquinazoline-6-sulfonamide\",1.64\nCNC(=O)c1cc(C(=O)c2ccc(Cl)cc2)c(Br)[nH]1,\"InChI=1S/C13H10BrClN2O2/c1-16-13(19)10-6-9(12(14)17-10)11(18)7-2-4-8(15)5-3-7/h2-6,17H,1H3,(H,16,19)\",[C][N][C][=Branch1][C][=O][C][=C][C][Branch1][S][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][Br][NH1][Ring1][#C],5-bromo-4-(4-chlorobenzoyl)-n-methyl-1h-pyrrole-2-carboxamide,3.1\nCc1ccc(cc1)S(=O)(=O)c2ccccc2,\"InChI=1S/C13H12O2S/c1-11-7-9-13(10-8-11)16(14,15)12-5-3-2-4-6-12/h2-10H,1H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],1-methyl-4-phenylsulfonylbenzene,2.74\nCOc1ccc(Sc2c(C)n(CC(=O)O)c3ccc(C)cc23)cc1,\"InChI=1S/C19H19NO3S/c1-12-4-9-17-16(10-12)19(13(2)20(17)11-18(21)22)24-15-7-5-14(23-3)6-8-15/h4-10H,11H2,1-3H3,(H,21,22)\",[C][O][C][=C][C][=C][Branch2][Ring1][=N][S][C][=C][Branch1][C][C][N][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch1],\"2-[3-(4-methoxyphenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\",1.01\nCc1ccc2c(c1)c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O,\"InChI=1S/C18H16ClNO2S/c1-11-3-8-16-15(9-11)18(12(2)20(16)10-17(21)22)23-14-6-4-13(19)5-7-14/h3-9H,10H2,1-2H3,(H,21,22)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O],\"2-[3-(4-chlorophenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\",2.18\nClc1cccc(NC(=O)c2ccccn2)c1,\"InChI=1S/C12H9ClN2O/c13-9-4-3-5-10(8-9)15-12(16)11-6-1-2-7-14-11/h1-8H,(H,15,16)\",[Cl][C][=C][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring1][#C],n-(3-chlorophenyl)pyridine-2-carboxamide,3.4\nO=C1NC=Nc2scc(c3cccs3)c12,\"InChI=1S/C10H6N2OS2/c13-9-8-6(7-2-1-3-14-7)4-15-10(8)12-5-11-9/h1-5H,(H,11,12,13)\",[O][=C][N][C][=N][C][S][C][=C][Branch1][Branch2][C][=C][C][=C][S][Ring1][Branch1][C][Ring1][=C][=Ring1][#Branch2],\"5-thiophen-2-yl-3h-thieno[3,2-e]pyrimidin-4-one\",2.18\nOCCN1CCN(CCCN2c3ccccc3Sc4ccc(Cl)cc24)CC1,\"InChI=1S/C21H26ClN3OS/c22-17-6-7-21-19(16-17)25(18-4-1-2-5-20(18)27-21)9-3-8-23-10-12-24(13-11-23)14-15-26/h1-2,4-7,16,26H,3,8-15H2\",[O][C][C][N][C][C][N][Branch2][Ring1][O][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1][C][C][Ring2][Ring1][Branch2],2-[4-[3-(2-chlorophenothiazin-10-yl)propyl]piperazin-1-yl]ethanol,3.6\nNc1ccccc1NC(=O)c2ccc(cc2)c3nccs3,\"InChI=1S/C16H13N3OS/c17-13-3-1-2-4-14(13)19-15(20)11-5-7-12(8-6-11)16-18-9-10-21-16/h1-10H,17H2,(H,19,20)\",[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][S][Ring1][Branch1],\"n-(2-aminophenyl)-4-(1,3-thiazol-2-yl)benzamide\",2.3\nNc1ncc([nH]1)c2ccc(F)cc2,\"InChI=1S/C9H8FN3/c10-7-3-1-6(2-4-7)8-5-12-9(11)13-8/h1-5H,(H3,11,12,13)\",[N][C][=N][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],4-(4-fluorophenyl)-3h-imidazol-2-amine,1.39\nClc1cc(Nc2ncnc3[nH]nc(OCCN4CCCC4)c23)ccc1OCc5ccccn5,\"InChI=1S/C23H24ClN7O2/c24-18-13-16(6-7-19(18)33-14-17-5-1-2-8-25-17)28-21-20-22(27-15-26-21)29-30-23(20)32-12-11-31-9-3-4-10-31/h1-2,5-8,13,15H,3-4,9-12,14H2,(H2,26,27,28,29,30)\",[Cl][C][=C][C][Branch2][Ring1][O][N][C][=N][C][=N][C][NH1][N][=C][Branch1][O][O][C][C][N][C][C][C][C][Ring1][Branch1][C][Ring1][P][=Ring1][=N][=C][C][=C][Ring2][Ring1][Branch2][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1],\"n-[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]-3-(2-pyrrolidin-1-ylethoxy)-1h-pyrazolo[4,5-e]pyrimidin-4-amine\",2.87\nCOc1ccc(cc1)c2ccnc(N)n2,\"InChI=1S/C11H11N3O/c1-15-9-4-2-8(3-5-9)10-6-7-13-11(12)14-10/h2-7H,1H3,(H2,12,13,14)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][C][N][=N][Ring1][#Branch1],4-(4-methoxyphenyl)pyrimidin-2-amine,2.08\nNC(=O)NC(=O)C(Nc1ccc2CCCc2c1)c3ccccc3,\"InChI=1S/C18H19N3O2/c19-18(23)21-17(22)16(13-5-2-1-3-6-13)20-15-10-9-12-7-4-8-14(12)11-15/h1-3,5-6,9-11,16,20H,4,7-8H2,(H3,19,21,22,23)\",[N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Branch1][#C][N][C][=C][C][=C][C][C][C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-carbamoyl-2-(2,3-dihydro-1h-inden-5-ylamino)-2-phenylacetamide\",3.3\nCCCSc1ccc2nc(NC(=O)OC)[nH]c2c1,\"InChI=1S/C12H15N3O2S/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)\",[C][C][C][S][C][=C][C][=C][N][=C][Branch1][Branch2][N][C][=Branch1][C][=O][O][C][NH1][C][Ring1][#Branch2][=C][Ring1][=C],methyl n-(6-propylsulfanyl-1h-benzimidazol-2-yl)carbamate,3.24\nCCOc1ccc2nc(N)sc2c1,\"InChI=1S/C9H10N2OS/c1-2-12-6-3-4-7-8(5-6)13-9(10)11-7/h3-5H,2H2,1H3,(H2,10,11)\",[C][C][O][C][=C][C][=C][N][=C][Branch1][C][N][S][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"6-ethoxy-1,3-benzothiazol-2-amine\",2.4\nN(c1ccccc1)c2ccnc3ccccc23,\"InChI=1S/C15H12N2/c1-2-6-12(7-3-1)17-15-10-11-16-14-9-5-4-8-13(14)15/h1-11H,(H,16,17)\",[N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],n-phenylquinolin-4-amine,2.78\nCOc1cc(ccc1Cn2ccc3ccc(cc23)C(=O)NCC4CCCC4)C(=O)NS(=O)(=O)c5ccccc5,\"InChI=1S/C30H31N3O5S/c1-38-28-18-24(30(35)32-39(36,37)26-9-3-2-4-10-26)13-14-25(28)20-33-16-15-22-11-12-23(17-27(22)33)29(34)31-19-21-7-5-6-8-21/h2-4,9-18,21H,5-8,19-20H2,1H3,(H,31,34)(H,32,35)\",[C][O][C][=C][C][=Branch2][Ring2][Ring1][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],n-(cyclopentylmethyl)-1-[[2-methoxy-4-(phenylsulfonylcarbamoyl)phenyl]methyl]indole-6-carboxamide,1.93\nNC1=NN(CC1)c2cccc(c2)C(F)(F)F,\"InChI=1S/C10H10F3N3/c11-10(12,13)7-2-1-3-8(6-7)16-5-4-9(14)15-16/h1-3,6H,4-5H2,(H2,14,15)\",[N][C][=N][N][Branch1][Branch1][C][C][Ring1][Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"1-[3-(trifluoromethyl)phenyl]-4,5-dihydropyrazol-3-amine\",2.55\nCC(C)(C(=O)Nc1oc(nn1)C(=O)Nc2ccc(cc2)N3CCOCC3)c4ccc(Cl)cc4,\"InChI=1S/C23H24ClN5O4/c1-23(2,15-3-5-16(24)6-4-15)21(31)26-22-28-27-20(33-22)19(30)25-17-7-9-18(10-8-17)29-11-13-32-14-12-29/h3-10H,11-14H2,1-2H3,(H,25,30)(H,26,28,31)\",[C][C][Branch1][C][C][Branch2][Ring2][=Branch1][C][=Branch1][C][=O][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"5-[[2-(4-chlorophenyl)-2-methylpropanoyl]amino]-n-(4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\",2.96\nCc1ccc(cc1)C(=O)N2CCC(CC2)C(=O)c3ccc(Cl)cc3,\"InChI=1S/C20H20ClNO2/c1-14-2-4-17(5-3-14)20(24)22-12-10-16(11-13-22)19(23)15-6-8-18(21)9-7-15/h2-9,16H,10-13H2,1H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],(4-chlorophenyl)-[1-(4-methylbenzoyl)piperidin-4-yl]methanone,3.79\nc1ccc(nc1)c2nc3ccccc3[nH]2,\"InChI=1S/C12H9N3/c1-2-6-10-9(5-1)14-12(15-10)11-7-3-4-8-13-11/h1-8H,(H,14,15)\",[C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],2-pyridin-2-yl-1h-benzimidazole,2.5\n[O-][N+](=O)c1cc(ccc1NCCSc2ccccc2)S(=O)(=O)NC(=O)c3ccc(cc3)N4CCNCC4,\"InChI=1S/C25H27N5O5S2/c31-25(19-6-8-20(9-7-19)29-15-12-26-13-16-29)28-37(34,35)22-10-11-23(24(18-22)30(32)33)27-14-17-36-21-4-2-1-3-5-21/h1-11,18,26-27H,12-17H2,(H,28,31)\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=Branch2][Ring1][C][=C][C][=C][Ring1][=Branch1][N][C][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][C][C][Ring1][=Branch1],n-[3-nitro-4-(2-phenylsulfanylethylamino)phenyl]sulfonyl-4-piperazin-1-ylbenzamide,-0.04\nNc1cc(nc2ccc(Nc3cc(nc(N)n3)c4ccc(cc4)C(F)(F)F)cc12)c5ccc(F)cc5,\"InChI=1S/C26H18F4N6/c27-17-7-3-15(4-8-17)22-12-20(31)19-11-18(9-10-21(19)34-22)33-24-13-23(35-25(32)36-24)14-1-5-16(6-2-14)26(28,29)30/h1-13H,(H2,31,34)(H3,32,33,35,36)\",[N][C][=C][C][=Branch2][Ring2][P][=N][C][=C][C][=C][Branch2][Ring1][P][N][C][=C][C][=Branch1][=Branch2][=N][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring2][Ring1][N][Ring2][Ring1][Branch2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"n'-[2-amino-6-[4-(trifluoromethyl)phenyl]pyrimidin-4-yl]-2-(4-fluorophenyl)quinoline-4,6-diamine\",1.54\nFc1cnc(NC(=O)[C@H](CC2CCOCC2)c3ccc(cc3)S(=O)(=O)C4CC4)s1,\"InChI=1S/C20H23FN2O4S2/c21-18-12-22-20(28-18)23-19(24)17(11-13-7-9-27-10-8-13)14-1-3-15(4-2-14)29(25,26)16-5-6-16/h1-4,12-13,16-17H,5-11H2,(H,22,23,24)/t17-/m1/s1\",[F][C][=C][N][=C][Branch2][Ring2][Branch2][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring1][Ring1][S][Ring2][Ring1][N],\"(2r)-2-(4-cyclopropylsulfonylphenyl)-n-(5-fluoro-1,3-thiazol-2-yl)-3-(oxan-4-yl)propanamide\",3.19\nNC(=N)SCc1ccc(Cl)c(Cl)c1,\"InChI=1S/C8H8Cl2N2S/c9-6-2-1-5(3-7(6)10)4-13-8(11)12/h1-3H,4H2,(H3,11,12)\",[N][C][=Branch1][C][=N][S][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"(3,4-dichlorophenyl)methylsulfanylmethanimidamide\",1.28\nCc1ccc(COC(=O)N2CCC(CNc3ncccn3)CC2)cc1,\"InChI=1S/C19H24N4O2/c1-15-3-5-17(6-4-15)14-25-19(24)23-11-7-16(8-12-23)13-22-18-20-9-2-10-21-18/h2-6,9-10,16H,7-8,11-14H2,1H3,(H,20,21,22)\",[C][C][=C][C][=C][Branch2][Ring1][O][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][O][C][N][C][=N][C][=C][C][=N][Ring1][=Branch1][C][C][Ring1][=C][C][=C][Ring2][Ring1][Branch2],(4-methylphenyl)methyl 4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate,3.6\nCOC[C@H](C)Oc1cc(O[C@@H](C)Cc2ccccc2)cc(c1)C(=O)Nc3ccc(cn3)C(=O)O,\"InChI=1S/C26H28N2O6/c1-17(11-19-7-5-4-6-8-19)33-22-12-21(13-23(14-22)34-18(2)16-32-3)25(29)28-24-10-9-20(15-27-24)26(30)31/h4-10,12-15,17-18H,11,16H2,1-3H3,(H,30,31)(H,27,28,29)/t17-,18-/m0/s1\",[C][O][C][C@H1][Branch1][C][C][O][C][=C][C][Branch1][#C][O][C@@H1][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Ring2][=C][Ring1][S][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O],6-[[3-[(2s)-1-methoxypropan-2-yl]oxy-5-[(2s)-1-phenylpropan-2-yl]oxybenzoyl]amino]pyridine-3-carboxylic acid,1.5\nCOc1cc(ccc1Nc2ccccc2C(=O)O)c3ccc(Nc4ccccc4C(=O)O)c(OC)c3,\"InChI=1S/C28H24N2O6/c1-35-25-15-17(11-13-23(25)29-21-9-5-3-7-19(21)27(31)32)18-12-14-24(26(16-18)36-2)30-22-10-6-4-8-20(22)28(33)34/h3-16,29-30H,1-2H3,(H,31,32)(H,33,34)\",[C][O][C][=C][C][=Branch2][Ring1][Ring2][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][#C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][C],2-[[4-[4-[(2-carboxyphenyl)amino]-3-methoxyphenyl]-2-methoxyphenyl]amino]benzoic acid,1.8\nCOc1cc(cc(OC)c1OC)C(=O)c2cc(Cl)ccc2N,\"InChI=1S/C16H16ClNO4/c1-20-13-6-9(7-14(21-2)16(13)22-3)15(19)11-8-10(17)4-5-12(11)18/h4-8H,18H2,1-3H3\",[C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N],\"(2-amino-5-chlorophenyl)-(3,4,5-trimethoxyphenyl)methanone\",3.38\nCN(C)CC1CCn2c(C1)c(C3=C(C(=O)NC3=O)c4cn(C)c5ccccc45)c6ccccc26,\"InChI=1S/C28H28N4O2/c1-30(2)15-17-12-13-32-22-11-7-5-9-19(22)24(23(32)14-17)26-25(27(33)29-28(26)34)20-16-31(3)21-10-6-4-8-18(20)21/h4-11,16-17H,12-15H2,1-3H3,(H,29,33,34)\",[C][N][Branch1][C][C][C][C][C][C][N][C][Branch1][Ring2][C][Ring1][=Branch1][=C][Branch2][Ring1][=C][C][=C][Branch1][#Branch2][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=O][C][=C][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][O][Ring1][=Branch1],\"3-[8-(dimethylaminomethyl)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione\",2.88\nCOc1ccc2cc(CCC(=O)C)ccc2c1,\"InChI=1S/C15H16O2/c1-11(16)3-4-12-5-6-14-10-15(17-2)8-7-13(14)9-12/h5-10H,3-4H2,1-2H3\",[C][O][C][=C][C][=C][C][=C][Branch1][Branch2][C][C][C][=Branch1][C][=O][C][C][=C][C][Ring1][O][=C][Ring1][#C],4-(6-methoxynaphthalen-2-yl)butan-2-one,3.06\nOc1ccc(NC(=O)c2ccc(O)cc2)cc1,\"InChI=1S/C13H11NO3/c15-11-5-1-9(2-6-11)13(17)14-10-3-7-12(16)8-4-10/h1-8,15-16H,(H,14,17)\",[O][C][=C][C][=C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][Ring1][S],4-hydroxy-n-(4-hydroxyphenyl)benzamide,1.5\nCOC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])NC(=O)c2cccc3ccccc23,\"InChI=1S/C21H18N2O5/c1-28-21(25)19(13-14-9-11-16(12-10-14)23(26)27)22-20(24)18-8-4-6-15-5-2-3-7-17(15)18/h2-12,19H,13H2,1H3,(H,22,24)/t19-/m0/s1\",[C][O][C][=Branch1][C][=O][C@H1][Branch1][P][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],methyl (2s)-2-(naphthalene-1-carbonylamino)-3-(4-nitrophenyl)propanoate,3.58\nCC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)C(=O)N)n2,\"InChI=1S/C18H20N6O/c1-11(2)24-12(3)21-10-16(24)15-8-9-20-18(23-15)22-14-6-4-13(5-7-14)17(19)25/h4-11H,1-3H3,(H2,19,25)(H,20,22,23)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][P][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][=N][Ring1][S],4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide,2.39\nCc1ccc(OCC(=O)O)c(c1)n2nc3ccccc3n2,\"InChI=1S/C15H13N3O3/c1-10-6-7-14(21-9-15(19)20)13(8-10)18-16-11-4-2-3-5-12(11)17-18/h2-8H,9H2,1H3,(H,19,20)\",[C][C][=C][C][=C][Branch1][Branch2][O][C][C][=Branch1][C][=O][O][C][=Branch1][Ring2][=C][Ring1][O][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2],2-[2-(benzotriazol-2-yl)-4-methylphenoxy]acetic acid,-0.84\nFc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1,\"InChI=1S/C23H26FN5O4/c24-15-1-3-19-18(11-15)29(22(31)14-33-19)10-9-28-7-5-16(6-8-28)25-12-17-2-4-20-23(26-17)27-21(30)13-32-20/h1-4,11,16,25H,5-10,12-14H2,(H,26,27,30)\",[F][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S],\"6-[[[1-[2-(6-fluoro-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",0.9\nN(c1ccccc1)c2ccccc2,\"InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H\",[N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-phenylaniline,3.2\nOc1cccc2ccccc12,\"InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H\",[O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],naphthalen-1-ol,2.5\nCCN1CCN(CC1)C(=O)c2cc3cc(Cl)ccc3[nH]2,\"InChI=1S/C15H18ClN3O/c1-2-18-5-7-19(8-6-18)15(20)14-10-11-9-12(16)3-4-13(11)17-14/h3-4,9-10,17H,2,5-8H2,1H3\",[C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],(5-chloro-1h-indol-2-yl)-(4-ethylpiperazin-1-yl)methanone,3.14\nCOc1ccc2c(c1)cc(C(=O)O)n2Cc3ccc(Cl)c(Cl)c3,\"InChI=1S/C17H13Cl2NO3/c1-23-12-3-5-15-11(7-12)8-16(17(21)22)20(15)9-10-2-4-13(18)14(19)6-10/h2-8H,9H2,1H3,(H,21,22)\",[C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][N][Ring1][=Branch2][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"1-[(3,4-dichlorophenyl)methyl]-5-methoxyindole-2-carboxylic acid\",1.66\nC[C@H](N)C(=O)N[C@@H](CCc1ccccc1)\\C=C\\S(=O)(=O)c2ccccc2,\"InChI=1S/C20H24N2O3S/c1-16(21)20(23)22-18(13-12-17-8-4-2-5-9-17)14-15-26(24,25)19-10-6-3-7-11-19/h2-11,14-16,18H,12-13,21H2,1H3,(H,22,23)/b15-14+/t16-,18-/m0/s1\",[C][C@H1][Branch1][C][N][C][=Branch1][C][=O][N][C@@H1][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][\\C][=C][\\S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(2s)-2-amino-n-[(e,3s)-5-phenyl-1-phenylsulfonylpent-1-en-3-yl]propanamide\",1.66\nOC(c1ccc(cc1)N(CC(F)(F)F)S(=O)(=O)c2ccccc2)(C(F)(F)F)C(F)(F)F,\"InChI=1S/C17H12F9NO3S/c18-14(19,20)10-27(31(29,30)13-4-2-1-3-5-13)12-8-6-11(7-9-12)15(28,16(21,22)23)17(24,25)26/h1-9,28H,10H2\",[O][C][Branch2][Ring2][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][#Branch2][C][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][Branch1][=Branch2][C][Branch1][C][F][Branch1][C][F][F][C][Branch1][C][F][Branch1][C][F][F],\"n-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-n-(2,2,2-trifluoroethyl)benzenesulfonamide\",4.5\nCCN(CC)CCNC(=O)c1ccc(N)cc1,\"InChI=1S/C13H21N3O/c1-3-16(4-2)10-9-15-13(17)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10,14H2,1-2H3,(H,15,17)\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],4-amino-n-(2-diethylaminoethyl)benzamide,-0.92\nO=C(Nc1ccc(Nc2ccc(NC(=O)c3ccccc3)c4C(=O)c5ccccc5C(=O)c24)c6C(=O)c7ccccc7C(=O)c16)c8ccccc8,\"InChI=1S/C42H25N3O6/c46-37-25-15-7-9-17-27(25)39(48)35-31(44-41(50)23-11-3-1-4-12-23)21-19-29(33(35)37)43-30-20-22-32(45-42(51)24-13-5-2-6-14-24)36-34(30)38(47)26-16-8-10-18-28(26)40(36)49/h1-22,43H,(H,44,50)(H,45,51)\",[O][=C][Branch2][=Branch1][O][N][C][=C][C][=C][Branch2][Ring2][N][N][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring2][Ring1][=Branch2][=Ring1][N][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring2][Ring2][#Branch2][=Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-[4-[[4-(benzoylamino)-9,10-dioxoanthracen-1-yl]amino]-9,10-dioxoanthracen-1-yl]benzamide\",2.63\nCOc1ccccc1CN[C@H]2CCCN[C@H]2c3ccccc3,\"InChI=1S/C19H24N2O/c1-22-18-12-6-5-10-16(18)14-21-17-11-7-13-20-19(17)15-8-3-2-4-9-15/h2-6,8-10,12,17,19-21H,7,11,13-14H2,1H3/t17-,19-/m0/s1\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C@H1][C][C][C][N][C@H1][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(2s,3s)-n-[(2-methoxyphenyl)methyl]-2-phenylpiperidin-3-amine\",1.5\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3cc(C)nc(C)c3)C(=O)C(F)(F)F,\"InChI=1S/C28H29F3N4O5/c1-16(2)24(25(37)28(29,30)31)34-23(36)14-35-22(20-8-6-5-7-9-20)11-10-21(26(35)38)33-27(39)40-15-19-12-17(3)32-18(4)13-19/h5-13,16,24H,14-15H2,1-4H3,(H,33,39)(H,34,36)\",[C][C][Branch1][C][C][C][Branch2][Ring2][P][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][Branch1][C][C][=N][C][Branch1][C][C][=C][Ring1][Branch2][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"(2,6-dimethylpyridin-4-yl)methyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamate\",2.38\nCOCCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1,\"InChI=1S/C21H22N6O3S/c1-30-14-4-11-24-31(28,29)17-8-6-16(7-9-17)25-21-22-12-10-18(26-21)19-15-23-20-5-2-3-13-27(19)20/h2-3,5-10,12-13,15,24H,4,11,14H2,1H3,(H,22,25,26)\",[C][O][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]-n-(3-methoxypropyl)benzenesulfonamide\",3.41\nCN[C@@H](C)[C@H](O)c1ccccc1,\"InChI=1S/C10H15NO/c1-8(11-2)10(12)9-6-4-3-5-7-9/h3-8,10-12H,1-2H3/t8-,10-/m0/s1\",[C][N][C@@H1][Branch1][C][C][C@H1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(1r,2s)-2-methylamino-1-phenylpropan-1-ol\",-1.15\nCOc1nc(N)nc2c1ncn2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O,\"InChI=1S/C11H15N5O5/c1-20-9-5-8(14-11(12)15-9)16(3-13-5)10-7(19)6(18)4(2-17)21-10/h3-4,6-7,10,17-19H,2H2,1H3,(H2,12,14,15)/t4-,6-,7-,10-/m1/s1\",[C][O][C][=N][C][Branch1][C][N][=N][C][=C][Ring1][#Branch1][N][=C][N][Ring1][Branch1][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O],\"(2r,3r,4s,5r)-2-(2-amino-6-methoxypurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol\",-0.58\nC[C@@H]1NC(C)(C)CO[C@@]1(O)c2cccc(Cl)c2,\"InChI=1S/C13H18ClNO2/c1-9-13(16,17-8-12(2,3)15-9)10-5-4-6-11(14)7-10/h4-7,9,15-16H,8H2,1-3H3/t9-,13+/m0/s1\",[C][C@@H1][N][C][Branch1][C][C][Branch1][C][C][C][O][C@@][Ring1][Branch2][Branch1][C][O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],\"(2s,3s)-2-(3-chlorophenyl)-3,5,5-trimethylmorpholin-2-ol\",1.69\nCCN(C1CCN(CCC(N2CCN(CC2)c3ccccc3)c4ccccc4)CC1)C(=O)Cc5ccc(cc5)S(=O)(=O)C,\"InChI=1S/C35H46N4O3S/c1-3-39(35(40)28-29-14-16-33(17-15-29)43(2,41)42)32-18-21-36(22-19-32)23-20-34(30-10-6-4-7-11-30)38-26-24-37(25-27-38)31-12-8-5-9-13-31/h4-17,32,34H,3,18-28H2,1-2H3\",[C][C][N][Branch2][Ring2][=N][C][C][C][N][Branch2][Ring1][P][C][C][C][Branch2][Ring1][Ring1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][O][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[3-phenyl-3-(4-phenylpiperazin-1-yl)propyl]piperidin-4-yl]acetamide,2.67\nCOC(=O)COc1ccc(O)cc1,\"InChI=1S/C9H10O4/c1-12-9(11)6-13-8-4-2-7(10)3-5-8/h2-5,10H,6H2,1H3\",[C][O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],methyl 2-(4-hydroxyphenoxy)acetate,0.92\nC(=C\\c1nn[nH]n1)/c2ccccc2,\"InChI=1S/C9H8N4/c1-2-4-8(5-3-1)6-7-9-10-12-13-11-9/h1-7H,(H,10,11,12,13)/b7-6+\",[C][=Branch1][=Branch2][=C][\\C][N][=N][NH1][N][=Ring1][Branch1][/C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-(2-phenylethenyl)-2h-tetrazole\n5-[(e)-2-phenylethenyl]-2h-tetrazole\",-0.4\nCOc1ccccc1S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C24H29Cl2N3O5S/c1-33-22-4-2-3-5-23(22)35(31,32)27-24(30)29-12-8-17(9-13-29)28-14-10-18(11-15-28)34-19-6-7-20(25)21(26)16-19/h2-7,16-18H,8-15H2,1H3,(H,27,30)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(2-methoxyphenyl)sulfonylpiperidine-1-carboxamide\",0.89\nO[C@H]([C@H](Cc1ccccc1)NC(=O)c2cc3cc(Cl)ccc3[nH]2)C(=O)N4C[C@@H](O)[C@@H](O)C4,\"InChI=1S/C23H24ClN3O5/c24-15-6-7-16-14(9-15)10-18(25-16)22(31)26-17(8-13-4-2-1-3-5-13)21(30)23(32)27-11-19(28)20(29)12-27/h1-7,9-10,17,19-21,25,28-30H,8,11-12H2,(H,26,31)/t17-,19-,20+,21+/m0/s1\",[O][C@H1][Branch2][Ring2][C][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2][C][=Branch1][C][=O][N][C][C@@H1][Branch1][C][O][C@@H1][Branch1][C][O][C][Ring1][#Branch1],\"5-chloro-n-[(2s,3r)-4-[(3s,4r)-3,4-dihydroxypyrrolidin-1-yl]-3-hydroxy-4-oxo-1-phenylbutan-2-yl]-1h-indole-2-carboxamide\",2.8\nCC1(C)Cc2c(c3ccccc3)c(c(CC(=O)O)n2C1)c4ccc(Cl)cc4,\"InChI=1S/C23H22ClNO2/c1-23(2)13-19-22(15-6-4-3-5-7-15)21(16-8-10-17(24)11-9-16)18(12-20(26)27)25(19)14-23/h3-11H,12-14H2,1-2H3,(H,26,27)\",[C][C][Branch1][C][C][C][C][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][P][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][Ring1][#C][C][Ring2][Ring1][Ring1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"2-[2-(4-chlorophenyl)-6,6-dimethyl-1-phenyl-5,7-dihydropyrrolizin-3-yl]acetic acid\",3.07\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Oc3cccc4ccccc34)c2C(=O)N5CC[C@@H](O)C5,\"InChI=1S/C26H27N3O5S/c1-15(2)13-29-24-20(22(31)27(3)26(29)33)21(23(32)28-12-11-17(30)14-28)25(35-24)34-19-10-6-8-16-7-4-5-9-18(16)19/h4-10,15,17,30H,11-14H2,1-3H3/t17-/m1/s1\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1],\"5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)-6-naphthalen-1-yloxythieno[3,2-e]pyrimidine-2,4-dione\",2.87\nCCC(=O)NCC[C@@H]1CCc2ccc3OCCc3c12,\"InChI=1S/C16H21NO2/c1-2-15(18)17-9-7-12-4-3-11-5-6-14-13(16(11)12)8-10-19-14/h5-6,12H,2-4,7-10H2,1H3,(H,17,18)/t12-/m0/s1\",[C][C][C][=Branch1][C][=O][N][C][C][C@@H1][C][C][C][=C][C][=C][O][C][C][C][Ring1][Branch1][=C][Ring1][N][Ring1][=Branch2],\"n-[2-[(8s)-2,6,7,8-tetrahydro-1h-cyclopenta[e][1]benzoxol-8-yl]ethyl]propanamide\",2.57\nCN(CCOc1ccc(CC2SC(=O)NC2=O)cc1)c3ccccn3,\"InChI=1S/C18H19N3O3S/c1-21(16-4-2-3-9-19-16)10-11-24-14-7-5-13(6-8-14)12-15-17(22)20-18(23)25-15/h2-9,15H,10-12H2,1H3,(H,20,22,23)\",[C][N][Branch2][Ring1][#Branch2][C][C][O][C][=C][C][=C][Branch1][=N][C][C][S][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=O][C][=C][Ring1][=C][C][=C][C][=C][C][=N][Ring1][=Branch1],\"5-[[4-[2-(methyl-pyridin-2-ylamino)ethoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione\",2.5\nOc1ccc(CC(=O)c2ccc(O)cc2O)cc1,\"InChI=1S/C14H12O4/c15-10-3-1-9(2-4-10)7-13(17)12-6-5-11(16)8-14(12)18/h1-6,8,15-16,18H,7H2\",[O][C][=C][C][=C][Branch2][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][=C][Ring1][P],\"1-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)ethanone\",2.54\nClc1cccc(Cl)c1c2nnc3cccc(Cl)n23,InChI=1S/C12H6Cl3N3/c13-7-3-1-4-8(14)11(7)12-17-16-10-6-2-5-9(15)18(10)12/h1-6H,[Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][N][=C][C][=C][C][=C][Branch1][C][Cl][N][Ring1][#Branch2][Ring1][#Branch1],\"5-chloro-3-(2,6-dichlorophenyl)-[1,2,4]triazolo[4,5-a]pyridine\",2.66\nCNCCCN1c2ccccc2CCc3ccccc13,\"InChI=1S/C18H22N2/c1-19-13-6-14-20-17-9-4-2-7-15(17)11-12-16-8-3-5-10-18(16)20/h2-5,7-10,19H,6,11-14H2,1H3\",[C][N][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n-methylpropan-1-amine\",1.24\nClc1ccc(cc1)S(=O)(=O)Nc2nnc(s2)c3ccccc3,\"InChI=1S/C14H10ClN3O2S2/c15-11-6-8-12(9-7-11)22(19,20)18-14-17-16-13(21-14)10-4-2-1-3-5-10/h1-9H,(H,17,18)\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4-chloro-n-(5-phenyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide\",1.14\nCN1SC(=O)c2cc(ccc12)S(=O)(=O)NC3CC3,\"InChI=1S/C11H12N2O3S2/c1-13-10-5-4-8(6-9(10)11(14)17-13)18(15,16)12-7-2-3-7/h4-7,12H,2-3H2,1H3\",[C][N][S][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][Ring1][Ring1],\"n-cyclopropyl-1-methyl-3-oxo-2,1-benzothiazole-5-sulfonamide\",1.3\nCOc1cc2nc(nc(N)c2cc1OC)N3CCN(CC3)C(=O)C4CCCO4,\"InChI=1S/C19H25N5O4/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14/h10-11,14H,3-9H2,1-2H3,(H2,20,21,22)\",[C][O][C][=C][C][=N][C][=Branch1][#C][=N][C][Branch1][C][N][=C][Ring1][#Branch1][C][=C][Ring1][O][O][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][C][O][Ring1][Branch1],\"[4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl]-(oxolan-2-yl)methanone\",0.9\nCOc1cc(ccc1Cn2ccc3ccc(NC(=O)OC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5,\"InChI=1S/C29H29N3O6S/c1-37-27-17-21(28(33)31-39(35,36)25-9-3-2-4-10-25)11-12-22(27)19-32-16-15-20-13-14-23(18-26(20)32)30-29(34)38-24-7-5-6-8-24/h2-4,9-18,24H,5-8,19H2,1H3,(H,30,34)(H,31,33)\",[C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],cyclopentyl n-[1-[[2-methoxy-4-(phenylsulfonylcarbamoyl)phenyl]methyl]indol-6-yl]carbamate,2.2\nCCCc1c(O)c(ccc1OCc2ccc(cc2)C(=O)O)C(=O)C,\"InChI=1S/C19H20O5/c1-3-4-16-17(10-9-15(12(2)20)18(16)21)24-11-13-5-7-14(8-6-13)19(22)23/h5-10,21H,3-4,11H2,1-2H3,(H,22,23)\",[C][C][C][C][=C][Branch1][C][O][C][=Branch2][Ring1][#Branch1][=C][C][=C][Ring1][#Branch1][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C],4-[(4-acetyl-3-hydroxy-2-propylphenoxy)methyl]benzoic acid,2.1\nClc1ccc(c(Cl)c1)c2nnc3cccc(Cl)n23,InChI=1S/C12H6Cl3N3/c13-7-4-5-8(9(14)6-7)12-17-16-11-3-1-2-10(15)18(11)12/h1-6H,[Cl][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][N][=C][C][=C][C][=C][Branch1][C][Cl][N][Ring1][#Branch2][Ring1][#Branch1],\"5-chloro-3-(2,4-dichlorophenyl)-[1,2,4]triazolo[4,5-a]pyridine\",2.88\nCCn1c(C)ncc1c2ccnc(Nc3ccc(cc3)S(=O)(=O)NCCOC)n2,\"InChI=1S/C19H24N6O3S/c1-4-25-14(2)21-13-18(25)17-9-10-20-19(24-17)23-15-5-7-16(8-6-15)29(26,27)22-11-12-28-3/h5-10,13,22H,4,11-12H2,1-3H3,(H,20,23,24)\",[C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][Branch2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][O][C][=N][Ring2][Ring1][Branch1],4-[[4-(3-ethyl-2-methylimidazol-4-yl)pyrimidin-2-yl]amino]-n-(2-methoxyethyl)benzenesulfonamide,2.44\nCN1CCCCC1CCN2c3ccccc3Sc4ccc(cc24)[S+](C)[O-],\"InChI=1S/C21H26N2OS2/c1-22-13-6-5-7-16(22)12-14-23-18-8-3-4-9-20(18)25-21-11-10-17(26(2)24)15-19(21)23/h3-4,8-11,15-16H,5-7,12-14H2,1-2H3\",[C][N][C][C][C][C][C][Ring1][=Branch1][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][S+1][Branch1][C][C][O-1],10-[2-(1-methylpiperidin-2-yl)ethyl]-2-methylsulfinylphenothiazine,1.6\nNc1ccnc(n1)c2cccnc2,\"InChI=1S/C9H8N4/c10-8-3-5-12-9(13-8)7-2-1-4-11-6-7/h1-6H,(H2,10,12,13)\",[N][C][=C][C][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],2-pyridin-3-ylpyrimidin-4-amine,0.44\nC[C@@H](Oc1cc(cnc1N)c2cnn(c2)C3CCNCC3)c4c(Cl)ccc(F)c4Cl,\"InChI=1S/C21H22Cl2FN5O/c1-12(19-16(22)2-3-17(24)20(19)23)30-18-8-13(9-27-21(18)25)14-10-28-29(11-14)15-4-6-26-7-5-15/h2-3,8-12,15,26H,4-7H2,1H3,(H2,25,27)/t12-/m1/s1\",[C][C@@H1][Branch2][Ring1][=C][O][C][=C][C][=Branch1][#Branch1][=C][N][=C][Ring1][=Branch1][N][C][C][=N][N][Branch1][Ring2][C][=Ring1][Branch1][C][C][C][N][C][C][Ring1][=Branch1][C][=C][Branch1][C][Cl][C][=C][C][Branch1][C][F][=C][Ring1][Branch2][Cl],\"3-[(1r)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-(1-piperidin-4-ylpyrazol-4-yl)pyridin-2-amine\",2.33\nCC1(C)N=C(N)N=C(N)N1c2ccc(Oc3ccc(Cl)cc3)c(Cl)c2,\"InChI=1S/C17H17Cl2N5O/c1-17(2)23-15(20)22-16(21)24(17)11-5-8-14(13(19)9-11)25-12-6-3-10(18)4-7-12/h3-9H,1-2H3,(H4,20,21,22,23)\",[C][C][Branch1][C][C][N][=C][Branch1][C][N][N][=C][Branch1][C][N][N][Ring1][=Branch2][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][=C][Ring1][#C],\"1-[3-chloro-4-(4-chlorophenoxy)phenyl]-6,6-dimethyl-1,3,5-triazine-2,4-diamine\",0.79\nCOc1ccc(cc1)n2cnc3cc(NS(=O)(=O)c4ccccc4)ccc23,\"InChI=1S/C20H17N3O3S/c1-26-17-10-8-16(9-11-17)23-14-21-19-13-15(7-12-20(19)23)22-27(24,25)18-5-3-2-4-6-18/h2-14,22H,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=N][C][=C][C][Branch1][P][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Ring1][Ring1][S],n-[1-(4-methoxyphenyl)benzimidazol-5-yl]benzenesulfonamide,3.7\nOC(=O)c1cc2cc(OCc3ccccc3)ccc2[nH]1,\"InChI=1S/C16H13NO3/c18-16(19)15-9-12-8-13(6-7-14(12)17-15)20-10-11-4-2-1-3-5-11/h1-9,17H,10H2,(H,18,19)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring1][=C][NH1][Ring1][P],5-(phenylmethoxy)-1h-indole-2-carboxylic acid,0.4\nNc1cc(c(cn1)c2cc(nc(n2)N3CCOCC3)N4CCOCC4)C(F)(F)F,\"InChI=1S/C18H21F3N6O2/c19-18(20,21)13-9-15(22)23-11-12(13)14-10-16(26-1-5-28-6-2-26)25-17(24-14)27-3-7-29-8-4-27/h9-11H,1-8H2,(H2,22,23)\",[N][C][=C][C][=Branch2][Ring2][Ring2][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"5-[2,6-di(morpholin-4-yl)pyrimidin-4-yl]-4-(trifluoromethyl)pyridin-2-amine\",2.7\nCNC(=O)c1cc(sc1NC(=O)N)c2ccccc2,\"InChI=1S/C13H13N3O2S/c1-15-11(17)9-7-10(8-5-3-2-4-6-8)19-12(9)16-13(14)18/h2-7H,1H3,(H,15,17)(H3,14,16,18)\",[C][N][C][=Branch1][C][=O][C][C][=C][Branch1][O][S][C][=Ring1][Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(carbamoylamino)-n-methyl-5-phenylthiophene-3-carboxamide,3.19\nC[C@H](NC(=O)Cc1cc(F)cc(F)c1)C(=O)NC2C(=O)N(C)c3ccccc3c4ccccc24,\"InChI=1S/C26H23F2N3O3/c1-15(29-23(32)13-16-11-17(27)14-18(28)12-16)25(33)30-24-21-9-4-3-7-19(21)20-8-5-6-10-22(20)31(2)26(24)34/h3-12,14-15,24H,13H2,1-2H3,(H,29,32)(H,30,33)/t15-,24?/m0/s1\",[C][C@H1][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][C][=Branch1][C][=O][N][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1],\"(2s)-2-[[2-(3,5-difluorophenyl)acetyl]amino]-n-(5-methyl-6-oxo-7h-benzo[d][1]benzazepin-7-yl)propanamide\",3.6\nC[C@H](NC(=O)c1cccc2CCN(Cc3ccc(Cl)cc3)c12)c4ccc(cc4)C(=O)O,\"InChI=1S/C25H23ClN2O3/c1-16(18-7-9-20(10-8-18)25(30)31)27-24(29)22-4-2-3-19-13-14-28(23(19)22)15-17-5-11-21(26)12-6-17/h2-12,16H,13-15H2,1H3,(H,27,29)(H,30,31)/t16-/m0/s1\",[C][C@H1][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][=C][C][C][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Ring1][P][=Ring1][=N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O],\"4-[(1s)-1-[[1-[(4-chlorophenyl)methyl]2,3-dihydroindole-7-carbonyl]amino]ethyl]benzoic acid\",1.47\nCC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccc(F)cc2)C(F)(F)F,\"InChI=1S/C16H13F4NO4S/c1-15(23,16(18,19)20)14(22)21-11-4-8-13(9-5-11)26(24,25)12-6-2-10(17)3-7-12/h2-9,23H,1H3,(H,21,22)\",[C][C][Branch1][C][O][Branch2][Ring2][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F],\"3,3,3-trifluoro-n-[4-(4-fluorophenyl)sulfonylphenyl]-2-hydroxy-2-methylpropanamide\",3.12\nC[C@@H]1CN(C[C@H](C)N1)c2c(F)c(N)c3C(=O)C(=CN(C4CC4)c3c2F)C(=O)O,\"InChI=1S/C19H22F2N4O3/c1-8-5-24(6-9(2)23-8)17-13(20)15(22)12-16(14(17)21)25(10-3-4-10)7-11(18(12)26)19(27)28/h7-10,23H,3-6,22H2,1-2H3,(H,27,28)/t8-,9+\",[C][C@@H1][C][N][Branch1][=Branch2][C][C@H1][Branch1][C][C][N][Ring1][#Branch1][C][=C][Branch1][C][F][C][Branch1][C][N][=C][C][=Branch1][C][=O][C][=Branch1][P][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring1][#Branch2][=C][Ring1][S][F][C][=Branch1][C][=O][O],\"5-amino-1-cyclopropyl-7-[(3s,5r)-3,5-dimethylpiperazin-1-yl]-6,8-difluoro-4-oxoquinoline-3-carboxylic acid\",-0.15\nClc1cccc(NNC(=O)c2cccnc2Cl)c1,\"InChI=1S/C12H9Cl2N3O/c13-8-3-1-4-9(7-8)16-17-12(18)10-5-2-6-15-11(10)14/h1-7,16H,(H,17,18)\",[Cl][C][=C][C][=C][C][Branch1][S][N][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][Cl][=C][Ring1][P],2-chloro-n'-(3-chlorophenyl)pyridine-3-carbohydrazide,1.87\nCc1ccc(NC(=O)CCC2CCCCC2)cc1NC(=O)c3ccc(O)cc3,\"InChI=1S/C23H28N2O3/c1-16-7-11-19(24-22(27)14-8-17-5-3-2-4-6-17)15-21(16)25-23(28)18-9-12-20(26)13-10-18/h7,9-13,15,17,26H,2-6,8,14H2,1H3,(H,24,27)(H,25,28)\",[C][C][=C][C][=C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],n-[5-(3-cyclohexylpropanoylamino)-2-methylphenyl]-4-hydroxybenzamide,4.13\nCCc1c(C(=O)C(=O)N)c2c(OCC(=O)N)cccc2n1Cc3ccccc3,\"InChI=1S/C21H21N3O4/c1-2-14-19(20(26)21(23)27)18-15(9-6-10-16(18)28-12-17(22)25)24(14)11-13-7-4-3-5-8-13/h3-10H,2,11-12H2,1H3,(H2,22,25)(H2,23,27)\",[C][C][C][=C][Branch1][#Branch2][C][=Branch1][C][=O][C][=Branch1][C][=O][N][C][=C][Branch1][Branch2][O][C][C][=Branch1][C][=O][N][C][=C][C][=C][Ring1][O][N][Ring2][Ring1][Ring1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-(2-amino-2-oxoethoxy)-2-ethyl-1-(phenylmethyl)indol-3-yl]-2-oxoacetamide,2.1\nNc1cccc2C(=O)C(=O)c3ccccc3c12,\"InChI=1S/C14H9NO2/c15-11-7-3-6-10-12(11)8-4-1-2-5-9(8)13(16)14(10)17/h1-7H,15H2\",[N][C][=C][C][=C][C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][S][=Ring1][N],\"4-aminophenanthrene-9,10-dione\",2.31\nCOc1ccc2cc(ccc2c1)C(C)C(=O)O,\"InChI=1S/C14H14O3/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10/h3-9H,1-2H3,(H,15,16)\",[C][O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][Branch1][C][C][C][=Branch1][C][=O][O],2-(6-methoxynaphthalen-2-yl)propanoic acid,0.23\nC1NC(Cc2ccccc12)c3ccccc3,\"InChI=1S/C15H15N/c1-2-6-12(7-3-1)15-10-13-8-4-5-9-14(13)11-16-15/h1-9,15-16H,10-11H2\",[C][N][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-phenyl-1,2,3,4-tetrahydroisoquinoline\",1.9\nCCN(CC)S(=O)(=O)c1ccc(cc1)c2cc(ccc2OCC(=O)O)C(F)(F)F,\"InChI=1S/C19H20F3NO5S/c1-3-23(4-2)29(26,27)15-8-5-13(6-9-15)16-11-14(19(20,21)22)7-10-17(16)28-12-18(24)25/h5-11H,3-4,12H2,1-2H3,(H,24,25)\",[C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=N][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F],2-[2-[4-(diethylsulfamoyl)phenyl]-4-(trifluoromethyl)phenoxy]acetic acid,0.67\nCN(C)CCOC(C)(c1ccccc1)c2ccccn2,\"InChI=1S/C17H22N2O/c1-17(20-14-13-19(2)3,15-9-5-4-6-10-15)16-11-7-8-12-18-16/h4-12H,13-14H2,1-3H3\",[C][N][Branch1][C][C][C][C][O][C][Branch1][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1],\"n,n-dimethyl-2-(1-phenyl-1-pyridin-2-ylethoxy)ethanamine\",-0.2\nCOc1ccc(C(=O)Nc2c(Cl)cncc2Cl)c3cccnc13,\"InChI=1S/C16H11Cl2N3O2/c1-23-13-5-4-10(9-3-2-6-20-14(9)13)16(22)21-15-11(17)7-19-8-12(15)18/h2-8H,1H3,(H,19,21,22)\",[C][O][C][=C][C][=C][Branch2][Ring1][C][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=N][C][=C][Ring1][#Branch1][Cl][C][=C][C][=C][N][=C][Ring2][Ring1][Branch1][Ring1][=Branch1],\"n-(3,5-dichloropyridin-4-yl)-8-methoxyquinoline-5-carboxamide\",2.09\nCOc1ccc(Cl)cc1C(=O)NCCc2ccc(cc2)S(=O)(=O)NC(=O)NC3CCCCC3,\"InChI=1S/C23H28ClN3O5S/c1-32-21-12-9-17(24)15-20(21)22(28)25-14-13-16-7-10-19(11-8-16)33(30,31)27-23(29)26-18-5-3-2-4-6-18/h7-12,15,18H,2-6,13-14H2,1H3,(H,25,28)(H2,26,27,29)\",[C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1],5-chloro-n-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-2-methoxybenzamide,2.23\nOCC(=O)N1CCC[C@@H]1COc2cccc3ncnc(Nc4ccc(OCc5ccccn5)c(Cl)c4)c23,\"InChI=1S/C27H26ClN5O4/c28-21-13-18(9-10-23(21)36-15-19-5-1-2-11-29-19)32-27-26-22(30-17-31-27)7-3-8-24(26)37-16-20-6-4-12-33(20)25(35)14-34/h1-3,5,7-11,13,17,20,34H,4,6,12,14-16H2,(H,30,31,32)/t20-/m1/s1\",[O][C][C][=Branch1][C][=O][N][C][C][C][C@@H1][Ring1][Branch1][C][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring1][#C][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1],1-[(2r)-2-[[4-[[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]amino]quinazolin-5-yl]oxymethyl]pyrrolidin-1-yl]-2-hydroxyethanone,3.71\nCCN(CC)C(C)C(=O)c1ccccc1,\"InChI=1S/C13H19NO/c1-4-14(5-2)11(3)13(15)12-9-7-6-8-10-12/h6-11H,4-5H2,1-3H3\",[C][C][N][Branch1][Ring1][C][C][C][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-diethylamino-1-phenylpropan-1-one,1.18\nCCCN(CCC)C(=O)c1cccc(c1)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc3cccc(OC)c3,\"InChI=1S/C32H41N3O4/c1-4-17-35(18-5-2)32(38)27-15-10-14-26(21-27)31(37)34-29(20-24-11-7-6-8-12-24)30(36)23-33-22-25-13-9-16-28(19-25)39-3/h6-16,19,21,29-30,33,36H,4-5,17-18,20,22-23H2,1-3H3,(H,34,37)/t29-,30+/m0/s1\",[C][C][C][N][Branch1][Ring2][C][C][C][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C@H1][Branch1][C][O][C][N][C][C][=C][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2],\"n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]-n',n'-dipropylbenzene-1,3-dicarboxamide\",2.7\nOC(=O)c1ccc(cc1)c2nnn(Cc3ccccc3F)n2,\"InChI=1S/C15H11FN4O2/c16-13-4-2-1-3-12(13)9-20-18-14(17-19-20)10-5-7-11(8-6-10)15(21)22/h1-8H,9H2,(H,21,22)\",[O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=N][N][Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][N][=Ring1][=N],4-[2-[(2-fluorophenyl)methyl]tetrazol-5-yl]benzoic acid,0.3\nCC(C)NCC(O)COc1nccs1,\"InChI=1S/C9H16N2O2S/c1-7(2)11-5-8(12)6-13-9-10-3-4-14-9/h3-4,7-8,11-12H,5-6H2,1-2H3\",[C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=N][C][=C][S][Ring1][Branch1],\"1-(propan-2-ylamino)-3-(1,3-thiazol-2-yloxy)propan-2-ol\",-0.97\nCC(C)NCC(O)COc1ccccc1CC=C,\"InChI=1S/C15H23NO2/c1-4-7-13-8-5-6-9-15(13)18-11-14(17)10-16-12(2)3/h4-6,8-9,12,14,16-17H,1,7,10-11H2,2-3H3\",[C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C],1-(propan-2-ylamino)-3-(2-prop-2-enylphenoxy)propan-2-ol,0.99\nOC(=O)c1ccccc1O,\"InChI=1S/C7H6O3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H,(H,9,10)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O],2-hydroxybenzoic acid,-1.36\nCn1cnc(c2ccccc2)c1c3cc4c(N)ncnc4s3,\"InChI=1S/C16H13N5S/c1-21-9-20-13(10-5-3-2-4-6-10)14(21)12-7-11-15(17)18-8-19-16(11)22-12/h2-9H,1H3,(H2,17,18,19)\",[C][N][C][=N][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Ring1][O][C][=C][C][C][Branch1][C][N][=N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2],\"6-(3-methyl-5-phenylimidazol-4-yl)thieno[3,2-e]pyrimidin-4-amine\",2.94\nCCCCNC(=O)NS(=O)(=O)c1ccc(C)cc1,\"InChI=1S/C12H18N2O3S/c1-3-4-9-13-12(15)14-18(16,17)11-7-5-10(2)6-8-11/h5-8H,3-4,9H2,1-2H3,(H2,13,14,15)\",[C][C][C][C][N][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],1-butyl-3-(4-methylphenyl)sulfonylurea,0.44\nCOc1ccc(Cl)c(Nc2ncnc3cc(OC)cc(OC4CCN(C)CC4)c23)c1,\"InChI=1S/C22H25ClN4O3/c1-27-8-6-14(7-9-27)30-20-12-16(29-3)11-19-21(20)22(25-13-24-19)26-18-10-15(28-2)4-5-17(18)23/h4-5,10-14H,6-9H2,1-3H3,(H,24,25,26)\",[C][O][C][=C][C][=C][Branch1][C][Cl][C][Branch2][Ring2][Ring1][N][C][=N][C][=N][C][=C][C][Branch1][Ring1][O][C][=C][C][Branch1][=N][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][Ring2][Ring1][Ring2][Ring1][S][=C][Ring2][Ring1][N],n-(2-chloro-5-methoxyphenyl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine,3.6\nCc1ccc2nc(CCNCCCO)ccc2c1NC(=O)CC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C27H37N3O2/c1-18-3-6-24-23(5-4-22(29-24)7-9-28-8-2-10-31)26(18)30-25(32)17-27-14-19-11-20(15-27)13-21(12-19)16-27/h3-6,19-21,28,31H,2,7-17H2,1H3,(H,30,32)\",[C][C][=C][C][=C][N][=C][Branch1][Branch2][C][C][N][C][C][C][O][C][=C][C][Ring1][=N][=C][Ring1][P][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],2-(1-adamantyl)-n-[2-[2-(3-hydroxypropylamino)ethyl]-6-methylquinolin-5-yl]acetamide,1.18\nCN(C)CC(O)COc1ccc(Nc2ncc(C)c(Nc3ccccc3)n2)cc1,\"InChI=1S/C22H27N5O2/c1-16-13-23-22(26-21(16)24-17-7-5-4-6-8-17)25-18-9-11-20(12-10-18)29-15-19(28)14-27(2)3/h4-13,19,28H,14-15H2,1-3H3,(H2,23,24,25,26)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][Branch1][C][C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1],1-dimethylamino-3-[4-[[5-methyl-4-(phenylamino)pyrimidin-2-yl]amino]phenoxy]propan-2-ol,2\nCOc1cc2ncc(C(=O)N)c(Nc3cccc(Cl)c3)c2cc1OC,\"InChI=1S/C18H16ClN3O3/c1-24-15-7-12-14(8-16(15)25-2)21-9-13(18(20)23)17(12)22-11-5-3-4-10(19)6-11/h3-9H,1-2H3,(H2,20,23)(H,21,22)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C],\"4-[(3-chlorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",3.5\nC[C@@H]1CN[C@@H]2[C@@H](C1)O[C@]3(CC[C@H]4[C@@H]5CC=C6C[C@@H](O)CC[C@]6(C)[C@H]5CC4=C3C)[C@@H]2C,\"InChI=1S/C27H41NO2/c1-15-11-24-25(28-14-15)17(3)27(30-24)10-8-20-21-6-5-18-12-19(29)7-9-26(18,4)23(21)13-22(20)16(27)2/h5,15,17,19-21,23-25,28-29H,6-14H2,1-4H3/t15-,17+,19-,20-,21-,23-,24+,25-,26-,27-/m0/s1\",[C][C@@H1][C][N][C@@H1][C@@H1][Branch1][Ring2][C][Ring1][=Branch1][O][C@][Branch2][Ring1][P][C][C][C@H1][C@@H1][C][C][=C][C][C@@H1][Branch1][C][O][C][C][C@][Ring1][#Branch1][Branch1][C][C][C@H1][Ring1][N][C][C][Ring1][#C][=C][Ring2][Ring1][Ring1][C][C@@H1][Ring2][Ring1][=Branch2][C],\"(3s,3'r,3'as,6's,6as,6bs,7'ar,9r,11as,11br)-3',6',10,11b-tetramethylspiro[2,3,4,6,6a,6b,7,8,11,11a-decahydro-1h-benzo[i]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3h-furo[4,5-b]pyridine]-3-ol\",2.63\nNC(=O)N1c2ccccc2C[C@H](O)c3ccccc13,\"InChI=1S/C15H14N2O2/c16-15(19)17-12-7-3-1-5-10(12)9-14(18)11-6-2-4-8-13(11)17/h1-8,14,18H,9H2,(H2,16,19)/t14-/m0/s1\",[N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C@H1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1],\"(6s)-6-hydroxy-5,6-dihydrobenzo[b][1]benzazepine-11-carboxamide\",0.79\nNc1nnc(s1)c2ccccc2,\"InChI=1S/C8H7N3S/c9-8-11-10-7(12-8)6-4-2-1-3-5-6/h1-5H,(H2,9,11)\",[N][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-phenyl-1,3,4-thiadiazol-2-amine\",1.8\nCOc1ncnc(NS(=O)(=O)c2ccc(N)cc2)c1OC,\"InChI=1S/C12H14N4O4S/c1-19-10-11(14-7-15-12(10)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16)\",[C][O][C][=N][C][=N][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][=C][Ring1][P][O][C],\"4-amino-n-(5,6-dimethoxypyrimidin-4-yl)benzenesulfonamide\",-0.73\nCC(N1NC(=O)C2=C(C1=O)C(=O)c3ccc(Cl)cc3N2)c4ccsc4,\"InChI=1S/C17H12ClN3O3S/c1-8(9-4-5-25-7-9)21-17(24)13-14(16(23)20-21)19-12-6-10(18)2-3-11(12)15(13)22/h2-8H,1H3,(H,19,22)(H,20,23)\",[C][C][Branch2][Ring1][P][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][C][=C][S][C][=Ring1][Branch1],\"7-chloro-2-(1-thiophen-3-ylethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",0.9\nCCN1CCN(CC1)C(=O)c2cc3cc(F)ccc3[nH]2,\"InChI=1S/C15H18FN3O/c1-2-18-5-7-19(8-6-18)15(20)14-10-11-9-12(16)3-4-13(11)17-14/h3-4,9-10,17H,2,5-8H2,1H3\",[C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],(4-ethylpiperazin-1-yl)-(5-fluoro-1h-indol-2-yl)methanone,2.28\nCN1CCC[C@@H]1CCO[C@](C)(c2ccccc2)c3ccc(Cl)cc3,\"InChI=1S/C21H26ClNO/c1-21(17-7-4-3-5-8-17,18-10-12-19(22)13-11-18)24-16-14-20-9-6-15-23(20)2/h3-5,7-8,10-13,20H,6,9,14-16H2,1-2H3/t20-,21-/m1/s1\",[C][N][C][C][C][C@@H1][Ring1][Branch1][C][C][O][C@][Branch1][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],(2r)-2-[2-[(1r)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine,3.48\nO=C(N[C@H]1CN2CCC1CC2)c3ccc(s3)c4ccccc4,\"InChI=1S/C18H20N2OS/c21-18(19-15-12-20-10-8-13(15)9-11-20)17-7-6-16(22-17)14-4-2-1-3-5-14/h1-7,13,15H,8-12H2,(H,19,21)/t15-/m0/s1\",[O][=C][Branch1][=C][N][C@H1][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-[(8r)-1-azabicyclo[2.2.2]octan-8-yl]-5-phenylthiophene-2-carboxamide,1.9\nCC(NCC(O)c1ccc(cc1)[N+](=O)[O-])C23CC4CC(CC(C4)C2)C3,\"InChI=1S/C20H28N2O3/c1-13(20-9-14-6-15(10-20)8-16(7-14)11-20)21-12-19(23)17-2-4-18(5-3-17)22(24)25/h2-5,13-16,19,21,23H,6-12H2,1H3\",[C][C][Branch2][Ring1][=Branch1][N][C][C][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],2-[1-(1-adamantyl)ethylamino]-1-(4-nitrophenyl)ethanol,3.53\nOC(=O)c1ccc2c(c1)nc(Nc3cccc(Cl)c3)c4ccncc24,\"InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=N][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1],\"5-[(3-chlorophenyl)amino]pyrido[4,3-c]quinoline-8-carboxylic acid\",1.29\nCN1CCCC(COc2nccc(Nc3cc(NC(=O)c4ccnc(c4)N5CCOCC5)ccc3C)n2)C1,\"InChI=1S/C28H35N7O3/c1-20-5-6-23(31-27(36)22-7-9-29-26(16-22)35-12-14-37-15-13-35)17-24(20)32-25-8-10-30-28(33-25)38-19-21-4-3-11-34(2)18-21/h5-10,16-17,21H,3-4,11-15,18-19H2,1-2H3,(H,31,36)(H,30,32,33)\",[C][N][C][C][C][C][Branch2][Branch1][Ring2][C][O][C][=N][C][=C][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=N][Ring2][Ring1][=N][C][Ring2][Ring2][Branch1],n-[4-methyl-3-[[2-[(1-methylpiperidin-3-yl)methoxy]pyrimidin-4-yl]amino]phenyl]-2-morpholin-4-ylpyridine-4-carboxamide,1.9\nCN(C)CCCN(C)S(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1,\"InChI=1S/C23H27N7O2S/c1-28(2)14-6-15-29(3)33(31,32)19-10-8-18(9-11-19)26-23-24-13-12-20(27-23)21-17-25-22-7-4-5-16-30(21)22/h4-5,7-13,16-17H,6,14-15H2,1-3H3,(H,24,26,27)\",[C][N][Branch1][C][C][C][C][C][N][Branch1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"n-(3-dimethylaminopropyl)-4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]-n-methylbenzenesulfonamide\",2.16\nOC1=CC(=O)C2=C(O1)c3ccccc3N(Cc4ccccc4)C2=O,\"InChI=1S/C19H13NO4/c21-15-10-16(22)24-18-13-8-4-5-9-14(13)20(19(23)17(15)18)11-12-6-2-1-3-7-12/h1-10,22H,11H2\",[O][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Ring2][O][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][C][=O],\"2-hydroxy-6-(phenylmethyl)pyrano[3,2-c]quinoline-4,5-dione\",1.97\nCC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccc(O)cc2)C(F)(F)F,\"InChI=1S/C16H14F3NO5S/c1-15(23,16(17,18)19)14(22)20-10-2-6-12(7-3-10)26(24,25)13-8-4-11(21)5-9-13/h2-9,21,23H,1H3,(H,20,22)\",[C][C][Branch1][C][O][Branch2][Ring2][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F],\"3,3,3-trifluoro-2-hydroxy-n-[4-(4-hydroxyphenyl)sulfonylphenyl]-2-methylpropanamide\",2.78\nFc1cccc(F)c1CS(=O)(=O)N2CCN(CC2)c3ncccc3C(F)(F)F,\"InChI=1S/C17H16F5N3O2S/c18-14-4-1-5-15(19)12(14)11-28(26,27)25-9-7-24(8-10-25)16-13(17(20,21)22)3-2-6-23-16/h1-6H,7-11H2\",[F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"1-[(2,6-difluorophenyl)methylsulfonyl]-4-[3-(trifluoromethyl)pyridin-2-yl]piperazine\",3.9\nCc1onc(C(=O)N)c1C(=O)Nc2nccs2,\"InChI=1S/C9H8N4O3S/c1-4-5(6(7(10)14)13-16-4)8(15)12-9-11-2-3-17-9/h2-3H,1H3,(H2,10,14)(H,11,12,15)\",[C][C][O][N][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=Ring1][Branch2][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"5-methyl-n'-(1,3-thiazol-2-yl)-1,2-oxazole-3,4-dicarboxamide\",1.63\nCNCCC(Oc1ccc(cc1)C(F)(F)F)c2ccccc2,\"InChI=1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3\",[C][N][C][C][C][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1],n-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine,1.92\nCCn1cnc(c2ccccc2)c1c3nc4c(N)ncnc4s3,\"InChI=1S/C16H14N6S/c1-2-22-9-20-11(10-6-4-3-5-7-10)13(22)16-21-12-14(17)18-8-19-15(12)23-16/h3-9H,2H2,1H3,(H2,17,18,19)\",[C][C][N][C][=N][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Ring1][O][C][=N][C][C][Branch1][C][N][=N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2],\"2-(3-ethyl-5-phenylimidazol-4-yl)-[1,3]thiazolo[4,5-e]pyrimidin-7-amine\",2.97\nCN(c1ncccc1CNc2nc(Nc3ccc4NC(=O)Cc4c3)ncc2C(F)(F)F)S(=O)(=O)C,\"InChI=1S/C21H20F3N7O3S/c1-31(35(2,33)34)19-12(4-3-7-25-19)10-26-18-15(21(22,23)24)11-27-20(30-18)28-14-5-6-16-13(8-14)9-17(32)29-16/h3-8,11H,9-10H2,1-2H3,(H,29,32)(H2,26,27,28,30)\",[C][N][Branch2][Ring2][#C][C][=N][C][=C][C][=C][Ring1][=Branch1][C][N][C][=N][C][Branch2][Ring1][C][N][C][=C][C][=C][N][C][=Branch1][C][=O][C][C][Ring1][=Branch1][=C][Ring1][#Branch2][=N][C][=C][Ring1][P][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C],\"n-methyl-n-[3-[[[2-[(2-oxo-1,3-dihydroindol-5-yl)amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]methyl]pyridin-2-yl]methanesulfonamide\",2.63\nCOCCOc1nc(N)c2NC(=O)N(Cc3cccc(CC(=O)OC)c3)c2n1,\"InChI=1S/C18H21N5O5/c1-26-6-7-28-17-21-15(19)14-16(22-17)23(18(25)20-14)10-12-5-3-4-11(8-12)9-13(24)27-2/h3-5,8H,6-7,9-10H2,1-2H3,(H,20,25)(H2,19,21,22)\",[C][O][C][C][O][C][=N][C][Branch1][C][N][=C][N][C][=Branch1][C][=O][N][Branch2][Ring1][Ring1][C][C][=C][C][=C][C][Branch1][Branch2][C][C][=Branch1][C][=O][O][C][=C][Ring1][O][C][Ring2][Ring1][C][=N][Ring2][Ring1][#Branch1],methyl 2-[3-[[6-amino-2-(2-methoxyethoxy)-8-oxo-7h-purin-9-yl]methyl]phenyl]acetate,1.86\nC[S+]([O-])c1ccc(cc1)c2nc(c3ccc(F)cc3)c([nH]2)c4ccncc4,\"InChI=1S/C21H16FN3OS/c1-27(26)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)\",[C][S+1][Branch1][C][O-1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][Branch1][N][C][C][=C][C][Branch1][C][F][=C][C][=Ring1][#Branch1][=C][Branch1][Ring2][NH1][Ring1][N][C][C][=C][N][=C][C][=Ring1][=Branch1],4-[5-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-3h-imidazol-4-yl]pyridine,3.34\nCC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3Cc4cccnc4C3)c(F)c2,\"InChI=1S/C19H19FN4O3/c1-12(25)22-8-15-10-24(19(26)27-15)14-4-5-18(16(20)7-14)23-9-13-3-2-6-21-17(13)11-23/h2-7,15H,8-11H2,1H3,(H,22,25)/t15-/m0/s1\",[C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][=C][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][Ring1][=Branch2][C][Branch1][C][F][=C][Ring1][S],\"n-[[(5s)-3-[4-(5,7-dihydropyrrolo[3,4-b]pyridin-6-yl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\",2.88\nOCC(=O)N1CCC(CC1)c2[nH]nc(c3ccc(Cl)cc3F)c2c4ccncn4,\"InChI=1S/C20H19ClFN5O2/c21-13-1-2-14(15(22)9-13)20-18(16-3-6-23-11-24-16)19(25-26-20)12-4-7-27(8-5-12)17(29)10-28/h1-3,6,9,11-12,28H,4-5,7-8,10H2,(H,25,26)\",[O][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][NH1][N][=C][Branch1][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][C][=Ring1][=N][C][=C][C][=N][C][=N][Ring1][=Branch1],1-[4-[5-(4-chloro-2-fluorophenyl)-4-pyrimidin-4-yl-2h-pyrazol-3-yl]piperidin-1-yl]-2-hydroxyethanone,1.79\nCC(C)n1c(C)ncc1c2ccnc(Nc3ccc(C(=O)NCCN(C)C)c(F)c3)n2,\"InChI=1S/C22H28FN7O/c1-14(2)30-15(3)26-13-20(30)19-8-9-25-22(28-19)27-16-6-7-17(18(23)12-16)21(31)24-10-11-29(4)5/h6-9,12-14H,10-11H2,1-5H3,(H,24,31)(H,25,27,28)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][=N][C][=Branch1][C][=O][N][C][C][N][Branch1][C][C][C][C][Branch1][C][F][=C][Ring1][#C][=N][Ring2][Ring1][=Branch1],n-(2-dimethylaminoethyl)-2-fluoro-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide,1.96\nCC1(CCC(=O)N1Cc2cccs2)C(=O)NC3CCCCC3,\"InChI=1S/C17H24N2O2S/c1-17(16(21)18-13-6-3-2-4-7-13)10-9-15(20)19(17)12-14-8-5-11-22-14/h5,8,11,13H,2-4,6-7,9-10,12H2,1H3,(H,18,21)\",[C][C][Branch2][Ring1][C][C][C][C][=Branch1][C][=O][N][Ring1][=Branch1][C][C][=C][C][=C][S][Ring1][Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1],n-cyclohexyl-2-methyl-5-oxo-1-(thiophen-2-ylmethyl)pyrrolidine-2-carboxamide,2.15\nNc1nc(SCc2ccccc2)nc3c1ncn3[C@@H]4O[C@H](CO)[C@@H](O)[C@H]4O,\"InChI=1S/C17H19N5O4S/c18-14-11-15(21-17(20-14)27-7-9-4-2-1-3-5-9)22(8-19-11)16-13(25)12(24)10(6-23)26-16/h1-5,8,10,12-13,16,23-25H,6-7H2,(H2,18,20,21)/t10-,12-,13-,16-/m1/s1\",[N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][=C][Ring1][=C][N][=C][N][Ring1][Branch1][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O],\"(2r,3r,4s,5r)-2-[6-amino-2-(phenylmethylsulfanyl)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol\",1.24\nCOc1ccc2cc(ccc2c1)[C@H](C)C(=O)O,\"InChI=1S/C14H14O3/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10/h3-9H,1-2H3,(H,15,16)/t9-/m0/s1\",[C][O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C@H1][Branch1][C][C][C][=Branch1][C][=O][O],(2s)-2-(6-methoxynaphthalen-2-yl)propanoic acid,0.13\nCN(C)C1=C(C)N(C)N(C1=O)c2ccccc2,\"InChI=1S/C13H17N3O/c1-10-12(14(2)3)13(17)16(15(10)4)11-8-6-5-7-9-11/h5-9H,1-4H3\",[C][N][Branch1][C][C][C][=C][Branch1][C][C][N][Branch1][C][C][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4-dimethylamino-1,5-dimethyl-2-phenylpyrazol-3-one\",0.78\nCCC(CC)CNC(=O)c1ccc2c(c1)c(Cc3ccc(cc3OC)C(=O)NS(=O)(=O)c4ccccc4C)cn2C,\"InChI=1S/C32H37N3O5S/c1-6-22(7-2)19-33-31(36)24-14-15-28-27(17-24)26(20-35(28)4)16-23-12-13-25(18-29(23)40-5)32(37)34-41(38,39)30-11-9-8-10-21(30)3/h8-15,17-18,20,22H,6-7,16,19H2,1-5H3,(H,33,36)(H,34,37)\",[C][C][C][Branch1][Ring1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch2][Ring2][Ring1][C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][N][Ring2][Ring1][N][C],n-(2-ethylbutyl)-3-[[2-methoxy-4-[(2-methylphenyl)sulfonylcarbamoyl]phenyl]methyl]-1-methylindole-5-carboxamide,2.7\nCC(C(=O)O)c1ccc(c(F)c1)c2ccccc2,\"InChI=1S/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)\",[C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][F][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(3-fluoro-4-phenylphenyl)propanoic acid,0.85\nCOC[C@H](C)Oc1cc(Oc2cc(F)cc(F)c2)cc(c1)C(=O)Nc3ccc(cn3)C(=O)O,\"InChI=1S/C23H20F2N2O6/c1-13(12-31-2)32-18-5-15(22(28)27-21-4-3-14(11-26-21)23(29)30)6-19(10-18)33-20-8-16(24)7-17(25)9-20/h3-11,13H,12H2,1-2H3,(H,29,30)(H,26,27,28)/t13-/m0/s1\",[C][O][C][C@H1][Branch1][C][C][O][C][=C][C][Branch1][S][O][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][=C][C][=Branch1][Ring2][=C][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O],\"6-[[3-(3,5-difluorophenoxy)-5-[(2s)-1-methoxypropan-2-yl]oxybenzoyl]amino]pyridine-3-carboxylic acid\",1.36\nCSCc1cc(nc(n1)c2ccccc2)N3CCOCC3,\"InChI=1S/C16H19N3OS/c1-21-12-14-11-15(19-7-9-20-10-8-19)18-16(17-14)13-5-3-2-4-6-13/h2-6,11H,7-10,12H2,1H3\",[C][S][C][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],4-(methylsulfanylmethyl)-6-morpholin-4-yl-2-phenylpyrimidine,3.26\nOc1ccc(cc1)C2=COc3cc(O)ccc3C2=O,\"InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)13-8-19-14-7-11(17)5-6-12(14)15(13)18/h1-8,16-17H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][C][Ring1][O][=O],7-hydroxy-3-(4-hydroxyphenyl)chromen-4-one,2.46\nCN1C(=O)C(=Cc2cnc(NC(CCO)CCO)nc12)Oc3ccc(F)cc3F,\"InChI=1S/C19H20F2N4O4/c1-25-17-11(10-22-19(24-17)23-13(4-6-26)5-7-27)8-16(18(25)28)29-15-3-2-12(20)9-14(15)21/h2-3,8-10,13,26-27H,4-7H2,1H3,(H,22,23,24)\",[C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][=Branch2][=C][C][=C][N][=C][Branch1][O][N][C][Branch1][Ring2][C][C][O][C][C][O][N][=C][Ring2][Ring1][Ring1][Ring1][=C][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F],\"6-(2,4-difluorophenoxy)-2-(1,5-dihydroxypentan-3-ylamino)-8-methylpyrido[6,5-d]pyrimidin-7-one\",1.5\nCCc1ccc(NC(=O)c2ccc3cc(ccc3c2)C(=N)N)cc1,\"InChI=1S/C20H19N3O/c1-2-13-3-9-18(10-4-13)23-20(24)17-8-6-14-11-16(19(21)22)7-5-15(14)12-17/h3-12H,2H2,1H3,(H3,21,22)(H,23,24)\",[C][C][C][=C][C][=C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=Branch1][C][=N][N][C][=C][Ring2][Ring1][=Branch1],6-carbamimidoyl-n-(4-ethylphenyl)naphthalene-2-carboxamide,1.1\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC=O)C(=O)C(F)(F)F,\"InChI=1S/C20H20F3N3O4/c1-12(2)17(18(29)20(21,22)23)25-16(28)10-26-15(13-6-4-3-5-7-13)9-8-14(19(26)30)24-11-27/h3-9,11-12,17H,10H2,1-2H3,(H,24,27)(H,25,28)\",[C][C][Branch1][C][C][C][Branch2][Ring1][#C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-(3-formamido-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.84\nNc1cccc2C(=O)N(Cc3cccc(Cl)c3)C(=O)c12,\"InChI=1S/C15H11ClN2O2/c16-10-4-1-3-9(7-10)8-18-14(19)11-5-2-6-12(17)13(11)15(18)20/h1-7H,8,17H2\",[N][C][=C][C][=C][C][C][=Branch1][C][=O][N][Branch1][=N][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Ring2][Ring1][Ring1][=Ring1][#C],\"4-amino-2-[(3-chlorophenyl)methyl]isoindole-1,3-dione\",3.18\nNC(=O)Nc1cc(sc1C(=O)N[C@H]2CCCNC2)c3ccccc3,\"InChI=1S/C17H20N4O2S/c18-17(23)21-13-9-14(11-5-2-1-3-6-11)24-15(13)16(22)20-12-7-4-8-19-10-12/h1-3,5-6,9,12,19H,4,7-8,10H2,(H,20,22)(H3,18,21,23)/t12-/m0/s1\",[N][C][=Branch1][C][=O][N][C][C][=C][Branch2][Ring1][C][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-(carbamoylamino)-5-phenyl-n-[(3s)-piperidin-3-yl]thiophene-2-carboxamide,1.04\nNc1nc(Cl)nc(NCc2ccccc2)n1,\"InChI=1S/C10H10ClN5/c11-8-14-9(12)16-10(15-8)13-6-7-4-2-1-3-5-7/h1-5H,6H2,(H3,12,13,14,15,16)\",[N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][#C],\"6-chloro-n-(phenylmethyl)-1,3,5-triazine-2,4-diamine\",2.26\nCOc1cccc(COCC(O)CN2CCC(CC2)C(=O)N)c1,\"InChI=1S/C17H26N2O4/c1-22-16-4-2-3-13(9-16)11-23-12-15(20)10-19-7-5-14(6-8-19)17(18)21/h2-4,9,14-15,20H,5-8,10-12H2,1H3,(H2,18,21)\",[C][O][C][=C][C][=C][C][Branch2][Ring1][Branch2][C][O][C][C][Branch1][C][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][=C][Ring2][Ring1][Branch1],1-[2-hydroxy-3-[(3-methoxyphenyl)methoxy]propyl]piperidine-4-carboxamide,-0.5\nCOC[C@H](C)Oc1cc(Oc2ccccc2)cc(c1)C(=O)Nc3ccc(cn3)C(=O)O,\"InChI=1S/C23H22N2O6/c1-15(14-29-2)30-19-10-17(11-20(12-19)31-18-6-4-3-5-7-18)22(26)25-21-9-8-16(13-24-21)23(27)28/h3-13,15H,14H2,1-2H3,(H,27,28)(H,24,25,26)/t15-/m0/s1\",[C][O][C][C@H1][Branch1][C][C][O][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Ring2][=C][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O],6-[[3-[(2s)-1-methoxypropan-2-yl]oxy-5-(phenoxy)benzoyl]amino]pyridine-3-carboxylic acid,0.95\nCCOc1ccc(NC(=O)C)cc1,\"InChI=1S/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12)\",[C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2],n-(4-ethoxyphenyl)acetamide,1.5\nOC(=O)Cc1csc(n1)c2ccc(Cl)cc2,\"InChI=1S/C11H8ClNO2S/c12-8-3-1-7(2-4-8)11-13-9(6-16-11)5-10(14)15/h1-4,6H,5H2,(H,14,15)\",[O][C][=Branch1][C][=O][C][C][=C][S][C][=Branch1][Ring2][=N][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"2-[2-(4-chlorophenyl)-1,3-thiazol-4-yl]acetic acid\",-0.22\nOC(=O)c1cccc(c1)c2ccc3c(C(=O)NCC45CC6CC(CC(C6)C4)C5)c(Cl)ccc3n2,\"InChI=1S/C28H27ClN2O3/c29-22-5-7-24-21(4-6-23(31-24)19-2-1-3-20(11-19)27(33)34)25(22)26(32)30-15-28-12-16-8-17(13-28)10-18(9-16)14-28/h1-7,11,16-18H,8-10,12-15H2,(H,30,32)(H,33,34)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Branch1][C][Cl][C][=C][C][Ring2][Ring1][Branch1][=N][Ring2][Ring1][=Branch2],3-[5-(1-adamantylmethylcarbamoyl)-6-chloroquinolin-2-yl]benzoic acid,2.84\nCN1CCN(CC1)C(=O)c2cc3cc(Cl)ccc3[nH]2,\"InChI=1S/C14H16ClN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],(5-chloro-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone,2.4\nOC[C@H](Nc1ncc(Cl)c(Nc2cc([nH]n2)C3CC3)n1)c4ccc(F)cc4,\"InChI=1S/C18H18ClFN6O/c19-13-8-21-18(22-15(9-27)11-3-5-12(20)6-4-11)24-17(13)23-16-7-14(25-26-16)10-1-2-10/h3-8,10,15,27H,1-2,9H2,(H3,21,22,23,24,25,26)/t15-/m0/s1\",[O][C][C@H1][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][Cl][C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],(2r)-2-[[5-chloro-4-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]pyrimidin-2-yl]amino]-2-(4-fluorophenyl)ethanol,3.75\nOC(=O)CNCCNc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C22H30ClN3O3/c23-19-2-1-17(25-4-3-24-12-20(27)28)8-18(19)21(29)26-13-22-9-14-5-15(10-22)7-16(6-14)11-22/h1-2,8,14-16,24-25H,3-7,9-13H2,(H,26,29)(H,27,28)\",[O][C][=Branch1][C][=O][C][N][C][C][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],2-[2-[[3-(1-adamantylmethylcarbamoyl)-4-chlorophenyl]amino]ethylamino]acetic acid,1.94\nCCNC(=O)c1ccc(C)c(c1)N2C=Nc3ccc(cc3C2=O)N4CCN(C)CC4,\"InChI=1S/C23H27N5O2/c1-4-24-22(29)17-6-5-16(2)21(13-17)28-15-25-20-8-7-18(14-19(20)23(28)30)27-11-9-26(3)10-12-27/h5-8,13-15H,4,9-12H2,1-3H3,(H,24,29)\",[C][C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=Branch1][Ring2][=C][Ring1][#Branch1][N][C][=N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],n-ethyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3-yl]benzamide,1.47\nO=C(Nc1nc(cs1)c2ccccc2)c3cccnc3,\"InChI=1S/C15H11N3OS/c19-14(12-7-4-8-16-9-12)18-15-17-13(10-20-15)11-5-2-1-3-6-11/h1-10H,(H,17,18,19)\",[O][=C][Branch2][Ring1][Ring1][N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],\"n-(4-phenyl-1,3-thiazol-2-yl)pyridine-3-carboxamide\",3.62\nCS(=O)(=O)n1c2ccccc2c3cc(NC(=O)CCc4ccncc4)ccc13,\"InChI=1S/C21H19N3O3S/c1-28(26,27)24-19-5-3-2-4-17(19)18-14-16(7-8-20(18)24)23-21(25)9-6-15-10-12-22-13-11-15/h2-5,7-8,10-14H,6,9H2,1H3,(H,23,25)\",[C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch2][Ring1][P],n-(9-methylsulfonylcarbazol-3-yl)-3-pyridin-4-ylpropanamide,3.4\nNc1nnc(Cc2ccc(Cl)cc2)s1,\"InChI=1S/C9H8ClN3S/c10-7-3-1-6(2-4-7)5-8-12-13-9(11)14-8/h1-4H,5H2,(H2,11,13)\",[N][C][=N][N][=C][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][S][Ring1][=N],\"5-[(4-chlorophenyl)methyl]-1,3,4-thiadiazol-2-amine\",2.34\nC[C@H](CO)Nc1nc(SCc2ccccc2F)nc3nc(N)sc13,\"InChI=1S/C15H16FN5OS2/c1-8(6-22)18-12-11-13(19-14(17)24-11)21-15(20-12)23-7-9-4-2-3-5-10(9)16/h2-5,8,22H,6-7H2,1H3,(H3,17,18,19,20,21)/t8-/m1/s1\",[C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][N][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1],\"(2r)-2-[[2-amino-5-[(2-fluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\",3.12\nNc1ccc2ccccc2n1,\"InChI=1S/C9H8N2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H,(H2,10,11)\",[N][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2],quinolin-2-amine,1.7\nO=C1C=C(Oc2c1cccc2c3ccccc3)N4CCOCC4,\"InChI=1S/C19H17NO3/c21-17-13-18(20-9-11-22-12-10-20)23-19-15(7-4-8-16(17)19)14-5-2-1-3-6-14/h1-8,13H,9-12H2\",[O][=C][C][=C][Branch2][Ring1][Ring2][O][C][=C][Ring1][=Branch1][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],2-morpholin-4-yl-8-phenylchromen-4-one,2.9\nCc1c(c2cc(F)ccc2n1CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3,\"InChI=1S/C17H13ClFNO4S/c1-10-17(25(23,24)13-5-2-11(18)3-6-13)14-8-12(19)4-7-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\",[C][C][=C][Branch2][Ring1][Branch1][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][N][Ring1][#Branch2][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[3-(4-chlorophenyl)sulfonyl-5-fluoro-2-methylindol-1-yl]acetic acid,-0.16\nNS(=O)(=O)c1cc2c(NC(NS2(=O)=O)C(Cl)Cl)cc1Cl,\"InChI=1S/C8H8Cl3N3O4S2/c9-3-1-4-6(2-5(3)19(12,15)16)20(17,18)14-8(13-4)7(10)11/h1-2,7-8,13-14H,(H2,12,15,16)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][C][N][C][Branch1][=Branch2][N][S][Ring1][=Branch1][=Branch1][C][=O][=O][C][Branch1][C][Cl][Cl][C][=C][Ring1][#C][Cl],\"6-chloro-3-(dichloromethyl)-1,1-dioxo-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\",0.37\nO=C(NCCCCc1ccccc1)c2ccccc2,\"InChI=1S/C17H19NO/c19-17(16-12-5-2-6-13-16)18-14-8-7-11-15-9-3-1-4-10-15/h1-6,9-10,12-13H,7-8,11,14H2,(H,18,19)\",[O][=C][Branch1][=C][N][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-(4-phenylbutyl)benzamide,3.8\nNC(=O)C1CCCCC1,\"InChI=1S/C7H13NO/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2,(H2,8,9)\",[N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][=Branch1],cyclohexanecarboxamide,0.9\nCN(C)c1ncnc2nc[nH]c12,\"InChI=1S/C7H9N5/c1-12(2)7-5-6(9-3-8-5)10-4-11-7/h3-4H,1-2H3,(H,8,9,10,11)\",[C][N][Branch1][C][C][C][=N][C][=N][C][N][=C][NH1][C][Ring1][=Branch2][=Ring1][Branch1],\"n,n-dimethyl-7h-purin-6-amine\",0.95\nCOc1ccc(cc1)S(=O)(=O)Nc2ccccn2,\"InChI=1S/C12H12N2O3S/c1-17-10-5-7-11(8-6-10)18(15,16)14-12-4-2-3-9-13-12/h2-9H,1H3,(H,13,14)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1],4-methoxy-n-pyridin-2-ylbenzenesulfonamide,0.87\nCOc1ccc(NC(=O)C=C)cc1,\"InChI=1S/C10H11NO2/c1-3-10(12)11-8-4-6-9(13-2)7-5-8/h3-7H,1H2,2H3,(H,11,12)\",[C][O][C][=C][C][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][O],n-(4-methoxyphenyl)prop-2-enamide,1.68\nCn1c(Nc2ccc(cc2)C(F)(F)F)nc3cc(Oc4ccnc(c4)c5ncc([nH]5)C(F)(F)F)ccc13,\"InChI=1S/C24H16F6N6O/c1-36-19-7-6-15(10-17(19)34-22(36)33-14-4-2-13(3-5-14)23(25,26)27)37-16-8-9-31-18(11-16)21-32-12-20(35-21)24(28,29)30/h2-12H,1H3,(H,32,35)(H,33,34)\",[C][N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=N][C][=C][C][Branch2][Ring1][=N][O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=N][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][C][=C][Ring2][Ring2][Ring2][Ring2][Ring1][=Branch1],1-methyl-5-[2-[4-(trifluoromethyl)-3h-imidazol-2-yl]pyridin-4-yl]oxy-n-[4-(trifluoromethyl)phenyl]benzimidazol-2-amine,3.45\nNc1nc(ns1)c2ccccc2,\"InChI=1S/C8H7N3S/c9-8-10-7(11-12-8)6-4-2-1-3-5-6/h1-5H,(H2,9,10,11)\",[N][C][=N][C][=Branch1][Branch1][=N][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-phenyl-1,2,4-thiadiazol-5-amine\",2.2\nCC(N(O)C(=O)N)c1cc2ccccc2s1,\"InChI=1S/C11H12N2O2S/c1-7(13(15)11(12)14)10-6-8-4-2-3-5-9(8)16-10/h2-7,15H,1H3,(H2,12,14)\",[C][C][Branch1][#Branch2][N][Branch1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2],1-[1-(1-benzothiophen-2-yl)ethyl]-1-hydroxyurea,2.05\nCc1onc(NC(=O)CSc2nc(C)cc(C)n2)c1,\"InChI=1S/C12H14N4O2S/c1-7-4-8(2)14-12(13-7)19-6-11(17)15-10-5-9(3)18-16-10/h4-5H,6H2,1-3H3,(H,15,16,17)\",[C][C][O][N][=C][Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][S][C][=N][C][Branch1][C][C][=C][C][Branch1][C][C][=N][Ring1][Branch2][C][=Ring2][Ring1][C],\"2-(4,6-dimethylpyrimidin-2-yl)sulfanyl-n-(5-methyl-1,2-oxazol-3-yl)acetamide\",1.52\nCN1C(=O)N(C)c2ncn(CC(O)CO)c2C1=O,\"InChI=1S/C10H14N4O4/c1-12-8-7(9(17)13(2)10(12)18)14(5-11-8)3-6(16)4-15/h5-6,15-16H,3-4H2,1-2H3\",[C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][Branch2][C][C][Branch1][C][O][C][O][C][=Ring1][#Branch2][C][Ring1][S][=O],\"7-(2,3-dihydroxypropyl)-1,3-dimethylpurine-2,6-dione\",-1.25\nCN1C(=O)CC(C)(CCc2cccc(c2)c3ccccc3)N=C1N,\"InChI=1S/C20H23N3O/c1-20(14-18(24)23(2)19(21)22-20)12-11-15-7-6-10-17(13-15)16-8-4-3-5-9-16/h3-10,13H,11-12,14H2,1-2H3,(H2,21,22)\",[C][N][C][=Branch1][C][=O][C][C][Branch1][C][C][Branch2][Ring1][Branch1][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring2][Ring1][=Branch1][N],\"2-amino-3,6-dimethyl-6-[2-(3-phenylphenyl)ethyl]-5h-pyrimidin-4-one\",2.03\nCOc1cc(ccc1Cc2cn(C)c3ccc(cc23)C(=O)NCCc4ccccc4)C(=O)NS(=O)(=O)c5ccccc5C,\"InChI=1S/C34H33N3O5S/c1-23-9-7-8-12-32(23)43(40,41)36-34(39)27-14-13-25(31(21-27)42-3)19-28-22-37(2)30-16-15-26(20-29(28)30)33(38)35-18-17-24-10-5-4-6-11-24/h4-16,20-22H,17-19H2,1-3H3,(H,35,38)(H,36,39)\",[C][O][C][=C][C][=Branch2][Ring2][Branch2][=C][C][=C][Ring1][=Branch1][C][C][=C][N][Branch1][C][C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C],3-[[2-methoxy-4-[(2-methylphenyl)sulfonylcarbamoyl]phenyl]methyl]-1-methyl-n-(2-phenylethyl)indole-5-carboxamide,2.51\nCc1ccc(cc1)c2nn(c3ncnc(N)c23)C(C)(C)C,\"InChI=1S/C16H19N5/c1-10-5-7-11(8-6-10)13-12-14(17)18-9-19-15(12)21(20-13)16(2,3)4/h5-9H,1-4H3,(H2,17,18,19)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][Branch1][=C][C][=N][C][=N][C][Branch1][C][N][=C][Ring1][#Branch2][Ring1][#Branch1][C][Branch1][C][C][Branch1][C][C][C],\"1-tert-butyl-3-(4-methylphenyl)pyrazolo[4,5-e]pyrimidin-4-amine\",4.1\nCOc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC4CCN(CC(=O)N)CC4,\"InChI=1S/C22H23ClFN5O3/c1-31-18-10-17-14(9-19(18)32-13-5-7-29(8-6-13)11-20(25)30)22(27-12-26-17)28-16-4-2-3-15(23)21(16)24/h2-4,9-10,12-13H,5-8,11H2,1H3,(H2,25,30)(H,26,27,28)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][#Branch1][C][C][=Branch1][C][=O][N][C][C][Ring1][#Branch2],2-[4-[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]acetamide,3.1\nNC(=O)c1ccc(Br)cc1,\"InChI=1S/C7H6BrNO/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H2,9,10)\",[N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],4-bromobenzamide,1.75\nN[C@H](Cc1c[nH]c2ccccc12)C(=O)O,\"InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m1/s1\",[N][C@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][O],(2r)-2-amino-3-(1h-indol-3-yl)propanoic acid,-0.92\nCC(C)CN1C(=O)N(C)C(=O)c2c(SCCCO)c(Cc3ccccc3C(F)(F)F)sc12,\"InChI=1S/C22H25F3N2O3S2/c1-13(2)12-27-20-17(19(29)26(3)21(27)30)18(31-10-6-9-28)16(32-20)11-14-7-4-5-8-15(14)22(23,24)25/h4-5,7-8,13,28H,6,9-12H2,1-3H3\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][C][Branch1][=Branch1][S][C][C][C][O][=C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][S][C][Ring2][Ring1][N][=Ring2][Ring1][Branch1],\"5-(3-hydroxypropylsulfanyl)-3-methyl-1-(2-methylpropyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\",4.05\nClc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4cccs4)C3=O,\"InChI=1S/C16H10ClN3O3S/c17-8-3-4-10-11(6-8)18-13-12(14(10)21)16(23)20(19-15(13)22)7-9-2-1-5-24-9/h1-6H,7H2,(H,18,21)(H,19,22)\",[Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][=Branch2][C][C][=C][C][=C][S][Ring1][Branch1][C][Ring1][S][=O],\"7-chloro-2-(thiophen-2-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",1.52\nNc1[nH]ncc1S(=O)(=O)c2ccccc2,\"InChI=1S/C9H9N3O2S/c10-9-8(6-11-12-9)15(13,14)7-4-2-1-3-5-7/h1-6H,(H3,10,11,12)\",[N][C][NH1][N][=C][C][=Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],4-phenylsulfonyl-2h-pyrazol-3-amine,1.1\nCCn1c2ccccc2c3cc(NC(=O)CCc4ccncc4)ccc13,\"InChI=1S/C22H21N3O/c1-2-25-20-6-4-3-5-18(20)19-15-17(8-9-21(19)25)24-22(26)10-7-16-11-13-23-14-12-16/h3-6,8-9,11-15H,2,7,10H2,1H3,(H,24,26)\",[C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch2][Ring1][P],n-(9-ethylcarbazol-3-yl)-3-pyridin-4-ylpropanamide,3.75\nFc1ccc2cn[nH]c2c1,\"InChI=1S/C7H5FN2/c8-6-2-1-5-4-9-10-7(5)3-6/h1-4H,(H,9,10)\",[F][C][=C][C][=C][C][=N][NH1][C][Ring1][Branch1][=C][Ring1][=Branch2],6-fluoro-1h-indazole,2.3\nCCC1(CCC(=O)NC1=O)c2ccc(N)cc2,\"InChI=1S/C13H16N2O2/c1-2-13(8-7-11(16)15-12(13)17)9-3-5-10(14)6-4-9/h3-6H,2,7-8,14H2,1H3,(H,15,16,17)\",[C][C][C][Branch1][N][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],\"3-(4-aminophenyl)-3-ethylpiperidine-2,6-dione\",0.6\nOC(=O)CCCc1ccc(cc1)N(CCCl)CCCl,\"InChI=1S/C14H19Cl2NO2/c15-8-10-17(11-9-16)13-6-4-12(5-7-13)2-1-3-14(18)19/h4-7H,1-3,8-11H2,(H,18,19)\",[O][C][=Branch1][C][=O][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][Ring2][C][C][Cl][C][C][Cl],4-[4-[bis(2-chloroethyl)amino]phenyl]butanoic acid,1.47\nCC(C)N=C1C=C2N(c3ccc(Cl)cc3)c4ccccc4N=C2C=C1Nc5ccc(Cl)cc5,\"InChI=1S/C27H22Cl2N4/c1-17(2)30-24-16-27-25(15-23(24)31-20-11-7-18(28)8-12-20)32-22-5-3-4-6-26(22)33(27)21-13-9-19(29)10-14-21/h3-17,31H,1-2H3\",[C][C][Branch1][C][C][N][=C][C][=C][N][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"n,5-bis(4-chlorophenyl)-3-propan-2-yliminophenazin-2-amine\",3.17\nCN(C)CC(O)COc1ccc(Nc2cc(Nc3cc(Cl)ccc3Cl)ncn2)cc1,\"InChI=1S/C21H23Cl2N5O2/c1-28(2)11-16(29)12-30-17-6-4-15(5-7-17)26-20-10-21(25-13-24-20)27-19-9-14(22)3-8-18(19)23/h3-10,13,16,29H,11-12H2,1-2H3,(H2,24,25,26,27)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][Cl][=N][C][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1],\"1-[4-[[6-[(2,5-dichlorophenyl)amino]pyrimidin-4-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\",2.6\nCN1CCN(CC1)c2ccc(Nc3ncc(C)c(Nc4cccc(c4)S(=O)(=O)NC(C)(C)C)n3)cc2,\"InChI=1S/C26H35N7O2S/c1-19-18-27-25(29-20-9-11-22(12-10-20)33-15-13-32(5)14-16-33)30-24(19)28-21-7-6-8-23(17-21)36(34,35)31-26(2,3)4/h6-12,17-18,31H,13-16H2,1-5H3,(H2,27,28,29,30)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring2][N][N][C][=N][C][=C][Branch1][C][C][C][Branch2][Ring1][N][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C][=N][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][=N],n-tert-butyl-3-[[5-methyl-2-[[4-(4-methylpiperazin-1-yl)phenyl]amino]pyrimidin-4-yl]amino]benzenesulfonamide,2.84\nNS(=O)(=O)c1cc(Cl)c(Cl)c(c1)S(=O)(=O)N,\"InChI=1S/C6H6Cl2N2O4S2/c7-4-1-3(15(9,11)12)2-5(6(4)8)16(10,13)14/h1-2H,(H2,9,11,12)(H2,10,13,14)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N],\"4,5-dichlorobenzene-1,3-disulfonamide\",0.92\nFc1ccc(cc1)c2cn3ccccc3n2,InChI=1S/C13H9FN2/c14-11-6-4-10(5-7-11)12-9-16-8-2-1-3-13(16)15-12/h1-9H,[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2],\"2-(4-fluorophenyl)imidazo[1,2-a]pyridine\",3.1\nFc1ccc(CC2=NNC(=O)c3ccccc23)cc1N4C(=O)CCC4=O,\"InChI=1S/C19H14FN3O3/c20-14-6-5-11(10-16(14)23-17(24)7-8-18(23)25)9-15-12-3-1-2-4-13(12)19(26)22-21-15/h1-6,10H,7-9H2,(H,22,26)\",[F][C][=C][C][=C][Branch2][Ring1][Ring1][C][C][=N][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][=O],\"1-[2-fluoro-5-[(4-oxo-3h-phthalazin-1-yl)methyl]phenyl]pyrrolidine-2,5-dione\",1\nCN(C)c1cccc2c(cccc12)S(=O)(=O)N(C)CC(=O)O,\"InChI=1S/C15H18N2O4S/c1-16(2)13-8-4-7-12-11(13)6-5-9-14(12)22(20,21)17(3)10-15(18)19/h4-9H,10H2,1-3H3,(H,18,19)\",[C][N][Branch1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][Branch1][C][C][C][C][=Branch1][C][=O][O],2-[(5-dimethylaminonaphthalen-1-yl)sulfonyl-methylamino]acetic acid,-1.45\nCc1cc(on1)c2ccc(cc2F)N3C[C@H](Cn4ccnn4)OC3=O,\"InChI=1S/C16H14FN5O3/c1-10-6-15(25-19-10)13-3-2-11(7-14(13)17)22-9-12(24-16(22)23)8-21-5-4-18-20-21/h2-7,12H,8-9H2,1H3/t12-/m0/s1\",[C][C][C][=C][Branch1][Branch1][O][N][=Ring1][Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][N][C][C@H1][Branch1][=Branch2][C][N][C][=C][N][=N][Ring1][Branch1][O][C][Ring1][O][=O],\"(5r)-3-[3-fluoro-4-(3-methyl-1,2-oxazol-5-yl)phenyl]-5-(triazol-1-ylmethyl)-1,3-oxazolidin-2-one\",1.99\nCOc1ccnc(NC2CCN(CC2)C(=O)c3ccccc3)c1,\"InChI=1S/C18H21N3O2/c1-23-16-7-10-19-17(13-16)20-15-8-11-21(12-9-15)18(22)14-5-3-2-4-6-14/h2-7,10,13,15H,8-9,11-12H2,1H3,(H,19,20)\",[C][O][C][=C][C][=N][C][Branch2][Ring1][Branch2][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring2][Ring1][Branch1],[4-[(4-methoxypyridin-2-yl)amino]piperidin-1-yl]-phenylmethanone,2.06\nNc1c(cnn1c2ccc(F)cc2)C(=O)c3cccc(OC[C@H](O)CO)c3,\"InChI=1S/C19H18FN3O4/c20-13-4-6-14(7-5-13)23-19(21)17(9-22-23)18(26)12-2-1-3-16(8-12)27-11-15(25)10-24/h1-9,15,24-25H,10-11,21H2/t15-/m1/s1\",[N][C][=C][Branch1][P][C][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][=Branch2][O][C][C@H1][Branch1][C][O][C][O][=C][Ring1][N],\"[5-amino-1-(4-fluorophenyl)pyrazol-4-yl]-[3-[(2r)-2,3-dihydroxypropoxy]phenyl]methanone\",1.94\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCN4CCN(C)CC4,\"InChI=1S/C22H25ClFN5O2/c1-28-5-7-29(8-6-28)9-10-31-21-12-16-19(13-20(21)30-2)25-14-26-22(16)27-15-3-4-18(24)17(23)11-15/h3-4,11-14H,5-10H2,1-2H3,(H,25,26,27)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],n-(3-chloro-4-fluorophenyl)-7-methoxy-6-[2-(4-methylpiperazin-1-yl)ethoxy]quinazolin-4-amine,3.3\nO=C1NCCc2[nH]c(cc12)c3ccncc3,\"InChI=1S/C12H11N3O/c16-12-9-7-11(8-1-4-13-5-2-8)15-10(9)3-6-14-12/h1-2,4-5,7,15H,3,6H2,(H,14,16)\",[O][=C][N][C][C][C][NH1][C][=Branch1][#Branch1][=C][C][Ring1][=Branch2][=Ring1][Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1],\"2-pyridin-4-yl-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one\",1.49\nCOc1cc(ccc1OCCN2CCCC2)N3C=Nc4cc(sc4C3=O)c5ccc(Cl)cc5,\"InChI=1S/C25H24ClN3O3S/c1-31-22-14-19(8-9-21(22)32-13-12-28-10-2-3-11-28)29-16-27-20-15-23(33-24(20)25(29)30)17-4-6-18(26)7-5-17/h4-9,14-16H,2-3,10-13H2,1H3\",[C][O][C][=C][C][=Branch1][S][=C][C][=C][Ring1][=Branch1][O][C][C][N][C][C][C][C][Ring1][Branch1][N][C][=N][C][C][=C][Branch1][=Branch2][S][C][=Ring1][Branch1][C][Ring1][=Branch2][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"6-(4-chlorophenyl)-3-[3-methoxy-4-(2-pyrrolidin-1-ylethoxy)phenyl]thieno[2,3-e]pyrimidin-4-one\",2.74\nCN1CCc2c(NC(=O)Cc3ccccc3)c4ccccc4nc12,\"InChI=1S/C20H19N3O/c1-23-12-11-16-19(15-9-5-6-10-17(15)21-20(16)23)22-18(24)13-14-7-3-2-4-8-14/h2-10H,11-13H2,1H3,(H,21,22,24)\",[C][N][C][C][C][=C][Branch1][#C][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring2][Ring1][#Branch1][Ring2][Ring1][Ring2],\"n-(1-methyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-yl)-2-phenylacetamide\",2.8\nCc1c[nH]c(\\C=C\\2/C(=O)Nc3ccccc23)c1CCC(=O)O,\"InChI=1S/C17H16N2O3/c1-10-9-18-15(11(10)6-7-16(20)21)8-13-12-4-2-3-5-14(12)19-17(13)22/h2-5,8-9,18H,6-7H2,1H3,(H,19,22)(H,20,21)/b13-8-\",[C][C][=C][NH1][C][Branch2][Ring1][C][\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][\\-Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][C][C][=Branch1][C][=O][O],\"3-[4-methyl-2-[(2-oxo-1h-indol-3-ylidene)methyl]-1h-pyrrol-3-yl]propanoic acid\n3-[4-methyl-2-[(z)-(2-oxo-1h-indol-3-ylidene)methyl]-1h-pyrrol-3-yl]propanoic acid\",1.2\nClc1cnc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)N5CCNCC5,\"InChI=1S/C21H29ClN4O/c22-18-12-24-19(26-3-1-23-2-4-26)8-17(18)20(27)25-13-21-9-14-5-15(10-21)7-16(6-14)11-21/h8,12,14-16,23H,1-7,9-11,13H2,(H,25,27)\",[Cl][C][=C][N][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][C][C][N][C][C][Ring1][=Branch1],n-(1-adamantylmethyl)-5-chloro-2-piperazin-1-ylpyridine-4-carboxamide,2.09\nCC1=C(N2[C@H](SC1)[C@H](NC(=O)[C@H](N)c3ccc(O)cc3)C2=O)C(=O)O,\"InChI=1S/C16H17N3O5S/c1-7-6-25-15-11(14(22)19(15)12(7)16(23)24)18-13(21)10(17)8-2-4-9(20)5-3-8/h2-5,10-11,15,20H,6,17H2,1H3,(H,18,21)(H,23,24)/t10-,11-,15-/m1/s1\",[C][C][=C][Branch2][Ring2][=Branch1][N][C@H1][Branch1][Branch1][S][C][Ring1][=Branch1][C@H1][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C@H1][Branch1][C][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Ring2][Ring1][C][=O][C][=Branch1][C][=O][O],\"(6r,7r)-7-[[(2r)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid\",-0.86\nCN(C)CCOC(c1ccccc1)c2ccccc2C,\"InChI=1S/C18H23NO/c1-15-9-7-8-12-17(15)18(20-14-13-19(2)3)16-10-5-4-6-11-16/h4-12,18H,13-14H2,1-3H3\",[C][N][Branch1][C][C][C][C][O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C],\"n,n-dimethyl-2-[(2-methylphenyl)-phenylmethoxy]ethanamine\",1.47\nCCOc1ccc2nc(NC(=O)CC)sc2c1,\"InChI=1S/C12H14N2O2S/c1-3-11(15)14-12-13-9-6-5-8(16-4-2)7-10(9)17-12/h5-7H,3-4H2,1-2H3,(H,13,14,15)\",[C][C][O][C][=C][C][=C][N][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][C][S][C][Ring1][#Branch2][=C][Ring1][=C],\"n-(6-ethoxy-1,3-benzothiazol-2-yl)propanamide\",3.4\nO=C(NCc1ccccn1)c2ccc(Oc3ccccc3)cc2,\"InChI=1S/C19H16N2O2/c22-19(21-14-16-6-4-5-13-20-16)15-9-11-18(12-10-15)23-17-7-2-1-3-8-17/h1-13H,14H2,(H,21,22)\",[O][=C][Branch1][O][N][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N],4-(phenoxy)-n-(pyridin-2-ylmethyl)benzamide,2.7\nCN1CCN(CC1)S(=O)(=O)c2ccc(cc2F)c3cnc(N)c(n3)C(=O)Nc4cccnc4,\"InChI=1S/C21H22FN7O3S/c1-28-7-9-29(10-8-28)33(31,32)18-5-4-14(11-16(18)22)17-13-25-20(23)19(27-17)21(30)26-15-3-2-6-24-12-15/h2-6,11-13H,7-10H2,1H3,(H2,23,25)(H,26,30)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1],3-amino-6-[3-fluoro-4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-pyridin-3-ylpyrazine-2-carboxamide,2.66\nCOc1ccccc1C2=COc3cc(O)ccc3C2=O,\"InChI=1S/C16H12O4/c1-19-14-5-3-2-4-11(14)13-9-20-15-8-10(17)6-7-12(15)16(13)18/h2-9,17H,1H3\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][C][Ring1][O][=O],7-hydroxy-3-(2-methoxyphenyl)chromen-4-one,2.55\nFc1ccc(cc1F)N2C=CN=C(SCC(=O)NC3CCCC3)C2=O,\"InChI=1S/C17H17F2N3O2S/c18-13-6-5-12(9-14(13)19)22-8-7-20-16(17(22)24)25-10-15(23)21-11-3-1-2-4-11/h5-9,11H,1-4,10H2,(H,21,23)\",[F][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][N][C][=C][N][=C][Branch1][#C][S][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][Ring1][S][=O],\"n-cyclopentyl-2-[4-(3,4-difluorophenyl)-3-oxopyrazin-2-yl]sulfanylacetamide\",2\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3ccccn3)C(=O)C(F)(F)F,\"InChI=1S/C26H25F3N4O5/c1-16(2)22(23(35)26(27,28)29)32-21(34)14-33-20(17-8-4-3-5-9-17)12-11-19(24(33)36)31-25(37)38-15-18-10-6-7-13-30-18/h3-13,16,22H,14-15H2,1-2H3,(H,31,37)(H,32,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"pyridin-2-ylmethyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamate\",1.91\nCOc1ccc(cc1)C(=O)CS(=O)(=O)c2ccccc2,\"InChI=1S/C15H14O4S/c1-19-13-9-7-12(8-10-13)15(16)11-20(17,18)14-5-3-2-4-6-14/h2-10H,11H2,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],1-(4-methoxyphenyl)-2-phenylsulfonylethanone,1.96\nCN(C)CC\\C=C\\1/c2ccccc2Sc3ccc(Cl)cc13,\"InChI=1S/C18H18ClNS/c1-20(2)11-5-7-14-15-6-3-4-8-17(15)21-18-10-9-13(19)12-16(14)18/h3-4,6-10,12H,5,11H2,1-2H3/b14-7+\",[C][N][Branch1][C][C][C][C][\\C][=C][/C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][\\-Ring1][#C][Ring1][#Branch1],\"(3e)-3-(2-chlorothioxanthen-9-ylidene)-n,n-dimethylpropan-1-amine\n3-(2-chlorothioxanthen-9-ylidene)-n,n-dimethylpropan-1-amine\",3.42\nClc1ccc(cc1)C2(CCC2)C(=O)Nc3oc(nn3)C(=O)Nc4ccc(cc4)N5CCOCC5,\"InChI=1S/C24H24ClN5O4/c25-17-4-2-16(3-5-17)24(10-1-11-24)22(32)27-23-29-28-21(34-23)20(31)26-18-6-8-19(9-7-18)30-12-14-33-15-13-30/h2-9H,1,10-15H2,(H,26,31)(H,27,29,32)\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=Branch1][C][=O][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"5-[[1-(4-chlorophenyl)cyclobutanecarbonyl]amino]-n-(4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\",3.2\nCC(COc1ccccc1)NC(C)C(O)c2ccc(O)cc2,\"InChI=1S/C18H23NO3/c1-13(12-22-17-6-4-3-5-7-17)19-14(2)18(21)15-8-10-16(20)11-9-15/h3-11,13-14,18-21H,12H2,1-2H3\",[C][C][Branch1][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][C][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],4-[1-hydroxy-2-[1-(phenoxy)propan-2-ylamino]propyl]phenol,0.56\nCc1ccc2c(c1)c(Sc3ccccc3)c(CC(=O)O)n2C,\"InChI=1S/C18H17NO2S/c1-12-8-9-15-14(10-12)18(16(19(15)2)11-17(20)21)22-13-6-4-3-5-7-13/h3-10H,11H2,1-2H3,(H,20,21)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][#Branch2][S][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][Ring1][P][C],\"2-(1,5-dimethyl-3-phenylsulfanylindol-2-yl)acetic acid\",1.74\nO=C(N1CCNCC1)c2cc3ccccc3[nH]2,\"InChI=1S/C13H15N3O/c17-13(16-7-5-14-6-8-16)12-9-10-3-1-2-4-11(10)15-12/h1-4,9,14-15H,5-8H2\",[O][=C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],1h-indol-2-yl-piperazin-1-ylmethanone,0.6\nCN[C@@H](C)C(=O)N[C@@H](C1CCCCC1)C(=O)N2CC[C@H]3CCN(CCc4ccccc4)C[C@@H]23,\"InChI=1S/C27H42N4O2/c1-20(28-2)26(32)29-25(23-11-7-4-8-12-23)27(33)31-18-15-22-14-17-30(19-24(22)31)16-13-21-9-5-3-6-10-21/h3,5-6,9-10,20,22-25,28H,4,7-8,11-19H2,1-2H3,(H,29,32)/t20-,22+,24+,25-/m0/s1\",[C][N][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C@H1][C][C][N][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C@@H1][Ring1][P][Ring1][=C],\"(2s)-n-[(1s)-2-[(3ar,7as)-6-(2-phenylethyl)-3,3a,4,5,7,7a-hexahydro-2h-pyrrolo[2,3-c]pyridin-1-yl]-1-cyclohexyl-2-oxoethyl]-2-methylaminopropanamide\",2.47\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccc(F)cc2)N)C(=O)C(F)(F)F,\"InChI=1S/C18H18F4N4O3/c1-9(2)14(15(28)18(20,21)22)25-13(27)8-26-16(24-7-12(23)17(26)29)10-3-5-11(19)6-4-10/h3-7,9,14H,8,23H2,1-2H3,(H,25,27)\",[C][C][Branch1][C][C][C][Branch2][Ring1][S][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][P][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[5-amino-2-(4-fluorophenyl)-6-oxopyrimidin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.05\nCc1cc(Nc2ccnc(NCc3onc(c3)C4CC4)n2)n[nH]1,\"InChI=1S/C15H17N7O/c1-9-6-14(21-20-9)18-13-4-5-16-15(19-13)17-8-11-7-12(22-23-11)10-2-3-10/h4-7,10H,2-3,8H2,1H3,(H3,16,17,18,19,20,21)\",[C][C][=C][C][Branch2][Ring1][N][N][C][=C][C][=N][C][Branch1][P][N][C][C][O][N][=C][Branch1][Ring2][C][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][=N][NH1][Ring2][Ring1][=Branch1],\"n-[(3-cyclopropyl-1,2-oxazol-5-yl)methyl]-n'-(5-methyl-1h-pyrazol-3-yl)pyrimidine-2,4-diamine\",2.5\nCOc1ccc2CCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1,\"InChI=1S/C25H31N5O4/c1-33-20-5-2-17-3-7-24(32)30(21(17)14-20)13-12-29-10-8-18(9-11-29)26-15-19-4-6-22-25(27-19)28-23(31)16-34-22/h2,4-6,14,18,26H,3,7-13,15-16H2,1H3,(H,27,28,31)\",[C][O][C][=C][C][=C][C][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S],\"6-[[[1-[2-(7-methoxy-2-oxo-3,4-dihydroquinolin-1-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",0.66\nCC[C@H](C)[C@H](N)C1=N[C@@H](CS1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(=O)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H]2CCCCNC(=O)[C@H](CC(=O)N)NC(=O)[C@@H](CC(=O)O)NC(=O)[C@H](Cc3cnc[nH]3)NC(=O)[C@@H](Cc4ccccc4)NC(=O)[C@@H](NC(=O)[C@@H](CCCN)NC2=O)[C@@H](C)CC,\"InChI=1S/C66H103N17O16S/c1-9-35(6)52(69)66-81-48(32-100-66)63(97)76-43(26-34(4)5)59(93)74-42(22-23-50(85)86)58(92)83-53(36(7)10-2)64(98)75-40-20-15-16-25-71-55(89)46(29-49(68)84)78-62(96)47(30-51(87)88)79-61(95)45(28-39-31-70-33-72-39)77-60(94)44(27-38-18-13-12-14-19-38)80-65(99)54(37(8)11-3)82-57(91)41(21-17-24-67)73-56(40)90/h12-14,18-19,31,33-37,40-48,52-54H,9-11,15-17,20-30,32,67,69H2,1-8H3,(H2,68,84)(H,70,72)(H,71,89)(H,73,90)(H,74,93)(H,75,98)(H,76,97)(H,77,94)(H,78,96)(H,79,95)(H,80,99)(H,82,91)(H,83,92)(H,85,86)(H,87,88)/t35-,36-,37-,40-,41+,42+,43-,44+,45-,46-,47+,48-,52-,53-,54-/m0/s1\",[C][C][C@H1][Branch1][C][C][C@H1][Branch1][C][N][C][=N][C@@H1][Branch1][Branch1][C][S][Ring1][Branch1][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C@H1][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch1][C@@H1][Branch1][C][C][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][C][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][=Branch1][C][=O][N][N][C][=Branch1][C][=O][C@@H1][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][C][=Branch1][C][=O][C@H1][Branch1][=Branch2][C][C][=C][N][=C][NH1][Ring1][Branch1][N][C][=Branch1][C][=O][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C@@H1][Branch2][Ring1][Ring1][N][C][=Branch1][C][=O][C@@H1][Branch1][Branch1][C][C][C][N][N][C][Ring2][Branch1][Branch2][=O][C@@H1][Branch1][C][C][C][C],\"(4r)-4-[[(2s)-2-[[(4r)-2-[(1s,2s)-1-amino-2-methylbutyl]4,5-dihydro-1,3-thiazole-4-carbonyl]amino]-4-methylpentanoyl]amino]-5-[[(2s,3s)-1-[[(3s,6r,9s,12r,15s,18r,21s)-3-(2-amino-2-oxoethyl)-18-(3-aminopropyl)-15-[(2s)-butan-2-yl]-6-(carboxymethyl)-9-(3h-imidazol-4-ylmethyl)-2,5,8,11,14,17,20-heptaoxo-12-(phenylmethyl)-1,4,7,10,13,16,19-heptazacyclopentacos-21-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-5-oxopentanoic acid\",-0.46\nOC(=O)c1[nH]c2cc(Cl)cc(Cl)c2c1\\C=C\\C(=O)Nc3ccccc3,\"InChI=1S/C18H12Cl2N2O3/c19-10-8-13(20)16-12(17(18(24)25)22-14(16)9-10)6-7-15(23)21-11-4-2-1-3-5-11/h1-9,22H,(H,21,23)(H,24,25)/b7-6+\",[O][C][=Branch1][C][=O][C][NH1][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=Ring1][O][\\C][=C][\\C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4,6-dichloro-3-[(e)-3-oxo-3-(phenylamino)prop-1-enyl]-1h-indole-2-carboxylic acid\",1.52\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3cccnc3)C(=O)C(F)(F)F,\"InChI=1S/C26H26F3N5O4/c1-16(2)22(23(36)26(27,28)29)33-21(35)15-34-20(18-8-4-3-5-9-18)11-10-19(24(34)37)32-25(38)31-14-17-7-6-12-30-13-17/h3-13,16,22H,14-15H2,1-2H3,(H,33,35)(H2,31,32,38)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-6-phenyl-3-(pyridin-3-ylmethylcarbamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.84\nCC[C@H](NC(=O)c1c([S+]([O-])CC)c(nc2ccccc12)c3ccccc3)c4ccccc4,\"InChI=1S/C27H26N2O2S/c1-3-22(19-13-7-5-8-14-19)29-27(30)24-21-17-11-12-18-23(21)28-25(26(24)32(31)4-2)20-15-9-6-10-16-20/h5-18,22H,3-4H2,1-2H3,(H,29,30)/t22-,32?/m0/s1\",[C][C][C@H1][Branch2][Ring2][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][S+1][Branch1][C][O-1][C][C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-ethylsulfinyl-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,3.45\nNc1n[nH]c2c(Cl)cccc12,\"InChI=1S/C7H6ClN3/c8-5-3-1-2-4-6(5)10-11-7(4)9/h1-3H,(H3,9,10,11)\",[N][C][=N][NH1][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch2][Ring1][#Branch1],7-chloro-1h-indazol-3-amine,1.7\nOc1ccc(cc1)C2=Cc3ccc(O)cc3OC2,\"InChI=1S/C15H12O3/c16-13-4-1-10(2-5-13)12-7-11-3-6-14(17)8-15(11)18-9-12/h1-8,16-17H,9H2\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O],3-(4-hydroxyphenyl)-2h-chromen-7-ol,3.8\nOB(O)c1ccccc1C=O,\"InChI=1S/C7H7BO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5,10-11H\",[O][B][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=O],(2-formylphenyl)boronic acid,0.83\nO=C(N1CC(=O)Nc2ccccc12)c3occc3,\"InChI=1S/C13H10N2O3/c16-12-8-15(13(17)11-6-3-7-18-11)10-5-2-1-4-9(10)14-12/h1-7H,8H2,(H,14,16)\",[O][=C][Branch2][Ring1][C][N][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][O][C][=C][C][=Ring1][Branch1],\"4-(furan-2-carbonyl)-1,3-dihydroquinoxalin-2-one\",1.21\nCCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cc(F)c(F)c(F)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H37F3N2O5S2/c1-4-37(31(38)19-22-5-9-26(10-6-22)43(2,39)40)25-13-16-36(17-14-25)18-15-28(24-20-29(33)32(35)30(34)21-24)23-7-11-27(12-8-23)44(3,41)42/h5-12,20-21,25,28H,4,13-19H2,1-3H3/t28-/m1/s1\",[C][C][N][Branch2][Branch1][=Branch1][C][C][C][N][Branch2][Ring2][#Branch2][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][=Branch2][C][C][Ring2][Ring1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],\"n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[(3r)-3-(4-methylsulfonylphenyl)-3-(3,4,5-trifluorophenyl)propyl]piperidin-4-yl]acetamide\",2.55\nO=C1C=CN=C2C=CC=CN12,InChI=1S/C8H6N2O/c11-8-4-5-9-7-3-1-2-6-10(7)8/h1-6H,[O][=C][C][=C][N][=C][C][=C][C][=C][N][Ring1][#Branch2][Ring1][=Branch1],\"pyrido[2,1-b]pyrimidin-4-one\",0.2\nCCCC(=O)Nc1ccc(Cl)c(c1)c2oc3cccnc3n2,\"InChI=1S/C16H14ClN3O2/c1-2-4-14(21)19-10-6-7-12(17)11(9-10)16-20-15-13(22-16)5-3-8-18-15/h3,5-9H,2,4H2,1H3,(H,19,21)\",[C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][=Ring1][=Branch2],\"n-[4-chloro-3-([1,3]oxazolo[4,5-b]pyridin-2-yl)phenyl]butanamide\",3.37\nCc1c(Sc2ccc(Cl)cc2)c3cc(ccc3n1CC(=O)O)S(=O)(=O)C,\"InChI=1S/C18H16ClNO4S2/c1-11-18(25-13-5-3-12(19)4-6-13)15-9-14(26(2,23)24)7-8-16(15)20(11)10-17(21)22/h3-9H,10H2,1-2H3,(H,21,22)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C],2-[3-(4-chlorophenyl)sulfanyl-2-methyl-5-methylsulfonylindol-1-yl]acetic acid,0.54\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3,\"InChI=1S/C18H16ClNO4S/c1-11-3-8-16-15(9-11)18(12(2)20(16)10-17(21)22)25(23,24)14-6-4-13(19)5-7-14/h3-9H,10H2,1-2H3,(H,21,22)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"2-[3-(4-chlorophenyl)sulfonyl-2,5-dimethylindol-1-yl]acetic acid\",0.06\nCCC1(CCCCN(C)C1)c2cccc(O)c2,\"InChI=1S/C15H23NO/c1-3-15(9-4-5-10-16(2)12-15)13-7-6-8-14(17)11-13/h6-8,11,17H,3-5,9-10,12H2,1-2H3\",[C][C][C][Branch1][N][C][C][C][C][N][Branch1][C][C][C][Ring1][Branch2][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1],3-(3-ethyl-1-methylazepan-3-yl)phenol,0.8\nCOc1ccc(cc1)S(=O)(=O)NC2=CC=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C2=O)c3ccccc3,\"InChI=1S/C26H26F3N3O6S/c1-16(2)23(24(34)26(27,28)29)30-22(33)15-32-21(17-7-5-4-6-8-17)14-13-20(25(32)35)31-39(36,37)19-11-9-18(38-3)10-12-19/h4-14,16,23,31H,15H2,1-3H3,(H,30,33)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[3-[(4-methoxyphenyl)sulfonylamino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.5\nCC(C)C[C@H](CO)Nc1nc(S[C@@H](C)c2ccccc2)nc3NC(=O)Sc13,\"InChI=1S/C19H24N4O2S2/c1-11(2)9-14(10-24)20-16-15-17(23-19(25)27-15)22-18(21-16)26-12(3)13-7-5-4-6-8-13/h4-8,11-12,14,24H,9-10H2,1-3H3,(H2,20,21,22,23,25)/t12-,14+/m0/s1\",[C][C][Branch1][C][C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][=C][S][C@@H1][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1],\"7-[[(2r)-1-hydroxy-4-methylpentan-2-yl]amino]-5-[(1s)-1-phenylethyl]sulfanyl-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\",4.3\nNc1ncccc1NCc2cccc(c2)c3cccnc3,\"InChI=1S/C17H16N4/c18-17-16(7-3-9-20-17)21-11-13-4-1-5-14(10-13)15-6-2-8-19-12-15/h1-10,12,21H,11H2,(H2,18,20)\",[N][C][=N][C][=C][C][=C][Ring1][=Branch1][N][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],\"n'-[(3-pyridin-3-ylphenyl)methyl]pyridine-2,3-diamine\",3\nNc1nnc(CCSCCc2nnc(N)s2)s1,\"InChI=1S/C8H12N6S3/c9-7-13-11-5(16-7)1-3-15-4-2-6-12-14-8(10)17-6/h1-4H2,(H2,9,13)(H2,10,14)\",[N][C][=N][N][=C][Branch1][S][C][C][S][C][C][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1][S][Ring1][S],\"5-[2-[2-(5-amino-1,3,4-thiadiazol-2-yl)ethylsulfanyl]ethyl]-1,3,4-thiadiazol-2-amine\",-0.1\nCC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)N4CCN(CC4)C(=O)C)n2,\"InChI=1S/C23H29N7O/c1-16(2)30-17(3)25-15-22(30)21-9-10-24-23(27-21)26-19-5-7-20(8-6-19)29-13-11-28(12-14-29)18(4)31/h5-10,15-16H,11-14H2,1-4H3,(H,24,26,27)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=N][Ring2][Ring1][=Branch1],1-[4-[4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]piperazin-1-yl]ethanone,2.39\nCC(C)Cc1ccc(cc1)[C@@H](C)C(=O)NS(=O)(=O)C,\"InChI=1S/C14H21NO3S/c1-10(2)9-12-5-7-13(8-6-12)11(3)14(16)15-19(4,17)18/h5-8,10-11H,9H2,1-4H3,(H,15,16)/t11-/m1/s1\",[C][C][Branch1][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C],(2r)-2-[4-(2-methylpropyl)phenyl]-n-methylsulfonylpropanamide,0.51\nCOC(=O)CCCCCCC(=O)Nc1ccc2C(=O)C(=O)c3ccccc3c2c1,\"InChI=1S/C23H23NO5/c1-29-21(26)11-5-3-2-4-10-20(25)24-15-12-13-18-19(14-15)16-8-6-7-9-17(16)22(27)23(18)28/h6-9,12-14H,2-5,10-11H2,1H3,(H,24,25)\",[C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S],\"methyl 8-[(9,10-dioxophenanthren-3-yl)amino]-8-oxooctanoate\",2.6\nOc1cc(O)c2C(=O)C(=COc2c1)c3ccc(F)cc3,\"InChI=1S/C15H9FO4/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,17-18H\",[O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"3-(4-fluorophenyl)-5,7-dihydroxychromen-4-one\",3.6\nCC[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1S(=O)(=O)c3ccccc3,\"InChI=1S/C21H25ClN2O5S/c1-2-18-14-23(10-11-24(18)30(27,28)19-6-4-3-5-7-19)13-16-12-17(22)8-9-20(16)29-15-21(25)26/h3-9,12,18H,2,10-11,13-15H2,1H3,(H,25,26)/t18-/m0/s1\",[C][C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-chloro-2-[[(3s)-3-ethyl-4-phenylsulfonylpiperazin-1-yl]methyl]phenoxy]acetic acid,0.44\nC(Cc1nc2ccccc2[nH]1)c3nc4ccccc4[nH]3,\"InChI=1S/C16H14N4/c1-2-6-12-11(5-1)17-15(18-12)9-10-16-19-13-7-3-4-8-14(13)20-16/h1-8H,9-10H2,(H,17,18)(H,19,20)\",[C][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],2-[2-(1h-benzimidazol-2-yl)ethyl]-1h-benzimidazole,3.3\nCC[C@H](CO)Nc1nc(SCc2ccccc2)nc3NC(=O)Sc13,\"InChI=1S/C16H18N4O2S2/c1-2-11(8-21)17-13-12-14(20-16(22)24-12)19-15(18-13)23-9-10-6-4-3-5-7-10/h3-7,11,21H,2,8-9H2,1H3,(H2,17,18,19,20,22)/t11-/m1/s1\",[C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][C][=Ring1][=Branch1],\"7-[[(2r)-1-hydroxybutan-2-yl]amino]-5-(phenylmethylsulfanyl)-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\",3.22\nNC(=O)c1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c3ncnc(N)c13,\"InChI=1S/C12H15N5O5/c13-9-6-4(10(14)21)1-17(11(6)16-3-15-9)12-8(20)7(19)5(2-18)22-12/h1,3,5,7-8,12,18-20H,2H2,(H2,14,21)(H2,13,15,16)/t5-,7-,8-,12-/m1/s1\",[N][C][=Branch1][C][=O][C][=C][N][Branch1][S][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O][C][=N][C][=N][C][Branch1][C][N][=C][Ring2][Ring1][Ring1][Ring1][#Branch1],\"4-amino-7-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrrolo[4,5-e]pyrimidine-5-carboxamide\",-0.87\nCC(C)NCCCOc1ccc(NC(=O)C)cc1CC=C,\"InChI=1S/C17H26N2O2/c1-5-7-15-12-16(19-14(4)20)8-9-17(15)21-11-6-10-18-13(2)3/h5,8-9,12-13,18H,1,6-7,10-11H2,2-4H3,(H,19,20)\",[C][C][Branch1][C][C][N][C][C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2][C][C][=C],n-[4-[3-(propan-2-ylamino)propoxy]-3-prop-2-enylphenyl]acetamide,-0.01\nCC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)N4CCOCC4)ncc2F,\"InChI=1S/C21H25FN6O/c1-14(2)28-15(3)23-13-19(28)20-18(22)12-24-21(26-20)25-16-4-6-17(7-5-16)27-8-10-29-11-9-27/h4-7,12-14H,8-11H2,1-3H3,(H,24,25,26)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=N][C][=C][Ring2][Ring1][Ring1][F],5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)-n-(4-morpholin-4-ylphenyl)pyrimidin-2-amine,3.01\nCCOc1ccc(cc1)N2C(=Nc3ccccc3C2=O)CC,\"InChI=1S/C18H18N2O2/c1-3-17-19-16-8-6-5-7-15(16)18(21)20(17)13-9-11-14(12-10-13)22-4-2/h5-12H,3-4H2,1-2H3\",[C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][=C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][C],3-(4-ethoxyphenyl)-2-ethylquinazolin-4-one,3.27\nCCCc1c(O)c(ccc1OCCCSc2ccc(CC(=O)O)cc2Cl)C(=O)CC,\"InChI=1S/C23H27ClO5S/c1-3-6-17-20(9-8-16(23(17)28)19(25)4-2)29-11-5-12-30-21-10-7-15(13-18(21)24)14-22(26)27/h7-10,13,28H,3-6,11-12,14H2,1-2H3,(H,26,27)\",[C][C][C][C][=C][Branch1][C][O][C][=Branch2][Ring1][N][=C][C][=C][Ring1][#Branch1][O][C][C][C][S][C][=C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][Ring1][#Branch2][Cl][C][=Branch1][C][=O][C][C],2-[3-chloro-4-[3-(3-hydroxy-4-propanoyl-2-propylphenoxy)propylsulfanyl]phenyl]acetic acid,3.57\nCC1=NC(=C(NC1=O)c2ccc(CN3CCC(CC3)N4C(=O)Nc5ccccc45)cc2)c6ccccc6,\"InChI=1S/C30H29N5O2/c1-20-29(36)33-28(27(31-20)22-7-3-2-4-8-22)23-13-11-21(12-14-23)19-34-17-15-24(16-18-34)35-26-10-6-5-9-25(26)32-30(35)37/h2-14,24H,15-19H2,1H3,(H,32,37)(H,33,36)\",[C][C][=N][C][=Branch2][Ring2][S][=C][Branch1][=Branch1][N][C][Ring1][=Branch1][=O][C][=C][C][=C][Branch2][Ring1][N][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-[1-[[4-(5-methyl-6-oxo-3-phenyl-1h-pyrazin-2-yl)phenyl]methyl]piperidin-4-yl]-1h-benzimidazol-2-one,3.9\nNc1ccccc1NC(=O)c2ccc(CNc3nccc(n3)c4cccnc4)cc2,\"InChI=1S/C23H20N6O/c24-19-5-1-2-6-21(19)28-22(30)17-9-7-16(8-10-17)14-27-23-26-13-11-20(29-23)18-4-3-12-25-15-18/h1-13,15H,14,24H2,(H,28,30)(H,26,27,29)\",[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch1][C][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring2],n-(2-aminophenyl)-4-[[(4-pyridin-3-ylpyrimidin-2-yl)amino]methyl]benzamide,2.28\nC(Cc1ccccc1)NCc2ccccc2,\"InChI=1S/C15H17N/c1-3-7-14(8-4-1)11-12-16-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2\",[C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-phenyl-n-(phenylmethyl)ethanamine,1.65\nCCC1(C(=O)NC(=O)NC1=O)c2ccccc2,\"InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17)\",[C][C][C][Branch1][#C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][Branch2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-ethyl-5-phenyl-1,3-diazinane-2,4,6-trione\",0.05\nCOCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4cccnn34)cc1,\"InChI=1S/C19H19N7O3S/c1-29-12-11-23-30(27,28)15-6-4-14(5-7-15)24-19-20-10-8-16(25-19)17-13-21-18-3-2-9-22-26(17)18/h2-10,13,23H,11-12H2,1H3,(H,20,24,25)\",[C][O][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=N][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"4-[(4-imidazo[2,3-f]pyridazin-3-ylpyrimidin-2-yl)amino]-n-(2-methoxyethyl)benzenesulfonamide\",2.8\nCc1c(Sc2ccc(Cl)cc2)c3c(cccc3n1CC(=O)O)c4ccccc4,\"InChI=1S/C23H18ClNO2S/c1-15-23(28-18-12-10-17(24)11-13-18)22-19(16-6-3-2-4-7-16)8-5-9-20(22)25(15)14-21(26)27/h2-13H,14H2,1H3,(H,26,27)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][S][C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[3-(4-chlorophenyl)sulfanyl-2-methyl-4-phenylindol-1-yl]acetic acid,2.61\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccc(F)cc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C26H24F4N4O5/c1-15(2)21(22(36)26(28,29)30)33-20(35)13-34-23(17-8-10-18(27)11-9-17)31-12-19(24(34)37)32-25(38)39-14-16-6-4-3-5-7-16/h3-12,15,21H,13-14H2,1-2H3,(H,32,38)(H,33,35)\",[C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][P][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[2-(4-fluorophenyl)-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\",2.47\nOc1ccc(C(=O)Cc2ccccc2)c(O)c1,\"InChI=1S/C14H12O3/c15-11-6-7-12(14(17)9-11)13(16)8-10-4-2-1-3-5-10/h1-7,9,15,17H,8H2\",[O][C][=C][C][=C][Branch1][=C][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][=C][Ring1][S],\"1-(2,4-dihydroxyphenyl)-2-phenylethanone\",3.09\nC(N1CCN(CC1)c2nc3ccccc3s2)c4nnnn4Cc5cccs5,\"InChI=1S/C18H19N7S2/c1-2-6-16-15(5-1)19-18(27-16)24-9-7-23(8-10-24)13-17-20-21-22-25(17)12-14-4-3-11-26-14/h1-6,11H,7-10,12-13H2\",[C][Branch2][Ring1][Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=N][N][=N][N][Ring1][Branch1][C][C][=C][C][=C][S][Ring1][Branch1],\"2-[4-[[1-(thiophen-2-ylmethyl)tetrazol-5-yl]methyl]piperazin-1-yl]-1,3-benzothiazole\",3.65\nOC(=O)c1ccc2cccc(O)c2n1,\"InChI=1S/C10H7NO3/c12-8-3-1-2-6-4-5-7(10(13)14)11-9(6)8/h1-5,12H,(H,13,14)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Branch1][C][O][C][Ring1][#Branch1][=N][Ring1][O],8-hydroxyquinoline-2-carboxylic acid,3.3\nCCCC1=CC(=O)NC(=S)N1,\"InChI=1S/C7H10N2OS/c1-2-3-5-4-6(10)9-7(11)8-5/h4H,2-3H2,1H3,(H2,8,9,10,11)\",[C][C][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=S][N][Ring1][Branch2],6-propyl-2-sulfanylidene-1h-pyrimidin-4-one,0.7\nO=C1N2CCOC2=Nc3ccccc13,\"InChI=1S/C10H8N2O2/c13-9-7-3-1-2-4-8(7)11-10-12(9)5-6-14-10/h1-4H,5-6H2\",[O][=C][N][C][C][O][C][Ring1][Branch1][=N][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"2,3-dihydro-[1,3]oxazolo[2,3-b]quinazolin-5-one\",0.6\nNC(=O)c1cc(cc(c1)[N+](=O)[O-])[N+](=O)[O-],\"InChI=1S/C7H5N3O5/c8-7(11)4-1-5(9(12)13)3-6(2-4)10(14)15/h1-3H,(H2,8,11)\",[N][C][=Branch1][C][=O][C][=C][C][=Branch1][=N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][N+1][=Branch1][C][=O][O-1],\"3,5-dinitrobenzamide\n5-carbamoyl-n,n'-dihydroxybenzene-1,3-diamine oxide\n3-(dihydroxyamino)-5-(dioxidoamino)benzamide\",0.81\nNC(=O)COc1ccc(OCCNCC(O)COc2ccccc2)cc1,\"InChI=1S/C19H24N2O5/c20-19(23)14-26-18-8-6-17(7-9-18)24-11-10-21-12-15(22)13-25-16-4-2-1-3-5-16/h1-9,15,21-22H,10-14H2,(H2,20,23)\",[N][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch2][Ring1][Ring2][O][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1],2-[4-[2-[[2-hydroxy-3-(phenoxy)propyl]amino]ethoxy]phenoxy]acetamide,0.63\nCCC1(C)CC(=O)NC1=O,\"InChI=1S/C7H11NO2/c1-3-7(2)4-5(9)8-6(7)10/h3-4H2,1-2H3,(H,8,9,10)\",[C][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O],\"3-ethyl-3-methylpyrrolidine-2,5-dione\",0.23\nCCCCCC\\N=C\\1/C=CN(Cc2ccccc2)c3cc(Cl)ccc13,\"InChI=1S/C22H25ClN2/c1-2-3-4-8-14-24-21-13-15-25(17-18-9-6-5-7-10-18)22-16-19(23)11-12-20(21)22/h5-7,9-13,15-16H,2-4,8,14,17H2,1H3/b24-21+\",[C][C][C][C][C][C][\\N][=C][/C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][\\-Ring2][Ring1][C][Ring1][#Branch1],7-chloro-n-hexyl-1-(phenylmethyl)quinolin-4-imine,0.98\nCC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)O,\"InChI=1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m0/s1\",[C][C][Branch1][C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O],(2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid,-1.1\nOC(=O)CC(=O)N[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4sc(Cl)c(Cl)c4[nH]3,\"InChI=1S/C19H15Cl2N3O4S/c20-15-17-12(29-18(15)21)6-11(22-17)19(28)23-10-5-8-3-1-2-4-9(8)16(10)24-13(25)7-14(26)27/h1-4,6,10,16,22H,5,7H2,(H,23,28)(H,24,25)(H,26,27)/t10-,16-/m1/s1\",[O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][N][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][S][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Ring1][#Branch1][NH1][Ring1][#Branch2],\"3-[[(1r,2r)-2-[(2,3-dichloro4h-thieno[2,3-d]pyrrole-5-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]amino]-3-oxopropanoic acid\",1.18\nNc1nc2ccccc2s1,\"InChI=1S/C7H6N2S/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H2,8,9)\",[N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2],\"1,3-benzothiazol-2-amine\",2\nCc1ccc(F)c(Nc2ccnc(Nc3ccc(cc3)S(=O)(=O)N)n2)c1,\"InChI=1S/C17H16FN5O2S/c1-11-2-7-14(18)15(10-11)22-16-8-9-20-17(23-16)21-12-3-5-13(6-4-12)26(19,24)25/h2-10H,1H3,(H2,19,24,25)(H2,20,21,22,23)\",[C][C][=C][C][=C][Branch1][C][F][C][Branch2][Ring1][S][N][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][Ring1][P][=C][Ring2][Ring1][=Branch2],4-[[4-[(2-fluoro-5-methylphenyl)amino]pyrimidin-2-yl]amino]benzenesulfonamide,3.1\nCCOCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)O,\"InChI=1S/C17H22N4O2/c1-4-23-9-13-20-14-15(21(13)10-17(2,3)22)11-7-5-6-8-12(11)19-16(14)18/h5-8,22H,4,9-10H2,1-3H3,(H2,18,19)\",[C][C][O][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][Branch1][C][C][O],\"1-[4-amino-2-(ethoxymethyl)imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol\",1.69\nFC(F)(F)c1nnc2ccc(nn12)n3ccnc3,\"InChI=1S/C9H5F3N6/c10-9(11,12)8-15-14-6-1-2-7(16-18(6)8)17-4-3-13-5-17/h1-5H\",[F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1],\"6-imidazol-1-yl-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\",0.91\nCc1cc(C)c(C(=O)N[C@@H](Cc2ccc(OCCCNc3ccccn3)cc2)C(=O)O)c(C)c1,\"InChI=1S/C27H31N3O4/c1-18-15-19(2)25(20(3)16-18)26(31)30-23(27(32)33)17-21-8-10-22(11-9-21)34-14-6-13-29-24-7-4-5-12-28-24/h4-5,7-12,15-16,23H,6,13-14,17H2,1-3H3,(H,28,29)(H,30,31)(H,32,33)/t23-/m0/s1\",[C][C][=C][C][Branch1][C][C][=C][Branch2][Ring2][#Branch1][C][=Branch1][C][=O][N][C@@H1][Branch2][Ring1][=Branch2][C][C][=C][C][=C][Branch1][=C][O][C][C][C][N][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring1][P][C][=Branch1][C][=O][O][C][Branch1][C][C][=C][Ring2][Ring1][P],\"(2s)-3-[4-[3-(pyridin-2-ylamino)propoxy]phenyl]-2-[(2,4,6-trimethylbenzoyl)amino]propanoic acid\",0.49\nCOc1cc2ncc(C(=O)N)c(Nc3ccc(F)c(Cl)c3)c2cc1OC,\"InChI=1S/C18H15ClFN3O3/c1-25-15-6-10-14(7-16(15)26-2)22-8-11(18(21)24)17(10)23-9-3-4-13(20)12(19)5-9/h3-8H,1-2H3,(H2,21,24)(H,22,23)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C],\"4-[(3-chloro-4-fluorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",3.22\nOC(=O)c1cc(nc2ccccc12)c3ccccc3,\"InChI=1S/C16H11NO2/c18-16(19)13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10H,(H,18,19)\",[O][C][=Branch1][C][=O][C][=C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-phenylquinoline-4-carboxylic acid,-0.7\nOC(=O)c1ccccc1c2ccc(Cl)c(c2)C(=O)NCC3(O)CCCCCC3,\"InChI=1S/C22H24ClNO4/c23-19-10-9-15(16-7-3-4-8-17(16)21(26)27)13-18(19)20(25)24-14-22(28)11-5-1-2-6-12-22/h3-4,7-10,13,28H,1-2,5-6,11-12,14H2,(H,24,25)(H,26,27)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][O][C][C][C][C][C][C][Ring1][Branch2],2-[4-chloro-3-[(1-hydroxycycloheptyl)methylcarbamoyl]phenyl]benzoic acid,-0.34\nNC(Cc1ccc(cc1)N(CCCl)CCCl)C(=O)O,\"InChI=1S/C13H18Cl2N2O2/c14-5-7-17(8-6-15)11-3-1-10(2-4-11)9-12(16)13(18)19/h1-4,12H,5-9,16H2,(H,18,19)\",[N][C][Branch2][Ring1][Branch1][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][Ring2][C][C][Cl][C][C][Cl][C][=Branch1][C][=O][O],2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid,0.39\nClc1ccc(COC(Cn2ccnc2)c3ccc(Cl)cc3Cl)cc1,\"InChI=1S/C18H15Cl3N2O/c19-14-3-1-13(2-4-14)11-24-18(10-23-8-7-22-12-23)16-6-5-15(20)9-17(16)21/h1-9,12,18H,10-11H2\",[Cl][C][=C][C][=C][Branch2][Ring1][#Branch2][C][O][C][Branch1][=Branch2][C][N][C][=C][N][=C][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][C][=C][Ring2][Ring1][#Branch1],\"1-[2-[(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl]imidazole\",2.54\nNc1ncnc2[nH]ccc12,\"InChI=1S/C6H6N4/c7-5-4-1-2-8-6(4)10-3-9-5/h1-3H,(H3,7,8,9,10)\",[N][C][=N][C][=N][C][NH1][C][=C][C][Ring1][=Branch2][=Ring1][Branch1],\"7h-pyrrolo[3,2-e]pyrimidin-4-amine\",1.78\nClc1ccc2[nH]ncc2c1,\"InChI=1S/C7H5ClN2/c8-6-1-2-7-5(3-6)4-9-10-7/h1-4H,(H,9,10)\",[Cl][C][=C][C][=C][NH1][N][=C][C][Ring1][Branch1][=C][Ring1][=Branch2],5-chloro-1h-indazole,2.44\nCN1CCN(CC1)C(=O)c2cc3ccccc3[nH]2,\"InChI=1S/C14H17N3O/c1-16-6-8-17(9-7-16)14(18)13-10-11-4-2-3-5-12(11)15-13/h2-5,10,15H,6-9H2,1H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],1h-indol-2-yl-(4-methylpiperazin-1-yl)methanone,1.7\nNC(=O)C[S+]([O-])C(c1ccccc1)c2ccccc2,\"InChI=1S/C15H15NO2S/c16-14(17)11-19(18)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15H,11H2,(H2,16,17)\",[N][C][=Branch1][C][=O][C][S+1][Branch1][C][O-1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[di(phenyl)methylsulfinyl]acetamide,1.12\nNC(=N)N1CCc2ccccc2C1,\"InChI=1S/C10H13N3/c11-10(12)13-6-5-8-3-1-2-4-9(8)7-13/h1-4H,5-7H2,(H3,11,12)\",[N][C][=Branch1][C][=N][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2],\"3,4-dihydro-1h-isoquinoline-2-carboximidamide\",-1.01\nNC(=O)c1c(NC(=O)NCCCCN2CCCC2)snc1OCc3c(F)cc(Br)cc3F,\"InChI=1S/C20H24BrF2N5O3S/c21-12-9-14(22)13(15(23)10-12)11-31-18-16(17(24)29)19(32-27-18)26-20(30)25-5-1-2-6-28-7-3-4-8-28/h9-10H,1-8,11H2,(H2,24,29)(H2,25,26,30)\",[N][C][=Branch1][C][=O][C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][N][C][C][C][C][N][C][C][C][C][Ring1][Branch1][S][N][=C][Ring2][Ring1][C][O][C][C][=C][Branch1][C][F][C][=C][Branch1][C][Br][C][=C][Ring1][Branch2][F],\"3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-(4-pyrrolidin-1-ylbutylcarbamoylamino)-1,2-thiazole-4-carboxamide\",2.5\nCN(c1ccc2c(C)n(C)nc2c1)c3ccnc(Nc4ccc(C)c(c4)S(=O)(=O)N)n3,\"InChI=1S/C21H23N7O2S/c1-13-5-6-15(11-19(13)31(22,29)30)24-21-23-10-9-20(25-21)27(3)16-7-8-17-14(2)28(4)26-18(17)12-16/h5-12H,1-4H3,(H2,22,29,30)(H,23,24,25)\",[C][N][Branch2][Ring1][Ring2][C][C][=C][C][=C][Branch1][C][C][N][Branch1][C][C][N][=C][Ring1][#Branch1][C][=Ring1][O][C][=C][C][=N][C][Branch2][Ring1][#Branch1][N][C][=C][C][=C][Branch1][C][C][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][Ring2][Ring1][C],\"5-[[4-[(2,3-dimethylindazol-6-yl)-methylamino]pyrimidin-2-yl]amino]-2-methylbenzenesulfonamide\",3.3\nCc1ccc2nc(NCCN)c3ncc(C)n3c2c1,\"InChI=1S/C14H17N5/c1-9-3-4-11-12(7-9)19-10(2)8-17-14(19)13(18-11)16-6-5-15/h3-4,7-8H,5-6,15H2,1-2H3,(H,16,18)\",[C][C][=C][C][=C][N][=C][Branch1][Branch1][N][C][C][N][C][=N][C][=C][Branch1][C][C][N][Ring1][=Branch1][C][Ring1][=C][=C][Ring2][Ring1][C],\"n-(1,8-dimethylimidazo[2,1-c]quinoxalin-4-yl)ethane-1,2-diamine\",0.88\nCNC(=O)c1ccc(C)c(c1)N2C(=CC(=C(Br)C2=O)OCc3ccc(F)cc3F)C,\"InChI=1S/C22H19BrF2N2O3/c1-12-4-5-14(21(28)26-3)9-18(12)27-13(2)8-19(20(23)22(27)29)30-11-15-6-7-16(24)10-17(15)25/h4-10H,11H2,1-3H3,(H,26,28)\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=Branch1][Ring2][=C][Ring1][#Branch1][N][C][=Branch2][Ring1][O][=C][C][=Branch1][=Branch2][=C][Branch1][C][Br][C][Ring1][#Branch1][=O][O][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C],\"3-[3-bromo-4-[(2,4-difluorophenyl)methoxy]-6-methyl-2-oxopyridin-1-yl]-n,4-dimethylbenzamide\",2.8\nOc1ccc(Cl)cc1C(=O)Nc2ccccc2,\"InChI=1S/C13H10ClNO2/c14-9-6-7-12(16)11(8-9)13(17)15-10-4-2-1-3-5-10/h1-8,16H,(H,15,17)\",[O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],5-chloro-2-hydroxy-n-phenylbenzamide,2.9\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccccc34)c2C(=O)N5C[C@@H](O)[C@@H](O)C5,\"InChI=1S/C26H28N4O5S/c1-14(2)11-30-25-22(23(33)28(3)26(30)35)21(24(34)29-12-18(31)19(32)13-29)20(36-25)10-15-8-9-27-17-7-5-4-6-16(15)17/h4-9,14,18-19,31-32H,10-13H2,1-3H3/t18-,19+\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][C][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C@@H1][Branch1][C][O][C@@H1][Branch1][C][O][C][Ring1][#Branch1],\"5-[(3s,4r)-3,4-dihydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)-6-(quinolin-4-ylmethyl)thieno[3,2-e]pyrimidine-2,4-dione\",1.18\nO=C1N([Se]c2ccccc12)c3ccccc3,InChI=1S/C13H9NOSe/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H,[O][=C][N][Branch1][N][Se][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-phenyl-1,2-benzoselenazol-3-one\",3.31\nCOc1ccc2C=CC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1,\"InChI=1S/C25H30N4O4/c1-31-21-4-2-18-3-5-25(30)29(22(18)15-21)11-10-28-8-6-19(7-9-28)26-16-20-14-23-24(17-27-20)33-13-12-32-23/h2-5,14-15,17,19,26H,6-13,16H2,1H3\",[C][O][C][=C][C][=C][C][=C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C],\"1-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-7-methoxyquinolin-2-one\",1.31\nCC(C)COc1cc(OC(C)C)cc(c1)C(=O)Nc2ccc(cn2)C(=O)O,\"InChI=1S/C20H24N2O5/c1-12(2)11-26-16-7-15(8-17(9-16)27-13(3)4)19(23)22-18-6-5-14(10-21-18)20(24)25/h5-10,12-13H,11H2,1-4H3,(H,24,25)(H,21,22,23)\",[C][C][Branch1][C][C][C][O][C][=C][C][Branch1][#Branch1][O][C][Branch1][C][C][C][=C][C][=Branch1][Ring2][=C][Ring1][#Branch2][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O],6-[[3-(2-methylpropoxy)-5-propan-2-yloxybenzoyl]amino]pyridine-3-carboxylic acid,1.6\nClc1ccc2NC(=O)CN(C(c3ccccc3)c2c1)C(=O)c4ccccc4,\"InChI=1S/C22H17ClN2O2/c23-17-11-12-19-18(13-17)21(15-7-3-1-4-8-15)25(14-20(26)24-19)22(27)16-9-5-2-6-10-16/h1-13,21H,14H2,(H,24,26)\",[Cl][C][=C][C][=C][N][C][=Branch1][C][=O][C][N][Branch2][Ring1][Ring1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=C][=C][Ring2][Ring1][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4-(benzoyl)-7-chloro-5-phenyl-3,5-dihydro-1h-1,4-benzodiazepin-2-one\",3.31\nCC(C)C[C@H](NC(=O)N1CCOCC1)C(=O)N[C@@H](CCc2ccccc2)\\C=C\\S(=O)(=O)c3ccccc3,\"InChI=1S/C28H37N3O5S/c1-22(2)21-26(30-28(33)31-16-18-36-19-17-31)27(32)29-24(14-13-23-9-5-3-6-10-23)15-20-37(34,35)25-11-7-4-8-12-25/h3-12,15,20,22,24,26H,13-14,16-19,21H2,1-2H3,(H,29,32)(H,30,33)/b20-15+/t24-,26-/m0/s1\",[C][C][Branch1][C][C][C][C@H1][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@@H1][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][\\C][=C][\\S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-[(2s)-4-methyl-1-oxo-1-[[(e,3s)-5-phenyl-1-phenylsulfonylpent-1-en-3-yl]amino]pentan-2-yl]morpholine-4-carboxamide\",3.4\nCCC(=O)O[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C,\"InChI=1S/C22H32O3/c1-4-20(24)25-19-8-7-17-16-6-5-14-13-15(23)9-11-21(14,2)18(16)10-12-22(17,19)3/h13,16-19H,4-12H2,1-3H3/t16-,17-,18-,19-,21-,22-/m0/s1\",[C][C][C][=Branch1][C][=O][O][C@H1][C][C][C@H1][C@@H1][C][C][C][=C][C][=Branch1][C][=O][C][C][C@][Ring1][#Branch1][Branch1][C][C][C@H1][Ring1][N][C][C][C@][Ring2][Ring1][Ring1][Ring1][S][C],\"[(8r,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] propanoate\",3.3\nCCCC(C)(COC(=O)N)COC(=O)NC(C)C,\"InChI=1S/C12H24N2O4/c1-5-6-12(4,7-17-10(13)15)8-18-11(16)14-9(2)3/h9H,5-8H2,1-4H3,(H2,13,15)(H,14,16)\",[C][C][C][C][Branch1][C][C][Branch1][Branch2][C][O][C][=Branch1][C][=O][N][C][O][C][=Branch1][C][=O][N][C][Branch1][C][C][C],[2-(carbamoyloxymethyl)-2-methylpentyl] n-propan-2-ylcarbamate,2.01\nCC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN2CCC3(CC2)Cc4cc(Cl)ccc4O3,\"InChI=1S/C23H27ClN2O5/c1-15(27)25-20-4-3-18(28)11-22(20)30-14-19(29)13-26-8-6-23(7-9-26)12-16-10-17(24)2-5-21(16)31-23/h2-5,10-11,19,28-29H,6-9,12-14H2,1H3,(H,25,27)/t19-/m0/s1\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][C@@H1][Branch1][C][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][Ring1][N],\"n-[2-[(2s)-3-(5-chlorospiro[3h-1-benzofuran-2,4'-piperidine]-1'-yl)-2-hydroxypropoxy]-4-hydroxyphenyl]acetamide\",2.76\n[O-][N+](=O)c1ccc2[nH]ncc2c1,\"InChI=1S/C7H5N3O2/c11-10(12)6-1-2-7-5(3-6)4-8-9-7/h1-4H,(H,8,9)\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][NH1][N][=C][C][Ring1][Branch1][=C][Ring1][=Branch2],5-nitro-1h-indazole,2.2\nCc1cc(C)cc(c1)c2[nH]c3ccccc3c2CCNCCCCc4ccncc4,\"InChI=1S/C27H31N3/c1-20-17-21(2)19-23(18-20)27-25(24-8-3-4-9-26(24)30-27)12-16-28-13-6-5-7-22-10-14-29-15-11-22/h3-4,8-11,14-15,17-19,28,30H,5-7,12-13,16H2,1-2H3\",[C][C][=C][C][Branch1][C][C][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][N][C][C][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1],\"n-[2-[2-(3,5-dimethylphenyl)-1h-indol-3-yl]ethyl]-4-pyridin-4-ylbutan-1-amine\",3.3\nCOC(CN1C(=O)NC2=C(C=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C2=O)c3ccccc3)C1=O)OC,\"InChI=1S/C25H27F3N4O7/c1-13(2)19(21(34)25(26,27)28)29-17(33)11-31-16(14-8-6-5-7-9-14)10-15-20(23(31)36)30-24(37)32(22(15)35)12-18(38-3)39-4/h5-10,13,18-19H,11-12H2,1-4H3,(H,29,33)(H,30,37)\",[C][O][C][Branch2][=Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][Branch2][Ring2][P][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][S][=O][O][C],\"2-[3-(2,2-dimethoxyethyl)-2,4,8-trioxo-6-phenyl-1h-pyrido[3,4-d]pyrimidin-7-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.56\nCCOC(=O)Nc1ccc2Sc3ccccc3N(C(=O)CCN4CCOCC4)c2c1,\"InChI=1S/C22H25N3O4S/c1-2-29-22(27)23-16-7-8-20-18(15-16)25(17-5-3-4-6-19(17)30-20)21(26)9-10-24-11-13-28-14-12-24/h3-8,15H,2,9-14H2,1H3,(H,23,27)\",[C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][#C][C][=Branch1][C][=O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2],ethyl n-[10-(3-morpholin-4-ylpropanoyl)phenothiazin-2-yl]carbamate,3.1\nCc1ccc(C)c(OCCCC(C)(C)C(=O)O)c1,\"InChI=1S/C15H22O3/c1-11-6-7-12(2)13(10-11)18-9-5-8-15(3,4)14(16)17/h6-7,10H,5,8-9H2,1-4H3,(H,16,17)\",[C][C][=C][C][=C][Branch1][C][C][C][Branch1][P][O][C][C][C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][=C][Ring1][P],\"5-(2,5-dimethylphenoxy)-2,2-dimethylpentanoic acid\",0.72\nO=S(=O)(Nc1cccnc1)c2ccccc2,\"InChI=1S/C11H10N2O2S/c14-16(15,11-6-2-1-3-7-11)13-10-5-4-8-12-9-10/h1-9,13H\",[O][=S][=Branch1][C][=O][Branch1][#Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-pyridin-3-ylbenzenesulfonamide,0.84\nCOCCOc1cc2nccc(Nc3cc(O)c(Cl)cc3F)c2cc1OC,\"InChI=1S/C19H18ClFN2O4/c1-25-5-6-27-19-10-15-11(7-18(19)26-2)14(3-4-22-15)23-16-9-17(24)12(20)8-13(16)21/h3-4,7-10,24H,5-6H2,1-2H3,(H,22,23)\",[C][O][C][C][O][C][=C][C][=N][C][=C][C][Branch1][P][N][C][=C][C][Branch1][C][O][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][F][=C][Ring1][S][C][=C][Ring2][Ring1][Ring2][O][C],2-chloro-4-fluoro-5-[[6-methoxy-7-(2-methoxyethoxy)quinolin-4-yl]amino]phenol,2.64\nCc1ccc(cc1)n2nc(cc2NC(=O)Nc3ccc(OCCN4CCOCC4)c5ccccc35)C(C)(C)C,\"InChI=1S/C31H37N5O3/c1-22-9-11-23(12-10-22)36-29(21-28(34-36)31(2,3)4)33-30(37)32-26-13-14-27(25-8-6-5-7-24(25)26)39-20-17-35-15-18-38-19-16-35/h5-14,21H,15-20H2,1-4H3,(H2,32,33,37)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][N][=C][Branch2][Ring2][#Branch1][C][=C][Ring1][Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][N][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C],1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[4-(2-morpholin-4-ylethoxy)naphthalen-1-yl]urea,4.49\nO=C1C2=Nc3ccccc3CN2c4ccccc14,\"InChI=1S/C15H10N2O/c18-14-11-6-2-4-8-13(11)17-9-10-5-1-3-7-12(10)16-15(14)17/h1-8H,9H2\",[O][=C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1],\"12h-indolo[2,1-b]quinazolin-6-one\",2.71\nCCNC1=CC=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccccc2,\"InChI=1S/C21H24F3N3O3/c1-4-25-15-10-11-16(14-8-6-5-7-9-14)27(20(15)30)12-17(28)26-18(13(2)3)19(29)21(22,23)24/h5-11,13,18,25H,4,12H2,1-3H3,(H,26,28)\",[C][C][N][C][=C][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-(3-ethylamino-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.37\nCc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(F)c(F)c4,\"InChI=1S/C24H29F2N3O4S/c1-17-2-5-21(6-3-17)34(31,32)27-24(30)29-12-8-18(9-13-29)28-14-10-19(11-15-28)33-20-4-7-22(25)23(26)16-20/h2-7,16,18-19H,8-15H2,1H3,(H,27,30)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2],\"4-[4-(3,4-difluorophenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\",0.75\nCOc1ccc(Cl)cc1NC(=O)Nc2cnccn2,\"InChI=1S/C12H11ClN4O2/c1-19-10-3-2-8(13)6-9(10)16-12(18)17-11-7-14-4-5-15-11/h2-7H,1H3,(H2,15,16,17,18)\",[C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][N][C][=C][N][=C][C][=N][Ring1][=Branch1],1-(5-chloro-2-methoxyphenyl)-3-pyrazin-2-ylurea,3.63\nNCc1ccc(NC(=O)c2cc(Nc3ncccn3)c4cc(ccc4c2)\\C(=N\\O)\\N)cc1,\"InChI=1S/C23H21N7O2/c24-13-14-2-6-18(7-3-14)28-22(31)17-10-15-4-5-16(21(25)30-32)11-19(15)20(12-17)29-23-26-8-1-9-27-23/h1-12,32H,13,24H2,(H2,25,30)(H,28,31)(H,26,27,29)\",[N][C][C][=C][C][=C][Branch2][Ring2][#Branch1][N][C][=Branch1][C][=O][C][=C][C][Branch1][#Branch2][N][C][=N][C][=C][C][=N][Ring1][=Branch1][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][P][\\C][=Branch1][Ring1][=N][\\O][\\N][C][=C][Ring2][Ring1][=C],n-[4-(aminomethyl)phenyl]-6-(n'-hydroxycarbamimidoyl)-4-(pyrimidin-2-ylamino)naphthalene-2-carboxamide,-0.85\nOC1CCN(CC1)C(=O)[C@H](Cc2ccccc2)NC(=O)c3cc4cc(Cl)ccc4[nH]3,\"InChI=1S/C23H24ClN3O3/c24-17-6-7-19-16(13-17)14-20(25-19)22(29)26-21(12-15-4-2-1-3-5-15)23(30)27-10-8-18(28)9-11-27/h1-7,13-14,18,21,25,28H,8-12H2,(H,26,29)/t21-/m0/s1\",[O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],5-chloro-n-[(2s)-1-(4-hydroxypiperidin-1-yl)-1-oxo-3-phenylpropan-2-yl]-1h-indole-2-carboxamide,3.6\nCCN(C1CCN(CCC(C2CCN(CC2)S(=O)(=O)CC)c3ccccc3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H47N3O5S2/c1-4-35(32(36)25-26-11-13-30(14-12-26)41(3,37)38)29-17-20-33(21-18-29)22-19-31(27-9-7-6-8-10-27)28-15-23-34(24-16-28)42(39,40)5-2/h6-14,28-29,31H,4-5,15-25H2,1-3H3\",[C][C][N][Branch2][Ring2][=C][C][C][C][N][Branch2][Ring2][C][C][C][C][Branch2][Ring1][Ring2][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-ethyl-n-[1-[3-(1-ethylsulfonylpiperidin-4-yl)-3-phenylpropyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)acetamide,1.63\nCOc1cccc2sc(NC(=O)c3ccccc3)nc12,\"InChI=1S/C15H12N2O2S/c1-19-11-8-5-9-12-13(11)16-15(20-12)17-14(18)10-6-3-2-4-7-10/h2-9H,1H3,(H,16,17,18)\",[C][O][C][=C][C][=C][C][S][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][Ring2][Ring1][C][=Ring1][=C],\"n-(4-methoxy-1,3-benzothiazol-2-yl)benzamide\",3.96\nCOc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1,\"InChI=1S/C24H30N4O5/c1-30-19-2-3-21-20(13-19)28(24(29)16-33-21)9-8-27-6-4-17(5-7-27)25-14-18-12-22-23(15-26-18)32-11-10-31-22/h2-3,12-13,15,17,25H,4-11,14,16H2,1H3\",[C][O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C],\"4-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-6-methoxy-1,4-benzoxazin-3-one\",1.24\nCOc1ccc(\\C=C/2\\CCc3ccccc3C2=O)cc1CN4CCOCC4,\"InChI=1S/C23H25NO3/c1-26-22-9-6-17(15-20(22)16-24-10-12-27-13-11-24)14-19-8-7-18-4-2-3-5-21(18)23(19)25/h2-6,9,14-15H,7-8,10-13,16H2,1H3/b19-14-\",[C][O][C][=C][C][=C][Branch1][P][\\C][=C][\\C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][/-Ring1][#Branch2][=O][C][=C][Ring2][Ring1][C][C][N][C][C][O][C][C][Ring1][=Branch1],\"(2z)-2-[[4-methoxy-3-(morpholin-4-ylmethyl)phenyl]methylidene]-3,4-dihydronaphthalen-1-one\",3.8\nCC(C)(C)c1ccc(cc1)C(O)CCCN2CCC(CC2)C(O)(c3ccccc3)c4ccccc4,\"InChI=1S/C32H41NO2/c1-31(2,3)26-18-16-25(17-19-26)30(34)15-10-22-33-23-20-29(21-24-33)32(35,27-11-6-4-7-12-27)28-13-8-5-9-14-28/h4-9,11-14,16-19,29-30,34-35H,10,15,20-24H2,1-3H3\",[C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],1-(4-tert-butylphenyl)-4-[4-[hydroxy-di(phenyl)methyl]piperidin-1-yl]butan-1-ol,3.99\nNC(=O)c1cnc(N[C@H]2CCCNC2)c3cc(sc13)c4ccc(F)c(F)c4,\"InChI=1S/C19H18F2N4OS/c20-14-4-3-10(6-15(14)21)16-7-12-17(27-16)13(18(22)26)9-24-19(12)25-11-2-1-5-23-8-11/h3-4,6-7,9,11,23H,1-2,5,8H2,(H2,22,26)(H,24,25)/t11-/m0/s1\",[N][C][=Branch1][C][=O][C][=C][N][=C][Branch1][#Branch2][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][C][=C][Branch1][#Branch1][S][C][Ring1][S][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2],\"2-(3,4-difluorophenyl)-4-[[(3s)-piperidin-3-yl]amino]thieno[2,3-d]pyridine-7-carboxamide\",2.17\nO[C@@H](CNCCCOCCOCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H28N2O5S/c25-18-8-7-17(21-20(18)24-22(27)30-21)19(26)15-23-10-4-11-28-13-14-29-12-9-16-5-2-1-3-6-16/h1-3,5-8,19,23,25-26H,4,9-15H2,(H,24,27)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][C][O][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-phenylethoxy)ethoxy]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\",1.09\nCOc1cc(cc(OC)c1OC)C(=O)Nc2ccc(Cl)c(c2)c3nc4ccccc4[nH]3,\"InChI=1S/C23H20ClN3O4/c1-29-19-10-13(11-20(30-2)21(19)31-3)23(28)25-14-8-9-16(24)15(12-14)22-26-17-6-4-5-7-18(17)27-22/h4-12H,1-3H3,(H,25,28)(H,26,27)\",[C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],\"n-[3-(1h-benzimidazol-2-yl)-4-chlorophenyl]-3,4,5-trimethoxybenzamide\",3.83\nCCNC1=Nc2ccccc2C(=NC1c3cccs3)c4ccccc4,\"InChI=1S/C21H19N3S/c1-2-22-21-20(18-13-8-14-25-18)24-19(15-9-4-3-5-10-15)16-11-6-7-12-17(16)23-21/h3-14,20H,2H2,1H3,(H,22,23)\",[C][C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][N][=N][C][Ring1][O][C][=C][C][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-ethyl-5-phenyl-3-thiophen-2-yl-3h-1,4-benzodiazepin-2-amine\",3.98\nCc1nc(nc(N2CCCC2)c1Cl)c3ccccn3,\"InChI=1S/C14H15ClN4/c1-10-12(15)14(19-8-4-5-9-19)18-13(17-10)11-6-2-3-7-16-11/h2-3,6-7H,4-5,8-9H2,1H3\",[C][C][=N][C][=Branch1][S][=N][C][Branch1][Branch2][N][C][C][C][C][Ring1][Branch1][=C][Ring1][O][Cl][C][=C][C][=C][C][=N][Ring1][=Branch1],5-chloro-4-methyl-2-pyridin-2-yl-6-pyrrolidin-1-ylpyrimidine,3.2\nC[C@@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)C[C@H](C)N1C(=O)Cc3ccccc3,\"InChI=1S/C23H27ClN2O4/c1-16-12-25(14-19-11-20(24)8-9-21(19)30-15-23(28)29)13-17(2)26(16)22(27)10-18-6-4-3-5-7-18/h3-9,11,16-17H,10,12-15H2,1-2H3,(H,28,29)/t16-,17+\",[C][C@@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C@H1][Branch1][C][C][N][Ring2][Ring1][Ring2][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[4-chloro-2-[[(3r,5s)-3,5-dimethyl-4-(2-phenylacetyl)piperazin-1-yl]methyl]phenoxy]acetic acid\",0.7\n[O-][S+](CCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3)c4ccccc4,\"InChI=1S/C23H20N2O3S/c26-22-21(16-17-29(28)20-14-8-3-9-15-20)23(27)25(19-12-6-2-7-13-19)24(22)18-10-4-1-5-11-18/h1-15,21H,16-17H2\",[O-1][S+1][Branch2][Ring2][C][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1,2-di(phenyl)-4-(2-phenylsulfinylethyl)pyrazolidine-3,5-dione\",-0.51\nCOc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC,\"InChI=1S/C20H21NO4/c1-22-17-6-5-13(10-18(17)23-2)9-16-15-12-20(25-4)19(24-3)11-14(15)7-8-21-16/h5-8,10-12H,9H2,1-4H3\",[C][O][C][=C][C][=C][Branch2][Ring1][Branch2][C][C][=N][C][=C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][=C][Ring1][#Branch2][C][=C][Ring2][Ring1][Branch1][O][C],\"1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxyisoquinoline\",2.81\nClc1ccc(CN(Cc2ccc(Cl)cc2)c3nn[nH]n3)cc1,\"InChI=1S/C15H13Cl2N5/c16-13-5-1-11(2-6-13)9-22(15-18-20-21-19-15)10-12-3-7-14(17)8-4-12/h1-8H,9-10H2,(H,18,19,20,21)\",[Cl][C][=C][C][=C][Branch2][Ring1][Branch2][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][N][=N][NH1][N][=Ring1][Branch1][C][=C][Ring2][Ring1][Branch1],\"n,n-bis[(4-chlorophenyl)methyl]-2h-tetrazol-5-amine\",2.74\nCc1c(F)ccc2c1c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O,\"InChI=1S/C18H15ClFNO2S/c1-10-14(20)7-8-15-17(10)18(11(2)21(15)9-16(22)23)24-13-5-3-12(19)4-6-13/h3-8H,9H2,1-2H3,(H,22,23)\",[C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O],\"2-[3-(4-chlorophenyl)sulfanyl-5-fluoro-2,4-dimethylindol-1-yl]acetic acid\",2.23\nNc1n[nH]c(N)c1Cc2ccc3OCOc3c2,\"InChI=1S/C11H12N4O2/c12-10-7(11(13)15-14-10)3-6-1-2-8-9(4-6)17-5-16-8/h1-2,4H,3,5H2,(H5,12,13,14,15)\",[N][C][=N][NH1][C][Branch1][C][N][=C][Ring1][=Branch1][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2],\"4-(1,3-benzodioxol-5-ylmethyl)-1h-pyrazole-3,5-diamine\",0.47\nCOc1ccc(cc1CNCCO)c2ccc3c(nc(nc3n2)N4C[C@@H](C)O[C@@H](C)C4)N5CCOCC5,\"InChI=1S/C27H36N6O4/c1-18-16-33(17-19(2)37-18)27-30-25-22(26(31-27)32-9-12-36-13-10-32)5-6-23(29-25)20-4-7-24(35-3)21(14-20)15-28-8-11-34/h4-7,14,18-19,28,34H,8-13,15-17H2,1-3H3/t18-,19+\",[C][O][C][=C][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][C][N][C][C][O][C][=C][C][=C][C][=Branch2][Ring1][#Branch2][=N][C][=Branch1][Branch2][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2][N][C][C@@H1][Branch1][C][C][O][C@@H1][Branch1][C][C][C][Ring1][Branch2][N][C][C][O][C][C][Ring1][=Branch1],\"2-[[5-[2-[(2r,6s)-2,6-dimethylmorpholin-4-yl]-4-morpholin-4-ylpyrido[5,6-e]pyrimidin-7-yl]-2-methoxyphenyl]methylamino]ethanol\",1.31\nOC(=O)c1cc2ccccc2n1Cc3ccccc3,\"InChI=1S/C16H13NO2/c18-16(19)15-10-13-8-4-5-9-14(13)17(15)11-12-6-2-1-3-7-12/h1-10H,11H2,(H,18,19)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1],1-(phenylmethyl)indole-2-carboxylic acid,0.78\nNc1ccc2C(=O)C(=O)c3ccccc3c2c1,\"InChI=1S/C14H9NO2/c15-8-5-6-11-12(7-8)9-3-1-2-4-10(9)13(16)14(11)17/h1-7H,15H2\",[N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S],\"3-aminophenanthrene-9,10-dione\",2.39\nClc1ccc(NC(=O)N2CCN(C[C@@H]3CCCN(Cc4ccccc4)C3)CC2)cc1Cl,\"InChI=1S/C24H30Cl2N4O/c25-22-9-8-21(15-23(22)26)27-24(31)30-13-11-28(12-14-30)17-20-7-4-10-29(18-20)16-19-5-2-1-3-6-19/h1-3,5-6,8-9,15,20H,4,7,10-14,16-18H2,(H,27,31)/t20-/m0/s1\",[Cl][C][=C][C][=C][Branch2][Ring2][=Branch1][N][C][=Branch1][C][=O][N][C][C][N][Branch2][Ring1][Branch1][C][C@@H1][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=N][C][C][Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][=N][Cl],\"n-(3,4-dichlorophenyl)-4-[[(3r)-1-(phenylmethyl)piperidin-3-yl]methyl]piperazine-1-carboxamide\",4.26\nCC(=O)Nc1nc(ns1)c2ccccc2,\"InChI=1S/C10H9N3OS/c1-7(14)11-10-12-9(13-15-10)8-5-3-2-4-6-8/h2-6H,1H3,(H,11,12,13,14)\",[C][C][=Branch1][C][=O][N][C][=N][C][=Branch1][Branch1][=N][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-(3-phenyl-1,2,4-thiadiazol-5-yl)acetamide\",2.8\nOC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc(cc1)[N+](=O)[O-],\"InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)/t8-,9-/m1/s1\",[O][C][C@@H1][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1],\"2,2-dichloro-n-[(1r,2r)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide\",1.15\nO[C@@H](CNCCSCCCNCCc1cccc(Cl)c1Cl)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H27Cl2N3O3S2/c23-16-4-1-3-14(19(16)24)7-9-25-8-2-11-31-12-10-26-13-18(29)15-5-6-17(28)20-21(15)32-22(30)27-20/h1,3-6,18,25-26,28-29H,2,7-13H2,(H,27,30)/t18-/m0/s1\",[O][C@@H1][Branch2][Ring1][Branch2][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"7-[(1r)-2-[2-[3-[2-(2,3-dichlorophenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",2.2\nC[C@@](Cc1ccc(O)c(O)c1)(NN)C(=O)O,\"InChI=1S/C10H14N2O4/c1-10(12-11,9(15)16)5-6-2-3-7(13)8(14)4-6/h2-4,12-14H,5,11H2,1H3,(H,15,16)/t10-/m0/s1\",[C][C@@][Branch1][S][C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2][Branch1][Ring1][N][N][C][=Branch1][C][=O][O],\"(2s)-3-(3,4-dihydroxyphenyl)-2-hydrazinyl-2-methylpropanoic acid\",-0.7\nCC(=O)Nc1cccc2c1c(Oc3ccc(Cl)cc3)c(C)n2CC(=O)O,\"InChI=1S/C19H17ClN2O4/c1-11-19(26-14-8-6-13(20)7-9-14)18-15(21-12(2)23)4-3-5-16(18)22(11)10-17(24)25/h3-9H,10H2,1-2H3,(H,21,23)(H,24,25)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O],2-[4-acetamido-3-(4-chlorophenoxy)-2-methylindol-1-yl]acetic acid,-1.41\nCC1=C(CCN2CCC(CC2)c3noc4cc(F)ccc34)C(=O)N5CCCCC5=N1,\"InChI=1S/C23H27FN4O2/c1-15-18(23(29)28-10-3-2-4-21(28)25-15)9-13-27-11-7-16(8-12-27)22-19-6-5-17(24)14-20(19)30-26-22/h5-6,14,16H,2-4,7-13H2,1H3\",[C][C][=C][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][O][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch2][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][=N][Ring2][Ring1][=N],\"3-[2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl]-2-methyl-6,7,8,9-tetrahydropyrido[2,1-b]pyrimidin-4-one\",2.05\nCc1nc(CS(=O)(=O)c2ccc(Cl)cc2)cc(n1)N3CCOCC3,\"InChI=1S/C16H18ClN3O3S/c1-12-18-14(10-16(19-12)20-6-8-23-9-7-20)11-24(21,22)15-4-2-13(17)3-5-15/h2-5,10H,6-9,11H2,1H3\",[C][C][=N][C][Branch2][Ring1][Ring2][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][C][=Branch1][Ring2][=N][Ring1][P][N][C][C][O][C][C][Ring1][=Branch1],4-[(4-chlorophenyl)sulfonylmethyl]-2-methyl-6-morpholin-4-ylpyrimidine,1.8\nCOc1c(N2CCNC(C)C2)c(F)cc3C(=O)C(=CN(C4CC4)c13)C(=O)O,\"InChI=1S/C19H22FN3O4/c1-10-8-22(6-5-21-10)16-14(20)7-12-15(18(16)27-2)23(11-3-4-11)9-13(17(12)24)19(25)26/h7,9-11,21H,3-6,8H2,1-2H3,(H,25,26)\",[C][O][C][=C][Branch1][N][N][C][C][N][C][Branch1][C][C][C][Ring1][#Branch1][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=Branch1][S][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring2][Ring1][=Branch1][=Ring1][#Branch2][C][=Branch1][C][=O][O],1-cyclopropyl-6-fluoro-8-methoxy-7-(3-methylpiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid,-0.82\nCCCCCCCN(CC)CCCC(O)c1ccc(NS(=O)(=O)C)cc1,\"InChI=1S/C20H36N2O3S/c1-4-6-7-8-9-16-22(5-2)17-10-11-20(23)18-12-14-19(15-13-18)21-26(3,24)25/h12-15,20-21,23H,4-11,16-17H2,1-3H3\",[C][C][C][C][C][C][C][N][Branch1][Ring1][C][C][C][C][C][C][Branch1][C][O][C][=C][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][Ring1][O],n-[4-[4-(ethyl-heptylamino)-1-hydroxybutyl]phenyl]methanesulfonamide,1.2\nC[C@]12CCC(=O)C=C1C=C[C@@H]3[C@@H]2CC[C@@]4(C)[C@H]3CC[C@@]45CCC(=O)O5,\"InChI=1S/C22H28O3/c1-20-9-5-15(23)13-14(20)3-4-16-17(20)6-10-21(2)18(16)7-11-22(21)12-8-19(24)25-22/h3-4,13,16-18H,5-12H2,1-2H3/t16-,17+,18+,20+,21+,22-/m1/s1\",[C][C@][C][C][C][=Branch1][C][=O][C][=C][Ring1][#Branch1][C][=C][C@@H1][C@@H1][Ring1][O][C][C][C@@][Branch1][C][C][C@H1][Ring1][#Branch1][C][C][C@@][Ring1][=Branch1][C][C][C][=Branch1][C][=O][O][Ring1][=Branch1],\"(8r,9s,10r,13s,14s,17r)-10,13-dimethylspiro[2,8,9,11,12,14,15,16-octahydro-1h-cyclopenta[a]phenanthrene-17,5'-oxolane]-2',3-dione\",3.2\nCc1ccc2c(c1)c(Sc3cccc(Cl)c3)c(C)n2CC(=O)O,\"InChI=1S/C18H16ClNO2S/c1-11-6-7-16-15(8-11)18(12(2)20(16)10-17(21)22)23-14-5-3-4-13(19)9-14/h3-9H,10H2,1-2H3,(H,21,22)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O],\"2-[3-(3-chlorophenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\",1.85\nCC[C@H](NC(=O)c1c(O)c(nc2ccccc12)c3ccccc3)c4ccccc4,\"InChI=1S/C25H22N2O2/c1-2-20(17-11-5-3-6-12-17)27-25(29)22-19-15-9-10-16-21(19)26-23(24(22)28)18-13-7-4-8-14-18/h3-16,20,28H,2H2,1H3,(H,27,29)/t20-/m0/s1\",[C][C][C@H1][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-hydroxy-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,3.91\nOC(=O)COc1ccc(cc1c2ccc(Cl)cc2)C(F)(F)F,\"InChI=1S/C15H10ClF3O3/c16-11-4-1-9(2-5-11)12-7-10(15(17,18)19)3-6-13(12)22-8-14(20)21/h1-7H,8H2,(H,20,21)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][S][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F],2-[2-(4-chlorophenyl)-4-(trifluoromethyl)phenoxy]acetic acid,0.9\nCC(O)(C(=O)c1ccccc1)c2ccccc2,\"InChI=1S/C15H14O2/c1-15(17,13-10-6-3-7-11-13)14(16)12-8-4-2-5-9-12/h2-11,17H,1H3\",[C][C][Branch1][C][O][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-hydroxy-1,2-di(phenyl)propan-1-one\",2.92\nC[C@@H](c1ncncc1F)[C@](O)(Cn2cncn2)c3ccc(F)cc3F,\"InChI=1S/C16H14F3N5O/c1-10(15-14(19)5-20-7-22-15)16(25,6-24-9-21-8-23-24)12-3-2-11(17)4-13(12)18/h2-5,7-10,25H,6H2,1H3/t10-,16+/m0/s1\",[C][C@@H1][Branch1][#Branch2][C][=N][C][=N][C][=C][Ring1][=Branch1][F][C@][Branch1][C][O][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F],\"(2r,3s)-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol\",1.7\nCOC1=CC=C2C(=CC1=O)C(CCc3cc(OC)c(OC)c(OC)c23)NC(=O)C,\"InChI=1S/C22H25NO6/c1-12(24)23-16-8-6-13-10-19(27-3)21(28-4)22(29-5)20(13)14-7-9-18(26-2)17(25)11-15(14)16/h7,9-11,16H,6,8H2,1-5H3,(H,23,24)\",[C][O][C][=C][C][=C][C][=Branch1][=Branch1][=C][C][Ring1][#Branch1][=O][C][Branch2][Ring1][#Branch2][C][C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][Ring2][Ring1][N][N][C][=Branch1][C][=O][C],\"n-(1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5h-benzo[d]heptalen-7-yl)acetamide\",1.12\nCS(=O)(=O)c1ccc(C(=O)Nc2ccc(Cl)c(c2)c3ccccn3)c(Cl)c1,\"InChI=1S/C19H14Cl2N2O3S/c1-27(25,26)13-6-7-14(17(21)11-13)19(24)23-12-5-8-16(20)15(10-12)18-4-2-3-9-22-18/h2-11H,1H3,(H,23,24)\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][#Branch1],2-chloro-n-(4-chloro-3-pyridin-2-ylphenyl)-4-methylsulfonylbenzamide,2.84\nO=C(Nc1ccccc1)c2ccccc2,\"InChI=1S/C13H11NO/c15-13(11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h1-10H,(H,14,15)\",[O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-phenylbenzamide,2.8\nCCC(CO)NCCNC(CC)CO,\"InChI=1S/C10H24N2O2/c1-3-9(7-13)11-5-6-12-10(4-2)8-14/h9-14H,3-8H2,1-2H3\",[C][C][C][Branch1][Ring1][C][O][N][C][C][N][C][Branch1][Ring1][C][C][C][O],2-[2-(1-hydroxybutan-2-ylamino)ethylamino]butan-1-ol,-1.42\nCCCNC(=O)NS(=O)(=O)c1ccc(Cl)cc1,\"InChI=1S/C10H13ClN2O3S/c1-2-7-12-10(14)13-17(15,16)9-5-3-8(11)4-6-9/h3-6H,2,7H2,1H3,(H2,12,13,14)\",[C][C][C][N][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],1-(4-chlorophenyl)sulfonyl-3-propylurea,-0.33\nCCN1CCO[C@@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1,\"InChI=1S/C18H26Cl2N4O2/c1-2-22-9-10-26-15(12-22)13-23-5-7-24(8-6-23)18(25)21-14-3-4-16(19)17(20)11-14/h3-4,11,15H,2,5-10,12-13H2,1H3,(H,21,25)/t15-/m1/s1\",[C][C][N][C][C][O][C@@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2],\"n-(3,4-dichlorophenyl)-4-[[(2s)-4-ethylmorpholin-2-yl]methyl]piperazine-1-carboxamide\",2.68\nCOC[C@H](N1CCN(C[C@@H]1C)C2(C)CCN(CC2)C(=O)c3c(C)ncnc3C)c4ccc(cc4)C(F)(F)F,\"InChI=1S/C28H38F3N5O2/c1-19-16-35(14-15-36(19)24(17-38-5)22-6-8-23(9-7-22)28(29,30)31)27(4)10-12-34(13-11-27)26(37)25-20(2)32-18-33-21(25)3/h6-9,18-19,24H,10-17H2,1-5H3/t19-,24-/m0/s1\",[C][O][C][C@H1][Branch2][Ring2][=Branch2][N][C][C][N][Branch1][=Branch1][C][C@@H1][Ring1][=Branch1][C][C][Branch1][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][=C][N][=C][Ring1][#Branch1][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"(4,6-dimethylpyrimidin-5-yl)-[4-[(3s)-4-[(1r)-2-methoxy-1-[4-(trifluoromethyl)phenyl]ethyl]-3-methylpiperazin-1-yl]-4-methylpiperidin-1-yl]methanone\",2.7\nCOc1ccc(cc1OC)S(=O)(=O)Nc2ccc(\\C=C\\C(=O)Nc3ccccc3N)cc2,\"InChI=1S/C23H23N3O5S/c1-30-21-13-12-18(15-22(21)31-2)32(28,29)26-17-10-7-16(8-11-17)9-14-23(27)25-20-6-4-3-5-19(20)24/h3-15,26H,24H2,1-2H3,(H,25,27)/b14-9+\",[C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch1][P][\\C][=C][\\C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][Ring2][Ring1][C],\"(e)-n-(2-aminophenyl)-3-[4-[(3,4-dimethoxyphenyl)sulfonylamino]phenyl]prop-2-enamide\",2.56\nOC(=O)C(N1CCC(CC1)N2CCC(CC2)Oc3ccc(Cl)c(Cl)c3)c4ccccc4,\"InChI=1S/C24H28Cl2N2O3/c25-21-7-6-20(16-22(21)26)31-19-10-14-27(15-11-19)18-8-12-28(13-9-18)23(24(29)30)17-4-2-1-3-5-17/h1-7,16,18-19,23H,8-15H2,(H,29,30)\",[O][C][=Branch1][C][=O][C][Branch2][Ring2][Ring2][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidin-1-yl]-2-phenylacetic acid\",2.23\nC[C@H]1C[C@H]2[C@@H]3CC[C@](O)(C(=O)C)[C@@]3(C)C[C@H](O)[C@]2(F)[C@@]4(C)C=CC(=O)C=C14,\"InChI=1S/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3/t12-,15-,17-,18-,19-,20-,21-,22-/m0/s1\",[C][C@H1][C][C@H1][C@@H1][C][C][C@][Branch1][C][O][Branch1][=Branch1][C][=Branch1][C][=O][C][C@@][Ring1][=Branch2][Branch1][C][C][C][C@H1][Branch1][C][O][C@][Ring1][#C][Branch1][C][F][C@@][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2],\"(6s,8s,9r,10s,11s,13s,14s,17r)-17-acetyl-9-fluoro-11,17-dihydroxy-6,10,13-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one\",2.65\nClc1ccccc1CNC(=O)c2ccccc2Oc3ccccc3,\"InChI=1S/C20H16ClNO2/c21-18-12-6-4-8-15(18)14-22-20(23)17-11-5-7-13-19(17)24-16-9-2-1-3-10-16/h1-13H,14H2,(H,22,23)\",[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1],n-[(2-chlorophenyl)methyl]-2-(phenoxy)benzamide,3.58\nCC1(COc2ccc3c(c2)ncn3c4ccc5cccc(N6CCC(N)CC6)c5n4)COC1,\"InChI=1S/C26H29N5O2/c1-26(14-32-15-26)16-33-20-6-7-22-21(13-20)28-17-31(22)24-8-5-18-3-2-4-23(25(18)29-24)30-11-9-19(27)10-12-30/h2-8,13,17,19H,9-12,14-16,27H2,1H3\",[C][C][Branch2][Ring2][=N][C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=C][N][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Branch1][N][N][C][C][C][Branch1][C][N][C][C][Ring1][#Branch1][C][Ring1][=N][=N][Ring1][P][C][O][C][Ring2][Ring1][S],1-[2-[5-[(3-methyloxetan-3-yl)methoxy]benzimidazol-1-yl]quinolin-8-yl]piperidin-4-amine,1.99\nOC1(CCN(CCCC(=O)c2ccc(F)cc2)CC1)c3ccc(Cl)cc3,\"InChI=1S/C21H23ClFNO2/c22-18-7-5-17(6-8-18)21(26)11-14-24(15-12-21)13-1-2-20(25)16-3-9-19(23)10-4-16/h3-10,26H,1-2,11-15H2\",[O][C][Branch2][Ring1][=C][C][C][N][Branch2][Ring1][Ring1][C][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one,2.67\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)Cc3cccc(c3)C(=O)O)C(=O)C(F)(F)F,\"InChI=1S/C28H26F3N3O6/c1-16(2)24(25(37)28(29,30)31)33-23(36)15-34-21(18-8-4-3-5-9-18)12-11-20(26(34)38)32-22(35)14-17-7-6-10-19(13-17)27(39)40/h3-13,16,24H,14-15H2,1-2H3,(H,32,35)(H,33,36)(H,39,40)\",[C][C][Branch1][C][C][C][Branch2][Ring2][P][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"3-[2-oxo-2-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]amino]ethyl]benzoic acid\",0.68\nOC(=O)CCC(=O)c1ccc(cc1)c2ccccc2,\"InChI=1S/C16H14O3/c17-15(10-11-16(18)19)14-8-6-13(7-9-14)12-4-2-1-3-5-12/h1-9H,10-11H2,(H,18,19)\",[O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],4-oxo-4-(4-phenylphenyl)butanoic acid,0.58\nCOc1cc2c(Nc3c(Cl)ccc4OCOc34)ncnc2cc1OCC5CCN(C)CC5,\"InChI=1S/C23H25ClN4O4/c1-28-7-5-14(6-8-28)11-30-20-10-17-15(9-19(20)29-2)23(26-12-25-17)27-21-16(24)3-4-18-22(21)32-13-31-18/h3-4,9-10,12,14H,5-8,11,13H2,1-2H3,(H,25,26,27)\",[C][O][C][=C][C][=C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][N][=C][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],\"n-(5-chloro-1,3-benzodioxol-4-yl)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinazolin-4-amine\",1.83\nNS(=O)(=O)c1cc(ccc1Cl)C2(O)NC(=O)c3ccccc23,\"InChI=1S/C14H11ClN2O4S/c15-11-6-5-8(7-12(11)22(16,20)21)14(19)10-4-2-1-3-9(10)13(18)17-14/h1-7,19H,(H,17,18)(H2,16,20,21)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1],2-chloro-5-(1-hydroxy-3-oxo-2h-isoindol-1-yl)benzenesulfonamide,0.97\nCOc1ccc2nc(NC(=O)CCc3ccc(OC)c(OC)c3)sc2c1,\"InChI=1S/C19H20N2O4S/c1-23-13-6-7-14-17(11-13)26-19(20-14)21-18(22)9-5-12-4-8-15(24-2)16(10-12)25-3/h4,6-8,10-11H,5,9H2,1-3H3,(H,20,21,22)\",[C][O][C][=C][C][=C][N][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][C][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][S][C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2],\"3-(3,4-dimethoxyphenyl)-n-(6-methoxy-1,3-benzothiazol-2-yl)propanamide\",3.57\nCC(C)n1c(C)ncc1c2nc(Nc3ccc(C(=O)NCCN(C)C)c(F)c3)ncc2F,\"InChI=1S/C22H27F2N7O/c1-13(2)31-14(3)26-12-19(31)20-18(24)11-27-22(29-20)28-15-6-7-16(17(23)10-15)21(32)25-8-9-30(4)5/h6-7,10-13H,8-9H2,1-5H3,(H,25,32)(H,27,28,29)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][=N][C][=Branch1][C][=O][N][C][C][N][Branch1][C][C][C][C][Branch1][C][F][=C][Ring1][#C][=N][C][=C][Ring2][Ring1][=Branch1][F],n-(2-dimethylaminoethyl)-2-fluoro-4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide,2.26\nCN1CCN(CC1)C(=O)c2cc3cc(C)ccc3[nH]2,\"InChI=1S/C15H19N3O/c1-11-3-4-13-12(9-11)10-14(16-13)15(19)18-7-5-17(2)6-8-18/h3-4,9-10,16H,5-8H2,1-2H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],(5-methyl-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone,2.22\nCNc1cccc(CCCc2ccc(C[C@H](NC(=O)c3c(Cl)cccc3Cl)C(=O)O)s2)n1,\"InChI=1S/C23H23Cl2N3O3S/c1-26-20-10-3-6-14(27-20)5-2-7-15-11-12-16(32-15)13-19(23(30)31)28-22(29)21-17(24)8-4-9-18(21)25/h3-4,6,8-12,19H,2,5,7,13H2,1H3,(H,26,27)(H,28,29)(H,30,31)/t19-/m0/s1\",[C][N][C][=C][C][=C][C][Branch2][Ring2][#Branch2][C][C][C][C][=C][C][=C][Branch2][Ring1][N][C][C@H1][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=Branch1][C][=O][O][S][Ring2][Ring1][Branch1][=N][Ring2][Ring1][=C],\"(2s)-2-[(2,6-dichlorobenzoyl)amino]-3-[5-[3-(6-methylaminopyridin-2-yl)propyl]thiophen-2-yl]propanoic acid\",0.78\nCC(C)(C(=O)c1cccnc1)c2cccnc2,\"InChI=1S/C14H14N2O/c1-14(2,12-6-4-8-16-10-12)13(17)11-5-3-7-15-9-11/h3-10H,1-2H3\",[C][C][Branch1][C][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],\"2-methyl-1,2-di(pyridin-3-yl)propan-1-one\",1.45\nCNC(=O)c1ccc(Oc2ccc3CCN(CCc3c2)C4CCC4)nc1,\"InChI=1S/C21H25N3O2/c1-22-21(25)17-6-8-20(23-14-17)26-19-7-5-15-9-11-24(18-3-2-4-18)12-10-16(15)13-19/h5-8,13-14,18H,2-4,9-12H2,1H3,(H,22,25)\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][O][C][=C][C][=C][C][C][N][Branch1][=Branch2][C][C][C][Ring1][#Branch1][=C][Ring1][O][C][C][C][C][Ring1][Ring2][N][=C][Ring2][Ring1][=Branch1],\"6-[(3-cyclobutyl-1,2,4,5-tetrahydro-3-benzazepin-8-yl)oxy]-n-methylpyridine-3-carboxamide\",1.45\nOC1N=C(c2ccccc2Cl)c3cc(Cl)ccc3NC1=O,\"InChI=1S/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)\",[O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][C][Ring2][Ring1][Ring1][=O],\"7-chloro-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-1,4-benzodiazepin-2-one\",2.38\nCCCNC(=O)c1nnc2c(cccc2c1N)c3cncc(c3)C(=O)N4CCC4,\"InChI=1S/C21H22N6O2/c1-2-7-24-20(28)19-17(22)16-6-3-5-15(18(16)25-26-19)13-10-14(12-23-11-13)21(29)27-8-4-9-27/h3,5-6,10-12H,2,4,7-9H2,1H3,(H2,22,25)(H,24,28)\",[C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring2],4-amino-8-[5-(azetidine-1-carbonyl)pyridin-3-yl]-n-propylcinnoline-3-carboxamide,2.79\nCN(C)CCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4cccnn34)cc1,\"InChI=1S/C21H24N8O2S/c1-28(2)14-4-12-25-32(30,31)17-8-6-16(7-9-17)26-21-22-13-10-18(27-21)19-15-23-20-5-3-11-24-29(19)20/h3,5-11,13,15,25H,4,12,14H2,1-2H3,(H,22,26,27)\",[C][N][Branch1][C][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=N][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"n-(3-dimethylaminopropyl)-4-[(4-imidazo[2,3-f]pyridazin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\",1.4\nNc1c2CCCCc2nc3ccccc13,\"InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)\",[N][C][=C][C][C][C][C][C][Ring1][=Branch1][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1],\"1,2,3,4-tetrahydroacridin-9-amine\",0.38\nO=C(C1CCN(CC1)c2nnc(s2)n3cccc3)N4CCc5ccccc5C4,\"InChI=1S/C21H23N5OS/c27-19(26-14-7-16-5-1-2-6-18(16)15-26)17-8-12-25(13-9-17)21-23-22-20(28-21)24-10-3-4-11-24/h1-6,10-11,17H,7-9,12-15H2\",[O][=C][Branch2][Ring1][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][N][C][=C][C][=C][Ring1][Branch1][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2],\"3,4-dihydro-1h-isoquinolin-2-yl-[1-(5-pyrrol-1-yl-1,3,4-thiadiazol-2-yl)piperidin-4-yl]methanone\",3.7\nCOc1ccc(CN2CCc3c(C2)[nH]c4ccccc34)cc1OC,\"InChI=1S/C20H22N2O2/c1-23-19-8-7-14(11-20(19)24-2)12-22-10-9-16-15-5-3-4-6-17(15)21-18(16)13-22/h3-8,11,21H,9-10,12-13H2,1-2H3\",[C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][C][N][C][C][C][=C][Branch1][Ring2][C][Ring1][=Branch1][NH1][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring2][O][C],\"2-[(3,4-dimethoxyphenyl)methyl]-1,3,4,9-tetrahydropyrido[3,4-b]indole\",3.1\nCNC1=Nc2ncccc2C(=NC1c3cccs3)c4cccs4,\"InChI=1S/C17H14N4S2/c1-18-17-15(13-7-4-10-23-13)20-14(12-6-3-9-22-12)11-5-2-8-19-16(11)21-17/h2-10,15H,1H3,(H,18,19,21)\",[C][N][C][=N][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][N][=N][C][Ring1][O][C][=C][C][=C][S][Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1],\"n-methyl-3,5-di(thiophen-2-yl)-3h-pyrido[3,2-f][1,4]diazepin-2-amine\",2.63\nClc1ccc2NC(=O)CN(C(c3ccccc3)c2c1)C(=O)c4occc4,\"InChI=1S/C20H15ClN2O3/c21-14-8-9-16-15(11-14)19(13-5-2-1-3-6-13)23(12-18(24)22-16)20(25)17-7-4-10-26-17/h1-11,19H,12H2,(H,22,24)\",[Cl][C][=C][C][=C][N][C][=Branch1][C][=O][C][N][Branch2][Ring1][Ring1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=C][=C][Ring2][Ring1][C][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1],\"7-chloro-4-(furan-2-carbonyl)-5-phenyl-3,5-dihydro-1h-1,4-benzodiazepin-2-one\",3\nCC1=CC2=NNC(=O)N2c3ccccc13,\"InChI=1S/C11H9N3O/c1-7-6-10-12-13-11(15)14(10)9-5-3-2-4-8(7)9/h2-6H,1H3,(H,13,15)\",[C][C][=C][C][=N][N][C][=Branch1][C][=O][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1],\"5-methyl-2h-[1,2,4]triazolo[4,5-a]quinolin-1-one\",2.35\nCC1=C(OCc2ccccc2)C(=O)C=CO1,\"InChI=1S/C13H12O3/c1-10-13(12(14)7-8-15-10)16-9-11-5-3-2-4-6-11/h2-8H,9H2,1H3\",[C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][O][Ring1][#C],2-methyl-3-(phenylmethoxy)pyran-4-one,1.87\nO=C(CC12CC3CC(CC(C3)C1)C2)Nc4cccc5ncccc45,\"InChI=1S/C21H24N2O/c24-20(23-19-5-1-4-18-17(19)3-2-6-22-18)13-21-10-14-7-15(11-21)9-16(8-14)12-21/h1-6,14-16H,7-13H2,(H,23,24)\",[O][=C][Branch2][Ring1][=Branch1][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][C][=C][C][=C][C][=N][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],2-(1-adamantyl)-n-quinolin-5-ylacetamide,3.83\nO=C1C(=O)c2cccnc2c3ccccc13,InChI=1S/C13H7NO2/c15-12-9-5-2-1-4-8(9)11-10(13(12)16)6-3-7-14-11/h1-7H,[O][=C][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"benzo[h]quinoline-5,6-dione\",1.88\nCOc1ccccc1OCC(O)CO,\"InChI=1S/C10H14O4/c1-13-9-4-2-3-5-10(9)14-7-8(12)6-11/h2-5,8,11-12H,6-7H2,1H3\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O],\"3-(2-methoxyphenoxy)propane-1,2-diol\",0.24\nCCc1cccc2c3CCOC(CC)(CC(=O)O)c3[nH]c12,\"InChI=1S/C17H21NO3/c1-3-11-6-5-7-12-13-8-9-21-17(4-2,10-14(19)20)16(13)18-15(11)12/h5-7,18H,3-4,8-10H2,1-2H3,(H,19,20)\",[C][C][C][=C][C][=C][C][C][C][C][O][C][Branch1][Ring1][C][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=Ring1][N][NH1][C][Ring2][Ring1][Ring1][=Ring1][#C],\"2-(1,8-diethyl-4,9-dihydro-3h-pyrano[3,4-b]indol-1-yl)acetic acid\",0.49\nCN1CC(c2ccccc2)c3cccc(N)c3C1,\"InChI=1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3\",[C][N][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1][C][Ring1][P],\"2-methyl-4-phenyl-3,4-dihydro-1h-isoquinolin-8-amine\",2.08\nNc1cccc(NC(=O)c2ccc(CNC(=O)OCc3cccnc3)cc2)c1,\"InChI=1S/C21H20N4O3/c22-18-4-1-5-19(11-18)25-20(26)17-8-6-15(7-9-17)13-24-21(27)28-14-16-3-2-10-23-12-16/h1-12H,13-14,22H2,(H,24,27)(H,25,26)\",[N][C][=C][C][=C][C][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][P][C][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][C][=C][Ring2][Ring1][O],pyridin-3-ylmethyl n-[[4-[(3-aminophenyl)carbamoyl]phenyl]methyl]carbamate,1.6\nCC(NC(C)(C)C)C(=O)c1cccc(Cl)c1,\"InChI=1S/C13H18ClNO/c1-9(15-13(2,3)4)12(16)10-6-5-7-11(14)8-10/h5-9,15H,1-4H3\",[C][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],2-(tert-butylamino)-1-(3-chlorophenyl)propan-1-one,2.12\nCC1=CC(=O)Oc2c3CCCNc3c(C)cc12,\"InChI=1S/C14H15NO2/c1-8-7-12(16)17-14-10-4-3-5-15-13(10)9(2)6-11(8)14/h6-7,15H,3-5H2,1-2H3\",[C][C][=C][C][=Branch1][C][=O][O][C][=C][C][C][C][N][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][Ring1][S][Ring1][O],\"4,6-dimethyl-7,8,9,10-tetrahydropyrano[6,5-f]quinolin-2-one\",2.9\nNC(=O)c1cnc(N[C@H]2CCCNC2)c3cc(sc13)c4ccc(F)cc4,\"InChI=1S/C19H19FN4OS/c20-12-5-3-11(4-6-12)16-8-14-17(26-16)15(18(21)25)10-23-19(14)24-13-2-1-7-22-9-13/h3-6,8,10,13,22H,1-2,7,9H2,(H2,21,25)(H,23,24)/t13-/m0/s1\",[N][C][=Branch1][C][=O][C][=C][N][=C][Branch1][#Branch2][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][C][=C][Branch1][#Branch1][S][C][Ring1][S][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"2-(4-fluorophenyl)-4-[[(3s)-piperidin-3-yl]amino]thieno[2,3-d]pyridine-7-carboxamide\",2.01\nCc1c(Sc2ccc(Cl)cc2)c3cccc(Cl)c3n1CC(=O)O,\"InChI=1S/C17H13Cl2NO2S/c1-10-17(23-12-7-5-11(18)6-8-12)13-3-2-4-14(19)16(13)20(10)9-15(21)22/h2-8H,9H2,1H3,(H,21,22)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],2-[7-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid,2\nOC(CCN1CCCCC1)(C2CCCCC2)c3ccccc3,\"InChI=1S/C20H31NO/c22-20(18-10-4-1-5-11-18,19-12-6-2-7-13-19)14-17-21-15-8-3-9-16-21/h1,4-5,10-11,19,22H,2-3,6-9,12-17H2\",[O][C][Branch1][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol,2.68\nFc1ccc(N2CCN(CC2)C(=O)COCc3ccncc3)c(Cl)c1,\"InChI=1S/C18H19ClFN3O2/c19-16-11-15(20)1-2-17(16)22-7-9-23(10-8-22)18(24)13-25-12-14-3-5-21-6-4-14/h1-6,11H,7-10,12-13H2\",[F][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2],1-[4-(2-chloro-4-fluorophenyl)piperazin-1-yl]-2-(pyridin-4-ylmethoxy)ethanone,2.63\nNc1ncnc2nc(cc(c3cccc(Br)c3)c12)c4ccc(nc4)N5CCOCC5,\"InChI=1S/C22H19BrN6O/c23-16-3-1-2-14(10-16)17-11-18(28-22-20(17)21(24)26-13-27-22)15-4-5-19(25-12-15)29-6-8-30-9-7-29/h1-5,10-13H,6-9H2,(H2,24,26,27,28)\",[N][C][=N][C][=N][C][=N][C][=Branch2][Ring1][Branch1][=C][C][Branch1][N][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1][=C][Ring1][P][Ring1][=N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"5-(3-bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[3,2-e]pyrimidin-4-amine\",3.2\nCC1=CN(Cc2ccccc2)C(=O)NC1=O,\"InChI=1S/C12H12N2O2/c1-9-7-14(12(16)13-11(9)15)8-10-5-3-2-4-6-10/h2-7H,8H2,1H3,(H,13,15,16)\",[C][C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][Ring1][=C][=O],\"5-methyl-1-(phenylmethyl)pyrimidine-2,4-dione\",1.19\nClc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4cocc4)C3=O,\"InChI=1S/C16H10ClN3O4/c17-9-1-2-10-11(5-9)18-13-12(14(10)21)16(23)20(19-15(13)22)6-8-3-4-24-7-8/h1-5,7H,6H2,(H,18,21)(H,19,22)\",[Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][=Branch2][C][C][=C][O][C][=C][Ring1][Branch1][C][Ring1][S][=O],\"7-chloro-2-(furan-3-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",0.6\nNc1nc2ccccc2n1C(=O)c3ccccc3,\"InChI=1S/C14H11N3O/c15-14-16-11-8-4-5-9-12(11)17(14)13(18)10-6-2-1-3-7-10/h1-9H,(H2,15,16)\",[N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],(2-aminobenzimidazol-1-yl)-phenylmethanone,1.56\nCC(=O)N1CCN(CC1)c2ccc(OCC3COC(Cn4ccnc4)(O3)c5ccc(Cl)cc5Cl)cc2,\"InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3\",[C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring2][C][O][C][C][C][O][C][Branch1][=Branch2][C][N][C][=C][N][=C][Ring1][Branch1][Branch1][Ring2][O][Ring1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][C][=C][Ring2][Ring1][O],\"1-[4-[4-[[2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]ethanone\",3.7\nCCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cccc(Cl)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H39ClN2O5S2/c1-4-35(32(36)22-24-8-12-29(13-9-24)41(2,37)38)28-16-19-34(20-17-28)21-18-31(26-6-5-7-27(33)23-26)25-10-14-30(15-11-25)42(3,39)40/h5-15,23,28,31H,4,16-22H2,1-3H3/t31-/m1/s1\",[C][C][N][Branch2][Ring2][S][C][C][C][N][Branch2][Ring2][Ring2][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-[1-[(3r)-3-(3-chlorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide,2.37\nCC(C)OC(=O)N1CCC(CC1)Oc2ncnc(Oc3cccnc3C)c2C,\"InChI=1S/C20H26N4O4/c1-13(2)26-20(25)24-10-7-16(8-11-24)27-18-14(3)19(23-12-22-18)28-17-6-5-9-21-15(17)4/h5-6,9,12-13,16H,7-8,10-11H2,1-4H3\",[C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][Branch1][O][O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring1][=C][C],propan-2-yl 4-[5-methyl-6-(2-methylpyridin-3-yl)oxypyrimidin-4-yl]oxypiperidine-1-carboxylate,3.8\nCc1ncc2CN=C(c3ccccc3F)c4cc(Cl)ccc4n12,\"InChI=1S/C18H13ClFN3/c1-11-21-9-13-10-22-18(14-4-2-3-5-16(14)20)15-8-12(19)6-7-17(15)23(11)13/h2-9H,10H2,1H3\",[C][C][=N][C][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1],\"8-chloro-6-(2-fluorophenyl)-1-methyl-4h-imidazo[1,5-a][1,4]benzodiazepine\",3.4\nCN1C(=O)c2c(onc2c3ccncc3)C=C1c4ccccc4,\"InChI=1S/C18H13N3O2/c1-21-14(12-5-3-2-4-6-12)11-15-16(18(21)22)17(20-23-15)13-7-9-19-10-8-13/h2-11H,1H3\",[C][N][C][=Branch1][C][=O][C][=C][Branch1][=C][O][N][=C][Ring1][Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-methyl-6-phenyl-3-pyridin-4-yl-[1,2]oxazolo[4,5-c]pyridin-4-one\",3.17\nCc1cc(N)n(n1)c2ccccc2,\"InChI=1S/C10H11N3/c1-8-7-10(11)13(12-8)9-5-3-2-4-6-9/h2-7H,11H2,1H3\",[C][C][C][=C][Branch1][C][N][N][Branch1][Ring2][N][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],5-methyl-2-phenylpyrazol-3-amine,1.25\nOC(=O)C[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4cc(F)ccc4[nH]3,\"InChI=1S/C20H17FN2O3/c21-13-5-6-16-12(7-13)9-18(22-16)20(26)23-17-8-11-3-1-2-4-14(11)15(17)10-19(24)25/h1-7,9,15,17,22H,8,10H2,(H,23,26)(H,24,25)/t15-,17-/m1/s1\",[O][C][=Branch1][C][=O][C][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],\"2-[(1r,2r)-2-[(5-fluoro1h-indole-2-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]acetic acid\",1.26\nNS(=O)(=O)c1cc2c(NCNS2(=O)=O)cc1Cl,\"InChI=1S/C7H8ClN3O4S2/c8-4-1-5-7(2-6(4)16(9,12)13)17(14,15)11-3-10-5/h1-2,10-11H,3H2,(H2,9,12,13)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][O][N][C][N][S][Ring1][=Branch1][=Branch1][C][=O][=O][C][=C][Ring1][N][Cl],\"6-chloro-1,1-dioxo-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\",-0.09\nCC(=O)N1CCN(CC(O)COc2ccc(Br)cc2)CC1,\"InChI=1S/C15H21BrN2O3/c1-12(19)18-8-6-17(7-9-18)10-14(20)11-21-15-4-2-13(16)3-5-15/h2-5,14,20H,6-11H2,1H3\",[C][C][=Branch1][C][=O][N][C][C][N][Branch2][Ring1][Ring1][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][C],1-[4-[3-(4-bromophenoxy)-2-hydroxypropyl]piperazin-1-yl]ethanone,1.6\nClc1ccc(cc1Cl)C2=CSC3=NCCN23,\"InChI=1S/C11H8Cl2N2S/c12-8-2-1-7(5-9(8)13)10-6-16-11-14-3-4-15(10)11/h1-2,5-6H,3-4H2\",[Cl][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][=C][S][C][=N][C][C][N][Ring1][Branch2][Ring1][Branch1],\"3-(3,4-dichlorophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole\",1.54\nCC(C)N(C(C)C)C(=O)C(C(CNC(=O)NCc1ccccc1F)c2ccccc2)c3cccnc3,\"InChI=1S/C29H35FN4O2/c1-20(2)34(21(3)4)28(35)27(24-14-10-16-31-17-24)25(22-11-6-5-7-12-22)19-33-29(36)32-18-23-13-8-9-15-26(23)30/h5-17,20-21,25,27H,18-19H2,1-4H3,(H2,32,33,36)\",[C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch2][Ring1][=C][C][Branch2][Ring1][C][C][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],\"4-[(2-fluorophenyl)methylcarbamoylamino]-3-phenyl-n,n-di(propan-2-yl)-2-pyridin-3-ylbutanamide\",4.2\nCc1sc(CN2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C22H33N3OS/c1-15-20(9-19(27-15)13-25-4-2-23-3-5-25)21(26)24-14-22-10-16-6-17(11-22)8-18(7-16)12-22/h9,16-18,23H,2-8,10-14H2,1H3,(H,24,26)\",[C][C][S][C][Branch1][#Branch2][C][N][C][C][N][C][C][Ring1][=Branch1][=C][C][=Ring1][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-methyl-5-(piperazin-1-ylmethyl)thiophene-3-carboxamide,2.55\nCc1cc(CCCOc2c(C)cc(cc2C)c3noc(n3)C(F)(F)F)on1,\"InChI=1S/C18H18F3N3O3/c1-10-7-13(16-22-17(27-24-16)18(19,20)21)8-11(2)15(10)25-6-4-5-14-9-12(3)23-26-14/h7-9H,4-6H2,1-3H3\",[C][C][C][=C][Branch2][Ring2][Ring2][C][C][C][O][C][=C][Branch1][C][C][C][=C][Branch1][=Branch1][C][=C][Ring1][#Branch1][C][C][=N][O][C][=Branch1][Ring2][=N][Ring1][Branch1][C][Branch1][C][F][Branch1][C][F][F][O][N][=Ring2][Ring1][#Branch2],\"3-[3,5-dimethyl-4-[3-(3-methyl-1,2-oxazol-5-yl)propoxy]phenyl]-5-(trifluoromethyl)-1,2,4-oxadiazole\",3.63\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccccc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C26H25F3N4O5/c1-16(2)21(22(35)26(27,28)29)32-20(34)14-33-23(18-11-7-4-8-12-18)30-13-19(24(33)36)31-25(37)38-15-17-9-5-3-6-10-17/h3-13,16,21H,14-15H2,1-2H3,(H,31,37)(H,32,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-phenylpyrimidin-5-yl]carbamate\",2.12\nCN1C(C(=O)Nc2ncc(C)s2)C(=O)c3ccccc3S1(=O)=O,\"InChI=1S/C14H13N3O4S2/c1-8-7-15-14(22-8)16-13(19)11-12(18)9-5-3-4-6-10(9)23(20,21)17(11)2/h3-7,11H,1-2H3,(H,15,16,19)\",[C][N][C][Branch1][S][C][=Branch1][C][=O][N][C][=N][C][=C][Branch1][C][C][S][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring2][Ring1][Ring2][=Branch1][C][=O][=O],\"2-methyl-n-(5-methyl-1,3-thiazol-2-yl)-1,1,4-trioxo-3h-benzo[e]thiazine-3-carboxamide\",0.3\nCCN1C=C(C(=O)O)C(=O)c2cc(F)c(nc12)N3CCNCC3,\"InChI=1S/C15H17FN4O3/c1-2-19-8-10(15(22)23)12(21)9-7-11(16)14(18-13(9)19)20-5-3-17-4-6-20/h7-8,17H,2-6H2,1H3,(H,22,23)\",[C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][Branch1][#Branch1][N][=C][Ring1][#C][Ring1][#Branch1][N][C][C][N][C][C][Ring1][=Branch1],\"1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,8-naphthyridine-3-carboxylic acid\",-0.83\nCOc1cc(N2CCCN(C)CC2)c3NC(=CC(=O)c3c1)C(=O)Nc4ccc(cc4)N5CCOCC5,\"InChI=1S/C27H33N5O4/c1-30-8-3-9-32(11-10-30)24-17-21(35-2)16-22-25(33)18-23(29-26(22)24)27(34)28-19-4-6-20(7-5-19)31-12-14-36-15-13-31/h4-7,16-18H,3,8-15H2,1-2H3,(H,28,34)(H,29,33)\",[C][O][C][=C][C][Branch1][=N][N][C][C][C][N][Branch1][C][C][C][C][Ring1][Branch2][=C][N][C][=Branch1][=N][=C][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"6-methoxy-8-(4-methyl-1,4-diazepan-1-yl)-n-(4-morpholin-4-ylphenyl)-4-oxo-1h-quinoline-2-carboxamide\",2.1\nCOc1cc2ncnc(Nc3cccc(O)c3)c2cc1OC,\"InChI=1S/C16H15N3O3/c1-21-14-7-12-13(8-15(14)22-2)17-9-18-16(12)19-10-4-3-5-11(20)6-10/h3-9,20H,1-2H3,(H,17,18,19)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1][=C][Ring1][=C][C][=C][Ring2][Ring1][C][O][C],\"3-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol\",2.6\nCCS(=O)(=O)c1ccc(c(C)c1)c2cc(Cl)ccc2OCC(=O)O,\"InChI=1S/C17H17ClO5S/c1-3-24(21,22)13-5-6-14(11(2)8-13)15-9-12(18)4-7-16(15)23-10-17(19)20/h4-9H,3,10H2,1-2H3,(H,19,20)\",[C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O],2-[4-chloro-2-(4-ethylsulfonyl-2-methylphenyl)phenoxy]acetic acid,-0.65\nFc1ccccc1Nc2oc(nn2)C(=O)Nc3ccc(cc3)N4CCOCC4,\"InChI=1S/C19H18FN5O3/c20-15-3-1-2-4-16(15)22-19-24-23-18(28-19)17(26)21-13-5-7-14(8-6-13)25-9-11-27-12-10-25/h1-8H,9-12H2,(H,21,26)(H,22,24)\",[F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"5-[(2-fluorophenyl)amino]-n-(4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\",3.05\nNc1ccc2c(c1)C(=O)C(=O)c3cc(N)ccc23,\"InChI=1S/C14H10N2O2/c15-7-1-3-9-10-4-2-8(16)6-12(10)14(18)13(17)11(9)5-7/h1-6H,15-16H2\",[N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][Branch1][C][N][=C][C][=C][Ring1][=C][Ring1][#Branch1],\"2,7-diaminophenanthrene-9,10-dione\",1.72\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)c3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C25H24F3N3O5S/c1-16(2)22(23(33)25(26,27)28)29-21(32)15-31-20(17-9-5-3-6-10-17)14-13-19(24(31)34)30-37(35,36)18-11-7-4-8-12-18/h3-14,16,22,30H,15H2,1-2H3,(H,29,32)\",[C][C][Branch1][C][C][C][Branch2][Ring2][N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-6-phenyl-3-(phenylsulfonylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.26\nCCCc1nc2c(C)cc(cc2n1Cc3ccc(cc3)c4ccccc4C(=O)O)c5nc6ccccc6n5C,\"InChI=1S/C33H30N4O2/c1-4-9-30-35-31-21(2)18-24(32-34-27-12-7-8-13-28(27)36(32)3)19-29(31)37(30)20-22-14-16-23(17-15-22)25-10-5-6-11-26(25)33(38)39/h5-8,10-19H,4,9,20H2,1-3H3,(H,38,39)\",[C][C][C][C][=N][C][=C][Branch1][C][C][C][=C][Branch2][Ring1][S][C][=C][Ring1][#Branch1][N][Ring1][#Branch2][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C],2-[4-[[4-methyl-6-(1-methylbenzimidazol-2-yl)-2-propylbenzimidazol-1-yl]methyl]phenyl]benzoic acid,2.21\nCOc1ccc2nccc([C@@H](O)[C@@H]3C[C@H]4CCN3C[C@@H]4C=C)c2c1,\"InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14+,19-,20+/m0/s1\",[C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Ring1][C@@H1][Branch1][C][O][C@@H1][C][C@H1][C][C][N][Ring1][=Branch1][C][C@@H1][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1],\"(r)-[(4r,5r,7s)-5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl]-(6-methoxyquinolin-4-yl)methanol\",2.26\nOCC(CO)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C20H20ClN3O4S/c21-17-7-13-6-14(23-19(13)29-17)18(27)22-15-5-12-3-1-2-4-16(12)24(20(15)28)8-11(9-25)10-26/h1-4,6-7,11,15,23,25-26H,5,8-10H2,(H,22,27)\",[O][C][C][Branch1][Ring1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-[3-hydroxy-2-(hydroxymethyl)propyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.56\nCS(=O)(=O)c1ccc(c[n+]1[O-])C(=O)Nc2ccc(F)cc2,\"InChI=1S/C13H11FN2O4S/c1-21(19,20)12-7-2-9(8-16(12)18)13(17)15-11-5-3-10(14)4-6-11/h2-8H,1H3,(H,15,17)\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=N+1][Ring1][=Branch1][O-1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],n-(4-fluorophenyl)-6-methylsulfonyl-1-oxidopyridin-1-ium-3-carboxamide,0.84\nNc1nccc(n1)n2ccc3ccccc23,\"InChI=1S/C12H10N4/c13-12-14-7-5-11(15-12)16-8-6-9-3-1-2-4-10(9)16/h1-8H,(H2,13,14,15)\",[N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1],4-indol-1-ylpyrimidin-2-amine,2.71\nCCN(C1CCN(CCC(N2CCC(CC2)C(=O)C)c3ccccc3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H45N3O4S/c1-4-35(32(37)24-26-10-12-30(13-11-26)40(3,38)39)29-16-19-33(20-17-29)21-18-31(28-8-6-5-7-9-28)34-22-14-27(15-23-34)25(2)36/h5-13,27,29,31H,4,14-24H2,1-3H3\",[C][C][N][Branch2][Ring2][=Branch2][C][C][C][N][Branch2][Ring1][=N][C][C][C][Branch1][S][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-[1-[3-(4-acetylpiperidin-1-yl)-3-phenylpropyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide,0.9\nCC(C)Cc1ccc(cc1)C(C)C(=O)NS(=O)(=O)C,\"InChI=1S/C14H21NO3S/c1-10(2)9-12-5-7-13(8-6-12)11(3)14(16)15-19(4,17)18/h5-8,10-11H,9H2,1-4H3,(H,15,16)\",[C][C][Branch1][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C],2-[4-(2-methylpropyl)phenyl]-n-methylsulfonylpropanamide,0.78\nCc1cc(NC(=O)c2ccccc2)n[nH]1,\"InChI=1S/C11H11N3O/c1-8-7-10(14-13-8)12-11(15)9-5-3-2-4-6-9/h2-7H,1H3,(H2,12,13,14,15)\",[C][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][NH1][Ring1][=C],n-(5-methyl-1h-pyrazol-3-yl)benzamide,1.75\nNc1nc2nc(cc(n2n1)C(F)(F)F)c3cccs3,\"InChI=1S/C10H6F3N5S/c11-10(12,13)7-4-5(6-2-1-3-19-6)15-9-16-8(14)17-18(7)9/h1-4H,(H2,14,17)\",[N][C][N][=C][N][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch1][N][Ring1][=Branch1][N][=Ring1][=Branch2][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][S][Ring1][Branch1],\"5-thiophen-2-yl-7-(trifluoromethyl)-[1,2,4]triazolo[1,5-a]pyrimidin-2-amine\",2.01\nCc1c(OCC(F)(F)F)ccnc1C[S+]([O-])c2nc3ccccc3[nH]2,\"InChI=1S/C16H14F3N3O2S/c1-10-13(20-7-6-14(10)24-9-16(17,18)19)8-25(23)15-21-11-4-2-3-5-12(11)22-15/h2-7H,8-9H2,1H3,(H,21,22)\",[C][C][=C][Branch1][O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=C][N][=C][Ring1][N][C][S+1][Branch1][C][O-1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-[[3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methylsulfinyl]-1h-benzimidazole\",2.7\nNc1nc2ccc(cc2[nH]1)C(=O)c3ccccc3,\"InChI=1S/C14H11N3O/c15-14-16-11-7-6-10(8-12(11)17-14)13(18)9-4-2-1-3-5-9/h1-8H,(H3,15,16,17)\",[N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],(2-amino-3h-benzimidazol-5-yl)-phenylmethanone,2.29\nNC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)C2(F)F,\"InChI=1S/C9H11F2N3O4/c10-9(11)6(16)4(3-15)18-7(9)14-2-1-5(12)13-8(14)17/h1-2,4,6-7,15-16H,3H2,(H2,12,13,17)/t4-,6-,7-/m1/s1\",[N][C][=N][C][=Branch1][C][=O][N][Branch1][Branch1][C][=C][Ring1][#Branch1][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C][Ring1][Branch2][Branch1][C][F][F],\"4-amino-1-[(2r,4r,5r)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one\",-1.5\nCC(C)Oc1ccc2C(=O)C(=COc2c1)c3ccccc3,\"InChI=1S/C18H16O3/c1-12(2)21-14-8-9-15-17(10-14)20-11-16(18(15)19)13-6-4-3-5-7-13/h3-12H,1-2H3\",[C][C][Branch1][C][C][O][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][C][=C][Ring1][=Branch1],3-phenyl-7-propan-2-yloxychromen-4-one,4.07\nNC(=O)N(c1ccc(C(=O)N)c(n1)c2ccc(F)cc2F)c3c(F)cccc3F,\"InChI=1S/C19H12F4N4O2/c20-9-4-5-10(14(23)8-9)16-11(18(24)28)6-7-15(26-16)27(19(25)29)17-12(21)2-1-3-13(17)22/h1-8H,(H2,24,28)(H2,25,29)\",[N][C][=Branch1][C][=O][N][Branch2][Ring1][=C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=Branch1][Ring2][=N][Ring1][=Branch2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F],\"6-[carbamoyl-(2,6-difluorophenyl)amino]-2-(2,4-difluorophenyl)pyridine-3-carboxamide\",1.6\nCC[C@H]1[C@@H](Cc2cncn2C)COC1=O,\"InChI=1S/C11H16N2O2/c1-3-10-8(6-15-11(10)14)4-9-5-12-7-13(9)2/h5,7-8,10H,3-4,6H2,1-2H3/t8-,10-/m0/s1\",[C][C][C@H1][C@@H1][Branch1][#Branch2][C][C][=C][N][=C][N][Ring1][Branch1][C][C][O][C][Ring1][N][=O],\"(3s,4r)-3-ethyl-4-[(3-methylimidazol-4-yl)methyl]oxolan-2-one\",-0.37\nNC1=CC2=NNC(=O)N2c3cc(ccc13)c4ccc[nH]4,\"InChI=1S/C14H11N5O/c15-10-7-13-17-18-14(20)19(13)12-6-8(3-4-9(10)12)11-2-1-5-16-11/h1-7,16H,15H2,(H,18,20)\",[N][C][=C][C][=N][N][C][=Branch1][C][=O][N][Ring1][=Branch1][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=C][NH1][Ring1][Branch1],\"5-amino-8-(1h-pyrrol-2-yl)-2h-[1,2,4]triazolo[4,5-a]quinolin-1-one\",2.3\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3ccncc3)C(=O)C(F)(F)F,\"InChI=1S/C26H25F3N4O5/c1-16(2)22(23(35)26(27,28)29)32-21(34)14-33-20(18-6-4-3-5-7-18)9-8-19(24(33)36)31-25(37)38-15-17-10-12-30-13-11-17/h3-13,16,22H,14-15H2,1-2H3,(H,31,37)(H,32,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"pyridin-4-ylmethyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamate\",2.41\nCN1C(=O)C(=Cc2cnc(NC3CCOCC3)nc12)Oc4ccc(F)cc4F,\"InChI=1S/C19H18F2N4O3/c1-25-17-11(10-22-19(24-17)23-13-4-6-27-7-5-13)8-16(18(25)26)28-15-3-2-12(20)9-14(15)21/h2-3,8-10,13H,4-7H2,1H3,(H,22,23,24)\",[C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][Branch2][=C][C][=C][N][=C][Branch1][#Branch2][N][C][C][C][O][C][C][Ring1][=Branch1][N][=C][Ring2][Ring1][C][Ring1][=N][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F],\"6-(2,4-difluorophenoxy)-8-methyl-2-(oxan-4-ylamino)pyrido[6,5-d]pyrimidin-7-one\",2.76\nO=C1Oc2ccccc2C=C1c3ccccc3,InChI=1S/C15H10O2/c16-15-13(11-6-2-1-3-7-11)10-12-8-4-5-9-14(12)17-15/h1-10H,[O][=C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],3-phenylchromen-2-one,3.22\nCOc1ccccc1C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C19H25NO2/c1-22-17-5-3-2-4-16(17)18(21)20-12-19-9-13-6-14(10-19)8-15(7-13)11-19/h2-5,13-15H,6-12H2,1H3,(H,20,21)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-methoxybenzamide,4.43\nCS(=O)(=O)n1c2ccccc2c3cc(NC(=O)N4CCOCC4)ccc13,\"InChI=1S/C18H19N3O4S/c1-26(23,24)21-16-5-3-2-4-14(16)15-12-13(6-7-17(15)21)19-18(22)20-8-10-25-11-9-20/h2-7,12H,8-11H2,1H3,(H,19,22)\",[C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][=Branch1][Ring1][#C],n-(9-methylsulfonylcarbazol-3-yl)morpholine-4-carboxamide,2.7\nCC(C)(C)C(=O)Nc1ccc2c(c1)C(=O)C(=O)c3ccccc23,\"InChI=1S/C19H17NO3/c1-19(2,3)18(23)20-11-8-9-13-12-6-4-5-7-14(12)16(21)17(22)15(13)10-11/h4-10H,1-3H3,(H,20,23)\",[C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"n-(9,10-dioxophenanthren-2-yl)-2,2-dimethylpropanamide\",2.83\nCN1CCN(CC1)C(=O)OC2N(C(=O)c3nccnc23)c4ccc(Cl)cn4,\"InChI=1S/C17H17ClN6O3/c1-22-6-8-23(9-7-22)17(26)27-16-14-13(19-4-5-20-14)15(25)24(16)12-3-2-11(18)10-21-12/h2-5,10,16H,6-9H2,1H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][N][Branch1][#C][C][=Branch1][C][=O][C][=N][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=N][Ring1][#Branch1],\"[6-(5-chloropyridin-2-yl)-5-oxo-7h-pyrrolo[3,4-b]pyrazin-7-yl] 4-methylpiperazine-1-carboxylate\",1.1\nNc1ncnc2oc(c3cocc3)c(c4occc4)c12,\"InChI=1S/C14H9N3O3/c15-13-11-10(9-2-1-4-19-9)12(8-3-5-18-6-8)20-14(11)17-7-16-13/h1-7H,(H2,15,16,17)\",[N][C][=N][C][=N][C][O][C][Branch1][Branch2][C][=C][O][C][=C][Ring1][Branch1][=C][Branch1][Branch2][C][O][C][=C][C][=Ring1][Branch1][C][Ring2][Ring1][Ring1][=Ring1][#C],\"5-furan-2-yl-6-furan-3-ylfuro[3,2-e]pyrimidin-4-amine\",3.1\nOC(=O)c1ccc(Nc2ncc(Br)c(Nc3ccccc3)n2)cc1,\"InChI=1S/C17H13BrN4O2/c18-14-10-19-17(21-13-8-6-11(7-9-13)16(23)24)22-15(14)20-12-4-2-1-3-5-12/h1-10H,(H,23,24)(H2,19,20,21,22)\",[O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][Branch1][C][Br][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1],4-[[5-bromo-4-(phenylamino)pyrimidin-2-yl]amino]benzoic acid,1.65\nOc1ccc(O)c2C(=O)C=CC(=O)c12,\"InChI=1S/C10H6O4/c11-5-1-2-6(12)10-8(14)4-3-7(13)9(5)10/h1-4,11-12H\",[O][C][=C][C][=C][Branch1][C][O][C][C][=Branch1][C][=O][C][=C][C][=Branch1][C][=O][C][Ring1][=N][=Ring1][Branch2],\"5,8-dihydroxynaphthalene-1,4-dione\",1.91\nCC(=O)Nc1ccc(cc1)S(=O)(=O)Nc2ccccn2,\"InChI=1S/C13H13N3O3S/c1-10(17)15-11-5-7-12(8-6-11)20(18,19)16-13-4-2-3-9-14-13/h2-9H,1H3,(H,14,16)(H,15,17)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1],n-[4-(pyridin-2-ylsulfamoyl)phenyl]acetamide,0.24\nOc1ccc2C(=O)C(=COc2c1)c3ccc(O)c(O)c3,\"InChI=1S/C15H10O5/c16-9-2-3-10-14(6-9)20-7-11(15(10)19)8-1-4-12(17)13(18)5-8/h1-7,16-18H\",[O][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2],\"3-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one\",1.88\nCN1CCN(CC1)c2cc(Nc3cc(C)[nH]n3)nc(Sc4ccc(NC(=O)C5CC5)cc4)n2,\"InChI=1S/C23H28N8OS/c1-15-13-20(29-28-15)25-19-14-21(31-11-9-30(2)10-12-31)27-23(26-19)33-18-7-5-17(6-8-18)24-22(32)16-3-4-16/h5-8,13-14,16H,3-4,9-12H2,1-2H3,(H,24,32)(H2,25,26,27,28,29)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=N][C][Branch2][Ring1][=Branch1][S][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][C][C][C][Ring1][Ring1][C][=C][Ring1][N][=N][Ring2][Ring1][#Branch2],n-[4-[4-(4-methylpiperazin-1-yl)-6-[(5-methyl-1h-pyrazol-3-yl)amino]pyrimidin-2-yl]sulfanylphenyl]cyclopropanecarboxamide,3.47\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)Cc3ccc(cc3)C(=O)O)C(=O)C(F)(F)F,\"InChI=1S/C28H26F3N3O6/c1-16(2)24(25(37)28(29,30)31)33-23(36)15-34-21(18-6-4-3-5-7-18)13-12-20(26(34)38)32-22(35)14-17-8-10-19(11-9-17)27(39)40/h3-13,16,24H,14-15H2,1-2H3,(H,32,35)(H,33,36)(H,39,40)\",[C][C][Branch1][C][C][C][Branch2][Ring2][P][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"4-[2-oxo-2-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]amino]ethyl]benzoic acid\",0.35\nCc1nnc2CN=C(c3ccccc3Cl)c4cc(Cl)ccc4n12,\"InChI=1S/C17H12Cl2N4/c1-10-21-22-16-9-20-17(12-4-2-3-5-14(12)19)13-8-11(18)6-7-15(13)23(10)16/h2-8H,9H2,1H3\",[C][C][=N][N][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1],\"8-chloro-6-(2-chlorophenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine\",2.34\nC[C@@H]1CN(CC2(CC2)C(=O)N)CCN1S(=O)(=O)c3ccc(cc3)C(C)(O)C(F)(F)F,\"InChI=1S/C19H26F3N3O4S/c1-13-11-24(12-18(7-8-18)16(23)26)9-10-25(13)30(28,29)15-5-3-14(4-6-15)17(2,27)19(20,21)22/h3-6,13,27H,7-12H2,1-2H3,(H2,23,26)/t13-,17?/m1/s1\",[C][C@@H1][C][N][Branch1][=C][C][C][Branch1][Branch1][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][C][C][N][Ring1][=N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][O][C][Branch1][C][F][Branch1][C][F][F],\"1-[[(3r)-3-methyl-4-[4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenyl]sulfonylpiperazin-1-yl]methyl]cyclopropane-1-carboxamide\",1.03\nc1ccc2[nH]ncc2c1,\"InChI=1S/C7H6N2/c1-2-4-7-6(3-1)5-8-9-7/h1-5H,(H,8,9)\",[C][=C][C][=C][NH1][N][=C][C][Ring1][Branch1][=C][Ring1][=Branch2],1h-indazole,1.9\nCOc1ccc(OC(F)(F)F)cc1CN[C@H]2CCCN[C@H]2c3ccccc3,\"InChI=1S/C20H23F3N2O2/c1-26-18-10-9-16(27-20(21,22)23)12-15(18)13-25-17-8-5-11-24-19(17)14-6-3-2-4-7-14/h2-4,6-7,9-10,12,17,19,24-25H,5,8,11,13H2,1H3/t17-,19-/m0/s1\",[C][O][C][=C][C][=C][Branch1][#Branch2][O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][O][C][N][C@H1][C][C][C][N][C@H1][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(2s,3s)-n-[[2-methoxy-5-(trifluoromethoxy)phenyl]methyl]-2-phenylpiperidin-3-amine\",2.9\nNc1nc(cs1)c2ccc(Cl)cc2,\"InChI=1S/C9H7ClN2S/c10-7-3-1-6(2-4-7)8-5-13-9(11)12-8/h1-5H,(H2,11,12)\",[N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"4-(4-chlorophenyl)-1,3-thiazol-2-amine\",3.31\nNS(=O)(=O)c1cc(C(=O)O)c(NCc2occc2)cc1Cl,\"InChI=1S/C12H11ClN2O5S/c13-9-5-10(15-6-7-2-1-3-20-7)8(12(16)17)4-11(9)21(14,18)19/h1-5,15H,6H2,(H,16,17)(H2,14,18,19)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][=C][Branch1][#Branch2][N][C][C][O][C][=C][C][=Ring1][Branch1][C][=C][Ring1][S][Cl],4-chloro-2-(furan-2-ylmethylamino)-5-sulfamoylbenzoic acid,-0.9\nCCOC(=O)c1ccc(N)cc1,\"InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\",[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],ethyl 4-aminobenzoate,1.83\nCCc1c(C)nc2sc(C(=O)N)c(N)c2c1C,\"InChI=1S/C12H15N3OS/c1-4-7-5(2)8-9(13)10(11(14)16)17-12(8)15-6(7)3/h4,13H2,1-3H3,(H2,14,16)\",[C][C][C][=C][Branch1][C][C][N][=C][S][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][C][N][C][Ring1][=Branch2][=C][Ring1][=C][C],\"3-amino-5-ethyl-4,6-dimethylthieno[4,5-e]pyridine-2-carboxamide\",2.62\nOC(=O)c1ccc(OCC(=O)COc2ccc(SCCCCCc3ccccc3)cc2)cc1,\"InChI=1S/C27H28O5S/c28-23(19-31-24-12-10-22(11-13-24)27(29)30)20-32-25-14-16-26(17-15-25)33-18-6-2-5-9-21-7-3-1-4-8-21/h1,3-4,7-8,10-17H,2,5-6,9,18-20H2,(H,29,30)\",[O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][C][O][C][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][#C][S][C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=C],4-[2-oxo-3-[4-(5-phenylpentylsulfanyl)phenoxy]propoxy]benzoic acid,3.63\nOCCCN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C19H18ClN3O3S/c20-16-10-12-9-13(22-18(12)27-16)17(25)21-14-8-11-4-1-2-5-15(11)23(19(14)26)6-3-7-24/h1-2,4-5,9-10,14,22,24H,3,6-8H2,(H,21,25)\",[O][C][C][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-(3-hydroxypropyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.49\nCCCc1cc(cc(OC)c1OC)C2=N[C@H](CO2)C(=O)NO,\"InChI=1S/C15H20N2O5/c1-4-5-9-6-10(7-12(20-2)13(9)21-3)15-16-11(8-22-15)14(18)17-19/h6-7,11,19H,4-5,8H2,1-3H3,(H,17,18)/t11-/m1/s1\",[C][C][C][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=N][C@H1][Branch1][Branch1][C][O][Ring1][Branch1][C][=Branch1][C][=O][N][O],\"(4r)-2-(3,4-dimethoxy-5-propylphenyl)-n-hydroxy-4,5-dihydro-1,3-oxazole-4-carboxamide\",1.69\nON(C=O)C1(CS(=O)(=O)N2CCN(CC2)c3ccc(F)cc3)CCOCC1,\"InChI=1S/C17H24FN3O5S/c18-15-1-3-16(4-2-15)19-7-9-20(10-8-19)27(24,25)13-17(21(23)14-22)5-11-26-12-6-17/h1-4,14,23H,5-13H2\",[O][N][Branch1][Ring1][C][=O][C][Branch2][Ring1][=C][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][O][C][C][Ring2][Ring1][#Branch1],n-[4-[[4-(4-fluorophenyl)piperazin-1-yl]sulfonylmethyl]oxan-4-yl]-n-hydroxyformamide,0.85\nCOc1cc2ncc(C(=O)N)c(Nc3cc(C)ccc3F)c2cc1OC,\"InChI=1S/C19H18FN3O3/c1-10-4-5-13(20)15(6-10)23-18-11-7-16(25-2)17(26-3)8-14(11)22-9-12(18)19(21)24/h4-9H,1-3H3,(H2,21,24)(H,22,23)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C],\"4-[(2-fluoro-5-methylphenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",3.16\nCc1cc(NC(=O)c2ccc(Cl)cc2)n(n1)c3ccccc3,\"InChI=1S/C17H14ClN3O/c1-12-11-16(21(20-12)15-5-3-2-4-6-15)19-17(22)13-7-9-14(18)10-8-13/h2-11H,1H3,(H,19,22)\",[C][C][C][=C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Branch1][Ring2][N][=Ring1][#C][C][=C][C][=C][C][=C][Ring1][=Branch1],4-chloro-n-(5-methyl-2-phenylpyrazol-3-yl)benzamide,3.25\nCC1=C(CCC(=O)O)C(=O)Oc2cc(O)ccc12,\"InChI=1S/C13H12O5/c1-7-9-3-2-8(14)6-11(9)18-13(17)10(7)4-5-12(15)16/h2-3,6,14H,4-5H2,1H3,(H,15,16)\",[C][C][=C][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][P][Ring1][#Branch1],3-(7-hydroxy-4-methyl-2-oxochromen-3-yl)propanoic acid,-0.7\nCN(C)CC(O)COc1ccc(Nc2cc(Nc3ccc(F)cc3F)ncn2)cc1,\"InChI=1S/C21H23F2N5O2/c1-28(2)11-16(29)12-30-17-6-4-15(5-7-17)26-20-10-21(25-13-24-20)27-19-8-3-14(22)9-18(19)23/h3-10,13,16,29H,11-12H2,1-2H3,(H2,24,25,26,27)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][Branch1][=C][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][=N][C][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1],\"1-[4-[[6-[(2,4-difluorophenyl)amino]pyrimidin-4-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\",1.48\nCOc1cc2ncc(C(=O)N)c(Nc3ccccc3Cl)c2cc1OC,\"InChI=1S/C18H16ClN3O3/c1-24-15-7-10-14(8-16(15)25-2)21-9-11(18(20)23)17(10)22-13-6-4-3-5-12(13)19/h3-9H,1-2H3,(H2,20,23)(H,21,22)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C],\"4-[(2-chlorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",2.89\nC1CNCC(C1)c2nc3ccccc3s2,\"InChI=1S/C12H14N2S/c1-2-6-11-10(5-1)14-12(15-11)9-4-3-7-13-8-9/h1-2,5-6,9,13H,3-4,7-8H2\",[C][C][N][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2],\"2-piperidin-3-yl-1,3-benzothiazole\",1\n[O-][N+](=O)c1cccc2ccc(nc12)C(Cl)(Cl)Cl,\"InChI=1S/C10H5Cl3N2O2/c11-10(12,13)8-5-4-6-2-1-3-7(15(16)17)9(6)14-8/h1-5H\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Branch1][#Branch1][N][=C][Ring1][#Branch2][Ring1][=Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl],8-nitro-2-(trichloromethyl)quinoline,3.7\nCN(C)C(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C20H19ClN4O3S/c1-24(2)17(26)10-25-15-6-4-3-5-11(15)7-14(20(25)28)22-18(27)13-8-12-9-16(21)29-19(12)23-13/h3-6,8-9,14,23H,7,10H2,1-2H3,(H,22,27)\",[C][N][Branch1][C][C][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-(2-dimethylamino-2-oxoethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.07\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3ccncc3)C(=O)C(F)(F)F,\"InChI=1S/C26H26F3N5O4/c1-16(2)22(23(36)26(27,28)29)33-21(35)15-34-20(18-6-4-3-5-7-18)9-8-19(24(34)37)32-25(38)31-14-17-10-12-30-13-11-17/h3-13,16,22H,14-15H2,1-2H3,(H,33,35)(H2,31,32,38)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-6-phenyl-3-(pyridin-4-ylmethylcarbamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.16\nC[C@H](CO)Nc1nc(SCc2cccc(Cl)c2)nc3nc(N)sc13,\"InChI=1S/C15H16ClN5OS2/c1-8(6-22)18-12-11-13(19-14(17)24-11)21-15(20-12)23-7-9-3-2-4-10(16)5-9/h2-5,8,22H,6-7H2,1H3,(H3,17,18,19,20,21)/t8-/m1/s1\",[C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][=C][S][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1],\"(2r)-2-[[2-amino-5-[(3-chlorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\",3.31\nCCN1CCN(Cc2ccc(cc2)c3cc4c(N[C@H](C)c5ccccc5)ncnc4[nH]3)CC1,\"InChI=1S/C27H32N6/c1-3-32-13-15-33(16-14-32)18-21-9-11-23(12-10-21)25-17-24-26(28-19-29-27(24)31-25)30-20(2)22-7-5-4-6-8-22/h4-12,17,19-20H,3,13-16,18H2,1-2H3,(H2,28,29,30,31)/t20-/m1/s1\",[C][C][N][C][C][N][Branch2][Ring2][=Branch2][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][=C][N][C@H1][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][N][=C][Ring1][#C][NH1][Ring2][Ring1][C][C][C][Ring2][Ring1][#C],\"6-[4-[(4-ethylpiperazin-1-yl)methyl]phenyl]-n-[(1r)-1-phenylethyl]-7h-pyrrolo[3,2-e]pyrimidin-4-amine\",3.97\nOC(CN1CCOCC1)c2ccccc2,\"InChI=1S/C12H17NO2/c14-12(11-4-2-1-3-5-11)10-13-6-8-15-9-7-13/h1-5,12,14H,6-10H2\",[O][C][Branch1][#Branch2][C][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-morpholin-4-yl-1-phenylethanol,1\nOCCN1CCN(CCCN2c3ccccc3Sc4ccc(cc24)C(F)(F)F)CC1,\"InChI=1S/C22H26F3N3OS/c23-22(24,25)17-6-7-21-19(16-17)28(18-4-1-2-5-20(18)30-21)9-3-8-26-10-12-27(13-11-26)14-15-29/h1-2,4-7,16,29H,3,8-15H2\",[O][C][C][N][C][C][N][Branch2][Ring2][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][C][Ring2][Ring1][O],2-[4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]piperazin-1-yl]ethanol,3.8\nCN(C)c1cccc2c(cccc12)S(=O)(=O)N,\"InChI=1S/C12H14N2O2S/c1-14(2)11-7-3-6-10-9(11)5-4-8-12(10)17(13,15)16/h3-8H,1-2H3,(H2,13,15,16)\",[C][N][Branch1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N],5-dimethylaminonaphthalene-1-sulfonamide,1.95\nCc1[nH]c(C(=O)NC2CCN(CC2)c3nc(cs3)C(=O)O)c(Cl)c1Cl,\"InChI=1S/C15H16Cl2N4O3S/c1-7-10(16)11(17)12(18-7)13(22)19-8-2-4-21(5-3-8)15-20-9(6-25-15)14(23)24/h6,8,18H,2-5H2,1H3,(H,19,22)(H,23,24)\",[C][C][NH1][C][Branch2][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=Branch1][C][=O][O][=C][Branch1][C][Cl][C][=Ring2][Ring1][#Branch1][Cl],\"2-[4-[(3,4-dichloro-5-methyl1h-pyrrole-2-carbonyl)amino]piperidin-1-yl]-1,3-thiazole-4-carboxylic acid\",0.14\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)C(F)(F)F)C(=O)C(F)(F)F,\"InChI=1S/C20H19F6N3O5S/c1-11(2)16(17(31)19(21,22)23)27-15(30)10-29-14(12-6-4-3-5-7-12)9-8-13(18(29)32)28-35(33,34)20(24,25)26/h3-9,11,16,28H,10H2,1-2H3,(H,27,30)\",[C][C][Branch1][C][C][C][Branch2][Ring2][N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-6-phenyl-3-(trifluoromethylsulfonylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.01\nFc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3ccc(F)cc3,\"InChI=1S/C19H17F2NO2/c20-16-5-1-13(2-6-16)18(23)14-9-11-22(12-10-14)19(24)15-3-7-17(21)8-4-15/h1-8,14H,9-12H2\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],[1-(4-fluorobenzoyl)piperidin-4-yl]-(4-fluorophenyl)methanone,2.9\nCC(C(=O)O)c1cccc(c1)C(=O)c2ccccc2,\"InChI=1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)\",[C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[3-(benzoyl)phenyl]propanoic acid,-0.12\nNc1nccc(\\C=C\\c2ccc(Cl)cc2)n1,\"InChI=1S/C12H10ClN3/c13-10-4-1-9(2-5-10)3-6-11-7-8-15-12(14)16-11/h1-8H,(H2,14,15,16)/b6-3+\",[N][C][=N][C][=C][C][Branch1][=C][\\C][=C][\\C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][#C],4-[(e)-2-(4-chlorophenyl)ethenyl]pyrimidin-2-amine,3.5\nCCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)C)C=O,\"InChI=1S/C20H37N3O4/c1-7-8-9-16(12-24)22-19(26)18(11-14(4)5)23-20(27)17(10-13(2)3)21-15(6)25/h12-14,16-18H,7-11H2,1-6H3,(H,21,25)(H,22,26)(H,23,27)/t16-,17-,18-/m0/s1\",[C][C][C][C][C@H1][Branch2][Ring2][Ring1][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][C][C][=O],(2s)-2-[[(2s)-2-acetamido-4-methylpentanoyl]amino]-4-methyl-n-[(2s)-1-oxohexan-2-yl]pentanamide,2.6\nOC(=O)c1cccnc1Nc2cccc(c2)C(F)(F)F,\"InChI=1S/C13H9F3N2O2/c14-13(15,16)8-3-1-4-9(7-8)18-11-10(12(19)20)5-2-6-17-11/h1-7H,(H,17,18)(H,19,20)\",[O][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],2-[[3-(trifluoromethyl)phenyl]amino]pyridine-3-carboxylic acid,1\nCn1cnc(c1Sc2ncnc3nc[nH]c23)[N+](=O)[O-],\"InChI=1S/C9H7N7O2S/c1-15-4-14-7(16(17)18)9(15)19-8-5-6(11-2-10-5)12-3-13-8/h2-4H,1H3,(H,10,11,12,13)\",[C][N][C][=N][C][=Branch2][Ring1][C][=C][Ring1][Branch1][S][C][=N][C][=N][C][N][=C][NH1][C][Ring1][=Branch2][=Ring1][Branch1][N+1][=Branch1][C][=O][O-1],6-(3-methyl-5-nitroimidazol-4-yl)sulfanyl-7h-purine,0.19\nO[C@@H](CNCCc1ccc(NC[C@H](O)c2ccccc2)cc1)c3ccc(O)c(NC=O)c3,\"InChI=1S/C25H29N3O4/c29-17-28-22-14-20(8-11-23(22)30)24(31)15-26-13-12-18-6-9-21(10-7-18)27-16-25(32)19-4-2-1-3-5-19/h1-11,14,17,24-27,30-32H,12-13,15-16H2,(H,28,29)/t24-,25-/m0/s1\",[O][C@@H1][Branch2][Ring1][=N][C][N][C][C][C][=C][C][=C][Branch1][#C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=C][Branch1][C][O][C][Branch1][Ring2][N][C][=O][=C][Ring1][#Branch2],n-[2-hydroxy-5-[(1r)-1-hydroxy-2-[2-[4-[[(2r)-2-hydroxy-2-phenylethyl]amino]phenyl]ethylamino]ethyl]phenyl]formamide,0.02\nCCCC1CCCCC(=N1)N,\"InChI=1S/C9H18N2/c1-2-5-8-6-3-4-7-9(10)11-8/h8H,2-7H2,1H3,(H2,10,11)\",[C][C][C][C][C][C][C][C][C][=Branch1][Ring2][=N][Ring1][#Branch1][N],\"7-propyl-4,5,6,7-tetrahydro-3h-azepin-2-amine\",1.1\nNNC1=Nc2ccccc2NC1=O,\"InChI=1S/C8H8N4O/c9-12-7-8(13)11-6-4-2-1-3-5(6)10-7/h1-4H,9H2,(H,10,12)(H,11,13)\",[N][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring1][#Branch2][=O],3-hydrazinyl-1h-quinoxalin-2-one,0.44\nClc1c(NCC2CCNCC2)nccc1C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C23H33ClN4O/c24-20-19(3-6-26-21(20)27-13-15-1-4-25-5-2-15)22(29)28-14-23-10-16-7-17(11-23)9-18(8-16)12-23/h3,6,15-18,25H,1-2,4-5,7-14H2,(H,26,27)(H,28,29)\",[Cl][C][=C][Branch1][O][N][C][C][C][C][N][C][C][Ring1][=Branch1][N][=C][C][=C][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-3-chloro-2-(piperidin-4-ylmethylamino)pyridine-4-carboxamide,0.6\nCOCCOC(=O)C1=C(C)NC(=C(C1c2cccc(c2)[N+](=O)[O-])C(=O)OC(C)C)C,\"InChI=1S/C21H26N2O7/c1-12(2)30-21(25)18-14(4)22-13(3)17(20(24)29-10-9-28-5)19(18)15-7-6-8-16(11-15)23(26)27/h6-8,11-12,19,22H,9-10H2,1-5H3\",[C][O][C][C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][C][=Branch2][Ring1][P][=C][Branch2][Ring1][Ring1][C][Ring1][#Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][=Branch1][C][=O][O][C][Branch1][C][C][C][C],\"o5-(2-methoxyethyl) o3-propan-2-yl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate\",3.8\nCCN1C(=O)C2=C(OC(=CC2=O)O)c3ccccc13,\"InChI=1S/C14H11NO4/c1-2-15-9-6-4-3-5-8(9)13-12(14(15)18)10(16)7-11(17)19-13/h3-7,17H,2H2,1H3\",[C][C][N][C][=Branch1][C][=O][C][=C][Branch1][O][O][C][=Branch1][=Branch1][=C][C][Ring1][=Branch1][=O][O][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1],\"6-ethyl-2-hydroxypyrano[3,2-c]quinoline-4,5-dione\",1.13\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(cccc34)S(=O)(=O)C,\"InChI=1S/C22H20N2O4S/c1-13-7-8-18-17(11-13)21(14(2)24(18)12-20(25)26)15-9-10-23-22-16(15)5-4-6-19(22)29(3,27)28/h4-11H,12H2,1-3H3,(H,25,26)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],\"2-[2,5-dimethyl-3-(8-methylsulfonylquinolin-4-yl)indol-1-yl]acetic acid\",-0.34\nCCOC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)c2cccc3ccccc23,\"InChI=1S/C22H21NO4/c1-2-27-22(26)20(14-15-10-12-17(24)13-11-15)23-21(25)19-9-5-7-16-6-3-4-8-18(16)19/h3-13,20,24H,2,14H2,1H3,(H,23,25)/t20-/m0/s1\",[C][C][O][C][=Branch1][C][=O][C@H1][Branch1][=N][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],ethyl (2s)-3-(4-hydroxyphenyl)-2-(naphthalene-1-carbonylamino)propanoate,3.12\nNCCCCN(Cc1nc2ccccc2[nH]1)C3CCCc4cccnc34,\"InChI=1S/C21H27N5/c22-12-3-4-14-26(15-20-24-17-9-1-2-10-18(17)25-20)19-11-5-7-16-8-6-13-23-21(16)19/h1-2,6,8-10,13,19H,3-5,7,11-12,14-15,22H2,(H,24,25)\",[N][C][C][C][C][N][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][C][C][C][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1],\"n-(1h-benzimidazol-2-ylmethyl)-n-(5,6,7,8-tetrahydroquinolin-8-yl)butane-1,4-diamine\",0.83\nCC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3CCN(CC3)c4cnccn4)c(F)c2,\"InChI=1S/C20H23FN6O3/c1-14(28)24-11-16-13-27(20(29)30-16)15-2-3-18(17(21)10-15)25-6-8-26(9-7-25)19-12-22-4-5-23-19/h2-5,10,12,16H,6-9,11,13H2,1H3,(H,24,28)/t16-/m0/s1\",[C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][Ring1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][N][=C][C][=N][Ring1][=Branch1][C][Branch1][C][F][=C][Ring2][Ring1][Ring1],\"n-[[(5s)-3-[3-fluoro-4-(4-pyrazin-2-ylpiperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\",1.49\nCCN(CC)CCOCCOC(=O)C1(CCCC1)c2ccccc2,\"InChI=1S/C20H31NO3/c1-3-21(4-2)14-15-23-16-17-24-19(22)20(12-8-9-13-20)18-10-6-5-7-11-18/h5-7,10-11H,3-4,8-9,12-17H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][C][O][C][C][O][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(2-diethylaminoethoxy)ethyl 1-phenylcyclopentane-1-carboxylate,1.33\nFc1ccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)cc1F,\"InChI=1S/C18H16F2N6O3/c19-13-3-1-11(9-14(13)20)23-18-25-24-17(29-18)16(27)22-12-2-4-15(21-10-12)26-5-7-28-8-6-26/h1-4,9-10H,5-8H2,(H,22,27)(H,23,25)\",[F][C][=C][C][=C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][O][F],\"5-[(3,4-difluorophenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\",2.9\nCc1c(Sc2ccc(Cl)cc2)c3cc(ccc3n1CC(=O)O)c4ccccc4,\"InChI=1S/C23H18ClNO2S/c1-15-23(28-19-10-8-18(24)9-11-19)20-13-17(16-5-3-2-4-6-16)7-12-21(20)25(15)14-22(26)27/h2-13H,14H2,1H3,(H,26,27)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[3-(4-chlorophenyl)sulfanyl-2-methyl-5-phenylindol-1-yl]acetic acid,3.7\nFC(F)(F)c1cc(COCC(N2CCNCC2)c3ccccc3)cc(c1)C(F)(F)F,\"InChI=1S/C21H22F6N2O/c22-20(23,24)17-10-15(11-18(12-17)21(25,26)27)13-30-14-19(16-4-2-1-3-5-16)29-8-6-28-7-9-29/h1-5,10-12,19,28H,6-9,13-14H2\",[F][C][Branch1][C][F][Branch1][C][F][C][=C][C][Branch2][Ring1][#Branch1][C][O][C][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"1-[2-[[3,5-bis(trifluoromethyl)phenyl]methoxy]-1-phenylethyl]piperazine\",2.9\nCN1C(=O)N(CCCCC(=O)C)C(=O)c2c1ncn2C,\"InChI=1S/C13H18N4O3/c1-9(18)6-4-5-7-17-12(19)10-11(14-8-15(10)2)16(3)13(17)20/h8H,4-7H2,1-3H3\",[C][N][C][=Branch1][C][=O][N][Branch1][#Branch2][C][C][C][C][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][=C][Ring1][#C][N][=C][N][Ring1][Branch1][C],\"3,7-dimethyl-1-(5-oxohexyl)purine-2,6-dione\",0.22\nC[C@H]1CN(Cc2cc(Cl)ccc2CC(=O)O)CCN1S(=O)(=O)Cc3ccccc3,\"InChI=1S/C21H25ClN2O4S/c1-16-13-23(14-19-11-20(22)8-7-18(19)12-21(25)26)9-10-24(16)29(27,28)15-17-5-3-2-4-6-17/h2-8,11,16H,9-10,12-15H2,1H3,(H,25,26)/t16-/m0/s1\",[C][C@H1][C][N][Branch2][Ring1][Ring1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-chloro-2-[[(3s)-3-methyl-4-(phenylmethylsulfonyl)piperazin-1-yl]methyl]phenyl]acetic acid,1.12\nC(Nc1nc2ccccc2[nH]1)c3ccccc3,\"InChI=1S/C14H13N3/c1-2-6-11(7-3-1)10-15-14-16-12-8-4-5-9-13(12)17-14/h1-9H,10H2,(H2,15,16,17)\",[C][Branch1][#C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],n-(phenylmethyl)-1h-benzimidazol-2-amine,2.76\nOCCOCCN1CCN(CC1)C(c2ccccc2)c3ccc(Cl)cc3,\"InChI=1S/C21H27ClN2O2/c22-20-8-6-19(7-9-20)21(18-4-2-1-3-5-18)24-12-10-23(11-13-24)14-16-26-17-15-25/h1-9,21,25H,10-17H2\",[O][C][C][O][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[2-[4-[(4-chlorophenyl)-phenylmethyl]piperazin-1-yl]ethoxy]ethanol,3.08\nCOc1ccc(CN(CCN(C)C)c2ccccn2)cc1,\"InChI=1S/C17H23N3O/c1-19(2)12-13-20(17-6-4-5-11-18-17)14-15-7-9-16(21-3)10-8-15/h4-11H,12-14H2,1-3H3\",[C][O][C][=C][C][=C][Branch2][Ring1][Ring2][C][N][Branch1][Branch2][C][C][N][Branch1][C][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1],\"n-[(4-methoxyphenyl)methyl]-n',n'-dimethyl-n-pyridin-2-ylethane-1,2-diamine\",1.39\nOC[C@H]1CCCN1CCCOc2ccc3c(Nc4cc(CC(=O)Nc5cccc(F)c5F)[nH]n4)ncnc3c2,\"InChI=1S/C27H29F2N7O3/c28-21-5-1-6-22(26(21)29)32-25(38)13-17-12-24(35-34-17)33-27-20-8-7-19(14-23(20)30-16-31-27)39-11-3-10-36-9-2-4-18(36)15-37/h1,5-8,12,14,16,18,37H,2-4,9-11,13,15H2,(H,32,38)(H2,30,31,33,34,35)/t18-/m1/s1\",[O][C][C@H1][C][C][C][N][Ring1][Branch1][C][C][C][O][C][=C][C][=C][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=N][C][=N][C][Ring2][Ring1][Branch2][=C][Ring2][Ring1][N],\"n-(2,3-difluorophenyl)-2-[5-[[7-[3-[(2r)-2-(hydroxymethyl)pyrrolidin-1-yl]propoxy]quinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\",2.06\nNC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C18H15ClN4O3S/c19-14-7-10-6-11(22-17(10)27-14)16(25)21-12-5-9-3-1-2-4-13(9)23(18(12)26)8-15(20)24/h1-4,6-7,12,22H,5,8H2,(H2,20,24)(H,21,25)\",[N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"n-[1-(2-amino-2-oxoethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-2-chloro-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.22\nCN(C)CCNC(=O)c1c(C)[nH]c(\\C=C\\2/C(=O)Nc3ccc(F)cc23)c1C,\"InChI=1S/C20H23FN4O2/c1-11-17(23-12(2)18(11)20(27)22-7-8-25(3)4)10-15-14-9-13(21)5-6-16(14)24-19(15)26/h5-6,9-10,23H,7-8H2,1-4H3,(H,22,27)(H,24,26)/b15-10-\",[C][N][Branch1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][NH1][C][Branch2][Ring1][Branch1][\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][\\-Ring1][O][Ring1][#Branch1][=C][Ring2][Ring1][C][C],\"n-(2-dimethylaminoethyl)-5-[(z)-(5-fluoro-2-oxo-1h-indol-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide\",1.75\nFc1ccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)cc1,\"InChI=1S/C18H17FN6O3/c19-12-1-3-13(4-2-12)22-18-24-23-17(28-18)16(26)21-14-5-6-15(20-11-14)25-7-9-27-10-8-25/h1-6,11H,7-10H2,(H,21,26)(H,22,24)\",[F][C][=C][C][=C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][O],\"5-[(4-fluorophenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\",3\nCN([C@H]1CC[C@@]2(CCCO2)C[C@@H]1N3CCCC3)C(=O)Cc4ccccc4,\"InChI=1S/C22H32N2O2/c1-23(21(25)16-18-8-3-2-4-9-18)19-10-12-22(11-7-15-26-22)17-20(19)24-13-5-6-14-24/h2-4,8-9,19-20H,5-7,10-17H2,1H3/t19-,20-,22-/m0/s1\",[C][N][Branch2][Ring1][Branch2][C@H1][C][C][C@@][Branch1][#Branch1][C][C][C][O][Ring1][Branch1][C][C@@H1][Ring1][#Branch2][N][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-methyl-2-phenyl-n-[(5r,7s,8s)-7-pyrrolidin-1-yl-1-oxaspiro[4.5]decan-8-yl]acetamide\",0.99\nCOc1ccc(cc1)C(=O)Nc2cc(NC(=O)c3cccc(c3)N(C)C)ccc2C,\"InChI=1S/C24H25N3O3/c1-16-8-11-19(25-24(29)18-6-5-7-20(14-18)27(2)3)15-22(16)26-23(28)17-9-12-21(30-4)13-10-17/h5-15H,1-4H3,(H,25,29)(H,26,28)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][C][C],3-dimethylamino-n-[3-[(4-methoxybenzoyl)amino]-4-methylphenyl]benzamide,3.17\nC[C@H]([C@H](O)c1ccc(O)cc1)N2CCC(O)(CC2)c3ccccc3,\"InChI=1S/C20H25NO3/c1-15(19(23)16-7-9-18(22)10-8-16)21-13-11-20(24,12-14-21)17-5-3-2-4-6-17/h2-10,15,19,22-24H,11-14H2,1H3/t15-,19+/m1/s1\",[C][C@H1][Branch1][S][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][N][C][C][C][Branch1][C][O][Branch1][Branch1][C][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-[(1r,2r)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]-4-phenylpiperidin-4-ol\",0.91\nNC(=O)Nc1sc(cc1C(=O)N[C@H]2CCCNC2)c3ccc(F)cc3,\"InChI=1S/C17H19FN4O2S/c18-11-5-3-10(4-6-11)14-8-13(16(25-14)22-17(19)24)15(23)21-12-2-1-7-20-9-12/h3-6,8,12,20H,1-2,7,9H2,(H,21,23)(H3,19,22,24)/t12-/m0/s1\",[N][C][=Branch1][C][=O][N][C][S][C][=Branch2][Ring1][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],2-(carbamoylamino)-5-(4-fluorophenyl)-n-[(3s)-piperidin-3-yl]thiophene-3-carboxamide,1.76\nOc1ccc(cc1)C(c2ccc(O)cc2)C(Cl)(Cl)Cl,\"InChI=1S/C14H11Cl3O2/c15-14(16,17)13(9-1-5-11(18)6-2-9)10-3-7-12(19)8-4-10/h1-8,13,18-19H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl],\"4-[2,2,2-trichloro-1-(4-hydroxyphenyl)ethyl]phenol\",3.86\nCSc1ccc(OCc2ccccc2)c(\\C=C\\c3ccc(cn3)C(=O)O)c1,\"InChI=1S/C22H19NO3S/c1-27-20-11-12-21(26-15-16-5-3-2-4-6-16)17(13-20)7-9-19-10-8-18(14-23-19)22(24)25/h2-14H,15H2,1H3,(H,24,25)/b9-7+\",[C][S][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch2][Ring1][C][\\C][=C][\\C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O][=C][Ring2][Ring1][=Branch2],6-[(e)-2-[5-methylsulfanyl-2-(phenylmethoxy)phenyl]ethenyl]pyridine-3-carboxylic acid,2.45\nC1CN=C(N1)c2ccc3ccccc3n2,\"InChI=1S/C12H11N3/c1-2-4-10-9(3-1)5-6-11(15-10)12-13-7-8-14-12/h1-6H,7-8H2,(H,13,14)\",[C][C][N][=C][Branch1][Ring2][N][Ring1][Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"2-(4,5-dihydro-1h-imidazol-2-yl)quinoline\",0.6\nCC1=CC(=O)Oc2cc3NCCCc3cc12,\"InChI=1S/C13H13NO2/c1-8-5-13(15)16-12-7-11-9(6-10(8)12)3-2-4-14-11/h5-7,14H,2-4H2,1H3\",[C][C][=C][C][=Branch1][C][=O][O][C][=C][C][N][C][C][C][C][=Ring1][=Branch1][C][=C][Ring1][#C][Ring1][#Branch2],\"4-methyl-6,7,8,9-tetrahydropyrano[5,6-g]quinolin-2-one\",2.7\nO[C@@H](CNCCCSCCOCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H28N2O4S2/c25-18-8-7-17(21-20(18)24-22(27)30-21)19(26)15-23-10-4-13-29-14-12-28-11-9-16-5-2-1-3-6-16/h1-3,5-8,19,23,25-26H,4,9-15H2,(H,24,27)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][C][S][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-phenylethoxy)ethylsulfanyl]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\",2.3\nCC1=C(CCC(=O)O)C(=O)Oc2c(C)c(O)ccc12,\"InChI=1S/C14H14O5/c1-7-9-3-5-11(15)8(2)13(9)19-14(18)10(7)4-6-12(16)17/h3,5,15H,4,6H2,1-2H3,(H,16,17)\",[C][C][=C][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][C][=Branch1][C][=O][O][C][=C][Branch1][C][C][C][Branch1][C][O][=C][C][=C][Ring2][Ring1][C][Ring1][Branch2],\"3-(7-hydroxy-4,8-dimethyl-2-oxochromen-3-yl)propanoic acid\",-0.3\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)NCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C26H27F3N4O5S/c1-17(2)23(24(35)26(27,28)29)31-22(34)16-33-21(19-11-7-4-8-12-19)14-13-20(25(33)36)32-39(37,38)30-15-18-9-5-3-6-10-18/h3-14,17,23,30,32H,15-16H2,1-2H3,(H,31,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-6-phenyl-3-(phenylmethylsulfamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.57\nCc1c(CC(=O)O)c2cc(F)ccc2n1S(=O)(=O)c3ccc(cc3)S(=O)(=O)C,\"InChI=1S/C18H16FNO6S2/c1-11-15(10-18(21)22)16-9-12(19)3-8-17(16)20(11)28(25,26)14-6-4-13(5-7-14)27(2,23)24/h3-9H,10H2,1-2H3,(H,21,22)\",[C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][N][Ring1][=C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],2-[5-fluoro-2-methyl-1-(4-methylsulfonylphenyl)sulfonylindol-3-yl]acetic acid,-0.44\nCCCN(CCC)CCc1cccc2NC(=O)Cc12,\"InChI=1S/C16H24N2O/c1-3-9-18(10-4-2)11-8-13-6-5-7-15-14(13)12-16(19)17-15/h5-7H,3-4,8-12H2,1-2H3,(H,17,19)\",[C][C][C][N][Branch1][Ring2][C][C][C][C][C][C][=C][C][=C][C][N][C][=Branch1][C][=O][C][C][Ring1][#Branch2][=Ring1][=Branch1],\"4-[2-(dipropylamino)ethyl]-1,3-dihydroindol-2-one\",0.76\nClc1ccc(cc1C(=O)NCCc2ccccc2)N3N=CC(=O)NC3=O,\"InChI=1S/C18H15ClN4O3/c19-15-7-6-13(23-18(26)22-16(24)11-21-23)10-14(15)17(25)20-9-8-12-4-2-1-3-5-12/h1-7,10-11H,8-9H2,(H,20,25)(H,22,24,26)\",[Cl][C][=C][C][=C][Branch2][Ring1][Ring2][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O],\"2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)-n-(2-phenylethyl)benzamide\",0.74\nCc1ccc2c(c1)c([S+]([O-])c3ccc(Cl)cc3)c(C)n2CC(=O)O,\"InChI=1S/C18H16ClNO3S/c1-11-3-8-16-15(9-11)18(12(2)20(16)10-17(21)22)24(23)14-6-4-13(19)5-7-14/h3-9H,10H2,1-2H3,(H,21,22)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][S][S+1][Branch1][C][O-1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][S][C][C][=Branch1][C][=O][O],\"2-[3-(4-chlorophenyl)sulfinyl-2,5-dimethylindol-1-yl]acetic acid\",0.05\nCCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3ccc(Cl)c(Cl)c3,\"InChI=1S/C23H26Cl2N2O/c1-3-27(4-2)23(28)18-7-5-16(6-8-18)22(17-11-13-26-14-12-17)19-9-10-20(24)21(25)15-19/h5-10,15,26H,3-4,11-14H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"4-[(3,4-dichlorophenyl)-piperidin-4-ylidenemethyl]-n,n-diethylbenzamide\",2.4\nCNc1ncc(s1)C(=O)c2ccccc2,\"InChI=1S/C11H10N2OS/c1-12-11-13-7-9(15-11)10(14)8-5-3-2-4-6-8/h2-7H,1H3,(H,12,13)\",[C][N][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(2-methylamino-1,3-thiazol-5-yl)-phenylmethanone\",2.36\nCOc1cc2ncnc(Nc3ccccc3)c2cc1OC,\"InChI=1S/C16H15N3O2/c1-20-14-8-12-13(9-15(14)21-2)17-10-18-16(12)19-11-6-4-3-5-7-11/h3-10H,1-2H3,(H,17,18,19)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][Ring1][P][O][C],\"6,7-dimethoxy-n-phenylquinazolin-4-amine\",3.04\nCN1CCN(CC1)c2ccc(Nc3ccnc4ccccc34)cc2,\"InChI=1S/C20H22N4/c1-23-12-14-24(15-13-23)17-8-6-16(7-9-17)22-20-10-11-21-19-5-3-2-4-18(19)20/h2-11H,12-15H2,1H3,(H,21,22)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][S][N][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring1][P],n-[4-(4-methylpiperazin-1-yl)phenyl]quinolin-4-amine,1.3\nCNC[C@H](O)c1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C21H29ClN2O2/c1-23-11-19(25)16-2-3-18(22)17(7-16)20(26)24-12-21-8-13-4-14(9-21)6-15(5-13)10-21/h2-3,7,13-15,19,23,25H,4-6,8-12H2,1H3,(H,24,26)/t13?,14?,15?,19-,21?/m0/s1\",[C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chloro-5-[(1r)-1-hydroxy-2-methylaminoethyl]benzamide,1.41\nOC(CCN1CCCCC1)(C2CC3CC2C=C3)c4ccccc4,\"InChI=1S/C21H29NO/c23-21(19-7-3-1-4-8-19,11-14-22-12-5-2-6-13-22)20-16-17-9-10-18(20)15-17/h1,3-4,7-10,17-18,20,23H,2,5-6,11-16H2\",[O][C][Branch1][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][Branch1][N][C][C][C][C][C][Ring1][Branch1][C][=C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],1-(6-bicyclo[2.2.1]hept-2-enyl)-1-phenyl-3-piperidin-1-ylpropan-1-ol,2.49\nCOc1ccc(CNC(=O)CSc2nc3cccnc3s2)cc1,\"InChI=1S/C16H15N3O2S2/c1-21-12-6-4-11(5-7-12)9-18-14(20)10-22-16-19-13-3-2-8-17-15(13)23-16/h2-8H,9-10H2,1H3,(H,18,20)\",[C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][S][C][=N][C][=C][C][=C][N][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][Ring2][Ring1][Branch1],\"n-[(4-methoxyphenyl)methyl]-2-([1,3]thiazolo[5,4-b]pyridin-2-ylsulfanyl)acetamide\",2.5\nC[C@@H](NC(=O)C)c1ccc(Nc2ncc3cc(ccc3n2)c4ccncc4)cc1,\"InChI=1S/C23H21N5O/c1-15(26-16(2)29)17-3-6-21(7-4-17)27-23-25-14-20-13-19(5-8-22(20)28-23)18-9-11-24-12-10-18/h3-15H,1-2H3,(H,26,29)(H,25,27,28)/t15-/m1/s1\",[C][C@@H1][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][=N][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1],n-[(1r)-1-[4-[(6-pyridin-4-ylquinazolin-2-yl)amino]phenyl]ethyl]acetamide,3.18\nCCCc1c(O)c(O)c(C(=O)O)c2cc(Cc3ccccc3)c(C)cc12,\"InChI=1S/C22H22O4/c1-3-7-16-17-10-13(2)15(11-14-8-5-4-6-9-14)12-18(17)19(22(25)26)21(24)20(16)23/h4-6,8-10,12,23-24H,3,7,11H2,1-2H3,(H,25,26)\",[C][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][Ring2][Ring1][#Branch1][Ring1][=C],\"2,3-dihydroxy-6-methyl-7-(phenylmethyl)-4-propylnaphthalene-1-carboxylic acid\",2.6\nCOc1cnc(nc1N(C)c2ccccc2)c3ccccn3,\"InChI=1S/C17H16N4O/c1-21(13-8-4-3-5-9-13)17-15(22-2)12-19-16(20-17)14-10-6-7-11-18-14/h3-12H,1-2H3\",[C][O][C][=C][N][=C][Branch1][P][N][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1],5-methoxy-n-methyl-n-phenyl-2-pyridin-2-ylpyrimidin-4-amine,2.79\nCS(=O)(=O)c1ccc(cc1Cl)[C@@H](C[C@H]2CCC(=O)C2)C(=O)Nc3cnccn3,\"InChI=1S/C19H20ClN3O4S/c1-28(26,27)17-5-3-13(10-16(17)20)15(9-12-2-4-14(24)8-12)19(25)23-18-11-21-6-7-22-18/h3,5-7,10-12,15H,2,4,8-9H2,1H3,(H,22,23,25)/t12-,15+/m0/s1\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C@@H1][Branch1][N][C][C@H1][C][C][C][=Branch1][C][=O][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][N][=C][C][=N][Ring1][=Branch1],(2r)-2-(3-chloro-4-methylsulfonylphenyl)-3-[(1r)-3-oxocyclopentyl]-n-pyrazin-2-ylpropanamide,1.39\nCN(C(=O)N1CCC(CC1)N2CCC(CC2)Oc3ccc(Cl)c(Cl)c3)S(=O)(=O)c4ccc(C)cc4,\"InChI=1S/C25H31Cl2N3O4S/c1-18-3-6-22(7-4-18)35(32,33)28(2)25(31)30-13-9-19(10-14-30)29-15-11-20(12-16-29)34-21-5-8-23(26)24(27)17-21/h3-8,17,19-20H,9-16H2,1-2H3\",[C][N][Branch2][Ring2][Branch2][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-methyl-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\",4.49\nCc1ccnc(NCc2ccccc2)c1,\"InChI=1S/C13H14N2/c1-11-7-8-14-13(9-11)15-10-12-5-3-2-4-6-12/h2-9H,10H2,1H3,(H,14,15)\",[C][C][=C][C][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C],4-methyl-n-(phenylmethyl)pyridin-2-amine,3.08\nCN1C=CNC1=S,\"InChI=1S/C4H6N2S/c1-6-3-2-5-4(6)7/h2-3H,1H3,(H,5,7)\",[C][N][C][=C][N][C][Ring1][Branch1][=S],1-methyl-3h-imidazole-2-thione,-0.42\nCOc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN4CCC[C@@H]4C(=O)N,\"InChI=1S/C21H21ClFN5O2/c1-30-18-9-16-13(8-12(18)10-28-7-3-6-17(28)20(24)29)21(26-11-25-16)27-15-5-2-4-14(22)19(15)23/h2,4-5,8-9,11,17H,3,6-7,10H2,1H3,(H2,24,29)(H,25,26,27)/t17-/m1/s1\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][C][C][C][C@@H1][Ring1][Branch1][C][=Branch1][C][=O][N],(2r)-1-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl]pyrrolidine-2-carboxamide,3.58\nCCN(C1CCN(CCC(C2CCN(Cc3ccccc3)CC2)c4ccccc4)CC1)C(=O)Cc5ccc(cc5)S(=O)(=O)C,\"InChI=1S/C37H49N3O3S/c1-3-40(37(41)28-30-14-16-35(17-15-30)44(2,42)43)34-20-25-38(26-21-34)27-22-36(32-12-8-5-9-13-32)33-18-23-39(24-19-33)29-31-10-6-4-7-11-31/h4-17,33-34,36H,3,18-29H2,1-2H3\",[C][C][N][Branch2][Ring2][=C][C][C][C][N][Branch2][Ring2][C][C][C][C][Branch2][Ring1][Ring2][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring1][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[3-phenyl-3-[1-(phenylmethyl)piperidin-4-yl]propyl]piperidin-4-yl]acetamide,2.41\nClc1cccc(c1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C23H26Cl3N3O4S/c24-16-2-1-3-20(14-16)34(31,32)27-23(30)29-10-6-17(7-11-29)28-12-8-18(9-13-28)33-19-4-5-21(25)22(26)15-19/h1-5,14-15,17-18H,6-13H2,(H,27,30)\",[Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"n-(3-chlorophenyl)sulfonyl-4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidine-1-carboxamide\",2.62\nOc1ccc(cc1)C2=Cc3cc(O)ccc3OC2=O,\"InChI=1S/C15H10O4/c16-11-3-1-9(2-4-11)13-8-10-7-12(17)5-6-14(10)19-15(13)18/h1-8,16-17H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O],6-hydroxy-3-(4-hydroxyphenyl)chromen-2-one,2.9\nCN1C(=O)CN=C(c2ccccc2F)c3cc(ccc13)[N+](=O)[O-],\"InChI=1S/C16H12FN3O3/c1-19-14-7-6-10(20(22)23)8-12(14)16(18-9-15(19)21)11-4-2-3-5-13(11)17/h2-8H,9H2,1H3\",[C][N][C][=Branch1][C][=O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1],\"5-(2-fluorophenyl)-1-methyl-7-nitro-3h-1,4-benzodiazepin-2-one\",2.1\nCCN1CCN(CC(=O)Nc2ccc(c3cccc4C(=O)C=C(Oc34)N5CCOCC5)c6sc7ccccc7c26)CC1,\"InChI=1S/C33H34N4O4S/c1-2-35-12-14-36(15-13-35)21-29(39)34-26-11-10-23(33-31(26)25-6-3-4-9-28(25)42-33)22-7-5-8-24-27(38)20-30(41-32(22)24)37-16-18-40-19-17-37/h3-11,20H,2,12-19,21H2,1H3,(H,34,39)\",[C][C][N][C][C][N][Branch2][Branch1][=Branch2][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring1][N][C][=C][C][=C][C][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][O][C][Ring1][O][=Ring1][#Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][=C][=Ring1][=Branch2][C][C][Ring2][Ring2][Branch2],2-(4-ethylpiperazin-1-yl)-n-[4-(2-morpholin-4-yl-4-oxochromen-8-yl)dibenzothiophen-1-yl]acetamide,3.05\nCOC(=O)C1C(CC2CCC1N2C)OC(=O)c3ccccc3,\"InChI=1S/C17H21NO4/c1-18-12-8-9-13(18)15(17(20)21-2)14(10-12)22-16(19)11-6-4-3-5-7-11/h3-7,12-15H,8-10H2,1-2H3\",[C][O][C][=Branch1][C][=O][C][C][Branch1][N][C][C][C][C][C][Ring1][#Branch1][N][Ring1][Branch1][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],methyl 3-(benzoyloxy)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate,1.06\nCc1ncc([N+](=O)[O-])n1CCO,\"InChI=1S/C6H9N3O3/c1-5-7-4-6(9(11)12)8(5)2-3-10/h4,10H,2-3H2,1H3\",[C][C][=N][C][=C][Branch1][=Branch1][N+1][=Branch1][C][=O][O-1][N][Ring1][Branch2][C][C][O],2-(2-methyl-5-nitroimidazol-1-yl)ethanol,-0.11\nOC1(CN2CCC1CC2)c3ccc(cc3)c4ccccc4,\"InChI=1S/C19H21NO/c21-19(14-20-12-10-18(19)11-13-20)17-8-6-16(7-9-17)15-4-2-1-3-5-15/h1-9,18,21H,10-14H2\",[O][C][Branch1][N][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],8-(4-phenylphenyl)-1-azabicyclo[2.2.2]octan-8-ol,1.5\nCSc1ncccc1C(=O)NCc2ccc(C)cc2,\"InChI=1S/C15H16N2OS/c1-11-5-7-12(8-6-11)10-17-14(18)13-4-3-9-16-15(13)19-2/h3-9H,10H2,1-2H3,(H,17,18)\",[C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],n-[(4-methylphenyl)methyl]-2-methylsulfanylpyridine-3-carboxamide,2.71\nC1Cc2ccccc2CN1c3ccncc3,\"InChI=1S/C14H14N2/c1-2-4-13-11-16(10-7-12(13)3-1)14-5-8-15-9-6-14/h1-6,8-9H,7,10-11H2\",[C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][Ring1][#Branch2][C][=C][C][=N][C][=C][Ring1][=Branch1],\"2-pyridin-4-yl-3,4-dihydro-1h-isoquinoline\",1.4\nCC(N)(COP(=O)(O)O)C(=O)O,\"InChI=1S/C4H10NO6P/c1-4(5,3(6)7)2-11-12(8,9)10/h2,5H2,1H3,(H,6,7)(H2,8,9,10)\",[C][C][Branch1][C][N][Branch1][O][C][O][P][=Branch1][C][=O][Branch1][C][O][O][C][=Branch1][C][=O][O],2-amino-2-methyl-3-phosphonooxypropanoic acid,2.5\nCC(C)CN1C(=O)N(C)C(=O)c2cn(Cc3cccc4ccccc34)cc12,\"InChI=1S/C22H23N3O2/c1-15(2)11-25-20-14-24(13-19(20)21(26)23(3)22(25)27)12-17-9-6-8-16-7-4-5-10-18(16)17/h4-10,13-15H,11-12H2,1-3H3\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1][Ring1][S],\"3-methyl-1-(2-methylpropyl)-6-(naphthalen-1-ylmethyl)pyrrolo[3,4-e]pyrimidine-2,4-dione\",4.41\nOc1ccc(cc1)C2=Cc3ccccc3OC2=O,\"InChI=1S/C15H10O3/c16-12-7-5-10(6-8-12)13-9-11-3-1-2-4-14(11)18-15(13)17/h1-9,16H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][#Branch2][=O],3-(4-hydroxyphenyl)chromen-2-one,3\nCOc1cc(OC)c2nc(C)c3CCN(c4ccc(O)cc4)c3c2c1,\"InChI=1S/C20H20N2O3/c1-12-16-8-9-22(13-4-6-14(23)7-5-13)20(16)17-10-15(24-2)11-18(25-3)19(17)21-12/h4-7,10-11,23H,8-9H2,1-3H3\",[C][O][C][=C][C][Branch1][Ring1][O][C][=C][N][=C][Branch1][C][C][C][C][C][N][Branch1][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=Ring1][N][C][Ring1][P][=C][Ring2][Ring1][#Branch1],\"4-(6,8-dimethoxy-4-methyl-2,3-dihydropyrrolo[3,2-c]quinolin-1-yl)phenol\",1.5\nCN1CCN(CC1)c2ccc3N=CN(C(=O)c3c2)c4cc(ccc4C)C(=O)Nc5ccon5,\"InChI=1S/C24H24N6O3/c1-16-3-4-17(23(31)26-22-7-12-33-27-22)13-21(16)30-15-25-20-6-5-18(14-19(20)24(30)32)29-10-8-28(2)9-11-29/h3-7,12-15H,8-11H2,1-2H3,(H,26,27,31)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][N][Branch1][O][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][N][C][C][=C][O][N][=Ring1][Branch1],\"4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3-yl]-n-(1,2-oxazol-3-yl)benzamide\",1.87\nO[C@@H](CNCCSCCCNCCc1cccc(Cl)c1)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H28ClN3O3S2/c23-16-4-1-3-15(13-16)7-9-24-8-2-11-30-12-10-25-14-19(28)17-5-6-18(27)20-21(17)31-22(29)26-20/h1,3-6,13,19,24-25,27-28H,2,7-12,14H2,(H,26,29)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][#Branch1][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"7-[(1r)-2-[2-[3-[2-(3-chlorophenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",0.98\nOC1(C(=O)Nc2ccccc12)c3ccccc3,\"InChI=1S/C14H11NO2/c16-13-14(17,10-6-2-1-3-7-10)11-8-4-5-9-12(11)15-13/h1-9,17H,(H,15,16)\",[O][C][Branch1][S][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-hydroxy-3-phenyl-1h-indol-2-one,1.71\nNC(=O)c1ccccc1O,\"InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\",[N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O],2-hydroxybenzamide,1.09\nOCC(CO)NC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C21H21ClN4O5S/c22-17-7-12-6-14(25-20(12)32-17)19(30)24-15-5-11-3-1-2-4-16(11)26(21(15)31)8-18(29)23-13(9-27)10-28/h1-4,6-7,13,15,25,27-28H,5,8-10H2,(H,23,29)(H,24,30)\",[O][C][C][Branch1][Ring1][C][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-[2-(1,3-dihydroxypropan-2-ylamino)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",2.61\nCC(C)Oc1cc(OCCN2CCOCC2)cc3ncnc(Nc4c(Cl)ccc5OCOc45)c13,\"InChI=1S/C24H27ClN4O5/c1-15(2)34-20-12-16(31-10-7-29-5-8-30-9-6-29)11-18-21(20)24(27-13-26-18)28-22-17(25)3-4-19-23(22)33-14-32-19/h3-4,11-13,15H,5-10,14H2,1-2H3,(H,26,27,28)\",[C][C][Branch1][C][C][O][C][=C][C][Branch1][N][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=C][Ring2][Ring1][=C][Ring1][P],\"n-(5-chloro-1,3-benzodioxol-4-yl)-7-(2-morpholin-4-ylethoxy)-5-propan-2-yloxyquinazolin-4-amine\",3.68\nNC(Cc1ccccc1)c2ccccc2,\"InChI=1S/C14H15N/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10,14H,11,15H2\",[N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1,2-di(phenyl)ethanamine\",1.32\nCCOC(=O)c1ccc(OC(=O)CCCCCN=C(N)N)cc1,\"InChI=1S/C16H23N3O4/c1-2-22-15(21)12-7-9-13(10-8-12)23-14(20)6-4-3-5-11-19-16(17)18/h7-10H,2-6,11H2,1H3,(H4,17,18,19)\",[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][P][O][C][=Branch1][C][=O][C][C][C][C][C][N][=C][Branch1][C][N][N][C][=C][Ring2][Ring1][C],ethyl 4-[6-(diaminomethylideneamino)hexanoyloxy]benzoate,2.41\nCOc1ccc2c(c1)[nH]c3c(C)nccc23,\"InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3\",[C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][NH1][C][=C][Branch1][C][C][N][=C][C][=C][Ring1][O][Ring1][#Branch1],\"7-methoxy-1-methyl-9h-pyrido[3,4-b]indole\",2.9\nOCCNCCNc1ccc2c(NC(=O)CC34CC5CC(CC(C5)C3)C4)cccc2n1,\"InChI=1S/C25H34N4O2/c30-9-8-26-6-7-27-23-5-4-20-21(28-23)2-1-3-22(20)29-24(31)16-25-13-17-10-18(14-25)12-19(11-17)15-25/h1-5,17-19,26,30H,6-16H2,(H,27,28)(H,29,31)\",[O][C][C][N][C][C][N][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][C][=C][C][Ring2][Ring1][Ring2][=N][Ring2][Ring1][Branch2],2-(1-adamantyl)-n-[2-[2-(2-hydroxyethylamino)ethylamino]quinolin-5-yl]acetamide,1.79\nCc1ccc(COC(=O)N2CC[C@H](CNc3ncccn3)[C@H](F)C2)cc1,\"InChI=1S/C19H23FN4O2/c1-14-3-5-15(6-4-14)13-26-19(25)24-10-7-16(17(20)12-24)11-23-18-21-8-2-9-22-18/h2-6,8-9,16-17H,7,10-13H2,1H3,(H,21,22,23)/t16-,17-/m1/s1\",[C][C][=C][C][=C][Branch2][Ring1][=C][C][O][C][=Branch1][C][=O][N][C][C][C@H1][Branch1][O][C][N][C][=N][C][=C][C][=N][Ring1][=Branch1][C@H1][Branch1][C][F][C][Ring1][#C][C][=C][Ring2][Ring1][=Branch2],\"(4-methylphenyl)methyl (3s,4r)-3-fluoro-4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate\",3.21\nClc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4ccncc4)C3=O,\"InChI=1S/C17H11ClN4O3/c18-10-1-2-11-12(7-10)20-14-13(15(11)23)17(25)22(21-16(14)24)8-9-3-5-19-6-4-9/h1-7H,8H2,(H,20,23)(H,21,24)\",[Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][#Branch2][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Ring1][P][=O],\"7-chloro-2-(pyridin-4-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",-0.16\nC[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO,\"InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,17+,19+,20+,21+,22+/m1/s1\",[C][C@@H1][C][C@H1][C@@H1][C][C][C][=C][C][=Branch1][C][=O][C][=C][C@][Ring1][#Branch1][Branch1][C][C][C@@][Ring1][N][Branch1][C][F][C@@H1][Branch1][C][O][C][C@][Ring2][Ring1][C][Branch1][C][C][C@@][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O],\"(8s,9r,10s,11s,13s,14s,16r,17r)-9-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one\",1.87\nCOc1cccc(c1)S(=O)(=O)c2c(C)n(CC(=O)O)c3ccc(C)cc23,\"InChI=1S/C19H19NO5S/c1-12-7-8-17-16(9-12)19(13(2)20(17)11-18(21)22)26(23,24)15-6-4-5-14(10-15)25-3/h4-10H,11H2,1-3H3,(H,21,22)\",[C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch1][C][C][N][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#C][Ring1][#Branch1],\"2-[3-(3-methoxyphenyl)sulfonyl-2,5-dimethylindol-1-yl]acetic acid\",-0.42\nO=C(C1CCN(CC1)c2nnc(s2)n3cccc3)N4CCN(Cc5ccc6OCOc6c5)CC4,\"InChI=1S/C24H28N6O3S/c31-22(19-5-9-30(10-6-19)24-26-25-23(34-24)29-7-1-2-8-29)28-13-11-27(12-14-28)16-18-3-4-20-21(15-18)33-17-32-20/h1-4,7-8,15,19H,5-6,9-14,16-17H2\",[O][=C][Branch2][Ring1][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][N][C][=C][C][=C][Ring1][Branch1][N][C][C][N][Branch1][#C][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][C][Ring1][S],\"[4-(1,3-benzodioxol-5-ylmethyl)piperazin-1-yl]-[1-(5-pyrrol-1-yl-1,3,4-thiadiazol-2-yl)piperidin-4-yl]methanone\",2.5\nCOc1cc2c(Nc3ccc(Br)cc3F)ncnc2cc1OC[C@@H]4CCCN(C)C4,\"InChI=1S/C22H24BrFN4O2/c1-28-7-3-4-14(11-28)12-30-21-10-19-16(9-20(21)29-2)22(26-13-25-19)27-18-6-5-15(23)8-17(18)24/h5-6,8-10,13-14H,3-4,7,11-12H2,1-2H3,(H,25,26,27)/t14-/m1/s1\",[C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C@@H1][C][C][C][N][Branch1][C][C][C][Ring1][#Branch1],n-(4-bromo-2-fluorophenyl)-6-methoxy-7-[[(3r)-1-methylpiperidin-3-yl]methoxy]quinazolin-4-amine,3.05\nOc1ccccc1OCC(=O)NC2CCCC2,\"InChI=1S/C13H17NO3/c15-11-7-3-4-8-12(11)17-9-13(16)14-10-5-1-2-6-10/h3-4,7-8,10,15H,1-2,5-6,9H2,(H,14,16)\",[O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1],n-cyclopentyl-2-(2-hydroxyphenoxy)acetamide,2.31\nClc1ccc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)C5CCNCC5,\"InChI=1S/C23H31ClN2O/c24-21-2-1-19(18-3-5-25-6-4-18)10-20(21)22(27)26-14-23-11-15-7-16(12-23)9-17(8-15)13-23/h1-2,10,15-18,25H,3-9,11-14H2,(H,26,27)\",[Cl][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][C][C][C][N][C][C][Ring1][=Branch1],n-(1-adamantylmethyl)-2-chloro-5-piperidin-4-ylbenzamide,1.58\nClc1ccc(N2CCN(CC2)C(=O)COCc3ccncc3)c(Cl)c1,\"InChI=1S/C18H19Cl2N3O2/c19-15-1-2-17(16(20)11-15)22-7-9-23(10-8-22)18(24)13-25-12-14-3-5-21-6-4-14/h1-6,11H,7-10,12-13H2\",[Cl][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2],\"1-[4-(2,4-dichlorophenyl)piperazin-1-yl]-2-(pyridin-4-ylmethoxy)ethanone\",3.38\nCCOC(=O)N1CCN(CC1)C(=O)[C@H](Cc2cccc(c2)C(=N)N)NS(=O)(=O)c3c(cc(cc3C(C)C)C(C)C)C(C)C,\"InChI=1S/C32H47N5O5S/c1-8-42-32(39)37-14-12-36(13-15-37)31(38)28(17-23-10-9-11-24(16-23)30(33)34)35-43(40,41)29-26(21(4)5)18-25(20(2)3)19-27(29)22(6)7/h9-11,16,18-22,28,35H,8,12-15,17H2,1-7H3,(H3,33,34)/t28-/m0/s1\",[C][C][O][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][Branch1][P][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=N][N][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][C][Branch1][C][C][C][C][Branch1][C][C][C][C][Branch1][C][C][C],\"ethyl 4-[(2s)-3-(3-carbamimidoylphenyl)-2-[[2,4,6-tri(propan-2-yl)phenyl]sulfonylamino]propanoyl]piperazine-1-carboxylate\",1.67\nCC1(C)CC(=O)c2c(N)c3ccccc3nc2C1,\"InChI=1S/C15H16N2O/c1-15(2)7-11-13(12(18)8-15)14(16)9-5-3-4-6-10(9)17-11/h3-6H,7-8H2,1-2H3,(H2,16,17)\",[C][C][Branch1][C][C][C][C][=Branch1][C][=O][C][=C][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][O][C][Ring1][P],\"9-amino-3,3-dimethyl-2,4-dihydroacridin-1-one\",3\nC[S+]([O-])CCN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C19H18ClN3O3S2/c1-28(26)7-6-23-15-5-3-2-4-11(15)8-14(19(23)25)21-17(24)13-9-12-10-16(20)27-18(12)22-13/h2-5,9-10,14,22H,6-8H2,1H3,(H,21,24)\",[C][S+1][Branch1][C][O-1][C][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-(2-methylsulfinylethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.17\nClc1c(ccnc1N2CCNCC2)C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C21H29ClN4O/c22-18-17(1-2-24-19(18)26-5-3-23-4-6-26)20(27)25-13-21-10-14-7-15(11-21)9-16(8-14)12-21/h1-2,14-16,23H,3-13H2,(H,25,27)\",[Cl][C][=C][Branch1][#C][C][=C][N][=C][Ring1][=Branch1][N][C][C][N][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-3-chloro-2-piperazin-1-ylpyridine-4-carboxamide,1.77\nO[C@H](CNC(=O)C1=CNC(=O)c2ccccc12)CN3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C24H25Cl2N3O4/c25-21-6-5-17(11-22(21)26)33-16-7-9-29(10-8-16)14-15(30)12-27-24(32)20-13-28-23(31)19-4-2-1-3-18(19)20/h1-6,11,13,15-16,30H,7-10,12,14H2,(H,27,32)(H,28,31)/t15-/m1/s1\",[O][C@H1][Branch2][Ring1][Branch2][C][N][C][=Branch1][C][=O][C][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"n-[(2r)-3-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-2-hydroxypropyl]-1-oxo-2h-isoquinoline-4-carboxamide\",3.42\nCCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3ccccc3,\"InChI=1S/C23H28N2O/c1-3-25(4-2)23(26)21-12-10-19(11-13-21)22(18-8-6-5-7-9-18)20-14-16-24-17-15-20/h5-13,24H,3-4,14-17H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n,n-diethyl-4-(phenyl-piperidin-4-ylidenemethyl)benzamide\",1.2\nFc1ccc(cc1)C(=O)N2CCC[C@@H](C2)c3onc(n3)c4ccc(F)cc4,\"InChI=1S/C20H17F2N3O2/c21-16-7-3-13(4-8-16)18-23-19(27-24-18)15-2-1-11-25(12-15)20(26)14-5-9-17(22)10-6-14/h3-10,15H,1-2,11-12H2/t15-/m0/s1\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C@@H1][Branch1][Ring2][C][Ring1][=Branch1][C][O][N][=C][Branch1][Ring2][N][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"(4-fluorophenyl)-[(3s)-3-[3-(4-fluorophenyl)-1,2,4-oxadiazol-5-yl]piperidin-1-yl]methanone\",3.73\nCC(C)c1c(O)c(O)c(C=O)c2c(O)c(c(C)cc12)c3c(C)cc4c(C(C)C)c(O)c(O)c(C=O)c4c3O,\"InChI=1S/C30H30O8/c1-11(2)19-15-7-13(5)21(27(35)23(15)17(9-31)25(33)29(19)37)22-14(6)8-16-20(12(3)4)30(38)26(34)18(10-32)24(16)28(22)36/h7-12,33-38H,1-6H3\",[C][C][Branch1][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Branch1][Ring1][C][=O][C][=C][Branch1][C][O][C][=Branch1][O][=C][Branch1][C][C][C][=C][Ring1][S][Ring1][Branch2][C][=C][Branch1][C][C][C][=C][C][Branch1][=Branch1][C][Branch1][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Branch1][Ring1][C][=O][C][Ring1][=N][=C][Ring2][Ring1][C][O],\"7-(8-formyl-1,6,7-trihydroxy-3-methyl-5-propan-2-ylnaphthalen-2-yl)-2,3,8-trihydroxy-6-methyl-4-propan-2-ylnaphthalene-1-carbaldehyde\",2.75\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3ccc[n+]([O-])c3)C(=O)C(F)(F)F,\"InChI=1S/C26H26F3N5O5/c1-16(2)22(23(36)26(27,28)29)32-21(35)15-34-20(18-8-4-3-5-9-18)11-10-19(24(34)37)31-25(38)30-13-17-7-6-12-33(39)14-17/h3-12,14,16,22H,13,15H2,1-2H3,(H,32,35)(H2,30,31,38)\",[C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][N+1][Branch1][C][O-1][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[3-[(1-oxidopyridin-1-ium-3-yl)methylcarbamoylamino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.48\nCCS(=O)(=O)c1ccc(Oc2cc3nc([nH]c3cc2CN4C(=O)CCC4=O)c5ccccn5)cc1,\"InChI=1S/C25H22N4O5S/c1-2-35(32,33)18-8-6-17(7-9-18)34-22-14-21-20(27-25(28-21)19-5-3-4-12-26-19)13-16(22)15-29-23(30)10-11-24(29)31/h3-9,12-14H,2,10-11,15H2,1H3,(H,27,28)\",[C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][=Branch1][O][C][=C][C][N][=C][Branch2][Ring1][Branch1][NH1][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring2][Ring1][=C],\"1-[[6-(4-ethylsulfonylphenoxy)-2-pyridin-2-yl-3h-benzimidazol-5-yl]methyl]pyrrolidine-2,5-dione\",2\nClc1ccc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)N5N=CC(=O)NC5=O,\"InChI=1S/C21H23ClN4O3/c22-17-2-1-15(26-20(29)25-18(27)10-24-26)6-16(17)19(28)23-11-21-7-12-3-13(8-21)5-14(4-12)9-21/h1-2,6,10,12-14H,3-5,7-9,11H2,(H,23,28)(H,25,27,29)\",[Cl][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O],\"n-(1-adamantylmethyl)-2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)benzamide\",2.1\nCCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)O,\"InChI=1S/C16H20N4O/c1-4-12-19-13-14(20(12)9-16(2,3)21)10-7-5-6-8-11(10)18-15(13)17/h5-8,21H,4,9H2,1-3H3,(H2,17,18)\",[C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][Branch1][C][C][O],\"1-(4-amino-2-ethylimidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol\",1.38\nO=C(Nc1nccs1)c2ccccc2,\"InChI=1S/C10H8N2OS/c13-9(8-4-2-1-3-5-8)12-10-11-6-7-14-10/h1-7H,(H,11,12,13)\",[O][=C][Branch1][=Branch2][N][C][=N][C][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-(1,3-thiazol-2-yl)benzamide\",2.43\nFc1ccc(cc1Cl)C(=O)Nc2ccc(Cl)nc2,\"InChI=1S/C12H7Cl2FN2O/c13-9-5-7(1-3-10(9)15)12(18)17-8-2-4-11(14)16-6-8/h1-6H,(H,17,18)\",[F][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][N][=C][Ring1][#Branch1],3-chloro-n-(6-chloropyridin-3-yl)-4-fluorobenzamide,3.64\nCC(C)NC(=O)NS(=O)(=O)c1cnccc1Nc2cccc(C)c2,\"InChI=1S/C16H20N4O3S/c1-11(2)18-16(21)20-24(22,23)15-10-17-8-7-14(15)19-13-6-4-5-12(3)9-13/h4-11H,1-3H3,(H,17,19)(H2,18,20,21)\",[C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][N][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1],3-[4-[(3-methylphenyl)amino]pyridin-3-yl]sulfonyl-1-propan-2-ylurea,0.3\nNC(=O)c1sc(cc1N)c2ccc(Cl)cc2,\"InChI=1S/C11H9ClN2OS/c12-7-3-1-6(2-4-7)9-5-8(13)10(16-9)11(14)15/h1-5H,13H2,(H2,14,15)\",[N][C][=Branch1][C][=O][C][S][C][=Branch1][=Branch1][=C][C][=Ring1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],3-amino-5-(4-chlorophenyl)thiophene-2-carboxamide,3.3\nCN1C(=O)N(Cc2ccc(Br)cc2)c3ccccc13,\"InChI=1S/C15H13BrN2O/c1-17-13-4-2-3-5-14(13)18(15(17)19)10-11-6-8-12(16)9-7-11/h2-9H,10H2,1H3\",[C][N][C][=Branch1][C][=O][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1],1-[(4-bromophenyl)methyl]-3-methylbenzimidazol-2-one,2.81\nCOc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC4CCN(CC4)S(=O)(=O)C,\"InChI=1S/C21H22ClFN4O4S/c1-30-18-11-17-14(10-19(18)31-13-6-8-27(9-7-13)32(2,28)29)21(25-12-24-17)26-16-5-3-4-15(22)20(16)23/h3-5,10-13H,6-9H2,1-2H3,(H,24,25,26)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-(3-chloro-2-fluorophenyl)-7-methoxy-6-(1-methylsulfonylpiperidin-4-yl)oxyquinazolin-4-amine,2.82\nCC1(C)C(=O)Nc2ccccc12,\"InChI=1S/C10H11NO/c1-10(2)7-5-3-4-6-8(7)11-9(10)12/h3-6H,1-2H3,(H,11,12)\",[C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1],\"3,3-dimethyl-1h-indol-2-one\",2.3\nCNS(=O)(=O)CCc1ccc2[nH]cc(C3CCN(C)CC3)c2c1,\"InChI=1S/C17H25N3O2S/c1-18-23(21,22)10-7-13-3-4-17-15(11-13)16(12-19-17)14-5-8-20(2)9-6-14/h3-4,11-12,14,18-19H,5-10H2,1-2H3\",[C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][=C][C][=C][NH1][C][=C][Branch1][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][Ring1][N][=C][Ring1][S],n-methyl-2-[3-(1-methylpiperidin-4-yl)-1h-indol-5-yl]ethanesulfonamide,0.48\nO=C1Nc2ccc(cc2C1=O)S(=O)(=O)N3CCC[C@H]3CNc4ccccc4,\"InChI=1S/C19H19N3O4S/c23-18-16-11-15(8-9-17(16)21-19(18)24)27(25,26)22-10-4-7-14(22)12-20-13-5-2-1-3-6-13/h1-3,5-6,8-9,11,14,20H,4,7,10,12H2,(H,21,23,24)/t14-/m0/s1\",[O][=C][N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-[(2s)-2-[(phenylamino)methyl]pyrrolidin-1-yl]sulfonyl-1h-indole-2,3-dione\",2.4\nFc1ccc(cc1)C(=O)N2CCC(CC2)C(=O)c3ccc(Cl)cc3,\"InChI=1S/C19H17ClFNO2/c20-16-5-1-13(2-6-16)18(23)14-9-11-22(12-10-14)19(24)15-3-7-17(21)8-4-15/h1-8,14H,9-12H2\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],(4-chlorophenyl)-[1-(4-fluorobenzoyl)piperidin-4-yl]methanone,3.49\nCC(C)(N)C(=O)N[C@H](COCc1ccccc1)C(=O)N2CCC3(CC2)CN(c4ccccc34)S(=O)(=O)C,\"InChI=1S/C27H36N4O5S/c1-26(2,28)25(33)29-22(18-36-17-20-9-5-4-6-10-20)24(32)30-15-13-27(14-16-30)19-31(37(3,34)35)23-12-8-7-11-21(23)27/h4-12,22H,13-19,28H2,1-3H3,(H,29,33)/t22-/m1/s1\",[C][C][Branch1][C][C][Branch1][C][N][C][=Branch1][C][=O][N][C@H1][Branch1][N][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][N][Branch1][O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],\"2-amino-2-methyl-n-[(2r)-1-(1-methylsulfonylspiro[2h-indole-3,4'-piperidine]-1'-yl)-1-oxo-3-(phenylmethoxy)propan-2-yl]propanamide\",1.4\nCC(C)(C)NC(=O)Nc1ccc(cc1)c2c(N)nc(N)nc2COCc3ccccc3,\"InChI=1S/C23H28N6O2/c1-23(2,3)29-22(30)26-17-11-9-16(10-12-17)19-18(27-21(25)28-20(19)24)14-31-13-15-7-5-4-6-8-15/h4-12H,13-14H2,1-3H3,(H2,26,29,30)(H4,24,25,27,28)\",[C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][Branch1][C][N][N][=C][Branch1][C][N][N][=C][Ring1][Branch2][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-tert-butyl-3-[4-[2,4-diamino-6-(phenylmethoxymethyl)pyrimidin-5-yl]phenyl]urea\",3.09\nCCCNC[C@H](O)COc1ccccc1C(=O)CCc2ccccc2,\"InChI=1S/C21H27NO3/c1-2-14-22-15-18(23)16-25-21-11-7-6-10-19(21)20(24)13-12-17-8-4-3-5-9-17/h3-11,18,22-23H,2,12-16H2,1H3/t18-/m0/s1\",[C][C][C][N][C][C@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],1-[2-[(2s)-2-hydroxy-3-propylaminopropoxy]phenyl]-3-phenylpropan-1-one,1.69\nCC(=O)Nc1nc(cs1)c2cccs2,\"InChI=1S/C9H8N2OS2/c1-6(12)10-9-11-7(5-14-9)8-3-2-4-13-8/h2-5H,1H3,(H,10,11,12)\",[C][C][=Branch1][C][=O][N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1],\"n-(4-thiophen-2-yl-1,3-thiazol-2-yl)acetamide\",2.77\nO=C1N(Cc2ccccc12)C3CCN(CCC(c4ccccc4)c5ccccc5)CC3,\"InChI=1S/C28H30N2O/c31-28-27-14-8-7-13-24(27)21-30(28)25-15-18-29(19-16-25)20-17-26(22-9-3-1-4-10-22)23-11-5-2-6-12-23/h1-14,25-26H,15-21H2\",[O][=C][N][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][C][C][N][Branch2][Ring1][=Branch1][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch1],\"2-[1-[3,3-di(phenyl)propyl]piperidin-4-yl]-3h-isoindol-1-one\",4.1\n[O-][N+](=O)c1cccc(c1)c2ccc(OCC(CCc3ccc(cc3)C(=O)N4CCCC4)N5C(=O)CCCC5=O)cc2,\"InChI=1S/C32H33N3O6/c36-30-7-4-8-31(37)34(30)28(16-11-23-9-12-25(13-10-23)32(38)33-19-1-2-20-33)22-41-29-17-14-24(15-18-29)26-5-3-6-27(21-26)35(39)40/h3,5-6,9-10,12-15,17-18,21,28H,1-2,4,7-8,11,16,19-20,22H2\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring2][#Branch2][O][C][C][Branch2][Ring1][Branch2][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][N][C][=Branch1][C][=O][C][C][C][C][Ring1][#Branch1][=O][C][=C][Ring2][Ring1][S],\"1-[1-[4-(3-nitrophenyl)phenoxy]-4-[4-(pyrrolidine-1-carbonyl)phenyl]butan-2-yl]piperidine-2,6-dione\",2.31\nCC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)N4CCN(CC4)C(=O)CO)ncc2F,\"InChI=1S/C23H28FN7O2/c1-15(2)31-16(3)25-13-20(31)22-19(24)12-26-23(28-22)27-17-4-6-18(7-5-17)29-8-10-30(11-9-29)21(33)14-32/h4-7,12-13,15,32H,8-11,14H2,1-3H3,(H,26,27,28)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][=N][C][=C][Ring2][Ring1][#Branch1][F],1-[4-[4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]piperazin-1-yl]-2-hydroxyethanone,2.19\nCC(C)[C@H](NC(=O)CCc1ccccc1)C(=O)N2CCCC2,\"InChI=1S/C18H26N2O2/c1-14(2)17(18(22)20-12-6-7-13-20)19-16(21)11-10-15-8-4-3-5-9-15/h3-5,8-9,14,17H,6-7,10-13H2,1-2H3,(H,19,21)/t17-/m0/s1\",[C][C][Branch1][C][C][C@H1][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1],n-[(2s)-3-methyl-1-oxo-1-pyrrolidin-1-ylbutan-2-yl]-3-phenylpropanamide,2.49\nCOc1ccccc1C(=O)Nc2nc3ccccc3s2,\"InChI=1S/C15H12N2O2S/c1-19-12-8-4-2-6-10(12)14(18)17-15-16-11-7-3-5-9-13(11)20-15/h2-9H,1H3,(H,16,17,18)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2],\"n-(1,3-benzothiazol-2-yl)-2-methoxybenzamide\",3.61\nCOc1ccc(cc1)c2csc(n2)N(CCCN3CCOCC3)C(=O)c4occc4,\"InChI=1S/C22H25N3O4S/c1-27-18-7-5-17(6-8-18)19-16-30-22(23-19)25(21(26)20-4-2-13-29-20)10-3-9-24-11-14-28-15-12-24/h2,4-8,13,16H,3,9-12,14-15H2,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][S][C][=Branch1][Ring2][=N][Ring1][Branch1][N][Branch1][N][C][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1],\"n-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-n-(3-morpholin-4-ylpropyl)furan-2-carboxamide\",3.34\nCCCSc1nc(N[C@@H]2C[C@H]2c3ccccc3)c4nnn([C@@H]5C[C@H](CO)[C@@H](O)[C@H]5O)c4n1,\"InChI=1S/C22H28N6O3S/c1-2-8-32-22-24-20(23-15-10-14(15)12-6-4-3-5-7-12)17-21(25-22)28(27-26-17)16-9-13(11-29)18(30)19(16)31/h3-7,13-16,18-19,29-31H,2,8-11H2,1H3,(H,23,24,25)/t13-,14+,15-,16-,18-,19+/m1/s1\",[C][C][C][S][C][=N][C][Branch1][#C][N][C@@H1][C][C@H1][Ring1][Ring1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][N][=N][N][Branch1][S][C@@H1][C][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O][C][Ring1][=C][=N][Ring2][Ring1][N],\"(1s,2r,3r,5r)-3-(hydroxymethyl)-5-[7-[[(1r,2s)-2-phenylcyclopropyl]amino]-5-propylsulfanyltriazolo[5,4-d]pyrimidin-3-yl]cyclopentane-1,2-diol\",3.99\nOC(CN1CCCCC1)(C(=O)c2ccccc2)c3ccccc3,\"InChI=1S/C20H23NO2/c22-19(17-10-4-1-5-11-17)20(23,18-12-6-2-7-13-18)16-21-14-8-3-9-15-21/h1-2,4-7,10-13,23H,3,8-9,14-16H2\",[O][C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-hydroxy-1,2-di(phenyl)-3-piperidin-1-ylpropan-1-one\",3.41\nCCc1ccc(CCNCCCSCCNC[C@H](O)c2ccc(O)c3NC(=O)Sc23)cc1,\"InChI=1S/C24H33N3O3S2/c1-2-17-4-6-18(7-5-17)10-12-25-11-3-14-31-15-13-26-16-21(29)19-8-9-20(28)22-23(19)32-24(30)27-22/h4-9,21,25-26,28-29H,2-3,10-16H2,1H3,(H,27,30)/t21-/m0/s1\",[C][C][C][=C][C][=C][Branch2][Ring2][Ring1][C][C][N][C][C][C][S][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1][C][=C][Ring2][Ring1][=C],\"7-[(1r)-2-[2-[3-[2-(4-ethylphenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",0.86\nCN1CCN(CC1)S(=O)(=O)c2ccc(c(C)c2)c3cnc(N)c(n3)C(=O)Nc4cccnc4,\"InChI=1S/C22H25N7O3S/c1-15-12-17(33(31,32)29-10-8-28(2)9-11-29)5-6-18(15)19-14-25-21(23)20(27-19)22(30)26-16-4-3-7-24-13-16/h3-7,12-14H,8-11H2,1-2H3,(H2,23,25)(H,26,30)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1],3-amino-6-[2-methyl-4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-pyridin-3-ylpyrazine-2-carboxamide,2.6\nCN(C)c1nc(nc(n1)N(C)C)N(C)C,InChI=1S/C9H18N6/c1-13(2)7-10-8(14(3)4)12-9(11-7)15(5)6/h1-6H3,[C][N][Branch1][C][C][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C],\"n2,n2,n4,n4,n6,n6-hexamethyl-1,3,5-triazine-2,4,6-triamine\",2.44\nCOC(=O)c1ccc(NC(=O)c2cc(OC)c(OC)c(OC)c2)cc1,\"InChI=1S/C18H19NO6/c1-22-14-9-12(10-15(23-2)16(14)24-3)17(20)19-13-7-5-11(6-8-13)18(21)25-4/h5-10H,1-4H3,(H,19,20)\",[C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][=Branch1][C][=O][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][N][C][=C][Ring2][Ring1][Branch1],\"methyl 4-[(3,4,5-trimethoxybenzoyl)amino]benzoate\",3.2\nO=C(CS(=O)(=O)c1ccccc1)c2ccccc2,\"InChI=1S/C14H12O3S/c15-14(12-7-3-1-4-8-12)11-18(16,17)13-9-5-2-6-10-13/h1-10H,11H2\",[O][=C][Branch1][P][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],1-phenyl-2-phenylsulfonylethanone,1.86\nCc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)cc4C,\"InChI=1S/C25H32ClN3O4S/c1-18-3-6-23(7-4-18)34(31,32)27-25(30)29-13-9-21(10-14-29)28-15-11-22(12-16-28)33-24-8-5-20(26)17-19(24)2/h3-8,17,21-22H,9-16H2,1-2H3,(H,27,30)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C],4-[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide,1.79\nCOc1cccc(NC(=O)CC23CC4CC(CC(C4)C2)C3)c1C,\"InChI=1S/C20H27NO2/c1-13-17(4-3-5-18(13)23-2)21-19(22)12-20-9-14-6-15(10-20)8-16(7-14)11-20/h3-5,14-16H,6-12H2,1-2H3,(H,21,22)\",[C][O][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][C],2-(1-adamantyl)-n-(3-methoxy-2-methylphenyl)acetamide,4.21\nO=C(Cc1ccccc1)Nc2nccs2,\"InChI=1S/C11H10N2OS/c14-10(13-11-12-6-7-15-11)8-9-4-2-1-3-5-9/h1-7H,8H2,(H,12,13,14)\",[O][=C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=N][C][=C][S][Ring1][Branch1],\"2-phenyl-n-(1,3-thiazol-2-yl)acetamide\",2.5\nO=C(Cc1cccc2ccccc12)Nc3ccccc3,\"InChI=1S/C18H15NO/c20-18(19-16-10-2-1-3-11-16)13-15-9-6-8-14-7-4-5-12-17(14)15/h1-12H,13H2,(H,19,20)\",[O][=C][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],2-naphthalen-1-yl-n-phenylacetamide,3.9\nCNC1(C)C2CCC(C2)C1(C)C,\"InChI=1S/C11H21N/c1-10(2)8-5-6-9(7-8)11(10,3)12-4/h8-9,12H,5-7H2,1-4H3\",[C][N][C][Branch1][C][C][C][C][C][C][Branch1][Ring2][C][Ring1][Branch1][C][Ring1][Branch2][Branch1][C][C][C],\"n,5,6,6-tetramethylbicyclo[2.2.1]heptan-5-amine\",-0.84\nCC(C)C(=O)Nc1ccc(c(c1)C(F)(F)F)[N+](=O)[O-],\"InChI=1S/C11H11F3N2O3/c1-6(2)10(17)15-7-3-4-9(16(18)19)8(5-7)11(12,13)14/h3-6H,1-2H3,(H,15,17)\",[C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][N+1][=Branch1][C][=O][O-1],2-methyl-n-[4-nitro-3-(trifluoromethyl)phenyl]propanamide,3.46\nCOc1cc(cc(OC)c1OC)C(=O)N2CC[C@@](CCN3CCC(CC3)(C(=O)N)c4ccccc4)(C2)c5ccc(Cl)c(Cl)c5,\"InChI=1S/C34H39Cl2N3O5/c1-42-28-19-23(20-29(43-2)30(28)44-3)31(40)39-18-12-33(22-39,25-9-10-26(35)27(36)21-25)11-15-38-16-13-34(14-17-38,32(37)41)24-7-5-4-6-8-24/h4-10,19-21H,11-18,22H2,1-3H3,(H2,37,41)/t33-/m0/s1\",[C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][N][C][C][C@@][Branch2][Ring1][N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][Branch1][Branch1][C][Ring2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"1-[2-[(3r)-3-(3,4-dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]-4-phenylpiperidine-4-carboxamide\",3.23\nC[C@@H](Oc1cccc2ncnc(Nc3ccc4c(cnn4Cc5cscn5)c3)c12)C(=O)N6CCOCC6,\"InChI=1S/C26H25N7O3S/c1-17(26(34)32-7-9-35-10-8-32)36-23-4-2-3-21-24(23)25(28-15-27-21)31-19-5-6-22-18(11-19)12-30-33(22)13-20-14-37-16-29-20/h2-6,11-12,14-17H,7-10,13H2,1H3,(H,27,28,31)/t17-/m1/s1\",[C][C@@H1][Branch2][Ring2][=N][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][C][Branch1][=C][C][=N][N][Ring1][Branch1][C][C][=C][S][C][=N][Ring1][Branch1][=C][Ring1][#C][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1],\"(2r)-1-morpholin-4-yl-2-[4-[[1-(1,3-thiazol-4-ylmethyl)indazol-5-yl]amino]quinazolin-5-yl]oxypropan-1-one\",2.81\nO=S(=O)(Nc1cccnc1)c2cccs2,\"InChI=1S/C9H8N2O2S2/c12-15(13,9-4-2-6-14-9)11-8-3-1-5-10-7-8/h1-7,11H\",[O][=S][=Branch1][C][=O][Branch1][#Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][S][Ring1][Branch1],n-pyridin-3-ylthiophene-2-sulfonamide,0.54\nBrc1ccc(cc1)C(=O)Cn2cnc3ccccc23,\"InChI=1S/C15H11BrN2O/c16-12-7-5-11(6-8-12)15(19)9-18-10-17-13-3-1-2-4-14(13)18/h1-8,10H,9H2\",[Br][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1],2-(benzimidazol-1-yl)-1-(4-bromophenyl)ethanone,3.22\nCCCc1nc2c(N)nc3ccccc3c2s1,\"InChI=1S/C13H13N3S/c1-2-5-10-16-11-12(17-10)8-6-3-4-7-9(8)15-13(11)14/h3-4,6-7H,2,5H2,1H3,(H2,14,15)\",[C][C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][S][Ring1][=C],\"2-propyl-[1,3]thiazolo[4,5-c]quinolin-4-amine\",4.09\nOC(=O)C1Cc2c([nH]c3ccccc23)C(N1)c4ccccc4,\"InChI=1S/C18H16N2O2/c21-18(22)15-10-13-12-8-4-5-9-14(12)19-17(13)16(20-15)11-6-2-1-3-7-11/h1-9,15-16,19-20H,10H2,(H,21,22)\",[O][C][=Branch1][C][=O][C][C][C][=C][Branch1][N][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][Branch1][Ring2][N][Ring1][=N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-phenyl-2,3,4,9-tetrahydro-1h-pyrido[5,4-b]indole-3-carboxylic acid\",0.78\nCOc1cc(CNc2nc3ccccc3[nH]2)cc(OC)c1OC,\"InChI=1S/C17H19N3O3/c1-21-14-8-11(9-15(22-2)16(14)23-3)10-18-17-19-12-6-4-5-7-13(12)20-17/h4-9H,10H2,1-3H3,(H2,18,19,20)\",[C][O][C][=C][C][Branch1][S][C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][=C][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][Ring1][O][C],\"n-[(3,4,5-trimethoxyphenyl)methyl]-1h-benzimidazol-2-amine\",2.36\nCCn1c2ccccc2c3cc(NC(=O)C(C)C)ccc13,\"InChI=1S/C18H20N2O/c1-4-20-16-8-6-5-7-14(16)15-11-13(9-10-17(15)20)19-18(21)12(2)3/h5-12H,4H2,1-3H3,(H,19,21)\",[C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][N],n-(9-ethylcarbazol-3-yl)-2-methylpropanamide,4.2\nCOc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OC[C@@H]4CCCN(C)C4,\"InChI=1S/C22H24ClFN4O2/c1-28-7-3-4-14(11-28)12-30-21-10-19-16(9-20(21)29-2)22(26-13-25-19)27-18-6-5-15(23)8-17(18)24/h5-6,8-10,13-14H,3-4,7,11-12H2,1-2H3,(H,25,26,27)/t14-/m1/s1\",[C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C@@H1][C][C][C][N][Branch1][C][C][C][Ring1][#Branch1],n-(4-chloro-2-fluorophenyl)-6-methoxy-7-[[(3r)-1-methylpiperidin-3-yl]methoxy]quinazolin-4-amine,2.9\nCc1ccc(cc1)S(=O)(=O)N2CCN(CC2)C(=O)c3occc3,\"InChI=1S/C16H18N2O4S/c1-13-4-6-14(7-5-13)23(20,21)18-10-8-17(9-11-18)16(19)15-3-2-12-22-15/h2-7,12H,8-11H2,1H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1],furan-2-yl-[4-(4-methylphenyl)sulfonylpiperazin-1-yl]methanone,2.17\nCc1ccc(CN2C(=O)CCSc3ccc(Cl)cc23)cc1,\"InChI=1S/C17H16ClNOS/c1-12-2-4-13(5-3-12)11-19-15-10-14(18)6-7-16(15)21-9-8-17(19)20/h2-7,10H,8-9,11H2,1H3\",[C][C][=C][C][=C][Branch2][Ring1][#Branch1][C][N][C][=Branch1][C][=O][C][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][=N][Ring1][#Branch1][C][=C][Ring2][Ring1][Ring2],\"7-chloro-5-[(4-methylphenyl)methyl]-2,3-dihydro-1,5-benzothiazepin-4-one\",3.7\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3c(C)n[nH]c3C)c2C(=O)N4C[C@H](O)CO4,\"InChI=1S/C21H27N5O5S/c1-10(2)7-25-20-17(18(28)24(5)21(25)30)16(19(29)26-8-13(27)9-31-26)15(32-20)6-14-11(3)22-23-12(14)4/h10,13,27H,6-9H2,1-5H3,(H,22,23)/t13-/m0/s1\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][=N][C][C][C][Branch1][C][C][=N][NH1][C][=Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][O][Ring1][=Branch1],\"6-[(3,5-dimethyl-1h-pyrazol-4-yl)methyl]-5-[(4s)-4-hydroxy1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[4,5-e]pyrimidine-2,4-dione\",1.07\nO=C1N(C(=Nc2c1cnn2c3ccccc3)c4occc4)c5ccccc5,InChI=1S/C21H14N4O2/c26-21-17-14-22-25(16-10-5-2-6-11-16)19(17)23-20(18-12-7-13-27-18)24(21)15-8-3-1-4-9-15/h1-14H,[O][=C][N][Branch2][Ring1][=C][C][=Branch2][Ring1][Ring1][=N][C][=C][Ring1][=Branch1][C][=N][N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][=C][C][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"6-furan-2-yl-1,5-di(phenyl)pyrazolo[4,5-e]pyrimidin-4-one\",3.29\nClc1ccc(OC2CCN(CC2)C3CCN(CC3)C(=O)C4=CNC(=O)c5ccccc45)cc1Cl,\"InChI=1S/C26H27Cl2N3O3/c27-23-6-5-19(15-24(23)28)34-18-9-13-30(14-10-18)17-7-11-31(12-8-17)26(33)22-16-29-25(32)21-4-2-1-3-20(21)22/h1-6,15-18H,7-14H2,(H,29,32)\",[Cl][C][=C][C][=C][Branch2][Ring2][O][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][S][Cl],\"4-[4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidine-1-carbonyl]-2h-isoquinolin-1-one\",3.51\nCOc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1,\"InChI=1S/C24H29N5O5/c1-32-18-3-5-20-19(12-18)29(23(31)15-34-20)11-10-28-8-6-16(7-9-28)25-13-17-2-4-21-24(26-17)27-22(30)14-33-21/h2-5,12,16,25H,6-11,13-15H2,1H3,(H,26,27,30)\",[C][O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S],\"6-[[[1-[2-(6-methoxy-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",0.87\nNc1ncnc2c1nc(Sc3nc4cccc(Cl)c4s3)n2CCO,\"InChI=1S/C14H11ClN6OS2/c15-7-2-1-3-8-10(7)23-14(19-8)24-13-20-9-11(16)17-6-18-12(9)21(13)4-5-22/h1-3,6,22H,4-5H2,(H2,16,17,18)\",[N][C][=N][C][=N][C][=C][Ring1][=Branch1][N][=C][Branch2][Ring1][C][S][C][=N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][S][Ring1][#Branch2][N][Ring1][S][C][C][O],\"2-[6-amino-8-[(7-chloro-1,3-benzothiazol-2-yl)sulfanyl]purin-9-yl]ethanol\",2.37\nCc1ccccc1C(=O)N2CCN(CC2)c3ccccn3,\"InChI=1S/C17H19N3O/c1-14-6-2-3-7-15(14)17(21)20-12-10-19(11-13-20)16-8-4-5-9-18-16/h2-9H,10-13H2,1H3\",[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1],(2-methylphenyl)-(4-pyridin-2-ylpiperazin-1-yl)methanone,2.18\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1C(C)C)NC(=O)OCc2ccccc2)C(=O)C(F)(F)F,\"InChI=1S/C23H27F3N4O5/c1-13(2)18(19(32)23(24,25)26)29-17(31)11-30-20(14(3)4)27-10-16(21(30)33)28-22(34)35-12-15-8-6-5-7-9-15/h5-10,13-14,18H,11-12H2,1-4H3,(H,28,34)(H,29,31)\",[C][C][Branch1][C][C][C][Branch2][Ring2][Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][O][=C][N][=C][Ring1][#Branch1][C][Branch1][C][C][C][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-propan-2-ylpyrimidin-5-yl]carbamate\",2.63\nCN(C)CCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1,\"InChI=1S/C22H25N7O2S/c1-28(2)14-5-12-25-32(30,31)18-9-7-17(8-10-18)26-22-23-13-11-19(27-22)20-16-24-21-6-3-4-15-29(20)21/h3-4,6-11,13,15-16,25H,5,12,14H2,1-2H3,(H,23,26,27)\",[C][N][Branch1][C][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"n-(3-dimethylaminopropyl)-4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\",1.9\nCOc1ccc(F)c(F)c1C(=O)c2cnc(NC3CCN(CC3)S(=O)(=O)C)nc2N,\"InChI=1S/C18H21F2N5O4S/c1-29-13-4-3-12(19)15(20)14(13)16(26)11-9-22-18(24-17(11)21)23-10-5-7-25(8-6-10)30(2,27)28/h3-4,9-10H,5-8H2,1-2H3,(H3,21,22,23,24)\",[C][O][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2][C][=Branch1][C][=O][C][=C][N][=C][Branch2][Ring1][Ring2][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][N][=C][Ring1][P][N],\"[4-amino-2-[(1-methylsulfonylpiperidin-4-yl)amino]pyrimidin-5-yl]-(2,3-difluoro-6-methoxyphenyl)methanone\",2.08\nClc1ccc(cc1)c2cn3ccccc3n2,InChI=1S/C13H9ClN2/c14-11-6-4-10(5-7-11)12-9-16-8-2-1-3-13(16)15-12/h1-9H,[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2],\"2-(4-chlorophenyl)imidazo[1,2-a]pyridine\",4\nCCN1C(=O)NC(C1=O)c2ccccc2,\"InChI=1S/C11H12N2O2/c1-2-13-10(14)9(12-11(13)15)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H,12,15)\",[C][C][N][C][=Branch1][C][=O][N][C][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-ethyl-5-phenylimidazolidine-2,4-dione\",1\nFC(F)(F)c1cc(CO[C@H]2CCCN[C@H]2c3ccccc3)cc(c1)C(F)(F)F,\"InChI=1S/C20H19F6NO/c21-19(22,23)15-9-13(10-16(11-15)20(24,25)26)12-28-17-7-4-8-27-18(17)14-5-2-1-3-6-14/h1-3,5-6,9-11,17-18,27H,4,7-8,12H2/t17-,18-/m0/s1\",[F][C][Branch1][C][F][Branch1][C][F][C][=C][C][Branch2][Ring1][Ring1][C][O][C@H1][C][C][C][N][C@H1][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][Ring2][C][Branch1][C][F][Branch1][C][F][F],\"(2s,3s)-3-[[3,5-bis(trifluoromethyl)phenyl]methoxy]-2-phenylpiperidine\",3.6\nCOC(=O)c1ccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)cc1,\"InChI=1S/C20H14ClN3O5/c1-29-20(28)11-4-2-10(3-5-11)9-24-19(27)15-16(18(26)23-24)22-14-8-12(21)6-7-13(14)17(15)25/h2-8H,9H2,1H3,(H,22,25)(H,23,26)\",[C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][=C][Ring2][Ring1][=Branch2],\"methyl 4-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]benzoate\",1.17\nCCN(CC)c1ncnc2c1ncn2Cc3c(Cl)cccc3Cl,\"InChI=1S/C16H17Cl2N5/c1-3-22(4-2)15-14-16(20-9-19-15)23(10-21-14)8-11-12(17)6-5-7-13(11)18/h5-7,9-10H,3-4,8H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][=N][C][=N][C][=C][Ring1][=Branch1][N][=C][N][Ring1][Branch1][C][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl],\"9-[(2,6-dichlorophenyl)methyl]-n,n-diethylpurin-6-amine\",1.25\nC[C@H](CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)cnc13,\"InChI=1S/C16H16F2N6OS/c1-8(6-25)21-14-13-15(22-11(19)5-20-13)24-16(23-14)26-7-9-3-2-4-10(17)12(9)18/h2-5,8,25H,6-7H2,1H3,(H3,19,21,22,23,24)/t8-/m1/s1\",[C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][=N][C][Branch1][C][N][=C][N][=C][Ring2][Ring1][Branch1][Ring1][#Branch1],\"(2r)-2-[[7-amino-2-[(2,3-difluorophenyl)methylsulfanyl]pteridin-4-yl]amino]propan-1-ol\",2.89\nOC(=O)c1ccc(Nc2ncc3CN=C(c4cc(Cl)ccc4c3n2)c5c(F)cccc5F)cc1,\"InChI=1S/C25H15ClF2N4O2/c26-15-6-9-17-18(10-15)23(21-19(27)2-1-3-20(21)28)29-11-14-12-30-25(32-22(14)17)31-16-7-4-13(5-8-16)24(33)34/h1-10,12H,11H2,(H,33,34)(H,30,31,32)\",[O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][=Branch2][N][C][=N][C][=C][C][N][=C][Branch2][Ring1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][Ring1][N][=N][Ring1][S][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][=C][Ring2][Ring1][#C],\"4-[[9-chloro-7-(2,6-difluorophenyl)-5h-pyrimido[5,4-d][2]benzazepin-2-yl]amino]benzoic acid\",2.58\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)N)C(=O)C(F)(F)F,\"InChI=1S/C19H20F3N3O3/c1-11(2)16(17(27)19(20,21)22)24-15(26)10-25-14(9-8-13(23)18(25)28)12-6-4-3-5-7-12/h3-9,11,16H,10,23H2,1-2H3,(H,24,26)\",[C][C][Branch1][C][C][C][Branch2][Ring1][=N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-(3-amino-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.74\nCc1cccc(NS(=O)(=O)c2cccc3nonc23)c1,\"InChI=1S/C13H11N3O3S/c1-9-4-2-5-10(8-9)16-20(17,18)12-7-3-6-11-13(12)15-19-14-11/h2-8,16H,1H3\",[C][C][=C][C][=C][C][Branch2][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=N][O][N][=C][Ring1][=Branch2][Ring1][Branch1][=C][Ring2][Ring1][Ring1],\"n-(3-methylphenyl)-2,1,3-benzoxadiazole-7-sulfonamide\",3\nO=S(=O)(Nc1ccccc1c2ccccc2)c3ccccc3,\"InChI=1S/C18H15NO2S/c20-22(21,16-11-5-2-6-12-16)19-18-14-8-7-13-17(18)15-9-3-1-4-10-15/h1-14,19H\",[O][=S][=Branch1][C][=O][Branch2][Ring1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-(2-phenylphenyl)benzenesulfonamide,3.96\nCC1=C(C)C(=O)C(=C(C)C1=O)C(CCCCCC(=O)O)c2ccccc2,\"InChI=1S/C22H26O4/c1-14-15(2)22(26)20(16(3)21(14)25)18(17-10-6-4-7-11-17)12-8-5-9-13-19(23)24/h4,6-7,10-11,18H,5,8-9,12-13H2,1-3H3,(H,23,24)\",[C][C][=C][Branch1][C][C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][Branch1][C][C][C][Ring1][=Branch2][=O][C][Branch1][O][C][C][C][C][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"7-phenyl-7-(2,4,5-trimethyl-3,6-dioxo-1-cyclohexa-1,4-dienyl)heptanoic acid\",2.48\nFc1ccc(cc1)C(NC(=O)CC2CCN(Cc3ccn(c3)c4ccc(cc4)C(F)(F)F)CC2)C5=CNC(=O)C=C5,\"InChI=1S/C31H30F4N4O2/c32-26-6-1-23(2-7-26)30(24-3-10-28(40)36-18-24)37-29(41)17-21-11-14-38(15-12-21)19-22-13-16-39(20-22)27-8-4-25(5-9-27)31(33,34)35/h1-10,13,16,18,20-21,30H,11-12,14-15,17,19H2,(H,36,40)(H,37,41)\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch2][Ring2][#C][N][C][=Branch1][C][=O][C][C][C][C][N][Branch2][Ring1][=N][C][C][C][=C][N][Branch1][Ring2][C][=Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][C][Ring2][Ring1][=Branch1][C][=C][N][C][=Branch1][C][=O][C][=C][Ring1][#Branch1],n-[(4-fluorophenyl)-(6-oxo-1h-pyridin-3-yl)methyl]-2-[1-[[1-[4-(trifluoromethyl)phenyl]pyrrol-3-yl]methyl]piperidin-4-yl]acetamide,3.04\nCC(N1NC(=O)C2=C(C1=O)C(=O)c3ccc(Cl)cc3N2)c4oc5ccccc5c4,\"InChI=1S/C21H14ClN3O4/c1-10(16-8-11-4-2-3-5-15(11)29-16)25-21(28)17-18(20(27)24-25)23-14-9-12(22)6-7-13(14)19(17)26/h2-10H,1H3,(H,23,26)(H,24,27)\",[C][C][Branch2][Ring1][P][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2],\"2-[1-(1-benzofuran-2-yl)ethyl]-7-chloro-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",2.1\nCCCC(=O)Nc1ccc2c3ccccc3C(=O)C(=O)c2c1,\"InChI=1S/C18H15NO3/c1-2-5-16(20)19-11-8-9-13-12-6-3-4-7-14(12)17(21)18(22)15(13)10-11/h3-4,6-10H,2,5H2,1H3,(H,19,20)\",[C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][Ring1][N][=C][Ring1][S],\"n-(9,10-dioxophenanthren-2-yl)butanamide\",2.81\nCC(C)(O)c1ccccc1CC[C@@H](SCC2(CC(=O)O)CC2)c3cccc(\\C=C\\c4ccc5ccc(Cl)cc5n4)c3,\"InChI=1S/C35H36ClNO3S/c1-34(2,40)30-9-4-3-7-25(30)13-17-32(41-23-35(18-19-35)22-33(38)39)27-8-5-6-24(20-27)10-15-29-16-12-26-11-14-28(36)21-31(26)37-29/h3-12,14-16,20-21,32,40H,13,17-19,22-23H2,1-2H3,(H,38,39)/b15-10+/t32-/m1/s1\",[C][C][Branch1][C][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C@@H1][Branch1][S][S][C][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][C][Ring1][#Branch1][C][=C][C][=C][C][Branch2][Ring1][Ring2][\\C][=C][\\C][=C][C][=C][C][=C][C][Branch1][C][Cl][=C][C][Ring1][#Branch1][=N][Ring1][O][=C][Ring2][Ring1][Ring1],\"2-[1-[[(1r)-1-[3-[(e)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl]-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl]sulfanylmethyl]cyclopropyl]acetic acid\n2-[1-[[(1r)-1-[3-[2-(7-chloroquinolin-2-yl)ethenyl]phenyl]-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl]sulfanylmethyl]cyclopropyl]acetic acid\",3.45\nClc1ccc(Nc2nnc(Cc3ccncc3)c4ccccc24)cc1,\"InChI=1S/C20H15ClN4/c21-15-5-7-16(8-6-15)23-20-18-4-2-1-3-17(18)19(24-25-20)13-14-9-11-22-12-10-14/h1-12H,13H2,(H,23,25)\",[Cl][C][=C][C][=C][Branch2][Ring1][O][N][C][=N][N][=C][Branch1][#Branch2][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch2],n-(4-chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine,3.7\nNc1ccc(cc1)S(=O)(=O)c2ccc(N)cc2,\"InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2\",[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],4-(4-aminophenyl)sulfonylaniline,0.88\nCOc1ccc2nccc([C@H](O)[C@H]3C[C@@H]4CCN3C[C@@H]4C=C)c2c1,\"InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14-,19+,20-/m0/s1\",[C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Ring1][C@H1][Branch1][C][O][C@H1][C][C@@H1][C][C][N][Ring1][=Branch1][C][C@@H1][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1],\"(s)-[(4s,5r,7r)-5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl]-(6-methoxyquinolin-4-yl)methanol\",2.21\nNC(=O)Cc1ccccc1,\"InChI=1S/C8H9NO/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)\",[N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-phenylacetamide,0.3\nCC(=O)O[C@H]1CC[C@]2(C=O)[C@H]3CC[C@]4(C)[C@H](CC[C@]4(O)[C@@H]3CC[C@]2(O)C1)C5=CC(=O)OC5,\"InChI=1S/C25H34O7/c1-15(27)32-17-3-8-23(14-26)19-4-7-22(2)18(16-11-21(28)31-13-16)6-10-25(22,30)20(19)5-9-24(23,29)12-17/h11,14,17-20,29-30H,3-10,12-13H2,1-2H3/t17-,18+,19-,20+,22+,23-,24-,25-/m0/s1\",[C][C][=Branch1][C][=O][O][C@H1][C][C][C@][Branch1][Ring1][C][=O][C@H1][C][C][C@][Branch1][C][C][C@H1][Branch2][Ring1][Branch2][C][C][C@][Ring1][=Branch1][Branch1][C][O][C@@H1][Ring1][O][C][C][C@][Ring1][P][Branch1][C][O][C][Ring2][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][O][C][Ring1][=Branch1],\"[(3s,5s,8r,9s,10s,13r,14s,17r)-10-formyl-5,14-dihydroxy-13-methyl-17-(5-oxo-2h-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] acetate\",0.64\nCOc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN4CCC[C@H]4C(=O)N,\"InChI=1S/C21H21ClFN5O2/c1-30-18-9-16-13(8-12(18)10-28-7-3-6-17(28)20(24)29)21(26-11-25-16)27-15-5-2-4-14(22)19(15)23/h2,4-5,8-9,11,17H,3,6-7,10H2,1H3,(H2,24,29)(H,25,26,27)/t17-/m0/s1\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][C][C][C][C@H1][Ring1][Branch1][C][=Branch1][C][=O][N],(2s)-1-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl]pyrrolidine-2-carboxamide,3.58\nCC(C)NNC(=O)c1ccncc1,\"InChI=1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13)\",[C][C][Branch1][C][C][N][N][C][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1],n'-propan-2-ylpyridine-4-carbohydrazide,0.33\nNC(=O)Nc1sc(cc1C(=O)N)c2ccccc2,\"InChI=1S/C12H11N3O2S/c13-10(16)8-6-9(7-4-2-1-3-5-7)18-11(8)15-12(14)17/h1-6H,(H2,13,16)(H3,14,15,17)\",[N][C][=Branch1][C][=O][N][C][S][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(carbamoylamino)-5-phenylthiophene-3-carboxamide,2.42\nNc1ccc(N=Nc2ccccc2)c(N)n1,\"InChI=1S/C11H11N5/c12-10-7-6-9(11(13)14-10)16-15-8-4-2-1-3-5-8/h1-7H,(H4,12,13,14)\",[N][C][=C][C][=C][Branch1][O][N][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][N][=N][Ring1][#C],\"3-phenyldiazenylpyridine-2,6-diamine\",3.22\nCc1ccc(cc1)N2NC(=O)c3cccnc23,\"InChI=1S/C13H11N3O/c1-9-4-6-10(7-5-9)16-12-11(13(17)15-16)3-2-8-14-12/h2-8H,1H3,(H,15,17)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1],\"1-(4-methylphenyl)-2h-pyrazolo[5,4-b]pyridin-3-one\",2.1\nCOc1ccc(cc1)C(=O)N2CCCC2=O,\"InChI=1S/C12H13NO3/c1-16-10-6-4-9(5-7-10)12(15)13-8-2-3-11(13)14/h4-7H,2-3,8H2,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=O],1-(4-methoxybenzoyl)pyrrolidin-2-one,0.93\nClc1cccc2[nH]ncc12,\"InChI=1S/C7H5ClN2/c8-6-2-1-3-7-5(6)4-9-10-7/h1-4H,(H,9,10)\",[Cl][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1],4-chloro-1h-indazole,2.5\nNc1ccc(Cl)c(c1)c2oc3cccnc3n2,\"InChI=1S/C12H8ClN3O/c13-9-4-3-7(14)6-8(9)12-16-11-10(17-12)2-1-5-15-11/h1-6H,14H2\",[N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][=Ring1][=Branch2],\"4-chloro-3-([1,3]oxazolo[4,5-b]pyridin-2-yl)aniline\",1.97\nC[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc3ccc(Cl)cc3NC(=O)N,\"InChI=1S/C21H24ClFN4O3/c1-14-11-26(12-15-2-5-17(23)6-3-15)8-9-27(14)20(28)13-30-19-7-4-16(22)10-18(19)25-21(24)29/h2-7,10,14H,8-9,11-13H2,1H3,(H3,24,25,29)/t14-/m1/s1\",[C][C@@H1][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][N][Ring1][=C][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][N],[5-chloro-2-[2-[(2r)-4-[(4-fluorophenyl)methyl]-2-methylpiperazin-1-yl]-2-oxoethoxy]phenyl]urea,1.91\nCN(C1CCN(CCC(c2ccccc2)c3ccccc3)CC1)C(=O)c4ccncc4,\"InChI=1S/C27H31N3O/c1-29(27(31)24-12-17-28-18-13-24)25-14-19-30(20-15-25)21-16-26(22-8-4-2-5-9-22)23-10-6-3-7-11-23/h2-13,17-18,25-26H,14-16,19-21H2,1H3\",[C][N][Branch2][Ring2][C][C][C][C][N][Branch2][Ring1][=Branch1][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1],\"n-[1-[3,3-di(phenyl)propyl]piperidin-4-yl]-n-methylpyridine-4-carboxamide\",2.8\nCc1ccc(cc1)C(=O)Oc2ccc(cc2OC(=O)c3ccc(C)cc3)C(O)CNC(C)(C)C,\"InChI=1S/C28H31NO5/c1-18-6-10-20(11-7-18)26(31)33-24-15-14-22(23(30)17-29-28(3,4)5)16-25(24)34-27(32)21-12-8-19(2)9-13-21/h6-16,23,29-30H,17H2,1-5H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch2][Ring1][Branch1][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][Branch1][C][O][C][N][C][Branch1][C][C][Branch1][C][C][C],[5-[2-(tert-butylamino)-1-hydroxyethyl]-2-(4-methylbenzoyl)oxyphenyl] 4-methylbenzoate,3.57\nCCCCC(CC)CNC(=O)c1ccc2c(c1)c(Cc3ccc(cc3OC)C(=O)NS(=O)(=O)c4ccccc4C)cn2C,\"InChI=1S/C34H41N3O5S/c1-6-8-12-24(7-2)21-35-33(38)26-16-17-30-29(19-26)28(22-37(30)4)18-25-14-15-27(20-31(25)42-5)34(39)36-43(40,41)32-13-10-9-11-23(32)3/h9-11,13-17,19-20,22,24H,6-8,12,18,21H2,1-5H3,(H,35,38)(H,36,39)\",[C][C][C][C][C][Branch1][Ring1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch2][Ring2][Ring1][C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][N][Ring2][Ring1][N][C],n-(2-ethylhexyl)-3-[[2-methoxy-4-[(2-methylphenyl)sulfonylcarbamoyl]phenyl]methyl]-1-methylindole-5-carboxamide,3.66\nCCN(C1CCN(CCC(c2ccccc2)c3ccc(cc3)S(=O)(=O)C)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H40N2O5S2/c1-4-34(32(35)24-25-10-14-29(15-11-25)40(2,36)37)28-18-21-33(22-19-28)23-20-31(26-8-6-5-7-9-26)27-12-16-30(17-13-27)41(3,38)39/h5-17,28,31H,4,18-24H2,1-3H3\",[C][C][N][Branch2][Ring2][N][C][C][C][N][Branch2][Ring1][S][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring2][Ring1][=Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[3-(4-methylsulfonylphenyl)-3-phenylpropyl]piperidin-4-yl]acetamide,1.73\nCOCCOc1nc(N)c2NC(=O)N(Cc3ccccc3)c2n1,\"InChI=1S/C15H17N5O3/c1-22-7-8-23-14-18-12(16)11-13(19-14)20(15(21)17-11)9-10-5-3-2-4-6-10/h2-6H,7-9H2,1H3,(H,17,21)(H2,16,18,19)\",[C][O][C][C][O][C][=N][C][Branch1][C][N][=C][N][C][=Branch1][C][=O][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=N][=N][Ring2][Ring1][C],6-amino-2-(2-methoxyethoxy)-9-(phenylmethyl)-7h-purin-8-one,2.26\nCOc1ccc(CC(C)(C)NC[C@H](O)c2cc(O)cc3NC(=O)COc23)cc1,\"InChI=1S/C21H26N2O5/c1-21(2,10-13-4-6-15(27-3)7-5-13)22-11-18(25)16-8-14(24)9-17-20(16)28-12-19(26)23-17/h4-9,18,22,24-25H,10-12H2,1-3H3,(H,23,26)/t18-/m0/s1\",[C][O][C][=C][C][=C][Branch2][Ring2][Ring1][C][C][Branch1][C][C][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][Branch1][C][O][=C][C][N][C][=Branch1][C][=O][C][O][C][Ring1][N][=Ring1][#Branch1][C][=C][Ring2][Ring1][#Branch2],\"6-hydroxy-8-[(1r)-1-hydroxy-2-[[1-(4-methoxyphenyl)-2-methylpropan-2-yl]amino]ethyl]-4h-1,4-benzoxazin-3-one\",0.79\nCC1=CC(=O)Nc2ccccc12,\"InChI=1S/C10H9NO/c1-7-6-10(12)11-9-5-3-2-4-8(7)9/h2-6H,1H3,(H,11,12)\",[C][C][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1],4-methyl-1h-quinolin-2-one,1.9\nC[C@H](Cc1cccc(CC(=O)NC23CC4CC(CC(C4)C2)C3)c1)NC[C@H](O)c5ccc(O)c(CO)c5,\"InChI=1S/C30H40N2O4/c1-19(31-17-28(35)25-5-6-27(34)26(13-25)18-33)7-20-3-2-4-21(8-20)12-29(36)32-30-14-22-9-23(15-30)11-24(10-22)16-30/h2-6,8,13,19,22-24,28,31,33-35H,7,9-12,14-18H2,1H3,(H,32,36)/t19-,22?,23?,24?,28+,30?/m1/s1\",[C][C@H1][Branch2][Ring2][Branch2][C][C][=C][C][=C][C][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][Branch1][Ring1][C][O][=C][Ring1][=Branch2],n-(1-adamantyl)-2-[3-[(2r)-2-[[(2r)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl]amino]propyl]phenyl]acetamide,2.4\nOc1ccc(cc1)c2ccc(cc2)C3(O)CN4CCC3CC4,\"InChI=1S/C19H21NO2/c21-18-7-3-15(4-8-18)14-1-5-16(6-2-14)19(22)13-20-11-9-17(19)10-12-20/h1-8,17,21-22H,9-13H2\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][N][C][C][C][Ring1][#Branch1][C][C][Ring1][=Branch1],8-[4-(4-hydroxyphenyl)phenyl]-1-azabicyclo[2.2.2]octan-8-ol,0.95\nCNC(=O)c1snnc1c2ccccc2,\"InChI=1S/C10H9N3OS/c1-11-10(14)9-8(12-13-15-9)7-5-3-2-4-6-7/h2-6H,1H3,(H,11,14)\",[C][N][C][=Branch1][C][=O][C][S][N][=N][C][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-methyl-4-phenylthiadiazole-5-carboxamide,1.23\nCC(C)(C)NC(=O)Nc1cccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)c1,\"InChI=1S/C23H22ClN5O4/c1-23(2,3)27-22(33)25-14-6-4-5-12(9-14)11-29-21(32)17-18(20(31)28-29)26-16-10-13(24)7-8-15(16)19(17)30/h4-10H,11H2,1-3H3,(H,26,30)(H,28,31)(H2,25,27,33)\",[C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][=C][Ring2][Ring1][=Branch2],\"1-tert-butyl-3-[3-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]phenyl]urea\",1.77\nCN1CCN(CC1)c2nc(NCCNc3ccc(cc3)[N+](=O)[O-])c4ccccc4n2,\"InChI=1S/C21H25N7O2/c1-26-12-14-27(15-13-26)21-24-19-5-3-2-4-18(19)20(25-21)23-11-10-22-16-6-8-17(9-7-16)28(29)30/h2-9,22H,10-15H2,1H3,(H,23,24,25)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][Ring2][N][C][C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring2][Ring1][#Branch1],\"n-[2-(4-methylpiperazin-1-yl)quinazolin-4-yl]-n'-(4-nitrophenyl)ethane-1,2-diamine\",2.91\nCC(C)CN1C(=O)NC(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CCC4,\"InChI=1S/C22H22F3N3O3S/c1-12(2)11-28-20-17(18(29)26-21(28)31)16(19(30)27-8-5-9-27)15(32-20)10-13-6-3-4-7-14(13)22(23,24)25/h3-4,6-7,12H,5,8-11H2,1-2H3,(H,26,29,31)\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][=C][Ring1][Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring2],\"5-(azetidine-1-carbonyl)-1-(2-methylpropyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\",3\nO=C(COCc1ccccc1)Nc2ccc3c(c2)C(=O)C(=O)c4ccccc34,\"InChI=1S/C23H17NO4/c25-21(14-28-13-15-6-2-1-3-7-15)24-16-10-11-18-17-8-4-5-9-19(17)22(26)23(27)20(18)12-16/h1-12H,13-14H2,(H,24,25)\",[O][=C][Branch1][N][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"n-(9,10-dioxophenanthren-2-yl)-2-(phenylmethoxy)acetamide\",3.21\nCNS(=O)(=O)Cc1ccc2[nH]cc(CCN(C)C)c2c1,\"InChI=1S/C14H21N3O2S/c1-15-20(18,19)10-11-4-5-14-13(8-11)12(9-16-14)6-7-17(2)3/h4-5,8-9,15-16H,6-7,10H2,1-3H3\",[C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][NH1][C][=C][Branch1][Branch2][C][C][N][Branch1][C][C][C][C][Ring1][#Branch2][=C][Ring1][=C],1-[3-(2-dimethylaminoethyl)-1h-indol-5-yl]-n-methylmethanesulfonamide,-0.96\nCC(C)(CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)sc13,\"InChI=1S/C16H17F2N5OS2/c1-16(2,7-24)23-13-11-12(20-14(19)26-11)21-15(22-13)25-6-8-4-3-5-9(17)10(8)18/h3-5,24H,6-7H2,1-2H3,(H3,19,20,21,22,23)\",[C][C][Branch1][C][C][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1],\"2-[[2-amino-5-[(2,3-difluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]-2-methylpropan-1-ol\",3.37\nOc1cc(O)c2C(=O)C=C(Oc2c1)c3ccccc3,\"InChI=1S/C15H10O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-8,16-17H\",[O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5,7-dihydroxy-2-phenylchromen-4-one\",3.83\nO=C(Nc1ccccn1)c2ccccc2,\"InChI=1S/C12H10N2O/c15-12(10-6-2-1-3-7-10)14-11-8-4-5-9-13-11/h1-9H,(H,13,14,15)\",[O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-pyridin-2-ylbenzamide,2.2\nON1C(=O)N(CC2COc3ccccc3O2)c4ccsc4C1=O,\"InChI=1S/C15H12N2O5S/c18-14-13-10(5-6-23-13)16(15(19)17(14)20)7-9-8-21-11-3-1-2-4-12(11)22-9/h1-6,9,20H,7-8H2\",[O][N][C][=Branch1][C][=O][N][Branch1][S][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][Ring1][#Branch2][C][C][=C][S][C][=Ring1][Branch1][C][Ring2][Ring1][Branch1][=O],\"1-(2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-3-hydroxythieno[2,3-e]pyrimidine-2,4-dione\",1.44\nS(c1ccccc1)c2ccc3ccccc3n2,InChI=1S/C15H11NS/c1-2-7-13(8-3-1)17-15-11-10-12-6-4-5-9-14(12)16-15/h1-11H,[S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2],2-phenylsulfanylquinoline,3.92\nCOCCOCCOc1ccc(cc1)c2cc(C(=O)N)c(NC(=O)N)s2,\"InChI=1S/C17H21N3O5S/c1-23-6-7-24-8-9-25-12-4-2-11(3-5-12)14-10-13(15(18)21)16(26-14)20-17(19)22/h2-5,10H,6-9H2,1H3,(H2,18,21)(H3,19,20,22)\",[C][O][C][C][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][N][S][Ring1][N],2-(carbamoylamino)-5-[4-[2-(2-methoxyethoxy)ethoxy]phenyl]thiophene-3-carboxamide,2.21\nCCc1nc(N)nc(N)c1c2ccc(Cl)cc2,\"InChI=1S/C12H13ClN4/c1-2-9-10(11(14)17-12(15)16-9)7-3-5-8(13)6-4-7/h3-6H,2H2,1H3,(H4,14,15,16,17)\",[C][C][C][=N][C][Branch1][C][N][=N][C][Branch1][C][N][=C][Ring1][Branch2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine\",2.31\nC[C@@H](C(=O)NCCN1CCCC1)c2ccc(OS(=O)(=O)C(F)(F)F)cc2,\"InChI=1S/C16H21F3N2O4S/c1-12(15(22)20-8-11-21-9-2-3-10-21)13-4-6-14(7-5-13)25-26(23,24)16(17,18)19/h4-7,12H,2-3,8-11H2,1H3,(H,20,22)/t12-/m1/s1\",[C][C@@H1][Branch1][#C][C][=Branch1][C][=O][N][C][C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][Branch1][P][O][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][=C],[4-[(2r)-1-oxo-1-(2-pyrrolidin-1-ylethylamino)propan-2-yl]phenyl] trifluoromethanesulfonate,1.64\nNc1ccc(OCCc2ccccc2)cc1,\"InChI=1S/C14H15NO/c15-13-6-8-14(9-7-13)16-11-10-12-4-2-1-3-5-12/h1-9H,10-11,15H2\",[N][C][=C][C][=C][Branch1][N][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#C],4-(2-phenylethoxy)aniline,2.71\nFc1cnc(NC(=O)C(CC2CCOCC2)c3ccc(cc3)S(=O)(=O)C4CC4)s1,\"InChI=1S/C20H23FN2O4S2/c21-18-12-22-20(28-18)23-19(24)17(11-13-7-9-27-10-8-13)14-1-3-15(4-2-14)29(25,26)16-5-6-16/h1-4,12-13,16-17H,5-11H2,(H,22,23,24)\",[F][C][=C][N][=C][Branch2][Ring2][Branch2][N][C][=Branch1][C][=O][C][Branch1][#Branch2][C][C][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring1][Ring1][S][Ring2][Ring1][N],\"2-(4-cyclopropylsulfonylphenyl)-n-(5-fluoro-1,3-thiazol-2-yl)-3-(oxan-4-yl)propanamide\",3.3\nCC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)C(=O)NC4CCN(C)CC4)ncc2F,\"InChI=1S/C24H30FN7O/c1-15(2)32-16(3)26-14-21(32)22-20(25)13-27-24(30-22)29-18-7-5-17(6-8-18)23(33)28-19-9-11-31(4)12-10-19/h5-8,13-15,19H,9-12H2,1-4H3,(H,28,33)(H,27,29,30)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=N][C][=C][Ring2][Ring1][#Branch1][F],4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-(1-methylpiperidin-4-yl)benzamide,2.13\nOc1ccc2OC(=CC(=O)c2c1)c3ccccc3,\"InChI=1S/C15H10O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-9,16H\",[O][C][=C][C][=C][O][C][=Branch1][N][=C][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][C][=C][Ring1][=Branch1],6-hydroxy-2-phenylchromen-4-one,3.6\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccs2)NC(=O)OCC(F)(F)F)C(=O)C(F)(F)F,\"InChI=1S/C19H18F6N4O5S/c1-9(2)13(14(31)19(23,24)25)28-12(30)7-29-15(11-4-3-5-35-11)26-6-10(16(29)32)27-17(33)34-8-18(20,21)22/h3-6,9,13H,7-8H2,1-2H3,(H,27,33)(H,28,30)\",[C][C][Branch1][C][C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=N][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1][N][C][=Branch1][C][=O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2,2,2-trifluoroethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-thiophen-2-ylpyrimidin-5-yl]carbamate\",2.32\nNS(=O)(=O)c1ccc(Nc2nccc(n2)c3ccccc3)cc1,\"InChI=1S/C16H14N4O2S/c17-23(21,22)14-8-6-13(7-9-14)19-16-18-11-10-15(20-16)12-4-2-1-3-5-12/h1-11H,(H2,17,21,22)(H,18,19,20)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Ring2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1],4-[(4-phenylpyrimidin-2-yl)amino]benzenesulfonamide,2.86\nCC(C)[N+](C)(CCOC(=O)C1c2ccccc2Oc3ccccc13)C(C)C,\"InChI=1S/C23H30NO3/c1-16(2)24(5,17(3)4)14-15-26-23(25)22-18-10-6-8-12-20(18)27-21-13-9-7-11-19(21)22/h6-13,16-17,22H,14-15H2,1-5H3/q+1\",[C][C][Branch1][C][C][N+1][Branch1][C][C][Branch2][Ring1][N][C][C][O][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][C][C],methyl-di(propan-2-yl)-[2-(9h-xanthene-9-carbonyloxy)ethyl]azanium,0.2\nCC1CC(NC(=O)C)c2ccccc2N1C(=O)c3ccccc3,\"InChI=1S/C19H20N2O2/c1-13-12-17(20-14(2)22)16-10-6-7-11-18(16)21(13)19(23)15-8-4-3-5-9-15/h3-11,13,17H,12H2,1-2H3,(H,20,22)\",[C][C][C][C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-[1-(benzoyl)-2-methyl-3,4-dihydro-2h-quinolin-4-yl]acetamide\",2\nOCC(O)CN1CCN(CC1)c2ccccc2,\"InChI=1S/C13H20N2O2/c16-11-13(17)10-14-6-8-15(9-7-14)12-4-2-1-3-5-12/h1-5,13,16-17H,6-11H2\",[O][C][C][Branch1][C][O][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-(4-phenylpiperazin-1-yl)propane-1,2-diol\",0.4\nC[C@@H](CO)Oc1cc(Oc2ccc(cc2)S(=O)(=O)C)cc(c1)C(=O)Nc3nccs3,\"InChI=1S/C20H20N2O6S2/c1-13(12-23)27-16-9-14(19(24)22-20-21-7-8-29-20)10-17(11-16)28-15-3-5-18(6-4-15)30(2,25)26/h3-11,13,23H,12H2,1-2H3,(H,21,22,24)/t13-/m0/s1\",[C][C@@H1][Branch1][Ring1][C][O][O][C][=C][C][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][Ring2][=C][Ring1][P][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"3-[(2s)-1-hydroxypropan-2-yl]oxy-5-(4-methylsulfonylphenoxy)-n-(1,3-thiazol-2-yl)benzamide\",2.63\nCc1sc2ncnc(N3CCN(CC3)c4ncccn4)c2c1C,\"InChI=1S/C16H18N6S/c1-11-12(2)23-15-13(11)14(19-10-20-15)21-6-8-22(9-7-21)16-17-4-3-5-18-16/h3-5,10H,6-9H2,1-2H3\",[C][C][S][C][=N][C][=N][C][Branch2][Ring1][Ring1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=N][Ring1][=Branch1][=C][Ring2][Ring1][C][C][=Ring2][Ring1][Branch1][C],\"5,6-dimethyl-4-(4-pyrimidin-2-ylpiperazin-1-yl)thieno[2,3-d]pyrimidine\",3.66\nCN1CC(c2ccc(Cl)cc2)c3ccccc3C1,\"InChI=1S/C16H16ClN/c1-18-10-13-4-2-3-5-15(13)16(11-18)12-6-8-14(17)9-7-12/h2-9,16H,10-11H2,1H3\",[C][N][C][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][P],\"4-(4-chlorophenyl)-2-methyl-3,4-dihydro-1h-isoquinoline\",3.64\nOC(=O)CSc1c[nH]c2ccccc12,\"InChI=1S/C10H9NO2S/c12-10(13)6-14-9-5-11-8-4-2-1-3-7(8)9/h1-5,11H,6H2,(H,12,13)\",[O][C][=Branch1][C][=O][C][S][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1],2-(1h-indol-3-ylsulfanyl)acetic acid,-1.31\nCc1nnc2CN=C(c3ccccc3)c4cc(Cl)ccc4n12,\"InChI=1S/C17H13ClN4/c1-11-20-21-16-10-19-17(12-5-3-2-4-6-12)14-9-13(18)7-8-15(14)22(11)16/h2-9H,10H2,1H3\",[C][C][=N][N][=C][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][Branch1][Ring2][Ring1][C],\"8-chloro-1-methyl-6-phenyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine\",1.98\nCS(=O)(=O)c1cccc(Nc2nccc(Nc3cccc4[nH]ncc34)n2)c1,\"InChI=1S/C18H16N6O2S/c1-27(25,26)13-5-2-4-12(10-13)21-18-19-9-8-17(23-18)22-15-6-3-7-16-14(15)11-20-24-16/h2-11H,1H3,(H,20,24)(H2,19,21,22,23)\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring1][#Branch2][N][C][=N][C][=C][C][Branch1][#C][N][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1][=N][Ring1][S][=C][Ring2][Ring1][#Branch1],\"n'-(1h-indazol-4-yl)-n-(3-methylsulfonylphenyl)pyrimidine-2,4-diamine\",2.91\nOc1c(NC(=O)Nc2cccc(F)c2Cl)ccc(Cl)c1S(=O)(=O)N3CCNCC3,\"InChI=1S/C17H17Cl2FN4O4S/c18-10-4-5-13(23-17(26)22-12-3-1-2-11(20)14(12)19)15(25)16(10)29(27,28)24-8-6-21-7-9-24/h1-5,21,25H,6-9H2,(H2,22,23,26)\",[O][C][=C][Branch2][Ring1][Ring1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][Ring2][Ring1][Ring1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][C][C][Ring1][=Branch1],3-(2-chloro-3-fluorophenyl)-1-(4-chloro-2-hydroxy-3-piperazin-1-ylsulfonylphenyl)urea,2.6\nCN1CCC(=CC1)c2cccc(O)c2,\"InChI=1S/C12H15NO/c1-13-7-5-10(6-8-13)11-3-2-4-12(14)9-11/h2-5,9,14H,6-8H2,1H3\",[C][N][C][C][C][=Branch1][Branch1][=C][C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1],\"3-(1-methyl-3,6-dihydro-2h-pyridin-4-yl)phenol\",0.53\nOC(=O)COc1ccc(C(=O)c2cccs2)c(Cl)c1Cl,\"InChI=1S/C13H8Cl2O4S/c14-11-7(13(18)9-2-1-5-20-9)3-4-8(12(11)15)19-6-10(16)17/h1-5H,6H2,(H,16,17)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][S][Ring1][Branch1][C][Branch1][C][Cl][=C][Ring1][=C][Cl],\"2-[2,3-dichloro-4-(thiophene-2-carbonyl)phenoxy]acetic acid\",-0.84\nCOCC1=C(N2[C@H](SC1)[C@H](NC(=O)\\C(=N/OC)\\c3csc(N)n3)C2=O)C(=O)OC(C)OC(=O)OC(C)C,\"InChI=1S/C21H27N5O9S2/c1-9(2)33-21(30)35-10(3)34-19(29)15-11(6-31-4)7-36-18-14(17(28)26(15)18)24-16(27)13(25-32-5)12-8-37-20(22)23-12/h8-10,14,18H,6-7H2,1-5H3,(H2,22,23)(H,24,27)/b25-13-/t10?,14-,18-/m1/s1\",[C][O][C][C][=C][Branch2][Ring2][#Branch1][N][C@H1][Branch1][Branch1][S][C][Ring1][=Branch1][C@H1][Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][\\C][=Branch1][Ring2][=N][/O][C][\\C][=C][S][C][Branch1][C][N][=N][Ring1][=Branch1][C][Ring2][Ring1][Ring1][=O][C][=Branch1][C][=O][O][C][Branch1][C][C][O][C][=Branch1][C][=O][O][C][Branch1][C][C][C],\"1-propan-2-yloxycarbonyloxyethyl (6r,7r)-7-[[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate\",1.7\nOCCN(CCO)c1nc(N2CCCCC2)c3nc(nc(N4CCCCC4)c3n1)N(CCO)CCO,\"InChI=1S/C24H40N8O4/c33-15-11-31(12-16-34)23-26-20-19(21(27-23)29-7-3-1-4-8-29)25-24(32(13-17-35)14-18-36)28-22(20)30-9-5-2-6-10-30/h33-36H,1-18H2\",[O][C][C][N][Branch1][Ring2][C][C][O][C][=N][C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1][=C][N][=C][Branch2][Ring1][Ring2][N][=C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1][C][Ring1][N][=N][Ring2][Ring1][=Branch1][N][Branch1][Ring2][C][C][O][C][C][O],\"2-[[2-(bis(2-hydroxyethyl)amino)-4,8-di(piperidin-1-yl)pyrimido[6,5-e]pyrimidin-6-yl]-(2-hydroxyethyl)amino]ethanol\",3.97\nCCN(CC)CCOC(=O)C1(CCCCC1)C2CCCCC2,\"InChI=1S/C19H35NO2/c1-3-20(4-2)15-16-22-18(21)19(13-9-6-10-14-19)17-11-7-5-8-12-17/h17H,3-16H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][C][O][C][=Branch1][C][=O][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][C][C][Ring1][=Branch1],2-diethylaminoethyl 1-cyclohexylcyclohexane-1-carboxylate,3.72\nCc1nc2ccccn2c1c3ccnc(Nc4cccc(Cl)c4)n3,\"InChI=1S/C18H14ClN5/c1-12-17(24-10-3-2-7-16(24)21-12)15-8-9-20-18(23-15)22-14-6-4-5-13(19)11-14/h2-11H,1H3,(H,20,22,23)\",[C][C][N][=C][C][=C][C][=C][N][Ring1][=Branch1][C][=Ring1][=Branch2][C][=C][C][=N][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=N][Ring1][=C],\"n-(3-chlorophenyl)-4-(2-methylimidazo[3,2-a]pyridin-3-yl)pyrimidin-2-amine\",2.7\nCN(C)c1cccc(c1)C(=O)Nc2ccc(C)c(NC(=O)c3ccc(O)cc3)c2,\"InChI=1S/C23H23N3O3/c1-15-7-10-18(24-23(29)17-5-4-6-19(13-17)26(2)3)14-21(15)25-22(28)16-8-11-20(27)12-9-16/h4-14,27H,1-3H3,(H,24,29)(H,25,28)\",[C][N][Branch1][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][=C][Ring1][P],3-dimethylamino-n-[3-[(4-hydroxybenzoyl)amino]-4-methylphenyl]benzamide,2.65\nCc1cccc(Nc2ncnc3ccc(NC(=O)C=C)cc23)c1,\"InChI=1S/C18H16N4O/c1-3-17(23)21-14-7-8-16-15(10-14)18(20-11-19-16)22-13-6-4-5-12(2)9-13/h3-11H,1H2,2H3,(H,21,23)(H,19,20,22)\",[C][C][=C][C][=C][C][Branch2][Ring1][=Branch2][N][C][=N][C][=N][C][=C][C][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][#C][Ring1][O][=C][Ring2][Ring1][=Branch1],n-[4-[(3-methylphenyl)amino]quinazolin-6-yl]prop-2-enamide,3.7\nCOc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC,\"InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3\",[C][O][C][=C][C][C][C][Branch2][Ring1][Branch1][C][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring1][=N][C][=Branch1][C][=O][C][=Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][Branch2][O][C],\"5,6-dimethoxy-2-[[1-(phenylmethyl)piperidin-4-yl]methyl]-2,3-dihydroinden-1-one\",2.41\nCc1cnc(Nc2ccc(OCCN3CCCC3)cc2)nc1Nc4cccc(c4)S(=O)(=O)NC(C)(C)C,\"InChI=1S/C27H36N6O3S/c1-20-19-28-26(30-21-10-12-23(13-11-21)36-17-16-33-14-5-6-15-33)31-25(20)29-22-8-7-9-24(18-22)37(34,35)32-27(2,3)4/h7-13,18-19,32H,5-6,14-17H2,1-4H3,(H2,28,29,30,31)\",[C][C][=C][N][=C][Branch2][Ring1][=Branch1][N][C][=C][C][=C][Branch1][O][O][C][C][N][C][C][C][C][Ring1][Branch1][C][=C][Ring1][=C][N][=C][Ring2][Ring1][Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C],n-tert-butyl-3-[[5-methyl-2-[[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino]pyrimidin-4-yl]amino]benzenesulfonamide,2.11\nC[C@@H](N(c1cc(F)ccc1F)S(=O)(=O)c2ccc(Cl)cc2)c3ccc(F)cc3CCCC(=O)O,\"InChI=1S/C24H21ClF3NO4S/c1-15(21-11-7-18(26)13-16(21)3-2-4-24(30)31)29(23-14-19(27)8-12-22(23)28)34(32,33)20-9-5-17(25)6-10-20/h5-15H,2-4H2,1H3,(H,30,31)/t15-/m1/s1\",[C][C@@H1][Branch2][Ring2][C][N][Branch1][=N][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][C][C][=Branch1][C][=O][O],\"4-[2-[(1r)-1-[(4-chlorophenyl)sulfonyl-(2,5-difluorophenyl)amino]ethyl]-5-fluorophenyl]butanoic acid\",3.1\nCc1nc(CS(=O)(=O)c2ccccc2)cc(n1)N3CCOCC3,\"InChI=1S/C16H19N3O3S/c1-13-17-14(11-16(18-13)19-7-9-22-10-8-19)12-23(20,21)15-5-3-2-4-6-15/h2-6,11H,7-10,12H2,1H3\",[C][C][=N][C][Branch1][P][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Ring2][=N][Ring1][S][N][C][C][O][C][C][Ring1][=Branch1],2-methyl-4-morpholin-4-yl-6-(phenylsulfonylmethyl)pyrimidine,1.07\nCOc1ccc(cc1)[C@@H]2Sc3ccccc3N(CCN(C)C)C(=O)[C@@H]2OC(=O)C,\"InChI=1S/C22H26N2O4S/c1-15(25)28-20-21(16-9-11-17(27-4)12-10-16)29-19-8-6-5-7-18(19)24(22(20)26)14-13-23(2)3/h5-12,20-21H,13-14H2,1-4H3/t20-,21+/m1/s1\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][Branch2][C][C][N][Branch1][C][C][C][C][=Branch1][C][=O][C@@H1][Ring1][P][O][C][=Branch1][C][=O][C],\"[(2s,3s)-5-(2-dimethylaminoethyl)-2-(4-methoxyphenyl)-4-oxo-2,3-dihydro-1,5-benzothiazepin-3-yl] acetate\",1.99\nCc1ccc(cc1)S(=O)(=O)N2N=Cc3ccccc3B2O,\"InChI=1S/C14H13BN2O3S/c1-11-6-8-13(9-7-11)21(19,20)17-15(18)14-5-3-2-4-12(14)10-16-17/h2-10,18H,1H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][N][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][B][Ring1][#Branch2][O],\"1-hydroxy-2-(4-methylphenyl)sulfonyl-2,3,1-benzodiazaborinine\",0.05\nS=C(NC1CCCCC1)N2CCC(CC2)c3cnc[nH]3,\"InChI=1S/C15H24N4S/c20-15(18-13-4-2-1-3-5-13)19-8-6-12(7-9-19)14-10-16-11-17-14/h10-13H,1-9H2,(H,16,17)(H,18,20)\",[S][=C][Branch1][#Branch2][N][C][C][C][C][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][N][=C][NH1][Ring1][Branch1],n-cyclohexyl-4-(3h-imidazol-4-yl)piperidine-1-carbothioamide,2.3\nNc1cc(nc2ccccc12)c3ccccc3,\"InChI=1S/C15H12N2/c16-13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10H,(H2,16,17)\",[N][C][=C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-phenylquinolin-4-amine,2.2\nNC(=N)c1cc2c(cccc2s1)c3ccccc3,\"InChI=1S/C15H12N2S/c16-15(17)14-9-12-11(7-4-8-13(12)18-14)10-5-2-1-3-6-10/h1-9H,(H3,16,17)\",[N][C][=Branch1][C][=N][C][=C][C][=C][Branch1][#Branch2][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],4-phenyl-1-benzothiophene-2-carboximidamide,1.27\nClc1ccc(CN2C(=O)C(=O)c3ccccc23)cc1,\"InChI=1S/C15H10ClNO2/c16-11-7-5-10(6-8-11)9-17-13-4-2-1-3-12(13)14(18)15(17)19/h1-8H,9H2\",[Cl][C][=C][C][=C][Branch2][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][C],\"1-[(4-chlorophenyl)methyl]indole-2,3-dione\",3.1\nCC1CN(CCN1Cc2cc(Cl)ccc2OCC(=O)O)S(=O)(=O)c3ccccc3,\"InChI=1S/C20H23ClN2O5S/c1-15-12-23(29(26,27)18-5-3-2-4-6-18)10-9-22(15)13-16-11-17(21)7-8-19(16)28-14-20(24)25/h2-8,11,15H,9-10,12-14H2,1H3,(H,24,25)\",[C][C][C][N][Branch2][Ring1][=Branch2][C][C][N][Ring1][=Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-chloro-2-[(2-methyl-4-phenylsulfonylpiperazin-1-yl)methyl]phenoxy]acetic acid,0.69\nCC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccncc2)C(F)(F)F,\"InChI=1S/C15H13F3N2O4S/c1-14(22,15(16,17)18)13(21)20-10-2-4-11(5-3-10)25(23,24)12-6-8-19-9-7-12/h2-9,22H,1H3,(H,20,21)\",[C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"3,3,3-trifluoro-2-hydroxy-2-methyl-n-(4-pyridin-4-ylsulfonylphenyl)propanamide\",2.15\nCCN(CC)CCN1C(=O)[C@@](O)(c2ccccc2Cl)c3c1cc(cc3C(F)(F)F)C(=O)N,\"InChI=1S/C22H23ClF3N3O3/c1-3-28(4-2)9-10-29-17-12-13(19(27)30)11-15(22(24,25)26)18(17)21(32,20(29)31)14-7-5-6-8-16(14)23/h5-8,11-12,32H,3-4,9-10H2,1-2H3,(H2,27,30)/t21-/m1/s1\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C@@][Branch1][C][O][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][Ring1][=C][C][=C][Branch1][=N][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][N],(3s)-3-(2-chlorophenyl)-1-(2-diethylaminoethyl)-3-hydroxy-2-oxo-4-(trifluoromethyl)indole-6-carboxamide,2.4\nClc1ccc(cc1)C(=O)N[C@H]2CN3CCC2CC3,\"InChI=1S/C14H17ClN2O/c15-12-3-1-11(2-4-12)14(18)16-13-9-17-7-5-10(13)6-8-17/h1-4,10,13H,5-9H2,(H,16,18)/t13-/m0/s1\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@H1][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1],n-[(8r)-1-azabicyclo[2.2.2]octan-8-yl]-4-chlorobenzamide,0.6\nCC1=C(OCc2ccc(F)cc2)C(=O)C=CO1,\"InChI=1S/C13H11FO3/c1-9-13(12(15)6-7-16-9)17-8-10-2-4-11(14)5-3-10/h2-7H,8H2,1H3\",[C][C][=C][Branch1][=C][O][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][O][Ring1][S],3-[(4-fluorophenyl)methoxy]-2-methylpyran-4-one,1.91\nClc1ccc(cc1)C(=O)Cc2ccccn2,\"InChI=1S/C13H10ClNO/c14-11-6-4-10(5-7-11)13(16)9-12-3-1-2-8-15-12/h1-8H,9H2\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=N][Ring1][=Branch1],1-(4-chlorophenyl)-2-pyridin-2-ylethanone,2.96\nCOc1nc(Br)cnc1NS(=O)(=O)c2cccc3c(cccc23)N(C)C,\"InChI=1S/C17H17BrN4O3S/c1-22(2)13-8-4-7-12-11(13)6-5-9-14(12)26(23,24)21-16-17(25-3)20-15(18)10-19-16/h4-10H,1-3H3,(H,19,21)\",[C][O][C][=N][C][Branch1][C][Br][=C][N][=C][Ring1][#Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][Branch1][C][C][C],n-(5-bromo-3-methoxypyrazin-2-yl)-5-dimethylaminonaphthalene-1-sulfonamide,1.9\nNC(=O)c1sc2nccc(Nc3ccccc3)c2c1N,\"InChI=1S/C14H12N4OS/c15-11-10-9(18-8-4-2-1-3-5-8)6-7-17-14(10)20-12(11)13(16)19/h1-7H,15H2,(H2,16,19)(H,17,18)\",[N][C][=Branch1][C][=O][C][S][C][=N][C][=C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=Ring1][S][N],\"3-amino-4-(phenylamino)thieno[5,4-b]pyridine-2-carboxamide\",2.91\nCOc1ccccc1OCC(O)COC(=O)N,\"InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][N],[2-hydroxy-3-(2-methoxyphenoxy)propyl] carbamate,0.36\nOc1cc(O)c2C(=O)c3ccccc3Oc2c1,\"InChI=1S/C13H8O4/c14-7-5-9(15)12-11(6-7)17-10-4-2-1-3-8(10)13(12)16/h1-6,14-15H\",[O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][O][=C][Ring1][S],\"1,3-dihydroxyxanthen-9-one\",3.39\nCC1(C)CCC(CC1)NC(=O)[C@@H](N)CCC(=O)O,\"InChI=1S/C13H24N2O3/c1-13(2)7-5-9(6-8-13)15-12(18)10(14)3-4-11(16)17/h9-10H,3-8,14H2,1-2H3,(H,15,18)(H,16,17)/t10-/m0/s1\",[C][C][Branch1][C][C][C][C][C][Branch1][Branch1][C][C][Ring1][#Branch1][N][C][=Branch1][C][=O][C@@H1][Branch1][C][N][C][C][C][=Branch1][C][=O][O],\"(4s)-4-amino-5-[(4,4-dimethylcyclohexyl)amino]-5-oxopentanoic acid\",-0.27\nNS(=O)(=O)c1cc2c(NC(NS2(=O)=O)C3CC4CC3C=C4)cc1Cl,\"InChI=1S/C14H16ClN3O4S2/c15-10-5-11-13(6-12(10)23(16,19)20)24(21,22)18-14(17-11)9-4-7-1-2-8(9)3-7/h1-2,5-9,14,17-18H,3-4H2,(H2,16,19,20)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][Branch1][=Branch2][N][S][Ring1][=Branch1][=Branch1][C][=O][=O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring1][Branch1][C][=C][Ring2][Ring1][Ring1][Cl],\"3-(6-bicyclo[2.2.1]hept-2-enyl)-6-chloro-1,1-dioxo-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\",2.12\nOc1ccc(Br)c2ccccc12,\"InChI=1S/C10H7BrO/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6,12H\",[O][C][=C][C][=C][Branch1][C][Br][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1],4-bromonaphthalen-1-ol,4.3\nCCSc1ccc(cc1)c2cc(ccc2OCC(=O)O)C(F)(F)F,\"InChI=1S/C17H15F3O3S/c1-2-24-13-6-3-11(4-7-13)14-9-12(17(18,19)20)5-8-15(14)23-10-16(21)22/h3-9H,2,10H2,1H3,(H,21,22)\",[C][C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=N][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F],2-[2-(4-ethylsulfanylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid,1.54\nCOc1ccc(CN2C(=O)CCC2(C)C(=O)NC3CCCCC3)c(OC)c1,\"InChI=1S/C21H30N2O4/c1-21(20(25)22-16-7-5-4-6-8-16)12-11-19(24)23(21)14-15-9-10-17(26-2)13-18(15)27-3/h9-10,13,16H,4-8,11-12,14H2,1-3H3,(H,22,25)\",[C][O][C][=C][C][=C][Branch2][Ring1][N][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][=Branch2],\"n-cyclohexyl-1-[(2,4-dimethoxyphenyl)methyl]-2-methyl-5-oxopyrrolidine-2-carboxamide\",2.38\nO=C1C(=O)c2cc(ccc2c3ccccc13)c4ccsc4,InChI=1S/C18H10O2S/c19-17-15-4-2-1-3-13(15)14-6-5-11(9-16(14)18(17)20)12-7-8-21-10-12/h1-10H,[O][=C][C][=Branch1][C][=O][C][=C][C][=Branch1][S][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1][C][C][=C][S][C][=Ring1][Branch1],\"2-thiophen-3-ylphenanthrene-9,10-dione\",3.1\nCN(C)CC(O)COc1ccc(Nc2nccc(Nc3cc(Cl)ccc3Cl)n2)cc1,\"InChI=1S/C21H23Cl2N5O2/c1-28(2)12-16(29)13-30-17-6-4-15(5-7-17)25-21-24-10-9-20(27-21)26-19-11-14(22)3-8-18(19)23/h3-11,16,29H,12-13H2,1-2H3,(H2,24,25,26,27)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][Cl][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1],\"1-[4-[[4-[(2,5-dichlorophenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\",2.9\nCc1ccc(cc1)\\C(=C/CN2CCCC2)\\c3ccccn3,\"InChI=1S/C19H22N2/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21/h2-3,6-12H,4-5,13-15H2,1H3/b18-11+\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][\\C][=Branch1][#Branch2][=C][/C][N][C][C][C][C][Ring1][Branch1][\\C][=C][C][=C][C][=N][Ring1][=Branch1],2-[(e)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-enyl]pyridine,1.88\nCCCCC(CC)CNC(=O)c1cc(ccc1Cl)N2N=CC(=O)NC2=O,\"InChI=1S/C18H23ClN4O3/c1-3-5-6-12(4-2)10-20-17(25)14-9-13(7-8-15(14)19)23-18(26)22-16(24)11-21-23/h7-9,11-12H,3-6,10H2,1-2H3,(H,20,25)(H,22,24,26)\",[C][C][C][C][C][Branch1][Ring1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O],\"2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)-n-(2-ethylhexyl)benzamide\",2.41\nCc1c(Sc2ccc(Cl)cc2)c3c(cccc3n1CC(=O)O)c4cnccn4,\"InChI=1S/C21H16ClN3O2S/c1-13-21(28-15-7-5-14(22)6-8-15)20-16(17-11-23-9-10-24-17)3-2-4-18(20)25(13)12-19(26)27/h2-11H,12H2,1H3,(H,26,27)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][S][C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][=C][N][=C][C][=N][Ring1][=Branch1],2-[3-(4-chlorophenyl)sulfanyl-2-methyl-4-pyrazin-2-ylindol-1-yl]acetic acid,0.03\nC(Oc1ccccc1)C2CNCCO2,\"InChI=1S/C11H15NO2/c1-2-4-10(5-3-1)14-9-11-8-12-6-7-13-11/h1-5,11-12H,6-9H2\",[C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][N][C][C][O][Ring1][=Branch1],2-(phenoxymethyl)morpholine,0.2\nCCN(CC)CCNC(=O)c1c(C)[nH]c(\\C=C\\2/C(=O)Nc3ccc(F)cc23)c1C,\"InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12-\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][NH1][C][Branch2][Ring1][Branch1][\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][\\-Ring1][O][Ring1][#Branch1][=C][Ring2][Ring1][C][C],\"n-(2-diethylaminoethyl)-5-[(z)-(5-fluoro-2-oxo-1h-indol-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide\",2.26\nClc1ccc(OC2CCN(CC2)C3CCN(CC3)C(=O)NS(=O)(=O)c4ccccc4)cc1Cl,\"InChI=1S/C23H27Cl2N3O4S/c24-21-7-6-19(16-22(21)25)32-18-10-14-27(15-11-18)17-8-12-28(13-9-17)23(29)26-33(30,31)20-4-2-1-3-5-20/h1-7,16-18H,8-15H2,(H,26,29)\",[Cl][C][=C][C][=C][Branch2][Ring2][#Branch2][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][#C][Cl],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-phenylsulfonylpiperidine-1-carboxamide\",1.5\nFc1ccc(cc1)[C@@H]2CCNC[C@H]2COc3ccc4OCOc4c3,\"InChI=1S/C19H20FNO3/c20-15-3-1-13(2-4-15)17-7-8-21-10-14(17)11-22-16-5-6-18-19(9-16)24-12-23-18/h1-6,9,14,17,21H,7-8,10-12H2/t14-,17-/m0/s1\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][C][C][N][C][C@H1][Ring1][=Branch1][C][O][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2],\"(3s,4r)-3-(1,3-benzodioxol-5-yloxymethyl)-4-(4-fluorophenyl)piperidine\",1.78\nCN1CCN(CCCOc2ccc(cc2)c3onc(c3)c4ccc(F)cc4)CC1,\"InChI=1S/C23H26FN3O2/c1-26-12-14-27(15-13-26)11-2-16-28-21-9-5-19(6-10-21)23-17-22(25-29-23)18-3-7-20(24)8-4-18/h3-10,17H,2,11-16H2,1H3\",[C][N][C][C][N][Branch2][Ring2][Ring1][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][O][N][=C][Branch1][Ring2][C][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][N],\"1-[3-[4-[3-(4-fluorophenyl)-1,2-oxazol-5-yl]phenoxy]propyl]-4-methylpiperazine\",3.81\nCNc1ccc(cc1)c2nc3ccc(O)cc3s2,\"InChI=1S/C14H12N2OS/c1-15-10-4-2-9(3-5-10)14-16-12-7-6-11(17)8-13(12)18-14/h2-8,15,17H,1H3\",[C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][S][Ring1][#Branch2],\"2-(4-methylaminophenyl)-1,3-benzothiazol-6-ol\",3.5\nCN1CCN(CC1)C(=O)c2cc3cc(F)ccc3[nH]2,\"InChI=1S/C14H16FN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],(5-fluoro-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone,1.97\nO=C1C2CCC(N2)C(=O)N1Cc3ccccc3,\"InChI=1S/C13H14N2O2/c16-12-10-6-7-11(14-10)13(17)15(12)8-9-4-2-1-3-5-9/h1-5,10-11,14H,6-8H2\",[O][=C][C][C][C][C][Branch1][Ring2][N][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][=Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-(phenylmethyl)-3,8-diazabicyclo[3.2.1]octane-2,4-dione\",2.21\nCN1N=Nc2c(ncn2C1=O)C(=O)N,\"InChI=1S/C6H6N6O2/c1-11-6(14)12-2-8-3(4(7)13)5(12)9-10-11/h2H,1H3,(H2,7,13)\",[C][N][N][=N][C][=C][Branch1][#Branch2][N][=C][N][Ring1][Branch1][C][Ring1][=Branch2][=O][C][=Branch1][C][=O][N],\"3-methyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide\",-1.08\nFc1cc2[nH]cnc2cc1Cl,\"InChI=1S/C7H4ClFN2/c8-4-1-6-7(2-5(4)9)11-3-10-6/h1-3H,(H,10,11)\",[F][C][=C][C][NH1][C][=N][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][Cl],5-chloro-6-fluoro-1h-benzimidazole,2.35\nCCN(CC)C(=O)Cc1csc(NS(=O)(=O)c2cccc(Cl)c2C)n1,\"InChI=1S/C16H20ClN3O3S2/c1-4-20(5-2)15(21)9-12-10-24-16(18-12)19-25(22,23)14-8-6-7-13(17)11(14)3/h6-8,10H,4-5,9H2,1-3H3,(H,18,19)\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][C][=C][S][C][Branch2][Ring1][Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][Ring1][P],\"2-[2-[(3-chloro-2-methylphenyl)sulfonylamino]-1,3-thiazol-4-yl]-n,n-diethylacetamide\",1.67\nCCCN(CCO)CCCOc1ccc2c(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)ncnc2c1,\"InChI=1S/C27H31F2N7O3/c1-2-9-36(11-12-37)10-4-13-39-19-7-8-20-23(16-19)30-17-31-27(20)33-24-14-18(34-35-24)15-25(38)32-22-6-3-5-21(28)26(22)29/h3,5-8,14,16-17,37H,2,4,9-13,15H2,1H3,(H,32,38)(H2,30,31,33,34,35)\",[C][C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=C][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=N][C][=N][C][Ring2][Ring1][Branch2][=C][Ring2][Ring1][N],\"n-(2,3-difluorophenyl)-2-[5-[[7-[3-(2-hydroxyethyl-propylamino)propoxy]quinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\",2.19\nCc1oc(cc1C(=O)Nc2cccc(c2)C(=O)O)c3ccccc3,\"InChI=1S/C19H15NO4/c1-12-16(11-17(24-12)13-6-3-2-4-7-13)18(21)20-15-9-5-8-14(10-15)19(22)23/h2-11H,1H3,(H,20,21)(H,22,23)\",[C][C][O][C][=Branch2][Ring1][=Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1],3-[(2-methyl-5-phenylfuran-3-carbonyl)amino]benzoic acid,1.63\nCCN(CC)S(=O)(=O)c1ccc(NC(=O)C(C)(O)C(F)(F)F)cc1,\"InChI=1S/C14H19F3N2O4S/c1-4-19(5-2)24(22,23)11-8-6-10(7-9-11)18-12(20)13(3,21)14(15,16)17/h6-9,21H,4-5H2,1-3H3,(H,18,20)\",[C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][S],\"n-[4-(diethylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",2.63\nCOc1ccc2NC(=O)C(NC(=O)c3ccccc3OC)N=C(c4ccccc4)c2c1,\"InChI=1S/C24H21N3O4/c1-30-16-12-13-19-18(14-16)21(15-8-4-3-5-9-15)26-22(24(29)25-19)27-23(28)17-10-6-7-11-20(17)31-2/h3-14,22H,1-2H3,(H,25,29)(H,27,28)\",[C][O][C][=C][C][=C][N][C][=Branch1][C][=O][C][Branch1][S][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][=C][Ring2][Ring1][=N],\"2-methoxy-n-(7-methoxy-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl)benzamide\",3.8\nCC(CO)(CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)sc13,\"InChI=1S/C16H17F2N5O2S2/c1-16(6-24,7-25)23-13-11-12(20-14(19)27-11)21-15(22-13)26-5-8-3-2-4-9(17)10(8)18/h2-4,24-25H,5-7H2,1H3,(H3,19,20,21,22,23)\",[C][C][Branch1][Ring1][C][O][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1],\"2-[[2-amino-5-[(2,3-difluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]-2-methylpropane-1,3-diol\",2.87\nCOC(=O)COc1ccc(OCCNCC(O)COc2ccccc2)cc1,\"InChI=1S/C20H25NO6/c1-24-20(23)15-27-19-9-7-18(8-10-19)25-12-11-21-13-16(22)14-26-17-5-3-2-4-6-17/h2-10,16,21-22H,11-15H2,1H3\",[C][O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch2][Ring1][Ring2][O][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1],methyl 2-[4-[2-[[2-hydroxy-3-(phenoxy)propyl]amino]ethoxy]phenoxy]acetate,1.54\nCOc1ccnc(CSc2nc3ccccc3[nH]2)c1,\"InChI=1S/C14H13N3OS/c1-18-11-6-7-15-10(8-11)9-19-14-16-12-4-2-3-5-13(12)17-14/h2-8H,9H2,1H3,(H,16,17)\",[C][O][C][=C][C][=N][C][Branch1][S][C][S][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][=C][Ring1][P],2-[(4-methoxypyridin-2-yl)methylsulfanyl]-1h-benzimidazole,2.89\nFc1ncccc1OC[C@@H]2CCN2,\"InChI=1S/C9H11FN2O/c10-9-8(2-1-4-12-9)13-6-7-3-5-11-7/h1-2,4,7,11H,3,5-6H2/t7-/m0/s1\",[F][C][=N][C][=C][C][=C][Ring1][=Branch1][O][C][C@@H1][C][C][N][Ring1][Ring2],3-[[(2s)-azetidin-2-yl]methoxy]-2-fluoropyridine,-1.2\nCc1ccnc(NCc2ccc(Cl)cc2)c1,\"InChI=1S/C13H13ClN2/c1-10-6-7-15-13(8-10)16-9-11-2-4-12(14)5-3-11/h2-8H,9H2,1H3,(H,15,16)\",[C][C][=C][C][=N][C][Branch1][=C][N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Ring1][#C],n-[(4-chlorophenyl)methyl]-4-methylpyridin-2-amine,3.6\nCCN(CCO)CCCOc1cc2ncnc(Nc3cc(CC(=O)Nc4cccc(F)c4)[nH]n3)c2cc1OC,\"InChI=1S/C27H32FN7O4/c1-3-35(9-10-36)8-5-11-39-24-16-22-21(15-23(24)38-2)27(30-17-29-22)32-25-13-20(33-34-25)14-26(37)31-19-7-4-6-18(28)12-19/h4,6-7,12-13,15-17,36H,3,5,8-11,14H2,1-2H3,(H,31,37)(H2,29,30,32,33,34)\",[C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=N][N][C][C][=C][Branch2][Ring1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][NH1][N][=Ring1][S][=C][Ring2][Ring1][#Branch1][C][=C][Ring2][Ring1][O][O][C],2-[5-[[7-[3-(ethyl-(2-hydroxyethyl)amino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]-n-(3-fluorophenyl)acetamide,2.12\nNc1nc(N)c(c(COCc2ccccc2)n1)c3ccc(NC(=O)C4CC4)cc3,\"InChI=1S/C22H23N5O2/c23-20-19(15-8-10-17(11-9-15)25-21(28)16-6-7-16)18(26-22(24)27-20)13-29-12-14-4-2-1-3-5-14/h1-5,8-11,16H,6-7,12-13H2,(H,25,28)(H4,23,24,26,27)\",[N][C][=N][C][Branch1][C][N][=C][Branch2][Ring1][C][C][Branch1][N][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][S][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][C][C][C][Ring1][Ring1][C][=C][Ring1][N],\"n-[4-[2,4-diamino-6-(phenylmethoxymethyl)pyrimidin-5-yl]phenyl]cyclopropanecarboxamide\",2.46\nClc1ccc(OC2CCN(CC2)C3CCN(CC3)C(=O)NS(=O)(=O)Cc4ccccc4)cc1Cl,\"InChI=1S/C24H29Cl2N3O4S/c25-22-7-6-21(16-23(22)26)33-20-10-14-28(15-11-20)19-8-12-29(13-9-19)24(30)27-34(31,32)17-18-4-2-1-3-5-18/h1-7,16,19-20H,8-15,17H2,(H,27,30)\",[Cl][C][=C][C][=C][Branch2][Ring2][O][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][S][Cl],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(phenylmethylsulfonyl)piperidine-1-carboxamide\",2.13\nCSc1nc(C(=O)N)c(N)s1,\"InChI=1S/C5H7N3OS2/c1-10-5-8-2(3(6)9)4(7)11-5/h7H2,1H3,(H2,6,9)\",[C][S][C][=N][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][C][N][S][Ring1][=Branch2],\"5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide\",1.21\nCOc1ccccc1CN(C(=O)C)c2cnccc2Oc3ccccc3,\"InChI=1S/C21H20N2O3/c1-16(24)23(15-17-8-6-7-11-20(17)25-2)19-14-22-13-12-21(19)26-18-9-4-3-5-10-18/h3-14H,15H2,1-2H3\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=C][N][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1],n-[(2-methoxyphenyl)methyl]-n-[4-(phenoxy)pyridin-3-yl]acetamide,3\nc1ccc2ncccc2c1,InChI=1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H,[C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],quinoline,2.09\nC[C@H](NC1=NC(=O)[C@@](C)(S1)C(F)(F)F)c2ccccc2F,\"InChI=1S/C13H12F4N2OS/c1-7(8-5-3-4-6-9(8)14)18-11-19-10(20)12(2,21-11)13(15,16)17/h3-7H,1-2H3,(H,18,19,20)/t7-,12+/m0/s1\",[C][C@H1][Branch2][Ring1][=Branch2][N][C][=N][C][=Branch1][C][=O][C@@][Branch1][C][C][Branch1][Ring2][S][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F],\"(5r)-2-[[(1s)-1-(2-fluorophenyl)ethyl]amino]-5-methyl-5-(trifluoromethyl)-1,3-thiazol-4-one\",3.1\nC[C@@H](N)COc1c(C)cccc1C,\"InChI=1S/C11H17NO/c1-8-5-4-6-9(2)11(8)13-7-10(3)12/h4-6,10H,7,12H2,1-3H3/t10-/m1/s1\",[C][C@@H1][Branch1][C][N][C][O][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C],\"(2r)-1-(2,6-dimethylphenoxy)propan-2-amine\",0.6\nCC1N=C(N)N=C(N)N1c2ccc(Cl)cc2,\"InChI=1S/C10H12ClN5/c1-6-14-9(12)15-10(13)16(6)8-4-2-7(11)3-5-8/h2-6H,1H3,(H4,12,13,14,15)\",[C][C][N][=C][Branch1][C][N][N][=C][Branch1][C][N][N][Ring1][Branch2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"1-(4-chlorophenyl)-6-methyl-6h-1,3,5-triazine-2,4-diamine\",-0.8\nCc1ccccc1N2C(=Nc3cccc(C)c3C2=O)Cn4cnc5c(N)ncnc45,\"InChI=1S/C22H19N7O/c1-13-6-3-4-9-16(13)29-17(27-15-8-5-7-14(2)18(15)22(29)30)10-28-12-26-19-20(23)24-11-25-21(19)28/h3-9,11-12H,10H2,1-2H3,(H2,23,24,25)\",[C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][P][=N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C][Ring1][O][=O][C][N][C][=N][C][=C][Branch1][C][N][N][=C][N][=C][Ring1][#Branch2][Ring1][#Branch1],2-[(6-aminopurin-9-yl)methyl]-5-methyl-3-(2-methylphenyl)quinazolin-4-one,2.6\nCOc1ccc2nc3ccccc3c(N)c2c1,\"InChI=1S/C14H12N2O/c1-17-9-6-7-13-11(8-9)14(15)10-4-2-3-5-12(10)16-13/h2-8H,1H3,(H2,15,16)\",[C][O][C][=C][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][N][C][Ring1][O][=C][Ring1][#C],2-methoxyacridin-9-amine,1\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(cccc34)C(F)(F)F,\"InChI=1S/C22H17F3N2O2/c1-12-6-7-18-16(10-12)20(13(2)27(18)11-19(28)29)14-8-9-26-21-15(14)4-3-5-17(21)22(23,24)25/h3-10H,11H2,1-2H3,(H,28,29)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"2-[2,5-dimethyl-3-[8-(trifluoromethyl)quinolin-4-yl]indol-1-yl]acetic acid\",1.27\nCc1oncc1C(=O)Nc2ccc(cc2)C(F)(F)F,\"InChI=1S/C12H9F3N2O2/c1-7-10(6-16-19-7)11(18)17-9-4-2-8(3-5-9)12(13,14)15/h2-6H,1H3,(H,17,18)\",[C][C][O][N][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"5-methyl-n-[4-(trifluoromethyl)phenyl]-1,2-oxazole-4-carboxamide\",3.9\nCOc1ccc(cc1OC)C(=O)Nc2cc(NC(=O)c3cccc(c3)N(C)C)ccc2C,\"InChI=1S/C25H27N3O4/c1-16-9-11-19(26-24(29)17-7-6-8-20(13-17)28(2)3)15-21(16)27-25(30)18-10-12-22(31-4)23(14-18)32-5/h6-15H,1-5H3,(H,26,29)(H,27,30)\",[C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][=C][C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][C][C],\"n-[5-[(3-dimethylaminobenzoyl)amino]-2-methylphenyl]-3,4-dimethoxybenzamide\",3.12\nNc1cc(ncn1)c2ccccc2,\"InChI=1S/C10H9N3/c11-10-6-9(12-7-13-10)8-4-2-1-3-5-8/h1-7H,(H2,11,12,13)\",[N][C][=C][C][=Branch1][=Branch1][=N][C][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],6-phenylpyrimidin-4-amine,1.91\nCc1onc(NS(=O)(=O)c2ccc(N)cc2)c1,\"InChI=1S/C10H11N3O3S/c1-7-6-10(12-16-7)13-17(14,15)9-4-2-8(11)3-5-9/h2-6H,11H2,1H3,(H,12,13)\",[C][C][O][N][=C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][C][=Ring1][S],\"4-amino-n-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide\",-0.56\nClc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4cc5ccccc5s4)C3=O,\"InChI=1S/C20H12ClN3O3S/c21-11-5-6-13-14(8-11)22-17-16(18(13)25)20(27)24(23-19(17)26)9-12-7-10-3-1-2-4-15(10)28-12/h1-8H,9H2,(H,22,25)(H,23,26)\",[Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][#C][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][Ring2][Ring1][Ring2][=O],\"2-(1-benzothiophen-2-ylmethyl)-7-chloro-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",2\nCC(C)c1cc(C(=O)N2Cc3ccc(CN4CCN(C)CC4)cc3C2)c(O)cc1O,\"InChI=1S/C24H31N3O3/c1-16(2)20-11-21(23(29)12-22(20)28)24(30)27-14-18-5-4-17(10-19(18)15-27)13-26-8-6-25(3)7-9-26/h4-5,10-12,16,28-29H,6-9,13-15H2,1-3H3\",[C][C][Branch1][C][C][C][=C][C][Branch2][Ring1][S][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][=N][C][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=C][Ring1][=C][C][Ring1][P][=C][Branch1][C][O][C][=C][Ring2][Ring1][#Branch2][O],\"(2,4-dihydroxy-5-propan-2-ylphenyl)-[5-[(4-methylpiperazin-1-yl)methyl]-1,3-dihydroisoindol-2-yl]methanone\",2.5\nCOC1(CCOCC1)c2cc(F)cc(OCc3ccc4N(C)C(=O)C=Cc4c3)c2,\"InChI=1S/C23H24FNO4/c1-25-21-5-3-16(11-17(21)4-6-22(25)26)15-29-20-13-18(12-19(24)14-20)23(27-2)7-9-28-10-8-23/h3-6,11-14H,7-10,15H2,1-2H3\",[C][O][C][Branch1][Branch2][C][C][O][C][C][Ring1][=Branch1][C][=C][C][Branch1][C][F][=C][C][Branch2][Ring1][#Branch1][O][C][C][=C][C][=C][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][Ring1][Branch2][=C][Ring1][N][=C][Ring2][Ring1][Branch1],6-[[3-fluoro-5-(4-methoxyoxan-4-yl)phenoxy]methyl]-1-methylquinolin-2-one,3.52\nC[C@H](Nc1ncc(F)c(Nc2cc(C)[nH]n2)n1)c3ncc(F)cn3,\"InChI=1S/C14H14F2N8/c1-7-3-11(24-23-7)21-13-10(16)6-19-14(22-13)20-8(2)12-17-4-9(15)5-18-12/h3-6,8H,1-2H3,(H3,19,20,21,22,23,24)/t8-/m0/s1\",[C][C@H1][Branch2][Ring1][#Branch2][N][C][=N][C][=C][Branch1][C][F][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=N][Ring1][=C][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1],\"5-fluoro-n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-n'-(5-methyl-1h-pyrazol-3-yl)pyrimidine-2,4-diamine\",1.79\nC(Nc1ncnc2ccccc12)c3ccccc3,\"InChI=1S/C15H13N3/c1-2-6-12(7-3-1)10-16-15-13-8-4-5-9-14(13)17-11-18-15/h1-9,11H,10H2,(H,16,17,18)\",[C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-(phenylmethyl)quinazolin-4-amine,3.21\nCC(N1C(=O)c2ccccc2C1=O)C(=O)N3CCc4ccccc4C3,\"InChI=1S/C20H18N2O3/c1-13(22-19(24)16-8-4-5-9-17(16)20(22)25)18(23)21-11-10-14-6-2-3-7-15(14)12-21/h2-9,13H,10-12H2,1H3\",[C][C][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2],\"2-[1-(3,4-dihydro-1h-isoquinolin-2-yl)-1-oxopropan-2-yl]isoindole-1,3-dione\",2.47\nNc1ccc(cc1)C2(CCCCC2)c3ccc(N)cc3,\"InChI=1S/C18H22N2/c19-16-8-4-14(5-9-16)18(12-2-1-3-13-18)15-6-10-17(20)11-7-15/h4-11H,1-3,12-13,19-20H2\",[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],4-[1-(4-aminophenyl)cyclohexyl]aniline,3.2\nCS(=O)(=O)c1ccc(cc1)[C@@H](CC2CCCC2)C(=O)Nc3nccs3,\"InChI=1S/C18H22N2O3S2/c1-25(22,23)15-8-6-14(7-9-15)16(12-13-4-2-3-5-13)17(21)20-18-19-10-11-24-18/h6-11,13,16H,2-5,12H2,1H3,(H,19,20,21)/t16-/m1/s1\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"(2r)-3-cyclopentyl-2-(4-methylsulfonylphenyl)-n-(1,3-thiazol-2-yl)propanamide\",3.86\nCCN(CC)CCNC(=O)c1c(C)[nH]c(\\C=C\\2/C(=O)Nc3ccc(Cl)cc23)c1C,\"InChI=1S/C22H27ClN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12-\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][NH1][C][Branch2][Ring1][Branch1][\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][\\-Ring1][O][Ring1][#Branch1][=C][Ring2][Ring1][C][C],\"5-[(z)-(5-chloro-2-oxo-1h-indol-3-ylidene)methyl]-n-(2-diethylaminoethyl)-2,4-dimethyl-1h-pyrrole-3-carboxamide\",2.75\nCC(C)(C)OC(=O)N1CCC(CC1)OCc2onc(n2)c3ccncc3,\"InChI=1S/C18H24N4O4/c1-18(2,3)25-17(23)22-10-6-14(7-11-22)24-12-15-20-16(21-26-15)13-4-8-19-9-5-13/h4-5,8-9,14H,6-7,10-12H2,1-3H3\",[C][C][Branch1][C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][C][O][N][=C][Branch1][Ring2][N][=Ring1][Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1],\"tert-butyl 4-[(3-pyridin-4-yl-1,2,4-oxadiazol-5-yl)methoxy]piperidine-1-carboxylate\",3\nC[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)C)C(F)(F)F,\"InChI=1S/C11H11ClF3NO4S/c1-10(18,11(13,14)15)9(17)16-8-4-3-6(5-7(8)12)21(2,19)20/h3-5,18H,1-2H3,(H,16,17)/t10-/m1/s1\",[C][C@@][Branch1][C][O][Branch2][Ring1][=Branch2][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Branch1][C][F][Branch1][C][F][F],\"(2r)-n-(2-chloro-4-methylsulfonylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",2.08\nClc1ccc2nsnc2c1NC3=NCCN3,\"InChI=1S/C9H8ClN5S/c10-5-1-2-6-8(15-16-14-6)7(5)13-9-11-3-4-12-9/h1-2H,3-4H2,(H2,11,12,13)\",[Cl][C][C][=C][C][=N][S][N][=C][Ring1][Branch1][C][=Ring1][=Branch2][N][C][=N][C][C][N][Ring1][Branch1],\"6-chloro-n-(4,5-dihydro-1h-imidazol-2-yl)-2,1,3-benzothiadiazol-7-amine\",0.71\nCCS(=O)(=O)Nc1cccc2c1c(Oc3ccc(Cl)cc3)c(C)n2CC(=O)O,\"InChI=1S/C19H19ClN2O5S/c1-3-28(25,26)21-15-5-4-6-16-18(15)19(12(2)22(16)11-17(23)24)27-14-9-7-13(20)8-10-14/h4-10,21H,3,11H2,1-2H3,(H,23,24)\",[C][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O],2-[3-(4-chlorophenoxy)-4-(ethylsulfonylamino)-2-methylindol-1-yl]acetic acid,-0.29\nCN1CCN(Cc2ccc(cc2)C(=O)Nc3ccc(C)c(Nc4nccc(n4)c5cccnc5)c3)CC1,\"InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34)\",[C][N][C][C][N][Branch2][Branch1][Ring1][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch2][Ring1][Ring2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][=C][Ring2][Ring1][Ring2][C][C][Ring2][Ring2][Ring2],4-[(4-methylpiperazin-1-yl)methyl]-n-[4-methyl-3-[(4-pyridin-3-ylpyrimidin-2-yl)amino]phenyl]benzamide,2.5\nCCCCNc1nc(SCCC)nc2c1nnn2[C@@H]3C[C@H](CO)[C@@H](O)[C@H]3O,\"InChI=1S/C17H28N6O3S/c1-3-5-6-18-15-12-16(20-17(19-15)27-7-4-2)23(22-21-12)11-8-10(9-24)13(25)14(11)26/h10-11,13-14,24-26H,3-9H2,1-2H3,(H,18,19,20)/t10-,11-,13-,14+/m1/s1\",[C][C][C][C][N][C][=N][C][Branch1][Branch1][S][C][C][C][=N][C][=C][Ring1][#Branch2][N][=N][N][Ring1][Branch1][C@@H1][C][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O],\"(1r,2s,3r,5r)-3-(7-butylamino-5-propylsulfanyltriazolo[5,4-d]pyrimidin-3-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol\",3.07\nOC(=O)c1ccccc1Nc2cccc(c2)C(F)(F)F,\"InChI=1S/C14H10F3NO2/c15-14(16,17)9-4-3-5-10(8-9)18-12-7-2-1-6-11(12)13(19)20/h1-8,18H,(H,19,20)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],2-[[3-(trifluoromethyl)phenyl]amino]benzoic acid,2.01\nCC1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1S(=O)(=O)c3ccccc3,\"InChI=1S/C20H23ClN2O5S/c1-15-12-22(9-10-23(15)29(26,27)18-5-3-2-4-6-18)13-16-11-17(21)7-8-19(16)28-14-20(24)25/h2-8,11,15H,9-10,12-14H2,1H3,(H,24,25)\",[C][C][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-chloro-2-[(3-methyl-4-phenylsulfonylpiperazin-1-yl)methyl]phenoxy]acetic acid,0.31\nCc1ccccc1S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C24H29Cl2N3O4S/c1-17-4-2-3-5-23(17)34(31,32)27-24(30)29-12-8-18(9-13-29)28-14-10-19(11-15-28)33-20-6-7-21(25)22(26)16-20/h2-7,16,18-19H,8-15H2,1H3,(H,27,30)\",[C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(2-methylphenyl)sulfonylpiperidine-1-carboxamide\",1.71\nCCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N2[C@H]3CCC[C@H]3C[C@H]2C(=O)O,\"InChI=1S/C23H32N2O5/c1-3-30-23(29)18(13-12-16-8-5-4-6-9-16)24-15(2)21(26)25-19-11-7-10-17(19)14-20(25)22(27)28/h4-6,8-9,15,17-20,24H,3,7,10-14H2,1-2H3,(H,27,28)/t15-,17-,18-,19-,20-/m0/s1\",[C][C][O][C][=Branch1][C][=O][C@H1][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][C@H1][Ring1][Branch1][C][C@H1][Ring1][Branch2][C][=Branch1][C][=O][O],\"(2s,3as,6as)-1-[(2s)-2-[[(2s)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]-3,3a,4,5,6,6a-hexahydro-2h-cyclopenta[d]pyrrole-2-carboxylic acid\",-0.41\nOC(=O)c1cn(Cc2ccccc2)c3ccccc13,\"InChI=1S/C16H13NO2/c18-16(19)14-11-17(10-12-6-2-1-3-7-12)15-9-5-4-8-13(14)15/h1-9,11H,10H2,(H,18,19)\",[O][C][=Branch1][C][=O][C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1],1-(phenylmethyl)indole-3-carboxylic acid,1.19\nCCN1CCN(Cc2cnc(c(Cl)c2)c3ccc(cc3)C(=O)Nc4ccccc4N)CC1,\"InChI=1S/C25H28ClN5O/c1-2-30-11-13-31(14-12-30)17-18-15-21(26)24(28-16-18)19-7-9-20(10-8-19)25(32)29-23-6-4-3-5-22(23)27/h3-10,15-16H,2,11-14,17,27H2,1H3,(H,29,32)\",[C][C][N][C][C][N][Branch2][Ring2][#Branch1][C][C][=C][N][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][Ring2][Ring1][=C],n-(2-aminophenyl)-4-[3-chloro-5-[(4-ethylpiperazin-1-yl)methyl]pyridin-2-yl]benzamide,1.81\nCNC(=O)Nc1cc(sc1C(=O)N)c2ccccc2,\"InChI=1S/C13H13N3O2S/c1-15-13(18)16-9-7-10(19-11(9)12(14)17)8-5-3-2-4-6-8/h2-7H,1H3,(H2,14,17)(H2,15,16,18)\",[C][N][C][=Branch1][C][=O][N][C][C][=C][Branch1][#Branch2][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],3-(methylcarbamoylamino)-5-phenylthiophene-2-carboxamide,2.71\nCc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3ccc(C)cc3,\"InChI=1S/C21H23NO2/c1-15-3-7-17(8-4-15)20(23)18-11-13-22(14-12-18)21(24)19-9-5-16(2)6-10-19/h3-10,18H,11-14H2,1-2H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],[1-(4-methylbenzoyl)piperidin-4-yl]-(4-methylphenyl)methanone,3.43\nCc1ncc(c2ccnc(Nc3ccc(cc3)S(=O)(=O)N)n2)n1C,\"InChI=1S/C15H16N6O2S/c1-10-18-9-14(21(10)2)13-7-8-17-15(20-13)19-11-3-5-12(6-4-11)24(16,22)23/h3-9H,1-2H3,(H2,16,22,23)(H,17,19,20)\",[C][C][=N][C][=C][Branch2][Ring1][#C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][Ring1][P][N][Ring2][Ring1][=Branch1][C],\"4-[[4-(2,3-dimethylimidazol-4-yl)pyrimidin-2-yl]amino]benzenesulfonamide\",1.6\nNC1=NC(Nc2cccc(F)c12)c3cccs3,\"InChI=1S/C12H10FN3S/c13-7-3-1-4-8-10(7)11(14)16-12(15-8)9-5-2-6-17-9/h1-6,12,15H,(H2,14,16)\",[N][C][=N][C][Branch1][#C][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][O][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1],\"5-fluoro-2-thiophen-2-yl-1,2-dihydroquinazolin-4-amine\",0.91\nCN1C(=O)CN=C(c2ccccc2)c3cc(Cl)ccc13,\"InChI=1S/C16H13ClN2O/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\",[C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#Branch1],\"7-chloro-1-methyl-5-phenyl-3h-1,4-benzodiazepin-2-one\",2.69\nCC(C)(N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc3c[nH]c4ccccc34)NC=O,\"InChI=1S/C26H30N6O3/c1-26(2,27)25(35)31-22(11-16-13-28-20-9-5-3-7-18(16)20)24(34)32-23(30-15-33)12-17-14-29-21-10-6-4-8-19(17)21/h3-10,13-15,22-23,28-29H,11-12,27H2,1-2H3,(H,30,33)(H,31,35)(H,32,34)/t22-,23-/m1/s1\",[C][C][Branch1][C][C][Branch1][C][N][C][=Branch1][C][=O][N][C@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N][C@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=O],2-amino-n-[(2r)-1-[[(1r)-1-formamido-2-(1h-indol-3-yl)ethyl]amino]-3-(1h-indol-3-yl)-1-oxopropan-2-yl]-2-methylpropanamide,1\nCCC1(NC(=O)N(C)C1=O)c2ccccc2,\"InChI=1S/C12H14N2O2/c1-3-12(9-7-5-4-6-8-9)10(15)14(2)11(16)13-12/h4-8H,3H2,1-2H3,(H,13,16)\",[C][C][C][Branch1][=C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-ethyl-3-methyl-5-phenylimidazolidine-2,4-dione\",1.59\nCc1c(CCC(=O)O)c[nH]c1\\C=C\\2/C(=O)Nc3ccccc23,\"InChI=1S/C17H16N2O3/c1-10-11(6-7-16(20)21)9-18-15(10)8-13-12-4-2-3-5-14(12)19-17(13)22/h2-5,8-9,18H,6-7H2,1H3,(H,19,22)(H,20,21)/b13-8-\",[C][C][C][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][=C][NH1][C][=Ring1][#Branch2][\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][\\-Ring1][#Branch2][Ring1][=Branch1],3-[4-methyl-5-[(z)-(2-oxo-1h-indol-3-ylidene)methyl]-1h-pyrrol-3-yl]propanoic acid,1.05\nCOc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC4CCN(C)CC4,\"InChI=1S/C21H22ClFN4O2/c1-27-8-6-13(7-9-27)29-19-10-14-17(11-18(19)28-2)24-12-25-21(14)26-16-5-3-4-15(22)20(16)23/h3-5,10-13H,6-9H2,1-2H3,(H,24,25,26)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],n-(3-chloro-2-fluorophenyl)-7-methoxy-6-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine,2.72\nCNCC[C@H](Oc1cccc2ccccc12)c3cccs3,\"InChI=1S/C18H19NOS/c1-19-12-11-17(18-10-5-13-21-18)20-16-9-4-7-14-6-2-3-8-15(14)16/h2-10,13,17,19H,11-12H2,1H3/t17-/m0/s1\",[C][N][C][C][C@H1][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][S][Ring1][Branch1],(3s)-n-methyl-3-naphthalen-1-yloxy-3-thiophen-2-ylpropan-1-amine,2.09\nCC(N1Cc2ccccc2C1=O)c3ccccc3,\"InChI=1S/C16H15NO/c1-12(13-7-3-2-4-8-13)17-11-14-9-5-6-10-15(14)16(17)18/h2-10,12H,11H2,1H3\",[C][C][Branch1][#C][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(1-phenylethyl)-3h-isoindol-1-one,3\nOC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4sc(Cl)c(Cl)c4[nH]3,\"InChI=1S/C18H13Cl2N3O4S/c19-14-15-12(28-16(14)20)6-9(21-15)17(26)22-10-5-8-3-1-2-4-11(8)23(18(10)27)7-13(24)25/h1-4,6,10,21H,5,7H2,(H,22,26)(H,24,25)\",[O][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][S][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Ring1][#Branch1][NH1][Ring1][#Branch2],\"2-[3-[(2,3-dichloro4h-thieno[2,3-d]pyrrole-5-carbonyl)amino]-2-oxo-3,4-dihydroquinolin-1-yl]acetic acid\",0.67\nCC(C)n1c2ccccc2c3c(C)c(NC(=O)N4CCOCC4)ccc13,\"InChI=1S/C21H25N3O2/c1-14(2)24-18-7-5-4-6-16(18)20-15(3)17(8-9-19(20)24)22-21(25)23-10-12-26-13-11-23/h4-9,14H,10-13H2,1-3H3,(H,22,25)\",[C][C][Branch1][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Branch1][C][C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][#Branch1][Ring1][S],n-(4-methyl-9-propan-2-ylcarbazol-3-yl)morpholine-4-carboxamide,3.5\nFc1ccccc1c2ccc3c(c2)C(=O)C(=O)c4ccccc34,InChI=1S/C20H11FO2/c21-18-8-4-3-5-13(18)12-9-10-15-14-6-1-2-7-16(14)19(22)20(23)17(15)11-12/h1-11H,[F][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"2-(2-fluorophenyl)phenanthrene-9,10-dione\",2.92\nO=S(=O)(Nc1ccc(cc1)S(=O)(=O)Nc2nccs2)c3ccc4OCCOc4c3,\"InChI=1S/C17H15N3O6S3/c21-28(22,20-17-18-7-10-27-17)13-3-1-12(2-4-13)19-29(23,24)14-5-6-15-16(11-14)26-9-8-25-15/h1-7,10-11,19H,8-9H2,(H,18,20)\",[O][=S][=Branch1][C][=O][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1][C][=C][C][=C][O][C][C][O][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"n-[4-(1,3-thiazol-2-ylsulfamoyl)phenyl]-2,3-dihydro-1,4-benzodioxine-7-sulfonamide\",1.97\nCOc1ccc(cc1)C(CNC(=O)Nc2ccccc2)N3CCN(C)CC3,\"InChI=1S/C21H28N4O2/c1-24-12-14-25(15-13-24)20(17-8-10-19(27-2)11-9-17)16-22-21(26)23-18-6-4-3-5-7-18/h3-11,20H,12-16H2,1-2H3,(H2,22,23,26)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][S][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],1-[2-(4-methoxyphenyl)-2-(4-methylpiperazin-1-yl)ethyl]-3-phenylurea,1.5\nCOc1ccc(NC(=O)c2ccc(c(C)c2)c3ccncc3)cc1N4CCN(C)CC4,\"InChI=1S/C25H28N4O2/c1-18-16-20(4-6-22(18)19-8-10-26-11-9-19)25(30)27-21-5-7-24(31-3)23(17-21)29-14-12-28(2)13-15-29/h4-11,16-17H,12-15H2,1-3H3,(H,27,30)\",[C][O][C][=C][C][=C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],n-[4-methoxy-3-(4-methylpiperazin-1-yl)phenyl]-3-methyl-4-pyridin-4-ylbenzamide,2.56\nCCOC(=O)C1=Cc2ccc(O)cc2OC1=O,\"InChI=1S/C12H10O5/c1-2-16-11(14)9-5-7-3-4-8(13)6-10(7)17-12(9)15/h3-6,13H,2H2,1H3\",[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O],ethyl 7-hydroxy-2-oxochromene-3-carboxylate,1.2\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OC,\"InChI=1S/C16H13ClFN3O2/c1-22-14-6-10-13(7-15(14)23-2)19-8-20-16(10)21-9-3-4-12(18)11(17)5-9/h3-8H,1-2H3,(H,19,20,21)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C],\"n-(3-chloro-4-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine\",3.67\nOC(=O)COc1ccc(cc1c2ccccc2)[N+](=O)[O-],\"InChI=1S/C14H11NO5/c16-14(17)9-20-13-7-6-11(15(18)19)8-12(13)10-4-2-1-3-5-10/h1-8H,9H2,(H,16,17)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1],2-(4-nitro-2-phenylphenoxy)acetic acid,-0.69\nNc1ncnc(Nc2ccccc2)n1,\"InChI=1S/C9H9N5/c10-8-11-6-12-9(14-8)13-7-4-2-1-3-5-7/h1-6H,(H3,10,11,12,13,14)\",[N][C][=N][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N],\"n-phenyl-1,3,5-triazine-2,4-diamine\",1.4\nCCN(CC)CCOc1ccc(cc1)\\C(=C(\\Cl)/c2ccccc2)\\c3ccccc3,\"InChI=1S/C26H28ClNO/c1-3-28(4-2)19-20-29-24-17-15-22(16-18-24)25(21-11-7-5-8-12-21)26(27)23-13-9-6-10-14-23/h5-18H,3-4,19-20H2,1-2H3/b26-25+\",[C][C][N][Branch1][Ring1][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][\\C][=Branch1][=N][=C][Branch1][C][\\Cl][/C][=C][C][=C][C][=C][Ring1][=Branch1][\\C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[4-[(e)-2-chloro-1,2-di(phenyl)ethenyl]phenoxy]-n,n-diethylethanamine\",4.09\nCOc1cc(O)c2C(=O)O[C@@H](C)C\\C=C/C(=O)[C@@H](O)[C@@H](O)C\\C=C\\c2c1,\"InChI=1S/C19H22O7/c1-11-5-3-7-14(20)18(23)15(21)8-4-6-12-9-13(25-2)10-16(22)17(12)19(24)26-11/h3-4,6-7,9-11,15,18,21-23H,5,8H2,1-2H3/b6-4+,7-3-/t11-,15-,18+/m0/s1\",[C][O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][O][C@@H1][Branch1][C][C][C][\\C][=C][/C][=Branch1][C][=O][C@@H1][Branch1][C][O][C@@H1][Branch1][C][O][C][\\C][=C][\\C][Ring2][Ring1][Ring1][=C][Ring2][Ring1][Branch2],\"(2e,5s,6s,8z,11s)-5,6,15-trihydroxy-17-methoxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(14),2,8,15,17-pentaene-7,13-dione\",1.64\nCCN1N(C2CCCC2)c3nc(Nc4ccc(cc4OC)C(=O)NC5CCN(C)CC5)ncc3N(C)C1=O,\"InChI=1S/C27H38N8O3/c1-5-34-27(37)33(3)22-17-28-26(31-24(22)35(34)20-8-6-7-9-20)30-21-11-10-18(16-23(21)38-4)25(36)29-19-12-14-32(2)15-13-19/h10-11,16-17,19-20H,5-9,12-15H2,1-4H3,(H,29,36)(H,28,30,31)\",[C][C][N][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=N][C][Branch2][Ring1][=C][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=N][C][=C][Ring2][Ring1][=Branch2][N][Branch1][C][C][C][Ring2][Ring2][Ring1][=O],\"4-[(1-cyclopentyl-2-ethyl-4-methyl-3-oxopyrimido[5,4-e][1,2,4]triazin-7-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide\",2.75\nCOc1ccccc1Oc2ccc(cc2)N(Cc3cccnc3)S(=O)(=O)CC(F)(F)F,\"InChI=1S/C21H19F3N2O4S/c1-29-19-6-2-3-7-20(19)30-18-10-8-17(9-11-18)26(14-16-5-4-12-25-13-16)31(27,28)15-21(22,23)24/h2-13H,14-15H2,1H3\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][#Branch2][C][C][=C][C][=C][N][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Branch1][C][F][Branch1][C][F][F],\"2,2,2-trifluoro-n-[4-(2-methoxyphenoxy)phenyl]-n-(pyridin-3-ylmethyl)ethanesulfonamide\",1.5\nCC1=NC(=C(NC1=O)c2ccccc2)c3ccc(CN4CCC(CC4)N5C(=O)Nc6ccccc56)cc3,\"InChI=1S/C30H29N5O2/c1-20-29(36)33-28(22-7-3-2-4-8-22)27(31-20)23-13-11-21(12-14-23)19-34-17-15-24(16-18-34)35-26-10-6-5-9-25(26)32-30(35)37/h2-14,24H,15-19H2,1H3,(H,32,37)(H,33,36)\",[C][C][=N][C][=Branch1][P][=C][Branch1][=Branch1][N][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][N][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1],3-[1-[[4-(6-methyl-5-oxo-3-phenyl-4h-pyrazin-2-yl)phenyl]methyl]piperidin-4-yl]-1h-benzimidazol-2-one,3.8\nClc1ccc(N2CCN(CC2)C(=O)COCc3ccccn3)c(Cl)c1,\"InChI=1S/C18H19Cl2N3O2/c19-14-4-5-17(16(20)11-14)22-7-9-23(10-8-22)18(24)13-25-12-15-3-1-2-6-21-15/h1-6,11H,7-10,12-13H2\",[Cl][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2],\"1-[4-(2,4-dichlorophenyl)piperazin-1-yl]-2-(pyridin-2-ylmethoxy)ethanone\",3.47\nCOc1ccc(cc1)N2Sc3ccccc3C2=O,\"InChI=1S/C14H11NO2S/c1-17-11-8-6-10(7-9-11)15-14(16)12-4-2-3-5-13(12)18-15/h2-9H,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][S][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O],\"2-(4-methoxyphenyl)-1,2-benzothiazol-3-one\",3.02\nCN1C[C@H](c2ccccc2)c3cccc(N)c3C1,\"InChI=1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3/t14-/m1/s1\",[C][N][C][C@H1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1][C][Ring1][P],\"(4r)-2-methyl-4-phenyl-3,4-dihydro-1h-isoquinolin-8-amine\",2.11\nCC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)C(=O)N4CC[C@@H](C4)N(C)C)ncc2F,\"InChI=1S/C24H30FN7O/c1-15(2)32-16(3)26-13-21(32)22-20(25)12-27-24(29-22)28-18-8-6-17(7-9-18)23(33)31-11-10-19(14-31)30(4)5/h6-9,12-13,15,19H,10-11,14H2,1-5H3,(H,27,28,29)/t19-/m0/s1\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][=C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][Ring2][C][Ring1][Branch1][N][Branch1][C][C][C][=N][C][=C][Ring2][Ring1][#Branch1][F],[(3s)-3-dimethylaminopyrrolidin-1-yl]-[4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]methanone,2.16\nCOc1cc(ccc1Cn2cnc3ccc(NC(=O)CC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5,\"InChI=1S/C29H30N4O5S/c1-38-27-16-21(29(35)32-39(36,37)24-9-3-2-4-10-24)11-12-22(27)18-33-19-30-25-14-13-23(17-26(25)33)31-28(34)15-20-7-5-6-8-20/h2-4,9-14,16-17,19-20H,5-8,15,18H2,1H3,(H,31,34)(H,32,35)\",[C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][C][=N][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],4-[[6-[(2-cyclopentylacetyl)amino]benzimidazol-1-yl]methyl]-3-methoxy-n-phenylsulfonylbenzamide,0.9\nNC(=N)c1cc2c(I)cccc2s1,\"InChI=1S/C9H7IN2S/c10-6-2-1-3-7-5(6)4-8(13-7)9(11)12/h1-4H,(H3,11,12)\",[N][C][=Branch1][C][=N][C][=C][C][=C][Branch1][C][I][C][=C][C][=C][Ring1][#Branch1][S][Ring1][#Branch2],4-iodo-1-benzothiophene-2-carboximidamide,0.74\nOc1ccc(cc1)C2=CC(=O)c3ccccc3N2,\"InChI=1S/C15H11NO2/c17-11-7-5-10(6-8-11)14-9-15(18)12-3-1-2-4-13(12)16-14/h1-9,17H,(H,16,18)\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O],2-(4-hydroxyphenyl)-1h-quinolin-4-one,2.34\nCN(C)N(C)C(=O)[C@@]1(Cc2ccccc2)CCCN(C1)C(=O)[C@@H](Cc3c[nH]c4ccccc34)NC(=O)C(C)(C)N,\"InChI=1S/C31H42N6O3/c1-30(2,32)28(39)34-26(18-23-20-33-25-15-10-9-14-24(23)25)27(38)37-17-11-16-31(21-37,29(40)36(5)35(3)4)19-22-12-7-6-8-13-22/h6-10,12-15,20,26,33H,11,16-19,21,32H2,1-5H3,(H,34,39)/t26-,31-/m1/s1\",[C][N][Branch1][C][C][N][Branch1][C][C][C][=Branch1][C][=O][C@@][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][N][Branch1][Ring2][C][Ring1][=N][C][=Branch1][C][=O][C@@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][N],2-amino-n-[(2r)-1-[(3r)-3-(dimethylamino-methylcarbamoyl)-3-(phenylmethyl)piperidin-1-yl]-3-(1h-indol-3-yl)-1-oxopropan-2-yl]-2-methylpropanamide,2.1\nCc1nc(Nc2ncc(s2)C(=O)Nc3c(C)cccc3Cl)cc(n1)N4CCN(CCO)CC4,\"InChI=1S/C22H26ClN7O2S/c1-14-4-3-5-16(23)20(14)28-21(32)17-13-24-22(33-17)27-18-12-19(26-15(2)25-18)30-8-6-29(7-9-30)10-11-31/h3-5,12-13,31H,6-11H2,1-2H3,(H,28,32)(H,24,25,26,27)\",[C][C][=N][C][Branch2][Ring1][N][N][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][Cl][=C][C][=Branch1][Branch1][=N][Ring2][Ring1][#Branch1][N][C][C][N][Branch1][Ring2][C][C][O][C][C][Ring1][=Branch2],\"n-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-1,3-thiazole-5-carboxamide\",3.41\nNc1ncnc2c1ncn2Cc3ccccc3,\"InChI=1S/C12H11N5/c13-11-10-12(15-7-14-11)17(8-16-10)6-9-4-2-1-3-5-9/h1-5,7-8H,6H2,(H2,13,14,15)\",[N][C][=N][C][=N][C][=C][Ring1][=Branch1][N][=C][N][Ring1][Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],9-(phenylmethyl)purin-6-amine,1.53\nCC(C)OC(=O)N1CCC(CC1)Oc2ncnc(Oc3ccc(cc3F)S(=O)(=O)C)c2C,\"InChI=1S/C21H26FN3O6S/c1-13(2)29-21(26)25-9-7-15(8-10-25)30-19-14(3)20(24-12-23-19)31-18-6-5-16(11-17(18)22)32(4,27)28/h5-6,11-13,15H,7-10H2,1-4H3\",[C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][Branch2][Ring1][Branch1][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Ring2][Ring1][C][C],propan-2-yl 4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate,3.7\nNc1c(cnn1c2ccc(F)cc2)C(=O)c3cccc(OC[C@@H](O)CO)c3,\"InChI=1S/C19H18FN3O4/c20-13-4-6-14(7-5-13)23-19(21)17(9-22-23)18(26)12-2-1-3-16(8-12)27-11-15(25)10-24/h1-9,15,24-25H,10-11,21H2/t15-/m0/s1\",[N][C][=C][Branch1][P][C][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][=Branch2][O][C][C@@H1][Branch1][C][O][C][O][=C][Ring1][N],\"[5-amino-1-(4-fluorophenyl)pyrazol-4-yl]-[3-[(2s)-2,3-dihydroxypropoxy]phenyl]methanone\",1.91\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2cccc(c2)C(=O)O)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C28H26F3N3O7/c1-16(2)23(24(36)28(29,30)31)33-22(35)14-34-21(18-9-6-10-19(13-18)26(38)39)12-11-20(25(34)37)32-27(40)41-15-17-7-4-3-5-8-17/h3-13,16,23H,14-15H2,1-2H3,(H,32,40)(H,33,35)(H,38,39)\",[C][C][Branch1][C][C][C][Branch2][Branch1][Ring1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][Branch1][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"3-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-5-(phenylmethoxycarbonylamino)pyridin-2-yl]benzoic acid\",1.2\nCc1ccc(cc1)C(=O)c2ccc(CC(=O)O)n2C,\"InChI=1S/C15H15NO3/c1-10-3-5-11(6-4-10)15(19)13-8-7-12(16(13)2)9-14(17)18/h3-8H,9H2,1-2H3,(H,17,18)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][Ring1][=Branch2][C],2-[1-methyl-5-(4-methylbenzoyl)pyrrol-2-yl]acetic acid,-1.02\nCOc1cc(ccc1Cc2c[nH]c3ccc(NC(=O)CC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5C,\"InChI=1S/C31H33N3O5S/c1-20-7-3-6-10-29(20)40(37,38)34-31(36)23-12-11-22(28(17-23)39-2)16-24-19-32-27-14-13-25(18-26(24)27)33-30(35)15-21-8-4-5-9-21/h3,6-7,10-14,17-19,21,32H,4-5,8-9,15-16H2,1-2H3,(H,33,35)(H,34,36)\",[C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][C][=C][NH1][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C],4-[[5-[(2-cyclopentylacetyl)amino]-1h-indol-3-yl]methyl]-3-methoxy-n-(2-methylphenyl)sulfonylbenzamide,2\nCOc1cc2ncnc(Nc3ccc(F)cc3)c2cc1OC,\"InChI=1S/C16H14FN3O2/c1-21-14-7-12-13(8-15(14)22-2)18-9-19-16(12)20-11-5-3-10(17)4-6-11/h3-9H,1-2H3,(H,18,19,20)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=N][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][=C][Ring1][=C][C][=C][Ring2][Ring1][C][O][C],\"n-(4-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine\",3.1\nCOc1ccccc1CNC(=O)c2ccc3cnccc3n2,\"InChI=1S/C17H15N3O2/c1-22-16-5-3-2-4-13(16)11-19-17(21)15-7-6-12-10-18-9-8-14(12)20-15/h2-10H,11H2,1H3,(H,19,21)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2],\"n-[(2-methoxyphenyl)methyl]-1,6-naphthyridine-2-carboxamide\",1.8\nCCN(CC)CCOc1ccc(cc1)C(O)(Cc2ccc(Cl)cc2)c3ccc(C)cc3,\"InChI=1S/C27H32ClNO2/c1-4-29(5-2)18-19-31-26-16-12-24(13-17-26)27(30,23-10-6-21(3)7-11-23)20-22-8-14-25(28)15-9-22/h6-17,30H,4-5,18-20H2,1-3H3\",[C][C][N][Branch1][Ring1][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1],2-(4-chlorophenyl)-1-[4-(2-diethylaminoethoxy)phenyl]-1-(4-methylphenyl)ethanol,3.98\nClc1ccccc1C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C18H22ClNO/c19-16-4-2-1-3-15(16)17(21)20-11-18-8-12-5-13(9-18)7-14(6-12)10-18/h1-4,12-14H,5-11H2,(H,20,21)\",[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chlorobenzamide,4.05\nNc1nccc(n1)c2cccs2,\"InChI=1S/C8H7N3S/c9-8-10-4-3-6(11-8)7-2-1-5-12-7/h1-5H,(H2,9,10,11)\",[N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][S][Ring1][Branch1],4-thiophen-2-ylpyrimidin-2-amine,1.75\nCOc1cc2ncc(C(=O)N)c(Nc3cccc(Cl)c3Cl)c2cc1OC,\"InChI=1S/C18H15Cl2N3O3/c1-25-14-6-9-13(7-15(14)26-2)22-8-10(18(21)24)17(9)23-12-5-3-4-11(19)16(12)20/h3-8H,1-2H3,(H2,21,24)(H,22,23)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C],\"4-[(2,3-dichlorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",3.4\nCN(C)c1ccc2N=C3C=CC(=[N+](C)C)C=C3Sc2c1,\"InChI=1S/C16H18N3S/c1-18(2)11-5-7-13-15(9-11)20-16-10-12(19(3)4)6-8-14(16)17-13/h5-10H,1-4H3/q+1\",[C][N][Branch1][C][C][C][=C][C][=C][N][=C][C][=C][C][=Branch1][=Branch1][=N+1][Branch1][C][C][C][C][=C][Ring1][=Branch2][S][C][Ring1][=N][=C][Ring1][P],(7-dimethylaminophenothiazin-3-ylidene)-dimethylazanium,-0.88\nCC[C@H](NC(=O)c1c(CS(=O)(=O)C)c(nc2ccccc12)c3ccccc3)c4ccccc4,\"InChI=1S/C27H26N2O3S/c1-3-23(19-12-6-4-7-13-19)29-27(30)25-21-16-10-11-17-24(21)28-26(20-14-8-5-9-15-20)22(25)18-33(2,31)32/h4-17,23H,3,18H2,1-2H3,(H,29,30)/t23-/m0/s1\",[C][C][C@H1][Branch2][Ring2][=Branch2][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch2][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-(methylsulfonylmethyl)-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,3.25\nCC(C)NCC(O)COc1ccc(CCOCC2CC2)cc1,\"InChI=1S/C18H29NO3/c1-14(2)19-11-17(20)13-22-18-7-5-15(6-8-18)9-10-21-12-16-3-4-16/h5-8,14,16-17,19-20H,3-4,9-13H2,1-2H3\",[C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][C][C][O][C][C][C][C][Ring1][Ring1][C][=C][Ring1][=N],1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-(propan-2-ylamino)propan-2-ol,0.63\nO=C(NCC12CC3CC(CC(C3)C1)C2)c4ccccc4,\"InChI=1S/C18H23NO/c20-17(16-4-2-1-3-5-16)19-12-18-9-13-6-14(10-18)8-15(7-13)11-18/h1-5,13-15H,6-12H2,(H,19,20)\",[O][=C][Branch2][Ring1][#Branch1][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],n-(1-adamantylmethyl)benzamide,4.21\nCc1ccn2c(NC(=O)c3ccccc3)c(nc2c1)c4cccs4,\"InChI=1S/C19H15N3OS/c1-13-9-10-22-16(12-13)20-17(15-8-5-11-24-15)18(22)21-19(23)14-6-3-2-4-7-14/h2-12H,1H3,(H,21,23)\",[C][C][C][=C][N][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][=Branch2][N][=C][Ring1][=C][C][=Ring2][Ring1][C][C][=C][C][=C][S][Ring1][Branch1],\"n-(7-methyl-2-thiophen-2-ylimidazo[3,2-a]pyridin-3-yl)benzamide\",2.87\nFc1cc(ccc1C2=CCOCC2)N3C[C@H](COc4ccon4)OC3=O,\"InChI=1S/C18H17FN2O5/c19-16-9-13(1-2-15(16)12-3-6-23-7-4-12)21-10-14(26-18(21)22)11-24-17-5-8-25-20-17/h1-3,5,8-9,14H,4,6-7,10-11H2/t14-/m1/s1\",[F][C][=C][C][=Branch1][=C][=C][C][=C][Ring1][=Branch1][C][=C][C][O][C][C][Ring1][=Branch1][N][C][C@H1][Branch1][#Branch2][C][O][C][C][=C][O][N][=Ring1][Branch1][O][C][Ring1][N][=O],\"(5r)-3-[4-(3,6-dihydro-2h-pyran-4-yl)-3-fluorophenyl]-5-(1,2-oxazol-3-yloxymethyl)-1,3-oxazolidin-2-one\",2.61\nCC(C)(C)NC(=O)[C@@H]1CN(Cc2cccnc2)CCN1C[C@@H](O)C[C@@H](Cc3ccccc3)C(=O)N[C@@H]4[C@H](O)Cc5ccccc45,\"InChI=1S/C36H47N5O4/c1-36(2,3)39-35(45)31-24-40(22-26-12-9-15-37-21-26)16-17-41(31)23-29(42)19-28(18-25-10-5-4-6-11-25)34(44)38-33-30-14-8-7-13-27(30)20-32(33)43/h4-15,21,28-29,31-33,42-43H,16-20,22-24H2,1-3H3,(H,38,44)(H,39,45)/t28-,29+,31+,32-,33+/m1/s1\",[C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][C@@H1][C][N][Branch1][#Branch2][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][C][N][Ring1][=N][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@@H1][C@H1][Branch1][C][O][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"(2s)-n-tert-butyl-1-[(2s,4r)-2-hydroxy-5-[[(1s,2r)-2-hydroxy-2,3-dihydro-1h-inden-1-yl]amino]-5-oxo-4-(phenylmethyl)pentyl]-4-(pyridin-3-ylmethyl)piperazine-2-carboxamide\",2.9\nCC(=O)Nc1ccc(O)cc1,\"InChI=1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],n-(4-hydroxyphenyl)acetamide,0.25\nCc1cc(NCc2ccccc2)nc3ccccc13,\"InChI=1S/C17H16N2/c1-13-11-17(18-12-14-7-3-2-4-8-14)19-16-10-6-5-9-15(13)16/h2-11H,12H2,1H3,(H,18,19)\",[C][C][=C][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1],4-methyl-n-(phenylmethyl)quinolin-2-amine,3.69\nNC(=O)Nc1sc(cc1C(=O)N[C@H]2CCCNC2)c3cc(F)cc(F)c3,\"InChI=1S/C17H18F2N4O2S/c18-10-4-9(5-11(19)6-10)14-7-13(16(26-14)23-17(20)25)15(24)22-12-2-1-3-21-8-12/h4-7,12,21H,1-3,8H2,(H,22,24)(H3,20,23,25)/t12-/m0/s1\",[N][C][=Branch1][C][=O][N][C][S][C][=Branch2][Ring1][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2],\"2-(carbamoylamino)-5-(3,5-difluorophenyl)-n-[(3s)-piperidin-3-yl]thiophene-3-carboxamide\",2.18\nCOc1ccc(cc1)c2cc(ccc2OCC(=O)O)C(F)(F)F,\"InChI=1S/C16H13F3O4/c1-22-12-5-2-10(3-6-12)13-8-11(16(17,18)19)4-7-14(13)23-9-15(20)21/h2-8H,9H2,1H3,(H,20,21)\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=N][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F],2-[2-(4-methoxyphenyl)-4-(trifluoromethyl)phenoxy]acetic acid,0.29\nNc1ccccc1NC(=O)c2ccccn2,\"InChI=1S/C12H11N3O/c13-9-5-1-2-6-10(9)15-12(16)11-7-3-4-8-14-11/h1-8H,13H2,(H,15,16)\",[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=N][Ring1][=Branch1],n-(2-aminophenyl)pyridine-2-carboxamide,1\nO=C(Nc1nccs1)c2cccnc2,\"InChI=1S/C9H7N3OS/c13-8(7-2-1-3-10-6-7)12-9-11-4-5-14-9/h1-6H,(H,11,12,13)\",[O][=C][Branch1][=Branch2][N][C][=N][C][=C][S][Ring1][Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],\"n-(1,3-thiazol-2-yl)pyridine-3-carboxamide\",2.25\nNc1nc(nc(N)c1Cc2ccccc2F)c3ccccn3,\"InChI=1S/C16H14FN5/c17-12-6-2-1-5-10(12)9-11-14(18)21-16(22-15(11)19)13-7-3-4-8-20-13/h1-8H,9H2,(H4,18,19,21,22)\",[N][C][=N][C][=Branch2][Ring1][Ring1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][=C][C][=N][Ring1][=Branch1],\"5-[(2-fluorophenyl)methyl]-2-pyridin-2-ylpyrimidine-4,6-diamine\",2.12\nFC(F)(F)c1nnc2ccc(nn12)N3CCCC3,\"InChI=1S/C10H10F3N5/c11-10(12,13)9-15-14-7-3-4-8(16-18(7)9)17-5-1-2-6-17/h3-4H,1-2,5-6H2\",[F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][C][C][C][Ring1][Branch1],\"6-pyrrolidin-1-yl-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\",2.41\nc1ccc2ccccc2c1,InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H,[C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],naphthalene,3.29\nCc1onc(CO)c1C(=O)Nc2nccs2,\"InChI=1S/C9H9N3O3S/c1-5-7(6(4-13)12-15-5)8(14)11-9-10-2-3-16-9/h2-3,13H,4H2,1H3,(H,10,11,14)\",[C][C][O][N][=C][Branch1][Ring1][C][O][C][=Ring1][#Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"3-(hydroxymethyl)-5-methyl-n-(1,3-thiazol-2-yl)-1,2-oxazole-4-carboxamide\",1.53\nCc1ccnc(NCc2c(O)ccc3ccccc23)c1,\"InChI=1S/C17H16N2O/c1-12-8-9-18-17(10-12)19-11-15-14-5-3-2-4-13(14)6-7-16(15)20/h2-10,20H,11H2,1H3,(H,18,19)\",[C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][C][=C][Branch1][C][O][C][=C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][=C][Ring2][Ring1][Ring1],1-[[(4-methylpyridin-2-yl)amino]methyl]naphthalen-2-ol,4.24\nCC(C)CN1C(=O)N(C)C(=O)c2c1nn(Cc3cccc4ccccc34)c2c5ccncc5,\"InChI=1S/C26H25N5O2/c1-17(2)15-30-24-22(25(32)29(3)26(30)33)23(19-11-13-27-14-12-19)31(28-24)16-20-9-6-8-18-7-4-5-10-21(18)20/h4-14,17H,15-16H2,1-3H3\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][C][Ring1][=Branch2][=N][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Ring1][S][C][=C][C][=N][C][=C][Ring1][=Branch1],\"5-methyl-7-(2-methylpropyl)-2-(naphthalen-1-ylmethyl)-3-pyridin-4-ylpyrazolo[4,3-e]pyrimidine-4,6-dione\",4.3\nCNC(=O)c1ccc(Nc2ncc(F)c(n2)c3cnc(C)n3C(C)C)cc1F,\"InChI=1S/C19H20F2N6O/c1-10(2)27-11(3)23-9-16(27)17-15(21)8-24-19(26-17)25-12-5-6-13(14(20)7-12)18(28)22-4/h5-10H,1-4H3,(H,22,28)(H,24,25,26)\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][F][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][#Branch1][F],2-fluoro-4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-methylbenzamide,3.31\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN4CCCCC4,\"InChI=1S/C23H26ClFN4O2/c1-30-21-14-20-17(13-22(21)31-11-5-10-29-8-3-2-4-9-29)23(27-15-26-20)28-16-6-7-19(25)18(24)12-16/h6-7,12-15H,2-5,8-11H2,1H3,(H,26,27,28)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][C][C][C][C][C][Ring1][=Branch1],n-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-piperidin-1-ylpropoxy)quinazolin-4-amine,3.3\nNCCCC(=O)OCCN1CCN(CCCN2c3ccccc3Sc4ccc(Cl)cc24)CC1,\"InChI=1S/C25H33ClN4O2S/c26-20-8-9-24-22(19-20)30(21-5-1-2-6-23(21)33-24)12-4-11-28-13-15-29(16-14-28)17-18-32-25(31)7-3-10-27/h1-2,5-6,8-9,19H,3-4,7,10-18,27H2\",[N][C][C][C][C][=Branch1][C][=O][O][C][C][N][C][C][N][Branch2][Ring1][O][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1][C][C][Ring2][Ring1][Branch2],2-[4-[3-(2-chlorophenothiazin-10-yl)propyl]piperazin-1-yl]ethyl 4-aminobutanoate,1.5\nCC(C)NC[C@@H](O)COc1cccc2ccccc12,\"InChI=1S/C16H21NO2/c1-12(2)17-10-14(18)11-19-16-9-5-7-13-6-3-4-8-15(13)16/h3-9,12,14,17-18H,10-11H2,1-2H3/t14-/m1/s1\",[C][C][Branch1][C][C][N][C][C@@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],(2r)-1-naphthalen-1-yloxy-3-(propan-2-ylamino)propan-2-ol,1.13\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3ccc(cc3)C(=O)O)C(=O)C(F)(F)F,\"InChI=1S/C28H26F3N3O7/c1-16(2)23(24(36)28(29,30)31)33-22(35)14-34-21(18-6-4-3-5-7-18)13-12-20(25(34)37)32-27(40)41-15-17-8-10-19(11-9-17)26(38)39/h3-13,16,23H,14-15H2,1-2H3,(H,32,40)(H,33,35)(H,38,39)\",[C][C][Branch1][C][C][C][Branch2][Branch1][C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"4-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamoyloxymethyl]benzoic acid\",0.84\nCc1nc(CSc2ccc(Cl)cc2)cc(n1)N3CCOCC3,\"InChI=1S/C16H18ClN3OS/c1-12-18-14(11-22-15-4-2-13(17)3-5-15)10-16(19-12)20-6-8-21-9-7-20/h2-5,10H,6-9,11H2,1H3\",[C][C][=N][C][Branch1][=C][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][C][=Branch1][Ring2][=N][Ring1][#C][N][C][C][O][C][C][Ring1][=Branch1],4-[(4-chlorophenyl)sulfanylmethyl]-2-methyl-6-morpholin-4-ylpyrimidine,3.38\nClc1ccc(cc1Cl)[C@]23CNC[C@H]2C3,\"InChI=1S/C11H11Cl2N/c12-9-2-1-7(3-10(9)13)11-4-8(11)5-14-6-11/h1-3,8,14H,4-6H2/t8-,11+/m1/s1\",[Cl][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C@][C][N][C][C@H1][Ring1][Branch1][C][Ring1][=Branch1],\"(1r,5s)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane\",1.96\nFc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)NCc3ccccc3,\"InChI=1S/C20H21FN2O2/c21-18-8-6-16(7-9-18)19(24)17-10-12-23(13-11-17)20(25)22-14-15-4-2-1-3-5-15/h1-9,17H,10-14H2,(H,22,25)\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],4-(4-fluorobenzoyl)-n-(phenylmethyl)piperidine-1-carboxamide,3.15\nClc1ccccc1N2CCN(CC2)C(=O)NC3CCCCC3,\"InChI=1S/C17H24ClN3O/c18-15-8-4-5-9-16(15)20-10-12-21(13-11-20)17(22)19-14-6-2-1-3-7-14/h4-5,8-9,14H,1-3,6-7,10-13H2,(H,19,22)\",[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1],4-(2-chlorophenyl)-n-cyclohexylpiperazine-1-carboxamide,3.78\nCOc1cc(OC)c(cc1NC(=O)C)S(=O)(=O)N2C(C)Cc3ccccc23,\"InChI=1S/C19H22N2O5S/c1-12-9-14-7-5-6-8-16(14)21(12)27(23,24)19-10-15(20-13(2)22)17(25-3)11-18(19)26-4/h5-8,10-12H,9H2,1-4H3,(H,20,22)\",[C][O][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][O][C][=C][Ring1][Branch2][N][C][=Branch1][C][=O][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"n-[2,4-dimethoxy-5-[(2-methyl-2,3-dihydroindol-1-yl)sulfonyl]phenyl]acetamide\",1.95\nO=C1Nc2ccc(cc2C1=O)S(=O)(=O)N3CCC[C@H]3COc4ccccc4,\"InChI=1S/C19H18N2O5S/c22-18-16-11-15(8-9-17(16)20-19(18)23)27(24,25)21-10-4-5-13(21)12-26-14-6-2-1-3-7-14/h1-3,6-9,11,13H,4-5,10,12H2,(H,20,22,23)/t13-/m0/s1\",[O][=C][N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C@H1][Ring1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-[(2s)-2-(phenoxymethyl)pyrrolidin-1-yl]sulfonyl-1h-indole-2,3-dione\",2.7\nOc1ccc(CCc2ccc(O)cc2)cc1,\"InChI=1S/C14H14O2/c15-13-7-3-11(4-8-13)1-2-12-5-9-14(16)10-6-12/h3-10,15-16H,1-2H2\",[O][C][=C][C][=C][Branch1][=C][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][Ring1][#C],4-[2-(4-hydroxyphenyl)ethyl]phenol,3.3\nCCO[C@@H]1OC(=O)C[C@@H]1NC(=O)[C@@H]2CCCN3N2C(=O)[C@H](CCC3=O)NC(=O)c4nccc5ccccc45,\"InChI=1S/C26H29N5O7/c1-2-37-26-18(14-21(33)38-26)29-23(34)19-8-5-13-30-20(32)10-9-17(25(36)31(19)30)28-24(35)22-16-7-4-3-6-15(16)11-12-27-22/h3-4,6-7,11-12,17-19,26H,2,5,8-10,13-14H2,1H3,(H,28,35)(H,29,34)/t17-,18-,19-,26+/m0/s1\",[C][C][O][C@@H1][O][C][=Branch1][C][=O][C][C@@H1][Ring1][=Branch1][N][C][=Branch1][C][=O][C@@H1][C][C][C][N][N][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][C][Ring1][Branch2][=O][N][C][=Branch1][C][=O][C][=N][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"(1s,9s)-n-[(2r,3s)-2-ethoxy-5-oxooxolan-3-yl]-9-(isoquinoline-1-carbonylamino)-6,10-dioxo-2,3,4,7,8,9-hexahydro-1h-pyridazino[1,2-a]diazepine-1-carboxamide\",1.16\nCC(C)(C)NC[C@H](O)COc1nsnc1N2CCOCC2,\"InChI=1S/C13H24N4O3S/c1-13(2,3)14-8-10(18)9-20-12-11(15-21-16-12)17-4-6-19-7-5-17/h10,14,18H,4-9H2,1-3H3/t10-/m0/s1\",[C][C][Branch1][C][C][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][O][C][=N][S][N][=C][Ring1][Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"(2s)-1-(tert-butylamino)-3-[(4-morpholin-4-yl-1,2,5-thiadiazol-3-yl)oxy]propan-2-ol\",-0.22\nCN(C(CN1CCCC1)c2ccccc2)C(=O)Cc3ccc(Cl)c(Cl)c3,\"InChI=1S/C21H24Cl2N2O/c1-24(21(26)14-16-9-10-18(22)19(23)13-16)20(15-25-11-5-6-12-25)17-7-3-2-4-8-17/h2-4,7-10,13,20H,5-6,11-12,14-15H2,1H3\",[C][N][Branch2][Ring1][Ring2][C][Branch1][=Branch2][C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"2-(3,4-dichlorophenyl)-n-methyl-n-(1-phenyl-2-pyrrolidin-1-ylethyl)acetamide\",3.38\n[O-][N+](=O)c1ccc2NC(=O)CN=C(c3ccccc3Cl)c2c1,\"InChI=1S/C15H10ClN3O3/c16-12-4-2-1-3-10(12)15-11-7-9(19(21)22)5-6-13(11)18-14(20)8-17-15/h1-7H,8H2,(H,18,20)\",[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][N][C][=Branch1][C][=O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][Ring1][#C][=C][Ring2][Ring1][Ring1],\"5-(2-chlorophenyl)-7-nitro-1,3-dihydro-1,4-benzodiazepin-2-one\",3.72\nCN(CCCc1ccccc1)S(=O)(=O)c2cc(C(=O)N3CCc4ccc(cc4C3)S(=O)(=O)NCCc5ccccc5)c(O)c(O)c2O,\"InChI=1S/C34H37N3O8S2/c1-36(19-8-13-24-9-4-2-5-10-24)47(44,45)30-22-29(31(38)33(40)32(30)39)34(41)37-20-17-26-14-15-28(21-27(26)23-37)46(42,43)35-18-16-25-11-6-3-7-12-25/h2-7,9-12,14-15,21-22,35,38-40H,8,13,16-20,23H2,1H3\",[C][N][Branch1][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch2][Ring2][#Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring2][Ring1][S][O],\"n-(2-phenylethyl)-2-[2,3,4-trihydroxy-5-(methyl-(3-phenylpropyl)sulfamoyl)benzoyl]-3,4-dihydro-1h-isoquinoline-7-sulfonamide\",0.75\nCCCNC(=O)c1nnc2c(cccc2c1N)c3cnc(OC)nc3OC,\"InChI=1S/C18H20N6O3/c1-4-8-20-16(25)15-13(19)11-7-5-6-10(14(11)23-24-15)12-9-21-18(27-3)22-17(12)26-2/h5-7,9H,4,8H2,1-3H3,(H2,19,23)(H,20,25)\",[C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][N][=C][Branch1][Ring1][O][C][N][=C][Ring1][Branch2][O][C],\"4-amino-8-(2,4-dimethoxypyrimidin-5-yl)-n-propylcinnoline-3-carboxamide\",3.26\nNC(=O)c1cc(sc1N)c2ccccc2,\"InChI=1S/C11H10N2OS/c12-10(14)8-6-9(15-11(8)13)7-4-2-1-3-5-7/h1-6H,13H2,(H2,12,14)\",[N][C][=Branch1][C][=O][C][C][=C][Branch1][=Branch1][S][C][=Ring1][Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],2-amino-5-phenylthiophene-3-carboxamide,2.7\nOC1=CC(=O)C2=C(O1)c3ccccc3N(C2=O)c4ccccc4,\"InChI=1S/C18H11NO4/c20-14-10-15(21)23-17-12-8-4-5-9-13(12)19(18(22)16(14)17)11-6-2-1-3-7-11/h1-10,21H\",[O][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Ring2][O][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][Branch1][C][Ring1][O][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-hydroxy-6-phenylpyrano[3,2-c]quinoline-4,5-dione\",0.96\nO=C1NC(=O)c2cc(OCc3ccccc3)ccc12,\"InChI=1S/C15H11NO3/c17-14-12-7-6-11(8-13(12)15(18)16-14)19-9-10-4-2-1-3-5-10/h1-8H,9H2,(H,16,17,18)\",[O][=C][N][C][=Branch1][C][=O][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][C][Ring1][=C],\"5-(phenylmethoxy)isoindole-1,3-dione\",3.1\nClc1cccc(c1)c2cnc3ccc(NC4CCOCC4)nn23,\"InChI=1S/C17H17ClN4O/c18-13-3-1-2-12(10-13)15-11-19-17-5-4-16(21-22(15)17)20-14-6-8-23-9-7-14/h1-5,10-11,14H,6-9H2,(H,20,21)\",[Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][N][=C][C][=C][C][Branch1][#Branch2][N][C][C][C][O][C][C][Ring1][=Branch1][=N][N][Ring1][S][Ring1][=N],\"3-(3-chlorophenyl)-n-(oxan-4-yl)imidazo[2,1-f]pyridazin-6-amine\",4.3\nCOc1ccccc1N2CCN(CCCCNC(=O)c3ccc4ccccc4c3)CC2,\"InChI=1S/C26H31N3O2/c1-31-25-11-5-4-10-24(25)29-18-16-28(17-19-29)15-7-6-14-27-26(30)23-13-12-21-8-2-3-9-22(21)20-23/h2-5,8-13,20H,6-7,14-19H2,1H3,(H,27,30)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch2][Ring1][Branch2][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][C][Ring2][Ring1][#Branch1],n-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]naphthalene-2-carboxamide,3.53\nCC1=C(C(=O)N(C[C@H](N)c2ccccc2)C(=O)N1Cc3c(F)cccc3F)c4ccc5OCOc5c4,\"InChI=1S/C27H23F2N3O4/c1-16-25(18-10-11-23-24(12-18)36-15-35-23)26(33)32(14-22(30)17-6-3-2-4-7-17)27(34)31(16)13-19-20(28)8-5-9-21(19)29/h2-12,22H,13-15,30H2,1H3/t22-/m0/s1\",[C][C][=C][Branch2][Ring2][=Branch2][C][=Branch1][C][=O][N][Branch1][=C][C][C@H1][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][P][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2],\"3-[(2r)-2-amino-2-phenylethyl]-5-(1,3-benzodioxol-5-yl)-1-[(2,6-difluorophenyl)methyl]-6-methylpyrimidine-2,4-dione\",2.67\nOc1ccc(cc1)C2=CC(=O)c3cc(O)ccc3O2,\"InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)15-8-13(18)12-7-11(17)5-6-14(12)19-15/h1-8,16-17H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][O][Ring1][N],6-hydroxy-2-(4-hydroxyphenyl)chromen-4-one,3.3\nONC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C18H15ClN4O4S/c19-14-7-10-6-11(21-17(10)28-14)16(25)20-12-5-9-3-1-2-4-13(9)23(18(12)26)8-15(24)22-27/h1-4,6-7,12,21,27H,5,8H2,(H,20,25)(H,22,24)\",[O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-[2-(hydroxyamino)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",2.4\nCCN1C=C(C(=O)O)C(=O)c2cc(F)c(N3CCNC(C)C3)c(F)c12,\"InChI=1S/C17H19F2N3O3/c1-3-21-8-11(17(24)25)16(23)10-6-12(18)15(13(19)14(10)21)22-5-4-20-9(2)7-22/h6,8-9,20H,3-5,7H2,1-2H3,(H,24,25)\",[C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][Branch1][N][N][C][C][N][C][Branch1][C][C][C][Ring1][#Branch1][C][Branch1][C][F][=C][Ring2][Ring1][#Branch1][Ring1][#C],\"1-ethyl-6,8-difluoro-7-(3-methylpiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid\",-1.1\nO=C1C=COc2ccccc12,InChI=1S/C9H6O2/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H,[O][=C][C][=C][O][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],chromen-4-one,1.4\nCc1nccn1CC2CCc3c(C2=O)c4ccccc4n3C,\"InChI=1S/C18H19N3O/c1-12-19-9-10-21(12)11-13-7-8-16-17(18(13)22)14-5-3-4-6-15(14)20(16)2/h3-6,9-10,13H,7-8,11H2,1-2H3\",[C][C][=N][C][=C][N][Ring1][Branch1][C][C][C][C][C][=C][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O][C],\"9-methyl-3-[(2-methylimidazol-1-yl)methyl]-2,3-dihydro-1h-carbazol-4-one\",1.67\nOc1ccccc1NC(=O)c2cc(ccc2Cl)[N+](=O)[O-],\"InChI=1S/C13H9ClN2O4/c14-10-6-5-8(16(19)20)7-9(10)13(18)15-11-3-1-2-4-12(11)17/h1-7,17H,(H,15,18)\",[O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N+1][=Branch1][C][=O][O-1],2-chloro-n-(2-hydroxyphenyl)-5-nitrobenzamide,2.49\nCCN1CCC[C@H]1CNC(=O)c2cc(ccc2OC)S(=O)(=O)N,\"InChI=1S/C15H23N3O4S/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21)/t11-/m0/s1\",[C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][N],n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2-methoxy-5-sulfamoylbenzamide,-0.84\nCc1cn(C[C@H]2CN(C(=O)O2)c3ccc(C4=CCS(=O)(=O)CC4)c(F)c3)nn1,\"InChI=1S/C18H19FN4O4S/c1-12-9-22(21-20-12)10-15-11-23(18(24)27-15)14-2-3-16(17(19)8-14)13-4-6-28(25,26)7-5-13/h2-4,8-9,15H,5-7,10-11H2,1H3/t15-/m0/s1\",[C][C][=C][N][Branch2][Ring2][=Branch2][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][#C][C][=C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Ring1][Branch2][C][Branch1][C][F][=C][Ring1][#C][N][=N][Ring2][Ring1][O],\"(5r)-3-[4-(1,1-dioxo-3,6-dihydro-2h-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-methyltriazol-1-yl)methyl]-1,3-oxazolidin-2-one\",1.25\nCC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)N4CCN(CC4)C(=O)CO)n2,\"InChI=1S/C23H29N7O2/c1-16(2)30-17(3)25-14-21(30)20-8-9-24-23(27-20)26-18-4-6-19(7-5-18)28-10-12-29(13-11-28)22(32)15-31/h4-9,14,16,31H,10-13,15H2,1-3H3,(H,24,26,27)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][=N][Ring2][Ring1][#Branch1],2-hydroxy-1-[4-[4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]piperazin-1-yl]ethanone,1.69\nCCN1CCC[C@H](C1)C(=O)N2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3,\"InChI=1S/C19H26Cl2N4O2/c1-2-23-7-3-4-14(13-23)18(26)24-8-10-25(11-9-24)19(27)22-15-5-6-16(20)17(21)12-15/h5-6,12,14H,2-4,7-11,13H2,1H3,(H,22,27)/t14-/m1/s1\",[C][C][N][C][C][C][C@H1][Branch1][Ring2][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"n-(3,4-dichlorophenyl)-4-[(3r)-1-ethylpiperidine-3-carbonyl]piperazine-1-carboxamide\",1.6\nCc1ccc(cc1)c2cc(nn2c3ccc(cc3)S(=O)(=O)N)C(F)(F)F,\"InChI=1S/C17H14F3N3O2S/c1-11-2-4-12(5-3-11)15-10-16(17(18,19)20)22-23(15)13-6-8-14(9-7-13)26(21,24)25/h2-10H,1H3,(H2,21,24,25)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch2][Ring1][#Branch1][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][F][Branch1][C][F][F],4-[5-(4-methylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonamide,3.42\nC(Oc1cccc2ccccc12)C3=NCCN3,\"InChI=1S/C14H14N2O/c1-2-6-12-11(4-1)5-3-7-13(12)17-10-14-15-8-9-16-14/h1-7H,8-10H2,(H,15,16)\",[C][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=N][C][C][N][Ring1][Branch1],\"2-(naphthalen-1-yloxymethyl)-4,5-dihydro-1h-imidazole\",0.68\nCCOC(=O)c1ncn2c1CN(C)C(=O)c3cc(F)ccc23,\"InChI=1S/C15H14FN3O3/c1-3-22-15(21)13-12-7-18(2)14(20)10-6-9(16)4-5-11(10)19(12)8-17-13/h4-6,8H,3,7H2,1-2H3\",[C][C][O][C][=Branch1][C][=O][C][N][=C][N][C][=Ring1][Branch1][C][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][=C][Ring1][#Branch1],\"ethyl 8-fluoro-5-methyl-6-oxo-4h-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate\",1.1\nCN1CCc2cc(Cl)c(O)cc2[C@H](C1)c3ccccc3,\"InChI=1S/C17H18ClNO/c1-19-8-7-13-9-16(18)17(20)10-14(13)15(11-19)12-5-3-2-4-6-12/h2-6,9-10,15,20H,7-8,11H2,1H3/t15-/m1/s1\",[C][N][C][C][C][=C][C][Branch1][C][Cl][=C][Branch1][C][O][C][=C][Ring1][Branch2][C@H1][Branch1][Ring2][C][Ring1][=N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(1r)-7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol\",2.5\nCCCCC1=NC2(CCCC2)C(=O)N1Cc3ccc(cc3)c4ccccc4c5nn[nH]n5,\"InChI=1S/C25H28N6O/c1-2-3-10-22-26-25(15-6-7-16-25)24(32)31(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23-27-29-30-28-23/h4-5,8-9,11-14H,2-3,6-7,10,15-17H2,1H3,(H,27,28,29,30)\",[C][C][C][C][C][=N][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][#Branch2][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][=N][NH1][N][=Ring1][Branch1],\"2-butyl-3-[[4-[2-(2h-tetrazol-5-yl)phenyl]phenyl]methyl]-1,3-diazaspiro[4.4]non-1-en-4-one\",1.29\nC1Oc2ccc(Oc3cc(Oc4ccc(cc4)n5ccnc5)ncn3)cc2O1,\"InChI=1S/C20H14N4O4/c1-3-15(4-2-14(1)24-8-7-21-12-24)27-19-10-20(23-11-22-19)28-16-5-6-17-18(9-16)26-13-25-17/h1-12H,13H2\",[C][O][C][=C][C][=C][Branch2][Ring1][S][O][C][=C][C][Branch2][Ring1][Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1][=N][C][=N][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch2][O][Ring2][Ring1][N],\"4-(1,3-benzodioxol-5-yloxy)-6-(4-imidazol-1-ylphenoxy)pyrimidine\",3.17\nO=C1NN=C(Cc2ccccc2)c3ccccc13,\"InChI=1S/C15H12N2O/c18-15-13-9-5-4-8-12(13)14(16-17-15)10-11-6-2-1-3-7-11/h1-9H,10H2,(H,17,18)\",[O][=C][N][N][=C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1],4-(phenylmethyl)-2h-phthalazin-1-one,2.8\nCc1[nH]c(\\C=C\\2/C(=O)Nc3ccc(F)cc23)c(C)c1C(=O)NC[C@H](O)CN4CCOCC4,\"InChI=1S/C23H27FN4O4/c1-13-20(10-18-17-9-15(24)3-4-19(17)27-22(18)30)26-14(2)21(13)23(31)25-11-16(29)12-28-5-7-32-8-6-28/h3-4,9-10,16,26,29H,5-8,11-12H2,1-2H3,(H,25,31)(H,27,30)/b18-10-/t16-/m0/s1\",[C][C][NH1][C][Branch2][Ring1][Branch1][\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][\\-Ring1][O][Ring1][#Branch1][=C][Branch1][C][C][C][=Ring2][Ring1][C][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][N][C][C][O][C][C][Ring1][=Branch1],\"5-[(z)-(5-fluoro-2-oxo-1h-indol-3-ylidene)methyl]-n-[(2s)-2-hydroxy-3-morpholin-4-ylpropyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide\",2.22\nCOc1ccc(NC(=O)CCc2c(C)nc3nc(C)nn3c2C)cc1,\"InChI=1S/C18H21N5O2/c1-11-16(12(2)23-18(19-11)20-13(3)22-23)9-10-17(24)21-14-5-7-15(25-4)8-6-14/h5-8H,9-10H2,1-4H3,(H,21,24)\",[C][O][C][=C][C][=C][Branch2][Ring1][N][N][C][=Branch1][C][=O][C][C][C][C][Branch1][C][C][=N][C][=N][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=Ring1][O][C][C][=C][Ring2][Ring1][#Branch1],\"n-(4-methoxyphenyl)-3-(2,5,7-trimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)propanamide\",1.4\nCCOC(=O)c1ccc(OCCC2CCN(CC2)c3ccc(C)nn3)cc1,\"InChI=1S/C21H27N3O3/c1-3-26-21(25)18-5-7-19(8-6-18)27-15-12-17-10-13-24(14-11-17)20-9-4-16(2)22-23-20/h4-9,17H,3,10-15H2,1-2H3\",[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][O][C][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][C][N][=N][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch1],ethyl 4-[2-[1-(6-methylpyridazin-3-yl)piperidin-4-yl]ethoxy]benzoate,4.42\nCOc1ccc(cc1C(=O)NCc2cccnc2)C(=O)NCc3cccnc3,\"InChI=1S/C21H20N4O3/c1-28-19-7-6-17(20(26)24-13-15-4-2-8-22-11-15)10-18(19)21(27)25-14-16-5-3-9-23-12-16/h2-12H,13-14H2,1H3,(H,24,26)(H,25,27)\",[C][O][C][=C][C][=C][Branch2][Ring1][Ring1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1],\"4-methoxy-n,n'-bis(pyridin-3-ylmethyl)benzene-1,3-dicarboxamide\",1.23\nCN(C)CCOc1ccc(cc1)c2cc(C(=O)N)c(NC(=O)N)s2,\"InChI=1S/C16H20N4O3S/c1-20(2)7-8-23-11-5-3-10(4-6-11)13-9-12(14(17)21)15(24-13)19-16(18)22/h3-6,9H,7-8H2,1-2H3,(H2,17,21)(H3,18,19,22)\",[C][N][Branch1][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][N][S][Ring1][N],2-(carbamoylamino)-5-[4-(2-dimethylaminoethoxy)phenyl]thiophene-3-carboxamide,1.16\nCc1ccc(cc1)c2cc(C(=O)N3CCOCC3)c4cc(C)ccc4n2,\"InChI=1S/C22H22N2O2/c1-15-3-6-17(7-4-15)21-14-19(22(25)24-9-11-26-12-10-24)18-13-16(2)5-8-20(18)23-21/h3-8,13-14H,9-12H2,1-2H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Branch1][C][C][C][=C][C][Ring1][#Branch1][=N][Ring2][Ring1][Ring1],[6-methyl-2-(4-methylphenyl)quinolin-4-yl]-morpholin-4-ylmethanone,3.6\nCCOc1ccc2C=CC(=O)Oc2c1,\"InChI=1S/C11H10O3/c1-2-13-9-5-3-8-4-6-11(12)14-10(8)7-9/h3-7H,2H2,1H3\",[C][C][O][C][=C][C][=C][C][=C][C][=Branch1][C][=O][O][C][Ring1][#Branch1][=C][Ring1][O],7-ethoxychromen-2-one,2.2\nCOc1cc2c(Nc3cnc(NC(=O)c4ccccc4)nc3)ncnc2cc1OCCCN5CCOCC5,\"InChI=1S/C27H29N7O4/c1-36-23-14-21-22(15-24(23)38-11-5-8-34-9-12-37-13-10-34)30-18-31-25(21)32-20-16-28-27(29-17-20)33-26(35)19-6-3-2-4-7-19/h2-4,6-7,14-18H,5,8-13H2,1H3,(H,30,31,32)(H,28,29,33,35)\",[C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][N][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][#C][N][=C][N][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1],n-[5-[[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-yl]amino]pyrimidin-2-yl]benzamide,2.7\nCN1C(=O)N(C)c2nc[nH]c2C1=O,\"InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)\",[C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][NH1][C][=Ring1][Branch1][C][Ring1][O][=O],\"1,3-dimethyl-7h-purine-2,6-dione\",-0.09\nCOc1cc(ccc1Cn2ccc3ccc(NC(=O)OC4CCCC4)cc23)C(=O)O,\"InChI=1S/C23H24N2O5/c1-29-21-12-16(22(26)27)6-7-17(21)14-25-11-10-15-8-9-18(13-20(15)25)24-23(28)30-19-4-2-3-5-19/h6-13,19H,2-5,14H2,1H3,(H,24,28)(H,26,27)\",[C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][O],4-[[6-(cyclopentyloxycarbonylamino)indol-1-yl]methyl]-3-methoxybenzoic acid,2.1\nBrc1cnc(Nc2cccc(NC(=O)N3CCCC3)c2)nc1NCCCNC(=O)c4cccs4,\"InChI=1S/C23H26BrN7O2S/c24-18-15-27-22(30-20(18)25-9-5-10-26-21(32)19-8-4-13-34-19)28-16-6-3-7-17(14-16)29-23(33)31-11-1-2-12-31/h3-4,6-8,13-15H,1-2,5,9-12H2,(H,26,32)(H,29,33)(H2,25,27,28,30)\",[Br][C][=C][N][=C][Branch2][Ring1][Branch2][N][C][=C][C][=C][C][Branch1][=N][N][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=C][Ring1][=C][N][=C][Ring2][Ring1][Branch1][N][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][S][Ring1][Branch1],n-[3-[[5-bromo-4-[3-(thiophene-2-carbonylamino)propylamino]pyrimidin-2-yl]amino]phenyl]pyrrolidine-1-carboxamide,4.13\nCCOc1ccc(CCNCCCSCCNC[C@H](O)c2ccc(O)c3NC(=O)Sc23)cc1,\"InChI=1S/C24H33N3O4S2/c1-2-31-18-6-4-17(5-7-18)10-12-25-11-3-14-32-15-13-26-16-21(29)19-8-9-20(28)22-23(19)33-24(30)27-22/h4-9,21,25-26,28-29H,2-3,10-16H2,1H3,(H,27,30)/t21-/m0/s1\",[C][C][O][C][=C][C][=C][Branch2][Ring2][Ring1][C][C][N][C][C][C][S][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1][C][=C][Ring2][Ring1][=C],\"7-[(1r)-2-[2-[3-[2-(4-ethoxyphenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",0.41\nOC(=O)CCc1oc(c2ccccc2)c(n1)c3ccccc3,\"InChI=1S/C18H15NO3/c20-16(21)12-11-15-19-17(13-7-3-1-4-8-13)18(22-15)14-9-5-2-6-10-14/h1-10H,11-12H2,(H,20,21)\",[O][C][=Branch1][C][=O][C][C][C][O][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Branch1][Ring2][N][=Ring1][O][C][C][=C][C][=C][C][=Ring1][=Branch1],\"3-[4,5-di(phenyl)-1,3-oxazol-2-yl]propanoic acid\",1.2\nCC(C)OC(=O)N1CCC(CC1)Oc2ncnc3c2cnn3c4ccc(cc4F)S(=O)(=O)C,\"InChI=1S/C21H24FN5O5S/c1-13(2)31-21(28)26-8-6-14(7-9-26)32-20-16-11-25-27(19(16)23-12-24-20)18-5-4-15(10-17(18)22)33(3,29)30/h4-5,10-14H,6-9H2,1-3H3\",[C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][=C][Ring1][=Branch1][C][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C],\"propan-2-yl 4-[1-(2-fluoro-4-methylsulfonylphenyl)pyrazolo[4,5-e]pyrimidin-4-yl]oxypiperidine-1-carboxylate\",3\nCOc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN(C)[C@H](C)C(=O)N,\"InChI=1S/C20H21ClFN5O2/c1-11(19(23)28)27(2)9-12-7-13-16(8-17(12)29-3)24-10-25-20(13)26-15-6-4-5-14(21)18(15)22/h4-8,10-11H,9H2,1-3H3,(H2,23,28)(H,24,25,26)/t11-/m1/s1\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][Branch1][C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][N],(2r)-2-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl-methylamino]propanamide,3.44\nN(c1cccnc1)c2ncnc3ccccc23,\"InChI=1S/C13H10N4/c1-2-6-12-11(5-1)13(16-9-15-12)17-10-4-3-7-14-8-10/h1-9H,(H,15,16,17)\",[N][Branch1][=Branch2][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],n-pyridin-3-ylquinazolin-4-amine,1.57\nCOCCOc1ccc(cc1)C(=O)Nc2cc(NC(=O)c3cccc(c3)N(C)C)ccc2C,\"InChI=1S/C26H29N3O4/c1-18-8-11-21(27-26(31)20-6-5-7-22(16-20)29(2)3)17-24(18)28-25(30)19-9-12-23(13-10-19)33-15-14-32-4/h5-13,16-17H,14-15H2,1-4H3,(H,27,31)(H,28,30)\",[C][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][C][C],3-dimethylamino-n-[3-[[4-(2-methoxyethoxy)benzoyl]amino]-4-methylphenyl]benzamide,2.74\nCC(C)Cn1cnc2c(N)nc3ccccc3c12,\"InChI=1S/C14H16N4/c1-9(2)7-18-8-16-12-13(18)10-5-3-4-6-11(10)17-14(12)15/h3-6,8-9H,7H2,1-2H3,(H2,15,17)\",[C][C][Branch1][C][C][C][N][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][=C][Ring1][O],\"1-(2-methylpropyl)imidazo[4,5-c]quinolin-4-amine\",2.52\nC[S+]([O-])c1ccc(\\C=C/2\\C(=C(CC(=O)O)c3cc(F)ccc23)C)cc1,\"InChI=1S/C20H17FO3S/c1-12-17(9-13-3-6-15(7-4-13)25(2)24)16-8-5-14(21)10-19(16)18(12)11-20(22)23/h3-10H,11H2,1-2H3,(H,22,23)/b17-9-\",[C][S+1][Branch1][C][O-1][C][=C][C][=C][Branch2][Ring1][=C][\\C][=C][\\C][=Branch2][Ring1][#Branch1][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][F][=C][C][=C][/-Ring1][=C][Ring1][#Branch1][C][C][=C][Ring2][Ring1][=Branch1],2-[(3z)-6-fluoro-2-methyl-3-[(4-methylsulfinylphenyl)methylidene]inden-1-yl]acetic acid,-0.01\nCc1oc(nc1CCOc2ccc(C[C@H](Nc3ccccc3C(=O)c4ccccc4)C(=O)O)cc2)c5ccccc5,\"InChI=1S/C34H30N2O5/c1-23-29(36-33(41-23)26-12-6-3-7-13-26)20-21-40-27-18-16-24(17-19-27)22-31(34(38)39)35-30-15-9-8-14-28(30)32(37)25-10-4-2-5-11-25/h2-19,31,35H,20-22H2,1H3,(H,38,39)/t31-/m0/s1\",[C][C][O][C][=Branch2][Branch1][Ring1][=N][C][=Ring1][Branch1][C][C][O][C][=C][C][=C][Branch2][Ring1][S][C][C@H1][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],\"(2s)-2-[[2-(benzoyl)phenyl]amino]-3-[4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]phenyl]propanoic acid\",3.5\nCN(C)CCCN1c2ccccc2Sc3ccc(cc13)C(F)(F)F,\"InChI=1S/C18H19F3N2S/c1-22(2)10-5-11-23-14-6-3-4-7-16(14)24-17-9-8-13(12-15(17)23)18(19,20)21/h3-4,6-9,12H,5,10-11H2,1-2H3\",[C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"n,n-dimethyl-3-[2-(trifluoromethyl)phenothiazin-10-yl]propan-1-amine\",3.59\nCN(C)c1ccnc2sc(C(=O)N)c(N)c12,\"InChI=1S/C10H12N4OS/c1-14(2)5-3-4-13-10-6(5)7(11)8(16-10)9(12)15/h3-4H,11H2,1-2H3,(H2,12,15)\",[C][N][Branch1][C][C][C][=C][C][=N][C][S][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][C][N][C][Ring1][=N][=Ring1][=Branch2],\"3-amino-4-dimethylaminothieno[5,4-b]pyridine-2-carboxamide\",1.7\nCOc1ccc(cc1)C(CN(C)C)C2(O)CCCCC2,\"InChI=1S/C17H27NO2/c1-18(2)13-16(17(19)11-5-4-6-12-17)14-7-9-15(20-3)10-8-14/h7-10,16,19H,4-6,11-13H2,1-3H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][#Branch1][C][N][Branch1][C][C][C][C][Branch1][C][O][C][C][C][C][C][Ring1][#Branch1],1-[2-dimethylamino-1-(4-methoxyphenyl)ethyl]cyclohexan-1-ol,0.99\nCc1cc(CN2CCC2)cnc1c3ccc(cc3)C(=O)Nc4ccccc4N,\"InChI=1S/C23H24N4O/c1-16-13-17(15-27-11-4-12-27)14-25-22(16)18-7-9-19(10-8-18)23(28)26-21-6-3-2-5-20(21)24/h2-3,5-10,13-14H,4,11-12,15,24H2,1H3,(H,26,28)\",[C][C][=C][C][Branch1][Branch2][C][N][C][C][C][Ring1][Ring2][=C][N][=C][Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N],n-(2-aminophenyl)-4-[5-(azetidin-1-ylmethyl)-3-methylpyridin-2-yl]benzamide,1.18\nNC(=O)C([C@@H]1CCN(CCc2ccc3OCCc3c2)C1)(c4ccccc4)c5ccccc5,\"InChI=1S/C28H30N2O2/c29-27(31)28(23-7-3-1-4-8-23,24-9-5-2-6-10-24)25-14-17-30(20-25)16-13-21-11-12-26-22(19-21)15-18-32-26/h1-12,19,25H,13-18,20H2,(H2,29,31)/t25-/m1/s1\",[N][C][=Branch1][C][=O][C][Branch2][Ring1][=Branch2][C@@H1][C][C][N][Branch1][S][C][C][C][=C][C][=C][O][C][C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][Ring1][S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[(3s)-1-[2-(2,3-dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-di(phenyl)acetamide\",2.79\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4cc(ccc34)C(F)(F)F,\"InChI=1S/C22H17F3N2O2/c1-12-3-6-19-17(9-12)21(13(2)27(19)11-20(28)29)16-7-8-26-18-10-14(22(23,24)25)4-5-15(16)18/h3-10H,11H2,1-2H3,(H,28,29)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"2-[2,5-dimethyl-3-[7-(trifluoromethyl)quinolin-4-yl]indol-1-yl]acetic acid\",1.78\nCN(C)CCN(Cc1ccccc1)c2ccccn2,\"InChI=1S/C16H21N3/c1-18(2)12-13-19(16-10-6-7-11-17-16)14-15-8-4-3-5-9-15/h3-11H,12-14H2,1-2H3\",[C][N][Branch1][C][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1],\"n',n'-dimethyl-n-(phenylmethyl)-n-pyridin-2-ylethane-1,2-diamine\",1.28\nCC(CCc1ccccc1)NCC(O)c2ccc(O)c(c2)C(=O)N,\"InChI=1S/C19H24N2O3/c1-13(7-8-14-5-3-2-4-6-14)21-12-18(23)15-9-10-17(22)16(11-15)19(20)24/h2-6,9-11,13,18,21-23H,7-8,12H2,1H3,(H2,20,24)\",[C][C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N],2-hydroxy-5-[1-hydroxy-2-(4-phenylbutan-2-ylamino)ethyl]benzamide,1.06\nCCN(CC)CCNC(=O)c1cc(Cl)c(N)cc1OC,\"InChI=1S/C14H22ClN3O2/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3/h8-9H,4-7,16H2,1-3H3,(H,17,19)\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][N][C][=C][Ring1][Branch2][O][C],4-amino-5-chloro-n-(2-diethylaminoethyl)-2-methoxybenzamide,0.34\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3ccccn3)C(=O)C(F)(F)F,\"InChI=1S/C26H26F3N5O4/c1-16(2)22(23(36)26(27,28)29)33-21(35)15-34-20(17-8-4-3-5-9-17)12-11-19(24(34)37)32-25(38)31-14-18-10-6-7-13-30-18/h3-13,16,22H,14-15H2,1-2H3,(H,33,35)(H2,31,32,38)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[2-oxo-6-phenyl-3-(pyridin-2-ylmethylcarbamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.15\nOC(=O)Cc1ccccc1Nc2c(Cl)cccc2Cl,\"InChI=1S/C14H11Cl2NO2/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19/h1-7,17H,8H2,(H,18,19)\",[O][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl],\"2-[2-[(2,6-dichlorophenyl)amino]phenyl]acetic acid\",1.08\nNC(=O)C1=CN(Cc2ccc(Cl)cc2Cl)C(=O)C=C1,\"InChI=1S/C13H10Cl2N2O2/c14-10-3-1-8(11(15)5-10)6-17-7-9(13(16)19)2-4-12(17)18/h1-5,7H,6H2,(H2,16,19)\",[N][C][=Branch1][C][=O][C][=C][N][Branch1][=C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][C][=Branch1][C][=O][C][=C][Ring1][S],\"1-[(2,4-dichlorophenyl)methyl]-6-oxopyridine-3-carboxamide\",2.36\nCCc1cc(ccn1)C(=S)N,\"InChI=1S/C8H10N2S/c1-2-7-5-6(8(9)11)3-4-10-7/h3-5H,2H2,1H3,(H2,9,11)\",[C][C][C][=C][C][=Branch1][=Branch1][=C][C][=N][Ring1][=Branch1][C][=Branch1][C][=S][N],2-ethylpyridine-4-carbothioamide,1.52\nCOc1cccc(NC(=O)c2cccc(Cc3c(C)nn(CCO)c3c4ccccc4)c2)c1,\"InChI=1S/C27H27N3O3/c1-19-25(26(30(29-19)14-15-31)21-9-4-3-5-10-21)17-20-8-6-11-22(16-20)27(32)28-23-12-7-13-24(18-23)33-2/h3-13,16,18,31H,14-15,17H2,1-2H3,(H,28,32)\",[C][O][C][=C][C][=C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring1][=Branch2][C][C][C][Branch1][C][C][=N][N][Branch1][Ring2][C][C][O][C][=Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring2][Ring1][=Branch1][=C][Ring2][Ring1][#C],3-[[1-(2-hydroxyethyl)-3-methyl-5-phenylpyrazol-4-yl]methyl]-n-(3-methoxyphenyl)benzamide,4.29\nCOc1ccc(CC(=O)Nc2nc3ccccc3[nH]2)cc1,\"InChI=1S/C16H15N3O2/c1-21-12-8-6-11(7-9-12)10-15(20)19-16-17-13-4-2-3-5-14(13)18-16/h2-9H,10H2,1H3,(H2,17,18,19,20)\",[C][O][C][=C][C][=C][Branch2][Ring1][Ring2][C][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=C][Ring2][Ring1][Ring1],n-(1h-benzimidazol-2-yl)-2-(4-methoxyphenyl)acetamide,2.9\nCOc1cc(OC)cc(c1)c2cc3cnc(N)nc3nc2N,\"InChI=1S/C15H15N5O2/c1-21-10-3-8(4-11(6-10)22-2)12-5-9-7-18-15(17)20-14(9)19-13(12)16/h3-7H,1-2H3,(H4,16,17,18,19,20)\",[C][O][C][=C][C][Branch1][Ring1][O][C][=C][C][=Branch1][Ring2][=C][Ring1][Branch2][C][=C][C][=C][N][=C][Branch1][C][N][N][=C][Ring1][#Branch1][N][=C][Ring1][O][N],\"6-(3,5-dimethoxyphenyl)pyrido[6,5-d]pyrimidine-2,7-diamine\",2.14\nCOc1ccc(cc1CO)c2ccc3c(nc(nc3n2)N4C[C@@H](C)O[C@@H](C)C4)N5CCOCC5,\"InChI=1S/C25H31N5O4/c1-16-13-30(14-17(2)34-16)25-27-23-20(24(28-25)29-8-10-33-11-9-29)5-6-21(26-23)18-4-7-22(32-3)19(12-18)15-31/h4-7,12,16-17,31H,8-11,13-15H2,1-3H3/t16-,17+\",[C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][C][O][C][=C][C][=C][C][=Branch2][Ring1][#Branch2][=N][C][=Branch1][Branch2][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2][N][C][C@@H1][Branch1][C][C][O][C@@H1][Branch1][C][C][C][Ring1][Branch2][N][C][C][O][C][C][Ring1][=Branch1],\"[5-[2-[(2r,6s)-2,6-dimethylmorpholin-4-yl]-4-morpholin-4-ylpyrido[5,6-e]pyrimidin-7-yl]-2-methoxyphenyl]methanol\",3.25\nCc1c(Sc2ccc(Cl)cc2)c3ccc(Cl)cc3n1CC(=O)O,\"InChI=1S/C17H13Cl2NO2S/c1-10-17(23-13-5-2-11(18)3-6-13)14-7-4-12(19)8-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],2-[6-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid,2.51\nCNC(=O)c1ccc(Nc2nccc(n2)c3cnc(C)n3C(C)C)cc1F,\"InChI=1S/C19H21FN6O/c1-11(2)26-12(3)23-10-17(26)16-7-8-22-19(25-16)24-13-5-6-14(15(20)9-13)18(27)21-4/h5-11H,1-4H3,(H,21,27)(H,22,24,25)\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][=Branch1][F],2-fluoro-n-methyl-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide,2.95\nCC12CCC3C(CCC4=CC(=O)CCC34C)C1CCC2O,\"InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3\",[C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O],\"17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one\",3.3\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CCCC4,\"InChI=1S/C24H26F3N3O3S/c1-14(2)13-30-22-19(20(31)28(3)23(30)33)18(21(32)29-10-6-7-11-29)17(34-22)12-15-8-4-5-9-16(15)24(25,26)27/h4-5,8-9,14H,6-7,10-13H2,1-3H3\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1],\"3-methyl-1-(2-methylpropyl)-5-(pyrrolidine-1-carbonyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\",3.8\nO=C1N2CCS(=O)(=O)C2=Nc3ccccc13,\"InChI=1S/C10H8N2O3S/c13-9-7-3-1-2-4-8(7)11-10-12(9)5-6-16(10,14)15/h1-4H,5-6H2\",[O][=C][N][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][Ring1][#Branch1][=N][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"1,1-dioxo-2,3-dihydro-[1,3]thiazolo[2,3-b]quinazolin-5-one\",0.8\nCCOC(=O)c1c(C)n(Cc2occc2)c3ccc(O)cc13,\"InChI=1S/C17H17NO4/c1-3-21-17(20)16-11(2)18(10-13-5-4-8-22-13)15-7-6-12(19)9-14(15)16/h4-9,19H,3,10H2,1-2H3\",[C][C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][Branch1][=Branch2][C][C][O][C][=C][C][=Ring1][Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][P][Ring1][#Branch1],ethyl 1-(furan-2-ylmethyl)-5-hydroxy-2-methylindole-3-carboxylate,3.5\nCOCc1c(nc(C(C)C)c(\\C=C\\[C@@H](O)C[C@@H](O)CC(=O)O)c1c2ccc(F)cc2)C(C)C,\"InChI=1S/C26H34FNO5/c1-15(2)25-21(11-10-19(29)12-20(30)13-23(31)32)24(17-6-8-18(27)9-7-17)22(14-33-5)26(28-25)16(3)4/h6-11,15-16,19-20,29-30H,12-14H2,1-5H3,(H,31,32)/b11-10+/t19-,20-/m1/s1\",[C][O][C][C][=C][Branch2][Ring2][=C][N][=C][Branch1][=Branch1][C][Branch1][C][C][C][C][Branch2][Ring1][C][\\C][=C][\\C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][=C][Ring2][Ring1][Ring2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Branch1][C][C][C],\"(e,3r,5s)-7-[4-(4-fluorophenyl)-5-(methoxymethyl)-2,6-di(propan-2-yl)pyridin-3-yl]-3,5-dihydroxyhept-6-enoic acid\",1.72\n[O-][N+](=O)c1ccc2C(=O)C(=O)c3ccccc3c2c1,InChI=1S/C14H7NO4/c16-13-10-4-2-1-3-9(10)12-7-8(15(18)19)5-6-11(12)14(13)17/h1-7H,[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S],\"3-nitrophenanthrene-9,10-dione\",2.56\nCC12CC3CC(C)(C1)CC(N)(C3)C2,\"InChI=1S/C12H21N/c1-10-3-9-4-11(2,6-10)8-12(13,5-9)7-10/h9H,3-8,13H2,1-2H3\",[C][C][C][C][C][C][Branch1][C][C][Branch1][Ring2][C][Ring1][#Branch1][C][C][Branch1][C][N][Branch1][Ring2][C][Ring1][=Branch2][C][Ring1][N],\"3,5-dimethyladamantan-1-amine\",0.06\nCc1cc(Nc2ccc(F)cc2)nc(N)n1,\"InChI=1S/C11H11FN4/c1-7-6-10(16-11(13)14-7)15-9-4-2-8(12)3-5-9/h2-6H,1H3,(H3,13,14,15,16)\",[C][C][=C][C][Branch1][=N][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][=N][C][Branch1][C][N][=N][Ring1][#C],\"n'-(4-fluorophenyl)-6-methylpyrimidine-2,4-diamine\",2.08\nCC(=O)Nc1ccccn1,\"InChI=1S/C7H8N2O/c1-6(10)9-7-4-2-3-5-8-7/h2-5H,1H3,(H,8,9,10)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1],n-pyridin-2-ylacetamide,0.5\nCCOC(=O)c1ccccc1c2csc(NS(=O)(=O)c3ccc(Cl)cc3)n2,\"InChI=1S/C18H15ClN2O4S2/c1-2-25-17(22)15-6-4-3-5-14(15)16-11-26-18(20-16)21-27(23,24)13-9-7-12(19)8-10-13/h3-11H,2H2,1H3,(H,20,21)\",[C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][S][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][S],\"ethyl 2-[2-[(4-chlorophenyl)sulfonylamino]-1,3-thiazol-4-yl]benzoate\",2.43\nOc1ccc(cc1)N2C(=O)c3ccccc3C2=O,\"InChI=1S/C14H9NO3/c16-10-7-5-9(6-8-10)15-13(17)11-3-1-2-4-12(11)14(15)18/h1-8,16H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O],\"2-(4-hydroxyphenyl)isoindole-1,3-dione\",2\nCn1cc(cc1C=O)C(=O)CCCCOc2ccc(cc2)C(=O)O,\"InChI=1S/C18H19NO5/c1-19-11-14(10-15(19)12-20)17(21)4-2-3-9-24-16-7-5-13(6-8-16)18(22)23/h5-8,10-12H,2-4,9H2,1H3,(H,22,23)\",[C][N][C][=C][Branch1][#Branch1][C][=C][Ring1][Branch1][C][=O][C][=Branch1][C][=O][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O],4-[5-(5-formyl-1-methylpyrrol-3-yl)-5-oxopentoxy]benzoic acid,0.14\nNc1ccccc1NC(=O)c2ccc(CNC(=O)OCc3cccnc3)cc2,\"InChI=1S/C21H20N4O3/c22-18-5-1-2-6-19(18)25-20(26)17-9-7-15(8-10-17)13-24-21(27)28-14-16-4-3-11-23-12-16/h1-12H,13-14,22H2,(H,24,27)(H,25,26)\",[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][P][C][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][C],pyridin-3-ylmethyl n-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate,1.26\nCc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(C)c4Cl,\"InChI=1S/C25H31Cl2N3O4S/c1-17-3-5-21(6-4-17)35(32,33)28-25(31)30-13-9-19(10-14-30)29-15-11-20(12-16-29)34-23-8-7-22(26)18(2)24(23)27/h3-8,19-20H,9-16H2,1-2H3,(H,28,31)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][C][=C][Ring1][Branch2][Cl],\"4-[4-(2,4-dichloro-3-methylphenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\",2.2\nCOc1ccc(cc1OC)C(=O)Nc2cccc(NC(=O)c3ccc(OC)c(OC)c3)n2,\"InChI=1S/C23H23N3O6/c1-29-16-10-8-14(12-18(16)31-3)22(27)25-20-6-5-7-21(24-20)26-23(28)15-9-11-17(30-2)19(13-15)32-4/h5-13H,1-4H3,(H2,24,25,26,27,28)\",[C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][=N][Ring2][Ring1][Ring1],\"n-[6-[(3,4-dimethoxybenzoyl)amino]pyridin-2-yl]-3,4-dimethoxybenzamide\",3.5\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCN4CCCC4,\"InChI=1S/C21H22ClFN4O2/c1-28-19-12-18-15(11-20(19)29-9-8-27-6-2-3-7-27)21(25-13-24-18)26-14-4-5-17(23)16(22)10-14/h4-5,10-13H,2-3,6-9H2,1H3,(H,24,25,26)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][C][C][C][C][Ring1][Branch1],n-(3-chloro-4-fluorophenyl)-7-methoxy-6-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine,3.28\nCC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(c(F)c2)n3ccnc3,\"InChI=1S/C15H15FN4O3/c1-10(21)18-7-12-8-20(15(22)23-12)11-2-3-14(13(16)6-11)19-5-4-17-9-19/h2-6,9,12H,7-8H2,1H3,(H,18,21)/t12-/m0/s1\",[C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][F][=C][Ring1][#Branch1][N][C][=C][N][=C][Ring1][Branch1],\"n-[[(5s)-3-(3-fluoro-4-imidazol-1-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\",0.7\nCN1SC(=O)c2cc(ccc12)S(=O)(=O)N,\"InChI=1S/C8H8N2O3S2/c1-10-7-3-2-5(15(9,12)13)4-6(7)8(11)14-10/h2-4H,1H3,(H2,9,12,13)\",[C][N][S][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N],\"1-methyl-3-oxo-2,1-benzothiazole-5-sulfonamide\",0.3\nOC1CCN(CC1)C(=O)CN2C(=O)C(Cc3ccccc23)NC(=O)c4cc5cc(Cl)sc5[nH]4,\"InChI=1S/C23H23ClN4O4S/c24-19-11-14-10-16(26-22(14)33-19)21(31)25-17-9-13-3-1-2-4-18(13)28(23(17)32)12-20(30)27-7-5-15(29)6-8-27/h1-4,10-11,15,17,26,29H,5-9,12H2,(H,25,31)\",[O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-[2-(4-hydroxypiperidin-1-yl)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",2.86\nC(Cc1nc2ccccc2[nH]1)Cc3nc4ccccc4[nH]3,\"InChI=1S/C17H16N4/c1-2-7-13-12(6-1)18-16(19-13)10-5-11-17-20-14-8-3-4-9-15(14)21-17/h1-4,6-9H,5,10-11H2,(H,18,19)(H,20,21)\",[C][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],2-[3-(1h-benzimidazol-2-yl)propyl]-1h-benzimidazole,3.5\nCc1ccc2c(c1)c(Sc3ccccc3Cl)c(C)n2CC(=O)O,\"InChI=1S/C18H16ClNO2S/c1-11-7-8-15-13(9-11)18(12(2)20(15)10-17(21)22)23-16-6-4-3-5-14(16)19/h3-9H,10H2,1-2H3,(H,21,22)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][O][S][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O],\"2-[3-(2-chlorophenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\",1.71\nCOc1ccc(C[C@@H](C)NC[C@H](O)c2ccc(O)c(NC=O)c2)cc1,\"InChI=1S/C19H24N2O4/c1-13(9-14-3-6-16(25-2)7-4-14)20-11-19(24)15-5-8-18(23)17(10-15)21-12-22/h3-8,10,12-13,19-20,23-24H,9,11H2,1-2H3,(H,21,22)/t13-,19+/m1/s1\",[C][O][C][=C][C][=C][Branch2][Ring1][N][C][C@@H1][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][Branch1][Ring2][N][C][=O][=C][Ring1][#Branch2][C][=C][Ring2][Ring1][#Branch1],n-[2-hydroxy-5-[(1r)-1-hydroxy-2-[[(2r)-1-(4-methoxyphenyl)propan-2-yl]amino]ethyl]phenyl]formamide,0.42\nOC[C@H](O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)ccc4[nH]3,\"InChI=1S/C21H20ClN3O4/c22-14-5-6-16-13(7-14)9-17(23-16)20(28)24-18-8-12-3-1-2-4-19(12)25(21(18)29)10-15(27)11-26/h1-7,9,15,18,23,26-27H,8,10-11H2,(H,24,28)/t15-,18?/m1/s1\",[O][C][C@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],\"5-chloro-n-[1-[(2r)-2,3-dihydroxypropyl]-2-oxo-3,4-dihydroquinolin-3-yl]-1h-indole-2-carboxamide\",3.4\nCC(=O)C1=C(C)c2cnc(Nc3ccc(cn3)N4CCNCC4)nc2N(C5CCCC5)C1=O,\"InChI=1S/C24H29N7O2/c1-15-19-14-27-24(28-20-8-7-18(13-26-20)30-11-9-25-10-12-30)29-22(19)31(17-5-3-4-6-17)23(33)21(15)16(2)32/h7-8,13-14,17,25H,3-6,9-12H2,1-2H3,(H,26,27,28,29)\",[C][C][=Branch1][C][=O][C][=C][Branch1][C][C][C][=C][N][=C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][N][C][C][N][C][C][Ring1][=Branch1][N][=C][Ring2][Ring1][Ring1][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][Ring2][Ring1][=N][=O],\"6-acetyl-8-cyclopentyl-5-methyl-2-[(5-piperazin-1-ylpyridin-2-yl)amino]pyrido[6,5-d]pyrimidin-7-one\",0.8\nCC(=O)N1CCN(CC1)c2ccc(NC(=O)c3oc(Nc4ccccc4F)nn3)cc2,\"InChI=1S/C21H21FN6O3/c1-14(29)27-10-12-28(13-11-27)16-8-6-15(7-9-16)23-19(30)20-25-26-21(31-20)24-18-5-3-2-4-17(18)22/h2-9H,10-13H2,1H3,(H,23,30)(H,24,26)\",[C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][O][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][N][=Ring1][=N][C][=C][Ring2][Ring1][=Branch1],\"n-[4-(4-acetylpiperazin-1-yl)phenyl]-5-[(2-fluorophenyl)amino]-1,3,4-oxadiazole-2-carboxamide\",2.51\nCC1=C(C(=O)N(C[C@H](N)c2ccccc2)C(=O)N1Cc3c(F)cccc3F)c4ccccc4F,\"InChI=1S/C26H22F3N3O2/c1-16-24(18-10-5-6-11-20(18)27)25(33)32(15-23(30)17-8-3-2-4-9-17)26(34)31(16)14-19-21(28)12-7-13-22(19)29/h2-13,23H,14-15,30H2,1H3/t23-/m0/s1\",[C][C][=C][Branch2][Ring2][=Branch2][C][=Branch1][C][=O][N][Branch1][=C][C][C@H1][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][P][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F],\"3-[(2r)-2-amino-2-phenylethyl]-1-[(2,6-difluorophenyl)methyl]-5-(2-fluorophenyl)-6-methylpyrimidine-2,4-dione\",2.76\nOS(=N)(=O)Cc1noc2ccccc12,\"InChI=1S/C8H8N2O3S/c9-14(11,12)5-7-6-3-1-2-4-8(6)13-10-7/h1-4H,5H2,(H2,9,11,12)\",[O][S][=Branch1][C][=N][=Branch1][C][=O][C][C][=N][O][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1],\"1,2-benzoxazol-3-ylmethanesulfonimidic acid\",0.55\nClc1ccc2[nH]ccc2c1,\"InChI=1S/C8H6ClN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H\",[Cl][C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2],5-chloro-1h-indole,3.28\nCN(C)C(=O)[C@H](Cc1ccccc1)NC(=O)c2cc3cc(F)ccc3[nH]2,\"InChI=1S/C20H20FN3O2/c1-24(2)20(26)18(10-13-6-4-3-5-7-13)23-19(25)17-12-14-11-15(21)8-9-16(14)22-17/h3-9,11-12,18,22H,10H2,1-2H3,(H,23,25)/t18-/m0/s1\",[C][N][Branch1][C][C][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],n-[(2s)-1-dimethylamino-1-oxo-3-phenylpropan-2-yl]-5-fluoro-1h-indole-2-carboxamide,3.5\nCOc1cc(NC(=O)Nc2cccc(CNC(=O)O[C@H]3CCOC3)c2)ccc1c4ocnc4,\"InChI=1S/C23H24N4O6/c1-30-20-10-17(5-6-19(20)21-12-24-14-32-21)27-22(28)26-16-4-2-3-15(9-16)11-25-23(29)33-18-7-8-31-13-18/h2-6,9-10,12,14,18H,7-8,11,13H2,1H3,(H,25,29)(H2,26,27,28)/t18-/m0/s1\",[C][O][C][=C][C][Branch2][Ring1][#C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][#C][C][N][C][=Branch1][C][=O][O][C@H1][C][C][O][C][Ring1][Branch1][=C][Ring1][S][=C][C][=C][Ring2][Ring1][#Branch2][C][O][C][=N][C][=Ring1][Branch1],\"[(3s)-oxolan-3-yl] n-[[3-[[3-methoxy-4-(1,3-oxazol-5-yl)phenyl]carbamoylamino]phenyl]methyl]carbamate\",3.6\nClc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C23H26Cl3N3O4S/c24-16-1-4-20(5-2-16)34(31,32)27-23(30)29-11-7-17(8-12-29)28-13-9-18(10-14-28)33-19-3-6-21(25)22(26)15-19/h1-6,15,17-18H,7-14H2,(H,27,30)\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"n-(4-chlorophenyl)sulfonyl-4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidine-1-carboxamide\",2.59\nCN1C(=O)NC(=O)C(C)(C2=CCCCC2)C1=O,\"InChI=1S/C12H16N2O3/c1-12(8-6-4-3-5-7-8)9(15)13-11(17)14(2)10(12)16/h6H,3-5,7H2,1-2H3,(H,13,15,17)\",[C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][=Branch2][C][=C][C][C][C][C][Ring1][=Branch1][C][Ring1][#C][=O],\"5-(1-cyclohexenyl)-1,5-dimethyl-1,3-diazinane-2,4,6-trione\",1.5\nClc1ccc2N(C3CCN(CCCN4C(=O)Nc5ccccc45)CC3)C(=O)Nc2c1,\"InChI=1S/C22H24ClN5O2/c23-15-6-7-20-18(14-15)25-22(30)28(20)16-8-12-26(13-9-16)10-3-11-27-19-5-2-1-4-17(19)24-21(27)29/h1-2,4-7,14,16H,3,8-13H2,(H,24,29)(H,25,30)\",[Cl][C][=C][C][=C][N][Branch2][Ring1][S][C][C][C][N][Branch2][Ring1][Ring2][C][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][N][C][Ring2][Ring1][=Branch2][=C][Ring2][Ring1][=N],6-chloro-3-[1-[3-(2-oxo-3h-benzimidazol-1-yl)propyl]piperidin-4-yl]-1h-benzimidazol-2-one,3.45\nCC1=C(C(=O)Oc2cc(O)ccc12)c3ccc(O)cc3,\"InChI=1S/C16H12O4/c1-9-13-7-6-12(18)8-14(13)20-16(19)15(9)10-2-4-11(17)5-3-10/h2-8,17-18H,1H3\",[C][C][=C][Branch2][Ring1][Ring1][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][N][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1],7-hydroxy-3-(4-hydroxyphenyl)-4-methylchromen-2-one,2.8\nCCN1C=C(C(=O)O)C(=O)c2cc(F)c(cc12)N3CCNCC3,\"InChI=1S/C16H18FN3O3/c1-2-19-9-11(16(22)23)15(21)10-7-12(17)14(8-13(10)19)20-5-3-18-4-6-20/h7-9,18H,2-6H2,1H3,(H,22,23)\",[C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][Branch1][#Branch1][C][=C][Ring1][#C][Ring1][#Branch1][N][C][C][N][C][C][Ring1][=Branch1],1-ethyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid,-0.87\nCOC(=O)c1c(O)cccc1OC\\C=C\\c2ccc(F)c(c2)c3onc(c3)C(=O)O,\"InChI=1S/C21H16FNO7/c1-28-21(27)19-16(24)5-2-6-17(19)29-9-3-4-12-7-8-14(22)13(10-12)18-11-15(20(25)26)23-30-18/h2-8,10-11,24H,9H2,1H3,(H,25,26)/b4-3+\",[C][O][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][C][=C][Ring1][#Branch1][O][C][\\C][=C][\\C][=C][C][=C][Branch1][C][F][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][N][=C][Branch1][Ring2][C][=Ring1][Branch1][C][=Branch1][C][=O][O],\"5-[2-fluoro-5-[(e)-3-(3-hydroxy-2-methoxycarbonylphenoxy)prop-1-enyl]phenyl]-1,2-oxazole-3-carboxylic acid\",0.66\nNc1nccc(n1)c2c[nH]c3ccccc23,\"InChI=1S/C12H10N4/c13-12-14-6-5-11(16-12)9-7-15-10-4-2-1-3-8(9)10/h1-7,15H,(H2,13,14,16)\",[N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1],4-(1h-indol-3-yl)pyrimidin-2-amine,1.68\nFc1ccc(cc1)c2ncn(C3CCNCC3)c2c4ccncc4,\"InChI=1S/C19H19FN4/c20-16-3-1-14(2-4-16)18-19(15-5-9-21-10-6-15)24(13-23-18)17-7-11-22-12-8-17/h1-6,9-10,13,17,22H,7-8,11-12H2\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=C][N][Branch1][=Branch2][C][C][C][N][C][C][Ring1][=Branch1][C][=Ring1][O][C][=C][C][=N][C][=C][Ring1][=Branch1],4-[5-(4-fluorophenyl)-3-piperidin-4-ylimidazol-4-yl]pyridine,0.3\nCc1cc(nc(n1)n2ccnc2)N3CCC[C@@H]3C(=O)NCCc4ccc5OCOc5c4,\"InChI=1S/C22H24N6O3/c1-15-11-20(26-22(25-15)27-10-8-23-13-27)28-9-2-3-17(28)21(29)24-7-6-16-4-5-18-19(12-16)31-14-30-18/h4-5,8,10-13,17H,2-3,6-7,9,14H2,1H3,(H,24,29)/t17-/m1/s1\",[C][C][=C][C][=Branch1][#C][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1][N][C][C][C][C@@H1][Ring1][Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2],\"(2r)-n-[2-(1,3-benzodioxol-5-yl)ethyl]-1-(2-imidazol-1-yl-6-methylpyrimidin-4-yl)pyrrolidine-2-carboxamide\",2.5\nCC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)C(=O)N(C)C)n2,\"InChI=1S/C20H24N6O/c1-13(2)26-14(3)22-12-18(26)17-10-11-21-20(24-17)23-16-8-6-15(7-9-16)19(27)25(4)5/h6-13H,1-5H3,(H,21,23,24)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][C][C][C][=N][Ring2][Ring1][C],\"n,n-dimethyl-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide\",2.45\nC=CCCCCCCCCC(=O)N[C@H]1CCC(=O)NC1=O,\"InChI=1S/C16H26N2O3/c1-2-3-4-5-6-7-8-9-10-14(19)17-13-11-12-15(20)18-16(13)21/h2,13H,1,3-12H2,(H,17,19)(H,18,20,21)/t13-/m0/s1\",[C][=C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O],\"n-[(3s)-2,6-dioxopiperidin-3-yl]undec-10-enamide\",2.64\nClc1ccc(cc1)C(=O)CN2C3=NCCN3c4ccccc24,\"InChI=1S/C17H14ClN3O/c18-13-7-5-12(6-8-13)16(22)11-21-15-4-2-1-3-14(15)20-10-9-19-17(20)21/h1-8H,9-11H2\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][N][C][=N][C][C][N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][N][Ring1][=Branch1],\"1-(4-chlorophenyl)-2-(1,2-dihydroimidazo[2,1-b]benzimidazol-4-yl)ethanone\",2.62\nCOc1cc(C)c(c(C)c1)S(=O)(=O)N(C)CCOCC(=O)N2CCC(CC2)C3CCN(C)CC3,\"InChI=1S/C25H41N3O5S/c1-19-16-23(32-5)17-20(2)25(19)34(30,31)27(4)14-15-33-18-24(29)28-12-8-22(9-13-28)21-6-10-26(3)11-7-21/h16-17,21-22H,6-15,18H2,1-5H3\",[C][O][C][=C][C][Branch1][C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][Branch1][C][C][C][C][O][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],\"4-methoxy-n,2,6-trimethyl-n-[2-[2-[4-(1-methylpiperidin-4-yl)piperidin-1-yl]-2-oxoethoxy]ethyl]benzenesulfonamide\",0.3\nCOc1nccnc1NS(=O)(=O)c2ccc(N)cc2,\"InChI=1S/C11H12N4O3S/c1-18-11-10(13-6-7-14-11)15-19(16,17)9-4-2-8(12)3-5-9/h2-7H,12H2,1H3,(H,13,15)\",[C][O][C][=N][C][=C][N][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],4-amino-n-(3-methoxypyrazin-2-yl)benzenesulfonamide,-0.65\nCC(=O)Nc1cccc2c1c(c(C)n2CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3,\"InChI=1S/C19H17ClN2O5S/c1-11-19(28(26,27)14-8-6-13(20)7-9-14)18-15(21-12(2)23)4-3-5-16(18)22(11)10-17(24)25/h3-9H,10H2,1-2H3,(H,21,23)(H,24,25)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][=Branch1][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[4-acetamido-3-(4-chlorophenyl)sulfonyl-2-methylindol-1-yl]acetic acid,0.4\nNC1CCc2cc(OC(=O)c3ccccc3)c(OC(=O)c4ccccc4)cc2C1,\"InChI=1S/C24H21NO4/c25-20-12-11-18-14-21(28-23(26)16-7-3-1-4-8-16)22(15-19(18)13-20)29-24(27)17-9-5-2-6-10-17/h1-10,14-15,20H,11-13,25H2\",[N][C][C][C][C][=C][C][Branch1][=C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][=C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch2][C][Ring2][Ring1][N],\"[7-amino-3-(benzoyloxy)-5,6,7,8-tetrahydronaphthalen-2-yl] benzoate\",2.6\nCC(C)C(=O)Nc1ccc2C(=O)NC(=O)c2c1,\"InChI=1S/C12H12N2O3/c1-6(2)10(15)13-7-3-4-8-9(5-7)12(17)14-11(8)16/h3-6H,1-2H3,(H,13,15)(H,14,16,17)\",[C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O],\"n-(1,3-dioxoisoindol-5-yl)-2-methylpropanamide\",1.55\nCc1ccc(cc1)C(=O)c2cc(O)c(O)c(c2)[N+](=O)[O-],\"InChI=1S/C14H11NO5/c1-8-2-4-9(5-3-8)13(17)10-6-11(15(19)20)14(18)12(16)7-10/h2-7,16,18H,1H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][Branch1][C][O][=C][Branch1][C][O][C][=Branch1][Ring2][=C][Ring1][Branch2][N+1][=Branch1][C][=O][O-1],\"(3,4-dihydroxy-5-nitrophenyl)-(4-methylphenyl)methanone\",0.74\nCc1c(Oc2ccc(Cl)cc2)c3cc(F)ccc3n1CC(=O)O,\"InChI=1S/C17H13ClFNO3/c1-10-17(23-13-5-2-11(18)3-6-13)14-8-12(19)4-7-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\",[C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],2-[3-(4-chlorophenoxy)-5-fluoro-2-methylindol-1-yl]acetic acid,1.26\nCOc1ccc2SCC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1,\"InChI=1S/C24H30N4O4S/c1-30-19-2-3-23-20(13-19)28(24(29)16-33-23)9-8-27-6-4-17(5-7-27)25-14-18-12-21-22(15-26-18)32-11-10-31-21/h2-3,12-13,15,17,25H,4-11,14,16H2,1H3\",[C][O][C][=C][C][=C][S][C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C],\"4-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-6-methoxy-1,4-benzothiazin-3-one\",1.78\nCCOc1ccc(cc1)N2C(=O)c3ccccc3N=C2[C@@H](C)N(Cc4cccnc4)C(=O)Cc5ccc(cc5)C(F)(F)F,\"InChI=1S/C33H29F3N4O3/c1-3-43-27-16-14-26(15-17-27)40-31(38-29-9-5-4-8-28(29)32(40)42)22(2)39(21-24-7-6-18-37-20-24)30(41)19-23-10-12-25(13-11-23)33(34,35)36/h4-18,20,22H,3,19,21H2,1-2H3/t22-/m1/s1\",[C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][O][C@@H1][Branch1][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],n-[(1r)-1-[3-(4-ethoxyphenyl)-4-oxoquinazolin-2-yl]ethyl]-n-(pyridin-3-ylmethyl)-2-[4-(trifluoromethyl)phenyl]acetamide,4.25\nBrc1ccccc1C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C18H22BrNO/c19-16-4-2-1-3-15(16)17(21)20-11-18-8-12-5-13(9-18)7-14(6-12)10-18/h1-4,12-14H,5-11H2,(H,20,21)\",[Br][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-bromobenzamide,4.15\nCN1C(=O)CC(C1=O)c2ccccc2,\"InChI=1S/C11H11NO2/c1-12-10(13)7-9(11(12)14)8-5-3-2-4-6-8/h2-6,9H,7H2,1H3\",[C][N][C][=Branch1][C][=O][C][C][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-methyl-3-phenylpyrrolidine-2,5-dione\",0.68\nCSc1ccc(cc1)C(=O)C(C)(C)N2CCOCC2,\"InChI=1S/C15H21NO2S/c1-15(2,16-8-10-18-11-9-16)14(17)12-4-6-13(19-3)7-5-12/h4-7H,8-11H2,1-3H3\",[C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][N][C][C][O][C][C][Ring1][=Branch1],2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one,3.49\nCCN1C(=O)C=Cc2cnc(Nc3ccc(OC)c(OC)c3)nc12,\"InChI=1S/C17H18N4O3/c1-4-21-15(22)8-5-11-10-18-17(20-16(11)21)19-12-6-7-13(23-2)14(9-12)24-3/h5-10H,4H2,1-3H3,(H,18,19,20)\",[C][C][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Branch2][Ring1][C][N][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][N][=C][Ring2][Ring1][=Branch1][Ring1][P],\"2-[(3,4-dimethoxyphenyl)amino]-8-ethylpyrido[6,5-d]pyrimidin-7-one\",2.7\nCN(CCOc1ccc(NS(=O)(=O)C)cc1)CCc2ccc(NS(=O)(=O)C)cc2,\"InChI=1S/C19H27N3O5S2/c1-22(13-12-16-4-6-17(7-5-16)20-28(2,23)24)14-15-27-19-10-8-18(9-11-19)21-29(3,25)26/h4-11,20-21H,12-15H2,1-3H3\",[C][N][Branch2][Ring1][#Branch1][C][C][O][C][=C][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][Ring1][O][C][C][C][=C][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][Ring1][O],n-[4-[2-[2-(4-methanesulfonamidophenyl)ethyl-methylamino]ethoxy]phenyl]methanesulfonamide,0.6\nCCN1CCC[C@@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1,\"InChI=1S/C19H28Cl2N4O/c1-2-23-7-3-4-15(13-23)14-24-8-10-25(11-9-24)19(26)22-16-5-6-17(20)18(21)12-16/h5-6,12,15H,2-4,7-11,13-14H2,1H3,(H,22,26)/t15-/m1/s1\",[C][C][N][C][C][C][C@@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2],\"n-(3,4-dichlorophenyl)-4-[[(3r)-1-ethylpiperidin-3-yl]methyl]piperazine-1-carboxamide\",1.94\nCC(C)N1C(=O)N(C)C(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CCS(=O)(=O)C4,\"InChI=1S/C22H22F3N3O5S2/c1-12(2)28-20-17(18(29)26(3)21(28)31)16(19(30)27-8-9-35(32,33)11-27)15(34-20)10-13-6-4-5-7-14(13)22(23,24)25/h4-7,12H,8-11H2,1-3H3\",[C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][Ring1][#Branch1],\"5-(1,1-dioxo1,3-thiazolidine-3-carbonyl)-3-methyl-1-propan-2-yl-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\",2.55\nCOc1cc(OC)cc(c1)C2=CC=C(NC(=O)OCc3ccccc3)C(=O)N2CC(=O)NC(C(C)C)C(=O)C(F)(F)F,\"InChI=1S/C29H30F3N3O7/c1-17(2)25(26(37)29(30,31)32)34-24(36)15-35-23(19-12-20(40-3)14-21(13-19)41-4)11-10-22(27(35)38)33-28(39)42-16-18-8-6-5-7-9-18/h5-14,17,25H,15-16H2,1-4H3,(H,33,39)(H,34,36)\",[C][O][C][=C][C][Branch1][Ring1][O][C][=C][C][=Branch1][Ring2][=C][Ring1][Branch2][C][=C][C][=C][Branch1][S][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[6-(3,5-dimethoxyphenyl)-2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyridin-3-yl]carbamate\",2.26\nCOc1cc2c(Nc3ncc(NC(=O)c4ccccc4)cn3)ncnc2cc1OCCCN5CCOCC5,\"InChI=1S/C27H29N7O4/c1-36-23-14-21-22(15-24(23)38-11-5-8-34-9-12-37-13-10-34)30-18-31-25(21)33-27-28-16-20(17-29-27)32-26(35)19-6-3-2-4-7-19/h2-4,6-7,14-18H,5,8-13H2,1H3,(H,32,35)(H,28,29,30,31,33)\",[C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][Ring1][#C][N][=C][N][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1],n-[2-[[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-yl]amino]pyrimidin-5-yl]benzamide,2.32\nCOc1cnc(nc1Oc2ccc(F)cc2F)c3ccccn3,\"InChI=1S/C16H11F2N3O2/c1-22-14-9-20-15(12-4-2-3-7-19-12)21-16(14)23-13-6-5-10(17)8-11(13)18/h2-9H,1H3\",[C][O][C][=C][N][=C][Branch2][Ring1][C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C][=C][C][=C][C][=N][Ring1][=Branch1],\"4-(2,4-difluorophenoxy)-5-methoxy-2-pyridin-2-ylpyrimidine\",3.1\nNC(=O)c1c(N)sc2CCCCc12,\"InChI=1S/C9H12N2OS/c10-8(12)7-5-3-1-2-4-6(5)13-9(7)11/h1-4,11H2,(H2,10,12)\",[N][C][=Branch1][C][=O][C][=C][Branch1][C][N][S][C][C][C][C][C][C][Ring1][#Branch2][=Ring1][=Branch1],\"2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide\",1.84\nFC(F)(F)c1nnc2ccc(nn12)N3CCCCCC3,\"InChI=1S/C12H14F3N5/c13-12(14,15)11-17-16-9-5-6-10(18-20(9)11)19-7-3-1-2-4-8-19/h5-6H,1-4,7-8H2\",[F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][C][C][C][C][C][Ring1][#Branch1],\"6-(azepan-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\",3.29\nOCCN(C(=O)CNC(=O)c1cc2cc(Cl)ccc2[nH]1)c3ccccc3,\"InChI=1S/C19H18ClN3O3/c20-14-6-7-16-13(10-14)11-17(22-16)19(26)21-12-18(25)23(8-9-24)15-4-2-1-3-5-15/h1-7,10-11,22,24H,8-9,12H2,(H,21,26)\",[O][C][C][N][Branch2][Ring1][O][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1],5-chloro-n-[2-(2-hydroxyethyl-phenylamino)-2-oxoethyl]-1h-indole-2-carboxamide,3.37\nCCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cc(F)cc(F)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H38F2N2O5S2/c1-4-36(32(37)19-23-5-9-29(10-6-23)42(2,38)39)28-13-16-35(17-14-28)18-15-31(25-20-26(33)22-27(34)21-25)24-7-11-30(12-8-24)43(3,40)41/h5-12,20-22,28,31H,4,13-19H2,1-3H3/t31-/m1/s1\",[C][C][N][Branch2][Branch1][Ring1][C][C][C][N][Branch2][Ring2][#Branch1][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][C][C][Ring2][Ring1][O][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],\"n-[1-[(3r)-3-(3,5-difluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide\",2.2\nCNc1nc2ccccc2n1Cc3sc4N(CC(C)C)C(=O)N(C)C(=O)c4c3C(=O)N5C[C@H](O)CO5,\"InChI=1S/C24H28N6O5S/c1-13(2)9-29-22-19(20(32)27(4)24(29)34)18(21(33)30-10-14(31)12-35-30)17(36-22)11-28-16-8-6-5-7-15(16)26-23(28)25-3/h5-8,13-14,31H,9-12H2,1-4H3,(H,25,26)/t14-/m0/s1\",[C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][S][C][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=Ring1][=N][C][=Ring1][S][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][O][Ring1][=Branch1],\"5-[(4s)-4-hydroxy1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(2-methylaminobenzimidazol-1-yl)methyl]-1-(2-methylpropyl)thieno[3,2-e]pyrimidine-2,4-dione\",1.77\nCCN(CC)Cc1cc(Nc2ccnc3cc(Cl)ccc23)ccc1O,\"InChI=1S/C20H22ClN3O/c1-3-24(4-2)13-14-11-16(6-8-20(14)25)23-18-9-10-22-19-12-15(21)5-7-17(18)19/h5-12,25H,3-4,13H2,1-2H3,(H,22,23)\",[C][C][N][Branch1][Ring1][C][C][C][C][=C][C][Branch2][Ring1][Ring1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1][=C][C][=C][Ring2][Ring1][C][O],4-[(7-chloroquinolin-4-yl)amino]-2-(diethylaminomethyl)phenol,2.9\nFc1ccccc1Nc2oc(nn2)C(=O)Nc3ccc(N4CCOCC4)c(F)c3,\"InChI=1S/C19H17F2N5O3/c20-13-3-1-2-4-15(13)23-19-25-24-18(29-19)17(27)22-12-5-6-16(14(21)11-12)26-7-9-28-10-8-26/h1-6,11H,7-10H2,(H,22,27)(H,23,25)\",[F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][=C][Ring1][=N],\"n-(3-fluoro-4-morpholin-4-ylphenyl)-5-[(2-fluorophenyl)amino]-1,3,4-oxadiazole-2-carboxamide\",3.6\nCC1=NS(=O)(=O)c2cc(Cl)ccc2N1,\"InChI=1S/C8H7ClN2O2S/c1-5-10-7-3-2-6(9)4-8(7)14(12,13)11-5/h2-4H,1H3,(H,10,11)\",[C][C][=N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring1][=N],\"7-chloro-3-methyl-4h-benzo[e][1,2,4]thiadiazine 1,1-dioxide\",1.05\nCN(Cc1oc2ccccc2c1C)C(=O)\\C=C\\c3cnc4NC(=O)CCc4c3,\"InChI=1S/C22H21N3O3/c1-14-17-5-3-4-6-18(17)28-19(14)13-25(2)21(27)10-7-15-11-16-8-9-20(26)24-22(16)23-12-15/h3-7,10-12H,8-9,13H2,1-2H3,(H,23,24,26)/b10-7+\",[C][N][Branch1][S][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][=Branch1][C][=O][\\C][=C][\\C][=C][N][=C][N][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][=C][Ring1][O],\"(e)-n-methyl-n-[(3-methyl-1-benzofuran-2-yl)methyl]-3-(7-oxo-6,8-dihydro-5h-1,8-naphthyridin-3-yl)prop-2-enamide\",2.36\nFc1ccc(F)c(NS(=O)(=O)c2ccc(Cl)cc2)c1,\"InChI=1S/C12H8ClF2NO2S/c13-8-1-4-10(5-2-8)19(17,18)16-12-7-9(14)3-6-11(12)15/h1-7,16H\",[F][C][=C][C][=C][Branch1][C][F][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][C],\"4-chloro-n-(2,5-difluorophenyl)benzenesulfonamide\",2.9\nCOC(=O)N1CCN([C@H](CN2CCCC2)C1)C(=O)Cc3ccc(Cl)c(Cl)c3,\"InChI=1S/C19H25Cl2N3O3/c1-27-19(26)23-8-9-24(15(13-23)12-22-6-2-3-7-22)18(25)11-14-4-5-16(20)17(21)10-14/h4-5,10,15H,2-3,6-9,11-13H2,1H3/t15-/m1/s1\",[C][O][C][=Branch1][C][=O][N][C][C][N][Branch1][#C][C@H1][Branch1][=Branch2][C][N][C][C][C][C][Ring1][Branch1][C][Ring1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"methyl (3r)-4-[2-(3,4-dichlorophenyl)acetyl]-3-(pyrrolidin-1-ylmethyl)piperazine-1-carboxylate\",2.05\nCCN(C(=O)Nc1ccccc1)c2ccccc2,\"InChI=1S/C15H16N2O/c1-2-17(14-11-7-4-8-12-14)15(18)16-13-9-5-3-6-10-13/h3-12H,2H2,1H3,(H,16,18)\",[C][C][N][Branch1][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-ethyl-1,3-di(phenyl)urea\",3.1\nClc1ccc2[nH]c(cc2c1)C(=O)N3CCNCC3,\"InChI=1S/C13H14ClN3O/c14-10-1-2-11-9(7-10)8-12(16-11)13(18)17-5-3-15-4-6-17/h1-2,7-8,15-16H,3-6H2\",[Cl][C][=C][C][=C][NH1][C][=Branch1][Branch2][=C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][N][C][C][Ring1][=Branch1],(5-chloro-1h-indol-2-yl)-piperazin-1-ylmethanone,1.65\nO=C(Nc1cccnc1C(=O)NCC2CCOCC2)c3cccc4ccccc34,\"InChI=1S/C23H23N3O3/c27-22(19-8-3-6-17-5-1-2-7-18(17)19)26-20-9-4-12-24-21(20)23(28)25-15-16-10-13-29-14-11-16/h1-9,12,16H,10-11,13-15H2,(H,25,28)(H,26,27)\",[O][=C][Branch2][Ring1][Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],3-(naphthalene-1-carbonylamino)-n-(oxan-4-ylmethyl)pyridine-2-carboxamide,4.4\nCOc1cnc(nc1NC(C)C)c2ccccn2,\"InChI=1S/C13H16N4O/c1-9(2)16-13-11(18-3)8-15-12(17-13)10-6-4-5-7-14-10/h4-9H,1-3H3,(H,15,16,17)\",[C][O][C][=C][N][=C][Branch1][O][N][=C][Ring1][=Branch1][N][C][Branch1][C][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1],5-methoxy-n-propan-2-yl-2-pyridin-2-ylpyrimidin-4-amine,2.01\nCCN(CC)CCNC(=O)c1cc(ccc1OC)S(=O)(=O)C,\"InChI=1S/C15H24N2O4S/c1-5-17(6-2)10-9-16-15(18)13-11-12(22(4,19)20)7-8-14(13)21-3/h7-8,11H,5-6,9-10H2,1-4H3,(H,16,18)\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][C],n-(2-diethylaminoethyl)-2-methoxy-5-methylsulfonylbenzamide,-0.9\nCC(C)N1CCC[C@H](CN2C(=O)c3cc(ccc3N=C2C(C)C)c4ccc(F)cc4)C1,\"InChI=1S/C26H32FN3O/c1-17(2)25-28-24-12-9-21(20-7-10-22(27)11-8-20)14-23(24)26(31)30(25)16-19-6-5-13-29(15-19)18(3)4/h7-12,14,17-19H,5-6,13,15-16H2,1-4H3/t19-/m0/s1\",[C][C][Branch1][C][C][N][C][C][C][C@H1][Branch2][Ring2][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][O][C][Branch1][C][C][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Ring2][Ring1][N],6-(4-fluorophenyl)-2-propan-2-yl-3-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]quinazolin-4-one,3.6\nBrc1ccc(s1)N2C[C@@]3(CN4CCC3CC4)OC2=O,\"InChI=1S/C13H15BrN2O2S/c14-10-1-2-11(19-10)16-8-13(18-12(16)17)7-15-5-3-9(13)4-6-15/h1-2,9H,3-8H2/t13-/m1/s1\",[Br][C][=C][C][=C][Branch1][Ring2][S][Ring1][Branch1][N][C][C@@][Branch1][N][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][O][C][Ring1][N][=O],\"(5r)-3-(5-bromothiophen-2-yl)spiro[1,3-oxazolidine-5,8'-1-azabicyclo[2.2.2]octane]-2-one\",2\nOC(=O)c1[nH]c2cc(Cl)cc(Cl)c2c1\\C=C\\3/CCN(C3=O)c4ccccc4,\"InChI=1S/C20H14Cl2N2O3/c21-12-9-15(22)17-14(18(20(26)27)23-16(17)10-12)8-11-6-7-24(19(11)25)13-4-2-1-3-5-13/h1-5,8-10,23H,6-7H2,(H,26,27)/b11-8+\",[O][C][=Branch1][C][=O][C][NH1][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=Ring1][O][\\C][=C][/C][C][N][Branch1][Branch1][C][\\-Ring1][Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4,6-dichloro-3-[(e)-(2-oxo-1-phenylpyrrolidin-3-ylidene)methyl]-1h-indole-2-carboxylic acid\",1.85\nCCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cc(F)cc(Cl)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H38ClFN2O5S2/c1-4-36(32(37)19-23-5-9-29(10-6-23)42(2,38)39)28-13-16-35(17-14-28)18-15-31(25-20-26(33)22-27(34)21-25)24-7-11-30(12-8-24)43(3,40)41/h5-12,20-22,28,31H,4,13-19H2,1-3H3/t31-/m1/s1\",[C][C][N][Branch2][Branch1][Ring1][C][C][C][N][Branch2][Ring2][#Branch1][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][C][Ring2][Ring1][O][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-[1-[(3r)-3-(3-chloro-5-fluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide,2.71\nCNC1CCN(C1)c2ccc(NC(=O)c3ccc(cc3)c4ccccc4)cn2,\"InChI=1S/C23H24N4O/c1-24-21-13-14-27(16-21)22-12-11-20(15-25-22)26-23(28)19-9-7-18(8-10-19)17-5-3-2-4-6-17/h2-12,15,21,24H,13-14,16H2,1H3,(H,26,28)\",[C][N][C][C][C][N][Branch1][Ring2][C][Ring1][Branch1][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][Ring2][Ring1][Branch1],n-[6-(3-methylaminopyrrolidin-1-yl)pyridin-3-yl]-4-phenylbenzamide,2.35\nFC1(F)Oc2ccc(\\C=C\\3/SC(=O)NC3=O)cc2O1,\"InChI=1S/C11H5F2NO4S/c12-11(13)17-6-2-1-5(3-7(6)18-11)4-8-9(15)14-10(16)19-8/h1-4H,(H,14,15,16)/b8-4-\",[F][C][Branch1][C][F][O][C][=C][C][=C][Branch1][=N][\\C][=C][/S][C][=Branch1][C][=O][N][C][\\-Ring1][=Branch1][=O][C][=C][Ring1][=C][O][Ring2][Ring1][C],\"(5z)-5-[(2,2-difluoro-1,3-benzodioxol-5-yl)methylidene]-1,3-thiazolidine-2,4-dione\",2.8\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3cc[n+]([O-])cc3)C(=O)C(F)(F)F,\"InChI=1S/C26H26F3N5O5/c1-16(2)22(23(36)26(27,28)29)32-21(35)15-34-20(18-6-4-3-5-7-18)9-8-19(24(34)37)31-25(38)30-14-17-10-12-33(39)13-11-17/h3-13,16,22H,14-15H2,1-2H3,(H,32,35)(H2,30,31,38)\",[C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=N+1][Branch1][C][O-1][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[3-[(1-oxidopyridin-1-ium-4-yl)methylcarbamoylamino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.13\nCOc1c(C)c2COC(=O)c2c(O)c1C\\C=C(/C)\\CCC(=O)OCCN3CCOCC3,\"InChI=1S/C23H31NO7/c1-15(5-7-19(25)30-13-10-24-8-11-29-12-9-24)4-6-17-21(26)20-18(14-31-23(20)27)16(2)22(17)28-3/h4,26H,5-14H2,1-3H3/b15-4+\",[C][O][C][=C][Branch1][C][C][C][C][O][C][=Branch1][C][=O][C][=Ring1][=Branch1][C][Branch1][C][O][=C][Ring1][N][C][\\C][=C][Branch1][C][/C][\\C][C][C][=Branch1][C][=O][O][C][C][N][C][C][O][C][C][Ring1][=Branch1],\"2-morpholin-4-ylethyl (e)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-4-methylhex-4-enoate\n2-morpholin-4-ylethyl 6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-4-methylhex-4-enoate\",2.26\nOC1CS(=O)(=O)CC1N2CCC(CC2)c3ccccc3,\"InChI=1S/C15H21NO3S/c17-15-11-20(18,19)10-14(15)16-8-6-13(7-9-16)12-4-2-1-3-5-12/h1-5,13-15,17H,6-11H2\",[O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Ring1][#Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1,1-dioxo-4-(4-phenylpiperidin-1-yl)thiolan-3-ol\",1.4\nCOc1ccc2[nH]c(cc2c1)C(=O)N3CCN(C)CC3,\"InChI=1S/C15H19N3O2/c1-17-5-7-18(8-6-17)15(19)14-10-11-9-12(20-2)3-4-13(11)16-14/h3-4,9-10,16H,5-8H2,1-2H3\",[C][O][C][=C][C][=C][NH1][C][=Branch1][Branch2][=C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1],(5-methoxy-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone,1.62\nCC(C)C1NCCc2c1sc3ccccc23,\"InChI=1S/C14H17NS/c1-9(2)13-14-11(7-8-15-13)10-5-3-4-6-12(10)16-14/h3-6,9,13,15H,7-8H2,1-2H3\",[C][C][Branch1][C][C][C][N][C][C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1],\"1-propan-2-yl-1,2,3,4-tetrahydro-[1]benzothiolo[2,3-c]pyridine\",2.8\nNc1nc(Nc2ccc(cc2)S(=O)(=O)N)nn1C(=O)c3c(F)cccc3F,\"InChI=1S/C15H12F2N6O3S/c16-10-2-1-3-11(17)12(10)13(24)23-14(18)21-15(22-23)20-8-4-6-9(7-5-8)27(19,25)26/h1-7H,(H2,19,25,26)(H3,18,20,21,22)\",[N][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][N][Ring1][S][C][=Branch1][C][=O][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F],\"4-[[5-amino-1-(2,6-difluorobenzoyl)-1,2,4-triazol-3-yl]amino]benzenesulfonamide\",1.87\nCCCCCc1ccc(cc1)c2nnc(N)s2,\"InChI=1S/C13H17N3S/c1-2-3-4-5-10-6-8-11(9-7-10)12-15-16-13(14)17-12/h6-9H,2-5H2,1H3,(H2,14,16)\",[C][C][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1],\"5-(4-pentylphenyl)-1,3,4-thiadiazol-2-amine\",4.13\nCc1sc2ncnc(SCC(=O)N3CCCC3)c2c1C,\"InChI=1S/C14H17N3OS2/c1-9-10(2)20-14-12(9)13(15-8-16-14)19-7-11(18)17-5-3-4-6-17/h8H,3-7H2,1-2H3\",[C][C][S][C][=N][C][=N][C][Branch1][=C][S][C][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=C][Ring1][#C][C][=Ring2][Ring1][C][C],\"2-(5,6-dimethylthieno[3,2-e]pyrimidin-4-yl)sulfanyl-1-pyrrolidin-1-ylethanone\",2.89\nFC(F)(F)c1nnc2ccc(NCn3nnc4ccccc34)nn12,\"InChI=1S/C13H9F3N8/c14-13(15,16)12-20-19-11-6-5-10(21-24(11)12)17-7-23-9-4-2-1-3-8(9)18-22-23/h1-6H,7H2,(H,17,21)\",[F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][Branch1][S][N][C][N][N][=N][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][=N][N][Ring2][Ring1][Ring2][Ring1][P],\"n-(benzotriazol-1-ylmethyl)-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazin-6-amine\",2.34\nCCCN(CCC)S(=O)(=O)c1ccc(cc1)C(=O)O,\"InChI=1S/C13H19NO4S/c1-3-9-14(10-4-2)19(17,18)12-7-5-11(6-8-12)13(15)16/h5-8H,3-4,9-10H2,1-2H3,(H,15,16)\",[C][C][C][N][Branch1][Ring2][C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O],4-(dipropylsulfamoyl)benzoic acid,0.03\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)C)C(=O)C(F)(F)F,\"InChI=1S/C21H22F3N3O4/c1-12(2)18(19(30)21(22,23)24)26-17(29)11-27-16(14-7-5-4-6-8-14)10-9-15(20(27)31)25-13(3)28/h4-10,12,18H,11H2,1-3H3,(H,25,28)(H,26,29)\",[C][C][Branch1][C][C][C][Branch2][Ring2][C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-(3-acetamido-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.78\nCN(C)CCCN1c2ccccc2CCc3ccc(Cl)cc13,\"InChI=1S/C19H23ClN2/c1-21(2)12-5-13-22-18-7-4-3-6-15(18)8-9-16-10-11-17(20)14-19(16)22/h3-4,6-7,10-11,14H,5,8-9,12-13H2,1-2H3\",[C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][S][Ring1][#Branch1],\"3-(9-chloro-5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n,n-dimethylpropan-1-amine\",3.36\nOC(=O)c1ccccc1C2=C3C=CC(=O)C=C3Oc4cc(O)ccc24,\"InChI=1S/C20H12O5/c21-11-5-7-15-17(9-11)25-18-10-12(22)6-8-16(18)19(15)13-3-1-2-4-14(13)20(23)24/h1-10,21H,(H,23,24)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Ring1][#Branch1][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][S][Ring1][#Branch1],2-(3-hydroxy-6-oxoxanthen-9-yl)benzoic acid,0\nCOc1ccc(OC)c(c1)C(O)CNC(=O)CN,\"InChI=1S/C12H18N2O4/c1-17-8-3-4-11(18-2)9(5-8)10(15)7-14-12(16)6-13/h3-5,10,15H,6-7,13H2,1-2H3,(H,14,16)\",[C][O][C][=C][C][=C][Branch1][Ring1][O][C][C][=Branch1][Ring2][=C][Ring1][Branch2][C][Branch1][C][O][C][N][C][=Branch1][C][=O][C][N],\"2-amino-n-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]acetamide\",-0.71\nC[C@H](C(=O)O)c1cccc(c1)C(=O)c2ccccc2,\"InChI=1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)/t11-/m0/s1\",[C][C@H1][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],(2s)-2-[3-(benzoyl)phenyl]propanoic acid,-0.06\nO=C(NC1CCCCC1)C2CCCN(C2)S(=O)(=O)c3cccs3,\"InChI=1S/C16H24N2O3S2/c19-16(17-14-7-2-1-3-8-14)13-6-4-10-18(12-13)23(20,21)15-9-5-11-22-15/h5,9,11,13-14H,1-4,6-8,10,12H2,(H,17,19)\",[O][=C][Branch1][#Branch2][N][C][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][N][Branch1][Ring2][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][S][Ring1][Branch1],n-cyclohexyl-1-thiophen-2-ylsulfonylpiperidine-3-carboxamide,2.93\nCCC(N1NC(=O)C2=C(C1=O)C(=O)c3ccc(Cl)cc3N2)c4ccncc4,\"InChI=1S/C19H15ClN4O3/c1-2-14(10-5-7-21-8-6-10)24-19(27)15-16(18(26)23-24)22-13-9-11(20)3-4-12(13)17(15)25/h3-9,14H,2H2,1H3,(H,22,25)(H,23,26)\",[C][C][C][Branch2][Ring1][P][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][=C][C][=N][C][=C][Ring1][=Branch1],\"7-chloro-2-(1-pyridin-4-ylpropyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\",0.6\nCOC[C@@H](O)CN1C(=O)C=NN(C1=O)c2ccc(Cl)c(c2)C(=O)NCC3(O)CCCCCC3,\"InChI=1S/C22H29ClN4O6/c1-33-13-16(28)12-26-19(29)11-25-27(21(26)31)15-6-7-18(23)17(10-15)20(30)24-14-22(32)8-4-2-3-5-9-22/h6-7,10-11,16,28,32H,2-5,8-9,12-14H2,1H3,(H,24,30)/t16-/m0/s1\",[C][O][C][C@@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][=N][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][O][C][C][C][C][C][C][Ring1][Branch2],\"2-chloro-n-[(1-hydroxycycloheptyl)methyl]-5-[4-[(2s)-2-hydroxy-3-methoxypropyl]-3,5-dioxo-1,2,4-triazin-2-yl]benzamide\",1.44\nCCNc1nc(N)c(s1)C(=O)c2ccc(Cl)s2,\"InChI=1S/C10H10ClN3OS2/c1-2-13-10-14-9(12)8(17-10)7(15)5-3-4-6(11)16-5/h3-4H,2,12H2,1H3,(H,13,14)\",[C][C][N][C][=N][C][Branch1][C][N][=C][Branch1][Ring2][S][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1],\"(4-amino-2-ethylamino-1,3-thiazol-5-yl)-(5-chlorothiophen-2-yl)methanone\",3.63\nOc1ccc(cc1)N2C(=O)c3ccc(O)cc3C2=O,\"InChI=1S/C14H9NO4/c16-9-3-1-8(2-4-9)15-13(18)11-6-5-10(17)7-12(11)14(15)19/h1-7,16-17H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Ring1][O][=O],\"5-hydroxy-2-(4-hydroxyphenyl)isoindole-1,3-dione\",1.8\nC1CCC(CC1)NC2CCCCC2,\"InChI=1S/C12H23N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h11-13H,1-10H2\",[C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][C][C][C][Ring1][=Branch1],n-cyclohexylcyclohexanamine,-0.38\nOc1ccc(Br)cc1C(=O)C(=O)c2cc(Br)ccc2O,\"InChI=1S/C14H8Br2O4/c15-7-1-3-11(17)9(5-7)13(19)14(20)10-6-8(16)2-4-12(10)18/h1-6,17-18H\",[O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][Branch1][C][Br][=C][C][=C][Ring1][#Branch1][O],\"1,2-bis(5-bromo-2-hydroxyphenyl)ethane-1,2-dione\",3.85\nCC[C@H](CO)Nc1nc(SCc2ccccc2)nc3nc(N)sc13,\"InChI=1S/C16H19N5OS2/c1-2-11(8-22)18-13-12-14(19-15(17)24-12)21-16(20-13)23-9-10-6-4-3-5-7-10/h3-7,11,22H,2,8-9H2,1H3,(H3,17,18,19,20,21)/t11-/m1/s1\",[C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][C][=Ring1][=Branch1],\"(2r)-2-[[2-amino-5-(phenylmethylsulfanyl)-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]butan-1-ol\",3.27\nCC(N)COc1c(C)cccc1C,\"InChI=1S/C11H17NO/c1-8-5-4-6-9(2)11(8)13-7-10(3)12/h4-6,10H,7,12H2,1-3H3\",[C][C][Branch1][C][N][C][O][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C],\"1-(2,6-dimethylphenoxy)propan-2-amine\",0.62\nCCCCC(O)c1[nH]c2cc(C)c(cc2c1CCc3ccccc3)C(=O)O,\"InChI=1S/C23H27NO3/c1-3-4-10-21(25)22-17(12-11-16-8-6-5-7-9-16)19-14-18(23(26)27)15(2)13-20(19)24-22/h5-9,13-14,21,24-25H,3-4,10-12H2,1-2H3,(H,26,27)\",[C][C][C][C][C][Branch1][C][O][C][NH1][C][=C][C][Branch1][C][C][=C][Branch2][Ring1][C][C][=C][Ring1][#Branch1][C][=Ring1][#Branch2][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O],2-(1-hydroxypentyl)-6-methyl-3-(2-phenylethyl)-1h-indole-5-carboxylic acid,2.59\nCC(C(=O)Nc1ccc(Cl)cc1)c2ncc(cc2Cl)C(F)(F)F,\"InChI=1S/C15H11Cl2F3N2O/c1-8(14(23)22-11-4-2-10(16)3-5-11)13-12(17)6-9(7-21-13)15(18,19)20/h2-8H,1H3,(H,22,23)\",[C][C][Branch1][P][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=N][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F],n-(4-chlorophenyl)-2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]propanamide,4.19\nCN(CCOc1ccc(C[C@H](Nc2ccccc2C(=O)c3ccccc3)C(=O)O)cc1)c4ccccn4,\"InChI=1S/C30H29N3O4/c1-33(28-13-7-8-18-31-28)19-20-37-24-16-14-22(15-17-24)21-27(30(35)36)32-26-12-6-5-11-25(26)29(34)23-9-3-2-4-10-23/h2-18,27,32H,19-21H2,1H3,(H,35,36)/t27-/m0/s1\",[C][N][Branch2][Ring2][#C][C][C][O][C][=C][C][=C][Branch2][Ring1][S][C][C@H1][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][#Branch2][C][=C][C][=C][C][=N][Ring1][=Branch1],(2s)-2-[[2-(benzoyl)phenyl]amino]-3-[4-[2-(methyl-pyridin-2-ylamino)ethoxy]phenyl]propanoic acid,2.15\nCN(C)CC(O)COc1ccc(Nc2nccc(Nc3ccccc3)n2)cc1,\"InChI=1S/C21H25N5O2/c1-26(2)14-18(27)15-28-19-10-8-17(9-11-19)24-21-22-13-12-20(25-21)23-16-6-4-3-5-7-16/h3-13,18,27H,14-15H2,1-2H3,(H2,22,23,24,25)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch1][N][C][=N][C][=C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N][C][=C][Ring2][Ring1][Ring2],1-dimethylamino-3-[4-[[4-(phenylamino)pyrimidin-2-yl]amino]phenoxy]propan-2-ol,1.58\nOC(=O)C1=CN(C2CC2)c3cc(N4CCNCC4)c(F)cc3C1=O,\"InChI=1S/C17H18FN3O3/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24/h7-10,19H,1-6H2,(H,23,24)\",[O][C][=Branch1][C][=O][C][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][=C][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][=C][Branch1][C][F][C][=C][Ring1][=N][C][Ring2][Ring1][Ring2][=O],1-cyclopropyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid,-0.96\nCN(C)C(=O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)c2cc3cc(Cl)ccc3[nH]2,\"InChI=1S/C21H22ClN3O3/c1-25(2)21(28)19(26)17(10-13-6-4-3-5-7-13)24-20(27)18-12-14-11-15(22)8-9-16(14)23-18/h3-9,11-12,17,19,23,26H,10H2,1-2H3,(H,24,27)/t17-,19+/m0/s1\",[C][N][Branch1][C][C][C][=Branch1][C][=O][C@H1][Branch1][C][O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],\"5-chloro-n-[(2s,3r)-4-dimethylamino-3-hydroxy-4-oxo-1-phenylbutan-2-yl]-1h-indole-2-carboxamide\",3.6\nCCc1nc2c(N)nc3ccccc3c2n1CC(C)C,\"InChI=1S/C16H20N4/c1-4-13-19-14-15(20(13)9-10(2)3)11-7-5-6-8-12(11)18-16(14)17/h5-8,10H,4,9H2,1-3H3,(H2,17,18)\",[C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][C],\"2-ethyl-1-(2-methylpropyl)imidazo[4,5-c]quinolin-4-amine\",2.55\nCCN[C@H]1C[C@H](C)S(=O)(=O)c2sc(cc12)S(=O)(=O)N,\"InChI=1S/C10H16N2O4S3/c1-3-12-8-4-6(2)18(13,14)10-7(8)5-9(17-10)19(11,15)16/h5-6,8,12H,3-4H2,1-2H3,(H2,11,15,16)/t6-,8-/m0/s1\",[C][C][N][C@H1][C][C@H1][Branch1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][S][C][=Branch1][#Branch1][=C][C][Ring1][N][=Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N],\"(4s,6s)-4-ethylamino-6-methyl-7,7-dioxo-5,6-dihydro-4h-thieno[5,4-b]thiopyran-2-sulfonamide\",0.27\nCCCNC(=O)c1nnc2c(cccc2c1N)c3cnccc3OC,\"InChI=1S/C18H19N5O2/c1-3-8-21-18(24)17-15(19)12-6-4-5-11(16(12)22-23-17)13-10-20-9-7-14(13)25-2/h4-7,9-10H,3,8H2,1-2H3,(H2,19,22)(H,21,24)\",[C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][N][=C][C][=C][Ring1][=Branch1][O][C],4-amino-8-(4-methoxypyridin-3-yl)-n-propylcinnoline-3-carboxamide,2.83\nCC(N)Cc1c[nH]c2ccc(OCc3cccs3)cc12,\"InChI=1S/C16H18N2OS/c1-11(17)7-12-9-18-16-5-4-13(8-15(12)16)19-10-14-3-2-6-20-14/h2-6,8-9,11,18H,7,10,17H2,1H3\",[C][C][Branch1][C][N][C][C][=C][NH1][C][=C][C][=C][Branch1][#Branch2][O][C][C][=C][C][=C][S][Ring1][Branch1][C][=C][Ring1][S][Ring1][=N],1-[5-(thiophen-2-ylmethoxy)-1h-indol-3-yl]propan-2-amine,0.48\nC1CC2(CCN1)OC(c3ccccc3)c4ccccc24,\"InChI=1S/C18H19NO/c1-2-6-14(7-3-1)17-15-8-4-5-9-16(15)18(20-17)10-12-19-13-11-18/h1-9,17,19H,10-13H2\",[C][C][C][Branch1][=Branch1][C][C][N][Ring1][=Branch1][O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1],\"1-phenylspiro[1h-2-benzofuran-3,4'-piperidine]\",0.75\nCCN(C1CCN(CC[C@@H](c2ccccc2)c3ccc(cc3)S(=O)(=O)C)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H40N2O5S2/c1-4-34(32(35)24-25-10-14-29(15-11-25)40(2,36)37)28-18-21-33(22-19-28)23-20-31(26-8-6-5-7-9-26)27-12-16-30(17-13-27)41(3,38)39/h5-17,28,31H,4,18-24H2,1-3H3/t31-/m0/s1\",[C][C][N][Branch2][Ring2][N][C][C][C][N][Branch2][Ring1][S][C][C][C@@H1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring2][Ring1][=Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[(3s)-3-(4-methylsulfonylphenyl)-3-phenylpropyl]piperidin-4-yl]acetamide,1.38\nCN1CCN(CC1)C2=Nc3ccccc3Oc4ccc(Cl)cc24,\"InChI=1S/C18H18ClN3O/c1-21-8-10-22(11-9-21)18-14-12-13(19)6-7-16(14)23-17-5-3-2-4-15(17)20-18/h2-7,12H,8-11H2,1H3\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][S][Ring1][#Branch1],\"8-chloro-6-(4-methylpiperazin-1-yl)benzo[b][1,5]benzoxazepine\",3.24\nCN(C)CCCn1c2CCCCCCc2c3ccccc13,\"InChI=1S/C19H28N2/c1-20(2)14-9-15-21-18-12-6-4-3-5-10-16(18)17-11-7-8-13-19(17)21/h7-8,11,13H,3-6,9-10,12,14-15H2,1-2H3\",[C][N][Branch1][C][C][C][C][C][N][C][C][C][C][C][C][C][C][=Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],\"3-(6,7,8,9,10,11-hexahydrocycloocta[b]indol-5-yl)-n,n-dimethylpropan-1-amine\",2.96\nNC(=O)c1cccnc1Oc2ccccc2,\"InChI=1S/C12H10N2O2/c13-11(15)10-7-4-8-14-12(10)16-9-5-2-1-3-6-9/h1-8H,(H2,13,15)\",[N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(phenoxy)pyridine-3-carboxamide,1.13\nN(c1ccccc1)c2ccnc(Nc3ccccc3)n2,\"InChI=1S/C16H14N4/c1-3-7-13(8-4-1)18-15-11-12-17-16(20-15)19-14-9-5-2-6-10-14/h1-12H,(H2,17,18,19,20)\",[N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N],\"n,n'-di(phenyl)pyrimidine-2,4-diamine\",4.06\nCCN1CCC[C@H]1CNC(=O)c2cc(Br)cc(OC)c2OC,\"InChI=1S/C16H23BrN2O3/c1-4-19-7-5-6-12(19)10-18-16(20)13-8-11(17)9-14(21-2)15(13)22-3/h8-9,12H,4-7,10H2,1-3H3,(H,18,20)/t12-/m0/s1\",[C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Br][=C][C][Branch1][Ring1][O][C][=C][Ring1][=Branch2][O][C],\"5-bromo-n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2,3-dimethoxybenzamide\",1.2\nCCN(CC)C(=O)c1ccc(cc1)C2=CC3(CCNCC3)Oc4cccc(O)c24,\"InChI=1S/C24H28N2O3/c1-3-26(4-2)23(28)18-10-8-17(9-11-18)19-16-24(12-14-25-15-13-24)29-21-7-5-6-20(27)22(19)21/h5-11,16,25,27H,3-4,12-15H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][Branch2][C][C][N][C][C][Ring1][=Branch1][O][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][S][Ring1][#Branch1],\"n,n-diethyl-4-(5-hydroxyspiro[chromene-2,4'-piperidine]-4-yl)benzamide\",0.54\nCN(C)CC(O)COc1ccc(Nc2nccc(Nc3cccc(Cl)c3)n2)cc1,\"InChI=1S/C21H24ClN5O2/c1-27(2)13-18(28)14-29-19-8-6-16(7-9-19)25-21-23-11-10-20(26-21)24-17-5-3-4-15(22)12-17/h3-12,18,28H,13-14H2,1-2H3,(H2,23,24,25,26)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1],1-[4-[[4-[(3-chlorophenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol,2.5\nCC(=O)Nc1ccccc1C,\"InChI=1S/C9H11NO/c1-7-5-3-4-6-9(7)10-8(2)11/h3-6H,1-2H3,(H,10,11)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C],n-(2-methylphenyl)acetamide,1\nClc1ccc(OC2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C23H31ClN2O2/c24-21-2-1-19(28-18-3-5-25-6-4-18)10-20(21)22(27)26-14-23-11-15-7-16(12-23)9-17(8-15)13-23/h1-2,10,15-18,25H,3-9,11-14H2,(H,26,27)\",[Cl][C][=C][C][=C][Branch1][#Branch2][O][C][C][C][N][C][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chloro-5-piperidin-4-yloxybenzamide,1.83\nCOc1ccccc1CN2C(C(=O)NC3CCC(C)CC3)c4ccccc4C2=O,\"InChI=1S/C24H28N2O3/c1-16-11-13-18(14-12-16)25-23(27)22-19-8-4-5-9-20(19)24(28)26(22)15-17-7-3-6-10-21(17)29-2/h3-10,16,18,22H,11-15H2,1-2H3,(H,25,27)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][Branch1][P][C][=Branch1][C][=O][N][C][C][C][C][Branch1][C][C][C][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][Ring1][=O],2-[(2-methoxyphenyl)methyl]-n-(4-methylcyclohexyl)-3-oxo-1h-isoindole-1-carboxamide,3.74\nC[C@@H](Oc1cccc2ncnc(Nc3ccc4c(cnn4Cc5ccccn5)c3)c12)C(=O)N(C)C,\"InChI=1S/C26H25N7O2/c1-17(26(34)32(2)3)35-23-9-6-8-21-24(23)25(29-16-28-21)31-19-10-11-22-18(13-19)14-30-33(22)15-20-7-4-5-12-27-20/h4-14,16-17H,15H2,1-3H3,(H,28,29,31)/t17-/m1/s1\",[C][C@@H1][Branch2][Ring2][=C][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][#Branch2][N][C][=C][C][=C][C][Branch1][#C][C][=N][N][Ring1][Branch1][C][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring1][S][=C][Ring2][Ring1][O][Ring2][Ring1][#Branch1][C][=Branch1][C][=O][N][Branch1][C][C][C],\"(2r)-n,n-dimethyl-2-[4-[[1-(pyridin-2-ylmethyl)indazol-5-yl]amino]quinazolin-5-yl]oxypropanamide\",2.89\nCOCCNC(=O)c1cccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)c1,\"InChI=1S/C22H19ClN4O5/c1-32-8-7-24-20(29)13-4-2-3-12(9-13)11-27-22(31)17-18(21(30)26-27)25-16-10-14(23)5-6-15(16)19(17)28/h2-6,9-10H,7-8,11H2,1H3,(H,24,29)(H,25,28)(H,26,30)\",[C][O][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][=C][Ring2][Ring1][=Branch2],\"3-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]-n-(2-methoxyethyl)benzamide\",1.2\nCCn1c2ccccc2c3cc(NC(=O)C)ccc13,\"InChI=1S/C16H16N2O/c1-3-18-15-7-5-4-6-13(15)14-10-12(17-11(2)19)8-9-16(14)18/h4-10H,3H2,1-2H3,(H,17,19)\",[C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][P][Ring1][#Branch2],n-(9-ethylcarbazol-3-yl)acetamide,3.5\nCc1c(Sc2ccc(Cl)cc2)c3c(Cl)cccc3n1CC(=O)O,\"InChI=1S/C17H13Cl2NO2S/c1-10-17(23-12-7-5-11(18)6-8-12)16-13(19)3-2-4-14(16)20(10)9-15(21)22/h2-8H,9H2,1H3,(H,21,22)\",[C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],2-[4-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid,2.15\nOc1cccc(c1)c2nc3ccc(O)cc3s2,\"InChI=1S/C13H9NO2S/c15-9-3-1-2-8(6-9)13-14-11-5-4-10(16)7-12(11)17-13/h1-7,15-16H\",[O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][S][Ring1][#Branch2],\"2-(3-hydroxyphenyl)-1,3-benzothiazol-6-ol\",3.7\nCc1ccc2c(c1)c(Sc3ccc(cc3)S(=O)(=O)C)c(C)n2CC(=O)O,\"InChI=1S/C19H19NO4S2/c1-12-4-9-17-16(10-12)19(13(2)20(17)11-18(21)22)25-14-5-7-15(8-6-14)26(3,23)24/h4-10H,11H2,1-3H3,(H,21,22)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch2][Ring1][Ring2][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch1][C][C][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O],\"2-[2,5-dimethyl-3-(4-methylsulfonylphenyl)sulfanylindol-1-yl]acetic acid\",-0.08\nCc1ccc(cc1S(=O)(=O)n2ccc(n2)c3c(C)nc4ccc(Br)cn34)[N+](=O)[O-],\"InChI=1S/C18H14BrN5O4S/c1-11-3-5-14(24(25)26)9-16(11)29(27,28)23-8-7-15(21-23)18-12(2)20-17-6-4-13(19)10-22(17)18/h3-10H,1-2H3\",[C][C][=C][C][=C][Branch2][Ring2][Branch2][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=Branch1][Ring2][=N][Ring1][Branch1][C][=C][Branch1][C][C][N][=C][C][=C][C][Branch1][C][Br][=C][N][Ring1][O][Ring1][#Branch1][N+1][=Branch1][C][=O][O-1],\"6-bromo-2-methyl-3-[1-(2-methyl-5-nitrophenyl)sulfonylpyrazol-3-yl]imidazo[1,2-a]pyridine\",3.52\nO=C1CC2(CCCC2)CC(=O)N1CCCCN3CCN(CC3)c4ncccn4,\"InChI=1S/C21H31N5O2/c27-18-16-21(6-1-2-7-21)17-19(28)26(18)11-4-3-10-24-12-14-25(15-13-24)20-22-8-5-9-23-20/h5,8-9H,1-4,6-7,10-17H2\",[O][=C][C][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][C][=Branch1][C][=O][N][Ring1][O][C][C][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=N][Ring1][=Branch1],\"8-[4-(4-pyrimidin-2-ylpiperazin-1-yl)butyl]-8-azaspiro[4.5]decane-7,9-dione\",2.19\nc1ccc2cnccc2c1,InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H,[C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],isoquinoline,1.6\nCC(C)n1c(C)ncc1c2nc(Nc3ccc(C(=O)NC4CCN(C)CC4)c(F)c3)ncc2F,\"InChI=1S/C24H29F2N7O/c1-14(2)33-15(3)27-13-21(33)22-20(26)12-28-24(31-22)30-17-5-6-18(19(25)11-17)23(34)29-16-7-9-32(4)10-8-16/h5-6,11-14,16H,7-10H2,1-4H3,(H,29,34)(H,28,30,31)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][#C][N][C][=C][C][=C][Branch1][P][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][Branch1][C][F][=C][Ring1][P][=N][C][=C][Ring2][Ring1][Branch2][F],2-fluoro-4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-(1-methylpiperidin-4-yl)benzamide,2.41\nCC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)C(=O)N4CCCN(C)CC4)ncc2F,\"InChI=1S/C24H30FN7O/c1-16(2)32-17(3)26-15-21(32)22-20(25)14-27-24(29-22)28-19-8-6-18(7-9-19)23(33)31-11-5-10-30(4)12-13-31/h6-9,14-16H,5,10-13H2,1-4H3,(H,27,28,29)\",[C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][Branch2][=N][C][=C][Ring2][Ring1][#Branch1][F],\"[4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]-(4-methyl-1,4-diazepan-1-yl)methanone\",2.02\nC[C@H](CO)Nc1nc(SCc2ccccc2)nc3nc(N)sc13,\"InChI=1S/C15H17N5OS2/c1-9(7-21)17-12-11-13(18-14(16)23-11)20-15(19-12)22-8-10-5-3-2-4-6-10/h2-6,9,21H,7-8H2,1H3,(H3,16,17,18,19,20)/t9-/m1/s1\",[C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][C][=Ring1][=Branch1],\"(2r)-2-[[2-amino-5-(phenylmethylsulfanyl)-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\",3.12\nCOc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OCCCN4CCOCC4,\"InChI=1S/C22H24ClFN4O3/c1-29-20-12-16-19(13-21(20)31-8-2-5-28-6-9-30-10-7-28)25-14-26-22(16)27-18-4-3-15(23)11-17(18)24/h3-4,11-14H,2,5-10H2,1H3,(H,25,26,27)\",[C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1],n-(4-chloro-2-fluorophenyl)-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-amine,3.4\nCCN(CC)CCNC(=O)c1cc(Br)c(N)cc1OC,\"InChI=1S/C14H22BrN3O2/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3/h8-9H,4-7,16H2,1-3H3,(H,17,19)\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Br][=C][Branch1][C][N][C][=C][Ring1][Branch2][O][C],4-amino-5-bromo-n-(2-diethylaminoethyl)-2-methoxybenzamide,0.54\nCc1ccc(NC(=O)C=C)cc1,\"InChI=1S/C10H11NO/c1-3-10(12)11-9-6-4-8(2)5-7-9/h3-7H,1H2,2H3,(H,11,12)\",[C][C][=C][C][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][O],n-(4-methylphenyl)prop-2-enamide,2.25\nCC(Cc1ccc(O)cc1)NCC(O)c2cc(O)cc(O)c2,\"InChI=1S/C17H21NO4/c1-11(6-12-2-4-14(19)5-3-12)18-10-17(22)13-7-15(20)9-16(21)8-13/h2-5,7-9,11,17-22H,6,10H2,1H3\",[C][C][Branch1][=N][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][N][C][C][Branch1][C][O][C][=C][C][Branch1][C][O][=C][C][Branch1][C][O][=C][Ring1][Branch2],\"5-[1-hydroxy-2-[1-(4-hydroxyphenyl)propan-2-ylamino]ethyl]benzene-1,3-diol\",-0.06\nCOc1cc2nc(nc(N)c2cc1OC)N3CCN(CC3)C(=O)c4occc4,\"InChI=1S/C19H21N5O4/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14/h3-4,9-11H,5-8H2,1-2H3,(H2,20,21,22)\",[C][O][C][=C][C][=N][C][=Branch1][#C][=N][C][Branch1][C][N][=C][Ring1][#Branch1][C][=C][Ring1][O][O][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1],\"[4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl]-furan-2-ylmethanone\",1.9\nCCCC(=O)C1(CCN(CC1)C(=O)[C@@H](Cc2ccc(OC)cc2)NC(=O)[C@@H](N)Cc3cncn3C)c4ccccc4,\"InChI=1S/C32H41N5O4/c1-4-8-29(38)32(24-9-6-5-7-10-24)15-17-37(18-16-32)31(40)28(19-23-11-13-26(41-3)14-12-23)35-30(39)27(33)20-25-21-34-22-36(25)2/h5-7,9-14,21-22,27-28H,4,8,15-20,33H2,1-3H3,(H,35,39)/t27-,28+/m0/s1\",[C][C][C][C][=Branch1][C][=O][C][Branch2][Ring2][S][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@@H1][Branch1][=C][C][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][N][C][=Branch1][C][=O][C@@H1][Branch1][C][N][C][C][=C][N][=C][N][Ring1][Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],(2s)-2-amino-n-[(2r)-1-(4-butanoyl-4-phenylpiperidin-1-yl)-3-(4-methoxyphenyl)-1-oxopropan-2-yl]-3-(3-methylimidazol-4-yl)propanamide,2.51\nCCN1C(=O)C=Cc2cc(COc3cc(F)cc(c3)C4(CCOCC4)OC)ccc12,\"InChI=1S/C24H26FNO4/c1-3-26-22-6-4-17(12-18(22)5-7-23(26)27)16-30-21-14-19(13-20(25)15-21)24(28-2)8-10-29-11-9-24/h4-7,12-15H,3,8-11,16H2,1-2H3\",[C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring1][N][C][O][C][=C][C][Branch1][C][F][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][Branch1][Branch2][C][C][O][C][C][Ring1][=Branch1][O][C][=C][C][=C][Ring2][Ring1][N][Ring2][Ring1][#Branch1],1-ethyl-6-[[3-fluoro-5-(4-methoxyoxan-4-yl)phenoxy]methyl]quinolin-2-one,3.89\nCC(=O)OCCn1c(Sc2nc3cccc(Cl)c3s2)nc4c(N)ncnc14,\"InChI=1S/C16H13ClN6O2S2/c1-8(24)25-6-5-23-14-11(13(18)19-7-20-14)22-15(23)27-16-21-10-4-2-3-9(17)12(10)26-16/h2-4,7H,5-6H2,1H3,(H2,18,19,20)\",[C][C][=Branch1][C][=O][O][C][C][N][C][Branch2][Ring1][C][S][C][=N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][S][Ring1][#Branch2][=N][C][=C][Branch1][C][N][N][=C][N][=C][Ring2][Ring1][Branch1][Ring1][#Branch1],\"2-[6-amino-8-[(7-chloro-1,3-benzothiazol-2-yl)sulfanyl]purin-9-yl]ethyl acetate\",3.16\nCN(C)CCCN1c2ccccc2Sc3ccccc13,\"InChI=1S/C17H20N2S/c1-18(2)12-7-13-19-14-8-3-5-10-16(14)20-17-11-6-4-9-15(17)19/h3-6,8-11H,7,12-13H2,1-2H3\",[C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1],\"n,n-dimethyl-3-phenothiazin-10-ylpropan-1-amine\",2.56\nCCc1cc(OCc2ccc(cc2)c3ccccc3c4nn[nH]n4)c5CCCCc5n1,\"InChI=1S/C25H25N5O/c1-2-19-15-24(22-9-5-6-10-23(22)26-19)31-16-17-11-13-18(14-12-17)20-7-3-4-8-21(20)25-27-29-30-28-25/h3-4,7-8,11-15H,2,5-6,9-10,16H2,1H3,(H,27,28,29,30)\",[C][C][C][=C][C][Branch2][Ring1][N][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][=N][NH1][N][=Ring1][Branch1][=C][C][C][C][C][C][Ring1][=Branch1][=N][Ring2][Ring1][=N],\"2-ethyl-4-[[4-[2-(2h-tetrazol-5-yl)phenyl]phenyl]methoxy]-5,6,7,8-tetrahydroquinoline\",1.7\nO=C(NCCCN1CCCCC1)C(c2ccccc2)c3ccccc3,\"InChI=1S/C22H28N2O/c25-22(23-15-10-18-24-16-8-3-9-17-24)21(19-11-4-1-5-12-19)20-13-6-2-7-14-20/h1-2,4-7,11-14,21H,3,8-10,15-18H2,(H,23,25)\",[O][=C][Branch1][=N][N][C][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2,2-di(phenyl)-n-(3-piperidin-1-ylpropyl)acetamide\",1.33\nCOc1cc(N2CCN(C)CC2)c3NC(=CC(=O)c3c1)C(=O)Nc4ccc(cc4)N5CCOCC5,\"InChI=1S/C26H31N5O4/c1-29-7-9-31(10-8-29)23-16-20(34-2)15-21-24(32)17-22(28-25(21)23)26(33)27-18-3-5-19(6-4-18)30-11-13-35-14-12-30/h3-6,15-17H,7-14H2,1-2H3,(H,27,33)(H,28,32)\",[C][O][C][=C][C][Branch1][N][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][N][C][=Branch1][=N][=C][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring2][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],6-methoxy-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)-4-oxo-1h-quinoline-2-carboxamide,2.7\nNC(=O)Nc1cc(sc1C(=O)N)c2ccccc2,\"InChI=1S/C12H11N3O2S/c13-11(16)10-8(15-12(14)17)6-9(18-10)7-4-2-1-3-5-7/h1-6H,(H2,13,16)(H3,14,15,17)\",[N][C][=Branch1][C][=O][N][C][C][=C][Branch1][#Branch2][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],3-(carbamoylamino)-5-phenylthiophene-2-carboxamide,2.43\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)c3cccc(NC(=O)C)c3)C(=O)C(F)(F)F,\"InChI=1S/C27H27F3N4O6S/c1-16(2)24(25(37)27(28,29)30)32-23(36)15-34-22(18-8-5-4-6-9-18)13-12-21(26(34)38)33-41(39,40)20-11-7-10-19(14-20)31-17(3)35/h4-14,16,24,33H,15H2,1-3H3,(H,31,35)(H,32,36)\",[C][C][Branch1][C][C][C][Branch2][Branch1][Ring2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][=C][Ring1][#Branch2][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"n-[3-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]sulfamoyl]phenyl]acetamide\",2.43\nCCN(c1ccccc1)c2cc(NC)[n+](C)c(C)n2,\"InChI=1S/C15H20N4/c1-5-19(13-9-7-6-8-10-13)15-11-14(16-3)18(4)12(2)17-15/h6-11H,5H2,1-4H3/p+1\",[C][C][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][Ring1][N][C][=N+1][Branch1][C][C][C][Branch1][C][C][=N][Ring1][#Branch2],\"n-ethyl-n',1,2-trimethyl-n-phenylpyrimidin-1-ium-4,6-diamine\",-0.91\nCc1csc(NC(=O)c2cc(Sc3nncn3C)ccc2N)n1,\"InChI=1S/C14H14N6OS2/c1-8-6-22-13(17-8)18-12(21)10-5-9(3-4-11(10)15)23-14-19-16-7-20(14)2/h3-7H,15H2,1-2H3,(H,17,18,21)\",[C][C][=C][S][C][Branch2][Ring1][#Branch2][N][C][=Branch1][C][=O][C][=C][C][Branch1][#Branch2][S][C][=N][N][=C][N][Ring1][Branch1][C][=C][C][=C][Ring1][=N][N][=N][Ring2][Ring1][=Branch1],\"2-amino-n-(4-methyl-1,3-thiazol-2-yl)-5-[(4-methyl-1,2,4-triazol-3-yl)sulfanyl]benzamide\",2.3\nCN1CCN(CC(=O)N2c3ccccc3C(=O)Nc4cccnc24)CC1,\"InChI=1S/C19H21N5O2/c1-22-9-11-23(12-10-22)13-17(25)24-16-7-3-2-5-14(16)19(26)21-15-6-4-8-20-18(15)24/h2-8H,9-13H2,1H3,(H,21,26)\",[C][N][C][C][N][Branch2][Ring1][=C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][S][Ring1][=Branch1][C][C][Ring2][Ring1][=Branch2],\"11-[2-(4-methylpiperazin-1-yl)acetyl]-5h-pyrido[2,3-b][1,4]benzodiazepin-6-one\",-0.49\nCc1cccc(n1)c2nn3CCCc3c2c4ccnc5ccc(cc45)C(=O)N,\"InChI=1S/C22H19N5O/c1-13-4-2-5-18(25-13)21-20(19-6-3-11-27(19)26-21)15-9-10-24-17-8-7-14(22(23)28)12-16(15)17/h2,4-5,7-10,12H,3,6,11H2,1H3,(H2,23,28)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=N][N][C][C][C][C][Ring1][Branch1][=C][Ring1][Branch2][C][=C][C][=N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N],\"4-[2-(6-methylpyridin-2-yl)-5,6-dihydro-4h-pyrrolo[2,1-e]pyrazol-3-yl]quinoline-6-carboxamide\",1.71\nCC1=C(Oc2c(cccc2C1=O)C(=O)OCCN3CCCCC3)c4ccccc4,\"InChI=1S/C24H25NO4/c1-17-21(26)19-11-8-12-20(23(19)29-22(17)18-9-4-2-5-10-18)24(27)28-16-15-25-13-6-3-7-14-25/h2,4-5,8-12H,3,6-7,13-16H2,1H3\",[C][C][=C][Branch2][Ring1][#C][O][C][=C][Branch1][O][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][=Branch1][C][=O][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-piperidin-1-ylethyl 3-methyl-4-oxo-2-phenylchromene-8-carboxylate,3.42\nNc1nc(N)c2cc(Br)ccc2n1,\"InChI=1S/C8H7BrN4/c9-4-1-2-6-5(3-4)7(10)13-8(11)12-6/h1-3H,(H4,10,11,12,13)\",[N][C][=N][C][Branch1][C][N][=C][C][=C][Branch1][C][Br][C][=C][C][Ring1][#Branch1][=N][Ring1][N],\"6-bromoquinazoline-2,4-diamine\",1.78\nCCC(=C)C(=O)c1ccc(OCC(=O)O)c(Cl)c1Cl,\"InChI=1S/C13H12Cl2O4/c1-3-7(2)13(18)8-4-5-9(12(15)11(8)14)19-6-10(16)17/h4-5H,2-3,6H2,1H3,(H,16,17)\",[C][C][C][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][O][C][C][=Branch1][C][=O][O][C][Branch1][C][Cl][=C][Ring1][N][Cl],\"2-[2,3-dichloro-4-(2-methylidenebutanoyl)phenoxy]acetic acid\",0.02\nCSc1ccc2Sc3ccccc3N(CCC4CCCCN4C)c2c1,\"InChI=1S/C21H26N2S2/c1-22-13-6-5-7-16(22)12-14-23-18-8-3-4-9-20(18)25-21-11-10-17(24-2)15-19(21)23/h3-4,8-11,15-16H,5-7,12-14H2,1-2H3\",[C][S][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][N][C][C][C][C][C][C][C][N][Ring1][=Branch1][C][C][Ring2][Ring1][Ring1][=C][Ring2][Ring1][#Branch1],10-[2-(1-methylpiperidin-2-yl)ethyl]-2-methylsulfanylphenothiazine,3.76\nCCCCCOC(=O)NC1=NC(=O)N(C=C1F)[C@@H]2O[C@H](C)[C@@H](O)[C@H]2O,\"InChI=1S/C15H22FN3O6/c1-3-4-5-6-24-15(23)18-12-9(16)7-19(14(22)17-12)13-11(21)10(20)8(2)25-13/h7-8,10-11,13,20-21H,3-6H2,1-2H3,(H,17,18,22,23)/t8-,10-,11-,13-/m1/s1\",[C][C][C][C][C][O][C][=Branch1][C][=O][N][C][=N][C][=Branch1][C][=O][N][Branch1][=Branch1][C][=C][Ring1][#Branch1][F][C@@H1][O][C@H1][Branch1][C][C][C@@H1][Branch1][C][O][C@H1][Ring1][#Branch1][O],\"pentyl n-[1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-methyloxolan-2-yl]-5-fluoro-2-oxopyrimidin-4-yl]carbamate\",0.67\nCOc1ccc(cc1OC)c2csc(NC(=O)c3c(C)onc3C)n2,\"InChI=1S/C17H17N3O4S/c1-9-15(10(2)24-20-9)16(21)19-17-18-12(8-25-17)11-5-6-13(22-3)14(7-11)23-4/h5-8H,1-4H3,(H,18,19,21)\",[C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=C][S][C][Branch1][P][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][O][N][=C][Ring1][=Branch1][C][=N][Ring1][#C],\"n-[4-(3,4-dimethoxyphenyl)-1,3-thiazol-2-yl]-3,5-dimethyl-1,2-oxazole-4-carboxamide\",3.16\nCS(=O)(=O)Cc1cc(nc(n1)c2ccccc2)N3CCOCC3,\"InChI=1S/C16H19N3O3S/c1-23(20,21)12-14-11-15(19-7-9-22-10-8-19)18-16(17-14)13-5-3-2-4-6-13/h2-6,11H,7-10,12H2,1H3\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],4-(methylsulfonylmethyl)-6-morpholin-4-yl-2-phenylpyrimidine,1.94\nCn1cnc(c2ccccc2)c1c3nc4c(N)ncnc4s3,\"InChI=1S/C15H12N6S/c1-21-8-19-10(9-5-3-2-4-6-9)12(21)15-20-11-13(16)17-7-18-14(11)22-15/h2-8H,1H3,(H2,16,17,18)\",[C][N][C][=N][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Ring1][O][C][=N][C][C][Branch1][C][N][=N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2],\"2-(3-methyl-5-phenylimidazol-4-yl)-[1,3]thiazolo[4,5-e]pyrimidin-7-amine\",2.69\nCCCN(CCO)CCCOc1cc2ncnc(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)c2cc1OC,\"InChI=1S/C28H33F2N7O4/c1-3-8-37(10-11-38)9-5-12-41-24-16-22-19(15-23(24)40-2)28(32-17-31-22)34-25-13-18(35-36-25)14-26(39)33-21-7-4-6-20(29)27(21)30/h4,6-7,13,15-17,38H,3,5,8-12,14H2,1-2H3,(H,33,39)(H2,31,32,34,35,36)\",[C][C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=C][Ring2][Ring1][Branch2][C][=C][Ring2][Ring1][N][O][C],\"n-(2,3-difluorophenyl)-2-[5-[[7-[3-(2-hydroxyethyl-propylamino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\",1.28\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccnc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F,\"InChI=1S/C25H24F3N5O5/c1-15(2)20(21(35)25(26,27)28)32-19(34)13-33-22(17-9-6-10-29-11-17)30-12-18(23(33)36)31-24(37)38-14-16-7-4-3-5-8-16/h3-12,15,20H,13-14H2,1-2H3,(H,31,37)(H,32,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-pyridin-3-ylpyrimidin-5-yl]carbamate\",2.15\nOC(=O)CCn1c2ccccc2c3ccccc13,\"InChI=1S/C15H13NO2/c17-15(18)9-10-16-13-7-3-1-5-11(13)12-6-2-4-8-14(12)16/h1-8H,9-10H2,(H,17,18)\",[O][C][=Branch1][C][=O][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],3-carbazol-9-ylpropanoic acid,0.6\nCSc1ncccc1C(=O)NCCc2ccc(Cl)cc2,\"InChI=1S/C15H15ClN2OS/c1-20-15-13(3-2-9-18-15)14(19)17-10-8-11-4-6-12(16)7-5-11/h2-7,9H,8,10H2,1H3,(H,17,19)\",[C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],n-[2-(4-chlorophenyl)ethyl]-2-methylsulfanylpyridine-3-carboxamide,3.31\nCOc1nc(Cl)cnc1NS(=O)(=O)c2cccc3c(cccc23)N(C)C,\"InChI=1S/C17H17ClN4O3S/c1-22(2)13-8-4-7-12-11(13)6-5-9-14(12)26(23,24)21-16-17(25-3)20-15(18)10-19-16/h4-10H,1-3H3,(H,19,21)\",[C][O][C][=N][C][Branch1][C][Cl][=C][N][=C][Ring1][#Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][Branch1][C][C][C],n-(5-chloro-3-methoxypyrazin-2-yl)-5-dimethylaminonaphthalene-1-sulfonamide,1.74\nC[C@H](CO)Nc1nc(SCc2cccc(Cl)c2F)nc3NC(=O)Sc13,\"InChI=1S/C15H14ClFN4O2S2/c1-7(5-22)18-12-11-13(21-15(23)25-11)20-14(19-12)24-6-8-3-2-4-9(16)10(8)17/h2-4,7,22H,5-6H2,1H3,(H2,18,19,20,21,23)/t7-/m1/s1\",[C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1],\"5-[(3-chloro-2-fluorophenyl)methylsulfanyl]-7-[[(2r)-1-hydroxypropan-2-yl]amino]-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\",3.53\nC1CC(CCN1)c2ccccc2,\"InChI=1S/C11H15N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-5,11-12H,6-9H2\",[C][C][C][Branch1][=Branch1][C][C][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],4-phenylpiperidine,0.54\nCS(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(CCC(c3ccccc3)c4ccccc4)CC2)cc1,\"InChI=1S/C32H38N2O3S/c1-3-21-34(32(35)25-26-14-16-30(17-15-26)38(2,36)37)29-18-22-33(23-19-29)24-20-31(27-10-6-4-7-11-27)28-12-8-5-9-13-28/h3-17,29,31H,1,18-25H2,2H3\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][=N][C][C][=Branch1][C][=O][N][Branch1][Ring2][C][C][=C][C][C][C][N][Branch2][Ring1][=Branch1][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch1][C][=C][Ring2][Ring2][C],\"n-[1-[3,3-di(phenyl)propyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)-n-prop-2-enylacetamide\",3.1\nCOc1cc2c(Nc3c(Cl)ccc4OCOc34)ncnc2cc1OCCCN5CCCC5,\"InChI=1S/C23H25ClN4O4/c1-29-19-11-15-17(12-20(19)30-10-4-9-28-7-2-3-8-28)25-13-26-23(15)27-21-16(24)5-6-18-22(21)32-14-31-18/h5-6,11-13H,2-4,7-10,14H2,1H3,(H,25,26,27)\",[C][O][C][=C][C][=C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][N][=C][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C][C][C][N][C][C][C][C][Ring1][Branch1],\"n-(5-chloro-1,3-benzodioxol-4-yl)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine\",1.62\nCN(C)CCOc1ccccc1Cc2ccccc2,\"InChI=1S/C17H21NO/c1-18(2)12-13-19-17-11-7-6-10-16(17)14-15-8-4-3-5-9-15/h3-11H,12-14H2,1-2H3\",[C][N][Branch1][C][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n,n-dimethyl-2-[2-(phenylmethyl)phenoxy]ethanamine\",2.53\nCc1nnc(NS(=O)(=O)c2ccc(N)cc2)s1,\"InChI=1S/C9H10N4O2S2/c1-6-11-12-9(16-6)13-17(14,15)8-4-2-7(10)3-5-8/h2-5H,10H2,1H3,(H,12,13)\",[C][C][=N][N][=C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][S][Ring1][S],\"4-amino-n-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide\",-1.33\nONC(=O)[C@@H](Cc1ccc2ccccc2c1)NS(=O)(=O)c3ccc4ccccc4c3,\"InChI=1S/C23H20N2O4S/c26-23(24-27)22(14-16-9-10-17-5-1-3-7-19(17)13-16)25-30(28,29)21-12-11-18-6-2-4-8-20(18)15-21/h1-13,15,22,25,27H,14H2,(H,24,26)/t22-/m1/s1\",[O][N][C][=Branch1][C][=O][C@@H1][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2],(2r)-n-hydroxy-3-naphthalen-2-yl-2-(naphthalen-2-ylsulfonylamino)propanamide,3.23\nCOc1cc(\\C=C/2\\SC(=O)NC2=O)cc(OC)c1O,\"InChI=1S/C12H11NO5S/c1-17-7-3-6(4-8(18-2)10(7)14)5-9-11(15)13-12(16)19-9/h3-5,14H,1-2H3,(H,13,15,16)/b9-5+\",[C][O][C][=C][C][Branch1][=N][\\C][=C][\\S][C][=Branch1][C][=O][N][C][/-Ring1][=Branch1][=O][=C][C][Branch1][Ring1][O][C][=C][Ring1][S][O],\"(5e)-5-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione\",0.74\nClc1ccc(OC2CCN(CC2)C3CCN(CC3)S(=O)(=O)NC(=O)c4ccccc4)cc1Cl,\"InChI=1S/C23H27Cl2N3O4S/c24-21-7-6-20(16-22(21)25)32-19-10-12-27(13-11-19)18-8-14-28(15-9-18)33(30,31)26-23(29)17-4-2-1-3-5-17/h1-7,16,18-19H,8-15H2,(H,26,29)\",[Cl][C][=C][C][=C][Branch2][Ring2][#Branch2][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][#C][Cl],\"n-[4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidin-1-yl]sulfonylbenzamide\",2.14\nOC(=O)c1cc2cc(ccc2n1Cc3ccc(Cl)c(Cl)c3)C(F)(F)F,\"InChI=1S/C17H10Cl2F3NO2/c18-12-3-1-9(5-13(12)19)8-23-14-4-2-11(17(20,21)22)6-10(14)7-15(23)16(24)25/h1-7H,8H2,(H,24,25)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch2][Ring1][Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Branch1][C][F][Branch1][C][F][F],\"1-[(3,4-dichlorophenyl)methyl]-5-(trifluoromethyl)indole-2-carboxylic acid\",3.07\nNc1ncnc2ccccc12,\"InChI=1S/C8H7N3/c9-8-6-3-1-2-4-7(6)10-5-11-8/h1-5H,(H2,9,10,11)\",[N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],quinazolin-4-amine,1.26\nCN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)C(O)c3ccccc3,\"InChI=1S/C16H21NO3/c1-17-12-7-8-13(17)10-14(9-12)20-16(19)15(18)11-5-3-2-4-6-11/h2-6,12-15,18H,7-10H2,1H3/t12-,13+,14+,15?\",[C][N][C@@H1][C][C][C@H1][Ring1][Branch1][C][C@H1][Branch1][Ring2][C][Ring1][#Branch1][O][C][=Branch1][C][=O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"[(1r,5s)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2-hydroxy-2-phenylacetate\",-1.29\nC[C@H](N)COc1c(C)cccc1C,\"InChI=1S/C11H17NO/c1-8-5-4-6-9(2)11(8)13-7-10(3)12/h4-6,10H,7,12H2,1-3H3/t10-/m0/s1\",[C][C@H1][Branch1][C][N][C][O][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C],\"(2s)-1-(2,6-dimethylphenoxy)propan-2-amine\",0.6\nCC(C(=O)O)c1ccc2oc(nc2c1)c3ccc(Cl)cc3,\"InChI=1S/C16H12ClNO3/c1-9(16(19)20)11-4-7-14-13(8-11)18-15(21-14)10-2-5-12(17)6-3-10/h2-9H,1H3,(H,19,20)\",[C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][O][C][=Branch1][Branch2][=N][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"2-[2-(4-chlorophenyl)-1,3-benzoxazol-5-yl]propanoic acid\",1.3\nNc1cccc(C(=O)NCC23CC4CC(CC(C4)C2)C3)c1Cl,\"InChI=1S/C18H23ClN2O/c19-16-14(2-1-3-15(16)20)17(22)21-10-18-7-11-4-12(8-18)6-13(5-11)9-18/h1-3,11-13H,4-10,20H2,(H,21,22)\",[N][C][=C][C][=C][C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][Cl],n-(1-adamantylmethyl)-3-amino-2-chlorobenzamide,3.29\nCC1=C(C(=O)c2ccc(O)cc2O1)c3ccccc3,\"InChI=1S/C16H12O3/c1-10-15(11-5-3-2-4-6-11)16(18)13-8-7-12(17)9-14(13)19-10/h2-9,17H,1H3\",[C][C][=C][Branch2][Ring1][Ring1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],7-hydroxy-2-methyl-3-phenylchromen-4-one,2.95\nCCN(C1CCN(CC[C@@H](c2ccc(F)cc2)c3ccc(cc3)S(=O)(=O)C)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H39FN2O5S2/c1-4-35(32(36)23-24-5-13-29(14-6-24)41(2,37)38)28-17-20-34(21-18-28)22-19-31(25-7-11-27(33)12-8-25)26-9-15-30(16-10-26)42(3,39)40/h5-16,28,31H,4,17-23H2,1-3H3/t31-/m0/s1\",[C][C][N][Branch2][Ring2][#C][C][C][C][N][Branch2][Ring2][Ring1][C][C][C@@H1][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-ethyl-n-[1-[(3s)-3-(4-fluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)acetamide,1.88\nO=C(Nc1ccc(nc1)N2CCOCC2)c3oc(Nc4ccccc4)nn3,\"InChI=1S/C18H18N6O3/c25-16(17-22-23-18(27-17)21-13-4-2-1-3-5-13)20-14-6-7-15(19-12-14)24-8-10-26-11-9-24/h1-7,12H,8-11H2,(H,20,25)(H,21,23)\",[O][=C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][O][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][N][=Ring1][N],\"n-(6-morpholin-4-ylpyridin-3-yl)-5-(phenylamino)-1,3,4-oxadiazole-2-carboxamide\",2.9\nCC1(C)CNC(=O)c2sc(nc2C1)N3CCOCC3,\"InChI=1S/C13H19N3O2S/c1-13(2)7-9-10(11(17)14-8-13)19-12(15-9)16-3-5-18-6-4-16/h3-8H2,1-2H3,(H,14,17)\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][C][S][C][=Branch1][Branch2][=N][C][=Ring1][Branch1][C][Ring1][N][N][C][C][O][C][C][Ring1][=Branch1],\"7,7-dimethyl-2-morpholin-4-yl-6,8-dihydro-5h-[1,3]thiazolo[5,4-c]azepin-4-one\",1.29\nC[C@]12CC[C@H]3[C@@H](CC(=C)C4=CC(=O)C=C[C@]34C)[C@@H]1CCC2=O,\"InChI=1S/C20H24O2/c1-12-10-14-15-4-5-18(22)20(15,3)9-7-16(14)19(2)8-6-13(21)11-17(12)19/h6,8,11,14-16H,1,4-5,7,9-10H2,2-3H3/t14-,15-,16-,19+,20-/m0/s1\",[C][C@][C][C][C@H1][C@@H1][Branch2][Ring1][Ring2][C][C][=Branch1][C][=C][C][=C][C][=Branch1][C][=O][C][=C][C@][Ring1][N][Ring1][#Branch1][C][C@@H1][Ring1][P][C][C][C][Ring2][Ring1][Ring2][=O],\"(8r,9s,10r,13s,14s)-10,13-dimethyl-6-methylidene-7,8,9,11,12,14,15,16-octahydrocyclopenta[a]phenanthrene-3,17-dione\",2.98\nNC(=O)Nc1sc(cc1C(=O)N[C@H]2CCCNC2)c3ccccc3,\"InChI=1S/C17H20N4O2S/c18-17(23)21-16-13(15(22)20-12-7-4-8-19-10-12)9-14(24-16)11-5-2-1-3-6-11/h1-3,5-6,9,12,19H,4,7-8,10H2,(H,20,22)(H3,18,21,23)/t12-/m0/s1\",[N][C][=Branch1][C][=O][N][C][S][C][=Branch2][Ring1][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(carbamoylamino)-5-phenyl-n-[(3s)-piperidin-3-yl]thiophene-3-carboxamide,1.27\nCCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3ccccc3OC,\"InChI=1S/C24H30N2O2/c1-4-26(5-2)24(27)20-12-10-18(11-13-20)23(19-14-16-25-17-15-19)21-8-6-7-9-22(21)28-3/h6-13,25H,4-5,14-17H2,1-3H3\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C],\"n,n-diethyl-4-[(2-methoxyphenyl)-piperidin-4-ylidenemethyl]benzamide\",1\nCOc1c(C)cnc(Cn2cnc3c(Cl)nc(N)nc23)c1C,\"InChI=1S/C14H15ClN6O/c1-7-4-17-9(8(2)11(7)22-3)5-21-6-18-10-12(15)19-14(16)20-13(10)21/h4,6H,5H2,1-3H3,(H2,16,19,20)\",[C][O][C][=C][Branch1][C][C][C][=N][C][Branch2][Ring1][Branch1][C][N][C][=N][C][=C][Branch1][C][Cl][N][=C][Branch1][C][N][N][=C][Ring1][O][Ring1][Branch2][=C][Ring2][Ring1][Ring1][C],\"6-chloro-9-[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]purin-2-amine\",1.67\nCC(C)(C(=O)N)C(=O)NCCCNc1nc(Nc2cccc(NC(=O)N3CCCC3)c2)ncc1Br,\"InChI=1S/C23H31BrN8O3/c1-23(2,19(25)33)20(34)27-10-6-9-26-18-17(24)14-28-21(31-18)29-15-7-5-8-16(13-15)30-22(35)32-11-3-4-12-32/h5,7-8,13-14H,3-4,6,9-12H2,1-2H3,(H2,25,33)(H,27,34)(H,30,35)(H2,26,28,29,31)\",[C][C][Branch1][C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][N][C][=N][C][Branch2][Ring1][Branch2][N][C][=C][C][=C][C][Branch1][=N][N][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=C][Ring1][=C][=N][C][=C][Ring2][Ring1][Branch1][Br],\"n'-[3-[[5-bromo-2-[[3-(pyrrolidine-1-carbonylamino)phenyl]amino]pyrimidin-4-yl]amino]propyl]-2,2-dimethylpropanediamide\",2.32\nCC1=CC2=NNC(=O)N2c3cc(ccc13)c4ccncc4,\"InChI=1S/C16H12N4O/c1-10-8-15-18-19-16(21)20(15)14-9-12(2-3-13(10)14)11-4-6-17-7-5-11/h2-9H,1H3,(H,19,21)\",[C][C][=C][C][=N][N][C][=Branch1][C][=O][N][Ring1][=Branch1][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1],\"5-methyl-8-pyridin-4-yl-2h-[1,2,4]triazolo[4,5-a]quinolin-1-one\",2.29\nNc1ncc(NC(=O)c2cc(NC(=O)c3cccc(c3)C(F)(F)F)ccc2Cl)cc1Cl,\"InChI=1S/C20H13Cl2F3N4O2/c21-15-5-4-12(28-18(30)10-2-1-3-11(6-10)20(23,24)25)7-14(15)19(31)29-13-8-16(22)17(26)27-9-13/h1-9H,(H2,26,27)(H,28,30)(H,29,31)\",[N][C][=N][C][=C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][C][=C][Ring2][Ring1][Ring1][Cl][C][=C][Ring2][Ring1][=N][Cl],n-(6-amino-5-chloropyridin-3-yl)-2-chloro-5-[[3-(trifluoromethyl)benzoyl]amino]benzamide,3.26\nCCCCNc1ccc(cc1)C(=O)OCCN(C)C,\"InChI=1S/C15H24N2O2/c1-4-5-10-16-14-8-6-13(7-9-14)15(18)19-12-11-17(2)3/h6-9,16H,4-5,10-12H2,1-3H3\",[C][C][C][C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][N][Branch1][C][C][C],2-dimethylaminoethyl 4-butylaminobenzoate,2.11\nCC(Oc1c(Cl)cccc1Cl)C2=NCCN2,\"InChI=1S/C11H12Cl2N2O/c1-7(11-14-5-6-15-11)16-10-8(12)3-2-4-9(10)13/h2-4,7H,5-6H2,1H3,(H,14,15)\",[C][C][Branch1][=C][O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=N][C][C][N][Ring1][Branch1],\"2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-1h-imidazole\",0.48\nCc1c(Oc2ccc(Cl)cc2)c3c(NS(=O)(=O)C)cccc3n1CC(=O)O,\"InChI=1S/C18H17ClN2O5S/c1-11-18(26-13-8-6-12(19)7-9-13)17-14(20-27(2,24)25)4-3-5-15(17)21(11)10-16(22)23/h3-9,20H,10H2,1-2H3,(H,22,23)\",[C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Ring1][O][N][Ring2][Ring1][=Branch1][C][C][=Branch1][C][=O][O],2-[3-(4-chlorophenoxy)-4-methanesulfonamido-2-methylindol-1-yl]acetic acid,-0.98\nC[C@H](COc1cn2ncnc(Oc3ccc4[nH]c(C)cc4c3F)c2c1C)OC(=O)[C@H](C)N,\"InChI=1S/C22H24FN5O4/c1-11-7-15-16(27-11)5-6-17(19(15)23)32-21-20-13(3)18(8-28(20)26-10-25-21)30-9-12(2)31-22(29)14(4)24/h5-8,10,12,14,27H,9,24H2,1-4H3/t12-,14+/m1/s1\",[C][C@H1][Branch2][Ring2][Branch2][C][O][C][=C][N][N][=C][N][=C][Branch2][Ring1][Ring1][O][C][=C][C][=C][NH1][C][Branch1][C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][F][C][Ring2][Ring1][C][=C][Ring2][Ring1][Branch1][C][O][C][=Branch1][C][=O][C@H1][Branch1][C][C][N],\"[(2r)-1-[4-[(4-fluoro-2-methyl-1h-indol-5-yl)oxy]-5-methylpyrrolo[5,1-f][1,2,4]triazin-6-yl]oxypropan-2-yl] (2s)-2-aminopropanoate\",3.19\nCCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3cccc(c3)C(F)(F)F,\"InChI=1S/C24H27F3N2O/c1-3-29(4-2)23(30)19-10-8-17(9-11-19)22(18-12-14-28-15-13-18)20-6-5-7-21(16-20)24(25,26)27/h5-11,16,28H,3-4,12-15H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"n,n-diethyl-4-[piperidin-4-ylidene-[3-(trifluoromethyl)phenyl]methyl]benzamide\",1.9\nCC[C@H](C)[C@@H](CO)NS(=O)(=O)c1ccc(Cl)s1,\"InChI=1S/C10H16ClNO3S2/c1-3-7(2)8(6-13)12-17(14,15)10-5-4-9(11)16-10/h4-5,7-8,12-13H,3,6H2,1-2H3/t7-,8+/m0/s1\",[C][C][C@H1][Branch1][C][C][C@@H1][Branch1][Ring1][C][O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1],\"5-chloro-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]thiophene-2-sulfonamide\",2.7\nCOCCCOc1ccnc(C[S+]([O-])c2nc3ccccc3[nH]2)c1C,\"InChI=1S/C18H21N3O3S/c1-13-16(19-9-8-17(13)24-11-5-10-23-2)12-25(22)18-20-14-6-3-4-7-15(14)21-18/h3-4,6-9H,5,10-12H2,1-2H3,(H,20,21)\",[C][O][C][C][C][O][C][=C][C][=N][C][Branch2][Ring1][Ring1][C][S+1][Branch1][C][O-1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][=C][Ring2][Ring1][C][C],2-[[4-(3-methoxypropoxy)-3-methylpyridin-2-yl]methylsulfinyl]-1h-benzimidazole,-0.69\nO=C1OC(=Cc2ccccc12)c3ccccc3,InChI=1S/C15H10O2/c16-15-13-9-5-4-8-12(13)10-14(17-15)11-6-2-1-3-7-11/h1-10H,[O][=C][O][C][=Branch1][N][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-phenylisochromen-1-one,3.84\nCC(C)[C@@H]1N(C)c2ccccc2C[C@@H](CO)NC1=O,\"InChI=1S/C15H22N2O2/c1-10(2)14-15(19)16-12(9-18)8-11-6-4-5-7-13(11)17(14)3/h4-7,10,12,14,18H,8-9H2,1-3H3,(H,16,19)/t12-,14-/m0/s1\",[C][C][Branch1][C][C][C@@H1][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C@@H1][Branch1][Ring1][C][O][N][C][Ring1][#C][=O],\"(2s,5s)-5-(hydroxymethyl)-1-methyl-2-propan-2-yl-2,4,5,6-tetrahydro-1,4-benzodiazocin-3-one\",2.03\nCC(=O)NCc1ccc(CN2CCN(CC2)c3ccccc3)cc1,\"InChI=1S/C20H25N3O/c1-17(24)21-15-18-7-9-19(10-8-18)16-22-11-13-23(14-12-22)20-5-3-2-4-6-20/h2-10H,11-16H2,1H3,(H,21,24)\",[C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch2][Ring1][Ring2][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1],n-[[4-[(4-phenylpiperazin-1-yl)methyl]phenyl]methyl]acetamide,1.78\nCOc1ccc(CN2C(=O)NC3=C(C=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C3=O)c4ccccc4)C2=O)cc1,\"InChI=1S/C29H27F3N4O6/c1-16(2)23(25(38)29(30,31)32)33-22(37)15-35-21(18-7-5-4-6-8-18)13-20-24(27(35)40)34-28(41)36(26(20)39)14-17-9-11-19(42-3)12-10-17/h4-13,16,23H,14-15H2,1-3H3,(H,33,37)(H,34,41)\",[C][O][C][=C][C][=C][Branch2][=Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][Branch2][Ring2][P][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][S][=O][C][=C][Ring2][Ring2][Branch2],\"2-[3-[(4-methoxyphenyl)methyl]-2,4,8-trioxo-6-phenyl-1h-pyrido[3,4-d]pyrimidin-7-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",2.93\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN(C)C,\"InChI=1S/C20H22ClFN4O2/c1-26(2)7-4-8-28-19-10-14-17(11-18(19)27-3)23-12-24-20(14)25-13-5-6-16(22)15(21)9-13/h5-6,9-12H,4,7-8H2,1-3H3,(H,23,24,25)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][C][C][C],n-(3-chloro-4-fluorophenyl)-6-(3-dimethylaminopropoxy)-7-methoxyquinazolin-4-amine,2.9\nCC1=CC(=O)Oc2c(C)c3oc(C)cc3cc12,\"InChI=1S/C14H12O3/c1-7-4-12(15)17-14-9(3)13-10(6-11(7)14)5-8(2)16-13/h4-6H,1-3H3\",[C][C][=C][C][=Branch1][C][=O][O][C][=C][Branch1][C][C][C][O][C][Branch1][C][C][=C][C][=Ring1][=Branch1][C][=C][Ring1][S][Ring1][O],\"2,5,9-trimethylpyrano[5,6-f][1]benzoxol-7-one\",3.47\nCC(C)N1CCC[C@@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1,\"InChI=1S/C20H30Cl2N4O/c1-15(2)26-7-3-4-16(14-26)13-24-8-10-25(11-9-24)20(27)23-17-5-6-18(21)19(22)12-17/h5-6,12,15-16H,3-4,7-11,13-14H2,1-2H3,(H,23,27)/t16-/m0/s1\",[C][C][Branch1][C][C][N][C][C][C][C@@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2],\"n-(3,4-dichlorophenyl)-4-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]piperazine-1-carboxamide\",1.62\nCCOc1cc(CC(=O)N[C@@H](CC(C)C)c2ccccc2N3CCCCC3)ccc1C(=O)O,\"InChI=1S/C27H36N2O4/c1-4-33-25-17-20(12-13-22(25)27(31)32)18-26(30)28-23(16-19(2)3)21-10-6-7-11-24(21)29-14-8-5-9-15-29/h6-7,10-13,17,19,23H,4-5,8-9,14-16,18H2,1-3H3,(H,28,30)(H,31,32)/t23-/m0/s1\",[C][C][O][C][=C][C][Branch2][Ring1][S][C][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][C][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][O][C][=Branch1][C][=O][O],2-ethoxy-4-[2-[[(1s)-3-methyl-1-(2-piperidin-1-ylphenyl)butyl]amino]-2-oxoethyl]benzoic acid,2.31\nCN(C)CCCN1c2ccccc2Sc3ccc(Cl)cc13,\"InChI=1S/C17H19ClN2S/c1-19(2)10-5-11-20-14-6-3-4-7-16(14)21-17-9-8-13(18)12-15(17)20/h3-4,6-9,12H,5,10-11H2,1-2H3\",[C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1],\"3-(2-chlorophenothiazin-10-yl)-n,n-dimethylpropan-1-amine\",3.37\nCOc1cccc(Nc2c(cnc3c(C)cc(cc23)S(=O)(=O)c4cccc(c4)C(=O)N(C)C)C(=O)N)c1,\"InChI=1S/C27H26N4O5S/c1-16-11-21(37(34,35)20-10-5-7-17(12-20)27(33)31(2)3)14-22-24(16)29-15-23(26(28)32)25(22)30-18-8-6-9-19(13-18)36-4/h5-15H,1-4H3,(H2,28,32)(H,29,30)\",[C][O][C][=C][C][=C][C][Branch2][Branch1][#Branch1][N][C][=C][Branch2][Ring2][N][C][=N][C][=C][Branch1][C][C][C][=C][Branch1][#Branch1][C][=C][Ring1][O][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=Branch1][C][=O][N][=C][Ring2][Ring2][Ring1],6-[3-(dimethylcarbamoyl)phenyl]sulfonyl-4-[(3-methoxyphenyl)amino]-8-methylquinoline-3-carboxamide,2.69\nO=C1C=C(N=C2N1C=Cc3ccccc23)N4CCOCC4,\"InChI=1S/C16H15N3O2/c20-15-11-14(18-7-9-21-10-8-18)17-16-13-4-2-1-3-12(13)5-6-19(15)16/h1-6,11H,7-10H2\",[O][=C][C][=C][Branch2][Ring1][C][N][=C][N][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"2-morpholin-4-ylpyrimido[2,3-a]isoquinolin-4-one\",2.78\nO=S(=O)(N1CCOCC1)c2cccc(c2)c3cn4cccnc4n3,\"InChI=1S/C16H16N4O3S/c21-24(22,20-7-9-23-10-8-20)14-4-1-3-13(11-14)15-12-19-6-2-5-17-16(19)18-15/h1-6,11-12H,7-10H2\",[O][=S][=Branch1][C][=O][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][=Branch2],\"2-(3-morpholin-4-ylsulfonylphenyl)imidazo[1,2-a]pyrimidine\",1.3\nClc1ccc(cc1)C(N2CCNCC2)c3ccccc3,\"InChI=1S/C17H19ClN2/c18-16-8-6-15(7-9-16)17(14-4-2-1-3-5-14)20-12-10-19-11-13-20/h1-9,17,19H,10-13H2\",[Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],1-[(4-chlorophenyl)-phenylmethyl]piperazine,1.94\nCN1CCN(CC1)c2ccc3N=CN(C(=O)c3c2)c4cc(ccc4C)C(=O)NC5CCC5,\"InChI=1S/C25H29N5O2/c1-17-6-7-18(24(31)27-19-4-3-5-19)14-23(17)30-16-26-22-9-8-20(15-21(22)25(30)32)29-12-10-28(2)11-13-29/h6-9,14-16,19H,3-5,10-13H2,1-2H3,(H,27,31)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][N][Branch1][O][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Ring2],n-cyclobutyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3-yl]benzamide,2.25\nCC(C)(C)NC(=O)C(N(Cc1occc1)C(=O)c2ccc([nH]2)c3ccccc3)c4ccncc4,\"InChI=1S/C27H28N4O3/c1-27(2,3)30-25(32)24(20-13-15-28-16-14-20)31(18-21-10-7-17-34-21)26(33)23-12-11-22(29-23)19-8-5-4-6-9-19/h4-17,24,29H,18H2,1-3H3,(H,30,32)\",[C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][C][Branch2][Ring1][P][N][Branch1][=Branch2][C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1],n-[2-(tert-butylamino)-2-oxo-1-pyridin-4-ylethyl]-n-(furan-2-ylmethyl)-5-phenyl-1h-pyrrole-2-carboxamide,4.13\nCC(C)CC1(CC=C)C(=O)NC(=O)NC1=O,\"InChI=1S/C11H16N2O3/c1-4-5-11(6-7(2)3)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16)\",[C][C][Branch1][C][C][C][C][Branch1][Ring2][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][O][=O],\"5-(2-methylpropyl)-5-prop-2-enyl-1,3-diazinane-2,4,6-trione\",1.48\nCCOC(=O)C1=COc2ccccc2C1=O,\"InChI=1S/C12H10O4/c1-2-15-12(14)9-7-16-10-6-4-3-5-8(10)11(9)13/h3-7H,2H2,1H3\",[C][C][O][C][=Branch1][C][=O][C][=C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O],ethyl 4-oxochromene-3-carboxylate,1.81\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccc(F)cc34)c2C(=O)N5CC[C@@H](O)C5,\"InChI=1S/C26H27FN4O4S/c1-14(2)12-31-25-22(23(33)29(3)26(31)35)21(24(34)30-9-7-17(32)13-30)20(36-25)10-15-6-8-28-19-5-4-16(27)11-18(15)19/h4-6,8,11,14,17,32H,7,9-10,12-13H2,1-3H3/t17-/m1/s1\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][Ring1][C][C][=C][C][=N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][O][Ring1][#Branch1][=C][Ring1][P][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1],\"6-[(6-fluoroquinolin-4-yl)methyl]-5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[4,5-e]pyrimidine-2,4-dione\",1.95\nC[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)NCCCO)C(F)(F)F,\"InChI=1S/C13H16ClF3N2O5S/c1-12(22,13(15,16)17)11(21)19-10-4-3-8(7-9(10)14)25(23,24)18-5-2-6-20/h3-4,7,18,20,22H,2,5-6H2,1H3,(H,19,21)/t12-/m1/s1\",[C][C@@][Branch1][C][O][Branch2][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][O][C][Branch1][C][F][Branch1][C][F][F],\"(2r)-n-[2-chloro-4-(3-hydroxypropylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",2.1\nCOc1ccc(\\C=C\\2/SC(=S)NC2=O)cc1OC,\"InChI=1S/C12H11NO3S2/c1-15-8-4-3-7(5-9(8)16-2)6-10-11(14)13-12(17)18-10/h3-6H,1-2H3,(H,13,14,17)/b10-6-\",[C][O][C][=C][C][=C][Branch1][=N][\\C][=C][/S][C][=Branch1][C][=S][N][C][\\-Ring1][=Branch1][=O][C][=C][Ring1][=C][O][C],\"(5z)-5-[(3,4-dimethoxyphenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one\n5-[(3,4-dimethoxyphenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one\",1.42\nCOc1cc2ncc(C(=O)N)c(Nc3cc(F)ccc3F)c2cc1OC,\"InChI=1S/C18H15F2N3O3/c1-25-15-6-10-13(7-16(15)26-2)22-8-11(18(21)24)17(10)23-14-5-9(19)3-4-12(14)20/h3-8H,1-2H3,(H2,21,24)(H,22,23)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C],\"4-[(2,5-difluorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",2.9\nCc1cc(C)cc(c1)c2oc(SCC(=O)N3CCN(CC3)C(=O)c4occc4)nn2,\"InChI=1S/C21H22N4O4S/c1-14-10-15(2)12-16(11-14)19-22-23-21(29-19)30-13-18(26)24-5-7-25(8-6-24)20(27)17-4-3-9-28-17/h3-4,9-12H,5-8,13H2,1-2H3\",[C][C][=C][C][Branch1][C][C][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][=N][N][=Ring2][Ring1][=Branch1],\"2-[[5-(3,5-dimethylphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethanone\",3\nCOc1ccc(COc2ccc(Cc3cnc(N)nc3N)cc2OC)cc1,\"InChI=1S/C20H22N4O3/c1-25-16-6-3-13(4-7-16)12-27-17-8-5-14(10-18(17)26-2)9-15-11-23-20(22)24-19(15)21/h3-8,10-11H,9,12H2,1-2H3,(H4,21,22,23,24)\",[C][O][C][=C][C][=C][Branch2][Ring1][N][C][O][C][=C][C][=C][Branch1][=C][C][C][=C][N][=C][Branch1][C][N][N][=C][Ring1][#Branch1][N][C][=C][Ring1][#C][O][C][C][=C][Ring2][Ring1][=Branch2],\"5-[[3-methoxy-4-[(4-methoxyphenyl)methoxy]phenyl]methyl]pyrimidine-2,4-diamine\",2.27\nNS(=O)(=O)c1cc(cc(N2CCCC2)c1Oc3ccccc3)C(=O)O,\"InChI=1S/C17H18N2O5S/c18-25(22,23)15-11-12(17(20)21)10-14(19-8-4-5-9-19)16(15)24-13-6-2-1-3-7-13/h1-3,6-7,10-11H,4-5,8-9H2,(H,20,21)(H2,18,22,23)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch2][Ring1][Branch2][=C][C][Branch1][Branch2][N][C][C][C][C][Ring1][Branch1][=C][Ring1][O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O],4-(phenoxy)-3-pyrrolidin-1-yl-5-sulfamoylbenzoic acid,-0.94\nCc1nccn1CCC(C(=O)N)(c2ccccc2)c3ccccc3,\"InChI=1S/C20H21N3O/c1-16-22-13-15-23(16)14-12-20(19(21)24,17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-11,13,15H,12,14H2,1H3,(H2,21,24)\",[C][C][=N][C][=C][N][Ring1][Branch1][C][C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4-(2-methylimidazol-1-yl)-2,2-di(phenyl)butanamide\",1.79\nCC(C(=O)O)c1cccc(Oc2ccccc2)c1,\"InChI=1S/C15H14O3/c1-11(15(16)17)12-6-5-9-14(10-12)18-13-7-3-2-4-8-13/h2-11H,1H3,(H,16,17)\",[C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N],2-[3-(phenoxy)phenyl]propanoic acid,0.71\nCC(=O)c1noc(C)c1C(=O)Nc2nccs2,\"InChI=1S/C10H9N3O3S/c1-5(14)8-7(6(2)16-13-8)9(15)12-10-11-3-4-17-10/h3-4H,1-2H3,(H,11,12,15)\",[C][C][=Branch1][C][=O][C][=N][O][C][Branch1][C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"3-acetyl-5-methyl-n-(1,3-thiazol-2-yl)-1,2-oxazole-4-carboxamide\",1.94\nO=C(N[C@@H]1CN2CCC1CC2)c3ccc(s3)c4ccccc4,\"InChI=1S/C18H20N2OS/c21-18(19-15-12-20-10-8-13(15)9-11-20)17-7-6-16(22-17)14-4-2-1-3-5-14/h1-7,13,15H,8-12H2,(H,19,21)/t15-/m1/s1\",[O][=C][Branch1][=C][N][C@@H1][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],n-[(8s)-1-azabicyclo[2.2.2]octan-8-yl]-5-phenylthiophene-2-carboxamide,1.77\nCNC(=O)c1ccc(Nc2ncc(F)c(n2)c3cnc(C)n3C(C)C)cc1,\"InChI=1S/C19H21FN6O/c1-11(2)26-12(3)22-10-16(26)17-15(20)9-23-19(25-17)24-14-7-5-13(6-8-14)18(27)21-4/h5-11H,1-4H3,(H,21,27)(H,23,24,25)\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][F][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][#Branch1],4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-methylbenzamide,3\nOc1cc(Cl)cc(Cl)c1,\"InChI=1S/C6H4Cl2O/c7-4-1-5(8)3-6(9)2-4/h1-3,9H\",[O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2],\"3,5-dichlorophenol\",3.58\nCSc1ccc(cc1)c2nc(c3ccc(F)cc3)c([nH]2)c4ccncc4,\"InChI=1S/C21H16FN3S/c1-26-18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)\",[C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][Branch1][N][C][C][=C][C][Branch1][C][F][=C][C][=Ring1][#Branch1][=C][Branch1][Ring2][NH1][Ring1][N][C][C][=C][N][=C][C][=Ring1][=Branch1],4-[5-(4-fluorophenyl)-2-(4-methylsulfanylphenyl)-3h-imidazol-4-yl]pyridine,2.97\nCOc1c(N2C[C@@H]3CCCN[C@@H]3C2)c(F)cc4C(=O)C(=CN(C5CC5)c14)C(=O)O,\"InChI=1S/C21H24FN3O4/c1-29-20-17-13(19(26)14(21(27)28)9-25(17)12-4-5-12)7-15(22)18(20)24-8-11-3-2-6-23-16(11)10-24/h7,9,11-12,16,23H,2-6,8,10H2,1H3,(H,27,28)/t11-,16+/m0/s1\",[C][O][C][=C][Branch1][=C][N][C][C@@H1][C][C][C][N][C@@H1][Ring1][=Branch1][C][Ring1][=Branch2][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=Branch1][S][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring2][Ring1][Branch2][=Ring1][#Branch2][C][=Branch1][C][=O][O],\"7-[(4as,7as)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid\",-0.18\nCC(=O)Nc1ccc(cc1)S(=O)(=O)Nc2ccc(Cc3ccncc3)cc2,\"InChI=1S/C20H19N3O3S/c1-15(24)22-18-6-8-20(9-7-18)27(25,26)23-19-4-2-16(3-5-19)14-17-10-12-21-13-11-17/h2-13,23H,14H2,1H3,(H,22,24)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch2][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring1][=N],n-[4-[[4-(pyridin-4-ylmethyl)phenyl]sulfamoyl]phenyl]acetamide,2.8\nCN(C(=O)C)c1ccccc1,\"InChI=1S/C9H11NO/c1-8(11)10(2)9-6-4-3-5-7-9/h3-7H,1-2H3\",[C][N][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],n-methyl-n-phenylacetamide,1.1\nCOC1=CC=C2C(=CC1=O)[C@H](CCc3cc(OC)c(OC)c(OC)c23)NC(=O)C,\"InChI=1S/C22H25NO6/c1-12(24)23-16-8-6-13-10-19(27-3)21(28-4)22(29-5)20(13)14-7-9-18(26-2)17(25)11-15(14)16/h7,9-11,16H,6,8H2,1-5H3,(H,23,24)/t16-/m0/s1\",[C][O][C][=C][C][=C][C][=Branch1][=Branch1][=C][C][Ring1][#Branch1][=O][C@H1][Branch2][Ring1][#Branch2][C][C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][Ring2][Ring1][N][N][C][=Branch1][C][=O][C],\"n-[(7s)-1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5h-benzo[d]heptalen-7-yl]acetamide\",0.82\nCN1CCCC(CC1)N2N=C(Cc3ccc(Cl)cc3)c4ccccc4C2=O,\"InChI=1S/C22H24ClN3O/c1-25-13-4-5-18(12-14-25)26-22(27)20-7-3-2-6-19(20)21(24-26)15-16-8-10-17(23)11-9-16/h2-3,6-11,18H,4-5,12-15H2,1H3\",[C][N][C][C][C][C][Branch1][Branch1][C][C][Ring1][#Branch1][N][N][=C][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][C][=O],4-[(4-chlorophenyl)methyl]-2-(1-methylazepan-4-yl)phthalazin-1-one,2.46\nO=C(Nc1ccccc1)N2CCOCC2,\"InChI=1S/C11H14N2O2/c14-11(13-6-8-15-9-7-13)12-10-4-2-1-3-5-10/h1-5H,6-9H2,(H,12,14)\",[O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],n-phenylmorpholine-4-carboxamide,1\nCCn1c2ccccc2c3cc(NC(=O)N4CCOCC4)ccc13,\"InChI=1S/C19H21N3O2/c1-2-22-17-6-4-3-5-15(17)16-13-14(7-8-18(16)22)20-19(23)21-9-11-24-12-10-21/h3-8,13H,2,9-12H2,1H3,(H,20,23)\",[C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][=Branch1][Ring1][#C],n-(9-ethylcarbazol-3-yl)morpholine-4-carboxamide,3.2\nCN(C)CC(O)COc1ccc(Nc2nccc(Nc3cc(C)ccc3Cl)n2)cc1,\"InChI=1S/C22H26ClN5O2/c1-15-4-9-19(23)20(12-15)26-21-10-11-24-22(27-21)25-16-5-7-18(8-6-16)30-14-17(29)13-28(2)3/h4-12,17,29H,13-14H2,1-3H3,(H2,24,25,26,27)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][Cl][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1],1-[4-[[4-[(2-chloro-5-methylphenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol,2.6\nCC(=O)Nc1cccc(OCc2cnc(Cl)s2)c1,\"InChI=1S/C12H11ClN2O2S/c1-8(16)15-9-3-2-4-10(5-9)17-7-11-6-14-12(13)18-11/h2-6H,7H2,1H3,(H,15,16)\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][=N][O][C][C][=C][N][=C][Branch1][C][Cl][S][Ring1][=Branch1][=C][Ring1][=C],\"n-[3-[(2-chloro-1,3-thiazol-5-yl)methoxy]phenyl]acetamide\",2.38\nCN1CCC(COc2cc(OC3CCOCC3)c4c(Nc5c(Cl)ccc6OCOc56)ncnc4c2)CC1,\"InChI=1S/C27H31ClN4O5/c1-32-8-4-17(5-9-32)14-34-19-12-21-24(23(13-19)37-18-6-10-33-11-7-18)27(30-15-29-21)31-25-20(28)2-3-22-26(25)36-16-35-22/h2-3,12-13,15,17-18H,4-11,14,16H2,1H3,(H,29,30,31)\",[C][N][C][C][C][Branch2][Ring2][P][C][O][C][=C][C][Branch1][#Branch2][O][C][C][C][O][C][C][Ring1][=Branch1][=C][C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=N][C][=N][C][Ring1][P][=C][Ring2][Ring1][N][C][C][Ring2][Ring2][Ring2],\"n-(5-chloro-1,3-benzodioxol-4-yl)-7-[(1-methylpiperidin-4-yl)methoxy]-5-(oxan-4-yloxy)quinazolin-4-amine\",2.59\nCOc1cc2ncnc(NCc3ccccc3)c2cc1OC,\"InChI=1S/C17H17N3O2/c1-21-15-8-13-14(9-16(15)22-2)19-11-20-17(13)18-10-12-6-4-3-5-7-12/h3-9,11H,10H2,1-2H3,(H,18,19,20)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C][C][=C][Ring2][Ring1][C][O][C],\"6,7-dimethoxy-n-(phenylmethyl)quinazolin-4-amine\",3.29\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CC=CC4,\"InChI=1S/C24H24F3N3O3S/c1-14(2)13-30-22-19(20(31)28(3)23(30)33)18(21(32)29-10-6-7-11-29)17(34-22)12-15-8-4-5-9-16(15)24(25,26)27/h4-9,14H,10-13H2,1-3H3\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][=C][C][Ring1][Branch1],\"5-(2,5-dihydropyrrole-1-carbonyl)-3-methyl-1-(2-methylpropyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\",3.53\nCCN(CC)CCCC(C)Nc1c2ccc(Cl)cc2nc3ccc(OC)cc13,\"InChI=1S/C23H30ClN3O/c1-5-27(6-2)13-7-8-16(3)25-23-19-11-9-17(24)14-22(19)26-21-12-10-18(28-4)15-20(21)23/h9-12,14-16H,5-8,13H2,1-4H3,(H,25,26)\",[C][C][N][Branch1][Ring1][C][C][C][C][C][C][Branch1][C][C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][C][Ring1][#Branch1][=N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][P][Ring1][Branch2],\"n'-(6-chloro-2-methoxyacridin-9-yl)-n,n-diethylpentane-1,4-diamine\",2.17\nCc1ccc(Oc2ccc(OCC(=O)Nc3ccncc3)cc2)cc1,\"InChI=1S/C20H18N2O3/c1-15-2-4-18(5-3-15)25-19-8-6-17(7-9-19)24-14-20(23)22-16-10-12-21-13-11-16/h2-13H,14H2,1H3,(H,21,22,23)\",[C][C][=C][C][=C][Branch2][Ring1][O][O][C][=C][C][=C][Branch1][S][O][C][C][=Branch1][C][=O][N][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring1][P][C][=C][Ring2][Ring1][Branch2],2-[4-(4-methylphenoxy)phenoxy]-n-pyridin-4-ylacetamide,4.3\nCc1ccc(cc1)S(=O)(=O)NC(=O)NN2CCCCCC2,\"InChI=1S/C14H21N3O3S/c1-12-6-8-13(9-7-12)21(19,20)16-14(18)15-17-10-4-2-3-5-11-17/h6-9H,2-5,10-11H2,1H3,(H2,15,16,18)\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][N][C][C][C][C][C][C][Ring1][#Branch1],1-(azepan-1-yl)-3-(4-methylphenyl)sulfonylurea,0.01\nOc1ccc(cc1)C2CC(=O)c3c(O)cc(O)cc3O2,\"InChI=1S/C15H12O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-6,13,16-18H,7H2\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][Branch1][C][O][C][=C][Ring1][Branch2][O][Ring1][=N],\"5,7-dihydroxy-2-(4-hydroxyphenyl)chroman-4-one\",2.6\nNc1c(c(CN2CCOCC2)nn1c3ccc(F)cc3)c4ccccc4,\"InChI=1S/C20H21FN4O/c21-16-6-8-17(9-7-16)25-20(22)19(15-4-2-1-3-5-15)18(23-25)14-24-10-12-26-13-11-24/h1-9H,10-14,22H2\",[N][C][=C][Branch2][Ring1][N][C][Branch1][#Branch2][C][N][C][C][O][C][C][Ring1][=Branch1][=N][N][Ring1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(4-fluorophenyl)-5-(morpholin-4-ylmethyl)-4-phenylpyrazol-3-amine,2.33\nNc1nc2ccc(Cl)cc2c3nc(nn13)c4occc4,\"InChI=1S/C13H8ClN5O/c14-7-3-4-9-8(6-7)12-17-11(10-2-1-5-20-10)18-19(12)13(15)16-9/h1-6H,(H2,15,16)\",[N][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=N][C][=Branch1][#Branch1][=N][N][Ring1][=C][Ring1][Branch1][C][O][C][=C][C][=Ring1][Branch1],\"9-chloro-2-furan-2-yl-[1,2,4]triazolo[1,5-c]quinazolin-5-amine\",3.98\nCOc1ccc2ncc(F)c(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2n1,\"InChI=1S/C24H27FN6O3/c1-33-22-5-3-19-23(30-22)17(18(25)13-27-19)8-11-31-9-6-15(7-10-31)26-12-16-2-4-20-24(28-16)29-21(32)14-34-20/h2-5,13,15,26H,6-12,14H2,1H3,(H,28,29,32)\",[C][O][C][=C][C][=C][N][=C][C][Branch1][C][F][=C][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=N][Ring2][Ring1][S],\"6-[[[1-[2-(3-fluoro-6-methoxy-1,5-naphthyridin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",1.78\nCCN(CC)CCN1C(=O)CN=C(c2ccccc2F)c3cc(Cl)ccc13,\"InChI=1S/C21H23ClFN3O/c1-3-25(4-2)11-12-26-19-10-9-15(22)13-17(19)21(24-14-20(26)27)16-7-5-6-8-18(16)23/h5-10,13H,3-4,11-12,14H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring2][Ring1][#Branch1],\"7-chloro-1-(2-diethylaminoethyl)-5-(2-fluorophenyl)-3h-1,4-benzodiazepin-2-one\",2.38\nCS(=O)(=O)c1ccc(cc1Cl)[C@@H](CC2CCCC2)C(=O)Nc3cnc(cn3)[C@H](O)CO,\"InChI=1S/C21H26ClN3O5S/c1-31(29,30)19-7-6-14(9-16(19)22)15(8-13-4-2-3-5-13)21(28)25-20-11-23-17(10-24-20)18(27)12-26/h6-7,9-11,13,15,18,26-27H,2-5,8,12H2,1H3,(H,24,25,28)/t15-,18-/m1/s1\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][N][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C@H1][Branch1][C][O][C][O],\"(2r)-2-(3-chloro-4-methylsulfonylphenyl)-3-cyclopentyl-n-[5-[(1s)-1,2-dihydroxyethyl]pyrazin-2-yl]propanamide\",2.58\nCCN(C(=O)C)c1cccc2c1c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O,\"InChI=1S/C21H21ClN2O3S/c1-4-23(14(3)25)17-6-5-7-18-20(17)21(13(2)24(18)12-19(26)27)28-16-10-8-15(22)9-11-16/h5-11H,4,12H2,1-3H3,(H,26,27)\",[C][C][N][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O],2-[4-(acetyl-ethylamino)-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid,1.61\nCOc1ccc(COC(=O)N2CCC(CNc3ncccn3)CC2)cc1,\"InChI=1S/C19H24N4O3/c1-25-17-5-3-16(4-6-17)14-26-19(24)23-11-7-15(8-12-23)13-22-18-20-9-2-10-21-18/h2-6,9-10,15H,7-8,11-14H2,1H3,(H,20,21,22)\",[C][O][C][=C][C][=C][Branch2][Ring1][O][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][O][C][N][C][=N][C][=C][C][=N][Ring1][=Branch1][C][C][Ring1][=C][C][=C][Ring2][Ring1][Branch2],(4-methoxyphenyl)methyl 4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate,3.14\nCC[C@H](C)C(=O)O[C@H]1C[C@H](O)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@@H]12,\"InChI=1S/C23H36O7/c1-4-13(2)23(29)30-20-11-17(25)9-15-6-5-14(3)19(22(15)20)8-7-16(24)10-18(26)12-21(27)28/h5-6,9,13-14,16-20,22,24-26H,4,7-8,10-12H2,1-3H3,(H,27,28)/t13-,14-,16+,17+,18+,19-,20-,22-/m0/s1\",[C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@H1][Branch1][C][O][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch2][Ring1][C][C][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][C@@H1][Ring2][Ring1][#Branch1][Ring2][Ring1][C],\"(3r,5r)-7-[(1s,2s,6s,8s,8ar)-6-hydroxy-2-methyl-8-[(2s)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid\",-0.76\nCN(C)C(=O)Nc1ccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)cc1,\"InChI=1S/C21H18ClN5O4/c1-26(2)21(31)23-13-6-3-11(4-7-13)10-27-20(30)16-17(19(29)25-27)24-15-9-12(22)5-8-14(15)18(16)28/h3-9H,10H2,1-2H3,(H,23,31)(H,24,28)(H,25,29)\",[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][=C][Ring2][Ring1][=Branch2],\"3-[4-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]phenyl]-1,1-dimethylurea\",1.1\nCCOc1ccccc1c2ccc3c(c2)C(=O)C(=O)c4ccccc34,\"InChI=1S/C22H16O3/c1-2-25-20-10-6-5-7-15(20)14-11-12-17-16-8-3-4-9-18(16)21(23)22(24)19(17)13-14/h3-13H,2H2,1H3\",[C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"2-(2-ethoxyphenyl)phenanthrene-9,10-dione\",2.67\nCc1cccc(NC(=O)NCC(N2CCOCC2)c3cccnc3)c1,\"InChI=1S/C19H24N4O2/c1-15-4-2-6-17(12-15)22-19(24)21-14-18(16-5-3-7-20-13-16)23-8-10-25-11-9-23/h2-7,12-13,18H,8-11,14H2,1H3,(H2,21,22,24)\",[C][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][N][C][C][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][=C][Ring2][Ring1][Branch2],3-(3-methylphenyl)-1-(2-morpholin-4-yl-2-pyridin-3-ylethyl)urea,2\nCN1CCN(CCCN2c3ccccc3Sc4ccc(Cl)cc24)CC1,\"InChI=1S/C20H24ClN3S/c1-22-11-13-23(14-12-22)9-4-10-24-17-5-2-3-6-19(17)25-20-8-7-16(21)15-18(20)24/h2-3,5-8,15H,4,9-14H2,1H3\",[C][N][C][C][N][Branch2][Ring1][O][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1][C][C][Ring2][Ring1][Branch2],2-chloro-10-[3-(4-methylpiperazin-1-yl)propyl]phenothiazine,3.92\nCN[C@@H](C)C(=O)N[C@@H](C1CCCCC1)C(=O)N2CCC[C@H]2C(=O)N[C@@H](C(c3ccccc3)c4ccccc4)C(=O)OC,\"InChI=1S/C33H44N4O5/c1-22(34-2)30(38)35-28(25-18-11-6-12-19-25)32(40)37-21-13-20-26(37)31(39)36-29(33(41)42-3)27(23-14-7-4-8-15-23)24-16-9-5-10-17-24/h4-5,7-10,14-17,22,25-29,34H,6,11-13,18-21H2,1-3H3,(H,35,38)(H,36,39)/t22-,26-,28-,29-/m0/s1\",[C][N][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C@H1][Ring1][Branch1][C][=Branch1][C][=O][N][C@@H1][Branch2][Ring1][Ring2][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C],\"methyl (2s)-2-[[(2s)-1-[(2s)-2-cyclohexyl-2-[[(2s)-2-methylaminopropanoyl]amino]acetyl]pyrrolidine-2-carbonyl]amino]-3,3-di(phenyl)propanoate\",2.42\nCCCNC(=O)c1nnc2c(cccc2c1N)c3ccccc3,\"InChI=1S/C18H18N4O/c1-2-11-20-18(23)17-15(19)14-10-6-9-13(16(14)21-22-17)12-7-4-3-5-8-12/h3-10H,2,11H2,1H3,(H2,19,21)(H,20,23)\",[C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1],4-amino-8-phenyl-n-propylcinnoline-3-carboxamide,3.8\nCOc1cc(ccc1Cn2ncc3ccc(NC(=O)CC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5,\"InChI=1S/C29H30N4O5S/c1-38-27-16-21(29(35)32-39(36,37)25-9-3-2-4-10-25)11-12-23(27)19-33-26-17-24(14-13-22(26)18-30-33)31-28(34)15-20-7-5-6-8-20/h2-4,9-14,16-18,20H,5-8,15,19H2,1H3,(H,31,34)(H,32,35)\",[C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][N][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],4-[[6-[(2-cyclopentylacetyl)amino]indazol-1-yl]methyl]-3-methoxy-n-phenylsulfonylbenzamide,1.6\nCOc1cc2c(ncnc2cc1OCCCN3CCCCC3)N4CCN(CC4)C(=O)Nc5ccc(OC(C)C)cc5,\"InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38)\",[C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][N][=C][N][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][O][C][C][C][N][C][C][C][C][C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch1][O][C][Branch1][C][C][C][C][=C][Ring1][#Branch2],4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-yl]-n-(4-propan-2-yloxyphenyl)piperazine-1-carboxamide,2.6\nCC1=CC(=O)Nc2sc(C(=O)c3ccc(Br)cc3)c(N)c12,\"InChI=1S/C15H11BrN2O2S/c1-7-6-10(19)18-15-11(7)12(17)14(21-15)13(20)8-2-4-9(16)5-3-8/h2-6H,17H2,1H3,(H,18,19)\",[C][C][=C][C][=Branch1][C][=O][N][C][S][C][Branch1][S][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][=C][Branch1][C][N][C][Ring2][Ring1][Ring2][=Ring1][#C],\"3-amino-2-(4-bromobenzoyl)-4-methyl-7h-thieno[3,2-e]pyridin-6-one\",2.57\nCOC(=O)CCCCCCC(=O)Nc1ccc2c(c1)C(=O)C(=O)c3ccccc23,\"InChI=1S/C23H23NO5/c1-29-21(26)11-5-3-2-4-10-20(25)24-15-12-13-17-16-8-6-7-9-18(16)22(27)23(28)19(17)14-15/h6-9,12-14H,2-5,10-11H2,1H3,(H,24,25)\",[C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"methyl 8-[(9,10-dioxophenanthren-2-yl)amino]-8-oxooctanoate\",2.9\nO=C(OCCN1CCCCC1)c2c[nH]c3ccccc23,\"InChI=1S/C16H20N2O2/c19-16(20-11-10-18-8-4-1-5-9-18)14-12-17-15-7-3-2-6-13(14)15/h2-3,6-7,12,17H,1,4-5,8-11H2\",[O][=C][Branch1][N][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1],2-piperidin-1-ylethyl 1h-indole-3-carboxylate,2\nCO[C@H]1CN(CCCOc2ccc(F)cc2)CC[C@H]1NC(=O)c3cc(Cl)c(N)cc3OC,\"InChI=1S/C23H29ClFN3O4/c1-30-21-13-19(26)18(24)12-17(21)23(29)27-20-8-10-28(14-22(20)31-2)9-3-11-32-16-6-4-15(25)5-7-16/h4-7,12-13,20,22H,3,8-11,14,26H2,1-2H3,(H,27,29)/t20-,22+/m1/s1\",[C][O][C@H1][C][N][Branch1][S][C][C][C][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][C@H1][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][N][C][=C][Ring1][Branch2][O][C],\"4-amino-5-chloro-n-[(3s,4r)-1-[3-(4-fluorophenoxy)propyl]-3-methoxypiperidin-4-yl]-2-methoxybenzamide\",3.56\nCN(C)CC(C)(C)COc1nccc(Nc2cc(NC(=O)c3ccnc(c3)N4CCOCC4)ccc2C)n1,\"InChI=1S/C28H37N7O3/c1-20-6-7-22(31-26(36)21-8-10-29-25(16-21)35-12-14-37-15-13-35)17-23(20)32-24-9-11-30-27(33-24)38-19-28(2,3)18-34(4)5/h6-11,16-17H,12-15,18-19H2,1-5H3,(H,31,36)(H,30,32,33)\",[C][N][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][C][O][C][=N][C][=C][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=N][Ring2][Ring1][=N],\"n-[3-[[2-(3-dimethylamino-2,2-dimethylpropoxy)pyrimidin-4-yl]amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide\",2.2\nCS(=O)(=O)Cc1cc(nc(n1)c2ccc3[nH]ccc3c2)N4CCOCC4,\"InChI=1S/C18H20N4O3S/c1-26(23,24)12-15-11-17(22-6-8-25-9-7-22)21-18(20-15)14-2-3-16-13(10-14)4-5-19-16/h2-5,10-11,19H,6-9,12H2,1H3\",[C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=Branch2][Ring1][Branch1][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1],5-[4-(methylsulfonylmethyl)-6-morpholin-4-ylpyrimidin-2-yl]-1h-indole,2.06\nCc1oc(cc1C(=O)O)c2ccc(Cl)cc2,\"InChI=1S/C12H9ClO3/c1-7-10(12(14)15)6-11(16-7)8-2-4-9(13)5-3-8/h2-6H,1H3,(H,14,15)\",[C][C][O][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],5-(4-chlorophenyl)-2-methylfuran-3-carboxylic acid,1.67\nCOc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC,\"InChI=1S/C14H18N4O3/c1-19-10-5-8(6-11(20-2)12(10)21-3)4-9-7-17-14(16)18-13(9)15/h5-7H,4H2,1-3H3,(H4,15,16,17,18)\",[C][O][C][=C][C][Branch1][=C][C][C][=C][N][=C][Branch1][C][N][N][=C][Ring1][#Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][P][O][C],\"5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-diamine\",0.63\nCc1ccc(CNC(=O)C2CCCN2S(=O)(=O)c3ccc(F)cc3)cc1,\"InChI=1S/C19H21FN2O3S/c1-14-4-6-15(7-5-14)13-21-19(23)18-3-2-12-22(18)26(24,25)17-10-8-16(20)9-11-17/h4-11,18H,2-3,12-13H2,1H3,(H,21,23)\",[C][C][=C][C][=C][Branch2][Ring1][S][C][N][C][=Branch1][C][=O][C][C][C][C][N][Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch2],1-(4-fluorophenyl)sulfonyl-n-[(4-methylphenyl)methyl]pyrrolidine-2-carboxamide,2.9\nOC(=O)COCCN1CCN(CC1)C(c2ccccc2)c3ccc(Cl)cc3,\"InChI=1S/C21H25ClN2O3/c22-19-8-6-18(7-9-19)21(17-4-2-1-3-5-17)24-12-10-23(11-13-24)14-15-27-16-20(25)26/h1-9,21H,10-16H2,(H,25,26)\",[O][C][=Branch1][C][=O][C][O][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[2-[4-[(4-chlorophenyl)-phenylmethyl]piperazin-1-yl]ethoxy]acetic acid,1.27\nNC(=O)c1nnn(c1N)c2ccccc2,\"InChI=1S/C9H9N5O/c10-8-7(9(11)15)12-13-14(8)6-4-2-1-3-5-6/h1-5H,10H2,(H2,11,15)\",[N][C][=Branch1][C][=O][C][N][=N][N][Branch1][Branch1][C][=Ring1][Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],5-amino-1-phenyltriazole-4-carboxamide,0.74\nOC(c1ccccc1)c2cccnc2,\"InChI=1S/C12H11NO/c14-12(10-5-2-1-3-6-10)11-7-4-8-13-9-11/h1-9,12,14H\",[O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],phenyl-pyridin-3-ylmethanol,1.72\nCC(CN1c2ccccc2Sc3ccccc13)N(C)C,\"InChI=1S/C17H20N2S/c1-13(18(2)3)12-19-14-8-4-6-10-16(14)20-17-11-7-5-9-15(17)19/h4-11,13H,12H2,1-3H3\",[C][C][Branch2][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][N][Branch1][C][C][C],\"n,n-dimethyl-1-phenothiazin-10-ylpropan-2-amine\",2.67\nc1ccc2[nH]c(nc2c1)c3cscn3,\"InChI=1S/C10H7N3S/c1-2-4-8-7(3-1)12-10(13-8)9-5-14-6-11-9/h1-6H,(H,12,13)\",[C][=C][C][=C][NH1][C][=Branch1][Branch2][=N][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][S][C][=N][Ring1][Branch1],\"2-(1,3-thiazol-4-yl)-1h-benzimidazole\",2.35\nCOc1ccc2Sc3ccccc3N(C[C@H](C)CN(C)C)c2c1,\"InChI=1S/C19H24N2OS/c1-14(12-20(2)3)13-21-16-7-5-6-8-18(16)23-19-10-9-15(22-4)11-17(19)21/h5-11,14H,12-13H2,1-4H3/t14-/m1/s1\",[C][O][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][N][C][C@H1][Branch1][C][C][C][N][Branch1][C][C][C][C][Ring1][P][=C][Ring2][Ring1][Branch1],\"(2r)-3-(2-methoxyphenothiazin-10-yl)-n,n,2-trimethylpropan-1-amine\",2.99\nCOc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCN(C)C,\"InChI=1S/C19H20ClFN4O2/c1-25(2)6-7-27-18-9-13-16(10-17(18)26-3)22-11-23-19(13)24-12-4-5-15(21)14(20)8-12/h4-5,8-11H,6-7H2,1-3H3,(H,22,23,24)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][Branch1][C][C][C],n-(3-chloro-4-fluorophenyl)-6-(2-dimethylaminoethoxy)-7-methoxyquinazolin-4-amine,3.26\nC[C@@](O)(C(=O)Nc1ccc(cc1Cl)C(=O)N2CCCCC2)C(F)(F)F,\"InChI=1S/C16H18ClF3N2O3/c1-15(25,16(18,19)20)14(24)21-12-6-5-10(9-11(12)17)13(23)22-7-3-2-4-8-22/h5-6,9,25H,2-4,7-8H2,1H3,(H,21,24)/t15-/m1/s1\",[C][C@@][Branch1][C][O][Branch2][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"(2r)-n-[2-chloro-4-(piperidine-1-carbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",2.62\nO=C1O[C@]2(CN3CCC2CC3)CN1c4cccs4,\"InChI=1S/C13H16N2O2S/c16-12-15(11-2-1-7-18-11)9-13(17-12)8-14-5-3-10(13)4-6-14/h1-2,7,10H,3-6,8-9H2/t13-/m1/s1\",[O][=C][O][C@][Branch1][N][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][N][Ring1][N][C][=C][C][=C][S][Ring1][Branch1],\"(5r)-3-thiophen-2-ylspiro[1,3-oxazolidine-5,8'-1-azabicyclo[2.2.2]octane]-2-one\",0.9\nCCN(CCO)CCCOc1cc2ncnc(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)c2cc1OC,\"InChI=1S/C27H31F2N7O4/c1-3-36(9-10-37)8-5-11-40-23-15-21-18(14-22(23)39-2)27(31-16-30-21)33-24-12-17(34-35-24)13-25(38)32-20-7-4-6-19(28)26(20)29/h4,6-7,12,14-16,37H,3,5,8-11,13H2,1-2H3,(H,32,38)(H2,30,31,33,34,35)\",[C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=C][Ring2][Ring1][Branch2][C][=C][Ring2][Ring1][N][O][C],\"n-(2,3-difluorophenyl)-2-[5-[[7-[3-(ethyl-(2-hydroxyethyl)amino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\",1.94\nCC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)Nc2ccccc2)C(F)(F)F,\"InChI=1S/C16H15F3N2O4S/c1-15(23,16(17,18)19)14(22)20-11-7-9-13(10-8-11)26(24,25)21-12-5-3-2-4-6-12/h2-10,21,23H,1H3,(H,20,22)\",[C][C][Branch1][C][O][Branch2][Ring1][S][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"3,3,3-trifluoro-2-hydroxy-2-methyl-n-[4-(phenylsulfamoyl)phenyl]propanamide\",3.07\nCC(C)CN1C(=O)N(C)C(=O)c2c(SCCCO)n(Cc3cccc4ccccc34)cc12,\"InChI=1S/C25H29N3O3S/c1-17(2)14-28-21-16-27(15-19-10-6-9-18-8-4-5-11-20(18)19)24(32-13-7-12-29)22(21)23(30)26(3)25(28)31/h4-6,8-11,16-17,29H,7,12-15H2,1-3H3\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Branch1][=Branch1][S][C][C][C][O][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][N][Ring2][Ring1][Branch1],\"5-(3-hydroxypropylsulfanyl)-3-methyl-1-(2-methylpropyl)-6-(naphthalen-1-ylmethyl)pyrrolo[3,4-e]pyrimidine-2,4-dione\",4.36\nCC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)CN3C(=O)CCC3=O)C(=O)C(F)(F)F,\"InChI=1S/C25H25F3N4O6/c1-14(2)22(23(37)25(26,27)28)30-19(34)12-31-17(15-6-4-3-5-7-15)9-8-16(24(31)38)29-18(33)13-32-20(35)10-11-21(32)36/h3-9,14,22H,10-13H2,1-2H3,(H,29,33)(H,30,34)\",[C][C][Branch1][C][C][C][Branch2][Ring2][=N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][=O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[3-[[2-(2,5-dioxopyrrolidin-1-yl)acetyl]amino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",0.96\nCOc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OCC4CCNCC4,\"InChI=1S/C21H22ClFN4O2/c1-28-19-9-15-18(10-20(19)29-11-13-4-6-24-7-5-13)25-12-26-21(15)27-17-3-2-14(22)8-16(17)23/h2-3,8-10,12-13,24H,4-7,11H2,1H3,(H,25,26,27)\",[C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][C][N][C][C][Ring1][=Branch1],n-(4-chloro-2-fluorophenyl)-6-methoxy-7-(piperidin-4-ylmethoxy)quinazolin-4-amine,1.1\nFC(F)(F)CCS(=O)(=O)Oc1ccc(NC(=O)c2ccc(Cn3ccnn3)c4ccccc24)c(n1)C(=O)NCC5CCOCC5,\"InChI=1S/C29H29F3N6O6S/c30-29(31,32)11-16-45(41,42)44-25-8-7-24(26(36-25)28(40)33-17-19-9-14-43-15-10-19)35-27(39)23-6-5-20(18-38-13-12-34-37-38)21-3-1-2-4-22(21)23/h1-8,12-13,19H,9-11,14-18H2,(H,33,40)(H,35,39)\",[F][C][Branch1][C][F][Branch1][C][F][C][C][S][=Branch1][C][=O][=Branch1][C][=O][O][C][=C][C][=C][Branch2][Ring1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch2][C][N][C][=C][N][=N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1][C][=Branch1][Branch1][=N][Ring2][Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][C][C][O][C][C][Ring1][=Branch1],\"[6-(oxan-4-ylmethylcarbamoyl)-5-[[4-(triazol-1-ylmethyl)naphthalene-1-carbonyl]amino]pyridin-2-yl] 3,3,3-trifluoropropane-1-sulfonate\",4.2\nCC(CC(=O)NCc1ccccc1)C2CCCO2,\"InChI=1S/C15H21NO2/c1-12(14-8-5-9-18-14)10-15(17)16-11-13-6-3-2-4-7-13/h2-4,6-7,12,14H,5,8-11H2,1H3,(H,16,17)\",[C][C][Branch1][S][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][C][O][Ring1][Branch1],3-(oxolan-2-yl)-n-(phenylmethyl)butanamide,2.1\nCNc1cc(nc2c(cc(OC)cc12)N3CCN(C)CC3)C(=O)Nc4ccc(cc4)N5CCOCC5,\"InChI=1S/C27H34N6O3/c1-28-23-18-24(27(34)29-19-4-6-20(7-5-19)32-12-14-36-15-13-32)30-26-22(23)16-21(35-3)17-25(26)33-10-8-31(2)9-11-33/h4-7,16-18H,8-15H2,1-3H3,(H,28,30)(H,29,34)\",[C][N][C][=C][C][=Branch2][Ring1][=N][=N][C][=C][Branch1][=N][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][N][Ring1][Branch2][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],6-methoxy-4-methylamino-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)quinoline-2-carboxamide,2.93\nCCn1c2ccccc2c3cc(NC(=O)CN(C)C)ccc13,\"InChI=1S/C18H21N3O/c1-4-21-16-8-6-5-7-14(16)15-11-13(9-10-17(15)21)19-18(22)12-20(2)3/h5-11H,4,12H2,1-3H3,(H,19,22)\",[C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][N][N][C][=Branch1][C][=O][C][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][Ring2][Ring1][=N],2-dimethylamino-n-(9-ethylcarbazol-3-yl)acetamide,3.2\nOC(=O)COc1ccc(Cl)cc1C2CCCCC2,\"InChI=1S/C14H17ClO3/c15-11-6-7-13(18-9-14(16)17)12(8-11)10-4-2-1-3-5-10/h6-8,10H,1-5,9H2,(H,16,17)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][C][C][C][C][Ring1][=Branch1],2-(4-chloro-2-cyclohexylphenoxy)acetic acid,0.93\nFc1ccc(CC2=NNC(=O)c3ccccc23)cc1C(=O)N4CCCNCC4,\"InChI=1S/C21H21FN4O2/c22-18-7-6-14(12-17(18)21(28)26-10-3-8-23-9-11-26)13-19-15-4-1-2-5-16(15)20(27)25-24-19/h1-2,4-7,12,23H,3,8-11,13H2,(H,25,27)\",[F][C][=C][C][=C][Branch2][Ring1][Ring1][C][C][=N][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][C][C][=Branch1][C][=O][N][C][C][C][N][C][C][Ring1][#Branch1],\"4-[[3-(1,4-diazepane-1-carbonyl)-4-fluorophenyl]methyl]-2h-phthalazin-1-one\",0.1\nO=C1C=C(Nc2ccccc12)c3occc3,\"InChI=1S/C13H9NO2/c15-12-8-11(13-6-3-7-16-13)14-10-5-2-1-4-9(10)12/h1-8H,(H,14,15)\",[O][=C][C][=C][Branch1][N][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][O][C][=C][C][=Ring1][Branch1],2-furan-2-yl-1h-quinolin-4-one,2.21\nc1ccc(cc1)c2ccc3ccccc3n2,InChI=1S/C15H11N/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H,[C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2],2-phenylquinoline,4\nCNS(=O)(=O)NC1=CC=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccccc2,\"InChI=1S/C20H23F3N4O5S/c1-12(2)17(18(29)20(21,22)23)25-16(28)11-27-15(13-7-5-4-6-8-13)10-9-14(19(27)30)26-33(31,32)24-3/h4-10,12,17,24,26H,11H2,1-3H3,(H,25,28)\",[C][N][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-[3-(methylsulfamoylamino)-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.79\nCCCCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)O,\"InChI=1S/C18H24N4O/c1-4-5-10-14-21-15-16(22(14)11-18(2,3)23)12-8-6-7-9-13(12)20-17(15)19/h6-9,23H,4-5,10-11H2,1-3H3,(H2,19,20)\",[C][C][C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][Branch1][C][C][O],\"1-(4-amino-2-butylimidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol\",2.37\nC[C@H](CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)sc13,\"InChI=1S/C15H15F2N5OS2/c1-7(5-23)19-12-11-13(20-14(18)25-11)22-15(21-12)24-6-8-3-2-4-9(16)10(8)17/h2-4,7,23H,5-6H2,1H3,(H3,18,19,20,21,22)/t7-/m1/s1\",[C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1],\"(2r)-2-[[2-amino-5-[(2,3-difluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\",3.29\nNC(=N)c1cc2c(\\C=C\\c3ccc4OCOc4c3)cccc2s1,\"InChI=1S/C18H14N2O2S/c19-18(20)17-9-13-12(2-1-3-16(13)23-17)6-4-11-5-7-14-15(8-11)22-10-21-14/h1-9H,10H2,(H3,19,20)/b6-4+\",[N][C][=Branch1][C][=N][C][=C][C][=C][Branch1][S][\\C][=C][\\C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][Ring1][P][S][Ring2][Ring1][Ring2],\"4-[(e)-2-(1,3-benzodioxol-5-yl)ethenyl]-1-benzothiophene-2-carboximidamide\",2.2\nc1ccc2c(c1)nnn2c3ccncc3,InChI=1S/C11H8N4/c1-2-4-11-10(3-1)13-14-15(11)9-5-7-12-8-6-9/h1-8H,[C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=N][N][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1],1-pyridin-4-ylbenzotriazole,1.69\nO=C(NCc1ccccc1)c2cccnc2Oc3ccccc3,\"InChI=1S/C19H16N2O2/c22-18(21-14-15-8-3-1-4-9-15)17-12-7-13-20-19(17)23-16-10-5-2-6-11-16/h1-13H,14H2,(H,21,22)\",[O][=C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(phenoxy)-n-(phenylmethyl)pyridine-3-carboxamide,3\nCN(C)C(=O)N1CCC(CC1)C(=O)NCc2cccs2,\"InChI=1S/C14H21N3O2S/c1-16(2)14(19)17-7-5-11(6-8-17)13(18)15-10-12-4-3-9-20-12/h3-4,9,11H,5-8,10H2,1-2H3,(H,15,18)\",[C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][S][Ring1][Branch1],\"n,n-dimethyl-n'-(thiophen-2-ylmethyl)piperidine-1,4-dicarboxamide\",1.1\nCC(C)N1C(=O)N(C)C(=O)c2cn(Cc3cccc4ccccc34)cc12,\"InChI=1S/C21H21N3O2/c1-14(2)24-19-13-23(12-18(19)20(25)22(3)21(24)26)11-16-9-6-8-15-7-4-5-10-17(15)16/h4-10,12-14H,11H2,1-3H3\",[C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1][Ring1][S],\"3-methyl-6-(naphthalen-1-ylmethyl)-1-propan-2-ylpyrrolo[3,4-e]pyrimidine-2,4-dione\",3.97\nCOc1ccccc1OCCNCC(O)COc2cccc3[nH]c4ccccc4c23,\"InChI=1S/C24H26N2O4/c1-28-21-10-4-5-11-22(21)29-14-13-25-15-17(27)16-30-23-12-6-9-20-24(23)18-7-2-3-8-19(18)26-20/h2-12,17,25-27H,13-16H2,1H3\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=N][=Ring1][=Branch2],1-(9h-carbazol-4-yloxy)-3-[2-(2-methoxyphenoxy)ethylamino]propan-2-ol,3.27\nCC(C)(C)C(=O)NCc1ccc(NC(=O)N2CCCC(O)(C2)c3ccc(Cl)c(Cl)c3)cc1,\"InChI=1S/C24H29Cl2N3O3/c1-23(2,3)21(30)27-14-16-5-8-18(9-6-16)28-22(31)29-12-4-11-24(32,15-29)17-7-10-19(25)20(26)13-17/h5-10,13,32H,4,11-12,14-15H2,1-3H3,(H,27,30)(H,28,31)\",[C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch2][Ring1][P][N][C][=Branch1][C][=O][N][C][C][C][C][Branch1][C][O][Branch1][Ring2][C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][Ring2][Ring1][Branch2],\"3-(3,4-dichlorophenyl)-n-[4-[(2,2-dimethylpropanoylamino)methyl]phenyl]-3-hydroxypiperidine-1-carboxamide\",3.93\nCC[C@H]1N(C2CCCC2)c3nc(Nc4ccc(cc4OC)C(=O)NC5CCN(C)CC5)ncc3N(C)C1=O,\"InChI=1S/C28H39N7O3/c1-5-22-27(37)34(3)23-17-29-28(32-25(23)35(22)20-8-6-7-9-20)31-21-11-10-18(16-24(21)38-4)26(36)30-19-12-14-33(2)15-13-19/h10-11,16-17,19-20,22H,5-9,12-15H2,1-4H3,(H,30,36)(H,29,31,32)/t22-/m1/s1\",[C][C][C@H1][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=N][C][Branch2][Ring1][=C][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=N][C][=C][Ring2][Ring1][=Branch2][N][Branch1][C][C][C][Ring2][Ring2][Ring1][=O],4-[[(7r)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7h-pteridin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide,3.14\nCCCCn1c(Cc2cc(OC)c(OC)c(OC)c2)nc3c(N)ncnc13,\"InChI=1S/C19H25N5O3/c1-5-6-7-24-15(23-16-18(20)21-11-22-19(16)24)10-12-8-13(25-2)17(27-4)14(9-12)26-3/h8-9,11H,5-7,10H2,1-4H3,(H2,20,21,22)\",[C][C][C][C][N][C][Branch2][Ring1][=Branch1][C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][N][=N][C][=C][Branch1][C][N][N][=C][N][=C][Ring2][Ring1][#Branch1][Ring1][#Branch1],\"9-butyl-8-[(3,4,5-trimethoxyphenyl)methyl]purin-6-amine\",2.39\nCc1c(N)cccc1CN2C=CC(=CC2=O)OCCc3cccs3,\"InChI=1S/C19H20N2O2S/c1-14-15(4-2-6-18(14)20)13-21-9-7-16(12-19(21)22)23-10-8-17-5-3-11-24-17/h2-7,9,11-12H,8,10,13,20H2,1H3\",[C][C][=C][Branch1][C][N][C][=C][C][=C][Ring1][#Branch1][C][N][C][=C][C][=Branch1][=Branch1][=C][C][Ring1][=Branch1][=O][O][C][C][C][=C][C][=C][S][Ring1][Branch1],1-[(3-amino-2-methylphenyl)methyl]-4-(2-thiophen-2-ylethoxy)pyridin-2-one,2.78\nCc1ccc(NC(=O)c2ccnc(c2)N3CCOCC3)cc1Nc4ccnc(Cl)n4,\"InChI=1S/C21H21ClN6O2/c1-14-2-3-16(13-17(14)26-18-5-7-24-21(22)27-18)25-20(29)15-4-6-23-19(12-15)28-8-10-30-11-9-28/h2-7,12-13H,8-11H2,1H3,(H,25,29)(H,24,26,27)\",[C][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1][N][C][=C][C][=N][C][Branch1][C][Cl][=N][Ring1][#Branch1],n-[3-[(2-chloropyrimidin-4-yl)amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide,3.1\nOC(=O)C[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4cc(Cl)ccc4[nH]3,\"InChI=1S/C20H17ClN2O3/c21-13-5-6-16-12(7-13)9-18(22-16)20(26)23-17-8-11-3-1-2-4-14(11)15(17)10-19(24)25/h1-7,9,15,17,22H,8,10H2,(H,23,26)(H,24,25)/t15-,17-/m1/s1\",[O][C][=Branch1][C][=O][C][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],\"2-[(1r,2r)-2-[(5-chloro1h-indole-2-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]acetic acid\",1.79\nCC(C)CC(N(C)C)C1(CCC1)c2ccc(Cl)cc2,\"InChI=1S/C17H26ClN/c1-13(2)12-16(19(3)4)17(10-5-11-17)14-6-8-15(18)9-7-14/h6-9,13,16H,5,10-12H2,1-4H3\",[C][C][Branch1][C][C][C][C][Branch1][=Branch1][N][Branch1][C][C][C][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"1-[1-(4-chlorophenyl)cyclobutyl]-n,n,3-trimethylbutan-1-amine\",3.6\nCCCCC1(CC)C(=O)NC(=O)NC1=O,\"InChI=1S/C10H16N2O3/c1-3-5-6-10(4-2)7(13)11-9(15)12-8(10)14/h3-6H2,1-2H3,(H2,11,12,13,14,15)\",[C][C][C][C][C][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][#Branch2][=O],\"5-butyl-5-ethyl-1,3-diazinane-2,4,6-trione\",1.5\nOC(=O)c1ccc(NC(=O)c2cc(OCc3ccccc3)cc(OCc4ccccc4)c2)nc1,\"InChI=1S/C27H22N2O5/c30-26(29-25-12-11-21(16-28-25)27(31)32)22-13-23(33-17-19-7-3-1-4-8-19)15-24(14-22)34-18-20-9-5-2-6-10-20/h1-16H,17-18H2,(H,31,32)(H,28,29,30)\",[O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][#Branch1][N][C][=Branch1][C][=O][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring2][Ring1][=Branch1][N][=C][Ring2][Ring1][#C],\"6-[[3,5-bis(phenylmethoxy)benzoyl]amino]pyridine-3-carboxylic acid\",2.7\nOCC(CO)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)ccc4[nH]3,\"InChI=1S/C22H22ClN3O4/c23-16-5-6-17-15(7-16)9-18(24-17)21(29)25-19-8-14-3-1-2-4-20(14)26(22(19)30)10-13(11-27)12-28/h1-7,9,13,19,24,27-28H,8,10-12H2,(H,25,29)\",[O][C][C][Branch1][Ring1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2],\"5-chloro-n-[1-[3-hydroxy-2-(hydroxymethyl)propyl]-2-oxo-3,4-dihydroquinolin-3-yl]-1h-indole-2-carboxamide\",3.64\nCCOc1ccc(cc1)c2cnc3CCCn23,\"InChI=1S/C14H16N2O/c1-2-17-12-7-5-11(6-8-12)13-10-15-14-4-3-9-16(13)14/h5-8,10H,2-4,9H2,1H3\",[C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][C][C][C][N][Ring1][Branch2][Ring1][Branch1],\"3-(4-ethoxyphenyl)-6,7-dihydro-5h-pyrrolo[1,2-a]imidazole\",2.65\nCNC1=CN=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccc(F)cc2,\"InChI=1S/C19H20F4N4O3/c1-10(2)15(16(29)19(21,22)23)26-14(28)9-27-17(11-4-6-12(20)7-5-11)25-8-13(24-3)18(27)30/h4-8,10,15,24H,9H2,1-3H3,(H,26,28)\",[C][N][C][=C][N][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],\"2-[2-(4-fluorophenyl)-5-methylamino-6-oxopyrimidin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.86\nCN1C(=O)N(C)c2ncn(C)c2C1=O,\"InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3\",[C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][C][C][C][=Ring1][=Branch1][C][Ring1][N][=O],\"1,3,7-trimethylpurine-2,6-dione\",-0.03\nOC1(CNC(=O)c2cc(ccc2Cl)N3N=CC(=O)NC3=O)CCCCCC1,\"InChI=1S/C18H21ClN4O4/c19-14-6-5-12(23-17(26)22-15(24)10-21-23)9-13(14)16(25)20-11-18(27)7-3-1-2-4-8-18/h5-6,9-10,27H,1-4,7-8,11H2,(H,20,25)(H,22,24,26)\",[O][C][Branch2][Ring1][=C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][C][C][C][C][C][Ring2][Ring1][#Branch2],\"2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)-n-[(1-hydroxycycloheptyl)methyl]benzamide\",0.26\nCOc1ccccc1N2CCN(CCN(C(=O)C3CCCCC3)c4ccccn4)CC2,\"InChI=1S/C25H34N4O2/c1-31-23-12-6-5-11-22(23)28-18-15-27(16-19-28)17-20-29(24-13-7-8-14-26-24)25(30)21-9-3-2-4-10-21/h5-8,11-14,21H,2-4,9-10,15-20H2,1H3\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch2][Ring1][#Branch2][C][C][N][Branch1][=N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][C][C][Ring2][Ring1][#Branch1],n-[2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl]-n-pyridin-2-ylcyclohexanecarboxamide,3\nFc1ccccc1NC(=O)N[C@H]2N=C(c3ccccc3)c4ccccc4NC2=O,\"InChI=1S/C22H17FN4O2/c23-16-11-5-7-13-18(16)25-22(29)27-20-21(28)24-17-12-6-4-10-15(17)19(26-20)14-8-2-1-3-9-14/h1-13,20H,(H,24,28)(H2,25,27,29)/t20-/m1/s1\",[F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C@H1][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring1][P][=O],\"3-(2-fluorophenyl)-1-[(3s)-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl]urea\",4\nCc1cccc(Br)c1C(=O)N[C@@H](Cc2ccc(NC(=O)c3c(Cl)cccc3Cl)cc2)C(=O)O,\"InChI=1S/C24H19BrCl2N2O4/c1-13-4-2-5-16(25)20(13)22(30)29-19(24(32)33)12-14-8-10-15(11-9-14)28-23(31)21-17(26)6-3-7-18(21)27/h2-11,19H,12H2,1H3,(H,28,31)(H,29,30)(H,32,33)/t19-/m0/s1\",[C][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C@@H1][Branch2][Ring1][=C][C][C][=C][C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=C][Ring1][P][C][=Branch1][C][=O][O],\"(2s)-2-[(2-bromo-6-methylbenzoyl)amino]-3-[4-[(2,6-dichlorobenzoyl)amino]phenyl]propanoic acid\",-0.13\nC[C@H]1C[C@H]2[C@@H]3CC[C@](O)(C(=O)CO)[C@@]3(C)C[C@H](O)[C@@H]2[C@@]4(C)C=CC(=O)C=C14,\"InChI=1S/C22H30O5/c1-12-8-14-15-5-7-22(27,18(26)11-23)21(15,3)10-17(25)19(14)20(2)6-4-13(24)9-16(12)20/h4,6,9,12,14-15,17,19,23,25,27H,5,7-8,10-11H2,1-3H3/t12-,14-,15-,17-,19+,20-,21-,22-/m0/s1\",[C][C@H1][C][C@H1][C@@H1][C][C][C@][Branch1][C][O][Branch1][#Branch1][C][=Branch1][C][=O][C][O][C@@][Ring1][#Branch2][Branch1][C][C][C][C@H1][Branch1][C][O][C@@H1][Ring1][S][C@@][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2],\"(6s,8s,9s,10r,11s,13s,14s,17r)-11,17-dihydroxy-17-(2-hydroxyacetyl)-6,10,13-trimethyl-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-3-one\",2.12\nFc1ccccc1NC(=O)NC2N=C(c3ccccc3)c4ccccc4NC2=O,\"InChI=1S/C22H17FN4O2/c23-16-11-5-7-13-18(16)25-22(29)27-20-21(28)24-17-12-6-4-10-15(17)19(26-20)14-8-2-1-3-9-14/h1-13,20H,(H,24,28)(H2,25,27,29)\",[F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring1][P][=O],\"3-(2-fluorophenyl)-1-(2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl)urea\",3.8\nClc1ccc(Cl)c(c1)S(=O)(=O)Nc2nc(cs2)c3sccc3Cl,\"InChI=1S/C13H7Cl3N2O2S3/c14-7-1-2-8(15)11(5-7)23(19,20)18-13-17-10(6-22-13)12-9(16)3-4-21-12/h1-6H,(H,17,18)\",[Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][S][C][=C][C][=Ring1][Branch1][Cl],\"2,5-dichloro-n-[4-(3-chlorothiophen-2-yl)-1,3-thiazol-2-yl]benzenesulfonamide\",2.11\nCOc1ccc(C)c(NC(=O)CC23CC4CC(CC(C4)C2)C3)c1,\"InChI=1S/C20H27NO2/c1-13-3-4-17(23-2)8-18(13)21-19(22)12-20-9-14-5-15(10-20)7-16(6-14)11-20/h3-4,8,14-16H,5-7,9-12H2,1-2H3,(H,21,22)\",[C][O][C][=C][C][=C][Branch1][C][C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Branch1],2-(1-adamantyl)-n-(5-methoxy-2-methylphenyl)acetamide,3.96\nCCOc1noc2cc(OCCC3CCN(CC3)c4ccc(C)nn4)ccc12,\"InChI=1S/C21H26N4O3/c1-3-26-21-18-6-5-17(14-19(18)28-24-21)27-13-10-16-8-11-25(12-9-16)20-7-4-15(2)22-23-20/h4-7,14,16H,3,8-13H2,1-2H3\",[C][C][O][C][=N][O][C][=C][C][Branch2][Ring1][=Branch2][O][C][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][C][N][=N][Ring1][#Branch1][=C][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=Branch1],\"3-ethoxy-6-[2-[1-(6-methylpyridazin-3-yl)piperidin-4-yl]ethoxy]-1,2-benzoxazole\",4.23\nCC(C)n1c2ccccc2c3cc(NC(=O)N4CCOCC4)ccc13,\"InChI=1S/C20H23N3O2/c1-14(2)23-18-6-4-3-5-16(18)17-13-15(7-8-19(17)23)21-20(24)22-9-11-25-12-10-22/h3-8,13-14H,9-12H2,1-2H3,(H,21,24)\",[C][C][Branch1][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][=Branch1][Ring1][#C],n-(9-propan-2-ylcarbazol-3-yl)morpholine-4-carboxamide,3.55\nCN1CCN(CC1)C(=O)Cc2csc(NS(=O)(=O)c3cccc(Cl)c3C)n2,\"InChI=1S/C17H21ClN4O3S2/c1-12-14(18)4-3-5-15(12)27(24,25)20-17-19-13(11-26-17)10-16(23)22-8-6-21(2)7-9-22/h3-5,11H,6-10H2,1-2H3,(H,19,20)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][S][C][Branch2][Ring1][Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][Ring1][P],\"3-chloro-2-methyl-n-[4-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-1,3-thiazol-2-yl]benzenesulfonamide\",0.57\nN[C@@H](Cc1c[nH]c2ccccc12)C(=O)O,\"InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m0/s1\",[N][C@@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][O],(2s)-2-amino-3-(1h-indol-3-yl)propanoic acid,-1.08\nNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1,\"InChI=1S/C17H14N6O2S/c18-26(24,25)13-6-4-12(5-7-13)21-17-19-9-8-14(22-17)15-11-20-16-3-1-2-10-23(15)16/h1-11H,(H2,18,24,25)(H,19,21,22)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\",2.7\nC1CN2CCC1C(C2)c3oc(nn3)c4oc(cc4)c5cccnc5,\"InChI=1S/C18H18N4O2/c1-2-13(10-19-7-1)15-3-4-16(23-15)18-21-20-17(24-18)14-11-22-8-5-12(14)6-9-22/h1-4,7,10,12,14H,5-6,8-9,11H2\",[C][C][N][C][C][C][Ring1][=Branch1][C][Branch1][Ring2][C][Ring1][=Branch1][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][O][C][=Branch1][Branch1][=C][C][=Ring1][Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1],\"8-[5-(5-pyridin-3-ylfuran-2-yl)-1,3,4-oxadiazol-2-yl]-1-azabicyclo[2.2.2]octane\",1.2\nCCc1cccc(CC)c1NC(=O)N2Cc3[nH]nc(NC(=O)c4ccc(cc4)N5CCN(C)CC5)c3C2,\"InChI=1S/C28H35N7O2/c1-4-19-7-6-8-20(5-2)25(19)29-28(37)35-17-23-24(18-35)31-32-26(23)30-27(36)21-9-11-22(12-10-21)34-15-13-33(3)14-16-34/h6-12H,4-5,13-18H2,1-3H3,(H,29,37)(H2,30,31,32,36)\",[C][C][C][=C][C][=C][C][Branch1][Ring1][C][C][=C][Ring1][Branch2][N][C][=Branch1][C][=O][N][C][C][NH1][N][=C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Ring2][Ring1][Branch1][C][Ring2][Ring1][Branch2],\"n-(2,6-diethylphenyl)-3-[[4-(4-methylpiperazin-1-yl)benzoyl]amino]-4,6-dihydro-1h-pyrrolo[3,4-d]pyrazole-5-carboxamide\",3.31\nc1ccc(cc1)c2cn3ccccc3n2,InChI=1S/C13H10N2/c1-2-6-11(7-3-1)12-10-15-9-5-4-8-13(15)14-12/h1-10H,[C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2],\"2-phenylimidazo[1,2-a]pyridine\",2.9\nCOC[C@H](O)CN1C(=O)C=NN(C1=O)c2ccc(Cl)c(c2)C(=O)NCC3(O)CCCCCC3,\"InChI=1S/C22H29ClN4O6/c1-33-13-16(28)12-26-19(29)11-25-27(21(26)31)15-6-7-18(23)17(10-15)20(30)24-14-22(32)8-4-2-3-5-9-22/h6-7,10-11,16,28,32H,2-5,8-9,12-14H2,1H3,(H,24,30)/t16-/m1/s1\",[C][O][C][C@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][=N][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][O][C][C][C][C][C][C][Ring1][Branch2],\"2-chloro-n-[(1-hydroxycycloheptyl)methyl]-5-[4-[(2r)-2-hydroxy-3-methoxypropyl]-3,5-dioxo-1,2,4-triazin-2-yl]benzamide\",1.46\nFC(F)(F)c1cc(NC(=O)c2cnc(Cl)nc2C(F)(F)F)cc(c1)C(F)(F)F,\"InChI=1S/C14H5ClF9N3O/c15-11-25-4-8(9(27-11)14(22,23)24)10(28)26-7-2-5(12(16,17)18)1-6(3-7)13(19,20)21/h1-4H,(H,26,28)\",[F][C][Branch1][C][F][Branch1][C][F][C][=C][C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][=C][N][=C][Branch1][C][Cl][N][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][Ring2][C][Branch1][C][F][Branch1][C][F][F],\"n-[3,5-bis(trifluoromethyl)phenyl]-2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxamide\",1.8\nCCC(C)(C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@@H]12,\"InChI=1S/C25H40O6/c1-6-25(4,5)24(30)31-21-12-15(2)11-17-8-7-16(3)20(23(17)21)10-9-18(26)13-19(27)14-22(28)29/h7-8,11,15-16,18-21,23,26-27H,6,9-10,12-14H2,1-5H3,(H,28,29)/t15-,16-,18+,19+,20-,21-,23-/m0/s1\",[C][C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@@H1][Branch1][C][C][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch2][Ring1][C][C][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][C@@H1][Ring2][Ring1][#Branch1][Ring2][Ring1][C],\"(3r,5r)-7-[(1s,2s,6r,8s,8ar)-8-(2,2-dimethylbutanoyloxy)-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid\",1.55\nOc1ccc(cc1)c2sc3cc(O)ccc3c2C(=O)c4ccc(OCCN5CCCCC5)cc4,\"InChI=1S/C28H27NO4S/c30-21-8-4-20(5-9-21)28-26(24-13-10-22(31)18-25(24)34-28)27(32)19-6-11-23(12-7-19)33-17-16-29-14-2-1-3-15-29/h4-13,18,30-31H,1-3,14-17H2\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][S][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][C][=Ring1][#Branch2][C][=Branch1][C][=O][C][=C][C][=C][Branch1][N][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][#C],[6-hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl]-[4-(2-piperidin-1-ylethoxy)phenyl]methanone,4.13\nCCN1CCN(Cc2cnc(c(C)c2)c3ccc(cc3)C(=O)Nc4ccccc4N)CC1,\"InChI=1S/C26H31N5O/c1-3-30-12-14-31(15-13-30)18-20-16-19(2)25(28-17-20)21-8-10-22(11-9-21)26(32)29-24-7-5-4-6-23(24)27/h4-11,16-17H,3,12-15,18,27H2,1-2H3,(H,29,32)\",[C][C][N][C][C][N][Branch2][Ring2][#Branch1][C][C][=C][N][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][Ring2][Ring1][=C],n-(2-aminophenyl)-4-[5-[(4-ethylpiperazin-1-yl)methyl]-3-methylpyridin-2-yl]benzamide,1.2\nCCC(N(CCCN)C(=O)c1ccc(C)cc1)C2=Nc3snc(C)c3C(=O)N2Cc4ccccc4,\"InChI=1S/C27H31N5O2S/c1-4-22(31(16-8-15-28)26(33)21-13-11-18(2)12-14-21)24-29-25-23(19(3)30-35-25)27(34)32(24)17-20-9-6-5-7-10-20/h5-7,9-14,22H,4,8,15-17,28H2,1-3H3\",[C][C][C][Branch2][Ring1][#Branch1][N][Branch1][Branch1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][=N][C][S][N][=C][Branch1][C][C][C][=Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-(3-aminopropyl)-4-methyl-n-[1-[3-methyl-4-oxo-5-(phenylmethyl)-[1,2]thiazolo[5,4-d]pyrimidin-6-yl]propyl]benzamide\",1.61\nCCOC(=O)Cc1csc(NS(=O)(=O)c2ccc(Cl)cc2)n1,\"InChI=1S/C13H13ClN2O4S2/c1-2-20-12(17)7-10-8-21-13(15-10)16-22(18,19)11-5-3-9(14)4-6-11/h3-6,8H,2,7H2,1H3,(H,15,16)\",[C][C][O][C][=Branch1][C][=O][C][C][=C][S][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][S],\"ethyl 2-[2-[(4-chlorophenyl)sulfonylamino]-1,3-thiazol-4-yl]acetate\",1.32\nClc1ccc2Oc3ccccc3N=C(N4CCNCC4)c2c1,\"InChI=1S/C17H16ClN3O/c18-12-5-6-15-13(11-12)17(21-9-7-19-8-10-21)20-14-3-1-2-4-16(14)22-15/h1-6,11,19H,7-10H2\",[Cl][C][=C][C][=C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][Ring1][P][=C][Ring2][Ring1][Branch1],\"8-chloro-6-piperazin-1-ylbenzo[b][1,5]benzoxazepine\",2.28\nCOc1ccc(cc1)c2nc3CCCn3c2Br,\"InChI=1S/C13H13BrN2O/c1-17-10-6-4-9(5-7-10)12-13(14)16-8-2-3-11(16)15-12/h4-7H,2-3,8H2,1H3\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=C][C][C][C][N][Ring1][Branch1][C][=Ring1][Branch2][Br],\"3-bromo-2-(4-methoxyphenyl)-6,7-dihydro-5h-pyrrolo[1,2-a]imidazole\",3.3\nCN1C[C@@H](c2ccccc2)c3cccc(N)c3C1,\"InChI=1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3/t14-/m0/s1\",[C][N][C][C@@H1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1][C][Ring1][P],\"(4s)-2-methyl-4-phenyl-3,4-dihydro-1h-isoquinolin-8-amine\",2.11\nCN([C@H](CN1CCCC1)c2ccccc2)C(=O)Cc3ccc(Cl)c(Cl)c3,\"InChI=1S/C21H24Cl2N2O/c1-24(21(26)14-16-9-10-18(22)19(23)13-16)20(15-25-11-5-6-12-25)17-7-3-2-4-8-17/h2-4,7-10,13,20H,5-6,11-12,14-15H2,1H3/t20-/m1/s1\",[C][N][Branch2][Ring1][Ring2][C@H1][Branch1][=Branch2][C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"2-(3,4-dichlorophenyl)-n-methyl-n-[(1s)-1-phenyl-2-pyrrolidin-1-ylethyl]acetamide\",3.42\nCn1c2ccccc2c3cc(NC(=O)CCc4ccncc4)ccc13,\"InChI=1S/C21H19N3O/c1-24-19-5-3-2-4-17(19)18-14-16(7-8-20(18)24)23-21(25)9-6-15-10-12-22-13-11-15/h2-5,7-8,10-14H,6,9H2,1H3,(H,23,25)\",[C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch2][Ring1][P],n-(9-methylcarbazol-3-yl)-3-pyridin-4-ylpropanamide,3.8\nCC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3Cc4ccncc4C3)c(F)c2,\"InChI=1S/C19H19FN4O3/c1-12(25)22-8-16-11-24(19(26)27-16)15-2-3-18(17(20)6-15)23-9-13-4-5-21-7-14(13)10-23/h2-7,16H,8-11H2,1H3,(H,22,25)/t16-/m0/s1\",[C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][=C][N][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][C][Branch1][C][F][=C][Ring1][S],\"n-[[(5s)-3-[4-(1,3-dihydropyrrolo[3,4-c]pyridin-2-yl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\",3.02\nCc1cc(C)nc(N)c1,\"InChI=1S/C7H10N2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3,(H2,8,9)\",[C][C][=C][C][Branch1][C][C][=N][C][Branch1][C][N][=C][Ring1][Branch2],\"4,6-dimethylpyridin-2-amine\",0.85\nCCCCCCCN(CCc1ccc(OC(C)(C)C(=O)O)cc1)C(=O)Nc2ccc(F)cc2F,\"InChI=1S/C26H34F2N2O4/c1-4-5-6-7-8-16-30(25(33)29-23-14-11-20(27)18-22(23)28)17-15-19-9-12-21(13-10-19)34-26(2,3)24(31)32/h9-14,18H,4-8,15-17H2,1-3H3,(H,29,33)(H,31,32)\",[C][C][C][C][C][C][C][N][Branch2][Ring1][#Branch2][C][C][C][=C][C][=C][Branch1][=C][O][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F],\"2-[4-[2-[(2,4-difluorophenyl)carbamoyl-heptylamino]ethyl]phenoxy]-2-methylpropanoic acid\",1.93\nCN(C)CCNc1cc(nc2cc(nn12)c3ccc(F)cc3)c4ccccc4,\"InChI=1S/C22H22FN5/c1-27(2)13-12-24-21-14-19(16-6-4-3-5-7-16)25-22-15-20(26-28(21)22)17-8-10-18(23)11-9-17/h3-11,14-15,24H,12-13H2,1-2H3\",[C][N][Branch1][C][C][C][C][N][C][=C][C][=Branch2][Ring1][Branch2][=N][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"n-[2-(4-fluorophenyl)-5-phenylpyrazolo[5,1-b]pyrimidin-7-yl]-n',n'-dimethylethane-1,2-diamine\",4.5\nO=S(=O)(Nc1cccnc1)c2ccc3OCCOc3c2,\"InChI=1S/C13H12N2O4S/c16-20(17,15-10-2-1-5-14-9-10)11-3-4-12-13(8-11)19-7-6-18-12/h1-5,8-9,15H,6-7H2\",[O][=S][=Branch1][C][=O][Branch1][#Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][O][C][C][O][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"n-pyridin-3-yl-2,3-dihydro-1,4-benzodioxine-7-sulfonamide\",1.34\nCNCCC(Oc1ccccc1OC)c2ccccc2,\"InChI=1S/C17H21NO2/c1-18-13-12-15(14-8-4-3-5-9-14)20-17-11-7-6-10-16(17)19-2/h3-11,15,18H,12-13H2,1-2H3\",[C][N][C][C][C][Branch1][N][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],3-(2-methoxyphenoxy)-n-methyl-3-phenylpropan-1-amine,0.22\nCC(=O)NCc1ccc(CN2CCN(CC2)c3ccc(F)cc3F)cc1,\"InChI=1S/C20H23F2N3O/c1-15(26)23-13-16-2-4-17(5-3-16)14-24-8-10-25(11-9-24)20-7-6-18(21)12-19(20)22/h2-7,12H,8-11,13-14H2,1H3,(H,23,26)\",[C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch2][Ring1][Branch2][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C][=C][Ring2][Ring1][Branch1],\"n-[[4-[[4-(2,4-difluorophenyl)piperazin-1-yl]methyl]phenyl]methyl]acetamide\",2.5\nClc1ccc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)N5CCNCC5,\"InChI=1S/C22H30ClN3O/c23-20-2-1-18(26-5-3-24-4-6-26)10-19(20)21(27)25-14-22-11-15-7-16(12-22)9-17(8-15)13-22/h1-2,10,15-17,24H,3-9,11-14H2,(H,25,27)\",[Cl][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][C][C][N][C][C][Ring1][=Branch1],n-(1-adamantylmethyl)-2-chloro-5-piperazin-1-ylbenzamide,1.77\nCC[C@H](CO)Nc1nc(NCc2ccccc2)c3ncn(C(C)C)c3n1,\"InChI=1S/C19H26N6O/c1-4-15(11-26)22-19-23-17(20-10-14-8-6-5-7-9-14)16-18(24-19)25(12-21-16)13(2)3/h5-9,12-13,15,26H,4,10-11H2,1-3H3,(H2,20,22,23,24)/t15-/m1/s1\",[C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][N][=C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][Ring1][Branch2][=N][Ring2][Ring1][Ring2],(2r)-2-[[6-(phenylmethylamino)-9-propan-2-ylpurin-2-yl]amino]butan-1-ol,3.63\nNCC(O)(c1ccccc1)c2ccccc2,\"InChI=1S/C14H15NO/c15-11-14(16,12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,16H,11,15H2\",[N][C][C][Branch1][C][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-amino-1,1-di(phenyl)ethanol\",0.9\nCC(Nc1ccccc1)C2=CC(=CN3C(=O)C=C(N=C23)N4CCOCC4)C,\"InChI=1S/C21H24N4O2/c1-15-12-18(16(2)22-17-6-4-3-5-7-17)21-23-19(13-20(26)25(21)14-15)24-8-10-27-11-9-24/h3-7,12-14,16,22H,8-11H2,1-2H3\",[C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch2][Ring1][=Branch2][=C][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][N][=C][Ring1][O][Ring1][#Branch1][N][C][C][O][C][C][Ring1][=Branch1][C],\"7-methyl-2-morpholin-4-yl-9-[1-(phenylamino)ethyl]pyrido[2,1-b]pyrimidin-4-one\",3.6\nNc1ccc2ncnc(Nc3ccc(F)c(Cl)c3)c2c1,\"InChI=1S/C14H10ClFN4/c15-11-6-9(2-3-12(11)16)20-14-10-5-8(17)1-4-13(10)18-7-19-14/h1-7H,17H2,(H,18,19,20)\",[N][C][=C][C][=C][N][=C][N][=C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring1][#C][=C][Ring2][Ring1][Ring1],\"n-(3-chloro-4-fluorophenyl)quinazoline-4,6-diamine\",2.64\nFc1ccc(cc1F)C(=O)Nc2ccc(Cl)nc2,\"InChI=1S/C12H7ClF2N2O/c13-11-4-2-8(6-16-11)17-12(18)7-1-3-9(14)10(15)5-7/h1-6H,(H,17,18)\",[F][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][N][=C][Ring1][#Branch1],\"n-(6-chloropyridin-3-yl)-3,4-difluorobenzamide\",3.31\nCCN(CC)S(=O)(=O)c1ccc(NC(=O)[C@@](C)(O)C(F)(F)F)c(Cl)c1,\"InChI=1S/C14H18ClF3N2O4S/c1-4-20(5-2)25(23,24)9-6-7-11(10(15)8-9)19-12(21)13(3,22)14(16,17)18/h6-8,22H,4-5H2,1-3H3,(H,19,21)/t13-/m1/s1\",[C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C@@][Branch1][C][C][Branch1][C][O][C][Branch1][C][F][Branch1][C][F][F][C][Branch1][C][Cl][=C][Ring1][P],\"(2r)-n-[2-chloro-4-(diethylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",3.66\nCOc1ccc(Nc2ccccc2C(=O)O)cc1,\"InChI=1S/C14H13NO3/c1-18-11-8-6-10(7-9-11)15-13-5-3-2-4-12(13)14(16)17/h2-9,15H,1H3,(H,16,17)\",[C][O][C][=C][C][=C][Branch1][#C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring1][S],2-[(4-methoxyphenyl)amino]benzoic acid,1.2\nc1cnc2cccnc2c1,InChI=1S/C8H6N2/c1-3-7-8(9-5-1)4-2-6-10-7/h1-6H,[C][=C][N][=C][C][=C][C][=N][C][Ring1][=Branch1][=C][Ring1][#Branch2],\"1,5-naphthyridine\",0.89\nNc1nc2ccc(OC(F)(F)F)cc2s1,\"InChI=1S/C8H5F3N2OS/c9-8(10,11)14-4-1-2-5-6(3-4)15-7(12)13-5/h1-3H,(H2,12,13)\",[N][C][=N][C][=C][C][=C][Branch1][#Branch2][O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][O][S][Ring1][=C],\"6-(trifluoromethoxy)-1,3-benzothiazol-2-amine\",3.34\nCN(C)Cc1ccccc1Sc2ccc(C)cc2N,\"InChI=1S/C16H20N2S/c1-12-8-9-16(14(17)10-12)19-15-7-5-4-6-13(15)11-18(2)3/h4-10H,11,17H2,1-3H3\",[C][N][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][N],2-[2-(dimethylaminomethyl)phenyl]sulfanyl-5-methylaniline,2.6\nCOc1ccc2nccc(C(O)C3CC4(CCN3CC4)C=C)c2c1,\"InChI=1S/C20H24N2O2/c1-3-20-7-10-22(11-8-20)18(13-20)19(23)15-6-9-21-17-5-4-14(24-2)12-16(15)17/h3-6,9,12,18-19,23H,1,7-8,10-11,13H2,2H3\",[C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Branch1][C][Branch1][C][O][C][C][C][Branch1][#Branch2][C][C][N][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1],(4-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol,2.08\nCOc1ccc2N=CC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1,\"InChI=1S/C24H29N5O4/c1-31-19-2-3-20-21(13-19)29(24(30)16-27-20)9-8-28-6-4-17(5-7-28)25-14-18-12-22-23(15-26-18)33-11-10-32-22/h2-3,12-13,15-17,25H,4-11,14H2,1H3\",[C][O][C][=C][C][=C][N][=C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C],\"1-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-7-methoxyquinoxalin-2-one\",0.93\nCCN(CC)C(=O)c1ccc(cc1)C(N2CCNCC2)c3cccc4cccnc34,\"InChI=1S/C25H30N4O/c1-3-28(4-2)25(30)21-12-10-20(11-13-21)24(29-17-15-26-16-18-29)22-9-5-7-19-8-6-14-27-23(19)22/h5-14,24,26H,3-4,15-18H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1],\"n,n-diethyl-4-(piperazin-1-yl-quinolin-8-ylmethyl)benzamide\",0.7\nCC1=C2C(=CC(=O)N1Cc3ccccn3)NN(C2=O)c4ccccc4Cl,\"InChI=1S/C19H15ClN4O2/c1-12-18-15(10-17(25)23(12)11-13-6-4-5-9-21-13)22-24(19(18)26)16-8-3-2-7-14(16)20/h2-10,22H,11H2,1H3\",[C][C][=C][C][=Branch2][Ring1][C][=C][C][=Branch1][C][=O][N][Ring1][#Branch1][C][C][=C][C][=C][C][=N][Ring1][=Branch1][N][N][Branch1][Branch1][C][Ring1][S][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],\"2-(2-chlorophenyl)-4-methyl-5-(pyridin-2-ylmethyl)-1h-pyrazolo[5,4-d]pyridine-3,6-dione\",0.2\nCc1ccccc1CN2CCC(CC2)N3CCC(CC3)N4C(=O)Nc5ccccc45,\"InChI=1S/C25H32N4O/c1-19-6-2-3-7-20(19)18-27-14-10-21(11-15-27)28-16-12-22(13-17-28)29-24-9-5-4-8-23(24)26-25(29)30/h2-9,21-22H,10-18H2,1H3,(H,26,30)\",[C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],3-[1-[1-[(2-methylphenyl)methyl]piperidin-4-yl]piperidin-4-yl]-1h-benzimidazol-2-one,2.68\nO=C(CSc1ccccc1)N2CCN(CC2)c3ccccc3,\"InChI=1S/C18H20N2OS/c21-18(15-22-17-9-5-2-6-10-17)20-13-11-19(12-14-20)16-7-3-1-4-8-16/h1-10H,11-15H2\",[O][=C][Branch1][O][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],1-(4-phenylpiperazin-1-yl)-2-phenylsulfanylethanone,3.2\nCCN(CC)CCCNCc1cc(Cl)c2cccnc2c1O,\"InChI=1S/C17H24ClN3O/c1-3-21(4-2)10-6-8-19-12-13-11-15(18)14-7-5-9-20-16(14)17(13)22/h5,7,9,11,19,22H,3-4,6,8,10,12H2,1-2H3\",[C][C][N][Branch1][Ring1][C][C][C][C][C][N][C][C][=C][C][Branch1][C][Cl][=C][C][=C][C][=N][C][Ring1][=Branch1][=C][Ring1][O][O],5-chloro-7-[(3-diethylaminopropylamino)methyl]quinolin-8-ol,0.72\nO[C@@H](CNCCc1ccc(CNCCc2ccccn2)cc1)c3ccc(O)c4NC(=O)Sc34,\"InChI=1S/C25H28N4O3S/c30-21-9-8-20(24-23(21)29-25(32)33-24)22(31)16-27-13-10-17-4-6-18(7-5-17)15-26-14-11-19-3-1-2-12-28-19/h1-9,12,22,26-27,30-31H,10-11,13-16H2,(H,29,32)/t22-/m0/s1\",[O][C@@H1][Branch2][Ring1][O][C][N][C][C][C][=C][C][=C][Branch1][=N][C][N][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[4-[(2-pyridin-2-ylethylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\",-0.25\nClc1ccc2OCOc2c1Nc3ncnc4cc(OCCN5CCCC5)cc(OC6CCOCC6)c34,\"InChI=1S/C26H29ClN4O5/c27-19-3-4-21-25(35-16-34-21)24(19)30-26-23-20(28-15-29-26)13-18(33-12-9-31-7-1-2-8-31)14-22(23)36-17-5-10-32-11-6-17/h3-4,13-15,17H,1-2,5-12,16H2,(H,28,29,30)\",[Cl][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][=N][C][=N][C][=C][C][Branch1][O][O][C][C][N][C][C][C][C][Ring1][Branch1][=C][C][Branch1][#Branch2][O][C][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][Branch1],\"n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine\",2.6\nCCN1C=C(C(=O)O)C(=O)c2ccc(C)nc12,\"InChI=1S/C12H12N2O3/c1-3-14-6-9(12(16)17)10(15)8-5-4-7(2)13-11(8)14/h4-6H,3H2,1-2H3,(H,16,17)\",[C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][N][=C][Ring1][#C][Ring1][#Branch1],\"1-ethyl-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid\",-0.1\nCC(C)[C@H](NC(=O)N(C)Cc1csc(n1)C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc3cncs3)Cc4ccccc4,\"InChI=1S/C37H48N6O5S2/c1-24(2)33(42-36(46)43(5)20-29-22-49-35(40-29)25(3)4)34(45)39-28(16-26-12-8-6-9-13-26)18-32(44)31(17-27-14-10-7-11-15-27)41-37(47)48-21-30-19-38-23-50-30/h6-15,19,22-25,28,31-33,44H,16-18,20-21H2,1-5H3,(H,39,45)(H,41,47)(H,42,46)/t28-,31-,32-,33-/m0/s1\",[C][C][Branch1][C][C][C@H1][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][S][C][=Branch1][Ring2][=N][Ring1][Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C@H1][Branch2][Ring1][S][C][C@H1][Branch1][C][O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][N][=C][S][Ring1][Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1,3-thiazol-5-ylmethyl n-[(2s,3s,5s)-3-hydroxy-5-[[(2s)-3-methyl-2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]butanoyl]amino]-1,6-di(phenyl)hexan-2-yl]carbamate\",4.3\nCSc1ncccc1C(=O)NCC2CCCCC2,\"InChI=1S/C14H20N2OS/c1-18-14-12(8-5-9-15-14)13(17)16-10-11-6-3-2-4-7-11/h5,8-9,11H,2-4,6-7,10H2,1H3,(H,16,17)\",[C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Ring1][=Branch1],n-(cyclohexylmethyl)-2-methylsulfanylpyridine-3-carboxamide,2.93\nCc1c(F)cc(cc1c2ccc(cn2)C(=O)NCC(C)(C)C)C(=O)NC3CC3,\"InChI=1S/C22H26FN3O2/c1-13-17(9-15(10-18(13)23)21(28)26-16-6-7-16)19-8-5-14(11-24-19)20(27)25-12-22(2,3)4/h5,8-11,16H,6-7,12H2,1-4H3,(H,25,27)(H,26,28)\",[C][C][=C][Branch1][C][F][C][=C][Branch2][Ring1][=N][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring1],\"6-[5-(cyclopropylcarbamoyl)-3-fluoro-2-methylphenyl]-n-(2,2-dimethylpropyl)pyridine-3-carboxamide\",3.5\nCN(C)CCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1,\"InChI=1S/C21H23N7O2S/c1-27(2)14-12-24-31(29,30)17-8-6-16(7-9-17)25-21-22-11-10-18(26-21)19-15-23-20-5-3-4-13-28(19)20/h3-11,13,15,24H,12,14H2,1-2H3,(H,22,25,26)\",[C][N][Branch1][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"n-(2-dimethylaminoethyl)-4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\",2.7\nCCN1C2=NC(=O)N(C)C(=O)C2=Cc3ccccc13,\"InChI=1S/C14H13N3O2/c1-3-17-11-7-5-4-6-9(11)8-10-12(17)15-14(19)16(2)13(10)18/h4-8H,3H2,1-2H3\",[C][C][N][C][=N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=Branch2][=C][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1],\"10-ethyl-3-methylpyrimido[6,5-b]quinoline-2,4-dione\",1.1\nCOc1cnc(nc1N2CCOCC2)c3ccccn3,\"InChI=1S/C14H16N4O2/c1-19-12-10-16-13(11-4-2-3-5-15-11)17-14(12)18-6-8-20-9-7-18/h2-5,10H,6-9H2,1H3\",[C][O][C][=C][N][=C][Branch1][=N][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1],5-methoxy-4-morpholin-4-yl-2-pyridin-2-ylpyrimidine,1.52\nNc1nccc(n1)c2cc3C(=O)NC[C@H](CCF)c3[nH]2,\"InChI=1S/C13H14FN5O/c14-3-1-7-6-17-12(20)8-5-10(18-11(7)8)9-2-4-16-13(15)19-9/h2,4-5,7,18H,1,3,6H2,(H,17,20)(H2,15,16,19)/t7-/m0/s1\",[N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][C][=Branch1][C][=O][N][C][C@H1][Branch1][Ring2][C][C][F][C][=Ring1][#Branch2][NH1][Ring1][=N],\"(7s)-2-(2-aminopyrimidin-4-yl)-7-(2-fluoroethyl)-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one\",0.51\nCOC(=O)C1=C(C)NC(=C(C1c2ccccc2[N+](=O)[O-])C(=O)OC)C,\"InChI=1S/C17H18N2O6/c1-9-13(16(20)24-3)15(14(10(2)18-9)17(21)25-4)11-7-5-6-8-12(11)19(22)23/h5-8,15,18H,1-4H3\",[C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][C][=Branch2][Ring1][#Branch2][=C][Branch1][P][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][=Branch1][C][=O][O][C][C],\"dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate\",3.29\nCOc1cccc(c1)[C@@H](C)NCCCc2ccccc2Cl,\"InChI=1S/C18H22ClNO/c1-14(16-8-5-10-17(13-16)21-2)20-12-6-9-15-7-3-4-11-18(15)19/h3-5,7-8,10-11,13-14,20H,6,9,12H2,1-2H3/t14-/m1/s1\",[C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C@@H1][Branch1][C][C][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl],3-(2-chlorophenyl)-n-[(1r)-1-(3-methoxyphenyl)ethyl]propan-1-amine,3\nCOc1cc(cc(OC)c1OC)C(=O)NCc2ccc(OCCN(C)C)cc2,\"InChI=1S/C21H28N2O5/c1-23(2)10-11-28-17-8-6-15(7-9-17)14-22-21(24)16-12-18(25-3)20(27-5)19(13-16)26-4/h6-9,12-13H,10-11,14H2,1-5H3,(H,22,24)\",[C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][=Branch2][O][C][C][N][Branch1][C][C][C][C][=C][Ring1][N],\"n-[[4-(2-dimethylaminoethoxy)phenyl]methyl]-3,4,5-trimethoxybenzamide\",0.74\nCCCNC(=O)c1nnc2c(c(F)ccc2c1N)c3ccc(OC)cc3OC,\"InChI=1S/C20H21FN4O3/c1-4-9-23-20(26)19-17(22)13-7-8-14(21)16(18(13)24-25-19)12-6-5-11(27-2)10-15(12)28-3/h5-8,10H,4,9H2,1-3H3,(H2,22,24)(H,23,26)\",[C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][=C][=C][Branch1][C][F][C][=C][C][Ring1][#Branch1][=C][Ring1][O][N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][O][C],\"4-amino-8-(2,4-dimethoxyphenyl)-7-fluoro-n-propylcinnoline-3-carboxamide\",3.52\nCC(C)OC(=O)N1CCC(CC1)Oc2ncnc3N(CCc23)c4ccc(cc4F)S(=O)(=O)C,\"InChI=1S/C22H27FN4O5S/c1-14(2)31-22(28)26-9-6-15(7-10-26)32-21-17-8-11-27(20(17)24-13-25-21)19-5-4-16(12-18(19)23)33(3,29)30/h4-5,12-15H,6-11H2,1-3H3\",[C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][N][Branch1][Branch2][C][C][C][Ring1][=Branch2][=Ring1][Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C],\"propan-2-yl 4-[[7-(2-fluoro-4-methylsulfonylphenyl)-5,6-dihydropyrrolo[3,2-e]pyrimidin-4-yl]oxy]piperidine-1-carboxylate\",3.4\nCCO\\N=C(\\C1CCN(CC1)C2(C)CCN(CC2)C(=O)c3c(Cl)cncc3Cl)/c4ccc(Br)cc4,\"InChI=1S/C26H31BrCl2N4O2/c1-3-35-31-24(18-4-6-20(27)7-5-18)19-8-12-33(13-9-19)26(2)10-14-32(15-11-26)25(34)23-21(28)16-30-17-22(23)29/h4-7,16-17,19H,3,8-15H2,1-2H3/b31-24+\",[C][C][O][\\N][=C][Branch2][Ring2][Branch2][\\C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=N][C][=C][Ring1][#Branch1][Cl][/C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1],\"[4-[4-[c-(4-bromophenyl)-n-ethoxycarbonimidoyl]piperidin-1-yl]-4-methylpiperidin-1-yl]-(3,5-dichloropyridin-4-yl)methanone\",4\nFC(F)(F)c1cccc(c1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4,\"InChI=1S/C24H26Cl2F3N3O4S/c25-21-5-4-19(15-22(21)26)36-18-8-12-31(13-9-18)17-6-10-32(11-7-17)23(33)30-37(34,35)20-3-1-2-16(14-20)24(27,28)29/h1-5,14-15,17-18H,6-13H2,(H,30,33)\",[F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-[3-(trifluoromethyl)phenyl]sulfonylpiperidine-1-carboxamide\",2.94\nOC(=O)CCC(=O)N1CCC(CC1)c2onc(n2)c3cccs3,\"InChI=1S/C15H17N3O4S/c19-12(3-4-13(20)21)18-7-5-10(6-8-18)15-16-14(17-22-15)11-2-1-9-23-11/h1-2,9-10H,3-8H2,(H,20,21)\",[O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][O][N][=C][Branch1][Ring2][N][=Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1],\"4-oxo-4-[4-(3-thiophen-2-yl-1,2,4-oxadiazol-5-yl)piperidin-1-yl]butanoic acid\",-1.27\nOc1ccc2C(=O)N(C(=O)c2c1)c3ccccc3,\"InChI=1S/C14H9NO3/c16-10-6-7-11-12(8-10)14(18)15(13(11)17)9-4-2-1-3-5-9/h1-8,16H\",[O][C][=C][C][=C][C][=Branch1][C][=O][N][Branch1][O][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-hydroxy-2-phenylisoindole-1,3-dione\",2.3\nCOc1ccc2C=CC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2n1,\"InChI=1S/C24H29N5O4/c1-31-22-4-2-17-3-5-23(30)29(24(17)27-22)11-10-28-8-6-18(7-9-28)25-15-19-14-20-21(16-26-19)33-13-12-32-20/h2-5,14,16,18,25H,6-13,15H2,1H3\",[C][O][C][=C][C][=C][C][=C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=N][Ring2][Ring1][#C],\"1-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-7-methoxy-1,8-naphthyridin-2-one\",1.16\nCc1cc(C)nc(SCC(=O)N)n1,\"InChI=1S/C8H11N3OS/c1-5-3-6(2)11-8(10-5)13-4-7(9)12/h3H,4H2,1-2H3,(H2,9,12)\",[C][C][=C][C][Branch1][C][C][=N][C][Branch1][Branch2][S][C][C][=Branch1][C][=O][N][=N][Ring1][N],\"2-(4,6-dimethylpyrimidin-2-yl)sulfanylacetamide\",0.23\nO[C@@H](CNCCCSCCNCCc1cccc(Cl)c1)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H28ClN3O3S2/c23-16-4-1-3-15(13-16)7-9-24-10-12-30-11-2-8-25-14-19(28)17-5-6-18(27)20-21(17)31-22(29)26-20/h1,3-6,13,19,24-25,27-28H,2,7-12,14H2,(H,26,29)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][#Branch1][C][N][C][C][C][S][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"7-[(1r)-2-[3-[2-[2-(3-chlorophenyl)ethylamino]ethylsulfanyl]propylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",1.06\nCc1ccsc1C(=CCCN2CCC[C@H](C2)C(=O)O)c3sccc3C,\"InChI=1S/C20H25NO2S2/c1-14-7-11-24-18(14)17(19-15(2)8-12-25-19)6-4-10-21-9-3-5-16(13-21)20(22)23/h6-8,11-12,16H,3-5,9-10,13H2,1-2H3,(H,22,23)/t16-/m1/s1\",[C][C][C][=C][S][C][=Ring1][Branch1][C][=Branch2][Ring1][Ring1][=C][C][C][N][C][C][C][C@H1][Branch1][Ring2][C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][S][C][=C][C][=Ring1][Branch1][C],\"(3r)-1-[4,4-bis(3-methylthiophen-2-yl)but-3-enyl]piperidine-3-carboxylic acid\",1.49\nCC1Cc2ccccc2N1NC(=O)c3ccc(Cl)c(c3)S(=O)(=O)N,\"InChI=1S/C16H16ClN3O3S/c1-10-8-11-4-2-3-5-14(11)20(10)19-16(21)12-6-7-13(17)15(9-12)24(18,22)23/h2-7,9-10H,8H2,1H3,(H,19,21)(H2,18,22,23)\",[C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N],\"4-chloro-n-(2-methyl-2,3-dihydroindol-1-yl)-3-sulfamoylbenzamide\",1.83\nC[C@H]1CN(Cc2cc(Cl)ccc2CC(=O)O)CCN1C(=O)Cc3ccc(Cl)cc3,\"InChI=1S/C22H24Cl2N2O3/c1-15-13-25(14-18-11-20(24)7-4-17(18)12-22(28)29)8-9-26(15)21(27)10-16-2-5-19(23)6-3-16/h2-7,11,15H,8-10,12-14H2,1H3,(H,28,29)/t15-/m0/s1\",[C][C@H1][C][N][Branch2][Ring1][Ring1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][C][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[4-chloro-2-[[(3s)-4-[2-(4-chlorophenyl)acetyl]-3-methylpiperazin-1-yl]methyl]phenyl]acetic acid,1.66\nNc1nc(N)c2nc(CO)cnc2n1,\"InChI=1S/C7H8N6O/c8-5-4-6(13-7(9)12-5)10-1-3(2-14)11-4/h1,14H,2H2,(H4,8,9,10,12,13)\",[N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][Ring1][C][O][C][=N][C][Ring1][Branch2][=N][Ring1][=N],\"(2,4-diaminopteridin-6-yl)methanol\",-0.45\nCCOC(=O)Nc1ccc(NCc2ccc(F)cc2)nc1N,\"InChI=1S/C15H17FN4O2/c1-2-22-15(21)19-12-7-8-13(20-14(12)17)18-9-10-3-5-11(16)6-4-10/h3-8H,2,9H2,1H3,(H,19,21)(H3,17,18,20)\",[C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=C][N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][=C][Ring1][#C][N],ethyl n-[2-amino-6-[(4-fluorophenyl)methylamino]pyridin-3-yl]carbamate,2.22\nOC(=O)c1ccccc1NC(=O)Nc2ccccc2,\"InChI=1S/C14H12N2O3/c17-13(18)11-8-4-5-9-12(11)16-14(19)15-10-6-2-1-3-7-10/h1-9H,(H,17,18)(H2,15,16,19)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(phenylcarbamoylamino)benzoic acid,-0.12\nCNC(=O)c1ccc(Nc2nccc(n2)c3cnc(C)n3C(C)C)cc1,\"InChI=1S/C19H22N6O/c1-12(2)25-13(3)22-11-17(25)16-9-10-21-19(24-16)23-15-7-5-14(6-8-15)18(26)20-4/h5-12H,1-4H3,(H,20,26)(H,21,23,24)\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][=Branch1],n-methyl-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide,2.69\nCOC(=O)C1=C(C)NC(=C(C1c2ccccc2[N+](=O)[O-])C(=O)OCC(C)C)C,\"InChI=1S/C20H24N2O6/c1-11(2)10-28-20(24)17-13(4)21-12(3)16(19(23)27-5)18(17)14-8-6-7-9-15(14)22(25)26/h6-9,11,18,21H,10H2,1-5H3\",[C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][C][=Branch2][Ring1][#C][=C][Branch1][P][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][=Branch1][C][=O][O][C][C][Branch1][C][C][C][C],\"o5-methyl o3-(2-methylpropyl) 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate\",3.59\nClc1ccccc1CN2CCc3sccc3C2,\"InChI=1S/C14H14ClNS/c15-13-4-2-1-3-11(13)9-16-7-5-14-12(10-16)6-8-17-14/h1-4,6,8H,5,7,9-10H2\",[Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][C][C][S][C][=C][C][=Ring1][Branch1][C][Ring1][=Branch2],\"5-[(2-chlorophenyl)methyl]-6,7-dihydro-4h-thieno[3,2-c]pyridine\",3.46\nCc1[nH]c2ccccc2c1CCNCc3ccc(\\C=C\\C(=O)NO)cc3,\"InChI=1S/C21H23N3O2/c1-15-18(19-4-2-3-5-20(19)23-15)12-13-22-14-17-8-6-16(7-9-17)10-11-21(25)24-26/h2-11,22-23,26H,12-14H2,1H3,(H,24,25)/b11-10+\",[C][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][N][C][C][=C][C][=C][Branch1][=Branch2][\\C][=C][\\C][=Branch1][C][=O][N][O][C][=C][Ring1][N],(e)-n-hydroxy-3-[4-[[2-(2-methyl-1h-indol-3-yl)ethylamino]methyl]phenyl]prop-2-enamide,1.1\nOCCN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C18H16ClN3O3S/c19-15-9-11-8-12(21-17(11)26-15)16(24)20-13-7-10-3-1-2-4-14(10)22(5-6-23)18(13)25/h1-4,8-9,13,21,23H,5-7H2,(H,20,24)\",[O][C][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-(2-hydroxyethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.05\nOC(=O)c1cncc(c1)c2ccc(Cl)c(c2)C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C24H25ClN2O3/c25-21-2-1-17(18-6-19(23(29)30)12-26-11-18)7-20(21)22(28)27-13-24-8-14-3-15(9-24)5-16(4-14)10-24/h1-2,6-7,11-12,14-16H,3-5,8-10,13H2,(H,27,28)(H,29,30)\",[O][C][=Branch1][C][=O][C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],5-[3-(1-adamantylmethylcarbamoyl)-4-chlorophenyl]pyridine-3-carboxylic acid,0.85\n[O-][N+](=O)c1ccc2c(c1)C(=O)C(=O)c3ccccc23,InChI=1S/C14H7NO4/c16-13-11-4-2-1-3-9(11)10-6-5-8(15(18)19)7-12(10)14(13)17/h1-7H,[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1],\"2-nitrophenanthrene-9,10-dione\",2.42\nCC(C)Nc1ccc2cnn(c3cncc(n3)n4ccc(CC(=O)O)c4)c2c1,\"InChI=1S/C20H20N6O2/c1-13(2)23-16-4-3-15-9-22-26(17(15)8-16)19-11-21-10-18(24-19)25-6-5-14(12-25)7-20(27)28/h3-6,8-13,23H,7H2,1-2H3,(H,27,28)\",[C][C][Branch1][C][C][N][C][=C][C][=C][C][=N][N][Branch2][Ring1][#Branch2][C][=C][N][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][=C][Ring1][=Branch2][C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2],2-[1-[6-[6-(propan-2-ylamino)indazol-1-yl]pyrazin-2-yl]pyrrol-3-yl]acetic acid,1.24\nCOc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN(C)C4(CCN(C)CC4)C(=O)N,\"InChI=1S/C24H28ClFN6O2/c1-31-9-7-24(8-10-31,23(27)33)32(2)13-15-11-16-19(12-20(15)34-3)28-14-29-22(16)30-18-6-4-5-17(25)21(18)26/h4-6,11-12,14H,7-10,13H2,1-3H3,(H2,27,33)(H,28,29,30)\",[C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][Branch1][C][C][C][Branch1][O][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Branch1][C][=O][N],4-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl-methylamino]-1-methylpiperidine-4-carboxamide,2.16\nC[C@@H]1CN[C@@H](C2CC2)C(=O)N(C)[C@H](C)C(=O)N[C@H](Cc3ccc(F)cc3)C(=O)NCCCc4ccccc4O1,\"InChI=1S/C30H39FN4O4/c1-19-18-33-27(23-12-13-23)30(38)35(3)20(2)28(36)34-25(17-21-10-14-24(31)15-11-21)29(37)32-16-6-8-22-7-4-5-9-26(22)39-19/h4-5,7,9-11,14-15,19-20,23,25,27,33H,6,8,12-13,16-18H2,1-3H3,(H,32,37)(H,34,36)/t19-,20-,25-,27+/m1/s1\",[C][C@@H1][C][N][C@@H1][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][Branch1][C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@H1][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][Ring2][Ring2][=Branch1],\"(3r,6s,9r,12r)-6-cyclopropyl-12-[(4-fluorophenyl)methyl]-3,8,9-trimethyl-2-oxa-5,8,11,14-tetrazabicyclo[16.4.0]docosa-1(22),18,20-triene-7,10,13-trione\",3.3\nCc1ccc2cc(C)c3nnc(SCC(=O)N4CCN(CC4)C(=O)c5occc5)n3c2c1,\"InChI=1S/C23H23N5O3S/c1-15-5-6-17-13-16(2)21-24-25-23(28(21)18(17)12-15)32-14-20(29)26-7-9-27(10-8-26)22(30)19-4-3-11-31-19/h3-6,11-13H,7-10,14H2,1-2H3\",[C][C][=C][C][=C][C][=C][Branch1][C][C][C][=N][N][=C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][N][Ring2][Ring1][=Branch1][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C],\"2-[(4,8-dimethyl-[1,2,4]triazolo[4,5-a]quinolin-1-yl)sulfanyl]-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethanone\",2.3\nO=C1C=C(N=C2C=CC=CN12)N3CCOCC3,\"InChI=1S/C12H13N3O2/c16-12-9-11(14-5-7-17-8-6-14)13-10-3-1-2-4-15(10)12/h1-4,9H,5-8H2\",[O][=C][C][=C][Branch1][N][N][=C][C][=C][C][=C][N][Ring1][#Branch2][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"2-morpholin-4-ylpyrido[2,1-b]pyrimidin-4-one\",1\nOc1cc(O)c2C(=O)C(=COc2c1)c3ccc4OCOc4c3,\"InChI=1S/C16H10O6/c17-9-4-11(18)15-14(5-9)20-6-10(16(15)19)8-1-2-12-13(3-8)22-7-21-12/h1-6,17-18H,7H2\",[O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2],\"3-(1,3-benzodioxol-5-yl)-5,7-dihydroxychromen-4-one\",3.5\nN(c1ccccc1)c2ncnc3ccccc23,\"InChI=1S/C14H11N3/c1-2-6-11(7-3-1)17-14-12-8-4-5-9-13(12)15-10-16-14/h1-10H,(H,15,16,17)\",[N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],n-phenylquinazolin-4-amine,2.94\nFC(F)(F)Oc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1,\"InChI=1S/C24H26F3N5O5/c25-24(26,27)37-17-2-4-19-18(11-17)32(22(34)14-36-19)10-9-31-7-5-15(6-8-31)28-12-16-1-3-20-23(29-16)30-21(33)13-35-20/h1-4,11,15,28H,5-10,12-14H2,(H,29,30,33)\",[F][C][Branch1][C][F][Branch1][C][F][O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S],\"6-[[[1-[2-[3-oxo-6-(trifluoromethoxy)-1,4-benzoxazin-4-yl]ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\",1.82\nOC(CCN1CCCC1)(C2CCCCC2)c3ccccc3,\"InChI=1S/C19H29NO/c21-19(17-9-3-1-4-10-17,18-11-5-2-6-12-18)13-16-20-14-7-8-15-20/h1,3-4,9-10,18,21H,2,5-8,11-16H2\",[O][C][Branch1][#Branch2][C][C][N][C][C][C][C][Ring1][Branch1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],1-cyclohexyl-1-phenyl-3-pyrrolidin-1-ylpropan-1-ol,1.78\nC[C@H](NC1=NC(=O)[C@](C)(S1)C(F)(F)F)c2ccccc2F,\"InChI=1S/C13H12F4N2OS/c1-7(8-5-3-4-6-9(8)14)18-11-19-10(20)12(2,21-11)13(15,16)17/h3-7H,1-2H3,(H,18,19,20)/t7-,12-/m0/s1\",[C][C@H1][Branch2][Ring1][=Branch2][N][C][=N][C][=Branch1][C][=O][C@][Branch1][C][C][Branch1][Ring2][S][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F],\"(5s)-2-[[(1s)-1-(2-fluorophenyl)ethyl]amino]-5-methyl-5-(trifluoromethyl)-1,3-thiazol-4-one\",3.1\nFc1ccc(NC(=S)N2CCC(CC2)C(=O)c3ccc(F)cc3)cc1,\"InChI=1S/C19H18F2N2OS/c20-15-3-1-13(2-4-15)18(24)14-9-11-23(12-10-14)19(25)22-17-7-5-16(21)6-8-17/h1-8,14H,9-12H2,(H,22,25)\",[F][C][=C][C][=C][Branch2][Ring1][#C][N][C][=Branch1][C][=S][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][Branch2],4-(4-fluorobenzoyl)-n-(4-fluorophenyl)piperidine-1-carbothioamide,3.4\nBrc1ccc(OC(=O)N2CCN3CCC2CC3)cc1,\"InChI=1S/C14H17BrN2O2/c15-11-1-3-13(4-2-11)19-14(18)17-10-9-16-7-5-12(17)6-8-16/h1-4,12H,5-10H2\",[Br][C][=C][C][=C][Branch2][Ring1][Ring1][O][C][=Branch1][C][=O][N][C][C][N][C][C][C][Ring1][#Branch1][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][C],\"(4-bromophenyl) 1,4-diazabicyclo[3.2.2]nonane-4-carboxylate\",1.58\nCCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cccc(F)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C32H39FN2O5S2/c1-4-35(32(36)22-24-8-12-29(13-9-24)41(2,37)38)28-16-19-34(20-17-28)21-18-31(26-6-5-7-27(33)23-26)25-10-14-30(15-11-25)42(3,39)40/h5-15,23,28,31H,4,16-22H2,1-3H3/t31-/m1/s1\",[C][C][N][Branch2][Ring2][S][C][C][C][N][Branch2][Ring2][Ring2][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],n-ethyl-n-[1-[(3r)-3-(3-fluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)acetamide,2.9\nCOc1cc(OC2CCN(C)CC2)c3c(Nc4cccc5OCOc45)ncnc3c1,\"InChI=1S/C22H24N4O4/c1-26-8-6-14(7-9-26)30-19-11-15(27-2)10-17-20(19)22(24-12-23-17)25-16-4-3-5-18-21(16)29-13-28-18/h3-5,10-12,14H,6-9,13H2,1-2H3,(H,23,24,25)\",[C][O][C][=C][C][Branch1][=N][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][C][Branch1][#C][N][C][=C][C][=C][C][O][C][O][C][Ring1][=Branch2][=Ring1][Branch1][=N][C][=N][C][Ring1][S][=C][Ring2][Ring1][N],\"n-(1,3-benzodioxol-4-yl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine\",3.02\nOC(=O)CCc1ccc(OCc2cccc(Oc3ccccc3)c2)cc1,\"InChI=1S/C22H20O4/c23-22(24)14-11-17-9-12-19(13-10-17)25-16-18-5-4-8-21(15-18)26-20-6-2-1-3-7-20/h1-10,12-13,15H,11,14,16H2,(H,23,24)\",[O][C][=Branch1][C][=O][C][C][C][=C][C][=C][Branch2][Ring1][=Branch1][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][Ring2][Ring1][Branch1],3-[4-[[3-(phenoxy)phenyl]methoxy]phenyl]propanoic acid,2.47\nCOc1cc2c(Nc3ccc(NC(=O)c4ccccc4)cc3)ncnc2cc1OCCCN5CCOCC5,\"InChI=1S/C29H31N5O4/c1-36-26-18-24-25(19-27(26)38-15-5-12-34-13-16-37-17-14-34)30-20-31-28(24)32-22-8-10-23(11-9-22)33-29(35)21-6-3-2-4-7-21/h2-4,6-11,18-20H,5,12-17H2,1H3,(H,33,35)(H,30,31,32)\",[C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#C][N][=C][N][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1],n-[4-[[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-yl]amino]phenyl]benzamide,3.5\nCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4cccnn34)cc1,\"InChI=1S/C17H15N7O2S/c1-18-27(25,26)13-6-4-12(5-7-13)22-17-19-10-8-14(23-17)15-11-20-16-3-2-9-21-24(15)16/h2-11,18H,1H3,(H,19,22,23)\",[C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=N][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1],\"4-[(4-imidazo[2,3-f]pyridazin-3-ylpyrimidin-2-yl)amino]-n-methylbenzenesulfonamide\",2.8\nNC(=O)C1CCN(CC(=O)Nc2ccc3OCOc3c2)CC1,\"InChI=1S/C15H19N3O4/c16-15(20)10-3-5-18(6-4-10)8-14(19)17-11-1-2-12-13(7-11)22-9-21-12/h1-2,7,10H,3-6,8-9H2,(H2,16,20)(H,17,19)\",[N][C][=Branch1][C][=O][C][C][C][N][Branch2][Ring1][Ring2][C][C][=Branch1][C][=O][N][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][C][Ring2][Ring1][Ring1],\"1-[2-(1,3-benzodioxol-5-ylamino)-2-oxoethyl]piperidine-4-carboxamide\",0.4\nCC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccccc2)C(F)(F)F,\"InChI=1S/C16H14F3NO4S/c1-15(22,16(17,18)19)14(21)20-11-7-9-13(10-8-11)25(23,24)12-5-3-2-4-6-12/h2-10,22H,1H3,(H,20,21)\",[C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"3,3,3-trifluoro-2-hydroxy-2-methyl-n-(4-phenylsulfonylphenyl)propanamide\",2.98\nCC(C)(Cc1cccc(CC(=O)NCc2cccc(c2)c3ccc(O)cc3)c1)NC[C@H](O)c4ccc(O)c(NS(=O)(=O)C)c4,\"InChI=1S/C34H39N3O6S/c1-34(2,36-22-32(40)28-12-15-31(39)30(19-28)37-44(3,42)43)20-24-7-4-6-23(16-24)18-33(41)35-21-25-8-5-9-27(17-25)26-10-13-29(38)14-11-26/h4-17,19,32,36-40H,18,20-22H2,1-3H3,(H,35,41)/t32-/m0/s1\",[C][C][Branch1][C][C][Branch2][Ring2][#Branch2][C][C][=C][C][=C][C][Branch2][Ring1][=N][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][Branch2][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Ring1][N],2-[3-[2-[[(2r)-2-hydroxy-2-(4-hydroxy-3-methanesulfonamidophenyl)ethyl]amino]-2-methylpropyl]phenyl]-n-[[3-(4-hydroxyphenyl)phenyl]methyl]acetamide,1.91\nOCCCNc1ccc2c(NC(=O)CC3CCCCC3)c(Cl)ccc2n1,\"InChI=1S/C20H26ClN3O2/c21-16-8-9-17-15(7-10-18(23-17)22-11-4-12-25)20(16)24-19(26)13-14-5-2-1-3-6-14/h7-10,14,25H,1-6,11-13H2,(H,22,23)(H,24,26)\",[O][C][C][C][N][C][=C][C][=C][C][Branch1][#C][N][C][=Branch1][C][=O][C][C][C][C][C][C][C][Ring1][=Branch1][=C][Branch1][C][Cl][C][=C][C][Ring1][P][=N][Ring2][Ring1][Branch1],n-[6-chloro-2-(3-hydroxypropylamino)quinolin-5-yl]-2-cyclohexylacetamide,3.29\nO=C(Nc1ccncc1)c2cccc3ccccc23,\"InChI=1S/C16H12N2O/c19-16(18-13-8-10-17-11-9-13)15-7-3-5-12-4-1-2-6-14(12)15/h1-11H,(H,17,18,19)\",[O][=C][Branch1][#Branch2][N][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],n-pyridin-4-ylnaphthalene-1-carboxamide,3.1\nCC(C)Oc1cc(OCCN2CCN(CC2)C(=O)C)cc3ncnc(Nc4c(F)ccc5OCOc45)c13,\"InChI=1S/C26H30FN5O5/c1-16(2)37-22-13-18(34-11-10-31-6-8-32(9-7-31)17(3)33)12-20-23(22)26(29-14-28-20)30-24-19(27)4-5-21-25(24)36-15-35-21/h4-5,12-14,16H,6-11,15H2,1-3H3,(H,28,29,30)\",[C][C][Branch1][C][C][O][C][=C][C][Branch2][Ring1][Ring1][O][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][F][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=C][Ring2][Ring1][P][Ring1][P],\"1-[4-[2-[4-[(5-fluoro-1,3-benzodioxol-4-yl)amino]-5-propan-2-yloxyquinazolin-7-yl]oxyethyl]piperazin-1-yl]ethanone\",3.06\nNC(=O)Cc1nc(cs1)c2ccccc2,\"InChI=1S/C11H10N2OS/c12-10(14)6-11-13-9(7-15-11)8-4-2-1-3-5-8/h1-5,7H,6H2,(H2,12,14)\",[N][C][=Branch1][C][=O][C][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-(4-phenyl-1,3-thiazol-2-yl)acetamide\",1.3\nCOC(=O)N1CCN(C(CC(=O)NCc2ccc3OCOc3c2)C1)c4ccnc(n4)n5ccnc5,\"InChI=1S/C23H25N7O5/c1-33-23(32)28-8-9-30(20-4-5-25-22(27-20)29-7-6-24-14-29)17(13-28)11-21(31)26-12-16-2-3-18-19(10-16)35-15-34-18/h2-7,10,14,17H,8-9,11-13,15H2,1H3,(H,26,31)\",[C][O][C][=Branch1][C][=O][N][C][C][N][Branch2][Ring1][=N][C][Branch2][Ring1][Branch1][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][Ring2][Ring1][Ring2][C][=C][C][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1],\"methyl 3-[2-(1,3-benzodioxol-5-ylmethylamino)-2-oxoethyl]-4-(2-imidazol-1-ylpyrimidin-4-yl)piperazine-1-carboxylate\",1.88\nC(C1NCCc2ccccc12)c3ccccc3,\"InChI=1S/C16H17N/c1-2-6-13(7-3-1)12-16-15-9-5-4-8-14(15)10-11-17-16/h1-9,16-17H,10-12H2\",[C][Branch1][#C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"1-(phenylmethyl)-1,2,3,4-tetrahydroisoquinoline\",1.89\nCC(C)N1CCC(CC1)N(C(=O)Cc2ccccc2)c3ccc(Cl)cc3,\"InChI=1S/C22H27ClN2O/c1-17(2)24-14-12-21(13-15-24)25(20-10-8-19(23)9-11-20)22(26)16-18-6-4-3-5-7-18/h3-11,17,21H,12-16H2,1-2H3\",[C][C][Branch1][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][Branch1][=C][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],n-(4-chlorophenyl)-2-phenyl-n-(1-propan-2-ylpiperidin-4-yl)acetamide,2.3\nOC(=O)c1cc2cc(ccc2n1Cc3ccc(Cl)c(Cl)c3)[N+](=O)[O-],\"InChI=1S/C16H10Cl2N2O4/c17-12-3-1-9(5-13(12)18)8-19-14-4-2-11(20(23)24)6-10(14)7-15(19)16(21)22/h1-7H,8H2,(H,21,22)\",[O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch2][Ring1][Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][N+1][=Branch1][C][=O][O-1],\"1-[(3,4-dichlorophenyl)methyl]-5-nitroindole-2-carboxylic acid\",1.79\nCCN1CCC[C@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1,\"InChI=1S/C19H28Cl2N4O/c1-2-23-7-3-4-15(13-23)14-24-8-10-25(11-9-24)19(26)22-16-5-6-17(20)18(21)12-16/h5-6,12,15H,2-4,7-11,13-14H2,1H3,(H,22,26)/t15-/m0/s1\",[C][C][N][C][C][C][C@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2],\"n-(3,4-dichlorophenyl)-4-[[(3s)-1-ethylpiperidin-3-yl]methyl]piperazine-1-carboxamide\",1.86\nOC(Cn1cncn1)(Cn2cncn2)c3ccc(F)cc3F,\"InChI=1S/C13H12F2N6O/c14-10-1-2-11(12(15)3-10)13(22,4-20-8-16-6-18-20)5-21-9-17-7-19-21/h1-3,6-9,22H,4-5H2\",[O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F],\"2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazol-1-yl)propan-2-ol\",0.48\nNc1nccc2ccccc12,\"InChI=1S/C9H8N2/c10-9-8-4-2-1-3-7(8)5-6-11-9/h1-6H,(H2,10,11)\",[N][C][=N][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],isoquinolin-1-amine,1.5\nO=C1N2C=CC=CC2=Nc3ccccc13,InChI=1S/C12H8N2O/c15-12-9-5-1-2-6-10(9)13-11-7-3-4-8-14(11)12/h1-8H,[O][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1],\"pyrido[2,1-b]quinazolin-11-one\",2.1\nCOC(=O)c1cccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)c1,\"InChI=1S/C20H14ClN3O5/c1-29-20(28)11-4-2-3-10(7-11)9-24-19(27)15-16(18(26)23-24)22-14-8-12(21)5-6-13(14)17(15)25/h2-8H,9H2,1H3,(H,22,25)(H,23,26)\",[C][O][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][=C][Ring2][Ring1][=Branch2],\"methyl 3-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]benzoate\",1.1\nCCN1CCN(CC1)C(=O)c2cc3ccccc3[nH]2,\"InChI=1S/C15H19N3O/c1-2-17-7-9-18(10-8-17)15(19)14-11-12-5-3-4-6-13(12)16-14/h3-6,11,16H,2,7-10H2,1H3\",[C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],(4-ethylpiperazin-1-yl)-(1h-indol-2-yl)methanone,1.95\nOC(=O)c1[nH]c2ccccc2c1CC(=O)Nc3cccc(c3)C(F)(F)F,\"InChI=1S/C18H13F3N2O3/c19-18(20,21)10-4-3-5-11(8-10)22-15(24)9-13-12-6-1-2-7-14(12)23-16(13)17(25)26/h1-8,23H,9H2,(H,22,24)(H,25,26)\",[O][C][=Branch1][C][=O][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],3-[2-oxo-2-[[3-(trifluoromethyl)phenyl]amino]ethyl]-1h-indole-2-carboxylic acid,1.33\nC[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc3cccc(Cl)c3,\"InChI=1S/C22H24Cl2N2O4/c1-15-12-25(13-17-11-19(24)5-6-20(17)30-14-22(28)29)7-8-26(15)21(27)10-16-3-2-4-18(23)9-16/h2-6,9,11,15H,7-8,10,12-14H2,1H3,(H,28,29)/t15-/m0/s1\",[C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1],2-[4-chloro-2-[[(3s)-4-[2-(3-chlorophenyl)acetyl]-3-methylpiperazin-1-yl]methyl]phenoxy]acetic acid,0.78\nCOc1cccc(OC)c1c2ccc(C[C@H](NC(=O)c3c(Cl)cccc3Cl)C(=O)O)cc2,\"InChI=1S/C24H21Cl2NO5/c1-31-19-7-4-8-20(32-2)21(19)15-11-9-14(10-12-15)13-18(24(29)30)27-23(28)22-16(25)5-3-6-17(22)26/h3-12,18H,13H2,1-2H3,(H,27,28)(H,29,30)/t18-/m0/s1\",[C][O][C][=C][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][C][=C][C][=C][Branch2][Ring1][N][C][C@H1][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][=Branch1],\"(2s)-2-[(2,6-dichlorobenzoyl)amino]-3-[4-(2,6-dimethoxyphenyl)phenyl]propanoic acid\",-0.27\nCOc1ccccc1Oc2c(NS(=O)(=O)c3ccc(cc3)C(C)(C)C)nc(nc2OCCO)c4ncccn4,\"InChI=1S/C27H29N5O6S/c1-27(2,3)18-10-12-19(13-11-18)39(34,35)32-23-22(38-21-9-6-5-8-20(21)36-4)26(37-17-16-33)31-25(30-23)24-28-14-7-15-29-24/h5-15,33H,16-17H2,1-4H3,(H,30,31,32)\",[C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][Branch2][Ring1][O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][N][=C][Branch1][#Branch2][N][=C][Ring2][Ring1][Ring2][O][C][C][O][C][=N][C][=C][C][=N][Ring1][=Branch1],4-tert-butyl-n-[6-(2-hydroxyethoxy)-5-(2-methoxyphenoxy)-2-pyrimidin-2-ylpyrimidin-4-yl]benzenesulfonamide,1.03\nOC(C(=O)c1ccccc1)c2ccccc2,\"InChI=1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H\",[O][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-hydroxy-1,2-di(phenyl)ethanone\",2.13\nCC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN2CCC3(CC2)Cc4cc(F)ccc4O3,\"InChI=1S/C23H27FN2O5/c1-15(27)25-20-4-3-18(28)11-22(20)30-14-19(29)13-26-8-6-23(7-9-26)12-16-10-17(24)2-5-21(16)31-23/h2-5,10-11,19,28-29H,6-9,12-14H2,1H3,(H,25,27)/t19-/m0/s1\",[C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][C@@H1][Branch1][C][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][O][Ring1][N],\"n-[2-[(2s)-3-(5-fluorospiro[3h-1-benzofuran-2,4'-piperidine]-1'-yl)-2-hydroxypropoxy]-4-hydroxyphenyl]acetamide\",2.1\nCOc1cc2ncc(C(=O)N)c(Nc3ccc(C)cc3F)c2cc1OC,\"InChI=1S/C19H18FN3O3/c1-10-4-5-14(13(20)6-10)23-18-11-7-16(25-2)17(26-3)8-15(11)22-9-12(18)19(21)24/h4-9H,1-3H3,(H2,21,24)(H,22,23)\",[C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C],\"4-[(2-fluoro-4-methylphenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\",3.34\nCN1CCN(CC1)S(=O)(=O)c2ccc(cc2)c3cnc(N)c(n3)C(=O)Nc4cnccc4CN5CCCC5,\"InChI=1S/C26H32N8O3S/c1-32-12-14-34(15-13-32)38(36,37)21-6-4-19(5-7-21)23-17-29-25(27)24(30-23)26(35)31-22-16-28-9-8-20(22)18-33-10-2-3-11-33/h4-9,16-17H,2-3,10-15,18H2,1H3,(H2,27,29)(H,31,35)\",[C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][N][=C][C][=C][Ring1][=Branch1][C][N][C][C][C][C][Ring1][Branch1],3-amino-6-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-[4-(pyrrolidin-1-ylmethyl)pyridin-3-yl]pyrazine-2-carboxamide,3.28\nN[C@@H](Cc1ccc(F)cc1)C(=O)O,\"InChI=1S/C9H10FNO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m0/s1\",[N][C@@H1][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][O],(2s)-2-amino-3-(4-fluorophenyl)propanoic acid,-1.06\nCN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)C(CO)c3ccccc3,\"InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15+,16?\",[C][N][C@@H1][C][C][C@H1][Ring1][Branch1][C][C@H1][Branch1][Ring2][C][Ring1][#Branch1][O][C][=Branch1][C][=O][C][Branch1][Ring1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"[(1r,5s)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate\",-0.66\nBrc1ccc(cc1)C2NC(=O)c3ccccc3N2,\"InChI=1S/C14H11BrN2O/c15-10-7-5-9(6-8-10)13-16-12-4-2-1-3-11(12)14(18)17-13/h1-8,13,16H,(H,17,18)\",[Br][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O],\"2-(4-bromophenyl)-2,3-dihydro-1h-quinazolin-4-one\",2.68\nCOc1cc(nc2c(cc(F)cc12)N3CCN(C)CC3)C(=O)Nc4ccc(cc4)N5CCOCC5,\"InChI=1S/C26H30FN5O3/c1-30-7-9-32(10-8-30)23-16-18(27)15-21-24(34-2)17-22(29-25(21)23)26(33)28-19-3-5-20(6-4-19)31-11-13-35-14-12-31/h3-6,15-17H,7-14H2,1-2H3,(H,28,33)\",[C][O][C][=C][C][=Branch2][Ring1][N][=N][C][=C][Branch1][N][C][=C][Branch1][C][F][C][=C][Ring1][O][Ring1][#Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],6-fluoro-4-methoxy-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)quinoline-2-carboxamide,3.85\nCCCC(=O)Nc1ccc(OCC(O)CNC(C)C)c(c1)C(=O)C,\"InChI=1S/C18H28N2O4/c1-5-6-18(23)20-14-7-8-17(16(9-14)13(4)21)24-11-15(22)10-19-12(2)3/h7-9,12,15,19,22H,5-6,10-11H2,1-4H3,(H,20,23)\",[C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=C][O][C][C][Branch1][C][O][C][N][C][Branch1][C][C][C][C][=Branch1][Ring2][=C][Ring1][#C][C][=Branch1][C][=O][C],n-[3-acetyl-4-[2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]butanamide,-0.27\nOC(=O)C1CCn2c1ccc2C(=O)c3ccccc3,\"InChI=1S/C15H13NO3/c17-14(10-4-2-1-3-5-10)13-7-6-12-11(15(18)19)8-9-16(12)13/h1-7,11H,8-9H2,(H,18,19)\",[O][C][=Branch1][C][=O][C][C][C][N][C][Ring1][Branch1][=C][C][=C][Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-(benzoyl)-2,3-dihydro-1h-pyrrolizine-1-carboxylic acid\",-0.93\nCN1C2CCC1CC(C2)OC(=O)C(CO)c3ccccc3,\"InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3\",[C][N][C][C][C][C][Ring1][Branch1][C][C][Branch1][Ring2][C][Ring1][#Branch1][O][C][=Branch1][C][=O][C][Branch1][Ring1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1],(8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate,-0.09\nCC(=O)c1ccc(cc1)S(=O)(=O)NC(=O)NC2CCCCC2,\"InChI=1S/C15H20N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-10,13H,2-6H2,1H3,(H2,16,17,19)\",[C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1],3-(4-acetylphenyl)sulfonyl-1-cyclohexylurea,-0.49\nNC(=O)Nc1sc(cc1C(=O)N)c2ccc(CN3CCCCC3)cc2,\"InChI=1S/C18H22N4O2S/c19-16(23)14-10-15(25-17(14)21-18(20)24)13-6-4-12(5-7-13)11-22-8-2-1-3-9-22/h4-7,10H,1-3,8-9,11H2,(H2,19,23)(H3,20,21,24)\",[N][C][=Branch1][C][=O][N][C][S][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][=N],2-(carbamoylamino)-5-[4-(piperidin-1-ylmethyl)phenyl]thiophene-3-carboxamide,1.75\nCc1oc(CN2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4,\"InChI=1S/C22H33N3O2/c1-15-20(9-19(27-15)13-25-4-2-23-3-5-25)21(26)24-14-22-10-16-6-17(11-22)8-18(7-16)12-22/h9,16-18,23H,2-8,10-14H2,1H3,(H,24,26)\",[C][C][O][C][Branch1][#Branch2][C][N][C][C][N][C][C][Ring1][=Branch1][=C][C][=Ring1][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-methyl-5-(piperazin-1-ylmethyl)furan-3-carboxamide,1.03\nC[C@H](CO)Nc1nc(SCc2ccccc2F)nc3NC(=O)Sc13,\"InChI=1S/C15H15FN4O2S2/c1-8(6-21)17-12-11-13(20-15(22)24-11)19-14(18-12)23-7-9-4-2-3-5-10(9)16/h2-5,8,21H,6-7H2,1H3,(H2,17,18,19,20,22)/t8-/m1/s1\",[C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][N][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1],\"5-[(2-fluorophenyl)methylsulfanyl]-7-[[(2r)-1-hydroxypropan-2-yl]amino]-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\",3\nOC(=O)COc1ccc(Br)cc1c2ccccc2,\"InChI=1S/C14H11BrO3/c15-11-6-7-13(18-9-14(16)17)12(8-11)10-4-2-1-3-5-10/h1-8H,9H2,(H,16,17)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],2-(4-bromo-2-phenylphenoxy)acetic acid,0.15\nCc1sc(N)nc1c2ccccc2,\"InChI=1S/C10H10N2S/c1-7-9(12-10(11)13-7)8-5-3-2-4-6-8/h2-6H,1H3,(H2,11,12)\",[C][C][S][C][Branch1][C][N][=N][C][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"5-methyl-4-phenyl-1,3-thiazol-2-amine\",2.75\nNc1ccccc1[N+](=O)[O-],\"InChI=1S/C6H6N2O2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H,7H2\",[N][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1],2-nitroaniline,-0.96\nC1CN2CCC1C(=C2)c3oc4ccccc4c3,\"InChI=1S/C15H15NO/c1-2-4-14-12(3-1)9-15(17-14)13-10-16-7-5-11(13)6-8-16/h1-4,9-11H,5-8H2\",[C][C][N][C][C][C][Ring1][=Branch1][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2],3-(1-benzofuran-2-yl)-1-azabicyclo[2.2.2]oct-2-ene,2.59\nNc1ccc2c3ccccc3C(=O)c2c1,\"InChI=1S/C13H9NO/c14-8-5-6-10-9-3-1-2-4-11(9)13(15)12(10)7-8/h1-7H,14H2\",[N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring1][#Branch2][=C][Ring1][=C],2-aminofluoren-9-one,2.9\nClc1ccc(CNc2nc(nc3ncccc23)N4CCN(CC4)C(=O)[C@H]5CCCCN5)c(Cl)c1,\"InChI=1S/C24H27Cl2N7O/c25-17-7-6-16(19(26)14-17)15-29-22-18-4-3-9-28-21(18)30-24(31-22)33-12-10-32(11-13-33)23(34)20-5-1-2-8-27-20/h3-4,6-7,9,14,20,27H,1-2,5,8,10-13,15H2,(H,28,29,30,31)/t20-/m1/s1\",[Cl][C][=C][C][=C][Branch2][Ring2][=Branch2][C][N][C][=N][C][=Branch1][N][=N][C][=N][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][C][C][C][C][N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][P],\"[4-[4-[(2,4-dichlorophenyl)methylamino]pyrido[3,2-e]pyrimidin-2-yl]piperazin-1-yl]-[(2r)-piperidin-2-yl]methanone\",2.27\nCN1CCN(CCOc2n[nH]c3ncnc(Nc4ccc(OCc5ccccn5)c(Cl)c4)c23)CC1,\"InChI=1S/C24H27ClN8O2/c1-32-8-10-33(11-9-32)12-13-34-24-21-22(27-16-28-23(21)30-31-24)29-17-5-6-20(19(25)14-17)35-15-18-4-2-3-7-26-18/h2-7,14,16H,8-13,15H2,1H3,(H2,27,28,29,30,31)\",[C][N][C][C][N][Branch2][Ring2][=C][C][C][O][C][=N][NH1][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring1][#C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=Branch1][C][C][Ring2][Ring2][C],\"n-[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]-3-[2-(4-methylpiperazin-1-yl)ethoxy]-1h-pyrazolo[4,5-e]pyrimidin-4-amine\",2.45\nNC(=O)N1c2ccccc2C=Cc3ccccc13,\"InChI=1S/C15H12N2O/c16-15(18)17-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)17/h1-10H,(H2,16,18)\",[N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1],benzo[b][1]benzazepine-11-carboxamide,1.65\nCC(C)Oc1cccc(CC(=O)N2CCC[C@@](CC[N+]34CCC(CC3)(CC4)c5ccccc5)(C2)c6ccc(Cl)c(Cl)c6)c1,\"InChI=1S/C37H45Cl2N2O2/c1-28(2)43-32-11-6-8-29(24-32)25-35(42)40-19-7-14-37(27-40,31-12-13-33(38)34(39)26-31)18-23-41-20-15-36(16-21-41,17-22-41)30-9-4-3-5-10-30/h3-6,8-13,24,26,28H,7,14-23,25,27H2,1-2H3/q+1/t36?,37-,41?/m1/s1\",[C][C][Branch1][C][C][O][C][=C][C][=C][C][Branch2][Branch1][N][C][C][=Branch1][C][=O][N][C][C][C][C@@][Branch2][Ring1][O][C][C][N+1][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][Branch1][Branch1][C][C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Branch1][Branch1][C][Ring2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring2][Ring2][#Branch1],\"1-[(3s)-3-(3,4-dichlorophenyl)-3-[2-(4-phenyl-1-azoniabicyclo[2.2.2]octan-1-yl)ethyl]piperidin-1-yl]-2-(3-propan-2-yloxyphenyl)ethanone\",1.23\nCOc1nc(Br)cnc1NS(=O)(=O)c2ccc(Cl)s2,\"InChI=1S/C9H7BrClN3O3S2/c1-17-9-8(12-4-5(10)13-9)14-19(15,16)7-3-2-6(11)18-7/h2-4H,1H3,(H,12,14)\",[C][O][C][=N][C][Branch1][C][Br][=C][N][=C][Ring1][#Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1],n-(5-bromo-3-methoxypyrazin-2-yl)-5-chlorothiophene-2-sulfonamide,0.99\nCc1onc(c2ccccc2)c1c3ccc(cc3)S(=O)(=O)N,\"InChI=1S/C16H14N2O3S/c1-11-15(12-7-9-14(10-8-12)22(17,19)20)16(18-21-11)13-5-3-2-4-6-13/h2-10H,1H3,(H2,17,19,20)\",[C][C][O][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N],\"4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzenesulfonamide\",2.37\nO=C1NC(=O)C(Cc2cccc(Oc3ccccc3)c2)S1,\"InChI=1S/C16H13NO3S/c18-15-14(21-16(19)17-15)10-11-5-4-8-13(9-11)20-12-6-2-1-3-7-12/h1-9,14H,10H2,(H,17,18,19)\",[O][=C][N][C][=Branch1][C][=O][C][Branch2][Ring1][Branch1][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][S][Ring2][Ring1][Ring2],\"5-[[3-(phenoxy)phenyl]methyl]-1,3-thiazolidine-2,4-dione\",2.84\nOCCNC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3,\"InChI=1S/C20H19ClN4O4S/c21-16-9-12-8-13(24-19(12)30-16)18(28)23-14-7-11-3-1-2-4-15(11)25(20(14)29)10-17(27)22-5-6-26/h1-4,8-9,14,24,26H,5-7,10H2,(H,22,27)(H,23,28)\",[O][C][C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2],\"2-chloro-n-[1-[2-(2-hydroxyethylamino)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\",3.05\nClc1ccc2OCOc2c1Nc3ncnc4cc(OCCCN5CCCC5)cc(OC6CCOCC6)c34,\"InChI=1S/C27H31ClN4O5/c28-20-4-5-22-26(36-17-35-22)25(20)31-27-24-21(29-16-30-27)14-19(34-11-3-10-32-8-1-2-9-32)15-23(24)37-18-6-12-33-13-7-18/h4-5,14-16,18H,1-3,6-13,17H2,(H,29,30,31)\",[Cl][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][=N][C][=N][C][=C][C][Branch1][N][O][C][C][C][N][C][C][C][C][Ring1][Branch1][=C][C][Branch1][#Branch2][O][C][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1],\"n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine\",2.3\nCC(C)C(NC(=O)CN1C(=O)C2=C(C=C1c3ccccc3)C(=O)N(CCN4CCOCC4)C(=O)N2)C(=O)C(F)(F)F,\"InChI=1S/C27H30F3N5O6/c1-16(2)21(23(37)27(28,29)30)31-20(36)15-35-19(17-6-4-3-5-7-17)14-18-22(25(35)39)32-26(40)34(24(18)38)9-8-33-10-12-41-13-11-33/h3-7,14,16,21H,8-13,15H2,1-2H3,(H,31,36)(H,32,40)\",[C][C][Branch1][C][C][C][Branch2][Branch1][Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=C][Branch1][=N][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring2][Ring1][Branch2][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[3-(2-morpholin-4-ylethyl)-2,4,8-trioxo-6-phenyl-1h-pyrido[3,4-d]pyrimidin-7-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.91\nCc1[nH]c(C(=O)NC2CCN(CC2)c3ncc(s3)C(=O)O)c(Cl)c1Cl,\"InChI=1S/C15H16Cl2N4O3S/c1-7-10(16)11(17)12(19-7)13(22)20-8-2-4-21(5-3-8)15-18-6-9(25-15)14(23)24/h6,8,19H,2-5H2,1H3,(H,20,22)(H,23,24)\",[C][C][NH1][C][Branch2][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=Branch1][C][=O][O][=C][Branch1][C][Cl][C][=Ring2][Ring1][#Branch1][Cl],\"2-[4-[(3,4-dichloro-5-methyl1h-pyrrole-2-carbonyl)amino]piperidin-1-yl]-1,3-thiazole-5-carboxylic acid\",0.02\nCC(C)CCOc1ccc(N)cc1,\"InChI=1S/C11H17NO/c1-9(2)7-8-13-11-5-3-10(12)4-6-11/h3-6,9H,7-8,12H2,1-2H3\",[C][C][Branch1][C][C][C][C][O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1],4-(3-methylbutoxy)aniline,2.67\nCc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(C)cccc34,\"InChI=1S/C22H20N2O2/c1-13-7-8-19-18(11-13)21(15(3)24(19)12-20(25)26)16-9-10-23-22-14(2)5-4-6-17(16)22/h4-11H,12H2,1-3H3,(H,25,26)\",[C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][O][Ring1][#Branch1],\"2-[2,5-dimethyl-3-(8-methylquinolin-4-yl)indol-1-yl]acetic acid\",1.29\nFc1ccccc1Nc2oc(nn2)C(=O)Nc3ccc(Oc4cccnc4)nc3,\"InChI=1S/C19H13FN6O3/c20-14-5-1-2-6-15(14)24-19-26-25-18(29-19)17(27)23-12-7-8-16(22-10-12)28-13-4-3-9-21-11-13/h1-11H,(H,23,27)(H,24,26)\",[F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][=C][Ring1][=N],\"5-[(2-fluorophenyl)amino]-n-(6-pyridin-3-yloxypyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\",3.1\nCN(C)CCCOc1nn(Cc2ccccc2)c3ccccc13,\"InChI=1S/C19H23N3O/c1-21(2)13-8-14-23-19-17-11-6-7-12-18(17)22(20-19)15-16-9-4-3-5-10-16/h3-7,9-12H,8,13-15H2,1-2H3\",[C][N][Branch1][C][C][C][C][C][O][C][=N][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1],\"n,n-dimethyl-3-[1-(phenylmethyl)indazol-3-yl]oxypropan-1-amine\",2.4\nCc1ccc(cc1)c2nnc(N3CCN(CC3)C(=O)c4occc4)c5ccccc25,\"InChI=1S/C24H22N4O2/c1-17-8-10-18(11-9-17)22-19-5-2-3-6-20(19)23(26-25-22)27-12-14-28(15-13-27)24(29)21-7-4-16-30-21/h2-11,16H,12-15H2,1H3\",[C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][=C][Branch2][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][#Branch1][Ring1][=Branch1],furan-2-yl-[4-[4-(4-methylphenyl)phthalazin-1-yl]piperazin-1-yl]methanone,3.78\nCOc1ccc(OC)c(CNc2n[nH]c3ccnc(Oc4ccccc4)c23)c1,\"InChI=1S/C21H20N4O3/c1-26-16-8-9-18(27-2)14(12-16)13-23-20-19-17(24-25-20)10-11-22-21(19)28-15-6-4-3-5-7-15/h3-12H,13H2,1-2H3,(H2,23,24,25)\",[C][O][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch2][Ring1][O][C][N][C][=N][NH1][C][=C][C][=N][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][S][Ring1][=N][=C][Ring2][Ring1][#Branch2],\"n-[(2,5-dimethoxyphenyl)methyl]-4-(phenoxy)-1h-pyrazolo[4,5-c]pyridin-3-amine\",4.25\nCC(C)Cc1ccc(cc1)[C@H](C)C(=O)NS(=O)(=O)C,\"InChI=1S/C14H21NO3S/c1-10(2)9-12-5-7-13(8-6-12)11(3)14(16)15-19(4,17)18/h5-8,10-11H,9H2,1-4H3,(H,15,16)/t11-/m0/s1\",[C][C][Branch1][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@H1][Branch1][C][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C],(2s)-2-[4-(2-methylpropyl)phenyl]-n-methylsulfonylpropanamide,0.56\nNC(=O)Nc1cc(sc1C(=O)N)c2ccsc2,\"InChI=1S/C10H9N3O2S2/c11-9(14)8-6(13-10(12)15)3-7(17-8)5-1-2-16-4-5/h1-4H,(H2,11,14)(H3,12,13,15)\",[N][C][=Branch1][C][=O][N][C][C][=C][Branch1][#Branch2][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][C][=C][S][C][=Ring1][Branch1],3-(carbamoylamino)-5-thiophen-3-ylthiophene-2-carboxamide,2.3\nCOc1cc(OC2CCN(C)CC2)c3c(Nc4cccc5OCCOc45)ncnc3c1,\"InChI=1S/C23H26N4O4/c1-27-8-6-15(7-9-27)31-20-13-16(28-2)12-18-21(20)23(25-14-24-18)26-17-4-3-5-19-22(17)30-11-10-29-19/h3-5,12-15H,6-11H2,1-2H3,(H,24,25,26)\",[C][O][C][=C][C][Branch1][=N][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][C][Branch1][S][N][C][=C][C][=C][C][O][C][C][O][C][Ring1][#Branch2][=Ring1][=Branch1][=N][C][=N][C][Ring1][P][=C][Ring2][Ring1][=N],\"n-(2,3-dihydro-1,4-benzodioxin-8-yl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine\",2.26\nNc1sc2CCCCc2c1C(=O)NCc3ccccc3,\"InChI=1S/C16H18N2OS/c17-15-14(12-8-4-5-9-13(12)20-15)16(19)18-10-11-6-2-1-3-7-11/h1-3,6-7H,4-5,8-10,17H2,(H,18,19)\",[N][C][S][C][C][C][C][C][C][=Ring1][=Branch1][C][=Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-amino-n-(phenylmethyl)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide\",3.52\nCN1CCC(CC1)Oc2cccc3ncnc(Nc4ccc(OCc5cnccn5)c(Cl)c4)c23,\"InChI=1S/C25H25ClN6O2/c1-32-11-7-19(8-12-32)34-23-4-2-3-21-24(23)25(30-16-29-21)31-17-5-6-22(20(26)13-17)33-15-18-14-27-9-10-28-18/h2-6,9-10,13-14,16,19H,7-8,11-12,15H2,1H3,(H,29,30,31)\",[C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][N][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring1][#C][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1],n-[3-chloro-4-(pyrazin-2-ylmethoxy)phenyl]-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine,3.21\nCC(C)COCC(CN(Cc1ccccc1)c2ccccc2)N3CCCC3,\"InChI=1S/C24H34N2O/c1-21(2)19-27-20-24(25-15-9-10-16-25)18-26(23-13-7-4-8-14-23)17-22-11-5-3-6-12-22/h3-8,11-14,21,24H,9-10,15-20H2,1-2H3\",[C][C][Branch1][C][C][C][O][C][C][Branch2][Ring1][=Branch1][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][C][C][Ring1][Branch1],n-[3-(2-methylpropoxy)-2-pyrrolidin-1-ylpropyl]-n-(phenylmethyl)aniline,3.66\nO[C@H](C[C@H](O)\\C=C\\c1c(nc2ccccc2c1c3ccc(F)cc3)C4CC4)CC(=O)O,\"InChI=1S/C25H24FNO4/c26-17-9-7-15(8-10-17)24-20-3-1-2-4-22(20)27-25(16-5-6-16)21(24)12-11-18(28)13-19(29)14-23(30)31/h1-4,7-12,16,18-19,28-29H,5-6,13-14H2,(H,30,31)/b12-11+/t18-,19-/m1/s1\",[O][C@H1][Branch2][Ring2][=Branch2][C][C@H1][Branch1][C][O][\\C][=C][\\C][=C][Branch2][Ring1][Branch2][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][C][Ring1][Ring1][C][C][=Branch1][C][=O][O],\"(e,3r,5s)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-dihydroxyhept-6-enoic acid\",0.91\nNc1cccc2c3ccccc3C(=O)C(=O)c12,\"InChI=1S/C14H9NO2/c15-11-7-3-6-9-8-4-1-2-5-10(8)13(16)14(17)12(9)11/h1-7H,15H2\",[N][C][=C][C][=C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][Ring1][S][=Ring1][N],\"1-aminophenanthrene-9,10-dione\",2.95\nO=C(NCc1ccncc1)c2ccc(Oc3ccccc3)cc2,\"InChI=1S/C19H16N2O2/c22-19(21-14-15-10-12-20-13-11-15)16-6-8-18(9-7-16)23-17-4-2-1-3-5-17/h1-13H,14H2,(H,21,22)\",[O][=C][Branch1][O][N][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N],4-(phenoxy)-n-(pyridin-4-ylmethyl)benzamide,3.26\nOC(=O)COc1ccc(Cl)cc1CN2CCN(CC2)S(=O)(=O)Cc3ccccc3,\"InChI=1S/C20H23ClN2O5S/c21-18-6-7-19(28-14-20(24)25)17(12-18)13-22-8-10-23(11-9-22)29(26,27)15-16-4-2-1-3-5-16/h1-7,12H,8-11,13-15H2,(H,24,25)\",[O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-[4-chloro-2-[[4-(phenylmethylsulfonyl)piperazin-1-yl]methyl]phenoxy]acetic acid,0.33\nCN(C)C[C@H](O)Cc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C23H33ClN2O2/c1-26(2)13-19(27)8-15-3-4-21(24)20(9-15)22(28)25-14-23-10-16-5-17(11-23)7-18(6-16)12-23/h3-4,9,16-19,27H,5-8,10-14H2,1-2H3,(H,25,28)/t16?,17?,18?,19-,23?/m1/s1\",[C][N][Branch1][C][C][C][C@H1][Branch1][C][O][C][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chloro-5-[(2r)-3-dimethylamino-2-hydroxypropyl]benzamide,2.19\nCN1CCN(CCCN2c3ccccc3Sc4ccc(cc24)C(F)(F)F)CC1,\"InChI=1S/C21H24F3N3S/c1-25-11-13-26(14-12-25)9-4-10-27-17-5-2-3-6-19(17)28-20-8-7-16(15-18(20)27)21(22,23)24/h2-3,5-8,15H,4,9-14H2,1H3\",[C][N][C][C][N][Branch2][Ring2][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][C][Ring2][Ring1][O],10-[3-(4-methylpiperazin-1-yl)propyl]-2-(trifluoromethyl)phenothiazine,4.31\nCN(C)C(=O)C(CCN1CCC(O)(CC1)c2ccc(Cl)cc2)(c3ccccc3)c4ccccc4,\"InChI=1S/C29H33ClN2O2/c1-31(2)27(33)29(24-9-5-3-6-10-24,25-11-7-4-8-12-25)19-22-32-20-17-28(34,18-21-32)23-13-15-26(30)16-14-23/h3-16,34H,17-22H2,1-2H3\",[C][N][Branch1][C][C][C][=Branch1][C][=O][C][Branch2][Ring1][O][C][C][N][C][C][C][Branch1][C][O][Branch1][Branch1][C][C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-n,n-dimethyl-2,2-di(phenyl)butanamide\",3.47\nCN(C)CCCOc1nccc(Nc2cc(NC(=O)c3ccnc(c3)N4CCOCC4)ccc2C)n1,\"InChI=1S/C26H33N7O3/c1-19-5-6-21(29-25(34)20-7-9-27-24(17-20)33-12-15-35-16-13-33)18-22(19)30-23-8-10-28-26(31-23)36-14-4-11-32(2)3/h5-10,17-18H,4,11-16H2,1-3H3,(H,29,34)(H,28,30,31)\",[C][N][Branch1][C][C][C][C][C][O][C][=N][C][=C][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=N][Ring2][Ring1][=N],n-[3-[[2-(3-dimethylaminopropoxy)pyrimidin-4-yl]amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide,1.3\nNNC(=O)c1ccncc1,\"InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)\",[N][N][C][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1],pyridine-4-carbohydrazide,-0.57\nCCS(=O)(=O)c1ccc(cc1)c2cc(Cl)ccc2OCC(=O)O,\"InChI=1S/C16H15ClO5S/c1-2-23(20,21)13-6-3-11(4-7-13)14-9-12(17)5-8-15(14)22-10-16(18)19/h3-9H,2,10H2,1H3,(H,18,19)\",[C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O],2-[4-chloro-2-(4-ethylsulfonylphenyl)phenoxy]acetic acid,-0.78\nCc1cccc(Nc2ncnc3ccccc23)c1,\"InChI=1S/C15H13N3/c1-11-5-4-6-12(9-11)18-15-13-7-2-3-8-14(13)16-10-17-15/h2-10H,1H3,(H,16,17,18)\",[C][C][=C][C][=C][C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][P],n-(3-methylphenyl)quinazolin-4-amine,3.21\nOCCCNCCCOc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3,\"InChI=1S/C24H35ClN2O3/c25-22-4-3-20(30-8-2-6-26-5-1-7-28)12-21(22)23(29)27-16-24-13-17-9-18(14-24)11-19(10-17)15-24/h3-4,12,17-19,26,28H,1-2,5-11,13-16H2,(H,27,29)\",[O][C][C][C][N][C][C][C][O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2],n-(1-adamantylmethyl)-2-chloro-5-[3-(3-hydroxypropylamino)propoxy]benzamide,1.41\nC[C@H]1C[C@H]2[C@@H]3CC[C@H](C(=O)C)[C@@]3(C)C[C@H](O)[C@@H]2[C@@]4(C)CCC(=O)C=C14,\"InChI=1S/C22H32O3/c1-12-9-15-17-6-5-16(13(2)23)22(17,4)11-19(25)20(15)21(3)8-7-14(24)10-18(12)21/h10,12,15-17,19-20,25H,5-9,11H2,1-4H3/t12-,15-,16+,17-,19-,20+,21-,22+/m0/s1\",[C][C@H1][C][C@H1][C@@H1][C][C][C@H1][Branch1][=Branch1][C][=Branch1][C][=O][C][C@@][Ring1][Branch2][Branch1][C][C][C][C@H1][Branch1][C][O][C@@H1][Ring1][=C][C@@][Branch1][C][C][C][C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][Branch2][Ring1][Branch2],\"(6s,8s,9s,10r,11s,13s,14s,17s)-17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one\",3.25\nFc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)N3CCOCC3,\"InChI=1S/C17H21FN2O3/c18-15-3-1-13(2-4-15)16(21)14-5-7-19(8-6-14)17(22)20-9-11-23-12-10-20/h1-4,14H,5-12H2\",[F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1],[4-(4-fluorobenzoyl)piperidin-1-yl]-morpholin-4-ylmethanone,1.61\nCC1CN(CCN1)C(=O)c2cc3ccccc3[nH]2,\"InChI=1S/C14H17N3O/c1-10-9-17(7-6-15-10)14(18)13-8-11-4-2-3-5-12(11)16-13/h2-5,8,10,15-16H,6-7,9H2,1H3\",[C][C][C][N][Branch1][=Branch1][C][C][N][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],1h-indol-2-yl-(3-methylpiperazin-1-yl)methanone,0.94\nCCOc1ccc(cc1)c2cnc3CCCCCn23,\"InChI=1S/C16H20N2O/c1-2-19-14-9-7-13(8-10-14)15-12-17-16-6-4-3-5-11-18(15)16/h7-10,12H,2-6,11H2,1H3\",[C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][C][C][C][C][C][N][Ring1][#Branch2][Ring1][#Branch1],\"3-(4-ethoxyphenyl)-6,7,8,9-tetrahydro-5h-imidazo[1,2-a]azepine\",3.01\nOCC(O)COC(=O)c1ccccc1Nc2ccnc3cc(Cl)ccc23,\"InChI=1S/C19H17ClN2O4/c20-12-5-6-14-17(7-8-21-18(14)9-12)22-16-4-2-1-3-15(16)19(25)26-11-13(24)10-23/h1-9,13,23-24H,10-11H2,(H,21,22)\",[O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1],\"2,3-dihydroxypropyl 2-[(7-chloroquinolin-4-yl)amino]benzoate\",3.5\nC1CN2CCC1C(C2)c3ccc(cc3)c4ccccc4,\"InChI=1S/C19H21N/c1-2-4-15(5-3-1)16-6-8-17(9-7-16)19-14-20-12-10-18(19)11-13-20/h1-9,18-19H,10-14H2\",[C][C][N][C][C][C][Ring1][=Branch1][C][Branch1][Ring2][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],8-(4-phenylphenyl)-1-azabicyclo[2.2.2]octane,1.76\nCc1cc(NC(=O)c2oc(Nc3ccccc3F)nn2)ccc1N4CCOCC4,\"InChI=1S/C20H20FN5O3/c1-13-12-14(6-7-17(13)26-8-10-28-11-9-26)22-18(27)19-24-25-20(29-19)23-16-5-3-2-4-15(16)21/h2-7,12H,8-11H2,1H3,(H,22,27)(H,23,25)\",[C][C][=C][C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][O][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][N][=Ring1][=N][=C][C][=C][Ring2][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"5-[(2-fluorophenyl)amino]-n-(3-methyl-4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\",4\nNc1ccc(cc1)S(=O)(=O)Nc2ccccn2,\"InChI=1S/C11H11N3O2S/c12-9-4-6-10(7-5-9)17(15,16)14-11-3-1-2-8-13-11/h1-8H,12H2,(H,13,14)\",[N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1],4-amino-n-pyridin-2-ylbenzenesulfonamide,-0.01\nClc1cc(Cl)c2c3C(=O)NNC(=O)c3[nH]c2c1,\"InChI=1S/C10H5Cl2N3O2/c11-3-1-4(12)6-5(2-3)13-8-7(6)9(16)14-15-10(8)17/h1-2,13H,(H,14,16)(H,15,17)\",[Cl][C][=C][C][Branch1][C][Cl][=C][C][C][=Branch1][C][=O][N][N][C][=Branch1][C][=O][C][=Ring1][Branch2][NH1][C][Ring1][O][=C][Ring1][S],\"7,9-dichloro-3,5-dihydro-2h-pyridazino[4,5-b]indole-1,4-dione\",1.02\nFc1cccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)c1,\"InChI=1S/C18H17FN6O3/c19-12-2-1-3-13(10-12)22-18-24-23-17(28-18)16(26)21-14-4-5-15(20-11-14)25-6-8-27-9-7-25/h1-5,10-11H,6-9H2,(H,21,26)(H,22,24)\",[F][C][=C][C][=C][C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][O],\"5-[(3-fluorophenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\",3.2\nCN(C)CC(O)COc1ccc(Nc2nccc(Nc3cc(C)ccc3F)n2)cc1,\"InChI=1S/C22H26FN5O2/c1-15-4-9-19(23)20(12-15)26-21-10-11-24-22(27-21)25-16-5-7-18(8-6-16)30-14-17(29)13-28(2)3/h4-12,17,29H,13-14H2,1-3H3,(H2,24,25,26,27)\",[C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][F][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1],1-dimethylamino-3-[4-[[4-[(2-fluoro-5-methylphenyl)amino]pyrimidin-2-yl]amino]phenoxy]propan-2-ol,2.1\nO=C(NC1CC1)c2cc(on2)c3cccs3,\"InChI=1S/C11H10N2O2S/c14-11(12-7-3-4-7)8-6-9(15-13-8)10-2-1-5-16-10/h1-2,5-7H,3-4H2,(H,12,14)\",[O][=C][Branch1][#Branch1][N][C][C][C][Ring1][Ring1][C][C][=C][Branch1][Branch1][O][N][=Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1],\"n-cyclopropyl-5-thiophen-2-yl-1,2-oxazole-3-carboxamide\",2.54\nCCOc1ccc(NC(=O)CCc2c(C)nc3nc(C)nn3c2C)cc1,\"InChI=1S/C19H23N5O2/c1-5-26-16-8-6-15(7-9-16)22-18(25)11-10-17-12(2)20-19-21-14(4)23-24(19)13(17)3/h6-9H,5,10-11H2,1-4H3,(H,22,25)\",[C][C][O][C][=C][C][=C][Branch2][Ring1][N][N][C][=Branch1][C][=O][C][C][C][C][Branch1][C][C][=N][C][=N][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=Ring1][O][C][C][=C][Ring2][Ring1][#Branch1],\"n-(4-ethoxyphenyl)-3-(2,5,7-trimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)propanamide\",2.1\nNc1nc(N)nc(n1)c2ccc(Cl)cc2,\"InChI=1S/C9H8ClN5/c10-6-3-1-5(2-4-6)7-13-8(11)15-9(12)14-7/h1-4H,(H4,11,12,13,14,15)\",[N][C][=N][C][Branch1][C][N][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"6-(4-chlorophenyl)-1,3,5-triazine-2,4-diamine\",2.12\nCOc1ccc(Nc2cc(Nc3ccc(OCC(O)CN(C)C)cc3)ncn2)cc1,\"InChI=1S/C22H27N5O3/c1-27(2)13-18(28)14-30-20-10-6-17(7-11-20)26-22-12-21(23-15-24-22)25-16-4-8-19(29-3)9-5-16/h4-12,15,18,28H,13-14H2,1-3H3,(H2,23,24,25,26)\",[C][O][C][=C][C][=C][Branch2][Ring2][Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=C][C][=C][Branch1][=N][O][C][C][Branch1][C][O][C][N][Branch1][C][C][C][C][=C][Ring1][=C][=N][C][=N][Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][N],1-dimethylamino-3-[4-[[6-[(4-methoxyphenyl)amino]pyrimidin-4-yl]amino]phenoxy]propan-2-ol,1.5\nO=C(CSc1ccccc1)N2CCN(CC2)C(=O)c3occc3,\"InChI=1S/C17H18N2O3S/c20-16(13-23-14-5-2-1-3-6-14)18-8-10-19(11-9-18)17(21)15-7-4-12-22-15/h1-7,12H,8-11,13H2\",[O][=C][Branch1][O][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1],1-[4-(furan-2-carbonyl)piperazin-1-yl]-2-phenylsulfanylethanone,1.6\nCCN1CCCC1CNC(=O)c2cc(ccc2OC)S(=O)(=O)N,\"InChI=1S/C15H23N3O4S/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21)\",[C][C][N][C][C][C][C][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][N],n-[(1-ethylpyrrolidin-2-yl)methyl]-2-methoxy-5-sulfamoylbenzamide,-1.2\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cc(F)cc(F)c2)N)C(=O)C(F)(F)F,\"InChI=1S/C18H17F5N4O3/c1-8(2)14(15(29)18(21,22)23)26-13(28)7-27-16(25-6-12(24)17(27)30)9-3-10(19)5-11(20)4-9/h3-6,8,14H,7,24H2,1-2H3,(H,26,28)\",[C][C][Branch1][C][C][C][Branch2][Ring2][Ring2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][Ring2][=C][N][=C][Ring1][#Branch1][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-[5-amino-2-(3,5-difluorophenyl)-6-oxopyrimidin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",1.38\nCC(C)N(C(C)C)c1nnc(N)s1,\"InChI=1S/C8H16N4S/c1-5(2)12(6(3)4)8-11-10-7(9)13-8/h5-6H,1-4H3,(H2,9,10)\",[C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1],\"n,n-di(propan-2-yl)-1,3,4-thiadiazole-2,5-diamine\",1.49\nNc1ccc(OCc2ccccc2)cc1,\"InChI=1S/C13H13NO/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9H,10,14H2\",[N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=C],4-(phenylmethoxy)aniline,2.2\nNNCCc1ccccc1,\"InChI=1S/C8H12N2/c9-10-7-6-8-4-2-1-3-5-8/h1-5,10H,6-7,9H2\",[N][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1],2-phenylethylhydrazine,-0.01\nCC1(C)NC(=O)N(C1=O)c2ccc(c(c2)C(F)(F)F)[N+](=O)[O-],\"InChI=1S/C12H10F3N3O4/c1-11(2)9(19)17(10(20)16-11)6-3-4-8(18(21)22)7(5-6)12(13,14)15/h3-5H,1-2H3,(H,16,20)\",[C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][#C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][N+1][=Branch1][C][=O][O-1],\"5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione\",1.74\nNS(=O)(=O)c1ccc2NC(C3CC=CC3c2c1)c4cccc5ccccc45,\"InChI=1S/C22H20N2O2S/c23-27(25,26)15-11-12-21-20(13-15)17-8-4-10-19(17)22(24-21)18-9-3-6-14-5-1-2-7-16(14)18/h1-9,11-13,17,19,22,24H,10H2,(H2,23,25,26)\",[N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][N][C][Branch1][=C][C][C][C][=C][C][Ring1][Branch1][C][Ring1][=Branch2][=C][Ring1][=N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1],\"4-naphthalen-1-yl-3a,4,5,9b-tetrahydro-3h-cyclopenta[c]quinoline-8-sulfonamide\",1.9\nCC[C@H](NC(=O)c1c([S+](C)[O-])c(nc2ccccc12)c3ccccc3)c4ccccc4,\"InChI=1S/C26H24N2O2S/c1-3-21(18-12-6-4-7-13-18)28-26(29)23-20-16-10-11-17-22(20)27-24(25(23)31(2)30)19-14-8-5-9-15-19/h4-17,21H,3H2,1-2H3,(H,28,29)/t21-,31?/m0/s1\",[C][C][C@H1][Branch2][Ring2][Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][=Branch1][S+1][Branch1][C][C][O-1][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],3-methylsulfinyl-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide,3.17\nCc1ccnc(NCc2ccccc2O)c1,\"InChI=1S/C13H14N2O/c1-10-6-7-14-13(8-10)15-9-11-4-2-3-5-12(11)16/h2-8,16H,9H2,1H3,(H,14,15)\",[C][C][=C][C][=N][C][Branch1][N][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][=C][Ring1][#C],2-[[(4-methylpyridin-2-yl)amino]methyl]phenol,3.35\nO[C@@H](CNCCCSCCOCCc1cccc2ccccc12)c3ccc(O)c4NC(=O)Sc34,\"InChI=1S/C26H30N2O4S2/c29-22-10-9-21(25-24(22)28-26(31)34-25)23(30)17-27-12-4-15-33-16-14-32-13-11-19-7-3-6-18-5-1-2-8-20(18)19/h1-3,5-10,23,27,29-30H,4,11-17H2,(H,28,31)/t23-/m0/s1\",[O][C@@H1][Branch2][Ring1][#Branch2][C][N][C][C][C][S][C][C][O][C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-naphthalen-1-ylethoxy)ethylsulfanyl]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\",3.12\nCOc1ccc(cc1)c2nc(N)s[n+]2c3ccccc3,\"InChI=1S/C15H13N3OS/c1-19-13-9-7-11(8-10-13)14-17-15(16)20-18(14)12-5-3-2-4-6-12/h2-10,16H,1H3/p+1\",[C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=C][Branch1][C][N][S][N+1][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1],\"3-(4-methoxyphenyl)-2-phenyl-1,2,4-thiadiazol-2-ium-5-amine\",2.19\nCC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2cccnc2)C(F)(F)F,\"InChI=1S/C15H13F3N2O4S/c1-14(22,15(16,17)18)13(21)20-10-4-6-11(7-5-10)25(23,24)12-3-2-8-19-9-12/h2-9,22H,1H3,(H,20,21)\",[C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"3,3,3-trifluoro-2-hydroxy-2-methyl-n-(4-pyridin-3-ylsulfonylphenyl)propanamide\",2.08\nCOC(=O)Nc1nc2ccc(cc2[nH]1)C(=O)c3ccccc3,\"InChI=1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)\",[C][O][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1],methyl n-[6-(benzoyl)-1h-benzimidazol-2-yl]carbamate,2.9\nFc1cc(ccc1C2=CCS(=O)(=O)CC2)N3C[C@H](Cn4nncc4F)OC3=O,\"InChI=1S/C17H16F2N4O4S/c18-15-7-12(1-2-14(15)11-3-5-28(25,26)6-4-11)22-9-13(27-17(22)24)10-23-16(19)8-20-21-23/h1-3,7-8,13H,4-6,9-10H2/t13-/m1/s1\",[F][C][=C][C][=Branch2][Ring1][Ring2][=C][C][=C][Ring1][=Branch1][C][=C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Ring1][Branch2][N][C][C@H1][Branch1][#Branch2][C][N][N][=N][C][=C][Ring1][Branch1][F][O][C][Ring1][N][=O],\"(5r)-3-[4-(1,1-dioxo-3,6-dihydro-2h-thiopyran-4-yl)-3-fluorophenyl]-5-[(5-fluorotriazol-1-yl)methyl]-1,3-oxazolidin-2-one\",3.54\nCC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccccc34)c2C(=O)N5CC[C@@H](O)C5,\"InChI=1S/C26H28N4O4S/c1-15(2)13-30-25-22(23(32)28(3)26(30)34)21(24(33)29-11-9-17(31)14-29)20(35-25)12-16-8-10-27-19-7-5-4-6-18(16)19/h4-8,10,15,17,31H,9,11-14H2,1-3H3/t17-/m1/s1\",[C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][C][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1],\"5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)-6-(quinolin-4-ylmethyl)thieno[3,2-e]pyrimidine-2,4-dione\",1.65\nCC(=O)C1=Cc2ccc(O)cc2OC1=O,\"InChI=1S/C11H8O4/c1-6(12)9-4-7-2-3-8(13)5-10(7)15-11(9)14/h2-5,13H,1H3\",[C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O],3-acetyl-7-hydroxychromen-2-one,0.87\nC[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)NCCN2CCOCC2)C(F)(F)F,\"InChI=1S/C16H21ClF3N3O5S/c1-15(25,16(18,19)20)14(24)22-13-3-2-11(10-12(13)17)29(26,27)21-4-5-23-6-8-28-9-7-23/h2-3,10,21,25H,4-9H2,1H3,(H,22,24)/t15-/m1/s1\",[C][C@@][Branch1][C][O][Branch2][Ring2][Ring1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F],\"(2r)-n-[2-chloro-4-(2-morpholin-4-ylethylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\",2.14\n[O-][N+](=O)c1cccc2C(=O)C(=O)c3ccccc3c12,InChI=1S/C14H7NO4/c16-13-9-5-2-1-4-8(9)12-10(14(13)17)6-3-7-11(12)15(18)19/h1-7H,[O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][S][=Ring1][N],\"4-nitrophenanthrene-9,10-dione\",2.6\nCC(=O)N[C@@H]1CC2(CCN(Cc3ccc4[nH]c5ccccc5c4c3)CC2)c6ccccc16,\"InChI=1S/C28H29N3O/c1-19(32)29-27-17-28(24-8-4-2-7-22(24)27)12-14-31(15-13-28)18-20-10-11-26-23(16-20)21-6-3-5-9-25(21)30-26/h2-11,16,27,30H,12-15,17-18H2,1H3,(H,29,32)/t27-/m1/s1\",[C][C][=Branch1][C][=O][N][C@@H1][C][C][Branch2][Ring1][S][C][C][N][Branch2][Ring1][Branch1][C][C][=C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=C][Ring1][=N][C][C][Ring2][Ring1][Ring2][C][=C][C][=C][C][=C][Ring2][Ring1][N][Ring1][=Branch1],\"n-[(1r)-1'-(9h-carbazol-3-ylmethyl)spiro[1,2-dihydroindene-3,4'-piperidine]-1-yl]acetamide\",2.96\nCC(C)(C)C(=O)N[C@H]1CCCCNC1=O,\"InChI=1S/C11H20N2O2/c1-11(2,3)10(15)13-8-6-4-5-7-12-9(8)14/h8H,4-7H2,1-3H3,(H,12,14)(H,13,15)/t8-/m0/s1\",[C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][C][N][C][Ring1][#Branch1][=O],\"2,2-dimethyl-n-[(3s)-2-oxoazepan-3-yl]propanamide\",0.58\nO=S(=O)(Nc1cccc2[nH]ncc12)c3cccs3,\"InChI=1S/C11H9N3O2S2/c15-18(16,11-5-2-6-17-11)14-10-4-1-3-9-8(10)7-12-13-9/h1-7,14H,(H,12,13)\",[O][=S][=Branch1][C][=O][Branch1][#C][N][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1],n-(1h-indazol-4-yl)thiophene-2-sulfonamide,1.7\nCOCCNCc1ccc(cc1)c2cc(C(=O)N)c(NC(=O)N)s2,\"InChI=1S/C16H20N4O3S/c1-23-7-6-19-9-10-2-4-11(5-3-10)13-8-12(14(17)21)15(24-13)20-16(18)22/h2-5,8,19H,6-7,9H2,1H3,(H2,17,21)(H3,18,20,22)\",[C][O][C][C][N][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][N][S][Ring1][N],2-(carbamoylamino)-5-[4-[(2-methoxyethylamino)methyl]phenyl]thiophene-3-carboxamide,0.87\nCC(C)N1CCC[C@H](CN2C(=Nc3ccc(Oc4ccc(F)cc4)cc3C2=O)C)C1,\"InChI=1S/C24H28FN3O2/c1-16(2)27-12-4-5-18(14-27)15-28-17(3)26-23-11-10-21(13-22(23)24(28)29)30-20-8-6-19(25)7-9-20/h6-11,13,16,18H,4-5,12,14-15H2,1-3H3/t18-/m0/s1\",[C][C][Branch1][C][C][N][C][C][C][C@H1][Branch2][Ring2][Ring2][C][N][C][=Branch2][Ring1][=N][=N][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][Ring1][=C][C][Ring2][Ring1][C][=O][C][C][Ring2][Ring1][O],6-(4-fluorophenoxy)-2-methyl-3-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]quinazolin-4-one,2.4\nNc1ccc2cn[nH]c2c1,\"InChI=1S/C7H7N3/c8-6-2-1-5-4-9-10-7(5)3-6/h1-4H,8H2,(H,9,10)\",[N][C][=C][C][=C][C][=N][NH1][C][Ring1][Branch1][=C][Ring1][=Branch2],1h-indazol-6-amine,0.52\nFc1ccc(CNC(=O)CCS(=O)(=O)c2ccc(Br)cc2)cc1,\"InChI=1S/C16H15BrFNO3S/c17-13-3-7-15(8-4-13)23(21,22)10-9-16(20)19-11-12-1-5-14(18)6-2-12/h1-8H,9-11H2,(H,19,20)\",[F][C][=C][C][=C][Branch2][Ring1][O][C][N][C][=Branch1][C][=O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch1],3-(4-bromophenyl)sulfonyl-n-[(4-fluorophenyl)methyl]propanamide,3.1\nCC1(CC(=O)NC(=N1)N)c2ccccc2,\"InChI=1S/C11H13N3O/c1-11(8-5-3-2-4-6-8)7-9(15)13-10(12)14-11/h2-6H,7H2,1H3,(H3,12,13,14,15)\",[C][C][Branch1][=C][C][C][=Branch1][C][=O][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1],\"2-amino-6-methyl-6-phenyl-3,5-dihydropyrimidin-4-one\",0.62\nCN(C)C(=O)[C@H](Cc1ccccc1)NC(=O)c2cc3ccccc3[nH]2,\"InChI=1S/C20H21N3O2/c1-23(2)20(25)18(12-14-8-4-3-5-9-14)22-19(24)17-13-15-10-6-7-11-16(15)21-17/h3-11,13,18,21H,12H2,1-2H3,(H,22,24)/t18-/m0/s1\",[C][N][Branch1][C][C][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2],n-[(2s)-1-dimethylamino-1-oxo-3-phenylpropan-2-yl]-1h-indole-2-carboxamide,3.4\nCc1ccc(Oc2ccc(Nc3ncnc4[nH]nc(OCCN5CCC(O)CC5)c34)cc2Cl)cn1,\"InChI=1S/C24H26ClN7O3/c1-15-2-4-18(13-26-15)35-20-5-3-16(12-19(20)25)29-22-21-23(28-14-27-22)30-31-24(21)34-11-10-32-8-6-17(33)7-9-32/h2-5,12-14,17,33H,6-11H2,1H3,(H2,27,28,29,30,31)\",[C][C][=C][C][=C][Branch2][Ring2][=C][O][C][=C][C][=C][Branch2][Ring1][S][N][C][=N][C][=N][C][NH1][N][=C][Branch1][#C][O][C][C][N][C][C][C][Branch1][C][O][C][C][Ring1][#Branch1][C][Ring2][Ring1][Ring1][=Ring1][#C][C][=C][Ring2][Ring1][#Branch2][Cl][C][=N][Ring2][Ring2][C],\"1-[2-[[4-[[3-chloro-4-(6-methylpyridin-3-yl)oxyphenyl]amino]-1h-pyrazolo[4,5-e]pyrimidin-3-yl]oxy]ethyl]piperidin-4-ol\",3.4\nCCCCNc1cc(cc(c1Oc2ccccc2)S(=O)(=O)N)C(=O)O,\"InChI=1S/C17H20N2O5S/c1-2-3-9-19-14-10-12(17(20)21)11-15(25(18,22)23)16(14)24-13-7-5-4-6-8-13/h4-8,10-11,19H,2-3,9H2,1H3,(H,20,21)(H2,18,22,23)\",[C][C][C][C][N][C][=C][C][=Branch2][Ring1][=Branch2][=C][C][=Branch1][=N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][O],3-butylamino-4-(phenoxy)-5-sulfamoylbenzoic acid,-0.3\nCNC(=O)c1cccc(c1c2ccc(CC(C)C)cc2)S(=O)(=O)Nc3ncc(C)nc3OC,\"InChI=1S/C24H28N4O4S/c1-15(2)13-17-9-11-18(12-10-17)21-19(23(29)25-4)7-6-8-20(21)33(30,31)28-22-24(32-5)27-16(3)14-26-22/h6-12,14-15H,13H2,1-5H3,(H,25,29)(H,26,28)\",[C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch2][Ring1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=C][Ring1][#Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][Branch1][C][C][N][=C][Ring1][#Branch1][O][C],3-[(3-methoxy-5-methylpyrazin-2-yl)sulfamoyl]-n-methyl-2-[4-(2-methylpropyl)phenyl]benzamide,1.68\nOc1ccc(cc1)[N+](=O)[O-],\"InChI=1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H\",[O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1],4-nitrophenol,1.5\nOc1cccc2Oc3ccccc3C(=O)c12,\"InChI=1S/C13H8O3/c14-9-5-3-7-11-12(9)13(15)8-4-1-2-6-10(8)16-11/h1-7,14H\",[O][C][=C][C][=C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring1][#C][=Ring1][O],1-hydroxyxanthen-9-one,3.8\nCOc1cc2c(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)ncnc2cc1OCCCN(CCO)CC(C)C,\"InChI=1S/C29H35F2N7O4/c1-18(2)16-38(9-10-39)8-5-11-42-25-15-23-20(14-24(25)41-3)29(33-17-32-23)35-26-12-19(36-37-26)13-27(40)34-22-7-4-6-21(30)28(22)31/h4,6-7,12,14-15,17-18,39H,5,8-11,13,16H2,1-3H3,(H,34,40)(H2,32,33,35,36,37)\",[C][O][C][=C][C][=C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][N][=C][N][=C][Ring2][Ring1][Branch2][C][=C][Ring2][Ring1][N][O][C][C][C][N][Branch1][Ring2][C][C][O][C][C][Branch1][C][C][C],\"n-(2,3-difluorophenyl)-2-[5-[[7-[3-(2-hydroxyethyl-(2-methylpropyl)amino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\",3.61\nCOc1cc2c(Nc3c(Cl)ccc4OCOc34)ncnc2cc1OCCCN5CCCCC5,\"InChI=1S/C24H27ClN4O4/c1-30-20-12-16-18(13-21(20)31-11-5-10-29-8-3-2-4-9-29)26-14-27-24(16)28-22-17(25)6-7-19-23(22)33-15-32-19/h6-7,12-14H,2-5,8-11,15H2,1H3,(H,26,27,28)\",[C][O][C][=C][C][=C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][N][=C][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C][C][C][N][C][C][C][C][C][Ring1][=Branch1],\"n-(5-chloro-1,3-benzodioxol-4-yl)-6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-amine\",2.05\nC(Cn1c2CCCCc2c3c(nc(nc13)N4CCCC4)N5CCCC5)N6CCOCC6,InChI=1S/C24H36N6O/c1-2-8-20-19(7-1)21-22(28-9-3-4-10-28)25-24(29-11-5-6-12-29)26-23(21)30(20)14-13-27-15-17-31-18-16-27/h1-18H2,[C][Branch2][Ring2][Branch2][C][N][C][C][C][C][C][C][=Ring1][=Branch1][C][=C][Branch2][Ring1][C][N][=C][Branch1][#Branch1][N][=C][Ring1][=N][Ring1][=Branch1][N][C][C][C][C][Ring1][Branch1][N][C][C][C][C][Ring1][Branch1][N][C][C][O][C][C][Ring1][=Branch1],\"9-(2-morpholin-4-ylethyl)-2,4-dipyrrolidin-1-yl-5,6,7,8-tetrahydropyrimido[6,5-b]indole\",3.6\nCC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccs2)N)C(=O)C(F)(F)F,\"InChI=1S/C16H17F3N4O3S/c1-8(2)12(13(25)16(17,18)19)22-11(24)7-23-14(10-4-3-5-27-10)21-6-9(20)15(23)26/h3-6,8,12H,7,20H2,1-2H3,(H,22,24)\",[C][C][Branch1][C][C][C][Branch2][Ring1][N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=N][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F],\"2-(5-amino-6-oxo-2-thiophen-2-ylpyrimidin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\",0.68\nCc1ccnc2nc(nn12)C(=O)Nc3nccs3,\"InChI=1S/C10H8N6OS/c1-6-2-3-11-9-13-7(15-16(6)9)8(17)14-10-12-4-5-18-10/h2-5H,1H3,(H,12,14,17)\",[C][C][=C][C][=N][C][=N][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1],\"7-methyl-n-(1,3-thiazol-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidine-2-carboxamide\",0.31\nCCCCC(CC)COC(=O)CC(C(=O)OCC(CC)CCCC)S(=O)(=O)O,\"InChI=1S/C20H38O7S/c1-5-9-11-16(7-3)14-26-19(21)13-18(28(23,24)25)20(22)27-15-17(8-4)12-10-6-2/h16-18H,5-15H2,1-4H3,(H,23,24,25)\",[C][C][C][C][C][Branch1][Ring1][C][C][C][O][C][=Branch1][C][=O][C][C][Branch1][S][C][=Branch1][C][=O][O][C][C][Branch1][Ring1][C][C][C][C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][O],\"1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonic acid\",2.93\nCN1CCCC1CCOC(C)(c2ccccc2)c3ccc(Cl)cc3,\"InChI=1S/C21H26ClNO/c1-21(17-7-4-3-5-8-17,18-10-12-19(22)13-11-18)24-16-14-20-9-6-15-23(20)2/h3-5,7-8,10-13,20H,6,9,14-16H2,1-2H3\",[C][N][C][C][C][C][Ring1][Branch1][C][C][O][C][Branch1][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],2-[2-[1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine,3.04\nNC1=NC(CC(=O)N1)c2ccc(Cl)c(Cl)c2,\"InChI=1S/C10H9Cl2N3O/c11-6-2-1-5(3-7(6)12)8-4-9(16)15-10(13)14-8/h1-3,8H,4H2,(H3,13,14,15,16)\",[N][C][=N][C][Branch1][=Branch2][C][C][=Branch1][C][=O][N][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2],\"2-amino-6-(3,4-dichlorophenyl)-5,6-dihydro-3h-pyrimidin-4-one\",1.46\nNCC(O)(c1ccc(Cl)cc1)c2ccc(Cl)cc2,\"InChI=1S/C14H13Cl2NO/c15-12-5-1-10(2-6-12)14(18,9-17)11-3-7-13(16)8-4-11/h1-8,18H,9,17H2\",[N][C][C][Branch1][C][O][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1],\"2-amino-1,1-bis(4-chlorophenyl)ethanol\",2.69\nCc1ccnc(NS(=O)(=O)c2ccc(N)cc2)n1,\"InChI=1S/C11H12N4O2S/c1-8-6-7-13-11(14-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15)\",[C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][=N][Ring1][P],4-amino-n-(4-methylpyrimidin-2-yl)benzenesulfonamide,-0.51\nO[C@@H](CNCCOCCCNCCc1cccc(Cl)c1)c2ccc(O)c3NC(=O)Sc23,\"InChI=1S/C22H28ClN3O4S/c23-16-4-1-3-15(13-16)7-9-24-8-2-11-30-12-10-25-14-19(28)17-5-6-18(27)20-21(17)31-22(29)26-20/h1,3-6,13,19,24-25,27-28H,2,7-12,14H2,(H,26,29)/t19-/m0/s1\",[O][C@@H1][Branch2][Ring1][#Branch1][C][N][C][C][O][C][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1],\"7-[(1r)-2-[2-[3-[2-(3-chlorophenyl)ethylamino]propoxy]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\",0.83\nCN1CCC[C@@H]([C@H]1C(=O)Nc2ccc(OCc3cc(C)nc4ccccc34)cc2)C(=O)NO,\"InChI=1S/C25H28N4O4/c1-16-14-17(20-6-3-4-8-22(20)26-16)15-33-19-11-9-18(10-12-19)27-25(31)23-21(24(30)28-32)7-5-13-29(23)2/h3-4,6,8-12,14,21,23,32H,5,7,13,15H2,1-2H3,(H,27,31)(H,28,30)/t21-,23-/m0/s1\",[C][N][C][C][C][C@@H1][Branch2][Ring2][Branch2][C@H1][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring1][Ring2][O][C][C][=C][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][N][O],\"(2s,3s)-n'-hydroxy-1-methyl-n-[4-[(2-methylquinolin-4-yl)methoxy]phenyl]piperidine-2,3-dicarboxamide\",2.41\nCOC(=O)COc1ccc(cn1)C(=O)Nc2ccc(F)cc2,\"InChI=1S/C15H13FN2O4/c1-21-14(19)9-22-13-7-2-10(8-17-13)15(20)18-12-5-3-11(16)4-6-12/h2-8H,9H2,1H3,(H,18,20)\",[C][O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1],methyl 2-[5-[(4-fluorophenyl)carbamoyl]pyridin-2-yl]oxyacetate,2.43\nCc1cccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)c1,\"InChI=1S/C19H20N6O3/c1-13-3-2-4-14(11-13)22-19-24-23-18(28-19)17(26)21-15-5-6-16(20-12-15)25-7-9-27-10-8-25/h2-6,11-12H,7-10H2,1H3,(H,21,26)(H,22,24)\",[C][C][=C][C][=C][C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][O],\"5-[(3-methylphenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\",3.42\nCCN(C1CCN(CCC(c2ccc(F)cc2)c3ccc(F)cc3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C,\"InChI=1S/C31H36F2N2O3S/c1-3-35(31(36)22-23-4-14-29(15-5-23)39(2,37)38)28-16-19-34(20-17-28)21-18-30(24-6-10-26(32)11-7-24)25-8-12-27(33)13-9-25/h4-15,28,30H,3,16-22H2,1-2H3\",[C][C][N][Branch2][Ring2][Branch2][C][C][C][N][Branch2][Ring1][N][C][C][C][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C],\"n-[1-[3,3-bis(4-fluorophenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide\",3.21\nCOc1cccc2[nH]ncc12,\"InChI=1S/C8H8N2O/c1-11-8-4-2-3-7-6(8)5-9-10-7/h2-5H,1H3,(H,9,10)\",[C][O][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1],4-methoxy-1h-indazole,2.1\nClc1ccc2ncccc2c1C(=O)NCC3CCCCC3,\"InChI=1S/C17H19ClN2O/c18-14-8-9-15-13(7-4-10-19-15)16(14)17(21)20-11-12-5-2-1-3-6-12/h4,7-10,12H,1-3,5-6,11H2,(H,20,21)\",[Cl][C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Ring1][=Branch1],6-chloro-n-(cyclohexylmethyl)quinoline-5-carboxamide,2.65\n"
  },
  {
    "path": "dataset/chembl/chembl.json",
    "content": "[\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][=Branch2][C][C][C][N][Branch2][Ring1][=N][C][C][C][Branch1][S][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" berry\\n\",\n        \"output\": \" berry is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H28N2O3/c1-3-26(4-2)23(28)18-10-8-17(9-11-18)19-16-24(12-14-25-15-13-24)29-21-7-5-6-20(27)22(19)21/h5-11,16,25,27H,3-4,12-15H2,1-2H3\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" argentina\\n\",\n        \"output\": \" argentina is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Branch1][Ring1][C][=O][C][=C][Branch1][C][O][C][=Branch1][O][=C][Branch1][C][C][C][=C][Ring1][S][Ring1][Branch2][C][=C][Branch1][C][C][C][=C][C][Branch1][=Branch1][C][Branch1][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Branch1][Ring1][C][=O][C][Ring1][=N][=C][Ring2][Ring1][C][O]\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=N][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1cc(nc2ccc(Nc3cc(nc(N)n3)c4ccc(cc4)C(F)(F)F)cc12)c5ccc(F)cc5\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][S][C][=C][O][C][C][O][C][=Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(methylsulfamoylamino)-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H29NO5/c1-7-22(23(2)3,17-11-9-8-10-12-17)15-28-21(24)16-13-18(25-4)20(27-6)19(14-16)26-5/h8-14H,7,15H2,1-6H3\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-butyl-n-[2-[[(2r)-2-hydroxy-2-(4-hydroxy-2-oxo-3h-1,3-benzothiazol-7-yl)ethyl]amino]ethyl]-3-(2-phenylethoxy)propanamide\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-chloro-n-(5-phenyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" c1ccc(cc1)c2nnc(s2)c3ccccc3\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccccc1N2C(=Nc3cccc(C)c3C2=O)Cn4cnc5c(N)ncnc45\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3/t16-/m0/s1\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][N][Branch1][Ring1][C][=O][C][Branch2][Ring1][=C][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][O][C][C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=C][Branch1][=Branch2][C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][S][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-[(1r)-1-hydroxy-2-methylaminoethyl]benzamide\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=N][C][C][N][Ring1][Branch1]\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H24ClN3O/c1-3-21(4-2)10-6-8-19-12-13-11-15(18)14-7-5-9-20-16(14)17(13)22/h5,7,9,11,19,22H,3-4,6,8,10,12H2,1-2H3\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c(SCCCO)n(Cc3cccc4ccccc34)cc12\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc(cc1)[N+](=O)[O-]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H20N2O2/c1-10(2)16-8-11(17)9-18-14-5-3-4-13-12(14)6-7-15-13/h3-7,10-11,15-17H,8-9H2,1-2H3\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-amino-3-methyl-6-(2-phenylethyl)pyrimidin-4-one\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][S][C][=N][C][=N][C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][=C][Ring2][Ring1][#Branch1][C][=Ring2][Ring1][#Branch2][C]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H19ClN4O5/c1-32-8-7-24-20(29)13-4-2-3-12(9-13)11-27-22(31)17-18(21(30)26-27)25-16-10-14(23)5-6-15(16)19(17)28/h2-6,9-10H,7-8,11H2,1H3,(H,24,29)(H,25,28)(H,26,30)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[2-[[3,5-bis(trifluoromethyl)phenyl]methoxy]-1-phenylethyl]piperazine\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(5,6-dimethylthieno[3,2-e]pyrimidin-4-yl)sulfanyl-1-pyrrolidin-1-ylethanone\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H28N4O2/c1-24-12-14-25(15-13-24)20(17-8-10-19(27-2)11-9-17)16-22-21(26)23-18-6-4-3-5-7-18/h3-11,20H,12-16H2,1-2H3,(H2,22,23,26)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Ring2][C][C][=C][C][=C][Branch1][C][C][N][Branch1][C][C][N][=C][Ring1][#Branch1][C][=Ring1][O][C][=C][C][=N][C][Branch2][Ring1][#Branch1][N][C][=C][C][=C][Branch1][C][C][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][Ring2][Ring1][C]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" pyridin-3-ylmethyl n-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][=C][C][Branch1][C][Cl][=C][Branch1][C][O][C][=C][Ring1][Branch2][C@H1][Branch1][Ring2][C][Ring1][=N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc(cc1)N2C(=O)c3ccccc3C2=O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [6-hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl]-[4-(2-piperidin-1-ylethoxy)phenyl]methanone\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H20F3N3O4/c1-12(2)17(18(29)20(21,22)23)25-16(28)10-26-15(13-6-4-3-5-7-13)9-8-14(19(26)30)24-11-27/h3-9,11-12,17H,10H2,1-2H3,(H,24,27)(H,25,28)\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][N][=C][N][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][O][C][C][C][N][C][C][C][C][C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch1][O][C][Branch1][C][C][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H16ClN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][S+1][Branch1][C][O-1][C][=C][C][=C][Branch2][Ring1][=C][\\\\C][=C][\\\\C][=Branch2][Ring1][#Branch1][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][F][=C][C][=C][/-Ring1][=C][Ring1][#Branch1][C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1Nc2ccccc2C=C1\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C33H35NO6S/c1-20(2)25-11-7-6-10-21(25)18-22-19-26(30(36)31(37)29(22)35)32(38)34-23-14-16-24(17-15-23)41(39,40)28-13-9-8-12-27(28)33(3,4)5/h6-17,19-20,35-37H,18H2,1-5H3,(H,34,38)\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" S=C(NC1CCCCC1)N2CCC(CC2)c3cnc[nH]3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H22FN3O3/c23-17-7-5-15(6-8-17)20(27)16-9-11-25(12-10-16)13-14-26-21(28)18-3-1-2-4-19(18)24-22(26)29/h1-8,16H,9-14H2,(H,24,29)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H7ClF2N2O/c13-11-4-2-8(6-16-11)17-12(18)7-1-3-9(14)10(15)5-7/h1-6H,(H,17,18)\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n'-(5-cyclopropyl-1h-pyrazol-3-yl)-5-fluoro-n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H42N4O2/c1-20(28-2)26(32)29-25(23-11-7-4-8-12-23)27(33)31-18-15-22-14-17-30(19-24(22)31)16-13-21-9-5-3-6-10-21/h3,5-6,9-10,20,22-25,28H,4,7-8,11-19H2,1-2H3,(H,29,32)/t20-,22+,24+,25-/m0/s1\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC[C@H](N1CCN(C[C@@H]1C)C2(C)CCN(CC2)C(=O)c3c(C)ncnc3C)c4ccc(cc4)C(F)(F)F\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1s,2r,3r,5r)-3-(hydroxymethyl)-5-[7-[[(1r,2s)-2-phenylcyclopropyl]amino]-5-propylsulfanyltriazolo[5,4-d]pyrimidin-3-yl]cyclopentane-1,2-diol\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-phenylpiperazin-1-yl)propane-1,2-diol\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-chloro-n-(2,5-difluorophenyl)benzenesulfonamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 10-ethyl-3-methylpyrimido[6,5-b]quinoline-2,4-dione\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" pyrido[2,1-b]pyrimidin-4-one\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H22ClFN4O2/c1-28-19-12-18-15(11-20(19)29-9-8-27-6-2-3-7-27)21(25-13-24-18)26-14-4-5-17(23)16(22)10-14/h4-5,10-13H,2-3,6-9H2,1H3,(H,24,25,26)\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-dimethyl-2-[(2-methylphenyl)-phenylmethoxy]ethanamine\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][C][C@H1][Branch1][Ring2][C][Ring1][Branch1][O][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C]\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2ncc(C)c(Nc3ccccc3)n2)cc1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-fluoro-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)-4-oxo-1h-quinoline-2-carboxamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(phenoxy)-n-(pyridin-4-ylmethyl)benzamide\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H9N3/c11-10-6-9(12-7-13-10)8-4-2-1-3-5-8/h1-7H,(H2,11,12,13)\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H15N3O2S/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H24N8O2S/c1-28(2)14-4-12-25-32(30,31)17-8-6-16(7-9-17)26-21-22-13-10-18(27-21)19-15-23-20-5-3-11-24-29(19)20/h3,5-11,13,15,25H,4,12,14H2,1-2H3,(H,22,26,27)\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][P][=N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C][Ring1][O][=O][C][N][C][=N][C][=C][Branch1][C][N][N][=C][N][=C][Ring1][#Branch2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccccc1CNC(=O)c2ccc3cnccc3n2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)N1c2ccccc2C=Cc3ccccc13\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][C][C][\\\\N][=C][/C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][\\\\-Ring2][Ring1][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1cccc(Nc2ncnc3ccccc23)c1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[2-[4-(4-fluorobenzoyl)piperidin-1-yl]ethyl]-1h-quinazoline-2,4-dione\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][Branch1][C][N][=C][C][=C][Ring1][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2cccc(c2)C(=O)O)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C@H1][Branch1][P][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H21NO4/c1-11(6-12-2-4-14(19)5-3-12)18-10-17(22)13-7-15(20)9-16(21)8-13/h2-5,7-9,11,17-22H,6,10H2,1H3\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][N][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#C]\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (8s,9r,10s,11s,13s,14s,16r,17r)-9-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][O][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][Branch2][=N][C][=C][Ring2][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch2][=Branch1][O][N][C][=C][C][=C][Branch2][Ring2][N][N][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring2][Ring1][=Branch2][=Ring1][N][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring2][Ring2][#Branch2][=Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H19F3N2O4S/c1-29-19-6-2-3-7-20(19)30-18-10-8-17(9-11-18)26(14-16-5-4-12-25-13-16)31(27,28)15-21(22,23)24/h2-13H,14-15H2,1H3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][C][C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][Branch1][C][C][C][Ring1][=Branch2][=O][C][Branch1][O][C][C][C][C][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14N2O/c1-2-6-13(7-3-1)18-10-12-11-19-15-9-5-4-8-14(15)16(12)17-18/h1-9,12H,10-11H2\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" methyl 2-[3-[[6-amino-2-(2-methoxyethoxy)-8-oxo-7h-purin-9-yl]methyl]phenyl]acetate\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccsc1C(=CCCN2CCC[C@H](C2)C(=O)O)c3sccc3C\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(3-chlorophenyl)-n-(oxan-4-yl)imidazo[2,1-f]pyridazin-6-amine\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)COc1ccc(Br)cc1c2ccccc2\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H23N3O3/c27-22(19-8-3-6-17-5-1-2-7-18(17)19)26-20-9-4-12-24-21(20)23(28)25-15-16-10-13-29-14-11-16/h1-9,12,16H,10-11,13-15H2,(H,25,28)(H,26,27)\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(ccc1Cc2c[nH]c3ccc(NC(=O)CC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5C\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C=CCCCCCCCCC(=O)N[C@H]1CCC(=O)NC1=O\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][#C][C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][Ring2][Ring1][Ring2][=O]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-oxo-2-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]amino]ethyl]benzoic acid\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4,6-dimethylpyrimidin-2-yl)sulfanylacetamide\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(NC1CCCCC1)c2cccnc2Sc3ccccc3\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][Branch1][C][F][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][C][=C][Branch1][Branch1][O][N][=Ring1][Branch1][N][Branch1][=N][C][C][C][N][C][C][C][C][C][C][Ring1][#Branch1][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1cc(Nc2ncnc3[nH]nc(OCCN4CCCC4)c23)ccc1OCc5ccccn5\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=N][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCCC(CC1)N2N=C(Cc3ccc(Cl)cc3)c4ccccc4C2=O\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][N][C][C][C][C][N][C][C][C][C][Ring1][Branch1][S][N][=C][Ring2][Ring1][C][O][C][C][=C][Branch1][C][F][C][=C][Branch1][C][Br][C][=C][Ring1][Branch2][F]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C36H47N5O4/c1-36(2,3)39-35(45)31-24-40(22-26-12-9-15-37-21-26)16-17-41(31)23-29(42)19-28(18-25-10-5-4-6-11-25)34(44)38-33-30-14-8-7-13-27(30)20-32(33)43/h4-15,21,28-29,31-33,42-43H,16-20,22-24H2,1-3H3,(H,38,44)(H,39,45)/t28-,29+,31+,32-,33+/m1/s1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H16F6N6O/c1-36-19-7-6-15(10-17(19)34-22(36)33-14-4-2-13(3-5-14)23(25,26)27)37-16-8-9-31-18(11-16)21-32-12-20(35-21)24(28,29)30/h2-12H,1H3,(H,32,35)(H,33,34)\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" phenyl-pyridin-3-ylmethanol\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][N][Branch2][Ring1][N][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1][C][=Branch1][C][=O][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][=C][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][=C][Branch1][C][F][C][=C][Ring1][=N][C][Ring2][Ring1][Ring2][=O]\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[4-[(2-pyridin-2-ylethylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" -0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H11N3O3S/c1-9-4-2-5-10(8-9)16-20(17,18)12-7-3-6-11-13(12)15-19-14-11/h2-8,16H,1H3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5,7-dihydroxy-3-(4-methoxyphenyl)chromen-4-one\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CS(=O)(=O)Cc1cc(nc(n1)c2ccccc2)N3CCOCC3\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r,3r,4s,5r)-2-(2-amino-6-methoxypurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1cccc2c1c(Oc3ccc(Cl)cc3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(CCCc1ccccc1)S(=O)(=O)c2cc(C(=O)N3CCc4ccc(cc4C3)S(=O)(=O)NCCc5ccccc5)c(O)c(O)c2O\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)C(=O)N4CCCN(C)CC4)ncc2F\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-nitrophenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[4-(2-morpholin-4-ylethoxy)naphthalen-1-yl]urea\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 4-[2-[1-(6-methylpyridazin-3-yl)piperidin-4-yl]ethoxy]benzoate\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[[5-chloro-4-(phenylamino)pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-chloro-2-methyl-n-[4-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-1,3-thiazol-2-yl]benzenesulfonamide\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H32N2O2/c1-23(21(25)16-18-8-3-2-4-9-18)19-10-12-22(11-7-15-26-22)17-20(19)24-13-5-6-14-24/h2-4,8-9,19-20H,5-7,10-17H2,1H3/t19-,20-,22-/m0/s1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][C][C][C][Branch1][Ring2][N][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][=Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][N][=C][C][=C][C][Branch1][#Branch2][N][C][C][C][O][C][C][Ring1][=Branch1][=N][N][Ring1][S][Ring1][=N]\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (3s,4r)-3-(1,3-benzodioxol-5-yloxymethyl)-4-(4-fluorophenyl)piperidine\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(benzoyl)-3-methyl-1,3-dihydroquinoxalin-2-one\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-n-(5,6-dimethoxypyrimidin-4-yl)benzenesulfonamide\\n\",\n        \"output\": \" -0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5-bromo-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-phenyl-1,3-thiazol-2-amine\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" save\\n\",\n        \"output\": \" save is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[4,5-di(phenyl)-1,3-oxazol-2-yl]propanoic acid\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (9z)-n,n-dimethyl-9-[3-(4-methylpiperazin-1-yl)propylidene]thioxanthene-2-sulfonamide\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-chlorophenyl)pyridine-2-carboxamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14ClN3O2/c1-2-4-14(21)19-10-6-7-12(17)11(9-10)16-20-15-13(22-16)5-3-8-18-15/h3,5-9H,2,4H2,1H3,(H,19,21)\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch1][O][C][=C][N][C][=Branch1][C][=S][N][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-[[(2r)-1-hydroxybutan-2-yl]amino]-5-(phenylmethylsulfanyl)-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1]\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)N1C(=O)N(C)C(=O)c2cn(Cc3cccc4ccccc34)cc12\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=N][C][S][C][=C][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][C][C][Branch2][Ring1][Branch1][C][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring1][=N][C][=Branch1][C][=O][C][=Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][Branch2][O][C]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1N(C(=Nc2c1cnn2c3ccccc3)c4occc4)c5ccccc5\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H8ClN3O/c13-9-4-3-7(14)6-8(9)12-16-11-10(17-12)2-1-5-15-11/h1-6H,14H2\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][Branch1][O][N][=C][Ring1][=Branch1][N][C][Branch1][C][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H31ClN2O/c24-21-2-1-19(18-3-5-25-6-4-18)10-20(21)22(27)26-14-23-11-15-7-16(12-23)9-17(8-15)13-23/h1-2,10,15-18,25H,3-9,11-14H2,(H,26,27)\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][O][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][N][=Ring1][N]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 9-butyl-8-[(3,4,5-trimethoxyphenyl)methyl]purin-6-amine\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1cccc(c1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" methyl 3-[2-(1,3-benzodioxol-5-ylmethylamino)-2-oxoethyl]-4-(2-imidazol-1-ylpyrimidin-4-yl)piperazine-1-carboxylate\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][C][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring2]\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-bromo-n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2,3-dimethoxybenzamide\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H23NO5/c1-29-21(26)11-5-3-2-4-10-20(25)24-15-12-13-17-16-8-6-7-9-18(16)22(27)23(28)19(17)14-15/h6-9,12-14H,2-5,10-11H2,1H3,(H,24,25)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC[C@@H](O)CN1C(=O)C=NN(C1=O)c2ccc(Cl)c(c2)C(=O)NCC3(O)CCCCCC3\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOc1ccc(cc1)N2C(=O)c3ccccc3N=C2[C@@H](C)N(Cc4cccnc4)C(=O)Cc5ccc(cc5)C(F)(F)F\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][C][=C][Branch2][Ring1][C][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13)\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-chloro-2-(thiophen-2-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H17NO3/c1-4-16(5-2)12-7-6-11-8-13(10(3)17)15(18)19-14(11)9-12/h6-9H,4-5H2,1-3H3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-aminophenyl)-4-[[(4-pyridin-3-ylpyrimidin-2-yl)amino]methyl]benzamide\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H15BrFNO3S/c17-13-3-7-15(8-4-13)23(21,22)10-9-16(20)19-11-12-1-5-14(18)6-2-12/h1-8H,9-11H2,(H,19,20)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][C][C][C][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1h-quinolin-2-one\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2nccc(Nc3cc(C)ccc3F)n2)cc1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=Branch1][=N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H23F3N2O2/c1-26-18-10-9-16(27-20(21,22)23)12-15(18)13-25-17-8-5-11-24-19(17)14-6-3-2-4-7-14/h2-4,6-7,9-10,12,17,19,24-25H,5,8,11,13H2,1H3/t17-,19-/m0/s1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C1Cc2ncc(c3ccc4OCCOc4c3)n2C1\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-indol-1-ylpyrimidin-2-amine\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H24N2O5/c1-29-21-12-16(22(26)27)6-7-17(21)14-25-11-10-15-8-9-18(13-20(15)25)24-23(28)30-19-4-2-3-5-19/h6-13,19H,2-5,14H2,1H3,(H,24,28)(H,26,27)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H13N3O2S/c1-15-11(17)9-7-10(8-5-3-2-4-6-8)19-12(9)16-13(14)18/h2-7H,1H3,(H,15,17)(H3,14,16,18)\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(CC2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Ring1][=Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][N][=N][C][=Branch1][Ring2][=N][Ring1][Branch1][C][=C][C][=C][C][Branch1][P][O][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C@@H1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1][C][Ring1][P]\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)C(=O)NC4CCN(C)CC4)ncc2F\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[2-[2-(5-amino-1,3,4-thiadiazol-2-yl)ethylsulfanyl]ethyl]-1,3,4-thiadiazol-2-amine\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)COc1ccc(Cl)cc1CN2CCCN(CC2)S(=O)(=O)Cc3ccccc3\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H20N2O2/c1-12-2-4-14(5-3-12)19-15(18)17-11-10-16-8-6-13(17)7-9-16/h2-5,13H,6-11H2,1H3\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4ccccn4)C3=O\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(3-hydroxyphenyl)-1,3-benzothiazol-6-ol\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][Branch2][Ring2][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring2][Ring1][=C][O]\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1cc(ccc1C2=CCS(=O)(=O)CC2)N3C[C@H](Cn4nncc4F)OC3=O\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(3-formamido-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][C][N][Branch1][Ring2][C][Ring1][Branch1][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H25NO6/c1-12(24)23-16-8-6-13-10-19(27-3)21(28-4)22(29-5)20(13)14-7-9-18(26-2)17(25)11-15(14)16/h7,9-11,16H,6,8H2,1-5H3,(H,23,24)/t16-/m0/s1\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-amino-n-(4-methoxyphenyl)pyrimidine-4-carboxamide\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1CC(CC(C)(C)C1)OC(=O)C(O)c2ccccc2\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Ring1][C@H1][Branch1][C][O][C@H1][C][C@@H1][C][C][N][Ring1][=Branch1][C][C@@H1][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(C1CCN(CCC(c2ccc(F)cc2)c3ccc(F)cc3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" furan-2-yl-[4-[4-(4-methylphenyl)phthalazin-1-yl]piperazin-1-yl]methanone\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (1s,3s)-n'-(7-methoxy-4-methylquinolin-2-yl)-n-[[3-(trifluoromethoxy)phenyl]methyl]cyclohexane-1,3-diamine\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][=C][Branch2][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][#Branch1][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H18ClN3O3S/c1-12-18-14(10-16(19-12)20-6-8-23-9-7-20)11-24(21,22)15-4-2-13(17)3-5-15/h2-5,10H,6-9,11H2,1H3\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[[3-(phenoxy)phenyl]methyl]-1,3-thiazolidine-2,4-dione\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C@H1][Branch1][C][O][C][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1sc2CCCCc2c1C(=O)NCc3ccccc3\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H11N3O/c15-14-16-11-8-4-5-9-12(11)17(14)13(18)10-6-2-1-3-7-10/h1-9H,(H2,15,16)\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Ring1][O][C][C][=Branch1][Ring2][=C][Ring1][Branch2][C][Branch1][C][O][C][N][C][=Branch1][C][=O][C][N]\\n\",\n        \"output\": \" -0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H8N4/c10-8-3-5-12-9(13-8)7-2-1-4-11-6-7/h1-6H,(H2,10,12,13)\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H11N3O/c15-14-16-11-7-6-10(8-12(11)17-14)13(18)9-4-2-1-3-5-9/h1-8H,(H3,15,16,17)\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1ccc(cc1)C(=O)Nc2ccccc2N\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H21NO2/c21-18-7-3-15(4-8-18)14-1-5-16(6-2-14)19(22)13-20-11-9-17(19)10-12-20/h1-8,17,21-22H,9-13H2\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonic acid\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][P][N][C][=N][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=C][C][=Branch1][Ring2][=N][Ring1][=N][N][C][C][O][C][C][Ring1][=Branch1][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=N][S][C][=C][Branch1][C][C][N][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][Branch2][C][C][N][C][C][Ring1][=Branch1][O][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][S][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOC(=O)c1ccccc1c2csc(NS(=O)(=O)c3ccc(Cl)cc3)n2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C30H29N5O2/c1-20-29(36)33-28(27(31-20)22-7-3-2-4-8-22)23-13-11-21(12-14-23)19-34-17-15-24(16-18-34)35-26-10-6-5-9-25(26)32-30(35)37/h2-14,24H,15-19H2,1H3,(H,32,37)(H,33,36)\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12N2O2S/c1-19-12-8-4-2-6-10(12)14(18)17-15-16-11-7-3-5-9-13(11)20-15/h2-9H,1H3,(H,16,17,18)\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)n2cnc3cc(NS(=O)(=O)c4ccccc4)ccc23\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[4-[[2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-methylsulfonyl-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-5-(phenylmethoxycarbonylamino)pyridin-2-yl]benzoic acid\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ncc([N+](=O)[O-])n1CCO\\n\",\n        \"output\": \" -0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-(4-hydroxyphenyl)naphthalen-2-ol\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring1][#C]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H20N2OS/c21-18(15-22-17-9-5-2-6-10-17)20-13-11-19(12-14-20)16-7-3-1-4-8-16/h1-10H,11-15H2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-fluorophenyl)-5-(morpholin-4-ylmethyl)-4-phenylpyrazol-3-amine\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H22Cl2N4/c1-17(2)30-24-16-27-25(15-23(24)31-20-11-7-18(28)8-12-20)32-22-5-3-4-6-26(22)33(27)21-13-9-19(29)10-14-21/h3-17,31H,1-2H3\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C32H38N2O3S/c1-3-21-34(32(35)25-26-14-16-30(17-15-26)38(2,36)37)29-18-22-33(23-19-29)24-20-31(27-10-6-4-7-11-27)28-12-8-5-9-13-28/h3-17,29,31H,1,18-25H2,2H3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H12ClNO3/c1-9(16(19)20)11-4-7-14-13(8-11)18-15(21-14)10-2-5-12(17)6-3-10/h2-9H,1H3,(H,19,20)\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2,6-diethylphenyl)-3-[[4-(4-methylpiperazin-1-yl)benzoyl]amino]-4,6-dihydro-1h-pyrrolo[3,4-d]pyrazole-5-carboxamide\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1S(=O)(=O)c3ccccc3\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C]\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-(acetyl-ethylamino)-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=N][C][=C][C][=C][Branch1][#Branch2][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H30FN7O/c1-15(2)32-16(3)26-13-21(32)22-20(25)12-27-24(29-22)28-18-8-6-17(7-9-18)23(33)31-11-10-19(14-31)30(4)5/h6-9,12-13,15,19H,10-11,14H2,1-5H3,(H,27,28,29)/t19-/m0/s1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[3-(3,5-difluorophenoxy)-5-[(2s)-1-methoxypropan-2-yl]oxybenzoyl]amino]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1N2CCN(CCCCNC(=O)c3ccc4ccccc4c3)CC2\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring1][P][=O]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1F)c2cc(nn2c3ccc(cc3)S(=O)(=O)N)C(F)F\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][Branch1][C][O][C@@H1][Branch1][Ring1][C][F][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1C(=O)c2cccnc2c3ccccc13\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][C][C@@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H11N3/c1-2-6-11(7-3-1)17-14-12-8-4-5-9-13(12)15-10-16-14/h1-10H,(H,15,16,17)\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" pediatrician\\n\",\n        \"output\": \" pediatrician is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=N][N][C][=N][C][=C][Branch2][Ring1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][S][Ring1][S][N][=C][N][=C][Ring2][Ring1][#Branch1][C][=C][Ring2][Ring1][O][O][C][C][C][N][C][C][C][Branch1][Ring1][C][O][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)CC1(CC=C)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O[C@H](CNC(=O)C1=CNC(=O)c2ccccc12)CN3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H16N2O/c1-7-5-4-6-8(2)10(7)13-11(14)9(3)12/h4-6,9H,12H2,1-3H3,(H,13,14)\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][C][Branch1][=N][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H9N3OS/c1-7-9(15-13-12-7)10(14)11-8-5-3-2-4-6-8/h2-6H,1H3,(H,11,14)\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=C][N][Branch1][=Branch2][C][C][C][N][C][C][Ring1][=Branch1][C][=Ring1][O][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-methyl-n-(phenylmethyl)quinolin-2-amine\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" dolphin\\n\",\n        \"output\": \" dolphin is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H23ClFNO2/c22-18-7-5-17(6-8-18)21(26)11-14-24(15-12-21)13-1-2-20(25)16-3-9-19(23)10-4-16/h3-10,26H,1-2,11-15H2\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)c2cc3cc(Cl)ccc3[nH]2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(e)-1-(4-methylphenyl)-3-pyrrolidin-1-ylprop-1-enyl]pyridine\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H17N3O4S/c1-9-15(10(2)24-20-9)16(21)19-17-18-12(8-25-17)11-5-6-13(22-3)14(7-11)23-4/h5-8H,1-4H3,(H,18,19,21)\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H25F3N4O5/c1-16(2)22(23(35)26(27,28)29)32-21(34)14-33-20(18-6-4-3-5-7-18)9-8-19(24(33)36)31-25(37)38-15-17-10-12-30-13-11-17/h3-13,16,22H,14-15H2,1-2H3,(H,31,37)(H,32,34)\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)C1=C(C)N(C)N(C1=O)c2ccccc2\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][N][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H13F4NO4S/c1-15(23,16(18,19)20)14(22)21-11-4-8-13(9-5-11)26(24,25)12-6-2-10(17)3-7-12/h2-9,23H,1H3,(H,21,22)\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenoxy)-5-fluoro-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n,n-bis(phenylmethyl)-2h-tetrazol-5-amine\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C@H1][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][C@H1][Ring1][Branch1][C][C@H1][Ring1][Branch2][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@@H1][Branch2][Ring2][=C][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][#Branch2][N][C][=C][C][=C][C][Branch1][#C][C][=N][N][Ring1][Branch1][C][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring1][S][=C][Ring2][Ring1][O][Ring2][Ring1][#Branch1][C][=Branch1][C][=O][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1N2CCN(CCN(C(=O)C3CCCCC3)c4ccccn4)CC2\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H21NO2/c1-18-13-12-15(14-8-4-3-5-9-14)20-17-11-7-6-10-16(17)19-2/h3-11,15,18H,12-13H2,1-2H3\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(1-adamantyl)-n-(5-methoxy-2-methylphenyl)acetamide\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-(2-phenylethenyl)-2h-tetrazole\\n5-[(e)-2-phenylethenyl]-2h-tetrazole\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)NNC(=O)c1ccncc1\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(Nc1ccccc1)C2=CC(=CN3C(=O)C=C(N=C23)N4CCOCC4)C\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H15NO/c20-18(19-16-10-2-1-3-11-16)13-15-9-6-8-14-7-4-5-12-17(14)15/h1-12H,13H2,(H,19,20)\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(Cc2ccc(cc2)C(=O)Nc3ccc(C)c(Nc4nccc(n4)c5cccnc5)c3)CC1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][Branch2][Ring1][N][N][C][=C][C][=N][C][Branch1][P][N][C][C][O][N][=C][Branch1][Ring2][C][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][=N][NH1][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" vessel\\n\",\n        \"output\": \" vessel is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2-methylamino-1,3-thiazol-5-yl)-phenylmethanone\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(phenylmethyl)-1h-benzimidazol-2-amine\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(CNC(=O)Nc2ncc(s2)[N+](=O)[O-])cc1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H18ClFN6/c26-16-3-1-2-15(10-16)23-13-24(33-25(29)32-23)30-18-8-9-21-19(11-18)20(28)12-22(31-21)14-4-6-17(27)7-5-14/h1-13H,(H2,28,31)(H3,29,30,32,33)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccc(cc1)C2=Cc3ccccc3OC2=O\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-methoxybenzamide\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(4-fluorophenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10N4/c13-12-14-7-5-11(15-12)16-8-6-9-3-1-2-4-10(9)16/h1-8H,(H2,13,14,15)\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc2[nH]ccc2c1\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H12O5/c1-7-9-3-2-8(14)6-11(9)18-13(17)10(7)4-5-12(15)16/h2-3,6,14H,4-5H2,1H3,(H,15,16)\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(C)c(OCCCC(C)(C)C(=O)O)c1\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch2][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring2][Ring1][Ring2][Cl]\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-nitro-1h-indazole\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1cc(ccc1Cl)C2(O)NC(=O)c3ccccc23\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H19F6NO/c21-19(22,23)15-9-13(10-16(11-15)20(24,25)26)12-28-17-7-4-8-27-18(17)14-5-2-1-3-6-14/h1-3,5-6,9-11,17-18,27H,4,7-8,12H2/t17-,18-/m0/s1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n'-bis(phenylmethyl)ethane-1,2-diamine\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[4-(furan-2-carbonyl)piperazin-1-yl]-2-[(4,7,8-trimethyl-[1,2,4]triazolo[4,5-a]quinolin-1-yl)sulfanyl]ethanone\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H17ClN2O3/c21-13-5-6-16-12(7-13)9-18(22-16)20(26)23-17-8-11-3-1-2-4-14(11)15(17)10-19(24)25/h1-7,9,15,17,22H,8,10H2,(H,23,26)(H,24,25)/t15-,17-/m1/s1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OCC(=O)N1CCC(CC1)c2[nH]nc(c3ccc(Cl)cc3F)c2c4ccncn4\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" crib\\n\",\n        \"output\": \" crib is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H27N3O5S/c1-15(2)13-29-24-20(22(31)27(3)26(29)33)21(23(32)28-12-11-17(30)14-28)25(35-24)34-19-10-6-8-16-7-4-5-9-18(16)19/h4-10,15,17,30H,11-14H2,1-3H3/t17-/m1/s1\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN4CCCC4\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-methyl-2-phenyl-n-[(5r,7s,8s)-7-pyrrolidin-1-yl-1-oxaspiro[4.5]decan-8-yl]acetamide\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H31NO3/c1-3-21(4-2)14-15-23-16-17-24-19(22)20(12-8-9-13-20)18-10-6-5-7-11-18/h5-7,10-11H,3-4,8-9,12-17H2,1-2H3\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][Ring1][P][O][C]\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch2][Ring1][C][C][C][C][=Branch1][C][=O][N][Ring1][=Branch1][C][C][=C][C][=C][S][Ring1][Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-chlorophenyl)-1-[4-(2-diethylaminoethoxy)phenyl]-1-(4-methylphenyl)ethanol\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][O][C][=N][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][O][C][N][C][=Branch1][C][=O][C][S][C][=N][C][Branch1][C][C][=C][C][Branch1][C][C][=C][Ring1][Branch2][C][=Ring1][O][N][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[1-[1-[(2-methylphenyl)methyl]piperidin-4-yl]piperidin-4-yl]-1h-benzimidazol-2-one\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H24N4O2S2/c1-11(2)9-14(10-24)20-16-15-17(23-19(25)27-15)22-18(21-16)26-12(3)13-7-5-4-6-8-13/h4-8,11-12,14,24H,9-10H2,1-3H3,(H2,20,21,22,23,25)/t12-,14+/m0/s1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C37H45Cl2N2O2/c1-28(2)43-32-11-6-8-29(24-32)25-35(42)40-19-7-14-37(27-40,31-12-13-33(38)34(39)26-31)18-23-41-20-15-36(16-21-41,17-22-41)30-9-4-3-5-10-30/h3-6,8-13,24,26,28H,7,14-23,25,27H2,1-2H3/q+1/t36?,37-,41?/m1/s1\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[[3-methoxy-4-[(4-methoxyphenyl)methoxy]phenyl]methyl]pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-morpholin-4-yl-n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]acetamide\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][N][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][N][=C][N][=C][Ring2][Ring1][C][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H28N8OS/c1-15-13-20(29-28-15)25-19-14-21(31-11-9-30(2)10-12-31)27-23(26-19)33-18-7-5-17(6-8-18)24-22(32)16-3-4-16/h5-8,13-14,16H,3-4,9-12H2,1-2H3,(H,24,32)(H2,25,26,27,28,29)\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H11F3N2O3/c1-6(2)10(17)15-7-3-4-9(16(18)19)8(5-7)11(12,13)14/h3-6H,1-2H3,(H,15,17)\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3-chloro-2-fluorophenyl)-7-methoxy-6-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H23N3O4S/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21)/t11-/m0/s1\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Branch1][C][O][C][Ring1][#Branch1][=N][Ring1][O]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][N][C][=Branch1][C][=O][N][C@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N][C@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=O]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H22N2/c1-19-13-6-14-20-17-9-4-2-7-15(17)11-12-16-8-3-5-10-18(16)20/h2-5,7-10,19H,6,11-14H2,1H3\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)C2(F)F\\n\",\n        \"output\": \" -1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(nc(n1)n2ccnc2)N3CCC[C@@H]3C(=O)NCCc4ccc5OCOc5c4\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H29ClN4O/c22-18-17(1-2-24-19(18)26-5-3-23-4-6-26)20(27)25-13-21-10-14-7-15(11-21)9-16(8-14)12-21/h1-2,14-16,23H,3-13H2,(H,25,27)\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1,2-benzoxazol-3-ylmethanesulfonimidic acid\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-(3,5-dimethoxyphenyl)pyrido[6,5-d]pyrimidine-2,7-diamine\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-[(4-phenylsulfonylpiperazin-1-yl)methyl]-4-(trifluoromethyl)phenoxy]acetic acid\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-methyl-3-phenyl-6-pyridin-4-yl-[1,2]oxazolo[4,5-c]pyridin-4-one\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H13N3/c11-10(12)13-6-5-8-3-1-2-4-9(8)7-13/h1-4H,5-7H2,(H3,11,12)\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](Nc1ncc(F)c(Nc2cc(C)[nH]n2)n1)c3ncc(F)cn3\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H22N4O2/c1-4-23-9-13-20-14-15(21(13)10-17(2,3)22)11-7-5-6-8-12(11)19-16(14)18/h5-8,22H,4,9-10H2,1-3H3,(H2,18,19)\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H24FN5O4/c1-11-7-15-16(27-11)5-6-17(19(15)23)32-21-20-13(3)18(8-28(20)26-10-25-21)30-9-12(2)31-22(29)14(4)24/h5-8,10,12,14,27H,9,24H2,1-4H3/t12-,14+/m1/s1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)c2nc(N)s[n+]2c3ccccc3\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14N2O3S/c1-11-15(12-7-9-14(10-8-12)22(17,19)20)16(18-21-11)13-5-3-2-4-6-13/h2-10H,1H3,(H2,17,19,20)\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][=N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][=O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H12F4N4O2/c20-9-4-5-10(14(23)8-9)16-11(18(24)28)6-7-15(26-16)27(19(25)29)17-12(21)2-1-3-13(17)22/h1-8H,(H2,24,28)(H2,25,29)\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][O][C][=C][Ring1][Branch2][N][C][=Branch1][C][=O][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=Branch2][Ring1][Branch1][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=O][N][C][C@H1][Branch1][#Branch2][C][O][C][C][=C][O][N][=Ring1][Branch1][O][C][Ring1][N][=O]\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H6Cl2N2O4S2/c7-4-1-3(15(9,11)12)2-5(6(4)8)16(10,13)14/h1-2H,(H2,9,11,12)(H2,10,13,14)\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H26ClN7O2/c1-32-15-29-11-22(32)24-23-25(31-35(24)14-18-8-9-30-21-7-6-19(28)10-20(18)21)33(12-16-2-3-16)27(37)34(26(23)36)13-17-4-5-17/h6-11,15-17H,2-5,12-14H2,1H3\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H37N3O4/c1-7-8-9-16(12-24)22-19(26)18(11-14(4)5)23-20(27)17(10-13(2)3)21-15(6)25/h12-14,16-18H,7-11H2,1-6H3,(H,21,25)(H,22,26)(H,23,27)/t16-,17-,18-/m0/s1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" engineering\\n\",\n        \"output\": \" engineering is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" coffee\\n\",\n        \"output\": \" coffee is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][N][C][C][C@@][Branch2][Ring1][N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][Branch1][Branch1][C][Ring2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H17ClN2O4/c1-11-19(26-14-8-6-13(20)7-9-14)18-15(21-12(2)23)4-3-5-16(18)22(11)10-17(24)25/h3-9H,10H2,1-2H3,(H,21,23)(H,24,25)\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)OC(=O)N1CCC(CC1)Oc2ncnc3N(CCc23)c4ccc(cc4F)S(=O)(=O)C\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H15ClN2O3/c21-14-8-9-16-15(11-14)19(13-5-2-1-3-6-13)23(12-18(24)22-16)20(25)17-7-4-10-26-17/h1-11,19H,12H2,(H,22,24)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C32H40N2O5S2/c1-4-34(32(35)24-25-10-14-29(15-11-25)40(2,36)37)28-18-21-33(22-19-28)23-20-31(26-8-6-5-7-9-26)27-12-16-30(17-13-27)41(3,38)39/h5-17,28,31H,4,18-24H2,1-3H3/t31-/m0/s1\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H25ClN2O4S/c1-16-13-23(14-19-11-20(22)8-7-18(19)12-21(25)26)9-10-24(16)29(27,28)15-17-5-3-2-4-6-17/h2-8,11,16H,9-10,12-15H2,1H3,(H,25,26)/t16-/m0/s1\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][#Branch1][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H16Cl3F3N2O3S/c1-25(2)5-6-28-15-9-11(3-4-12(15)18)24-29(26,27)16-13(19)7-10(8-14(16)20)17(21,22)23/h3-4,7-9,24H,5-6H2,1-2H3\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(carbamoylamino)-5-[4-(piperidin-1-ylmethyl)phenyl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27FN4O2/c1-15-18(23(29)28-10-3-2-4-21(28)25-15)9-13-27-11-7-16(8-12-27)22-19-6-5-17(24)14-20(19)30-26-22/h5-6,14,16H,2-4,7-13H2,1H3\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)Cc1cc(Nc2ccnc3cc(Cl)ccc23)ccc1O\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(N)cccc1CN2C=CC(=CC2=O)OCCc3cccs3\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H25N5O/c1-2-19-15-24(22-9-5-6-10-23(22)26-19)31-16-17-11-13-18(14-12-17)20-7-3-4-8-21(20)25-27-29-30-28-25/h3-4,7-8,11-15H,2,5-6,9-10,16H2,1H3,(H,27,28,29,30)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H31ClN4O5/c28-20-4-5-22-26(36-17-35-22)25(20)31-27-24-21(29-16-30-27)14-19(34-11-3-10-32-8-1-2-9-32)15-23(24)37-18-6-12-33-13-7-18/h4-5,14-16,18H,1-3,6-13,17H2,(H,29,30,31)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2]\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-5-methyl-n'-(5-methyl-1h-pyrazol-3-yl)pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2SCC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)Cc1ccccc1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CS(=O)(=O)c1ccc(cc1Cl)[C@@H](C[C@H]2CCC(=O)C2)C(=O)Nc3cnccn3\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-n-[2-(1,3-benzodioxol-5-yl)ethyl]-1-(2-imidazol-1-yl-6-methylpyrimidin-4-yl)pyrrolidine-2-carboxamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccccc34)c2C(=O)N5CC[C@@H](O)C5\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOc1ccccc1c2ccc3c(c2)C(=O)C(=O)c4ccccc34\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H28ClFN6O2/c1-31-9-7-24(8-10-31,23(27)33)32(2)13-15-11-16-19(12-20(15)34-3)28-14-29-22(16)30-18-6-4-5-17(25)21(18)26/h4-6,11-12,14H,7-10,13H2,1-3H3,(H2,27,33)(H,28,29,30)\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H13FN6O3/c20-14-5-1-2-6-15(14)24-19-26-25-18(29-19)17(27)23-12-7-8-16(22-10-12)28-13-4-3-9-21-11-13/h1-11H,(H,23,27)(H,24,26)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-chloro-n-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-2-methoxybenzamide\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-ethyl-5-phenylimidazolidine-2,4-dione\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CCN(C)C)S(=O)(=O)c1ccc(cc1)c2cnc(N)c(n2)C(=O)Nc3cccnc3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][N][C][O][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H16N2O2/c22-19(21-14-15-10-12-20-13-11-15)16-6-8-18(9-7-16)23-17-4-2-1-3-5-17/h1-13H,14H2,(H,21,22)\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][N][N][C][=Branch1][C][=O][C][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(Br)c2ccccc12\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][=C][C][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][Ring1][#C]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[6-chloro-2-(3-hydroxypropylamino)quinolin-5-yl]-2-cyclohexylacetamide\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" experience\\n\",\n        \"output\": \" experience is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CCO)CCCOc1cc2ncnc(Nc3cc(CC(=O)Nc4cccc(F)c4)[nH]n3)c2cc1OC\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-[2-[[(2r)-2-hydroxy-2-(4-hydroxy-3-methanesulfonamidophenyl)ethyl]amino]-2-methylpropyl]phenyl]-n-[[3-(4-hydroxyphenyl)phenyl]methyl]acetamide\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][N][=C][N][=C][Ring2][Ring1][Branch2][C][=C][Ring2][Ring1][N][O][C][C][C][N][Branch1][Ring2][C][C][O][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-dimethylaminonaphthalene-1-sulfonamide\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-n-[2-chloro-4-(prop-2-enylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H8N2OS/c13-9(8-4-2-1-3-5-8)12-10-11-6-7-14-10/h1-7H,(H,11,12,13)\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H19N7O/c1-13-6-3-4-9-16(13)29-17(27-15-8-5-7-14(2)18(15)22(29)30)10-28-12-26-19-20(23)24-11-25-21(19)28/h3-9,11-12H,10H2,1-2H3,(H2,23,24,25)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (3r,6s,9r,12r)-6-cyclopropyl-12-[(4-fluorophenyl)methyl]-3,8,9-trimethyl-2-oxa-5,8,11,14-tetrazabicyclo[16.4.0]docosa-1(22),18,20-triene-7,10,13-trione\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H8N2O3S2/c12-7-1-3-8(4-2-7)16(13,14)11-9-10-5-6-15-9/h1-6,12H,(H,10,11)\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H23NO3/c1-13(12-22-17-6-4-3-5-7-17)19-14(2)18(21)15-8-10-16(20)11-9-15/h3-11,13-14,18-21H,12H2,1-2H3\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" lion\\n\",\n        \"output\": \" lion is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1C=C(Nc2ccccc12)c3occc3\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1nc(Br)cnc1NS(=O)(=O)c2cccc3c(cccc23)N(C)C\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H29N5O4/c1-31-19-2-3-20-21(13-19)29(24(30)16-27-20)9-8-28-6-4-17(5-7-28)25-14-18-12-22-23(15-26-18)33-11-10-32-22/h2-3,12-13,15-17,25H,4-11,14H2,1H3\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" appeal\\n\",\n        \"output\": \" appeal is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(9-ethylcarbazol-3-yl)-2-methylpropanamide\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][N][C][O][C][=C][C][=C][Branch1][=C][C][C][=C][N][=C][Branch1][C][N][N][=C][Ring1][#Branch1][N][C][=C][Ring1][#C][O][C][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-hydroxyphenyl)-1h-quinolin-4-one\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC1(CCN(CC1)c2ncnc3[nH]ccc23)C(=O)NCc4ccc(Cl)cc4\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ncnc2nc(cc(c3cccc(Br)c3)c12)c4ccc(nc4)N5CCOCC5\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H26ClN5O2/c1-15-4-9-19(23)20(12-15)26-21-10-11-24-22(27-21)25-16-5-7-18(8-6-16)30-14-17(29)13-28(2)3/h4-12,17,29H,13-14H2,1-3H3,(H2,24,25,26,27)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCN(C)C\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][Ring1][O][C][=Branch1][C][=O][N][C][C][N][C][C][C][Ring1][#Branch1][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][S][C][=Branch1][Ring2][=N][Ring1][Branch1][N][Branch1][N][C][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(2-fluorophenyl)-1-(2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl)urea\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H23F3N4O5S/c1-12(2)17(18(29)20(21,22)23)25-16(28)11-27-15(13-7-5-4-6-8-13)10-9-14(19(27)30)26-33(31,32)24-3/h4-10,12,17,24,26H,11H2,1-3H3,(H,25,28)\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-bromophenyl)sulfonyl-n-[(4-fluorophenyl)methyl]propanamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H26ClN5O2/c1-15-4-9-19(23)20(10-15)27-22-11-21(24-14-25-22)26-16-5-7-18(8-6-16)30-13-17(29)12-28(2)3/h4-11,14,17,29H,12-13H2,1-3H3,(H2,24,25,26,27)\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H26ClN7O3/c1-15-2-4-18(13-26-15)35-20-5-3-16(12-19(20)25)29-22-21-23(28-14-27-22)30-31-24(21)34-11-10-32-8-6-17(33)7-9-32/h2-5,12-14,17,33H,6-11H2,1H3,(H2,27,28,29,30,31)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H10O3/c1-2-13-9-5-3-8-4-6-11(12)14-10(8)7-9/h3-7H,2H2,1H3\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,5-bis(4-chlorophenyl)-3-propan-2-yliminophenazin-2-amine\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(2-fluorophenyl)methylcarbamoylamino]-3-phenyl-n,n-di(propan-2-yl)-2-pyridin-3-ylbutanamide\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[(4-methoxyphenyl)amino]benzoic acid\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-7-methoxy-1,8-naphthyridin-2-one\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H10O5/c16-9-2-3-10-14(6-9)20-7-11(15(10)19)8-1-4-12(17)13(18)5-8/h1-7,16-18H\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H17BrN2O2/c15-11-1-3-13(4-2-11)19-14(18)17-10-9-16-7-5-12(17)6-8-16/h1-4,12H,5-10H2\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H20O5/c1-3-4-16-17(10-9-15(12(2)20)18(16)21)24-11-13-5-7-14(8-6-13)19(22)23/h5-10,21H,3-4,11H2,1-2H3,(H,22,23)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2CCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][C][=C][C][=C][Branch2][Ring2][#Branch1][N][C][=Branch1][C][=O][C][=C][C][Branch1][#Branch2][N][C][=N][C][=C][C][=N][Ring1][=Branch1][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][P][\\\\C][=Branch1][Ring1][=N][\\\\O][\\\\N][C][=C][Ring2][Ring1][=C]\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H4Cl2O/c7-4-1-5(8)3-6(9)2-4/h1-3,9H\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(Nc2nnc(Cc3ccncc3)c4ccccc24)cc1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-(4-methoxyphenyl)-4-(trifluoromethyl)phenoxy]acetic acid\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H](NC(=O)Cc1cc(F)cc(F)c1)C(=O)NC2C(=O)N(C)c3ccccc3c4ccccc24\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl 8-[(9,10-dioxophenanthren-2-yl)amino]-8-oxooctanoate\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][O][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][B][N][Branch1][S][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1nc(Cl)cnc1NS(=O)(=O)c2cccc3c(cccc23)N(C)C\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][Branch1][C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H12F4N2OS/c1-7(8-5-3-4-6-9(8)14)18-11-19-10(20)12(2,21-11)13(15,16)17/h3-7H,1-2H3,(H,18,19,20)/t7-,12?/m0/s1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring1][=N]\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H9Br2N5/c14-8-2-1-3-9(15)10(8)7-4-6-5-18-13(17)20-12(6)19-11(7)16/h1-5H,(H4,16,17,18,19,20)\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(C)c2c(N)c(sc2n1)C(=O)NC3CC3\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][S][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][=Branch1][C][=O][\\\\C][=C][\\\\C][=C][N][=C][N][C][=Branch1][C][=O][C][C][C][Ring1][#Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[[3-(trifluoromethyl)phenyl]amino]benzoic acid\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H19NO3S/c1-27-20-11-12-21(26-15-16-5-3-2-4-6-16)17(13-20)7-9-19-10-8-18(14-23-19)22(24)25/h2-14H,15H2,1H3,(H,24,25)/b9-7+\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,8-naphthyridine-3-carboxylic acid\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(2-methoxyphenyl)methyl]-n-[4-(phenoxy)pyridin-3-yl]acetamide\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1c(N2CCO[C@@H](CN(C)C)C2)c(F)cc3C(=O)C(=CN(C4CC4)c13)C(=O)O\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=Branch1][Ring2][=C][Ring1][#Branch1][N][C][=N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][P][C][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)Nc1cc(sc1C(=O)N[C@H]2CCCNC2)c3cccc(F)c3F\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)c2cc(Nc3cc(C)[nH]n3)nc(Sc4ccc(NC(=O)C5CC5)cc4)n2\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H26ClN/c1-13(2)12-16(19(3)4)17(10-5-11-17)14-6-8-15(18)9-7-14/h6-9,13,16H,5,10-12H2,1-4H3\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2,3-dihydrothieno[3,4-b][1,4]dioxin-7-yl-(4-methylpiperidin-1-yl)methanone\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (e)-n-(2-aminophenyl)-3-[4-[(3,4-dimethoxyphenyl)sulfonylamino]phenyl]prop-2-enamide\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][O][C][=N][C][=C][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=N][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" memory\\n\",\n        \"output\": \" memory is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][=Branch1][F]\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H12N4O2/c1-18-9-4-2-8(3-5-9)15-11(17)10-6-7-14-12(13)16-10/h2-7H,1H3,(H,15,17)(H2,13,14,16)\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O]\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18N6O2S/c1-25(17-8-4-7-16-15(17)12-21-24-16)18-9-10-20-19(23-18)22-13-5-3-6-14(11-13)28(2,26)27/h3-12H,1-2H3,(H,21,24)(H,20,22,23)\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1SC(=O)c2cc(ccc12)S(=O)(=O)N\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)C(=O)CS(=O)(=O)c2ccccc2\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-ethoxy-1,3-benzothiazol-2-amine\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CS(=O)(=O)n1c2ccccc2c3cc(NC(=O)N4CCOCC4)ccc13\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H6N2OS2/c13-9-8-6(7-2-1-3-14-7)4-15-10(8)12-5-11-9/h1-5H,(H,11,12,13)\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14+,19-,20+/m0/s1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" heron\\n\",\n        \"output\": \" heron is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H19N3O2/c19-18(23)21-17(22)16(13-5-2-1-3-6-13)20-15-10-9-12-7-4-8-14(12)11-15/h1-3,5-6,9-11,16,20H,4,7-8H2,(H3,19,21,22,23)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H16ClN3O3S/c19-15-9-11-8-12(21-17(11)26-15)16(24)20-13-7-10-3-1-2-4-14(10)22(5-6-23)18(13)25/h1-4,8-9,13,21,23H,5-7H2,(H,20,24)\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [4-(phenylmethyl)piperidin-1-yl]-(1-propylsulfonylpiperidin-3-yl)methanone\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(3-ethyl-1-methylazepan-3-yl)phenol\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][=N][\\\\C][=C][\\\\S][C][=Branch1][C][=O][N][C][/-Ring1][=Branch1][=O][=C][C][Branch1][Ring1][O][C][=C][Ring1][S][O]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][Branch2][Ring1][=C][C][C][N][Branch2][Ring1][Ring1][C][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2cccnc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (3r,5r)-7-[(1s,2s,6s,8s,8ar)-6-hydroxy-2-methyl-8-[(2s)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid\\n\",\n        \"output\": \" -0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)NC(=O)c1cnc(N2CCC(CC2)N3C(=O)OCc4ccccc34)c(Cl)c1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[3-(1-adamantylmethylcarbamoyl)-4-chlorophenyl]benzoic acid\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][O][C][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][C][N][=N][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][S][=C][C][=C][Ring1][=Branch1][O][C][C][N][C][C][C][C][Ring1][Branch1][N][C][=N][C][C][=C][Branch1][=Branch2][S][C][=Ring1][Branch1][C][Ring1][=Branch2][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-amino-n-(1,3-thiazol-2-yl)benzenesulfonamide\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H12FN3O3/c1-19-14-7-6-10(20(22)23)8-12(14)16(18-9-15(19)21)11-4-2-3-5-13(11)17/h2-8H,9H2,1H3\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][#C][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1][N][C][C][C][C@@H1][Ring1][Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][C][=C][Branch1][=Branch1][S][C][=Ring1][Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][C][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H11N3O2S/c12-9-4-6-10(7-5-9)17(15,16)14-11-3-1-2-8-13-11/h1-8H,12H2,(H,13,14)\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ray\\n\",\n        \"output\": \" ray is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-5-chloro-n-[(3s,4r)-1-[3-(4-fluorophenoxy)propyl]-3-methoxypiperidin-4-yl]-2-methoxybenzamide\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 8-chloro-6-(2-chlorophenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H16N2O3S2/c1-2-7-20-14-16-10-4-3-9(8-11(10)21-14)15-12(17)5-6-13(18)19/h3-4,8H,2,5-7H2,1H3,(H,15,17)(H,18,19)\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring2][C][O][C][C][C][O][C][Branch1][=Branch2][C][N][C][=C][N][=C][Ring1][Branch1][Branch1][Ring2][O][Ring1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][C][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H24N4S/c20-15(18-13-4-2-1-3-5-13)19-8-6-12(7-9-19)14-10-16-11-17-14/h10-13H,1-9H2,(H,16,17)(H,18,20)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H26F3N3O6S/c1-16(2)23(24(34)26(27,28)29)30-22(33)15-32-21(17-7-5-4-6-8-17)14-13-20(25(32)35)31-39(36,37)19-11-9-18(38-3)10-12-19/h4-14,16,23,31H,15H2,1-3H3,(H,30,33)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-chloro-2-(4-ethylsulfonylphenyl)phenoxy]acetic acid\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H21NO2S/c1-15(2,16-8-10-18-11-9-16)14(17)12-4-6-13(19-3)7-5-12/h4-7H,8-11H2,1-3H3\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(cc1)[C@@H]2CCNC[C@H]2COc3ccc4OCOc4c3\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch1][#Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" coach\\n\",\n        \"output\": \" coach is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H25N7O3S/c1-15-12-17(33(31,32)29-10-8-28(2)9-11-29)5-6-18(15)19-14-25-21(23)20(27-19)22(30)26-16-4-3-7-24-13-16/h3-7,12-14H,8-11H2,1-2H3,(H2,23,25)(H,26,30)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" FC(F)(F)CCS(=O)(=O)Oc1ccc(NC(=O)c2ccc(Cn3ccnn3)c4ccccc24)c(n1)C(=O)NCC5CCOCC5\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][Branch1][=C][C][=N][C][=N][C][Branch1][C][N][=C][Ring1][#Branch2][Ring1][#Branch1][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20ClFN4O2/c1-25(2)6-7-27-18-9-13-16(10-17(18)26-3)22-11-23-19(13)24-12-4-5-15(21)14(20)8-12/h4-5,8-11H,6-7H2,1-3H3,(H,22,23,24)\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc2NC(=O)CN(C(c3ccccc3)c2c1)C(=O)c4occc4\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-chlorophenyl)quinazolin-4-amine\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H22F3N7O3S/c1-31-7-9-32(10-8-31)36(34,35)15-4-5-16(17(11-15)22(23,24)25)18-13-28-20(26)19(30-18)21(33)29-14-3-2-6-27-12-14/h2-6,11-13H,7-10H2,1H3,(H2,26,28)(H,29,33)\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)NCC(O)COc1ccc(CCOCC2CC2)cc1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H17ClN2O2/c23-17-11-12-19-18(13-17)21(15-7-3-1-4-8-15)25(14-20(26)24-19)22(27)16-9-5-2-6-10-16/h1-13,21H,14H2,(H,24,26)\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nnc(s1)c2ccccc2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc2Oc3ccccc3N=C(N4CCNCC4)c2c1\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C(Cc1nc2ccccc2[nH]1)Cc3nc4ccccc4[nH]3\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H31N3O3/c1-16(2)20-11-21(23(29)12-22(20)28)24(30)27-14-18-5-4-17(10-19(18)15-27)13-26-8-6-25(3)7-9-26/h4-5,10-12,16,28-29H,6-9,13-15H2,1-3H3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10N2O/c15-12(10-6-2-1-3-7-10)14-11-8-4-5-9-13-11/h1-9H,(H,13,14,15)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H25N3O2/c1-22-21(25)17-6-8-20(23-14-17)26-19-7-5-15-9-11-24(18-3-2-4-18)12-10-16(15)13-19/h5-8,13-14,18H,2-4,9-12H2,1H3,(H,22,25)\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1OC)c2csc(NC(=O)c3c(C)onc3C)n2\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H24F3N3O3S/c1-14(2)13-30-22-19(20(31)28(3)23(30)33)18(21(32)29-10-6-7-11-29)17(34-22)12-15-8-4-5-9-16(15)24(25,26)27/h4-9,14H,10-13H2,1-3H3\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cccc(CN2CCN(CC2)C(c3ccccc3)c4ccc(Cl)cc4)c1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-dimethylamino-1,5-dimethyl-2-phenylpyrazol-3-one\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NS(=O)(=O)c1ccc(NCc2ccccc2)cc1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H19N3O3/c1-21-14-8-11(9-15(22-2)16(14)23-3)10-18-17-19-12-6-4-5-7-13(12)20-17/h4-9H,10H2,1-3H3,(H2,18,19,20)\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring2][Ring1][Ring1][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C][C][N][C][Branch2][Ring1][C][S][C][=N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][S][Ring1][#Branch2][=N][C][=C][Branch1][C][N][N][=C][N][=C][Ring2][Ring1][Branch1][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H16O3/c1-2-25-20-10-6-5-7-15(20)14-11-12-17-16-8-3-4-9-18(16)21(23)22(24)19(17)13-14/h3-13H,2H2,1H3\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(CN1CCCCC1)C(=O)c2ccc(C)cc2\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-chloro-1-methyl-5-phenyl-3h-1,4-benzodiazepin-2-one\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-piperidin-4-yloxybenzamide\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(cyclohexanecarbonyl)-3,6,7,11b-tetrahydro-1h-pyrazino[6,1-a]isoquinolin-4-one\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=N][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][Ring1][S]\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCCOCCOCCc1cccc2ccccc12)c3ccc(O)c4NC(=O)Sc34\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][C][=N][NH1][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H9FN2/c14-11-6-4-10(5-7-11)12-9-16-8-2-1-3-13(16)15-12/h1-9H\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C@H1][C][C][C@H1][C@@H1][C][C][C][=C][C][=Branch1][C][=O][C][C][C@][Ring1][#Branch1][Branch1][C][C][C@H1][Ring1][N][C][C][C@][Ring2][Ring1][Ring1][Ring1][S][C]\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1OC)C(=O)Nc2cccc(NC(=O)c3ccc(OC)c(OC)c3)n2\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(NCc3ccccc3)c2cc1OC\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCS(=O)(=O)c1ccc(cc1)c2cc(Cl)ccc2OCC(=O)O\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H23N3O2/c1-14(2)23-18-6-4-3-5-16(18)17-13-15(7-8-19(17)23)21-20(24)22-9-11-25-12-10-22/h3-8,13-14H,9-12H2,1-2H3,(H,21,24)\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][Branch2][Ring1][Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=N][N][=N][N][Ring1][Branch1][C][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@@H1][N][C][Branch1][C][C][Branch1][C][C][C][O][C@@][Ring1][Branch2][Branch1][C][O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H14N2O2S/c1-14(2)11-7-3-6-10-9(11)5-4-8-12(10)17(13,15)16/h3-8H,1-2H3,(H2,13,15,16)\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(carbamoylamino)-5-[4-(2-dimethylaminoethoxy)phenyl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" [O-][N+](=O)c1cccc2ccc(nc12)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCc1cc(ccn1)C(=S)N\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H24N4O4/c1-26-8-6-14(7-9-26)30-19-11-15(27-2)10-17-20(19)22(24-12-23-17)25-16-4-3-5-18-21(16)29-13-28-18/h3-5,10-12,14H,6-9,13H2,1-2H3,(H,23,24,25)\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-[(1-oxidopyridin-1-ium-4-yl)methylcarbamoylamino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(CCc1ccccc1)NCC(O)c2ccc(O)c(c2)C(=O)N\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H19ClN4O3/c18-14-7-6-12(22-17(25)21-15(23)10-20-22)8-13(14)16(24)19-9-11-4-2-1-3-5-11/h6-8,10-11H,1-5,9H2,(H,19,24)(H,21,23,25)\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (3r,4s,5s,6r,7r,9r,10e,11s,12r,13s,14r)-6-[(2s,3r,4s,6r)-4-dimethylamino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2r,4r,5s,6s)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-(2-methoxyethoxymethoxyimino)-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecan-2-one\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4,6-dimethylpyridin-2-amine\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-chloro-2-(4-ethylsulfonyl-2-methylphenyl)phenoxy]acetic acid\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][Branch1][Ring1][C][O][N][C][C][N][C][Branch1][Ring1][C][C][C][O]\\n\",\n        \"output\": \" -1.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC[C@@H](NC1=C(Nc2cccc(C(=O)N(C)C)c2O)C(=O)C1=O)c3ccccc3\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H24N4O/c1-24-21-13-14-27(16-21)22-12-11-20(15-25-22)26-23(28)19-9-7-18(8-10-19)17-5-3-2-4-6-17/h2-12,15,21,24H,13-14,16H2,1H3,(H,26,28)\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-fluorophenyl)-2-(phenoxy)pyridine-3-carboxamide\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NNC1=Nc2ccccc2NC1=O\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-n-(2,6-dimethoxypyrimidin-4-yl)benzenesulfonamide\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H22N2O5S/c1-12-9-14-7-5-6-8-16(14)21(12)27(23,24)19-10-15(20-13(2)22)17(25-3)11-18(19)26-4/h5-8,10-12H,9H2,1-4H3,(H,20,22)\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][Branch2][Ring1][=Branch2][C@@H1][C][C][N][Branch1][S][C][C][C][=C][C][=C][O][C][C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][Ring1][S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NCc1ccc(NC(=O)c2cc(Nc3ncccn3)c4cc(ccc4c2)\\\\C(=N\\\\O)\\\\N)cc1\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(O)c2C(=O)O[C@@H](C)C\\\\C=C/C(=O)[C@@H](O)[C@@H](O)C\\\\C=C\\\\c2c1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H28Cl2N2O3/c25-21-7-6-20(16-22(21)26)31-19-10-14-27(15-11-19)18-8-12-28(13-9-18)23(24(29)30)17-4-2-1-3-5-17/h1-7,16,18-19,23H,8-15H2,(H,29,30)\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-amino-n-cyclopropyl-4,6-dimethylthieno[5,4-b]pyridine-2-carboxamide\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H27NO2/c1-3-19(4-2)14-15-21-17(20)18(12-8-9-13-18)16-10-6-5-7-11-16/h5-7,10-11H,3-4,8-9,12-15H2,1-2H3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NS(=O)(=O)c1cc(Cl)c(Cl)c(c1)S(=O)(=O)N\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2nccc([C@@H](O)[C@@H]3C[C@H]4CCN3C[C@@H]4C=C)c2c1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-chloro-2-(1-thiophen-3-ylethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)NCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nccc(\\\\C=C\\\\c2ccc(Cl)cc2)n1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][S][C][=Branch1][=Branch1][=C][C][=Ring1][Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CSc1ccc(cc1)N2C(=NC(=NC2(C)C)N)N\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H28N2O4/c1-5-6-18(23)20-14-7-8-17(16(9-14)13(4)21)24-11-15(22)10-19-12(2)3/h7-9,12,15,19,22H,5-6,10-11H2,1-4H3,(H,20,23)\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-pyrrolidin-1-yl-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[5-(4-fluorophenyl)-3-piperidin-4-ylimidazol-4-yl]pyridine\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[(1r,2r)-2-[(5-chloro1h-indole-2-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]acetic acid\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][N][Branch2][Ring1][#Branch2][C][C][C][=C][C][=C][Branch1][=C][O][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H35N7O3/c1-20-5-6-23(31-27(36)22-7-9-29-26(16-22)35-12-14-37-15-13-35)17-24(20)32-25-8-10-30-28(33-25)38-19-21-4-3-11-34(2)18-21/h5-10,16-17,21H,3-4,11-15,18-19H2,1-2H3,(H,31,36)(H,30,32,33)\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nc(cs1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-[(1-ethoxy-1-oxo-4-phenylbutan-2-yl)amino]-2-oxo-4,5-dihydro-3h-1-benzazepin-1-yl]acetic acid\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-chloro-2-(furan-3-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)c1cccc2c(cccc12)S(=O)(=O)N(C)CC(=O)O\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@@][Branch1][C][O][Branch2][Ring1][=Branch2][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16ClNO2S/c1-20-16(19)15(12-4-2-3-5-13(12)17)18-8-6-14-11(10-18)7-9-21-14/h2-5,7,9,15H,6,8,10H2,1H3/t15-/m0/s1\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(CN2C(=O)CCSc3ccc(Cl)cc23)cc1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][Ring1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][N][=C][C][=N][Ring1][=Branch1][C][Branch1][C][F][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-amino-6-[4-(4-methylpiperazin-1-yl)sulfonyl-2-(trifluoromethyl)phenyl]-n-pyridin-3-ylpyrazine-2-carboxamide\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][Branch1][C][F][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring2][=Branch1][N][C][=Branch1][C][=O][N][C][C][N][Branch2][Ring1][Branch1][C][C@@H1][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=N][C][C][Ring2][Ring1][Ring2][C][=C][Ring2][Ring1][=N][Cl]\\n\",\n        \"output\": \" 4.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][Branch1][N][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][=C][Ring1][#C]\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" stitch\\n\",\n        \"output\": \" stitch is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCCOc1nn(Cc2ccccc2)c3ccccc13\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][NH1][C][Branch2][Ring1][C][\\\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][\\\\-Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)C1CCn2c1ccc2C(=O)c3ccccc3\\n\",\n        \"output\": \" -0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H9N3/c9-5-8-10-6-3-1-2-4-7(6)11-8/h1-4H,5,9H2,(H,10,11)\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" wave\\n\",\n        \"output\": \" wave is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H6N2S/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H2,8,9)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)c1c(O)cccc1OC\\\\C=C\\\\c2ccc(F)c(c2)c3onc(c3)C(=O)O\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(CC2=NNC(=O)c3ccccc23)cc1C(=O)N4CCCNCC4\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H16F2N4O4S/c18-15-7-12(1-2-14(15)11-3-5-28(25,26)6-4-11)22-9-13(27-17(22)24)10-23-16(19)8-20-21-23/h1-3,7-8,13H,4-6,9-10H2/t13-/m1/s1\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1N2CCOC2=Nc3ccccc13\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1nnsc1C(=O)Nc2ccccc2\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=Branch2][Ring1][C][=C][C][=C][Ring1][=Branch1][N][C][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-chloro-3-[(1-hydroxycycloheptyl)methylcarbamoyl]phenyl]benzoic acid\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-hydroxy-2-(4-hydroxyphenyl)chromen-4-one\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n'-di(phenyl)-1h-pyrazole-3,5-diamine\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccnc(NCc2c(O)ccc3ccccc23)c1\\n\",\n        \"output\": \" 4.24\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H13Cl2NO2S/c1-10-17(23-13-5-2-11(18)3-6-13)14-7-4-12(19)8-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H13N3O2/c16-12-9-11(14-5-7-17-8-6-14)13-10-3-1-2-4-15(10)12/h1-4,9H,5-8H2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H12N2O/c1-9-8-11(14)13(12(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[3-(4-methylsulfonylphenyl)-3-phenylpropyl]piperidin-4-yl]acetamide\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H26F3N5O5/c1-16(2)22(23(36)26(27,28)29)32-21(35)15-34-20(18-6-4-3-5-7-18)9-8-19(24(34)37)31-25(38)30-14-17-10-12-33(39)13-11-17/h3-13,16,22H,14-15H2,1-2H3,(H,32,35)(H2,30,31,38)\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H14N4O/c1-16(2)12-10(17-3)8-14-11(15-12)9-6-4-5-7-13-9/h4-8H,1-3H3\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CS(=O)(=O)c1ccc(c[n+]1[O-])C(=O)Nc2ccc(F)cc2\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H31F3N4O5/c1-16(2)21(22(35)26(27,28)29)32-20(34)14-33-23(18-11-7-4-8-12-18)30-13-19(24(33)36)31-25(37)38-15-17-9-5-3-6-10-17/h3,5-6,9-10,13,16,18,21H,4,7-8,11-12,14-15H2,1-2H3,(H,31,37)(H,32,34)\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(C(=O)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCC1(C)CC(=O)NC1=O\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)C[C@H](O)Cc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfanyl-2-methyl-4-phenylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21ClN4/c1-22-18-5-3-2-4-17(18)21-19(22)14-23-10-12-24(13-11-23)16-8-6-15(20)7-9-16/h2-9H,10-14H2,1H3\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][C][Branch1][Branch1][C][C][Ring1][#Branch1][N][N][=C][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1csc(NC(=O)c2cc(Sc3nncn3C)ccc2N)n1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCO\\\\N=C(\\\\C1CCN(CC1)C2(C)CCN(CC2)C(=O)c3c(Cl)cncc3Cl)/c4ccc(Br)cc4\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][C@H1][Branch1][C][C][O][C][=C][C][Branch1][S][O][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][=C][C][=Branch1][Ring2][=C][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H14N2S/c1-2-6-11-10(5-1)14-12(15-11)9-4-3-7-13-8-9/h1-2,5-6,9,13H,3-4,7-8H2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][N][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring1][=C]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)NCCCOc1ccc(NC(=O)C)cc1CC=C\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][C][=C][Branch1][#Branch2][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H31N3O/c1-29(27(31)24-12-17-28-18-13-24)25-14-19-30(20-15-25)21-16-26(22-8-4-2-5-9-22)23-10-6-3-7-11-23/h2-13,17-18,25-26H,14-16,19-21H2,1H3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" index\\n\",\n        \"output\": \" index is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][O][C@H1][C][C][C@H1][C@@H1][C][C][C][=C][C][=Branch1][C][=O][C][C][C@][Ring1][#Branch1][Branch1][C][C][C@H1][Ring1][N][C][C][C@][Ring2][Ring1][Ring1][Ring1][S][C]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" paper\\n\",\n        \"output\": \" paper is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCN(CCO)CCCOc1ccc2c(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)ncnc2c1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][=Branch2][C][=C][C][C][C][C][Ring1][=Branch1][C][Ring1][#C][=O]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCC1(C(=O)NC(=O)NC1=O)c2ccccc2\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc2ncccc2c1C(=O)NCC3CCCCC3\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=C2C(=CC(=O)N1Cc3ccccn3)NN(C2=O)c4ccccc4Cl\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(Cc2c(N)n[nH]c2N)cc1\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H11NO3S2/c1-15-8-4-3-7(5-9(8)16-2)6-10-11(14)13-12(17)18-10/h3-6H,1-2H3,(H,13,14,17)/b10-6-\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(N[C@@H]1CN2CCC1CC2)c3ccc(s3)c4ccccc4\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(3,4-dichlorophenyl)-n-methyl-n-[(1s)-1-phenyl-2-pyrrolidin-1-ylethyl]acetamide\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(phenylmethylsulfonyl)piperidine-1-carboxamide\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(C(=O)OC1CN2CCC1CC2)(c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-2-(3-chloro-4-methylsulfonylphenyl)-3-[(1r)-3-oxocyclopentyl]-n-pyrazin-2-ylpropanamide\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)c1sc2nccc(Nc3ccccc3)c2c1N\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H28N2O5S/c25-18-8-7-17(21-20(18)24-22(27)30-21)19(26)15-23-10-4-11-28-13-14-29-12-9-16-5-2-1-3-6-16/h1-3,5-8,19,23,25-26H,4,9-15H2,(H,24,27)/t19-/m0/s1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C(Oc1cccc2ccccc12)C3=NCCN3\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccccc1Cn2c(C)nc3ccccc23\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1CO)c2ccc3c(nc(nc3n2)N4C[C@@H](C)O[C@@H](C)C4)N5CCOCC5\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-fluoro-4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-methylbenzamide\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][N][C][=N][C][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12N2O/c18-15-13-9-5-4-8-12(13)14(16-17-15)10-11-6-2-1-3-7-11/h1-9H,10H2,(H,17,18)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)-6-naphthalen-1-yloxythieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[[4-[(4-phenylpiperazin-1-yl)methyl]phenyl]methyl]acetamide\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch1][#Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][O][C][C][O][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][=Branch1][C][=O][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][N][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" violin\\n\",\n        \"output\": \" violin is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H8Cl2N2S/c12-8-2-1-7(5-9(8)13)10-6-16-11-14-3-4-15(10)11/h1-2,5-6H,3-4H2\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H28FN5O3/c1-29-6-8-31(9-7-29)22-15-17(26)14-20-23(32)16-21(28-24(20)22)25(33)27-18-2-4-19(5-3-18)30-10-12-34-13-11-30/h2-5,14-16H,6-13H2,1H3,(H,27,33)(H,28,32)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H24N2O3S2/c19-16(17-14-7-2-1-3-8-14)13-6-4-10-18(12-13)23(20,21)15-9-5-11-22-15/h5,9,11,13-14H,1-4,6-8,10,12H2,(H,17,19)\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NS(=O)(=O)c1cc2c(NCNS2(=O)=O)cc1Cl\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)Cc1csc(n1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)CC(C)(CCc2cccc(c2)c3ccccc3)N=C1N\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=C(CCC(=O)O)C(=O)Oc2cc(O)ccc12\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(phenylmethylamino)benzenesulfonamide\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H18N2O3S/c1-3-4-9-13-12(15)14-18(16,17)11-7-5-10(2)6-8-11/h5-8H,3-4,9H2,1-2H3,(H2,13,14,15)\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-ethylpiperazin-1-yl)-n-[4-(2-morpholin-4-yl-4-oxochromen-8-yl)dibenzothiophen-1-yl]acetamide\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-diethylaminoethyl)-2-methoxy-5-methylsulfonylbenzamide\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-n-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]acetamide\\n\",\n        \"output\": \" -0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][N][C][S][C][Branch1][S][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][=C][Branch1][C][N][C][Ring2][Ring1][Ring2][=Ring1][#C]\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cccc(c1)C(=O)N2CCC(CC2)N3C(=O)Nc4ccccc34\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(CN2C(=O)CCC2(C)C(=O)NC3CCCCC3)c(OC)c1\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-2-[[2-amino-5-[(3-chlorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-[4-(diethylsulfamoyl)phenyl]-4-(trifluoromethyl)phenoxy]acetic acid\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][=C][N][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H8ClN5S/c10-5-1-2-6-8(15-16-14-6)7(5)13-9-11-3-4-12-9/h1-2H,3-4H2,(H2,11,12,13)\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC12CCC(CC1)(CC2)c3ccccc3\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(phenylmethoxy)benzamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(NS(=O)(=O)c2ccc(Cl)s2)c(c1)C(=O)Nc3ccc(cc3)S(=O)(=O)N4CCOCC4\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc2C(=O)C(=COc2c1)c3ccc(O)c(O)c3\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H29F2N3O4S/c1-17-2-5-21(6-3-17)34(31,32)27-24(30)29-12-8-18(9-13-29)28-14-10-19(11-15-28)33-20-4-7-22(25)23(26)16-20/h2-7,16,18-19H,8-15H2,1H3,(H,27,30)\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@H]1CN(Cc2ccc(F)cc2)CCN1C(=O)COc3ccc(Cl)cc3NC(=O)N\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H13ClN2/c1-10-6-7-15-13(8-10)16-9-11-2-4-12(14)5-3-11/h2-8H,9H2,1H3,(H,15,16)\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(Cl)cc1NC(=O)CCS(=O)(=O)c2ccc(Br)cc2\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[(2r)-2-amino-2-phenylethyl]-1-[(2,6-difluorophenyl)methyl]-5-(2-fluorophenyl)-6-methylpyrimidine-2,4-dione\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[3-[[7-methoxy-6-(2-pyrrolidin-1-ylethoxy)quinazolin-4-yl]amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-ethyl-1-(2-methylpropyl)imidazo[4,5-c]quinolin-4-amine\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-methoxyphenyl)-1h-quinolin-4-one\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-amino-3,6-dimethyl-6-[2-(3-phenylphenyl)ethyl]-5h-pyrimidin-4-one\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NCCCCN(Cc1nc2ccccc2[nH]1)C3CCCc4cccnc34\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H21NO4/c25-20-12-11-18-14-21(28-23(26)16-7-3-1-4-8-16)22(15-19(18)13-20)29-24(27)17-9-5-2-6-10-17/h1-10,14-15,20H,11-13,25H2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n-dimethyl-3-phenothiazin-10-ylpropan-1-amine\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-chlorophenyl)-4-(2-methylimidazo[3,2-a]pyridin-3-yl)pyrimidin-2-amine\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1cccnc1Nc2cccc(c2)C(F)(F)F\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13?,14?,19?,20-/m0/s1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2,5-dimethyl-3-(4-methylsulfonylphenyl)sulfanylindol-1-yl]acetic acid\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][N][=C][N][=C][Ring1][Branch1][C][O][C][=N][N][C][=Branch2][Ring1][C][=N][N][=C][Ring1][Branch1][C][=C][Ring1][=Branch2][C][Branch1][C][C][Branch1][C][C][C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][Branch1][C][C][=C][C][Branch2][Ring1][Branch2][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][Ring1][C]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H25ClN4O4/c1-28-7-5-14(6-8-28)11-30-20-10-17-15(9-19(20)29-2)23(26-12-25-17)27-21-16(24)3-4-18-22(21)32-13-31-18/h3-4,9-10,12,14H,5-8,11,13H2,1-2H3,(H,25,26,27)\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-4-fluoro-5-[[6-methoxy-7-(2-methoxyethoxy)quinolin-4-yl]amino]phenol\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CS(=O)(=O)c1ccc(cc1)[C@@H](O)[C@@H](CF)NC(=O)C(Cl)Cl\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H]1CN(Cc2cc(Cl)ccc2CC(=O)O)CCN1S(=O)(=O)Cc3ccccc3\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-bromo-1-phenyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-amine\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=CC(=O)Oc2c(C)c3oc(C)cc3cc12\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][C][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H23N5O2/c23-20-19(15-8-10-17(11-9-15)25-21(28)16-6-7-16)18(26-22(24)27-20)13-29-12-14-4-2-1-3-5-14/h1-5,8-11,16H,6-7,12-13H2,(H,25,28)(H4,23,24,26,27)\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[2-hydroxy-3-[(3-methoxyphenyl)methoxy]propyl]piperidine-4-carboxamide\\n\",\n        \"output\": \" -0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" cloudy\\n\",\n        \"output\": \" cloudy is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch2][Ring1][=C][C][Branch2][Ring1][C][C][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-phenylimidazo[1,2-a]pyridine\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-chloro-2-methyl-3-(2-methylphenyl)-4-oxo-1,2-dihydroquinazoline-6-sulfonamide\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H11Cl2N/c12-9-2-1-7(3-10(9)13)11-4-8(11)5-14-6-11/h1-3,8,14H,4-6H2/t8-,11+/m1/s1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)OCCn1c(Sc2nc3cccc(Cl)c3s2)nc4c(N)ncnc14\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][O][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Branch1][Ring2][N][=Ring1][O][C][C][=C][C][=C][C][=Ring1][=Branch1]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][Branch1][S][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-oxo-6-phenyl-3-(trifluoromethylsulfonylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C@@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][=N][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][O][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][C][N][C][=C][C][=C][Ring1][#Branch1][C][N][C][=C][C][=Branch1][=Branch1][=C][C][Ring1][=Branch1][=O][O][C][C][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@H1][Branch1][C][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Ring2][C@H1][Branch1][=Branch2][C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1C=C(C(=O)O)C(=O)c2cc(F)c(cc12)N3CCNCC3\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=N)SCc1ccc(Cl)c(Cl)c1\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" FC(F)(F)COc1ccc(OCC(F)(F)F)c(c1)C(=O)NCC2CCCCN2\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][N][Branch2][Branch1][Ring1][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch2][Ring1][Ring2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][=C][Ring2][Ring1][Ring2][C][C][Ring2][Ring2][Ring2]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(1-adamantyl)-n-quinolin-5-ylacetamide\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][S][C][=N][C][Branch1][#C][N][C@@H1][C][C@H1][Ring1][Ring1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][N][=N][N][Branch1][S][C@@H1][C][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O][C][Ring1][=C][=N][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4cccnn34)cc1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)C2CC(=O)c3ccc(O)cc3O2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][=Ring1][=Branch2]\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][C][=Branch1][C][=O][N][C][C@H1][Branch1][Ring2][C][C][F][C][=Ring1][#Branch2][NH1][Ring1][=N]\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(4-bromophenyl)methyl]-3-methylbenzimidazol-2-one\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch2][Ring1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][Branch1][C][N][C][C][C][S][C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1cccnc1Oc2ccccc2\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][N][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1,2,3,4-tetrahydroacridin-9-amine\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][Branch2][Ring1][#Branch2][C][C][O][C][=C][C][=C][Branch1][=N][C][C][S][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=O][C][=C][Ring1][=C][N][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][N][C][Branch1][=C][C][C][C][=C][C][Ring1][Branch1][C][Ring1][=Branch2][=C][Ring1][=N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H16N4O4/c1-14-10-20(28-17-6-7-18-19(11-17)27-13-26-18)24-21(23-14)29-16-4-2-15(3-5-16)25-9-8-22-12-25/h2-12H,13H2,1H3\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H24Cl2N2O/c1-24(21(26)14-16-9-10-18(22)19(23)13-16)20(15-25-11-5-6-12-25)17-7-3-2-4-8-17/h2-4,7-10,13,20H,5-6,11-12,14-15H2,1H3\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][C][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C@@H1][Branch1][C][O][C@@H1][Branch1][C][O][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N]\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1cnc(N[C@H]2CCCNC2)c3cc(sc13)c4ccc(F)c(F)c4\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@][C][C][C@H1][C@@H1][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C@@H1][Ring1][#C][C][C][C@@H1][Ring2][Ring1][C][O]\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H7NO2/c15-12-9-5-2-1-4-8(9)11-10(13(12)16)6-3-7-14-11/h1-7H\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)c1ccc(OCC(=O)COc2ccc(SCCCCCc3ccccc3)cc2)cc1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-[4-[(4-ethylpiperazin-1-yl)methyl]phenyl]-n-[(1r)-1-phenylethyl]-7h-pyrrolo[3,2-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H28N6O/c1-2-3-10-22-26-25(15-6-7-16-25)24(32)31(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23-27-29-30-28-23/h4-5,8-9,11-14H,2-3,6-7,10,15-17H2,1H3,(H,27,28,29,30)\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(cc1C(=O)NCCc2ccccc2)N3N=CC(=O)NC3=O\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-[[3,5-bis(phenylmethoxy)benzoyl]amino]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=N)N1CCc2ccccc2C1\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][P][C][N][C][C][C][N][C][C][Branch1][Ring2][C][Ring1][Branch2][O][Ring1][#Branch1][C][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[2-[(8s)-2,6,7,8-tetrahydro-1h-cyclopenta[e][1]benzoxol-8-yl]ethyl]propanamide\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccc2cn[nH]c2c1\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][N]\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cnc(nc1NC(C)C)c2ccccn2\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C@H1][C][C][C][N][Ring1][Branch1][C][C][C][O][C][=C][C][=C][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=N][C][=N][C][Ring2][Ring1][Branch2][=C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H24F3N5O5/c1-15(2)20(21(35)25(26,27)28)32-19(34)13-33-22(17-9-6-10-29-11-17)30-12-18(23(33)36)31-24(37)38-14-16-7-4-3-5-8-16/h3-12,15,20H,13-14H2,1-2H3,(H,31,37)(H,32,34)\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H8N2O2/c13-9-7-3-1-2-4-8(7)11-10-12(9)5-6-14-10/h1-4H,5-6H2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCNC(=O)c1nnc2c(cccc2c1N)c3cnc(OC)nc3OC\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(Cn2cc3N(CC(C)C)C(=O)N(C)C(=O)c3c2)cc1\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][\\\\C][=C][\\\\C@H1][Branch1][#Branch2][C][C@@H1][C][C][N][C][Ring1][Branch1][=O][N][C][=Branch1][C][=O][C@@H1][Branch2][Ring1][=N][C][C][=Branch1][C][=O][C@@H1][Branch1][S][N][C][=Branch1][C][=O][C][C][=C][Branch1][C][C][O][N][=Ring1][=Branch1][C][Branch1][C][C][C][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9NO2S/c12-10(13)6-14-9-5-11-8-4-2-1-3-7(8)9/h1-5,11H,6H2,(H,12,13)\\n\",\n        \"output\": \" -1.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][N][C][=N][C][C][N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (8r,9s,10r,13s,14s,17r)-10,13-dimethylspiro[2,8,9,11,12,14,15,16-octahydro-1h-cyclopenta[a]phenanthrene-17,5'-oxolane]-2',3-dione\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][C][C][Branch1][Ring2][C][Ring1][#Branch1][C][C][Branch1][C][N][Branch1][Ring2][C][Ring1][=Branch2][C][Ring1][N]\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H16ClF3N2O5S/c1-12(22,13(15,16)17)11(21)19-10-4-3-8(7-9(10)14)25(23,24)18-5-2-6-20/h3-4,7,18,20,22H,2,5-6H2,1H3,(H,19,21)/t12-/m1/s1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cccc(C(=O)N)c1NC(=O)c2ccccc2\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)\\n\",\n        \"output\": \" -0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O[C@@H](CNCCCSCCNCCc1cccc(Cl)c1Cl)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[[4-[(2,5-dichlorophenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][Branch1][P][C][C][C][=C][C][=Branch1][C][=O][C][C][C][Ring1][O][Ring1][#Branch1][C][C][Ring1][S][C][C][C][Ring2][Ring1][Ring1][O]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][Ring1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][N][Branch2][Ring1][C][C][C][C][N][N][=C][C][=C][C][=C][N][Ring1][=Branch1][C][Ring1][=Branch2][=O][C][C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1ccc2c(c1)c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-pyridin-4-ylnaphthalene-1-carboxamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=N][C][=Branch2][Ring1][C][=C][Ring1][Branch1][S][C][=N][C][=N][C][N][=C][NH1][C][Ring1][=Branch2][=Ring1][Branch1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 0.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][=C][N][=C][C][=C][C][=N][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H16FN3OS/c1-27(26)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](CO)Nc1nc(SCc2ccccc2F)nc3nc(N)sc13\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinazolin-4-amine\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" rat\\n\",\n        \"output\": \" rat is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(5-bromothiophen-2-yl)sulfonyl-n-(2-methylphenyl)propanamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H26ClN3O/c1-3-22(11-12-23)10-4-5-14(2)21-17-8-9-20-18-13-15(19)6-7-16(17)18/h6-9,13-14,23H,3-5,10-12H2,1-2H3,(H,20,21)\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccccc3)c2cc1OC\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][S][C][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=Ring1][=N][C][=Ring1][S][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H21N3O2/c1-23-16-7-10-19-17(13-16)20-15-8-11-21(12-9-15)18(22)14-5-3-2-4-6-14/h2-7,10,13,15H,8-9,11-12H2,1H3,(H,19,20)\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H24N4O4S2/c1-3-25(4-2)32(28,29)18-11-9-17(10-12-18)21-23-24-22(30-21)31-15-20(27)26-14-13-16-7-5-6-8-19(16)26/h5-12H,3-4,13-15H2,1-2H3\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (3r)-1-[4,4-bis(3-methylthiophen-2-yl)but-3-enyl]piperidine-3-carboxylic acid\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" child\\n\",\n        \"output\": \" child is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" methyl 4-[(3,4,5-trimethoxybenzoyl)amino]benzoate\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3,4-dichlorophenyl)-4-[(3r)-1-ethylpiperidine-3-carbonyl]piperazine-1-carboxamide\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Br][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H21ClF3N3O5S/c1-15(25,16(18,19)20)14(24)22-13-3-2-11(10-12(13)17)29(26,27)21-4-5-23-6-8-28-9-7-23/h2-3,10,21,25H,4-9H2,1H3,(H,22,24)/t15-/m1/s1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][N][Branch1][Ring2][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" N(c1ccccc1)c2ccnc3ccccc23\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H15NO4/c1-12-16(11-17(24-12)13-6-3-2-4-7-13)18(21)20-15-9-5-8-14(10-15)19(22)23/h2-11H,1H3,(H,20,21)(H,22,23)\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][C][=C][Branch1][N][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-dimethylamino-3-[4-[[4-[(2-fluoro-5-methylphenyl)amino]pyrimidin-2-yl]amino]phenoxy]propan-2-ol\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H9ClN2O/c13-9-4-3-5-10(8-9)15-12(16)11-6-1-2-7-14-11/h1-8H,(H,15,16)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20N2O4S/c1-23-13-6-7-14-17(11-13)26-19(20-14)21-18(22)9-5-12-4-8-15(24-2)16(10-12)25-3/h4,6-8,10-11H,5,9H2,1-3H3,(H,20,21,22)\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1cc(c(cn1)c2cc(nc(n2)N3CCOCC3)N4CCOCC4)C(F)(F)F\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][Branch2][C][C][=N][C][=C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][=C][Ring1][#Branch2][C][=C][Ring2][Ring1][Branch1][O][C]\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-(cyclopentylamino)-1-(2-fluorophenyl)-2-oxoethyl]-n-(2,4-dimethoxyphenyl)furan-2-carboxamide\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(2,4-difluorophenyl)-1,3-bis(1,2,4-triazol-1-yl)propan-2-ol\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (3s)-n-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-hydroxy-5-[1-hydroxy-2-(4-phenylbutan-2-ylamino)ethyl]benzamide\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[1-(1-adamantyl)ethylamino]-1-(4-nitrophenyl)ethanol\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ncc(nc1C(=O)Nc2cccnc2)c3ccc(cc3)S(=O)(=O)N4CCOCC4\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[1-[3,3-di(phenyl)propyl]piperidin-4-yl]-3h-isoindol-1-one\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H10N2OS/c14-10(13-11-12-6-7-15-11)8-9-4-2-1-3-5-9/h1-7H,8H2,(H,12,13,14)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C[C@H](NC(=O)N1CCOCC1)C(=O)N[C@@H](CCc2ccccc2)\\\\C=C\\\\S(=O)(=O)c3ccccc3\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(N(C(C(=O)NC2CCCC2)c3ccccc3F)C(=O)c4occc4)c(OC)c1\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3,7-dimethyl-1-(5-oxohexyl)purine-2,6-dione\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2-methoxy-5-sulfamoylbenzamide\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14N2O4/c1-10(12-11,9(15)16)5-6-2-3-7(13)8(14)4-6/h2-4,12-14H,5,11H2,1H3,(H,15,16)/t10-/m0/s1\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][C][Branch1][Branch1][C][C][Ring1][#Branch1][N][C][=Branch1][C][=O][C@@H1][Branch1][C][N][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COCCNCc1ccc(cc1)c2cc(C(=O)N)c(NC(=O)N)s2\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(C1CCN(CC[C@@H](c2ccc(F)cc2)c3ccc(cc3)S(=O)(=O)C)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H29N5O6S/c1-27(2,3)18-10-12-19(13-11-18)39(34,35)32-23-22(38-21-9-6-5-8-20(21)36-4)26(37-17-16-33)31-25(30-23)24-28-14-7-15-29-24/h5-15,33H,16-17H2,1-4H3,(H,30,31,32)\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=N][C][Branch1][C][Cl][=C][N][=C][Ring1][#Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H23NO2/c1-15-3-7-17(8-4-15)20(23)18-11-13-22(14-12-18)21(24)19-9-5-16(2)6-10-19/h3-10,18H,11-14H2,1-2H3\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=Branch1][Branch1][=N][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch2][Ring1][Branch2][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H24N2O5/c1-12(2)11-26-16-7-15(8-17(9-16)27-13(3)4)19(23)22-18-6-5-14(10-21-18)20(24)25/h5-10,12-13H,11H2,1-4H3,(H,24,25)(H,21,22,23)\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch2][Ring1][P][N][C][=Branch1][C][=O][N][C][C][C][C][Branch1][C][O][Branch1][Ring2][C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H28N2/c1-20(2)14-9-15-21-18-12-6-4-3-5-10-16(18)17-11-7-8-13-19(17)21/h7-8,11,13H,3-6,9-10,12,14-15H2,1-2H3\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2-(1h-benzimidazol-2-yl)ethyl]-1h-benzimidazole\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H18ClF3N2O3/c1-15(25,16(18,19)20)14(24)21-12-6-5-10(9-11(12)17)13(23)22-7-3-2-4-8-22/h5-6,9,25H,2-4,7-8H2,1H3,(H,21,24)/t15-/m1/s1\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][Branch1][=C][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCNC1=CC=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccccc2\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCC[C@@H]([C@H]1C(=O)Nc2ccc(OCc3cc(C)nc4ccccc34)cc2)C(=O)NO\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(phenylmethyl)-3,8-diazabicyclo[3.2.1]octane-2,4-dione\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][=C][Ring1][=N]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][S][C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(OC)c(cc1NC(=O)C)S(=O)(=O)N2C(C)Cc3ccccc23\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN(C)C\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(C)c(c(C)c1)S(=O)(=O)N(C)CCOCC(=O)N2CCC(CC2)C3CCN(C)CC3\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(4-chlorophenyl)methyl]-4-methylpyridin-2-amine\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C6H11NO/c8-6-4-2-1-3-5-7-6/h1-5H2,(H,7,8)\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H9N3O/c1-7-6-10-12-13-11(15)14(10)9-5-3-2-4-8(7)9/h2-6H,1H3,(H,13,15)\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H19N5O2/c1-3-8-21-18(24)17-15(19)12-6-4-5-11(16(12)22-23-17)13-10-20-9-7-14(13)25-2/h4-7,9-10H,3,8H2,1-2H3,(H2,19,22)(H,21,24)\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[(3,4-dimethoxyphenyl)methyl]-1,3,4,9-tetrahydropyrido[3,4-b]indole\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H18N2O2/c1-3-17-19-16-8-6-5-7-15(16)18(21)20(17)13-9-11-14(12-10-13)22-4-2/h5-12H,3-4H2,1-2H3\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-ethoxyphenyl)-3-(2,5,7-trimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)propanamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H28N6O2/c1-23(2,3)29-22(30)26-17-11-9-16(10-12-17)19-18(27-21(25)28-20(19)24)14-31-13-15-7-5-4-6-8-15/h4-12H,13-14H2,1-3H3,(H2,26,29,30)(H4,24,25,27,28)\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)CCNC(=O)c1cc(Cl)c(N)cc1OC\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1)C(NC(=O)CC2CCN(Cc3ccn(c3)c4ccc(cc4)C(F)(F)F)CC2)C5=CNC(=O)C=C5\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][Branch1][P][C][=Branch1][C][=O][N][C][C][C][C][Branch1][C][C][C][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1,1-dioxo-4-(4-phenylpiperidin-1-yl)thiolan-3-ol\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ncc([nH]1)c2ccc(F)cc2\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" [O-][N+](=O)c1ccc2OC(CN(c2c1)c3cccc[n+]3[O-])(C(F)F)C(F)F\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C@@H1][C][C][C@H1][Ring1][Branch1][C][C@H1][Branch1][Ring2][C][Ring1][#Branch1][O][C][=Branch1][C][=O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][\\\\C][=Branch1][#Branch2][=C][/C][N][C][C][C][C][Ring1][Branch1][\\\\C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [1-(4-methylbenzoyl)piperidin-4-yl]-(4-methylphenyl)methanone\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H17NS/c1-9(2)13-14-11(7-8-15-13)10-5-3-4-6-12(10)16-14/h3-6,9,13,15H,7-8H2,1-2H3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-3-[4-[3-(pyridin-2-ylamino)propoxy]phenyl]-2-[(2,4,6-trimethylbenzoyl)amino]propanoic acid\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H14N2O/c1-10-6-7-14-13(8-10)15-9-11-4-2-3-5-12(11)16/h2-8,16H,9H2,1H3,(H,14,15)\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" [O-]c1c2c(nn1c3ccc(Cl)cc3)c4ccccc4c[n+]2Cc5ccccc5\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)c2ccccc2\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H7NO3/c12-8-3-1-2-6-4-5-7(10(13)14)11-9(6)8/h1-5,12H,(H,13,14)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNc1ncc(s1)C(=O)c2ccccc2\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H15N5O5/c13-9-6-4(10(14)21)1-17(11(6)16-3-15-9)12-8(20)7(19)5(2-18)22-12/h1,3,5,7-8,12,18-20H,2H2,(H2,14,21)(H2,13,15,16)/t5-,7-,8-,12-/m1/s1\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" c1ccc2[nH]c(nc2c1)c3cscn3\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCC(C)(COC(=O)N)COC(=O)NC(C)C\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@][C][C][C@H1][C@@H1][Branch2][Ring1][Ring2][C][C][=Branch1][C][=C][C][=C][C][=Branch1][C][=O][C][=C][C@][Ring1][N][Ring1][#Branch1][C][C@@H1][Ring1][P][C][C][C][Ring2][Ring1][Ring2][=O]\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H27F3N4O7/c1-13(2)19(21(34)25(26,27)28)29-17(33)11-31-16(14-8-6-5-7-9-14)10-15-20(23(31)36)30-24(37)32(22(15)35)12-18(38-3)39-4/h5-10,13,18-19H,11-12H2,1-4H3,(H,29,33)(H,30,37)\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][N][C][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H19NO6/c1-22-14-9-12(10-15(23-2)16(14)24-3)17(20)19-13-7-5-11(6-8-13)18(21)25-4/h5-10H,1-4H3,(H,19,20)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][C][C@H1][Branch1][Ring2][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@H](Oc1cccc2ncnc(Nc3ccc4c(cnn4Cc5ccccn5)c3)c12)C(=O)N6CCOCC6\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCNC(=O)c1ccc(C)c(c1)N2C=Nc3ccc(cc3C2=O)N4CCN(C)CC4\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H26ClNO/c1-21(17-7-4-3-5-8-17,18-10-12-19(22)13-11-18)24-16-14-20-9-6-15-23(20)2/h3-5,7-8,10-13,20H,6,9,14-16H2,1-2H3/t20-,21-/m1/s1\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H22N2O6/c1-15(14-29-2)30-19-10-17(11-20(12-19)31-18-6-4-3-5-7-18)22(26)25-21-9-8-16(13-24-21)23(27)28/h3-13,15H,14H2,1-2H3,(H,27,28)(H,24,25,26)/t15-/m0/s1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(5-chloro-2-methoxyphenyl)-3-pyrazin-2-ylurea\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(3,4,5-trimethoxyphenyl)methyl]-1h-benzimidazol-2-amine\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H19NO4S2/c1-12-4-9-17-16(10-12)19(13(2)20(17)11-18(21)22)25-14-5-7-15(8-6-14)26(3,23)24/h4-10H,11H2,1-3H3,(H,21,22)\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1][C][Ring1][P]\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H17NO/c1-8-5-4-6-9(2)11(8)13-7-10(3)12/h4-6,10H,7,12H2,1-3H3/t10-/m0/s1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring2][=Branch2][C][=Branch1][C][=O][N][Branch1][=C][C][C@H1][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][P][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccccc2)NC(=O)OCC(F)(F)F)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)c1ccc2C=C(C(=O)C)C(=O)Oc2c1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1nc(nc(N2CCCC2)c1Cl)c3ccccn3\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-morpholin-4-yl-6-(phenylsulfonylmethyl)-2-pyridin-2-ylpyrimidine\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H12F9NO3S/c18-14(19,20)10-27(31(29,30)13-4-2-1-3-5-13)12-8-6-11(7-9-12)15(28,16(21,22)23)17(24,25)26/h1-9,28H,10H2\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][N][Branch1][S][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O][C][=N][C][=N][C][Branch1][C][N][=C][Ring2][Ring1][Ring1][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(phenylmethyl)-2h-phthalazin-1-one\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2nc(CCNCCCO)ccc2c1NC(=O)CC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,7-diaminophenanthrene-9,10-dione\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(3s,4r)-3,4-dihydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)-6-(quinolin-4-ylmethyl)thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H24ClN3O5/c24-15-6-7-16-14(9-15)10-18(25-16)22(31)26-17(8-13-4-2-1-3-5-13)21(30)23(32)27-11-19(28)20(29)12-27/h1-7,9-10,17,19-21,25,28-30H,8,11-12H2,(H,26,31)/t17-,19-,20+,21+/m0/s1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H24N6O3/c1-16-3-4-17(23(31)26-22-7-12-33-27-22)13-21(16)30-15-25-20-6-5-18(14-19(20)24(30)32)29-10-8-28(2)9-11-29/h3-7,12-15H,8-11H2,1-2H3,(H,26,27,31)\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][N][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C@][C][N][C][C@H1][Ring1][Branch1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1h-indazole\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][Branch1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring2][Branch2][C][C][=C][C][=C][C][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][Branch1][Ring1][C][O][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(O)(C(=O)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1oc(cc1C(=O)Nc2cccc(c2)C(=O)O)c3ccccc3\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (e)-n-[4-[(3-chloro-4-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]-4-piperidin-1-ylbut-2-enamide\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2,2-dichloro-n-[(1r,2r)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)c1ncnc2c1ncn2Cc3c(Cl)cccc3Cl\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1CN(C(=O)c2ccccc2)c3ccccc3NC1=O\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][#C][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][O][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc2cn[nH]c2c1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC1=CC=C2C(=CC1=O)C(CCc3cc(OC)c(OC)c(OC)c23)NC(=O)C\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C31H36F2N2O3S/c1-3-35(31(36)22-23-4-14-29(15-5-23)39(2,37)38)28-16-19-34(20-17-28)21-18-30(24-6-10-26(32)11-7-24)25-8-12-27(33)13-9-25/h4-15,28,30H,3,16-22H2,1-2H3\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(ccc1OCCN2CCCC2)N3C=Nc4cc(sc4C3=O)c5ccc(Cl)cc5\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-methyl-1-(2-methylpropyl)-5-(pyrrolidine-1-carbonyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(CN2CCC2)cnc1c3ccc(cc3)C(=O)Nc4ccccc4N\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(\\\\C=C/2\\\\CCc3ccccc3C2=O)cc1CN4CCOCC4\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch2][Ring2][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch2][Ring2][=Branch1][C][=Branch1][C][=O][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][Branch2][Ring2][C][N][Branch1][=N][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" [O-][N+](=O)c1ccc2C(=O)C(=O)c3ccccc3c2c1\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-diethyl-4-(phenyl-piperidin-4-ylidenemethyl)benzamide\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@H](Oc1cc(cnc1N)c2cnn(c2)C3CCNCC3)c4c(Cl)ccc(F)c4Cl\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" jute\\n\",\n        \"output\": \" jute is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H10N2OS/c1-2-12-6-3-4-7-8(5-6)13-9(10)11-7/h3-5H,2H2,1H3,(H2,10,11)\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][N][C][C][C][Ring1][#Branch1][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)[C@H](Cc1ccccc1)NC(=O)c2cc3cc(F)ccc3[nH]2\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C1CN2CCC1C(C2)c3oc(nn3)c4oc(cc4)c5cccnc5\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Ring1][O][N][Ring2][Ring1][=Branch1][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][Branch2][Ring2][Ring2][C][C][C][O][C][=C][Branch1][C][C][C][=C][Branch1][=Branch1][C][=C][Ring1][#Branch1][C][C][=N][O][C][=Branch1][Ring2][=N][Ring1][Branch1][C][Branch1][C][F][Branch1][C][F][F][O][N][=Ring2][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H15N5O2/c1-21-10-3-8(4-11(6-10)22-2)12-5-9-7-18-15(17)20-14(9)19-13(12)16/h3-7H,1-2H3,(H4,16,17,18,19,20)\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[3-[4-chloro-3-(cycloheptylmethylcarbamoyl)phenyl]pyridin-2-yl]piperidine-4-carboxylic acid\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][C][=C][Branch2][Ring2][#Branch1][N][C@H1][Branch1][Branch1][S][C][Ring1][=Branch1][C@H1][Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][\\\\C][=Branch1][Ring2][=N][/O][C][\\\\C][=C][S][C][Branch1][C][N][=N][Ring1][=Branch1][C][Ring2][Ring1][Ring1][=O][C][=Branch1][C][=O][O][C][Branch1][C][C][O][C][=Branch1][C][=O][O][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CS(=O)(=O)c1ccc(cc1Cl)[C@@H](CC2CCCC2)C(=O)Nc3cnc(cn3)[C@H](O)CO\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[[(1s)-1-(2-fluorophenyl)ethyl]amino]-5-methyl-5-(trifluoromethyl)-1,3-thiazol-4-one\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][NH1][C][=C][Branch1][C][C][N][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[4-[[4-(benzoylamino)-9,10-dioxoanthracen-1-yl]amino]-9,10-dioxoanthracen-1-yl]benzamide\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[1-[(3r)-3-(3-chlorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][#Branch1][C][N][Branch1][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][N][Ring1][=Branch2][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][Branch1][N][C][C][Branch1][C][C][Branch1][C][C][C][Ring1][Branch2][O][C][=Branch1][C][=O][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-ethyl-1,3-di(phenyl)urea\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(CCCOc2c(C)cc(cc2C)c3noc(n3)C(F)(F)F)on1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H26FNO4/c1-3-26-22-6-4-17(12-18(22)5-7-23(26)27)16-30-21-14-19(13-20(25)15-21)24(28-2)8-10-29-11-9-24/h4-7,12-15H,3,8-11,16H2,1-2H3\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[6-[(3,4-dimethoxybenzoyl)amino]pyridin-2-yl]-3,4-dimethoxybenzamide\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(cc1C(=O)NCC2CCCCC2)N3N=CC(=O)NC3=O\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][C][Ring1][=Branch1][C][Branch1][Ring2][C][Ring1][=Branch1][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][O][C][=Branch1][Branch1][=C][C][=Ring1][Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-1-(2,6-dimethylphenoxy)propan-2-amine\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][N][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=Ring1][Branch2][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6,7-dimethoxy-4-[(3r)-3-quinoxalin-2-yloxypyrrolidin-1-yl]quinazoline\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)NCC(O)COc1ccc(COCCOC(C)C)cc1\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OCC(CO)NC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(COc1ccccc1)N2CCOCC2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@@H](C(=O)NCCN1CCCC1)c2ccc(OS(=O)(=O)C(F)(F)F)cc2\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][S][C][=N][C][Branch1][C][N][=C][N][=C][N][Branch1][S][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O][C][Ring1][=C][=N][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)COc1ccc(O)cc1\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc(N)c2cc(Br)ccc2n1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H20N2O2/c16-11-13(17)10-14-6-8-15(9-7-14)12-4-2-1-3-5-12/h1-5,13,16-17H,6-11H2\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1[nH]c(C(=O)NC2CCN(CC2)c3ncc(s3)C(=O)O)c(Cl)c1Cl\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H24ClN5O4/c25-17-4-2-16(3-5-17)24(10-1-11-24)22(32)27-23-29-28-21(34-23)20(31)26-18-6-8-19(9-7-18)30-12-14-33-15-13-30/h2-9H,1,10-15H2,(H,26,31)(H,27,29,32)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" cicada\\n\",\n        \"output\": \" cicada is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H14N4O4/c1-12-8-7(9(17)13(2)10(12)18)14(5-11-8)3-6(16)4-15/h5-6,15-16H,3-4H2,1-2H3\\n\",\n        \"output\": \" -1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" beetle\\n\",\n        \"output\": \" beetle is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H19F2N7O/c1-19(2,3)13-8-15-24-25-17(12-7-11(20)5-6-14(12)21)28(15)26-18(13)29-9-16-22-10-23-27(16)4/h5-8,10H,9H2,1-4H3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)N2NC(=O)c3cccnc23\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)n1c2ccccc2c3cc(NC(=O)N4CCOCC4)ccc13\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H10O5/c1-2-16-11(14)9-5-7-3-4-8(13)6-10(7)17-12(9)15/h3-6,13H,2H2,1H3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNC(=O)c1ccc(Nc2ncc(F)c(n2)c3cnc(C)n3C(C)C)cc1F\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" daniel\\n\",\n        \"output\": \" daniel is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-methylsulfanyl-n-(1,3-thiazol-2-yl)pyridine-3-carboxamide\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15+,16?\\n\",\n        \"output\": \" -0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)CNCCNc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1oncc1C(=O)Nc2ccc(cc2)C(F)(F)F\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-methylphenyl)-2,1,3-benzoxadiazole-7-sulfonamide\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H10N2OS/c12-8-6-9(15-10(8)11(13)14)7-4-2-1-3-5-7/h1-6H,12H2,(H2,13,14)\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-1-(tert-butylamino)-3-[(4-morpholin-4-yl-1,2,5-thiadiazol-3-yl)oxy]propan-2-ol\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)c1ccccc1Cc2cc(C(=O)Nc3ccc(cc3)S(=O)(=O)c4ccccc4C(C)(C)C)c(O)c(O)c2O\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(2,3-dihydro-1,4-benzodioxin-2-ylmethyl)-3-hydroxythieno[2,3-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)c2nc(CCOc3ccc(C[C@H](Nc4ccccc4C(=O)c5ccccc5)C(=O)O)cc3)c(C)s2\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][N][C][=C][C][=C][Ring1][Branch1][N][C][C][N][Branch1][#C][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][C][Ring1][S]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-diethylamino-1-phenylpropan-1-one\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H24F3N3O3/c1-4-25-15-10-11-16(14-8-6-5-7-9-14)27(20(15)30)12-17(28)26-18(13(2)3)19(29)21(22,23)24/h5-11,13,18,25H,4,12H2,1-3H3,(H,26,28)\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][=N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-aminophenyl)-4-morpholin-4-ylbenzamide\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)NC[C@@H](O)COc1cccc2ccccc12\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H15NO2/c1-2-4-10(5-3-1)14-9-11-8-12-6-7-13-11/h1-5,11-12H,6-9H2\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1=C(N2[C@H](SC1)[C@H](NC(=O)[C@H](N)c3ccc(O)cc3)C2=O)C(=O)O\\n\",\n        \"output\": \" -0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H25NO/c1-22-18-12-13-19(22)15-20(14-18)23-21(16-8-4-2-5-9-16)17-10-6-3-7-11-17/h2-11,18-21H,12-15H2,1H3/t18-,19+,20+\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])NC(=O)c2cccc3ccccc23\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H12N2/c1-2-6-12(7-3-1)17-15-10-11-16-14-9-5-4-8-13(14)15/h1-11H,(H,16,17)\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H7N3/c8-6-2-1-5-4-9-10-7(5)3-6/h1-4H,8H2,(H,9,10)\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@H1][Branch1][C][O][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch2][Ring1][C][C][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][C@@H1][Ring2][Ring1][#Branch1][Ring2][Ring1][C]\\n\",\n        \"output\": \" -0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][N][Branch1][Branch1][C][C][Ring1][Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-cyclohexyl-1-phenyl-3-pyrrolidin-1-ylpropan-1-ol\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[[5-(3,5-dimethylphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1CCN(Cc2ccc(cc2)c3cc4c(N[C@H](C)c5ccccc5)ncnc4[nH]3)CC1\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nc2nc(cc(n2n1)C(F)(F)F)c3cccs3\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-amino-2-methylsulfanyl-1,3-thiazole-4-carboxamide\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch2][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring1][=N]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27F3N4O5/c1-13(2)18(19(32)23(24,25)26)29-17(31)11-30-20(14(3)4)27-10-16(21(30)33)28-22(34)35-12-15-8-6-5-7-9-15/h5-10,13-14,18H,11-12H2,1-4H3,(H,28,34)(H,29,31)\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)benzamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H17FO3S/c1-12-17(9-13-3-6-15(7-4-13)25(2)24)16-8-5-14(21)10-19(16)18(12)11-20(22)23/h3-10H,11H2,1-2H3,(H,22,23)/b17-9-\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H10Cl2N2O2/c14-10-3-1-8(11(15)5-10)6-17-7-9(13(16)19)2-4-12(17)18/h1-5,7H,6H2,(H2,16,19)\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][NH1][N][=C][Branch1][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][C][=Ring1][=N][C][=C][C][=N][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H20N2OS/c21-18(19-15-12-20-10-8-13(15)9-11-20)17-7-6-16(22-17)14-4-2-1-3-5-14/h1-7,13,15H,8-12H2,(H,19,21)/t15-/m1/s1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H20N2O3/c1-16(24)23(15-17-8-6-7-11-20(17)25-2)19-14-22-13-12-21(19)26-18-9-4-3-5-10-18/h3-14H,15H2,1-2H3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][Branch1][C][C][C][C][O][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H](Nc1ncc(F)c(Nc2cc([nH]n2)C3CC3)n1)c4ncc(F)cn4\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H22F6N2O/c22-20(23,24)17-10-15(11-18(12-17)21(25,26)27)13-30-14-19(16-4-2-1-3-5-16)29-8-6-28-7-9-29/h1-5,10-12,19,28H,6-9,13-14H2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H11N5O/c15-10-7-13-17-18-14(20)19(13)12-6-8(3-4-9(10)12)11-2-1-5-16-11/h1-7,16H,15H2,(H,18,20)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC12CCC3C(CCC4=CC(=O)CCC34C)C1CCC2O\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O]\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=N][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n,n-dimethyl-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" ethyl 2-[2-[(4-chlorophenyl)sulfonylamino]-1,3-thiazol-4-yl]acetate\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H14ClN3O/c18-13-7-5-12(6-8-13)16(22)11-21-15-4-2-1-3-14(15)20-10-9-19-17(20)21/h1-8H,9-11H2\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][S][C][=Ring1][Branch1][C][=Branch2][Ring1][Ring1][=C][C][C][N][C][C][C][C@H1][Branch1][Ring2][C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][S][C][=C][C][=Ring1][Branch1][C]\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=CC(=O)Oc2cc3NCCCc3cc12\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H28N2O3/c1-16-11-13-18(14-12-16)25-23(27)22-19-8-4-5-9-20(19)24(28)26(22)15-17-7-3-6-10-21(17)29-2/h3-10,16,18,22H,11-15H2,1-2H3,(H,25,27)\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H24ClN7O2/c24-18-13-16(6-7-19(18)33-14-17-5-1-2-8-25-17)28-21-20-22(27-15-26-21)29-30-23(20)32-12-11-31-9-3-4-10-31/h1-2,5-8,13,15H,3-4,9-12,14H2,(H2,26,27,28,29,30)\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H41NO2/c1-15-11-24-25(28-14-15)17(3)27(30-24)10-8-20-21-6-5-18-12-19(29)7-9-26(18,4)23(21)13-22(20)16(27)2/h5,15,17,19-21,23-25,28-29H,6-14H2,1-4H3/t15-,17+,19-,20-,21-,23-,24+,25-,26-,27-/m0/s1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-hydroxy-3-(4-hydroxyphenyl)chromen-4-one\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-chloro-n-(6-chloropyridin-3-yl)-4-fluorobenzamide\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1c(NC(=O)Nc2cccc(F)c2Cl)ccc(Cl)c1S(=O)(=O)N3CCNCC3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H10O6/c17-9-4-11(18)15-14(5-9)20-6-10(16(15)19)8-1-2-12-13(3-8)22-7-21-12/h1-6,17-18H,7H2\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-pyridin-3-ylbenzenesulfonamide\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=CN(Cc2ccccc2)C(=O)NC1=O\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][=N][C][C][=Branch1][C][=O][N][Branch1][Ring2][C][C][=C][C][C][C][N][Branch2][Ring1][=Branch1][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch1][C][=C][Ring2][Ring2][C]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H16N4O/c1-3-17(23)21-14-7-8-16-15(10-14)18(20-11-19-16)22-13-6-4-5-12(2)9-13/h3-11H,1H2,2H3,(H,21,23)(H,19,20,22)\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H21ClFN5O2/c1-11(19(23)28)27(2)9-12-7-13-16(8-17(12)29-3)24-10-25-20(13)26-15-6-4-5-14(21)18(15)22/h4-8,10-11H,9H2,1-3H3,(H2,23,28)(H,24,25,26)/t11-/m1/s1\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (3s)-n-methyl-3-naphthalen-1-yloxy-3-thiophen-2-ylpropan-1-amine\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O[C@H](C[C@H](O)\\\\C=C\\\\c1c(nc2ccccc2c1c3ccc(F)cc3)C4CC4)CC(=O)O\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(1-adamantyl)-n-[2-[2-(3-hydroxypropylamino)ethyl]-6-methylquinolin-5-yl]acetamide\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [6-(5-chloropyridin-2-yl)-5-oxo-7h-pyrrolo[3,4-b]pyrazin-7-yl] 4-methylpiperazine-1-carboxylate\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][N][=C][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H23N5O2/c1-5-26-16-8-6-15(7-9-16)22-18(25)11-10-17-12(2)20-19-21-14(4)23-24(19)13(17)3/h6-9H,5,10-11H2,1-4H3,(H,22,25)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(4-phenylpyrimidin-2-yl)amino]benzenesulfonamide\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H12ClN3O3S/c21-11-5-6-13-14(8-11)22-17-16(18(13)25)20(27)24(23-19(17)26)9-12-7-10-3-1-2-4-15(10)28-12/h1-8H,9H2,(H,22,25)(H,23,26)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H21FN4O/c21-16-6-8-17(9-7-16)25-20(22)19(15-4-2-1-3-5-15)18(23-25)14-24-10-12-26-13-11-24/h1-9H,10-14,22H2\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][=C][Branch1][N][N][=C][C][=C][C][=C][N][Ring1][#Branch2][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1NC=Nc2scc(c3cccs3)c12\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C@H1][Branch2][Ring2][=Branch2][N][C][C][N][Branch1][=Branch1][C][C@@H1][Ring1][=Branch1][C][C][Branch1][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][=C][N][=C][Ring1][#Branch1][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H23N3O4/c1-2-22-15(21)12-7-9-13(10-8-12)23-14(20)6-4-3-5-11-19-16(17)18/h7-10H,2-6,11H2,1H3,(H4,17,18,19)\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H18FN3O3/c1-2-19-9-11(16(22)23)15(21)10-7-12(17)14(8-13(10)19)20-5-3-18-4-6-20/h7-9,18H,2-6H2,1H3,(H,22,23)\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCCn1c2CCCCCCc2c3ccccc13\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl n-[2-amino-6-[(4-fluorophenyl)methylamino]pyridin-3-yl]carbamate\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H22ClNO2/c1-23(2)13-19-22(15-6-4-3-5-7-15)21(16-8-10-17(24)11-9-16)18(12-20(26)27)25(19)14-23/h3-11H,12-14H2,1-2H3,(H,26,27)\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccccc1N2CCN(CC2)C(=O)NC3CCCCC3\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H10O4/c16-11-3-1-9(2-4-11)13-8-10-7-12(17)5-6-14(10)19-15(13)18/h1-8,16-17H\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H15N3O2/c23-18(14-8-3-1-4-9-14)21-16-12-7-13-17(20-16)22-19(24)15-10-5-2-6-11-15/h1-13H,(H2,20,21,22,23,24)\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)CCC(=O)Nc1ccc2C(=O)C(=O)c3ccccc3c2c1\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(1h-indol-4-yloxy)-3-(propan-2-ylamino)propan-2-ol\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][=N][O][C][Branch1][C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][C][C@@H1][Ring1][Branch1][C][C][O][C@][Branch1][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-methyl-6,7,8,9-tetrahydropyrano[5,6-g]quinolin-2-one\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H7N3S/c9-8-10-4-3-6(11-8)7-2-1-5-12-7/h1-5H,(H2,9,10,11)\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H22N4O2/c1-17-8-10-18(11-9-17)22-19-5-2-3-6-20(19)23(26-25-22)27-12-14-28(15-13-27)24(29)21-7-4-16-30-21/h2-11,16H,12-15H2,1H3\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H33N7O3/c1-19-5-6-21(29-25(34)20-7-9-27-24(17-20)33-12-15-35-16-13-33)18-22(19)30-23-8-10-28-26(31-23)36-14-4-11-32(2)3/h5-10,17-18H,4,11-16H2,1-3H3,(H,29,34)(H,28,30,31)\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-3-(3,4-dihydroxyphenyl)-2-hydrazinyl-2-methylpropanoic acid\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-morpholin-4-yl-8-phenylchromen-4-one\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)[C@H](N)C(=O)OCCOCn1cnc2C(=O)N=C(N)Nc12\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)CSc1c[nH]c2ccccc12\\n\",\n        \"output\": \" -1.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Ring1][C@@H1][Branch1][C][O][C@@H1][C][C@H1][C][C][N][Ring1][=Branch1][C][C@@H1][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][#Branch2][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Ring1][P][=O]\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H25ClN4O3/c1-27-8-6-14(7-9-27)30-20-12-16(29-3)11-19-21(20)22(25-13-24-19)26-18-10-15(28-2)4-5-17(18)23/h4-5,10-14H,6-9H2,1-3H3,(H,24,25,26)\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][Branch1][O][N][C][C][C][C][N][C][C][Ring1][=Branch1][N][=C][C][=C][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)CCN1C(=O)CN=C(c2ccccc2F)c3cc(Cl)ccc13\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" knot\\n\",\n        \"output\": \" knot is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]-3-[2-(4-methylpiperazin-1-yl)ethoxy]-1h-pyrazolo[4,5-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-amino-n-(2,6-dimethylphenyl)propanamide\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C28H24N2O6/c1-35-25-15-17(11-13-23(25)29-21-9-5-3-7-19(21)27(31)32)18-12-14-24(26(16-18)36-2)30-22-10-6-4-8-20(22)28(33)34/h3-16,29-30H,1-2H3,(H,31,32)(H,33,34)\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H8ClN3O2S/c1-14-10(16)13-9(17-14)12-8(15)6-3-2-4-7(11)5-6/h2-5H,1H3,(H,12,13,15,16)\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@@H1][Branch1][C][N][C][O][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(9,10-dioxophenanthren-2-yl)-2-(phenylmethoxy)acetamide\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][#Branch1][C][N][Branch1][C][C][C][C][Branch1][C][O][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=C]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-2-[[2-amino-5-[(2-fluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][Ring2][C][C][Cl][C][C][Cl]\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(CC(C)(C)NC[C@H](O)c2cc(O)cc3NC(=O)COc23)cc1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3c(Cl)nccc3n1CC(=O)O\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[(2-chlorophenyl)methyl]-6,7-dihydro-4h-thieno[3,2-c]pyridine\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(Sc2c(C)n(CC(=O)O)c3ccc(C)cc23)cc1\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H26Cl3N3O4S/c24-16-1-4-20(5-2-16)34(31,32)27-23(30)29-11-7-17(8-12-29)28-13-9-18(10-14-28)33-19-3-6-21(25)22(26)15-19/h1-6,15,17-18H,7-14H2,(H,27,30)\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C@@H1][C][C][Branch2][Ring1][S][C][C][N][Branch2][Ring1][Branch1][C][C][=C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=C][Ring1][=N][C][C][Ring2][Ring1][Ring2][C][=C][C][=C][C][=C][Ring2][Ring1][N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" disease\\n\",\n        \"output\": \" disease is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" hood\\n\",\n        \"output\": \" hood is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-n-(4-methyl-1,3-thiazol-2-yl)-5-[(4-methyl-1,2,4-triazol-3-yl)sulfanyl]benzamide\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (4-chlorophenyl)-[1-(4-methylbenzoyl)piperidin-4-yl]methanone\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H19NO/c19-17(16-12-5-2-6-13-16)18-14-8-7-11-15-9-3-1-4-10-15/h1-6,9-10,12-13H,7-8,11,14H2,(H,18,19)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H16ClNO2/c21-18-12-6-4-8-15(18)14-22-20(23)17-11-5-7-13-19(17)24-16-9-2-1-3-10-16/h1-13H,14H2,(H,22,23)\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][N][Branch1][N][Se][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccs2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H9FO4/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,17-18H\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][N][C][=C][C][=C][Ring1][Branch1][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][Branch2][Ring1][=C][C][=Branch2][Ring1][Ring1][=N][C][=C][Ring1][=Branch1][C][=N][N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][=C][C][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Ring1][O][C][=N][C][C][Branch1][C][N][=N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][S][C][Branch1][C][N][=N][C][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" fortnight\\n\",\n        \"output\": \" fortnight is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][#Branch2][O][C][C][C][N][C][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(phenylmethyl)quinazolin-4-amine\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=C][Branch2][Ring1][C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,5,9-trimethylpyrano[5,6-f][1]benzoxol-7-one\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch2][Ring1][Branch1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=N][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[3-[(2s)-1-methoxypropan-2-yl]oxy-5-(phenoxy)benzoyl]amino]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2-(1-hydroxybutan-2-ylamino)ethylamino]butan-1-ol\\n\",\n        \"output\": \" -1.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][N][C][=Branch1][C][=O][\\\\C][=C][\\\\C][N][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][S][C][N][C][=Branch1][C][=O][C][C][C][C][N][Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CC(c2ccccc2)c3cccc(N)c3C1\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][S][C][=N][C][=N][C][Branch2][Ring1][Ring1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=N][Ring1][=Branch1][=C][Ring2][Ring1][C][C][=Ring2][Ring1][Branch1][C]\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (e,3r,5s)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-dihydroxyhept-6-enoic acid\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" jacket\\n\",\n        \"output\": \" jacket is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" FC(F)(F)c1cc(COCC(N2CCNCC2)c3ccccc3)cc(c1)C(F)(F)F\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)NCc1ccc(CN2CCN(CC2)c3ccccc3)cc1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][C][Ring1][#Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H21FN4O3/c1-4-9-23-20(26)19-17(22)13-7-8-14(21)16(18(13)24-25-19)12-6-5-11(27-2)10-15(12)28-3/h5-8,10H,4,9H2,1-3H3,(H2,22,24)(H,23,26)\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][N][=C][C][=C][C][=Branch1][=Branch1][=N+1][Branch1][C][C][C][C][=C][Ring1][=Branch2][S][C][Ring1][=N][=C][Ring1][P]\\n\",\n        \"output\": \" -0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(furan-2-carbonyl)-1,3-dihydroquinoxalin-2-one\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][O][S][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3,4-dichlorophenyl)-4-[[(3r)-1-(phenylmethyl)piperidin-3-yl]methyl]piperazine-1-carboxamide\\n\",\n        \"output\": \" 4.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H21N3O3/c1-14-17-5-3-4-6-18(17)28-19(14)13-25(2)21(27)10-7-15-11-16-8-9-20(26)24-22(16)23-12-15/h3-7,10-12H,8-9,13H2,1-2H3,(H,23,24,26)/b10-7+\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][O][C][=C][C][N][C][C][C][C][=Ring1][=Branch1][C][=C][Ring1][#C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H10N2O2/c13-11(15)10-7-4-8-14-12(10)16-9-5-2-1-3-6-9/h1-8H,(H2,13,15)\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H9NO4/c16-9-3-1-8(2-4-9)15-13(18)11-6-5-10(17)7-12(11)14(15)19/h1-7,16-17H\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][C][C][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-(aminomethyl)phenyl]-6-(n'-hydroxycarbamimidoyl)-4-(pyrimidin-2-ylamino)naphthalene-2-carboxamide\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(Cl)c(O)c3)c2cc1OC\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-acetyl-8-cyclopentyl-5-methyl-2-[(5-piperazin-1-ylpyridin-2-yl)amino]pyrido[6,5-d]pyrimidin-7-one\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H29Cl2N3O5S/c1-33-18-2-5-21(6-3-18)35(31,32)27-24(30)29-12-8-17(9-13-29)28-14-10-19(11-15-28)34-20-4-7-22(25)23(26)16-20/h2-7,16-17,19H,8-15H2,1H3,(H,27,30)\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring2][Ring1][C][C][Branch1][C][C][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][Branch1][C][O][=C][C][N][C][=Branch1][C][=O][C][O][C][Ring1][N][=Ring1][#Branch1][C][=C][Ring2][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H21NO3/c1-17-12-7-8-13(17)10-14(9-12)20-16(19)15(18)11-5-3-2-4-6-11/h2-6,12-15,18H,7-10H2,1H3/t12-,13+,14+,15?\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1CCN(CC(=O)Nc2ccc(c3cccc4C(=O)C=C(Oc34)N5CCOCC5)c6sc7ccccc7c26)CC1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H10N2S/c1-2-7-5-6(8(9)11)3-4-10-7/h3-5H,2H2,1H3,(H2,9,11)\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-oxo-6-phenyl-3-(pyridin-4-ylmethylcarbamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(F)ccc2c1c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[3-acetyl-4-[2-hydroxy-3-(propan-2-ylamino)propoxy]phenyl]butanamide\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][O][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(N2CCN(CC2)C(=O)COCc3ccccn3)c(Cl)c1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][N][Branch1][Branch2][C][C][C][Ring1][=Branch2][=Ring1][Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H12N2OS/c1-15-10-4-2-9(3-5-10)14-16-12-7-6-11(17)8-13(12)18-14/h2-8,15,17H,1H3\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H21N3O/c1-3-16(4-2)10-9-15-13(17)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10,14H2,1-2H3,(H,15,17)\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C@H1][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H15N3O/c17-13(16-7-5-14-6-8-16)12-9-10-3-1-2-4-11(10)15-12/h1-4,9,14-15H,5-8H2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)C(N1CCC(CN2CCC(CC2)Oc3ccc(Cl)c(Cl)c3)CC1)c4ccccc4\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=N][C][=C][Ring1][=Branch1][N][=C][N][Ring1][Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H22N2O2/c1-10(2)14-15(19)16-12(9-18)8-11-6-4-5-7-13(11)17(14)3/h4-7,10,12,14,18H,8-9H2,1-3H3,(H,16,19)/t12-,14-/m0/s1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-aminophenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-methyl-2-phenylpyrazol-3-amine\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H29F3N4O5/c1-16(2)22(23(35)25(26,27)28)30-21(34)15-32-19(17-6-4-3-5-7-17)9-8-18(24(32)36)29-20(33)14-31-10-12-37-13-11-31/h3-9,16,22H,10-15H2,1-2H3,(H,29,33)(H,30,34)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H28F3N3O3S2/c24-23(25,26)16-4-1-3-15(13-16)7-9-27-8-2-11-33-12-10-28-14-19(31)17-5-6-18(30)20-21(17)34-22(32)29-20/h1,3-6,13,19,27-28,30-31H,2,7-12,14H2,(H,29,32)/t19-/m0/s1\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)N[C@@H]1CC2(CCN(Cc3ccc4[nH]c5ccccc5c4c3)CC2)c6ccccc16\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CC(c2ccc(Cl)cc2)c3ccccc3C1\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)S(=O)(=O)Nc2ccccn2\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H16F2N8/c1-8(14-19-5-10(17)6-20-14)22-16-21-7-11(18)15(24-16)23-13-4-12(25-26-13)9-2-3-9/h4-9H,2-3H2,1H3,(H3,21,22,23,24,25,26)/t8-/m0/s1\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" visitor\\n\",\n        \"output\": \" visitor is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-aminophenyl)-4-[5-(azetidin-1-ylmethyl)-3-methylpyridin-2-yl]benzamide\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H22N4O3/c1-15-10-16(7-8-20(15)30-13-17-6-4-5-9-24-17)27-23-18-11-21(28-2)22(29-3)12-19(18)25-14-26-23/h4-12,14H,13H2,1-3H3,(H,25,26,27)\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1nc(Nc2ncc(s2)C(=O)Nc3c(C)cccc3Cl)cc(n1)N4CCN(CCO)CC4\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(OCC(F)(F)F)ccnc1C[S+]([O-])c2nc3ccccc3[nH]2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][N][C][C@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][Branch2][Ring1][Ring1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][Ring2][Ring1][Ring1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C42H25N3O6/c46-37-25-15-7-9-17-27(25)39(48)35-31(44-41(50)23-11-3-1-4-12-23)21-19-29(33(35)37)43-30-20-22-32(45-42(51)24-13-5-2-6-14-24)36-34(30)38(47)26-16-8-10-18-28(26)40(36)49/h1-22,43H,(H,44,50)(H,45,51)\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H20N6O3/c1-4-8-20-16(25)15-13(19)11-7-5-6-10(14(11)23-24-15)12-9-21-18(27-3)22-17(12)26-2/h5-7,9H,4,8H2,1-3H3,(H2,19,23)(H,20,25)\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(cc1)C2(CCC2)C(=O)Nc3oc(nn3)C(=O)Nc4ccc(cc4)N5CCOCC5\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][C][C][C][C][=Branch1][Ring2][=N][Ring1][#Branch1][N]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-2-amino-3-(4-fluorophenyl)propanoic acid\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccccc1NC(=O)c2ccc(cc2)c3ncc(CN4CCC4)cc3F\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccc(NC(=O)c2cccnc2Oc3ccccc3)cc1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H]1CN(Cc2cc(Cl)ccc2CCC(=O)O)CCN1C(=O)Cc3ccccc3\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [3-(aminomethyl)-5-methylcyclohexyl]methanol\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H28ClN5O/c1-2-30-11-13-31(14-12-30)17-18-15-21(26)24(28-16-18)19-7-9-20(10-8-19)25(32)29-23-6-4-3-5-22(23)27/h3-10,15-16H,2,11-14,17,27H2,1H3,(H,29,32)\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" methyl 2-[5-[(4-fluorophenyl)carbamoyl]pyridin-2-yl]oxyacetate\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" -0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-methoxy-3-(4-methylpiperazin-1-yl)phenyl]-3-methyl-4-pyridin-4-ylbenzamide\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][=C][S][C][=N][C][C][N][Ring1][Branch2][Ring1][Branch1]\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H33ClN2O2/c1-26(2)13-19(27)8-15-3-4-21(24)20(9-15)22(28)25-14-23-10-16-5-17(11-23)7-18(6-16)12-23/h3-4,9,16-19,27H,5-8,10-14H2,1-2H3,(H,25,28)/t16?,17?,18?,19-,23?/m1/s1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(NCc1ccncc1)c2ccc(Oc3ccccc3)cc2\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)sc13\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@]12CC[C@H]3[C@@H](CCc4cc(O)ccc34)[C@@H]1CC[C@@H]2O\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H20ClNO2/c1-14-2-4-17(5-3-14)20(24)22-12-10-16(11-13-22)19(23)15-6-8-18(21)9-7-15/h2-9,16H,10-13H2,1H3\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[3-[(2-chloro-1,3-thiazol-5-yl)methoxy]phenyl]acetamide\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H19ClFN3O2/c19-16-11-15(20)1-2-17(16)22-7-9-23(10-8-22)18(24)13-25-12-14-3-5-21-6-4-14/h1-6,11H,7-10,12-13H2\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" zipper\\n\",\n        \"output\": \" zipper is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(5,6-dimethylthieno[3,2-e]pyrimidin-4-yl)sulfanyl-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-acetamido-3-(4-chlorophenyl)sulfonyl-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][=C][C][C][=Branch1][C][=O][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1C2=COc3cc(O)ccc3C2=O\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)N4CCN(CC4)C(=O)CO)n2\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H22N2O2/c1-15-3-6-17(7-4-15)21-14-19(22(25)24-9-11-26-12-10-24)18-13-16(2)5-8-20(18)23-21/h3-8,13-14H,9-12H2,1-2H3\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][C][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][S][C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C32H33N3O6/c36-30-7-4-8-31(37)34(30)28(16-11-23-9-12-25(13-10-23)32(38)33-19-1-2-20-33)22-41-29-17-14-24(15-18-29)26-5-3-6-27(21-26)35(39)40/h3,5-6,9-10,12-15,17-18,21,28H,1-2,4,7-8,11,16,19-20,22H2\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NS(=O)(=O)c1cc(C(=O)O)c(NCc2occc2)cc1Cl\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3/t12-,15-,17-,18-,19-,20-,21-,22-/m0/s1\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[1-[3,3-bis(4-fluorophenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=Branch1][C][=N][N][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1nc2ccccc2s1\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H16N2O3/c1-12(8-6-4-3-5-7-8)9(15)13-11(17)14(2)10(12)16/h6H,3-5,7H2,1-2H3,(H,13,15,17)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[4-(4-chlorophenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[5-(5-formyl-1-methylpyrrol-3-yl)-5-oxopentoxy]benzoic acid\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][=Branch1][=Branch2][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(6-morpholin-4-ylpyridin-3-yl)-5-(phenylamino)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-n-[1-[2-(4-hydroxypiperidin-1-yl)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H21ClN6O/c20-14-3-1-13(2-4-14)11-23-18(27)19(21)6-9-26(10-7-19)17-15-5-8-22-16(15)24-12-25-17/h1-5,8,12H,6-7,9-11,21H2,(H,23,27)(H,22,24,25)\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][=C][Ring1][O]\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3/t16-/m1/s1\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][N][=C][Branch1][Branch2][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring2][#Branch2][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][#C][Cl]\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1cncc(c1)c2ccc(Cl)c(c2)C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H29N5O2/c1-17-6-7-18(24(31)27-19-4-3-5-19)14-23(17)30-16-26-22-9-8-20(15-21(22)25(30)32)29-12-10-28(2)11-13-29/h6-9,14-16,19H,3-5,10-13H2,1-2H3,(H,27,31)\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][NH1][C][Branch2][Ring1][Branch1][\\\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][\\\\-Ring1][O][Ring1][#Branch1][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][O][N][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N]\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H10ClN3/c13-10-4-1-9(2-5-10)3-6-11-7-8-15-12(14)16-11/h1-8H,(H2,14,15,16)/b6-3+\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H17NO/c1-9(2)7-8-13-11-5-3-10(12)4-6-11/h3-6,9H,7-8,12H2,1-2H3\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(3-methoxyphenyl)sulfonyl-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(2-methylpropyl)-5-prop-2-enyl-1,3-diazinane-2,4,6-trione\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(6-amino-5-chloropyridin-3-yl)-2-chloro-5-[[3-(trifluoromethyl)benzoyl]amino]benzamide\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-chloro-4-(furan-2-carbonyl)-5-phenyl-3,5-dihydro-1h-1,4-benzodiazepin-2-one\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(dimethylaminomethyl)-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C32H38F2N2O5S2/c1-4-36(32(37)19-23-5-9-29(10-6-23)42(2,38)39)28-13-16-35(17-14-28)18-15-31(25-20-26(33)22-27(34)21-25)24-7-11-30(12-8-24)43(3,40)41/h5-12,20-22,28,31H,4,13-19H2,1-3H3/t31-/m1/s1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H8N2O/c15-12-9-5-1-2-6-10(9)13-11-7-3-4-8-14(11)12/h1-8H\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][Branch1][O][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H9ClN2O4/c14-10-6-5-8(16(19)20)7-9(10)13(18)15-11-3-1-2-4-12(11)17/h1-7,17H,(H,15,18)\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][NH1][C][=N][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][Cl]\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" benzo[h]quinoline-5,6-dione\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Branch1][#Branch1][N][=C][Ring1][#Branch2][Ring1][=Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[(4-fluorophenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H22N2O/c1-13-7-9-14(10-8-13)12-18(21)20-17-6-2-5-16-15(17)4-3-11-19-16/h2-6,11,13-14H,7-10,12H2,1H3,(H,20,21)\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(COC(=O)N2CC[C@H](CNc3ncccn3)[C@H](F)C2)cc1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H12O5/c21-11-5-7-15-17(9-11)25-18-10-12(22)6-8-16(18)19(15)13-3-1-2-4-14(13)20(23)24/h1-10,21H,(H,23,24)\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-[3-(2-chlorophenothiazin-10-yl)propyl]piperazin-1-yl]ethyl 4-aminobutanoate\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(Nc1nc(cs1)c2ccccc2)c3cccnc3\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 9-methoxyfuro[3,2-g]chromen-7-one\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc2ncccc2c1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch1][#Branch2][C][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1)C(=O)N2CCC(CC2)C(=O)c3ccc(F)cc3\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][=C][C][O][C][=Branch1][C][=O][N][C][C][C@H1][Branch1][O][C][N][C][=N][C][=C][C][=N][Ring1][=Branch1][C@H1][Branch1][C][F][C][Ring1][#C][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1c(Nc2ccc(nc2C)S(=O)(=O)C)ncnc1OC3CCN(CC3)C(=O)OC(C)C\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1C(=O)NC(C1=O)c2ccccc2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-(8-formyl-1,6,7-trihydroxy-3-methyl-5-propan-2-ylnaphthalen-2-yl)-2,3,8-trihydroxy-6-methyl-4-propan-2-ylnaphthalene-1-carbaldehyde\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" c1ccc(cc1)c2cn3ccccc3n2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][=C][N][=C][C][=C][C][=C][N][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-phenyl-1-benzofuran-2-carboxamide\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H19F3N2O2/c1-14-10-18(15(2)26(14)11-16-6-4-3-5-7-16)19(27)13-25-12-17(21(22,23)24)8-9-20(25)28/h3-10,12H,11,13H2,1-2H3\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch1][P][\\\\C][=C][\\\\C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H11NO5/c16-14(17)9-20-13-7-6-11(15(18)19)8-12(13)10-4-2-1-3-5-10/h1-8H,9H2,(H,16,17)\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-pyridin-3-ylpyrimidin-4-amine\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(NCCSCc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H21N3O/c1-16-22-13-15-23(16)14-12-20(19(21)24,17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-11,13,15H,12,14H2,1H3,(H2,21,24)\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=Branch1][#C][=N][C][Branch1][C][N][=C][Ring1][#Branch1][C][=C][Ring1][O][O][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][C][O][Ring1][Branch1]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCc1nc(N)nc(N)c1c2ccc(Cl)cc2\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H6Cl3N3/c13-7-4-5-8(9(14)6-7)12-17-16-11-3-1-2-10(15)18(11)12/h1-6H\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H29N3O/c1-16(2)24(17(3)4)15-13-21(20(22)25,18-10-6-5-7-11-18)19-12-8-9-14-23-19/h5-12,14,16-17H,13,15H2,1-4H3,(H2,22,25)\\n\",\n        \"output\": \" -0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch2][Ring1][=Branch2][N][C][=N][C][=N][C][=C][C][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][#C][Ring1][O][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H24N4O/c1-2-8-20(27)25-13-15-26(16-14-25)22-19-12-7-6-11-18(19)21(23-24-22)17-9-4-3-5-10-17/h3-7,9-12H,2,8,13-16H2,1H3\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" o5-(2-methoxyethyl) o3-propan-2-yl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H28N4O4S/c1-15(2)13-30-25-22(23(32)28(3)26(30)34)21(24(33)29-11-9-17(31)14-29)20(35-25)12-16-8-10-27-19-7-5-4-6-18(16)19/h4-8,10,15,17,31H,9,11-14H2,1-3H3/t17-/m1/s1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H30ClN3O3/c23-19-2-1-17(25-4-3-24-12-20(27)28)8-18(19)21(29)26-13-22-9-14-5-15(10-22)7-16(6-14)11-22/h1-2,8,14-16,24-25H,3-7,9-13H2,(H,26,29)(H,27,28)\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H38O5/c1-6-25(4,5)24(28)30-21-12-15(2)11-17-8-7-16(3)20(23(17)21)10-9-19-13-18(26)14-22(27)29-19/h7-8,11,15-16,18-21,23,26H,6,9-10,12-14H2,1-5H3/t15-,16-,18+,19+,20-,21-,23-/m0/s1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H29N3O4/c29-17-28-22-14-20(8-11-23(22)30)24(31)15-26-13-12-18-6-9-21(10-7-18)27-16-25(32)19-4-2-1-3-5-19/h1-11,14,17,24-27,30-32H,12-13,15-16H2,(H,28,29)/t24-,25-/m0/s1\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNC(=O)c1ccccc1Sc2ccc3c(\\\\C=C\\\\c4ccccn4)n[nH]c3c2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)c2cc(F)cc3C(=O)C=C(Nc23)C(=O)Nc4ccc(cc4)N5CCOCC5\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc(cc1)c2sc3cc(O)ccc3c2C(=O)c4ccc(OCCN5CCCCC5)cc4\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(5-methyl-1h-pyrazol-3-yl)benzamide\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CSc1ccc(OCc2ccccc2)c(\\\\C=C\\\\c3ccc(cn3)C(=O)O)c1\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H12ClN3O3S/c1-8-4-5-25-12(8)7-21-17(24)13-14(16(23)20-21)19-11-6-9(18)2-3-10(11)15(13)22/h2-6H,7H2,1H3,(H,19,22)(H,20,23)\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch2][Branch1][#Branch1][N][C][=C][Branch2][Ring2][N][C][=N][C][=C][Branch1][C][C][C][=C][Branch1][#Branch1][C][=C][Ring1][O][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=Branch1][C][=O][N][=C][Ring2][Ring2][Ring1]\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C[C@H](CO)Nc1nc(S[C@@H](C)c2ccccc2)nc3NC(=O)Sc13\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNC(=O)c1cc(C(=O)c2ccc(Cl)cc2)c(Br)[nH]1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(oxolan-2-yl)-n-(phenylmethyl)butanamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-oxo-4-[4-(3-thiophen-2-yl-1,2,4-oxadiazol-5-yl)piperidin-1-yl]butanoic acid\\n\",\n        \"output\": \" -1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch2][Ring1][#C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=N][Ring1][P][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s,3s)-n-[[2-methoxy-5-(trifluoromethoxy)phenyl]methyl]-2-phenylpiperidin-3-amine\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch2][Ring1][P][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][C][=C][S][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-fluoro-1h-indazole\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl (3r)-4-[2-(3,4-dichlorophenyl)acetyl]-3-(pyrrolidin-1-ylmethyl)piperazine-1-carboxylate\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[(4-fluorophenyl)methoxy]-2-methylpyran-4-one\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1nnc(s1)S(=O)(=O)N\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H25N7O3S/c1-17(26(34)32-7-9-35-10-8-32)36-23-4-2-3-21-24(23)25(28-15-27-21)31-19-5-6-22-18(11-19)12-30-33(22)13-20-14-37-16-29-20/h2-6,11-12,14-17H,7-10,13H2,1H3,(H,27,28,31)/t17-/m1/s1\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)c1cc2cc(ccc2n1Cc3ccc(Cl)c(Cl)c3)[N+](=O)[O-]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COC(=O)NC1=CN=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccc(F)cc2\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COCCOc1cc2nccc(Nc3cc(O)c(Cl)cc3F)c2cc1OC\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H27N3O3/c1-3-26-21(25)18-5-7-19(8-6-18)27-15-12-17-10-13-24(14-11-17)20-9-4-16(2)22-23-20/h4-9,17H,3,10-15H2,1-2H3\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" methyl n-(6-propylsulfanyl-1h-benzimidazol-2-yl)carbamate\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-amino-2-methyl-n-[(2r)-1-(1-methylsulfonylspiro[2h-indole-3,4'-piperidine]-1'-yl)-1-oxo-3-(phenylmethoxy)propan-2-yl]propanamide\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][S][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][C][=Ring1][#Branch2][C][=Branch1][C][=O][C][=C][C][=C][Branch1][N][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][#C]\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CCNc1cc(nc2cc(nn12)c3ccc(F)cc3)c4ccccc4\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H10F3NO2/c15-14(16,17)9-4-3-5-10(8-9)18-12-7-2-1-6-11(12)13(19)20/h1-8,18H,(H,19,20)\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-propan-2-yl-1,2,3,4-tetrahydro-[1]benzothiolo[2,3-c]pyridine\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)C1=COc2ccccc2C1=O\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H24N4O3S/c1-13(2,3)14-8-10(18)9-20-12-11(15-21-16-12)17-4-6-19-7-5-17/h10,14,18H,4-9H2,1-3H3\\n\",\n        \"output\": \" -0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-hydroxyphenyl)chromen-2-one\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H11N3O/c1-8-7-10(14-13-8)12-11(15)9-5-3-2-4-6-9/h2-7H,1H3,(H2,12,13,14,15)\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" alloy\\n\",\n        \"output\": \" alloy is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(1-adamantyl)-n-(3-methoxy-2-methylphenyl)acetamide\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(1h-indol-3-yl)pyrimidin-2-amine\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][C][=C][N][=C][Branch2][Ring1][N][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Ring2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][C][=Branch2][Ring1][#Branch2][=C][Branch1][P][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][=Branch1][C][=O][O][C][C]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCSc1nc(N[C@@H]2C[C@H]2c3ccccc3)c4nnn([C@@H]5C[C@H](CO)[C@@H](O)[C@H]5O)c4n1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m0/s1\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H29N7O4/c1-36-23-14-21-22(15-24(23)38-11-5-8-34-9-12-37-13-10-34)30-18-31-25(21)32-20-16-28-27(29-17-20)33-26(35)19-6-3-2-4-7-19/h2-4,6-7,14-18H,5,8-13H2,1H3,(H,30,31,32)(H,28,29,33,35)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[5-amino-2-(4-fluorophenyl)-6-oxopyrimidin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C@@][Branch1][C][O][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][Ring1][=C][C][=C][Branch1][=N][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][Branch1][#Branch2][O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][O][S][Ring1][=C]\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C6H5N3S/c7-5-4-1-2-10-6(4)9-3-8-5/h1-3H,(H2,7,8,9)\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[[1-(thiophen-2-ylmethyl)tetrazol-5-yl]methyl]piperazin-1-yl]-1,3-benzothiazole\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1n[nH]c(N)c1Cc2ccc3OCOc3c2\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (1r,5s)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=N][C][Branch1][C][C][=C][Branch1][Ring2][S][Ring1][=Branch1][C][=C][N][=C][Branch1][C][F][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][S][C][Branch1][C][C][=N][C][=Ring1][=Branch1][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 8-[4-(4-pyrimidin-2-ylpiperazin-1-yl)butyl]-8-azaspiro[4.5]decane-7,9-dione\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][C][N][Branch1][Ring1][C][C][C][C][C][C][Branch1][C][O][C][=C][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][Ring1][O]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCNC(=O)c1nnc2c(c(F)ccc2c1N)c3ccc(OC)cc3OC\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][S][C][=C][C][=Ring1][Branch1][Cl]\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" estimate\\n\",\n        \"output\": \" estimate is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN[C@H]1CC[C@@H](c2ccc(Cl)c(Cl)c2)c3ccccc13\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" truck\\n\",\n        \"output\": \" truck is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC[C@H](O)C(=O)N1CCC(=CC1)c2ccc(cc2F)N3C[C@H](COc4ccon4)OC3=O\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C@H1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][N][=C][Ring1][#Branch1][C][Ring1][P]\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][N][Branch2][Ring2][#Branch1][C][C][=C][N][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][Ring2][Ring1][=C]\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4r)-4-[[(2s)-2-[[(4r)-2-[(1s,2s)-1-amino-2-methylbutyl]4,5-dihydro-1,3-thiazole-4-carbonyl]amino]-4-methylpentanoyl]amino]-5-[[(2s,3s)-1-[[(3s,6r,9s,12r,15s,18r,21s)-3-(2-amino-2-oxoethyl)-18-(3-aminopropyl)-15-[(2s)-butan-2-yl]-6-(carboxymethyl)-9-(3h-imidazol-4-ylmethyl)-2,5,8,11,14,17,20-heptaoxo-12-(phenylmethyl)-1,4,7,10,13,16,19-heptazacyclopentacos-21-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-5-oxopentanoic acid\\n\",\n        \"output\": \" -0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1)C(=O)N2CCC(CC2)C(=O)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H18N4O3/c1-4-21-15(22)8-5-11-10-18-17(20-16(11)21)19-12-6-7-13(23-2)14(9-12)24-3/h5-10H,4H2,1-3H3,(H,18,19,20)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[(4-acetyl-3-hydroxy-2-propylphenoxy)methyl]-2-bromobenzoic acid\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ncnc2sccc12\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H19FN4OS/c20-12-5-3-11(4-6-12)16-8-14-17(26-16)15(18(21)25)10-23-19(14)24-13-2-1-7-22-9-13/h3-6,8,10,13,22H,1-2,7,9H2,(H2,21,25)(H,23,24)/t13-/m0/s1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=N][N][C][=Branch1][C][=O][N][Ring1][=Branch1][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=C][NH1][Ring1][Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" farmer\\n\",\n        \"output\": \" farmer is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H11N3O/c1-15-9-4-2-8(3-5-9)10-6-7-13-11(12)14-10/h2-7H,1H3,(H2,12,13,14)\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(8r)-1-azabicyclo[2.2.2]octan-8-yl]-5-phenylthiophene-2-carboxamide\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(NCC12CC3CC(CC(C3)C1)C2)c4ccccc4\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H20F6N2O3/c18-16(19,20)9-27-12-4-5-14(28-10-17(21,22)23)13(7-12)15(26)25-8-11-3-1-2-6-24-11/h4-5,7,11,24H,1-3,6,8-10H2,(H,25,26)\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-[(2,6-dichlorophenyl)amino]phenyl]acetic acid\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][C][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=N][C][=C][Ring1][#Branch1][Cl][C][=C][C][=C][N][=C][Ring2][Ring1][Branch1][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(CN1CCOCC1)c2ccccc2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch1][C][C][N][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H15Cl2N3O4S/c20-15-17-12(29-18(15)21)6-11(22-17)19(28)23-10-5-8-3-1-2-4-9(8)16(10)24-13(25)7-14(26)27/h1-4,6,10,16,22H,5,7H2,(H,23,28)(H,24,25)(H,26,27)/t10-,16-/m1/s1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1cccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)c1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" vegetarian\\n\",\n        \"output\": \" vegetarian is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[2-(1,3-benzodioxol-5-ylamino)-2-oxoethyl]piperidine-4-carboxamide\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=N][C][=N][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][=C][Ring1][P][O][C]\\n\",\n        \"output\": \" -0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5,8-difluoro-2-furan-2-yl-1,2-dihydroquinazolin-4-amine\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][NH1][C][Branch2][Ring1][Branch1][\\\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][\\\\-Ring1][O][Ring1][#Branch1][=C][Branch1][C][C][C][=Ring2][Ring1][C][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H8ClN5O/c14-7-3-4-9-8(6-7)12-17-11(10-2-1-5-20-10)18-19(12)13(15)16-9/h1-6H,(H2,15,16)\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1nn(Cc3cccc4ccccc34)c2c5ccncc5\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H16Cl2N4O3S/c1-7-10(16)11(17)12(18-7)13(22)19-8-2-4-21(5-3-8)15-20-9(6-25-15)14(23)24/h6,8,18H,2-5H2,1H3,(H,19,22)(H,23,24)\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" propan-2-yl 4-[5-methyl-6-[(2-methyl-6-methylsulfonylpyridin-3-yl)amino]pyrimidin-4-yl]oxypiperidine-1-carboxylate\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][Branch1][C][C][Branch1][Branch2][C][O][C][=Branch1][C][=O][N][C][O][C][=Branch1][C][=O][N][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[4-(3-ethyl-2-methylimidazol-4-yl)pyrimidin-2-yl]amino]-n-(2-methoxyethyl)benzenesulfonamide\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H15F2N3O3/c1-25-15-6-10-13(7-16(15)26-2)22-8-11(18(21)24)17(10)23-14-5-9(19)3-4-12(14)20/h3-8H,1-2H3,(H2,21,24)(H,22,23)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(methylsulfonylmethyl)-6-morpholin-4-yl-2-phenylpyrimidine\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-ethyl-5-phenyl-3-thiophen-2-yl-3h-1,4-benzodiazepin-2-amine\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(2,6-dimethylphenoxy)propan-2-amine\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1cccc(F)c1CS(=O)(=O)N2CCN(CC2)c3ncccc3C(F)(F)F\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-amino-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H33N3OS/c1-15-20(9-19(27-15)13-25-4-2-23-3-5-25)21(26)24-14-22-10-16-6-17(11-22)8-18(7-16)12-22/h9,16-18,23H,2-8,10-14H2,1H3,(H,24,26)\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccc(F)cc2)NC(=O)OCc3ccncc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" stove\\n\",\n        \"output\": \" stove is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" ophthalmologist\\n\",\n        \"output\": \" ophthalmologist is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)Nc1nc2ccc(cc2[nH]1)C(=O)c3ccccc3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H19N5OS2/c1-2-11(8-22)18-13-12-14(19-15(17)24-12)21-16(20-13)23-9-10-6-4-3-5-7-10/h3-7,11,22H,2,8-9H2,1H3,(H3,17,18,19,20,21)/t11-/m1/s1\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=Branch2][Ring1][Ring1][=N][C][Branch1][C][N][=C][Ring1][#Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1cc(O)c2C(=O)c3ccccc3Oc2c1\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][=Branch1][C][=O][C][=C][C][=Branch1][S][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1][C][C][=C][S][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cc(on1)c2ccc(cc2F)N3C[C@H](Cn4ccnn4)OC3=O\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch2][Ring2][=C][C][C][O][C][=N][NH1][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring1][#C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=Branch1][C][C][Ring2][Ring2][C]\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-(4-chlorophenyl)sulfonyl-3-propylurea\\n\",\n        \"output\": \" -0.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15F2N5OS2/c1-7(5-23)19-12-11-13(20-14(18)25-11)22-15(21-12)24-6-8-3-2-4-9(16)10(8)17/h2-4,7,23H,5-6H2,1H3,(H3,18,19,20,21,22)/t7-/m1/s1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" mark\\n\",\n        \"output\": \" mark is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(difluoromethyl)-1-[4,6-di(morpholin-4-yl)-1,3,5-triazin-2-yl]benzimidazole\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=N][=Ring1][=Branch2]\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc(Cl)c(c1)c2oc3cccnc3n2\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2c(ncnc2cc1OCCCN3CCCCC3)N4CCN(CC4)C(=O)Nc5ccc(OC(C)C)cc5\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1cccc2[nH]ncc12\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" size\\n\",\n        \"output\": \" size is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=CC2=NNC(=O)N2c3ccccc13\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" scale\\n\",\n        \"output\": \" scale is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[[3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl]methylsulfinyl]-1h-benzimidazole\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" makeup\\n\",\n        \"output\": \" makeup is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(2-fluorophenyl)-1-[(3s)-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl]urea\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(tert-butylamino)-3-[(4-morpholin-4-yl-1,2,5-thiadiazol-3-yl)oxy]propan-2-ol\\n\",\n        \"output\": \" -0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(Sc3ccc(cc3)S(=O)(=O)C)c(C)n2CC(=O)O\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H22ClN3O4/c23-16-5-6-17-15(7-16)9-18(24-17)21(29)25-19-8-14-3-1-2-4-20(14)26(22(19)30)10-13(11-27)12-28/h1-7,9,13,19,24,27-28H,8,10-12H2,(H,25,29)\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(OC)nc(n1)N2N=CC(=C(Cl)C2=O)Cl\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H7N3S/c9-8-11-10-7(12-8)6-4-2-1-3-5-6/h1-5H,(H2,9,11)\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3cccc(c3)C(F)(F)F\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(1-cyclopentyl-2-ethyl-4-methyl-3-oxopyrimido[5,4-e][1,2,4]triazin-7-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18F6N4O5S/c1-9(2)13(14(31)19(23,24)25)28-12(30)7-29-15(11-4-3-5-35-11)26-6-10(16(29)32)27-17(33)34-8-18(20,21)22/h3-6,9,13H,7-8H2,1-2H3,(H,27,33)(H,28,30)\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" wolf\\n\",\n        \"output\": \" wolf is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H28ClN3O/c1-16(2)27-12-4-5-18(14-27)15-28-17(3)26-23-11-8-20(13-22(23)24(28)29)19-6-9-21(25)10-7-19/h6-11,13,16,18H,4-5,12,14-15H2,1-3H3/t18-/m0/s1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3ccc(C)cc3\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H26N4O3/c1-3-26-21-18-6-5-17(14-19(18)28-24-21)27-13-10-16-8-11-25(12-9-16)20-7-4-15(2)22-23-20/h4-7,14,16H,3,8-13H2,1-2H3\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H21N3O5S/c1-23-6-7-24-8-9-25-12-4-2-11(3-5-12)14-10-13(15(18)21)16(26-14)20-17(19)22/h2-5,10H,6-9H2,1H3,(H2,18,21)(H3,19,20,22)\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[3-nitro-4-(2-phenylsulfanylethylamino)phenyl]sulfonyl-4-piperazin-1-ylbenzamide\\n\",\n        \"output\": \" -0.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@H](CO)Oc1cc(Oc2ccc(cc2)S(=O)(=O)C)cc(c1)C(=O)Nc3nccs3\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H16N2O3/c1-3-5-6-10(4-2)7(13)11-9(15)12-8(10)14/h3-6H2,1-2H3,(H2,11,12,13,14,15)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCCNc1cc(cc(c1Oc2ccccc2)S(=O)(=O)N)C(=O)O\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][C][C][C][O][C][Branch1][Ring1][C][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=Ring1][N][NH1][C][Ring2][Ring1][Ring1][=Ring1][#C]\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H22N4O2S/c19-16(23)14-10-15(25-17(14)21-18(20)24)13-6-4-12(5-7-13)11-22-8-2-1-3-9-22/h4-7,10H,1-3,8-9,11H2,(H2,19,23)(H3,20,21,24)\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H32ClN3O4S/c1-18-3-6-23(7-4-18)34(31,32)27-25(30)29-13-9-21(10-14-29)28-15-11-22(12-16-28)33-24-8-5-20(26)17-19(24)2/h3-8,17,21-22H,9-16H2,1-2H3,(H,27,30)\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@@H1][C][N][Branch1][=C][C][C][Branch1][Branch1][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][C][C][N][Ring1][=N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNC(=O)c1ccc(Nc2ncc(F)c(n2)c3cnc(C)n3C(C)C)cc1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[2-[(2,4-difluorophenyl)carbamoyl-heptylamino]ethyl]phenoxy]-2-methylpropanoic acid\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][#C][C][C][C][N][Branch2][Ring2][Ring1][C][C][C@@H1][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Branch2][=C][C][=C][Ring1][=Branch1][C][C][=C][N][Branch1][C][C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H30N2O2/c29-27(31)28(23-7-3-1-4-8-23,24-9-5-2-6-10-24)25-14-17-30(20-25)16-13-21-11-12-26-22(19-21)15-18-32-26/h1-12,19,25H,13-18,20H2,(H2,29,31)/t25-/m1/s1\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ncccc1OC[C@@H]2CCN2\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][=C][O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=N][C][C][N][Ring1][Branch1]\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H31ClN2O2/c24-21-2-1-19(28-18-3-5-25-6-4-18)10-20(21)22(27)26-14-23-11-15-7-16(12-23)9-17(8-15)13-23/h1-2,10,15-18,25H,3-9,11-14H2,(H,26,27)\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H22BrNO/c19-16-4-2-1-3-15(16)17(21)20-11-18-8-12-5-13(9-18)7-14(6-12)10-18/h1-4,12-14H,5-11H2,(H,20,21)\\n\",\n        \"output\": \" 4.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-hydroxy-1-[4-[4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14F2N8/c1-7-3-11(24-23-7)21-13-10(16)6-19-14(22-13)20-8(2)12-17-4-9(15)5-18-12/h3-6,8H,1-2H3,(H3,19,20,21,22,23,24)/t8-/m0/s1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H16N2O2/c1-2-13(8-7-11(16)15-12(13)17)9-3-5-10(14)6-4-9/h3-6H,2,7-8,14H2,1H3,(H,15,16,17)\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H24N2O/c24-20(23-19-5-1-4-18-17(19)3-2-6-22-18)13-21-10-14-7-15(11-21)9-16(8-14)12-21/h1-6,14-16H,7-13H2,(H,23,24)\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H29N3O3S2/c26-18-8-7-17(21-20(18)25-22(28)30-21)19(27)15-24-12-14-29-13-4-10-23-11-9-16-5-2-1-3-6-16/h1-3,5-8,19,23-24,26-27H,4,9-15H2,(H,25,28)/t19-/m0/s1\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H24N2O2S/c1-3-21(18-12-6-4-7-13-18)28-26(29)23-20-16-10-11-17-22(20)27-24(25(23)31(2)30)19-14-8-5-9-15-19/h4-17,21H,3H2,1-2H3,(H,28,29)/t21-,31?/m0/s1\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1[nH]ncc1S(=O)(=O)c2ccccc2\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3ccccc3Cl)c2cc1OC\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][C][Branch1][N][C][C][C][C][C][Ring1][#Branch1][N][Ring1][Branch1][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H20F3N7O3S/c1-31(35(2,33)34)19-12(4-3-7-25-19)10-26-18-15(21(22,23)24)11-27-20(30-18)28-14-5-6-16-13(8-14)9-17(32)29-16/h3-8,11H,9-10H2,1-2H3,(H,29,32)(H2,26,27,28,30)\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (5r)-2-[[(1s)-1-(2-fluorophenyl)ethyl]amino]-5-methyl-5-(trifluoromethyl)-1,3-thiazol-4-one\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H14N2O2/c1-2-14-15-9-11(16(14)5-1)10-3-4-12-13(8-10)18-7-6-17-12/h3-4,8-9H,1-2,5-7H2\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H19ClN2/c18-16-8-6-15(7-9-16)17(14-4-2-1-3-5-14)20-12-10-19-11-13-20/h1-9,17,19H,10-13H2\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" mother-in-law\\n\",\n        \"output\": \" mother-in-law is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (3s)-3-[[5-chloro-4-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]pyrimidin-2-yl]amino]-3-(4-fluorophenyl)-n-methylpropanamide\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-2-(6-methoxynaphthalen-2-yl)propanoic acid\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2,3-dihydro-1,4-benzodioxin-8-yl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[1-[[4-(5-methyl-6-oxo-3-phenyl-1h-pyrazin-2-yl)phenyl]methyl]piperidin-4-yl]-1h-benzimidazol-2-one\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" psychology\\n\",\n        \"output\": \" psychology is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20N6O3/c1-13-3-2-4-14(11-13)22-19-24-23-18(28-19)17(26)21-15-5-6-16(20-12-15)25-7-9-27-10-8-25/h2-6,11-12H,7-10H2,1H3,(H,21,26)(H,22,24)\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H19NO5S/c1-12-7-8-17-16(9-12)19(13(2)20(17)11-18(21)22)26(23,24)15-6-4-5-14(10-15)25-3/h4-10H,11H2,1-3H3,(H,21,22)\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCNCC(O)COc1ccccc1C(=O)CCc2ccccc2\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCC1(NC(=O)N(C)C1=O)c2ccccc2\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(3-methylbutoxy)aniline\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" pyridin-3-ylmethyl n-[[4-[(3-aminophenyl)carbamoyl]phenyl]methyl]carbamate\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H24ClN3O3S/c1-31-22-14-19(8-9-21(22)32-13-12-28-10-2-3-11-28)29-16-27-20-15-23(33-24(20)25(29)30)17-4-6-18(26)7-5-17/h4-9,14-16H,2-3,10-13H2,1H3\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H19Cl2N3O2/c19-15-1-2-17(16(20)11-15)22-7-9-23(10-8-22)18(24)13-25-12-14-3-5-21-6-4-14/h1-6,11H,7-10,12-13H2\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-chloro-1h-indazole\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-methyl-7-(2-methylpropyl)-2-(naphthalen-1-ylmethyl)-3-pyridin-4-ylpyrazolo[4,3-e]pyrimidine-4,6-dione\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4-methylphenyl)methyl (3s,4r)-3-fluoro-4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3ccc(cc3)C(=O)O)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][#Branch1][C][N][C][C][C][S][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-2-[(2,6-dichlorobenzoyl)amino]-3-[4-(2,6-dimethoxyphenyl)phenyl]propanoic acid\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cc(NC(=O)c4ccnc(c4)N5CCOCC5)ccc3C)c2cc1OCCN6CCCC6\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-(benzoyl)phenyl]propanoic acid\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[1-[4-(3-nitrophenyl)phenoxy]-4-[4-(pyrrolidine-1-carbonyl)phenyl]butan-2-yl]piperidine-2,6-dione\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(O[C@H]2CCCNC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=S(=O)(N1CCOCC1)c2cccc(c2)c3cn4cccnc4n3\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H18F4N6/c27-17-7-3-15(4-8-17)22-12-20(31)19-11-18(9-10-21(19)34-22)33-24-13-23(35-25(32)36-24)14-1-5-16(6-2-14)26(28,29)30/h1-13H,(H2,31,34)(H3,32,33,35,36)\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][=Branch2][C][C][=C][O][C][=C][Ring1][Branch1][C][Ring1][S][=O]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[[4-[(4-chlorophenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C34H33N3O5S/c1-23-9-7-8-12-32(23)43(40,41)36-34(39)27-14-13-25(31(21-27)42-3)19-28-22-37(2)30-16-15-26(20-29(28)30)33(38)35-18-17-24-10-5-4-6-11-24/h4-16,20-22H,17-19H2,1-3H3,(H,35,38)(H,36,39)\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][Branch1][=C][Ring2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-(2-chlorophenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[2-(4-fluorophenyl)-5-phenylpyrazolo[5,1-b]pyrimidin-7-yl]-n',n'-dimethylethane-1,2-diamine\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCC1CCCCC(=N1)N\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" c1ccc2cnccc2c1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H12N2O/c19-16(18-13-8-10-17-11-9-13)15-7-3-5-12-4-1-2-6-14(12)15/h1-11H,(H,17,18,19)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][=N][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][=N][C][Branch1][C][N][=N][Ring1][#C]\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-chloro-3-(2,4-dichlorophenyl)-[1,2,4]triazolo[4,5-a]pyridine\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[5-[5-[(2,4-dimethyl-1,3-thiazol-5-yl)sulfonylamino]-6-fluoropyridin-3-yl]-4-methyl-1,3-thiazol-2-yl]acetamide\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4sc(Cl)c(Cl)c4[nH]3\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)OC(=O)N1CCC(CC1)Oc2ncnc(Oc3ccc(cc3F)S(=O)(=O)C)c2C\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-tert-butyl-3-(2,5-difluorophenyl)-6-[(2-methyl-1,2,4-triazol-3-yl)methoxy]-[1,2,4]triazolo[3,4-f]pyridazine\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4ccncc4)C3=O\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (8r,9s,13s,14s)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-17-one\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(2-chlorophenyl)-4-methyl-5-(pyridin-2-ylmethyl)-1h-pyrazolo[5,4-d]pyridine-3,6-dione\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O[C@@H](CNCCCCCCCCCN1CCC(CC1)OC(=O)Nc2ccccc2c3ccccc3)c4ccc(O)c5NC(=O)C=Cc45\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2N(C3CCN(CCCN4C(=O)Nc5ccccc45)CC3)C(=O)Nc2c1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H13N3O2/c1-3-17-11-7-5-4-6-9(11)8-10-12(17)15-14(19)16(2)13(10)18/h4-8H,3H2,1-2H3\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][NH1][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=Ring1][O][\\\\C][=C][\\\\C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[[4-(2-dimethylaminoethoxy)phenyl]methyl]-3,4,5-trimethoxybenzamide\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [4-[4-[(2,4-dichlorophenyl)methylamino]pyrido[3,2-e]pyrimidin-2-yl]piperazin-1-yl]-[(2r)-piperidin-2-yl]methanone\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H16O3/c1-12(2)21-14-8-9-15-17(10-14)20-11-16(18(15)19)13-6-4-3-5-7-13/h3-12H,1-2H3\\n\",\n        \"output\": \" 4.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)N2CCN(CC2)C(=O)c3occc3\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-methoxy-4-methylamino-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)quinoline-2-carboxamide\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)OC2N(C(=O)c3nccnc23)c4ccc(Cl)cn4\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-carbamoyl-2-(2,3-dihydro-1h-inden-5-ylamino)-2-phenylacetamide\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][N][C][=C][N][=C][Branch1][#C][S][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][Ring1][S][=O]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H22F3N3O2/c1-16-24(18-10-5-6-11-20(18)27)25(33)32(15-23(30)17-8-3-2-4-9-17)26(34)31(16)14-19-21(28)12-7-13-22(19)29/h2-13,23H,14-15,30H2,1H3/t23-/m0/s1\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19N3O4S/c23-18-16-11-15(8-9-17(16)21-19(18)24)27(25,26)22-10-4-7-14(22)12-20-13-5-2-1-3-6-13/h1-3,5-6,8-9,11,14,20H,4,7,10,12H2,(H,21,23,24)/t14-/m0/s1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H29ClN4O4/c1-16(2)34-21-13-17(31-11-5-10-30-8-3-4-9-30)12-19-22(21)25(28-14-27-19)29-23-18(26)6-7-20-24(23)33-15-32-20/h6-7,12-14,16H,3-5,8-11,15H2,1-2H3,(H,27,28,29)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][N][=C][Branch1][Branch2][S][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccc(Nc2ncc3CN=C(c4cc(Cl)ccc4c3n2)c5c(F)cccc5F)cc1\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(NC1CCCC1)C(N(Cc2occc2)C(=O)c3ccc([nH]3)c4ccccc4)c5ccncc5\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)C(O)c3ccccc3\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][O][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch2][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][=N][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc(cc1)C2(CCCCC2)c3ccc(N)cc3\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(O)c2C(=O)C=CC(=O)c12\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(2-morpholin-4-ylethyl)-2,4,8-trioxo-6-phenyl-1h-pyrido[3,4-d]pyrimidin-7-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3-aminopropyl)-4-methyl-n-[1-[3-methyl-4-oxo-5-(phenylmethyl)-[1,2]thiazolo[5,4-d]pyrimidin-6-yl]propyl]benzamide\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccc(F)cc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][P][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=N][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 4.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-[(1r)-2-[2-[3-[2-(3-chlorophenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C29H27F3N4O6/c1-16(2)23(25(38)29(30,31)32)33-22(37)15-35-21(18-7-5-4-6-8-18)13-20-24(27(35)40)34-28(41)36(26(20)39)14-17-9-11-19(42-3)12-10-17/h4-13,16,23H,14-15H2,1-3H3,(H,33,37)(H,34,41)\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][N][=C][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C][C][C][N][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H14N4/c1-3-7-12(8-4-1)16-14-11-15(19-18-14)17-13-9-5-2-6-10-13/h1-11H,(H3,16,17,18,19)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1N(C(=O)C=C1C)c2ccccc2\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-phenylacetamide\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCSCCCNCCc1cccc(c1)C(F)(F)F)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch2][Ring2][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H19BrCl2N2O4/c1-13-4-2-5-16(25)20(13)22(30)29-19(24(32)33)12-14-8-10-15(11-9-14)28-23(31)21-17(26)6-3-7-18(21)27/h2-11,19H,12H2,1H3,(H,28,31)(H,29,30)(H,32,33)/t19-/m0/s1\\n\",\n        \"output\": \" -0.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)N1CCN(C(CC(=O)NCc2ccc3OCOc3c2)C1)c4ccnc(n4)n5ccnc5\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(9,10-dioxophenanthren-2-yl)butanamide\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H21ClF3N3O2/c1-10(26)23-12-7-13-3-2-4-14(8-12)25(13)17(27)24-11-5-6-16(19)15(9-11)18(20,21)22/h5-6,9,12-14H,2-4,7-8H2,1H3,(H,23,26)(H,24,27)\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H16ClNO4S/c1-11-3-8-16-15(9-11)18(12(2)20(16)10-17(21)22)25(23,24)14-6-4-13(19)5-7-14/h3-9H,10H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][#Branch1][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][C@H1][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][Cl][C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][Ring1][O][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][C][Ring1][=C][=O]\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@@H1][Branch1][C][C][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch2][Ring1][C][C][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][C@@H1][Ring2][Ring1][#Branch1][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H28N2O3/c1-3-26(4-2)23(28)17-9-10-18(21(27)15-17)20-16-24(11-13-25-14-12-24)29-22-8-6-5-7-19(20)22/h5-10,15-16,25,27H,3-4,11-14H2,1-2H3\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H11NS/c1-2-7-13(8-3-1)17-15-11-10-12-6-4-5-9-14(12)16-15/h1-11H\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (3s)-3-(2-chlorophenyl)-1-(2-diethylaminoethyl)-3-hydroxy-2-oxo-4-(trifluoromethyl)indole-6-carboxamide\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1r,5s)-3-[di(phenyl)methoxy]-8-methyl-8-azabicyclo[3.2.1]octane\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-propan-2-yloxycarbonyloxyethyl (6r,7r)-7-[[(2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" N[C@@H](Cc1c[nH]c2ccccc12)C(=O)O\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=N][C][=C][C][Branch2][Ring1][=N][O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=N][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][C][=C][Ring2][Ring2][Ring2][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1F)C(=O)Nc2ccc(Cl)nc2\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccc2c(c1)nc(Nc3cccc(Cl)c3)c4ccncc24\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-diethylaminoethyl 1-phenylcyclopentane-1-carboxylate\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-hydroxy-3-(2-methoxyphenyl)chromen-4-one\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C33H34N4O4S/c1-2-35-12-14-36(15-13-35)21-29(39)34-26-11-10-23(33-31(26)25-6-3-4-9-28(25)42-33)22-7-5-8-24-27(38)20-30(41-32(22)24)37-16-18-40-19-17-37/h3-11,20H,2,12-19,21H2,1H3,(H,34,39)\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OCCCN4CCOCC4\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H29ClN2O2/c1-23-11-19(25)16-2-3-18(22)17(7-16)20(26)24-12-21-8-13-4-14(9-21)6-15(5-13)10-21/h2-3,7,13-15,19,23,25H,4-6,8-12H2,1H3,(H,24,26)/t13?,14?,15?,19-,21?/m0/s1\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1,3-benzothiazol-2-yl)-2-methoxybenzamide\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCCNc1ccc(cc1)C(=O)OCCN(C)C\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H8N2O2S2/c12-15(13,9-4-2-6-14-9)11-8-3-1-5-10-7-8/h1-7,11H\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" detective\\n\",\n        \"output\": \" detective is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H16N2/c1-13-11-17(18-12-14-7-3-2-4-8-14)19-16-10-6-5-9-15(13)16/h2-11H,12H2,1H3,(H,18,19)\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=N][C][=Branch1][=N][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][Branch1][C][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2cc(CCC(=O)C)ccc2c1\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 9-methyl-3-[(2-methylimidazol-1-yl)methyl]-2,3-dihydro-1h-carbazol-4-one\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Branch1][C][C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][#Branch1][Ring1][S]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1c[nH]c(\\\\C=C\\\\2/C(=O)Nc3ccccc23)c1CCC(=O)O\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][C][Ring1][=Branch1][C][Branch1][Ring2][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-bromobenzamide\\n\",\n        \"output\": \" 4.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-propyl-[1,3]thiazolo[4,5-c]quinolin-4-amine\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H25ClN2/c1-2-3-4-8-14-24-21-13-15-25(17-18-9-6-5-7-10-18)22-16-19(23)11-12-20(21)22/h5-7,9-13,15-16H,2-4,8,14,17H2,1H3/b24-21+\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COCCNC(=O)c1cccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)c1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][S][C][=Branch2][Ring1][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)C1C(CC2CCC1N2C)OC(=O)c3ccccc3\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOc1ccc(NC(=O)CCc2c(C)nc3nc(C)nn3c2C)cc1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@][Branch1][S][C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2][Branch1][Ring1][N][N][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch2][Ring1][=Branch2][C][=Branch1][C][=O][C][N][C][=C][Branch1][#Branch1][C][=C][C][Ring1][=Branch1][=O][C][Branch1][C][F][Branch1][C][F][F][=C][Branch1][C][C][N][Ring2][Ring1][Ring2][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H21NO3S/c1-10(2)9-12-5-7-13(8-6-12)11(3)14(16)15-19(4,17)18/h5-8,10-11H,9H2,1-4H3,(H,15,16)/t11-/m1/s1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][F][C][=C][Branch2][Ring1][=N][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring1]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" ONC(=O)[C@@H](Cc1ccc2ccccc2c1)NS(=O)(=O)c3ccc4ccccc4c3\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][C][Branch2][Ring1][Ring2][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][C][=Branch1][Ring2][=N][Ring1][P][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][S][C][=Branch2][Ring1][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H17Cl2FN4O4S/c18-10-4-5-13(23-17(26)22-12-3-1-2-11(20)14(12)19)15(25)16(10)29(27,28)24-8-6-21-7-9-24/h1-5,21,25H,6-9H2,(H2,22,23,26)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H13N3O3/c1-10-6-7-14(21-9-15(19)20)13(8-10)18-16-11-4-2-3-5-12(11)17-18/h2-8H,9H2,1H3,(H,19,20)\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CCOc1cc(NS(=O)(=O)c2c(Cl)cc(cc2Cl)C(F)(F)F)ccc1Cl\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-7-methoxyquinolin-2-one\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H18ClF3N2O4S/c1-4-20(5-2)25(23,24)9-6-7-11(10(15)8-9)19-12(21)13(3,22)14(16,17)18/h6-8,22H,4-5H2,1-3H3,(H,19,21)/t13-/m1/s1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1(C)N=C(N)N=C(N)N1c2ccc(Oc3ccc(Cl)cc3)c(Cl)c2\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(carbamoylamino)-5-[4-[2-(2-methoxyethoxy)ethoxy]phenyl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n,n-diethyl-4-(piperazin-1-yl-quinolin-8-ylmethyl)benzamide\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-chloro-n-(2-methyl-3-oxo-1,2,4-thiadiazol-5-yl)benzamide\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H27N5O4S/c1-15-13-24-19(14-23-15)20(27)22-12-11-16-7-9-18(10-8-16)31(29,30)26-21(28)25-17-5-3-2-4-6-17/h7-10,13-14,17H,2-6,11-12H2,1H3,(H,22,27)(H2,25,26,28)\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" pea\\n\",\n        \"output\": \" pea is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(3-methoxyphenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1c2OC(=O)C=Cc2cc3ccoc13\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H12Cl2N2O5/c12-10(13)11(18)14-8(5-16)9(17)6-1-3-7(4-2-6)15(19)20/h1-4,8-10,16-17H,5H2,(H,14,18)/t8-,9-/m1/s1\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H26F3N3O7/c1-16(2)23(24(36)28(29,30)31)33-22(35)14-34-21(18-9-6-10-19(13-18)26(38)39)12-11-20(25(34)37)32-27(40)41-15-17-7-4-3-5-8-17/h3-13,16,23H,14-15H2,1-2H3,(H,32,40)(H,33,35)(H,38,39)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][C][N][C][C][O][C][=C][C][=C][C][=Branch2][Ring1][#Branch2][=N][C][=Branch1][Branch2][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2][N][C][C@@H1][Branch1][C][C][O][C@@H1][Branch1][C][C][C][Ring1][Branch2][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3cccnc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3,3,3-trifluoro-2-hydroxy-2-methyl-n-(4-pyridin-4-ylsulfonylphenyl)propanamide\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H10ClN3O4/c17-9-1-2-10-11(5-9)18-13-12(14(10)21)16(23)20(19-15(13)22)6-8-3-4-24-7-8/h1-5,7H,6H2,(H,18,21)(H,19,22)\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H33ClN4O/c24-20-19(3-6-26-21(20)27-13-15-1-4-25-5-2-15)22(29)28-14-23-10-16-7-17(11-23)9-18(8-16)12-23/h3,6,15-18,25H,1-2,4-5,7-14H2,(H,26,27)(H,28,29)\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-chloro-6-[4-(2-oxo-4h-3,1-benzoxazin-1-yl)piperidin-1-yl]-n-propan-2-ylpyridine-3-carboxamide\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(NC(C)(C)C)C(=O)c1cccc(Cl)c1\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H]1CN(Cc2cc(Cl)ccc2CC(=O)O)CCN1C(=O)Cc3ccc(Cl)cc3\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-furan-2-yl-6-furan-3-ylfuro[3,2-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H22N2O2/c1-2-20(17-11-5-3-6-12-17)27-25(29)22-19-15-9-10-16-21(19)26-23(24(22)28)18-13-7-4-8-14-18/h3-16,20,28H,2H2,1H3,(H,27,29)/t20-/m0/s1\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][C][=Branch1][C][=O][C][Branch1][S][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][=C][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" phenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[1-(4-methoxyphenyl)benzimidazol-5-yl]benzenesulfonamide\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCC(C)(C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@@H]12\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(ccc1Cc2cn(C)c3ccc(cc23)C(=O)NCCc4ccccc4)C(=O)NS(=O)(=O)c5ccccc5C\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H17ClN6O3/c1-22-6-8-23(9-7-22)17(26)27-16-14-13(19-4-5-20-14)15(25)24(16)12-3-2-11(18)10-21-12/h2-5,10,16H,6-9H2,1H3\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=C(C(=O)N(C[C@H](N)c2ccccc2)C(=O)N1Cc3c(F)cccc3F)c4ccc5OCOc5c4\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][Branch1][N][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=C][Ring2][Ring1][=C][Ring1][P]\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2nccc([C@H](O)[C@H]3C[C@@H]4CCN3C[C@@H]4C=C)c2c1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][=C][Ring1][Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring2]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-[[[1-[2-(6-chloro-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H26ClN7O2S/c1-14-4-3-5-16(23)20(14)28-21(32)17-13-24-22(33-17)27-18-12-19(26-15(2)25-18)30-8-6-29(7-9-30)10-11-31/h3-5,12-13,31H,6-11H2,1-2H3,(H,28,32)(H,24,25,26,27)\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (4s,6s)-4-ethylamino-6-methyl-7,7-dioxo-5,6-dihydro-4h-thieno[5,4-b]thiopyran-2-sulfonamide\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H15ClN4O2/c1-12-18-15(10-17(25)23(12)11-13-6-4-5-9-21-13)22-24(19(18)26)16-8-3-2-7-14(16)20/h2-10,22H,11H2,1H3\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H9NO3/c16-10-7-5-9(6-8-10)15-13(17)11-3-1-2-4-12(11)14(15)18/h1-8,16H\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9NO/c1-7-6-10(12)11-9-5-3-2-4-8(7)9/h2-6H,1H3,(H,11,12)\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" snail\\n\",\n        \"output\": \" snail is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-3-methyl-6-[2-(3-phenylphenyl)ethyl]pyrimidin-4-one\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2,3-dichloro-4-(2-methylidenebutanoyl)phenoxy]acetic acid\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[2-(tert-butylamino)-2-oxo-1-pyridin-4-ylethyl]-n-(furan-2-ylmethyl)-5-phenyl-1h-pyrrole-2-carboxamide\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1c(c2c(NS(=O)(=O)C)cccc2n1CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H30N2O4/c1-21(20(25)22-16-7-5-4-6-8-16)12-11-19(24)23(21)14-15-9-10-17(26-2)13-18(15)27-3/h9-10,13,16H,4-8,11-12,14H2,1-3H3,(H,22,25)\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15FN4O3/c1-10(21)18-7-12-8-20(15(22)23-12)11-2-3-14(13(16)6-11)19-5-4-17-9-19/h2-6,9,12H,7-8H2,1H3,(H,18,21)/t12-/m0/s1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(OC)c2nc(C)c3CCN(c4ccc(O)cc4)c3c2c1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][Branch2][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H13Cl2N5/c16-13-5-1-11(2-6-13)9-22(15-18-20-21-19-15)10-12-3-7-14(17)8-4-12/h1-8H,9-10H2,(H,18,19,20,21)\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" panty\\n\",\n        \"output\": \" panty is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2-oxo-6-phenyl-3-(sulfamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-(azepan-1-yl)-3-(4-methylphenyl)sulfonylurea\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3ccc(C)cc3F)c2cc1OC\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(CN2CCc3c(C2)[nH]c4ccccc34)cc1OC\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4-amino-2-ethylamino-1,3-thiazol-5-yl)-(5-chlorothiophen-2-yl)methanone\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)Nc1sc(cc1C(=O)N)c2ccc(CN3CCCCC3)cc2\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][S][C][=C][C][=C][N][=C][Branch1][Branch2][N][C][=Branch1][C][=O][O][C][NH1][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][C][C][C][=N][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][N][Ring1][=C][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H28Cl2N4O/c1-2-23-7-3-4-15(13-23)14-24-8-10-25(11-9-24)19(26)22-16-5-6-17(20)18(21)12-16/h5-6,12,15H,2-4,7-11,13-14H2,1H3,(H,22,26)/t15-/m0/s1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[[4-(3-methoxypropoxy)-3-methylpyridin-2-yl]methylsulfinyl]-1h-benzimidazole\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)[C@@H](N1CCc2sccc2C1)c3ccccc3Cl\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H18N4OS/c1-23-22(27)18-7-2-3-8-21(18)28-16-10-11-17-19(25-26-20(17)14-16)12-9-15-6-4-5-13-24-15/h2-14H,1H3,(H,23,27)(H,25,26)/b12-9+\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN[C@H]1C[C@H](C)S(=O)(=O)c2sc(cc12)S(=O)(=O)N\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[6-amino-8-[(7-chloro-1,3-benzothiazol-2-yl)sulfanyl]purin-9-yl]ethanol\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2nccc(Nc3cc(C)ccc3Cl)n2)cc1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H22N6O3S/c1-30-14-4-11-24-31(28,29)17-8-6-16(7-9-17)25-21-22-12-10-18(26-21)19-15-23-20-5-2-3-13-27(19)20/h2-3,5-10,12-13,15,24H,4,11,14H2,1H3,(H,22,25,26)\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H26ClN3OS/c22-17-6-7-21-19(16-17)25(18-4-1-2-5-20(18)27-21)9-3-8-23-10-12-24(13-11-23)14-15-26/h1-2,4-7,16,26H,3,8-15H2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" color\\n\",\n        \"output\": \" color is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfonyl-5-fluoro-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][=Branch2][N][C][=N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][Ring2][S][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" handle\\n\",\n        \"output\": \" handle is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][C][C][C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c([S+]([O-])CC)c(nc2ccccc12)c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring2][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][S+1][Branch1][C][O-1][C][C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H28N6O3S/c1-2-8-32-22-24-20(23-15-10-14(15)12-6-4-3-5-7-12)17-21(25-22)28(27-26-17)16-9-13(11-29)18(30)19(16)31/h3-7,13-16,18-19,29-31H,2,8-11H2,1H3,(H,23,24,25)/t13-,14+,15-,16-,18-,19+/m1/s1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H18N2O4S/c1-13-4-6-14(7-5-13)23(20,21)18-10-8-17(9-11-18)16(19)15-3-2-12-22-15/h2-7,12H,8-11H2,1H3\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C@@H1][C][C][C@H1][Ring1][Branch1][C][C@H1][Branch1][Ring2][C][Ring1][#Branch1][O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][Branch2][=C][C][=C][N][=C][Branch1][#Branch2][N][C][C][C][O][C][C][Ring1][=Branch1][N][=C][Ring2][Ring1][C][Ring1][=N][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" ball\\n\",\n        \"output\": \" ball is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1cccc(Cl)c1c2nnc3cccc(Cl)n23\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2,5-dimethyl-3-(8-methylsulfonylquinolin-4-yl)indol-1-yl]acetic acid\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-(4-fluorophenyl)-2-propan-2-yl-3-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]quinazolin-4-one\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H18N4O3/c1-9(18)6-4-5-7-17-12(19)10-11(14-8-15(10)2)16(3)13(17)20/h8H,4-7H2,1-3H3\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C37H49N3O3S/c1-3-40(37(41)28-30-14-16-35(17-15-30)44(2,42)43)34-20-25-38(26-21-34)27-22-36(32-12-8-5-9-13-32)33-18-23-39(24-19-33)29-31-10-6-4-7-11-31/h4-17,33-34,36H,3,18-29H2,1-2H3\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][N][C][C][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H27FN4O5S/c1-14(2)31-22(28)26-9-6-15(7-10-26)32-21-17-8-11-27(20(17)24-13-25-21)19-5-4-16(12-18(19)23)33(3,29)30/h4-5,12-15H,6-11H2,1-3H3\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C29H31N5O4/c1-36-26-18-24-25(19-27(26)38-15-5-12-34-13-16-37-17-14-34)30-20-31-28(24)32-22-8-10-23(11-9-22)33-29(35)21-6-3-2-4-7-21/h2-4,6-11,18-20H,5,12-17H2,1H3,(H,33,35)(H,30,31,32)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2,5-di(phenyl)-1,3,4-thiadiazole\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)-6-(2-dimethylaminoethoxy)-7-methoxyquinazolin-4-amine\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H]1C[C@H]2[C@@H]3CC[C@H](C(=O)C)[C@@]3(C)C[C@H](O)[C@@H]2[C@@]4(C)CCC(=O)C=C14\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-hydroxyxanthen-9-one\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-methoxy-n,n-dimethyl-2-pyridin-2-ylpyrimidin-4-amine\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(N2CCCN(C)CC2)c3NC(=CC(=O)c3c1)C(=O)Nc4ccc(cc4)N5CCOCC5\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=N][C][=Branch1][S][=N][C][Branch1][Branch2][N][C][C][C][C][Ring1][Branch1][=C][Ring1][O][Cl][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(cc1Cl)C2=CSC3=NCCN23\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2c(c1)[nH]c3c(C)nccc23\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)C(=O)Cc2ccccn2\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(1-adamantyl)-n-[2-[2-(2-hydroxyethylamino)ethylamino]quinolin-5-yl]acetamide\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H12N6S/c1-21-8-19-10(9-5-3-2-4-6-9)12(21)15-20-11-13(16)17-7-18-14(11)22-15/h2-8H,1H3,(H2,16,17,18)\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [S][=C][Branch1][#Branch2][N][C][C][C][C][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][N][=C][NH1][Ring1][Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=N][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][N][=N][C][Ring1][O][C][=C][C][=C][S][Ring1][Branch1][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-(1,3-thiazol-2-ylsulfamoyl)phenyl]-2,3-dihydro-1,4-benzodioxine-7-sulfonamide\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(c(Cl)c1)c2nnc3cccc(Cl)n23\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccccc1NC(=O)c2ccc(cc2)N3CCOCC3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(8r)-1-azabicyclo[2.2.2]octan-8-yl]-4-chlorobenzamide\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H29N3O/c1-4-24(20-13-7-5-8-14-20)30-28(32)26-22-17-11-12-18-25(22)29-27(23(26)19-31(2)3)21-15-9-6-10-16-21/h5-18,24H,4,19H2,1-3H3,(H,30,32)/t24-/m0/s1\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H14N2O2/c1-11-15(19)17-13-9-5-6-10-14(13)18(11)16(20)12-7-3-2-4-8-12/h2-11H,1H3,(H,17,19)\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 8-[5-(5-pyridin-3-ylfuran-2-yl)-1,3,4-oxadiazol-2-yl]-1-azabicyclo[2.2.2]octane\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" drain\\n\",\n        \"output\": \" drain is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2,5-dimethyl-3-[7-(trifluoromethyl)quinolin-4-yl]indol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)c2c(onc2c3ccncc3)C=C1c4ccccc4\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)13-8-19-14-7-11(17)5-6-12(14)15(13)18/h1-8,16-17H\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)NCCN2CCOCC2)C(F)(F)F\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(benzimidazol-1-yl)-1-(4-bromophenyl)ethanone\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H15N5O5/c1-20-9-5-8(14-11(12)15-9)16(3-13-5)10-7(19)6(18)4(2-17)21-10/h3-4,6-7,10,17-19H,2H2,1H3,(H2,12,14,15)/t4-,6-,7-,10-/m1/s1\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][O][F]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][Branch1][Branch1][O][N][=Ring1][Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][N][C][C@H1][Branch1][=Branch2][C][N][C][=C][N][=N][Ring1][Branch1][O][C][Ring1][O][=O]\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][C][O][C][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][#C][S][C][C][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=C]\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNS(=O)(=O)Cc1ccc2[nH]cc(CCN(C)C)c2c1\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" salt\\n\",\n        \"output\": \" salt is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-(1,1-dioxo1,3-thiazolidine-3-carbonyl)-3-methyl-1-propan-2-yl-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H27F2N7O/c1-13(2)31-14(3)26-12-19(31)20-18(24)11-27-22(29-20)28-15-6-7-16(17(23)10-15)21(32)25-8-9-30(4)5/h6-7,10-13H,8-9H2,1-5H3,(H,25,32)(H,27,28,29)\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-ethoxy-6-[2-[1-(6-methylpyridazin-3-yl)piperidin-4-yl]ethoxy]-1,2-benzoxazole\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H20ClN3O4S/c21-17-7-13-6-14(23-19(13)29-17)18(27)22-15-5-12-3-1-2-4-16(12)24(20(15)28)8-11(9-25)10-26/h1-4,6-7,11,15,23,25-26H,5,8-10H2,(H,22,27)\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring2][Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=C][C][=C][Branch1][=N][O][C][C][Branch1][C][O][C][N][Branch1][C][C][C][C][=C][Ring1][=C][=N][C][=N][Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNCCCN1c2ccccc2CCc3ccccc13\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" FC(F)Oc1ccc(cc1OCC2CC2)C(=O)Nc3c(Cl)cncc3Cl\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-n-(4-chloro-3-pyridin-2-ylphenyl)-4-methylsulfonylbenzamide\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)COc1ccc(cc1CN2CCN(CC2)S(=O)(=O)c3ccccc3)C(F)(F)F\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H15N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-5,11-12H,6-9H2\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][Branch1][N][C][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[6-[(2-cyclopentylacetyl)amino]benzimidazol-1-yl]methyl]-3-methoxy-n-phenylsulfonylbenzamide\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-diethylaminoethyl 1-cyclohexylcyclohexane-1-carboxylate\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[(2-chlorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-methoxy-n,2,6-trimethyl-n-[2-[2-[4-(1-methylpiperidin-4-yl)piperazin-1-yl]-2-oxoethoxy]ethyl]benzenesulfonamide\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" reindeer\\n\",\n        \"output\": \" reindeer is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H17ClO5S/c1-3-24(21,22)13-5-6-14(11(2)8-13)15-9-12(18)4-7-16(15)23-10-17(19)20/h4-9H,3,10H2,1-2H3,(H,19,20)\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H14N6OS2/c1-8-6-22-13(17-8)18-12(21)10-5-9(3-4-11(10)15)23-14-19-16-7-20(14)2/h3-7H,15H2,1-2H3,(H,17,18,21)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-acetyl-5-methyl-n-(1,3-thiazol-2-yl)-1,2-oxazole-4-carboxamide\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H11NO2/c1-12-10(13)7-9(11(12)14)8-5-3-2-4-6-8/h2-6,9H,7H2,1H3\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=C][C][=C][C][=N][N][Branch2][Ring1][#Branch2][C][=C][N][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][=C][Ring1][=Branch2][C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCc2cc(Cl)c(O)cc2[C@H](C1)c3ccccc3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)c2cc3ccccc3n2C\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 10-[2-(1-methylpiperidin-2-yl)ethyl]-2-methylsulfinylphenothiazine\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H25N3O4S/c1-27-18-7-5-17(6-8-18)19-16-30-22(23-19)25(21(26)20-4-2-13-29-20)10-3-9-24-11-14-28-15-12-24/h2,4-8,13,16H,3,9-12,14-15H2,1H3\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][Branch2][Ring1][Branch1][N][C][=C][C][=C][Branch1][=Branch1][N][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H26Cl3N3O4S/c24-16-2-1-3-20(14-16)34(31,32)27-23(30)29-10-6-17(7-11-29)28-12-8-18(9-13-28)33-19-4-5-21(25)22(26)15-19/h1-5,14-15,17-18H,6-13H2,(H,27,30)\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][Ring1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1][C][=Branch1][Ring2][=C][Ring1][S][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][=C][N][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][Cl][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H6BrNO/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H2,9,10)\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-(2-amino-2-oxoethoxy)-2-ethyl-1-(phenylmethyl)indol-3-yl]-2-oxoacetamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-(3-methyl-5-nitroimidazol-4-yl)sulfanyl-7h-purine\\n\",\n        \"output\": \" 0.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-phenyl-n-(1,3-thiazol-2-yl)acetamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][C][C][C][C][C][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,5-dichloro-n-[4-(3-chlorothiophen-2-yl)-1,3-thiazol-2-yl]benzenesulfonamide\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H23N3O4/c1-4-15(13-9-6-5-7-10-13)23-17-18(21(28)20(17)27)24-16-12-8-11-14(19(16)26)22(29)25(2)3/h5-12,15,23-24,26H,4H2,1-3H3/t15-/m1/s1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(COc1ccccc1)NC(C)C(O)c2ccc(O)cc2\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][S+1][Branch1][C][O-1][C][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CS(=O)(=O)n1c2ccccc2c3cc(NC(=O)CCc4ccncc4)ccc13\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C33H44N4O5/c1-22(34-2)30(38)35-28(25-18-11-6-12-19-25)32(40)37-21-13-20-26(37)31(39)36-29(33(41)42-3)27(23-14-7-4-8-15-23)24-16-9-5-10-17-24/h4-5,7-10,14-17,22,25-29,34H,6,11-13,18-21H2,1-3H3,(H,35,38)(H,36,39)/t22-,26-,28-,29-/m0/s1\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H17ClN4O/c18-13-3-1-2-12(10-13)15-11-19-17-5-4-16(21-22(15)17)20-14-6-8-23-9-7-14/h1-5,10-11,14H,6-9H2,(H,20,21)\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OCCCNc1ccc2c(NC(=O)CC3CCCCC3)c(Cl)ccc2n1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1Nc2ccccc2C(=O)C=C1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" macrame\\n\",\n        \"output\": \" macrame is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H10O2S/c19-17-15-4-2-1-3-13(15)14-6-5-11(9-16(14)18(17)20)12-7-8-21-10-12/h1-10H\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][NH1][C][=C][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=Ring1][O][\\\\C][=C][/C][C][N][Branch1][Branch1][C][\\\\-Ring1][Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3,4-dichlorophenyl)-4-[[(2s)-4-ethylmorpholin-2-yl]methyl]piperazine-1-carboxamide\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCC(COC(=O)c1cc(OC)c(OC)c(OC)c1)(N(C)C)c2ccccc2\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-chloro-2-[(3-methylthiophen-2-yl)methyl]-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H13ClN2O/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H14ClN3O/c14-10-1-2-11-9(7-10)8-12(16-11)13(18)17-5-3-15-4-6-17/h1-2,7-8,15-16H,3-6H2\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccccc1NC(=O)c2ccc(cc2)c3nccs3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-cyclopropyl-6-fluoro-8-methoxy-7-(3-methylpiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H14N2O2/c1-3-12(9-7-5-4-6-8-9)10(15)14(2)11(16)13-12/h4-8H,3H2,1-2H3,(H,13,16)\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (5s)-2-[[(1s)-1-(2-fluorophenyl)ethyl]amino]-5-methyl-5-(trifluoromethyl)-1,3-thiazol-4-one\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C@H1][Branch1][C][O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H9ClN2OS/c12-7-3-1-6(2-4-7)9-5-8(13)10(16-9)11(14)15/h1-5H,13H2,(H2,14,15)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-2-[[2-(benzoyl)phenyl]amino]-3-[4-[2-[5-methyl-2-(4-methylpiperazin-1-yl)-1,3-thiazol-4-yl]ethoxy]phenyl]propanoic acid\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H21N3O3S/c1-12-6-8-13(9-7-12)21(19,20)16-14(18)15-17-10-4-2-3-5-11-17/h6-9H,2-5,10-11H2,1H3,(H2,15,16,18)\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(Cc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1CC(=O)Nc2ccccc2N1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (8s,9s,10r,13s,14s,17r)-17-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,11-dione\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][S][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][Ring2][Ring1][C][=Ring1][=C]\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][Ring1][C][C][=C][C][=N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][O][Ring1][#Branch1][=C][Ring1][P][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" baritone\\n\",\n        \"output\": \" baritone is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-(4-chlorophenyl)-3-[3-methoxy-4-(2-pyrrolidin-1-ylethoxy)phenyl]thieno[2,3-e]pyrimidin-4-one\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(2-methylimidazol-1-yl)-2,2-di(phenyl)butanamide\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 8-chloro-6-piperazin-1-ylbenzo[b][1,5]benzoxazepine\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H10N2S/c1-7-9(12-10(11)13-7)8-5-3-2-4-6-8/h2-6H,1H3,(H2,11,12)\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(e)-2-(1,3-benzodioxol-5-yl)ethenyl]-1-benzothiophene-2-carboximidamide\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1cccc(NC(=O)c2ccc(CNC(=O)OCc3cccnc3)cc2)c1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H17ClN2O/c15-12-3-1-11(2-4-12)14(18)16-13-9-17-7-5-10(13)6-8-17/h1-4,10,13H,5-9H2,(H,16,18)/t13-/m0/s1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][S][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O]\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20F2N4O4/c1-25-17-11(10-22-19(24-17)23-13(4-6-26)5-7-27)8-16(18(25)28)29-15-3-2-12(20)9-14(15)21/h2-3,8-10,13,26-27H,4-7H2,1H3,(H,22,23,24)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][=C][Branch1][C][N][N][=C][Branch1][C][N][N][Ring1][Branch2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC12CC3CC(CC(C3)C1)C2\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-dimethylamino-n-[3-[(4-methoxybenzoyl)amino]-4-methylphenyl]benzamide\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]-n-(3-methoxypropyl)benzenesulfonamide\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][#C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(5-bromo-3-methoxypyrazin-2-yl)-5-dimethylaminonaphthalene-1-sulfonamide\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[4-(methylsulfonylmethyl)-6-morpholin-4-ylpyrimidin-2-yl]-1h-indole\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(tert-butylamino)-1-(3-chlorophenyl)propan-1-one\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1nc(CS(=O)(=O)c2ccc(Cl)cc2)cc(n1)N3CCOCC3\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[1-[6-[6-(propan-2-ylamino)indazol-1-yl]pyrazin-2-yl]pyrrol-3-yl]acetic acid\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O-1][N+1][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" kenya\\n\",\n        \"output\": \" kenya is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)CN(c1ccccc1C)S(=O)(=O)c2ccc(Cl)cc2\\n\",\n        \"output\": \" 4.03\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[5-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H15F3N2O4S/c1-15(23,16(17,18)19)14(22)20-11-7-9-13(10-8-11)26(24,25)21-12-5-3-2-4-6-12/h2-10,21,23H,1H3,(H,20,22)\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1CN(CCN1)C(=O)c2cc3ccccc3[nH]2\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n'-[2-amino-6-(3-chlorophenyl)pyrimidin-4-yl]-2-(4-fluorophenyl)quinoline-4,6-diamine\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" knife\\n\",\n        \"output\": \" knife is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1)C(=O)c2ccc(CC(=O)O)n2C\\n\",\n        \"output\": \" -1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccccc1[N+](=O)[O-]\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(6-chloropyridin-3-yl)-3,4-difluorobenzamide\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)N1CCN([C@H](CN2CCCC2)C1)C(=O)Cc3ccc(Cl)c(Cl)c3\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5e)-5-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H32ClN3O3/c27-23-10-9-20(16-22(23)25(31)29-17-18-6-3-1-2-4-7-18)21-8-5-13-28-24(21)30-14-11-19(12-15-30)26(32)33/h5,8-10,13,16,18-19H,1-4,6-7,11-12,14-15,17H2,(H,29,31)(H,32,33)\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (8r,9s,10r,13s,14s)-10,13-dimethyl-6-methylidene-7,8,9,11,12,14,15,16-octahydrocyclopenta[a]phenanthrene-3,17-dione\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H11NO/c1-7-5-3-4-6-9(7)10-8(2)11/h3-6H,1-2H3,(H,10,11)\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ncccc1NCc2cccc(c2)c3cccnc3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" captain\\n\",\n        \"output\": \" captain is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H14N2/c1-12-7-3-5-10(12)9-4-2-6-11-8-9/h2,4,6,8,10H,3,5,7H2,1H3\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" factory\\n\",\n        \"output\": \" factory is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)Nc1ccc(NCc2ccc(F)cc2)nc1N\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H34N4O2/c30-9-8-26-6-7-27-23-5-4-20-21(28-23)2-1-3-22(20)29-24(31)16-25-13-17-10-18(14-25)12-19(11-17)15-25/h1-5,17-19,26,30H,6-16H2,(H,27,28)(H,29,31)\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 8-fluoro-5-methyl-6-oxo-4h-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10,13H\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[6-amino-8-[(7-chloro-1,3-benzothiazol-2-yl)sulfanyl]purin-9-yl]ethyl acetate\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-bromo-2-(4-methoxyphenyl)-6,7-dihydro-5h-pyrrolo[1,2-a]imidazole\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(9-propan-2-ylcarbazol-3-yl)morpholine-4-carboxamide\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H24FN3O5S/c18-15-1-3-16(4-2-15)19-7-9-20(10-8-19)27(24,25)13-17(21(23)14-22)5-11-26-12-6-17/h1-4,14,23H,5-13H2\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(COC(=O)N2CCC(CNc3ncccn3)CC2)cc1\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(CNC(=O)CCS(=O)(=O)c2ccc(Br)cc2)cc1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H23Cl2N3O3S/c1-26-20-10-3-6-14(27-20)5-2-7-15-11-12-16(32-15)13-19(23(30)31)28-22(29)21-17(24)8-4-9-18(21)25/h3-4,6,8-12,19H,2,5,7,13H2,1H3,(H,26,27)(H,28,29)(H,30,31)/t19-/m0/s1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OCCN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch2][Ring1][C][\\\\C][=C][\\\\C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][Branch1][O][O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring1][=C][C]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(Oc1c(Cl)cccc1Cl)C2=NCCN2\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(4-chlorophenyl)-1,3-thiazol-2-amine\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[(4,8-dimethyl-[1,2,4]triazolo[4,5-a]quinolin-1-yl)sulfanyl]-1-[4-(furan-2-carbonyl)piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H8ClN5/c10-6-3-1-5(2-4-6)7-13-8(11)15-9(12)14-7/h1-4H,(H4,11,12,13,14,15)\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][=N][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Ring1][O][N][Ring1][=C][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H17N5O3/c1-22-7-8-23-14-18-12(16)11-13(19-14)20(15(21)17-11)9-10-5-3-2-4-6-10/h2-6H,7-9H2,1H3,(H,17,21)(H2,16,18,19)\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H23NO/c1-15-9-7-8-12-17(15)18(20-14-13-19(2)3)16-10-5-4-6-11-16/h4-12,18H,13-14H2,1-3H3\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" gemini\\n\",\n        \"output\": \" gemini is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C1CN=C(N1)c2ccc3ccccc3n2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[[4-[[4-(2,4-difluorophenyl)piperazin-1-yl]methyl]phenyl]methyl]acetamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc2nc3ccccc3c(N)c2c1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[3-[4-[3-(4-fluorophenyl)-1,2-oxazol-5-yl]phenoxy]propyl]-4-methylpiperazine\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COCCOc1nc(N)c2NC(=O)N(Cc3ccccc3)c2n1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C]\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H14N4O4S/c1-19-10-11(14-7-15-12(10)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16)\\n\",\n        \"output\": \" -0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H28ClN3O3S2/c23-17-5-2-1-4-15(17)8-10-24-11-13-30-12-3-9-25-14-19(28)16-6-7-18(27)20-21(16)31-22(29)26-20/h1-2,4-7,19,24-25,27-28H,3,8-14H2,(H,26,29)/t19-/m0/s1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cc(CCCOc2c(Cl)cc(cc2Cl)C3=NCCO3)on1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H29F3N4O5/c1-16(2)24(25(37)28(29,30)31)34-23(36)14-35-22(20-8-6-5-7-9-20)11-10-21(26(35)38)33-27(39)40-15-19-12-17(3)32-18(4)13-19/h5-13,16,24H,14-15H2,1-4H3,(H,33,39)(H,34,36)\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(3-chloro-4-fluorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CSc1ccc2Sc3ccccc3N(CCC4CCCCN4C)c2c1\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)C2=CC(=O)c3cc(O)ccc3O2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][Branch2][Ring2][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][#Branch2][C][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][Branch1][=Branch2][C][Branch1][C][F][Branch1][C][F][F][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-6-(1h-indol-3-ylmethyl)-3-methyl-1-(2-methylpropyl)thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-10-[3-(4-methylpiperazin-1-yl)propyl]phenothiazine\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][N][Branch1][O][C][O][P][=Branch1][C][=O][Branch1][C][O][O][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H13N3O3S/c1-10(17)15-11-5-7-12(8-6-11)20(18,19)16-13-4-2-3-9-14-13/h2-9H,1H3,(H,14,16)(H,15,17)\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" FC(F)(F)c1cc(NC(=O)c2cnc(Cl)nc2C(F)(F)F)cc(c1)C(F)(F)F\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][Branch2][Ring1][N][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][N][Branch1][C][C][S][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccccc1OCC(=O)NC2CCCC2\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-pyridin-3-ylpyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H15N3O/c1-16-12(17)9-11(15-13(16)14)8-7-10-5-3-2-4-6-10/h2-6,9H,7-8H2,1H3,(H2,14,15)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-cyclohexyl-4-(3h-imidazol-4-yl)piperidine-1-carbothioamide\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" bagel\\n\",\n        \"output\": \" bagel is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1s,9s)-n-[(2r,3s)-2-ethoxy-5-oxooxolan-3-yl]-9-(isoquinoline-1-carbonylamino)-6,10-dioxo-2,3,4,7,8,9-hexahydro-1h-pyridazino[1,2-a]diazepine-1-carboxamide\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Branch1][Ring1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][Branch1][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(N3CC[C@H](C3)Oc4cnc5ccccc5n4)c2cc1OC\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1=CC2=NNC(=O)N2c3cc(ccc13)c4ccncc4\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-butylamino-4-(phenoxy)-5-sulfamoylbenzoic acid\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1sc2ncnc(SCC(=O)N3CCCC3)c2c1C\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-n-[1-[2-(hydroxyamino)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][C][C][C@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H22O7/c1-11-5-3-7-14(20)18(23)15(21)8-4-6-12-9-13(25-2)10-16(22)17(12)19(24)26-11/h3-4,6-7,9-11,15,18,21-23H,5,8H2,1-2H3/b6-4+,7-3-/t11-,15-,18+/m0/s1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cnc(nc1Oc2ccc(F)cc2F)c3ccccn3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CCCN1c2ccccc2Sc3ccc(cc13)C(F)(F)F\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H7BO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5,10-11H\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-phenylsulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1C(C(=O)Nc2ncc(C)s2)C(=O)c3ccccc3S1(=O)=O\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-dimethylaminoethyl 4-butylaminobenzoate\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(CSc1ccccc1)N2CCN(CC2)C(=O)c3occc3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 8-hydroxyquinoline-2-carboxylic acid\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-[(6-fluoroquinolin-4-yl)methyl]-5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[4,5-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Ring1][#Branch1][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][S][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C@H1][C][C][C][N][C@H1][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H17ClN2O5S/c1-11-18(26-13-8-6-12(19)7-9-13)17-14(20-27(2,24)25)4-3-5-15(17)21(11)10-16(22)23/h3-9,20H,10H2,1-2H3,(H,22,23)\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][C][Ring1][Branch1][C][C][O][C][Branch1][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)(C)C(=O)Nc1ccc2c(c1)C(=O)C(=O)c3ccccc23\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2,3-dihydroxypropyl 2-[(7-chloroquinolin-4-yl)amino]benzoate\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[2-(4-hydroxyphenyl)ethyl]phenol\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" patio\\n\",\n        \"output\": \" patio is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-[[[1-[2-(3-fluoro-6-methoxy-1,5-naphthyridin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H35N7O2/c1-4-19-7-6-8-20(5-2)25(19)29-28(37)35-17-23-24(18-35)31-32-26(23)30-27(36)21-9-11-22(12-10-21)34-15-13-33(3)14-16-34/h6-12H,4-5,13-18H2,1-3H3,(H,29,37)(H2,30,31,32,36)\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][=Branch2][C][C][=C][C][=C][S][Ring1][Branch1][C][Ring1][S][=O]\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-(4-methylpiperazin-1-yl)quinazolin-4-yl]-n'-(4-nitrophenyl)ethane-1,2-diamine\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][N][=C][C][=C][C][=C][Branch1][C][Cl][N][Ring1][#Branch2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1)C(=O)C2CCN(CCN3C(=O)Nc4ccccc4C3=O)CC2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cnc(Nc2ccc(OCCN3CCCC3)cc2)nc1Nc4cccc(c4)S(=O)(=O)NC(C)(C)C\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(Nc2ccc(F)cc2)nc(N)n1\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[6-chloro-5-[(2r,5s)-4-[(4-fluorophenyl)methyl]-2,5-dimethylpiperazine-1-carbonyl]-1-methylindol-3-yl]-n,n-dimethyl-2-oxoacetamide\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H22FN3O6/c1-3-4-5-6-24-15(23)18-12-9(16)7-19(14(22)17-12)13-11(21)10(20)8(2)25-13/h7-8,10-11,13,20-21H,3-6H2,1-2H3,(H,17,18,22,23)/t8-,10-,11-,13-/m1/s1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=N][C][=N][C][=Branch2][Ring1][Branch1][=C][C][Branch1][N][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1][=C][Ring1][P][Ring1][=N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H21N/c1-10(2)8-5-6-9(7-8)11(10,3)12-4/h8-9,12H,5-7H2,1-4H3\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H20FNO3/c1-25-18-8-4-14(5-9-18)19(23)15-10-12-22(13-11-15)20(24)16-2-6-17(21)7-3-16/h2-9,15H,10-13H2,1H3\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1C(=N)N(CC(=O)c2ccc(Cl)cc2)c3ccccc13\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [5-chloro-2-[2-[(2r)-4-[(4-fluorophenyl)methyl]-2-methylpiperazin-1-yl]-2-oxoethoxy]phenyl]urea\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring2][Branch2][N][Branch2][Ring1][=Branch2][C][Branch1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC12CC3CC(C)(C1)CC(N)(C3)C2\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H23N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h11-13H,1-10H2\\n\",\n        \"output\": \" -0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1)C2=COc3cc(OC)cc(OC)c3C2=O\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COC(=O)COc1ccc(OCCNCC(O)COc2ccccc2)cc1\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H16N2O5S2/c1-10-4-5-11(16(20)24-3)8-14(10)18-26(22,23)12-6-7-15-13(9-12)17(21)25-19(15)2/h4-9,18H,1-3H3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H36O7/c1-4-13(2)23(29)30-20-11-17(25)9-15-6-5-14(3)19(22(15)20)8-7-16(24)10-18(26)12-21(27)28/h5-6,9,13-14,16-20,22,24-26H,4,7-8,10-12H2,1-3H3,(H,27,28)/t13-,14-,16+,17+,18+,19-,20-,22-/m0/s1\\n\",\n        \"output\": \" -0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H14O3/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10/h3-9H,1-2H3,(H,15,16)\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][Branch1][C][Branch2][Ring1][P][N][Branch1][=Branch2][C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1h-indazol-4-yl)thiophene-2-sulfonamide\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10FN3S/c13-7-3-1-4-8-10(7)11(14)16-12(15-8)9-5-2-6-17-9/h1-6,12,15H,(H2,14,16)\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-oxo-6-phenyl-3-(phenylmethylsulfamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][Branch1][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][Branch1][N][C][C][C][C][C][Ring1][Branch1][C][=C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(c1ccnc(Nc2cccc(c2)S(=O)(=O)C)n1)c3cccc4[nH]ncc34\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H14Cl2N4O3/c19-14-4-2-1-3-11(14)7-8-21-17(26)13-9-12(5-6-15(13)20)24-18(27)23-16(25)10-22-24/h1-6,9-10H,7-8H2,(H,21,26)(H,23,25,27)\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H17NO3/c15-11-7-3-4-8-12(11)17-9-13(16)14-10-5-1-2-6-10/h3-4,7-8,10,15H,1-2,5-6,9H2,(H,14,16)\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1)C(CN(C)C)C2(O)CCCCC2\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H11NO/c1-3-10(12)11-9-6-4-8(2)5-7-9/h3-7H,1H2,2H3,(H,11,12)\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H23N5O2S/c1-3-14-21-15-16(12-8-4-5-9-13(12)20-17(15)18)22(14)11-7-6-10-19-25(2,23)24/h4-5,8-9,19H,3,6-7,10-11H2,1-2H3,(H2,18,20)\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCCC(O)c1[nH]c2cc(C)c(cc2c1CCc3ccccc3)C(=O)O\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCC1=CC(=O)NC(=S)N1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2c(c1)cc(C(=O)O)n2Cc3ccc(Cl)c(Cl)c3\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][N][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][C][S][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=N)c1cc2c(cccc2s1)c3ccccc3\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-bromo-4-(4-chlorobenzoyl)-n-methyl-1h-pyrrole-2-carboxamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CCOc2n[nH]c3ncnc(Nc4ccc(OCc5ccccn5)c(Cl)c4)c23)CC1\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (5z)-5-[(2,2-difluoro-1,3-benzodioxol-5-yl)methylidene]-1,3-thiazolidine-2,4-dione\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-morpholin-4-ylethyl (e)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-4-methylhex-4-enoate\\n2-morpholin-4-ylethyl 6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1h-2-benzofuran-5-yl)-4-methylhex-4-enoate\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H27F3N4O5S/c1-17(2)23(24(35)26(27,28)29)31-22(34)16-33-21(19-11-7-4-8-12-19)14-13-20(25(33)36)32-39(37,38)30-15-18-9-5-3-6-10-18/h3-14,17,23,30,32H,15-16H2,1-2H3,(H,31,34)\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H11N5O/c1-7(16)12-10-13-9(11)15(14-10)8-5-3-2-4-6-8/h2-6H,1H3,(H3,11,12,13,14,16)\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(2,4-dichlorophenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H15N3O2S2/c1-21-12-6-4-11(5-7-12)9-18-14(20)10-22-16-19-13-3-2-8-17-15(13)23-16/h2-8H,9-10H2,1H3,(H,18,20)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)N1CCC(CC1)N(C(=O)Cc2ccccc2)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20F2N6O/c1-10(2)27-11(3)23-9-16(27)17-15(21)8-24-19(26-17)25-12-5-6-13(14(20)7-12)18(28)22-4/h5-10H,1-4H3,(H,22,28)(H,24,25,26)\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(2,4-dihydroxyphenyl)-2-phenylethanone\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=N][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3,4-dichlorophenyl)-4-[[(3r)-1-ethylpiperidin-3-yl]methyl]piperazine-1-carboxamide\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)C[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4sc(Cl)c(Cl)c4[nH]3\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][N][C][C][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl]-2-methyl-6,7,8,9-tetrahydropyrido[2,1-b]pyrimidin-4-one\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[4-(4-phenylphthalazin-1-yl)piperazin-1-yl]butan-1-one\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-phenylpteridine-2,4,7-triamine\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [4-(4-fluorobenzoyl)piperidin-1-yl]-morpholin-4-ylmethanone\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-ethyl-2-methyl-5-(morpholin-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H26Cl2N4O2/c1-2-23-7-3-4-14(13-23)18(26)24-8-10-25(11-9-24)19(27)22-15-5-6-16(20)17(21)12-15/h5-6,12,14H,2-4,7-11,13H2,1H3,(H,22,27)/t14-/m1/s1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[[5-bromo-2-[(4-chlorophenyl)methoxy]phenyl]methylamino]ethanol\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" stream\\n\",\n        \"output\": \" stream is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ncnc2c1nc(Sc3nc4cccc(Cl)c4s3)n2CCO\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(OC2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-[[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-yl]amino]phenyl]benzamide\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C28H37N7O3/c1-20-6-7-22(31-26(36)21-8-10-29-25(16-21)35-12-14-37-15-13-35)17-23(20)32-24-9-11-30-27(33-24)38-19-28(2,3)18-34(4)5/h6-11,16-17H,12-15,18-19H2,1-5H3,(H,31,36)(H,30,32,33)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H28N2O5/c1-23(2)10-11-28-17-8-6-15(7-9-17)14-22-21(24)16-12-18(25-3)20(27-5)19(13-16)26-4/h6-9,12-13H,10-11,14H2,1-5H3,(H,22,24)\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccc(O)cc2)C(F)(F)F\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-amino-n-(2-diethylaminoethyl)benzamide\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[5-[[7-[3-(ethyl-(2-hydroxyethyl)amino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]-n-(3-fluorophenyl)acetamide\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16ClNOS/c1-12-2-4-13(5-3-12)11-19-15-10-14(18)6-7-16(15)21-9-8-17(19)20/h2-7,10H,8-9,11H2,1H3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)c1ccccc1Nc2cccc(c2)C(F)(F)F\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CSCc1cc(nc(n1)c2ccccc2)N3CCOCC3\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)S(=O)(=O)Nc2nc(cs2)c3sccc3Cl\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(O)c(O)c1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC(=O)c1cccc(c1c2ccc(CC(C)C)cc2)S(=O)(=O)Nc3ncc(C)nc3OC\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H24N2/c1-20(2)14-7-15-21-18-10-5-3-8-16(18)12-13-17-9-4-6-11-19(17)21/h3-6,8-11H,7,12-15H2,1-2H3\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21N/c1-2-4-15(5-3-1)16-6-8-17(9-7-16)19-14-20-12-10-18(19)11-13-20/h1-9,18-19H,10-14H2\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3ccccc3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccc2ccccc2n1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H23F4N5O5/c1-14(2)20(21(36)25(27,28)29)33-19(35)12-34-22(16-3-5-17(26)6-4-16)31-11-18(23(34)37)32-24(38)39-13-15-7-9-30-10-8-15/h3-11,14,20H,12-13H2,1-2H3,(H,32,38)(H,33,35)\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(carbamoylamino)-5-thiophen-3-ylthiophene-2-carboxamide\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)C)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OB(O)c1ccccc1C=O\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H26N4O4/c1-13(2)26-20(25)24-10-7-16(8-11-24)27-18-14(3)19(23-12-22-18)28-17-6-5-9-21-15(17)4/h5-6,9,12-13,16H,7-8,10-11H2,1-4H3\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][=Branch2][C][C][=Branch1][C][=O][N][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H17ClN2O6S2/c1-11-18(29(26,27)13-8-6-12(19)7-9-13)17-14(20-28(2,24)25)4-3-5-15(17)21(11)10-16(22)23/h3-9,20H,10H2,1-2H3,(H,22,23)\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2nccc(Nc3ccc(Cl)cc3)n2)cc1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(5-chloro-3-methoxypyrazin-2-yl)-5-dimethylaminonaphthalene-1-sulfonamide\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C@@H1][Branch1][S][S][C][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][C][Ring1][#Branch1][C][=C][C][=C][C][Branch2][Ring1][Ring2][\\\\C][=C][\\\\C][=C][C][=C][C][=C][C][Branch1][C][Cl][=C][C][Ring1][#Branch1][=N][Ring1][O][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" [O-][N+](=O)c1cc(ccc1NCCSc2ccccc2)S(=O)(=O)NC(=O)c3ccc(cc3)N4CCNCC4\\n\",\n        \"output\": \" -0.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch2][Ring2][#C][N][C][=Branch1][C][=O][C][C][C][C][N][Branch2][Ring1][=N][C][C][C][=C][N][Branch1][Ring2][C][=Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][C][Ring2][Ring1][=Branch1][C][=C][N][C][=Branch1][C][=O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][\\\\C][=Branch2][Ring1][=N][=C][Branch1][=Branch2][/C][=C][C][=C][C][=C][Ring1][=Branch1][\\\\C][=C][C][=C][Branch1][Branch2][\\\\C][=C][\\\\C][=Branch1][C][=O][O][C][=C][Ring1][O][\\\\C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" beret\\n\",\n        \"output\": \" beret is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H27Cl2N7O/c25-17-7-6-16(19(26)14-17)15-29-22-18-4-3-9-28-21(18)30-24(31-22)33-12-10-32(11-13-33)23(34)20-5-1-2-8-27-20/h3-4,6-7,9,14,20,27H,1-2,5,8,10-13,15H2,(H,28,29,30,31)/t20-/m1/s1\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H18F2N2OS/c20-15-3-1-13(2-4-15)18(24)14-9-11-23(12-10-14)19(25)22-17-7-5-16(21)6-8-17/h1-8,14H,9-12H2,(H,22,25)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-[(4-methoxyphenyl)methyl]-3-methyl-1-(2-methylpropyl)pyrrolo[3,4-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H18ClFN6O/c19-13-8-21-18(22-15(9-27)11-3-5-12(20)6-4-11)24-17(13)23-16-7-14(25-26-16)10-1-2-10/h3-8,10,15,27H,1-2,9H2,(H3,21,22,23,24,25,26)/t15-/m0/s1\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCCC(CC)CNC(=O)c1cc(ccc1Cl)N2N=CC(=O)NC2=O\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][#Branch1][C][N][C][C][O][C][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H29NO/c23-21(19-7-3-1-4-8-19,11-14-22-12-5-2-6-13-22)20-16-17-9-10-18(20)15-17/h1,3-4,7-10,17-18,20,23H,2,5-6,11-16H2\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H15NO/c15-13-6-8-14(9-7-13)16-11-10-12-4-2-1-3-5-12/h1-9H,10-11,15H2\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H13NO3/c1-18-11-8-6-10(7-9-11)15-13-5-3-2-4-12(13)14(16)17/h2-9,15H,1H3,(H,16,17)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c([S+](C)[O-])c(nc2ccccc12)c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccc(cc1)S(=O)(=O)N2CCCC2\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C@H1][Branch1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H19ClN2O/c18-14-8-9-15-13(7-4-10-19-15)16(14)17(21)20-11-12-5-2-1-3-6-12/h4,7-10,12H,1-3,5-6,11H2,(H,20,21)\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCC(CO)NCCNC(CC)CO\\n\",\n        \"output\": \" -1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H39N7O3/c1-5-22-27(37)34(3)23-17-29-28(32-25(23)35(22)20-8-6-7-9-20)31-21-11-10-18(16-24(21)38-4)26(36)30-19-12-14-33(2)15-13-19/h10-11,16-17,19-20,22H,5-9,12-15H2,1-4H3,(H,30,36)(H,29,31,32)/t22-/m1/s1\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)c2cc3cc(C)ccc3[nH]2\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N]\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H28FN5O3/c1-31-23-3-2-20-24(29-23)18(19(25)14-28-20)6-9-30-7-4-16(5-8-30)26-13-17-12-21-22(15-27-17)33-11-10-32-21/h2-3,12,14-16,26H,4-11,13H2,1H3\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc2nc(sc2c1)c3ccccc3\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H15N3O2/c1-22-16-5-3-2-4-13(16)11-19-17(21)15-7-6-12-10-18-9-8-14(12)20-15/h2-10H,11H2,1H3,(H,19,21)\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][C][N][Branch2][Ring2][#Branch1][C][C][=C][N][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][Ring2][Ring1][=C]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(c(F)c2)n3ccnc3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(4-chlorophenyl)methyl]-2-(1-methylazepan-4-yl)phthalazin-1-one\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H23N7O2S/c1-27(2)14-12-24-31(29,30)17-8-6-16(7-9-17)25-21-22-11-10-18(26-21)19-15-23-20-5-3-4-13-28(19)20/h3-11,13,15,24H,12,14H2,1-2H3,(H,22,25,26)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H15NO3/c1-10-3-5-11(6-4-10)15(19)13-8-7-12(16(13)2)9-14(17)18/h3-8H,9H2,1-2H3,(H,17,18)\\n\",\n        \"output\": \" -1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCS(=O)(=O)Nc1cccc2c1c(Oc3ccc(Cl)cc3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" -0.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H21N3O2/c1-14(2)24-19-13-23(12-18(19)20(25)22(3)21(24)26)11-16-9-6-8-15-7-4-5-10-17(15)16/h4-10,12-14H,11H2,1-3H3\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H16O2/c1-11(16)3-4-12-5-6-14-10-15(17-2)8-7-13(14)9-12/h5-10H,3-4H2,1-2H3\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-fluorophenyl)-5,7-dihydroxychromen-4-one\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3cccc(Cl)c3Cl)c2cc1OC\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)CCNC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H15ClF2N4O2/c26-15-6-9-17-18(10-15)23(21-19(27)2-1-3-20(21)28)29-11-14-12-30-25(32-22(14)17)31-16-7-4-13(5-8-16)24(33)34/h1-10,12H,11H2,(H,33,34)(H,30,31,32)\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (3,4-dihydroxy-5-nitrophenyl)-(4-methylphenyl)methanone\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-dimethylaminoethyl)-2-fluoro-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][Ring1][N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][N][C][C][C][NH1][C][=Branch1][#Branch1][=C][C][Ring1][=Branch2][=Ring1][Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1CCC(CC(=O)Nc2cccc3ncccc23)CC1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-methyl-4-morpholin-4-yl-6-(phenylsulfonylmethyl)pyrimidine\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [1-(4-fluorobenzoyl)piperidin-4-yl]-(4-fluorophenyl)methanone\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [(1s,3r,7s,8s,8ar)-8-[2-[(2r,4r)-4-hydroxy-6-oxooxan-2-yl]ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2,2-dimethylbutanoate\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][C][F][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][#C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][=C][Ring1][S][C]\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-aminophenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=N][C][Branch1][#Branch2][S][C][C][=C][C][=C][S][Ring1][Branch1][=N][NH1][Ring1][N]\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][=C][N][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][C][Branch1][C][F][=C][Ring1][S]\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Oc2ccc(Cl)cc2)c3cc(ccc3n1CC(=O)O)C(F)(F)F\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(1-hydroxypentyl)-6-methyl-3-(2-phenylethyl)-1h-indole-5-carboxylic acid\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H30N2O2/c1-4-26(5-2)24(27)20-12-10-18(11-13-20)23(19-14-16-25-17-15-19)21-8-6-7-9-22(21)28-3/h6-13,25H,4-5,14-17H2,1-3H3\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][C][=C][Branch1][O][S][C][=Ring1][Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C@H1][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@@H1][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][\\\\C][=C][\\\\S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C][Branch2][Ring1][O][C][C][N][C][C][C][Branch1][C][O][Branch1][Branch1][C][C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCc1ncc(\\\\C=C(/Cc2cccs2)\\\\C(=O)O)n1Cc3ccc(cc3)C(=O)O\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-ethyl-6,8-difluoro-7-(3-methylpiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[3-(trifluoromethyl)phenyl]-1,3,5-triazine-2,4-diamine\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(4-methylphenyl)methyl]-2-methylsulfanylpyridine-3-carboxamide\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC[C@H](O)CN1C(=O)C=NN(C1=O)c2ccc(Cl)c(c2)C(=O)NCC3(O)CCCCCC3\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1sc(CN2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN([C@H]1CC[C@@]2(CCCO2)C[C@@H]1N3CCCC3)C(=O)Cc4ccccc4\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-2-[3-(benzoyl)phenyl]propanoic acid\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][=Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][Branch2][Ring2][P][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][S][=O][C][=C][Ring2][Ring2][Branch2]\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H14N2O2S/c1-3-11(15)14-12-13-9-6-5-8(16-4-2)7-10(9)17-12/h5-7H,3-4H2,1-2H3,(H,13,14,15)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)Nc2ccccc2)C(F)(F)F\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H9F3N2O2/c14-13(15,16)8-3-1-4-9(7-8)18-11-10(12(19)20)5-2-6-17-11/h1-7H,(H,17,18)(H,19,20)\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" example\\n\",\n        \"output\": \" example is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" lamb\\n\",\n        \"output\": \" lamb is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H]1CN(CC2(CC2)C(=O)N)CCN1S(=O)(=O)c3ccc(cc3)C(C)(O)C(F)(F)F\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-(4-pentylphenyl)-1,3,4-thiadiazol-2-amine\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(NC(=O)c2ccnc(c2)N3CCOCC3)cc1Nc4ccnc(Cl)n4\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CSc1ncccc1C(=O)NCc2ccc(C)cc2\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(1-ethylpyrrolidin-2-yl)methyl]-2-methoxy-5-sulfamoylbenzamide\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H27NO3/c1-3-4-10-21(25)22-17(12-11-16-8-6-5-7-9-16)19-14-18(23(26)27)15(2)13-20(19)24-22/h5-9,13-14,21,24-25H,3-4,10-12H2,1-2H3,(H,26,27)\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H26N2O4S/c1-15(25)28-20-21(16-9-11-17(27-4)12-10-16)29-19-8-6-5-7-18(19)24(22(20)26)14-13-23(2)3/h5-12,20-21H,13-14H2,1-4H3/t20-,21+/m1/s1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][N][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring1][#C][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoic acid\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)C[S+]([O-])C(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#C][N][=C][N][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc2ccc(cc2[nH]1)C(=O)c3ccccc3\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C@H1][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H26ClFN4O2/c1-30-21-14-20-17(13-22(21)31-11-5-10-29-8-3-2-4-9-29)23(27-15-26-20)28-16-6-7-19(25)18(24)12-16/h6-7,12-15H,2-5,8-11H2,1H3,(H,26,27,28)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" test\\n\",\n        \"output\": \" test is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)c2cn3ccccc3n2\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H27N3O3/c1-19-25(26(30(29-19)14-15-31)21-9-4-3-5-10-21)17-20-8-6-11-22(16-20)27(32)28-23-12-7-13-24(18-23)33-2/h3-13,16,18,31H,14-15,17H2,1-2H3,(H,28,32)\\n\",\n        \"output\": \" 4.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(3-amino-2-methylphenyl)methyl]-4-(2-thiophen-2-ylethoxy)pyridin-2-one\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H17FN2O5/c19-16-9-13(1-2-15(16)12-3-6-23-7-4-12)21-10-14(26-18(21)22)11-24-17-5-8-25-20-17/h1-3,5,8-9,14H,4,6-7,10-11H2/t14-/m1/s1\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C][C@@H1][Branch2][Ring2][Branch2][C@H1][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring1][Ring2][O][C][C][=C][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][N][O]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][C][C][C][C@@H1][Ring1][Branch1][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN[C@@H](C)C(=O)N[C@@H](C1CCCCC1)C(=O)N2CC[C@H]3CCN(CCc4ccccc4)C[C@@H]23\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H17BrN4O3S/c1-22(2)13-8-4-7-12-11(13)6-5-9-14(12)26(23,24)21-16-17(25-3)20-15(18)10-19-16/h4-10H,1-3H3,(H,19,21)\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [(3s)-3-dimethylaminopyrrolidin-1-yl]-[4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]methanone\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][#Branch2][O][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H18N2O3/c1-15-2-4-18(5-3-15)25-19-8-6-17(7-9-19)24-14-20(23)22-16-10-12-21-13-11-16/h2-13H,14H2,1H3,(H,21,22,23)\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H21N3O3S/c1-13-16(19-9-8-17(13)24-11-5-10-23-2)12-25(22)18-20-14-6-3-4-7-15(14)21-18/h3-4,6-9H,5,10-12H2,1-2H3,(H,20,21)\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H30F3N5O6/c1-16(2)21(23(37)27(28,29)30)31-20(36)15-35-19(17-6-4-3-5-7-17)14-18-22(25(35)39)32-26(40)34(24(18)38)9-8-33-10-12-41-13-11-33/h3-7,14,16,21H,8-13,15H2,1-2H3,(H,31,36)(H,32,40)\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r,3s)-2-(2,4-difluorophenyl)-3-(5-fluoropyrimidin-4-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(2,3-dichlorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1)\\\\C(=C/CN2CCCC2)\\\\c3ccccn3\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-chloro-2-[[(3s)-3-methyl-4-(phenylmethylsulfonyl)piperazin-1-yl]methyl]phenyl]acetic acid\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H13Cl2NO2S/c1-10-17(23-13-5-2-11(18)3-6-13)14-8-12(19)4-7-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-(pyridin-2-ylsulfamoyl)phenyl]acetamide\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[[1-[2-(7-methoxy-2-oxo-3,4-dihydroquinolin-1-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(2,2-dimethoxyethyl)-2,4,8-trioxo-6-phenyl-1h-pyrido[3,4-d]pyrimidin-7-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" comparison\\n\",\n        \"output\": \" comparison is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2nccc(Nc3cc(Cl)ccc3Cl)n2)cc1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)CC(=O)N[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4sc(Cl)c(Cl)c4[nH]3\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][N][Branch1][#Branch2][C][=Branch1][C][=O][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][C][N][Branch2][Ring1][Ring1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-phenyl-2,3,4,9-tetrahydro-1h-pyrido[5,4-b]indole-3-carboxylic acid\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H27N5O5S/c1-10(2)7-25-20-17(18(28)24(5)21(25)30)16(19(29)26-8-13(27)9-31-26)15(32-20)6-14-11(3)22-23-12(14)4/h10,13,27H,6-9H2,1-5H3,(H,22,23)/t13-/m0/s1\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[4-[[4-(4-fluorophenyl)piperazin-1-yl]sulfonylmethyl]oxan-4-yl]-n-hydroxyformamide\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" tert-butyl 4-[(3-pyridin-4-yl-1,2,4-oxadiazol-5-yl)methoxy]piperidine-1-carboxylate\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [1-(furan-2-carbonyl)piperidin-4-yl]-(4-methoxyphenyl)methanone\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)CCCCCCC(=O)Nc1ccc2c(c1)C(=O)C(=O)c3ccccc23\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)cc4\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H7BrClN3O3S2/c1-17-9-8(12-4-5(10)13-9)14-19(15,16)7-3-2-6(11)18-7/h2-4H,1H3,(H,12,14)\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(6-methoxynaphthalen-2-yl)propanoic acid\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H36N6O4/c1-18-16-33(17-19(2)37-18)27-30-25-22(26(31-27)32-9-12-36-13-10-32)5-6-23(29-25)20-4-7-24(35-3)21(14-20)15-28-8-11-34/h4-7,14,18-19,28,34H,8-13,15-17H2,1-3H3/t18-,19+\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring2][=C][O][C][=C][C][=C][Branch2][Ring1][S][N][C][=N][C][=N][C][NH1][N][=C][Branch1][#C][O][C][C][N][C][C][C][Branch1][C][O][C][C][Ring1][#Branch1][C][Ring2][Ring1][Ring1][=Ring1][#C][C][=C][Ring2][Ring1][#Branch2][Cl][C][=N][Ring2][Ring2][C]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H30N4O4S/c1-30-19-2-3-23-20(13-19)28(24(29)16-33-23)9-8-27-6-4-17(5-7-27)25-14-18-12-21-22(15-26-18)32-11-10-31-21/h2-3,12-13,15,17,25H,4-11,14,16H2,1H3\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-methyl-1-(phenylmethyl)pyrimidine-2,4-dione\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=N)c1cc2c(I)cccc2s1\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (1r,2s,3r,5r)-3-(7-butylamino-5-propylsulfanyltriazolo[5,4-d]pyrimidin-3-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-phenyl-1,2,3,4-tetrahydroisoquinoline\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[1-(7-chloroquinolin-4-yl)-5-methoxy-2-methylindol-3-yl]acetic acid\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[3-phenyl-3-(4-phenylpiperazin-1-yl)propyl]piperidin-4-yl]acetamide\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNCC[C@H](Oc1ccc(cc1)C(F)(F)F)c2ccccc2\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H23F2N3O4/c1-16-25(18-10-11-23-24(12-18)36-15-35-23)26(33)32(14-22(30)17-6-3-2-4-7-17)27(34)31(16)13-19-20(28)8-5-9-21(19)29/h2-12,22H,13-15,30H2,1H3/t22-/m0/s1\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1CCN(CC1)C(=O)[C@H](Cc2ccccc2)NC(=O)c3cc4cc(Cl)ccc4[nH]3\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [(3s)-oxolan-3-yl] n-[[3-[[3-methoxy-4-(1,3-oxazol-5-yl)phenyl]carbamoylamino]phenyl]methyl]carbamate\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" methyl 8-[(9,10-dioxophenanthren-3-yl)amino]-8-oxooctanoate\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)c1cc2cc(OCc3ccccc3)ccc2[nH]1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6,7-dimethoxy-n-(phenylmethyl)quinazolin-4-amine\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" mailbox\\n\",\n        \"output\": \" mailbox is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-methyl-6-(naphthalen-1-ylmethyl)-1-propan-2-ylpyrrolo[3,4-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H16FN5OS2/c1-8(6-22)18-12-11-13(19-14(17)24-11)21-15(20-12)23-7-9-4-2-3-5-10(9)16/h2-5,8,22H,6-7H2,1H3,(H3,17,18,19,20,21)/t8-/m1/s1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C30H31N3O5S/c1-38-28-18-24(30(35)32-39(36,37)26-9-3-2-4-10-26)13-14-25(28)20-33-16-15-22-11-12-23(17-27(22)33)29(34)31-19-21-7-5-6-8-21/h2-4,9-18,21H,5-8,19-20H2,1H3,(H,31,34)(H,32,35)\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H21ClN4O3S2/c1-12-14(18)4-3-5-15(12)27(24,25)20-17-19-13(11-26-17)10-16(23)22-8-6-21(2)7-9-22/h3-5,11H,6-10H2,1-2H3,(H,19,20)\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cn1cnc(c1Sc2ncnc3nc[nH]c23)[N+](=O)[O-]\\n\",\n        \"output\": \" 0.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=N][C][S][C][Branch1][#C][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][C][N][C][Ring2][Ring1][Ring2][=Ring1][S]\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1C=C(N=C2C=CC=CN12)N3CCOCC3\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=N][N][Branch1][P][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-(4-chlorophenyl)-1,3-benzoxazol-5-yl]propanoic acid\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-(azepan-1-yl)-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)OC(=O)N1CCC(CC1)Oc2ncnc3c2cnn3c4ccc(cc4F)S(=O)(=O)C\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4cccs4)C3=O\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H8O3/c14-9-5-3-7-11-12(9)13(15)8-4-1-2-6-10(8)16-11/h1-7,14H\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1N([Se]c2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" option\\n\",\n        \"output\": \" option is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H24N4O4/c1-18(2,3)25-17(23)22-10-6-14(7-11-22)24-12-15-20-16(21-26-15)13-4-8-19-9-5-13/h4-5,8-9,14H,6-7,10-12H2,1-3H3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H31N3/c1-20-17-21(2)19-23(18-20)27-25(24-8-3-4-9-26(24)30-27)12-16-28-13-6-5-7-22-10-14-29-15-11-22/h3-4,8-11,14-15,17-19,28,30H,5-7,12-13,16H2,1-2H3\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H8N2/c10-9-8-4-2-1-3-7(8)5-6-11-9/h1-6H,(H2,10,11)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" methyl 5-[(9,10-dioxophenanthren-3-yl)amino]-5-oxopentanoate\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H22F2N4O3/c1-8-5-24(6-9(2)23-8)17-13(20)15(22)12-16(14(17)21)25(10-3-4-10)7-11(18(12)26)19(27)28/h7-10,23H,3-6,22H2,1-2H3,(H,27,28)/t8-,9+\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][S][C][Branch2][Ring1][#Branch2][N][C][=Branch1][C][=O][C][=C][C][Branch1][#Branch2][S][C][=N][N][=C][N][Ring1][Branch1][C][=C][C][=C][Ring1][=N][N][=N][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)Nc1ccccc1C\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H16FN3S/c1-26-18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H28N4O3/c33-27(30-22-9-4-5-10-22)26(21-14-16-29-17-15-21)32(19-23-11-6-18-35-23)28(34)25-13-12-24(31-25)20-7-2-1-3-8-20/h1-3,6-8,11-18,22,26,31H,4-5,9-10,19H2,(H,30,33)\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-methylphenyl)prop-2-enamide\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-chloro-2-fluorophenyl)-6-methoxy-7-[[(3r)-1-methylpiperidin-3-yl]methoxy]quinazolin-4-amine\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(Cl)cc1C(=O)NCCc2ccc(cc2)S(=O)(=O)NC(=O)NC3CCCCC3\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" isoquinolin-1-amine\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][O][C][Branch2][Ring1][Ring2][C][N][Branch1][#Branch1][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][C][=N+1][Ring1][=Branch1][O-1][Branch1][=Branch1][C][Branch1][C][F][F][C][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H25F3N4O5/c1-16(2)22(23(35)26(27,28)29)32-21(34)14-33-20(18-9-6-12-30-13-18)11-10-19(24(33)36)31-25(37)38-15-17-7-4-3-5-8-17/h3-13,16,22H,14-15H2,1-2H3,(H,31,37)(H,32,34)\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][S][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-chloro-n-[(2s)-1-(4-hydroxypiperidin-1-yl)-1-oxo-3-phenylpropan-2-yl]-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCCN1CCN(CCCN2c3ccccc3Sc4ccc(Cl)cc24)CC1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H12N4OS/c15-11-10-9(18-8-4-2-1-3-5-8)6-7-17-14(10)20-12(11)13(16)19/h1-7H,15H2,(H2,16,19)(H,17,18)\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H11NO/c15-13(11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h1-10H,(H,14,15)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[[1-(4-chlorophenyl)cyclobutanecarbonyl]amino]-n-(4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-phenylethylhydrazine\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][=Branch2][O][C][C][N][Branch1][C][C][C][C][=C][Ring1][N]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[(3-methoxy-5-methylpyrazin-2-yl)sulfamoyl]-n-methyl-2-[4-(2-methylpropyl)phenyl]benzamide\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H22ClFN4O2/c1-26(2)7-4-8-28-19-10-14-17(11-18(19)27-3)23-12-24-20(14)25-13-5-6-16(22)15(21)9-13/h5-6,9-12H,4,7-8H2,1-3H3,(H,23,24,25)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H6N2/c1-2-4-8-7(3-1)5-9-6-10-8/h1-6H\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=NC(=C(NC1=O)c2ccccc2)c3ccc(CN4CCC(CC4)N5C(=O)Nc6ccccc56)cc3\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@@][Branch1][C][O][Branch2][Ring1][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][=C][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(C)C(=O)N[C@H]1CCCCNC1=O\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Ring1][C@H1][Branch1][C][O][C][C][C][C][C][N][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=Branch2][Ring1][=Branch2][=C][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][N][=C][Ring1][O][Ring1][#Branch1][N][C][C][O][C][C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCNC[C@H](O)COc1ccccc1C(=O)CCc2ccccc2\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)c1ccnc2sc(C(=O)N)c(N)c12\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][N][C][=C][C][=Branch2][Ring1][Branch2][=N][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" phenylmethyl n-[6-(3,5-dimethoxyphenyl)-2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyridin-3-yl]carbamate\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=N][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][N][=N][C][Ring1][O][C][=C][C][=C][S][Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" ethyl (e,4s)-4-[[(2r,5s)-2-[(4-fluorophenyl)methyl]-6-methyl-5-[(5-methyl1,2-oxazole-3-carbonyl)amino]-4-oxoheptanoyl]amino]-5-[(3s)-2-oxopyrrolidin-3-yl]pent-2-enoate\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H36N6O3/c1-31(2)25-19-24(28(35)29-20-5-7-21(8-6-20)33-13-15-37-16-14-33)30-27-23(25)17-22(36-4)18-26(27)34-11-9-32(3)10-12-34/h5-8,17-19H,9-16H2,1-4H3,(H,29,35)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" humor\\n\",\n        \"output\": \" humor is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" pasta\\n\",\n        \"output\": \" pasta is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1CC2(CCCC2)CC(=O)N1CCCCN3CCN(CC3)c4ncccn4\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H8N4O3S/c1-4-5(6(7(10)14)13-16-4)8(15)12-9-11-2-3-17-9/h2-3H,1H3,(H2,10,14)(H,11,12,15)\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[[1-[2-(6-fluoro-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][Branch1][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][Ring1][N]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-chloro-n-[(2s,3r)-4-dimethylamino-3-hydroxy-4-oxo-1-phenylbutan-2-yl]-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch2][Ring2][#C][C][C][O][C][=C][C][=C][Branch2][Ring1][S][C][C@H1][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][#Branch2][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1CCN(CC1)C(=O)c2cc3cc(Cl)ccc3[nH]2\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CSc1ccc(cc1)c2nc(c3ccc(F)cc3)c([nH]2)c4ccncc4\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(4-methoxyphenyl)-2-phenylsulfonylethanone\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(3-methylphenyl)-1-(2-morpholin-4-yl-2-pyridin-3-ylethyl)urea\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][C][=Branch1][C][=O][O][C][=C][Branch1][C][C][C][Branch1][C][O][=C][C][=C][Ring2][Ring1][C][Ring1][Branch2]\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5,7-dihydroxy-2-(4-hydroxyphenyl)chroman-4-one\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][N][=C][Branch2][Ring2][#Branch1][C][=C][Ring1][Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][N][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][Ring1][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(pyridin-3-ylmethyl)-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazin-6-amine\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C28H28N4O2/c1-30(2)15-17-12-13-32-22-11-7-5-9-19(22)24(23(32)14-17)26-25(27(33)29-28(26)34)20-16-31(3)21-10-6-4-8-18(20)21/h4-11,16-17H,12-15H2,1-3H3,(H,29,33,34)\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(=O)c1ccc(C2=CC3(CCNCC3)Oc4ccccc24)c(O)c1\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [5-[2-(tert-butylamino)-1-hydroxyethyl]-2-(4-methylbenzoyl)oxyphenyl] 4-methylbenzoate\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-6-methoxy-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)C(N1CCC(CC1)N2CCC(CC2)Oc3ccc(Cl)c(Cl)c3)c4ccccc4\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-amino-5-phenylthiophene-2-carboxamide\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=N][C][O][C][Branch1][Branch2][C][=C][O][C][=C][Ring1][Branch1][=C][Branch1][Branch2][C][O][C][=C][C][=Ring1][Branch1][C][Ring2][Ring1][Ring1][=Ring1][#C]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-chloro-5-methoxyphenyl)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinazolin-4-amine\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" S(c1ccccc1)c2ccc3ccccc3n2\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-cyclopentyl-2-[4-(3,4-difluorophenyl)-3-oxopyrazin-2-yl]sulfanylacetamide\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1,3-thiazol-5-ylmethyl n-[(2s,3s,5s)-3-hydroxy-5-[[(2s)-3-methyl-2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]butanoyl]amino]-1,6-di(phenyl)hexan-2-yl]carbamate\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H17N/c1-2-6-13(7-3-1)12-16-15-9-5-4-8-14(15)10-11-17-16/h1-9,16-17H,10-12H2\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1r,2s,3r,5r)-3-[7-[[(1r,2s)-2-(3,4-difluorophenyl)cyclopropyl]amino]-5-(3,3,3-trifluoropropylsulfanyl)triazolo[5,4-d]pyrimidin-3-yl]-5-(hydroxymethyl)cyclopentane-1,2-diol\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][Branch1][S][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][N][C][C][C][Branch1][C][O][Branch1][Branch1][C][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H]1CN[C@@H]2[C@@H](C1)O[C@]3(CC[C@H]4[C@@H]5CC=C6C[C@@H](O)CC[C@]6(C)[C@H]5CC4=C3C)[C@@H]2C\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][N][Branch2][Branch1][=Branch2][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring1][N][C][=C][C][=C][C][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][O][C][Ring1][O][=Ring1][#Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][=C][=Ring1][=Branch2][C][C][Ring2][Ring2][Branch2]\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[4-[(3-methylphenyl)amino]pyridin-3-yl]sulfonyl-1-propan-2-ylurea\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H26ClN5O4/c24-15-1-3-19-18(11-15)29(22(31)14-33-19)10-9-28-7-5-16(6-8-28)25-12-17-2-4-20-23(26-17)27-21(30)13-32-20/h1-4,11,16,25H,5-10,12-14H2,(H,26,27,30)\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][NH1][Ring1][=C]\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H21N3/c1-18(2)12-13-19(16-10-6-7-11-17-16)14-15-8-4-3-5-9-15/h3-11H,12-14H2,1-2H3\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][O][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][O][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][N][=Ring1][=N][C][=N][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H17N5S/c1-12(2)16-10(13)15-11(14)17(12)8-4-6-9(18-3)7-5-8/h4-7H,1-3H3,(H4,13,14,15,16)\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1c(NC(=O)NCCCCN2CCCC2)snc1OCc3c(F)cc(Br)cc3F\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C31H42N6O4/c1-23(2)41-25-10-8-24(9-11-25)34-31(38)37-17-15-36(16-18-37)30-26-20-28(39-3)29(21-27(26)32-22-33-30)40-19-7-14-35-12-5-4-6-13-35/h8-11,20-23H,4-7,12-19H2,1-3H3,(H,34,38)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H14N4O2/c26-21-17-14-22-25(16-10-5-2-6-11-16)19(17)23-20(18-12-7-13-27-18)24(21)15-8-3-1-4-9-15/h1-14H\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@H1][Branch1][C][C][C@@H1][Branch1][Ring1][C][O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" knight\\n\",\n        \"output\": \" knight is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H22O3/c1-11-6-7-12(2)13(10-11)18-9-5-8-15(3,4)14(16)17/h6-7,10H,5,8-9H2,1-4H3,(H,16,17)\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][C][C@H1][Branch2][Ring2][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][O][C][Branch1][C][C][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H22F3N3O5S/c1-12(2)17(18(28)20(21,22)23)24-16(27)11-26-15(13-7-5-4-6-8-13)10-9-14(19(26)29)25-32(3,30)31/h4-10,12,17,25H,11H2,1-3H3,(H,24,27)\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][Branch1][P][C][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][=Branch2][O][C][C@H1][Branch1][C][O][C][O][=C][Ring1][N]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][N][C][Ring1][N][=Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-phenyl-n-(phenylmethyl)ethanamine\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(Cn1cncn1)(Cn2cncn2)c3ccc(F)cc3F\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch2][Ring1][=C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][S][Ring1][=Branch1][C][C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][C][Br][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C@@H1][Branch2][Ring1][=C][C][C][=C][C][=C][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=C][Ring1][P][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-methoxyphenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][N][C][C][=C][NH1][C][=C][C][=C][Branch1][#Branch2][O][C][C][=C][C][=C][S][Ring1][Branch1][C][=C][Ring1][S][Ring1][=N]\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1cccc2Oc3ccccc3C(=O)c12\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch2][Ring1][Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=O][C][C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4s)-4-amino-5-[(4,4-dimethylcyclohexyl)amino]-5-oxopentanoic acid\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Branch1][=Branch1][S][C][C][C][O][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][N][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H25NO6/c1-12(24)23-16-8-6-13-10-19(27-3)21(28-4)22(29-5)20(13)14-7-9-18(26-2)17(25)11-15(14)16/h7,9-11,16H,6,8H2,1-5H3,(H,23,24)\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][C][S][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,3,7-trimethylpurine-2,6-dione\\n\",\n        \"output\": \" -0.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" snowflake\\n\",\n        \"output\": \" snowflake is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=N][C][=C][Ring2][Ring1][Ring1][F]\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Oc2ccc(Cl)cc2)c3c(NS(=O)(=O)C)cccc3n1CC(=O)O\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][C][=C][Ring1][#C][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[2-oxo-3-[4-(5-phenylpentylsulfanyl)phenoxy]propoxy]benzoic acid\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" germany\\n\",\n        \"output\": \" germany is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch2][Ring2][#Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring2][Ring1][S][O]\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][NH1][N][=C][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=C][C][=Branch2][Ring1][=N][=N][C][=C][Branch1][=N][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][N][Ring1][Branch2][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[(1r,2r)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]-4-phenylpiperidin-4-ol\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1C(=O)NC(=O)C(C)(C2=CCCCC2)C1=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1nccn1CCC(C(=O)N)(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H11NO/c1-8(11)10(2)9-6-4-3-5-7-9/h3-7H,1-2H3\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][S][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][N][C][C][C][C][C][C][C][N][Ring1][=Branch1][C][C][Ring2][Ring1][Ring1][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H30O5/c1-12-8-14-15-5-7-22(27,18(26)11-23)21(15,3)10-17(25)19(14)20(2)6-4-13(24)9-16(12)20/h4,6,9,12,14-15,17,19,23,25,27H,5,7-8,10-11H2,1-3H3/t12-,14-,15-,17-,19+,20-,21-,22-/m0/s1\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(cc(OC)c1OC)C(=O)c2cc(Cl)ccc2N\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-[(3r)-3-(3,4-dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]-4-phenylpiperidine-4-carboxamide\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,2-dimethyl-n-[(3s)-2-oxoazepan-3-yl]propanamide\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" adult\\n\",\n        \"output\": \" adult is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][=C][N][C][C][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H13N3O/c1-11(8-5-3-2-4-6-8)7-9(15)13-10(12)14-11/h2-6H,7H2,1H3,(H3,12,13,14,15)\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H19N3O2/c1-17-5-7-18(8-6-17)15(19)14-10-11-9-12(20-2)3-4-13(11)16-14/h3-4,9-10,16H,5-8H2,1-2H3\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-methyl-n-phenylacetamide\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H12N2O2/c1-2-13-10(14)9(12-11(13)15)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H,12,15)\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=N][N][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(cc1F)N2C=CN=C(SCC(=O)NC3CCCC3)C2=O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H13N3/c1-11-6-2-4-8-13(11)18-15-12-7-3-5-9-14(12)16-10-17-15/h2-10H,1H3,(H,16,17,18)\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-thiophen-3-ylphenanthrene-9,10-dione\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring2][=Branch2][C][=Branch1][C][=O][N][Branch1][=C][C][C@H1][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][P][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F]\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cnc(nc1N(C)C)c2ccccn2\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C7H5ClN2/c8-6-2-1-3-7-5(6)4-9-10-7/h1-4H,(H,9,10)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(CO)(CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)sc13\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" jason\\n\",\n        \"output\": \" jason is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][\\\\C][=Branch1][#C][=C][\\\\C][C][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][\\\\C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-acetamido-n-[4-chloro-3-(trifluoromethyl)phenyl]-9-azabicyclo[3.3.1]nonane-9-carboxamide\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CCCN1c2ccccc2Sc3ccccc13\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(3-amino-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H9ClN2/c14-11-6-4-10(5-7-11)12-9-16-8-2-1-3-13(16)15-12/h1-9H\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Nc1cccc(NC(=O)c2ccccc2)n1)c3ccccc3\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H22ClNO/c1-14(16-8-5-10-17(13-16)21-2)20-12-6-9-15-7-3-4-11-18(15)19/h3-5,7-8,10-11,13-14,20H,6,9,12H2,1-2H3/t14-/m1/s1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCC(=O)N1CCN(CC1)c2nnc(c3ccccc3)c4ccccc24\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m1/s1\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H31N5O4/c1-33-20-5-2-17-3-7-24(32)30(21(17)14-20)13-12-29-10-8-18(9-11-29)26-15-19-4-6-22-25(27-19)28-23(31)16-34-22/h2,4-6,14,18,26H,3,7-13,15-16H2,1H3,(H,27,28,31)\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H10F2N2O2/c14-10-3-1-8(5-11(10)15)6-17-7-9(13(16)19)2-4-12(17)18/h1-5,7H,6H2,(H2,16,19)\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(benzoylamino)-3-methylbenzamide\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(Nc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)C(=O)CN2C3=NCCN3c4ccccc24\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][#C][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1oc(nc1CCOc2ccc(C[C@H](Nc3ccccc3C(=O)c4ccccc4)C(=O)O)cc2)c5ccccc5\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=Branch1][=Branch1][=N][C][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][N][C][C@@H1][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][Branch1][Ring2][N][C][=O][=C][Ring1][#Branch2][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H20F6N4O5/c1-11(2)15(16(33)21(25,26)27)30-14(32)9-31-17(12-6-4-3-5-7-12)28-8-13(18(31)34)29-19(35)36-10-20(22,23)24/h3-8,11,15H,9-10H2,1-2H3,(H,29,35)(H,30,32)\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H32ClN3O/c25-22-2-1-15(12-28-13-19-7-20(28)11-26-19)6-21(22)23(29)27-14-24-8-16-3-17(9-24)5-18(4-16)10-24/h1-2,6,16-20,26H,3-5,7-14H2,(H,27,29)/t16?,17?,18?,19-,20-,24?/m0/s1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14ClN3O/c1-19-13-4-2-3-5-14(13)20(16(19)18)10-15(21)11-6-8-12(17)9-7-11/h2-9,18H,10H2,1H3\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(C1CCN(CCC(N2CCC(CC2)C(=O)C)c3ccccc3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H20N2O2/c1-13-12-17(20-14(2)22)16-10-6-7-11-18(16)21(13)19(23)15-8-4-3-5-9-15/h3-11,13,17H,12H2,1-2H3,(H,20,22)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OCCOCCN1CCN(CC1)C(c2ccccc2)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=Branch2][Ring1][Branch1][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C33H36N4O4S/c1-23-28(35-33(42-23)37-19-17-36(2)18-20-37)16-21-41-26-14-12-24(13-15-26)22-30(32(39)40)34-29-11-7-6-10-27(29)31(38)25-8-4-3-5-9-25/h3-15,30,34H,16-22H2,1-2H3,(H,39,40)/t30-/m0/s1\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)c1c(nc2cc(C)ccn12)c3ccccc3\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H15N3OS/c1-6-5-7(2)15-13-9(6)10(14)11(18-13)12(17)16-8-3-4-8/h5,8H,3-4,14H2,1-2H3,(H,16,17)\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H33ClN4O2S/c26-20-8-9-24-22(19-20)30(21-5-1-2-6-23(21)33-24)12-4-11-28-13-15-29(16-14-28)17-18-32-25(31)7-3-10-27/h1-2,5-6,8-9,19H,3-4,7,10-18,27H2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfonyl-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H11Cl2N3O2/c1-23-13-5-4-10(9-3-2-6-20-14(9)13)16(22)21-15-11(17)7-19-8-12(15)18/h2-8H,1H3,(H,19,21,22)\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][Branch1][C][N][N][=C][Branch1][C][N][N][=C][Ring1][Branch2][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-methyl-5-[[3-(trifluoromethyl)benzoyl]amino]phenyl]quinoline-6-carboxamide\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][Branch1][=C][O][N][=C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[[(4-methylpyridin-2-yl)amino]methyl]phenol\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][S][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(4-amino-2-ethylimidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNCCC(Oc1ccccc1OC)c2ccccc2\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [5-[2-[(2r,6s)-2,6-dimethylmorpholin-4-yl]-4-morpholin-4-ylpyrido[5,6-e]pyrimidin-7-yl]-2-methoxyphenyl]methanol\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(c1ncccc1CNc2nc(Nc3ccc4NC(=O)Cc4c3)ncc2C(F)(F)F)S(=O)(=O)C\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cn1c2ccccc2c3cc(NC(=O)CCc4ccncc4)ccc13\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-aminophenyl)-4-(1,3-thiazol-2-yl)benzamide\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Ring1][O][N][Ring2][Ring1][=Branch1][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring1][=N]\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-(furan-2-carbonyl)piperazin-1-yl]-2-phenylsulfanylethanone\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H21N3O2S/c1-15-20(18,19)10-11-4-5-14-13(8-11)12(9-16-14)6-7-17(2)3/h4-5,8-9,15-16H,6-7,10H2,1-3H3\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C@@H1][Branch2][Ring2][Branch1][N][C][=C][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][Branch1][#Branch2][C][=Branch1][C][=O][N][Branch1][C][C][C][=C][Ring1][O][O][C][=Branch1][C][=O][C][Ring2][Ring1][C][=O][C][O][C][Branch1][C][C][=C][C][=Ring1][=Branch1]\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-methyl-4-phenylsulfonylbenzene\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][Ring1][=Branch1][N][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H31N3O2/c1-31-25-11-5-4-10-24(25)29-18-16-28(17-19-29)15-7-6-14-27-26(30)23-13-12-21-8-2-3-9-22(21)20-23/h2-5,8-13,20H,6-7,14-19H2,1H3,(H,27,30)\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 1-methyl-4-phenylpiperidine-4-carboxylate\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" booklet\\n\",\n        \"output\": \" booklet is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch2][Ring1][#C][C][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H11F2N3O4/c10-9(11)6(16)4(3-15)18-7(9)14-2-1-5(12)13-8(14)17/h1-2,4,6-7,15-16H,3H2,(H2,12,13,17)/t4-,6-,7-/m1/s1\\n\",\n        \"output\": \" -1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4cccnn34)cc1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27ClN2O5/c1-15(27)25-20-4-3-18(28)11-22(20)30-14-19(29)13-26-8-6-23(7-9-26)12-16-10-17(24)2-5-21(16)31-23/h2-5,10-11,19,28-29H,6-9,12-14H2,1H3,(H,25,27)/t19-/m0/s1\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][NH1][C][=Branch1][Branch2][=C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][N][Branch2][Ring1][S][C][C][C][N][Branch2][Ring1][Ring2][C][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][N][C][Ring2][Ring1][=Branch2][=C][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccccc1C2=C3C=CC(=O)C=C3Oc4cc(O)ccc24\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)CCOC(=O)C1(CCCC1)c2ccccc2\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(CNc2nc3ccccc3[nH]2)cc(OC)c1OC\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][N][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][N][=C][Branch1][P][C][=C][Branch1][=Branch1][N][Branch1][C][C][C][C][Ring1][=Branch2][=C][Ring2][Ring1][Ring2][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)15-8-13(18)12-7-11(17)5-6-14(12)19-15/h1-8,16-17H\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Br][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3ccncc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCSCCCNCCc1cccc(Cl)c1Cl)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2,3-difluorophenyl)-2-[5-[[7-[3-(ethyl-(2-hydroxyethyl)amino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][Branch1][N][N][C][C][N][C][Branch1][C][C][C][Ring1][#Branch1][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=Branch1][S][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring2][Ring1][=Branch1][=Ring1][#Branch2][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[(3,4-difluorophenyl)methyl]-6-oxopyridine-3-carboxamide\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[3-phenyl-3-[1-(phenylmethyl)piperidin-4-yl]propyl]piperidin-4-yl]acetamide\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" [O-][N+](=O)c1cccc(c1)c2ccc(OCC(CCc3ccc(cc3)C(=O)N4CCCC4)N5C(=O)CCCC5=O)cc2\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" chard\\n\",\n        \"output\": \" chard is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc3ccccc3\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COCC1=C(N2[C@H](SC1)[C@H](NC(=O)\\\\C(=N/OC)\\\\c3csc(N)n3)C2=O)C(=O)OC(C)OC(=O)OC(C)C\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[1-[[(1r)-1-[3-[(e)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl]-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl]sulfanylmethyl]cyclopropyl]acetic acid\\n2-[1-[[(1r)-1-[3-[2-(7-chloroquinolin-2-yl)ethenyl]phenyl]-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl]sulfanylmethyl]cyclopropyl]acetic acid\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NCCCC(=O)OCCN1CCN(CCCN2c3ccccc3Sc4ccc(Cl)cc24)CC1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" eight\\n\",\n        \"output\": \" eight is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H23FN2O4S2/c21-18-12-22-20(28-18)23-19(24)17(11-13-7-9-27-10-8-13)14-1-3-15(4-2-14)29(25,26)16-5-6-16/h1-4,12-13,16-17H,5-11H2,(H,22,23,24)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-[(1r)-2-[2-[3-[2-(4-ethoxyphenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H17FN4O2/c23-16-11-5-7-13-18(16)25-22(29)27-20-21(28)24-17-12-6-4-10-15(17)19(26-20)14-8-2-1-3-9-14/h1-13,20H,(H,24,28)(H2,25,27,29)/t20-/m1/s1\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][NH1][C][=Branch1][Branch2][=N][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][S][C][=N][Ring1][Branch1]\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=N][C][Branch1][C][Br][=C][N][=C][Ring1][#Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H](CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)cnc13\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(C(=O)Nc1oc(nn1)C(=O)Nc2ccc(cc2)N3CCOCC3)c4ccc(Cl)cc4\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H21BrN2O3/c1-12(19)18-8-6-17(7-9-18)10-14(20)11-21-15-4-2-13(16)3-5-15/h2-5,14,20H,6-11H2,1H3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@@][Branch1][C][O][Branch2][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=S][N][Ring1][Branch2]\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-hydroxy-2-(4-methylphenyl)sulfonyl-2,3,1-benzodiazaborinine\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[8-(dimethylaminomethyl)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]-4-(1-methylindol-3-yl)pyrrole-2,5-dione\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch2][Ring1][P]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H23ClN2O5S/c1-15-12-23(29(26,27)18-5-3-2-4-6-18)10-9-22(15)13-16-11-17(21)7-8-19(16)28-14-20(24)25/h2-8,11,15H,9-10,12-14H2,1H3,(H,24,25)\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[5-(thiophen-2-ylmethoxy)-1h-indol-3-yl]propan-2-amine\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-5-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][=Branch1][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][C][=C][C][=C][C][=N][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" input\\n\",\n        \"output\": \" input is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H](CO)Nc1nc(SCc2cccc(Cl)c2)nc3nc(N)sc13\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [4-(4-chlorobenzoyl)piperidin-1-yl]-cyclopropylmethanone\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][O][C][=C][Branch1][C][C][C][O][C][Branch1][C][C][=C][C][=Ring1][=Branch1][C][=C][Ring1][S][Ring1][O]\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccccc1NC(=O)c2ccc(CNC(=O)OCc3cccnc3)cc2\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,1-dioxo-3-(phenylmethyl)-6-(trifluoromethyl)-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][C][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][S][N][=N][C][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][Branch1][C][Br][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)Cn1cnc2c(N)nc3ccccc3c12\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nc2ccccc2n1C(=O)c3ccccc3\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H19N5/c1-10-5-7-11(8-6-10)13-12-14(17)18-9-19-15(12)21(20-13)16(2,3)4/h5-9H,1-4H3,(H2,17,18,19)\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H15N3O2/c20-15-11-14(18-7-9-21-10-8-18)17-16-13-4-2-1-3-12(13)5-6-19(15)16/h1-6,11H,7-10H2\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][=C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][Ring2][C][Ring1][Branch1][N][Branch1][C][C][C][=N][C][=C][Ring2][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H10F3N5/c11-10(12,13)9-15-14-7-3-4-8(16-18(7)9)17-5-1-2-6-17/h3-4H,1-2,5-6H2\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H10BrN3O4/c14-9-3-1-2-4-10(9)15-13(19)16-11-6-5-8(17(20)21)7-12(11)18/h1-7,18H,(H2,15,16,19)\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n'-[3-[[5-bromo-2-[[3-(pyrrolidine-1-carbonylamino)phenyl]amino]pyrimidin-4-yl]amino]propyl]-2,2-dimethylpropanediamide\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H22ClN3O/c1-3-24(4-2)13-14-11-16(6-8-20(14)25)23-18-9-10-22-19-12-15(21)5-7-17(18)19/h5-12,25H,3-4,13H2,1-2H3,(H,22,23)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-phenylpyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1Oc2ccccc2C=C1c3ccccc3\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H13F3O4/c1-22-12-5-2-10(3-6-12)13-8-11(16(17,18)19)4-7-14(13)23-9-15(20)21/h2-8H,9H2,1H3,(H,20,21)\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][S][=Ring1][N]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-[(2,3-dichloro4h-thieno[2,3-d]pyrrole-5-carbonyl)amino]-2-oxo-3,4-dihydroquinolin-1-yl]acetic acid\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][Branch1][#C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(9h-carbazol-4-yloxy)-3-[2-(2-methoxyphenoxy)ethylamino]propan-2-ol\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H](Oc1cccc2ncnc(Nc3ccc4c(cnn4Cc5cscn5)c3)c12)C(=O)N6CCOCC6\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidin-1-yl]-2-phenylacetic acid\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H](N)COc1c(C)cccc1C\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-[[[1-[2-(6-hydroxy-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OCCCN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][O][C][=Branch1][C][=O][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][Branch1][S][C][S][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][=C][Ring1][P]\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][C][=C][Branch2][Ring1][#C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][Ring1][P][N][Ring2][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C1NC(Cc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H8ClNO2S/c12-8-3-1-7(2-4-8)11-13-9(6-16-11)5-10(14)15/h1-4,6H,5H2,(H,14,15)\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" columnist\\n\",\n        \"output\": \" columnist is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H24N2O6/c1-11(2)10-28-20(24)17-13(4)21-12(3)16(19(23)27-5)18(17)14-8-6-7-9-15(14)22(25)26/h6-9,11,18,21H,10H2,1-5H3\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][Branch1][=C][N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Ring1][#C]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-tert-butyl-3-[[5-methyl-2-[[4-(4-methylpiperazin-1-yl)phenyl]amino]pyrimidin-4-yl]amino]benzenesulfonamide\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(Cl)c(Nc2ncnc3cc(OCC4CCN(C)CC4)c(OC)cc23)c1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@]12CCC(=O)C=C1CC[C@H]3[C@@H]4CC[C@](O)(C(=O)CO)[C@@]4(C)CC(=O)[C@H]23\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H34O7/c1-15(27)32-17-3-8-23(14-26)19-4-7-22(2)18(16-11-21(28)31-13-16)6-10-25(22,30)20(19)5-9-24(23,29)12-17/h11,14,17-20,29-30H,3-10,12-13H2,1-2H3/t17-,18+,19-,20+,22+,23-,24-,25-/m0/s1\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C]\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H17NO3S/c1-9-2-4-14(5-3-9)13(15)12-11-10(8-18-12)16-6-7-17-11/h8-9H,2-7H2,1H3\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H17BrClNO2/c17-14-3-6-16(13(9-14)10-19-7-8-20)21-11-12-1-4-15(18)5-2-12/h1-6,9,19-20H,7-8,10-11H2\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][Ring1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1-methylindol-2-yl)-(4-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H28N4O5S/c1-14(2)11-30-25-22(23(33)28(3)26(30)35)21(24(34)29-12-18(31)19(32)13-29)20(36-25)10-15-8-9-27-17-7-5-4-6-16(15)17/h4-9,14,18-19,31-32H,10-13H2,1-3H3/t18-,19+\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=Branch2][Ring1][C][=C][C][=Branch1][C][=O][N][Ring1][#Branch1][C][C][=C][C][=C][C][=N][Ring1][=Branch1][N][N][Branch1][Branch1][C][Ring1][S][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=N][C][=C][C][=C][Branch1][S][\\\\C][=C][\\\\C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][Ring1][P][S][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)cc4Cl\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H9ClO3/c1-7-10(12(14)15)6-11(16-7)8-2-4-9(13)5-3-8/h2-6H,1H3,(H,14,15)\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][C][C][C][C][N][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(C1CCN(CC1)c2nnc(s2)n3cccc3)N4CCc5ccccc5C4\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cn1cnc(c2ccccc2)c1c3nc4c(N)ncnc4s3\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H6N6O2/c1-11-6(14)12-2-8-3(4(7)13)5(12)9-10-11/h2H,1H3,(H2,7,13)\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CC1CCn2c(C1)c(C3=C(C(=O)NC3=O)c4cn(C)c5ccccc45)c6ccccc26\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-chlorophenyl)imidazo[1,2-a]pyridine\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" propan-2-yl 4-[5-methyl-6-(2-methylpyridin-3-yl)oxypyrimidin-4-yl]oxypiperidine-1-carboxylate\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(CNC(=O)C2CCCN2S(=O)(=O)c3ccc(F)cc3)cc1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H28N2O4S2/c25-18-8-7-17(21-20(18)24-22(27)30-21)19(26)15-23-10-14-29-13-4-11-28-12-9-16-5-2-1-3-6-16/h1-3,5-8,19,23,25-26H,4,9-15H2,(H,24,27)/t19-/m0/s1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(OC2CCN(C)CC2)c3c(Nc4cccc5OCCOc45)ncnc3c1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (3r,5r)-7-[(1s,2s,6r,8s,8ar)-2,6-dimethyl-8-[(2s)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" c1ccc(nc1)c2nc3ccccc3[nH]2\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" [O-][S+](CCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" quicksand\\n\",\n        \"output\": \" quicksand is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][=N][C][=N][C][=C][C][Branch1][N][O][C][C][C][N][C][C][C][C][Ring1][Branch1][=C][C][Branch1][#Branch2][O][C][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-morpholin-4-ylpyrido[2,1-b]pyrimidin-4-one\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1C2=NC(=O)N(C)C(=O)C2=Cc3ccccc13\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H16N2O2/c1-3-21-17(20)16-15(13-7-5-4-6-8-13)18-14-11-12(2)9-10-19(14)16/h4-11H,3H2,1-2H3\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H17F3N2O2/c1-12-6-7-18-16(10-12)20(13(2)27(18)11-19(28)29)14-8-9-26-21-15(14)4-3-5-17(21)22(23,24)25/h3-10H,11H2,1-2H3,(H,28,29)\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C@H1][C][N][Branch1][S][C][C][C][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][C@H1][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][N][C][=C][Ring1][Branch2][O][C]\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H24N2O2/c1-3-9(7-13)11-5-6-12-10(4-2)8-14/h9-14H,3-8H2,1-2H3\\n\",\n        \"output\": \" -1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][\\\\N][=C][Branch2][Ring2][Branch2][\\\\C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=N][C][=C][Ring1][#Branch1][Cl][/C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][N]\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H26FN3O2/c1-26-12-14-27(15-13-26)11-2-16-28-21-9-5-19(6-10-21)23-17-22(25-29-23)18-3-7-20(24)8-4-18/h3-10,17H,2,11-16H2,1H3\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H26F3N3O3S/c1-14(2)13-30-22-19(20(31)28(3)23(30)33)18(21(32)29-10-6-7-11-29)17(34-22)12-15-8-4-5-9-16(15)24(25,26)27/h4-5,8-9,14H,6-7,10-13H2,1-3H3\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H28N6O3S/c31-22(19-5-9-30(10-6-19)24-26-25-23(34-24)29-7-1-2-8-29)28-13-11-27(12-14-28)16-18-3-4-20-21(15-18)33-17-32-20/h1-4,7-8,15,19H,5-6,9-14,16-17H2\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=C][Ring2][Ring1][Branch2][C][=C][Ring2][Ring1][N][O][C]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" c1ccc2ncncc2c1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(2,4-difluorophenoxy)-5-methoxy-2-pyridin-2-ylpyrimidine\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCCSCCNCCc1cccc(Cl)c1)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H20N6O/c1-11(2)24-12(3)21-10-16(24)15-8-9-20-18(23-15)22-14-6-4-13(5-7-14)17(19)25/h4-11H,1-3H3,(H2,19,25)(H,20,22,23)\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H22N4/c1-23-12-14-24(15-13-23)17-8-6-16(7-9-17)22-20-10-11-21-19-5-3-2-4-18(19)20/h2-11H,12-15H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C1CCN(CCC(c2ccccc2)c3ccccc3)CC1)C(=O)c4ccncc4\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H27Cl2N3O4S/c24-21-7-6-20(16-22(21)25)32-19-10-12-27(13-11-19)18-8-14-28(15-9-18)33(30,31)26-23(29)17-4-2-1-3-5-17/h1-7,16,18-19H,8-15H2,(H,26,29)\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch2][Branch1][Ring1][C][C][C][N][Branch2][Ring2][#Branch1][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][C][C][Ring2][Ring1][O][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,2,2-trifluoroethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-thiophen-2-ylpyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(4-bromo-2-fluorophenyl)-6-methoxy-7-[[(3r)-1-methylpiperidin-3-yl]methoxy]quinazolin-4-amine\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1C=CN=C2C=CC=CN12\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][C][C][N][C][C@H1][Ring1][=Branch1][C][O][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(C(=O)CN2C=C(C=CC2=O)C(F)(F)F)c(C)n1Cc3ccccc3\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" rutabaga\\n\",\n        \"output\": \" rutabaga is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H21NO2/c1-12(2)17-10-14(18)11-19-16-9-5-7-13-6-3-4-8-15(13)16/h3-9,12,14,17-18H,10-11H2,1-2H3/t14-/m1/s1\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2-formylphenyl)boronic acid\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" range\\n\",\n        \"output\": \" range is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H38N8O3/c1-5-34-27(37)33(3)22-17-28-26(31-24(22)35(34)20-8-6-7-9-20)30-21-11-10-18(16-23(21)38-4)25(36)29-19-12-14-32(2)15-13-19/h10-11,16-17,19-20H,5-9,12-15H2,1-4H3,(H,29,36)(H,28,30,31)\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][C][O][C][=C][C][=C][C][=Branch2][Ring1][#Branch2][=N][C][=Branch1][Branch2][=N][C][Ring1][=Branch1][=N][Ring1][#Branch2][N][C][C@@H1][Branch1][C][C][O][C@@H1][Branch1][C][C][C][Ring1][Branch2][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s,3s)-2-(3-chlorophenyl)-3,5,5-trimethylmorpholin-2-ol\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCCN(CC1)C(c2ccccc2)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)COCC(CN(Cc1ccccc1)c2ccccc2)N3CCCC3\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H23N3O2/c1-15(2)11-25-20-14-24(13-19(20)21(26)23(3)22(25)27)12-17-9-6-8-16-7-4-5-10-18(16)17/h4-10,13-15H,11-12H2,1-3H3\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H15N/c15-14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10,14H,11,15H2\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H26F3N5O4/c1-16(2)22(23(36)26(27,28)29)33-21(35)15-34-20(17-8-4-3-5-9-17)12-11-19(24(34)37)32-25(38)31-14-18-10-6-7-13-30-18/h3-13,16,22H,14-15H2,1-2H3,(H,33,35)(H2,31,32,38)\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H27N3O5S2/c1-22(13-12-16-4-6-17(7-5-16)20-28(2,23)24)14-15-27-19-10-8-18(9-11-19)21-29(3,25)26/h4-11,20-21H,12-15H2,1-3H3\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][=Branch1][C][=O][C][=C][Branch1][O][O][C][=Branch1][=Branch1][=C][C][Ring1][=Branch1][=O][O][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H11NO2/c18-16(19)13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10H,(H,18,19)\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][C][C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][=C][Ring1][P]\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-(piperidin-4-ylmethyl)benzamide\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OCCN(C(=O)CNC(=O)c1cc2cc(Cl)ccc2[nH]1)c3ccccc3\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][N][Branch1][O][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][N][C][C][=C][O][N][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H21NO4/c1-2-27-22(26)20(14-15-10-12-17(24)13-11-15)23-21(25)19-9-5-7-16-6-3-4-8-18(16)19/h3-13,20,24H,2,14H2,1H3,(H,23,25)/t20-/m0/s1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H14ClN3O4/c1-10(16-8-11-4-2-3-5-15(11)29-16)25-21(28)17-18(20(27)24-25)23-14-9-12(22)6-7-13(14)19(17)26/h2-10H,1H3,(H,23,26)(H,24,27)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H12O4/c1-9-13-7-6-12(18)8-14(13)20-16(19)15(9)10-2-4-11(17)5-3-10/h2-8,17-18H,1H3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][N][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][#C][N][=C][N][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H40O6/c1-6-25(4,5)24(30)31-21-12-15(2)11-17-8-7-16(3)20(23(17)21)10-9-18(26)13-19(27)14-22(28)29/h7-8,11,15-16,18-21,23,26-27H,6,9-10,12-14H2,1-5H3,(H,28,29)/t15-,16-,18+,19+,20-,21-,23-/m0/s1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H27Cl2N3O4S/c24-21-7-6-19(16-22(21)25)32-18-10-14-27(15-11-18)17-8-12-28(13-9-17)23(29)26-33(30,31)20-4-2-1-3-5-20/h1-7,16-18H,8-15H2,(H,26,29)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H21FN2O2/c21-18-8-6-16(7-9-18)19(24)17-10-12-23(13-11-17)20(25)22-14-15-4-2-1-3-5-15/h1-9,17H,10-14H2,(H,22,25)\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch2][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=N][O][N][=C][Ring1][=Branch2][Ring1][Branch1][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-ethyl-n-[1-[3-(1-ethylsulfonylpiperidin-4-yl)-3-phenylpropyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H9N3O2S/c10-9-8(6-11-12-9)15(13,14)7-4-2-1-3-5-7/h1-6H,(H3,10,11,12)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)c1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20F3NO5S/c1-3-23(4-2)29(26,27)15-8-5-13(6-9-15)16-11-14(19(20,21)22)7-10-17(16)28-12-18(24)25/h5-11H,3-4,12H2,1-2H3,(H,24,25)\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][Branch1][Ring1][O][C][C][=C][C][Branch1][C][Br][=C][Ring1][=Branch2][O][C]\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-8,16-17H\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)c2ccc3N=CN(C(=O)c3c2)c4cc(ccc4C)C(=O)NC5CCC5\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H17NO2/c14-12(11-4-2-1-3-5-11)10-13-6-8-15-9-7-13/h1-5,12,14H,6-10H2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H28N2O4S2/c25-18-8-7-17(21-20(18)24-22(27)30-21)19(26)15-23-10-4-13-29-14-12-28-11-9-16-5-2-1-3-6-16/h1-3,5-8,19,23,25-26H,4,9-15H2,(H,24,27)/t19-/m0/s1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H25NO3/c1-15(19(23)16-7-9-18(22)10-8-16)21-13-11-20(24,12-14-21)17-5-3-2-4-6-17/h2-10,15,19,22-24H,11-14H2,1H3/t15-,19+/m1/s1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch2][Branch1][=Branch1][C][C][C][N][Branch2][Ring2][#Branch2][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][=Branch2][C][C][Ring2][Ring1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3cc(C)ccc3F)c2cc1OC\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[(7-chloroquinolin-4-yl)amino]-2-(diethylaminomethyl)phenol\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][N][=C][N][=C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring1][#C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccc(cc1)S(=O)(=O)Nc2ccccn2\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][Branch1][C][N][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=C(CCC(=O)O)C(=O)Oc2c(C)c(O)ccc12\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3,3,3-trifluoro-2-hydroxy-2-methyl-n-(4-phenylsulfonylphenyl)propanamide\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-(2-methylpropyl)phenyl]-n-methylsulfonylpropanamide\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][S][C][C][C][C][C][C][=Ring1][=Branch1][C][=Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (4-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-fluoro-4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-(1-methylpiperidin-4-yl)benzamide\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3-chloro-2-fluorophenyl)-7-methoxy-6-(1-methylsulfonylpiperidin-4-yl)oxyquinazolin-4-amine\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-nitroaniline\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CC\\\\C=C\\\\1/c2ccccc2Sc3ccc(Cl)cc13\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][Ring1][O][C][=C][C][=Branch1][Ring2][=C][Ring1][Branch2][C][=C][C][=C][N][=C][Branch1][C][N][N][=C][Ring1][#Branch1][N][=C][Ring1][O][N]\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" grip\\n\",\n        \"output\": \" grip is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][#Branch2][N][C][Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNCC[C@H](Oc1cccc2ccccc12)c3cccs3\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" bamboo\\n\",\n        \"output\": \" bamboo is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (3r)-n-methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H8Cl2N4O3/c1-18-6-3-7(19-2)15-10(14-6)16-9(17)8(12)5(11)4-13-16/h3-4H,1-2H3\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][C][Ring1][=C]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" FC(F)(F)c1nnc2ccc(nn12)N3CCCCC3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(4-fluorophenyl)-(6-oxo-1h-pyridin-3-yl)methyl]-2-[1-[[1-[4-(trifluoromethyl)phenyl]pyrrol-3-yl]methyl]piperidin-4-yl]acetamide\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2c(Nc3ncc(NC(=O)c4ccccc4)cn3)ncnc2cc1OCCCN5CCOCC5\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(COC(Cn2ccnc2)c3ccc(Cl)cc3Cl)cc1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-cyclohexyl-1-[(2,4-dimethoxyphenyl)methyl]-2-methyl-5-oxopyrrolidine-2-carboxamide\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-methylphenyl)acetamide\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCc1ccc(CCNCCCSCCNC[C@H](O)c2ccc(O)c3NC(=O)Sc23)cc1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" author\\n\",\n        \"output\": \" author is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-dimethylamino-3-[4-[[6-[(4-methoxyphenyl)amino]pyrimidin-4-yl]amino]phenoxy]propan-2-ol\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNc1nc2ccccc2n1Cc3sc4N(CC(C)C)C(=O)N(C)C(=O)c4c3C(=O)N5C[C@H](O)CO5\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][#C][N]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC4CCN(CC(=O)N)CC4\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" cause\\n\",\n        \"output\": \" cause is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]-(4-methyl-1,4-diazepan-1-yl)methanone\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring2][O][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][S][Cl]\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H26N2O3S/c1-3-23(19-12-6-4-7-13-19)29-27(30)25-21-16-10-11-17-24(21)28-26(20-14-8-5-9-15-20)22(25)18-33(2,31)32/h4-17,23H,3,18H2,1-2H3,(H,29,30)/t23-/m0/s1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-hydroxy-2-(4-hydroxyphenyl)chroman-4-one\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H41N3O5S/c1-19-16-23(32-5)17-20(2)25(19)34(30,31)27(4)14-15-33-18-24(29)28-12-8-22(9-13-28)21-6-10-26(3)11-7-21/h16-17,21-22H,6-15,18H2,1-5H3\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H13NO2/c17-15(18)9-10-16-13-7-3-1-5-11(13)12-6-2-4-8-14(12)16/h1-8H,9-10H2,(H,17,18)\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-tert-butyl-3-[3-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]phenyl]urea\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccc(cc1)N2C(=O)c3ccc(O)cc3C2=O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H24N2O5/c20-19(23)14-26-18-8-6-17(7-9-18)24-11-10-21-12-15(22)13-25-16-4-2-1-3-5-16/h1-9,15,21-22H,10-14H2,(H2,20,23)\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[[(3r)-3-methyl-4-[4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenyl]sulfonylpiperazin-1-yl]methyl]cyclopropane-1-carboxamide\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(Nc2ccccc2C(=O)O)cc1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H24ClN3O/c18-15-8-4-5-9-16(15)20-10-12-21(13-11-20)17(22)19-14-6-2-1-3-7-14/h4-5,8-9,14H,1-3,6-7,10-13H2,(H,19,22)\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][O][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-chloro-n-[1-[3-hydroxy-2-(hydroxymethyl)propyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][N][N][=C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H21FN4O/c23-18-12-15(14-27-10-3-11-27)13-25-21(18)16-6-8-17(9-7-16)22(28)26-20-5-2-1-4-19(20)24/h1-2,4-9,12-13H,3,10-11,14,24H2,(H,26,28)\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOc1ccc(cc1)c2cnc3CCCn23\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H25N5O4/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14/h10-11,14H,3-9H2,1-2H3,(H2,20,21,22)\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H6N2/c1-3-7-8(9-5-1)4-2-6-10-7/h1-6H\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][C][=C][Ring1][#Branch1][O][C][\\\\C][=C][\\\\C][=C][C][=C][Branch1][C][F][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][N][=C][Branch1][Ring2][C][=Ring1][Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=C(C(=O)Oc2cc(O)ccc12)c3ccc(O)cc3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H10F3N3O4/c1-11(2)9(19)17(10(20)16-11)6-3-4-8(18(21)22)7(5-6)12(13,14)15/h3-5H,1-2H3,(H,16,20)\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(N)C(=O)Nc1c(C)cccc1C\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H14N2O2S/c14-18(16,17)13-8-6-12(7-9-13)15-10-11-4-2-1-3-5-11/h1-9,15H,10H2,(H2,14,16,17)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(Cc1cccc(CC(=O)NCc2cccc(c2)c3ccc(O)cc3)c1)NC[C@H](O)c4ccc(O)c(NS(=O)(=O)C)c4\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][Branch1][C][F][O][C][=C][C][=C][Branch1][N][C][=C][Ring1][=Branch1][O][C][C][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][C][=C][Branch1][C][Cl][C][=N][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(3,4-dichlorophenyl)-n-methyl-n-(1-phenyl-2-pyrrolidin-1-ylethyl)acetamide\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-naphthalen-1-ylethoxy)ethylsulfanyl]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" channel\\n\",\n        \"output\": \" channel is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][Branch2][Ring2][=N][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][C][Branch1][=C][C][=N][N][Ring1][Branch1][C][C][=C][S][C][=N][Ring1][Branch1][=C][Ring1][#C][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(1-phenylethyl)-3h-isoindol-1-one\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H16FNO7/c1-28-21(27)19-16(24)5-2-6-17(19)29-9-3-4-12-7-8-14(22)13(10-12)18-11-15(20(25)26)23-30-18/h2-8,10-11,24H,9H2,1H3,(H,25,26)/b4-3+\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-n-[1-(2-dimethylamino-2-oxoethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H20N4O/c1-4-12-19-13-14(20(12)9-16(2,3)21)10-7-5-6-8-11(10)18-15(13)17/h5-8,21H,4,9H2,1-3H3,(H2,17,18)\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)C)C=O\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2ncc(F)c(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2n1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)C=C(CCc2ccccc2)N=C1N\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[[2-amino-5-[(2,3-difluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]-2-methylpropane-1,3-diol\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H11NO3/c17-14-12-7-6-11(8-13(12)15(18)16-14)19-9-10-4-2-1-3-5-10/h1-8H,9H2,(H,16,17,18)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2cc(ccc2c1)C(C)C(=O)O\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H18N4O3/c1-19-10-5-8(6-11(20-2)12(10)21-3)4-9-7-17-14(16)18-13(9)15/h5-7H,4H2,1-3H3,(H4,15,16,17,18)\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)O\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-oxo-6-phenyl-3-(pyridin-3-ylmethylcarbamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=N][C][S][C][=C][Branch1][Branch2][C][=C][C][=C][S][Ring1][Branch1][C][Ring1][=C][=Ring1][#Branch2]\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1r,2s)-2-methylamino-1-phenylpropan-1-ol\\n\",\n        \"output\": \" -1.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][C][N][C@@H1][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][Branch1][C][C][C@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@H1][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][Ring2][Ring2][=Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H19ClN2S/c1-19(2)10-5-11-20-14-6-3-4-7-16(14)21-17-9-8-13(18)12-15(17)20/h3-4,6-9,12H,5,10-11H2,1-2H3\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccc(cc1)C2=CC(=O)c3ccc(O)cc3O2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC=O)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(carbamoylamino)-5-[4-(2-piperidin-1-ylethoxy)phenyl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][S][C][=Ring1][Branch1][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C]\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9N3OS/c1-11-10(14)9-8(12-13-15-9)7-5-3-2-4-6-7/h2-6H,1H3,(H,11,14)\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H16ClN3O/c24-18-10-12-19(13-11-18)27-23(28)22-21(25-27)20-9-5-4-8-17(20)15-26(22)14-16-6-2-1-3-7-16/h1-13,15H,14H2\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch2][Ring1][=C][C][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H18N4O/c1-2-11-20-18(23)17-15(19)14-10-6-9-13(16(14)21-22-17)12-7-4-3-5-8-12/h3-10H,2,11H2,1H3,(H2,19,21)(H,20,23)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1onc(CO)c1C(=O)Nc2nccs2\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc2[nH]c(cc2c1)C(=O)N3CCNCC3\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H12N4O2S/c1-8-6-7-13-11(14-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15)\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][Branch1][P][N][C][C][O][C@@H1][Branch1][#Branch1][C][N][Branch1][C][C][C][C][Ring1][#Branch2][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=Branch1][S][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring2][Ring1][=Branch2][=Ring1][#Branch2][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)(O)c1ccccc1CC[C@@H](SCC2(CC(=O)O)CC2)c3cccc(\\\\C=C\\\\c4ccc5ccc(Cl)cc5n4)c3\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(CNc2nc(nc3ncccc23)N4CCN(CC4)C(=O)[C@H]5CCCCN5)c(Cl)c1\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H25N7O2/c1-17(26(34)32(2)3)35-23-9-6-8-21-24(23)25(29-16-28-21)31-19-10-11-22-18(13-19)14-30-33(22)15-20-7-4-5-12-27-20/h4-14,16-17H,15H2,1-3H3,(H,28,29,31)/t17-/m1/s1\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2OC(=O)Nc2c1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc2nc(NCCN)c3ncc(C)n3c2c1\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H6N2O/c11-8-4-5-9-7-3-1-2-6-10(7)8/h1-6H\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(ccc1Cn2ccc3ccc(cc23)C(=O)NCC4CCCC4)C(=O)NS(=O)(=O)c5ccccc5\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4cocc4)C3=O\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1cc(nc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C@H1][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring1][P][=O]\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[1-(4-aminophenyl)cyclohexyl]aniline\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 9-(2-morpholin-4-ylethyl)-2,4-dipyrrolidin-1-yl-5,6,7,8-tetrahydropyrimido[6,5-b]indole\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=Branch2][Ring1][Ring2][=C][C][=C][Ring1][=Branch1][C][=C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Ring1][Branch2][N][C][C@H1][Branch1][#Branch2][C][N][N][=N][C][=C][Ring1][Branch1][F][O][C][Ring1][N][=O]\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-chloro-1-(2-diethylaminoethyl)-5-(2-fluorophenyl)-3h-1,4-benzodiazepin-2-one\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc2c3ccccc3C(=O)C(=O)c2c1\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][Ring2][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-[3-(trifluoromethyl)phenyl]sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H23NO/c1-3-15(9-4-5-10-16(2)12-15)13-7-6-8-14(17)11-13/h6-8,11,17H,3-5,9-10,12H2,1-2H3\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][N][C][Branch1][C][N][=N][C][Ring1][#Branch1][=N][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-methoxy-n-propan-2-yl-2-pyridin-2-ylpyrimidin-4-amine\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-phenylaniline\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(2s)-3-methyl-1-oxo-1-pyrrolidin-1-ylbutan-2-yl]-3-phenylpropanamide\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1cc2c(NC(NS2(=O)=O)C(Cl)Cl)cc1Cl\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)N(c1ccc(C(=O)N)c(n1)c2ccc(F)cc2F)c3c(F)cccc3F\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCCNCCNc1ccc2c(NC(=O)CC34CC5CC(CC(C5)C3)C4)cccc2n1\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H12N2O2/c16-15(19)17-12-7-3-1-5-10(12)9-14(18)11-6-2-4-8-13(11)17/h1-8H,9H2,(H2,16,19)\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(cc(OC)c1OC)C(=O)N2CC[C@@](CCN3CCC(CC3)(C(=O)N)c4ccccc4)(C2)c5ccc(Cl)c(Cl)c5\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-methyl-3h-imidazole-2-thione\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)Cc3ccc(cc3)C(=O)O)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][Branch1][C][C][C][C][O][C][=Branch1][C][=O][C][=Ring1][=Branch1][C][Branch1][C][O][=C][Ring1][N][C][\\\\C][=C][Branch1][C][/C][\\\\C][C][C][=Branch1][C][=O][O][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)C(=O)N2CCCC2=O\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H28N2O3/c1-13(20-9-14-6-15(10-20)8-16(7-14)11-20)21-12-19(23)17-2-4-18(5-3-17)22(24)25/h2-5,13-16,19,21,23H,6-12H2,1H3\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-acetamido-3-(4-chlorophenoxy)-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" -1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=C][C][Branch2][Ring1][S][C][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][C][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][O][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)CCOc1ccc(cc1)C(O)(Cc2ccc(Cl)cc2)c3ccc(C)cc3\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-phenylbutyl)benzamide\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H7NO/c11-9-6-5-7-3-1-2-4-8(7)10-9/h1-6H,(H,10,11)\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=N][C][=Branch1][#Branch1][=N][N][Ring1][=C][Ring1][Branch1][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1OCC(O)CO\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC1=CC2=NNC(=O)N2c3cc(ccc13)c4ccc[nH]4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNC1(C)C2CCC(C2)C1(C)C\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H29Cl2N3O4S/c25-22-7-6-21(16-23(22)26)33-20-10-14-28(15-11-20)19-8-12-29(13-9-19)24(30)27-34(31,32)17-18-4-2-1-3-5-18/h1-7,16,19-20H,8-15,17H2,(H,27,30)\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16ClNO3/c17-15-11-5-6-18-8-13(9-1-3-10(19)4-2-9)12(11)7-14(20)16(15)21/h1-4,7,13,18-21H,5-6,8H2\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[[1-[2-[3-oxo-6-(trifluoromethoxy)-1,4-benzoxazin-4-yl]ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1CCC[C@H]1CNC(=O)c2cc(ccc2OC)S(=O)(=O)N\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][N][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H33N3O4S2/c1-2-31-18-6-4-17(5-7-18)10-12-25-11-3-14-32-15-13-26-16-21(29)19-8-9-20(28)22-23(19)33-24(30)27-22/h4-9,21,25-26,28-29H,2-3,10-16H2,1H3,(H,27,30)/t21-/m0/s1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCNCc1cnc(s1)c2ccc(cc2)C(=O)Nc3ccccc3N\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Branch2][C][C][N][Branch1][C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=S(=O)(Nc1ccccc1c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(N(O)C(=O)N)c1cc2ccccc2s1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1[nH]c(C(=O)NC2CCN(CC2)c3nc(cs3)C(=O)O)c(Cl)c1Cl\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2-hydroxyphenyl) naphthalene-1-carboxylate\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(N1NC(=O)C2=C(C1=O)C(=O)c3ccc(Cl)cc3N2)c4oc5ccccc5c4\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cnc(nc1N2CCOCC2)c3ccccn3\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-chloro-n-[1-[(2r)-2,3-dihydroxypropyl]-2-oxo-3,4-dihydroquinolin-3-yl]-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-piperidin-3-yl-1,3-benzothiazole\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@][C][C][C][=Branch1][C][=O][C][=C][Ring1][#Branch1][C][=C][C@@H1][C@@H1][Ring1][O][C][C][C@@][Branch1][C][C][C@H1][Ring1][#Branch1][C][C][C@@][Ring1][=Branch1][C][C][C][=Branch1][C][=O][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n-dimethyl-3-[2-(trifluoromethyl)phenothiazin-10-yl]propan-1-amine\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(4-aminophenyl)-1,3-benzothiazol-6-ol\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H23N3O/c1-19(2)12-13-20(17-6-4-5-11-18-17)14-15-7-9-16(21-3)10-8-15/h4-11H,12-14H2,1-3H3\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H24FNO4/c26-17-9-7-15(8-10-17)24-20-3-1-2-4-22(20)27-25(16-5-6-16)21(24)12-11-18(28)13-19(29)14-23(30)31/h1-4,7-12,16,18-19,28-29H,5-6,13-14H2,(H,30,31)/b12-11+/t18-,19-/m1/s1\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-[2-(3,5-dimethylphenyl)-1h-indol-3-yl]ethyl]-4-pyridin-4-ylbutan-1-amine\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccccc1Nc2ncnc3ccccc23\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring2][Ring2][N][C][=Branch1][C][=O][C][=C][Branch1][C][N][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)CCNC(=O)c1c(C)[nH]c(\\\\C=C\\\\2/C(=O)Nc3ccc(F)cc23)c1C\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20N2O2S/c1-14-15(4-2-6-18(14)20)13-21-9-7-16(12-19(21)22)23-10-8-17-5-3-11-24-17/h2-7,9,11-12H,8,10,13,20H2,1H3\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)CCOc1ccc(cc1OC)N(C)C(=O)c2ccc(cc2)c3ccc(cc3)C(F)(F)F\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(3-morpholin-4-ylsulfonylphenyl)imidazo[1,2-a]pyrimidine\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][S][C][=N][C][=C][C][=C][Branch1][=N][N][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][O][C][=C][Ring1][=C][S][Ring1][P]\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" grouse\\n\",\n        \"output\": \" grouse is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(CCOc1ccc(C[C@H](Nc2ccccc2C(=O)c3ccccc3)C(=O)O)cc1)c4ccccn4\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)c2nn(c3ncnc(N)c23)C(C)(C)C\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H7BrO/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6,12H\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=N+1][Branch1][C][O-1][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[(3s)-3-(4-methylsulfonylphenyl)-3-phenylpropyl]piperidin-4-yl]acetamide\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14N2O4/c1-7(2)8-3-4-12-9(5-8)13(19)10-6-11(16(20)21)14(17)18-15(10)22-12/h3-7H,1-2H3,(H2,17,18)(H,20,21)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H22ClFN4O2/c1-28-19-9-15-18(10-20(19)29-11-13-4-6-24-7-5-13)25-12-26-21(15)27-17-3-2-14(22)8-16(17)23/h2-3,8-10,12-13,24H,4-7,11H2,1H3,(H,25,26,27)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[(e)-2-[5-methylsulfanyl-2-(phenylmethoxy)phenyl]ethenyl]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H18N2OS/c1-11(17)7-12-9-18-16-5-4-13(8-15(12)16)19-10-14-3-2-6-20-14/h2-6,8-9,11,18H,7,10,17H2,1H3\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)CCCC(C)Nc1c2ccc(Cl)cc2nc3ccc(OC)cc13\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27ClN4O3/c1-28-8-6-15(7-9-28)13-31-22-12-19-17(11-21(22)30-3)23(26-14-25-19)27-20-10-16(29-2)4-5-18(20)24/h4-5,10-12,14-15H,6-9,13H2,1-3H3,(H,25,26,27)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)N1CCC[C@@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2,6-dimethylpyridin-4-yl)methyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamate\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3,5-dichloropyridin-4-yl)-8-methoxyquinoline-5-carboxamide\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" forgery\\n\",\n        \"output\": \" forgery is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H12F2N6O/c14-10-1-2-11(12(15)3-10)13(22,4-20-8-16-6-18-20)5-21-9-17-7-19-21/h1-3,6-9,22H,4-5H2\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H12N2/c9-10-7-6-8-4-2-1-3-5-8/h1-5,10H,6-7,9H2\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H21ClF3NO4S/c1-15(21-11-7-18(26)13-16(21)3-2-4-24(30)31)29(23-14-19(27)8-12-22(23)28)34(32,33)20-9-5-17(25)6-10-20/h5-15H,2-4H2,1H3,(H,30,31)/t15-/m1/s1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][P][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][Ring1][#C][C][Ring2][Ring1][Ring1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(3-chlorophenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (5r)-3-[4-(1,1-dioxo-3,6-dihydro-2h-thiopyran-4-yl)-3-fluorophenyl]-5-[(4-methyltriazol-1-yl)methyl]-1,3-oxazolidin-2-one\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)CCc1oc(c2ccccc2)c(n1)c3ccccc3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCc1ccc(NC(=O)c2ccc3cc(ccc3c2)C(=N)N)cc1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H14N4O/c1-16-8-4-2-7(3-5-8)6-9-10(12)14-15-11(9)13/h2-5H,6H2,1H3,(H5,12,13,14,15)\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][S][C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5,6-dimethoxy-2-[[1-(phenylmethyl)piperidin-4-yl]methyl]-2,3-dihydroinden-1-one\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H14N2O2S/c11-9-3-5-10(6-4-9)15(13,14)12-7-1-2-8-12/h3-6H,1-2,7-8,11H2\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" sheep\\n\",\n        \"output\": \" sheep is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H16ClNO3S2/c1-3-7(2)8(6-13)12-17(14,15)10-5-4-9(11)16-10/h4-5,7-8,12-13H,3,6H2,1-2H3/t7-,8+/m0/s1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(2-methoxyphenoxy)propane-1,2-diol\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C@@H1][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C@@H1][Branch1][Ring1][C][O][N][C][Ring1][#C][=O]\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[3-(2-methylpropoxy)-2-pyrrolidin-1-ylpropyl]-n-(phenylmethyl)aniline\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2][C][C][=C]\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n',n'-dimethyl-n-(phenylmethyl)-n-pyridin-2-ylethane-1,2-diamine\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C@H1][Branch2][Ring2][Ring1][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][C][C][=O]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H18FN3O3/c18-13-7-11-14(8-15(13)20-5-3-19-4-6-20)21(10-1-2-10)9-12(16(11)22)17(23)24/h7-10,19H,1-6H2,(H,23,24)\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][Ring1][O][C][=N][C][=Branch1][Ring2][=N][Ring1][Branch2][N][N][=C][C][=Branch1][=Branch2][=C][Branch1][C][Cl][C][Ring1][#Branch1][=O][Cl]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1nnc(N)s1\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H25N3O/c1-17(24)21-15-18-7-9-19(10-8-18)16-22-11-13-23(14-12-22)20-5-3-2-4-6-20/h2-10H,11-16H2,1H3,(H,21,24)\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [5-amino-1-(4-fluorophenyl)pyrazol-4-yl]-[3-[(2s)-2,3-dihydroxypropoxy]phenyl]methanone\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[2,6-difluoro-4-[(5r)-5-(1,2-oxazol-3-yloxymethyl)-2-oxo-1,3-oxazolidin-3-yl]phenyl]-3,6-dihydro-2h-pyridine-1-carbaldehyde\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" computer\\n\",\n        \"output\": \" computer is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H25N3O3/c1-16-8-11-19(25-24(29)18-6-5-7-20(14-18)27(2)3)15-22(16)26-23(28)17-9-12-21(30-4)13-10-17/h5-15H,1-4H3,(H,25,29)(H,26,28)\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H17FN8/c1-8-5-19-15(20-10(3)14-17-6-11(16)7-18-14)22-13(8)21-12-4-9(2)23-24-12/h4-7,10H,1-3H3,(H3,19,20,21,22,23,24)/t10-/m0/s1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H29F2N3O3/c27-21-13-20(14-22(28)15-21)23-16-26(34-29-23)31(11-5-10-30-8-3-1-2-4-9-30)17-19-6-7-24-25(12-19)33-18-32-24/h6-7,12-16H,1-5,8-11,17-18H2\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H28N2O6/c1-17(11-19-7-5-4-6-8-19)33-22-12-21(13-23(14-22)34-18(2)16-32-3)25(29)28-24-10-9-20(15-27-24)26(30)31/h4-10,12-15,17-18H,11,16H2,1-3H3,(H,30,31)(H,27,28,29)/t17-,18-/m0/s1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCN4CCCC4\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][N][Branch1][#Branch1][C][C][Ring1][=N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch1][#Branch2][C][C][N][C][C][C][C][Ring1][Branch1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H9NO2/c15-11-7-3-6-10-12(11)8-4-1-2-5-9(8)13(16)14(10)17/h1-7H,15H2\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-3-chloro-2-(piperidin-4-ylmethylamino)pyridine-4-carboxamide\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(z)-(5-chloro-2-oxo-1h-indol-3-ylidene)methyl]-n-(2-diethylaminoethyl)-2,4-dimethyl-1h-pyrrole-3-carboxamide\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H8N2/c10-8-3-4-9-7(6-8)2-1-5-11-9/h1-6H,10H2\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][#C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@@H1][Branch1][Ring1][C][O][O][C][=C][C][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][Ring2][=C][Ring1][P][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][=N][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][Ring1][#Branch2][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][=N][NH1][N][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-(6-amino-3-azabicyclo[3.1.0]hexan-3-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][C@@H1][C][N][Branch1][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][C][C@H1][Ring1][=C][C][C][NH1][C][=C][C][=C][Branch1][O][C][=C][Ring1][=Branch1][C][Ring2][Ring1][=Branch2][=Ring1][=Branch2][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][C][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][S][C][C][C][N][Branch2][Ring2][Ring2][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCSc1ccc(cc1)c2cc(ccc2OCC(=O)O)C(F)(F)F\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1-adamantylmethyl)-5-chloro-2-piperazin-1-ylpyridine-4-carboxamide\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11N3O2S/c13-11(16)10-8(15-12(14)17)6-9(18-10)7-4-2-1-3-5-7/h1-6H,(H2,13,16)(H3,14,15,17)\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNC(=O)c1ccc(C)c(c1)N2C(=CC(=C(Br)C2=O)OCc3ccc(F)cc3F)C\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[2-oxo-2-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]amino]ethyl]benzoic acid\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(6-bicyclo[2.2.1]hept-2-enyl)-6-chloro-1,1-dioxo-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][N][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1[nH]c(\\\\C=C\\\\2/C(=O)Nc3ccc(F)cc23)c(C)c1C(=O)NC[C@H](O)CN4CCOCC4\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2c(Nc3c(Cl)ccc4OCOc34)ncnc2cc1OCCCN5CCCCC5\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H17N3O/c1-16-6-8-17(9-7-16)14(18)13-10-11-4-2-3-5-12(11)15-13/h2-5,10,15H,6-9H2,1H3\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][#C][C][=Branch1][C][=O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][Ring2][Ring1][Ring2][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[2-[3-(trifluoromethyl)phenyl]ethylamino]propylsulfanyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H16ClFN6O2/c1-28-17-7-13-16(8-18(17)29-5-4-27-11-22-9-25-27)23-10-24-19(13)26-15-3-2-12(20)6-14(15)21/h2-3,6-11H,4-5H2,1H3,(H,23,24,26)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-2-amino-n-[(2r)-1-(4-butanoyl-4-phenylpiperidin-1-yl)-3-(4-methoxyphenyl)-1-oxopropan-2-yl]-3-(3-methylimidazol-4-yl)propanamide\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H21ClFN5O2/c1-30-18-9-16-13(8-12(18)10-28-7-3-6-17(28)20(24)29)21(26-11-25-16)27-15-5-2-4-14(22)19(15)23/h2,4-5,8-9,11,17H,3,6-7,10H2,1H3,(H2,24,29)(H,25,26,27)/t17-/m1/s1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H12N2O5S/c18-14-13-10(5-6-23-13)16(15(19)17(14)20)7-9-8-21-11-3-1-2-4-12(11)22-9/h1-6,9,20H,7-8H2\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][C][O][C][=N][C][Branch1][C][N][=C][N][C][=Branch1][C][=O][N][Branch2][Ring1][Ring1][C][C][=C][C][=C][C][Branch1][Branch2][C][C][=Branch1][C][=O][O][C][=C][Ring1][O][C][Ring2][Ring1][C][=N][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch2][Ring1][O][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1][C][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(3,4-difluorophenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][S][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1(C)C(=O)Nc2ccccc12\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (3r,5r)-7-[(1s,2s,6r,8s,8ar)-8-(2,2-dimethylbutanoyloxy)-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 9-amino-3,3-dimethyl-2,4-dihydroacridin-1-one\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H21N3O2S/c1-16(2)14(19)17-7-5-11(6-8-17)13(18)15-10-12-4-3-9-20-12/h3-4,9,11H,5-8,10H2,1-2H3,(H,15,18)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-[4-(3-chlorophenyl)piperazin-1-yl]propyl]-[1,2,4]triazolo[4,5-a]pyridin-3-one\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H24ClN3O3/c24-17-6-7-19-16(13-17)14-20(25-19)22(29)26-21(12-15-4-2-1-3-5-15)23(30)27-10-8-18(28)9-11-27/h1-7,13-14,18,21,25,28H,8-12H2,(H,26,29)/t21-/m0/s1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H17ClN2O2/c1-12-6-7-18-16(10-12)20(13(2)24(18)11-19(25)26)14-8-9-23-21-15(14)4-3-5-17(21)22/h3-10H,11H2,1-2H3,(H,25,26)\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-[(3-chloro-2-methylphenyl)sulfonylamino]-1,3-thiazol-4-yl]-n,n-diethylacetamide\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H26FN3O5/c1-23(2)9-13-10-24(6-7-30-13)18-16(22)8-14-17(20(18)29-3)25(12-4-5-12)11-15(19(14)26)21(27)28/h8,11-13H,4-7,9-10H2,1-3H3,(H,27,28)/t13-/m0/s1\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H24N2OS/c1-14(12-20(2)3)13-21-16-7-5-6-8-18(16)23-19-10-9-15(22-4)11-17(19)21/h5-11,14H,12-13H2,1-4H3/t14-/m1/s1\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzenesulfonamide\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(CO)Nc1nc(SCc2cccc(F)c2F)nc3nc(N)sc13\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3c[nH]c4ccccc34)c2C(=O)N5CC[C@@H](O)C5\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)-n-(2-ethylhexyl)benzamide\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1nc(N)n(n1)c2ccccc2\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2cc(ccc2c1)[C@H](C)C(=O)O\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H26F3N5O5/c1-16(2)22(23(36)26(27,28)29)32-21(35)15-34-20(18-8-4-3-5-9-18)11-10-19(24(34)37)31-25(38)30-13-17-7-6-12-33(39)14-17/h3-12,14,16,22H,13,15H2,1-2H3,(H,32,35)(H2,30,31,38)\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C@@H1][C][C][C][N][Branch1][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H8N4/c1-2-4-11-10(3-1)13-14-15(11)9-5-7-12-8-6-9/h1-8H\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1][Ring1][S]\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[3-(dimethylcarbamoyl)phenyl]sulfonyl-4-[(3-methoxyphenyl)amino]-8-methylquinoline-3-carboxamide\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[(e)-2-(4-chlorophenyl)ethenyl]pyrimidin-2-amine\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=N][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H11ClN4O3/c18-10-1-2-11-12(7-10)20-14-13(15(11)23)17(25)22(21-16(14)24)8-9-3-5-19-6-4-9/h1-7H,8H2,(H,20,23)(H,21,24)\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCC(CO)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)Cc1ccc(cc1)C(C)C(=O)NS(=O)(=O)C\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@H1][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring2][#Branch2][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][#C][Cl]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][Branch2][Ring1][#Branch2][C][C][C][O][C][=C][Branch1][C][Cl][C][=C][Branch1][=Branch1][C][=C][Ring1][#Branch1][Cl][C][=N][C][C][O][Ring1][Branch1][O][N][=Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-chloro-n-[(2s,3r)-4-[(3s,4r)-3,4-dihydroxypyrrolidin-1-yl]-3-hydroxy-4-oxo-1-phenylbutan-2-yl]-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)N4CCN(CC4)C(=O)C)n2\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1(CNC(=O)c2cc(ccc2Cl)N3N=CC(=O)NC3=O)CCCCCC1\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCC(COc2cc(OC3CCOCC3)c4c(Nc5c(Cl)ccc6OCOc56)ncnc4c2)CC1\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][C][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch2][Ring1][Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1CN(CCN1Cc2cc(Cl)ccc2OCC(=O)O)S(=O)(=O)c3ccccc3\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H28FNO3/c1-26-20-5-3-4-19(22(20)27-2)21(25)17-11-14-24(15-12-17)13-10-16-6-8-18(23)9-7-16/h3-9,17,21,25H,10-15H2,1-2H3/t21-/m1/s1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-amino-4-dimethylamino-n-(phenylmethyl)thieno[5,4-b]pyridine-2-carboxamide\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(4-chlorophenyl)-1-(1h-indol-3-ylmethyl)piperidin-4-ol\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" FC(F)(F)Oc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1ccc(O)cc1\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(N1C(=O)c2ccccc2C1=O)C(=O)N3CCc4ccccc4C3\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][S+1][Branch1][C][O-1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-1-naphthalen-1-yloxy-3-(propan-2-ylamino)propan-2-ol\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H23N3O3/c1-15-7-10-18(24-23(29)17-5-4-6-19(13-17)26(2)3)14-21(15)25-22(28)16-8-11-20(27)12-9-16/h4-14,27H,1-3H3,(H,24,29)(H,25,28)\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H19NO/c1-2-6-14(7-3-1)17-15-8-4-5-9-16(15)18(20-17)10-12-19-13-11-18/h1-9,17,19H,10-13H2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-chloro-1h-indazole\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H27NO2/c1-13-17(4-3-5-18(13)23-2)21-19(22)12-20-9-14-6-15(10-20)8-16(7-14)11-20/h3-5,14-16H,6-12H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1CCN(CC1)C(=O)c2cc3cc(F)ccc3[nH]2\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][Branch2][Ring2][#Branch1][C][=Branch1][C][=O][N][C@@H1][Branch2][Ring1][=Branch2][C][C][=C][C][=C][Branch1][=C][O][C][C][C][N][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring1][P][C][=Branch1][C][=O][O][C][Branch1][C][C][=C][Ring2][Ring1][P]\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H12O4/c16-10-3-1-9(2-4-10)14-8-13(18)12-6-5-11(17)7-15(12)19-14/h1-7,14,16-17H,8H2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)N2Sc3ccccc3C2=O\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1(COc2ccc3c(c2)ncn3c4ccc5cccc(N6CCC(N)CC6)c5n4)COC1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (4r)-2-(3,4-dimethoxy-5-propylphenyl)-n-hydroxy-4,5-dihydro-1,3-oxazole-4-carboxamide\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H22N2/c19-16-8-4-14(5-9-16)18(12-2-1-3-13-18)15-6-10-17(20)11-7-15/h4-11H,1-3,12-13,19-20H2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H31NO7/c1-15(5-7-19(25)30-13-10-24-8-11-29-12-9-24)4-6-17-21(26)20-18(14-31-23(20)27)16(2)22(17)28-3/h4,26H,5-14H2,1-3H3/b15-4+\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H18N2O5/c1-28-21(25)19(13-14-9-11-16(12-10-14)23(26)27)22-20(24)18-8-4-6-15-5-2-3-7-17(15)18/h2-12,19H,13H2,1H3,(H,22,24)/t19-/m0/s1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)c2ccc(cc2)C3(O)CN4CCC3CC4\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H27FN2O5/c1-15(27)25-20-4-3-18(28)11-22(20)30-14-19(29)13-26-8-6-23(7-9-26)12-16-10-17(24)2-5-21(16)31-23/h2-5,10-11,19,28-29H,6-9,12-14H2,1H3,(H,25,27)/t19-/m0/s1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H29N7O4/c1-36-23-14-21-22(15-24(23)38-11-5-8-34-9-12-37-13-10-34)30-18-31-25(21)33-27-28-16-20(17-29-27)32-26(35)19-6-3-2-4-7-19/h2-4,6-7,14-18H,5,8-13H2,1H3,(H,32,35)(H,28,29,30,31,33)\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][N][=N][C][=C][Branch1][#Branch2][N][=C][N][Ring1][Branch1][C][Ring1][=Branch2][=O][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C[C@H](N)c1oc(nn1)S(=O)(=O)Cc2ccc(F)cc2\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][C][N][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H15NO2/c1-8-7-12(16)17-14-10-4-3-5-15-13(10)9(2)6-11(8)14/h6-7,15H,3-5H2,1-2H3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C29H30N4O5S/c1-38-27-16-21(29(35)32-39(36,37)24-9-3-2-4-10-24)11-12-22(27)18-33-19-30-25-14-13-23(17-26(25)33)31-28(34)15-20-7-5-6-8-20/h2-4,9-14,16-17,19-20H,5-8,15,18H2,1H3,(H,31,34)(H,32,35)\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H11BrN2O/c15-10-7-5-9(6-8-10)13-16-12-4-2-1-3-11(12)14(18)17-13/h1-8,13,16H,(H,17,18)\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-phenylethoxy)ethylsulfanyl]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][=C][Ring1][=Branch1][C][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1)c2ncn(C3CCNCC3)c2c4ccncc4\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H9NO2/c15-8-5-6-10-9-3-1-2-4-11(9)13(16)14(17)12(10)7-8/h1-7H,15H2\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][C][S][C][=Branch1][Branch2][=N][C][=Ring1][Branch1][C][Ring1][N][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(Nc1nc2C(=O)NC=Nc2s1)c3ccccc3\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-phenyl-2,3,4,5-tetrahydro-3-benzazepin-1-ol\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][O][N][C][=N][N][=C][Branch1][#Branch2][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[[6-[(2,5-dichlorophenyl)amino]pyrimidin-4-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=N][C][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H11BrN2O2S/c1-7-6-10(19)18-15-11(7)12(17)14(21-15)13(20)8-2-4-9(16)5-3-8/h2-6H,17H2,1H3,(H,18,19)\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" fact\\n\",\n        \"output\": \" fact is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 8-nitro-2-(trichloromethyl)quinoline\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccccc1C(=O)N2CCN(CC2)c3ccccn3\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][=Branch2][N][C][=N][C][=Branch1][C][=O][C@@][Branch1][C][C][Branch1][Ring2][S][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1ccc(Br)cc1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][C][N][C][C][C][O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H25NO4/c1-17-21(26)19-11-8-12-20(23(19)29-22(17)18-9-4-2-5-10-18)24(27)28-16-15-25-13-6-3-7-14-25/h2,4-5,8-12H,3,6-7,13-16H2,1H3\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H18N2O3/c1-13(22-19(24)16-8-4-5-9-17(16)20(22)25)18(23)21-11-10-14-6-2-3-7-15(14)12-21/h2-9,13H,10-12H2,1H3\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H18N2OS/c17-15-14(12-8-4-5-9-13(12)20-15)16(19)18-10-11-6-2-1-3-7-11/h1-3,6-7H,4-5,8-10,17H2,(H,18,19)\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-methyl-1,2-di(pyridin-3-yl)propan-1-one\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1C2CCC(N2)C(=O)N1Cc3ccccc3\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-n-(2-hydroxyphenyl)-5-nitrobenzamide\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=C][Branch1][C][O][C][=Branch2][Ring1][#Branch2][=C][C][=C][Ring1][#Branch1][O][C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][C][Br][=C][Ring1][#Branch2][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n2,n2,n4,n4,n6,n6-hexamethyl-1,3,5-triazine-2,4,6-triamine\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-bromophenyl)sulfonyl-n-(5-chloro-2-methoxyphenyl)propanamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H8N6OS/c1-6-2-3-11-9-13-7(15-16(6)9)8(17)14-10-12-4-5-18-10/h2-5H,1H3,(H,12,14,17)\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n'-[(3-pyridin-3-ylphenyl)methyl]pyridine-2,3-diamine\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 9-chloro-2-furan-2-yl-[1,2,4]triazolo[1,5-c]quinazolin-5-amine\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[S+]([O-])c1ccc(cc1)c2nc(c3ccc(F)cc3)c([nH]2)c4ccncc4\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[6-(cyclopentyloxycarbonylamino)indol-1-yl]methyl]-3-methoxybenzoic acid\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-2-[[5-chloro-4-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]pyrimidin-2-yl]amino]-2-(4-fluorophenyl)ethanol\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch2][Ring2][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)C)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][N][=C][Branch1][C][N][N][Branch1][Ring2][N][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H19N3O/c1-24-19-5-3-2-4-17(19)18-14-16(7-8-20(18)24)23-21(25)9-6-15-10-12-22-13-11-15/h2-5,7-8,10-14H,6,9H2,1H3,(H,23,25)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1SC(=O)c2cc(ccc12)S(=O)(=O)NC3CC3\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring1][Ring2][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][#C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H24ClN5O2/c1-27(2)13-18(28)14-29-19-9-7-17(8-10-19)25-21-23-12-11-20(26-21)24-16-5-3-15(22)4-6-16/h3-12,18,28H,13-14H2,1-2H3,(H2,23,24,25,26)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)NCC=C)C(F)(F)F\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3ccncc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)Cc1nc(cs1)c2ccccc2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][Branch1][O][\\\\C][=C][\\\\C][=C][C][=C][C][=N][Ring1][=Branch1][=N][NH1][C][Ring1][=N][=C][Ring1][P]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch2][Ring2][=N][C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=C][N][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Branch1][N][N][C][C][C][Branch1][C][N][C][C][Ring1][#Branch1][C][Ring1][=N][=N][Ring1][P][C][O][C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H17N3O4S/c19-12(3-4-13(20)21)18-7-5-10(6-8-18)15-16-14(17-22-15)11-2-1-9-23-11/h1-2,9-10H,3-8H2,(H,20,21)\\n\",\n        \"output\": \" -1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H15N3OS/c1-4-7-5(2)8-9(13)10(11(14)16)17-12(8)15-6(7)3/h4,13H2,1-3H3,(H2,14,16)\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](Nc1nc(Nc2cc(C)[nH]n2)cc(n1)N3CCOCC3)c4ncc(F)cn4\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H32O3/c1-4-20(24)25-19-8-7-17-16-6-5-14-13-15(23)9-11-21(14,2)18(16)10-12-22(17,19)3/h13,16-19H,4-12H2,1-3H3/t16-,17-,18-,19-,21-,22-/m0/s1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][C][Branch1][C][O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11N3O/c16-12-9-7-11(8-1-4-13-5-2-8)15-10(9)3-6-14-12/h1-2,4-5,7,15H,3,6H2,(H,14,16)\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-chloro-3-methyl-4h-benzo[e][1,2,4]thiadiazine 1,1-dioxide\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-phenylbenzamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)c1[nH]c2cc(Cl)cc(Cl)c2c1\\\\C=C\\\\3/CCN(C3=O)c4ccccc4\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][N][C][=N][C][Branch2][Ring1][Branch2][N][C][=C][C][=C][C][Branch1][=N][N][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=C][Ring1][=C][=N][C][=C][Ring2][Ring1][Branch1][Br]\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H17ClN2O3S/c1-11-19(26-15-6-3-13(20)4-7-15)16-9-14(21-12(2)23)5-8-17(16)22(11)10-18(24)25/h3-9H,10H2,1-2H3,(H,21,23)(H,24,25)\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H19N3O2/c18-15-3-1-2-4-16(15)19-17(21)13-5-7-14(8-6-13)20-9-11-22-12-10-20/h1-8H,9-12,18H2,(H,19,21)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)C)C(F)(F)F\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][F][C][Branch2][Ring1][S][N][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][Ring1][P][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H7N3S/c1-2-4-8-7(3-1)12-10(13-8)9-5-14-6-11-9/h1-6H,(H,12,13)\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(CNC(=O)c2sc3nc(C)cc(C)c3c2N)cc1\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C][C][N][C][=C][C][=C][C][Branch1][#C][N][C][=Branch1][C][=O][C][C][C][C][C][C][C][Ring1][=Branch1][=C][Branch1][C][Cl][C][=C][C][Ring1][P][=N][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(2-fluorophenyl)amino]-n-(3-methyl-4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccncc2)C(F)(F)F\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][S][C][=Branch1][=Branch1][=N][C][Ring1][Branch1][=O][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC1(C(=O)Nc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][C][N][Branch1][#C][C@H1][Branch1][=Branch2][C][N][C][C][C][C][Ring1][Branch1][C][Ring1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[(3,4-dichlorophenyl)methyl]-5-nitroindole-2-carboxylic acid\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H20N4O3S/c1-23-7-6-19-9-10-2-4-11(5-3-10)13-8-12(14(17)21)15(24-13)20-16(18)22/h2-5,8,19H,6-7,9H2,1H3,(H2,17,21)(H3,18,20,22)\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][P][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-methoxy-n-methyl-n-phenyl-2-pyridin-2-ylpyrimidin-4-amine\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCC1(CCC(=O)NC1=O)c2ccc(N)cc2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(dipropylsulfamoyl)benzoic acid\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-chloro-n-(4,5-dihydro-1h-imidazol-2-yl)-2,1,3-benzothiadiazol-7-amine\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)C2=CC(=O)c3ccccc3N2\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H18N2O5S/c22-18-16-11-15(8-9-17(16)20-19(18)23)27(24,25)21-10-4-5-13(21)12-26-14-6-2-1-3-7-14/h1-3,6-9,11,13H,4-5,10,12H2,(H,20,22,23)/t13-/m0/s1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1cccc2C(=O)C(=O)c3ccccc3c12\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC(=O)Nc1cc(sc1C(=O)N)c2ccccc2\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(C)c(NC(=O)CC23CC4CC(CC(C4)C2)C3)c1\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cccc(Br)c1C(=O)N[C@@H](Cc2ccc(NC(=O)c3c(Cl)cccc3Cl)cc2)C(=O)O\\n\",\n        \"output\": \" -0.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-(4-chlorophenyl)-2-pyridin-2-ylethanone\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H22N2O/c1-17(20-14-13-19(2)3,15-9-5-4-6-10-15)16-11-7-8-12-18-16/h4-12H,13-14H2,1-3H3\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(OC)c(c1)C(O)CNC(=O)CN\\n\",\n        \"output\": \" -0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-(2,4-difluorophenoxy)-2-(1,5-dihydroxypentan-3-ylamino)-8-methylpyrido[6,5-d]pyrimidin-7-one\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-bromo-n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2,6-dimethoxybenzamide\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4cccnn34)cc1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NNCCc1ccccc1\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring1][Ring1][C][C][=N][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][C][C][=Branch1][C][=O][N][C][C][C][N][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Br][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N]\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[[6-[(2-chloro-5-methylphenyl)amino]pyrimidin-4-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(9-ethylcarbazol-3-yl)acetamide\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [4-[(2r)-1-oxo-1-(2-pyrrolidin-1-ylethylamino)propan-2-yl]phenyl] trifluoromethanesulfonate\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccccc1OC(=O)c2cccc3ccccc23\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C1CN2CCC1C(=C2)c3oc4ccccc4c3\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][Branch1][N][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][N][C][=Branch1][C][=O][C][N][Branch2][Ring1][Ring1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=C][=C][Ring2][Ring1][C][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCc1cc(cc(OC)c1OC)C2=N[C@H](CO2)C(=O)NO\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H16N2S/c1-8-5-4-6-11(9(8)2)10(3)12-7-14-13(16)15-12/h4-7,10H,1-3H3,(H2,14,15,16)/t10-/m0/s1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H20N2S/c1-12-8-9-16(14(17)10-12)19-15-7-5-4-6-13(15)11-18(2)3/h4-10H,11,17H2,1-3H3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][C][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-[6-[(4-phenylphenyl)methoxy]-1,2,3,4-tetrahydronaphthalen-2-yl]ethyl]piperidine\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(2-fluorophenyl)methylsulfanyl]-7-[[(2r)-1-hydroxypropan-2-yl]amino]-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(3-cyclopropyl-1,2-oxazol-5-yl)methyl]-n'-(5-methyl-1h-pyrazol-3-yl)pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OB1N(C(=O)Nc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][=C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-2-[[2-(benzoyl)phenyl]amino]-3-[4-[2-(methyl-pyridin-2-ylamino)ethoxy]phenyl]propanoic acid\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[[5-[3-(quinolin-2-ylmethoxy)phenyl]tetrazol-2-yl]methyl]benzoic acid\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(C)OC(=O)N1CCC(CC1)OCc2onc(n2)c3ccncc3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H20N2O2S/c23-27(25,26)15-11-12-21-20(13-15)17-8-4-10-19(17)22(24-21)18-9-3-6-14-5-1-2-7-16(14)18/h1-9,11-13,17,19,22,24H,10H2,(H2,23,25,26)\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c(CS(=O)(=O)C)c(nc2ccccc12)c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" FC(F)(F)c1nnc2ccc(NCn3nnc4ccccc34)nn12\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1OC)S(=O)(=O)Nc2ccc(\\\\C=C\\\\C(=O)Nc3ccccc3N)cc2\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H20N4O2S/c18-17(23)21-13-9-14(11-5-2-1-3-6-11)24-15(13)16(22)20-12-7-4-8-19-10-12/h1-3,5-6,9,12,19H,4,7-8,10H2,(H,20,22)(H3,18,21,23)/t12-/m0/s1\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=N+1][Ring1][=Branch1][O-1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-propyl-4,5,6,7-tetrahydro-3h-azepin-2-amine\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CSc1ncccc1C(=O)NCCc2ccc(Cl)cc2\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" N[C@@H](Cc1ccc(F)cc1)C(=O)O\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][Branch1][C][C][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][O][C][Ring1][=N][=O]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=N][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1][N][C][=Branch1][C][=O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" cauliflower\\n\",\n        \"output\": \" cauliflower is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][S][Ring1][Branch1][C][Branch1][C][Cl][=C][Ring1][=C][Cl]\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc(N)c2cc(NCc3ccc(Cl)c(Cl)c3)ccc2n1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)c1cccc2c(cccc12)S(=O)(=O)Nc3cnccn3\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(2r)-3-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-2-hydroxypropyl]-1-oxo-2h-isoquinoline-4-carboxamide\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][Ring1][N]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C33H29F3N4O3/c1-3-43-27-16-14-26(15-17-27)40-31(38-29-9-5-4-8-28(29)32(40)42)22(2)39(21-24-7-6-18-37-20-24)30(41)19-23-10-12-25(13-11-23)33(34,35)36/h4-18,20,22H,3,19,21H2,1-2H3/t22-/m1/s1\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=N)c1cc2c(\\\\C=C\\\\c3ccc4OCOc4c3)cccc2s1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H25ClN4O3/c1-14(2)25-21(28)16-11-18(23)20(24-12-16)26-9-7-17(8-10-26)27-19-6-4-3-5-15(19)13-30-22(27)29/h3-6,11-12,14,17H,7-10,13H2,1-2H3,(H,25,28)\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][=Branch1][Ring1][#C]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10O4/c1-2-15-12(14)9-7-16-10-6-4-3-5-8(10)11(9)13/h3-7H,2H2,1H3\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" citizenship\\n\",\n        \"output\": \" citizenship is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H19N5O3/c31-25(32)22-10-3-1-7-19(22)15-30-28-24(27-29-30)18-8-5-9-21(14-18)33-16-20-13-12-17-6-2-4-11-23(17)26-20/h1-14H,15-16H2,(H,31,32)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C@@H1][Branch1][N][C][C@H1][C][C][C][=Branch1][C][=O][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][N][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H13Cl2NO3/c1-23-12-3-5-15-11(7-12)8-16(17(21)22)20(15)9-10-2-4-13(18)14(19)6-10/h2-8H,9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H11N3O/c13-9-5-1-2-6-10(9)15-12(16)11-7-3-4-8-14-11/h1-8H,13H2,(H,15,16)\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(benzoyl)-7-chloro-5-phenyl-3,5-dihydro-1h-1,4-benzodiazepin-2-one\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=N][C@H1][Branch1][Branch1][C][O][Ring1][Branch1][C][=Branch1][C][=O][N][O]\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C][N][Branch1][Ring2][C][C][O][C][=N][C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1][=C][N][=C][Branch2][Ring1][Ring2][N][=C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1][C][Ring1][N][=N][Ring2][Ring1][=Branch1][N][Branch1][Ring2][C][C][O][C][C][O]\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H13ClN2O4S2/c1-2-20-12(17)7-10-8-21-13(15-10)16-22(18,19)11-5-3-9(14)4-6-11/h3-6,8H,2,7H2,1H3,(H,15,16)\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H20FN3O2/c1-24(2)20(26)18(10-13-6-4-3-5-7-13)23-19(25)17-12-14-11-15(21)8-9-16(14)22-17/h3-9,11-12,18,22H,10H2,1-2H3,(H,23,25)/t18-/m0/s1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][N][Branch2][Ring2][=Branch2][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][#C][C][=C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Ring1][Branch2][C][Branch1][C][F][=C][Ring1][#C][N][=N][Ring2][Ring1][O]\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][=C][Branch1][#Branch2][N][C][C][O][C][=C][C][=Ring1][Branch1][C][=C][Ring1][S][Cl]\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-(2,4-dichlorophenyl)piperazin-1-yl]-2-(pyridin-2-ylmethoxy)ethanone\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][=C][Branch2][Ring1][C][N][=C][N][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)c1cnc(N[C@H]2CCCNC2)c3cc(sc13)c4ccc(F)cc4\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H30ClN3O/c1-5-27(6-2)13-7-8-16(3)25-23-19-11-9-17(24)14-22(19)26-21-12-10-18(28-4)15-20(21)23/h9-12,14-16H,5-8,13H2,1-4H3,(H,25,26)\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccc(NC(=O)c2cc(OCc3ccccc3)cc(OCc4ccccc4)c2)nc1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H19NOS/c16-14(15-8-4-1-5-9-15)13-12-7-3-2-6-11(12)10-17-13/h10H,1-9H2\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(CCOc1ccc(CC2SC(=O)NC2=O)cc1)c3ccccn3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H34FNO5/c1-15(2)25-21(11-10-19(29)12-20(30)13-23(31)32)24(17-6-8-18(27)9-7-17)22(14-33-5)26(28-25)16(3)4/h6-11,15-16,19-20,29-30H,12-14H2,1-5H3,(H,31,32)/b11-10+/t19-,20-/m1/s1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][N][=C][Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][S][C][=N][C][Branch1][C][C][=C][C][Branch1][C][C][=N][Ring1][Branch2][C][=Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H23N3O3/c1-13(2)9-22-17-12-21(10-14-5-7-15(25-4)8-6-14)11-16(17)18(23)20(3)19(22)24/h5-8,11-13H,9-10H2,1-4H3\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H23ClFN3O/c1-3-25(4-2)11-12-26-19-10-9-15(22)13-17(19)21(24-14-20(26)27)16-7-5-6-8-18(16)23/h5-10,13H,3-4,11-12,14H2,1-2H3\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][Branch1][C][O][=C][Branch1][C][O][C][=Branch1][Ring2][=C][Ring1][Branch2][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-(trifluoromethoxy)-1,3-benzothiazol-2-amine\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC[C@H](O)c1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-chloro-4-[3-(3-hydroxy-4-propanoyl-2-propylphenoxy)propylsulfanyl]phenyl]acetic acid\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cnc(nc1N(C)c2ccccc2)c3ccccn3\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)C(=O)Nc1ccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)cc1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[(3s)-1-[2-(2,3-dihydro-1-benzofuran-5-yl)ethyl]pyrrolidin-3-yl]-2,2-di(phenyl)acetamide\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2,5-dimethyl-1-(4-methylphenyl)-n-(4-methylphenyl)sulfonylpyrrole-3-carboxamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H12O3/c16-13-4-1-10(2-5-13)12-7-11-3-6-14(17)8-15(11)18-9-12/h1-8,16-17H,9H2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" thing\\n\",\n        \"output\": \" thing is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c(N)c(nc2ccccc12)c3cccc(F)c3)c4ccccc4\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[[2-methoxy-4-[(2-methylphenyl)sulfonylcarbamoyl]phenyl]methyl]-1-methyl-n-(2-phenylethyl)indole-5-carboxamide\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" growth\\n\",\n        \"output\": \" growth is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(NC(=O)c2ccc(c(C)c2)c3ccncc3)cc1N4CCN(C)CC4\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-chloro-n-(5-methyl-2-phenylpyrazol-3-yl)benzamide\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(9-chloro-5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n,n-dimethylpropan-1-amine\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H20FN7O2/c1-26-8-10-27(11-9-26)16-7-6-13(12-21-16)22-17(28)18-24-25-19(29-18)23-15-5-3-2-4-14(15)20/h2-7,12H,8-11H2,1H3,(H,22,28)(H,23,25)\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(ccc1N2CC[C@@H](O)C2)N3N=Nc4cc(sc4C3=O)c5ccc(Cl)cc5\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)c2ccc3cc(O)ccc3c2\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" albatross\\n\",\n        \"output\": \" albatross is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCc1c(O)c(O)c(C(=O)O)c2cc(Cc3ccccc3)c(C)cc12\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][Branch1][=Branch2][N][S][Ring1][=Branch1][=Branch1][C][=O][=O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring1][Branch1][C][=C][Ring2][Ring1][Ring1][Cl]\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][C][O][N][=C][Branch1][Ring2][N][=Ring1][Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-dimethylaminoethyl)-4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H18N4O2/c1-2-13(10-19-7-1)15-3-4-16(23-15)18-21-20-17(24-18)14-11-22-8-5-12(14)6-9-22/h1-4,7,10,12,14H,5-6,8-9,11H2\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H13NO4/c15-9-1-2-10-11(16)8-13(18-12(10)7-9)14-3-5-17-6-4-14/h1-2,7-8,15H,3-6H2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-[2,4-diamino-6-(phenylmethoxymethyl)pyrimidin-5-yl]phenyl]cyclopropanecarboxamide\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H19FN4O2S/c18-11-5-3-10(4-6-11)14-8-13(16(25-14)22-17(19)24)15(23)21-12-2-1-7-20-9-12/h3-6,8,12,20H,1-2,7,9H2,(H,21,23)(H3,19,22,24)/t12-/m0/s1\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(cccc34)C(F)(F)F\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C(Cc1nc2ccccc2[nH]1)c3nc4ccccc4[nH]3\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)c1ccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)cc1\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" [O-][N+](=O)c1ccc2[nH]ncc2c1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][O][C][C][=Branch1][C][=O][C][=C][C][=Branch1][C][=O][C][Ring1][=N][=Ring1][Branch2]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2NC(=O)C(NC(=O)c3ccccc3OC)N=C(c4ccccc4)c2c1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H11BrO3/c15-11-6-7-13(18-9-14(16)17)12(8-11)10-4-2-1-3-5-10/h1-8H,9H2,(H,16,17)\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H25ClN6O2/c1-32-11-7-19(8-12-32)34-23-4-2-3-21-24(23)25(30-16-29-21)31-17-5-6-22(20(26)13-17)33-15-18-14-27-9-10-28-18/h2-6,9-10,13-14,16,19H,7-8,11-12,15H2,1H3,(H,29,30,31)\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H6O4/c11-5-1-2-6(12)10-8(14)4-3-7(13)9(5)10/h1-4,11-12H\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[4-(4-acetylpiperazin-1-yl)phenyl]-5-[(2-fluorophenyl)amino]-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H20Cl2N2O3/c1-3-19-6-4-5-9(19)8-18-15(21)12-13(20)10(16)7-11(17)14(12)22-2/h7,9,20H,3-6,8H2,1-2H3,(H,18,21)/t9-/m0/s1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C@H1][Branch1][=N][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-amino-6-[4-(2-dimethylaminoethyl-ethylsulfamoyl)phenyl]-n-pyridin-3-ylpyrazine-2-carboxamide\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H28FN3O2/c1-16(2)27-12-4-5-18(14-27)15-28-17(3)26-23-11-10-21(13-22(23)24(28)29)30-20-8-6-19(25)7-9-20/h6-11,13,16,18H,4-5,12,14-15H2,1-3H3/t18-/m0/s1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(3,4-dichlorophenyl)-5,6-dihydroimidazo[2,1-b][1,3]thiazole\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(3-acetamido-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" cloth\\n\",\n        \"output\": \" cloth is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2,2,2-trifluoroethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-phenylpyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H27F3N2O/c1-3-29(4-2)23(30)19-10-8-17(9-11-19)22(18-12-14-28-15-13-18)20-6-5-7-21(16-20)24(25,26)27/h5-11,16,28H,3-4,12-15H2,1-2H3\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-thiophen-2-yl-3h-thieno[3,2-e]pyrimidin-4-one\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=Branch1][C][=O][N][C][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][Branch1][#C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][#Branch2][N][C][=N][C][=C][Branch1][C][C][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=N][Ring1][=C][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)S(=O)(=O)c2ccc(cc2F)c3cnc(N)c(n3)C(=O)Nc4cccnc4\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(2-diethylaminoethoxy)ethyl 1-phenylcyclopentane-1-carboxylate\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" FC(F)(F)c1nnc2ccc(nn12)N3CCCC3\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(methylsulfonylmethyl)-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C(Cc1ccccc1)NCc2ccccc2\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H29N3O/c1-19(32)29-27-17-28(24-8-4-2-7-22(24)27)12-14-31(15-13-28)18-20-10-11-26-23(16-20)21-6-3-5-9-25(21)30-26/h2-11,16,27,30H,12-15,17-18H2,1H3,(H,29,32)/t27-/m1/s1\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-furan-2-yl-n-methyl-3-thiophen-2-yl-3h-pyrido[3,2-f][1,4]diazepin-2-amine\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(2-ethoxyphenyl)phenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C32H38ClFN2O5S2/c1-4-36(32(37)19-23-5-9-29(10-6-23)42(2,38)39)28-13-16-35(17-14-28)18-15-31(25-20-26(33)22-27(34)21-25)24-7-11-30(12-8-24)43(3,40)41/h5-12,20-22,28,31H,4,13-19H2,1-3H3/t31-/m1/s1\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C30H35NO/c1-3-7-26(8-4-1)27-12-10-25(11-13-27)23-32-30-16-15-28-21-24(9-14-29(28)22-30)17-20-31-18-5-2-6-19-31/h1,3-4,7-8,10-13,15-16,22,24H,2,5-6,9,14,17-21,23H2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][=C][=N][C][=Branch1][=Branch2][=N][C][Ring1][=Branch1][Branch1][C][C][C][N][N]\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][NH1][C][Branch2][Ring1][Branch1][\\\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][\\\\-Ring1][O][Ring1][#Branch1][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][N][Branch1][#C][C][=Branch1][C][=O][C][=N][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)c3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][Ring1][N][C][=N+1][Branch1][C][C][C][Branch1][C][C][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" -0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-(3-bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[3,2-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@@H1][Branch1][C][C][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch1][P][C][C][C@@H1][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][Ring1][Branch2][C@@H1][Ring2][Ring1][=Branch1][Ring1][P]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C31H33N3O5S/c1-20-7-3-6-10-29(20)40(37,38)34-31(36)23-12-11-22(28(17-23)39-2)16-24-19-32-27-14-13-25(18-26(24)27)33-30(35)15-21-8-4-5-9-21/h3,6-7,10-14,17-19,21,32H,4-5,8-9,15-16H2,1-2H3,(H,33,35)(H,34,36)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" apple\\n\",\n        \"output\": \" apple is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2e,5s,6s,8z,11s)-5,6,15-trihydroxy-17-methoxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(14),2,8,15,17-pentaene-7,13-dione\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][Ring1][P][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H]([C@H](O)c1ccc(O)cc1)N2CCC(O)(CC2)c3ccccc3\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 8-chloro-6-(2-fluorophenyl)-1-methyl-4h-imidazo[1,5-a][1,4]benzodiazepine\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][N][=C][Branch1][Branch2][C][C][N][C][C][C][O][C][=C][C][Ring1][=N][=C][Ring1][P][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H26F3N3O7/c1-16(2)23(24(36)28(29,30)31)33-22(35)14-34-21(18-6-4-3-5-7-18)13-12-20(25(34)37)32-27(40)41-15-17-8-10-19(11-9-17)26(38)39/h3-13,16,23H,14-15H2,1-2H3,(H,32,40)(H,33,35)(H,38,39)\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-methoxy-4-morpholin-4-yl-2-pyridin-2-ylpyrimidine\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-methoxy-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)-4-oxo-1h-quinoline-2-carboxamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H11NO/c1-10(2)7-5-3-4-6-8(7)11-9(10)12/h3-6H,1-2H3,(H,11,12)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2,3-difluorophenyl)-2-[5-[[7-[3-[(2r)-2-(hydroxymethyl)pyrrolidin-1-yl]propoxy]quinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(4-chlorophenyl)-2-(1,2-dihydroimidazo[2,1-b]benzimidazol-4-yl)ethanone\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][C][S][=Branch1][C][=O][=Branch1][C][=O][O][C][=C][C][=C][Branch2][Ring1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch2][C][N][C][=C][N][=N][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1][C][=Branch1][Branch1][=N][Ring2][Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-(4-chlorophenyl)-2-methyl-3-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]quinazolin-4-one\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-chloro-2-[[4-(phenylmethylsulfonyl)-1,4-diazepan-1-yl]methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][N][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][=Branch2][N][=C][Ring1][=C][C][=Ring2][Ring1][C][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H21N7O2/c24-13-14-2-6-18(7-3-14)28-22(31)17-10-15-4-5-16(21(25)30-32)11-19(15)20(12-17)29-23-26-8-1-9-27-23/h1-12,32H,13,24H2,(H2,25,30)(H,28,31)(H,26,27,29)\\n\",\n        \"output\": \" -0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@]12CCC(=O)C=C1C=C[C@@H]3[C@@H]2CC[C@@]4(C)[C@H]3CC[C@@]45CCC(=O)O5\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1CCN(Cc2cnc(c(Cl)c2)c3ccc(cc3)C(=O)Nc4ccccc4N)CC1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][N][C][Ring1][Branch1][=C][C][=C][Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-phenylbicyclo[2.2.2]octan-4-amine\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H20N4O3/c1-28-19-7-6-17(20(26)24-13-15-4-2-8-22-11-15)10-18(19)21(27)25-14-16-5-3-9-23-12-16/h2-12H,13-14H2,1H3,(H,24,26)(H,25,27)\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H18ClNO/c1-19-8-7-13-9-16(18)17(20)10-14(13)15(11-19)12-5-3-2-4-6-12/h2-6,9-10,15,20H,7-8,11H2,1H3/t15-/m1/s1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][Branch2][Ring1][Ring2][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][=N][NH1][N][=Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" propan-2-yl 4-[1-(2-fluoro-4-methylsulfonylphenyl)pyrazolo[4,5-e]pyrimidin-4-yl]oxypiperidine-1-carboxylate\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C29H33FN6O4S/c1-39-25-14-23-24(15-26(25)40-11-3-8-36-9-6-19(17-37)7-10-36)32-18-33-28(23)35-29-31-16-22(41-29)13-27(38)34-21-5-2-4-20(30)12-21/h2,4-5,12,14-16,18-19,37H,3,6-11,13,17H2,1H3,(H,34,38)(H,31,32,33,35)\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3ccc[n+]([O-])c3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" pyrido[2,1-b]quinazolin-11-one\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1onc(NS(=O)(=O)c2ccc(N)cc2)c1\\n\",\n        \"output\": \" -0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H27N5O2/c1-16-13-23-22(26-21(16)24-17-7-5-4-6-8-17)25-18-9-11-20(12-10-18)29-15-19(28)14-27(2)3/h4-13,19,28H,14-15H2,1-3H3,(H2,23,24,25,26)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CSc1nc(C(=O)N)c(N)s1\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(9-ethylcarbazol-3-yl)morpholine-4-carboxamide\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfonyl-4-methanesulfonamido-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H12O5/c1-20-13-6-11(18)7-14-15(13)16(19)12(8-21-14)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[3-[[2-(3-dimethylamino-2,2-dimethylpropoxy)pyrimidin-4-yl]amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][Ring1][#Branch2][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C@@H1][Branch2][Ring2][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=N][C][C@H1][Branch1][C][O][C][C@@H1][Branch1][C][C][C][Ring1][O][=Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C31H30F4N4O2/c32-26-6-1-23(2-7-26)30(24-3-10-28(40)36-18-24)37-29(41)17-21-11-14-38(15-12-21)19-22-13-16-39(20-22)27-8-4-25(5-9-27)31(33,34)35/h1-10,13,16,18,20-21,30H,11-12,14-15,17,19H2,(H,36,40)(H,37,41)\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Nc1nccs1)c2ccccc2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[[5-[(2-cyclopentylacetyl)amino]-1h-indol-3-yl]methyl]-3-methoxy-n-(2-methylphenyl)sulfonylbenzamide\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H11N3/c1-2-4-10-9(3-1)5-6-11(15-10)12-13-7-8-14-12/h1-6H,7-8H2,(H,13,14)\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)CCN1C(=O)[C@@](O)(c2ccccc2Cl)c3c1cc(cc3C(F)(F)F)C(=O)N\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H10N2OS/c14-9-3-1-8(2-4-9)13-15-11-6-5-10(16)7-12(11)17-13/h1-7,16H,14H2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cnc(cn1)C(=O)NCCc2ccc(cc2)S(=O)(=O)NC(=O)NC3CCCCC3\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H15ClN4O3/c19-15-7-6-13(23-18(26)22-16(24)11-21-23)10-14(15)17(25)20-9-8-12-4-2-1-3-5-12/h1-7,10-11H,8-9H2,(H,20,25)(H,22,24,26)\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][Branch1][C][F][O][C][=C][C][=C][Branch1][=N][\\\\C][=C][/S][C][=Branch1][C][=O][N][C][\\\\-Ring1][=Branch1][=O][C][=C][Ring1][=C][O][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][C][C][Branch2][Branch1][Ring2][C][O][C][=N][C][=C][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=N][Ring2][Ring1][=N][C][Ring2][Ring2][Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2c(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)ncnc2cc1OCCCN(CCO)CC(C)C\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(2s)-4-methyl-1-oxo-1-[[(e,3s)-5-phenyl-1-phenylsulfonylpent-1-en-3-yl]amino]pentan-2-yl]morpholine-4-carboxamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[2,4-dimethoxy-5-[(2-methyl-2,3-dihydroindol-1-yl)sulfonyl]phenyl]acetamide\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-ethyl-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][O][Ring1][N]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" deficit\\n\",\n        \"output\": \" deficit is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-methyl-1,3,4-thiadiazol-2-amine\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" cd\\n\",\n        \"output\": \" cd is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H13N3O2/c1-21-14(12-7-9-19-10-8-12)11-15-16(18(21)22)17(20-23-15)13-5-3-2-4-6-13/h2-11H,1H3\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H20N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-10,13H,2-6H2,1H3,(H2,16,17,19)\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOC(=O)C1=Cc2ccc(O)cc2OC1=O\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][S][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl (2s)-2-(benzoylamino)-3-(4-nitrophenyl)propanoate\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-chloro-2-(pyridin-2-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H30NO3/c1-16(2)24(5,17(3)4)14-15-26-23(25)22-18-10-6-8-12-20(18)27-21-13-9-7-11-19(21)22/h6-13,16-17,22H,14-15H2,1-5H3/q+1\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4,5-dihydro-1h-imidazol-2-yl)quinoline\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc2ccc(F)cc2s1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H15Cl2N3O/c17-13-5-3-4-12(15(13)18)16(22)21-10-8-20(9-11-21)14-6-1-2-7-19-14/h1-7H,8-11H2\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[3-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]sulfamoyl]phenyl]acetamide\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H29N7O2/c1-15-19-14-27-24(28-20-8-7-18(13-26-20)30-11-9-25-10-12-30)29-22(19)31(17-5-3-4-6-17)23(33)21(15)16(2)32/h7-8,13-14,17,25H,3-6,9-12H2,1-2H3,(H,26,27,28,29)\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-[(4-methoxyphenyl)methyl]-2,4,8-trioxo-6-phenyl-1h-pyrido[3,4-d]pyrimidin-7-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@@][Branch1][C][O][Branch2][Ring2][Ring1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H26FN5O2/c1-15-4-9-19(23)20(12-15)26-21-10-11-24-22(27-21)25-16-5-7-18(8-6-16)30-14-17(29)13-28(2)3/h4-12,17,29H,13-14H2,1-3H3,(H2,24,25,26,27)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccnc(NCc2ccccc2)c1\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCCC1c2cccnc2\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(1,3-benzodioxol-5-yloxy)-2-(4-imidazol-1-ylphenoxy)-6-methylpyrimidine\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccc(OCCc2ccccc2)cc1\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H24F3N3S/c1-25-11-13-26(14-12-25)9-4-10-27-17-5-2-3-6-19(17)28-20-8-7-16(15-18(20)27)21(22,23)24/h2-3,5-8,15H,4,9-14H2,1H3\\n\",\n        \"output\": \" 4.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H20N4O2S/c18-17(23)21-16-13(15(22)20-12-7-4-8-19-10-12)9-14(24-16)11-5-2-1-3-6-11/h1-3,5-6,9,12,19H,4,7-8,10H2,(H,20,22)(H3,18,21,23)/t12-/m0/s1\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(nc2c(cc(F)cc12)N3CCN(C)CC3)C(=O)Nc4ccc(cc4)N5CCOCC5\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" propan-2-yl 4-[[7-(2-fluoro-4-methylsulfonylphenyl)-5,6-dihydropyrrolo[3,2-e]pyrimidin-4-yl]oxy]piperidine-1-carboxylate\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][=C][Branch1][#C][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring2][Ring1][#Branch1][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [5-amino-1-(4-fluorophenyl)pyrazol-4-yl]-[3-[(2r)-2,3-dihydroxypropoxy]phenyl]methanone\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H24O3/c1-12-9-14(11-17(2,3)10-12)20-16(19)15(18)13-7-5-4-6-8-13/h4-8,12,14-15,18H,9-11H2,1-3H3\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC(=O)c1snnc1c2ccccc2\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H10N2OS/c12-10(14)6-11-13-9(7-15-11)8-4-2-1-3-5-8/h1-5,7H,6H2,(H2,12,14)\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)CCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1c(N)sc2CCCCc12\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(3-fluorophenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C1CNCC(C1)c2nc3ccccc3s2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][=C][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][Branch1][#Branch2][N][=C][Ring1][=Branch1][N][Branch1][C][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H23F2N3O/c1-15(26)23-13-16-2-4-17(5-3-16)14-24-8-10-25(11-9-24)20-7-6-18(21)12-19(20)22/h2-7,12H,8-11,13-14H2,1H3,(H,23,26)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" quinazoline\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-2-[(3-chlorophenyl)methyl]isoindole-1,3-dione\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][Branch1][=C][O][N][=C][Ring1][Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][C][=C][O][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch2][Ring1][#C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][#C][C][N][C][=Branch1][C][=O][O][C@H1][C][C][O][C][Ring1][Branch1][=C][Ring1][S][=C][C][=C][Ring2][Ring1][#Branch2][C][O][C][=N][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H19NO/c1-4-14(5-2)11(3)13(15)12-9-7-6-8-10-12/h6-11H,4-5H2,1-3H3\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(ccc1Cn2ncc3ccc(NC(=O)CC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6,7-dimethoxy-n-[3-methyl-4-(pyridin-2-ylmethoxy)phenyl]quinazolin-4-amine\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-pyridin-2-yl-1h-benzimidazole\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H9Cl2N3O/c13-8-3-1-4-9(7-8)16-17-12(18)10-5-2-6-15-11(10)14/h1-7,16H,(H,17,18)\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[[2-(bis(2-hydroxyethyl)amino)-4,8-di(piperidin-1-yl)pyrimido[6,5-e]pyrimidin-6-yl]-(2-hydroxyethyl)amino]ethanol\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][=C][C][=C][NH1][N][=C][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H11N3O/c1-9-4-6-10(7-5-9)16-12-11(13(17)15-16)3-2-8-14-12/h2-8H,1H3,(H,15,17)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc(SCc2ccccc2)nc3c1ncn3[C@@H]4O[C@H](CO)[C@@H](O)[C@H]4O\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C]\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCOc1ccc(cc1)c2cc(C(=O)N)c(NC(=O)N)s2\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch1][O][C][O][C][C][O][C][Branch1][C][C][C][C][=C][Ring1][=C]\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][#Branch1][C][C][=Branch1][C][=O][N][C][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-methyl-5-[2-[4-(trifluoromethyl)-3h-imidazol-2-yl]pyridin-4-yl]oxy-n-[4-(trifluoromethyl)phenyl]benzimidazol-2-amine\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" FC(F)(F)c1nnc2ccc(nn12)n3ccnc3\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[3,5-bis(trifluoromethyl)phenyl]-2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxamide\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-ethyl-2-(4-methylsulfonylphenyl)-n-[1-[(3r)-3-(4-methylsulfonylphenyl)-3-(3,4,5-trifluorophenyl)propyl]piperidin-4-yl]acetamide\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][=N][C][=C][Ring2][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H18F2N4OS/c20-14-4-3-10(6-15(14)21)16-7-12-17(27-16)13(18(22)26)9-24-19(12)25-11-2-1-5-23-8-11/h3-4,6-7,9,11,23H,1-2,5,8H2,(H2,22,26)(H,24,25)/t11-/m0/s1\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](CO)Nc1nc(SCc2ccccc2)nc3nc(N)sc13\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H23N5O3S/c1-15-5-6-17-13-16(2)21-24-25-23(28(21)18(17)12-15)32-14-20(29)26-7-9-27(10-8-26)22(30)19-4-3-11-31-19/h3-6,11-13H,7-10,14H2,1-2H3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20N2O3S/c1-2-13-3-6-15(20-12-13)9-10-24-16-7-4-14(5-8-16)11-17-18(22)21-19(23)25-17/h3-8,12,17H,2,9-11H2,1H3,(H,21,22,23)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H34F2N2O4/c1-4-5-6-7-8-16-30(25(33)29-23-14-11-20(27)18-22(23)28)17-15-19-9-12-21(13-10-19)34-26(2,3)24(31)32/h9-14,18H,4-8,15-17H2,1-3H3,(H,29,33)(H,31,32)\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][=C][C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H21N3O2/c1-2-22-17-6-4-3-5-15(17)16-13-14(7-8-18(16)22)20-19(23)21-9-11-24-12-10-21/h3-8,13H,2,9-12H2,1H3,(H,20,23)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cn1cnc(c2ccccc2)c1c3cc4c(N)ncnc4s3\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][Branch2][Ring1][Ring1][C][O][C@H1][C][C][C][N][C@H1][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][Ring2][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)c1ccccc1Cn2nnc(n2)c3cccc(OCc4ccc5ccccc5n4)c3\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H](c1ncncc1F)[C@](O)(Cn2cncn2)c3ccc(F)cc3F\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch2][Ring1][Ring1][O][C][=Branch1][C][=O][N][C][C][N][C][C][C][Ring1][#Branch1][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-diethyl-4-[(2-methoxyphenyl)-piperidin-4-ylidenemethyl]benzamide\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H23ClF3N3O3/c1-3-28(4-2)9-10-29-17-12-13(19(27)30)11-15(22(24,25)26)18(17)21(32,20(29)31)14-7-5-6-8-16(14)23/h5-8,11-12,32H,3-4,9-10H2,1-2H3,(H2,27,30)/t21-/m1/s1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H20N2O5/c1-4-5-9-6-10(7-12(20-2)13(9)21-3)15-16-11(8-22-15)14(18)17-19/h6-7,11,19H,4-5,8H2,1-3H3,(H,17,18)/t11-/m1/s1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][Branch2][Ring2][Ring2][N][C][=N][C][=N][C][=C][C][Branch1][=C][O][C][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][Branch1][Ring1][O][C][C][=C][Ring2][Ring1][Branch1][Ring1][P][=C][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][C][C][C][C@H1][Ring1][Branch1][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(F)c(F)c1C(=O)c2cnc(NC3CCN(CC3)S(=O)(=O)C)nc2N\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=N][C][=N][C][=C][Ring1][=Branch1][N][=C][N][Ring1][Branch1][C][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C38H48N4O5/c43-34-19-17-31(32-18-20-36(45)41-37(32)34)35(44)27-39-23-11-4-2-1-3-5-12-24-42-25-21-29(22-26-42)47-38(46)40-33-16-10-9-15-30(33)28-13-7-6-8-14-28/h6-10,13-20,29,35,39,43-44H,1-5,11-12,21-27H2,(H,40,46)(H,41,45)/t35-/m0/s1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][N][C][C@H1][Branch1][C][C][C][N][Branch1][C][C][C][C][Ring1][P][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring2][=Branch2][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch2][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)NC(=O)NN2CCCCCC2\\n\",\n        \"output\": \" 0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(CCc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n-diethyl-4-(5-hydroxyspiro[chromene-2,4'-piperidine]-4-yl)benzamide\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=N][C][=C][N][Ring1][Branch1][C][C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(cc1)c2cn3ccccc3n2\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H31F2N7O3/c1-2-9-36(11-12-37)10-4-13-39-19-7-8-20-23(16-19)30-17-31-27(20)33-24-14-18(34-35-24)15-25(38)32-22-6-3-5-21(28)26(22)29/h3,5-8,14,16-17,37H,2,4,9-13,15H2,1H3,(H,32,38)(H2,30,31,33,34,35)\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H23NO2/c22-19(17-10-4-1-5-11-17)20(23,18-12-6-2-7-13-18)16-21-14-8-3-9-15-21/h1-2,4-7,10-13,23H,3,8-9,14-16H2\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[2-[5-[(3-methyloxetan-3-yl)methoxy]benzimidazol-1-yl]quinolin-8-yl]piperidin-4-amine\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)COc1ccc(Cl)cc1CN2CCN(CC2)S(=O)(=O)Cc3ccccc3\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H8N2O3S/c9-14(11,12)5-7-6-3-1-2-4-8(6)13-10-7/h1-4H,5H2,(H2,9,11,12)\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 8-(4-phenylphenyl)-1-azabicyclo[2.2.2]octan-8-ol\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@][Branch2][Ring2][=Branch1][C][C][C][N][Ring1][Branch1][C][N][=C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][C][=C][C][=C][N][Ring1][Branch1][N][=Ring2][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][N][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H19ClN4O3S/c1-24(2)17(26)10-25-15-6-4-3-5-11(15)7-14(20(25)28)22-18(27)13-8-12-9-16(21)29-19(12)23-13/h3-6,8-9,14,23H,7,10H2,1-2H3,(H,22,27)\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,2-di(phenyl)-n-(3-piperidin-1-ylpropyl)acetamide\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)N5N=CC(=O)NC5=O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CCCN1c2ccccc2CCc3ccc(Cl)cc13\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(7-methyl-2-thiophen-2-ylimidazo[3,2-a]pyridin-3-yl)benzamide\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl]-n-pyridin-2-ylcyclohexanecarboxamide\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(2s,3r)-3-hydroxy-4-[(3-methoxyphenyl)methylamino]-1-phenylbutan-2-yl]-n',n'-dipropylbenzene-1,3-dicarboxamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=N][N][C][C][=C][Branch2][Ring1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][NH1][N][=Ring1][S][=C][Ring2][Ring1][#Branch1][C][=C][Ring2][Ring1][O][O][C]\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H14Cl2N2O3/c21-12-9-15(22)17-14(18(20(26)27)23-16(17)10-12)8-11-6-7-24(19(11)25)13-4-2-1-3-5-13/h1-5,8-10,23H,6-7H2,(H,26,27)/b11-8+\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-chloro-3-(2,6-dichlorophenyl)-[1,2,4]triazolo[4,5-a]pyridine\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ncnc(NS(=O)(=O)c2ccc(N)cc2)c1OC\\n\",\n        \"output\": \" -0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H17NO5/c1-26-18(23)8-4-7-17(22)21-12-9-10-15-16(11-12)13-5-2-3-6-14(13)19(24)20(15)25/h2-3,5-6,9-11H,4,7-8H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(cyclopentylmethyl)-1-[[2-methoxy-4-(phenylsulfonylcarbamoyl)phenyl]methyl]indole-6-carboxamide\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][S][=Branch1][C][=N][=Branch1][C][=O][C][C][=N][O][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H23N3O/c1-20(14-18(24)23(2)19(21)22-20)12-11-15-7-6-10-17(13-15)16-8-4-3-5-9-16/h3-10,13H,11-12,14H2,1-2H3,(H2,21,22)\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cc(F)cc(Cl)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H32Cl2N4O4S/c1-29(2)18-3-6-22(7-4-18)36(33,34)28-25(32)31-13-9-19(10-14-31)30-15-11-20(12-16-30)35-21-5-8-23(26)24(27)17-21/h3-8,17,19-20H,9-16H2,1-2H3,(H,28,32)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H19N3O3S/c1-23(20,21)12-14-11-15(19-7-9-22-10-8-19)18-16(17-14)13-5-3-2-4-6-13/h2-6,11H,7-10,12H2,1H3\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(CCN1CCCCC1)(C2CCCCC2)c3ccccc3\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H13N3/c1-2-6-12(7-3-1)10-16-15-13-8-4-5-9-14(13)17-11-18-15/h1-9,11H,10H2,(H,16,17,18)\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" phenylmethyl n-[2-(4-fluorophenyl)-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cccc(NC(=O)CC23CC4CC(CC(C4)C2)C3)c1C\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H24N4O3/c1-25-17-5-3-16(4-6-17)14-26-19(24)23-11-7-15(8-12-23)13-22-18-20-9-2-10-21-18/h2-6,9-10,15H,7-8,11-14H2,1H3,(H,20,21,22)\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][C][=Branch1][C][=O][N][Ring1][O][C][C][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-methyl-9-propan-2-ylcarbazol-3-yl)morpholine-4-carboxamide\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)CCNC(=O)c1cc(Br)c(N)cc1OC\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(3-ethylamino-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(Cc1cc(I)c(Oc2ccc(O)c(I)c2)c(I)c1)C(=O)O\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][C][=C][NH1][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC1=CN=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccc(F)cc2\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2c(Nc3ccc(NC(=O)c4ccccc4)cc3)ncnc2cc1OCCCN5CCOCC5\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OCC(=O)N1CCC[C@@H]1COc2cccc3ncnc(Nc4ccc(OCc5ccccn5)c(Cl)c4)c23\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[4-amino-2-(ethoxymethyl)imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18FN5O3/c20-15-3-1-2-4-16(15)22-19-24-23-18(28-19)17(26)21-13-5-7-14(8-6-13)25-9-11-27-12-10-25/h1-8H,9-12H2,(H,21,26)(H,22,24)\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H21NO4/c1-18-12-8-9-13(18)15(17(20)21-2)14(10-12)22-16(19)11-6-4-3-5-7-11/h3-7,12-15H,8-10H2,1-2H3\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H18N6S/c1-11-12(2)23-15-13(11)14(19-10-20-15)21-6-8-22(9-7-21)16-17-4-3-5-18-16/h3-5,10H,6-9H2,1-2H3\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[4-[3-(4-bromophenoxy)-2-hydroxypropyl]piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Brc1cnc(Nc2cccc(NC(=O)N3CCCC3)c2)nc1NCCCNC(=O)c4cccs4\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H10N2OS/c1-2-3-5-4-6(10)9-7(11)8-5/h4H,2-3H2,1H3,(H2,8,9,10,11)\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Ring2][O][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][Branch1][C][Ring1][O][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)CCOC(=O)C1(CCCCC1)C2CCCCC2\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3c(cccc3n1CC(=O)O)c4cnccn4\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NS(=O)(=O)c1ccc(CCNc2ccc3nnc(c4ccccc4)n3n2)cc1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-hydroxy-6-(phenylmethyl)pyrano[3,2-c]quinoline-4,5-dione\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][Branch1][S][N][C][N][N][=N][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][=N][N][Ring2][Ring1][Ring2][Ring1][P]\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H15ClFNO2S/c1-10-14(20)7-8-15-17(10)18(11(2)21(15)9-16(22)23)24-13-5-3-12(19)4-6-13/h3-8H,9H2,1-2H3,(H,22,23)\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C29H29F3N6O6S/c30-29(31,32)11-16-45(41,42)44-25-8-7-24(26(36-25)28(40)33-17-19-9-14-43-15-10-19)35-27(39)23-6-5-20(18-38-13-12-34-37-38)21-3-1-2-4-22(21)23/h1-8,12-13,19H,9-11,14-18H2,(H,33,40)(H,35,39)\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][=Branch1][=C][C][Ring1][#Branch1][=O][C@H1][Branch2][Ring1][#Branch2][C][C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][Ring2][Ring1][N][N][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1CCC[C@H](C1)C(=O)N2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=N][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Ring1][O][C][=C][C][C][Branch1][C][N][=N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCC(=O)Nc1ccc(Cl)c(c1)c2oc3cccnc3n2\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2-chloro-5-methoxyphenyl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccccc1C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][Branch1][#C][C][=C][N][=C][Ring1][=Branch1][N][C][C][N][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][Ring2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][Ring2][=C][N][=C][Ring1][#Branch1][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3/t14-/m1/s1\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][C][=C][Branch1][Ring1][C][O][C][Branch1][Ring1][C][O][=C][Ring1][#Branch2][O]\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H24ClFN4O3/c1-29-20-12-16-19(13-21(20)31-8-2-5-28-6-9-30-10-7-28)25-14-26-22(16)27-18-4-3-15(23)11-17(18)24/h3-4,11-14H,2,5-10H2,1H3,(H,25,26,27)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[[3-(1,4-diazepane-1-carbonyl)-4-fluorophenyl]methyl]-2h-phthalazin-1-one\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc2c(c1)c(Sc3ccccc3Cl)c(C)n2CC(=O)O\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" report\\n\",\n        \"output\": \" report is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cccc(NS(=O)(=O)c2cccc3nonc23)c1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" gauge\\n\",\n        \"output\": \" gauge is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][C][C@H1][Branch2][Ring2][C][C][N][C][=Branch2][Ring1][O][=N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][O][C][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][C][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-hydroxy-3-(4-hydroxyphenyl)-5-methoxychromen-4-one\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OCC4CCNCC4\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-amino-5-oxo-7-propan-2-ylchromeno[3,2-e]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-methyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-yl)-2-phenylacetamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc2C(=O)C=C(Oc2c1)N3CCOCC3\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H]1CN(C[C@H](C)N1)c2c(F)c(N)c3C(=O)C(=CN(C4CC4)c3c2F)C(=O)O\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][Branch2][Ring1][#Branch1][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=N][C][NH1][C][=C][C][Ring1][=Branch2][=Ring1][Branch1][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O]\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OC[C@@H]4CCCN(C)C4\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C32H37N7O4/c1-22-5-6-24(36-32(40)23-7-8-33-30(17-23)39-12-14-42-15-13-39)18-26(22)37-31-25-19-29(43-16-11-38-9-3-4-10-38)28(41-2)20-27(25)34-21-35-31/h5-8,17-21H,3-4,9-16H2,1-2H3,(H,36,40)(H,34,35,37)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccc(NC(=S)N2CCC(CC2)C(=O)c3ccc(F)cc3)cc1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1CCO[C@@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc(cc1)[N+](=O)[O-]\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(=O)Nc1ccc2C(=O)NC(=O)c2c1\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14ClNS/c15-13-4-2-1-3-11(13)9-16-7-5-14-12(10-16)6-8-17-14/h1-4,6,8H,5,7,9-10H2\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch1][N][C][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9N3/c11-10-12-7-6-9(13-10)8-4-2-1-3-5-8/h1-7H,(H2,11,12,13)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(OC)c(CNc2n[nH]c3ccnc(Oc4ccccc4)c23)c1\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H11N3OS/c1-13-10(14)12-9(15-13)11-7-8-5-3-2-4-6-8/h2-6H,7H2,1H3,(H,11,12,14)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H18ClN5O4/c1-26(2)21(31)23-13-6-3-11(4-7-13)10-27-20(30)16-17(19(29)25-27)24-15-9-12(22)5-8-14(15)18(16)28/h3-9H,10H2,1-2H3,(H,23,31)(H,24,28)(H,25,29)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16N4O3S/c21-24(22,20-7-9-23-10-8-20)14-4-1-3-13(11-14)15-12-19-6-2-5-17-16(19)18-15/h1-6,11-12H,7-10H2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC[C@H](C)Oc1cc(Oc2ccccc2)cc(c1)C(=O)Nc3ccc(cn3)C(=O)O\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1CCC[C@@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(OC2CCN(CC2)C3CCN(CC3)C(=O)C4=CNC(=O)c5ccccc45)cc1Cl\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C(=O)O)c1ccc(c(F)c1)c2ccccc2\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC[C@H](C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@@H]12\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[3-[(2-chloropyrimidin-4-yl)amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-2-[[7-amino-2-[(2,3-difluorophenyl)methylsulfanyl]pteridin-4-yl]amino]propan-1-ol\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H23NO3/c23-20(25-19-15-22-13-11-16(19)12-14-22)21(24,17-7-3-1-4-8-17)18-9-5-2-6-10-18/h1-10,16,19,24H,11-15H2\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H8N4O2S/c17-9(7-4-2-1-3-5-7)16-12-15-8-10(18)13-6-14-11(8)19-12/h1-6H,(H,13,14,18)(H,15,16,17)\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][N][=C][Branch1][#Branch2][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][C][=C][Branch1][#Branch1][S][C][Ring1][S][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1Cc2ccccc2N1NC(=O)c3ccc(Cl)c(c3)S(=O)(=O)N\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7,9-dichloro-3,5-dihydro-2h-pyridazino[4,5-b]indole-1,4-dione\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][N][C][=Branch1][C][=O][C@@H1][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H24N6O3/c1-15-11-20(26-22(25-15)27-10-8-23-13-27)28-9-2-3-17(28)21(29)24-7-6-16-4-5-18-19(12-16)31-14-30-18/h4-5,8,10-13,17H,2-3,6-7,9,14H2,1H3,(H,24,29)/t17-/m1/s1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[1-(2-morpholin-4-ylethyl)benzimidazol-2-yl]-3-nitrobenzamide\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1NC(=O)c2cc(OCc3ccccc3)ccc12\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H10BrClN2O2/c1-16-13(19)10-6-9(12(14)17-10)11(18)7-2-4-8(15)5-3-7/h2-6,17H,1H3,(H,16,19)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H21FN6O3/c1-14(29)27-10-12-28(13-11-27)16-8-6-15(7-9-16)23-19(30)20-25-26-21(31-20)24-18-5-3-2-4-17(18)22/h2-9H,10-13H2,1H3,(H,23,30)(H,24,26)\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1c(F)cc(cc1c2ccc(cn2)C(=O)NCC(C)(C)C)C(=O)NC3CC3\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-thiophen-2-ylpyrimidin-2-amine\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][S][O][C][=C][C][=C][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][Ring2][=C][Ring1][P][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cccc(Nc2ccccc2C(=O)O)c1C\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" lyric\\n\",\n        \"output\": \" lyric is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-amino-5-bromo-n-(2-diethylaminoethyl)-2-methoxybenzamide\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-(4-chlorophenyl)-1,3,5-triazine-2,4-diamine\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)COc1ccc(cc1c2ccc(Cl)cc2)C(F)(F)F\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H6F2N2/c9-7(10)8-11-5-3-1-2-4-6(5)12-8/h1-4,7H,(H,11,12)\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(N)C(=O)N[C@H](COCc1ccccc1)C(=O)N2CCC3(CC2)CN(c4ccccc34)S(=O)(=O)C\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H17N/c1-3-7-14(8-4-1)11-12-16-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(7s)-1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5h-benzo[d]heptalen-7-yl]acetamide\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(=C(N2C1=O)C(=O)OCOC(=O)C(C)(C)C)SC3CN(C3)C4=NCCS4\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][#Branch2][C][N][C][C][N][C][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-phenyl-1,2,4-thiadiazol-5-amine\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(N)Cc1c[nH]c2ccc(OCc3cccs3)cc12\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][C][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][=Branch1][C][=O][C][=C][Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][O][C][Ring1][P]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)C3CC3\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][O][C][=C][C][Branch2][Ring1][#C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][Branch1][=Branch1][C][=C][Ring1][#Branch1][Cl][C][Branch1][C][F][Branch1][C][F][F][=C][C][=C][Ring2][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4-fluorophenyl)-[(3s)-3-[3-(4-fluorophenyl)-1,2,4-oxadiazol-5-yl]piperidin-1-yl]methanone\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)c2ccnc(N)n2\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H9NO/c14-8-5-6-10-9-3-1-2-4-11(9)13(15)12(10)7-8/h1-7H,14H2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)[C@@H]2Sc3ccccc3N(CCN(C)C)C(=O)[C@@H]2OC(=O)C\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1cc(cc(N2CCCC2)c1Oc3ccccc3)C(=O)O\\n\",\n        \"output\": \" -0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H8N6O/c8-5-4-6(13-7(9)12-5)10-1-3(2-14)11-4/h1,14H,2H2,(H4,8,9,10,12,13)\\n\",\n        \"output\": \" -0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][Branch1][Ring1][C][N][C][C][Branch1][Ring1][C][O][C][Ring1][#Branch2]\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5r)-3-thiophen-2-ylspiro[1,3-oxazolidine-5,8'-1-azabicyclo[2.2.2]octane]-2-one\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H16N2O/c1-11-7-8-15-14(9-11)16-10-12-5-3-4-6-13(12)17-2/h3-9H,10H2,1-2H3,(H,15,16)\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H17ClO3/c15-11-6-7-13(18-9-14(16)17)12(8-11)10-4-2-1-3-5-10/h6-8,10H,1-5,9H2,(H,16,17)\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)c1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(benzoyl)-3-methyl-3,5-dihydro-2h-1,5-benzodiazepin-4-one\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)-7-methoxy-6-[2-(4-methylpiperazin-1-yl)ethoxy]quinazolin-4-amine\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H14F3N5O/c1-10(15-14(19)5-20-7-22-15)16(25,6-24-9-21-8-23-24)12-3-2-11(17)4-13(12)18/h2-5,7-10,25H,6H2,1H3/t10-,16+/m0/s1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1cc(O)c2C(=O)C(=COc2c1)c3ccc(F)cc3\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-7-(2-morpholin-4-ylethoxy)-5-propan-2-yloxyquinazolin-4-amine\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(Nc1nccs1)c2cccnc2\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-chloro-2-(1-pyridin-4-ylpropyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" [O-][S+](c1ccccc1)c2ccc3nnnn3n2\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-cyclopropylsulfonylphenyl)-n-(5-fluoro-1,3-thiazol-2-yl)-3-(oxan-4-yl)propanamide\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (1r)-7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-hydroxy-5-[(1r)-1-hydroxy-2-[2-[4-[[(2r)-2-hydroxy-2-phenylethyl]amino]phenyl]ethylamino]ethyl]phenyl]formamide\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H12O3S/c15-14(12-7-3-1-4-8-12)11-18(16,17)13-9-5-2-6-10-13/h1-10H,11H2\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[(7-chloroquinolin-4-yl)amino]pentyl-ethylamino]ethanol\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H7NO4/c16-13-11-4-2-1-3-9(11)10-6-5-8(15(18)19)7-12(10)14(13)17/h1-7H\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][O][C@H1][C][C][C@][Branch1][Ring1][C][=O][C@H1][C][C][C@][Branch1][C][C][C@H1][Branch2][Ring1][Branch2][C][C][C@][Ring1][=Branch1][Branch1][C][O][C@@H1][Ring1][O][C][C][C@][Ring1][P][Branch1][C][O][C][Ring2][Ring1][=Branch1][C][=C][C][=Branch1][C][=O][O][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(NC(=O)c2cccc(c2)N3CCOCC3)cc1NC(=O)c4ccc(OCc5ccccn5)cc4\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][C][O][C][=C][C][=N][C][=C][C][Branch1][P][N][C][=C][C][Branch1][C][O][=C][Branch1][C][Cl][C][=C][Ring1][Branch2][F][=C][Ring1][S][C][=C][Ring2][Ring1][Ring2][O][C]\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][N][=N][C][Ring1][O][C][=C][C][=C][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)NCC(O)COc1cccc2[nH]ccc12\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2c(c1)c([S+]([O-])c3ccc(Cl)cc3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCSc1ccc2nc(NC(=O)OC)[nH]c2c1\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C28H30N2O/c31-28-27-14-8-7-13-24(27)21-30(28)25-15-18-29(19-16-25)20-17-26(22-9-3-1-4-10-22)23-11-5-2-6-12-23/h1-14,25-26H,15-21H2\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-fluoro-2-thiophen-2-yl-1,2-dihydroquinazolin-4-amine\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-methyl-4-phenylthiadiazole-5-carboxamide\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(Cl)c(Nc2ncnc3cc(OC)cc(OC4CCN(C)CC4)c23)c1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H29N7O/c1-16(2)30-17(3)25-15-22(30)21-9-10-24-23(27-21)26-19-5-7-20(8-6-19)29-13-11-28(12-14-29)18(4)31/h5-10,15-16H,11-14H2,1-4H3,(H,24,26,27)\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-chloro-2-[[(3s)-3-ethyl-4-phenylsulfonylpiperazin-1-yl]methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H16N2OS/c1-11-5-7-12(8-6-11)10-17-14(18)13-4-3-9-16-15(13)19-2/h3-9H,10H2,1-2H3,(H,17,18)\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[4-methyl-2-[(2-oxo-1h-indol-3-ylidene)methyl]-1h-pyrrol-3-yl]propanoic acid\\n3-[4-methyl-2-[(z)-(2-oxo-1h-indol-3-ylidene)methyl]-1h-pyrrol-3-yl]propanoic acid\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(CCN1CCCC1)(C2CCCCC2)c3ccccc3\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)Nc1sc(cc1C(=O)N)c2ccccc2\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H26ClNO3/c26-22-6-5-20(18-1-3-19(4-2-18)24(29)30)10-21(22)23(28)27-14-25-11-15-7-16(12-25)9-17(8-15)13-25/h1-6,10,15-17H,7-9,11-14H2,(H,27,28)(H,29,30)\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][Branch2][Ring2][Ring1][N][C][=N][C][=N][C][=C][C][Branch1][Ring1][O][C][=C][C][Branch1][=N][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][Ring2][Ring1][Ring2][Ring1][S][=C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][P][C][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][C][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=N][C][=N][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=C][Ring2][Ring1][Branch2][C][=C][Ring2][Ring1][N][O][C]\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-(2,3-dihydroxypropyl)-1,3-dimethylpurine-2,6-dione\\n\",\n        \"output\": \" -1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1NCCc2[nH]c(cc12)c3ccncc3\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H25ClN2O3/c25-21-2-1-17(18-6-19(23(29)30)12-26-11-18)7-20(21)22(28)27-13-24-8-14-3-15(9-24)5-16(4-14)10-24/h1-2,6-7,11-12,14-16H,3-5,8-10,13H2,(H,27,28)(H,29,30)\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=N][C][Branch1][C][N][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOc1ccc(cc1)N2C(=Nc3ccccc3C2=O)CC\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C5H7N3OS2/c1-10-5-8-2(3(6)9)4(7)11-5/h7H2,1H3,(H2,6,9)\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-n-[(1s)-2-[(3ar,7as)-6-(2-phenylethyl)-3,3a,4,5,7,7a-hexahydro-2h-pyrrolo[2,3-c]pyridin-1-yl]-1-cyclohexyl-2-oxoethyl]-2-methylaminopropanamide\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][S][C][=Branch1][=Branch1][=N][C][Ring1][Branch1][=O][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H14N2O2/c16-12-10-6-7-11(14-10)13(17)15(12)8-9-4-2-1-3-5-9/h1-5,10-11,14H,6-8H2\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H24ClFN4O3/c1-14-11-26(12-15-2-5-17(23)6-3-15)8-9-27(14)20(28)13-30-19-7-4-16(22)10-18(19)25-21(24)29/h2-7,10,14H,8-9,11-13H2,1H3,(H3,24,25,29)/t14-/m1/s1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H15ClN2O4S2/c1-2-25-17(22)15-6-4-3-5-14(15)16-11-26-18(20-16)21-27(23,24)13-9-7-12(19)8-10-13/h3-11H,2H2,1H3,(H,20,21)\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[4-[[3-(phenoxy)phenyl]methoxy]phenyl]propanoic acid\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" girdle\\n\",\n        \"output\": \" girdle is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch2][Ring1][#Branch2][C][C][O][C][=C][C][=C][Branch1][=N][C][C][S][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=O][C][=C][Ring1][=C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H14N6O2S/c18-26(24,25)13-6-4-12(5-7-13)21-17-19-9-8-14(22-17)15-11-20-16-3-1-2-10-23(15)16/h1-11H,(H2,18,24,25)(H,19,21,22)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" earth\\n\",\n        \"output\": \" earth is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=S(=O)(Cc1cc(nc(n1)c2ccccn2)N3CCOCC3)c4ccccc4\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)C(=O)N1CCC(CC1)C(=O)NCc2cccs2\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-oxo-6-phenyl-3-(phenylsulfonylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)OC(=O)N1CCC(CC1)Oc2ncnc(Oc3cccnc3C)c2C\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][Branch1][C][Cl][=C][C][C][=Branch1][C][=O][N][N][C][=Branch1][C][=O][C][=Ring1][Branch2][NH1][C][Ring1][O][=C][Ring1][S]\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][=Branch1][O][C][=C][C][N][=C][Branch2][Ring1][Branch1][NH1][C][=Ring1][Branch1][C][=C][Ring1][=Branch2][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring2][Ring1][=C]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2c(Nc3ccc(Cl)cc3F)ncnc2cc1OCCn4cncn4\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" octagon\\n\",\n        \"output\": \" octagon is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H20N6O4/c1-7(2)8(14)12(21)23-4-3-22-6-19-5-16-9-10(19)17-13(15)18-11(9)20/h5,7-8H,3-4,6,14H2,1-2H3,(H3,15,17,18,20)/t8-/m0/s1\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][Ring2][N][C][C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H24N2O4/c1-5-6-12(4,7-17-10(13)15)8-18-11(16)14-9(2)3/h9H,5-8H2,1-4H3,(H2,13,15)(H,14,16)\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)N(C(C)C)c1nnc(N)s1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H17NO/c1-8-5-4-6-9(2)11(8)13-7-10(3)12/h4-6,10H,7,12H2,1-3H3/t10-/m1/s1\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-n-[2-chloro-4-(piperidine-1-carbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][=C][N][=C][Branch1][C][Cl][N][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][Ring2][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H28Cl2N4O/c1-2-23-7-3-4-15(13-23)14-24-8-10-25(11-9-24)19(26)22-16-5-6-17(20)18(21)12-16/h5-6,12,15H,2-4,7-11,13-14H2,1H3,(H,22,26)/t15-/m1/s1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][N][C][=C][N][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H14F3NO4S/c1-15(22,16(17,18)19)14(21)20-11-7-9-13(10-8-11)25(23,24)12-5-3-2-4-6-12/h2-10,22H,1H3,(H,20,21)\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(4-bromo-2-phenylphenoxy)acetic acid\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1ccc(Nc2nccc(n2)c3ccccc3)cc1\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H31N5O4/c1-29-7-9-31(10-8-29)23-16-20(34-2)15-21-24(32)17-22(28-25(21)23)26(33)27-18-3-5-19(6-4-18)30-11-13-35-14-12-30/h3-6,15-17H,7-14H2,1-2H3,(H,27,33)(H,28,32)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)O\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][=Branch1][N][Branch1][C][C][C][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H26N2O2/c1-14(2)17(18(22)20-12-6-7-13-20)19-16(21)11-10-15-8-4-3-5-9-15/h3-5,8-9,14,17H,6-7,10-13H2,1-2H3,(H,19,21)/t17-/m0/s1\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" sharon\\n\",\n        \"output\": \" sharon is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC1(CCN(Cc2c[nH]c3ccccc23)CC1)c4ccc(Cl)cc4\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1=C(OCc2ccccc2)C(=O)C=CO1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][C][Branch1][C][C][C][O][C][=N][C][=C][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=N][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H37N3O2/c1-18-3-6-24-23(5-4-22(29-24)7-9-28-8-2-10-31)26(18)30-25(32)17-27-14-19-11-20(15-27)13-21(12-19)16-27/h3-6,19-21,28,31H,2,7-17H2,1H3,(H,30,32)\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1sc2ncnc(SCC(=O)N3CCN(CC3)C(=O)c4occc4)c2c1C\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" death\\n\",\n        \"output\": \" death is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(4s)-4-hydroxy1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)-6-(quinolin-4-ylmethyl)thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10N2O/c18-14-11-6-2-4-8-13(11)17-9-10-5-1-3-7-12(10)16-15(14)17/h1-8H,9H2\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc(Cl)cc1C(=O)Nc2ccccc2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H29ClN4O6/c1-33-13-16(28)12-26-19(29)11-25-27(21(26)31)15-6-7-18(23)17(10-15)20(30)24-14-22(32)8-4-2-3-5-9-22/h6-7,10-11,16,28,32H,2-5,8-9,12-14H2,1H3,(H,24,30)/t16-/m1/s1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@](O)(C(=O)Nc1ccc(cc1Cl)S(=O)(=O)NCCCO)C(F)(F)F\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H24N2O4S/c1-2-3-6-21-24-14-19(12-18(23(28)29)13-20-5-4-11-30-20)25(21)15-16-7-9-17(10-8-16)22(26)27/h4-5,7-12,14H,2-3,6,13,15H2,1H3,(H,26,27)(H,28,29)/b18-12+\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-chloro-1h-indole\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(3,4-dichlorophenyl)-piperidin-4-ylidenemethyl]-n,n-diethylbenzamide\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=N][C][Branch1][P][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Ring2][=N][Ring1][S][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch1][Ring2][S][Ring1][Branch1][N][C][C@@][Branch1][N][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][O][C][Ring1][N][=O]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H24F3N3O5S/c1-16(2)22(23(33)25(26,27)28)29-21(32)15-31-20(17-9-5-3-6-10-17)14-13-19(24(31)34)30-37(35,36)18-11-7-4-8-12-18/h3-14,16,22,30H,15H2,1-2H3,(H,29,32)\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][C][C][C][C][C][N][Ring1][#Branch2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-(4-chlorophenyl)-2-methylfuran-3-carboxylic acid\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C@H1][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][N][Branch1][C][C][C][C][=C][S][C][=Branch1][Ring2][=N][Ring1][Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C@H1][Branch2][Ring1][S][C][C@H1][Branch1][C][O][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][N][=C][S][Ring1][Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=CC(=O)Oc2c3CCCNc3c(C)cc12\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H14N2O2S/c19-18(20)17-9-13-12(2-1-3-16(13)23-17)6-4-11-5-7-14-15(8-11)22-10-21-14/h1-9H,10H2,(H3,19,20)/b6-4+\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][O][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[2,2,2-trichloro-1-(4-hydroxyphenyl)ethyl]phenol\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[S+]([O-])c1ccc(\\\\C=C/2\\\\C(=C(CC(=O)O)c3cc(F)ccc23)C)cc1\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(2,4-dichloro-3-methylphenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][Ring1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Ring1][=Branch1][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-cyclohexylcyclohexanamine\\n\",\n        \"output\": \" -0.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H33ClN2O/c25-22-2-1-17(7-16-3-5-26-6-4-16)11-21(22)23(28)27-15-24-12-18-8-19(13-24)10-20(9-18)14-24/h1-2,11,16,18-20,26H,3-10,12-15H2,(H,27,28)\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nc(N)c(c(COCc2ccccc2)n1)c3ccc(NC(=O)C4CC4)cc3\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H24N6O/c1-13(2)26-14(3)22-12-18(26)17-10-11-21-20(24-17)23-16-8-6-15(7-9-16)19(27)25(4)5/h6-13H,1-5H3,(H,21,23,24)\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H36N2O3S/c1-4-6-7-8-9-16-22(5-2)17-10-11-20(23)18-12-14-19(15-13-18)21-26(3,24)25/h12-15,20-21,23H,4-11,16-17H2,1-3H3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)c2csc(n2)N(CCCN3CCOCC3)C(=O)c4occc4\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccccc1NC(=O)c2ccc(CNc3nccc(n3)c4cccnc4)cc2\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[(4-chlorophenyl)-phenylmethyl]-4-methyl-1,4-diazepane\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" FC(F)c1nc2ccccc2[nH]1\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2nccc(Nc3cccc(Cl)c3)n2)cc1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n'-(4-fluorophenyl)-6-methylpyrimidine-2,4-diamine\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)c3cc4c(cn(C)c4cc3Cl)C(=O)C(=O)N(C)C\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)n2nc(cc2NC(=O)Nc3ccc(OCCN4CCOCC4)c5ccccc35)C(C)(C)C\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][NH1][C][Branch1][C][N][=C][Ring1][=Branch1][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n,n-dimethyl-n'-(thiophen-2-ylmethyl)piperidine-1,4-dicarboxamide\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(NC(=O)C=C)cc1\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H13NO3/c13-11(12-6-8-14-9-7-12)15-10-4-2-1-3-5-10/h1-5H,6-9H2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (e)-3-[4-[(z)-1,2-di(phenyl)but-1-enyl]phenyl]prop-2-enoic acid\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1CC(NC(=O)C)c2ccccc2N1C(=O)c3ccccc3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H19N3O2S/c1-13(2)7-9-10(11(17)14-8-13)19-12(15-9)16-3-5-18-6-4-16/h3-8H2,1-2H3,(H,14,17)\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ncnc2[nH]ccc12\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=N][C][=C][Ring1][Branch1][C][=C][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][C][C][Ring1][Ring1][C][=Branch1][C][=O][N][Branch1][#Branch1][C][C][C][C][Ring1][Ring1][C][Ring1][S][=N][N][Ring2][Ring1][Ring1][C][C][=C][C][=N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2,3-dihydro-[1,3]oxazolo[2,3-b]quinazolin-5-one\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H14F3N3O4S2/c16-15(17,18)10-7-11-13(8-12(10)26(19,22)23)27(24,25)21-14(20-11)6-9-4-2-1-3-5-9/h1-5,7-8,14,20-21H,6H2,(H2,19,22,23)\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H14N4/c1-3-7-13(8-4-1)18-15-11-12-17-16(20-15)19-14-9-5-2-6-10-14/h1-12H,(H2,17,18,19,20)\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[2-(dipropylamino)ethyl]-1,3-dihydroindol-2-one\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[(3z)-6-fluoro-2-methyl-3-[(4-methylsulfinylphenyl)methylidene]inden-1-yl]acetic acid\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[4-(2,4-dichlorophenyl)piperazin-1-yl]-2-(pyridin-4-ylmethoxy)ethanone\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-[3-(2-chlorophenothiazin-10-yl)propyl]piperazin-1-yl]ethanol\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)C1CCN(CC1)c2ncccc2c3ccc(Cl)c(c3)C(=O)NCC4CCCCCC4\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H18N2O5S/c18-25(22,23)15-11-12(17(20)21)10-14(19-8-4-5-9-19)16(15)24-13-6-2-1-3-7-13/h1-3,6-7,10-11H,4-5,8-9H2,(H,20,21)(H2,18,22,23)\\n\",\n        \"output\": \" -0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3c(C)n[nH]c3C)c2C(=O)N4C[C@H](O)CO4\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Brc1ccc(cc1)C(=O)Cn2cnc3ccccc23\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H16N2O/c1-2-17-12-7-5-11(6-8-12)13-10-15-14-4-3-9-16(13)14/h5-8,10H,2-4,9H2,1H3\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 8-chloro-6-(4-methylpiperazin-1-yl)benzo[b][1,5]benzoxazepine\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring1][N][C][O][C][=C][C][Branch1][C][F][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][Branch1][Branch2][C][C][O][C][C][Ring1][=Branch1][O][C][=C][C][=C][Ring2][Ring1][N][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(naphthalene-1-carbonylamino)-n-(oxan-4-ylmethyl)pyridine-2-carboxamide\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]naphthalene-2-carboxamide\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-dimethyl-7h-purin-6-amine\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H19ClN4O3S/c1-30-19-10-15(6-7-18(19)26-9-8-16(28)12-26)27-22(29)21-17(24-25-27)11-20(31-21)13-2-4-14(23)5-3-13/h2-7,10-11,16,28H,8-9,12H2,1H3/t16-/m1/s1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccccc1NC(=O)c2cc(ccc2Cl)[N+](=O)[O-]\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOc1ccc2C=CC(=O)Oc2c1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(4-chlorophenyl)methyl]-1,3,4-thiadiazol-2-amine\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[1-hydroxy-2-[1-(4-hydroxyphenyl)propan-2-ylamino]ethyl]benzene-1,3-diol\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H27F3N4O6S/c1-16(2)24(25(37)27(28,29)30)32-23(36)15-34-22(18-8-5-4-6-9-18)13-12-21(26(34)38)33-41(39,40)20-11-7-10-19(14-20)31-17(3)35/h4-14,16,24,33H,15H2,1-3H3,(H,31,35)(H,32,36)\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H21NO4/c1-22-17-6-5-13(10-18(17)23-2)9-16-15-12-20(25-4)19(24-3)11-14(15)7-8-21-16/h5-8,10-12H,9H2,1-4H3\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][=C][O][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][C][Ring1][=C]\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1=C(Oc2c(cccc2C1=O)C(=O)OCCN3CCCCC3)c4ccccc4\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" twine\\n\",\n        \"output\": \" twine is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][N][Branch2][Ring1][O][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccccc34)c2C(=O)N5C[C@@H](O)[C@@H](O)C5\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H11FO2/c21-18-8-4-3-5-13(18)12-9-10-15-14-6-1-2-7-16(14)19(22)20(23)17(15)11-12/h1-11H\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C32H39ClN2O5S2/c1-4-35(32(36)22-24-8-12-29(13-9-24)41(2,37)38)28-16-19-34(20-17-28)21-18-31(26-6-5-7-27(33)23-26)25-10-14-30(15-11-25)42(3,39)40/h5-15,23,28,31H,4,16-22H2,1-3H3/t31-/m1/s1\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)c2ccc(Nc3ncc(C)c(Nc4cccc(c4)S(=O)(=O)NC(C)(C)C)n3)cc2\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [1-[9-[[(2r)-2-hydroxy-2-(8-hydroxy-2-oxo-1h-quinolin-5-yl)ethyl]amino]nonyl]piperidin-4-yl] n-(2-phenylphenyl)carbamate\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cn1c(Nc2ccc(cc2)C(F)(F)F)nc3cc(Oc4ccnc(c4)c5ncc([nH]5)C(F)(F)F)ccc13\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)c2ccc(Nc3ccnc4ccccc34)cc2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc2Sc3ccccc3N(C[C@H](C)CN(C)C)c2c1\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamoyloxymethyl]benzoic acid\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)Cc1ccccc1Nc2c(Cl)cccc2Cl\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H12ClN3O3S/c1-8(9-4-5-25-7-9)21-17(24)13-14(16(23)20-21)19-12-6-10(18)2-3-11(12)15(13)22/h2-8H,1H3,(H,19,22)(H,20,23)\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C34H37N3O8S2/c1-36(19-8-13-24-9-4-2-5-10-24)47(44,45)30-22-29(31(38)33(40)32(30)39)34(41)37-20-17-26-14-15-28(21-27(26)23-37)46(42,43)35-18-16-25-11-6-3-7-12-25/h2-7,9-12,14-15,21-22,35,38-40H,8,13,16-20,23H2,1H3\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][N][=C][Branch2][Ring2][Branch2][N][C][=Branch1][C][=O][C][Branch1][#Branch2][C][C][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring1][Ring1][S][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(4-chlorophenyl)-2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]propanamide\\n\",\n        \"output\": \" 4.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccc(cc1)c2nnn(Cc3ccccc3F)n2\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCC(CO)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)ccc4[nH]3\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-2-(4-cyclopropylsulfonylphenyl)-n-(5-fluoro-1,3-thiazol-2-yl)-3-(oxan-4-yl)propanamide\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1CN[C@H]2CCCN[C@H]2c3ccccc3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][Branch2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][O][=C][N][=C][Ring1][#Branch1][C][Branch1][C][C][C][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H18N2O4/c1-17-8-3-4-11(18-2)9(5-8)10(15)7-14-12(16)6-13/h3-5,10,15H,6-7,13H2,1-2H3,(H,14,16)\\n\",\n        \"output\": \" -0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][C][C][=C][Branch1][#Branch2][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-amino-n-(3-methoxypyrazin-2-yl)benzenesulfonamide\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[(3,4-dichloro-5-methyl1h-pyrrole-2-carbonyl)amino]piperidin-1-yl]-1,3-thiazole-4-carboxylic acid\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C@@H1][O][C][=Branch1][C][=O][C][C@@H1][Ring1][=Branch1][N][C][=Branch1][C][=O][C@@H1][C][C][C][N][N][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][C][Ring1][Branch2][=O][N][C][=Branch1][C][=O][C][=N][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" pigeon\\n\",\n        \"output\": \" pigeon is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=C][N][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][F][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H16ClNO2S/c1-11-6-7-16-15(8-11)18(12(2)20(16)10-17(21)22)23-14-5-3-4-13(19)9-14/h3-9H,10H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(4s)-4-hydroxy1,2-oxazolidine-2-carbonyl]-3-methyl-6-[(2-methylaminobenzimidazol-1-yl)methyl]-1-(2-methylpropyl)thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H19N3O3S/c1-28(26,27)24-19-5-3-2-4-17(19)18-14-16(7-8-20(18)24)23-21(25)9-6-15-10-12-22-13-11-15/h2-5,7-8,10-14H,6,9H2,1H3,(H,23,25)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H7N7O2S/c1-15-4-14-7(16(17)18)9(15)19-8-5-6(11-2-10-5)12-3-13-8/h2-4H,1H3,(H,10,11,12,13)\\n\",\n        \"output\": \" 0.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1Cl)[C@]23CNC[C@H]2C3\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl-methylamino]-1-methylpiperidine-4-carboxamide\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H30FN7O/c1-15(2)32-16(3)26-14-21(32)22-20(25)13-27-24(30-22)29-18-7-5-17(6-8-18)23(33)28-19-9-11-31(4)12-10-19/h5-8,13-15,19H,9-12H2,1-4H3,(H,28,33)(H,27,29,30)\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H27ClN2/c1-20-6-5-7-21(18-20)19-27-14-16-28(17-15-27)25(22-8-3-2-4-9-22)23-10-12-24(26)13-11-23/h2-13,18,25H,14-17,19H2,1H3\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-chloro-n-[1-[2-(1,3-dihydroxypropan-2-ylamino)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15N/c1-2-6-12(7-3-1)15-10-13-8-4-5-9-14(13)11-16-15/h1-9,15-16H,10-11H2\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cccc(NC(=O)c2cccc(Cc3c(C)nn(CCO)c3c4ccccc4)c2)c1\\n\",\n        \"output\": \" 4.29\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-(2,6-dichlorophenyl)-2-(2,4-difluorophenyl)sulfanylpyridazino[6,1-f]pyrimidin-6-one\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N]\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOc1ccc(NC(=O)C)cc1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-n-(2,2,2-trifluoroethyl)benzenesulfonamide\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][C@@H1][Branch1][C][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][O][Ring1][N]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-hydroxy-n-(1,3-thiazol-2-yl)benzenesulfonamide\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)Cc3cccc(c3)C(=O)O)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][Branch2][C][N][C][C][C][S][C][C][N][C][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch2][Ring2][C][C][C][C][N][Branch2][Ring1][=Branch1][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" naphthalene\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H28N4O2/c1-18-16-20(4-6-22(18)19-8-10-26-11-9-19)25(30)27-21-5-7-24(31-3)23(17-21)29-14-12-28(2)13-15-29/h4-11,16-17H,12-15H2,1-3H3,(H,27,30)\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-nitro-2-phenylphenoxy)acetic acid\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1(CC(=O)NC(=N1)N)c2ccccc2\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccnc(NS(=O)(=O)c2ccc(N)cc2)n1\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][C][O][C@@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[2-[2,5-dimethyl-1-(phenylmethyl)pyrrol-3-yl]-2-oxoethyl]-5-(trifluoromethyl)pyridin-2-one\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16N2O/c1-12-8-9-18-17(10-12)19-11-15-14-5-3-2-4-13(14)6-7-16(15)20/h2-10,20H,11H2,1H3,(H,18,19)\\n\",\n        \"output\": \" 4.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][S][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-hydroxy-3-(4-hydroxyphenyl)-4-methylchromen-2-one\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][C][N][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-nitrophenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-dimethylaminoethyl)-5-[(z)-(5-fluoro-2-oxo-1h-indol-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(O)c3)c2cc1OC\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][Branch1][P][\\\\C][=C][\\\\C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2][=C][Ring1][P]\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[3-(2-dimethylaminoethyl)-1h-indol-5-yl]-n-methylmethanesulfonamide\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H17ClN2O2/c1-12-3-6-19-17(9-12)21(13(2)24(19)11-20(25)26)16-7-8-23-18-10-14(22)4-5-15(16)18/h3-10H,11H2,1-2H3,(H,25,26)\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(Cc1ccc(O)cc1)NCC(O)c2cc(O)cc(O)c2\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1)c2nnc(N3CCN(CC3)C(=O)c4occc4)c5ccccc25\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" ONC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H9N3O3S/c1-5-7(6(4-13)12-15-5)8(14)11-9-10-2-3-16-9/h2-3,13H,4H2,1H3,(H,10,11,14)\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H20ClN3O4S/c1-28(26,27)17-5-3-13(10-16(17)20)15(9-12-2-4-14(24)8-12)19(25)23-18-11-21-6-7-22-18/h3,5-7,10-12,15H,2,4,8-9H2,1H3,(H,22,23,25)/t12-,15+/m0/s1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][C][C][N][Branch2][Ring1][Ring2][C][C][=Branch1][C][=O][N][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H21NO2/c1-12(14-8-5-9-18-14)10-15(17)16-11-13-6-3-2-4-7-13/h2-4,6-7,12,14H,5,8-11H2,1H3,(H,16,17)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2,2-dimethylpropanoyloxymethyl (4r,5s,6s)-3-[1-(4,5-dihydro-1,3-thiazol-2-yl)azetidin-3-yl]sulfanyl-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (s)-[(4s,5r,7r)-5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl]-(6-methoxyquinolin-4-yl)methanol\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=N][C][=C][Ring1][=Branch1][N][=C][Branch2][Ring1][C][S][C][=N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][S][Ring1][#Branch2][N][Ring1][S][C][C][O]\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1SC(=NC1=O)NCc2ccccc2\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCC1(CC)C(=O)NC(=O)NC1=O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H24N6O3S/c1-4-25-14(2)21-13-18(25)17-9-10-20-19(24-17)23-15-5-7-16(8-6-15)29(26,27)22-11-12-28-3/h5-10,13,22H,4,11-12H2,1-3H3,(H,20,23,24)\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H40N4O5S/c1-19-16-22(32-5)17-20(2)24(19)34(30,31)26(4)14-15-33-18-23(29)28-12-10-27(11-13-28)21-6-8-25(3)9-7-21/h16-17,21H,6-15,18H2,1-5H3\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" fuel\\n\",\n        \"output\": \" fuel is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc2cc(C)c3nnc(SCC(=O)N4CCN(CC4)C(=O)c5occc5)n3c2cc1C\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)[C@@H]1N(C)c2ccccc2C[C@@H](CO)NC1=O\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][C][=C][C][=Branch2][Ring1][#Branch1][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1OC(=Cc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccccc1NC(=O)Nc2ccccc2\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-chloro-4-[3-[(3-ethyl-7-propyl-1,2-benzoxazol-6-yl)oxy]propylsulfanyl]phenyl]acetic acid\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[5-[2-(2,3-dihydroindol-1-yl)-2-oxoethyl]sulfanyl-1,3,4-oxadiazol-2-yl]-n,n-diethylbenzenesulfonamide\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2N=CC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-phenyl-1-benzothiophene-2-carboximidamide\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCC(O)CN1CCN(CC1)c2ccccc2\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(NCc2ccccc2)nc3ccccc13\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-amino-4-dimethylaminothieno[5,4-b]pyridine-2-carboxamide\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][Branch1][C][F][=C][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=N][Ring2][Ring1][S]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1CNCCO)c2ccc3c(nc(nc3n2)N4C[C@@H](C)O[C@@H](C)C4)N5CCOCC5\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][Branch1][=Branch2][C][C][O][C][=C][C][=Ring1][Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][P][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=N][C][=Branch1][N][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(phenoxy)-3-pyrrolidin-1-yl-5-sulfamoylbenzoic acid\\n\",\n        \"output\": \" -0.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)cc1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(4-acetylphenyl)sulfonyl-1-cyclohexylurea\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=C][N][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=N][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][=C][Ring1][=C][C][=C][Ring2][Ring1][C][O][C]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1h-benzimidazol-2-ylmethyl)-n-(5,6,7,8-tetrahydroquinolin-8-yl)butane-1,4-diamine\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC[C@H](O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)ccc4[nH]3\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccccc1O\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][=C][Ring1][=N]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" chromen-4-one\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(phenoxy)-1-phenylethanone\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1N=C(c2ccccc2Cl)c3cc(Cl)ccc3NC1=O\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][C][=Branch2][Ring1][P][=C][Branch2][Ring1][Ring1][C][Ring1][#Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][=Branch1][C][=O][O][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Branch1][C][C][C][=C][C][Ring1][#Branch1][=N][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch2][Branch1][Ring1][=N][C][=Ring1][Branch1][C][C][O][C][=C][C][=C][Branch2][Ring1][S][C][C@H1][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)c1[nH]c2cc(Cl)cc(Cl)c2c1\\\\C=C\\\\C(=O)Nc3ccccc3\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (3e)-3-(2-chlorothioxanthen-9-ylidene)-n,n-dimethylpropan-1-amine\\n3-(2-chlorothioxanthen-9-ylidene)-n,n-dimethylpropan-1-amine\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][C@H1][C][C@@H1][Branch1][C][C][C][=C][C][=C][C@H1][Branch1][C][C][C@H1][Branch2][Ring1][C][C][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][C@@H1][Ring2][Ring1][#Branch1][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H20N2O6S2/c1-13(12-23)27-16-9-14(19(24)22-20-21-7-8-29-20)10-17(11-16)28-15-3-5-18(6-4-15)30(2,25)26/h3-11,13,23H,12H2,1-2H3,(H,21,22,24)/t13-/m0/s1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12N2O/c16-15(18)17-13-7-3-1-5-11(13)9-10-12-6-2-4-8-14(12)17/h1-10H,(H2,16,18)\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H30FN5O5/c1-16(2)37-22-13-18(34-11-10-31-6-8-32(9-7-31)17(3)33)12-20-23(22)26(29-14-28-20)30-24-19(27)4-5-21-25(24)36-15-35-21/h4-5,12-14,16H,6-11,15H2,1-3H3,(H,28,29,30)\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-2-[[2-amino-5-(phenylmethylsulfanyl)-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-amino-n-[(4-methoxyphenyl)methyl]-4,6-dimethylthieno[5,4-b]pyridine-2-carboxamide\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(CC12CC3CC(CC(C3)C1)C2)Nc4cccc5ncccc45\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H](NC(=O)c1cccc2CCN(Cc3ccc(Cl)cc3)c12)c4ccc(cc4)C(=O)O\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7,7-dimethyl-2-morpholin-4-yl-6,8-dihydro-5h-[1,3]thiazolo[5,4-c]azepin-4-one\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C(Nc1nc2ccccc2[nH]1)c3ccccc3\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring1][S]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1N=C(N)N=C(N)N1c2ccc(Cl)cc2\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Branch1][C][N][C][Ring1][O][=C][Ring1][#C]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C32H39FN2O5S2/c1-4-35(32(36)22-24-8-12-29(13-9-24)41(2,37)38)28-16-19-34(20-17-28)21-18-31(26-6-5-7-27(33)23-26)25-10-14-30(15-11-25)42(3,39)40/h5-15,23,28,31H,4,16-22H2,1-3H3/t31-/m1/s1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H23BrN2O3/c1-4-19-9-5-6-11(19)10-18-16(20)14-13(21-2)8-7-12(17)15(14)22-3/h7-8,11H,4-6,9-10H2,1-3H3,(H,18,20)/t11-/m0/s1\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1nc2ccccn2c1c3ccnc(Nc4cccc(Cl)c4)n3\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][=C][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][Ring1][=Branch2][C][Branch1][C][F][=C][Ring1][S]\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2ccnc(Nc3ccccc3)n2\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][C][Branch1][C][O][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)C([C@@H]1CCN(CCc2ccc3OCCc3c2)C1)(c4ccccc4)c5ccccc5\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccccc1CN2CCC(CC2)N3CCC(CC3)N4C(=O)Nc5ccccc45\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" naphthalen-1-ol\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][N][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C@H1][Branch1][C][O][C][O]\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][Branch2][Ring2][#C][C][C][O][C][=C][C][=C][Branch2][Ring1][S][C][C@H1][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][#Branch2][=C][Branch1][C][C][S][Ring2][Ring2][Ring1]\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H18N4S2/c1-11(2)13-7-3-4-8-14(13)17-15-18-16(20-19-15)22-10-12-6-5-9-21-12/h3-9,11H,10H2,1-2H3,(H2,17,18,19,20)\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n-dimethyl-3-[1-(phenylmethyl)indazol-3-yl]oxypropan-1-amine\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-methoxy-n-(7-methoxy-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepin-3-yl)benzamide\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5,7-dimethoxy-3-(4-methoxyphenyl)chromen-4-one\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-propyl-2-sulfanylidene-1h-pyrimidin-4-one\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)S(=O)(=O)Nc2nccs2\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-5-chloro-n-(2-diethylaminoethyl)-2-methoxybenzamide\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2,5-dimethyl-3-[8-(trifluoromethyl)quinolin-4-yl]indol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][N][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-phenyl-1,3,4-thiadiazol-2-amine\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H26N4O4/c1-27-8-6-15(7-9-27)31-20-13-16(28-2)12-18-21(20)23(25-14-24-18)26-17-4-3-5-19-22(17)30-11-10-29-19/h3-5,12-15H,6-11H2,1-2H3,(H,24,25,26)\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1cc2[nH]cnc2cc1Cl\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][NH1][C][Branch2][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=Branch1][C][=O][O][=C][Branch1][C][Cl][C][=Ring2][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H11FN2O4S/c1-21(19,20)12-7-2-9(8-16(12)18)13(17)15-11-5-3-10(14)4-6-11/h2-8H,1H3,(H,15,17)\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" c1ccc2ncccc2c1\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H15NO4/c1-3-15(4-2)10-6-5-9-7-11(13(16)17)14(18)19-12(9)8-10/h5-8H,3-4H2,1-2H3,(H,16,17)\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc(Cl)nc(NCc2ccccc2)n1\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccc(cc1)n2cc(C3CCNCC3)c4cc(Cl)ccc24\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-phenyl-1,3,5-triazine-2,4-diamine\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-hydroxy-2-morpholin-4-ylchromen-4-one\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN([C@H](CN1CCCC1)c2ccccc2)C(=O)Cc3ccc(Cl)c(Cl)c3\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][S][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][P][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-fluorophenyl)-2-[2-[[7-[3-[4-(hydroxymethyl)piperidin-1-yl]propoxy]-6-methoxyquinazolin-4-yl]amino]-1,3-thiazol-5-yl]acetamide\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H8F3N5/c11-10(12,13)6-3-1-2-5(4-6)7-16-8(14)18-9(15)17-7/h1-4H,(H4,14,15,16,17,18)\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1N(Cc2ccccc12)C3CCN(CCC(c4ccccc4)c5ccccc5)CC3\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][=C][Branch1][C][N][N][=C][Branch1][C][N][N][Ring1][=Branch2][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][=C][Ring1][#C]\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(phenylmethoxy)isoindole-1,3-dione\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H8FN3/c10-7-3-1-6(2-4-7)8-5-12-9(11)13-8/h1-5H,(H3,11,12,13)\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[4-[[6-[(2,4-difluorophenyl)amino]pyrimidin-4-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(4-aminophenyl)sulfonylaniline\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring2][Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][=Branch1][S+1][Branch1][C][C][O-1][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H12O3/c18-15-10-3-4-11-16(15)20-17(19)14-9-5-7-12-6-1-2-8-13(12)14/h1-11,18H\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][S][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][=N]\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][Branch2][Ring2][Branch2][C][N][C][C][C][C][C][C][=Ring1][=Branch1][C][=C][Branch2][Ring1][C][N][=C][Branch1][#Branch1][N][=C][Ring1][=N][Ring1][=Branch1][N][C][C][C][C][Ring1][Branch1][N][C][C][C][C][Ring1][Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)c2c(onc2c3ccccc3)C=C1c4ccncc4\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch2][Ring1][S][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-cyclobutyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3-yl]benzamide\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[1-(2-amino-2-oxoethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-2-chloro-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 10-[2-(1-methylpiperidin-2-yl)ethyl]-2-methylsulfanylphenothiazine\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10O4/c16-11-4-1-9(2-5-11)13-7-10-3-6-12(17)8-14(10)19-15(13)18/h1-8,16-17H\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(CN(C)C)CN1c2ccccc2CCc3ccccc13\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" guarantee\\n\",\n        \"output\": \" guarantee is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=N][C][Branch1][C][N][=N][C][=C][Ring1][#Branch1][N][=C][N][Ring1][Branch1][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O]\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H33F2N7O4/c1-3-8-37(10-11-38)9-5-12-41-24-16-22-19(15-23(24)40-2)28(32-17-31-22)34-25-13-18(35-36-25)14-26(39)33-21-7-4-6-20(29)27(21)30/h4,6-7,13,15-17,38H,3,5,8-12,14H2,1-2H3,(H,33,39)(H2,31,32,34,35,36)\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c(SCCCO)c(Cc3ccccc3C(F)(F)F)sc12\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)c2cc3cc(Br)ccc3[nH]2\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-tert-butyl-3-[[5-methyl-2-[[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino]pyrimidin-4-yl]amino]benzenesulfonamide\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])NC(=O)c2ccccc2\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-chloro-2-[(5-chlorothiophen-2-yl)sulfonylamino]-n-(4-morpholin-4-ylsulfonylphenyl)benzamide\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H24N2O2/c1-3-13-11(2)17-14-5-4-12(16(19)15(13)14)10-18-6-8-20-9-7-18/h12,17H,3-10H2,1-2H3\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-[[(2r)-1-hydroxy-4-methylpentan-2-yl]amino]-5-[(1s)-1-phenylethyl]sulfanyl-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11N3O2S/c13-10(16)8-6-9(7-4-2-1-3-5-7)18-11(8)15-12(14)17/h1-6H,(H2,13,16)(H3,14,15,17)\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][F][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][Branch1][Ring1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch2][Ring2][Ring1][C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][N][Ring2][Ring1][N][C]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@@H1][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][=N][C][=C][C][=C][Branch1][=Branch2][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H31NO/c22-20(18-10-4-1-5-11-18,19-12-6-2-7-13-19)14-17-21-15-8-3-9-16-21/h1,4-5,10-11,19,22H,2-3,6-9,12-17H2\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][C][Branch1][C][C][Branch2][Ring1][Branch1][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring2][Ring1][=Branch1][N]\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H20FNO3/c1-25-18-8-4-16(5-9-18)20(24)22-12-10-15(11-13-22)19(23)14-2-6-17(21)7-3-14/h2-9,15H,10-13H2,1H3\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(COc2ccc(Cc3cnc(N)nc3N)cc2OC)cc1\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n'-(6-chloro-2-methoxyacridin-9-yl)-n,n-diethylpentane-1,4-diamine\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@][Branch1][C][O][Branch2][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][Cl][C][=Branch1][C][=O][N][C][C][C][C][C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1SC(=NC1=O)NC(=O)c2ccccc2\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][N][=C][Branch1][#Branch2][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][C][=C][Branch1][#Branch1][S][C][Ring1][S][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1,3-di(phenyl)propan-1-one\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [1-(4-fluorobenzoyl)piperidin-4-yl]-(4-methoxyphenyl)methanone\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H6O2/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H20N2OS/c21-17(20-14-8-3-1-4-9-14)16-12-7-13-19-18(16)22-15-10-5-2-6-11-15/h2,5-7,10-14H,1,3-4,8-9H2,(H,20,21)\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[5-[(3-dimethylaminobenzoyl)amino]-2-methylphenyl]-3,4-dimethoxybenzamide\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-chloro-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]thiophene-2-sulfonamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C31H39FN4O7/c1-5-42-27(38)11-10-24(16-21-12-13-33-29(21)39)34-30(40)22(15-20-6-8-23(32)9-7-20)17-26(37)28(18(2)3)35-31(41)25-14-19(4)43-36-25/h6-11,14,18,21-22,24,28H,5,12-13,15-17H2,1-4H3,(H,33,39)(H,34,40)(H,35,41)/b11-10+/t21-,22+,24+,28-/m0/s1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1)C2=COc3cc(O)cc(O)c3C2=O\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-phenyl-1,3-benzothiazol-6-ol\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C(Cn1c2CCCCc2c3c(nc(nc13)N4CCCC4)N5CCCC5)N6CCOCC6\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Brc1ccc(cc1)C2NC(=O)c3ccccc3N2\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H14BrN5O4S/c1-11-3-5-14(24(25)26)9-16(11)29(27,28)23-8-7-15(21-23)18-12(2)20-17-6-4-13(19)10-22(17)18/h3-10H,1-2H3\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(N1Cc2ccccc2C1=O)c3ccccc3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-chloro-n-(phenylmethyl)-1,3,5-triazine-2,4-diamine\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H24Cl2N2O/c1-24(21(26)14-16-9-10-18(22)19(23)13-16)20(15-25-11-5-6-12-25)17-7-3-2-4-8-17/h2-4,7-10,13,20H,5-6,11-12,14-15H2,1H3/t20-/m1/s1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H31ClN2O2/c24-21-4-3-18(28-19-2-1-5-25-13-19)9-20(21)22(27)26-14-23-10-15-6-16(11-23)8-17(7-15)12-23/h3-4,9,15-17,19,25H,1-2,5-8,10-14H2,(H,26,27)/t15?,16?,17?,19-,23?/m0/s1\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Cc1cccc2ccccc12)Nc3ccccc3\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COC[C@H](C)Oc1cc(Oc2cc(F)cc(F)c2)cc(c1)C(=O)Nc3ccc(cn3)C(=O)O\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cc(NC(=O)c2oc(Nc3ccccc3F)nn2)ccc1N4CCOCC4\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccccc1CN2C(C(=O)NC3CCC(C)CC3)c4ccccc4C2=O\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[2-hydroxy-5-[(1r)-1-hydroxy-2-[[(2r)-1-(4-methoxyphenyl)propan-2-yl]amino]ethyl]phenyl]formamide\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-(cyclopentylamino)-2-oxo-1-pyridin-4-ylethyl]-n-(furan-2-ylmethyl)-5-phenyl-1h-pyrrole-2-carboxamide\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccc2cccc(O)c2n1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][N][Ring1][=C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H12F4N2OS/c1-7(8-5-3-4-6-9(8)14)18-11-19-10(20)12(2,21-11)13(15,16)17/h3-7H,1-2H3,(H,18,19,20)/t7-,12-/m0/s1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1n[nH]c2c(Cl)cccc12\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][=Branch1][=Branch2][=C][\\\\C][N][=N][NH1][N][=Ring1][Branch1][/C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][N][N][C][=Branch1][C][=O][C][C][C][C][Branch1][C][C][=N][C][=N][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=Ring1][O][C][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2,2-dichloro-n-[(1r,2s)-3-fluoro-1-hydroxy-1-(4-methylsulfonylphenyl)propan-2-yl]acetamide\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-(4-methoxyphenyl)-2-(4-methylpiperazin-1-yl)ethyl]-3-phenylurea\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc2OC(=CC(=O)c2c1)c3ccccc3\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4s)-2-methyl-4-phenyl-3,4-dihydro-1h-isoquinolin-8-amine\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H13N3O2S/c1-15-13(18)16-9-7-10(19-11(9)12(14)17)8-5-3-2-4-6-8/h2-7H,1H3,(H2,14,17)(H2,15,16,18)\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][Branch2][Ring1][=C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][=Branch1][Ring2][=N][Ring1][=Branch2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H17ClN2O3/c1-12-16(11-21(25)26)17-10-14(27-2)4-6-19(17)24(12)20-7-8-23-18-9-13(22)3-5-15(18)20/h3-10H,11H2,1-2H3,(H,25,26)\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-diethylaminoethyl 4-aminobenzoate\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" hovercraft\\n\",\n        \"output\": \" hovercraft is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" impulse\\n\",\n        \"output\": \" impulse is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H9FN2O2/c16-10-1-2-13-11(7-10)12(15(19)20)8-14(18-13)9-3-5-17-6-4-9/h1-8H,(H,19,20)\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1c(C)c2COC(=O)c2c(O)c1C\\\\C=C(/C)\\\\CCC(=O)OCCN3CCOCC3\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" c1ccc2c(c1)nnn2c3ccncc3\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][C][C][C][=Branch1][C][=O][O][C][C][N][C][C][N][Branch2][Ring1][O][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1][C][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(methylsulfanylmethyl)-6-morpholin-4-yl-2-phenylpyrimidine\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)c1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c3ncnc(N)c13\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H35N3O5S/c1-2-3-14-29(23(32)12-17-34-16-11-19-7-5-4-6-8-19)15-13-27-18-22(31)20-9-10-21(30)24-25(20)35-26(33)28-24/h4-10,22,27,30-31H,2-3,11-18H2,1H3,(H,28,33)/t22-/m0/s1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(phenoxy)pyridine-3-carboxamide\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s,3s)-3-[[3,5-bis(trifluoromethyl)phenyl]methoxy]-2-phenylpiperidine\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Ring1][Ring1][N][C][C][=C][C][=N][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O][N][=Ring1][#C]\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" voyage\\n\",\n        \"output\": \" voyage is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(propan-2-ylamino)-3-(2-prop-2-enoxyphenoxy)propan-2-ol\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccccc1CNc2cc(C)ccn2\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[2-[4-[(5-fluoro-1,3-benzodioxol-4-yl)amino]-5-propan-2-yloxyquinazolin-7-yl]oxyethyl]piperazin-1-yl]ethanone\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)C1=Cc2ccc(O)cc2OC1=O\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenoxy)-4-methanesulfonamido-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" discovery\\n\",\n        \"output\": \" discovery is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-[4-(ethyl-heptylamino)-1-hydroxybutyl]phenyl]methanesulfonamide\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19FN4O3/c1-12(25)22-8-16-11-24(19(26)27-16)15-2-3-18(17(20)6-15)23-9-13-4-5-21-7-14(13)10-23/h2-7,16H,8-11H2,1H3,(H,22,25)/t16-/m0/s1\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[[4-(4-chlorophenyl)piperazin-1-yl]methyl]-1-methylbenzimidazole\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][Branch1][=Branch1][C][C][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H8O4/c1-14-12-10-8(4-5-15-10)6-7-2-3-9(13)16-11(7)12/h2-6H,1H3\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][C][C][N][Branch2][Ring1][=Branch1][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(2-methoxyphenyl)methyl]-4-methylpyridin-2-amine\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H29F2N7O3/c28-21-5-1-6-22(26(21)29)32-25(38)13-17-12-24(35-34-17)33-27-20-8-7-19(14-23(20)30-16-31-27)39-11-3-10-36-9-2-4-18(36)15-37/h1,5-8,12,14,16,18,37H,2-4,9-11,13,15H2,(H,32,38)(H2,30,31,33,34,35)/t18-/m1/s1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H24ClFN4O2/c1-29-20-13-19-16(12-21(20)30-10-4-9-28-7-2-3-8-28)22(26-14-25-19)27-15-5-6-18(24)17(23)11-15/h5-6,11-14H,2-4,7-10H2,1H3,(H,25,26,27)\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)Nc1cc(sc1C(=O)N)c2ccsc2\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H11F2N3O2/c1-22-14-9-20-15(12-4-2-3-7-19-12)21-16(14)23-13-6-5-10(17)8-11(13)18/h2-9H,1H3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12N2O2/c1-9-7-14(12(16)13-11(9)15)8-10-5-3-2-4-6-10/h2-7H,8H2,1H3,(H,13,15,16)\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CCN(Cc1ccccc1)c2ccccn2\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1cccc(c1)N2CCN(CCCN3N=C4C=CC=CN4C3=O)CC2\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OCCN1CCN(CCCN2c3ccccc3Sc4ccc(cc24)C(F)(F)F)CC1\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)ethanone\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)C(=O)N(C)C)n2\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C(CN1CCCC1)c2ccccc2)C(=O)Cc3ccc(Cl)c(Cl)c3\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[(4-acetyl-3-hydroxy-2-propylphenoxy)methyl]benzoic acid\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN(C)C4(CCN(C)CC4)C(=O)N\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)C1=CN(Cc2ccc(F)c(F)c2)C(=O)C=C1\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H16N2O2/c22-19(21-14-16-6-4-5-13-20-16)15-9-11-18(12-10-15)23-17-7-2-1-3-8-17/h1-13H,14H2,(H,21,22)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H9NO2/c15-11-7-3-6-9-8-4-1-2-5-10(8)13(16)14(17)12(9)11/h1-7H,15H2\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC1=NN(CC1)c2cccc(c2)C(F)(F)F\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H16ClN/c1-18-10-13-4-2-3-5-15(13)16(11-18)12-6-8-14(17)9-7-12/h2-9,16H,10-11H2,1H3\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nc2ccc(Cl)cc2c3nc(nn13)c4occc4\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cccc(Nc2nc(NCC3CCCO3)c4ccccc4n2)c1\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H29N5O4/c1-31-22-4-2-17-3-5-23(30)29(24(17)27-22)11-10-28-8-6-18(7-9-28)25-15-19-14-20-21(16-26-19)33-13-12-32-20/h2-5,14,16,18,25H,6-13,15H2,1H3\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][Ring1][N]\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H21F2N5O4S/c1-29-13-4-3-12(19)15(20)14(13)16(26)11-9-22-18(24-17(11)21)23-10-5-7-25(8-6-10)30(2,27)28/h3-4,9-10H,5-8H2,1-2H3,(H3,21,22,23,24)\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H11N3O3S/c1-7-6-10(12-16-7)13-17(14,15)9-4-2-8(11)3-5-9/h2-6H,11H2,1H3,(H,12,13)\\n\",\n        \"output\": \" -0.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][S][C][=N][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(carbamoylamino)-5-phenyl-n-[(3s)-piperidin-3-yl]thiophene-2-carboxamide\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H19BrF2N2O3/c1-12-4-5-14(21(28)26-3)9-18(12)27-13(2)8-19(20(23)22(27)29)30-11-15-6-7-16(24)10-17(15)25/h4-10H,11H2,1-3H3,(H,26,28)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)CCOc1ccc(cc1)\\\\C(=C(\\\\Cl)/c2ccccc2)\\\\c3ccccc3\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[(1r)-1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-(1-piperidin-4-ylpyrazol-4-yl)pyridin-2-amine\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H19N3O3S/c1-13-17-14(11-16(18-13)19-7-9-22-10-8-19)12-23(20,21)15-5-3-2-4-6-15/h2-6,11H,7-10,12H2,1H3\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12N2O3/c1-3-14-6-9(12(16)17)10(15)8-5-4-7(2)13-11(8)14/h4-6H,3H2,1-2H3,(H,16,17)\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H21NO2/c1-2-15(18)17-9-7-12-4-3-11-5-6-14-13(16(11)12)8-10-19-14/h5-6,12H,2-4,7-10H2,1H3,(H,17,18)/t12-/m0/s1\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch2][Ring1][Branch2][C][C][N][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][C][Ring1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1C(=O)NCc2cccnc2)C(=O)NCc3cccnc3\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H23F5N6O3S/c23-12-2-1-9(5-13(12)24)11-7-14(11)28-19-16-20(30-21(29-19)37-4-3-22(25,26)27)33(32-31-16)15-6-10(8-34)17(35)18(15)36/h1-2,5,10-11,14-15,17-18,34-36H,3-4,6-8H2,(H,28,29,30)/t10-,11+,14-,15-,17-,18+/m1/s1\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=O]\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H19NO/c1-7-2-8(5-10)4-9(3-7)6-11/h7-9,11H,2-6,10H2,1H3\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(N2CCN(C)CC2)c3nc(cc(N(C)C)c3c1)C(=O)Nc4ccc(cc4)N5CCOCC5\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(8-chloroquinolin-4-yl)-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)c2ccc(NC(=O)c3oc(Nc4ccccc4F)nn3)cn2\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H25N3O2S/c1-18-23(21,22)10-7-13-3-4-17-15(11-13)16(12-19-17)14-5-8-20(2)9-6-14/h3-4,11-12,14,18-19H,5-10H2,1-2H3\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1O[C@]2(CN3CCC2CC3)CN1c4cccs4\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCc1c(C)nc2sc(C(=O)N)c(N)c2c1C\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H20ClN3O4/c22-14-5-6-16-13(7-14)9-17(23-16)20(28)24-18-8-12-3-1-2-4-19(12)25(21(18)29)10-15(27)11-26/h1-7,9,15,18,23,26-27H,8,10-11H2,(H,24,28)/t15-,18?/m1/s1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCNC(=O)c1nnc2c(cccc2c1N)c3ccccc3\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H18ClN3OS/c1-12-18-14(11-22-15-4-2-13(17)3-5-15)10-16(19-12)20-6-8-21-9-7-20/h2-5,10H,6-9,11H2,1H3\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)[N+](C)(CCOC(=O)C1c2ccccc2Oc3ccccc13)C(C)C\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2cccnc2)C(F)(F)F\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccnc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H7N5OS/c16-17(8-4-2-1-3-5-8)10-7-6-9-11-13-14-15(9)12-10/h1-7H\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H27FN2O5/c1-32-18-13-14-21(23(16-18)33-2)29(26(31)22-12-7-15-34-22)24(19-10-5-6-11-20(19)27)25(30)28-17-8-3-4-9-17/h5-7,10-17,24H,3-4,8-9H2,1-2H3,(H,28,30)\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(7-chloroquinolin-4-yl)-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1cc(ncn1)c2ccccc2\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)Cc1ccc(cc1)[C@@H](C)C(=O)NS(=O)(=O)C\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCS(=O)(=O)N1CCCC(C1)C(=O)N2CCC(Cc3ccccc3)CC2\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-n-hydroxy-3-naphthalen-2-yl-2-(naphthalen-2-ylsulfonylamino)propanamide\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][P]\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)C2=Nc3ccccc3Oc4ccc(Cl)cc24\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][C][=C][C][Branch1][#Branch1][O][C][Branch1][C][C][C][=C][C][=Branch1][Ring2][=C][Ring1][#Branch2][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][=C][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][O][=C][Ring1][S]\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][Branch2][Ring1][Ring1][O][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][F][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=C][Ring2][Ring1][P][Ring1][P]\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Oc1ccccc1)N2CCOCC2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(NCCCCc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][=Branch1][Ring1][#C]\\n\",\n        \"output\": \" 3.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][N][=C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][S][Ring1][S]\\n\",\n        \"output\": \" -1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-fluoro-4-morpholin-4-ylphenyl)-5-[(2-fluorophenyl)amino]-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(naphthalen-1-yloxymethyl)-4,5-dihydro-1h-imidazole\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)N1c2ccccc2CC(=O)c3ccccc13\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1C2=Nc3ccccc3CN2c4ccccc14\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 9-(phenylmethyl)purin-6-amine\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(C(=O)c1ccc(F)cc1)c2ccc(F)cc2\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(phenoxymethyl)morpholine\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1cnc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)N5CCNCC5\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C29H35FN4O2/c1-20(2)34(21(3)4)28(35)27(24-14-10-16-31-17-24)25(22-11-6-5-7-12-22)19-33-29(36)32-18-23-13-8-9-15-26(23)30/h5-17,20-21,25,27H,18-19H2,1-4H3,(H2,32,33,36)\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H12N4O4S/c1-20-9-4-2-8(3-5-9)6-13-11(17)15-12-14-7-10(21-12)16(18)19/h2-5,7H,6H2,1H3,(H2,13,14,15,17)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccc2C(=O)C(=O)c3ccccc3c2c1\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-[(1-oxidopyridin-1-ium-3-yl)methylcarbamoylamino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=N][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@@H](Oc1cccc2ncnc(Nc3ccc4c(cnn4Cc5ccccn5)c3)c12)C(=O)N(C)C\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-phenyl-1,2,4-thiadiazol-5-yl)acetamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2nccc(Nc3ccccc3)n2)cc1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H15N3OS/c1-13-9-10-22-16(12-13)20-17(15-8-5-11-24-15)18(22)21-19(23)14-6-3-2-4-7-14/h2-12H,1H3,(H,21,23)\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c(N)c(nc2ccccc12)c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H16ClN3O2S/c1-13-21(28-15-7-5-14(22)6-8-15)20-16(17-11-23-9-10-24-17)3-2-4-18(20)25(13)12-19(26)27/h2-11H,12H2,1H3,(H,26,27)\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1Oc2ccc(cc2)N(Cc3cccnc3)S(=O)(=O)CC(F)(F)F\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-amino-3-(1h-indol-3-yl)propanoic acid\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCn1c2ccccc2c3cc(NC(=O)C(C)C)ccc13\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" aluminum\\n\",\n        \"output\": \" aluminum is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(cc1)C(N2CCNCC2)c3ccccc3\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H22N4O2/c1-25-15-7-4-6-14(12-15)22-20-23-18-10-3-2-9-17(18)19(24-20)21-13-16-8-5-11-26-16/h2-4,6-7,9-10,12,16H,5,8,11,13H2,1H3,(H2,21,22,23,24)\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCC1C(=O)N(N(C1=O)c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-amino-2-(3-fluorophenyl)-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(2s)-1-dimethylamino-1-oxo-3-phenylpropan-2-yl]-5-fluoro-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1)C(=O)Nc2cc(NC(=O)c3cccc(c3)N(C)C)ccc2C\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-3-chloro-2-piperazin-1-ylpyridine-4-carboxamide\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)C2=Cc3ccc(O)cc3OC2=O\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(CN(Cc2ccc(Cl)cc2)c3nn[nH]n3)cc1\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H14ClN3O3/c1-22-14-6-10-12(7-15(14)23-2)18-8-19-16(10)20-9-3-4-11(17)13(21)5-9/h3-8,21H,1-2H3,(H,18,19,20)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H20N2O4S/c26-23(24-27)22(14-16-9-10-17-5-1-3-7-19(17)13-16)25-30(28,29)21-12-11-18-6-2-4-8-20(18)15-21/h1-13,15,22,25,27H,14H2,(H,24,26)/t22-/m1/s1\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)C(=O)C(CCN1CCC(O)(CC1)c2ccc(Cl)cc2)(c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring2][=Branch1][N][C][=Branch1][C][=O][C][=C][Branch1][#Branch1][C][N][Branch1][C][C][C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][N][=C][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][S][Ring1][=N]\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCN(CCO)CCCOc1cc2ncnc(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)c2cc1OC\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H25N3O4S/c1-2-29-22(27)23-16-7-8-20-18(15-16)25(17-5-3-4-6-19(17)30-20)21(26)9-10-24-11-13-28-14-12-24/h3-8,15H,2,9-14H2,1H3,(H,23,27)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1SC(=NC1=O)NC(=O)c2cccc(Cl)c2\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" gorilla\\n\",\n        \"output\": \" gorilla is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)c1cc(C(=O)N2Cc3ccc(CN4CCN(C)CC4)cc3C2)c(O)cc1O\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10O6/c16-8-4-12(19)14-13(5-8)21-6-9(15(14)20)7-1-2-10(17)11(18)3-7/h1-6,16-19H\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-cyclohexyl-1-thiophen-2-ylsulfonylpiperidine-3-carboxamide\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][N][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[2-[(2s)-2-hydroxy-3-propylaminopropoxy]phenyl]-3-phenylpropan-1-one\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(NC(=O)c2ccccc2)n[nH]1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)N1CCN(CC1)c2ccc(OCC3COC(Cn4ccnc4)(O3)c5ccc(Cl)cc5Cl)cc2\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H16BrN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccccc1C(=O)Nc2nc3ccccc3s2\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-hydroxy-3-(4-hydroxyphenyl)chromen-2-one\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)Oc1cc(OCCCN2CCCC2)cc3ncnc(Nc4c(Cl)ccc5OCOc45)c13\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" fall\\n\",\n        \"output\": \" fall is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H16N2O2/c1-3-10-8(6-15-11(10)14)4-9-5-12-7-13(9)2/h5,7-8,10H,3-4,6H2,1-2H3/t8-,10-/m0/s1\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3,3,3-trifluoro-2-hydroxy-n-[4-(4-hydroxyphenyl)sulfonylphenyl]-2-methylpropanamide\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-n'-(5-methyl-1h-pyrazol-3-yl)-6-morpholin-4-ylpyrimidine-2,4-diamine\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Ring1][#Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H](N(c1cc(F)ccc1F)S(=O)(=O)c2ccc(Cl)cc2)c3ccc(F)cc3CCCC(=O)O\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H11FO3/c1-9-13(12(15)6-7-16-9)17-8-10-2-4-11(14)5-3-10/h2-7H,8H2,1H3\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H10N4/c13-12-14-6-5-11(16-12)9-7-15-10-4-2-1-3-8(9)10/h1-7,15H,(H2,13,14,16)\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" caravan\\n\",\n        \"output\": \" caravan is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H27FN4O4S/c1-14(2)12-31-25-22(23(33)29(3)26(31)35)21(24(34)30-9-7-17(32)13-30)20(36-25)10-15-6-8-28-19-5-4-16(27)11-18(15)19/h4-6,8,11,14,17,32H,7,9-10,12-13H2,1-3H3/t17-/m1/s1\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][C][C][C][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc3ccccc3Cl\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-cyclopropyl-5-thiophen-2-yl-1,2-oxazole-3-carboxamide\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[(3,4-dichlorophenyl)methyl]-5-(trifluoromethyl)indole-2-carboxylic acid\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3ccccc3OC\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[4-(diethylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-cyclopropyl-1-methyl-3-oxo-2,1-benzothiazole-5-sulfonamide\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19BrO5/c1-3-4-15-17(8-7-13(11(2)21)18(15)22)25-10-12-5-6-14(19(23)24)16(20)9-12/h5-9,22H,3-4,10H2,1-2H3,(H,23,24)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3cc(F)ccc3F)c2cc1OC\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-[(1r)-2-[2-[3-[2-(3-chlorophenyl)ethylamino]propoxy]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-imidazol-1-yl-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(3r)-3-hydroxypyrrolidine-1-carbonyl]-3-methyl-1-(2-methylpropyl)-6-(quinolin-4-ylmethyl)thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(C)c(c(C)c1)S(=O)(=O)N(C)CCOCC(=O)N2CCN(CC2)C3CCN(C)CC3\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H9NO3/c16-10-6-7-11-12(8-10)14(18)15(13(11)17)9-4-2-1-3-5-9/h1-8,16H\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C@H1][Branch1][C][C][C@H1][Branch1][C][N][C][=N][C@@H1][Branch1][Branch1][C][S][Ring1][Branch1][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][C@H1][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch1][C@@H1][Branch1][C][C][C][C][C][=Branch1][C][=O][N][C@H1][C][C][C][C][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch1][C][C][=Branch1][C][=O][N][N][C][=Branch1][C][=O][C@@H1][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][C][=Branch1][C][=O][C@H1][Branch1][=Branch2][C][C][=C][N][=C][NH1][Ring1][Branch1][N][C][=Branch1][C][=O][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C@@H1][Branch2][Ring1][Ring1][N][C][=Branch1][C][=O][C@@H1][Branch1][Branch1][C][C][C][N][N][C][Ring2][Branch1][Branch2][=O][C@@H1][Branch1][C][C][C][C]\\n\",\n        \"output\": \" -0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-methoxyacridin-9-amine\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)c1ccc(Nc2ncc(Br)c(Nc3ccccc3)n2)cc1\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)c1ccccc1Nc2nc(SCc3cccs3)n[nH]2\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][C][=C][S][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][S]\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H16FN3O/c1-17-4-6-18(7-5-17)14(19)13-9-10-8-11(15)2-3-12(10)16-13/h2-3,8-9,16H,4-7H2,1H3\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][O][C@@H1][Branch1][C][C][C][\\\\C][=C][/C][=Branch1][C][=O][C@@H1][Branch1][C][O][C@@H1][Branch1][C][O][C][\\\\C][=C][\\\\C][Ring2][Ring1][Ring1][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)C1=C(C)NC(=C(C1c2ccccc2[N+](=O)[O-])C(=O)OCC(C)C)C\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H7Cl2FN2O/c13-9-5-7(1-3-10(9)15)12(18)17-8-2-4-11(14)16-6-8/h1-6H,(H,17,18)\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-chloro-2-[[(3s)-3-methyl-4-(2-phenylacetyl)piperazin-1-yl]methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][NH1][C][Branch2][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=Branch1][C][=O][O][=C][Branch1][C][Cl][C][=Ring2][Ring1][#Branch1][Cl]\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H7NO2/c12-9-5-6-10(13)11-8-4-2-1-3-7(8)9/h1-6H,(H,11,13)\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-n'-(3-chlorophenyl)pyridine-3-carbohydrazide\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ncc(c2ccnc(Nc3ccc(cc3)S(=O)(=O)N)n2)n1C\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CO[C@H]1CN(CCCOc2ccc(F)cc2)CC[C@H]1NC(=O)c3cc(Cl)c(N)cc3OC\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n6-[(3,4-dichlorophenyl)methyl]quinazoline-2,4,6-triamine\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C34H41N3O5S/c1-6-8-12-24(7-2)21-35-33(38)26-16-17-30-29(19-26)28(22-37(30)4)18-25-14-15-27(20-31(25)42-5)34(39)36-43(40,41)32-13-10-9-11-23(32)3/h9-11,13-17,19-20,22,24H,6-8,12,18,21H2,1-5H3,(H,35,38)(H,36,39)\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(1h-indol-3-ylsulfanyl)acetic acid\\n\",\n        \"output\": \" -1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(1,3-benzodioxol-5-yl)-5,7-dihydroxychromen-4-one\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-dimethylamino-6-methoxy-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)quinoline-2-carboxamide\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-methyl-4-phenyl-1,3-thiazol-2-amine\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1ccc(cc1)S(=O)(=O)Nc2ccccn2\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2nc(nc(N)c2cc1OC)N3CCN(CC3)C(=O)c4occc4\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H8ClF2NO2S/c13-8-1-4-10(5-2-8)19(17,18)16-12-7-9(14)3-6-11(12)15/h1-7,16H\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C35H46N4O3S/c1-3-39(35(40)28-29-14-16-33(17-15-29)43(2,41)42)32-18-21-36(22-19-32)23-20-34(30-10-6-4-7-11-30)38-26-24-37(25-27-38)31-12-8-5-9-13-31/h4-17,32,34H,3,18-28H2,1-2H3\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Branch1][Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=C][Branch1][=N][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][O][C][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring2][Ring1][Branch2][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=N][C][=Branch1][Branch1][=C][S][Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Br][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 4.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1c(N2CCNC(C)C2)c(F)cc3C(=O)C(=CN(C4CC4)c13)C(=O)O\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ncc2cc(c(N)nc2n1)c3c(Br)cccc3Br\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H25NO2S2/c1-14-7-11-24-18(14)17(19-15(2)8-12-25-19)6-4-10-21-9-3-5-16(13-21)20(22)23/h6-8,11-12,16H,3-5,9-10,13H2,1-2H3,(H,22,23)/t16-/m1/s1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-methyl-5-(piperazin-1-ylmethyl)furan-3-carboxamide\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3occc3\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][N][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][Branch1][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccnc(NCc2ccc(Cl)cc2)c1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-[(3,5-dimethyl-1h-pyrazol-4-yl)methyl]-5-[(4s)-4-hydroxy1,2-oxazolidine-2-carbonyl]-3-methyl-1-(2-methylpropyl)thieno[4,5-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[3-[[2-(3-dimethylaminopropoxy)pyrimidin-4-yl]amino]-4-methylphenyl]-2-morpholin-4-ylpyridine-4-carboxamide\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1c(cnn1c2ccc(F)cc2)C(=O)c3cccc(OC[C@@H](O)CO)c3\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C@@H1][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][=N][C][C][C][N][Branch2][Ring1][P][C][C][C][Branch2][Ring1][Ring1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][O][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-methyl-5-(piperazin-1-ylmethyl)thiophene-3-carboxamide\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch2][Ring1][N][N][C][=Branch1][C][=O][C][C][C][C][Branch1][C][C][=N][C][=N][C][Branch1][C][C][=N][N][Ring1][=Branch1][C][=Ring1][O][C][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-(dimethylaminomethyl)phenyl]sulfanyl-5-methylaniline\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H22O4/c1-3-7-16-17-10-13(2)15(11-14-8-5-4-6-9-14)12-18(17)19(22(25)26)21(24)20(16)23/h4-6,8-10,12,23-24H,3,7,11H2,1-2H3,(H,25,26)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16ClN3O3S/c1-9-5-3-4-6-14(9)20-10(2)19-13-8-12(17)15(24(18,22)23)7-11(13)16(20)21/h3-8,10,19H,1-2H3,(H2,18,22,23)\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][N][S][Ring1][N]\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H14N2O2/c16-15(19)17-12-7-3-1-5-10(12)9-14(18)11-6-2-4-8-13(11)17/h1-8,14,18H,9H2,(H2,16,19)/t14-/m0/s1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(Cc2cnc(N)nc2N)cc(OC)c1OC\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN4CCC[C@@H]4C(=O)N\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H18ClNO2/c1-9-13(16,17-8-12(2,3)15-9)10-5-4-6-11(14)7-10/h4-7,9,15-16H,8H2,1-3H3/t9-,13+/m0/s1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(2-methoxyphenyl)methyl]-n-(4-methylcyclohexyl)-3-oxo-1h-isoindole-1-carboxamide\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)C=C(CCc2cccc(c2)c3ccccc3)N=C1N\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C34H39N3O6S/c1-34(2,36-22-32(40)28-12-15-31(39)30(19-28)37-44(3,42)43)20-24-7-4-6-23(16-24)18-33(41)35-21-25-8-5-9-27(17-25)26-10-13-29(38)14-11-26/h4-17,19,32,36-40H,18,20-22H2,1-3H3,(H,35,41)/t32-/m0/s1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[1-(1-benzothiophen-2-yl)ethyl]-1-hydroxyurea\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H17FN6O3/c19-12-1-3-13(4-2-12)22-18-24-23-17(28-18)16(26)21-14-5-6-15(20-11-14)25-7-9-27-10-8-25/h1-6,11H,7-10H2,(H,21,26)(H,22,24)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-dimethylamino-3-[4-[[4-(phenylamino)pyrimidin-2-yl]amino]phenoxy]propan-2-ol\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H11NO2/c1-3-10(12)11-8-4-6-9(13-2)7-5-8/h3-7H,1H2,2H3,(H,11,12)\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(8-fluoroquinolin-4-yl)-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3cccc(Cl)c3)c2cc1OC\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)C(=O)Oc2ccc(cc2OC(=O)c3ccc(C)cc3)C(O)CNC(C)(C)C\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1OCC(O)COC(=O)N\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-chloro-2-(furan-2-ylmethylamino)-5-sulfamoylbenzoic acid\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H16N2O4S3/c1-3-12-8-4-6(2)18(13,14)10-7(8)5-9(17-10)19(11,15)16/h5-6,8,12H,3-4H2,1-2H3,(H2,11,15,16)/t6-,8-/m0/s1\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(2-fluorophenyl)-1-methyl-7-nitro-3h-1,4-benzodiazepin-2-one\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[4-[bis(2-chloroethyl)amino]phenyl]butanoic acid\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H28ClN3O4S/c23-16-4-1-3-15(13-16)7-9-24-8-2-11-30-12-10-25-14-19(28)17-5-6-18(27)20-21(17)31-22(29)26-20/h1,3-6,13,19,24-25,27-28H,2,7-12,14H2,(H,26,29)/t19-/m0/s1\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" quinazolin-4-amine\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H30FN5O3/c1-30-7-9-32(10-8-30)23-16-18(27)15-21-24(34-2)17-22(29-25(21)23)26(33)28-19-3-5-20(6-4-19)31-11-13-35-14-12-31/h3-6,15-17H,7-14H2,1-2H3,(H,28,33)\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H8N2O3S2/c1-10-7-3-2-5(15(9,12)13)4-6(7)8(11)14-10/h2-4H,1H3,(H2,9,12,13)\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (4-fluorophenyl)-[1-(4-methoxybenzoyl)piperidin-4-yl]methanone\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (e)-n-hydroxy-3-[4-[[2-(2-methyl-1h-indol-3-yl)ethylamino]methyl]phenyl]prop-2-enamide\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 4-[6-(diaminomethylideneamino)hexanoyloxy]benzoate\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(4-methoxyphenyl)methyl]-3-(5-nitro-1,3-thiazol-2-yl)urea\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccccc1OCCNCC(O)COc2cccc3[nH]c4ccccc4c23\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H8N2O3S/c13-9-7-3-1-2-4-8(7)11-10-12(9)5-6-16(10,14)15/h1-4H,5-6H2\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H16ClN3O3/c1-24-15-7-10-14(8-16(15)25-2)21-9-11(18(20)23)17(10)22-13-6-4-3-5-12(13)19/h3-9H,1-2H3,(H2,20,23)(H,21,22)\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][C][C@H1][Branch2][Ring2][Ring2][C][N][C][=Branch2][Ring1][=N][=N][C][=C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][Ring1][=C][C][Ring2][Ring1][C][=O][C][C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C@@H1][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-[(3-methylphenyl)amino]quinazolin-6-yl]prop-2-enamide\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][P][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H24N2O3S/c1-3-21(18-12-6-4-7-13-18)28-26(29)23-20-16-10-11-17-22(20)27-24(25(23)32(2,30)31)19-14-8-5-9-15-19/h4-17,21H,3H2,1-2H3,(H,28,29)/t21-/m0/s1\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][P][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][=N][Ring1][S]\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][Branch1][C][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)S(=O)(=O)c1ccc(NC(=O)C(C)(O)C(F)(F)F)cc1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(6-ethoxy-1,3-benzothiazol-2-yl)propanamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(CS(=O)(=O)c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1C=C(C(=O)O)C(=O)c2cc(F)c(nc12)N3CCNCC3\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(4-methoxyphenyl)-2-[[5-methyl-4-(4-methylphenyl)-1,2,4-triazol-3-yl]sulfanyl]acetamide\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H26N2O7/c1-12(2)30-21(25)18-14(4)22-13(3)17(20(24)29-10-9-28-5)19(18)15-7-6-8-16(11-15)23(26)27/h6-8,11-12,19,22H,9-10H2,1-5H3\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch1][#C][N][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H21ClFN7O/c1-23-18(30)9-15(11-4-6-13(22)7-5-11)25-20-24-10-14(21)19(27-20)26-17-8-16(28-29-17)12-2-3-12/h4-8,10,12,15H,2-3,9H2,1H3,(H,23,30)(H3,24,25,26,27,28,29)/t15-/m0/s1\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5,6-dimethyl-4-(4-pyrimidin-2-ylpiperazin-1-yl)thieno[2,3-d]pyrimidine\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)C(CNC(=O)Nc2ccccc2)N3CCN(C)CC3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch2][Ring1][Ring2][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch1][C][C][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(N1CC(=O)Nc2ccccc12)c3occc3\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H26FN3O6S/c1-13(2)29-21(26)25-9-7-15(8-10-25)30-19-14(3)20(24-12-23-19)31-18-6-5-16(11-17(18)22)32(4,27)28/h5-6,11-13,15H,7-10H2,1-4H3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1,2,3,10-tetramethoxy-9-oxo-6,7-dihydro-5h-benzo[d]heptalen-7-yl)acetamide\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[[(1r,2r)-2-[(2,3-dichloro4h-thieno[2,3-d]pyrrole-5-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]amino]-3-oxopropanoic acid\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][N][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][N][C][=Branch1][=N][=C][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring2][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-morpholin-4-yl-1-phenylethanol\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][C][N][C][C][C][=C][Branch1][C][Cl][C][Branch1][C][O][=C][Branch1][C][O][C][=C][Ring1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)O\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H24Cl2N2O3/c1-15-13-25(14-18-11-20(24)7-4-17(18)12-22(28)29)8-9-26(15)21(27)10-16-2-5-19(23)6-3-16/h2-7,11,15H,8-10,12-14H2,1H3,(H,28,29)/t15-/m0/s1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=C][Branch1][#Branch1][C][=C][Ring1][Branch1][C][=O][C][=Branch1][C][=O][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1onc(c2ccccc2)c1c3ccc(cc3)S(=O)(=O)N\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H5Cl2N3O2/c11-3-1-4(12)6-5(2-3)13-8-7(6)9(16)14-15-10(8)17/h1-2,13H,(H,14,16)(H,15,17)\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ncc(NC(=O)c2cc(NC(=O)c3cccc(c3)C(F)(F)F)ccc2Cl)cc1Cl\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][=C][C][Branch2][Ring1][Branch1][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Ring2][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H27FN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12-\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCC(C)(C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@@H]12\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H19NO5/c1-19-11-14(10-15(19)12-20)17(21)4-2-3-9-24-16-7-5-13(6-8-16)18(22)23/h5-8,10-12H,2-4,9H2,1H3,(H,22,23)\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19FN4/c20-16-3-1-14(2-4-16)18-19(15-5-9-21-10-6-15)24(13-23-18)17-7-11-22-12-8-17/h1-6,9-10,13,17,22H,7-8,11-12H2\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring2][=Branch1][N][C@H1][Branch1][Branch1][S][C][Ring1][=Branch1][C@H1][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C@H1][Branch1][C][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Ring2][Ring1][C][=O][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2,4-diaminopteridin-6-yl)methanol\\n\",\n        \"output\": \" -0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H30N2O2/c1-3-5-12-20(13-6-4-2)14-7-15-22-18(21)16-8-10-17(19)11-9-16/h8-11H,3-7,12-15,19H2,1-2H3\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1CS(=O)(=O)CC1N2CCC(CC2)c3ccccc3\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[3-(difluoromethyl)-5-(3-fluoro-4-methoxyphenyl)pyrazol-1-yl]benzenesulfonamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][P][O][C][=Branch1][C][=O][C][C][C][C][C][N][=C][Branch1][C][N][N][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(C1CCN(CCC(C2CCN(Cc3ccccc3)CC2)c4ccccc4)CC1)C(=O)Cc5ccc(cc5)S(=O)(=O)C\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" plywood\\n\",\n        \"output\": \" plywood is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][C][N][C][Branch1][=Branch2][N][S][Ring1][=Branch1][=Branch1][C][=O][=O][C][Branch1][C][Cl][Cl][C][=C][Ring1][#C][Cl]\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C37H37F2N3O4S/c1-22(2)35(44)40-26-16-14-25(15-17-26)34-28(19-41(5)18-24-10-7-6-8-11-24)32-33(43)29(37(45)46-23(3)4)21-42(36(32)47-34)20-27-30(38)12-9-13-31(27)39/h6-17,21-23H,18-20H2,1-5H3,(H,40,44)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H19N3O/c1-14-6-2-3-7-15(14)17(21)20-12-10-19(11-13-20)16-8-4-5-9-18-16/h2-9H,10-13H2,1H3\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H12F3N5/c12-11(13,14)10-16-15-8-4-5-9(17-19(8)10)18-6-2-1-3-7-18/h4-5H,1-3,6-7H2\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-methoxyphenyl)-3-(2,5,7-trimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)propanamide\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H20N2O/c1-2-19-14-9-7-13(8-10-14)15-12-17-16-6-4-3-5-11-18(15)16/h7-10,12H,2-6,11H2,1H3\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1C(=O)CN=C(c2ccccc2)c3cc(Cl)ccc13\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H22N6O/c1-12(2)25-13(3)22-11-17(25)16-9-10-21-19(24-16)23-15-7-5-14(6-8-15)18(26)20-4/h5-12H,1-4H3,(H,20,26)(H,21,23,24)\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)Nc1cc(sc1C(=O)N[C@H]2CCCNC2)c3ccccc3\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][S][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][C][O][Ring1][Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(9,10-dioxophenanthren-2-yl)-2,2-dimethylpropanamide\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][N][C][=N][C][=N][Ring1][Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=Branch2][Ring2][#Branch2][=N][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][=C][C][=Branch1][=Branch2][=N][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [(2r)-1-[4-[(4-fluoro-2-methyl-1h-indol-5-yl)oxy]-5-methylpyrrolo[5,1-f][1,2,4]triazin-6-yl]oxypropan-2-yl] (2s)-2-aminopropanoate\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC(=O)c1cc(sc1NC(=O)N)c2ccccc2\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1C(=O)CC(C1=O)c2ccccc2\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][N][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[4-[[4-[(3-chlorophenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H9Cl2N3O/c11-6-2-1-5(3-7(6)12)8-4-9(16)15-10(13)14-8/h1-3,8H,4H2,(H3,13,14,15,16)\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H12O2/c15-14(12-7-3-1-4-8-12)11-16-13-9-5-2-6-10-13/h1-10H,11H2\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Branch1][Ring2][N][=Ring1][#C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" stone\\n\",\n        \"output\": \" stone is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cccc([C@H](O)C2CCN(CCc3ccc(F)cc3)CC2)c1OC\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-methyl-n-[3-[[[2-[(2-oxo-1,3-dihydroindol-5-yl)amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]methyl]pyridin-2-yl]methanesulfonamide\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H14N4/c1-2-6-12-11(5-1)17-15(18-12)9-10-16-19-13-7-3-4-8-14(13)20-16/h1-8H,9-10H2,(H,17,18)(H,19,20)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H34N4O2/c1-31-23-12-6-5-11-22(23)28-18-15-27(16-19-28)17-20-29(24-13-7-8-14-26-24)25(30)21-9-3-2-4-10-21/h5-8,11-14,21H,2-4,9-10,15-20H2,1H3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(OC2CCN(C)CC2)c3c(Nc4cccc5OCOc45)ncnc3c1\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" FC(F)(F)c1nnc2ccc(nn12)N3CCCCCC3\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc(cc1)S(=O)(=O)c2ccc(N)cc2\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][=Branch1][C][C][N][Ring1][=Branch1][O][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H19ClN4O/c1-15(2,3)12-9-13(20(4)19-12)18-14(21)17-11-7-5-10(16)6-8-11/h5-9H,1-4H3,(H2,17,18,21)\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H22ClN5O/c20-16-5-3-6-17(15-16)23-13-11-22(12-14-23)8-4-10-25-19(26)24-9-2-1-7-18(24)21-25/h1-3,5-7,9,15H,4,8,10-14H2\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H36N6O/c1-2-8-20-19(7-1)21-22(28-9-3-4-10-28)25-24(29-11-5-6-12-29)26-23(21)30(20)14-13-27-15-17-31-18-16-27/h1-18H2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C7H6N2/c1-2-4-7-6(3-1)5-8-9-7/h1-5H,(H,8,9)\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-carbamimidoyl-n-(4-ethylphenyl)naphthalene-2-carboxamide\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC(=O)c1ccc(Nc2nccc(n2)c3cnc(C)n3C(C)C)cc1F\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4-chlorophenyl)-[1-(4-fluorobenzoyl)piperidin-4-yl]methanone\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" fedelini\\n\",\n        \"output\": \" fedelini is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)C1=CN(Cc2ccccc2)C(=O)N(Cc3ccc(F)cc3)C1=O\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC1=NC(CC(=O)N1)c2ccc(Cl)c(Cl)c2\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-n-[1-[2-(2-hydroxyethylamino)-2-oxoethyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-chloro-2-fluorophenyl)-6-methoxy-7-[2-(1,2,4-triazol-1-yl)ethoxy]quinazolin-4-amine\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-acetyl-7-diethylaminochromen-2-one\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-methyl-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(4-amino-2-butylimidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H14N2O2/c14-11(13-6-8-15-9-7-13)12-10-4-2-1-3-5-10/h1-5H,6-9H2,(H,12,14)\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5z)-5-[(3,4-dimethoxyphenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one\\n5-[(3,4-dimethoxyphenyl)methylidene]-2-sulfanylidene-1,3-thiazolidin-4-one\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,1-dioxo-2,3-dihydro-[1,3]thiazolo[2,3-b]quinazolin-5-one\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H23ClN4O4S/c24-19-11-14-10-16(26-22(14)33-19)21(31)25-17-9-13-3-1-2-4-18(13)28(23(17)32)12-20(30)27-7-5-15(29)6-8-27/h1-4,10-11,15,17,26,29H,5-9,12H2,(H,25,31)\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H20N2O5S/c1-2-3-9-19-14-10-12(17(20)21)11-15(25(18,22)23)16(14)24-13-7-5-4-6-8-13/h4-8,10-11,19H,2-3,9H2,1H3,(H,20,21)(H2,18,22,23)\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C(C(C1CCCCC1)C2CCCCC2)C3CCCCN3\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-cyclopropyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H16ClNO4S2/c1-11-18(25-13-5-3-12(19)4-6-13)15-9-14(26(2,23)24)7-8-16(15)20(11)10-17(21)22/h3-9H,10H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-aminophenyl)-4-[3-chloro-5-[(4-ethylpiperazin-1-yl)methyl]pyridin-2-yl]benzamide\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c(c(nc2ccccc12)c3ccccc3)S(=O)(=O)C)c4ccccc4\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][Branch1][P][N][=C][Ring1][=Branch1][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1)C2=C(C)c3ccc(OC)cc3OC2=O\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H14O3/c17-15(10-11-16(18)19)14-8-6-13(7-9-14)12-4-2-1-3-5-12/h1-9H,10-11H2,(H,18,19)\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccccc1C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H26F3N5O5/c25-24(26,27)37-17-2-4-19-18(11-17)32(22(34)14-36-19)10-9-31-7-5-15(6-8-31)28-12-16-1-3-20-23(29-16)30-21(33)13-35-20/h1-4,11,15,28H,5-10,12-14H2,(H,29,30,33)\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@]12CC[C@H]3[C@@H](CC(=C)C4=CC(=O)C=C[C@]34C)[C@@H]1CCC2=O\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-butyl-3-[[4-[2-(2h-tetrazol-5-yl)phenyl]phenyl]methyl]-1,3-diazaspiro[4.4]non-1-en-4-one\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1c(c2cc(F)ccc2n1CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H10ClN3OS2/c1-2-13-10-14-9(12)8(17-10)7(15)5-3-4-6(11)16-5/h3-4H,2,12H2,1H3,(H,13,14)\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][C][C@H1][C@@H1][C][C][C@H1][Branch1][=Branch1][C][=Branch1][C][=O][C][C@@][Ring1][Branch2][Branch1][C][C][C][C@H1][Branch1][C][O][C@@H1][Ring1][=C][C@@][Branch1][C][C][C][C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][Branch2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-(2,3-dichlorophenyl)-1,2,4-triazine-3,5-diamine\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H26N2O2S/c1-3-22(19-13-7-5-8-14-19)29-27(30)24-21-17-11-12-18-23(21)28-25(26(24)32(31)4-2)20-15-9-6-10-16-20/h5-18,22H,3-4H2,1-2H3,(H,29,30)/t22-,32?/m0/s1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][\\\\C][=Branch1][=N][=C][Branch1][C][\\\\Cl][/C][=C][C][=C][C][=C][Ring1][=Branch1][\\\\C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2-(4-chlorophenyl)-6,6-dimethyl-1-phenyl-5,7-dihydropyrrolizin-3-yl]acetic acid\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(F)c(NS(=O)(=O)c2ccc(Cl)cc2)c1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][P][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][Branch1][C][C][=N][C][Branch1][C][C][=C][Ring1][Branch2][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H16N6O2S/c1-10-18-9-14(21(10)2)13-7-8-17-15(20-13)19-11-3-5-12(6-4-11)24(16,22)23/h3-9H,1-2H3,(H2,16,22,23)(H,17,19,20)\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-phenylpyrimidin-2-amine\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (4-methylphenyl)methyl 4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5-chloro-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(1,3-thiazol-4-yl)-1h-benzimidazole\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Branch1][C][Cl][C][=C][C][Ring2][Ring1][Branch1][=N][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1sc(N)nc1c2ccccc2\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cc(F)cc(F)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(4-chlorophenyl)-2-(2-imino-3-methylbenzimidazol-1-yl)ethanone\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(7-oxo-6h-[1,3]thiazolo[5,4-d]pyrimidin-2-yl)benzamide\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H13BN2O3S/c1-11-6-8-13(9-7-11)21(19,20)17-15(18)14-5-3-2-4-12(14)10-16-17/h2-10,18H,1H3\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H10N2OS/c12-10(14)8-6-9(15-11(8)13)7-4-2-1-3-5-7/h1-6H,13H2,(H2,12,14)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch2][Ring2][=Branch1][N][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch1][C][=C][Ring2][Ring1][=N][C][=C][Ring2][Ring1][P][O][C][C][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H22N2O2/c1-23-19-8-7-14(11-20(19)24-2)12-22-10-9-16-15-5-3-4-6-17(15)21-18(16)13-22/h3-8,11,21H,9-10,12-13H2,1-2H3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][N][=C][N][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch1][N][Ring1][=Branch1][N][=Ring1][=Branch2][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,3-dihydroxyxanthen-9-one\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][C][=N][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][C][C@@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(C)c(C(=O)N[C@@H](Cc2ccc(OCCCNc3ccccn3)cc2)C(=O)O)c(C)c1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-[4-[(4-chlorophenyl)-phenylmethyl]piperazin-1-yl]ethoxy]acetic acid\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][Branch2][C][C][Branch1][C][O][C][O][C][=Ring1][#Branch2][C][Ring1][S][=O]\\n\",\n        \"output\": \" -1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][C][N][Branch2][Ring1][Ring1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][C][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][C][C][=C][C][=C][C][N][C][=Branch1][C][=O][C][C][Ring1][#Branch2][=Ring1][=Branch1]\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C29H30F3N3O7/c1-17(2)25(26(37)29(30,31)32)34-24(36)15-35-23(19-12-20(40-3)14-21(13-19)41-4)11-10-22(27(35)38)33-28(39)42-16-18-8-6-5-7-9-18/h5-14,17,25H,15-16H2,1-4H3,(H,33,39)(H,34,36)\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-naphthalen-1-yl-3a,4,5,9b-tetrahydro-3h-cyclopenta[c]quinoline-8-sulfonamide\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCCC1=NC2(CCCC2)C(=O)N1Cc3ccc(cc3)c4ccccc4c5nn[nH]n5\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-methyl-1h-quinolin-2-one\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-n-[(4-chlorophenyl)methyl]-1-(7h-pyrrolo[3,2-e]pyrimidin-4-yl)piperidine-4-carboxamide\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(ccc1Cn2ncc3ccc(NC(=O)OC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[1-[3,3-di(phenyl)propyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)-n-prop-2-enylacetamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=S(=O)(Nc1cccnc1)c2ccc3OCCOc3c2\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][Branch2][Ring1][#Branch1][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][C][=C][C][=C][C][=C][Ring2][Ring1][#Branch1][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H22ClFN4O2/c1-27-8-6-13(7-9-27)29-19-10-14-17(11-18(19)28-2)24-12-25-21(14)26-16-5-3-4-15(22)20(16)23/h3-5,10-13H,6-9H2,1-2H3,(H,24,25,26)\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C30H29N3O4/c1-33(28-13-7-8-18-31-28)19-20-37-24-16-14-22(15-17-24)21-27(30(35)36)32-26-12-6-5-11-25(26)29(34)23-9-3-2-4-10-23/h2-18,27,32H,19-21H2,1H3,(H,35,36)/t27-/m0/s1\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][N][=Ring1][N]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H26Cl2N4O2/c1-2-22-9-10-26-15(12-22)13-23-5-7-24(8-6-23)18(25)21-14-3-4-16(19)17(20)11-14/h3-4,11,15H,2,5-10,12-13H2,1H3,(H,21,25)/t15-/m1/s1\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H25ClN2O3/c22-19-8-6-18(7-9-19)21(17-4-2-1-3-5-17)24-12-10-23(11-13-24)14-15-27-16-20(25)26/h1-9,21H,10-16H2,(H,25,26)\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3CCN(CC3)c4cnccn4)c(F)c2\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(CN1C(=O)NC2=C(C=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C2=O)c3ccccc3)C1=O)OC\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27N5O5/c29-17-2-4-19-18(11-17)28(22(31)14-33-19)10-9-27-7-5-15(6-8-27)24-12-16-1-3-20-23(25-16)26-21(30)13-32-20/h1-4,11,15,24,29H,5-10,12-14H2,(H,25,26,30)\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2-[1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=Branch1][Ring2][=C][Ring1][#Branch1][N][C][=Branch2][Ring1][O][=C][C][=Branch1][=Branch2][=C][Branch1][C][Br][C][Ring1][#Branch1][=O][O][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][Branch2][C][C][C][N][Branch2][Ring1][N][C][C][C][Branch1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][Branch2][Ring1][P][C][C][=C][C][Branch1][C][I][=C][Branch1][S][O][C][=C][C][=C][Branch1][C][O][C][Branch1][C][I][=C][Ring1][Branch2][C][Branch1][C][I][=C][Ring1][P][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-dimethylamino-n-pyrazin-2-ylnaphthalene-1-sulfonamide\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Branch2][Ring1][C][N][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][N][=C][Ring2][Ring1][=Branch1][Ring1][P]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCO[C@@H]1OC(=O)C[C@@H]1NC(=O)[C@@H]2CCCN3N2C(=O)[C@H](CCC3=O)NC(=O)c4nccc5ccccc45\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H5ClF9N3O/c15-11-25-4-8(9(27-11)14(22,23)24)10(28)26-7-2-5(12(16,17)18)1-6(3-7)13(19,20)21/h1-4H,(H,26,28)\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-phenylquinolin-4-amine\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(cc(OC)c1OC)C(=O)NCc2ccc(OCCN(C)C)cc2\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" partner\\n\",\n        \"output\": \" partner is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-nitrophenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-hydroxybenzoic acid\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=C][C][=Branch1][=Branch1][=C][C][=N][Ring1][=Branch1][C][=Branch1][C][=S][N]\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1onc(C(=O)N)c1C(=O)Nc2nccs2\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCNc1nc(N)c(s1)C(=O)c2ccc(Cl)s2\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch2][Ring2][Ring1][C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][N][Ring2][Ring1][N][C]\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H24FN3O4/c1-29-20-17-13(19(26)14(21(27)28)9-25(17)12-4-5-12)7-15(22)18(20)24-8-11-3-2-6-23-16(11)10-24/h7,9,11-12,16,23H,2-6,8,10H2,1H3,(H,27,28)/t11-,16+/m0/s1\\n\",\n        \"output\": \" -0.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" behavior\\n\",\n        \"output\": \" behavior is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" friend\\n\",\n        \"output\": \" friend is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-dimethylamino-n-[3-[(4-hydroxybenzoyl)amino]-4-methylphenyl]benzamide\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1C(=O)Cc3cccc(Cl)c3\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[5-(4-methylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonamide\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cccc(n1)c2nn3CCCc3c2c4ccnc5ccc(cc45)C(=O)N\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2nc(NC(=O)CCc3ccc(OC)c(OC)c3)sc2c1\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" [O-][N+](=O)c1cccc2C(=O)C(=O)c3ccccc3c12\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][S][C][Branch1][#Branch2][C][N][C][C][N][C][C][Ring1][=Branch1][=C][C][=Ring1][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCc1cccc(CC)c1NC(=O)N2Cc3[nH]nc(NC(=O)c4ccc(cc4)N5CCN(C)CC5)c3C2\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21N5O2/c1-22-9-11-23(12-10-22)13-17(25)24-16-7-3-2-5-14(16)19(26)21-15-6-4-8-20-18(15)24/h2-8H,9-13H2,1H3,(H,21,26)\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(4-imidazo[2,3-f]pyridazin-3-ylpyrimidin-2-yl)amino]-n-(2-methoxyethyl)benzenesulfonamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[[(5s)-3-[3-fluoro-4-(4-pyrazin-2-ylpiperazin-1-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccnc(CSc2nc3ccccc3[nH]2)c1\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidine-1-carbonyl]-2h-isoquinolin-1-one\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[1-[3,3-di(phenyl)propyl]piperidin-4-yl]-n-methylpyridine-4-carboxamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccc(OCc2ccccc2)cc1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H22N4O4S/c1-14-10-15(2)12-16(11-14)19-22-23-21(29-19)30-13-18(26)24-5-7-25(8-6-24)20(27)17-4-3-9-28-17/h3-4,9-12H,5-8,13H2,1-2H3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H17NO3/c1-19(2,3)18(23)20-11-8-9-13-12-6-4-5-7-14(12)16(21)17(22)15(13)10-11/h4-10H,1-3H3,(H,20,23)\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cn1c(CN2CCN(CC2)c3ccc(Cl)cc3)nc4ccccc14\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N+1][Branch1][C][C][Branch2][Ring1][N][C][C][O][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-piperazin-1-ylbenzamide\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-phenyl-1,2-benzoselenazol-3-one\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(4-methoxyphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H11NO3/c1-5-8(12)7(4-11)6(3-10)2-9-5/h2,10-12H,3-4H2,1H3\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(N2CCN(C)CC2)c3NC(=CC(=O)c3c1)C(=O)Nc4ccc(cc4)N5CCOCC5\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-[carbamoyl-(2,6-difluorophenyl)amino]-2-(2,4-difluorophenyl)pyridine-3-carboxamide\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](CO)Nc1nc(SCc2ccccc2)nc3nc(N)sc13\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@](O)(C(=O)Nc1ccc(cc1Cl)C(=O)N2CCCCC2)C(F)(F)F\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H15NO3/c14-12(13-6-8-15-9-7-13)10-16-11-4-2-1-3-5-11/h1-5H,6-10H2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC4CCN(CC4)S(=O)(=O)C\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H20N4O3S/c1-11(2)18-16(21)20-24(22,23)15-10-17-8-7-14(15)19-13-6-4-5-12(3)9-13/h4-11H,1-3H3,(H,17,19)(H2,18,20,21)\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H27ClN8O2/c1-32-8-10-33(11-9-32)12-13-34-24-21-22(27-16-28-23(21)30-31-24)29-17-5-6-20(19(25)14-17)35-15-18-4-2-3-7-26-18/h2-7,14,16H,8-13,15H2,1H3,(H2,27,28,29,30,31)\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc2ccccc2s1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)NCc1ccc(CN2CCN(CC2)c3ccc(F)cc3F)cc1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C@H1][Branch1][P][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H20N6O2/c1-13(2)23-16-4-3-15-9-22-26(17(15)8-16)19-11-21-10-18(24-19)25-6-5-14(12-25)7-20(27)28/h3-6,8-13,23H,7H2,1-2H3,(H,27,28)\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-methyl-5-[3-(quinolin-2-ylmethoxy)phenyl]pentanoic acid\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H24N4O/c1-4-5-10-14-21-15-16(22(14)11-18(2,3)23)12-8-6-7-9-13(12)20-17(15)19/h6-9,23H,4-5,10-11H2,1-3H3,(H2,19,20)\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H11NO/c14-12(10-5-2-1-3-6-10)11-7-4-8-13-9-11/h1-9,12,14H\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[2,6-di(morpholin-4-yl)pyrimidin-4-yl]-4-(trifluoromethyl)pyridin-2-amine\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" chicory\\n\",\n        \"output\": \" chicory is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H15BrN2O2S/c14-10-1-2-11(19-10)16-8-13(18-12(16)17)7-15-5-3-9(13)4-6-15/h1-2,9H,3-8H2/t13-/m1/s1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][=C][N][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@](Cc1ccc(O)c(O)c1)(NN)C(=O)O\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(5-amino-6-oxo-2-thiophen-2-ylpyrimidin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H16F2N6O3/c19-13-3-1-11(9-14(13)20)23-18-25-24-17(29-18)16(27)22-12-2-4-15(21-10-12)26-5-7-28-8-6-26/h1-4,9-10H,5-8H2,(H,22,27)(H,23,25)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[[(2s)-azetidin-2-yl]methoxy]-2-fluoropyridine\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC[C@H](C)Oc1cc(O[C@@H](C)Cc2ccccc2)cc(c1)C(=O)Nc3ccc(cn3)C(=O)O\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch1][C][C][=C][C][Branch2][Ring1][P][N][C@H1][C][C][C][C@@H1][Branch1][Ring2][C][Ring1][=Branch1][N][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][O][=N][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CS(=O)(=O)Cc1cc(nc(n1)c2ccc3[nH]ccc3c2)N4CCOCC4\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=C][N][=C][Branch1][Ring1][C][O][C][=N][C][Ring1][Branch2][=N][Ring1][=N]\\n\",\n        \"output\": \" -0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H20N2O3/c1-12-16-8-9-22(13-4-6-14(23)7-5-13)20(16)17-10-15(24-2)11-18(25-3)19(17)21-12/h4-7,10-11,23H,8-9H2,1-3H3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3\\n\",\n        \"output\": \" -0.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H20N6O4/c1-27-15-4-2-3-13(11-15)22-19-24-23-18(29-19)17(26)21-14-5-6-16(20-12-14)25-7-9-28-10-8-25/h2-6,11-12H,7-10H2,1H3,(H,21,26)(H,22,24)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCC(N(CCCN)C(=O)c1ccc(C)cc1)C2=Nc3snc(C)c3C(=O)N2Cc4ccccc4\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCNC(=O)c1nnc2c(cccc2c1N)c3cnccc3OC\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(2s)-1-dimethylamino-1-oxo-3-phenylpropan-2-yl]-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H10ClNO2/c14-9-6-7-12(16)11(8-9)13(17)15-10-4-2-1-3-5-10/h1-8,16H,(H,15,17)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H21FN2O3S/c1-14-4-6-15(7-5-14)13-21-19(23)18-3-2-12-22(18)26(24,25)17-10-8-16(20)9-11-17/h4-11,18H,2-3,12-13H2,1H3,(H,21,23)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)c1ccccc1c2ccc(Cl)c(c2)C(=O)NCC3(O)CCCCCC3\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-chloro-1-(4-hydroxyphenyl)-2,3,4,5-tetrahydro-1h-3-benzazepine-7,8-diol\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][=C][Ring1][=N]\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-amino-8-[5-(azetidine-1-carbonyl)pyridin-3-yl]-n-propylcinnoline-3-carboxamide\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1C[C@@H](c2ccccc2)c3cccc(N)c3C1\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H10N2S/c1-3-7-11(8-4-1)13-15-16-14(17-13)12-9-5-2-6-10-12/h1-10H\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C(=O)O)c1cccc(c1)C(=O)c2ccccc2\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNc1ccc(cc1)c2nc3ccc(O)cc3s2\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][Branch2][Ring2][=C][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][#Branch2][N][C][=C][C][=C][C][Branch1][#C][C][=N][N][Ring1][Branch1][C][C][=C][C][=C][C][=N][Ring1][=Branch1][=C][Ring1][S][=C][Ring2][Ring1][O][Ring2][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" piperidin-1-yl-(4,5,6,7-tetrahydro-2-benzothiophen-1-yl)methanone\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCn1c2ccccc2c3cc(NC(=O)C)ccc13\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" half-sister\\n\",\n        \"output\": \" half-sister is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(NCc1ccccn1)c2ccc(Oc3ccccc3)cc2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][=C][Branch1][C][N][N][Branch1][Ring2][N][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C=CNC1=S\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-methoxyphenyl)-2-phenyl-1,2,4-thiadiazol-2-ium-5-amine\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" felony\\n\",\n        \"output\": \" felony is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H32N4O/c1-19-6-2-3-7-20(19)18-27-14-10-21(11-15-27)28-16-12-22(13-17-28)29-24-9-5-4-8-23(24)26-25(29)30/h2-9,21-22H,10-18H2,1H3,(H,26,30)\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H10ClNO2/c16-11-7-5-10(6-8-11)9-17-13-4-2-1-3-12(13)14(18)15(17)19/h1-8H,9H2\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H20N2OS/c21-18(19-15-12-20-10-8-13(15)9-11-20)17-7-6-16(22-17)14-4-2-1-3-5-14/h1-7,13,15H,8-12H2,(H,19,21)/t15-/m0/s1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][N][C][=N][C][=N][C][=C][C][Branch1][O][O][C][C][N][C][C][C][C][Ring1][Branch1][=C][C][Branch1][#Branch2][O][C][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C@H1][Branch2][Ring2][C][C@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2][C][=Branch1][C][=O][N][C][C@@H1][Branch1][C][O][C@@H1][Branch1][C][O][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1cc(ccc1C2=CCOCC2)N3C[C@H](COc4ccon4)OC3=O\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-hydroxybenzamide\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-piperidin-1-ylpropoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" pyridin-2-ylmethyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamate\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H31Cl2N3O4S/c1-18-3-6-22(7-4-18)35(32,33)28(2)25(31)30-13-9-19(10-14-30)29-15-11-20(12-16-29)34-21-5-8-23(26)24(27)17-21/h3-8,17,19-20H,9-16H2,1-2H3\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][O][C][=Branch1][N][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][Ring1][O][=O]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H21NO3S/c1-10(2)9-12-5-7-13(8-6-12)11(3)14(16)15-19(4,17)18/h5-8,10-11H,9H2,1-4H3,(H,15,16)\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=N][C][Branch1][C][Br][=C][N][=C][Ring1][#Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H17N5/c1-9-3-4-11-12(7-9)19-10(2)8-17-14(19)13(18-11)16-6-5-15/h3-4,7-8H,5-6,15H2,1-2H3,(H,16,18)\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][N][C][=C][C][=Branch2][Ring1][=Branch2][=C][C][=Branch1][=N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H19F3N2S/c1-22(2)10-5-11-23-14-6-3-4-7-16(14)24-17-9-8-13(12-15(17)23)18(19,20)21/h3-4,6-9,12H,5,10-11H2,1-2H3\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C@H1][Branch2][Ring1][Branch2][C][N][C][=Branch1][C][=O][C][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H20ClN3O3S2/c1-4-20(5-2)15(21)9-12-10-24-16(18-12)19-25(22,23)14-8-6-7-13(17)11(14)3/h6-8,10H,4-5,9H2,1-3H3,(H,18,19)\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H27ClO5S/c1-3-6-17-20(9-8-16(23(17)28)19(25)4-2)29-11-5-12-30-21-10-7-15(13-18(21)24)14-22(26)27/h7-10,13,28H,3-6,11-12,14H2,1-2H3,(H,26,27)\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-amino-4,6-dimethyl-n-(phenylmethyl)thieno[5,4-b]pyridine-2-carboxamide\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-(2-hydroxy-3-propylaminopropoxy)phenyl]-3-phenylpropan-1-one\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][N][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccccc1NC(=O)CCS(=O)(=O)c2ccc(Br)s2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H7ClN2O2S/c1-5-10-7-3-2-6(9)4-8(7)14(12,13)11-5/h2-4H,1H3,(H,10,11)\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H22FN9O/c1-11-7-15(27-26-11)23-14-8-16(28-3-5-29-6-4-28)25-18(24-14)22-12(2)17-20-9-13(19)10-21-17/h7-10,12H,3-6H2,1-2H3,(H3,22,23,24,25,26,27)/t12-/m0/s1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H14Cl2N2O3S/c19-15-16-13(26-17(15)20)7-12(21-16)18(25)22-11-5-8-3-1-2-4-9(8)10(11)6-14(23)24/h1-4,7,10-11,21H,5-6H2,(H,22,25)(H,23,24)/t10-,11-/m1/s1\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(4-methylsulfonylphenoxy)-5-propan-2-yloxy-n-(1,3-thiazol-2-yl)benzamide\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-n-[(2r)-1-[[(1r)-1-formamido-2-(1h-indol-3-yl)ethyl]amino]-3-(1h-indol-3-yl)-1-oxopropan-2-yl]-2-methylpropanamide\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H23ClN2/c1-21-12-5-13-22(15-14-21)19(16-6-3-2-4-7-16)17-8-10-18(20)11-9-17/h2-4,6-11,19H,5,12-15H2,1H3\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN2CCC3(CC2)Cc4cc(F)ccc4O3\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(5-methyl-1,3-thiazol-2-yl)-2-phenylacetamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(c1ccc2c(C)n(C)nc2c1)c3ccnc(Nc4ccc(C)c(c4)S(=O)(=O)N)n3\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(=O)c1ccc(cc1)C2=CC3(CCNCC3)Oc4cccc(O)c24\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1c2CCN(c3ccccc3)c2nc4ccc(Br)cc14\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H29N3O4/c1-18-8-11-21(27-26(31)20-6-5-7-22(16-20)29(2)3)17-24(18)28-25(30)19-9-12-23(13-10-19)33-15-14-32-4/h5-13,16-17H,14-15H2,1-4H3,(H,27,31)(H,28,30)\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-amino-5-ethyl-4,6-dimethylthieno[4,5-e]pyridine-2-carboxamide\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (r)-(2,3-dimethoxyphenyl)-[1-[2-(4-fluorophenyl)ethyl]piperidin-4-yl]methanol\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][=C][Ring1][=C][N][=C][N][Ring1][Branch1][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O]\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1ccccc1OCc2ccccc2\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-oxo-6h-benzo[b][1]benzazepine-11-carboxamide\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[1-[[4-(6-methyl-5-oxo-3-phenyl-4h-pyrazin-2-yl)phenyl]methyl]piperidin-4-yl]-1h-benzimidazol-2-one\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-ethyl-n-[1-[(3s)-3-(4-fluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H28ClNO/c1-3-28(4-2)19-20-29-24-17-15-22(16-18-24)25(21-11-7-5-8-12-21)26(27)23-13-9-6-10-14-23/h5-18H,3-4,19-20H2,1-2H3/b26-25+\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)CCn1c2ccccc2c3ccccc13\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)c1noc(C)c1C(=O)Nc2nccs2\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H31N5O2S/c1-4-22(31(16-8-15-28)26(33)21-13-11-18(2)12-14-21)24-29-25-23(19(3)30-35-25)27(34)32(24)17-20-9-6-5-7-10-20/h5-7,9-14,22H,4,8,15-17,28H2,1-3H3\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C][N][C][C][N][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][C][=C][C][Ring2][Ring1][Ring2][=N][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C@H1][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][Cl][C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" deer\\n\",\n        \"output\": \" deer is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H21N5O3/c1-28-19-9-15-18(10-20(19)29-2)24-13-25-22(15)27-8-7-14(12-27)30-21-11-23-16-5-3-4-6-17(16)26-21/h3-6,9-11,13-14H,7-8,12H2,1-2H3/t14-/m1/s1\\n\",\n        \"output\": \" 4.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1C=COc2ccccc12\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][Branch2][Ring1][N][C][Branch1][#Branch2][C][N][C][C][O][C][C][Ring1][=Branch1][=N][N][Ring1][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(benzotriazol-1-ylmethyl)-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazin-6-amine\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H16N2O3/c1-4-5-11(6-7(2)3)8(14)12-10(16)13-9(11)15/h4,7H,1,5-6H2,2-3H3,(H2,12,13,14,15,16)\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[[3,4-dioxo-2-[[(1r)-1-phenylpropyl]amino]-1-cyclobutenyl]amino]-2-hydroxy-n,n-dimethylbenzamide\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H16N4/c1-9(2)7-18-8-16-12-13(18)10-5-3-4-6-11(10)17-14(12)15/h3-6,8-9H,7H2,1-2H3,(H2,15,17)\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8ClN3O4S2/c8-4-1-5-7(2-6(4)16(9,12)13)17(14,15)11-3-10-5/h1-2,10-11H,3H2,(H2,9,12,13)\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H16F2N6OS/c1-8(6-25)21-14-13-15(22-11(19)5-20-13)24-16(23-14)26-7-9-3-2-4-10(17)12(9)18/h2-5,8,25H,6-7H2,1H3,(H3,19,21,22,23,24)/t8-/m1/s1\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][C][Branch2][Ring2][S][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@@H1][Branch1][=C][C][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][N][C][=Branch1][C][=O][C@@H1][Branch1][C][N][C][C][=C][N][=C][N][Ring1][Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C1CN2C[C@@H](N=C2S1)c3ccccc3\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H35ClN2O3/c25-22-4-3-20(30-8-2-6-26-5-1-7-28)12-21(22)23(29)27-16-24-13-17-9-18(14-24)11-19(10-17)15-24/h3-4,12,17-19,26,28H,1-2,5-11,13-16H2,(H,27,29)\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" N[C@H](Cc1c[nH]c2ccccc12)C(=O)O\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H16ClNO3S/c1-11-3-8-16-15(9-11)18(12(2)20(16)10-17(21)22)24(23)14-6-4-13(19)5-7-14/h3-9H,10H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-methoxy-3-(4-methoxyphenyl)-4-methylchromen-2-one\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H9NO4/c16-9-3-1-2-8(6-9)15-13(18)11-5-4-10(17)7-12(11)14(15)19/h1-7,16-17H\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" bag\\n\",\n        \"output\": \" bag is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)C(=O)c2cc(O)c(O)c(c2)[N+](=O)[O-]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(Nc1ccccn1)c2ccccc2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10O2/c16-15-13-9-5-4-8-12(13)10-14(17-15)11-6-2-1-3-7-11/h1-10H\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" recess\\n\",\n        \"output\": \" recess is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][Branch2][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25)\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H22N4O3/c1-25-16-6-3-13(4-7-16)12-27-17-8-5-14(10-18(17)26-2)9-15-11-23-20(22)24-19(15)21/h3-8,10-11H,9,12H2,1-2H3,(H4,21,22,23,24)\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCNC(=O)NS(=O)(=O)c1ccc(Cl)cc1\\n\",\n        \"output\": \" -0.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" crocodile\\n\",\n        \"output\": \" crocodile is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-ethylhexyl)-3-[[2-methoxy-4-[(2-methylphenyl)sulfonylcarbamoyl]phenyl]methyl]-1-methylindole-5-carboxamide\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-2-[(2,6-dichlorobenzoyl)amino]-3-[5-[3-(6-methylaminopyridin-2-yl)propyl]thiophen-2-yl]propanoic acid\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][P][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H19N3O4/c16-15(20)10-3-5-18(6-4-10)8-14(19)17-11-1-2-12-13(7-11)22-9-21-12/h1-2,7,10H,3-6,8-9H2,(H2,16,20)(H,17,19)\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-amino-8-(2,4-dimethoxypyrimidin-5-yl)-n-propylcinnoline-3-carboxamide\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1cc(F)cc(c1)c2cc(on2)N(CCCN3CCCCCC3)Cc4ccc5OCOc5c4\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1cc(nc2ccc(Nc3cc(nc(N)n3)c4cccc(Cl)c4)cc12)c5ccc(F)cc5\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][#Branch2][C][C][C][C][N][C][C][Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-furan-2-yl-1h-quinolin-4-one\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2][C][=Branch1][C][=O][C][=C][N][=C][Branch2][Ring1][Ring2][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][N][=C][Ring1][P][N]\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H8ClN3S/c10-7-3-1-6(2-4-7)5-8-12-13-9(11)14-8/h1-4H,5H2,(H2,11,13)\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][N][C][=Branch1][C][=O][N][C@H1][Branch1][N][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][N][Branch1][O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][#Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)N1CCC[C@H](CN2C(=O)c3cc(ccc3N=C2C(C)C)c4ccc(F)cc4)C1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[(6-chloroquinolin-4-yl)methyl]-5,7-bis(cyclopropylmethyl)-3-(3-methylimidazol-4-yl)pyrazolo[4,3-e]pyrimidine-4,6-dione\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch2][Ring1][Ring2][O][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H23FN6O3/c1-14(28)24-11-16-13-27(20(29)30-16)15-2-3-18(17(21)10-15)25-6-8-26(9-7-25)19-12-22-4-5-23-19/h2-5,10,12,16H,6-9,11,13H2,1H3,(H,24,28)/t16-/m0/s1\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H22FN7O3S/c1-28-7-9-29(10-8-28)33(31,32)18-5-4-14(11-16(18)22)17-13-25-20(23)19(27-17)21(30)26-15-3-2-6-24-12-15/h2-6,11-13H,7-10H2,1H3,(H2,23,25)(H,26,30)\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-amino-6-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-[4-(pyrrolidin-1-ylmethyl)pyridin-3-yl]pyrazine-2-carboxamide\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[(2-methyl-5-phenylfuran-3-carbonyl)amino]benzoic acid\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H10ClFN4/c15-11-6-9(2-3-12(11)16)20-14-10-5-8(17)1-4-13(10)18-7-19-14/h1-7H,17H2,(H,18,19,20)\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-n-[1-(2-methylsulfinylethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H29NO/c21-19(17-9-3-1-4-10-17,18-11-5-2-6-12-18)13-16-20-14-7-8-15-20/h1,3-4,9-10,18,21H,2,5-8,11-16H2\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][Branch2][Ring1][Ring2][C][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][C][C][Ring1][=Branch1][C][C][C][C][C][N][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)Cc3ccccc3C(=O)O)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ncnc2c1ncn2Cc3ccccc3\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ncc2CN=C(c3ccccc3F)c4cc(Cl)ccc4n12\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H12N2O/c1-7-6-10(13)12-9-5-3-2-4-8(9)11-7/h2-5,7,11H,6H2,1H3,(H,12,13)\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n'-(1h-indazol-4-yl)-n-(3-methylsulfonylphenyl)pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][Ring1][C][O][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16ClN3O/c18-12-5-6-15-13(11-12)17(21-9-7-19-8-10-21)20-14-3-1-2-4-16(14)22-15/h1-6,11,19H,7-10H2\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)c1ccc(C)c(NS(=O)(=O)c2ccc3N(C)SC(=O)c3c2)c1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H16ClNO2S/c1-11-3-8-16-15(9-11)18(12(2)20(16)10-17(21)22)23-14-6-4-13(19)5-7-14/h3-9H,10H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][=C][S][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H38O7S/c1-5-9-11-16(7-3)14-26-19(21)13-18(28(23,24)25)20(22)27-15-17(8-4)12-10-6-2/h16-18H,5-15H2,1-4H3,(H,23,24,25)\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H7N3/c9-8-6-3-1-2-4-7(6)10-5-11-8/h1-5H,(H2,9,10,11)\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1c2CCCCc2nc3ccccc13\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-6-(3,4-dichlorophenyl)-5,6-dihydro-3h-pyrimidin-4-one\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H15BrClNO4S/c1-23-15-7-4-12(18)10-14(15)19-16(20)8-9-24(21,22)13-5-2-11(17)3-6-13/h2-7,10H,8-9H2,1H3,(H,19,20)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" eyebrow\\n\",\n        \"output\": \" eyebrow is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16Cl2N2O3/c1-10-7-12(23-20-10)3-2-5-21-15-13(17)8-11(9-14(15)18)16-19-4-6-22-16/h7-9H,2-6H2,1H3\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCC(=CC1)c2cccc(O)c2\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H26N2OS2/c1-22-13-6-5-7-16(22)12-14-23-18-8-3-4-9-20(18)25-21-11-10-17(26(2)24)15-19(21)23/h3-4,8-11,15-16H,5-7,12-14H2,1-2H3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H18N6O3/c25-16(17-22-23-18(27-17)21-13-4-2-1-3-5-13)20-14-6-7-15(19-12-14)24-8-10-26-11-9-24/h1-7,12H,8-11H2,(H,20,25)(H,21,23)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" rotate\\n\",\n        \"output\": \" rotate is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-chlorophenyl)sulfonyl-4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidine-1-carboxamide\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H]1CN[C@@H](C2CC2)C(=O)N(C)[C@H](C)C(=O)N[C@H](Cc3ccc(F)cc3)C(=O)NCCCc4ccccc4O1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(COCc1ccccc1)Nc2ccc3c(c2)C(=O)C(=O)c4ccccc34\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CCO)CCCC(C)Nc1ccnc2cc(Cl)ccc12\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][C][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][O][=N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring2][Ring1][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cn1ncnc1COc2nn3c(nnc3cc2C(C)(C)C)c4cc(F)ccc4F\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" smoke\\n\",\n        \"output\": \" smoke is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H22ClFN4O4S/c1-30-18-11-17-14(10-19(18)31-13-6-8-27(9-7-13)32(2,28)29)21(25-12-24-17)26-16-5-3-4-15(22)20(16)23/h3-5,10-13H,6-9H2,1-2H3,(H,24,25,26)\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(Cc1oc2ccccc2c1C)C(=O)\\\\C=C\\\\c3cnc4NC(=O)CCc4c3\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COCCOC(=O)C1=C(C)NC(=C(C1c2cccc(c2)[N+](=O)[O-])C(=O)OC(C)C)C\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16ClNO4/c1-20-13-6-9(7-14(21-2)16(13)22-3)15(19)11-8-10(17)4-5-12(11)18/h4-8H,18H2,1-3H3\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][N][Branch2][Ring2][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 4.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15N3O2/c1-10(19)17-12-8-6-11(7-9-12)15(20)18-14-5-3-2-4-13(14)16/h2-9H,16H2,1H3,(H,17,19)(H,18,20)\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)c1ccc(NC(=O)c2cc(OC)c(OC)c(OC)c2)cc1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOc1ccc2nc(NC(=O)CC)sc2c1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)CCOc1ccc(N)cc1\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][=N][N][C][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccs2)N)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-chloro-n-hexyl-1-(phenylmethyl)quinolin-4-imine\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" [O-][N+](=O)c1ccc2c(c1)C(=O)C(=O)c3ccccc23\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11ClN2O2S/c1-8(16)15-9-3-2-4-10(5-9)17-7-11-6-14-12(13)18-11/h2-6H,7H2,1H3,(H,15,16)\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H17N5OS2/c1-9(7-21)17-12-11-13(18-14(16)23-11)20-15(19-12)22-8-10-5-3-2-4-6-10/h2-6,9,21H,7-8H2,1H3,(H3,16,17,18,19,20)/t9-/m1/s1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H15N3O3/c1-21-14-7-12-13(8-15(14)22-2)17-9-18-16(12)19-10-4-3-5-11(20)6-10/h3-9,20H,1-2H3,(H,17,18,19)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H20FN3O4/c1-11(21)18-9-13-10-20(16(22)24-13)12-2-3-15(14(17)8-12)19-4-6-23-7-5-19/h2-3,8,13H,4-7,9-10H2,1H3,(H,18,21)/t13-/m0/s1\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][Branch1][=N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][Ring2][Ring1][Ring1][=O]\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)Nc1nc(C)c(s1)c2cnc(F)c(NS(=O)(=O)c3sc(C)nc3C)c2\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=C]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" orchestra\\n\",\n        \"output\": \" orchestra is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H24ClNO4/c23-19-10-9-15(16-7-3-4-8-17(16)21(26)27)13-18(19)20(25)24-14-22(28)11-5-1-2-6-12-22/h3-4,7-10,13,28H,1-2,5-6,11-12,14H2,(H,24,25)(H,26,27)\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)\\\\C=C\\\\[C@H](C[C@@H]1CCNC1=O)NC(=O)[C@@H](CC(=O)[C@@H](NC(=O)c2cc(C)on2)C(C)C)Cc3ccc(F)cc3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-aminofluoren-9-one\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(4-methylpiperazin-1-yl)methyl]-n-[4-methyl-3-[(4-pyridin-3-ylpyrimidin-2-yl)amino]phenyl]benzamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][O][C][=Branch1][Branch2][=N][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H19N7S2/c1-2-6-16-15(5-1)19-18(27-16)24-9-7-23(8-10-24)13-17-20-21-22-25(17)12-14-4-3-11-26-14/h1-6,11H,7-10,12-13H2\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-furan-2-yl-1,5-di(phenyl)pyrazolo[4,5-e]pyrimidin-4-one\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H24ClN3S/c1-22-11-13-23(14-12-22)9-4-10-24-17-5-2-3-6-19(17)25-20-8-7-16(21)15-18(20)24/h2-3,5-8,15H,4,9-14H2,1H3\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H20FNO3/c20-15-3-1-13(2-4-15)17-7-8-21-10-14(17)11-22-16-5-6-18-19(9-16)24-12-23-18/h1-6,9,14,17,21H,7-8,10-12H2/t14-,17-/m0/s1\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][N][=C][Branch2][Ring1][=Branch1][C][=C][Ring1][Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch2][Ring1][#Branch1][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(CC(=O)Nc2nc3ccccc3[nH]2)cc1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H19N3O2S/c1-10-8-11(2)21-18-14(10)15(19)16(24-18)17(22)20-9-12-4-6-13(23-3)7-5-12/h4-8H,9,19H2,1-3H3,(H,20,22)\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)n2c(C)cc(C(=O)NS(=O)(=O)c3ccc(C)cc3)c2C\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H19NOS/c1-19-12-11-17(18-10-5-13-21-18)20-16-9-4-7-14-6-2-3-8-15(14)16/h2-10,13,17,19H,11-12H2,1H3/t17-/m0/s1\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-(phenylmethyl)indole-2-carboxylic acid\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=C][N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][F][N][=C][N][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C@@H1][C][C][C][N][Branch1][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[(2r)-2-amino-2-phenylethyl]-5-(1,3-benzodioxol-5-yl)-1-[(2,6-difluorophenyl)methyl]-6-methylpyrimidine-2,4-dione\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch2][Ring1][P]\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1cccc(NC(=O)c2ccccn2)c1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" methyl (2s)-2-(naphthalene-1-carbonylamino)-3-(4-nitrophenyl)propanoate\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)c2ccc3N=CN(C(=O)c3c2)c4cc(ccc4C)C(=O)Nc5ccon5\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H33N3O2/c1-15-20(9-19(27-15)13-25-4-2-23-3-5-25)21(26)24-14-22-10-16-6-17(11-22)8-18(7-16)12-22/h9,16-18,23H,2-8,10-14H2,1H3,(H,24,26)\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][C][C][C@@H1][Branch2][Ring1][#C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C3H5N3S/c1-2-5-6-3(4)7-2/h1H3,(H2,4,6)\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1cccc2C(=O)N(Cc3cccc(Cl)c3)C(=O)c12\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][NH1][C][=C][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H16ClNO2S/c1-11-7-8-15-13(9-11)18(12(2)20(15)10-17(21)22)23-16-6-4-3-5-14(16)19/h3-9H,10H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H11FN4O2/c16-13-4-2-1-3-12(13)9-20-18-14(17-19-20)10-5-7-11(8-6-10)15(21)22/h1-8H,9H2,(H,21,22)\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][C@@H1][Branch1][Branch2][N][=C][Ring1][Branch1][S][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-acetyl-3-[(4-fluorophenyl)methyl]-1-(phenylmethyl)pyrimidine-2,4-dione\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][N][=C][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][=Branch1][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][C][N][C][=Branch1][C][=O][N][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][N+1][=Branch1][C][=O][O-1][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfanyl-2-methyl-5-phenylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1cc2c(NC(NS2(=O)=O)C3CC4CC3C=C4)cc1Cl\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-chloro-5-(1-hydroxy-3-oxo-2h-isoindol-1-yl)benzenesulfonamide\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" frame\\n\",\n        \"output\": \" frame is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4,6-dichloro-3-[(e)-3-oxo-3-(phenylamino)prop-1-enyl]-1h-indole-2-carboxylic acid\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-ethyl-6-[[3-fluoro-5-(4-methoxyoxan-4-yl)phenoxy]methyl]quinolin-2-one\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(OC2CCN(CC2)C3CCN(CC3)C(=O)NS(=O)(=O)Cc4ccccc4)cc1Cl\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-amino-8-phenyl-n-propylcinnoline-3-carboxamide\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[(2r)-2-[[4-[[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]amino]quinazolin-5-yl]oxymethyl]pyrrolidin-1-yl]-2-hydroxyethanone\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][=N][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][C][Branch1][S][N][C][=C][C][=C][C][O][C][C][O][C][Ring1][#Branch2][=Ring1][=Branch1][=N][C][=N][C][Ring1][P][=C][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H22N2O3S/c1-14-5-9-18(10-6-14)23-16(3)13-20(17(23)4)21(24)22-27(25,26)19-11-7-15(2)8-12-19/h5-13H,1-4H3,(H,22,24)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][NH1][N][=C][C][=Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H](Cc1cccc(CC(=O)NC23CC4CC(CC(C4)C2)C3)c1)NC[C@H](O)c5ccc(O)c(CO)c5\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H30Cl2N4O/c25-22-9-8-21(15-23(22)26)27-24(31)30-13-11-28(12-14-30)17-20-7-4-10-29(18-20)16-19-5-2-1-3-6-19/h1-3,5-6,8-9,15,20H,4,7,10-14,16-18H2,(H,27,31)/t20-/m0/s1\\n\",\n        \"output\": \" 4.26\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[(2s)-1-hydroxypropan-2-yl]oxy-5-(4-methylsulfonylphenoxy)-n-(1,3-thiazol-2-yl)benzamide\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][#Branch1][N][C][=Branch1][C][=O][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring2][Ring1][=Branch1][N][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-piperidin-1-ylethyl 1h-indole-3-carboxylate\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1nc(CS(=O)(=O)c2ccccc2)cc(n1)N3CCOCC3\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-methyl-n'-(1,3-thiazol-2-yl)-1,2-oxazole-3,4-dicarboxamide\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)C(=O)c1ccc(cc1)C(N2CCNCC2)c3cccc4cccnc34\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-dimethylamino-n-[3-[[4-(2-methoxyethoxy)benzoyl]amino]-4-methylphenyl]benzamide\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C30H29N5O2/c1-20-29(36)33-28(22-7-3-2-4-8-22)27(31-20)23-13-11-21(12-14-23)19-34-17-15-24(16-18-34)35-26-10-6-5-9-25(26)32-30(35)37/h2-14,24H,15-19H2,1H3,(H,32,37)(H,33,36)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOC(=O)C(CCc1ccccc1)NC2CCc3ccccc3N(CC(=O)O)C2=O\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][Branch1][S][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][Br][NH1][Ring1][#C]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" icebreaker\\n\",\n        \"output\": \" icebreaker is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)S(=O)(=O)c1ccc(cc1)c2oc(SCC(=O)N3CCc4ccccc34)nn2\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-2-[4-(2-methylpropyl)phenyl]-n-methylsulfonylpropanamide\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H17FN2O3/c1-14(24)18-13-22(11-15-5-3-2-4-6-15)20(26)23(19(18)25)12-16-7-9-17(21)10-8-16/h2-10,13H,11-12H2,1H3\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1sc2ncnc(N3CCN(CC3)c4ncccn4)c2c1C\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C@@H1][Branch1][Ring2][C][Ring1][=Branch1][C][O][N][=C][Branch1][Ring2][N][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][#Branch2][N][C][=N][C][=C][Branch1][C][F][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=N][Ring1][=C][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-ethoxyphenyl)acetamide\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][=C][C][C][C][C][C][N][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H18FN3O/c1-2-18-5-7-19(8-6-18)15(20)14-10-11-9-12(16)3-4-13(11)17-14/h3-4,9-10,17H,2,5-8H2,1H3\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nnc(CCSCCc2nnc(N)s2)s1\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C1CC1Nc2ccc3nnc(c4ccccc4)n3n2\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H17Cl2N5/c1-3-22(4-2)15-14-16(20-9-19-15)23(10-21-14)8-11-12(17)6-5-7-13(11)18/h5-7,9-10H,3-4,8H2,1-2H3\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14O5/c1-7-9-3-5-11(15)8(2)13(9)19-14(18)10(7)4-6-12(16)17/h3,5,15H,4,6H2,1-2H3,(H,16,17)\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1C(=O)N(CCCCC(=O)C)C(=O)c2c1ncn2C\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H14O4S/c1-19-13-9-7-12(8-10-13)15(16)11-20(17,18)14-5-3-2-4-6-14/h2-10H,11H2,1H3\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccccc2)C(F)(F)F\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H11N3OS/c19-14(12-7-4-8-16-9-12)18-15-17-13(10-20-15)11-5-2-1-3-6-11/h1-10H,(H,17,18,19)\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][#Branch1][N][C][C][C][Ring1][Ring1][C][C][=C][Branch1][Branch1][O][N][=Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H11BrN2O/c16-12-7-5-11(6-8-12)15(19)9-18-10-17-13-3-1-2-4-14(13)18/h1-8,10H,9H2\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2ncc(F)c(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2n1\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][C][Branch1][C][F][=C][Ring1][Branch2][C][=Branch1][C][=O][N][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCSCCCNCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccnc2nc(nn12)C(=O)Nc3nccs3\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccccc1CNC(=O)c2ccccc2Oc3ccccc3\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5-chloro-1h-indol-2-yl)-(4-ethylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(2-fluoro-5-methylphenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][Branch1][C][N][S][C][C][C][C][C][C][Ring1][#Branch2][=Ring1][=Branch1]\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[[2-butyl-5-[(e)-3-hydroxy-3-oxo-2-(thiophen-2-ylmethyl)prop-1-enyl]imidazol-1-yl]methyl]benzoic acid\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H11BN2O2/c17-13-15-12-9-5-4-8-11(12)14(18)16(13)10-6-2-1-3-7-10/h1-9,18H,(H,15,17)\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H12Cl2N2O2S/c1-9-15(23-11-4-2-10(17)3-5-11)14-12(6-7-19-16(14)18)20(9)8-13(21)22/h2-7H,8H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)C1=C(C)NC(=C(C1c2ccccc2[N+](=O)[O-])C(=O)OC)C\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][N][=C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][Ring1][Branch2][=N][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" cushion\\n\",\n        \"output\": \" cushion is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][N][C][C][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H16N4S/c1-5(2)12(6(3)4)8-11-10-7(9)13-8/h5-6H,1-4H3,(H2,9,10)\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNS(=O)(=O)CCc1ccc2[nH]cc(C3CCN(C)CC3)c2c1\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nc(ns1)c2ccccc2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H22F3N3O4/c1-12(2)18(19(30)21(22,23)24)26-17(29)11-27-16(14-7-5-4-6-8-14)10-9-15(20(27)31)25-13(3)28/h4-10,12,18H,11H2,1-3H3,(H,25,28)(H,26,29)\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1cccc2c1c(c(C)n2CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-hydroxy-2-phenylisoindole-1,3-dione\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H20N2O3S/c26-22-21(16-17-29(28)20-14-8-3-9-15-20)23(27)25(19-12-6-2-7-13-19)24(22)18-10-4-1-5-11-18/h1-15,21H,16-17H2\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H9NOS/c15-10-6-7-11-12(8-10)16-13(14-11)9-4-2-1-3-5-9/h1-8,15H\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(C)nc(SCC(=O)N)n1\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cccc(OC)c1c2ccc(C[C@H](NC(=O)c3c(Cl)cccc3Cl)C(=O)O)cc2\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-phenylchromen-2-one\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H19N3O/c1-16-7-9-18(10-8-16)15(19)14-11-12-5-3-4-6-13(12)17(14)2/h3-6,11H,7-10H2,1-2H3\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 10-[3-(4-methylpiperazin-1-yl)propyl]-2-(trifluoromethyl)phenothiazine\\n\",\n        \"output\": \" 4.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4-bromophenyl) 1,4-diazabicyclo[3.2.2]nonane-4-carboxylate\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1C(=O)C2=C(OC(=CC2=O)O)c3ccccc13\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][#Branch2][C][C][C][C][C][=Branch1][C][=O][C][C][=Branch1][C][=O][C][=C][Ring1][#C][N][=C][N][Ring1][Branch1][C]\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n-dimethyl-1-phenothiazin-10-ylpropan-2-amine\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-[(2r)-3-dimethylamino-2-hydroxypropyl]benzamide\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H26N2O5/c1-21(2,10-13-4-6-15(27-3)7-5-13)22-11-18(25)16-8-14(24)9-17-20(16)28-12-19(26)23-17/h4-9,18,22,24-25H,10-12H2,1-3H3,(H,23,26)/t18-/m0/s1\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H29ClN4O6/c1-33-13-16(28)12-26-19(29)11-25-27(21(26)31)15-6-7-18(23)17(10-15)20(30)24-14-22(32)8-4-2-3-5-9-22/h6-7,10-11,16,28,32H,2-5,8-9,12-14H2,1H3,(H,24,30)/t16-/m0/s1\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H7NO4/c16-13-9-5-2-1-4-8(9)12-10(14(13)17)6-3-7-11(12)15(18)19/h1-7H\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxyisoquinoline\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(NC(=O)Nc2cccc(CNC(=O)O[C@H]3CCOC3)c2)ccc1c4ocnc4\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C28H38F3N5O2/c1-19-16-35(14-15-36(19)24(17-38-5)22-6-8-23(9-7-22)28(29,30)31)27(4)10-12-34(13-11-27)26(37)25-20(2)32-18-33-21(25)3/h6-9,18-19,24H,10-17H2,1-5H3/t19-,24-/m0/s1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-1,1-di(phenyl)ethanol\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1h-indol-2-yl-(4-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H13N5/c1-2-4-10(5-3-1)14-17-16-13-9-8-12(18-19(13)14)15-11-6-7-11/h1-5,8-9,11H,6-7H2,(H,15,18)\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H32O3/c1-12-9-15-17-6-5-16(13(2)23)22(17,4)11-19(25)20(15)21(3)8-7-14(24)10-18(12)21/h10,12,15-17,19-20,25H,5-9,11H2,1-4H3/t12-,15-,16+,17-,19-,20+,21-,22+/m0/s1\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)(C(=O)O)c1ccc(cc1)C(O)CCCN2CCC(CC2)C(O)(c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3,4-dichlorophenyl)-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carboxamide\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H27NO3/c1-2-14-22-15-18(23)16-25-21-11-7-6-10-19(21)20(24)13-12-17-8-4-3-5-9-17/h3-11,18,22-23H,2,12-16H2,1H3/t18-/m1/s1\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H14N4O4/c1-3-15(4-2-14(1)24-8-7-21-12-24)27-19-10-20(23-11-22-19)28-16-5-6-17-18(9-16)26-13-25-17/h1-12H,13H2\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCCOCCOCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H17F5N4O3/c1-8(2)14(15(29)18(21,22)23)26-13(28)7-27-16(25-6-12(24)17(27)30)9-3-10(19)5-11(20)4-9/h3-6,8,14H,7,24H2,1-2H3,(H,26,28)\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(4-methoxypyridin-2-yl)methylsulfanyl]-1h-benzimidazole\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1C(=O)C=Cc2cc(COc3cc(F)cc(c3)C4(CCOCC4)OC)ccc12\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Nc1ccccc1)c2oc3ccccc3c2\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-methyl-2-morpholin-4-yl-9-[1-(phenylamino)ethyl]pyrido[2,1-b]pyrimidin-4-one\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[[(5s)-3-[4-(1,3-dihydropyrrolo[3,4-c]pyridin-2-yl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H26ClN3O2/c21-16-8-9-17-15(7-10-18(23-17)22-11-4-12-25)20(16)24-19(26)13-14-5-2-1-3-6-14/h7-10,14,25H,1-6,11-13H2,(H,22,23)(H,24,26)\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H26ClNO/c1-21(17-7-4-3-5-8-17,18-10-12-19(22)13-11-18)24-16-14-20-9-6-15-23(20)2/h3-5,7-8,10-13,20H,6,9,14-16H2,1-2H3\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][O][C][Branch2][Ring1][Ring2][S][C][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][=N][N][=Ring2][Ring1][C]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3-dimethylaminopropyl)-4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]-n-methylbenzenesulfonamide\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][C@@H1][C][N][Branch1][#Branch2][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][C][N][Ring1][=N][C][C@@H1][Branch1][C][O][C][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@@H1][C@H1][Branch1][C][O][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][O][C][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][Branch2][Ring2][P][C][O][C][=C][C][Branch1][#Branch2][O][C][C][C][O][C][C][Ring1][=Branch1][=C][C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=N][C][=N][C][Ring1][P][=C][Ring2][Ring1][N][C][C][Ring2][Ring2][Ring2]\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H27ClN2O/c1-17(2)24-14-12-21(13-15-24)25(20-10-8-19(23)9-11-20)22(26)16-18-6-4-3-5-7-18/h3-11,17,21H,12-16H2,1-2H3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" vacuum\\n\",\n        \"output\": \" vacuum is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" benzo[b][1]benzazepine-11-carboxamide\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1,3-thiazol-2-yl)pyridine-3-carboxamide\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][C][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-naphthalen-1-yl-n-phenylacetamide\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCCC(CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H30N2O5S/c29-22-10-9-21(25-24(22)28-26(31)34-25)23(30)17-27-12-4-13-32-15-16-33-14-11-19-7-3-6-18-5-1-2-8-20(18)19/h1-3,5-10,23,27,29-30H,4,11-17H2,(H,28,31)/t23-/m0/s1\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)Oc1ccc2C(=O)C(=COc2c1)c3ccccc3\\n\",\n        \"output\": \" 4.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 2-[(4-chlorophenyl)sulfonyl-(2-methylphenyl)amino]acetate\\n\",\n        \"output\": \" 4.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2-phenylphenyl)benzenesulfonamide\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][=C][S][C][=Branch1][Ring2][=N][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-chloro-n-[2-(2-chlorophenyl)ethyl]-5-(3,5-dioxo-1,2,4-triazin-2-yl)benzamide\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-[(2-chloro-6-fluorophenyl)amino]-5-methylphenyl]acetic acid\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1,2-bis(4-fluorophenyl)-2-hydroxyethanone\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-methoxy-n-pyridin-2-ylbenzenesulfonamide\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-amino-2-(2-methoxyethoxy)-9-(phenylmethyl)-7h-purin-8-one\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H24N4O6/c1-30-20-10-17(5-6-19(20)21-12-24-14-32-21)27-22(28)26-16-4-2-3-15(9-16)11-25-23(29)33-18-7-8-31-13-18/h2-6,9-10,12,14,18H,7-8,11,13H2,1H3,(H,25,29)(H2,26,27,28)/t18-/m0/s1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H20N4O3S/c1-26(23,24)12-15-11-17(22-6-8-25-9-7-22)21-18(20-15)14-2-3-16-13(10-14)4-5-19-16/h2-5,10-11,19H,6-9,12H2,1H3\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-methyl-1-(4-methylphenyl)-3-piperidin-1-ylpropan-1-one\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H12O3/c1-7-4-12(15)17-14-9(3)13-10(6-11(7)14)5-8(2)16-13/h4-6H,1-3H3\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H8Br2O4/c15-7-1-3-11(17)9(5-7)13(19)14(20)10-6-8(16)2-4-12(10)18/h1-6,17-18H\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C][Branch1][Ring2][C][C][=C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][O][=O]\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-nitro-4-quinolin-8-yloxybenzamide\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=N][C][Branch1][C][N][=C][Branch1][Ring2][S][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H9N3O2S2/c15-18(16,11-5-2-6-17-11)14-10-4-1-3-9-8(10)7-12-13-9/h1-7,14H,(H,12,13)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Brc1ccccc1C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 4.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3Cc4ccncc4C3)c(F)c2\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][Branch1][O][N][C][C][=C][C][=C][N][=C][Ring1][=Branch1][=N][N][Ring1][P][Ring1][=C]\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H36N2O4/c1-4-33-25-17-20(12-13-22(25)27(31)32)18-26(30)28-23(16-19(2)3)21-10-6-7-11-24(21)29-14-8-5-9-15-29/h6-7,10-13,17,19,23H,4-5,8-9,14-16,18H2,1-3H3,(H,28,30)(H,31,32)/t23-/m0/s1\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" eyelash\\n\",\n        \"output\": \" eyelash is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[(4-chlorophenyl)sulfonylmethyl]-2-methyl-6-morpholin-4-ylpyrimidine\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H28N4O6S/c1-37-26-15-19(27(33)31-39(35,36)24-9-3-2-4-10-24)11-12-21(26)18-32-25-16-22(14-13-20(25)17-29-32)30-28(34)38-23-7-5-6-8-23/h2-4,9-17,23H,5-8,18H2,1H3,(H,30,34)(H,31,33)\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCCN4CCCCC4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H21N5O/c1-15(26-16(2)29)17-3-6-21(7-4-17)27-23-25-14-20-13-19(5-8-22(20)28-23)18-9-11-24-12-10-18/h3-15H,1-2H3,(H,26,29)(H,25,27,28)/t15-/m1/s1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nnc(c(N)n1)c2cccc(Cl)c2Cl\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)c1c(C)n(Cc2occc2)c3ccc(O)cc13\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NS(=O)(=O)c1cc2c(NC(Cc3ccccc3)NS2(=O)=O)cc1C(F)(F)F\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-[3-(3-hydroxypropylamino)propoxy]benzamide\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H19Cl2NO2/c15-8-10-17(11-9-16)13-6-4-12(5-7-13)2-1-3-14(18)19/h4-7H,1-3,8-11H2,(H,18,19)\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCN(CCC)S(=O)(=O)c1ccc(cc1)C(=O)O\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s,5s)-5-(hydroxymethyl)-1-methyl-2-propan-2-yl-2,4,5,6-tetrahydro-1,4-benzodiazocin-3-one\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCc1c(O)c(ccc1OCCCSc2ccc(CC(=O)O)cc2Cl)C(=O)CC\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][=C][C][=C][C][=C][N][Ring1][=Branch1][C][=Ring1][=Branch2][C][=C][C][=N][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=N][Ring1][=C]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H16N4O2S/c1-20(2)14-7-3-6-13-12(14)5-4-8-15(13)23(21,22)19-16-11-17-9-10-18-16/h3-11H,1-2H3,(H,18,19)\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][S][C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][=C][N][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (3,3,5-trimethylcyclohexyl) 2-hydroxy-2-phenylacetate\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)-7-methoxy-6-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H13NO4/c21-15-10-16(22)24-18-13-8-4-5-9-14(13)20(19(23)17(15)18)11-12-6-2-1-3-7-12/h1-10,22H,11H2\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H29N5O5S/c1-13(2)30-21(27)26-10-8-16(9-11-26)31-20-14(3)19(22-12-23-20)25-17-6-7-18(24-15(17)4)32(5,28)29/h6-7,12-13,16H,8-11H2,1-5H3,(H,22,23,25)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[2-oxo-2-[[3-(trifluoromethyl)phenyl]amino]ethyl]-1h-indole-2-carboxylic acid\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][=C][Branch1][C][N][S][C][Ring2][Ring1][C][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][N][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][B][Ring1][#Branch2][O]\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][Branch2][Ring1][=N][C][C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" -0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-bromoquinazoline-2,4-diamine\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][C][N][Branch1][=Branch2][C][C@H1][Branch1][C][C][N][Ring1][#Branch1][C][=C][Branch1][C][F][C][Branch1][C][N][=C][C][=Branch1][C][=O][C][=Branch1][P][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring1][#Branch2][=C][Ring1][S][F][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" cyclohexanecarboxamide\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][NH1][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch2][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (5-methoxy-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" girl\\n\",\n        \"output\": \" girl is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][#C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C29H33ClN2O2/c1-31(2)27(33)29(24-9-5-3-6-10-24,25-11-7-4-8-12-25)19-22-32-20-17-28(34,18-21-32)23-13-15-26(30)16-14-23/h3-16,34H,17-22H2,1-2H3\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H26N2O4/c1-28-21-10-4-5-11-22(21)29-14-13-25-15-17(27)16-30-23-12-6-9-20-24(23)18-7-2-3-8-19(18)26-20/h2-12,17,25-27H,13-16H2,1H3\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H29N5O7/c1-2-37-26-18(14-21(33)38-26)29-23(34)19-8-5-13-30-20(32)10-9-17(25(36)31(19)30)28-24(35)22-16-7-4-3-6-15(16)11-12-27-22/h3-4,6-7,11-12,17-19,26H,2,5,8-10,13-14H2,1H3,(H,28,35)(H,29,34)/t17-,18-,19-,26+/m0/s1\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" seaplane\\n\",\n        \"output\": \" seaplane is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch2][Ring1][O][C][N][C][=N][NH1][C][=C][C][=N][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][S][Ring1][=N][=C][Ring2][Ring1][#Branch2]\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H13ClN6O2S2/c1-8(24)25-6-5-23-14-11(13(18)19-7-20-14)22-15(23)27-16-21-10-4-2-3-9(17)12(10)26-16/h2-4,7H,5-6H2,1H3,(H2,18,19,20)\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][N][C][=Branch1][C][=O][C][Branch2][Ring1][P][N][Branch1][=Branch2][C][C][O][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Ring2][NH1][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCn1c2ccccc2c3cc(NC(=O)CCc4ccncc4)ccc13\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Branch1][#C][N][C][=C][C][=C][C][C][C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(C(=O)C)c1cccc2c1c(Sc3ccc(Cl)cc3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3-yl]-n-(1,2-oxazol-3-yl)benzamide\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H13N3O4S2/c1-8-7-15-14(22-8)16-13(19)11-12(18)9-5-3-4-6-10(9)23(20,21)17(11)2/h3-7,11H,1-2H3,(H,15,16,19)\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H20F4N4O5/c1-10(2)15(16(30)20(22,23)24)27-14(29)9-28-17(11-4-6-12(21)7-5-11)25-8-13(18(28)31)26-19(32)33-3/h4-8,10,15H,9H2,1-3H3,(H,26,32)(H,27,29)\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H26Cl2FN3O4S/c24-21-6-3-19(15-22(21)25)33-18-9-13-28(14-10-18)17-7-11-29(12-8-17)23(30)27-34(31,32)20-4-1-16(26)2-5-20/h1-6,15,17-18H,7-14H2,(H,27,30)\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H16N2O2/c21-18(22)15-10-13-12-8-4-5-9-14(12)19-17(13)16(20-15)11-6-2-1-3-7-11/h1-9,15-16,19-20H,10H2,(H,21,22)\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[3-chloro-4-(4-chlorophenoxy)phenyl]-6,6-dimethyl-1,3,5-triazine-2,4-diamine\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)N1CCC[C@H](CN2C(=Nc3ccc(Oc4ccc(F)cc4)cc3C2=O)C)C1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-thiophen-2-yl-1,3-thiazol-2-yl)acetamide\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=C(C(=O)c2ccc(O)cc2O1)c3ccccc3\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(2,5-dimethylphenoxy)-2,2-dimethylpentanoic acid\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H21NO2/c1-3-18-14(17)15(9-11-16(2)12-10-15)13-7-5-4-6-8-13/h4-8H,3,9-12H2,1-2H3\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][Branch2][Ring1][=C][O][C][=C][C][=Branch1][#Branch1][=C][N][=C][Ring1][=Branch1][N][C][C][=N][N][Branch1][Ring2][C][=Ring1][Branch1][C][C][C][N][C][C][Ring1][=Branch1][C][=C][Branch1][C][Cl][C][=C][C][Branch1][C][F][=C][Ring1][Branch2][Cl]\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OC\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][C][C][Ring1][=Branch1][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2]\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H11ClN2O5S/c13-9-5-10(15-6-7-2-1-3-20-7)8(12(16)17)4-11(9)21(14,18)19/h1-5,15H,6H2,(H,16,17)(H2,14,18,19)\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H12O3/c1-10-13(12(14)7-8-15-10)16-9-11-5-3-2-4-6-11/h2-8H,9H2,1H3\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC[C@H]1[C@@H](Cc2cncn2C)COC1=O\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][S][N][C][=Branch1][C][=O][C][C][C][=C][C][=N][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Branch2][Ring1][P]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H18N4OS/c1-21(2)12-8-9-19-17-13(12)14(18)15(23-17)16(22)20-10-11-6-4-3-5-7-11/h3-9H,10,18H2,1-2H3,(H,20,22)\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" hygienic\\n\",\n        \"output\": \" hygienic is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl-di(propan-2-yl)-[2-(9h-xanthene-9-carbonyloxy)ethyl]azanium\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][N][=C][N][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(1r)-1'-(9h-carbazol-3-ylmethyl)spiro[1,2-dihydroindene-3,4'-piperidine]-1-yl]acetamide\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H15ClN4/c21-15-5-7-16(8-6-15)23-20-18-4-2-1-3-17(18)19(24-25-20)13-14-9-11-22-12-10-14/h1-12H,13H2,(H,23,25)\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[6-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-amino-6-(4-morpholin-4-ylsulfonylphenyl)-n-pyridin-3-ylpyrazine-2-carboxamide\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch2][Ring1][P][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H26BrN5O4/c24-15-1-3-19-18(11-15)29(22(31)14-33-19)10-9-28-7-5-16(6-8-28)25-12-17-2-4-20-23(26-17)27-21(30)13-32-20/h1-4,11,16,25H,5-10,12-14H2,(H,26,27,30)\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c(CN(C)C)c(nc2ccccc12)c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 4.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" quinoline\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1cnc(NC(=O)[C@H](CC2CCOCC2)c3ccc(cc3)S(=O)(=O)C4CC4)s1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][S][N][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][=Branch1][Cl][=C][Ring1][P]\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H19Cl2N3O6S3/c22-14-1-6-18(25-34(28,29)20-8-7-19(23)33-20)17(13-14)21(27)24-15-2-4-16(5-3-15)35(30,31)26-9-11-32-12-10-26/h1-8,13,25H,9-12H2,(H,24,27)\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][C][=C][N][Branch1][=C][C][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][S][C][=Branch2][Ring1][#Branch2][=C][Branch1][#C][C][N][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][#C][C][Ring2][Ring1][N][=O][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][C][C][C][=C][Ring1][N]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-2-amino-3-(1h-indol-3-yl)propanoic acid\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][O][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H29ClN4O/c22-18-12-24-19(26-3-1-23-2-4-26)8-17(18)20(27)25-13-21-9-14-5-15(10-21)7-16(6-14)11-21/h8,12,14-16,23H,1-7,9-11,13H2,(H,25,27)\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CS(=O)(=O)c1cccc(Nc2nccc(Nc3cccc4[nH]ncc34)n2)c1\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H18ClFN2/c20-14-1-6-19-17(11-14)18(13-7-9-22-10-8-13)12-23(19)16-4-2-15(21)3-5-16/h1-6,11-13,22H,7-10H2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)c1ccnc2sc(C(=O)NCc3ccccc3)c(N)c12\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)C(=O)N2CCC(CC2)C(=O)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H14ClN3O/c1-12-11-16(21(20-12)15-5-3-2-4-6-15)19-17(22)13-7-9-14(18)10-8-13/h2-11H,1H3,(H,19,22)\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15ClN2OS/c1-20-15-13(3-2-9-18-15)14(19)17-10-8-11-4-6-12(16)7-5-11/h2-7,9H,8,10H2,1H3,(H,17,19)\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][C][=N][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOc1ccc(cc1)c2cnc3CCCCCn23\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O-1][C][=C][C][=Branch1][S][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N+1][Ring2][Ring1][Ring1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][Branch2][Ring2][Ring2][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1oc(CN2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][N][=C][Branch1][#C][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][#C]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][S][C][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-[[2-(2,5-dioxopyrrolidin-1-yl)acetyl]amino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-pyridin-3-ylthiophene-2-sulfonamide\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-(4-ethylsulfanylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][N][=C][Branch1][Ring1][O][C][N][=C][Ring1][Branch2][O][C]\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(4-imidazo[2,3-f]pyridazin-3-ylpyrimidin-2-yl)amino]-n-methylbenzenesulfonamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-[[[1-[2-(6-bromo-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2nc(nc(N)c2cc1OC)N3CCN(CC3)C(=O)C4CCCO4\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][=Branch1][=C][C][Ring1][#Branch1][=O][C][Branch2][Ring1][#Branch2][C][C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][Ring2][Ring1][N][N][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)-6-(3-dimethylaminopropoxy)-7-methoxyquinazolin-4-amine\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H14F3N3O2S/c1-11-2-4-12(5-3-11)15-10-16(17(18,19)20)22-23(15)13-6-8-14(9-7-13)26(21,24)25/h2-10H,1H3,(H2,21,24,25)\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C4H6N4O3S2/c1-2(9)6-3-7-8-4(12-3)13(5,10)11/h1H3,(H2,5,10,11)(H,6,7,9)\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H32FN7O4/c1-3-35(9-10-36)8-5-11-39-24-16-22-21(15-23(24)38-2)27(30-17-29-22)32-25-13-20(33-34-25)14-26(37)31-19-7-4-6-18(28)12-19/h4,6-7,12-13,15-17,36H,3,5,8-11,14H2,1-2H3,(H,31,37)(H2,29,30,32,33,34)\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H25ClFN5O2/c1-33-22-14-20-17(24(28-15-27-20)29-16-7-8-19(26)18(25)12-16)13-21(22)30-23(32)6-5-11-31-9-3-2-4-10-31/h5-8,12-15H,2-4,9-11H2,1H3,(H,30,32)(H,27,28,29)/b6-5+\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][N][=C][Branch1][Ring1][C][O][C][=Ring1][#Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1cccc(c1)N2C(=O)c3ccc(O)cc3C2=O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-propan-2-ylpyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H12N2S/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10/h1-5,10H,6-8H2/t10-/m1/s1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-(4-methylpiperazin-1-yl)phenyl]quinolin-4-amine\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-morpholin-4-yl-2-(phenoxy)ethanone\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@H]([C@H](Cc1ccccc1)NC(=O)c2cc3cc(Cl)ccc3[nH]2)C(=O)N4C[C@@H](O)[C@@H](O)C4\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H31BrN8O3/c1-23(2,19(25)33)20(34)27-10-6-9-26-18-17(24)14-28-21(31-18)29-15-7-5-8-16(13-15)30-22(35)32-11-3-4-12-32/h5,7-8,13-14H,3-4,6,9-12H2,1-2H3,(H2,25,33)(H,27,34)(H,30,35)(H2,26,28,29,31)\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H32N2O5/c1-3-30-23(29)18(13-12-16-8-5-4-6-9-16)24-15(2)21(26)25-19-11-7-10-17(19)14-20(25)22(27)28/h4-6,8-9,15,17-20,24H,3,7,10-14H2,1-2H3,(H,27,28)/t15-,17-,18-,19-,20-/m0/s1\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[[3-(trifluoromethyl)phenyl]amino]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN(C)[C@H](C)C(=O)N\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[[(5s)-3-(3-fluoro-4-morpholin-4-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-[[4-methyl-6-(1-methylbenzimidazol-2-yl)-2-propylbenzimidazol-1-yl]methyl]phenyl]benzoic acid\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2-amino-3h-benzimidazol-5-yl)-phenylmethanone\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H23N3O/c1-21(2)13-8-14-23-19-17-11-6-7-12-18(17)22(20-19)15-16-9-4-3-5-10-16/h3-7,9-12H,8,13-15H2,1-2H3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H19N3S/c1-2-22-21-20(18-13-8-14-25-18)24-19(15-9-4-3-5-10-15)16-11-6-7-12-17(16)23-21/h3-14,20H,2H2,1H3,(H,22,23)\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=C][C][C][C][N][Ring1][Branch1][C][=Ring1][Branch2][Br]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-(2-chlorophenyl)-7-nitro-1,3-dihydro-1,4-benzodiazepin-2-one\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-ethylsulfinyl-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [4-amino-2-[(1-methylsulfonylpiperidin-4-yl)amino]pyrimidin-5-yl]-(2,3-difluoro-6-methoxyphenyl)methanone\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H8N2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H,(H2,10,11)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch2][Ring1][=Branch1][N][C][C][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)S(=O)(=O)c2ccc(c(C)c2)c3cnc(N)c(n3)C(=O)Nc4cccnc4\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][Branch1][N][C][C][=C][C][Branch1][C][F][=C][C][=Ring1][#Branch1][=C][Branch1][Ring2][NH1][Ring1][N][C][C][=C][N][=C][C][=Ring1][=Branch1]\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(NC(=O)C=C)cc1\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H13NO2/c15-14(16)12-8-4-5-9-13(12)17-10-11-6-2-1-3-7-11/h1-9H,10H2,(H2,15,16)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(ccc1Nc2ccccc2C(=O)O)c3ccc(Nc4ccccc4C(=O)O)c(OC)c3\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][P][\\\\C][=C][\\\\C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][/-Ring1][#Branch2][=O][C][=C][Ring2][Ring1][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(C1CCN(CC1)c2nnc(s2)n3cccc3)N4CCN(Cc5ccc6OCOc6c5)CC4\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(hydroxymethyl)-5-methyl-n-(1,3-thiazol-2-yl)-1,2-oxazole-4-carboxamide\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CCCOc1nccc(Nc2cc(NC(=O)c3ccnc(c3)N4CCOCC4)ccc2C)n1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=N][N][C][C][C][C][Ring1][Branch1][=C][Ring1][Branch2][C][=C][C][=N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" c1ccc2ccccc2c1\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[5-(3-cyclohexylpropanoylamino)-2-methylphenyl]-4-hydroxybenzamide\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4-ethylpiperazin-1-yl)-(5-fluoro-1h-indol-2-yl)methanone\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[[(5s)-3-[4-(5,7-dihydropyrrolo[3,4-b]pyridin-6-yl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H19NO4/c1-22-15-6-4-13(5-7-15)17(20)14-8-10-19(11-9-14)18(21)16-3-2-12-23-16/h2-7,12,14H,8-11H2,1H3\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][Branch1][S][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC[C@@H](NC1=C(Nc2cccc(C(=O)N(C)C)c2O)C(=O)C1=O)c3oc(C)cc3\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H24N2O3/c1-13(2)7-5-9(6-8-13)15-12(18)10(14)3-4-11(16)17/h9-10H,3-8,14H2,1-2H3,(H,15,18)(H,16,17)/t10-/m0/s1\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][#Branch2][S][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][Ring1][P][C]\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][N][=C][N][C][=Ring1][Branch1][C][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H12N4O3S/c1-18-11-10(13-6-7-14-11)15-19(16,17)9-4-2-8(12)3-5-9/h2-7H,12H2,1H3,(H,13,15)\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(benzoyl)-2,3-dihydro-1h-pyrrolizine-1-carboxylic acid\\n\",\n        \"output\": \" -0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H11ClN2O4S/c15-11-6-5-8(7-12(11)22(16,20)21)14(19)10-4-2-1-3-9(10)13(18)17-14/h1-7,19H,(H,17,18)(H2,16,20,21)\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H20N4O3S/c25-28(26,17-6-2-1-3-7-17)15-16-14-19(24-10-12-27-13-11-24)23-20(22-16)18-8-4-5-9-21-18/h1-9,14H,10-13,15H2\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-2-[4-(2-methylpropyl)phenyl]-n-methylsulfonylpropanamide\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-amino-5-(4-chlorophenyl)thiophene-2-carboxamide\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-[[1-(2-hydroxyethyl)-3-methyl-5-phenylpyrazol-4-yl]methyl]-n-(3-methoxyphenyl)benzamide\\n\",\n        \"output\": \" 4.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H38O6/c1-5-15(3)24(29)30-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-18(25)12-19(26)13-22(27)28/h6-7,10,14-16,18-21,23,25-26H,5,8-9,11-13H2,1-4H3,(H,27,28)/t14-,15-,16-,18+,19+,20-,21-,23-/m0/s1\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H24ClN5O2/c23-15-6-7-20-18(14-15)25-22(30)28(20)16-8-12-26(13-9-16)10-3-11-27-19-5-2-1-4-17(19)24-21(27)29/h1-2,4-7,14,16H,3,8-13H2,(H,24,29)(H,25,30)\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H17NO/c18-16(14-7-2-1-3-8-14)12-17-11-10-13-6-4-5-9-15(13)16/h1-9,17-18H,10-12H2\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-fluorophenyl)-4-[[(3s)-piperidin-3-yl]amino]thieno[2,3-d]pyridine-7-carboxamide\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C(CN1CCCCC1)C2CCc3cc(OCc4ccc(cc4)c5ccccc5)ccc3C2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H24ClN3O/c1-25-13-4-5-18(12-14-25)26-22(27)20-7-3-2-6-19(20)21(24-26)15-16-8-10-17(23)11-9-16/h2-3,6-11,18H,4-5,12-15H2,1H3\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H9NOSe/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(2-methoxyphenyl)methyl]-1,6-naphthyridine-2-carboxamide\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H12Cl2N2O/c1-7(11-14-5-6-15-11)16-10-8(12)3-2-4-9(10)13/h2-4,7H,5-6H2,1H3,(H,14,15)\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][O][C][=C][C][=C][Branch1][O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][Ring2][=C][Ring1][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C@H1][C][C][C@@H1][Branch1][#C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring2][Ring1][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H14O3/c1-11(15(16)17)12-6-5-9-14(10-12)18-13-7-3-2-4-8-13/h2-11H,1H3,(H,16,17)\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H27ClN2O3/c1-17-15-25(11-12-26(17)22(27)13-18-5-3-2-4-6-18)16-20-14-21(24)9-7-19(20)8-10-23(28)29/h2-7,9,14,17H,8,10-13,15-16H2,1H3,(H,28,29)/t17-/m0/s1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=C][C][=C][C][Branch2][Ring2][#Branch2][C][C][C][C][=C][C][=C][Branch2][Ring1][N][C][C@H1][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=Branch1][C][=O][O][S][Ring2][Ring1][Branch1][=N][Ring2][Ring1][=C]\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s,3s)-n'-hydroxy-1-methyl-n-[4-[(2-methylquinolin-4-yl)methoxy]phenyl]piperidine-2,3-dicarboxamide\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1ccc2c3ccccc3C(=O)c2c1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C][N][Branch2][Ring1][Ring1][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch2][Ring2][#Branch2][C][C][=C][C][=C][C][Branch2][Ring1][=N][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][=C][Ring2][Ring1][Branch2][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Ring1][N]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H8Cl2N2S/c9-6-2-1-5(3-7(6)10)4-13-8(11)12/h1-3H,4H2,(H3,11,12)\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][N][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-2-[[2-(3,5-difluorophenyl)acetyl]amino]-n-(5-methyl-6-oxo-7h-benzo[d][1]benzazepin-7-yl)propanamide\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-methyl-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-thiophen-2-yl-7-(trifluoromethyl)-[1,2,4]triazolo[1,5-a]pyrimidin-2-amine\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-dimethylamino-3-[4-[[5-methyl-4-(phenylamino)pyrimidin-2-yl]amino]phenoxy]propan-2-ol\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-chloro-2-[[(3s)-4-[2-(4-chlorophenyl)acetyl]-3-methylpiperazin-1-yl]methyl]phenyl]acetic acid\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H13NO2/c18-16(19)15-10-13-8-4-5-9-14(13)17(15)11-12-6-2-1-3-7-12/h1-10H,11H2,(H,18,19)\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14-,19+,20-/m0/s1\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O[C@@H](CNCCc1ccc(NC[C@H](O)c2ccccc2)cc1)c3ccc(O)c(NC=O)c3\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(carbamoylamino)-5-(3,5-difluorophenyl)-n-[(3s)-piperidin-3-yl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-methyl-n-[4-nitro-3-(trifluoromethyl)phenyl]propanamide\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]-n-(4-methylphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Br][=C][C][Branch1][Ring1][O][C][=C][Ring1][=Branch2][O][C]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (e,3r,5s)-7-[4-(4-fluorophenyl)-5-(methoxymethyl)-2,6-di(propan-2-yl)pyridin-3-yl]-3,5-dihydroxyhept-6-enoic acid\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-1-morpholin-4-yl-2-[4-[[1-(pyridin-2-ylmethyl)indazol-5-yl]amino]quinazolin-5-yl]oxypropan-1-one\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H14Cl2F2N2O3/c18-11-6-22-7-12(19)15(11)23-16(24)10-3-4-13(26-17(20)21)14(5-10)25-8-9-1-2-9/h3-7,9,17H,1-2,8H2,(H,22,23,24)\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H11Cl2NO2/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19/h1-7,17H,8H2,(H,18,19)\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][=C][C][C][C][N][Branch2][Ring2][C][C][C][C][Branch2][Ring1][Ring2][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring1][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][N][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-[(1r)-2-[3-[2-[2-(2-chlorophenyl)ethylamino]ethylsulfanyl]propylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" FC(F)c1nc2ccccc2n1c3nc(nc(n3)N4CCOCC4)N5CCOCC5\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H25Cl2N3O4/c25-21-6-5-17(11-22(21)26)33-16-7-9-29(10-8-16)14-15(30)12-27-24(32)20-13-28-23(31)19-4-2-1-3-18(19)20/h1-6,11,13,15-16,30H,7-10,12,14H2,(H,27,32)(H,28,31)/t15-/m1/s1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H6O3/c8-6-4-2-1-3-5(6)7(9)10/h1-4,8H,(H,9,10)\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)\\\\C(=N/OCOCCOC)\\\\[C@H](C)[C@@H](O)[C@]1(C)O\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)NC1CC2CCCC(C1)N2C(=O)Nc3ccc(Cl)c(c3)C(F)(F)F\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(C)NC[C@H](O)COc1nsnc1N2CCOCC2\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H26N6O/c1-4-15(11-26)22-19-23-17(20-10-14-8-6-5-7-9-14)16-18(24-19)25(12-21-16)13(2)3/h5-9,12-13,15,26H,4,10-11H2,1-3H3,(H2,20,22,23,24)/t15-/m1/s1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H26N2O2/c1-5-7-15-12-16(19-14(4)20)8-9-17(15)21-11-6-10-18-13(2)3/h5,8-9,12-13,18H,1,6-7,10-11H2,2-4H3,(H,19,20)\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][Branch1][P][C][=N][N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][=Branch2][O][C][C@@H1][Branch1][C][O][C][O][=C][Ring1][N]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)quinazoline-4,6-diamine\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][C][C][O][C][=C][C][=N][C][Branch2][Ring1][Ring1][C][S+1][Branch1][C][O-1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-propan-2-ylphenyl)-5-(thiophen-2-ylmethylsulfanyl)-2h-1,2,4-triazol-3-amine\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][O][N][C][N][S][Ring1][=Branch1][=Branch1][C][=O][=O][C][=C][Ring1][N][Cl]\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1C(=O)N(Cc2ccc(Br)cc2)c3ccccc13\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C32H45N3O4S/c1-4-35(32(37)24-26-10-12-30(13-11-26)40(3,38)39)29-16-19-33(20-17-29)21-18-31(28-8-6-5-7-9-28)34-22-14-27(15-23-34)25(2)36/h5-13,27,29,31H,4,14-24H2,1-3H3\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-pyridin-4-yl-3,4-dihydro-1h-isoquinoline\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H14FN3O3/c20-14-6-5-11(10-16(14)23-17(24)7-8-18(23)25)9-15-12-3-1-2-4-13(12)19(26)22-21-15/h1-6,10H,7-9H2,(H,22,26)\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring1][#C][N][C][=Branch1][C][=S][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H14ClN3O5/c1-29-20(28)11-4-2-3-10(7-11)9-24-19(27)15-16(18(26)23-24)22-14-8-12(21)5-6-13(14)17(15)25/h2-8H,9H2,1H3,(H,22,25)(H,23,26)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][F][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][Branch1][C][C][C][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-yl]-n-(4-propan-2-yloxyphenyl)piperazine-1-carboxamide\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC[C@H](C)[C@@H](CO)NS(=O)(=O)c1ccc(Cl)s1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][N][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][Branch1][C][C][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H36N6O3S/c1-20-19-28-26(30-21-10-12-23(13-11-21)36-17-16-33-14-5-6-15-33)31-25(20)29-22-8-7-9-24(18-22)37(34,35)32-27(2,3)4/h7-13,18-19,32H,5-6,14-17H2,1-4H3,(H2,28,29,30,31)\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1-adamantylmethyl)-3-amino-2-chlorobenzamide\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18FN3O3/c1-10-4-5-14(13(20)6-10)23-18-11-7-16(25-2)17(26-3)8-15(11)22-9-12(18)19(21)24/h4-9H,1-3H3,(H2,21,24)(H,22,23)\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCN(CCC)CCc1cccc2NC(=O)Cc12\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][Cl]\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][C][C][=C][Branch1][C][O][C][=C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 4.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C29H29N3O6S/c1-37-27-17-21(28(33)31-39(35,36)25-9-3-2-4-10-25)11-12-22(27)19-32-16-15-20-13-14-23(18-26(20)32)30-29(34)38-24-7-5-6-8-24/h2-4,9-18,24H,5-8,19H2,1H3,(H,30,34)(H,31,33)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)CN3C(=O)CCC3=O)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1nc(CSc2ccc(Cl)cc2)cc(n1)N3CCOCC3\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1cc(ccc1O)c2ccc(F)cc2F\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch2][Ring2][Ring1][C][C][N][C][C][C][S][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1][C][=C][Ring2][Ring1][=C]\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H7Cl3N2O2S3/c14-7-1-2-8(15)11(5-7)23(19,20)18-13-17-10(6-22-13)12-9(16)3-4-21-12/h1-6H,(H,17,18)\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)c1sc(cc1N)c2ccc(Cl)cc2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1C(=O)N(C)c2ncn(CC(O)CO)c2C1=O\\n\",\n        \"output\": \" -1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][=N][N][=Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H24N4O2/c1-15-4-2-6-17(12-15)22-19(24)21-14-18(16-5-3-7-20-13-16)23-8-10-25-11-9-23/h2-7,12-13,18H,8-11,14H2,1H3,(H2,21,22,24)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-chloro-n-[1-[(2r)-2,3-dihydroxypropyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(c1ccc(cc1)N(CC(F)(F)F)S(=O)(=O)c2ccccc2)(C(F)(F)F)C(F)(F)F\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 7-hydroxy-2-oxochromene-3-carboxylate\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][O][Branch2][Ring1][#C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][#Branch2][=Branch1][C][=O][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Branch1][C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[2-fluoro-5-[(4-oxo-3h-phthalazin-1-yl)methyl]phenyl]pyrrolidine-2,5-dione\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-1-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl]pyrrolidine-2-carboxamide\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@H1][C@@H1][Branch1][#Branch2][C][C][=C][N][=C][N][Ring1][Branch1][C][C][O][C][Ring1][N][=O]\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C@H1][Branch1][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-methylphenyl)quinazolin-4-amine\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-n-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide\\n\",\n        \"output\": \" -1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring2][N][N][C][=N][C][=C][Branch1][C][C][C][Branch2][Ring1][N][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C][=N][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cccc(Nc2ncnc3ccc(NC(=O)C=C)cc23)c1\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C(=C\\\\c1nn[nH]n1)/c2ccccc2\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NCC(O)(c1ccc(Cl)cc1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(4-hydroxyphenyl)acetamide\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H27N5O5S2/c31-25(19-6-8-20(9-7-19)29-15-12-26-13-16-29)28-37(34,35)22-10-11-23(24(18-22)30(32)33)27-14-17-36-21-4-2-1-3-5-21/h1-11,18,26-27H,12-17H2,(H,28,31)\\n\",\n        \"output\": \" -0.04\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Brc1ccc2OCC(=O)N(CCN3CCC(CC3)NCc4ccc5OCC(=O)Nc5n4)c2c1\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H10Cl2F3NO2/c18-12-3-1-9(5-13(12)19)8-23-14-4-2-11(17(20,21)22)6-10(14)7-15(23)16(24)25/h1-7H,8H2,(H,24,25)\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][N][=C][Branch2][Ring2][Branch2][N][C][=Branch1][C][=O][C@H1][Branch1][#Branch2][C][C][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring1][Ring1][S][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CSc1ncccc1C(=O)Nc2nccs2\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCc1c(C(=O)C(=O)N)c2c(OCC(=O)N)cccc2n1Cc3ccccc3\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][N][C][C][N][Branch2][Ring2][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C@H1][O][C][=Branch1][C][=O][C@H1][Branch1][C][C][C@@H1][Branch2][Ring1][#Branch1][O][C@H1][C][C@@][Branch1][C][C][Branch1][Ring1][O][C][C@@H1][Branch1][C][O][C@H1][Branch1][C][C][O][Ring1][O][C@H1][Branch1][C][C][C@@H1][Branch2][Ring1][Branch1][O][C@@H1][O][C@H1][Branch1][C][C][C][C@@H1][Branch1][Branch1][C@H1][Ring1][#Branch1][O][N][Branch1][C][C][C][C@][Branch1][C][C][Branch1][C][O][C][C@@H1][Branch1][C][C][\\\\C][=Branch1][=Branch2][=N][/O][C][O][C][C][O][C][\\\\C@H1][Branch1][C][C][C@@H1][Branch1][C][O][C@][Ring2][Branch1][=Branch1][Branch1][C][C][O]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)O[C@H]1CC[C@]2(C=O)[C@H]3CC[C@]4(C)[C@H](CC[C@]4(O)[C@@H]3CC[C@]2(O)C1)C5=CC(=O)OC5\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=Branch1][=N][=C][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H24ClN5O2/c1-27(2)13-18(28)14-29-19-8-6-16(7-9-19)25-21-23-11-10-20(26-21)24-17-5-3-4-15(22)12-17/h3-12,18,28H,13-14H2,1-2H3,(H2,23,24,25,26)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (5r)-3-[4-(3,6-dihydro-2h-pyran-4-yl)-3-fluorophenyl]-5-(1,2-oxazol-3-yloxymethyl)-1,3-oxazolidin-2-one\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H18N4O2S2/c1-2-11(8-21)17-13-12-14(20-16(22)24-12)19-15(18-13)23-9-10-6-4-3-5-7-10/h3-7,11,21H,2,8-9H2,1H3,(H2,17,18,19,20,22)/t11-/m1/s1\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H24N2O3/c1-13(7-8-14-5-3-2-4-6-14)21-12-18(23)15-9-10-17(22)16(11-15)19(20)24/h2-6,9-11,13,18,21-23H,7-8,12H2,1H3,(H2,20,24)\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1C(=O)c2ccccc2c3ccccc13\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][Branch1][C][Cl][Branch1][C][Cl][Cl]\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCn1c(Cc2cc(OC)c(OC)c(OC)c2)nc3c(N)ncnc13\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C7H5ClN2/c8-6-3-1-2-5-4-9-10-7(5)6/h1-4H,(H,9,10)\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" jeans\\n\",\n        \"output\": \" jeans is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H25N7O2/c1-26-12-14-27(15-13-26)21-24-19-5-3-2-4-18(19)20(25-21)23-11-10-22-16-6-8-17(9-7-16)28(29)30/h2-9,22H,10-15H2,1H3,(H,23,24,25)\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCCN1c2ccccc2Sc3ccc(Cl)cc13\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" glove\\n\",\n        \"output\": \" glove is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C][Branch1][Ring1][C][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCCc1ccc(cc1)c2nnc(N)s2\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n,n-diethyl-3-hydroxy-4-spiro[chromene-2,4'-piperidine]-4-ylbenzamide\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][Ring1][O][C][=C][N][=C][Branch1][C][C][C][C][C][N][Branch1][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=Ring1][N][C][Ring1][P][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C(N(Cc1ccccc1)c2nn[nH]n2)c3ccccc3\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch2][O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][O][C][N][C@H1][C][C][C][N][C@H1][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n,n,2-trimethylpropan-1-amine\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[3-chloro-4-(pyrazin-2-ylmethoxy)phenyl]-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H18FN3O3/c1-10-4-5-13(20)15(6-10)23-18-11-7-16(25-2)17(26-3)8-14(11)22-9-12(18)19(21)24/h4-9H,1-3H3,(H2,21,24)(H,22,23)\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][=N][N][C][C][C][N][Branch1][C][C][C][C][Ring1][Branch2][=C][N][C][=Branch1][=N][=C][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring2][Ring1][Ring1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1cc(O)c2C(=O)C(=COc2c1)c3ccc4OCOc4c3\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)-n-(2-phenylethyl)benzamide\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14O3/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10/h3-9H,1-2H3,(H,15,16)/t9-/m0/s1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S+1][Branch1][C][O-1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][Branch1][N][C][C][=C][C][Branch1][C][F][=C][C][=Ring1][#Branch1][=C][Branch1][Ring2][NH1][Ring1][N][C][C][=C][N][=C][C][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[4-chloro-2-[[(3s)-3-methyl-4-(2-phenylacetyl)piperazin-1-yl]methyl]phenyl]propanoic acid\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H14Cl2N2O3S/c1-27(25,26)13-6-7-14(17(21)11-13)19(24)23-12-5-8-16(20)15(10-12)18-4-2-3-9-22-18/h2-11H,1H3,(H,23,24)\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-tert-butyl-3-[4-[2,4-diamino-6-(phenylmethoxymethyl)pyrimidin-5-yl]phenyl]urea\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5,8-dihydroxynaphthalene-1,4-dione\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C32H41N3O4/c1-4-17-35(18-5-2)32(38)27-15-10-14-26(21-27)31(37)34-29(20-24-11-7-6-8-12-24)30(36)23-33-22-25-13-9-16-28(19-25)39-3/h6-16,19,21,29-30,33,36H,4-5,17-18,20,22-23H2,1-3H3,(H,34,37)/t29-,30+/m0/s1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O[C@@H](CNCCSCCCNCCc1cccc(Cl)c1)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCSc1nc2ccc(NC(=O)CCC(=O)O)cc2s1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-phenyl-1,3-thiazol-2-yl)pyridine-3-carboxamide\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" maple\\n\",\n        \"output\": \" maple is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)C(=O)N4CC[C@@H](C4)N(C)C)ncc2F\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-butyl-3-(4-methylphenyl)sulfonylurea\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-methyl-n-(3-pyridin-2-ylisoquinolin-1-yl)propanamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (5r)-3-[3-fluoro-4-(3-methyl-1,2-oxazol-5-yl)phenyl]-5-(triazol-1-ylmethyl)-1,3-oxazolidin-2-one\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)C[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4cc(Cl)ccc4[nH]3\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)c1cccc(c1)C(=O)Nc2ccc(C)c(NC(=O)c3ccc(O)cc3)c2\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" freckle\\n\",\n        \"output\": \" freckle is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-amino-6-[3-fluoro-4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-pyridin-3-ylpyrazine-2-carboxamide\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H13N5S/c1-21-9-20-13(10-5-3-2-4-6-10)14(21)12-7-11-15(17)18-8-19-16(11)22-12/h2-9H,1H3,(H2,17,18,19)\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][C][O][C][NH1][C][=C][C][Branch1][C][C][=C][Branch2][Ring1][C][C][=C][Ring1][#Branch1][C][=Ring1][#Branch2][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H11NO4/c1-2-15-9-6-4-3-5-8(9)13-12(14(15)18)10(16)7-11(17)19-13/h3-7,17H,2H2,1H3\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H11NO2/c16-13-14(17,10-6-2-1-3-7-10)11-8-4-5-9-12(11)15-13/h1-9,17H,(H,15,16)\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H8N4O/c9-12-7-8(13)11-6-4-2-1-3-5(6)10-7/h1-4H,9H2,(H,10,12)(H,11,13)\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1cccc(c1)c2cnc3ccc(NC4CCOCC4)nn23\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H15ClFN3O3/c1-25-15-6-10-14(7-16(15)26-2)22-8-11(18(21)24)17(10)23-9-3-4-13(20)12(19)5-9/h3-8H,1-2H3,(H2,21,24)(H,22,23)\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)NCC(O)COc1ccccc1CC=C\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H17N3S/c1-2-3-4-5-10-6-8-11(9-7-10)12-15-16-13(14)17-12/h6-9H,2-5H2,1H3,(H2,14,16)\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1cc(cc(c1)[N+](=O)[O-])[N+](=O)[O-]\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[[9-chloro-7-(2,6-difluorophenyl)-5h-pyrimido[5,4-d][2]benzazepin-2-yl]amino]benzoic acid\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COCCOc1nc(N)c2NC(=O)N(Cc3cccc(CC(=O)OC)c3)c2n1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H18ClNO2/c17-14-5-3-11(4-6-14)15(19)12-7-9-18(10-8-12)16(20)13-1-2-13/h3-6,12-13H,1-2,7-10H2\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" beaver\\n\",\n        \"output\": \" beaver is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1(C)CCC(CC1)NC(=O)[C@@H](N)CCC(=O)O\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(ccc1Cn2ccc3ccc(NC(=O)OC4CCCC4)cc23)C(=O)O\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc(NC(=O)c2ccc(O)cc2)cc1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch2][Ring1][#Branch1][C][C][O][C][=C][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][Ring1][O][C][C][C][=C][C][=C][Branch1][#Branch2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][Ring1][O]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(3,4-dimethoxyphenyl)-5,7-dihydroxychromen-4-one\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H5FN2S/c8-4-1-2-5-6(3-4)11-7(9)10-5/h1-3H,(H2,9,10)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][C][O][=C][C][O][C][=C][Branch1][#Branch2][C][=Branch1][C][=O][C][Ring1][N][=Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-(4-methoxybenzoyl)pyrrolidin-2-one\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H21ClN4O4/c19-14-6-5-12(23-17(26)22-15(24)10-21-23)9-13(14)16(25)20-11-18(27)7-3-1-2-4-8-18/h5-6,9-10,27H,1-4,7-8,11H2,(H,20,25)(H,22,24,26)\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H20N2O5S2/c1-13(2)26-16-10-14(19(23)22-20-21-8-9-28-20)11-17(12-16)27-15-4-6-18(7-5-15)29(3,24)25/h4-13H,1-3H3,(H,21,22,23)\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C(C1NCCc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H16O4/c1-11-15-9-8-14(21-3)10-16(15)22-18(19)17(11)12-4-6-13(20-2)7-5-12/h4-10H,1-3H3\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H12N4O/c1-10-8-15-18-19-16(21)20(15)14-9-12(2-3-13(10)14)11-4-6-17-7-5-11/h2-9H,1H3,(H,19,21)\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C][Branch1][Ring1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(F)cccc34\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=O][N][C][C][C@@H1][C][C][C][=C][C][=C][O][C][C][C][Ring1][Branch1][=C][Ring1][N][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-aminophenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Cc1ccccc1)Nc2nccs2\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2nc(Nc3ccc(C(=O)NCCN(C)C)c(F)c3)ncc2F\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H17N3O5S/c1-7-6-25-15-11(14(22)19(15)12(7)16(23)24)18-13(21)10(17)8-2-4-9(20)5-3-8/h2-5,10-11,15,20H,6,17H2,1H3,(H,18,21)(H,23,24)/t10-,11-,15-/m1/s1\\n\",\n        \"output\": \" -0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H14F3N5/c13-12(14,15)11-17-16-9-5-6-10(18-20(9)11)19-7-3-1-2-4-8-19/h5-6H,1-4,7-8H2\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H31ClN4O5/c1-32-8-4-17(5-9-32)14-34-19-12-21-24(23(13-19)37-18-6-10-33-11-7-18)27(30-15-29-21)31-25-20(28)2-3-22-26(25)36-16-35-22/h2-3,12-13,15,17-18H,4-11,14,16H2,1H3,(H,29,30,31)\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-azabicyclo[2.2.2]octan-8-yl 2-hydroxy-2,2-di(phenyl)acetate\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(ccc1Cn2cnc3ccc(NC(=O)CC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-methyl-n-(5-methyl-1,3-thiazol-2-yl)-1,1,4-trioxo-3h-benzo[e]thiazine-3-carboxamide\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-(3-methyl-5-phenylimidazol-4-yl)thieno[3,2-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-7-[(1-methylpiperidin-4-yl)methoxy]-5-(oxan-4-yloxy)quinazolin-4-amine\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H12O4/c1-19-14-5-3-2-4-11(14)13-9-20-15-8-10(17)6-7-12(15)16(13)18/h2-9,17H,1H3\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Nc1ccncc1)c2cccc3ccccc23\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-hydrazinyl-1h-quinoxalin-2-one\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[1-methyl-5-(4-methylbenzoyl)pyrrol-2-yl]acetic acid\\n\",\n        \"output\": \" -1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H17F3N2O2/c1-12-3-6-19-17(9-12)21(13(2)27(19)11-20(28)29)16-7-8-26-18-10-14(22(23,24)25)4-5-15(16)18/h3-10H,11H2,1-2H3,(H,28,29)\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C@@H1][Branch1][O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1OC)C2=COc3cc(O)cc(O)c3C2=O\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H16N4/c1-2-7-13-12(6-1)18-16(19-13)10-5-11-17-20-14-8-3-4-9-15(14)21-17/h1-4,6-9H,5,10-11H2,(H,18,19)(H,20,21)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H11ClF3NO4S/c1-10(18,11(13,14)15)9(17)16-8-4-3-6(5-7(8)12)21(2,19)20/h3-5,18H,1-2H3,(H,16,17)/t10-/m1/s1\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][C][Ring1][=Branch2][=N][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Ring1][S][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][N][C][C][O][C][Ring1][Branch1][=N][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)S(=O)(=O)c2ccc(cc2)c3cnc(N)c(n3)C(=O)Nc4cnccc4CN5CCCC5\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(C)c4Cl\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)NCC(O)COc1ccccc1OCC=C\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(2-fluoro-4-methylphenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20F3N3O3/c1-11(2)16(17(27)19(20,21)22)24-15(26)10-25-14(9-8-13(23)18(25)28)12-6-4-3-5-7-12/h3-9,11,16H,10,23H2,1-2H3,(H,24,26)\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H12Cl2N4/c1-10-21-22-16-9-20-17(12-4-2-3-5-14(12)19)13-8-11(18)6-7-15(13)23(10)16/h2-8H,9H2,1H3\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H20N4O3S2/c1-12-13(2)28-18-16(12)17(20-11-21-18)27-10-15(24)22-5-7-23(8-6-22)19(25)14-4-3-9-26-14/h3-4,9,11H,5-8,10H2,1-2H3\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@@H1][Branch1][C][O][C@@H1][C@H1][C@@H1][Branch1][C][C][C][=Branch2][Ring1][=C][=C][Branch1][Branch2][N][Ring1][=Branch1][C][Ring1][Branch2][=O][C][=Branch1][C][=O][O][C][O][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][C][S][C][C][N][Branch1][Ring2][C][Ring1][Ring2][C][=N][C][C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-fluoro-n-[(1s)-1-(5-fluoropyrimidin-2-yl)ethyl]-n'-(5-methyl-1h-pyrazol-3-yl)pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H12O3/c1-10-15(11-5-3-2-4-6-11)16(18)13-8-7-12(17)9-14(13)19-10/h2-9,17H,1H3\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2][C][=C][C][=C][Branch2][Ring1][N][C][C@H1][Branch2][Ring1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][=Branch1][C][=O][O][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H14O4/c1-13-9-4-2-3-5-10(9)14-7-8(12)6-11/h2-5,8,11-12H,6-7H2,1H3\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)(C)c1ccc(cc1)C(O)CCCN2CCC(CC2)C(O)(c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(Cl)c(c1)S(=O)(=O)Nc2nccs2\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CSc1ncccc1C(=O)NCC2CCCCC2\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCN(CCNC[C@H](O)c1ccc(O)c2NC(=O)Sc12)C(=O)CCOCCc3ccccc3\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][O][N][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][C][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=N]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][N][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][O][C][=C][C][=C][N][=C][Ring1][=Branch1][N][=Ring1][=Branch2]\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H14N2/c1-2-4-13-11-16(10-7-12(13)3-1)14-5-8-15-9-6-14/h1-6,8-9H,7,10-11H2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-methyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCn1c2ccccc2c3cc(NC(=O)CN(C)C)ccc13\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H31NO5/c1-18-6-10-20(11-7-18)26(31)33-24-15-14-22(23(30)17-29-28(3,4)5)16-25(24)34-27(32)21-12-8-19(2)9-13-21/h6-16,23,29-30H,17H2,1-5H3\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H5F2NO4S/c12-11(13)17-6-2-1-5(3-7(6)18-11)4-8-9(15)14-10(16)19-8/h1-4H,(H,14,15,16)/b8-4-\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-hydroxy-3-(4-hydroxyphenyl)chromen-2-one\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H](C(=O)O)c1cccc(c1)C(=O)c2ccccc2\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=C][N][C][Ring1][Branch1][=S]\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccccc1Nc2oc(nn2)C(=O)Nc3ccc(N4CCOCC4)c(F)c3\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H16N4O2/c1-19-12-10-16-13(11-4-2-3-5-15-11)17-14(12)18-6-8-20-9-7-18/h2-5,10H,6-9H2,1H3\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(CN2C(=O)NC3=C(C=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C3=O)c4ccccc4)C2=O)cc1\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][N][C][=Branch1][C][=O][N][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H20N2O2/c1-3-15(4-2)9-10-17-13(16)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10,14H2,1-2H3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4,6-dimethylpyrimidin-2-yl)sulfanyl-n-(5-methyl-1,2-oxazol-3-yl)acetamide\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)benzamide\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H19N3O3S/c1-15(24)22-18-6-8-20(9-7-18)27(25,26)23-19-4-2-16(3-5-19)14-17-10-12-21-13-11-17/h2-13,23H,14H2,1H3,(H,22,24)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(Br)cc1C(=O)C(=O)c2cc(Br)ccc2O\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" scent\\n\",\n        \"output\": \" scent is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1C(=O)C(=Cc2cnc(NC3CCOCC3)nc12)Oc4ccc(F)cc4F\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(C(=O)c1cccnc1)c2cccnc2\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-chloro-4-methyl-2-pyridin-2-yl-6-pyrrolidin-1-ylpyrimidine\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-phenyl-2-phenylsulfonylethanone\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H24BrF2N5O3S/c21-12-9-14(22)13(15(23)10-12)11-31-18-16(17(24)29)19(32-27-18)26-20(30)25-5-1-2-6-28-7-3-4-8-28/h9-10H,1-8,11H2,(H2,24,29)(H2,25,26,30)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-propyl-2-(5-pyrrolidin-1-ylsulfonylpyridin-2-yl)sulfanylacetamide\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H14N2O/c1-2-6-12-11(4-1)5-3-7-13(12)17-10-14-15-8-9-16-14/h1-7H,8-10H2,(H,15,16)\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][N][=C][Branch1][S][C][C][S][C][C][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1][S][Ring1][S]\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-dimethylaminoethyl)-2-fluoro-4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C@H1][Branch1][C][N][C][=Branch1][C][=O][O][C][C][O][C][N][C][=N][C][C][=Branch1][C][=O][N][=C][Branch1][C][N][N][C][Ring1][O][=Ring1][Branch2]\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccccc1NC(=O)N[C@H]2N=C(c3ccccc3)c4ccccc4NC2=O\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch2][Ring1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=C][Ring1][#Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][Branch1][C][C][N][=C][Ring1][#Branch1][O][C]\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-1-morpholin-4-yl-2-[4-[[1-(1,3-thiazol-4-ylmethyl)indazol-5-yl]amino]quinazolin-5-yl]oxypropan-1-one\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H21N5O2/c1-11-16(12(2)23-18(19-11)20-13(3)22-23)9-10-17(24)21-14-5-7-15(25-4)8-6-14/h5-8H,9-10H2,1-4H3,(H,21,24)\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12N2OS/c1-9-8-13-12(16-9)14-11(15)7-10-5-3-2-4-6-10/h2-6,8H,7H2,1H3,(H,13,14,15)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC1=NC(Nc2cccc(F)c12)c3cccs3\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[[5-[2-[(2r,6s)-2,6-dimethylmorpholin-4-yl]-4-morpholin-4-ylpyrido[5,6-e]pyrimidin-7-yl]-2-methoxyphenyl]methylamino]ethanol\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H28N2O/c1-3-25(4-2)23(26)21-12-10-19(11-13-21)22(18-8-6-5-7-9-18)20-14-16-24-17-15-20/h5-13,24H,3-4,14-17H2,1-2H3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](C)[C@H](N)C1=N[C@@H](CS1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(=O)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H]2CCCCNC(=O)[C@H](CC(=O)N)NC(=O)[C@@H](CC(=O)O)NC(=O)[C@H](Cc3cnc[nH]3)NC(=O)[C@@H](Cc4ccccc4)NC(=O)[C@@H](NC(=O)[C@@H](CCCN)NC2=O)[C@@H](C)CC\\n\",\n        \"output\": \" -0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H6N2O2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H,7H2\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COC(=O)c1cccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)c1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(2-phenylethylamino)propylsulfanyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNCC[C@@H](Oc1ccccc1C)c2ccccc2\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(phenylmethyl)indole-3-carboxylic acid\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cccc(NC(=O)NCC(N2CCOCC2)c3cccnc3)c1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[(z)-(5-fluoro-2-oxo-1h-indol-3-ylidene)methyl]-n-[(2s)-2-hydroxy-3-morpholin-4-ylpropyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(phenoxy)-n-(pyridin-2-ylmethyl)benzamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C@H1][C][C@H1][Branch1][=Branch2][C@H1][Branch1][C][O][C@@H1][Ring1][=Branch1][O][N][N][=N][C][=C][Branch2][Ring1][Branch1][N][C@@H1][C][C@H1][Ring1][Ring1][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2][N][=C][Branch1][N][S][C][C][C][Branch1][C][F][Branch1][C][F][F][N][=C][Ring2][Ring1][N][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(O)(C(=O)Nc1ccc2c(c1)c3ccccc3S2(=O)=O)C(F)(F)F\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H22ClN5O4/c1-23(2,3)27-22(33)25-14-6-4-5-12(9-14)11-29-21(32)17-18(20(31)28-29)26-16-10-13(24)7-8-15(16)19(17)30/h4-10H,11H2,1-3H3,(H,26,30)(H,28,31)(H2,25,27,33)\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C(=O)N1CCC(CC1)N2CCC(CC2)Oc3ccc(Cl)c(Cl)c3)S(=O)(=O)c4ccc(C)cc4\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-n-(cyclohexylmethyl)-5-(3,5-dioxo-1,2,4-triazin-2-yl)benzamide\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(NC(=O)c2ccnc(N)n2)cc1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC[C@H](CO)Nc1nc(SCc2ccccc2)nc3NC(=O)Sc13\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H12O5/c1-20-11-4-2-9(3-5-11)12-8-21-14-7-10(17)6-13(18)15(14)16(12)19/h2-8,17-18H,1H3\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-aminophenyl)-4-[5-(azetidin-1-ylmethyl)-3-fluoropyridin-2-yl]benzamide\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(2-phenylethoxy)aniline\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(\\\\C=C/2\\\\SC(=O)NC2=O)cc(OC)c1O\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@@H1][Branch1][#C][C][=Branch1][C][=O][N][C][C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][Branch1][P][O][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][=C]\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H34ClN3O2/c26-23-2-1-16(12-29-13-20-10-27-11-21(14-29)31-20)6-22(23)24(30)28-15-25-7-17-3-18(8-25)5-19(4-17)9-25/h1-2,6,17-21,27H,3-5,7-15H2,(H,28,30)\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H11NO5S/c1-17-7-3-6(4-8(18-2)10(7)14)5-9-11(15)13-12(16)19-9/h3-5,14H,1-2H3,(H,13,15,16)/b9-5+\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H19N5O/c1-13-4-2-5-18(25-13)21-20(19-6-3-11-27(19)26-21)15-9-10-24-17-8-7-14(22(23)28)12-16(15)17/h2,4-5,7-10,12H,3,6,11H2,1H3,(H2,23,28)\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H35NO2/c1-3-20(4-2)15-16-22-18(21)19(13-9-6-10-14-19)17-11-7-5-8-12-17/h17H,3-16H2,1-2H3\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=N][N][=C][C][=C][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][=Branch1][N][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H9NO/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H23ClN4O3/c1-3-5-6-12(4-2)10-20-17(25)14-9-13(7-8-15(14)19)23-18(26)22-16(24)11-21-23/h7-9,11-12H,3-6,10H2,1-2H3,(H,20,25)(H,22,24,26)\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][Branch2][C][N][C][C][C][Ring1][Ring2][=C][N][=C][Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N]\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][=N][C][=C][Branch1][#C][C][=C][C][=C][O][C][C][O][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][Ring1][#C][C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)c1cccc2c(cccc12)S(=O)(=O)N\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H22N2O3S2/c1-25(22,23)15-8-6-14(7-9-15)16(12-13-4-2-3-5-13)17(21)20-18-19-10-11-24-18/h6-11,13,16H,2-5,12H2,1H3,(H,19,20,21)/t16-/m1/s1\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=C][C][Branch1][C][Cl][=C][Branch2][Ring1][Branch1][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][Ring1][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-cyclopentyl-2-(2-hydroxyphenoxy)acetamide\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOC(=O)c1ccc(OCCC2CCN(CC2)c3ccc(C)nn3)cc1\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccc(N=Nc2ccccc2)c(N)n1\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H28ClN3O3S2/c23-16-4-1-3-15(13-16)7-9-24-10-12-30-11-2-8-25-14-19(28)17-5-6-18(27)20-21(17)31-22(29)26-20/h1,3-6,13,19,24-25,27-28H,2,7-12,14H2,(H,26,29)/t19-/m0/s1\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][=C][C][=C][NH1][C][=C][Branch1][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H32N6/c1-3-32-13-15-33(16-14-32)18-21-9-11-23(12-10-21)25-17-24-26(28-19-29-27(24)31-25)30-20(2)22-7-5-4-6-8-22/h4-12,17,19-20H,3,13-16,18H2,1-2H3,(H2,28,29,30,31)/t20-/m1/s1\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16N2O3/c1-10-11(6-7-16(20)21)9-18-15(10)8-13-12-4-2-3-5-14(12)19-17(13)22/h2-5,8-9,18H,6-7H2,1H3,(H,19,22)(H,20,21)/b13-8-\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H20N2O2/c1-11(2,3)10(15)13-8-6-4-5-7-12-9(8)14/h8H,4-7H2,1-3H3,(H,12,14)(H,13,15)/t8-/m0/s1\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1cnc(NC(=O)C(CC2CCOCC2)c3ccc(cc3)S(=O)(=O)C4CC4)s1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)NC[C@@H](C(=O)N1CCN(CC1)c2ncnc3[C@H](O)C[C@@H](C)c23)c4ccc(Cl)cc4\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" name\\n\",\n        \"output\": \" name is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H13FN2O4/c1-21-14(19)9-22-13-7-2-10(8-17-13)15(20)18-12-5-3-11(16)4-6-12/h2-8H,9H2,1H3,(H,18,20)\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccccc1NC(=O)c2ccccn2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(C(=O)Nc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" bike\\n\",\n        \"output\": \" bike is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][=C][C][=C][N][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H27N5O3/c1-27(2)13-18(28)14-30-20-10-6-17(7-11-20)26-22-12-21(23-15-24-22)25-16-4-8-19(29-3)9-5-16/h4-12,15,18,28H,13-14H2,1-3H3,(H2,23,24,25,26)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H19N/c15-14-9-6-13(7-10-14,8-11-14)12-4-2-1-3-5-12/h1-5H,6-11,15H2\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H9N5/c10-8-11-6-12-9(14-8)13-7-4-2-1-3-5-7/h1-6H,(H3,10,11,12,13,14)\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][Branch1][=C][\\\\C][=C][\\\\C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][#C]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(2-chlorophenyl)-n-cyclohexylpiperazine-1-carboxamide\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)C(=O)c1ccc(cc1)C(=C2CCNCC2)c3ccc(Cl)c(Cl)c3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][N][C][=N][C][=C][S][Ring1][Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (e)-n-methyl-n-[(3-methyl-1-benzofuran-2-yl)methyl]-3-(7-oxo-6,8-dihydro-5h-1,8-naphthyridin-3-yl)prop-2-enamide\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H28N6O5S/c1-13(2)9-29-22-19(20(32)27(4)24(29)34)18(21(33)30-10-14(31)12-35-30)17(36-22)11-28-16-8-6-5-7-15(16)26-23(28)25-3/h5-8,13-14,31H,9-12H2,1-4H3,(H,25,26)/t14-/m0/s1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H10Cl2N2O4/c17-12-3-1-9(5-13(12)18)8-19-14-4-2-11(20(23)24)6-10(14)7-15(19)16(21)22/h1-7H,8H2,(H,21,22)\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch2][Ring1][O][C][O][C][=Branch1][C][=O][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][N][Branch1][=Branch1][N][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H31NO4/c1-14(2)19-11-17(20)13-23-18-7-5-16(6-8-18)12-21-9-10-22-15(3)4/h5-8,14-15,17,19-20H,9-13H2,1-4H3\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-hydroxy-1,2-di(phenyl)propan-1-one\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H31N5O4/c1-16-13-30(14-17(2)34-16)25-27-23-20(24(28-25)29-8-10-33-11-9-29)5-6-21(26-23)18-4-7-22(32-3)19(12-18)15-31/h4-7,12,16-17,31H,8-11,13-15H2,1-3H3/t16-,17+\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCCC1CCOC(C)(c2ccccc2)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H30Cl2N2O3/c26-22-7-6-21(16-23(22)27)32-20-10-12-28(13-11-20)17-18-8-14-29(15-9-18)24(25(30)31)19-4-2-1-3-5-19/h1-7,16,18,20,24H,8-15,17H2,(H,30,31)\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-amino-n-(4-methylpyrimidin-2-yl)benzenesulfonamide\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][=C]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-1h-imidazole\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Nc1cccnc1C(=O)NCC2CCOCC2)c3cccc4ccccc34\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-6-methoxy-1,4-benzothiazin-3-one\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=C][O][C][C][Branch1][C][O][C][N][C][Branch1][C][C][C][C][=Branch1][Ring2][=C][Ring1][#C][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H26ClN5O4/c28-21-13-18(9-10-23(21)36-15-19-5-1-2-11-29-19)32-27-26-22(30-17-31-27)7-3-8-24(26)37-16-20-6-4-12-33(20)25(35)14-34/h1-3,5,7-11,13,17,20,34H,4,6,12,14-16H2,(H,30,31,32)/t20-/m1/s1\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][C][N][Branch2][Ring2][=Branch2][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][=C][N][C@H1][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][N][=C][Ring1][#C][NH1][Ring2][Ring1][C][C][C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][O][C][=Branch1][C][=O][C][=C][C][Ring1][#Branch1][=C][C][C][=C][O][C][Ring1][=C][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H18ClN3O/c1-2-18-5-7-19(8-6-18)15(20)14-10-11-9-12(16)3-4-13(11)17-14/h3-4,9-10,17H,2,5-8H2,1H3\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][C][=C][Branch1][#Branch2][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][C][=C][S][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl 4-methyl-3-[(1-methyl-3-oxo-2,1-benzothiazol-5-yl)sulfonylamino]benzoate\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [6-(oxan-4-ylmethylcarbamoyl)-5-[[4-(triazol-1-ylmethyl)naphthalene-1-carbonyl]amino]pyridin-2-yl] 3,3,3-trifluoropropane-1-sulfonate\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H16ClN3O3/c1-24-15-7-12-14(8-16(15)25-2)21-9-13(18(20)23)17(12)22-11-5-3-4-10(19)6-11/h3-9H,1-2H3,(H2,20,23)(H,21,22)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H18N2O4S/c1-16(2)13-8-4-7-12-11(13)6-5-9-14(12)22(20,21)17(3)10-15(18)19/h4-9H,10H2,1-3H3,(H,18,19)\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C@H1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(C1CCN(CCC(C2CCN(CC2)S(=O)(=O)CC)c3ccccc3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOCc1nc2c(N)nc3ccccc3c2n1CC(C)(C)O\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H8N2OS2/c1-6(12)10-9-11-7(5-14-9)8-3-2-4-13-8/h2-5H,1H3,(H,10,11,12)\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H30Cl2N4O/c1-15(2)26-7-3-4-16(14-26)13-24-8-10-25(11-9-24)20(27)23-17-5-6-18(21)19(22)12-17/h5-6,12,15-16H,3-4,7-11,13-14H2,1-2H3,(H,23,27)/t16-/m0/s1\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H24ClFN4O2/c1-28-7-3-4-14(11-28)12-30-21-10-19-16(9-20(21)29-2)22(26-13-25-19)27-18-6-5-15(23)8-17(18)24/h5-6,8-10,13-14H,3-4,7,11-12H2,1-2H3,(H,25,26,27)/t14-/m1/s1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" propan-2-yl 4-[6-(2-fluoro-4-methylsulfonylphenoxy)-5-methylpyrimidin-4-yl]oxypiperidine-1-carboxylate\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(2,3-dihydro-1,4-benzodioxin-7-yl)-6,7-dihydro-5h-pyrrolo[1,2-a]imidazole\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][=N][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=C][C][Branch1][#C][N][C][=C][C][=C][C][O][C][O][C][Ring1][=Branch2][=Ring1][Branch1][=N][C][=N][C][Ring1][S][=C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-[1-hydroxy-4-[4-[hydroxy-di(phenyl)methyl]piperidin-1-yl]butyl]phenyl]-2-methylpropanoic acid\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C(N1CCN(CC1)c2nc3ccccc3s2)c4nnnn4Cc5cccs5\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" ON1C(=O)N(CC2COc3ccccc3O2)c4ccsc4C1=O\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H17Cl2N5O/c1-17(2)23-15(20)22-16(21)24(17)11-5-8-14(13(19)9-11)25-12-6-3-10(18)4-7-12/h3-9H,1-2H3,(H4,20,21,22,23)\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16FN5O3S3/c1-7-13(27-16(20-7)21-9(3)23)11-5-12(14(17)18-6-11)22-28(24,25)15-8(2)19-10(4)26-15/h5-6,22H,1-4H3,(H,20,21,23)\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(4-fluorophenyl)-3h-imidazol-2-amine\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-phenylpiperidine\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][C][Branch1][=Branch1][S][C][C][C][O][=C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][S][C][Ring2][Ring1][N][=Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H29ClFN3O4/c1-30-21-13-19(26)18(24)12-17(21)23(29)27-20-8-10-28(14-22(20)31-2)9-3-11-32-16-6-4-15(25)5-7-16/h4-7,12-13,20,22H,3,8-11,14,26H2,1-2H3,(H,27,29)/t20-,22+/m1/s1\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H23FN4O2/c1-11-17(23-12(2)18(11)20(27)22-7-8-25(3)4)10-15-14-9-13(21)5-6-16(14)24-19(15)26/h5-6,9-10,23H,7-8H2,1-4H3,(H,22,27)(H,24,26)/b15-10-\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" [O-][N+](=O)c1ccc2NC(=O)CN=C(c3ccccc3Cl)c2c1\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][Branch1][N][N][C][C][N][C][Branch1][C][C][C][Ring1][#Branch1][C][Branch1][C][F][=C][Ring2][Ring1][#Branch1][Ring1][#C]\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch2][Ring1][Ring2][O][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-cyclohexyl-2-methyl-5-oxo-1-(thiophen-2-ylmethyl)pyrrolidine-2-carboxamide\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H12N2O3S2/c1-13-10-5-4-8(6-9(10)11(14)17-13)18(15,16)12-7-2-3-7/h4-7,12H,2-3H2,1H3\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H19F3N2O4S/c1-4-19(5-2)24(22,23)11-8-6-10(7-9-11)18-12(20)13(3,21)14(15,16)17/h6-9,21H,4-5H2,1-3H3,(H,18,20)\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H26F3N5O4/c1-16(2)22(23(36)26(27,28)29)33-21(35)15-34-20(18-6-4-3-5-7-18)9-8-19(24(34)37)32-25(38)31-14-17-10-12-30-13-11-17/h3-13,16,22H,14-15H2,1-2H3,(H,33,35)(H2,31,32,38)\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H29NO3/c1-14(2)19-11-17(20)13-22-18-7-5-15(6-8-18)9-10-21-12-16-3-4-16/h5-8,14,16-17,19-20H,3-4,9-13H2,1-2H3\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,2,2-trifluoro-n-[4-(2-methoxyphenoxy)phenyl]-n-(pyridin-3-ylmethyl)ethanesulfonamide\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1cc(sc1N)c2ccccc2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H26ClNO4S/c1-3-6-17-20(9-8-16-19(4-2)25-29-23(16)17)28-11-5-12-30-21-10-7-15(13-18(21)24)14-22(26)27/h7-10,13H,3-6,11-12,14H2,1-2H3,(H,26,27)\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=Branch2][Ring1][=Branch2][=C][C][=C][N][=C][Branch1][O][N][C][Branch1][Ring2][C][C][O][C][C][O][N][=C][Ring2][Ring1][Ring1][Ring1][=C][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][Branch2][Ring1][O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][C][Branch1][C][C][C][N][=C][Branch1][#Branch2][N][=C][Ring2][Ring1][Ring2][O][C][C][O][C][=N][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C32H37F3N2O5S2/c1-4-37(31(38)19-22-5-9-26(10-6-22)43(2,39)40)25-13-16-36(17-14-25)18-15-28(24-20-29(33)32(35)30(34)21-24)23-7-11-27(12-8-23)44(3,41)42/h5-12,20-21,25,28H,4,13-19H2,1-3H3/t28-/m1/s1\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)NC(=O)C(Nc1ccc2CCCc2c1)c3ccccc3\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H13ClFNO2/c1-9-5-6-13(10(7-9)8-14(19)20)18-15-11(16)3-2-4-12(15)17/h2-7,18H,8H2,1H3,(H,19,20)\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[1-hydroxy-2-[1-(phenoxy)propan-2-ylamino]propyl]phenol\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H16N2O2S/c1-7(2)11-5-8(12)6-13-9-10-3-4-14-9/h3-4,7-8,11-12H,5-6H2,1-2H3\\n\",\n        \"output\": \" -0.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][=N][C][Branch1][Ring1][O][C][=N][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H21F3N6O2/c19-18(20,21)13-9-15(22)23-11-12(13)14-10-16(26-1-5-28-6-2-26)25-17(24-14)27-3-7-29-8-4-27/h9-11H,1-8H2,(H2,22,23)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][N][Branch1][C][C][C][=Branch1][C][=O][C@@][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][C][N][Branch1][Ring2][C][Ring1][=N][C][=Branch1][C][=O][C@@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][N]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring2][C][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=C][Branch2][Ring1][C][C][Branch1][N][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][S][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][C][C][C][Ring1][Ring1][C][=C][Ring1][N]\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C][C][Ring1][Branch1][C][C][Branch1][Ring2][C][Ring1][#Branch1][O][C][=Branch1][C][=O][C][Branch1][Ring1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" methyl n-[2-(4-fluorophenyl)-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H20N2O2/c1-13-7-8-19-18(11-13)21(15(3)24(19)12-20(25)26)16-9-10-23-22-14(2)5-4-6-17(16)22/h4-11H,12H2,1-3H3,(H,25,26)\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][#Branch1][C][N][C][=Branch1][C][=O][C][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][=N][Ring1][#Branch1][C][=C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O-1][S+1][Branch2][Ring2][C][C][C][C][C][=Branch1][C][=O][N][Branch1][S][N][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][N][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)CN=C(c2ccccc2F)c3cc(ccc13)[N+](=O)[O-]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-n-(3-morpholin-4-ylpropyl)furan-2-carboxamide\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)COc1ccc(cc1c2ccccc2)[N+](=O)[O-]\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(4-chlorophenyl)-2-phenyl-n-(1-propan-2-ylpiperidin-4-yl)acetamide\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(COC(=O)N2CCC(CNc3ncccn3)CC2)cc1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (6s)-n'-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][C][O][C][C][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)CCOCCOC(=O)C1(CCCC1)c2ccccc2\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][O][N][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][N][=N][Ring1][#C]\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H20N4O3/c1-26-16-8-9-18(27-2)14(12-16)13-23-20-19-17(24-25-20)10-11-22-21(19)28-15-6-4-3-5-7-15/h3-12H,13H2,1-2H3,(H2,23,24,25)\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Branch1][Ring2][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][=C][Ring1][#Branch2][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCNC(=O)c1nnc2c(cccc2c1N)c3cncc(c3)C(=O)N4CCC4\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H29N5O2/c1-26(14-32-15-26)16-33-20-6-7-22-21(13-20)28-17-31(22)24-8-5-18-3-2-4-23(25(18)29-24)30-11-9-19(27)10-12-30/h2-8,13,17,19H,9-12,14-16,27H2,1H3\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H17NO4/c25-21(14-28-13-15-6-2-1-3-7-15)24-16-10-11-18-17-8-4-5-9-19(17)22(26)23(27)20(18)12-16/h1-12H,13-14H2,(H,24,25)\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H5F3N6/c10-9(11,12)8-15-14-6-1-2-7(16-18(6)8)17-4-3-13-5-17/h1-5H\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H24BrFN4O2/c1-28-7-3-4-14(11-28)12-30-21-10-19-16(9-20(21)29-2)22(26-13-25-19)27-18-6-5-15(23)8-17(18)24/h5-6,8-10,13-14H,3-4,7,11-12H2,1-2H3,(H,25,26,27)/t14-/m1/s1\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(phenylmethoxy)aniline\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(2,2-dicyclohexylethyl)piperidine\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H](NC(=O)C)c1ccc(Nc2ncc3cc(ccc3n2)c4ccncc4)cc1\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCNC1=Nc2ccccc2C(=NC1c3cccs3)c4ccccc4\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][S][C][=Branch1][=Branch1][=C][C][=Ring1][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-phenyl-7-(2,4,5-trimethyl-3,6-dioxo-1-cyclohexa-1,4-dienyl)heptanoic acid\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1c(ccnc1N2CCNCC2)C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][N][C][C][=C][C][=C][Branch1][=Branch2][\\\\C][=C][\\\\C][=Branch1][C][=O][N][O][C][=C][Ring1][N]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(2-chloro-3-fluorophenyl)-1-(4-chloro-2-hydroxy-3-piperazin-1-ylsulfonylphenyl)urea\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1C(C)C)NC(=O)OCc2ccccc2)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-amino-2-(4-bromobenzoyl)-4-methyl-7h-thieno[3,2-e]pyridin-6-one\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCc1nc2c(N)nc3ccccc3c2n1CC(C)C\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H15N3O6S3/c21-28(22,20-17-18-7-10-27-17)13-3-1-12(2-4-13)19-29(23,24)14-5-6-15-16(11-14)26-9-8-25-15/h1-7,10-11,19H,8-9H2,(H,18,20)\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[(2,6-difluorophenyl)methylsulfonyl]-4-[3-(trifluoromethyl)pyridin-2-yl]piperazine\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(=O)Nc1ccc(c(c1)C(F)(F)F)[N+](=O)[O-]\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H13N3S/c1-2-5-10-16-11-12(17-10)8-6-3-4-7-9(8)15-13(11)14/h3-4,6-7H,2,5H2,1H3,(H2,14,15)\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-n-[(1-hydroxycycloheptyl)methyl]-5-[4-[(2s)-2-hydroxy-3-methoxypropyl]-3,5-dioxo-1,2,4-triazin-2-yl]benzamide\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [4-(1,3-benzodioxol-5-ylmethyl)piperazin-1-yl]-[1-(5-pyrrol-1-yl-1,3,4-thiadiazol-2-yl)piperidin-4-yl]methanone\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(cc1)C(=O)N2CCC[C@@H](C2)c3onc(n3)c4ccc(F)cc4\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(2-fluorophenyl)amino]-n-(6-pyridin-3-yloxypyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(O)(C(=O)Nc1ccc(cc1)S(=O)(=O)c2ccc(F)cc2)C(F)(F)F\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H14F3N3O3S/c1-26-16-7-2-10(8-13(16)18)15-9-14(17(19)20)22-23(15)11-3-5-12(6-4-11)27(21,24)25/h2-9,17H,1H3,(H2,21,24,25)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=C][Branch1][C][O][C][=Branch2][Ring1][N][=C][C][=C][Ring1][#Branch1][O][C][C][C][S][C][=C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][Ring1][#Branch2][Cl][C][=Branch1][C][=O][C][C]\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3-methylphenyl)quinazolin-4-amine\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3cc(C)nc(C)c3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-phenylspiro[1h-2-benzofuran-3,4'-piperidine]\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-cyclohexyl-2-phenylsulfanylpyridine-3-carboxamide\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O]\\n\",\n        \"output\": \" -1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-methyl-3-phenylpyrrolidine-2,5-dione\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H13BrN2O/c1-17-10-6-4-9(5-7-10)12-13(14)16-8-2-3-11(16)15-12/h4-7H,2-3,8H2,1H3\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1cccc(NNC(=O)c2cccnc2Cl)c1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(4-fluorobenzoyl)-n-(4-fluorophenyl)piperidine-1-carbothioamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H25F3N4O5/c1-16(2)22(23(35)26(27,28)29)32-21(34)14-33-20(17-8-4-3-5-9-17)12-11-19(24(33)36)31-25(37)38-15-18-10-6-7-13-30-18/h3-13,16,22H,14-15H2,1-2H3,(H,31,37)(H,32,34)\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][O][C][N][C][C][C][=C][C][=C][Branch1][=N][C][N][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" -0.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1ccccn1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CCOC(C)(c1ccccc1)c2ccccn2\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(\\\\C=C\\\\2/SC(=S)NC2=O)cc1OC\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-[4-[(4-chlorophenyl)-phenylmethyl]piperazin-1-yl]ethoxy]ethanol\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H17F2NO2/c20-16-5-1-13(2-6-16)18(23)14-9-11-22(12-10-14)19(24)15-3-7-17(21)8-4-15/h1-8,14H,9-12H2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][=C][Branch1][C][C][N][Ring1][O][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-1,3-thiazole-5-carboxamide\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H15Cl3N2O/c19-14-3-1-13(2-4-14)11-24-18(10-23-8-7-22-12-23)16-6-5-15(20)9-17(16)21/h1-9,12,18H,10-11H2\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=N][C][=Branch1][Ring2][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch1][N][C][=C][C][=N][C][Branch1][C][Cl][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1(C)CC(=O)c2c(N)c3ccccc3nc2C1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H32N2O3S/c1-2-15-27(25,26)23-12-6-9-20(17-23)21(24)22-13-10-19(11-14-22)16-18-7-4-3-5-8-18/h3-5,7-8,19-20H,2,6,9-17H2,1H3\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][=N][C][=Branch1][C][=O][N][C][C][N][Branch1][C][C][C][C][Branch1][C][F][=C][Ring1][#C][=N][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-piperidin-4-ylbenzamide\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" climb\\n\",\n        \"output\": \" climb is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H17NOS/c18-16(15-9-5-2-6-10-15)17-11-12-19-13-14-7-3-1-4-8-14/h1-10H,11-13H2,(H,17,18)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-methoxy-n,n'-bis(pyridin-3-ylmethyl)benzene-1,3-dicarboxamide\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cccc2sc(NC(=O)c3ccccc3)nc12\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H21ClN6O2/c1-14-2-3-16(13-17(14)26-18-5-7-24-21(22)27-18)25-20(29)15-4-6-23-19(12-15)28-8-10-30-11-9-28/h2-7,12-13H,8-11H2,1H3,(H,25,29)(H,24,26,27)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H20N2O4S/c1-13-7-8-18-17(11-13)21(14(2)24(18)12-20(25)26)15-9-10-23-22-16(15)5-4-6-19(22)29(3,27)28/h4-11H,12H2,1-3H3,(H,25,26)\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" fibre\\n\",\n        \"output\": \" fibre is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(4-methoxyphenyl)methyl]-2-([1,3]thiazolo[5,4-b]pyridin-2-ylsulfanyl)acetamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)CN1C(=O)NC(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CCC4\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][Branch1][Branch2][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27N5O2/c1-4-24-22(29)17-6-5-16(2)21(13-17)28-15-25-20-8-7-18(14-19(20)23(28)30)27-11-9-26(3)10-12-27/h5-8,13-15H,4,9-12H2,1-3H3,(H,24,29)\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][#Branch2][C][O][C][Branch1][=Branch2][C][N][C][=C][N][=C][Ring1][Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CCCN2c3ccccc3Sc4ccc(Cl)cc24)CC1\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H40N8O4/c33-15-11-31(12-16-34)23-26-20-19(21(27-23)29-7-3-1-4-8-29)25-24(32(13-17-35)14-18-36)28-22(20)30-9-5-2-6-10-30/h33-36H,1-18H2\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16)\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H21F3N2O4S/c1-12(15(22)20-8-11-21-9-2-3-10-21)13-4-6-14(7-5-13)25-26(23,24)16(17,18)19/h4-7,12H,2-3,8-11H2,1H3,(H,20,22)/t12-/m1/s1\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(7-hydroxy-4-methyl-2-oxochromen-3-yl)propanoic acid\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CC(C)(C)COc1nccc(Nc2cc(NC(=O)c3ccnc(c3)N4CCOCC4)ccc2C)n1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-[(3s)-piperidin-3-yl]oxybenzamide\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nc2ccc(OC(F)(F)F)cc2s1\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H5N3O2/c11-10(12)6-1-2-7-5(3-6)4-8-9-7/h1-4H,(H,8,9)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19)\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3cc(Cl)ccc3n1CC(=O)O\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch1][Ring2][=C][Ring1][P][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H15NO/c1-13-7-5-10(6-8-13)11-3-2-4-12(14)9-11/h2-5,9,14H,6-8H2,1H3\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=N][C][=C][N][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1-adamantyl)-2-[3-[(2r)-2-[[(2r)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl]amino]propyl]phenyl]acetamide\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[[5-bromo-4-(phenylamino)pyrimidin-2-yl]amino]benzoic acid\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C@H1][Ring1][Branch1][C][=Branch1][C][=O][N][C@@H1][Branch2][Ring1][Ring2][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C]\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-(2,6-dibromophenyl)pyrido[6,5-d]pyrimidine-2,7-diamine\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[[(5s)-3-(3-fluoro-4-imidazol-1-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-methyl-3-[[4-(pyridin-2-ylmethoxy)benzoyl]amino]phenyl]-3-morpholin-4-ylbenzamide\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H14N2/c1-11-7-8-14-13(9-11)15-10-12-5-3-2-4-6-12/h2-9H,10H2,1H3,(H,14,15)\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H23NO3/c1-4-9-18-14-7-5-6-8-15(14)19-11-13(17)10-16-12(2)3/h4-8,12-13,16-17H,1,9-11H2,2-3H3\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H30FN7O/c1-16(2)32-17(3)26-15-21(32)22-20(25)14-27-24(29-22)28-19-8-6-18(7-9-19)23(33)31-11-5-10-30(4)12-13-31/h6-9,14-16H,5,10-13H2,1-4H3,(H,27,28,29)\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-2-[[6-(phenylmethylamino)-9-propan-2-ylpurin-2-yl]amino]butan-1-ol\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[4-[[4-[(2-chloro-5-methylphenyl)amino]pyrimidin-2-yl]amino]phenoxy]-3-dimethylaminopropan-2-ol\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C@@H1][Branch1][C][C][C][N][Ring1][#C][C][=Branch1][C][=O][C][=C][C][C][=Branch1][=C][=C][N][Branch1][C][C][C][=Ring1][=Branch1][C][=C][Ring1][#Branch2][Cl][C][=Branch1][C][=O][C][=Branch1][C][=O][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-[(1r)-2-[3-[2-[2-(3-chlorophenyl)ethylamino]ethylsulfanyl]propylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H12I3NO4/c16-9-6-8(1-2-13(9)20)23-14-10(17)3-7(4-11(14)18)5-12(19)15(21)22/h1-4,6,12,20H,5,19H2,(H,21,22)\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-methoxyphenyl)prop-2-enamide\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][S][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COCCOc1ccc(cc1)C(=O)Nc2cc(NC(=O)c3cccc(c3)N(C)C)ccc2C\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H30ClN3O/c23-20-2-1-18(26-5-3-24-4-6-26)10-19(20)21(27)25-14-22-11-15-7-16(12-22)9-17(8-15)13-22/h1-2,10,15-17,24H,3-9,11-14H2,(H,25,27)\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccccc34)c2C(=O)N5C[C@H](O)CO5\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H28FN7O/c1-14(2)30-15(3)26-13-20(30)19-8-9-25-22(28-19)27-16-6-7-17(18(23)12-16)21(31)24-10-11-29(4)5/h6-9,12-14H,10-11H2,1-5H3,(H,24,31)(H,25,27,28)\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" pear\\n\",\n        \"output\": \" pear is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H26Cl2N2O/c1-3-27(4-2)23(28)18-7-5-16(6-8-18)22(17-11-13-26-14-12-17)19-9-10-20(24)21(25)15-19/h5-10,15,26H,3-4,11-14H2,1-2H3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][S][=Ring1][N]\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H21ClFN5O2/c1-30-18-9-16-13(8-12(18)10-28-7-3-6-17(28)20(24)29)21(26-11-25-16)27-15-5-2-4-14(22)19(15)23/h2,4-5,8-9,11,17H,3,6-7,10H2,1H3,(H2,24,29)(H,25,26,27)/t17-/m0/s1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][Branch1][Branch2][C][C][O][C][C][Ring1][=Branch1][C][=C][C][Branch1][C][F][=C][C][Branch2][Ring1][#Branch1][O][C][C][=C][C][=C][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][Ring1][Branch2][=C][Ring1][N][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H17NO3/c21-17-13-18(20-9-11-22-12-10-20)23-19-15(7-4-8-16(17)19)14-5-2-1-3-6-14/h1-8,13H,9-12H2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)Nc1sc(cc1C(=O)N[C@H]2CCCNC2)c3ccccc3\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-chloro-n-[2-(2-hydroxyethyl-phenylamino)-2-oxoethyl]-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H13NO3/c18-16(19)15-9-12-8-13(6-7-14(12)17-15)20-10-11-4-2-1-3-5-11/h1-9,17H,10H2,(H,18,19)\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][Branch1][=C][N][C][C@@H1][C][C][C][N][C@@H1][Ring1][=Branch1][C][Ring1][=Branch2][C][Branch1][C][F][=C][C][C][=Branch1][C][=O][C][=Branch1][S][=C][N][Branch1][=Branch1][C][C][C][Ring1][Ring1][C][Ring2][Ring1][Branch2][=Ring1][#Branch2][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H13ClFNO3/c1-10-17(23-13-5-2-11(18)3-6-13)14-8-12(19)4-7-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccccc1S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][NH1][C][=C][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H](CO)Nc1nc(SCc2cccc(Cl)c2F)nc3NC(=O)Sc13\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(N2CCN(CC2)C(=O)COCc3ccncc3)c(Cl)c1\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H23F3N4O5S/c1-14(2)19(20(33)24(25,26)27)30-18(32)12-31-21(17-9-6-10-37-17)28-11-16(22(31)34)29-23(35)36-13-15-7-4-3-5-8-15/h3-11,14,19H,12-13H2,1-2H3,(H,29,35)(H,30,32)\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H18F3N3O2/c1-15-7-9-20(30-23(32)17-4-2-6-19(13-17)25(26,27)28)14-22(15)31-24(33)18-8-10-21-16(12-18)5-3-11-29-21/h2-14H,1H3,(H,30,32)(H,31,33)\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H13NO2/c1-19-12-8-6-11(7-9-12)15-10-16(18)13-4-2-3-5-14(13)17-15/h2-10H,1H3,(H,17,18)\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidin-1-yl]sulfonylbenzamide\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][Branch1][N][N][C][C][=C][Branch1][C][C][NH1][N][=Ring1][=Branch1][=N][C][Branch2][Ring1][=Branch1][S][C][=C][C][=C][Branch1][O][N][C][=Branch1][C][=O][C][C][C][Ring1][Ring1][C][=C][Ring1][N][=N][Ring2][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H21N5O5/c1-26-6-7-28-17-21-15(19)14-16(22-17)23(18(25)20-14)10-12-5-3-4-11(8-12)9-13(24)27-2/h3-5,8H,6-7,9-10H2,1-2H3,(H,20,25)(H2,19,21,22)\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" buffet\\n\",\n        \"output\": \" buffet is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-n,n-dimethyl-2-[4-[[1-(pyridin-2-ylmethyl)indazol-5-yl]amino]quinazolin-5-yl]oxypropanamide\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(4-ethoxyphenyl)-2-ethylquinazolin-4-one\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[(4-chlorophenyl)sulfanylmethyl]-2-methyl-6-morpholin-4-ylpyrimidine\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(1-methylpyrrolidin-2-yl)pyridine\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-amino-4-(phenylamino)thieno[5,4-b]pyridine-2-carboxamide\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[(7r)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7h-pteridin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2,2-bis(difluoromethyl)-6-nitro-4-(1-oxidopyridin-1-ium-2-yl)-3h-1,4-benzoxazine\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H18F3N3O3/c1-10-7-13(16-22-17(27-24-16)18(19,20)21)8-11(2)15(10)25-6-4-5-14-9-12(3)23-26-14/h7-9H,4-6H2,1-3H3\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H19N5O4S/c18-14-11-15(21-17(20-14)27-7-9-4-2-1-3-5-9)22(8-19-11)16-13(25)12(24)10(6-23)26-16/h1-5,8,10,12-13,16,23-25H,6-7H2,(H2,18,20,21)/t10-,12-,13-,16-/m1/s1\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(4-tert-butylphenyl)-4-[4-[hydroxy-di(phenyl)methyl]piperidin-1-yl]butan-1-ol\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O]\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-chloro-n-(2-methyl-2,3-dihydroindol-1-yl)-3-sulfamoylbenzamide\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18ClN3O3S/c20-16-10-12-9-13(22-18(12)27-16)17(25)21-14-8-11-4-1-2-5-15(11)23(19(14)26)6-3-7-24/h1-2,4-5,9-10,14,22,24H,3,6-8H2,(H,21,25)\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(F)c(Nc2ccnc(Nc3ccc(cc3)S(=O)(=O)N)n2)c1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(8s)-1-azabicyclo[2.2.2]octan-8-yl]-5-phenylthiophene-2-carboxamide\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][=C][C][=C][Branch1][=Branch2][C][=C][Ring1][=Branch1][C][Ring1][=Branch2][=O][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][C@H1][Ring1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H24ClN5O2/c1-27(2)13-17(28)14-29-18-10-8-16(9-11-18)25-21-23-12-19(22)20(26-21)24-15-6-4-3-5-7-15/h3-12,17,28H,13-14H2,1-2H3,(H2,23,24,25,26)\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC1CCc2cc(OC(=O)c3ccccc3)c(OC(=O)c4ccccc4)cc2C1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H18N2/c1-2-5-8-6-3-4-7-9(10)11-8/h8H,2-7H2,1H3,(H2,10,11)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1N2CCS(=O)(=O)C2=Nc3ccccc13\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H28N2O5/c1-2-31-24(30)20(14-12-17-8-4-3-5-9-17)25-19-15-13-18-10-6-7-11-21(18)26(23(19)29)16-22(27)28/h3-11,19-20,25H,2,12-16H2,1H3,(H,27,28)\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (5r)-3-[4-(1,1-dioxo-3,6-dihydro-2h-thiopyran-4-yl)-3-fluorophenyl]-5-[(5-fluorotriazol-1-yl)methyl]-1,3-oxazolidin-2-one\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" N(c1ccccc1)c2ccnc(Nc3ccccc3)n2\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-hydroxy-2-methyl-3-phenylchromen-4-one\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2ccnc(Nc3ccc(cc3)C(=O)N)n2\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C28H26F3N3O6/c1-16(2)24(25(37)28(29,30)31)33-23(36)15-34-21(17-8-4-3-5-9-17)13-12-20(26(34)38)32-22(35)14-18-10-6-7-11-19(18)27(39)40/h3-13,16,24H,14-15H2,1-2H3,(H,32,35)(H,33,36)(H,39,40)\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C31H37N5O3/c1-22-9-11-23(12-10-22)36-29(21-28(34-36)31(2,3)4)33-30(37)32-26-13-14-27(25-8-6-5-7-24(25)26)39-20-17-35-15-18-38-19-16-35/h5-14,21H,15-20H2,1-4H3,(H2,32,33,37)\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" dessert\\n\",\n        \"output\": \" dessert is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=N][O][C][=C][C][Branch2][Ring1][=Branch2][O][C][C][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][C][N][=N][Ring1][#Branch1][=C][C][=C][Ring2][Ring1][=Branch2][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" bagpipe\\n\",\n        \"output\": \" bagpipe is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch1][#Branch2][C][C][O][C][C][C][C][Ring1][Ring1][C][=C][Ring1][=N]\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H21Cl2NO5/c1-31-19-7-4-8-20(32-2)21(19)15-11-9-14(10-12-15)13-18(24(29)30)27-23(28)22-16(25)5-3-6-17(22)26/h3-12,18H,13H2,1-2H3,(H,27,28)(H,29,30)/t18-/m0/s1\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][Cl][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H23NO3/c1-16(13-22(24)25)9-10-17-5-4-7-20(14-17)26-15-19-12-11-18-6-2-3-8-21(18)23-19/h2-8,11-12,14,16H,9-10,13,15H2,1H3,(H,24,25)\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H10FNO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m0/s1\\n\",\n        \"output\": \" -1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][=Branch1][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H27N7O3S/c1-4-29(13-12-28(2)3)33(31,32)18-9-7-16(8-10-18)19-15-25-21(23)20(27-19)22(30)26-17-6-5-11-24-14-17/h5-11,14-15H,4,12-13H2,1-3H3,(H2,23,25)(H,26,30)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(CCOc1ccc(NS(=O)(=O)C)cc1)CCc2ccc(NS(=O)(=O)C)cc2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H13Cl2F3N4O2/c21-15-5-4-12(28-18(30)10-2-1-3-11(6-10)20(23,24)25)7-14(15)19(31)29-13-8-16(22)17(26)27-9-13/h1-9H,(H2,26,27)(H,28,30)(H,29,31)\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][=C][C][Branch2][Ring1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][C][=C][Ring2][Ring1][Ring1][Cl][C][=C][Ring2][Ring1][=N][Cl]\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H28F3N3O2/c1-16-11-24(31-23-14-20(32-2)9-10-22(16)23)30-19-7-4-6-18(13-19)29-15-17-5-3-8-21(12-17)33-25(26,27)28/h3,5,8-12,14,18-19,29H,4,6-7,13,15H2,1-2H3,(H,30,31)/t18-,19-/m0/s1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1OCCN4CCN(C)CC4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CCNC(=O)c1c(C)[nH]c(\\\\C=C\\\\2/C(=O)Nc3ccc(F)cc23)c1C\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[2-[[2-hydroxy-3-(phenoxy)propyl]amino]ethoxy]phenoxy]acetamide\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-phenylquinoline-4-carboxylic acid\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3ccccn3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(NCCCN1CCCCC1)C(c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-chloro-2-[[4-(phenylmethylsulfonyl)piperazin-1-yl]methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](NC(=O)c1c(O)c(nc2ccccc12)c3ccccc3)c4ccccc4\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(6,7,8,9,10,11-hexahydrocycloocta[b]indol-5-yl)-n,n-dimethylpropan-1-amine\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCN(CCCC)CCCOC(=O)c1ccc(N)cc1\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C(Oc1ccccc1)C2CNCCO2\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[(4-bromo-2,6-difluorophenyl)methoxy]-5-(4-pyrrolidin-1-ylbutylcarbamoylamino)-1,2-thiazole-4-carboxamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H5Cl3N2O2/c11-10(12,13)8-5-4-6-2-1-3-7(15(16)17)9(6)14-8/h1-5H\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H13Cl2N3O4S/c19-14-15-12(28-16(14)20)6-9(21-15)17(26)22-10-5-8-3-1-2-4-11(8)23(18(10)27)7-13(24)25/h1-4,6,10,21H,5,7H2,(H,22,26)(H,24,25)\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H27ClN2O3/c29-22-5-7-24-21(4-6-23(31-24)19-2-1-3-20(11-19)27(33)34)25(22)26(32)30-15-28-12-16-8-17(13-28)10-18(9-16)14-28/h1-7,11,16-18H,8-10,12-15H2,(H,30,32)(H,33,34)\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CCOc1ccccc1Cc2ccccc2\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][Branch2][Ring1][Branch2][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring1][#C][=Ring1][O]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2nsnc2c1NC3=NCCN3\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(2-methyl-5-nitroimidazol-1-yl)ethanol\\n\",\n        \"output\": \" -0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)CCC(=O)c1ccc(cc1)c2ccccc2\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][S][S+1][Branch1][C][O-1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][S][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(propan-2-ylamino)-3-[4-(2-propan-2-yloxyethoxymethyl)phenoxy]propan-2-ol\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H23N3O/c1-2-20(17-11-5-3-6-12-17)28-25(29)22-19-15-9-10-16-21(19)27-24(23(22)26)18-13-7-4-8-14-18/h3-16,20H,2,26H2,1H3,(H,28,29)/t20-/m0/s1\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][N][C][C@H1][Branch1][C][O][C][O][C][=N][S][N][=C][Ring1][Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCNC(=O)NS(=O)(=O)c1ccc(C)cc1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@]12CC[C@H]3[C@@H](CCc4cc(O)ccc34)[C@@H]1CCC2=O\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-ethyl-4-[[4-[2-(2h-tetrazol-5-yl)phenyl]phenyl]methoxy]-5,6,7,8-tetrahydroquinoline\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][S][C][C][C][N][Branch2][Ring2][Ring2][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][Branch1][C][C][C][C][C][C][Branch1][Ring2][C][Ring1][Branch1][C][Ring1][Branch2][Branch1][C][C][C]\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" receipt\\n\",\n        \"output\": \" receipt is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(F)c(F)c4\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)N(CCC(C(=O)N)(c1ccccc1)c2ccccn2)C(C)C\\n\",\n        \"output\": \" -0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][O][Ring1][#C]\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H14O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-10H,11-12H2\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3ccc(Cl)cc3n1CC(=O)O\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(4-chlorophenyl)-phenylmethyl]-4-[(3-methylphenyl)methyl]piperazine\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1CCN(CC1)C(=O)CN2C(=O)C(Cc3ccccc23)NC(=O)c4cc5cc(Cl)sc5[nH]4\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H10N2O2S/c14-11(12-7-3-4-7)8-6-9(15-13-8)10-2-1-5-16-10/h1-2,5-7H,3-4H2,(H,12,14)\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(propan-2-ylamino)-3-(2-prop-2-enylphenoxy)propan-2-ol\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H15NO5/c1-25-17(22)9-8-16(21)20-11-6-7-14-15(10-11)12-4-2-3-5-13(12)18(23)19(14)24/h2-7,10H,8-9H2,1H3,(H,20,21)\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc(cc1)c2nc3ccc(O)cc3s2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)CCN1S(=O)(=O)c3ccccc3\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC1=NC(Nc2c(F)ccc(F)c12)c3occc3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H16ClN5OS2/c1-8(6-22)18-12-11-13(19-14(17)24-11)21-15(20-12)23-7-9-3-2-4-10(16)5-9/h2-5,8,22H,6-7H2,1H3,(H3,17,18,19,20,21)/t8-/m1/s1\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C32H37N3O5S/c1-6-22(7-2)19-33-31(36)24-14-15-28-27(17-24)26(20-35(28)4)16-23-12-13-25(18-29(23)40-5)32(37)34-41(38,39)30-11-9-8-10-21(30)3/h8-15,17-18,20,22H,6-7,16,19H2,1-5H3,(H,33,36)(H,34,37)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H8O4/c1-6(12)9-4-7-2-3-8(13)5-10(7)15-11(9)14/h2-5,13H,1H3\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][Ring1][#C][=O]\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OS(=N)(=O)Cc1noc2ccccc12\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1cc2ccccc2n1Cc3ccccc3\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H18ClFN2O4/c1-25-5-6-27-19-10-15-11(7-18(19)26-2)14(3-4-22-15)23-16-9-17(24)12(20)8-13(16)21/h3-4,7-10,24H,5-6H2,1-2H3,(H,22,23)\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]oxypiperidin-1-yl]acetamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H17N3O3S/c1-26-17-10-8-16(9-11-17)23-14-21-19-13-15(7-12-20(19)23)22-27(24,25)18-5-3-2-4-6-18/h2-14,22H,1H3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-3-cyclopentyl-2-(4-methylsulfonylphenyl)-n-(1,3-thiazol-2-yl)propanamide\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H15NO/c1-12(13-7-3-2-4-8-13)17-11-14-9-5-6-10-15(14)16(17)18/h2-10,12H,11H2,1H3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch1][C][N][C][O][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][O]\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C1Oc2ccccc2C3=NN(CC13)c4ccccc4\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[2-oxo-2-[[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]amino]ethyl]benzoic acid\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H15ClN4O4S/c19-14-7-10-6-11(21-17(10)28-14)16(25)20-12-5-9-3-1-2-4-13(9)23(18(12)26)8-15(24)22-27/h1-4,6-7,12,21,27H,5,8H2,(H,20,25)(H,22,24)\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H9F3N8/c14-13(15,16)12-20-19-11-6-5-10(21-24(11)12)17-7-23-9-4-2-1-3-8(9)18-22-23/h1-6H,7H2,(H,17,21)\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Ring2][C][Branch1][=Branch2][C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-methoxy-n,2,6-trimethyl-n-[2-[2-[4-(1-methylpiperidin-4-yl)piperidin-1-yl]-2-oxoethoxy]ethyl]benzenesulfonamide\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H10N2O2/c15-7-1-3-9-10-4-2-8(16)6-12(10)14(18)13(17)11(9)5-7/h1-6H,15-16H2\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" numeric\\n\",\n        \"output\": \" numeric is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H19F2N3O3/c1-3-21-8-11(17(24)25)16(23)10-6-12(18)15(13(19)14(10)21)22-5-4-20-9(2)7-22/h6,8-9,20H,3-5,7H2,1-2H3,(H,24,25)\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H13N3/c1-11-5-4-6-12(9-11)18-15-13-7-2-3-8-14(13)16-10-17-15/h2-10H,1H3,(H,16,17,18)\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" apartment\\n\",\n        \"output\": \" apartment is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-ethoxy-4-[2-[[(1s)-3-methyl-1-(2-piperidin-1-ylphenyl)butyl]amino]-2-oxoethyl]benzoic acid\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H24O2/c1-12-10-14-15-4-5-18(22)20(15,3)9-7-16(14)19(2)8-6-13(21)11-17(12)19/h6,8,11,14-16H,1,4-5,7,9-10H2,2-3H3/t14-,15-,16-,19+,20-/m0/s1\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1OC)C(=O)Nc2cc(NC(=O)c3cccc(c3)N(C)C)ccc2C\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H18ClN3O/c1-21-8-10-22(11-9-21)18-14-12-13(19)6-7-16(14)23-17-5-3-2-4-15(17)20-18/h2-7,12H,8-11H2,1H3\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H15NO/c15-11-14(16,12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,16H,11,15H2\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1CCN(CC1)C(=O)c2scc3OCCOc23\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccc2c(c1)C(=O)C(=O)c3cc(N)ccc23\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C33H30N4O2/c1-4-9-30-35-31-21(2)18-24(32-34-27-12-7-8-13-28(27)36(32)3)19-29(31)37(30)20-22-14-16-23(17-15-22)25-10-5-6-11-26(25)33(38)39/h5-8,10-19H,4,9,20H2,1-3H3,(H,38,39)\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-methylbenzene-1,2-diol\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(CN2CC3CNCC(C2)O3)cc1C(=O)NCC45CC6CC(CC(C6)C4)C5\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-phenylquinoline\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C(Nc1ncnc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring1][=C][NH1][Ring1][P]\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2-dimethylamino-2-phenylbutyl) 3,4,5-trimethoxybenzoate\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-2-[[2-amino-5-[(2,3-difluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]propan-1-ol\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cccs2)NC(=O)OCC(F)(F)F)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OCC(O)COC(=O)c1ccccc1Nc2ccnc3cc(Cl)ccc23\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=C(C(=O)N(C[C@H](N)c2ccccc2)C(=O)N1Cc3c(F)cccc3F)c4ccccc4F\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H23N3O6/c1-29-16-10-8-14(12-18(16)31-3)22(27)25-20-6-5-7-21(24-20)26-23(28)15-9-11-17(30-2)19(13-15)32-4/h5-13H,1-4H3,(H2,24,25,26,27,28)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)OCc3ccccn3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,5-dimethyl-2-phenylpyrazol-3-one\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)N1CCN(CC1)c2ccc(NC(=O)c3oc(Nc4ccccc4F)nn3)cc2\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][Branch1][C][C][C][=N][C][Branch2][Ring1][Branch1][C][N][C][=N][C][=C][Branch1][C][Cl][N][=C][Branch1][C][N][N][=C][Ring1][O][Ring1][Branch2][=C][Ring2][Ring1][Ring1][C]\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-dimethylamino-n-(9-ethylcarbazol-3-yl)acetamide\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][N][C][=Branch1][C][=O][C][Branch2][Ring1][Branch1][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][S][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][=N][C][N][C][C@@H1][C][C@H1][Ring1][Branch1][C][N][Ring1][Branch1][C][=C][Ring1][=C][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-methyl-n-phenylthiadiazole-5-carboxamide\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H23FN2O4S2/c21-18-12-22-20(28-18)23-19(24)17(11-13-7-9-27-10-8-13)14-1-3-15(4-2-14)29(25,26)16-5-6-16/h1-4,12-13,16-17H,5-11H2,(H,22,23,24)/t17-/m1/s1\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" sideboard\\n\",\n        \"output\": \" sideboard is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H18ClN3O3/c20-14-6-7-16-13(10-14)11-17(22-16)19(26)21-12-18(25)23(8-9-24)15-4-2-1-3-5-15/h1-7,10-11,22,24H,8-9,12H2,(H,21,26)\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(4-phenylpiperazin-1-yl)-2-phenylsulfanylethanone\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccccc1Nc2oc(nn2)C(=O)Nc3ccc(cc3)N4CCOCC4\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H24N4O2/c1-15-3-5-17(6-4-15)14-25-19(24)23-11-7-16(8-12-23)13-22-18-20-9-2-10-21-18/h2-6,9-10,16H,7-8,11-14H2,1H3,(H,20,21,22)\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H28O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-15,18,22,26H,3-8,10-11H2,1-2H3/t14-,15-,18+,19-,20-,21-/m0/s1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H25NO6/c1-24-20(23)15-27-19-9-7-18(8-10-19)25-12-11-21-13-16(22)14-26-17-5-3-2-4-6-17/h2-10,16,21-22H,11-15H2,1H3\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (3r)-n-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(CC(=O)c2ccc(O)cc2O)cc1\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1cc(O)c2C(=O)C(=COc2c1)c3ccc(O)c(O)c3\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (8s,9s,10r,13s,14s,17s)-17-acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21F2N7O2/c20-15(21)16-22-13-3-1-2-4-14(13)28(16)19-24-17(26-5-9-29-10-6-26)23-18(25-19)27-7-11-30-12-8-27/h1-4,15H,5-12H2\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CC(=O)N2c3ccccc3C(=O)Nc4cccnc24)CC1\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)S(=O)(=O)c2ccc(c3cnc(N)c(n3)C(=O)Nc4cccnc4)c(c2)C(F)(F)F\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2c(Nc3ncc(CC(=O)Nc4cccc(F)c4)s3)ncnc2cc1OCCCN5CCC(CO)CC5\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl (2s)-2-(2-chlorophenyl)-2-(6,7-dihydro-4h-thieno[3,2-c]pyridin-5-yl)acetate\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-(propan-2-ylamino)propan-2-ol\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=N][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][C][C][C][N][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][C][C][C][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-chloro-2-hydroxy-n-phenylbenzamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-hydroxy-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" FC(F)(F)c1cc(CO[C@H]2CCCN[C@H]2c3ccccc3)cc(c1)C(F)(F)F\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5,7-dihydroxy-2-phenylchromen-4-one\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-chloro-3-(dichloromethyl)-1,1-dioxo-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][Branch1][C][C][NH1][C][C][C][C][Branch1][#Branch2][C][N][C][C][O][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring2][Ring1][C][=Ring1][=C]\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[1-(benzoyl)-2-methyl-3,4-dihydro-2h-quinolin-4-yl]acetamide\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(2-amino-6-oxo-3h-purin-9-yl)methoxy]ethyl (2s)-2-amino-3-methylbutanoate\\n\",\n        \"output\": \" -1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(C1CCN(CC[C@@H](c2ccccc2)c3ccc(cc3)S(=O)(=O)C)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nc(N)nc(n1)c2cccc(c2)C(F)(F)F\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(NC(=O)N2CCN(C[C@@H]3CCCN(Cc4ccccc4)C3)CC2)cc1Cl\\n\",\n        \"output\": \" 4.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H26N2S2/c1-22-13-6-5-7-16(22)12-14-23-18-8-3-4-9-20(18)25-21-11-10-17(24-2)15-19(21)23/h3-4,8-11,15-16H,5-7,12-14H2,1-2H3\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-(4-methylphenoxy)phenoxy]-n-pyridin-4-ylacetamide\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC[C@H](Nc1ncc(Cl)c(Nc2cc([nH]n2)C3CC3)n1)c4ccc(F)cc4\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(9-methylsulfonylcarbazol-3-yl)morpholine-4-carboxamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(4-fluorophenyl)-6-methylsulfonyl-1-oxidopyridin-1-ium-3-carboxamide\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H16FNO6S2/c1-11-15(10-18(21)22)16-9-12(19)3-8-17(16)20(11)28(25,26)14-6-4-13(5-7-14)27(2,23)24/h3-9H,10H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" -0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H10N2OS/c1-12-11-13-7-9(15-11)10(14)8-5-3-2-4-6-8/h2-7H,1H3,(H,12,13)\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H22N2/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21/h2-3,6-12H,4-5,13-15H2,1H3/b18-11+\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]-n-(2-methoxyethyl)benzamide\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch2][Ring1][C][C][=Branch1][C][=O][O][C][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H21N3O/c1-4-21-16-8-6-5-7-14(16)15-11-13(9-10-17(15)21)19-18(22)12-20(2)3/h5-11H,4,12H2,1-3H3,(H,19,22)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H17N3O/c1-12(2)18(22)21-17-14-8-4-3-7-13(14)11-16(20-17)15-9-5-6-10-19-15/h3-12H,1-2H3,(H,20,21,22)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][N][Branch1][S][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1][Ring1][S]\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C34H39Cl2N3O5/c1-42-28-19-23(20-29(43-2)30(28)44-3)31(40)39-18-12-33(22-39,25-9-10-26(35)27(36)21-25)11-15-38-16-13-34(14-17-38,32(37)41)24-7-5-4-6-8-24/h4-10,19-21H,11-18,22H2,1-3H3,(H2,37,41)/t33-/m0/s1\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" [O-][N+](=O)c1cccc(c1)C(=O)Nc2nc3ccccc3n2CCN4CCOCC4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H22ClN3O3/c1-25(2)21(28)19(26)17(10-13-6-4-3-5-7-13)24-20(27)18-12-14-11-15(22)8-9-16(14)23-18/h3-9,11-12,17,19,23,26H,10H2,1-2H3,(H,24,27)/t17-,19+/m0/s1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O[C@@H](CNCCc1ccc(CNCCc2ccccn2)cc1)c3ccc(O)c4NC(=O)Sc34\\n\",\n        \"output\": \" -0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H17N3O2/c1-21-15-8-13-14(9-16(15)22-2)19-11-20-17(13)18-10-12-6-4-3-5-7-12/h3-9,11H,10H2,1-2H3,(H,18,19,20)\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][Branch1][=C][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][=N][C][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][N][=C][Branch1][Branch2][S][C][Ring1][=Branch1][=N][Ring1][O][C][=Branch1][C][=O][N][C][C][C][Ring1][Ring1]\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(5-dimethylaminonaphthalen-1-yl)sulfonyl-methylamino]acetic acid\\n\",\n        \"output\": \" -1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(=O)Nc1nc(cc2ccccc12)c3ccccn3\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1cc(ccc1NC(=O)Nc2ccccc2Br)[N+](=O)[O-]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1nc(cs1)c2cccs2\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][=N][C][=C][Branch2][Ring1][C][\\\\C][=C][Branch1][=Branch2][/C][C][=C][C][=C][S][Ring1][Branch1][\\\\C][=Branch1][C][=O][O][N][Ring1][S][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C1Oc2ccc(Oc3cc(Oc4ccc(cc4)n5ccnc5)ncn3)cc2O1\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][Branch1][Branch1][C][C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring1][Ring1][C][C][=N][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][C][N][C][=Branch1][C][=O][C][C][C][Ring1][=Branch1][=O]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=C][C][=C][Branch1][C][Br][C][=C][C][Ring1][#Branch1][=N][Ring1][N]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc2OCOc2c1Nc3ncnc4cc(OCCCN5CCCC5)cc(OC6CCOCC6)c34\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n,n-di(propan-2-yl)-1,3,4-thiadiazole-2,5-diamine\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][Branch2][Ring1][Branch1][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][Ring2][C][C][Cl][C][C][Cl][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H21N/c1-10-3-9-4-11(2,6-10)8-12(13,5-9)7-10/h9H,3-8,13H2,1-2H3\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-2-[2-[(1r)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1CCC[C@H]1CNC(=O)c2c(OC)ccc(Br)c2OC\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[4-methyl-5-[(z)-(2-oxo-1h-indol-3-ylidene)methyl]-1h-pyrrol-3-yl]propanoic acid\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][Branch1][Ring1][C][C][C][O][C][=Branch1][C][=O][C][C][Branch1][S][C][=Branch1][C][=O][O][C][C][Branch1][Ring1][C][C][C][C][C][C][S][=Branch1][C][=O][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(3-methylphenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" popcorn\\n\",\n        \"output\": \" popcorn is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-acetamido-n-(2-aminophenyl)benzamide\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H32ClN5O2/c1-15(2)26-13-19(17-4-6-18(25)7-5-17)24(32)30-10-8-29(9-11-30)23-21-16(3)12-20(31)22(21)27-14-28-23/h4-7,14-16,19-20,26,31H,8-13H2,1-3H3/t16-,19-,20-/m1/s1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCS(=O)(=O)c1ccc(c(C)c1)c2cc(Cl)ccc2OCC(=O)O\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc(Nc2ccc(cc2)S(=O)(=O)N)nn1C(=O)c3c(F)cccc3F\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-phenylsulfonyl-2h-pyrazol-3-amine\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-ethylpyridine-4-carbothioamide\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-amino-n-(phenylmethyl)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3,5-dichloro-n-[[(2s)-1-ethylpyrrolidin-2-yl]methyl]-2-hydroxy-6-methoxybenzamide\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(Oc2ccc(OCC(=O)Nc3ccncc3)cc2)cc1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14N4O2S/c17-23(21,22)14-8-6-13(7-9-14)19-16-18-11-10-15(20-16)12-4-2-1-3-5-12/h1-11H,(H2,17,21,22)(H,18,19,20)\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H28N2O3/c1-16-7-11-19(24-22(27)14-8-17-5-3-2-4-6-17)15-21(16)25-23(28)18-9-12-20(26)13-10-18/h7,9-13,15,17,26H,2-6,8,14H2,1H3,(H,24,27)(H,25,28)\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (6s,8s,9s,10r,11s,13s,14s,17s)-17-acetyl-11-hydroxy-6,10,13-trimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[4-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]phenyl]-1,1-dimethylurea\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" c1ccc2[nH]ncc2c1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H12N4OS/c1-14(2)5-3-4-13-10-6(5)7(11)8(16-10)9(12)15/h3-4H,11H2,1-2H3,(H2,12,15)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCCC\\\\N=C\\\\1/C=CN(Cc2ccccc2)c3cc(Cl)ccc13\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][=N][C][C][C][Branch1][C][C][=N][NH1][C][=Ring1][=Branch1][C][=C][Ring1][=N][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-phenylquinolin-4-amine\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H17NO2S/c1-12-8-9-15-14(10-12)18(16(19(15)2)11-17(20)21)22-13-6-4-3-5-7-13/h3-10H,11H2,1-2H3,(H,20,21)\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[3-[[5-bromo-4-[3-(thiophene-2-carbonylamino)propylamino]pyrimidin-2-yl]amino]phenyl]pyrrolidine-1-carboxamide\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H30F3N3O/c1-15-19-14-29(7-6-28-8-10-30-11-9-28)5-4-16(19)12-21-22(15)18-13-17(23(24,25)26)2-3-20(18)27-21/h2-3,13,15-16,19,27H,4-12,14H2,1H3/t15-,16-,19-/m0/s1\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H25FN6O/c1-14(2)28-15(3)23-13-19(28)20-18(22)12-24-21(26-20)25-16-4-6-17(7-5-16)27-8-10-29-11-9-27/h4-7,12-14H,8-11H2,1-3H3,(H,24,25,26)\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][Branch1][C][N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][N][=C][C][=C][Ring1][=Branch1][C][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][O][C][Ring1][#Branch1][=C][Ring1][O][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H17ClN2O5S/c1-11-19(28(26,27)14-8-6-13(20)7-9-14)18-15(21-12(2)23)4-3-5-16(18)22(11)10-17(24)25/h3-9H,10H2,1-2H3,(H,21,23)(H,24,25)\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][Branch1][C][Cl][N][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][O][C][=Branch1][C][=O][N][C][=N][C][=Branch1][C][=O][N][Branch1][=Branch1][C][=C][Ring1][#Branch1][F][C@@H1][O][C@H1][Branch1][C][C][C@@H1][Branch1][C][O][C@H1][Ring1][#Branch1][O]\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H21ClN4O5S/c22-17-7-12-6-14(25-20(12)32-17)19(30)24-15-5-11-3-1-2-4-16(11)26(21(15)31)8-18(29)23-13(9-27)10-28/h1-4,6-7,13,15,25,27-28H,5,8-10H2,(H,23,29)(H,24,30)\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C@H1][Branch1][C][C][O][C][=C][C][Branch1][#C][O][C@@H1][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Ring2][=C][Ring1][S][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(NCC(O)c1ccc(cc1)[N+](=O)[O-])C23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][Branch1][C][I][C][=C][Branch1][C][I][C][=C][C][=C][N][=C][Ring1][N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-methylbenzamide\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2nc(Nc3ccc(C(=O)NC4CCN(C)CC4)c(F)c3)ncc2F\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=CC(=O)Nc2ccccc12\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][Branch1][#C][C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][=N][O][C][C][=C][N][=C][Branch1][C][Cl][S][Ring1][=Branch1][=C][Ring1][=C]\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-methyl-2-[3-(1-methylpiperidin-4-yl)-1h-indol-5-yl]ethanesulfonamide\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C32H39FN2O5S2/c1-4-35(32(36)23-24-5-13-29(14-6-24)41(2,37)38)28-17-20-34(21-18-28)22-19-31(25-7-11-27(33)12-8-25)26-9-15-30(16-10-26)42(3,39)40/h5-16,28,31H,4,17-23H2,1-3H3/t31-/m0/s1\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H](C1=CNC(=S)N1)c2cccc(C)c2C\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-piperidin-1-yl-3-(trifluoromethyl)-[1,2,4]triazolo[3,4-f]pyridazine\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (6s)-6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H16N6O2S/c1-27(25,26)13-5-2-4-12(10-13)21-18-19-9-8-17(23-18)22-15-6-3-7-16-14(15)11-20-24-16/h2-11H,1H3,(H,20,24)(H2,19,21,22,23)\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(C[C@@H](C)NC[C@H](O)c2ccc(O)c(NC=O)c2)cc1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][S][C][=Branch1][=Branch1][=N][C][Ring1][Branch1][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-methyl-5-(phenylmethylamino)-1,2,4-thiadiazol-3-one\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][S][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][N][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][Ring1][#C]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H16Cl2N4O3S/c1-7-10(16)11(17)12(19-7)13(22)20-8-2-4-21(5-3-8)15-18-6-9(25-15)14(23)24/h6,8,19H,2-5H2,1H3,(H,20,22)(H,23,24)\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H9N3O3S/c1-5(14)8-7(6(2)16-13-8)9(15)12-10-11-3-4-17-10/h3-4H,1-2H3,(H,11,12,15)\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-[2-[2-(4-methanesulfonamidophenyl)ethyl-methylamino]ethoxy]phenyl]methanesulfonamide\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H20N4O3/c22-18-5-1-2-6-19(18)25-20(26)17-9-7-15(8-10-17)13-24-21(27)28-14-16-4-3-11-23-12-16/h1-12H,13-14,22H2,(H,24,27)(H,25,26)\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-1-(2,6-dimethylphenoxy)propan-2-amine\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1nnc2CN=C(c3ccccc3Cl)c4cc(Cl)ccc4n12\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(2-methoxyphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)S(=O)(=O)Nc2nnc(s2)c3ccccc3\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][C][C][N][Branch1][#Branch1][C][C][Ring1][=Branch1][Ring1][Branch1][C][=N][C][N][Branch2][Ring1][=Branch1][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=Ring1][#Branch2][C][=C][Ring1][=C][F][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H24N4O3S/c20-17(24)15-12-16(27-18(15)22-19(21)25)13-4-6-14(7-5-13)26-11-10-23-8-2-1-3-9-23/h4-7,12H,1-3,8-11H2,(H2,20,24)(H3,21,22,25)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H20N2O/c1-4-20-16-8-6-5-7-14(16)15-11-13(9-10-17(15)20)19-18(21)12(2)3/h5-12H,4H2,1-3H3,(H,19,21)\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)c3cccc(NC(=O)C)c3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(SC2=NN3C=NC(=O)C(=C3C=C2)c4c(Cl)cccc4Cl)c(F)c1\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1oc(cc1C(=O)O)c2ccc(Cl)cc2\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C7H4ClFN2/c8-4-1-6-7(2-5(4)9)11-3-10-6/h1-3H,(H,10,11)\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H15N3O2/c1-20-14-8-12-13(9-15(14)21-2)17-10-18-16(12)19-11-6-4-3-5-7-11/h3-10H,1-2H3,(H,17,18,19)\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-2-[[(2s)-2-acetamido-4-methylpentanoyl]amino]-4-methyl-n-[(2s)-1-oxohexan-2-yl]pentanamide\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)C1=C(C)c2cnc(Nc3ccc(cn3)N4CCNCC4)nc2N(C5CCCC5)C1=O\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(phenylmethoxy)-1h-indole-2-carboxylic acid\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(7-hydroxy-4,8-dimethyl-2-oxochromen-3-yl)propanoic acid\\n\",\n        \"output\": \" -0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-methyl-6-phenyl-3-pyridin-4-yl-[1,2]oxazolo[4,5-c]pyridin-4-one\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H](N)C(=O)N[C@@H](CCc1ccccc1)\\\\C=C\\\\S(=O)(=O)c2ccccc2\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H12N2OS/c10-8(12)7-5-3-1-2-4-6(5)13-9(7)11/h1-4,11H2,(H2,10,12)\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][#C][N][C][=C][C][=C][Branch1][P][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][Branch1][C][F][=C][Ring1][P][=N][C][=C][Ring2][Ring1][Branch2][F]\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-tert-butyl-3-(4-methylphenyl)pyrazolo[4,5-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=N][C][C][C][Branch1][C][N][=N][NH1][C][=Ring1][=Branch1][N][C][=C][Ring1][=C]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][N][C][C][C][N][Branch2][Ring1][S][C][C][C@@H1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring2][Ring1][=Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch2][Ring1][Branch2][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H20N6O4S/c21-19-18(20(27)24-15-2-1-7-22-12-15)25-17(13-23-19)14-3-5-16(6-4-14)31(28,29)26-8-10-30-11-9-26/h1-7,12-13H,8-11H2,(H2,21,23)(H,24,27)\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16N2O3/c1-10-9-18-15(11(10)6-7-16(20)21)8-13-12-4-2-3-5-14(12)19-17(13)22/h2-5,8-9,18H,6-7H2,1H3,(H,19,22)(H,20,21)/b13-8-\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=C(C)C(=O)C(=C(C)C1=O)C(CCCCCC(=O)O)c2ccccc2\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[3-bromo-4-[(2,4-difluorophenyl)methoxy]-6-methyl-2-oxopyridin-1-yl]-n,4-dimethylbenzamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14N2O/c1-14(2,12-6-4-8-16-10-12)13(17)11-5-3-7-15-9-11/h3-10H,1-2H3\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" [O-][N+](=O)c1ccc2c(c1)nc3CCCCCn23\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(1,3-benzodioxol-5-ylmethyl)-1h-pyrazole-3,5-diamine\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H11ClN2O2/c16-10-4-1-3-9(7-10)8-18-14(19)11-5-2-6-12(17)13(11)15(18)20/h1-7H,8,17H2\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)c2cc3cc(F)ccc3[nH]2\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H14ClN5/c1-12-17(24-10-3-2-7-16(24)21-12)15-8-9-20-18(23-15)22-14-6-4-5-13(19)11-14/h2-11H,1H3,(H,20,22,23)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CS(=O)(=O)c1ccc(cc1)[C@@H](CC2CCCC2)C(=O)Nc3nccs3\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H27NO3/c1-2-14-22-15-18(23)16-25-21-11-7-6-10-19(21)20(24)13-12-17-8-4-3-5-9-17/h3-11,18,22-23H,2,12-16H2,1H3\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[1-(3,4-dihydro-1h-isoquinolin-2-yl)-1-oxopropan-2-yl]isoindole-1,3-dione\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=N][C][Branch2][Ring1][=C][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=N][C][=C][Ring2][Ring1][=Branch2][N][Branch1][C][C][C][Ring2][Ring2][Ring1][=O]\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H9F3N6/c13-12(14,15)11-19-18-10-4-3-9(20-21(10)11)17-7-8-2-1-5-16-6-8/h1-6H,7H2,(H,17,20)\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2c(Nc3c(Cl)ccc4OCOc34)ncnc2cc1OCCCN5CCCC5\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][S][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3cc(ccc3n1CC(=O)O)c4ccccc4\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCC[C@@H]1CCO[C@](C)(c2ccccc2)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][=N][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][C][Branch1][C][O][C][C][C][C][C][C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-ethoxychromen-2-one\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=N][NH1][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][#C][C][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][Ring1][Branch2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-chlorophenyl)-4-(phenylmethyl)pyrazolo[4,5-c]isoquinolin-4-ium-3-olate\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H13ClN4/c1-2-9-10(11(14)17-12(15)16-9)7-3-5-8(13)6-4-7/h3-6H,2H2,1H3,(H4,14,15,16,17)\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" umbrella\\n\",\n        \"output\": \" umbrella is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" raincoat\\n\",\n        \"output\": \" raincoat is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(3s)-2,6-dioxopiperidin-3-yl]undec-10-enamide\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H28N6O3S/c1-3-5-6-18-15-12-16(20-17(19-15)27-7-4-2)23(22-21-12)11-8-10(9-24)13(25)14(11)26/h10-11,13-14,24-26H,3-9H2,1-2H3,(H,18,19,20)/t10-,11-,13-,14+/m1/s1\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc2C(=O)C3=C(Nc2c1)C(=O)NN(Cc4cc5ccccc5s4)C3=O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5r)-3-[4-[1-[(2s)-2,3-dihydroxypropanoyl]-3,6-dihydro-2h-pyridin-4-yl]-3-fluorophenyl]-5-(1,2-oxazol-3-yloxymethyl)-1,3-oxazolidin-2-one\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][Ring2][C][N][C][C][S][C][C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H24N2O2/c1-3-20-7-10-22(11-8-20)18(13-20)19(23)15-6-9-21-17-5-4-14(24-2)12-16(15)17/h3-6,9,12,18-19,23H,1,7-8,10-11,13H2,2H3\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCC(=O)Nc1ccc2c3ccccc3C(=O)C(=O)c2c1\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc2c(C)cc(N[C@H]3CCC[C@@H](C3)NCc4cccc(OC(F)(F)F)c4)nc2c1\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H23Cl2N5O2/c1-28(2)11-16(29)12-30-17-6-4-15(5-7-17)26-20-10-21(25-13-24-20)27-19-9-14(22)3-8-18(19)23/h3-10,13,16,29H,11-12H2,1-2H3,(H2,24,25,26,27)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch1][S][=C][C][=C][Ring1][=Branch1][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1][N][N][=N][C][C][=C][Branch1][=Branch2][S][C][=Ring1][Branch1][C][Ring1][=Branch2][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC1=CC=C2C(=CC1=O)[C@H](CCc3cc(OC)c(OC)c(OC)c23)NC(=O)C\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" N(c1cccnc1)c2ncnc3ccccc23\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2c(Nc3cnc(NC(=O)c4ccccc4)nc3)ncnc2cc1OCCCN5CCOCC5\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(carbamoylamino)-5-phenylthiophene-3-carboxamide\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][N][=C][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][N][Ring2][Ring1][Branch1][Ring2][Ring1][C]\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" phenylmethyl n-[6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-2-thiophen-2-ylpyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][=Branch1][C][=O][N][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][S][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" c1cnc2cccnc2c1\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-ethyl-n',1,2-trimethyl-n-phenylpyrimidin-1-ium-4,6-diamine\\n\",\n        \"output\": \" -0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][Branch2][Ring1][=Branch2][C][C][N][Ring1][=Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[4-(2-chloro-4-fluorophenyl)piperazin-1-yl]-2-(pyridin-4-ylmethoxy)ethanone\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" pyridin-4-ylmethyl n-[2-(4-fluorophenyl)-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" catamaran\\n\",\n        \"output\": \" catamaran is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(CCN1CCCCC1)(C2CC3CC2C=C3)c4ccccc4\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-amino-8-(1h-pyrrol-2-yl)-2h-[1,2,4]triazolo[4,5-a]quinolin-1-one\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H15Cl2N3O3/c1-25-14-6-9-13(7-15(14)26-2)22-8-10(18(21)24)17(9)23-12-5-3-4-11(19)16(12)20/h3-8H,1-2H3,(H2,21,24)(H,22,23)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)C(=O)Cc1csc(NS(=O)(=O)c2cccc(Cl)c2C)n1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)[C@H](NC(=O)N(C)Cc1csc(n1)C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)OCc3cncs3)Cc4ccccc4\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H35N/c1-3-9-16(10-4-1)19(17-11-5-2-6-12-17)15-18-13-7-8-14-20-18/h16-20H,1-15H2\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)c1ccccc1O\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch2][Ring1][Branch2][C][O][C][C][Branch1][C][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" -0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=Branch1][O][C][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(3-hydroxy-6-oxoxanthen-9-yl)benzoic acid\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1nc(Br)cnc1NS(=O)(=O)c2ccc(Cl)s2\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)c1cccc(c1)c2ccc3c(C(=O)NCC45CC6CC(CC(C6)C4)C5)c(Cl)ccc3n2\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(1s)-1-(2,3-dimethylphenyl)ethyl]-1,3-dihydroimidazole-2-thione\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@][C][C][C][=Branch1][C][=O][C][=C][Ring1][#Branch1][C][C][C@H1][C@@H1][C][C][C@][Branch1][C][O][Branch1][#Branch1][C][=Branch1][C][=O][C][O][C@@][Ring1][#Branch2][Branch1][C][C][C][C][=Branch1][C][=O][C@H1][Ring2][Ring1][=Branch2][Ring1][S]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)CCCC(=O)Nc1ccc2C(=O)C(=O)c3ccccc3c2c1\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3,3-dimethyl-1h-indol-2-one\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-2-amino-3-(1h-indol-3-yl)propanoic acid\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(CCC(=O)O)c[nH]c1\\\\C=C\\\\2/C(=O)Nc3ccccc23\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)S(=O)(=O)NC2=CC=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C2=O)c3ccccc3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(C1CCCCC1)N2CC3N(CCc4ccccc34)C(=O)C2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)c1\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H22BrN3O2/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3/h8-9H,4-7,16H2,1-3H3,(H,17,19)\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H26F3N3O6/c1-16(2)24(25(37)28(29,30)31)33-23(36)15-34-21(18-6-4-3-5-7-18)13-12-20(26(34)38)32-22(35)14-17-8-10-19(11-9-17)27(39)40/h3-13,16,24H,14-15H2,1-2H3,(H,32,35)(H,33,36)(H,39,40)\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][O][C@][Branch1][N][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][N][Ring1][N][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" witness\\n\",\n        \"output\": \" witness is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch1][N][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCS(=O)(=O)c1ccc(Oc2cc3nc([nH]c3cc2CN4C(=O)CCC4=O)c5ccccn5)cc1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)NCc3ccccc3\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H19N3O/c1-2-17-7-9-18(10-8-17)15(19)14-11-12-5-3-4-6-13(12)16-14/h3-6,11,16H,2,7-10H2,1H3\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2cc(Nc3cc(Cl)ccc3Cl)ncn2)cc1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-methyl-3-(phenylmethoxy)pyran-4-one\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][N][C][=Branch1][C][=O][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][P][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][C][=C][Ring1][S]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10O3/c16-12-7-5-10(6-8-12)13-9-11-3-1-2-4-14(11)18-15(13)17/h1-9,16H\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H19BrN6O/c23-16-3-1-2-14(10-16)17-11-18(28-22-20(17)21(24)26-13-27-22)15-4-5-19(25-12-15)29-6-8-30-9-7-29/h1-5,10-13H,6-9H2,(H2,24,26,27,28)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C][=Branch1][Branch1][=C][C][Ring1][=Branch1][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=N][C][=Branch2][Ring2][S][=C][Branch1][=Branch1][N][C][Ring1][=Branch1][=O][C][=C][C][=C][Branch2][Ring1][N][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H26FN3O2/c1-13-17(9-15(10-18(13)23)21(28)26-16-6-7-16)19-8-5-14(11-24-19)20(27)25-12-22(2,3)4/h5,8-11,16H,6-7,12H2,1-4H3,(H,25,27)(H,26,28)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" thunderstorm\\n\",\n        \"output\": \" thunderstorm is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H]1C[C@H]2[C@@H]3CC[C@](O)(C(=O)C)[C@@]3(C)C[C@H](O)[C@]2(F)[C@@]4(C)C=CC(=O)C=C14\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(4-fluorophenyl)sulfonyl-n-[(4-methylphenyl)methyl]pyrrolidine-2-carboxamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCSCCCOCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" copyright\\n\",\n        \"output\": \" copyright is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H20N4/c1-5-19(13-9-7-6-8-10-13)15-11-14(16-3)18(4)12(2)17-15/h6-11H,5H2,1-4H3/p+1\\n\",\n        \"output\": \" -0.91\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m0/s1\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(3,4-dichlorophenyl)-n-[4-[(2,2-dimethylpropanoylamino)methyl]phenyl]-3-hydroxypiperidine-1-carboxamide\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][S][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2,3-dichlorophenyl)-(4-pyridin-2-ylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2r)-2-(3-chloro-4-methylsulfonylphenyl)-3-cyclopentyl-n-[5-[(1s)-1,2-dihydroxyethyl]pyrazin-2-yl]propanamide\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][O][C][C][Branch2][Ring1][=Branch1][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17)\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19N7O3S/c1-29-12-11-23-30(27,28)15-6-4-14(5-7-15)24-19-20-10-8-16(25-19)17-13-21-18-3-2-9-22-26(17)18/h2-10,13,23H,11-12H2,1H3,(H,20,24,25)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" viola\\n\",\n        \"output\": \" viola is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H18F4N4O3/c1-9(2)14(15(28)18(20,21)22)25-13(27)8-26-16(24-7-12(23)17(26)29)10-3-5-11(19)6-4-10/h3-7,9,14H,8,23H2,1-2H3,(H,25,27)\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)S(=O)(=O)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H5I2NO/c10-6-4-7(11)9(13)8-5(6)2-1-3-12-8/h1-4,13H\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][#Branch2][N][Branch1][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][#Branch2][C][N][C][C][C][O][C][C][O][C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)CC(N(C)C)C1(CCC1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H22N6O2/c1-2-7-24-20(28)19-17(22)16-6-3-5-15(18(16)25-26-19)13-10-14(12-23-11-13)21(29)27-8-4-9-27/h3,5-6,10-12H,2,4,7-9H2,1H3,(H2,22,25)(H,24,28)\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring2][Ring1][Ring1][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)C(c2ccc(O)cc2)C(Cl)(Cl)Cl\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-bis[(4-chlorophenyl)methyl]-2h-tetrazol-5-amine\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][C][Branch1][Ring1][C][C][=C][Ring1][Branch2][N][C][=Branch1][C][=O][N][C][C][NH1][N][=C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Ring2][Ring1][Branch1][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-chloro-n-[1-(2-hydroxyethyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)N1c2ccccc2C[C@H](O)c3ccccc13\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H24FN5O5S/c1-13(2)31-21(28)26-8-6-14(7-9-26)32-20-16-11-25-27(19(16)23-12-24-20)18-5-4-15(10-17(18)22)33(3,29)30/h4-5,10-14H,6-9H2,1-3H3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][=C][C][Branch2][Ring1][N][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][=N][NH1][N][=Ring1][Branch1][=C][C][C][C][C][C][Ring1][=Branch1][=N][Ring2][Ring1][=N]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOc1noc2cc(OCCC3CCN(CC3)c4ccc(C)nn4)ccc12\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C[C@H](c2ccccc2)c3cccc(N)c3C1\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-[(2s)-3-(5-chlorospiro[3h-1-benzofuran-2,4'-piperidine]-1'-yl)-2-hydroxypropoxy]-4-hydroxyphenyl]acetamide\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H23Cl2N5O2/c1-28(2)12-16(29)13-30-17-6-4-15(5-7-17)25-21-24-10-9-20(27-21)26-19-11-14(22)3-8-18(19)23/h3-11,16,29H,12-13H2,1-2H3,(H2,24,25,26,27)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch2][Ring1][Branch1][C][=C][Ring1][=Branch1][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][Branch1][C][O][C][N][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(1r)-1-[4-[(6-pyridin-4-ylquinazolin-2-yl)amino]phenyl]ethyl]acetamide\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(2-fluorophenyl)methyl]-2-pyridin-2-ylpyrimidine-4,6-diamine\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][S][C][=Branch1][C][=O][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][C][Ring1][Ring1]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H25ClN4O4/c1-29-19-11-15-17(12-20(19)30-10-4-9-28-7-2-3-8-28)25-13-26-23(15)27-21-16(24)5-6-18-22(21)32-14-31-18/h5-6,11-13H,2-4,7-10,14H2,1H3,(H,25,26,27)\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2cc(Nc3ccc(F)cc3F)ncn2)cc1\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(4-methoxyphenyl)methyl]-1h-pyrazole-3,5-diamine\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" drawbridge\\n\",\n        \"output\": \" drawbridge is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)n1c2ccccc2c3c(C)c(NC(=O)N4CCOCC4)ccc13\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](CO)Nc1nc(NCc2ccccc2)c3ncn(C(C)C)c3n1\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][N][=C][Branch1][C][N][S][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=Branch2][=C][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" colony\\n\",\n        \"output\": \" colony is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)CCNC(=O)c1c(C)[nH]c(\\\\C=C\\\\2/C(=O)Nc3ccc(Cl)cc23)c1C\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-pyridin-4-yl-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-(6-bicyclo[2.2.1]hept-2-enyl)-1-phenyl-3-piperidin-1-ylpropan-1-ol\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCC(=O)C1(CCN(CC1)C(=O)[C@@H](Cc2ccc(OC)cc2)NC(=O)[C@@H](N)Cc3cncn3C)c4ccccc4\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-[(1r)-2-[2-[3-[2-(2,3-dichlorophenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch2][Ring2][Branch2][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 4.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C@H1][Branch1][C][C][O][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Ring2][=C][Ring1][=N][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cccc(Cl)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" methyl n-[6-(benzoyl)-1h-benzimidazol-2-yl]carbamate\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(6-methoxynaphthalen-2-yl)butan-2-one\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CSc1ccc(cc1)C(=O)C(C)(C)N2CCOCC2\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][Branch2][Ring1][O][N][C][=N][C][=N][C][NH1][N][=C][Branch1][O][O][C][C][N][C][C][C][C][Ring1][Branch1][C][Ring1][P][=Ring1][=N][=C][C][=C][Ring2][Ring1][Branch2][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][C@@H1][Branch1][C][O][C][O][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(N1CCCCC1)c2scc3CCCCc23\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[1-[(3r)-3-(3,5-difluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n,n-dimethylpropan-1-amine\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" japanese\\n\",\n        \"output\": \" japanese is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" radish\\n\",\n        \"output\": \" radish is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc(N)c2nc(CO)cnc2n1\\n\",\n        \"output\": \" -0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(6,8-dimethoxy-4-methyl-2,3-dihydropyrrolo[3,2-c]quinolin-1-yl)phenol\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(9-ethylcarbazol-3-yl)-3-pyridin-4-ylpropanamide\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(Nc1ncnc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-hydroxy-3-phenyl-1h-indol-2-one\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][N][Ring1][=Branch2][C]\\n\",\n        \"output\": \" -1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-carbazol-9-ylpropanoic acid\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][N][C][Branch2][Ring1][=Branch1][C][C][=C][C][Branch1][Ring1][O][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][N][=N][C][=C][Branch1][C][N][N][=C][N][=C][Ring2][Ring1][#Branch1][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[5-fluoro-2-methyl-1-(4-methylsulfonylphenyl)sulfonylindol-3-yl]acetic acid\\n\",\n        \"output\": \" -0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][Branch1][C][Br][=C][C][=C][Ring1][#Branch1][O]\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-chloro-2-[(2-methyl-4-phenylsulfonylpiperazin-1-yl)methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[[2-amino-5-[(2,3-difluorophenyl)methylsulfanyl]-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]-2-methylpropan-1-ol\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H25N3O2/c1-14(2)24-18-7-5-4-6-16(18)20-15(3)17(8-9-19(20)24)22-21(25)23-10-12-26-13-11-23/h4-9,14H,10-13H2,1-3H3,(H,22,25)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)C2=COc3cc(O)ccc3C2=O\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H25N7O5/c1-33-23(32)28-8-9-30(20-4-5-25-22(27-20)29-7-6-24-14-29)17(13-28)11-21(31)26-12-16-2-3-18-19(10-16)35-15-34-18/h2-7,10,14,17H,8-9,11-13,15H2,1H3,(H,26,31)\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H28N4O3/c1-27(2,3)30-25(32)24(20-13-15-28-16-14-20)31(18-21-10-7-17-34-21)26(33)23-12-11-22(29-23)19-8-5-4-6-9-19/h4-17,24,29H,18H2,1-3H3,(H,30,32)\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][N][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9N3OS/c1-7(14)11-10-12-9(13-15-10)8-5-3-2-4-6-8/h2-6H,1H3,(H,11,12,13,14)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-phenylethoxy)ethoxy]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" workshop\\n\",\n        \"output\": \" workshop is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-fluoro-4-methoxy-8-(4-methylpiperazin-1-yl)-n-(4-morpholin-4-ylphenyl)quinoline-2-carboxamide\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" chain\\n\",\n        \"output\": \" chain is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-acetyl-7-hydroxychromen-2-one\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][P][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H15NO3/c20-16(21)12-11-15-19-17(13-7-3-1-4-8-13)18(22-15)14-9-5-2-6-10-14/h1-10H,11-12H2,(H,20,21)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCc1nc2c(N)nc3ccccc3c2s1\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][=C][O][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][=C][O][Ring1][S]\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H30N4O/c1-3-28(4-2)25(30)21-12-10-20(11-13-21)24(29-17-15-26-16-18-29)22-9-5-7-19-8-6-14-27-23(19)22/h5-14,24,26H,3-4,15-18H2,1-2H3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl (2s)-2-[[(2s)-1-[(2s)-2-cyclohexyl-2-[[(2s)-2-methylaminopropanoyl]amino]acetyl]pyrrolidine-2-carbonyl]amino]-3,3-di(phenyl)propanoate\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" bee\\n\",\n        \"output\": \" bee is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[(1r)-1-[3-(4-ethoxyphenyl)-4-oxoquinazolin-2-yl]ethyl]-n-(pyridin-3-ylmethyl)-2-[4-(trifluoromethyl)phenyl]acetamide\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H10ClN3O3/c16-12-4-2-1-3-10(12)15-11-7-9(19(21)22)5-6-13(11)18-14(20)8-17-15/h1-7H,8H2,(H,18,20)\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[[(4-methylpyridin-2-yl)amino]methyl]naphthalen-2-ol\\n\",\n        \"output\": \" 4.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H22FN3O7/c22-17-9-14(25-10-15(32-21(25)29)12-30-19-5-8-31-23-19)1-2-16(17)13-3-6-24(7-4-13)20(28)18(27)11-26/h1-3,5,8-9,15,18,26-27H,4,6-7,10-12H2/t15-,18+/m1/s1\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H7N3OS/c13-8(7-2-1-3-10-6-7)12-9-11-4-5-14-9/h1-6H,(H,11,12,13)\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H9N3O3/c15-13-11-10(9-2-1-4-19-9)12(8-3-5-18-6-8)20-14(11)17-7-16-13/h1-7H,(H2,15,16,17)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)c1nnn(c1N)c2ccccc2\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H10N2O3/c16-12-8-15(13(17)11-6-3-7-18-11)10-5-2-1-4-9(10)14-12/h1-7H,8H2,(H,14,16)\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[3-fluoro-5-(4-methoxyoxan-4-yl)phenoxy]methyl]-1-methylquinolin-2-one\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" feeling\\n\",\n        \"output\": \" feeling is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](CO)Nc1nc(SCc2ccccc2F)nc3NC(=O)Sc13\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][C][C][Branch1][C][C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][C][Ring1][#Branch1][=N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][P][Ring1][Branch2]\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl 4-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]benzoate\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[1-[(3r)-3-(3-chloro-5-fluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch2][Ring1][N][C@H1][Branch1][C][O][C][C][C][N][Branch1][=C][C][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring1][#C][=C][Ring2][Ring1][#Branch1][O][C]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-[[(1s,4s)-3,6-diazabicyclo[2.2.1]heptan-6-yl]methyl]benzamide\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H20N4O3/c22-18-4-1-5-19(11-18)25-20(26)17-8-6-15(7-9-17)13-24-21(27)28-14-16-3-2-10-23-12-16/h1-12H,13-14,22H2,(H,24,27)(H,25,26)\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1Nc2ccc(cc2C1=O)S(=O)(=O)N3CCC[C@H]3COc4ccccc4\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H13NO/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9H,10,14H2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][C][=C][Branch2][Ring2][Ring1][C][C][N][C][C][C][S][C][C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1][C][=C][Ring2][Ring1][=C]\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H22O2/c1-2-23(20-9-5-3-6-10-20)25(21-11-7-4-8-12-21)22-16-13-19(14-17-22)15-18-24(26)27/h3-18H,2H2,1H3,(H,26,27)/b18-15+,25-23-\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[3-[2-(2-naphthalen-1-ylethoxy)ethoxy]propylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(NC1CCCCC1)C2CCCN(C2)S(=O)(=O)c3cccs3\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)c1ccc2Oc3nc(N)c(cc3C(=O)c2c1)C(=O)O\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-hydroxy-2-phenylchromen-4-one\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-methoxy-8-(4-methyl-1,4-diazepan-1-yl)-n-(4-morpholin-4-ylphenyl)-4-oxo-1h-quinoline-2-carboxamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1=NS(=O)(=O)c2cc(Cl)ccc2N1\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H17N3S/c1-2-5-12-7-3-4-8-9(6-7)14-10(11)13-8/h7,12H,2-6H2,1H3,(H2,11,13)/t7-/m0/s1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H20N4/c1-4-13-19-14-15(20(13)9-10(2)3)11-7-5-6-8-12(11)18-16(14)17/h5-8,10H,4,9H2,1-3H3,(H2,17,18)\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-hydroxy-2-(4-hydroxyphenyl)isoindole-1,3-dione\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(C(=O)Nc2c(Cl)cncc2Cl)c3cccnc13\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(Sc3ccccc3)c(CC(=O)O)n2C\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16F5N3O2S/c18-14-4-1-5-15(19)12(14)11-28(26,27)25-9-7-24(8-10-25)16-13(17(20,21)22)3-2-6-23-16/h1-6H,7-11H2\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1cn(Cc2ccccc2)c3ccccc13\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-methyl-3-oxo-1,2,4-thiadiazol-5-yl)benzamide\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)Nc1ccc2Sc3ccccc3N(C(=O)CCN4CCOCC4)c2c1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNCC[C@@H](Oc1ccc(cc1)C(F)(F)F)c2ccccc2\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6,6-dimethyl-1-(4-methylsulfanylphenyl)-1,3,5-triazine-2,4-diamine\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" minibus\\n\",\n        \"output\": \" minibus is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H13Cl2N5/c16-11-3-1-8(5-12(11)17)7-20-9-2-4-13-10(6-9)14(18)22-15(19)21-13/h1-6,20H,7H2,(H4,18,19,21,22)\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][Branch1][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][N][Ring1][#Branch2][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)N(C)c2nc[nH]c2C1=O\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H21N5O4/c26-19(15-4-3-5-16(14-15)25(27)28)22-20-21-17-6-1-2-7-18(17)24(20)9-8-23-10-12-29-13-11-23/h1-7,14H,8-13H2,(H,21,22,26)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(4-chlorophenyl)methyl]indole-2,3-dione\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O-1][S+1][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][=C][C][=N][N][=N][N][Ring1][Branch1][N][=Ring1][=Branch2]\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=Branch1][C][=O][O][C][=C][C][C][C][N][C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][Ring1][S][Ring1][O]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][O][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][N][=Ring1][=N][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-[[4-[[3-chloro-4-(6-methylpyridin-3-yl)oxyphenyl]amino]-1h-pyrazolo[4,5-e]pyrimidin-3-yl]oxy]ethyl]piperidin-4-ol\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H34N2O/c1-21(2)19-27-20-24(25-15-9-10-16-25)18-26(23-13-7-4-8-14-23)17-22-11-5-3-6-12-22/h3-8,11-14,21,24H,9-10,15-20H2,1-2H3\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[3-(1-adamantylmethylcarbamoyl)-4-chlorophenyl]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C10H10F3N3/c11-10(12,13)7-2-1-3-8(6-7)16-5-4-9(14)15-16/h1-3,6H,4-5H2,(H2,14,15)\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-cyclopropyl-7-[(2s)-2-(dimethylaminomethyl)morpholin-4-yl]-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid\\n\",\n        \"output\": \" -0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccccc1Nc2oc(nn2)C(=O)Nc3ccc(Oc4cccnc4)nc3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-morpholin-4-ylpyrimido[2,3-a]isoquinolin-4-one\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-(2,4-difluorophenyl)-2-hydroxybenzoic acid\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-chloro-n-(cyclohexylmethyl)quinoline-5-carboxamide\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch2][Ring1][Ring2][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (6s,8s,9r,10s,11s,13s,14s,17r)-17-acetyl-9-fluoro-11,17-dihydroxy-6,10,13-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)NCc3cc[n+]([O-])cc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (7-dimethylaminophenothiazin-3-ylidene)-dimethylazanium\\n\",\n        \"output\": \" -0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][N]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=N][N][Branch1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][F][N][=Ring1][=N]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12N2S/c16-15(17)14-9-12-11(7-4-8-13(12)18-14)10-5-2-1-3-6-10/h1-9H,(H3,16,17)\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H10ClN5/c11-8-14-9(12)16-10(15-8)13-6-7-4-2-1-3-5-7/h1-5H,6H2,(H3,12,13,14,15,16)\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1,3-dimethyl-7h-purine-2,6-dione\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(NC(=O)CCC2CCCCC2)cc1NC(=O)c3ccc(O)cc3\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2-phenylethyl)-2-[2,3,4-trihydroxy-5-(methyl-(3-phenylpropyl)sulfamoyl)benzoyl]-3,4-dihydro-1h-isoquinoline-7-sulfonamide\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H15N7O2S/c1-18-27(25,26)13-6-4-12(5-7-13)22-17-19-10-8-14(23-17)15-11-20-16-3-2-9-21-24(15)16/h2-11,18H,1H3,(H,19,22,23)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(1r,2r)-2-[(2,3-dichloro4h-thieno[2,3-d]pyrrole-5-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]acetic acid\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=N][C][Branch1][=C][C][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][C][=Branch1][Ring2][=N][Ring1][#C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H]1[C@@H]2CN(CCN3CCOCC3)CC[C@H]2Cc4[nH]c5ccc(cc5c14)C(F)(F)F\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][C@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][C][=C][Branch1][C][Cl][S][C][=Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H25N5O2/c1-26(2)14-18(27)15-28-19-10-8-17(9-11-19)24-21-22-13-12-20(25-21)23-16-6-4-3-5-7-16/h3-13,18,27H,14-15H2,1-2H3,(H2,22,23,24,25)\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14FN3O2/c1-21-14-7-12-13(8-15(14)22-2)18-9-19-16(12)20-11-5-3-10(17)4-6-11/h3-9H,1-2H3,(H,18,19,20)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H17F2N3O5/c20-15-7-13(8-16(21)18(15)12-1-4-23(11-25)5-2-12)24-9-14(29-19(24)26)10-27-17-3-6-28-22-17/h1,3,6-8,11,14H,2,4-5,9-10H2/t14-/m1/s1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C][C][Ring1][Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)S(=O)(=O)c1ccc(cc1)c2cc(ccc2OCC(=O)O)C(F)(F)F\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" ON(C=O)C1(CS(=O)(=O)N2CCN(CC2)c3ccc(F)cc3)CCOCC1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H12O3/c17-15-8-9-18-16-10-13(6-7-14(15)16)19-11-12-4-2-1-3-5-12/h1-10H,11H2\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(2-chlorophenyl)methyl]-2-(phenoxy)benzamide\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H19F6N3O5S/c1-11(2)16(17(31)19(21,22)23)27-15(30)10-29-14(12-6-4-3-5-7-12)9-8-13(18(29)32)28-35(33,34)20(24,25)26/h3-9,11,16,28H,10H2,1-2H3,(H,27,30)\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)Nc1nc(ns1)c2ccccc2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H17FN6O3/c19-12-2-1-3-13(10-12)22-18-24-23-17(28-18)16(26)21-14-4-5-15(20-11-14)25-6-8-27-9-7-25/h1-5,10-11H,6-9H2,(H,21,26)(H,22,24)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][Branch1][#Branch2][C][C][=C][C][=C][N][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H17F2N3O2/c21-16-7-3-13(4-8-16)18-23-19(27-24-18)15-2-1-11-25(12-15)20(26)14-5-9-17(22)10-6-14/h3-10,15H,1-2,11-12H2/t15-/m0/s1\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,6-dichloro-n-[4-chloro-3-(2-dimethylaminoethoxy)phenyl]-4-(trifluoromethyl)benzenesulfonamide\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H20FN5O3/c1-13-12-14(6-7-17(13)26-8-10-28-11-9-26)22-18(27)19-24-25-20(29-19)23-16-5-3-2-4-15(16)21/h2-7,12H,8-11H2,1H3,(H,22,27)(H,23,25)\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[4-[4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]phenyl]piperazin-1-yl]-2-hydroxyethanone\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H26FN5O4/c24-15-1-3-19-18(11-15)29(22(31)14-33-19)10-9-28-7-5-16(6-8-28)25-12-17-2-4-20-23(26-17)27-21(30)13-32-20/h1-4,11,16,25H,5-10,12-14H2,(H,26,27,30)\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(1h-benzimidazol-2-yl)propyl]-1h-benzimidazole\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H15NO2S/c16-14(17)11-19(18)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15H,11H2,(H2,16,17)\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)COc1ccc(Cl)cc1C2CCCCC2\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3,4-dichlorophenyl)-4-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]piperazine-1-carboxamide\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-methyl-n-[4-(trifluoromethyl)phenyl]-1,2-oxazole-4-carboxamide\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][S][C][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][S][C][=Branch1][C][=O][N][C][C@H1][Branch1][C][O][C][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1][C][=C][C][=C][O][C][C][O][C][Ring1][=Branch1][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[(3s)-3-(3,4-dichlorophenyl)-3-[2-(4-phenyl-1-azoniabicyclo[2.2.2]octan-1-yl)ethyl]piperidin-1-yl]-2-(3-propan-2-yloxyphenyl)ethanone\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)c1ncn2c1CN(C)C(=O)c3cc(F)ccc23\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccccc1CN(C(=O)C)c2cnccc2Oc3ccccc3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C@@H1][Branch2][Ring2][Branch1][N][C][=C][Branch2][Ring1][=Branch1][N][C][=C][C][=C][C][Branch1][#Branch2][C][=Branch1][C][=O][N][Branch1][C][C][C][=C][Ring1][O][O][C][=Branch1][C][=O][C][Ring2][Ring1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Cl][=C][Branch1][C][N][C][=C][Ring1][Branch2][O][C]\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H15N3/c1-12(13-7-3-2-4-8-13)19-16-14-9-5-6-10-15(14)17-11-18-16/h2-12H,1H3,(H,17,18,19)\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1cc(Cl)c2c3C(=O)NNC(=O)c3[nH]c2c1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][O][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][O][C][N][C][=N][C][=C][C][=N][Ring1][=Branch1][C][C][Ring1][=C][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cccc(F)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H10N2O2S/c14-16(15,11-6-2-1-3-7-11)13-10-5-4-8-12-9-10/h1-9,13H\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][N][=C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][C][=Ring1][S]\\n\",\n        \"output\": \" -0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" FC1(F)Oc2ccc(\\\\C=C\\\\3/SC(=O)NC3=O)cc2O1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)c1nc(nc(n1)N(C)C)N(C)C\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H10O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-8,16-17H\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(1s)-1-[[1-[(4-chlorophenyl)methyl]2,3-dihydroindole-7-carbonyl]amino]ethyl]benzoic acid\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3cccc(Cl)c3n1CC(=O)O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" ethyl n-[10-(3-morpholin-4-ylpropanoyl)phenothiazin-2-yl]carbamate\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-chloro-3-([1,3]oxazolo[4,5-b]pyridin-2-yl)aniline\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 9-[(2,6-dichlorophenyl)methyl]-n,n-diethylpurin-6-amine\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][Branch1][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][Branch1][#C][N][=C][C][=C][Branch1][C][C][C][=C][N][Ring1][#Branch2][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C1CC(CCN1)c2ccccc2\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H14N4O2S/c1-7-4-8(2)14-12(13-7)19-6-11(17)15-10-5-9(3)18-16-10/h4-5H,6H2,1-3H3,(H,15,16,17)\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [F][C][Branch1][C][F][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][=N][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H23ClN2O/c19-16-14(2-1-3-15(16)20)17(22)21-10-18-7-11-4-12(8-18)6-13(5-11)9-18/h1-3,11-13H,4-10,20H2,(H,21,22)\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(C)cccc34\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H12N2O/c1-17-9-6-7-13-11(8-9)14(15)10-4-2-3-5-12(10)16-13/h2-8H,1H3,(H2,15,16)\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(cc(OC)c1OC)C(=O)Nc2ccc(Cl)c(c2)c3nc4ccccc4[nH]3\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(Cl)cc1NC(=O)Nc2cnccn2\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" FC(F)(F)c1nnc2ccc(NCc3cccnc3)nn12\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)c1ccc(Oc2cccc3cccnc23)c(c1)[N+](=O)[O-]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)C1CCN(CC(=O)Nc2ccc3OCOc3c2)CC1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n'-propan-2-ylpyridine-4-carbohydrazide\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H31BrCl2N4O2/c1-3-35-31-24(18-4-6-20(27)7-5-18)19-8-12-33(13-9-19)26(2)10-14-32(15-11-26)25(34)23-21(28)16-30-17-22(23)29/h4-7,16-17,19H,3,8-15H2,1-2H3/b31-24+\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-bromo-2-methyl-3-[1-(2-methyl-5-nitrophenyl)sulfonylpyrazol-3-yl]imidazo[1,2-a]pyridine\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2]\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=N][N][C][=Branch1][C][=O][N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][N][Branch1][=C][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][Cl][C][=Branch1][C][=O][C][=C][Ring1][S]\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H6ClN3/c8-5-3-1-2-4-6(5)10-11-7(4)9/h1-3H,(H3,9,10,11)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-chloro-3h-1,3-benzoxazol-2-one\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][N][=N][N][Branch1][Branch1][C][=Ring1][Branch1][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[6-(3-methylaminopyrrolidin-1-yl)pyridin-3-yl]-4-phenylbenzamide\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)Oc1cccc(CC(=O)N2CCC[C@@](CC[N+]34CCC(CC3)(CC4)c5ccccc5)(C2)c6ccc(Cl)c(Cl)c6)c1\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 11-[2-(4-methylpiperazin-1-yl)acetyl]-5h-pyrido[2,3-b][1,4]benzodiazepin-6-one\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][=C][Branch1][C][N][S][N+1][=Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][C][=C][C][=N][S][N][=C][Ring1][Branch1][C][=Ring1][=Branch2][N][C][=N][C][C][N][Ring1][Branch1]\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H21FN2O3/c18-15-3-1-13(2-4-15)16(21)14-5-7-19(8-6-14)17(22)20-9-11-23-12-10-20/h1-4,14H,5-12H2\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H36N4O5S/c1-26(2,28)25(33)29-22(18-36-17-20-9-5-4-6-10-20)24(32)30-15-13-27(14-16-30)19-31(37(3,34)35)23-12-8-7-11-21(23)27/h4-12,22H,13-19,28H2,1-3H3,(H,29,33)/t22-/m1/s1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)c1sc(cc1N)c2ccccc2\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NC(=O)CN3CCOCC3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H18ClNO4S/c1-3-23-17(20)12-19(16-7-5-4-6-13(16)2)24(21,22)15-10-8-14(18)9-11-15/h4-11H,3,12H2,1-2H3\\n\",\n        \"output\": \" 4.03\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H19N3O3S/c1-21(16-4-2-3-9-19-16)10-11-24-14-7-5-13(6-8-14)12-15-17(22)20-18(23)25-15/h2-9,15H,10-12H2,1H3,(H,20,22,23)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H16FN5O2S/c1-11-2-7-14(18)15(10-11)22-16-8-9-20-17(23-16)21-12-3-5-13(6-4-12)26(19,24)25/h2-10H,1H3,(H2,19,24,25)(H2,20,21,22,23)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-(4-amino-2-ethylimidazo[4,5-c]quinolin-1-yl)butyl]methanesulfonamide\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][O][C][=Branch1][N][=C][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" nigeria\\n\",\n        \"output\": \" nigeria is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19NO3S/c1-12-4-9-17-16(10-12)19(13(2)20(17)11-18(21)22)24-15-7-5-14(23-3)6-8-15/h4-10H,11H2,1-3H3,(H,21,22)\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H23N3O4S/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21)\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[3-(1h-benzimidazol-2-yl)-4-chlorophenyl]-3,4,5-trimethoxybenzamide\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" chin\\n\",\n        \"output\": \" chin is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNCCC(Oc1ccc(cc1)C(F)(F)F)c2ccccc2\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C][N][C][C][=C][C][Branch1][C][Br][=C][C][=C][Ring1][#Branch1][O][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][#C][O][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][=N][C][Branch2][Ring1][Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1][=N][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H25N7O2S/c1-28(2)14-5-12-25-32(30,31)18-9-7-17(8-10-18)26-22-23-13-11-19(27-22)20-16-24-21-6-3-4-15-29(20)21/h3-4,6-11,13,15-16,25H,5,12,14H2,1-2H3,(H,23,26,27)\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(NC(=O)CSc2nnc(C)n2c3ccc(C)cc3)cc1\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)N=C1C=C2N(c3ccc(Cl)cc3)c4ccccc4N=C2C=C1Nc5ccc(Cl)cc5\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3ccc(F)cc3F)c2cc1OC\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][N][C][C][Branch1][C][O][C][O][C][=N][S][N][=C][Ring1][Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (5-methyl-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1cc(Cl)cc(Cl)c1\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-phenyl-3a,4-dihydro-3h-chromeno[4,3-c]pyrazole\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][C][C][C][C][Ring1][=Branch1][=N][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4cc(ccc34)C(F)(F)F\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H19N3OS/c1-21-12-14-11-15(19-7-9-20-10-8-19)18-16(17-14)13-5-3-2-4-6-13/h2-6,11H,7-10,12H2,1H3\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" frog\\n\",\n        \"output\": \" frog is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (8r,9s,13s,14s,17s)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][C][N][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][N][S][Ring1][N]\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(2-methylpropyl)imidazo[4,5-c]quinolin-4-amine\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-chloro-3-(4-chlorophenyl)sulfanyl-2-methylpyrrolo[3,2-c]pyridin-1-yl]acetic acid\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[1-(4-chlorophenyl)cyclobutyl]-n,n,3-trimethylbutan-1-amine\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" bat\\n\",\n        \"output\": \" bat is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCc1nc2c(N)nc3ccccc3c2n1CCCCNS(=O)(=O)C\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(C1CCN(CCC(c2ccccc2)c3ccc(cc3)S(=O)(=O)C)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H20ClN3O4/c1-29-19-10-13(11-20(30-2)21(19)31-3)23(28)25-14-8-9-16(24)15(12-14)22-26-17-6-4-5-7-18(17)27-22/h4-12H,1-3H3,(H,25,28)(H,26,27)\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][S][O][C][=C][C][Branch2][Ring1][Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1][=N][C][=N][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch2][O][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(4-chloro-2-fluorophenyl)-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(2s)-2-(phenoxymethyl)pyrrolidin-1-yl]sulfonyl-1h-indole-2,3-dione\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(1,5-dimethyl-3-phenylsulfanylindol-2-yl)acetic acid\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H13N3/c1-2-6-11(7-3-1)10-15-14-16-12-8-4-5-9-13(12)17-14/h1-9H,10H2,(H2,15,16,17)\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H17F2N5O3/c20-13-3-1-2-4-15(13)23-19-25-24-18(29-19)17(27)22-12-5-6-16(14(21)11-12)26-7-9-28-10-8-26/h1-6,11H,7-10H2,(H,22,27)(H,23,25)\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H14O2/c1-15(17,13-10-6-3-7-11-13)14(16)12-8-4-2-5-9-12/h2-11,17H,1H3\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [(8r,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] propanoate\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=N][C][Branch1][=Branch2][C][C][=C][C][=C][C][=Ring1][=Branch1][=C][Ring1][O][C][=N][C][C][Branch1][C][N][=N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16ClN3O3S/c1-10-8-11-4-2-3-5-14(11)20(10)19-16(21)12-6-7-13(17)15(9-12)24(18,22)23/h2-7,9-10H,8H2,1H3,(H,19,21)(H2,18,22,23)\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-ethyl-2-hydroxypyrano[3,2-c]quinoline-4,5-dione\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(3-methyl-5-phenylimidazol-4-yl)-[1,3]thiazolo[4,5-e]pyrimidin-7-amine\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H31Cl2N3O4S/c1-17-3-5-21(6-4-17)35(32,33)28-25(31)30-13-9-19(10-14-30)29-15-11-20(12-16-29)34-23-8-7-22(26)18(2)24(23)27/h3-8,19-20H,9-16H2,1-2H3,(H,28,31)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc2[nH]ncc2c1\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C37H48N6O5S2/c1-24(2)33(42-36(46)43(5)20-29-22-49-35(40-29)25(3)4)34(45)39-28(16-26-12-8-6-9-13-26)18-32(44)31(17-27-14-10-7-11-15-27)41-37(47)48-21-30-19-38-23-50-30/h6-15,19,22-25,28,31-33,44H,16-18,20-21H2,1-5H3,(H,39,45)(H,41,47)(H,42,46)/t28-,31-,32-,33-/m0/s1\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-[5-(cyclopropylcarbamoyl)-3-fluoro-2-methylphenyl]-n-(2,2-dimethylpropyl)pyridine-3-carboxamide\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[(2s)-2-[(phenylamino)methyl]pyrrolidin-1-yl]sulfonyl-1h-indole-2,3-dione\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][C][C][C][=C][C][Branch1][=C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][=C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Branch2][C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" cyclopentyl n-[1-[[2-methoxy-4-(phenylsulfonylcarbamoyl)phenyl]methyl]indazol-6-yl]carbamate\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H17FN4O2/c1-2-22-15(21)19-12-7-8-13(20-14(12)17)18-9-10-3-5-11(16)6-4-10/h3-8H,2,9H2,1H3,(H,19,21)(H3,17,18,20)\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch2][Ring2][#Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring1][=Branch2][C][C][C][Branch1][C][C][=N][N][Branch1][Ring2][C][C][O][C][=Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring2][Ring1][=Branch1][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 4.29\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H24N2O4S/c1-5-17(6-2)10-9-16-15(18)13-11-12(22(4,19)20)7-8-14(13)21-3/h7-8,11H,5-6,9-10H2,1-4H3,(H,16,18)\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" minute\\n\",\n        \"output\": \" minute is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2,3-difluorophenyl)-2-[5-[[7-[3-(2-hydroxyethyl-propylamino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C6H9N3O3/c1-5-7-4-6(9(11)12)8(5)2-3-10/h4,10H,2-3H2,1H3\\n\",\n        \"output\": \" -0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-2-amino-n-[(e,3s)-5-phenyl-1-phenylsulfonylpent-1-en-3-yl]propanamide\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C@@H1][Branch1][O][N][C][=Branch1][C][=O][C][Branch1][C][Cl][Cl][C@H1][Branch1][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (s)-(5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(2-fluorophenyl)amino]-n-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1cc(nc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H28N4O4S/c1-14(2)12-29-24-21(22(31)27(3)25(29)33)20(23(32)28-9-8-16(30)13-28)19(34-24)10-15-11-26-18-7-5-4-6-17(15)18/h4-7,11,14,16,26,30H,8-10,12-13H2,1-3H3/t16-/m1/s1\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1nccnc1NS(=O)(=O)c2ccc(N)cc2\\n\",\n        \"output\": \" -0.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H11Cl2F3N2O/c1-8(14(23)22-11-4-2-10(16)3-5-11)13-12(17)6-9(7-21-13)15(18,19)20/h2-8H,1H3,(H,22,23)\\n\",\n        \"output\": \" 4.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" move\\n\",\n        \"output\": \" move is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=Branch1][C][=O][N][Branch1][Branch1][C][=C][Ring1][#Branch1][C@@H1][O][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C][Ring1][Branch2][Branch1][C][F][F]\\n\",\n        \"output\": \" -1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-(4-fluorophenoxy)-2-methyl-3-[[(3s)-1-propan-2-ylpiperidin-3-yl]methyl]quinazolin-4-one\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[(2,5-dimethoxyphenyl)methyl]-4-(phenoxy)-1h-pyrazolo[4,5-c]pyridin-3-amine\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" apparel\\n\",\n        \"output\": \" apparel is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=N][C][=N][C][=Branch1][#Branch1][=N][N][Ring1][=Branch2][Ring1][Branch1][C][=Branch1][C][=O][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [7-amino-3-(benzoyloxy)-5,6,7,8-tetrahydronaphthalen-2-yl] benzoate\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)N(C)C(=O)[C@@]1(Cc2ccccc2)CCCN(C1)C(=O)[C@@H](Cc3c[nH]c4ccccc34)NC(=O)C(C)(C)N\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][=C][NH1][C][=Ring1][#Branch2][\\\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][\\\\-Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(c1ccccc1)c2cc(NC)[n+](C)c(C)n2\\n\",\n        \"output\": \" -0.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H19N3O/c1-12-19-9-10-21(12)11-13-7-8-16-17(18(13)22)14-5-3-4-6-15(14)20(16)2/h3-6,9-10,13H,7-8,11H2,1-2H3\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H20N2O2/c19-16(20-11-10-18-8-4-1-5-9-18)14-12-17-15-7-3-2-6-13(14)15/h2-3,6-7,12,17H,1,4-5,8-11H2\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc(ccc1Cn2ccc3ccc(NC(=O)OC4CCCC4)cc23)C(=O)NS(=O)(=O)c5ccccc5\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][C][C][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C@H1][Branch1][C][O][C][N][C][C][=C][C][=C][C][Branch1][Ring1][O][C][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" sign\\n\",\n        \"output\": \" sign is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H21N3O3S2/c1-2-7-15-13(18)11-21-14-6-5-12(10-16-14)22(19,20)17-8-3-4-9-17/h5-6,10H,2-4,7-9,11H2,1H3,(H,15,18)\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][S][C][Branch2][Ring1][Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][Ring1][P]\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-ethylbutyl)-3-[[2-methoxy-4-[(2-methylphenyl)sulfonylcarbamoyl]phenyl]methyl]-1-methylindole-5-carboxamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[[2-(4-chlorophenyl)-2-methylpropanoyl]amino]-n-(4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H13N3OS/c1-19-13-9-7-11(8-10-13)14-17-15(16)20-18(14)12-5-3-2-4-6-12/h2-10,16H,1H3/p+1\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)c1ncnc2nc[nH]c12\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-methylcyclohexyl)-n-quinolin-5-ylacetamide\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(OC(=O)N2CCN3CCC2CC3)cc1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (6s)-6-hydroxy-5,6-dihydrobenzo[b][1]benzazepine-11-carboxamide\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCCSCCOCCc1cccc2ccccc12)c3ccc(O)c4NC(=O)Sc34\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(NC(=O)CCc2c(C)nc3nc(C)nn3c2C)cc1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H28FN7O2/c1-15(2)31-16(3)25-13-20(31)22-19(24)12-26-23(28-22)27-17-4-6-18(7-5-17)29-8-10-30(11-9-29)21(33)14-32/h4-7,12-13,15,32H,8-11,14H2,1-3H3,(H,26,27,28)\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-methoxy-1-methyl-9h-pyrido[3,4-b]indole\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C@H1][Branch1][C][O][C][=Branch1][C][=O][N][C][C][C][=Branch1][Branch1][=C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][N][C][C@H1][Branch1][#Branch2][C][O][C][C][=C][O][N][=Ring1][Branch1][O][C][Ring1][N][=O]\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)NC(=O)NS(=O)(=O)c1cnccc1Nc2cccc(C)c2\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H11FN4/c1-7-6-10(16-11(13)14-7)15-9-4-2-8(12)3-5-9/h2-6H,1H3,(H3,13,14,15,16)\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][Branch2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][O][C][=N][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1h-1-benzazepine-2,5-dione\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)Nc1ccc2cnn(c3cncc(n3)n4ccc(CC(=O)O)c4)c2c1\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)[C@H](NC(=O)CCc1ccccc1)C(=O)N2CCCC2\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CC)S(=O)(=O)c1ccc(NC(=O)[C@@](C)(O)C(F)(F)F)c(Cl)c1\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H24N2O2/c22-18-13-20(19(23)15-7-2-1-3-8-15)12-17-16-9-5-4-6-14(16)10-11-21(17)18/h4-6,9,15,17H,1-3,7-8,10-13H2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 8-chloro-1-methyl-6-phenyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=N][C][Branch1][C][N][=N][C][Branch1][C][N][=C][Ring1][Branch2][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=N][C][=Branch1][Ring2][=N][Ring1][#Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21FN6O/c1-11(2)26-12(3)22-10-16(26)17-15(20)9-23-19(25-17)24-14-7-5-13(6-8-14)18(27)21-4/h5-11H,1-4H3,(H,21,27)(H,23,24,25)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-dimethylaminopropyl)-4-[(4-imidazo[3,2-a]pyridin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H15ClN4O3S/c19-14-7-10-6-11(22-17(10)27-14)16(25)21-12-5-9-3-1-2-4-13(9)23(18(12)26)8-15(20)24/h1-4,6-7,12,22H,5,8H2,(H2,20,24)(H,21,25)\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C@H1][Branch1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-dimethylaminopropyl)-4-[(4-imidazo[2,3-f]pyridazin-3-ylpyrimidin-2-yl)amino]benzenesulfonamide\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1c(NCC2CCNCC2)nccc1C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C29H30N4O5S/c1-38-27-16-21(29(35)32-39(36,37)25-9-3-2-4-10-25)11-12-23(27)19-33-26-17-24(14-13-22(26)18-30-33)31-28(34)15-20-7-5-6-8-20/h2-4,9-14,16-18,20H,5-8,15,19H2,1H3,(H,31,34)(H,32,35)\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](NC1=NC(=O)[C@@](C)(S1)C(F)(F)F)c2ccccc2F\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H22N2O5/c30-26(29-25-12-11-21(16-28-25)27(31)32)22-13-23(33-17-19-7-3-1-4-8-19)15-24(14-22)34-18-20-9-5-2-6-10-20/h1-16H,17-18H2,(H,31,32)(H,28,29,30)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(2-phenylethoxy)propylsulfanyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(carbamoylamino)-5-phenyl-n-[(3s)-piperidin-3-yl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18FN3O4/c20-13-4-6-14(7-5-13)23-19(21)17(9-22-23)18(26)12-2-1-3-16(8-12)27-11-15(25)10-24/h1-9,15,24-25H,10-11,21H2/t15-/m0/s1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(3,4-dimethoxyphenyl)-n-(6-methoxy-1,3-benzothiazol-2-yl)propanamide\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccnc(NC2CCN(CC2)C(=O)c3ccccc3)c1\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[(2,3-dimethylphenyl)amino]benzoic acid\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring2][C][C][O][C][C][C][C][Branch1][C][C][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(2,4-difluorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)S(=O)(=O)c1ccc2Sc3ccccc3\\\\C(=C\\\\CCN4CCN(C)CC4)\\\\c2c1\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCOCCCNCCc1cccc(Cl)c1)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H22FN5/c1-27(2)13-12-24-21-14-19(16-6-4-3-5-7-16)25-22-15-20(26-28(21)22)17-8-10-18(23)11-9-17/h3-11,14-15,24H,12-13H2,1-2H3\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H33N3O3S2/c1-2-17-4-6-18(7-5-17)10-12-25-11-3-14-31-15-13-26-16-21(29)19-8-9-20(28)22-23(19)32-24(30)27-22/h4-9,21,25-26,28-29H,2-3,10-16H2,1H3,(H,27,30)/t21-/m0/s1\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3,4-dihydro-1h-isoquinoline-2-carboximidamide\\n\",\n        \"output\": \" -1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cccc(c1)[C@@H](C)NCCCc2ccccc2Cl\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H27ClN4O2/c1-5-27(6-2)10-9-24-22(29)20-13(3)19(25-14(20)4)12-17-16-11-15(23)7-8-18(16)26-21(17)28/h7-8,11-12,25H,5-6,9-10H2,1-4H3,(H,24,29)(H,26,28)/b17-12-\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-6-methoxy-1,4-benzoxazin-3-one\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H15N3O2/c1-21-12-8-6-11(7-9-12)10-15(20)19-16-17-13-4-2-3-5-14(13)18-16/h2-9H,10H2,1H3,(H2,17,18,19,20)\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H11NO3/c15-11-5-1-9(2-6-11)13(17)14-10-3-7-12(16)8-4-10/h1-8,15-16H,(H,14,17)\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)Nc1ccc(O)cc1OC[C@@H](O)CN2CCC3(CC2)Cc4cc(Cl)ccc4O3\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][B][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=O]\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][O][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][N][C][=C][N][=C][C][=C][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][=Branch2][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)C1Cc2c([nH]c3ccccc23)C(N1)c4ccccc4\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H28O5S/c28-23(19-31-24-12-10-22(11-13-24)27(29)30)20-32-25-14-16-26(17-15-25)33-18-6-2-5-9-21-7-3-1-4-8-21/h1,3-4,7-8,10-17H,2,5-6,9,18-20H2,(H,29,30)\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H11N3OS/c1-5-3-6(2)11-8(10-5)13-4-7(9)12/h3H,4H2,1-2H3,(H2,9,12)\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H21N3O4/c1-2-14-19(20(26)21(23)27)18-15(9-6-10-16(18)28-12-17(22)25)24(14)11-13-7-4-3-5-8-13/h3-10H,2,11-12H2,1H3,(H2,22,25)(H2,23,27)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[di(phenyl)methylsulfinyl]acetamide\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch2][Ring1][=Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [(1r,5s)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate\\n\",\n        \"output\": \" -0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(2-fluorophenyl)amino]-n-(4-morpholin-4-ylphenyl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(CN(CCN(C)C)c2ccccn2)cc1\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,17+,19+,20+,21+,22+/m1/s1\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[2-[(3-phenyl-[1,2,4]triazolo[3,4-f]pyridazin-6-yl)amino]ethyl]benzenesulfonamide\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCn1cnc(c2ccccc2)c1c3nc4c(N)ncnc4s3\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C35H36ClNO3S/c1-34(2,40)30-9-4-3-7-25(30)13-17-32(41-23-35(18-19-35)22-33(38)39)27-8-5-6-24(20-27)10-15-29-16-12-26-11-14-28(36)21-31(26)37-29/h3-12,14-16,20-21,32,40H,13,17-19,22-23H2,1-2H3,(H,38,39)/b15-10+/t32-/m1/s1\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-oxo-4-(4-phenylphenyl)butanoic acid\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1C=C(C(=O)O)C(=O)c2ccc(C)nc12\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[2-(phenylmethylsulfanyl)ethyl]benzamide\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H21F3N2O5S/c21-20(22,23)16-6-7-18(30-14-19(26)27)15(12-16)13-24-8-10-25(11-9-24)31(28,29)17-4-2-1-3-5-17/h1-7,12H,8-11,13-14H2,(H,26,27)\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (4as,11s,11ar)-11-methyl-2-(2-morpholin-4-ylethyl)-9-(trifluoromethyl)-1,3,4,4a,5,6,11,11a-octahydropyrido[4,3-b]carbazole\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H30N4O4/c1-31-21-4-2-18-3-5-25(30)29(22(18)15-21)11-10-28-8-6-19(7-9-28)26-16-20-14-23-24(17-27-20)33-13-12-32-23/h2-5,14-15,17,19,26H,6-13,16H2,1H3\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-chloro-2-(pyridin-4-ylmethyl)-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc(cc1)c2cc(C(=O)N3CCOCC3)c4cc(C)ccc4n2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][Cl]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(difluoromethyl)-1h-benzimidazole\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-(3-hydroxypropylsulfanyl)-3-methyl-1-(2-methylpropyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" o5-methyl o3-(2-methylpropyl) 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C@@H1][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][=C][C][Branch2][Ring1][Ring1][N][C][=C][C][=N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][O][Ring1][#Branch1][=C][C][=C][Ring2][Ring1][C][O]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][Branch1][P][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=N][N][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Branch2][Ring1][Ring1][C][=C][Branch1][#Branch2][C][=C][Ring1][=Branch1][C][Branch1][C][C][C][C][Branch1][C][C][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H16N2O/c1-15(2)7-11-13(12(18)8-15)14(16)9-5-3-4-6-10(9)17-11/h3-6H,7-8H2,1-2H3,(H2,16,17)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)CCCc1ccc(cc1)N(CCCl)CCCl\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 4-[(2s)-3-(3-carbamimidoylphenyl)-2-[[2,4,6-tri(propan-2-yl)phenyl]sulfonylamino]propanoyl]piperazine-1-carboxylate\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H23ClN2/c1-21(2)12-5-13-22-18-7-4-3-6-15(18)8-9-16-10-11-17(20)14-19(16)22/h3-4,6-7,10-11,14H,5,8-9,12-13H2,1-2H3\\n\",\n        \"output\": \" 3.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][C][=C][Branch1][Branch2][C][N][C][C][C][Ring1][Ring2][C][=C][Ring1][O][F]\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-[(1r)-2-[3-[2-[2-(2,3-dichlorophenyl)ethylamino]ethylsulfanyl]propylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C(=O)O)c1cccc(Oc2ccccc2)c1\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" cardboard\\n\",\n        \"output\": \" cardboard is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][Branch2][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][N][=N][NH1][N][=Ring1][Branch1][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H32FN3O/c1-17(2)25-28-24-12-9-21(20-7-10-22(27)11-8-20)14-23(24)26(31)30(25)16-19-6-5-13-29(15-19)18(3)4/h7-12,14,17-19H,5-6,13,15-16H2,1-4H3/t19-/m0/s1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C25H29N3O3S/c1-17(2)14-28-21-16-27(15-19-10-6-9-18-8-4-5-11-20(18)19)24(32-13-7-12-29)22(21)23(30)26(3)25(28)31/h4-6,8-11,16-17,29H,7,12-15H2,1-3H3\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCCC(COc2nccc(Nc3cc(NC(=O)c4ccnc(c4)N5CCOCC5)ccc3C)n2)C1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C(=O)Nc1ccc(Cl)cc1)c2ncc(cc2Cl)C(F)(F)F\\n\",\n        \"output\": \" 4.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc2C=CC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2c1\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(OC2CCN(CC2)C3CCN(CC3)S(=O)(=O)NC(=O)c4ccccc4)cc1Cl\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCCCC1CCN2c3ccccc3Sc4ccc(cc24)[S+](C)[O-]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H15NO2S/c20-22(21,16-11-5-2-6-12-16)19-18-14-8-7-13-17(18)15-9-3-1-4-10-15/h1-14,19H\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOc1ccc(CCNCCCSCCNC[C@H](O)c2ccc(O)c3NC(=O)Sc23)cc1\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][Branch2][Ring1][=C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O][C][C][C][C][C][C][Ring2][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1C2CCCCC2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][Branch1][C][C][N][Branch1][C][C][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][=Branch2][=C][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=N][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][Branch1][C][F][Branch1][C][F][C][=C][C][Branch2][Ring1][#Branch1][C][O][C][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=Branch1][Branch1][=C][Ring2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][Branch1][#Branch2][C][N][C][C][N][C][C][Ring1][=Branch1][=C][C][=Ring1][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][Branch1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=C][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][N][C][=Branch1][C][=O][C][=N][N][=C][C][=Branch1][=C][=C][Branch1][C][F][C][=C][C][Ring1][#Branch1][=C][Ring1][O][N][C][=C][C][=C][Branch1][Ring1][O][C][C][=C][Ring1][Branch2][O][C]\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C@@H1][S][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][Branch2][C][C][N][Branch1][C][C][C][C][=Branch1][C][=O][C@@H1][Ring1][P][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C@H1][Branch2][Ring2][=Branch2][C][C@H1][Branch1][C][O][\\\\C][=C][\\\\C][=C][Branch2][Ring1][Branch2][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][C][Ring1][Ring1][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" FC(F)(F)c1cccc(c1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)c(Cl)c4\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][Branch1][=N][N][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-chloro-6-fluoro-1h-benzimidazole\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H](COc1cn2ncnc(Oc3ccc4[nH]c(C)cc4c3F)c2c1C)OC(=O)[C@H](C)N\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1c(cnn1c2ccc(F)cc2)C(=O)c3cccc(OC[C@H](O)CO)c3\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H24N2O2/c1-4-5-10-16-14-8-6-13(7-9-14)15(18)19-12-11-17(2)3/h6-9,16H,4-5,10-12H2,1-3H3\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CCCC4\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H5ClN2/c8-6-1-2-7-5(3-6)4-9-10-7/h1-4H,(H,9,10)\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(N)(COP(=O)(O)O)C(=O)O\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C8H7BrN4/c9-4-1-2-6-5(3-4)7(10)13-8(11)12-6/h1-3H,(H4,10,11,12,13)\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Oc2ccc(Cl)cc2)c3cc(F)ccc3n1CC(=O)O\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)c1ccc2N=C3C=CC(=[N+](C)C)C=C3Sc2c1\\n\",\n        \"output\": \" -0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H11N3/c1-8-7-10(11)13(12-8)9-5-3-2-4-6-9/h2-7H,11H2,1H3\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1NC(=O)c3ccc4ncccc4c3\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C1CN2CCC1C(C2)c3ccc(cc3)c4ccccc4\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-chloro-n-[1-[3-hydroxy-2-(hydroxymethyl)propyl]-2-oxo-3,4-dihydroquinolin-3-yl]-1h-indole-2-carboxamide\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H27ClN4O5/c1-15(2)34-20-12-16(31-10-7-29-5-8-30-9-6-29)11-18-21(20)24(27-13-26-18)28-22-17(25)3-4-19-23(22)33-14-32-19/h3-4,11-13,15H,5-10,14H2,1-2H3,(H,26,27,28)\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][Branch1][C][C][=C][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch2][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][C][=C][Ring1][=C][Ring1][=Branch1][N][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H21NO3S/c1-10(2)9-12-5-7-13(8-6-12)11(3)14(16)15-19(4,17)18/h5-8,10-11H,9H2,1-4H3,(H,15,16)/t11-/m0/s1\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H11ClN6OS2/c15-7-2-1-3-8-10(7)23-14(19-8)24-13-20-9-11(16)17-6-18-12(9)21(13)4-5-22/h1-3,6,22H,4-5H2,(H2,16,17,18)\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H9Cl2F2N3OS/c20-11-2-1-3-12(21)17(11)18-14-5-7-16(25-26(14)9-24-19(18)27)28-15-6-4-10(22)8-13(15)23/h1-9H\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][C][=C][S][C][Branch2][Ring1][Branch1][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][Ring1][P]\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-chloro-9-[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]purin-2-amine\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2-aminobenzimidazol-1-yl)-phenylmethanone\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(phenoxy)-n-(phenylmethyl)pyridine-3-carboxamide\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-methyl-n-(1,3-thiazol-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidine-2-carboxamide\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC1(CCOCC1)c2cc(F)cc(OCc3ccc4N(C)C(=O)C=Cc4c3)c2\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H17FN4O2/c23-16-11-5-7-13-18(16)25-22(29)27-20-21(28)24-17-12-6-4-10-15(17)19(26-20)14-8-2-1-3-9-14/h1-13,20H,(H,24,28)(H2,25,27,29)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(Nc1ccccc1)N2CCOCC2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[[4-[(2-fluoro-5-methylphenyl)amino]pyrimidin-2-yl]amino]benzenesulfonamide\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H13ClFNO4S/c1-10-17(25(23,24)13-5-2-11(18)3-6-13)14-8-12(19)4-7-15(14)20(10)9-16(21)22/h2-8H,9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" -0.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COCCCOc1ccnc(C[S+]([O-])c2nc3ccccc3[nH]2)c1C\\n\",\n        \"output\": \" -0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1h-benzimidazol-2-ylmethanamine\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1=NC(=C(NC1=O)c2ccc(CN3CCC(CC3)N4C(=O)Nc5ccccc45)cc2)c6ccccc6\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[(2,4-dichlorophenyl)methyl]-6-oxopyridine-3-carboxamide\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-n-[(1-hydroxycycloheptyl)methyl]-5-[4-[(2r)-2-hydroxy-3-methoxypropyl]-3,5-dioxo-1,2,4-triazin-2-yl]benzamide\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1cccc2c3ccccc3C(=O)C(=O)c12\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC4CCN(C)CC4\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=N][N][C][=Branch1][C][=O][C][S][C][=N][N][=C][Branch1][C][C][N][Ring1][=Branch1][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch1][C][N][C][=Branch1][C][=O][N][C@@H1][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][\\\\C][=C][\\\\S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H24Cl2N2O4/c1-15-12-25(13-17-10-18(23)6-7-20(17)30-14-22(28)29)8-9-26(15)21(27)11-16-4-2-3-5-19(16)24/h2-7,10,15H,8-9,11-14H2,1H3,(H,28,29)/t15-/m0/s1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-nitro-7,8,9,10-tetrahydro-6h-azepino[1,2-a]benzimidazole\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4,6-dichloro-3-[(e)-(2-oxo-1-phenylpyrrolidin-3-ylidene)methyl]-1h-indole-2-carboxylic acid\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1cc(O)cc(\\\\C=C\\\\c2ccc(O)c(O)c2)c1\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][O][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-pyridin-3-ylquinazolin-4-amine\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccc(cc1)C2CNCCc3c(Cl)c(O)c(O)cc23\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H9N5/c1-12(2)7-5-6(9-3-8-5)10-4-11-7/h3-4H,1-2H3,(H,8,9,10,11)\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" ethyl 2-[2-[(4-chlorophenyl)sulfonylamino]-1,3-thiazol-4-yl]benzoate\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[3-(azepan-1-yl)propyl]-n-(1,3-benzodioxol-5-ylmethyl)-3-(3,5-difluorophenyl)-1,2-oxazol-5-amine\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-(3-hydroxypropylsulfanyl)-3-methyl-1-(2-methylpropyl)-6-(naphthalen-1-ylmethyl)pyrrolo[3,4-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 4.36\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=N][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H17N3O/c1-10-12(14(2)3)13(17)16(15(10)4)11-8-6-5-7-9-11/h5-9H,1-4H3\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)c1[nH]c2ccccc2c1CC(=O)Nc3cccc(c3)C(F)(F)F\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H27NO3/c1-2-14-22-15-18(23)16-25-21-11-7-6-10-19(21)20(24)13-12-17-8-4-3-5-9-17/h3-11,18,22-23H,2,12-16H2,1H3/t18-/m0/s1\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H14N4S2/c1-18-17-15(13-7-4-10-23-13)20-14(12-6-3-9-22-12)11-5-2-8-19-16(11)21-17/h2-10,15H,1H3,(H,18,19,21)\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H28ClN3O3S2/c23-16-4-1-3-15(13-16)7-9-24-8-2-11-30-12-10-25-14-19(28)17-5-6-18(27)20-21(17)31-22(29)26-20/h1,3-6,13,19,24-25,27-28H,2,7-12,14H2,(H,26,29)/t19-/m0/s1\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" dinghy\\n\",\n        \"output\": \" dinghy is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5,7-diiodoquinolin-8-ol\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch1][C][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H](N)COc1c(C)cccc1C\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][#C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-[(4-methoxyphenyl)sulfonylamino]-2-oxo-6-phenylpyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H29F2N7O/c1-14(2)33-15(3)27-13-21(33)22-20(26)12-28-24(31-22)30-17-5-6-18(19(25)11-17)23(34)29-16-7-9-32(4)10-8-16/h5-6,11-14,16H,7-10H2,1-4H3,(H,29,34)(H,28,30,31)\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11N5/c13-11-10-12(15-7-14-11)17(8-16-10)6-9-4-2-1-3-5-9/h1-5,7-8H,6H2,(H2,13,14,15)\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H20N2S/c1-13(18(2)3)12-19-14-8-4-6-10-16(14)20-17-11-7-5-9-15(17)19/h4-11,13H,12H2,1-3H3\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H25NO2/c1-22-17-5-3-2-4-16(17)18(21)20-12-19-9-13-6-14(10-19)8-15(7-13)11-19/h2-5,13-15H,6-12H2,1H3,(H,20,21)\\n\",\n        \"output\": \" 4.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H31N5O/c1-3-30-12-14-31(15-13-30)18-20-16-19(2)25(28-17-20)21-8-10-22(11-9-21)26(32)29-24-7-5-4-6-23(24)27/h4-11,16-17H,3,12-15,18,27H2,1-2H3,(H,29,32)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCC(N1NC(=O)C2=C(C1=O)C(=O)c3ccc(Cl)cc3N2)c4ccncc4\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(carbamoylamino)-n-methyl-5-phenylthiophene-3-carboxamide\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1h-indazol-6-amine\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1cccc2ccccc12\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H24N4O3S/c1-13(2,3)14-8-10(18)9-20-12-11(15-21-16-12)17-4-6-19-7-5-17/h10,14,18H,4-9H2,1-3H3/t10-/m0/s1\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(9-methylcarbazol-3-yl)-3-pyridin-4-ylpropanamide\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(4-methoxyphenyl)-1,2-benzothiazol-3-one\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-amino-5-phenylthiophene-3-carboxamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)C5CCNCC5\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)[C@H](CCc1ccccc1)N[C@@H](C)C(=O)N2[C@H]3CCC[C@H]3C[C@H]2C(=O)O\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H8Cl2O4S/c14-11-7(13(18)9-2-1-5-20-9)3-4-8(12(11)15)19-6-10(16)17/h1-5H,6H2,(H,16,17)\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C4H10NO6P/c1-4(5,3(6)7)2-11-12(8,9)10/h2,5H2,1H3,(H,6,7)(H2,8,9,10)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cn1cc(cc1C=O)C(=O)CCCCOc2ccc(cc2)C(=O)O\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(carbamoylamino)-5-(4-fluorophenyl)-n-[(3s)-piperidin-3-yl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=N][C][=C][C][Branch1][P][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][Ring1][Ring1][S]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4,6-dimethyl-7,8,9,10-tetrahydropyrano[6,5-f]quinolin-2-one\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch2][Ring1][Branch2][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][N][C][=Branch1][C][=O][C][N][=C][Branch1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl][C][Ring1][#C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Brc1ccc(s1)N2C[C@@]3(CN4CCC3CC4)OC2=O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C@H1][Branch2][Ring2][=Branch2][N][C][=Branch1][C][=O][C][=C][Branch2][Ring1][#Branch1][C][=Branch1][N][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H10O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-9,16H\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (5r)-3-(5-bromothiophen-2-yl)spiro[1,3-oxazolidine-5,8'-1-azabicyclo[2.2.2]octane]-2-one\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=N][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1][=N][Ring1][P]\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][N][=C][Branch1][Branch1][N][C][C][N][C][=N][C][=C][Branch1][C][C][N][Ring1][=Branch1][C][Ring1][=C][=C][Ring2][Ring1][C]\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27N7O2S/c1-28(2)14-6-15-29(3)33(31,32)19-10-8-18(9-11-19)26-23-24-13-12-20(27-23)21-17-25-22-7-4-5-16-30(21)22/h4-5,7-13,16-17H,6,14-15H2,1-3H3,(H,24,26,27)\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(N[C@H]1CN2CCC1CC2)c3ccc(s3)c4ccccc4\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H23F2N3O3/c1-15(29-23(32)13-16-11-17(27)14-18(28)12-16)25(33)30-24-21-9-4-3-7-19(21)20-8-5-6-10-22(20)31(2)26(24)34/h3-12,14-15,24H,13H2,1-2H3,(H,29,32)(H,30,33)/t15-,24?/m0/s1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ncnc2oc(c3cocc3)c(c4occc4)c12\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCC(CC1)Oc2cccc3ncnc(Nc4ccc(OCc5cnccn5)c(Cl)c4)c23\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H30ClFN4O3/c1-16-13-33(17(2)12-32(16)14-18-6-8-19(29)9-7-18)26(35)21-10-20-22(25(34)27(36)30(3)4)15-31(5)24(20)11-23(21)28/h6-11,15-17H,12-14H2,1-5H3/t16-,17+/m0/s1\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H11N/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(1,3-benzodioxol-5-yloxy)-6-(4-imidazol-1-ylphenoxy)pyrimidine\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1CCN(Cc2cnc(c(C)c2)c3ccc(cc3)C(=O)Nc4ccccc4N)CC1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H8O4/c14-7-5-9(15)12-11(6-7)17-10-4-2-1-3-8(10)13(12)16/h1-6,14-15H\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccnc(NCc2ccccc2O)c1\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" propan-2-yl 4-[5-methoxy-6-[(2-methyl-6-methylsulfonylpyridin-3-yl)amino]pyrimidin-4-yl]oxypiperidine-1-carboxylate\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C(Cc1nc2ccccc2[nH]1)c3nc4ccccc4[nH]3)c5ccccc5\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-bromonaphthalen-1-ol\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOC(=O)N1CCN(CC1)C(=O)[C@H](Cc2cccc(c2)C(=N)N)NS(=O)(=O)c3c(cc(cc3C(C)C)C(C)C)C(C)C\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)C(CO)c3ccccc3\\n\",\n        \"output\": \" -0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H28N4O4S/c1-15(2)13-17-9-11-18(12-10-17)21-19(23(29)25-4)7-6-8-20(21)33(30,31)28-22-24(32-5)27-16(3)14-26-22/h6-12,14-15H,13H2,1-5H3,(H,25,29)(H,26,28)\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=Branch2][Ring1][Branch1][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][Br][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7h-pyrrolo[3,2-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2cn(Cc3cccc4ccccc34)cc12\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][N][=C][C][=C][Branch1][P][N][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][=C][C][Ring1][S][=N][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H25F3N4O5/c1-16(2)21(22(35)26(27,28)29)32-20(34)14-33-23(18-11-7-4-8-12-18)30-13-19(24(33)36)31-25(37)38-15-17-9-5-3-6-10-17/h3-13,16,21H,14-15H2,1-2H3,(H,31,37)(H,32,34)\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n'-di(phenyl)pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CCCN2c3ccccc3Sc4ccc(cc24)C(F)(F)F)CC1\\n\",\n        \"output\": \" 4.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=C(CCN2CCC(CC2)c3noc4cc(F)ccc34)C(=O)N5CCCCC5=N1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3ccc(F)cc3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C2CCC1CC(C2)OC(=O)C(CO)c3ccccc3\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(OC2CCN(CC2)C3CCN(CC3)C(=O)NS(=O)(=O)c4ccccc4)cc1Cl\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1Nc2ccc(cc2C1=O)S(=O)(=O)N3CCC[C@H]3CNc4ccccc4\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H27Cl2N3O3/c27-23-6-5-19(15-24(23)28)34-18-9-13-30(14-10-18)17-7-11-31(12-8-17)26(33)22-16-29-25(32)21-4-2-1-3-20(21)22/h1-6,15-18H,7-14H2,(H,29,32)\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring1][O][C@@H1][Branch1][C][C][N][Branch1][#Branch2][C][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][=C][N][C@H1][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H22N4/c1-16(17-9-3-2-4-10-17)18(24-27-21-13-7-8-14-22(21)28-24)15-23-25-19-11-5-6-12-20(19)26-23/h2-14,16,18H,15H2,1H3,(H,25,26)(H,27,28)\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CC1)c2nc(NCCNc3ccc(cc3)[N+](=O)[O-])c4ccccc4n2\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=C][S][C][Branch1][P][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][O][N][=C][Ring1][=Branch1][C][=N][Ring1][#C]\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H28O3/c1-20-9-5-15(23)13-14(20)3-4-16-17(20)6-10-21(2)18(16)7-11-22(21)12-8-19(24)25-22/h3-4,13,16-18H,5-12H2,1-2H3/t16-,17+,18+,20+,21+,22-/m1/s1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2-(4-chlorophenyl)-1,3-thiazol-4-yl]acetic acid\\n\",\n        \"output\": \" -0.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][C@@H1][Branch1][C][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][Ring1][N]\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" N(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ncc(CO)c(CO)c1O\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)c1cc(nc2ccc(F)cc12)c3ccncc3\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-1-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl]pyrrolidine-2-carboxamide\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C11H12N2O2S/c1-7(13(15)11(12)14)10-6-8-4-2-3-5-9(8)16-10/h2-7,15H,1H3,(H2,12,14)\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H18FN3O4/c20-13-4-6-14(7-5-13)23-19(21)17(9-22-23)18(26)12-2-1-3-16(8-12)27-11-15(25)10-24/h1-9,15,24-25H,10-11,21H2/t15-/m1/s1\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H31F3N2O3/c1-5-33(6-2)17-18-36-25-16-15-24(19-26(25)35-4)32(3)27(34)22-9-7-20(8-10-22)21-11-13-23(14-12-21)28(29,30)31/h7-16,19H,5-6,17-18H2,1-4H3\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC(=O)CCc1ccc(OCc2cccc(Oc3ccccc3)c2)cc1\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)c1ccc(cc1)c2ccc(Cl)c(c2)C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" headline\\n\",\n        \"output\": \" headline is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-chloro-2-[[(3s)-4-[2-(3-chlorophenyl)acetyl]-3-methylpiperazin-1-yl]methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H14BrN3/c18-11-6-7-15-14(10-11)16(19)13-8-9-21(17(13)20-15)12-4-2-1-3-5-12/h1-7,10H,8-9H2,(H2,19,20)\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-(4-chlorophenoxy)-2-methyl-5-(trifluoromethyl)indol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H22Cl2FN5O/c1-12(19-16(22)2-3-17(24)20(19)23)30-18-8-13(9-27-21(18)25)14-10-28-29(11-14)15-4-6-26-7-5-15/h2-3,8-12,15,26H,4-7H2,1H3,(H2,25,27)/t12-/m1/s1\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C(=O)O)c1ccc2oc(nc2c1)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch1][=N][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=Branch1][#C][=C][C][=C][Ring1][=Branch1][N][Ring1][P][C][C][=Branch1][C][=O][O][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (5-fluoro-1h-indol-2-yl)-(4-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)C(C)C(=O)c1ccccc1\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [S][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H13BrN4O2/c18-14-10-19-17(21-13-8-6-11(7-9-13)16(23)24)22-15(14)20-12-4-2-1-3-5-12/h1-10H,(H,23,24)(H2,19,20,21,22)\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][N][Ring1][=C][C][C][Branch1][C][C][Branch1][C][C][O]\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H25N5O3S/c1-15-11-18-12-17(3)22-25-26-24(29(22)19(18)13-16(15)2)33-14-21(30)27-6-8-28(9-7-27)23(31)20-5-4-10-32-20/h4-5,10-13H,6-9,14H2,1-3H3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(N)COc1c(C)cccc1C\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H21N3O3/c1-26-16-6-4-5-14(13-16)19(24)22-11-9-15(10-12-22)23-18-8-3-2-7-17(18)21-20(23)25/h2-8,13,15H,9-12H2,1H3,(H,21,25)\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" ethyl (2s)-3-(4-hydroxyphenyl)-2-(naphthalene-1-carbonylamino)propanoate\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H21NO3S/c17-15-11-20(18,19)10-14(15)16-8-6-13(7-9-16)12-4-2-1-3-5-12/h1-5,13-15,17H,6-11H2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[(3-chlorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(4-methoxyphenyl)pyrimidin-2-amine\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]piperazin-1-yl]ethanol\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(4-hydroxyphenyl)-2h-chromen-7-ol\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 8-(4-phenylphenyl)-1-azabicyclo[2.2.2]octane\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H12N2O3/c17-13(18)11-8-4-5-9-12(11)16-14(19)15-10-6-2-1-3-7-10/h1-9H,(H,17,18)(H2,15,16,19)\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][Ring1][S][=Ring1][N]\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-hydroxy-1,2-di(phenyl)ethanone\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][=C][C][C][=C][N][=C][Branch1][C][N][N][=C][Ring1][#Branch1][N][=C][C][Branch1][Ring1][O][C][=C][Ring1][P][O][C]\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][C][O][=C][C][Branch1][C][O][=C][Ring1][Branch2][C][Ring1][N][=O]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H23N3O5S/c1-30-21-13-12-18(15-22(21)31-2)32(28,29)26-17-10-7-16(8-11-17)9-14-23(27)25-20-6-4-3-5-19(20)24/h3-15,26H,24H2,1-2H3,(H,25,27)/b14-9+\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H18N2O5/c1-2-25-18(22)16(19-17(21)14-6-4-3-5-7-14)12-13-8-10-15(11-9-13)20(23)24/h3-11,16H,2,12H2,1H3,(H,19,21)/t16-/m0/s1\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch1][=C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][Ring1][#Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(5,5-dioxodibenzothiophen-2-yl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Clc1ccc(cc1)C(=O)N[C@H]2CN3CCC2CC3\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H22F3N3O3S/c1-12(2)11-28-20-17(18(29)26-21(28)31)16(19(30)27-8-5-9-27)15(32-20)10-13-6-3-4-7-14(13)22(23,24)25/h3-4,6-7,12H,5,8-11H2,1-2H3,(H,26,29,31)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-1-naphthalen-1-yloxy-3-(propan-2-ylamino)propan-2-ol\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(N1CCNCC1)c2cc3ccccc3[nH]2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][=C][Branch1][C][O][C][=Branch2][Ring1][#Branch1][=C][C][=C][Ring1][#Branch1][O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(CCc1cccc(OCc2ccc3ccccc3n2)c1)CC(=O)O\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H12N6S3/c9-7-13-11-5(16-7)1-3-15-4-2-6-12-14-8(10)17-6/h1-4H2,(H2,9,13)(H2,10,14)\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H23ClN4O3/c22-17-2-1-15(26-20(29)25-18(27)10-24-26)6-16(17)19(28)23-11-21-7-12-3-13(8-21)5-14(4-12)9-21/h1-2,6,10,12-14H,3-5,7-9,11H2,(H,23,28)(H,25,27,29)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H27NO2/c1-18(2)13-16(17(19)11-5-4-6-12-17)14-7-9-15(20-3)10-8-14/h7-10,16,19H,4-6,11-13H2,1-3H3\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1-phenylethyl)quinazolin-4-amine\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [6-methyl-2-(4-methylphenyl)quinolin-4-yl]-morpholin-4-ylmethanone\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]-3-(2-pyrrolidin-1-ylethoxy)-1h-pyrazolo[4,5-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1cccc2cn[nH]c12\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1C=C(Oc2c1cccc2c3ccccc3)N4CCOCC4\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" margin\\n\",\n        \"output\": \" margin is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s)-1-[4-[(5-cyclopropyl-1h-pyrazol-3-yl)amino]pyrrolo[2,1-f][1,2,4]triazin-2-yl]-n-(6-fluoropyridin-3-yl)-2-methylpyrrolidine-2-carboxamide\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-chloro-n-(4-fluorophenyl)-1-oxidopyridin-1-ium-3-carboxamide\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H21N5O4/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14/h3-4,9-11H,5-8H2,1-2H3,(H2,20,21,22)\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][Branch1][Ring2][C][C][O][C][C][C][O][C][=C][C][=C][C][Branch2][Ring1][=C][N][C][C][=C][Branch2][Ring1][Ring1][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][NH1][N][=Ring1][P][=N][C][=N][C][Ring2][Ring1][Branch2][=C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][N][=C][Ring1][#C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[2-dimethylamino-1-(4-methoxyphenyl)ethyl]cyclohexan-1-ol\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C][C][C][C][C][C][Branch1][Ring2][C][Ring1][Branch2][N][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H10O2/c16-15-13(11-6-2-1-3-7-11)10-12-8-4-5-9-14(12)17-15/h1-10H\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=Branch1][=C][=C][C][=C][Ring1][=Branch1][C][=C][C][O][C][C][Ring1][=Branch1][N][C][C@H1][Branch1][#Branch2][C][O][C][C][=C][O][N][=Ring1][Branch1][O][C][Ring1][N][=O]\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[6-(benzoylamino)pyridin-2-yl]benzamide\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-n-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide\\n\",\n        \"output\": \" -0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (5-chloro-1h-indol-2-yl)-piperazin-1-ylmethanone\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-ethyl-n-[1-[(3r)-3-(3-fluorophenyl)-3-(4-methylsulfonylphenyl)propyl]piperidin-4-yl]-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][C][C][=C][Branch1][Branch2][C][Branch1][C][C][=C][Ring1][Branch2][S][=Branch1][C][=O][=Branch1][C][=O][N][Branch1][C][C][C][C][O][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Ring2][Ring1][=Branch1][=O]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccccc1NC(=O)NC2N=C(c3ccccc3)c4ccccc4NC2=O\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@@H1][Branch1][#Branch2][C][=N][C][=N][C][=C][Ring1][=Branch1][F][C@][Branch1][C][O][Branch1][=Branch2][C][N][C][=N][C][=N][Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][Ring1][O][=C][Ring1][S]\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C][N][C][C][N][Branch2][Ring1][O][C][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#C][Ring1][#Branch1][C][C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=C][C][=Branch2][Ring2][P][=N][C][=C][C][=C][Branch2][Ring1][P][N][C][=C][C][=Branch1][=Branch2][=N][C][Branch1][C][N][=N][Ring1][#Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring2][Ring1][N][Ring2][Ring1][Branch2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1(CN2CCC1CC2)c3ccc(cc3)c4ccccc4\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC1CCN(C1)c2ccc(NC(=O)c3ccc(cc3)c4ccccc4)cn2\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[4-(3,4-dimethoxyphenyl)-1,3-thiazol-2-yl]-3,5-dimethyl-1,2-oxazole-4-carboxamide\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" bongo\\n\",\n        \"output\": \" bongo is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-methyl-1-(2-methylpropyl)-6-(naphthalen-1-ylmethyl)pyrrolo[3,4-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 4.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1,2-di(phenyl)ethanamine\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(CN2C(=O)C(=O)c3ccccc23)cc1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n-methylpropan-1-amine\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H32ClNO2/c1-4-29(5-2)18-19-31-26-16-12-24(13-17-26)27(30,23-10-6-21(3)7-11-23)20-22-8-14-25(28)15-9-22/h6-17,30H,4-5,18-20H2,1-3H3\\n\",\n        \"output\": \" 3.98\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1c(N2C[C@@H]3CCCN[C@@H]3C2)c(F)cc4C(=O)C(=CN(C5CC5)c14)C(=O)O\\n\",\n        \"output\": \" -0.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(3-fluoro-4-phenylphenyl)propanoic acid\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][N][C][C][C][N][Branch1][Branch1][C][C][Ring1][#Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H11NO2S/c1-17-11-8-6-10(7-9-11)15-14(16)12-4-2-3-5-13(12)18-15/h2-9H,1H3\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch2][O][C][C][=Branch1][C][=O][O][C][=Branch1][Ring2][=C][Ring1][O][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][=Branch2]\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCCCOC(=O)NC1=NC(=O)N(C=C1F)[C@@H]2O[C@H](C)[C@@H](O)[C@H]2O\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chlorobenzamide\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3,3,3-trifluoro-2-hydroxy-2-methyl-n-(4-pyridin-3-ylsulfonylphenyl)propanamide\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring1][O][C][N][C][=Branch1][C][=O][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3,5-dichlorophenol\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3,3,3-trifluoro-n-[4-(4-fluorophenyl)sulfonylphenyl]-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H14ClF3N2O4S/c1-3-6-18-24(22,23)8-4-5-10(9(14)7-8)19-11(20)12(2,21)13(15,16)17/h3-5,7,18,21H,1,6H2,2H3,(H,19,20)/t12-/m1/s1\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H12Cl2O4/c1-3-7(2)13(18)8-4-5-9(12(15)11(8)14)19-6-10(16)17/h4-5H,2-3,6H2,1H3,(H,16,17)\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(cc1C(=O)NCC23CC4CC(CC(C4)C2)C3)N5CCNCC5\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][N][C][=C][C][=N][C][Ring1][=Branch1][=N][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][Branch1][C][C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[S+]([O-])CCN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][#Branch2][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][C][=C][C][=Branch1][C][=O][O][C][Ring1][#Branch1][=C][Ring1][O]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][Branch1][#Branch1][N][=C][Ring1][#C][Ring1][#Branch1][N][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H6Cl2N2O2S2/c10-6-1-2-7(11)8(5-6)17(14,15)13-9-12-3-4-16-9/h1-5H,(H,12,13)\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccccc1CCNC(=O)c2cc(ccc2Cl)N3N=CC(=O)NC3=O\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][N][C][=Branch1][C][=O][N][Branch1][S][C][C][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][Ring1][#Branch2][C][C][=C][S][C][=Ring1][Branch1][C][Ring2][Ring1][Branch1][=O]\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r,3r,4s,5r)-2-[6-amino-2-(phenylmethylsulfanyl)purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C@@H1][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][C][C@H1][Branch2][Ring1][Ring2][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-methyl-1,2,3,5-tetrahydro-1,5-benzodiazepin-4-one\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H13N3OS/c17-13-3-1-2-4-14(13)19-15(20)11-5-7-12(8-6-11)16-18-9-10-21-16/h1-10H,17H2,(H,19,20)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H11ClN4O3/c18-9-4-5-11-12(7-9)20-14-13(15(11)23)17(25)22(21-16(14)24)8-10-3-1-2-6-19-10/h1-7H,8H2,(H,20,23)(H,21,24)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1N(C(=O)c2ccccc2)c3ccccc3NC1=O\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (4-ethylpiperazin-1-yl)-(1h-indol-2-yl)methanone\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(1-benzofuran-2-yl)-1-azabicyclo[2.2.2]oct-2-ene\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC[C@H](O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][N][C][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4,5-dichlorobenzene-1,3-disulfonamide\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" grease\\n\",\n        \"output\": \" grease is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H21ClN2O3S/c1-4-23(14(3)25)17-6-5-7-18-20(17)21(13(2)24(18)12-19(26)27)28-16-10-8-15(22)9-11-16/h5-11H,4,12H2,1-3H3,(H,26,27)\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H13ClFN3O2/c1-22-14-6-10-13(7-15(14)23-2)19-8-20-16(10)21-9-3-4-12(18)11(17)5-9/h3-8H,1-2H3,(H,19,20,21)\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][S][N][C][=C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring1][P]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H14FN5O/c14-3-1-7-6-17-12(20)8-5-10(18-11(7)8)9-2-4-16-13(15)19-9/h2,4-5,7,18H,1,3,6H2,(H,17,20)(H2,15,16,19)/t7-/m0/s1\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)OC(=O)C1=CN(Cc2c(F)cccc2F)c3sc(c(CN(C)Cc4ccccc4)c3C1=O)c5ccc(NC(=O)C(C)C)cc5\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-oxo-6-phenyl-3-(pyridin-2-ylmethylcarbamoylamino)pyridin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H26F3N5O4/c1-16(2)22(23(36)26(27,28)29)33-21(35)15-34-20(18-8-4-3-5-9-18)11-10-19(24(34)37)32-25(38)31-14-17-7-6-12-30-13-17/h3-13,16,22H,14-15H2,1-2H3,(H,33,35)(H2,31,32,38)\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=C][C][=C][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][C][C][=Branch1][C][=O][O][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)(C)NCC(O)COc1nsnc1N2CCOCC2\\n\",\n        \"output\": \" -0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-phenylquinazolin-4-amine\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][Branch1][S][C][=Branch1][C][=O][N][C][=N][C][=C][Branch1][C][C][S][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][S][Ring2][Ring1][Ring2][=Branch1][C][=O][=O]\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCCSc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" freighter\\n\",\n        \"output\": \" freighter is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring2][=Branch2][C][N][C][=N][C][=Branch1][N][=N][C][=N][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C@H1][C][C][C][C][N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][P]\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(C1CCN(CC[C@H](c2ccc(cc2)S(=O)(=O)C)c3cc(F)c(F)c(F)c3)CC1)C(=O)Cc4ccc(cc4)S(=O)(=O)C\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H19N3O/c1-23-12-11-16-19(15-9-5-6-10-17(15)21-20(16)23)22-18(24)13-14-7-3-2-4-8-14/h2-10H,11-13H2,1H3,(H,21,22,24)\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][N][C][C][O][C][C][Ring1][=Branch1][=C][C][=C][Ring2][Ring1][=Branch1][Ring1][#C]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)NCC(O)COc1nccs1\\n\",\n        \"output\": \" -0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H12O2/c17-15-6-3-11(4-7-15)12-1-2-14-10-16(18)8-5-13(14)9-12/h1-10,17-18H\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][C][C][S][C][=C][C][=Ring1][Branch1][C][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)NC(=O)N2CCC(CC2)N3CCC(CC3)Oc4ccc(Cl)cc4C\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H18ClNO2S/c1-15-23(28-18-12-10-17(24)11-13-18)22-19(16-6-3-2-4-7-16)8-5-9-20(22)25(15)14-21(26)27/h2-13H,14H2,1H3,(H,26,27)\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-(di(propan-2-yl)amino)-2-phenyl-2-pyridin-2-ylbutanamide\\n\",\n        \"output\": \" -0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)CCC(=O)N1CCC(CC1)c2onc(n2)c3cccs3\\n\",\n        \"output\": \" -1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H16N2O2S/c16-12-15(11-2-1-7-18-11)9-13(17-12)8-14-5-3-10(13)4-6-14/h1-2,7,10H,3-6,8-9H2/t13-/m1/s1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CS(=O)(=O)c1ccc(C(=O)Nc2ccc(Cl)c(c2)c3ccccn3)c(Cl)c1\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-chloro-1h-indazol-3-amine\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" signature\\n\",\n        \"output\": \" signature is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [(2s,3s)-5-(2-dimethylaminoethyl)-2-(4-methoxyphenyl)-4-oxo-2,3-dihydro-1,5-benzothiazepin-3-yl] acetate\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H30N2O4S2/c29-22-10-9-21(25-24(22)28-26(31)34-25)23(30)17-27-12-4-15-33-16-14-32-13-11-19-7-3-6-18-5-1-2-8-20(18)19/h1-3,5-10,23,27,29-30H,4,11-17H2,(H,28,31)/t23-/m0/s1\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H18FN3O3S/c1-9(2)7-12(16)13-17-18-14(21-13)22(19,20)8-10-3-5-11(15)6-4-10/h3-6,9,12H,7-8,16H2,1-2H3/t12-/m0/s1\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-5-(oxan-4-yloxy)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[4-(2-tert-butylphenyl)sulfonylphenyl]-2,3,4-trihydroxy-5-[(2-propan-2-ylphenyl)methyl]benzamide\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (4r)-2-methyl-4-phenyl-3,4-dihydro-1h-isoquinolin-8-amine\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" nylon\\n\",\n        \"output\": \" nylon is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl 2-[4-[2-[[2-hydroxy-3-(phenoxy)propyl]amino]ethoxy]phenoxy]acetate\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1s,4s)-4-(3,4-dichlorophenyl)-n-methyl-1,2,3,4-tetrahydronaphthalen-1-amine\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nccc(n1)c2cccs2\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)/t11-/m0/s1\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H23N3O5/c1-5-13(15-10-9-11(2)29-15)22-16-17(20(27)19(16)26)23-14-8-6-7-12(18(14)25)21(28)24(3)4/h6-10,13,22-23,25H,5H2,1-4H3/t13-/m1/s1\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=N][N][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1][=C][Ring1][=C][C][=C][Ring2][Ring1][C][O][C]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H13BrN2O/c1-17-13-4-2-3-5-14(13)18(15(17)19)10-11-6-8-12(16)9-7-11/h2-9H,10H2,1H3\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc2nccc([C@H](O)C3CC4CCN3CC4C=C)c2c1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H22FN3O4/c1-10-8-22(6-5-21-10)16-14(20)7-12-15(18(16)27-2)23(11-3-4-11)9-13(17(12)24)19(25)26/h7,9-11,21H,3-6,8H2,1-2H3,(H,25,26)\\n\",\n        \"output\": \" -0.82\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][Ring2][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H17ClN2O4S2/c1-11-18(26-13-8-6-12(19)7-9-13)17-14(20-27(2,24)25)4-3-5-15(17)21(11)10-16(22)23/h3-9,20H,10H2,1-2H3,(H,22,23)\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(carbamoylamino)-5-[4-[(2-methoxyethylamino)methyl]phenyl]thiophene-3-carboxamide\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H18N2O3S/c20-16(13-23-14-5-2-1-3-6-14)18-8-10-19(11-9-18)17(21)15-7-4-12-22-15/h1-7,12H,8-11,13H2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C27H31F2N7O4/c1-3-36(9-10-37)8-5-11-40-23-15-21-18(14-22(23)39-2)27(31-16-30-21)33-24-12-17(34-35-24)13-25(38)32-20-7-4-6-19(28)26(20)29/h4,6-7,12,14-16,37H,3,5,8-11,13H2,1-2H3,(H,32,38)(H2,30,31,33,34,35)\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNC(=O)c1ccc(Nc2nccc(n2)c3cnc(C)n3C(C)C)cc1\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CNC(=O)c1ccc(Oc2ccc3CCN(CCc3c2)C4CCC4)nc1\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H10F2O2/c15-11-5-1-9(2-6-11)13(17)14(18)10-3-7-12(16)8-4-10/h1-8,13,17H\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-diethylamino-2-oxochromene-3-carboxylic acid\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][Branch1][=Branch1][C][Branch1][C][C][C][C][=N][N][=C][Branch1][C][N][S][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)c1c(O)c(O)c(C=O)c2c(O)c(c(C)cc12)c3c(C)cc4c(C(C)C)c(O)c(O)c(C=O)c4c3O\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][Branch1][C][Cl][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][#C]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(Cc1c[nH]c2ccccc12)C(=O)O\\n\",\n        \"output\": \" -1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][O][C][=C][C][=C][C][C][N][Branch1][=Branch2][C][C][C][Ring1][#Branch1][=C][Ring1][O][C][C][C][C][Ring1][Ring2][N][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H30N4O5/c1-30-19-2-3-21-20(13-19)28(24(29)16-33-21)9-8-27-6-4-17(5-7-27)25-14-18-12-22-23(15-26-18)32-11-10-31-22/h2-3,12-13,15,17,25H,4-11,14,16H2,1H3\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H19ClFN5O2/c21-13-1-2-14(15(22)9-13)20-18(16-3-6-23-11-24-16)19(25-26-20)12-4-7-27(8-5-12)17(29)10-28/h1-3,6,9,11-12,28H,4-5,7-8,10H2,(H,25,26)\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COCCCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cccc(Nc2ncnc3ccccc23)c1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC1CCN(CC1)c2nccc(C(=O)NCC34CC5CC(CC(C5)C3)C4)c2Cl\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccn2c(NC(=O)c3ccccc3)c(nc2c1)c4cccs4\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" [O-][n+]1cc(ccc1Cl)C(=O)Nc2ccc(F)cc2\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H14ClFN4O2S2/c1-7(5-22)18-12-11-13(21-15(23)25-11)20-14(19-12)24-6-8-3-2-4-9(16)10(8)17/h2-4,7,22H,5-6H2,1H3,(H2,18,19,20,21,23)/t7-/m1/s1\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(N)n(n1)c2ccccc2\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H8N2S/c10-9-11-8(6-12-9)7-4-2-1-3-5-7/h1-6H,(H2,10,11)\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-1-[(2r,4r,5r)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one\\n\",\n        \"output\": \" -1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(3,4-difluorophenyl)-4-[[(3s)-piperidin-3-yl]amino]thieno[2,3-d]pyridine-7-carboxamide\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" art\\n\",\n        \"output\": \" art is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(NC1CC1)c2cc(on2)c3cccs3\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H14FN5/c17-12-6-2-1-5-10(12)9-11-14(18)21-16(22-15(11)19)13-7-3-4-8-20-13/h1-8H,9H2,(H4,18,19,21,22)\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc2c(Nc3ccc(Br)cc3F)ncnc2cc1OC[C@@H]4CCCN(C)C4\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC[C@H]1CCCN1CCCOc2ccc3c(Nc4cc(CC(=O)Nc5cccc(F)c5F)[nH]n4)ncnc3c2\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@H](NC1=NC(=O)[C@](C)(S1)C(F)(F)F)c2ccccc2F\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H31ClN4O/c23-19-18(1-4-25-20(19)27-5-2-17(24)3-6-27)21(28)26-13-22-10-14-7-15(11-22)9-16(8-14)12-22/h1,4,14-17H,2-3,5-13,24H2,(H,26,28)\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H16N2O2/c22-18(21-14-15-8-3-1-4-9-15)17-12-7-13-20-19(17)23-16-10-5-2-6-11-16/h1-13H,14H2,(H,21,22)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-chloro-2-[[(3r,5s)-3,5-dimethyl-4-(2-phenylacetyl)piperazin-1-yl]methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n,5,6,6-tetramethylbicyclo[2.2.1]heptan-5-amine\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)Cc1ccc(cc1)[C@H](C)C(=O)NS(=O)(=O)C\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-n,n-dimethyl-2,2-di(phenyl)butanamide\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(COc1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16N2O2/c1-12-11-19(17(21)13-7-3-2-4-8-13)15-10-6-5-9-14(15)18-16(12)20/h2-10,12H,11H2,1H3,(H,18,20)\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=N][C][=C][Branch1][C][C][C][=C][Branch2][Ring1][S][C][=C][Ring1][#Branch1][N][Ring1][#Branch2][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C]\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NCc1nc2ccccc2[nH]1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H7IN2S/c10-6-2-1-3-7-5(6)4-8(13-7)9(11)12/h1-4H,(H3,11,12)\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[3,5-dimethyl-4-[3-(3-methyl-1,2-oxazol-5-yl)propoxy]phenyl]-5-(trifluoromethyl)-1,2,4-oxadiazole\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][C][C][C][C][C][C][C][C][=Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1(CCC(=O)N1Cc2cccs2)C(=O)NC3CCCCC3\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3c(cccc3n1CC(=O)O)c4ccccc4\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[4-[[4-(pyridin-4-ylmethyl)phenyl]sulfamoyl]phenyl]acetamide\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][=C][C][Branch2][Branch1][N][C][C][=Branch1][C][=O][N][C][C][C][C@@][Branch2][Ring1][O][C][C][N+1][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][Branch1][Branch1][C][C][Ring1][Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Branch1][Branch1][C][Ring2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring2][Ring2][#Branch1]\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 12h-indolo[2,1-b]quinazolin-6-one\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H18ClNO/c1-9(15-13(2,3)4)12(16)10-6-5-7-11(14)8-10/h5-9,15H,1-4H3\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccc(F)cc2)N)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1nnc2CN=C(c3ccccc3)c4cc(Cl)ccc4n12\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(CN2CCNCC2)cc1C(=O)NCC34CC5CC(CC(C5)C3)C4\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfanyl-2-methyl-4-pyrazin-2-ylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H12F4N2OS/c1-7(8-5-3-4-6-9(8)14)18-11-19-10(20)12(2,21-11)13(15,16)17/h3-7H,1-2H3,(H,18,19,20)/t7-,12+/m0/s1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-(4-chlorophenyl)-6-methyl-6h-1,3,5-triazine-2,4-diamine\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][C][=C][Branch2][Ring1][C][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H10O4/c1-12-9(11)6-13-8-4-2-7(10)3-5-8/h2-5,10H,6H2,1H3\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch1][#C][C][C][=C][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][=C][Ring1][#C][C][=Branch1][C][=O][N][C][C][C@@H1][Branch1][C][O][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-iodo-1-benzothiophene-2-carboximidamide\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-(4-fluorophenyl)-5-methylamino-6-oxopyrimidin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H28N2O/c25-22(23-15-10-18-24-16-8-3-9-17-24)21(19-11-4-1-5-12-19)20-13-6-2-7-14-20/h1-2,4-7,11-14,21H,3,8-10,15-18H2,(H,23,25)\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" bubble\\n\",\n        \"output\": \" bubble is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cccc(Nc2c(cnc3c(C)cc(cc23)S(=O)(=O)c4cccc(c4)C(=O)N(C)C)C(=O)N)c1\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(C)cc(c1)c2oc(SCC(=O)N3CCN(CC3)C(=O)c4occc4)nn2\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1=C(OCc2ccc(F)cc2)C(=O)C=CO1\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" women\\n\",\n        \"output\": \" women is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][P][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][C][C][C][Branch1][P][O][C][C][C][C][Branch1][C][C][Branch1][C][C][C][=Branch1][C][=O][O][=C][Ring1][P]\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H13Cl2NO2S/c1-10-17(23-12-7-5-11(18)6-8-12)13-3-2-4-14(19)16(13)20(10)9-15(21)22/h2-8H,9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H7N3S/c9-8-10-7(11-12-8)6-4-2-1-3-5-6/h1-5H,(H2,9,10,11)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][Branch2][=Branch1][C][C][N][C][=Branch1][C][=O][N][C][=C][Branch2][Ring2][P][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][S][=O][O][C]\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C@@H1][Branch1][C][C][C@H1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -1.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-nitrophenol\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[[6-[(2-cyclopentylacetyl)amino]indazol-1-yl]methyl]-3-methoxy-n-phenylsulfonylbenzamide\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][=N][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=C][Branch1][C][C][N][Ring1][=C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)(C)NC(=O)Nc1ccc(cc1)c2c(N)nc(N)nc2COCc3ccccc3\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Ring2][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Branch1][=C][N][C][=Branch1][C][=O][O][C][C][C][C][C][Ring1][Branch1][C][=C][Ring2][Ring1][C][Ring1][#C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C34H30N2O5/c1-23-29(36-33(41-23)26-12-6-3-7-13-26)20-21-40-27-18-16-24(17-19-27)22-31(34(38)39)35-30-15-9-8-14-28(30)32(37)25-10-4-2-5-11-25/h2-19,31,35H,20-22H2,1H3,(H,38,39)/t31-/m0/s1\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(2-chlorophenothiazin-10-yl)-n,n-dimethylpropan-1-amine\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nccc2ccccc12\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-chloro-1h-indazole\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1N(C2CCCC2)c3nc(Nc4ccc(cc4OC)C(=O)NC5CCN(C)CC5)ncc3N(C)C1=O\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12N2O3/c1-6(2)10(15)13-7-3-4-8-9(5-7)12(17)14-11(8)16/h3-6H,1-2H3,(H,13,15)(H,14,16,17)\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" beech\\n\",\n        \"output\": \" beech is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenoxy)-4-(ethylsulfonylamino)-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" -0.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H33N5O4/c1-30-8-3-9-32(11-10-30)24-17-21(35-2)16-22-25(33)18-23(29-26(22)24)27(34)28-19-4-6-20(7-5-19)31-12-14-36-15-13-31/h4-7,16-18H,3,8-15H2,1-2H3,(H,28,34)(H,29,33)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][=Branch2][N][C][=N][C][=C][C][N][=C][Branch2][Ring1][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][C][Ring1][N][=N][Ring1][S][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F][C][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCC(=O)NCC[C@@H]1CCc2ccc3OCCc3c12\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][N][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][Ring1][#Branch1][=N][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[2-[(1r)-1-[(4-chlorophenyl)sulfonyl-(2,5-difluorophenyl)amino]ethyl]-5-fluorophenyl]butanoic acid\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][N][=C][Branch2][Ring1][C][N][=C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][F][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][C][C][Branch1][C][O][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[[4-[(2,3-dimethylindazol-6-yl)-methylamino]pyrimidin-2-yl]amino]-2-methylbenzenesulfonamide\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C6H6N4/c7-5-4-1-2-8-6(4)10-3-9-5/h1-3H,(H3,7,8,9,10)\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][N][C][C][Branch1][=Branch2][N][C][C][O][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][Ring1][=Branch1][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][P][N][C][=Branch1][C][=O][C][=C][C][=C][C][C][C][N][Branch1][=N][C][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][Ring1][P][=Ring1][=N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc2c(c1)c(Sc3cccc(Cl)c3)c(C)n2CC(=O)O\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=S(=O)(Nc1cccnc1)c2ccccc2\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C7H5FN2/c8-6-2-1-5-4-9-10-7(5)3-6/h1-4H,(H,9,10)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][S][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=N][Ring1][O][C][Ring2][Ring1][N][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H21NO2/c1-12(2)17-10-14(18)11-19-16-9-5-7-13-6-3-4-8-15(13)16/h3-9,12,14,17-18H,10-11H2,1-2H3/t14-/m0/s1\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][N][=C][Branch2][Ring1][=Branch1][N][C][=C][C][=C][Branch1][O][O][C][C][N][C][C][C][C][Ring1][Branch1][C][=C][Ring1][=C][N][=C][Ring2][Ring1][Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][Branch1][C][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" mine\\n\",\n        \"output\": \" mine is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)NC[C@H](O)COc1cccc2ccccc12\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc2C(=O)N(C(=O)c2c1)c3ccccc3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNC(=O)C[C@H](Nc1ncc(Cl)c(Nc2cc([nH]n2)C3CC3)n1)c4ccc(F)cc4\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1(C)NC(=O)N(C1=O)c2ccc(c(c2)C(F)(F)F)[N+](=O)[O-]\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(C(=O)Cc2ccccc2)c(O)c1\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc2c(c1)c(CC(=O)O)c(C)n2c3ccnc4cc(Cl)ccc34\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" value\\n\",\n        \"output\": \" value is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nccc(n1)c2c[nH]c3ccccc23\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C@@H1][C][C][C@H1][Ring1][Branch1][C][C@H1][Branch1][Ring2][C][Ring1][#Branch1][O][C][=Branch1][C][=O][C][Branch1][Ring1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H13Cl2NO/c15-12-5-1-10(2-6-12)14(18,9-17)11-3-7-13(16)8-4-11/h1-8,18H,9,17H2\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H5N3O5/c8-7(11)4-1-5(9(12)13)3-6(2-4)10(14)15/h1-3H,(H2,8,11)\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-(cyclopropylmethoxy)-n-(3,5-dichloropyridin-4-yl)-4-(difluoromethoxy)benzamide\\n\",\n        \"output\": \" 3.95\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C][Branch1][Ring1][C][O][C][N][C][=Branch1][C][=O][C][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H21N3O/c1-2-25-20-6-4-3-5-18(20)19-15-17(8-9-21(19)25)24-22(26)10-7-16-11-13-23-14-12-16/h3-6,8-9,11-15H,2,7,10H2,1H3,(H,24,26)\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H29Cl2N3O4S/c1-17-2-5-21(6-3-17)34(31,32)27-24(30)29-12-8-19(9-13-29)28-14-10-20(11-15-28)33-23-7-4-18(25)16-22(23)26/h2-7,16,19-20H,8-15H2,1H3,(H,27,30)\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=N][C][Branch2][Ring1][N][N][C][=N][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][Branch1][C][C][C][=C][C][=C][Ring1][#Branch1][Cl][=C][C][=Branch1][Branch1][=N][Ring2][Ring1][#Branch1][N][C][C][N][Branch1][Ring2][C][C][O][C][C][Ring1][=Branch2]\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)COCCN1CCN(CC1)C(c2ccccc2)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1CC(CN)CC(CO)C1\\n\",\n        \"output\": \" -1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H15NO5/c1-15-9-4-2-3-5-10(9)16-6-8(13)7-17-11(12)14/h2-5,8,13H,6-7H2,1H3,(H2,12,14)\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfinyl-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][Cl][=N][C][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H28N4O3S/c30-21-9-8-20(24-23(21)29-25(32)33-24)22(31)16-27-13-10-17-4-6-18(7-5-17)15-26-14-11-19-3-1-2-12-28-19/h1-9,12,22,26-27,30-31H,10-11,13-16H2,(H,29,32)/t22-/m0/s1\\n\",\n        \"output\": \" -0.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2cc(Nc3cc(C)ccc3Cl)ncn2)cc1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1cccc(OCc2cnc(Cl)s2)c1\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-chloro-2-[(3-methyl-4-phenylsulfonylpiperazin-1-yl)methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[4-[5-(4-chloro-2-fluorophenyl)-4-pyrimidin-4-yl-2h-pyrazol-3-yl]piperidin-1-yl]-2-hydroxyethanone\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Branch1][Branch2][C][C][C][=Branch1][C][=O][C][C][=C][C][Ring1][O][=C][Ring1][#C]\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1-adamantylmethyl)-5-amino-2-chlorobenzamide\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H16N2O/c1-3-18-15-7-5-4-6-13(15)14-10-12(17-11(2)19)8-9-16(14)18/h4-10H,3H2,1-2H3,(H,17,19)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H24FNO4/c1-25-21-5-3-16(11-17(21)4-6-22(25)26)15-29-20-13-18(12-19(24)14-20)23(27-2)7-9-28-10-8-23/h3-6,11-14H,7-10,15H2,1-2H3\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H30O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12,16-19H,4-11H2,1-3H3/t16-,17+,18-,19-,20-,21+/m0/s1\\n\",\n        \"output\": \" 3.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][N][=C][N][=C][Ring1][P][C][=C][Ring2][Ring1][Branch1][O][C][C][C][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)N1CCC[C@H](CN2C(=Nc3ccc(cc3C2=O)c4ccc(Cl)cc4)C)C1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)Cc1ccccc1Sc2ccc(C)cc2N\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-methyl-8-pyridin-4-yl-2h-[1,2,4]triazolo[4,5-a]quinolin-1-one\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2nccc(C(O)C3CC4(CCN3CC4)C=C)c2c1\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch2][N][C][=N][C][=C][Branch1][C][Cl][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=C][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H30N6O3/c1-26(2,27)25(35)31-22(11-16-13-28-20-9-5-3-7-18(16)20)24(34)32-23(30-15-33)12-17-14-29-21-10-6-4-8-19(17)21/h3-10,13-15,22-23,28-29H,11-12,27H2,1-2H3,(H,30,33)(H,31,35)(H,32,34)/t22-,23-/m1/s1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-phenylmorpholine-4-carboxamide\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H23N3O2/c1-15-18(19-4-2-3-5-20(19)23-15)12-13-22-14-17-8-6-16(7-9-17)10-11-21(25)24-26/h2-11,22-23,26H,12-14H2,1H3,(H,24,25)/b11-10+\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-6-methyl-6-phenyl-3,5-dihydropyrimidin-4-one\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" pentyl n-[1-[(2r,3r,4s,5r)-3,4-dihydroxy-5-methyloxolan-2-yl]-5-fluoro-2-oxopyrimidin-4-yl]carbamate\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H12O4/c15-10-3-1-9(2-4-10)7-13(17)12-6-5-11(16)8-14(12)18/h1-6,8,15-16,18H,7H2\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(Nc2cc(Nc3ccc(OCC(O)CN(C)C)cc3)ncn2)cc1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2-methylphenyl)-(4-pyridin-2-ylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=S(=O)(Nc1cccnc1)c2cccs2\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][C][N][C][Branch1][Ring2][C][Ring1][=Branch1][=C][Branch2][Ring1][=C][C][=C][Branch1][#Branch2][C][=Branch1][C][=O][N][C][Ring1][=Branch1][=O][C][=C][N][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring2][Ring1][O][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H9NO2/c15-8-5-6-11-12(7-8)9-3-1-2-4-10(9)13(16)14(11)17/h1-7H,15H2\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[3-[(2s)-1-methoxypropan-2-yl]oxy-5-[(2s)-1-phenylpropan-2-yl]oxybenzoyl]amino]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(3,4-dichlorophenyl)methyl]-5-methoxyindole-2-carboxylic acid\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1c(c(CN2CCOCC2)nn1c3ccc(F)cc3)c4ccccc4\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-8-(4-methoxypyridin-3-yl)-n-propylcinnoline-3-carboxamide\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=N][C][S][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][C][N][C][Ring1][=N][=Ring1][=Branch2]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1cccc(C(=O)N2CCN(CC2)c3ccccn3)c1Cl\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H10N2/c1-5-3-6(2)9-7(8)4-5/h3-4H,1-2H3,(H2,8,9)\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1C(=O)c2cc(ccc2c3ccccc13)c4ccsc4\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H8N4/c1-2-4-8(5-3-1)6-7-9-10-12-13-11-9/h1-7H,(H,10,11,12,13)/b7-6+\\n\",\n        \"output\": \" -0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(2-chlorophenyl)-n-[(1r)-1-(3-methoxyphenyl)ethyl]propan-1-amine\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H10ClN3/c15-10-4-3-5-11(8-10)18-14-12-6-1-2-7-13(12)16-9-17-14/h1-9H,(H,16,17,18)\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][C][N][C][=N][C][Branch1][Branch1][S][C][C][C][=N][C][=C][Ring1][#Branch2][N][=N][N][Ring1][Branch1][C@@H1][C][C@H1][Branch1][Ring1][C][O][C@@H1][Branch1][C][O][C@H1][Ring1][Branch2][O]\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C@H1][Branch1][C][C][N][Ring2][Ring1][Ring2][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" salad\\n\",\n        \"output\": \" salad is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-hydroxy-2-(3-hydroxyphenyl)isoindole-1,3-dione\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch2][Ring1][Branch2][C@H1][C][C][C@@][Branch1][#Branch1][C][C][C][O][Ring1][Branch1][C][C@@H1][Ring1][#Branch2][N][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H26F3N3OS/c23-22(24,25)17-6-7-21-19(16-17)28(18-4-1-2-5-20(18)30-21)9-3-8-26-10-12-27(13-11-26)14-15-29/h1-2,4-7,16,29H,3,8-15H2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H23BrN2O3/c1-4-19-7-5-6-12(19)10-18-16(20)13-8-11(17)9-14(21-2)15(13)22-3/h8-9,12H,4-7,10H2,1-3H3,(H,18,20)/t12-/m0/s1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Oc1ccc(cc1)C2=CC(=O)c3ccccc3N2\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring2][Ring1][=C][C][=C][Ring1][=Branch1][C][N][C][=C][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H24F4N4O5/c1-15(2)21(22(36)26(28,29)30)33-20(35)13-34-23(17-8-10-18(27)11-9-17)31-12-19(24(34)37)32-25(38)39-14-16-6-4-3-5-7-16/h3-12,15,21H,13-14H2,1-2H3,(H,32,38)(H,33,35)\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCC(CC)CNC(=O)c1ccc2c(c1)c(Cc3ccc(cc3OC)C(=O)NS(=O)(=O)c4ccccc4C)cn2C\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H22N4O5S/c1-2-35(32,33)18-8-6-17(7-9-18)34-22-14-21-20(27-25(28-21)19-5-3-4-12-26-19)13-16(22)15-29-23(30)10-11-24(29)31/h3-9,12-14H,2,10-11,15H2,1H3,(H,27,28)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][C][C][C][Ring1][=Branch1][C][C][N][C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=C][Ring1][=Branch1][S+1][Branch1][C][C][O-1]\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H26ClN3O5S/c1-31(29,30)19-7-6-14(9-16(19)22)15(8-13-4-2-3-5-13)21(28)25-20-11-23-17(10-24-20)18(27)12-26/h6-7,9-11,13,15,18,26-27H,2-5,8,12H2,1H3,(H,24,25,28)/t15-,18-/m1/s1\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(3-chlorophenyl)amino]pyrido[4,3-c]quinoline-8-carboxylic acid\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][=C][C][Branch1][C][F][=C][Branch1][#Branch1][C][=C][Ring1][#C][Ring1][#Branch1][N][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][S][C][N][C][=C][N][Branch1][#Branch1][C][C][Branch1][C][C][C][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][Ring1][=N][=C][Ring1][S][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC1Nc2cc(Cl)c(cc2C(=O)N1c3ccccc3C)S(=O)(=O)N\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][Branch1][=Branch2][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H20N4OS/c1-2-21-11-15-12-22-19(25-15)14-9-7-13(8-10-14)18(24)23-17-6-4-3-5-16(17)20/h3-10,12,21H,2,11,20H2,1H3,(H,23,24)\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][NH1][N][=C][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][O][C][C][O][C][=Branch1][C][=O][C][Branch1][#Branch1][C][C][C][C][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@]1(CCCN1c2nc(Nc3cc([nH]n3)C4CC4)c5cccn5n2)C(=O)Nc6ccc(F)nc6\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-n-[2-chloro-4-(diethylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H26BrN7O2S/c24-18-15-27-22(30-20(18)25-9-5-10-26-21(32)19-8-4-13-34-19)28-16-6-3-7-17(14-16)29-23(33)31-11-1-2-12-31/h3-4,6-8,13-15H,1-2,5,9-12H2,(H,26,32)(H,29,33)(H2,25,27,28,30)\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][=C][C][C][C][N][Branch2][Ring2][C][C][C][C][Branch2][Ring1][Ring2][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][Ring2][Ring1][#Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1nccn1CC2CCc3c(C2=O)c4ccccc4n3C\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][N][Branch1][=Branch1][C][C][N][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nccc(n1)c2cc3C(=O)NC[C@H](CCF)c3[nH]2\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][Cl][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1c(I)cc(I)c2cccnc12\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C2=C(C=C1c3ccccc3)C(=O)N(CCN4CCOCC4)C(=O)N2)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H31N3O4/c1-18-15-19(2)25(20(3)16-18)26(31)30-23(27(32)33)17-21-8-10-22(11-9-21)34-14-6-13-29-24-7-4-5-12-28-24/h4-5,7-12,15-16,23H,6,13-14,17H2,1-3H3,(H,28,29)(H,30,31)(H,32,33)/t23-/m0/s1\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" postage\\n\",\n        \"output\": \" postage is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H23ClN2O5S/c1-15-12-22(9-10-23(15)29(26,27)18-5-3-2-4-6-18)13-16-11-17(21)7-8-19(16)28-14-20(24)25/h2-8,11,15H,9-10,12-14H2,1H3,(H,24,25)\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=N][C][=N][C][Branch2][Ring1][Branch1][O][C][=C][C][=C][Branch1][=Branch1][C][=C][Ring1][=Branch1][F][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H20N2/c1-3-7-15(8-4-1)13-17-11-12-18-14-16-9-5-2-6-10-16/h1-10,17-18H,11-14H2\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1(C)CNC(=O)c2sc(nc2C1)N3CCOCC3\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H](NC1=NC(=O)C(C)(S1)C(F)(F)F)c2ccccc2F\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.77\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][#Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)c2cc3ccccc3[nH]2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][NH1][C][=C][Branch1][Branch2][C][C][N][Branch1][C][C][C][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (4-methoxyphenyl)methyl 4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-methyl-3,5-di(thiophen-2-yl)-3h-pyrido[3,2-f][1,4]diazepin-2-amine\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H13F3N2O3/c19-18(20,21)10-4-3-5-11(8-10)22-15(24)9-13-12-6-1-2-7-14(12)23-16(13)17(25)26/h1-8,23H,9H2,(H,22,24)(H,25,26)\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H24N2O/c1-22-18-12-6-5-10-16(18)14-21-17-11-7-13-20-19(17)15-8-3-2-4-9-15/h2-6,8-10,12,17,19-21H,7,11,13-14H2,1H3/t17-,19-/m0/s1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)c1ccc(OC(=O)CCCCCN=C(N)N)cc1\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H26N2/c1-16(14-21(2)3)15-22-19-10-6-4-8-17(19)12-13-18-9-5-7-11-20(18)22/h4-11,16H,12-15H2,1-3H3\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s,3s)-n-[(2-methoxyphenyl)methyl]-2-phenylpiperidin-3-amine\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-[(3-cyclobutyl-1,2,4,5-tetrahydro-3-benzazepin-8-yl)oxy]-n-methylpyridine-3-carboxamide\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H17FN2O3/c21-13-5-6-16-12(7-13)9-18(22-16)20(26)23-17-8-11-3-1-2-4-14(11)15(17)10-19(24)25/h1-7,9,15,17,22H,8,10H2,(H,23,26)(H,24,25)/t15-,17-/m1/s1\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][C@H1][C][N][Branch1][Branch2][C][=Branch1][C][=O][O][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][F][=C][Ring1][#Branch1][N][C][=C][N][=C][Ring1][Branch1]\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H20F2N2O6/c1-13(12-31-2)32-18-5-15(22(28)27-21-4-3-14(11-26-21)23(29)30)6-19(10-18)33-20-8-16(24)7-17(25)9-20/h3-11,13H,12H2,1-2H3,(H,29,30)(H,26,27,28)/t13-/m0/s1\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2,3-difluorophenyl)-2-[5-[[7-[3-(2-hydroxyethyl-(2-methylpropyl)amino)propoxy]-6-methoxyquinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][#Branch2][C][N][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=N][C][=C][Branch1][=Branch1][N+1][=Branch1][C][=O][O-1][N][Ring1][Branch2][C][C][O]\\n\",\n        \"output\": \" -0.11\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H11NO5/c1-8-2-4-9(5-3-8)13(17)10-6-11(15(19)20)14(18)12(16)7-10/h2-7,16,18H,1H3\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cc(Oc2ccc3OCOc3c2)nc(Oc4ccc(cc4)n5ccnc5)n1\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2-(benzotriazol-2-yl)-4-methylphenoxy]acetic acid\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][=N][C][N][C][C][C][=C][C][=C][Branch1][#C][N][C][C@H1][Branch1][C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring1][S][C][=C][C][=C][Branch1][C][O][C][Branch1][Ring2][N][C][=O][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl]-(oxolan-2-yl)methanone\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[5-[[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-yl]amino]pyrimidin-2-yl]benzamide\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-chloro-2-cyclohexylphenoxy)acetic acid\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" horn\\n\",\n        \"output\": \" horn is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H26N4O5S/c1-14(2)11-28-24-21(22(31)27(3)25(28)33)20(23(32)29-12-16(30)13-34-29)19(35-24)10-15-8-9-26-18-7-5-4-6-17(15)18/h4-9,14,16,30H,10-13H2,1-3H3/t16-/m0/s1\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][O][S][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][C][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nc(N)nc(n1)c2ccc(Cl)cc2\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O[C@@H](CNCCCSCCNCCc1ccccc1Cl)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" ethiopia\\n\",\n        \"output\": \" ethiopia is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-dimethyl-2-[2-(phenylmethyl)phenoxy]ethanamine\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(2-methoxyphenyl)methyl]-2-methylbenzimidazole\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O[C@@H](CNCCCSCCOCCc1ccccc1)c2ccc(O)c3NC(=O)Sc23\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cn(C[C@H]2CN(C(=O)O2)c3ccc(C4=CCS(=O)(=O)CC4)c(F)c3)nn1\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" thieno[3,2-e]pyrimidin-4-amine\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C11H12N4O2/c12-10-7(11(13)15-14-10)3-6-1-2-8-9(4-6)17-5-16-8/h1-2,4H,3,5H2,(H5,12,13,14,15)\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NCC(O)(c1ccccc1)c2ccccc2\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H13N3O2/c16-15(17)9-5-6-11-10(8-9)13-12-4-2-1-3-7-14(11)12/h5-6,8H,1-4,7H2\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" ethernet\\n\",\n        \"output\": \" ethernet is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-[(e)-2-chloro-1,2-di(phenyl)ethenyl]phenoxy]-n,n-diethylethanamine\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" N(c1ccccc1)c2cc(Nc3ccccc3)[nH]n2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2cc(F)cc(F)c2)N)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H18F2N4O2S/c18-10-4-9(5-11(19)6-10)14-7-13(16(26-14)23-17(20)25)15(24)22-12-2-1-3-21-8-12/h4-7,12,21H,1-3,8H2,(H,22,24)(H3,20,23,25)/t12-/m0/s1\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(4-dimethylaminophenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-piperidin-1-ylethyl 3-methyl-4-oxo-2-phenylchromene-8-carboxylate\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][S][C][Branch2][Ring1][Ring2][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][=N][Ring1][S]\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" furan-2-yl-[4-(4-methylphenyl)sulfonylpiperazin-1-yl]methanone\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H21NO/c1-18(2)12-13-19-17-11-7-6-10-16(17)14-15-8-4-3-5-9-15/h3-11H,12-14H2,1-2H3\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][Branch1][N][C][Branch1][C][N][=N][C][Ring1][#Branch1][=N][Ring1][O][C][=C][Branch1][C][Br][C][=C][C][=C][Ring1][#Branch1][Br]\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][Branch1][#C][C][N][C][C][C][=C][C][=C][C][=C][Ring1][O][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H11ClN4O2/c1-19-10-3-2-8(13)6-9(10)16-12(18)17-11-7-14-4-5-15-11/h2-7H,1H3,(H2,15,16,17,18)\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-ethoxyphenyl)-6,7-dihydro-5h-pyrrolo[1,2-a]imidazole\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=N][C][=C][N][Ring1][Branch1][C][C][C][C][C][=C][Branch1][Branch1][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O][C]\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H17F2N5OS2/c1-16(2,7-24)23-13-11-12(20-14(19)26-11)21-15(22-13)25-6-8-4-3-5-9(17)10(8)18/h3-5,24H,6-7H2,1-2H3,(H3,19,20,21,22,23)\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H27ClN4O4/c1-30-20-12-16-18(13-21(20)31-11-5-10-29-8-3-2-4-9-29)26-14-27-24(16)28-22-17(25)6-7-19-23(22)33-15-32-19/h6-7,12-14H,2-5,8-11,15H2,1H3,(H,26,27,28)\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-aminophenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][F][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][C][N][Branch1][C][C][C][Branch1][O][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CN=C1c2ccccc2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccc(cc1)C2=Cc3cc(O)ccc3OC2=O\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H26O4/c1-14-15(2)22(26)20(16(3)21(14)25)18(17-10-6-4-7-11-17)12-8-5-9-13-19(23)24/h4,6-7,10-11,18H,5,8-9,12-13H2,1-3H3,(H,23,24)\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cn1cncc1c2c3C(=O)N(CC4CC4)C(=O)N(CC5CC5)c3nn2Cc6ccnc7ccc(Cl)cc67\\n\",\n        \"output\": \" 4.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H12F2N6O3S/c16-10-2-1-3-11(17)12(10)13(24)23-14(18)21-15(22-23)20-8-4-6-9(7-5-8)27(19,25)26/h1-7H,(H2,19,25,26)(H3,18,20,21,22)\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC[C@H]1N(C2CCCC2)c3nc(Nc4ccc(cc4OC)C(=O)NC5CCN(C)CC5)ncc3N(C)C1=O\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-fluoro-2-pyridin-4-ylquinoline-4-carboxylic acid\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=N][S][C][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6,7-dimethoxy-n-phenylquinazolin-4-amine\\n\",\n        \"output\": \" 3.04\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-fluoro-1,3-benzothiazol-2-amine\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cccc(c1)S(=O)(=O)c2c(C)n(CC(=O)O)c3ccc(C)cc23\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[3-(trifluoromethyl)phenyl]-4,5-dihydropyrazol-3-amine\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1=CC(=O)C2=C(O1)c3ccccc3N(C2=O)c4ccccc4\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" ethyl 4-aminobenzoate\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][P][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 6-hydroxy-8-[(1r)-1-hydroxy-2-[[1-(4-methoxyphenyl)-2-methylpropan-2-yl]amino]ethyl]-4h-1,4-benzoxazin-3-one\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1h-indol-2-yl-piperazin-1-ylmethanone\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][=N][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H18N6O2S/c20-28(26,27)16-8-6-14(7-9-16)12-13-21-17-10-11-18-22-23-19(25(18)24-17)15-4-2-1-3-5-15/h1-11H,12-13H2,(H,21,24)(H2,20,26,27)\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-(4-aminopiperidin-1-yl)-3-chloropyridine-4-carboxamide\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-hydroxy-6-phenylpyrano[3,2-c]quinoline-4,5-dione\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [(1r,5s)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2-hydroxy-2-phenylacetate\\n\",\n        \"output\": \" -1.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H27ClN2O4/c1-16-12-25(14-19-11-20(24)8-9-21(19)30-15-23(28)29)13-17(2)26(16)22(27)10-18-6-4-3-5-7-18/h3-9,11,16-17H,10,12-15H2,1-2H3,(H,28,29)/t16-,17+\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H14FN5O3/c1-10-6-15(25-19-10)13-3-2-11(7-14(13)17)22-9-12(24-16(22)23)8-21-5-4-18-20-21/h2-7,12H,8-9H2,1H3/t12-/m0/s1\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=C][C][=C][Ring2][Ring1][C][O][C]\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1CCC[C@H]1CNC(=O)c2c(O)c(Cl)cc(Cl)c2OC\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch2][N][C][=Branch1][C][=O][C][=C][C][=C][Ring1][O]\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-(1,8-diethyl-4,9-dihydro-3h-pyrano[3,4-b]indol-1-yl)acetic acid\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][N][C][=N][C][=Branch1][Branch1][=N][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H27N3O4/c1-16-9-11-19(26-24(29)17-7-6-8-20(13-17)28(2)3)15-21(16)27-25(30)18-10-12-22(31-4)23(14-18)32-5/h6-15H,1-5H3,(H,26,29)(H,27,30)\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H31N3O6S2/c1-11-15-14(12(2)26)18(27)25(15)16(19(28)30-10-31-20(29)22(3,4)5)17(11)33-13-8-24(9-13)21-23-6-7-32-21/h11-15,26H,6-10H2,1-5H3/t11-,12-,14-,15-/m1/s1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3c(Cl)cccc3n1CC(=O)O\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][N][Branch1][Branch1][C][C][C][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (4-methylphenyl) 1,4-diazabicyclo[3.2.2]nonane-4-carboxylate\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H19N3O/c1-2-13-3-9-18(10-4-13)23-20(24)17-8-6-14-11-16(19(21)22)7-5-15(14)12-17/h3-12H,2H2,1H3,(H3,21,22)(H,23,24)\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN[C@@H](C)C(=O)N[C@@H](C1CCCCC1)C(=O)N2CCC[C@H]2C(=O)N[C@@H](C(c3ccccc3)c4ccccc4)C(=O)OC\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H23ClFN5O3/c1-31-18-10-17-14(9-19(18)32-13-5-7-29(8-6-13)11-20(25)30)22(27-12-26-17)28-16-4-2-3-15(23)21(16)24/h2-4,9-10,12-13H,5-8,11H2,1H3,(H2,25,30)(H,26,27,28)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc2OCOc2c1Nc3ncnc4cc(OCCN5CCCC5)cc(OC6CCOCC6)c34\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1CCN(CC1)C(=O)c2cc3ccccc3[nH]2\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H12O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-6,13,16-18H,7H2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-(2-methyl-3-propan-2-ylimidazol-4-yl)-n-phenylpyrimidin-2-amine\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(2-bromophenyl)-1-(2-hydroxy-4-nitrophenyl)urea\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-methyl-2h-[1,2,4]triazolo[4,5-a]quinolin-1-one\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H21ClN2O/c21-17-7-5-16(6-8-17)20(24)9-11-23(12-10-20)14-15-13-22-19-4-2-1-3-18(15)19/h1-8,13,22,24H,9-12,14H2\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H17ClFNO2/c20-16-5-1-13(2-6-16)18(23)14-9-11-22(12-10-14)19(24)15-3-7-17(21)8-4-15/h1-8,14H,9-12H2\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H26F3N3O4S/c1-13-11-24(12-18(7-8-18)16(23)26)9-10-25(13)30(28,29)15-5-3-14(4-6-15)17(2,27)19(20,21)22/h3-6,13,27H,7-12H2,1-2H3,(H2,23,26)/t13-,17?/m1/s1\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nc(nc(N)c1Cc2ccccc2F)c3ccccn3\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-(2,5-dihydropyrrole-1-carbonyl)-3-methyl-1-(2-methylpropyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H23NO2/c1-4-7-13-8-5-6-9-15(13)18-11-14(17)10-16-12(2)3/h4-6,8-9,12,14,16-17H,1,7,10-11H2,2-3H3\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@H]1C[C@H]2[C@@H]3CC[C@](O)(C(=O)CO)[C@@]3(C)C[C@H](O)[C@@H]2[C@@]4(C)C=CC(=O)C=C14\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-[3-(propan-2-ylamino)propoxy]-3-prop-2-enylphenyl]acetamide\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@@H1][C][N][C@@H1][C@@H1][Branch1][Ring2][C][Ring1][=Branch1][O][C@][Branch2][Ring1][P][C][C][C@H1][C@@H1][C][C][=C][C][C@@H1][Branch1][C][O][C][C][C@][Ring1][#Branch1][Branch1][C][C][C@H1][Ring1][N][C][C][Ring1][#C][=C][Ring2][Ring1][Ring1][C][C@@H1][Ring2][Ring1][=Branch2][C]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)Nc1cc(sc1C(=O)N)c2ccccc2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCc1nc2c(C)cc(cc2n1Cc3ccc(cc3)c4ccccc4C(=O)O)c5nc6ccccc6n5C\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl]piperidin-1-yl]-2-phenylacetic acid\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCC1(CCCCN(C)C1)c2cccc(O)c2\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1cccc(c1)c2nc3ccc(O)cc3s2\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(=O)C[C@H]1[C@@H](Cc2ccccc12)NC(=O)c3cc4cc(F)ccc4[nH]3\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H25ClFN5O2/c1-28-5-7-29(8-6-28)9-10-31-21-12-16-19(13-20(21)30-2)25-14-26-22(16)27-15-3-4-18(24)17(23)11-15/h3-4,11-14H,5-10H2,1-2H3,(H,25,26,27)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][C][=C][Branch2][Ring1][Ring2][O][C][=C][Ring1][=Branch1][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H12N2O4S/c16-20(17,15-10-2-1-5-14-9-10)11-3-4-12-13(8-11)19-7-6-18-12/h1-5,8-9,15H,6-7H2\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" methyl 3-(benzoyloxy)-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14O2/c15-13-7-3-11(4-8-13)1-2-12-5-9-14(16)10-6-12/h3-10,15-16H,1-2H2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1,3-dioxoisoindol-5-yl)-2-methylpropanamide\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21NO/c21-19(14-20-12-10-18(19)11-13-20)17-8-6-16(7-9-17)15-4-2-1-3-5-15/h1-9,18,21H,10-14H2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=Branch1][C][=O][N][Branch1][O][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H22ClN3O2/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3/h8-9H,4-7,16H2,1-3H3,(H,17,19)\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch2][Branch1][Ring1][C][C][C][N][Branch2][Ring2][#Branch1][C][C][C@H1][Branch2][Ring1][Ring1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][Branch1][C][F][=C][C][Branch1][C][Cl][=C][Ring1][Branch2][C][C][Ring2][Ring1][O][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C14H12O3/c15-11-6-7-12(14(17)9-11)13(16)8-10-4-2-1-3-5-10/h1-7,9,15,17H,8H2\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" geese\\n\",\n        \"output\": \" geese is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch2][C][=C][C][Branch1][Branch2][C][C][N][C][C][Ring1][=Branch1][O][C][=C][C][=C][C][=C][Ring1][#C][Ring1][=Branch1][C][Branch1][C][O][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H19ClN4O4S/c21-16-9-12-8-13(24-19(12)30-16)18(28)23-14-7-11-3-1-2-4-15(11)25(20(14)29)10-17(27)22-5-6-26/h1-4,8-9,14,24,26H,5-7,10H2,(H,22,27)(H,23,28)\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][Branch1][N][C][C][C][C][N][Branch1][C][C][C][Ring1][Branch2][C][=C][C][=C][C][Branch1][C][O][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[2-[4-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethylamino)piperidin-1-yl]ethyl]-7-methoxyquinoxalin-2-one\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1C(=O)C=Cc2cnc(Nc3ccc(OC)c(OC)c3)nc12\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=C][Branch1][C][C][C][=N][N][=C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][N][Ring2][Ring1][=Branch1][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][=C][N][C][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][N][=C][Ring1][#C][N]\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][O][O][C][=C][C][=C][Branch1][S][O][C][C][=Branch1][C][=O][N][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=C][Ring1][P][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-amino-8-(2,4-dimethoxyphenyl)-7-fluoro-n-propylcinnoline-3-carboxamide\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][Branch2][Ring1][=Branch2][N][C][=Branch1][C][=O][C][O][C][Branch1][O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][F][=N][N][=Ring1][=N][=C][C][=C][Ring2][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-ethyl-4-methyl-3-[6-(4-methylpiperazin-1-yl)-4-oxoquinazolin-3-yl]benzamide\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NS(=O)(=O)c1ccc2NC(C3CC=CC3c2c1)c4cccc5ccccc45\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)Oc1cc(Oc2ccc(cc2)S(=O)(=O)C)cc(c1)C(=O)Nc3nccs3\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCC(=C)C(=O)c1ccc(OCC(=O)O)c(Cl)c1Cl\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H18N6/c1-13(2)7-10-8(14(3)4)12-9(11-7)15(5)6/h1-6H3\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C30H30O8/c1-11(2)19-15-7-13(5)21(27(35)23(15)17(9-31)25(33)29(19)37)22-14(6)8-16-20(12(3)4)30(38)26(34)18(10-32)24(16)28(22)36/h7-12,33-38H,1-6H3\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=N][NH1][C][Ring1][Branch1][=C][Ring1][=Branch2]\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2-aminophenyl)-4-[5-(ethylaminomethyl)-1,3-thiazol-2-yl]benzamide\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1nccc(n1)c2ccccc2\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc(cc1)C2=Cc3ccc(O)cc3OC2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][N][C][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(4-ethoxyphenyl)-6,7,8,9-tetrahydro-5h-imidazo[1,2-a]azepine\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(Nc1ccc(Nc2ccc(NC(=O)c3ccccc3)c4C(=O)c5ccccc5C(=O)c24)c6C(=O)c7ccccc7C(=O)c16)c8ccccc8\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H25ClN2O5S/c1-2-18-14-23(10-11-24(18)30(27,28)19-6-4-3-5-7-19)13-16-12-17(22)8-9-20(16)29-15-21(25)26/h3-9,12,18H,2,10-11,13-15H2,1H3,(H,25,26)/t18-/m0/s1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(CC(=O)NCc1ccccc1)C2CCCO2\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-amino-7-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrrolo[4,5-e]pyrimidine-5-carboxamide\\n\",\n        \"output\": \" -0.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-hydroxy-2-phenyl-4h-2,4,1-benzodiazaborinin-3-one\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][N][C@H1][C][C][C][N][=C][Branch1][C][N][S][C][=Ring1][=Branch1][C][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[1-(1-benzofuran-2-yl)ethyl]-7-chloro-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H16N4O/c1-9(2)16-13-11(18-3)8-15-12(17-13)10-6-4-5-7-14-10/h4-9H,1-3H3,(H,15,16,17)\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(5-tert-butyl-2-methylpyrazol-3-yl)-3-(4-chlorophenyl)urea\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H8O2/c1-5-2-3-6(8)7(9)4-5/h2-4,8-9H,1H3\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN(CCO)CCCOc1cc2ncnc(Nc3cc(CC(=O)Nc4cccc(F)c4F)[nH]n3)c2cc1OC\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-(2-diethylaminoethoxy)-3-methoxyphenyl]-n-methyl-4-[4-(trifluoromethyl)phenyl]benzamide\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H18ClN3O4S/c20-16-7-11-6-13(22-18(11)28-16)17(26)21-14-5-10-3-1-2-4-15(10)23(19(14)27)8-12(25)9-24/h1-4,6-7,12,14,22,24-25H,5,8-9H2,(H,21,26)/t12-,14?/m1/s1\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][C][C][N][C][C][=C][C][=N][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O][N][=Ring1][#C][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1-[[6-(4-ethylsulfonylphenoxy)-2-pyridin-2-yl-3h-benzimidazol-5-yl]methyl]pyrrolidine-2,5-dione\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(cc1)c2cc(ccc2OCC(=O)O)C(F)(F)F\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H13ClN2O3S/c1-2-7-12-10(14)13-17(15,16)9-5-3-8(11)4-6-9/h3-6H,2,7H2,1H3,(H2,12,13,14)\\n\",\n        \"output\": \" -0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H8Cl3N3O4S2/c9-3-1-4-6(2-5(3)19(12,15)16)20(17,18)14-8(13-4)7(10)11/h1-2,7-8,13-14H,(H2,12,15,16)\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCCC(CC)CNC(=O)c1ccc2c(c1)c(Cc3ccc(cc3OC)C(=O)NS(=O)(=O)c4ccccc4C)cn2C\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H15ClN6O/c1-7-4-17-9(8(2)11(7)22-3)5-21-6-18-10-12(15)19-14(16)20-13(10)21/h4,6H,5H2,1-3H3,(H2,16,19,20)\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [4-[(4-methoxypyridin-2-yl)amino]piperidin-1-yl]-phenylmethanone\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C32H39NO4/c1-31(2,30(35)36)25-17-15-24(16-18-25)29(34)14-9-21-33-22-19-28(20-23-33)32(37,26-10-5-3-6-11-26)27-12-7-4-8-13-27/h3-8,10-13,15-18,28-29,34,37H,9,14,19-23H2,1-2H3,(H,35,36)\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H14N4O4S/c1-19-11-7-10(14-12(15-11)20-2)16-21(17,18)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H,14,15,16)\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NNC(=O)c1ccncc1\\n\",\n        \"output\": \" -0.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[7-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=Branch1][#Branch2][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (3,4-dichlorophenyl)methylsulfanylmethanimidamide\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2z)-2-[[4-methoxy-3-(morpholin-4-ylmethyl)phenyl]methylidene]-3,4-dihydronaphthalen-1-one\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H13NO2/c1-8-5-13(15)16-12-7-11-9(6-10(8)12)3-2-4-14-11/h5-7,14H,2-4H2,1H3\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][O][C][C][Branch1][C][O][C][O][C][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" quinolin-6-amine\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][C][=C][Branch1][#Branch2][C][=Branch1][C][=O][C][=Branch1][C][=O][N][C][=C][Branch1][Branch2][O][C][C][=Branch1][C][=O][N][C][=C][C][=C][Ring1][O][N][Ring2][Ring1][Ring1][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H9N3OS2/c1-15-9-7(3-2-4-11-9)8(14)13-10-12-5-6-16-10/h2-6H,1H3,(H,12,13,14)\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" link\\n\",\n        \"output\": \" link is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)(C)C(=O)NCc1ccc(NC(=O)N2CCCC(O)(C2)c3ccc(Cl)c(Cl)c3)cc1\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H15NO3/c1-2-5-16(20)19-11-8-9-13-12-6-3-4-7-14(12)17(21)18(22)15(13)10-11/h3-4,6-10H,2,5H2,1H3,(H,19,20)\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H11N5/c12-10-7-6-9(11(13)14-10)16-15-8-4-2-1-3-5-8/h1-7H,(H4,12,13,14)\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(C1CCN(CCC(N2CCN(CC2)c3ccccc3)c4ccccc4)CC1)C(=O)Cc5ccc(cc5)S(=O)(=O)C\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCc1c(O)c(ccc1OCc2ccc(cc2)C(=O)O)C(=O)C\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H25Cl2N3O3/c1-27-19(26)23-8-9-24(15(13-23)12-22-6-2-3-7-22)18(25)11-14-4-5-16(20)17(21)10-14/h4-5,10,15H,2-3,6-9,11-13H2,1H3/t15-/m1/s1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][=Branch1][C][=C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch2][O][C][C][=Branch1][C][=O][O][C][Branch1][C][Cl][=C][Ring1][N][Cl]\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-hydroxy-n,n-dimethyl-3-[[2-[[(1r)-1-(5-methylfuran-2-yl)propyl]amino]-3,4-dioxo-1-cyclobutenyl]amino]benzamide\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN(C)C(=O)[C@H](Cc1ccccc1)NC(=O)c2cc3ccccc3[nH]2\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-pyrrolidin-1-ylsulfonylaniline\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1NC(=O)C(Cc2cccc(Oc3ccccc3)c2)S1\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN1CCC[C@H](CN2CCN(CC2)C(=O)Nc3ccc(Cl)c(Cl)c3)C1\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OCCNCc1cc(Br)ccc1OCc2ccc(Cl)cc2\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H22FN3O/c1-2-20(16-9-4-3-5-10-16)29-25(30)22-19-13-6-7-14-21(19)28-24(23(22)27)17-11-8-12-18(26)15-17/h3-15,20H,2,27H2,1H3,(H,29,30)/t20-/m0/s1\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" joseph\\n\",\n        \"output\": \" joseph is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][C][C@H1][Ring1][Branch1][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][Branch1][C][Cl][=C][C][Branch1][C][Cl][=C][Ring1][=Branch2][O][C]\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][C][C][=C][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][=Branch2][N][C][=N][C][=Branch1][C][=O][C@][Branch1][C][C][Branch1][Ring2][S][Ring1][#Branch1][C][Branch1][C][F][Branch1][C][F][F][C][=C][C][=C][C][=C][Ring1][=Branch1][F]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H20F4N4O3/c1-10(2)15(16(29)19(21,22)23)26-14(28)9-27-17(11-4-6-12(20)7-5-11)25-8-13(24-3)18(27)30/h4-8,10,15,24H,9H2,1-3H3,(H,26,28)\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H18ClNO2S/c1-15-23(28-19-10-8-18(24)9-11-19)20-13-17(16-5-3-2-4-6-16)7-12-21(20)25(15)14-22(26)27/h2-13H,14H2,1H3,(H,26,27)\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(5-chloro-1,3-benzodioxol-4-yl)-5-propan-2-yloxy-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2c(Nc3c(Cl)ccc4OCOc34)ncnc2cc1OCC5CCN(C)CC5\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][Ring1][=C][=O]\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(C)c2c(N)c(sc2n1)C(=O)NCc3ccccc3\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCCNc1nc(SCCC)nc2c1nnn2[C@@H]3C[C@H](CO)[C@@H](O)[C@H]3O\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccnc4ccc(F)cc34)c2C(=O)N5CC[C@@H](O)C5\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" church\\n\",\n        \"output\": \" church is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring1][#Branch2][C][N][C][C][C][S][C][C][O][C][C][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][S][C][Ring1][O][=Ring1][=Branch1]\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H11N3O4/c17-16(20)11-6-7-13(12(9-11)19(21)22)23-14-5-1-3-10-4-2-8-18-15(10)14/h1-9H,(H2,17,20)\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" stew\\n\",\n        \"output\": \" stew is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-tert-butyl-n-[6-(2-hydroxyethoxy)-5-(2-methoxyphenoxy)-2-pyrimidin-2-ylpyrimidin-4-yl]benzenesulfonamide\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1C=COc2cc(OCc3ccccc3)ccc12\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3CCOCC3)c(F)c2\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H27Cl2N3O3S2/c23-16-4-1-3-14(19(16)24)7-9-25-8-2-11-31-12-10-26-13-18(29)15-5-6-17(28)20-21(15)32-22(30)27-20/h1,3-6,18,25-26,28-29H,2,7-13H2,(H,27,30)/t18-/m0/s1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(2-fluorophenyl)phenanthrene-9,10-dione\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[2-fluoro-5-[(e)-3-(3-hydroxy-2-methoxycarbonylphenoxy)prop-1-enyl]phenyl]-1,2-oxazole-3-carboxylic acid\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1,3-benzodioxol-4-yl)-7-methoxy-5-(1-methylpiperidin-4-yl)oxyquinazolin-4-amine\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H18Cl2N2O2/c14-5-7-17(8-6-15)11-3-1-10(2-4-11)9-12(16)13(18)19/h1-4,12H,5-9,16H2,(H,18,19)\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H13N3O2/c1-21-14(12-5-3-2-4-6-12)11-15-16(18(21)22)17(20-23-15)13-7-9-19-10-8-13/h2-11H,1H3\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][O][O][C][C][Branch1][C][F][Branch1][C][F][F][C][=C][N][=C][Ring1][N][C][S+1][Branch1][C][O-1][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(N1NC(=O)C2=C(C1=O)C(=O)c3ccc(Cl)cc3N2)c4ccsc4\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC\\\\C(=C(/c1ccccc1)\\\\c2ccc(\\\\C=C\\\\C(=O)O)cc2)\\\\c3ccccc3\\n\",\n        \"output\": \" 3.89\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(4-fluorobenzoyl)-n-(phenylmethyl)piperidine-1-carboxamide\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C31H42N6O3/c1-30(2,32)28(39)34-26(18-23-20-33-25-15-10-9-14-24(23)25)27(38)37-17-11-16-31(21-37,29(40)36(5)35(3)4)19-22-12-7-6-8-13-22/h6-10,12-15,20,26,33H,11,16-19,21,32H2,1-5H3,(H,34,39)/t26-,31-/m1/s1\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H13FN2O2/c19-13-8-10-14(11-9-13)21-17(22)16-7-4-12-20-18(16)23-15-5-2-1-3-6-15/h1-12H,(H,21,22)\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-amino-1-cyclopropyl-7-[(3s,5r)-3,5-dimethylpiperazin-1-yl]-6,8-difluoro-4-oxoquinoline-3-carboxylic acid\\n\",\n        \"output\": \" -0.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)Nc1sc(cc1C(=O)N[C@H]2CCCNC2)c3cc(F)cc(F)c3\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H26F3N3O6/c1-16(2)24(25(37)28(29,30)31)33-23(36)15-34-21(18-8-4-3-5-9-18)12-11-20(26(34)38)32-22(35)14-17-7-6-10-19(13-17)27(39)40/h3-13,16,24H,14-15H2,1-2H3,(H,32,35)(H,33,36)(H,39,40)\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][C][=C][Branch2][Ring2][=C][N][=C][Branch1][=Branch1][C][Branch1][C][C][C][C][Branch2][Ring1][C][\\\\C][=C][\\\\C@@H1][Branch1][C][O][C][C@@H1][Branch1][C][O][C][C][=Branch1][C][=O][O][=C][Ring2][Ring1][Ring2][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][Branch1][C][C][C]\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][=C][C][=Branch1][#C][=N][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][O][Ring1][#Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=Branch1][C][C][C][Ring1][Ring2][C][=Branch1][C][=O][N][C][O][C][=Branch1][Branch1][=N][N][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H9F2N3O/c13-6-3-4-7(14)10-9(6)11(15)17-12(16-10)8-2-1-5-18-8/h1-5,12,16H,(H2,15,17)\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring2][Branch2][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=Branch1][Ring2][=N][Ring1][Branch1][C][=C][Branch1][C][C][N][=C][C][=C][C][Branch1][C][Br][=C][N][Ring1][O][Ring1][#Branch1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H21N3O2/c1-23(2)20(25)18(12-14-8-4-3-5-9-14)22-19(24)17-13-15-10-6-7-11-16(15)21-17/h3-11,13,18,21H,12H2,1-2H3,(H,22,24)/t18-/m0/s1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch2][Ring2][#C][C][=N][C][=C][C][=C][Ring1][=Branch1][C][N][C][=N][C][Branch2][Ring1][C][N][C][=C][C][=C][N][C][=Branch1][C][=O][C][C][Ring1][=Branch1][=C][Ring1][#Branch2][=N][C][=C][Ring1][P][C][Branch1][C][F][Branch1][C][F][F][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H29N5O5/c1-32-18-3-5-20-19(12-18)29(23(31)15-34-20)11-10-28-8-6-16(7-9-28)25-13-17-2-4-21-24(26-17)27-22(30)14-33-21/h2-5,12,16,25H,6-11,13-15H2,1H3,(H,26,27,30)\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H16N2O/c1-2-17(14-11-7-4-8-12-14)15(18)16-13-9-5-3-6-10-13/h3-12H,2H2,1H3,(H,16,18)\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][=N][N][C][=Branch1][C][=O][N][Ring1][=Branch1][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][=C][Ring1][=Branch1][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C24H29Cl2N3O4S/c1-17-4-2-3-5-23(17)34(31,32)27-24(30)29-12-8-18(9-13-29)28-14-10-19(11-15-28)33-20-6-7-21(25)22(26)16-20/h2-7,16,18-19H,8-15H2,1H3,(H,27,30)\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COCCOCCOc1ccc(cc1)c2cc(C(=O)N)c(NC(=O)N)s2\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[(3-chloro-2-fluorophenyl)methylsulfanyl]-7-[[(2r)-1-hydroxypropan-2-yl]amino]-3h-[1,3]thiazolo[5,4-e]pyrimidin-2-one\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=N][Ring1][#C][N][=C][N][=C][Ring2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch2][O][C][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H27Cl2N3O3S2/c23-16-4-1-3-14(19(16)24)7-9-25-10-12-31-11-2-8-26-13-18(29)15-5-6-17(28)20-21(15)32-22(30)27-20/h1,3-6,18,25-26,28-29H,2,7-13H2,(H,27,30)/t18-/m0/s1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(phenoxy)phenyl]propanoic acid\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][N][C][=Branch1][C][=O][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][C][O][C][=N][C][Branch1][C][N][=C][N][C][=Branch1][C][=O][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=N][=N][Ring2][Ring1][C]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)N1CCN(CC(O)COc2ccc(Br)cc2)CC1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H23NO/c20-17(16-4-2-1-3-5-16)19-12-18-9-13-6-14(10-18)8-15(7-13)11-18/h1-5,13-15H,6-12H2,(H,19,20)\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H18N2O6/c1-9-13(16(20)24-3)15(14(10(2)18-9)17(21)25-4)11-7-5-6-8-12(11)19(22)23/h5-8,15,18H,1-4H3\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H17FN2O2/c1-12-6-7-18-16(10-12)20(13(2)24(18)11-19(25)26)14-8-9-23-21-15(14)4-3-5-17(21)22/h3-10H,11H2,1-2H3,(H,25,26)\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)N4CCOCC4)ncc2F\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][S][C][=N][C][=C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=Ring1][S][N]\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-amino-n-pyridin-2-ylbenzenesulfonamide\\n\",\n        \"output\": \" -0.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][S][C][=N][C][=N][C][Branch1][=C][S][C][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=C][Ring1][#C][C][=Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)c2cc(nn2c3ccc(cc3)S(=O)(=O)N)C(F)(F)F\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-n-[2-chloro-4-(2-morpholin-4-ylethylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Branch2][N][C][Ring1][#Branch1][=C][Ring1][O][C][=Branch1][C][=O][N][N][Branch1][#Branch2][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Ring1][P][=O]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H7NO4/c16-13-10-4-2-1-3-9(10)12-7-8(15(18)19)5-6-11(12)14(13)17/h1-7H\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-chloro-1,1-dioxo-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][O][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][Cl][C][=Branch1][Ring2][=C][Ring1][#Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][C][C][=C][N][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N]\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1nc(N)nc2c1ncn2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O\\n\",\n        \"output\": \" -0.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC1C2CN(CC12)c3nc4N(C=C(C(=O)O)C(=O)c4cc3F)c5ccc(F)cc5F\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H15ClN4O3/c1-2-14(10-5-7-21-8-6-10)24-19(27)15-16(18(26)23-24)22-13-9-11(20)3-4-12(13)17(15)25/h3-9,14H,2H2,1H3,(H,22,25)(H,23,26)\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][N][C][C][N][Branch1][=N][C][C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring1][#C]\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-[4-(4-methylpiperazin-1-yl)-6-[(5-methyl-1h-pyrazol-3-yl)amino]pyrimidin-2-yl]sulfanylphenyl]cyclopropanecarboxamide\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][Branch1][Branch2][C][C][C][=Branch1][C][=O][O][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][P][Ring1][#Branch1]\\n\",\n        \"output\": \" -0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(Oc2ccc(Nc3ncnc4[nH]nc(OCCN5CCC(O)CC5)c34)cc2Cl)cn1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n'-[2-amino-6-[4-(trifluoromethyl)phenyl]pyrimidin-4-yl]-2-(4-fluorophenyl)quinoline-4,6-diamine\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring2][#Branch2][O][C][C][Branch2][Ring1][Branch2][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][N][C][=Branch1][C][=O][C][C][C][C][Ring1][#Branch1][=O][C][=C][Ring2][Ring1][S]\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2nc(Nc3ccc(cc3)N4CCN(CC4)C(=O)CO)ncc2F\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[5-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-3h-imidazol-4-yl]pyridine\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C9H7ClN2S/c10-7-3-1-6(2-4-7)8-5-13-9(11)12-8/h1-5H,(H2,11,12)\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl 3-[(7-chloro-1,4,10-trioxo-3,5-dihydropyridazino[4,5-b]quinolin-2-yl)methyl]benzoate\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc(cc1)S(=O)(=O)N2N=Cc3ccccc3B2O\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H25N5O3/c1-5-6-7-24-15(23-16-18(20)21-11-22-19(16)24)10-12-8-13(25-2)17(27-4)14(9-12)26-3/h8-9,11H,5-7,10H2,1-4H3,(H2,20,21,22)\\n\",\n        \"output\": \" 2.39\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][C][=C][N][Branch1][S][C][C][=C][C][=C][Branch1][C][F][C][Branch1][C][F][=C][Ring1][Branch2][C][=Branch1][C][=O][C][=C][Ring1][S]\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CC(O)COc1ccc(Nc2ncc(Cl)c(Nc3ccccc3)n2)cc1\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1cc(cc(F)c1C2=CCN(CC2)C=O)N3C[C@H](COc4ccon4)OC3=O\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H8ClFN2O2/c13-11-6-1-8(7-16(11)18)12(17)15-10-4-2-9(14)3-5-10/h1-7H,(H,15,17)\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[2-[(2r)-2-hydroxy-3-propylaminopropoxy]phenyl]-3-phenylpropan-1-one\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(1,8-dimethylimidazo[2,1-c]quinoxalin-4-yl)ethane-1,2-diamine\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Ring1][#Branch2][=C][Ring1][=C]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-(9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-ylmethyl)benzamide\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H14N2O2/c1-10-6-5-9-12(14(16)18)13(10)17-15(19)11-7-3-2-4-8-11/h2-9H,1H3,(H2,16,18)(H,17,19)\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][C][C@H1][C@@H1][C][C][C@][Branch1][C][O][Branch1][#Branch1][C][=Branch1][C][=O][C][O][C@@][Ring1][#Branch2][Branch1][C][C][C][C@H1][Branch1][C][O][C@@H1][Ring1][S][C@@][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2]\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][N][Branch1][C][C][C][=Ring1][=Branch1][C][Ring1][N][=O]\\n\",\n        \"output\": \" -0.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H18N3S/c1-18(2)11-5-7-13-15(9-11)20-16-10-12(19(3)4)6-8-14(16)17-13/h5-10H,1-4H3/q+1\\n\",\n        \"output\": \" -0.88\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C20H15F3N4O3/c21-8-1-2-15(13(22)3-8)27-7-12(20(29)30)17(28)9-4-14(23)19(25-18(9)27)26-5-10-11(6-26)16(10)24/h1-4,7,10-11,16H,5-6,24H2,(H,29,30)\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][Ring1][O][C][=C][C][=Branch1][Ring2][=C][Ring1][Branch2][C][=C][C][=C][Branch1][S][N][C][=Branch1][C][=O][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][Ring2][Ring1][C][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][#C][O][C][=C][Branch1][O][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][=Branch1][C][=O][O][C][C][N][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(cc1Cl)C(=O)Nc2ccc(Cl)nc2\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,3-benzothiazol-2-amine\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch1][N][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][S][Ring1][=N][=Branch1][C][=O][=O][C][=C][Ring2][Ring1][Ring1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC1=CC(=O)C2=C(O1)c3ccccc3N(Cc4ccccc4)C2=O\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCc1c(C)[nH]c2CCC(CN3CCOCC3)C(=O)c12\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1nnc(NS(=O)(=O)c2ccc(N)cc2)s1\\n\",\n        \"output\": \" -1.33\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[2-[(2s)-3-(5-fluorospiro[3h-1-benzofuran-2,4'-piperidine]-1'-yl)-2-hydroxypropoxy]-4-hydroxyphenyl]acetamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H20N4O3S/c1-20(2)7-8-23-11-5-3-10(4-6-11)13-9-12(14(17)21)15(24-13)19-16(18)22/h3-6,9H,7-8H2,1-2H3,(H2,17,21)(H3,18,19,22)\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][Branch1][N][C][=N][C][=C][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N][C][=C][Ring2][Ring1][Ring2]\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H27NO2/c1-13-3-4-17(23-2)8-18(13)21-19(22)12-20-9-14-5-15(10-20)7-16(6-14)11-20/h3-4,8,14-16H,5-7,9-12H2,1-2H3,(H,21,22)\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][C][N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][N][=C][C][=C][C][=N][N][Ring1][=Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" c1ccc(cc1)c2ccc3ccccc3n2\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOc1cc(CC(=O)N[C@@H](CC(C)C)c2ccccc2N3CCCCC3)ccc1C(=O)O\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][C][O][N][=C][Branch1][Ring2][N][=Ring1][Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" -1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3c(NS(=O)(=O)C)cccc3n1CC(=O)O\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H15NO/c1-8(11-2)10(12)9-6-4-3-5-7-9/h3-8,10-12H,1-2H3/t8-,10-/m0/s1\\n\",\n        \"output\": \" -1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H5F3N2OS/c9-8(10,11)14-4-1-2-5-6(3-4)15-7(12)13-5/h1-3H,(H2,12,13)\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-(4-chlorophenyl)-2-methyl-3,4-dihydro-1h-isoquinoline\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" celeste\\n\",\n        \"output\": \" celeste is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" circle\\n\",\n        \"output\": \" circle is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 7-[(1r)-2-[2-[3-[2-(4-ethylphenyl)ethylamino]propylsulfanyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-(azetidine-1-carbonyl)-1-(2-methylpropyl)-6-[[2-(trifluoromethyl)phenyl]methyl]thieno[3,2-e]pyrimidine-2,4-dione\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H19N5/c1-12(2)22-13(3)19-11-16(22)15-9-10-18-17(21-15)20-14-7-5-4-6-8-14/h4-12H,1-3H3,(H,18,20,21)\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" wine\\n\",\n        \"output\": \" wine is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" [2-(carbamoyloxymethyl)-2-methylpentyl] n-propan-2-ylcarbamate\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-hydroxyphenyl)isoindole-1,3-dione\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H24ClN5O4/c1-23(2,15-3-5-16(24)6-4-15)21(31)26-22-28-27-20(33-22)19(30)25-17-7-9-18(10-8-17)29-11-13-32-14-12-29/h3-10H,11-14H2,1-2H3,(H,25,30)(H,26,28,31)\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CS(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(CCC(c3ccccc3)c4ccccc4)CC2)cc1\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" summer\\n\",\n        \"output\": \" summer is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=N][C][Branch1][Branch2][S][C][C][=Branch1][C][=O][N][=N][Ring1][N]\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCN1CCCC1CNC(=O)c2cc(ccc2OC)S(=O)(=O)N\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-2-methyl-3-phosphonooxypropanoic acid\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H14O6/c1-21-13-4-3-9(5-14(13)22-2)11-8-23-15-7-10(18)6-12(19)16(15)17(11)20/h3-8,18-19H,1-2H3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H23ClN2O3/c1-16(18-7-9-20(10-8-18)25(30)31)27-24(29)22-4-2-3-19-13-14-28(23(19)22)15-17-5-11-21(26)12-6-17/h2-12,16H,13-15H2,1H3,(H,27,29)(H,30,31)/t16-/m0/s1\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-[3-[2,6-dichloro-4-(4,5-dihydro-1,3-oxazol-2-yl)phenoxy]propyl]-3-methyl-1,2-oxazole\\n\",\n        \"output\": \" 3.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C9H10N4O2S2/c1-6-11-12-9(16-6)13-17(14,15)8-4-2-7(10)3-5-8/h2-5H,10H2,1H3,(H,12,13)\\n\",\n        \"output\": \" -1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H10N2/c1-2-6-11(7-3-1)12-10-15-9-5-4-8-13(15)14-12/h1-10H\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" NC(=O)C1CCCCC1\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1C(=O)C(=Cc2cnc(NC(CCO)CCO)nc12)Oc3ccc(F)cc3F\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)c(Cl)c3)c2cc1NC(=O)\\\\C=C\\\\CN4CCCCC4\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(2-diethylaminoethyl)-5-[(z)-(5-fluoro-2-oxo-1h-indol-3-ylidene)methyl]-2,4-dimethyl-1h-pyrrole-3-carboxamide\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(CN1CCCCC1)(C(=O)c2ccccc2)c3ccccc3\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Fc1ccc(Nc2oc(nn2)C(=O)Nc3ccc(nc3)N4CCOCC4)cc1F\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H25ClN2O4/c1-16-13-24(9-10-25(16)21(26)11-17-5-3-2-4-6-17)14-18-12-19(23)7-8-20(18)29-15-22(27)28/h2-8,12,16H,9-11,13-15H2,1H3,(H,27,28)/t16-/m0/s1\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][=Branch2][N][C][C][N][C][C][Ring1][=Branch1][C][=C][C][=C][C][=C][C][=C][N][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H13ClN4/c1-11-20-21-16-10-19-17(12-5-3-2-4-6-12)14-9-13(18)7-8-15(14)22(11)16/h2-9H,10H2,1H3\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C8H8N2O/c1-11-8-4-2-3-7-6(8)5-9-10-7/h2-5H,1H3,(H,9,10)\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1CCc2c(NC(=O)Cc3ccccc3)c4ccccc4nc12\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][=N][S][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccccc1CN2CCc3sccc3C2\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2,4-dihydroxy-5-propan-2-ylphenyl)-[5-[(4-methylpiperazin-1-yl)methyl]-1,3-dihydroisoindol-2-yl]methanone\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)N1C(=O)N(C)C(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CCS(=O)(=O)C4\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-dimethyl-2-(1-phenyl-1-pyridin-2-ylethoxy)ethanamine\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-[[5-amino-1-(2,6-difluorobenzoyl)-1,2,4-triazol-3-yl]amino]benzenesulfonamide\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H14FN3O3/c1-3-22-15(21)13-12-7-18(2)14(20)10-6-9(16)4-5-11(10)19(12)8-17-13/h4-6,8H,3,7H2,1-2H3\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc(cc1)S(=O)(=O)Nc2nccs2\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n,n-diethyl-4-[piperidin-4-ylidene-[3-(trifluoromethyl)phenyl]methyl]benzamide\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][=C][=C][Branch1][C][C][N][Ring1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][C][=N][C][=C][C][=Branch1][Branch2][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H17ClN2O4/c20-12-5-6-14-17(7-8-21-18(14)9-12)22-16-4-2-1-3-15(16)19(25)26-11-13(24)10-23/h1-9,13,23-24H,10-11H2,(H,21,22)\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H23NO/c1-13-6-8-15(9-7-13)16(18)14(2)12-17-10-4-3-5-11-17/h6-9,14H,3-5,10-12H2,1-2H3\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ccnc(n1)c2cccnc2\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" OC1(CCN(CCCC(=O)c2ccc(F)cc2)CC1)c3ccc(Cl)cc3\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H23ClN2O5S/c21-18-6-7-19(28-14-20(24)25)17(12-18)13-22-8-10-23(11-9-22)29(26,27)15-16-4-2-1-3-5-16/h1-7,12H,8-11,13-15H2,(H,24,25)\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)C1=CN(C2CC2)c3cc(N4CCNCC4)c(F)cc3C1=O\\n\",\n        \"output\": \" -0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][N][C][=Branch1][C][=O][C][N][Branch2][Ring1][Ring1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][=C][=C][Ring2][Ring1][C][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(OCc4ccccn4)c(C)c3)c2cc1OC\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nccc(n1)n2ccc3ccccc23\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" rooster\\n\",\n        \"output\": \" rooster is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C30H39FN4O4/c1-19-18-33-27(23-12-13-23)30(38)35(3)20(2)28(36)34-25(17-21-10-14-24(31)15-11-21)29(37)32-16-6-8-22-7-4-5-9-26(22)39-19/h4-5,7,9-11,14-15,19-20,23,25,27,33H,6,8,12-13,16-18H2,1-3H3,(H,32,37)(H,34,36)/t19-,20-,25-,27+/m1/s1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H9N3/c1-2-6-10-9(5-1)14-12(15-10)11-7-3-4-8-13-11/h1-8H,(H,14,15)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][Branch1][C][C][=C][C][Branch1][C][N][=C][Branch1][Branch2][S][C][Ring1][=Branch1][=N][Ring1][O][C][=Branch1][C][=O][N][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (4,6-dimethylpyrimidin-5-yl)-[4-[(3s)-4-[(1r)-2-methoxy-1-[4-(trifluoromethyl)phenyl]ethyl]-3-methylpiperazin-1-yl]-4-methylpiperidin-1-yl]methanone\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" part\\n\",\n        \"output\": \" part is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C32H40N2O5S2/c1-4-34(32(35)24-25-10-14-29(15-11-25)40(2,36)37)28-18-21-33(22-19-28)23-20-31(26-8-6-5-7-9-26)27-12-16-30(17-13-27)41(3,38)39/h5-17,28,31H,4,18-24H2,1-3H3\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H17F2N3O2S/c18-13-6-5-12(9-14(13)19)22-8-7-20-16(17(22)24)25-10-15(23)21-11-3-1-2-4-11/h5-9,11H,1-4,10H2,(H,21,23)\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=N][C][=N][C][N][=C][NH1][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" subway\\n\",\n        \"output\": \" subway is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1N=Nc2c(ncn2C1=O)C(=O)N\\n\",\n        \"output\": \" -1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][C][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C22H20O4/c23-22(24)14-11-17-9-12-19(13-10-17)25-16-18-5-4-8-21(15-18)26-20-6-2-1-3-7-20/h1-10,12-13,15H,11,14,16H2,(H,23,24)\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][O][C][Branch1][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1]\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [4-[4-[c-(4-bromophenyl)-n-ethoxycarbonimidoyl]piperidin-1-yl]-4-methylpiperidin-1-yl]-(3,5-dichloropyridin-4-yl)methanone\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(1-methyl-3,6-dihydro-2h-pyridin-4-yl)phenol\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][=Branch1][C][=O][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-fluorophenyl)imidazo[1,2-a]pyridine\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[2-[[3-(1-adamantylmethylcarbamoyl)-4-chlorophenyl]amino]ethylamino]acetic acid\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][C][Branch1][C][O][Branch1][N][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" taxicab\\n\",\n        \"output\": \" taxicab is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H26N2O3/c1-2-3-4-5-6-7-8-9-10-14(19)17-13-11-12-15(20)18-16(13)21/h2,13H,1,3-12H2,(H,17,19)(H,18,20,21)/t13-/m0/s1\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCc1c(OCCCSc2ccc(CC(=O)O)cc2Cl)ccc3c(CC)noc13\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)(C)NC(=O)Nc1cccc(CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3)c1\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(9-methylsulfonylcarbazol-3-yl)-3-pyridin-4-ylpropanamide\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-bromobenzamide\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)N)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C26H35N7O2S/c1-19-18-27-25(29-20-9-11-22(12-10-20)33-15-13-32(5)14-16-33)30-24(19)28-21-7-6-8-23(17-21)36(34,35)31-26(2,3)4/h6-12,17-18,31H,13-16H2,1-5H3,(H2,27,28,29,30)\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Oc1ccc(CCc2ccc(O)cc2)cc1\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][Branch1][C][C][N][C][=Branch2][Ring1][#C][=C][Branch1][P][C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N+1][=Branch1][C][=O][O-1][C][=Branch1][C][=O][O][C][C][Branch1][C][C][C][C]\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" organisation\\n\",\n        \"output\": \" organisation is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-2-[(2-bromo-6-methylbenzoyl)amino]-3-[4-[(2,6-dichlorobenzoyl)amino]phenyl]propanoic acid\\n\",\n        \"output\": \" -0.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C1CC2(CCN1)OC(c3ccccc3)c4ccccc24\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C)CCOC(c1ccccc1)c2ccccc2C\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)(C)NC(=O)[C@@H]1CN(Cc2cccnc2)CCN1C[C@@H](O)C[C@@H](Cc3ccccc3)C(=O)N[C@@H]4[C@H](O)Cc5ccccc45\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC1(C)Cc2c(c3ccccc3)c(c(CC(=O)O)n2C1)c4ccc(Cl)cc4\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1CCCCCN1\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H8F2O3/c14-8-2-3-9(11(15)6-8)7-1-4-12(16)10(5-7)13(17)18/h1-6,16H,(H,17,18)\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H15NO/c1-2-4-14-12(3-1)9-15(17-14)13-10-16-7-5-11(13)6-8-16/h1-4,9-11H,5-8H2\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][C][C][=Branch1][C][=O][C][=C][Branch1][C][O][C][=C][Branch1][C][O][C][=C][Ring1][Branch2][O][Ring1][=N]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfanyl-2-methyl-5-methylsulfonylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C@@H1][Branch1][=C][N][C][C][C][S][C][=C][C][=Ring1][Branch1][C][Ring1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 3.69\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" azepan-2-one\\n\",\n        \"output\": \" -0.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccsc1CN2NC(=O)C3=C(C2=O)C(=O)c4ccc(Cl)cc4N3\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][#Branch1][C][N][C][C][C][=C][Branch1][Ring2][C][Ring1][=Branch1][NH1][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring2][O][C]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H10ClN3O2S2/c15-11-6-8-12(9-7-11)22(19,20)18-14-17-16-13(21-14)10-4-2-1-3-5-10/h1-9H,(H,17,18)\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H25F3N2O3S2/c1-13(2)12-27-20-17(19(29)26(3)21(27)30)18(31-10-6-9-28)16(32-20)11-14-7-4-5-8-15(14)22(23,24)25/h4-5,7-8,13,28H,6,9-12H2,1-3H3\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(1-benzothiophen-2-ylmethyl)-7-chloro-3,5-dihydropyridazino[4,5-b]quinoline-1,4,10-trione\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(Nc2ccnc(NCc3onc(c3)C4CC4)n2)n[nH]1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H30ClN3O4S/c1-18-2-8-23(9-3-18)33(30,31)26-24(29)28-14-10-20(11-15-28)27-16-12-22(13-17-27)32-21-6-4-19(25)5-7-21/h2-9,20,22H,10-17H2,1H3,(H,26,29)\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][O]\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-methoxy-1,3-benzothiazol-2-yl)benzamide\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][C][N][Branch2][Ring2][Ring1][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][O][N][=C][Branch1][Ring2][C][=Ring1][Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1][C][C][Ring2][Ring1][N]\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nnc(Cc2ccc(Cl)cc2)s1\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" cyclopentyl n-[1-[[2-methoxy-4-(phenylsulfonylcarbamoyl)phenyl]methyl]indol-6-yl]carbamate\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ncnc2ccccc12\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" australia\\n\",\n        \"output\": \" australia is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H24N4O/c1-16-13-17(15-27-11-4-12-27)14-25-22(16)18-7-9-19(10-8-18)23(28)26-21-6-3-2-5-20(21)24/h2-3,5-10,13-14H,4,11-12,15,24H2,1H3,(H,26,28)\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" propan-2-yl 7-[(2,6-difluorophenyl)methyl]-3-[(methyl-(phenylmethyl)amino)methyl]-2-[4-(2-methylpropanoylamino)phenyl]-4-oxothieno[3,2-e]pyridine-5-carboxylate\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][C][=N][C][=C][Branch1][C][N][N][=C][C][=C][C][=C][C][Ring1][=Branch1][=C][Ring1][O][S][Ring1][=C]\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H26Cl2F3N3O4S/c25-21-5-4-19(15-22(21)26)36-18-8-12-31(13-9-18)17-6-10-32(11-7-17)23(33)30-37(34,35)20-3-1-2-16(14-20)24(27,28)29/h1-5,14-15,17-18H,6-13H2,(H,30,33)\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(Cc1ccc(cc1)N(CCCl)CCCl)C(=O)O\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-phenylsulfanylquinoline\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C(Nc1ccc(nc1)N2CCOCC2)c3oc(Nc4ccccc4)nn3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-chloro-1-(4-fluorophenyl)-3-piperidin-4-ylindole\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14F3N3O2S/c1-10-13(20-7-6-14(10)24-9-16(17,18)19)8-25(23)15-21-11-4-2-3-5-12(11)22-15/h2-7H,8-9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][F][C][=C][C][Branch1][C][F][=C][Ring1][N][Ring1][Branch2][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2,3-difluorophenyl)-2-[5-[[7-[3-(2-hydroxyethyl-propylamino)propoxy]quinazolin-4-yl]amino]-2h-pyrazol-3-yl]acetamide\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H17ClN4O3S/c1-22(2)13-8-4-7-12-11(13)6-5-9-14(12)26(23,24)21-16-17(25-3)20-15(18)10-19-16/h4-10H,1-3H3,(H,19,21)\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" myanmar\\n\",\n        \"output\": \" myanmar is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-pyridin-2-ylacetamide\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H20N2S/c1-18(2)12-7-13-19-14-8-3-5-10-16(14)20-17-11-6-4-9-15(17)19/h3-6,8-11H,7,12-13H2,1-2H3\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C[C@@H]1NC(C)(C)CO[C@@]1(O)c2cccc(Cl)c2\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(5-bromo-3-methoxypyrazin-2-yl)-5-chlorothiophene-2-sulfonamide\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H27FN4O4/c1-13-20(10-18-17-9-15(24)3-4-19(17)27-22(18)30)26-14(2)21(13)23(31)25-11-16(29)12-28-5-7-32-8-6-28/h3-4,9-10,16,26,29H,5-8,11-12H2,1-2H3,(H,25,31)(H,27,30)/b18-10-/t16-/m0/s1\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C30H40N2O4/c1-19(31-17-28(35)25-5-6-27(34)26(13-25)18-33)7-20-3-2-4-21(8-20)12-29(36)32-30-14-22-9-23(15-30)11-24(10-22)16-30/h2-6,8,13,19,22-24,28,31,33-35H,7,9-12,14-18H2,1H3,(H,32,36)/t19-,22?,23?,24?,28+,30?/m1/s1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H17F3N4O3S/c1-8(2)12(13(25)16(17,18)19)22-11(24)7-23-14(10-4-3-5-27-10)21-6-9(20)15(23)26/h3-6,8,12H,7,20H2,1-2H3,(H,22,24)\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN(CC)CCNC(=O)c1cc(ccc1OC)S(=O)(=O)C\\n\",\n        \"output\": \" -0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-n-[1-(3-hydroxypropyl)-2-oxo-3,4-dihydroquinolin-3-yl]-6h-thieno[3,2-d]pyrrole-5-carboxamide\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3,4-dichlorophenyl)-4-[[(3s)-1-ethylpiperidin-3-yl]methyl]piperazine-1-carboxamide\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C32H47N5O5S/c1-8-42-32(39)37-14-12-36(13-15-37)31(38)28(17-23-10-9-11-24(16-23)30(33)34)35-43(40,41)29-26(21(4)5)18-25(20(2)3)19-27(29)22(6)7/h9-11,16,18-22,28,35H,8,12-15,17H2,1-7H3,(H3,33,34)/t28-/m0/s1\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Cc3ccccc3C(F)(F)F)c2C(=O)N4CC=CC4\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H9NO2S/c15-9-3-1-2-8(6-9)13-14-11-5-4-10(16)7-12(11)17-13/h1-7,15-16H\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C22H24Cl2N2O4/c1-15-12-25(13-17-11-19(24)5-6-20(17)30-14-22(28)29)7-8-26(15)21(27)10-16-3-2-4-18(23)9-16/h2-6,9,11,15H,7-8,10,12-14H2,1H3,(H,28,29)/t15-/m0/s1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" mail\\n\",\n        \"output\": \" mail is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C1NCCc2c1sc3ccccc23\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][Branch1][C][F][=C][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=N][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2cc(C)c3nnc(SCC(=O)N4CCN(CC4)C(=O)c5occc5)n3c2c1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[5-acetamido-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COCc1c(nc(C(C)C)c(\\\\C=C\\\\[C@@H](O)C[C@@H](O)CC(=O)O)c1c2ccc(F)cc2)C(C)C\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1c(C)cnc(Cn2cnc3c(Cl)nc(N)nc23)c1C\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][C][Branch1][C][F][=C][C][=C][Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=N][C][Branch1][#Branch2][N][C][C][C][C][C][O][Ring1][Branch1][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][P][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18F2N4O3/c1-25-17-11(10-22-19(24-17)23-13-4-6-27-7-5-13)8-16(18(25)26)28-15-3-2-12(20)9-14(15)21/h2-3,8-10,13H,4-7H2,1H3,(H,22,23,24)\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(4-aminophenyl)-3-ethylpiperidine-2,6-dione\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H12ClN5/c1-6-14-9(12)15-10(13)16(6)8-4-2-7(11)3-5-8/h2-6H,1H3,(H4,12,13,14,15)\\n\",\n        \"output\": \" -0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[e]pyrimidin-4-yl]piperazin-1-yl]-3-(propan-2-ylamino)propan-1-one\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][P]\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" difference\\n\",\n        \"output\": \" difference is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-n-(2-methylphenyl)sulfonylpiperidine-1-carboxamide\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][=C][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Ring1][=Branch2][C]\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)N)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=N][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Brc1ccc(OC(=O)N2CCN3CCC2CC3)cc1\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC[C@H](C)C(=O)O[C@H]1C[C@H](O)C=C2C=C[C@H](C)[C@H](CC[C@@H](O)C[C@@H](O)CC(=O)O)[C@@H]12\\n\",\n        \"output\": \" -0.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][C][Branch1][C][Br][=C][Branch1][C][N][C][=C][Ring1][Branch2][O][C]\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C@@H1][Branch2][Ring2][N][C][N][C][C][C][C][C][C][C][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][O][C][N][C][=Branch1][C][=O][C][=C][C][Ring1][N][=Ring1][#Branch1]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCn1c2ccccc2c3cc(NC(=O)N4CCOCC4)ccc13\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][N][=C][NH1][C][=Ring1][Branch1][C][Ring1][O][=O]\\n\",\n        \"output\": \" -0.09\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCc1ccc(CCOc2ccc(CC3SC(=O)NC3=O)cc2)nc1\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][C]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=C][C][=C][C][C][=Branch1][C][=O][N][Branch1][=N][C][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Ring2][Ring1][Ring1][=Ring1][#C]\\n\",\n        \"output\": \" 3.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch2][Ring1][O][C][O][C][=Branch1][C][=O][N][C][C][C][Branch1][O][C][N][C][=N][C][=C][C][=N][Ring1][=Branch1][C][C][Ring1][=C][C][=C][Ring2][Ring1][Branch2]\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" armenian\\n\",\n        \"output\": \" armenian is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][Branch1][S][C][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][=Branch1][C][=O][N][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=C][C][=C][Branch1][#C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][N+1][=Branch1][C][=O][O-1]\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cccc(COCC(O)CN2CCC(CC2)C(=O)N)c1\\n\",\n        \"output\": \" -0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" plantation\\n\",\n        \"output\": \" plantation is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H10ClN3O3S/c17-8-3-4-10-11(6-8)18-13-12(14(10)21)16(23)20(19-15(13)22)7-9-2-1-5-24-9/h1-6H,7H2,(H,18,21)(H,19,22)\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][=C][N][C@@H1][C][N][C][C][C][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][Branch1][Ring2][S][Ring1][Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" phenylmethyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-pyridin-3-ylpyridin-3-yl]carbamate\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@@H1][C][C@H1][C@@H1][C][C][C][=C][C][=Branch1][C][=O][C][=C][C@][Ring1][#Branch1][Branch1][C][C][C@@][Ring1][N][Branch1][C][F][C@@H1][Branch1][C][O][C][C@][Ring2][Ring1][C][Branch1][C][C][C@@][Ring2][Ring1][=Branch1][Branch1][C][O][C][=Branch1][C][=O][C][O]\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-butyl-1,2-di(phenyl)pyrazolidine-3,5-dione\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H18ClNS/c1-20(2)11-5-7-14-15-6-3-4-8-17(15)21-18-10-9-13(19)12-16(14)18/h3-4,6-10,12H,5,11H2,1-2H3/b14-7+\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][N][=C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Ring1][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][C][N][C][C][=C][C][Branch1][C][Cl][=C][C][=C][C][=N][C][Ring1][=Branch1][=C][Ring1][O][O]\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (7s)-2-(2-aminopyrimidin-4-yl)-7-(2-fluoroethyl)-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-2-[[4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl]methyl-methylamino]propanamide\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" garlic\\n\",\n        \"output\": \" garlic is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][O][C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=C][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" beast\\n\",\n        \"output\": \" beast is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H24FN9O/c1-23(21(34)26-15-7-8-18(24)25-13-15)9-3-10-32(23)22-28-20(17-4-2-11-33(17)31-22)27-19-12-16(29-30-19)14-5-6-14/h2,4,7-8,11-14H,3,5-6,9-10H2,1H3,(H,26,34)(H2,27,28,29,30,31)/t23-/m0/s1\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)CN1C(=O)N(C)C(=O)c2c1sc(Oc3cccc4ccccc34)c2C(=O)N5CC[C@@H](O)C5\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNC1=Nc2ncccc2C(=NC1c3cccs3)c4cccs4\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H20N2OS/c1-18-14-12(8-5-9-15-14)13(17)16-10-11-6-3-2-4-7-11/h5,8-9,11H,2-4,6-7,10H2,1H3,(H,16,17)\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC1=CC(=O)Nc2sc(C(=O)c3ccc(Br)cc3)c(N)c12\\n\",\n        \"output\": \" 2.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=C][Branch1][=Branch2][N][C][C][C][C][C][Ring1][=Branch1][C][S][C][=C][C][C][C][C][C][=Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][Branch2][Ring1][Ring1][C][=Branch1][C][=O][O][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][N][Ring1][#Branch1][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" tree\\n\",\n        \"output\": \" tree is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H20N4O2S/c1-13-4-8-16(9-5-13)23-14(2)21-22-19(23)26-12-18(24)20-15-6-10-17(25-3)11-7-15/h4-11H,12H2,1-3H3,(H,20,24)\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (r)-[(4r,5r,7s)-5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl]-(6-methoxyquinolin-4-yl)methanol\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C41H76N2O15/c1-15-29-41(10,49)34(45)24(4)31(42-53-21-52-17-16-50-13)22(2)19-39(8,48)36(58-38-32(44)28(43(11)12)18-23(3)54-38)25(5)33(26(6)37(47)56-29)57-30-20-40(9,51-14)35(46)27(7)55-30/h22-30,32-36,38,44-46,48-49H,15-21H2,1-14H3/b42-31+/t22-,23-,24+,25+,26-,27+,28+,29-,30+,32-,33+,34-,35+,36-,38+,39-,40-,41-/m1/s1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H12N2O3S/c1-17-10-5-7-11(8-6-10)18(15,16)14-12-4-2-3-9-13-12/h2-9H,1H3,(H,13,14)\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][N][=C][C][=C][Branch2][Ring1][Branch1][C][Branch1][C][O][C][C][C][Branch1][#Branch2][C][C][N][Ring1][=Branch1][C][C][Ring1][=Branch1][C][=C][C][Ring2][Ring1][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H14N4OS/c1-18-17-15(13-7-4-10-23-13)20-14(12-6-3-9-22-12)11-5-2-8-19-16(11)21-17/h2-10,15H,1H3,(H,18,19,21)\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C12H9F3N2O2/c1-7-10(6-16-19-7)11(18)17-9-4-2-8(3-5-9)12(13,14)15/h2-6H,1H3,(H,17,18)\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H12N2O2S/c1-19-11-8-5-9-12-13(11)16-15(20-12)17-14(18)10-6-3-2-4-7-10/h2-9H,1H3,(H,16,17,18)\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C66H103N17O16S/c1-9-35(6)52(69)66-81-48(32-100-66)63(97)76-43(26-34(4)5)59(93)74-42(22-23-50(85)86)58(92)83-53(36(7)10-2)64(98)75-40-20-15-16-25-71-55(89)46(29-49(68)84)78-62(96)47(30-51(87)88)79-61(95)45(28-39-31-70-33-72-39)77-60(94)44(27-38-18-13-12-14-19-38)80-65(99)54(37(8)11-3)82-57(91)41(21-17-24-67)73-56(40)90/h12-14,18-19,31,33-37,40-48,52-54H,9-11,15-17,20-30,32,67,69H2,1-8H3,(H2,68,84)(H,70,72)(H,71,89)(H,73,90)(H,74,93)(H,75,98)(H,76,97)(H,77,94)(H,78,96)(H,79,95)(H,80,99)(H,82,91)(H,83,92)(H,85,86)(H,87,88)/t35-,36-,37-,40-,41+,42+,43-,44+,45-,46-,47+,48-,52-,53-,54-/m0/s1\\n\",\n        \"output\": \" -0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H12O2S/c1-11-7-9-13(10-8-11)16(14,15)12-5-3-2-4-6-12/h2-10H,1H3\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H16N4O/c1-21(13-8-4-3-5-9-13)17-15(22-2)12-19-16(20-17)14-10-6-7-11-18-14/h3-12H,1-2H3\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Nc1cccc(C(=O)NCC23CC4CC(CC(C4)C2)C3)c1Cl\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(1h-benzimidazol-2-yl)-2-(4-methoxyphenyl)acetamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)Oc1cc(OCCN2CCN(CC2)C(=O)C)cc3ncnc(Nc4c(F)ccc5OCOc45)c13\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-(phenylmethyl)-1,2,3,4-tetrahydroisoquinoline\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 4-oxochromene-3-carboxylate\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-chloro-5-[(4-methylphenyl)methyl]-2,3-dihydro-1,5-benzothiazepin-4-one\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-methyl-n-(phenylmethyl)pyridin-2-amine\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15N5/c1-3-7-13(8-4-1)11-20(15-16-18-19-17-15)12-14-9-5-2-6-10-14/h1-10H,11-12H2,(H,16,17,18,19)\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" methyl 4-[(9,10-dioxophenanthren-3-yl)amino]-4-oxobutanoate\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-phenylpyrimidin-4-amine\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)c3ccc(F)cc3\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C4H6N2S/c1-6-3-2-5-4(6)7/h2-3H,1H3,(H,5,7)\\n\",\n        \"output\": \" -0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C29H35F2N7O4/c1-18(2)16-38(9-10-39)8-5-11-42-25-15-23-20(14-24(25)41-3)29(33-17-32-23)35-26-12-19(36-37-26)13-27(40)34-22-7-4-6-21(30)28(22)31/h4,6-7,12,14-15,17-18,39H,5,8-11,13,16H2,1-3H3,(H,34,40)(H2,32,33,35,36,37)\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" century\\n\",\n        \"output\": \" century is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H29Cl2N3O5S/c1-33-22-4-2-3-5-23(22)35(31,32)27-24(30)29-12-8-17(9-13-29)28-14-10-18(11-15-28)34-19-6-7-20(25)21(26)16-19/h2-7,16-18H,8-15H2,1H3,(H,27,30)\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-pyridin-2-ylbenzamide\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-fluoro-n-methyl-4-[[4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]benzamide\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[(3,4-difluorophenyl)amino]-n-(6-morpholin-4-ylpyridin-3-yl)-1,3,4-oxadiazole-2-carboxamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2,3-dihydroxy-6-methyl-7-(phenylmethyl)-4-propylnaphthalene-1-carboxylic acid\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C27H26N4O5S/c1-16-11-21(37(34,35)20-10-5-7-17(12-20)27(33)31(2)3)14-22-24(16)29-15-23(26(28)32)25(22)30-18-8-6-9-19(13-18)36-4/h5-15H,1-4H3,(H2,28,32)(H,29,30)\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cc(NC(=O)c2ccc(Cl)cc2)n(n1)c3ccccc3\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-[2-[(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl]imidazole\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncc(C(=O)N)c(Nc3ccc(F)c(Cl)c3)c2cc1OC\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H37N3O5S/c1-22(2)21-26(30-28(33)31-16-18-36-19-17-31)27(32)29-24(14-13-23-9-5-3-6-10-23)15-20-37(34,35)25-11-7-4-8-12-25/h3-12,15,20,22,24,26H,13-14,16-19,21H2,1-2H3,(H,29,32)(H,30,33)/b20-15+/t24-,26-/m0/s1\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H11NO2/c17-11-7-5-10(6-8-11)14-9-15(18)12-3-1-2-4-13(12)16-14/h1-9,17H,(H,16,18)\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" ethyl 1-(furan-2-ylmethyl)-5-hydroxy-2-methylindole-3-carboxylate\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][Ring2][C][C][=Branch1][C][=O][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-phenylsulfinyltetrazolo[5,1-f]pyridazine\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[1-(3-methoxybenzoyl)piperidin-4-yl]-1h-benzimidazol-2-one\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H19N3O4S/c1-26(23,24)21-16-5-3-2-4-14(16)15-12-13(6-7-17(15)21)19-18(22)20-8-10-25-11-9-20/h2-7,12H,8-11H2,1H3,(H,19,22)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][F][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][N][C][Branch1][C][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[4-chloro-3-(4-chlorophenyl)sulfanyl-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[4-[(3,4-dichloro-5-methyl1h-pyrrole-2-carbonyl)amino]piperidin-1-yl]-1,3-thiazole-5-carboxylic acid\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[2-(6-methylpyridin-2-yl)-5,6-dihydro-4h-pyrrolo[2,1-e]pyrazol-3-yl]quinoline-6-carboxamide\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(cc1S(=O)(=O)n2ccc(n2)c3c(C)nc4ccc(Br)cn34)[N+](=O)[O-]\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[2-[(2-fluorophenyl)methyl]tetrazol-5-yl]benzoic acid\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4cc(Cl)ccc34\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Fc1ccc(CC2=NNC(=O)c3ccccc23)cc1N4C(=O)CCC4=O\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2-amino-5-chlorophenyl)-(3,4,5-trimethoxyphenyl)methanone\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H16N2O/c1-12-17-14-8-4-5-9-15(14)18(12)11-13-7-3-6-10-16(13)19-2/h3-10H,11H2,1-2H3\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COC(=O)COc1ccc(cn1)C(=O)Nc2ccc(F)cc2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc2NC(=O)CN(C(c3ccccc3)c2c1)C(=O)c4ccccc4\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H17N3OS/c1-10-8-11(2)20-17-13(10)14(18)15(22-17)16(21)19-9-12-6-4-3-5-7-12/h3-8H,9,18H2,1-2H3,(H,19,21)\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H20N6O/c24-19-5-1-2-6-21(19)28-22(30)17-9-7-16(8-10-17)14-27-23-26-13-11-20(29-23)18-4-3-12-25-15-18/h1-13,15H,14,24H2,(H,28,30)(H,26,27,29)\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[4-methyl-3-[[2-[(1-methylpiperidin-3-yl)methoxy]pyrimidin-4-yl]amino]phenyl]-2-morpholin-4-ylpyridine-4-carboxamide\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H21N5O4S/c1-2-3-4-24-14-17-11(15)8-12(18-14)19(6-16-8)13-10(22)9(21)7(5-20)23-13/h6-7,9-10,13,20-22H,2-5H2,1H3,(H2,15,17,18)/t7-,9-,10-,13-/m1/s1\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H23ClN2O/c19-16-2-1-14(20)6-15(16)17(22)21-10-18-7-11-3-12(8-18)5-13(4-11)9-18/h1-2,6,11-13H,3-5,7-10,20H2,(H,21,22)\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" vase\\n\",\n        \"output\": \" vase is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(piperidin-2-ylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" ethyl 7-methyl-2-phenylimidazo[3,2-a]pyridine-3-carboxylate\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCNC(=O)CSc1ccc(cn1)S(=O)(=O)N2CCCC2\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H13F3N2O4S/c1-14(22,15(16,17)18)13(21)20-10-2-4-11(5-3-10)25(23,24)12-6-8-19-9-7-12/h2-9,22H,1H3,(H,20,21)\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C1CCC(CC1)NC2CCCCC2\\n\",\n        \"output\": \" -0.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H17N3O/c1-10-9-17(7-6-15-10)14(18)13-8-11-4-2-3-5-12(11)16-13/h2-5,8,10,15-16H,6-7,9H2,1H3\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3,4-dihydro-1h-isoquinolin-2-yl-[1-(5-pyrrol-1-yl-1,3,4-thiadiazol-2-yl)piperidin-4-yl]methanone\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-[[3-(2-methylpropoxy)-5-propan-2-yloxybenzoyl]amino]pyridine-3-carboxylic acid\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(OC)cc(c1)c2cc3cnc(N)nc3nc2N\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H23NO5/c1-29-21(26)11-5-3-2-4-10-20(25)24-15-12-13-18-19(14-15)16-8-6-7-9-17(16)22(27)23(18)28/h6-9,12-14H,2-5,10-11H2,1H3,(H,24,25)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][=C][Branch1][N][NH1][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][C][Branch1][Ring2][N][Ring1][=N][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (6r,7r)-7-[[(2r)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid\\n\",\n        \"output\": \" -0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfanyl-5-fluoro-2,4-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[2,3-dichloro-4-(thiophene-2-carbonyl)phenoxy]acetic acid\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C@@][Branch1][C][C][Branch1][C][O][C][Branch1][C][F][Branch1][C][F][F][C][Branch1][C][Cl][=C][Ring1][P]\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-chloro-7-[(3-diethylaminopropylamino)methyl]quinolin-8-ol\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring1][=C][N][C][=N][C][=C][Branch1][C][F][C][Branch1][S][N][C][C][=C][Branch1][Branch1][NH1][N][=Ring1][Branch1][C][C][C][Ring1][Ring1][=N][Ring1][S][C][=N][C][=C][Branch1][C][F][C][=N][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1-adamantylmethyl)-2-chloro-5-(piperazin-1-ylmethyl)benzamide\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(4-phenyl-1,3-thiazol-2-yl)acetamide\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(=O)Nc1ccc(cc1)S(=O)(=O)Nc2ccc(Cc3ccncc3)cc2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H12F3NO4S/c1-15(22,16(17,18)19)14(21)20-9-6-7-13-11(8-9)10-4-2-3-5-12(10)25(13,23)24/h2-8,22H,1H3,(H,20,21)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-[[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-4-yl]amino]pyrimidin-5-yl]benzamide\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring2][C][C][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][=C][Ring2][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=N][C][=Branch1][P][=C][Branch1][=Branch1][N][C][Ring1][=Branch1][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch2][Ring1][N][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][C][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" C[C@H](Nc1ncc(C)c(Nc2cc(C)[nH]n2)n1)c3ncc(F)cn3\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][Branch1][S][N][C][=N][C][=N][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1][=C][Ring1][P]\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2[nH]c(cc2c1)C(=O)N3CCN(C)CC3\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(3-methanesulfonamido-2-oxo-6-phenylpyridin-1-yl)-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H15ClN4/c1-10-12(15)14(19-8-4-5-9-19)18-13(17-10)11-6-2-3-7-16-11/h2-3,6-7H,4-5,8-9H2,1H3\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H15F2N3O3/c1-25-15-6-10-14(7-16(15)26-2)22-8-11(18(21)24)17(10)23-13-4-3-9(19)5-12(13)20/h3-8H,1-2H3,(H2,21,24)(H,22,23)\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][=N][N][Ring1][S][C][=Branch1][C][=O][C][=C][Branch1][C][F][C][=C][C][=C][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H6F3N5S/c11-10(12,13)7-4-5(6-2-1-3-19-6)15-9-16-8(14)17-18(7)9/h1-4H,(H2,14,17)\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9N3O2S2/c11-9(14)8-6(13-10(12)15)3-7(17-8)5-1-2-16-4-5/h1-4H,(H2,11,14)(H3,12,13,15)\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][F][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][=Branch1][=C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][#Branch2][=O][C][C]\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[4-chloro-2-[[(3s)-4-[2-(2-chlorophenyl)acetyl]-3-methylpiperazin-1-yl]methyl]phenoxy]acetic acid\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][C][C][O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][N][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)CCCNCc1cc(Cl)c2cccnc2c1O\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfanyl-4-methanesulfonamido-2-methylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (3s,3'r,3'as,6's,6as,6bs,7'ar,9r,11as,11br)-3',6',10,11b-tetramethylspiro[2,3,4,6,6a,6b,7,8,11,11a-decahydro-1h-benzo[i]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3h-furo[4,5-b]pyridine]-3-ol\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (6s,8s,9s,10r,11s,13s,14s,17r)-11,17-dihydroxy-17-(2-hydroxyacetyl)-6,10,13-trimethyl-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-3-one\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H14F3NO5S/c1-15(23,16(17,18)19)14(22)20-10-2-6-12(7-3-10)26(24,25)13-8-4-11(21)5-9-13/h2-9,21,23H,1H3,(H,20,22)\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1nc(cs1)c2ccccc2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C(NCc1ccccc1)c2cccnc2Oc3ccccc3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H13N3OS/c1-18-11-6-7-15-10(8-11)9-19-14-16-12-4-2-3-5-13(12)17-14/h2-8H,9H2,1H3,(H,16,17)\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C32H47N3O5S2/c1-4-35(32(36)25-26-11-13-30(14-12-26)41(3,37)38)29-17-20-33(21-18-29)22-19-31(27-9-7-6-8-10-27)28-15-23-34(24-16-28)42(39,40)5-2/h6-14,28-29,31H,4-5,15-25H2,1-3H3\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(6-aminopurin-9-yl)methyl]-5-methyl-3-(2-methylphenyl)quinazolin-4-one\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H15FN4O2S2/c1-8(6-21)17-12-11-13(20-15(22)24-11)19-14(18-12)23-7-9-4-2-3-5-10(9)16/h2-5,8,21H,6-7H2,1H3,(H2,17,18,19,20,22)/t8-/m1/s1\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCCN1c2ccccc2CCc3ccccc13\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" O=C1NN=C(Cc2ccccc2)c3ccccc13\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C7H6N2O2S2/c8-13(10,11)7-9-5-3-1-2-4-6(5)12-7/h1-4H,(H2,8,10,11)\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][O][N][C][=C][C][=C][Branch1][=N][C][=Branch1][C][=O][N][C][C][N][Branch1][C][C][C][C][Branch1][C][F][=C][Ring1][#C][=N][C][=C][Ring2][Ring1][=Branch1][F]\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][C][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H23FN4O2/c1-14-3-5-15(6-4-14)13-26-19(25)24-10-7-16(17(20)12-24)11-23-18-21-8-2-9-22-18/h2-6,8-9,16-17H,7,10-13H2,1H3,(H,21,22,23)/t16-,17-/m1/s1\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H13F3N2O4S/c1-14(22,15(16,17)18)13(21)20-10-4-6-11(7-5-10)25(23,24)12-3-2-8-19-9-12/h2-9,22H,1H3,(H,20,21)\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H9N5O/c10-8-7(9(11)15)12-13-14(8)6-4-2-1-3-5-6/h1-5H,10H2,(H2,11,15)\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc2C=CC(=O)N(CCN3CCC(CC3)NCc4cc5OCCOc5cn4)c2n1\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(CSc1ccccc1)N2CCN(CC2)c3ccccc3\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-methoxy-1h-indazole\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CNS(=O)(=O)NC1=CC=C(N(CC(=O)NC(C(C)C)C(=O)C(F)(F)F)C1=O)c2ccccc2\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][C][O][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H21NO3/c1-3-11-6-5-7-12-13-8-9-21-17(4-2,10-14(19)20)16(13)18-15(11)12/h5-7,18H,3-4,8-10H2,1-2H3,(H,19,20)\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(2,3-dihydro-[1,4]dioxino[2,3-d]pyridin-7-ylmethyl)-1-[2-(3-fluoro-6-methoxy-1,5-naphthyridin-4-yl)ethyl]piperidin-4-amine\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[(3,4-dimethoxyphenyl)amino]-8-ethylpyrido[6,5-d]pyrimidin-7-one\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[[4-[4-[(2-carboxyphenyl)amino]-3-methoxyphenyl]-2-methoxyphenyl]amino]benzoic acid\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=S(=O)(Nc1ccc(cc1)S(=O)(=O)Nc2nccs2)c3ccc4OCCOc4c3\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H13NO3/c1-16-10-6-4-9(5-7-10)12(15)13-8-2-3-11(13)14/h4-7H,2-3,8H2,1H3\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C23H32ClN3O/c24-21-2-1-16(14-27-5-3-25-4-6-27)10-20(21)22(28)26-15-23-11-17-7-18(12-23)9-19(8-17)13-23/h1-2,10,17-19,25H,3-9,11-15H2,(H,26,28)\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[2-(4-chlorophenyl)ethyl]-2-methylsulfanylpyridine-3-carboxamide\\n\",\n        \"output\": \" 3.31\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=Branch1][Ring2][=N][Ring1][=Branch1][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-[(e)-2-(3,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol\\n5-[2-(3,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H17N7O/c1-9-6-14(21-20-9)18-13-4-5-16-15(19-13)17-8-11-7-12(22-23-11)10-2-3-10/h4-7,10H,2-3,8H2,1H3,(H3,16,17,18,19,20,21)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[[4-[2-(5-ethylpyridin-2-yl)ethoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C(OCCN1CCCCC1)c2c[nH]c3ccccc23\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3,5-dinitrobenzamide\\n5-carbamoyl-n,n'-dihydroxybenzene-1,3-diamine oxide\\n3-(dihydroxyamino)-5-(dioxidoamino)benzamide\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][=C][S][C@@H1][Branch1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][C][N][C][=Branch1][C][=O][S][C][Ring2][Ring1][Ring1][=Ring1][=Branch1]\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-methylsulfinyl-2-phenyl-n-[(1s)-1-phenylpropyl]quinoline-4-carboxamide\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[(1r,2r)-2-[(5-fluoro1h-indole-2-carbonyl)amino]-2,3-dihydro-1h-inden-1-yl]acetic acid\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H11NO4/c20-14-10-15(21)23-17-12-8-4-5-9-13(12)19(18(22)16(14)17)11-6-2-1-3-7-11/h1-10,21H\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H19N3O/c1-11-3-4-13-12(9-11)10-14(16-13)15(19)18-7-5-17(2)6-8-18/h3-4,9-10,16H,5-8H2,1-2H3\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=Branch1][C][=O][N][C][C][N][Branch2][Ring1][=N][C][Branch2][Ring1][Branch1][C][C][=Branch1][C][=O][N][C][C][=C][C][=C][O][C][O][C][Ring1][Branch1][=C][Ring1][=Branch2][C][Ring2][Ring1][Ring2][C][=C][C][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][=C][N][=C][Ring1][Branch1]\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCCN(C)S(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)c2cc3cc(Cl)ccc3[nH]2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1onc(NC(=O)CSc2nc(C)cc(C)n2)c1\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cn1nc(cc1NC(=O)Nc2ccc(Cl)cc2)C(C)(C)C\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" adamantan-1-amine\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-methylaminophenyl)-1,3-benzothiazol-6-ol\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H24N2O4/c1-13(9-14-3-6-16(25-2)7-4-14)20-11-19(24)15-5-8-18(23)17(10-15)21-12-22/h3-8,10,12-13,19-20,23-24H,9,11H2,1-2H3,(H,21,22)/t13-,19+/m1/s1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H15NO2/c1-10-6-5-9-13(11(10)2)16-14-8-4-3-7-12(14)15(17)18/h3-9,16H,1-2H3,(H,17,18)\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3,5-dimethyladamantan-1-amine\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-amino-1,1-bis(4-chlorophenyl)ethanol\\n\",\n        \"output\": \" 2.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H16ClN3O4S2/c15-10-5-11-13(6-12(10)23(16,19)20)24(21,22)18-14(17-11)9-4-7-1-2-8(9)3-7/h1-2,5-9,14,17-18H,3-4H2,(H2,16,19,20)\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H9NO2/c15-12-8-11(13-6-3-7-16-13)14-10-5-2-1-4-9(10)12/h1-8H,(H,14,15)\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" O=C1C=C(N=C2N1C=Cc3ccccc23)N4CCOCC4\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-(2,4-difluorophenoxy)-8-methyl-2-(oxan-4-ylamino)pyrido[6,5-d]pyrimidin-7-one\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C@H1][C][N][Branch2][Ring1][Ring2][C][C][=C][C][Branch1][C][Cl][=C][C][=C][Ring1][#Branch1][O][C][C][=Branch1][C][=O][O][C][C][N][Ring2][Ring1][Ring1][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=Branch1][#C][=N][C][Branch1][C][N][=C][Ring1][#Branch1][C][=C][Ring1][O][O][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-[(4as,7as)-1,2,3,4,4a,5,7,7a-octahydropyrrolo[3,4-b]pyridin-6-yl]-1-cyclopropyl-6-fluoro-8-methoxy-4-oxoquinoline-3-carboxylic acid\\n\",\n        \"output\": \" -0.18\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1C=C(C(=O)O)C(=O)c2cc(F)c(N3CCNC(C)C3)c(F)c12\\n\",\n        \"output\": \" -1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][C][N][Branch2][Ring1][#Branch2][C][C][N][Branch1][=N][C][=Branch1][C][=O][C][C][C][C][C][C][Ring1][=Branch1][C][=C][C][=C][C][=N][Ring1][=Branch1][C][C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-aminophenyl)-4-[5-[(4-ethylpiperazin-1-yl)methyl]-3-methylpyridin-2-yl]benzamide\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-[[4-[2-(methyl-pyridin-2-ylamino)ethoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1[nH]c2ccccc2c1CCNCc3ccc(\\\\C=C\\\\C(=O)NO)cc3\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(cccc34)S(=O)(=O)C\\n\",\n        \"output\": \" -0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2s)-2-[[2-(benzoyl)phenyl]amino]-3-[4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]phenyl]propanoic acid\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(1,3-thiazol-2-yl)benzamide\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H12N2/c16-13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10H,(H2,16,17)\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=C][Branch2][Ring1][#Branch1][O][C][C][C][S][C][=C][C][=C][Branch1][#Branch1][C][C][=Branch1][C][=O][O][C][=C][Ring1][#Branch2][Cl][C][=C][C][C][Branch1][Ring1][C][C][=N][O][C][Ring2][Ring1][O][=Ring1][#Branch1]\\n\",\n        \"output\": \" 3.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)-n-(4-morpholin-4-ylphenyl)pyrimidin-2-amine\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-[(4-chlorophenyl)-phenylmethyl]piperazine\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" phenyl morpholine-4-carboxylate\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][#Branch1][N][C][=Branch1][C][=O][N][S][Ring1][N]\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1ccc(cc1)C2CC(=O)c3c(O)cc(O)cc3O2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(2-methoxyphenoxy)-n-methyl-3-phenylpropan-1-amine\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCC(=O)O[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H28ClN3O5S/c1-32-21-12-9-17(24)15-20(21)22(28)25-14-13-16-7-10-19(11-8-16)33(30,31)27-23(29)26-18-5-3-2-4-6-18/h7-12,15,18H,2-6,13-14H2,1H3,(H,25,28)(H2,26,27,29)\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-phenylisochromen-1-one\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H23N5OS/c27-19(26-14-7-16-5-1-2-6-18(16)15-26)17-8-12-25(13-9-17)21-23-22-20(28-21)24-10-3-4-11-24/h1-6,10-11,17H,7-9,12-15H2\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][\\\\C][=C][/C][=C][C][=C][C][=C][Ring1][=Branch1][S][C][=C][C][=C][Branch1][C][Cl][C][=C][\\\\-Ring1][#C][Ring1][#Branch1]\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H21FN6O/c1-11(2)26-12(3)23-10-17(26)16-7-8-22-19(25-16)24-13-5-6-14(15(20)9-13)18(27)21-4/h5-11H,1-4H3,(H,21,27)(H,22,24,25)\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" cellar\\n\",\n        \"output\": \" cellar is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][Branch1][S][C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch1][NH1][Ring1][=Branch2][=C][C][Branch1][Ring1][O][C][=C][Ring2][Ring1][Ring1][O][C]\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-methyl-3-oxo-2,1-benzothiazole-5-sulfonamide\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCN(CC)c1ccc2C=C(C(=O)O)C(=O)Oc2c1\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C12H14Cl2FNO4S/c1-21(19,20)8-4-2-7(3-5-8)10(17)9(6-15)16-12(18)11(13)14/h2-5,9-11,17H,6H2,1H3,(H,16,18)/t9-,10-/m1/s1\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC(c1ccccc1)c2cccnc2\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-(cyclohexylmethyl)-2-methylsulfanylpyridine-3-carboxamide\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Nc1ncnc(Nc2ccccc2)n1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCN(CCC)C(=O)c1cccc(c1)C(=O)N[C@@H](Cc2ccccc2)[C@H](O)CNCc3cccc(OC)c3\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3ccc(F)cc3)c2cc1OC\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=C][C][=Branch1][C][=O][N][Branch2][Ring1][=N][C][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][N][C][C][=C][C][O][C][C][O][C][=Ring1][=Branch1][C][=N][Ring1][#Branch2][C][Ring2][Ring1][O][=N][Ring2][Ring1][#C]\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCN[C@H]1CCc2nc(N)sc2C1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][O][C][=C][C][Branch1][N][O][C][C][C][N][C][C][C][C][Ring1][Branch1][=C][C][=N][C][=N][C][Branch2][Ring1][C][N][C][=C][Branch1][C][Cl][C][=C][C][O][C][O][C][Ring1][#Branch2][=Ring1][Branch1][=C][Ring2][Ring1][=C][Ring1][P]\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C28H27NO4S/c30-21-8-4-20(5-9-21)28-26(24-13-10-22(31)18-25(24)34-28)27(32)19-6-11-23(12-7-19)33-17-16-29-14-2-1-3-15-29/h4-13,18,30-31H,1-3,14-17H2\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[3-(4-chlorophenyl)sulfanyl-2,5-dimethylindol-1-yl]acetic acid\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H22ClNO/c19-16-4-2-1-3-15(16)17(21)20-11-18-8-12-5-13(9-18)7-14(6-12)10-18/h1-4,12-14H,5-11H2,(H,20,21)\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" snow\\n\",\n        \"output\": \" snow is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][NH1][C][=Branch1][Branch2][=C][C][Ring1][Branch1][=C][Ring1][=Branch2][C][=Branch1][C][=O][N][C][C][N][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H24N2O/c1-3-9-18(10-4-2)11-8-13-6-5-7-15-14(13)12-16(19)17-15/h5-7H,3-4,8-12H2,1-2H3,(H,17,19)\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H16O5/c1-20-12-6-4-11(5-7-12)14-10-23-16-9-13(21-2)8-15(22-3)17(16)18(14)19/h4-10H,1-3H3\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccc(CNC(=O)CSc2nc3cccnc3s2)cc1\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H27ClN2O2/c22-20-8-6-19(7-9-20)21(18-4-2-1-3-5-18)24-12-10-23(11-13-24)14-16-26-17-15-25/h1-9,21,25H,10-17H2\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][=C][N][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=Branch1][C][=O][N][C][C][C][C][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(3-methoxyphenyl)-n'-(oxolan-2-ylmethyl)quinazoline-2,4-diamine\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19ClN2O5S/c1-3-28(25,26)21-15-5-4-6-16-18(15)19(12(2)22(16)11-17(23)24)27-14-9-7-13(20)8-10-14/h4-10,21H,3,11H2,1-2H3,(H,23,24)\\n\",\n        \"output\": \" -0.29\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=C][C][C][=C][Branch1][C][C][C][=N][N][=C][Branch2][Ring1][N][S][C][C][=Branch1][C][=O][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][O][C][=C][C][=Ring1][Branch1][N][Ring2][Ring1][=Branch1][C][=Ring2][Ring1][O][C][=C][Ring2][Ring1][#C][C]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][=N][\\\\C][=C][/S][C][=Branch1][C][=S][N][C][\\\\-Ring1][=Branch1][=O][C][=C][Ring1][=C][O][C]\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H11NO2/c1-3-7(2)4-5(9)8-6(7)10/h3-4H2,1-2H3,(H,8,9,10)\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring2][O][O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][S][=Branch1][C][=O][=Branch1][C][=O][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][Ring2][Ring1][S][Cl]\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN1C(=O)N(C)c2ncn(C)c2C1=O\\n\",\n        \"output\": \" -0.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(OC)cc(c1)C2=CC=C(NC(=O)OCc3ccccc3)C(=O)N2CC(=O)NC(C(C)C)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-amino-1-phenyltriazole-4-carboxamide\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=N][C][Branch1][S][N][C][=C][C][=C][Branch1][C][F][C][Branch1][C][Cl][=C][Ring1][Branch2][=C][Ring1][#C][C][=C][Ring2][Ring1][Ring1][O][C][C][C][N][C][C][C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCCCCCN(CC)CCCC(O)c1ccc(NS(=O)(=O)C)cc1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)N(C(C)C)C(=O)C(C(CNC(=O)NCc1ccccc1F)c2ccccc2)c3cccnc3\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C@@H1][Branch1][C][C][C][=Branch1][C][=O][N][C@@H1][Branch1][=Branch2][C][C][C][C][C][C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C@H1][C][C][N][Branch1][O][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C@@H1][Ring1][P][Ring1][=C]\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" age\\n\",\n        \"output\": \" age is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOC(=O)Cc1csc(NS(=O)(=O)c2ccc(Cl)cc2)n1\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H10ClF3O3/c16-11-4-1-9(2-5-11)12-7-10(15(17,18)19)3-6-13(12)22-8-14(20)21/h1-7H,8H2,(H,20,21)\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)COc1ccc(C(=O)c2cccs2)c(Cl)c1Cl\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCCC(CC)COC(=O)CC(C(=O)OCC(CC)CCCC)S(=O)(=O)O\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1,2-bis(5-bromo-2-hydroxyphenyl)ethane-1,2-dione\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][O][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=C][N][=C][C][C][C][N][Ring1][Branch2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=Branch1][C][=N][C][=C][C][=C][Branch1][C][I][C][=C][C][=C][Ring1][#Branch1][S][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-n-(2-chloro-4-methylsulfonylphenyl)-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H21F3N4O5S/c1-11(2)16(17(28)19(20,21)22)24-15(27)10-26-14(12-6-4-3-5-7-12)9-8-13(18(26)29)25-32(23,30)31/h3-9,11,16,25H,10H2,1-2H3,(H,24,27)(H2,23,30,31)\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-[(2,5-difluorophenyl)amino]-6,7-dimethoxyquinoline-3-carboxamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3/t14-/m0/s1\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1cc(O)cc2OC=C(C(=O)c12)c3ccc(O)cc3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1ccccc1Oc2c(NS(=O)(=O)c3ccc(cc3)C(C)(C)C)nc(nc2OCCO)c4ncccn4\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" warm\\n\",\n        \"output\": \" warm is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=Branch2][Ring1][N][=N][C][=C][Branch1][N][C][=C][Branch1][C][F][C][=C][Ring1][O][Ring1][#Branch1][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)Nc1sc(cc1C(=O)N[C@H]2CCCNC2)c3ccc(F)cc3\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H13Cl2NO2S/c1-10-17(23-12-7-5-11(18)6-8-12)16-13(19)3-2-4-14(16)20(10)9-15(21)22/h2-8H,9H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)C(NC(=O)CN1C(=O)C(=CC=C1c2ccccc2)NS(=O)(=O)C(F)(F)F)C(=O)C(F)(F)F\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Oc1cc(O)c2C(=O)C=C(Oc2c1)c3ccccc3\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][O][C][C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][N][C][=Branch1][C][=O][C][=C][Branch1][C][C][NH1][C][Branch2][Ring1][Branch1][\\\\C][=C][/C][=Branch1][C][=O][N][C][=C][C][=C][Branch1][C][F][C][=C][\\\\-Ring1][O][Ring1][#Branch1][=C][Ring2][Ring1][C][C]\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)OC(=O)N1CCC(CC1)Oc2ncnc(Nc3ccc(nc3C)S(=O)(=O)C)c2C\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][P][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=Branch1][C][=O][O][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H14BrNO3S2/c1-10-4-2-3-5-11(10)16-13(17)8-9-21(18,19)14-7-6-12(15)20-14/h2-7H,8-9H2,1H3,(H,16,17)\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(carbamoylamino)-5-phenylthiophene-2-carboxamide\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" [4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl]-furan-2-ylmethanone\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" isoquinoline\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1h-indol-2-yl-(3-methylpiperazin-1-yl)methanone\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C25H25F3N4O6/c1-14(2)22(23(37)25(26,27)28)30-19(34)12-31-17(15-6-4-3-5-7-15)9-8-16(24(31)38)29-18(33)13-32-20(35)10-11-21(32)36/h3-9,14,22H,10-13H2,1-2H3,(H,29,33)(H,30,34)\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=C][C][=N][C][Branch1][#Branch2][N][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][=N]\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-(4-chlorophenyl)-3-[4-[(3r)-3-hydroxypyrrolidin-1-yl]-3-methoxyphenyl]thieno[2,3-e]triazin-4-one\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H15ClO5S/c1-2-23(20,21)13-6-3-11(4-7-13)14-9-12(17)5-8-15(14)22-10-16(18)19/h3-9H,2,10H2,1H3,(H,18,19)\\n\",\n        \"output\": \" -0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@][C][C][C@H1][C@@H1][Branch1][S][C][C][C][=C][C][Branch1][C][O][=C][C][=C][Ring1][O][Ring1][#Branch1][C@@H1][Ring1][#C][C][C][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H17Cl2N/c1-20-17-9-7-12(13-4-2-3-5-14(13)17)11-6-8-15(18)16(19)10-11/h2-6,8,10,12,17,20H,7,9H2,1H3/t12-,17-/m0/s1\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H19N3O/c1-22-18(23)13-17(21-19(22)20)11-10-14-6-5-9-16(12-14)15-7-3-2-4-8-15/h2-9,12-13H,10-11H2,1H3,(H2,20,21)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H13ClFN3/c1-11-21-9-13-10-22-18(14-4-2-3-5-16(14)20)15-8-12(19)6-7-17(15)23(11)13/h2-9H,10H2,1H3\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Br][C][=C][N][=C][Branch2][Ring1][Branch2][N][C][=C][C][=C][C][Branch1][=N][N][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Branch1][=C][Ring1][=C][N][=C][Ring2][Ring1][Branch1][N][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][S][Ring1][Branch1]\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(OCC(=O)O)c(c1)n2nc3ccccc3n2\\n\",\n        \"output\": \" -0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCCCCCN(CCc1ccc(OC(C)(C)C(=O)O)cc1)C(=O)Nc2ccc(F)cc2F\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)(C)NC(=O)C(N(Cc1occc1)C(=O)c2ccc([nH]2)c3ccccc3)c4ccncc4\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H11F4N3O4/c16-13(17)15(14(18)19)8-20(12-3-1-2-6-21(12)23)10-7-9(22(24)25)4-5-11(10)26-15/h1-7,13-14H,8H2\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCCc1c(O)c(ccc1OCc2ccc(C(=O)O)c(Br)c2)C(=O)C\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C25H28N4O4/c1-16-14-17(20-6-3-4-8-22(20)26-16)15-33-19-11-9-18(10-12-19)27-25(31)23-21(24(30)28-32)7-5-13-29(23)2/h3-4,6,8-12,14,21,23,32H,5,7,13,15H2,1-2H3,(H,27,31)(H,28,30)/t21-,23-/m0/s1\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCc1cc(OCc2ccc(cc2)c3ccccc3c4nn[nH]n4)c5CCCCc5n1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][=S][=Branch1][C][=O][Branch1][#Branch2][N][C][=C][C][=C][N][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][=C][C][=C][Branch2][Ring1][C][C][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][O][C][=C][Ring1][P]\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Ring2][C]\\n\",\n        \"output\": \" 4.21\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H23N7O2S/c1-13-5-6-15(11-19(13)31(22,29)30)24-21-23-10-9-20(25-21)27(3)16-7-8-17-14(2)28(4)26-18(17)12-16/h5-12H,1-4H3,(H2,22,29,30)(H,23,24,25)\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (2r)-3-(2-methoxyphenothiazin-10-yl)-n,n,2-trimethylpropan-1-amine\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(propan-2-ylamino)-3-(1,3-thiazol-2-yloxy)propan-2-ol\\n\",\n        \"output\": \" -0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1nc(N)c2nc(c(N)nc2n1)c3ccccc3\\n\",\n        \"output\": \" 1.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(carbamoylamino)-5-(2,3-difluorophenyl)-n-[(3s)-piperidin-3-yl]thiophene-2-carboxamide\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch2][Ring1][#C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(CN1c2ccccc2Sc3ccccc13)N(C)C\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C19H20N2O2/c1-2-3-14-17-18(22)20(15-10-6-4-7-11-15)21(19(17)23)16-12-8-5-9-13-16/h4-13,17H,2-3,14H2,1H3\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1,5-naphthyridine\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2,5-dichloro-n-(1,3-thiazol-2-yl)benzenesulfonamide\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-chloro-5-(3,5-dioxo-1,2,4-triazin-2-yl)-n-[(1-hydroxycycloheptyl)methyl]benzamide\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCCNC[C@@H](O)COc1ccccc1C(=O)CCc2ccccc2\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H26Cl2N4O/c1-22-6-2-3-14(12-22)13-23-7-9-24(10-8-23)18(25)21-15-4-5-16(19)17(20)11-15/h4-5,11,14H,2-3,6-10,12-13H2,1H3,(H,21,25)\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" pyridin-4-ylmethyl n-[2-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]-6-phenylpyridin-3-yl]carbamate\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" quinolin-2-amine\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1ccc2c(c1)c(c(C)n2CC(=O)O)c3ccnc4c(Cl)cccc34\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H21NO/c1-14-8-6-7-11-16(14)19-17(12-13-18-2)15-9-4-3-5-10-15/h3-11,17-18H,12-13H2,1-2H3/t17-/m1/s1\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 6-hydroxy-2-(4-hydroxyphenyl)chromen-4-one\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [F][C][=N][C][=C][C][=C][Ring1][=Branch1][O][C][C@@H1][C][C][N][Ring1][Ring2]\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H23F2N5O2/c1-28(2)11-16(29)12-30-17-6-4-15(5-7-17)26-20-10-21(25-13-24-20)27-19-8-3-14(22)9-18(19)23/h3-10,13,16,29H,11-12H2,1-2H3,(H2,24,25,26,27)\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch2][C][Branch1][C][Cl][=C][Ring1][#Branch1][C][=N][N][=C][C][=C][C][=C][Branch1][C][Cl][N][Ring1][#Branch2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" editor\\n\",\n        \"output\": \" editor is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-(methylcarbamoylamino)-5-phenylthiophene-2-carboxamide\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=C][O][C][=C][C][Branch1][C][O][=C][C][Branch1][C][O][=C][Ring1][Branch2][C][Ring1][N][=O]\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COC(=O)CCCCCCC(=O)Nc1ccc2C(=O)C(=O)c3ccccc3c2c1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCn1c(C)ncc1c2ccnc(Nc3ccc(cc3)S(=O)(=O)NCCOC)n2\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(N)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc3c[nH]c4ccccc34)NC=O\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H15F3O3S/c1-2-24-13-6-3-11(4-7-13)14-9-12(17(18,19)20)5-8-15(14)23-10-16(21)22/h3-9H,2,10H2,1H3,(H,21,22)\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H18F2N4O2S/c18-11-5-1-4-10(14(11)19)13-7-12(23-17(20)25)15(26-13)16(24)22-9-3-2-6-21-8-9/h1,4-5,7,9,21H,2-3,6,8H2,(H,22,24)(H3,20,23,25)/t9-/m0/s1\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H8N2O/c1-6(10)9-7-4-2-3-5-8-7/h2-5H,1H3,(H,8,9,10)\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][Branch2][Ring2][#Branch1][N][C][C][C][Branch2][Ring1][O][C][N][C][C][C][Branch1][Branch1][C][C][Ring1][=Branch1][O][C][=C][C][=C][Branch1][C][Cl][C][Branch1][C][Cl][=C][Ring1][Branch2][C][C][Ring2][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][N][C][=Branch1][C][=O][N][Branch1][C][C][C][=Branch1][C][=O][C][=C][Ring1][=Branch2][S][C][Branch2][Ring1][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F][=C][Ring1][S][C][=Branch1][C][=O][N][C][C][=C][C][Ring1][Branch1]\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-(1-cyclohexenyl)-1,5-dimethyl-1,3-diazinane-2,4,6-trione\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=Branch1][C][=O][N][C][S][C][=Branch2][Ring1][C][=C][C][=Ring1][Branch1][C][=Branch1][C][=O][N][C@H1][C][C][C][N][C][Ring1][=Branch1][C][=C][C][=C][Branch1][C][F][C][=C][Ring1][#Branch1]\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=Branch1][C][=O][C][C][C][Ring1][Ring1]\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][Branch1][C][C][C][C][Branch1][C][O][C][O][C][=C][C][=C][Branch2][Ring1][=Branch2][N][C][=C][C][Branch1][=C][N][C][=C][C][Branch1][C][C][=C][C][=C][Ring1][#Branch1][Cl][=N][C][=N][Ring1][#C][C][=C][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C19H19FN4O3/c1-12(25)22-8-15-10-24(19(26)27-15)14-4-5-18(16(20)7-14)23-9-13-3-2-6-21-17(13)11-23/h2-7,15H,8-11H2,1H3,(H,22,25)/t15-/m0/s1\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H11Cl3O2/c15-14(16,17)13(9-1-5-11(18)6-2-9)10-3-7-12(19)8-4-10/h1-8,13,18-19H\\n\",\n        \"output\": \" 3.86\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN1CCN(CCCOc2ccc(cc2)c3onc(c3)c4ccc(F)cc4)CC1\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][=C][C][=C][C][Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][Ring1][O][C][C][Branch1][Ring1][O][C][=C][Ring1][#Branch2][=N][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][C@H1][C][C@H1][Branch1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][S][C][=Branch1][#Branch1][=C][C][Ring1][N][=Ring1][Branch1][S][=Branch1][C][=O][=Branch1][C][=O][N]\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C17H26N2O4/c1-22-16-4-2-3-13(9-16)11-23-12-15(20)10-19-7-5-14(6-8-19)17(18)21/h2-4,9,14-15,20H,5-8,10-12H2,1H3,(H2,18,21)\\n\",\n        \"output\": \" -0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C13H19NO4S/c1-3-9-14(10-4-2)19(17,18)12-7-5-11(6-8-12)13(15)16/h5-8H,3-4,9-10H2,1-2H3,(H,15,16)\\n\",\n        \"output\": \" 0.03\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H29N5O6S/c1-13(2)31-21(27)26-10-8-15(9-11-26)32-20-18(30-4)19(22-12-23-20)25-16-6-7-17(24-14(16)3)33(5,28)29/h6-7,12-13,15H,8-11H2,1-5H3,(H,22,23,25)\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-cyclopropyl-3-phenyl-[1,2,4]triazolo[3,4-f]pyridazin-6-amine\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(5-amino-1-phenyl-1,2,4-triazol-3-yl)acetamide\\n\",\n        \"output\": \" -0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C10H17N/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2\\n\",\n        \"output\": \" -0.98\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-n-[2-chloro-4-(3-hydroxypropylsulfamoyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][Branch2][Ring1][P][N][N][C][=Branch1][C][=O][C][=C][Branch1][Branch1][C][Ring1][#Branch1][=O][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][Cl][C][=C][Ring1][#Branch1][N][Ring1][=C][C][=C][C][=N][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (1s)-1-[5-[(4-fluorophenyl)methylsulfonyl]-1,3,4-oxadiazol-2-yl]-3-methylbutan-1-amine\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][N][C][Branch1][C][C][=N][C][=C][Ring1][=Branch1][C][=N][C][Branch2][Ring1][N][N][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=N][C][=C][Ring2][Ring1][#Branch1][F]\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][N][C][C][N][Branch1][Branch1][C][C][Ring1][=Branch1][C][=C][C][=C][N][=C][N][Branch1][O][C][=Branch1][C][=O][C][Ring1][#Branch1][=C][Ring1][O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][C][C][=Branch1][C][=O][N][C][C][C][C][Ring1][Ring2]\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C15H13NO3/c17-14(10-4-2-1-3-5-10)13-7-6-12-11(15(18)19)8-9-16(12)13/h1-7,11H,8-9H2,(H,18,19)\\n\",\n        \"output\": \" -0.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Cl][C][=C][C][=C][C][=C][Ring1][=Branch1][C][C][N][C][=Branch1][C][=O][C][=C][C][=Branch1][#Branch1][=C][C][=C][Ring1][=Branch1][Cl][N][N][=C][C][=Branch1][C][=O][N][C][Ring1][#Branch1][=O]\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O][C][=C][C][=Branch1][C][=O][C][=C][Branch1][Ring2][O][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring2][Ring1][C][=O]\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H12Cl2N2O3/c19-10-8-13(20)16-12(17(18(24)25)22-14(16)9-10)6-7-15(23)21-11-4-2-1-3-5-11/h1-9,22H,(H,21,23)(H,24,25)/b7-6+\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H13NO2/c18-16(19)14-11-17(10-12-6-2-1-3-7-12)15-9-5-4-8-13(14)15/h1-9,11H,10H2,(H,18,19)\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(3-ethyl-5-phenylimidazol-4-yl)-[1,3]thiazolo[4,5-e]pyrimidin-7-amine\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-chloro-3-[1-[3-(2-oxo-3h-benzimidazol-1-yl)propyl]piperidin-4-yl]-1h-benzimidazol-2-one\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-methyl-4-phenyl-3,4-dihydro-1h-isoquinolin-8-amine\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-methyl-2-[[3-[(e)-2-pyridin-2-ylethenyl]-1h-indazol-6-yl]sulfanyl]benzamide\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" trout\\n\",\n        \"output\": \" trout is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" toothpaste\\n\",\n        \"output\": \" toothpaste is not a SMILES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[5-(4-fluorophenyl)-2-(4-methylsulfanylphenyl)-3h-imidazol-4-yl]pyridine\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=C][C][=Branch2][Ring2][Ring2][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][C][=C][C][=Branch1][S][=N][C][=Branch1][Ring2][=N][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][N][C][C][O][C][C][Ring1][=Branch1][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=N][C][=C][Branch1][=Branch1][C][=Branch1][C][=O][N][C][Branch1][=C][N][C][=C][C][=C][C][Branch1][C][Cl][=C][Ring1][#Branch1][Cl][=C][Ring2][Ring1][C][C][=C][Ring2][Ring1][=Branch1][O][C]\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C12H6Cl3N3/c13-7-3-1-4-8(14)11(7)12-17-16-10-6-2-5-9(15)18(10)12/h1-6H\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C16H17F2N5O2S2/c1-16(6-24,7-25)23-13-11-12(20-14(19)27-11)21-15(22-13)26-5-8-3-2-4-9(17)10(8)18/h2-4,24-25H,5-7H2,1H3,(H3,19,20,21,22,23)\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNC1=Nc2ncccc2C(=NC1c3cccs3)c4occc4\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" pyridine-4-carbohydrazide\\n\",\n        \"output\": \" -0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" C[C@@H]1CN(Cc2cc(Cl)ccc2OCC(=O)O)C[C@H](C)N1C(=O)Cc3ccccc3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch1][C][C][C][Branch2][Ring1][O][N][C][=Branch1][C][=O][C][C][C][C][C][C][Branch1][O][C][C][Branch1][Ring2][C][Ring1][=Branch1][C][Ring1][=Branch2][C][Ring1][#Branch2][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 3.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-(dibutylamino)propyl 4-aminobenzoate\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C32H41N5O4/c1-4-8-29(38)32(24-9-6-5-7-10-24)15-17-37(18-16-32)31(40)28(19-23-11-13-26(41-3)14-12-23)35-30(39)27(33)20-25-21-34-22-36(25)2/h5-7,9-14,21-22,27-28H,4,8,15-20,33H2,1-3H3,(H,35,39)/t27-,28+/m0/s1\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C18H13ClF3NO3/c1-10-17(26-13-5-3-12(19)4-6-13)14-8-11(18(20,21)22)2-7-15(14)23(10)9-16(24)25/h2-8H,9H2,1H3,(H,24,25)\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(C)COc1cc(OC(C)C)cc(c1)C(=O)Nc2ccc(cn2)C(=O)O\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C][C][=C][C][=C][Branch2][Ring1][=Branch1][O][C][C][=C][C][=C][C][Branch1][#Branch2][O][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Ring1][=N][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=Branch2][Ring1][Branch2][=C][C][Branch1][Branch2][N][C][C][C][C][Ring1][Branch1][=C][Ring1][O][O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" -0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n'-(1h-indazol-4-yl)-n'-methyl-n-(3-methylsulfonylphenyl)pyrimidine-2,4-diamine\\n\",\n        \"output\": \" 3.21\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCCCNCCCOc1ccc(Cl)c(c1)C(=O)NCC23CC4CC(CC(C4)C2)C3\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CCOC(=O)C1(CCN(C)CC1)c2ccccc2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" OC1(CNCCc2ccccc12)c3ccccc3\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][S][=Branch1][C][=O][=Branch1][C][=O][N][C][=C][C][=C][Branch2][Ring2][Ring2][N][Branch2][Ring1][O][C][C][=Branch1][C][=O][N][C][Branch1][=Branch1][C][Branch1][C][C][C][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F][C][Ring2][Ring1][Ring2][=O][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H8O2/c15-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(13)16/h1-8H\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][=Branch1][C][N][C][=Branch1][C][=O][C][S][C][=N][C][=C][C][=C][N][=C][Ring1][=Branch1][S][Ring1][=Branch2][C][=C][Ring2][Ring1][Branch1]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C@H1][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][=N][C][Branch2][Ring1][=C][N][C][=C][C][=C][Branch1][#Branch1][C][=C][Ring1][=Branch1][O][C][C][=Branch1][C][=O][N][C][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][=N][C][=C][Ring2][Ring1][=Branch2][N][Branch1][C][C][C][Ring2][Ring2][Ring1][=O]\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CN4CCC[C@H]4C(=O)N\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 5-ethyl-3-methyl-5-phenylimidazolidine-2,4-dione\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 1-(4-methylphenyl)-2h-pyrazolo[5,4-b]pyridin-3-one\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4,5-dichloro-2-(4,6-dimethoxypyrimidin-2-yl)pyridazin-3-one\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 8-[4-(4-hydroxyphenyl)phenyl]-1-azabicyclo[2.2.2]octan-8-ol\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [O][C][C][=Branch1][C][=O][N][C][C][C][C@@H1][Ring1][Branch1][C][O][C][=C][C][=C][C][=N][C][=N][C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][Branch1][O][O][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][Branch1][C][Cl][=C][Ring1][#C][=C][Ring2][Ring1][#Branch2][Ring2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C@@H1][Branch1][C][C][N][C][C][C][C][=C][C][=C][C][=C][Ring1][=Branch1][Cl]\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H27N5O9S2/c1-9(2)33-21(30)35-10(3)34-19(29)15-11(6-31-4)7-36-18-14(17(28)26(15)18)24-16(27)13(25-32-5)12-8-37-20(22)23-12/h8-10,14,18H,6-7H2,1-5H3,(H2,22,23)(H,24,27)/b25-13-/t10?,14-,18-/m1/s1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNc1cc(nc2c(cc(OC)cc12)N3CCN(C)CC3)C(=O)Nc4ccc(cc4)N5CCOCC5\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Clc1ccc(N2CCN(CC2)C(=O)COCc3ccncc3)c(Cl)c1\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" phenylmethyl n-[2-cyclohexyl-6-oxo-1-[2-oxo-2-[(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)amino]ethyl]pyrimidin-5-yl]carbamate\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" skin\\n\",\n        \"output\": \" skin is not a SELFIES and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C13H10ClNO/c14-11-6-4-10(5-7-11)13(16)9-12-3-1-2-8-15-12/h1-8H,9H2\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C18H19FN4O4S/c1-12-9-22(21-20-12)10-15-11-23(18(24)27-15)14-2-3-16(17(19)8-14)13-4-6-28(25,26)7-5-13/h2-4,8-9,15H,5-7,10-11H2,1H3/t15-/m0/s1\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-[5-(1-adamantylmethylcarbamoyl)-6-chloroquinolin-2-yl]benzoic acid\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[1-[3-(4-acetylpiperidin-1-yl)-3-phenylpropyl]piperidin-4-yl]-n-ethyl-2-(4-methylsulfonylphenyl)acetamide\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" (3s,4r)-3-ethyl-4-[(3-methylimidazol-4-yl)methyl]oxolan-2-one\\n\",\n        \"output\": \" -0.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H17NO4/c1-3-21-17(20)16-11(2)18(10-13-5-4-8-22-13)15-7-6-12(19)9-14(15)16/h4-9,19H,3,10H2,1-2H3\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 4-hydroxy-n-(4-hydroxyphenyl)benzamide\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][=C][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=C][N+1][Branch1][C][O-1][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-(4-bromophenyl)-2,3-dihydro-1h-quinazolin-4-one\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C20H24N2O3S/c1-16(21)20(23)22-18(13-12-17-8-4-2-5-9-17)14-15-26(24,25)19-10-6-3-7-11-19/h2-11,14-16,18H,12-13,21H2,1H3,(H,22,23)/b15-14+/t16-,18-/m0/s1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][=N][C][C][=C][C][=C][Branch1][C][O][C][=C][Ring1][#Branch1][N][C][C][Branch1][C][O][C][=C][C][Branch1][C][O][=C][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" -0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [N][C][=N][C][=C][C][=C][C][=C][C][=C][Ring1][#Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1c(Sc2ccc(Cl)cc2)c3cc(ccc3n1CC(=O)O)S(=O)(=O)C\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1c(CC(=O)O)c2cc(F)ccc2n1S(=O)(=O)c3ccc(cc3)S(=O)(=O)C\\n\",\n        \"output\": \" -0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C20H14ClN3O5/c1-29-20(28)11-4-2-10(3-5-11)9-24-19(27)15-16(18(26)23-24)22-14-8-12(21)6-7-13(14)17(15)25/h2-8H,9H2,1H3,(H,22,25)(H,23,26)\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C27H34N6O3/c1-28-23-18-24(27(34)29-19-4-6-20(7-5-19)32-12-14-36-15-13-32)30-26-22(23)16-21(35-3)17-25(26)33-10-8-31(2)9-11-33/h4-7,16-18H,8-15H2,1-3H3,(H,28,30)(H,29,34)\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C1Cc2ccccc2CN1c3ccncc3\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H29Cl2N3O3/c1-23(2,3)21(30)27-14-16-5-8-18(9-6-16)28-22(31)29-12-4-11-24(32,15-29)17-7-10-19(25)20(26)13-17/h5-10,13,32H,4,11-12,14-15H2,1-3H3,(H,27,30)(H,28,31)\\n\",\n        \"output\": \" 3.93\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)COc1ccc(OCCNCC(O)COc2ccccc2)cc1\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][Branch1][Ring1][C][O][N][C][=N][C][Branch1][#C][S][C][C][=C][C][=C][C][Branch1][C][F][=C][Ring1][#Branch1][F][=N][C][=N][C][Branch1][C][N][=C][N][=C][Ring2][Ring1][Branch1][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC(=O)c1cc2cc(ccc2n1Cc3ccc(Cl)c(Cl)c3)C(F)(F)F\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C@H1][C][C@H1][C@@H1][C][C][C@][Branch1][C][O][Branch1][=Branch1][C][=Branch1][C][=O][C][C@@][Ring1][=Branch2][Branch1][C][C][C][C@H1][Branch1][C][O][C@][Ring1][#C][Branch1][C][F][C@@][Branch1][C][C][C][=C][C][=Branch1][C][=O][C][=C][Ring2][Ring1][#Branch2][Ring1][Branch2]\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-(phenylcarbamoylamino)benzoic acid\\n\",\n        \"output\": \" -0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" C(CNCc1ccccc1)NCc2ccccc2\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][S][C][=N][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][C][N][S][Ring1][=Branch2]\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-5-methylpyrazine-2-carboxamide\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][=Branch2][N][C][=C][C][=C][C][Branch1][=C][N][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][=N][Ring1][#C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 4.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r,3r,4s,5r)-2-(6-amino-2-butylsulfanylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCOc1ccc2nc(N)sc2c1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1ccc(Nc2c(F)cccc2Cl)c(CC(=O)O)c1\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H29ClN4O5/c27-19-3-4-21-25(35-16-34-21)24(19)30-26-23-20(28-15-29-26)13-18(33-12-9-31-7-1-2-8-31)14-22(23)36-17-5-10-32-11-6-17/h3-4,13-15,17H,1-2,5-12,16H2,(H,28,29,30)\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=C][C][Branch1][C][O][=C][C][=Branch1][C][=O][C][=Branch1][=Branch2][=C][O][C][Ring1][#Branch1][=C][Ring1][N][C][=C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Ring1][Branch2]\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C26H32N8O3S/c1-32-12-14-34(15-13-32)38(36,37)21-6-4-19(5-7-21)23-17-29-25(27)24(30-23)26(35)31-22-16-28-9-8-20(22)18-33-10-2-3-11-33/h4-9,16-17H,2-3,10-15,18H2,1H3,(H2,27,29)(H,31,35)\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3-phenyl-7-propan-2-yloxychromen-4-one\\n\",\n        \"output\": \" 4.07\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-ethyl-3-methylpyrrolidine-2,5-dione\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C19H18ClN3O3S2/c1-28(26)7-6-23-15-5-3-2-4-11(15)8-14(19(23)25)21-17(24)13-9-12-10-16(20)27-18(12)22-13/h2-5,9-10,14,22H,6-8H2,1H3,(H,21,24)\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-[1-(1h-benzimidazol-2-yl)-3-phenylbutan-2-yl]-1h-benzimidazole\\n\",\n        \"output\": \" 4.48\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccccc1c2ccc3c(c2)C(=O)C(=O)c4ccccc34\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][C][=C][Branch1][C][C][N][=C][S][C][Branch1][=Branch1][C][=Branch1][C][=O][N][=C][Branch1][C][N][C][Ring1][=Branch2][=C][Ring1][=C][C]\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [2-hydroxy-3-(2-methoxyphenoxy)propyl] carbamate\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C15H17FN4O3/c1-2-19-8-10(15(22)23)12(21)9-7-11(16)14(18-13(9)19)20-5-3-17-4-6-20/h7-8,17H,2-6H2,1H3,(H,22,23)\\n\",\n        \"output\": \" -0.83\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][Branch2][Ring1][S][C][=Branch1][C][=O][N][C][C][=C][C][=C][Branch1][=N][C][N][C][C][N][Branch1][C][C][C][C][Ring1][#Branch1][C][=C][Ring1][=C][C][Ring1][P][=C][Branch1][C][O][C][=C][Ring2][Ring1][#Branch2][O]\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C32H41NO2/c1-31(2,3)26-18-16-25(17-19-26)30(34)15-10-22-33-23-20-29(21-24-33)32(35,27-11-6-4-7-12-27)28-13-8-5-9-14-28/h4-9,11-14,16-19,29-30,34-35H,10,15,20-24H2,1-3H3\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring1][N][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=N][=C][N][=C][Ring1][#Branch1][C][=C][C][=C][S][Ring1][Branch1][N][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [N][C][=N][C][=N][C][NH1][C][=C][C][Ring1][=Branch2][=Ring1][Branch1]\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][Branch2][Ring1][#Branch1][N][Branch1][Branch1][C][C][C][N][C][=Branch1][C][=O][C][=C][C][=C][Branch1][C][C][C][=C][Ring1][#Branch1][C][=N][C][S][N][=C][Branch1][C][C][C][=Ring1][=Branch1][C][=Branch1][C][=O][N][Ring1][O][C][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" COc1ccc(OC(F)(F)F)cc1CN[C@H]2CCCN[C@H]2c3ccccc3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" COc1ccc(cc1)c2nc3CCCn3c2Br\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CN(C(=O)C)c1ccccc1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H24N4O2/c1-15-12-18(16(2)22-17-6-4-3-5-7-17)21-23-19(13-20(26)25(21)14-15)24-8-10-27-11-9-24/h3-7,12-14,16,22H,8-11H2,1-2H3\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][N][C][=Branch1][C][=O][C][=C][Branch2][Ring1][Branch1][C][C][C][=C][C][=C][C][=Branch1][Ring2][=C][Ring1][=Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][=C][Ring2][Ring1][Branch1][N]\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" CC(C)Oc1cc(OCCN2CCOCC2)cc3ncnc(Nc4c(Cl)ccc5OCOc45)c13\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)n1c(C)ncc1c2ccnc(Nc3ccc(C(=O)NCCN(C)C)c(F)c3)n2\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(4-chloro-2-fluorophenyl)-6-methoxy-7-(piperidin-4-ylmethoxy)quinazolin-4-amine\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)c1ccc(cc1)S(=O)(=O)NC(=O)NC2CCCCC2\\n\",\n        \"output\": \" -0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" n-(2-aminophenyl)pyridine-2-carboxamide\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][C][=Branch1][C][=O][C][C@H1][C@@H1][Branch1][N][C][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1][N][C][=Branch1][C][=O][C][=C][C][S][C][Branch1][C][Cl][=C][Branch1][C][Cl][C][=Ring1][#Branch1][NH1][Ring1][#Branch2]\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C15H11NO2/c17-15(16-12-7-2-1-3-8-12)14-10-11-6-4-5-9-13(11)18-14/h1-10H,(H,16,17)\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C9H11FN2O/c10-9-8(2-1-4-12-9)13-6-7-3-5-11-7/h1-2,4,7,11H,3,5-6H2/t7-/m0/s1\\n\",\n        \"output\": \" -1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 4-oxo-4-[(2-propylsulfanyl-1,3-benzothiazol-6-yl)amino]butanoic acid\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCCC(=O)Nc1ccc(OCC(O)CNC(C)C)c(c1)C(=O)C\\n\",\n        \"output\": \" -0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 3-amino-6-[2-methyl-4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-pyridin-3-ylpyrazine-2-carboxamide\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" N(c1ccccc1)c2ncnc3ccccc23\\n\",\n        \"output\": \" 2.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCCN(CCO)c1nc(N2CCCCC2)c3nc(nc(N4CCCCC4)c3n1)N(CCO)CCO\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" n-[(4-methoxyphenyl)methyl]-n',n'-dimethyl-n-pyridin-2-ylethane-1,2-diamine\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][=Branch1][C][=O][C][=C][Branch1][C][C][C][=C][N][=C][Branch2][Ring1][Ring2][N][C][=C][C][=C][Branch1][Branch1][C][=N][Ring1][=Branch1][N][C][C][N][C][C][Ring1][=Branch1][N][=C][Ring2][Ring1][Ring1][N][Branch1][Branch2][C][C][C][C][C][Ring1][Branch1][C][Ring2][Ring1][=N][=O]\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [O-1][N+1][=Branch1][C][=O][C][=C][C][=C][C][=Branch1][C][=O][C][=Branch1][C][=O][C][=C][C][=C][C][=C][Ring1][=Branch1][C][Ring1][N][=C][Ring1][S]\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Cc1cc(C)nc(N)c1\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 7-chloro-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-1,4-benzodiazepin-2-one\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 1,2-di(phenyl)-4-(2-phenylsulfinylethyl)pyrazolidine-3,5-dione\\n\",\n        \"output\": \" -0.51\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-[4-chloro-3-([1,3]oxazolo[4,5-b]pyridin-2-yl)phenyl]butanamide\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C26H25N5O2/c1-17(2)15-30-24-22(25(32)29(3)26(30)33)23(19-11-13-27-14-12-19)31(28-24)16-20-9-6-8-18-7-4-5-10-21(18)20/h4-14,17H,15-16H2,1-3H3\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" [(3s,5s,8r,9s,10s,13r,14s,17r)-10-formyl-5,14-dihydroxy-13-methyl-17-(5-oxo-2h-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] acetate\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 3,3,3-trifluoro-2-hydroxy-2-methyl-n-[4-(phenylsulfamoyl)phenyl]propanamide\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C16H14N6S/c1-2-22-9-20-11(10-6-4-3-5-7-10)13(22)16-21-12-14(17)18-8-19-15(12)23-16/h3-9H,2H2,1H3,(H2,17,18,19)\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C10H9N3O2S/c1-13-10(15)12-9(16-13)11-8(14)7-5-3-2-4-6-7/h2-6H,1H3,(H,11,12,14,15)\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][C][Branch2][Ring1][#Branch2][N][C][=N][C][=C][C][Branch1][#C][N][C][=C][C][=C][C][NH1][N][=C][C][Ring1][=Branch2][=Ring1][Branch1][=N][Ring1][S][=C][Ring2][Ring1][#Branch1]\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C18H19Cl2N3O2/c19-14-4-5-17(16(20)11-14)22-7-9-23(10-8-22)18(24)13-25-12-15-3-1-2-6-21-15/h1-6,11H,7-10,12-13H2\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch1][Ring1][C][C][S][=Branch1][C][=O][=Branch1][C][=O][C][=C][C][=C][Branch2][Ring1][Branch1][N][C][=Branch1][C][=O][C][Branch1][C][C][Branch1][C][O][C][Branch1][C][F][Branch1][C][F][F][C][=C][Ring1][S]\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][N][=C][Branch1][Ring2][N][Ring1][Branch1][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2]\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 2-[5-amino-2-(3,5-difluorophenyl)-6-oxopyrimidin-1-yl]-n-(1,1,1-trifluoro-4-methyl-2-oxopentan-3-yl)acetamide\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCOC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)c2cccc3ccccc23\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C@H1][Branch2][Ring2][Branch2][C][O][C][=C][N][N][=C][N][=C][Branch2][Ring1][Ring1][O][C][=C][C][=C][NH1][C][Branch1][C][C][=C][C][Ring1][=Branch1][=C][Ring1][#Branch2][F][C][Ring2][Ring1][C][=C][Ring2][Ring1][Branch1][C][O][C][=Branch1][C][=O][C@H1][Branch1][C][C][N]\\n\",\n        \"output\": \" 3.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(OC)n1\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CCc1cccc2c3CCOC(CC)(CC(=O)O)c3[nH]c12\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C21H27N5/c22-12-3-4-14-26(15-20-24-17-9-1-2-10-18(17)25-20)19-11-5-7-16-8-6-13-23-21(16)19/h1-2,6,8-10,13,19H,3-5,7,11-12,14-15,22H2,(H,24,25)\\n\",\n        \"output\": \" 0.83\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 5-butyl-5-ethyl-1,3-diazinane-2,4,6-trione\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-pyridin-3-yl-2,3-dihydro-1,4-benzodioxine-7-sulfonamide\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OC[C@H]1C[C@H]([C@H](O)[C@@H]1O)n2nnc3c(N[C@@H]4C[C@H]4c5ccc(F)c(F)c5)nc(SCCC(F)(F)F)nc23\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN(C)CCNS(=O)(=O)c1ccc(Nc2nccc(n2)c3cnc4ccccn34)cc1\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" COc1cccc2[nH]ncc12\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H25ClN2O5S/c22-19-7-8-20(29-15-21(25)26)18(13-19)14-23-9-4-10-24(12-11-23)30(27,28)16-17-5-2-1-3-6-17/h1-3,5-8,13H,4,9-12,14-16H2,(H,25,26)\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C13H10N4/c1-2-6-12-11(5-1)13(16-9-15-12)17-10-4-3-7-14-8-10/h1-9H,(H,15,16,17)\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[5-fluoro-4-(2-methyl-3-propan-2-ylimidazol-4-yl)pyrimidin-2-yl]amino]-n-(1-methylpiperidin-4-yl)benzamide\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C14H12O4/c15-11-5-10(6-12(16)8-11)2-1-9-3-4-13(17)14(18)7-9/h1-8,15-18H/b2-1+\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C14H17N3OS2/c1-9-10(2)20-14-12(9)13(15-8-16-14)19-7-11(18)17-5-3-4-6-17/h8H,3-7H2,1-2H3\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2-(4-chlorophenyl)-4-(trifluoromethyl)phenoxy]acetic acid\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Clc1ccc(CN2C[C@@H]3C[C@H]2CN3)cc1C(=O)NCC45CC6CC(CC(C6)C4)C5\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Cc1cc(C)cc(c1)c2[nH]c3ccccc3c2CCNCCCCc4ccncc4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" Cc1cnc(NC(=O)Cc2ccccc2)s1\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" NC(=O)C1=CN(Cc2ccc(Cl)cc2Cl)C(=O)C=C1\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C21H21FN4O2/c22-18-7-6-14(12-17(18)21(28)26-10-3-8-23-9-11-26)13-19-15-4-1-2-5-16(15)20(27)25-24-19/h1-2,4-7,12,23H,3,8-11,13H2,(H,25,27)\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [Br][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][N][C][=N][C][=C][C][=C][C][=C][Ring1][=Branch2][Ring1][=Branch1]\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CCN1CCC[C@H]1CNC(=O)c2cc(Br)cc(OC)c2OC\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-amino-n-[(2r)-1-[(3r)-3-(dimethylamino-methylcarbamoyl)-3-(phenylmethyl)piperidin-1-yl]-3-(1h-indol-3-yl)-1-oxopropan-2-yl]-2-methylpropanamide\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CC(=O)NC[C@H]1CN(C(=O)O1)c2ccc(N3Cc4cccnc4C3)c(F)c2\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 7-(phenylmethoxy)chromen-4-one\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C11H17NO/c1-8-5-4-6-9(2)11(8)13-7-10(3)12/h4-6,10H,7,12H2,1-3H3\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 3-phenyldiazenylpyridine-2,6-diamine\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CNc1cccc(CCCc2ccc(C[C@H](NC(=O)c3c(Cl)cccc3Cl)C(=O)O)s2)n1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" (2s)-n-tert-butyl-1-[(2s,4r)-2-hydroxy-5-[[(1s,2r)-2-hydroxy-2,3-dihydro-1h-inden-1-yl]amino]-5-oxo-4-(phenylmethyl)pentyl]-4-(pyridin-3-ylmethyl)piperazine-2-carboxamide\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H25NO3/c1-26-22-9-6-17(15-20(22)16-24-10-12-27-13-11-24)14-19-8-7-18-4-2-3-5-21(18)23(19)25/h2-6,9,14-15H,7-8,10-13,16H2,1H3/b19-14-\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][N][Branch2][Ring2][N][C][C][C][N][Branch2][Ring1][S][C][C][C][Branch1][=Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C][C][C][Ring2][Ring1][=Branch2][C][=Branch1][C][=O][C][C][=C][C][=C][Branch1][Branch1][C][=C][Ring1][=Branch1][S][=Branch1][C][=O][=Branch1][C][=O][C]\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C24H27FN6O3/c1-33-22-5-3-19-23(30-22)17(18(25)13-27-19)8-11-31-9-6-15(7-10-31)26-12-16-2-4-20-24(28-16)29-21(32)14-34-20/h2-5,13,15,26H,6-12,14H2,1H3,(H,28,29,32)\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][Branch2][Ring2][O][N][C][=Branch1][C][=O][C][N][C][=Branch1][C][=O][C][=Branch1][=C][=C][C][=C][Ring1][#Branch1][C][=C][C][=C][C][=C][Ring1][=Branch1][N][C][=Branch1][C][=O][N][C][C][=C][C][=N][C][=C][Ring1][=Branch1][C][=Branch1][C][=O][C][Branch1][C][F][Branch1][C][F][F]\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2r)-2-[[2-amino-5-(phenylmethylsulfanyl)-[1,3]thiazolo[5,4-e]pyrimidin-7-yl]amino]butan-1-ol\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" Fc1ccc(cc1)C(=O)C2CCN(CC2)C(=O)N3CCOCC3\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" (2s,3as,6as)-1-[(2s)-2-[[(2s)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]propanoyl]-3,3a,4,5,6,6a-hexahydro-2h-cyclopenta[d]pyrrole-2-carboxylic acid\\n\",\n        \"output\": \" -0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" methyl 2-(4-hydroxyphenoxy)acetate\\n\",\n        \"output\": \" 0.92\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CC(C)(C(=O)N)C(=O)NCCCNc1nc(Nc2cccc(NC(=O)N3CCCC3)c2)ncc1Br\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34)\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C28H27N7O3/c1-19(28(36)34-11-13-37-14-12-34)38-25-7-4-6-23-26(25)27(31-18-30-23)33-21-8-9-24-20(15-21)16-32-35(24)17-22-5-2-3-10-29-22/h2-10,15-16,18-19H,11-14,17H2,1H3,(H,30,31,33)/t19-/m1/s1\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" n-(3-chlorophenyl)sulfonyl-4-[4-(3,4-dichlorophenoxy)piperidin-1-yl]piperidine-1-carboxamide\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C22H22F3N3O5S2/c1-12(2)28-20-17(18(29)26(3)21(28)31)16(19(30)27-8-9-35(32,33)11-27)15(34-20)10-13-6-4-5-7-14(13)22(23,24)25/h4-7,12H,8-11H2,1-3H3\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C21H31N5O2/c27-18-16-21(6-1-2-7-21)17-19(28)26(18)11-4-3-10-24-12-14-25(15-13-24)20-22-8-5-9-23-20/h5,8-9H,1-4,6-7,10-17H2\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 2-hydroxy-1,2-di(phenyl)-3-piperidin-1-ylpropan-1-one\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C17H16N4/c18-17-16(7-3-9-20-17)21-11-13-4-1-5-14(10-13)15-6-2-8-19-12-15/h1-10,12,21H,11H2,(H2,18,20)\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" OCCNC(=O)CN1C(=O)C(Cc2ccccc12)NC(=O)c3cc4cc(Cl)sc4[nH]3\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 5-ethyl-5-phenyl-1,3-diazinane-2,4,6-trione\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=S(=O)(Nc1cccc2[nH]ncc12)c3cccs3\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C24H21N3O4/c1-30-16-12-13-19-18(14-16)21(15-8-4-3-5-9-15)26-22(24(29)25-19)27-23(28)17-10-6-7-11-20(17)31-2/h3-14,22H,1-2H3,(H,25,29)(H,27,28)\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [C][C][C][C][=C][Branch1][C][O][C][Branch1][C][O][=C][Branch1][=Branch1][C][=Branch1][C][=O][O][C][=C][C][Branch1][#Branch2][C][C][=C][C][=C][C][=C][Ring1][=Branch1][=C][Branch1][C][C][C][=C][Ring2][Ring1][#Branch1][Ring1][=C]\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SELFIES? ->\",\n        \"input\": \" [F][C][=C][C][=C][Branch2][Ring1][P][S][C][=N][N][C][=N][C][=Branch1][C][=O][C][=Branch1][Branch2][=C][Ring1][#Branch1][C][=C][Ring1][O][C][=C][Branch1][C][Cl][C][=C][C][=C][Ring1][#Branch1][Cl][C][Branch1][C][F][=C][Ring2][Ring1][O]\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" CN1CCN(CC1)C(=O)Cc2csc(NS(=O)(=O)c3cccc(Cl)c3C)n2\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1,3-benzothiazole-2-sulfonamide\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C17H24N2O2S/c1-17(16(21)18-13-6-3-2-4-7-13)10-9-15(20)19(17)12-14-8-5-11-22-14/h5,8,11,13H,2-4,6-7,9-10,12H2,1H3,(H,18,21)\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C23H29N3O2S2/c1-24(2)30(27,28)18-10-11-23-21(17-18)19(20-7-4-5-9-22(20)29-23)8-6-12-26-15-13-25(3)14-16-26/h4-5,7-11,17H,6,12-16H2,1-3H3/b19-8-\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 2-[2,5-dimethyl-3-(8-methylquinolin-4-yl)indol-1-yl]acetic acid\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C8H6ClN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given SMILES, write its lipophilicity. ->\",\n        \"input\": \" CN[C@@H](C)[C@H](O)c1ccccc1\\n\",\n        \"output\": \" -1.15\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given InChI. ->\",\n        \"input\": \" InChI=1S/C7H13NO/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2,(H2,8,9)\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given IUPAC? ->\",\n        \"input\": \" 4-[[4-(2,3-dimethylimidazol-4-yl)pyrimidin-2-yl]amino]benzenesulfonamide\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" 1-pyridin-4-ylbenzotriazole\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" step\\n\",\n        \"output\": \" step is not a InChI and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][C][Branch1][C][C][C][=C][C][=C][O][C][=N][C][Branch1][C][N][=C][Branch1][#C][C][=C][Ring1][#Branch1][C][=Branch1][C][=O][C][Ring1][N][=C][Ring1][S][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given SELFIES, write its lipophilicity. ->\",\n        \"input\": \" [C][O][C][=C][C][=C][Branch2][Ring1][Ring2][C][N][Branch1][Branch2][C][C][N][Branch1][C][C][C][C][=C][C][=C][C][=N][Ring1][=Branch1][C][=C][Ring2][Ring1][Ring1]\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given InChI, write its lipophilicity. ->\",\n        \"input\": \" InChI=1S/C23H29N7O2/c1-16(2)30-17(3)25-14-21(30)20-8-9-24-23(27-20)26-18-4-6-19(7-5-18)28-10-12-29(13-11-28)22(32)15-31/h4-9,14,16,31H,10-13,15H2,1-3H3,(H,24,26,27)\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C31H30N4O4/c1-22-8-11-25(33-31(37)24-5-4-7-27(19-24)35-15-17-38-18-16-35)20-29(22)34-30(36)23-9-12-28(13-10-23)39-21-26-6-2-3-14-32-26/h2-14,19-20H,15-18,21H2,1H3,(H,33,37)(H,34,36)\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [C][C][Branch2][Ring1][=C][C][C][C][=C][C][=C][C][Branch1][P][O][C][C][=C][C][=C][C][=C][C][=C][C][Ring1][=Branch1][=N][Ring1][#Branch2][=C][Ring2][Ring1][C][C][C][=Branch1][C][=O][O]\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given IUPAC, write its lipophilicity. ->\",\n        \"input\": \" 6-[[[1-[2-(6-methoxy-3-oxo-1,4-benzoxazin-4-yl)ethyl]piperidin-4-yl]amino]methyl]-4h-pyrido[2,3-e][1,4]oxazin-3-one\\n\",\n        \"output\": \" 0.87\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SELFIES. ->\",\n        \"input\": \" [O][=C][Branch2][Ring1][C][N][C][=N][C][C][=Branch1][C][=O][N][C][=N][C][=Ring1][#Branch1][S][Ring1][#Branch2][C][=C][C][=C][C][=C][Ring1][=Branch1]\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" Nc1ccc2ncnc(Nc3ccc(F)c(Cl)c3)c2c1\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given IUPAC. ->\",\n        \"input\": \" inventory\\n\",\n        \"output\": \" inventory is not a IUPAC and it does not have lipophilicity.\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given SMILES? ->\",\n        \"input\": \" O=C1N2C=CC=CC2=Nc3ccccc13\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is lipophilicity of given InChI? ->\",\n        \"input\": \" InChI=1S/C16H13NO3S/c18-15-14(21-16(19)17-15)10-11-5-4-8-13(9-11)20-12-6-2-1-3-7-12/h1-9,14H,10H2,(H,17,18,19)\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Write lipophilicity of given SMILES. ->\",\n        \"input\": \" NC(=O)Nc1sc(cc1C(=O)N)c2ccc(OCCN3CCCCC3)cc2\\n\",\n        \"output\": \" 1.2\\n\"\n    }\n]"
  },
  {
    "path": "dataset/chembl/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 24,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('chembl.csv')\\n\",\n    \"# key=csv column name, value=slot in Q\\n\",\n    \"slot = {\\\"smiles\\\":\\\"SMILES\\\", \\\"inchi\\\":\\\"InChI\\\", \\\"selfies\\\":\\\"SELFIES\\\", \\\"iupac\\\":\\\"IUPAC\\\"}\\n\",\n    \"data_list = []\\n\",\n    \"for s in slot.keys():\\n\",\n    \"    for i, element in enumerate(df[s]):\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,2)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What is lipophilicity of given \\\"+ slot[s] + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write lipophilicity of given \\\"+ slot[s] + \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given \\\" + slot[s] + \\\", write its lipophilicity. ->\\\"\\n\",\n    \"        answer = df['lipophilicity'][i]\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] =  element\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(answer)+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 25,\n   \"id\": \"166b1e11\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('../2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 26,\n   \"id\": \"52c48afe\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"7596\\n\",\n      \"253\\n\",\n      \"['mice', 'kite', 'computer', 'visitor', 'pheasant', 'scissors', 'crayon', 'account', 'spring', 'digestion']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"print(len(data_list))\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add = int(len(data_list)/30)\\n\",\n    \"print(add)\\n\",\n    \"add_nouns = random.sample(nouns, add)\\n\",\n    \"print(add_nouns[:10])\\n\",\n    \"for an in add_nouns:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    ran2 = random.sample(list(slot.values()), 1)[0]\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What is lipophilicity of given \\\"+ ran2 + \\\"? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write lipophilicity of given \\\"+ ran2 + \\\". ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given \\\" + ran2 + \\\", write its lipophilicity. ->\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] = an\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" \\\"+an+\\\" is not a \\\"+ran2+\\\" and it does not have lipophilicity.\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\\n\",\n    \"random.shuffle(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 27,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('chembl.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"e77195f1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.6.13\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/matbench_expt_gap/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 1,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('matbench_expt_gap.csv')\\n\",\n    \"slot = {\\\"composition\\\":\\\"composition\\\", \\n\",\n    \"        \\\"band gap\\\":\\\"band gap\\\"}\\n\",\n    \"pair1 = [(\\\"band gap\\\", \\\"composition\\\")]\\n\",\n    \"data_list = []\\n\",\n    \"for df_slice in df.iterrows():\\n\",\n    \"    for p in pair1:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,3)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What is \\\"+ p[0]+\\\" of given \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write \\\"+ p[0]+ \\\" of given \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ p[0] + \\\". ->\\\"\\n\",\n    \"        elif ran == 3:\\n\",\n    \"            question = \\\"Tell me \\\" + p[0] + \\\" of given \\\" + p[1] + \\\". ->\\\"\\n\",\n    \"        elif ran == 4:\\n\",\n    \"            question = \\\"Given \\\" + p[1] + \\\", what is its \\\"+ p[0] + \\\"? ->\\\"\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] = str(df_slice[1][slot[p[1]]])+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(df_slice[1][slot[p[0]]])+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 2,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('matbench_expt_gap.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"ce1a9f8a\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.8.8\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/matbench_expt_gap/matbench_expt_gap.csv",
    "content": "composition,band gap\nAg(AuS)2,0\nAg(W3Br7)2,0\nAg0.5Ge1Pb1.75S4,1.83\nAg0.5Ge1Pb1.75Se4,1.51\nAg2BBr,0\nAg2BiO3,0\nAg2GeS3,1.98\nAg2GeSe3,0.9\nAg2HgI4,2.47\nAg2Mo(I2O7)2,3.06\nAg2P2PbO7,0\nAg2PdO2,0.18\nAg3AsO4,0\nAg3Pd,0\nAg3RuO4,0\nAg5IO6,1.4\nAg7(SI)2,0\nAg7AsS6,1\nAg7AsSe6,1\nAg7NO11,0\nAg8GeS6,1.18\nAg8SnSe6,0.71\nAg9(PbO3)4,0\nAg9Ge2IO8,0\nAgAsSe2,1.4\nAgAu3,0\nAgBi(PS3)2,1.7\nAgBi(PSe3)2,1.4\nAgBiPbS3,1.2\nAgBiPbSe3,0.13\nAgBiS2,0.9\nAgBiSe2,0.34\nAgBr,2.52\nAgCNO,0\nAgCl,5.13\nAgF,2.8\nAgGeO3,0\nAgO,1.57\nAgP15,1.47\nAgPd(IO3)3,1.5\nAgPdO2,0\nAgPt3,0\nAgSO4,0.18\nAgTe2As,0.8\nAl(Ni10B7)2,0\nAl(NiS2)2,0\nAl0.01Cd0.99Sb0.01Te0.99,1.6\nAl0.01Ga0.99P1,2.27\nAl0.01In0.99P1,1.3\nAl0.05Cd0.95Sb0.05Te0.95,1.37\nAl0.15Ga0.85As1,1.6\nAl0.1Cd0.9Sb0.1Te0.9,1.36\nAl0.1In0.9P1,1.5\nAl0.2Ga0.8P1,2.3\nAl0.2In0.8P1,1.7\nAl0.35Ga0.65As1,2\nAl0.3Ga0.7As1,1.81\nAl0.3In0.7P1,1.9\nAl0.45Cd0.55Sb0.45Te0.55,1.93\nAl0.4Cd0.6Sb0.4Te0.6,1.8\nAl0.4Ga0.6P1,2.35\nAl0.4In0.6P1,2.12\nAl0.5Ga0.5As1,2.12\nAl0.6Ga0.4As1,2.3\nAl0.6Ga0.4P1,2.4\nAl0.6In0.4P1,2.3\nAl0.75Ga0.25As1,2.42\nAl0.7In0.3P1,2.3\nAl0.8Ga0.2P1,2.43\nAl0.99Cd0.01Sb0.99Te0.01,2.21\nAl0.99Ga0.01P1,2.49\nAl0.99In0.01P1,2.4\nAl10V,0\nAl13Ru4,0\nAl2(CuSe2)3,0\nAl21Pt8,0\nAl2CoIr,0\nAl2Cr2O7,0\nAl2CrS4,0\nAl2Cu,0\nAl2FeNi,0\nAl2Ru,0\nAl2S3,4.1\nAl2Se3,3.1\nAl3Tc,0\nAl4Cu2O7,0\nAl4Cu9,0\nAl5Rh2,0\nAl6Fe,0\nAl6Ru,0\nAl6Tc,0\nAl7(CN)3,0\nAl9Co2,0\nAl9Ir2,0\nAl9Rh2,0\nAlAgO2,3.6\nAlAgS2,3.13\nAlAgSe2,2.55\nAlAgTe2,1.8\nAlAs,0\nAlB2,0\nAlBi,0.4\nAlCoO3,0\nAlCu3,0\nAlCu7O12,0\nAlCuS2,3.5\nAlCuTe2,2.06\nAlFe2Si,0\nAlFe4(CuO4)3,0\nAlIr,0\nAlNi2,0\nAlPd5I2,0\nAlSn,0\nAlV(TeO4)2,2.9\nAlVCo2,0\nAs2Ir,1\nAs2O3,4\nAs2Os,0.9\nAs2Rh,1.15\nAs2Ru,0.8\nAs2S5,2.48\nAsAu3,0\nAsBr3,2.6\nAsOsS,1.3\nAsP,0.23\nAsPPd,0.45\nAsPPt,0.4\nAsPRu,0.8\nAsPd3Pb2,0\nAsRuS,1.2\nAsS,2.4\nAsS3,2.35\nAsSI,2.05\nAsSeBr,0\nAsSeI,1.76\nAu3S,0\nAuBrO2,0\nB2Mo(PbO2)6,2.9\nB2O3,4.89\nB2Se2O7,4.64\nB3H2Pb2O7.5,4.42\nB3Pb10Br3O13,3.25\nB3Pb3NO10,3.64\nB4C,1.64\nB4H2Pb6O13,3.24\nB4W,0\nB5Mo2,0\nB6As,1.51\nB6P,3.3\nBAs,1.45\nBH(PbO2)2,3.76\nBMo,0\nBP,4.2\nBPb2ClO3,3.99\nBPb6BrO7,2.84\nBPb7Br3O7,2.62\nBRh2,0\nBSb,2.6\nBSbPbS4,1.8\nBSe2Cl,0\nBTe2As,0\nBa(AsPd)2,0\nBa(AsRh)2,0\nBa(BRh)2,0\nBa(FeS2)2,0\nBa(GaS2)2,4.13\nBa(GaSe2)2,3.16\nBa(InS2)2,3.06\nBa(InSe2)2,2.63\nBa(NiP2)2,0\nBa(PdO2)2,0\nBa(SnO2)4,0\nBa(ZnAs)2,0.23\nBa1.88Ta15O32,0.13\nBa12In4S19,2.56\nBa14Ir8(PdO11)3,0\nBa14Na8CaN6,0\nBa23Ga8(SbS19)2,2.84\nBa2B4H2O9,5.12\nBa2B6H4O13,6.53\nBa2B6O11,5.17\nBa2BiSbO6,0\nBa2CaOsO6,0\nBa2CaReO6,0\nBa2Cd(BO2)6,4.59\nBa2Ce2O5,0\nBa2CeInTe5,1.35\nBa2CoWO6,0\nBa2Cu5F14,0\nBa2CuWO6,0\nBa2DyCu3O7,0\nBa2DyGaSe5,2.35\nBa2DyGaTe5,1.13\nBa2DyInSe5,2.27\nBa2DyInTe5,1.35\nBa2ErGaSe5,1.95\nBa2ErGaTe5,1.15\nBa2ErInSe5,2.29\nBa2ErInTe5,1.35\nBa2FeMoO6,0\nBa2FeReO6,0\nBa2Ga8GeS16,3\nBa2Ga8SiS16,3.4\nBa2GaAsSe5,1.39\nBa2GaBiS5,2.38\nBa2GaBiSe5,2.21\nBa2GaBiTe5,1.43\nBa2GaS4,2.55\nBa2GaSbSe5,2.51\nBa2GaSbTe5,1.66\nBa2GaSe4,1.63\nBa2GdGaSe5,1.87\nBa2GdGaTe5,1.12\nBa2GdInSe5,2.24\nBa2GdInTe5,1.36\nBa2HgS5,2.4\nBa2In2S5,2.47\nBa2In2Se5,2.12\nBa2InAgS4,2.32\nBa2InBiS5,1.55\nBa2InSbSe5,1.92\nBa2LaIrO6,0\nBa2LiFe2N3,0\nBa2NaCu3S5,0.45\nBa2NdGaS5,2.12\nBa2NdGaSe5,2.18\nBa2NdInSe5,2.2\nBa2NdInTe5,1.37\nBa2ReNiO6,0\nBa2Sb7HO14,2.7\nBa2ScIrO6,0\nBa2ScTaO6,4.19\nBa2SmCu3O7,0\nBa2SmGaSe5,2.27\nBa2SmGaTe5,1.04\nBa2SmInSe5,2.22\nBa2SmInTe5,1.36\nBa2SmTaO6,3.02\nBa2SnSe4,1.9\nBa2SnSe5,1.8\nBa2TaInO6,4.17\nBa2TbIrO6,0\nBa2ThCu2Se5,1.75\nBa2UCuO6,0\nBa2V2Te2O11,3.16\nBa2V2ZnO8,3.48\nBa2V4(TeO6)3,2.64\nBa2YGaSe5,2.31\nBa2YGaTe5,1.08\nBa2YInSe5,2.31\nBa2YInTe5,1.36\nBa2YReO6,0\nBa2Yb(CuO2)4,0\nBa2Zn0.2B2S5.2,3.54\nBa2ZnSe3,2.75\nBa2ZnTe3,2.1\nBa3(AlGe)2,0\nBa3(LiSn2)4,0\nBa3Ag2(SnS4)2,2.37\nBa3B1.5Sb0.5S6,3.01\nBa3BSbS6,2.62\nBa3BSbSe6,1.89\nBa3Bi0.5B1.5S6,2.43\nBa3Bi2TeO9,2.3\nBa3CaIr2O9,0\nBa3CaRu2O9,0\nBa3Cd(SnS4)2,2.75\nBa3Co10O17,0\nBa3CrS5,0\nBa3Dy2(PS4)4,3.28\nBa3Er2(PS4)4,3.3\nBa3ErRu2O9,0\nBa3Eu(PO4)3,4.09\nBa3FeS4Br,1.65\nBa3Gd2(PS4)4,3.41\nBa3GeS5,3\nBa3Ho2(PS4)4,3.3\nBa3In2(PO4)4,3.87\nBa3InS4Cl,3.42\nBa3La3(Cu3O7)2,1.8\nBa3MgTa2O9,4.28\nBa3N2,0\nBa3NaIr2O9,0\nBa3NaIrO6,0\nBa3Nb2CoO9,0\nBa3Nb2Se9,1.3\nBa3P3ClO10,6.89\nBa3PN,0\nBa3Sb2S7,2.4\nBa3Sn(SbSe4)2,0.97\nBa3Sn0.87Bi2.13Se8,0.79\nBa3Ta2Se9,1.6\nBa3Ta2ZnO9,4.32\nBa3Ta5NO14,2.8\nBa3Tb2(PS4)4,3.37\nBa3Te,0\nBa3ThSe7,1.96\nBa3V2(SeO4)4,2.87\nBa3YIr2O9,0\nBa3Yb4O9,0\nBa3ZrRu2O9,0\nBa4B11O20F,7.1\nBa4Ga4GeSe12,2.18\nBa4Ga4SnSe12,2.16\nBa4Ga5AgS12,2.52\nBa4Ga5CuS12,2.82\nBa4Ga5CuSe12,1.45\nBa4Ga5Si18,0.31\nBa4Ge3S9Cl2,2.91\nBa4Ge3Se9Cl2,1.89\nBa4InAgSe6,2.41\nBa4InCuSe6,2.23\nBa4LiGa5Se12,2.65\nBa4Nb14O23,0\nBa4Sb3S8Cl,2.09\nBa4Si20Au3,0\nBa4Si3Se9Cl2,1.76\nBa4Sm2Cu2O9,0\nBa4Yb(CuO3)3,0\nBa5(Ga2Se5)2,2.2\nBa5(GaSe4)2,2.51\nBa5Al2Ge7,0\nBa5Bi3,0\nBa5Cd(Ga2Se5)3,2.6\nBa5Ga6GeP12,1.39\nBa5Ga6SnP12,1.21\nBa5Ge3,0\nBa5In4Bi5,0\nBa5In4Te4S7,2.13\nBa5Sb3,0\nBa5V3O12F,3.85\nBa6Al4B14O33,3.44\nBa6Ga2SnSe11,1.99\nBa6In2NF,0\nBa6Sn6Se13,1.52\nBa7(SnS3)5,2.29\nBa7B3O9F5,4.94\nBa7Ga5AgS15,2.6\nBa7Ru4Br2O15,0\nBa8Al10B12O41,3.1\nBa8Hg4Se7S5,1.98\nBa8Sn4S15,2.31\nBa8Ta7O24,0\nBaAg,0\nBaAg2,0\nBaAgSbS3,2.2\nBaAl2,0\nBaAl4Se7,3.4\nBaAlCu4O7,0\nBaAu(IO3)5,2.32\nBaAu2,0\nBaB6,2.64\nBaBClF4,6.89\nBaBSbS4,2.34\nBaBiClO2,3.71\nBaCaB2O5,5.6\nBaCaSn3,0\nBaCdSnS4,2.3\nBaCu2SnSe4,0.48\nBaCuSbS3,2\nBaCuSbSe3,1.6\nBaCuTeF,2.3\nBaDy2CuO5,0\nBaEu2Mn2O7,0\nBaGa2GeS6,3.23\nBaGa2SiS6,3.75\nBaGa2SiSe6,2.88\nBaGa4S7,3.54\nBaGa4Se7,2.64\nBaGe2,1\nBaGe3Pt,0\nBaGe4(IrS3)2,1.54\nBaGe4(IrSe3)2,1.33\nBaGe4(RhSe3)2,1.09\nBaHgS2,1.93\nBaHgSe2,1.56\nBaIn2(P2O7)2,3.97\nBaIn2Ir,0\nBaLa2CoS5,0\nBaLa2In2S7,1.87\nBaLa2In2Se7,1.66\nBaLa2Te5O14,3.81\nBaLi4,0\nBaMn4O7,0\nBaMn4ZnO8,0\nBaMnO3,0\nBaNa2GeS4,3.7\nBaNa2GeSe4,2.25\nBaNa2SnS4,3.27\nBaNa2SnSe4,2.46\nBaNaB5O9,4.78\nBaNb4O6,0\nBaO,4.8\nBaPd(IO3)4,1.97\nBaPdSe6,2.15\nBaPrO3,2\nBaPt5,0\nBaReH9,3.44\nBaS,3.88\nBaSi,0\nBaSi2,1.3\nBaSn2S5,2.35\nBaSn3,0\nBaSnO3,3.1\nBaTaNO2,1.78\nBaTbMn2O6,0\nBaTe,3.4\nBaTeMo2O9,3.12\nBaTh3,0\nBaTi14O28,0\nBaTi4O7,0\nBaTi4O8,0\nBaTl(MoO3)2,0\nBaTl3,0\nBaUSe3,1\nBaV2SeO8,2.13\nBaYb2O4,0\nBaYbSn3,0\nBaZn(MoO2)4,0\nBaZn5,0\nBaZnGeSe4,2.46\nBaZnSO,3.9\nBaZnSiSe4,2.71\nBe12Pt,0\nBe22Re,0\nBe2HgTe,0\nBe2W,0\nBe3N2,3.8\nBe3Sb2,0.67\nBeAlB,0\nBeCu,0\nBeFe2Si,0\nBeGaO3,0\nBeGaRh2,0\nBeO,10.39\nBePd2,0\nBePd3,0\nBeS,4.17\nBeSe,4\nBeSiOs2,0\nBeSiRu2,0\nBeTcSe,0\nBeTe,2.89\nBi0.002Te0.003Pb0.999Se0.999,0.79\nBi0.04Te0.06Pb0.98Se0.98,0.28\nBi0.2Sb1.8Te3,0.28\nBi0.2Te0.3Pb0.9Se0.9,0.25\nBi0.4Sb1.6Te3,0.21\nBi0.4Te0.6Pb0.8Se0.8,0.22\nBi0.6Sb1.4Te3,0.2\nBi1.4Sb0.6Te3,0.17\nBi1.6Sb0.4Te3,0.16\nBi1.8Sb0.2Te3,0.15\nBi1.98Sb0.02Te3,0.14\nBi12PO20,3.25\nBi12Rh12O41,0\nBi1Sb0.15,0.02\nBi2(BO3)3,0\nBi2(MoO4)3,2.9\nBi2(PO4)3,0\nBi24BO39,2.91\nBi2AsClO4,3.43\nBi2CO5,3.42\nBi2I4O13,3.3\nBi2Mo2Se2O13,3.15\nBi2O5,0\nBi2Pd3S2,0\nBi2Pt,0\nBi2SI2O11,3.74\nBi2Se3,0.35\nBi2SeI2O11,3.7\nBi2Te0.03Se2.97,0.27\nBi2Te0.1Se2.9,0.78\nBi2Te0.3Se2.7,0.24\nBi2Te0.45Se2.55,0.2\nBi2Te0.4Se2.6,0.7\nBi2Te0.6Se2.4,0.28\nBi2Te0.9Se2.1,0.28\nBi2Te1.2Se1.8,0.28\nBi2Te1.5Se1.5,0.29\nBi2Te2.1Se0.9,0.29\nBi2Te2.4Se0.6,0.25\nBi2Te2.7Se0.3,0.2\nBi2Te2.97Se0.03,0.15\nBi2Te2SO10,3.6\nBi2Te2Se,0.3\nBi2Te3,0.25\nBi3BTeO9,2.6\nBi3I4O13F3,3.7\nBi3Se2NO11,3.59\nBi4I,0\nBi4Pb7Se13,0.29\nBi4Pd(SeO3)4,2.06\nBi5IO7,2.76\nBi7O5F11,4.05\nBi8Te7S5,0.4\nBi9S6O7.5,1.27\nBiAs2Os,0\nBiBPbO4,3.2\nBiBr3,2.66\nBiBrO,2.92\nBiClO,3.46\nBiIO3F2,3.97\nBiO,0\nBiP3(PbO4)3,3.7\nBiPO4,3.85\nBiPb2S2I3,1.6\nBiPbClO2,2.45\nBiPd,0\nBiSBr,1.88\nBiSCl,1.89\nBiSI,1.56\nBiSbTe3,0.19\nBiSe,0.4\nBiSeI,1.28\nBiSeO3F,3.83\nBiTeI,0.46\nBiTeNO6,3.62\nCBr4,3.7\nCI4,2.26\nCa(AgGe)2,0\nCa(Al4Co)2,0\nCa(AlZn)2,0\nCa(BC)2,0\nCa(BIr)2,0\nCa(BiO2)2,3.08\nCa(CoGe)2,0\nCa(CoS2)4,0\nCa(GdS2)2,2.55\nCa(GeRh)2,0\nCa(LaS2)2,2.7\nCa(MnAs)2,0\nCa(NdS2)2,2.7\nCa(Ni2O3)2,0\nCa(PrS2)2,2.9\nCa(SiPd)2,0\nCa(SmS2)2,2.05\nCa(TiS2)4,0\nCa10Ge16(B2O17)3,5.47\nCa11Bi10,0\nCa11Ga7,0\nCa2Bi2O5,3.34\nCa2CdAs2,0.95\nCa2CdPb,0\nCa2Co9O13,0\nCa2CuWO6,0\nCa2Ge,1\nCa2GeN2,0\nCa2Mn9O13,0\nCa2MnAlO5,0\nCa2NiIrO6,0\nCa2Os2O7,0\nCa2PbAu2,0\nCa2ScSbO6,3.68\nCa2Si,1.9\nCa2SmTaO6,3.45\nCa2Sn,0.9\nCa2Sn2F3,0\nCa2SnS4,2.32\nCa2Ti9O13,0\nCa2TlCd,0\nCa2ZnRh,0\nCa3(GaPt)2,0\nCa3Al2Ge3,0\nCa3Au,0\nCa3Au4,0\nCa3Bi(PO4)3,4.2\nCa3BiAs,0\nCa3BiSb,0\nCa3Cu2(ClO2)2,0\nCa3In,0\nCa3La2(SnS4)3,1.45\nCa3N2,1.55\nCa3PbN,0\nCa3Sb2,1.4\nCa3SbN,0\nCa3Sn2S7,0\nCa3Ti2(SiO4)3,1.65\nCa3TlN,0\nCa3Zr17O37,0\nCa4Al3O10,0\nCa4Bi6O13,2.76\nCa5(Bi7O13)2,2.6\nCa5Au2,0\nCa5B3O9F,6.53\nCa5Ir,0\nCa5Sb3,0\nCa5Sn4S13,0\nCa6Ag16N,0\nCa6Cu2Sn7,0\nCaAgF5,0\nCaAu5,0\nCaB6,4.5\nCaCdPd2,0\nCaCdSi,0\nCaCu5,0\nCaEu2O3,0\nCaEuO2,0\nCaF2,9.92\nCaGa3Ni2,0\nCaGaAu3,0\nCaGaGe,0\nCaGe2,0\nCaHfZn,0\nCaHg2,0\nCaI2,5.98\nCaIn2Ir,0\nCaIn4Ir,0\nCaInAu,0\nCaInPt,0\nCaIrO3,0\nCaMg2N2,3.25\nCaMgSn,0\nCaMnSn,0\nCaNi5,0\nCaOsO3,0\nCaPb,0\nCaPd3C,0\nCaPrZn2,0\nCaSnO3,4.4\nCaTaNO2,2.4\nCaTi4O8,0\nCaTiO2,0\nCaVO2,0\nCaYbInSe4,0\nCaZn2,0\nCaZn3,0\nCaZn3Ni2,0\nCaZn5,0\nCaZnSO,3.7\nCd(GaS2)2,3.4\nCd(In15Te23)2,1.17\nCd(PS2)2,3.76\nCd0.01Ga0.99Sb0.99Te0.01,0.72\nCd0.01Hg0.99Se1,1.72\nCd0.01In0.99Te0.01As0.99,0.76\nCd0.02In0.98Te0.02As0.98,0.73\nCd0.03In0.97Te0.03As0.97,0.71\nCd0.04In0.96Te0.04As0.96,0.69\nCd0.05Ga0.95Sb0.95Te0.05,0.74\nCd0.05In0.95Te0.05As0.95,0.68\nCd0.06In0.94Te0.06As0.94,0.68\nCd0.07In0.93Te0.07As0.93,0.68\nCd0.1Ga0.9Sb0.9Te0.1,0.78\nCd0.1In0.9Te0.1As0.9,0.69\nCd0.204Hg0.796Te1,0.06\nCd0.23Hg0.77Te1,0.12\nCd0.28Hg0.72Te1,0.21\nCd0.2Ga0.8Sb0.8Te0.2,0.8\nCd0.2In2.4Ag0.4Te4,0.42\nCd0.35Hg0.65Te1,0.28\nCd0.37Hg0.63Te1,0.35\nCd0.3Hg0.7Se1,1.1\nCd0.3Hg0.7Te1,0.27\nCd0.4Hg0.6Se1,0.95\nCd0.5Hg0.5Se1,0.8\nCd0.5In2.25Ag0.25Te4,0.39\nCd0.5In2.2Ag0.4Te4,0.19\nCd0.6Hg0.4Se1,0.7\nCd0.75In2.1Ag0.2Te4,0.54\nCd0.7Hg0.3Se1,0.55\nCd0.8Hg0.2Se1,0.45\nCd0.8In2.1Ag0.1Te4,0.29\nCd0.99Ga0.01Sb0.01Te0.99,1.35\nCd0.99Hg0.01Se1,0.29\nCd0.9Hg0.1Se1,0.35\nCd12Ge17(B4O29)2,4.29\nCd13I28,0\nCd1Se0.01S0.99,2.4\nCd1Se0.2S0.8,2.23\nCd1Se0.35S0.65,2.13\nCd1Se0.45S0.55,2.05\nCd1Se0.65S0.35,1.93\nCd1Se0.99S0.01,1.68\nCd2AgRh,0\nCd2InAgTe3,0.47\nCd2InCuTe3,0.7\nCd2InCuTe4,0.85\nCd2PbO4,0\nCd3AgPS6,2.56\nCd3Bi(PO4)3,3.9\nCd3Bi2,0.2\nCd3In2(Te2S)2,1.23\nCd3P2,0.5\nCd3Sb2,0.3\nCd3Te2MoO10,3.81\nCd4P2Br3,2.19\nCd4P2Cl3,2.17\nCd4P2I3,2.17\nCd4Sb2I3,1.83\nCd4Sb3,1.25\nCd5Ga2(Te3S)2,1.29\nCd6P7,0.85\nCd8B5O15F,3.14\nCdAg,0\nCdAg2(PS3)2,2.49\nCdAg2GeS4,2.32\nCdAsPd5,0\nCdAuO2,0\nCdBiClO2,3.08\nCdBr2,4.47\nCdCl2,5.7\nCdCu(SeO3)2,3.33\nCdCu2GeS4,2.05\nCdCu2GeSe4,1.2\nCdCu2SnS4,1.37\nCdCu2SnSe4,0.96\nCdF2,6\nCdHIO4,4.35\nCdHg4(AsI2)2,1.45\nCdHg6(As2Br3)2,1.89\nCdI2,3.8\nCdIClO3,4.3\nCdIn,0.6\nCdIn8Te13,1.02\nCdInCuSe3,1.66\nCdO,2.3\nCdP4PbO12,4.85\nCdPd,0\nCdPt,0\nCdRhF6,0\nCdSb2Se3Br2,1.4\nCdSb4MoO10,3.4\nCdSnO3,3\nCe(AlZn)2,0\nCe(BC)2,0\nCe(CoAs)2,0\nCe(CoB)4,0\nCe(CuSb)2,0\nCe(HO)3,0\nCe(InS2)3,1.11\nCe(MnGe)2,0\nCe(MnSi)2,0\nCe(PPt2)2,0\nCe(SiAu)2,0\nCe(SiNi)2,0\nCe(SiPd)2,0\nCe1.3Lu0.7S3,1.25\nCe10Se14O,1.93\nCe15B8N25,3.5\nCe1Mn0.5Se1O1,2.01\nCe2(SbPd3)3,0\nCe2(SnSe3)3,0.3\nCe2Al2Co15,0\nCe2Co5B2,0\nCe2CrN3,0\nCe2Cu(NO)2,0\nCe2Fe(SeO)2,0.64\nCe2Fe17,0\nCe2Ge2Se7,1.1\nCe2GeSe5,1.7\nCe2S2O,0\nCe2S3,1.12\nCe2Sb,0\nCe2Se3,1.75\nCe2SiSeO4,0\nCe2Ti2O7,0\nCe2ZnNi2,0\nCe3(Al3Ru)4,0\nCe3Al,0\nCe3AlC,0\nCe3B2(ClO2)3,0\nCe3In3Ru2,0\nCe3LuSe6,1.1\nCe3MnAlS7,0\nCe3MoO7,2\nCe3NbS3O4,0\nCe3Pd5,0\nCe3SiPt5,0\nCe3Ta(ClO2)3,0\nCe3TaO7,0\nCe4(GeS4)3,2.3\nCe4Bi3,0\nCe4FeSe6O,0\nCe4InSbSe9,1.69\nCe4Si3Rh4,0\nCe4Te7,0.5\nCe5(SiN3)3,0\nCe5CuSe8,0\nCe5Ge3,0\nCe5Si3,0\nCe6B2(CBr)3,0\nCe8Sb2S15,1.99\nCe8U2O21,0\nCe9SmO20,0\nCeAgSn,0\nCeAl2Pd5,0\nCeAl2Pt3,0\nCeAl3Ni2,0\nCeAlO3,0\nCeAlSi2,0\nCeAsPd,0\nCeAsSe,0\nCeB2Ir3,0\nCeBC,0\nCeBiW2O9,2.34\nCeCd2Ag,0\nCeCdAu2,0\nCeCoGeH,0\nCeF3,4.85\nCeGaO3,0\nCeHSe,0\nCeHg,0\nCeInIr,0\nCeIr5,0\nCeLu3,0\nCeMg2Ag,0\nCeMgAg2,0\nCeMgNi4,0\nCeMgPt,0\nCeMgZn2,0\nCeMoO4F,2.52\nCeN,0.7\nCeNbO4,0\nCeO2,3.41\nCeOs2,0\nCePd5,0\nCePrO2,0\nCeRh,0\nCeSI,0\nCeSbO3,0\nCeScO3,3.2\nCeSi2Ni,0\nCeSi2Pt,0\nCeSiI,0\nCeSiIr,0\nCeSiOs,0\nCeTaN2O,1.9\nCeTl2P2S7,2.4\nCeTl3,0\nCeTlZn,0\nCeZnPO,0\nCo(PO3)4,0\nCo(WO4)2,0\nCo1Te1.88,0.2\nCo2B4Mo,0\nCo2Ge,0\nCo2O3,0\nCo2Te3O8,3.6\nCo3H,0\nCo3Se4,0\nCo3W,0\nCo5Ge7,0\nCo5RuO8,0\nCo7Mo6,0\nCo7Re17O48,0\nCoAs3,0.4\nCoAsRh,0\nCoAsS,0.6\nCoAsSe,0.2\nCoCu2Sn,0\nCoGe,0\nCoH2(SN)4,0\nCoMoP2,0\nCoN,0\nCoOF,0\nCoP2,0.35\nCoP3,0.45\nCoPS,0.4\nCoSb2,0.17\nCoSb3,0.49\nCr(FeSe2)2,0\nCr(MoS2)2,0\nCr10Sb3Te7,0\nCr2CuS4,0\nCr2CuTe4,0\nCr2GeC,0\nCr2HO4,0\nCr2HgSe4,0\nCr2NiS4,0\nCr2O3,3.4\nCr2P3O11,0\nCr2SbTe,0\nCr3N2,0\nCr3Ni(PO4)6,0\nCr3P,0\nCr3Se4,1.59\nCr4As3,0\nCr4Cu3Te8,0\nCr7C3,0\nCrAs,0\nCrB2(PbO2)6,1.8\nCrBi2I2O11,2.4\nCrCo2Bi,0\nCrCoGe,0\nCrCoPt2,0\nCrCu2Si,0\nCrFe2Sb,0\nCrFeP,0\nCrH9(CN2)3,0\nCrIrO4,0\nCrIrO6,0\nCrNi3,0\nCrNiAs,0\nCrNiP2O9,0\nCrO2,0.23\nCrO3,1.4\nCrPbO4,2.25\nCrSb2,0.14\nCrSi2,1.3\nCrTe2,0.17\nCs(AsRu)2,0\nCs(MoO3)3,0\nCs0.4K0.6P1Se6,2.1\nCs1.13Cd1.13Bi2.87Se6,1\nCs1.43Cd1.43Bi2.57S6,1.28\nCs10Cd4Sn4S17,3.16\nCs2AgBiBr6,2.19\nCs2AgBiCl6,2.77\nCs2Al2B2O7,4.13\nCs2Ba3(P2O7)2,6.31\nCs2Cd(PSe3)2,2.63\nCs2Cd0.25Hg5.75S7,1.66\nCs2Cd1.35Hg4.65S7,1.84\nCs2Cd2Bi2S5,1.7\nCs2Cd3(B4O7)4,4.76\nCs2Cd3Te4,2.48\nCs2CrCl4,0\nCs2Cu(PS3)3,2.4\nCs2Cu2Sb2S5,1.6\nCs2DyCu3Te4,1.38\nCs2Ga2S5,3.26\nCs2Ga2Se5,1.95\nCs2Hg(ICl)2,2.15\nCs2Hg3I8,2.56\nCs2Hg3S4,2.8\nCs2Hg6S7,1.63\nCs2La1.19Bi8.81S16,1\nCs2Li3(BO2)5,7.3\nCs2MgGe3Se8,2.04\nCs2MgSn3Se8,1.92\nCs2Mo15S19,0\nCs2NaCoF6,0\nCs2NaMgF6,0\nCs2NaMnF6,0\nCs2NbCuSe4,2.19\nCs2P2PdSe6,1.6\nCs2PdSe8,1.5\nCs2Pt(IO3)6,2.4\nCs2SCl6F,0\nCs2Sb,0.62\nCs2SeClF6,0\nCs2SiB4O9,6.53\nCs2Sn(PSe3)2,2.06\nCs2Sn3(SbS5)2,2.34\nCs2Te,3.5\nCs2TeBr6,2.12\nCs2TeI6,1.5\nCs2Th(PS3)3,2.8\nCs2Ti(AgS2)2,2.44\nCs2VAgS4,1.77\nCs2Zn3(SeO3)4,4.3\nCs2ZnGe3S8,3.33\nCs2ZnGe3Se8,2.31\nCs2ZnGe3Te8,1.07\nCs2ZnSn3Se8,2.12\nCs39Ga53(Se16Cl)6,2.74\nCs3As,0.6\nCs3Bi2Br9,2.5\nCs3Bi2I9,1.8\nCs3Li4(BO2)7,6.53\nCs3NaZn2Ge21,0.3\nCs3Nb2AsSe11,1.35\nCs3Nb9(TeO8)4,3.22\nCs3PW3O13,3.27\nCs3Sb,1.6\nCs3Sb2Br9,2.3\nCs3Sb2I9,1.89\nCs3Sn3Cl7F2,2.96\nCs3V2Cl9,0\nCs4Ag9(SbS3)4,2\nCs4BiAs3Se7,1.02\nCs4Ga4Si19,1.14\nCs4Ge(PSe3)4,2\nCs4Ge5(PbS4)4,1.95\nCs4In8GeSe16,2.2\nCs4Zr3S14,2.35\nCs5Bi(PSe3)4,1.85\nCs5Mo21Se23,0\nCs5P5Se12,2.17\nCs6.4Na1.6Ga8Ge38,0.22\nCsAg2AsS3,2.7\nCsAg2TeS6,2.04\nCsAg5Te3,0.65\nCsAgCl3,0\nCsAgSb4S7,2.04\nCsAu,2.3\nCsB3O5,7.42\nCsBi2,0.55\nCsBi3Se5,0.43\nCsBiS2,1.39\nCsBiSe2,1.07\nCsCaO3,0\nCsCd4Ga5S12,3.09\nCsCd4Ga5Se12,2.21\nCsCd4Ga5Te12,1.67\nCsCd4In5Se12,1.62\nCsCd4In5Te12,1.42\nCsCdBO3,2.58\nCsCdInSe3,2.4\nCsCeCdSe3,2.4\nCsCeHgSe3,1.94\nCsCu(SbS2)2,1.7\nCsCu2AsS3,2.3\nCsCu2SbS3,1.63\nCsDy9(Cd2Se9)2,1.99\nCsEr9(Cd2Se9)2,2.09\nCsErZnSe3,2.56\nCsEuF3,0\nCsF,10\nCsGa(SnSe3)2,1.87\nCsGa7,0\nCsGaS3,3\nCsGaSnSe4,1.97\nCsGdO3,0\nCsGdZnTe3,2.13\nCsGe5BO12,4.89\nCsGeB3O7,5.76\nCsGeI3,1.6\nCsH3(SeO3)2,4.77\nCsHo9(Cd2Se9)2,2.06\nCsIn(SnSe3)2,1.78\nCsInGeSe4,2.32\nCsInHgS3,2.3\nCsInI3,0\nCsInS2,3.4\nCsInSe2,2.81\nCsInSnS4,2.9\nCsInTe2,2.16\nCsInTe3O8,3.9\nCsIr,0\nCsIrO3,0\nCsK(PSe4)2,2.36\nCsLaHgSe3,2.46\nCsLi(B3O5)2,6.89\nCsLiCO3,6.19\nCsLu7S11,1.86\nCsLu7Se11,1.78\nCsMg149,0\nCsMn4Ga5Te12,1.55\nCsMn4In5Se12,1.79\nCsMn4In5Te12,1.48\nCsMnSb,0\nCsNa2Sb,0.8\nCsNa8(B7O12)3,4.67\nCsNb6I11,0\nCsNbSe2O7,4.2\nCsNi2F6,0\nCsPPbO4,4.39\nCsPSe4,2.44\nCsPSe6,1.9\nCsRb(PSe4)2,2.41\nCsRb2Sb,1.5\nCsRbP,0\nCsSb(SO4)2,4.68\nCsSbS2,2.8\nCsSbSe2,1.7\nCsSbTe2,0.43\nCsSc(SeO3)2,5.2\nCsScBr3,0\nCsSmCdSe3,2.45\nCsSmHgSe3,2.37\nCsSn3,0\nCsTa3(SeO6)2,3.88\nCsTaPSe6,2.29\nCsTb9(Cd2Se9)2,1.95\nCsTbZnTe3,2.12\nCsTiCl3,0\nCsTiF4,0\nCsTm9(Cd2Se9)2,2.16\nCsUCuS3,0\nCsVP2S7,0\nCsWCl6,0\nCsYCdSe3,2.54\nCsYHgSe3,2.54\nCsYTe3O8,3.4\nCsYbCoSe3,0.95\nCsYbMnSe3,1.59\nCsZn2B3O7,5.69\nCsZn4In5Se12,1.61\nCsZn4In5Te12,1.61\nCsZrPSe6,2\nCu(IrS2)2,0\nCu(NO3)2,0\nCu0.5Ge1Pb1.75S4,1.48\nCu0.96Bi2Se3I1,0.68\nCu1.8S1,2.3\nCu10Sb3,0\nCu11Sb4S13,0\nCu15Si4,0\nCu18S11,0\nCu23(Sb4S13)2,0\nCu25Se26,0\nCu2GeS3,0.53\nCu2H3ClO3,0\nCu2Hg2SF6,0\nCu2HgGeSe4,0\nCu2O,2.58\nCu2OF2,0\nCu2PHO5,0\nCu2Sb,0\nCu2Te3O8,2.64\nCu2WSe4,1.65\nCu3(BiI4)4,0\nCu3(P2O7)2,0\nCu3Bi6S10I,0.72\nCu3Hg2(Te3O8)2,2.56\nCu3Pd,0\nCu3SbSe4,0.31\nCu3Se2(ClO3)2,0\nCu4As2O9,0\nCu4H10SO12,0\nCu4Pd,0\nCu4Sn7S16,0.8\nCu4W(SCl)4,0\nCu5(Si2O7)2,0\nCu6PbO8,0\nCu7Hg6,0\nCu8O,0\nCu9O13,0\nCu9S5,0\nCu9Se4(Cl3O7)2,0\nCuBS2,3.61\nCuBi(PSe3)2,1.2\nCuBiPbS3,0.12\nCuBiPbSe3,0.07\nCuBiSO,1.07\nCuBiSeO,0.82\nCuCN2,0\nCuClO2,0\nCuF,0\nCuHg(SeO3)2,3.25\nCuMoO4,0\nCuN3,4.17\nCuNi(CN)4,2.7\nCuP2(HO3)2,0\nCuPO4F,0\nCuPS3,2.2\nCuPd,0\nCuPtO2,0\nCuSbPbS3,1.31\nCuSbS2,1.38\nCuSbSe2,1.05\nCuSeO3,0\nDy(Al2Cu)4,0\nDy(CoGe)2,0\nDy(CuSe)3,0.2\nDy(CuSi)2,0\nDy(CuTe)3,0.34\nDy(GeRu)2,0\nDy(InS2)3,1.22\nDy12C6I17,0\nDy12Co7,0\nDy1Te1.4,0.6\nDy1Te1.45,0.6\nDy1Te1.7,0.35\nDy2(GePt3)3,0\nDy2(MoO4)3,1.92\nDy2AlCo2,0\nDy2C,0\nDy2CdPd2,0\nDy2CuOs,0\nDy2MgIn,0\nDy2MgTl,0\nDy2Ni12P7,0\nDy2O3,5\nDy2S3,2.91\nDy2Sn5,0\nDy2Te3,0.69\nDy2Ti3Si4,0\nDy2TlCd,0\nDy2ZnIn,0\nDy3(CuGe)4,0\nDy3Al0.5Si1S7,2.22\nDy3Ga,0\nDy3GaS6,2.81\nDy3InC,0\nDy3MnB7,0\nDy4CdRh,0\nDy4GaSbS9,2.58\nDy4Sb3,0\nDy4Te3S4,1.43\nDy5Pb3,0\nDy5Sn3,0\nDy6FeTe2,0\nDy7In(CoGe3)4,0\nDyAg,0\nDyAgGe,0\nDyAgHg2,0\nDyAs,1\nDyB2Rh2C,0\nDyB6,3.3\nDyBPd3,0\nDyBiPd,0\nDyBiPt,0\nDyCd2,0\nDyCoSi2,0\nDyFeSi,0\nDyGe,0\nDyInAu,0\nDyInCu2,0\nDyInPt2,0\nDyIr2,0\nDyMn2,0\nDyNiGe2,0\nDyNiSn,0\nDyPO4,6.38\nDyRh,0\nDyS2,0\nDySiIr,0\nDySn3,0\nDySnRu2,0\nDyYAg2,0\nDyZnGa,0\nDyZnRh2,0\nDyZrRu2,0\nDyZrSb,0\nEr(Al10Cr)2,0\nEr(CrSi)2,0\nEr(CuGe)2,0\nEr(CuTe)3,0.24\nEr(InS2)3,1.28\nEr(ReO4)2,0\nEr(SiPd)2,0\nEr2(Ga3Co)3,0\nEr2(MoO4)3,0.96\nEr2C3,0\nEr2Fe14B,0\nEr2Mg3Ru,0\nEr2MnC4,0\nEr2O3,5.42\nEr2Se3,1.66\nEr2SnAu2,0\nEr2Te3,0.9\nEr3Al3NiGe2,0\nEr3SnC,0\nEr3Te4,0.9\nEr4NiB13,0\nEr5Bi3,0\nEr5NiPb3,0\nEr5Si3,0\nEr6MnBi2,0\nErAgSn,0\nErAl9(Fe2Si3)2,0\nErAlGe,0\nErB2Ir3,0\nErB2Ru3,0\nErB6,3.5\nErBPd3,0\nErBiW2O9,3.26\nErCu,0\nErCuPb,0\nErFeC2,0\nErHg2,0\nErLu3,0\nErMg2,0\nErNi4Au,0\nErNi4B,0\nErNiSn,0\nErPbAu,0\nErRu3,0\nErSe2,1.07\nErSiPd,0\nErSnAu,0\nErTe,0.9\nErTlPd,0\nErZn12,0\nEu(AlAu)2,0\nEu(AsPd)2,0\nEu(BiSe2)2,1.02\nEu(BiTe2)2,0.44\nEu(CdSb)2,0\nEu(ClO4)3,0\nEu(DySe2)2,1.8\nEu(ErSe2)2,1.7\nEu(FeSi)2,0\nEu(GaS2)2,2.25\nEu(GaSe2)2,2.16\nEu(GaTe2)2,1.7\nEu(HoSe2)2,1.8\nEu(InAs)2,0\nEu(InS2)2,1.5\nEu(InSe2)2,1.31\nEu(InTe2)2,1.22\nEu(LuSe2)2,1.7\nEu(MgBi)2,0\nEu(MnGe)2,0\nEu(Ni2B)6,0\nEu(NiAs)2,0\nEu(POs)2,0\nEu(SbS2)2,1.2\nEu(SbSe2)2,0.95\nEu(TmSe2)2,1.8\nEu(ZnGe)2,0\nEu(ZnSi)2,0\nEu1.75Ag0.5Ge1S4,2.14\nEu1.83Ta15O32,0.23\nEu2(Ga3Rh)3,0\nEu2C(NO)2,0\nEu2CuO4,0\nEu2Ga2GeS7,2.3\nEu2Ge(BO4)2,0\nEu2O3,4.5\nEu2PBr,0\nEu2ReO5,0\nEu2Se3,1.02\nEu2SnSe5,1.07\nEu2TeO2,0\nEu3(InP2)2,0.45\nEu3As2,0.6\nEu3BWO9,0\nEu3Bi4S9,1.18\nEu3P2,1.2\nEu3S4,1.7\nEu3Sb4S9,1.2\nEu3Sb4Se9,1.08\nEu3Se4,0.58\nEu3Sn,0\nEu4Te7,0.31\nEu7(Ga3Sb4)2,0.6\nEuAgSb,0\nEuAl2O4,2.74\nEuAlO3,0\nEuB(SbO4)2,3.46\nEuBi3,0\nEuBiW2O9,3.63\nEuCd11,0\nEuClO,0\nEuCo8P5,0\nEuCu2SnS4,1.85\nEuCu9Sn4,0\nEuCuSeF,0\nEuCuSeO,0\nEuF3,0\nEuGe3Pt,0\nEuH2,1.85\nEuIn2(GeIr)4,0.26\nEuN,1.25\nEuNiGe3,0\nEuO,1.12\nEuPPt,0\nEuPd,0\nEuRhO3,0\nEuS,1.65\nEuSb4S7,0.98\nEuSb4Te7,0.54\nEuSbO3,0\nEuScO3,0\nEuSe,3.1\nEuSeClO3,0\nEuSn3,0\nEuSnAu2,0\nEuSnO3,0\nEuSnTe2,0.6\nEuTiClO3,0\nEuTiO3,0\nEuTl,0\nEuZn,0\nFe(PdSe)2,0\nFe10O9F11,0\nFe12As5,0\nFe2B(PO4)3,3.52\nFe2Cu(PO4)3,0\nFe2O2F3,0\nFe2O3,2.2\nFe2S,0\nFe3B,0\nFe3N,0\nFe3Si,0\nFe4H15(IO8)3,2.3\nFe4O7F,0\nFe4Si2Sn7O16,0\nFe6O7F5,0\nFe6W6C,0\nFe9Co7,0\nFeAg3(CN)6,0\nFeAgSe2,0.23\nFeAs2O7,0\nFeAsSe,0.6\nFeBi(SeO3)3,2.54\nFeBi25O39,2.8\nFeCo2Si,0\nFeCoAs,0\nFeCuSe2,0.15\nFeCuTe2,0.16\nFeI2,5.15\nFeOF,0\nFeP,0\nFeP4,0.32\nFePS,0.25\nFePd3,0\nFeRhO3,0\nFeSn,0\nGa1As0.1P0.9,1.22\nGa0.001Te1Pb0.999,0.3\nGa0.005Te1Pb0.995,0.37\nGa0.01Te1Pb0.99,0.42\nGa0.04Te1Pb0.96,0.37\nGa0.07Te1Pb0.93,0.34\nGa0.95Hg0.05Sb0.95Te0.05,0.69\nGa0.99Hg0.01Sb0.99Te0.01,0.72\nGa0.9Hg0.1Sb0.9Te0.1,0.65\nGa1.001Sb0.999Se0.003,0.71\nGa1.001Sb0.999Te0.003,0.72\nGa1.002Sb0.998Se0.006,0.7\nGa1.002Sb0.998Te0.006,0.7\nGa1.005Sb0.995Se0.015,0.64\nGa1.005Sb0.995Te0.015,0.68\nGa1.01Cu0.99Se2.01,1.59\nGa1.01Sb0.99Se0.03,0.62\nGa1.01Sb0.99Te0.03,0.68\nGa1.02Sb0.98Se0.06,0.63\nGa1.02Sb0.98Te0.06,0.68\nGa1.05Sb0.95Se0.15,0.66\nGa1.05Sb0.95Te0.15,0.68\nGa1.1Cu0.9Se2.1,1.59\nGa1.1Sb0.9Se0.3,0.67\nGa1.1Sb0.9Te0.3,0.7\nGa1.2Cu0.8Se2.2,1.58\nGa1.5Cu0.5S2.5,2.43\nGa1.5Cu0.5Se2.5,1.76\nGa1.65Cu0.35S2.65,2.53\nGa1.65Cu0.35Se2.65,1.81\nGa1.6Cu0.4S2.6,2.45\nGa1.7Cu0.3S2.7,2.55\nGa1.85Cu0.15Se2.85,1.92\nGa1.8Cu0.2S2.8,2.65\nGa1.8Cu0.2Se2.8,1.86\nGa1.95Cu0.05S2.95,2.64\nGa1.95Cu0.05Se2.95,1.96\nGa1.99Cu0.01Se2.99,1.99\nGa1.9Cu0.1S2.9,2.6\nGa1As0.01P0.99,2.23\nGa1As0.2P0.8,2.2\nGa1As0.3P0.7,2.16\nGa1As0.4P0.6,2.1\nGa1As0.5P0.5,2\nGa1As0.6P0.4,1.91\nGa1As0.7P0.3,1.8\nGa1As0.8P0.2,1.62\nGa1As0.99P0.01,1.37\nGa1As0.9P0.1,1.5\nGa1Sb0.01As0.99,0.7\nGa1Sb0.14As0.86,0.66\nGa1Sb0.25As0.75,0.65\nGa1Sb0.35As0.65,0.68\nGa1Sb0.3As0.7,0.67\nGa1Sb0.85As0.15,1.1\nGa1Sb0.8As0.2,1.02\nGa1Sb0.95As0.05,1.28\nGa1Sb0.99As0.01,1.37\nGa2(TeO3)3,4.14\nGa2Cu1S3.5,2.42\nGa2CuSe4,0.63\nGa2GePbSe6,1.96\nGa2GeTe3,0.84\nGa2HgS4,2.79\nGa2HgSe4,1.95\nGa2NiS4,0\nGa2PbS4,2.38\nGa2PbSe4,1.83\nGa2S3,2.8\nGa2Se2O7,4.61\nGa2Si(AgS3)2,2.35\nGa2SiPbSe6,2.17\nGa2SnGeS6,2.04\nGa3CuTe5,1.09\nGa3Pt2,0\nGa3SiAg3Se8,2.3\nGa4Cu2Te7,1.08\nGa4PbS7,3.08\nGa4SnS7,3.1\nGa4SnSe7,2.55\nGa5Ge(PbS3)4,2.35\nGa5Ge(PbSe3)4,1.91\nGa5Pd13,0\nGa8Cu3Mo2,0\nGa9Rh2,0\nGaAgGe3Se8,2.17\nGaAgGe5Se12,2.14\nGaAgGeS4,3\nGaAgO2,2.2\nGaAgTe2,1.1\nGaAs2W,0\nGaBi,0.1\nGaBi25O39,2.99\nGaCuGeSe4,1.38\nGaCuO2,1.47\nGaFe3,0\nGaFeNi2,0\nGaGeTe,1.1\nGaHSeO4,5.51\nGaP,2.74\nGaSiAgSe4,2.63\nGaSiRu2,0\nGaTc,1.42\nGaTc2W,0\nGd(CuS)3,1.62\nGd(CuSe)3,0.14\nGd(CuTe)3,0.52\nGd(InS2)3,1.13\nGd(NiGe)2,0\nGd(SiRu)2,0\nGd1.05Sc0.95Se3,1.2\nGd1.47Mn2.04In0.49S5,1.75\nGd1.87Lu2.13Se6,1.56\nGd1Mn1.95In1.05S5,1.66\nGd2(Zn2Ge)3,0\nGd2AlCo2,0\nGd2Mn4S7,1.44\nGd2O3,5.3\nGd2S3,2.55\nGd2Se3,2.2\nGd2Te3,0.74\nGd2Zn17,0\nGd2ZrS5,1.88\nGd3(AlNi3)2,0\nGd3.04Sc0.96S6,1.5\nGd3Al0.74Si0.7S7,2.34\nGd3Al7Ag2,0\nGd3Co11B4,0\nGd3ReO7,0\nGd3S4,0\nGd4GaSbS9,2.41\nGd6Ge2.5S14,2.2\nGd6Ta4Al43,0\nGdAs,0.63\nGdB(SbO4)2,3.48\nGdB6,3.6\nGdB66,1.27\nGdCd2,0\nGdCd4B3O10,3.8\nGdGeRu,0\nGdH2NO5,4.84\nGdInIr,0\nGdN,1.54\nGdNiO3,0\nGdO2,0\nGdPbAu,0\nGdSb,0\nGdSbPd,0\nGdScS3,2.1\nGdSe2,0\nGdTe,1.3\nGdZn,0\nGdZnIn,0\nGe(Bi3O5)4,3.25\nGe(SeO3)2,5.27\nGe(WO3)6,0\nGe0.01Pb0.99Se1,0.27\nGe0.01Te0.01Pb0.99Se0.99,0.23\nGe0.01Te0.99Pb0.99S0.01,0.32\nGe0.01Te1Pb0.99,0.32\nGe0.02Te0.98Pb0.98S0.02,0.34\nGe0.03Pb0.97Se0.97S0.03,0.28\nGe0.05Pb0.95Se0.95S0.05,0.29\nGe0.05Pb0.95Se1,0.28\nGe0.05Te0.95Pb0.95S0.05,0.4\nGe0.05Te1Pb0.95,0.34\nGe0.06Te0.06Pb0.94Se0.94,0.28\nGe0.15Pb0.85Se0.85S0.15,0.34\nGe0.15Te0.15Pb0.85Se0.85,0.32\nGe0.15Te1Pb0.85,0.36\nGe0.1Pb0.9Se0.9S0.1,0.32\nGe0.1Pb0.9Se1,0.3\nGe0.1Te1Pb0.9,0.35\nGe0.25Te1Pb0.75,0.44\nGe0.2Pb0.8Se1,0.35\nGe0.2Te0.2Pb0.8Se0.8,0.36\nGe0.2Te1Pb0.8,0.4\nGe0.39Te1Pb0.61,0.56\nGe0.3Pb0.7Se1,0.4\nGe0.3Te1Pb0.7,0.48\nGe0.41Te1Pb0.59,0.49\nGe0.4Te1Pb0.6,0.51\nGe2Os,0\nGe2Sb2Te5,0.5\nGe3Bi3O10.5,3.3\nGe3Sb,0\nGe40Te5.3I8,0.8\nGe5(Te4As)2,0\nGeAs3,0\nGeI2,1.5\nGeO2,5.54\nGeP,0.95\nGePb2(SeO3)4,4.1\nGePbS3,2.4\nGePt2,0\nGeRh,0\nGeTe2,0.3\nH2Se,0\nH7Se2NO6,4.81\nHPbI3,0\nHf(CoSi)2,0\nHf(CuP)2,0\nHf(VGa2)2,0\nHf(VH2)2,0\nHf2Al3C4,0\nHf2Co4P3,0\nHf2Fe,0\nHf2Ge,0\nHf2Hg,0\nHf2MnIr,0\nHf2Ni,0\nHf2OsPd,0\nHf2ReRh,0\nHf2S,0\nHf2Si,0\nHf2Tl,0\nHf3(CuSi)4,0\nHf3(NiGe)4,0\nHf3P,0\nHf3P3Pd4,0\nHf3Sb,0\nHf3Zn3N,0\nHf4Al3,0\nHf4Co4Si7,0\nHf54Os17,0\nHf5CuPb3,0\nHf5Pb,0\nHf5Sb3,0\nHf5Sb9,0\nHf5Si4,0\nHf5Sn3,0\nHf5Sn4,0\nHf5Te4,0\nHf6PbO18,0\nHf7P4,0\nHfAlPd2,0\nHfAs2,0\nHfAsRh,0\nHfB,0\nHfB4Ir3,0\nHfC,0\nHfCo3B2,0\nHfFe2,0\nHfGaCo2,0\nHfHg4(AsCl3)2,2.47\nHfHg4(PCl3)2,3.26\nHfInCu2,0\nHfNi5,0\nHfO2,5.55\nHfOs2,0\nHfPt,0\nHfS2,2.9\nHfSe2,2.2\nHfSi,0\nHfSiPt,0\nHfTc,0\nHfTiF6,0\nHfTl3,0\nHfVSi,0\nHfZnNi2,0\nHg2Rh,0\nHg2Sb2O7,0\nHg3As,0\nHg3Bi2(SCl4)2,3.26\nHg3Bi2(TeCl4)2,2.8\nHg3C,0\nHg3PS3,1.98\nHg3PS4,2.03\nHg3Sb,0\nHg5AsS2I3,1.57\nHg7.5As4Cl6,1.73\nHg8Bi3As4Cl13,2.43\nHgBr,2.6\nHgBr2,3.59\nHgBrCl,3.4\nHgCl2,4.45\nHgI,2.37\nHgIrO3,0\nHgOsPb2,0\nHgPS3,2.6\nHgPt,0\nHgPt3,0\nHgRhO3,0\nHgS,2.1\nHgTe,0.15\nHgTeBr,2.06\nHgTeI,1.85\nHo(BC)2,0\nHo(BiO3)2,0\nHo(CuO2)2,0\nHo(CuSe)3,0.16\nHo(CuTe)3,0.26\nHo(InS2)3,1.23\nHo(MnSn)6,0\nHo(NiB)2,0\nHo(SbO3)2,0\nHo(SiOs)2,0\nHo(SiPd)2,0\nHo(SiPt)2,0\nHo(SiRu)2,0\nHo10Si17,0\nHo2Au,0\nHo2B4C,0\nHo2Co17,0\nHo2CuRh,0\nHo2Ge5Rh3,0\nHo2GeS5,2.5\nHo2HfS5,1\nHo2O3,5.42\nHo2Pd2Pb,0\nHo2S3,0.5\nHo3AlC,0\nHo3GaC,0\nHo3Ge5,0\nHo3Hg,0\nHo3Ni19B10,0\nHo3P,0\nHo3Pd2,0\nHo4C7,0\nHo4Ga16Co3,0\nHo5(Ge5Rh2)2,0\nHo5Si4,0\nHoAlAu2,0\nHoAlB14,0\nHoB2Rh3,0\nHoB4,0\nHoC2,0\nHoCd,0\nHoCd3,0\nHoCdCu4,0\nHoCo3,0\nHoCu4Pd,0\nHoGe,0\nHoGeAu,0\nHoInAu2,0\nHoInPt,0\nHoMg2,0\nHoMgAu2,0\nHoMgZn2,0\nHoMn12,0\nHoNiGe,0\nHoSb2,0\nHoSi,0\nHoSiRu2C,0\nHoTh3,0\nHoTiGe,0\nHoTiO3,0\nHoTiSi,0\nHoTlPd,0\nHoZnRh,0\nHoZnRh2,0\nICl2,0\nIn(MoSe)3,0\nIn(PSe2)2,1.29\nIn0.001Te1Pb0.999,0.3\nIn0.005Te1Pb0.995,0.43\nIn0.01Ga0.99As0.99P0.01,1.43\nIn0.01Ga0.99As1,1.4\nIn0.01Te1Pb0.99,0.53\nIn0.04Te1Pb0.96,0.37\nIn0.07Te1Pb0.93,0.32\nIn0.1Ga0.9As0.1P0.9,2.25\nIn0.1Ga0.9As0.9P0.1,1.6\nIn0.2Ga0.8As0.2P0.8,2.15\nIn0.2Ga0.8As0.8P0.2,1.58\nIn0.2Ga0.8As1,1.07\nIn0.3Ga0.7As0.3P0.7,2.05\nIn0.3Ga0.7As0.7P0.3,1.67\nIn0.3Ga0.7As1,1\nIn0.3Ga0.7P1,2.2\nIn0.4Ga0.6As0.4P0.6,1.85\nIn0.4Ga0.6As0.6P0.4,1.74\nIn0.4Ga0.6As1,0.81\nIn0.4Ga0.6P1,2.05\nIn0.4Ga1.6Cu1S3.5,2.15\nIn0.5Ga0.5As1,0.75\nIn0.5Ga0.5P1,1.9\nIn0.6Ga0.4As0.6P0.4,1.25\nIn0.72Ga0.28As1,0.55\nIn0.7Ga0.3As0.3P0.7,1.58\nIn0.8Ga0.2As0.2P0.8,1.4\nIn0.8Ga0.2As0.8P0.2,0.85\nIn0.8Ga0.2As1,0.5\nIn0.99Ga0.01As0.01P0.99,1.3\nIn0.99Ga0.01As0.99P0.01,0.3\nIn0.9Ga0.1As0.1P0.9,1.32\nIn0.9Ga0.1As0.9P0.1,0.45\nIn1.01Cu0.99Se2.01,1.08\nIn1.05Cu0.95Se2.05,1.07\nIn1.1Cu0.9Se2.1,1.06\nIn1.3Cu0.7Se2.3,1.1\nIn1.5Cu0.5Se2.5,1.24\nIn1.65Cu0.35Se2.65,1.19\nIn1.6Cu0.4Se2.6,1.32\nIn1.6Ga0.4Cu1S3.5,1.55\nIn1.7Cu0.3Se2.7,1.21\nIn1.85Cu0.15Se2.85,1.32\nIn1.8Cu0.2Se2.8,1.26\nIn1.99Cu0.01Se2.99,1.45\nIn1.9Cu0.1Se2.9,1.45\nIn11.3Bi14.7S38,1.45\nIn11Cu9Se20,0\nIn1Ag1.75Sb5.75Se11,0.94\nIn1Ga1Cu1S3.5,1.84\nIn1Hg4As2.5Br3.5,1.71\nIn1Sb0.01As0.99,0.17\nIn1Sb0.1As0.9,0.14\nIn1Sb0.2As0.8,0.12\nIn1Sb0.3As0.7,0.11\nIn1Sb0.4As0.6,0.1\nIn1Sb0.5As0.5,0.1\nIn1Sb0.6As0.4,0.13\nIn1Sb0.7As0.3,0.16\nIn1Sb0.8As0.2,0.21\nIn1Sb0.99As0.01,0.35\nIn1Sb0.9As0.1,0.27\nIn2As2Cl2O5,4.62\nIn2B(PO4)3,5.39\nIn2Bi3Se7I,1.38\nIn2Co,0\nIn2Cu1S3.5,1.43\nIn2FeSe4,1.15\nIn2GeTe3,0.68\nIn2Hg6(P2Cl3)3,3.13\nIn2HgS4,2\nIn2HgSe4,0.6\nIn2O3,2.8\nIn2Pt,0\nIn2S3,2\nIn2Se2O7,2.97\nIn2Te,0.46\nIn3AgTe5,0.68\nIn3Au10,0\nIn3Bi7(Pb2S9)2,0\nIn3CuS5,1.2\nIn3CuSe5,0.6\nIn3Pd5,0\nIn3Sb,0\nIn4As5(BrO4)3,4.22\nIn4Bi3S10,1.42\nIn4Cu2Te7,1.1\nIn4S5,0.9\nIn4Se3,0.64\nIn5AgS8,1.76\nIn5AgTe8,0.47\nIn5CuS8,1.34\nIn5Se6,0.14\nIn9AgTe14,1.5\nInAg3,0\nInAgO2,4.2\nInAgTe2,0.93\nInAsI,0.41\nInAu3,0\nInBi2S4Br,1.5\nInBi2S4Cl,1.5\nInBi2Se4Br,1.21\nInCuGeSe4,1.3\nInCuS2,1.5\nInFe2CuSe4,0\nInHg7S6Cl5,2.54\nInHgW2,0\nInPS4,3.12\nInPt,0\nInPt3C,0\nInSb2S4Br,1.8\nInSb2S4Cl,1.8\nInSb2Se4Br,1.35\nInSiIr,0\nInSiTe3,0\nInSn2As2Se,0.2\nInSnAsSe,0.26\nIr0.67S2,2\nIr0.67Se2,0.45\nIrPb,0\nIrS2,0.9\nIrSe2,0.9\nIrSeS,1.2\nK(CoSe)2,0\nK(FeAs)2,0\nK(GeSe2)2,1.8\nK(OsO3)2,0\nK0.8Sn2Hg1.2S8,2.78\nK1.25Bi7.25Pb3.5Se15,0.53\nK1.46Sn3.09Bi7.45Se15,0.39\nK1.83Cd1.83Bi2.17S6,1.37\nK10Fe4Sn4S17,2.2\nK10Mn4Sn4S17,2.3\nK10Sn3(PSe3)8,1.82\nK10Zn4Ge4S17,3.34\nK11Mn4O16,0\nK2.15Sb8.15Pb1.7Se15,0.6\nK2Ag3Sb3S7,2.2\nK2AgSnSe4,1.8\nK2Al2B2O7,6.89\nK2Au(IO3)5,2.65\nK2B10H9O,0\nK2BaNb2S11,1.77\nK2Cd(PSe3)2,2.58\nK2Cd2Te3,1.93\nK2Cd3S4,2.75\nK2Cd3Se4,2.36\nK2Cd3Te4,2.26\nK2Ce(PO4)2,2.46\nK2Dy2Ti3O10,3.38\nK2FeGe3Se8,1.95\nK2Ga3CuSe6,1.72\nK2Gd2Sb2Se9,1.33\nK2Gd2Ti3O10,3.3\nK2Ge2PbS6,2.85\nK2Ge3(BO5)2,5.38\nK2Hg(PSe3)2,2.25\nK2Hg3(GeS4)2,2.64\nK2Hg3Se1.31S2.69,2.28\nK2Hg3Se2.97S1.03,2.11\nK2Ho4Cu4S9,2.43\nK2In2P3Se10,2.2\nK2In3AgSe6,1.64\nK2In3CuSe6,1.68\nK2La2Sb2S9,2.2\nK2La2Ti3O10,3.05\nK2Mn(SnSe3)2,2\nK2Mn3S4,0\nK2MnSnSe4,1.7\nK2Mo2Se2O11,3.3\nK2NbCuS4,2.82\nK2NbCuSe4,2.14\nK2NbO6,0\nK2Nd2Ti3O10,3.25\nK2PAuS4,2.63\nK2PdSe10,1.48\nK2RbSb,1.2\nK2ReH9,5.71\nK2RuCl6,0\nK2S,2.1\nK2Sb8Se3,1.31\nK2Se,1.8\nK2Sm2Ti3O10,3.26\nK2SmP2S7,2.59\nK2Sn(AuS2)2,2.75\nK2Sn3(SbS5)2,2.3\nK2Ta15O32,0.33\nK2Te,1.9\nK2TeI6,1.38\nK2Th(CuS2)2,2.17\nK2Ti(CuS2)2,2.04\nK2VAgS4,1.85\nK2VCuS4,1.82\nK2Zn(SnSe3)2,1.71\nK2ZnTe2,3\nK3(FeS2)2,0\nK3B6ClO10,6.89\nK3Bi2I9,2.1\nK3Cd(BO2)5,3.47\nK3Cr2(PS4)3,1.35\nK3Ga3Ge7S20,3.25\nK3Ga3Ge7Se20,2.23\nK3Hg,0\nK3LiNb6O15,0\nK3NaSn3Se8,2.2\nK3Nb2AsSe11,1.53\nK3Sm(AsS4)2,2.2\nK3Sn,0\nK3Ta2AsS11,2.21\nK3Ta2AsSe11,1.45\nK3Th2Cu3S7,2.49\nK3Ti2P5S18,1.61\nK3UF3,0\nK3V,0\nK4(ZrSe5)3,1.81\nK4Ag9(SbS3)4,2\nK4Al4Si19,1.4\nK4C2O3,0\nK4Ce3Sn3S14,2.46\nK4Ga4Si19,1.18\nK4Ge(PSe3)4,2\nK4GeS4,0.8\nK4GeSe4,0.64\nK4Hf3Se14,2.02\nK5In3P6Se19,2.2\nK6Cd4Sn3Se13,2.33\nK6CdTe4,2.51\nK6Ta1.03Nb2.97S25,2.01\nK6Ta2.93Nb1.07S22,1.88\nK6Yb3(PS4)5,2.6\nK8Ce2I18O53,2.34\nK8N3O,0\nK9Bi13S24,1.4\nKAg2,0\nKAg2AsS3,2.25\nKAg2PS4,3.02\nKAg2SbS3,2.1\nKAg2SbS4,2.2\nKAgAsS2,2.21\nKAgF3,0\nKAgO,0\nKAlGeS4,3.5\nKAsSe2,1.62\nKAu(IO3)4,2.75\nKB5PbO9,3.1\nKBaAsSe3,2.26\nKBaB5O9,3.65\nKBaSbSe3,2.04\nKBi2,0\nKBi3S5,1.21\nKBiO3,0\nKBiS2,0.86\nKBiSe2,0.61\nKBr,7.6\nKC60,0\nKCd4Ga5Se12,2.16\nKCeSe4,1.54\nKCl,8.5\nKCoO2,0\nKCu2BiS3,1.29\nKCu3S2,1.46\nKCu4AsS4,1.9\nKCuPO4,0\nKCuSnS3,1.47\nKCuSnSe3,1.04\nKEuAsS4,1.89\nKEuS2,0\nKF,10.3\nKFe2BiO5,1.76\nKFeCuTe2,1.06\nKGaSe2,2.6\nKGaSnSe4,1.73\nKH(CN2)3,0\nKHg,0\nKHg11,0\nKHg2,0\nKIn(TeO3)2,4\nKInGeS4,3.1\nKInS2,3\nKInSe2,2.68\nKInSnS4,2.3\nKLi(WO3)3,0\nKLiCO3,6.32\nKLu,0\nKMo6S7,0\nKNb2O5,0\nKNb2Se,0\nKNb3(SeO6)2,3.46\nKNb3(TeO6)2,3.52\nKNbSe2O7,4\nKP(HO2)2,6.95\nKPAu5S8,2.14\nKPPbO4,4.44\nKPSe3,2.08\nKPSe6,2.16\nKRbBi8Se13,0.64\nKRuO4,0\nKSb,0.9\nKSb(SO4)2,4.64\nKSc(SeO3)2,5.4\nKScO3,0\nKSi2P3,1.72\nKSiBiS4,2.25\nKSm2CuS4,2.17\nKSnAuS3,2.3\nKSnAuSe3,2.28\nKTa3(TeO6)2,4.06\nKTa3CuO9,0\nKTaO3,3.5\nKTbSe4,1.65\nKTeP2,1.4\nKThCuS3,2.95\nKTi2F7,6.4\nKTi5Se8,0\nKTm,0\nKUClO3,2.37\nKUCuSe3,0\nKV2I3O13,2.3\nKV4Ag11O16,2\nKV6O11,0\nKY(TeO3)2,3.8\nKYb2F7,0\nKYbSe2,0\nKZn4(BO3)3,2.32\nKZrPSe6,2\nLa(FeAs3)4,0\nLa(In2Au)2,0\nLa(InS2)3,1.03\nLa(Ni2B)6,0\nLa(PRu)2,0\nLa(SiOs)2,0\nLa(SiRu)2,0\nLa1.86Tb1.14Ga1.67S7,2.67\nLa10Mn9O30,0\nLa10Se14O,2.04\nLa10Si8O3,0\nLa16Mn15O48,0\nLa1Se0.14S1.86,2.5\nLa2.1Bi5.9Pb2S14,1\nLa20Cu9O40,0\nLa20Mo12Cl4O63,2.4\nLa2B4Rh5,0\nLa2CuO4,0\nLa2Fe(SeO)2,0.7\nLa2Fe2I,0\nLa2Ga0.33Sb1S5,1.76\nLa2Ga2GeS8,2.78\nLa2Ge2Se7,1.08\nLa2Ge5Ir3,0\nLa2Ge5Rh3,0\nLa2GeSe5,1.24\nLa2HfS5,0.7\nLa2In,0\nLa2Mn(SeO)2,1.6\nLa2Nb2N2O5,0\nLa2Ni5B4,0\nLa2O3,5.4\nLa2PC,0\nLa2PI2,0\nLa2PdO4,0\nLa2Pr2O7,0\nLa2Rh7,0\nLa2S3,2.77\nLa2Si5Rh3,0\nLa2Sn5Rh3,0\nLa2TiCoO6,1.02\nLa2V2IO9,3.63\nLa2VCoO6,0.41\nLa2VNiO6,0.45\nLa2YbCuS5,1.45\nLa2YbCuSe5,1.15\nLa2Zn(SeO)2,3.4\nLa2ZrS5,2.01\nLa3(BN2)2,0\nLa3(OsO5)2,0\nLa3(ReO5)2,0\nLa3AlN,0\nLa3CuGeSe7,2\nLa3Ga1Ge0.5S7,2.54\nLa3GaCuSe7,1.36\nLa3Ge3Br2,0\nLa3In1Ge0.5S7,2.61\nLa3LuSe6,1.26\nLa3Mg0.5Sn1S14,1.71\nLa3Mo4O16F,3.7\nLa3NiBr3,0\nLa3Si1Sb0.33S7,1.92\nLa3Si1Sb0.33Se7,1.75\nLa3Te4,0.43\nLa3ZrSb5,0\nLa4Cd4In2S13,2.27\nLa4Co3O10,0\nLa4Fe(SbS5)2,1\nLa4Fe(SbSe5)2,0.85\nLa4In5S13,0\nLa4InSbS9,2.07\nLa4InSbSe9,1.76\nLa5Cu6.33S7O4,2\nLa5In3(S3O)3,2.6\nLa5SmS8,0\nLa5YbS8,0\nLa6Sb4(SO4)3,2.6\nLa8Mn7O24,0\nLa8Sb2S15,2.3\nLaAl12O19,0\nLaAl4,0\nLaAl4Co,0\nLaB6,4.1\nLaBPt3,0\nLaBeB3O7,5.65\nLaBiAu2,0\nLaCd2,0\nLaCdAg2,0\nLaCdAu,0\nLaCu6,0\nLaCuSO,3.1\nLaCuSeO,2.83\nLaCuTeO,2.31\nLaF3,6.6\nLaGa,0\nLaGa3Pd2,0\nLaGaO3,4.4\nLaGaS3,2.5\nLaGeI,0\nLaH2,0\nLaH2NO5,4.76\nLaHg,0\nLaIn,0\nLaIn2Ir,0\nLaIn5Ir,0\nLaInS2O,2.73\nLaMg(FeO3)2,0\nLaMg2H7Pd,1\nLaMg3,0\nLaNbN2O,1.7\nLaP,0.54\nLaP3,0\nLaPd3S4,0\nLaPt5,0\nLaRe2Ag,0\nLaReB,0\nLaSb,0.8\nLaScSi,0\nLaSi,0\nLaSi2,0.19\nLaSi2Ru,0\nLaSn3Ru,0\nLaTaN2O,2\nLaTb3,0\nLaV,0\nLaVI5O16,3.58\nLaYbZn2,0\nLaZnAsO,1.5\nLaZnAu2,0\nLi(CuO)3,0\nLi(NiO2)4,0\nLi0.33Ag1Sn0.67O2,2.7\nLi0.33Ti0.67Ag1O2,2.7\nLi0.5Ge1Pb1.75S4,1.95\nLi11Mn13O32,0\nLi12Fe5O16,0\nLi13Nb14ZnO42,0\nLi13Ti22O48,0\nLi14Ti21O48,0\nLi15(FeO4)4,0\nLi15Mn2O12,0\nLi17Nb20O60,0\nLi17Ti20O40,0\nLi2(FeO2)5,0\nLi2(LuGe)3,0\nLi2(NiO2)3,0\nLi23(MnAs)20,0\nLi2B4O7,7.3\nLi2CdGe,0.99\nLi2CdGeS4,3.1\nLi2CdSnS4,3.26\nLi2Co4O7F,0\nLi2CrCo3O8,0\nLi2CrCuO4,0\nLi2Cu2S3,0\nLi2CuF6,0\nLi2DyIn,0\nLi2EuSn,0\nLi2Fe2(PO4)3,0\nLi2Fe3CoO8,0\nLi2Fe3NiO8,0\nLi2Fe3SnO8,0\nLi2FeGeS4,1.42\nLi2FeSnS4,1.86\nLi2FeWO6,0\nLi2Ga,0\nLi2Ga(GeSe3)2,2.64\nLi2Ga2GeS6,3.65\nLi2GaPd,0\nLi2HgGe,0.93\nLi2HgGeS4,2.46\nLi2In2GeS6,3.45\nLi2In2GeSe6,2.3\nLi2In2SiS6,3.61\nLi2In2SiSe6,2.54\nLi2InAg,0\nLi2LaTl,0\nLi2MgHg,0\nLi2MgIn,0\nLi2MgSn,0\nLi2MnCo3O8,0\nLi2MnCu3O8,0\nLi2MnGeS4,3.06\nLi2MnNi3O8,0\nLi2MnO2F,0\nLi2Mo2Se2O11,3.3\nLi2Nb2(PO4)3,0\nLi2NdAs2,0\nLi2NdSb2,0\nLi2Ni2SbO6,0\nLi2Ni3TeO8,0\nLi2Ni5(PO4)4,0\nLi2PmAl,0\nLi2PmGe,0\nLi2PrIn,0\nLi2PrP2,0\nLi2PtO3,2.3\nLi2Si4Ni5O14,0\nLi2SiHgS4,2.68\nLi2Sn5,0\nLi2SnHgS4,2.32\nLi2SnIr,0\nLi2TeMoO6,3.5\nLi2TeWO6,4\nLi2Ti3FeO8,0\nLi2TiMn3O8,0\nLi2TlAg,0\nLi2U(MoO5)2,0\nLi2V2F7,0\nLi2V3CrO8,0\nLi2V3FeO8,0\nLi2YbPb,0\nLi2ZnGe,1.1\nLi2ZnGeSe4,1.86\nLi2ZnSnS4,2.87\nLi2ZnSnSe4,1.87\nLi3(CoO2)4,0\nLi3(CuO)4,0\nLi3(CuO2)2,0\nLi3AlP2,2.75\nLi3AlTe4O11,3.63\nLi3Bi,0.7\nLi3C,0\nLi3Co(NiO2)4,0\nLi3Co2(GeO4)3,0\nLi3Co3SbO8,0\nLi3Co4TeO8,0\nLi3Cr(NiO2)4,0\nLi3Cr3(CuO6)2,0\nLi3CrCo3O8,0\nLi3CrO4,0\nLi3Cu4NiO8,0\nLi3Dy,0\nLi3Fe(CoO2)4,0\nLi3Fe(SbO3)4,0\nLi3Fe2SbO6,0\nLi3FeNi3O8,0\nLi3FeS3,0\nLi3FeTe4O11,1.98\nLi3GaTe4O11,3.85\nLi3Mn(CuO3)2,0\nLi3Mn(NiO3)2,0\nLi3Mn2(CoO4)2,0\nLi3Mn2(PO4)3,0\nLi3Mn2CuO6,0\nLi3Mn3NiO8,0\nLi3Mn3WO8,0\nLi3Mn4(PO4)6,0\nLi3Mn4O8,0\nLi3MnAs2,0\nLi3Mo2P5O18,0\nLi3Ni(SbO3)4,0\nLi3Ni2(GeO4)3,0\nLi3Ni3(PO4)4,0\nLi3PS4,3.68\nLi3ScN2,2.9\nLi3Si3Ag2,0\nLi3Ti2(PO4)3,0\nLi3Ti3(PO4)4,0\nLi3V12O29,0\nLi3V4FeO12,0\nLi3V4NiO12,0\nLi3VOF5,0\nLi4(FeO2)9,0\nLi4.5Al0.5Te1O6,4.9\nLi4.5Cr0.5Te1O6,1.79\nLi4.5Fe0.5Te1O6,3.25\nLi4.5Ga0.5Te1O6,4.99\nLi4.5Mn0.5Te1O6,1.97\nLi4Co2Ni3O10,0\nLi4Co3CuO8,0\nLi4Co5SbO12,0\nLi4Cr3NiO8,0\nLi4CrO5,0\nLi4Cu(PO4)2,0\nLi4Fe2Cu3O10,0\nLi4Fe3NiO8,0\nLi4Fe7(OF7)2,0\nLi4FeNi3O8,0\nLi4HgGe2S7,2.75\nLi4MgNi3O8,0\nLi4Mn(WO4)3,0\nLi4Mn3Cr3O12,0\nLi4Mn5Cu3O16,0\nLi4Mn5Nb3O16,0\nLi4Mn5NbO12,0\nLi4Mn5Ni3O16,0\nLi4NbNi3O8,0\nLi4Ni2(PO4)3,0\nLi4Ni3BiO8,0\nLi4Ti5Cr3O16,0\nLi4TiCr3O8,0\nLi4V5Cu3O16,0\nLi4VF7,0\nLi4WO5,0\nLi5(BiO3)4,0\nLi5Co2Ni3O10,0\nLi5Co2O2F5,0\nLi5Cr2Ni5O12,0\nLi5Fe2Ni3O10,0\nLi5Fe6(BO3)6,0\nLi5La3Nb14O42,0\nLi5Mn2Cu5O12,0\nLi5Mn3(FeO5)2,0\nLi5Mn5(SbO6)2,0\nLi5Mn6(BO3)6,0\nLi6(NiO2)5,0\nLi6Fe3Co7O20,0\nLi6Fe9CoO20,0\nLi6FeNi9O20,0\nLi6FeO5F,0\nLi6FeO6,0\nLi6Mn5CoO12,0\nLi6Mn5FeO12,0\nLi6Tb2O7,0\nLi7(Mo3S4)4,0\nLi7(NiO2)11,0\nLi7Ca8Nb12O40,0\nLi7Ti16O32,0\nLi7Ti5O12,0\nLi7Ti7O16,0\nLi8BiS6,0\nLi8GeN4,2.61\nLi8IrO6,0\nLi8PO3,0\nLi8PrO6,0\nLi8Ti16CuS32,0\nLi8TiNi7O16,0\nLi9Fe3(WO4)7,0\nLi9Ga13(Te7O22)3,4.45\nLiAgF3,0\nLiAl2Rh,0\nLiAl2Tc,0\nLiAl3,0\nLiAlB4,0\nLiAlGe,0\nLiAlRh2,0\nLiAsS2,1.6\nLiB3,2\nLiB9PbO15,4.75\nLiBePt2,0\nLiBi2(PO4)3,0\nLiBi3(ClO2)2,3.35\nLiBiS2,0.11\nLiCa2Ga,0\nLiCa2Ge3,0\nLiCa2In,0\nLiCa2Mg,0\nLiCa3As2H,1.4\nLiCaO3,0\nLiCd2Rh,0\nLiCdBO3,4.28\nLiCl,9.33\nLiCo(CO3)2,0\nLiCo7O7F,0\nLiCoS2,0\nLiCu2(CO3)2,0\nLiCu2Ge,0\nLiCu3F7,0\nLiCu5P3O13,0\nLiCuO2,0\nLiCuPO4,0\nLiEr2Ga,0\nLiErAu2,0\nLiEuH3,1.5\nLiF,11.7\nLiFe2(PO4)3,0\nLiFe2(SiO4)2,0\nLiGa(GeSe3)2,2.64\nLiGaAg2,0\nLiGaAu2,0\nLiGaO2,5.6\nLiGaPd2,0\nLiGaPt2,0\nLiGaTe2,2.31\nLiGd5P2O13,3.73\nLiGeRh2,0\nLiH3(SeO3)2,4.9\nLiHf2Ir,0\nLiHfPd2,0\nLiHg2Pd,0\nLiHoAu2,0\nLiHoO3,0\nLiIn(IO3)4,4.27\nLiIn2Rh,0\nLiInAg2,0\nLiInS2,3.56\nLiInSe2,2.83\nLiInSn,0\nLiInSnS4,2.3\nLiInTe2,1.46\nLiLa2IrO6,0\nLiLu2Ga,0\nLiLu2Pd,0\nLiLu2Ru,0\nLiLu2Tc,0\nLiMg2Ag,0\nLiMgAs,0.7\nLiMgBi,0.4\nLiMgN,3.2\nLiMgSnPd,0\nLiMn(PO4)2,0\nLiMn2(PO4)2,0\nLiMn4O8,0\nLiMn9Se10,0\nLiMnCoO4,0\nLiMnCuO4,0\nLiMnO2,0\nLiMnP2O7,0\nLiMnSiO4,0\nLiMo3O8,0\nLiMoIO6,2.8\nLiNb3(BiO3)4,3\nLiNi2(PO4)3,0\nLiNiP2O7,0\nLiPm2Al,0\nLiPm2Ga,0\nLiPm2Ir,0\nLiPm2Si,0\nLiPr2Ru,0\nLiSb3PbS6,1.6\nLiSbS2,1.36\nLiSbSe2,0.68\nLiSbTe2,0.13\nLiScHg2,0\nLiSiB6,2.27\nLiSiPd2,0\nLiSiRh2,0\nLiSm3SiS7,2.83\nLiSn(PO3)4,0\nLiSn4Ir,0\nLiSnAu,0\nLiTa3(BiO3)4,3.5\nLiTaO3,4.1\nLiTaRh2,0\nLiThAu2,0\nLiTi11O20,0\nLiTi3O6,0\nLiTiSiO4,0\nLiTlPd2,0\nLiTm2Rh,0\nLiTm2Ru,0\nLiTmSn,0\nLiV2NiO6,0\nLiV3O4,0\nLiY(CuP)2,0\nLiY2Ru,0\nLiYbF4,0\nLiYbPb,0\nLiZn(Fe5O8)2,0\nLiZn2GaO4,4\nLiZnBO3,3.1\nLiZnN,1.91\nLiZr2Os,0\nLiZrRh2,0\nLu(InS2)3,1.27\nLu(SiOs)2,0\nLu2AgAu,0\nLu2Al3Co,0\nLu2AlTc,0\nLu2CdAg,0\nLu2CdIn,0\nLu2CrS4,1.75\nLu2Fe2Si2C,0\nLu2FeS4,0\nLu2InHg,0\nLu2MgHg,0\nLu2Mn12P7,0\nLu2Mo2C3,0\nLu2O3,5.5\nLu2TlAg,0\nLu2TlCd,0\nLu2TlCu3Se5,2.12\nLu3BC3,0\nLu3Ga,0\nLu3InN,0\nLu3TlC,0\nLu4C7,0\nLu5(Si5Ir2)2,0\nLu5Si3B,0\nLu7(NiTe)2,0\nLu7(TePd)2,0\nLuAg2,0\nLuAl2Pd5,0\nLuAlAg2,0\nLuAu,0\nLuBPd3,0\nLuC2,0\nLuCd4B3O10,3.7\nLuCdAg2,0\nLuGaRh2,0\nLuGe2,0\nLuHfRu2,0\nLuIr,0\nLuIr2,0\nLuMnSi,0\nLuNiBC,0\nLuP,1.3\nLuPt3,0\nLuScRh2,0\nLuScRu2,0\nLuScZn2,0\nLuSi2Ni,0\nLuSiIr,0\nLuU2S3O2,0\nLuUO3,0\nMg(As2Rh3)2,0\nMg(CoS2)2,0\nMg(FeO2)4,0\nMg(FeS2)2,0\nMg(SnO2)4,0\nMg(TiS2)4,0\nMg10B16Ir19,0\nMg17Al11Pd,0\nMg23Al30,0\nMg2AgIr,0\nMg2Co,0.66\nMg2CrN2,0\nMg2Cu,0\nMg2CuWO6,0\nMg2Ga,0\nMg2Ge,1.67\nMg2GeB2Rh5,0\nMg2GeSe4,2.02\nMg2MnN2,0\nMg2PdAu,0\nMg2RhAu,0\nMg2Si,2.27\nMg2SiPt,0\nMg2TcO4,0\nMg2TiIrO6,0\nMg2V9O13,0\nMg2Zr14O5,0\nMg3(B25C4)2,2.7\nMg3(MnAl9)2,0\nMg3(Ni10B3)2,0\nMg3(Ni10P3)2,0\nMg32Al36Ag13,0\nMg3Al9FeSi5,0\nMg3AsN,1.33\nMg3Bi2,0\nMg3Ga7Co2,0\nMg3Ge,0\nMg3N2,2.8\nMg3P2,1.4\nMg3Rh,0\nMg3Ru2,0\nMg3Sb2,0.8\nMg3Tl,0\nMg4Sc3(SiO3)8,0\nMg5As,0\nMg5B3O9F,5.63\nMg5Ti13O30,0\nMg5Tl2,0\nMg9CuO10,0\nMgAgAs,0\nMgCo2(PO5)2,0\nMgCr,0\nMgCu2GeS4,2.36\nMgCu2SiS4,3.2\nMgCuBi,0\nMgCuSb,0\nMgCuSn,0\nMgF2,11.1\nMgIn3,0\nMgInAg2,0\nMgInPd2,0\nMgMnO3,0\nMgMnRh2,0\nMgNiSb,0\nMgPb3,0\nMgPt5,0\nMgRh2Pb,0\nMgRhF6,0\nMgSbF6,0\nMgSbPt,0\nMgSc,0\nMgScAg2,0\nMgSi7Ir3,0\nMgSiN2,4.05\nMgSnRh2,0\nMgTe,3.6\nMgTi11O20,0\nMgTi4O6,0\nMgTl,0\nMgV4O6,0\nMgZn2,0\nMn(BW)2,0\nMn(CoO2)4,0\nMn(PbO2)2,1.5\nMn(SbO2)2,2.65\nMn(SbO3)2,0\nMn(SbSe2)2,0.31\nMn0.05Te1Pb0.95,0.37\nMn0.1Te1Pb0.9,0.49\nMn15Si26,0.7\nMn2AlB2,0\nMn2AlO4,0\nMn2CoAs,0\nMn2CoGe,0\nMn2Cu(PO4)3,0\nMn2GaW,0\nMn2GeS4,0\nMn2Hg5,0\nMn2Nb,0\nMn2OF3,0\nMn2P,0\nMn2Tl2O7,0\nMn2VSi,0\nMn3(OF3)2,0\nMn3Al10,0\nMn3Cr3(CoO8)2,0\nMn3Cr3(TeO8)2,0\nMn3NbO8,0\nMn3NiN,0\nMn3PdN,0\nMn3PtN,0\nMn3SbO8,0\nMn3V2(SiO4)3,0\nMn5As4,0\nMn5Ge2,0\nMn5O3F5,0\nMn5O7,0\nMn7O7F,0\nMnAl3,0.58\nMnAlAu2,0\nMnAs,0\nMnBe2Co,0\nMnCdO2,0\nMnCoSi,0\nMnCu2Sn,0\nMnCu3,0\nMnF2,9.9\nMnFeAs,0\nMnFeCoGe,0\nMnGaNi2,0\nMnGaPt,0\nMnGePd,0\nMnGeRh2,0\nMnIn2PbS5,1.45\nMnInCu2,0\nMnNbO4,0\nMnNi,0\nMnNiP,0\nMnO,3.6\nMnO2,1.3\nMnP2,0\nMnP4,0.28\nMnPSe3,2.5\nMnS,0\nMnSb3(PO4)6,0\nMnSbPd,0\nMnSbRh2,0\nMnSe,2.5\nMnSi,0.6\nMnSiNi2,0\nMnSnRu2,0\nMnTcOs,0\nMnTe9,2\nMnTePd,0\nMnV(TeO4)2,1.9\nMo2NCl8,0\nMo3Pd2N,0\nMo5As4,0\nMo5O14,0\nMoSe2,1.6\nNa(GeP)3,2.06\nNa0.5Ge1Pb1.75S4,2.08\nNa0.5Ge1Pb1.75Se4,1.6\nNa0.75Eu1.625Ge1Se4,2\nNa10(Ga2Sn)3,0\nNa11Bi5O16,0\nNa11Ti20O40,0\nNa15Sn4,0\nNa19Zr11S30,0\nNa2B6O9F2,7.33\nNa2Be4B4O11,7.3\nNa2Cd(GeSe3)2,2.37\nNa2CdSnS4,2.52\nNa2Cl,0\nNa2Cr7O14,0\nNa2EuGeSe4,2\nNa2Ga2GeS6,3.29\nNa2Ga2SnS6,2.2\nNa2Gd(PO4)2,4.19\nNa2Ge2Se5,2.38\nNa2Hg3(GeS4)2,2.68\nNa2Hg3Se1.49S2.51,2.03\nNa2In,0\nNa2In2GeS6,3.17\nNa2In2GeSe6,2.47\nNa2In2SiS6,3.27\nNa2In4Se6S,1.92\nNa2In5Au6,0\nNa2LiTa,0\nNa2Mo2Se2O11,3.1\nNa2Nb4Se4O19,3.56\nNa2Pt(IO3)6,2.4\nNa2S,2.4\nNa2SO4,0\nNa2Se,2\nNa2Si2Hg3S8,2.86\nNa2Sn2Hg3S8,2.45\nNa2Te,2.3\nNa2TeS3,2.35\nNa2TeSe3,1.87\nNa2Ti2Sb2O,0\nNa2Ti3O7,3.51\nNa2Tl,0\nNa2UI6,0\nNa2V6O13,0\nNa2VCuF7,0\nNa2Zn(GeSe3)2,2.36\nNa2Zn(SnS3)2,2.93\nNa2Zn3(SeO3)4,4.9\nNa3(WO3)4,0\nNa3In2Au,0\nNa3Mn2(GeO4)3,0\nNa3MoClO4,4.69\nNa3MoO4F,4.77\nNa3Re,0\nNa3Sn2ClF6,3.88\nNa3Tl,0\nNa3UF7,0\nNa3WClO4,4.99\nNa3Zn(BO2)5,3.2\nNa4Al4Si19,0.64\nNa4Eu(GeS3)2,2.15\nNa4Mg(GeSe3)2,2.53\nNa4Mg(SiSe3)2,2.85\nNa5Cu7O13,0\nNa5Fe6(SiO3)12,0\nNa5Gd(MoO4)4,3.38\nNa6CoSe4,0\nNa6FeS4,0\nNa7(CoO3)2,0.5\nNa7.36Ga7.24Sn4.78Se24,1.5\nNa8(CuO2)5,0\nNa8Hg3,0\nNa8NbO6,0\nNa8PO3,0\nNa9(WO3)16,0\nNaAlGeS4,3.6\nNaAsO3,0\nNaB15,0.32\nNaBi3,0\nNaBiS2,0.38\nNaBiSe2,0.28\nNaC,0\nNaCd2Au,0\nNaCd4P3,1.1\nNaCdAsS3,2.93\nNaCdO3,0\nNaCdSb,0\nNaCeS2,0\nNaCeS3,2.15\nNaCuO,0\nNaEuO2,0\nNaF,10.5\nNaFe2(SiO3)4,0\nNaFe2O3,0\nNaGaGe3Se8,2.35\nNaH3(SeO3)2,4.9\nNaHg,0\nNaIn(IO3)4,4.25\nNaIn(TeO3)2,4\nNaIn3S5,2.18\nNaIn3Se5,2.17\nNaInS2,1.9\nNaInSe2,2.8\nNaInSnS4,2.4\nNaInTe2,1.6\nNaIrPb,0\nNaLa2TaO6,4.5\nNaLaS3,2.61\nNaLi3,0\nNaLu(Pd3O4)2,0\nNaNb2PS10,1.72\nNaNi2O3,0\nNaSb,0.82\nNaSb(PS3)2,2.17\nNaSbF6,3.76\nNaSbTe2,0.47\nNaSc(SeO3)2,5.5\nNaSi2Pd3,0\nNaSm(PS3)2,2.54\nNaSn2,0\nNaTa3,0\nNaTi5Se8,0\nNaTl,0\nNaY(Te2O5)2,3.9\nNaYb(PS3)2,1.85\nNaZr2TiF11,0\nNaZrCuTe3,0\nNb(Cl2O)2,0\nNb17Ir3S40,0\nNb2(CoO3)3,0\nNb2AgPS10,1.78\nNb2Cr4Si5,0\nNb2O5,3.08\nNb2Pb2Se4O15,2.79\nNb2Sb,0\nNb2Tl3CuSe12,0.8\nNb2Tl4S11,1.8\nNb3(Fe10B3)2,0\nNb3B2,0\nNb3Bi,0\nNb3CuO8,1.47\nNb3In,0\nNb3IrSe8,0\nNb3Os,0\nNb3Ru,0\nNb3Te,0\nNb3V(PO4)6,0\nNb3VS6,0\nNb40N21O16,0\nNb4Co2PdSe12,0\nNb5Ga4,0\nNb5Ge3,0\nNb5OF14,0\nNb6Co7,0\nNb6VSb3O25,3.2\nNbAg2(PS4)2,2.02\nNbCrN,0\nNbCrW,0\nNbCu3Se4,2.45\nNbCuO3,2\nNbGaCo2,0\nNbHO3,0\nNbHg3F6,0\nNbOsPb,0\nNbPt2,0\nNbRu2Cl,0\nNbSe2,1.4\nNbSi2,0\nNbSiIr,0\nNbSnIr,0.28\nNd(Al4Co)2,0\nNd(AsPd)2,0\nNd(CoGe)2,0\nNd(CoSi)2,0\nNd(CrSi)2,0\nNd(GePt)2,0\nNd(InS2)3,1.15\nNd(NiSn)2,0\nNd(PRu)2,0\nNd(Re2Si)2,0\nNd(SiIr)2,0\nNd1.33Lu0.67S3,1.5\nNd10Se14O,1.98\nNd2(SnSe3)3,0.5\nNd2BC,0\nNd2CdIn,0\nNd2Fe14B,0\nNd2Ge5Rh3,0\nNd2HfS5,0.7\nNd2IrPd,0\nNd2Ni7P4,0\nNd2O3,4.4\nNd2Ru2O7,0\nNd2S3,2.65\nNd2Se3,1.7\nNd2Te3,1.12\nNd2WC2,0\nNd2ZnGa,0\nNd2ZrS5,1.83\nNd3(GeRu)2,0\nNd3AlC,0\nNd3Ge5,0\nNd3In,0\nNd3Ni13B2,0\nNd3Te4,1.6\nNd3Zr,0\nNd4(GeS4)3,2.62\nNd4Ge3Rh4,0\nNd4InSbSe9,1.57\nNd4Mg3Co2,0\nNd4MgRu,0\nNd4O3F7,0\nNd5Ge3,0\nNd5Ge4,0\nNdAgAs2,0\nNdAgPb,0\nNdAl4Ge2Au,0\nNdAl7Au3,0\nNdAs,1.04\nNdAu3,0\nNdB6,4.9\nNdBRh3,0\nNdBi,0\nNdCrGe3,0\nNdCu3(RuO3)4,0\nNdCuSO,2.98\nNdCuTeO,2.26\nNdErTl2,0\nNdErZn2,0\nNdF3,6.15\nNdFeSi2,0\nNdGa2Ni,0\nNdGaO3,0\nNdIn3,0\nNdIn5Rh,0\nNdInAu,0\nNdInCu,0\nNdLuSe3,1.61\nNdMg2,0\nNdMg2Ni9,0\nNdMgNi4,0\nNdMnSbO,0\nNdMoO4F,3.66\nNdNiC2,0\nNdO2,0\nNdPt,0\nNdRh,0\nNdSb,0\nNdSbPd,0\nNdScGe,0\nNdSmHg2,0\nNdSn2,0\nNdSnRh,0\nNdTe,0\nNdTe2,0.48\nNdTiGe,0\nNdTlAg2,0\nNdTlPd,0\nNdZn2Ag,0\nNi(CN)2,2\nNi(PO3)4,0\nNi23B6,0\nNi2Ge,0\nNi2Mo3N,0\nNi2Mo4C,0\nNi2Mo4N,0\nNi2PO5,0\nNi2Te3O8,3.84\nNi3Ge,0\nNi3Pt,0\nNi3S4,0\nNi3SnN,0\nNi4(BiO2)9,0\nNi4(PO4)3,0\nNi7(P2O7)4,0\nNiAgO2,0\nNiAsO3,0\nNiCO4,0\nNiGe,0\nNiGePt2,0\nNiI,0\nNiN,0\nNiO,4\nNiS2,0.64\nNiTe,0.23\nOsS2,2\nP2H12N7Cl,0\nP2H4RhO9,0\nP2O5,0\nP2Os,1.13\nP2Pd,0.65\nP2Pd3S8,2.12\nP2Rh,1\nP2Se3,2.4\nP2Se5,2.2\nPH2NO2,0\nPH6NO4,6.8\nPHPbO3,3.97\nPOsS,1.4\nPOsSe,1.4\nPPdS,1.38\nPPdSe,0.15\nPRuS,1.4\nPSe,2.5\nPW5O17,0\nPb17(Cl9O4)2,3.44\nPb1Se0.01S0.99,0.37\nPb1Se0.5S0.5,0.33\nPb1Se0.95S0.05,0.26\nPb1Se0.99S0.01,0.26\nPb1Se0.9S0.1,0.27\nPb2O3,1.67\nPb2SeN2O9,3.76\nPb3O4,2.12\nPb3Se2(BrO3)2,3.73\nPbN6,2.98\nPbSeO4,4.3\nPd(IO3)2,1.31\nPd16S7,0\nPd2N,0\nPd3(PbS)2,0\nPdO,0.8\nPdPb2,0\nPdS,0.5\nPdS2,0.75\nPdSe,0.2\nPdSe2,0.4\nPm2CuGe,0\nPm2IrRh,0\nPm2NiRh,0\nPm2PtAu,0\nPm3I,0\nPmCd3,0\nPmCdPd2,0\nPmDy3,0\nPmGaAu2,0\nPmHgAu2,0\nPmMgAu2,0\nPmMgCd2,0\nPmMgRh2,0\nPmSbRh2,0\nPmSnRh2,0\nPr(BRu)2,0\nPr(BiO3)2,0\nPr(CoAs)2,0\nPr(CoGe)2,0\nPr(FeSi)2,0\nPr(InS2)3,1.14\nPr(MnSi)2,0\nPr1.29Lu0.71S3,1.38\nPr10Se14O,1.89\nPr1Te1.9,1\nPr27Se40,0\nPr2Au,0\nPr2CdSn,0\nPr2Co12P7,0\nPr2Ge2Se7,1.32\nPr2GeSe5,1.8\nPr2HgPb,0\nPr2InGe2,0\nPr2InPd2,0\nPr2Ir2O7,0\nPr2S3,2.6\nPr2Se3,1.8\nPr2Te4O11,3.65\nPr3(Al2Si3)2,0\nPr3Cd,0\nPr3I,0\nPr4InSbSe9,1.89\nPr4MgRu,0\nPr4Sb3,0\nPr4Te7,0.46\nPr5In11Ni6,0\nPr5Si4,0\nPr6Fe13Si,0\nPr7Mn8O24,0\nPr9(SbO)5,0\nPrAgAs2,0\nPrAl3Ni2,0\nPrAs,1\nPrAu,0\nPrB4,0\nPrB6,4.9\nPrBN2,4\nPrBPt4,0\nPrCd,0\nPrCo4B,0\nPrCuSO,3.03\nPrErIn2,0\nPrErMg2,0\nPrFeGe2,0\nPrGaAu2,0\nPrGe3,0\nPrGe5,0\nPrGeAu,0\nPrIn,0\nPrInAu2,0\nPrIr2,0\nPrLuIn2,0\nPrLuSe3,1.56\nPrMgAg2,0\nPrMgGa,0\nPrMo3,0\nPrMoO4F,3.64\nPrNiGe2,0\nPrO,0.55\nPrP,0\nPrSb,0.66\nPrSbPt,0\nPrSm3,0\nPrSmO2,0\nPrTaN2O,2\nPrTl2InSe4,0.93\nPrTlSe2,1.18\nPrTmTl2,0\nPrZn,0\nPt0.97S2,0.95\nPt3Pb,0\nPt3PbC,0\nPtN,0\nPtS2,0.75\nPtSe2,0.1\nRb1.45Sb7.45Pb3.1Se15,0.45\nRb1.54Cd1.54Bi2.46S6,1.33\nRb15Hg16,0\nRb28(Mg3In17)3,0\nRb2AgPS4,2.6\nRb2BaNb2Se11,1.53\nRb2Cd(IBr)2,3.35\nRb2Cd(PSe3)2,2.58\nRb2Cd3(B4O7)4,4.76\nRb2Cd3S4,2.92\nRb2Cd3Se4,2.37\nRb2Cd3Te4,2.3\nRb2CrF6,0\nRb2Cu2Sb2S5,1.6\nRb2Cu2SnS4,2.08\nRb2FeI4,0\nRb2GeB4O9,5.54\nRb2Hg(PSe3)2,2.32\nRb2Hg3(GeS4)2,2.8\nRb2Mo3Se3O16,3.1\nRb2Mo9Se10,0\nRb2Na2IrO4,0\nRb2NaNiF6,0\nRb2NaVF6,0\nRb2NbCuS4,2.64\nRb2NbCuSe4,2.19\nRb2PS5,2.3\nRb2Pt(IO3)6,2.4\nRb2SCl6F,0\nRb2Sn2Hg3S8,2.48\nRb2Sn3(SbS5)2,2.33\nRb2Tb3AlF16,0\nRb2Te,4.5\nRb2TeBr6,2.14\nRb2TeI6,1.4\nRb2Ti(AgS2)2,2.33\nRb2Ti(CuS2)2,2.19\nRb2VAgS4,1.83\nRb2VCuS4,1.85\nRb2Zn3(SeO3)4,4.9\nRb3(Cu4S3)2,0\nRb3Ag9(PS4)4,2.6\nRb3Al3Ge7S20,3.1\nRb3Al3Ge7Se20,2.4\nRb3Bi2Br9,2.62\nRb3Cd(BO2)5,2.34\nRb3Ga,0\nRb3Li4(BO2)7,6.53\nRb3Mn,0\nRb3Na(MoO4)2,4.84\nRb3Nb2AsSe11,1.5\nRb3Sb,1\nRb3Sb2Br9,2.48\nRb3Sb2I9,1.94\nRb3Sm,0\nRb3Ta2AsS11,2.21\nRb3Tm,0\nRb3Zn(BO2)5,2.66\nRb4Ag9(SbS3)4,2\nRb4CuSi2O7,0\nRb4Ga4Si19,1.18\nRb4Ge(PSe3)4,2\nRb4Ge3B6O17,5.42\nRb4Mo5(PO11)2,3.51\nRb4Ti3S14,1.59\nRb5(W4O15)2,0\nRb5(WO3)18,0\nRb5B(SO4)4,3.99\nRb5Li6(BO2)11,6.53\nRb5Tl3O,0\nRb6O,0\nRb7Th2(P2Se7)3,2.07\nRb9Bi13S24,1.3\nRbAg2SbS4,2.3\nRbAg2TeS6,2.04\nRbAg5(PS4)2,2.4\nRbAgF3,0\nRbB5(H2O3)4,0\nRbBa2(PO3)5,7.6\nRbBi2,0\nRbBi3TeSe4,0.8\nRbBr3,0\nRbC8,0\nRbCaBO3,3.67\nRbCd(BO2)3,4.2\nRbCd13,0\nRbCd4Ga5S12,3.02\nRbCd4Ga5Se12,2.19\nRbCd4Ga5Te12,1.64\nRbCd4In5Se12,1.57\nRbCu(SbS2)2,1.6\nRbCu2AsS3,1.96\nRbCu2SbS3,1.67\nRbCu4AsS4,2.15\nRbCuPdF5,0\nRbCuSnS3,1.44\nRbCuSnSe3,1.04\nRbEuO2,0\nRbF,10.4\nRbF3,0\nRbGaSnSe4,1.88\nRbGe3,0\nRbGeB3O7,5.58\nRbH2(IO3)3,4.07\nRbH3(SeO3)2,4.84\nRbHg3,0\nRbHgSbTe3,0.2\nRbIn4,0\nRbIn5S6,2.5\nRbInGeS4,3.1\nRbInS2,3.3\nRbInSnS4,2.7\nRbInTe3O8,3.9\nRbLiCO3,6.28\nRbMn4Ga5Te12,1.53\nRbMn4In5Se12,1.76\nRbMnTe2,0\nRbMoPO6,2.96\nRbNa2NiO2,0\nRbNa2Sb,1\nRbNb3(TeO6)2,3.49\nRbNb4Br11,0.46\nRbNbSe2O7,4.1\nRbPPbO4,4.35\nRbPSe6,2.18\nRbPdF3,0\nRbSbO3,0\nRbSbSe2,1.62\nRbSbTe2,0.38\nRbSc(SeO3)2,4.9\nRbTa3(TeO6)2,3.88\nRbTbSe2,2.5\nRbTiBr3,0\nRbTmO3,0\nRbU2SbS8,0\nRbUAgS3,0\nRbV(CuS2)2,1.45\nRbVP2S7,0\nRbWO3,0\nRbY(TeO3)2,3.6\nRbYbZnSe3,2.07\nRbZn4In5Se12,1.76\nRbZrPSe6,2\nRe(TeCl6)2,0\nRe2PbO6,0\nRe2RuBr,0\nRe2W3C,0\nRe3As7,0\nRe3F,0\nRe3P4,0\nRe5(NiAs6)2,0\nReBiO3,0\nReCl4,0\nReF6,0\nReIr3,0\nReO3,2.3\nReOsRu,0\nRePO5,0\nReSi2,0.12\nReSn3,0\nRh0.67S2,1.5\nRh0.67Se2,0.7\nRh2S3,0.8\nRh3Pb,0\nRh7(PbO5)3,0\nRhS3,1.5\nRhSe2,0.6\nRhSe3,0.7\nRhSeS,0.7\nRu3Cl,0\nRuCl3,0\nRuS2,1.8\nRuSe2,1\nSb2I2F11,0\nSb2Os,0.2\nSb2PbSe4,1.8\nSb2Ru,0.3\nSb2Te,0\nSb2XeF14,0\nSb3IO4,2.61\nSb4Pb4S11,0\nSb5IO7,1.95\nSb6Pb4Se13,0.65\nSb6Pb6Se17,0.8\nSb8I2O11,2.72\nSbAs,1.6\nSbOsS,1.2\nSbOsSe,0.4\nSbPb2S2I3,2\nSbPbBrO2,2.67\nSbPbIO2,2.48\nSbPd3,0\nSbPt3,0\nSbRh3,0\nSbRuSe,0.9\nSbSBr,2.17\nSbSeBr,1.84\nSbTeI,1.25\nSbTeOs,0.05\nSbTeRh,0.5\nSbTeRu,0.5\nSc(CuSe)3,0.3\nSc(GaFe)6,0\nSc(TiN)9,0\nSc(VGa2)2,0\nSc11(AlGe4)2,0\nSc14Cu14O37,0\nSc2(PO4)3,0\nSc2Al3Ru,0\nSc2CuRu,0\nSc2Fe,0.77\nSc2FeB2Ir5,0\nSc2GaAg,0\nSc2GaIr,0\nSc2MnC,0\nSc2S3,2\nSc2TlTc,0\nSc3(MnGa3)2,0\nSc3(ReSi2)2,0\nSc3BPb,0\nSc3C4,0\nSc3Fe2Si3,0\nSc3GaC,0\nSc3PbC,0\nSc4Ge6Rh7,0\nSc5Bi3,0\nSc5NCl8,0\nSc5Pb3,0\nSc6FeSb2,0\nSc6NiTe2,0\nSc6Te2Os,0\nSc7CI12,0\nSc8Te3,0\nScAg,0\nScAg(PSe3)2,1.55\nScAgO2,3.8\nScAlNi2,0\nScBIr3,0\nScBPd3,0\nScBe5,0\nScCd,1.71\nScCdAg2,0\nScCdHg2,0\nScCoGe2,0\nScCoO3,0\nScCrO4,0\nScCu2,0\nScCuO2,3.3\nScGa2,0\nScGe2,0\nScHg,0.24\nScIr,0\nScN,2.6\nScNiSb,0.11\nScPPt,0\nScRh,0\nScRh3C,0\nScSbPd,0.23\nScSbRh2,0\nScSbRu2,0\nScSi3Ni,0\nScSnPd,0\nScTa2NO5,2.67\nScTiNbO6,3.58\nScTiO3,0\nScTlS2,1.51\nScTlSe2,0.79\nScTlTe2,0.85\nScZn2,0\nScZn3,0\nScZnNi2,0\nScZnPt2,0\nSeS,1.9\nSi(Bi3O5)4,3.2\nSi0.001Ge0.999,0.65\nSi0.03Ge0.97,0.67\nSi0.0645Ge0.9355,1.04\nSi0.07Ge0.93,1.04\nSi0.08Ge0.92,0.72\nSi0.109Ge0.891,1.13\nSi0.12Ge0.88,0.84\nSi0.162Ge0.838,1.32\nSi0.1Ge0.9,0.8\nSi0.226Ge0.774,1.5\nSi0.2Ge0.8,0.86\nSi0.347Ge0.653,1.91\nSi0.3Ge0.7,0.88\nSi0.458Ge0.542,2.24\nSi0.4Ge0.6,0.9\nSi0.6Ge0.4,0.94\nSi0.7Ge0.3,1\nSi0.8Ge0.2,1.1\nSi0.94Ge0.06,1.06\nSi0.98Ge0.02,1.08\nSi0.999Ge0.001,1.09\nSi0.9Ge0.1,1.04\nSi15(TeP2)4,1.24\nSi2Ni6B,0\nSi2NiP3,0\nSi2Pd9,0\nSi2Ru,0\nSi2SbO6,0\nSi3N4,5.1\nSiAs2,0.88\nSiAu3,0\nSiB3,2\nSiBi3O7,0\nSiGe,0.88\nSiHg3,0\nSiP,2\nSiP2,1.89\nSiSb,1.9\nSiSb3,0\nSiSe2,1.72\nSiSn,0.59\nSiTe2Os,0\nSiW3,0\nSm(BOs)2,0\nSm(CoSi)2,0\nSm(CuO2)2,0\nSm(CuS)3,1.82\nSm(CuTe)3,0.23\nSm(ErSe2)3,2\nSm(InS2)3,1.18\nSm(MnGe)2,0\nSm(NiSn)2,0\nSm(SiAg)2,0\nSm(SiNi)2,0\nSm1.82Lu2.18Se6,1.51\nSm2(PPt2)3,0\nSm2(SnSe3)3,0.7\nSm2AgRu,0\nSm2AlCd,0\nSm2Cu4Sn5,0\nSm2CuAs3O,0\nSm2Fe17,0\nSm2IO2,0\nSm2In,0\nSm2IrPd,0\nSm2Mn3(SbS3)4,1.5\nSm2Mo2O7,0\nSm2O3,5\nSm2Pd2Pb,0\nSm2RuAu,0\nSm2S3,2.96\nSm2Sc3,2.3\nSm2Se3,2.3\nSm2Te3,0.7\nSm2Tl,0\nSm2TlHg,0\nSm2TlZn,0\nSm2ZrSe5,1.41\nSm3(Sb7Te12)2,0\nSm3Al,0\nSm3Al0.33Si1S7,2.26\nSm3AlN,0\nSm3B(SO)3,2.5\nSm3OsO7,0\nSm3Sc,0\nSm3Te4,0.51\nSm3Zr,0\nSm4Al23Ni6,0\nSm4GaSbS9,2.23\nSm4In21Pd10,0\nSm4InSbS9,2.13\nSm4MgRh,0\nSm4U4O17,0\nSm5Br11,0\nSm6Br13,0\nSmAg,0\nSmAlCu,0\nSmAs,1.03\nSmAs2Au,0\nSmAu3,0\nSmB(SbO4)2,3.54\nSmB6,3.5\nSmB66,0.8\nSmBPd3,0\nSmBiW2O9,3.39\nSmC10,0\nSmCdHg2,0\nSmCo2,0\nSmCo3B2,0\nSmCoC2,0\nSmCrGe3,0\nSmCuO3,0\nSmCuSO,2.9\nSmCuSe2,2.1\nSmCuSeO,2.6\nSmCuSi,0\nSmErMg2,0\nSmHg3,0\nSmHgPd,0\nSmHoHg2,0\nSmHoZn2,0\nSmIn2Rh,0\nSmInAu,0\nSmLuTl2,0\nSmMg3,0\nSmMgHg2,0\nSmNi2B2C,0\nSmNiAs,0\nSmNiC2,0\nSmP,1.09\nSmPbAu,0\nSmS,2.3\nSmSb,0.59\nSmSb2,0\nSmSe,0.46\nSmSi3Pt5,0\nSmSnPd,0\nSmSnRh2,0\nSmSnTe2,0.52\nSmTh3,0\nSmTmZn2,0\nSn(PO3)3,0\nSn0.001Pb0.999Se1,0.24\nSn0.01Te1Pb0.99,0.23\nSn0.03Pb0.97Se1,0.21\nSn0.03Te1Pb0.97,0.21\nSn0.05Pb0.95Se1,0.12\nSn0.06Pb0.94Se1,0.14\nSn0.06Te1Pb0.94,0.28\nSn0.07Pb0.93Se1,0.08\nSn0.08Pb0.92Se1,0.06\nSn0.08Te0.08Pb0.92Se0.92,0.22\nSn0.08Te1Pb0.92,0.13\nSn0.13Pb0.87Se1,0.02\nSn0.15Pb0.85Se1,0.13\nSn0.15Te0.15Pb0.85Se0.85,0.18\nSn0.17Pb0.83Se1,0.04\nSn0.17Te1Pb0.83,0.15\nSn0.1Te1Pb0.9,0.16\nSn0.23Te1Pb0.77,0.04\nSn0.25Pb0.75Se1,0.04\nSn0.25Te1Pb0.75,0.04\nSn0.28Te0.28Pb0.72Se0.72,0.12\nSn0.2Pb0.8Se1,0.06\nSn0.2Te0.2Pb0.8Se0.8,0.14\nSn0.2Te1Pb0.8,0.08\nSn0.35Te0.35Pb0.65Se0.65,0.09\nSn0.99Te1Pb0.01,0.26\nSn1Se0.01S0.99,1.08\nSn1Se0.2S0.8,1.03\nSn1Se0.6S0.4,0.98\nSn1Se0.75S0.25,0.94\nSn1Se0.99S0.01,0.89\nSn2BiSI5,1.32\nSn2S,0.85\nSn2SbS2I3,1.5\nSn2WO5,2.6\nSn3As2,0.47\nSn3Ir2Se3,0.43\nSn3P3O13,0\nSn3Pd,0\nSn3WO6,2.49\nSn5(BIr3)2,0\nSn5(BRh3)2,0\nSnAs3,0\nSnB,0\nSnCl2,3.9\nSnGeS3,2.23\nSnHgO3,1.6\nSnI2,2.4\nSnI4,2.38\nSnO,3\nSnO2,3.6\nSnPt3C,0\nSnRh,0\nSnS2,2.43\nSnSb3(PO4)4,0\nSnSe2,1.62\nSnTe,0.3\nSr(CeS2)2,0\nSr(CeSe2)2,0\nSr(CoP)2,0\nSr(GaAu)2,0\nSr(In4Rh)2,0\nSr(LaS2)2,2.85\nSr(NdS2)2,2.45\nSr(PrS2)2,2.7\nSr(RuO3)2,0\nSr(Sb3Ru)4,0\nSr(YbS2)2,0\nSr0.5Ta1O3,3.7\nSr10Al4Si6O,0\nSr2Be2B2O7,8\nSr2Co2O5,0\nSr2CoReO6,0\nSr2Cu(ClO)2,0\nSr2GaCo2O7,0\nSr2GeN2,0\nSr2HoRuO6,0\nSr2La2.58Bi5.42S14,1\nSr2La2Pt1O7.13,2.52\nSr2Li2Nb3O10,0\nSr2MgIrO6,0\nSr2MgReO6,0\nSr2Pr2Pt1O7.07,3.05\nSr2ScSbO6,3.57\nSr2SmTaO6,3.38\nSr2TiO4,3.41\nSr2V2(SeO5)3,2.96\nSr2V3Se5O18,2.47\nSr2YBi2O7,0\nSr2YReO6,0\nSr2ZnReO6,0\nSr3(AlSn)2,0\nSr3(SnIr)4,0\nSr3Bi(PO4)3,4\nSr3Co2S2O5,0\nSr3Eu(PO4)3,3.99\nSr3Ge(SbSe4)2,0.75\nSr3Li4La5O12,0\nSr3Sb2,0\nSr3ScNiO6,0\nSr3Se3ClO8,4.4\nSr3Ti2O7,3.26\nSr4Ga8Ge15,0.05\nSr4Te3(ClO2)4,4\nSr4V2(Se2O7)3,2.66\nSr5Bi3,0\nSr5Cd2Sb5F,0\nSr5Sn3,0\nSr5V3O12F,4.5\nSr6Nb7O21,0\nSr7Bi23O40,0\nSr8(MnN3)3,0\nSr8.007Ge2.043Bi7.949Se24,0.74\nSr8Al7,0\nSr8Co8O23,0\nSr8Fe3N8,0\nSrAg,0\nSrAl,0\nSrB2,0\nSrB6,3.68\nSrBiClO2,3.52\nSrCd,0\nSrCdSi,0\nSrCrO4,2.45\nSrCuBi,0\nSrGe2,0.9\nSrIn2,0\nSrIn2(GeIr)4,0.25\nSrIn2Ir,0\nSrIn2Rh,0\nSrIn4Ir,0\nSrIn4Pt,0\nSrLa3MnO8,0\nSrLaMn2O6,0\nSrLi2Sn,0\nSrLi4(BO3)2,6.67\nSrMgIn3,0\nSrMgSnSe4,2\nSrMnGe,0\nSrN2,0\nSrNi2(PO4)2,0\nSrNi5As3,0\nSrO,5.7\nSrPb3,0\nSrPb3Br8,3.2\nSrPbO3,1.78\nSrRhF6,0\nSrS,4.76\nSrSbAu,0\nSrSe,4.42\nSrSeO4,4.75\nSrSiPd,0\nSrSnO3,4.1\nSrSnP,0\nSrTaNO2,1.99\nSrTe,3.73\nSrTh(PS4)2,3.02\nSrTl2,0\nSrTlHg2,0\nSrUS2,0\nSrV13O18,0\nSrZnSO,3.1\nSrZnSb2,0\nSrZr2Nb,0\nTa11(CuO15)2,2.59\nTa11(CuO6)5,2.58\nTa22(CuS12)3,0\nTa2Mn3O8,1.89\nTa2MoOs,0\nTa2N,0\nTa2Nb3O12,0\nTa2O5,4.2\nTa2OsW,0\nTa2PtSe7,0\nTa2TiN3,0\nTa2Tl4S11,1.26\nTa2TlO6,0\nTa3B4,0\nTa3P,0\nTa4AlC3,0\nTa4FeTe4,0\nTa4N5,0\nTa5N6,0\nTa6Be15Cu8,0\nTa6Ni16Ge7,0\nTa7Cu3O19,2.47\nTaAl3,0\nTaAlPt,0\nTaAs,0\nTaBe2,0\nTaCoSn2,0\nTaCu3S4,3\nTaF3,0\nTaGaPt,0\nTaInNi,0\nTaN,2.3\nTaNiB2,0\nTaPd3,0\nTaPt3,0\nTaRh3,0\nTaTiFe2,0\nTaTlS3,0.78\nTaW3,0\nTb(Al2Fe)4,0\nTb(AlC)3,0\nTb(CoB)2,0\nTb(CoGe)2,0\nTb(CuSe)3,0.16\nTb(CuTe)3,0.46\nTb(FeP3)4,0\nTb(GePd)2,0\nTb(GeRh)2,0\nTb(InS2)3,1.2\nTb(MnGe)6,0\nTb(Ni2P)2,0\nTb0.52Pr2.48Ga1.67S7,2.61\nTb10B7C10,0\nTb11S16,0\nTb2AlCo2,0\nTb2C3,0\nTb2EuSe4,2\nTb2GeS5,2.1\nTb2In16Pt7,0\nTb2O3,3\nTb2Sb5,0\nTb2SbO2,0\nTb2Ti3Ge4,0\nTb3(MnC3)2,0\nTb3FeB7,0\nTb3Ge5,0\nTb3Ni13B2,0\nTb3ReO7,0\nTb3Si,0\nTb4Al2O9,4.59\nTb4GaSbS9,2.44\nTb5Ti5O17,0\nTb5Tl3,0\nTb6PbSe10,0\nTbB(SbO4)2,3.53\nTbBRh3,0\nTbBe13,0\nTbCl,0\nTbCo2,0\nTbCu5,0\nTbGa,0\nTbGa2Co3,0\nTbGa3,0\nTbH2,0\nTbHg2,0\nTbIn2Ni,0\nTbInAg2,0\nTbInIr,0\nTbMn5Ge3,0\nTbNi5,0\nTbNiGe2,0\nTbNiO3,0\nTbP,0\nTbPt,0\nTbRh2,0\nTbSb2,0\nTbSe2,0\nTbSnAu,0\nTbTe,0\nTbTl,0\nTbWClO4,4.24\nTbYHg2,0\nTbYbHg2,0\nTbYbRh2,0\nTbZn2,0\nTbZrSb,0\nTc3Pd,0\nTcB,0\nTcS2,1\nTcSe2,0.88\nTe0.01Pb1Se0.99,0.26\nTe0.05Pb1Se0.95,0.26\nTe0.4Se0.6,1.2\nTe0.5Pb1Se0.5,0.29\nTe0.5Se0.5,1\nTe0.6Se0.4,0.7\nTe0.8Se0.2,0.4\nTe0.99Pb1Se0.01,0.3\nTe2Au,0\nTe2Mo(WS2)3,0\nTe2Mo2WSe4,0\nTe2Mo3Se4,0\nTe2MoWS2,0\nTe2Os,0.3\nTe2Pd,1.8\nTe2Pd3,0\nTe2Pd3Pb2,0\nTe2Ru,0.25\nTe2W2SeS,0\nTe3MoWS,0\nTe4Mo(WS)2,0\nTe4MoW3S4,0\nTeAs,0.74\nTeI,1.1\nTeI4,1.1\nTeMoSe,0\nTeO2,3\nTePb3Cl4O3,3.79\nTePd,0\nTeSe,1.58\nTeWCl9,0\nTh(Al2Fe)4,0\nTh(Al5Fe)2,0\nTh(FeGe)2,0\nTh(FeSi)2,0\nTh(GePd)2,0\nTh(MnGe)2,0\nTh(SiRu)2,0\nTh2CrN3,0\nTh2Fe7,0\nTh2GeSe2,1.98\nTh2In,0\nTh2Se5,0.37\nTh3B2C3,0\nTh6Mg23,0\nThAl,0\nThAl3,0\nThAsSe,0\nThBi2,0\nThCrB4,0\nThFe2SiC,0\nThHg2,0\nThIr5,0\nThMn4(CuO4)3,0\nThPSe,0\nThPd3,0\nThRh2,0\nThRu3C,0\nThS,0\nThSO,2.22\nThSeO,1.65\nThSi,0\nThSi2Ru3,0\nThTeO,1.45\nThU8O18,0\nTi(Bi3O5)4,3.09\nTi10O11,0\nTi11O18,0\nTi13S24,0\nTi1C0.9,0.3\nTi20(Sb3Se)3,0\nTi2AlV,0\nTi2B,0\nTi2BRh6,0\nTi2Be17,0\nTi2C,0\nTi2Cd,0\nTi2CoGe,0\nTi2CoS4,0\nTi2CuS4,0\nTi2MnFe,0\nTi2NiH,0\nTi2NiSe4,0\nTi2OsRu,0\nTi2RePd,0\nTi2ReRh,0\nTi2ReRu,0\nTi2Sb(PO4)3,0\nTi2TcNi,0\nTi2TcPd,0\nTi2ZnS4,0\nTi3Be,0\nTi3Cu3O,0\nTi3Fe3O,0\nTi3PO7,0\nTi3Pt5,0\nTi3SnC2,0\nTi4NiBi2,0\nTi4O5,0\nTi4ZnO8,0\nTi5(B6O13)2,0\nTi5Zn4(TeO6)3,0\nTi5ZnO7,0\nTi6H2O13,3.4\nTi9O10,0\nTi9O8,0\nTiAl,0\nTiAlAu2,0\nTiAsRh,0\nTiAuCl,0\nTiBi25O39,3.1\nTiBr2,0\nTiC,0\nTiCoGe,0\nTiCoSb,0.95\nTiCoSn,0\nTiCr3(PO4)6,0\nTiFe2,0\nTiFe2As,0\nTiFe2Sb,0\nTiFe2Si,0.4\nTiFeH2,0\nTiGaIr2,0\nTiHgO3,0\nTiI,0\nTiMn2Al,0\nTiMn2Ge,0\nTiNiSb,0.42\nTiO2,3.3\nTiOs3,0\nTiPO4,0\nTiPd,0\nTiReN3,0\nTiS2,1.95\nTiS3,0.9\nTiSe,0\nTiSe2,1.55\nTiTc2Sb,0\nTiTe2,1\nTiTlPS5,1.3\nTiTlS2,1\nTiTlSe2,0.56\nTiV4CuO12,0\nTiZn3,0\nTl(Cu3S2)2,0\nTl(MoSe)3,0\nTl(WO3)3,0\nTl0.001Te1Pb0.999,0.3\nTl0.005Te1Pb0.995,0.48\nTl0.01Te1Pb0.99,0.59\nTl0.04Te1Pb0.96,0.57\nTl0.07Te1Pb0.93,0.54\nTl16O15F17,0\nTl2.35Sb8.65Se14,0.6\nTl2BiP2S7,1.8\nTl2CdTe4,0\nTl2Cu2SnS4,1.4\nTl2GeTe3,0.36\nTl2Hg3S4,2.05\nTl2Hg3Se4,1.57\nTl2Hg3Te4,0.9\nTl2InGaSe4,2.05\nTl2InGaTe4,0.88\nTl2Mo7O22,0\nTl2O3,2.25\nTl2PAuS4,2.2\nTl2S,1\nTl2Se,0.37\nTl2Te3As2Se,0.67\nTl2TeBr6,2.06\nTl2TeI6,1.47\nTl2TeS3,1.6\nTl3AsSe3,1.3\nTl3Cr,0\nTl3Ir,0\nTl3Pb,0\nTl3Si,0\nTl4CdI6,2.8\nTl4CuTeO6,2.2\nTl4In3GaS8,2.63\nTl5Te3,0\nTl6Cu(TeO5)2,2.3\nTl8Os8O27,0\nTl9SbSe6,0\nTlAgSe2,0.72\nTlAgTe2,0.1\nTlAsS2,2.15\nTlAsSe2,1.35\nTlBiTe2,0.12\nTlBiTe3,0.5\nTlCdS2,1.5\nTlCoBi,0\nTlCoMo2,0\nTlCr5(Se3S)2,0.75\nTlCr5(SeS)4,0.85\nTlCr5(SeS3)2,0.94\nTlCr5S8,1.01\nTlCr5Se3S5,0.89\nTlCr5Se5S3,0.8\nTlCr5Se7S,0.71\nTlCr5Se8,0.67\nTlCr5SeS7,0.97\nTlCuCl3,2.98\nTlCuSe2,1.07\nTlFeI3,0\nTlGaS2,3.4\nTlGaSe2,1.65\nTlGaTe2,1.8\nTlHg6S4Br5,3.03\nTlHg6Se4Br5,2.8\nTlInGeS4,2.3\nTlInHgS3,1.74\nTlInTe2,0.62\nTlN,1.4\nTlN3,3.58\nTlNi,0\nTlPS2,1.6\nTlPSe2,0.5\nTlS,1.36\nTlS2,1.8\nTlSbSe2,0.82\nTlSbTe3,0.38\nTlSn,0\nTlSnAuSe3,1.2\nTlTe,0\nTlTeP,0.3\nTlZn2Tc,0\nTm(CoSi)2,0\nTm(CuGe)2,0\nTm(CuS)2,0\nTm(CuTe)3,0.14\nTm(FeSi)2,0\nTm(GeRu)2,0\nTm(MnGe)6,0\nTm(NiGe)2,0\nTm(SiOs)2,0\nTm2AlOs,0\nTm2CdHg,0\nTm2CuTc,0\nTm2Ga10Os3,0\nTm2In,0\nTm2IrPd,0\nTm2MgRu,0\nTm2MgTl,0\nTm2O3,4.53\nTm2Ru2O7,0\nTm2ZnAg,0\nTm2ZnGa,0\nTm2ZnHg,0\nTm2ZnOs,0\nTm3(GePd)4,0\nTm3GaC,0\nTm4In(NiGe2)2,0\nTm4Sb2Se11.68,1.22\nTm5(Ge5Rh2)2,0\nTm5Ti5O17,0\nTmAl4Ni,0\nTmAlCu,0\nTmAs,1.18\nTmAu,0\nTmAu2,0\nTmB2C,0\nTmBPd3,0\nTmBRh3,0\nTmCdAg2,0\nTmCoSi2,0\nTmCu4Ag,0\nTmCuSi,0\nTmGe,0\nTmH2,0\nTmIn3,0\nTmLuPd2,0\nTmMg2Sc,0\nTmMgAg2,0\nTmMgCd2,0\nTmMnGe,0\nTmMnO3,0\nTmPd,0\nTmSb,0\nTmScHg2,0\nTmSnRh,0\nTmSnRu2,0\nTmThRu2,0\nTmTl,0\nTmU2S3O2,0\nU(Al2Fe)4,0\nU(BH4)4,0\nU(CoGe)2,0\nU(CrC)4,0\nU(CuP)2,0\nU(MnSi)2,0\nU(SiNi)2,0\nU11O5,0\nU2(Co7B2)3,0\nU2Al3C4,0\nU2AlCo2,0\nU2AlCo3,0\nU2Cl5O2,0\nU2Cr30P19,0\nU2Cu2As3O,0\nU2MnN3,0\nU2Re2C3,0\nU2SnRh2,0\nU2TeN2,0\nU2Ti,0\nU2Zn17,0\nU3Bi4,0\nU3Cu2Se7,0\nU3Nb,0\nU3Ni3Sn4,0\nU3Se4,0\nU4N7,0\nU4Re7Si6,0\nU4S3,0\nU5Ge3,0\nU6Co,0\nUAl3,0\nUAl4,0\nUAlNi4,0\nUAu2,0\nUCo4Sn,0\nUCoSi,0\nUCuP2,0\nUFe5Si3,0\nUFeSi,0\nUGa2,0\nUGa3Ni,0\nUGa5Ir,0\nUGaNi,0\nUGeRh,0\nUHg3(TeCl3)2,2.6\nUHg4(AsCl3)2,1.9\nUNiSn,0\nUO,1.5\nUO2,2.18\nUP2S7,1.41\nUP2S9,1.41\nUPt3,0\nUSbSe,0\nUSeS,0\nUSi3,0\nUVC2,0\nV12P7,0\nV2(OF)3,0\nV2Bi4O11,2\nV2Cd2Te2O11,2.48\nV2GaSn2,0\nV2NO,0\nV2OsRu,0\nV2Pb4(Se2O7)3,3.37\nV2Sb(PO4)3,0\nV2Si2O7,0\nV2TcRu,0\nV2Zn3TeO10,2.96\nV2ZnO4,0\nV3(HO2)4,0\nV3Ag,0\nV3As2O9,0.76\nV3Bi(PbO4)3,2.5\nV3Cd4(TeO5)3,2.66\nV3CrO10,0\nV3Cu,0\nV3CuO8,0\nV3Pb2Se5O18,3.14\nV3Pt,0\nV3Re,0\nV3Si,0\nV3SiNi2,0\nV4ZnO8,0\nV5SiB2,0\nV6AgO15,0\nV6PbO11,0\nV8O,0\nVAg(IO4)2,2.24\nVAg(PSe3)2,0\nVAg2I3O11,2.16\nVB2,0\nVBi(SeO4)2,2.2\nVBi24O41,3.25\nVCo,0\nVCu3(PO4)4,0\nVCu3S4,1\nVFeRu2,0\nVFeSb,0.46\nVGa(TeO4)2,3\nVIn(NiO3)2,1.92\nVIr,0\nVIr3,0\nVNi2,0\nVNi5(PO4)6,0\nVO,0.3\nVP,0\nVP4,0\nVPO4,0\nVPt2,0\nVSb,0\nVTc,0\nVTe2,0\nVTeHO5,2.51\nVZn2BiO6,2.4\nVZnRu2,0\nW2C,0\nW2N,0\nW3O7F,0\nWCl3,0\nY(Al2Cu)4,0\nY(Al5Fe)2,0\nY(AlSi)2,0\nY(CrSi)2,0\nY(CuSe)3,0.88\nY(CuSi)2,0\nY(CuTe)3,0.72\nY(FeSi)2,0\nY(NiP)2,0\nY(Re2Si)2,0\nY(SiPt)2,0\nY(SiRh)2,0\nY(SiRu)2,0\nY(TiGa2)2,0\nY2AlZn,0\nY2C3,0\nY2CuO4,0\nY2Fe2Si2C,0\nY2Ge2O7,0\nY2Ge5Ir3,0\nY2Mo2O7,0\nY2O3,5.6\nY2ReB6,0\nY2Ru2O7,0\nY2S3,2.9\nY2U3O11,0\nY3(Fe31B7)2,0\nY3Al3NiGe2,0\nY3Fe29,0\nY3GaCo3,0\nY3GaS6,2.88\nY3Ge4,0\nY3Si3Pd2,0\nY3Tm,0\nY4AsSe3,0\nY4C7,0\nY4CuTe8,0\nY4GaSbS9,2.06\nY4US5O3,1.95\nY6Zn(SiS7)2,2.38\nYAgO3,0\nYAlGe,0\nYAlPd,0\nYAs,0\nYB2C,0\nYB2Rh2C,0\nYB66,0.8\nYBi,0\nYCd4B3O10,3.78\nYCdHg2,0\nYCdPd2,0\nYCdPt2,0\nYCo2,0\nYCoO3,0\nYCu3(WO3)4,0\nYCuO2,3.5\nYErRh2,0\nYH2,0\nYH2NO5,4.83\nYHg2,0\nYIn2Ni,0\nYMg4Cu,0\nYMgAl,0\nYMgCu4,0\nYMgGa,0\nYMoClO4,3.82\nYMoO4F,3.78\nYN,1.9\nYNi4B,0\nYSbPd,0.27\nYSbPt,0.16\nYScO2,0\nYSi2,0\nYSiNi,0\nYSiRu,0\nYSn3,0\nYTi4(CuO4)3,0\nYTiO3,0\nYTmCu2,0\nYV(BiO4)2,2.09\nYVSeO10,2.7\nYVTeO10,2.2\nYWO3,0\nYZn5,0\nYZnBiO4,1.58\nYb(Al2Mo)2,0\nYb(AlGa)2,0\nYb(AlGe)2,0\nYb(AlSi)2,0\nYb(CuS)3,1.56\nYb(CuSe)3,0.2\nYb(Fe2Ge)2,0\nYb(Ga4Co)2,0\nYb(GaS2)2,2.3\nYb(GaSe2)2,1.8\nYb(HO)3,0\nYb(IO3)3,0\nYb(InS2)3,1.31\nYb(MnAs)2,0\nYb(SbS2)2,1.12\nYb(SbTe2)2,0.34\nYb(SiAg)2,0\nYb(SiRh)2,0\nYb11(Ni10C)6,0\nYb14Ti10O41,0\nYb16S29,0\nYb2(ZnGe)3,0\nYb23Mg4Cu7,0\nYb2Ce8O19,0\nYb2EuS4,1.6\nYb2EuSe4,1.3\nYb2Ge2Ir,0\nYb2HgPb,0\nYb2InPd2,0\nYb2MgS4,0\nYb2MgSe4,0\nYb2O3,5.22\nYb2SmS4,0\nYb2Sn,0\nYb2ZnPb,0\nYb3Al5O12,0\nYb3Sn13Rh4,0\nYb3Tc,0\nYb3Ti3O14,0\nYb3V,0\nYb4Sb2S11.25,1.71\nYb4Sb3,0\nYb5Au4,0\nYb6U3O17,0\nYb8Ge3Sb5,0\nYbAg2,0\nYbAgGe,0\nYbAgO2,0\nYbAl3,0\nYbAs,1.02\nYbB2Rh3,0\nYbB66,1.27\nYbBO3,0\nYbCdHg2,0\nYbCe2CuS5,1.37\nYbCe2CuSe5,1.05\nYbCuGe,0\nYbCuSi,0\nYbDyPd2,0\nYbGa2Pd,0\nYbGeRh,0\nYbH2ClO2,0\nYbIn4Ni,0\nYbIn4Rh,0\nYbIr2,0\nYbMgPd,0\nYbMn2O5,0\nYbNd2CuS5,1.35\nYbNd3,0\nYbNdAg2,0\nYbPO4,0\nYbPmPt2,0\nYbPr11Se16,0\nYbPr2CuS5,1.25\nYbRh2,0\nYbSb,1\nYbSb4Te7,0.22\nYbSe,1.5\nYbSi2Ni,0\nYbSm2CuS5,1.28\nYbSmRh2,0\nYbSn2Pd,0\nYbSnRh,0\nYbSnTe2,0.75\nYbTe,1.8\nYbTlS2,0\nYbTlSe2,0\nYbWClO4,4.23\nYbZnAu2,0\nYbZnPt,0\nZn(Bi19O29)2,2.88\nZn(CoO2)2,0\nZn(CuO2)2,0\nZn(FeN)2,0\nZn(GaSe2)2,1.72\nZn0.01Ga0.99As0.99Se0.01,1.39\nZn0.01Ga0.99P0.99S0.01,2.25\nZn0.01Ga0.99P0.99Se0.01,2.24\nZn0.01Ga0.99Sb0.99Te0.01,0.72\nZn0.05Ga0.95Sb0.95Te0.05,0.85\nZn0.15Ga0.85As0.85Se0.15,1.47\nZn0.1Ga0.9Sb0.9Te0.1,1\nZn0.25Ga0.75As0.75Se0.25,1.51\nZn0.25Ga0.75P0.75Se0.25,2.18\nZn0.2Ga0.8Sb0.8Te0.2,1.15\nZn0.2Hg0.8Te1,0.07\nZn0.3Ga0.7P0.7S0.3,2.3\nZn0.42Ga0.58As0.58Se0.42,1.67\nZn0.4Hg0.6Se1,0.42\nZn0.55Hg0.45Se1,0.8\nZn0.5Ga0.5As0.5Se0.5,1.52\nZn0.5Ga0.5P0.5Se0.5,2.13\nZn0.65Hg0.35Se1,1\nZn0.6Ga0.4As0.4Se0.6,1.8\nZn0.75Cd0.25Se1,3.2\nZn0.75Hg0.25Se1,1.4\nZn0.7Ga0.3As0.3Se0.7,1.93\nZn0.7Ga0.3P0.3Se0.7,2.15\nZn0.85Ga0.15As0.15Se0.85,2.25\nZn0.85Hg0.15Se1,1.8\nZn0.86Hg0.14Te1,1.66\nZn0.8Hg0.2Se1,1.4\nZn0.8Hg0.2Te1,1.4\nZn0.92Hg0.08Te1,1.9\nZn0.94Hg0.06Te1,2.03\nZn0.95Ga0.05P0.05Se0.95,2.4\nZn0.99Ga0.01As0.01Se0.99,2.59\nZn0.99Ga0.01P0.01S0.99,3.7\nZn0.99Ga0.01P0.01Se0.99,2.6\nZn0.99Ga0.01Sb0.01Te0.99,2.1\nZn0.99Hg0.01Se1,2.6\nZn0.9Ga0.1As0.1Se0.9,2.34\nZn0.9Ga0.1P0.1S0.9,2.8\nZn0.9Ga0.1P0.1Se0.9,2.3\nZn0.9Hg0.1Se1,1.75\nZn0.9Hg0.1Te1,1.74\nZn2BIr2,0\nZn2InCuSe4,1.1\nZn2InCuTe4,1.05\nZn2MoSeO7,4.2\nZn2Ni9O13,0\nZn2Sb3O8,0\nZn2SnN2,0\nZn2TeMoO7,4.1\nZn2WN2,0\nZn3(BO3)2,2.6\nZn3(PS4)2,3.07\nZn3.5Ga1Sn0.5O6,2.99\nZn3Cd,0\nZn3Cu,0\nZn3Cu10(TeO6)6,0\nZn3N2,0\nZn3P2,1.15\nZn4.5Ga1Sn0.5O7,3\nZn5.5Ga1Sn0.5O8,2.99\nZn6S5Cl2,2.71\nZn8Ag5,0\nZnAgF5,0\nZnAs,0.9\nZnB12(H5O12)2,4.6\nZnCrO2,0\nZnCu2GeS4,2.1\nZnCu2GeSe4,1.63\nZnCu2SiSe4,2.33\nZnCu2SiTe4,1.47\nZnCu2SnSe4,1.44\nZnCu2SnTe4,1.39\nZnCu3P3O13,0\nZnGaRh2,0\nZnHg3(SCl2)2,2.65\nZnHg3(SeCl2)2,2.23\nZnI2,4.53\nZnIrO3,0\nZnSb,1.05\nZnSb2MoO7,3.3\nZnSb3,0\nZnSi(AgS2)2,3.28\nZnSiAs2,2.12\nZnSiP2,2.07\nZnSn3,0\nZnSnO3,3.9\nZnTc,2.37\nZnWO2,0\nZr(Fe2Si)2,0\nZr(Ni2P)2,0\nZr0.67Ta1.33N3.03O0.12,1.71\nZr1.33Ta0.67N1.63O1.89,2.48\nZr1.33Ta0.67N1.97O1.38,2.31\nZr1.33Ta0.67N2.61O0.42,1.93\nZr1.86Cu1S4,1.26\nZr2(Co7B2)3,0\nZr2Al,0\nZr2Co12P7,0\nZr2CuS4,0\nZr2HBr2,0\nZr2In5Ni,0\nZr2Ni12P7,0\nZr2Se,0\nZr2Te,0\nZr3(Al2C3)2,0\nZr3(Cu2Si3)2,0\nZr3Ag,0\nZr3Al2,0\nZr3Hg,0\nZr3Ir,0\nZr3NiO,0\nZr3O,0.2\nZr4AlNi2,0\nZr4Co4Ge7,0\nZr5Al3,0\nZr5Al3C,0\nZr5Sb3,0\nZr5SiSb3,0\nZr5Sn3,0\nZr5Sn4,0\nZr6Al2CoH10,0\nZr6Al2Ni,0\nZr6NiCl15,0\nZr6O,0.18\nZr6Sb2Pt,0\nZr7P4,0\nZr7Sb4,0\nZrAl5Ni2,0\nZrAlPt,0\nZrAlRu2,0\nZrAlW,0\nZrAu4,0\nZrB2,0\nZrC,0.6\nZrCd,0\nZrCrSi2,0\nZrGaPt,0\nZrGe2,0\nZrGeRu,0\nZrHCl,0\nZrHg4(AsCl3)2,2.48\nZrHg4(PCl3)2,3.22\nZrInCu2,0\nZrInPd2,0\nZrInRh2,0\nZrIr2,0\nZrMo3,0\nZrNiGe,0\nZrNiSb,0.55\nZrNiSn,0\nZrO2,4.99\nZrPd2,0\nZrPd3,0\nZrRe2,0\nZrRh,0\nZrRu3C,0\nZrS2,2.75\nZrSb,0\nZrSbRu,0\nZrSe,0\nZrSe2,2\nZrSi2,0\nZrSiTe,0\nZrTaN3,1.72\nZrTe,0\nZrTi2O,0\nZrTiF6,0\nZrW2,0\n"
  },
  {
    "path": "dataset/matbench_expt_gap/matbench_expt_gap.json",
    "content": "[\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ag(AuS)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ag(W3Br7)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ag0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ag0.5Ge1Pb1.75Se4\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ag2BBr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ag2BiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ag2GeS3\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ag2GeSe3\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ag2HgI4\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ag2Mo(I2O7)2\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ag2P2PbO7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ag2PdO2\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ag3AsO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ag3Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ag3RuO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ag5IO6\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ag7(SI)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ag7AsS6\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ag7AsSe6\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ag7NO11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ag8GeS6\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ag8SnSe6\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ag9(PbO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ag9Ge2IO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AgAsSe2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgAu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgBi(PS3)2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AgBi(PSe3)2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgBiPbS3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgBiPbSe3\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AgBiS2\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AgBiSe2\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AgBr\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgCNO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"AgCl\\n\",\n        \"output\": \" 5.13\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AgF\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AgGeO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AgO\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AgP15\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AgPd(IO3)3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgPdO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgPt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AgSO4\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AgTe2As\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Al(Ni10B7)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Al(NiS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al0.01Cd0.99Sb0.01Te0.99\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Al0.01Ga0.99P1\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Al0.01In0.99P1\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.05Cd0.95Sb0.05Te0.95\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al0.15Ga0.85As1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.1Cd0.9Sb0.1Te0.9\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.1In0.9P1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al0.2Ga0.8P1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al0.2In0.8P1\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al0.35Ga0.65As1\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Al0.3Ga0.7As1\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Al0.3In0.7P1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.45Cd0.55Sb0.45Te0.55\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.4Cd0.6Sb0.4Te0.6\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al0.4Ga0.6P1\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al0.4In0.6P1\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al0.5Ga0.5As1\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Al0.6Ga0.4As1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al0.6Ga0.4P1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Al0.6In0.4P1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.75Ga0.25As1\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.7In0.3P1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.8Ga0.2P1\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al0.99Cd0.01Sb0.99Te0.01\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al0.99Ga0.01P1\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al0.99In0.01P1\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al10V\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al13Ru4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Al2(CuSe2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Al21Pt8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al2CoIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al2Cr2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al2CrS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al2Cu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al2FeNi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al2Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Al2S3\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al2Se3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al3Tc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Al4Cu2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al4Cu9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Al5Rh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al6Fe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Al6Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al6Tc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al7(CN)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Al9Co2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al9Ir2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Al9Rh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AlAgO2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AlAgS2\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AlAgSe2\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"AlAgTe2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AlAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AlB2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AlBi\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"AlCoO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AlCu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AlCu7O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AlCuS2\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AlCuTe2\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"AlFe2Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AlFe4(CuO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"AlIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AlNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AlPd5I2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AlSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AlV(TeO4)2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"AlVCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"As2Ir\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"As2O3\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"As2Os\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"As2Rh\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"As2Ru\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"As2S5\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AsAu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AsBr3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AsOsS\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AsP\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AsPPd\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AsPPt\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AsPRu\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AsPd3Pb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"AsRuS\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AsS\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"AsS3\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AsSI\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"AsSeBr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AsSeI\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Au3S\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"AuBrO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"B2Mo(PbO2)6\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"B2O3\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"B2Se2O7\\n\",\n        \"output\": \" 4.64\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"B3H2Pb2O7.5\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"B3Pb10Br3O13\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"B3Pb3NO10\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"B4C\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"B4H2Pb6O13\\n\",\n        \"output\": \" 3.24\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"B4W\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"B5Mo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"B6As\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"B6P\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BAs\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BH(PbO2)2\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BMo\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BP\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BPb2ClO3\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BPb6BrO7\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BPb7Br3O7\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BSb\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BSbPbS4\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BSe2Cl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BTe2As\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba(AsPd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba(AsRh)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba(BRh)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba(FeS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba(GaS2)2\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba(GaSe2)2\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba(InS2)2\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba(InSe2)2\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba(NiP2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba(PdO2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba(SnO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba(ZnAs)2\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba1.88Ta15O32\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba12In4S19\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba14Ir8(PdO11)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba14Na8CaN6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba23Ga8(SbS19)2\\n\",\n        \"output\": \" 2.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2B4H2O9\\n\",\n        \"output\": \" 5.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2B6H4O13\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2B6O11\\n\",\n        \"output\": \" 5.17\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2BiSbO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2CaOsO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2CaReO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2Cd(BO2)6\\n\",\n        \"output\": \" 4.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2Ce2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2CeInTe5\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2CoWO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2Cu5F14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2CuWO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2DyCu3O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2DyGaSe5\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2DyGaTe5\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2DyInSe5\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2DyInTe5\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2ErGaSe5\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2ErGaTe5\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2ErInSe5\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2ErInTe5\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2FeMoO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2FeReO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2Ga8GeS16\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2Ga8SiS16\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2GaAsSe5\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2GaBiS5\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2GaBiSe5\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2GaBiTe5\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2GaS4\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2GaSbSe5\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2GaSbTe5\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2GaSe4\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2GdGaSe5\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2GdGaTe5\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2GdInSe5\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2GdInTe5\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2HgS5\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2In2S5\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2In2Se5\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2InAgS4\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2InBiS5\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2InSbSe5\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2LaIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2LiFe2N3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2NaCu3S5\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2NdGaS5\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2NdGaSe5\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2NdInSe5\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2NdInTe5\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2ReNiO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2Sb7HO14\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2ScIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2ScTaO6\\n\",\n        \"output\": \" 4.19\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2SmCu3O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2SmGaSe5\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2SmGaTe5\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2SmInSe5\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2SmInTe5\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2SmTaO6\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2SnSe4\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2SnSe5\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2TaInO6\\n\",\n        \"output\": \" 4.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2TbIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2ThCu2Se5\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2UCuO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2V2Te2O11\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2V2ZnO8\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2V4(TeO6)3\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba2YGaSe5\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2YGaTe5\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2YInSe5\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2YInTe5\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba2YReO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba2Yb(CuO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2Zn0.2B2S5.2\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba2ZnSe3\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba2ZnTe3\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3(AlGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3(LiSn2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba3Ag2(SnS4)2\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3B1.5Sb0.5S6\\n\",\n        \"output\": \" 3.01\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3BSbS6\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3BSbSe6\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3Bi0.5B1.5S6\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3Bi2TeO9\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3CaIr2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3CaRu2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba3Cd(SnS4)2\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3Co10O17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3CrS5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3Dy2(PS4)4\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3Er2(PS4)4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3ErRu2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba3Eu(PO4)3\\n\",\n        \"output\": \" 4.09\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3FeS4Br\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3Gd2(PS4)4\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3GeS5\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3Ho2(PS4)4\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3In2(PO4)4\\n\",\n        \"output\": \" 3.87\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba3InS4Cl\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba3La3(Cu3O7)2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba3MgTa2O9\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3N2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3NaIr2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3NaIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3Nb2CoO9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3Nb2Se9\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3P3ClO10\\n\",\n        \"output\": \" 6.89\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3PN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3Sb2S7\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3Sn(SbSe4)2\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3Sn0.87Bi2.13Se8\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3Ta2Se9\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3Ta2ZnO9\\n\",\n        \"output\": \" 4.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba3Ta5NO14\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3Tb2(PS4)4\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3Te\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba3ThSe7\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3V2(SeO4)4\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba3YIr2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba3Yb4O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba3ZrRu2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba4B11O20F\\n\",\n        \"output\": \" 7.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba4Ga4GeSe12\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba4Ga4SnSe12\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba4Ga5AgS12\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba4Ga5CuS12\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba4Ga5CuSe12\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba4Ga5Si18\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba4Ge3S9Cl2\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba4Ge3Se9Cl2\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba4InAgSe6\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba4InCuSe6\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba4LiGa5Se12\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba4Nb14O23\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba4Sb3S8Cl\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba4Si20Au3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba4Si3Se9Cl2\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba4Sm2Cu2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba4Yb(CuO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba5(Ga2Se5)2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba5(GaSe4)2\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba5Al2Ge7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba5Bi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba5Cd(Ga2Se5)3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba5Ga6GeP12\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba5Ga6SnP12\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba5Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba5In4Bi5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba5In4Te4S7\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba5Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba5V3O12F\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba6Al4B14O33\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba6Ga2SnSe11\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba6In2NF\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba6Sn6Se13\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ba7(SnS3)5\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ba7B3O9F5\\n\",\n        \"output\": \" 4.94\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ba7Ga5AgS15\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba7Ru4Br2O15\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba8Al10B12O41\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba8Hg4Se7S5\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ba8Sn4S15\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ba8Ta7O24\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaAgSbS3\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaAl2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaAl4Se7\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaAlCu4O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaAu(IO3)5\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaB6\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaBClF4\\n\",\n        \"output\": \" 6.89\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaBSbS4\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaBiClO2\\n\",\n        \"output\": \" 3.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaCaB2O5\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaCaSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaCdSnS4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaCu2SnSe4\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaCuSbS3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaCuSbSe3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaCuTeF\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaDy2CuO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaEu2Mn2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaGa2GeS6\\n\",\n        \"output\": \" 3.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaGa2SiS6\\n\",\n        \"output\": \" 3.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaGa2SiSe6\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaGa4S7\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaGa4Se7\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaGe2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaGe3Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaGe4(IrS3)2\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaGe4(IrSe3)2\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaGe4(RhSe3)2\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaHgS2\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaHgSe2\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaIn2(P2O7)2\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaIn2Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaLa2CoS5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaLa2In2S7\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaLa2In2Se7\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaLa2Te5O14\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaLi4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaMn4O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaMn4ZnO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaMnO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaNa2GeS4\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaNa2GeSe4\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaNa2SnS4\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaNa2SnSe4\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaNaB5O9\\n\",\n        \"output\": \" 4.78\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaNb4O6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaO\\n\",\n        \"output\": \" 4.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaPd(IO3)4\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaPdSe6\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaPrO3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaPt5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaReH9\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaS\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaSi2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaSn2S5\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaSnO3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaTaNO2\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaTbMn2O6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaTe\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaTeMo2O9\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaTh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaTi14O28\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaTi4O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaTi4O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaTl(MoO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaTl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaUSe3\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaV2SeO8\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BaYb2O4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaYbSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaZn(MoO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BaZn5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BaZnGeSe4\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BaZnSO\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BaZnSiSe4\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Be12Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Be22Re\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Be2HgTe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Be2W\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Be3N2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Be3Sb2\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BeAlB\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BeCu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BeFe2Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BeGaO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BeGaRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BeO\\n\",\n        \"output\": \" 10.39\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BePd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BePd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BeS\\n\",\n        \"output\": \" 4.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BeSe\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BeSiOs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BeSiRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BeTcSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BeTe\\n\",\n        \"output\": \" 2.89\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi0.002Te0.003Pb0.999Se0.999\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi0.04Te0.06Pb0.98Se0.98\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi0.2Sb1.8Te3\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi0.2Te0.3Pb0.9Se0.9\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi0.4Sb1.6Te3\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi0.4Te0.6Pb0.8Se0.8\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi0.6Sb1.4Te3\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi1.4Sb0.6Te3\\n\",\n        \"output\": \" 0.17\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi1.6Sb0.4Te3\\n\",\n        \"output\": \" 0.16\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi1.8Sb0.2Te3\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi1.98Sb0.02Te3\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Bi12PO20\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Bi12Rh12O41\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi1Sb0.15\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi2(BO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi2(MoO4)3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi24BO39\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi2AsClO4\\n\",\n        \"output\": \" 3.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi2CO5\\n\",\n        \"output\": \" 3.42\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi2I4O13\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi2Mo2Se2O13\\n\",\n        \"output\": \" 3.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi2Pd3S2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi2Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi2SI2O11\\n\",\n        \"output\": \" 3.74\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi2Se3\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2SeI2O11\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi2Te0.03Se2.97\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi2Te0.1Se2.9\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2Te0.3Se2.7\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2Te0.45Se2.55\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi2Te0.4Se2.6\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Bi2Te0.6Se2.4\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2Te0.9Se2.1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi2Te1.2Se1.8\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi2Te1.5Se1.5\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi2Te2.1Se0.9\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi2Te2.4Se0.6\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2Te2.7Se0.3\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2Te2.97Se0.03\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi2Te2SO10\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2Te2Se\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Bi2Te3\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Bi3BTeO9\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi3I4O13F3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Bi3Se2NO11\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi4I\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi4Pb7Se13\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi4Pd(SeO3)4\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Bi5IO7\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Bi7O5F11\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Bi8Te7S5\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Bi9S6O7.5\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BiAs2Os\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BiBPbO4\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BiBr3\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BiBrO\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BiClO\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BiIO3F2\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BiO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BiP3(PbO4)3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BiPO4\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BiPb2S2I3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"BiPbClO2\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BiPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BiSBr\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"BiSCl\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BiSI\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BiSbTe3\\n\",\n        \"output\": \" 0.19\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BiSe\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BiSeI\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"BiSeO3F\\n\",\n        \"output\": \" 3.83\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"BiTeI\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"BiTeNO6\\n\",\n        \"output\": \" 3.62\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CBr4\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CI4\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca(AgGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca(Al4Co)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca(AlZn)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca(BC)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca(BIr)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ca(BiO2)2\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca(CoGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca(CoS2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca(GdS2)2\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca(GeRh)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca(LaS2)2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca(MnAs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca(NdS2)2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca(Ni2O3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca(PrS2)2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca(SiPd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca(SmS2)2\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca(TiS2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca10Ge16(B2O17)3\\n\",\n        \"output\": \" 5.47\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca11Bi10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca11Ga7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ca2Bi2O5\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca2CdAs2\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca2CdPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca2Co9O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca2CuWO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca2Ge\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca2GeN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca2Mn9O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca2MnAlO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca2NiIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca2Os2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ca2PbAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca2ScSbO6\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca2Si\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca2SmTaO6\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca2Sn\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca2Sn2F3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ca2SnS4\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca2Ti9O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca2TlCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ca2ZnRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca3(GaPt)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca3Al2Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca3Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca3Au4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca3Bi(PO4)3\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca3BiAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca3BiSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca3Cu2(ClO2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca3In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca3La2(SnS4)3\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca3N2\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca3PbN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca3Sb2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca3SbN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca3Sn2S7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca3Ti2(SiO4)3\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca3TlN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca3Zr17O37\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca4Al3O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca4Bi6O13\\n\",\n        \"output\": \" 2.76\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca5(Bi7O13)2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca5Au2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ca5B3O9F\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca5Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca5Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ca5Sn4S13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ca6Ag16N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ca6Cu2Sn7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaAgF5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaAu5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaB6\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaCdPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaCdSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaCu5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaEu2O3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaEuO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaF2\\n\",\n        \"output\": \" 9.92\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CaGa3Ni2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaGaAu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaGaGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaHfZn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaI2\\n\",\n        \"output\": \" 5.98\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaIn2Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CaIn4Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaInAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaInPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CaIrO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaMg2N2\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CaMgSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaMnSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CaNi5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaOsO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaPd3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaPrZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaSnO3\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CaTaNO2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaTi4O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaTiO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CaVO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CaYbInSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CaZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaZn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CaZn3Ni2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CaZn5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CaZnSO\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd(GaS2)2\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd(In15Te23)2\\n\",\n        \"output\": \" 1.17\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd(PS2)2\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.01Ga0.99Sb0.99Te0.01\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd0.01Hg0.99Se1\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.01In0.99Te0.01As0.99\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.02In0.98Te0.02As0.98\\n\",\n        \"output\": \" 0.73\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.03In0.97Te0.03As0.97\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd0.04In0.96Te0.04As0.96\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.05Ga0.95Sb0.95Te0.05\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.05In0.95Te0.05As0.95\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.06In0.94Te0.06As0.94\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.07In0.93Te0.07As0.93\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.1Ga0.9Sb0.9Te0.1\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd0.1In0.9Te0.1As0.9\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd0.204Hg0.796Te1\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.23Hg0.77Te1\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd0.28Hg0.72Te1\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd0.2Ga0.8Sb0.8Te0.2\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd0.2In2.4Ag0.4Te4\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd0.35Hg0.65Te1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd0.37Hg0.63Te1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.3Hg0.7Se1\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd0.3Hg0.7Te1\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.4Hg0.6Se1\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd0.5Hg0.5Se1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd0.5In2.25Ag0.25Te4\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd0.5In2.2Ag0.4Te4\\n\",\n        \"output\": \" 0.19\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.6Hg0.4Se1\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.75In2.1Ag0.2Te4\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd0.7Hg0.3Se1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.8Hg0.2Se1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd0.8In2.1Ag0.1Te4\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.99Ga0.01Sb0.01Te0.99\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd0.99Hg0.01Se1\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd0.9Hg0.1Se1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd12Ge17(B4O29)2\\n\",\n        \"output\": \" 4.29\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd13I28\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd1Se0.01S0.99\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd1Se0.2S0.8\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd1Se0.35S0.65\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd1Se0.45S0.55\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd1Se0.65S0.35\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd1Se0.99S0.01\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd2AgRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd2InAgTe3\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd2InCuTe3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cd2InCuTe4\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd2PbO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd3AgPS6\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd3Bi(PO4)3\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd3Bi2\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd3In2(Te2S)2\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd3P2\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd3Sb2\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd3Te2MoO10\\n\",\n        \"output\": \" 3.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd4P2Br3\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cd4P2Cl3\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd4P2I3\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd4Sb2I3\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd4Sb3\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cd5Ga2(Te3S)2\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cd6P7\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cd8B5O15F\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdAg2(PS3)2\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdAg2GeS4\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdAsPd5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CdAuO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdBiClO2\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdBr2\\n\",\n        \"output\": \" 4.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdCl2\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdCu(SeO3)2\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdCu2GeS4\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CdCu2GeSe4\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CdCu2SnS4\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdCu2SnSe4\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CdF2\\n\",\n        \"output\": \" 6.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CdHIO4\\n\",\n        \"output\": \" 4.35\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdHg4(AsI2)2\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdHg6(As2Br3)2\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CdI2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CdIClO3\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CdIn\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CdIn8Te13\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CdInCuSe3\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdO\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdP4PbO12\\n\",\n        \"output\": \" 4.85\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CdPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CdPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CdRhF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CdSb2Se3Br2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdSb4MoO10\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CdSnO3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce(AlZn)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce(BC)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce(CoAs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce(CoB)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce(CuSb)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce(HO)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce(InS2)3\\n\",\n        \"output\": \" 1.11\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce(MnGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce(MnSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ce(PPt2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce(SiAu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce(SiNi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce(SiPd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce1.3Lu0.7S3\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce10Se14O\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce15B8N25\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce1Mn0.5Se1O1\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ce2(SbPd3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce2(SnSe3)3\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce2Al2Co15\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce2Co5B2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce2CrN3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce2Cu(NO)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce2Fe(SeO)2\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce2Fe17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce2Ge2Se7\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce2GeSe5\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce2S2O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce2S3\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce2Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce2Se3\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce2SiSeO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce2Ti2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce2ZnNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce3(Al3Ru)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce3Al\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce3AlC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce3B2(ClO2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ce3In3Ru2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce3LuSe6\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce3MnAlS7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce3MoO7\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce3NbS3O4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce3Pd5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce3SiPt5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ce3Ta(ClO2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce3TaO7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ce4(GeS4)3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce4Bi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce4FeSe6O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce4InSbSe9\\n\",\n        \"output\": \" 1.69\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce4Si3Rh4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce4Te7\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce5(SiN3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ce5CuSe8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce5Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce5Si3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce6B2(CBr)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ce8Sb2S15\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ce8U2O21\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ce9SmO20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeAgSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CeAl2Pd5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeAl2Pt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CeAl3Ni2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CeAlO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeAlSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeAsPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeAsSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeB2Ir3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeBC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CeBiW2O9\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CeCd2Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeCdAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeCoGeH\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CeF3\\n\",\n        \"output\": \" 4.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CeGaO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeHSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeInIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeIr5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeLu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeMg2Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeMgAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeMgNi4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeMgPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CeMgZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeMoO4F\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeN\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeNbO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CeO2\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeOs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CePd5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CePrO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeSI\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeSbO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeScO3\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeSi2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeSi2Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeSiI\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeSiIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CeSiOs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeTaN2O\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeTl2P2S7\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CeTl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CeTlZn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CeZnPO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Co(PO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Co(WO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Co1Te1.88\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Co2B4Mo\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Co2Ge\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Co2O3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Co2Te3O8\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Co3H\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Co3Se4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Co3W\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Co5Ge7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Co5RuO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Co7Mo6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Co7Re17O48\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CoAs3\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CoAsRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CoAsS\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CoAsSe\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CoCu2Sn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CoGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CoH2(SN)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CoMoP2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CoN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CoOF\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CoP2\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CoP3\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CoPS\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CoSb2\\n\",\n        \"output\": \" 0.17\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CoSb3\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cr(FeSe2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr(MoS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cr10Sb3Te7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cr2CuS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr2CuTe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr2GeC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cr2HO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cr2HgSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cr2NiS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr2O3\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr2P3O11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr2SbTe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr3N2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr3Ni(PO4)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cr3P\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cr3Se4\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cr4As3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cr4Cu3Te8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cr7C3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CrAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CrB2(PbO2)6\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CrBi2I2O11\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CrCo2Bi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CrCoGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CrCoPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CrCu2Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CrFe2Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CrFeP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CrH9(CN2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CrIrO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CrIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CrNi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CrNiAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CrNiP2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CrO2\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CrO3\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CrPbO4\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CrSb2\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CrSi2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CrTe2\\n\",\n        \"output\": \" 0.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs(AsRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs(MoO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs0.4K0.6P1Se6\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs1.13Cd1.13Bi2.87Se6\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs1.43Cd1.43Bi2.57S6\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs10Cd4Sn4S17\\n\",\n        \"output\": \" 3.16\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2AgBiBr6\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2AgBiCl6\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2Al2B2O7\\n\",\n        \"output\": \" 4.13\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2Ba3(P2O7)2\\n\",\n        \"output\": \" 6.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2Cd(PSe3)2\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2Cd0.25Hg5.75S7\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2Cd1.35Hg4.65S7\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2Cd2Bi2S5\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2Cd3(B4O7)4\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2Cd3Te4\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2CrCl4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2Cu(PS3)3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2Cu2Sb2S5\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2DyCu3Te4\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2Ga2S5\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2Ga2Se5\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2Hg(ICl)2\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2Hg3I8\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2Hg3S4\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2Hg6S7\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2La1.19Bi8.81S16\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2Li3(BO2)5\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2MgGe3Se8\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2MgSn3Se8\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2Mo15S19\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2NaCoF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2NaMgF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2NaMnF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2NbCuSe4\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2P2PdSe6\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2PdSe8\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2Pt(IO3)6\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2SCl6F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2Sb\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2SeClF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2SiB4O9\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2Sn(PSe3)2\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2Sn3(SbS5)2\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2Te\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2TeBr6\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2TeI6\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2Th(PS3)3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs2Ti(AgS2)2\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2VAgS4\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2Zn3(SeO3)4\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs2ZnGe3S8\\n\",\n        \"output\": \" 3.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs2ZnGe3Se8\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs2ZnGe3Te8\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs2ZnSn3Se8\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs39Ga53(Se16Cl)6\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs3As\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs3Bi2Br9\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs3Bi2I9\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs3Li4(BO2)7\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs3NaZn2Ge21\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs3Nb2AsSe11\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs3Nb9(TeO8)4\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs3PW3O13\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs3Sb\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs3Sb2Br9\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs3Sb2I9\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs3Sn3Cl7F2\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs3V2Cl9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs4Ag9(SbS3)4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs4BiAs3Se7\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cs4Ga4Si19\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs4Ge(PSe3)4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs4Ge5(PbS4)4\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cs4In8GeSe16\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cs4Zr3S14\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cs5Bi(PSe3)4\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs5Mo21Se23\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs5P5Se12\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cs6.4Na1.6Ga8Ge38\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsAg2AsS3\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsAg2TeS6\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsAg5Te3\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsAgCl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsAgSb4S7\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsAu\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsB3O5\\n\",\n        \"output\": \" 7.42\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsBi2\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsBi3Se5\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsBiS2\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsBiSe2\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsCaO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsCd4Ga5S12\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsCd4Ga5Se12\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsCd4Ga5Te12\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsCd4In5Se12\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsCd4In5Te12\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsCdBO3\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsCdInSe3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsCeCdSe3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsCeHgSe3\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsCu(SbS2)2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsCu2AsS3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsCu2SbS3\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsDy9(Cd2Se9)2\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsEr9(Cd2Se9)2\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsErZnSe3\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsEuF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsF\\n\",\n        \"output\": \" 10.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsGa(SnSe3)2\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsGa7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsGaS3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsGaSnSe4\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsGdO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsGdZnTe3\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsGe5BO12\\n\",\n        \"output\": \" 4.89\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsGeB3O7\\n\",\n        \"output\": \" 5.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsGeI3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsH3(SeO3)2\\n\",\n        \"output\": \" 4.77\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsHo9(Cd2Se9)2\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsIn(SnSe3)2\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsInGeSe4\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsInHgS3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsInI3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsInS2\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsInSe2\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsInSnS4\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsInTe2\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsInTe3O8\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsIrO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsK(PSe4)2\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsLaHgSe3\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsLi(B3O5)2\\n\",\n        \"output\": \" 6.89\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsLiCO3\\n\",\n        \"output\": \" 6.19\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsLu7S11\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsLu7Se11\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsMg149\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsMn4Ga5Te12\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsMn4In5Se12\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsMn4In5Te12\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsMnSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsNa2Sb\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsNa8(B7O12)3\\n\",\n        \"output\": \" 4.67\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsNb6I11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsNbSe2O7\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsNi2F6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsPPbO4\\n\",\n        \"output\": \" 4.39\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsPSe4\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsPSe6\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsRb(PSe4)2\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsRb2Sb\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsRbP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsSb(SO4)2\\n\",\n        \"output\": \" 4.68\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsSbS2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsSbSe2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsSbTe2\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsSc(SeO3)2\\n\",\n        \"output\": \" 5.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsScBr3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsSmCdSe3\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsSmHgSe3\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsTa3(SeO6)2\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsTaPSe6\\n\",\n        \"output\": \" 2.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsTb9(Cd2Se9)2\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsTbZnTe3\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsTiCl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsTiF4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsTm9(Cd2Se9)2\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsUCuS3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsVP2S7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CsWCl6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsYCdSe3\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsYHgSe3\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsYTe3O8\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsYbCoSe3\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CsYbMnSe3\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsZn2B3O7\\n\",\n        \"output\": \" 5.69\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CsZn4In5Se12\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CsZn4In5Te12\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CsZrPSe6\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cu(IrS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu(NO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cu0.96Bi2Se3I1\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu1.8S1\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cu10Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu11Sb4S13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cu15Si4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu18S11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cu23(Sb4S13)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cu25Se26\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu2GeS3\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu2H3ClO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cu2Hg2SF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cu2HgGeSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu2O\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu2OF2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu2PHO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cu2Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cu2Te3O8\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cu2WSe4\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cu3(BiI4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cu3(P2O7)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cu3Bi6S10I\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu3Hg2(Te3O8)2\\n\",\n        \"output\": \" 2.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu3Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu3SbSe4\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu3Se2(ClO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Cu4As2O9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu4H10SO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu4Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu4Sn7S16\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu4W(SCl)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Cu5(Si2O7)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu6PbO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu7Hg6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Cu8O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cu9O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Cu9S5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Cu9Se4(Cl3O7)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CuBS2\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CuBi(PSe3)2\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuBiPbS3\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CuBiPbSe3\\n\",\n        \"output\": \" 0.07\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CuBiSO\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuBiSeO\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CuCN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuClO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuF\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuHg(SeO3)2\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CuMoO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CuN3\\n\",\n        \"output\": \" 4.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuNi(CN)4\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuP2(HO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"CuPO4F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuPS3\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CuPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuPtO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"CuSbPbS3\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"CuSbS2\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"CuSbSe2\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"CuSeO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Dy(Al2Cu)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Dy(CoGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Dy(CuSe)3\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy(CuSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy(CuTe)3\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Dy(GeRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Dy(InS2)3\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy12C6I17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy12Co7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Dy1Te1.4\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Dy1Te1.45\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Dy1Te1.7\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Dy2(GePt3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2(MoO4)3\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Dy2AlCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Dy2CdPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Dy2CuOs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy2MgIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy2MgTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2Ni12P7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Dy2O3\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy2S3\\n\",\n        \"output\": \" 2.91\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2Sn5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2Te3\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2Ti3Si4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2TlCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy2ZnIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy3(CuGe)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy3Al0.5Si1S7\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy3Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy3GaS6\\n\",\n        \"output\": \" 2.81\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy3InC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy3MnB7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy4CdRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Dy4GaSbS9\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy4Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy4Te3S4\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy5Pb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Dy5Sn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Dy6FeTe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Dy7In(CoGe3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"DyAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"DyAgGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"DyAgHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"DyAs\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"DyB2Rh2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"DyB6\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"DyBPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"DyBiPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"DyBiPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"DyCd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"DyCoSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"DyFeSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"DyGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"DyInAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"DyInCu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"DyInPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"DyIr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"DyMn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"DyNiGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"DyNiSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"DyPO4\\n\",\n        \"output\": \" 6.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"DyRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"DyS2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"DySiIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"DySn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"DySnRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"DyYAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"DyZnGa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"DyZnRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"DyZrRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"DyZrSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Er(Al10Cr)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Er(CrSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Er(CuGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Er(CuTe)3\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Er(InS2)3\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Er(ReO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Er(SiPd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Er2(Ga3Co)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Er2(MoO4)3\\n\",\n        \"output\": \" 0.96\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Er2C3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Er2Fe14B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Er2Mg3Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Er2MnC4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Er2O3\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Er2Se3\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Er2SnAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Er2Te3\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Er3Al3NiGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Er3SnC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Er3Te4\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Er4NiB13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Er5Bi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Er5NiPb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Er5Si3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Er6MnBi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ErAgSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ErAl9(Fe2Si3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErAlGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ErB2Ir3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErB2Ru3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErB6\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErBPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErBiW2O9\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ErCu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErCuPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ErFeC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ErHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ErLu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ErMg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ErNi4Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ErNi4B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErNiSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ErPbAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ErRu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ErSe2\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ErSiPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ErSnAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ErTe\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ErTlPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ErZn12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Eu(AlAu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu(AsPd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Eu(BiSe2)2\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu(BiTe2)2\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(CdSb)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu(ClO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu(DySe2)2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Eu(ErSe2)2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(FeSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu(GaS2)2\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu(GaSe2)2\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu(GaTe2)2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu(HoSe2)2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu(InAs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu(InS2)2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu(InSe2)2\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu(InTe2)2\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(LuSe2)2\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(MgBi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu(MnGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu(Ni2B)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(NiAs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(POs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(SbS2)2\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu(SbSe2)2\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(TmSe2)2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(ZnGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu(ZnSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu1.75Ag0.5Ge1S4\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu1.83Ta15O32\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu2(Ga3Rh)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu2C(NO)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Eu2CuO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu2Ga2GeS7\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu2Ge(BO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu2O3\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu2PBr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu2ReO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu2Se3\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Eu2SnSe5\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu2TeO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu3(InP2)2\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Eu3As2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu3BWO9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu3Bi4S9\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu3P2\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu3S4\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu3Sb4S9\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Eu3Sb4Se9\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu3Se4\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Eu3Sn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Eu4Te7\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Eu7(Ga3Sb4)2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuAgSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuAl2O4\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuAlO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"EuB(SbO4)2\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuBi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuBiW2O9\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuCd11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuClO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuCo8P5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"EuCu2SnS4\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuCu9Sn4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"EuCuSeF\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuCuSeO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"EuGe3Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"EuH2\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"EuIn2(GeIr)4\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuN\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"EuNiGe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuO\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuPPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuRhO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuS\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"EuSb4S7\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuSb4Te7\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuSbO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuScO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuSe\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"EuSeClO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"EuSnAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"EuSnO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuSnTe2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"EuTiClO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"EuTiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"EuTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"EuZn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Fe(PdSe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Fe10O9F11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Fe12As5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Fe2B(PO4)3\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Fe2Cu(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Fe2O2F3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Fe2O3\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Fe2S\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Fe3B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Fe3N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Fe3Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Fe4H15(IO8)3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Fe4O7F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Fe4Si2Sn7O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Fe6O7F5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Fe6W6C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Fe9Co7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"FeAg3(CN)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"FeAgSe2\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"FeAs2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"FeAsSe\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"FeBi(SeO3)3\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"FeBi25O39\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"FeCo2Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"FeCoAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"FeCuSe2\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"FeCuTe2\\n\",\n        \"output\": \" 0.16\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"FeI2\\n\",\n        \"output\": \" 5.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"FeOF\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"FeP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"FeP4\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"FePS\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"FePd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"FeRhO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"FeSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1As0.1P0.9\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga0.001Te1Pb0.999\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga0.005Te1Pb0.995\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga0.01Te1Pb0.99\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga0.04Te1Pb0.96\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga0.07Te1Pb0.93\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga0.95Hg0.05Sb0.95Te0.05\\n\",\n        \"output\": \" 0.69\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga0.99Hg0.01Sb0.99Te0.01\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga0.9Hg0.1Sb0.9Te0.1\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.001Sb0.999Se0.003\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1.001Sb0.999Te0.003\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1.002Sb0.998Se0.006\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1.002Sb0.998Te0.006\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1.005Sb0.995Se0.015\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1.005Sb0.995Te0.015\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.01Cu0.99Se2.01\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1.01Sb0.99Se0.03\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1.01Sb0.99Te0.03\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1.02Sb0.98Se0.06\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.02Sb0.98Te0.06\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1.05Sb0.95Se0.15\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1.05Sb0.95Te0.15\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1.1Cu0.9Se2.1\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1.1Sb0.9Se0.3\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1.1Sb0.9Te0.3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1.2Cu0.8Se2.2\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1.5Cu0.5S2.5\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1.5Cu0.5Se2.5\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1.65Cu0.35S2.65\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1.65Cu0.35Se2.65\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.6Cu0.4S2.6\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.7Cu0.3S2.7\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.85Cu0.15Se2.85\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1.8Cu0.2S2.8\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.8Cu0.2Se2.8\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.95Cu0.05S2.95\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1.95Cu0.05Se2.95\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1.99Cu0.01Se2.99\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1.9Cu0.1S2.9\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1As0.01P0.99\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1As0.2P0.8\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1As0.3P0.7\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1As0.4P0.6\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1As0.5P0.5\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1As0.6P0.4\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1As0.7P0.3\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1As0.8P0.2\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1As0.99P0.01\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1As0.9P0.1\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1Sb0.01As0.99\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1Sb0.14As0.86\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga1Sb0.25As0.75\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1Sb0.35As0.65\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga1Sb0.3As0.7\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1Sb0.85As0.15\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga1Sb0.8As0.2\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga1Sb0.95As0.05\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga1Sb0.99As0.01\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga2(TeO3)3\\n\",\n        \"output\": \" 4.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga2Cu1S3.5\\n\",\n        \"output\": \" 2.42\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ga2CuSe4\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga2GePbSe6\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga2GeTe3\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga2HgS4\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga2HgSe4\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga2NiS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga2PbS4\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga2PbSe4\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga2S3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga2Se2O7\\n\",\n        \"output\": \" 4.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga2Si(AgS3)2\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga2SiPbSe6\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga2SnGeS6\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga3CuTe5\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ga3Pt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga3SiAg3Se8\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga4Cu2Te7\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga4PbS7\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga4SnS7\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga4SnSe7\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga5Ge(PbS3)4\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga5Ge(PbSe3)4\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ga5Pd13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ga8Cu3Mo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ga9Rh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"GaAgGe3Se8\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaAgGe5Se12\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"GaAgGeS4\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaAgO2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaAgTe2\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaAs2W\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaBi\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GaBi25O39\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"GaCuGeSe4\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"GaCuO2\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GaFe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"GaFeNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaGeTe\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"GaHSeO4\\n\",\n        \"output\": \" 5.51\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"GaP\\n\",\n        \"output\": \" 2.74\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaSiAgSe4\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GaSiRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GaTc\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GaTc2W\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Gd(CuS)3\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Gd(CuSe)3\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd(CuTe)3\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Gd(InS2)3\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd(NiGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Gd(SiRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Gd1.05Sc0.95Se3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd1.47Mn2.04In0.49S5\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Gd1.87Lu2.13Se6\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd1Mn1.95In1.05S5\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Gd2(Zn2Ge)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Gd2AlCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Gd2Mn4S7\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Gd2O3\\n\",\n        \"output\": \" 5.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Gd2S3\\n\",\n        \"output\": \" 2.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd2Se3\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd2Te3\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd2Zn17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Gd2ZrS5\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Gd3(AlNi3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Gd3.04Sc0.96S6\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Gd3Al0.74Si0.7S7\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Gd3Al7Ag2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Gd3Co11B4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Gd3ReO7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Gd3S4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Gd4GaSbS9\\n\",\n        \"output\": \" 2.41\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Gd6Ge2.5S14\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Gd6Ta4Al43\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GdAs\\n\",\n        \"output\": \" 0.63\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GdB(SbO4)2\\n\",\n        \"output\": \" 3.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GdB6\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GdB66\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GdCd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GdCd4B3O10\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GdGeRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"GdH2NO5\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GdInIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GdN\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GdNiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GdO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GdPbAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GdSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"GdSbPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GdScS3\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"GdSe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GdTe\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GdZn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GdZnIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge(Bi3O5)4\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge(SeO3)2\\n\",\n        \"output\": \" 5.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge(WO3)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge0.01Pb0.99Se1\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge0.01Te0.01Pb0.99Se0.99\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.01Te0.99Pb0.99S0.01\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge0.01Te1Pb0.99\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.02Te0.98Pb0.98S0.02\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ge0.03Pb0.97Se0.97S0.03\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ge0.05Pb0.95Se0.95S0.05\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge0.05Pb0.95Se1\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.05Te0.95Pb0.95S0.05\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge0.05Te1Pb0.95\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge0.06Te0.06Pb0.94Se0.94\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.15Pb0.85Se0.85S0.15\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.15Te0.15Pb0.85Se0.85\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge0.15Te1Pb0.85\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge0.1Pb0.9Se0.9S0.1\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ge0.1Pb0.9Se1\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge0.1Te1Pb0.9\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ge0.25Te1Pb0.75\\n\",\n        \"output\": \" 0.44\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.2Pb0.8Se1\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge0.2Te0.2Pb0.8Se0.8\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge0.2Te1Pb0.8\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.39Te1Pb0.61\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge0.3Pb0.7Se1\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ge0.3Te1Pb0.7\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge0.41Te1Pb0.59\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ge0.4Te1Pb0.6\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge2Os\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge2Sb2Te5\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ge3Bi3O10.5\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ge3Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ge40Te5.3I8\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ge5(Te4As)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"GeAs3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GeI2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GeO2\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GeP\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"GePb2(SeO3)4\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"GePbS3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"GePt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"GeRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"GeTe2\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"H2Se\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"H7Se2NO6\\n\",\n        \"output\": \" 4.81\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HPbI3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf(CoSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf(CuP)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf(VGa2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hf(VH2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf2Al3C4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf2Co4P3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf2Fe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf2Ge\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hf2Hg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf2MnIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hf2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf2OsPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hf2ReRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hf2S\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf2Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hf2Tl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf3(CuSi)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hf3(NiGe)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hf3P\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf3P3Pd4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hf3Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hf3Zn3N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hf4Al3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hf4Co4Si7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hf54Os17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hf5CuPb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hf5Pb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf5Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf5Sb9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hf5Si4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hf5Sn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hf5Sn4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hf5Te4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hf6PbO18\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hf7P4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HfAlPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfAs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfAsRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HfB\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfB4Ir3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HfC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HfCo3B2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HfFe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HfGaCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HfHg4(AsCl3)2\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HfHg4(PCl3)2\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HfInCu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HfNi5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HfO2\\n\",\n        \"output\": \" 5.55\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HfOs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HfPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfS2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfSe2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HfSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HfSiPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfTc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HfTiF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfTl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfVSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HfZnNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hg2Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hg2Sb2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hg3As\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hg3Bi2(SCl4)2\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Hg3Bi2(TeCl4)2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hg3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hg3PS3\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hg3PS4\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Hg3Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Hg5AsS2I3\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Hg7.5As4Cl6\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Hg8Bi3As4Cl13\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HgBr\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HgBr2\\n\",\n        \"output\": \" 3.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HgBrCl\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HgCl2\\n\",\n        \"output\": \" 4.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HgI\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HgIrO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HgOsPb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HgPS3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HgPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HgPt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HgRhO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HgS\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HgTe\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HgTeBr\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HgTeI\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ho(BC)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ho(BiO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(CuO2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(CuSe)3\\n\",\n        \"output\": \" 0.16\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(CuTe)3\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ho(InS2)3\\n\",\n        \"output\": \" 1.23\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(MnSn)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(NiB)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ho(SbO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ho(SiOs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(SiPd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(SiPt)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho(SiRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ho10Si17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho2Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ho2B4C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho2Co17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho2CuRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ho2Ge5Rh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho2GeS5\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho2HfS5\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ho2O3\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ho2Pd2Pb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ho2S3\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho3AlC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ho3GaC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ho3Ge5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ho3Hg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho3Ni19B10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho3P\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ho3Pd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ho4C7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ho4Ga16Co3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ho5(Ge5Rh2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ho5Si4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoAlAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoAlB14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoB2Rh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoB4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HoC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HoCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoCd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HoCdCu4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HoCo3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HoCu4Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoGeAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoInAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"HoInPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HoMg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoMgAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoMgZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HoMn12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoNiGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoSb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HoSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoSiRu2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"HoTh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoTiGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HoTiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoTiSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"HoTlPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"HoZnRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"HoZnRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ICl2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In(MoSe)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In(PSe2)2\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.001Te1Pb0.999\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.005Te1Pb0.995\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In0.01Ga0.99As0.99P0.01\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In0.01Ga0.99As1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.01Te1Pb0.99\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In0.04Te1Pb0.96\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In0.07Te1Pb0.93\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.1Ga0.9As0.1P0.9\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.1Ga0.9As0.9P0.1\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.2Ga0.8As0.2P0.8\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In0.2Ga0.8As0.8P0.2\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.2Ga0.8As1\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In0.3Ga0.7As0.3P0.7\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.3Ga0.7As0.7P0.3\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In0.3Ga0.7As1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In0.3Ga0.7P1\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In0.4Ga0.6As0.4P0.6\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.4Ga0.6As0.6P0.4\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In0.4Ga0.6As1\\n\",\n        \"output\": \" 0.81\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.4Ga0.6P1\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.4Ga1.6Cu1S3.5\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.5Ga0.5As1\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In0.5Ga0.5P1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.6Ga0.4As0.6P0.4\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.72Ga0.28As1\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In0.7Ga0.3As0.3P0.7\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In0.8Ga0.2As0.2P0.8\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In0.8Ga0.2As0.8P0.2\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In0.8Ga0.2As1\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.99Ga0.01As0.01P0.99\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.99Ga0.01As0.99P0.01\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In0.9Ga0.1As0.1P0.9\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In0.9Ga0.1As0.9P0.1\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In1.01Cu0.99Se2.01\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In1.05Cu0.95Se2.05\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In1.1Cu0.9Se2.1\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In1.3Cu0.7Se2.3\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In1.5Cu0.5Se2.5\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In1.65Cu0.35Se2.65\\n\",\n        \"output\": \" 1.19\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In1.6Cu0.4Se2.6\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In1.6Ga0.4Cu1S3.5\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In1.7Cu0.3Se2.7\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In1.85Cu0.15Se2.85\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In1.8Cu0.2Se2.8\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In1.99Cu0.01Se2.99\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In1.9Cu0.1Se2.9\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In11.3Bi14.7S38\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In11Cu9Se20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In1Ag1.75Sb5.75Se11\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In1Ga1Cu1S3.5\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In1Hg4As2.5Br3.5\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In1Sb0.01As0.99\\n\",\n        \"output\": \" 0.17\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In1Sb0.1As0.9\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In1Sb0.2As0.8\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In1Sb0.3As0.7\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In1Sb0.4As0.6\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In1Sb0.5As0.5\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In1Sb0.6As0.4\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In1Sb0.7As0.3\\n\",\n        \"output\": \" 0.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In1Sb0.8As0.2\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In1Sb0.99As0.01\\n\",\n        \"output\": \" 0.35\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In1Sb0.9As0.1\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In2As2Cl2O5\\n\",\n        \"output\": \" 4.62\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In2B(PO4)3\\n\",\n        \"output\": \" 5.39\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In2Bi3Se7I\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In2Co\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In2Cu1S3.5\\n\",\n        \"output\": \" 1.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In2FeSe4\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In2GeTe3\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In2Hg6(P2Cl3)3\\n\",\n        \"output\": \" 3.13\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In2HgS4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In2HgSe4\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In2O3\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In2Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In2S3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In2Se2O7\\n\",\n        \"output\": \" 2.97\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In2Te\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In3AgTe5\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In3Au10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In3Bi7(Pb2S9)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In3CuS5\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In3CuSe5\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In3Pd5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In3Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In4As5(BrO4)3\\n\",\n        \"output\": \" 4.22\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"In4Bi3S10\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"In4Cu2Te7\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"In4S5\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In4Se3\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In5AgS8\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In5AgTe8\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In5CuS8\\n\",\n        \"output\": \" 1.34\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"In5Se6\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"In9AgTe14\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"InAg3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"InAgO2\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"InAgTe2\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"InAsI\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"InAu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"InBi2S4Br\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"InBi2S4Cl\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"InBi2Se4Br\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"InCuGeSe4\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"InCuS2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"InFe2CuSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"InHg7S6Cl5\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"InHgW2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"InPS4\\n\",\n        \"output\": \" 3.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"InPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"InPt3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"InSb2S4Br\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"InSb2S4Cl\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"InSb2Se4Br\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"InSiIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"InSiTe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"InSn2As2Se\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"InSnAsSe\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ir0.67S2\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ir0.67Se2\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"IrPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"IrS2\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"IrSe2\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"IrSeS\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K(CoSe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K(FeAs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K(GeSe2)2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K(OsO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K0.8Sn2Hg1.2S8\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K1.25Bi7.25Pb3.5Se15\\n\",\n        \"output\": \" 0.53\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K1.46Sn3.09Bi7.45Se15\\n\",\n        \"output\": \" 0.39\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K1.83Cd1.83Bi2.17S6\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K10Fe4Sn4S17\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K10Mn4Sn4S17\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K10Sn3(PSe3)8\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K10Zn4Ge4S17\\n\",\n        \"output\": \" 3.34\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K11Mn4O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2.15Sb8.15Pb1.7Se15\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2Ag3Sb3S7\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2AgSnSe4\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Al2B2O7\\n\",\n        \"output\": \" 6.89\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2Au(IO3)5\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2B10H9O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2BaNb2S11\\n\",\n        \"output\": \" 1.77\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2Cd(PSe3)2\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Cd2Te3\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2Cd3S4\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Cd3Se4\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2Cd3Te4\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Ce(PO4)2\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Dy2Ti3O10\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2FeGe3Se8\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2Ga3CuSe6\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Gd2Sb2Se9\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Gd2Ti3O10\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Ge2PbS6\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Ge3(BO5)2\\n\",\n        \"output\": \" 5.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2Hg(PSe3)2\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2Hg3(GeS4)2\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2Hg3Se1.31S2.69\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Hg3Se2.97S1.03\\n\",\n        \"output\": \" 2.11\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Ho4Cu4S9\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2In2P3Se10\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2In3AgSe6\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2In3CuSe6\\n\",\n        \"output\": \" 1.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2La2Sb2S9\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2La2Ti3O10\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Mn(SnSe3)2\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Mn3S4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2MnSnSe4\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2Mo2Se2O11\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2NbCuS4\\n\",\n        \"output\": \" 2.82\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2NbCuSe4\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2NbO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Nd2Ti3O10\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2PAuS4\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2PdSe10\\n\",\n        \"output\": \" 1.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2RbSb\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2ReH9\\n\",\n        \"output\": \" 5.71\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2RuCl6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2S\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2Sb8Se3\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Se\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2Sm2Ti3O10\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2SmP2S7\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2Sn(AuS2)2\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2Sn3(SbS5)2\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2Ta15O32\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K2Te\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2TeI6\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2Th(CuS2)2\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2Ti(CuS2)2\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K2VAgS4\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K2VCuS4\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K2Zn(SnSe3)2\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K2ZnTe2\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K3(FeS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K3B6ClO10\\n\",\n        \"output\": \" 6.89\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K3Bi2I9\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K3Cd(BO2)5\\n\",\n        \"output\": \" 3.47\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K3Cr2(PS4)3\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K3Ga3Ge7S20\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K3Ga3Ge7Se20\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K3Hg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K3LiNb6O15\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K3NaSn3Se8\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K3Nb2AsSe11\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K3Sm(AsS4)2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K3Sn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K3Ta2AsS11\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K3Ta2AsSe11\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K3Th2Cu3S7\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K3Ti2P5S18\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K3UF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K3V\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K4(ZrSe5)3\\n\",\n        \"output\": \" 1.81\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K4Ag9(SbS3)4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K4Al4Si19\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K4C2O3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K4Ce3Sn3S14\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K4Ga4Si19\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K4Ge(PSe3)4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K4GeS4\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K4GeSe4\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K4Hf3Se14\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K5In3P6Se19\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K6Cd4Sn3Se13\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"K6CdTe4\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K6Ta1.03Nb2.97S25\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"K6Ta2.93Nb1.07S22\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K6Yb3(PS4)5\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"K8Ce2I18O53\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"K8N3O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"K9Bi13S24\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KAg2AsS3\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KAg2PS4\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KAg2SbS3\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KAg2SbS4\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KAgAsS2\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KAgF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KAgO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KAlGeS4\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KAsSe2\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KAu(IO3)4\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KB5PbO9\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KBaAsSe3\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KBaB5O9\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KBaSbSe3\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KBi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KBi3S5\\n\",\n        \"output\": \" 1.21\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KBiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KBiS2\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KBiSe2\\n\",\n        \"output\": \" 0.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KBr\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KC60\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KCd4Ga5Se12\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KCeSe4\\n\",\n        \"output\": \" 1.54\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KCl\\n\",\n        \"output\": \" 8.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KCoO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KCu2BiS3\\n\",\n        \"output\": \" 1.29\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KCu3S2\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KCu4AsS4\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KCuPO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KCuSnS3\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KCuSnSe3\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KEuAsS4\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KEuS2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KF\\n\",\n        \"output\": \" 10.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KFe2BiO5\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KFeCuTe2\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KGaSe2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KGaSnSe4\\n\",\n        \"output\": \" 1.73\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KH(CN2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KHg11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KIn(TeO3)2\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KInGeS4\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KInS2\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KInSe2\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KInSnS4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KLi(WO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KLiCO3\\n\",\n        \"output\": \" 6.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KLu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KMo6S7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KNb2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KNb2Se\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KNb3(SeO6)2\\n\",\n        \"output\": \" 3.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KNb3(TeO6)2\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KNbSe2O7\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KP(HO2)2\\n\",\n        \"output\": \" 6.95\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KPAu5S8\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KPPbO4\\n\",\n        \"output\": \" 4.44\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KPSe3\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KPSe6\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KRbBi8Se13\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KRuO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KSb\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KSb(SO4)2\\n\",\n        \"output\": \" 4.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KSc(SeO3)2\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KScO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KSi2P3\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KSiBiS4\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KSm2CuS4\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KSnAuS3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KSnAuSe3\\n\",\n        \"output\": \" 2.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KTa3(TeO6)2\\n\",\n        \"output\": \" 4.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KTa3CuO9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KTaO3\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KTbSe4\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KTeP2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KThCuS3\\n\",\n        \"output\": \" 2.95\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KTi2F7\\n\",\n        \"output\": \" 6.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KTi5Se8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KTm\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KUClO3\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KUCuSe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"KV2I3O13\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KV4Ag11O16\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"KV6O11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KY(TeO3)2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"KYb2F7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KYbSe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"KZn4(BO3)3\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"KZrPSe6\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La(FeAs3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La(In2Au)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La(InS2)3\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La(Ni2B)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La(PRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La(SiOs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La(SiRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La1.86Tb1.14Ga1.67S7\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La10Mn9O30\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La10Se14O\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La10Si8O3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La16Mn15O48\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La1Se0.14S1.86\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La2.1Bi5.9Pb2S14\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La20Cu9O40\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La20Mo12Cl4O63\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La2B4Rh5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La2CuO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2Fe(SeO)2\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La2Fe2I\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2Ga0.33Sb1S5\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2Ga2GeS8\\n\",\n        \"output\": \" 2.78\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La2Ge2Se7\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2Ge5Ir3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2Ge5Rh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La2GeSe5\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2HfS5\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La2In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La2Mn(SeO)2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2Nb2N2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La2Ni5B4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2O3\\n\",\n        \"output\": \" 5.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La2PC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La2PI2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La2PdO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2Pr2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La2Rh7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2S3\\n\",\n        \"output\": \" 2.77\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La2Si5Rh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2Sn5Rh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2TiCoO6\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2V2IO9\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2VCoO6\\n\",\n        \"output\": \" 0.41\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2VNiO6\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La2YbCuS5\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La2YbCuSe5\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La2Zn(SeO)2\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La2ZrS5\\n\",\n        \"output\": \" 2.01\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La3(BN2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La3(OsO5)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La3(ReO5)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La3AlN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La3CuGeSe7\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La3Ga1Ge0.5S7\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La3GaCuSe7\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La3Ge3Br2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La3In1Ge0.5S7\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La3LuSe6\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La3Mg0.5Sn1S14\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La3Mo4O16F\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La3NiBr3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La3Si1Sb0.33S7\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La3Si1Sb0.33Se7\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La3Te4\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La3ZrSb5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La4Cd4In2S13\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"La4Co3O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La4Fe(SbS5)2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La4Fe(SbSe5)2\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La4In5S13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La4InSbS9\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"La4InSbSe9\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La5Cu6.33S7O4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La5In3(S3O)3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La5SmS8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La5YbS8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"La6Sb4(SO4)3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"La8Mn7O24\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"La8Sb2S15\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaAl12O19\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaAl4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LaAl4Co\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LaB6\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaBPt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaBeB3O7\\n\",\n        \"output\": \" 5.65\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaBiAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaCd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaCdAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaCdAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaCu6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaCuSO\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaCuSeO\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaCuTeO\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaF3\\n\",\n        \"output\": \" 6.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaGa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaGa3Pd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaGaO3\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LaGaS3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaGeI\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaH2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaH2NO5\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaIn2Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaIn5Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaInS2O\\n\",\n        \"output\": \" 2.73\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaMg(FeO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaMg2H7Pd\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaMg3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaNbN2O\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaP\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaP3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaPd3S4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaPt5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaRe2Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaReB\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaSb\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaScSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LaSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LaSi2\\n\",\n        \"output\": \" 0.19\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaSi2Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaSn3Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LaTaN2O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaTb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaV\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LaVI5O16\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaYbZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LaZnAsO\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LaZnAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li(CuO)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li(NiO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li0.33Ag1Sn0.67O2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li0.33Ti0.67Ag1O2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li11Mn13O32\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li12Fe5O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li13Nb14ZnO42\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li13Ti22O48\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li14Ti21O48\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li15(FeO4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li15Mn2O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li17Nb20O60\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li17Ti20O40\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2(FeO2)5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2(LuGe)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2(NiO2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li23(MnAs)20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2B4O7\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2CdGe\\n\",\n        \"output\": \" 0.99\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2CdGeS4\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2CdSnS4\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Co4O7F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2CrCo3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2CrCuO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Cu2S3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2CuF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2DyIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2EuSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2Fe2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Fe3CoO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2Fe3NiO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2Fe3SnO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2FeGeS4\\n\",\n        \"output\": \" 1.42\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2FeSnS4\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2FeWO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Ga(GeSe3)2\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Ga2GeS6\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2GaPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2HgGe\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2HgGeS4\\n\",\n        \"output\": \" 2.46\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2In2GeS6\\n\",\n        \"output\": \" 3.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2In2GeSe6\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2In2SiS6\\n\",\n        \"output\": \" 3.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2In2SiSe6\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2InAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2LaTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2MgHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2MgIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2MgSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2MnCo3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2MnCu3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2MnGeS4\\n\",\n        \"output\": \" 3.06\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2MnNi3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2MnO2F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Mo2Se2O11\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2Nb2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2NdAs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2NdSb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Ni2SbO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2Ni3TeO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2Ni5(PO4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2PmAl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2PmGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2PrIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2PrP2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2PtO3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2Si4Ni5O14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2SiHgS4\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2Sn5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2SnHgS4\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2SnIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2TeMoO6\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2TeWO6\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2Ti3FeO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2TiMn3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2TlAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2U(MoO5)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li2V2F7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2V3CrO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li2V3FeO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li2YbPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2ZnGe\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li2ZnGeSe4\\n\",\n        \"output\": \" 1.86\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2ZnSnS4\\n\",\n        \"output\": \" 2.87\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li2ZnSnSe4\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3(CoO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3(CuO)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3(CuO2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3AlP2\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li3AlTe4O11\\n\",\n        \"output\": \" 3.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3Bi\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3Co(NiO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3Co2(GeO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Co3SbO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Co4TeO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3Cr(NiO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Cr3(CuO6)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li3CrCo3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li3CrO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Cu4NiO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li3Dy\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li3Fe(CoO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Fe(SbO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3Fe2SbO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li3FeNi3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3FeS3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3FeTe4O11\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li3GaTe4O11\\n\",\n        \"output\": \" 3.85\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li3Mn(CuO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li3Mn(NiO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li3Mn2(CoO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Mn2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Mn2CuO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3Mn3NiO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3Mn3WO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3Mn4(PO4)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3Mn4O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3MnAs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li3Mo2P5O18\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Ni(SbO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3Ni2(GeO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Ni3(PO4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3PS4\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3ScN2\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3Si3Ag2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li3Ti2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3Ti3(PO4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3V12O29\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li3V4FeO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li3V4NiO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li3VOF5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li4(FeO2)9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4.5Al0.5Te1O6\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4.5Cr0.5Te1O6\\n\",\n        \"output\": \" 1.79\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li4.5Fe0.5Te1O6\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4.5Ga0.5Te1O6\\n\",\n        \"output\": \" 4.99\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4.5Mn0.5Te1O6\\n\",\n        \"output\": \" 1.97\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4Co2Ni3O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4Co3CuO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4Co5SbO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4Cr3NiO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4CrO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li4Cu(PO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4Fe2Cu3O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4Fe3NiO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4Fe7(OF7)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4FeNi3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4HgGe2S7\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4MgNi3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4Mn(WO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4Mn3Cr3O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li4Mn5Cu3O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4Mn5Nb3O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li4Mn5NbO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4Mn5Ni3O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4NbNi3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4Ni2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4Ni3BiO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li4Ti5Cr3O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li4TiCr3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4V5Cu3O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li4VF7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li4WO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li5(BiO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li5Co2Ni3O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li5Co2O2F5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li5Cr2Ni5O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li5Fe2Ni3O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li5Fe6(BO3)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li5La3Nb14O42\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li5Mn2Cu5O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li5Mn3(FeO5)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li5Mn5(SbO6)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li5Mn6(BO3)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li6(NiO2)5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li6Fe3Co7O20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li6Fe9CoO20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li6FeNi9O20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li6FeO5F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li6FeO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li6Mn5CoO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li6Mn5FeO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li6Tb2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li7(Mo3S4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li7(NiO2)11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li7Ca8Nb12O40\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li7Ti16O32\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Li7Ti5O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li7Ti7O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li8BiS6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Li8GeN4\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li8IrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li8PO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li8PrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li8Ti16CuS32\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Li8TiNi7O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Li9Fe3(WO4)7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Li9Ga13(Te7O22)3\\n\",\n        \"output\": \" 4.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiAgF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiAl2Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiAl2Tc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiAl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiAlB4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiAlGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiAlRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiAsS2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiB3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiB9PbO15\\n\",\n        \"output\": \" 4.75\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiBePt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiBi2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiBi3(ClO2)2\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiBiS2\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiCa2Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiCa2Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiCa2In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiCa2Mg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiCa3As2H\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiCaO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiCd2Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiCdBO3\\n\",\n        \"output\": \" 4.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiCl\\n\",\n        \"output\": \" 9.33\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiCo(CO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiCo7O7F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiCoS2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiCu2(CO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiCu2Ge\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiCu3F7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiCu5P3O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiCuO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiCuPO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiEr2Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiErAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiEuH3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiF\\n\",\n        \"output\": \" 11.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiFe2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiFe2(SiO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiGa(GeSe3)2\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiGaAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiGaAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiGaO2\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiGaPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiGaPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiGaTe2\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiGd5P2O13\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiGeRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiH3(SeO3)2\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiHf2Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiHfPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiHg2Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiHoAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiHoO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiIn(IO3)4\\n\",\n        \"output\": \" 4.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiIn2Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiInAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiInS2\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiInSe2\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiInSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiInSnS4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiInTe2\\n\",\n        \"output\": \" 1.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiLa2IrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiLu2Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiLu2Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiLu2Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiLu2Tc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiMg2Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiMgAs\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiMgBi\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiMgN\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiMgSnPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiMn(PO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiMn2(PO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiMn4O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiMn9Se10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiMnCoO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiMnCuO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiMnO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiMnP2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiMnSiO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiMo3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiMoIO6\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiNb3(BiO3)4\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiNi2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiNiP2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiPm2Al\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiPm2Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiPm2Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiPm2Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiPr2Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiSb3PbS6\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiSbS2\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiSbSe2\\n\",\n        \"output\": \" 0.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiSbTe2\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiScHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiSiB6\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiSiPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiSiRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiSm3SiS7\\n\",\n        \"output\": \" 2.83\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiSn(PO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiSn4Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiSnAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiTa3(BiO3)4\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiTaO3\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiTaRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiThAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiTi11O20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiTi3O6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LiTiSiO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiTlPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiTm2Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiTm2Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiTmSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiV2NiO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiV3O4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiY(CuP)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LiY2Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiYbF4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiYbPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiZn(Fe5O8)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiZn2GaO4\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiZnBO3\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LiZnN\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LiZr2Os\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LiZrRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Lu(InS2)3\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Lu(SiOs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Lu2AgAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Lu2Al3Co\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Lu2AlTc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Lu2CdAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Lu2CdIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Lu2CrS4\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Lu2Fe2Si2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Lu2FeS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Lu2InHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Lu2MgHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Lu2Mn12P7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Lu2Mo2C3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Lu2O3\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Lu2TlAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Lu2TlCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Lu2TlCu3Se5\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Lu3BC3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Lu3Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Lu3InN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Lu3TlC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Lu4C7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Lu5(Si5Ir2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Lu5Si3B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Lu7(NiTe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Lu7(TePd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LuAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LuAl2Pd5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LuAlAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LuAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LuBPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LuC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LuCd4B3O10\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LuCdAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LuGaRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LuGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LuHfRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LuIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LuIr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LuMnSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LuNiBC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LuP\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"LuPt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LuScRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LuScRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"LuScZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"LuSi2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"LuSiIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LuU2S3O2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"LuUO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg(As2Rh3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg(CoS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg(FeO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg(FeS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg(SnO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg(TiS2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg10B16Ir19\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg17Al11Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg23Al30\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg2AgIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg2Co\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg2CrN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg2Cu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg2CuWO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg2Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg2Ge\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg2GeB2Rh5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg2GeSe4\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg2MnN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg2PdAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg2RhAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg2Si\\n\",\n        \"output\": \" 2.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg2SiPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg2TcO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mg2TiIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg2V9O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg2Zr14O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg3(B25C4)2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg3(MnAl9)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mg3(Ni10B3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg3(Ni10P3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg32Al36Ag13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg3Al9FeSi5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg3AsN\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg3Bi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg3Ga7Co2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg3Ge\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg3N2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mg3P2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg3Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg3Ru2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg3Sb2\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg3Tl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg4Sc3(SiO3)8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg5As\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mg5B3O9F\\n\",\n        \"output\": \" 5.63\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mg5Ti13O30\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mg5Tl2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mg9CuO10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MgAgAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MgCo2(PO5)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MgCr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgCu2GeS4\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgCu2SiS4\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MgCuBi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MgCuSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MgCuSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MgF2\\n\",\n        \"output\": \" 11.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MgIn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MgInAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MgInPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MgMnO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MgMnRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MgNiSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MgPb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MgPt5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgRh2Pb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MgRhF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgSbF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MgSbPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MgSc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MgScAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MgSi7Ir3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgSiN2\\n\",\n        \"output\": \" 4.05\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MgSnRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgTe\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MgTi11O20\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgTi4O6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MgTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MgV4O6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MgZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn(BW)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn(CoO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn(PbO2)2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn(SbO2)2\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mn(SbO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn(SbSe2)2\\n\",\n        \"output\": \" 0.31\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mn0.05Te1Pb0.95\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mn0.1Te1Pb0.9\\n\",\n        \"output\": \" 0.49\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn15Si26\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mn2AlB2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn2AlO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mn2CoAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn2CoGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mn2Cu(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mn2GaW\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn2GeS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mn2Hg5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mn2Nb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mn2OF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mn2P\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn2Tl2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn2VSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mn3(OF3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn3Al10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mn3Cr3(CoO8)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mn3Cr3(TeO8)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mn3NbO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Mn3NiN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn3PdN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mn3PtN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn3SbO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn3V2(SiO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Mn5As4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn5Ge2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mn5O3F5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mn5O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mn7O7F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MnAl3\\n\",\n        \"output\": \" 0.58\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MnAlAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MnAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MnBe2Co\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnCdO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnCoSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MnCu2Sn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MnCu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnF2\\n\",\n        \"output\": \" 9.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnFeAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnFeCoGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnGaNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MnGaPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnGePd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MnGeRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnIn2PbS5\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnInCu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MnNbO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnNi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"MnNiP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnO\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnO2\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MnP2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnP4\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnPSe3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnS\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MnSb3(PO4)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MnSbPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnSbRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnSe\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"MnSi\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnSiNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MnSnRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnTcOs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MnTe9\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"MnTePd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"MnV(TeO4)2\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Mo2NCl8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mo3Pd2N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Mo5As4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Mo5O14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"MoSe2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na(GeP)3\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na0.5Ge1Pb1.75Se4\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na0.75Eu1.625Ge1Se4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na10(Ga2Sn)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na11Bi5O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na11Ti20O40\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na15Sn4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na19Zr11S30\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2B6O9F2\\n\",\n        \"output\": \" 7.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2Be4B4O11\\n\",\n        \"output\": \" 7.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2Cd(GeSe3)2\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2CdSnS4\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2Cl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na2Cr7O14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2EuGeSe4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2Ga2GeS6\\n\",\n        \"output\": \" 3.29\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na2Ga2SnS6\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na2Gd(PO4)2\\n\",\n        \"output\": \" 4.19\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2Ge2Se5\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2Hg3(GeS4)2\\n\",\n        \"output\": \" 2.68\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2Hg3Se1.49S2.51\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2In2GeS6\\n\",\n        \"output\": \" 3.17\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na2In2GeSe6\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2In2SiS6\\n\",\n        \"output\": \" 3.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2In4Se6S\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2In5Au6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2LiTa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2Mo2Se2O11\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2Nb4Se4O19\\n\",\n        \"output\": \" 3.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2Pt(IO3)6\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na2S\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na2SO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na2Se\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na2Si2Hg3S8\\n\",\n        \"output\": \" 2.86\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na2Sn2Hg3S8\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2Te\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2TeS3\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2TeSe3\\n\",\n        \"output\": \" 1.87\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2Ti2Sb2O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2Ti3O7\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na2Tl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2UI6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2V6O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na2VCuF7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na2Zn(GeSe3)2\\n\",\n        \"output\": \" 2.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na2Zn(SnS3)2\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na2Zn3(SeO3)4\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na3(WO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na3In2Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na3Mn2(GeO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na3MoClO4\\n\",\n        \"output\": \" 4.69\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na3MoO4F\\n\",\n        \"output\": \" 4.77\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na3Re\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na3Sn2ClF6\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na3Tl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na3UF7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na3WClO4\\n\",\n        \"output\": \" 4.99\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na3Zn(BO2)5\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na4Al4Si19\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na4Eu(GeS3)2\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na4Mg(GeSe3)2\\n\",\n        \"output\": \" 2.53\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na4Mg(SiSe3)2\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na5Cu7O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na5Fe6(SiO3)12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na5Gd(MoO4)4\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na6CoSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na6FeS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Na7(CoO3)2\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na7.36Ga7.24Sn4.78Se24\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Na8(CuO2)5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Na8Hg3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na8NbO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Na8PO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Na9(WO3)16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaAlGeS4\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaAsO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaB15\\n\",\n        \"output\": \" 0.32\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaBi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaBiS2\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaBiSe2\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaCd2Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaCd4P3\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaCdAsS3\\n\",\n        \"output\": \" 2.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaCdO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaCdSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaCeS2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaCeS3\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaCuO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaEuO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaF\\n\",\n        \"output\": \" 10.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaFe2(SiO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaFe2O3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaGaGe3Se8\\n\",\n        \"output\": \" 2.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaH3(SeO3)2\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaIn(IO3)4\\n\",\n        \"output\": \" 4.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaIn(TeO3)2\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NaIn3S5\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaIn3Se5\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaInS2\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaInSe2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NaInSnS4\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaInTe2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NaIrPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaLa2TaO6\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaLaS3\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NaLi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaLu(Pd3O4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaNb2PS10\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaNi2O3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaSb\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaSb(PS3)2\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaSbF6\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NaSbTe2\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaSc(SeO3)2\\n\",\n        \"output\": \" 5.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NaSi2Pd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaSm(PS3)2\\n\",\n        \"output\": \" 2.54\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaSn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NaTa3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaTi5Se8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NaY(Te2O5)2\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NaYb(PS3)2\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NaZr2TiF11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NaZrCuTe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nb(Cl2O)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nb17Ir3S40\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nb2(CoO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nb2AgPS10\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nb2Cr4Si5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nb2O5\\n\",\n        \"output\": \" 3.08\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nb2Pb2Se4O15\\n\",\n        \"output\": \" 2.79\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nb2Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nb2Tl3CuSe12\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nb2Tl4S11\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nb3(Fe10B3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nb3B2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nb3Bi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nb3CuO8\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nb3In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nb3IrSe8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nb3Os\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nb3Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nb3Te\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nb3V(PO4)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nb3VS6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nb40N21O16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nb4Co2PdSe12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nb5Ga4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nb5Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nb5OF14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nb6Co7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nb6VSb3O25\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbAg2(PS4)2\\n\",\n        \"output\": \" 2.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbCrN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbCrW\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbCu3Se4\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbCuO3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NbGaCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NbHO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NbHg3F6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbOsPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NbPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbRu2Cl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NbSe2\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NbSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbSiIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NbSnIr\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd(Al4Co)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd(AsPd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nd(CoGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd(CoSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd(CrSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd(GePt)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd(InS2)3\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd(NiSn)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd(PRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd(Re2Si)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nd(SiIr)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd1.33Lu0.67S3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd10Se14O\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd2(SnSe3)3\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd2BC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd2CdIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nd2Fe14B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nd2Ge5Rh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nd2HfS5\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd2IrPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd2Ni7P4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nd2O3\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nd2Ru2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd2S3\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd2Se3\\n\",\n        \"output\": \" 1.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd2Te3\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Nd2WC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd2ZnGa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nd2ZrS5\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd3(GeRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd3AlC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nd3Ge5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd3In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd3Ni13B2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd3Te4\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd3Zr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd4(GeS4)3\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd4Ge3Rh4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Nd4InSbSe9\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nd4Mg3Co2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nd4MgRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Nd4O3F7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Nd5Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Nd5Ge4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdAgAs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdAgPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdAl4Ge2Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdAl7Au3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NdAs\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdAu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdB6\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdBRh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdBi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdCrGe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdCu3(RuO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdCuSO\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdCuTeO\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NdErTl2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdErZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdF3\\n\",\n        \"output\": \" 6.15\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdFeSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdGa2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NdGaO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdIn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdIn5Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdInAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdInCu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdLuSe3\\n\",\n        \"output\": \" 1.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdMg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdMg2Ni9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NdMgNi4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdMnSbO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdMoO4F\\n\",\n        \"output\": \" 3.66\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdNiC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdSbPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NdScGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NdSmHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdSn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NdSnRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NdTe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdTe2\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdTiGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdTlAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"NdTlPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NdZn2Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ni(CN)2\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ni(PO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ni23B6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ni2Ge\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ni2Mo3N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ni2Mo4C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ni2Mo4N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ni2PO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ni2Te3O8\\n\",\n        \"output\": \" 3.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ni3Ge\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ni3Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ni3S4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ni3SnN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ni4(BiO2)9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ni4(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ni7(P2O7)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NiAgO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NiAsO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NiCO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NiGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"NiGePt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NiI\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"NiN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NiO\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"NiS2\\n\",\n        \"output\": \" 0.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"NiTe\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"OsS2\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"P2H12N7Cl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"P2H4RhO9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"P2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"P2Os\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"P2Pd\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"P2Pd3S8\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"P2Rh\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"P2Se3\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"P2Se5\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PH2NO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PH6NO4\\n\",\n        \"output\": \" 6.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PHPbO3\\n\",\n        \"output\": \" 3.97\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"POsS\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"POsSe\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PPdS\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PPdSe\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PRuS\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PSe\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PW5O17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pb17(Cl9O4)2\\n\",\n        \"output\": \" 3.44\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pb1Se0.01S0.99\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pb1Se0.5S0.5\\n\",\n        \"output\": \" 0.33\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pb1Se0.95S0.05\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pb1Se0.99S0.01\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pb1Se0.9S0.1\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pb2O3\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pb2SeN2O9\\n\",\n        \"output\": \" 3.76\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pb3O4\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pb3Se2(BrO3)2\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PbN6\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PbSeO4\\n\",\n        \"output\": \" 4.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pd(IO3)2\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pd16S7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pd2N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pd3(PbS)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PdO\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PdPb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PdS\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PdS2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PdSe\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PdSe2\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pm2CuGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pm2IrRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pm2NiRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pm2PtAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pm3I\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PmCd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PmCdPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PmDy3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PmGaAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PmHgAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PmMgAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PmMgCd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PmMgRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PmSbRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PmSnRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pr(BRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pr(BiO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr(CoAs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr(CoGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr(FeSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pr(InS2)3\\n\",\n        \"output\": \" 1.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pr(MnSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pr1.29Lu0.71S3\\n\",\n        \"output\": \" 1.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pr10Se14O\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pr1Te1.9\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pr27Se40\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pr2Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pr2CdSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pr2Co12P7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pr2Ge2Se7\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr2GeSe5\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr2HgPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr2InGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pr2InPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr2Ir2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr2S3\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr2Se3\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pr2Te4O11\\n\",\n        \"output\": \" 3.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Pr3(Al2Si3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pr3Cd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr3I\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pr4InSbSe9\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr4MgRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr4Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr4Te7\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pr5In11Ni6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr5Si4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr6Fe13Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Pr7Mn8O24\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pr9(SbO)5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PrAgAs2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PrAl3Ni2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrAs\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrB4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PrB6\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PrBN2\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrBPt4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrCo4B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrCuSO\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrErIn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrErMg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrFeGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrGaAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PrGe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrGe5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrGeAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrIn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PrInAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrIr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PrLuIn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PrLuSe3\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrMgAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrMgGa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrMo3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrMoO4F\\n\",\n        \"output\": \" 3.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PrNiGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrO\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PrP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PrSb\\n\",\n        \"output\": \" 0.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PrSbPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrSm3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrSmO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrTaN2O\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PrTl2InSe4\\n\",\n        \"output\": \" 0.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"PrTlSe2\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PrTmTl2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"PrZn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Pt0.97S2\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Pt3Pb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Pt3PbC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"PtN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"PtS2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"PtSe2\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb1.45Sb7.45Pb3.1Se15\\n\",\n        \"output\": \" 0.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb1.54Cd1.54Bi2.46S6\\n\",\n        \"output\": \" 1.33\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb15Hg16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb28(Mg3In17)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2AgPS4\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2BaNb2Se11\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb2Cd(IBr)2\\n\",\n        \"output\": \" 3.35\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb2Cd(PSe3)2\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2Cd3(B4O7)4\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2Cd3S4\\n\",\n        \"output\": \" 2.92\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2Cd3Se4\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2Cd3Te4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb2CrF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb2Cu2Sb2S5\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb2Cu2SnS4\\n\",\n        \"output\": \" 2.08\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb2FeI4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb2GeB4O9\\n\",\n        \"output\": \" 5.54\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb2Hg(PSe3)2\\n\",\n        \"output\": \" 2.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb2Hg3(GeS4)2\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb2Mo3Se3O16\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb2Mo9Se10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb2Na2IrO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb2NaNiF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb2NaVF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb2NbCuS4\\n\",\n        \"output\": \" 2.64\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb2NbCuSe4\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb2PS5\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb2Pt(IO3)6\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb2SCl6F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb2Sn2Hg3S8\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2Sn3(SbS5)2\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb2Tb3AlF16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2Te\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb2TeBr6\\n\",\n        \"output\": \" 2.14\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb2TeI6\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb2Ti(AgS2)2\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb2Ti(CuS2)2\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb2VAgS4\\n\",\n        \"output\": \" 1.83\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb2VCuS4\\n\",\n        \"output\": \" 1.85\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb2Zn3(SeO3)4\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb3(Cu4S3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb3Ag9(PS4)4\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb3Al3Ge7S20\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb3Al3Ge7Se20\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb3Bi2Br9\\n\",\n        \"output\": \" 2.62\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb3Cd(BO2)5\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb3Ga\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb3Li4(BO2)7\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb3Mn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb3Na(MoO4)2\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb3Nb2AsSe11\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb3Sb\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb3Sb2Br9\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb3Sb2I9\\n\",\n        \"output\": \" 1.94\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb3Sm\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb3Ta2AsS11\\n\",\n        \"output\": \" 2.21\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb3Tm\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb3Zn(BO2)5\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb4Ag9(SbS3)4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb4CuSi2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Rb4Ga4Si19\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb4Ge(PSe3)4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb4Ge3B6O17\\n\",\n        \"output\": \" 5.42\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb4Mo5(PO11)2\\n\",\n        \"output\": \" 3.51\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb4Ti3S14\\n\",\n        \"output\": \" 1.59\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb5(W4O15)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb5(WO3)18\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rb5B(SO4)4\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb5Li6(BO2)11\\n\",\n        \"output\": \" 6.53\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rb5Tl3O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rb6O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb7Th2(P2Se7)3\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rb9Bi13S24\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbAg2SbS4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbAg2TeS6\\n\",\n        \"output\": \" 2.04\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbAg5(PS4)2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbAgF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbB5(H2O3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbBa2(PO3)5\\n\",\n        \"output\": \" 7.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbBi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbBi3TeSe4\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbBr3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbC8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbCaBO3\\n\",\n        \"output\": \" 3.67\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbCd(BO2)3\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbCd13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbCd4Ga5S12\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbCd4Ga5Se12\\n\",\n        \"output\": \" 2.19\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbCd4Ga5Te12\\n\",\n        \"output\": \" 1.64\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbCd4In5Se12\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbCu(SbS2)2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbCu2AsS3\\n\",\n        \"output\": \" 1.96\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbCu2SbS3\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbCu4AsS4\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbCuPdF5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbCuSnS3\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbCuSnSe3\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbEuO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbF\\n\",\n        \"output\": \" 10.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbGaSnSe4\\n\",\n        \"output\": \" 1.88\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbGe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbGeB3O7\\n\",\n        \"output\": \" 5.58\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbH2(IO3)3\\n\",\n        \"output\": \" 4.07\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbH3(SeO3)2\\n\",\n        \"output\": \" 4.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbHg3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbHgSbTe3\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbIn4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbIn5S6\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbInGeS4\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbInS2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbInSnS4\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbInTe3O8\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbLiCO3\\n\",\n        \"output\": \" 6.28\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbMn4Ga5Te12\\n\",\n        \"output\": \" 1.53\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbMn4In5Se12\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbMnTe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbMoPO6\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbNa2NiO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbNa2Sb\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbNb3(TeO6)2\\n\",\n        \"output\": \" 3.49\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbNb4Br11\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbNbSe2O7\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbPPbO4\\n\",\n        \"output\": \" 4.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbPSe6\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbPdF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbSbO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbSbSe2\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbSbTe2\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbSc(SeO3)2\\n\",\n        \"output\": \" 4.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RbTa3(TeO6)2\\n\",\n        \"output\": \" 3.88\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbTbSe2\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbTiBr3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbTmO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbU2SbS8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RbUAgS3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbV(CuS2)2\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbVP2S7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbWO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RbY(TeO3)2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbYbZnSe3\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RbZn4In5Se12\\n\",\n        \"output\": \" 1.76\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RbZrPSe6\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Re(TeCl6)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Re2PbO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Re2RuBr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Re2W3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Re3As7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Re3F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Re3P4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Re5(NiAs6)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ReBiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ReCl4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ReF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ReIr3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ReO3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ReOsRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RePO5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ReSi2\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ReSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Rh0.67S2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rh0.67Se2\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Rh2S3\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Rh3Pb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Rh7(PbO5)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RhS3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RhSe2\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"RhSe3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"RhSeS\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ru3Cl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"RuCl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"RuS2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"RuSe2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sb2I2F11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sb2Os\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sb2PbSe4\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sb2Ru\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sb2Te\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sb2XeF14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sb3IO4\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sb4Pb4S11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sb5IO7\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sb6Pb4Se13\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sb6Pb6Se17\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sb8I2O11\\n\",\n        \"output\": \" 2.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SbAs\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SbOsS\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SbOsSe\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SbPb2S2I3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SbPbBrO2\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SbPbIO2\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SbPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SbPt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SbRh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SbRuSe\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SbSBr\\n\",\n        \"output\": \" 2.17\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SbSeBr\\n\",\n        \"output\": \" 1.84\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SbTeI\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SbTeOs\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SbTeRh\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SbTeRu\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc(CuSe)3\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sc(GaFe)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sc(TiN)9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sc(VGa2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sc11(AlGe4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sc14Cu14O37\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sc2(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc2Al3Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sc2CuRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sc2Fe\\n\",\n        \"output\": \" 0.77\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc2FeB2Ir5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sc2GaAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sc2GaIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sc2MnC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sc2S3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sc2TlTc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc3(MnGa3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sc3(ReSi2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sc3BPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sc3C4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sc3Fe2Si3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc3GaC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sc3PbC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc4Ge6Rh7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sc5Bi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc5NCl8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sc5Pb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sc6FeSb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sc6NiTe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sc6Te2Os\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sc7CI12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sc8Te3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ScAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScAg(PSe3)2\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ScAgO2\\n\",\n        \"output\": \" 3.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScAlNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScBIr3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ScBPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScBe5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScCd\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScCdAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ScCdHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScCoGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScCoO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScCrO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScCu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScCuO2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScGa2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ScHg\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ScIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScN\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScNiSb\\n\",\n        \"output\": \" 0.11\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScPPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScRh3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ScSbPd\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScSbRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ScSbRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ScSi3Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ScSnPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScTa2NO5\\n\",\n        \"output\": \" 2.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ScTiNbO6\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScTiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ScTlS2\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScTlSe2\\n\",\n        \"output\": \" 0.79\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ScTlTe2\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ScZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScZn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ScZnNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ScZnPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SeS\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Si(Bi3O5)4\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Si0.001Ge0.999\\n\",\n        \"output\": \" 0.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si0.03Ge0.97\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Si0.0645Ge0.9355\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Si0.07Ge0.93\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si0.08Ge0.92\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Si0.109Ge0.891\\n\",\n        \"output\": \" 1.13\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si0.12Ge0.88\\n\",\n        \"output\": \" 0.84\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si0.162Ge0.838\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Si0.1Ge0.9\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Si0.226Ge0.774\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si0.2Ge0.8\\n\",\n        \"output\": \" 0.86\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Si0.347Ge0.653\\n\",\n        \"output\": \" 1.91\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Si0.3Ge0.7\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Si0.458Ge0.542\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Si0.4Ge0.6\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Si0.6Ge0.4\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Si0.7Ge0.3\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Si0.8Ge0.2\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si0.94Ge0.06\\n\",\n        \"output\": \" 1.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si0.98Ge0.02\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Si0.999Ge0.001\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Si0.9Ge0.1\\n\",\n        \"output\": \" 1.04\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Si15(TeP2)4\\n\",\n        \"output\": \" 1.24\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Si2Ni6B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Si2NiP3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Si2Pd9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Si2Ru\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Si2SbO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Si3N4\\n\",\n        \"output\": \" 5.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SiAs2\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SiAu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SiB3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SiBi3O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SiGe\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SiHg3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SiP\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SiP2\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SiSb\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SiSb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SiSe2\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SiSn\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SiTe2Os\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SiW3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm(BOs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm(CoSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm(CuO2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm(CuS)3\\n\",\n        \"output\": \" 1.82\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm(CuTe)3\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm(ErSe2)3\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sm(InS2)3\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm(MnGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm(NiSn)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm(SiAg)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm(SiNi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm1.82Lu2.18Se6\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm2(PPt2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm2(SnSe3)3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm2AgRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm2AlCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm2Cu4Sn5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm2CuAs3O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm2Fe17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sm2IO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm2In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm2IrPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm2Mn3(SbS3)4\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sm2Mo2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm2O3\\n\",\n        \"output\": \" 5.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm2Pd2Pb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm2RuAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm2S3\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm2Sc3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm2Se3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm2Te3\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm2Tl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm2TlHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sm2TlZn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm2ZrSe5\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm3(Sb7Te12)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm3Al\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm3Al0.33Si1S7\\n\",\n        \"output\": \" 2.26\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm3AlN\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm3B(SO)3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sm3OsO7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm3Sc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sm3Te4\\n\",\n        \"output\": \" 0.51\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm3Zr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm4Al23Ni6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm4GaSbS9\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sm4In21Pd10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm4InSbS9\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sm4MgRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sm4U4O17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sm5Br11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sm6Br13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SmAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmAlCu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmAs\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmAs2Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmAu3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmB(SbO4)2\\n\",\n        \"output\": \" 3.54\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmB6\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SmB66\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SmBPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmBiW2O9\\n\",\n        \"output\": \" 3.39\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SmC10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmCdHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmCo3B2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmCoC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmCrGe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SmCuO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SmCuSO\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmCuSe2\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmCuSeO\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmCuSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SmErMg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmHg3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmHgPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SmHoHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmHoZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SmIn2Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmInAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmLuTl2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmMg3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmMgHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmNi2B2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmNiAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SmNiC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SmP\\n\",\n        \"output\": \" 1.09\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmPbAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmS\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmSb\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmSb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmSe\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmSi3Pt5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmSnPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SmSnRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SmSnTe2\\n\",\n        \"output\": \" 0.52\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmTh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SmTmZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn(PO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn0.001Pb0.999Se1\\n\",\n        \"output\": \" 0.24\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sn0.01Te1Pb0.99\\n\",\n        \"output\": \" 0.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn0.03Pb0.97Se1\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sn0.03Te1Pb0.97\\n\",\n        \"output\": \" 0.21\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn0.05Pb0.95Se1\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sn0.06Pb0.94Se1\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn0.06Te1Pb0.94\\n\",\n        \"output\": \" 0.28\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn0.07Pb0.93Se1\\n\",\n        \"output\": \" 0.08\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn0.08Pb0.92Se1\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn0.08Te0.08Pb0.92Se0.92\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn0.08Te1Pb0.92\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sn0.13Pb0.87Se1\\n\",\n        \"output\": \" 0.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn0.15Pb0.85Se1\\n\",\n        \"output\": \" 0.13\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn0.15Te0.15Pb0.85Se0.85\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn0.17Pb0.83Se1\\n\",\n        \"output\": \" 0.04\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sn0.17Te1Pb0.83\\n\",\n        \"output\": \" 0.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn0.1Te1Pb0.9\\n\",\n        \"output\": \" 0.16\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sn0.23Te1Pb0.77\\n\",\n        \"output\": \" 0.04\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sn0.25Pb0.75Se1\\n\",\n        \"output\": \" 0.04\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn0.25Te1Pb0.75\\n\",\n        \"output\": \" 0.04\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn0.28Te0.28Pb0.72Se0.72\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sn0.2Pb0.8Se1\\n\",\n        \"output\": \" 0.06\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn0.2Te0.2Pb0.8Se0.8\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn0.2Te1Pb0.8\\n\",\n        \"output\": \" 0.08\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sn0.35Te0.35Pb0.65Se0.65\\n\",\n        \"output\": \" 0.09\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sn0.99Te1Pb0.01\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn1Se0.01S0.99\\n\",\n        \"output\": \" 1.08\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn1Se0.2S0.8\\n\",\n        \"output\": \" 1.03\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn1Se0.6S0.4\\n\",\n        \"output\": \" 0.98\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn1Se0.75S0.25\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn1Se0.99S0.01\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn2BiSI5\\n\",\n        \"output\": \" 1.32\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sn2S\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sn2SbS2I3\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn2WO5\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sn3As2\\n\",\n        \"output\": \" 0.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn3Ir2Se3\\n\",\n        \"output\": \" 0.43\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn3P3O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sn3Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sn3WO6\\n\",\n        \"output\": \" 2.49\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sn5(BIr3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sn5(BRh3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SnAs3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SnB\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SnCl2\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SnGeS3\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SnHgO3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SnI2\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SnI4\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SnO\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SnO2\\n\",\n        \"output\": \" 3.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SnPt3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SnRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SnS2\\n\",\n        \"output\": \" 2.43\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SnSb3(PO4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SnSe2\\n\",\n        \"output\": \" 1.62\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SnTe\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr(CeS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr(CeSe2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr(CoP)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr(GaAu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr(In4Rh)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr(LaS2)2\\n\",\n        \"output\": \" 2.85\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr(NdS2)2\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr(PrS2)2\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr(RuO3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr(Sb3Ru)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr(YbS2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr0.5Ta1O3\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr10Al4Si6O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr2Be2B2O7\\n\",\n        \"output\": \" 8.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr2Co2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sr2CoReO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr2Cu(ClO)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr2GaCo2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr2GeN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr2HoRuO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr2La2.58Bi5.42S14\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sr2La2Pt1O7.13\\n\",\n        \"output\": \" 2.52\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr2Li2Nb3O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr2MgIrO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr2MgReO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sr2Pr2Pt1O7.07\\n\",\n        \"output\": \" 3.05\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sr2ScSbO6\\n\",\n        \"output\": \" 3.57\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr2SmTaO6\\n\",\n        \"output\": \" 3.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr2TiO4\\n\",\n        \"output\": \" 3.41\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr2V2(SeO5)3\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr2V3Se5O18\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr2YBi2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr2YReO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr2ZnReO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr3(AlSn)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr3(SnIr)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sr3Bi(PO4)3\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr3Co2S2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Sr3Eu(PO4)3\\n\",\n        \"output\": \" 3.99\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr3Ge(SbSe4)2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr3Li4La5O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr3Sb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr3ScNiO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr3Se3ClO8\\n\",\n        \"output\": \" 4.4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr3Ti2O7\\n\",\n        \"output\": \" 3.26\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr4Ga8Ge15\\n\",\n        \"output\": \" 0.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr4Te3(ClO2)4\\n\",\n        \"output\": \" 4.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr4V2(Se2O7)3\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr5Bi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr5Cd2Sb5F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr5Sn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Sr5V3O12F\\n\",\n        \"output\": \" 4.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Sr6Nb7O21\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr7Bi23O40\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr8(MnN3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr8.007Ge2.043Bi7.949Se24\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr8Al7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Sr8Co8O23\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Sr8Fe3N8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrAl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrB2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrB6\\n\",\n        \"output\": \" 3.68\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrBiClO2\\n\",\n        \"output\": \" 3.52\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrCdSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrCrO4\\n\",\n        \"output\": \" 2.45\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrCuBi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrGe2\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrIn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrIn2(GeIr)4\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrIn2Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrIn2Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrIn4Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrIn4Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrLa3MnO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrLaMn2O6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrLi2Sn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrLi4(BO3)2\\n\",\n        \"output\": \" 6.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrMgIn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrMgSnSe4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SrMnGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrNi2(PO4)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrNi5As3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrO\\n\",\n        \"output\": \" 5.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrPb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrPb3Br8\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SrPbO3\\n\",\n        \"output\": \" 1.78\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrRhF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrS\\n\",\n        \"output\": \" 4.76\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrSbAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrSe\\n\",\n        \"output\": \" 4.42\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrSeO4\\n\",\n        \"output\": \" 4.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrSiPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"SrSnO3\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrSnP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"SrTaNO2\\n\",\n        \"output\": \" 1.99\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrTe\\n\",\n        \"output\": \" 3.73\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrTh(PS4)2\\n\",\n        \"output\": \" 3.02\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"SrTl2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrTlHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"SrUS2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrV13O18\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrZnSO\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrZnSb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"SrZr2Nb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ta11(CuO15)2\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ta11(CuO6)5\\n\",\n        \"output\": \" 2.58\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ta22(CuS12)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ta2Mn3O8\\n\",\n        \"output\": \" 1.89\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ta2MoOs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ta2N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ta2Nb3O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ta2O5\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ta2OsW\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ta2PtSe7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ta2TiN3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ta2Tl4S11\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ta2TlO6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ta3B4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ta3P\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ta4AlC3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ta4FeTe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ta4N5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ta5N6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ta6Be15Cu8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ta6Ni16Ge7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ta7Cu3O19\\n\",\n        \"output\": \" 2.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TaAl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TaAlPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TaAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TaBe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TaCoSn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TaCu3S4\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TaF3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TaGaPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TaInNi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TaN\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TaNiB2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TaPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TaPt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TaRh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TaTiFe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TaTlS3\\n\",\n        \"output\": \" 0.78\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TaW3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb(Al2Fe)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tb(AlC)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tb(CoB)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb(CoGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tb(CuSe)3\\n\",\n        \"output\": \" 0.16\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb(CuTe)3\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb(FeP3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb(GePd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tb(GeRh)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb(InS2)3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tb(MnGe)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb(Ni2P)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tb0.52Pr2.48Ga1.67S7\\n\",\n        \"output\": \" 2.61\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb10B7C10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tb11S16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tb2AlCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb2C3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb2EuSe4\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb2GeS5\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb2In16Pt7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb2O3\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb2Sb5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb2SbO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb2Ti3Ge4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tb3(MnC3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb3FeB7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tb3Ge5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb3Ni13B2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tb3ReO7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tb3Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb4Al2O9\\n\",\n        \"output\": \" 4.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tb4GaSbS9\\n\",\n        \"output\": \" 2.44\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tb5Ti5O17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tb5Tl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tb6PbSe10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TbB(SbO4)2\\n\",\n        \"output\": \" 3.53\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TbBRh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbBe13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TbCl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbCu5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TbGa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TbGa2Co3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbGa3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbH2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TbHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbIn2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TbInAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TbInIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbMn5Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TbNi5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TbNiGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbNiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TbP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TbPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TbRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbSb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbSe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbSnAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbTe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbWClO4\\n\",\n        \"output\": \" 4.24\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TbYHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbYbHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TbYbRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TbZn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TbZrSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tc3Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TcB\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TcS2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TcSe2\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Te0.01Pb1Se0.99\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Te0.05Pb1Se0.95\\n\",\n        \"output\": \" 0.26\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Te0.4Se0.6\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Te0.5Pb1Se0.5\\n\",\n        \"output\": \" 0.29\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Te0.5Se0.5\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Te0.6Se0.4\\n\",\n        \"output\": \" 0.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Te0.8Se0.2\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Te0.99Pb1Se0.01\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Te2Au\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Te2Mo(WS2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Te2Mo2WSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Te2Mo3Se4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Te2MoWS2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Te2Os\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Te2Pd\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Te2Pd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Te2Pd3Pb2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Te2Ru\\n\",\n        \"output\": \" 0.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Te2W2SeS\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Te3MoWS\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Te4Mo(WS)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Te4MoW3S4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TeAs\\n\",\n        \"output\": \" 0.74\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TeI\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TeI4\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TeMoSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TeO2\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TePb3Cl4O3\\n\",\n        \"output\": \" 3.79\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TePd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TeSe\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TeWCl9\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Th(Al2Fe)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Th(Al5Fe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Th(FeGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Th(FeSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Th(GePd)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Th(MnGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Th(SiRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Th2CrN3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Th2Fe7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Th2GeSe2\\n\",\n        \"output\": \" 1.98\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Th2In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Th2Se5\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Th3B2C3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Th6Mg23\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ThAl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ThAl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ThAsSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ThBi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ThCrB4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ThFe2SiC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ThHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ThIr5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ThMn4(CuO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ThPSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ThPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ThRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ThRu3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ThS\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ThSO\\n\",\n        \"output\": \" 2.22\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ThSeO\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ThSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ThSi2Ru3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ThTeO\\n\",\n        \"output\": \" 1.45\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ThU8O18\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti(Bi3O5)4\\n\",\n        \"output\": \" 3.09\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ti10O11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ti11O18\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti13S24\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti1C0.9\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ti20(Sb3Se)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ti2AlV\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti2B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ti2BRh6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti2Be17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ti2Cd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti2CoGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti2CoS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti2CuS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti2MnFe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti2NiH\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ti2NiSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti2OsRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti2RePd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti2ReRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ti2ReRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti2Sb(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ti2TcNi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti2TcPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti2ZnS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti3Be\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti3Cu3O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ti3Fe3O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ti3PO7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti3Pt5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti3SnC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Ti4NiBi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti4O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti4ZnO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Ti5(B6O13)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti5Zn4(TeO6)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ti5ZnO7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Ti6H2O13\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Ti9O10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Ti9O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiAl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TiAlAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TiAsRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiAuCl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiBi25O39\\n\",\n        \"output\": \" 3.1\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiBr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiCoGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiCoSb\\n\",\n        \"output\": \" 0.95\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TiCoSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiCr3(PO4)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiFe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TiFe2As\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiFe2Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiFe2Si\\n\",\n        \"output\": \" 0.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiFeH2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiGaIr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TiHgO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiI\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TiMn2Al\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiMn2Ge\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TiNiSb\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TiO2\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TiOs3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiPO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiReN3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiS2\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiS3\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TiSe2\\n\",\n        \"output\": \" 1.55\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TiTc2Sb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiTe2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TiTlPS5\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TiTlS2\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiTlSe2\\n\",\n        \"output\": \" 0.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TiV4CuO12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TiZn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl(Cu3S2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl(MoSe)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl(WO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl0.001Te1Pb0.999\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl0.005Te1Pb0.995\\n\",\n        \"output\": \" 0.48\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl0.01Te1Pb0.99\\n\",\n        \"output\": \" 0.59\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl0.04Te1Pb0.96\\n\",\n        \"output\": \" 0.57\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl0.07Te1Pb0.93\\n\",\n        \"output\": \" 0.54\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tl16O15F17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tl2.35Sb8.65Se14\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tl2BiP2S7\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl2CdTe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tl2Cu2SnS4\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl2GeTe3\\n\",\n        \"output\": \" 0.36\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl2Hg3S4\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl2Hg3Se4\\n\",\n        \"output\": \" 1.57\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tl2Hg3Te4\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl2InGaSe4\\n\",\n        \"output\": \" 2.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl2InGaTe4\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl2Mo7O22\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl2O3\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl2PAuS4\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl2S\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl2Se\\n\",\n        \"output\": \" 0.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl2Te3As2Se\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl2TeBr6\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl2TeI6\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl2TeS3\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl3AsSe3\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl3Cr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl3Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl3Pb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl3Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tl4CdI6\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl4CuTeO6\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tl4In3GaS8\\n\",\n        \"output\": \" 2.63\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tl5Te3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl6Cu(TeO5)2\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tl8Os8O27\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tl9SbSe6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlAgSe2\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TlAgTe2\\n\",\n        \"output\": \" 0.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlAsS2\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlAsSe2\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TlBiTe2\\n\",\n        \"output\": \" 0.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TlBiTe3\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TlCdS2\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TlCoBi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlCoMo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlCr5(Se3S)2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TlCr5(SeS)4\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlCr5(SeS3)2\\n\",\n        \"output\": \" 0.94\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlCr5S8\\n\",\n        \"output\": \" 1.01\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlCr5Se3S5\\n\",\n        \"output\": \" 0.89\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TlCr5Se5S3\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlCr5Se7S\\n\",\n        \"output\": \" 0.71\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlCr5Se8\\n\",\n        \"output\": \" 0.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TlCr5SeS7\\n\",\n        \"output\": \" 0.97\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlCuCl3\\n\",\n        \"output\": \" 2.98\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlCuSe2\\n\",\n        \"output\": \" 1.07\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TlFeI3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlGaS2\\n\",\n        \"output\": \" 3.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TlGaSe2\\n\",\n        \"output\": \" 1.65\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlGaTe2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlHg6S4Br5\\n\",\n        \"output\": \" 3.03\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TlHg6Se4Br5\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlInGeS4\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TlInHgS3\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TlInTe2\\n\",\n        \"output\": \" 0.62\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlN\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlN3\\n\",\n        \"output\": \" 3.58\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlNi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TlPS2\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TlPSe2\\n\",\n        \"output\": \" 0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TlS\\n\",\n        \"output\": \" 1.36\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TlS2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TlSbSe2\\n\",\n        \"output\": \" 0.82\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlSbTe3\\n\",\n        \"output\": \" 0.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TlSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlSnAuSe3\\n\",\n        \"output\": \" 1.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TlTe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TlTeP\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TlZn2Tc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tm(CoSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tm(CuGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm(CuS)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm(CuTe)3\\n\",\n        \"output\": \" 0.14\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tm(FeSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm(GeRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tm(MnGe)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm(NiGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tm(SiOs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tm2AlOs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm2CdHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tm2CuTc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tm2Ga10Os3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tm2In\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tm2IrPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tm2MgRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm2MgTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tm2O3\\n\",\n        \"output\": \" 4.53\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tm2Ru2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tm2ZnAg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tm2ZnGa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tm2ZnHg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tm2ZnOs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm3(GePd)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Tm3GaC\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Tm4In(NiGe2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Tm4Sb2Se11.68\\n\",\n        \"output\": \" 1.22\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Tm5(Ge5Rh2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Tm5Ti5O17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TmAl4Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TmAlCu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TmAs\\n\",\n        \"output\": \" 1.18\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmAu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmB2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmBPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmBRh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TmCdAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TmCoSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmCu4Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmCuSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmH2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TmIn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmLuPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmMg2Sc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmMgAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmMgCd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmMnGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TmMnO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TmPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"TmSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TmScHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"TmSnRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TmSnRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"TmThRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"TmTl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"TmU2S3O2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"U(Al2Fe)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U(BH4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U(CoGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U(CrC)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"U(CuP)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"U(MnSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"U(SiNi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"U11O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"U2(Co7B2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"U2Al3C4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"U2AlCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"U2AlCo3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"U2Cl5O2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"U2Cr30P19\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U2Cu2As3O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"U2MnN3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U2Re2C3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"U2SnRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"U2TeN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U2Ti\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"U2Zn17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"U3Bi4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"U3Cu2Se7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"U3Nb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"U3Ni3Sn4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U3Se4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"U4N7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"U4Re7Si6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"U4S3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"U5Ge3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"U6Co\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"UAl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"UAl4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"UAlNi4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"UAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"UCo4Sn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"UCoSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"UCuP2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"UFe5Si3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"UFeSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"UGa2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"UGa3Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"UGa5Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"UGaNi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"UGeRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"UHg3(TeCl3)2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"UHg4(AsCl3)2\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"UNiSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"UO\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"UO2\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"UP2S7\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"UP2S9\\n\",\n        \"output\": \" 1.41\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"UPt3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"USbSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"USeS\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"USi3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"UVC2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V12P7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V2(OF)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V2Bi4O11\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V2Cd2Te2O11\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V2GaSn2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"V2NO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"V2OsRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V2Pb4(Se2O7)3\\n\",\n        \"output\": \" 3.37\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"V2Sb(PO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V2Si2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"V2TcRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V2Zn3TeO10\\n\",\n        \"output\": \" 2.96\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"V2ZnO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V3(HO2)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"V3Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"V3As2O9\\n\",\n        \"output\": \" 0.76\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"V3Bi(PbO4)3\\n\",\n        \"output\": \" 2.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V3Cd4(TeO5)3\\n\",\n        \"output\": \" 2.66\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V3CrO10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"V3Cu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V3CuO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"V3Pb2Se5O18\\n\",\n        \"output\": \" 3.14\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V3Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"V3Re\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"V3Si\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V3SiNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V4ZnO8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"V5SiB2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"V6AgO15\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"V6PbO11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"V8O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VAg(IO4)2\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"VAg(PSe3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VAg2I3O11\\n\",\n        \"output\": \" 2.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VB2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"VBi(SeO4)2\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VBi24O41\\n\",\n        \"output\": \" 3.25\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"VCo\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"VCu3(PO4)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VCu3S4\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"VFeRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"VFeSb\\n\",\n        \"output\": \" 0.46\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"VGa(TeO4)2\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"VIn(NiO3)2\\n\",\n        \"output\": \" 1.92\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VIr\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"VIr3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"VNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"VNi5(PO4)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VO\\n\",\n        \"output\": \" 0.3\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"VP\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"VP4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"VPO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"VSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"VTc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"VTe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VTeHO5\\n\",\n        \"output\": \" 2.51\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VZn2BiO6\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"VZnRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"W2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"W2N\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"W3O7F\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"WCl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Y(Al2Cu)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y(Al5Fe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y(AlSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y(CrSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y(CuSe)3\\n\",\n        \"output\": \" 0.88\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Y(CuSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y(CuTe)3\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Y(FeSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Y(NiP)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Y(Re2Si)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y(SiPt)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Y(SiRh)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y(SiRu)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Y(TiGa2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Y2AlZn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y2C3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Y2CuO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Y2Fe2Si2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y2Ge2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y2Ge5Ir3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Y2Mo2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Y2O3\\n\",\n        \"output\": \" 5.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Y2ReB6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y2Ru2O7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Y2S3\\n\",\n        \"output\": \" 2.9\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Y2U3O11\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y3(Fe31B7)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Y3Al3NiGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y3Fe29\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Y3GaCo3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Y3GaS6\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y3Ge4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y3Si3Pd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y3Tm\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y4AsSe3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Y4C7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Y4CuTe8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Y4GaSbS9\\n\",\n        \"output\": \" 2.06\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y4US5O3\\n\",\n        \"output\": \" 1.95\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Y6Zn(SiS7)2\\n\",\n        \"output\": \" 2.38\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YAgO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YAlGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YAlPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YAs\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YB2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YB2Rh2C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YB66\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YBi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YCd4B3O10\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YCdHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YCdPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YCdPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YCo2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YCoO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YCu3(WO3)4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YCuO2\\n\",\n        \"output\": \" 3.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YErRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YH2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YH2NO5\\n\",\n        \"output\": \" 4.83\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YIn2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YMg4Cu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YMgAl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YMgCu4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YMgGa\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YMoClO4\\n\",\n        \"output\": \" 3.82\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YMoO4F\\n\",\n        \"output\": \" 3.78\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YN\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YNi4B\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YSbPd\\n\",\n        \"output\": \" 0.27\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YSbPt\\n\",\n        \"output\": \" 0.16\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YScO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YSiNi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YSiRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YTi4(CuO4)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YTiO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YTmCu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YV(BiO4)2\\n\",\n        \"output\": \" 2.09\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YVSeO10\\n\",\n        \"output\": \" 2.7\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YVTeO10\\n\",\n        \"output\": \" 2.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YWO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YZn5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YZnBiO4\\n\",\n        \"output\": \" 1.58\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Yb(Al2Mo)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Yb(AlGa)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb(AlGe)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb(AlSi)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb(CuS)3\\n\",\n        \"output\": \" 1.56\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb(CuSe)3\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Yb(Fe2Ge)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb(Ga4Co)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb(GaS2)2\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb(GaSe2)2\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb(HO)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb(IO3)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Yb(InS2)3\\n\",\n        \"output\": \" 1.31\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb(MnAs)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Yb(SbS2)2\\n\",\n        \"output\": \" 1.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb(SbTe2)2\\n\",\n        \"output\": \" 0.34\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb(SiAg)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb(SiRh)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb11(Ni10C)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb14Ti10O41\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Yb16S29\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb2(ZnGe)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb23Mg4Cu7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb2Ce8O19\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb2EuS4\\n\",\n        \"output\": \" 1.6\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Yb2EuSe4\\n\",\n        \"output\": \" 1.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Yb2Ge2Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb2HgPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb2InPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb2MgS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb2MgSe4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Yb2O3\\n\",\n        \"output\": \" 5.22\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Yb2SmS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb2Sn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Yb2ZnPb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb3Al5O12\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb3Sn13Rh4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb3Tc\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb3Ti3O14\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb3V\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb4Sb2S11.25\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Yb4Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Yb5Au4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Yb6U3O17\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Yb8Ge3Sb5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbAgGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbAgO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YbAl3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbAs\\n\",\n        \"output\": \" 1.02\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbB2Rh3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbB66\\n\",\n        \"output\": \" 1.27\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbBO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbCdHg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbCe2CuS5\\n\",\n        \"output\": \" 1.37\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbCe2CuSe5\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbCuGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbCuSi\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbDyPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YbGa2Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YbGeRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbH2ClO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbIn4Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbIn4Rh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbIr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbMgPd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbMn2O5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbNd2CuS5\\n\",\n        \"output\": \" 1.35\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YbNd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbNdAg2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbPO4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbPmPt2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbPr11Se16\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbPr2CuS5\\n\",\n        \"output\": \" 1.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YbSb\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbSb4Te7\\n\",\n        \"output\": \" 0.22\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbSe\\n\",\n        \"output\": \" 1.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbSi2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"YbSm2CuS5\\n\",\n        \"output\": \" 1.28\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbSmRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbSn2Pd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbSnRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YbSnTe2\\n\",\n        \"output\": \" 0.75\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"YbTe\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbTlS2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbTlSe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"YbWClO4\\n\",\n        \"output\": \" 4.23\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"YbZnAu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"YbZnPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn(Bi19O29)2\\n\",\n        \"output\": \" 2.88\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn(CoO2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn(CuO2)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn(FeN)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn(GaSe2)2\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.01Ga0.99As0.99Se0.01\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.01Ga0.99P0.99S0.01\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.01Ga0.99P0.99Se0.01\\n\",\n        \"output\": \" 2.24\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.01Ga0.99Sb0.99Te0.01\\n\",\n        \"output\": \" 0.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.05Ga0.95Sb0.95Te0.05\\n\",\n        \"output\": \" 0.85\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.15Ga0.85As0.85Se0.15\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.1Ga0.9Sb0.9Te0.1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.25Ga0.75As0.75Se0.25\\n\",\n        \"output\": \" 1.51\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.25Ga0.75P0.75Se0.25\\n\",\n        \"output\": \" 2.18\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn0.2Ga0.8Sb0.8Te0.2\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.2Hg0.8Te1\\n\",\n        \"output\": \" 0.07\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.3Ga0.7P0.7S0.3\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.42Ga0.58As0.58Se0.42\\n\",\n        \"output\": \" 1.67\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.4Hg0.6Se1\\n\",\n        \"output\": \" 0.42\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn0.55Hg0.45Se1\\n\",\n        \"output\": \" 0.8\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.5Ga0.5As0.5Se0.5\\n\",\n        \"output\": \" 1.52\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.5Ga0.5P0.5Se0.5\\n\",\n        \"output\": \" 2.13\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.65Hg0.35Se1\\n\",\n        \"output\": \" 1.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn0.6Ga0.4As0.4Se0.6\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.75Cd0.25Se1\\n\",\n        \"output\": \" 3.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn0.75Hg0.25Se1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.7Ga0.3As0.3Se0.7\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn0.7Ga0.3P0.3Se0.7\\n\",\n        \"output\": \" 2.15\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.85Ga0.15As0.15Se0.85\\n\",\n        \"output\": \" 2.25\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn0.85Hg0.15Se1\\n\",\n        \"output\": \" 1.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn0.86Hg0.14Te1\\n\",\n        \"output\": \" 1.66\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.8Hg0.2Se1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.8Hg0.2Te1\\n\",\n        \"output\": \" 1.4\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.92Hg0.08Te1\\n\",\n        \"output\": \" 1.9\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.94Hg0.06Te1\\n\",\n        \"output\": \" 2.03\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.95Ga0.05P0.05Se0.95\\n\",\n        \"output\": \" 2.4\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.99Ga0.01As0.01Se0.99\\n\",\n        \"output\": \" 2.59\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.99Ga0.01P0.01S0.99\\n\",\n        \"output\": \" 3.7\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.99Ga0.01P0.01Se0.99\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn0.99Ga0.01Sb0.01Te0.99\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.99Hg0.01Se1\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn0.9Ga0.1As0.1Se0.9\\n\",\n        \"output\": \" 2.34\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn0.9Ga0.1P0.1S0.9\\n\",\n        \"output\": \" 2.8\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn0.9Ga0.1P0.1Se0.9\\n\",\n        \"output\": \" 2.3\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn0.9Hg0.1Se1\\n\",\n        \"output\": \" 1.75\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn0.9Hg0.1Te1\\n\",\n        \"output\": \" 1.74\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn2BIr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn2InCuSe4\\n\",\n        \"output\": \" 1.1\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn2InCuTe4\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn2MoSeO7\\n\",\n        \"output\": \" 4.2\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn2Ni9O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn2Sb3O8\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn2SnN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn2TeMoO7\\n\",\n        \"output\": \" 4.1\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn2WN2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn3(BO3)2\\n\",\n        \"output\": \" 2.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn3(PS4)2\\n\",\n        \"output\": \" 3.07\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn3.5Ga1Sn0.5O6\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn3Cd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn3Cu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn3Cu10(TeO6)6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zn3N2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn3P2\\n\",\n        \"output\": \" 1.15\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zn4.5Ga1Sn0.5O7\\n\",\n        \"output\": \" 3.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zn5.5Ga1Sn0.5O8\\n\",\n        \"output\": \" 2.99\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zn6S5Cl2\\n\",\n        \"output\": \" 2.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zn8Ag5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZnAgF5\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZnAs\\n\",\n        \"output\": \" 0.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZnB12(H5O12)2\\n\",\n        \"output\": \" 4.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZnCrO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZnCu2GeS4\\n\",\n        \"output\": \" 2.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZnCu2GeSe4\\n\",\n        \"output\": \" 1.63\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZnCu2SiSe4\\n\",\n        \"output\": \" 2.33\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZnCu2SiTe4\\n\",\n        \"output\": \" 1.47\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZnCu2SnSe4\\n\",\n        \"output\": \" 1.44\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZnCu2SnTe4\\n\",\n        \"output\": \" 1.39\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZnCu3P3O13\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZnGaRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZnHg3(SCl2)2\\n\",\n        \"output\": \" 2.65\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZnHg3(SeCl2)2\\n\",\n        \"output\": \" 2.23\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZnI2\\n\",\n        \"output\": \" 4.53\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZnIrO3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZnSb\\n\",\n        \"output\": \" 1.05\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZnSb2MoO7\\n\",\n        \"output\": \" 3.3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZnSb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZnSi(AgS2)2\\n\",\n        \"output\": \" 3.28\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZnSiAs2\\n\",\n        \"output\": \" 2.12\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZnSiP2\\n\",\n        \"output\": \" 2.07\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZnSn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZnSnO3\\n\",\n        \"output\": \" 3.9\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZnTc\\n\",\n        \"output\": \" 2.37\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZnWO2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr(Fe2Si)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr(Ni2P)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr0.67Ta1.33N3.03O0.12\\n\",\n        \"output\": \" 1.71\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr1.33Ta0.67N1.63O1.89\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr1.33Ta0.67N1.97O1.38\\n\",\n        \"output\": \" 2.31\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr1.33Ta0.67N2.61O0.42\\n\",\n        \"output\": \" 1.93\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr1.86Cu1S4\\n\",\n        \"output\": \" 1.26\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr2(Co7B2)3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zr2Al\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr2Co12P7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr2CuS4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr2HBr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr2In5Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zr2Ni12P7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr2Se\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr2Te\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr3(Al2C3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zr3(Cu2Si3)2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zr3Ag\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr3Al2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zr3Hg\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr3Ir\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zr3NiO\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr3O\\n\",\n        \"output\": \" 0.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr4AlNi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr4Co4Ge7\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr5Al3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr5Al3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr5Sb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr5SiSb3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr5Sn3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zr5Sn4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zr6Al2CoH10\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"Zr6Al2Ni\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"Zr6NiCl15\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr6O\\n\",\n        \"output\": \" 0.18\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"Zr6Sb2Pt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"Zr7P4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"Zr7Sb4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrAl5Ni2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrAlPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrAlRu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZrAlW\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrAu4\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrB2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrC\\n\",\n        \"output\": \" 0.6\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZrCd\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrCrSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrGaPt\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZrGe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrGeRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrHCl\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrHg4(AsCl3)2\\n\",\n        \"output\": \" 2.48\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrHg4(PCl3)2\\n\",\n        \"output\": \" 3.22\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrInCu2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZrInPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrInRh2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrIr2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrMo3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrNiGe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrNiSb\\n\",\n        \"output\": \" 0.55\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZrNiSn\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrO2\\n\",\n        \"output\": \" 4.99\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrPd2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrPd3\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZrRe2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrRh\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZrRu3C\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrS2\\n\",\n        \"output\": \" 2.75\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrSb\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrSbRu\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZrSe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrSe2\\n\",\n        \"output\": \" 2.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrSi2\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its band gap. ->\",\n        \"input\": \"ZrSiTe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Write band gap of given composition. ->\",\n        \"input\": \"ZrTaN3\\n\",\n        \"output\": \" 1.72\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, what is its band gap? ->\",\n        \"input\": \"ZrTe\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrTi2O\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"Tell me band gap of given composition. ->\",\n        \"input\": \"ZrTiF6\\n\",\n        \"output\": \" 0.0\\n\"\n    },\n    {\n        \"instruction\": \"What is band gap of given composition? ->\",\n        \"input\": \"ZrW2\\n\",\n        \"output\": \" 0.0\\n\"\n    }\n]"
  },
  {
    "path": "dataset/matbench_glass/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 17,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('matbench_glass.csv')\\n\",\n    \"slot = {\\\"composition\\\":\\\"composition\\\", \\n\",\n    \"        \\\"glass formation ability\\\":\\\"glass formation ability\\\"}\\n\",\n    \"pair1 = [(\\\"composition\\\", \\\"glass formation ability\\\")]\\n\",\n    \"data_list = []\\n\",\n    \"for df_slice in df.iterrows():\\n\",\n    \"    for p in pair1:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,1)\\n\",\n    \"        ran1 = random.randint(0,1)\\n\",\n    \"        if ran1 == 0:\\n\",\n    \"            form = \\\"glass formation ability\\\"\\n\",\n    \"        elif ran1 == 1:\\n\",\n    \"            form = \\\"glass-forming ability\\\"\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"Does given \\\"+ p[0]+\\\" have \\\"+ form + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Tell me if given \\\"+ p[0]+ \\\" has \\\"+ form + \\\". ->\\\"\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] = \\\" \\\"+str(df_slice[1][slot[p[0]]])+\\\"\\\\n\\\"\\n\",\n    \"        if str(df_slice[1][slot[p[1]]]) == \\\"True\\\":\\n\",\n    \"            answer = \\\" Yes, \\\" + str(df_slice[1][slot[p[0]]]) + \\\" has \\\"+form+\\\".\\\\n\\\"\\n\",\n    \"        else:\\n\",\n    \"            answer = \\\" No, \\\"+ str(df_slice[1][slot[p[0]]]) + \\\" does not have \\\"+form+\\\".\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = answer\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"67848179\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('../2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\\n\",\n    \"print(len(data_list))\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add = int(len(data_list)/30)\\n\",\n    \"print(add)\\n\",\n    \"add_nouns = random.sample(nouns, add)\\n\",\n    \"print(add_nouns[:10])\\n\",\n    \"for an in add_nouns:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran = random.randint(0,1)\\n\",\n    \"    ran1 = random.randint(0,1)\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        form = \\\"glass formation ability\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        form = \\\"glass-forming ability\\\"\\n\",\n    \"    if ran == 0:\\n\",\n    \"        question = \\\"Does given \\\"+ p[0]+\\\" have \\\"+ form + \\\"? ->\\\"\\n\",\n    \"    elif ran == 1:\\n\",\n    \"        question = \\\"Tell me if given \\\"+ p[0]+ \\\" has \\\"+ form + \\\". ->\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] = \\\" \\\"+an+\\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" \\\"+an+\\\" is not a composition and it has no relation with \\\"+form\\\".\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\\n\",\n    \"random.shuffle(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 18,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('matbench_glass.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"ce1a9f8a\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.6.13\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/matbench_glass/matbench_glass.csv",
    "content": "composition,glass formation ability\nAl,FALSE\nAl(NiB)2,TRUE\nAl10Co21B19,TRUE\nAl10Co23B17,TRUE\nAl10Co27B13,TRUE\nAl10Co29B11,FALSE\nAl10Co31B9,FALSE\nAl10Co33B7,FALSE\nAl10Cr3Si7,TRUE\nAl10Fe23B17,TRUE\nAl10Fe27B13,TRUE\nAl10Fe31B9,TRUE\nAl10Fe33B7,TRUE\nAl10Ni23B17,TRUE\nAl10Ni27B13,TRUE\nAl10Ni29B11,TRUE\nAl10Ni31B9,TRUE\nAl10Ni33B7,FALSE\nAl10V3Ge7,FALSE\nAl11(CrSi2)3,TRUE\nAl11(VGe2)3,TRUE\nAl11Cr2Si7,TRUE\nAl11Cr4Si5,FALSE\nAl11Cr5Si4,FALSE\nAl11V2Cu7,TRUE\nAl11V2Ge7,TRUE\nAl11V4Ge5,FALSE\nAl12Co21B17,TRUE\nAl12Co25B13,TRUE\nAl12Co27B11,FALSE\nAl12Cr3Si5,TRUE\nAl12Cr5Si3,FALSE\nAl12CrSi7,FALSE\nAl12Ni25B13,TRUE\nAl12Ni27B11,FALSE\nAl12Ni29B9,FALSE\nAl12Ni31B7,FALSE\nAl12V3Cu5,FALSE\nAl12V3Ge5,TRUE\nAl12VCu7,FALSE\nAl12VGe7,FALSE\nAl13Cr2Si5,TRUE\nAl13Cr3Si4,FALSE\nAl13Cr4Ge3,FALSE\nAl13Cr4Si3,FALSE\nAl13Cr5Si2,FALSE\nAl13Fe3Ni4,FALSE\nAl13Fe4Cu3,TRUE\nAl13Ni6Mo,TRUE\nAl13Si4Ni3,TRUE\nAl13V2Cu5,TRUE\nAl13V2Ge5,TRUE\nAl13V3Cu4,TRUE\nAl13V3Ge4,FALSE\nAl13V4Cu3,FALSE\nAl13VCu6,TRUE\nAl13VGe6,FALSE\nAl14(CrSi)3,FALSE\nAl14(FeNi)3,TRUE\nAl14(Ni7B5)3,FALSE\nAl14(SiNi)3,TRUE\nAl14Cr5Si,FALSE\nAl14CrSi5,FALSE\nAl14Ni25B11,FALSE\nAl14Ni5Mo,TRUE\nAl14VCu5,FALSE\nAl14VGe5,FALSE\nAl15Co2Si3,TRUE\nAl15Cr2Si3,FALSE\nAl15Cr3Si2,FALSE\nAl15Cr4Si,FALSE\nAl15CrSi4,FALSE\nAl15Ni3Mo2,TRUE\nAl15Ni4Mo,TRUE\nAl15V2Cu3,TRUE\nAl15V2Ge3,FALSE\nAl15V3Cu2,FALSE\nAl15VCu4,TRUE\nAl16CrSi3,FALSE\nAl16Ni3Mo,TRUE\nAl16V3Cu,FALSE\nAl16VCu3,TRUE\nAl17Co2Ni,FALSE\nAl17CoNi2,FALSE\nAl17Cr2Si,FALSE\nAl17Cr3,FALSE\nAl17CrSi2,FALSE\nAl17FeNi2,FALSE\nAl17Ni2Mo,TRUE\nAl17V2Cu,TRUE\nAl18CoNi,FALSE\nAl18CrSi,FALSE\nAl18FeCu,TRUE\nAl18FeNi,FALSE\nAl19Cr5Ge26,TRUE\nAl2(Co11B5)3,TRUE\nAl2(Co13B3)3,TRUE\nAl2(Fe13B3)3,TRUE\nAl2(Ni11B5)3,TRUE\nAl2(Ni13B3)3,TRUE\nAl2(Ni9B7)3,TRUE\nAl21(CoNi)2,FALSE\nAl21(FeNi)2,TRUE\nAl21Co5Ge24,TRUE\nAl21Cr4,FALSE\nAl21Fe5Ge24,TRUE\nAl21FeCo3,FALSE\nAl21FeNi3,FALSE\nAl22Co2Ni,FALSE\nAl22Co3,FALSE\nAl22CoNi2,TRUE\nAl22Cr3,FALSE\nAl22Fe2Co,FALSE\nAl22Fe2Ni,FALSE\nAl22Fe3,FALSE\nAl22FeCo2,FALSE\nAl22FeNi2,FALSE\nAl22Ni3,FALSE\nAl23Co2,FALSE\nAl23CoNi,FALSE\nAl23Cr2,FALSE\nAl23Fe2,FALSE\nAl23FeCo,FALSE\nAl23FeNi,FALSE\nAl23Ni2,FALSE\nAl24Co,FALSE\nAl24Cr,FALSE\nAl24Fe,FALSE\nAl24Ni,FALSE\nAl26Cr5Si19,TRUE\nAl26V5Ge19,TRUE\nAl27Mo23,TRUE\nAl29Cr10Si11,FALSE\nAl2Co31B17,TRUE\nAl2Co35B13,TRUE\nAl2Co37B11,TRUE\nAl2Co41B7,FALSE\nAl2Co43B5,FALSE\nAl2Co5B3,TRUE\nAl2Co7B,FALSE\nAl2Cu3,FALSE\nAl2Fe37B11,TRUE\nAl2Fe41B7,TRUE\nAl2Fe43B5,FALSE\nAl2Fe5B3,TRUE\nAl2Ni29B19,TRUE\nAl2Ni31B17,TRUE\nAl2Ni35B13,TRUE\nAl2Ni37B11,TRUE\nAl2Ni5B3,TRUE\nAl2VGe,FALSE\nAl30Cr9Si11,FALSE\nAl32Ni5Ge13,TRUE\nAl33Mo17,TRUE\nAl33Si12Ni5,TRUE\nAl34(Si7Mo15)3,TRUE\nAl34Cr5Si11,TRUE\nAl34V5Ge11,TRUE\nAl35Fe7Cu8,FALSE\nAl35Fe7Ni8,TRUE\nAl35Fe8Ni7,TRUE\nAl36(FeNi)7,TRUE\nAl39Co5Ge6,TRUE\nAl39Fe5Ge6,TRUE\nAl3CrSi,FALSE\nAl3Cu,FALSE\nAl3Cu2,FALSE\nAl3Fe80P17,TRUE\nAl3VGe,FALSE\nAl41Fe2Ni7,FALSE\nAl42Fe3Ni5,FALSE\nAl42Fe7Si,FALSE\nAl42FeCo7,FALSE\nAl42FeNi7,FALSE\nAl43Co7,FALSE\nAl43CoNi6,FALSE\nAl43Cr7,FALSE\nAl43Fe2Co5,FALSE\nAl43Fe2Ni5,FALSE\nAl43Fe3Co4,FALSE\nAl43Fe3Ni4,FALSE\nAl43Fe4Co3,FALSE\nAl43Fe4Ni3,FALSE\nAl43Fe5Co2,FALSE\nAl43Fe5Ni2,FALSE\nAl43Fe6Ni,FALSE\nAl43Fe6Si,FALSE\nAl43FeCo6,TRUE\nAl43FeNi6,TRUE\nAl43Ni7,FALSE\nAl44(CoNi)3,FALSE\nAl44(FeCo)3,FALSE\nAl44(FeNi)3,FALSE\nAl44Co5Ni,FALSE\nAl44CoNi5,FALSE\nAl44Cr5Si,FALSE\nAl44Fe5Co,FALSE\nAl44Fe5Ni,FALSE\nAl44Fe5Si,FALSE\nAl44FeCo5,FALSE\nAl44FeNi5,FALSE\nAl45Co2Ni3,FALSE\nAl45Co3Ni2,FALSE\nAl45Co4Ni,FALSE\nAl45CoNi4,FALSE\nAl45Fe2Co3,FALSE\nAl45Fe2Ni3,FALSE\nAl45Fe3Co2,FALSE\nAl45Fe3Ni2,FALSE\nAl45Fe4Co,FALSE\nAl45Fe4Ni,FALSE\nAl45Fe4Si,FALSE\nAl45FeCo4,FALSE\nAl45FeNi4,FALSE\nAl46Co3Ni,FALSE\nAl46CoNi3,FALSE\nAl46Fe3Co,FALSE\nAl46Fe3Ni,FALSE\nAl46FeCo3,FALSE\nAl46FeNi3,FALSE\nAl47Co2Ni,FALSE\nAl47Co3,FALSE\nAl47CoNi2,FALSE\nAl47Cr3,FALSE\nAl47Fe2Co,FALSE\nAl47Fe2Ni,FALSE\nAl47Fe3,FALSE\nAl47FeCo2,FALSE\nAl47FeNi2,FALSE\nAl47Ni3,FALSE\nAl48CoNi,FALSE\nAl48FeCo,FALSE\nAl48FeNi,FALSE\nAl49Co,FALSE\nAl49Co10Si41,TRUE\nAl49Fe,FALSE\nAl49Ni,FALSE\nAl4Co29B17,TRUE\nAl4Co31B15,TRUE\nAl4Co33B13,TRUE\nAl4Co35B11,TRUE\nAl4Co37B9,TRUE\nAl4Co39B7,FALSE\nAl4Co41B5,FALSE\nAl4Cr,FALSE\nAl4Cu,FALSE\nAl4Fe35B11,TRUE\nAl4Fe37B9,TRUE\nAl4Fe39B7,TRUE\nAl4Fe41B5,FALSE\nAl4Ni,FALSE\nAl4Ni25B21,TRUE\nAl4Ni27B19,TRUE\nAl4Ni29B17,TRUE\nAl4Ni31B15,TRUE\nAl4Ni33B13,TRUE\nAl4Ni35B11,TRUE\nAl4Ni37B9,TRUE\nAl52Co23Si25,TRUE\nAl52Fe23Ge25,TRUE\nAl52Fe23Si25,TRUE\nAl52Si25Ni23,TRUE\nAl53Si16Mo31,TRUE\nAl57Co18Ge25,TRUE\nAl57Cr23Si20,FALSE\nAl57Cr28Si15,FALSE\nAl57Fe27Ni16,FALSE\nAl57V18Ge25,TRUE\nAl58Cr17Si25,TRUE\nAl59Cr19Si22,FALSE\nAl59Ni10Ge31,TRUE\nAl5Fe2Cu3,FALSE\nAl5V2Ge3,FALSE\nAl5VCu4,FALSE\nAl5VGe4,FALSE\nAl6(Co3B)11,TRUE\nAl6(Fe3B)11,TRUE\nAl6(Ni3B)11,TRUE\nAl61(Cr7Si6)3,FALSE\nAl61Cr10Ge29,TRUE\nAl62(CrSi)19,FALSE\nAl62.5Fe12.5Cu25,FALSE\nAl62Fe17Cu21,FALSE\nAl62Ni13Ge25,TRUE\nAl63Cr15Si22,FALSE\nAl63Cr19Si18,FALSE\nAl63Fe12Si25,TRUE\nAl63Si6Mo31,TRUE\nAl64Fe13Cu23,FALSE\nAl65(Fe3Ni2)7,FALSE\nAl65Si17.5Ni17.5,TRUE\nAl65Si19Ni16,TRUE\nAl66.5Si18.5Ni15,TRUE\nAl67(Fe7Ni4)3,FALSE\nAl67.5Si17.5Ni15,TRUE\nAl67V13Cu20,TRUE\nAl68Cr15Si17,FALSE\nAl69Co6Ge25,TRUE\nAl69Fe13Cu18,FALSE\nAl69Fe6Ge25,TRUE\nAl69Ni6Ge25,TRUE\nAl69V6Ge25,TRUE\nAl6Co25B19,TRUE\nAl6Co27B17,TRUE\nAl6Co29B15,TRUE\nAl6Co31B13,TRUE\nAl6Co35B9,TRUE\nAl6Co37B7,FALSE\nAl6Co39B5,FALSE\nAl6Co41B3,FALSE\nAl6Co9B10,TRUE\nAl6Cr3Si,FALSE\nAl6CrGe3,TRUE\nAl6CrSi3,TRUE\nAl6Fe37B7,TRUE\nAl6Fe39B5,FALSE\nAl6Fe41B3,FALSE\nAl6Ni27B17,TRUE\nAl6Ni29B15,TRUE\nAl6Ni31B13,TRUE\nAl6Ni35B9,TRUE\nAl6Ni37B7,FALSE\nAl6NiGe3,TRUE\nAl6VCu3,TRUE\nAl6VGe3,TRUE\nAl70Si17Ni13,TRUE\nAl71Co4Si25,TRUE\nAl71Cr4Si25,TRUE\nAl71Fe15Cu14,TRUE\nAl71Si25Ni4,TRUE\nAl72Fe13Ni15,FALSE\nAl73Fe13Cu14,FALSE\nAl75Fe14Ni11,TRUE\nAl77V3Cu20,FALSE\nAl78Fe7Cu15,FALSE\nAl79(FeNi2)7,TRUE\nAl79Si11Ni10,TRUE\nAl7Cr2Si,FALSE\nAl7CrSi2,FALSE\nAl7Cu3,FALSE\nAl7Fe2Ni,TRUE\nAl7Ni18,FALSE\nAl7Ni2Mo,TRUE\nAl7Ni3,FALSE\nAl7VCu2,TRUE\nAl7VGe2,FALSE\nAl8(Co11B3)3,TRUE\nAl8(Co5B)7,TRUE\nAl8(Co9B5)3,TRUE\nAl8(Fe11B3)3,TRUE\nAl8(Fe5B)7,TRUE\nAl8(Ni11B3)3,TRUE\nAl8(Ni5B)7,FALSE\nAl8(Ni9B5)3,TRUE\nAl81Cr19,FALSE\nAl82(Fe5Ni)3,TRUE\nAl83Cr17,FALSE\nAl83Fe3Ni14,FALSE\nAl84Fe3Ni13,FALSE\nAl85(FeNi4)3,FALSE\nAl85(Ni4Mo)3,TRUE\nAl85CoNi14,FALSE\nAl85Fe2Ni13,FALSE\nAl85Fe8Si7,FALSE\nAl85FeNi14,FALSE\nAl86(FeNi)7,FALSE\nAl86.7Fe1Ni12.3,TRUE\nAl86Co3Ni11,FALSE\nAl86Co5Ni9,FALSE\nAl86CoNi13,FALSE\nAl86Fe3Ni11,TRUE\nAl86Fe5Ni9,FALSE\nAl86FeNi13,FALSE\nAl87.5Fe0.5Ni12,TRUE\nAl87.5Fe2Ni10.5,TRUE\nAl87.5Fe3.5Ni9,TRUE\nAl87Co2Ni11,TRUE\nAl87Co3Ni10,FALSE\nAl87Co4Ni9,FALSE\nAl87Co5Ni8,FALSE\nAl87CoNi12,TRUE\nAl87Fe2Co11,TRUE\nAl87Fe2Ni11,TRUE\nAl87Fe3Ni10,TRUE\nAl87Fe4Co9,FALSE\nAl87Fe4Ni9,FALSE\nAl87Fe5Ni8,FALSE\nAl87Fe6Ni7,FALSE\nAl87FeNi12,TRUE\nAl87V5Cu8,FALSE\nAl87V8Cu5,FALSE\nAl88(Co3Ni)3,FALSE\nAl88(CoNi3)3,FALSE\nAl88(FeNi3)3,TRUE\nAl88.5Fe3Ni8.5,TRUE\nAl88Co11Ni,FALSE\nAl88Co5Ni7,TRUE\nAl88Co7Ni5,FALSE\nAl88CoNi11,FALSE\nAl88Fe5Ni7,FALSE\nAl88FeNi11,TRUE\nAl89Co2Ni9,FALSE\nAl89Co3Ni8,FALSE\nAl89Co4Ni7,FALSE\nAl89Co5Ni6,FALSE\nAl89Co6Ni5,FALSE\nAl89CoNi10,FALSE\nAl89Fe2Ni9,FALSE\nAl89Fe3Ni8,FALSE\nAl89Fe4Ni7,FALSE\nAl89Fe5Ni6,FALSE\nAl89Fe6Ni5,FALSE\nAl89Fe7Ni4,FALSE\nAl89Fe9Ni2,FALSE\nAl89FeNi10,FALSE\nAl8Co25B17,TRUE\nAl8Co29B13,TRUE\nAl8Co31B11,TRUE\nAl8Co37B5,FALSE\nAl8CrSi,FALSE\nAl8Fe29B13,TRUE\nAl8Fe31B11,TRUE\nAl8Fe37B5,FALSE\nAl8Ni23B19,TRUE\nAl8Ni25B17,TRUE\nAl8Ni29B13,TRUE\nAl8Ni31B11,TRUE\nAl8VCu,TRUE\nAl90FeNi9,FALSE\nAl91(Fe2Ni)3,FALSE\nAl91(FeNi2)3,FALSE\nAl91Co2Ni7,FALSE\nAl91CoNi8,FALSE\nAl91Fe2Ni7,FALSE\nAl91FeNi8,FALSE\nAl92Fe5Ni3,FALSE\nAl9Co,FALSE\nAl9Cr,FALSE\nAl9Cr3Si8,FALSE\nAl9Cr4Si7,FALSE\nAl9Fe,FALSE\nAl9Ni,FALSE\nAl9V3Ge8,FALSE\nAlCu,FALSE\nAlFe17Si2,TRUE\nB12Mo23Ru15,TRUE\nB15(Mo3Ru2)17,TRUE\nB3Mo17,FALSE\nB3Mo7,FALSE\nB5(Mo3Rh7)2,TRUE\nB8Mo55.5Ru36.5,TRUE\nBMo3,FALSE\nBMo4,FALSE\nBMo8P,TRUE\nBMo9,FALSE\nBa10La53.5Cu36.5,TRUE\nBa10La56.5Cu33.5,TRUE\nBa2(La9Cu7)3,TRUE\nBa2La11Cu7,TRUE\nBa2La13Cu10,TRUE\nBa2La59Cu39,TRUE\nBa2La71Cu27,TRUE\nBa3La56Cu41,TRUE\nBa3La57Cu40,TRUE\nBa4(La23Cu9)3,TRUE\nBa4.5La68Cu27.5,TRUE\nBa4La31Cu15,TRUE\nBa5La29Cu16,TRUE\nBa5La53Cu42,TRUE\nBa67La28Cu5,TRUE\nBa7.5La63.5Cu29,TRUE\nBa7La51.5Cu41.5,TRUE\nBa7La65Cu28,TRUE\nBa9(La4Cu3)13,TRUE\nBa9.5La52.5Cu38,TRUE\nBa9La60Cu31,TRUE\nBaLa61Cu38,TRUE\nBe2Fe7B,TRUE\nCa(La5Cu2)7,TRUE\nCa1.25Al88.75Ni10,FALSE\nCa1.5La71Cu27.5,TRUE\nCa10Al87.5Fe2.5,FALSE\nCa10Al87.5Ni2.5,FALSE\nCa11Al89,TRUE\nCa11Mg89,FALSE\nCa12Mg7Ga,TRUE\nCa14(MgAl)3,TRUE\nCa15Mg3Cu2,TRUE\nCa1La61.5Cu37.5,TRUE\nCa1La71.5Cu27.5,TRUE\nCa2.5Al87.5Ni10,FALSE\nCa2.5Al92.5Fe5,FALSE\nCa2.5Al92.5Ni5,FALSE\nCa2Al17Co,TRUE\nCa2Al17Cu,TRUE\nCa2Al17Fe,TRUE\nCa2Al17Ni,TRUE\nCa2Al17Zn,TRUE\nCa2La60.5Cu37.5,TRUE\nCa2Mg17Zn,TRUE\nCa2MgAl17,TRUE\nCa3Al2,TRUE\nCa3AlGa,TRUE\nCa3La59.5Cu37.5,TRUE\nCa3La68.5Cu28.5,TRUE\nCa3Mg2,TRUE\nCa3MgGa,TRUE\nCa4La58.5Cu37.5,TRUE\nCa4La67Cu29,TRUE\nCa5(Mg3Cu2)3,TRUE\nCa5La57.5Cu37.5,TRUE\nCa5Mg3Cu2,TRUE\nCa6.5La56.5Cu37,TRUE\nCa6Al3Ga,TRUE\nCa6AlGa3,TRUE\nCa6La63Cu31,TRUE\nCa6Mg3Ga,TRUE\nCa6MgGa3,TRUE\nCa7.5Al87.5Fe5,TRUE\nCa7.5Al87.5Ni5,TRUE\nCa7.5Al90Fe2.5,TRUE\nCa7.5Al90Ni2.5,TRUE\nCa7.5Al92.5,FALSE\nCa7.5La56.5Cu36,TRUE\nCa7.5Mg82.5Cu10,TRUE\nCa7.5Mg82.5Zn10,FALSE\nCa7.5Mg87.5Cu5,TRUE\nCa7.5Mg87.5Zn5,FALSE\nCa7.5Mg92.5,FALSE\nCa70Mg7.5Al22.5,TRUE\nCa7Al3,TRUE\nCa7Cu3,TRUE\nCa7La61Cu32,TRUE\nCa7Mg2Cu,TRUE\nCa7Mg3,TRUE\nCa7MgCu2,TRUE\nCa8.5La56.5Cu35,TRUE\nCa8.5La58.5Cu33,TRUE\nCa8La59.5Cu32.5,TRUE\nCa9Al91,TRUE\nCa9La57.5Cu33.5,TRUE\nCaAl17Ni2,FALSE\nCaAl18Fe,FALSE\nCaAl18Ni,FALSE\nCaAl8Ni,FALSE\nCaAl9,TRUE\nCaLa13Cu6,TRUE\nCaMg17Cu2,FALSE\nCaMg17Zn2,FALSE\nCaMg18Cu,FALSE\nCaMg18Zn,FALSE\nCaMg7Al2,TRUE\nCaMg8Zn,TRUE\nCaMg9,FALSE\nCe(Al2Ni)3,TRUE\nCe(Al6Fe)7,FALSE\nCe(Cu2Ag)3,TRUE\nCe(Cu7Ag5)2,TRUE\nCe(CuAg2)3,FALSE\nCe(Mg2Ni)3,TRUE\nCe(MgNi)2,FALSE\nCe10(Al29Cr)3,TRUE\nCe10Al61Ni29,TRUE\nCe10Al77Co13,FALSE\nCe10Al83Cr7,FALSE\nCe10Al89Ni,TRUE\nCe10Mn7Al83,FALSE\nCe10Nb13Al77,FALSE\nCe11Al5Ni4,TRUE\nCe11Al89,TRUE\nCe13Al85V2,FALSE\nCe13Al87,TRUE\nCe17Al71Fe12,FALSE\nCe18Al67Fe15,FALSE\nCe18Al77Fe5,FALSE\nCe2(Al5Co)3,FALSE\nCe2(Al5Cu)3,TRUE\nCe2(Al5Fe)3,FALSE\nCe2(Al5Ni)3,TRUE\nCe2(AlCu15)3,FALSE\nCe2(Mg5Cu)3,TRUE\nCe2(Mg5Ni)3,TRUE\nCe23Al60Fe17,FALSE\nCe23Al64Fe13,FALSE\nCe25.5Al62.5Fe12,FALSE\nCe25Al62.5Fe12.5,FALSE\nCe2Al17Co,TRUE\nCe2Al17Cr,TRUE\nCe2Al17Cu,TRUE\nCe2Al17Fe,TRUE\nCe2Al17Ni,TRUE\nCe2Al17V,FALSE\nCe2Al22V,FALSE\nCe2Al23,TRUE\nCe2Al2Cu21,TRUE\nCe2Al3Cu20,TRUE\nCe2Al43Ni5,TRUE\nCe2Al47Co,FALSE\nCe2Al47Fe,FALSE\nCe2Al5Cu43,FALSE\nCe2Al7Fe,FALSE\nCe2Al7Ni,FALSE\nCe2Al83Cu15,FALSE\nCe2Al93Cr5,FALSE\nCe2Al95Co3,FALSE\nCe2AlCu22,FALSE\nCe2Cu13Ag10,TRUE\nCe2Cu23Ag25,TRUE\nCe2Cu53Ag45,FALSE\nCe2Mg13Cu5,TRUE\nCe2Mg17Cu,FALSE\nCe2Mg17Ni,TRUE\nCe2Mg5Ni3,TRUE\nCe2Mg7Cu,FALSE\nCe2Mg7Ni,FALSE\nCe2Mn5Al93,FALSE\nCe2MnAl17,TRUE\nCe2NbAl17,TRUE\nCe3Al13Fe4,FALSE\nCe3Al13Ni4,TRUE\nCe3Al14Cu3,FALSE\nCe3Al14Fe3,FALSE\nCe3Al14Ni3,TRUE\nCe3Al15Co2,FALSE\nCe3Al15Cu2,FALSE\nCe3Al15Fe2,FALSE\nCe3Al16Co,FALSE\nCe3Al16Cr,FALSE\nCe3Al16Cu,FALSE\nCe3Al16Fe,FALSE\nCe3Al16Ni,FALSE\nCe3Al22,TRUE\nCe3Al3Cu44,FALSE\nCe3Al42Ni5,TRUE\nCe3Al43Ni4,TRUE\nCe3Al47,FALSE\nCe3Al4Cu43,FALSE\nCe3Al5Cu42,FALSE\nCe3Al6Cu41,FALSE\nCe3Al7Cu40,FALSE\nCe3Al90Co7,TRUE\nCe3Al90Fe7,TRUE\nCe3AlCu46,FALSE\nCe3Cu32Ag15,TRUE\nCe3Cu37Ag10,TRUE\nCe3Cu37Ag60,FALSE\nCe3Cu42Ag5,TRUE\nCe3Cu47Ag50,TRUE\nCe3Cu52Ag45,TRUE\nCe3Cu57Ag40,TRUE\nCe3Cu62Ag35,FALSE\nCe3Cu67Ag30,FALSE\nCe3Cu77Ag20,FALSE\nCe3Cu87Ag10,FALSE\nCe3Mg12Cu5,FALSE\nCe3Mg13Cu4,TRUE\nCe3Mg14Cu3,TRUE\nCe3Mg15Cu2,FALSE\nCe3Mg15Ni2,TRUE\nCe3Mg16Cu,FALSE\nCe3Mg4Ni3,FALSE\nCe3Mg85Zn12,TRUE\nCe3Nb2Al15,FALSE\nCe3NbAl16,FALSE\nCe3NbAl46,TRUE\nCe4(Cu17Ag15)3,TRUE\nCe4(Cu27Ag5)3,FALSE\nCe4Al13Fe3,FALSE\nCe4Al15Fe,FALSE\nCe4Al3Cu43,FALSE\nCe4Al41Ni5,TRUE\nCe4Al5Cu41,TRUE\nCe4Al7Cu39,FALSE\nCe4AlCu45,FALSE\nCe4Cu43Ag3,FALSE\nCe4Cu61Ag35,TRUE\nCe4Mg11Cu5,FALSE\nCe4Mg13Cu3,FALSE\nCe4Mg15Cu,FALSE\nCe4NbAl45,TRUE\nCe5(Al2Cu13)3,FALSE\nCe5(Al4Fe)3,FALSE\nCe5(AlCu14)3,TRUE\nCe5(Mg4Ni)9,TRUE\nCe5Al13Fe2,FALSE\nCe5Al2Cu43,FALSE\nCe5Al44Co,TRUE\nCe5Al44Cu,TRUE\nCe5Al44Fe,TRUE\nCe5Al44V,TRUE\nCe5Al4Cu41,TRUE\nCe5Al7Cu38,FALSE\nCe5Al83Co12,TRUE\nCe5Al87Ni8,TRUE\nCe5Al88Cu7,FALSE\nCe5Al91Ni4,TRUE\nCe5AlCu44,FALSE\nCe5Mn2Al43,TRUE\nCe5MnAl44,TRUE\nCe5NbAl44,TRUE\nCe6Al85Ni9,TRUE\nCe6Al87Ni7,TRUE\nCe6Al89V5,FALSE\nCe6Cu39Ag55,TRUE\nCe6Cu59Ag35,TRUE\nCe6Cu69Ag25,TRUE\nCe6Cu79Ag15,TRUE\nCe6Cu89Ag5,FALSE\nCe6Mn5Al89,FALSE\nCe7Al83Cu10,TRUE\nCe7Al83Fe10,TRUE\nCe7Al93,TRUE\nCe7Nb10Al83,TRUE\nCe8Al87Co5,TRUE\nCe8Al87Cr5,FALSE\nCe8Al87Cu5,TRUE\nCe8Al87Fe5,TRUE\nCe8Al89Cr3,FALSE\nCe8Cu37Ag55,TRUE\nCe8Cu87Ag5,FALSE\nCe8Mn5Al87,FALSE\nCe8Nb5Al87,TRUE\nCe9Al91,TRUE\nCeAl13Ni6,TRUE\nCeAl15Co4,FALSE\nCeAl15Cu4,FALSE\nCeAl15Ni4,TRUE\nCeAl16Co3,TRUE\nCeAl16Cu3,TRUE\nCeAl16Ni3,TRUE\nCeAl17Co2,TRUE\nCeAl17Cu2,TRUE\nCeAl17Fe2,TRUE\nCeAl17Ni2,TRUE\nCeAl18Co,TRUE\nCeAl18Cu,FALSE\nCeAl18Fe,TRUE\nCeAl18Ni,FALSE\nCeAl19,FALSE\nCeAl3Fe,FALSE\nCeAl3Ni,FALSE\nCeAl44Co5,TRUE\nCeAl44Cu5,FALSE\nCeAl44Fe5,TRUE\nCeAl44Ni5,TRUE\nCeAl47Cr2,FALSE\nCeAl47Fe2,FALSE\nCeAl47V2,FALSE\nCeAl5Cu44,FALSE\nCeAl7Cu2,FALSE\nCeAl7Fe2,FALSE\nCeAl7Ni2,TRUE\nCeAl89Fe10,FALSE\nCeAl8Co,TRUE\nCeAl8Cr,FALSE\nCeAl8Cu,TRUE\nCeAl8Fe,TRUE\nCeAl8Ni,TRUE\nCeAl8V,FALSE\nCeAl9,TRUE\nCeAlCu23,FALSE\nCeAlCu8,FALSE\nCeCu10Ag9,TRUE\nCeCu11Ag8,TRUE\nCeCu12Ag7,TRUE\nCeCu13Ag6,FALSE\nCeCu15Ag4,FALSE\nCeCu17Ag2,FALSE\nCeCu18Ag,FALSE\nCeCu19Ag5,FALSE\nCeCu24Ag25,FALSE\nCeCu29Ag20,FALSE\nCeCu2Ag7,FALSE\nCeCu4Ag5,TRUE\nCeCu59Ag40,FALSE\nCeCu5Ag14,FALSE\nCeCu5Ag4,TRUE\nCeCu7Ag12,FALSE\nCeCu7Ag2,TRUE\nCeCu8Ag,TRUE\nCeCu8Ag11,TRUE\nCeCu9Ag10,TRUE\nCeMg13Cu6,TRUE\nCeMg14Cu5,TRUE\nCeMg15Cu4,TRUE\nCeMg15Ni4,TRUE\nCeMg16Cu3,TRUE\nCeMg17Cu2,TRUE\nCeMg17Ni2,TRUE\nCeMg18Cu,FALSE\nCeMg18Ni,FALSE\nCeMg2Cu,FALSE\nCeMg3Cu,FALSE\nCeMg3Ni,TRUE\nCeMg7Cu2,TRUE\nCeMg7Ni2,TRUE\nCeMg8Cu,TRUE\nCeMg8Ni,TRUE\nCeMg9,FALSE\nCeMn2Al17,FALSE\nCeMn2Al47,FALSE\nCeMn5Al44,FALSE\nCeMnAl8,FALSE\nCeNb2Al17,FALSE\nCeNbAl18,FALSE\nCeNbAl8,TRUE\nCo,FALSE\nCo1.7Si16.5Pd81.8,TRUE\nCo10Ni68.5P21.5,FALSE\nCo10Ni71P19,FALSE\nCo10Ni73P17,FALSE\nCo10Si16.5Pd73.5,TRUE\nCo11Mo9C5,TRUE\nCo12.5Ni66P21.5,FALSE\nCo12.5Ni68.5P19,FALSE\nCo12.5Ni70.5P17,FALSE\nCo12.5Si16.5Pd71,TRUE\nCo12B8C5,FALSE\nCo12B9C4,FALSE\nCo12Mo8C5,TRUE\nCo12Mo9C4,TRUE\nCo13(B2C)4,TRUE\nCo13(B3C)3,FALSE\nCo13B7,TRUE\nCo13B7C5,FALSE\nCo13Mo7C5,TRUE\nCo13Si2B5,TRUE\nCo13Si3B4,TRUE\nCo13Si4B3,FALSE\nCo13SiB6,TRUE\nCo13W3C4,FALSE\nCo13W4C3,FALSE\nCo14(SiB)3,TRUE\nCo14(WC)3,TRUE\nCo14B6C5,TRUE\nCo14B7C4,TRUE\nCo14B8C3,TRUE\nCo14B9C2,FALSE\nCo14Mo6C5,TRUE\nCo14Mo7C4,TRUE\nCo14Ni64.5P21.5,FALSE\nCo14Ni67P19,FALSE\nCo14Ni69P17,FALSE\nCo14Si5C,FALSE\nCo14SiB5,TRUE\nCo15(B3C2)2,TRUE\nCo15(B4C)2,TRUE\nCo15(Mo3C2)2,TRUE\nCo15B7C3,TRUE\nCo15B9C,TRUE\nCo15Si16.5Pd68.5,TRUE\nCo15Si2B3,TRUE\nCo15Si2C3,FALSE\nCo15Si3B2,TRUE\nCo15Si3C2,FALSE\nCo15Si4B,FALSE\nCo15Si4C,FALSE\nCo15SiB4,TRUE\nCo15SiC4,FALSE\nCo15W2C3,FALSE\nCo15W3C2,FALSE\nCo15WC4,FALSE\nCo16(B2C)3,TRUE\nCo16B4C5,FALSE\nCo16B5C4,TRUE\nCo16B7C2,TRUE\nCo16B8C,TRUE\nCo16B9,TRUE\nCo16Mo4C5,TRUE\nCo16Mo5C4,TRUE\nCo16Ni65P19,FALSE\nCo16Si3C,FALSE\nCo16SiB3,TRUE\nCo16SiC3,FALSE\nCo16W3C,FALSE\nCo16W5C4,FALSE\nCo16WC3,FALSE\nCo17(B3C)2,TRUE\nCo17(BC)4,FALSE\nCo17(MoC)4,TRUE\nCo17(SiB)4,TRUE\nCo17(WC)4,FALSE\nCo17B3,FALSE\nCo17B5C3,TRUE\nCo17B7C,TRUE\nCo17B8,TRUE\nCo17C3,FALSE\nCo17Mo3C5,TRUE\nCo17Si3,FALSE\nCo17SiB2,FALSE\nCo17SiC2,FALSE\nCo17W2C,FALSE\nCo17W3C5,FALSE\nCo17W5C3,FALSE\nCo18B3C4,FALSE\nCo18B4C3,TRUE\nCo18B5C2,TRUE\nCo18B6C,TRUE\nCo18B7,TRUE\nCo18Mo3C4,TRUE\nCo18W3C4,TRUE\nCo18WC,FALSE\nCo19(B2C)2,TRUE\nCo19(BC)3,TRUE\nCo19B5C,TRUE\nCo19B6,TRUE\nCo19Si,FALSE\nCo2(Ni11P3)7,TRUE\nCo20.9Si16.5Pd62.6,FALSE\nCo20B2C3,FALSE\nCo20B3C2,FALSE\nCo20B4C,TRUE\nCo21(BC)2,FALSE\nCo21B3C,FALSE\nCo21B4,TRUE\nCo21Mo20C9,FALSE\nCo22B2C,FALSE\nCo22B3,TRUE\nCo23(Mo2C)9,TRUE\nCo23Mo16C11,TRUE\nCo23Mo20C7,FALSE\nCo25Mo14C11,TRUE\nCo25Mo16C9,TRUE\nCo25Mo18C7,FALSE\nCo27Mo12C11,TRUE\nCo27Mo14C9,TRUE\nCo29(Mo4C3)3,TRUE\nCo29(W4C3)3,FALSE\nCo29B20C,FALSE\nCo29Mo10C11,TRUE\nCo2Ni78.5P19.5,TRUE\nCo2Ni81P17,FALSE\nCo3.5Ni74.5P22,FALSE\nCo3.5Ni75.5P21,TRUE\nCo3.5Ni77P19.5,TRUE\nCo3.5Ni78.5P18,TRUE\nCo3.5Ni79.5P17,FALSE\nCo31B18C,TRUE\nCo31B19,TRUE\nCo31Mo10C9,TRUE\nCo31Mo12C7,FALSE\nCo31Mo8C11,TRUE\nCo31W10C9,FALSE\nCo33B16C,TRUE\nCo33B17,TRUE\nCo33Mo8C9,TRUE\nCo33Ni33B34,TRUE\nCo33W10C7,FALSE\nCo33W8C9,FALSE\nCo34Mo5C11,TRUE\nCo34W7C9,FALSE\nCo35(Mo2C3)3,TRUE\nCo35(W2C3)3,TRUE\nCo35Mo8C7,FALSE\nCo35W7C8,TRUE\nCo35W8C7,TRUE\nCo36(WC)7,TRUE\nCo36Mo5C9,TRUE\nCo36W5C9,FALSE\nCo37B13,TRUE\nCo37Mo4C9,FALSE\nCo37Mo5C8,FALSE\nCo37Mo6C7,FALSE\nCo37W5C8,FALSE\nCo37W7C6,FALSE\nCo38Mo5C7,FALSE\nCo38W5C7,FALSE\nCo39B11,TRUE\nCo39Si5B6,TRUE\nCo3B,TRUE\nCo3B2,TRUE\nCo3BC,TRUE\nCo3MoC,TRUE\nCo3Si,FALSE\nCo3SiB,FALSE\nCo3WC,FALSE\nCo4.2Si16.5Pd79.3,TRUE\nCo40Si3B7,TRUE\nCo41B9,TRUE\nCo41Si2B7,FALSE\nCo41Si4B5,FALSE\nCo4B,TRUE\nCo4C,FALSE\nCo4Si,FALSE\nCo59B41,TRUE\nCo5Ni73P22,FALSE\nCo5Ni74P21,TRUE\nCo5Ni75.5P19.5,TRUE\nCo5Ni77P18,TRUE\nCo5Ni78P17,FALSE\nCo6.7Si16.5Pd76.8,TRUE\nCo60Si17.5B22.5,FALSE\nCo62.5Si12.5B25,TRUE\nCo62.5Si17.5B20,FALSE\nCo65Si22.5C12.5,TRUE\nCo65Si7.5B27.5,TRUE\nCo65W17.5C17.5,FALSE\nCo67.5Si12.5B20,TRUE\nCo67.5Si15C17.5,TRUE\nCo67.5Si17.5C15,TRUE\nCo67.5Si20C12.5,TRUE\nCo67.5Si22.5C10,TRUE\nCo67.5Si7.5B25,TRUE\nCo67.5W17.5C15,FALSE\nCo67.5W20C12.5,FALSE\nCo7(Ni24P7)3,TRUE\nCo7(Ni25P6)3,TRUE\nCo70.5Si14.75B14.75,TRUE\nCo70W17.5C12.5,FALSE\nCo71B29,TRUE\nCo72.5Si12.5B15,TRUE\nCo72.5Si7.5B20,TRUE\nCo72.5W15C12.5,TRUE\nCo73Si13.5B13.5,TRUE\nCo74.5W7.5C18,FALSE\nCo75Si12.5B12.5,TRUE\nCo75Si7.5B17.5,TRUE\nCo75W12.5C12.5,FALSE\nCo77.5Si10B12.5,TRUE\nCo77.5Si12.5B10,TRUE\nCo77.5Si15B7.5,TRUE\nCo77.5Si7.5B15,TRUE\nCo77.5W10C12.5,FALSE\nCo77.5W15C7.5,FALSE\nCo77.5W7.5C15,FALSE\nCo77W5C18,FALSE\nCo78(SiB)11,TRUE\nCo7B3,TRUE\nCo7MoC2,TRUE\nCo7Ni71P22,FALSE\nCo7Ni73.5P19.5,TRUE\nCo7Ni76P17,FALSE\nCo7Si2B,FALSE\nCo7Si3,FALSE\nCo7SiB2,TRUE\nCo7SiC2,FALSE\nCo7W2C,FALSE\nCo7WC2,FALSE\nCo80.5Si7B12.5,FALSE\nCo80B7P13,TRUE\nCo80Si7.5B12.5,TRUE\nCo80W7.5C12.5,FALSE\nCo81.5B18.5,TRUE\nCo82.5W10C7.5,FALSE\nCo82.5W7.5C10,FALSE\nCo83B17,TRUE\nCo85W2.5C12.5,FALSE\nCo85W7.5C7.5,FALSE\nCo87.5W2.5C10,FALSE\nCo89B11,TRUE\nCo8SiB,FALSE\nCo8WC,FALSE\nCo95W2.5C2.5,FALSE\nCo9C,FALSE\nCo9Ni69.5P21.5,FALSE\nCo9Ni72P19,TRUE\nCo9Ni74P17,FALSE\nCo9Si,FALSE\nCoNi38P11,FALSE\nCoNi40P9,TRUE\nCoSi2Pd7,TRUE\nCr(Ge2Pd9)9,TRUE\nCr0.5Si20Pd79.5,TRUE\nCr10Co11C4,FALSE\nCr10Fe13C2,FALSE\nCr10Fe31B9,TRUE\nCr10Fe33B7,TRUE\nCr10Fe37B3,FALSE\nCr10Fe39B,FALSE\nCr10Ni4Mo11,TRUE\nCr10Ni71P19,TRUE\nCr11(Co10C3)3,FALSE\nCr11(Fe11B2)3,TRUE\nCr11(Fe12B)3,FALSE\nCr11Co9C5,TRUE\nCr11Fe29C10,FALSE\nCr11Fe34B5,FALSE\nCr11Fe35B4,FALSE\nCr11Fe74B15,TRUE\nCr12Co9C4,TRUE\nCr12Fe31B7,TRUE\nCr12Fe33B5,TRUE\nCr12Fe35B3,FALSE\nCr12Fe73B15,TRUE\nCr13(Ni3Mo)3,TRUE\nCr13Co26C11,FALSE\nCr13Co28C9,TRUE\nCr13Fe28C9,TRUE\nCr13Fe30B7,TRUE\nCr13Fe31B6,TRUE\nCr13Fe32B5,TRUE\nCr13Fe33B4,FALSE\nCr13Fe34B3,FALSE\nCr14(Fe3C)9,TRUE\nCr14Fe29C7,FALSE\nCr14FeB5,TRUE\nCr15Co24C11,FALSE\nCr15Co26C9,TRUE\nCr15Fe26C9,TRUE\nCr15Fe71B14,TRUE\nCr15Fe73B12,TRUE\nCr15Fe77B8,FALSE\nCr15Fe79B6,FALSE\nCr15Fe81B4,FALSE\nCr15Ni66P19,TRUE\nCr16Fe25C9,TRUE\nCr17(Co2C)11,TRUE\nCr17(Co8C3)3,TRUE\nCr18Fe23C9,TRUE\nCr19(Ni5Mo22)3,FALSE\nCr19Co20C11,TRUE\nCr19Co22C9,TRUE\nCr19Ni62Mo19,TRUE\nCr2(Fe5B)3,TRUE\nCr2(Fe5C)3,FALSE\nCr2(Ge3Pd13)3,TRUE\nCr2.5Fe77.5B20,TRUE\nCr2.5Fe80.5B17,TRUE\nCr2.5Fe82.5B15,TRUE\nCr20(Co7C3)3,TRUE\nCr20(Fe7C3)3,TRUE\nCr20Fe23C7,FALSE\nCr20Ni61P19,TRUE\nCr21Co18C11,TRUE\nCr22(Ni7Mo19)3,TRUE\nCr22Co19C9,TRUE\nCr22Ni17Mo61,FALSE\nCr23(Fe5P2)11,TRUE\nCr23Co20C7,FALSE\nCr23Ni17Mo10,TRUE\nCr23Ni34Mo43,TRUE\nCr24(NiMo)13,TRUE\nCr24.5Fe56B19.5,TRUE\nCr24Co17C9,TRUE\nCr24Fe55B21,TRUE\nCr24Fe56.5P19.5,TRUE\nCr24Ni11Mo15,TRUE\nCr25Fe57.5B17.5,TRUE\nCr25Fe57.5P17.5,TRUE\nCr25Ni56P19,TRUE\nCr26Fe59.5P14.5,TRUE\nCr26Fe60.5P13.5,TRUE\nCr26Ni19Mo5,TRUE\nCr27Fe62B11,TRUE\nCr27Ni15Mo8,TRUE\nCr27Ni8Mo15,TRUE\nCr2Co18B5,TRUE\nCr2Co2B,TRUE\nCr2Co2C,TRUE\nCr2Fe18B5,TRUE\nCr2Fe18P5,TRUE\nCr2Fe21B2,TRUE\nCr2Fe22B,TRUE\nCr2Fe2B,TRUE\nCr2Fe7B,FALSE\nCr2Ni2P,TRUE\nCr3(Fe10B)2,FALSE\nCr30Ni51P19,TRUE\nCr32Ni43Mo25,TRUE\nCr35Ni27Mo38,TRUE\nCr38Ni37Mo25,TRUE\nCr39Ni28Mo33,TRUE\nCr3Co13B4,TRUE\nCr3Co5B2,TRUE\nCr3Fe13B4,TRUE\nCr3Fe14B3,TRUE\nCr3Fe15B2,FALSE\nCr3Fe15C2,FALSE\nCr3Fe21B,FALSE\nCr3Fe37B10,TRUE\nCr3Fe37P10,TRUE\nCr3Fe5B2,TRUE\nCr3Ge18Pd79,TRUE\nCr3Ni13P4,TRUE\nCr3Ni5B2,TRUE\nCr3Ni77P20,TRUE\nCr3NiP,TRUE\nCr3Si10Pd37,TRUE\nCr3Si20Pd77,TRUE\nCr4(Fe27B5)3,TRUE\nCr40Fe47C13,FALSE\nCr42Ni31Mo27,TRUE\nCr43.5Ni40.5P16,TRUE\nCr4Fe13B3,TRUE\nCr4Fe19B2,FALSE\nCr4Fe20B,FALSE\nCr4Fe41B5,FALSE\nCr4Fe43B3,TRUE\nCr4Fe45B,TRUE\nCr4P,FALSE\nCr5(Fe13B2)3,TRUE\nCr5(Fe14B)3,TRUE\nCr5(Fe4B)3,TRUE\nCr5(Fe4B)4,TRUE\nCr5(Fe4B)9,TRUE\nCr5(Fe9B)2,FALSE\nCr5(Fe9C)2,FALSE\nCr5(Ni4P)19,TRUE\nCr53Ni18Mo29,TRUE\nCr55.93Ni28.93P15.14,TRUE\nCr56Ni39Mo5,TRUE\nCr58(Ni9P5)3,TRUE\nCr59.81Ni25.31P14.88,TRUE\nCr5Co11B4,TRUE\nCr5Co3B2,TRUE\nCr5Fe11B4,TRUE\nCr5Fe17B3,TRUE\nCr5Fe19B,FALSE\nCr5Fe37B8,TRUE\nCr5Fe38B7,TRUE\nCr5Fe41B4,TRUE\nCr5Fe43B2,TRUE\nCr5Fe44B,TRUE\nCr5Fe77B18,TRUE\nCr5Fe79B16,TRUE\nCr5Fe81B14,TRUE\nCr5Fe83B12,TRUE\nCr5Fe87B8,FALSE\nCr5Fe89B6,FALSE\nCr5Fe91B4,FALSE\nCr5Ge18Pd77,TRUE\nCr5Ni11B4,TRUE\nCr5Ni3P2,TRUE\nCr6.6Fe79B14.4,TRUE\nCr69.6Ni16.2P14.2,FALSE\nCr6Co14C5,FALSE\nCr6Co15C4,FALSE\nCr6Fe11B3,TRUE\nCr6Fe16B3,TRUE\nCr6Fe17B2,FALSE\nCr6Fe39B5,FALSE\nCr6Fe41B3,FALSE\nCr6Fe43B,FALSE\nCr7(Co7C2)2,FALSE\nCr7(Fe26B5)3,TRUE\nCr7(Ge6Pd25)3,TRUE\nCr7.5Co67.5B25,TRUE\nCr72.5Ni13.5P14,FALSE\nCr73Fe10P17,TRUE\nCr74Fe9P17,TRUE\nCr7Co13C5,TRUE\nCr7Fe34B9,TRUE\nCr7Fe35B8,TRUE\nCr7Fe36B7,TRUE\nCr7Fe37B6,TRUE\nCr7Fe38B5,FALSE\nCr7Fe39B4,FALSE\nCr7Fe40B3,FALSE\nCr7Fe41B2,FALSE\nCr7Fe42B,FALSE\nCr7Fe76P17,TRUE\nCr7Fe77B16,TRUE\nCr7Fe79B14,TRUE\nCr7Fe9B4,TRUE\nCr7Ni34P9,TRUE\nCr7Ni73P20,TRUE\nCr7NiP2,FALSE\nCr7Si20Pd73,TRUE\nCr8(Fe13B)3,FALSE\nCr85(Fe2B3)3,TRUE\nCr87P13,FALSE\nCr8Co12C5,TRUE\nCr8Co13C4,FALSE\nCr8Fe41B,FALSE\nCr9(Co3C)4,FALSE\nCr9Co11C5,TRUE\nCr9Co7B4,TRUE\nCr9Fe35B6,TRUE\nCr9Fe36B5,FALSE\nCr9Fe37B4,FALSE\nCr9Fe38B3,FALSE\nCr9Fe76B15,TRUE\nCr9Ni31P10,TRUE\nCrCo3B,TRUE\nCrCo7B2,TRUE\nCrCo7P2,TRUE\nCrFe15B4,TRUE\nCrFe16B3,TRUE\nCrFe17B2,FALSE\nCrFe18C,FALSE\nCrFe19B5,TRUE\nCrFe19P5,TRUE\nCrFe39P10,TRUE\nCrFe3B,TRUE\nCrFe79B20,TRUE\nCrFe7B2,TRUE\nCrFe8B,FALSE\nCrNi15P4,TRUE\nCrNi3B,TRUE\nCrNi3P,TRUE\nCrNi7B2,TRUE\nCrNi7P2,TRUE\nCrSi10Pd39,TRUE\nCrSi20Pd79,TRUE\nCrSi4Pd15,TRUE\nCrSi5Pd19,TRUE\nCu(Ni25P8)3,FALSE\nCu(Ni5P)4,FALSE\nCu1.7Si16.5Pd81.8,TRUE\nCu10Si15.8Pd74.2,TRUE\nCu10Si16.5Pd73.5,TRUE\nCu10Si17Pd73,TRUE\nCu11Si19.5Pd69.5,TRUE\nCu12.5Si16.5Pd71,TRUE\nCu12.5Si17Pd70.5,TRUE\nCu12Ni67P21,FALSE\nCu12Si15.5Pd72.5,TRUE\nCu13(Ni22P7)3,FALSE\nCu13(Ni23P6)3,FALSE\nCu13Ag12,FALSE\nCu13Ni67P20,FALSE\nCu14.4Ni65.6P20,TRUE\nCu14.5Si16.5Pd69,TRUE\nCu14Si15.1Pd70.9,TRUE\nCu15Si16.5Pd68.5,TRUE\nCu15Si16Pd69,TRUE\nCu16.5Si16.5Pd67,TRUE\nCu19Si16.5Pd64.5,TRUE\nCu2(Ni13P3)3,TRUE\nCu20.9Si16.5Pd62.6,TRUE\nCu26.7Si16.5Pd56.8,FALSE\nCu2Ag2Ge,TRUE\nCu2Ni18P5,TRUE\nCu2Ni37P11,TRUE\nCu2Si17.25Pd80.75,TRUE\nCu3.5Si16.5Pd80,TRUE\nCu37.5Ag37.5Ge25,TRUE\nCu38.75Ag38.75Ge22.5,TRUE\nCu3Ni17P5,TRUE\nCu3Ni36P11,TRUE\nCu3Ni37P10,TRUE\nCu3Ni38P9,TRUE\nCu3Ni73P24,FALSE\nCu3Ni80B17,TRUE\nCu3Ni81P16,FALSE\nCu3Si17Pd80,TRUE\nCu4.2Si16.5Pd79.3,TRUE\nCu4.5Si18Pd77.5,TRUE\nCu4Ni35P11,TRUE\nCu4Ni37P9,TRUE\nCu4Si16.5Pd79.5,TRUE\nCu4Si16.9Pd79.1,TRUE\nCu4Si9Pd37,TRUE\nCu5(Ni4P)9,TRUE\nCu5.7Si20.5Pd73.8,TRUE\nCu5.8Si19.5Pd74.7,TRUE\nCu5.9Si17.5Pd76.6,TRUE\nCu5.9Si18.5Pd75.6,TRUE\nCu52.8Ni27.2P20,TRUE\nCu5Ni34P11,TRUE\nCu6(SiPd3)11,TRUE\nCu6.1Si15.5Pd78.4,TRUE\nCu6.7Si16.5Pd76.8,TRUE\nCu61.6Ni18.4P20,TRUE\nCu67Ni17P16,TRUE\nCu69Ni13P18,TRUE\nCu6Si16.5Pd77.5,TRUE\nCu73Ag27,FALSE\nCu73Ni11P16,TRUE\nCu78.5Ag14P7.5,FALSE\nCu7Ni33P10,FALSE\nCu7Ni34P9,FALSE\nCu7Si16.5Pd76.5,TRUE\nCu7Si17Pd76,TRUE\nCu7Si20Pd73,TRUE\nCu80.3Ag12.2P7.5,TRUE\nCu80.5Ag10.5P9,FALSE\nCu80.8Ag12.2P7,TRUE\nCu81.5Ag10.5P8,TRUE\nCu81.5Ag12.2P6.3,FALSE\nCu81.9Ag10.5P7.6,TRUE\nCu82.5Ag10.5P7,TRUE\nCu82.5Ag9P8.5,FALSE\nCu82.8Ag9P8.2,TRUE\nCu83.5Ag8.9P7.6,TRUE\nCu84.5Ag7P8.5,FALSE\nCu84.5Ag9P6.5,FALSE\nCu84Ag9P7,TRUE\nCu85(Ag3P2)3,FALSE\nCu85.2Ag7.1P7.7,TRUE\nCu85.5Ag7.5P7,TRUE\nCu86Ag7.5P6.5,FALSE\nCu87Ag5.5P7.5,FALSE\nCu8Si16.2Pd75.8,TRUE\nCu9Si16Pd75,TRUE\nCuNi19P5,TRUE\nCuNi37P12,FALSE\nCuNi38P11,TRUE\nCuNi39P10,TRUE\nCuNi40P9,TRUE\nCuNi41P8,FALSE\nCuNi7P2,TRUE\nCuNi83P16,FALSE\nCuSi2Pd7,TRUE\nDy0.3Zr10Fe89.7,TRUE\nDy42Zr5Fe3,FALSE\nDy44Zr5Fe,TRUE\nEr67.5B10Au22.5,TRUE\nFe(CuAg)2,FALSE\nFe1.7Si16.5Pd81.8,TRUE\nFe10B19N21,TRUE\nFe10Si16.5Pd73.5,TRUE\nFe12.3Ni64.7B23,TRUE\nFe12.5Si16.5Pd71,TRUE\nFe12.5Si6B81.5,FALSE\nFe12Ag13,FALSE\nFe12B5F3,TRUE\nFe12B7F,TRUE\nFe12Cu3Ag10,FALSE\nFe13Ag12,FALSE\nFe13B4F3,TRUE\nFe13B7,TRUE\nFe13Cu47Ag40,FALSE\nFe13Ni2B5,TRUE\nFe13Ni5B2,FALSE\nFe13Si20Pd67,TRUE\nFe13Si2C5,TRUE\nFe13Si3B4,TRUE\nFe13Si3C4,TRUE\nFe13Si4C3,TRUE\nFe13Si5C2,TRUE\nFe14(SiB)3,TRUE\nFe14(SiC)3,TRUE\nFe14Cu55Ag31,FALSE\nFe15B2Mo3,TRUE\nFe15B4Mo,TRUE\nFe15CoB4,TRUE\nFe15Cu22Ag13,FALSE\nFe15Cu3B2,FALSE\nFe15CuB4,FALSE\nFe15Ni3B2,FALSE\nFe15NiB4,TRUE\nFe15P2C3,TRUE\nFe15P3C2,TRUE\nFe15P4C,TRUE\nFe15Si16.5Pd68.5,FALSE\nFe15Si2B3,TRUE\nFe15Si3B2,TRUE\nFe15SiB4,TRUE\nFe16.5Co66.5B17,TRUE\nFe16B3C,TRUE\nFe16B3P,TRUE\nFe16B4Mo5,TRUE\nFe16Cu5B4,FALSE\nFe16GeB3,TRUE\nFe16Ni5B4,TRUE\nFe16P3C,TRUE\nFe16PC3,FALSE\nFe16Si3B,TRUE\nFe16SiB3,TRUE\nFe16SiP3,TRUE\nFe16W4C5,FALSE\nFe17(Cu5Ag6)3,FALSE\nFe17B2C,TRUE\nFe17B2Mo,FALSE\nFe17B3,TRUE\nFe17B3Mo5,TRUE\nFe17Cu5B3,FALSE\nFe17Cu8,FALSE\nFe17CuB2,FALSE\nFe17Ni5B3,TRUE\nFe17NiB2,TRUE\nFe17P2C,FALSE\nFe17W3C5,TRUE\nFe18.5Ni54.5B27,TRUE\nFe18B2Mo5,FALSE\nFe18B5Mo2,TRUE\nFe18B5W2,TRUE\nFe18Ni53B29,TRUE\nFe18Ni5B2,FALSE\nFe18Si4B3,TRUE\nFe18W2C5,FALSE\nFe19(B2Mo)2,TRUE\nFe19(BMo)3,TRUE\nFe19.5Ni58.5B22,TRUE\nFe19B,FALSE\nFe19B5Mo,TRUE\nFe19B5P,TRUE\nFe19B5W,TRUE\nFe19B6,TRUE\nFe19BMo5,FALSE\nFe19CoB5,TRUE\nFe19Ni19B12,TRUE\nFe19Ni21B10,TRUE\nFe19Ni5B,FALSE\nFe19WC5,FALSE\nFe20(Ni7B3)3,TRUE\nFe20.5Ni60.5B19,TRUE\nFe20B2Mo3,FALSE\nFe20B2P3,TRUE\nFe20B3Mo2,TRUE\nFe20B3P2,TRUE\nFe20B4C,TRUE\nFe20B4P,TRUE\nFe20BF4,FALSE\nFe20BP4,TRUE\nFe20Cu11Ag19,TRUE\nFe20Cu49Ag31,FALSE\nFe20Ge2B3,TRUE\nFe20Si2B3,TRUE\nFe20Si2P3,TRUE\nFe20SiP4,TRUE\nFe20WC4,FALSE\nFe21B4,TRUE\nFe21BMo3,FALSE\nFe21BP3,FALSE\nFe21Co62B17,TRUE\nFe21Cu15Ag14,TRUE\nFe21Cu6Ag23,TRUE\nFe21Ni21B8,TRUE\nFe21Ni59B20,TRUE\nFe21Ni61.5B17.5,TRUE\nFe21Ni62.5B16.5,TRUE\nFe21Ni62B17,TRUE\nFe21SiB3,TRUE\nFe22B3,TRUE\nFe22BMo2,FALSE\nFe22Cu29Ag49,FALSE\nFe22Ni59B19,TRUE\nFe23Cu27,FALSE\nFe23Ni59B18,TRUE\nFe23Ni60B17,TRUE\nFe24Ni59B17,TRUE\nFe25Ni59B16,TRUE\nFe27Cu45Ag28,FALSE\nFe27Cu51Ag22,FALSE\nFe28B9F13,FALSE\nFe29.5Ni50.5B20,TRUE\nFe29Ag21,FALSE\nFe29B7F14,FALSE\nFe29Co54B17,TRUE\nFe29Cu71,FALSE\nFe29Cu8Ag63,FALSE\nFe2Co2B,TRUE\nFe2Cu83Ag15,FALSE\nFe2CuAg,FALSE\nFe2Ni2B,TRUE\nFe2Ni2P,TRUE\nFe30.5Ni50.5B19,TRUE\nFe30B19F,TRUE\nFe31.5Ni50.5B18,TRUE\nFe31Cu10B9,FALSE\nFe31Mo10C9,TRUE\nFe31Ni10B9,TRUE\nFe31W10C9,FALSE\nFe31W8C11,FALSE\nFe32.5Ni50.5B17,TRUE\nFe32Cu37Ag31,FALSE\nFe32W7C11,TRUE\nFe33.5Ni50.5B16,TRUE\nFe33Ag67,FALSE\nFe33B12N5,TRUE\nFe33B7Mo10,TRUE\nFe33Cu10B7,FALSE\nFe33Mo8C9,TRUE\nFe33Ni10B7,TRUE\nFe33Ni50B17,TRUE\nFe33Ni5B12,TRUE\nFe33W10C7,FALSE\nFe33W6C11,TRUE\nFe33W7C10,TRUE\nFe33W8C9,FALSE\nFe34W5C11,TRUE\nFe34W7C9,FALSE\nFe35(B2Mo3)3,TRUE\nFe35(Mo2C3)3,TRUE\nFe35(Si3B2)3,TRUE\nFe35(W2C3)3,FALSE\nFe35W4C11,FALSE\nFe35W8C7,FALSE\nFe36.5Ni36.5B27,TRUE\nFe36B5Mo9,TRUE\nFe36Cu13Ag51,FALSE\nFe36Cu23Ag41,TRUE\nFe36Cu49Ag15,FALSE\nFe36Cu5B9,FALSE\nFe36Ni5B9,TRUE\nFe36Si5B9,TRUE\nFe37(Cu2Ag)21,FALSE\nFe37Ag63,FALSE\nFe37B10Mo3,TRUE\nFe37B10N3,TRUE\nFe37B3Mo10,FALSE\nFe37B4Mo9,FALSE\nFe37B7Mo6,TRUE\nFe37Cu41Ag22,FALSE\nFe37Cu5B8,FALSE\nFe37Cu63,FALSE\nFe37Mo4C9,TRUE\nFe37Ni10B3,FALSE\nFe37Ni37B26,TRUE\nFe37Ni5B8,TRUE\nFe37Si5B8,TRUE\nFe37SiB12,FALSE\nFe37W2C11,FALSE\nFe37W4C9,FALSE\nFe37W6C7,FALSE\nFe37W8C5,FALSE\nFe38(BMo3)3,FALSE\nFe38(CuAg)31,TRUE\nFe38(Mo3C)3,TRUE\nFe38.5Ni38.5B23,TRUE\nFe38B7Mo5,TRUE\nFe38Cu5B7,FALSE\nFe38Ni5B7,TRUE\nFe38SiB11,FALSE\nFe39Ag61,FALSE\nFe39B10Mo,TRUE\nFe39B11,TRUE\nFe39B2Mo9,FALSE\nFe39B5F6,TRUE\nFe39B5Mo6,TRUE\nFe39B6Mo5,TRUE\nFe39B7Mo4,TRUE\nFe39BMo10,FALSE\nFe39Cu5B6,FALSE\nFe39Ni10B,FALSE\nFe39Ni39B22,TRUE\nFe39Ni42B19,TRUE\nFe39Ni5B6,TRUE\nFe39Si2B9,TRUE\nFe39Si4B7,TRUE\nFe39Si5B6,TRUE\nFe39SiB10,TRUE\nFe39W2C9,FALSE\nFe39W4C7,FALSE\nFe39W6C5,FALSE\nFe3Ag7,FALSE\nFe3B,TRUE\nFe3Co37B10,TRUE\nFe3Co5B2,TRUE\nFe3CoB,TRUE\nFe3Cu7,FALSE\nFe3Ni13B4,TRUE\nFe3Ni13P4,TRUE\nFe3Ni5B2,TRUE\nFe3Ni5P2,TRUE\nFe3Ni77P20,TRUE\nFe3NiB,TRUE\nFe3NiP,TRUE\nFe4(CuAg)3,TRUE\nFe4.2Si16.5Pd79.3,TRUE\nFe40.5Ni40B19.5,TRUE\nFe40B3P7,TRUE\nFe40B7P3,TRUE\nFe40B9C,TRUE\nFe40B9P,TRUE\nFe40B9Pd,TRUE\nFe40BMo9,FALSE\nFe40Cu31Ag29,FALSE\nFe40GeB9,TRUE\nFe40Si3P7,TRUE\nFe40SiB9,TRUE\nFe40SiP9,TRUE\nFe41(B2P)3,TRUE\nFe41(BMo2)3,FALSE\nFe41(BP2)3,TRUE\nFe41(SiB2)3,TRUE\nFe41(W2C)3,FALSE\nFe41.5Co41.5B17,TRUE\nFe41.5Ni41B17.5,TRUE\nFe41B4Mo5,FALSE\nFe41B4P5,TRUE\nFe41B5Mo4,TRUE\nFe41B8F,TRUE\nFe41B9,TRUE\nFe41Cu30Ag29,TRUE\nFe41Cu5B4,FALSE\nFe41Ni41B18,TRUE\nFe41Ni42B17,TRUE\nFe41Ni5B4,FALSE\nFe41Si2B7,TRUE\nFe41SiB8,TRUE\nFe41W2C7,FALSE\nFe41W4C5,FALSE\nFe42B33N25,TRUE\nFe42B3Mo5,FALSE\nFe42B3P5,FALSE\nFe42Cu31Ag27,FALSE\nFe42Cu41Ag17,FALSE\nFe42Cu5B3,FALSE\nFe42Ni5B3,FALSE\nFe42SiB7,TRUE\nFe43B2Mo5,FALSE\nFe43B3Mo4,FALSE\nFe43B6N,TRUE\nFe43B7,TRUE\nFe43BMo6,FALSE\nFe43Cu5B2,FALSE\nFe43Ni40B17,TRUE\nFe43Ni43B14,TRUE\nFe43Ni5B2,FALSE\nFe43W2C5,FALSE\nFe43W4C3,FALSE\nFe44BMo5,FALSE\nFe44Ni5B,FALSE\nFe45BMo4,FALSE\nFe45Cu31Ag24,FALSE\nFe45W2C3,FALSE\nFe46.2Ni30.8B23,TRUE\nFe48Ni35B17,TRUE\nFe4Ag21,FALSE\nFe4B,TRUE\nFe4Cu15Ag31,FALSE\nFe4Ni16P5,TRUE\nFe4P,TRUE\nFe5.1Si16.8Pd78.1,TRUE\nFe50Co33B17,TRUE\nFe50Ni33B17,TRUE\nFe51Cu23Ag26,FALSE\nFe51Cu38Ag11,FALSE\nFe52.5B24.5N23,TRUE\nFe53.5Ni18B28.5,TRUE\nFe53Ni30B17,TRUE\nFe54.5Ni18.5B27,TRUE\nFe54Ni29B17,TRUE\nFe55Cu32Ag13,FALSE\nFe56Ni19B25,TRUE\nFe57Cu6Ag37,FALSE\nFe57Ni19B24,TRUE\nFe57Ni25B18,TRUE\nFe58.5Ni20B21.5,TRUE\nFe58Co25B17,TRUE\nFe59.5Ni20B20.5,TRUE\nFe59B10F31,FALSE\nFe59B8F33,FALSE\nFe59Mo17C24,TRUE\nFe59Ni25B16,TRUE\nFe5Co3B2,TRUE\nFe5Cu16Ag29,FALSE\nFe5Ni11P4,TRUE\nFe5Ni3B2,TRUE\nFe6.7Si16.5Pd76.8,TRUE\nFe60.1Ni16.9B23,TRUE\nFe60B7F33,FALSE\nFe61.5Ni22B16.5,TRUE\nFe61B39,TRUE\nFe61Co22B17,TRUE\nFe61Ni20B19,TRUE\nFe61Ni25B14,TRUE\nFe63B37,TRUE\nFe63Cu20Ag17,FALSE\nFe63Mo17C20,TRUE\nFe63Ni20B17,TRUE\nFe63Ni25B12,FALSE\nFe64B29N7,TRUE\nFe64Co19B17,TRUE\nFe65B17.5F17.5,TRUE\nFe65B22.5F12.5,TRUE\nFe65B31.5F3.5,TRUE\nFe65Si12.5C22.5,TRUE\nFe65Si17.5C17.5,TRUE\nFe65Si22.5C12.5,TRUE\nFe66.4Ni16.6B17,TRUE\nFe66.5Co16.5B17,TRUE\nFe67(Cu5B6)3,FALSE\nFe67(Ni5B6)3,TRUE\nFe67.5Si10B22.5,TRUE\nFe67.5Si12.5B20,TRUE\nFe67.5Si15B17.5,TRUE\nFe67.5Si17.5B15,TRUE\nFe67Cu10Ag23,FALSE\nFe67Mo17C16,TRUE\nFe67Ni25B8,FALSE\nFe67Si13B20,TRUE\nFe69B16Mo15,TRUE\nFe69Cu15B16,FALSE\nFe69Ni15B16,TRUE\nFe69Ni25B6,FALSE\nFe69Si7B24,TRUE\nFe6B9Mo85,TRUE\nFe6B9W85,TRUE\nFe6Co77B17,TRUE\nFe6Co85B9,TRUE\nFe6Cu19,FALSE\nFe6Ni85B9,TRUE\nFe70(Si3B7)3,TRUE\nFe70Si12.5B17.5,TRUE\nFe70Si12.5C17.5,TRUE\nFe70Si13B17,TRUE\nFe70Si17.5B12.5,TRUE\nFe70Si17.5C12.5,TRUE\nFe70Si7.5B22.5,TRUE\nFe71.5Co11.5B17,TRUE\nFe71B14Mo15,TRUE\nFe71B29,TRUE\nFe71Cu15B14,FALSE\nFe71Mo17C12,TRUE\nFe71Ni15B14,TRUE\nFe71Ni25B4,FALSE\nFe71Si7B22,TRUE\nFe72(SiB3)7,TRUE\nFe72.5P10C17.5,TRUE\nFe72.5P12.5C15,TRUE\nFe72.5P15C12.5,TRUE\nFe72.5P17.5C10,TRUE\nFe72.5P20C7.5,TRUE\nFe72.5Si10B17.5,TRUE\nFe72.5Si12.5B15,TRUE\nFe72.5Si15B12.5,TRUE\nFe72.5Si17.5B10,TRUE\nFe72.5Si5B22.5,TRUE\nFe72.5Si7.5B20,TRUE\nFe72Si13B15,TRUE\nFe73(B4Mo5)3,TRUE\nFe73(Cu5B4)3,FALSE\nFe73(Ni5B4)3,TRUE\nFe73(SiB8)3,FALSE\nFe73.5B20W6.5,TRUE\nFe73B20Mo7,TRUE\nFe73Co10B17,TRUE\nFe73Ni10B17,TRUE\nFe73Ni25B2,FALSE\nFe73Si9.5B17.5,TRUE\nFe73W10C17,FALSE\nFe74.5Si10.5B15,TRUE\nFe74.5Si18B7.5,FALSE\nFe74.8Si13B12.2,TRUE\nFe74.9Si7.3B17.8,TRUE\nFe74Mo9P17,TRUE\nFe75.3Si9.7B15,TRUE\nFe75.5Co7.5B17,TRUE\nFe75B11P14,FALSE\nFe75B18F7,TRUE\nFe75B19P6,FALSE\nFe75B21P4,TRUE\nFe75Mo17C8,TRUE\nFe75P12.5C12.5,TRUE\nFe75P17.5C7.5,TRUE\nFe75P7.5C17.5,TRUE\nFe75Si12.5B12.5,TRUE\nFe75Si12B13,TRUE\nFe75Si13B12,TRUE\nFe75Si17.5B7.5,TRUE\nFe75Si3B22,TRUE\nFe75Si4B21,TRUE\nFe75Si7.5B17.5,TRUE\nFe76(P5C3)3,TRUE\nFe76Mo7P17,TRUE\nFe76Ni5B19,TRUE\nFe77.5B20W2.5,TRUE\nFe77.5B22.5,TRUE\nFe77.5P10C12.5,TRUE\nFe77.5P12.5C10,TRUE\nFe77.5P15C7.5,TRUE\nFe77.5P16C6.5,TRUE\nFe77.5P17.5C5,TRUE\nFe77.5P5C17.5,FALSE\nFe77.5P7.5C15,TRUE\nFe77.5Si10B12.5,TRUE\nFe77.5Si12.5B10,TRUE\nFe77.5Si13.5B9,TRUE\nFe77.5Si15B7.5,TRUE\nFe77.5Si2.5B20,TRUE\nFe77.5Si5B17.5,TRUE\nFe77.5Si7.5B15,TRUE\nFe77B10F13,TRUE\nFe77B13P10,TRUE\nFe77B15P8,TRUE\nFe77B17P6,TRUE\nFe77B19P4,FALSE\nFe77B20Mo3,TRUE\nFe77B8Mo15,FALSE\nFe77Co6B17,TRUE\nFe77Cu15B8,FALSE\nFe77Cu5B18,FALSE\nFe77Ni15B8,FALSE\nFe77Ni5B18,TRUE\nFe77P15C8,TRUE\nFe77Si11B12,TRUE\nFe78.5B20F1.5,TRUE\nFe78.5P15C6.5,TRUE\nFe78.5Si9B12.5,TRUE\nFe78B17C5,TRUE\nFe78B9P13,TRUE\nFe78Si15B7,TRUE\nFe78Si7.5B14.5,TRUE\nFe78Si7B15,TRUE\nFe79(B2C)7,TRUE\nFe79(B2Mo5)3,FALSE\nFe79(B2P)7,TRUE\nFe79(B2P5)3,TRUE\nFe79(B2W)7,TRUE\nFe79(B3P4)3,TRUE\nFe79(B4C3)3,TRUE\nFe79(B4P3)3,TRUE\nFe79(B5P2)3,TRUE\nFe79(B6C)3,TRUE\nFe79(B6P)3,FALSE\nFe79(BP2)7,TRUE\nFe79(BP6)3,TRUE\nFe79(Cu5B2)3,FALSE\nFe79(Ni5B2)3,FALSE\nFe79(SiB2)7,TRUE\nFe79(W2C)7,FALSE\nFe79.5Cu0.5B20,TRUE\nFe79.5Si3.5B17,TRUE\nFe79B10F11,TRUE\nFe79B10P11,TRUE\nFe79B11P10,TRUE\nFe79B13P8,TRUE\nFe79B16Mo5,TRUE\nFe79B16P5,TRUE\nFe79B17P4,TRUE\nFe79B20Mo,TRUE\nFe79B20W,TRUE\nFe79B21,TRUE\nFe79B8P13,TRUE\nFe79Co4B17,TRUE\nFe79Cu5B16,FALSE\nFe79CuB20,FALSE\nFe79Ni5B16,TRUE\nFe79W16C5,FALSE\nFe7B2Mo,TRUE\nFe7BMo2,TRUE\nFe7CoB2,TRUE\nFe7CuB2,FALSE\nFe7Ni2B,FALSE\nFe7Ni76B17,TRUE\nFe7Ni7B6,TRUE\nFe7Ni9B4,TRUE\nFe7Ni9P4,TRUE\nFe7NiB2,TRUE\nFe7Si20Pd73,TRUE\nFe7Si2B,TRUE\nFe7Si2C,TRUE\nFe7SiB2,TRUE\nFe7SiC2,TRUE\nFe7WC2,FALSE\nFe80.5B17Mo2.5,TRUE\nFe80.5B17W2.5,TRUE\nFe80.5Ni2.5B17,TRUE\nFe80.5P13C6.5,TRUE\nFe80.5P15C4.5,TRUE\nFe80B11C9,TRUE\nFe80B11P9,TRUE\nFe80B13C7,TRUE\nFe80B13P7,TRUE\nFe80B17C3,TRUE\nFe80B17P3,FALSE\nFe80B7P13,TRUE\nFe80B9C11,TRUE\nFe80B9P11,TRUE\nFe80Co3B17,TRUE\nFe80Ni3B17,TRUE\nFe80P12.5C7.5,TRUE\nFe80P13C7,TRUE\nFe80P17.5C2.5,TRUE\nFe80P7.5C12.5,TRUE\nFe80Si10.5P9.5,TRUE\nFe80Si11B9,FALSE\nFe80Si12.5B7.5,TRUE\nFe80Si2.5B17.5,TRUE\nFe80Si2.5P17.5,TRUE\nFe80Si3B17,TRUE\nFe80Si7.5B12.5,TRUE\nFe80Si7P13,TRUE\nFe80Si9P11,TRUE\nFe81.5B18.5,TRUE\nFe81.5Cu0.5B18,TRUE\nFe81.5Cu1.5B17,TRUE\nFe81.5P15C3.5,TRUE\nFe81.5Si12.5B6,FALSE\nFe81.5Si4B14.5,TRUE\nFe81B10C9,TRUE\nFe81B10P9,TRUE\nFe81B12C7,TRUE\nFe81B12Mo7,TRUE\nFe81B12P7,TRUE\nFe81B12W7,TRUE\nFe81B14C5,TRUE\nFe81B14Mo5,TRUE\nFe81B14P5,TRUE\nFe81B16C3,TRUE\nFe81B16P3,TRUE\nFe81B17F2,TRUE\nFe81B19,TRUE\nFe81B4Mo15,FALSE\nFe81B6P13,TRUE\nFe81B7P12,TRUE\nFe81B8P11,TRUE\nFe81B9P10,TRUE\nFe81Co2B17,TRUE\nFe81Cu3B16,FALSE\nFe81Cu5B14,FALSE\nFe81CuB18,FALSE\nFe81Ni15B4,FALSE\nFe81Ni3B16,TRUE\nFe81Ni5B14,TRUE\nFe81Si4B15,TRUE\nFe82(BC)9,TRUE\nFe82(BP)9,TRUE\nFe82(SiB5)3,TRUE\nFe82.5B17.5,TRUE\nFe82.5P10C7.5,FALSE\nFe82.5P12.5C5,FALSE\nFe82.5P15C2.5,TRUE\nFe82.5P7.5C10,FALSE\nFe82.5Si10B7.5,FALSE\nFe82.5Si5B12.5,TRUE\nFe82B11C7,TRUE\nFe82B7P11,TRUE\nFe82CoB17,TRUE\nFe82P11.5C6.5,TRUE\nFe82Si5B13,TRUE\nFe82SiB17,TRUE\nFe82Sn1.5B16.5,TRUE\nFe83.5Cu0.5B16,TRUE\nFe83.5Si6.5B10,FALSE\nFe83B10C7,TRUE\nFe83B10P7,TRUE\nFe83B12C5,TRUE\nFe83B12Mo5,TRUE\nFe83B12P5,TRUE\nFe83B14C3,TRUE\nFe83B14P3,TRUE\nFe83B17,TRUE\nFe83B2.3P14.7,TRUE\nFe83B2Mo15,FALSE\nFe83B3P14,FALSE\nFe83B5P12,TRUE\nFe83B6P11,TRUE\nFe83B7P10,TRUE\nFe83B8C9,TRUE\nFe83B8P9,TRUE\nFe83B9Mo8,FALSE\nFe83Cu3B14,FALSE\nFe83Cu5B12,FALSE\nFe83CuB16,FALSE\nFe83Ni15B2,FALSE\nFe83Ni3B14,TRUE\nFe83Ni5B12,FALSE\nFe83NiB16,TRUE\nFe83Si11B6,FALSE\nFe83Si2B15,TRUE\nFe83Si3B14,TRUE\nFe83Si4B13,TRUE\nFe83Si5B12,TRUE\nFe83Si7B10,FALSE\nFe83Si8B9,FALSE\nFe83SiB16,TRUE\nFe84B11C5,TRUE\nFe84B5P11,FALSE\nFe84B7P9,FALSE\nFe84Si3B13,TRUE\nFe84SiB15,TRUE\nFe85(B4C)3,TRUE\nFe85(CuB4)3,FALSE\nFe85(NiB4)3,FALSE\nFe85.5Cu0.5B14,TRUE\nFe85B11P4,FALSE\nFe85B7Mo8,FALSE\nFe85B8C7,TRUE\nFe85CuB14,FALSE\nFe85NiB14,TRUE\nFe85P12.5C2.5,FALSE\nFe85P7.5C7.5,FALSE\nFe85Si2B13,FALSE\nFe86(BC)7,TRUE\nFe86.5Cu0.5B13,TRUE\nFe87B13,TRUE\nFe87B8Mo5,FALSE\nFe87Cu3B10,FALSE\nFe87Cu5B8,FALSE\nFe87CuB12,FALSE\nFe87Ni5B8,FALSE\nFe87NiB12,FALSE\nFe89B6F5,FALSE\nFe89B6Mo5,FALSE\nFe89Cu3B8,FALSE\nFe89Cu5B6,FALSE\nFe89CuB10,FALSE\nFe89Ni3B8,FALSE\nFe89Ni5B6,FALSE\nFe89NiB10,FALSE\nFe8BC,TRUE\nFe8BMo,TRUE\nFe8BP,TRUE\nFe8Co75B17,TRUE\nFe8CuB,FALSE\nFe8GeB,TRUE\nFe8NiB,TRUE\nFe8PC,TRUE\nFe8SiB,TRUE\nFe8SiP,TRUE\nFe9(BN)8,TRUE\nFe91(CuB2)3,FALSE\nFe91B4Mo5,FALSE\nFe91B7F2,FALSE\nFe91B9,TRUE\nFe91Cu5B4,FALSE\nFe91CuB8,FALSE\nFe91Ni5B4,FALSE\nFe91NiB8,FALSE\nFe93B2Mo5,FALSE\nFe93CuB6,FALSE\nFe93Ni3B4,FALSE\nFe93NiB6,FALSE\nFe95CuB4,FALSE\nFe95NiB4,FALSE\nFe9Ag11,FALSE\nFeAg,FALSE\nFeB5Mo14,TRUE\nFeB5W14,TRUE\nFeCo14B5,TRUE\nFeCo15B4,TRUE\nFeCo3B,TRUE\nFeCo7B2,TRUE\nFeCu33Ag16,FALSE\nFeCu9,FALSE\nFeNi,TRUE\nFeNi14B5,TRUE\nFeNi15P4,TRUE\nFeNi3B,TRUE\nFeNi3P,TRUE\nFeNi79P20,TRUE\nFeNi7P2,TRUE\nGa10Fe73B17,TRUE\nGa2Fe81B17,TRUE\nGa4Fe79B17,TRUE\nGa6Fe77B17,TRUE\nGa8Fe75B17,TRUE\nGd0.3Zr10Fe89.7,TRUE\nGd11Al5Ni4,TRUE\nGd11Al9,TRUE\nGd12.9Co73Mo14.1,TRUE\nGd14Co70.6Mo15.4,TRUE\nGd14Si11,TRUE\nGd19.4Co72.8Mo7.8,TRUE\nGd2(Al5Ni)3,TRUE\nGd2Al17Ni,TRUE\nGd2Al23,TRUE\nGd2Al7Ni,FALSE\nGd33.3Al33.4Fe33.3,TRUE\nGd3Al13Cu4,TRUE\nGd3Al13Ni4,TRUE\nGd3Al14Ni3,TRUE\nGd3Al15Ni2,FALSE\nGd3Al16Ni,FALSE\nGd3Al17,FALSE\nGd3Al2,TRUE\nGd3Al22,TRUE\nGd3Al47,FALSE\nGd3Au,TRUE\nGd3Zr5Fe42,FALSE\nGd5(Al14Ni)3,TRUE\nGd5.5Al89Fe5.5,TRUE\nGd5Al37Ni8,TRUE\nGd5Al83Ni12,TRUE\nGd5Al87Ni8,TRUE\nGd6.4Al87.2Fe6.4,TRUE\nGd67.5B10Au22.5,TRUE\nGd6Al39Ni5,TRUE\nGd7(Al29Ni2)3,TRUE\nGd7.3Al85.4Fe7.3,TRUE\nGd7Al83Ni10,TRUE\nGd8.2Al83.6Fe8.2,TRUE\nGd8.4Co75.6Mo16,TRUE\nGd8Al85Ni7,TRUE\nGd9.1Al81.8Fe9.1,TRUE\nGd9Al11,TRUE\nGd9Al81Ni10,TRUE\nGd9Al83Ni8,TRUE\nGd9Al85Ni6,TRUE\nGdAl,TRUE\nGdAl15Ni4,FALSE\nGdAl16Ni3,TRUE\nGdAl17Ni2,TRUE\nGdAl18Ni,TRUE\nGdAl3Ni,FALSE\nGdAl7Ni2,TRUE\nGdAl8Fe,TRUE\nGdAl8Ni,TRUE\nGdAl9,TRUE\nGdZr5Fe44,TRUE\nGe21Pd79,TRUE\nHf(Cu2Ni)3,FALSE\nHf(CuNi)2,TRUE\nHf(CuNi2)3,FALSE\nHf10Cu7Ni3,TRUE\nHf10Nb7Si3,TRUE\nHf10V7Si3,TRUE\nHf11(Cu2Ni)3,TRUE\nHf11(CuNi2)3,TRUE\nHf11(Nb2Si)3,TRUE\nHf11(V2Si)3,TRUE\nHf11(Zr2Si)3,TRUE\nHf11Cu4Ni5,TRUE\nHf11Cu5Ni4,TRUE\nHf11Fe54.9O34.1,FALSE\nHf11TaFe38,TRUE\nHf12.2Fe51.5O36.3,FALSE\nHf12Nb5Si3,TRUE\nHf12V5Si3,TRUE\nHf13.7Fe50.2O36.1,TRUE\nHf13Al2Cu5,TRUE\nHf13Al2Ni5,TRUE\nHf13Cu4Ni3,TRUE\nHf13Nb4Si3,TRUE\nHf13Ta17Fe70,TRUE\nHf13V4Si3,TRUE\nHf14(NbSi)3,TRUE\nHf14(VSi)3,TRUE\nHf15.2Zr60.8Fe24,TRUE\nHf15Cu2Ni3,TRUE\nHf15Cu4Ni,FALSE\nHf15Nb2Si3,TRUE\nHf15V2Si3,TRUE\nHf16NbSi3,TRUE\nHf16VSi3,TRUE\nHf17Si3,TRUE\nHf18.2Fe46.2O35.6,TRUE\nHf19(TaFe8)9,TRUE\nHf2(Zr5Si)3,TRUE\nHf2.1Fe88.4O9.5,FALSE\nHf21Nb22Cu57,TRUE\nHf22.8Zr53.2Fe24,TRUE\nHf23Nb20Cu57,TRUE\nHf25Zr32Be43,TRUE\nHf28(Nb5Cu19)3,TRUE\nHf28.8Nb33Cu38.2,TRUE\nHf2Cu2Ni,TRUE\nHf2Cu3,TRUE\nHf2Cu3Ni5,TRUE\nHf2Cu5Ni3,TRUE\nHf2Cu7Ni,FALSE\nHf2CuNi,TRUE\nHf2CuNi2,TRUE\nHf2CuNi7,TRUE\nHf2Ni3,TRUE\nHf2Ta3Fe5,TRUE\nHf2Ta7Fe16,TRUE\nHf30.1Nb30Cu39.9,TRUE\nHf32.3Nb25Cu42.7,TRUE\nHf33Nb10Cu57,TRUE\nHf34.2Zr41.8Fe24,TRUE\nHf34.4Nb20Cu45.6,TRUE\nHf36.6Nb15Cu48.4,TRUE\nHf37Fe63,TRUE\nHf38.7Nb10Cu51.3,TRUE\nHf38Nb5Cu57,TRUE\nHf3Cu2,TRUE\nHf3Cu2Ni5,TRUE\nHf3Cu3Ni4,TRUE\nHf3Cu4Ni3,TRUE\nHf3Cu5Ni2,TRUE\nHf3Cu6Ni,TRUE\nHf3Cu7,TRUE\nHf3CuNi,TRUE\nHf3CuNi6,TRUE\nHf3Ni2,TRUE\nHf3Ni7,TRUE\nHf3Ta2Fe5,TRUE\nHf4(CuNi)3,TRUE\nHf40.9Nb5Cu54.1,TRUE\nHf41Nb44Si15,TRUE\nHf42.6Nb1Cu56.4,TRUE\nHf42Nb43Si15,TRUE\nHf42NbCu57,TRUE\nHf43(Nb14Si5)3,TRUE\nHf44Nb41Si15,TRUE\nHf46(Nb13Si5)3,TRUE\nHf47Nb38Si15,TRUE\nHf48Nb37Si15,TRUE\nHf49(Nb12Si5)3,TRUE\nHf4Cu5Ni,TRUE\nHf4CuNi5,TRUE\nHf4Ta31Fe65,TRUE\nHf4TaFe5,TRUE\nHf4Zr13Si3,TRUE\nHf51Nb34Si15,TRUE\nHf51V34Si15,TRUE\nHf52(Nb11Si5)3,TRUE\nHf52(V11Si5)3,TRUE\nHf53Nb32Si15,TRUE\nHf53V32Si15,TRUE\nHf54Nb31Si15,TRUE\nHf54V31Si15,TRUE\nHf54Zr3Be43,TRUE\nHf56Nb29Si15,TRUE\nHf56V29Si15,TRUE\nHf57Nb28Si15,TRUE\nHf57V28Si15,TRUE\nHf58(Nb9Si5)3,TRUE\nHf58(V9Si5)3,TRUE\nHf59Nb26Si15,TRUE\nHf59V26Si15,TRUE\nHf5Cu2Ni3,TRUE\nHf5Cu3Ni2,TRUE\nHf5Cu4Ni,TRUE\nHf5CuNi4,TRUE\nHf5Zr52Be43,TRUE\nHf61(Nb8Si5)3,TRUE\nHf61(V8Si5)3,TRUE\nHf62Nb23Si15,TRUE\nHf62V23Si15,TRUE\nHf63Nb22Si15,TRUE\nHf63V22Si15,TRUE\nHf64(Nb7Si5)3,TRUE\nHf64(V7Si5)3,TRUE\nHf66Nb19Si15,TRUE\nHf66V19Si15,TRUE\nHf67(Co10P)3,TRUE\nHf67(Co8Si3)3,TRUE\nHf67(Nb6Si5)3,TRUE\nHf67(Ni9P2)3,TRUE\nHf67(V6Si5)3,TRUE\nHf67Co33,TRUE\nHf67Ni33,TRUE\nHf68Nb17Si15,TRUE\nHf68V17Si15,TRUE\nHf69Nb16Si15,TRUE\nHf69V16Si15,TRUE\nHf6Cu3Ni,TRUE\nHf6CuNi3,TRUE\nHf6Zr11Si3,TRUE\nHf7(Fe27B4)3,TRUE\nHf7(Fe29B2)3,TRUE\nHf7.6Zr68.4Fe24,TRUE\nHf71Nb14Si15,TRUE\nHf71V14Si15,TRUE\nHf72Nb13Si15,TRUE\nHf72V13Si15,TRUE\nHf73(Nb4Si5)3,TRUE\nHf73(V4Si5)3,TRUE\nHf74Nb11Si15,TRUE\nHf74V11Si15,TRUE\nHf76(Nb3Si5)3,TRUE\nHf76(V3Si5)3,TRUE\nHf77Nb8Si15,TRUE\nHf77V8Si15,TRUE\nHf78Nb7Si15,TRUE\nHf78V7Si15,TRUE\nHf79(Nb2Si5)3,TRUE\nHf79(V2Si5)3,TRUE\nHf7Cu2Ni,TRUE\nHf7Cu3,TRUE\nHf7CuNi2,TRUE\nHf7Fe77B16,TRUE\nHf7Fe85B8,TRUE\nHf7Fe89B4,TRUE\nHf7Fe91B2,TRUE\nHf7Ni3,TRUE\nHf8(Nb3Si)3,TRUE\nHf8(Zr3Si)3,TRUE\nHf81Nb4Si15,TRUE\nHf81V4Si15,TRUE\nHf82(NbSi5)3,TRUE\nHf82(VSi5)3,TRUE\nHf83Nb2Si15,TRUE\nHf83V2Si15,TRUE\nHf84NbSi15,TRUE\nHf84VSi15,TRUE\nHf8CuNi,FALSE\nHf9.5Fe48.9O41.6,FALSE\nHf9.8Fe87.9B2.3,TRUE\nHf9Cu6Ni5,TRUE\nHf9Cu7Ni4,TRUE\nHf9Cu8Ni3,TRUE\nHf9Nb8Si3,TRUE\nHfCu,TRUE\nHfCu2Ni7,FALSE\nHfCu3Ni,TRUE\nHfCu4Ni5,FALSE\nHfCu5Ni4,FALSE\nHfCu7Ni2,FALSE\nHfCuNi3,TRUE\nHfFe,TRUE\nHfNi,TRUE\nHfTa4Fe5,TRUE\nHo(Fe5B)4,TRUE\nHo2Fe19B4,TRUE\nHoFe41B8,TRUE\nLa(Al2Ni)3,FALSE\nLa(Al6Ni)7,TRUE\nLa(AlCu)2,FALSE\nLa(AlCu2)3,FALSE\nLa(AlNi)2,TRUE\nLa(AlNi2)3,FALSE\nLa(Mg2Cu)3,TRUE\nLa(Mg2Ni)3,TRUE\nLa(MgCu)2,TRUE\nLa(MgNi)2,TRUE\nLa0.3Zr10Fe89.7,TRUE\nLa10Al14Ni,TRUE\nLa10Al3Ni7,TRUE\nLa10Al7Cu3,TRUE\nLa10Al7Ni3,TRUE\nLa11(Al2Cu)3,TRUE\nLa11(Al2Ni)3,TRUE\nLa11(AlNi2)3,TRUE\nLa11Al2Ni7,TRUE\nLa11Al4Cu5,TRUE\nLa11Al4Ni5,TRUE\nLa11Al5Ag4,TRUE\nLa11Al5Au4,TRUE\nLa11Al5Co4,TRUE\nLa11Al5Cr4,TRUE\nLa11Al5Cu4,TRUE\nLa11Al5Fe4,TRUE\nLa11Al5Ni4,TRUE\nLa11Al5Pt4,TRUE\nLa11Al5Zn4,TRUE\nLa11Al7Cu2,TRUE\nLa11Al7Ni2,TRUE\nLa11Al8Ni,TRUE\nLa11AlNi8,TRUE\nLa11Cu44.5Au44.5,TRUE\nLa11Mn4Al5,TRUE\nLa12Al3Cu5,TRUE\nLa12Al3Ni5,TRUE\nLa12Al5Cu3,TRUE\nLa12Al5Ni3,TRUE\nLa12Al7Ni,TRUE\nLa12Mg5Ni8,TRUE\nLa12Ni13,TRUE\nLa13(Al25Ni4)3,TRUE\nLa13(Al27Ni2)3,TRUE\nLa13Al2Ni5,TRUE\nLa13Al3Ni4,TRUE\nLa13Al4Ni3,TRUE\nLa13Al5Cu2,TRUE\nLa13Al5Ni2,TRUE\nLa13Al6Ni,TRUE\nLa13Al71Ni16,TRUE\nLa13Al73Ni14,TRUE\nLa13Al77Ni10,TRUE\nLa13Al79Ni8,TRUE\nLa13Al83Ni4,TRUE\nLa13Al85Ni2,TRUE\nLa13AlNi6,TRUE\nLa14(AlNi)3,TRUE\nLa14Al5Ni,TRUE\nLa14Al69Ni17,TRUE\nLa15Al2Ni3,TRUE\nLa15Al3Ni2,TRUE\nLa15Al3Ni32,TRUE\nLa15Al4Ni,TRUE\nLa15AlNi4,TRUE\nLa16Al3Ni,TRUE\nLa16Al3Ni31,TRUE\nLa16Al67Ni17,TRUE\nLa17AlNi2,TRUE\nLa18Al65Ni17,TRUE\nLa2(Al5Ni)3,TRUE\nLa2(CuAu)9,TRUE\nLa2(Mg5Cu)3,FALSE\nLa2(Mg5Ni)3,TRUE\nLa20Al21Ni59,TRUE\nLa20Al63Ni17,TRUE\nLa20AlNi29,TRUE\nLa21Al28Ni,TRUE\nLa21AlNi28,TRUE\nLa22Al19Ni59,TRUE\nLa22Al61Ni17,TRUE\nLa22AlNi27,TRUE\nLa24Al17Ni59,TRUE\nLa24Al59Ni17,TRUE\nLa26Al15Ni59,TRUE\nLa26Al57Ni17,TRUE\nLa27Al11Ni62,TRUE\nLa27Al9Ni64,TRUE\nLa28Al55Ni17,TRUE\nLa2Al16Ni7,TRUE\nLa2Al17Cu,TRUE\nLa2Al17Ni,TRUE\nLa2Al23,TRUE\nLa2Al2Cu,FALSE\nLa2Al2Ni,TRUE\nLa2Al3,FALSE\nLa2Al3Cu5,FALSE\nLa2Al3Ni5,TRUE\nLa2Al5Cu3,FALSE\nLa2Al5Ni3,TRUE\nLa2Al7Ni,FALSE\nLa2AlCu,TRUE\nLa2AlCu2,TRUE\nLa2AlCu7,FALSE\nLa2AlNi,TRUE\nLa2AlNi2,TRUE\nLa2AlNi7,FALSE\nLa2Mg13Ni5,TRUE\nLa2Mg13Zn5,TRUE\nLa2Mg17Ni,FALSE\nLa2Mg18Zn5,TRUE\nLa2Mg2Cu,TRUE\nLa2Mg2Ni,FALSE\nLa2Mg37Zn11,TRUE\nLa2Mg3Cu5,TRUE\nLa2Mg5Cu3,TRUE\nLa2Mg5Ni3,TRUE\nLa2Mg7Ni,TRUE\nLa2MgCu2,FALSE\nLa2Ni3,FALSE\nLa3(Mg10Ni)2,TRUE\nLa30Al53Ni17,TRUE\nLa32Al53Ni15,TRUE\nLa34Al53Ni13,TRUE\nLa36Al53Ni11,TRUE\nLa37(Al19Ni2)3,TRUE\nLa37Al53Ni10,TRUE\nLa37Al55Ni8,TRUE\nLa39Al2Ni59,TRUE\nLa3Al10Ni7,FALSE\nLa3Al13Ni4,TRUE\nLa3Al14Ni3,FALSE\nLa3Al15Ni2,FALSE\nLa3Al15Ni7,TRUE\nLa3Al16Ni,FALSE\nLa3Al2,TRUE\nLa3Al2Cu5,TRUE\nLa3Al2Ni5,TRUE\nLa3Al33Ni14,TRUE\nLa3Al3Cu4,TRUE\nLa3Al3Ni4,TRUE\nLa3Al44Ni3,TRUE\nLa3Al4Cu3,FALSE\nLa3Al4Ni3,TRUE\nLa3Al5Cu2,FALSE\nLa3Al5Ni2,TRUE\nLa3Al6Ni,FALSE\nLa3Al6Ni11,FALSE\nLa3Al7,FALSE\nLa3Al8Ni9,FALSE\nLa3AlCu,TRUE\nLa3AlCu6,FALSE\nLa3AlNi,TRUE\nLa3AlNi6,TRUE\nLa3Cu2,FALSE\nLa3Fe81B16,TRUE\nLa3Mg10Ni7,TRUE\nLa3Mg11Ni6,TRUE\nLa3Mg12Ni5,TRUE\nLa3Mg13Ni4,TRUE\nLa3Mg14Cu3,FALSE\nLa3Mg14Ni3,TRUE\nLa3Mg15Ni2,TRUE\nLa3Mg16Ni,FALSE\nLa3Mg2Cu5,FALSE\nLa3Mg3Cu4,TRUE\nLa3Mg3Ni4,TRUE\nLa3Mg4Cu3,TRUE\nLa3Mg4Ni3,TRUE\nLa3Mg5Cu2,TRUE\nLa3Mg5Ni2,TRUE\nLa3Mg6Ni,FALSE\nLa3Mg72Zn25,TRUE\nLa3Mg75Zn22,TRUE\nLa3Ni2,TRUE\nLa3Ni7,FALSE\nLa3Zr5Fe42,TRUE\nLa4(Al2Ni)7,TRUE\nLa4(AlNi)3,TRUE\nLa4(MgCu)3,TRUE\nLa41AlNi8,TRUE\nLa43Al3Ni4,TRUE\nLa43Al4Ni3,TRUE\nLa43Al57,TRUE\nLa43Al5Ni2,TRUE\nLa49AlNi50,TRUE\nLa4Al,TRUE\nLa4Al11Ni5,TRUE\nLa4Al45Ni,TRUE\nLa4Al5Cu,FALSE\nLa4Al5Ni,TRUE\nLa4Al5Ni11,TRUE\nLa4AlCu5,FALSE\nLa4AlNi5,TRUE\nLa4Cu,FALSE\nLa4Mg11Cu5,TRUE\nLa4Mg11Ni5,TRUE\nLa4Mg13Ni3,TRUE\nLa4Mg5Cu,FALSE\nLa4Mg5Ni,TRUE\nLa4Mg7Ni9,TRUE\nLa4Mg9Ni7,TRUE\nLa4MgNi5,FALSE\nLa4Ni,TRUE\nLa5(Al14Ni)3,TRUE\nLa5(Al2Ni3)3,TRUE\nLa5(Al3Ni2)3,TRUE\nLa5(AlNi4)3,FALSE\nLa5(Mg3Ni2)3,TRUE\nLa5Al13Ni2,FALSE\nLa5Al14Ni,FALSE\nLa5Al2Ni13,FALSE\nLa5Al2Ni3,TRUE\nLa5Al31Ni14,TRUE\nLa5Al3Cu2,TRUE\nLa5Al3Ni2,TRUE\nLa5Al44Ni,TRUE\nLa5Al4Cu,FALSE\nLa5Al4Ni,TRUE\nLa5Al7Ni8,TRUE\nLa5Al87Ni8,TRUE\nLa5Al8Ni7,TRUE\nLa5Al91Ni4,TRUE\nLa5AlNi4,TRUE\nLa5Mg11Cu4,FALSE\nLa5Mg2Cu3,FALSE\nLa5Mg2Ni3,FALSE\nLa5Mg3Cu2,FALSE\nLa6(AlNi)7,TRUE\nLa62.5Cu37.5,TRUE\nLa63Cu37,TRUE\nLa6Al11Ni3,FALSE\nLa6Al13Ni,FALSE\nLa6Al3Cu,TRUE\nLa6Al3Ni,TRUE\nLa6Al3Ni11,TRUE\nLa6Al5Ni9,TRUE\nLa6Al85Ni9,TRUE\nLa6Al9Ni5,TRUE\nLa6AlCu3,TRUE\nLa6AlNi3,TRUE\nLa6Mg11Cu3,FALSE\nLa6Mg15Ni4,TRUE\nLa6Mg9Cu5,TRUE\nLa6Mg9Ni5,TRUE\nLa7.5Al85Mo7.5,TRUE\nLa7.5Nb7.5Al85,TRUE\nLa7.5Zr7.5Al85,TRUE\nLa73Cu27,TRUE\nLa7Al10Ni3,TRUE\nLa7Al11Ni2,FALSE\nLa7Al29Ni14,TRUE\nLa7Al2Cu,FALSE\nLa7Al2Ni,TRUE\nLa7Al2Ni11,TRUE\nLa7Al3,TRUE\nLa7Al43,TRUE\nLa7Al4Ni9,TRUE\nLa7Al6Cu7,TRUE\nLa7Al6Ni7,TRUE\nLa7Al7Ni6,TRUE\nLa7Al88Ni5,TRUE\nLa7Al89Ni4,TRUE\nLa7Al8Ni5,TRUE\nLa7Al91Ni2,TRUE\nLa7Al9Ni4,TRUE\nLa7AlCu2,FALSE\nLa7AlNi2,TRUE\nLa7Mg10Ni3,TRUE\nLa7Mg71Zn22,TRUE\nLa7Ni3,TRUE\nLa8(Al3Ni)3,TRUE\nLa8(Al9Ni5)3,TRUE\nLa8(AlNi3)3,TRUE\nLa8(Mg3Cu)3,TRUE\nLa81AlNi18,TRUE\nLa83Al3Ni14,TRUE\nLa83Al5Ni12,TRUE\nLa87Al11Ni2,TRUE\nLa87Al13,TRUE\nLa8Al11Ni,TRUE\nLa8Al5Cu7,TRUE\nLa8Al5Ni7,TRUE\nLa8Al7Ni5,TRUE\nLa8AlCu,FALSE\nLa8AlNi,TRUE\nLa8AlNi11,TRUE\nLa8Mg67Zn25,TRUE\nLa8Mg7Cu5,TRUE\nLa9(Mg5Ni3)2,TRUE\nLa9Al,FALSE\nLa9Al10Ni,TRUE\nLa9Al11,TRUE\nLa9Al12Ni29,TRUE\nLa9Al13Ni28,TRUE\nLa9Al14Ni27,TRUE\nLa9Al15Ni26,TRUE\nLa9Al16Ni25,TRUE\nLa9Al17Ni24,TRUE\nLa9Al18Ni23,TRUE\nLa9Al19Ni22,TRUE\nLa9Al20Ni21,TRUE\nLa9Al21Ni20,TRUE\nLa9Al22Ni19,TRUE\nLa9Al23Ni18,TRUE\nLa9Al24Ni17,TRUE\nLa9Al25Ni16,TRUE\nLa9Al2Ni9,TRUE\nLa9Al4Ni7,TRUE\nLa9Al5Ni6,TRUE\nLa9Al6Ni5,TRUE\nLa9Al7Ni4,TRUE\nLa9Al8Ni3,TRUE\nLa9Al9Ni2,TRUE\nLa9AlNi15,TRUE\nLa9Cu36.4Au54.6,TRUE\nLa9Cu45.5Au45.5,TRUE\nLa9Cu68.25Au22.75,TRUE\nLa9Mg35Ni6,TRUE\nLa9Mg85Ni6,TRUE\nLa9Ni,FALSE\nLaAl,TRUE\nLaAl14Ni5,TRUE\nLaAl15Ni4,TRUE\nLaAl17Cu2,FALSE\nLaAl17Ni2,TRUE\nLaAl17Ni7,TRUE\nLaAl18Cu,TRUE\nLaAl18Ni,FALSE\nLaAl2Ni,TRUE\nLaAl2Ni7,FALSE\nLaAl36Ni13,TRUE\nLaAl37Ni12,TRUE\nLaAl38Ni11,TRUE\nLaAl39Ni10,TRUE\nLaAl3Ni,TRUE\nLaAl4,FALSE\nLaAl40Ni9,TRUE\nLaAl41Ni8,TRUE\nLaAl43Ni6,TRUE\nLaAl44Ni5,TRUE\nLaAl4Ni5,FALSE\nLaAl5Cu4,FALSE\nLaAl5Ni4,FALSE\nLaAl7Cu2,FALSE\nLaAl8Cu,FALSE\nLaAl8Ni,TRUE\nLaAl9,TRUE\nLaAlCu3,FALSE\nLaAlCu8,FALSE\nLaAlNi3,FALSE\nLaAlNi8,FALSE\nLaCu,FALSE\nLaMg11Cu8,TRUE\nLaMg13Cu6,TRUE\nLaMg14Zn5,TRUE\nLaMg15Cu4,TRUE\nLaMg15Ni4,TRUE\nLaMg15Zn4,TRUE\nLaMg16Cu3,TRUE\nLaMg16Ni3,TRUE\nLaMg17Ni2,TRUE\nLaMg18Ni,FALSE\nLaMg19Zn5,TRUE\nLaMg2Cu,FALSE\nLaMg2Ni,TRUE\nLaMg3Cu,FALSE\nLaMg3Ni,TRUE\nLaMg4Cu5,TRUE\nLaMg5Cu4,TRUE\nLaMg5Ni4,TRUE\nLaMg7Cu2,TRUE\nLaMg7Ni2,TRUE\nLaMg7Zn2,TRUE\nLaMg8Cu,FALSE\nLaMg8Ni,TRUE\nLaNi,FALSE\nLaZr5Fe44,TRUE\nMg,FALSE\nMg10AlZn9,TRUE\nMg10Ti53Al37,TRUE\nMg11(Al8Pd5)3,FALSE\nMg11Al2Ag7,TRUE\nMg11Al4Ag5,TRUE\nMg11Ti14Al25,FALSE\nMg11Ti25Al14,TRUE\nMg11Ti29Al60,TRUE\nMg11Ti32Al57,TRUE\nMg11Zn9,FALSE\nMg12AlZn7,TRUE\nMg12Ti7Al,FALSE\nMg13(Ti18Al11)3,TRUE\nMg13(Ti2Al)29,TRUE\nMg13(Ti9Al20)3,FALSE\nMg13Al2Ag5,TRUE\nMg13Al2Zn5,TRUE\nMg13AlZn6,TRUE\nMg13Ti12,FALSE\nMg13Ti19Al68,FALSE\nMg13Zn7,TRUE\nMg14(AlZn)3,FALSE\nMg14AlZn5,TRUE\nMg15Al2Ag3,TRUE\nMg15Al2Zn3,TRUE\nMg15Al3Zn2,FALSE\nMg15AlZn4,TRUE\nMg15Ti32Al53,TRUE\nMg15Ti49Al36,FALSE\nMg16Al27Pd7,FALSE\nMg16Al3Zn,FALSE\nMg16AlZn3,FALSE\nMg17Al2Zn,FALSE\nMg17Al52Pd31,FALSE\nMg17Al71Pd12,TRUE\nMg17AlZn2,FALSE\nMg17Cu3,FALSE\nMg17Mn3,FALSE\nMg17Ni3,TRUE\nMg17Ti36Al47,FALSE\nMg17Ti60Al23,FALSE\nMg17Zn3,FALSE\nMg18Al25Pd7,FALSE\nMg18AlZn,FALSE\nMg18Ti27Al55,FALSE\nMg19(AlGa)3,TRUE\nMg19(AlGa2)2,TRUE\nMg19Mn,FALSE\nMg19Zn,FALSE\nMg20Al23Pd7,FALSE\nMg20Ti43Al37,FALSE\nMg21Al53Pd26,TRUE\nMg22(Al3Pd)7,FALSE\nMg22Ti67Al11,FALSE\nMg23(AlGa2)9,TRUE\nMg23(Ti2Al5)11,FALSE\nMg23Ti20Al7,FALSE\nMg23Ti61Al16,FALSE\nMg27Ti43Al30,FALSE\nMg27Ti45Al28,TRUE\nMg27Ti52Al21,FALSE\nMg2Al2Zn,FALSE\nMg2AlZn2,FALSE\nMg2Ti53Al45,TRUE\nMg3(Ti6Al5)2,TRUE\nMg30Ti43Al27,FALSE\nMg31(Ti18Al5)3,FALSE\nMg33Al67,FALSE\nMg33Ti14Al3,FALSE\nMg35(Zn4In)3,TRUE\nMg35(Zn4Sn)3,TRUE\nMg39Ti41Al20,FALSE\nMg3Al11Pd6,FALSE\nMg3Al17,FALSE\nMg3AlZn,FALSE\nMg3Cu2,TRUE\nMg3Ti20Al77,FALSE\nMg3Ti27Al70,FALSE\nMg3Ti34Al63,TRUE\nMg3Ti5Al17,TRUE\nMg3Ti7Al10,TRUE\nMg3Ti7Al15,TRUE\nMg3Zn,TRUE\nMg3Zn2,TRUE\nMg4(AlZn)3,FALSE\nMg41Ti50Al9,FALSE\nMg44Al43Pd13,FALSE\nMg45Al4Ga,FALSE\nMg46Ti35Al19,FALSE\nMg4Al5Zn,FALSE\nMg4AlZn5,FALSE\nMg4Cu,TRUE\nMg4Ni,TRUE\nMg4Zn,FALSE\nMg51Ti40Al9,FALSE\nMg5Al2Zn3,FALSE\nMg5Al3Zn2,FALSE\nMg5Al4Zn,FALSE\nMg5Al74Pd21,FALSE\nMg5AlZn4,FALSE\nMg5Ti19Al26,TRUE\nMg5Ti29Al66,TRUE\nMg6(CuAg)7,TRUE\nMg6Al3Zn,FALSE\nMg6AlZn3,FALSE\nMg6Ti61Al33,TRUE\nMg7(Ti12Al19)3,TRUE\nMg7(Ti18Al13)3,TRUE\nMg7(Ti2Al)6,FALSE\nMg70(Cu7Au3)3,TRUE\nMg70(Cu9Au)3,TRUE\nMg70Cu29Au,TRUE\nMg77Ti23,FALSE\nMg7Al2Zn,FALSE\nMg7Al4Ag9,TRUE\nMg7AlZn2,TRUE\nMg7Cu3,TRUE\nMg7Ni3,FALSE\nMg7Ti49Al44,TRUE\nMg7Zn3,TRUE\nMg83Ti17,FALSE\nMg89Al8Ga3,FALSE\nMg89Al9Ga2,FALSE\nMg8AlZn,FALSE\nMg92.5Mn7.5,FALSE\nMg9Al26Pd15,FALSE\nMg9Al4Ag7,TRUE\nMg9Cu,FALSE\nMg9Mn,FALSE\nMg9Ni,TRUE\nMg9Ti11Al5,FALSE\nMg9Ti21Al20,TRUE\nMg9Ti28Al13,TRUE\nMg9Ti44Al47,TRUE\nMg9Zn,FALSE\nMgAl2Pd,FALSE\nMgCu,FALSE\nMn(Al11Co)2,FALSE\nMn(Al11Ni)2,FALSE\nMn(Al29Ni4)3,TRUE\nMn(Al2Ge)3,TRUE\nMn(Al2Si)3,TRUE\nMn(Al6Co)7,FALSE\nMn(Al6Ni)7,FALSE\nMn(Al7Co)3,FALSE\nMn(Al7Ni)3,FALSE\nMn(Al8Ni)11,TRUE\nMn(Fe29B4)3,FALSE\nMn(Fe31B2)3,FALSE\nMn(Ge2Pd9)9,TRUE\nMn0.5Al87.5Ni12,TRUE\nMn10(Co4B)3,TRUE\nMn10Al73Ge17,TRUE\nMn10Co8B7,TRUE\nMn11(Co9B4)3,TRUE\nMn11Co11B3,TRUE\nMn11Co25B14,TRUE\nMn12Co7B6,TRUE\nMn12Co8B5,TRUE\nMn12Fe71P17,TRUE\nMn12Nb15Co73,TRUE\nMn13(CoB)6,TRUE\nMn13.4Co53.6B33,TRUE\nMn13.5Co54.5B32,TRUE\nMn13.6Co54.4B32,TRUE\nMn13Co31B6,TRUE\nMn14.4Co57.6B28,TRUE\nMn14FeB5,TRUE\nMn15(Fe4P)17,TRUE\nMn15.2Co60.8B24,TRUE\nMn15.5Al76Cu8.5,FALSE\nMn15Co61B24,TRUE\nMn15Fe71B14,TRUE\nMn15Fe73B12,FALSE\nMn15Fe77B8,FALSE\nMn15Fe79B6,FALSE\nMn16(Co2B)3,TRUE\nMn16.8Co67.2B16,TRUE\nMn16Co5B4,TRUE\nMn17(Co7B4)3,TRUE\nMn17.4Al66.6Si16,FALSE\nMn17.4Al68.6Si14,FALSE\nMn17.4Al70.6Si12,FALSE\nMn17.4Al72.5Si10.1,FALSE\nMn17.4Al74.6Si8,FALSE\nMn17.4Al76.6Si6,FALSE\nMn17.4Al78.6Si4,FALSE\nMn17.5Co70.5B12,TRUE\nMn17.6Co70.4B12,TRUE\nMn17.8Co71.2B11,TRUE\nMn17Co25B8,TRUE\nMn17Co67B16,TRUE\nMn17Fe5B3,FALSE\nMn18.5Co65.5B16,TRUE\nMn18Al57Ge25,TRUE\nMn18Fe5B2,FALSE\nMn19(Nb5Co22)3,TRUE\nMn19Co19B12,TRUE\nMn19Co65B16,TRUE\nMn1Al86.5Ni12.5,TRUE\nMn2(Al15Co)3,FALSE\nMn2(Al15Ni)3,FALSE\nMn2(NbCo5)3,TRUE\nMn2.5Al87Ni10.5,TRUE\nMn2.5Fe80.5B17,TRUE\nMn20Al53Si27,TRUE\nMn21.6Co46.4B32,TRUE\nMn21.6Co50.4B28,TRUE\nMn21Co15B14,TRUE\nMn21Co17B12,TRUE\nMn21Co21B8,TRUE\nMn21Co47B32,TRUE\nMn21Co51B28,TRUE\nMn22.8Co53.2B24,TRUE\nMn23Co53B24,TRUE\nMn23Co57B20,TRUE\nMn25.2Co58.8B16,TRUE\nMn25Co47B28,TRUE\nMn25Co59B16,TRUE\nMn26.4Co61.6B12,TRUE\nMn26.5Co45.5B28,TRUE\nMn26.5Co49.5B24,TRUE\nMn26.6Co49.4B24,TRUE\nMn26.8Co40.2B33,TRUE\nMn27Co17B6,TRUE\nMn27Co41B32,TRUE\nMn27Co45B28,TRUE\nMn27Co61B12,TRUE\nMn28.8Co43.2B28,TRUE\nMn28Co41B31,TRUE\nMn29.5Co46.5B24,TRUE\nMn29.5Co54.5B16,TRUE\nMn29Co43B28,TRUE\nMn2Al11Si7,TRUE\nMn2Al13Si5,TRUE\nMn2Al20Ni3,FALSE\nMn2Al21Ni2,FALSE\nMn2Al22Ni,FALSE\nMn2Al23,FALSE\nMn2Al41Ni7,FALSE\nMn2Al43Co5,FALSE\nMn2Al43Ni5,FALSE\nMn2Al47Co,FALSE\nMn2Al47Ni,FALSE\nMn2Al5Si3,TRUE\nMn2Al85Ni13,FALSE\nMn2Al86.5Ni11.5,TRUE\nMn2Al87Ni11,TRUE\nMn2Al89Ni9,FALSE\nMn2Co17B6,TRUE\nMn2Co18B5,TRUE\nMn2Co19B4,TRUE\nMn2Co2B,TRUE\nMn2Fe18B5,TRUE\nMn2Nb15Co83,TRUE\nMn30.4Co45.6B24,TRUE\nMn30.5Co41.5B28,TRUE\nMn30.5Co45.5B24,TRUE\nMn31(Co19B4)3,TRUE\nMn31Co41B28,TRUE\nMn32.5Co47.5B20,TRUE\nMn33.5Co50.5B16,TRUE\nMn33.6Co50.4B16,TRUE\nMn33Fe10B7,TRUE\nMn35(Co3B2)3,TRUE\nMn35.2Co52.8B12,TRUE\nMn35.6Co53.4B11,TRUE\nMn35Co37B28,TRUE\nMn35Co49B16,TRUE\nMn35Co53B12,TRUE\nMn37(Co13B8)3,TRUE\nMn38.5Co41.5B20,TRUE\nMn39Co49B12,TRUE\nMn3Al10Si7,TRUE\nMn3Al11Si6,TRUE\nMn3Al12Si5,TRUE\nMn3Al13Cu4,FALSE\nMn3Al13Si4,TRUE\nMn3Al16Ni,FALSE\nMn3Al40Ni7,FALSE\nMn3Al41Ni6,FALSE\nMn3Al42Ni5,FALSE\nMn3Al43Co4,FALSE\nMn3Al43Ni4,FALSE\nMn3Al44Co3,FALSE\nMn3Al44Ni3,FALSE\nMn3Al45Co2,FALSE\nMn3Al45Ni2,FALSE\nMn3Al46Co,FALSE\nMn3Al46Ni,FALSE\nMn3Al47,FALSE\nMn3Al9Si8,FALSE\nMn3CoB,TRUE\nMn3Fe15B2,FALSE\nMn3Fe37B10,TRUE\nMn3Fe81B16,TRUE\nMn3Fe83B14,TRUE\nMn3Fe85B12,FALSE\nMn3Fe87B10,FALSE\nMn3Fe89B8,FALSE\nMn3Fe91B6,FALSE\nMn3Fe93B4,FALSE\nMn3Si10Pd37,TRUE\nMn3Si20Pd77,TRUE\nMn4(Nb5Co27)3,TRUE\nMn40.5Co43.5B16,TRUE\nMn43(Co11B8)3,TRUE\nMn43(Co15B4)3,TRUE\nMn43.5Co36.5B20,TRUE\nMn43Co37B20,TRUE\nMn47Co25B28,TRUE\nMn49(Co13B4)3,TRUE\nMn49(Co9B8)3,TRUE\nMn49Co35B16,TRUE\nMn4Al11Si5,TRUE\nMn4Al13Ge3,FALSE\nMn4Al13Si3,FALSE\nMn4Al41Ni5,FALSE\nMn4Al43Ni3,FALSE\nMn4Al45Co,FALSE\nMn4Al45Ni,FALSE\nMn4Al83Ni13,FALSE\nMn4Al9Si7,TRUE\nMn4Co16B5,TRUE\nMn4Fe16B5,TRUE\nMn4Fe77B19,TRUE\nMn5(Al7Ge8)3,TRUE\nMn5(Co3B2)4,TRUE\nMn5(Fe13B2)3,FALSE\nMn5(Fe14B)3,FALSE\nMn51.5Co28.5B20,TRUE\nMn51Co33B16,TRUE\nMn57Co27B16,TRUE\nMn59.5Co24.5B16,TRUE\nMn59Co25B16,TRUE\nMn5Al8Si7,FALSE\nMn5Co13B7,TRUE\nMn5Co17B3,TRUE\nMn5Fe37B8,TRUE\nMn5Fe38B7,TRUE\nMn5Fe41B4,FALSE\nMn5Fe81B14,TRUE\nMn5Fe83B12,FALSE\nMn5Fe87B8,FALSE\nMn5Fe89B6,FALSE\nMn5Fe91B4,FALSE\nMn5Ge18Pd77,TRUE\nMn63Co21B16,TRUE\nMn67Co17B16,TRUE\nMn6Al69Ge25,TRUE\nMn6Co11B8,TRUE\nMn6Co13B6,TRUE\nMn6Co14B5,TRUE\nMn6Nb15Co79,TRUE\nMn7(Co2B)6,TRUE\nMn7(Ge6Pd25)3,TRUE\nMn7.2Co64.8B28,TRUE\nMn7.5Co67.5B25,TRUE\nMn7.6Co68.4B24,TRUE\nMn74(SiP)13,TRUE\nMn74Si23P3,TRUE\nMn7Al33Si10,TRUE\nMn7Al85Ni8,FALSE\nMn7Co13B5,TRUE\nMn7Co27B16,TRUE\nMn7Co29B14,TRUE\nMn7Co61B32,TRUE\nMn7Co65B28,TRUE\nMn7Fe2B,FALSE\nMn7Fe33B10,TRUE\nMn7Si20Pd73,TRUE\nMn8.4Co75.6B16,TRUE\nMn85(Fe2B3)3,TRUE\nMn8Co12B5,TRUE\nMn8Nb15Co77,TRUE\nMn9Co11B5,TRUE\nMn9Co35B6,TRUE\nMn9Co75B16,TRUE\nMn9Co79B12,TRUE\nMn9Co9B7,TRUE\nMn9Fe31B10,TRUE\nMn9Fe74P17,TRUE\nMnAl12Si7,FALSE\nMnAl14Si5,FALSE\nMnAl23Co,FALSE\nMnAl23Ni,FALSE\nMnAl24,FALSE\nMnAl2Si,FALSE\nMnAl3Si,FALSE\nMnAl43Co6,FALSE\nMnAl44Co5,FALSE\nMnAl44Ni5,TRUE\nMnAl45Co4,FALSE\nMnAl45Ni4,FALSE\nMnAl46Co3,FALSE\nMnAl46Ni3,FALSE\nMnAl47Co2,FALSE\nMnAl47Ni2,FALSE\nMnAl48Co,FALSE\nMnAl48Ni,FALSE\nMnAl49,FALSE\nMnAl5Ge4,TRUE\nMnAlCu2,FALSE\nMnCo3B,TRUE\nMnFe15B4,TRUE\nMnFe17B2,FALSE\nMnFe19B5,TRUE\nMnFe39B10,TRUE\nMnFe3B,TRUE\nMnFe7B2,TRUE\nMnFe83B16,TRUE\nMnFe85B14,TRUE\nMnFe89B10,FALSE\nMnFe8B,FALSE\nMnFe91B8,FALSE\nMnFe95B4,FALSE\nMnGe9Pd40,TRUE\nMnSi10Pd39,TRUE\nMnSi20Pd79,TRUE\nMnSi4Pd15,TRUE\nMnSi5Pd19,TRUE\nMo12P5Rh8,TRUE\nMo12P5Ru8,TRUE\nMo16P5Ru4,TRUE\nMo3Ru2,TRUE\nMo4P5Ru16,TRUE\nMo8P5Ru12,TRUE\nNb10.3Fe80.3B9.4,TRUE\nNb10Ni73B17,TRUE\nNb11.5Ni71.5B17,TRUE\nNb11Si4Mo5,TRUE\nNb11V5Si4,FALSE\nNb12Fe83B5,FALSE\nNb12Fe85B3,FALSE\nNb13Co77B10,TRUE\nNb13Si4Mo3,TRUE\nNb13Si4W3,FALSE\nNb13V3Si4,TRUE\nNb14Co81B5,TRUE\nNb15Co73Ni12,TRUE\nNb15Fe12Co73,TRUE\nNb15Fe26Co59,TRUE\nNb15Fe2Co83,TRUE\nNb15Fe3.5Co81.5,TRUE\nNb15Fe42.5Co42.5,TRUE\nNb15Fe4Co81,TRUE\nNb15Fe6Co79,TRUE\nNb15Fe72.5Co12.5,TRUE\nNb15Fe77B8,TRUE\nNb15Fe79B6,FALSE\nNb15Si2Ge3,TRUE\nNb15Si4Mo,TRUE\nNb15Si4W,TRUE\nNb15VSi4,TRUE\nNb16.5Ni66.5B17,TRUE\nNb17Si3,TRUE\nNb19(Si2Ge)2,TRUE\nNb19Si5Ge,TRUE\nNb20Si3C2,TRUE\nNb20Si4C,TRUE\nNb20Si4Ge,TRUE\nNb2Co20B3,TRUE\nNb2Ni3,TRUE\nNb3(Fe10B)2,TRUE\nNb39Si7Ge4,TRUE\nNb3Co17,TRUE\nNb3Fe12Co5,TRUE\nNb3Fe15B2,TRUE\nNb3Fe16B,FALSE\nNb3Fe2Co15,TRUE\nNb3Fe80B17,TRUE\nNb3Ni2,TRUE\nNb3SiMo,TRUE\nNb3VSi,TRUE\nNb40(Ni19Pt)3,TRUE\nNb40Ni59Ir,TRUE\nNb40Ni59Pd,TRUE\nNb40Ni59Pt,TRUE\nNb40Si7C3,TRUE\nNb40Si9C,TRUE\nNb40Si9Ge,TRUE\nNb4Si,TRUE\nNb5(Co14B)3,FALSE\nNb5.3Fe80.2B14.5,TRUE\nNb5.5Fe81.5B13,FALSE\nNb5.5Fe85.5B9,FALSE\nNb5Fe83B12,TRUE\nNb5Fe87B8,FALSE\nNb5Fe89B6,FALSE\nNb5Fe92B3,FALSE\nNb5Ni78B17,TRUE\nNb5Si2Mo3,TRUE\nNb6.8Fe76B17.2,TRUE\nNb6.9Fe80B13.1,TRUE\nNb6Fe39B5,TRUE\nNb6Fe41B3,TRUE\nNb7(Fe27B4)3,TRUE\nNb7(Fe28B3)3,TRUE\nNb7.1Fe77.9B15,TRUE\nNb7.1Fe82.3B10.6,FALSE\nNb7.1Fe83.4B9.5,FALSE\nNb7.3Fe77.5B15.2,TRUE\nNb7.3Fe79.5B13.2,TRUE\nNb7.5Fe83B9.5,FALSE\nNb7.6Fe81.1B11.3,TRUE\nNb7.7Fe78.1B14.2,TRUE\nNb7.8Fe78.4B13.8,TRUE\nNb76.5Si8.5Ge15,TRUE\nNb77Si10Ge13,TRUE\nNb77Si23,TRUE\nNb7Co40B3,TRUE\nNb7Co42B,TRUE\nNb7Fe77B16,TRUE\nNb7Fe78.7B14.3,TRUE\nNb7Fe79.9B13.1,TRUE\nNb7Fe83B10,TRUE\nNb7Fe85B8,TRUE\nNb7Si2Mo,TRUE\nNb7Si2W,TRUE\nNb7VSi2,TRUE\nNb8.3Fe77.5B14.2,TRUE\nNb8.3Fe78.5B13.2,TRUE\nNb8.7Fe76B15.3,TRUE\nNb8.9Fe79.6B11.5,TRUE\nNb80Si17Ge3,TRUE\nNb80Si19C,TRUE\nNb80Si19Ge,TRUE\nNb8Fe75B17,TRUE\nNb8Fe79B13,TRUE\nNb8Ni75B17,TRUE\nNb9.1Fe79.9B11,TRUE\nNb9.3Fe77.5B13.2,TRUE\nNb9.6Fe77.5B12.9,TRUE\nNb9.6Fe77B13.4,TRUE\nNb9.8Fe75.2B15,TRUE\nNb9Si4Mo7,FALSE\nNbFe17B2,TRUE\nNbNi,TRUE\nNd(Al10Ni)9,FALSE\nNd(Al11Ni)2,TRUE\nNd(Al28Ni5)3,TRUE\nNd(Al5Ni)4,TRUE\nNd(Al6Ni)7,TRUE\nNd(Al7Ni)3,TRUE\nNd(Al8Ni)11,TRUE\nNd(AlCu11)2,FALSE\nNd(AlCu7)3,FALSE\nNd(Mg2Cu)3,TRUE\nNd(Mg2Ni)3,TRUE\nNd(MgCu)2,TRUE\nNd(MgCu2)3,FALSE\nNd(MgNi)2,TRUE\nNd10Al79Ni11,TRUE\nNd10Fe82.5B7.5,TRUE\nNd11.8Fe82.1B6.1,TRUE\nNd11Al5Ni4,TRUE\nNd11Fe89,TRUE\nNd12.375Fe70.125B17.5,TRUE\nNd12Fe69.5B18.5,TRUE\nNd13Fe79B8,TRUE\nNd14Fe78.2B7.8,TRUE\nNd14Fe81B5,FALSE\nNd14Fe82.2B4.8,TRUE\nNd15Fe77.5B7.5,TRUE\nNd15Fe77B8,TRUE\nNd15Fe82B3,TRUE\nNd16.5Fe66B17.5,TRUE\nNd16.8Fe67.2B16,TRUE\nNd2(Al15Ni)3,TRUE\nNd2(Al5Ni)3,TRUE\nNd2(Mg5Cu)3,TRUE\nNd2(Mg5Ni)3,TRUE\nNd2.5Mg97.5,FALSE\nNd20.625Fe61.875B17.5,TRUE\nNd20Fe61.5B18.5,TRUE\nNd21Fe21B8,TRUE\nNd21Fe79,TRUE\nNd27.7Fe56.3B16,TRUE\nNd2Al17Ni,TRUE\nNd2Al20Ni3,TRUE\nNd2Al21Ni2,TRUE\nNd2Al22Ni,TRUE\nNd2Al23,TRUE\nNd2Al2Cu21,TRUE\nNd2Al3Cu20,TRUE\nNd2Al41Ni7,TRUE\nNd2Al43Ni5,TRUE\nNd2Al47Ni,FALSE\nNd2Al5Cu43,FALSE\nNd2Al7Cu41,FALSE\nNd2Al7Ni,FALSE\nNd2Al85Ni13,TRUE\nNd2AlCu22,FALSE\nNd2Cu3,FALSE\nNd2Fe3,TRUE\nNd2Fe7B,TRUE\nNd2Mg11Cu7,TRUE\nNd2Mg11Ni7,TRUE\nNd2Mg13Cu5,TRUE\nNd2Mg13Ni5,TRUE\nNd2Mg17Cu,TRUE\nNd2Mg17Ni,TRUE\nNd2Mg2Cu,FALSE\nNd2Mg3Cu5,TRUE\nNd2Mg3Ni5,FALSE\nNd2Mg5Cu3,TRUE\nNd2Mg5Ni3,TRUE\nNd2Mg7Cu,TRUE\nNd2Mg7Ni,TRUE\nNd2MgCu2,FALSE\nNd2MgCu7,FALSE\nNd2MgNi2,TRUE\nNd2Ni3,FALSE\nNd3(Al10Ni)2,TRUE\nNd30Fe51.5B18.5,TRUE\nNd33.6Fe50.4B16,TRUE\nNd33Fe67,TRUE\nNd3Al13Ni4,TRUE\nNd3Al14Ni3,TRUE\nNd3Al15Ni2,TRUE\nNd3Al16Ni,FALSE\nNd3Al21Ni,TRUE\nNd3Al22,TRUE\nNd3Al2Cu45,FALSE\nNd3Al3Cu44,FALSE\nNd3Al41Ni6,TRUE\nNd3Al42Ni5,TRUE\nNd3Al43Ni4,TRUE\nNd3Al44Ni3,TRUE\nNd3Al45Ni2,TRUE\nNd3Al46Ni,FALSE\nNd3Al47,FALSE\nNd3Al4Cu43,FALSE\nNd3Al5Cu42,FALSE\nNd3Al6Cu41,FALSE\nNd3Al7Cu40,FALSE\nNd3Al90Ni7,TRUE\nNd3AlCu46,FALSE\nNd3Cu7,FALSE\nNd3Fe14B3,TRUE\nNd3Fe17,TRUE\nNd3Fe2,TRUE\nNd3Fe41B6,TRUE\nNd3Fe7,TRUE\nNd3Fe78.5B18.5,TRUE\nNd3Fe82B15,TRUE\nNd3Mg10Cu7,TRUE\nNd3Mg10Ni7,TRUE\nNd3Mg11Cu6,TRUE\nNd3Mg11Ni6,TRUE\nNd3Mg12Cu5,TRUE\nNd3Mg12Ni5,TRUE\nNd3Mg13Cu4,TRUE\nNd3Mg13Ni4,TRUE\nNd3Mg14Cu3,TRUE\nNd3Mg14Ni3,TRUE\nNd3Mg15Cu2,TRUE\nNd3Mg15Ni2,TRUE\nNd3Mg16Cu,FALSE\nNd3Mg16Ni,FALSE\nNd3Mg17,FALSE\nNd3Mg2Cu5,TRUE\nNd3Mg2Ni5,TRUE\nNd3Mg3Cu4,TRUE\nNd3Mg4Cu3,TRUE\nNd3Mg4Ni3,TRUE\nNd3Mg5Cu2,TRUE\nNd3Mg5Ni2,TRUE\nNd3Mg6Ni,TRUE\nNd3Mg9Ni8,TRUE\nNd3MgCu6,TRUE\nNd3MgNi,TRUE\nNd3MgNi6,FALSE\nNd3Ni2,TRUE\nNd3Ni7,FALSE\nNd4(MgNi)3,TRUE\nNd4.125Fe78.375B17.5,TRUE\nNd4.5Fe77B18.5,TRUE\nNd4Al13Ni3,FALSE\nNd4Al15Ni,FALSE\nNd4Al3Cu43,TRUE\nNd4Al41Ni5,TRUE\nNd4Al43Ni3,TRUE\nNd4Al45Ni,TRUE\nNd4Al5Cu41,TRUE\nNd4Al7Cu39,FALSE\nNd4AlCu45,FALSE\nNd4Fe19B2,TRUE\nNd4Fe77B19,TRUE\nNd4Mg11Cu5,TRUE\nNd4Mg11Ni5,TRUE\nNd4Mg13Cu3,TRUE\nNd4Mg13Ni3,TRUE\nNd4Mg15Ni,TRUE\nNd4Mg5Ni,FALSE\nNd4Mg9Cu7,TRUE\nNd4Mg9Ni7,TRUE\nNd4MgNi5,TRUE\nNd4Ni,FALSE\nNd5(Al14Ni)3,TRUE\nNd5(Al2Cu13)3,FALSE\nNd5(AlCu14)3,TRUE\nNd5(Mg3Cu2)3,TRUE\nNd5(Mg3Ni2)3,TRUE\nNd5(Mg4Cu)3,FALSE\nNd5(Mg4Ni)3,TRUE\nNd50.4Fe33.6B16,TRUE\nNd50Fe31.5B18.5,TRUE\nNd5Al2Cu43,FALSE\nNd5Al37Ni8,TRUE\nNd5Al41Ni4,TRUE\nNd5Al43Ni2,TRUE\nNd5Al44Ni,TRUE\nNd5Al4Cu41,FALSE\nNd5Al7Cu38,FALSE\nNd5Al87Ni8,TRUE\nNd5AlCu44,FALSE\nNd5Mg11Cu4,TRUE\nNd5Mg11Ni4,TRUE\nNd5Mg13Cu2,FALSE\nNd5Mg13Ni2,TRUE\nNd5Mg2Ni3,TRUE\nNd5Mg3Ni2,TRUE\nNd5Mg4Ni,FALSE\nNd5Mg7Ni8,TRUE\nNd5Mg83Ni12,TRUE\nNd5Mg88Ni7,TRUE\nNd5Mg8Ni7,TRUE\nNd5MgNi4,TRUE\nNd6Fe41B3,TRUE\nNd6Fe75.5B18.5,TRUE\nNd6Mg11Ni3,TRUE\nNd6Mg3Ni,FALSE\nNd6Mg9Cu5,TRUE\nNd6Mg9Ni5,TRUE\nNd6MgNi3,TRUE\nNd7(Al29Ni2)3,TRUE\nNd7.5Mg90Ni2.5,TRUE\nNd7.5Mg92.5,FALSE\nNd7Al43,TRUE\nNd7Al83Ni10,TRUE\nNd7Al85Ni8,TRUE\nNd7Fe13,TRUE\nNd7Mg10Ni3,TRUE\nNd7Mg11Ni2,TRUE\nNd7Mg2Ni,FALSE\nNd7Mg6Cu7,TRUE\nNd7Mg8Ni5,TRUE\nNd7Mg9Cu4,TRUE\nNd7Mg9Ni4,TRUE\nNd7MgNi2,FALSE\nNd7Ni3,TRUE\nNd8(Fe13B)3,FALSE\nNd8.25Fe74.25B17.5,TRUE\nNd9.2Fe74.8B16,TRUE\nNd9Al81Ni10,TRUE\nNd9Al83Ni8,TRUE\nNd9Al85Ni6,TRUE\nNd9Fe41,TRUE\nNd9Fe82B9,TRUE\nNdAl15Ni4,FALSE\nNdAl16Ni3,TRUE\nNdAl17Ni2,TRUE\nNdAl18Ni,TRUE\nNdAl23Ni,FALSE\nNdAl24,FALSE\nNdAl40Ni9,TRUE\nNdAl41Ni8,TRUE\nNdAl43Ni6,TRUE\nNdAl44Ni5,TRUE\nNdAl45Ni4,TRUE\nNdAl46Ni3,FALSE\nNdAl47Ni2,FALSE\nNdAl48Ni,FALSE\nNdAl49,FALSE\nNdAl5Cu44,FALSE\nNdAl7Ni2,TRUE\nNdAl86Ni13,TRUE\nNdAl8Ni,TRUE\nNdAl9,TRUE\nNdAlCu23,FALSE\nNdAlCu8,FALSE\nNdCu4,FALSE\nNdFe,TRUE\nNdFe3,TRUE\nNdFe4,TRUE\nNdFe9,TRUE\nNdMg11Cu8,TRUE\nNdMg13Cu6,TRUE\nNdMg13Ni6,TRUE\nNdMg14Cu5,TRUE\nNdMg15Cu4,TRUE\nNdMg15Ni4,TRUE\nNdMg16Cu3,TRUE\nNdMg17Cu2,TRUE\nNdMg17Ni2,TRUE\nNdMg18Cu,FALSE\nNdMg18Ni,FALSE\nNdMg19,FALSE\nNdMg2Cu,TRUE\nNdMg2Ni,TRUE\nNdMg3Cu,TRUE\nNdMg3Ni,TRUE\nNdMg4Cu5,TRUE\nNdMg5Cu4,TRUE\nNdMg5Ni4,FALSE\nNdMg7Cu2,TRUE\nNdMg7Ni2,TRUE\nNdMg8Cu,TRUE\nNdMg8Ni,TRUE\nNdMg9,FALSE\nNdMgCu3,TRUE\nNdNi,FALSE\nNi,FALSE\nNi10P19Pd71,TRUE\nNi11P2Pd7,TRUE\nNi12P5Pt3,FALSE\nNi12P5Pt8,TRUE\nNi13(B5C)2,TRUE\nNi13B12,FALSE\nNi14B10C,FALSE\nNi14B7C4,TRUE\nNi14P5Pd6,TRUE\nNi14P5Pt6,TRUE\nNi15(Mo3C2)2,TRUE\nNi15B2C3,FALSE\nNi15BC4,FALSE\nNi15Mo7C3,FALSE\nNi15MoP4,TRUE\nNi16(Mo2C)3,TRUE\nNi16B5C4,TRUE\nNi16B7C2,TRUE\nNi16BC3,FALSE\nNi16BP3,TRUE\nNi16Mo5C4,TRUE\nNi16Mo7C2,FALSE\nNi16P5Pd4,TRUE\nNi16P5Pt4,TRUE\nNi17(B3C)2,TRUE\nNi17(MoC)4,FALSE\nNi17(P3Pd8)3,TRUE\nNi17B23C10,TRUE\nNi17B2C,FALSE\nNi17B5C3,TRUE\nNi17B7C,TRUE\nNi17C3,FALSE\nNi17Mo5C3,TRUE\nNi18B5C2,FALSE\nNi18B6C,FALSE\nNi18B7,TRUE\nNi18BC,FALSE\nNi18Mo4C3,FALSE\nNi18Mo5C2,FALSE\nNi18P5Pd2,TRUE\nNi18P5Pt2,FALSE\nNi19(B2C)2,TRUE\nNi19(MoC)3,FALSE\nNi19B,FALSE\nNi19B25C6,TRUE\nNi19B29C2,FALSE\nNi19B6,FALSE\nNi19C,FALSE\nNi20B4C,TRUE\nNi20P19Pd61,TRUE\nNi21B21C8,TRUE\nNi21B23C6,TRUE\nNi21B25C4,FALSE\nNi21B4,FALSE\nNi22(B3C)7,TRUE\nNi22.5P25Pt52.5,TRUE\nNi23(B7C2)3,TRUE\nNi23B23C4,FALSE\nNi23B25C2,FALSE\nNi23B27,FALSE\nNi24B19C7,TRUE\nNi24B21C5,TRUE\nNi25B19C6,TRUE\nNi25B21C4,TRUE\nNi25B23C2,FALSE\nNi26B17C7,TRUE\nNi26B19C5,TRUE\nNi27B17C6,TRUE\nNi27B20C3,FALSE\nNi27B23,FALSE\nNi27Mo14C9,FALSE\nNi28B17C5,TRUE\nNi28B19C3,TRUE\nNi28B21C,TRUE\nNi29(B5C2)3,TRUE\nNi29(Mo2C)7,FALSE\nNi29(Mo4C3)3,FALSE\nNi29B20C,TRUE\nNi29B21,TRUE\nNi29B55C16,TRUE\nNi29Mo16C5,FALSE\nNi2P5Pd18,TRUE\nNi2PPd2,TRUE\nNi2PPt2,TRUE\nNi30B11C9,TRUE\nNi30B13C7,TRUE\nNi30B17C3,TRUE\nNi31B13C6,TRUE\nNi31B14C5,TRUE\nNi31B19,TRUE\nNi31Mo10C9,FALSE\nNi31Mo12C7,TRUE\nNi31Mo69,TRUE\nNi32B11C7,TRUE\nNi33B11C6,TRUE\nNi33B14C3,TRUE\nNi33B17,TRUE\nNi33B55C12,TRUE\nNi33B7C10,FALSE\nNi33B9C8,TRUE\nNi33Mo10C7,TRUE\nNi33Mo12C5,FALSE\nNi33Mo8C9,FALSE\nNi34B11C5,TRUE\nNi34B13C3,TRUE\nNi35(B3C2)3,TRUE\nNi35(Mo2C3)3,FALSE\nNi35B11C4,FALSE\nNi35B13C2,FALSE\nNi35B14C,TRUE\nNi35B7C8,FALSE\nNi36.5P27Pd36.5,TRUE\nNi36B13C,FALSE\nNi37.5P25Pd37.5,TRUE\nNi37.5P25Pt37.5,TRUE\nNi37B10C3,FALSE\nNi37B13,FALSE\nNi37B55C8,TRUE\nNi37B59C4,TRUE\nNi37B6P7,TRUE\nNi37B8C5,TRUE\nNi37P26Pd37,TRUE\nNi38(B3C)3,FALSE\nNi38.5P23Pd38.5,TRUE\nNi38B11C,FALSE\nNi38B5P7,TRUE\nNi39B10C,TRUE\nNi39B11,FALSE\nNi39B8C3,TRUE\nNi3B2,TRUE\nNi3B5C2,TRUE\nNi3P5Pt12,TRUE\nNi3PPd,TRUE\nNi40B3P7,TRUE\nNi40B9P,TRUE\nNi40P9W,TRUE\nNi41(B2C)3,FALSE\nNi41.5P17Pd41.5,TRUE\nNi41B5C4,FALSE\nNi41B8C,TRUE\nNi41B9,TRUE\nNi41P18Pd41,TRUE\nNi41P9,TRUE\nNi42.5P15Pd42.5,TRUE\nNi42B7C,FALSE\nNi43P14Pd43,TRUE\nNi47Mo53,TRUE\nNi4B,FALSE\nNi4C,FALSE\nNi4P,TRUE\nNi4P5Pt16,TRUE\nNi5(PPd4)19,TRUE\nNi52.5P25Pt22.5,TRUE\nNi53.5B44C2.5,FALSE\nNi53B41C6,FALSE\nNi55B42.5C2.5,FALSE\nNi59Mo41,TRUE\nNi63P20Pd17,TRUE\nNi66.5B17Mo16.5,TRUE\nNi66.5B17W16.5,TRUE\nNi67B17C16,FALSE\nNi68.5B17Mo14.5,TRUE\nNi68.5B17W14.5,TRUE\nNi68Mo13P19,TRUE\nNi69Mo12P19,TRUE\nNi6P5Pd14,TRUE\nNi6P5Pt14,TRUE\nNi6P5Pt9,TRUE\nNi70.5B17Mo12.5,TRUE\nNi70.5B17W12.5,TRUE\nNi71B15P14,TRUE\nNi72Mo9P19,TRUE\nNi73(B5C4)3,FALSE\nNi73B22C5,FALSE\nNi73Mo7P20,TRUE\nNi75B13C12,FALSE\nNi75B17C8,FALSE\nNi75B17W8,TRUE\nNi75P18W7,TRUE\nNi77B13C10,FALSE\nNi77P18W5,TRUE\nNi78.5B11.5C10,FALSE\nNi7B3,TRUE\nNi7BC2,FALSE\nNi7Mo2C,TRUE\nNi81.5B1.8P16.7,TRUE\nNi81.5B11.1P7.4,TRUE\nNi81.5B12P6.5,TRUE\nNi81.5B14.8P3.7,TRUE\nNi81.5B15P3.5,TRUE\nNi81.5B16.7P1.8,TRUE\nNi81.5B17P1.5,TRUE\nNi81.5B18.5,TRUE\nNi81.5B2P16.5,TRUE\nNi81.5B5.5P13,TRUE\nNi81.5P18.5,TRUE\nNi81B14C5,TRUE\nNi81P19,TRUE\nNi8BC,FALSE\nNi8BP,TRUE\nNi8P5Pd12,TRUE\nNi8P5Pt12,FALSE\nNi9C,FALSE\nNi9P2Pd9,TRUE\nNi9P5Pt6,TRUE\nNiPd,TRUE\nNiPd4,TRUE\nP19Ir40Pd41,TRUE\nP19Pd81,TRUE\nPr0.3Zr10Fe89.7,TRUE\nPr36B5Au9,TRUE\nPr3Zr5Fe42,TRUE\nPr67.5B10Au22.5,TRUE\nPrZr5Fe44,FALSE\nSb19.3Pb27.5Au53.2,TRUE\nSb22.5Pb22.5Au55,TRUE\nSc3Fe,TRUE\nScFe9,TRUE\nSi(BMo2)3,FALSE\nSi(Ni3B)6,TRUE\nSi(Ni5B)4,FALSE\nSi(Ni7B)3,FALSE\nSi10B17Mo73,TRUE\nSi10Ge7Pd83,TRUE\nSi10Ni73B17,TRUE\nSi11Ni78B11,TRUE\nSi11Pd39,TRUE\nSi12.5B17.5Mo70,TRUE\nSi12.5B20Mo67.5,TRUE\nSi12.5Ni75B12.5,TRUE\nSi12Ni67B21,TRUE\nSi13(GePd28)3,TRUE\nSi14Ni67B19,FALSE\nSi14Ni69B17,TRUE\nSi15(Ni4B)17,TRUE\nSi15Ni67.5C17.5,TRUE\nSi15Ni72B13,TRUE\nSi15Pd81Au4,TRUE\nSi16(Pd25Au3)3,TRUE\nSi16.5Ag1.7Pd81.8,TRUE\nSi16.5Ag10Pd73.5,TRUE\nSi16.5Ag12.5Pd71,TRUE\nSi16.5Ag15Pd68.5,TRUE\nSi16.5Ag20.9Pd62.6,FALSE\nSi16.5Ag4.2Pd79.3,TRUE\nSi16.5Ag4.5Pd79,TRUE\nSi16.5Ag4Pd79.5,TRUE\nSi16.5Ag5.5Pd78,TRUE\nSi16.5Ag6.7Pd76.8,TRUE\nSi16.5Ag6Pd77.5,TRUE\nSi16.5Ag8.5Pd75,TRUE\nSi16.5Ni1.7Pd81.8,TRUE\nSi16.5Ni10Pd73.5,TRUE\nSi16.5Ni11.7Pd71.8,TRUE\nSi16.5Ni12.5Pd71,TRUE\nSi16.5Ni15Pd68.5,TRUE\nSi16.5Ni19.2Pd64.3,TRUE\nSi16.5Ni20.9Pd62.6,TRUE\nSi16.5Ni26.7Pd56.8,TRUE\nSi16.5Ni29.2Pd54.3,TRUE\nSi16.5Ni35Pd48.5,TRUE\nSi16.5Ni4.2Pd79.3,TRUE\nSi16.5Ni40Pd43.5,TRUE\nSi16.5Ni43.4Pd40.1,TRUE\nSi16.5Ni50.1Pd33.4,TRUE\nSi16.5Ni58.5Pd25,FALSE\nSi16.5Ni6.7Pd76.8,TRUE\nSi16.5Pd62.6Au20.9,FALSE\nSi16.5Pd68.5Au15,TRUE\nSi16.5Pd71Au12.5,TRUE\nSi16.5Pd73.5Au10,TRUE\nSi16.5Pd76.5Au7,TRUE\nSi16.5Pd76.8Au6.7,TRUE\nSi16.5Pd76.8Rh6.7,FALSE\nSi16.5Pd76Au7.5,TRUE\nSi16.5Pd77.5Au6,TRUE\nSi16.5Pd78.5Au5,TRUE\nSi16.5Pd79.3Au4.2,TRUE\nSi16.5Pd79.3Rh4.2,TRUE\nSi16.5Pd79.5Au4,TRUE\nSi16.5Pd80.5Au3,TRUE\nSi16.5Pd80Au3.5,TRUE\nSi16.5Pd81.5Au2,TRUE\nSi16.5Pd81.8Au1.7,TRUE\nSi16.5Pd81.8Rh1.7,TRUE\nSi16.5Pd83.5,TRUE\nSi16Ag5Pd79,TRUE\nSi16Ni76.5B7.5,FALSE\nSi16Pd80.5Au3.5,TRUE\nSi17.5Ni67.5C15,TRUE\nSi17.6Pd82.4,TRUE\nSi17B12Mo71,TRUE\nSi17Pd71Au12,TRUE\nSi17Pd79Au4,TRUE\nSi18Ag5Pd77,TRUE\nSi18Ni16.4Pd65.6,TRUE\nSi18Ni32.8Pd49.2,TRUE\nSi18Ni49.2Pd32.8,TRUE\nSi18Ni69B13,FALSE\nSi18Ni8.2Pd73.8,TRUE\nSi18Pd75Au7,TRUE\nSi18Pd77Au5,TRUE\nSi18Pd79Au3,TRUE\nSi18Pd81Au,TRUE\nSi2(BMo5)3,TRUE\nSi2(Ni11B5)3,FALSE\nSi2(Ni5B)3,TRUE\nSi2(Ni5C)3,FALSE\nSi2.5B20Mo77.5,FALSE\nSi2.5Ni72.5B25,FALSE\nSi2.5Ni75.5B22,FALSE\nSi2.5Ni77.5B20,FALSE\nSi20Ag4.5Pd75.5,TRUE\nSi20Ni67.5C12.5,TRUE\nSi20Pd73Au7,TRUE\nSi21Pd75Au4,TRUE\nSi21Pd79,TRUE\nSi22.5B7.5Mo70,TRUE\nSi22.5Ni65C12.5,TRUE\nSi22.5Ni67.5C10,FALSE\nSi2B5Mo13,TRUE\nSi2BMo17,FALSE\nSi2BMo7,TRUE\nSi2BW7,TRUE\nSi2Ni16B7,FALSE\nSi2Ni17B6,TRUE\nSi2Ni17C,FALSE\nSi2Ni18B5,TRUE\nSi2Ni20B3,FALSE\nSi2Ni7C,FALSE\nSi3(Ni10B)2,FALSE\nSi3(Ni8B3)2,FALSE\nSi3(Ni9B2)2,TRUE\nSi3B2Mo15,TRUE\nSi3B3Mo14,TRUE\nSi3B4Mo13,FALSE\nSi3B5Mo12,FALSE\nSi3BMo16,FALSE\nSi3GePd21,TRUE\nSi3Ni13B4,TRUE\nSi3Ni14C3,FALSE\nSi3Ni15B2,TRUE\nSi3Ni15B7,FALSE\nSi3Ni15C2,FALSE\nSi3Ni16C,FALSE\nSi3Ni17,FALSE\nSi3Ni17B5,TRUE\nSi3Ni19B3,TRUE\nSi3Ni33B14,TRUE\nSi3Ni36B11,TRUE\nSi3Ni38B9,TRUE\nSi3Ni40B7,FALSE\nSi3Ni69B28,TRUE\nSi3Ni70B27,TRUE\nSi3Ni80B17,TRUE\nSi3Pd17,TRUE\nSi4(Ni6B)3,TRUE\nSi4B11Mo35,TRUE\nSi4B3Mo13,FALSE\nSi4BMo15,FALSE\nSi4BPd20,TRUE\nSi4Ni15C,FALSE\nSi4Ni17B4,FALSE\nSi4Ni39B7,TRUE\nSi4Pd21,TRUE\nSi5(B2Mo13)3,TRUE\nSi5(Ni11B4)3,TRUE\nSi5(Ni13B2)3,TRUE\nSi5B11Mo34,TRUE\nSi5B2Mo13,FALSE\nSi5BMo14,FALSE\nSi5Ni13C2,FALSE\nSi5Ni14C,FALSE\nSi5Ni38B7,TRUE\nSi5Pd17Au3,TRUE\nSi5Pd19Au,TRUE\nSi7(Ni24B7)3,TRUE\nSi7.5B20Mo72.5,TRUE\nSi7.5Ni70B22.5,TRUE\nSi7.5Ni75B17.5,TRUE\nSi7GePd42,TRUE\nSi7Ni36B7,TRUE\nSi7Ni38B5,TRUE\nSi7Ni76B17,TRUE\nSi8(Ni5B)7,TRUE\nSi8(Pd13Au)3,TRUE\nSi8.5Ni66B25.5,TRUE\nSi8B17Mo75,TRUE\nSi8Ni75B17,TRUE\nSi9(Ge2Au11)7,TRUE\nSi9.45Ge13.66Au76.89,TRUE\nSi9Ni36B5,FALSE\nSi9Ni38B3,FALSE\nSi9Pd36Au5,TRUE\nSi9Pd37Au4,TRUE\nSi9Pd38Au3,TRUE\nSi9Pd39Au2,TRUE\nSi9Pd40Au,TRUE\nSi9Pd41,TRUE\nSi9Pd8Au33,TRUE\nSiB2Mo17,FALSE\nSiB2Mo7,TRUE\nSiB3Mo16,FALSE\nSiB4Mo15,TRUE\nSiB5Mo14,FALSE\nSiBMo18,FALSE\nSiBMo3,FALSE\nSiBMo8,FALSE\nSiNi15B4,TRUE\nSiNi15C4,FALSE\nSiNi16C3,FALSE\nSiNi17B7,TRUE\nSiNi17C2,FALSE\nSiNi18C,FALSE\nSiNi19,FALSE\nSiNi19B5,TRUE\nSiNi36B13,TRUE\nSiNi4,FALSE\nSiNi7C2,FALSE\nSiNi8B,TRUE\nSiNi8C,FALSE\nSiNi9,FALSE\nSiNiPd3,TRUE\nSiPd4,TRUE\nSm1.3Fe79B19.7,TRUE\nSm10Al89Ni,TRUE\nSm11Al5Ni4,TRUE\nSm2(Al5Ni)3,TRUE\nSm2Al17Ni,TRUE\nSm2Al23,TRUE\nSm2Al7Ni,TRUE\nSm3Al14Ni3,TRUE\nSm3Al15Ni2,TRUE\nSm3Al16Ni,TRUE\nSm3Al22,TRUE\nSm3Al47,FALSE\nSm4Al13Ni3,TRUE\nSm4Al15Ni,FALSE\nSm4Al21,TRUE\nSm5Al87Ni8,TRUE\nSm5Fe77B18,TRUE\nSm6Al39Ni5,TRUE\nSm7(Al29Ni2)3,TRUE\nSm7Al43,TRUE\nSm7Al83Ni10,TRUE\nSm7Al85Ni8,TRUE\nSm9Al41,FALSE\nSm9Al81Ni10,TRUE\nSm9Al83Ni8,TRUE\nSm9Al85Ni6,TRUE\nSmAl15Ni4,FALSE\nSmAl16Ni3,TRUE\nSmAl17Ni2,TRUE\nSmAl18Ni,TRUE\nSmAl7Ni2,TRUE\nSmAl8Ni,TRUE\nSmAl9,TRUE\nSr1.5La61.5Cu37,TRUE\nSr10La53Cu37,TRUE\nSr10La61.5Cu28.5,TRUE\nSr11La52Cu37,TRUE\nSr11La60Cu29,TRUE\nSr12.5La50.5Cu37,TRUE\nSr12.5La57.5Cu30,TRUE\nSr13.5La56Cu30.5,TRUE\nSr14.5La53.5Cu32,TRUE\nSr14La49Cu37,TRUE\nSr14La55Cu31,TRUE\nSr15.5La51.5Cu33,TRUE\nSr15La48Cu37,TRUE\nSr15La52.5Cu32.5,TRUE\nSr16La47Cu37,TRUE\nSr17La47Cu36,TRUE\nSr17La48Cu35,TRUE\nSr2.5La60.5Cu37,TRUE\nSr2La71Cu27,TRUE\nSr3.5La59.5Cu37,TRUE\nSr3La70Cu27,TRUE\nSr4(La23Cu9)3,TRUE\nSr4La59Cu37,TRUE\nSr5La58Cu37,TRUE\nSr5La67.5Cu27.5,TRUE\nSr6.5La66Cu27.5,TRUE\nSr6La29Cu15,TRUE\nSr6La57Cu37,TRUE\nSr7.5La64.5Cu28,TRUE\nSr7La56Cu37,TRUE\nSr8.5La63.5Cu28,TRUE\nSr8La25Cu17,TRUE\nSr8La55Cu37,TRUE\nSr9La54Cu37,TRUE\nSr9La62.5Cu28.5,TRUE\nSrLa62Cu37,TRUE\nTa(NbNi2)3,TRUE\nTa10Ni31P9,TRUE\nTa10Ni73B17,TRUE\nTa12Ni71B17,TRUE\nTa13Ni70B17,TRUE\nTa2(Ti5Si)3,TRUE\nTa2Ni17P,TRUE\nTa2Ni3,TRUE\nTa3Nb13Si4,FALSE\nTa3Nb5Ni12,TRUE\nTa3NbNi6,TRUE\nTa3Ni7,TRUE\nTa40Ni59Ir,TRUE\nTa40Ni59Pd,TRUE\nTa40Ni59Ru,TRUE\nTa4Ni15P,TRUE\nTa4Ti13Si3,TRUE\nTa5(NbNi4)3,TRUE\nTa5(Ni4P)9,TRUE\nTa5CoNi4,TRUE\nTa6Ni13P,TRUE\nTa6Ti11Si3,TRUE\nTa7Fe83B10,TRUE\nTa7Ni13,TRUE\nTa8(Ti3Si)3,TRUE\nTaNb15Si4,TRUE\nTaNb7Ni12,TRUE\nTaNb7Si2,TRUE\nTaNbNi3,TRUE\nTaNi,TRUE\nTaNi4,TRUE\nTaNi9,TRUE\nTb1.3Fe79B19.7,TRUE\nTb15Fe76.5Co8.5,TRUE\nTb28.3Al15Fe56.7,FALSE\nTb28.3Fe56.7Si15,TRUE\nTb30(Fe9Co)7,TRUE\nTb30.8Al7.5Fe61.7,TRUE\nTb30.8Fe61.7Si7.5,TRUE\nTb32.5Al2.5Fe65,TRUE\nTb32.5Fe65Si2.5,TRUE\nTb33.3Fe66.7,FALSE\nTb3Al,TRUE\nTb5Fe77B18,TRUE\nTb67.5Al22.5B10,TRUE\nTi,FALSE\nTi(Al2Ni)3,TRUE\nTi(AlCu)2,FALSE\nTi(Co3B)6,TRUE\nTi(CuNi)2,FALSE\nTi(CuNi2)3,FALSE\nTi0.8Fe83.2B16,TRUE\nTi1.1Al98.9,FALSE\nTi10Al3Cu7,TRUE\nTi10Al9Cu,FALSE\nTi10Be7Si3,FALSE\nTi10Be9Si,FALSE\nTi10Co76.5B13.5,TRUE\nTi10Cu3Ni7,FALSE\nTi10CuNi9,FALSE\nTi10FeCu9,TRUE\nTi10Nb7Si3,TRUE\nTi10Si3Ni7,TRUE\nTi10SiNi9,FALSE\nTi10V7Si3,FALSE\nTi11(AlCu2)3,TRUE\nTi11(Be2Si)3,FALSE\nTi11(Nb2Si)3,TRUE\nTi11(SiNi2)3,TRUE\nTi11(V2Si)3,TRUE\nTi11Al2Cu7,TRUE\nTi11Al72Ni17,TRUE\nTi11Al9,FALSE\nTi11Be7Si2,FALSE\nTi11Be8Si,FALSE\nTi11Be9,FALSE\nTi11Cu9,TRUE\nTi11Ni9,TRUE\nTi11Si2Ni7,TRUE\nTi11Si4Ni5,FALSE\nTi11SiNi8,TRUE\nTi12Al3Cu5,TRUE\nTi12Al3Ni5,TRUE\nTi12Al5Cu8,TRUE\nTi12Al5Ni8,TRUE\nTi12Al7Cu,FALSE\nTi12Be5Si3,FALSE\nTi12Be7Si,TRUE\nTi12FeCu7,TRUE\nTi12Nb5Si3,TRUE\nTi12Si3Ni5,TRUE\nTi12Si5Ni8,TRUE\nTi12SiNi7,TRUE\nTi12V5Si3,TRUE\nTi13(Al15Ni14)3,TRUE\nTi13Al2Cu5,TRUE\nTi13Al2Ni5,TRUE\nTi13Al7,FALSE\nTi13Al70Ni17,TRUE\nTi13Al87,FALSE\nTi13Be4Si3,FALSE\nTi13Be5Si2,FALSE\nTi13Be6Si,TRUE\nTi13Be7,FALSE\nTi13Cu7,TRUE\nTi13Nb4Si3,TRUE\nTi13Ni67P20,TRUE\nTi13Ni7,TRUE\nTi13Si2Ni5,TRUE\nTi13Si3Ni4,TRUE\nTi13Si4Ni3,FALSE\nTi13SiNi6,TRUE\nTi13V4Si3,TRUE\nTi14(BeSi)3,FALSE\nTi14(NbSi)3,TRUE\nTi14(SiNi)3,TRUE\nTi14(VSi)3,TRUE\nTi14Al5Cu,FALSE\nTi14Be5Si,TRUE\nTi14Si4Ni7,TRUE\nTi14SiNi5,TRUE\nTi15(Nb4Si)17,TRUE\nTi15(Nb4Si)7,TRUE\nTi15Al13Ni22,TRUE\nTi15Al19Ni16,TRUE\nTi15Be2Si3,FALSE\nTi15Be3Si2,FALSE\nTi15Be4Si,FALSE\nTi15Co72.25B12.75,TRUE\nTi15Cu3Ni2,FALSE\nTi15CuNi4,TRUE\nTi15Nb26Si9,TRUE\nTi15Nb27Si8,TRUE\nTi15Nb2Si3,TRUE\nTi15Si2Ni3,TRUE\nTi15Si3Ni2,TRUE\nTi15Si4Ni,FALSE\nTi15SiNi4,TRUE\nTi15V2Si3,TRUE\nTi15VSi4,TRUE\nTi16Al19Ni15,TRUE\nTi16Al47Ni37,TRUE\nTi16Al9,FALSE\nTi16Cu3Ni,FALSE\nTi16CuNi3,FALSE\nTi16NbSi3,TRUE\nTi16P19Pd65,TRUE\nTi16Si3Ni,TRUE\nTi16Si5Ni4,TRUE\nTi16SiNi3,FALSE\nTi16SiNi8,TRUE\nTi16VSi3,TRUE\nTi17(Al9Ni2)3,TRUE\nTi17Al33,TRUE\nTi17Al35Ni48,TRUE\nTi17Cu33,FALSE\nTi17CuNi2,FALSE\nTi17Ni3,FALSE\nTi17Si2Ni,FALSE\nTi17Si3,TRUE\nTi17SiNi2,FALSE\nTi17VSi2,FALSE\nTi18CuNi,FALSE\nTi18Fe3Si4,TRUE\nTi18Ni7,TRUE\nTi19Al29Ni52,TRUE\nTi19Al31,TRUE\nTi19Al31Ni50,FALSE\nTi19Si,FALSE\nTi2(Co13B3)3,TRUE\nTi2(Nb5Si)3,TRUE\nTi2.1Ni78.8B19.1,TRUE\nTi2.9Al97.1,FALSE\nTi20(Al3Ni7)3,TRUE\nTi20P19Pd61,TRUE\nTi21Al15Ni14,TRUE\nTi21Al22Ni7,TRUE\nTi21Nb22Cu57,TRUE\nTi22(Al3Ni)7,TRUE\nTi22Al43Ni35,TRUE\nTi22Al53Ni25,TRUE\nTi23(Al9Ni2)7,TRUE\nTi23Al40Ni37,TRUE\nTi23Al67Ni10,TRUE\nTi23Nb20Cu57,TRUE\nTi26(Nb5Si3)3,TRUE\nTi26Al57Ni17,TRUE\nTi27Al23,TRUE\nTi27Al5Ni18,TRUE\nTi27Cu73,TRUE\nTi27Nb15Si8,TRUE\nTi28(Nb5Cu19)3,TRUE\nTi28.8Nb33Cu38.2,TRUE\nTi28Nb15Si7,TRUE\nTi28Nb47Si25,FALSE\nTi29(Nb5Si2)3,FALSE\nTi29Be21,FALSE\nTi2Al11Cu7,FALSE\nTi2Al23,FALSE\nTi2Al2Cu,FALSE\nTi2Al3,FALSE\nTi2Al3Cu5,TRUE\nTi2Al5Cu3,FALSE\nTi2Al7Cu,FALSE\nTi2AlCu,FALSE\nTi2AlCu7,FALSE\nTi2AlNi,TRUE\nTi2AlNi2,TRUE\nTi2AlNi7,FALSE\nTi2Co17B6,TRUE\nTi2Co18B5,TRUE\nTi2Co37B11,TRUE\nTi2Cu2Ni,TRUE\nTi2Cu3,TRUE\nTi2Cu3Ni5,FALSE\nTi2Cu5Ni3,FALSE\nTi2Cu7Ni,FALSE\nTi2CuNi,TRUE\nTi2CuNi2,FALSE\nTi2CuNi7,FALSE\nTi2Ni3,TRUE\nTi2P19Pd79,TRUE\nTi2Si3Ni5,FALSE\nTi2SiNi2,TRUE\nTi3(Co8B3)2,TRUE\nTi3.36Fe80.64B16,TRUE\nTi3.5Al95.8Ni0.7,FALSE\nTi3.8Ni78B18.2,TRUE\nTi30.1Nb30Cu39.9,TRUE\nTi31Be19,TRUE\nTi31Ni15B4,TRUE\nTi31Ni19,TRUE\nTi32.3Nb25Cu42.7,TRUE\nTi32Al59Ni9,TRUE\nTi33Nb10Cu57,TRUE\nTi34.4Nb20Cu45.6,TRUE\nTi36.6Nb15Cu48.4,TRUE\nTi37Al52Ni11,TRUE\nTi37Nb50Si13,FALSE\nTi37Ni63,TRUE\nTi38.7Nb10Cu51.3,TRUE\nTi38Nb5Cu57,TRUE\nTi39Si11,TRUE\nTi3Al,FALSE\nTi3Al2,FALSE\nTi3Al2Cu5,TRUE\nTi3Al3Cu4,FALSE\nTi3Al4Cu3,FALSE\nTi3Al5Cu2,FALSE\nTi3Al6Cu,FALSE\nTi3Al7,FALSE\nTi3Al7Cu10,TRUE\nTi3Al9Cu8,FALSE\nTi3AlCu,FALSE\nTi3AlCu6,TRUE\nTi3AlNi,TRUE\nTi3Be2,TRUE\nTi3Co17B5,TRUE\nTi3Cu17,FALSE\nTi3Cu2,TRUE\nTi3Cu2Ni5,FALSE\nTi3Cu3Ni4,FALSE\nTi3Cu4Ni3,TRUE\nTi3Cu5Ni2,TRUE\nTi3Cu6Ni,TRUE\nTi3Cu7,TRUE\nTi3CuNi,TRUE\nTi3CuNi6,FALSE\nTi3Nb14Si3,TRUE\nTi3Ni,FALSE\nTi3Ni13P4,TRUE\nTi3Ni2,TRUE\nTi3Ni7,FALSE\nTi3Ni77P20,TRUE\nTi3NiP,TRUE\nTi3Si,FALSE\nTi3Si17,TRUE\nTi3Si2Ni5,FALSE\nTi3Si3Ni4,FALSE\nTi3Si4Ni3,FALSE\nTi3SiNi,FALSE\nTi3VSi,FALSE\nTi4(AlCu)3,FALSE\nTi4(CuNi)3,TRUE\nTi4(SiNi)3,FALSE\nTi40.9Nb5Cu54.1,TRUE\nTi40Al43Ni17,TRUE\nTi40Nb47Si13,FALSE\nTi41Al59,TRUE\nTi42(AlNi)29,TRUE\nTi42.6Nb1Cu56.4,TRUE\nTi42Al23Ni35,TRUE\nTi42Al51Ni7,TRUE\nTi42NbCu57,TRUE\nTi43Al57,TRUE\nTi45Al36Ni19,TRUE\nTi48Al45Ni7,TRUE\nTi4Al,FALSE\nTi4Al10Ni11,TRUE\nTi4Al21,FALSE\nTi4Al5Cu,FALSE\nTi4Al5Cu11,TRUE\nTi4Al7Cu9,FALSE\nTi4Al9Cu7,FALSE\nTi4AlCu5,TRUE\nTi4Be,FALSE\nTi4Co16B5,TRUE\nTi4Co35B11,TRUE\nTi4Co37B9,TRUE\nTi4Cu,FALSE\nTi4Cu5Ni,TRUE\nTi4CuNi5,FALSE\nTi4Nb13Si3,TRUE\nTi4Ni,FALSE\nTi4Ni21,FALSE\nTi4Si,TRUE\nTi4Si5Ni16,TRUE\nTi4SiNi5,TRUE\nTi5(AlCu4)3,TRUE\nTi5(Nb4Si)3,TRUE\nTi5.9Al94.1,FALSE\nTi50Cu13Ni37,FALSE\nTi51Al15Cu34,TRUE\nTi52.5Nb30Si17.5,TRUE\nTi57.5Nb25Si17.5,TRUE\nTi57Al5Cu38,TRUE\nTi57Be43,FALSE\nTi57Nb30Si13,FALSE\nTi58(Al5Ni)7,TRUE\nTi59Be41,TRUE\nTi5Al2Cu3,TRUE\nTi5Al2Ni3,TRUE\nTi5Al3Cu2,FALSE\nTi5Al41Ni54,FALSE\nTi5Al4Cu,FALSE\nTi5Al54Ni41,FALSE\nTi5Al7Cu8,FALSE\nTi5AlNi4,TRUE\nTi5Be4Si,FALSE\nTi5Co17B3,TRUE\nTi5Cu2Ni3,TRUE\nTi5Cu3Ni2,TRUE\nTi5Cu4Ni,TRUE\nTi5CuNi4,FALSE\nTi5FeCu4,TRUE\nTi5Nb3Si2,FALSE\nTi5Si2Ni3,TRUE\nTi5SiNi4,TRUE\nTi6(Co3B)11,TRUE\nTi6(CuNi)7,FALSE\nTi61Be39,TRUE\nTi61Cu16Ni23,TRUE\nTi62.5Be37.5,TRUE\nTi63Be37,TRUE\nTi67.5Nb15Si17.5,TRUE\nTi67Ni33,TRUE\nTi6Al3Cu,FALSE\nTi6Al9Ni5,TRUE\nTi6AlCu3,TRUE\nTi6AlNi3,TRUE\nTi6Be3Si,FALSE\nTi6Co35B9,TRUE\nTi6Cu3Ni,TRUE\nTi6CuNi3,TRUE\nTi6Nb11Si3,TRUE\nTi6Nb3Si,FALSE\nTi6SiNi3,TRUE\nTi7Al11Cu2,FALSE\nTi7Al12Cu,FALSE\nTi7Al13,FALSE\nTi7Al2Cu,FALSE\nTi7Al3,FALSE\nTi7Al3Cu10,TRUE\nTi7Al9Cu4,FALSE\nTi7AlCu12,TRUE\nTi7AlCu2,FALSE\nTi7Be2Si,TRUE\nTi7Be3,FALSE\nTi7Co2B,TRUE\nTi7Cu2Ni,TRUE\nTi7Cu3,FALSE\nTi7CuNi2,TRUE\nTi7Fe2B,TRUE\nTi7Fe82B11,TRUE\nTi7Fe83B10,TRUE\nTi7Nb10Si3,TRUE\nTi7Nb2Si,FALSE\nTi7Ni13,FALSE\nTi7Ni18,FALSE\nTi7Ni2B,TRUE\nTi7Ni3,TRUE\nTi7Si2Ni,FALSE\nTi7SiNi2,TRUE\nTi7V2Si,FALSE\nTi7VSi2,TRUE\nTi8(Co11B3)3,TRUE\nTi8(Nb3Si)3,TRUE\nTi8(SiNi3)3,TRUE\nTi87Si13,TRUE\nTi8Al17,TRUE\nTi8Al5Cu7,TRUE\nTi8Al5Ni7,TRUE\nTi8AlCu,FALSE\nTi8AlCu11,TRUE\nTi8Co31B11,TRUE\nTi8CuNi,FALSE\nTi8FeCu11,TRUE\nTi8NbSi,FALSE\nTi8Ni17,TRUE\nTi8P19Pd73,TRUE\nTi8Si5Ni12,TRUE\nTi8SiNi,TRUE\nTi8SiNi11,TRUE\nTi9Al,FALSE\nTi9Al10Cu,FALSE\nTi9Al11,FALSE\nTi9Al2Ni9,FALSE\nTi9Al3Cu8,TRUE\nTi9Al4Cu7,TRUE\nTi9Al5Cu6,FALSE\nTi9Al5Ni6,TRUE\nTi9Al6Ni5,TRUE\nTi9Al9Cu2,FALSE\nTi9Al9Ni7,TRUE\nTi9AlCu10,TRUE\nTi9AlNi10,FALSE\nTi9Be,FALSE\nTi9Cu,FALSE\nTi9Cu11,TRUE\nTi9Cu9Ni2,TRUE\nTi9Nb8Si3,TRUE\nTi9Ni,FALSE\nTi9Ni11,FALSE\nTi9Si,FALSE\nTi9Si2Ni9,FALSE\nTi9Si3Ni8,TRUE\nTi9Si4Ni7,TRUE\nTi9SiNi10,FALSE\nTi9V8Si3,TRUE\nTiAl10Cu9,TRUE\nTiAl11Cu8,TRUE\nTiAl12Cu7,FALSE\nTiAl2Cu7,FALSE\nTiAl2Ni,TRUE\nTiAl3Cu,FALSE\nTiAl4,FALSE\nTiAl4Cu5,TRUE\nTiAl4Ni5,FALSE\nTiAl5Cu4,TRUE\nTiAl9,FALSE\nTiAlCu2,TRUE\nTiAlCu3,TRUE\nTiBe,FALSE\nTiCo19B5,TRUE\nTiCu,TRUE\nTiCu2Ni7,FALSE\nTiCu3,TRUE\nTiCu4,FALSE\nTiCu5Ni4,FALSE\nTiCu7Ni2,FALSE\nTiCu8Ni,FALSE\nTiCu9,FALSE\nTiCuNi3,FALSE\nTiCuNi8,FALSE\nTiFe15B4,TRUE\nTiFe19B5,TRUE\nTiNb16Si3,TRUE\nTiNb2Si,FALSE\nTiNi,FALSE\nTiNi15P4,TRUE\nTiNi19P5,TRUE\nTiNi3,FALSE\nTiNi7P2,TRUE\nTiNi9,FALSE\nTiSi4,TRUE\nU20.6Si20.6Pd58.8,TRUE\nV10Co76.5B13.5,TRUE\nV15Co72.25B12.75,TRUE\nV15Fe69B16,TRUE\nV15Fe71B14,TRUE\nV15Fe73B12,FALSE\nV25Co63.75B11.25,TRUE\nV3Fe15B2,FALSE\nV4(Fe25B7)3,TRUE\nV5(Fe13B2)3,TRUE\nV5(Fe14B)3,FALSE\nV5Co17B3,TRUE\nV5Co80.75B14.25,TRUE\nV5Fe37B8,TRUE\nV5Fe38B7,TRUE\nV5Fe41B4,FALSE\nV5Fe43B2,FALSE\nV5Fe79B16,TRUE\nV5Fe81B14,TRUE\nV5Fe83B12,TRUE\nV5Fe87B8,FALSE\nV5Fe89B6,FALSE\nV5Fe91B4,FALSE\nV7Fe76P17,TRUE\nV7Fe79B14,TRUE\nV9Fe74P17,TRUE\nVFe15B4,TRUE\nVFe17B2,FALSE\nVFe39B10,TRUE\nVFe8B,FALSE\nY(CoB)2,TRUE\nY(Mg23Cu10)3,TRUE\nY(Mg28Cu5)3,FALSE\nY(Mg2Ag)3,TRUE\nY(Mg2Cu)3,TRUE\nY(Mg2Ni)3,TRUE\nY(MgAg)2,TRUE\nY(MgCu)2,TRUE\nY(MgNi)2,FALSE\nY10(Al29Ni)3,TRUE\nY10Mg89Cu,FALSE\nY11Al5Ni4,TRUE\nY11Al89,TRUE\nY12.5Mg77.5Mn10,FALSE\nY12.5Mg87.5,FALSE\nY12Al5Cu8,TRUE\nY12Mg5Cu8,TRUE\nY13Al82Ni5,TRUE\nY13Al87,TRUE\nY15Mg48Cu37,TRUE\nY15Mg81Mn4,FALSE\nY15Mg83Mn2,FALSE\nY15Mg84Cu,TRUE\nY2(Al5Ni)3,TRUE\nY2(Mg5Cu)3,TRUE\nY2(Mg5Ni)3,TRUE\nY2.5Mg87.5Mn10,FALSE\nY2.5Mg89.5Mn8,FALSE\nY2.5Mg91.5Mn6,TRUE\nY2.5Mg93.5Mn4,FALSE\nY2.5Mg95.5Mn2,FALSE\nY20Mg79Cu,FALSE\nY21Al15Cu14,TRUE\nY27Al5Cu18,TRUE\nY2Al17Ni,TRUE\nY2Al23,TRUE\nY2Al5Ni3,TRUE\nY2Al7Ni,FALSE\nY2Mg13Ag5,TRUE\nY2Mg13Cu5,TRUE\nY2Mg13Ni5,TRUE\nY2Mg17Ag,FALSE\nY2Mg17Cu,TRUE\nY2Mg17Ni,TRUE\nY2Mg2Ag,TRUE\nY2Mg3Ag5,TRUE\nY2Mg5Ag3,TRUE\nY2Mg5Cu3,TRUE\nY2Mg5Ni3,TRUE\nY2Mg7Ag,TRUE\nY2Mg7Cu,TRUE\nY2Mg7Ni,FALSE\nY2MgAg2,FALSE\nY2MgCu2,FALSE\nY2MgNi2,TRUE\nY3(Al10Cu)2,TRUE\nY3(Mg10Cu)2,TRUE\nY3Al12Ni5,TRUE\nY3Al13Ni4,TRUE\nY3Al14Ni3,TRUE\nY3Al15Ni2,TRUE\nY3Al16Ni,FALSE\nY3Al17,TRUE\nY3Al22,TRUE\nY3Al87Ni10,TRUE\nY3Al88Ni9,TRUE\nY3Cu2,TRUE\nY3Mg11Ag6,TRUE\nY3Mg12Ag5,TRUE\nY3Mg12Cu5,TRUE\nY3Mg12Ni5,TRUE\nY3Mg13Ni4,TRUE\nY3Mg14Cu3,TRUE\nY3Mg14Ni3,TRUE\nY3Mg15Cu2,TRUE\nY3Mg15Ni2,TRUE\nY3Mg16Ag,TRUE\nY3Mg16Ni,FALSE\nY3Mg17,TRUE\nY3Mg2Ag5,FALSE\nY3Mg3Ag4,TRUE\nY3Mg3Cu4,TRUE\nY3Mg3Ni4,TRUE\nY3Mg4Ag3,TRUE\nY3Mg4Cu3,TRUE\nY3Mg4Ni3,TRUE\nY3Mg5Ag2,TRUE\nY3Mg5Cu2,TRUE\nY3Mg5Ni2,TRUE\nY3Mg6Ag,TRUE\nY3Mg6Cu,FALSE\nY3MgAg,FALSE\nY4(MgAg)3,TRUE\nY4(MgCu)3,FALSE\nY4Al11Ni5,TRUE\nY4Al13Ni3,FALSE\nY4Al15Ni,FALSE\nY4Mg13Ni3,TRUE\nY4Mg15Cu,FALSE\nY4Mg21,TRUE\nY4Mg5Ag,FALSE\nY5(Mg14Mn)3,TRUE\nY51Al15Cu34,TRUE\nY57Al5Cu38,TRUE\nY5Al41Ni4,TRUE\nY5Mg13Cu2,TRUE\nY5Mg2Ag3,FALSE\nY5Mg3Ag2,TRUE\nY5Mg41Mn4,FALSE\nY5Mg43Mn2,TRUE\nY5Mg44Mn,TRUE\nY5Mg87Mn8,TRUE\nY5Mg89Mn6,TRUE\nY5Mg91Mn4,TRUE\nY5Mg93Mn2,FALSE\nY6Mg13Cu,FALSE\nY6Mg15Cu4,TRUE\nY6Mg43Mn,TRUE\nY7(Al26Ni5)3,TRUE\nY7.5Mg82.5Mn10,FALSE\nY7.5Mg84.5Mn8,FALSE\nY7.5Mg86.5Mn6,TRUE\nY7.5Mg88.5Mn4,TRUE\nY7.5Mg90.5Mn2,FALSE\nY7Al43,TRUE\nY8Al87Ni5,TRUE\nY9(Mg5Cu3)2,TRUE\nY9Al85Cu6,TRUE\nY9Al91,TRUE\nYAl15Ni4,FALSE\nYAl16Ni3,TRUE\nYAl17Ni2,TRUE\nYAl18Ni,TRUE\nYAl3Ni,TRUE\nYAl44Ni5,TRUE\nYAl7Ni2,TRUE\nYAl8Ni,TRUE\nYAl9,TRUE\nYMg11Cu8,TRUE\nYMg13Ni6,TRUE\nYMg14Ag5,TRUE\nYMg14Cu5,TRUE\nYMg15Ni4,TRUE\nYMg16Ag3,TRUE\nYMg16Cu3,TRUE\nYMg16Mn3,FALSE\nYMg16Ni3,TRUE\nYMg17Ag2,FALSE\nYMg17Cu2,TRUE\nYMg17Ni2,TRUE\nYMg18Ag,FALSE\nYMg18Cu,FALSE\nYMg18Ni,FALSE\nYMg19,FALSE\nYMg3,FALSE\nYMg3Ag,TRUE\nYMg3Cu,TRUE\nYMg3Ni,TRUE\nYMg4,FALSE\nYMg4Ag5,FALSE\nYMg59Cu40,TRUE\nYMg5Ag4,TRUE\nYMg5Ni4,FALSE\nYMg79Cu20,TRUE\nYMg7Ag2,TRUE\nYMg7Cu2,TRUE\nYMg7Ni2,TRUE\nYMg89Cu10,FALSE\nYMg8Ag,TRUE\nYMg8Cu,TRUE\nYMg8Ni,TRUE\nYMg9,FALSE\nYMgAg3,FALSE\nYb11Cu39,TRUE\nYb18Cu7,TRUE\nYb20.22Ce25.73Cu54.05,TRUE\nYb28.42Ce20.56Cu51.02,TRUE\nYb9Cu41,TRUE\nZn29Cu70Pb,TRUE\nZr(Al2Ni)3,TRUE\nZr(AlNi)2,FALSE\nZr(AlNi2)3,FALSE\nZr(CrCo2)3,TRUE\nZr(CuNi)2,FALSE\nZr(Fe2Co)3,TRUE\nZr(Fe5B)4,TRUE\nZr(FeCo2)3,TRUE\nZr10(Fe7Co3)9,TRUE\nZr10(Fe7Ni3)9,TRUE\nZr10(Fe9Co)9,TRUE\nZr10(Fe9Ni)9,TRUE\nZr10(FeNi9)9,TRUE\nZr10.2V10.6Co79.2,TRUE\nZr10.4Cr10.6Co79,TRUE\nZr10.5Co79.5Mo10,TRUE\nZr10.5Co80Mo9.5,TRUE\nZr10.8Cr11.2Co78,TRUE\nZr10Al0.018Fe89.982,TRUE\nZr10Al0.036Fe89.964,TRUE\nZr10Al0.054Fe89.946,TRUE\nZr10Al0.09Fe89.91,TRUE\nZr10Al22.5Fe67.5,TRUE\nZr10Al3Ni7,TRUE\nZr10AlNi9,TRUE\nZr10Cr17.1Co72.9,TRUE\nZr10Cr17Fe73,TRUE\nZr10Cr3Ni7,TRUE\nZr10Cr7Fe83,TRUE\nZr10Cu7Ni3,TRUE\nZr10Cu9B,TRUE\nZr10Fe22.5Co67.5,TRUE\nZr10Fe67.5Co22.5,TRUE\nZr10Fe76.5Ni13.5,TRUE\nZr10Fe89.91Ge0.09,TRUE\nZr10Fe89.91Si0.09,TRUE\nZr10Fe89.946Ge0.054,TRUE\nZr10Fe89.946Si0.054,TRUE\nZr10Fe89.964Ge0.036,TRUE\nZr10Fe89.964Si0.036,TRUE\nZr10Fe89.982Ge0.018,TRUE\nZr10Fe89.982Si0.018,TRUE\nZr10Ni73B17,TRUE\nZr10Ti3Si7,TRUE\nZr10Ti4Cu11,TRUE\nZr10Ti7Si3,TRUE\nZr10V0.018Fe89.982,TRUE\nZr10V0.036Fe89.964,TRUE\nZr10V0.054Fe89.946,TRUE\nZr10V0.09Fe89.91,TRUE\nZr11(Al2Ni)3,TRUE\nZr11(AlNi2)3,TRUE\nZr11(Cu2Ni)3,TRUE\nZr11(CuNi2)3,TRUE\nZr11(Nb2Ge)3,TRUE\nZr11(Nb2Si)3,TRUE\nZr11(Ta2Si)3,TRUE\nZr11(Ti2Si)3,TRUE\nZr11(TiSi2)3,TRUE\nZr11(V2Si)3,TRUE\nZr11.2Co78Mo10.8,TRUE\nZr11.2Co82.2W6.6,TRUE\nZr11.4Cr11.6Co77,TRUE\nZr11.5Co74.5W14,TRUE\nZr11.5Fe84B4.5,TRUE\nZr11Al2Ni7,TRUE\nZr11Al4Cu5,TRUE\nZr11Al4Ni5,TRUE\nZr11Al57Ni32,TRUE\nZr11Al5Co4,TRUE\nZr11Al5Ni4,TRUE\nZr11AlNi8,TRUE\nZr11Be7Nb2,TRUE\nZr11Be9,TRUE\nZr11Cu14,TRUE\nZr11Cu5Ni4,TRUE\nZr11Cu7B2,TRUE\nZr11Cu8B,TRUE\nZr11Fe89,TRUE\nZr11Nb8Si,FALSE\nZr11Ti22Cu17,FALSE\nZr11Ti4Si5,TRUE\nZr11Ti5Si4,TRUE\nZr12.2V12Co75.8,TRUE\nZr12.5Co74.5Mo13,TRUE\nZr12.5Co80.5W7,TRUE\nZr12Al3Cu5,TRUE\nZr12Al3Ni5,TRUE\nZr12Al5Ni3,TRUE\nZr12Al7Ni,FALSE\nZr12Al8Ni5,TRUE\nZr12AlNi7,TRUE\nZr12Be5Nb3,FALSE\nZr12Be7Nb,TRUE\nZr12Cr12.6Co75.4,TRUE\nZr12Cr3Ni5,TRUE\nZr12Cu3Ni5,TRUE\nZr12Cu5Ni3,TRUE\nZr12Cu7B,TRUE\nZr12Fe75B13,TRUE\nZr12Fe83B5,TRUE\nZr12Fe85B3,TRUE\nZr12Ti23Si65,TRUE\nZr12Ti3Si5,TRUE\nZr12Ti5Si3,TRUE\nZr12V15Ni23,TRUE\nZr13(Al19Ni10)3,TRUE\nZr13(Al2Ni)4,TRUE\nZr13(Ti4Si25)3,TRUE\nZr13(TiSi5)2,TRUE\nZr13Al2Cu5,TRUE\nZr13Al2Ni5,TRUE\nZr13Al3Cu4,TRUE\nZr13Al3Ni4,TRUE\nZr13Al4Cu3,TRUE\nZr13Al4Ni3,TRUE\nZr13Al5Ni2,TRUE\nZr13AlCu6,TRUE\nZr13AlNi6,TRUE\nZr13Be4Nb3,FALSE\nZr13Be5Nb2,FALSE\nZr13Be6Nb,TRUE\nZr13Be7,TRUE\nZr13Co5Pd2,TRUE\nZr13Co6Pd,TRUE\nZr13Co74W13,TRUE\nZr13Cr4Si3,TRUE\nZr13Cu5B2,TRUE\nZr13Cu6B,TRUE\nZr13Fe85B2,TRUE\nZr13Fe87,FALSE\nZr13Ge3Mo4,TRUE\nZr13Nb4Ge3,TRUE\nZr13Nb4Si3,TRUE\nZr13Nb6Si,FALSE\nZr13Si3Mo4,TRUE\nZr13Ta4Ge3,TRUE\nZr13Ta4Si3,TRUE\nZr13Ti3Si4,TRUE\nZr13Ti4Ge3,TRUE\nZr13Ti4Si3,TRUE\nZr13V10Ni27,TRUE\nZr13V2Ni5,TRUE\nZr13V4Ge3,TRUE\nZr13V4Si3,TRUE\nZr14(Al5Ni7)3,TRUE\nZr14(AlFe)3,TRUE\nZr14(AlNi)3,TRUE\nZr14(AlNi3)9,TRUE\nZr14(CrNi)3,TRUE\nZr14(MnAl)3,TRUE\nZr14(SiMo)3,TRUE\nZr14(TiSi)3,TRUE\nZr14.5Co65.5Mo20,TRUE\nZr14.5V18Co67.5,TRUE\nZr14.8V16Co69.2,TRUE\nZr14Al11Ni25,TRUE\nZr14Al13Ni23,TRUE\nZr14Al5Ni,TRUE\nZr14AlNi5,TRUE\nZr14Cu5B,TRUE\nZr14Ni7B4,TRUE\nZr15(Ni3B2)2,TRUE\nZr15(Ni4B)2,TRUE\nZr15.2V12Co72.8,TRUE\nZr15.4Co68.6Mo16,TRUE\nZr15.5V10Co74.5,TRUE\nZr15.6Co76.4W8,TRUE\nZr15.7Co70.3Mo14,TRUE\nZr15.7V8Co76.3,TRUE\nZr15.8Co78.2W6,TRUE\nZr15Al17Ni18,TRUE\nZr15Al2Ni3,TRUE\nZr15Al3Ni2,TRUE\nZr15Al3Ni32,TRUE\nZr15Al57Ni28,TRUE\nZr15Al7Ni3,TRUE\nZr15AlNi4,TRUE\nZr15Co67Mo18,TRUE\nZr15Cr2Si3,TRUE\nZr15Cu4B,TRUE\nZr15Cu4Ni,FALSE\nZr15CuNi4,FALSE\nZr15Fe2Si3,TRUE\nZr15Fe72B13,TRUE\nZr15Fe82B3,FALSE\nZr15Ge3Mo2,TRUE\nZr15Nb2Ge3,TRUE\nZr15Nb2Si3,TRUE\nZr15Ni9B,TRUE\nZr15Si302,TRUE\nZr15Si3Mo2,TRUE\nZr15Si3Ru2,TRUE\nZr15Ta2Si3,TRUE\nZr15Ti2Si3,TRUE\nZr15Ti3Si2,TRUE\nZr15Ti4Si,TRUE\nZr15V14Co71,TRUE\nZr15V2Ge3,TRUE\nZr15V2Si3,TRUE\nZr16(AlNi)17,TRUE\nZr16(Co11B)7,TRUE\nZr16.3Co75.7Mo8,TRUE\nZr16.3Co79.7Mo4,TRUE\nZr16.5Co77.5Mo6,TRUE\nZr16.5Cr16Co67.5,TRUE\nZr16Al3Ni,TRUE\nZr16AlNi3,TRUE\nZr16AlNi33,TRUE\nZr16Co71B13,TRUE\nZr16Cu3B,TRUE\nZr16Ni9,TRUE\nZr16Si3Mo,TRUE\nZr16Ti3Si,TRUE\nZr16TiSi3,TRUE\nZr17(Al6Ni5)3,TRUE\nZr17(Ni3P)2,TRUE\nZr17(SiNi3)2,TRUE\nZr17.5Cr10Co72.5,TRUE\nZr17.5Cr4Co78.5,TRUE\nZr17.5Cr6Co76.5,TRUE\nZr17.5Cr8Co74.5,TRUE\nZr17.5Cu80B2.5,TRUE\nZr17Al2Ni,FALSE\nZr17Al57Ni26,TRUE\nZr17Al59Ni24,TRUE\nZr17Al65Ni18,TRUE\nZr17AlNi2,TRUE\nZr17Cr12Co71,TRUE\nZr17Cr14Co69,TRUE\nZr17Cr2Co81,TRUE\nZr17Ge3,TRUE\nZr17Si3,TRUE\nZr17Ti13Si20,TRUE\nZr17Ti3,TRUE\nZr17Ti8Cu75,FALSE\nZr18Cu7,FALSE\nZr18Ni6P,TRUE\nZr18Ni7,TRUE\nZr18SiNi6,TRUE\nZr18Ti35Cu47,TRUE\nZr19Cu31,TRUE\nZr19Fe6,TRUE\nZr19Ti11Si70,TRUE\nZr2(AlNi5)3,FALSE\nZr2(CrCo5)3,TRUE\nZr2(CrFe5)3,TRUE\nZr2(Fe5B)3,TRUE\nZr2(FeCo)9,TRUE\nZr2(Ti5Si)3,TRUE\nZr2(TiSi5)3,TRUE\nZr2.5Nb8.5Co89,TRUE\nZr21(AlNi)2,TRUE\nZr21Al17Ni12,TRUE\nZr21AlNi3,TRUE\nZr21Cu28P,TRUE\nZr21Nb22Cu57,TRUE\nZr21Ti24Si55,TRUE\nZr21Ti4Si25,TRUE\nZr22.5Cu75B2.5,FALSE\nZr22Ti13Si15,TRUE\nZr23Al17Ni10,TRUE\nZr23Nb20Cu57,TRUE\nZr23Ti5Cu22,TRUE\nZr23V30Ni47,TRUE\nZr24.5V25Ni50.5,TRUE\nZr24Cu75B,FALSE\nZr27.5Cu70B2.5,TRUE\nZr27Cu23,FALSE\nZr27V20Ni53,TRUE\nZr28(Nb5Cu19)3,TRUE\nZr28.8Nb33Cu38.2,TRUE\nZr28Al15Ni7,TRUE\nZr28Ti41Cu31,FALSE\nZr29Al11Ni60,TRUE\nZr29Al13Ni58,TRUE\nZr29Al33Ni38,TRUE\nZr29Al9Ni62,TRUE\nZr29Cu70B,TRUE\nZr29V10Ni11,TRUE\nZr2Al16Ni7,TRUE\nZr2Al17Ni6,TRUE\nZr2Al21Ni2,TRUE\nZr2Al2Ni,FALSE\nZr2Al3Ni5,FALSE\nZr2Al41Ni7,TRUE\nZr2Al43Ni5,TRUE\nZr2Al5Ni3,FALSE\nZr2Al7Ni,FALSE\nZr2Al83Ni15,FALSE\nZr2Al89Ni9,TRUE\nZr2AlCo17,TRUE\nZr2AlNi,TRUE\nZr2AlNi17,TRUE\nZr2AlNi2,TRUE\nZr2AlNi7,FALSE\nZr2Co13B5,TRUE\nZr2Co17B,TRUE\nZr2Co17Mo,TRUE\nZr2Co17Ni,TRUE\nZr2Co17Si,TRUE\nZr2Co17W,TRUE\nZr2Cr5Co13,TRUE\nZr2Cr5Fe13,TRUE\nZr2CrCo17,TRUE\nZr2Cu2Ni,TRUE\nZr2Cu3,TRUE\nZr2Cu3Ni5,FALSE\nZr2Cu5Ni3,FALSE\nZr2Cu7Ni,FALSE\nZr2CuNi,TRUE\nZr2CuNi2,TRUE\nZr2Fe17B,TRUE\nZr2Fe18B5,TRUE\nZr2Fe20B3,TRUE\nZr2Fe22B,TRUE\nZr2Fe23,TRUE\nZr2Fe83B15,TRUE\nZr2FeCo17,TRUE\nZr2FeCu2,TRUE\nZr2Mn17Co,TRUE\nZr2Ni3,TRUE\nZr2Ti3Cu5,TRUE\nZr2Ti3Ni5,TRUE\nZr2TiSi,TRUE\nZr2TiSi2,TRUE\nZr2V2Co21,TRUE\nZr2VCo17,TRUE\nZr2VCo22,TRUE\nZr2VNi2,TRUE\nZr3(Fe10B)2,TRUE\nZr30.1Nb30Cu39.9,TRUE\nZr30Ni17B3,TRUE\nZr30Ni19B,TRUE\nZr31(Ti3Si20)3,TRUE\nZr31Ti4Si15,TRUE\nZr32.3Nb25Cu42.7,TRUE\nZr32.5Cu65B2.5,TRUE\nZr33Al13Ni4,TRUE\nZr33Al35Ni32,TRUE\nZr33Nb10Cu57,TRUE\nZr33Ni67,TRUE\nZr33Ti12Si5,TRUE\nZr34.4Nb20Cu45.6,TRUE\nZr34Fe11Si5,TRUE\nZr35(Ni4P)3,TRUE\nZr35(SiNi4)3,TRUE\nZr35Al13Ni2,TRUE\nZr35Fe11B4,TRUE\nZr35Fe14Ir,TRUE\nZr35Fe14Pd,TRUE\nZr35Fe14Rh,TRUE\nZr35Fe14Ru,TRUE\nZr35Ti11Cu54,TRUE\nZr36.6Nb15Cu48.4,TRUE\nZr36Ti9Si55,TRUE\nZr37.5Cu55B7.5,TRUE\nZr37.5Cu60B2.5,TRUE\nZr37.5Sc37.5Fe25,TRUE\nZr37Al12Ni,TRUE\nZr37Ni12P,TRUE\nZr37Ni63,TRUE\nZr37SiNi12,TRUE\nZr38.7Nb10Cu51.3,TRUE\nZr38Al11Ni,TRUE\nZr38Nb5Cu57,TRUE\nZr38V25Ni37,TRUE\nZr39Al10Ni,TRUE\nZr39Al35Ni26,TRUE\nZr39Cu60B,TRUE\nZr39Ti11,TRUE\nZr39Ti26Si35,TRUE\nZr3Al,FALSE\nZr3Al11Ni6,FALSE\nZr3Al13Ni4,TRUE\nZr3Al14Ni3,FALSE\nZr3Al2Ni5,TRUE\nZr3Al38Ni9,TRUE\nZr3Al3Ni4,TRUE\nZr3Al42Ni5,TRUE\nZr3Al4Ni3,FALSE\nZr3Al5Ni2,FALSE\nZr3Al6Ni,FALSE\nZr3Al87Ni10,TRUE\nZr3AlNi,TRUE\nZr3AlNi6,TRUE\nZr3Be2,TRUE\nZr3BeNb,FALSE\nZr3Co15W2,TRUE\nZr3Co17,TRUE\nZr3Co41W6,TRUE\nZr3Co44Mo3,TRUE\nZr3Cr5Co42,TRUE\nZr3Cr6Co41,TRUE\nZr3Cr7Co40,TRUE\nZr3Cu2,TRUE\nZr3Cu2Ni5,TRUE\nZr3Cu3Ni4,TRUE\nZr3Cu4Ni3,TRUE\nZr3Cu5Ni2,TRUE\nZr3Cu6Ni,TRUE\nZr3Cu7,TRUE\nZr3CuNi,TRUE\nZr3CuNi6,TRUE\nZr3Fe15B2,TRUE\nZr3Fe16B,TRUE\nZr3Fe17,TRUE\nZr3Fe22,TRUE\nZr3Fe39B8,TRUE\nZr3Fe40B7,TRUE\nZr3Fe45B2,TRUE\nZr3Fe4Si13,TRUE\nZr3Fe75B22,TRUE\nZr3Fe78B19,TRUE\nZr3Fe80B17,TRUE\nZr3Fe82B15,TRUE\nZr3Fe87B10,TRUE\nZr3Fe90B7,FALSE\nZr3Fe93B4,FALSE\nZr3Nb13Si4,TRUE\nZr3Nb14Si3,TRUE\nZr3Nb5Si2,FALSE\nZr3Ni2,TRUE\nZr3Ni7,TRUE\nZr3Ti14Si3,TRUE\nZr3Ti22Si75,TRUE\nZr3Ti2Si5,TRUE\nZr3Ti3Be4,TRUE\nZr3Ti3Cu4,TRUE\nZr3Ti3Si14,TRUE\nZr3Ti4Cu13,TRUE\nZr3Ti4Si13,TRUE\nZr3Ti5Cu12,TRUE\nZr3Ti7Si40,TRUE\nZr3TiSi,TRUE\nZr3VNi6,TRUE\nZr4(AlNi)3,TRUE\nZr4(Co6Mo)3,TRUE\nZr4(CuNi)3,TRUE\nZr4(Fe25B7)3,TRUE\nZr4(Ti2Si5)3,TRUE\nZr4.5Fe92B3.5,TRUE\nZr40(FeCu19)3,TRUE\nZr40(Ti7Cu13)3,TRUE\nZr40.9Nb5Cu54.1,TRUE\nZr40Al9Ni,TRUE\nZr40Fe7Cu53,TRUE\nZr40FeCu59,TRUE\nZr40Ni59Pd,TRUE\nZr41Al7Ni2,TRUE\nZr41Ni9,TRUE\nZr42.5Cu50B7.5,TRUE\nZr42.5Cu55B2.5,TRUE\nZr42.6Nb1Cu56.4,TRUE\nZr42AlNi7,TRUE\nZr42NbCu57,TRUE\nZr43Nb40Si17,TRUE\nZr44Ti17Cu39,TRUE\nZr45(Al3Ni2)11,TRUE\nZr45Co54Pd,TRUE\nZr46.9Fe30Ni23.1,TRUE\nZr46.9Mn30Ni23.1,TRUE\nZr47.5Cu50B2.5,TRUE\nZr47Nb40Si13,TRUE\nZr47Ti8Si45,TRUE\nZr48Al25Ni27,TRUE\nZr49Cu50B,TRUE\nZr49Nb40Si11,TRUE\nZr49Ni49P2,TRUE\nZr4Al,FALSE\nZr4Al31Ni15,TRUE\nZr4Al33Ni13,TRUE\nZr4Al35Ni11,TRUE\nZr4Al41Ni5,FALSE\nZr4Al5Ni,FALSE\nZr4AlNi5,TRUE\nZr4Be,FALSE\nZr4Co17B4,TRUE\nZr4Co20W,TRUE\nZr4Co21,TRUE\nZr4Co45Mo,TRUE\nZr4CrNi5,TRUE\nZr4Cu5Ni,TRUE\nZr4CuNi5,TRUE\nZr4Fe35B11,TRUE\nZr4Fe39B7,TRUE\nZr4Fe41B5,TRUE\nZr4Fe45B,TRUE\nZr4FeCu5,TRUE\nZr4Ni,TRUE\nZr4Ti,TRUE\nZr4Ti11Si35,TRUE\nZr4Ti13Si3,TRUE\nZr4Ti3Si13,TRUE\nZr4Ti5Cu11,TRUE\nZr4VCo20,TRUE\nZr5(Al13Ni2)3,TRUE\nZr5(Co14W)3,TRUE\nZr5(CrFe14)3,TRUE\nZr5(Fe13B2)3,TRUE\nZr5(Fe14B)3,TRUE\nZr5(Fe2Co3)9,TRUE\nZr5(Fe2Ni3)9,TRUE\nZr5(Fe3Co2)9,TRUE\nZr5(Fe3Ni2)9,TRUE\nZr5(Fe4Co)9,TRUE\nZr5(Fe4Ni)9,TRUE\nZr5(FeCo4)9,TRUE\nZr5(FeNi4)9,TRUE\nZr5(Nb4Ge)3,TRUE\nZr5(Nb4Si)3,TRUE\nZr5(Ti4Si)3,TRUE\nZr5(TiSi14)3,FALSE\nZr5(TiSi4)3,TRUE\nZr5.2Co74.8Mo20,TRUE\nZr5.2Co84.8Mo10,TRUE\nZr5.2Co84.8W10,TRUE\nZr5.2Co86.8W8,TRUE\nZr5.5Co86.5Mo8,TRUE\nZr5.5Co88.5W6,TRUE\nZr5.5Fe80B14.5,TRUE\nZr5.5Fe92B2.5,TRUE\nZr50.25Fe25Ni24.75,TRUE\nZr50.25Mn25Ni24.75,TRUE\nZr50.25Ti25Ni24.75,TRUE\nZr50.25V25Ni24.75,TRUE\nZr51.2Al20Ni28.8,TRUE\nZr51Nb40Si9,TRUE\nZr51V20Ni29,TRUE\nZr51V25Ni24,TRUE\nZr52.5Cu45B2.5,TRUE\nZr53.2Fe16.8B30,TRUE\nZr53.6Co20Ni26.4,TRUE\nZr53.6Cr20Ni26.4,TRUE\nZr53.6Cu20Ni26.4,TRUE\nZr53.6Fe20Ni26.4,TRUE\nZr53.6Mn20Ni26.4,TRUE\nZr53.6Ti20Ni26.4,TRUE\nZr53.6V20Ni26.4,TRUE\nZr53Nb30Si17,TRUE\nZr53Nb40Si7,FALSE\nZr54.4Al15Ni30.6,TRUE\nZr56.95Co15Ni28.05,TRUE\nZr56.95Cr15Ni28.05,TRUE\nZr56.95Cu15Ni28.05,TRUE\nZr56.95Fe15Ni28.05,TRUE\nZr56.95Mn15Ni28.05,TRUE\nZr56.95Ti15Ni28.05,TRUE\nZr56.95V15Ni28.05,TRUE\nZr57.5Cu35B7.5,TRUE\nZr57.5Cu40B2.5,TRUE\nZr57.6Al10Ni32.4,TRUE\nZr57Fe18B25,TRUE\nZr57Nb30Si13,TRUE\nZr57Ti8Si35,TRUE\nZr59Cu40B,TRUE\nZr59Nb30Si11,FALSE\nZr5Al29Ni16,TRUE\nZr5Al2Ni3,TRUE\nZr5Al3Ni2,TRUE\nZr5Al4Ni,FALSE\nZr5Al79Ni16,TRUE\nZr5Al82Ni13,TRUE\nZr5Al86Ni9,TRUE\nZr5Al87.5Ni7.5,FALSE\nZr5Al88Ni7,TRUE\nZr5AlCo44,TRUE\nZr5AlNi4,TRUE\nZr5AlNi44,TRUE\nZr5Co37B8,TRUE\nZr5Co3Ni2,TRUE\nZr5Co43B2,TRUE\nZr5Co44B,TRUE\nZr5Co44Ni,TRUE\nZr5Co44Si,TRUE\nZr5Co77Mo18,TRUE\nZr5Co79Mo16,TRUE\nZr5Co81Mo14,TRUE\nZr5Co83Mo12,TRUE\nZr5Cr2Fe43,TRUE\nZr5Cr4Fe41,TRUE\nZr5CrFe44,TRUE\nZr5Cu14B,TRUE\nZr5Cu2Ni3,TRUE\nZr5Cu3Ni2,TRUE\nZr5Cu4Ni,TRUE\nZr5CuNi4,TRUE\nZr5Fe34B11,TRUE\nZr5Fe41B4,TRUE\nZr5Fe43B2,TRUE\nZr5Fe43Co2,TRUE\nZr5Fe44B,TRUE\nZr5Fe73B22,TRUE\nZr5Fe78B17,TRUE\nZr5Fe82B13,TRUE\nZr5Fe84B11,TRUE\nZr5Fe86B9,TRUE\nZr5Fe88B7,FALSE\nZr5Mn2Fe43,TRUE\nZr5Mn44Co,TRUE\nZr5Mn4Fe41,TRUE\nZr5MnFe44,TRUE\nZr5Nb11Si4,TRUE\nZr5Ni78B17,TRUE\nZr5Ti2Si13,TRUE\nZr5Ti2Si3,TRUE\nZr5Ti2Si43,FALSE\nZr5Ti4Cu11,TRUE\nZr5Ti4Si11,TRUE\nZr5Ti4Si41,FALSE\nZr5TiSi44,FALSE\nZr5V3Ni2,TRUE\nZr6(AlNi)7,TRUE\nZr6.2Co89.8W4,TRUE\nZr6.5Cr16Co77.5,TRUE\nZr6.5Cr8Co85.5,TRUE\nZr6.5Fe92B1.5,TRUE\nZr6.5V10Co83.5,TRUE\nZr6.5V12Co81.5,TRUE\nZr6.5V14Co79.5,TRUE\nZr6.8Cr6Co87.2,TRUE\nZr6.8V16Co77.2,TRUE\nZr60.3Co10Ni29.7,TRUE\nZr60.3Cr10Ni29.7,TRUE\nZr60.3Cu10Ni29.7,TRUE\nZr60.3Fe10Ni29.7,TRUE\nZr60.3Mn10Ni29.7,TRUE\nZr60.3Ti10Ni29.7,TRUE\nZr60.3V10Ni29.7,TRUE\nZr60.8Al5Ni34.2,TRUE\nZr61(Nb10Si3)3,FALSE\nZr61Fe19B20,TRUE\nZr62.5Be32.5Nb5,TRUE\nZr62.5Be35Nb2.5,TRUE\nZr62.5Cu30B7.5,TRUE\nZr62.5Cu35B2.5,TRUE\nZr63.5Be32.5Nb4,TRUE\nZr63.65Co5Ni31.35,TRUE\nZr63.65Cr5Ni31.35,TRUE\nZr63.65Cu5Ni31.35,TRUE\nZr63.65Fe5Ni31.35,TRUE\nZr63.65Mn5Ni31.35,TRUE\nZr63.65Ti5Ni31.35,TRUE\nZr63.65V5Ni31.35,TRUE\nZr63Al27Ni10,TRUE\nZr63Fe20B17,TRUE\nZr63Nb30Si7,FALSE\nZr64V5Ni31,TRUE\nZr65Al7.5Cu27.5,TRUE\nZr65Be32.5Nb2.5,TRUE\nZr65Co34Pd,TRUE\nZr66.85Co33Ni0.15,TRUE\nZr66.85Cr33Ni0.15,TRUE\nZr66.85Cu33Ni0.15,TRUE\nZr66.85Fe33Ni0.15,TRUE\nZr66.85Mn33Ni0.15,TRUE\nZr66.85Ti0.15Ni33,TRUE\nZr66.85V0.15Ni33,TRUE\nZr66.8Co33Ni0.2,TRUE\nZr66.8Cr33Ni0.2,TRUE\nZr66.8Cu33Ni0.2,TRUE\nZr66.8Fe33Ni0.2,TRUE\nZr66.8Mn33Ni0.2,TRUE\nZr66.8Ti0.2Ni33,TRUE\nZr66.8V0.2Ni33,TRUE\nZr66.95Co33Ni0.05,TRUE\nZr66.95Cr33Ni0.05,TRUE\nZr66.95Cu33Ni0.05,TRUE\nZr66.95Fe33Ni0.05,TRUE\nZr66.95Mn33Ni0.05,TRUE\nZr66.95Ti0.05Ni33,TRUE\nZr66.95V0.05Ni33,TRUE\nZr66.9Co33Ni0.1,TRUE\nZr66.9Cr33Ni0.1,TRUE\nZr66.9Cu33Ni0.1,TRUE\nZr66.9Fe33Ni0.1,TRUE\nZr66.9Mn33Ni0.1,TRUE\nZr66.9Ti0.1Ni33,TRUE\nZr66.9V0.1Ni33,TRUE\nZr67(Al9Ni2)3,TRUE\nZr67(Co2P)11,TRUE\nZr67(Fe7B4)3,TRUE\nZr67.5Be32.5,TRUE\nZr67.5Cu25B7.5,TRUE\nZr67.5Cu30B2.5,TRUE\nZr67Co28P5,TRUE\nZr67Co33,TRUE\nZr67Cu33,TRUE\nZr67Fe13.2Ni19.8,TRUE\nZr67Fe16.5Ni16.5,TRUE\nZr67Fe20.2Ni12.8,TRUE\nZr67Fe23.1Ni9.9,TRUE\nZr67Fe29.7Ni3.3,TRUE\nZr67Fe3.3Ni29.7,TRUE\nZr67Fe33,TRUE\nZr67Fe6.6Ni26.4,TRUE\nZr67Fe9.9Ni23.1,TRUE\nZr67Ni33,TRUE\nZr67Ti8Si25,TRUE\nZr69Cu30B,TRUE\nZr6Al37Ni7,TRUE\nZr6Al3Ni,FALSE\nZr6Al3Ni11,TRUE\nZr6Al5Ni9,TRUE\nZr6AlNi13,TRUE\nZr6AlNi3,TRUE\nZr6Cu13B,TRUE\nZr6Cu3B,TRUE\nZr6Cu3Ni,TRUE\nZr6CuNi3,TRUE\nZr6Fe39B5,TRUE\nZr6Fe79B15,TRUE\nZr6Ni3B,TRUE\nZr6Ti11Si3,TRUE\nZr6Ti3Si11,TRUE\nZr6Ti5Cu9,TRUE\nZr6Ti5Si9,TRUE\nZr6V5Ni9,TRUE\nZr6VNi3,TRUE\nZr7(Al2Ni7)2,TRUE\nZr7(Al4Ni5)2,TRUE\nZr7(AlNi2)6,TRUE\nZr7(Cr6Co25)3,TRUE\nZr7(Fe26B5)3,TRUE\nZr7(Fe27B4)3,TRUE\nZr7(Fe29B2)3,TRUE\nZr7(Fe30B)3,TRUE\nZr7(V6Co25)3,TRUE\nZr7.2Cr20Co72.8,TRUE\nZr7.4Co86.2Mo6.4,TRUE\nZr7.5Co79.5W13,TRUE\nZr7.5Cr4Co88.5,TRUE\nZr7.5V20Co72.5,TRUE\nZr7.5V6Co86.5,TRUE\nZr7.8Co90.2W2,TRUE\nZr71.4Fe22.6B6,TRUE\nZr71Ti9Si20,TRUE\nZr72.5Cu25B2.5,TRUE\nZr72Ti23Si5,TRUE\nZr73Fe23B4,TRUE\nZr75Ni24P,TRUE\nZr75SiNi24,TRUE\nZr76(Ti3Si5)3,TRUE\nZr77.5Cu15B7.5,FALSE\nZr77.5Cu20B2.5,TRUE\nZr79Cu20B,FALSE\nZr7Al2Cr,TRUE\nZr7Al2Ni,TRUE\nZr7Al2Ni11,TRUE\nZr7Al3,FALSE\nZr7Al35Ni8,TRUE\nZr7Al3Ni10,TRUE\nZr7Al4Ni9,TRUE\nZr7Al5Ni13,TRUE\nZr7Al5Ni8,TRUE\nZr7Al6Ni7,TRUE\nZr7Al73Ni20,TRUE\nZr7Al7Ni11,TRUE\nZr7Al83Ni10,TRUE\nZr7AlNi12,TRUE\nZr7AlNi2,TRUE\nZr7Be2Nb,FALSE\nZr7Be3,TRUE\nZr7Co3,TRUE\nZr7Co37W6,TRUE\nZr7Co39W4,TRUE\nZr7Co89Mo4,TRUE\nZr7Co91B2,TRUE\nZr7Cu12B,TRUE\nZr7Cu13,TRUE\nZr7Cu2Ni,TRUE\nZr7Cu3,TRUE\nZr7CuNi2,TRUE\nZr7Fe3,TRUE\nZr7Fe77B16,TRUE\nZr7Fe84.5B8.5,TRUE\nZr7Fe85B8,TRUE\nZr7Fe89B4,TRUE\nZr7Fe91B2,TRUE\nZr7Fe92B,TRUE\nZr7Fe93,FALSE\nZr7Nb10Ge3,TRUE\nZr7Nb10Si3,TRUE\nZr7Ni13,TRUE\nZr7Ni3,TRUE\nZr7Ti10Si3,TRUE\nZr7Ti2Si,TRUE\nZr7Ti3Cu10,TRUE\nZr7Ti3Si10,TRUE\nZr7Ti4Cu9,TRUE\nZr7Ti4Si9,TRUE\nZr7V10Co33,TRUE\nZr7V2Ni11,TRUE\nZr7V8Co85,TRUE\nZr8(AlNi3)3,TRUE\nZr8(Cr3Co11)3,TRUE\nZr8(CrNi3)3,TRUE\nZr8(Ti3Si)3,TRUE\nZr8(TiSi3)3,TRUE\nZr8(VCo13)3,TRUE\nZr8.3Cr2Co89.7,TRUE\nZr8.3Cr8.3Co83.4,TRUE\nZr8.5V2Co89.5,TRUE\nZr83Al11Ni6,TRUE\nZr83AlNi16,TRUE\nZr83Ge17,TRUE\nZr83Si17,TRUE\nZr83Ti12Si5,TRUE\nZr85(Si2Sn3)3,TRUE\nZr85(Si4C)3,FALSE\nZr85Al8Si7,TRUE\nZr87Ge13,TRUE\nZr87Si13,TRUE\nZr8Al5Ni7,TRUE\nZr8AlNi,TRUE\nZr8AlNi11,TRUE\nZr8Co37B5,TRUE\nZr8Co37Mo5,TRUE\nZr8Co41B,TRUE\nZr8Co41Mo,TRUE\nZr8Co41W,TRUE\nZr8CrNi11,TRUE\nZr8Cu11B,TRUE\nZr8CuNi,FALSE\nZr8Fe75B17,TRUE\nZr8Fe85B7,TRUE\nZr8Fe89.5B2.5,TRUE\nZr8FeCu11,TRUE\nZr8Ni17,TRUE\nZr8TiSi,TRUE\nZr8V5Ni12,TRUE\nZr8VCo41,TRUE\nZr9(Co11W2)7,TRUE\nZr9.2Cr9.6Co81.2,TRUE\nZr9.2V9Co81.8,TRUE\nZr9.4Co81.6Mo9,TRUE\nZr9.5Co85.5W5,TRUE\nZr92.5Be7.5,FALSE\nZr97.5Be2.5,FALSE\nZr9Al30Ni11,TRUE\nZr9Al31Ni10,TRUE\nZr9Al3Ni8,TRUE\nZr9Al4Ni7,TRUE\nZr9Al59Ni32,TRUE\nZr9Al5Ni6,TRUE\nZr9Al6Ni5,TRUE\nZr9Al7Ni4,TRUE\nZr9Al81Ni10,TRUE\nZr9Al9Ni2,TRUE\nZr9Al9Ni7,TRUE\nZr9AlNi10,TRUE\nZr9Be,FALSE\nZr9Co11,TRUE\nZr9Co82.4Mo8.6,TRUE\nZr9Co91,TRUE\nZr9Cu10B,TRUE\nZr9Cu6Ni5,TRUE\nZr9Cu7Ni4,TRUE\nZr9Cu8Ni3,TRUE\nZr9Fe90B,TRUE\nZr9Fe91,TRUE\nZr9Nb8Ge3,TRUE\nZr9Nb8Si3,TRUE\nZr9Ta8Si3,TRUE\nZr9Ti3Si8,TRUE\nZr9Ti4Si7,TRUE\nZr9Ti8Si3,TRUE\nZr9V2Ni9,TRUE\nZr9V8Si3,TRUE\nZrAl14Ni5,FALSE\nZrAl16Ni3,TRUE\nZrAl17Ni2,TRUE\nZrAl18Ni,FALSE\nZrAl2Ni7,FALSE\nZrAl3Ni,TRUE\nZrAl43Ni6,TRUE\nZrAl44Ni5,TRUE\nZrAl4Ni5,FALSE\nZrAl5Ni4,FALSE\nZrAl7Ni2,TRUE\nZrAl8Ni,FALSE\nZrAlNi3,FALSE\nZrAlNi8,FALSE\nZrBe,TRUE\nZrCo7B2,TRUE\nZrCo8B,TRUE\nZrCo8Mo,TRUE\nZrCo8Ni,TRUE\nZrCo8W,TRUE\nZrCo9,TRUE\nZrCr2Co7,TRUE\nZrCr2Fe7,TRUE\nZrCrCo8,TRUE\nZrCrFe8,TRUE\nZrCu,TRUE\nZrCu19,FALSE\nZrCu3,FALSE\nZrCu3Ni,FALSE\nZrCu4,FALSE\nZrCuNi3,FALSE\nZrFe14B5,TRUE\nZrFe15B4,TRUE\nZrFe16B3,TRUE\nZrFe17B2,TRUE\nZrFe18B,FALSE\nZrFe2Co7,TRUE\nZrFe40B9,TRUE\nZrFe44B5,FALSE\nZrFe45B4,FALSE\nZrFe4Co5,TRUE\nZrFe5Co4,TRUE\nZrFe7B2,TRUE\nZrFe7Co2,TRUE\nZrFe8B,TRUE\nZrFe8Co,TRUE\nZrFe9,TRUE\nZrFeCo8,TRUE\nZrMn8Co,TRUE\nZrMn9,TRUE\nZrNb15Si4,TRUE\nZrNb3Si,TRUE\nZrNb79Si20,TRUE\nZrNb7Si2,TRUE\nZrNbCo8,TRUE\nZrNi,TRUE\nZrNi9,TRUE\nZrTi16Si3,TRUE\nZrTi2Si7,TRUE\nZrTi3Si16,TRUE\nZrTi4Si15,TRUE\nZrTi5Be4,TRUE\nZrTi9,FALSE\nZrTiSi2,TRUE\nZrTiSi3,TRUE\nZrVCo8,TRUE\nZrVNi2,TRUE\n"
  },
  {
    "path": "dataset/matbench_glass/matbench_glass.json",
    "content": "[\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5(CrFe14)3\\n\",\n        \"output\": \" Yes, Zr5(CrFe14)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr11(Fe12B)3\\n\",\n        \"output\": \" No, Cr11(Fe12B)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10Cr17Fe73\\n\",\n        \"output\": \" Yes, Zr10Cr17Fe73 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf6Zr11Si3\\n\",\n        \"output\": \" Yes, Hf6Zr11Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti15Nb26Si9\\n\",\n        \"output\": \" Yes, Ti15Nb26Si9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg27Ti43Al30\\n\",\n        \"output\": \" No, Mg27Ti43Al30 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba7La65Cu28\\n\",\n        \"output\": \" Yes, Ba7La65Cu28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe80.5Ni2.5B17\\n\",\n        \"output\": \" Yes, Fe80.5Ni2.5B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf67Co33\\n\",\n        \"output\": \" Yes, Hf67Co33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni75P18W7\\n\",\n        \"output\": \" Yes, Ni75P18W7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5(Ni4P)19\\n\",\n        \"output\": \" Yes, Cr5(Ni4P)19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe80B13C7\\n\",\n        \"output\": \" Yes, Fe80B13C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2Al3\\n\",\n        \"output\": \" No, La2Al3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ga8Fe75B17\\n\",\n        \"output\": \" Yes, Ga8Fe75B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al14Ni\\n\",\n        \"output\": \" No, La5Al14Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al75Fe14Ni11\\n\",\n        \"output\": \" Yes, Al75Fe14Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al4Ni29B17\\n\",\n        \"output\": \" Yes, Al4Ni29B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Al14Ni3\\n\",\n        \"output\": \" Yes, Nd3Al14Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn0.5Al87.5Ni12\\n\",\n        \"output\": \" Yes, Mn0.5Al87.5Ni12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.8Co33Ni0.2\\n\",\n        \"output\": \" Yes, Zr66.8Co33Ni0.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr85(Si2Sn3)3\\n\",\n        \"output\": \" Yes, Zr85(Si2Sn3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Pd76Au7.5\\n\",\n        \"output\": \" Yes, Si16.5Pd76Au7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Tb67.5Al22.5B10\\n\",\n        \"output\": \" Yes, Tb67.5Al22.5B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CrFe17B2\\n\",\n        \"output\": \" No, CrFe17B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y5Mg43Mn2\\n\",\n        \"output\": \" Yes, Y5Mg43Mn2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe38(CuAg)31\\n\",\n        \"output\": \" Yes, Fe38(CuAg)31 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al12Co25B13\\n\",\n        \"output\": \" Yes, Al12Co25B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd10Al79Ni11\\n\",\n        \"output\": \" Yes, Nd10Al79Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" P19Pd81\\n\",\n        \"output\": \" Yes, P19Pd81 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr5Fe19B\\n\",\n        \"output\": \" No, Cr5Fe19B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce8Mn5Al87\\n\",\n        \"output\": \" No, Ce8Mn5Al87 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Co17Ni\\n\",\n        \"output\": \" Yes, Zr2Co17Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41W2C7\\n\",\n        \"output\": \" No, Fe41W2C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Be2Nb\\n\",\n        \"output\": \" No, Zr7Be2Nb does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe37W8C5\\n\",\n        \"output\": \" No, Fe37W8C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Al45Ni2\\n\",\n        \"output\": \" Yes, Nd3Al45Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La13Al73Ni14\\n\",\n        \"output\": \" Yes, La13Al73Ni14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3Al47\\n\",\n        \"output\": \" No, Ce3Al47 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co17(MoC)4\\n\",\n        \"output\": \" Yes, Co17(MoC)4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn17.4Al78.6Si4\\n\",\n        \"output\": \" No, Mn17.4Al78.6Si4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf81V4Si15\\n\",\n        \"output\": \" Yes, Hf81V4Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si18Pd75Au7\\n\",\n        \"output\": \" Yes, Si18Pd75Au7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si5(B2Mo13)3\\n\",\n        \"output\": \" Yes, Si5(B2Mo13)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce7Al83Cu10\\n\",\n        \"output\": \" Yes, Ce7Al83Cu10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La6Al13Ni\\n\",\n        \"output\": \" No, La6Al13Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu16.5Si16.5Pd67\\n\",\n        \"output\": \" Yes, Cu16.5Si16.5Pd67 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe21BMo3\\n\",\n        \"output\": \" No, Fe21BMo3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf3Cu5Ni2\\n\",\n        \"output\": \" Yes, Hf3Cu5Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr4(La23Cu9)3\\n\",\n        \"output\": \" Yes, Sr4(La23Cu9)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr50.25V25Ni24.75\\n\",\n        \"output\": \" Yes, Zr50.25V25Ni24.75 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Mg10Ni7\\n\",\n        \"output\": \" Yes, Nd3Mg10Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr(Ge2Pd9)9\\n\",\n        \"output\": \" Yes, Cr(Ge2Pd9)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu6Si16.5Pd77.5\\n\",\n        \"output\": \" Yes, Cu6Si16.5Pd77.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti15Si4Ni\\n\",\n        \"output\": \" No, Ti15Si4Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y15Mg84Cu\\n\",\n        \"output\": \" Yes, Y15Mg84Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe79(B2P)7\\n\",\n        \"output\": \" Yes, Fe79(B2P)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf66V19Si15\\n\",\n        \"output\": \" Yes, Hf66V19Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg13(Ti18Al11)3\\n\",\n        \"output\": \" Yes, Mg13(Ti18Al11)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr66.85Mn33Ni0.15\\n\",\n        \"output\": \" Yes, Zr66.85Mn33Ni0.15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb15Co73Ni12\\n\",\n        \"output\": \" Yes, Nb15Co73Ni12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr33Al13Ni4\\n\",\n        \"output\": \" Yes, Zr33Al13Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" SmAl15Ni4\\n\",\n        \"output\": \" No, SmAl15Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdAl24\\n\",\n        \"output\": \" No, NdAl24 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" asparagus\\n\",\n        \"output\": \" asparagus is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe77B15P8\\n\",\n        \"output\": \" Yes, Fe77B15P8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn9Fe74P17\\n\",\n        \"output\": \" Yes, Mn9Fe74P17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4CuNi5\\n\",\n        \"output\": \" Yes, Zr4CuNi5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd4Al7Cu39\\n\",\n        \"output\": \" No, Nd4Al7Cu39 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7.6Fe81.1B11.3\\n\",\n        \"output\": \" Yes, Nb7.6Fe81.1B11.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn(Al6Co)7\\n\",\n        \"output\": \" No, Mn(Al6Co)7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg2Cu\\n\",\n        \"output\": \" Yes, NdMg2Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce23Al64Fe13\\n\",\n        \"output\": \" No, Ce23Al64Fe13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf11(V2Si)3\\n\",\n        \"output\": \" Yes, Hf11(V2Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" FeNi3P\\n\",\n        \"output\": \" Yes, FeNi3P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni71B15P14\\n\",\n        \"output\": \" Yes, Ni71B15P14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al64Fe13Cu23\\n\",\n        \"output\": \" No, Al64Fe13Cu23 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79(B6C)3\\n\",\n        \"output\": \" Yes, Fe79(B6C)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf4(CuNi)3\\n\",\n        \"output\": \" Yes, Hf4(CuNi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn35Co49B16\\n\",\n        \"output\": \" Yes, Mn35Co49B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr15Fe79B6\\n\",\n        \"output\": \" No, Cr15Fe79B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg18Ti27Al55\\n\",\n        \"output\": \" No, Mg18Ti27Al55 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Al2Cu5\\n\",\n        \"output\": \" Yes, La3Al2Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu3Ni17P5\\n\",\n        \"output\": \" Yes, Cu3Ni17P5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaMg18Ni\\n\",\n        \"output\": \" No, LaMg18Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe4Cu15Ag31\\n\",\n        \"output\": \" No, Fe4Cu15Ag31 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al9Co\\n\",\n        \"output\": \" No, Al9Co does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2Mg2Cu\\n\",\n        \"output\": \" Yes, La2Mg2Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf3Cu4Ni3\\n\",\n        \"output\": \" Yes, Hf3Cu4Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" VFe8B\\n\",\n        \"output\": \" No, VFe8B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn16Co5B4\\n\",\n        \"output\": \" Yes, Mn16Co5B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf2.1Fe88.4O9.5\\n\",\n        \"output\": \" No, Hf2.1Fe88.4O9.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn35.6Co53.4B11\\n\",\n        \"output\": \" Yes, Mn35.6Co53.4B11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe35W8C7\\n\",\n        \"output\": \" No, Fe35W8C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co4C\\n\",\n        \"output\": \" No, Co4C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co13Si4B3\\n\",\n        \"output\": \" No, Co13Si4B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Fe15B2\\n\",\n        \"output\": \" No, Mn3Fe15B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y5Mg91Mn4\\n\",\n        \"output\": \" Yes, Y5Mg91Mn4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15.8Co78.2W6\\n\",\n        \"output\": \" Yes, Zr15.8Co78.2W6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti13Ni67P20\\n\",\n        \"output\": \" Yes, Ti13Ni67P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La11(Al2Cu)3\\n\",\n        \"output\": \" Yes, La11(Al2Cu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" chalk\\n\",\n        \"output\": \" chalk is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg70Cu29Au\\n\",\n        \"output\": \" Yes, Mg70Cu29Au has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd7Al43\\n\",\n        \"output\": \" Yes, Nd7Al43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce4Al5Cu41\\n\",\n        \"output\": \" Yes, Ce4Al5Cu41 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf14(NbSi)3\\n\",\n        \"output\": \" Yes, Hf14(NbSi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La15Al4Ni\\n\",\n        \"output\": \" Yes, La15Al4Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr4Al35Ni11\\n\",\n        \"output\": \" Yes, Zr4Al35Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co16WC3\\n\",\n        \"output\": \" No, Co16WC3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnFe15B4\\n\",\n        \"output\": \" Yes, MnFe15B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti20(Al3Ni7)3\\n\",\n        \"output\": \" Yes, Ti20(Al3Ni7)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd50.4Fe33.6B16\\n\",\n        \"output\": \" Yes, Nd50.4Fe33.6B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe77.5P7.5C15\\n\",\n        \"output\": \" Yes, Fe77.5P7.5C15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" kettle\\n\",\n        \"output\": \" kettle is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2Al17Ni\\n\",\n        \"output\": \" Yes, Y2Al17Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co11Mo9C5\\n\",\n        \"output\": \" Yes, Co11Mo9C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Co3Ni2\\n\",\n        \"output\": \" Yes, Zr5Co3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr5La67.5Cu27.5\\n\",\n        \"output\": \" Yes, Sr5La67.5Cu27.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Mg9Ni7\\n\",\n        \"output\": \" Yes, Nd4Mg9Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si18Ni69B13\\n\",\n        \"output\": \" No, Si18Ni69B13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10Cu7Ni3\\n\",\n        \"output\": \" Yes, Zr10Cu7Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce5Al44Cu\\n\",\n        \"output\": \" Yes, Ce5Al44Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg13Cu4\\n\",\n        \"output\": \" Yes, Nd3Mg13Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6(Ni3B)11\\n\",\n        \"output\": \" Yes, Al6(Ni3B)11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al47FeCo2\\n\",\n        \"output\": \" No, Al47FeCo2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Cr5Co42\\n\",\n        \"output\": \" Yes, Zr3Cr5Co42 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CrNi15P4\\n\",\n        \"output\": \" Yes, CrNi15P4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6Ti3Si11\\n\",\n        \"output\": \" Yes, Zr6Ti3Si11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf8CuNi\\n\",\n        \"output\": \" No, Hf8CuNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co77.5W15C7.5\\n\",\n        \"output\": \" No, Co77.5W15C7.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Ti3Si8\\n\",\n        \"output\": \" Yes, Zr9Ti3Si8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" yugoslavian\\n\",\n        \"output\": \" yugoslavian is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce5AlCu44\\n\",\n        \"output\": \" No, Ce5AlCu44 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe42Cu5B3\\n\",\n        \"output\": \" No, Fe42Cu5B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Cu37Ag60\\n\",\n        \"output\": \" No, Ce3Cu37Ag60 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr66.85V0.15Ni33\\n\",\n        \"output\": \" Yes, Zr66.85V0.15Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti29(Nb5Si2)3\\n\",\n        \"output\": \" No, Ti29(Nb5Si2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce7Nb10Al83\\n\",\n        \"output\": \" Yes, Ce7Nb10Al83 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co14B7C4\\n\",\n        \"output\": \" Yes, Co14B7C4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe42B33N25\\n\",\n        \"output\": \" Yes, Fe42B33N25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe44B5\\n\",\n        \"output\": \" No, ZrFe44B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Fe2B\\n\",\n        \"output\": \" Yes, Ti7Fe2B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu7Ni34P9\\n\",\n        \"output\": \" No, Cu7Ni34P9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.8Fe33Ni0.2\\n\",\n        \"output\": \" Yes, Zr66.8Fe33Ni0.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3MgNi\\n\",\n        \"output\": \" Yes, Nd3MgNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Al42Ni5\\n\",\n        \"output\": \" Yes, Ce3Al42Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co21(BC)2\\n\",\n        \"output\": \" No, Co21(BC)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Al21Ni20\\n\",\n        \"output\": \" Yes, La9Al21Ni20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co13Si3B4\\n\",\n        \"output\": \" Yes, Co13Si3B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe77.5Si5B17.5\\n\",\n        \"output\": \" Yes, Fe77.5Si5B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr23Ni34Mo43\\n\",\n        \"output\": \" Yes, Cr23Ni34Mo43 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr85(Fe2B3)3\\n\",\n        \"output\": \" Yes, Cr85(Fe2B3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al13Si4Ni3\\n\",\n        \"output\": \" Yes, Al13Si4Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr7(Co7C2)2\\n\",\n        \"output\": \" No, Cr7(Co7C2)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd15Fe77B8\\n\",\n        \"output\": \" Yes, Nd15Fe77B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co21B3C\\n\",\n        \"output\": \" No, Co21B3C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si9(Ge2Au11)7\\n\",\n        \"output\": \" Yes, Si9(Ge2Au11)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" FeB5Mo14\\n\",\n        \"output\": \" Yes, FeB5Mo14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y7.5Mg88.5Mn4\\n\",\n        \"output\": \" Yes, Y7.5Mg88.5Mn4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnFe3B\\n\",\n        \"output\": \" Yes, MnFe3B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co15Si3C2\\n\",\n        \"output\": \" No, Co15Si3C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr3Ge18Pd79\\n\",\n        \"output\": \" Yes, Cr3Ge18Pd79 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" reminder\\n\",\n        \"output\": \" reminder is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca7Cu3\\n\",\n        \"output\": \" Yes, Ca7Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co13W3C4\\n\",\n        \"output\": \" No, Co13W3C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr2Co18B5\\n\",\n        \"output\": \" Yes, Cr2Co18B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr50.25Mn25Ni24.75\\n\",\n        \"output\": \" Yes, Zr50.25Mn25Ni24.75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr21(AlNi)2\\n\",\n        \"output\": \" Yes, Zr21(AlNi)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe37Cu63\\n\",\n        \"output\": \" No, Fe37Cu63 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe82.5Si5B12.5\\n\",\n        \"output\": \" Yes, Fe82.5Si5B12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr14(AlNi3)9\\n\",\n        \"output\": \" Yes, Zr14(AlNi3)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79B10P11\\n\",\n        \"output\": \" Yes, Fe79B10P11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Co82.4Mo8.6\\n\",\n        \"output\": \" Yes, Zr9Co82.4Mo8.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe79(B2C)7\\n\",\n        \"output\": \" Yes, Fe79(B2C)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al43Ni4\\n\",\n        \"output\": \" Yes, Ce3Al43Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al4Cr\\n\",\n        \"output\": \" No, Al4Cr does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sm5Fe77B18\\n\",\n        \"output\": \" Yes, Sm5Fe77B18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr16Co71B13\\n\",\n        \"output\": \" Yes, Zr16Co71B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn9Fe31B10\\n\",\n        \"output\": \" Yes, Mn9Fe31B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Ti4Si41\\n\",\n        \"output\": \" No, Zr5Ti4Si41 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co35W8C7\\n\",\n        \"output\": \" Yes, Co35W8C7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd4AlCu45\\n\",\n        \"output\": \" No, Nd4AlCu45 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13Al4Cu3\\n\",\n        \"output\": \" Yes, Zr13Al4Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co31W10C9\\n\",\n        \"output\": \" No, Co31W10C9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd5Mg11Ni4\\n\",\n        \"output\": \" Yes, Nd5Mg11Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg3Ag\\n\",\n        \"output\": \" Yes, YMg3Ag has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg3Ti7Al15\\n\",\n        \"output\": \" Yes, Mg3Ti7Al15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al44Co3\\n\",\n        \"output\": \" No, Mn3Al44Co3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" FeCu9\\n\",\n        \"output\": \" No, FeCu9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7SiNi2\\n\",\n        \"output\": \" Yes, Ti7SiNi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd5(Mg4Cu)3\\n\",\n        \"output\": \" No, Nd5(Mg4Cu)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrMn8Co\\n\",\n        \"output\": \" Yes, ZrMn8Co has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La8AlCu\\n\",\n        \"output\": \" No, La8AlCu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf13Al2Ni5\\n\",\n        \"output\": \" Yes, Hf13Al2Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnAl48Co\\n\",\n        \"output\": \" No, MnAl48Co does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La13Al4Ni3\\n\",\n        \"output\": \" Yes, La13Al4Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd7Mg11Ni2\\n\",\n        \"output\": \" Yes, Nd7Mg11Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr53.6Cu20Ni26.4\\n\",\n        \"output\": \" Yes, Zr53.6Cu20Ni26.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrNb79Si20\\n\",\n        \"output\": \" Yes, ZrNb79Si20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl17Ni2\\n\",\n        \"output\": \" Yes, CeAl17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe83B8P9\\n\",\n        \"output\": \" Yes, Fe83B8P9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al13V2Cu5\\n\",\n        \"output\": \" Yes, Al13V2Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co9C\\n\",\n        \"output\": \" No, Co9C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.8Cr33Ni0.2\\n\",\n        \"output\": \" Yes, Zr66.8Cr33Ni0.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAl36Ni13\\n\",\n        \"output\": \" Yes, LaAl36Ni13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V5Fe87B8\\n\",\n        \"output\": \" No, V5Fe87B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaMg15Zn4\\n\",\n        \"output\": \" Yes, LaMg15Zn4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" face\\n\",\n        \"output\": \" face is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti9Al\\n\",\n        \"output\": \" No, Ti9Al does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf2(Zr5Si)3\\n\",\n        \"output\": \" Yes, Hf2(Zr5Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al22FeCo2\\n\",\n        \"output\": \" No, Al22FeCo2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti11(Nb2Si)3\\n\",\n        \"output\": \" Yes, Ti11(Nb2Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al4Fe39B7\\n\",\n        \"output\": \" Yes, Al4Fe39B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe37B4Mo9\\n\",\n        \"output\": \" No, Fe37B4Mo9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb76.5Si8.5Ge15\\n\",\n        \"output\": \" Yes, Nb76.5Si8.5Ge15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti9Ni11\\n\",\n        \"output\": \" No, Ti9Ni11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti5Al3Cu2\\n\",\n        \"output\": \" No, Ti5Al3Cu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al65Si17.5Ni17.5\\n\",\n        \"output\": \" Yes, Al65Si17.5Ni17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg9Ti44Al47\\n\",\n        \"output\": \" Yes, Mg9Ti44Al47 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl18Co\\n\",\n        \"output\": \" Yes, CeAl18Co has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb8.3Fe78.5B13.2\\n\",\n        \"output\": \" Yes, Nb8.3Fe78.5B13.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr56.95V15Ni28.05\\n\",\n        \"output\": \" Yes, Zr56.95V15Ni28.05 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti14Be5Si\\n\",\n        \"output\": \" Yes, Ti14Be5Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe40GeB9\\n\",\n        \"output\": \" Yes, Fe40GeB9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf2Cu5Ni3\\n\",\n        \"output\": \" Yes, Hf2Cu5Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al44FeCo5\\n\",\n        \"output\": \" No, Al44FeCo5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr12V15Ni23\\n\",\n        \"output\": \" Yes, Zr12V15Ni23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co10Si16.5Pd73.5\\n\",\n        \"output\": \" Yes, Co10Si16.5Pd73.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce10Mn7Al83\\n\",\n        \"output\": \" No, Ce10Mn7Al83 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf7Fe89B4\\n\",\n        \"output\": \" Yes, Hf7Fe89B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" methane\\n\",\n        \"output\": \" methane is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co17W3C5\\n\",\n        \"output\": \" No, Co17W3C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce(Cu7Ag5)2\\n\",\n        \"output\": \" Yes, Ce(Cu7Ag5)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe18B5W2\\n\",\n        \"output\": \" Yes, Fe18B5W2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Mg7Ni\\n\",\n        \"output\": \" No, Ce2Mg7Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Ti3Cu4\\n\",\n        \"output\": \" Yes, Zr3Ti3Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al43CoNi6\\n\",\n        \"output\": \" No, Al43CoNi6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" SiNi17C2\\n\",\n        \"output\": \" No, SiNi17C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4Al5Ni11\\n\",\n        \"output\": \" Yes, La4Al5Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeCu19Ag5\\n\",\n        \"output\": \" No, CeCu19Ag5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg10AlZn9\\n\",\n        \"output\": \" Yes, Mg10AlZn9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe82.5B17.5\\n\",\n        \"output\": \" Yes, Fe82.5B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3MgNi6\\n\",\n        \"output\": \" No, Nd3MgNi6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Al17Cr\\n\",\n        \"output\": \" Yes, Ce2Al17Cr has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti(Co3B)6\\n\",\n        \"output\": \" Yes, Ti(Co3B)6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Mg85Ni6\\n\",\n        \"output\": \" Yes, La9Mg85Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La37(Al19Ni2)3\\n\",\n        \"output\": \" Yes, La37(Al19Ni2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdAl15Ni4\\n\",\n        \"output\": \" No, NdAl15Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf3Cu3Ni4\\n\",\n        \"output\": \" Yes, Hf3Cu3Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Al31Ni10\\n\",\n        \"output\": \" Yes, Zr9Al31Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr19(Ni5Mo22)3\\n\",\n        \"output\": \" No, Cr19(Ni5Mo22)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al52Co23Si25\\n\",\n        \"output\": \" Yes, Al52Co23Si25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg20Al23Pd7\\n\",\n        \"output\": \" No, Mg20Al23Pd7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al85FeNi14\\n\",\n        \"output\": \" No, Al85FeNi14 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Mg12Cu5\\n\",\n        \"output\": \" No, Ce3Mg12Cu5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe61Co22B17\\n\",\n        \"output\": \" Yes, Fe61Co22B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr3Fe21B\\n\",\n        \"output\": \" No, Cr3Fe21B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" input\\n\",\n        \"output\": \" input is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" fragrance\\n\",\n        \"output\": \" fragrance is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co7Si3\\n\",\n        \"output\": \" No, Co7Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si7.5B20Mo72.5\\n\",\n        \"output\": \" Yes, Si7.5B20Mo72.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al17CrSi2\\n\",\n        \"output\": \" No, Al17CrSi2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe34W7C9\\n\",\n        \"output\": \" No, Fe34W7C9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti15Be2Si3\\n\",\n        \"output\": \" No, Ti15Be2Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe78Si7B15\\n\",\n        \"output\": \" Yes, Fe78Si7B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al21Ni2\\n\",\n        \"output\": \" No, Mn2Al21Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co13B7\\n\",\n        \"output\": \" Yes, Co13B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf3Cu2\\n\",\n        \"output\": \" Yes, Hf3Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co16B9\\n\",\n        \"output\": \" Yes, Co16B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni81.5B15P3.5\\n\",\n        \"output\": \" Yes, Ni81.5B15P3.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrCrFe8\\n\",\n        \"output\": \" Yes, ZrCrFe8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe12Ag13\\n\",\n        \"output\": \" No, Fe12Ag13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe84B5P11\\n\",\n        \"output\": \" No, Fe84B5P11 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si9Ni36B5\\n\",\n        \"output\": \" No, Si9Ni36B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79(BP2)7\\n\",\n        \"output\": \" Yes, Fe79(BP2)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl47Ni2\\n\",\n        \"output\": \" No, NdAl47Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe57Ni19B24\\n\",\n        \"output\": \" Yes, Fe57Ni19B24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf(CuNi)2\\n\",\n        \"output\": \" Yes, Hf(CuNi)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" V4(Fe25B7)3\\n\",\n        \"output\": \" Yes, V4(Fe25B7)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr53Nb40Si7\\n\",\n        \"output\": \" No, Zr53Nb40Si7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co67.5W17.5C15\\n\",\n        \"output\": \" No, Co67.5W17.5C15 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr14Cu5B\\n\",\n        \"output\": \" Yes, Zr14Cu5B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" norwegian\\n\",\n        \"output\": \" norwegian is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrMn9\\n\",\n        \"output\": \" Yes, ZrMn9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5.5Co88.5W6\\n\",\n        \"output\": \" Yes, Zr5.5Co88.5W6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2(Ni11B5)3\\n\",\n        \"output\": \" Yes, Al2(Ni11B5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" aquarius\\n\",\n        \"output\": \" aquarius is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La39Al2Ni59\\n\",\n        \"output\": \" Yes, La39Al2Ni59 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Be7Nb\\n\",\n        \"output\": \" Yes, Zr12Be7Nb has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr6Ni3B\\n\",\n        \"output\": \" Yes, Zr6Ni3B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79B20W\\n\",\n        \"output\": \" Yes, Fe79B20W has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni39B8C3\\n\",\n        \"output\": \" Yes, Ni39B8C3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe12B5F3\\n\",\n        \"output\": \" Yes, Fe12B5F3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ticket\\n\",\n        \"output\": \" ticket is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti6CuNi3\\n\",\n        \"output\": \" Yes, Ti6CuNi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7.2Cr20Co72.8\\n\",\n        \"output\": \" Yes, Zr7.2Cr20Co72.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca2.5Al87.5Ni10\\n\",\n        \"output\": \" No, Ca2.5Al87.5Ni10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co73Si13.5B13.5\\n\",\n        \"output\": \" Yes, Co73Si13.5B13.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NiPd4\\n\",\n        \"output\": \" Yes, NiPd4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn17.4Al66.6Si16\\n\",\n        \"output\": \" No, Mn17.4Al66.6Si16 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Cu14B\\n\",\n        \"output\": \" Yes, Zr5Cu14B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79(Cu5B2)3\\n\",\n        \"output\": \" No, Fe79(Cu5B2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.95Cu33Ni0.05\\n\",\n        \"output\": \" Yes, Zr66.95Cu33Ni0.05 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al7Cu3\\n\",\n        \"output\": \" No, Al7Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La9Cu36.4Au54.6\\n\",\n        \"output\": \" Yes, La9Cu36.4Au54.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2(Al15Ni)3\\n\",\n        \"output\": \" Yes, Nd2(Al15Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe89B6F5\\n\",\n        \"output\": \" No, Fe89B6F5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al34V5Ge11\\n\",\n        \"output\": \" Yes, Al34V5Ge11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2Al21Ni2\\n\",\n        \"output\": \" Yes, Nd2Al21Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co12.5Ni70.5P17\\n\",\n        \"output\": \" No, Co12.5Ni70.5P17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al6Ni27B17\\n\",\n        \"output\": \" Yes, Al6Ni27B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni69Mo12P19\\n\",\n        \"output\": \" Yes, Ni69Mo12P19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Al15Cu2\\n\",\n        \"output\": \" No, Ce3Al15Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr53.2Fe16.8B30\\n\",\n        \"output\": \" Yes, Zr53.2Fe16.8B30 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5P5C17.5\\n\",\n        \"output\": \" No, Fe77.5P5C17.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al45Co3Ni2\\n\",\n        \"output\": \" No, Al45Co3Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeMg3Ni\\n\",\n        \"output\": \" Yes, CeMg3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe8BP\\n\",\n        \"output\": \" Yes, Fe8BP has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr7NiP2\\n\",\n        \"output\": \" No, Cr7NiP2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15Al3Ni2\\n\",\n        \"output\": \" Yes, Zr15Al3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni35(B3C2)3\\n\",\n        \"output\": \" Yes, Ni35(B3C2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Mn2Fe43\\n\",\n        \"output\": \" Yes, Zr5Mn2Fe43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca6.5La56.5Cu37\\n\",\n        \"output\": \" Yes, Ca6.5La56.5Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83B3P14\\n\",\n        \"output\": \" No, Fe83B3P14 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti8NbSi\\n\",\n        \"output\": \" No, Ti8NbSi does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu5.9Si17.5Pd76.6\\n\",\n        \"output\": \" Yes, Cu5.9Si17.5Pd76.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl7Cu2\\n\",\n        \"output\": \" No, LaAl7Cu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca5(Mg3Cu2)3\\n\",\n        \"output\": \" Yes, Ca5(Mg3Cu2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CrSi20Pd79\\n\",\n        \"output\": \" Yes, CrSi20Pd79 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf68Nb17Si15\\n\",\n        \"output\": \" Yes, Hf68Nb17Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Fe82B15\\n\",\n        \"output\": \" Yes, Zr3Fe82B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg9\\n\",\n        \"output\": \" No, YMg9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr36Ti9Si55\\n\",\n        \"output\": \" Yes, Zr36Ti9Si55 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe41(B2P)3\\n\",\n        \"output\": \" Yes, Fe41(B2P)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni66.5B17Mo16.5\\n\",\n        \"output\": \" Yes, Ni66.5B17Mo16.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr5Fe37B8\\n\",\n        \"output\": \" Yes, Cr5Fe37B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La4MgNi5\\n\",\n        \"output\": \" No, La4MgNi5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" MnAl45Co4\\n\",\n        \"output\": \" No, MnAl45Co4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb2Ni3\\n\",\n        \"output\": \" Yes, Nb2Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrCr2Co7\\n\",\n        \"output\": \" Yes, ZrCr2Co7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co67.5Si12.5B20\\n\",\n        \"output\": \" Yes, Co67.5Si12.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd5(AlCu14)3\\n\",\n        \"output\": \" Yes, Nd5(AlCu14)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe35(W2C3)3\\n\",\n        \"output\": \" No, Fe35(W2C3)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al8Co29B13\\n\",\n        \"output\": \" Yes, Al8Co29B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr5Fe87B8\\n\",\n        \"output\": \" No, Cr5Fe87B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe7Co2\\n\",\n        \"output\": \" Yes, ZrFe7Co2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co14SiB5\\n\",\n        \"output\": \" Yes, Co14SiB5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Al6Ni\\n\",\n        \"output\": \" No, La3Al6Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd4Mg9Cu7\\n\",\n        \"output\": \" Yes, Nd4Mg9Cu7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti11Be7Si2\\n\",\n        \"output\": \" No, Ti11Be7Si2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr6Al37Ni7\\n\",\n        \"output\": \" Yes, Zr6Al37Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu6.1Si15.5Pd78.4\\n\",\n        \"output\": \" Yes, Cu6.1Si15.5Pd78.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co7Ni71P22\\n\",\n        \"output\": \" No, Co7Ni71P22 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La14(AlNi)3\\n\",\n        \"output\": \" Yes, La14(AlNi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Dy42Zr5Fe3\\n\",\n        \"output\": \" No, Dy42Zr5Fe3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti8AlCu\\n\",\n        \"output\": \" No, Ti8AlCu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn7(Co2B)6\\n\",\n        \"output\": \" Yes, Mn7(Co2B)6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr10Fe33B7\\n\",\n        \"output\": \" Yes, Cr10Fe33B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeCu24Ag25\\n\",\n        \"output\": \" No, CeCu24Ag25 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe32Cu37Ag31\\n\",\n        \"output\": \" No, Fe32Cu37Ag31 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti10Be9Si\\n\",\n        \"output\": \" No, Ti10Be9Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al2Fe41B7\\n\",\n        \"output\": \" Yes, Al2Fe41B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni18B6C\\n\",\n        \"output\": \" No, Ni18B6C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al14Ni25B11\\n\",\n        \"output\": \" No, Al14Ni25B11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce10Al77Co13\\n\",\n        \"output\": \" No, Ce10Al77Co13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn12Fe71P17\\n\",\n        \"output\": \" Yes, Mn12Fe71P17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu2(Ni13P3)3\\n\",\n        \"output\": \" Yes, Cu2(Ni13P3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al9V3Ge8\\n\",\n        \"output\": \" No, Al9V3Ge8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti16SiNi8\\n\",\n        \"output\": \" Yes, Ti16SiNi8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7Ti3Si10\\n\",\n        \"output\": \" Yes, Zr7Ti3Si10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti13V4Si3\\n\",\n        \"output\": \" Yes, Ti13V4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca2Mg17Zn\\n\",\n        \"output\": \" Yes, Ca2Mg17Zn has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnSi20Pd79\\n\",\n        \"output\": \" Yes, MnSi20Pd79 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe71B29\\n\",\n        \"output\": \" Yes, Fe71B29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al61(Cr7Si6)3\\n\",\n        \"output\": \" No, Al61(Cr7Si6)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti4Co35B11\\n\",\n        \"output\": \" Yes, Ti4Co35B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd5(Al14Ni)3\\n\",\n        \"output\": \" Yes, Gd5(Al14Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11Al57Ni32\\n\",\n        \"output\": \" Yes, Zr11Al57Ni32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80Ni3B17\\n\",\n        \"output\": \" Yes, Fe80Ni3B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co15SiB4\\n\",\n        \"output\": \" Yes, Co15SiB4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti12Si5Ni8\\n\",\n        \"output\": \" Yes, Ti12Si5Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al10Co33B7\\n\",\n        \"output\": \" No, Al10Co33B7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al43Fe3Co4\\n\",\n        \"output\": \" No, Al43Fe3Co4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5P12.5C10\\n\",\n        \"output\": \" Yes, Fe77.5P12.5C10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe87Ni5B8\\n\",\n        \"output\": \" No, Fe87Ni5B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83B2Mo15\\n\",\n        \"output\": \" No, Fe83B2Mo15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti5Cu2Ni3\\n\",\n        \"output\": \" Yes, Ti5Cu2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg22Ti67Al11\\n\",\n        \"output\": \" No, Mg22Ti67Al11 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Fe82B15\\n\",\n        \"output\": \" Yes, Nd3Fe82B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe41(BP2)3\\n\",\n        \"output\": \" Yes, Fe41(BP2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti5Be4Si\\n\",\n        \"output\": \" No, Ti5Be4Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg4Cu3\\n\",\n        \"output\": \" Yes, Y3Mg4Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg11Ti32Al57\\n\",\n        \"output\": \" Yes, Mg11Ti32Al57 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdMg13Cu6\\n\",\n        \"output\": \" Yes, NdMg13Cu6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.8Mn33Ni0.2\\n\",\n        \"output\": \" Yes, Zr66.8Mn33Ni0.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SiNi7C2\\n\",\n        \"output\": \" No, SiNi7C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr12Al3Ni5\\n\",\n        \"output\": \" Yes, Zr12Al3Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti8SiNi11\\n\",\n        \"output\": \" Yes, Ti8SiNi11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrAl18Ni\\n\",\n        \"output\": \" No, ZrAl18Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce6Al85Ni9\\n\",\n        \"output\": \" Yes, Ce6Al85Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al44Fe5Ni\\n\",\n        \"output\": \" No, Al44Fe5Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe82(BP)9\\n\",\n        \"output\": \" Yes, Fe82(BP)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si2(Ni5B)3\\n\",\n        \"output\": \" Yes, Si2(Ni5B)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe43BMo6\\n\",\n        \"output\": \" No, Fe43BMo6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr64V5Ni31\\n\",\n        \"output\": \" Yes, Zr64V5Ni31 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" V5Fe83B12\\n\",\n        \"output\": \" Yes, V5Fe83B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11(Ti2Si)3\\n\",\n        \"output\": \" Yes, Zr11(Ti2Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co17(BC)4\\n\",\n        \"output\": \" No, Co17(BC)4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La32Al53Ni15\\n\",\n        \"output\": \" Yes, La32Al53Ni15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd4Mg11Cu5\\n\",\n        \"output\": \" Yes, Nd4Mg11Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co67.5Si20C12.5\\n\",\n        \"output\": \" Yes, Co67.5Si20C12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe83Si4B13\\n\",\n        \"output\": \" Yes, Fe83Si4B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti9Al2Ni9\\n\",\n        \"output\": \" No, Ti9Al2Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl19\\n\",\n        \"output\": \" No, CeAl19 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti16Al47Ni37\\n\",\n        \"output\": \" Yes, Ti16Al47Ni37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd5Mg3Ni2\\n\",\n        \"output\": \" Yes, Nd5Mg3Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr49Nb40Si11\\n\",\n        \"output\": \" Yes, Zr49Nb40Si11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7Ni3\\n\",\n        \"output\": \" Yes, Zr7Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La11AlNi8\\n\",\n        \"output\": \" Yes, La11AlNi8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Pr36B5Au9\\n\",\n        \"output\": \" Yes, Pr36B5Au9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al2Ni29B19\\n\",\n        \"output\": \" Yes, Al2Ni29B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce(Mg2Ni)3\\n\",\n        \"output\": \" Yes, Ce(Mg2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe73Co10B17\\n\",\n        \"output\": \" Yes, Fe73Co10B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti5Al41Ni54\\n\",\n        \"output\": \" No, Ti5Al41Ni54 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti29Be21\\n\",\n        \"output\": \" No, Ti29Be21 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg17Ag2\\n\",\n        \"output\": \" No, YMg17Ag2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al6NiGe3\\n\",\n        \"output\": \" Yes, Al6NiGe3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al45FeCo4\\n\",\n        \"output\": \" No, Al45FeCo4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe3CoB\\n\",\n        \"output\": \" Yes, Fe3CoB has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CuSi2Pd7\\n\",\n        \"output\": \" Yes, CuSi2Pd7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Ag5.5Pd78\\n\",\n        \"output\": \" Yes, Si16.5Ag5.5Pd78 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr8Co13C4\\n\",\n        \"output\": \" No, Cr8Co13C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf2Cu2Ni\\n\",\n        \"output\": \" Yes, Hf2Cu2Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CrFe16B3\\n\",\n        \"output\": \" Yes, CrFe16B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr42.6Nb1Cu56.4\\n\",\n        \"output\": \" Yes, Zr42.6Nb1Cu56.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe72Si13B15\\n\",\n        \"output\": \" Yes, Fe72Si13B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdAl46Ni3\\n\",\n        \"output\": \" No, NdAl46Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co14Ni69P17\\n\",\n        \"output\": \" No, Co14Ni69P17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf74V11Si15\\n\",\n        \"output\": \" Yes, Hf74V11Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Fe84B11\\n\",\n        \"output\": \" Yes, Zr5Fe84B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7V2Si\\n\",\n        \"output\": \" No, Ti7V2Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg15Al3Zn2\\n\",\n        \"output\": \" No, Mg15Al3Zn2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37W4C9\\n\",\n        \"output\": \" No, Fe37W4C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5.2Co74.8Mo20\\n\",\n        \"output\": \" Yes, Zr5.2Co74.8Mo20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg3(Ti6Al5)2\\n\",\n        \"output\": \" Yes, Mg3(Ti6Al5)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta3Nb13Si4\\n\",\n        \"output\": \" No, Ta3Nb13Si4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al3CrSi\\n\",\n        \"output\": \" No, Al3CrSi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiAl9\\n\",\n        \"output\": \" No, TiAl9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce8Al87Cr5\\n\",\n        \"output\": \" No, Ce8Al87Cr5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr32.5Cu65B2.5\\n\",\n        \"output\": \" Yes, Zr32.5Cu65B2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb7Fe77B16\\n\",\n        \"output\": \" Yes, Nb7Fe77B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm3Al16Ni\\n\",\n        \"output\": \" Yes, Sm3Al16Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y3Mg16Ni\\n\",\n        \"output\": \" No, Y3Mg16Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al21Cr4\\n\",\n        \"output\": \" No, Al21Cr4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4Cu\\n\",\n        \"output\": \" No, Ti4Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni37P26Pd37\\n\",\n        \"output\": \" Yes, Ni37P26Pd37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80Si3B17\\n\",\n        \"output\": \" Yes, Fe80Si3B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf15Cu4Ni\\n\",\n        \"output\": \" No, Hf15Cu4Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrCu3\\n\",\n        \"output\": \" No, ZrCu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Al2Cu21\\n\",\n        \"output\": \" Yes, Ce2Al2Cu21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce5Al13Fe2\\n\",\n        \"output\": \" No, Ce5Al13Fe2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La7Ni3\\n\",\n        \"output\": \" Yes, La7Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La11Al4Ni5\\n\",\n        \"output\": \" Yes, La11Al4Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2MgCu2\\n\",\n        \"output\": \" No, Nd2MgCu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La11Al5Fe4\\n\",\n        \"output\": \" Yes, La11Al5Fe4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe75.5Co7.5B17\\n\",\n        \"output\": \" Yes, Fe75.5Co7.5B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr12Fe31B7\\n\",\n        \"output\": \" Yes, Cr12Fe31B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni81B14C5\\n\",\n        \"output\": \" Yes, Ni81B14C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf15.2Zr60.8Fe24\\n\",\n        \"output\": \" Yes, Hf15.2Zr60.8Fe24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La36Al53Ni11\\n\",\n        \"output\": \" Yes, La36Al53Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg16Ni3\\n\",\n        \"output\": \" Yes, YMg16Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti5Cu4Ni\\n\",\n        \"output\": \" Yes, Ti5Cu4Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CrNi3P\\n\",\n        \"output\": \" Yes, CrNi3P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti12Al5Cu8\\n\",\n        \"output\": \" Yes, Ti12Al5Cu8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu12Si15.5Pd72.5\\n\",\n        \"output\": \" Yes, Cu12Si15.5Pd72.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co36Mo5C9\\n\",\n        \"output\": \" Yes, Co36Mo5C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Al21Ni\\n\",\n        \"output\": \" Yes, Nd3Al21Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd12.375Fe70.125B17.5\\n\",\n        \"output\": \" Yes, Nd12.375Fe70.125B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe17W3C5\\n\",\n        \"output\": \" Yes, Fe17W3C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe7SiC2\\n\",\n        \"output\": \" Yes, Fe7SiC2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti15CuNi4\\n\",\n        \"output\": \" Yes, Ti15CuNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La12Mg5Ni8\\n\",\n        \"output\": \" Yes, La12Mg5Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" watch\\n\",\n        \"output\": \" watch is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y15Mg48Cu37\\n\",\n        \"output\": \" Yes, Y15Mg48Cu37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb39Si7Ge4\\n\",\n        \"output\": \" Yes, Nb39Si7Ge4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrCuNi3\\n\",\n        \"output\": \" No, ZrCuNi3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf7Fe85B8\\n\",\n        \"output\": \" Yes, Hf7Fe85B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" badger\\n\",\n        \"output\": \" badger is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdFe4\\n\",\n        \"output\": \" Yes, NdFe4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y2MgCu2\\n\",\n        \"output\": \" No, Y2MgCu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn15Fe73B12\\n\",\n        \"output\": \" No, Mn15Fe73B12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Cu3Ni4\\n\",\n        \"output\": \" Yes, Zr3Cu3Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" cafe\\n\",\n        \"output\": \" cafe is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" FeCu33Ag16\\n\",\n        \"output\": \" No, FeCu33Ag16 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83B12C5\\n\",\n        \"output\": \" Yes, Fe83B12C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10(Fe7Co3)9\\n\",\n        \"output\": \" Yes, Zr10(Fe7Co3)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y3Cu2\\n\",\n        \"output\": \" Yes, Y3Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe3Ni13B4\\n\",\n        \"output\": \" Yes, Fe3Ni13B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr14(AlFe)3\\n\",\n        \"output\": \" Yes, Zr14(AlFe)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si2B5Mo13\\n\",\n        \"output\": \" Yes, Si2B5Mo13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Cu6Ni\\n\",\n        \"output\": \" Yes, Zr3Cu6Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn27Co41B32\\n\",\n        \"output\": \" Yes, Mn27Co41B32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf15Cu2Ni3\\n\",\n        \"output\": \" Yes, Hf15Cu2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni15Mo7C3\\n\",\n        \"output\": \" No, Ni15Mo7C3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al86Fe5Ni9\\n\",\n        \"output\": \" No, Al86Fe5Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al6Ni37B7\\n\",\n        \"output\": \" No, Al6Ni37B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co35(W2C3)3\\n\",\n        \"output\": \" Yes, Co35(W2C3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce13Al85V2\\n\",\n        \"output\": \" No, Ce13Al85V2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe25Ni59B16\\n\",\n        \"output\": \" Yes, Fe25Ni59B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdMg8Ni\\n\",\n        \"output\": \" Yes, NdMg8Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg3Cu2\\n\",\n        \"output\": \" Yes, Mg3Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta4Ni15P\\n\",\n        \"output\": \" Yes, Ta4Ni15P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf40.9Nb5Cu54.1\\n\",\n        \"output\": \" Yes, Hf40.9Nb5Cu54.1 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si5Pd17Au3\\n\",\n        \"output\": \" Yes, Si5Pd17Au3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti19Al31Ni50\\n\",\n        \"output\": \" No, Ti19Al31Ni50 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl5Cu44\\n\",\n        \"output\": \" No, CeAl5Cu44 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe87B13\\n\",\n        \"output\": \" Yes, Fe87B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd3Al16Ni\\n\",\n        \"output\": \" No, Gd3Al16Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CaLa13Cu6\\n\",\n        \"output\": \" Yes, CaLa13Cu6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al57V18Ge25\\n\",\n        \"output\": \" Yes, Al57V18Ge25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg14Cu3\\n\",\n        \"output\": \" Yes, Nd3Mg14Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr29Al11Ni60\\n\",\n        \"output\": \" Yes, Zr29Al11Ni60 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" missile\\n\",\n        \"output\": \" missile is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf56Nb29Si15\\n\",\n        \"output\": \" Yes, Hf56Nb29Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr71.4Fe22.6B6\\n\",\n        \"output\": \" Yes, Zr71.4Fe22.6B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al4Ni25B21\\n\",\n        \"output\": \" Yes, Al4Ni25B21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8Al5Ni7\\n\",\n        \"output\": \" Yes, Zr8Al5Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg9Ti21Al20\\n\",\n        \"output\": \" Yes, Mg9Ti21Al20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn4(Nb5Co27)3\\n\",\n        \"output\": \" Yes, Mn4(Nb5Co27)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti37Ni63\\n\",\n        \"output\": \" Yes, Ti37Ni63 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe3NiB\\n\",\n        \"output\": \" Yes, Fe3NiB has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7Al2Cu\\n\",\n        \"output\": \" No, La7Al2Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CrFe19B5\\n\",\n        \"output\": \" Yes, CrFe19B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr66.95V0.05Ni33\\n\",\n        \"output\": \" Yes, Zr66.95V0.05Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al90Co7\\n\",\n        \"output\": \" Yes, Ce3Al90Co7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si21Pd75Au4\\n\",\n        \"output\": \" Yes, Si21Pd75Au4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe82(BC)9\\n\",\n        \"output\": \" Yes, Fe82(BC)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe71Ni25B4\\n\",\n        \"output\": \" No, Fe71Ni25B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" VFe39B10\\n\",\n        \"output\": \" Yes, VFe39B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5AlNi4\\n\",\n        \"output\": \" Yes, Zr5AlNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2TiSi\\n\",\n        \"output\": \" Yes, Zr2TiSi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" cloudy\\n\",\n        \"output\": \" cloudy is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La8Al5Cu7\\n\",\n        \"output\": \" Yes, La8Al5Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La11Al5Au4\\n\",\n        \"output\": \" Yes, La11Al5Au4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Fe82B13\\n\",\n        \"output\": \" Yes, Zr5Fe82B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al48FeNi\\n\",\n        \"output\": \" No, Al48FeNi does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y3Mg12Ag5\\n\",\n        \"output\": \" Yes, Y3Mg12Ag5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" creek\\n\",\n        \"output\": \" creek is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe43Ni5B2\\n\",\n        \"output\": \" No, Fe43Ni5B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2Al41Ni7\\n\",\n        \"output\": \" No, Mn2Al41Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd16.5Fe66B17.5\\n\",\n        \"output\": \" Yes, Nd16.5Fe66B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" FeNi15P4\\n\",\n        \"output\": \" Yes, FeNi15P4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf78Nb7Si15\\n\",\n        \"output\": \" Yes, Hf78Nb7Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co36W5C9\\n\",\n        \"output\": \" No, Co36W5C9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe72.5Si15B12.5\\n\",\n        \"output\": \" Yes, Fe72.5Si15B12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf13V4Si3\\n\",\n        \"output\": \" Yes, Hf13V4Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg89Al9Ga2\\n\",\n        \"output\": \" No, Mg89Al9Ga2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La22AlNi27\\n\",\n        \"output\": \" Yes, La22AlNi27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn3Al12Si5\\n\",\n        \"output\": \" Yes, Mn3Al12Si5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd9Al83Ni8\\n\",\n        \"output\": \" Yes, Gd9Al83Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" FeCo3B\\n\",\n        \"output\": \" Yes, FeCo3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4Ti13Si3\\n\",\n        \"output\": \" Yes, Zr4Ti13Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe37Cu5B8\\n\",\n        \"output\": \" No, Fe37Cu5B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Nb4Ge3\\n\",\n        \"output\": \" Yes, Zr13Nb4Ge3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co59B41\\n\",\n        \"output\": \" Yes, Co59B41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeCu29Ag20\\n\",\n        \"output\": \" No, CeCu29Ag20 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al17V2Cu\\n\",\n        \"output\": \" Yes, Al17V2Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Al5Ni3\\n\",\n        \"output\": \" No, Zr2Al5Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15Fe2Si3\\n\",\n        \"output\": \" Yes, Zr15Fe2Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co34W7C9\\n\",\n        \"output\": \" No, Co34W7C9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15Al7Ni3\\n\",\n        \"output\": \" Yes, Zr15Al7Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al6Cr3Si\\n\",\n        \"output\": \" No, Al6Cr3Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41B8F\\n\",\n        \"output\": \" Yes, Fe41B8F has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdMg3Ni\\n\",\n        \"output\": \" Yes, NdMg3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3SiNi\\n\",\n        \"output\": \" No, Ti3SiNi does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co23Mo20C7\\n\",\n        \"output\": \" No, Co23Mo20C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" shorts\\n\",\n        \"output\": \" shorts is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8CrSi\\n\",\n        \"output\": \" No, Al8CrSi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Nb6Si\\n\",\n        \"output\": \" No, Zr13Nb6Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe19B\\n\",\n        \"output\": \" No, Fe19B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y2Mg5Ni3\\n\",\n        \"output\": \" Yes, Y2Mg5Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Cu2Ni\\n\",\n        \"output\": \" Yes, Zr2Cu2Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79(B4C3)3\\n\",\n        \"output\": \" Yes, Fe79(B4C3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe3Ag7\\n\",\n        \"output\": \" No, Fe3Ag7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti32Al59Ni9\\n\",\n        \"output\": \" Yes, Ti32Al59Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" GdAl8Fe\\n\",\n        \"output\": \" Yes, GdAl8Fe has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe77.5Si2.5B20\\n\",\n        \"output\": \" Yes, Fe77.5Si2.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TaNi\\n\",\n        \"output\": \" Yes, TaNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Ni2\\n\",\n        \"output\": \" Yes, Nd3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al85(Ni4Mo)3\\n\",\n        \"output\": \" Yes, Al85(Ni4Mo)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti27Nb15Si8\\n\",\n        \"output\": \" Yes, Ti27Nb15Si8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca1.25Al88.75Ni10\\n\",\n        \"output\": \" No, Ca1.25Al88.75Ni10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" TaNbNi3\\n\",\n        \"output\": \" Yes, TaNbNi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe3NiP\\n\",\n        \"output\": \" Yes, Fe3NiP has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg19Zn\\n\",\n        \"output\": \" No, Mg19Zn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr5Fe41B4\\n\",\n        \"output\": \" Yes, Cr5Fe41B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti4Al7Cu9\\n\",\n        \"output\": \" No, Ti4Al7Cu9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al18CrSi\\n\",\n        \"output\": \" No, Al18CrSi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" GdAl9\\n\",\n        \"output\": \" Yes, GdAl9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co65Si22.5C12.5\\n\",\n        \"output\": \" Yes, Co65Si22.5C12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al2Ni37B11\\n\",\n        \"output\": \" Yes, Al2Ni37B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La26Al15Ni59\\n\",\n        \"output\": \" Yes, La26Al15Ni59 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Mg2Cu5\\n\",\n        \"output\": \" No, La3Mg2Cu5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si18Pd81Au\\n\",\n        \"output\": \" Yes, Si18Pd81Au has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr92.5Be7.5\\n\",\n        \"output\": \" No, Zr92.5Be7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La13Al77Ni10\\n\",\n        \"output\": \" Yes, La13Al77Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce4Al15Fe\\n\",\n        \"output\": \" No, Ce4Al15Fe does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb7Fe85B8\\n\",\n        \"output\": \" Yes, Nb7Fe85B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr39Al35Ni26\\n\",\n        \"output\": \" Yes, Zr39Al35Ni26 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co16Mo5C4\\n\",\n        \"output\": \" Yes, Co16Mo5C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La6(AlNi)7\\n\",\n        \"output\": \" Yes, La6(AlNi)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni4P\\n\",\n        \"output\": \" Yes, Ni4P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni2P5Pd18\\n\",\n        \"output\": \" Yes, Ni2P5Pd18 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni39B10C\\n\",\n        \"output\": \" Yes, Ni39B10C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni4P5Pt16\\n\",\n        \"output\": \" Yes, Ni4P5Pt16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5(TiSi4)3\\n\",\n        \"output\": \" Yes, Zr5(TiSi4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11Be9\\n\",\n        \"output\": \" Yes, Zr11Be9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al32Ni5Ge13\\n\",\n        \"output\": \" Yes, Al32Ni5Ge13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti13Be4Si3\\n\",\n        \"output\": \" No, Ti13Be4Si3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni17(MoC)4\\n\",\n        \"output\": \" No, Ni17(MoC)4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd(Al6Ni)7\\n\",\n        \"output\": \" Yes, Nd(Al6Ni)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al85Fe8Si7\\n\",\n        \"output\": \" No, Al85Fe8Si7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ni6.7Pd76.8\\n\",\n        \"output\": \" Yes, Si16.5Ni6.7Pd76.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti5Al2Cu3\\n\",\n        \"output\": \" Yes, Ti5Al2Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15.7V8Co76.3\\n\",\n        \"output\": \" Yes, Zr15.7V8Co76.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe85(NiB4)3\\n\",\n        \"output\": \" No, Fe85(NiB4)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn4Fe77B19\\n\",\n        \"output\": \" Yes, Mn4Fe77B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMgAg3\\n\",\n        \"output\": \" No, YMgAg3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf74Nb11Si15\\n\",\n        \"output\": \" Yes, Hf74Nb11Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Al8Ni3\\n\",\n        \"output\": \" Yes, La9Al8Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" cuticle\\n\",\n        \"output\": \" cuticle is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al45FeNi4\\n\",\n        \"output\": \" No, Al45FeNi4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrAl2Ni7\\n\",\n        \"output\": \" No, ZrAl2Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al5Fe2Cu3\\n\",\n        \"output\": \" No, Al5Fe2Cu3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2Mg2Cu\\n\",\n        \"output\": \" No, Nd2Mg2Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co37B13\\n\",\n        \"output\": \" Yes, Co37B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al10Fe23B17\\n\",\n        \"output\": \" Yes, Al10Fe23B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr63.65Mn5Ni31.35\\n\",\n        \"output\": \" Yes, Zr63.65Mn5Ni31.35 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni3B2\\n\",\n        \"output\": \" Yes, Ni3B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Cr7Fe83\\n\",\n        \"output\": \" Yes, Zr10Cr7Fe83 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Fe14B3\\n\",\n        \"output\": \" Yes, Nd3Fe14B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe16SiP3\\n\",\n        \"output\": \" Yes, Fe16SiP3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe20B4P\\n\",\n        \"output\": \" Yes, Fe20B4P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2Al5Cu3\\n\",\n        \"output\": \" No, La2Al5Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Co5B3\\n\",\n        \"output\": \" Yes, Al2Co5B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg14Ni3\\n\",\n        \"output\": \" Yes, Nd3Mg14Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Mg16Ni\\n\",\n        \"output\": \" No, Nd3Mg16Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd2(Al5Ni)3\\n\",\n        \"output\": \" Yes, Gd2(Al5Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Mg13Cu5\\n\",\n        \"output\": \" Yes, Nd2Mg13Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr30.1Nb30Cu39.9\\n\",\n        \"output\": \" Yes, Zr30.1Nb30Cu39.9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La24Al17Ni59\\n\",\n        \"output\": \" Yes, La24Al17Ni59 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" V15Co72.25B12.75\\n\",\n        \"output\": \" Yes, V15Co72.25B12.75 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" coach\\n\",\n        \"output\": \" coach is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2(AlCu15)3\\n\",\n        \"output\": \" No, Ce2(AlCu15)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb3(Fe10B)2\\n\",\n        \"output\": \" Yes, Nb3(Fe10B)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La11(AlNi2)3\\n\",\n        \"output\": \" Yes, La11(AlNi2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CrCo7B2\\n\",\n        \"output\": \" Yes, CrCo7B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Al15Ni7\\n\",\n        \"output\": \" Yes, La3Al15Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiCuNi8\\n\",\n        \"output\": \" No, TiCuNi8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Ti2Si13\\n\",\n        \"output\": \" Yes, Zr5Ti2Si13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Nb10Ge3\\n\",\n        \"output\": \" Yes, Zr7Nb10Ge3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al12Ni27B11\\n\",\n        \"output\": \" No, Al12Ni27B11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr9Fe36B5\\n\",\n        \"output\": \" No, Cr9Fe36B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Co17\\n\",\n        \"output\": \" Yes, Zr3Co17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2.5Fe80.5B17\\n\",\n        \"output\": \" Yes, Mn2.5Fe80.5B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni38(B3C)3\\n\",\n        \"output\": \" No, Ni38(B3C)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn9Co35B6\\n\",\n        \"output\": \" Yes, Mn9Co35B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe73(Ni5B4)3\\n\",\n        \"output\": \" Yes, Fe73(Ni5B4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Al6Ni5\\n\",\n        \"output\": \" Yes, Zr9Al6Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiAl4Cu5\\n\",\n        \"output\": \" Yes, TiAl4Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y9Al91\\n\",\n        \"output\": \" Yes, Y9Al91 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni29(Mo2C)7\\n\",\n        \"output\": \" No, Ni29(Mo2C)7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Ni31B17\\n\",\n        \"output\": \" Yes, Al2Ni31B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe85B7Mo8\\n\",\n        \"output\": \" No, Fe85B7Mo8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8(AlNi3)3\\n\",\n        \"output\": \" Yes, Zr8(AlNi3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr63Fe20B17\\n\",\n        \"output\": \" Yes, Zr63Fe20B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe82B7P11\\n\",\n        \"output\": \" Yes, Fe82B7P11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe81.5Cu0.5B18\\n\",\n        \"output\": \" Yes, Fe81.5Cu0.5B18 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2CrCo17\\n\",\n        \"output\": \" Yes, Zr2CrCo17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni4C\\n\",\n        \"output\": \" No, Ni4C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn25Co47B28\\n\",\n        \"output\": \" Yes, Mn25Co47B28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9Ti8Si3\\n\",\n        \"output\": \" Yes, Zr9Ti8Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg9Ti28Al13\\n\",\n        \"output\": \" Yes, Mg9Ti28Al13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Fe7\\n\",\n        \"output\": \" Yes, Nd3Fe7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf71Nb14Si15\\n\",\n        \"output\": \" Yes, Hf71Nb14Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr83Ge17\\n\",\n        \"output\": \" Yes, Zr83Ge17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mo3Ru2\\n\",\n        \"output\": \" Yes, Mo3Ru2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co33Mo8C9\\n\",\n        \"output\": \" Yes, Co33Mo8C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf10Cu7Ni3\\n\",\n        \"output\": \" Yes, Hf10Cu7Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe67.5Si15B17.5\\n\",\n        \"output\": \" Yes, Fe67.5Si15B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr60.3Cr10Ni29.7\\n\",\n        \"output\": \" Yes, Zr60.3Cr10Ni29.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe65Si17.5C17.5\\n\",\n        \"output\": \" Yes, Fe65Si17.5C17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiCu3\\n\",\n        \"output\": \" Yes, TiCu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5Mg83Ni12\\n\",\n        \"output\": \" Yes, Nd5Mg83Ni12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf67(V6Si5)3\\n\",\n        \"output\": \" Yes, Hf67(V6Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrFe8B\\n\",\n        \"output\": \" Yes, ZrFe8B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al47Fe3\\n\",\n        \"output\": \" No, Al47Fe3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti17(Al9Ni2)3\\n\",\n        \"output\": \" Yes, Ti17(Al9Ni2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn8.4Co75.6B16\\n\",\n        \"output\": \" Yes, Mn8.4Co75.6B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2Al16Ni7\\n\",\n        \"output\": \" Yes, La2Al16Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe72.5Si7.5B20\\n\",\n        \"output\": \" Yes, Fe72.5Si7.5B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La5Al3Cu2\\n\",\n        \"output\": \" Yes, La5Al3Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3TiSi\\n\",\n        \"output\": \" Yes, Zr3TiSi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe20.5Ni60.5B19\\n\",\n        \"output\": \" Yes, Fe20.5Ni60.5B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr13Co6Pd\\n\",\n        \"output\": \" Yes, Zr13Co6Pd has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe4P\\n\",\n        \"output\": \" Yes, Fe4P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe71B14Mo15\\n\",\n        \"output\": \" Yes, Fe71B14Mo15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAl49\\n\",\n        \"output\": \" No, MnAl49 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al88FeNi11\\n\",\n        \"output\": \" Yes, Al88FeNi11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni3PPd\\n\",\n        \"output\": \" Yes, Ni3PPd has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe3Co5B2\\n\",\n        \"output\": \" Yes, Fe3Co5B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si5Ni38B7\\n\",\n        \"output\": \" Yes, Si5Ni38B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrNb15Si4\\n\",\n        \"output\": \" Yes, ZrNb15Si4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Cu3Ni5\\n\",\n        \"output\": \" No, Ti2Cu3Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf13Nb4Si3\\n\",\n        \"output\": \" Yes, Hf13Nb4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd(MgCu2)3\\n\",\n        \"output\": \" No, Nd(MgCu2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Ti2Si43\\n\",\n        \"output\": \" No, Zr5Ti2Si43 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb40(Ni19Pt)3\\n\",\n        \"output\": \" Yes, Nb40(Ni19Pt)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La13AlNi6\\n\",\n        \"output\": \" Yes, La13AlNi6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni68.5B17Mo14.5\\n\",\n        \"output\": \" Yes, Ni68.5B17Mo14.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca12Mg7Ga\\n\",\n        \"output\": \" Yes, Ca12Mg7Ga has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SiNi36B13\\n\",\n        \"output\": \" Yes, SiNi36B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2Al47Ni\\n\",\n        \"output\": \" No, Nd2Al47Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnFe85B14\\n\",\n        \"output\": \" Yes, MnFe85B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn37(Co13B8)3\\n\",\n        \"output\": \" Yes, Mn37(Co13B8)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe89Ni5B6\\n\",\n        \"output\": \" No, Fe89Ni5B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti2AlNi7\\n\",\n        \"output\": \" No, Ti2AlNi7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al8Ni7\\n\",\n        \"output\": \" Yes, La5Al8Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce7Al83Fe10\\n\",\n        \"output\": \" Yes, Ce7Al83Fe10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb40Ni59Pd\\n\",\n        \"output\": \" Yes, Nb40Ni59Pd has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sr17La47Cu36\\n\",\n        \"output\": \" Yes, Sr17La47Cu36 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe41B4P5\\n\",\n        \"output\": \" Yes, Fe41B4P5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe40.5Ni40B19.5\\n\",\n        \"output\": \" Yes, Fe40.5Ni40B19.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5MnFe44\\n\",\n        \"output\": \" Yes, Zr5MnFe44 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B7P12\\n\",\n        \"output\": \" Yes, Fe81B7P12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13V4Ge3\\n\",\n        \"output\": \" Yes, Zr13V4Ge3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Mg4Cu3\\n\",\n        \"output\": \" Yes, La3Mg4Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf23Nb20Cu57\\n\",\n        \"output\": \" Yes, Hf23Nb20Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr10Ni4Mo11\\n\",\n        \"output\": \" Yes, Cr10Ni4Mo11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87V5Cu8\\n\",\n        \"output\": \" No, Al87V5Cu8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2(Ti5Si)3\\n\",\n        \"output\": \" Yes, Zr2(Ti5Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAl7Ni2\\n\",\n        \"output\": \" Yes, CeAl7Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6Co9B10\\n\",\n        \"output\": \" Yes, Al6Co9B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co31Mo8C11\\n\",\n        \"output\": \" Yes, Co31Mo8C11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr65Co34Pd\\n\",\n        \"output\": \" Yes, Zr65Co34Pd has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al49Fe\\n\",\n        \"output\": \" No, Al49Fe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn7.6Co68.4B24\\n\",\n        \"output\": \" Yes, Mn7.6Co68.4B24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrCu19\\n\",\n        \"output\": \" No, ZrCu19 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg14Ni3\\n\",\n        \"output\": \" Yes, La3Mg14Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Be5Nb3\\n\",\n        \"output\": \" No, Zr12Be5Nb3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y9(Mg5Cu3)2\\n\",\n        \"output\": \" Yes, Y9(Mg5Cu3)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La7Al7Ni6\\n\",\n        \"output\": \" Yes, La7Al7Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La6Al3Cu\\n\",\n        \"output\": \" Yes, La6Al3Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr66.8Ti0.2Ni33\\n\",\n        \"output\": \" Yes, Zr66.8Ti0.2Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg5Ni4\\n\",\n        \"output\": \" No, NdMg5Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15.7Co70.3Mo14\\n\",\n        \"output\": \" Yes, Zr15.7Co70.3Mo14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni19B\\n\",\n        \"output\": \" No, Ni19B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Cr7Co40\\n\",\n        \"output\": \" Yes, Zr3Cr7Co40 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg9\\n\",\n        \"output\": \" No, CeMg9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B19\\n\",\n        \"output\": \" Yes, Fe81B19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni27B17C6\\n\",\n        \"output\": \" Yes, Ni27B17C6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu85.2Ag7.1P7.7\\n\",\n        \"output\": \" Yes, Cu85.2Ag7.1P7.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr37.5Sc37.5Fe25\\n\",\n        \"output\": \" Yes, Zr37.5Sc37.5Fe25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La21Al28Ni\\n\",\n        \"output\": \" Yes, La21Al28Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7V8Co85\\n\",\n        \"output\": \" Yes, Zr7V8Co85 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti14(BeSi)3\\n\",\n        \"output\": \" No, Ti14(BeSi)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2Mg13Cu5\\n\",\n        \"output\": \" Yes, Y2Mg13Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10.8Cr11.2Co78\\n\",\n        \"output\": \" Yes, Zr10.8Cr11.2Co78 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al45Co4Ni\\n\",\n        \"output\": \" No, Al45Co4Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr4VCo20\\n\",\n        \"output\": \" Yes, Zr4VCo20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al7VGe2\\n\",\n        \"output\": \" No, Al7VGe2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta40Ni59Pd\\n\",\n        \"output\": \" Yes, Ta40Ni59Pd has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3Mg16Cu\\n\",\n        \"output\": \" No, Ce3Mg16Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr53.6V20Ni26.4\\n\",\n        \"output\": \" Yes, Zr53.6V20Ni26.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrAl43Ni6\\n\",\n        \"output\": \" Yes, ZrAl43Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe36.5Ni36.5B27\\n\",\n        \"output\": \" Yes, Fe36.5Ni36.5B27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co17W2C\\n\",\n        \"output\": \" No, Co17W2C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd21Fe21B8\\n\",\n        \"output\": \" Yes, Nd21Fe21B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co35(Mo2C3)3\\n\",\n        \"output\": \" Yes, Co35(Mo2C3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3AlCu6\\n\",\n        \"output\": \" No, La3AlCu6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr6.8Cr6Co87.2\\n\",\n        \"output\": \" Yes, Zr6.8Cr6Co87.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co10Ni68.5P21.5\\n\",\n        \"output\": \" No, Co10Ni68.5P21.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrAl7Ni2\\n\",\n        \"output\": \" Yes, ZrAl7Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu3.5Si16.5Pd80\\n\",\n        \"output\": \" Yes, Cu3.5Si16.5Pd80 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdMg19\\n\",\n        \"output\": \" No, NdMg19 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Al44Ni3\\n\",\n        \"output\": \" No, Mn3Al44Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe30.5Ni50.5B19\\n\",\n        \"output\": \" Yes, Fe30.5Ni50.5B19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb8Ni75B17\\n\",\n        \"output\": \" Yes, Nb8Ni75B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Co39W4\\n\",\n        \"output\": \" Yes, Zr7Co39W4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al8(Co5B)7\\n\",\n        \"output\": \" Yes, Al8(Co5B)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.9Mn33Ni0.1\\n\",\n        \"output\": \" Yes, Zr66.9Mn33Ni0.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd4MgNi5\\n\",\n        \"output\": \" Yes, Nd4MgNi5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe80.5P15C4.5\\n\",\n        \"output\": \" Yes, Fe80.5P15C4.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb13V3Si4\\n\",\n        \"output\": \" Yes, Nb13V3Si4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn5Fe91B4\\n\",\n        \"output\": \" No, Mn5Fe91B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe7B2\\n\",\n        \"output\": \" Yes, ZrFe7B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm4Al13Ni3\\n\",\n        \"output\": \" Yes, Sm4Al13Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CrFe39P10\\n\",\n        \"output\": \" Yes, CrFe39P10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.85Cr33Ni0.15\\n\",\n        \"output\": \" Yes, Zr66.85Cr33Ni0.15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr10Ni71P19\\n\",\n        \"output\": \" Yes, Cr10Ni71P19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe40B9C\\n\",\n        \"output\": \" Yes, Fe40B9C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr10Fe13C2\\n\",\n        \"output\": \" No, Cr10Fe13C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn2Al13Si5\\n\",\n        \"output\": \" Yes, Mn2Al13Si5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni17Mo5C3\\n\",\n        \"output\": \" Yes, Ni17Mo5C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al89CoNi10\\n\",\n        \"output\": \" No, Al89CoNi10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf2Ni3\\n\",\n        \"output\": \" Yes, Hf2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11(V2Si)3\\n\",\n        \"output\": \" Yes, Zr11(V2Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdMg5Cu4\\n\",\n        \"output\": \" Yes, NdMg5Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Al9Ni2\\n\",\n        \"output\": \" Yes, La9Al9Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce10Al61Ni29\\n\",\n        \"output\": \" Yes, Ce10Al61Ni29 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ag4.5Pd79\\n\",\n        \"output\": \" Yes, Si16.5Ag4.5Pd79 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr40Fe7Cu53\\n\",\n        \"output\": \" Yes, Zr40Fe7Cu53 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf67(Co10P)3\\n\",\n        \"output\": \" Yes, Hf67(Co10P)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La11Mn4Al5\\n\",\n        \"output\": \" Yes, La11Mn4Al5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y10Mg89Cu\\n\",\n        \"output\": \" No, Y10Mg89Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5.5Fe80B14.5\\n\",\n        \"output\": \" Yes, Zr5.5Fe80B14.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" FeCo7B2\\n\",\n        \"output\": \" Yes, FeCo7B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7V10Co33\\n\",\n        \"output\": \" Yes, Zr7V10Co33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7(Fe27B4)3\\n\",\n        \"output\": \" Yes, Zr7(Fe27B4)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3CuNi6\\n\",\n        \"output\": \" Yes, Zr3CuNi6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg3Ti5Al17\\n\",\n        \"output\": \" Yes, Mg3Ti5Al17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe29B7F14\\n\",\n        \"output\": \" No, Fe29B7F14 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Al4Ni\\n\",\n        \"output\": \" No, Zr5Al4Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni15MoP4\\n\",\n        \"output\": \" Yes, Ni15MoP4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti2.9Al97.1\\n\",\n        \"output\": \" No, Ti2.9Al97.1 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7AlNi2\\n\",\n        \"output\": \" Yes, Zr7AlNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe21B4\\n\",\n        \"output\": \" Yes, Fe21B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Al46Ni\\n\",\n        \"output\": \" No, Nd3Al46Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe53.5Ni18B28.5\\n\",\n        \"output\": \" Yes, Fe53.5Ni18B28.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn25.2Co58.8B16\\n\",\n        \"output\": \" Yes, Mn25.2Co58.8B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co8SiB\\n\",\n        \"output\": \" No, Co8SiB does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Cu7\\n\",\n        \"output\": \" Yes, Ti3Cu7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Al83Ni10\\n\",\n        \"output\": \" Yes, Zr7Al83Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Ni3\\n\",\n        \"output\": \" No, Nd2Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaMg7Ni2\\n\",\n        \"output\": \" Yes, LaMg7Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni42.5P15Pd42.5\\n\",\n        \"output\": \" Yes, Ni42.5P15Pd42.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce5(Al2Cu13)3\\n\",\n        \"output\": \" No, Ce5(Al2Cu13)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe39W2C9\\n\",\n        \"output\": \" No, Fe39W2C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Fe83B10\\n\",\n        \"output\": \" Yes, Ti7Fe83B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti11(AlCu2)3\\n\",\n        \"output\": \" Yes, Ti11(AlCu2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5AlCo44\\n\",\n        \"output\": \" Yes, Zr5AlCo44 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr6.5La66Cu27.5\\n\",\n        \"output\": \" Yes, Sr6.5La66Cu27.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr6.6Fe79B14.4\\n\",\n        \"output\": \" Yes, Cr6.6Fe79B14.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y6Mg15Cu4\\n\",\n        \"output\": \" Yes, Y6Mg15Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti6Nb3Si\\n\",\n        \"output\": \" No, Ti6Nb3Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdAl9\\n\",\n        \"output\": \" Yes, NdAl9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf59Nb26Si15\\n\",\n        \"output\": \" Yes, Hf59Nb26Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg15Ni2\\n\",\n        \"output\": \" Yes, Nd3Mg15Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe63Ni25B12\\n\",\n        \"output\": \" No, Fe63Ni25B12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl8Cr\\n\",\n        \"output\": \" No, CeAl8Cr does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn(Al29Ni4)3\\n\",\n        \"output\": \" Yes, Mn(Al29Ni4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr15Fe73B12\\n\",\n        \"output\": \" Yes, Cr15Fe73B12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9Al9Ni7\\n\",\n        \"output\": \" Yes, Zr9Al9Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti15VSi4\\n\",\n        \"output\": \" Yes, Ti15VSi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co31B19\\n\",\n        \"output\": \" Yes, Co31B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ba2(La9Cu7)3\\n\",\n        \"output\": \" Yes, Ba2(La9Cu7)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd21Fe79\\n\",\n        \"output\": \" Yes, Nd21Fe79 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce25.5Al62.5Fe12\\n\",\n        \"output\": \" No, Ce25.5Al62.5Fe12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al5Cu43\\n\",\n        \"output\": \" No, Ce2Al5Cu43 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe85(B4C)3\\n\",\n        \"output\": \" Yes, Fe85(B4C)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y(Mg2Ag)3\\n\",\n        \"output\": \" Yes, Y(Mg2Ag)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" rule\\n\",\n        \"output\": \" rule is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al6(Co3B)11\\n\",\n        \"output\": \" Yes, Al6(Co3B)11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni10P19Pd71\\n\",\n        \"output\": \" Yes, Ni10P19Pd71 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb3Fe2Co15\\n\",\n        \"output\": \" Yes, Nb3Fe2Co15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al8(Ni5B)7\\n\",\n        \"output\": \" No, Al8(Ni5B)7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti23(Al9Ni2)7\\n\",\n        \"output\": \" Yes, Ti23(Al9Ni2)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La11Al5Zn4\\n\",\n        \"output\": \" Yes, La11Al5Zn4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Fe23\\n\",\n        \"output\": \" Yes, Zr2Fe23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni15BC4\\n\",\n        \"output\": \" No, Ni15BC4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ta5(NbNi4)3\\n\",\n        \"output\": \" Yes, Ta5(NbNi4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2Cr5Fe13\\n\",\n        \"output\": \" Yes, Zr2Cr5Fe13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr12Cr3Ni5\\n\",\n        \"output\": \" Yes, Zr12Cr3Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Mg10Cu7\\n\",\n        \"output\": \" Yes, Nd3Mg10Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf9.8Fe87.9B2.3\\n\",\n        \"output\": \" Yes, Hf9.8Fe87.9B2.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe33W7C10\\n\",\n        \"output\": \" Yes, Fe33W7C10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr5La58Cu37\\n\",\n        \"output\": \" Yes, Sr5La58Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co7Ni73.5P19.5\\n\",\n        \"output\": \" Yes, Co7Ni73.5P19.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu67Ni17P16\\n\",\n        \"output\": \" Yes, Cu67Ni17P16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr55.93Ni28.93P15.14\\n\",\n        \"output\": \" Yes, Cr55.93Ni28.93P15.14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn6Nb15Co79\\n\",\n        \"output\": \" Yes, Mn6Nb15Co79 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al91FeNi8\\n\",\n        \"output\": \" No, Al91FeNi8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr8Co12C5\\n\",\n        \"output\": \" Yes, Cr8Co12C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu4.2Si16.5Pd79.3\\n\",\n        \"output\": \" Yes, Cu4.2Si16.5Pd79.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg8Cu\\n\",\n        \"output\": \" Yes, NdMg8Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7Al2Ni\\n\",\n        \"output\": \" Yes, La7Al2Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al46CoNi3\\n\",\n        \"output\": \" No, Al46CoNi3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe85CuB14\\n\",\n        \"output\": \" No, Fe85CuB14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Si4Ni7\\n\",\n        \"output\": \" Yes, Ti9Si4Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni81.5B1.8P16.7\\n\",\n        \"output\": \" Yes, Ni81.5B1.8P16.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16Ni76.5B7.5\\n\",\n        \"output\": \" No, Si16Ni76.5B7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Al4Cu3\\n\",\n        \"output\": \" No, La3Al4Cu3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr27Cu23\\n\",\n        \"output\": \" No, Zr27Cu23 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La5Al13Ni2\\n\",\n        \"output\": \" No, La5Al13Ni2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe84B7P9\\n\",\n        \"output\": \" No, Fe84B7P9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni16Mo5C4\\n\",\n        \"output\": \" Yes, Ni16Mo5C4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al87Fe2Ni11\\n\",\n        \"output\": \" Yes, Al87Fe2Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83B12P5\\n\",\n        \"output\": \" Yes, Fe83B12P5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2Cu53Ag45\\n\",\n        \"output\": \" No, Ce2Cu53Ag45 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni26B17C7\\n\",\n        \"output\": \" Yes, Ni26B17C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni78.5B11.5C10\\n\",\n        \"output\": \" No, Ni78.5B11.5C10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni17(B3C)2\\n\",\n        \"output\": \" Yes, Ni17(B3C)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Dy0.3Zr10Fe89.7\\n\",\n        \"output\": \" Yes, Dy0.3Zr10Fe89.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al45Fe2Co3\\n\",\n        \"output\": \" No, Al45Fe2Co3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe91(CuB2)3\\n\",\n        \"output\": \" No, Fe91(CuB2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al13V3Cu4\\n\",\n        \"output\": \" Yes, Al13V3Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al17Cr3\\n\",\n        \"output\": \" No, Al17Cr3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf28.8Nb33Cu38.2\\n\",\n        \"output\": \" Yes, Hf28.8Nb33Cu38.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Al17\\n\",\n        \"output\": \" Yes, Y3Al17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Yb11Cu39\\n\",\n        \"output\": \" Yes, Yb11Cu39 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf58(V9Si5)3\\n\",\n        \"output\": \" Yes, Hf58(V9Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Cu2\\n\",\n        \"output\": \" No, La3Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13V10Ni27\\n\",\n        \"output\": \" Yes, Zr13V10Ni27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr67Fe20.2Ni12.8\\n\",\n        \"output\": \" Yes, Zr67Fe20.2Ni12.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al10Co31B9\\n\",\n        \"output\": \" No, Al10Co31B9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl47Cr2\\n\",\n        \"output\": \" No, CeAl47Cr2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2Ni3\\n\",\n        \"output\": \" No, La2Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrCo8W\\n\",\n        \"output\": \" Yes, ZrCo8W has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3Cu2Ni5\\n\",\n        \"output\": \" No, Ti3Cu2Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAl23Ni\\n\",\n        \"output\": \" No, MnAl23Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si2.5Ni75.5B22\\n\",\n        \"output\": \" No, Si2.5Ni75.5B22 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd0.3Zr10Fe89.7\\n\",\n        \"output\": \" Yes, Gd0.3Zr10Fe89.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf6CuNi3\\n\",\n        \"output\": \" Yes, Hf6CuNi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr62.5Be32.5Nb5\\n\",\n        \"output\": \" Yes, Zr62.5Be32.5Nb5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr17AlNi2\\n\",\n        \"output\": \" Yes, Zr17AlNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf7Cu3\\n\",\n        \"output\": \" Yes, Hf7Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu10Si16.5Pd73.5\\n\",\n        \"output\": \" Yes, Cu10Si16.5Pd73.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe79(B5P2)3\\n\",\n        \"output\": \" Yes, Fe79(B5P2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La83Al5Ni12\\n\",\n        \"output\": \" Yes, La83Al5Ni12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8Fe85B7\\n\",\n        \"output\": \" Yes, Zr8Fe85B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81CuB18\\n\",\n        \"output\": \" No, Fe81CuB18 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5.2Co84.8Mo10\\n\",\n        \"output\": \" Yes, Zr5.2Co84.8Mo10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" spaghetti\\n\",\n        \"output\": \" spaghetti is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb80Si19C\\n\",\n        \"output\": \" Yes, Nb80Si19C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B16P3\\n\",\n        \"output\": \" Yes, Fe81B16P3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La12Al3Cu5\\n\",\n        \"output\": \" Yes, La12Al3Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf61(V8Si5)3\\n\",\n        \"output\": \" Yes, Hf61(V8Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr60.8Al5Ni34.2\\n\",\n        \"output\": \" Yes, Zr60.8Al5Ni34.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7(AlNi2)6\\n\",\n        \"output\": \" Yes, Zr7(AlNi2)6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca14(MgAl)3\\n\",\n        \"output\": \" Yes, Ca14(MgAl)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn1Al86.5Ni12.5\\n\",\n        \"output\": \" Yes, Mn1Al86.5Ni12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn39Co49B12\\n\",\n        \"output\": \" Yes, Mn39Co49B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7Ni3\\n\",\n        \"output\": \" Yes, Ti7Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al71Cr4Si25\\n\",\n        \"output\": \" Yes, Al71Cr4Si25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaMg3Cu\\n\",\n        \"output\": \" No, LaMg3Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba4La31Cu15\\n\",\n        \"output\": \" Yes, Ba4La31Cu15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Al5Ni8\\n\",\n        \"output\": \" Yes, Zr7Al5Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sm3Al14Ni3\\n\",\n        \"output\": \" Yes, Sm3Al14Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdMg15Cu4\\n\",\n        \"output\": \" Yes, NdMg15Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe72(SiB3)7\\n\",\n        \"output\": \" Yes, Fe72(SiB3)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr33Nb10Cu57\\n\",\n        \"output\": \" Yes, Zr33Nb10Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.85Co33Ni0.15\\n\",\n        \"output\": \" Yes, Zr66.85Co33Ni0.15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe23Ni60B17\\n\",\n        \"output\": \" Yes, Fe23Ni60B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe42Ni5B3\\n\",\n        \"output\": \" No, Fe42Ni5B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10.5Co79.5Mo10\\n\",\n        \"output\": \" Yes, Zr10.5Co79.5Mo10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co16B4C5\\n\",\n        \"output\": \" No, Co16B4C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7Al8Ni5\\n\",\n        \"output\": \" Yes, La7Al8Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Mg3Ni5\\n\",\n        \"output\": \" No, Nd2Mg3Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg14Cu5\\n\",\n        \"output\": \" Yes, CeMg14Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg11Cu6\\n\",\n        \"output\": \" Yes, Nd3Mg11Cu6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni9P2Pd9\\n\",\n        \"output\": \" Yes, Ni9P2Pd9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Al3Ni7\\n\",\n        \"output\": \" Yes, Zr10Al3Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al45Fe3Ni2\\n\",\n        \"output\": \" No, Al45Fe3Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr22(Ni7Mo19)3\\n\",\n        \"output\": \" Yes, Cr22(Ni7Mo19)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnAl47Ni2\\n\",\n        \"output\": \" No, MnAl47Ni2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al8(Ni9B5)3\\n\",\n        \"output\": \" Yes, Al8(Ni9B5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Cu3Ni5\\n\",\n        \"output\": \" Yes, Zr12Cu3Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al6Co35B9\\n\",\n        \"output\": \" Yes, Al6Co35B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti42Al23Ni35\\n\",\n        \"output\": \" Yes, Ti42Al23Ni35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9Be\\n\",\n        \"output\": \" No, Zr9Be does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaMg8Cu\\n\",\n        \"output\": \" No, LaMg8Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf9.5Fe48.9O41.6\\n\",\n        \"output\": \" No, Hf9.5Fe48.9O41.6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni17B7C\\n\",\n        \"output\": \" Yes, Ni17B7C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe80B11C9\\n\",\n        \"output\": \" Yes, Fe80B11C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La13Al71Ni16\\n\",\n        \"output\": \" Yes, La13Al71Ni16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr35Fe14Ru\\n\",\n        \"output\": \" Yes, Zr35Fe14Ru has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg15Ni4\\n\",\n        \"output\": \" Yes, YMg15Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" AlCu\\n\",\n        \"output\": \" No, AlCu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Al23\\n\",\n        \"output\": \" Yes, Ce2Al23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd27.7Fe56.3B16\\n\",\n        \"output\": \" Yes, Nd27.7Fe56.3B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La11Al5Cr4\\n\",\n        \"output\": \" Yes, La11Al5Cr4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co16B7C2\\n\",\n        \"output\": \" Yes, Co16B7C2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La12Al5Cu3\\n\",\n        \"output\": \" Yes, La12Al5Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr14(SiMo)3\\n\",\n        \"output\": \" Yes, Zr14(SiMo)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr48Al25Ni27\\n\",\n        \"output\": \" Yes, Zr48Al25Ni27 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrTiSi3\\n\",\n        \"output\": \" Yes, ZrTiSi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrTi9\\n\",\n        \"output\": \" No, ZrTi9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Cu2Ni\\n\",\n        \"output\": \" Yes, Ti2Cu2Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeMg17Cu2\\n\",\n        \"output\": \" Yes, CeMg17Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce5(AlCu14)3\\n\",\n        \"output\": \" Yes, Ce5(AlCu14)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y4(MgCu)3\\n\",\n        \"output\": \" No, Y4(MgCu)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co7B3\\n\",\n        \"output\": \" Yes, Co7B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Al6Ni5\\n\",\n        \"output\": \" Yes, La9Al6Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al12Co21B17\\n\",\n        \"output\": \" Yes, Al12Co21B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al2(Co13B3)3\\n\",\n        \"output\": \" Yes, Al2(Co13B3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Al44Ni3\\n\",\n        \"output\": \" Yes, La3Al44Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn30.4Co45.6B24\\n\",\n        \"output\": \" Yes, Mn30.4Co45.6B24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2.5Mg93.5Mn4\\n\",\n        \"output\": \" No, Y2.5Mg93.5Mn4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr3Fe37P10\\n\",\n        \"output\": \" Yes, Cr3Fe37P10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe6Cu19\\n\",\n        \"output\": \" No, Fe6Cu19 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe33Ag67\\n\",\n        \"output\": \" No, Fe33Ag67 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr38.7Nb10Cu51.3\\n\",\n        \"output\": \" Yes, Zr38.7Nb10Cu51.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Pd80.5Au3\\n\",\n        \"output\": \" Yes, Si16.5Pd80.5Au3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Fe37B11\\n\",\n        \"output\": \" Yes, Al2Fe37B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co12Mo8C5\\n\",\n        \"output\": \" Yes, Co12Mo8C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Al87Ni10\\n\",\n        \"output\": \" Yes, Zr3Al87Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al3Cu2\\n\",\n        \"output\": \" No, Al3Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La12Al5Ni3\\n\",\n        \"output\": \" Yes, La12Al5Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La4Cu\\n\",\n        \"output\": \" No, La4Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg7Al4Ag9\\n\",\n        \"output\": \" Yes, Mg7Al4Ag9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni33B7C10\\n\",\n        \"output\": \" No, Ni33B7C10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si2Ni7C\\n\",\n        \"output\": \" No, Si2Ni7C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Co17B6\\n\",\n        \"output\": \" Yes, Mn2Co17B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7Fe92B\\n\",\n        \"output\": \" Yes, Zr7Fe92B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La13Al3Ni4\\n\",\n        \"output\": \" Yes, La13Al3Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti9AlCu10\\n\",\n        \"output\": \" Yes, Ti9AlCu10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe41Ni5B4\\n\",\n        \"output\": \" No, Fe41Ni5B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe39W4C7\\n\",\n        \"output\": \" No, Fe39W4C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr63.5Be32.5Nb4\\n\",\n        \"output\": \" Yes, Zr63.5Be32.5Nb4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Al13Ni4\\n\",\n        \"output\": \" Yes, Ce3Al13Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf42NbCu57\\n\",\n        \"output\": \" Yes, Hf42NbCu57 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SiB5Mo14\\n\",\n        \"output\": \" No, SiB5Mo14 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr3Si10Pd37\\n\",\n        \"output\": \" Yes, Cr3Si10Pd37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al10Co27B13\\n\",\n        \"output\": \" Yes, Al10Co27B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr42.5Cu55B2.5\\n\",\n        \"output\": \" Yes, Zr42.5Cu55B2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al7Ni3\\n\",\n        \"output\": \" No, Al7Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf52(V11Si5)3\\n\",\n        \"output\": \" Yes, Hf52(V11Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ikebana\\n\",\n        \"output\": \" ikebana is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr85(Si4C)3\\n\",\n        \"output\": \" No, Zr85(Si4C)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr14(AlNi)3\\n\",\n        \"output\": \" Yes, Zr14(AlNi)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni34B11C5\\n\",\n        \"output\": \" Yes, Ni34B11C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11Nb8Si\\n\",\n        \"output\": \" No, Zr11Nb8Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" MnGe9Pd40\\n\",\n        \"output\": \" Yes, MnGe9Pd40 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg23(Ti2Al5)11\\n\",\n        \"output\": \" No, Mg23(Ti2Al5)11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.8Cu33Ni0.2\\n\",\n        \"output\": \" Yes, Zr66.8Cu33Ni0.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co5Ni77P18\\n\",\n        \"output\": \" Yes, Co5Ni77P18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni2PPt2\\n\",\n        \"output\": \" Yes, Ni2PPt2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce10Nb13Al77\\n\",\n        \"output\": \" No, Ce10Nb13Al77 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce18Al77Fe5\\n\",\n        \"output\": \" No, Ce18Al77Fe5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4(Al2Ni)7\\n\",\n        \"output\": \" Yes, La4(Al2Ni)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si(Ni7B)3\\n\",\n        \"output\": \" No, Si(Ni7B)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni20P19Pd61\\n\",\n        \"output\": \" Yes, Ni20P19Pd61 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" HfTa4Fe5\\n\",\n        \"output\": \" Yes, HfTa4Fe5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn7Co13B5\\n\",\n        \"output\": \" Yes, Mn7Co13B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr60.3Ti10Ni29.7\\n\",\n        \"output\": \" Yes, Zr60.3Ti10Ni29.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2Mg3Cu5\\n\",\n        \"output\": \" Yes, Nd2Mg3Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg3Ti27Al70\\n\",\n        \"output\": \" No, Mg3Ti27Al70 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si5B2Mo13\\n\",\n        \"output\": \" No, Si5B2Mo13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al67(Fe7Ni4)3\\n\",\n        \"output\": \" No, Al67(Fe7Ni4)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe73W10C17\\n\",\n        \"output\": \" No, Fe73W10C17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" north\\n\",\n        \"output\": \" north is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg5Al2Zn3\\n\",\n        \"output\": \" No, Mg5Al2Zn3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2MgAg2\\n\",\n        \"output\": \" No, Y2MgAg2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti17CuNi2\\n\",\n        \"output\": \" No, Ti17CuNi2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" industry\\n\",\n        \"output\": \" industry is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co17(SiB)4\\n\",\n        \"output\": \" Yes, Co17(SiB)4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce6Cu79Ag15\\n\",\n        \"output\": \" Yes, Ce6Cu79Ag15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La22Al61Ni17\\n\",\n        \"output\": \" Yes, La22Al61Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe13Si20Pd67\\n\",\n        \"output\": \" Yes, Fe13Si20Pd67 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Pd71Au12.5\\n\",\n        \"output\": \" Yes, Si16.5Pd71Au12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y5Mg93Mn2\\n\",\n        \"output\": \" No, Y5Mg93Mn2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca2MgAl17\\n\",\n        \"output\": \" Yes, Ca2MgAl17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr35Fe14Ir\\n\",\n        \"output\": \" Yes, Zr35Fe14Ir has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10V0.054Fe89.946\\n\",\n        \"output\": \" Yes, Zr10V0.054Fe89.946 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al15V2Ge3\\n\",\n        \"output\": \" No, Al15V2Ge3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn(Al2Si)3\\n\",\n        \"output\": \" Yes, Mn(Al2Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" AlFe17Si2\\n\",\n        \"output\": \" Yes, AlFe17Si2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7Fe78.7B14.3\\n\",\n        \"output\": \" Yes, Nb7Fe78.7B14.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al69Fe6Ge25\\n\",\n        \"output\": \" Yes, Al69Fe6Ge25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg3Ag4\\n\",\n        \"output\": \" Yes, Y3Mg3Ag4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe81B10C9\\n\",\n        \"output\": \" Yes, Fe81B10C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al34(Si7Mo15)3\\n\",\n        \"output\": \" Yes, Al34(Si7Mo15)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ba9.5La52.5Cu38\\n\",\n        \"output\": \" Yes, Ba9.5La52.5Cu38 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta3NbNi6\\n\",\n        \"output\": \" Yes, Ta3NbNi6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ScFe9\\n\",\n        \"output\": \" Yes, ScFe9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe5Co3B2\\n\",\n        \"output\": \" Yes, Fe5Co3B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg9Al4Ag7\\n\",\n        \"output\": \" Yes, Mg9Al4Ag7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr9Fe76B15\\n\",\n        \"output\": \" Yes, Cr9Fe76B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4Ni\\n\",\n        \"output\": \" Yes, Zr4Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe81Ni15B4\\n\",\n        \"output\": \" No, Fe81Ni15B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr6Fe16B3\\n\",\n        \"output\": \" Yes, Cr6Fe16B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Al13Ni4\\n\",\n        \"output\": \" Yes, La3Al13Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf38Nb5Cu57\\n\",\n        \"output\": \" Yes, Hf38Nb5Cu57 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr60.3Mn10Ni29.7\\n\",\n        \"output\": \" Yes, Zr60.3Mn10Ni29.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co2(Ni11P3)7\\n\",\n        \"output\": \" Yes, Co2(Ni11P3)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg15Ti49Al36\\n\",\n        \"output\": \" No, Mg15Ti49Al36 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al13Cr5Si2\\n\",\n        \"output\": \" No, Al13Cr5Si2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti8CuNi\\n\",\n        \"output\": \" No, Ti8CuNi does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Al44Ni3\\n\",\n        \"output\": \" Yes, Nd3Al44Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe95CuB4\\n\",\n        \"output\": \" No, Fe95CuB4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr24Cu75B\\n\",\n        \"output\": \" No, Zr24Cu75B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5(Al2Cu13)3\\n\",\n        \"output\": \" No, Nd5(Al2Cu13)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe72.5Si5B22.5\\n\",\n        \"output\": \" Yes, Fe72.5Si5B22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al62.5Fe12.5Cu25\\n\",\n        \"output\": \" No, Al62.5Fe12.5Cu25 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Mg85Zn12\\n\",\n        \"output\": \" Yes, Ce3Mg85Zn12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Co17B5\\n\",\n        \"output\": \" Yes, Ti3Co17B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2CuNi\\n\",\n        \"output\": \" Yes, Zr2CuNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr12.5La50.5Cu37\\n\",\n        \"output\": \" Yes, Sr12.5La50.5Cu37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" kamikaze\\n\",\n        \"output\": \" kamikaze is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ta8(Ti3Si)3\\n\",\n        \"output\": \" Yes, Ta8(Ti3Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti11Be8Si\\n\",\n        \"output\": \" No, Ti11Be8Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr9La54Cu37\\n\",\n        \"output\": \" Yes, Sr9La54Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe33W8C9\\n\",\n        \"output\": \" No, Fe33W8C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti16VSi3\\n\",\n        \"output\": \" Yes, Ti16VSi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe67Ni25B8\\n\",\n        \"output\": \" No, Fe67Ni25B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe42B3P5\\n\",\n        \"output\": \" No, Fe42B3P5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce5Al88Cu7\\n\",\n        \"output\": \" No, Ce5Al88Cu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Al2\\n\",\n        \"output\": \" Yes, La3Al2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeMg3Cu\\n\",\n        \"output\": \" No, CeMg3Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al21Co5Ge24\\n\",\n        \"output\": \" Yes, Al21Co5Ge24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnFe89B10\\n\",\n        \"output\": \" No, MnFe89B10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu73Ni11P16\\n\",\n        \"output\": \" Yes, Cu73Ni11P16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg16Ag3\\n\",\n        \"output\": \" Yes, YMg16Ag3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb3Fe16B\\n\",\n        \"output\": \" No, Nb3Fe16B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La43Al4Ni3\\n\",\n        \"output\": \" Yes, La43Al4Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg4Cu\\n\",\n        \"output\": \" Yes, Mg4Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co29B20C\\n\",\n        \"output\": \" No, Co29B20C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd5Mg7Ni8\\n\",\n        \"output\": \" Yes, Nd5Mg7Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAl2Ni\\n\",\n        \"output\": \" Yes, LaAl2Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y5Mg41Mn4\\n\",\n        \"output\": \" No, Y5Mg41Mn4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr33Al35Ni32\\n\",\n        \"output\": \" Yes, Zr33Al35Ni32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7Cu2Ni\\n\",\n        \"output\": \" Yes, Zr7Cu2Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Ag12.5Pd71\\n\",\n        \"output\": \" Yes, Si16.5Ag12.5Pd71 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta7Fe83B10\\n\",\n        \"output\": \" Yes, Ta7Fe83B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr16TiSi3\\n\",\n        \"output\": \" Yes, Zr16TiSi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce5Mn2Al43\\n\",\n        \"output\": \" Yes, Ce5Mn2Al43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79(B2W)7\\n\",\n        \"output\": \" Yes, Fe79(B2W)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CaAl9\\n\",\n        \"output\": \" Yes, CaAl9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La7Al2Ni11\\n\",\n        \"output\": \" Yes, La7Al2Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co36(WC)7\\n\",\n        \"output\": \" Yes, Co36(WC)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce5Al87Ni8\\n\",\n        \"output\": \" Yes, Ce5Al87Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Mg14Cu3\\n\",\n        \"output\": \" Yes, Ce3Mg14Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" V15Fe69B16\\n\",\n        \"output\": \" Yes, V15Fe69B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe7Si2C\\n\",\n        \"output\": \" Yes, Fe7Si2C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr16.5Cr16Co67.5\\n\",\n        \"output\": \" Yes, Zr16.5Cr16Co67.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al33Si12Ni5\\n\",\n        \"output\": \" Yes, Al33Si12Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe15Si3B2\\n\",\n        \"output\": \" Yes, Fe15Si3B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr13(Al19Ni10)3\\n\",\n        \"output\": \" Yes, Zr13(Al19Ni10)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn67Co17B16\\n\",\n        \"output\": \" Yes, Mn67Co17B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti27Cu73\\n\",\n        \"output\": \" Yes, Ti27Cu73 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2Mg3Ag5\\n\",\n        \"output\": \" Yes, Y2Mg3Ag5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3Ni14C3\\n\",\n        \"output\": \" No, Si3Ni14C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg13(Ti2Al)29\\n\",\n        \"output\": \" Yes, Mg13(Ti2Al)29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Fe78B17\\n\",\n        \"output\": \" Yes, Zr5Fe78B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr19Co20C11\\n\",\n        \"output\": \" Yes, Cr19Co20C11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Al3Cu4\\n\",\n        \"output\": \" Yes, Zr13Al3Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu13(Ni23P6)3\\n\",\n        \"output\": \" No, Cu13(Ni23P6)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" GdAl15Ni4\\n\",\n        \"output\": \" No, GdAl15Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta13Ni70B17\\n\",\n        \"output\": \" Yes, Ta13Ni70B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" FeB5W14\\n\",\n        \"output\": \" Yes, FeB5W14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti13Si4Ni3\\n\",\n        \"output\": \" No, Ti13Si4Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al14(FeNi)3\\n\",\n        \"output\": \" Yes, Al14(FeNi)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe15P3C2\\n\",\n        \"output\": \" Yes, Fe15P3C2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr15Co24C11\\n\",\n        \"output\": \" No, Cr15Co24C11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" GdZr5Fe44\\n\",\n        \"output\": \" Yes, GdZr5Fe44 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaMg16Ni3\\n\",\n        \"output\": \" Yes, LaMg16Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5(Fe4Ni)9\\n\",\n        \"output\": \" Yes, Zr5(Fe4Ni)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" B3Mo17\\n\",\n        \"output\": \" No, B3Mo17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y4Al13Ni3\\n\",\n        \"output\": \" No, Y4Al13Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Mg15Ni\\n\",\n        \"output\": \" Yes, Nd4Mg15Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg18AlZn\\n\",\n        \"output\": \" No, Mg18AlZn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl23Ni\\n\",\n        \"output\": \" No, NdAl23Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Co3\\n\",\n        \"output\": \" Yes, Zr7Co3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sm11Al5Ni4\\n\",\n        \"output\": \" Yes, Sm11Al5Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al18FeCu\\n\",\n        \"output\": \" Yes, Al18FeCu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3CuNi\\n\",\n        \"output\": \" Yes, Zr3CuNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti2AlNi2\\n\",\n        \"output\": \" Yes, Ti2AlNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YAl3Ni\\n\",\n        \"output\": \" Yes, YAl3Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf8(Nb3Si)3\\n\",\n        \"output\": \" Yes, Hf8(Nb3Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr59Cu40B\\n\",\n        \"output\": \" Yes, Zr59Cu40B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7CuNi2\\n\",\n        \"output\": \" Yes, Zr7CuNi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr15Fe77B8\\n\",\n        \"output\": \" No, Cr15Fe77B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf59V26Si15\\n\",\n        \"output\": \" Yes, Hf59V26Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Al25Ni16\\n\",\n        \"output\": \" Yes, La9Al25Ni16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti6AlCu3\\n\",\n        \"output\": \" Yes, Ti6AlCu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeNbAl18\\n\",\n        \"output\": \" No, CeNbAl18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg5Ti29Al66\\n\",\n        \"output\": \" Yes, Mg5Ti29Al66 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdMgCu3\\n\",\n        \"output\": \" Yes, NdMgCu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf17Si3\\n\",\n        \"output\": \" Yes, Hf17Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn35.2Co52.8B12\\n\",\n        \"output\": \" Yes, Mn35.2Co52.8B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al67V13Cu20\\n\",\n        \"output\": \" Yes, Al67V13Cu20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8CuNi\\n\",\n        \"output\": \" No, Zr8CuNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" woolen\\n\",\n        \"output\": \" woolen is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe85P12.5C2.5\\n\",\n        \"output\": \" No, Fe85P12.5C2.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe59B10F31\\n\",\n        \"output\": \" No, Fe59B10F31 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni81.5B18.5\\n\",\n        \"output\": \" Yes, Ni81.5B18.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15.4Co68.6Mo16\\n\",\n        \"output\": \" Yes, Zr15.4Co68.6Mo16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" point\\n\",\n        \"output\": \" point is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al46FeCo3\\n\",\n        \"output\": \" No, Al46FeCo3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al16V3Cu\\n\",\n        \"output\": \" No, Al16V3Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg4AlZn5\\n\",\n        \"output\": \" No, Mg4AlZn5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr42NbCu57\\n\",\n        \"output\": \" Yes, Zr42NbCu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si15Pd81Au4\\n\",\n        \"output\": \" Yes, Si15Pd81Au4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La13Al79Ni8\\n\",\n        \"output\": \" Yes, La13Al79Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg17Al52Pd31\\n\",\n        \"output\": \" No, Mg17Al52Pd31 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CaMg17Zn2\\n\",\n        \"output\": \" No, CaMg17Zn2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr57Fe18B25\\n\",\n        \"output\": \" Yes, Zr57Fe18B25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81.5Si12.5B6\\n\",\n        \"output\": \" No, Fe81.5Si12.5B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SrLa62Cu37\\n\",\n        \"output\": \" Yes, SrLa62Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80B7P13\\n\",\n        \"output\": \" Yes, Fe80B7P13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti2Al2Cu\\n\",\n        \"output\": \" No, Ti2Al2Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca7.5Al87.5Ni5\\n\",\n        \"output\": \" Yes, Ca7.5Al87.5Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Cu7Ni\\n\",\n        \"output\": \" No, Zr2Cu7Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf8(Zr3Si)3\\n\",\n        \"output\": \" Yes, Hf8(Zr3Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe56Ni19B25\\n\",\n        \"output\": \" Yes, Fe56Ni19B25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr8Co41W\\n\",\n        \"output\": \" Yes, Zr8Co41W has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Mg16Ni\\n\",\n        \"output\": \" No, La3Mg16Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe7Ni2B\\n\",\n        \"output\": \" No, Fe7Ni2B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Pd79.3Au4.2\\n\",\n        \"output\": \" Yes, Si16.5Pd79.3Au4.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeCu5Ag4\\n\",\n        \"output\": \" Yes, CeCu5Ag4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn23Co57B20\\n\",\n        \"output\": \" Yes, Mn23Co57B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe18Ni5B2\\n\",\n        \"output\": \" No, Fe18Ni5B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca7MgCu2\\n\",\n        \"output\": \" Yes, Ca7MgCu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn3Al45Co2\\n\",\n        \"output\": \" No, Mn3Al45Co2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" jumbo\\n\",\n        \"output\": \" jumbo is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl8Ni\\n\",\n        \"output\": \" Yes, CeAl8Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr61Fe19B20\\n\",\n        \"output\": \" Yes, Zr61Fe19B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti4Al5Cu11\\n\",\n        \"output\": \" Yes, Ti4Al5Cu11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf38.7Nb10Cu51.3\\n\",\n        \"output\": \" Yes, Hf38.7Nb10Cu51.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al4Co33B13\\n\",\n        \"output\": \" Yes, Al4Co33B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn5Fe38B7\\n\",\n        \"output\": \" Yes, Mn5Fe38B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca9Al91\\n\",\n        \"output\": \" Yes, Ca9Al91 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaMg4Cu5\\n\",\n        \"output\": \" Yes, LaMg4Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni41B8C\\n\",\n        \"output\": \" Yes, Ni41B8C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb40Si9Ge\\n\",\n        \"output\": \" Yes, Nb40Si9Ge has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni72Mo9P19\\n\",\n        \"output\": \" Yes, Ni72Mo9P19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti9Al3Cu8\\n\",\n        \"output\": \" Yes, Ti9Al3Cu8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si5Ni13C2\\n\",\n        \"output\": \" No, Si5Ni13C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y15Mg81Mn4\\n\",\n        \"output\": \" No, Y15Mg81Mn4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn21Co47B32\\n\",\n        \"output\": \" Yes, Mn21Co47B32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn31Co41B28\\n\",\n        \"output\": \" Yes, Mn31Co41B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn9Co11B5\\n\",\n        \"output\": \" Yes, Mn9Co11B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn7.2Co64.8B28\\n\",\n        \"output\": \" Yes, Mn7.2Co64.8B28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce6Al89V5\\n\",\n        \"output\": \" No, Ce6Al89V5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni52.5P25Pt22.5\\n\",\n        \"output\": \" Yes, Ni52.5P25Pt22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.9V0.1Ni33\\n\",\n        \"output\": \" Yes, Zr66.9V0.1Ni33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn74Si23P3\\n\",\n        \"output\": \" Yes, Mn74Si23P3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe91NiB8\\n\",\n        \"output\": \" No, Fe91NiB8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg4\\n\",\n        \"output\": \" No, YMg4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni18Mo5C2\\n\",\n        \"output\": \" No, Ni18Mo5C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Fe2\\n\",\n        \"output\": \" Yes, Nd3Fe2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf64(Nb7Si5)3\\n\",\n        \"output\": \" Yes, Hf64(Nb7Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La43Al5Ni2\\n\",\n        \"output\": \" Yes, La43Al5Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4Al11Ni5\\n\",\n        \"output\": \" Yes, La4Al11Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrCu\\n\",\n        \"output\": \" Yes, ZrCu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni81P19\\n\",\n        \"output\": \" Yes, Ni81P19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si22.5B7.5Mo70\\n\",\n        \"output\": \" Yes, Si22.5B7.5Mo70 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr34Fe11Si5\\n\",\n        \"output\": \" Yes, Zr34Fe11Si5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y12Mg5Cu8\\n\",\n        \"output\": \" Yes, Y12Mg5Cu8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La27Al9Ni64\\n\",\n        \"output\": \" Yes, La27Al9Ni64 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAl4Ni5\\n\",\n        \"output\": \" No, LaAl4Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37W6C7\\n\",\n        \"output\": \" No, Fe37W6C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb5Si2Mo3\\n\",\n        \"output\": \" Yes, Nb5Si2Mo3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni75B17C8\\n\",\n        \"output\": \" No, Ni75B17C8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr33Ni67\\n\",\n        \"output\": \" Yes, Zr33Ni67 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl8Cu\\n\",\n        \"output\": \" No, LaAl8Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn7Co65B28\\n\",\n        \"output\": \" Yes, Mn7Co65B28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Fe89.964Si0.036\\n\",\n        \"output\": \" Yes, Zr10Fe89.964Si0.036 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37Mo4C9\\n\",\n        \"output\": \" Yes, Fe37Mo4C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La7Al4Ni9\\n\",\n        \"output\": \" Yes, La7Al4Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" hook\\n\",\n        \"output\": \" hook is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd4(MgNi)3\\n\",\n        \"output\": \" Yes, Nd4(MgNi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2(Mg5Ni)3\\n\",\n        \"output\": \" Yes, Ce2(Mg5Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al89Fe5Ni6\\n\",\n        \"output\": \" No, Al89Fe5Ni6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni30B11C9\\n\",\n        \"output\": \" Yes, Ni30B11C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" cylinder\\n\",\n        \"output\": \" cylinder is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al5V2Ge3\\n\",\n        \"output\": \" No, Al5V2Ge3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrTi3Si16\\n\",\n        \"output\": \" Yes, ZrTi3Si16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al8(Fe11B3)3\\n\",\n        \"output\": \" Yes, Al8(Fe11B3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr13Co28C9\\n\",\n        \"output\": \" Yes, Cr13Co28C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe72.5P20C7.5\\n\",\n        \"output\": \" Yes, Fe72.5P20C7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeNb2Al17\\n\",\n        \"output\": \" No, CeNb2Al17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe52.5B24.5N23\\n\",\n        \"output\": \" Yes, Fe52.5B24.5N23 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd67.5B10Au22.5\\n\",\n        \"output\": \" Yes, Gd67.5B10Au22.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7.5Al85Mo7.5\\n\",\n        \"output\": \" Yes, La7.5Al85Mo7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al21Fe5Ge24\\n\",\n        \"output\": \" Yes, Al21Fe5Ge24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si7Ni36B7\\n\",\n        \"output\": \" Yes, Si7Ni36B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Al0.036Fe89.964\\n\",\n        \"output\": \" Yes, Zr10Al0.036Fe89.964 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Tb28.3Fe56.7Si15\\n\",\n        \"output\": \" Yes, Tb28.3Fe56.7Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr59Nb30Si11\\n\",\n        \"output\": \" No, Zr59Nb30Si11 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7.8Fe78.4B13.8\\n\",\n        \"output\": \" Yes, Nb7.8Fe78.4B13.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni27B20C3\\n\",\n        \"output\": \" No, Ni27B20C3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti11Si4Ni5\\n\",\n        \"output\": \" No, Ti11Si4Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr12Ti5Si3\\n\",\n        \"output\": \" Yes, Zr12Ti5Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al42Fe7Si\\n\",\n        \"output\": \" No, Al42Fe7Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Fe84.5B8.5\\n\",\n        \"output\": \" Yes, Zr7Fe84.5B8.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb15VSi4\\n\",\n        \"output\": \" Yes, Nb15VSi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7Cu3\\n\",\n        \"output\": \" Yes, Zr7Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" B12Mo23Ru15\\n\",\n        \"output\": \" Yes, B12Mo23Ru15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al22Ni3\\n\",\n        \"output\": \" No, Al22Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15V14Co71\\n\",\n        \"output\": \" Yes, Zr15V14Co71 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al88Co7Ni5\\n\",\n        \"output\": \" No, Al88Co7Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd7.5Mg90Ni2.5\\n\",\n        \"output\": \" Yes, Nd7.5Mg90Ni2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe89Cu5B6\\n\",\n        \"output\": \" No, Fe89Cu5B6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7Al89Ni4\\n\",\n        \"output\": \" Yes, La7Al89Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe19B5P\\n\",\n        \"output\": \" Yes, Fe19B5P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si7(Ni24B7)3\\n\",\n        \"output\": \" Yes, Si7(Ni24B7)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe89NiB10\\n\",\n        \"output\": \" No, Fe89NiB10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr18Ti35Cu47\\n\",\n        \"output\": \" Yes, Zr18Ti35Cu47 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg9Ti11Al5\\n\",\n        \"output\": \" No, Mg9Ti11Al5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe14(SiB)3\\n\",\n        \"output\": \" Yes, Fe14(SiB)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe2Ni2B\\n\",\n        \"output\": \" Yes, Fe2Ni2B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni35(Mo2C3)3\\n\",\n        \"output\": \" No, Ni35(Mo2C3)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti38.7Nb10Cu51.3\\n\",\n        \"output\": \" Yes, Ti38.7Nb10Cu51.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al12VGe7\\n\",\n        \"output\": \" No, Al12VGe7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3AlNi\\n\",\n        \"output\": \" Yes, Ti3AlNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn7Co29B14\\n\",\n        \"output\": \" Yes, Mn7Co29B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe5.1Si16.8Pd78.1\\n\",\n        \"output\": \" Yes, Fe5.1Si16.8Pd78.1 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe20B2Mo3\\n\",\n        \"output\": \" No, Fe20B2Mo3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4Ti3Si13\\n\",\n        \"output\": \" Yes, Zr4Ti3Si13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf36.6Nb15Cu48.4\\n\",\n        \"output\": \" Yes, Hf36.6Nb15Cu48.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr14(Al5Ni7)3\\n\",\n        \"output\": \" Yes, Zr14(Al5Ni7)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd7Mg6Cu7\\n\",\n        \"output\": \" Yes, Nd7Mg6Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Fe78.5B18.5\\n\",\n        \"output\": \" Yes, Nd3Fe78.5B18.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al87Ni8\\n\",\n        \"output\": \" Yes, La5Al87Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni29B55C16\\n\",\n        \"output\": \" Yes, Ni29B55C16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg13(Ti9Al20)3\\n\",\n        \"output\": \" No, Mg13(Ti9Al20)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr14Ni7B4\\n\",\n        \"output\": \" Yes, Zr14Ni7B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe31Mo10C9\\n\",\n        \"output\": \" Yes, Fe31Mo10C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2FeCo17\\n\",\n        \"output\": \" Yes, Zr2FeCo17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2Mg5Ag3\\n\",\n        \"output\": \" Yes, Y2Mg5Ag3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10Cr17.1Co72.9\\n\",\n        \"output\": \" Yes, Zr10Cr17.1Co72.9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Al7Ni11\\n\",\n        \"output\": \" Yes, Zr7Al7Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" V5Fe41B4\\n\",\n        \"output\": \" No, V5Fe41B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6CrSi3\\n\",\n        \"output\": \" Yes, Al6CrSi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr6Al3Ni\\n\",\n        \"output\": \" No, Zr6Al3Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7Al3\\n\",\n        \"output\": \" Yes, La7Al3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti42.6Nb1Cu56.4\\n\",\n        \"output\": \" Yes, Ti42.6Nb1Cu56.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" FeCo14B5\\n\",\n        \"output\": \" Yes, FeCo14B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn9Co79B12\\n\",\n        \"output\": \" Yes, Mn9Co79B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ga6Fe77B17\\n\",\n        \"output\": \" Yes, Ga6Fe77B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co70W17.5C12.5\\n\",\n        \"output\": \" No, Co70W17.5C12.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr57.5Cu40B2.5\\n\",\n        \"output\": \" Yes, Zr57.5Cu40B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe65B17.5F17.5\\n\",\n        \"output\": \" Yes, Fe65B17.5F17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr63.65Co5Ni31.35\\n\",\n        \"output\": \" Yes, Zr63.65Co5Ni31.35 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd6Mg11Ni3\\n\",\n        \"output\": \" Yes, Nd6Mg11Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr13(Ni3Mo)3\\n\",\n        \"output\": \" Yes, Cr13(Ni3Mo)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3AlCu\\n\",\n        \"output\": \" Yes, La3AlCu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn3Fe89B8\\n\",\n        \"output\": \" No, Mn3Fe89B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca3Al2\\n\",\n        \"output\": \" Yes, Ca3Al2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg89Al8Ga3\\n\",\n        \"output\": \" No, Mg89Al8Ga3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn23Co53B24\\n\",\n        \"output\": \" Yes, Mn23Co53B24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce5Al44V\\n\",\n        \"output\": \" Yes, Ce5Al44V has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" nail\\n\",\n        \"output\": \" nail is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti13Be7\\n\",\n        \"output\": \" No, Ti13Be7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti67.5Nb15Si17.5\\n\",\n        \"output\": \" Yes, Ti67.5Nb15Si17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2(Al5Ni)3\\n\",\n        \"output\": \" Yes, La2(Al5Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al7VCu2\\n\",\n        \"output\": \" Yes, Al7VCu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrCrCo8\\n\",\n        \"output\": \" Yes, ZrCrCo8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdMg17Cu2\\n\",\n        \"output\": \" Yes, NdMg17Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe80Si12.5B7.5\\n\",\n        \"output\": \" Yes, Fe80Si12.5B7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Cu11\\n\",\n        \"output\": \" Yes, Ti9Cu11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co19Si\\n\",\n        \"output\": \" No, Co19Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2AlCo17\\n\",\n        \"output\": \" Yes, Zr2AlCo17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr65Be32.5Nb2.5\\n\",\n        \"output\": \" Yes, Zr65Be32.5Nb2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7AlNi12\\n\",\n        \"output\": \" Yes, Zr7AlNi12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si18Ag5Pd77\\n\",\n        \"output\": \" Yes, Si18Ag5Pd77 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr67Fe9.9Ni23.1\\n\",\n        \"output\": \" Yes, Zr67Fe9.9Ni23.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Mg13Ni4\\n\",\n        \"output\": \" Yes, Y3Mg13Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg19Mn\\n\",\n        \"output\": \" No, Mg19Mn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La20Al21Ni59\\n\",\n        \"output\": \" Yes, La20Al21Ni59 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni40P9W\\n\",\n        \"output\": \" Yes, Ni40P9W has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Si\\n\",\n        \"output\": \" No, Ti9Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co19B6\\n\",\n        \"output\": \" Yes, Co19B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb3VSi\\n\",\n        \"output\": \" Yes, Nb3VSi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al46Fe3Ni\\n\",\n        \"output\": \" No, Al46Fe3Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf57V28Si15\\n\",\n        \"output\": \" Yes, Hf57V28Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9(Co11W2)7\\n\",\n        \"output\": \" Yes, Zr9(Co11W2)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaAl2Ni7\\n\",\n        \"output\": \" No, LaAl2Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn15(Fe4P)17\\n\",\n        \"output\": \" Yes, Mn15(Fe4P)17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Al23\\n\",\n        \"output\": \" Yes, Nd2Al23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr6.5Fe92B1.5\\n\",\n        \"output\": \" Yes, Zr6.5Fe92B1.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf62V23Si15\\n\",\n        \"output\": \" Yes, Hf62V23Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co81.5B18.5\\n\",\n        \"output\": \" Yes, Co81.5B18.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sm9Al41\\n\",\n        \"output\": \" No, Sm9Al41 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe9(BN)8\\n\",\n        \"output\": \" Yes, Fe9(BN)8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb10Ni73B17\\n\",\n        \"output\": \" Yes, Nb10Ni73B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf12V5Si3\\n\",\n        \"output\": \" Yes, Hf12V5Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al13Ni6Mo\\n\",\n        \"output\": \" Yes, Al13Ni6Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni37B6P7\\n\",\n        \"output\": \" Yes, Ni37B6P7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co77.5Si10B12.5\\n\",\n        \"output\": \" Yes, Co77.5Si10B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce2Cu13Ag10\\n\",\n        \"output\": \" Yes, Ce2Cu13Ag10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti8SiNi\\n\",\n        \"output\": \" Yes, Ti8SiNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al22Fe2Co\\n\",\n        \"output\": \" No, Al22Fe2Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti16P19Pd65\\n\",\n        \"output\": \" Yes, Ti16P19Pd65 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3NiP\\n\",\n        \"output\": \" Yes, Ti3NiP has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al4Co41B5\\n\",\n        \"output\": \" No, Al4Co41B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn19Co65B16\\n\",\n        \"output\": \" Yes, Mn19Co65B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co13Si2B5\\n\",\n        \"output\": \" Yes, Co13Si2B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La8(AlNi3)3\\n\",\n        \"output\": \" Yes, La8(AlNi3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe84SiB15\\n\",\n        \"output\": \" Yes, Fe84SiB15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti13SiNi6\\n\",\n        \"output\": \" Yes, Ti13SiNi6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti61Cu16Ni23\\n\",\n        \"output\": \" Yes, Ti61Cu16Ni23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La7Al10Ni3\\n\",\n        \"output\": \" Yes, La7Al10Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti63Be37\\n\",\n        \"output\": \" Yes, Ti63Be37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" action\\n\",\n        \"output\": \" action is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co16SiC3\\n\",\n        \"output\": \" No, Co16SiC3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn3Si10Pd37\\n\",\n        \"output\": \" Yes, Mn3Si10Pd37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe21Ni21B8\\n\",\n        \"output\": \" Yes, Fe21Ni21B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti39Si11\\n\",\n        \"output\": \" Yes, Ti39Si11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co14(SiB)3\\n\",\n        \"output\": \" Yes, Co14(SiB)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41B9\\n\",\n        \"output\": \" Yes, Fe41B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb9Si4Mo7\\n\",\n        \"output\": \" No, Nb9Si4Mo7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al2Co41B7\\n\",\n        \"output\": \" No, Al2Co41B7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni16P5Pt4\\n\",\n        \"output\": \" Yes, Ni16P5Pt4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" lightning\\n\",\n        \"output\": \" lightning is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" mouse\\n\",\n        \"output\": \" mouse is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Ni13P4\\n\",\n        \"output\": \" Yes, Ti3Ni13P4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Cu3Ni5\\n\",\n        \"output\": \" No, Zr2Cu3Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" eight\\n\",\n        \"output\": \" eight is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Fe88B7\\n\",\n        \"output\": \" No, Zr5Fe88B7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf67Ni33\\n\",\n        \"output\": \" Yes, Hf67Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe71Ni15B14\\n\",\n        \"output\": \" Yes, Fe71Ni15B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y7.5Mg86.5Mn6\\n\",\n        \"output\": \" Yes, Y7.5Mg86.5Mn6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co77W5C18\\n\",\n        \"output\": \" No, Co77W5C18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf4Cu5Ni\\n\",\n        \"output\": \" Yes, Hf4Cu5Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al43Fe3Ni4\\n\",\n        \"output\": \" No, Al43Fe3Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ag20.9Pd62.6\\n\",\n        \"output\": \" No, Si16.5Ag20.9Pd62.6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Al14Ni3\\n\",\n        \"output\": \" No, Zr3Al14Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni\\n\",\n        \"output\": \" No, Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca5La57.5Cu37.5\\n\",\n        \"output\": \" Yes, Ca5La57.5Cu37.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce25Al62.5Fe12.5\\n\",\n        \"output\": \" No, Ce25Al62.5Fe12.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.95Cr33Ni0.05\\n\",\n        \"output\": \" Yes, Zr66.95Cr33Ni0.05 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al87.5Fe2Ni10.5\\n\",\n        \"output\": \" Yes, Al87.5Fe2Ni10.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" V5Co17B3\\n\",\n        \"output\": \" Yes, V5Co17B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti9Al6Ni5\\n\",\n        \"output\": \" Yes, Ti9Al6Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" MnFe17B2\\n\",\n        \"output\": \" No, MnFe17B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti8Si5Ni12\\n\",\n        \"output\": \" Yes, Ti8Si5Ni12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti(Al2Ni)3\\n\",\n        \"output\": \" Yes, Ti(Al2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3Ni7\\n\",\n        \"output\": \" No, Ti3Ni7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf16NbSi3\\n\",\n        \"output\": \" Yes, Hf16NbSi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La11Al5Ag4\\n\",\n        \"output\": \" Yes, La11Al5Ag4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe65B31.5F3.5\\n\",\n        \"output\": \" Yes, Fe65B31.5F3.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe2Cu83Ag15\\n\",\n        \"output\": \" No, Fe2Cu83Ag15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf73(V4Si5)3\\n\",\n        \"output\": \" Yes, Hf73(V4Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SiB2Mo17\\n\",\n        \"output\": \" No, SiB2Mo17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf63V22Si15\\n\",\n        \"output\": \" Yes, Hf63V22Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr(AlNi)2\\n\",\n        \"output\": \" No, Zr(AlNi)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb15Fe2Co83\\n\",\n        \"output\": \" Yes, Nb15Fe2Co83 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co3.5Ni79.5P17\\n\",\n        \"output\": \" No, Co3.5Ni79.5P17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr2(Ge3Pd13)3\\n\",\n        \"output\": \" Yes, Cr2(Ge3Pd13)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni31B19\\n\",\n        \"output\": \" Yes, Ni31B19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si3Ni38B9\\n\",\n        \"output\": \" Yes, Si3Ni38B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti13Al70Ni17\\n\",\n        \"output\": \" Yes, Ti13Al70Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y3Al22\\n\",\n        \"output\": \" Yes, Y3Al22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr8Fe41B\\n\",\n        \"output\": \" No, Cr8Fe41B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr63.65Fe5Ni31.35\\n\",\n        \"output\": \" Yes, Zr63.65Fe5Ni31.35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe93Ni3B4\\n\",\n        \"output\": \" No, Fe93Ni3B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf79(Nb2Si5)3\\n\",\n        \"output\": \" Yes, Hf79(Nb2Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al68Cr15Si17\\n\",\n        \"output\": \" No, Al68Cr15Si17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" output\\n\",\n        \"output\": \" output is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr56Ni39Mo5\\n\",\n        \"output\": \" Yes, Cr56Ni39Mo5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15CuNi4\\n\",\n        \"output\": \" No, Zr15CuNi4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr35Ti11Cu54\\n\",\n        \"output\": \" Yes, Zr35Ti11Cu54 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb3Fe15B2\\n\",\n        \"output\": \" Yes, Nb3Fe15B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al79Si11Ni10\\n\",\n        \"output\": \" Yes, Al79Si11Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni30B13C7\\n\",\n        \"output\": \" Yes, Ni30B13C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Co44Ni\\n\",\n        \"output\": \" Yes, Zr5Co44Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe20B3Mo2\\n\",\n        \"output\": \" Yes, Fe20B3Mo2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al9Cr4Si7\\n\",\n        \"output\": \" No, Al9Cr4Si7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr(Al2Ni)3\\n\",\n        \"output\": \" Yes, Zr(Al2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TaNb7Si2\\n\",\n        \"output\": \" Yes, TaNb7Si2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni22(B3C)7\\n\",\n        \"output\": \" Yes, Ni22(B3C)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3NbAl46\\n\",\n        \"output\": \" Yes, Ce3NbAl46 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Cu5Ni3\\n\",\n        \"output\": \" No, Zr2Cu5Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn17.4Al72.5Si10.1\\n\",\n        \"output\": \" No, Mn17.4Al72.5Si10.1 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5(Fe2Ni3)9\\n\",\n        \"output\": \" Yes, Zr5(Fe2Ni3)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Fe22B\\n\",\n        \"output\": \" Yes, Zr2Fe22B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe78.5P15C6.5\\n\",\n        \"output\": \" Yes, Fe78.5P15C6.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe37Ag63\\n\",\n        \"output\": \" No, Fe37Ag63 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg17Ti60Al23\\n\",\n        \"output\": \" No, Mg17Ti60Al23 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7.3Fe77.5B15.2\\n\",\n        \"output\": \" Yes, Nb7.3Fe77.5B15.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe32.5Ni50.5B17\\n\",\n        \"output\": \" Yes, Fe32.5Ni50.5B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" B5(Mo3Rh7)2\\n\",\n        \"output\": \" Yes, B5(Mo3Rh7)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdMg11Cu8\\n\",\n        \"output\": \" Yes, NdMg11Cu8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ag15Pd68.5\\n\",\n        \"output\": \" Yes, Si16.5Ag15Pd68.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti(AlCu)2\\n\",\n        \"output\": \" No, Ti(AlCu)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe81B14Mo5\\n\",\n        \"output\": \" Yes, Fe81B14Mo5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al8(Co9B5)3\\n\",\n        \"output\": \" Yes, Al8(Co9B5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Si20Pd77\\n\",\n        \"output\": \" Yes, Mn3Si20Pd77 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg4Cu3\\n\",\n        \"output\": \" Yes, Nd3Mg4Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf34.4Nb20Cu45.6\\n\",\n        \"output\": \" Yes, Hf34.4Nb20Cu45.6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Ni7\\n\",\n        \"output\": \" Yes, Zr3Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni39B11\\n\",\n        \"output\": \" No, Ni39B11 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMnAl8\\n\",\n        \"output\": \" No, CeMnAl8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Al4Cu43\\n\",\n        \"output\": \" No, Ce3Al4Cu43 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg5Ni4\\n\",\n        \"output\": \" No, YMg5Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe75B19P6\\n\",\n        \"output\": \" No, Fe75B19P6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Ti2Si\\n\",\n        \"output\": \" Yes, Zr7Ti2Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf77V8Si15\\n\",\n        \"output\": \" Yes, Hf77V8Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr17Al57Ni26\\n\",\n        \"output\": \" Yes, Zr17Al57Ni26 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdMg14Cu5\\n\",\n        \"output\": \" Yes, NdMg14Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co16B5C4\\n\",\n        \"output\": \" Yes, Co16B5C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd3Al22\\n\",\n        \"output\": \" Yes, Gd3Al22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf83V2Si15\\n\",\n        \"output\": \" Yes, Hf83V2Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti13Cu7\\n\",\n        \"output\": \" Yes, Ti13Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" SiNiPd3\\n\",\n        \"output\": \" Yes, SiNiPd3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" growth\\n\",\n        \"output\": \" growth is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si20Ni67.5C12.5\\n\",\n        \"output\": \" Yes, Si20Ni67.5C12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni6P5Pd14\\n\",\n        \"output\": \" Yes, Ni6P5Pd14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti38Nb5Cu57\\n\",\n        \"output\": \" Yes, Ti38Nb5Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti13Si2Ni5\\n\",\n        \"output\": \" Yes, Ti13Si2Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9Fe90B\\n\",\n        \"output\": \" Yes, Zr9Fe90B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti2Co37B11\\n\",\n        \"output\": \" Yes, Ti2Co37B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" V5Co80.75B14.25\\n\",\n        \"output\": \" Yes, V5Co80.75B14.25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti11Ni9\\n\",\n        \"output\": \" Yes, Ti11Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al87.5Fe3.5Ni9\\n\",\n        \"output\": \" Yes, Al87.5Fe3.5Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe39Si5B6\\n\",\n        \"output\": \" Yes, Fe39Si5B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd6Mg9Cu5\\n\",\n        \"output\": \" Yes, Nd6Mg9Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Gd3Al15Ni2\\n\",\n        \"output\": \" No, Gd3Al15Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr51V25Ni24\\n\",\n        \"output\": \" Yes, Zr51V25Ni24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al86CoNi13\\n\",\n        \"output\": \" No, Al86CoNi13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr2.5Fe82.5B15\\n\",\n        \"output\": \" Yes, Cr2.5Fe82.5B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al14(Ni7B5)3\\n\",\n        \"output\": \" No, Al14(Ni7B5)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce(Cu2Ag)3\\n\",\n        \"output\": \" Yes, Ce(Cu2Ag)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe36Cu49Ag15\\n\",\n        \"output\": \" No, Fe36Cu49Ag15 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Co77Mo18\\n\",\n        \"output\": \" Yes, Zr5Co77Mo18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca7.5Al90Fe2.5\\n\",\n        \"output\": \" Yes, Ca7.5Al90Fe2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" temple\\n\",\n        \"output\": \" temple is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15Fe82B3\\n\",\n        \"output\": \" No, Zr15Fe82B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co33B16C\\n\",\n        \"output\": \" Yes, Co33B16C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr67Ti8Si25\\n\",\n        \"output\": \" Yes, Zr67Ti8Si25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al63Si6Mo31\\n\",\n        \"output\": \" Yes, Al63Si6Mo31 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr17Ti8Cu75\\n\",\n        \"output\": \" No, Zr17Ti8Cu75 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si9Pd40Au\\n\",\n        \"output\": \" Yes, Si9Pd40Au has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr97.5Be2.5\\n\",\n        \"output\": \" No, Zr97.5Be2.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiSi4\\n\",\n        \"output\": \" Yes, TiSi4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn21Co51B28\\n\",\n        \"output\": \" Yes, Mn21Co51B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr20(Co7C3)3\\n\",\n        \"output\": \" Yes, Cr20(Co7C3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl8Co\\n\",\n        \"output\": \" Yes, CeAl8Co has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr83AlNi16\\n\",\n        \"output\": \" Yes, Zr83AlNi16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Al23Ni18\\n\",\n        \"output\": \" Yes, La9Al23Ni18 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" catsup\\n\",\n        \"output\": \" catsup is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg4Ag5\\n\",\n        \"output\": \" No, YMg4Ag5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe19B5Mo\\n\",\n        \"output\": \" Yes, Fe19B5Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe75P7.5C17.5\\n\",\n        \"output\": \" Yes, Fe75P7.5C17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" BaLa61Cu38\\n\",\n        \"output\": \" Yes, BaLa61Cu38 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd14Fe82.2B4.8\\n\",\n        \"output\": \" Yes, Nd14Fe82.2B4.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39Ni5B6\\n\",\n        \"output\": \" Yes, Fe39Ni5B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al88(Co3Ni)3\\n\",\n        \"output\": \" No, Al88(Co3Ni)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg8Ag\\n\",\n        \"output\": \" Yes, YMg8Ag has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La2Al2Cu\\n\",\n        \"output\": \" No, La2Al2Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe66.5Co16.5B17\\n\",\n        \"output\": \" Yes, Fe66.5Co16.5B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al10Ni31B9\\n\",\n        \"output\": \" Yes, Al10Ni31B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr18Cu7\\n\",\n        \"output\": \" No, Zr18Cu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdMg2Ni\\n\",\n        \"output\": \" Yes, NdMg2Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiAl5Cu4\\n\",\n        \"output\": \" Yes, TiAl5Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Pr0.3Zr10Fe89.7\\n\",\n        \"output\": \" Yes, Pr0.3Zr10Fe89.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti19Al29Ni52\\n\",\n        \"output\": \" Yes, Ti19Al29Ni52 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti10Al9Cu\\n\",\n        \"output\": \" No, Ti10Al9Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Al16Cu\\n\",\n        \"output\": \" No, Ce3Al16Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr19Fe6\\n\",\n        \"output\": \" Yes, Zr19Fe6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Fe39B8\\n\",\n        \"output\": \" Yes, Zr3Fe39B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sm3Al22\\n\",\n        \"output\": \" Yes, Sm3Al22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca10Al87.5Ni2.5\\n\",\n        \"output\": \" No, Ca10Al87.5Ni2.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg3Ni4\\n\",\n        \"output\": \" Yes, La3Mg3Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti16NbSi3\\n\",\n        \"output\": \" Yes, Ti16NbSi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce5Al44Co\\n\",\n        \"output\": \" Yes, Ce5Al44Co has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Pd79.3Rh4.2\\n\",\n        \"output\": \" Yes, Si16.5Pd79.3Rh4.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe77.5Si15B7.5\\n\",\n        \"output\": \" Yes, Fe77.5Si15B7.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr35Fe11B4\\n\",\n        \"output\": \" Yes, Zr35Fe11B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr50.25Fe25Ni24.75\\n\",\n        \"output\": \" Yes, Zr50.25Fe25Ni24.75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti17Si3\\n\",\n        \"output\": \" Yes, Ti17Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si17.6Pd82.4\\n\",\n        \"output\": \" Yes, Si17.6Pd82.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu3Ni36P11\\n\",\n        \"output\": \" Yes, Cu3Ni36P11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe40Si3P7\\n\",\n        \"output\": \" Yes, Fe40Si3P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al90Fe7\\n\",\n        \"output\": \" Yes, Ce3Al90Fe7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8Ni29B13\\n\",\n        \"output\": \" Yes, Al8Ni29B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43Fe4Co3\\n\",\n        \"output\": \" No, Al43Fe4Co3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41Ni41B18\\n\",\n        \"output\": \" Yes, Fe41Ni41B18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co17(B3C)2\\n\",\n        \"output\": \" Yes, Co17(B3C)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe39B5F6\\n\",\n        \"output\": \" Yes, Fe39B5F6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd9Al81Ni10\\n\",\n        \"output\": \" Yes, Nd9Al81Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn11(Co9B4)3\\n\",\n        \"output\": \" Yes, Mn11(Co9B4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" dress\\n\",\n        \"output\": \" dress is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Co74W13\\n\",\n        \"output\": \" Yes, Zr13Co74W13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al4Co29B17\\n\",\n        \"output\": \" Yes, Al4Co29B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9Ti4Si7\\n\",\n        \"output\": \" Yes, Zr9Ti4Si7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4Ni\\n\",\n        \"output\": \" Yes, La4Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl44Fe5\\n\",\n        \"output\": \" Yes, CeAl44Fe5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe12B7F\\n\",\n        \"output\": \" Yes, Fe12B7F has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7AlNi2\\n\",\n        \"output\": \" Yes, La7AlNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba9(La4Cu3)13\\n\",\n        \"output\": \" Yes, Ba9(La4Cu3)13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al15Co2Si3\\n\",\n        \"output\": \" Yes, Al15Co2Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe87Cu3B10\\n\",\n        \"output\": \" No, Fe87Cu3B10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" environment\\n\",\n        \"output\": \" environment is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti5AlNi4\\n\",\n        \"output\": \" Yes, Ti5AlNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr11(Nb2Ge)3\\n\",\n        \"output\": \" Yes, Zr11(Nb2Ge)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6.5V12Co81.5\\n\",\n        \"output\": \" Yes, Zr6.5V12Co81.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7Al9Ni4\\n\",\n        \"output\": \" Yes, La7Al9Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y6Mg43Mn\\n\",\n        \"output\": \" Yes, Y6Mg43Mn has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5.5Fe92B2.5\\n\",\n        \"output\": \" Yes, Zr5.5Fe92B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg3\\n\",\n        \"output\": \" No, YMg3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co40Si3B7\\n\",\n        \"output\": \" Yes, Co40Si3B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiNb2Si\\n\",\n        \"output\": \" No, TiNb2Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca11Al89\\n\",\n        \"output\": \" Yes, Ca11Al89 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe20Ge2B3\\n\",\n        \"output\": \" Yes, Fe20Ge2B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe38(BMo3)3\\n\",\n        \"output\": \" No, Fe38(BMo3)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf49(Nb12Si5)3\\n\",\n        \"output\": \" Yes, Hf49(Nb12Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf7(Fe29B2)3\\n\",\n        \"output\": \" Yes, Hf7(Fe29B2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al73Fe13Cu14\\n\",\n        \"output\": \" No, Al73Fe13Cu14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al44CoNi5\\n\",\n        \"output\": \" No, Al44CoNi5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni41P18Pd41\\n\",\n        \"output\": \" Yes, Ni41P18Pd41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni6P5Pt14\\n\",\n        \"output\": \" Yes, Ni6P5Pt14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al63Fe12Si25\\n\",\n        \"output\": \" Yes, Al63Fe12Si25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ocelot\\n\",\n        \"output\": \" ocelot is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr35(Ni4P)3\\n\",\n        \"output\": \" Yes, Zr35(Ni4P)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7.1Fe77.9B15\\n\",\n        \"output\": \" Yes, Nb7.1Fe77.9B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Ti4Cu13\\n\",\n        \"output\": \" Yes, Zr3Ti4Cu13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Ni7\\n\",\n        \"output\": \" No, La3Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca8.5La58.5Cu33\\n\",\n        \"output\": \" Yes, Ca8.5La58.5Cu33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Al9Cu8\\n\",\n        \"output\": \" No, Ti3Al9Cu8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Al3\\n\",\n        \"output\": \" No, Ti7Al3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe5Cu16Ag29\\n\",\n        \"output\": \" No, Fe5Cu16Ag29 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti8Al5Cu7\\n\",\n        \"output\": \" Yes, Ti8Al5Cu7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn28Co41B31\\n\",\n        \"output\": \" Yes, Mn28Co41B31 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe43B7\\n\",\n        \"output\": \" Yes, Fe43B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiCu5Ni4\\n\",\n        \"output\": \" No, TiCu5Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr21Ti24Si55\\n\",\n        \"output\": \" Yes, Zr21Ti24Si55 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn18Fe5B2\\n\",\n        \"output\": \" No, Mn18Fe5B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe19B6\\n\",\n        \"output\": \" Yes, Fe19B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni8BP\\n\",\n        \"output\": \" Yes, Ni8BP has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr29Al9Ni62\\n\",\n        \"output\": \" Yes, Zr29Al9Ni62 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn5Fe37B8\\n\",\n        \"output\": \" Yes, Mn5Fe37B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al14VCu5\\n\",\n        \"output\": \" No, Al14VCu5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaMg19Zn5\\n\",\n        \"output\": \" Yes, LaMg19Zn5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81Cu5B14\\n\",\n        \"output\": \" No, Fe81Cu5B14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd3Zr5Fe42\\n\",\n        \"output\": \" No, Gd3Zr5Fe42 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn5Fe83B12\\n\",\n        \"output\": \" No, Mn5Fe83B12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Ti7Si40\\n\",\n        \"output\": \" Yes, Zr3Ti7Si40 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaMg17Ni2\\n\",\n        \"output\": \" Yes, LaMg17Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si22.5Ni67.5C10\\n\",\n        \"output\": \" No, Si22.5Ni67.5C10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe83Si8B9\\n\",\n        \"output\": \" No, Fe83Si8B9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg11Ti14Al25\\n\",\n        \"output\": \" No, Mg11Ti14Al25 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8(Ti3Si)3\\n\",\n        \"output\": \" Yes, Zr8(Ti3Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" sycamore\\n\",\n        \"output\": \" sycamore is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al43Ni4\\n\",\n        \"output\": \" No, Mn3Al43Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" TiAlCu2\\n\",\n        \"output\": \" Yes, TiAlCu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe7Ni7B6\\n\",\n        \"output\": \" Yes, Fe7Ni7B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79(B3P4)3\\n\",\n        \"output\": \" Yes, Fe79(B3P4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg16Al3Zn\\n\",\n        \"output\": \" No, Mg16Al3Zn does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe78Si7.5B14.5\\n\",\n        \"output\": \" Yes, Fe78Si7.5B14.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al6Fe37B7\\n\",\n        \"output\": \" Yes, Al6Fe37B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce6Mn5Al89\\n\",\n        \"output\": \" No, Ce6Mn5Al89 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" HoFe41B8\\n\",\n        \"output\": \" Yes, HoFe41B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg18Ag\\n\",\n        \"output\": \" No, YMg18Ag does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CuNi37P12\\n\",\n        \"output\": \" No, CuNi37P12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2Mg3Cu5\\n\",\n        \"output\": \" Yes, La2Mg3Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al52Si25Ni23\\n\",\n        \"output\": \" Yes, Al52Si25Ni23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf2Cu3\\n\",\n        \"output\": \" Yes, Hf2Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm2Al17Ni\\n\",\n        \"output\": \" Yes, Sm2Al17Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Al2Ni5\\n\",\n        \"output\": \" Yes, Zr3Al2Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" FeNi7P2\\n\",\n        \"output\": \" Yes, FeNi7P2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe13B7\\n\",\n        \"output\": \" Yes, Fe13B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La7Al6Ni7\\n\",\n        \"output\": \" Yes, La7Al6Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al92Fe5Ni3\\n\",\n        \"output\": \" No, Al92Fe5Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La8Al5Ni7\\n\",\n        \"output\": \" Yes, La8Al5Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13Be4Nb3\\n\",\n        \"output\": \" No, Zr13Be4Nb3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43Fe6Si\\n\",\n        \"output\": \" No, Al43Fe6Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce5(Al4Fe)3\\n\",\n        \"output\": \" No, Ce5(Al4Fe)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn15Co61B24\\n\",\n        \"output\": \" Yes, Mn15Co61B24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al4Co31B15\\n\",\n        \"output\": \" Yes, Al4Co31B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni21B25C4\\n\",\n        \"output\": \" No, Ni21B25C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti6(Co3B)11\\n\",\n        \"output\": \" Yes, Ti6(Co3B)11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Ti4Si13\\n\",\n        \"output\": \" Yes, Zr3Ti4Si13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Al15Ni\\n\",\n        \"output\": \" No, Nd4Al15Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Cu2Ni3\\n\",\n        \"output\": \" Yes, Zr5Cu2Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf11TaFe38\\n\",\n        \"output\": \" Yes, Hf11TaFe38 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al17Ni2Mo\\n\",\n        \"output\": \" Yes, Al17Ni2Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co41Si2B7\\n\",\n        \"output\": \" No, Co41Si2B7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si15(Ni4B)17\\n\",\n        \"output\": \" Yes, Si15(Ni4B)17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnAl43Co6\\n\",\n        \"output\": \" No, MnAl43Co6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La2Al3Cu5\\n\",\n        \"output\": \" No, La2Al3Cu5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Mg6Cu\\n\",\n        \"output\": \" No, Y3Mg6Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca8La59.5Cu32.5\\n\",\n        \"output\": \" Yes, Ca8La59.5Cu32.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co9Ni74P17\\n\",\n        \"output\": \" No, Co9Ni74P17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La(Mg2Cu)3\\n\",\n        \"output\": \" Yes, La(Mg2Cu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd4Al45Ni\\n\",\n        \"output\": \" Yes, Nd4Al45Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Ti3Ni5\\n\",\n        \"output\": \" Yes, Zr2Ti3Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe27Cu45Ag28\\n\",\n        \"output\": \" No, Fe27Cu45Ag28 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Al11\\n\",\n        \"output\": \" Yes, La9Al11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm9Al83Ni8\\n\",\n        \"output\": \" Yes, Sm9Al83Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co31Mo10C9\\n\",\n        \"output\": \" Yes, Co31Mo10C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al2VGe\\n\",\n        \"output\": \" No, Al2VGe does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37B10N3\\n\",\n        \"output\": \" Yes, Fe37B10N3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77B17P6\\n\",\n        \"output\": \" Yes, Fe77B17P6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti6SiNi3\\n\",\n        \"output\": \" Yes, Ti6SiNi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr18Ni6P\\n\",\n        \"output\": \" Yes, Zr18Ni6P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe73.5B20W6.5\\n\",\n        \"output\": \" Yes, Fe73.5B20W6.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10Fe22.5Co67.5\\n\",\n        \"output\": \" Yes, Zr10Fe22.5Co67.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg31(Ti18Al5)3\\n\",\n        \"output\": \" No, Mg31(Ti18Al5)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co27Mo12C11\\n\",\n        \"output\": \" Yes, Co27Mo12C11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y3Mg6Ag\\n\",\n        \"output\": \" Yes, Y3Mg6Ag has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni33Mo8C9\\n\",\n        \"output\": \" No, Ni33Mo8C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr73Fe23B4\\n\",\n        \"output\": \" Yes, Zr73Fe23B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La26Al57Ni17\\n\",\n        \"output\": \" Yes, La26Al57Ni17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr38V25Ni37\\n\",\n        \"output\": \" Yes, Zr38V25Ni37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr5Fe43B2\\n\",\n        \"output\": \" Yes, Cr5Fe43B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd6Al39Ni5\\n\",\n        \"output\": \" Yes, Gd6Al39Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co13Mo7C5\\n\",\n        \"output\": \" Yes, Co13Mo7C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al8(Co11B3)3\\n\",\n        \"output\": \" Yes, Al8(Co11B3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10Fe89.91Ge0.09\\n\",\n        \"output\": \" Yes, Zr10Fe89.91Ge0.09 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" quince\\n\",\n        \"output\": \" quince is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr53Ni18Mo29\\n\",\n        \"output\": \" Yes, Cr53Ni18Mo29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al69Ni6Ge25\\n\",\n        \"output\": \" Yes, Al69Ni6Ge25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Nb10Si3\\n\",\n        \"output\": \" Yes, Ti7Nb10Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn3Al13Si4\\n\",\n        \"output\": \" Yes, Mn3Al13Si4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf81Nb4Si15\\n\",\n        \"output\": \" Yes, Hf81Nb4Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr17Cr2Co81\\n\",\n        \"output\": \" Yes, Zr17Cr2Co81 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Fe45B2\\n\",\n        \"output\": \" Yes, Zr3Fe45B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr51Nb40Si9\\n\",\n        \"output\": \" Yes, Zr51Nb40Si9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni81.5B11.1P7.4\\n\",\n        \"output\": \" Yes, Ni81.5B11.1P7.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti12Al5Ni8\\n\",\n        \"output\": \" Yes, Ti12Al5Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr26Ni19Mo5\\n\",\n        \"output\": \" Yes, Cr26Ni19Mo5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8Co41Mo\\n\",\n        \"output\": \" Yes, Zr8Co41Mo has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe83B9Mo8\\n\",\n        \"output\": \" No, Fe83B9Mo8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr7.5Co67.5B25\\n\",\n        \"output\": \" Yes, Cr7.5Co67.5B25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5.5Co86.5Mo8\\n\",\n        \"output\": \" Yes, Zr5.5Co86.5Mo8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr2Co2B\\n\",\n        \"output\": \" Yes, Cr2Co2B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co13W4C3\\n\",\n        \"output\": \" No, Co13W4C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe20Si2P3\\n\",\n        \"output\": \" Yes, Fe20Si2P3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl44Cu5\\n\",\n        \"output\": \" No, CeAl44Cu5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11Cu7B2\\n\",\n        \"output\": \" Yes, Zr11Cu7B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni21B4\\n\",\n        \"output\": \" No, Ni21B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Fe75B22\\n\",\n        \"output\": \" Yes, Zr3Fe75B22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87Fe3Ni10\\n\",\n        \"output\": \" Yes, Al87Fe3Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La7Al6Cu7\\n\",\n        \"output\": \" Yes, La7Al6Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe39Ni42B19\\n\",\n        \"output\": \" Yes, Fe39Ni42B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb12Fe83B5\\n\",\n        \"output\": \" No, Nb12Fe83B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y5Mg89Mn6\\n\",\n        \"output\": \" Yes, Y5Mg89Mn6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co3.5Ni78.5P18\\n\",\n        \"output\": \" Yes, Co3.5Ni78.5P18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba3La56Cu41\\n\",\n        \"output\": \" Yes, Ba3La56Cu41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe91Cu5B4\\n\",\n        \"output\": \" No, Fe91Cu5B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79(W2C)7\\n\",\n        \"output\": \" No, Fe79(W2C)7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Cu5Ni2\\n\",\n        \"output\": \" Yes, Zr3Cu5Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5AlNi44\\n\",\n        \"output\": \" Yes, Zr5AlNi44 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe91CuB8\\n\",\n        \"output\": \" No, Fe91CuB8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr6Fe39B5\\n\",\n        \"output\": \" No, Cr6Fe39B5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdAl7Ni2\\n\",\n        \"output\": \" Yes, NdAl7Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Al2Ni\\n\",\n        \"output\": \" No, Zr2Al2Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe6Co85B9\\n\",\n        \"output\": \" Yes, Fe6Co85B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce4(Cu27Ag5)3\\n\",\n        \"output\": \" No, Ce4(Cu27Ag5)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si5(Ni13B2)3\\n\",\n        \"output\": \" Yes, Si5(Ni13B2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr43Nb40Si17\\n\",\n        \"output\": \" Yes, Zr43Nb40Si17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr8(Fe13B)3\\n\",\n        \"output\": \" No, Cr8(Fe13B)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti33Nb10Cu57\\n\",\n        \"output\": \" Yes, Ti33Nb10Cu57 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9Al9Ni2\\n\",\n        \"output\": \" Yes, Zr9Al9Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La6Al9Ni5\\n\",\n        \"output\": \" Yes, La6Al9Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y4Mg5Ag\\n\",\n        \"output\": \" No, Y4Mg5Ag does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6.2Co89.8W4\\n\",\n        \"output\": \" Yes, Zr6.2Co89.8W4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrCo8Mo\\n\",\n        \"output\": \" Yes, ZrCo8Mo has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe38(Mo3C)3\\n\",\n        \"output\": \" Yes, Fe38(Mo3C)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe42Cu41Ag17\\n\",\n        \"output\": \" No, Fe42Cu41Ag17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4(AlNi)3\\n\",\n        \"output\": \" Yes, La4(AlNi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" VFe15B4\\n\",\n        \"output\": \" Yes, VFe15B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5Mg13Cu2\\n\",\n        \"output\": \" No, Nd5Mg13Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al22Fe3\\n\",\n        \"output\": \" No, Al22Fe3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu2Ag2Ge\\n\",\n        \"output\": \" Yes, Cu2Ag2Ge has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe13Cu47Ag40\\n\",\n        \"output\": \" No, Fe13Cu47Ag40 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2Al23\\n\",\n        \"output\": \" Yes, La2Al23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg19(AlGa)3\\n\",\n        \"output\": \" Yes, Mg19(AlGa)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Cu45.5Au45.5\\n\",\n        \"output\": \" Yes, La9Cu45.5Au45.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd9Al11\\n\",\n        \"output\": \" Yes, Gd9Al11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti12Be5Si3\\n\",\n        \"output\": \" No, Ti12Be5Si3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba5La53Cu42\\n\",\n        \"output\": \" Yes, Ba5La53Cu42 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca2Al17Cu\\n\",\n        \"output\": \" Yes, Ca2Al17Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al5VGe4\\n\",\n        \"output\": \" No, Al5VGe4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" june\\n\",\n        \"output\": \" june is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5(TiSi14)3\\n\",\n        \"output\": \" No, Zr5(TiSi14)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni15B2C3\\n\",\n        \"output\": \" No, Ni15B2C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni68Mo13P19\\n\",\n        \"output\": \" Yes, Ni68Mo13P19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti28.8Nb33Cu38.2\\n\",\n        \"output\": \" Yes, Ti28.8Nb33Cu38.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe75Si4B21\\n\",\n        \"output\": \" Yes, Fe75Si4B21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" latex\\n\",\n        \"output\": \" latex is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr2(Fe5C)3\\n\",\n        \"output\": \" No, Cr2(Fe5C)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TaNi4\\n\",\n        \"output\": \" Yes, TaNi4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni75B17W8\\n\",\n        \"output\": \" Yes, Ni75B17W8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al86FeNi13\\n\",\n        \"output\": \" No, Al86FeNi13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiNi19P5\\n\",\n        \"output\": \" Yes, TiNi19P5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg7Ni2\\n\",\n        \"output\": \" Yes, NdMg7Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Cu32Ag15\\n\",\n        \"output\": \" Yes, Ce3Cu32Ag15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al44FeNi5\\n\",\n        \"output\": \" No, Al44FeNi5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43Fe5Co2\\n\",\n        \"output\": \" No, Al43Fe5Co2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl14Ni5\\n\",\n        \"output\": \" Yes, LaAl14Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe21Cu15Ag14\\n\",\n        \"output\": \" Yes, Fe21Cu15Ag14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr62.5Cu35B2.5\\n\",\n        \"output\": \" Yes, Zr62.5Cu35B2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr61(Nb10Si3)3\\n\",\n        \"output\": \" No, Zr61(Nb10Si3)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10.2V10.6Co79.2\\n\",\n        \"output\": \" Yes, Zr10.2V10.6Co79.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti15(Nb4Si)17\\n\",\n        \"output\": \" Yes, Ti15(Nb4Si)17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" V15Fe73B12\\n\",\n        \"output\": \" No, V15Fe73B12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe80Si9P11\\n\",\n        \"output\": \" Yes, Fe80Si9P11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca3La68.5Cu28.5\\n\",\n        \"output\": \" Yes, Ca3La68.5Cu28.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co80.5Si7B12.5\\n\",\n        \"output\": \" No, Co80.5Si7B12.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si3Ni15B7\\n\",\n        \"output\": \" No, Si3Ni15B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" SiB3Mo16\\n\",\n        \"output\": \" No, SiB3Mo16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe7Si20Pd73\\n\",\n        \"output\": \" Yes, Fe7Si20Pd73 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83B14C3\\n\",\n        \"output\": \" Yes, Fe83B14C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15AlNi4\\n\",\n        \"output\": \" Yes, Zr15AlNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrCo8Ni\\n\",\n        \"output\": \" Yes, ZrCo8Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni81.5B17P1.5\\n\",\n        \"output\": \" Yes, Ni81.5B17P1.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co9Ni72P19\\n\",\n        \"output\": \" Yes, Co9Ni72P19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y3Mg5Ag2\\n\",\n        \"output\": \" Yes, Y3Mg5Ag2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al13Cr4Si3\\n\",\n        \"output\": \" No, Al13Cr4Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr21Al17Ni12\\n\",\n        \"output\": \" Yes, Zr21Al17Ni12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni18B5C2\\n\",\n        \"output\": \" No, Ni18B5C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr3Fe15C2\\n\",\n        \"output\": \" No, Cr3Fe15C2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15Ta2Si3\\n\",\n        \"output\": \" Yes, Zr15Ta2Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu14Si15.1Pd70.9\\n\",\n        \"output\": \" Yes, Cu14Si15.1Pd70.9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca(La5Cu2)7\\n\",\n        \"output\": \" Yes, Ca(La5Cu2)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al8Ni25B17\\n\",\n        \"output\": \" Yes, Al8Ni25B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn4Fe16B5\\n\",\n        \"output\": \" Yes, Mn4Fe16B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr3Co13B4\\n\",\n        \"output\": \" Yes, Cr3Co13B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" cupcake\\n\",\n        \"output\": \" cupcake is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn17.4Al70.6Si12\\n\",\n        \"output\": \" No, Mn17.4Al70.6Si12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La5(AlNi4)3\\n\",\n        \"output\": \" No, La5(AlNi4)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y5Mg13Cu2\\n\",\n        \"output\": \" Yes, Y5Mg13Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb5.3Fe80.2B14.5\\n\",\n        \"output\": \" Yes, Nb5.3Fe80.2B14.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al4Cu\\n\",\n        \"output\": \" No, La5Al4Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg79Cu20\\n\",\n        \"output\": \" Yes, YMg79Cu20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni17C3\\n\",\n        \"output\": \" No, Ni17C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb14Co81B5\\n\",\n        \"output\": \" Yes, Nb14Co81B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn17Co67B16\\n\",\n        \"output\": \" Yes, Mn17Co67B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrAlNi8\\n\",\n        \"output\": \" No, ZrAlNi8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni41B9\\n\",\n        \"output\": \" Yes, Ni41B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaMg15Ni4\\n\",\n        \"output\": \" Yes, LaMg15Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" sock\\n\",\n        \"output\": \" sock is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3BMo16\\n\",\n        \"output\": \" No, Si3BMo16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg19(AlGa2)2\\n\",\n        \"output\": \" Yes, Mg19(AlGa2)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2.5Nb8.5Co89\\n\",\n        \"output\": \" Yes, Zr2.5Nb8.5Co89 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl47Fe2\\n\",\n        \"output\": \" No, CeAl47Fe2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe33Ni5B12\\n\",\n        \"output\": \" Yes, Fe33Ni5B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrFe16B3\\n\",\n        \"output\": \" Yes, ZrFe16B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al82(Fe5Ni)3\\n\",\n        \"output\": \" Yes, Al82(Fe5Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" cell\\n\",\n        \"output\": \" cell is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Ni7\\n\",\n        \"output\": \" No, Nd3Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Mg5Ni\\n\",\n        \"output\": \" No, Nd4Mg5Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe75B18F7\\n\",\n        \"output\": \" Yes, Fe75B18F7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr11Fe74B15\\n\",\n        \"output\": \" Yes, Cr11Fe74B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn6Co11B8\\n\",\n        \"output\": \" Yes, Mn6Co11B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Gd5Al87Ni8\\n\",\n        \"output\": \" Yes, Gd5Al87Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe5Co4\\n\",\n        \"output\": \" Yes, ZrFe5Co4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr66.85Fe33Ni0.15\\n\",\n        \"output\": \" Yes, Zr66.85Fe33Ni0.15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr42Ni31Mo27\\n\",\n        \"output\": \" Yes, Cr42Ni31Mo27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn57Co27B16\\n\",\n        \"output\": \" Yes, Mn57Co27B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe6Ni85B9\\n\",\n        \"output\": \" Yes, Fe6Ni85B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr16Ti3Si\\n\",\n        \"output\": \" Yes, Zr16Ti3Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn43.5Co36.5B20\\n\",\n        \"output\": \" Yes, Mn43.5Co36.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41Si2B7\\n\",\n        \"output\": \" Yes, Fe41Si2B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeMg8Ni\\n\",\n        \"output\": \" Yes, CeMg8Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10(FeNi9)9\\n\",\n        \"output\": \" Yes, Zr10(FeNi9)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39B10Mo\\n\",\n        \"output\": \" Yes, Fe39B10Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83Ni5B12\\n\",\n        \"output\": \" No, Fe83Ni5B12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaAlCu8\\n\",\n        \"output\": \" No, LaAlCu8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu82.5Ag10.5P7\\n\",\n        \"output\": \" Yes, Cu82.5Ag10.5P7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti2Cu5Ni3\\n\",\n        \"output\": \" No, Ti2Cu5Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" pin\\n\",\n        \"output\": \" pin is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Yb20.22Ce25.73Cu54.05\\n\",\n        \"output\": \" Yes, Yb20.22Ce25.73Cu54.05 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb15Fe77B8\\n\",\n        \"output\": \" Yes, Nb15Fe77B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti12Be7Si\\n\",\n        \"output\": \" Yes, Ti12Be7Si has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La13Al83Ni4\\n\",\n        \"output\": \" Yes, La13Al83Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe19CoB5\\n\",\n        \"output\": \" Yes, Fe19CoB5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd12.9Co73Mo14.1\\n\",\n        \"output\": \" Yes, Gd12.9Co73Mo14.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al24Ni\\n\",\n        \"output\": \" No, Al24Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Al7\\n\",\n        \"output\": \" No, La3Al7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" thought\\n\",\n        \"output\": \" thought is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5(Ti4Si)3\\n\",\n        \"output\": \" Yes, Zr5(Ti4Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti11Al72Ni17\\n\",\n        \"output\": \" Yes, Ti11Al72Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnSi10Pd39\\n\",\n        \"output\": \" Yes, MnSi10Pd39 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti2Al7Cu\\n\",\n        \"output\": \" No, Ti2Al7Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" FeNi\\n\",\n        \"output\": \" Yes, FeNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti2Al11Cu7\\n\",\n        \"output\": \" No, Ti2Al11Cu7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti2Cu7Ni\\n\",\n        \"output\": \" No, Ti2Cu7Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti13Al87\\n\",\n        \"output\": \" No, Ti13Al87 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Mg5Cu3\\n\",\n        \"output\": \" Yes, Nd2Mg5Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti10Co76.5B13.5\\n\",\n        \"output\": \" Yes, Ti10Co76.5B13.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B14P5\\n\",\n        \"output\": \" Yes, Fe81B14P5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti10CuNi9\\n\",\n        \"output\": \" No, Ti10CuNi9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf41Nb44Si15\\n\",\n        \"output\": \" Yes, Hf41Nb44Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe15Si2B3\\n\",\n        \"output\": \" Yes, Fe15Si2B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti2Co17B6\\n\",\n        \"output\": \" Yes, Ti2Co17B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y12Al5Cu8\\n\",\n        \"output\": \" Yes, Y12Al5Cu8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni33B11C6\\n\",\n        \"output\": \" Yes, Ni33B11C6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La5Mg2Cu3\\n\",\n        \"output\": \" No, La5Mg2Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Cu52Ag45\\n\",\n        \"output\": \" Yes, Ce3Cu52Ag45 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti8(SiNi3)3\\n\",\n        \"output\": \" Yes, Ti8(SiNi3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb6Fe39B5\\n\",\n        \"output\": \" Yes, Nb6Fe39B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83Cu3B14\\n\",\n        \"output\": \" No, Fe83Cu3B14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La2Mg18Zn5\\n\",\n        \"output\": \" Yes, La2Mg18Zn5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr3Fe13B4\\n\",\n        \"output\": \" Yes, Cr3Fe13B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe84B11C5\\n\",\n        \"output\": \" Yes, Fe84B11C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5(Mg4Ni)3\\n\",\n        \"output\": \" Yes, Nd5(Mg4Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co21Mo20C9\\n\",\n        \"output\": \" No, Co21Mo20C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta2Ni17P\\n\",\n        \"output\": \" Yes, Ta2Ni17P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf68V17Si15\\n\",\n        \"output\": \" Yes, Hf68V17Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co18Mo3C4\\n\",\n        \"output\": \" Yes, Co18Mo3C4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr6Fe79B15\\n\",\n        \"output\": \" Yes, Zr6Fe79B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2Mg7Ni\\n\",\n        \"output\": \" No, Y2Mg7Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si9Pd37Au4\\n\",\n        \"output\": \" Yes, Si9Pd37Au4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr58(Ni9P5)3\\n\",\n        \"output\": \" Yes, Cr58(Ni9P5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg5Ag4\\n\",\n        \"output\": \" Yes, YMg5Ag4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg83Ti17\\n\",\n        \"output\": \" No, Mg83Ti17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr4Fe19B2\\n\",\n        \"output\": \" No, Cr4Fe19B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe20Cu49Ag31\\n\",\n        \"output\": \" No, Fe20Cu49Ag31 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y4Mg15Cu\\n\",\n        \"output\": \" No, Y4Mg15Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ga10Fe73B17\\n\",\n        \"output\": \" Yes, Ga10Fe73B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr75Ni24P\\n\",\n        \"output\": \" Yes, Zr75Ni24P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn(Al6Ni)7\\n\",\n        \"output\": \" No, Mn(Al6Ni)7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co25Mo14C11\\n\",\n        \"output\": \" Yes, Co25Mo14C11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr12.2V12Co75.8\\n\",\n        \"output\": \" Yes, Zr12.2V12Co75.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al81Cr19\\n\",\n        \"output\": \" No, Al81Cr19 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg16Ag\\n\",\n        \"output\": \" Yes, Y3Mg16Ag has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co39B11\\n\",\n        \"output\": \" Yes, Co39B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn11Co11B3\\n\",\n        \"output\": \" Yes, Mn11Co11B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca7.5Mg87.5Cu5\\n\",\n        \"output\": \" Yes, Ca7.5Mg87.5Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe45Cu31Ag24\\n\",\n        \"output\": \" No, Fe45Cu31Ag24 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr25Ni56P19\\n\",\n        \"output\": \" Yes, Cr25Ni56P19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Cu7\\n\",\n        \"output\": \" Yes, Zr3Cu7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" rock\\n\",\n        \"output\": \" rock is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al22FeNi2\\n\",\n        \"output\": \" No, Al22FeNi2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co14B8C3\\n\",\n        \"output\": \" Yes, Co14B8C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr3Fe37B10\\n\",\n        \"output\": \" Yes, Cr3Fe37B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" BMo3\\n\",\n        \"output\": \" No, BMo3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr12Cu7B\\n\",\n        \"output\": \" Yes, Zr12Cu7B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd(AlCu7)3\\n\",\n        \"output\": \" No, Nd(AlCu7)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V5Fe89B6\\n\",\n        \"output\": \" No, V5Fe89B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La5Al2Ni3\\n\",\n        \"output\": \" Yes, La5Al2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La11Al5Pt4\\n\",\n        \"output\": \" Yes, La11Al5Pt4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti11(Be2Si)3\\n\",\n        \"output\": \" No, Ti11(Be2Si)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiNi15P4\\n\",\n        \"output\": \" Yes, TiNi15P4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Cu4Ni3\\n\",\n        \"output\": \" Yes, Ti3Cu4Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8VCu\\n\",\n        \"output\": \" Yes, Al8VCu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr37.5Cu60B2.5\\n\",\n        \"output\": \" Yes, Zr37.5Cu60B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe16W4C5\\n\",\n        \"output\": \" No, Fe16W4C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al19Cr5Ge26\\n\",\n        \"output\": \" Yes, Al19Cr5Ge26 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe78.5B20F1.5\\n\",\n        \"output\": \" Yes, Fe78.5B20F1.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y12.5Mg77.5Mn10\\n\",\n        \"output\": \" No, Y12.5Mg77.5Mn10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5Ge18Pd77\\n\",\n        \"output\": \" Yes, Cr5Ge18Pd77 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti14Al5Cu\\n\",\n        \"output\": \" No, Ti14Al5Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79B17P4\\n\",\n        \"output\": \" Yes, Fe79B17P4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al21(CoNi)2\\n\",\n        \"output\": \" No, Al21(CoNi)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeMg18Cu\\n\",\n        \"output\": \" No, CeMg18Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr2.5Fe77.5B20\\n\",\n        \"output\": \" Yes, Cr2.5Fe77.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr9Fe37B4\\n\",\n        \"output\": \" No, Cr9Fe37B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti16Al9\\n\",\n        \"output\": \" No, Ti16Al9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3B3Mo14\\n\",\n        \"output\": \" Yes, Si3B3Mo14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Al6Cu\\n\",\n        \"output\": \" No, Ti3Al6Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co4Si\\n\",\n        \"output\": \" No, Co4Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe19Ni5B\\n\",\n        \"output\": \" No, Fe19Ni5B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7(Al4Ni5)2\\n\",\n        \"output\": \" Yes, Zr7(Al4Ni5)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Al19Ni22\\n\",\n        \"output\": \" Yes, La9Al19Ni22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr4Fe45B\\n\",\n        \"output\": \" Yes, Cr4Fe45B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SmAl8Ni\\n\",\n        \"output\": \" Yes, SmAl8Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si2(Ni11B5)3\\n\",\n        \"output\": \" No, Si2(Ni11B5)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al47Co\\n\",\n        \"output\": \" No, Mn2Al47Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu4Ni35P11\\n\",\n        \"output\": \" Yes, Cu4Ni35P11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf15Nb2Si3\\n\",\n        \"output\": \" Yes, Hf15Nb2Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe22Cu29Ag49\\n\",\n        \"output\": \" No, Fe22Cu29Ag49 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf57Nb28Si15\\n\",\n        \"output\": \" Yes, Hf57Nb28Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn49(Co13B4)3\\n\",\n        \"output\": \" Yes, Mn49(Co13B4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Al6Ni11\\n\",\n        \"output\": \" No, La3Al6Ni11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La7Al88Ni5\\n\",\n        \"output\": \" Yes, La7Al88Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe16Ni5B4\\n\",\n        \"output\": \" Yes, Fe16Ni5B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg2Cu5\\n\",\n        \"output\": \" Yes, Nd3Mg2Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn5(Fe14B)3\\n\",\n        \"output\": \" No, Mn5(Fe14B)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co16Mo4C5\\n\",\n        \"output\": \" Yes, Co16Mo4C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al62(CrSi)19\\n\",\n        \"output\": \" No, Al62(CrSi)19 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu84Ag9P7\\n\",\n        \"output\": \" Yes, Cu84Ag9P7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mo4P5Ru16\\n\",\n        \"output\": \" Yes, Mo4P5Ru16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg7Ag2\\n\",\n        \"output\": \" Yes, YMg7Ag2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5CuNi4\\n\",\n        \"output\": \" Yes, Zr5CuNi4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al85(FeNi4)3\\n\",\n        \"output\": \" No, Al85(FeNi4)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd4.125Fe78.375B17.5\\n\",\n        \"output\": \" Yes, Nd4.125Fe78.375B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe63Ni20B17\\n\",\n        \"output\": \" Yes, Fe63Ni20B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al10Ni23B17\\n\",\n        \"output\": \" Yes, Al10Ni23B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti4Nb13Si3\\n\",\n        \"output\": \" Yes, Ti4Nb13Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" SiNi8C\\n\",\n        \"output\": \" No, SiNi8C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si2Ni18B5\\n\",\n        \"output\": \" Yes, Si2Ni18B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al17FeNi2\\n\",\n        \"output\": \" No, Al17FeNi2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe20SiP4\\n\",\n        \"output\": \" Yes, Fe20SiP4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co15Si3B2\\n\",\n        \"output\": \" Yes, Co15Si3B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" MnAl44Ni5\\n\",\n        \"output\": \" Yes, MnAl44Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2AlNi7\\n\",\n        \"output\": \" No, Zr2AlNi7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni36.5P27Pd36.5\\n\",\n        \"output\": \" Yes, Ni36.5P27Pd36.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al65Si19Ni16\\n\",\n        \"output\": \" Yes, Al65Si19Ni16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb77Si10Ge13\\n\",\n        \"output\": \" Yes, Nb77Si10Ge13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe42SiB7\\n\",\n        \"output\": \" Yes, Fe42SiB7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13Be5Nb2\\n\",\n        \"output\": \" No, Zr13Be5Nb2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti9Nb8Si3\\n\",\n        \"output\": \" Yes, Ti9Nb8Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe40SiP9\\n\",\n        \"output\": \" Yes, Fe40SiP9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al21FeNi3\\n\",\n        \"output\": \" No, Al21FeNi3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd33Fe67\\n\",\n        \"output\": \" Yes, Nd33Fe67 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3AlCu46\\n\",\n        \"output\": \" No, Ce3AlCu46 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg11Cu8\\n\",\n        \"output\": \" Yes, YMg11Cu8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" V9Fe74P17\\n\",\n        \"output\": \" Yes, V9Fe74P17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3AlCu46\\n\",\n        \"output\": \" No, Nd3AlCu46 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe77Ni15B8\\n\",\n        \"output\": \" No, Fe77Ni15B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe57Cu6Ag37\\n\",\n        \"output\": \" No, Fe57Cu6Ag37 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr7(Fe26B5)3\\n\",\n        \"output\": \" Yes, Cr7(Fe26B5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd11Al5Ni4\\n\",\n        \"output\": \" Yes, Nd11Al5Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" tachometer\\n\",\n        \"output\": \" tachometer is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2Cu3\\n\",\n        \"output\": \" No, Nd2Cu3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe75.3Si9.7B15\\n\",\n        \"output\": \" Yes, Fe75.3Si9.7B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca2.5Al92.5Fe5\\n\",\n        \"output\": \" No, Ca2.5Al92.5Fe5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Ni2\\n\",\n        \"output\": \" Yes, Zr3Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb13Co77B10\\n\",\n        \"output\": \" Yes, Nb13Co77B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La13Al2Ni5\\n\",\n        \"output\": \" Yes, La13Al2Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al69Co6Ge25\\n\",\n        \"output\": \" Yes, Al69Co6Ge25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" file\\n\",\n        \"output\": \" file is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si7Ni38B5\\n\",\n        \"output\": \" Yes, Si7Ni38B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Al14Ni27\\n\",\n        \"output\": \" Yes, La9Al14Ni27 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe58.5Ni20B21.5\\n\",\n        \"output\": \" Yes, Fe58.5Ni20B21.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2.5Al87Ni10.5\\n\",\n        \"output\": \" Yes, Mn2.5Al87Ni10.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn3Al40Ni7\\n\",\n        \"output\": \" No, Mn3Al40Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg8Ni\\n\",\n        \"output\": \" Yes, YMg8Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb2Co20B3\\n\",\n        \"output\": \" Yes, Nb2Co20B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ni26.7Pd56.8\\n\",\n        \"output\": \" Yes, Si16.5Ni26.7Pd56.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y57Al5Cu38\\n\",\n        \"output\": \" Yes, Y57Al5Cu38 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrNi\\n\",\n        \"output\": \" Yes, ZrNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Cu4Ni\\n\",\n        \"output\": \" Yes, Zr5Cu4Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn5(Co3B2)4\\n\",\n        \"output\": \" Yes, Mn5(Co3B2)4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2(AlNi5)3\\n\",\n        \"output\": \" No, Zr2(AlNi5)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co16W5C4\\n\",\n        \"output\": \" No, Co16W5C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr39Ti11\\n\",\n        \"output\": \" Yes, Zr39Ti11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La13(Al25Ni4)3\\n\",\n        \"output\": \" Yes, La13(Al25Ni4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Fe83B14\\n\",\n        \"output\": \" Yes, Mn3Fe83B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5Fe44B\\n\",\n        \"output\": \" Yes, Cr5Fe44B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Ti10Si3\\n\",\n        \"output\": \" Yes, Zr7Ti10Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf5CuNi4\\n\",\n        \"output\": \" Yes, Hf5CuNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ferry\\n\",\n        \"output\": \" ferry is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" south\\n\",\n        \"output\": \" south is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf54Nb31Si15\\n\",\n        \"output\": \" Yes, Hf54Nb31Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr5Fe79B16\\n\",\n        \"output\": \" Yes, Cr5Fe79B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAl3Ni\\n\",\n        \"output\": \" Yes, LaAl3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe14(SiC)3\\n\",\n        \"output\": \" Yes, Fe14(SiC)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce13Al87\\n\",\n        \"output\": \" Yes, Ce13Al87 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Sr2La71Cu27\\n\",\n        \"output\": \" Yes, Sr2La71Cu27 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" SiBMo3\\n\",\n        \"output\": \" No, SiBMo3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al63Cr15Si22\\n\",\n        \"output\": \" No, Al63Cr15Si22 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5Ni3P2\\n\",\n        \"output\": \" Yes, Cr5Ni3P2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf11(Cu2Ni)3\\n\",\n        \"output\": \" Yes, Hf11(Cu2Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Mg4Ni3\\n\",\n        \"output\": \" No, Ce3Mg4Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7.5V6Co86.5\\n\",\n        \"output\": \" Yes, Zr7.5V6Co86.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe16GeB3\\n\",\n        \"output\": \" Yes, Fe16GeB3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe19(B2Mo)2\\n\",\n        \"output\": \" Yes, Fe19(B2Mo)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" vegetable\\n\",\n        \"output\": \" vegetable is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al6Co37B7\\n\",\n        \"output\": \" No, Al6Co37B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe43Cu5B2\\n\",\n        \"output\": \" No, Fe43Cu5B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg18Ni\\n\",\n        \"output\": \" No, YMg18Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn5(Fe13B2)3\\n\",\n        \"output\": \" No, Mn5(Fe13B2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Tb3Al\\n\",\n        \"output\": \" Yes, Tb3Al has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl37Ni12\\n\",\n        \"output\": \" Yes, LaAl37Ni12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce6Cu59Ag35\\n\",\n        \"output\": \" Yes, Ce6Cu59Ag35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5Al87Ni8\\n\",\n        \"output\": \" Yes, Nd5Al87Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al43Ni5\\n\",\n        \"output\": \" Yes, Ce2Al43Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y3Mg3Cu4\\n\",\n        \"output\": \" Yes, Y3Mg3Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca6Mg3Ga\\n\",\n        \"output\": \" Yes, Ca6Mg3Ga has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe35(Si3B2)3\\n\",\n        \"output\": \" Yes, Fe35(Si3B2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu4Si9Pd37\\n\",\n        \"output\": \" Yes, Cu4Si9Pd37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9Cu7Ni4\\n\",\n        \"output\": \" Yes, Zr9Cu7Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ag4Pd79.5\\n\",\n        \"output\": \" Yes, Si16.5Ag4Pd79.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr3Fe5B2\\n\",\n        \"output\": \" Yes, Cr3Fe5B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf84NbSi15\\n\",\n        \"output\": \" Yes, Hf84NbSi15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2Mg5Ni3\\n\",\n        \"output\": \" Yes, Ce2Mg5Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sr7La56Cu37\\n\",\n        \"output\": \" Yes, Sr7La56Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti22Al43Ni35\\n\",\n        \"output\": \" Yes, Ti22Al43Ni35 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Cu68.25Au22.75\\n\",\n        \"output\": \" Yes, La9Cu68.25Au22.75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5Mg8Ni7\\n\",\n        \"output\": \" Yes, Nd5Mg8Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr19Ti11Si70\\n\",\n        \"output\": \" Yes, Zr19Ti11Si70 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe95NiB4\\n\",\n        \"output\": \" No, Fe95NiB4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al91CoNi8\\n\",\n        \"output\": \" No, Al91CoNi8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SiNi18C\\n\",\n        \"output\": \" No, SiNi18C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4Mg13Ni3\\n\",\n        \"output\": \" Yes, La4Mg13Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe18Si4B3\\n\",\n        \"output\": \" Yes, Fe18Si4B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr14Fe29C7\\n\",\n        \"output\": \" No, Cr14Fe29C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce8Nb5Al87\\n\",\n        \"output\": \" Yes, Ce8Nb5Al87 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr16.3Co79.7Mo4\\n\",\n        \"output\": \" Yes, Zr16.3Co79.7Mo4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al4Ni31B15\\n\",\n        \"output\": \" Yes, Al4Ni31B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti12Al3Cu5\\n\",\n        \"output\": \" Yes, Ti12Al3Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al10Ni29B11\\n\",\n        \"output\": \" Yes, Al10Ni29B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Ni2\\n\",\n        \"output\": \" Yes, La3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf4Ta31Fe65\\n\",\n        \"output\": \" Yes, Hf4Ta31Fe65 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe21Ni59B20\\n\",\n        \"output\": \" Yes, Fe21Ni59B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13Al2Ni5\\n\",\n        \"output\": \" Yes, Zr13Al2Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe20(Ni7B3)3\\n\",\n        \"output\": \" Yes, Fe20(Ni7B3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti18Fe3Si4\\n\",\n        \"output\": \" Yes, Ti18Fe3Si4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr11Fe89\\n\",\n        \"output\": \" Yes, Zr11Fe89 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr12AlNi7\\n\",\n        \"output\": \" Yes, Zr12AlNi7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti11Cu9\\n\",\n        \"output\": \" Yes, Ti11Cu9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al29Cr10Si11\\n\",\n        \"output\": \" No, Al29Cr10Si11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4Co21\\n\",\n        \"output\": \" Yes, Zr4Co21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co7Ni76P17\\n\",\n        \"output\": \" No, Co7Ni76P17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79(B6P)3\\n\",\n        \"output\": \" No, Fe79(B6P)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si3Ni17B5\\n\",\n        \"output\": \" Yes, Si3Ni17B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al34Cr5Si11\\n\",\n        \"output\": \" Yes, Al34Cr5Si11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co18B4C3\\n\",\n        \"output\": \" Yes, Co18B4C3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb5Fe92B3\\n\",\n        \"output\": \" No, Nb5Fe92B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si2(Ni5C)3\\n\",\n        \"output\": \" No, Si2(Ni5C)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Al14Fe3\\n\",\n        \"output\": \" No, Ce3Al14Fe3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti14(NbSi)3\\n\",\n        \"output\": \" Yes, Ti14(NbSi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La4Mg9Ni7\\n\",\n        \"output\": \" Yes, La4Mg9Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe78.5Si9B12.5\\n\",\n        \"output\": \" Yes, Fe78.5Si9B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Tb5Fe77B18\\n\",\n        \"output\": \" Yes, Tb5Fe77B18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni42B7C\\n\",\n        \"output\": \" No, Ni42B7C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr42AlNi7\\n\",\n        \"output\": \" Yes, Zr42AlNi7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca3AlGa\\n\",\n        \"output\": \" Yes, Ca3AlGa has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si(Ni3B)6\\n\",\n        \"output\": \" Yes, Si(Ni3B)6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba10La53.5Cu36.5\\n\",\n        \"output\": \" Yes, Ba10La53.5Cu36.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Ge3Mo4\\n\",\n        \"output\": \" Yes, Zr13Ge3Mo4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al91(FeNi2)3\\n\",\n        \"output\": \" No, Al91(FeNi2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca1.5La71Cu27.5\\n\",\n        \"output\": \" Yes, Ca1.5La71Cu27.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr35Fe14Rh\\n\",\n        \"output\": \" Yes, Zr35Fe14Rh has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce4Cu61Ag35\\n\",\n        \"output\": \" Yes, Ce4Cu61Ag35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Fe81B16\\n\",\n        \"output\": \" Yes, La3Fe81B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al18CoNi\\n\",\n        \"output\": \" No, Al18CoNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr27V20Ni53\\n\",\n        \"output\": \" Yes, Zr27V20Ni53 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti40.9Nb5Cu54.1\\n\",\n        \"output\": \" Yes, Ti40.9Nb5Cu54.1 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CoNi40P9\\n\",\n        \"output\": \" Yes, CoNi40P9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si13(GePd28)3\\n\",\n        \"output\": \" Yes, Si13(GePd28)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr22.5Cu75B2.5\\n\",\n        \"output\": \" No, Zr22.5Cu75B2.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe38B7Mo5\\n\",\n        \"output\": \" Yes, Fe38B7Mo5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni53B41C6\\n\",\n        \"output\": \" No, Ni53B41C6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg2Ti53Al45\\n\",\n        \"output\": \" Yes, Mg2Ti53Al45 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La21AlNi28\\n\",\n        \"output\": \" Yes, La21AlNi28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al61Cr10Ge29\\n\",\n        \"output\": \" Yes, Al61Cr10Ge29 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Fe22\\n\",\n        \"output\": \" Yes, Zr3Fe22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd8.25Fe74.25B17.5\\n\",\n        \"output\": \" Yes, Nd8.25Fe74.25B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg13Al2Ag5\\n\",\n        \"output\": \" Yes, Mg13Al2Ag5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si4Ni39B7\\n\",\n        \"output\": \" Yes, Si4Ni39B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti9V8Si3\\n\",\n        \"output\": \" Yes, Ti9V8Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" sex\\n\",\n        \"output\": \" sex is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La49AlNi50\\n\",\n        \"output\": \" Yes, La49AlNi50 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al12Co27B11\\n\",\n        \"output\": \" No, Al12Co27B11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf46(Nb13Si5)3\\n\",\n        \"output\": \" Yes, Hf46(Nb13Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" GdAl3Ni\\n\",\n        \"output\": \" No, GdAl3Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAlCu2\\n\",\n        \"output\": \" No, MnAlCu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co16Ni65P19\\n\",\n        \"output\": \" No, Co16Ni65P19 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La14Al69Ni17\\n\",\n        \"output\": \" Yes, La14Al69Ni17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr5Co3B2\\n\",\n        \"output\": \" Yes, Cr5Co3B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg2AlZn2\\n\",\n        \"output\": \" No, Mg2AlZn2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd6.4Al87.2Fe6.4\\n\",\n        \"output\": \" Yes, Gd6.4Al87.2Fe6.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr(CuNi)2\\n\",\n        \"output\": \" No, Zr(CuNi)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co18B6C\\n\",\n        \"output\": \" Yes, Co18B6C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe32W7C11\\n\",\n        \"output\": \" Yes, Fe32W7C11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11(Al2Ni)3\\n\",\n        \"output\": \" Yes, Zr11(Al2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al44Cr5Si\\n\",\n        \"output\": \" No, Al44Cr5Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y2Al5Ni3\\n\",\n        \"output\": \" Yes, Y2Al5Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Mg6Ni\\n\",\n        \"output\": \" No, La3Mg6Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti4Si5Ni16\\n\",\n        \"output\": \" Yes, Ti4Si5Ni16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti16Si5Ni4\\n\",\n        \"output\": \" Yes, Ti16Si5Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr17Ti13Si20\\n\",\n        \"output\": \" Yes, Zr17Ti13Si20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9SiNi10\\n\",\n        \"output\": \" No, Ti9SiNi10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8(CrNi3)3\\n\",\n        \"output\": \" Yes, Zr8(CrNi3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15Al57Ni28\\n\",\n        \"output\": \" Yes, Zr15Al57Ni28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si3Ni36B11\\n\",\n        \"output\": \" Yes, Si3Ni36B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Mg15Ni2\\n\",\n        \"output\": \" Yes, La3Mg15Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8Co37B5\\n\",\n        \"output\": \" No, Al8Co37B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe82SiB17\\n\",\n        \"output\": \" Yes, Fe82SiB17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Al7Cu40\\n\",\n        \"output\": \" No, Nd3Al7Cu40 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43Fe6Ni\\n\",\n        \"output\": \" No, Al43Fe6Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf9Cu6Ni5\\n\",\n        \"output\": \" Yes, Hf9Cu6Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd7Mg8Ni5\\n\",\n        \"output\": \" Yes, Nd7Mg8Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu13(Ni22P7)3\\n\",\n        \"output\": \" No, Cu13(Ni22P7)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3Be2\\n\",\n        \"output\": \" Yes, Ti3Be2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Al16Ni\\n\",\n        \"output\": \" No, Nd3Al16Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" temperature\\n\",\n        \"output\": \" temperature is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe6.7Si16.5Pd76.8\\n\",\n        \"output\": \" Yes, Fe6.7Si16.5Pd76.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4Ti11Si35\\n\",\n        \"output\": \" Yes, Zr4Ti11Si35 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr5(Fe4B)3\\n\",\n        \"output\": \" Yes, Cr5(Fe4B)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Co15W2\\n\",\n        \"output\": \" Yes, Zr3Co15W2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" balance\\n\",\n        \"output\": \" balance is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe77B8Mo15\\n\",\n        \"output\": \" No, Fe77B8Mo15 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd5Al37Ni8\\n\",\n        \"output\": \" Yes, Gd5Al37Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe21Ni62.5B16.5\\n\",\n        \"output\": \" Yes, Fe21Ni62.5B16.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni21B21C8\\n\",\n        \"output\": \" Yes, Ni21B21C8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce5MnAl44\\n\",\n        \"output\": \" Yes, Ce5MnAl44 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr30Ni51P19\\n\",\n        \"output\": \" Yes, Cr30Ni51P19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni33B55C12\\n\",\n        \"output\": \" Yes, Ni33B55C12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf4CuNi5\\n\",\n        \"output\": \" Yes, Hf4CuNi5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn10Al73Ge17\\n\",\n        \"output\": \" Yes, Mn10Al73Ge17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu3Si17Pd80\\n\",\n        \"output\": \" Yes, Cu3Si17Pd80 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41B4Mo5\\n\",\n        \"output\": \" No, Fe41B4Mo5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ni20.9Pd62.6\\n\",\n        \"output\": \" Yes, Si16.5Ni20.9Pd62.6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co15(Mo3C2)2\\n\",\n        \"output\": \" Yes, Co15(Mo3C2)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu80.3Ag12.2P7.5\\n\",\n        \"output\": \" Yes, Cu80.3Ag12.2P7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si18Ni8.2Pd73.8\\n\",\n        \"output\": \" Yes, Si18Ni8.2Pd73.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2Mg5Cu3\\n\",\n        \"output\": \" Yes, La2Mg5Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb5(Co14B)3\\n\",\n        \"output\": \" No, Nb5(Co14B)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La8Al7Ni5\\n\",\n        \"output\": \" Yes, La8Al7Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al6Co31B13\\n\",\n        \"output\": \" Yes, Al6Co31B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrFe17B2\\n\",\n        \"output\": \" Yes, ZrFe17B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Al7Ni\\n\",\n        \"output\": \" No, Ce2Al7Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr11(Co10C3)3\\n\",\n        \"output\": \" No, Cr11(Co10C3)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La(Al2Ni)3\\n\",\n        \"output\": \" No, La(Al2Ni)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe13Si3B4\\n\",\n        \"output\": \" Yes, Fe13Si3B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11Al2Ni7\\n\",\n        \"output\": \" Yes, Zr11Al2Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si2BMo7\\n\",\n        \"output\": \" Yes, Si2BMo7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al2(Ni9B7)3\\n\",\n        \"output\": \" Yes, Al2(Ni9B7)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79.5Si3.5B17\\n\",\n        \"output\": \" Yes, Fe79.5Si3.5B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrAl16Ni3\\n\",\n        \"output\": \" Yes, ZrAl16Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Al82Ni13\\n\",\n        \"output\": \" Yes, Zr5Al82Ni13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Dy44Zr5Fe\\n\",\n        \"output\": \" Yes, Dy44Zr5Fe has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Fe4Si13\\n\",\n        \"output\": \" Yes, Zr3Fe4Si13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf13Ta17Fe70\\n\",\n        \"output\": \" Yes, Hf13Ta17Fe70 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La5(Al3Ni2)3\\n\",\n        \"output\": \" Yes, La5(Al3Ni2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2Al23\\n\",\n        \"output\": \" Yes, Y2Al23 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr8La55Cu37\\n\",\n        \"output\": \" Yes, Sr8La55Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9Al3Ni8\\n\",\n        \"output\": \" Yes, Zr9Al3Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr14FeB5\\n\",\n        \"output\": \" Yes, Cr14FeB5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al52Fe23Si25\\n\",\n        \"output\": \" Yes, Al52Fe23Si25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe73(B4Mo5)3\\n\",\n        \"output\": \" Yes, Fe73(B4Mo5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf67(Ni9P2)3\\n\",\n        \"output\": \" Yes, Hf67(Ni9P2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" dancer\\n\",\n        \"output\": \" dancer is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg16Cu3\\n\",\n        \"output\": \" Yes, YMg16Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti40Al43Ni17\\n\",\n        \"output\": \" Yes, Ti40Al43Ni17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6(AlNi)7\\n\",\n        \"output\": \" Yes, Zr6(AlNi)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al45Fe3Co2\\n\",\n        \"output\": \" No, Al45Fe3Co2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La(MgNi)2\\n\",\n        \"output\": \" Yes, La(MgNi)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg18Al25Pd7\\n\",\n        \"output\": \" No, Mg18Al25Pd7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2NbAl17\\n\",\n        \"output\": \" Yes, Ce2NbAl17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83Cu5B12\\n\",\n        \"output\": \" No, Fe83Cu5B12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Al5Ni2\\n\",\n        \"output\": \" Yes, Zr13Al5Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr43.5Ni40.5P16\\n\",\n        \"output\": \" Yes, Cr43.5Ni40.5P16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co80B7P13\\n\",\n        \"output\": \" Yes, Co80B7P13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Al59Ni32\\n\",\n        \"output\": \" Yes, Zr9Al59Ni32 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" plasterboard\\n\",\n        \"output\": \" plasterboard is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" MnFe91B8\\n\",\n        \"output\": \" No, MnFe91B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe17CuB2\\n\",\n        \"output\": \" No, Fe17CuB2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Cr2Fe43\\n\",\n        \"output\": \" Yes, Zr5Cr2Fe43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr8CrNi11\\n\",\n        \"output\": \" Yes, Zr8CrNi11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co17B7C\\n\",\n        \"output\": \" Yes, Co17B7C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Co17Mo\\n\",\n        \"output\": \" Yes, Zr2Co17Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co75Si7.5B17.5\\n\",\n        \"output\": \" Yes, Co75Si7.5B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr67Fe33\\n\",\n        \"output\": \" Yes, Zr67Fe33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co7(Ni24P7)3\\n\",\n        \"output\": \" Yes, Co7(Ni24P7)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr63.65Cu5Ni31.35\\n\",\n        \"output\": \" Yes, Zr63.65Cu5Ni31.35 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co9Si\\n\",\n        \"output\": \" No, Co9Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al47Fe2Co\\n\",\n        \"output\": \" No, Al47Fe2Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe70Si13B17\\n\",\n        \"output\": \" Yes, Fe70Si13B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr7Ni73P20\\n\",\n        \"output\": \" Yes, Cr7Ni73P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V5Fe91B4\\n\",\n        \"output\": \" No, V5Fe91B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni25B21C4\\n\",\n        \"output\": \" Yes, Ni25B21C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeCu10Ag9\\n\",\n        \"output\": \" Yes, CeCu10Ag9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti6Co35B9\\n\",\n        \"output\": \" Yes, Ti6Co35B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al31Ni14\\n\",\n        \"output\": \" Yes, La5Al31Ni14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti48Al45Ni7\\n\",\n        \"output\": \" Yes, Ti48Al45Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe77.5P10C12.5\\n\",\n        \"output\": \" Yes, Fe77.5P10C12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti6(CuNi)7\\n\",\n        \"output\": \" No, Ti6(CuNi)7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al89Ni9\\n\",\n        \"output\": \" No, Mn2Al89Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La20AlNi29\\n\",\n        \"output\": \" Yes, La20AlNi29 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La17AlNi2\\n\",\n        \"output\": \" Yes, La17AlNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr31Ti4Si15\\n\",\n        \"output\": \" Yes, Zr31Ti4Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Tb28.3Al15Fe56.7\\n\",\n        \"output\": \" No, Tb28.3Al15Fe56.7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co25Mo16C9\\n\",\n        \"output\": \" Yes, Co25Mo16C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe17B2Mo\\n\",\n        \"output\": \" No, Fe17B2Mo does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiCu8Ni\\n\",\n        \"output\": \" No, TiCu8Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al15Ni4Mo\\n\",\n        \"output\": \" Yes, Al15Ni4Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4Al21\\n\",\n        \"output\": \" No, Ti4Al21 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Co43B2\\n\",\n        \"output\": \" Yes, Zr5Co43B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La9(Mg5Ni3)2\\n\",\n        \"output\": \" Yes, La9(Mg5Ni3)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y8Al87Ni5\\n\",\n        \"output\": \" Yes, Y8Al87Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd(Al10Ni)9\\n\",\n        \"output\": \" No, Nd(Al10Ni)9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr2Fe2B\\n\",\n        \"output\": \" Yes, Cr2Fe2B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" eagle\\n\",\n        \"output\": \" eagle is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83NiB16\\n\",\n        \"output\": \" Yes, Fe83NiB16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni66.5B17W16.5\\n\",\n        \"output\": \" Yes, Ni66.5B17W16.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr27Ni8Mo15\\n\",\n        \"output\": \" Yes, Cr27Ni8Mo15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti62.5Be37.5\\n\",\n        \"output\": \" Yes, Ti62.5Be37.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg8Cu\\n\",\n        \"output\": \" Yes, YMg8Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr18Fe23C9\\n\",\n        \"output\": \" Yes, Cr18Fe23C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si14Ni69B17\\n\",\n        \"output\": \" Yes, Si14Ni69B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Ni\\n\",\n        \"output\": \" No, La9Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe50Ni33B17\\n\",\n        \"output\": \" Yes, Fe50Ni33B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" peony\\n\",\n        \"output\": \" peony is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe67.5Si17.5B15\\n\",\n        \"output\": \" Yes, Fe67.5Si17.5B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4Al31Ni15\\n\",\n        \"output\": \" Yes, Zr4Al31Ni15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd6Fe41B3\\n\",\n        \"output\": \" Yes, Nd6Fe41B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn7Co61B32\\n\",\n        \"output\": \" Yes, Mn7Co61B32 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm9Al81Ni10\\n\",\n        \"output\": \" Yes, Sm9Al81Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe85.5Cu0.5B14\\n\",\n        \"output\": \" Yes, Fe85.5Cu0.5B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3Ni13B4\\n\",\n        \"output\": \" Yes, Si3Ni13B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb13Si4Mo3\\n\",\n        \"output\": \" Yes, Nb13Si4Mo3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn7Fe2B\\n\",\n        \"output\": \" No, Mn7Fe2B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4AlNi5\\n\",\n        \"output\": \" Yes, Zr4AlNi5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4Ti\\n\",\n        \"output\": \" Yes, Zr4Ti has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe60.1Ni16.9B23\\n\",\n        \"output\": \" Yes, Fe60.1Ni16.9B23 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe45BMo4\\n\",\n        \"output\": \" No, Fe45BMo4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr7Fe40B3\\n\",\n        \"output\": \" No, Cr7Fe40B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al7Ni2Mo\\n\",\n        \"output\": \" Yes, Al7Ni2Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La8AlNi\\n\",\n        \"output\": \" Yes, La8AlNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16Pd80.5Au3.5\\n\",\n        \"output\": \" Yes, Si16Pd80.5Au3.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" TiAl3Cu\\n\",\n        \"output\": \" No, TiAl3Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2CuNi2\\n\",\n        \"output\": \" Yes, Zr2CuNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn16(Co2B)3\\n\",\n        \"output\": \" Yes, Mn16(Co2B)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd(AlCu11)2\\n\",\n        \"output\": \" No, Nd(AlCu11)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeCu17Ag2\\n\",\n        \"output\": \" No, CeCu17Ag2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiBe\\n\",\n        \"output\": \" No, TiBe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl3Fe\\n\",\n        \"output\": \" No, CeAl3Fe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Cu3\\n\",\n        \"output\": \" Yes, Zr2Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr15Fe26C9\\n\",\n        \"output\": \" Yes, Cr15Fe26C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaMg15Cu4\\n\",\n        \"output\": \" Yes, LaMg15Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf66Nb19Si15\\n\",\n        \"output\": \" Yes, Hf66Nb19Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2(Ni13B3)3\\n\",\n        \"output\": \" Yes, Al2(Ni13B3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm7Al85Ni8\\n\",\n        \"output\": \" Yes, Sm7Al85Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2AlCu7\\n\",\n        \"output\": \" No, Ti2AlCu7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sb19.3Pb27.5Au53.2\\n\",\n        \"output\": \" Yes, Sb19.3Pb27.5Au53.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr53.6Ti20Ni26.4\\n\",\n        \"output\": \" Yes, Zr53.6Ti20Ni26.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb15Fe3.5Co81.5\\n\",\n        \"output\": \" Yes, Nb15Fe3.5Co81.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al87FeNi12\\n\",\n        \"output\": \" Yes, Al87FeNi12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr6Fe11B3\\n\",\n        \"output\": \" Yes, Cr6Fe11B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd9Al81Ni10\\n\",\n        \"output\": \" Yes, Gd9Al81Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11Cu14\\n\",\n        \"output\": \" Yes, Zr11Cu14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Al2Cu45\\n\",\n        \"output\": \" No, Nd3Al2Cu45 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe18B2Mo5\\n\",\n        \"output\": \" No, Fe18B2Mo5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrAl14Ni5\\n\",\n        \"output\": \" No, ZrAl14Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn4Al43Ni3\\n\",\n        \"output\": \" No, Mn4Al43Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" FeAg\\n\",\n        \"output\": \" No, FeAg does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf11Fe54.9O34.1\\n\",\n        \"output\": \" No, Hf11Fe54.9O34.1 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti11(V2Si)3\\n\",\n        \"output\": \" Yes, Ti11(V2Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CuNi39P10\\n\",\n        \"output\": \" Yes, CuNi39P10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80Si10.5P9.5\\n\",\n        \"output\": \" Yes, Fe80Si10.5P9.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co77.5Si15B7.5\\n\",\n        \"output\": \" Yes, Co77.5Si15B7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4AlNi5\\n\",\n        \"output\": \" Yes, La4AlNi5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al89Fe4Ni7\\n\",\n        \"output\": \" No, Al89Fe4Ni7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2Al3Cu20\\n\",\n        \"output\": \" Yes, Nd2Al3Cu20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg11(Al8Pd5)3\\n\",\n        \"output\": \" No, Mg11(Al8Pd5)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti45Al36Ni19\\n\",\n        \"output\": \" Yes, Ti45Al36Ni19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" vibraphone\\n\",\n        \"output\": \" vibraphone is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn33.6Co50.4B16\\n\",\n        \"output\": \" Yes, Mn33.6Co50.4B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" dugout\\n\",\n        \"output\": \" dugout is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al33Mo17\\n\",\n        \"output\": \" Yes, Al33Mo17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Pd73.5Au10\\n\",\n        \"output\": \" Yes, Si16.5Pd73.5Au10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al10Si7\\n\",\n        \"output\": \" Yes, Mn3Al10Si7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni8P5Pd12\\n\",\n        \"output\": \" Yes, Ni8P5Pd12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr(FeCo2)3\\n\",\n        \"output\": \" Yes, Zr(FeCo2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti4Co16B5\\n\",\n        \"output\": \" Yes, Ti4Co16B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y2(Mg5Ni)3\\n\",\n        \"output\": \" Yes, Y2(Mg5Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe61B39\\n\",\n        \"output\": \" Yes, Fe61B39 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37B3Mo10\\n\",\n        \"output\": \" No, Fe37B3Mo10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La16Al67Ni17\\n\",\n        \"output\": \" Yes, La16Al67Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn(Al2Ge)3\\n\",\n        \"output\": \" Yes, Mn(Al2Ge)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce8Al87Cu5\\n\",\n        \"output\": \" Yes, Ce8Al87Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti5Cu3Ni2\\n\",\n        \"output\": \" Yes, Ti5Cu3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co72.5Si7.5B20\\n\",\n        \"output\": \" Yes, Co72.5Si7.5B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni34B13C3\\n\",\n        \"output\": \" Yes, Ni34B13C3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al49Ni\\n\",\n        \"output\": \" No, Al49Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co83B17\\n\",\n        \"output\": \" Yes, Co83B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Co35B13\\n\",\n        \"output\": \" Yes, Al2Co35B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" forecast\\n\",\n        \"output\": \" forecast is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg3Al17\\n\",\n        \"output\": \" No, Mg3Al17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co41Si4B5\\n\",\n        \"output\": \" No, Co41Si4B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" number\\n\",\n        \"output\": \" number is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co\\n\",\n        \"output\": \" No, Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg7Al2Zn\\n\",\n        \"output\": \" No, Mg7Al2Zn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce8Al87Co5\\n\",\n        \"output\": \" Yes, Ce8Al87Co5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6CuNi3\\n\",\n        \"output\": \" Yes, Zr6CuNi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Co91B2\\n\",\n        \"output\": \" Yes, Zr7Co91B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al42FeNi7\\n\",\n        \"output\": \" No, Al42FeNi7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9.2Cr9.6Co81.2\\n\",\n        \"output\": \" Yes, Zr9.2Cr9.6Co81.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al67.5Si17.5Ni15\\n\",\n        \"output\": \" Yes, Al67.5Si17.5Ni15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdAl43Ni6\\n\",\n        \"output\": \" Yes, NdAl43Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5MgNi4\\n\",\n        \"output\": \" Yes, Nd5MgNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr67Fe6.6Ni26.4\\n\",\n        \"output\": \" Yes, Zr67Fe6.6Ni26.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Mg35Ni6\\n\",\n        \"output\": \" Yes, La9Mg35Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Cu47Ag50\\n\",\n        \"output\": \" Yes, Ce3Cu47Ag50 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe14B5\\n\",\n        \"output\": \" Yes, ZrFe14B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2Al17Ni6\\n\",\n        \"output\": \" Yes, Zr2Al17Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiAl2Cu7\\n\",\n        \"output\": \" No, TiAl2Cu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrVNi2\\n\",\n        \"output\": \" Yes, ZrVNi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Cu42Ag5\\n\",\n        \"output\": \" Yes, Ce3Cu42Ag5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr23Nb20Cu57\\n\",\n        \"output\": \" Yes, Zr23Nb20Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co4B\\n\",\n        \"output\": \" Yes, Co4B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Cu8Ni3\\n\",\n        \"output\": \" Yes, Zr9Cu8Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si4BPd20\\n\",\n        \"output\": \" Yes, Si4BPd20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr53.6Cr20Ni26.4\\n\",\n        \"output\": \" Yes, Zr53.6Cr20Ni26.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni14P5Pt6\\n\",\n        \"output\": \" Yes, Ni14P5Pt6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni19(MoC)3\\n\",\n        \"output\": \" No, Ni19(MoC)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" HfCu5Ni4\\n\",\n        \"output\": \" No, HfCu5Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr11Fe34B5\\n\",\n        \"output\": \" No, Cr11Fe34B5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4Be\\n\",\n        \"output\": \" No, Zr4Be does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ho(Fe5B)4\\n\",\n        \"output\": \" Yes, Ho(Fe5B)4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La11Al5Ni4\\n\",\n        \"output\": \" Yes, La11Al5Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CuNi38P11\\n\",\n        \"output\": \" Yes, CuNi38P11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al10Ni27B13\\n\",\n        \"output\": \" Yes, Al10Ni27B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdAl48Ni\\n\",\n        \"output\": \" No, NdAl48Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39B2Mo9\\n\",\n        \"output\": \" No, Fe39B2Mo9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf76(Nb3Si5)3\\n\",\n        \"output\": \" Yes, Hf76(Nb3Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr12Co9C4\\n\",\n        \"output\": \" Yes, Cr12Co9C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al4Ni33B13\\n\",\n        \"output\": \" Yes, Al4Ni33B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeMg17Ni2\\n\",\n        \"output\": \" Yes, CeMg17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe74.5Si10.5B15\\n\",\n        \"output\": \" Yes, Fe74.5Si10.5B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La15Al2Ni3\\n\",\n        \"output\": \" Yes, La15Al2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni37.5P25Pd37.5\\n\",\n        \"output\": \" Yes, Ni37.5P25Pd37.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn7Al85Ni8\\n\",\n        \"output\": \" No, Mn7Al85Ni8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" SmAl7Ni2\\n\",\n        \"output\": \" Yes, SmAl7Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La30Al53Ni17\\n\",\n        \"output\": \" Yes, La30Al53Ni17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y7Al43\\n\",\n        \"output\": \" Yes, Y7Al43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti13Be6Si\\n\",\n        \"output\": \" Yes, Ti13Be6Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe40B9\\n\",\n        \"output\": \" Yes, ZrFe40B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Ti4Cu11\\n\",\n        \"output\": \" Yes, Zr5Ti4Cu11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8.5V2Co89.5\\n\",\n        \"output\": \" Yes, Zr8.5V2Co89.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" afterthought\\n\",\n        \"output\": \" afterthought is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La5(Mg3Ni2)3\\n\",\n        \"output\": \" Yes, La5(Mg3Ni2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6Co41B3\\n\",\n        \"output\": \" No, Al6Co41B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn7(Ge6Pd25)3\\n\",\n        \"output\": \" Yes, Mn7(Ge6Pd25)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti2P19Pd79\\n\",\n        \"output\": \" Yes, Ti2P19Pd79 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn3Fe37B10\\n\",\n        \"output\": \" Yes, Mn3Fe37B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr36.6Nb15Cu48.4\\n\",\n        \"output\": \" Yes, Zr36.6Nb15Cu48.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd7.3Al85.4Fe7.3\\n\",\n        \"output\": \" Yes, Gd7.3Al85.4Fe7.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Pr3Zr5Fe42\\n\",\n        \"output\": \" Yes, Pr3Zr5Fe42 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe80B13P7\\n\",\n        \"output\": \" Yes, Fe80B13P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" bridge\\n\",\n        \"output\": \" bridge is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni81.5B2P16.5\\n\",\n        \"output\": \" Yes, Ni81.5B2P16.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10V0.036Fe89.964\\n\",\n        \"output\": \" Yes, Zr10V0.036Fe89.964 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu5.9Si18.5Pd75.6\\n\",\n        \"output\": \" Yes, Cu5.9Si18.5Pd75.6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr4(Fe27B5)3\\n\",\n        \"output\": \" Yes, Cr4(Fe27B5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr2Ni2P\\n\",\n        \"output\": \" Yes, Cr2Ni2P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf42Nb43Si15\\n\",\n        \"output\": \" Yes, Hf42Nb43Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si2.5Ni77.5B20\\n\",\n        \"output\": \" No, Si2.5Ni77.5B20 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr7(Ge6Pd25)3\\n\",\n        \"output\": \" Yes, Cr7(Ge6Pd25)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co18W3C4\\n\",\n        \"output\": \" Yes, Co18W3C4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" reindeer\\n\",\n        \"output\": \" reindeer is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Fe91B6\\n\",\n        \"output\": \" No, Mn3Fe91B6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe31W8C11\\n\",\n        \"output\": \" No, Fe31W8C11 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd14Fe78.2B7.8\\n\",\n        \"output\": \" Yes, Nd14Fe78.2B7.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Si\\n\",\n        \"output\": \" No, Ti3Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti13Be5Si2\\n\",\n        \"output\": \" No, Ti13Be5Si2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La5Al44Ni\\n\",\n        \"output\": \" Yes, La5Al44Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti0.8Fe83.2B16\\n\",\n        \"output\": \" Yes, Ti0.8Fe83.2B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg72Zn25\\n\",\n        \"output\": \" Yes, La3Mg72Zn25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr10Fe39B\\n\",\n        \"output\": \" No, Cr10Fe39B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiNi3\\n\",\n        \"output\": \" No, TiNi3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mo8P5Ru12\\n\",\n        \"output\": \" Yes, Mo8P5Ru12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl8Cu\\n\",\n        \"output\": \" Yes, CeAl8Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe85P7.5C7.5\\n\",\n        \"output\": \" No, Fe85P7.5C7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Mg3Cu4\\n\",\n        \"output\": \" Yes, Nd3Mg3Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeCu2Ag7\\n\",\n        \"output\": \" No, CeCu2Ag7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr67.5Be32.5\\n\",\n        \"output\": \" Yes, Zr67.5Be32.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al12Ni31B7\\n\",\n        \"output\": \" No, Al12Ni31B7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe81B6P13\\n\",\n        \"output\": \" Yes, Fe81B6P13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V5Fe37B8\\n\",\n        \"output\": \" Yes, V5Fe37B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2Al17Ni\\n\",\n        \"output\": \" Yes, Nd2Al17Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10Ti4Cu11\\n\",\n        \"output\": \" Yes, Zr10Ti4Cu11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn59.5Co24.5B16\\n\",\n        \"output\": \" Yes, Mn59.5Co24.5B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La6Mg11Cu3\\n\",\n        \"output\": \" No, La6Mg11Cu3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf3Cu7\\n\",\n        \"output\": \" Yes, Hf3Cu7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La8Al11Ni\\n\",\n        \"output\": \" Yes, La8Al11Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ta6Ni13P\\n\",\n        \"output\": \" Yes, Ta6Ni13P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn5Co17B3\\n\",\n        \"output\": \" Yes, Mn5Co17B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Tb33.3Fe66.7\\n\",\n        \"output\": \" No, Tb33.3Fe66.7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CaMg9\\n\",\n        \"output\": \" No, CaMg9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr3(Fe10B)2\\n\",\n        \"output\": \" No, Cr3(Fe10B)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAl89Fe10\\n\",\n        \"output\": \" No, CeAl89Fe10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Mn44Co\\n\",\n        \"output\": \" Yes, Zr5Mn44Co has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Al3Cu5\\n\",\n        \"output\": \" Yes, Ti2Al3Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" TiFe15B4\\n\",\n        \"output\": \" Yes, TiFe15B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr17Cr14Co69\\n\",\n        \"output\": \" Yes, Zr17Cr14Co69 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Pd81.8Au1.7\\n\",\n        \"output\": \" Yes, Si16.5Pd81.8Au1.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni25B19C6\\n\",\n        \"output\": \" Yes, Ni25B19C6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La12Al7Ni\\n\",\n        \"output\": \" Yes, La12Al7Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al15CrSi4\\n\",\n        \"output\": \" No, Al15CrSi4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Al6Cu41\\n\",\n        \"output\": \" No, Nd3Al6Cu41 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr24(NiMo)13\\n\",\n        \"output\": \" Yes, Cr24(NiMo)13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr24.5V25Ni50.5\\n\",\n        \"output\": \" Yes, Zr24.5V25Ni50.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn29Co43B28\\n\",\n        \"output\": \" Yes, Mn29Co43B28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3MgCu6\\n\",\n        \"output\": \" Yes, Nd3MgCu6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca5Mg3Cu2\\n\",\n        \"output\": \" Yes, Ca5Mg3Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn47Co25B28\\n\",\n        \"output\": \" Yes, Mn47Co25B28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al13Cu4\\n\",\n        \"output\": \" No, Mn3Al13Cu4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4Co45Mo\\n\",\n        \"output\": \" Yes, Zr4Co45Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb9.8Fe75.2B15\\n\",\n        \"output\": \" Yes, Nb9.8Fe75.2B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" U20.6Si20.6Pd58.8\\n\",\n        \"output\": \" Yes, U20.6Si20.6Pd58.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al88(CoNi3)3\\n\",\n        \"output\": \" No, Al88(CoNi3)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr41Al7Ni2\\n\",\n        \"output\": \" Yes, Zr41Al7Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Al3Ni10\\n\",\n        \"output\": \" Yes, Zr7Al3Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf3Cu2Ni5\\n\",\n        \"output\": \" Yes, Hf3Cu2Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrNbCo8\\n\",\n        \"output\": \" Yes, ZrNbCo8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2AlCu22\\n\",\n        \"output\": \" No, Ce2AlCu22 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe15B2Mo3\\n\",\n        \"output\": \" Yes, Fe15B2Mo3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf5Cu4Ni\\n\",\n        \"output\": \" Yes, Hf5Cu4Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2Fe17B\\n\",\n        \"output\": \" Yes, Zr2Fe17B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg13Zn7\\n\",\n        \"output\": \" Yes, Mg13Zn7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti15Cu3Ni2\\n\",\n        \"output\": \" No, Ti15Cu3Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" breakfast\\n\",\n        \"output\": \" breakfast is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y6Mg13Cu\\n\",\n        \"output\": \" No, Y6Mg13Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr21Cu28P\\n\",\n        \"output\": \" Yes, Zr21Cu28P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf67(Co8Si3)3\\n\",\n        \"output\": \" Yes, Hf67(Co8Si3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe12Cu3Ag10\\n\",\n        \"output\": \" No, Fe12Cu3Ag10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe5Ni3B2\\n\",\n        \"output\": \" Yes, Fe5Ni3B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr12Fe73B15\\n\",\n        \"output\": \" Yes, Cr12Fe73B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn4Al45Ni\\n\",\n        \"output\": \" No, Mn4Al45Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn29.5Co54.5B16\\n\",\n        \"output\": \" Yes, Mn29.5Co54.5B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co29(Mo4C3)3\\n\",\n        \"output\": \" Yes, Co29(Mo4C3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Mg4Ni3\\n\",\n        \"output\": \" Yes, La3Mg4Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe80B17P3\\n\",\n        \"output\": \" No, Fe80B17P3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr18Ni7\\n\",\n        \"output\": \" Yes, Zr18Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2(Mg5Cu)3\\n\",\n        \"output\": \" Yes, Ce2(Mg5Cu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn(Al7Co)3\\n\",\n        \"output\": \" No, Mn(Al7Co)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7(Fe30B)3\\n\",\n        \"output\": \" Yes, Zr7(Fe30B)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr14La55Cu31\\n\",\n        \"output\": \" Yes, Sr14La55Cu31 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" spot\\n\",\n        \"output\": \" spot is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al6Ni29B15\\n\",\n        \"output\": \" Yes, Al6Ni29B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr3Fe15B2\\n\",\n        \"output\": \" No, Cr3Fe15B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr15Ge3Mo2\\n\",\n        \"output\": \" Yes, Zr15Ge3Mo2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe80B9C11\\n\",\n        \"output\": \" Yes, Fe80B9C11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd50Fe31.5B18.5\\n\",\n        \"output\": \" Yes, Nd50Fe31.5B18.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg20Ti43Al37\\n\",\n        \"output\": \" No, Mg20Ti43Al37 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe76(P5C3)3\\n\",\n        \"output\": \" Yes, Fe76(P5C3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti5Si2Ni3\\n\",\n        \"output\": \" Yes, Ti5Si2Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr6.8V16Co77.2\\n\",\n        \"output\": \" Yes, Zr6.8V16Co77.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg\\n\",\n        \"output\": \" No, Mg does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr46.9Fe30Ni23.1\\n\",\n        \"output\": \" Yes, Zr46.9Fe30Ni23.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39B5Mo6\\n\",\n        \"output\": \" Yes, Fe39B5Mo6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti18CuNi\\n\",\n        \"output\": \" No, Ti18CuNi does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr29Al33Ni38\\n\",\n        \"output\": \" Yes, Zr29Al33Ni38 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La20Al63Ni17\\n\",\n        \"output\": \" Yes, La20Al63Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr6Fe41B3\\n\",\n        \"output\": \" No, Cr6Fe41B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf7Ni3\\n\",\n        \"output\": \" Yes, Hf7Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Co44B\\n\",\n        \"output\": \" Yes, Zr5Co44B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8FeCu11\\n\",\n        \"output\": \" Yes, Zr8FeCu11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr9Ni31P10\\n\",\n        \"output\": \" Yes, Cr9Ni31P10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba10La56.5Cu33.5\\n\",\n        \"output\": \" Yes, Ba10La56.5Cu33.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al47\\n\",\n        \"output\": \" No, Mn3Al47 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb3Fe80B17\\n\",\n        \"output\": \" Yes, Nb3Fe80B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb9.6Fe77.5B12.9\\n\",\n        \"output\": \" Yes, Nb9.6Fe77.5B12.9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr63.65V5Ni31.35\\n\",\n        \"output\": \" Yes, Zr63.65V5Ni31.35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al13Fe3Ni4\\n\",\n        \"output\": \" No, Al13Fe3Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrCu3Ni\\n\",\n        \"output\": \" No, ZrCu3Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr5(Fe4B)4\\n\",\n        \"output\": \" Yes, Cr5(Fe4B)4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr7Fe42B\\n\",\n        \"output\": \" No, Cr7Fe42B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr77.5Cu15B7.5\\n\",\n        \"output\": \" No, Zr77.5Cu15B7.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta12Ni71B17\\n\",\n        \"output\": \" Yes, Ta12Ni71B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" PrZr5Fe44\\n\",\n        \"output\": \" No, PrZr5Fe44 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni7Mo2C\\n\",\n        \"output\": \" Yes, Ni7Mo2C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" TaNi9\\n\",\n        \"output\": \" Yes, TaNi9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3Ni2\\n\",\n        \"output\": \" Yes, Ti3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6Ti5Cu9\\n\",\n        \"output\": \" Yes, Zr6Ti5Cu9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Al7Ni\\n\",\n        \"output\": \" No, Zr2Al7Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Tb30.8Al7.5Fe61.7\\n\",\n        \"output\": \" Yes, Tb30.8Al7.5Fe61.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti8Ni17\\n\",\n        \"output\": \" Yes, Ti8Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe21SiB3\\n\",\n        \"output\": \" Yes, Fe21SiB3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni28B21C\\n\",\n        \"output\": \" Yes, Ni28B21C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti8FeCu11\\n\",\n        \"output\": \" Yes, Ti8FeCu11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CrSi10Pd39\\n\",\n        \"output\": \" Yes, CrSi10Pd39 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2Fe83B15\\n\",\n        \"output\": \" Yes, Zr2Fe83B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10Cr3Ni7\\n\",\n        \"output\": \" Yes, Zr10Cr3Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" HfCu2Ni7\\n\",\n        \"output\": \" No, HfCu2Ni7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr17Al65Ni18\\n\",\n        \"output\": \" Yes, Zr17Al65Ni18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu7Ni33P10\\n\",\n        \"output\": \" No, Cu7Ni33P10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni19(B2C)2\\n\",\n        \"output\": \" Yes, Ni19(B2C)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd5Al4Cu41\\n\",\n        \"output\": \" No, Nd5Al4Cu41 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni77B13C10\\n\",\n        \"output\": \" No, Ni77B13C10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Gd14Co70.6Mo15.4\\n\",\n        \"output\": \" Yes, Gd14Co70.6Mo15.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb5.5Fe81.5B13\\n\",\n        \"output\": \" No, Nb5.5Fe81.5B13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CrCo7P2\\n\",\n        \"output\": \" Yes, CrCo7P2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe16P3C\\n\",\n        \"output\": \" Yes, Fe16P3C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2Co13B5\\n\",\n        \"output\": \" Yes, Zr2Co13B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al88.5Fe3Ni8.5\\n\",\n        \"output\": \" Yes, Al88.5Fe3Ni8.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdCu4\\n\",\n        \"output\": \" No, NdCu4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co13(B3C)3\\n\",\n        \"output\": \" No, Co13(B3C)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe74.5Si18B7.5\\n\",\n        \"output\": \" No, Fe74.5Si18B7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co37Mo5C8\\n\",\n        \"output\": \" No, Co37Mo5C8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnAl44Co5\\n\",\n        \"output\": \" No, MnAl44Co5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr53.6Co20Ni26.4\\n\",\n        \"output\": \" Yes, Zr53.6Co20Ni26.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe91B4Mo5\\n\",\n        \"output\": \" No, Fe91B4Mo5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10.5Co80Mo9.5\\n\",\n        \"output\": \" Yes, Zr10.5Co80Mo9.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39B7Mo4\\n\",\n        \"output\": \" Yes, Fe39B7Mo4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg9Ni8\\n\",\n        \"output\": \" Yes, Nd3Mg9Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni19B29C2\\n\",\n        \"output\": \" No, Ni19B29C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf15V2Si3\\n\",\n        \"output\": \" Yes, Hf15V2Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co16Si3C\\n\",\n        \"output\": \" No, Co16Si3C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe3Ni13P4\\n\",\n        \"output\": \" Yes, Fe3Ni13P4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Pd62.6Au20.9\\n\",\n        \"output\": \" No, Si16.5Pd62.6Au20.9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl8Fe\\n\",\n        \"output\": \" Yes, CeAl8Fe has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" quill\\n\",\n        \"output\": \" quill is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al45Fe4Ni\\n\",\n        \"output\": \" No, Al45Fe4Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5(Fe3Ni2)9\\n\",\n        \"output\": \" Yes, Zr5(Fe3Ni2)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr69Cu30B\\n\",\n        \"output\": \" Yes, Zr69Cu30B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr73Fe10P17\\n\",\n        \"output\": \" Yes, Cr73Fe10P17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe77B20Mo3\\n\",\n        \"output\": \" Yes, Fe77B20Mo3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn2Al43Ni5\\n\",\n        \"output\": \" No, Mn2Al43Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe6B9W85\\n\",\n        \"output\": \" Yes, Fe6B9W85 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnFe19B5\\n\",\n        \"output\": \" Yes, MnFe19B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd3Al17\\n\",\n        \"output\": \" No, Gd3Al17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni12P5Pt3\\n\",\n        \"output\": \" No, Ni12P5Pt3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7CuNi2\\n\",\n        \"output\": \" Yes, Ti7CuNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" trade\\n\",\n        \"output\": \" trade is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe67Mo17C16\\n\",\n        \"output\": \" Yes, Fe67Mo17C16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrTiSi2\\n\",\n        \"output\": \" Yes, ZrTiSi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce8Cu87Ag5\\n\",\n        \"output\": \" No, Ce8Cu87Ag5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr26Fe60.5P13.5\\n\",\n        \"output\": \" Yes, Cr26Fe60.5P13.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe85B8C7\\n\",\n        \"output\": \" Yes, Fe85B8C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Ti22Si75\\n\",\n        \"output\": \" Yes, Zr3Ti22Si75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf51V34Si15\\n\",\n        \"output\": \" Yes, Hf51V34Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Cu6Ni5\\n\",\n        \"output\": \" Yes, Zr9Cu6Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg12AlZn7\\n\",\n        \"output\": \" Yes, Mg12AlZn7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrFe8Co\\n\",\n        \"output\": \" Yes, ZrFe8Co has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr4Cu5Ni\\n\",\n        \"output\": \" Yes, Zr4Cu5Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al83Cu15\\n\",\n        \"output\": \" No, Ce2Al83Cu15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe13Si2C5\\n\",\n        \"output\": \" Yes, Fe13Si2C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79B21\\n\",\n        \"output\": \" Yes, Fe79B21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y10(Al29Ni)3\\n\",\n        \"output\": \" Yes, Y10(Al29Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe93B2Mo5\\n\",\n        \"output\": \" No, Fe93B2Mo5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si15Ni72B13\\n\",\n        \"output\": \" Yes, Si15Ni72B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co37W5C8\\n\",\n        \"output\": \" No, Co37W5C8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce7Al93\\n\",\n        \"output\": \" Yes, Ce7Al93 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Cu2Ni5\\n\",\n        \"output\": \" Yes, Zr3Cu2Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe59B8F33\\n\",\n        \"output\": \" No, Fe59B8F33 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe7Ni9B4\\n\",\n        \"output\": \" Yes, Fe7Ni9B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb8Fe75B17\\n\",\n        \"output\": \" Yes, Nb8Fe75B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe81B10P9\\n\",\n        \"output\": \" Yes, Fe81B10P9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn14.4Co57.6B28\\n\",\n        \"output\": \" Yes, Mn14.4Co57.6B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrFe18B\\n\",\n        \"output\": \" No, ZrFe18B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8VCo41\\n\",\n        \"output\": \" Yes, Zr8VCo41 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CuNi40P9\\n\",\n        \"output\": \" Yes, CuNi40P9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co27Mo14C9\\n\",\n        \"output\": \" Yes, Co27Mo14C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co7SiB2\\n\",\n        \"output\": \" Yes, Co7SiB2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe80P17.5C2.5\\n\",\n        \"output\": \" Yes, Fe80P17.5C2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co35Mo8C7\\n\",\n        \"output\": \" No, Co35Mo8C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe77Si11B12\\n\",\n        \"output\": \" Yes, Fe77Si11B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al8Fe31B11\\n\",\n        \"output\": \" Yes, Al8Fe31B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr17.5Cr4Co78.5\\n\",\n        \"output\": \" Yes, Zr17.5Cr4Co78.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr24Co17C9\\n\",\n        \"output\": \" Yes, Cr24Co17C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni13(B5C)2\\n\",\n        \"output\": \" Yes, Ni13(B5C)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeCu5Ag14\\n\",\n        \"output\": \" No, CeCu5Ag14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al39Fe5Ge6\\n\",\n        \"output\": \" Yes, Al39Fe5Ge6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr3Ni77P20\\n\",\n        \"output\": \" Yes, Cr3Ni77P20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr11Fe29C10\\n\",\n        \"output\": \" No, Cr11Fe29C10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe72.5P17.5C10\\n\",\n        \"output\": \" Yes, Fe72.5P17.5C10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" SiNi4\\n\",\n        \"output\": \" No, SiNi4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Ti3Si14\\n\",\n        \"output\": \" Yes, Zr3Ti3Si14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al45Fe4Si\\n\",\n        \"output\": \" No, Al45Fe4Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CaMg8Zn\\n\",\n        \"output\": \" Yes, CaMg8Zn has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf(CuNi2)3\\n\",\n        \"output\": \" No, Hf(CuNi2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn5Fe89B6\\n\",\n        \"output\": \" No, Mn5Fe89B6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni20B4C\\n\",\n        \"output\": \" Yes, Ni20B4C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr24Fe56.5P19.5\\n\",\n        \"output\": \" Yes, Cr24Fe56.5P19.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ni15Pd68.5\\n\",\n        \"output\": \" Yes, Si16.5Ni15Pd68.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn85(Fe2B3)3\\n\",\n        \"output\": \" Yes, Mn85(Fe2B3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al16Ni\\n\",\n        \"output\": \" No, Ce3Al16Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe44BMo5\\n\",\n        \"output\": \" No, Fe44BMo5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm6Al39Ni5\\n\",\n        \"output\": \" Yes, Sm6Al39Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr37Al12Ni\\n\",\n        \"output\": \" Yes, Zr37Al12Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3Al22\\n\",\n        \"output\": \" Yes, Ce3Al22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrNb3Si\\n\",\n        \"output\": \" Yes, ZrNb3Si has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr32.3Nb25Cu42.7\\n\",\n        \"output\": \" Yes, Zr32.3Nb25Cu42.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf12Nb5Si3\\n\",\n        \"output\": \" Yes, Hf12Nb5Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb40Si9C\\n\",\n        \"output\": \" Yes, Nb40Si9C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La11Al5Cu4\\n\",\n        \"output\": \" Yes, La11Al5Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeMg7Ni2\\n\",\n        \"output\": \" Yes, CeMg7Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77Ni5B18\\n\",\n        \"output\": \" Yes, Fe77Ni5B18 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu3Ni73P24\\n\",\n        \"output\": \" No, Cu3Ni73P24 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Ni78B17\\n\",\n        \"output\": \" Yes, Zr5Ni78B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu20.9Si16.5Pd62.6\\n\",\n        \"output\": \" Yes, Cu20.9Si16.5Pd62.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13(Ti4Si25)3\\n\",\n        \"output\": \" Yes, Zr13(Ti4Si25)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd7MgNi2\\n\",\n        \"output\": \" No, Nd7MgNi2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Tb30.8Fe61.7Si7.5\\n\",\n        \"output\": \" Yes, Tb30.8Fe61.7Si7.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2(Mg5Cu)3\\n\",\n        \"output\": \" No, La2(Mg5Cu)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3AlNi\\n\",\n        \"output\": \" Yes, La3AlNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca7La61Cu32\\n\",\n        \"output\": \" Yes, Ca7La61Cu32 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba2La71Cu27\\n\",\n        \"output\": \" Yes, Ba2La71Cu27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn4Al9Si7\\n\",\n        \"output\": \" Yes, Mn4Al9Si7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeMg13Cu6\\n\",\n        \"output\": \" Yes, CeMg13Cu6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Gd2Al23\\n\",\n        \"output\": \" Yes, Gd2Al23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdAlCu8\\n\",\n        \"output\": \" No, NdAlCu8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16Ag5Pd79\\n\",\n        \"output\": \" Yes, Si16Ag5Pd79 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti22(Al3Ni)7\\n\",\n        \"output\": \" Yes, Ti22(Al3Ni)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al2Cu3\\n\",\n        \"output\": \" No, Al2Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" motorboat\\n\",\n        \"output\": \" motorboat is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg16Cu3\\n\",\n        \"output\": \" Yes, CeMg16Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta5(Ni4P)9\\n\",\n        \"output\": \" Yes, Ta5(Ni4P)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni37.5P25Pt37.5\\n\",\n        \"output\": \" Yes, Ni37.5P25Pt37.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Nb2Si\\n\",\n        \"output\": \" No, Ti7Nb2Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti8Al5Ni7\\n\",\n        \"output\": \" Yes, Ti8Al5Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe(CuAg)2\\n\",\n        \"output\": \" No, Fe(CuAg)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co3MoC\\n\",\n        \"output\": \" Yes, Co3MoC has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Co37W6\\n\",\n        \"output\": \" Yes, Zr7Co37W6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11Cu8B\\n\",\n        \"output\": \" Yes, Zr11Cu8B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Al38Ni9\\n\",\n        \"output\": \" Yes, Zr3Al38Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co15Si4B\\n\",\n        \"output\": \" No, Co15Si4B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb80Si19Ge\\n\",\n        \"output\": \" Yes, Nb80Si19Ge has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe65B22.5F12.5\\n\",\n        \"output\": \" Yes, Fe65B22.5F12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Cu5Ni3\\n\",\n        \"output\": \" Yes, Zr12Cu5Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3Al15Fe2\\n\",\n        \"output\": \" No, Ce3Al15Fe2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2(Al5Ni)3\\n\",\n        \"output\": \" Yes, Ce2(Al5Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr17(Al6Ni5)3\\n\",\n        \"output\": \" Yes, Zr17(Al6Ni5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti6Be3Si\\n\",\n        \"output\": \" No, Ti6Be3Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni30B17C3\\n\",\n        \"output\": \" Yes, Ni30B17C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Cu62Ag35\\n\",\n        \"output\": \" No, Ce3Cu62Ag35 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf7Fe91B2\\n\",\n        \"output\": \" Yes, Hf7Fe91B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15.5V10Co74.5\\n\",\n        \"output\": \" Yes, Zr15.5V10Co74.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf28(Nb5Cu19)3\\n\",\n        \"output\": \" Yes, Hf28(Nb5Cu19)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" chemistry\\n\",\n        \"output\": \" chemistry is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" kiss\\n\",\n        \"output\": \" kiss is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg14AlZn5\\n\",\n        \"output\": \" Yes, Mg14AlZn5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe59Ni25B16\\n\",\n        \"output\": \" Yes, Fe59Ni25B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Be2\\n\",\n        \"output\": \" Yes, Zr3Be2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd16.8Fe67.2B16\\n\",\n        \"output\": \" Yes, Nd16.8Fe67.2B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni19B25C6\\n\",\n        \"output\": \" Yes, Ni19B25C6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sc3Fe\\n\",\n        \"output\": \" Yes, Sc3Fe has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd9Fe41\\n\",\n        \"output\": \" Yes, Nd9Fe41 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr11.2Co82.2W6.6\\n\",\n        \"output\": \" Yes, Zr11.2Co82.2W6.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2Mg37Zn11\\n\",\n        \"output\": \" Yes, La2Mg37Zn11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5Al7Cu38\\n\",\n        \"output\": \" No, Nd5Al7Cu38 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" attempt\\n\",\n        \"output\": \" attempt is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg17Zn3\\n\",\n        \"output\": \" No, Mg17Zn3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al44Fe5Co\\n\",\n        \"output\": \" No, Al44Fe5Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al9Cr\\n\",\n        \"output\": \" No, Al9Cr does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe37Ni37B26\\n\",\n        \"output\": \" Yes, Fe37Ni37B26 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg3Cu\\n\",\n        \"output\": \" Yes, YMg3Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd20.625Fe61.875B17.5\\n\",\n        \"output\": \" Yes, Nd20.625Fe61.875B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb6.9Fe80B13.1\\n\",\n        \"output\": \" Yes, Nb6.9Fe80B13.1 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Al21Ni2\\n\",\n        \"output\": \" Yes, Zr2Al21Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" GdAl17Ni2\\n\",\n        \"output\": \" Yes, GdAl17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YAl9\\n\",\n        \"output\": \" Yes, YAl9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaMg2Ni\\n\",\n        \"output\": \" Yes, LaMg2Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg7AlZn2\\n\",\n        \"output\": \" Yes, Mg7AlZn2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn21Co21B8\\n\",\n        \"output\": \" Yes, Mn21Co21B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co15(B3C2)2\\n\",\n        \"output\": \" Yes, Co15(B3C2)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co15Si4C\\n\",\n        \"output\": \" No, Co15Si4C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti10Nb7Si3\\n\",\n        \"output\": \" Yes, Ti10Nb7Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb15Fe4Co81\\n\",\n        \"output\": \" Yes, Nb15Fe4Co81 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al13V2Ge5\\n\",\n        \"output\": \" Yes, Al13V2Ge5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg33Ti14Al3\\n\",\n        \"output\": \" No, Mg33Ti14Al3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe7CuB2\\n\",\n        \"output\": \" No, Fe7CuB2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si8.5Ni66B25.5\\n\",\n        \"output\": \" Yes, Si8.5Ni66B25.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti30.1Nb30Cu39.9\\n\",\n        \"output\": \" Yes, Ti30.1Nb30Cu39.9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe82B11C7\\n\",\n        \"output\": \" Yes, Fe82B11C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" signature\\n\",\n        \"output\": \" signature is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" calculator\\n\",\n        \"output\": \" calculator is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Cr5Co13\\n\",\n        \"output\": \" Yes, Zr2Cr5Co13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al13Cr4Ge3\\n\",\n        \"output\": \" No, Al13Cr4Ge3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe3Co37B10\\n\",\n        \"output\": \" Yes, Fe3Co37B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83B7P10\\n\",\n        \"output\": \" Yes, Fe83B7P10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr56.95Mn15Ni28.05\\n\",\n        \"output\": \" Yes, Zr56.95Mn15Ni28.05 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn17.6Co70.4B12\\n\",\n        \"output\": \" Yes, Mn17.6Co70.4B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe20WC4\\n\",\n        \"output\": \" No, Fe20WC4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd7Fe13\\n\",\n        \"output\": \" Yes, Nd7Fe13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu7Si17Pd76\\n\",\n        \"output\": \" Yes, Cu7Si17Pd76 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg16Cu3\\n\",\n        \"output\": \" Yes, NdMg16Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Gd3Al14Ni3\\n\",\n        \"output\": \" Yes, Gd3Al14Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca11Mg89\\n\",\n        \"output\": \" No, Ca11Mg89 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf2Cu7Ni\\n\",\n        \"output\": \" No, Hf2Cu7Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si4Ni15C\\n\",\n        \"output\": \" No, Si4Ni15C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl7Cu2\\n\",\n        \"output\": \" No, CeAl7Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti5.9Al94.1\\n\",\n        \"output\": \" No, Ti5.9Al94.1 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si7.5Ni70B22.5\\n\",\n        \"output\": \" Yes, Si7.5Ni70B22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Nb5Si2\\n\",\n        \"output\": \" No, Zr3Nb5Si2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti(CuNi)2\\n\",\n        \"output\": \" No, Ti(CuNi)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb15Fe42.5Co42.5\\n\",\n        \"output\": \" Yes, Nb15Fe42.5Co42.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al13Cr2Si5\\n\",\n        \"output\": \" Yes, Al13Cr2Si5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co3.5Ni77P19.5\\n\",\n        \"output\": \" Yes, Co3.5Ni77P19.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Ag1.7Pd81.8\\n\",\n        \"output\": \" Yes, Si16.5Ag1.7Pd81.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al11V2Cu7\\n\",\n        \"output\": \" Yes, Al11V2Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb19(Si2Ge)2\\n\",\n        \"output\": \" Yes, Nb19(Si2Ge)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2MgNi2\\n\",\n        \"output\": \" Yes, Y2MgNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn35Co37B28\\n\",\n        \"output\": \" Yes, Mn35Co37B28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8(Cr3Co11)3\\n\",\n        \"output\": \" Yes, Zr8(Cr3Co11)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti11Al2Cu7\\n\",\n        \"output\": \" Yes, Ti11Al2Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Co17Si\\n\",\n        \"output\": \" Yes, Zr2Co17Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti10V7Si3\\n\",\n        \"output\": \" No, Ti10V7Si3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe76Mo7P17\\n\",\n        \"output\": \" Yes, Fe76Mo7P17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3GePd21\\n\",\n        \"output\": \" Yes, Si3GePd21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrAl5Ni4\\n\",\n        \"output\": \" No, ZrAl5Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd9Al85Ni6\\n\",\n        \"output\": \" Yes, Nd9Al85Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr3Si20Pd77\\n\",\n        \"output\": \" Yes, Cr3Si20Pd77 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Nb13Si4\\n\",\n        \"output\": \" Yes, Zr3Nb13Si4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr54.4Al15Ni30.6\\n\",\n        \"output\": \" Yes, Zr54.4Al15Ni30.6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd6Mg3Ni\\n\",\n        \"output\": \" No, Nd6Mg3Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al43Co4\\n\",\n        \"output\": \" No, Mn3Al43Co4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe17(Cu5Ag6)3\\n\",\n        \"output\": \" No, Fe17(Cu5Ag6)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Mg17\\n\",\n        \"output\": \" Yes, Y3Mg17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" tyvek\\n\",\n        \"output\": \" tyvek is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnAl14Si5\\n\",\n        \"output\": \" No, MnAl14Si5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13Cu5B2\\n\",\n        \"output\": \" Yes, Zr13Cu5B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Al5Cu2\\n\",\n        \"output\": \" No, La3Al5Cu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si18Ni32.8Pd49.2\\n\",\n        \"output\": \" Yes, Si18Ni32.8Pd49.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiAl4Ni5\\n\",\n        \"output\": \" No, TiAl4Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Al5Ni6\\n\",\n        \"output\": \" Yes, La9Al5Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al4Cu\\n\",\n        \"output\": \" No, Al4Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sb22.5Pb22.5Au55\\n\",\n        \"output\": \" Yes, Sb22.5Pb22.5Au55 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni19C\\n\",\n        \"output\": \" No, Ni19C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf10Nb7Si3\\n\",\n        \"output\": \" Yes, Hf10Nb7Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti37Al52Ni11\\n\",\n        \"output\": \" Yes, Ti37Al52Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu4.5Si18Pd77.5\\n\",\n        \"output\": \" Yes, Cu4.5Si18Pd77.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg27Ti45Al28\\n\",\n        \"output\": \" Yes, Mg27Ti45Al28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co77.5W10C12.5\\n\",\n        \"output\": \" No, Co77.5W10C12.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al89Fe2Ni9\\n\",\n        \"output\": \" No, Al89Fe2Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti2CuNi7\\n\",\n        \"output\": \" No, Ti2CuNi7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr65Al7.5Cu27.5\\n\",\n        \"output\": \" Yes, Zr65Al7.5Cu27.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La(MgCu)2\\n\",\n        \"output\": \" Yes, La(MgCu)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeCu15Ag4\\n\",\n        \"output\": \" No, CeCu15Ag4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn2(Al15Co)3\\n\",\n        \"output\": \" No, Mn2(Al15Co)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnFe39B10\\n\",\n        \"output\": \" Yes, MnFe39B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al13V3Ge4\\n\",\n        \"output\": \" No, Al13V3Ge4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb7Si2Mo\\n\",\n        \"output\": \" Yes, Nb7Si2Mo has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr22Ti13Si15\\n\",\n        \"output\": \" Yes, Zr22Ti13Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr5Ni11B4\\n\",\n        \"output\": \" Yes, Cr5Ni11B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" maria\\n\",\n        \"output\": \" maria is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni33Mo10C7\\n\",\n        \"output\": \" Yes, Ni33Mo10C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr72.5Ni13.5P14\\n\",\n        \"output\": \" No, Cr72.5Ni13.5P14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79Co4B17\\n\",\n        \"output\": \" Yes, Fe79Co4B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al87Co4Ni9\\n\",\n        \"output\": \" No, Al87Co4Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Mg13Cu4\\n\",\n        \"output\": \" Yes, Ce3Mg13Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Al20Ni21\\n\",\n        \"output\": \" Yes, La9Al20Ni21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2Al83Ni15\\n\",\n        \"output\": \" No, Zr2Al83Ni15 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2Mg11Cu7\\n\",\n        \"output\": \" Yes, Nd2Mg11Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V3Fe15B2\\n\",\n        \"output\": \" No, V3Fe15B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaAl41Ni8\\n\",\n        \"output\": \" Yes, LaAl41Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2Mg7Ag\\n\",\n        \"output\": \" Yes, Y2Mg7Ag has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Mg17Cu\\n\",\n        \"output\": \" No, Ce2Mg17Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe12.5Si6B81.5\\n\",\n        \"output\": \" No, Fe12.5Si6B81.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" V5(Fe13B2)3\\n\",\n        \"output\": \" Yes, V5(Fe13B2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb5.5Fe85.5B9\\n\",\n        \"output\": \" No, Nb5.5Fe85.5B9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al26Cr5Si19\\n\",\n        \"output\": \" Yes, Al26Cr5Si19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2(Fe5B)3\\n\",\n        \"output\": \" Yes, Zr2(Fe5B)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ta10Ni31P9\\n\",\n        \"output\": \" Yes, Ta10Ni31P9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn27Co61B12\\n\",\n        \"output\": \" Yes, Mn27Co61B12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd33.3Al33.4Fe33.3\\n\",\n        \"output\": \" Yes, Gd33.3Al33.4Fe33.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr53.6Fe20Ni26.4\\n\",\n        \"output\": \" Yes, Zr53.6Fe20Ni26.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti9Si2Ni9\\n\",\n        \"output\": \" No, Ti9Si2Ni9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd4Al43Ni3\\n\",\n        \"output\": \" Yes, Nd4Al43Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrCo7B2\\n\",\n        \"output\": \" Yes, ZrCo7B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe67Cu10Ag23\\n\",\n        \"output\": \" No, Fe67Cu10Ag23 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe83Ni3B14\\n\",\n        \"output\": \" Yes, Fe83Ni3B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al7Ni18\\n\",\n        \"output\": \" No, Al7Ni18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni38.5P23Pd38.5\\n\",\n        \"output\": \" Yes, Ni38.5P23Pd38.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe35W4C11\\n\",\n        \"output\": \" No, Fe35W4C11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe19WC5\\n\",\n        \"output\": \" No, Fe19WC5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11Ti22Cu17\\n\",\n        \"output\": \" No, Zr11Ti22Cu17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5.2Co84.8W10\\n\",\n        \"output\": \" Yes, Zr5.2Co84.8W10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr38Al11Ni\\n\",\n        \"output\": \" Yes, Zr38Al11Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al22Fe2Ni\\n\",\n        \"output\": \" No, Al22Fe2Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti17Si2Ni\\n\",\n        \"output\": \" No, Ti17Si2Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn18Al57Ge25\\n\",\n        \"output\": \" Yes, Mn18Al57Ge25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd(Mg2Cu)3\\n\",\n        \"output\": \" Yes, Nd(Mg2Cu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe70Si7.5B22.5\\n\",\n        \"output\": \" Yes, Fe70Si7.5B22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Sm2Al7Ni\\n\",\n        \"output\": \" Yes, Sm2Al7Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb7Fe83B10\\n\",\n        \"output\": \" Yes, Nb7Fe83B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg5AlZn4\\n\",\n        \"output\": \" No, Mg5AlZn4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce8Al87Fe5\\n\",\n        \"output\": \" Yes, Ce8Al87Fe5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf64(V7Si5)3\\n\",\n        \"output\": \" Yes, Hf64(V7Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn14FeB5\\n\",\n        \"output\": \" Yes, Mn14FeB5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La5(Al2Ni3)3\\n\",\n        \"output\": \" Yes, La5(Al2Ni3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu26.7Si16.5Pd56.8\\n\",\n        \"output\": \" No, Cu26.7Si16.5Pd56.8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr60.3Cu10Ni29.7\\n\",\n        \"output\": \" Yes, Zr60.3Cu10Ni29.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe2Co7\\n\",\n        \"output\": \" Yes, ZrFe2Co7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al4Ni37B9\\n\",\n        \"output\": \" Yes, Al4Ni37B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe31.5Ni50.5B18\\n\",\n        \"output\": \" Yes, Fe31.5Ni50.5B18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti23Al67Ni10\\n\",\n        \"output\": \" Yes, Ti23Al67Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3Ni80B17\\n\",\n        \"output\": \" Yes, Si3Ni80B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Co89Mo4\\n\",\n        \"output\": \" Yes, Zr7Co89Mo4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg51Ti40Al9\\n\",\n        \"output\": \" No, Mg51Ti40Al9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe20Cu11Ag19\\n\",\n        \"output\": \" Yes, Fe20Cu11Ag19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si3Ni70B27\\n\",\n        \"output\": \" Yes, Si3Ni70B27 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al23FeNi\\n\",\n        \"output\": \" No, Al23FeNi does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al12VCu7\\n\",\n        \"output\": \" No, Al12VCu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si17B12Mo71\\n\",\n        \"output\": \" Yes, Si17B12Mo71 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe37B10Mo3\\n\",\n        \"output\": \" Yes, Fe37B10Mo3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al17Fe\\n\",\n        \"output\": \" Yes, Ce2Al17Fe has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2Al43Ni5\\n\",\n        \"output\": \" Yes, Nd2Al43Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sm9Al85Ni6\\n\",\n        \"output\": \" Yes, Sm9Al85Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Mg7Ni\\n\",\n        \"output\": \" Yes, Nd2Mg7Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe80.5B17W2.5\\n\",\n        \"output\": \" Yes, Fe80.5B17W2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4Fe39B7\\n\",\n        \"output\": \" Yes, Zr4Fe39B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd11Al5Ni4\\n\",\n        \"output\": \" Yes, Gd11Al5Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni29(B5C2)3\\n\",\n        \"output\": \" Yes, Ni29(B5C2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Al2Ni\\n\",\n        \"output\": \" Yes, Zr7Al2Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf69Nb16Si15\\n\",\n        \"output\": \" Yes, Hf69Nb16Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe87CuB12\\n\",\n        \"output\": \" No, Fe87CuB12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti6AlNi3\\n\",\n        \"output\": \" Yes, Ti6AlNi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr8V5Ni12\\n\",\n        \"output\": \" Yes, Zr8V5Ni12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co14(WC)3\\n\",\n        \"output\": \" Yes, Co14(WC)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti12Al3Ni5\\n\",\n        \"output\": \" Yes, Ti12Al3Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" panther\\n\",\n        \"output\": \" panther is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe77B10F13\\n\",\n        \"output\": \" Yes, Fe77B10F13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti11Be9\\n\",\n        \"output\": \" No, Ti11Be9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2Al5Ni3\\n\",\n        \"output\": \" Yes, La2Al5Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe50Co33B17\\n\",\n        \"output\": \" Yes, Fe50Co33B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti(CuNi2)3\\n\",\n        \"output\": \" No, Ti(CuNi2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5(Al13Ni2)3\\n\",\n        \"output\": \" Yes, Zr5(Al13Ni2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca2Al17Fe\\n\",\n        \"output\": \" Yes, Ca2Al17Fe has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al44(FeCo)3\\n\",\n        \"output\": \" No, Al44(FeCo)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CuNi7P2\\n\",\n        \"output\": \" Yes, CuNi7P2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Sr6La29Cu15\\n\",\n        \"output\": \" Yes, Sr6La29Cu15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr37Ni12P\\n\",\n        \"output\": \" Yes, Zr37Ni12P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca1La71.5Cu27.5\\n\",\n        \"output\": \" Yes, Ca1La71.5Cu27.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb19Si5Ge\\n\",\n        \"output\": \" Yes, Nb19Si5Ge has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnAl45Ni4\\n\",\n        \"output\": \" No, MnAl45Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5Mg88Ni7\\n\",\n        \"output\": \" Yes, Nd5Mg88Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al23Ni2\\n\",\n        \"output\": \" No, Al23Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf14(VSi)3\\n\",\n        \"output\": \" Yes, Hf14(VSi)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd14Si11\\n\",\n        \"output\": \" Yes, Gd14Si11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Fe93B4\\n\",\n        \"output\": \" No, Zr3Fe93B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al44(FeNi)3\\n\",\n        \"output\": \" No, Al44(FeNi)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr63Nb30Si7\\n\",\n        \"output\": \" No, Zr63Nb30Si7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe17Cu5B3\\n\",\n        \"output\": \" No, Fe17Cu5B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr85Al8Si7\\n\",\n        \"output\": \" Yes, Zr85Al8Si7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Fe5B3\\n\",\n        \"output\": \" Yes, Al2Fe5B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co16W3C\\n\",\n        \"output\": \" No, Co16W3C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr9Fe35B6\\n\",\n        \"output\": \" Yes, Cr9Fe35B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8AlNi11\\n\",\n        \"output\": \" Yes, Zr8AlNi11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe36Si5B9\\n\",\n        \"output\": \" Yes, Fe36Si5B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni23B23C4\\n\",\n        \"output\": \" No, Ni23B23C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn21Co15B14\\n\",\n        \"output\": \" Yes, Mn21Co15B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr62.5Cu30B7.5\\n\",\n        \"output\": \" Yes, Zr62.5Cu30B7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NbFe17B2\\n\",\n        \"output\": \" Yes, NbFe17B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al86Co3Ni11\\n\",\n        \"output\": \" No, Al86Co3Ni11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe42B3Mo5\\n\",\n        \"output\": \" No, Fe42B3Mo5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5(Fe4Co)9\\n\",\n        \"output\": \" Yes, Zr5(Fe4Co)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CrSi4Pd15\\n\",\n        \"output\": \" Yes, CrSi4Pd15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.9Cu33Ni0.1\\n\",\n        \"output\": \" Yes, Zr66.9Cu33Ni0.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Si4Ni3\\n\",\n        \"output\": \" No, Ti3Si4Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al88(FeNi3)3\\n\",\n        \"output\": \" Yes, Al88(FeNi3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe66.4Ni16.6B17\\n\",\n        \"output\": \" Yes, Fe66.4Ni16.6B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni16(Mo2C)3\\n\",\n        \"output\": \" Yes, Ni16(Mo2C)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al89Fe9Ni2\\n\",\n        \"output\": \" No, Al89Fe9Ni2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf67(Nb6Si5)3\\n\",\n        \"output\": \" Yes, Hf67(Nb6Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Al73Ni20\\n\",\n        \"output\": \" Yes, Zr7Al73Ni20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NbNi\\n\",\n        \"output\": \" Yes, NbNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3Cu57Ag40\\n\",\n        \"output\": \" Yes, Ce3Cu57Ag40 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr9(Co3C)4\\n\",\n        \"output\": \" No, Cr9(Co3C)4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd5Mg13Ni2\\n\",\n        \"output\": \" Yes, Nd5Mg13Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr9Co11C5\\n\",\n        \"output\": \" Yes, Cr9Co11C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr67(Co2P)11\\n\",\n        \"output\": \" Yes, Zr67(Co2P)11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La5AlNi4\\n\",\n        \"output\": \" Yes, La5AlNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al4Fe37B9\\n\",\n        \"output\": \" Yes, Al4Fe37B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe39B11\\n\",\n        \"output\": \" Yes, Fe39B11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al47Ni3\\n\",\n        \"output\": \" No, Al47Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Al7Cu40\\n\",\n        \"output\": \" No, Ce3Al7Cu40 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Fe78B19\\n\",\n        \"output\": \" Yes, Zr3Fe78B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11(AlNi2)3\\n\",\n        \"output\": \" Yes, Zr11(AlNi2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm3Al47\\n\",\n        \"output\": \" No, Sm3Al47 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn26.4Co61.6B12\\n\",\n        \"output\": \" Yes, Mn26.4Co61.6B12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb77Si23\\n\",\n        \"output\": \" Yes, Nb77Si23 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe33W10C7\\n\",\n        \"output\": \" No, Fe33W10C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79B10F11\\n\",\n        \"output\": \" Yes, Fe79B10F11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn4Al45Co\\n\",\n        \"output\": \" No, Mn4Al45Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" consonant\\n\",\n        \"output\": \" consonant is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr21Nb22Cu57\\n\",\n        \"output\": \" Yes, Zr21Nb22Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn51.5Co28.5B20\\n\",\n        \"output\": \" Yes, Mn51.5Co28.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe4Ni16P5\\n\",\n        \"output\": \" Yes, Fe4Ni16P5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti6Cu3Ni\\n\",\n        \"output\": \" Yes, Ti6Cu3Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" FeNi14B5\\n\",\n        \"output\": \" Yes, FeNi14B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Al88Ni9\\n\",\n        \"output\": \" Yes, Y3Al88Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaMg7Cu2\\n\",\n        \"output\": \" Yes, LaMg7Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti18Ni7\\n\",\n        \"output\": \" Yes, Ti18Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg5Al4Zn\\n\",\n        \"output\": \" No, Mg5Al4Zn does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe84Si3B13\\n\",\n        \"output\": \" Yes, Fe84Si3B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" mountain\\n\",\n        \"output\": \" mountain is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAl46Ni3\\n\",\n        \"output\": \" No, MnAl46Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3(Al10Cu)2\\n\",\n        \"output\": \" Yes, Y3(Al10Cu)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ga4Fe79B17\\n\",\n        \"output\": \" Yes, Ga4Fe79B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83CuB16\\n\",\n        \"output\": \" No, Fe83CuB16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca70Mg7.5Al22.5\\n\",\n        \"output\": \" Yes, Ca70Mg7.5Al22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11(CuNi2)3\\n\",\n        \"output\": \" Yes, Zr11(CuNi2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd3Au\\n\",\n        \"output\": \" Yes, Gd3Au has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La7.5Zr7.5Al85\\n\",\n        \"output\": \" Yes, La7.5Zr7.5Al85 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2VCo17\\n\",\n        \"output\": \" Yes, Zr2VCo17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu82.8Ag9P8.2\\n\",\n        \"output\": \" Yes, Cu82.8Ag9P8.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Pd77.5Au6\\n\",\n        \"output\": \" Yes, Si16.5Pd77.5Au6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd9Fe82B9\\n\",\n        \"output\": \" Yes, Nd9Fe82B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe69Cu15B16\\n\",\n        \"output\": \" No, Fe69Cu15B16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti15Al19Ni16\\n\",\n        \"output\": \" Yes, Ti15Al19Ni16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Si3Ni4\\n\",\n        \"output\": \" No, Ti3Si3Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnAl12Si7\\n\",\n        \"output\": \" No, MnAl12Si7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti4Cu5Ni\\n\",\n        \"output\": \" Yes, Ti4Cu5Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni67B17C16\\n\",\n        \"output\": \" No, Ni67B17C16 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La13Al6Ni\\n\",\n        \"output\": \" Yes, La13Al6Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8Fe75B17\\n\",\n        \"output\": \" Yes, Zr8Fe75B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si9Pd39Au2\\n\",\n        \"output\": \" Yes, Si9Pd39Au2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni22.5P25Pt52.5\\n\",\n        \"output\": \" Yes, Ni22.5P25Pt52.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni16P5Pd4\\n\",\n        \"output\": \" Yes, Ni16P5Pd4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Fe87\\n\",\n        \"output\": \" No, Zr13Fe87 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4Co17B4\\n\",\n        \"output\": \" Yes, Zr4Co17B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" fly\\n\",\n        \"output\": \" fly is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg15AlZn4\\n\",\n        \"output\": \" Yes, Mg15AlZn4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca7.5La56.5Cu36\\n\",\n        \"output\": \" Yes, Ca7.5La56.5Cu36 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr66.95Mn33Ni0.05\\n\",\n        \"output\": \" Yes, Zr66.95Mn33Ni0.05 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiCo19B5\\n\",\n        \"output\": \" Yes, TiCo19B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80P7.5C12.5\\n\",\n        \"output\": \" Yes, Fe80P7.5C12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe40BMo9\\n\",\n        \"output\": \" No, Fe40BMo9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe31W10C9\\n\",\n        \"output\": \" No, Fe31W10C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg27Ti52Al21\\n\",\n        \"output\": \" No, Mg27Ti52Al21 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3Ni19B3\\n\",\n        \"output\": \" Yes, Si3Ni19B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr17.5Cr8Co74.5\\n\",\n        \"output\": \" Yes, Zr17.5Cr8Co74.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr87Ge13\\n\",\n        \"output\": \" Yes, Zr87Ge13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Al3Ni2\\n\",\n        \"output\": \" Yes, Zr5Al3Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sm10Al89Ni\\n\",\n        \"output\": \" Yes, Sm10Al89Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al85Fe2Ni13\\n\",\n        \"output\": \" No, Al85Fe2Ni13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al23Co2\\n\",\n        \"output\": \" No, Al23Co2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al15Cr3Si2\\n\",\n        \"output\": \" No, Al15Cr3Si2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe16SiB3\\n\",\n        \"output\": \" Yes, Fe16SiB3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CaMg17Cu2\\n\",\n        \"output\": \" No, CaMg17Cu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba5La29Cu16\\n\",\n        \"output\": \" Yes, Ba5La29Cu16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr23Al17Ni10\\n\",\n        \"output\": \" Yes, Zr23Al17Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" cover\\n\",\n        \"output\": \" cover is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe7NiB2\\n\",\n        \"output\": \" Yes, Fe7NiB2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce5NbAl44\\n\",\n        \"output\": \" Yes, Ce5NbAl44 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si8B17Mo75\\n\",\n        \"output\": \" Yes, Si8B17Mo75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co77.5W7.5C15\\n\",\n        \"output\": \" No, Co77.5W7.5C15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn13(CoB)6\\n\",\n        \"output\": \" Yes, Mn13(CoB)6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe83B14P3\\n\",\n        \"output\": \" Yes, Fe83B14P3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr12Al8Ni5\\n\",\n        \"output\": \" Yes, Zr12Al8Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Al5Ni2\\n\",\n        \"output\": \" No, Zr3Al5Ni2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf63Nb22Si15\\n\",\n        \"output\": \" Yes, Hf63Nb22Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu81.5Ag12.2P6.3\\n\",\n        \"output\": \" No, Cu81.5Ag12.2P6.3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al17Co2Ni\\n\",\n        \"output\": \" No, Al17Co2Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe3Cu7\\n\",\n        \"output\": \" No, Fe3Cu7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La(AlNi2)3\\n\",\n        \"output\": \" No, La(AlNi2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeCu7Ag2\\n\",\n        \"output\": \" Yes, CeCu7Ag2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4Co37B9\\n\",\n        \"output\": \" Yes, Ti4Co37B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe59Mo17C24\\n\",\n        \"output\": \" Yes, Fe59Mo17C24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si10Ni73B17\\n\",\n        \"output\": \" Yes, Si10Ni73B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2Mg13Zn5\\n\",\n        \"output\": \" Yes, La2Mg13Zn5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiAl4\\n\",\n        \"output\": \" No, TiAl4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co7W2C\\n\",\n        \"output\": \" No, Co7W2C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca7Al3\\n\",\n        \"output\": \" Yes, Ca7Al3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni19B6\\n\",\n        \"output\": \" No, Ni19B6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10V0.09Fe89.91\\n\",\n        \"output\": \" Yes, Zr10V0.09Fe89.91 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V25Co63.75B11.25\\n\",\n        \"output\": \" Yes, V25Co63.75B11.25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce6Cu89Ag5\\n\",\n        \"output\": \" No, Ce6Cu89Ag5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdAl86Ni13\\n\",\n        \"output\": \" Yes, NdAl86Ni13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf2CuNi7\\n\",\n        \"output\": \" Yes, Hf2CuNi7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti57.5Nb25Si17.5\\n\",\n        \"output\": \" Yes, Ti57.5Nb25Si17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr15Al17Ni18\\n\",\n        \"output\": \" Yes, Zr15Al17Ni18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni40B9P\\n\",\n        \"output\": \" Yes, Ni40B9P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80.5B17Mo2.5\\n\",\n        \"output\": \" Yes, Fe80.5B17Mo2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni37B59C4\\n\",\n        \"output\": \" Yes, Ni37B59C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La11Al7Cu2\\n\",\n        \"output\": \" Yes, La11Al7Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co15W2C3\\n\",\n        \"output\": \" No, Co15W2C3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn17Fe5B3\\n\",\n        \"output\": \" No, Mn17Fe5B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6VCu3\\n\",\n        \"output\": \" Yes, Al6VCu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe22Ni59B19\\n\",\n        \"output\": \" Yes, Fe22Ni59B19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn9Co75B16\\n\",\n        \"output\": \" Yes, Mn9Co75B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4Al5Cu\\n\",\n        \"output\": \" No, La4Al5Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti13(Al15Ni14)3\\n\",\n        \"output\": \" Yes, Ti13(Al15Ni14)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Fe3\\n\",\n        \"output\": \" Yes, Nd2Fe3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe39Ni39B22\\n\",\n        \"output\": \" Yes, Fe39Ni39B22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni37B55C8\\n\",\n        \"output\": \" Yes, Ni37B55C8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti17Al33\\n\",\n        \"output\": \" Yes, Ti17Al33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe16PC3\\n\",\n        \"output\": \" No, Fe16PC3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Yb9Cu41\\n\",\n        \"output\": \" Yes, Yb9Cu41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co3B\\n\",\n        \"output\": \" Yes, Co3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti5Al7Cu8\\n\",\n        \"output\": \" No, Ti5Al7Cu8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni35B11C4\\n\",\n        \"output\": \" No, Ni35B11C4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr14Al13Ni23\\n\",\n        \"output\": \" Yes, Zr14Al13Ni23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.9Ti0.1Ni33\\n\",\n        \"output\": \" Yes, Zr66.9Ti0.1Ni33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2(Mg5Cu)3\\n\",\n        \"output\": \" Yes, Nd2(Mg5Cu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce18Al67Fe15\\n\",\n        \"output\": \" No, Ce18Al67Fe15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La28Al55Ni17\\n\",\n        \"output\": \" Yes, La28Al55Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co23(Mo2C)9\\n\",\n        \"output\": \" Yes, Co23(Mo2C)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu8Si16.2Pd75.8\\n\",\n        \"output\": \" Yes, Cu8Si16.2Pd75.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al12Cr3Si5\\n\",\n        \"output\": \" Yes, Al12Cr3Si5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn21.6Co50.4B28\\n\",\n        \"output\": \" Yes, Mn21.6Co50.4B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" meal\\n\",\n        \"output\": \" meal is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti27Al5Ni18\\n\",\n        \"output\": \" Yes, Ti27Al5Ni18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr11Co9C5\\n\",\n        \"output\": \" Yes, Cr11Co9C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al9Si8\\n\",\n        \"output\": \" No, Mn3Al9Si8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al41Fe2Ni7\\n\",\n        \"output\": \" No, Al41Fe2Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr16La47Cu37\\n\",\n        \"output\": \" Yes, Sr16La47Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Al6Ni\\n\",\n        \"output\": \" No, Zr3Al6Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al65(Fe3Ni2)7\\n\",\n        \"output\": \" No, Al65(Fe3Ni2)7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe61.5Ni22B16.5\\n\",\n        \"output\": \" Yes, Fe61.5Ni22B16.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al22CoNi2\\n\",\n        \"output\": \" Yes, Al22CoNi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe78B9P13\\n\",\n        \"output\": \" Yes, Fe78B9P13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y13Al87\\n\",\n        \"output\": \" Yes, Y13Al87 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr6Co14C5\\n\",\n        \"output\": \" No, Cr6Co14C5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Al43Ni4\\n\",\n        \"output\": \" Yes, Nd3Al43Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd7Mg10Ni3\\n\",\n        \"output\": \" Yes, Nd7Mg10Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4CrNi5\\n\",\n        \"output\": \" Yes, Zr4CrNi5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe33B12N5\\n\",\n        \"output\": \" Yes, Fe33B12N5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co75Si12.5B12.5\\n\",\n        \"output\": \" Yes, Co75Si12.5B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YAl18Ni\\n\",\n        \"output\": \" Yes, YAl18Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15.6Co76.4W8\\n\",\n        \"output\": \" Yes, Zr15.6Co76.4W8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni18B7\\n\",\n        \"output\": \" Yes, Ni18B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si14Ni67B19\\n\",\n        \"output\": \" No, Si14Ni67B19 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg13Al2Zn5\\n\",\n        \"output\": \" Yes, Mg13Al2Zn5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti4Al9Cu7\\n\",\n        \"output\": \" No, Ti4Al9Cu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe44Ni5B\\n\",\n        \"output\": \" No, Fe44Ni5B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79B16P5\\n\",\n        \"output\": \" Yes, Fe79B16P5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3BeNb\\n\",\n        \"output\": \" No, Zr3BeNb does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6.5V10Co83.5\\n\",\n        \"output\": \" Yes, Zr6.5V10Co83.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83Si3B14\\n\",\n        \"output\": \" Yes, Fe83Si3B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" BMo8P\\n\",\n        \"output\": \" Yes, BMo8P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co13(B2C)4\\n\",\n        \"output\": \" Yes, Co13(B2C)4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79B13P8\\n\",\n        \"output\": \" Yes, Fe79B13P8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zn29Cu70Pb\\n\",\n        \"output\": \" Yes, Zn29Cu70Pb has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti28(Nb5Cu19)3\\n\",\n        \"output\": \" Yes, Ti28(Nb5Cu19)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6Co29B15\\n\",\n        \"output\": \" Yes, Al6Co29B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Tb15Fe76.5Co8.5\\n\",\n        \"output\": \" Yes, Tb15Fe76.5Co8.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg77Ti23\\n\",\n        \"output\": \" No, Mg77Ti23 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce6Cu69Ag25\\n\",\n        \"output\": \" Yes, Ce6Cu69Ag25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce2MnAl17\\n\",\n        \"output\": \" Yes, Ce2MnAl17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al89Co3Ni8\\n\",\n        \"output\": \" No, Al89Co3Ni8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe7BMo2\\n\",\n        \"output\": \" Yes, Fe7BMo2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf3CuNi6\\n\",\n        \"output\": \" Yes, Hf3CuNi6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Mg6Ni\\n\",\n        \"output\": \" Yes, Nd3Mg6Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf42.6Nb1Cu56.4\\n\",\n        \"output\": \" Yes, Hf42.6Nb1Cu56.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10Al0.018Fe89.982\\n\",\n        \"output\": \" Yes, Zr10Al0.018Fe89.982 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn(Fe29B4)3\\n\",\n        \"output\": \" No, Mn(Fe29B4)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co7SiC2\\n\",\n        \"output\": \" No, Co7SiC2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" care\\n\",\n        \"output\": \" care is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe40B7P3\\n\",\n        \"output\": \" Yes, Fe40B7P3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sr14La49Cu37\\n\",\n        \"output\": \" Yes, Sr14La49Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr6Fe17B2\\n\",\n        \"output\": \" No, Cr6Fe17B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr13Cr4Si3\\n\",\n        \"output\": \" Yes, Zr13Cr4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ge21Pd79\\n\",\n        \"output\": \" Yes, Ge21Pd79 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Ni10Pd73.5\\n\",\n        \"output\": \" Yes, Si16.5Ni10Pd73.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti5Al4Cu\\n\",\n        \"output\": \" No, Ti5Al4Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y2.5Mg91.5Mn6\\n\",\n        \"output\": \" Yes, Y2.5Mg91.5Mn6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr83Al11Ni6\\n\",\n        \"output\": \" Yes, Zr83Al11Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf5Zr52Be43\\n\",\n        \"output\": \" Yes, Hf5Zr52Be43 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd(Al7Ni)3\\n\",\n        \"output\": \" Yes, Nd(Al7Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2TiSi2\\n\",\n        \"output\": \" Yes, Zr2TiSi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SiB2Mo7\\n\",\n        \"output\": \" Yes, SiB2Mo7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si2(BMo5)3\\n\",\n        \"output\": \" Yes, Si2(BMo5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co25Mo18C7\\n\",\n        \"output\": \" No, Co25Mo18C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe4.2Si16.5Pd79.3\\n\",\n        \"output\": \" Yes, Fe4.2Si16.5Pd79.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdFe9\\n\",\n        \"output\": \" Yes, NdFe9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg8Cu\\n\",\n        \"output\": \" Yes, CeMg8Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8Fe89.5B2.5\\n\",\n        \"output\": \" Yes, Zr8Fe89.5B2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y5(Mg14Mn)3\\n\",\n        \"output\": \" Yes, Y5(Mg14Mn)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd6Fe75.5B18.5\\n\",\n        \"output\": \" Yes, Nd6Fe75.5B18.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce5(Mg4Ni)9\\n\",\n        \"output\": \" Yes, Ce5(Mg4Ni)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y3Al14Ni3\\n\",\n        \"output\": \" Yes, Y3Al14Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15Co67Mo18\\n\",\n        \"output\": \" Yes, Zr15Co67Mo18 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Ti4Si9\\n\",\n        \"output\": \" Yes, Zr7Ti4Si9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr11Al4Ni5\\n\",\n        \"output\": \" Yes, Zr11Al4Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5Mg11Cu4\\n\",\n        \"output\": \" Yes, Nd5Mg11Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb3Fe12Co5\\n\",\n        \"output\": \" Yes, Nb3Fe12Co5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La37Al55Ni8\\n\",\n        \"output\": \" Yes, La37Al55Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg6Ti61Al33\\n\",\n        \"output\": \" Yes, Mg6Ti61Al33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr44Ti17Cu39\\n\",\n        \"output\": \" Yes, Zr44Ti17Cu39 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5(Fe13B2)3\\n\",\n        \"output\": \" Yes, Cr5(Fe13B2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Ti4Ge3\\n\",\n        \"output\": \" Yes, Zr13Ti4Ge3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr17(Co8C3)3\\n\",\n        \"output\": \" Yes, Cr17(Co8C3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr6Fe43B\\n\",\n        \"output\": \" No, Cr6Fe43B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al23Fe2\\n\",\n        \"output\": \" No, Al23Fe2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr16(AlNi)17\\n\",\n        \"output\": \" Yes, Zr16(AlNi)17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si4B3Mo13\\n\",\n        \"output\": \" No, Si4B3Mo13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr10Fe89.946Ge0.054\\n\",\n        \"output\": \" Yes, Zr10Fe89.946Ge0.054 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13Be6Nb\\n\",\n        \"output\": \" Yes, Zr13Be6Nb has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Be3\\n\",\n        \"output\": \" Yes, Zr7Be3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79B16Mo5\\n\",\n        \"output\": \" Yes, Fe79B16Mo5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr49Ni49P2\\n\",\n        \"output\": \" Yes, Zr49Ni49P2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si12Ni67B21\\n\",\n        \"output\": \" Yes, Si12Ni67B21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" HfCu4Ni5\\n\",\n        \"output\": \" No, HfCu4Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe51Cu23Ag26\\n\",\n        \"output\": \" No, Fe51Cu23Ag26 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr(Fe5B)4\\n\",\n        \"output\": \" Yes, Zr(Fe5B)4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn15.2Co60.8B24\\n\",\n        \"output\": \" Yes, Mn15.2Co60.8B24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Be2Fe7B\\n\",\n        \"output\": \" Yes, Be2Fe7B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr2.5Fe80.5B17\\n\",\n        \"output\": \" Yes, Cr2.5Fe80.5B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CrFe79B20\\n\",\n        \"output\": \" Yes, CrFe79B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiNi9\\n\",\n        \"output\": \" No, TiNi9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd7.5Mg92.5\\n\",\n        \"output\": \" No, Nd7.5Mg92.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Al22Ni\\n\",\n        \"output\": \" Yes, Nd2Al22Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni16Mo7C2\\n\",\n        \"output\": \" No, Ni16Mo7C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg11Zn9\\n\",\n        \"output\": \" No, Mg11Zn9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce(MgNi)2\\n\",\n        \"output\": \" No, Ce(MgNi)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y12.5Mg87.5\\n\",\n        \"output\": \" No, Y12.5Mg87.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn26.6Co49.4B24\\n\",\n        \"output\": \" Yes, Mn26.6Co49.4B24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe37Cu41Ag22\\n\",\n        \"output\": \" No, Fe37Cu41Ag22 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Co81Mo14\\n\",\n        \"output\": \" Yes, Zr5Co81Mo14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr12Fe75B13\\n\",\n        \"output\": \" Yes, Zr12Fe75B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe16B3C\\n\",\n        \"output\": \" Yes, Fe16B3C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe72.5Si12.5B15\\n\",\n        \"output\": \" Yes, Fe72.5Si12.5B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn3Fe81B16\\n\",\n        \"output\": \" Yes, Mn3Fe81B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2(CuAu)9\\n\",\n        \"output\": \" Yes, La2(CuAu)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Co43B5\\n\",\n        \"output\": \" No, Al2Co43B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdAl45Ni4\\n\",\n        \"output\": \" Yes, NdAl45Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co3.5Ni75.5P21\\n\",\n        \"output\": \" Yes, Co3.5Ni75.5P21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al45CoNi4\\n\",\n        \"output\": \" No, Al45CoNi4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al(NiB)2\\n\",\n        \"output\": \" Yes, Al(NiB)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si18Pd77Au5\\n\",\n        \"output\": \" Yes, Si18Pd77Au5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" cabinet\\n\",\n        \"output\": \" cabinet is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al22Cr3\\n\",\n        \"output\": \" No, Al22Cr3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y4Mg21\\n\",\n        \"output\": \" Yes, Y4Mg21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr11(Fe11B2)3\\n\",\n        \"output\": \" Yes, Cr11(Fe11B2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca7.5Al90Ni2.5\\n\",\n        \"output\": \" Yes, Ca7.5Al90Ni2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni16B5C4\\n\",\n        \"output\": \" Yes, Ni16B5C4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg2Al2Zn\\n\",\n        \"output\": \" No, Mg2Al2Zn does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiAl2Ni\\n\",\n        \"output\": \" Yes, TiAl2Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Fe16B\\n\",\n        \"output\": \" Yes, Zr3Fe16B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu84.5Ag9P6.5\\n\",\n        \"output\": \" No, Cu84.5Ag9P6.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe80B9P11\\n\",\n        \"output\": \" Yes, Fe80B9P11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr16Cu3B\\n\",\n        \"output\": \" Yes, Zr16Cu3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti8Co31B11\\n\",\n        \"output\": \" Yes, Ti8Co31B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni37B10C3\\n\",\n        \"output\": \" No, Ni37B10C3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" bottom\\n\",\n        \"output\": \" bottom is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg18Cu\\n\",\n        \"output\": \" No, YMg18Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al70Si17Ni13\\n\",\n        \"output\": \" Yes, Al70Si17Ni13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg7(Ti18Al13)3\\n\",\n        \"output\": \" Yes, Mg7(Ti18Al13)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti6Al9Ni5\\n\",\n        \"output\": \" Yes, Ti6Al9Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr20(Fe7C3)3\\n\",\n        \"output\": \" Yes, Cr20(Fe7C3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe19BMo5\\n\",\n        \"output\": \" No, Fe19BMo5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg3Ti20Al77\\n\",\n        \"output\": \" No, Mg3Ti20Al77 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83B17\\n\",\n        \"output\": \" Yes, Fe83B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y(Mg28Cu5)3\\n\",\n        \"output\": \" No, Y(Mg28Cu5)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2MgCu7\\n\",\n        \"output\": \" No, Nd2MgCu7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Ti3Cu5\\n\",\n        \"output\": \" Yes, Zr2Ti3Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" rocket\\n\",\n        \"output\": \" rocket is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Cu\\n\",\n        \"output\": \" No, Ti9Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe27Cu51Ag22\\n\",\n        \"output\": \" No, Fe27Cu51Ag22 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Cu7\\n\",\n        \"output\": \" No, Nd3Cu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl9\\n\",\n        \"output\": \" Yes, CeAl9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn43Co37B20\\n\",\n        \"output\": \" Yes, Mn43Co37B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13Ti3Si4\\n\",\n        \"output\": \" Yes, Zr13Ti3Si4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Mg15Ni2\\n\",\n        \"output\": \" Yes, Ce3Mg15Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co17SiC2\\n\",\n        \"output\": \" No, Co17SiC2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd2Al17Ni\\n\",\n        \"output\": \" Yes, Gd2Al17Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43Cr7\\n\",\n        \"output\": \" No, Al43Cr7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al72Fe13Ni15\\n\",\n        \"output\": \" No, Al72Fe13Ni15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe70Si17.5C12.5\\n\",\n        \"output\": \" Yes, Fe70Si17.5C12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti5(Nb4Si)3\\n\",\n        \"output\": \" Yes, Ti5(Nb4Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti67Ni33\\n\",\n        \"output\": \" Yes, Ti67Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y7.5Mg84.5Mn8\\n\",\n        \"output\": \" No, Y7.5Mg84.5Mn8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni31B14C5\\n\",\n        \"output\": \" Yes, Ni31B14C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Cu3\\n\",\n        \"output\": \" No, Ti7Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co17B5C3\\n\",\n        \"output\": \" Yes, Co17B5C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca1La61.5Cu37.5\\n\",\n        \"output\": \" Yes, Ca1La61.5Cu37.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr56.95Co15Ni28.05\\n\",\n        \"output\": \" Yes, Zr56.95Co15Ni28.05 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti10Cu3Ni7\\n\",\n        \"output\": \" No, Ti10Cu3Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al89Fe7Ni4\\n\",\n        \"output\": \" No, Al89Fe7Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SiNi17B7\\n\",\n        \"output\": \" Yes, SiNi17B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al59Ni10Ge31\\n\",\n        \"output\": \" Yes, Al59Ni10Ge31 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr23Co20C7\\n\",\n        \"output\": \" No, Cr23Co20C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu3Ni81P16\\n\",\n        \"output\": \" No, Cu3Ni81P16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn31(Co19B4)3\\n\",\n        \"output\": \" Yes, Mn31(Co19B4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6Cu13B\\n\",\n        \"output\": \" Yes, Zr6Cu13B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" cello\\n\",\n        \"output\": \" cello is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si2Ni16B7\\n\",\n        \"output\": \" No, Si2Ni16B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2Al3Ni5\\n\",\n        \"output\": \" No, Zr2Al3Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti22Al53Ni25\\n\",\n        \"output\": \" Yes, Ti22Al53Ni25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al43Co7\\n\",\n        \"output\": \" No, Al43Co7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr67Co33\\n\",\n        \"output\": \" Yes, Zr67Co33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeCu13Ag6\\n\",\n        \"output\": \" No, CeCu13Ag6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La8Mg7Cu5\\n\",\n        \"output\": \" Yes, La8Mg7Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79B11P10\\n\",\n        \"output\": \" Yes, Fe79B11P10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Al86Ni9\\n\",\n        \"output\": \" Yes, Zr5Al86Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al14VGe5\\n\",\n        \"output\": \" No, Al14VGe5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl44Ni5\\n\",\n        \"output\": \" Yes, NdAl44Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Co83Mo12\\n\",\n        \"output\": \" Yes, Zr5Co83Mo12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3Ni69B28\\n\",\n        \"output\": \" Yes, Si3Ni69B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe81Co2B17\\n\",\n        \"output\": \" Yes, Fe81Co2B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2VNi2\\n\",\n        \"output\": \" Yes, Zr2VNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd4Fe19B2\\n\",\n        \"output\": \" Yes, Nd4Fe19B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe21Ni62B17\\n\",\n        \"output\": \" Yes, Fe21Ni62B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Al35Ni8\\n\",\n        \"output\": \" Yes, Zr7Al35Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrAlNi3\\n\",\n        \"output\": \" No, ZrAlNi3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Al22\\n\",\n        \"output\": \" Yes, Nd3Al22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79CuB20\\n\",\n        \"output\": \" No, Fe79CuB20 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg3Zn\\n\",\n        \"output\": \" Yes, Mg3Zn has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2CuNi\\n\",\n        \"output\": \" Yes, Ti2CuNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Cu12B\\n\",\n        \"output\": \" Yes, Zr7Cu12B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeCu7Ag12\\n\",\n        \"output\": \" No, CeCu7Ag12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr15Co26C9\\n\",\n        \"output\": \" Yes, Cr15Co26C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr39Cu60B\\n\",\n        \"output\": \" Yes, Zr39Cu60B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr17(SiNi3)2\\n\",\n        \"output\": \" Yes, Zr17(SiNi3)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al91Co2Ni7\\n\",\n        \"output\": \" No, Al91Co2Ni7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sm7Al83Ni10\\n\",\n        \"output\": \" Yes, Sm7Al83Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr17Cr12Co71\\n\",\n        \"output\": \" Yes, Zr17Cr12Co71 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6Al5Ni9\\n\",\n        \"output\": \" Yes, Zr6Al5Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al86Co5Ni9\\n\",\n        \"output\": \" No, Al86Co5Ni9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti\\n\",\n        \"output\": \" No, Ti does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca2.5Al92.5Ni5\\n\",\n        \"output\": \" No, Ca2.5Al92.5Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Al90Ni7\\n\",\n        \"output\": \" Yes, Nd3Al90Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al48CoNi\\n\",\n        \"output\": \" No, Al48CoNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf69V16Si15\\n\",\n        \"output\": \" Yes, Hf69V16Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe15P4C\\n\",\n        \"output\": \" Yes, Fe15P4C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" committee\\n\",\n        \"output\": \" committee is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La10Al3Ni7\\n\",\n        \"output\": \" Yes, La10Al3Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ni43.4Pd40.1\\n\",\n        \"output\": \" Yes, Si16.5Ni43.4Pd40.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" pillow\\n\",\n        \"output\": \" pillow is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca4La58.5Cu37.5\\n\",\n        \"output\": \" Yes, Ca4La58.5Cu37.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr7Ni34P9\\n\",\n        \"output\": \" Yes, Cr7Ni34P9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe42Cu31Ag27\\n\",\n        \"output\": \" No, Fe42Cu31Ag27 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca7.5Mg92.5\\n\",\n        \"output\": \" No, Ca7.5Mg92.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti15Be3Si2\\n\",\n        \"output\": \" No, Ti15Be3Si2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg15Al2Zn3\\n\",\n        \"output\": \" Yes, Mg15Al2Zn3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb15Fe6Co79\\n\",\n        \"output\": \" Yes, Nb15Fe6Co79 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al78Fe7Cu15\\n\",\n        \"output\": \" No, Al78Fe7Cu15 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al9Cr3Si8\\n\",\n        \"output\": \" No, Al9Cr3Si8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Al14Ni3\\n\",\n        \"output\": \" No, La3Al14Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al87V8Cu5\\n\",\n        \"output\": \" No, Al87V8Cu5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni33B9C8\\n\",\n        \"output\": \" Yes, Ni33B9C8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr38Nb5Cu57\\n\",\n        \"output\": \" Yes, Zr38Nb5Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41W4C5\\n\",\n        \"output\": \" No, Fe41W4C5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr40(FeCu19)3\\n\",\n        \"output\": \" Yes, Zr40(FeCu19)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb15Fe12Co73\\n\",\n        \"output\": \" Yes, Nb15Fe12Co73 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" libra\\n\",\n        \"output\": \" libra is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" bit\\n\",\n        \"output\": \" bit is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg41Ti50Al9\\n\",\n        \"output\": \" No, Mg41Ti50Al9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y4(MgAg)3\\n\",\n        \"output\": \" Yes, Y4(MgAg)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15(Ni3B2)2\\n\",\n        \"output\": \" Yes, Zr15(Ni3B2)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAlNi8\\n\",\n        \"output\": \" No, LaAlNi8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti11(SiNi2)3\\n\",\n        \"output\": \" Yes, Ti11(SiNi2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ni1.7Pd81.8\\n\",\n        \"output\": \" Yes, Si16.5Ni1.7Pd81.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni17B23C10\\n\",\n        \"output\": \" Yes, Ni17B23C10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg3Ti7Al10\\n\",\n        \"output\": \" Yes, Mg3Ti7Al10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni5(PPd4)19\\n\",\n        \"output\": \" Yes, Ni5(PPd4)19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7VSi2\\n\",\n        \"output\": \" Yes, Ti7VSi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr66.85Cu33Ni0.15\\n\",\n        \"output\": \" Yes, Zr66.85Cu33Ni0.15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ni58.5Pd25\\n\",\n        \"output\": \" No, Si16.5Ni58.5Pd25 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu5.8Si19.5Pd74.7\\n\",\n        \"output\": \" Yes, Cu5.8Si19.5Pd74.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu73Ag27\\n\",\n        \"output\": \" No, Cu73Ag27 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg5Cu2\\n\",\n        \"output\": \" Yes, Nd3Mg5Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe73(SiB8)3\\n\",\n        \"output\": \" No, Fe73(SiB8)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al57Cr28Si15\\n\",\n        \"output\": \" No, Al57Cr28Si15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr34.4Nb20Cu45.6\\n\",\n        \"output\": \" Yes, Zr34.4Nb20Cu45.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe85(CuB4)3\\n\",\n        \"output\": \" No, Fe85(CuB4)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe10Si16.5Pd73.5\\n\",\n        \"output\": \" Yes, Fe10Si16.5Pd73.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2Fe18B5\\n\",\n        \"output\": \" Yes, Mn2Fe18B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81B8P11\\n\",\n        \"output\": \" Yes, Fe81B8P11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrFe45B4\\n\",\n        \"output\": \" No, ZrFe45B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrNb7Si2\\n\",\n        \"output\": \" Yes, ZrNb7Si2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf3Cu6Ni\\n\",\n        \"output\": \" Yes, Hf3Cu6Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y(Mg23Cu10)3\\n\",\n        \"output\": \" Yes, Y(Mg23Cu10)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr46.9Mn30Ni23.1\\n\",\n        \"output\": \" Yes, Zr46.9Mn30Ni23.1 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr35(SiNi4)3\\n\",\n        \"output\": \" Yes, Zr35(SiNi4)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La4Mg5Cu\\n\",\n        \"output\": \" No, La4Mg5Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnAl2Si\\n\",\n        \"output\": \" No, MnAl2Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg23Ti20Al7\\n\",\n        \"output\": \" No, Mg23Ti20Al7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CrFe8B\\n\",\n        \"output\": \" No, CrFe8B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al15Cr2Si3\\n\",\n        \"output\": \" No, Al15Cr2Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe93CuB6\\n\",\n        \"output\": \" No, Fe93CuB6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ceramic\\n\",\n        \"output\": \" ceramic is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe35(B2Mo3)3\\n\",\n        \"output\": \" Yes, Fe35(B2Mo3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr2Fe18P5\\n\",\n        \"output\": \" Yes, Cr2Fe18P5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87Co5Ni8\\n\",\n        \"output\": \" No, Al87Co5Ni8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr4Fe20B\\n\",\n        \"output\": \" No, Cr4Fe20B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Al33Ni14\\n\",\n        \"output\": \" Yes, La3Al33Ni14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr12Fe35B3\\n\",\n        \"output\": \" No, Cr12Fe35B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Nb10Si3\\n\",\n        \"output\": \" Yes, Zr7Nb10Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf11(Zr2Si)3\\n\",\n        \"output\": \" Yes, Hf11(Zr2Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg3Ni4\\n\",\n        \"output\": \" Yes, Y3Mg3Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y2.5Mg89.5Mn8\\n\",\n        \"output\": \" No, Y2.5Mg89.5Mn8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe15B4\\n\",\n        \"output\": \" Yes, ZrFe15B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Co37B11\\n\",\n        \"output\": \" Yes, Al2Co37B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.9Cr33Ni0.1\\n\",\n        \"output\": \" Yes, Zr66.9Cr33Ni0.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La15AlNi4\\n\",\n        \"output\": \" Yes, La15AlNi4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd5(Mg3Cu2)3\\n\",\n        \"output\": \" Yes, Nd5(Mg3Cu2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Al17Co\\n\",\n        \"output\": \" Yes, Ce2Al17Co has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7Cu2Ni\\n\",\n        \"output\": \" Yes, Ti7Cu2Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl47V2\\n\",\n        \"output\": \" No, CeAl47V2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe65Si22.5C12.5\\n\",\n        \"output\": \" Yes, Fe65Si22.5C12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si3B2Mo15\\n\",\n        \"output\": \" Yes, Si3B2Mo15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni38B5P7\\n\",\n        \"output\": \" Yes, Ni38B5P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" snail\\n\",\n        \"output\": \" snail is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co5Ni78P17\\n\",\n        \"output\": \" No, Co5Ni78P17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Fe89B4\\n\",\n        \"output\": \" Yes, Zr7Fe89B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11Cu5Ni4\\n\",\n        \"output\": \" Yes, Zr11Cu5Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg35(Zn4In)3\\n\",\n        \"output\": \" Yes, Mg35(Zn4In)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr39Ni28Mo33\\n\",\n        \"output\": \" Yes, Cr39Ni28Mo33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAl43Ni6\\n\",\n        \"output\": \" Yes, LaAl43Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnCo3B\\n\",\n        \"output\": \" Yes, MnCo3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4Ti5Cu11\\n\",\n        \"output\": \" Yes, Zr4Ti5Cu11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3Ni15B2\\n\",\n        \"output\": \" Yes, Si3Ni15B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr16.3Co75.7Mo8\\n\",\n        \"output\": \" Yes, Zr16.3Co75.7Mo8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr12Cr12.6Co75.4\\n\",\n        \"output\": \" Yes, Zr12Cr12.6Co75.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti43Al57\\n\",\n        \"output\": \" Yes, Ti43Al57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83B10P7\\n\",\n        \"output\": \" Yes, Fe83B10P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7Ni2B\\n\",\n        \"output\": \" Yes, Ti7Ni2B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sr14.5La53.5Cu32\\n\",\n        \"output\": \" Yes, Sr14.5La53.5Cu32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr13Fe31B6\\n\",\n        \"output\": \" Yes, Cr13Fe31B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Al42Ni5\\n\",\n        \"output\": \" Yes, Nd3Al42Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co65Si7.5B27.5\\n\",\n        \"output\": \" Yes, Co65Si7.5B27.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr16AlNi3\\n\",\n        \"output\": \" Yes, Zr16AlNi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe43B3Mo4\\n\",\n        \"output\": \" No, Fe43B3Mo4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti4Al5Cu\\n\",\n        \"output\": \" No, Ti4Al5Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr7Fe79B14\\n\",\n        \"output\": \" Yes, Cr7Fe79B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti13Al2Cu5\\n\",\n        \"output\": \" Yes, Ti13Al2Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9.5Co85.5W5\\n\",\n        \"output\": \" Yes, Zr9.5Co85.5W5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg3AlZn\\n\",\n        \"output\": \" No, Mg3AlZn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba7.5La63.5Cu29\\n\",\n        \"output\": \" Yes, Ba7.5La63.5Cu29 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe80Si7P13\\n\",\n        \"output\": \" Yes, Fe80Si7P13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si17.5Ni67.5C15\\n\",\n        \"output\": \" Yes, Si17.5Ni67.5C15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti15Al13Ni22\\n\",\n        \"output\": \" Yes, Ti15Al13Ni22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La5Mg11Cu4\\n\",\n        \"output\": \" No, La5Mg11Cu4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn26.8Co40.2B33\\n\",\n        \"output\": \" Yes, Mn26.8Co40.2B33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe2Ni2P\\n\",\n        \"output\": \" Yes, Fe2Ni2P has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeCu8Ag\\n\",\n        \"output\": \" Yes, CeCu8Ag has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn4Al13Ge3\\n\",\n        \"output\": \" No, Mn4Al13Ge3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V7Fe79B14\\n\",\n        \"output\": \" Yes, V7Fe79B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti6Nb11Si3\\n\",\n        \"output\": \" Yes, Ti6Nb11Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb80Si17Ge3\\n\",\n        \"output\": \" Yes, Nb80Si17Ge3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe8Co75B17\\n\",\n        \"output\": \" Yes, Fe8Co75B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf16VSi3\\n\",\n        \"output\": \" Yes, Hf16VSi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr67Fe3.3Ni29.7\\n\",\n        \"output\": \" Yes, Zr67Fe3.3Ni29.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YAl7Ni2\\n\",\n        \"output\": \" Yes, YAl7Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe80P12.5C7.5\\n\",\n        \"output\": \" Yes, Fe80P12.5C7.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La6Al5Ni9\\n\",\n        \"output\": \" Yes, La6Al5Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" HfCu7Ni2\\n\",\n        \"output\": \" No, HfCu7Ni2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La6Al85Ni9\\n\",\n        \"output\": \" Yes, La6Al85Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2SiNi2\\n\",\n        \"output\": \" Yes, Ti2SiNi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn12Co8B5\\n\",\n        \"output\": \" Yes, Mn12Co8B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80Si11B9\\n\",\n        \"output\": \" No, Fe80Si11B9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" tramp\\n\",\n        \"output\": \" tramp is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La13Al5Cu2\\n\",\n        \"output\": \" Yes, La13Al5Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2Al47Ni\\n\",\n        \"output\": \" No, Mn2Al47Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al9Ni\\n\",\n        \"output\": \" No, Al9Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Cu10B\\n\",\n        \"output\": \" Yes, Zr9Cu10B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr3Co5B2\\n\",\n        \"output\": \" Yes, Cr3Co5B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg3Zn2\\n\",\n        \"output\": \" Yes, Mg3Zn2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg15Ni4\\n\",\n        \"output\": \" Yes, NdMg15Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr15Ni66P19\\n\",\n        \"output\": \" Yes, Cr15Ni66P19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si4Pd21\\n\",\n        \"output\": \" Yes, Si4Pd21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11.5Co74.5W14\\n\",\n        \"output\": \" Yes, Zr11.5Co74.5W14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sr6La57Cu37\\n\",\n        \"output\": \" Yes, Sr6La57Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La7Al11Ni2\\n\",\n        \"output\": \" No, La7Al11Ni2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe69Ni15B16\\n\",\n        \"output\": \" Yes, Fe69Ni15B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9Nb8Si3\\n\",\n        \"output\": \" Yes, Zr9Nb8Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn35Co53B12\\n\",\n        \"output\": \" Yes, Mn35Co53B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf84VSi15\\n\",\n        \"output\": \" Yes, Hf84VSi15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn9Co9B7\\n\",\n        \"output\": \" Yes, Mn9Co9B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7(V6Co25)3\\n\",\n        \"output\": \" Yes, Zr7(V6Co25)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sr3.5La59.5Cu37\\n\",\n        \"output\": \" Yes, Sr3.5La59.5Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Cu2\\n\",\n        \"output\": \" Yes, Zr3Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ga2Fe81B17\\n\",\n        \"output\": \" Yes, Ga2Fe81B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5V3Ni2\\n\",\n        \"output\": \" Yes, Zr5V3Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce10Al89Ni\\n\",\n        \"output\": \" Yes, Ce10Al89Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn30.5Co45.5B24\\n\",\n        \"output\": \" Yes, Mn30.5Co45.5B24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti16Cu3Ni\\n\",\n        \"output\": \" No, Ti16Cu3Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9Co91\\n\",\n        \"output\": \" Yes, Zr9Co91 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13(TiSi5)2\\n\",\n        \"output\": \" Yes, Zr13(TiSi5)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe83Si7B10\\n\",\n        \"output\": \" No, Fe83Si7B10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al89Co4Ni7\\n\",\n        \"output\": \" No, Al89Co4Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn17.4Al74.6Si8\\n\",\n        \"output\": \" No, Mn17.4Al74.6Si8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe21Cu6Ag23\\n\",\n        \"output\": \" Yes, Fe21Cu6Ag23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al11V2Ge7\\n\",\n        \"output\": \" Yes, Al11V2Ge7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe15Cu3B2\\n\",\n        \"output\": \" No, Fe15Cu3B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni25B23C2\\n\",\n        \"output\": \" No, Ni25B23C2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf4Zr13Si3\\n\",\n        \"output\": \" Yes, Hf4Zr13Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe40B9P\\n\",\n        \"output\": \" Yes, Fe40B9P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe73(Cu5B4)3\\n\",\n        \"output\": \" No, Fe73(Cu5B4)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La4(MgCu)3\\n\",\n        \"output\": \" Yes, La4(MgCu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9Al7Ni4\\n\",\n        \"output\": \" Yes, Zr9Al7Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La81AlNi18\\n\",\n        \"output\": \" Yes, La81AlNi18 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr66.8V0.2Ni33\\n\",\n        \"output\": \" Yes, Zr66.8V0.2Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr4La59Cu37\\n\",\n        \"output\": \" Yes, Sr4La59Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Al3Cu10\\n\",\n        \"output\": \" Yes, Ti7Al3Cu10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe29Ag21\\n\",\n        \"output\": \" No, Fe29Ag21 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf2Cu3Ni5\\n\",\n        \"output\": \" Yes, Hf2Cu3Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Al\\n\",\n        \"output\": \" No, La9Al does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Al10Ni7\\n\",\n        \"output\": \" No, La3Al10Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn28.8Co43.2B28\\n\",\n        \"output\": \" Yes, Mn28.8Co43.2B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Al11\\n\",\n        \"output\": \" No, Ti9Al11 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al14Cr5Si\\n\",\n        \"output\": \" No, Al14Cr5Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr56.95Ti15Ni28.05\\n\",\n        \"output\": \" Yes, Zr56.95Ti15Ni28.05 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Gd7(Al29Ni2)3\\n\",\n        \"output\": \" Yes, Gd7(Al29Ni2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe18W2C5\\n\",\n        \"output\": \" No, Fe18W2C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr87Si13\\n\",\n        \"output\": \" Yes, Zr87Si13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti28Nb47Si25\\n\",\n        \"output\": \" No, Ti28Nb47Si25 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn13.6Co54.4B32\\n\",\n        \"output\": \" Yes, Mn13.6Co54.4B32 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti36.6Nb15Cu48.4\\n\",\n        \"output\": \" Yes, Ti36.6Nb15Cu48.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn19Co19B12\\n\",\n        \"output\": \" Yes, Mn19Co19B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si9.45Ge13.66Au76.89\\n\",\n        \"output\": \" Yes, Si9.45Ge13.66Au76.89 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co74.5W7.5C18\\n\",\n        \"output\": \" No, Co74.5W7.5C18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co38W5C7\\n\",\n        \"output\": \" No, Co38W5C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe81.5P15C3.5\\n\",\n        \"output\": \" Yes, Fe81.5P15C3.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu15Si16Pd69\\n\",\n        \"output\": \" Yes, Cu15Si16Pd69 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Ti14Si3\\n\",\n        \"output\": \" Yes, Zr3Ti14Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La5(Al14Ni)3\\n\",\n        \"output\": \" Yes, La5(Al14Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr17(Co2C)11\\n\",\n        \"output\": \" Yes, Cr17(Co2C)11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti27Al23\\n\",\n        \"output\": \" Yes, Ti27Al23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7.7Fe78.1B14.2\\n\",\n        \"output\": \" Yes, Nb7.7Fe78.1B14.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr67(Al9Ni2)3\\n\",\n        \"output\": \" Yes, Zr67(Al9Ni2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe83Si5B12\\n\",\n        \"output\": \" Yes, Fe83Si5B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3CuNi\\n\",\n        \"output\": \" Yes, Ti3CuNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe23Cu27\\n\",\n        \"output\": \" No, Fe23Cu27 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr40(Ti7Cu13)3\\n\",\n        \"output\": \" Yes, Zr40(Ti7Cu13)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co18WC\\n\",\n        \"output\": \" No, Co18WC does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B14C5\\n\",\n        \"output\": \" Yes, Fe81B14C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg89Cu10\\n\",\n        \"output\": \" No, YMg89Cu10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe4(CuAg)3\\n\",\n        \"output\": \" Yes, Fe4(CuAg)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe73Ni25B2\\n\",\n        \"output\": \" No, Fe73Ni25B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co16B8C\\n\",\n        \"output\": \" Yes, Co16B8C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" raven\\n\",\n        \"output\": \" raven is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al4Ni35B11\\n\",\n        \"output\": \" Yes, Al4Ni35B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr8Cu11B\\n\",\n        \"output\": \" Yes, Zr8Cu11B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti2.1Ni78.8B19.1\\n\",\n        \"output\": \" Yes, Ti2.1Ni78.8B19.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" diamond\\n\",\n        \"output\": \" diamond is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al13Fe4Cu3\\n\",\n        \"output\": \" Yes, Al13Fe4Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ni29.2Pd54.3\\n\",\n        \"output\": \" Yes, Si16.5Ni29.2Pd54.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4Ni21\\n\",\n        \"output\": \" No, Ti4Ni21 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" HfFe\\n\",\n        \"output\": \" Yes, HfFe has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co8WC\\n\",\n        \"output\": \" No, Co8WC does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn5Fe81B14\\n\",\n        \"output\": \" Yes, Mn5Fe81B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Al17Ni24\\n\",\n        \"output\": \" Yes, La9Al17Ni24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe7B2Mo\\n\",\n        \"output\": \" Yes, Fe7B2Mo has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2(Mg5Ni)3\\n\",\n        \"output\": \" Yes, La2(Mg5Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr9La62.5Cu28.5\\n\",\n        \"output\": \" Yes, Sr9La62.5Cu28.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CuNi19P5\\n\",\n        \"output\": \" Yes, CuNi19P5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe67Si13B20\\n\",\n        \"output\": \" Yes, Fe67Si13B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni31B13C6\\n\",\n        \"output\": \" Yes, Ni31B13C6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Mg4Ni3\\n\",\n        \"output\": \" Yes, Nd3Mg4Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CrNi7B2\\n\",\n        \"output\": \" Yes, CrNi7B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe82Sn1.5B16.5\\n\",\n        \"output\": \" Yes, Fe82Sn1.5B16.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7Fe91B2\\n\",\n        \"output\": \" Yes, Zr7Fe91B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni33B14C3\\n\",\n        \"output\": \" Yes, Ni33B14C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe33Ni10B7\\n\",\n        \"output\": \" Yes, Fe33Ni10B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu15Si16.5Pd68.5\\n\",\n        \"output\": \" Yes, Cu15Si16.5Pd68.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd10Fe82.5B7.5\\n\",\n        \"output\": \" Yes, Nd10Fe82.5B7.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr13Fe32B5\\n\",\n        \"output\": \" Yes, Cr13Fe32B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5(Fe13B2)3\\n\",\n        \"output\": \" Yes, Zr5(Fe13B2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Al4Ni3\\n\",\n        \"output\": \" Yes, La3Al4Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Co18B5\\n\",\n        \"output\": \" Yes, Ti2Co18B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaMg8Ni\\n\",\n        \"output\": \" Yes, LaMg8Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Mg13Ni4\\n\",\n        \"output\": \" Yes, La3Mg13Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg92.5Mn7.5\\n\",\n        \"output\": \" No, Mg92.5Mn7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" HfCu\\n\",\n        \"output\": \" Yes, HfCu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr23(Fe5P2)11\\n\",\n        \"output\": \" Yes, Cr23(Fe5P2)11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu3Ni37P10\\n\",\n        \"output\": \" Yes, Cu3Ni37P10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si9Pd38Au3\\n\",\n        \"output\": \" Yes, Si9Pd38Au3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrAl17Ni2\\n\",\n        \"output\": \" Yes, ZrAl17Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Al2Ni9\\n\",\n        \"output\": \" Yes, La9Al2Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Ti2Si3\\n\",\n        \"output\": \" Yes, Zr5Ti2Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe75Si12.5B12.5\\n\",\n        \"output\": \" Yes, Fe75Si12.5B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe74.8Si13B12.2\\n\",\n        \"output\": \" Yes, Fe74.8Si13B12.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr12Al5Ni3\\n\",\n        \"output\": \" Yes, Zr12Al5Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf44Nb41Si15\\n\",\n        \"output\": \" Yes, Hf44Nb41Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn49Co35B16\\n\",\n        \"output\": \" Yes, Mn49Co35B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce5Al7Cu38\\n\",\n        \"output\": \" No, Ce5Al7Cu38 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co15Si2B3\\n\",\n        \"output\": \" Yes, Co15Si2B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79(SiB2)7\\n\",\n        \"output\": \" Yes, Fe79(SiB2)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2Mg7Ni\\n\",\n        \"output\": \" Yes, La2Mg7Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe75Si13B12\\n\",\n        \"output\": \" Yes, Fe75Si13B12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl40Ni9\\n\",\n        \"output\": \" Yes, NdAl40Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca7.5Mg87.5Zn5\\n\",\n        \"output\": \" No, Ca7.5Mg87.5Zn5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg17Cu3\\n\",\n        \"output\": \" No, Mg17Cu3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb8.7Fe76B15.3\\n\",\n        \"output\": \" Yes, Nb8.7Fe76B15.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti4Si\\n\",\n        \"output\": \" Yes, Ti4Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr63.65Ti5Ni31.35\\n\",\n        \"output\": \" Yes, Zr63.65Ti5Ni31.35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8(TiSi3)3\\n\",\n        \"output\": \" Yes, Zr8(TiSi3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2Mg2Ag\\n\",\n        \"output\": \" Yes, Y2Mg2Ag has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" GdAl7Ni2\\n\",\n        \"output\": \" Yes, GdAl7Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4CuNi5\\n\",\n        \"output\": \" No, Ti4CuNi5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf7(Fe27B4)3\\n\",\n        \"output\": \" Yes, Hf7(Fe27B4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr67Cu33\\n\",\n        \"output\": \" Yes, Zr67Cu33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe64Co19B17\\n\",\n        \"output\": \" Yes, Fe64Co19B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni73Mo7P20\\n\",\n        \"output\": \" Yes, Ni73Mo7P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu4Ni37P9\\n\",\n        \"output\": \" Yes, Cu4Ni37P9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co14B6C5\\n\",\n        \"output\": \" Yes, Co14B6C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd30Fe51.5B18.5\\n\",\n        \"output\": \" Yes, Nd30Fe51.5B18.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti34.4Nb20Cu45.6\\n\",\n        \"output\": \" Yes, Ti34.4Nb20Cu45.6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti13Si3Ni4\\n\",\n        \"output\": \" Yes, Ti13Si3Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiNi7P2\\n\",\n        \"output\": \" Yes, TiNi7P2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" B8Mo55.5Ru36.5\\n\",\n        \"output\": \" Yes, B8Mo55.5Ru36.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd(Al5Ni)4\\n\",\n        \"output\": \" Yes, Nd(Al5Ni)4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co17SiB2\\n\",\n        \"output\": \" No, Co17SiB2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3Ni16C\\n\",\n        \"output\": \" No, Si3Ni16C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V5Fe43B2\\n\",\n        \"output\": \" No, V5Fe43B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr7Fe9B4\\n\",\n        \"output\": \" Yes, Cr7Fe9B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn4Al13Si3\\n\",\n        \"output\": \" No, Mn4Al13Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg7Ni2\\n\",\n        \"output\": \" Yes, YMg7Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni33B17\\n\",\n        \"output\": \" Yes, Ni33B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu4Si16.5Pd79.5\\n\",\n        \"output\": \" Yes, Cu4Si16.5Pd79.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe71.5Co11.5B17\\n\",\n        \"output\": \" Yes, Fe71.5Co11.5B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe85NiB14\\n\",\n        \"output\": \" Yes, Fe85NiB14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni9P5Pt6\\n\",\n        \"output\": \" Yes, Ni9P5Pt6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La12Ni13\\n\",\n        \"output\": \" Yes, La12Ni13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co29(W4C3)3\\n\",\n        \"output\": \" No, Co29(W4C3)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd5Al37Ni8\\n\",\n        \"output\": \" Yes, Nd5Al37Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd(Al28Ni5)3\\n\",\n        \"output\": \" Yes, Nd(Al28Ni5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5Mg4Ni\\n\",\n        \"output\": \" No, Nd5Mg4Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf6Cu3Ni\\n\",\n        \"output\": \" Yes, Hf6Cu3Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11AlNi8\\n\",\n        \"output\": \" Yes, Zr11AlNi8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co10Ni73P17\\n\",\n        \"output\": \" No, Co10Ni73P17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2V2Co21\\n\",\n        \"output\": \" Yes, Zr2V2Co21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La9Al22Ni19\\n\",\n        \"output\": \" Yes, La9Al22Ni19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaAl4\\n\",\n        \"output\": \" No, LaAl4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Fe85B8\\n\",\n        \"output\": \" Yes, Zr7Fe85B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2Al41Ni7\\n\",\n        \"output\": \" Yes, Zr2Al41Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Si3Ni5\\n\",\n        \"output\": \" No, Ti2Si3Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf22.8Zr53.2Fe24\\n\",\n        \"output\": \" Yes, Hf22.8Zr53.2Fe24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr28.8Nb33Cu38.2\\n\",\n        \"output\": \" Yes, Zr28.8Nb33Cu38.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf32.3Nb25Cu42.7\\n\",\n        \"output\": \" Yes, Hf32.3Nb25Cu42.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co29Mo10C11\\n\",\n        \"output\": \" Yes, Co29Mo10C11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe82P11.5C6.5\\n\",\n        \"output\": \" Yes, Fe82P11.5C6.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Co37B8\\n\",\n        \"output\": \" Yes, Zr5Co37B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Mn17Co\\n\",\n        \"output\": \" Yes, Zr2Mn17Co has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl38Ni11\\n\",\n        \"output\": \" Yes, LaAl38Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu12.5Si16.5Pd71\\n\",\n        \"output\": \" Yes, Cu12.5Si16.5Pd71 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2(Mg5Ni)3\\n\",\n        \"output\": \" Yes, Nd2(Mg5Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd4Ni\\n\",\n        \"output\": \" No, Nd4Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf76(V3Si5)3\\n\",\n        \"output\": \" Yes, Hf76(V3Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" carnation\\n\",\n        \"output\": \" carnation is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sr11La52Cu37\\n\",\n        \"output\": \" Yes, Sr11La52Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al17V\\n\",\n        \"output\": \" No, Ce2Al17V does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe13Ag12\\n\",\n        \"output\": \" No, Fe13Ag12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr5(Fe14B)3\\n\",\n        \"output\": \" Yes, Cr5(Fe14B)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni29(Mo4C3)3\\n\",\n        \"output\": \" No, Ni29(Mo4C3)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Al15Ni2\\n\",\n        \"output\": \" No, La3Al15Ni2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Al85Ni13\\n\",\n        \"output\": \" Yes, Nd2Al85Ni13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" buffet\\n\",\n        \"output\": \" buffet is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4(Co6Mo)3\\n\",\n        \"output\": \" Yes, Zr4(Co6Mo)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13AlCu6\\n\",\n        \"output\": \" Yes, Zr13AlCu6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La63Cu37\\n\",\n        \"output\": \" Yes, La63Cu37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr17Al59Ni24\\n\",\n        \"output\": \" Yes, Zr17Al59Ni24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca9La57.5Cu33.5\\n\",\n        \"output\": \" Yes, Ca9La57.5Cu33.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf82(VSi5)3\\n\",\n        \"output\": \" Yes, Hf82(VSi5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La83Al3Ni14\\n\",\n        \"output\": \" Yes, La83Al3Ni14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al83Fe3Ni14\\n\",\n        \"output\": \" No, Al83Fe3Ni14 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr3La70Cu27\\n\",\n        \"output\": \" Yes, Sr3La70Cu27 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Pd80Au3.5\\n\",\n        \"output\": \" Yes, Si16.5Pd80Au3.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu3Ni80B17\\n\",\n        \"output\": \" Yes, Cu3Ni80B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al22Co2Ni\\n\",\n        \"output\": \" No, Al22Co2Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe38.5Ni38.5B23\\n\",\n        \"output\": \" Yes, Fe38.5Ni38.5B23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Fe82B11\\n\",\n        \"output\": \" Yes, Ti7Fe82B11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu2Ni37P11\\n\",\n        \"output\": \" Yes, Cu2Ni37P11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2.5Mg97.5\\n\",\n        \"output\": \" No, Nd2.5Mg97.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6VGe3\\n\",\n        \"output\": \" Yes, Al6VGe3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe78B17C5\\n\",\n        \"output\": \" Yes, Fe78B17C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl41Ni8\\n\",\n        \"output\": \" Yes, NdAl41Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" cable\\n\",\n        \"output\": \" cable is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg6Al3Zn\\n\",\n        \"output\": \" No, Mg6Al3Zn does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr35Fe14Pd\\n\",\n        \"output\": \" Yes, Zr35Fe14Pd has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al43Fe2Ni5\\n\",\n        \"output\": \" No, Al43Fe2Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl18Ni\\n\",\n        \"output\": \" No, CeAl18Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr67Co28P5\\n\",\n        \"output\": \" Yes, Zr67Co28P5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TaNb15Si4\\n\",\n        \"output\": \" Yes, TaNb15Si4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb40Si7C3\\n\",\n        \"output\": \" Yes, Nb40Si7C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Al13Ni4\\n\",\n        \"output\": \" Yes, Nd3Al13Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu52.8Ni27.2P20\\n\",\n        \"output\": \" Yes, Cu52.8Ni27.2P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al26V5Ge19\\n\",\n        \"output\": \" Yes, Al26V5Ge19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe20B2P3\\n\",\n        \"output\": \" Yes, Fe20B2P3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co22B2C\\n\",\n        \"output\": \" No, Co22B2C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb11Si4Mo5\\n\",\n        \"output\": \" Yes, Nb11Si4Mo5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15Al2Ni3\\n\",\n        \"output\": \" Yes, Zr15Al2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe38Cu5B7\\n\",\n        \"output\": \" No, Fe38Cu5B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg9Mn\\n\",\n        \"output\": \" No, Mg9Mn does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co15Si2C3\\n\",\n        \"output\": \" No, Co15Si2C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al6Fe39B5\\n\",\n        \"output\": \" No, Al6Fe39B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu(Ni5P)4\\n\",\n        \"output\": \" No, Cu(Ni5P)4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd4Al13Ni3\\n\",\n        \"output\": \" No, Nd4Al13Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn21Co17B12\\n\",\n        \"output\": \" Yes, Mn21Co17B12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe72.5P15C12.5\\n\",\n        \"output\": \" Yes, Fe72.5P15C12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ta3Nb5Ni12\\n\",\n        \"output\": \" Yes, Ta3Nb5Ni12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr25Fe57.5B17.5\\n\",\n        \"output\": \" Yes, Cr25Fe57.5B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SiNi15C4\\n\",\n        \"output\": \" No, SiNi15C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni13B12\\n\",\n        \"output\": \" No, Ni13B12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Pd81.5Au2\\n\",\n        \"output\": \" Yes, Si16.5Pd81.5Au2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al43FeCo6\\n\",\n        \"output\": \" Yes, Al43FeCo6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Al4Ni9\\n\",\n        \"output\": \" Yes, Zr7Al4Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al11Cr2Si7\\n\",\n        \"output\": \" Yes, Al11Cr2Si7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al47Fe2Ni\\n\",\n        \"output\": \" No, Al47Fe2Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn(Al7Ni)3\\n\",\n        \"output\": \" No, Mn(Al7Ni)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Al47\\n\",\n        \"output\": \" No, Nd3Al47 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al57Co18Ge25\\n\",\n        \"output\": \" Yes, Al57Co18Ge25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La2AlCu7\\n\",\n        \"output\": \" No, La2AlCu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Pd76.8Au6.7\\n\",\n        \"output\": \" Yes, Si16.5Pd76.8Au6.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co75W12.5C12.5\\n\",\n        \"output\": \" No, Co75W12.5C12.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr41Ni9\\n\",\n        \"output\": \" Yes, Zr41Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr72Ti23Si5\\n\",\n        \"output\": \" Yes, Zr72Ti23Si5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu61.6Ni18.4P20\\n\",\n        \"output\": \" Yes, Cu61.6Ni18.4P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca7.5Mg82.5Zn10\\n\",\n        \"output\": \" No, Ca7.5Mg82.5Zn10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Pd79.5Au4\\n\",\n        \"output\": \" Yes, Si16.5Pd79.5Au4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43Fe4Ni3\\n\",\n        \"output\": \" No, Al43Fe4Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe41B5Mo4\\n\",\n        \"output\": \" Yes, Fe41B5Mo4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr31(Ti3Si20)3\\n\",\n        \"output\": \" Yes, Zr31(Ti3Si20)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrCu4\\n\",\n        \"output\": \" No, ZrCu4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrBe\\n\",\n        \"output\": \" Yes, ZrBe has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CoNi38P11\\n\",\n        \"output\": \" No, CoNi38P11 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" GdAl\\n\",\n        \"output\": \" Yes, GdAl has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3AlCu6\\n\",\n        \"output\": \" Yes, Ti3AlCu6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe40B9Pd\\n\",\n        \"output\": \" Yes, Fe40B9Pd has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al6Co27B17\\n\",\n        \"output\": \" Yes, Al6Co27B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Al47Co\\n\",\n        \"output\": \" No, Ce2Al47Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" china\\n\",\n        \"output\": \" china is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co71B29\\n\",\n        \"output\": \" Yes, Co71B29 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe8BC\\n\",\n        \"output\": \" Yes, Fe8BC has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Ti3Cu10\\n\",\n        \"output\": \" Yes, Zr7Ti3Cu10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiAl10Cu9\\n\",\n        \"output\": \" Yes, TiAl10Cu9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr74Fe9P17\\n\",\n        \"output\": \" Yes, Cr74Fe9P17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf71V14Si15\\n\",\n        \"output\": \" Yes, Hf71V14Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb6Fe41B3\\n\",\n        \"output\": \" Yes, Nb6Fe41B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr0.5Si20Pd79.5\\n\",\n        \"output\": \" Yes, Cr0.5Si20Pd79.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al10Co23B17\\n\",\n        \"output\": \" Yes, Al10Co23B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al39Co5Ge6\\n\",\n        \"output\": \" Yes, Al39Co5Ge6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7V2Ni11\\n\",\n        \"output\": \" Yes, Zr7V2Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4Fe41B5\\n\",\n        \"output\": \" Yes, Zr4Fe41B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti2Al3\\n\",\n        \"output\": \" No, Ti2Al3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co7MoC2\\n\",\n        \"output\": \" Yes, Co7MoC2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti59Be41\\n\",\n        \"output\": \" Yes, Ti59Be41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn4Al83Ni13\\n\",\n        \"output\": \" No, Mn4Al83Ni13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37B7Mo6\\n\",\n        \"output\": \" Yes, Fe37B7Mo6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al88CoNi11\\n\",\n        \"output\": \" No, Al88CoNi11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83B6P11\\n\",\n        \"output\": \" Yes, Fe83B6P11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co16(B2C)3\\n\",\n        \"output\": \" Yes, Co16(B2C)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CaAl18Ni\\n\",\n        \"output\": \" No, CaAl18Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Al42Ni5\\n\",\n        \"output\": \" Yes, Zr3Al42Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Al5Ni2\\n\",\n        \"output\": \" Yes, La3Al5Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe73Ni10B17\\n\",\n        \"output\": \" Yes, Fe73Ni10B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si7.5Ni75B17.5\\n\",\n        \"output\": \" Yes, Si7.5Ni75B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn5Fe41B4\\n\",\n        \"output\": \" No, Mn5Fe41B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9AlNi10\\n\",\n        \"output\": \" Yes, Zr9AlNi10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al86.7Fe1Ni12.3\\n\",\n        \"output\": \" Yes, Al86.7Fe1Ni12.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4(CuNi)3\\n\",\n        \"output\": \" Yes, Ti4(CuNi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce5Al83Co12\\n\",\n        \"output\": \" Yes, Ce5Al83Co12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe58Co25B17\\n\",\n        \"output\": \" Yes, Fe58Co25B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti11Al9\\n\",\n        \"output\": \" No, Ti11Al9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co3B2\\n\",\n        \"output\": \" Yes, Co3B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si7Ni76B17\\n\",\n        \"output\": \" Yes, Si7Ni76B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta(NbNi2)3\\n\",\n        \"output\": \" Yes, Ta(NbNi2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co1.7Si16.5Pd81.8\\n\",\n        \"output\": \" Yes, Co1.7Si16.5Pd81.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al10Fe33B7\\n\",\n        \"output\": \" Yes, Al10Fe33B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" NdAl17Ni2\\n\",\n        \"output\": \" Yes, NdAl17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce(Al2Ni)3\\n\",\n        \"output\": \" Yes, Ce(Al2Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe36B5Mo9\\n\",\n        \"output\": \" Yes, Fe36B5Mo9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm2Al23\\n\",\n        \"output\": \" Yes, Sm2Al23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y13Al82Ni5\\n\",\n        \"output\": \" Yes, Y13Al82Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti5(AlCu4)3\\n\",\n        \"output\": \" Yes, Ti5(AlCu4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni81.5B14.8P3.7\\n\",\n        \"output\": \" Yes, Ni81.5B14.8P3.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co67.5Si22.5C10\\n\",\n        \"output\": \" Yes, Co67.5Si22.5C10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y9Al85Cu6\\n\",\n        \"output\": \" Yes, Y9Al85Cu6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5.2Co86.8W8\\n\",\n        \"output\": \" Yes, Zr5.2Co86.8W8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd7Mg2Ni\\n\",\n        \"output\": \" No, Nd7Mg2Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe15CoB4\\n\",\n        \"output\": \" Yes, Fe15CoB4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti15Be4Si\\n\",\n        \"output\": \" No, Ti15Be4Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe35(Mo2C3)3\\n\",\n        \"output\": \" Yes, Fe35(Mo2C3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SmAl18Ni\\n\",\n        \"output\": \" Yes, SmAl18Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe75Mo17C8\\n\",\n        \"output\": \" Yes, Fe75Mo17C8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Fe93\\n\",\n        \"output\": \" No, Zr7Fe93 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe17B2C\\n\",\n        \"output\": \" Yes, Fe17B2C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" window\\n\",\n        \"output\": \" window is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf62Nb23Si15\\n\",\n        \"output\": \" Yes, Hf62Nb23Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11(Nb2Si)3\\n\",\n        \"output\": \" Yes, Zr11(Nb2Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79(Ni5B2)3\\n\",\n        \"output\": \" No, Fe79(Ni5B2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd11Fe89\\n\",\n        \"output\": \" Yes, Nd11Fe89 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd15Fe82B3\\n\",\n        \"output\": \" Yes, Nd15Fe82B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr47Nb40Si13\\n\",\n        \"output\": \" Yes, Zr47Nb40Si13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Al7Ni\\n\",\n        \"output\": \" No, Nd2Al7Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al71Co4Si25\\n\",\n        \"output\": \" Yes, Al71Co4Si25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf3Ta2Fe5\\n\",\n        \"output\": \" Yes, Hf3Ta2Fe5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr56.95Cu15Ni28.05\\n\",\n        \"output\": \" Yes, Zr56.95Cu15Ni28.05 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13(Al2Ni)4\\n\",\n        \"output\": \" Yes, Zr13(Al2Ni)4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr17(Ni3P)2\\n\",\n        \"output\": \" Yes, Zr17(Ni3P)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni81.5P18.5\\n\",\n        \"output\": \" Yes, Ni81.5P18.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8AlNi\\n\",\n        \"output\": \" Yes, Zr8AlNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe67(Cu5B6)3\\n\",\n        \"output\": \" No, Fe67(Cu5B6)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2CuNi2\\n\",\n        \"output\": \" No, Ti2CuNi2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3(Ni9B2)2\\n\",\n        \"output\": \" Yes, Si3(Ni9B2)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg5Al74Pd21\\n\",\n        \"output\": \" No, Mg5Al74Pd21 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al43Fe2Co5\\n\",\n        \"output\": \" No, Al43Fe2Co5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La(AlCu)2\\n\",\n        \"output\": \" No, La(AlCu)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe69B16Mo15\\n\",\n        \"output\": \" Yes, Fe69B16Mo15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg70(Cu9Au)3\\n\",\n        \"output\": \" Yes, Mg70(Cu9Au)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B16C3\\n\",\n        \"output\": \" Yes, Fe81B16C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl\\n\",\n        \"output\": \" Yes, LaAl has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La2Mg13Ni5\\n\",\n        \"output\": \" Yes, La2Mg13Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti1.1Al98.9\\n\",\n        \"output\": \" No, Ti1.1Al98.9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn40.5Co43.5B16\\n\",\n        \"output\": \" Yes, Mn40.5Co43.5B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce4Mg11Cu5\\n\",\n        \"output\": \" No, Ce4Mg11Cu5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr24.5Fe56B19.5\\n\",\n        \"output\": \" Yes, Cr24.5Fe56B19.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn51Co33B16\\n\",\n        \"output\": \" Yes, Mn51Co33B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr75SiNi24\\n\",\n        \"output\": \" Yes, Zr75SiNi24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe81B12Mo7\\n\",\n        \"output\": \" Yes, Fe81B12Mo7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr17Al2Ni\\n\",\n        \"output\": \" No, Zr17Al2Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La6AlNi3\\n\",\n        \"output\": \" Yes, La6AlNi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni24B21C5\\n\",\n        \"output\": \" Yes, Ni24B21C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Nb15Co83\\n\",\n        \"output\": \" Yes, Mn2Nb15Co83 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe8PC\\n\",\n        \"output\": \" Yes, Fe8PC has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ta7Ni13\\n\",\n        \"output\": \" Yes, Ta7Ni13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4Al41Ni5\\n\",\n        \"output\": \" No, Zr4Al41Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti61Be39\\n\",\n        \"output\": \" Yes, Ti61Be39 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm3Al15Ni2\\n\",\n        \"output\": \" Yes, Sm3Al15Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Al5Cu3\\n\",\n        \"output\": \" No, Ti2Al5Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl3Ni\\n\",\n        \"output\": \" No, CeAl3Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7.5Cr4Co88.5\\n\",\n        \"output\": \" Yes, Zr7.5Cr4Co88.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn43(Co11B8)3\\n\",\n        \"output\": \" Yes, Mn43(Co11B8)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti13Ni7\\n\",\n        \"output\": \" Yes, Ti13Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Al2Cu21\\n\",\n        \"output\": \" Yes, Nd2Al2Cu21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al24Co\\n\",\n        \"output\": \" No, Al24Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Fe3\\n\",\n        \"output\": \" Yes, Zr7Fe3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf58(Nb9Si5)3\\n\",\n        \"output\": \" Yes, Hf58(Nb9Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr67Ni33\\n\",\n        \"output\": \" Yes, Zr67Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn2Al23\\n\",\n        \"output\": \" No, Mn2Al23 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CrNi7P2\\n\",\n        \"output\": \" Yes, CrNi7P2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn7Fe33B10\\n\",\n        \"output\": \" Yes, Mn7Fe33B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7.1Fe83.4B9.5\\n\",\n        \"output\": \" No, Nb7.1Fe83.4B9.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaCu\\n\",\n        \"output\": \" No, LaCu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Ni13\\n\",\n        \"output\": \" Yes, Zr7Ni13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co12.5Si16.5Pd71\\n\",\n        \"output\": \" Yes, Co12.5Si16.5Pd71 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5TiSi44\\n\",\n        \"output\": \" No, Zr5TiSi44 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La4AlCu5\\n\",\n        \"output\": \" No, La4AlCu5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La62.5Cu37.5\\n\",\n        \"output\": \" Yes, La62.5Cu37.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co21B4\\n\",\n        \"output\": \" Yes, Co21B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2Al3Ni5\\n\",\n        \"output\": \" Yes, La2Al3Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" SiNi15B4\\n\",\n        \"output\": \" Yes, SiNi15B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3(Ni8B3)2\\n\",\n        \"output\": \" No, Si3(Ni8B3)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb15Fe79B6\\n\",\n        \"output\": \" No, Nb15Fe79B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37Si5B8\\n\",\n        \"output\": \" Yes, Fe37Si5B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Al87Ni10\\n\",\n        \"output\": \" Yes, Y3Al87Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" airplane\\n\",\n        \"output\": \" airplane is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb40Ni59Ir\\n\",\n        \"output\": \" Yes, Nb40Ni59Ir has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al6Ni31B13\\n\",\n        \"output\": \" Yes, Al6Ni31B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti7Si2Ni\\n\",\n        \"output\": \" No, Ti7Si2Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe39Ni10B\\n\",\n        \"output\": \" No, Fe39Ni10B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe69Ni25B6\\n\",\n        \"output\": \" No, Fe69Ni25B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2AlNi\\n\",\n        \"output\": \" Yes, La2AlNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11(Ta2Si)3\\n\",\n        \"output\": \" Yes, Zr11(Ta2Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Nb2Al15\\n\",\n        \"output\": \" No, Ce3Nb2Al15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti15Si2Ni3\\n\",\n        \"output\": \" Yes, Ti15Si2Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr60.3V10Ni29.7\\n\",\n        \"output\": \" Yes, Zr60.3V10Ni29.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al8Fe29B13\\n\",\n        \"output\": \" Yes, Al8Fe29B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe39BMo10\\n\",\n        \"output\": \" No, Fe39BMo10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf47Nb38Si15\\n\",\n        \"output\": \" Yes, Hf47Nb38Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeAl44Co5\\n\",\n        \"output\": \" Yes, CeAl44Co5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" mayonnaise\\n\",\n        \"output\": \" mayonnaise is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.95Fe33Ni0.05\\n\",\n        \"output\": \" Yes, Zr66.95Fe33Ni0.05 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe8BMo\\n\",\n        \"output\": \" Yes, Fe8BMo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co33W8C9\\n\",\n        \"output\": \" No, Co33W8C9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl44Ni5\\n\",\n        \"output\": \" Yes, LaAl44Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg9Cu\\n\",\n        \"output\": \" No, Mg9Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd9Al85Ni6\\n\",\n        \"output\": \" Yes, Gd9Al85Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co15SiC4\\n\",\n        \"output\": \" No, Co15SiC4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu10Si17Pd73\\n\",\n        \"output\": \" Yes, Cu10Si17Pd73 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg7Zn3\\n\",\n        \"output\": \" Yes, Mg7Zn3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8Ni31B11\\n\",\n        \"output\": \" Yes, Al8Ni31B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe81B12W7\\n\",\n        \"output\": \" Yes, Fe81B12W7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Al16Ni25\\n\",\n        \"output\": \" Yes, La9Al16Ni25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CrFe15B4\\n\",\n        \"output\": \" Yes, CrFe15B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe10B19N21\\n\",\n        \"output\": \" Yes, Fe10B19N21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5B20W2.5\\n\",\n        \"output\": \" Yes, Fe77.5B20W2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al12V3Cu5\\n\",\n        \"output\": \" No, Al12V3Cu5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81Ni5B14\\n\",\n        \"output\": \" Yes, Fe81Ni5B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10.4Cr10.6Co79\\n\",\n        \"output\": \" Yes, Zr10.4Cr10.6Co79 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Fe86B9\\n\",\n        \"output\": \" Yes, Zr5Fe86B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" rhinoceros\\n\",\n        \"output\": \" rhinoceros is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" seeder\\n\",\n        \"output\": \" seeder is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb9.3Fe77.5B13.2\\n\",\n        \"output\": \" Yes, Nb9.3Fe77.5B13.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Al12Ni5\\n\",\n        \"output\": \" Yes, Y3Al12Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sm7Al43\\n\",\n        \"output\": \" Yes, Sm7Al43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni75B13C12\\n\",\n        \"output\": \" No, Ni75B13C12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Al5Cu42\\n\",\n        \"output\": \" No, Ce3Al5Cu42 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti19Si\\n\",\n        \"output\": \" No, Ti19Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" racing\\n\",\n        \"output\": \" racing is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf79(V2Si5)3\\n\",\n        \"output\": \" Yes, Hf79(V2Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2(Co13B3)3\\n\",\n        \"output\": \" Yes, Ti2(Co13B3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni81.5B12P6.5\\n\",\n        \"output\": \" Yes, Ni81.5B12P6.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrCo8B\\n\",\n        \"output\": \" Yes, ZrCo8B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce9Al91\\n\",\n        \"output\": \" Yes, Ce9Al91 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al10Fe31B9\\n\",\n        \"output\": \" Yes, Al10Fe31B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti5Co17B3\\n\",\n        \"output\": \" Yes, Ti5Co17B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg12Cu5\\n\",\n        \"output\": \" Yes, Nd3Mg12Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb16.5Ni66.5B17\\n\",\n        \"output\": \" Yes, Nb16.5Ni66.5B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeMg15Ni4\\n\",\n        \"output\": \" Yes, CeMg15Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co14B9C2\\n\",\n        \"output\": \" No, Co14B9C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al77V3Cu20\\n\",\n        \"output\": \" No, Al77V3Cu20 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7Al5Ni13\\n\",\n        \"output\": \" Yes, Zr7Al5Ni13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79B20Mo\\n\",\n        \"output\": \" Yes, Fe79B20Mo has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAl24\\n\",\n        \"output\": \" No, MnAl24 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2VCo22\\n\",\n        \"output\": \" Yes, Zr2VCo22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5B22.5\\n\",\n        \"output\": \" Yes, Fe77.5B22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf5Cu2Ni3\\n\",\n        \"output\": \" Yes, Hf5Cu2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg75Zn22\\n\",\n        \"output\": \" Yes, La3Mg75Zn22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ba2La59Cu39\\n\",\n        \"output\": \" Yes, Ba2La59Cu39 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce5Al91Ni4\\n\",\n        \"output\": \" Yes, Ce5Al91Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn8Nb15Co77\\n\",\n        \"output\": \" Yes, Mn8Nb15Co77 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y20Mg79Cu\\n\",\n        \"output\": \" No, Y20Mg79Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9Al30Ni11\\n\",\n        \"output\": \" Yes, Zr9Al30Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7(Cr6Co25)3\\n\",\n        \"output\": \" Yes, Zr7(Cr6Co25)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15V2Si3\\n\",\n        \"output\": \" Yes, Zr15V2Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg3Ni\\n\",\n        \"output\": \" Yes, YMg3Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe82.5P7.5C10\\n\",\n        \"output\": \" No, Fe82.5P7.5C10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2Mg17Ni\\n\",\n        \"output\": \" No, La2Mg17Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe13Si5C2\\n\",\n        \"output\": \" Yes, Fe13Si5C2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La6Al3Ni\\n\",\n        \"output\": \" Yes, La6Al3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe41(W2C)3\\n\",\n        \"output\": \" No, Fe41(W2C)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu5Ni34P11\\n\",\n        \"output\": \" Yes, Cu5Ni34P11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co3BC\\n\",\n        \"output\": \" Yes, Co3BC has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg9Al26Pd15\\n\",\n        \"output\": \" No, Mg9Al26Pd15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe72.5Si10B17.5\\n\",\n        \"output\": \" Yes, Fe72.5Si10B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti20P19Pd61\\n\",\n        \"output\": \" Yes, Ti20P19Pd61 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe79W16C5\\n\",\n        \"output\": \" No, Fe79W16C5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaAl17Cu2\\n\",\n        \"output\": \" No, LaAl17Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe8CuB\\n\",\n        \"output\": \" No, Fe8CuB does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CaMg7Al2\\n\",\n        \"output\": \" Yes, CaMg7Al2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al49Co10Si41\\n\",\n        \"output\": \" Yes, Al49Co10Si41 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd20Fe61.5B18.5\\n\",\n        \"output\": \" Yes, Nd20Fe61.5B18.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr23V30Ni47\\n\",\n        \"output\": \" Yes, Zr23V30Ni47 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti17VSi2\\n\",\n        \"output\": \" No, Ti17VSi2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La4Mg7Ni9\\n\",\n        \"output\": \" Yes, La4Mg7Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y(MgCu)2\\n\",\n        \"output\": \" Yes, Y(MgCu)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Co19B4\\n\",\n        \"output\": \" Yes, Mn2Co19B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co3Si\\n\",\n        \"output\": \" No, Co3Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb17Si3\\n\",\n        \"output\": \" Yes, Nb17Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni28B17C5\\n\",\n        \"output\": \" Yes, Ni28B17C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Al14Cu3\\n\",\n        \"output\": \" No, Ce3Al14Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr7Fe41B2\\n\",\n        \"output\": \" No, Cr7Fe41B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La9Al7Ni4\\n\",\n        \"output\": \" Yes, La9Al7Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co15WC4\\n\",\n        \"output\": \" No, Co15WC4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe2CuAg\\n\",\n        \"output\": \" No, Fe2CuAg does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf4TaFe5\\n\",\n        \"output\": \" Yes, Hf4TaFe5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe48Ni35B17\\n\",\n        \"output\": \" Yes, Fe48Ni35B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb15Fe26Co59\\n\",\n        \"output\": \" Yes, Nb15Fe26Co59 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr15Fe81B4\\n\",\n        \"output\": \" No, Cr15Fe81B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13Si3Mo4\\n\",\n        \"output\": \" Yes, Zr13Si3Mo4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al62Ni13Ge25\\n\",\n        \"output\": \" Yes, Al62Ni13Ge25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SiNi9\\n\",\n        \"output\": \" No, SiNi9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnFe8B\\n\",\n        \"output\": \" No, MnFe8B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr67.5Cu25B7.5\\n\",\n        \"output\": \" Yes, Zr67.5Cu25B7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co87.5W2.5C10\\n\",\n        \"output\": \" No, Co87.5W2.5C10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al35Fe8Ni7\\n\",\n        \"output\": \" Yes, Al35Fe8Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La11Al2Ni7\\n\",\n        \"output\": \" Yes, La11Al2Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15.2V12Co72.8\\n\",\n        \"output\": \" Yes, Zr15.2V12Co72.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Al4Ni7\\n\",\n        \"output\": \" Yes, La9Al4Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf10V7Si3\\n\",\n        \"output\": \" Yes, Hf10V7Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" stage\\n\",\n        \"output\": \" stage is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe40B3P7\\n\",\n        \"output\": \" Yes, Fe40B3P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe19(BMo)3\\n\",\n        \"output\": \" Yes, Fe19(BMo)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ag8.5Pd75\\n\",\n        \"output\": \" Yes, Si16.5Ag8.5Pd75 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf13Al2Cu5\\n\",\n        \"output\": \" Yes, Hf13Al2Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr15La48Cu37\\n\",\n        \"output\": \" Yes, Sr15La48Cu37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr79Cu20B\\n\",\n        \"output\": \" No, Zr79Cu20B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr(Fe2Co)3\\n\",\n        \"output\": \" Yes, Zr(Fe2Co)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" surgeon\\n\",\n        \"output\": \" surgeon is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf3CuNi\\n\",\n        \"output\": \" Yes, Hf3CuNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al4Fe41B5\\n\",\n        \"output\": \" No, Al4Fe41B5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al14(SiNi)3\\n\",\n        \"output\": \" Yes, Al14(SiNi)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La8(Al3Ni)3\\n\",\n        \"output\": \" Yes, La8(Al3Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti12Si3Ni5\\n\",\n        \"output\": \" Yes, Ti12Si3Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu10Si15.8Pd74.2\\n\",\n        \"output\": \" Yes, Cu10Si15.8Pd74.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrFe9\\n\",\n        \"output\": \" Yes, ZrFe9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co13SiB6\\n\",\n        \"output\": \" Yes, Co13SiB6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce6Al87Ni7\\n\",\n        \"output\": \" Yes, Ce6Al87Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd3Al13Ni4\\n\",\n        \"output\": \" Yes, Gd3Al13Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2Mg17Ni\\n\",\n        \"output\": \" Yes, Ce2Mg17Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni37B8C5\\n\",\n        \"output\": \" Yes, Ni37B8C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr17Si3\\n\",\n        \"output\": \" Yes, Zr17Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn3Fe87B10\\n\",\n        \"output\": \" No, Mn3Fe87B10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAl44Ni5\\n\",\n        \"output\": \" Yes, CeAl44Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La15Al3Ni2\\n\",\n        \"output\": \" Yes, La15Al3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al10Cr3Si7\\n\",\n        \"output\": \" Yes, Al10Cr3Si7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al47Co3\\n\",\n        \"output\": \" No, Al47Co3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5(Fe14B)3\\n\",\n        \"output\": \" Yes, Zr5(Fe14B)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Al4Ni3\\n\",\n        \"output\": \" Yes, Zr13Al4Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl17Cu2\\n\",\n        \"output\": \" Yes, CeAl17Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr13Fe33B4\\n\",\n        \"output\": \" No, Cr13Fe33B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co19(BC)3\\n\",\n        \"output\": \" Yes, Co19(BC)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn26.5Co49.5B24\\n\",\n        \"output\": \" Yes, Mn26.5Co49.5B24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn2Al43Co5\\n\",\n        \"output\": \" No, Mn2Al43Co5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co14Mo6C5\\n\",\n        \"output\": \" Yes, Co14Mo6C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce(Al6Fe)7\\n\",\n        \"output\": \" No, Ce(Al6Fe)7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2Mg7Cu\\n\",\n        \"output\": \" Yes, Y2Mg7Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd7Ni3\\n\",\n        \"output\": \" Yes, Nd7Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2Al95Co3\\n\",\n        \"output\": \" No, Ce2Al95Co3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb40Ni59Pt\\n\",\n        \"output\": \" Yes, Nb40Ni59Pt has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr39Ti26Si35\\n\",\n        \"output\": \" Yes, Zr39Ti26Si35 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16(Pd25Au3)3\\n\",\n        \"output\": \" Yes, Si16(Pd25Au3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si17Pd79Au4\\n\",\n        \"output\": \" Yes, Si17Pd79Au4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al91(Fe2Ni)3\\n\",\n        \"output\": \" No, Al91(Fe2Ni)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al21FeCo3\\n\",\n        \"output\": \" No, Al21FeCo3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" storm\\n\",\n        \"output\": \" storm is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13V2Ni5\\n\",\n        \"output\": \" Yes, Zr13V2Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe18Ni53B29\\n\",\n        \"output\": \" Yes, Fe18Ni53B29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti51Al15Cu34\\n\",\n        \"output\": \" Yes, Ti51Al15Cu34 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti15Nb27Si8\\n\",\n        \"output\": \" Yes, Ti15Nb27Si8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al12Ni25B13\\n\",\n        \"output\": \" Yes, Al12Ni25B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co17W5C3\\n\",\n        \"output\": \" No, Co17W5C3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg17Ti36Al47\\n\",\n        \"output\": \" No, Mg17Ti36Al47 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr13Fe34B3\\n\",\n        \"output\": \" No, Cr13Fe34B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ho2Fe19B4\\n\",\n        \"output\": \" Yes, Ho2Fe19B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si9Pd8Au33\\n\",\n        \"output\": \" Yes, Si9Pd8Au33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti41Al59\\n\",\n        \"output\": \" Yes, Ti41Al59 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11Ti5Si4\\n\",\n        \"output\": \" Yes, Zr11Ti5Si4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe43B2Mo5\\n\",\n        \"output\": \" No, Fe43B2Mo5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4Fe45B\\n\",\n        \"output\": \" Yes, Zr4Fe45B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaMg16Cu3\\n\",\n        \"output\": \" Yes, LaMg16Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al11(VGe2)3\\n\",\n        \"output\": \" Yes, Al11(VGe2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3B4Mo13\\n\",\n        \"output\": \" No, Si3B4Mo13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf2Ta3Fe5\\n\",\n        \"output\": \" Yes, Hf2Ta3Fe5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr47Ti8Si45\\n\",\n        \"output\": \" Yes, Zr47Ti8Si45 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al6Ni35B9\\n\",\n        \"output\": \" Yes, Al6Ni35B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CoSi2Pd7\\n\",\n        \"output\": \" Yes, CoSi2Pd7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe63Mo17C20\\n\",\n        \"output\": \" Yes, Fe63Mo17C20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" beauty\\n\",\n        \"output\": \" beauty is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" pasta\\n\",\n        \"output\": \" pasta is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2AlNi7\\n\",\n        \"output\": \" No, La2AlNi7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Ni73B17\\n\",\n        \"output\": \" Yes, Zr10Ni73B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg3Ti34Al63\\n\",\n        \"output\": \" Yes, Mg3Ti34Al63 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti15Co72.25B12.75\\n\",\n        \"output\": \" Yes, Ti15Co72.25B12.75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti7Be3\\n\",\n        \"output\": \" No, Ti7Be3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Fe17\\n\",\n        \"output\": \" Yes, Zr3Fe17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti8P19Pd73\\n\",\n        \"output\": \" Yes, Ti8P19Pd73 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti26(Nb5Si3)3\\n\",\n        \"output\": \" Yes, Ti26(Nb5Si3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg46Ti35Al19\\n\",\n        \"output\": \" No, Mg46Ti35Al19 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al86(FeNi)7\\n\",\n        \"output\": \" No, Al86(FeNi)7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb15Fe72.5Co12.5\\n\",\n        \"output\": \" Yes, Nb15Fe72.5Co12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La18Al65Ni17\\n\",\n        \"output\": \" Yes, La18Al65Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr62.5Be35Nb2.5\\n\",\n        \"output\": \" Yes, Zr62.5Be35Nb2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti4Al\\n\",\n        \"output\": \" No, Ti4Al does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" B3Mo7\\n\",\n        \"output\": \" No, B3Mo7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al2(Fe13B3)3\\n\",\n        \"output\": \" Yes, Al2(Fe13B3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Si3Ni8\\n\",\n        \"output\": \" Yes, Ti9Si3Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe74.9Si7.3B17.8\\n\",\n        \"output\": \" Yes, Fe74.9Si7.3B17.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si(BMo2)3\\n\",\n        \"output\": \" No, Si(BMo2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr10La61.5Cu28.5\\n\",\n        \"output\": \" Yes, Sr10La61.5Cu28.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe15Ni3B2\\n\",\n        \"output\": \" No, Fe15Ni3B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al4Co39B7\\n\",\n        \"output\": \" No, Al4Co39B7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr21Co18C11\\n\",\n        \"output\": \" Yes, Cr21Co18C11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Al4Cu7\\n\",\n        \"output\": \" Yes, Ti9Al4Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr14AlNi5\\n\",\n        \"output\": \" Yes, Zr14AlNi5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2AlNi\\n\",\n        \"output\": \" Yes, Ti2AlNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co17(WC)4\\n\",\n        \"output\": \" No, Co17(WC)4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr16Ni9\\n\",\n        \"output\": \" Yes, Zr16Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr7Fe34B9\\n\",\n        \"output\": \" Yes, Cr7Fe34B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiFe19B5\\n\",\n        \"output\": \" Yes, TiFe19B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al47Cr3\\n\",\n        \"output\": \" No, Al47Cr3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdMg4Cu5\\n\",\n        \"output\": \" Yes, NdMg4Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al86Fe3Ni11\\n\",\n        \"output\": \" Yes, Al86Fe3Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni18P5Pt2\\n\",\n        \"output\": \" No, Ni18P5Pt2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co85W7.5C7.5\\n\",\n        \"output\": \" No, Co85W7.5C7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La87Al11Ni2\\n\",\n        \"output\": \" Yes, La87Al11Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb5Fe83B12\\n\",\n        \"output\": \" Yes, Nb5Fe83B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B12C7\\n\",\n        \"output\": \" Yes, Fe81B12C7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr4Fe43B3\\n\",\n        \"output\": \" Yes, Cr4Fe43B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co33W10C7\\n\",\n        \"output\": \" No, Co33W10C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl17Ni2\\n\",\n        \"output\": \" Yes, LaAl17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf37Fe63\\n\",\n        \"output\": \" Yes, Hf37Fe63 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co6.7Si16.5Pd76.8\\n\",\n        \"output\": \" Yes, Co6.7Si16.5Pd76.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al15V3Cu2\\n\",\n        \"output\": \" No, Al15V3Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" hose\\n\",\n        \"output\": \" hose is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr19Ni62Mo19\\n\",\n        \"output\": \" Yes, Cr19Ni62Mo19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti58(Al5Ni)7\\n\",\n        \"output\": \" Yes, Ti58(Al5Ni)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg21Al53Pd26\\n\",\n        \"output\": \" Yes, Mg21Al53Pd26 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe6B9Mo85\\n\",\n        \"output\": \" Yes, Fe6B9Mo85 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3Ni40B7\\n\",\n        \"output\": \" No, Si3Ni40B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sm7(Al29Ni2)3\\n\",\n        \"output\": \" Yes, Sm7(Al29Ni2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe83B10C7\\n\",\n        \"output\": \" Yes, Fe83B10C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr13Co5Pd2\\n\",\n        \"output\": \" Yes, Zr13Co5Pd2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca2Al17Zn\\n\",\n        \"output\": \" Yes, Ca2Al17Zn has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb7(Fe27B4)3\\n\",\n        \"output\": \" Yes, Nb7(Fe27B4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4AlCu5\\n\",\n        \"output\": \" Yes, Ti4AlCu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr50.25Ti25Ni24.75\\n\",\n        \"output\": \" Yes, Zr50.25Ti25Ni24.75 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y3(Mg10Cu)2\\n\",\n        \"output\": \" Yes, Y3(Mg10Cu)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mo12P5Ru8\\n\",\n        \"output\": \" Yes, Mo12P5Ru8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti23Nb20Cu57\\n\",\n        \"output\": \" Yes, Ti23Nb20Cu57 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg30Ti43Al27\\n\",\n        \"output\": \" No, Mg30Ti43Al27 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Mg17Cu\\n\",\n        \"output\": \" Yes, Nd2Mg17Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe15Cu22Ag13\\n\",\n        \"output\": \" No, Fe15Cu22Ag13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr2(Fe5B)3\\n\",\n        \"output\": \" Yes, Cr2(Fe5B)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg16Mn3\\n\",\n        \"output\": \" No, YMg16Mn3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al86.5Ni11.5\\n\",\n        \"output\": \" Yes, Mn2Al86.5Ni11.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Fe89.946Si0.054\\n\",\n        \"output\": \" Yes, Zr10Fe89.946Si0.054 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe13Ni5B2\\n\",\n        \"output\": \" No, Fe13Ni5B2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr21Ti4Si25\\n\",\n        \"output\": \" Yes, Zr21Ti4Si25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe77Cu15B8\\n\",\n        \"output\": \" No, Fe77Cu15B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Al2Ni11\\n\",\n        \"output\": \" Yes, Zr7Al2Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2Al85Ni13\\n\",\n        \"output\": \" No, Mn2Al85Ni13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co62.5Si17.5B20\\n\",\n        \"output\": \" No, Co62.5Si17.5B20 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si2.5Ni72.5B25\\n\",\n        \"output\": \" No, Si2.5Ni72.5B25 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3(Mg10Ni)2\\n\",\n        \"output\": \" Yes, La3(Mg10Ni)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb7Co42B\\n\",\n        \"output\": \" Yes, Nb7Co42B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al90FeNi9\\n\",\n        \"output\": \" No, Al90FeNi9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe41Cu5B4\\n\",\n        \"output\": \" No, Fe41Cu5B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaMg14Zn5\\n\",\n        \"output\": \" Yes, LaMg14Zn5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni17B5C3\\n\",\n        \"output\": \" Yes, Ni17B5C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Cr4Fe41\\n\",\n        \"output\": \" Yes, Zr5Cr4Fe41 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" objective\\n\",\n        \"output\": \" objective is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf2CuNi\\n\",\n        \"output\": \" Yes, Hf2CuNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr12.5Co74.5Mo13\\n\",\n        \"output\": \" Yes, Zr12.5Co74.5Mo13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80Co3B17\\n\",\n        \"output\": \" Yes, Fe80Co3B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4(AlCu)3\\n\",\n        \"output\": \" No, Ti4(AlCu)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13V4Si3\\n\",\n        \"output\": \" Yes, Zr13V4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al6CrGe3\\n\",\n        \"output\": \" Yes, Al6CrGe3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe75Si12B13\\n\",\n        \"output\": \" Yes, Fe75Si12B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr37.5Cu55B7.5\\n\",\n        \"output\": \" Yes, Zr37.5Cu55B7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe91B7F2\\n\",\n        \"output\": \" No, Fe91B7F2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn5Fe87B8\\n\",\n        \"output\": \" No, Mn5Fe87B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83.5Cu0.5B16\\n\",\n        \"output\": \" Yes, Fe83.5Cu0.5B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd11.8Fe82.1B6.1\\n\",\n        \"output\": \" Yes, Nd11.8Fe82.1B6.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg5Al3Zn2\\n\",\n        \"output\": \" No, Mg5Al3Zn2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al8Co25B17\\n\",\n        \"output\": \" Yes, Al8Co25B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf2CuNi2\\n\",\n        \"output\": \" Yes, Hf2CuNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr28(Nb5Cu19)3\\n\",\n        \"output\": \" Yes, Zr28(Nb5Cu19)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn(Fe31B2)3\\n\",\n        \"output\": \" No, Mn(Fe31B2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn5(Al7Ge8)3\\n\",\n        \"output\": \" Yes, Mn5(Al7Ge8)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13Ta4Si3\\n\",\n        \"output\": \" Yes, Zr13Ta4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co67.5Si15C17.5\\n\",\n        \"output\": \" Yes, Co67.5Si15C17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg12Ti7Al\\n\",\n        \"output\": \" No, Mg12Ti7Al does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe43W2C5\\n\",\n        \"output\": \" No, Fe43W2C5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe79(B2Mo5)3\\n\",\n        \"output\": \" No, Fe79(B2Mo5)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si3Ni15C2\\n\",\n        \"output\": \" No, Si3Ni15C2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al89FeNi10\\n\",\n        \"output\": \" No, Al89FeNi10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti21Al15Ni14\\n\",\n        \"output\": \" Yes, Ti21Al15Ni14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La8Mg67Zn25\\n\",\n        \"output\": \" Yes, La8Mg67Zn25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Co44Mo3\\n\",\n        \"output\": \" Yes, Zr3Co44Mo3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr52.5Cu45B2.5\\n\",\n        \"output\": \" Yes, Zr52.5Cu45B2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe15P2C3\\n\",\n        \"output\": \" Yes, Fe15P2C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr26Fe59.5P14.5\\n\",\n        \"output\": \" Yes, Cr26Fe59.5P14.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb3SiMo\\n\",\n        \"output\": \" Yes, Nb3SiMo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y(MgNi)2\\n\",\n        \"output\": \" No, Y(MgNi)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.85Ti0.15Ni33\\n\",\n        \"output\": \" Yes, Zr66.85Ti0.15Ni33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti7Al2Cu\\n\",\n        \"output\": \" No, Ti7Al2Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe55Cu32Ag13\\n\",\n        \"output\": \" No, Fe55Cu32Ag13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10Fe89.964Ge0.036\\n\",\n        \"output\": \" Yes, Zr10Fe89.964Ge0.036 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg39Ti41Al20\\n\",\n        \"output\": \" No, Mg39Ti41Al20 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La11Al7Ni2\\n\",\n        \"output\": \" Yes, La11Al7Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Ni77P20\\n\",\n        \"output\": \" Yes, Ti3Ni77P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Fe89.982Ge0.018\\n\",\n        \"output\": \" Yes, Zr10Fe89.982Ge0.018 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al2(Co11B5)3\\n\",\n        \"output\": \" Yes, Al2(Co11B5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrTi4Si15\\n\",\n        \"output\": \" Yes, ZrTi4Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe7CoB2\\n\",\n        \"output\": \" Yes, Fe7CoB2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co7(Ni25P6)3\\n\",\n        \"output\": \" Yes, Co7(Ni25P6)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al3Cu\\n\",\n        \"output\": \" No, Al3Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti12FeCu7\\n\",\n        \"output\": \" Yes, Ti12FeCu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn12Co7B6\\n\",\n        \"output\": \" Yes, Mn12Co7B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Mg13Ni5\\n\",\n        \"output\": \" Yes, Nd2Mg13Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al2Ni35B13\\n\",\n        \"output\": \" Yes, Al2Ni35B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe54.5Ni18.5B27\\n\",\n        \"output\": \" Yes, Fe54.5Ni18.5B27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si2BMo17\\n\",\n        \"output\": \" No, Si2BMo17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe31Ni10B9\\n\",\n        \"output\": \" Yes, Fe31Ni10B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al57Cr23Si20\\n\",\n        \"output\": \" No, Al57Cr23Si20 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg7(Ti12Al19)3\\n\",\n        \"output\": \" Yes, Mg7(Ti12Al19)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti8AlCu11\\n\",\n        \"output\": \" Yes, Ti8AlCu11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr66.9Fe33Ni0.1\\n\",\n        \"output\": \" Yes, Zr66.9Fe33Ni0.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La(AlCu2)3\\n\",\n        \"output\": \" No, La(AlCu2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y7(Al26Ni5)3\\n\",\n        \"output\": \" Yes, Y7(Al26Ni5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Al7Cu41\\n\",\n        \"output\": \" No, Nd2Al7Cu41 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb8.9Fe79.6B11.5\\n\",\n        \"output\": \" Yes, Nb8.9Fe79.6B11.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co89B11\\n\",\n        \"output\": \" Yes, Co89B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd6MgNi3\\n\",\n        \"output\": \" Yes, Nd6MgNi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce17Al71Fe12\\n\",\n        \"output\": \" No, Ce17Al71Fe12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15Ti4Si\\n\",\n        \"output\": \" Yes, Zr15Ti4Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si22.5Ni65C12.5\\n\",\n        \"output\": \" Yes, Si22.5Ni65C12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe17Cu8\\n\",\n        \"output\": \" No, Fe17Cu8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr25Fe57.5P17.5\\n\",\n        \"output\": \" Yes, Cr25Fe57.5P17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co14Mo7C4\\n\",\n        \"output\": \" Yes, Co14Mo7C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al43Fe5Ni2\\n\",\n        \"output\": \" No, Al43Fe5Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La14Al5Ni\\n\",\n        \"output\": \" Yes, La14Al5Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr3NiP\\n\",\n        \"output\": \" Yes, Cr3NiP has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al63Cr19Si18\\n\",\n        \"output\": \" No, Al63Cr19Si18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti15(Nb4Si)7\\n\",\n        \"output\": \" Yes, Ti15(Nb4Si)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Mg11Ni6\\n\",\n        \"output\": \" Yes, Nd3Mg11Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Pd83.5\\n\",\n        \"output\": \" Yes, Si16.5Pd83.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr30Ni17B3\\n\",\n        \"output\": \" Yes, Zr30Ni17B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13AlNi6\\n\",\n        \"output\": \" Yes, Zr13AlNi6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu12.5Si17Pd70.5\\n\",\n        \"output\": \" Yes, Cu12.5Si17Pd70.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y5Al41Ni4\\n\",\n        \"output\": \" Yes, Y5Al41Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al42FeCo7\\n\",\n        \"output\": \" No, Al42FeCo7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ni4.2Pd79.3\\n\",\n        \"output\": \" Yes, Si16.5Ni4.2Pd79.3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La8(Al9Ni5)3\\n\",\n        \"output\": \" Yes, La8(Al9Ni5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Al3Cu44\\n\",\n        \"output\": \" No, Nd3Al3Cu44 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co80W7.5C12.5\\n\",\n        \"output\": \" No, Co80W7.5C12.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce4Al3Cu43\\n\",\n        \"output\": \" No, Ce4Al3Cu43 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" VFe17B2\\n\",\n        \"output\": \" No, VFe17B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" system\\n\",\n        \"output\": \" system is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr2Fe18B5\\n\",\n        \"output\": \" Yes, Cr2Fe18B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe43Ni40B17\\n\",\n        \"output\": \" Yes, Fe43Ni40B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn16.8Co67.2B16\\n\",\n        \"output\": \" Yes, Mn16.8Co67.2B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr8.5La63.5Cu28\\n\",\n        \"output\": \" Yes, Sr8.5La63.5Cu28 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr8Ni17\\n\",\n        \"output\": \" Yes, Zr8Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg15Cu2\\n\",\n        \"output\": \" Yes, Nd3Mg15Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" brazil\\n\",\n        \"output\": \" brazil is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe18.5Ni54.5B27\\n\",\n        \"output\": \" Yes, Fe18.5Ni54.5B27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe80.5P13C6.5\\n\",\n        \"output\": \" Yes, Fe80.5P13C6.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd19.4Co72.8Mo7.8\\n\",\n        \"output\": \" Yes, Gd19.4Co72.8Mo7.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe70Si12.5C17.5\\n\",\n        \"output\": \" Yes, Fe70Si12.5C17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SmAl9\\n\",\n        \"output\": \" Yes, SmAl9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrFe4Co5\\n\",\n        \"output\": \" Yes, ZrFe4Co5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnFe83B16\\n\",\n        \"output\": \" Yes, MnFe83B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10(Fe9Co)9\\n\",\n        \"output\": \" Yes, Zr10(Fe9Co)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta40Ni59Ir\\n\",\n        \"output\": \" Yes, Ta40Ni59Ir has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl18Cu\\n\",\n        \"output\": \" No, CeAl18Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La13Al5Ni2\\n\",\n        \"output\": \" Yes, La13Al5Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni21B23C6\\n\",\n        \"output\": \" Yes, Ni21B23C6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2Al20Ni3\\n\",\n        \"output\": \" Yes, Nd2Al20Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al15V2Cu3\\n\",\n        \"output\": \" Yes, Al15V2Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg7Cu2\\n\",\n        \"output\": \" Yes, CeMg7Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg13Ni4\\n\",\n        \"output\": \" Yes, Nd3Mg13Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al10V3Ge7\\n\",\n        \"output\": \" No, Al10V3Ge7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr15Si302\\n\",\n        \"output\": \" Yes, Zr15Si302 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Cu87Ag10\\n\",\n        \"output\": \" No, Ce3Cu87Ag10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al52Fe23Ge25\\n\",\n        \"output\": \" Yes, Al52Fe23Ge25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Mg17\\n\",\n        \"output\": \" No, Nd3Mg17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79Ni5B16\\n\",\n        \"output\": \" Yes, Fe79Ni5B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3AlNi6\\n\",\n        \"output\": \" Yes, La3AlNi6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Al3Ni4\\n\",\n        \"output\": \" Yes, Zr3Al3Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe22BMo2\\n\",\n        \"output\": \" No, Fe22BMo2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe15SiB4\\n\",\n        \"output\": \" Yes, Fe15SiB4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15Cr2Si3\\n\",\n        \"output\": \" Yes, Zr15Cr2Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe19Ni21B10\\n\",\n        \"output\": \" Yes, Fe19Ni21B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf43(Nb14Si5)3\\n\",\n        \"output\": \" Yes, Hf43(Nb14Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co77.5Si12.5B10\\n\",\n        \"output\": \" Yes, Co77.5Si12.5B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al15VCu4\\n\",\n        \"output\": \" Yes, Al15VCu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg15Ti32Al53\\n\",\n        \"output\": \" Yes, Mg15Ti32Al53 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" crocodile\\n\",\n        \"output\": \" crocodile is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al44Fe5Si\\n\",\n        \"output\": \" No, Al44Fe5Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe31Cu10B9\\n\",\n        \"output\": \" No, Fe31Cu10B9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni23B27\\n\",\n        \"output\": \" No, Ni23B27 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La13Al85Ni2\\n\",\n        \"output\": \" Yes, La13Al85Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe13Ni2B5\\n\",\n        \"output\": \" Yes, Fe13Ni2B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti8(Nb3Si)3\\n\",\n        \"output\": \" Yes, Ti8(Nb3Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaAl9\\n\",\n        \"output\": \" Yes, LaAl9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5Al44Ni\\n\",\n        \"output\": \" Yes, Nd5Al44Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe22B3\\n\",\n        \"output\": \" Yes, Fe22B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnSi5Pd19\\n\",\n        \"output\": \" Yes, MnSi5Pd19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti4(SiNi)3\\n\",\n        \"output\": \" No, Ti4(SiNi)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Sm4Al15Ni\\n\",\n        \"output\": \" No, Sm4Al15Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni18P5Pd2\\n\",\n        \"output\": \" Yes, Ni18P5Pd2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni31Mo10C9\\n\",\n        \"output\": \" No, Ni31Mo10C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti5Nb3Si2\\n\",\n        \"output\": \" No, Ti5Nb3Si2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al89Co2Ni9\\n\",\n        \"output\": \" No, Al89Co2Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co20.9Si16.5Pd62.6\\n\",\n        \"output\": \" No, Co20.9Si16.5Pd62.6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb20Si3C2\\n\",\n        \"output\": \" Yes, Nb20Si3C2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf(Cu2Ni)3\\n\",\n        \"output\": \" No, Hf(Cu2Ni)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg11Al4Ag5\\n\",\n        \"output\": \" Yes, Mg11Al4Ag5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Al18Ni23\\n\",\n        \"output\": \" Yes, La9Al18Ni23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2Mg17Ni\\n\",\n        \"output\": \" Yes, Y2Mg17Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Fe87B10\\n\",\n        \"output\": \" Yes, Zr3Fe87B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Fe20B3\\n\",\n        \"output\": \" Yes, Zr2Fe20B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd9.2Fe74.8B16\\n\",\n        \"output\": \" Yes, Nd9.2Fe74.8B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr17.5Cr10Co72.5\\n\",\n        \"output\": \" Yes, Zr17.5Cr10Co72.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeCu12Ag7\\n\",\n        \"output\": \" Yes, CeCu12Ag7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43FeNi6\\n\",\n        \"output\": \" Yes, Al43FeNi6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" antarctica\\n\",\n        \"output\": \" antarctica is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb9.6Fe77B13.4\\n\",\n        \"output\": \" Yes, Nb9.6Fe77B13.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al45Fe2Ni3\\n\",\n        \"output\": \" No, Al45Fe2Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg15Cu2\\n\",\n        \"output\": \" Yes, Y3Mg15Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr57.5Cu35B7.5\\n\",\n        \"output\": \" Yes, Zr57.5Cu35B7.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg33Al67\\n\",\n        \"output\": \" No, Mg33Al67 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CuNi41P8\\n\",\n        \"output\": \" No, CuNi41P8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe75Si7.5B17.5\\n\",\n        \"output\": \" Yes, Fe75Si7.5B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu6(SiPd3)11\\n\",\n        \"output\": \" Yes, Cu6(SiPd3)11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CrNi3B\\n\",\n        \"output\": \" Yes, CrNi3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu2Si17.25Pd80.75\\n\",\n        \"output\": \" Yes, Cu2Si17.25Pd80.75 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf53Nb32Si15\\n\",\n        \"output\": \" Yes, Hf53Nb32Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeNbAl8\\n\",\n        \"output\": \" Yes, CeNbAl8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Ni40Pd43.5\\n\",\n        \"output\": \" Yes, Si16.5Ni40Pd43.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15Si3Ru2\\n\",\n        \"output\": \" Yes, Zr15Si3Ru2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al71Fe15Cu14\\n\",\n        \"output\": \" Yes, Al71Fe15Cu14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti28Nb15Si7\\n\",\n        \"output\": \" Yes, Ti28Nb15Si7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87Co2Ni11\\n\",\n        \"output\": \" Yes, Al87Co2Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al7Cr2Si\\n\",\n        \"output\": \" No, Al7Cr2Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca7.5Al87.5Fe5\\n\",\n        \"output\": \" Yes, Ca7.5Al87.5Fe5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd(Mg2Ni)3\\n\",\n        \"output\": \" Yes, Nd(Mg2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3AlNi6\\n\",\n        \"output\": \" Yes, Zr3AlNi6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr67Fe16.5Ni16.5\\n\",\n        \"output\": \" Yes, Zr67Fe16.5Ni16.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg13Ti19Al68\\n\",\n        \"output\": \" No, Mg13Ti19Al68 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf13Cu4Ni3\\n\",\n        \"output\": \" Yes, Hf13Cu4Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti7Al13\\n\",\n        \"output\": \" No, Ti7Al13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2AlCu22\\n\",\n        \"output\": \" No, Nd2AlCu22 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd7Al85Ni8\\n\",\n        \"output\": \" Yes, Nd7Al85Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe89CuB10\\n\",\n        \"output\": \" No, Fe89CuB10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co5Ni75.5P19.5\\n\",\n        \"output\": \" Yes, Co5Ni75.5P19.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Ni3\\n\",\n        \"output\": \" Yes, Zr2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca3MgGa\\n\",\n        \"output\": \" Yes, Ca3MgGa has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y3Al13Ni4\\n\",\n        \"output\": \" Yes, Y3Al13Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe82CoB17\\n\",\n        \"output\": \" Yes, Fe82CoB17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr66.95Ti0.05Ni33\\n\",\n        \"output\": \" Yes, Zr66.95Ti0.05Ni33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti15SiNi4\\n\",\n        \"output\": \" Yes, Ti15SiNi4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr4Fe13B3\\n\",\n        \"output\": \" Yes, Cr4Fe13B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Fe77B19\\n\",\n        \"output\": \" Yes, Nd4Fe77B19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf11Cu4Ni5\\n\",\n        \"output\": \" Yes, Hf11Cu4Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe33.5Ni50.5B16\\n\",\n        \"output\": \" Yes, Fe33.5Ni50.5B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf7Cu2Ni\\n\",\n        \"output\": \" Yes, Hf7Cu2Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al62Fe17Cu21\\n\",\n        \"output\": \" No, Al62Fe17Cu21 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf82(NbSi5)3\\n\",\n        \"output\": \" Yes, Hf82(NbSi5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ag4.2Pd79.3\\n\",\n        \"output\": \" Yes, Si16.5Ag4.2Pd79.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr40.9Nb5Cu54.1\\n\",\n        \"output\": \" Yes, Zr40.9Nb5Cu54.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La4Al45Ni\\n\",\n        \"output\": \" Yes, La4Al45Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl18Fe\\n\",\n        \"output\": \" Yes, CeAl18Fe has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y2(Mg5Cu)3\\n\",\n        \"output\": \" Yes, Y2(Mg5Cu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" caution\\n\",\n        \"output\": \" caution is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr8.3Cr2Co89.7\\n\",\n        \"output\": \" Yes, Zr8.3Cr2Co89.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni9C\\n\",\n        \"output\": \" No, Ni9C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce4Al13Fe3\\n\",\n        \"output\": \" No, Ce4Al13Fe3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr66.95Co33Ni0.05\\n\",\n        \"output\": \" Yes, Zr66.95Co33Ni0.05 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce23Al60Fe17\\n\",\n        \"output\": \" No, Ce23Al60Fe17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAl15Ni4\\n\",\n        \"output\": \" Yes, CeAl15Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" hole\\n\",\n        \"output\": \" hole is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co7WC2\\n\",\n        \"output\": \" No, Co7WC2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr21AlNi3\\n\",\n        \"output\": \" Yes, Zr21AlNi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2Fe7B\\n\",\n        \"output\": \" Yes, Nd2Fe7B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe34W5C11\\n\",\n        \"output\": \" Yes, Fe34W5C11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2Al41Ni7\\n\",\n        \"output\": \" Yes, Nd2Al41Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti17Cu33\\n\",\n        \"output\": \" No, Ti17Cu33 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaMg5Ni4\\n\",\n        \"output\": \" Yes, LaMg5Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" drink\\n\",\n        \"output\": \" drink is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CeCu18Ag\\n\",\n        \"output\": \" No, CeCu18Ag does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe87B8Mo5\\n\",\n        \"output\": \" No, Fe87B8Mo5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La7Al29Ni14\\n\",\n        \"output\": \" Yes, La7Al29Ni14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4FeCu5\\n\",\n        \"output\": \" Yes, Zr4FeCu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaMg2Cu\\n\",\n        \"output\": \" No, LaMg2Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd11Al9\\n\",\n        \"output\": \" Yes, Gd11Al9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Fe77B16\\n\",\n        \"output\": \" Yes, Zr7Fe77B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe20Si2B3\\n\",\n        \"output\": \" Yes, Fe20Si2B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co3.5Ni74.5P22\\n\",\n        \"output\": \" No, Co3.5Ni74.5P22 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CuNi83P16\\n\",\n        \"output\": \" No, CuNi83P16 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co15B9C\\n\",\n        \"output\": \" Yes, Co15B9C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe75B21P4\\n\",\n        \"output\": \" Yes, Fe75B21P4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaMg13Cu6\\n\",\n        \"output\": \" Yes, LaMg13Cu6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdAlCu23\\n\",\n        \"output\": \" No, NdAlCu23 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe19B5W\\n\",\n        \"output\": \" Yes, Fe19B5W has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Cu6Ni\\n\",\n        \"output\": \" Yes, Ti3Cu6Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni7B3\\n\",\n        \"output\": \" Yes, Ni7B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnFe95B4\\n\",\n        \"output\": \" No, MnFe95B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr17Ti3\\n\",\n        \"output\": \" Yes, Zr17Ti3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti5Al54Ni41\\n\",\n        \"output\": \" No, Ti5Al54Ni41 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" V15Fe71B14\\n\",\n        \"output\": \" Yes, V15Fe71B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti5CuNi4\\n\",\n        \"output\": \" No, Ti5CuNi4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti13Al7\\n\",\n        \"output\": \" No, Ti13Al7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaNi\\n\",\n        \"output\": \" No, LaNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La11Cu44.5Au44.5\\n\",\n        \"output\": \" Yes, La11Cu44.5Au44.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si9Pd41\\n\",\n        \"output\": \" Yes, Si9Pd41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaAl8Ni\\n\",\n        \"output\": \" Yes, LaAl8Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe16.5Co66.5B17\\n\",\n        \"output\": \" Yes, Fe16.5Co66.5B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CaAl17Ni2\\n\",\n        \"output\": \" No, CaAl17Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr(CrCo2)3\\n\",\n        \"output\": \" Yes, Zr(CrCo2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg18Ni\\n\",\n        \"output\": \" No, CeMg18Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb4Si\\n\",\n        \"output\": \" Yes, Nb4Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg7Ni3\\n\",\n        \"output\": \" No, Mg7Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" yacht\\n\",\n        \"output\": \" yacht is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" mark\\n\",\n        \"output\": \" mark is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr69.6Ni16.2P14.2\\n\",\n        \"output\": \" No, Cr69.6Ni16.2P14.2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe61Ni25B14\\n\",\n        \"output\": \" Yes, Fe61Ni25B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg15Cu4\\n\",\n        \"output\": \" Yes, CeMg15Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La13(Al27Ni2)3\\n\",\n        \"output\": \" Yes, La13(Al27Ni2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca6MgGa3\\n\",\n        \"output\": \" Yes, Ca6MgGa3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca3La59.5Cu37.5\\n\",\n        \"output\": \" Yes, Ca3La59.5Cu37.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn13Co31B6\\n\",\n        \"output\": \" Yes, Mn13Co31B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co19(B2C)2\\n\",\n        \"output\": \" Yes, Co19(B2C)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al3Fe80P17\\n\",\n        \"output\": \" Yes, Al3Fe80P17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg5Cu2\\n\",\n        \"output\": \" Yes, Y3Mg5Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6(Fe3B)11\\n\",\n        \"output\": \" Yes, Al6(Fe3B)11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CrFe18C\\n\",\n        \"output\": \" No, CrFe18C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaAl5Cu4\\n\",\n        \"output\": \" No, LaAl5Cu4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe83SiB16\\n\",\n        \"output\": \" Yes, Fe83SiB16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti10Al3Cu7\\n\",\n        \"output\": \" Yes, Ti10Al3Cu7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" FeNi3B\\n\",\n        \"output\": \" Yes, FeNi3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Al3Cu44\\n\",\n        \"output\": \" No, Ce3Al3Cu44 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr83Ti12Si5\\n\",\n        \"output\": \" Yes, Zr83Ti12Si5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti21Nb22Cu57\\n\",\n        \"output\": \" Yes, Ti21Nb22Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg14Cu3\\n\",\n        \"output\": \" Yes, Y3Mg14Cu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn7Co27B16\\n\",\n        \"output\": \" Yes, Mn7Co27B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr87P13\\n\",\n        \"output\": \" No, Cr87P13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3Ni\\n\",\n        \"output\": \" No, Ti3Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu83.5Ag8.9P7.6\\n\",\n        \"output\": \" Yes, Cu83.5Ag8.9P7.6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si2Ni20B3\\n\",\n        \"output\": \" No, Si2Ni20B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10Cu9B\\n\",\n        \"output\": \" Yes, Zr10Cu9B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La8(Mg3Cu)3\\n\",\n        \"output\": \" Yes, La8(Mg3Cu)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" sister-in-law\\n\",\n        \"output\": \" sister-in-law is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co41B9\\n\",\n        \"output\": \" Yes, Co41B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd9Al83Ni8\\n\",\n        \"output\": \" Yes, Nd9Al83Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd5AlCu44\\n\",\n        \"output\": \" No, Nd5AlCu44 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Al5Cu2\\n\",\n        \"output\": \" No, Ti3Al5Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Fe67.5Co22.5\\n\",\n        \"output\": \" Yes, Zr10Fe67.5Co22.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co15W3C2\\n\",\n        \"output\": \" No, Co15W3C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co82.5W7.5C10\\n\",\n        \"output\": \" No, Co82.5W7.5C10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe70Si17.5B12.5\\n\",\n        \"output\": \" Yes, Fe70Si17.5B12.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg17Al2Zn\\n\",\n        \"output\": \" No, Mg17Al2Zn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe75Si3B22\\n\",\n        \"output\": \" Yes, Fe75Si3B22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg5Ni2\\n\",\n        \"output\": \" Yes, Nd3Mg5Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SiB4Mo15\\n\",\n        \"output\": \" Yes, SiB4Mo15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnAl47Co2\\n\",\n        \"output\": \" No, MnAl47Co2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg7Ti49Al44\\n\",\n        \"output\": \" Yes, Mg7Ti49Al44 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe83B5P12\\n\",\n        \"output\": \" Yes, Fe83B5P12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf54V31Si15\\n\",\n        \"output\": \" Yes, Hf54V31Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti31Be19\\n\",\n        \"output\": \" Yes, Ti31Be19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Al12Ni29\\n\",\n        \"output\": \" Yes, La9Al12Ni29 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co17C3\\n\",\n        \"output\": \" No, Co17C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMg2Cu\\n\",\n        \"output\": \" No, CeMg2Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si20Ag4.5Pd75.5\\n\",\n        \"output\": \" Yes, Si20Ag4.5Pd75.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2.5Mg95.5Mn2\\n\",\n        \"output\": \" No, Y2.5Mg95.5Mn2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg44Al43Pd13\\n\",\n        \"output\": \" No, Mg44Al43Pd13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl49\\n\",\n        \"output\": \" No, NdAl49 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr3Ni13P4\\n\",\n        \"output\": \" Yes, Cr3Ni13P4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti16CuNi3\\n\",\n        \"output\": \" No, Ti16CuNi3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe20B4C\\n\",\n        \"output\": \" Yes, Fe20B4C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co19B5C\\n\",\n        \"output\": \" Yes, Co19B5C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr14Al5Ni\\n\",\n        \"output\": \" Yes, Zr14Al5Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe4B\\n\",\n        \"output\": \" Yes, Fe4B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La24Al59Ni17\\n\",\n        \"output\": \" Yes, La24Al59Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg11Ti29Al60\\n\",\n        \"output\": \" Yes, Mg11Ti29Al60 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Ag6.7Pd76.8\\n\",\n        \"output\": \" Yes, Si16.5Ag6.7Pd76.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr7Fe76P17\\n\",\n        \"output\": \" Yes, Cr7Fe76P17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Al3Ni4\\n\",\n        \"output\": \" Yes, La3Al3Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn3Al42Ni5\\n\",\n        \"output\": \" No, Mn3Al42Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni35B14C\\n\",\n        \"output\": \" Yes, Ni35B14C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr22Co19C9\\n\",\n        \"output\": \" Yes, Cr22Co19C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al89Fe6Ni5\\n\",\n        \"output\": \" No, Al89Fe6Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al84Fe3Ni13\\n\",\n        \"output\": \" No, Al84Fe3Ni13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Ni11.7Pd71.8\\n\",\n        \"output\": \" Yes, Si16.5Ni11.7Pd71.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti15V2Si3\\n\",\n        \"output\": \" Yes, Ti15V2Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Ni50.1Pd33.4\\n\",\n        \"output\": \" Yes, Si16.5Ni50.1Pd33.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb7.3Fe79.5B13.2\\n\",\n        \"output\": \" Yes, Nb7.3Fe79.5B13.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni4B\\n\",\n        \"output\": \" No, Ni4B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al10Ni33B7\\n\",\n        \"output\": \" No, Al10Ni33B7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe87Cu5B8\\n\",\n        \"output\": \" No, Fe87Cu5B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y4Al15Ni\\n\",\n        \"output\": \" No, Y4Al15Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe69Si7B24\\n\",\n        \"output\": \" Yes, Fe69Si7B24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr13.5La56Cu30.5\\n\",\n        \"output\": \" Yes, Sr13.5La56Cu30.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al8(Ni11B3)3\\n\",\n        \"output\": \" Yes, Al8(Ni11B3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta3Ni7\\n\",\n        \"output\": \" Yes, Ta3Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7Ni18\\n\",\n        \"output\": \" No, Ti7Ni18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti8(Co11B3)3\\n\",\n        \"output\": \" Yes, Ti8(Co11B3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca8.5La56.5Cu35\\n\",\n        \"output\": \" Yes, Ca8.5La56.5Cu35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si(Ni5B)4\\n\",\n        \"output\": \" No, Si(Ni5B)4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf30.1Nb30Cu39.9\\n\",\n        \"output\": \" Yes, Hf30.1Nb30Cu39.9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb7.1Fe82.3B10.6\\n\",\n        \"output\": \" No, Nb7.1Fe82.3B10.6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce8Cu37Ag55\\n\",\n        \"output\": \" Yes, Ce8Cu37Ag55 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr33Ti12Si5\\n\",\n        \"output\": \" Yes, Zr33Ti12Si5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2(Al5Co)3\\n\",\n        \"output\": \" No, Ce2(Al5Co)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al6Co39B5\\n\",\n        \"output\": \" No, Al6Co39B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti5SiNi4\\n\",\n        \"output\": \" Yes, Ti5SiNi4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg17Cu2\\n\",\n        \"output\": \" Yes, YMg17Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr37SiNi12\\n\",\n        \"output\": \" Yes, Zr37SiNi12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" comparison\\n\",\n        \"output\": \" comparison is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6Ti5Si9\\n\",\n        \"output\": \" Yes, Zr6Ti5Si9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf5Cu3Ni2\\n\",\n        \"output\": \" Yes, Hf5Cu3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YAl44Ni5\\n\",\n        \"output\": \" Yes, YAl44Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co33Ni33B34\\n\",\n        \"output\": \" Yes, Co33Ni33B34 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7Ti4Cu9\\n\",\n        \"output\": \" Yes, Zr7Ti4Cu9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe15CuB4\\n\",\n        \"output\": \" No, Fe15CuB4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co3SiB\\n\",\n        \"output\": \" No, Co3SiB does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf33Nb10Cu57\\n\",\n        \"output\": \" Yes, Hf33Nb10Cu57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAlCu8\\n\",\n        \"output\": \" No, CeAlCu8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al43Ni7\\n\",\n        \"output\": \" No, Al43Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La7Mg71Zn22\\n\",\n        \"output\": \" Yes, La7Mg71Zn22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2(Al5Cu)3\\n\",\n        \"output\": \" Yes, Ce2(Al5Cu)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg16AlZn3\\n\",\n        \"output\": \" No, Mg16AlZn3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Mg2Ni5\\n\",\n        \"output\": \" Yes, Nd3Mg2Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrVCo8\\n\",\n        \"output\": \" Yes, ZrVCo8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd14Fe81B5\\n\",\n        \"output\": \" No, Nd14Fe81B5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2Al2Ni\\n\",\n        \"output\": \" Yes, La2Al2Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti9Al5Cu6\\n\",\n        \"output\": \" No, Ti9Al5Cu6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni8BC\\n\",\n        \"output\": \" No, Ni8BC does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe17B3\\n\",\n        \"output\": \" Yes, Fe17B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5P17.5C5\\n\",\n        \"output\": \" Yes, Fe77.5P17.5C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn38.5Co41.5B20\\n\",\n        \"output\": \" Yes, Mn38.5Co41.5B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La2Mg2Ni\\n\",\n        \"output\": \" No, La2Mg2Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn17.4Al68.6Si14\\n\",\n        \"output\": \" No, Mn17.4Al68.6Si14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn17Co25B8\\n\",\n        \"output\": \" Yes, Mn17Co25B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr4(Ti2Si5)3\\n\",\n        \"output\": \" Yes, Zr4(Ti2Si5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba4(La23Cu9)3\\n\",\n        \"output\": \" Yes, Ba4(La23Cu9)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79(B2P5)3\\n\",\n        \"output\": \" Yes, Fe79(B2P5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al13VGe6\\n\",\n        \"output\": \" No, Al13VGe6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr5Fe38B7\\n\",\n        \"output\": \" Yes, Cr5Fe38B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Ni35Pd48.5\\n\",\n        \"output\": \" Yes, Si16.5Ni35Pd48.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe6Co77B17\\n\",\n        \"output\": \" Yes, Fe6Co77B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Al10Cu\\n\",\n        \"output\": \" No, Ti9Al10Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La27Al11Ni62\\n\",\n        \"output\": \" Yes, La27Al11Ni62 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5Al2Cu43\\n\",\n        \"output\": \" No, Nd5Al2Cu43 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAl5Ge4\\n\",\n        \"output\": \" Yes, MnAl5Ge4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5(FeCo4)9\\n\",\n        \"output\": \" Yes, Zr5(FeCo4)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn33.5Co50.5B16\\n\",\n        \"output\": \" Yes, Mn33.5Co50.5B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl5Ni4\\n\",\n        \"output\": \" No, LaAl5Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg13Ti12\\n\",\n        \"output\": \" No, Mg13Ti12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YAl8Ni\\n\",\n        \"output\": \" Yes, YAl8Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr4P\\n\",\n        \"output\": \" No, Cr4P does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu37.5Ag37.5Ge25\\n\",\n        \"output\": \" Yes, Cu37.5Ag37.5Ge25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y5Mg2Ag3\\n\",\n        \"output\": \" No, Y5Mg2Ag3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co18B3C4\\n\",\n        \"output\": \" No, Co18B3C4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni14B10C\\n\",\n        \"output\": \" No, Ni14B10C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti9AlNi10\\n\",\n        \"output\": \" No, Ti9AlNi10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3Fe17\\n\",\n        \"output\": \" Yes, Nd3Fe17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" siberian\\n\",\n        \"output\": \" siberian is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni23(B7C2)3\\n\",\n        \"output\": \" Yes, Ni23(B7C2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5(Nb4Ge)3\\n\",\n        \"output\": \" Yes, Zr5(Nb4Ge)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y2.5Mg87.5Mn10\\n\",\n        \"output\": \" No, Y2.5Mg87.5Mn10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg5Ni2\\n\",\n        \"output\": \" Yes, La3Mg5Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni6P5Pt9\\n\",\n        \"output\": \" Yes, Ni6P5Pt9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mo16P5Ru4\\n\",\n        \"output\": \" Yes, Mo16P5Ru4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39B6Mo5\\n\",\n        \"output\": \" Yes, Fe39B6Mo5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co37Mo6C7\\n\",\n        \"output\": \" No, Co37Mo6C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe79(BP6)3\\n\",\n        \"output\": \" Yes, Fe79(BP6)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7Co2B\\n\",\n        \"output\": \" Yes, Ti7Co2B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5Mg2Ni3\\n\",\n        \"output\": \" Yes, Nd5Mg2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe5Ni11P4\\n\",\n        \"output\": \" Yes, Fe5Ni11P4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" writer\\n\",\n        \"output\": \" writer is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe77Co6B17\\n\",\n        \"output\": \" Yes, Fe77Co6B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg4Ni3\\n\",\n        \"output\": \" Yes, Y3Mg4Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" surprise\\n\",\n        \"output\": \" surprise is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe8SiP\\n\",\n        \"output\": \" Yes, Fe8SiP has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr7Fe39B4\\n\",\n        \"output\": \" No, Cr7Fe39B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y4Al11Ni5\\n\",\n        \"output\": \" Yes, Y4Al11Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co4.2Si16.5Pd79.3\\n\",\n        \"output\": \" Yes, Co4.2Si16.5Pd79.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si17Pd71Au12\\n\",\n        \"output\": \" Yes, Si17Pd71Au12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7VSi2\\n\",\n        \"output\": \" Yes, Nb7VSi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La11Al5Co4\\n\",\n        \"output\": \" Yes, La11Al5Co4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al17Cr2Si\\n\",\n        \"output\": \" No, Al17Cr2Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" request\\n\",\n        \"output\": \" request is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti4Be\\n\",\n        \"output\": \" No, Ti4Be does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni28B19C3\\n\",\n        \"output\": \" Yes, Ni28B19C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al2Ni5B3\\n\",\n        \"output\": \" Yes, Al2Ni5B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce(CuAg2)3\\n\",\n        \"output\": \" No, Ce(CuAg2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" furniture\\n\",\n        \"output\": \" furniture is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83B2.3P14.7\\n\",\n        \"output\": \" Yes, Fe83B2.3P14.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca6AlGa3\\n\",\n        \"output\": \" Yes, Ca6AlGa3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn6Al69Ge25\\n\",\n        \"output\": \" Yes, Mn6Al69Ge25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ash\\n\",\n        \"output\": \" ash is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti9Al5Ni6\\n\",\n        \"output\": \" Yes, Ti9Al5Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al3VGe\\n\",\n        \"output\": \" No, Al3VGe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al87Fe5Ni8\\n\",\n        \"output\": \" No, Al87Fe5Ni8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd33.6Fe50.4B16\\n\",\n        \"output\": \" Yes, Nd33.6Fe50.4B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr67Fe13.2Ni19.8\\n\",\n        \"output\": \" Yes, Zr67Fe13.2Ni19.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn15Fe71B14\\n\",\n        \"output\": \" Yes, Mn15Fe71B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti14(VSi)3\\n\",\n        \"output\": \" Yes, Ti14(VSi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe3Ni5B2\\n\",\n        \"output\": \" Yes, Fe3Ni5B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5Si10B12.5\\n\",\n        \"output\": \" Yes, Fe77.5Si10B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe38SiB11\\n\",\n        \"output\": \" No, Fe38SiB11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe81B12P7\\n\",\n        \"output\": \" Yes, Fe81B12P7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta40Ni59Ru\\n\",\n        \"output\": \" Yes, Ta40Ni59Ru has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni7BC2\\n\",\n        \"output\": \" No, Ni7BC2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Fe18B5\\n\",\n        \"output\": \" Yes, Zr2Fe18B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr14(CrNi)3\\n\",\n        \"output\": \" Yes, Zr14(CrNi)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce4(Cu17Ag15)3\\n\",\n        \"output\": \" Yes, Ce4(Cu17Ag15)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2AlNi2\\n\",\n        \"output\": \" Yes, Zr2AlNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg7Cu2\\n\",\n        \"output\": \" Yes, YMg7Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb8Fe79B13\\n\",\n        \"output\": \" Yes, Nb8Fe79B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe41SiB8\\n\",\n        \"output\": \" Yes, Fe41SiB8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf72V13Si15\\n\",\n        \"output\": \" Yes, Hf72V13Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg13Ni6\\n\",\n        \"output\": \" Yes, YMg13Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni41P9\\n\",\n        \"output\": \" Yes, Ni41P9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf11(Nb2Si)3\\n\",\n        \"output\": \" Yes, Hf11(Nb2Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al11Cr5Si4\\n\",\n        \"output\": \" No, Al11Cr5Si4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La37Al53Ni10\\n\",\n        \"output\": \" Yes, La37Al53Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMn5Al44\\n\",\n        \"output\": \" No, CeMn5Al44 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr20Fe23C7\\n\",\n        \"output\": \" No, Cr20Fe23C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni2PPd2\\n\",\n        \"output\": \" Yes, Ni2PPd2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf73(Nb4Si5)3\\n\",\n        \"output\": \" Yes, Hf73(Nb4Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe8NiB\\n\",\n        \"output\": \" Yes, Fe8NiB has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Nb14Si3\\n\",\n        \"output\": \" Yes, Zr3Nb14Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce5Al4Cu41\\n\",\n        \"output\": \" Yes, Ce5Al4Cu41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg11Ni6\\n\",\n        \"output\": \" Yes, La3Mg11Ni6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6Cu3B\\n\",\n        \"output\": \" Yes, Zr6Cu3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y3Mg15Ni2\\n\",\n        \"output\": \" Yes, Y3Mg15Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" TiCu2Ni7\\n\",\n        \"output\": \" No, TiCu2Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca10Al87.5Fe2.5\\n\",\n        \"output\": \" No, Ca10Al87.5Fe2.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Al88Ni7\\n\",\n        \"output\": \" Yes, Zr5Al88Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni31Mo69\\n\",\n        \"output\": \" Yes, Ni31Mo69 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2FeCu2\\n\",\n        \"output\": \" Yes, Zr2FeCu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Mg5Ni3\\n\",\n        \"output\": \" Yes, Nd2Mg5Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Mg14Ni3\\n\",\n        \"output\": \" Yes, Y3Mg14Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu13Ni67P20\\n\",\n        \"output\": \" No, Cu13Ni67P20 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83Si11B6\\n\",\n        \"output\": \" No, Fe83Si11B6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe37W2C11\\n\",\n        \"output\": \" No, Fe37W2C11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2Al17Ni\\n\",\n        \"output\": \" Yes, La2Al17Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al87Co3Ni10\\n\",\n        \"output\": \" No, Al87Co3Ni10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn15Fe77B8\\n\",\n        \"output\": \" No, Mn15Fe77B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Gd5Al83Ni12\\n\",\n        \"output\": \" Yes, Gd5Al83Ni12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Nb14Si3\\n\",\n        \"output\": \" Yes, Ti3Nb14Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni12P5Pt8\\n\",\n        \"output\": \" Yes, Ni12P5Pt8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si9Ni38B3\\n\",\n        \"output\": \" No, Si9Ni38B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe85Si2B13\\n\",\n        \"output\": \" No, Fe85Si2B13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti14SiNi5\\n\",\n        \"output\": \" Yes, Ti14SiNi5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co14Si5C\\n\",\n        \"output\": \" No, Co14Si5C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Al46Ni\\n\",\n        \"output\": \" No, Mn3Al46Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" SiNi8B\\n\",\n        \"output\": \" Yes, SiNi8B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn22.8Co53.2B24\\n\",\n        \"output\": \" Yes, Mn22.8Co53.2B24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4Fe35B11\\n\",\n        \"output\": \" Yes, Zr4Fe35B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al53Si16Mo31\\n\",\n        \"output\": \" Yes, Al53Si16Mo31 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu7Si16.5Pd76.5\\n\",\n        \"output\": \" Yes, Cu7Si16.5Pd76.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" GdAl16Ni3\\n\",\n        \"output\": \" Yes, GdAl16Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CaMg18Zn\\n\",\n        \"output\": \" No, CaMg18Zn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Al7Fe\\n\",\n        \"output\": \" No, Ce2Al7Fe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti10SiNi9\\n\",\n        \"output\": \" No, Ti10SiNi9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La2Mg5Ni3\\n\",\n        \"output\": \" Yes, La2Mg5Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9Nb8Ge3\\n\",\n        \"output\": \" Yes, Zr9Nb8Ge3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al88Co5Ni7\\n\",\n        \"output\": \" Yes, Al88Co5Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Ti23Si65\\n\",\n        \"output\": \" Yes, Zr12Ti23Si65 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81Cu3B16\\n\",\n        \"output\": \" No, Fe81Cu3B16 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe71Mo17C12\\n\",\n        \"output\": \" Yes, Fe71Mo17C12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti87Si13\\n\",\n        \"output\": \" Yes, Ti87Si13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba3La57Cu40\\n\",\n        \"output\": \" Yes, Ba3La57Cu40 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca2Al17Ni\\n\",\n        \"output\": \" Yes, Ca2Al17Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr4Al5Ni\\n\",\n        \"output\": \" No, Zr4Al5Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnFe7B2\\n\",\n        \"output\": \" Yes, MnFe7B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdFe3\\n\",\n        \"output\": \" Yes, NdFe3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al35Fe7Ni8\\n\",\n        \"output\": \" Yes, Al35Fe7Ni8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe86.5Cu0.5B13\\n\",\n        \"output\": \" Yes, Fe86.5Cu0.5B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co15Si16.5Pd68.5\\n\",\n        \"output\": \" Yes, Co15Si16.5Pd68.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La6Mg9Ni5\\n\",\n        \"output\": \" Yes, La6Mg9Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Al9Ni7\\n\",\n        \"output\": \" Yes, Ti9Al9Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe63B37\\n\",\n        \"output\": \" Yes, Fe63B37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co7Si2B\\n\",\n        \"output\": \" No, Co7Si2B does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn35(Co3B2)3\\n\",\n        \"output\": \" Yes, Mn35(Co3B2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti12SiNi7\\n\",\n        \"output\": \" Yes, Ti12SiNi7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba67La28Cu5\\n\",\n        \"output\": \" Yes, Ba67La28Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y3Mg11Ag6\\n\",\n        \"output\": \" Yes, Y3Mg11Ag6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti7Be2Si\\n\",\n        \"output\": \" Yes, Ti7Be2Si has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al91Fe2Ni7\\n\",\n        \"output\": \" No, Al91Fe2Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5(Fe2Co3)9\\n\",\n        \"output\": \" Yes, Zr5(Fe2Co3)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe15B4Mo\\n\",\n        \"output\": \" Yes, Fe15B4Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe39Si4B7\\n\",\n        \"output\": \" Yes, Fe39Si4B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5(FeNi4)9\\n\",\n        \"output\": \" Yes, Zr5(FeNi4)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al11Si7\\n\",\n        \"output\": \" Yes, Mn2Al11Si7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe37(Cu2Ag)21\\n\",\n        \"output\": \" No, Fe37(Cu2Ag)21 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co12Mo9C4\\n\",\n        \"output\": \" Yes, Co12Mo9C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni17B2C\\n\",\n        \"output\": \" No, Ni17B2C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg9Zn\\n\",\n        \"output\": \" No, Mg9Zn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti13Al2Ni5\\n\",\n        \"output\": \" Yes, Ti13Al2Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6Ti11Si3\\n\",\n        \"output\": \" Yes, Zr6Ti11Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr9Fe38B3\\n\",\n        \"output\": \" No, Cr9Fe38B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr15La52.5Cu32.5\\n\",\n        \"output\": \" Yes, Sr15La52.5Cu32.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Pd78.5Au5\\n\",\n        \"output\": \" Yes, Si16.5Pd78.5Au5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al17Ni\\n\",\n        \"output\": \" Yes, Ce2Al17Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2Mg13Cu5\\n\",\n        \"output\": \" Yes, Ce2Mg13Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe89Ni3B8\\n\",\n        \"output\": \" No, Fe89Ni3B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15(Ni4B)2\\n\",\n        \"output\": \" Yes, Zr15(Ni4B)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Al23\\n\",\n        \"output\": \" No, Ti2Al23 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Sm4Al21\\n\",\n        \"output\": \" Yes, Sm4Al21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu80.8Ag12.2P7\\n\",\n        \"output\": \" Yes, Cu80.8Ag12.2P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5Al41Ni4\\n\",\n        \"output\": \" Yes, Nd5Al41Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr7Fe36B7\\n\",\n        \"output\": \" Yes, Cr7Fe36B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn33Fe10B7\\n\",\n        \"output\": \" Yes, Mn33Fe10B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al49Co\\n\",\n        \"output\": \" No, Al49Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" uzbekistan\\n\",\n        \"output\": \" uzbekistan is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti57Al5Cu38\\n\",\n        \"output\": \" Yes, Ti57Al5Cu38 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe72.5P12.5C15\\n\",\n        \"output\": \" Yes, Fe72.5P12.5C15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co67.5Si7.5B25\\n\",\n        \"output\": \" Yes, Co67.5Si7.5B25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn25Co59B16\\n\",\n        \"output\": \" Yes, Mn25Co59B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr3Ni5B2\\n\",\n        \"output\": \" Yes, Cr3Ni5B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr13Fe30B7\\n\",\n        \"output\": \" Yes, Cr13Fe30B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9Al5Ni6\\n\",\n        \"output\": \" Yes, Zr9Al5Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Mg13Ni3\\n\",\n        \"output\": \" Yes, Nd4Mg13Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti9Be\\n\",\n        \"output\": \" No, Ti9Be does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca6La63Cu31\\n\",\n        \"output\": \" Yes, Ca6La63Cu31 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr5Fe81B14\\n\",\n        \"output\": \" Yes, Cr5Fe81B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Al3Cu4\\n\",\n        \"output\": \" No, Ti3Al3Cu4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" FeNi79P20\\n\",\n        \"output\": \" Yes, FeNi79P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni29B21\\n\",\n        \"output\": \" Yes, Ni29B21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7Co40B3\\n\",\n        \"output\": \" Yes, Nb7Co40B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2Mg13Ag5\\n\",\n        \"output\": \" Yes, Y2Mg13Ag5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si11Ni78B11\\n\",\n        \"output\": \" Yes, Si11Ni78B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al16CrSi3\\n\",\n        \"output\": \" No, Al16CrSi3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni15(Mo3C2)2\\n\",\n        \"output\": \" Yes, Ni15(Mo3C2)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca2La60.5Cu37.5\\n\",\n        \"output\": \" Yes, Ca2La60.5Cu37.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti37Nb50Si13\\n\",\n        \"output\": \" No, Ti37Nb50Si13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si3Pd17\\n\",\n        \"output\": \" Yes, Si3Pd17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnSi4Pd15\\n\",\n        \"output\": \" Yes, MnSi4Pd15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr39Al10Ni\\n\",\n        \"output\": \" Yes, Zr39Al10Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al22Ni\\n\",\n        \"output\": \" No, Mn2Al22Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu86Ag7.5P6.5\\n\",\n        \"output\": \" No, Cu86Ag7.5P6.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu19Si16.5Pd64.5\\n\",\n        \"output\": \" Yes, Cu19Si16.5Pd64.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti4Al10Ni11\\n\",\n        \"output\": \" Yes, Ti4Al10Ni11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YMg14Ag5\\n\",\n        \"output\": \" Yes, YMg14Ag5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni18BC\\n\",\n        \"output\": \" No, Ni18BC does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAl18Cu\\n\",\n        \"output\": \" Yes, LaAl18Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti21Al22Ni7\\n\",\n        \"output\": \" Yes, Ti21Al22Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8Co37Mo5\\n\",\n        \"output\": \" Yes, Zr8Co37Mo5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr6VNi3\\n\",\n        \"output\": \" Yes, Zr6VNi3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al66.5Si18.5Ni15\\n\",\n        \"output\": \" Yes, Al66.5Si18.5Ni15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg4Al5Zn\\n\",\n        \"output\": \" No, Mg4Al5Zn does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2(TiSi5)3\\n\",\n        \"output\": \" Yes, Zr2(TiSi5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg3Cu4\\n\",\n        \"output\": \" Yes, La3Mg3Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiCu4\\n\",\n        \"output\": \" No, TiCu4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe80B17C3\\n\",\n        \"output\": \" Yes, Fe80B17C3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Mg15Cu2\\n\",\n        \"output\": \" No, Ce3Mg15Cu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13Al2Cu5\\n\",\n        \"output\": \" Yes, Zr13Al2Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" V5Fe81B14\\n\",\n        \"output\": \" Yes, V5Fe81B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeMn2Al17\\n\",\n        \"output\": \" No, CeMn2Al17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb5Fe87B8\\n\",\n        \"output\": \" No, Nb5Fe87B8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Al15Ni2\\n\",\n        \"output\": \" Yes, Nd3Al15Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn26.5Co45.5B28\\n\",\n        \"output\": \" Yes, Mn26.5Co45.5B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al23Cr2\\n\",\n        \"output\": \" No, Al23Cr2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co31Mo12C7\\n\",\n        \"output\": \" No, Co31Mo12C7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Fe15B2\\n\",\n        \"output\": \" Yes, Zr3Fe15B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Yb18Cu7\\n\",\n        \"output\": \" Yes, Yb18Cu7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Al2\\n\",\n        \"output\": \" No, Ti3Al2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe91B9\\n\",\n        \"output\": \" Yes, Fe91B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca3Mg2\\n\",\n        \"output\": \" Yes, Ca3Mg2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf77Nb8Si15\\n\",\n        \"output\": \" Yes, Hf77Nb8Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr12.5La57.5Cu30\\n\",\n        \"output\": \" Yes, Sr12.5La57.5Cu30 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg17Ni2\\n\",\n        \"output\": \" Yes, YMg17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni3P5Pt12\\n\",\n        \"output\": \" Yes, Ni3P5Pt12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CrCo3B\\n\",\n        \"output\": \" Yes, CrCo3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn13.4Co53.6B33\\n\",\n        \"output\": \" Yes, Mn13.4Co53.6B33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd2Mg17Ni\\n\",\n        \"output\": \" Yes, Nd2Mg17Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y(MgAg)2\\n\",\n        \"output\": \" Yes, Y(MgAg)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" withdrawal\\n\",\n        \"output\": \" withdrawal is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2Al7Ni\\n\",\n        \"output\": \" No, La2Al7Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co31B18C\\n\",\n        \"output\": \" Yes, Co31B18C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg5Cu2\\n\",\n        \"output\": \" Yes, La3Mg5Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3Ni17\\n\",\n        \"output\": \" No, Si3Ni17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe75Si17.5B7.5\\n\",\n        \"output\": \" Yes, Fe75Si17.5B7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La6Mg15Ni4\\n\",\n        \"output\": \" Yes, La6Mg15Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce5Al44Fe\\n\",\n        \"output\": \" Yes, Ce5Al44Fe has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al16Ni3Mo\\n\",\n        \"output\": \" Yes, Al16Ni3Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SmAl17Ni2\\n\",\n        \"output\": \" Yes, SmAl17Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg23Ti61Al16\\n\",\n        \"output\": \" No, Mg23Ti61Al16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl18Ni\\n\",\n        \"output\": \" Yes, NdAl18Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb13Si4W3\\n\",\n        \"output\": \" No, Nb13Si4W3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf18.2Fe46.2O35.6\\n\",\n        \"output\": \" Yes, Hf18.2Fe46.2O35.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5Si7.5B15\\n\",\n        \"output\": \" Yes, Fe77.5Si7.5B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co22B3\\n\",\n        \"output\": \" Yes, Co22B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co10Ni71P19\\n\",\n        \"output\": \" No, Co10Ni71P19 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf61(Nb8Si5)3\\n\",\n        \"output\": \" Yes, Hf61(Nb8Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9Al4Ni7\\n\",\n        \"output\": \" Yes, Zr9Al4Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y3Al16Ni\\n\",\n        \"output\": \" No, Y3Al16Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrAl4Ni5\\n\",\n        \"output\": \" No, ZrAl4Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Si2Ni5\\n\",\n        \"output\": \" No, Ti3Si2Ni5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni68.5B17W14.5\\n\",\n        \"output\": \" Yes, Ni68.5B17W14.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" blanket\\n\",\n        \"output\": \" blanket is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti17Ni3\\n\",\n        \"output\": \" No, Ti17Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd2Al7Ni\\n\",\n        \"output\": \" No, Gd2Al7Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn(Al8Ni)11\\n\",\n        \"output\": \" Yes, Mn(Al8Ni)11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83Ni15B2\\n\",\n        \"output\": \" No, Fe83Ni15B2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6AlNi13\\n\",\n        \"output\": \" Yes, Zr6AlNi13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" plantation\\n\",\n        \"output\": \" plantation is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti2(Nb5Si)3\\n\",\n        \"output\": \" Yes, Ti2(Nb5Si)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2Ni3\\n\",\n        \"output\": \" Yes, Ti2Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe76Ni5B19\\n\",\n        \"output\": \" Yes, Fe76Ni5B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co35W7C8\\n\",\n        \"output\": \" Yes, Co35W7C8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg15Al2Ag3\\n\",\n        \"output\": \" Yes, Mg15Al2Ag3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr7Si20Pd73\\n\",\n        \"output\": \" Yes, Cr7Si20Pd73 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni53.5B44C2.5\\n\",\n        \"output\": \" No, Ni53.5B44C2.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co17B8\\n\",\n        \"output\": \" Yes, Co17B8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al30Cr9Si11\\n\",\n        \"output\": \" No, Al30Cr9Si11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti12Nb5Si3\\n\",\n        \"output\": \" Yes, Ti12Nb5Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" skate\\n\",\n        \"output\": \" skate is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe3Ni77P20\\n\",\n        \"output\": \" Yes, Fe3Ni77P20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn32.5Co47.5B20\\n\",\n        \"output\": \" Yes, Mn32.5Co47.5B20 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl16Cu3\\n\",\n        \"output\": \" Yes, CeAl16Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe72.5P10C17.5\\n\",\n        \"output\": \" Yes, Fe72.5P10C17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr59.81Ni25.31P14.88\\n\",\n        \"output\": \" Yes, Cr59.81Ni25.31P14.88 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Cu2\\n\",\n        \"output\": \" Yes, Ti3Cu2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YAl17Ni2\\n\",\n        \"output\": \" Yes, YAl17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si4BMo15\\n\",\n        \"output\": \" No, Si4BMo15 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4Al\\n\",\n        \"output\": \" No, Zr4Al does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu38.75Ag38.75Ge22.5\\n\",\n        \"output\": \" Yes, Cu38.75Ag38.75Ge22.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni40B3P7\\n\",\n        \"output\": \" Yes, Ni40B3P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaAl17Ni7\\n\",\n        \"output\": \" Yes, LaAl17Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Al16Ni\\n\",\n        \"output\": \" No, La3Al16Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al2Fe43B5\\n\",\n        \"output\": \" No, Al2Fe43B5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn74(SiP)13\\n\",\n        \"output\": \" Yes, Mn74(SiP)13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr2Fe22B\\n\",\n        \"output\": \" Yes, Cr2Fe22B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La7.5Nb7.5Al85\\n\",\n        \"output\": \" Yes, La7.5Nb7.5Al85 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce5Al2Cu43\\n\",\n        \"output\": \" No, Ce5Al2Cu43 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe3Ni5P2\\n\",\n        \"output\": \" Yes, Fe3Ni5P2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr6Co15C4\\n\",\n        \"output\": \" No, Cr6Co15C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd4Mg13Cu3\\n\",\n        \"output\": \" Yes, Nd4Mg13Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10Ti3Si7\\n\",\n        \"output\": \" Yes, Zr10Ti3Si7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe82.5P10C7.5\\n\",\n        \"output\": \" No, Fe82.5P10C7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8Co31B11\\n\",\n        \"output\": \" Yes, Al8Co31B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" larch\\n\",\n        \"output\": \" larch is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni35B13C2\\n\",\n        \"output\": \" No, Ni35B13C2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V7Fe76P17\\n\",\n        \"output\": \" Yes, V7Fe76P17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11.2Co78Mo10.8\\n\",\n        \"output\": \" Yes, Zr11.2Co78Mo10.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu85.5Ag7.5P7\\n\",\n        \"output\": \" Yes, Cu85.5Ag7.5P7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr14.5Co65.5Mo20\\n\",\n        \"output\": \" Yes, Zr14.5Co65.5Mo20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe70Si12.5B17.5\\n\",\n        \"output\": \" Yes, Fe70Si12.5B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al21(FeNi)2\\n\",\n        \"output\": \" Yes, Al21(FeNi)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe7WC2\\n\",\n        \"output\": \" No, Fe7WC2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn7Si20Pd73\\n\",\n        \"output\": \" Yes, Mn7Si20Pd73 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" BMo9\\n\",\n        \"output\": \" No, BMo9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr45Co54Pd\\n\",\n        \"output\": \" Yes, Zr45Co54Pd has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaMg11Cu8\\n\",\n        \"output\": \" Yes, LaMg11Cu8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11Al5Ni4\\n\",\n        \"output\": \" Yes, Zr11Al5Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb20Si4C\\n\",\n        \"output\": \" Yes, Nb20Si4C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn8Co12B5\\n\",\n        \"output\": \" Yes, Mn8Co12B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf9Cu8Ni3\\n\",\n        \"output\": \" Yes, Hf9Cu8Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3VNi6\\n\",\n        \"output\": \" Yes, Zr3VNi6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr2Fe21B2\\n\",\n        \"output\": \" Yes, Cr2Fe21B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe46.2Ni30.8B23\\n\",\n        \"output\": \" Yes, Fe46.2Ni30.8B23 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti6Al3Cu\\n\",\n        \"output\": \" No, Ti6Al3Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn7Al33Si10\\n\",\n        \"output\": \" Yes, Mn7Al33Si10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg35(Zn4Sn)3\\n\",\n        \"output\": \" Yes, Mg35(Zn4Sn)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr14(MnAl)3\\n\",\n        \"output\": \" Yes, Zr14(MnAl)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf19(TaFe8)9\\n\",\n        \"output\": \" Yes, Hf19(TaFe8)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn11Co25B14\\n\",\n        \"output\": \" Yes, Mn11Co25B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti7Al11Cu2\\n\",\n        \"output\": \" No, Ti7Al11Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd8(Fe13B)3\\n\",\n        \"output\": \" No, Nd8(Fe13B)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAl40Ni9\\n\",\n        \"output\": \" Yes, LaAl40Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MgCu\\n\",\n        \"output\": \" No, MgCu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf7.6Zr68.4Fe24\\n\",\n        \"output\": \" Yes, Hf7.6Zr68.4Fe24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu4Si16.9Pd79.1\\n\",\n        \"output\": \" Yes, Cu4Si16.9Pd79.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2(Al15Ni)3\\n\",\n        \"output\": \" No, Mn2(Al15Ni)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd6Mg9Ni5\\n\",\n        \"output\": \" Yes, Nd6Mg9Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd8Al85Ni7\\n\",\n        \"output\": \" Yes, Gd8Al85Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7.8Co90.2W2\\n\",\n        \"output\": \" Yes, Zr7.8Co90.2W2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al7Fe2Ni\\n\",\n        \"output\": \" Yes, Al7Fe2Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni14B7C4\\n\",\n        \"output\": \" Yes, Ni14B7C4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr38Ni37Mo25\\n\",\n        \"output\": \" Yes, Cr38Ni37Mo25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3Cu3Ni4\\n\",\n        \"output\": \" No, Ti3Cu3Ni4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni47Mo53\\n\",\n        \"output\": \" Yes, Ni47Mo53 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" MnAl3Si\\n\",\n        \"output\": \" No, MnAl3Si does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr20Ni61P19\\n\",\n        \"output\": \" Yes, Cr20Ni61P19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe71Cu15B14\\n\",\n        \"output\": \" No, Fe71Cu15B14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Al3Cu4\\n\",\n        \"output\": \" Yes, La3Al3Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe29Cu71\\n\",\n        \"output\": \" No, Fe29Cu71 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd5(Al14Ni)3\\n\",\n        \"output\": \" Yes, Nd5(Al14Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al15Co2\\n\",\n        \"output\": \" No, Ce3Al15Co2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" throne\\n\",\n        \"output\": \" throne is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" adult\\n\",\n        \"output\": \" adult is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn(Ge2Pd9)9\\n\",\n        \"output\": \" Yes, Mn(Ge2Pd9)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Gd9.1Al81.8Fe9.1\\n\",\n        \"output\": \" Yes, Gd9.1Al81.8Fe9.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr10Fe31B9\\n\",\n        \"output\": \" Yes, Cr10Fe31B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd3Al4Cu43\\n\",\n        \"output\": \" No, Nd3Al4Cu43 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si4B11Mo35\\n\",\n        \"output\": \" Yes, Si4B11Mo35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn43(Co15B4)3\\n\",\n        \"output\": \" Yes, Mn43(Co15B4)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Fe43Co2\\n\",\n        \"output\": \" Yes, Zr5Fe43Co2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdMg17Ni2\\n\",\n        \"output\": \" Yes, NdMg17Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4Mg5Ni\\n\",\n        \"output\": \" Yes, La4Mg5Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe80B11P9\\n\",\n        \"output\": \" Yes, Fe80B11P9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9Ta8Si3\\n\",\n        \"output\": \" Yes, Zr9Ta8Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5(Fe9C)2\\n\",\n        \"output\": \" No, Cr5(Fe9C)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al15Cr4Si\\n\",\n        \"output\": \" No, Al15Cr4Si does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CrFe19P5\\n\",\n        \"output\": \" Yes, CrFe19P5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" HfCuNi3\\n\",\n        \"output\": \" Yes, HfCuNi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al47CoNi2\\n\",\n        \"output\": \" No, Al47CoNi2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni73B22C5\\n\",\n        \"output\": \" No, Ni73B22C5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co37Mo4C9\\n\",\n        \"output\": \" No, Co37Mo4C9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni70.5B17Mo12.5\\n\",\n        \"output\": \" Yes, Ni70.5B17Mo12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si2Ni17B6\\n\",\n        \"output\": \" Yes, Si2Ni17B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Pd81.8Rh1.7\\n\",\n        \"output\": \" Yes, Si16.5Pd81.8Rh1.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10Fe89.982Si0.018\\n\",\n        \"output\": \" Yes, Zr10Fe89.982Si0.018 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10AlNi9\\n\",\n        \"output\": \" Yes, Zr10AlNi9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe41Ni42B17\\n\",\n        \"output\": \" Yes, Fe41Ni42B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SiBMo18\\n\",\n        \"output\": \" No, SiBMo18 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15V2Ge3\\n\",\n        \"output\": \" Yes, Zr15V2Ge3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn3Fe93B4\\n\",\n        \"output\": \" No, Mn3Fe93B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7.5Fe83B9.5\\n\",\n        \"output\": \" No, Nb7.5Fe83B9.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si12.5B17.5Mo70\\n\",\n        \"output\": \" Yes, Si12.5B17.5Mo70 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ca2Al17Co\\n\",\n        \"output\": \" Yes, Ca2Al17Co has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Fe44B\\n\",\n        \"output\": \" Yes, Zr5Fe44B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr12Fe85B3\\n\",\n        \"output\": \" Yes, Zr12Fe85B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr16(Co11B)7\\n\",\n        \"output\": \" Yes, Zr16(Co11B)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11(Cu2Ni)3\\n\",\n        \"output\": \" Yes, Zr11(Cu2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiAlCu3\\n\",\n        \"output\": \" Yes, TiAlCu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al2Ni13\\n\",\n        \"output\": \" No, La5Al2Ni13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl16Co3\\n\",\n        \"output\": \" Yes, CeAl16Co3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al14CrSi5\\n\",\n        \"output\": \" No, Al14CrSi5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y2Mg13Ni5\\n\",\n        \"output\": \" Yes, Y2Mg13Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu7Si20Pd73\\n\",\n        \"output\": \" Yes, Cu7Si20Pd73 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Cr6Co41\\n\",\n        \"output\": \" Yes, Zr3Cr6Co41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" fork\\n\",\n        \"output\": \" fork is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" TiNb16Si3\\n\",\n        \"output\": \" Yes, TiNb16Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co37W7C6\\n\",\n        \"output\": \" No, Co37W7C6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe75P17.5C7.5\\n\",\n        \"output\": \" Yes, Fe75P17.5C7.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni29B20C\\n\",\n        \"output\": \" Yes, Ni29B20C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al14(CrSi)3\\n\",\n        \"output\": \" No, Al14(CrSi)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2Mg17Ag\\n\",\n        \"output\": \" No, Y2Mg17Ag does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" rabbi\\n\",\n        \"output\": \" rabbi is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti4Ni\\n\",\n        \"output\": \" No, Ti4Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5(Nb4Si)3\\n\",\n        \"output\": \" Yes, Zr5(Nb4Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y2Mg5Cu3\\n\",\n        \"output\": \" Yes, Y2Mg5Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe29Co54B17\\n\",\n        \"output\": \" Yes, Fe29Co54B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" SiNi19\\n\",\n        \"output\": \" No, SiNi19 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Al5Cu43\\n\",\n        \"output\": \" No, Nd2Al5Cu43 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd(Al8Ni)11\\n\",\n        \"output\": \" Yes, Nd(Al8Ni)11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce2Mn5Al93\\n\",\n        \"output\": \" No, Ce2Mn5Al93 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti2Cu3\\n\",\n        \"output\": \" Yes, Ti2Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al4Ni\\n\",\n        \"output\": \" Yes, La5Al4Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdAl8Ni\\n\",\n        \"output\": \" Yes, NdAl8Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu5(Ni4P)9\\n\",\n        \"output\": \" Yes, Cu5(Ni4P)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La11Al8Ni\\n\",\n        \"output\": \" Yes, La11Al8Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr6.5Cr16Co77.5\\n\",\n        \"output\": \" Yes, Zr6.5Cr16Co77.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La15Al3Ni32\\n\",\n        \"output\": \" Yes, La15Al3Ni32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9AlNi15\\n\",\n        \"output\": \" Yes, La9AlNi15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeCu11Ag8\\n\",\n        \"output\": \" Yes, CeCu11Ag8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni23B25C2\\n\",\n        \"output\": \" No, Ni23B25C2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" GdAl8Ni\\n\",\n        \"output\": \" Yes, GdAl8Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe74Mo9P17\\n\",\n        \"output\": \" Yes, Fe74Mo9P17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5Fe17B3\\n\",\n        \"output\": \" Yes, Cr5Fe17B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3CoB\\n\",\n        \"output\": \" Yes, Mn3CoB has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3Al7\\n\",\n        \"output\": \" No, Ti3Al7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15Ti3Si2\\n\",\n        \"output\": \" Yes, Zr15Ti3Si2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La5Al7Ni8\\n\",\n        \"output\": \" Yes, La5Al7Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Yb28.42Ce20.56Cu51.02\\n\",\n        \"output\": \" Yes, Yb28.42Ce20.56Cu51.02 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al5Si3\\n\",\n        \"output\": \" Yes, Mn2Al5Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" professor\\n\",\n        \"output\": \" professor is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn7.5Co67.5B25\\n\",\n        \"output\": \" Yes, Mn7.5Co67.5B25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Pd76.8Rh6.7\\n\",\n        \"output\": \" No, Si16.5Pd76.8Rh6.7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe53Ni30B17\\n\",\n        \"output\": \" Yes, Fe53Ni30B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu5.7Si20.5Pd73.8\\n\",\n        \"output\": \" Yes, Cu5.7Si20.5Pd73.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Fe85B12\\n\",\n        \"output\": \" No, Mn3Fe85B12 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7.5Co79.5W13\\n\",\n        \"output\": \" Yes, Zr7.5Co79.5W13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La5Mg3Cu2\\n\",\n        \"output\": \" No, La5Mg3Cu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr10Co11C4\\n\",\n        \"output\": \" No, Cr10Co11C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ba4.5La68Cu27.5\\n\",\n        \"output\": \" Yes, Ba4.5La68Cu27.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd4Mg11Ni5\\n\",\n        \"output\": \" Yes, Nd4Mg11Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co39Si5B6\\n\",\n        \"output\": \" Yes, Co39Si5B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10V0.018Fe89.982\\n\",\n        \"output\": \" Yes, Zr10V0.018Fe89.982 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni27B23\\n\",\n        \"output\": \" No, Ni27B23 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAl15Co4\\n\",\n        \"output\": \" No, CeAl15Co4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrNi9\\n\",\n        \"output\": \" Yes, ZrNi9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si2Ni17C\\n\",\n        \"output\": \" No, Si2Ni17C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2AlNi17\\n\",\n        \"output\": \" Yes, Zr2AlNi17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf48Nb37Si15\\n\",\n        \"output\": \" Yes, Hf48Nb37Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al6Co25B19\\n\",\n        \"output\": \" Yes, Al6Co25B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg16Al27Pd7\\n\",\n        \"output\": \" No, Mg16Al27Pd7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr7Fe38B5\\n\",\n        \"output\": \" No, Cr7Fe38B5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La16Al3Ni\\n\",\n        \"output\": \" Yes, La16Al3Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4Co20W\\n\",\n        \"output\": \" Yes, Zr4Co20W has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co17Si3\\n\",\n        \"output\": \" No, Co17Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb15Si2Ge3\\n\",\n        \"output\": \" Yes, Nb15Si2Ge3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al14Ni5Mo\\n\",\n        \"output\": \" Yes, Al14Ni5Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al17CoNi2\\n\",\n        \"output\": \" No, Al17CoNi2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si3(Ni10B)2\\n\",\n        \"output\": \" No, Si3(Ni10B)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr14(TiSi)3\\n\",\n        \"output\": \" Yes, Zr14(TiSi)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al24Cr\\n\",\n        \"output\": \" No, Al24Cr does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La5Al3Ni2\\n\",\n        \"output\": \" Yes, La5Al3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrTi5Be4\\n\",\n        \"output\": \" Yes, ZrTi5Be4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si4Ni17B4\\n\",\n        \"output\": \" No, Si4Ni17B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe30B19F\\n\",\n        \"output\": \" Yes, Fe30B19F has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni41.5P17Pd41.5\\n\",\n        \"output\": \" Yes, Ni41.5P17Pd41.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca7Mg2Cu\\n\",\n        \"output\": \" Yes, Ca7Mg2Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La34Al53Ni13\\n\",\n        \"output\": \" Yes, La34Al53Ni13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb10.3Fe80.3B9.4\\n\",\n        \"output\": \" Yes, Nb10.3Fe80.3B9.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe33B7Mo10\\n\",\n        \"output\": \" Yes, Fe33B7Mo10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe67(Ni5B6)3\\n\",\n        \"output\": \" Yes, Fe67(Ni5B6)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr16AlNi33\\n\",\n        \"output\": \" Yes, Zr16AlNi33 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Fe41B4\\n\",\n        \"output\": \" Yes, Zr5Fe41B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf72Nb13Si15\\n\",\n        \"output\": \" Yes, Hf72Nb13Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti16Al19Ni15\\n\",\n        \"output\": \" Yes, Ti16Al19Ni15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaZr5Fe44\\n\",\n        \"output\": \" Yes, LaZr5Fe44 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y(Mg2Ni)3\\n\",\n        \"output\": \" Yes, Y(Mg2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe82.5P12.5C5\\n\",\n        \"output\": \" No, Fe82.5P12.5C5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr28Al15Ni7\\n\",\n        \"output\": \" Yes, Zr28Al15Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La7Al91Ni2\\n\",\n        \"output\": \" Yes, La7Al91Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd(Al11Ni)2\\n\",\n        \"output\": \" Yes, Nd(Al11Ni)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3Co41W6\\n\",\n        \"output\": \" Yes, Zr3Co41W6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd3Al47\\n\",\n        \"output\": \" No, Gd3Al47 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd7Mg9Ni4\\n\",\n        \"output\": \" Yes, Nd7Mg9Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La16Al3Ni31\\n\",\n        \"output\": \" Yes, La16Al3Ni31 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Al41Ni6\\n\",\n        \"output\": \" Yes, Nd3Al41Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn3Al16Ni\\n\",\n        \"output\": \" No, Mn3Al16Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al2Co31B17\\n\",\n        \"output\": \" Yes, Al2Co31B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr60.3Fe10Ni29.7\\n\",\n        \"output\": \" Yes, Zr60.3Fe10Ni29.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al17Cu\\n\",\n        \"output\": \" Yes, Ce2Al17Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe51Cu38Ag11\\n\",\n        \"output\": \" No, Fe51Cu38Ag11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al87.5Fe0.5Ni12\\n\",\n        \"output\": \" Yes, Al87.5Fe0.5Ni12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni8P5Pt12\\n\",\n        \"output\": \" No, Ni8P5Pt12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr8Co37B5\\n\",\n        \"output\": \" Yes, Zr8Co37B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co62.5Si12.5B25\\n\",\n        \"output\": \" Yes, Co62.5Si12.5B25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CaAl18Fe\\n\",\n        \"output\": \" No, CaAl18Fe does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Fe76.5Ni13.5\\n\",\n        \"output\": \" Yes, Zr10Fe76.5Ni13.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe13Si3C4\\n\",\n        \"output\": \" Yes, Fe13Si3C4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y15Mg83Mn2\\n\",\n        \"output\": \" No, Y15Mg83Mn2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" V10Co76.5B13.5\\n\",\n        \"output\": \" Yes, V10Co76.5B13.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La4Al\\n\",\n        \"output\": \" Yes, La4Al has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni36B13C\\n\",\n        \"output\": \" No, Ni36B13C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" cactus\\n\",\n        \"output\": \" cactus is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe4Ag21\\n\",\n        \"output\": \" No, Fe4Ag21 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" FeCo15B4\\n\",\n        \"output\": \" Yes, FeCo15B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al42Fe3Ni5\\n\",\n        \"output\": \" No, Al42Fe3Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Al11Ni6\\n\",\n        \"output\": \" No, Zr3Al11Ni6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg17Ni3\\n\",\n        \"output\": \" Yes, Mg17Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La4Al5Ni\\n\",\n        \"output\": \" Yes, La4Al5Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Sr10La53Cu37\\n\",\n        \"output\": \" Yes, Sr10La53Cu37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V5(Fe14B)3\\n\",\n        \"output\": \" No, V5(Fe14B)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5CrFe44\\n\",\n        \"output\": \" Yes, Zr5CrFe44 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" pyjama\\n\",\n        \"output\": \" pyjama is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti26Al57Ni17\\n\",\n        \"output\": \" Yes, Ti26Al57Ni17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni55B42.5C2.5\\n\",\n        \"output\": \" No, Ni55B42.5C2.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2(FeCo)9\\n\",\n        \"output\": \" Yes, Zr2(FeCo)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al23CoNi\\n\",\n        \"output\": \" No, Al23CoNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni43P14Pd43\\n\",\n        \"output\": \" Yes, Ni43P14Pd43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si10B17Mo73\\n\",\n        \"output\": \" Yes, Si10B17Mo73 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y21Al15Cu14\\n\",\n        \"output\": \" Yes, Y21Al15Cu14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd3Al13Cu4\\n\",\n        \"output\": \" Yes, Gd3Al13Cu4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co5Ni74P21\\n\",\n        \"output\": \" Yes, Co5Ni74P21 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr7Co13C5\\n\",\n        \"output\": \" Yes, Cr7Co13C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La4Mg11Ni5\\n\",\n        \"output\": \" Yes, La4Mg11Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn17.4Al76.6Si6\\n\",\n        \"output\": \" No, Mn17.4Al76.6Si6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr47.5Cu50B2.5\\n\",\n        \"output\": \" Yes, Zr47.5Cu50B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Cu37Ag10\\n\",\n        \"output\": \" Yes, Ce3Cu37Ag10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe65Si12.5C22.5\\n\",\n        \"output\": \" Yes, Fe65Si12.5C22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" LaMg3Ni\\n\",\n        \"output\": \" Yes, LaMg3Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu69Ni13P18\\n\",\n        \"output\": \" Yes, Cu69Ni13P18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81B4Mo15\\n\",\n        \"output\": \" No, Fe81B4Mo15 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" taste\\n\",\n        \"output\": \" taste is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NdNi\\n\",\n        \"output\": \" No, NdNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Mg12Ni5\\n\",\n        \"output\": \" Yes, La3Mg12Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn10Co8B7\\n\",\n        \"output\": \" Yes, Mn10Co8B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6Al3Ni11\\n\",\n        \"output\": \" Yes, Zr6Al3Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr13Co26C11\\n\",\n        \"output\": \" No, Cr13Co26C11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co16SiB3\\n\",\n        \"output\": \" Yes, Co16SiB3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr56.95Cr15Ni28.05\\n\",\n        \"output\": \" Yes, Zr56.95Cr15Ni28.05 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y27Al5Cu18\\n\",\n        \"output\": \" Yes, Y27Al5Cu18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co38Mo5C7\\n\",\n        \"output\": \" No, Co38Mo5C7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Cu3Ni2\\n\",\n        \"output\": \" Yes, Zr5Cu3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb11V5Si4\\n\",\n        \"output\": \" No, Nb11V5Si4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y5Mg3Ag2\\n\",\n        \"output\": \" Yes, Y5Mg3Ag2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr35Ni27Mo38\\n\",\n        \"output\": \" Yes, Cr35Ni27Mo38 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce4Mg13Cu3\\n\",\n        \"output\": \" No, Ce4Mg13Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe79Cu5B16\\n\",\n        \"output\": \" No, Fe79Cu5B16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Fe34B11\\n\",\n        \"output\": \" Yes, Zr5Fe34B11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr15Fe71B14\\n\",\n        \"output\": \" Yes, Cr15Fe71B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd8.2Al83.6Fe8.2\\n\",\n        \"output\": \" Yes, Gd8.2Al83.6Fe8.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe8SiB\\n\",\n        \"output\": \" Yes, Fe8SiB has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y2Al7Ni\\n\",\n        \"output\": \" No, Y2Al7Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sm2(Al5Ni)3\\n\",\n        \"output\": \" Yes, Sm2(Al5Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81.5Cu1.5B17\\n\",\n        \"output\": \" Yes, Fe81.5Cu1.5B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn27Co45B28\\n\",\n        \"output\": \" Yes, Mn27Co45B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf11(CuNi2)3\\n\",\n        \"output\": \" Yes, Hf11(CuNi2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10Al0.054Fe89.946\\n\",\n        \"output\": \" Yes, Zr10Al0.054Fe89.946 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al46Fe3Co\\n\",\n        \"output\": \" No, Al46Fe3Co does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" BMo4\\n\",\n        \"output\": \" No, BMo4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb11.5Ni71.5B17\\n\",\n        \"output\": \" Yes, Nb11.5Ni71.5B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti14(SiNi)3\\n\",\n        \"output\": \" Yes, Ti14(SiNi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2(NbCo5)3\\n\",\n        \"output\": \" Yes, Mn2(NbCo5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ta4Ti13Si3\\n\",\n        \"output\": \" Yes, Ta4Ti13Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiNi\\n\",\n        \"output\": \" No, TiNi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu9Si16Pd75\\n\",\n        \"output\": \" Yes, Cu9Si16Pd75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti17Al35Ni48\\n\",\n        \"output\": \" Yes, Ti17Al35Ni48 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni24B19C7\\n\",\n        \"output\": \" Yes, Ni24B19C7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe20BF4\\n\",\n        \"output\": \" No, Fe20BF4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti42(AlNi)29\\n\",\n        \"output\": \" Yes, Ti42(AlNi)29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe81Ni3B16\\n\",\n        \"output\": \" Yes, Fe81Ni3B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd7Mg9Cu4\\n\",\n        \"output\": \" Yes, Nd7Mg9Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe28B9F13\\n\",\n        \"output\": \" No, Fe28B9F13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si5Pd19Au\\n\",\n        \"output\": \" Yes, Si5Pd19Au has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" enemy\\n\",\n        \"output\": \" enemy is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn30.5Co41.5B28\\n\",\n        \"output\": \" Yes, Mn30.5Co41.5B28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y7.5Mg82.5Mn10\\n\",\n        \"output\": \" No, Y7.5Mg82.5Mn10 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2(Al5Fe)3\\n\",\n        \"output\": \" No, Ce2(Al5Fe)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr16Al3Ni\\n\",\n        \"output\": \" Yes, Zr16Al3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La6Al3Ni11\\n\",\n        \"output\": \" Yes, La6Al3Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni16BC3\\n\",\n        \"output\": \" No, Ni16BC3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti7AlCu2\\n\",\n        \"output\": \" No, Ti7AlCu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg9Ni\\n\",\n        \"output\": \" Yes, Mg9Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr27.5Cu70B2.5\\n\",\n        \"output\": \" Yes, Zr27.5Cu70B2.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al47FeNi2\\n\",\n        \"output\": \" No, Al47FeNi2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CaMg18Cu\\n\",\n        \"output\": \" No, CaMg18Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Cu67Ag30\\n\",\n        \"output\": \" No, Ce3Cu67Ag30 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe15Si16.5Pd68.5\\n\",\n        \"output\": \" No, Fe15Si16.5Pd68.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr40Al9Ni\\n\",\n        \"output\": \" Yes, Zr40Al9Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe7Si2B\\n\",\n        \"output\": \" Yes, Fe7Si2B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15Cu4Ni\\n\",\n        \"output\": \" No, Zr15Cu4Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrAl3Ni\\n\",\n        \"output\": \" Yes, ZrAl3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" SiPd4\\n\",\n        \"output\": \" Yes, SiPd4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" ZrFeCo8\\n\",\n        \"output\": \" Yes, ZrFeCo8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf25Zr32Be43\\n\",\n        \"output\": \" Yes, Hf25Zr32Be43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu84.5Ag7P8.5\\n\",\n        \"output\": \" No, Cu84.5Ag7P8.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15Ti2Si3\\n\",\n        \"output\": \" Yes, Zr15Ti2Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg11Ti25Al14\\n\",\n        \"output\": \" Yes, Mg11Ti25Al14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr17La48Cu35\\n\",\n        \"output\": \" Yes, Sr17La48Cu35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg7Cu3\\n\",\n        \"output\": \" Yes, Mg7Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrCr2Fe7\\n\",\n        \"output\": \" Yes, ZrCr2Fe7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf2Ta7Fe16\\n\",\n        \"output\": \" Yes, Hf2Ta7Fe16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2AlCu2\\n\",\n        \"output\": \" Yes, La2AlCu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn4Al11Si5\\n\",\n        \"output\": \" Yes, Mn4Al11Si5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Cu4Ni3\\n\",\n        \"output\": \" Yes, Zr3Cu4Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al12V3Ge5\\n\",\n        \"output\": \" Yes, Al12V3Ge5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn17(Co7B4)3\\n\",\n        \"output\": \" Yes, Mn17(Co7B4)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce4Mg15Cu\\n\",\n        \"output\": \" No, Ce4Mg15Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Al2Ni3\\n\",\n        \"output\": \" Yes, Zr5Al2Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd4.5Fe77B18.5\\n\",\n        \"output\": \" Yes, Nd4.5Fe77B18.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La3Mg14Cu3\\n\",\n        \"output\": \" No, La3Mg14Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd5.5Al89Fe5.5\\n\",\n        \"output\": \" Yes, Gd5.5Al89Fe5.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe36Cu13Ag51\\n\",\n        \"output\": \" No, Fe36Cu13Ag51 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al2Co7B\\n\",\n        \"output\": \" No, Al2Co7B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni81.5B5.5P13\\n\",\n        \"output\": \" Yes, Ni81.5B5.5P13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg14(AlZn)3\\n\",\n        \"output\": \" No, Mg14(AlZn)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe33W6C11\\n\",\n        \"output\": \" Yes, Fe33W6C11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAlCu3\\n\",\n        \"output\": \" No, LaAlCu3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr67.5Cu30B2.5\\n\",\n        \"output\": \" Yes, Zr67.5Cu30B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si18Ni16.4Pd65.6\\n\",\n        \"output\": \" Yes, Si18Ni16.4Pd65.6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu14.4Ni65.6P20\\n\",\n        \"output\": \" Yes, Cu14.4Ni65.6P20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Nb11Si4\\n\",\n        \"output\": \" Yes, Zr5Nb11Si4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn12Nb15Co73\\n\",\n        \"output\": \" Yes, Mn12Nb15Co73 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5(Co14W)3\\n\",\n        \"output\": \" Yes, Zr5(Co14W)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co2Ni78.5P19.5\\n\",\n        \"output\": \" Yes, Co2Ni78.5P19.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al27Mo23\\n\",\n        \"output\": \" Yes, Al27Mo23 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe24Ni59B17\\n\",\n        \"output\": \" Yes, Fe24Ni59B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe75B11P14\\n\",\n        \"output\": \" No, Fe75B11P14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al18FeNi\\n\",\n        \"output\": \" No, Al18FeNi does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Al5Cu41\\n\",\n        \"output\": \" Yes, Nd4Al5Cu41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr7Fe35B8\\n\",\n        \"output\": \" Yes, Cr7Fe35B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti23Al40Ni37\\n\",\n        \"output\": \" Yes, Ti23Al40Ni37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" helen\\n\",\n        \"output\": \" helen is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Tb30(Fe9Co)7\\n\",\n        \"output\": \" Yes, Tb30(Fe9Co)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8TiSi\\n\",\n        \"output\": \" Yes, Zr8TiSi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti12V5Si3\\n\",\n        \"output\": \" Yes, Ti12V5Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe79.5Cu0.5B20\\n\",\n        \"output\": \" Yes, Fe79.5Cu0.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La6Al11Ni3\\n\",\n        \"output\": \" No, La6Al11Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Ni\\n\",\n        \"output\": \" No, Ti9Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg6AlZn3\\n\",\n        \"output\": \" No, Mg6AlZn3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" SiNi19B5\\n\",\n        \"output\": \" Yes, SiNi19B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co12.5Ni68.5P19\\n\",\n        \"output\": \" No, Co12.5Ni68.5P19 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al12Cr5Si3\\n\",\n        \"output\": \" No, Al12Cr5Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni70.5B17W12.5\\n\",\n        \"output\": \" Yes, Ni70.5B17W12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr8.3Cr8.3Co83.4\\n\",\n        \"output\": \" Yes, Zr8.3Cr8.3Co83.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Pd68.5Au15\\n\",\n        \"output\": \" Yes, Si16.5Pd68.5Au15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La9Al13Ni28\\n\",\n        \"output\": \" Yes, La9Al13Ni28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn59Co25B16\\n\",\n        \"output\": \" Yes, Mn59Co25B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd2(Al5Ni)3\\n\",\n        \"output\": \" Yes, Nd2(Al5Ni)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe15NiB4\\n\",\n        \"output\": \" Yes, Fe15NiB4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr16.5Co77.5Mo6\\n\",\n        \"output\": \" Yes, Zr16.5Co77.5Mo6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu82.5Ag9P8.5\\n\",\n        \"output\": \" No, Cu82.5Ag9P8.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti42Al51Ni7\\n\",\n        \"output\": \" Yes, Ti42Al51Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr11Al5Co4\\n\",\n        \"output\": \" Yes, Zr11Al5Co4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiCu7Ni2\\n\",\n        \"output\": \" No, TiCu7Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr7Fe77B16\\n\",\n        \"output\": \" Yes, Cr7Fe77B16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr24Ni11Mo15\\n\",\n        \"output\": \" Yes, Cr24Ni11Mo15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La0.3Zr10Fe89.7\\n\",\n        \"output\": \" Yes, La0.3Zr10Fe89.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10(Fe9Ni)9\\n\",\n        \"output\": \" Yes, Zr10(Fe9Ni)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La87Al13\\n\",\n        \"output\": \" Yes, La87Al13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr30Ni19B\\n\",\n        \"output\": \" Yes, Zr30Ni19B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YMg19\\n\",\n        \"output\": \" No, YMg19 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba7La51.5Cu41.5\\n\",\n        \"output\": \" Yes, Ba7La51.5Cu41.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce11Al89\\n\",\n        \"output\": \" Yes, Ce11Al89 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La9Al24Ni17\\n\",\n        \"output\": \" Yes, La9Al24Ni17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe43B6N\\n\",\n        \"output\": \" Yes, Fe43B6N has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe70(Si3B7)3\\n\",\n        \"output\": \" Yes, Fe70(Si3B7)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al22Co3\\n\",\n        \"output\": \" No, Al22Co3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La10Al14Ni\\n\",\n        \"output\": \" Yes, La10Al14Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6AlNi3\\n\",\n        \"output\": \" Yes, Zr6AlNi3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" manicure\\n\",\n        \"output\": \" manicure is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg5Ti19Al26\\n\",\n        \"output\": \" Yes, Mg5Ti19Al26 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe17P2C\\n\",\n        \"output\": \" No, Fe17P2C does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10Fe89.91Si0.09\\n\",\n        \"output\": \" Yes, Zr10Fe89.91Si0.09 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe86(BC)7\\n\",\n        \"output\": \" Yes, Fe86(BC)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe43Ni43B14\\n\",\n        \"output\": \" Yes, Fe43Ni43B14 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti10Be7Si3\\n\",\n        \"output\": \" No, Ti10Be7Si3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf9Nb8Si3\\n\",\n        \"output\": \" Yes, Hf9Nb8Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La22Al19Ni59\\n\",\n        \"output\": \" Yes, La22Al19Ni59 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9.2V9Co81.8\\n\",\n        \"output\": \" Yes, Zr9.2V9Co81.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti2AlCu\\n\",\n        \"output\": \" No, Ti2AlCu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf52(Nb11Si5)3\\n\",\n        \"output\": \" Yes, Hf52(Nb11Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaMg7Zn2\\n\",\n        \"output\": \" Yes, LaMg7Zn2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si10Ge7Pd83\\n\",\n        \"output\": \" Yes, Si10Ge7Pd83 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb15Si4W\\n\",\n        \"output\": \" Yes, Nb15Si4W has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe14Cu55Ag31\\n\",\n        \"output\": \" No, Fe14Cu55Ag31 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8Ni23B19\\n\",\n        \"output\": \" Yes, Al8Ni23B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf11Cu5Ni4\\n\",\n        \"output\": \" Yes, Hf11Cu5Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr63.65Cr5Ni31.35\\n\",\n        \"output\": \" Yes, Zr63.65Cr5Ni31.35 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Al8Ni9\\n\",\n        \"output\": \" No, La3Al8Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al4Ni\\n\",\n        \"output\": \" No, Al4Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87Fe4Co9\\n\",\n        \"output\": \" No, Al87Fe4Co9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2Mg7Cu\\n\",\n        \"output\": \" Yes, Nd2Mg7Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni11P2Pd7\\n\",\n        \"output\": \" Yes, Ni11P2Pd7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce2Al22V\\n\",\n        \"output\": \" No, Ce2Al22V does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe89B6Mo5\\n\",\n        \"output\": \" No, Fe89B6Mo5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu12Ni67P21\\n\",\n        \"output\": \" No, Cu12Ni67P21 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SiNi16C3\\n\",\n        \"output\": \" No, SiNi16C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" magician\\n\",\n        \"output\": \" magician is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3Cu17\\n\",\n        \"output\": \" No, Ti3Cu17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6.5V14Co79.5\\n\",\n        \"output\": \" Yes, Zr6.5V14Co79.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y5Mg44Mn\\n\",\n        \"output\": \" Yes, Y5Mg44Mn has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" soccer\\n\",\n        \"output\": \" soccer is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si8(Ni5B)7\\n\",\n        \"output\": \" Yes, Si8(Ni5B)7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe23Ni59B18\\n\",\n        \"output\": \" Yes, Fe23Ni59B18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" B15(Mo3Ru2)17\\n\",\n        \"output\": \" Yes, B15(Mo3Ru2)17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn5Co13B7\\n\",\n        \"output\": \" Yes, Mn5Co13B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al10Co21B19\\n\",\n        \"output\": \" Yes, Al10Co21B19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti3Al\\n\",\n        \"output\": \" No, Ti3Al does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr23Ni17Mo10\\n\",\n        \"output\": \" Yes, Cr23Ni17Mo10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrTi2Si7\\n\",\n        \"output\": \" Yes, ZrTi2Si7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn2Al87Ni11\\n\",\n        \"output\": \" Yes, Mn2Al87Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr9Al81Ni10\\n\",\n        \"output\": \" Yes, Zr9Al81Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si7GePd42\\n\",\n        \"output\": \" Yes, Si7GePd42 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeCu59Ag40\\n\",\n        \"output\": \" No, CeCu59Ag40 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg18Ni\\n\",\n        \"output\": \" No, NdMg18Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Al2Cr\\n\",\n        \"output\": \" Yes, Zr7Al2Cr has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" eyebrow\\n\",\n        \"output\": \" eyebrow is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeCu4Ag5\\n\",\n        \"output\": \" Yes, CeCu4Ag5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Gd3Al2\\n\",\n        \"output\": \" Yes, Gd3Al2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr14.5V18Co67.5\\n\",\n        \"output\": \" Yes, Zr14.5V18Co67.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" SmAl16Ni3\\n\",\n        \"output\": \" Yes, SmAl16Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe13B4F3\\n\",\n        \"output\": \" Yes, Fe13B4F3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5P15C7.5\\n\",\n        \"output\": \" Yes, Fe77.5P15C7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu85(Ag3P2)3\\n\",\n        \"output\": \" No, Cu85(Ag3P2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd13Fe79B8\\n\",\n        \"output\": \" Yes, Nd13Fe79B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La7Al43\\n\",\n        \"output\": \" Yes, La7Al43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce4Al41Ni5\\n\",\n        \"output\": \" Yes, Ce4Al41Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y2Mg17Cu\\n\",\n        \"output\": \" Yes, Y2Mg17Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe41.5Ni41B17.5\\n\",\n        \"output\": \" Yes, Fe41.5Ni41B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" windshield\\n\",\n        \"output\": \" windshield is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni3B5C2\\n\",\n        \"output\": \" Yes, Ni3B5C2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe7Ni9P4\\n\",\n        \"output\": \" Yes, Fe7Ni9P4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe54Ni29B17\\n\",\n        \"output\": \" Yes, Fe54Ni29B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn3Al46Co\\n\",\n        \"output\": \" No, Mn3Al46Co does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr5Fe11B4\\n\",\n        \"output\": \" Yes, Cr5Fe11B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15Al3Ni32\\n\",\n        \"output\": \" Yes, Zr15Al3Ni32 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti57Be43\\n\",\n        \"output\": \" No, Ti57Be43 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr5Fe83B12\\n\",\n        \"output\": \" Yes, Cr5Fe83B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co3WC\\n\",\n        \"output\": \" No, Co3WC does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" YMg14Cu5\\n\",\n        \"output\": \" Yes, YMg14Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr19Cu31\\n\",\n        \"output\": \" Yes, Zr19Cu31 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9V2Ni9\\n\",\n        \"output\": \" Yes, Zr9V2Ni9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La2AlCu\\n\",\n        \"output\": \" Yes, La2AlCu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al44(CoNi)3\\n\",\n        \"output\": \" No, Al44(CoNi)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Co17W\\n\",\n        \"output\": \" Yes, Zr2Co17W has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr66.9Co33Ni0.1\\n\",\n        \"output\": \" Yes, Zr66.9Co33Ni0.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si5B11Mo34\\n\",\n        \"output\": \" Yes, Si5B11Mo34 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mg17Al71Pd12\\n\",\n        \"output\": \" Yes, Mg17Al71Pd12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11Ti4Si5\\n\",\n        \"output\": \" Yes, Zr11Ti4Si5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si20Pd73Au7\\n\",\n        \"output\": \" Yes, Si20Pd73Au7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co67.5Si17.5C15\\n\",\n        \"output\": \" Yes, Co67.5Si17.5C15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" chief\\n\",\n        \"output\": \" chief is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr67(Fe7B4)3\\n\",\n        \"output\": \" Yes, Zr67(Fe7B4)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co33B17\\n\",\n        \"output\": \" Yes, Co33B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La3Mg10Ni7\\n\",\n        \"output\": \" Yes, La3Mg10Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" HfNi\\n\",\n        \"output\": \" Yes, HfNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce4NbAl45\\n\",\n        \"output\": \" Yes, Ce4NbAl45 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg22(Al3Pd)7\\n\",\n        \"output\": \" No, Mg22(Al3Pd)7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe16B3P\\n\",\n        \"output\": \" Yes, Fe16B3P has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr5Mn4Fe41\\n\",\n        \"output\": \" Yes, Zr5Mn4Fe41 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al5VCu4\\n\",\n        \"output\": \" No, Al5VCu4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe80Si7.5B12.5\\n\",\n        \"output\": \" Yes, Fe80Si7.5B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni38B11C\\n\",\n        \"output\": \" No, Ni38B11C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" icon\\n\",\n        \"output\": \" icon is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" ZrCo9\\n\",\n        \"output\": \" Yes, ZrCo9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" YAl16Ni3\\n\",\n        \"output\": \" Yes, YAl16Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd4Al3Cu43\\n\",\n        \"output\": \" Yes, Nd4Al3Cu43 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti8Al17\\n\",\n        \"output\": \" Yes, Ti8Al17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni35B7C8\\n\",\n        \"output\": \" No, Ni35B7C8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CrSi5Pd19\\n\",\n        \"output\": \" Yes, CrSi5Pd19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd7Al83Ni10\\n\",\n        \"output\": \" Yes, Nd7Al83Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe20BP4\\n\",\n        \"output\": \" Yes, Fe20BP4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al10Fe27B13\\n\",\n        \"output\": \" Yes, Al10Fe27B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2MgCu2\\n\",\n        \"output\": \" No, La2MgCu2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiAl11Cu8\\n\",\n        \"output\": \" Yes, TiAl11Cu8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti9Cu9Ni2\\n\",\n        \"output\": \" Yes, Ti9Cu9Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr67Fe29.7Ni3.3\\n\",\n        \"output\": \" Yes, Zr67Fe29.7Ni3.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y4Mg13Ni3\\n\",\n        \"output\": \" Yes, Y4Mg13Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr15Nb2Si3\\n\",\n        \"output\": \" Yes, Zr15Nb2Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87Fe4Ni9\\n\",\n        \"output\": \" No, Al87Fe4Ni9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti16SiNi3\\n\",\n        \"output\": \" No, Ti16SiNi3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe67.5Si12.5B20\\n\",\n        \"output\": \" Yes, Fe67.5Si12.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn(Al11Ni)2\\n\",\n        \"output\": \" No, Mn(Al11Ni)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf13.7Fe50.2O36.1\\n\",\n        \"output\": \" Yes, Hf13.7Fe50.2O36.1 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdAl5Cu44\\n\",\n        \"output\": \" No, NdAl5Cu44 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al4Ni27B19\\n\",\n        \"output\": \" Yes, Al4Ni27B19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf51Nb34Si15\\n\",\n        \"output\": \" Yes, Hf51Nb34Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr57Ti8Si35\\n\",\n        \"output\": \" Yes, Zr57Ti8Si35 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Al12Cu\\n\",\n        \"output\": \" No, Ti7Al12Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr53Nb30Si17\\n\",\n        \"output\": \" Yes, Zr53Nb30Si17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg70(Cu7Au3)3\\n\",\n        \"output\": \" Yes, Mg70(Cu7Au3)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr29Al13Ni58\\n\",\n        \"output\": \" Yes, Zr29Al13Ni58 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Sr15.5La51.5Cu33\\n\",\n        \"output\": \" Yes, Sr15.5La51.5Cu33 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe21Ni61.5B17.5\\n\",\n        \"output\": \" Yes, Fe21Ni61.5B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu1.7Si16.5Pd81.8\\n\",\n        \"output\": \" Yes, Cu1.7Si16.5Pd81.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg12Ni5\\n\",\n        \"output\": \" Yes, Nd3Mg12Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe12.5Si16.5Pd71\\n\",\n        \"output\": \" Yes, Fe12.5Si16.5Pd71 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe83B8C9\\n\",\n        \"output\": \" Yes, Fe83B8C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb5Fe89B6\\n\",\n        \"output\": \" No, Nb5Fe89B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti50Cu13Ni37\\n\",\n        \"output\": \" No, Ti50Cu13Ni37 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe60B7F33\\n\",\n        \"output\": \" No, Fe60B7F33 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaAlNi3\\n\",\n        \"output\": \" No, LaAlNi3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" possibility\\n\",\n        \"output\": \" possibility is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn18.5Co65.5B16\\n\",\n        \"output\": \" Yes, Mn18.5Co65.5B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf56V29Si15\\n\",\n        \"output\": \" Yes, Hf56V29Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe40SiB9\\n\",\n        \"output\": \" Yes, Fe40SiB9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe80P13C7\\n\",\n        \"output\": \" Yes, Fe80P13C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr17.5Cu80B2.5\\n\",\n        \"output\": \" Yes, Zr17.5Cu80B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti13Nb4Si3\\n\",\n        \"output\": \" Yes, Ti13Nb4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al87Fe6Ni7\\n\",\n        \"output\": \" No, Al87Fe6Ni7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co72.5Si12.5B15\\n\",\n        \"output\": \" Yes, Co72.5Si12.5B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3(Co8B3)2\\n\",\n        \"output\": \" Yes, Ti3(Co8B3)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La8AlNi11\\n\",\n        \"output\": \" Yes, La8AlNi11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co5Ni73P22\\n\",\n        \"output\": \" No, Co5Ni73P22 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al12Ni29B9\\n\",\n        \"output\": \" No, Al12Ni29B9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr3Fe14B3\\n\",\n        \"output\": \" Yes, Cr3Fe14B3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La41AlNi8\\n\",\n        \"output\": \" Yes, La41AlNi8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al13Fe4\\n\",\n        \"output\": \" No, Ce3Al13Fe4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11Be7Nb2\\n\",\n        \"output\": \" Yes, Zr11Be7Nb2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si15Ni67.5C17.5\\n\",\n        \"output\": \" Yes, Si15Ni67.5C17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al58Cr17Si25\\n\",\n        \"output\": \" Yes, Al58Cr17Si25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce2Al47Fe\\n\",\n        \"output\": \" No, Ce2Al47Fe does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf3Ni7\\n\",\n        \"output\": \" Yes, Hf3Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Ti4Si11\\n\",\n        \"output\": \" Yes, Zr5Ti4Si11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd2MgNi2\\n\",\n        \"output\": \" Yes, Nd2MgNi2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe17NiB2\\n\",\n        \"output\": \" Yes, Fe17NiB2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf83Nb2Si15\\n\",\n        \"output\": \" Yes, Hf83Nb2Si15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La43Al3Ni4\\n\",\n        \"output\": \" Yes, La43Al3Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La(Al6Ni)7\\n\",\n        \"output\": \" Yes, La(Al6Ni)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al7CrSi2\\n\",\n        \"output\": \" No, Al7CrSi2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAlCu23\\n\",\n        \"output\": \" No, CeAlCu23 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe67.5Si10B22.5\\n\",\n        \"output\": \" Yes, Fe67.5Si10B22.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Al\\n\",\n        \"output\": \" No, Zr3Al does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" CrFe3B\\n\",\n        \"output\": \" Yes, CrFe3B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr11(TiSi2)3\\n\",\n        \"output\": \" Yes, Zr11(TiSi2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe16B4Mo5\\n\",\n        \"output\": \" Yes, Fe16B4Mo5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si3Ni33B14\\n\",\n        \"output\": \" Yes, Si3Ni33B14 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr51V20Ni29\\n\",\n        \"output\": \" Yes, Zr51V20Ni29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co70.5Si14.75B14.75\\n\",\n        \"output\": \" Yes, Co70.5Si14.75B14.75 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl8V\\n\",\n        \"output\": \" No, CeAl8V does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr29V10Ni11\\n\",\n        \"output\": \" Yes, Zr29V10Ni11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7(Fe26B5)3\\n\",\n        \"output\": \" Yes, Zr7(Fe26B5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe81B17F2\\n\",\n        \"output\": \" Yes, Fe81B17F2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al10Co29B11\\n\",\n        \"output\": \" No, Al10Co29B11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Cu5Ni2\\n\",\n        \"output\": \" Yes, Ti3Cu5Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb15Si4Mo\\n\",\n        \"output\": \" Yes, Nb15Si4Mo has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Al11Si6\\n\",\n        \"output\": \" Yes, Mn3Al11Si6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiCu\\n\",\n        \"output\": \" Yes, TiCu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca7Mg3\\n\",\n        \"output\": \" Yes, Ca7Mg3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr57.6Al10Ni32.4\\n\",\n        \"output\": \" Yes, Zr57.6Al10Ni32.4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf21Nb22Cu57\\n\",\n        \"output\": \" Yes, Hf21Nb22Cu57 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Ti5Cu12\\n\",\n        \"output\": \" Yes, Zr3Ti5Cu12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Fe90B7\\n\",\n        \"output\": \" No, Zr3Fe90B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti3Si17\\n\",\n        \"output\": \" Yes, Ti3Si17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y(Mg2Cu)3\\n\",\n        \"output\": \" Yes, Y(Mg2Cu)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Al93Cr5\\n\",\n        \"output\": \" No, Ce2Al93Cr5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr40Ni59Pd\\n\",\n        \"output\": \" Yes, Zr40Ni59Pd has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe36Ni5B9\\n\",\n        \"output\": \" Yes, Fe36Ni5B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf53V32Si15\\n\",\n        \"output\": \" Yes, Hf53V32Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5(Fe4B)9\\n\",\n        \"output\": \" Yes, Cr5(Fe4B)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti14Si4Ni7\\n\",\n        \"output\": \" Yes, Ti14Si4Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe19.5Ni58.5B22\\n\",\n        \"output\": \" Yes, Fe19.5Ni58.5B22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si4(Ni6B)3\\n\",\n        \"output\": \" Yes, Si4(Ni6B)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe37SiB12\\n\",\n        \"output\": \" No, Fe37SiB12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Al41Ni6\\n\",\n        \"output\": \" No, Mn3Al41Ni6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr35Al13Ni2\\n\",\n        \"output\": \" Yes, Zr35Al13Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu81.9Ag10.5P7.6\\n\",\n        \"output\": \" Yes, Cu81.9Ag10.5P7.6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La5Mg2Ni3\\n\",\n        \"output\": \" No, La5Mg2Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" millisecond\\n\",\n        \"output\": \" millisecond is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd5Al43Ni2\\n\",\n        \"output\": \" Yes, Nd5Al43Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7Al6Ni7\\n\",\n        \"output\": \" Yes, Zr7Al6Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5P16C6.5\\n\",\n        \"output\": \" Yes, Fe77.5P16C6.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe20B3P2\\n\",\n        \"output\": \" Yes, Fe20B3P2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr13Ti4Si3\\n\",\n        \"output\": \" Yes, Zr13Ti4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe33Cu10B7\\n\",\n        \"output\": \" No, Fe33Cu10B7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al4Co35B11\\n\",\n        \"output\": \" Yes, Al4Co35B11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce2Al3Cu20\\n\",\n        \"output\": \" Yes, Ce2Al3Cu20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr45(Al3Ni2)11\\n\",\n        \"output\": \" Yes, Zr45(Al3Ni2)11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe77.5Si13.5B9\\n\",\n        \"output\": \" Yes, Fe77.5Si13.5B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al89Co5Ni6\\n\",\n        \"output\": \" No, Al89Co5Ni6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al23FeCo\\n\",\n        \"output\": \" No, Al23FeCo does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" roll\\n\",\n        \"output\": \" roll is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe63Cu20Ag17\\n\",\n        \"output\": \" No, Fe63Cu20Ag17 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn63Co21B16\\n\",\n        \"output\": \" Yes, Mn63Co21B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr2.5La60.5Cu37\\n\",\n        \"output\": \" Yes, Sr2.5La60.5Cu37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca7.5Al92.5\\n\",\n        \"output\": \" No, Ca7.5Al92.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ghana\\n\",\n        \"output\": \" ghana is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr11.4Cr11.6Co77\\n\",\n        \"output\": \" Yes, Zr11.4Cr11.6Co77 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" toe\\n\",\n        \"output\": \" toe is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd2Mg11Ni7\\n\",\n        \"output\": \" Yes, Nd2Mg11Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La(Mg2Ni)3\\n\",\n        \"output\": \" Yes, La(Mg2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al16Fe\\n\",\n        \"output\": \" No, Ce3Al16Fe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg13Ni6\\n\",\n        \"output\": \" Yes, NdMg13Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeMn2Al47\\n\",\n        \"output\": \" No, CeMn2Al47 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15Si3Mo2\\n\",\n        \"output\": \" Yes, Zr15Si3Mo2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al8(Fe5B)7\\n\",\n        \"output\": \" Yes, Al8(Fe5B)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MgAl2Pd\\n\",\n        \"output\": \" No, MgAl2Pd does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La9Al15Ni26\\n\",\n        \"output\": \" Yes, La9Al15Ni26 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si5BMo14\\n\",\n        \"output\": \" No, Si5BMo14 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Y3Mg5Ni2\\n\",\n        \"output\": \" Yes, Y3Mg5Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ta2Ni3\\n\",\n        \"output\": \" Yes, Ta2Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf78V7Si15\\n\",\n        \"output\": \" Yes, Hf78V7Si15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe43W4C3\\n\",\n        \"output\": \" No, Fe43W4C3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al4Fe35B11\\n\",\n        \"output\": \" Yes, Al4Fe35B11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti3Al2Cu5\\n\",\n        \"output\": \" Yes, Ti3Al2Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ta5CoNi4\\n\",\n        \"output\": \" Yes, Ta5CoNi4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al85CoNi14\\n\",\n        \"output\": \" No, Al85CoNi14 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti5FeCu4\\n\",\n        \"output\": \" Yes, Ti5FeCu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La73Cu27\\n\",\n        \"output\": \" Yes, La73Cu27 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5Co79Mo16\\n\",\n        \"output\": \" Yes, Zr5Co79Mo16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb3Co17\\n\",\n        \"output\": \" Yes, Nb3Co17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu11Si19.5Pd69.5\\n\",\n        \"output\": \" Yes, Cu11Si19.5Pd69.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr5Co11B4\\n\",\n        \"output\": \" Yes, Cr5Co11B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu14.5Si16.5Pd69\\n\",\n        \"output\": \" Yes, Cu14.5Si16.5Pd69 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La3Zr5Fe42\\n\",\n        \"output\": \" Yes, La3Zr5Fe42 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr16Fe25C9\\n\",\n        \"output\": \" Yes, Cr16Fe25C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10(Fe7Ni3)9\\n\",\n        \"output\": \" Yes, Zr10(Fe7Ni3)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe8GeB\\n\",\n        \"output\": \" Yes, Fe8GeB has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Cu13\\n\",\n        \"output\": \" Yes, Zr7Cu13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si16.5Ni19.2Pd64.3\\n\",\n        \"output\": \" Yes, Si16.5Ni19.2Pd64.3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti7Ni13\\n\",\n        \"output\": \" No, Ti7Ni13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co2Ni81P17\\n\",\n        \"output\": \" No, Co2Ni81P17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr9V8Si3\\n\",\n        \"output\": \" Yes, Zr9V8Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80Si2.5P17.5\\n\",\n        \"output\": \" Yes, Fe80Si2.5P17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co18B7\\n\",\n        \"output\": \" Yes, Co18B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm5Al87Ni8\\n\",\n        \"output\": \" Yes, Sm5Al87Ni8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Al29Ni16\\n\",\n        \"output\": \" Yes, Zr5Al29Ni16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe37Ni10B3\\n\",\n        \"output\": \" No, Fe37Ni10B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr24Fe55B21\\n\",\n        \"output\": \" Yes, Cr24Fe55B21 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe77.5Si12.5B10\\n\",\n        \"output\": \" Yes, Fe77.5Si12.5B10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr5(Fe3Co2)9\\n\",\n        \"output\": \" Yes, Zr5(Fe3Co2)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti4SiNi5\\n\",\n        \"output\": \" Yes, Ti4SiNi5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl7Fe2\\n\",\n        \"output\": \" No, CeAl7Fe2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" reward\\n\",\n        \"output\": \" reward is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd15Fe77.5B7.5\\n\",\n        \"output\": \" Yes, Nd15Fe77.5B7.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4(Fe25B7)3\\n\",\n        \"output\": \" Yes, Zr4(Fe25B7)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe38Ni5B7\\n\",\n        \"output\": \" Yes, Fe38Ni5B7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2Co17B\\n\",\n        \"output\": \" Yes, Zr2Co17B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr22Ni17Mo61\\n\",\n        \"output\": \" No, Cr22Ni17Mo61 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr51.2Al20Ni28.8\\n\",\n        \"output\": \" Yes, Zr51.2Al20Ni28.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe19Ni19B12\\n\",\n        \"output\": \" Yes, Fe19Ni19B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe12.3Ni64.7B23\\n\",\n        \"output\": \" Yes, Fe12.3Ni64.7B23 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si21Pd79\\n\",\n        \"output\": \" Yes, Si21Pd79 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce11Al5Ni4\\n\",\n        \"output\": \" Yes, Ce11Al5Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr56.95Fe15Ni28.05\\n\",\n        \"output\": \" Yes, Zr56.95Fe15Ni28.05 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co34Mo5C11\\n\",\n        \"output\": \" Yes, Co34Mo5C11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr15Cu4B\\n\",\n        \"output\": \" Yes, Zr15Cu4B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La2Al17Cu\\n\",\n        \"output\": \" Yes, La2Al17Cu has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" HfCu3Ni\\n\",\n        \"output\": \" Yes, HfCu3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr28Ti41Cu31\\n\",\n        \"output\": \" No, Zr28Ti41Cu31 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Al14Ni3\\n\",\n        \"output\": \" Yes, Ce3Al14Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si18Pd79Au3\\n\",\n        \"output\": \" Yes, Si18Pd79Au3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13Ta4Ge3\\n\",\n        \"output\": \" Yes, Zr13Ta4Ge3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81B9P10\\n\",\n        \"output\": \" Yes, Fe81B9P10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La11Al4Cu5\\n\",\n        \"output\": \" Yes, La11Al4Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr10Al0.09Fe89.91\\n\",\n        \"output\": \" Yes, Zr10Al0.09Fe89.91 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr29Cu70B\\n\",\n        \"output\": \" Yes, Zr29Cu70B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co23Mo16C11\\n\",\n        \"output\": \" Yes, Co23Mo16C11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr8(VCo13)3\\n\",\n        \"output\": \" Yes, Zr8(VCo13)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce3NbAl16\\n\",\n        \"output\": \" No, Ce3NbAl16 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Fe43B2\\n\",\n        \"output\": \" Yes, Zr5Fe43B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al88Fe5Ni7\\n\",\n        \"output\": \" No, Al88Fe5Ni7 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu80.5Ag10.5P9\\n\",\n        \"output\": \" No, Cu80.5Ag10.5P9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11Al4Cu5\\n\",\n        \"output\": \" Yes, Zr11Al4Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Pr67.5B10Au22.5\\n\",\n        \"output\": \" Yes, Pr67.5B10Au22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr14.8V16Co69.2\\n\",\n        \"output\": \" Yes, Zr14.8V16Co69.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Hf7CuNi2\\n\",\n        \"output\": \" Yes, Hf7CuNi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Al4Ni3\\n\",\n        \"output\": \" No, Zr3Al4Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7AlCu2\\n\",\n        \"output\": \" No, La7AlCu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al15Ni3Mo2\\n\",\n        \"output\": \" Yes, Al15Ni3Mo2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe41(SiB2)3\\n\",\n        \"output\": \" Yes, Fe41(SiB2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr57Nb30Si13\\n\",\n        \"output\": \" Yes, Zr57Nb30Si13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdFe\\n\",\n        \"output\": \" Yes, NdFe has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr13Nb4Si3\\n\",\n        \"output\": \" Yes, Zr13Nb4Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" maple\\n\",\n        \"output\": \" maple is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce4AlCu45\\n\",\n        \"output\": \" No, Ce4AlCu45 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La7Mg10Ni3\\n\",\n        \"output\": \" Yes, La7Mg10Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe80Si2.5B17.5\\n\",\n        \"output\": \" Yes, Fe80Si2.5B17.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe73Si9.5B17.5\\n\",\n        \"output\": \" Yes, Fe73Si9.5B17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al16VCu3\\n\",\n        \"output\": \" Yes, Al16VCu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Co20B3C2\\n\",\n        \"output\": \" No, Co20B3C2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6Cu3Ni\\n\",\n        \"output\": \" Yes, Zr6Cu3Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe77Cu5B18\\n\",\n        \"output\": \" No, Fe77Cu5B18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg9\\n\",\n        \"output\": \" No, NdMg9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr27Ni15Mo8\\n\",\n        \"output\": \" Yes, Cr27Ni15Mo8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe36Cu23Ag41\\n\",\n        \"output\": \" Yes, Fe36Cu23Ag41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce6Cu39Ag55\\n\",\n        \"output\": \" Yes, Ce6Cu39Ag55 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn5Al8Si7\\n\",\n        \"output\": \" No, Mn5Al8Si7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti5Al2Ni3\\n\",\n        \"output\": \" Yes, Ti5Al2Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni18Mo4C3\\n\",\n        \"output\": \" No, Ni18Mo4C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co80Si7.5B12.5\\n\",\n        \"output\": \" Yes, Co80Si7.5B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg7Cu2\\n\",\n        \"output\": \" Yes, NdMg7Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79B8P13\\n\",\n        \"output\": \" Yes, Fe79B8P13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si3B5Mo12\\n\",\n        \"output\": \" No, Si3B5Mo12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" destruction\\n\",\n        \"output\": \" destruction is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr40FeCu59\\n\",\n        \"output\": \" Yes, Zr40FeCu59 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr7Al3\\n\",\n        \"output\": \" No, Zr7Al3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr12Fe83B5\\n\",\n        \"output\": \" Yes, Zr12Fe83B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu13Ag12\\n\",\n        \"output\": \" No, Cu13Ag12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" mailman\\n\",\n        \"output\": \" mailman is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr13Fe85B2\\n\",\n        \"output\": \" Yes, Zr13Fe85B2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si5(Ni11B4)3\\n\",\n        \"output\": \" Yes, Si5(Ni11B4)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co9Ni69.5P21.5\\n\",\n        \"output\": \" No, Co9Ni69.5P21.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" P19Ir40Pd41\\n\",\n        \"output\": \" Yes, P19Ir40Pd41 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr10Al22.5Fe67.5\\n\",\n        \"output\": \" Yes, Zr10Al22.5Fe67.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn29.5Co46.5B24\\n\",\n        \"output\": \" Yes, Mn29.5Co46.5B24 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" great-grandmother\\n\",\n        \"output\": \" great-grandmother is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al48FeCo\\n\",\n        \"output\": \" No, Al48FeCo does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" slash\\n\",\n        \"output\": \" slash is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca4La67Cu29\\n\",\n        \"output\": \" Yes, Ca4La67Cu29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce3Al16Co\\n\",\n        \"output\": \" No, Ce3Al16Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" grape\\n\",\n        \"output\": \" grape is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn(Al11Co)2\\n\",\n        \"output\": \" No, Mn(Al11Co)2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9Co11\\n\",\n        \"output\": \" Yes, Zr9Co11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti11Si2Ni7\\n\",\n        \"output\": \" Yes, Ti11Si2Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La11(Al2Ni)3\\n\",\n        \"output\": \" Yes, La11(Al2Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni16BP3\\n\",\n        \"output\": \" Yes, Ni16BP3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr40Fe47C13\\n\",\n        \"output\": \" No, Cr40Fe47C13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe41(BMo2)3\\n\",\n        \"output\": \" No, Fe41(BMo2)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd7(Al29Ni2)3\\n\",\n        \"output\": \" Yes, Nd7(Al29Ni2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce10(Al29Cr)3\\n\",\n        \"output\": \" Yes, Ce10(Al29Cr)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeCu8Ag11\\n\",\n        \"output\": \" Yes, CeCu8Ag11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAl13Ni6\\n\",\n        \"output\": \" Yes, CeAl13Ni6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce10Al83Cr7\\n\",\n        \"output\": \" No, Ce10Al83Cr7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr9Co7B4\\n\",\n        \"output\": \" Yes, Cr9Co7B4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe81Si4B15\\n\",\n        \"output\": \" Yes, Fe81Si4B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl16Ni3\\n\",\n        \"output\": \" Yes, CeAl16Ni3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" La10Al7Cu3\\n\",\n        \"output\": \" Yes, La10Al7Cu3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr23Ti5Cu22\\n\",\n        \"output\": \" Yes, Zr23Ti5Cu22 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Fe73B22\\n\",\n        \"output\": \" Yes, Zr5Fe73B22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" kilogram\\n\",\n        \"output\": \" kilogram is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7Fe79.9B13.1\\n\",\n        \"output\": \" Yes, Nb7Fe79.9B13.1 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si8Ni75B17\\n\",\n        \"output\": \" Yes, Si8Ni75B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr14(Fe3C)9\\n\",\n        \"output\": \" Yes, Cr14(Fe3C)9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ce4Cu43Ag3\\n\",\n        \"output\": \" No, Ce4Cu43Ag3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce4Al7Cu39\\n\",\n        \"output\": \" No, Ce4Al7Cu39 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co65W17.5C17.5\\n\",\n        \"output\": \" No, Co65W17.5C17.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Al87.5Ni7.5\\n\",\n        \"output\": \" No, Zr5Al87.5Ni7.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti11SiNi8\\n\",\n        \"output\": \" Yes, Ti11SiNi8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni29Mo16C5\\n\",\n        \"output\": \" No, Ni29Mo16C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti19Al31\\n\",\n        \"output\": \" Yes, Ti19Al31 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Cu77Ag20\\n\",\n        \"output\": \" No, Ce3Cu77Ag20 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La9Al10Ni\\n\",\n        \"output\": \" Yes, La9Al10Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al\\n\",\n        \"output\": \" No, Al does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr10Ti7Si3\\n\",\n        \"output\": \" Yes, Zr10Ti7Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg45Al4Ga\\n\",\n        \"output\": \" No, Mg45Al4Ga does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" mice\\n\",\n        \"output\": \" mice is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn21.6Co46.4B32\\n\",\n        \"output\": \" Yes, Mn21.6Co46.4B32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y11Al89\\n\",\n        \"output\": \" Yes, Y11Al89 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce3Al6Cu41\\n\",\n        \"output\": \" No, Ce3Al6Cu41 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd5(Mg3Ni2)3\\n\",\n        \"output\": \" Yes, Nd5(Mg3Ni2)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe29Cu8Ag63\\n\",\n        \"output\": \" No, Fe29Cu8Ag63 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si12.5B20Mo67.5\\n\",\n        \"output\": \" Yes, Si12.5B20Mo67.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3MgAg\\n\",\n        \"output\": \" No, Y3MgAg does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAl23Co\\n\",\n        \"output\": \" No, MnAl23Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr4Fe41B5\\n\",\n        \"output\": \" No, Cr4Fe41B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al59Cr19Si22\\n\",\n        \"output\": \" No, Al59Cr19Si22 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti31Ni15B4\\n\",\n        \"output\": \" Yes, Ti31Ni15B4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si2.5B20Mo77.5\\n\",\n        \"output\": \" No, Si2.5B20Mo77.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr17.5Cr6Co76.5\\n\",\n        \"output\": \" Yes, Zr17.5Cr6Co76.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al46Co3Ni\\n\",\n        \"output\": \" No, Al46Co3Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" LaMg5Cu4\\n\",\n        \"output\": \" Yes, LaMg5Cu4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" mouth\\n\",\n        \"output\": \" mouth is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe79(B4P3)3\\n\",\n        \"output\": \" Yes, Fe79(B4P3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" MnAl48Ni\\n\",\n        \"output\": \" No, MnAl48Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si8(Pd13Au)3\\n\",\n        \"output\": \" Yes, Si8(Pd13Au)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe16Si3B\\n\",\n        \"output\": \" Yes, Fe16Si3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Mg2Ag5\\n\",\n        \"output\": \" No, Y3Mg2Ag5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe7Ni76B17\\n\",\n        \"output\": \" Yes, Fe7Ni76B17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd8.4Co75.6Mo16\\n\",\n        \"output\": \" Yes, Gd8.4Co75.6Mo16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr16Si3Mo\\n\",\n        \"output\": \" Yes, Zr16Si3Mo has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La6AlCu3\\n\",\n        \"output\": \" Yes, La6AlCu3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn17.8Co71.2B11\\n\",\n        \"output\": \" Yes, Mn17.8Co71.2B11 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co20B2C3\\n\",\n        \"output\": \" No, Co20B2C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co20B4C\\n\",\n        \"output\": \" Yes, Co20B4C has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87Fe2Co11\\n\",\n        \"output\": \" Yes, Al87Fe2Co11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr11Fe35B4\\n\",\n        \"output\": \" No, Cr11Fe35B4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co78(SiB)11\\n\",\n        \"output\": \" Yes, Co78(SiB)11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ce2Cu23Ag25\\n\",\n        \"output\": \" Yes, Ce2Cu23Ag25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg18Cu\\n\",\n        \"output\": \" No, NdMg18Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La(AlNi)2\\n\",\n        \"output\": \" Yes, La(AlNi)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn6Co13B6\\n\",\n        \"output\": \" Yes, Mn6Co13B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn10(Co4B)3\\n\",\n        \"output\": \" Yes, Mn10(Co4B)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Y5Mg87Mn8\\n\",\n        \"output\": \" Yes, Y5Mg87Mn8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni17(P3Pd8)3\\n\",\n        \"output\": \" Yes, Ni17(P3Pd8)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg8AlZn\\n\",\n        \"output\": \" No, Mg8AlZn does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe77B19P4\\n\",\n        \"output\": \" No, Fe77B19P4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe72.5Si17.5B10\\n\",\n        \"output\": \" Yes, Fe72.5Si17.5B10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe21Co62B17\\n\",\n        \"output\": \" Yes, Fe21Co62B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y51Al15Cu34\\n\",\n        \"output\": \" Yes, Y51Al15Cu34 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr12.5Co80.5W7\\n\",\n        \"output\": \" Yes, Zr12.5Co80.5W7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti57Nb30Si13\\n\",\n        \"output\": \" No, Ti57Nb30Si13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si18Ni49.2Pd32.8\\n\",\n        \"output\": \" Yes, Si18Ni49.2Pd32.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al87CoNi12\\n\",\n        \"output\": \" Yes, Al87CoNi12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe59.5Ni20B20.5\\n\",\n        \"output\": \" Yes, Fe59.5Ni20B20.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La12Al3Ni5\\n\",\n        \"output\": \" Yes, La12Al3Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr27Fe62B11\\n\",\n        \"output\": \" Yes, Cr27Fe62B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr15Fe72B13\\n\",\n        \"output\": \" Yes, Zr15Fe72B13 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti10Si3Ni7\\n\",\n        \"output\": \" Yes, Ti10Si3Ni7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg4Ni\\n\",\n        \"output\": \" Yes, Mg4Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe85B11P4\\n\",\n        \"output\": \" No, Fe85B11P4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co85W2.5C12.5\\n\",\n        \"output\": \" No, Co85W2.5C12.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti7Al9Cu4\\n\",\n        \"output\": \" No, Ti7Al9Cu4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr6Fe39B5\\n\",\n        \"output\": \" Yes, Zr6Fe39B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al83Cr17\\n\",\n        \"output\": \" No, Al83Cr17 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn2Al20Ni3\\n\",\n        \"output\": \" No, Mn2Al20Ni3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr2Al43Ni5\\n\",\n        \"output\": \" Yes, Zr2Al43Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr13Be7\\n\",\n        \"output\": \" Yes, Zr13Be7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe82.5Si10B7.5\\n\",\n        \"output\": \" No, Fe82.5Si10B7.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn13.5Co54.5B32\\n\",\n        \"output\": \" Yes, Mn13.5Co54.5B32 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn5Ge18Pd77\\n\",\n        \"output\": \" Yes, Mn5Ge18Pd77 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Al3Cu5\\n\",\n        \"output\": \" Yes, Zr12Al3Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti15Si3Ni2\\n\",\n        \"output\": \" Yes, Ti15Si3Ni2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Fe41B6\\n\",\n        \"output\": \" Yes, Nd3Fe41B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" NiPd\\n\",\n        \"output\": \" Yes, NiPd has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti40Nb47Si13\\n\",\n        \"output\": \" No, Ti40Nb47Si13 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr15Nb2Ge3\\n\",\n        \"output\": \" Yes, Zr15Nb2Ge3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd4Al41Ni5\\n\",\n        \"output\": \" Yes, Nd4Al41Ni5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf34.2Zr41.8Fe24\\n\",\n        \"output\": \" Yes, Hf34.2Zr41.8Fe24 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrAl44Ni5\\n\",\n        \"output\": \" Yes, ZrAl44Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co82.5W10C7.5\\n\",\n        \"output\": \" No, Co82.5W10C7.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Al4Cu3\\n\",\n        \"output\": \" No, Ti3Al4Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe36Cu5B9\\n\",\n        \"output\": \" No, Fe36Cu5B9 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu(Ni25P8)3\\n\",\n        \"output\": \" No, Cu(Ni25P8)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe41Cu30Ag29\\n\",\n        \"output\": \" Yes, Fe41Cu30Ag29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta6Ti11Si3\\n\",\n        \"output\": \" Yes, Ta6Ti11Si3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cr5Fe77B18\\n\",\n        \"output\": \" Yes, Cr5Fe77B18 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni33Mo12C5\\n\",\n        \"output\": \" No, Ni33Mo12C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr9.4Co81.6Mo9\\n\",\n        \"output\": \" Yes, Zr9.4Co81.6Mo9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg3Al11Pd6\\n\",\n        \"output\": \" No, Mg3Al11Pd6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe13Si4C3\\n\",\n        \"output\": \" Yes, Fe13Si4C3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn17.5Co70.5B12\\n\",\n        \"output\": \" Yes, Mn17.5Co70.5B12 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe3B\\n\",\n        \"output\": \" Yes, Fe3B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe89Cu3B8\\n\",\n        \"output\": \" No, Fe89Cu3B8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr67Fe23.1Ni9.9\\n\",\n        \"output\": \" Yes, Zr67Fe23.1Ni9.9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe83.5Si6.5B10\\n\",\n        \"output\": \" No, Fe83.5Si6.5B10 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe45W2C3\\n\",\n        \"output\": \" No, Fe45W2C3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La43Al57\\n\",\n        \"output\": \" Yes, La43Al57 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeCu9Ag10\\n\",\n        \"output\": \" Yes, CeCu9Ag10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co17Mo3C5\\n\",\n        \"output\": \" Yes, Co17Mo3C5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr9Fe91\\n\",\n        \"output\": \" Yes, Zr9Fe91 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe41.5Co41.5B17\\n\",\n        \"output\": \" Yes, Fe41.5Co41.5B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mo12P5Rh8\\n\",\n        \"output\": \" Yes, Mo12P5Rh8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg4Ag3\\n\",\n        \"output\": \" Yes, Y3Mg4Ag3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Y3Mg12Ni5\\n\",\n        \"output\": \" Yes, Y3Mg12Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3AlCu\\n\",\n        \"output\": \" No, Ti3AlCu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd12Fe69.5B18.5\\n\",\n        \"output\": \" Yes, Nd12Fe69.5B18.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TaNb7Ni12\\n\",\n        \"output\": \" Yes, TaNb7Ni12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Er67.5B10Au22.5\\n\",\n        \"output\": \" Yes, Er67.5B10Au22.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiCu9\\n\",\n        \"output\": \" No, TiCu9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Sr7.5La64.5Cu28\\n\",\n        \"output\": \" Yes, Sr7.5La64.5Cu28 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni41(B2C)3\\n\",\n        \"output\": \" No, Ni41(B2C)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Fe40B7\\n\",\n        \"output\": \" Yes, Zr3Fe40B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si12.5Ni75B12.5\\n\",\n        \"output\": \" Yes, Si12.5Ni75B12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe16Cu5B4\\n\",\n        \"output\": \" No, Fe16Cu5B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" ZrTi16Si3\\n\",\n        \"output\": \" Yes, ZrTi16Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr3AlNi\\n\",\n        \"output\": \" Yes, Zr3AlNi has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3.8Ni78B18.2\\n\",\n        \"output\": \" Yes, Ti3.8Ni78B18.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe9Ag11\\n\",\n        \"output\": \" No, Fe9Ag11 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe17Ni5B3\\n\",\n        \"output\": \" Yes, Fe17Ni5B3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" turtle\\n\",\n        \"output\": \" turtle is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti10FeCu9\\n\",\n        \"output\": \" Yes, Ti10FeCu9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe2Co2B\\n\",\n        \"output\": \" Yes, Fe2Co2B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CeAl15Cu4\\n\",\n        \"output\": \" No, CeAl15Cu4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni27Mo14C9\\n\",\n        \"output\": \" No, Ni27Mo14C9 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb7(Fe28B3)3\\n\",\n        \"output\": \" Yes, Nb7(Fe28B3)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr7Fe37B6\\n\",\n        \"output\": \" Yes, Cr7Fe37B6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce3Al16Cr\\n\",\n        \"output\": \" No, Ce3Al16Cr does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr76(Ti3Si5)3\\n\",\n        \"output\": \" Yes, Zr76(Ti3Si5)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ce8Al89Cr3\\n\",\n        \"output\": \" No, Ce8Al89Cr3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Mg12Cu5\\n\",\n        \"output\": \" Yes, Y3Mg12Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al45Fe4Co\\n\",\n        \"output\": \" No, Al45Fe4Co does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg7(Ti2Al)6\\n\",\n        \"output\": \" No, Mg7(Ti2Al)6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr83Si17\\n\",\n        \"output\": \" Yes, Zr83Si17 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe64B29N7\\n\",\n        \"output\": \" Yes, Fe64B29N7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr2(CrCo5)3\\n\",\n        \"output\": \" Yes, Zr2(CrCo5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si5Ni14C\\n\",\n        \"output\": \" No, Si5Ni14C does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al44Co5Ni\\n\",\n        \"output\": \" No, Al44Co5Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr15Ni9B\\n\",\n        \"output\": \" Yes, Zr15Ni9B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg4(AlZn)3\\n\",\n        \"output\": \" No, Mg4(AlZn)3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe39W6C5\\n\",\n        \"output\": \" No, Fe39W6C5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe91Ni5B4\\n\",\n        \"output\": \" No, Fe91Ni5B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe73B20Mo7\\n\",\n        \"output\": \" Yes, Fe73B20Mo7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb6.8Fe76B17.2\\n\",\n        \"output\": \" Yes, Nb6.8Fe76B17.2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn19(Nb5Co22)3\\n\",\n        \"output\": \" Yes, Mn19(Nb5Co22)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Tb32.5Al2.5Fe65\\n\",\n        \"output\": \" Yes, Tb32.5Al2.5Fe65 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr8Co41B\\n\",\n        \"output\": \" Yes, Zr8Co41B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe7SiB2\\n\",\n        \"output\": \" Yes, Fe7SiB2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr32Ni43Mo25\\n\",\n        \"output\": \" Yes, Cr32Ni43Mo25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Si9Pd36Au5\\n\",\n        \"output\": \" Yes, Si9Pd36Au5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nd(MgNi)2\\n\",\n        \"output\": \" Yes, Nd(MgNi)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr(AlNi2)3\\n\",\n        \"output\": \" No, Zr(AlNi2)3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y3Al15Ni2\\n\",\n        \"output\": \" Yes, Y3Al15Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti12Al7Cu\\n\",\n        \"output\": \" No, Ti12Al7Cu does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" MnAl46Co3\\n\",\n        \"output\": \" No, MnAl46Co3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti42NbCu57\\n\",\n        \"output\": \" Yes, Ti42NbCu57 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CeAl17Fe2\\n\",\n        \"output\": \" Yes, CeAl17Fe2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe81.5Si4B14.5\\n\",\n        \"output\": \" Yes, Fe81.5Si4B14.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti17SiNi2\\n\",\n        \"output\": \" No, Ti17SiNi2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti9Al9Cu2\\n\",\n        \"output\": \" No, Ti9Al9Cu2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr60.3Co10Ni29.7\\n\",\n        \"output\": \" Yes, Zr60.3Co10Ni29.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al35Fe7Cu8\\n\",\n        \"output\": \" No, Al35Fe7Cu8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" shelf\\n\",\n        \"output\": \" shelf is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4Al33Ni13\\n\",\n        \"output\": \" Yes, Zr4Al33Ni13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39Cu5B6\\n\",\n        \"output\": \" No, Fe39Cu5B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni77P18W5\\n\",\n        \"output\": \" Yes, Ni77P18W5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ba2La11Cu7\\n\",\n        \"output\": \" Yes, Ba2La11Cu7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2Al89Ni9\\n\",\n        \"output\": \" Yes, Zr2Al89Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ba2La13Cu10\\n\",\n        \"output\": \" Yes, Ba2La13Cu10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr5Al79Ni16\\n\",\n        \"output\": \" Yes, Zr5Al79Ni16 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr53.6Mn20Ni26.4\\n\",\n        \"output\": \" Yes, Zr53.6Mn20Ni26.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co15(B4C)2\\n\",\n        \"output\": \" Yes, Co15(B4C)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si16.5Ni12.5Pd71\\n\",\n        \"output\": \" Yes, Si16.5Ni12.5Pd71 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf7Fe77B16\\n\",\n        \"output\": \" Yes, Hf7Fe77B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn15.5Al76Cu8.5\\n\",\n        \"output\": \" No, Mn15.5Al76Cu8.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co12.5Ni66P21.5\\n\",\n        \"output\": \" No, Co12.5Ni66P21.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr4(AlNi)3\\n\",\n        \"output\": \" Yes, Zr4(AlNi)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Pd76.5Au7\\n\",\n        \"output\": \" Yes, Si16.5Pd76.5Au7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" YMg59Cu40\\n\",\n        \"output\": \" Yes, YMg59Cu40 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr4.5Fe92B3.5\\n\",\n        \"output\": \" Yes, Zr4.5Fe92B3.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7.4Co86.2Mo6.4\\n\",\n        \"output\": \" Yes, Zr7.4Co86.2Mo6.4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe93NiB6\\n\",\n        \"output\": \" No, Fe93NiB6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni32B11C7\\n\",\n        \"output\": \" Yes, Ni32B11C7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe57Ni25B18\\n\",\n        \"output\": \" Yes, Fe57Ni25B18 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si11Pd39\\n\",\n        \"output\": \" Yes, Si11Pd39 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al36(FeNi)7\\n\",\n        \"output\": \" Yes, Al36(FeNi)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Tb1.3Fe79B19.7\\n\",\n        \"output\": \" Yes, Tb1.3Fe79B19.7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La4Mg11Cu5\\n\",\n        \"output\": \" Yes, La4Mg11Cu5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti16Si3Ni\\n\",\n        \"output\": \" Yes, Ti16Si3Ni has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al57Fe27Ni16\\n\",\n        \"output\": \" No, Al57Fe27Ni16 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe77P15C8\\n\",\n        \"output\": \" Yes, Fe77P15C8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cu2Ni18P5\\n\",\n        \"output\": \" Yes, Cu2Ni18P5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y2(Al5Ni)3\\n\",\n        \"output\": \" Yes, Y2(Al5Ni)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3VSi\\n\",\n        \"output\": \" No, Ti3VSi does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al13VCu6\\n\",\n        \"output\": \" Yes, Al13VCu6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" mom\\n\",\n        \"output\": \" mom is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" YAl15Ni4\\n\",\n        \"output\": \" No, YAl15Ni4 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La10Al7Ni3\\n\",\n        \"output\": \" Yes, La10Al7Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La5Al91Ni4\\n\",\n        \"output\": \" Yes, La5Al91Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sm1.3Fe79B19.7\\n\",\n        \"output\": \" Yes, Sm1.3Fe79B19.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ca15Mg3Cu2\\n\",\n        \"output\": \" Yes, Ca15Mg3Cu2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn2Co2B\\n\",\n        \"output\": \" Yes, Mn2Co2B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co17B3\\n\",\n        \"output\": \" No, Co17B3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" TiAl12Cu7\\n\",\n        \"output\": \" No, TiAl12Cu7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" GdAl18Ni\\n\",\n        \"output\": \" Yes, GdAl18Ni has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd(MgCu)2\\n\",\n        \"output\": \" Yes, Nd(MgCu)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg23(AlGa2)9\\n\",\n        \"output\": \" Yes, Mg23(AlGa2)9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al47Co2Ni\\n\",\n        \"output\": \" No, Al47Co2Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ghost\\n\",\n        \"output\": \" ghost is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al8Fe37B5\\n\",\n        \"output\": \" No, Al8Fe37B5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti3.36Fe80.64B16\\n\",\n        \"output\": \" Yes, Ti3.36Fe80.64B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe87NiB12\\n\",\n        \"output\": \" No, Fe87NiB12 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe81.5B18.5\\n\",\n        \"output\": \" Yes, Fe81.5B18.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al88Co11Ni\\n\",\n        \"output\": \" No, Al88Co11Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al11V4Ge5\\n\",\n        \"output\": \" No, Al11V4Ge5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn3Al45Ni2\\n\",\n        \"output\": \" No, Mn3Al45Ni2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ce2Mg7Cu\\n\",\n        \"output\": \" No, Ce2Mg7Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al69Fe13Cu18\\n\",\n        \"output\": \" No, Al69Fe13Cu18 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti32.3Nb25Cu42.7\\n\",\n        \"output\": \" Yes, Ti32.3Nb25Cu42.7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe39SiB10\\n\",\n        \"output\": \" Yes, Fe39SiB10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr37Ni63\\n\",\n        \"output\": \" Yes, Zr37Ni63 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" bail\\n\",\n        \"output\": \" bail is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe33Ni50B17\\n\",\n        \"output\": \" Yes, Fe33Ni50B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr5Co44Si\\n\",\n        \"output\": \" Yes, Zr5Co44Si has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni59Mo41\\n\",\n        \"output\": \" Yes, Ni59Mo41 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al89Fe3Ni8\\n\",\n        \"output\": \" No, Al89Fe3Ni8 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl15Ni4\\n\",\n        \"output\": \" Yes, LaAl15Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr13Al3Ni4\\n\",\n        \"output\": \" Yes, Zr13Al3Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al13Cr3Si4\\n\",\n        \"output\": \" No, Al13Cr3Si4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg6(CuAg)7\\n\",\n        \"output\": \" Yes, Mg6(CuAg)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr2Co2C\\n\",\n        \"output\": \" Yes, Cr2Co2C has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr14Al11Ni25\\n\",\n        \"output\": \" Yes, Zr14Al11Ni25 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" SiBMo8\\n\",\n        \"output\": \" No, SiBMo8 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn4Co16B5\\n\",\n        \"output\": \" Yes, Mn4Co16B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr13Cu6B\\n\",\n        \"output\": \" Yes, Zr13Cu6B has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu87Ag5.5P7.5\\n\",\n        \"output\": \" No, Cu87Ag5.5P7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb3Ni2\\n\",\n        \"output\": \" Yes, Nb3Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al11(CrSi2)3\\n\",\n        \"output\": \" Yes, Al11(CrSi2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe17B3Mo5\\n\",\n        \"output\": \" Yes, Fe17B3Mo5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Ti2Si5\\n\",\n        \"output\": \" Yes, Zr3Ti2Si5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Hf3Ni2\\n\",\n        \"output\": \" Yes, Hf3Ni2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf9Cu7Ni4\\n\",\n        \"output\": \" Yes, Hf9Cu7Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" CaAl8Ni\\n\",\n        \"output\": \" No, CaAl8Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn49(Co9B8)3\\n\",\n        \"output\": \" Yes, Mn49(Co9B8)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al79(FeNi2)7\\n\",\n        \"output\": \" Yes, Al79(FeNi2)7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr3Fe80B17\\n\",\n        \"output\": \" Yes, Zr3Fe80B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" football\\n\",\n        \"output\": \" football is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nd3Mg16Cu\\n\",\n        \"output\": \" No, Nd3Mg16Cu does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Al7Ni\\n\",\n        \"output\": \" No, Zr12Al7Ni does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Si16.5Ag10Pd73.5\\n\",\n        \"output\": \" Yes, Si16.5Ag10Pd73.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg10Ti53Al37\\n\",\n        \"output\": \" Yes, Mg10Ti53Al37 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2AlNi\\n\",\n        \"output\": \" Yes, Zr2AlNi has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al9Fe\\n\",\n        \"output\": \" No, Al9Fe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" airbus\\n\",\n        \"output\": \" airbus is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5(Fe9B)2\\n\",\n        \"output\": \" No, Cr5(Fe9B)2 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr3Al13Ni4\\n\",\n        \"output\": \" Yes, Zr3Al13Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe82Si5B13\\n\",\n        \"output\": \" Yes, Fe82Si5B13 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg4Zn\\n\",\n        \"output\": \" No, Mg4Zn does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nd3Al5Cu42\\n\",\n        \"output\": \" No, Nd3Al5Cu42 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" La2AlNi2\\n\",\n        \"output\": \" Yes, La2AlNi2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al13V4Cu3\\n\",\n        \"output\": \" No, Al13V4Cu3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co15B7C3\\n\",\n        \"output\": \" Yes, Co15B7C3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr12Fe33B5\\n\",\n        \"output\": \" Yes, Cr12Fe33B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr2Al16Ni7\\n\",\n        \"output\": \" Yes, Zr2Al16Ni7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe18B5Mo2\\n\",\n        \"output\": \" Yes, Fe18B5Mo2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y(CoB)2\\n\",\n        \"output\": \" Yes, Y(CoB)2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co95W2.5C2.5\\n\",\n        \"output\": \" No, Co95W2.5C2.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Hf54Zr3Be43\\n\",\n        \"output\": \" Yes, Hf54Zr3Be43 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe78Si15B7\\n\",\n        \"output\": \" Yes, Fe78Si15B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al71Si25Ni4\\n\",\n        \"output\": \" Yes, Al71Si25Ni4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr11La60Cu29\\n\",\n        \"output\": \" Yes, Sr11La60Cu29 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti7AlCu12\\n\",\n        \"output\": \" Yes, Ti7AlCu12 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb8.3Fe77.5B14.2\\n\",\n        \"output\": \" Yes, Nb8.3Fe77.5B14.2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nd3(Al10Ni)2\\n\",\n        \"output\": \" Yes, Nd3(Al10Ni)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cu3Ni38P9\\n\",\n        \"output\": \" Yes, Cu3Ni38P9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co77.5Si7.5B15\\n\",\n        \"output\": \" Yes, Co77.5Si7.5B15 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr6V5Ni9\\n\",\n        \"output\": \" Yes, Zr6V5Ni9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe40Cu31Ag29\\n\",\n        \"output\": \" No, Fe40Cu31Ag29 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr17Ge3\\n\",\n        \"output\": \" Yes, Zr17Ge3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Si2BW7\\n\",\n        \"output\": \" Yes, Si2BW7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co60Si17.5B22.5\\n\",\n        \"output\": \" No, Co60Si17.5B22.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" NdAl16Ni3\\n\",\n        \"output\": \" Yes, NdAl16Ni3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe29.5Ni50.5B20\\n\",\n        \"output\": \" Yes, Fe29.5Ni50.5B20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ba9La60Cu31\\n\",\n        \"output\": \" Yes, Ba9La60Cu31 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr49Cu50B\\n\",\n        \"output\": \" Yes, Zr49Cu50B has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe82(SiB5)3\\n\",\n        \"output\": \" Yes, Fe82(SiB5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr11.5Fe84B4.5\\n\",\n        \"output\": \" Yes, Zr11.5Fe84B4.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe83B12Mo5\\n\",\n        \"output\": \" Yes, Fe83B12Mo5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ti31Ni19\\n\",\n        \"output\": \" Yes, Ti31Ni19 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al46FeNi3\\n\",\n        \"output\": \" No, Al46FeNi3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" V5Fe38B7\\n\",\n        \"output\": \" Yes, V5Fe38B7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co12B8C5\\n\",\n        \"output\": \" No, Co12B8C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Al12CrSi7\\n\",\n        \"output\": \" No, Al12CrSi7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr5Fe89B6\\n\",\n        \"output\": \" No, Cr5Fe89B6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" TiCuNi3\\n\",\n        \"output\": \" No, TiCuNi3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" christopher\\n\",\n        \"output\": \" christopher is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3.5Al95.8Ni0.7\\n\",\n        \"output\": \" No, Ti3.5Al95.8Ni0.7 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ti3Al7Cu10\\n\",\n        \"output\": \" Yes, Ti3Al7Cu10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe21BP3\\n\",\n        \"output\": \" No, Fe21BP3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mg17Mn3\\n\",\n        \"output\": \" No, Mg17Mn3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Sr1.5La61.5Cu37\\n\",\n        \"output\": \" Yes, Sr1.5La61.5Cu37 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Gd7Al83Ni10\\n\",\n        \"output\": \" Yes, Gd7Al83Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni31Mo12C7\\n\",\n        \"output\": \" Yes, Ni31Mo12C7 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni26B19C5\\n\",\n        \"output\": \" Yes, Ni26B19C5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe61Ni20B19\\n\",\n        \"output\": \" Yes, Fe61Ni20B19 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg11Al2Ag7\\n\",\n        \"output\": \" Yes, Mg11Al2Ag7 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr12Ti3Si5\\n\",\n        \"output\": \" Yes, Zr12Ti3Si5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Si16.5Ag6Pd77.5\\n\",\n        \"output\": \" Yes, Si16.5Ag6Pd77.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Nb9.1Fe79.9B11\\n\",\n        \"output\": \" Yes, Nb9.1Fe79.9B11 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn4Al41Ni5\\n\",\n        \"output\": \" No, Mn4Al41Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Ni81.5B16.7P1.8\\n\",\n        \"output\": \" Yes, Ni81.5B16.7P1.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" chard\\n\",\n        \"output\": \" chard is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co14Ni67P19\\n\",\n        \"output\": \" No, Co14Ni67P19 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr63Al27Ni10\\n\",\n        \"output\": \" Yes, Zr63Al27Ni10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Cu78.5Ag14P7.5\\n\",\n        \"output\": \" No, Cu78.5Ag14P7.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y7.5Mg90.5Mn2\\n\",\n        \"output\": \" No, Y7.5Mg90.5Mn2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ca6Al3Ga\\n\",\n        \"output\": \" Yes, Ca6Al3Ga has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni41B5C4\\n\",\n        \"output\": \" No, Ni41B5C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe82.5P15C2.5\\n\",\n        \"output\": \" Yes, Fe82.5P15C2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Al24Fe\\n\",\n        \"output\": \" No, Al24Fe does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni16B7C2\\n\",\n        \"output\": \" Yes, Ni16B7C2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Fe37Ni5B8\\n\",\n        \"output\": \" Yes, Fe37Ni5B8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" CrFe7B2\\n\",\n        \"output\": \" Yes, CrFe7B2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr2(CrFe5)3\\n\",\n        \"output\": \" Yes, Zr2(CrFe5)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe33Mo8C9\\n\",\n        \"output\": \" Yes, Fe33Mo8C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" NdMg3Cu\\n\",\n        \"output\": \" Yes, NdMg3Cu has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mg13AlZn6\\n\",\n        \"output\": \" Yes, Mg13AlZn6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Hf12.2Fe51.5O36.3\\n\",\n        \"output\": \" No, Hf12.2Fe51.5O36.3 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni63P20Pd17\\n\",\n        \"output\": \" Yes, Ni63P20Pd17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Nb20Si4Ge\\n\",\n        \"output\": \" Yes, Nb20Si4Ge has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" CeAl17Co2\\n\",\n        \"output\": \" Yes, CeAl17Co2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb12Fe85B3\\n\",\n        \"output\": \" No, Nb12Fe85B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr13Fe28C9\\n\",\n        \"output\": \" Yes, Cr13Fe28C9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mg17AlZn2\\n\",\n        \"output\": \" No, Mg17AlZn2 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al69V6Ge25\\n\",\n        \"output\": \" Yes, Al69V6Ge25 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Mn20Al53Si27\\n\",\n        \"output\": \" Yes, Mn20Al53Si27 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Co67.5W20C12.5\\n\",\n        \"output\": \" No, Co67.5W20C12.5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti15Nb2Si3\\n\",\n        \"output\": \" Yes, Ti15Nb2Si3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ca7.5Mg82.5Cu10\\n\",\n        \"output\": \" Yes, Ca7.5Mg82.5Cu10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr19Co22C9\\n\",\n        \"output\": \" Yes, Cr19Co22C9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe39Si2B9\\n\",\n        \"output\": \" Yes, Fe39Si2B9 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr6.5Cr8Co85.5\\n\",\n        \"output\": \" Yes, Zr6.5Cr8Co85.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co12B9C4\\n\",\n        \"output\": \" No, Co12B9C4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Nb5Ni78B17\\n\",\n        \"output\": \" Yes, Nb5Ni78B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Cr5Fe91B4\\n\",\n        \"output\": \" No, Cr5Fe91B4 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Mn6Co14B5\\n\",\n        \"output\": \" Yes, Mn6Co14B5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr7(Al2Ni7)2\\n\",\n        \"output\": \" Yes, Zr7(Al2Ni7)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cr10Fe37B3\\n\",\n        \"output\": \" No, Cr10Fe37B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" shrimp\\n\",\n        \"output\": \" shrimp is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Al11Cr4Si5\\n\",\n        \"output\": \" No, Al11Cr4Si5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co14Ni64.5P21.5\\n\",\n        \"output\": \" No, Co14Ni64.5P21.5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Fe75P12.5C12.5\\n\",\n        \"output\": \" Yes, Fe75P12.5C12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe77B13P10\\n\",\n        \"output\": \" Yes, Fe77B13P10 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Cr2Fe7B\\n\",\n        \"output\": \" No, Cr2Fe7B does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr7.5V20Co72.5\\n\",\n        \"output\": \" Yes, Zr7.5V20Co72.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Fe1.7Si16.5Pd81.8\\n\",\n        \"output\": \" Yes, Fe1.7Si16.5Pd81.8 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Zr42.5Cu50B7.5\\n\",\n        \"output\": \" Yes, Zr42.5Cu50B7.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Y11Al5Ni4\\n\",\n        \"output\": \" Yes, Y11Al5Ni4 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" La3Al2Ni5\\n\",\n        \"output\": \" Yes, La3Al2Ni5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ti52.5Nb30Si17.5\\n\",\n        \"output\": \" Yes, Ti52.5Nb30Si17.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Sr8La25Cu17\\n\",\n        \"output\": \" Yes, Sr8La25Cu17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Mn15Fe79B6\\n\",\n        \"output\": \" No, Mn15Fe79B6 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ta2(Ti5Si)3\\n\",\n        \"output\": \" Yes, Ta2(Ti5Si)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ni14P5Pd6\\n\",\n        \"output\": \" Yes, Ni14P5Pd6 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al6Fe41B3\\n\",\n        \"output\": \" No, Al6Fe41B3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr71Ti9Si20\\n\",\n        \"output\": \" Yes, Zr71Ti9Si20 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3Ti3Be4\\n\",\n        \"output\": \" Yes, Zr3Ti3Be4 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe71Si7B22\\n\",\n        \"output\": \" Yes, Fe71Si7B22 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co72.5W15C12.5\\n\",\n        \"output\": \" Yes, Co72.5W15C12.5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" La6Mg9Cu5\\n\",\n        \"output\": \" Yes, La6Mg9Cu5 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu81.5Ag10.5P8\\n\",\n        \"output\": \" Yes, Cu81.5Ag10.5P8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn2Co18B5\\n\",\n        \"output\": \" Yes, Mn2Co18B5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr77.5Cu20B2.5\\n\",\n        \"output\": \" Yes, Zr77.5Cu20B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Tb32.5Fe65Si2.5\\n\",\n        \"output\": \" Yes, Tb32.5Fe65Si2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr3(Fe10B)2\\n\",\n        \"output\": \" Yes, Zr3(Fe10B)2 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Cu6.7Si16.5Pd76.8\\n\",\n        \"output\": \" Yes, Cu6.7Si16.5Pd76.8 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" LaAl18Ni\\n\",\n        \"output\": \" No, LaAl18Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Zr4(CuNi)3\\n\",\n        \"output\": \" Yes, Zr4(CuNi)3 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al89Co6Ni5\\n\",\n        \"output\": \" No, Al89Co6Ni5 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ti3CuNi6\\n\",\n        \"output\": \" No, Ti3CuNi6 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Zr7(Fe29B2)3\\n\",\n        \"output\": \" Yes, Zr7(Fe29B2)3 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" ZrAl8Ni\\n\",\n        \"output\": \" No, ZrAl8Ni does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" LaAl39Ni10\\n\",\n        \"output\": \" Yes, LaAl39Ni10 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Co13B7C5\\n\",\n        \"output\": \" No, Co13B7C5 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" V5Fe79B16\\n\",\n        \"output\": \" Yes, V5Fe79B16 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr18SiNi6\\n\",\n        \"output\": \" Yes, Zr18SiNi6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" Ni37B13\\n\",\n        \"output\": \" No, Ni37B13 does not have glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe83Si2B15\\n\",\n        \"output\": \" Yes, Fe83Si2B15 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al4Co37B9\\n\",\n        \"output\": \" Yes, Al4Co37B9 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" bill\\n\",\n        \"output\": \" bill is not a composition and it has no relation with glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Mn27Co17B6\\n\",\n        \"output\": \" Yes, Mn27Co17B6 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Co18B5C2\\n\",\n        \"output\": \" Yes, Co18B5C2 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass-forming ability? ->\",\n        \"input\": \" vessel\\n\",\n        \"output\": \" vessel is not a composition and it has no relation with glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Fe39Ag61\\n\",\n        \"output\": \" No, Fe39Ag61 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Nb7Si2W\\n\",\n        \"output\": \" Yes, Nb7Si2W has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Al45Co2Ni3\\n\",\n        \"output\": \" No, Al45Co2Ni3 does not have glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass-forming ability. ->\",\n        \"input\": \" Ta10Ni73B17\\n\",\n        \"output\": \" Yes, Ta10Ni73B17 has glass-forming ability.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me if given composition has glass formation ability. ->\",\n        \"input\": \" Zr72.5Cu25B2.5\\n\",\n        \"output\": \" Yes, Zr72.5Cu25B2.5 has glass formation ability.\\n\"\n    },\n    {\n        \"instruction\": \"Does given composition have glass formation ability? ->\",\n        \"input\": \" Ni73(B5C4)3\\n\",\n        \"output\": \" No, Ni73(B5C4)3 does not have glass formation ability.\\n\"\n    }\n]"
  },
  {
    "path": "dataset/matbench_is_metal/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 1,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('matbench_is_metal.csv')\\n\",\n    \"# key=csv column name, value=slot in Q\\n\",\n    \"slot = {\\\"composition\\\":\\\"composition\\\"}\\n\",\n    \"data_list = []\\n\",\n    \"for s in slot.keys():\\n\",\n    \"    for i, element in enumerate(df[s]):\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,2)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"Is composition metal? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Is given composition metal? ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given composition, is it metal? ->\\\"\\n\",\n    \"        answer = df['is metal?'][i]\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] =  \\\" \\\"+ element +\\\"\\\\n\\\"\\n\",\n    \"        if answer == True:\\n\",\n    \"            tmp_dict[\\\"output\\\"] = f\\\" Yes, {element} is metal.\\\\n\\\"\\n\",\n    \"        elif answer == False:\\n\",\n    \"            tmp_dict[\\\"output\\\"] = f\\\" No, {element} is not metal.\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 2,\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"data\": {\n      \"text/plain\": [\n       \"[{'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag(AuS)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ag(AuS)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag(W3Br7)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ag(W3Br7)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag0.5Ge1Pb1.75S4\\\\n',\\n\",\n       \"  'output': ' No, Ag0.5Ge1Pb1.75S4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag0.5Ge1Pb1.75Se4\\\\n',\\n\",\n       \"  'output': ' No, Ag0.5Ge1Pb1.75Se4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag2BBr\\\\n',\\n\",\n       \"  'output': ' Yes, Ag2BBr is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag2BiO3\\\\n',\\n\",\n       \"  'output': ' Yes, Ag2BiO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag2GeS3\\\\n',\\n\",\n       \"  'output': ' No, Ag2GeS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag2GeSe3\\\\n',\\n\",\n       \"  'output': ' No, Ag2GeSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag2GeTe3\\\\n',\\n\",\n       \"  'output': ' No, Ag2GeTe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag2HgI4\\\\n',\\n\",\n       \"  'output': ' No, Ag2HgI4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag2Mo(I2O7)2\\\\n',\\n\",\n       \"  'output': ' No, Ag2Mo(I2O7)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag2O\\\\n',\\n\",\n       \"  'output': ' No, Ag2O is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag2P2PbO7\\\\n',\\n\",\n       \"  'output': ' Yes, Ag2P2PbO7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag2PdO2\\\\n',\\n\",\n       \"  'output': ' No, Ag2PdO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag2S\\\\n',\\n\",\n       \"  'output': ' No, Ag2S is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag2SnS3\\\\n',\\n\",\n       \"  'output': ' No, Ag2SnS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag2SnSe3\\\\n',\\n\",\n       \"  'output': ' No, Ag2SnSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag3AsO4\\\\n',\\n\",\n       \"  'output': ' Yes, Ag3AsO4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag3AsS3\\\\n',\\n\",\n       \"  'output': ' No, Ag3AsS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag3AsSe3\\\\n',\\n\",\n       \"  'output': ' No, Ag3AsSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag3Pd\\\\n',\\n\",\n       \"  'output': ' Yes, Ag3Pd is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag3RuO4\\\\n',\\n\",\n       \"  'output': ' Yes, Ag3RuO4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag3SbS3\\\\n',\\n\",\n       \"  'output': ' No, Ag3SbS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ag5IO6\\\\n',\\n\",\n       \"  'output': ' No, Ag5IO6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag7(SI)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ag7(SI)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag7AsS6\\\\n',\\n\",\n       \"  'output': ' No, Ag7AsS6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag7AsSe6\\\\n',\\n\",\n       \"  'output': ' No, Ag7AsSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag7NO11\\\\n',\\n\",\n       \"  'output': ' Yes, Ag7NO11 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag8GeS6\\\\n',\\n\",\n       \"  'output': ' No, Ag8GeS6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ag8SnSe6\\\\n',\\n\",\n       \"  'output': ' No, Ag8SnSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag9(PbO3)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ag9(PbO3)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ag9Ge2IO8\\\\n',\\n\",\n       \"  'output': ' Yes, Ag9Ge2IO8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgAsS2\\\\n',\\n\",\n       \"  'output': ' No, AgAsS2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgAsSe2\\\\n',\\n\",\n       \"  'output': ' No, AgAsSe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgAu3\\\\n',\\n\",\n       \"  'output': ' Yes, AgAu3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgBi(PS3)2\\\\n',\\n\",\n       \"  'output': ' No, AgBi(PS3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgBi(PSe3)2\\\\n',\\n\",\n       \"  'output': ' No, AgBi(PSe3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgBiPbS3\\\\n',\\n\",\n       \"  'output': ' No, AgBiPbS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgBiPbSe3\\\\n',\\n\",\n       \"  'output': ' No, AgBiPbSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgBiS2\\\\n',\\n\",\n       \"  'output': ' No, AgBiS2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgBiSe2\\\\n',\\n\",\n       \"  'output': ' No, AgBiSe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgBr\\\\n',\\n\",\n       \"  'output': ' No, AgBr is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgCNO\\\\n',\\n\",\n       \"  'output': ' Yes, AgCNO is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgCl\\\\n',\\n\",\n       \"  'output': ' No, AgCl is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgF\\\\n',\\n\",\n       \"  'output': ' No, AgF is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgGeO3\\\\n',\\n\",\n       \"  'output': ' Yes, AgGeO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgI\\\\n',\\n\",\n       \"  'output': ' No, AgI is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgN3\\\\n',\\n\",\n       \"  'output': ' No, AgN3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgO\\\\n',\\n\",\n       \"  'output': ' No, AgO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgP15\\\\n',\\n\",\n       \"  'output': ' No, AgP15 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgPd(IO3)3\\\\n',\\n\",\n       \"  'output': ' No, AgPd(IO3)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgPdO2\\\\n',\\n\",\n       \"  'output': ' Yes, AgPdO2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgPt3\\\\n',\\n\",\n       \"  'output': ' Yes, AgPt3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgS\\\\n',\\n\",\n       \"  'output': ' No, AgS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgSO4\\\\n',\\n\",\n       \"  'output': ' No, AgSO4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AgSbS2\\\\n',\\n\",\n       \"  'output': ' No, AgSbS2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgSbSe2\\\\n',\\n\",\n       \"  'output': ' No, AgSbSe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgSbTe2\\\\n',\\n\",\n       \"  'output': ' No, AgSbTe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AgTe\\\\n',\\n\",\n       \"  'output': ' No, AgTe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AgTe2As\\\\n',\\n\",\n       \"  'output': ' No, AgTe2As is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al(Ni10B7)2\\\\n',\\n\",\n       \"  'output': ' Yes, Al(Ni10B7)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al(NiS2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Al(NiS2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.01Cd0.99Sb0.01Te0.99\\\\n',\\n\",\n       \"  'output': ' No, Al0.01Cd0.99Sb0.01Te0.99 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.01Ga0.99P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.01Ga0.99P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.01In0.99P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.01In0.99P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.05Cd0.95Sb0.05Te0.95\\\\n',\\n\",\n       \"  'output': ' No, Al0.05Cd0.95Sb0.05Te0.95 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.15Ga0.85As1\\\\n',\\n\",\n       \"  'output': ' No, Al0.15Ga0.85As1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.1Cd0.9Sb0.1Te0.9\\\\n',\\n\",\n       \"  'output': ' No, Al0.1Cd0.9Sb0.1Te0.9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al0.1In0.9P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.1In0.9P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.2Ga0.8P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.2Ga0.8P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.2In0.8P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.2In0.8P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.35Ga0.65As1\\\\n',\\n\",\n       \"  'output': ' No, Al0.35Ga0.65As1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.3Ga0.7As1\\\\n',\\n\",\n       \"  'output': ' No, Al0.3Ga0.7As1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.3In0.7P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.3In0.7P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al0.45Cd0.55Sb0.45Te0.55\\\\n',\\n\",\n       \"  'output': ' No, Al0.45Cd0.55Sb0.45Te0.55 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al0.4Cd0.6Sb0.4Te0.6\\\\n',\\n\",\n       \"  'output': ' No, Al0.4Cd0.6Sb0.4Te0.6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.4Ga0.6P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.4Ga0.6P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al0.4In0.6P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.4In0.6P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.5Ga0.5As1\\\\n',\\n\",\n       \"  'output': ' No, Al0.5Ga0.5As1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.5In0.5P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.5In0.5P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.6Ga0.4As1\\\\n',\\n\",\n       \"  'output': ' No, Al0.6Ga0.4As1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al0.6Ga0.4P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.6Ga0.4P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.6In0.4P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.6In0.4P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al0.75Ga0.25As1\\\\n',\\n\",\n       \"  'output': ' No, Al0.75Ga0.25As1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.7In0.3P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.7In0.3P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al0.8Ga0.2P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.8Ga0.2P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al0.99Cd0.01Sb0.99Te0.01\\\\n',\\n\",\n       \"  'output': ' No, Al0.99Cd0.01Sb0.99Te0.01 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.99Ga0.01P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.99Ga0.01P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al0.99In0.01P1\\\\n',\\n\",\n       \"  'output': ' No, Al0.99In0.01P1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al10V\\\\n',\\n\",\n       \"  'output': ' Yes, Al10V is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al13Ru4\\\\n',\\n\",\n       \"  'output': ' Yes, Al13Ru4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al2(CuSe2)3\\\\n',\\n\",\n       \"  'output': ' Yes, Al2(CuSe2)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al21Pt8\\\\n',\\n\",\n       \"  'output': ' Yes, Al21Pt8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al2CoIr\\\\n',\\n\",\n       \"  'output': ' Yes, Al2CoIr is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al2Cr2O7\\\\n',\\n\",\n       \"  'output': ' Yes, Al2Cr2O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al2CrS4\\\\n',\\n\",\n       \"  'output': ' Yes, Al2CrS4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al2Cu\\\\n',\\n\",\n       \"  'output': ' Yes, Al2Cu is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al2FeNi\\\\n',\\n\",\n       \"  'output': ' Yes, Al2FeNi is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al2Ru\\\\n',\\n\",\n       \"  'output': ' Yes, Al2Ru is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al2S3\\\\n',\\n\",\n       \"  'output': ' No, Al2S3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al2Se3\\\\n',\\n\",\n       \"  'output': ' No, Al2Se3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al2Te3\\\\n',\\n\",\n       \"  'output': ' No, Al2Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al3Tc\\\\n',\\n\",\n       \"  'output': ' Yes, Al3Tc is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al4Cu2O7\\\\n',\\n\",\n       \"  'output': ' Yes, Al4Cu2O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Al4Cu9\\\\n',\\n\",\n       \"  'output': ' Yes, Al4Cu9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al5Rh2\\\\n',\\n\",\n       \"  'output': ' Yes, Al5Rh2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al6Fe\\\\n',\\n\",\n       \"  'output': ' Yes, Al6Fe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al6Ru\\\\n',\\n\",\n       \"  'output': ' Yes, Al6Ru is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al6Tc\\\\n',\\n\",\n       \"  'output': ' Yes, Al6Tc is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al7(CN)3\\\\n',\\n\",\n       \"  'output': ' Yes, Al7(CN)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al9Co2\\\\n',\\n\",\n       \"  'output': ' Yes, Al9Co2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Al9Ir2\\\\n',\\n\",\n       \"  'output': ' Yes, Al9Ir2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Al9Rh2\\\\n',\\n\",\n       \"  'output': ' Yes, Al9Rh2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlAgO2\\\\n',\\n\",\n       \"  'output': ' No, AlAgO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AlAgS2\\\\n',\\n\",\n       \"  'output': ' No, AlAgS2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlAgSe2\\\\n',\\n\",\n       \"  'output': ' No, AlAgSe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlAgTe2\\\\n',\\n\",\n       \"  'output': ' No, AlAgTe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlAs\\\\n',\\n\",\n       \"  'output': ' Yes, AlAs is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AlB12\\\\n',\\n\",\n       \"  'output': ' No, AlB12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlB2\\\\n',\\n\",\n       \"  'output': ' Yes, AlB2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlBi\\\\n',\\n\",\n       \"  'output': ' No, AlBi is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlCoO3\\\\n',\\n\",\n       \"  'output': ' Yes, AlCoO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlCu3\\\\n',\\n\",\n       \"  'output': ' Yes, AlCu3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlCu7O12\\\\n',\\n\",\n       \"  'output': ' Yes, AlCu7O12 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlCuS2\\\\n',\\n\",\n       \"  'output': ' No, AlCuS2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlCuSe2\\\\n',\\n\",\n       \"  'output': ' No, AlCuSe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlCuTe2\\\\n',\\n\",\n       \"  'output': ' No, AlCuTe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlFe2Si\\\\n',\\n\",\n       \"  'output': ' Yes, AlFe2Si is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlFe4(CuO4)3\\\\n',\\n\",\n       \"  'output': ' Yes, AlFe4(CuO4)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlIr\\\\n',\\n\",\n       \"  'output': ' Yes, AlIr is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlN\\\\n',\\n\",\n       \"  'output': ' No, AlN is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AlNi2\\\\n',\\n\",\n       \"  'output': ' Yes, AlNi2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AlP\\\\n',\\n\",\n       \"  'output': ' No, AlP is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlPd5I2\\\\n',\\n\",\n       \"  'output': ' Yes, AlPd5I2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlSb\\\\n',\\n\",\n       \"  'output': ' No, AlSb is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AlSn\\\\n',\\n\",\n       \"  'output': ' Yes, AlSn is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AlV(TeO4)2\\\\n',\\n\",\n       \"  'output': ' No, AlV(TeO4)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AlVCo2\\\\n',\\n\",\n       \"  'output': ' Yes, AlVCo2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' As2Ir\\\\n',\\n\",\n       \"  'output': ' No, As2Ir is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' As2O3\\\\n',\\n\",\n       \"  'output': ' No, As2O3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' As2Os\\\\n',\\n\",\n       \"  'output': ' No, As2Os is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' As2Pt\\\\n',\\n\",\n       \"  'output': ' No, As2Pt is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' As2Rh\\\\n',\\n\",\n       \"  'output': ' No, As2Rh is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' As2Ru\\\\n',\\n\",\n       \"  'output': ' No, As2Ru is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' As2S3\\\\n',\\n\",\n       \"  'output': ' No, As2S3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' As2S5\\\\n',\\n\",\n       \"  'output': ' No, As2S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' As2Se3\\\\n',\\n\",\n       \"  'output': ' No, As2Se3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AsAu3\\\\n',\\n\",\n       \"  'output': ' Yes, AsAu3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AsBr3\\\\n',\\n\",\n       \"  'output': ' No, AsBr3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AsI3\\\\n',\\n\",\n       \"  'output': ' No, AsI3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AsOsS\\\\n',\\n\",\n       \"  'output': ' No, AsOsS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AsP\\\\n',\\n\",\n       \"  'output': ' No, AsP is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AsPPd\\\\n',\\n\",\n       \"  'output': ' No, AsPPd is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AsPPt\\\\n',\\n\",\n       \"  'output': ' No, AsPPt is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AsPRu\\\\n',\\n\",\n       \"  'output': ' No, AsPRu is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' AsPd3Pb2\\\\n',\\n\",\n       \"  'output': ' Yes, AsPd3Pb2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AsRuS\\\\n',\\n\",\n       \"  'output': ' No, AsRuS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AsS\\\\n',\\n\",\n       \"  'output': ' No, AsS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AsS3\\\\n',\\n\",\n       \"  'output': ' No, AsS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AsSI\\\\n',\\n\",\n       \"  'output': ' No, AsSI is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AsSeBr\\\\n',\\n\",\n       \"  'output': ' Yes, AsSeBr is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' AsSeI\\\\n',\\n\",\n       \"  'output': ' No, AsSeI is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Au3S\\\\n',\\n\",\n       \"  'output': ' Yes, Au3S is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' AuBrO2\\\\n',\\n\",\n       \"  'output': ' Yes, AuBrO2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' B2Mo(PbO2)6\\\\n',\\n\",\n       \"  'output': ' No, B2Mo(PbO2)6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' B2O3\\\\n',\\n\",\n       \"  'output': ' No, B2O3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' B2Se2O7\\\\n',\\n\",\n       \"  'output': ' No, B2Se2O7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' B3H2Pb2O7.5\\\\n',\\n\",\n       \"  'output': ' No, B3H2Pb2O7.5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' B3Pb10Br3O13\\\\n',\\n\",\n       \"  'output': ' No, B3Pb10Br3O13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' B3Pb3NO10\\\\n',\\n\",\n       \"  'output': ' No, B3Pb3NO10 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' B4C\\\\n',\\n\",\n       \"  'output': ' No, B4C is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' B4H2Pb6O13\\\\n',\\n\",\n       \"  'output': ' No, B4H2Pb6O13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' B4W\\\\n',\\n\",\n       \"  'output': ' Yes, B4W is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' B5Mo2\\\\n',\\n\",\n       \"  'output': ' Yes, B5Mo2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' B6As\\\\n',\\n\",\n       \"  'output': ' No, B6As is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' B6P\\\\n',\\n\",\n       \"  'output': ' No, B6P is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BAs\\\\n',\\n\",\n       \"  'output': ' No, BAs is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BH(PbO2)2\\\\n',\\n\",\n       \"  'output': ' No, BH(PbO2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BMo\\\\n',\\n\",\n       \"  'output': ' Yes, BMo is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BP\\\\n',\\n\",\n       \"  'output': ' No, BP is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BPb2ClO3\\\\n',\\n\",\n       \"  'output': ' No, BPb2ClO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BPb6BrO7\\\\n',\\n\",\n       \"  'output': ' No, BPb6BrO7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BPb7Br3O7\\\\n',\\n\",\n       \"  'output': ' No, BPb7Br3O7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BRh2\\\\n',\\n\",\n       \"  'output': ' Yes, BRh2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BSb\\\\n',\\n\",\n       \"  'output': ' No, BSb is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BSbPbS4\\\\n',\\n\",\n       \"  'output': ' No, BSbPbS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BSe2Cl\\\\n',\\n\",\n       \"  'output': ' Yes, BSe2Cl is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BTe2As\\\\n',\\n\",\n       \"  'output': ' Yes, BTe2As is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba(AsPd)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba(AsPd)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba(AsRh)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba(AsRh)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba(BO2)2\\\\n',\\n\",\n       \"  'output': ' No, Ba(BO2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba(BRh)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba(BRh)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba(FeS2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba(FeS2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba(GaS2)2\\\\n',\\n\",\n       \"  'output': ' No, Ba(GaS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba(GaSe2)2\\\\n',\\n\",\n       \"  'output': ' No, Ba(GaSe2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba(InS2)2\\\\n',\\n\",\n       \"  'output': ' No, Ba(InS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba(InSe2)2\\\\n',\\n\",\n       \"  'output': ' No, Ba(InSe2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba(NiP2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba(NiP2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba(PdO2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba(PdO2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba(SnO2)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ba(SnO2)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba(ZnAs)2\\\\n',\\n\",\n       \"  'output': ' No, Ba(ZnAs)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba1.88Ta15O32\\\\n',\\n\",\n       \"  'output': ' No, Ba1.88Ta15O32 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba12In4S19\\\\n',\\n\",\n       \"  'output': ' No, Ba12In4S19 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba14Ir8(PdO11)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ba14Ir8(PdO11)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba14Na8CaN6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba14Na8CaN6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba23Ga8(SbS19)2\\\\n',\\n\",\n       \"  'output': ' No, Ba23Ga8(SbS19)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2B4H2O9\\\\n',\\n\",\n       \"  'output': ' No, Ba2B4H2O9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2B6H4O13\\\\n',\\n\",\n       \"  'output': ' No, Ba2B6H4O13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2B6O11\\\\n',\\n\",\n       \"  'output': ' No, Ba2B6O11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2BiSbO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2BiSbO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2CaOsO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2CaOsO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2CaReO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2CaReO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2Cd(BO2)6\\\\n',\\n\",\n       \"  'output': ' No, Ba2Cd(BO2)6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2Ce2O5\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2Ce2O5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2CeInTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2CeInTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2CoWO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2CoWO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2Cu5F14\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2Cu5F14 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2CuWO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2CuWO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2DyCu3O7\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2DyCu3O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2DyGaSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2DyGaSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2DyGaTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2DyGaTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2DyInSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2DyInSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2DyInTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2DyInTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2ErGaSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2ErGaSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2ErGaTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2ErGaTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2ErInSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2ErInSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2ErInTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2ErInTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2FeMoO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2FeMoO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2FeReO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2FeReO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2Ga8GeS16\\\\n',\\n\",\n       \"  'output': ' No, Ba2Ga8GeS16 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2Ga8SiS16\\\\n',\\n\",\n       \"  'output': ' No, Ba2Ga8SiS16 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2GaAsSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaAsSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2GaBiS5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaBiS5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2GaBiSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaBiSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2GaBiTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaBiTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2GaS4\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2GaSbSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaSbSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2GaSbTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaSbTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2GaSe4\\\\n',\\n\",\n       \"  'output': ' No, Ba2GaSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2GdGaSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GdGaSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2GdGaTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GdGaTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2GdInSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GdInSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2GdInTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2GdInTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2HgS5\\\\n',\\n\",\n       \"  'output': ' No, Ba2HgS5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2In2S5\\\\n',\\n\",\n       \"  'output': ' No, Ba2In2S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2In2Se5\\\\n',\\n\",\n       \"  'output': ' No, Ba2In2Se5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2InAgS4\\\\n',\\n\",\n       \"  'output': ' No, Ba2InAgS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2InBiS5\\\\n',\\n\",\n       \"  'output': ' No, Ba2InBiS5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2InSbSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2InSbSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2LaIrO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2LaIrO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2LiFe2N3\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2LiFe2N3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2NaCu3S5\\\\n',\\n\",\n       \"  'output': ' No, Ba2NaCu3S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2NdGaS5\\\\n',\\n\",\n       \"  'output': ' No, Ba2NdGaS5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2NdGaSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2NdGaSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2NdInSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2NdInSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2NdInTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2NdInTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2ReNiO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2ReNiO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2Sb7HO14\\\\n',\\n\",\n       \"  'output': ' No, Ba2Sb7HO14 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2ScIrO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2ScIrO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2ScTaO6\\\\n',\\n\",\n       \"  'output': ' No, Ba2ScTaO6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2SmCu3O7\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2SmCu3O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2SmGaSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2SmGaSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2SmGaTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2SmGaTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2SmInSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2SmInSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2SmInTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2SmInTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2SmTaO6\\\\n',\\n\",\n       \"  'output': ' No, Ba2SmTaO6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2SnSe4\\\\n',\\n\",\n       \"  'output': ' No, Ba2SnSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2SnSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2SnSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2TaInO6\\\\n',\\n\",\n       \"  'output': ' No, Ba2TaInO6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2TbIrO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2TbIrO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2ThCu2Se5\\\\n',\\n\",\n       \"  'output': ' No, Ba2ThCu2Se5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2UCuO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2UCuO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2V2Te2O11\\\\n',\\n\",\n       \"  'output': ' No, Ba2V2Te2O11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2V2ZnO8\\\\n',\\n\",\n       \"  'output': ' No, Ba2V2ZnO8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2V4(TeO6)3\\\\n',\\n\",\n       \"  'output': ' No, Ba2V4(TeO6)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2YGaSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2YGaSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2YGaTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2YGaTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2YInSe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2YInSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2YInTe5\\\\n',\\n\",\n       \"  'output': ' No, Ba2YInTe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2YReO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2YReO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba2Yb(CuO2)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ba2Yb(CuO2)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba2Zn0.2B2S5.2\\\\n',\\n\",\n       \"  'output': ' No, Ba2Zn0.2B2S5.2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2ZnSe3\\\\n',\\n\",\n       \"  'output': ' No, Ba2ZnSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba2ZnTe3\\\\n',\\n\",\n       \"  'output': ' No, Ba2ZnTe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3(AlGe)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3(AlGe)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3(LiSn2)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3(LiSn2)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3Ag2(SnS4)2\\\\n',\\n\",\n       \"  'output': ' No, Ba3Ag2(SnS4)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3B1.5Sb0.5S6\\\\n',\\n\",\n       \"  'output': ' No, Ba3B1.5Sb0.5S6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3BSbS6\\\\n',\\n\",\n       \"  'output': ' No, Ba3BSbS6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3BSbSe6\\\\n',\\n\",\n       \"  'output': ' No, Ba3BSbSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3Bi0.5B1.5S6\\\\n',\\n\",\n       \"  'output': ' No, Ba3Bi0.5B1.5S6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3Bi2TeO9\\\\n',\\n\",\n       \"  'output': ' No, Ba3Bi2TeO9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3CaIr2O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3CaIr2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3CaRu2O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3CaRu2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3Cd(SnS4)2\\\\n',\\n\",\n       \"  'output': ' No, Ba3Cd(SnS4)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3Co10O17\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3Co10O17 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3CrS5\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3CrS5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Dy2(PS4)4\\\\n',\\n\",\n       \"  'output': ' No, Ba3Dy2(PS4)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Er2(PS4)4\\\\n',\\n\",\n       \"  'output': ' No, Ba3Er2(PS4)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3ErRu2O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3ErRu2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3Eu(PO4)3\\\\n',\\n\",\n       \"  'output': ' No, Ba3Eu(PO4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3FeS4Br\\\\n',\\n\",\n       \"  'output': ' No, Ba3FeS4Br is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3Gd2(PS4)4\\\\n',\\n\",\n       \"  'output': ' No, Ba3Gd2(PS4)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3GeS5\\\\n',\\n\",\n       \"  'output': ' No, Ba3GeS5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3Ho2(PS4)4\\\\n',\\n\",\n       \"  'output': ' No, Ba3Ho2(PS4)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3In2(PO4)4\\\\n',\\n\",\n       \"  'output': ' No, Ba3In2(PO4)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3InS4Cl\\\\n',\\n\",\n       \"  'output': ' No, Ba3InS4Cl is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3La3(Cu3O7)2\\\\n',\\n\",\n       \"  'output': ' No, Ba3La3(Cu3O7)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3MgTa2O9\\\\n',\\n\",\n       \"  'output': ' No, Ba3MgTa2O9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3N2\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3N2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3NaIr2O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3NaIr2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3NaIrO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3NaIrO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Nb2CoO9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3Nb2CoO9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3Nb2Se9\\\\n',\\n\",\n       \"  'output': ' No, Ba3Nb2Se9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba3P3ClO10\\\\n',\\n\",\n       \"  'output': ' No, Ba3P3ClO10 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3PN\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3PN is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Sb2S7\\\\n',\\n\",\n       \"  'output': ' No, Ba3Sb2S7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Sn(SbSe4)2\\\\n',\\n\",\n       \"  'output': ' No, Ba3Sn(SbSe4)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3Sn0.87Bi2.13Se8\\\\n',\\n\",\n       \"  'output': ' No, Ba3Sn0.87Bi2.13Se8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Ta2Se9\\\\n',\\n\",\n       \"  'output': ' No, Ba3Ta2Se9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Ta2ZnO9\\\\n',\\n\",\n       \"  'output': ' No, Ba3Ta2ZnO9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Ta5NO14\\\\n',\\n\",\n       \"  'output': ' No, Ba3Ta5NO14 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3Tb2(PS4)4\\\\n',\\n\",\n       \"  'output': ' No, Ba3Tb2(PS4)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3Te\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3Te is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba3ThSe7\\\\n',\\n\",\n       \"  'output': ' No, Ba3ThSe7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3V2(SeO4)4\\\\n',\\n\",\n       \"  'output': ' No, Ba3V2(SeO4)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3YIr2O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3YIr2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3Yb4O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3Yb4O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba3ZrRu2O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba3ZrRu2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba4B11O20F\\\\n',\\n\",\n       \"  'output': ' No, Ba4B11O20F is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4Ga4GeSe12\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ga4GeSe12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba4Ga4SnSe12\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ga4SnSe12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba4Ga5AgS12\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ga5AgS12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba4Ga5CuS12\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ga5CuS12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba4Ga5CuSe12\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ga5CuSe12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4Ga5Si18\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ga5Si18 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba4Ge3S9Cl2\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ge3S9Cl2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4Ge3Se9Cl2\\\\n',\\n\",\n       \"  'output': ' No, Ba4Ge3Se9Cl2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba4InAgSe6\\\\n',\\n\",\n       \"  'output': ' No, Ba4InAgSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba4InCuSe6\\\\n',\\n\",\n       \"  'output': ' No, Ba4InCuSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4LiGa5Se12\\\\n',\\n\",\n       \"  'output': ' No, Ba4LiGa5Se12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4Nb14O23\\\\n',\\n\",\n       \"  'output': ' Yes, Ba4Nb14O23 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4Sb3S8Cl\\\\n',\\n\",\n       \"  'output': ' No, Ba4Sb3S8Cl is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4Si20Au3\\\\n',\\n\",\n       \"  'output': ' Yes, Ba4Si20Au3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba4Si3Se9Cl2\\\\n',\\n\",\n       \"  'output': ' No, Ba4Si3Se9Cl2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba4Sm2Cu2O9\\\\n',\\n\",\n       \"  'output': ' Yes, Ba4Sm2Cu2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba4Yb(CuO3)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ba4Yb(CuO3)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba5(Ga2Se5)2\\\\n',\\n\",\n       \"  'output': ' No, Ba5(Ga2Se5)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba5(GaSe4)2\\\\n',\\n\",\n       \"  'output': ' No, Ba5(GaSe4)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba5Al2Ge7\\\\n',\\n\",\n       \"  'output': ' Yes, Ba5Al2Ge7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba5Bi3\\\\n',\\n\",\n       \"  'output': ' Yes, Ba5Bi3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba5Cd(Ga2Se5)3\\\\n',\\n\",\n       \"  'output': ' No, Ba5Cd(Ga2Se5)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba5Ga6GeP12\\\\n',\\n\",\n       \"  'output': ' No, Ba5Ga6GeP12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba5Ga6SnP12\\\\n',\\n\",\n       \"  'output': ' No, Ba5Ga6SnP12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba5Ge3\\\\n',\\n\",\n       \"  'output': ' Yes, Ba5Ge3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba5In4Bi5\\\\n',\\n\",\n       \"  'output': ' Yes, Ba5In4Bi5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba5In4Te4S7\\\\n',\\n\",\n       \"  'output': ' No, Ba5In4Te4S7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba5Sb3\\\\n',\\n\",\n       \"  'output': ' Yes, Ba5Sb3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba5V3O12F\\\\n',\\n\",\n       \"  'output': ' No, Ba5V3O12F is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba6Ag2.7Sn4.3S16\\\\n',\\n\",\n       \"  'output': ' No, Ba6Ag2.7Sn4.3S16 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba6Al4B14O33\\\\n',\\n\",\n       \"  'output': ' No, Ba6Al4B14O33 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba6Ga2SnSe11\\\\n',\\n\",\n       \"  'output': ' No, Ba6Ga2SnSe11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba6In2NF\\\\n',\\n\",\n       \"  'output': ' Yes, Ba6In2NF is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba6Sn6Se13\\\\n',\\n\",\n       \"  'output': ' No, Ba6Sn6Se13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba7(SnS3)5\\\\n',\\n\",\n       \"  'output': ' No, Ba7(SnS3)5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba7B3O9F5\\\\n',\\n\",\n       \"  'output': ' No, Ba7B3O9F5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba7Ga5AgS15\\\\n',\\n\",\n       \"  'output': ' No, Ba7Ga5AgS15 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ba7Ru4Br2O15\\\\n',\\n\",\n       \"  'output': ' Yes, Ba7Ru4Br2O15 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba8Al10B12O41\\\\n',\\n\",\n       \"  'output': ' No, Ba8Al10B12O41 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ba8Hg4Se7S5\\\\n',\\n\",\n       \"  'output': ' No, Ba8Hg4Se7S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba8Sn4S15\\\\n',\\n\",\n       \"  'output': ' No, Ba8Sn4S15 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ba8Ta7O24\\\\n',\\n\",\n       \"  'output': ' Yes, Ba8Ta7O24 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaAg\\\\n',\\n\",\n       \"  'output': ' Yes, BaAg is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaAg2\\\\n',\\n\",\n       \"  'output': ' Yes, BaAg2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaAgSbS3\\\\n',\\n\",\n       \"  'output': ' No, BaAgSbS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaAl2\\\\n',\\n\",\n       \"  'output': ' Yes, BaAl2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaAl4Se7\\\\n',\\n\",\n       \"  'output': ' No, BaAl4Se7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaAlCu4O7\\\\n',\\n\",\n       \"  'output': ' Yes, BaAlCu4O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaAu(IO3)5\\\\n',\\n\",\n       \"  'output': ' No, BaAu(IO3)5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaAu2\\\\n',\\n\",\n       \"  'output': ' Yes, BaAu2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaB6\\\\n',\\n\",\n       \"  'output': ' No, BaB6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaBClF4\\\\n',\\n\",\n       \"  'output': ' No, BaBClF4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaBSbS4\\\\n',\\n\",\n       \"  'output': ' No, BaBSbS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaBiClO2\\\\n',\\n\",\n       \"  'output': ' No, BaBiClO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaCaB2O5\\\\n',\\n\",\n       \"  'output': ' No, BaCaB2O5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaCaSn3\\\\n',\\n\",\n       \"  'output': ' Yes, BaCaSn3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaCdSnS4\\\\n',\\n\",\n       \"  'output': ' No, BaCdSnS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaCu2SnSe4\\\\n',\\n\",\n       \"  'output': ' No, BaCu2SnSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaCuSbS3\\\\n',\\n\",\n       \"  'output': ' No, BaCuSbS3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaCuSbSe3\\\\n',\\n\",\n       \"  'output': ' No, BaCuSbSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaCuTeF\\\\n',\\n\",\n       \"  'output': ' No, BaCuTeF is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaDy2CuO5\\\\n',\\n\",\n       \"  'output': ' Yes, BaDy2CuO5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaEu2Mn2O7\\\\n',\\n\",\n       \"  'output': ' Yes, BaEu2Mn2O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaF2\\\\n',\\n\",\n       \"  'output': ' No, BaF2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGa2GeS6\\\\n',\\n\",\n       \"  'output': ' No, BaGa2GeS6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGa2GeSe6\\\\n',\\n\",\n       \"  'output': ' No, BaGa2GeSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGa2SiS6\\\\n',\\n\",\n       \"  'output': ' No, BaGa2SiS6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGa2SiSe6\\\\n',\\n\",\n       \"  'output': ' No, BaGa2SiSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGa2SnSe6\\\\n',\\n\",\n       \"  'output': ' No, BaGa2SnSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGa4S7\\\\n',\\n\",\n       \"  'output': ' No, BaGa4S7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGa4Se7\\\\n',\\n\",\n       \"  'output': ' No, BaGa4Se7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGe2\\\\n',\\n\",\n       \"  'output': ' No, BaGe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaGe3Pt\\\\n',\\n\",\n       \"  'output': ' Yes, BaGe3Pt is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaGe4(IrS3)2\\\\n',\\n\",\n       \"  'output': ' No, BaGe4(IrS3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGe4(IrSe3)2\\\\n',\\n\",\n       \"  'output': ' No, BaGe4(IrSe3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaGe4(RhSe3)2\\\\n',\\n\",\n       \"  'output': ' No, BaGe4(RhSe3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaHgS2\\\\n',\\n\",\n       \"  'output': ' No, BaHgS2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaHgSe2\\\\n',\\n\",\n       \"  'output': ' No, BaHgSe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaIn2(P2O7)2\\\\n',\\n\",\n       \"  'output': ' No, BaIn2(P2O7)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaIn2Ir\\\\n',\\n\",\n       \"  'output': ' Yes, BaIn2Ir is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaLa2CoS5\\\\n',\\n\",\n       \"  'output': ' Yes, BaLa2CoS5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaLa2In2S7\\\\n',\\n\",\n       \"  'output': ' No, BaLa2In2S7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaLa2In2Se7\\\\n',\\n\",\n       \"  'output': ' No, BaLa2In2Se7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaLa2Te5O14\\\\n',\\n\",\n       \"  'output': ' No, BaLa2Te5O14 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaLi4\\\\n',\\n\",\n       \"  'output': ' Yes, BaLi4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaMn4O7\\\\n',\\n\",\n       \"  'output': ' Yes, BaMn4O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaMn4ZnO8\\\\n',\\n\",\n       \"  'output': ' Yes, BaMn4ZnO8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaMnO3\\\\n',\\n\",\n       \"  'output': ' Yes, BaMnO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaNa2GeS4\\\\n',\\n\",\n       \"  'output': ' No, BaNa2GeS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaNa2GeSe4\\\\n',\\n\",\n       \"  'output': ' No, BaNa2GeSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaNa2SnS4\\\\n',\\n\",\n       \"  'output': ' No, BaNa2SnS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaNa2SnSe4\\\\n',\\n\",\n       \"  'output': ' No, BaNa2SnSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaNaB5O9\\\\n',\\n\",\n       \"  'output': ' No, BaNaB5O9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaNb4O6\\\\n',\\n\",\n       \"  'output': ' Yes, BaNb4O6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaO\\\\n',\\n\",\n       \"  'output': ' No, BaO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaPd(IO3)4\\\\n',\\n\",\n       \"  'output': ' No, BaPd(IO3)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaPdSe6\\\\n',\\n\",\n       \"  'output': ' No, BaPdSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaPrO3\\\\n',\\n\",\n       \"  'output': ' No, BaPrO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaPt5\\\\n',\\n\",\n       \"  'output': ' Yes, BaPt5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaReH9\\\\n',\\n\",\n       \"  'output': ' No, BaReH9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaS\\\\n',\\n\",\n       \"  'output': ' No, BaS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaSe\\\\n',\\n\",\n       \"  'output': ' No, BaSe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaSi\\\\n',\\n\",\n       \"  'output': ' Yes, BaSi is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaSi2\\\\n',\\n\",\n       \"  'output': ' No, BaSi2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaSn2S5\\\\n',\\n\",\n       \"  'output': ' No, BaSn2S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaSn3\\\\n',\\n\",\n       \"  'output': ' Yes, BaSn3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaSnO3\\\\n',\\n\",\n       \"  'output': ' No, BaSnO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaTaNO2\\\\n',\\n\",\n       \"  'output': ' No, BaTaNO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaTbMn2O6\\\\n',\\n\",\n       \"  'output': ' Yes, BaTbMn2O6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaTe\\\\n',\\n\",\n       \"  'output': ' No, BaTe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaTeMo2O9\\\\n',\\n\",\n       \"  'output': ' No, BaTeMo2O9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaTh3\\\\n',\\n\",\n       \"  'output': ' Yes, BaTh3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaTi14O28\\\\n',\\n\",\n       \"  'output': ' Yes, BaTi14O28 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaTi4O7\\\\n',\\n\",\n       \"  'output': ' Yes, BaTi4O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaTi4O8\\\\n',\\n\",\n       \"  'output': ' Yes, BaTi4O8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaTiO3\\\\n',\\n\",\n       \"  'output': ' No, BaTiO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaTl(MoO3)2\\\\n',\\n\",\n       \"  'output': ' Yes, BaTl(MoO3)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaTl3\\\\n',\\n\",\n       \"  'output': ' Yes, BaTl3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaUSe3\\\\n',\\n\",\n       \"  'output': ' No, BaUSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BaV2SeO8\\\\n',\\n\",\n       \"  'output': ' No, BaV2SeO8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaYb2O4\\\\n',\\n\",\n       \"  'output': ' Yes, BaYb2O4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaYbSn3\\\\n',\\n\",\n       \"  'output': ' Yes, BaYbSn3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaZn(MoO2)4\\\\n',\\n\",\n       \"  'output': ' Yes, BaZn(MoO2)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaZn5\\\\n',\\n\",\n       \"  'output': ' Yes, BaZn5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaZnGeSe4\\\\n',\\n\",\n       \"  'output': ' No, BaZnGeSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BaZnSO\\\\n',\\n\",\n       \"  'output': ' No, BaZnSO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BaZnSiSe4\\\\n',\\n\",\n       \"  'output': ' No, BaZnSiSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Be12Pt\\\\n',\\n\",\n       \"  'output': ' Yes, Be12Pt is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Be22Re\\\\n',\\n\",\n       \"  'output': ' Yes, Be22Re is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Be2HgTe\\\\n',\\n\",\n       \"  'output': ' Yes, Be2HgTe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Be2W\\\\n',\\n\",\n       \"  'output': ' Yes, Be2W is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Be3N2\\\\n',\\n\",\n       \"  'output': ' No, Be3N2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Be3Sb2\\\\n',\\n\",\n       \"  'output': ' No, Be3Sb2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BeAlB\\\\n',\\n\",\n       \"  'output': ' Yes, BeAlB is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BeCu\\\\n',\\n\",\n       \"  'output': ' Yes, BeCu is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BeFe2Si\\\\n',\\n\",\n       \"  'output': ' Yes, BeFe2Si is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BeGaO3\\\\n',\\n\",\n       \"  'output': ' Yes, BeGaO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BeGaRh2\\\\n',\\n\",\n       \"  'output': ' Yes, BeGaRh2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BeO\\\\n',\\n\",\n       \"  'output': ' No, BeO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BePd2\\\\n',\\n\",\n       \"  'output': ' Yes, BePd2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BePd3\\\\n',\\n\",\n       \"  'output': ' Yes, BePd3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BeS\\\\n',\\n\",\n       \"  'output': ' No, BeS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BeSe\\\\n',\\n\",\n       \"  'output': ' No, BeSe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BeSiOs2\\\\n',\\n\",\n       \"  'output': ' Yes, BeSiOs2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BeSiRu2\\\\n',\\n\",\n       \"  'output': ' Yes, BeSiRu2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BeTcSe\\\\n',\\n\",\n       \"  'output': ' Yes, BeTcSe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BeTe\\\\n',\\n\",\n       \"  'output': ' No, BeTe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi0.002Te0.003Pb0.999Se0.999\\\\n',\\n\",\n       \"  'output': ' No, Bi0.002Te0.003Pb0.999Se0.999 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi0.04Te0.06Pb0.98Se0.98\\\\n',\\n\",\n       \"  'output': ' No, Bi0.04Te0.06Pb0.98Se0.98 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi0.2Sb1.8Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi0.2Sb1.8Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi0.2Te0.3Pb0.9Se0.9\\\\n',\\n\",\n       \"  'output': ' No, Bi0.2Te0.3Pb0.9Se0.9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi0.4Sb1.6Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi0.4Sb1.6Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi0.4Te0.6Pb0.8Se0.8\\\\n',\\n\",\n       \"  'output': ' No, Bi0.4Te0.6Pb0.8Se0.8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi0.6Sb1.4Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi0.6Sb1.4Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi1.4Sb0.6Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi1.4Sb0.6Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi1.6Sb0.4Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi1.6Sb0.4Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi1.8Sb0.2Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi1.8Sb0.2Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi1.98Sb0.02Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi1.98Sb0.02Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi12PO20\\\\n',\\n\",\n       \"  'output': ' No, Bi12PO20 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi12Rh12O41\\\\n',\\n\",\n       \"  'output': ' Yes, Bi12Rh12O41 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi1Sb0.15\\\\n',\\n\",\n       \"  'output': ' No, Bi1Sb0.15 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi2(BO3)3\\\\n',\\n\",\n       \"  'output': ' Yes, Bi2(BO3)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2(MoO4)3\\\\n',\\n\",\n       \"  'output': ' No, Bi2(MoO4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi2(PO4)3\\\\n',\\n\",\n       \"  'output': ' Yes, Bi2(PO4)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi24BO39\\\\n',\\n\",\n       \"  'output': ' No, Bi24BO39 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2AsClO4\\\\n',\\n\",\n       \"  'output': ' No, Bi2AsClO4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2CO5\\\\n',\\n\",\n       \"  'output': ' No, Bi2CO5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2I4O13\\\\n',\\n\",\n       \"  'output': ' No, Bi2I4O13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Mo2Se2O13\\\\n',\\n\",\n       \"  'output': ' No, Bi2Mo2Se2O13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2O3\\\\n',\\n\",\n       \"  'output': ' No, Bi2O3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2O5\\\\n',\\n\",\n       \"  'output': ' Yes, Bi2O5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Pd3S2\\\\n',\\n\",\n       \"  'output': ' Yes, Bi2Pd3S2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Pt\\\\n',\\n\",\n       \"  'output': ' Yes, Bi2Pt is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2S3\\\\n',\\n\",\n       \"  'output': ' No, Bi2S3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi2SI2O11\\\\n',\\n\",\n       \"  'output': ' No, Bi2SI2O11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Se3\\\\n',\\n\",\n       \"  'output': ' No, Bi2Se3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi2SeI2O11\\\\n',\\n\",\n       \"  'output': ' No, Bi2SeI2O11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te0.03Se2.97\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te0.03Se2.97 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te0.1Se2.9\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te0.1Se2.9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te0.3Se2.7\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te0.3Se2.7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi2Te0.45Se2.55\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te0.45Se2.55 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te0.4Se2.6\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te0.4Se2.6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te0.6Se2.4\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te0.6Se2.4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te0.9Se2.1\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te0.9Se2.1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te1.2Se1.8\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te1.2Se1.8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te1.5Se1.5\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te1.5Se1.5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi2Te2.1Se0.9\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te2.1Se0.9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te2.4Se0.6\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te2.4Se0.6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te2.7Se0.3\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te2.7Se0.3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te2.97Se0.03\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te2.97Se0.03 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te2SO10\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te2SO10 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te2Se\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te2Se is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi2Te3\\\\n',\\n\",\n       \"  'output': ' No, Bi2Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi3BTeO9\\\\n',\\n\",\n       \"  'output': ' No, Bi3BTeO9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi3I4O13F3\\\\n',\\n\",\n       \"  'output': ' No, Bi3I4O13F3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi3Se2NO11\\\\n',\\n\",\n       \"  'output': ' No, Bi3Se2NO11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi4I\\\\n',\\n\",\n       \"  'output': ' Yes, Bi4I is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Bi4Pb7Se13\\\\n',\\n\",\n       \"  'output': ' No, Bi4Pb7Se13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi4Pd(SeO3)4\\\\n',\\n\",\n       \"  'output': ' No, Bi4Pd(SeO3)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Bi5IO7\\\\n',\\n\",\n       \"  'output': ' No, Bi5IO7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi7O5F11\\\\n',\\n\",\n       \"  'output': ' No, Bi7O5F11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi8Te7S5\\\\n',\\n\",\n       \"  'output': ' No, Bi8Te7S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Bi9S6O7.5\\\\n',\\n\",\n       \"  'output': ' No, Bi9S6O7.5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiAs2Os\\\\n',\\n\",\n       \"  'output': ' Yes, BiAs2Os is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiBPbO4\\\\n',\\n\",\n       \"  'output': ' No, BiBPbO4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiBr3\\\\n',\\n\",\n       \"  'output': ' No, BiBr3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiBrO\\\\n',\\n\",\n       \"  'output': ' No, BiBrO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiClO\\\\n',\\n\",\n       \"  'output': ' No, BiClO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiI3\\\\n',\\n\",\n       \"  'output': ' No, BiI3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiIO\\\\n',\\n\",\n       \"  'output': ' No, BiIO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiIO3F2\\\\n',\\n\",\n       \"  'output': ' No, BiIO3F2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiO\\\\n',\\n\",\n       \"  'output': ' Yes, BiO is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiP3(PbO4)3\\\\n',\\n\",\n       \"  'output': ' No, BiP3(PbO4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiPO4\\\\n',\\n\",\n       \"  'output': ' No, BiPO4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiPb2S2I3\\\\n',\\n\",\n       \"  'output': ' No, BiPb2S2I3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BiPbBrO2\\\\n',\\n\",\n       \"  'output': ' No, BiPbBrO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiPbClO2\\\\n',\\n\",\n       \"  'output': ' No, BiPbClO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BiPd\\\\n',\\n\",\n       \"  'output': ' Yes, BiPd is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BiSBr\\\\n',\\n\",\n       \"  'output': ' No, BiSBr is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiSCl\\\\n',\\n\",\n       \"  'output': ' No, BiSCl is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiSI\\\\n',\\n\",\n       \"  'output': ' No, BiSI is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BiSbTe3\\\\n',\\n\",\n       \"  'output': ' No, BiSbTe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiSe\\\\n',\\n\",\n       \"  'output': ' No, BiSe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BiSeBr\\\\n',\\n\",\n       \"  'output': ' No, BiSeBr is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' BiSeI\\\\n',\\n\",\n       \"  'output': ' No, BiSeI is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BiSeO3F\\\\n',\\n\",\n       \"  'output': ' No, BiSeO3F is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' BiTeI\\\\n',\\n\",\n       \"  'output': ' No, BiTeI is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' BiTeNO6\\\\n',\\n\",\n       \"  'output': ' No, BiTeNO6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CBr4\\\\n',\\n\",\n       \"  'output': ' No, CBr4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CI4\\\\n',\\n\",\n       \"  'output': ' No, CI4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca(AgGe)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(AgGe)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca(Al4Co)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(Al4Co)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(AlZn)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(AlZn)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca(BC)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(BC)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(BIr)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(BIr)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca(BiO2)2\\\\n',\\n\",\n       \"  'output': ' No, Ca(BiO2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca(CoGe)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(CoGe)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca(CoS2)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(CoS2)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca(GdS2)2\\\\n',\\n\",\n       \"  'output': ' No, Ca(GdS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(GeRh)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(GeRh)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(LaS2)2\\\\n',\\n\",\n       \"  'output': ' No, Ca(LaS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(MnAs)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(MnAs)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(NdS2)2\\\\n',\\n\",\n       \"  'output': ' No, Ca(NdS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca(Ni2O3)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(Ni2O3)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca(PrS2)2\\\\n',\\n\",\n       \"  'output': ' No, Ca(PrS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca(SiPd)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(SiPd)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(SmS2)2\\\\n',\\n\",\n       \"  'output': ' No, Ca(SmS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca(TiS2)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ca(TiS2)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca10Ge16(B2O17)3\\\\n',\\n\",\n       \"  'output': ' No, Ca10Ge16(B2O17)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca11Bi10\\\\n',\\n\",\n       \"  'output': ' Yes, Ca11Bi10 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca11Ga7\\\\n',\\n\",\n       \"  'output': ' Yes, Ca11Ga7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2Bi2O5\\\\n',\\n\",\n       \"  'output': ' No, Ca2Bi2O5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca2CdAs2\\\\n',\\n\",\n       \"  'output': ' No, Ca2CdAs2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2CdPb\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2CdPb is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2Co9O13\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2Co9O13 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca2CuWO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2CuWO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2Ge\\\\n',\\n\",\n       \"  'output': ' No, Ca2Ge is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2GeN2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2GeN2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2Mn9O13\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2Mn9O13 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2MnAlO5\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2MnAlO5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2NiIrO6\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2NiIrO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2Os2O7\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2Os2O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2PbAu2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2PbAu2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2ScSbO6\\\\n',\\n\",\n       \"  'output': ' No, Ca2ScSbO6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2Si\\\\n',\\n\",\n       \"  'output': ' No, Ca2Si is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2SmTaO6\\\\n',\\n\",\n       \"  'output': ' No, Ca2SmTaO6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca2Sn\\\\n',\\n\",\n       \"  'output': ' No, Ca2Sn is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2Sn2F3\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2Sn2F3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca2SnS4\\\\n',\\n\",\n       \"  'output': ' No, Ca2SnS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca2Ti9O13\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2Ti9O13 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca2TlCd\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2TlCd is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca2ZnRh\\\\n',\\n\",\n       \"  'output': ' Yes, Ca2ZnRh is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3(BN2)2\\\\n',\\n\",\n       \"  'output': ' No, Ca3(BN2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca3(GaPt)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3(GaPt)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca3Al2Ge3\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3Al2Ge3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3Au\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3Au is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca3Au4\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3Au4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca3Bi(PO4)3\\\\n',\\n\",\n       \"  'output': ' No, Ca3Bi(PO4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca3BiAs\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3BiAs is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3BiSb\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3BiSb is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca3Cu2(ClO2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3Cu2(ClO2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3In\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3In is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca3La2(SnS4)3\\\\n',\\n\",\n       \"  'output': ' No, Ca3La2(SnS4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca3N2\\\\n',\\n\",\n       \"  'output': ' No, Ca3N2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca3PbN\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3PbN is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca3Sb2\\\\n',\\n\",\n       \"  'output': ' No, Ca3Sb2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3SbN\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3SbN is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3Sn2S7\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3Sn2S7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3Ti2(SiO4)3\\\\n',\\n\",\n       \"  'output': ' No, Ca3Ti2(SiO4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3TlN\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3TlN is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca3Zr17O37\\\\n',\\n\",\n       \"  'output': ' Yes, Ca3Zr17O37 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca4Al3O10\\\\n',\\n\",\n       \"  'output': ' Yes, Ca4Al3O10 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca4Bi6O13\\\\n',\\n\",\n       \"  'output': ' No, Ca4Bi6O13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca5(Bi7O13)2\\\\n',\\n\",\n       \"  'output': ' No, Ca5(Bi7O13)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca5Au2\\\\n',\\n\",\n       \"  'output': ' Yes, Ca5Au2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca5B3O9F\\\\n',\\n\",\n       \"  'output': ' No, Ca5B3O9F is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca5Ir\\\\n',\\n\",\n       \"  'output': ' Yes, Ca5Ir is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ca5Sb3\\\\n',\\n\",\n       \"  'output': ' Yes, Ca5Sb3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca5Sn4S13\\\\n',\\n\",\n       \"  'output': ' Yes, Ca5Sn4S13 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ca6Ag16N\\\\n',\\n\",\n       \"  'output': ' Yes, Ca6Ag16N is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ca6Cu2Sn7\\\\n',\\n\",\n       \"  'output': ' Yes, Ca6Cu2Sn7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaAgF5\\\\n',\\n\",\n       \"  'output': ' Yes, CaAgF5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaAu5\\\\n',\\n\",\n       \"  'output': ' Yes, CaAu5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaB6\\\\n',\\n\",\n       \"  'output': ' No, CaB6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaCdPd2\\\\n',\\n\",\n       \"  'output': ' Yes, CaCdPd2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaCdSi\\\\n',\\n\",\n       \"  'output': ' Yes, CaCdSi is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaCu5\\\\n',\\n\",\n       \"  'output': ' Yes, CaCu5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaEu2O3\\\\n',\\n\",\n       \"  'output': ' Yes, CaEu2O3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaEuO2\\\\n',\\n\",\n       \"  'output': ' Yes, CaEuO2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaF2\\\\n',\\n\",\n       \"  'output': ' No, CaF2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaGa3Ni2\\\\n',\\n\",\n       \"  'output': ' Yes, CaGa3Ni2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaGaAu3\\\\n',\\n\",\n       \"  'output': ' Yes, CaGaAu3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaGaGe\\\\n',\\n\",\n       \"  'output': ' Yes, CaGaGe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaGe2\\\\n',\\n\",\n       \"  'output': ' Yes, CaGe2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaHfZn\\\\n',\\n\",\n       \"  'output': ' Yes, CaHfZn is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaHg2\\\\n',\\n\",\n       \"  'output': ' Yes, CaHg2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaI2\\\\n',\\n\",\n       \"  'output': ' No, CaI2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaIn2Ir\\\\n',\\n\",\n       \"  'output': ' Yes, CaIn2Ir is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaIn4Ir\\\\n',\\n\",\n       \"  'output': ' Yes, CaIn4Ir is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaInAu\\\\n',\\n\",\n       \"  'output': ' Yes, CaInAu is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaInPt\\\\n',\\n\",\n       \"  'output': ' Yes, CaInPt is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaIrO3\\\\n',\\n\",\n       \"  'output': ' Yes, CaIrO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaMg2N2\\\\n',\\n\",\n       \"  'output': ' No, CaMg2N2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaMgSn\\\\n',\\n\",\n       \"  'output': ' Yes, CaMgSn is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaMnSn\\\\n',\\n\",\n       \"  'output': ' Yes, CaMnSn is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaNi5\\\\n',\\n\",\n       \"  'output': ' Yes, CaNi5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaO\\\\n',\\n\",\n       \"  'output': ' No, CaO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaOsO3\\\\n',\\n\",\n       \"  'output': ' Yes, CaOsO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaPb\\\\n',\\n\",\n       \"  'output': ' Yes, CaPb is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaPd3C\\\\n',\\n\",\n       \"  'output': ' Yes, CaPd3C is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaPrZn2\\\\n',\\n\",\n       \"  'output': ' Yes, CaPrZn2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaS\\\\n',\\n\",\n       \"  'output': ' No, CaS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaSe\\\\n',\\n\",\n       \"  'output': ' No, CaSe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaSnO3\\\\n',\\n\",\n       \"  'output': ' No, CaSnO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaTaNO2\\\\n',\\n\",\n       \"  'output': ' No, CaTaNO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaTe\\\\n',\\n\",\n       \"  'output': ' No, CaTe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CaTi4O8\\\\n',\\n\",\n       \"  'output': ' Yes, CaTi4O8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaTiO2\\\\n',\\n\",\n       \"  'output': ' Yes, CaTiO2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaVO2\\\\n',\\n\",\n       \"  'output': ' Yes, CaVO2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaYbInSe4\\\\n',\\n\",\n       \"  'output': ' Yes, CaYbInSe4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaZn2\\\\n',\\n\",\n       \"  'output': ' Yes, CaZn2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaZn3\\\\n',\\n\",\n       \"  'output': ' Yes, CaZn3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaZn3Ni2\\\\n',\\n\",\n       \"  'output': ' Yes, CaZn3Ni2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CaZn5\\\\n',\\n\",\n       \"  'output': ' Yes, CaZn5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CaZnSO\\\\n',\\n\",\n       \"  'output': ' No, CaZnSO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd(GaS2)2\\\\n',\\n\",\n       \"  'output': ' No, Cd(GaS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd(GaSe2)2\\\\n',\\n\",\n       \"  'output': ' No, Cd(GaSe2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd(In15Te23)2\\\\n',\\n\",\n       \"  'output': ' No, Cd(In15Te23)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd(InS2)2\\\\n',\\n\",\n       \"  'output': ' No, Cd(InS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd(InSe2)2\\\\n',\\n\",\n       \"  'output': ' No, Cd(InSe2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd(InTe2)2\\\\n',\\n\",\n       \"  'output': ' No, Cd(InTe2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd(PS2)2\\\\n',\\n\",\n       \"  'output': ' No, Cd(PS2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.01Ga0.99Sb0.99Te0.01\\\\n',\\n\",\n       \"  'output': ' No, Cd0.01Ga0.99Sb0.99Te0.01 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.01Hg0.99Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.01Hg0.99Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.01In0.99Te0.01As0.99\\\\n',\\n\",\n       \"  'output': ' No, Cd0.01In0.99Te0.01As0.99 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd0.02In0.98Te0.02As0.98\\\\n',\\n\",\n       \"  'output': ' No, Cd0.02In0.98Te0.02As0.98 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.03In0.97Te0.03As0.97\\\\n',\\n\",\n       \"  'output': ' No, Cd0.03In0.97Te0.03As0.97 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.04In0.96Te0.04As0.96\\\\n',\\n\",\n       \"  'output': ' No, Cd0.04In0.96Te0.04As0.96 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.05Ga0.95Sb0.95Te0.05\\\\n',\\n\",\n       \"  'output': ' No, Cd0.05Ga0.95Sb0.95Te0.05 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.05In0.95Te0.05As0.95\\\\n',\\n\",\n       \"  'output': ' No, Cd0.05In0.95Te0.05As0.95 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd0.06In0.94Te0.06As0.94\\\\n',\\n\",\n       \"  'output': ' No, Cd0.06In0.94Te0.06As0.94 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.07In0.93Te0.07As0.93\\\\n',\\n\",\n       \"  'output': ' No, Cd0.07In0.93Te0.07As0.93 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.1Ga0.9Sb0.9Te0.1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.1Ga0.9Sb0.9Te0.1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.1Hg0.9Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.1Hg0.9Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd0.1In0.9Te0.1As0.9\\\\n',\\n\",\n       \"  'output': ' No, Cd0.1In0.9Te0.1As0.9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.204Hg0.796Te1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.204Hg0.796Te1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.23Hg0.77Te1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.23Hg0.77Te1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.28Hg0.72Te1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.28Hg0.72Te1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.2Ga0.8Sb0.8Te0.2\\\\n',\\n\",\n       \"  'output': ' No, Cd0.2Ga0.8Sb0.8Te0.2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.2Hg0.8Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.2Hg0.8Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.2In2.4Ag0.4Te4\\\\n',\\n\",\n       \"  'output': ' No, Cd0.2In2.4Ag0.4Te4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.35Hg0.65Te1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.35Hg0.65Te1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.37Hg0.63Te1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.37Hg0.63Te1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd0.3Hg0.7Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.3Hg0.7Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.3Hg0.7Te1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.3Hg0.7Te1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd0.4Hg0.6Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.4Hg0.6Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.5Hg0.5Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.5Hg0.5Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.5In2.25Ag0.25Te4\\\\n',\\n\",\n       \"  'output': ' No, Cd0.5In2.25Ag0.25Te4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.5In2.2Ag0.4Te4\\\\n',\\n\",\n       \"  'output': ' No, Cd0.5In2.2Ag0.4Te4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd0.6Hg0.4Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.6Hg0.4Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.75In2.1Ag0.2Te4\\\\n',\\n\",\n       \"  'output': ' No, Cd0.75In2.1Ag0.2Te4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.7Hg0.3Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.7Hg0.3Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.8Hg0.2Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.8Hg0.2Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.8In2.1Ag0.1Te4\\\\n',\\n\",\n       \"  'output': ' No, Cd0.8In2.1Ag0.1Te4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.99Ga0.01Sb0.01Te0.99\\\\n',\\n\",\n       \"  'output': ' No, Cd0.99Ga0.01Sb0.01Te0.99 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.99Hg0.01Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.99Hg0.01Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd0.9Hg0.1Se1\\\\n',\\n\",\n       \"  'output': ' No, Cd0.9Hg0.1Se1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd12Ge17(B4O29)2\\\\n',\\n\",\n       \"  'output': ' No, Cd12Ge17(B4O29)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd13I28\\\\n',\\n\",\n       \"  'output': ' Yes, Cd13I28 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd1Hg6.5As4Cl6\\\\n',\\n\",\n       \"  'output': ' No, Cd1Hg6.5As4Cl6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd1Se0.01S0.99\\\\n',\\n\",\n       \"  'output': ' No, Cd1Se0.01S0.99 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd1Se0.2S0.8\\\\n',\\n\",\n       \"  'output': ' No, Cd1Se0.2S0.8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd1Se0.35S0.65\\\\n',\\n\",\n       \"  'output': ' No, Cd1Se0.35S0.65 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd1Se0.45S0.55\\\\n',\\n\",\n       \"  'output': ' No, Cd1Se0.45S0.55 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd1Se0.65S0.35\\\\n',\\n\",\n       \"  'output': ' No, Cd1Se0.65S0.35 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd1Se0.99S0.01\\\\n',\\n\",\n       \"  'output': ' No, Cd1Se0.99S0.01 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd2AgRh\\\\n',\\n\",\n       \"  'output': ' Yes, Cd2AgRh is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd2InAgTe3\\\\n',\\n\",\n       \"  'output': ' No, Cd2InAgTe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd2InCuTe3\\\\n',\\n\",\n       \"  'output': ' No, Cd2InCuTe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd2InCuTe4\\\\n',\\n\",\n       \"  'output': ' No, Cd2InCuTe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd2PbO4\\\\n',\\n\",\n       \"  'output': ' Yes, Cd2PbO4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd3AgPS6\\\\n',\\n\",\n       \"  'output': ' No, Cd3AgPS6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd3As2\\\\n',\\n\",\n       \"  'output': ' No, Cd3As2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd3Bi(PO4)3\\\\n',\\n\",\n       \"  'output': ' No, Cd3Bi(PO4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd3Bi2\\\\n',\\n\",\n       \"  'output': ' No, Cd3Bi2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd3In2(Te2S)2\\\\n',\\n\",\n       \"  'output': ' No, Cd3In2(Te2S)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd3P2\\\\n',\\n\",\n       \"  'output': ' No, Cd3P2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd3Sb2\\\\n',\\n\",\n       \"  'output': ' No, Cd3Sb2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd3Te2MoO10\\\\n',\\n\",\n       \"  'output': ' No, Cd3Te2MoO10 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd4As2Br3\\\\n',\\n\",\n       \"  'output': ' No, Cd4As2Br3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd4As2I3\\\\n',\\n\",\n       \"  'output': ' No, Cd4As2I3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd4P2Br3\\\\n',\\n\",\n       \"  'output': ' No, Cd4P2Br3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd4P2Cl3\\\\n',\\n\",\n       \"  'output': ' No, Cd4P2Cl3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd4P2I3\\\\n',\\n\",\n       \"  'output': ' No, Cd4P2I3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd4Sb2I3\\\\n',\\n\",\n       \"  'output': ' No, Cd4Sb2I3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cd4Sb3\\\\n',\\n\",\n       \"  'output': ' No, Cd4Sb3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cd5Ga2(Te3S)2\\\\n',\\n\",\n       \"  'output': ' No, Cd5Ga2(Te3S)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd6P7\\\\n',\\n\",\n       \"  'output': ' No, Cd6P7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cd8B5O15F\\\\n',\\n\",\n       \"  'output': ' No, Cd8B5O15F is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdAg\\\\n',\\n\",\n       \"  'output': ' Yes, CdAg is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdAg2(PS3)2\\\\n',\\n\",\n       \"  'output': ' No, CdAg2(PS3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdAg2GeS4\\\\n',\\n\",\n       \"  'output': ' No, CdAg2GeS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdAs2\\\\n',\\n\",\n       \"  'output': ' No, CdAs2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdAsPd5\\\\n',\\n\",\n       \"  'output': ' Yes, CdAsPd5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdAuO2\\\\n',\\n\",\n       \"  'output': ' Yes, CdAuO2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdBiClO2\\\\n',\\n\",\n       \"  'output': ' No, CdBiClO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdBr2\\\\n',\\n\",\n       \"  'output': ' No, CdBr2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdCl2\\\\n',\\n\",\n       \"  'output': ' No, CdCl2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdCu(SeO3)2\\\\n',\\n\",\n       \"  'output': ' No, CdCu(SeO3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdCu2GeS4\\\\n',\\n\",\n       \"  'output': ' No, CdCu2GeS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdCu2GeSe4\\\\n',\\n\",\n       \"  'output': ' No, CdCu2GeSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdCu2SnS4\\\\n',\\n\",\n       \"  'output': ' No, CdCu2SnS4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdCu2SnSe4\\\\n',\\n\",\n       \"  'output': ' No, CdCu2SnSe4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdF2\\\\n',\\n\",\n       \"  'output': ' No, CdF2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdGeAs2\\\\n',\\n\",\n       \"  'output': ' No, CdGeAs2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdGeP2\\\\n',\\n\",\n       \"  'output': ' No, CdGeP2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdHIO4\\\\n',\\n\",\n       \"  'output': ' No, CdHIO4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdHg4(AsI2)2\\\\n',\\n\",\n       \"  'output': ' No, CdHg4(AsI2)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdHg6(As2Br3)2\\\\n',\\n\",\n       \"  'output': ' No, CdHg6(As2Br3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdI2\\\\n',\\n\",\n       \"  'output': ' No, CdI2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdIClO3\\\\n',\\n\",\n       \"  'output': ' No, CdIClO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdIn\\\\n',\\n\",\n       \"  'output': ' No, CdIn is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdIn8Te13\\\\n',\\n\",\n       \"  'output': ' No, CdIn8Te13 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdInCuSe3\\\\n',\\n\",\n       \"  'output': ' No, CdInCuSe3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdO\\\\n',\\n\",\n       \"  'output': ' No, CdO is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdP2\\\\n',\\n\",\n       \"  'output': ' No, CdP2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdP4\\\\n',\\n\",\n       \"  'output': ' No, CdP4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdP4PbO12\\\\n',\\n\",\n       \"  'output': ' No, CdP4PbO12 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdPd\\\\n',\\n\",\n       \"  'output': ' Yes, CdPd is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdPt\\\\n',\\n\",\n       \"  'output': ' Yes, CdPt is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdRhF6\\\\n',\\n\",\n       \"  'output': ' Yes, CdRhF6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdS\\\\n',\\n\",\n       \"  'output': ' No, CdS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdSb\\\\n',\\n\",\n       \"  'output': ' No, CdSb is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdSb2Se3Br2\\\\n',\\n\",\n       \"  'output': ' No, CdSb2Se3Br2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdSb4MoO10\\\\n',\\n\",\n       \"  'output': ' No, CdSb4MoO10 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdSe\\\\n',\\n\",\n       \"  'output': ' No, CdSe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdSiAs2\\\\n',\\n\",\n       \"  'output': ' No, CdSiAs2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdSiP2\\\\n',\\n\",\n       \"  'output': ' No, CdSiP2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdSnAs2\\\\n',\\n\",\n       \"  'output': ' No, CdSnAs2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CdSnO3\\\\n',\\n\",\n       \"  'output': ' No, CdSnO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CdSnP2\\\\n',\\n\",\n       \"  'output': ' No, CdSnP2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdTe\\\\n',\\n\",\n       \"  'output': ' No, CdTe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CdTeO3\\\\n',\\n\",\n       \"  'output': ' No, CdTeO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce(AlZn)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(AlZn)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce(BC)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(BC)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce(CoAs)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(CoAs)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce(CoB)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(CoB)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce(CuSb)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(CuSb)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce(HO)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(HO)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce(InS2)3\\\\n',\\n\",\n       \"  'output': ' No, Ce(InS2)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce(MnGe)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(MnGe)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce(MnSi)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(MnSi)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce(PPt2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(PPt2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce(SiAu)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(SiAu)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce(SiNi)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(SiNi)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce(SiPd)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce(SiPd)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce1.3Lu0.7S3\\\\n',\\n\",\n       \"  'output': ' No, Ce1.3Lu0.7S3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce10Se14O\\\\n',\\n\",\n       \"  'output': ' No, Ce10Se14O is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce15B8N25\\\\n',\\n\",\n       \"  'output': ' No, Ce15B8N25 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce1Mn0.5Se1O1\\\\n',\\n\",\n       \"  'output': ' No, Ce1Mn0.5Se1O1 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2(SbPd3)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2(SbPd3)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2(SnSe3)3\\\\n',\\n\",\n       \"  'output': ' No, Ce2(SnSe3)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2Al2Co15\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2Al2Co15 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2Co5B2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2Co5B2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2CrN3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2CrN3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2Cu(NO)2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2Cu(NO)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2Fe(SeO)2\\\\n',\\n\",\n       \"  'output': ' No, Ce2Fe(SeO)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2Fe17\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2Fe17 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2Ge2Se7\\\\n',\\n\",\n       \"  'output': ' No, Ce2Ge2Se7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2GeSe5\\\\n',\\n\",\n       \"  'output': ' No, Ce2GeSe5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2S2O\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2S2O is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2S3\\\\n',\\n\",\n       \"  'output': ' No, Ce2S3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2Sb\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2Sb is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2Se3\\\\n',\\n\",\n       \"  'output': ' No, Ce2Se3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce2SiSeO4\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2SiSeO4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce2Te3\\\\n',\\n\",\n       \"  'output': ' No, Ce2Te3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce2Ti2O7\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2Ti2O7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce2ZnNi2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce2ZnNi2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce3(Al3Ru)4\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3(Al3Ru)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce3Al\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3Al is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce3AlC\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3AlC is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce3B2(ClO2)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3B2(ClO2)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce3In3Ru2\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3In3Ru2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce3LuSe6\\\\n',\\n\",\n       \"  'output': ' No, Ce3LuSe6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce3MnAlS7\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3MnAlS7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce3MoO7\\\\n',\\n\",\n       \"  'output': ' No, Ce3MoO7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce3NbS3O4\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3NbS3O4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce3Pd5\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3Pd5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce3SiPt5\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3SiPt5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce3Ta(ClO2)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3Ta(ClO2)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce3TaO7\\\\n',\\n\",\n       \"  'output': ' Yes, Ce3TaO7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce4(GeS4)3\\\\n',\\n\",\n       \"  'output': ' No, Ce4(GeS4)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce4Bi3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce4Bi3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce4FeSe6O\\\\n',\\n\",\n       \"  'output': ' Yes, Ce4FeSe6O is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce4InSbSe9\\\\n',\\n\",\n       \"  'output': ' No, Ce4InSbSe9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce4Si3Rh4\\\\n',\\n\",\n       \"  'output': ' Yes, Ce4Si3Rh4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce4Te7\\\\n',\\n\",\n       \"  'output': ' No, Ce4Te7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce5(SiN3)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce5(SiN3)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Ce5CuSe8\\\\n',\\n\",\n       \"  'output': ' Yes, Ce5CuSe8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce5Ge3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce5Ge3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce5Si3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce5Si3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce6B2(CBr)3\\\\n',\\n\",\n       \"  'output': ' Yes, Ce6B2(CBr)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce8Sb2S15\\\\n',\\n\",\n       \"  'output': ' No, Ce8Sb2S15 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Ce8U2O21\\\\n',\\n\",\n       \"  'output': ' Yes, Ce8U2O21 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Ce9SmO20\\\\n',\\n\",\n       \"  'output': ' Yes, Ce9SmO20 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeAgSn\\\\n',\\n\",\n       \"  'output': ' Yes, CeAgSn is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeAl2Pd5\\\\n',\\n\",\n       \"  'output': ' Yes, CeAl2Pd5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeAl2Pt3\\\\n',\\n\",\n       \"  'output': ' Yes, CeAl2Pt3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeAl3Ni2\\\\n',\\n\",\n       \"  'output': ' Yes, CeAl3Ni2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeAlO3\\\\n',\\n\",\n       \"  'output': ' Yes, CeAlO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeAlSi2\\\\n',\\n\",\n       \"  'output': ' Yes, CeAlSi2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeAsPd\\\\n',\\n\",\n       \"  'output': ' Yes, CeAsPd is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeAsSe\\\\n',\\n\",\n       \"  'output': ' Yes, CeAsSe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeB2Ir3\\\\n',\\n\",\n       \"  'output': ' Yes, CeB2Ir3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeBC\\\\n',\\n\",\n       \"  'output': ' Yes, CeBC is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeBiW2O9\\\\n',\\n\",\n       \"  'output': ' No, CeBiW2O9 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeCd2Ag\\\\n',\\n\",\n       \"  'output': ' Yes, CeCd2Ag is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeCdAu2\\\\n',\\n\",\n       \"  'output': ' Yes, CeCdAu2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeCoGeH\\\\n',\\n\",\n       \"  'output': ' Yes, CeCoGeH is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeF3\\\\n',\\n\",\n       \"  'output': ' No, CeF3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeGaO3\\\\n',\\n\",\n       \"  'output': ' Yes, CeGaO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeHSe\\\\n',\\n\",\n       \"  'output': ' Yes, CeHSe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeHg\\\\n',\\n\",\n       \"  'output': ' Yes, CeHg is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeInIr\\\\n',\\n\",\n       \"  'output': ' Yes, CeInIr is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeIr5\\\\n',\\n\",\n       \"  'output': ' Yes, CeIr5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeLu3\\\\n',\\n\",\n       \"  'output': ' Yes, CeLu3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeMg2Ag\\\\n',\\n\",\n       \"  'output': ' Yes, CeMg2Ag is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeMgAg2\\\\n',\\n\",\n       \"  'output': ' Yes, CeMgAg2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeMgNi4\\\\n',\\n\",\n       \"  'output': ' Yes, CeMgNi4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeMgPt\\\\n',\\n\",\n       \"  'output': ' Yes, CeMgPt is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeMgZn2\\\\n',\\n\",\n       \"  'output': ' Yes, CeMgZn2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeMoO4F\\\\n',\\n\",\n       \"  'output': ' No, CeMoO4F is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeN\\\\n',\\n\",\n       \"  'output': ' No, CeN is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeNbO4\\\\n',\\n\",\n       \"  'output': ' Yes, CeNbO4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeO2\\\\n',\\n\",\n       \"  'output': ' No, CeO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeOs2\\\\n',\\n\",\n       \"  'output': ' Yes, CeOs2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CePd5\\\\n',\\n\",\n       \"  'output': ' Yes, CePd5 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CePrO2\\\\n',\\n\",\n       \"  'output': ' Yes, CePrO2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeRh\\\\n',\\n\",\n       \"  'output': ' Yes, CeRh is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeSI\\\\n',\\n\",\n       \"  'output': ' Yes, CeSI is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeSbO3\\\\n',\\n\",\n       \"  'output': ' Yes, CeSbO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeScO3\\\\n',\\n\",\n       \"  'output': ' No, CeScO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeSi2Ni\\\\n',\\n\",\n       \"  'output': ' Yes, CeSi2Ni is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeSi2Pt\\\\n',\\n\",\n       \"  'output': ' Yes, CeSi2Pt is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeSiI\\\\n',\\n\",\n       \"  'output': ' Yes, CeSiI is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CeSiIr\\\\n',\\n\",\n       \"  'output': ' Yes, CeSiIr is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeSiOs\\\\n',\\n\",\n       \"  'output': ' Yes, CeSiOs is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeTaN2O\\\\n',\\n\",\n       \"  'output': ' No, CeTaN2O is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeTl2P2S7\\\\n',\\n\",\n       \"  'output': ' No, CeTl2P2S7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeTl3\\\\n',\\n\",\n       \"  'output': ' Yes, CeTl3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CeTlZn\\\\n',\\n\",\n       \"  'output': ' Yes, CeTlZn is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CeZnPO\\\\n',\\n\",\n       \"  'output': ' Yes, CeZnPO is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Co(PO3)4\\\\n',\\n\",\n       \"  'output': ' Yes, Co(PO3)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Co(WO4)2\\\\n',\\n\",\n       \"  'output': ' Yes, Co(WO4)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Co1Te1.88\\\\n',\\n\",\n       \"  'output': ' No, Co1Te1.88 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Co2B4Mo\\\\n',\\n\",\n       \"  'output': ' Yes, Co2B4Mo is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Co2Ge\\\\n',\\n\",\n       \"  'output': ' Yes, Co2Ge is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Co2O3\\\\n',\\n\",\n       \"  'output': ' Yes, Co2O3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Co2Te3O8\\\\n',\\n\",\n       \"  'output': ' No, Co2Te3O8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Co3H\\\\n',\\n\",\n       \"  'output': ' Yes, Co3H is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Co3Se4\\\\n',\\n\",\n       \"  'output': ' Yes, Co3Se4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Co3W\\\\n',\\n\",\n       \"  'output': ' Yes, Co3W is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Co5Ge7\\\\n',\\n\",\n       \"  'output': ' Yes, Co5Ge7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Co5RuO8\\\\n',\\n\",\n       \"  'output': ' Yes, Co5RuO8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Co7Mo6\\\\n',\\n\",\n       \"  'output': ' Yes, Co7Mo6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Co7Re17O48\\\\n',\\n\",\n       \"  'output': ' Yes, Co7Re17O48 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CoAs3\\\\n',\\n\",\n       \"  'output': ' No, CoAs3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CoAsRh\\\\n',\\n\",\n       \"  'output': ' Yes, CoAsRh is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CoAsS\\\\n',\\n\",\n       \"  'output': ' No, CoAsS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CoAsSe\\\\n',\\n\",\n       \"  'output': ' No, CoAsSe is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CoCu2Sn\\\\n',\\n\",\n       \"  'output': ' Yes, CoCu2Sn is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CoGe\\\\n',\\n\",\n       \"  'output': ' Yes, CoGe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CoH2(SN)4\\\\n',\\n\",\n       \"  'output': ' Yes, CoH2(SN)4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CoMoP2\\\\n',\\n\",\n       \"  'output': ' Yes, CoMoP2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CoN\\\\n',\\n\",\n       \"  'output': ' Yes, CoN is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CoOF\\\\n',\\n\",\n       \"  'output': ' Yes, CoOF is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CoP2\\\\n',\\n\",\n       \"  'output': ' No, CoP2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CoP3\\\\n',\\n\",\n       \"  'output': ' No, CoP3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CoPS\\\\n',\\n\",\n       \"  'output': ' No, CoPS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CoPbO3\\\\n',\\n\",\n       \"  'output': ' Yes, CoPbO3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CoSb2\\\\n',\\n\",\n       \"  'output': ' No, CoSb2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CoSb3\\\\n',\\n\",\n       \"  'output': ' No, CoSb3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CoSbS\\\\n',\\n\",\n       \"  'output': ' No, CoSbS is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr(FeSe2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Cr(FeSe2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cr(MoS2)2\\\\n',\\n\",\n       \"  'output': ' Yes, Cr(MoS2)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cr10Sb3Te7\\\\n',\\n\",\n       \"  'output': ' Yes, Cr10Sb3Te7 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cr2CuS4\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2CuS4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr2CuTe4\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2CuTe4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr2GeC\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2GeC is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr2HO4\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2HO4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cr2HgSe4\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2HgSe4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cr2NiS4\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2NiS4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr2O3\\\\n',\\n\",\n       \"  'output': ' No, Cr2O3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cr2P3O11\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2P3O11 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr2S3\\\\n',\\n\",\n       \"  'output': ' No, Cr2S3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cr2SbTe\\\\n',\\n\",\n       \"  'output': ' Yes, Cr2SbTe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cr3N2\\\\n',\\n\",\n       \"  'output': ' Yes, Cr3N2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr3Ni(PO4)6\\\\n',\\n\",\n       \"  'output': ' Yes, Cr3Ni(PO4)6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr3P\\\\n',\\n\",\n       \"  'output': ' Yes, Cr3P is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr3Se4\\\\n',\\n\",\n       \"  'output': ' No, Cr3Se4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cr4As3\\\\n',\\n\",\n       \"  'output': ' Yes, Cr4As3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cr4Cu3Te8\\\\n',\\n\",\n       \"  'output': ' Yes, Cr4Cu3Te8 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cr7C3\\\\n',\\n\",\n       \"  'output': ' Yes, Cr7C3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrAs\\\\n',\\n\",\n       \"  'output': ' Yes, CrAs is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CrB2(PbO2)6\\\\n',\\n\",\n       \"  'output': ' No, CrB2(PbO2)6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CrBi2I2O11\\\\n',\\n\",\n       \"  'output': ' No, CrBi2I2O11 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CrCo2Bi\\\\n',\\n\",\n       \"  'output': ' Yes, CrCo2Bi is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrCoGe\\\\n',\\n\",\n       \"  'output': ' Yes, CrCoGe is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrCoPt2\\\\n',\\n\",\n       \"  'output': ' Yes, CrCoPt2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrCu2Si\\\\n',\\n\",\n       \"  'output': ' Yes, CrCu2Si is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CrFe2Sb\\\\n',\\n\",\n       \"  'output': ' Yes, CrFe2Sb is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrFeP\\\\n',\\n\",\n       \"  'output': ' Yes, CrFeP is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrH9(CN2)3\\\\n',\\n\",\n       \"  'output': ' Yes, CrH9(CN2)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CrIrO4\\\\n',\\n\",\n       \"  'output': ' Yes, CrIrO4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrIrO6\\\\n',\\n\",\n       \"  'output': ' Yes, CrIrO6 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CrNi3\\\\n',\\n\",\n       \"  'output': ' Yes, CrNi3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrNiAs\\\\n',\\n\",\n       \"  'output': ' Yes, CrNiAs is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CrNiP2O9\\\\n',\\n\",\n       \"  'output': ' Yes, CrNiP2O9 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CrO2\\\\n',\\n\",\n       \"  'output': ' No, CrO2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' CrO3\\\\n',\\n\",\n       \"  'output': ' No, CrO3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CrPbO4\\\\n',\\n\",\n       \"  'output': ' No, CrPbO4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' CrSb2\\\\n',\\n\",\n       \"  'output': ' No, CrSb2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CrSi2\\\\n',\\n\",\n       \"  'output': ' No, CrSi2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' CrTe2\\\\n',\\n\",\n       \"  'output': ' No, CrTe2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cs(AsRu)2\\\\n',\\n\",\n       \"  'output': ' Yes, Cs(AsRu)2 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs(MoO3)3\\\\n',\\n\",\n       \"  'output': ' Yes, Cs(MoO3)3 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs0.4K0.6P1Se6\\\\n',\\n\",\n       \"  'output': ' No, Cs0.4K0.6P1Se6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs1.13Cd1.13Bi2.87Se6\\\\n',\\n\",\n       \"  'output': ' No, Cs1.13Cd1.13Bi2.87Se6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs1.43Cd1.43Bi2.57S6\\\\n',\\n\",\n       \"  'output': ' No, Cs1.43Cd1.43Bi2.57S6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs10Cd4Sn4S17\\\\n',\\n\",\n       \"  'output': ' No, Cs10Cd4Sn4S17 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs2AgBiBr6\\\\n',\\n\",\n       \"  'output': ' No, Cs2AgBiBr6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2AgBiCl6\\\\n',\\n\",\n       \"  'output': ' No, Cs2AgBiCl6 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Al2B2O7\\\\n',\\n\",\n       \"  'output': ' No, Cs2Al2B2O7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Ba3(P2O7)2\\\\n',\\n\",\n       \"  'output': ' No, Cs2Ba3(P2O7)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Cd(PSe3)2\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cd(PSe3)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Cd0.25Hg5.75S7\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cd0.25Hg5.75S7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Cd1.35Hg4.65S7\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cd1.35Hg4.65S7 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cs2Cd2Bi2S5\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cd2Bi2S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Cd3(B4O7)4\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cd3(B4O7)4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Cd3Te4\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cd3Te4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs2CrCl4\\\\n',\\n\",\n       \"  'output': ' Yes, Cs2CrCl4 is metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Cu(PS3)3\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cu(PS3)3 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs2Cu2Sb2S5\\\\n',\\n\",\n       \"  'output': ' No, Cs2Cu2Sb2S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs2DyCu3Te4\\\\n',\\n\",\n       \"  'output': ' No, Cs2DyCu3Te4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs2Ga2S5\\\\n',\\n\",\n       \"  'output': ' No, Cs2Ga2S5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Ga2Se5\\\\n',\\n\",\n       \"  'output': ' No, Cs2Ga2Se5 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is composition metal? ->',\\n\",\n       \"  'input': ' Cs2Hg(ICl)2\\\\n',\\n\",\n       \"  'output': ' No, Cs2Hg(ICl)2 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Hg3I8\\\\n',\\n\",\n       \"  'output': ' No, Cs2Hg3I8 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Is given composition metal? ->',\\n\",\n       \"  'input': ' Cs2Hg3S4\\\\n',\\n\",\n       \"  'output': ' No, Cs2Hg3S4 is not metal.\\\\n'},\\n\",\n       \" {'instruction': 'Given composition, is it metal? ->',\\n\",\n       \"  'input': ' Cs2Hg6S7\\\\n',\\n\",\n       \"  'output': ' No, Cs2Hg6S7 is not metal.\\\\n'},\\n\",\n       \" ...]\"\n      ]\n     },\n     \"execution_count\": 2,\n     \"metadata\": {},\n     \"output_type\": \"execute_result\"\n    }\n   ],\n   \"source\": [\n    \"data_list\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 3,\n   \"id\": \"166b1e11\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 4,\n   \"id\": \"52c48afe\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"4921\\n\",\n      \"164\\n\",\n      \"['year', 'helicopter', 'direction', 'market', 'legal', 'skill', 'ash', 'mascara', 'lier', 'fold']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"print(len(data_list))\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add = int(len(data_list)/30)\\n\",\n    \"print(add)\\n\",\n    \"add_nouns = random.sample(nouns, add)\\n\",\n    \"print(add_nouns[:10])\\n\",\n    \"for an in add_nouns:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    ran2 = random.sample(list(slot.values()), 1)[0]\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"Is composition metal? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Is given composition metal? ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given composition, is it metal? ->\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] = \\\" \\\" + an + \\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" \\\"+an+\\\" is not a \\\"+ran2+\\\" and it is not metal.\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\\n\",\n    \"random.shuffle(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"e77195f1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.8.0\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/matbench_is_metal/matbench_is_metal.csv",
    "content": "composition,is metal?\nAg(AuS)2,TRUE\nAg(W3Br7)2,TRUE\nAg0.5Ge1Pb1.75S4,FALSE\nAg0.5Ge1Pb1.75Se4,FALSE\nAg2BBr,TRUE\nAg2BiO3,TRUE\nAg2GeS3,FALSE\nAg2GeSe3,FALSE\nAg2GeTe3,FALSE\nAg2HgI4,FALSE\nAg2Mo(I2O7)2,FALSE\nAg2O,FALSE\nAg2P2PbO7,TRUE\nAg2PdO2,FALSE\nAg2S,FALSE\nAg2SnS3,FALSE\nAg2SnSe3,FALSE\nAg3AsO4,TRUE\nAg3AsS3,FALSE\nAg3AsSe3,FALSE\nAg3Pd,TRUE\nAg3RuO4,TRUE\nAg3SbS3,FALSE\nAg5IO6,FALSE\nAg7(SI)2,TRUE\nAg7AsS6,FALSE\nAg7AsSe6,FALSE\nAg7NO11,TRUE\nAg8GeS6,FALSE\nAg8SnSe6,FALSE\nAg9(PbO3)4,TRUE\nAg9Ge2IO8,TRUE\nAgAsS2,FALSE\nAgAsSe2,FALSE\nAgAu3,TRUE\nAgBi(PS3)2,FALSE\nAgBi(PSe3)2,FALSE\nAgBiPbS3,FALSE\nAgBiPbSe3,FALSE\nAgBiS2,FALSE\nAgBiSe2,FALSE\nAgBr,FALSE\nAgCNO,TRUE\nAgCl,FALSE\nAgF,FALSE\nAgGeO3,TRUE\nAgI,FALSE\nAgN3,FALSE\nAgO,FALSE\nAgP15,FALSE\nAgPd(IO3)3,FALSE\nAgPdO2,TRUE\nAgPt3,TRUE\nAgS,FALSE\nAgSO4,FALSE\nAgSbS2,FALSE\nAgSbSe2,FALSE\nAgSbTe2,FALSE\nAgTe,FALSE\nAgTe2As,FALSE\nAl(Ni10B7)2,TRUE\nAl(NiS2)2,TRUE\nAl0.01Cd0.99Sb0.01Te0.99,FALSE\nAl0.01Ga0.99P1,FALSE\nAl0.01In0.99P1,FALSE\nAl0.05Cd0.95Sb0.05Te0.95,FALSE\nAl0.15Ga0.85As1,FALSE\nAl0.1Cd0.9Sb0.1Te0.9,FALSE\nAl0.1In0.9P1,FALSE\nAl0.2Ga0.8P1,FALSE\nAl0.2In0.8P1,FALSE\nAl0.35Ga0.65As1,FALSE\nAl0.3Ga0.7As1,FALSE\nAl0.3In0.7P1,FALSE\nAl0.45Cd0.55Sb0.45Te0.55,FALSE\nAl0.4Cd0.6Sb0.4Te0.6,FALSE\nAl0.4Ga0.6P1,FALSE\nAl0.4In0.6P1,FALSE\nAl0.5Ga0.5As1,FALSE\nAl0.5In0.5P1,FALSE\nAl0.6Ga0.4As1,FALSE\nAl0.6Ga0.4P1,FALSE\nAl0.6In0.4P1,FALSE\nAl0.75Ga0.25As1,FALSE\nAl0.7In0.3P1,FALSE\nAl0.8Ga0.2P1,FALSE\nAl0.99Cd0.01Sb0.99Te0.01,FALSE\nAl0.99Ga0.01P1,FALSE\nAl0.99In0.01P1,FALSE\nAl10V,TRUE\nAl13Ru4,TRUE\nAl2(CuSe2)3,TRUE\nAl21Pt8,TRUE\nAl2CoIr,TRUE\nAl2Cr2O7,TRUE\nAl2CrS4,TRUE\nAl2Cu,TRUE\nAl2FeNi,TRUE\nAl2Ru,TRUE\nAl2S3,FALSE\nAl2Se3,FALSE\nAl2Te3,FALSE\nAl3Tc,TRUE\nAl4Cu2O7,TRUE\nAl4Cu9,TRUE\nAl5Rh2,TRUE\nAl6Fe,TRUE\nAl6Ru,TRUE\nAl6Tc,TRUE\nAl7(CN)3,TRUE\nAl9Co2,TRUE\nAl9Ir2,TRUE\nAl9Rh2,TRUE\nAlAgO2,FALSE\nAlAgS2,FALSE\nAlAgSe2,FALSE\nAlAgTe2,FALSE\nAlAs,TRUE\nAlB12,FALSE\nAlB2,TRUE\nAlBi,FALSE\nAlCoO3,TRUE\nAlCu3,TRUE\nAlCu7O12,TRUE\nAlCuS2,FALSE\nAlCuSe2,FALSE\nAlCuTe2,FALSE\nAlFe2Si,TRUE\nAlFe4(CuO4)3,TRUE\nAlIr,TRUE\nAlN,FALSE\nAlNi2,TRUE\nAlP,FALSE\nAlPd5I2,TRUE\nAlSb,FALSE\nAlSn,TRUE\nAlV(TeO4)2,FALSE\nAlVCo2,TRUE\nAs2Ir,FALSE\nAs2O3,FALSE\nAs2Os,FALSE\nAs2Pt,FALSE\nAs2Rh,FALSE\nAs2Ru,FALSE\nAs2S3,FALSE\nAs2S5,FALSE\nAs2Se3,FALSE\nAsAu3,TRUE\nAsBr3,FALSE\nAsI3,FALSE\nAsOsS,FALSE\nAsP,FALSE\nAsPPd,FALSE\nAsPPt,FALSE\nAsPRu,FALSE\nAsPd3Pb2,TRUE\nAsRuS,FALSE\nAsS,FALSE\nAsS3,FALSE\nAsSI,FALSE\nAsSeBr,TRUE\nAsSeI,FALSE\nAu3S,TRUE\nAuBrO2,TRUE\nB2Mo(PbO2)6,FALSE\nB2O3,FALSE\nB2Se2O7,FALSE\nB3H2Pb2O7.5,FALSE\nB3Pb10Br3O13,FALSE\nB3Pb3NO10,FALSE\nB4C,FALSE\nB4H2Pb6O13,FALSE\nB4W,TRUE\nB5Mo2,TRUE\nB6As,FALSE\nB6P,FALSE\nBAs,FALSE\nBH(PbO2)2,FALSE\nBMo,TRUE\nBP,FALSE\nBPb2ClO3,FALSE\nBPb6BrO7,FALSE\nBPb7Br3O7,FALSE\nBRh2,TRUE\nBSb,FALSE\nBSbPbS4,FALSE\nBSe2Cl,TRUE\nBTe2As,TRUE\nBa(AsPd)2,TRUE\nBa(AsRh)2,TRUE\nBa(BO2)2,FALSE\nBa(BRh)2,TRUE\nBa(FeS2)2,TRUE\nBa(GaS2)2,FALSE\nBa(GaSe2)2,FALSE\nBa(InS2)2,FALSE\nBa(InSe2)2,FALSE\nBa(NiP2)2,TRUE\nBa(PdO2)2,TRUE\nBa(SnO2)4,TRUE\nBa(ZnAs)2,FALSE\nBa1.88Ta15O32,FALSE\nBa12In4S19,FALSE\nBa14Ir8(PdO11)3,TRUE\nBa14Na8CaN6,TRUE\nBa23Ga8(SbS19)2,FALSE\nBa2B4H2O9,FALSE\nBa2B6H4O13,FALSE\nBa2B6O11,FALSE\nBa2BiSbO6,TRUE\nBa2CaOsO6,TRUE\nBa2CaReO6,TRUE\nBa2Cd(BO2)6,FALSE\nBa2Ce2O5,TRUE\nBa2CeInTe5,FALSE\nBa2CoWO6,TRUE\nBa2Cu5F14,TRUE\nBa2CuWO6,TRUE\nBa2DyCu3O7,TRUE\nBa2DyGaSe5,FALSE\nBa2DyGaTe5,FALSE\nBa2DyInSe5,FALSE\nBa2DyInTe5,FALSE\nBa2ErGaSe5,FALSE\nBa2ErGaTe5,FALSE\nBa2ErInSe5,FALSE\nBa2ErInTe5,FALSE\nBa2FeMoO6,TRUE\nBa2FeReO6,TRUE\nBa2Ga8GeS16,FALSE\nBa2Ga8SiS16,FALSE\nBa2GaAsSe5,FALSE\nBa2GaBiS5,FALSE\nBa2GaBiSe5,FALSE\nBa2GaBiTe5,FALSE\nBa2GaS4,FALSE\nBa2GaSbSe5,FALSE\nBa2GaSbTe5,FALSE\nBa2GaSe4,FALSE\nBa2GdGaSe5,FALSE\nBa2GdGaTe5,FALSE\nBa2GdInSe5,FALSE\nBa2GdInTe5,FALSE\nBa2HgS5,FALSE\nBa2In2S5,FALSE\nBa2In2Se5,FALSE\nBa2InAgS4,FALSE\nBa2InBiS5,FALSE\nBa2InSbSe5,FALSE\nBa2LaIrO6,TRUE\nBa2LiFe2N3,TRUE\nBa2NaCu3S5,FALSE\nBa2NdGaS5,FALSE\nBa2NdGaSe5,FALSE\nBa2NdInSe5,FALSE\nBa2NdInTe5,FALSE\nBa2ReNiO6,TRUE\nBa2Sb7HO14,FALSE\nBa2ScIrO6,TRUE\nBa2ScTaO6,FALSE\nBa2SmCu3O7,TRUE\nBa2SmGaSe5,FALSE\nBa2SmGaTe5,FALSE\nBa2SmInSe5,FALSE\nBa2SmInTe5,FALSE\nBa2SmTaO6,FALSE\nBa2SnSe4,FALSE\nBa2SnSe5,FALSE\nBa2TaInO6,FALSE\nBa2TbIrO6,TRUE\nBa2ThCu2Se5,FALSE\nBa2UCuO6,TRUE\nBa2V2Te2O11,FALSE\nBa2V2ZnO8,FALSE\nBa2V4(TeO6)3,FALSE\nBa2YGaSe5,FALSE\nBa2YGaTe5,FALSE\nBa2YInSe5,FALSE\nBa2YInTe5,FALSE\nBa2YReO6,TRUE\nBa2Yb(CuO2)4,TRUE\nBa2Zn0.2B2S5.2,FALSE\nBa2ZnSe3,FALSE\nBa2ZnTe3,FALSE\nBa3(AlGe)2,TRUE\nBa3(LiSn2)4,TRUE\nBa3Ag2(SnS4)2,FALSE\nBa3B1.5Sb0.5S6,FALSE\nBa3BSbS6,FALSE\nBa3BSbSe6,FALSE\nBa3Bi0.5B1.5S6,FALSE\nBa3Bi2TeO9,FALSE\nBa3CaIr2O9,TRUE\nBa3CaRu2O9,TRUE\nBa3Cd(SnS4)2,FALSE\nBa3Co10O17,TRUE\nBa3CrS5,TRUE\nBa3Dy2(PS4)4,FALSE\nBa3Er2(PS4)4,FALSE\nBa3ErRu2O9,TRUE\nBa3Eu(PO4)3,FALSE\nBa3FeS4Br,FALSE\nBa3Gd2(PS4)4,FALSE\nBa3GeS5,FALSE\nBa3Ho2(PS4)4,FALSE\nBa3In2(PO4)4,FALSE\nBa3InS4Cl,FALSE\nBa3La3(Cu3O7)2,FALSE\nBa3MgTa2O9,FALSE\nBa3N2,TRUE\nBa3NaIr2O9,TRUE\nBa3NaIrO6,TRUE\nBa3Nb2CoO9,TRUE\nBa3Nb2Se9,FALSE\nBa3P3ClO10,FALSE\nBa3PN,TRUE\nBa3Sb2S7,FALSE\nBa3Sn(SbSe4)2,FALSE\nBa3Sn0.87Bi2.13Se8,FALSE\nBa3Ta2Se9,FALSE\nBa3Ta2ZnO9,FALSE\nBa3Ta5NO14,FALSE\nBa3Tb2(PS4)4,FALSE\nBa3Te,TRUE\nBa3ThSe7,FALSE\nBa3V2(SeO4)4,FALSE\nBa3YIr2O9,TRUE\nBa3Yb4O9,TRUE\nBa3ZrRu2O9,TRUE\nBa4B11O20F,FALSE\nBa4Ga4GeSe12,FALSE\nBa4Ga4SnSe12,FALSE\nBa4Ga5AgS12,FALSE\nBa4Ga5CuS12,FALSE\nBa4Ga5CuSe12,FALSE\nBa4Ga5Si18,FALSE\nBa4Ge3S9Cl2,FALSE\nBa4Ge3Se9Cl2,FALSE\nBa4InAgSe6,FALSE\nBa4InCuSe6,FALSE\nBa4LiGa5Se12,FALSE\nBa4Nb14O23,TRUE\nBa4Sb3S8Cl,FALSE\nBa4Si20Au3,TRUE\nBa4Si3Se9Cl2,FALSE\nBa4Sm2Cu2O9,TRUE\nBa4Yb(CuO3)3,TRUE\nBa5(Ga2Se5)2,FALSE\nBa5(GaSe4)2,FALSE\nBa5Al2Ge7,TRUE\nBa5Bi3,TRUE\nBa5Cd(Ga2Se5)3,FALSE\nBa5Ga6GeP12,FALSE\nBa5Ga6SnP12,FALSE\nBa5Ge3,TRUE\nBa5In4Bi5,TRUE\nBa5In4Te4S7,FALSE\nBa5Sb3,TRUE\nBa5V3O12F,FALSE\nBa6Ag2.7Sn4.3S16,FALSE\nBa6Al4B14O33,FALSE\nBa6Ga2SnSe11,FALSE\nBa6In2NF,TRUE\nBa6Sn6Se13,FALSE\nBa7(SnS3)5,FALSE\nBa7B3O9F5,FALSE\nBa7Ga5AgS15,FALSE\nBa7Ru4Br2O15,TRUE\nBa8Al10B12O41,FALSE\nBa8Hg4Se7S5,FALSE\nBa8Sn4S15,FALSE\nBa8Ta7O24,TRUE\nBaAg,TRUE\nBaAg2,TRUE\nBaAgSbS3,FALSE\nBaAl2,TRUE\nBaAl4Se7,FALSE\nBaAlCu4O7,TRUE\nBaAu(IO3)5,FALSE\nBaAu2,TRUE\nBaB6,FALSE\nBaBClF4,FALSE\nBaBSbS4,FALSE\nBaBiClO2,FALSE\nBaCaB2O5,FALSE\nBaCaSn3,TRUE\nBaCdSnS4,FALSE\nBaCu2SnSe4,FALSE\nBaCuSbS3,FALSE\nBaCuSbSe3,FALSE\nBaCuTeF,FALSE\nBaDy2CuO5,TRUE\nBaEu2Mn2O7,TRUE\nBaF2,FALSE\nBaGa2GeS6,FALSE\nBaGa2GeSe6,FALSE\nBaGa2SiS6,FALSE\nBaGa2SiSe6,FALSE\nBaGa2SnSe6,FALSE\nBaGa4S7,FALSE\nBaGa4Se7,FALSE\nBaGe2,FALSE\nBaGe3Pt,TRUE\nBaGe4(IrS3)2,FALSE\nBaGe4(IrSe3)2,FALSE\nBaGe4(RhSe3)2,FALSE\nBaHgS2,FALSE\nBaHgSe2,FALSE\nBaIn2(P2O7)2,FALSE\nBaIn2Ir,TRUE\nBaLa2CoS5,TRUE\nBaLa2In2S7,FALSE\nBaLa2In2Se7,FALSE\nBaLa2Te5O14,FALSE\nBaLi4,TRUE\nBaMn4O7,TRUE\nBaMn4ZnO8,TRUE\nBaMnO3,TRUE\nBaNa2GeS4,FALSE\nBaNa2GeSe4,FALSE\nBaNa2SnS4,FALSE\nBaNa2SnSe4,FALSE\nBaNaB5O9,FALSE\nBaNb4O6,TRUE\nBaO,FALSE\nBaPd(IO3)4,FALSE\nBaPdSe6,FALSE\nBaPrO3,FALSE\nBaPt5,TRUE\nBaReH9,FALSE\nBaS,FALSE\nBaSe,FALSE\nBaSi,TRUE\nBaSi2,FALSE\nBaSn2S5,FALSE\nBaSn3,TRUE\nBaSnO3,FALSE\nBaTaNO2,FALSE\nBaTbMn2O6,TRUE\nBaTe,FALSE\nBaTeMo2O9,FALSE\nBaTh3,TRUE\nBaTi14O28,TRUE\nBaTi4O7,TRUE\nBaTi4O8,TRUE\nBaTiO3,FALSE\nBaTl(MoO3)2,TRUE\nBaTl3,TRUE\nBaUSe3,FALSE\nBaV2SeO8,FALSE\nBaYb2O4,TRUE\nBaYbSn3,TRUE\nBaZn(MoO2)4,TRUE\nBaZn5,TRUE\nBaZnGeSe4,FALSE\nBaZnSO,FALSE\nBaZnSiSe4,FALSE\nBe12Pt,TRUE\nBe22Re,TRUE\nBe2HgTe,TRUE\nBe2W,TRUE\nBe3N2,FALSE\nBe3Sb2,FALSE\nBeAlB,TRUE\nBeCu,TRUE\nBeFe2Si,TRUE\nBeGaO3,TRUE\nBeGaRh2,TRUE\nBeO,FALSE\nBePd2,TRUE\nBePd3,TRUE\nBeS,FALSE\nBeSe,FALSE\nBeSiOs2,TRUE\nBeSiRu2,TRUE\nBeTcSe,TRUE\nBeTe,FALSE\nBi0.002Te0.003Pb0.999Se0.999,FALSE\nBi0.04Te0.06Pb0.98Se0.98,FALSE\nBi0.2Sb1.8Te3,FALSE\nBi0.2Te0.3Pb0.9Se0.9,FALSE\nBi0.4Sb1.6Te3,FALSE\nBi0.4Te0.6Pb0.8Se0.8,FALSE\nBi0.6Sb1.4Te3,FALSE\nBi1.4Sb0.6Te3,FALSE\nBi1.6Sb0.4Te3,FALSE\nBi1.8Sb0.2Te3,FALSE\nBi1.98Sb0.02Te3,FALSE\nBi12PO20,FALSE\nBi12Rh12O41,TRUE\nBi1Sb0.15,FALSE\nBi2(BO3)3,TRUE\nBi2(MoO4)3,FALSE\nBi2(PO4)3,TRUE\nBi24BO39,FALSE\nBi2AsClO4,FALSE\nBi2CO5,FALSE\nBi2I4O13,FALSE\nBi2Mo2Se2O13,FALSE\nBi2O3,FALSE\nBi2O5,TRUE\nBi2Pd3S2,TRUE\nBi2Pt,TRUE\nBi2S3,FALSE\nBi2SI2O11,FALSE\nBi2Se3,FALSE\nBi2SeI2O11,FALSE\nBi2Te0.03Se2.97,FALSE\nBi2Te0.1Se2.9,FALSE\nBi2Te0.3Se2.7,FALSE\nBi2Te0.45Se2.55,FALSE\nBi2Te0.4Se2.6,FALSE\nBi2Te0.6Se2.4,FALSE\nBi2Te0.9Se2.1,FALSE\nBi2Te1.2Se1.8,FALSE\nBi2Te1.5Se1.5,FALSE\nBi2Te2.1Se0.9,FALSE\nBi2Te2.4Se0.6,FALSE\nBi2Te2.7Se0.3,FALSE\nBi2Te2.97Se0.03,FALSE\nBi2Te2SO10,FALSE\nBi2Te2Se,FALSE\nBi2Te3,FALSE\nBi3BTeO9,FALSE\nBi3I4O13F3,FALSE\nBi3Se2NO11,FALSE\nBi4I,TRUE\nBi4Pb7Se13,FALSE\nBi4Pd(SeO3)4,FALSE\nBi5IO7,FALSE\nBi7O5F11,FALSE\nBi8Te7S5,FALSE\nBi9S6O7.5,FALSE\nBiAs2Os,TRUE\nBiBPbO4,FALSE\nBiBr3,FALSE\nBiBrO,FALSE\nBiClO,FALSE\nBiI3,FALSE\nBiIO,FALSE\nBiIO3F2,FALSE\nBiO,TRUE\nBiP3(PbO4)3,FALSE\nBiPO4,FALSE\nBiPb2S2I3,FALSE\nBiPbBrO2,FALSE\nBiPbClO2,FALSE\nBiPd,TRUE\nBiSBr,FALSE\nBiSCl,FALSE\nBiSI,FALSE\nBiSbTe3,FALSE\nBiSe,FALSE\nBiSeBr,FALSE\nBiSeI,FALSE\nBiSeO3F,FALSE\nBiTeI,FALSE\nBiTeNO6,FALSE\nCBr4,FALSE\nCI4,FALSE\nCa(AgGe)2,TRUE\nCa(Al4Co)2,TRUE\nCa(AlZn)2,TRUE\nCa(BC)2,TRUE\nCa(BIr)2,TRUE\nCa(BiO2)2,FALSE\nCa(CoGe)2,TRUE\nCa(CoS2)4,TRUE\nCa(GdS2)2,FALSE\nCa(GeRh)2,TRUE\nCa(LaS2)2,FALSE\nCa(MnAs)2,TRUE\nCa(NdS2)2,FALSE\nCa(Ni2O3)2,TRUE\nCa(PrS2)2,FALSE\nCa(SiPd)2,TRUE\nCa(SmS2)2,FALSE\nCa(TiS2)4,TRUE\nCa10Ge16(B2O17)3,FALSE\nCa11Bi10,TRUE\nCa11Ga7,TRUE\nCa2Bi2O5,FALSE\nCa2CdAs2,FALSE\nCa2CdPb,TRUE\nCa2Co9O13,TRUE\nCa2CuWO6,TRUE\nCa2Ge,FALSE\nCa2GeN2,TRUE\nCa2Mn9O13,TRUE\nCa2MnAlO5,TRUE\nCa2NiIrO6,TRUE\nCa2Os2O7,TRUE\nCa2PbAu2,TRUE\nCa2ScSbO6,FALSE\nCa2Si,FALSE\nCa2SmTaO6,FALSE\nCa2Sn,FALSE\nCa2Sn2F3,TRUE\nCa2SnS4,FALSE\nCa2Ti9O13,TRUE\nCa2TlCd,TRUE\nCa2ZnRh,TRUE\nCa3(BN2)2,FALSE\nCa3(GaPt)2,TRUE\nCa3Al2Ge3,TRUE\nCa3Au,TRUE\nCa3Au4,TRUE\nCa3Bi(PO4)3,FALSE\nCa3BiAs,TRUE\nCa3BiSb,TRUE\nCa3Cu2(ClO2)2,TRUE\nCa3In,TRUE\nCa3La2(SnS4)3,FALSE\nCa3N2,FALSE\nCa3PbN,TRUE\nCa3Sb2,FALSE\nCa3SbN,TRUE\nCa3Sn2S7,TRUE\nCa3Ti2(SiO4)3,FALSE\nCa3TlN,TRUE\nCa3Zr17O37,TRUE\nCa4Al3O10,TRUE\nCa4Bi6O13,FALSE\nCa5(Bi7O13)2,FALSE\nCa5Au2,TRUE\nCa5B3O9F,FALSE\nCa5Ir,TRUE\nCa5Sb3,TRUE\nCa5Sn4S13,TRUE\nCa6Ag16N,TRUE\nCa6Cu2Sn7,TRUE\nCaAgF5,TRUE\nCaAu5,TRUE\nCaB6,FALSE\nCaCdPd2,TRUE\nCaCdSi,TRUE\nCaCu5,TRUE\nCaEu2O3,TRUE\nCaEuO2,TRUE\nCaF2,FALSE\nCaGa3Ni2,TRUE\nCaGaAu3,TRUE\nCaGaGe,TRUE\nCaGe2,TRUE\nCaHfZn,TRUE\nCaHg2,TRUE\nCaI2,FALSE\nCaIn2Ir,TRUE\nCaIn4Ir,TRUE\nCaInAu,TRUE\nCaInPt,TRUE\nCaIrO3,TRUE\nCaMg2N2,FALSE\nCaMgSn,TRUE\nCaMnSn,TRUE\nCaNi5,TRUE\nCaO,FALSE\nCaOsO3,TRUE\nCaPb,TRUE\nCaPd3C,TRUE\nCaPrZn2,TRUE\nCaS,FALSE\nCaSe,FALSE\nCaSnO3,FALSE\nCaTaNO2,FALSE\nCaTe,FALSE\nCaTi4O8,TRUE\nCaTiO2,TRUE\nCaVO2,TRUE\nCaYbInSe4,TRUE\nCaZn2,TRUE\nCaZn3,TRUE\nCaZn3Ni2,TRUE\nCaZn5,TRUE\nCaZnSO,FALSE\nCd(GaS2)2,FALSE\nCd(GaSe2)2,FALSE\nCd(In15Te23)2,FALSE\nCd(InS2)2,FALSE\nCd(InSe2)2,FALSE\nCd(InTe2)2,FALSE\nCd(PS2)2,FALSE\nCd0.01Ga0.99Sb0.99Te0.01,FALSE\nCd0.01Hg0.99Se1,FALSE\nCd0.01In0.99Te0.01As0.99,FALSE\nCd0.02In0.98Te0.02As0.98,FALSE\nCd0.03In0.97Te0.03As0.97,FALSE\nCd0.04In0.96Te0.04As0.96,FALSE\nCd0.05Ga0.95Sb0.95Te0.05,FALSE\nCd0.05In0.95Te0.05As0.95,FALSE\nCd0.06In0.94Te0.06As0.94,FALSE\nCd0.07In0.93Te0.07As0.93,FALSE\nCd0.1Ga0.9Sb0.9Te0.1,FALSE\nCd0.1Hg0.9Se1,FALSE\nCd0.1In0.9Te0.1As0.9,FALSE\nCd0.204Hg0.796Te1,FALSE\nCd0.23Hg0.77Te1,FALSE\nCd0.28Hg0.72Te1,FALSE\nCd0.2Ga0.8Sb0.8Te0.2,FALSE\nCd0.2Hg0.8Se1,FALSE\nCd0.2In2.4Ag0.4Te4,FALSE\nCd0.35Hg0.65Te1,FALSE\nCd0.37Hg0.63Te1,FALSE\nCd0.3Hg0.7Se1,FALSE\nCd0.3Hg0.7Te1,FALSE\nCd0.4Hg0.6Se1,FALSE\nCd0.5Hg0.5Se1,FALSE\nCd0.5In2.25Ag0.25Te4,FALSE\nCd0.5In2.2Ag0.4Te4,FALSE\nCd0.6Hg0.4Se1,FALSE\nCd0.75In2.1Ag0.2Te4,FALSE\nCd0.7Hg0.3Se1,FALSE\nCd0.8Hg0.2Se1,FALSE\nCd0.8In2.1Ag0.1Te4,FALSE\nCd0.99Ga0.01Sb0.01Te0.99,FALSE\nCd0.99Hg0.01Se1,FALSE\nCd0.9Hg0.1Se1,FALSE\nCd12Ge17(B4O29)2,FALSE\nCd13I28,TRUE\nCd1Hg6.5As4Cl6,FALSE\nCd1Se0.01S0.99,FALSE\nCd1Se0.2S0.8,FALSE\nCd1Se0.35S0.65,FALSE\nCd1Se0.45S0.55,FALSE\nCd1Se0.65S0.35,FALSE\nCd1Se0.99S0.01,FALSE\nCd2AgRh,TRUE\nCd2InAgTe3,FALSE\nCd2InCuTe3,FALSE\nCd2InCuTe4,FALSE\nCd2PbO4,TRUE\nCd3AgPS6,FALSE\nCd3As2,FALSE\nCd3Bi(PO4)3,FALSE\nCd3Bi2,FALSE\nCd3In2(Te2S)2,FALSE\nCd3P2,FALSE\nCd3Sb2,FALSE\nCd3Te2MoO10,FALSE\nCd4As2Br3,FALSE\nCd4As2I3,FALSE\nCd4P2Br3,FALSE\nCd4P2Cl3,FALSE\nCd4P2I3,FALSE\nCd4Sb2I3,FALSE\nCd4Sb3,FALSE\nCd5Ga2(Te3S)2,FALSE\nCd6P7,FALSE\nCd8B5O15F,FALSE\nCdAg,TRUE\nCdAg2(PS3)2,FALSE\nCdAg2GeS4,FALSE\nCdAs2,FALSE\nCdAsPd5,TRUE\nCdAuO2,TRUE\nCdBiClO2,FALSE\nCdBr2,FALSE\nCdCl2,FALSE\nCdCu(SeO3)2,FALSE\nCdCu2GeS4,FALSE\nCdCu2GeSe4,FALSE\nCdCu2SnS4,FALSE\nCdCu2SnSe4,FALSE\nCdF2,FALSE\nCdGeAs2,FALSE\nCdGeP2,FALSE\nCdHIO4,FALSE\nCdHg4(AsI2)2,FALSE\nCdHg6(As2Br3)2,FALSE\nCdI2,FALSE\nCdIClO3,FALSE\nCdIn,FALSE\nCdIn8Te13,FALSE\nCdInCuSe3,FALSE\nCdO,FALSE\nCdP2,FALSE\nCdP4,FALSE\nCdP4PbO12,FALSE\nCdPd,TRUE\nCdPt,TRUE\nCdRhF6,TRUE\nCdS,FALSE\nCdSb,FALSE\nCdSb2Se3Br2,FALSE\nCdSb4MoO10,FALSE\nCdSe,FALSE\nCdSiAs2,FALSE\nCdSiP2,FALSE\nCdSnAs2,FALSE\nCdSnO3,FALSE\nCdSnP2,FALSE\nCdTe,FALSE\nCdTeO3,FALSE\nCe(AlZn)2,TRUE\nCe(BC)2,TRUE\nCe(CoAs)2,TRUE\nCe(CoB)4,TRUE\nCe(CuSb)2,TRUE\nCe(HO)3,TRUE\nCe(InS2)3,FALSE\nCe(MnGe)2,TRUE\nCe(MnSi)2,TRUE\nCe(PPt2)2,TRUE\nCe(SiAu)2,TRUE\nCe(SiNi)2,TRUE\nCe(SiPd)2,TRUE\nCe1.3Lu0.7S3,FALSE\nCe10Se14O,FALSE\nCe15B8N25,FALSE\nCe1Mn0.5Se1O1,FALSE\nCe2(SbPd3)3,TRUE\nCe2(SnSe3)3,FALSE\nCe2Al2Co15,TRUE\nCe2Co5B2,TRUE\nCe2CrN3,TRUE\nCe2Cu(NO)2,TRUE\nCe2Fe(SeO)2,FALSE\nCe2Fe17,TRUE\nCe2Ge2Se7,FALSE\nCe2GeSe5,FALSE\nCe2S2O,TRUE\nCe2S3,FALSE\nCe2Sb,TRUE\nCe2Se3,FALSE\nCe2SiSeO4,TRUE\nCe2Te3,FALSE\nCe2Ti2O7,TRUE\nCe2ZnNi2,TRUE\nCe3(Al3Ru)4,TRUE\nCe3Al,TRUE\nCe3AlC,TRUE\nCe3B2(ClO2)3,TRUE\nCe3In3Ru2,TRUE\nCe3LuSe6,FALSE\nCe3MnAlS7,TRUE\nCe3MoO7,FALSE\nCe3NbS3O4,TRUE\nCe3Pd5,TRUE\nCe3SiPt5,TRUE\nCe3Ta(ClO2)3,TRUE\nCe3TaO7,TRUE\nCe4(GeS4)3,FALSE\nCe4Bi3,TRUE\nCe4FeSe6O,TRUE\nCe4InSbSe9,FALSE\nCe4Si3Rh4,TRUE\nCe4Te7,FALSE\nCe5(SiN3)3,TRUE\nCe5CuSe8,TRUE\nCe5Ge3,TRUE\nCe5Si3,TRUE\nCe6B2(CBr)3,TRUE\nCe8Sb2S15,FALSE\nCe8U2O21,TRUE\nCe9SmO20,TRUE\nCeAgSn,TRUE\nCeAl2Pd5,TRUE\nCeAl2Pt3,TRUE\nCeAl3Ni2,TRUE\nCeAlO3,TRUE\nCeAlSi2,TRUE\nCeAsPd,TRUE\nCeAsSe,TRUE\nCeB2Ir3,TRUE\nCeBC,TRUE\nCeBiW2O9,FALSE\nCeCd2Ag,TRUE\nCeCdAu2,TRUE\nCeCoGeH,TRUE\nCeF3,FALSE\nCeGaO3,TRUE\nCeHSe,TRUE\nCeHg,TRUE\nCeInIr,TRUE\nCeIr5,TRUE\nCeLu3,TRUE\nCeMg2Ag,TRUE\nCeMgAg2,TRUE\nCeMgNi4,TRUE\nCeMgPt,TRUE\nCeMgZn2,TRUE\nCeMoO4F,FALSE\nCeN,FALSE\nCeNbO4,TRUE\nCeO2,FALSE\nCeOs2,TRUE\nCePd5,TRUE\nCePrO2,TRUE\nCeRh,TRUE\nCeSI,TRUE\nCeSbO3,TRUE\nCeScO3,FALSE\nCeSi2Ni,TRUE\nCeSi2Pt,TRUE\nCeSiI,TRUE\nCeSiIr,TRUE\nCeSiOs,TRUE\nCeTaN2O,FALSE\nCeTl2P2S7,FALSE\nCeTl3,TRUE\nCeTlZn,TRUE\nCeZnPO,TRUE\nCo(PO3)4,TRUE\nCo(WO4)2,TRUE\nCo1Te1.88,FALSE\nCo2B4Mo,TRUE\nCo2Ge,TRUE\nCo2O3,TRUE\nCo2Te3O8,FALSE\nCo3H,TRUE\nCo3Se4,TRUE\nCo3W,TRUE\nCo5Ge7,TRUE\nCo5RuO8,TRUE\nCo7Mo6,TRUE\nCo7Re17O48,TRUE\nCoAs3,FALSE\nCoAsRh,TRUE\nCoAsS,FALSE\nCoAsSe,FALSE\nCoCu2Sn,TRUE\nCoGe,TRUE\nCoH2(SN)4,TRUE\nCoMoP2,TRUE\nCoN,TRUE\nCoOF,TRUE\nCoP2,FALSE\nCoP3,FALSE\nCoPS,FALSE\nCoPbO3,TRUE\nCoSb2,FALSE\nCoSb3,FALSE\nCoSbS,FALSE\nCr(FeSe2)2,TRUE\nCr(MoS2)2,TRUE\nCr10Sb3Te7,TRUE\nCr2CuS4,TRUE\nCr2CuTe4,TRUE\nCr2GeC,TRUE\nCr2HO4,TRUE\nCr2HgSe4,TRUE\nCr2NiS4,TRUE\nCr2O3,FALSE\nCr2P3O11,TRUE\nCr2S3,FALSE\nCr2SbTe,TRUE\nCr3N2,TRUE\nCr3Ni(PO4)6,TRUE\nCr3P,TRUE\nCr3Se4,FALSE\nCr4As3,TRUE\nCr4Cu3Te8,TRUE\nCr7C3,TRUE\nCrAs,TRUE\nCrB2(PbO2)6,FALSE\nCrBi2I2O11,FALSE\nCrCo2Bi,TRUE\nCrCoGe,TRUE\nCrCoPt2,TRUE\nCrCu2Si,TRUE\nCrFe2Sb,TRUE\nCrFeP,TRUE\nCrH9(CN2)3,TRUE\nCrIrO4,TRUE\nCrIrO6,TRUE\nCrNi3,TRUE\nCrNiAs,TRUE\nCrNiP2O9,TRUE\nCrO2,FALSE\nCrO3,FALSE\nCrPbO4,FALSE\nCrSb2,FALSE\nCrSi2,FALSE\nCrTe2,FALSE\nCs(AsRu)2,TRUE\nCs(MoO3)3,TRUE\nCs0.4K0.6P1Se6,FALSE\nCs1.13Cd1.13Bi2.87Se6,FALSE\nCs1.43Cd1.43Bi2.57S6,FALSE\nCs10Cd4Sn4S17,FALSE\nCs2AgBiBr6,FALSE\nCs2AgBiCl6,FALSE\nCs2Al2B2O7,FALSE\nCs2Ba3(P2O7)2,FALSE\nCs2Cd(PSe3)2,FALSE\nCs2Cd0.25Hg5.75S7,FALSE\nCs2Cd1.35Hg4.65S7,FALSE\nCs2Cd2Bi2S5,FALSE\nCs2Cd3(B4O7)4,FALSE\nCs2Cd3Te4,FALSE\nCs2CrCl4,TRUE\nCs2Cu(PS3)3,FALSE\nCs2Cu2Sb2S5,FALSE\nCs2DyCu3Te4,FALSE\nCs2Ga2S5,FALSE\nCs2Ga2Se5,FALSE\nCs2Hg(ICl)2,FALSE\nCs2Hg3I8,FALSE\nCs2Hg3S4,FALSE\nCs2Hg6S7,FALSE\nCs2La1.19Bi8.81S16,FALSE\nCs2Li3(BO2)5,FALSE\nCs2MgGe3Se8,FALSE\nCs2MgSn3Se8,FALSE\nCs2Mo15S19,TRUE\nCs2NaCoF6,TRUE\nCs2NaMgF6,TRUE\nCs2NaMnF6,TRUE\nCs2NbCuSe4,FALSE\nCs2P2PdSe6,FALSE\nCs2PdSe8,FALSE\nCs2Pt(IO3)6,FALSE\nCs2SCl6F,TRUE\nCs2Sb,FALSE\nCs2SeClF6,TRUE\nCs2SiB4O9,FALSE\nCs2Sn(PSe3)2,FALSE\nCs2Sn3(SbS5)2,FALSE\nCs2Te,FALSE\nCs2TeBr6,FALSE\nCs2TeI6,FALSE\nCs2Th(PS3)3,FALSE\nCs2Ti(AgS2)2,FALSE\nCs2VAgS4,FALSE\nCs2Zn3(SeO3)4,FALSE\nCs2ZnGe3S8,FALSE\nCs2ZnGe3Se8,FALSE\nCs2ZnGe3Te8,FALSE\nCs2ZnSn3Se8,FALSE\nCs39Ga53(Se16Cl)6,FALSE\nCs3As,FALSE\nCs3Bi,FALSE\nCs3Bi2Br9,FALSE\nCs3Bi2I9,FALSE\nCs3Li4(BO2)7,FALSE\nCs3NaZn2Ge21,FALSE\nCs3Nb2AsSe11,FALSE\nCs3Nb9(TeO8)4,FALSE\nCs3PW3O13,FALSE\nCs3Sb,FALSE\nCs3Sb2Br9,FALSE\nCs3Sb2I9,FALSE\nCs3Sn3Cl7F2,FALSE\nCs3V2Cl9,TRUE\nCs4Ag9(SbS3)4,FALSE\nCs4BiAs3Se7,FALSE\nCs4Cu3Bi9S17,FALSE\nCs4Ga4Si19,FALSE\nCs4Ge(PSe3)4,FALSE\nCs4Ge5(PbS4)4,FALSE\nCs4In8GeSe16,FALSE\nCs4Zr3S14,FALSE\nCs5Bi(PSe3)4,FALSE\nCs5Mo21Se23,TRUE\nCs5P5Se12,FALSE\nCs6.4Na1.6Ga8Ge38,FALSE\nCsAg2AsS3,FALSE\nCsAg2TeS6,FALSE\nCsAg5Te3,FALSE\nCsAgCl3,TRUE\nCsAgSb4S7,FALSE\nCsAsSe2,FALSE\nCsAu,FALSE\nCsB3O5,FALSE\nCsBi2,FALSE\nCsBi3Se5,FALSE\nCsBiS2,FALSE\nCsBiSe2,FALSE\nCsBr,FALSE\nCsCaBO3,FALSE\nCsCaO3,TRUE\nCsCd4Ga5S12,FALSE\nCsCd4Ga5Se12,FALSE\nCsCd4Ga5Te12,FALSE\nCsCd4In5Se12,FALSE\nCsCd4In5Te12,FALSE\nCsCdBO3,FALSE\nCsCdInSe3,FALSE\nCsCeCdSe3,FALSE\nCsCeHgSe3,FALSE\nCsCl,FALSE\nCsCu(SbS2)2,FALSE\nCsCu2AsS3,FALSE\nCsCu2SbS3,FALSE\nCsDy9(Cd2Se9)2,FALSE\nCsEr9(Cd2Se9)2,FALSE\nCsErZnSe3,FALSE\nCsEuF3,TRUE\nCsF,FALSE\nCsGa(SnSe3)2,FALSE\nCsGa7,TRUE\nCsGaS3,FALSE\nCsGaSnSe4,FALSE\nCsGdO3,TRUE\nCsGdZnTe3,FALSE\nCsGe5BO12,FALSE\nCsGeB3O7,FALSE\nCsGeI3,FALSE\nCsH3(SeO3)2,FALSE\nCsHo9(Cd2Se9)2,FALSE\nCsI,FALSE\nCsIn(SnSe3)2,FALSE\nCsInGeS4,FALSE\nCsInGeSe4,FALSE\nCsInHgS3,FALSE\nCsInI3,TRUE\nCsInS2,FALSE\nCsInSe2,FALSE\nCsInSnS4,FALSE\nCsInTe2,FALSE\nCsInTe3O8,FALSE\nCsIr,TRUE\nCsIrO3,TRUE\nCsK(PSe4)2,FALSE\nCsK2Sb,FALSE\nCsLaHgSe3,FALSE\nCsLi(B3O5)2,FALSE\nCsLiCO3,FALSE\nCsLu7S11,FALSE\nCsLu7Se11,FALSE\nCsLuCoS3,FALSE\nCsMg149,TRUE\nCsMn4Ga5Te12,FALSE\nCsMn4In5Se12,FALSE\nCsMn4In5Te12,FALSE\nCsMnSb,TRUE\nCsNa2Sb,FALSE\nCsNa8(B7O12)3,FALSE\nCsNb6I11,TRUE\nCsNbSe2O7,FALSE\nCsNi2F6,TRUE\nCsPPbO4,FALSE\nCsPSe4,FALSE\nCsPSe6,FALSE\nCsRb(PSe4)2,FALSE\nCsRb2Sb,FALSE\nCsRbP,TRUE\nCsSb,FALSE\nCsSb(SO4)2,FALSE\nCsSbS2,FALSE\nCsSbSe2,FALSE\nCsSbTe2,FALSE\nCsSc(SeO3)2,FALSE\nCsScBr3,TRUE\nCsSmCdSe3,FALSE\nCsSmHgSe3,FALSE\nCsSmZnSe3,FALSE\nCsSn3,TRUE\nCsTa3(SeO6)2,FALSE\nCsTaPSe6,FALSE\nCsTb9(Cd2Se9)2,FALSE\nCsTbZnTe3,FALSE\nCsTiCl3,TRUE\nCsTiF4,TRUE\nCsTm9(Cd2Se9)2,FALSE\nCsUCuS3,TRUE\nCsVP2S7,TRUE\nCsWCl6,TRUE\nCsYCdSe3,FALSE\nCsYHgSe3,FALSE\nCsYTe3O8,FALSE\nCsYZnSe3,FALSE\nCsYbCoSe3,FALSE\nCsYbMnSe3,FALSE\nCsYbZnSe3,FALSE\nCsZn2B3O7,FALSE\nCsZn4In5Se12,FALSE\nCsZn4In5Te12,FALSE\nCsZrPSe6,FALSE\nCu(IrS2)2,TRUE\nCu(NO3)2,TRUE\nCu0.5Ge1Pb1.75S4,FALSE\nCu0.96Bi2Se3I1,FALSE\nCu1.8S1,FALSE\nCu10Sb3,TRUE\nCu11Sb4S13,TRUE\nCu15Si4,TRUE\nCu18S11,TRUE\nCu23(Sb4S13)2,TRUE\nCu25Se26,TRUE\nCu2GeS3,FALSE\nCu2GeSe3,FALSE\nCu2H3ClO3,TRUE\nCu2Hg2SF6,TRUE\nCu2HgGeSe4,TRUE\nCu2O,FALSE\nCu2OF2,TRUE\nCu2PHO5,TRUE\nCu2Sb,TRUE\nCu2Se,FALSE\nCu2SnSe3,FALSE\nCu2Te,FALSE\nCu2Te3O8,FALSE\nCu2WSe4,FALSE\nCu3(BiI4)4,TRUE\nCu3(P2O7)2,TRUE\nCu3AsS4,FALSE\nCu3AsSe4,FALSE\nCu3Bi6S10I,FALSE\nCu3Hg2(Te3O8)2,FALSE\nCu3Pd,TRUE\nCu3SbS4,FALSE\nCu3SbSe4,FALSE\nCu3Se2(ClO3)2,TRUE\nCu4As2O9,TRUE\nCu4H10SO12,TRUE\nCu4Pd,TRUE\nCu4Sn7S16,FALSE\nCu4W(SCl)4,TRUE\nCu5(Si2O7)2,TRUE\nCu6PbO8,TRUE\nCu7Hg6,TRUE\nCu8O,TRUE\nCu9O13,TRUE\nCu9S5,TRUE\nCu9Se4(Cl3O7)2,TRUE\nCuBS2,FALSE\nCuBi(PSe3)2,FALSE\nCuBiPbS3,FALSE\nCuBiPbSe3,FALSE\nCuBiSO,FALSE\nCuBiSeO,FALSE\nCuBr,FALSE\nCuCN2,TRUE\nCuCl,FALSE\nCuClO2,TRUE\nCuF,TRUE\nCuHg(SeO3)2,FALSE\nCuI,FALSE\nCuMoO4,TRUE\nCuN3,FALSE\nCuNi(CN)4,FALSE\nCuP2,FALSE\nCuP2(HO3)2,TRUE\nCuPO4F,TRUE\nCuPS3,FALSE\nCuPd,TRUE\nCuPtO2,TRUE\nCuSbPbS3,FALSE\nCuSbS2,FALSE\nCuSbSe2,FALSE\nCuSeO3,TRUE\nDy(Al2Cu)4,TRUE\nDy(CoGe)2,TRUE\nDy(CuSe)3,FALSE\nDy(CuSi)2,TRUE\nDy(CuTe)3,FALSE\nDy(GeRu)2,TRUE\nDy(InS2)3,FALSE\nDy12C6I17,TRUE\nDy12Co7,TRUE\nDy1Te1.4,FALSE\nDy1Te1.45,FALSE\nDy1Te1.7,FALSE\nDy2(GePt3)3,TRUE\nDy2(MoO4)3,FALSE\nDy2AlCo2,TRUE\nDy2C,TRUE\nDy2CdPd2,TRUE\nDy2CuOs,TRUE\nDy2MgIn,TRUE\nDy2MgTl,TRUE\nDy2Ni12P7,TRUE\nDy2O3,FALSE\nDy2S3,FALSE\nDy2Sn5,TRUE\nDy2Te3,FALSE\nDy2Ti3Si4,TRUE\nDy2TlCd,TRUE\nDy2ZnIn,TRUE\nDy3(CuGe)4,TRUE\nDy3Al0.5Si1S7,FALSE\nDy3Ga,TRUE\nDy3GaS6,FALSE\nDy3InC,TRUE\nDy3MnB7,TRUE\nDy4CdRh,TRUE\nDy4GaSbS9,FALSE\nDy4Sb3,TRUE\nDy4Te3S4,FALSE\nDy5Pb3,TRUE\nDy5Sn3,TRUE\nDy6FeTe2,TRUE\nDy7In(CoGe3)4,TRUE\nDyAg,TRUE\nDyAgGe,TRUE\nDyAgHg2,TRUE\nDyAs,FALSE\nDyB2Rh2C,TRUE\nDyB6,FALSE\nDyBPd3,TRUE\nDyBiPd,TRUE\nDyBiPt,TRUE\nDyCd2,TRUE\nDyCoSi2,TRUE\nDyFeSi,TRUE\nDyGe,TRUE\nDyInAu,TRUE\nDyInCu2,TRUE\nDyInPt2,TRUE\nDyIr2,TRUE\nDyMn2,TRUE\nDyN,FALSE\nDyNiGe2,TRUE\nDyNiSn,TRUE\nDyPO4,FALSE\nDyRh,TRUE\nDyS2,TRUE\nDySiIr,TRUE\nDySn3,TRUE\nDySnRu2,TRUE\nDyYAg2,TRUE\nDyZnGa,TRUE\nDyZnRh2,TRUE\nDyZrRu2,TRUE\nDyZrSb,TRUE\nEr(Al10Cr)2,TRUE\nEr(CrSi)2,TRUE\nEr(CuGe)2,TRUE\nEr(CuTe)3,FALSE\nEr(InS2)3,FALSE\nEr(ReO4)2,TRUE\nEr(SiPd)2,TRUE\nEr2(Ga3Co)3,TRUE\nEr2(MoO4)3,FALSE\nEr2C3,TRUE\nEr2Fe14B,TRUE\nEr2Mg3Ru,TRUE\nEr2MnC4,TRUE\nEr2O3,FALSE\nEr2Se3,FALSE\nEr2SnAu2,TRUE\nEr2Te3,FALSE\nEr3Al3NiGe2,TRUE\nEr3SnC,TRUE\nEr3Te4,FALSE\nEr4NiB13,TRUE\nEr5Bi3,TRUE\nEr5NiPb3,TRUE\nEr5Si3,TRUE\nEr6MnBi2,TRUE\nErAgSn,TRUE\nErAl9(Fe2Si3)2,TRUE\nErAlGe,TRUE\nErB2Ir3,TRUE\nErB2Ru3,TRUE\nErB6,FALSE\nErBPd3,TRUE\nErBiW2O9,FALSE\nErCu,TRUE\nErCuPb,TRUE\nErFeC2,TRUE\nErHg2,TRUE\nErLu3,TRUE\nErMg2,TRUE\nErN,FALSE\nErNi4Au,TRUE\nErNi4B,TRUE\nErNiSn,TRUE\nErPbAu,TRUE\nErRu3,TRUE\nErSe2,FALSE\nErSiPd,TRUE\nErSnAu,TRUE\nErTe,FALSE\nErTlPd,TRUE\nErZn12,TRUE\nEu(AlAu)2,TRUE\nEu(AsPd)2,TRUE\nEu(BiSe2)2,FALSE\nEu(BiTe2)2,FALSE\nEu(CdSb)2,TRUE\nEu(ClO4)3,TRUE\nEu(DySe2)2,FALSE\nEu(ErSe2)2,FALSE\nEu(FeSi)2,TRUE\nEu(GaS2)2,FALSE\nEu(GaSe2)2,FALSE\nEu(GaTe2)2,FALSE\nEu(HoSe2)2,FALSE\nEu(InAs)2,TRUE\nEu(InS2)2,FALSE\nEu(InSe2)2,FALSE\nEu(InTe2)2,FALSE\nEu(LuSe2)2,FALSE\nEu(MgBi)2,TRUE\nEu(MnGe)2,TRUE\nEu(Ni2B)6,TRUE\nEu(NiAs)2,TRUE\nEu(POs)2,TRUE\nEu(SbS2)2,FALSE\nEu(SbSe2)2,FALSE\nEu(TmSe2)2,FALSE\nEu(ZnGe)2,TRUE\nEu(ZnSi)2,TRUE\nEu1.75Ag0.5Ge1S4,FALSE\nEu1.83Ta15O32,FALSE\nEu2(Ga3Rh)3,TRUE\nEu2C(NO)2,TRUE\nEu2CuO4,TRUE\nEu2Ga2GeS7,FALSE\nEu2Ge(BO4)2,TRUE\nEu2O3,FALSE\nEu2PBr,TRUE\nEu2ReO5,TRUE\nEu2Se3,FALSE\nEu2SnSe5,FALSE\nEu2TeO2,TRUE\nEu3(InP2)2,FALSE\nEu3As2,FALSE\nEu3BWO9,TRUE\nEu3Bi4S9,FALSE\nEu3P2,FALSE\nEu3S4,FALSE\nEu3Sb4S9,FALSE\nEu3Sb4Se9,FALSE\nEu3Se4,FALSE\nEu3Sn,TRUE\nEu4Te7,FALSE\nEu7(Ga3Sb4)2,FALSE\nEuAgSb,TRUE\nEuAl2O4,FALSE\nEuAlO3,TRUE\nEuB(SbO4)2,FALSE\nEuBi3,TRUE\nEuBiW2O9,FALSE\nEuCd11,TRUE\nEuClO,TRUE\nEuCo8P5,TRUE\nEuCu2SnS4,FALSE\nEuCu9Sn4,TRUE\nEuCuSeF,TRUE\nEuCuSeO,TRUE\nEuF3,TRUE\nEuGe3Pt,TRUE\nEuH2,FALSE\nEuIn2(GeIr)4,FALSE\nEuN,FALSE\nEuNiGe3,TRUE\nEuO,FALSE\nEuPPt,TRUE\nEuPd,TRUE\nEuRhO3,TRUE\nEuS,FALSE\nEuSb4S7,FALSE\nEuSb4Te7,FALSE\nEuSbO3,TRUE\nEuScO3,TRUE\nEuSe,FALSE\nEuSeClO3,TRUE\nEuSn3,TRUE\nEuSnAu2,TRUE\nEuSnO3,TRUE\nEuSnTe2,FALSE\nEuTe,FALSE\nEuTiClO3,TRUE\nEuTiO3,TRUE\nEuTl,TRUE\nEuVO4,FALSE\nEuZn,TRUE\nFe(PdSe)2,TRUE\nFe10O9F11,TRUE\nFe12As5,TRUE\nFe2B(PO4)3,FALSE\nFe2Cu(PO4)3,TRUE\nFe2O2F3,TRUE\nFe2O3,FALSE\nFe2S,TRUE\nFe2Te3,FALSE\nFe3B,TRUE\nFe3N,TRUE\nFe3Si,TRUE\nFe4H15(IO8)3,FALSE\nFe4O7F,TRUE\nFe4Si2Sn7O16,TRUE\nFe6O7F5,TRUE\nFe6W6C,TRUE\nFe9Co7,TRUE\nFeAg3(CN)6,TRUE\nFeAgSe2,FALSE\nFeAgTe2,FALSE\nFeAs2O7,TRUE\nFeAsS,FALSE\nFeAsSe,FALSE\nFeBi(SeO3)3,FALSE\nFeBi25O39,FALSE\nFeCo2Si,TRUE\nFeCoAs,TRUE\nFeCuS2,FALSE\nFeCuSe2,FALSE\nFeCuTe2,FALSE\nFeI2,FALSE\nFeOF,TRUE\nFeP,TRUE\nFeP4,FALSE\nFePS,FALSE\nFePd3,TRUE\nFeRhO3,TRUE\nFeSi2,FALSE\nFeSn,TRUE\nGa1As0.1P0.9,FALSE\nGa0.001Te1Pb0.999,FALSE\nGa0.005Te1Pb0.995,FALSE\nGa0.01Te1Pb0.99,FALSE\nGa0.04Te1Pb0.96,FALSE\nGa0.07Te1Pb0.93,FALSE\nGa0.95Hg0.05Sb0.95Te0.05,FALSE\nGa0.99Hg0.01Sb0.99Te0.01,FALSE\nGa0.9Hg0.1Sb0.9Te0.1,FALSE\nGa1.001Sb0.999Se0.003,FALSE\nGa1.001Sb0.999Te0.003,FALSE\nGa1.002Sb0.998Se0.006,FALSE\nGa1.002Sb0.998Te0.006,FALSE\nGa1.005Sb0.995Se0.015,FALSE\nGa1.005Sb0.995Te0.015,FALSE\nGa1.01Cu0.99Se2.01,FALSE\nGa1.01Sb0.99Se0.03,FALSE\nGa1.01Sb0.99Te0.03,FALSE\nGa1.02Sb0.98Se0.06,FALSE\nGa1.02Sb0.98Te0.06,FALSE\nGa1.05Sb0.95Se0.15,FALSE\nGa1.05Sb0.95Te0.15,FALSE\nGa1.1Cu0.9Se2.1,FALSE\nGa1.1Sb0.9Se0.3,FALSE\nGa1.1Sb0.9Te0.3,FALSE\nGa1.2Cu0.8Se2.2,FALSE\nGa1.5Cu0.5S2.5,FALSE\nGa1.5Cu0.5Se2.5,FALSE\nGa1.65Cu0.35S2.65,FALSE\nGa1.65Cu0.35Se2.65,FALSE\nGa1.6Cu0.4S2.6,FALSE\nGa1.7Cu0.3S2.7,FALSE\nGa1.85Cu0.15Se2.85,FALSE\nGa1.8Cu0.2S2.8,FALSE\nGa1.8Cu0.2Se2.8,FALSE\nGa1.95Cu0.05S2.95,FALSE\nGa1.95Cu0.05Se2.95,FALSE\nGa1.99Cu0.01Se2.99,FALSE\nGa1.9Cu0.1S2.9,FALSE\nGa1As0.01P0.99,FALSE\nGa1As0.2P0.8,FALSE\nGa1As0.3P0.7,FALSE\nGa1As0.4P0.6,FALSE\nGa1As0.5P0.5,FALSE\nGa1As0.6P0.4,FALSE\nGa1As0.7P0.3,FALSE\nGa1As0.8P0.2,FALSE\nGa1As0.99P0.01,FALSE\nGa1As0.9P0.1,FALSE\nGa1Sb0.01As0.99,FALSE\nGa1Sb0.14As0.86,FALSE\nGa1Sb0.25As0.75,FALSE\nGa1Sb0.35As0.65,FALSE\nGa1Sb0.3As0.7,FALSE\nGa1Sb0.85As0.15,FALSE\nGa1Sb0.8As0.2,FALSE\nGa1Sb0.95As0.05,FALSE\nGa1Sb0.99As0.01,FALSE\nGa2(TeO3)3,FALSE\nGa2Cu1S3.5,FALSE\nGa2CuSe4,FALSE\nGa2GePbSe6,FALSE\nGa2GeTe3,FALSE\nGa2HgS4,FALSE\nGa2HgSe4,FALSE\nGa2NiS4,TRUE\nGa2O3,FALSE\nGa2PbS4,FALSE\nGa2PbSe4,FALSE\nGa2S3,FALSE\nGa2Se2O7,FALSE\nGa2Se3,FALSE\nGa2Si(AgS3)2,FALSE\nGa2SiPbSe6,FALSE\nGa2SnGeS6,FALSE\nGa2Te3,FALSE\nGa3CuSe5,FALSE\nGa3CuTe5,FALSE\nGa3Pt2,TRUE\nGa3SiAg3Se8,FALSE\nGa4Cu2Te7,FALSE\nGa4PbS7,FALSE\nGa4SnS7,FALSE\nGa4SnSe7,FALSE\nGa5Ge(PbS3)4,FALSE\nGa5Ge(PbSe3)4,FALSE\nGa5Pd13,TRUE\nGa8Cu3Mo2,TRUE\nGa9Rh2,TRUE\nGaAgGe3Se8,FALSE\nGaAgGe5Se12,FALSE\nGaAgGeS4,FALSE\nGaAgO2,FALSE\nGaAgS2,FALSE\nGaAgSe2,FALSE\nGaAgTe2,FALSE\nGaAs,FALSE\nGaAs2W,TRUE\nGaBi,FALSE\nGaBi25O39,FALSE\nGaCuGeSe4,FALSE\nGaCuO2,FALSE\nGaCuS2,FALSE\nGaCuSe2,FALSE\nGaCuTe2,FALSE\nGaFe3,TRUE\nGaFeNi2,TRUE\nGaGeTe,FALSE\nGaHSeO4,FALSE\nGaN,FALSE\nGaP,FALSE\nGaS,FALSE\nGaSb,FALSE\nGaSe,FALSE\nGaSiAgSe4,FALSE\nGaSiRu2,TRUE\nGaTc,FALSE\nGaTc2W,TRUE\nGaTe,FALSE\nGd(CuS)3,FALSE\nGd(CuSe)3,FALSE\nGd(CuTe)3,FALSE\nGd(InS2)3,FALSE\nGd(NiGe)2,TRUE\nGd(SiRu)2,TRUE\nGd1.05Sc0.95Se3,FALSE\nGd1.47Mn2.04In0.49S5,FALSE\nGd1.87Lu2.13Se6,FALSE\nGd1Mn1.95In1.05S5,FALSE\nGd2(MoO4)3,FALSE\nGd2(Zn2Ge)3,TRUE\nGd2AlCo2,TRUE\nGd2Mn4S7,FALSE\nGd2O3,FALSE\nGd2S3,FALSE\nGd2Se3,FALSE\nGd2Te3,FALSE\nGd2Zn17,TRUE\nGd2ZrS5,FALSE\nGd3(AlNi3)2,TRUE\nGd3.04Sc0.96S6,FALSE\nGd3Al0.74Si0.7S7,FALSE\nGd3Al7Ag2,TRUE\nGd3Co11B4,TRUE\nGd3ReO7,TRUE\nGd3S4,TRUE\nGd4GaSbS9,FALSE\nGd6Ge2.5S14,FALSE\nGd6Ta4Al43,TRUE\nGdAs,FALSE\nGdB(SbO4)2,FALSE\nGdB6,FALSE\nGdB66,FALSE\nGdCd2,TRUE\nGdCd4B3O10,FALSE\nGdGeRu,TRUE\nGdH2NO5,FALSE\nGdInIr,TRUE\nGdN,FALSE\nGdNiO3,TRUE\nGdO2,TRUE\nGdPbAu,TRUE\nGdSb,TRUE\nGdSbPd,TRUE\nGdScS3,FALSE\nGdSe2,TRUE\nGdTe,FALSE\nGdZn,TRUE\nGdZnIn,TRUE\nGe(Bi3O5)4,FALSE\nGe(SeO3)2,FALSE\nGe(WO3)6,TRUE\nGe0.01Pb0.99Se1,FALSE\nGe0.01Te0.01Pb0.99Se0.99,FALSE\nGe0.01Te0.99Pb0.99S0.01,FALSE\nGe0.01Te1Pb0.99,FALSE\nGe0.02Te0.98Pb0.98S0.02,FALSE\nGe0.03Pb0.97Se0.97S0.03,FALSE\nGe0.05Pb0.95Se0.95S0.05,FALSE\nGe0.05Pb0.95Se1,FALSE\nGe0.05Te0.95Pb0.95S0.05,FALSE\nGe0.05Te1Pb0.95,FALSE\nGe0.06Te0.06Pb0.94Se0.94,FALSE\nGe0.15Pb0.85Se0.85S0.15,FALSE\nGe0.15Te0.15Pb0.85Se0.85,FALSE\nGe0.15Te1Pb0.85,FALSE\nGe0.1Pb0.9Se0.9S0.1,FALSE\nGe0.1Pb0.9Se1,FALSE\nGe0.1Te1Pb0.9,FALSE\nGe0.25Te1Pb0.75,FALSE\nGe0.2Pb0.8Se1,FALSE\nGe0.2Te0.2Pb0.8Se0.8,FALSE\nGe0.2Te1Pb0.8,FALSE\nGe0.39Te1Pb0.61,FALSE\nGe0.3Pb0.7Se1,FALSE\nGe0.3Te1Pb0.7,FALSE\nGe0.41Te1Pb0.59,FALSE\nGe0.4Te1Pb0.6,FALSE\nGe2Os,TRUE\nGe2Sb2Te5,FALSE\nGe3Bi3O10.5,FALSE\nGe3Ru2,FALSE\nGe3Sb,TRUE\nGe40Te5.3I8,FALSE\nGe5(Te4As)2,TRUE\nGeAs,FALSE\nGeAs2,FALSE\nGeAs3,TRUE\nGeI2,FALSE\nGeO2,FALSE\nGeP,FALSE\nGePb2(SeO3)4,FALSE\nGePbS3,FALSE\nGePt2,TRUE\nGeRh,TRUE\nGeS,FALSE\nGeS2,FALSE\nGeSe,FALSE\nGeSe2,FALSE\nGeTe2,FALSE\nH2Se,TRUE\nH6Pt(I3O10)2,FALSE\nH7Se2NO6,FALSE\nHPbI3,TRUE\nHf(CoSi)2,TRUE\nHf(CuP)2,TRUE\nHf(VGa2)2,TRUE\nHf(VH2)2,TRUE\nHf2Al3C4,TRUE\nHf2Co4P3,TRUE\nHf2Fe,TRUE\nHf2Ge,TRUE\nHf2Hg,TRUE\nHf2MnIr,TRUE\nHf2Ni,TRUE\nHf2OsPd,TRUE\nHf2ReRh,TRUE\nHf2S,TRUE\nHf2Si,TRUE\nHf2Tl,TRUE\nHf3(CuSi)4,TRUE\nHf3(NiGe)4,TRUE\nHf3P,TRUE\nHf3P3Pd4,TRUE\nHf3Sb,TRUE\nHf3Zn3N,TRUE\nHf4Al3,TRUE\nHf4Co4Si7,TRUE\nHf54Os17,TRUE\nHf5CuPb3,TRUE\nHf5Pb,TRUE\nHf5Sb3,TRUE\nHf5Sb9,TRUE\nHf5Si4,TRUE\nHf5Sn3,TRUE\nHf5Sn4,TRUE\nHf5Te4,TRUE\nHf6PbO18,TRUE\nHf7P4,TRUE\nHfAlPd2,TRUE\nHfAs2,TRUE\nHfAsRh,TRUE\nHfB,TRUE\nHfB4Ir3,TRUE\nHfC,TRUE\nHfCo3B2,TRUE\nHfFe2,TRUE\nHfGaCo2,TRUE\nHfHg4(AsCl3)2,FALSE\nHfHg4(PCl3)2,FALSE\nHfInCu2,TRUE\nHfNi5,TRUE\nHfO2,FALSE\nHfOs2,TRUE\nHfPt,TRUE\nHfS2,FALSE\nHfS3,FALSE\nHfSe2,FALSE\nHfSi,TRUE\nHfSiPt,TRUE\nHfTc,TRUE\nHfTiF6,TRUE\nHfTl3,TRUE\nHfVSi,TRUE\nHfZnNi2,TRUE\nHg2Rh,TRUE\nHg2Sb2O7,TRUE\nHg3As,TRUE\nHg3Bi2(SCl4)2,FALSE\nHg3Bi2(TeCl4)2,FALSE\nHg3C,TRUE\nHg3PS3,FALSE\nHg3PS4,FALSE\nHg3Sb,TRUE\nHg5AsS2I3,FALSE\nHg7.5As4Cl6,FALSE\nHg8Bi3As4Cl13,FALSE\nHgBr,FALSE\nHgBr2,FALSE\nHgBrCl,FALSE\nHgCl,FALSE\nHgCl2,FALSE\nHgI,FALSE\nHgIrO3,TRUE\nHgO,FALSE\nHgOsPb2,TRUE\nHgPS3,FALSE\nHgPt,TRUE\nHgPt3,TRUE\nHgRhO3,TRUE\nHgS,FALSE\nHgSe,FALSE\nHgTe,FALSE\nHgTeBr,FALSE\nHgTeI,FALSE\nHo(BC)2,TRUE\nHo(BiO3)2,TRUE\nHo(CuO2)2,TRUE\nHo(CuSe)3,FALSE\nHo(CuTe)3,FALSE\nHo(InS2)3,FALSE\nHo(MnSn)6,TRUE\nHo(NiB)2,TRUE\nHo(SbO3)2,TRUE\nHo(SiOs)2,TRUE\nHo(SiPd)2,TRUE\nHo(SiPt)2,TRUE\nHo(SiRu)2,TRUE\nHo10Si17,TRUE\nHo2(MoO4)3,FALSE\nHo2Au,TRUE\nHo2B4C,TRUE\nHo2Co17,TRUE\nHo2CuRh,TRUE\nHo2Ge5Rh3,TRUE\nHo2GeS5,FALSE\nHo2HfS5,FALSE\nHo2O3,FALSE\nHo2Pd2Pb,TRUE\nHo2S3,FALSE\nHo3AlC,TRUE\nHo3GaC,TRUE\nHo3Ge5,TRUE\nHo3Hg,TRUE\nHo3Ni19B10,TRUE\nHo3P,TRUE\nHo3Pd2,TRUE\nHo4C7,TRUE\nHo4Ga16Co3,TRUE\nHo5(Ge5Rh2)2,TRUE\nHo5Si4,TRUE\nHoAlAu2,TRUE\nHoAlB14,TRUE\nHoB2Rh3,TRUE\nHoB4,TRUE\nHoC2,TRUE\nHoCd,TRUE\nHoCd3,TRUE\nHoCdCu4,TRUE\nHoCo3,TRUE\nHoCu4Pd,TRUE\nHoGe,TRUE\nHoGeAu,TRUE\nHoInAu2,TRUE\nHoInPt,TRUE\nHoMg2,TRUE\nHoMgAu2,TRUE\nHoMgZn2,TRUE\nHoMn12,TRUE\nHoN,FALSE\nHoNiGe,TRUE\nHoSb2,TRUE\nHoSi,TRUE\nHoSiRu2C,TRUE\nHoTh3,TRUE\nHoTiGe,TRUE\nHoTiO3,TRUE\nHoTiSi,TRUE\nHoTlPd,TRUE\nHoZnRh,TRUE\nHoZnRh2,TRUE\nICl2,TRUE\nIn(MoSe)3,TRUE\nIn(PS2)2,FALSE\nIn(PSe2)2,FALSE\nIn0.001Te1Pb0.999,FALSE\nIn0.005Te1Pb0.995,FALSE\nIn0.01Ga0.99As0.99P0.01,FALSE\nIn0.01Ga0.99As1,FALSE\nIn0.01Te1Pb0.99,FALSE\nIn0.04Te1Pb0.96,FALSE\nIn0.07Te1Pb0.93,FALSE\nIn0.1Ga0.9As0.1P0.9,FALSE\nIn0.1Ga0.9As0.9P0.1,FALSE\nIn0.2Ga0.8As0.2P0.8,FALSE\nIn0.2Ga0.8As0.8P0.2,FALSE\nIn0.2Ga0.8As1,FALSE\nIn0.3Ga0.7As0.3P0.7,FALSE\nIn0.3Ga0.7As0.7P0.3,FALSE\nIn0.3Ga0.7As1,FALSE\nIn0.3Ga0.7P1,FALSE\nIn0.4Ga0.6As0.4P0.6,FALSE\nIn0.4Ga0.6As0.6P0.4,FALSE\nIn0.4Ga0.6As1,FALSE\nIn0.4Ga0.6P1,FALSE\nIn0.4Ga1.6Cu1S3.5,FALSE\nIn0.5Ga0.5As0.5P0.5,FALSE\nIn0.5Ga0.5As1,FALSE\nIn0.5Ga0.5P1,FALSE\nIn0.6Ga0.4As0.6P0.4,FALSE\nIn0.72Ga0.28As1,FALSE\nIn0.7Ga0.3As0.3P0.7,FALSE\nIn0.8Ga0.2As0.2P0.8,FALSE\nIn0.8Ga0.2As0.8P0.2,FALSE\nIn0.8Ga0.2As1,FALSE\nIn0.99Ga0.01As0.01P0.99,FALSE\nIn0.99Ga0.01As0.99P0.01,FALSE\nIn0.9Ga0.1As0.1P0.9,FALSE\nIn0.9Ga0.1As0.9P0.1,FALSE\nIn1.01Cu0.99Se2.01,FALSE\nIn1.05Cu0.95Se2.05,FALSE\nIn1.1Cu0.9Se2.1,FALSE\nIn1.3Cu0.7Se2.3,FALSE\nIn1.5Cu0.5Se2.5,FALSE\nIn1.65Cu0.35Se2.65,FALSE\nIn1.6Cu0.4Se2.6,FALSE\nIn1.6Ga0.4Cu1S3.5,FALSE\nIn1.7Cu0.3Se2.7,FALSE\nIn1.85Cu0.15Se2.85,FALSE\nIn1.8Cu0.2Se2.8,FALSE\nIn1.99Cu0.01Se2.99,FALSE\nIn1.9Cu0.1Se2.9,FALSE\nIn11.3Bi14.7S38,FALSE\nIn11Cu9Se20,TRUE\nIn1Ag1.75Sb5.75Se11,FALSE\nIn1Ga1Cu1S3.5,FALSE\nIn1Hg4As2.5Br3.5,FALSE\nIn1Sb0.01As0.99,FALSE\nIn1Sb0.1As0.9,FALSE\nIn1Sb0.2As0.8,FALSE\nIn1Sb0.3As0.7,FALSE\nIn1Sb0.4As0.6,FALSE\nIn1Sb0.5As0.5,FALSE\nIn1Sb0.6As0.4,FALSE\nIn1Sb0.7As0.3,FALSE\nIn1Sb0.8As0.2,FALSE\nIn1Sb0.99As0.01,FALSE\nIn1Sb0.9As0.1,FALSE\nIn2As2Cl2O5,FALSE\nIn2B(PO4)3,FALSE\nIn2Bi3Se7I,FALSE\nIn2Co,TRUE\nIn2Cu1S3.5,FALSE\nIn2FeSe4,FALSE\nIn2GeTe3,FALSE\nIn2Hg6(P2Cl3)3,FALSE\nIn2HgS4,FALSE\nIn2HgSe4,FALSE\nIn2HgTe4,FALSE\nIn2O3,FALSE\nIn2Pt,TRUE\nIn2S3,FALSE\nIn2Se,FALSE\nIn2Se2O7,FALSE\nIn2Se3,FALSE\nIn2Te,FALSE\nIn3AgTe5,FALSE\nIn3Au10,TRUE\nIn3Bi7(Pb2S9)2,TRUE\nIn3CuS5,FALSE\nIn3CuSe5,FALSE\nIn3CuTe5,FALSE\nIn3Pd5,TRUE\nIn3Sb,TRUE\nIn4As5(BrO4)3,FALSE\nIn4Bi3S10,FALSE\nIn4Cu2Te7,FALSE\nIn4S5,FALSE\nIn4Se3,FALSE\nIn4Te3,FALSE\nIn5AgS8,FALSE\nIn5AgTe8,FALSE\nIn5CuS8,FALSE\nIn5Se6,FALSE\nIn6S7,FALSE\nIn6Se7,FALSE\nIn9AgTe14,FALSE\nInAg3,TRUE\nInAgO2,FALSE\nInAgS2,FALSE\nInAgSe2,FALSE\nInAgTe2,FALSE\nInAs,FALSE\nInAsI,FALSE\nInAu3,TRUE\nInBi2S4Br,FALSE\nInBi2S4Cl,FALSE\nInBi2Se4Br,FALSE\nInCuGeSe4,FALSE\nInCuS2,FALSE\nInCuSe2,FALSE\nInCuTe2,FALSE\nInFe2CuSe4,TRUE\nInHg7S6Cl5,FALSE\nInHgW2,TRUE\nInN,FALSE\nInP,FALSE\nInPS4,FALSE\nInPt,TRUE\nInPt3C,TRUE\nInS,FALSE\nInSb,FALSE\nInSb2S4Br,FALSE\nInSb2S4Cl,FALSE\nInSb2Se4Br,FALSE\nInSe,FALSE\nInSiIr,TRUE\nInSiTe3,TRUE\nInSn2As2Se,FALSE\nInSnAsSe,FALSE\nIr0.67S2,FALSE\nIr0.67Se2,FALSE\nIrPb,TRUE\nIrS2,FALSE\nIrSe2,FALSE\nIrSeS,FALSE\nK(CoSe)2,TRUE\nK(FeAs)2,TRUE\nK(GeSe2)2,FALSE\nK(OsO3)2,TRUE\nK0.8Sn2Hg1.2S8,FALSE\nK1.25Bi7.25Pb3.5Se15,FALSE\nK1.46Sn3.09Bi7.45Se15,FALSE\nK1.83Cd1.83Bi2.17S6,FALSE\nK10Co4Sn4S17,FALSE\nK10Fe4Sn4S17,FALSE\nK10Mn4Sn4S17,FALSE\nK10Sn3(PSe3)8,FALSE\nK10Zn4Ge4S17,FALSE\nK10Zn4Sn4S17,FALSE\nK11Mn4O16,TRUE\nK2.15Sb8.15Pb1.7Se15,FALSE\nK2Ag3Sb3S7,FALSE\nK2AgSnSe4,FALSE\nK2Al2B2O7,FALSE\nK2Au(IO3)5,FALSE\nK2B10H9O,TRUE\nK2BaNb2S11,FALSE\nK2Bi8Se13,FALSE\nK2Cd(PSe3)2,FALSE\nK2Cd2Te3,FALSE\nK2Cd3S4,FALSE\nK2Cd3Se4,FALSE\nK2Cd3Te4,FALSE\nK2Ce(PO4)2,FALSE\nK2Dy2Ti3O10,FALSE\nK2FeGe3Se8,FALSE\nK2Ga3CuSe6,FALSE\nK2Gd2Sb2Se9,FALSE\nK2Gd2Ti3O10,FALSE\nK2Ge2PbS6,FALSE\nK2Ge3(BO5)2,FALSE\nK2Hg(PSe3)2,FALSE\nK2Hg3(GeS4)2,FALSE\nK2Hg3Se1.31S2.69,FALSE\nK2Hg3Se2.97S1.03,FALSE\nK2Ho4Cu4S9,FALSE\nK2In2P3Se10,FALSE\nK2In3AgSe6,FALSE\nK2In3CuSe6,FALSE\nK2La2Sb2S9,FALSE\nK2La2Ti3O10,FALSE\nK2Mn(SnSe3)2,FALSE\nK2Mn3S4,TRUE\nK2MnSnSe4,FALSE\nK2Mo2Se2O11,FALSE\nK2NbCuS4,FALSE\nK2NbCuSe4,FALSE\nK2NbO6,TRUE\nK2Nd2Ti3O10,FALSE\nK2PAuS4,FALSE\nK2PdSe10,FALSE\nK2RbSb,FALSE\nK2ReH9,FALSE\nK2RuCl6,TRUE\nK2S,FALSE\nK2Sb8Se3,FALSE\nK2Se,FALSE\nK2Sm2Ti3O10,FALSE\nK2SmP2S7,FALSE\nK2Sn(AuS2)2,FALSE\nK2Sn2Hg3S8,FALSE\nK2Sn3(SbS5)2,FALSE\nK2Ta15O32,FALSE\nK2Te,FALSE\nK2TeI6,FALSE\nK2Th(CuS2)2,FALSE\nK2Ti(CuS2)2,FALSE\nK2VAgS4,FALSE\nK2VCuS4,FALSE\nK2Zn(SnSe3)2,FALSE\nK2ZnSn3S8,FALSE\nK2ZnTe2,FALSE\nK3(FeS2)2,TRUE\nK3B6ClO10,FALSE\nK3Bi2I9,FALSE\nK3Cd(BO2)5,FALSE\nK3Cr2(PS4)3,FALSE\nK3Ga3Ge7S20,FALSE\nK3Ga3Ge7Se20,FALSE\nK3Hg,TRUE\nK3LiNb6O15,TRUE\nK3NaSn3Se8,FALSE\nK3Nb2AsSe11,FALSE\nK3Sm(AsS4)2,FALSE\nK3Sn,TRUE\nK3Ta2AsS11,FALSE\nK3Ta2AsSe11,FALSE\nK3Th2Cu3S7,FALSE\nK3Ti2P5S18,FALSE\nK3UF3,TRUE\nK3V,TRUE\nK4(ZrSe5)3,FALSE\nK4Ag9(SbS3)4,FALSE\nK4Al4Si19,FALSE\nK4C2O3,TRUE\nK4Ce3Sn3S14,FALSE\nK4Ga4Si19,FALSE\nK4Ge(PSe3)4,FALSE\nK4GeS4,FALSE\nK4GeSe4,FALSE\nK4Hf3Se14,FALSE\nK4Nb2S11,FALSE\nK5In3P6Se19,FALSE\nK6Cd4Sn3Se13,FALSE\nK6CdTe4,FALSE\nK6Ta1.03Nb2.97S25,FALSE\nK6Ta2.93Nb1.07S22,FALSE\nK6Yb3(PS4)5,FALSE\nK8Ce2I18O53,FALSE\nK8N3O,TRUE\nK9Bi13S24,FALSE\nKAg2,TRUE\nKAg2AsS3,FALSE\nKAg2PS4,FALSE\nKAg2SbS3,FALSE\nKAg2SbS4,FALSE\nKAgAsS2,FALSE\nKAgF3,TRUE\nKAgO,TRUE\nKAlGeS4,FALSE\nKAsSe2,FALSE\nKAu(IO3)4,FALSE\nKB5PbO9,FALSE\nKBaAsSe3,FALSE\nKBaB5O9,FALSE\nKBaSbSe3,FALSE\nKBi2,TRUE\nKBi3S5,FALSE\nKBiO3,TRUE\nKBiS2,FALSE\nKBiSe2,FALSE\nKBr,FALSE\nKC60,TRUE\nKCd4Ga5Se12,FALSE\nKCeSe4,FALSE\nKCl,FALSE\nKCoO2,TRUE\nKCu2BiS3,FALSE\nKCu2SbS3,FALSE\nKCu3S2,FALSE\nKCu4AsS4,FALSE\nKCuPO4,TRUE\nKCuSnS3,FALSE\nKCuSnSe3,FALSE\nKEuAsS4,FALSE\nKEuS2,TRUE\nKF,FALSE\nKFe2BiO5,FALSE\nKFeCuTe2,FALSE\nKGaSe2,FALSE\nKGaSnSe4,FALSE\nKH(CN2)3,TRUE\nKH3(SeO3)2,FALSE\nKHg,TRUE\nKHg11,TRUE\nKHg2,TRUE\nKI,FALSE\nKIO3,FALSE\nKIn(TeO3)2,FALSE\nKInGeS4,FALSE\nKInS2,FALSE\nKInSe2,FALSE\nKInSnS4,FALSE\nKLi(WO3)3,TRUE\nKLiCO3,FALSE\nKLu,TRUE\nKMo6S7,TRUE\nKNa2Sb,FALSE\nKNb2O5,TRUE\nKNb2Se,TRUE\nKNb3(SeO6)2,FALSE\nKNb3(TeO6)2,FALSE\nKNbSe2O7,FALSE\nKP(HO2)2,FALSE\nKPAu5S8,FALSE\nKPPbO4,FALSE\nKPSe3,FALSE\nKPSe6,FALSE\nKRbBi8Se13,FALSE\nKRuO4,TRUE\nKSb,FALSE\nKSb(SO4)2,FALSE\nKSb5S8,FALSE\nKSbS2,FALSE\nKSbSe2,FALSE\nKSc(SeO3)2,FALSE\nKScO3,TRUE\nKSi2P3,FALSE\nKSiBiS4,FALSE\nKSm2CuS4,FALSE\nKSnAuS3,FALSE\nKSnAuSe3,FALSE\nKTa3(TeO6)2,FALSE\nKTa3CuO9,TRUE\nKTaO3,FALSE\nKTbSe4,FALSE\nKTeP2,FALSE\nKThCuS3,FALSE\nKTi2F7,FALSE\nKTi5Se8,TRUE\nKTiPO5,FALSE\nKTm,TRUE\nKUClO3,FALSE\nKUCuSe3,TRUE\nKV2I3O13,FALSE\nKV4Ag11O16,FALSE\nKV6O11,TRUE\nKY(TeO3)2,FALSE\nKYb2F7,TRUE\nKYbSe2,TRUE\nKZn4(BO3)3,FALSE\nKZrPSe6,FALSE\nLa(FeAs3)4,TRUE\nLa(In2Au)2,TRUE\nLa(InS2)3,FALSE\nLa(Ni2B)6,TRUE\nLa(PRu)2,TRUE\nLa(SiOs)2,TRUE\nLa(SiRu)2,TRUE\nLa1.86Tb1.14Ga1.67S7,FALSE\nLa10Mn9O30,TRUE\nLa10Se14O,FALSE\nLa10Si8O3,TRUE\nLa16Mn15O48,TRUE\nLa1Se0.14S1.86,FALSE\nLa2.1Bi5.9Pb2S14,FALSE\nLa20Cu9O40,TRUE\nLa20Mo12Cl4O63,FALSE\nLa2B4Rh5,TRUE\nLa2CuO4,TRUE\nLa2Fe(SeO)2,FALSE\nLa2Fe2I,TRUE\nLa2Ga0.33Sb1S5,FALSE\nLa2Ga2GeS8,FALSE\nLa2Ge2Se7,FALSE\nLa2Ge5Ir3,TRUE\nLa2Ge5Rh3,TRUE\nLa2GeSe5,FALSE\nLa2HfS5,FALSE\nLa2In,TRUE\nLa2Mn(SeO)2,FALSE\nLa2MnNiO6,FALSE\nLa2MoO5,FALSE\nLa2Nb2N2O5,TRUE\nLa2Ni5B4,TRUE\nLa2O3,FALSE\nLa2PC,TRUE\nLa2PI2,TRUE\nLa2PdO4,TRUE\nLa2Pr2O7,TRUE\nLa2Rh7,TRUE\nLa2S3,FALSE\nLa2Se3,FALSE\nLa2Si5Rh3,TRUE\nLa2Sn5Rh3,TRUE\nLa2TiCoO6,FALSE\nLa2V2IO9,FALSE\nLa2VCoO6,FALSE\nLa2VNiO6,FALSE\nLa2YbCuS5,FALSE\nLa2YbCuSe5,FALSE\nLa2Zn(SeO)2,FALSE\nLa2ZrS5,FALSE\nLa3(BN2)2,TRUE\nLa3(OsO5)2,TRUE\nLa3(ReO5)2,TRUE\nLa3AlN,TRUE\nLa3CuGeSe7,FALSE\nLa3Ga1Ge0.5S7,FALSE\nLa3GaCuSe7,FALSE\nLa3Ge3Br2,TRUE\nLa3In1Ge0.5S7,FALSE\nLa3LuSe6,FALSE\nLa3Mg0.5Sn1S14,FALSE\nLa3Mo4O16F,FALSE\nLa3NiBr3,TRUE\nLa3Si1Sb0.33S7,FALSE\nLa3Si1Sb0.33Se7,FALSE\nLa3Te4,FALSE\nLa3ZrSb5,TRUE\nLa4Cd4In2S13,FALSE\nLa4Co3O10,TRUE\nLa4Fe(SbS5)2,FALSE\nLa4Fe(SbSe5)2,FALSE\nLa4In5S13,TRUE\nLa4InSbS9,FALSE\nLa4InSbSe9,FALSE\nLa5Cu6.33S7O4,FALSE\nLa5In3(S3O)3,FALSE\nLa5SmS8,TRUE\nLa5YbS8,TRUE\nLa6Sb4(SO4)3,FALSE\nLa8Mn7O24,TRUE\nLa8Sb2S15,FALSE\nLaAl12O19,TRUE\nLaAl4,TRUE\nLaAl4Co,TRUE\nLaB6,FALSE\nLaBPt3,TRUE\nLaBeB3O7,FALSE\nLaBiAu2,TRUE\nLaCd2,TRUE\nLaCdAg2,TRUE\nLaCdAu,TRUE\nLaCu6,TRUE\nLaCuSO,FALSE\nLaCuSeO,FALSE\nLaCuTeO,FALSE\nLaF3,FALSE\nLaGa,TRUE\nLaGa3Pd2,TRUE\nLaGaO3,FALSE\nLaGaS3,FALSE\nLaGeI,TRUE\nLaH2,TRUE\nLaH2NO5,FALSE\nLaHg,TRUE\nLaIn,TRUE\nLaIn2Ir,TRUE\nLaIn5Ir,TRUE\nLaInS2O,FALSE\nLaMg(FeO3)2,TRUE\nLaMg2H7Pd,FALSE\nLaMg3,TRUE\nLaNbN2O,FALSE\nLaP,FALSE\nLaP3,TRUE\nLaPd3S4,TRUE\nLaPt5,TRUE\nLaRe2Ag,TRUE\nLaReB,TRUE\nLaSb,FALSE\nLaScSi,TRUE\nLaSi,TRUE\nLaSi2,FALSE\nLaSi2Ru,TRUE\nLaSn3Ru,TRUE\nLaTaN2O,FALSE\nLaTb3,TRUE\nLaV,TRUE\nLaVI5O16,FALSE\nLaYbZn2,TRUE\nLaZnAsO,FALSE\nLaZnAu2,TRUE\nLi(CuO)3,TRUE\nLi(NiO2)4,TRUE\nLi0.33Ag1Sn0.67O2,FALSE\nLi0.33Ti0.67Ag1O2,FALSE\nLi0.5Ge1Pb1.75S4,FALSE\nLi11Mn13O32,TRUE\nLi12Fe5O16,TRUE\nLi13Nb14ZnO42,TRUE\nLi13Ti22O48,TRUE\nLi14Ti21O48,TRUE\nLi15(FeO4)4,TRUE\nLi15Mn2O12,TRUE\nLi17Nb20O60,TRUE\nLi17Ti20O40,TRUE\nLi2(FeO2)5,TRUE\nLi2(LuGe)3,TRUE\nLi2(NiO2)3,TRUE\nLi23(MnAs)20,TRUE\nLi2B4O7,FALSE\nLi2CdGe,FALSE\nLi2CdGeS4,FALSE\nLi2CdSnS4,FALSE\nLi2Co4O7F,TRUE\nLi2CrCo3O8,TRUE\nLi2CrCuO4,TRUE\nLi2Cu2S3,TRUE\nLi2CuF6,TRUE\nLi2DyIn,TRUE\nLi2EuSn,TRUE\nLi2Fe2(PO4)3,TRUE\nLi2Fe3CoO8,TRUE\nLi2Fe3NiO8,TRUE\nLi2Fe3SnO8,TRUE\nLi2FeGeS4,FALSE\nLi2FeSnS4,FALSE\nLi2FeWO6,TRUE\nLi2Ga,TRUE\nLi2Ga(GeSe3)2,FALSE\nLi2Ga2GeS6,FALSE\nLi2GaPd,TRUE\nLi2HgGe,FALSE\nLi2HgGeS4,FALSE\nLi2In2GeS6,FALSE\nLi2In2GeSe6,FALSE\nLi2In2SiS6,FALSE\nLi2In2SiSe6,FALSE\nLi2InAg,TRUE\nLi2LaTl,TRUE\nLi2MgHg,TRUE\nLi2MgIn,TRUE\nLi2MgSn,TRUE\nLi2MnCo3O8,TRUE\nLi2MnCu3O8,TRUE\nLi2MnGeS4,FALSE\nLi2MnNi3O8,TRUE\nLi2MnO2F,TRUE\nLi2Mo2Se2O11,FALSE\nLi2Nb2(PO4)3,TRUE\nLi2NdAs2,TRUE\nLi2NdSb2,TRUE\nLi2Ni2SbO6,TRUE\nLi2Ni3TeO8,TRUE\nLi2Ni5(PO4)4,TRUE\nLi2PmAl,TRUE\nLi2PmGe,TRUE\nLi2PrIn,TRUE\nLi2PrP2,TRUE\nLi2PtO3,FALSE\nLi2Si4Ni5O14,TRUE\nLi2SiHgS4,FALSE\nLi2Sn5,TRUE\nLi2SnHgS4,FALSE\nLi2SnIr,TRUE\nLi2TeMoO6,FALSE\nLi2TeWO6,FALSE\nLi2Ti3FeO8,TRUE\nLi2TiMn3O8,TRUE\nLi2TlAg,TRUE\nLi2U(MoO5)2,TRUE\nLi2V2F7,TRUE\nLi2V3CrO8,TRUE\nLi2V3FeO8,TRUE\nLi2YbPb,TRUE\nLi2ZnGe,FALSE\nLi2ZnGeSe4,FALSE\nLi2ZnSnS4,FALSE\nLi2ZnSnSe4,FALSE\nLi3(CoO2)4,TRUE\nLi3(CuO)4,TRUE\nLi3(CuO2)2,TRUE\nLi3AlP2,FALSE\nLi3AlTe4O11,FALSE\nLi3Bi,FALSE\nLi3C,TRUE\nLi3Co(NiO2)4,TRUE\nLi3Co2(GeO4)3,TRUE\nLi3Co3SbO8,TRUE\nLi3Co4TeO8,TRUE\nLi3Cr(NiO2)4,TRUE\nLi3Cr3(CuO6)2,TRUE\nLi3CrCo3O8,TRUE\nLi3CrO4,TRUE\nLi3Cu4NiO8,TRUE\nLi3Dy,TRUE\nLi3Fe(CoO2)4,TRUE\nLi3Fe(SbO3)4,TRUE\nLi3Fe2SbO6,TRUE\nLi3FeNi3O8,TRUE\nLi3FeS3,TRUE\nLi3FeTe4O11,FALSE\nLi3GaTe4O11,FALSE\nLi3Mn(CuO3)2,TRUE\nLi3Mn(NiO3)2,TRUE\nLi3Mn2(CoO4)2,TRUE\nLi3Mn2(PO4)3,TRUE\nLi3Mn2CuO6,TRUE\nLi3Mn3NiO8,TRUE\nLi3Mn3WO8,TRUE\nLi3Mn4(PO4)6,TRUE\nLi3Mn4O8,TRUE\nLi3MnAs2,TRUE\nLi3Mo2P5O18,TRUE\nLi3Ni(SbO3)4,TRUE\nLi3Ni2(GeO4)3,TRUE\nLi3Ni3(PO4)4,TRUE\nLi3PS4,FALSE\nLi3ScN2,FALSE\nLi3Si3Ag2,TRUE\nLi3Ti2(PO4)3,TRUE\nLi3Ti3(PO4)4,TRUE\nLi3V12O29,TRUE\nLi3V4FeO12,TRUE\nLi3V4NiO12,TRUE\nLi3VOF5,TRUE\nLi4(FeO2)9,TRUE\nLi4.5Al0.5Te1O6,FALSE\nLi4.5Cr0.5Te1O6,FALSE\nLi4.5Fe0.5Te1O6,FALSE\nLi4.5Ga0.5Te1O6,FALSE\nLi4.5Mn0.5Te1O6,FALSE\nLi4Co2Ni3O10,TRUE\nLi4Co3CuO8,TRUE\nLi4Co5SbO12,TRUE\nLi4Cr3NiO8,TRUE\nLi4CrO5,TRUE\nLi4Cu(PO4)2,TRUE\nLi4Fe2Cu3O10,TRUE\nLi4Fe3NiO8,TRUE\nLi4Fe7(OF7)2,TRUE\nLi4FeNi3O8,TRUE\nLi4HgGe2S7,FALSE\nLi4MgNi3O8,TRUE\nLi4Mn(WO4)3,TRUE\nLi4Mn3Cr3O12,TRUE\nLi4Mn5Cu3O16,TRUE\nLi4Mn5Nb3O16,TRUE\nLi4Mn5NbO12,TRUE\nLi4Mn5Ni3O16,TRUE\nLi4NbNi3O8,TRUE\nLi4Ni2(PO4)3,TRUE\nLi4Ni3BiO8,TRUE\nLi4Ti5Cr3O16,TRUE\nLi4TiCr3O8,TRUE\nLi4V5Cu3O16,TRUE\nLi4VF7,TRUE\nLi4WO5,TRUE\nLi5(BiO3)4,TRUE\nLi5Co2Ni3O10,TRUE\nLi5Co2O2F5,TRUE\nLi5Cr2Ni5O12,TRUE\nLi5Fe2Ni3O10,TRUE\nLi5Fe6(BO3)6,TRUE\nLi5La3Nb14O42,TRUE\nLi5Mn2Cu5O12,TRUE\nLi5Mn3(FeO5)2,TRUE\nLi5Mn5(SbO6)2,TRUE\nLi5Mn6(BO3)6,TRUE\nLi6(NiO2)5,TRUE\nLi6Fe3Co7O20,TRUE\nLi6Fe9CoO20,TRUE\nLi6FeNi9O20,TRUE\nLi6FeO5F,TRUE\nLi6FeO6,TRUE\nLi6Mn5CoO12,TRUE\nLi6Mn5FeO12,TRUE\nLi6Tb2O7,TRUE\nLi7(Mo3S4)4,TRUE\nLi7(NiO2)11,TRUE\nLi7Ca8Nb12O40,TRUE\nLi7Ti16O32,TRUE\nLi7Ti5O12,TRUE\nLi7Ti7O16,TRUE\nLi8BiS6,TRUE\nLi8GeN4,FALSE\nLi8IrO6,TRUE\nLi8PO3,TRUE\nLi8PrO6,TRUE\nLi8Ti16CuS32,TRUE\nLi8TiNi7O16,TRUE\nLi9Fe3(WO4)7,TRUE\nLi9Ga13(Te7O22)3,FALSE\nLiAgF3,TRUE\nLiAl2Rh,TRUE\nLiAl2Tc,TRUE\nLiAl3,TRUE\nLiAlB14,FALSE\nLiAlB4,TRUE\nLiAlGe,TRUE\nLiAlRh2,TRUE\nLiAsS2,FALSE\nLiAsSe2,FALSE\nLiB3,FALSE\nLiB3O5,FALSE\nLiB9PbO15,FALSE\nLiBePt2,TRUE\nLiBi2(PO4)3,TRUE\nLiBi3(ClO2)2,FALSE\nLiBiS2,FALSE\nLiBr,FALSE\nLiCa2Ga,TRUE\nLiCa2Ge3,TRUE\nLiCa2In,TRUE\nLiCa2Mg,TRUE\nLiCa3As2H,FALSE\nLiCaO3,TRUE\nLiCd2Rh,TRUE\nLiCdBO3,FALSE\nLiCl,FALSE\nLiCo(CO3)2,TRUE\nLiCo7O7F,TRUE\nLiCoS2,TRUE\nLiCu2(CO3)2,TRUE\nLiCu2Ge,TRUE\nLiCu3F7,TRUE\nLiCu5P3O13,TRUE\nLiCuO2,TRUE\nLiCuPO4,TRUE\nLiEr2Ga,TRUE\nLiErAu2,TRUE\nLiEuH3,FALSE\nLiF,FALSE\nLiFe2(PO4)3,TRUE\nLiFe2(SiO4)2,TRUE\nLiGa(GeSe3)2,FALSE\nLiGaAg2,TRUE\nLiGaAu2,TRUE\nLiGaO2,FALSE\nLiGaPd2,TRUE\nLiGaPt2,TRUE\nLiGaS2,FALSE\nLiGaSe2,FALSE\nLiGaTe2,FALSE\nLiGd5P2O13,FALSE\nLiGeRh2,TRUE\nLiH3(SeO3)2,FALSE\nLiHf2Ir,TRUE\nLiHfPd2,TRUE\nLiHg2Pd,TRUE\nLiHoAu2,TRUE\nLiHoO3,TRUE\nLiI,FALSE\nLiIO3,FALSE\nLiIn(IO3)4,FALSE\nLiIn2Rh,TRUE\nLiInAg2,TRUE\nLiInS2,FALSE\nLiInSe2,FALSE\nLiInSn,TRUE\nLiInSnS4,FALSE\nLiInTe2,FALSE\nLiLa2IrO6,TRUE\nLiLu2Ga,TRUE\nLiLu2Pd,TRUE\nLiLu2Ru,TRUE\nLiLu2Tc,TRUE\nLiMg2Ag,TRUE\nLiMgAs,FALSE\nLiMgBi,FALSE\nLiMgN,FALSE\nLiMgSnPd,TRUE\nLiMn(PO4)2,TRUE\nLiMn2(PO4)2,TRUE\nLiMn4O8,TRUE\nLiMn9Se10,TRUE\nLiMnCoO4,TRUE\nLiMnCuO4,TRUE\nLiMnO2,TRUE\nLiMnP2O7,TRUE\nLiMnSiO4,TRUE\nLiMo3O8,TRUE\nLiMoIO6,FALSE\nLiNb3(BiO3)4,FALSE\nLiNbO3,FALSE\nLiNi2(PO4)3,TRUE\nLiNiP2O7,TRUE\nLiPm2Al,TRUE\nLiPm2Ga,TRUE\nLiPm2Ir,TRUE\nLiPm2Si,TRUE\nLiPr2Ru,TRUE\nLiSb3PbS6,FALSE\nLiSbS2,FALSE\nLiSbSe2,FALSE\nLiSbTe2,FALSE\nLiScHg2,TRUE\nLiSiB6,FALSE\nLiSiPd2,TRUE\nLiSiRh2,TRUE\nLiSm3SiS7,FALSE\nLiSn(PO3)4,TRUE\nLiSn4Ir,TRUE\nLiSnAu,TRUE\nLiTa3(BiO3)4,FALSE\nLiTaO3,FALSE\nLiTaRh2,TRUE\nLiThAu2,TRUE\nLiTi11O20,TRUE\nLiTi3O6,TRUE\nLiTiSiO4,TRUE\nLiTlPd2,TRUE\nLiTm2Rh,TRUE\nLiTm2Ru,TRUE\nLiTmSn,TRUE\nLiV2NiO6,TRUE\nLiV3O4,TRUE\nLiY(CuP)2,TRUE\nLiY2Ru,TRUE\nLiYbF4,TRUE\nLiYbPb,TRUE\nLiZn(Fe5O8)2,TRUE\nLiZn2GaO4,FALSE\nLiZnBO3,FALSE\nLiZnN,FALSE\nLiZr2Os,TRUE\nLiZrRh2,TRUE\nLu(InS2)3,FALSE\nLu(SiOs)2,TRUE\nLu2AgAu,TRUE\nLu2Al3Co,TRUE\nLu2AlTc,TRUE\nLu2CdAg,TRUE\nLu2CdIn,TRUE\nLu2CrS4,FALSE\nLu2Fe2Si2C,TRUE\nLu2FeS4,TRUE\nLu2InHg,TRUE\nLu2MgHg,TRUE\nLu2Mn12P7,TRUE\nLu2Mo2C3,TRUE\nLu2O3,FALSE\nLu2TlAg,TRUE\nLu2TlCd,TRUE\nLu2TlCu3Se5,FALSE\nLu3BC3,TRUE\nLu3Ga,TRUE\nLu3InN,TRUE\nLu3TlC,TRUE\nLu4C7,TRUE\nLu5(Si5Ir2)2,TRUE\nLu5Si3B,TRUE\nLu7(NiTe)2,TRUE\nLu7(TePd)2,TRUE\nLuAg2,TRUE\nLuAl2Pd5,TRUE\nLuAlAg2,TRUE\nLuAu,TRUE\nLuBPd3,TRUE\nLuC2,TRUE\nLuCd4B3O10,FALSE\nLuCdAg2,TRUE\nLuGaRh2,TRUE\nLuGe2,TRUE\nLuHfRu2,TRUE\nLuIr,TRUE\nLuIr2,TRUE\nLuMnSi,TRUE\nLuNiBC,TRUE\nLuP,FALSE\nLuPt3,TRUE\nLuScRh2,TRUE\nLuScRu2,TRUE\nLuScZn2,TRUE\nLuSi2Ni,TRUE\nLuSiIr,TRUE\nLuU2S3O2,TRUE\nLuUO3,TRUE\nMg(As2Rh3)2,TRUE\nMg(CoS2)2,TRUE\nMg(FeO2)4,TRUE\nMg(FeS2)2,TRUE\nMg(SnO2)4,TRUE\nMg(TiS2)4,TRUE\nMg10B16Ir19,TRUE\nMg17Al11Pd,TRUE\nMg23Al30,TRUE\nMg2AgIr,TRUE\nMg2Co,FALSE\nMg2CrN2,TRUE\nMg2Cu,TRUE\nMg2CuWO6,TRUE\nMg2Ga,TRUE\nMg2Ge,FALSE\nMg2GeB2Rh5,TRUE\nMg2GeSe4,FALSE\nMg2MnN2,TRUE\nMg2Pb,FALSE\nMg2PdAu,TRUE\nMg2RhAu,TRUE\nMg2Si,FALSE\nMg2SiPt,TRUE\nMg2Sn,FALSE\nMg2TcO4,TRUE\nMg2TiIrO6,TRUE\nMg2V9O13,TRUE\nMg2Zr14O5,TRUE\nMg3(B25C4)2,FALSE\nMg3(MnAl9)2,TRUE\nMg3(Ni10B3)2,TRUE\nMg3(Ni10P3)2,TRUE\nMg32Al36Ag13,TRUE\nMg3Al9FeSi5,TRUE\nMg3As2,FALSE\nMg3AsN,FALSE\nMg3Bi2,TRUE\nMg3Ga7Co2,TRUE\nMg3Ge,TRUE\nMg3N2,FALSE\nMg3P2,FALSE\nMg3Rh,TRUE\nMg3Ru2,TRUE\nMg3Sb2,FALSE\nMg3Tl,TRUE\nMg4Sc3(SiO3)8,TRUE\nMg5As,TRUE\nMg5B3O9F,FALSE\nMg5Ti13O30,TRUE\nMg5Tl2,TRUE\nMg9CuO10,TRUE\nMgAgAs,TRUE\nMgCo2(PO5)2,TRUE\nMgCr,TRUE\nMgCu2GeS4,FALSE\nMgCu2SiS4,FALSE\nMgCuBi,TRUE\nMgCuSb,TRUE\nMgCuSn,TRUE\nMgF2,FALSE\nMgGeN2,FALSE\nMgIn3,TRUE\nMgInAg2,TRUE\nMgInPd2,TRUE\nMgMnO3,TRUE\nMgMnRh2,TRUE\nMgNiSb,TRUE\nMgO,FALSE\nMgPb3,TRUE\nMgPt5,TRUE\nMgRh2Pb,TRUE\nMgRhF6,TRUE\nMgSbF6,TRUE\nMgSbPt,TRUE\nMgSc,TRUE\nMgScAg2,TRUE\nMgSe,FALSE\nMgSi7Ir3,TRUE\nMgSiN2,FALSE\nMgSnRh2,TRUE\nMgTe,FALSE\nMgTi11O20,TRUE\nMgTi4O6,TRUE\nMgTl,TRUE\nMgV4O6,TRUE\nMgZn2,TRUE\nMn(BW)2,TRUE\nMn(CoO2)4,TRUE\nMn(PbO2)2,FALSE\nMn(SbO2)2,FALSE\nMn(SbO3)2,TRUE\nMn(SbSe2)2,FALSE\nMn0.05Te1Pb0.95,FALSE\nMn0.1Te1Pb0.9,FALSE\nMn11Si19,FALSE\nMn15Si26,FALSE\nMn2AlB2,TRUE\nMn2AlO4,TRUE\nMn2CoAs,TRUE\nMn2CoGe,TRUE\nMn2Cu(PO4)3,TRUE\nMn2GaW,TRUE\nMn2GeS4,TRUE\nMn2Hg5,TRUE\nMn2Nb,TRUE\nMn2OF3,TRUE\nMn2P,TRUE\nMn2Tl2O7,TRUE\nMn2VSi,TRUE\nMn3(OF3)2,TRUE\nMn3Al10,TRUE\nMn3Cr3(CoO8)2,TRUE\nMn3Cr3(TeO8)2,TRUE\nMn3NbO8,TRUE\nMn3NiN,TRUE\nMn3PdN,TRUE\nMn3PtN,TRUE\nMn3SbO8,TRUE\nMn3V2(SiO4)3,TRUE\nMn5As4,TRUE\nMn5Ge2,TRUE\nMn5O3F5,TRUE\nMn5O7,TRUE\nMn7O7F,TRUE\nMnAl3,FALSE\nMnAlAu2,TRUE\nMnAs,TRUE\nMnBe2Co,TRUE\nMnCdO2,TRUE\nMnCoSi,TRUE\nMnCu2Sn,TRUE\nMnCu3,TRUE\nMnF2,FALSE\nMnFeAs,TRUE\nMnFeCoGe,TRUE\nMnGaNi2,TRUE\nMnGaPt,TRUE\nMnGePd,TRUE\nMnGeRh2,TRUE\nMnI2,FALSE\nMnIn2PbS5,FALSE\nMnInCu2,TRUE\nMnNbO4,TRUE\nMnNi,TRUE\nMnNiP,TRUE\nMnO,FALSE\nMnO2,FALSE\nMnP2,TRUE\nMnP4,FALSE\nMnPSe3,FALSE\nMnS,TRUE\nMnSb3(PO4)6,TRUE\nMnSbPd,TRUE\nMnSbRh2,TRUE\nMnSe,FALSE\nMnSi,FALSE\nMnSiNi2,TRUE\nMnSnRu2,TRUE\nMnTcOs,TRUE\nMnTe,FALSE\nMnTe9,FALSE\nMnTePd,TRUE\nMnV(TeO4)2,FALSE\nMo2NCl8,TRUE\nMo3Pd2N,TRUE\nMo5As4,TRUE\nMo5O14,TRUE\nMoO3,FALSE\nMoSe2,FALSE\nNa(GeP)3,FALSE\nNa0.5Ge1Pb1.75S4,FALSE\nNa0.5Ge1Pb1.75Se4,FALSE\nNa0.75Eu1.625Ge1Se4,FALSE\nNa0.8Li0.2As1Se2,FALSE\nNa10(Ga2Sn)3,TRUE\nNa11Bi5O16,TRUE\nNa11Ti20O40,TRUE\nNa15Sn4,TRUE\nNa19Zr11S30,TRUE\nNa2B6O9F2,FALSE\nNa2Be4B4O11,FALSE\nNa2Cd(GeS3)2,FALSE\nNa2Cd(GeSe3)2,FALSE\nNa2CdSnS4,FALSE\nNa2Cl,TRUE\nNa2Cr7O14,TRUE\nNa2EuGeSe4,FALSE\nNa2Ga2GeS6,FALSE\nNa2Ga2SnS6,FALSE\nNa2Gd(PO4)2,FALSE\nNa2Ge2Se5,FALSE\nNa2Hg3(GeS4)2,FALSE\nNa2Hg3Se1.49S2.51,FALSE\nNa2In,TRUE\nNa2In2GeS6,FALSE\nNa2In2GeSe6,FALSE\nNa2In2SiS6,FALSE\nNa2In4Se6S,FALSE\nNa2In5Au6,TRUE\nNa2LiTa,TRUE\nNa2Mo2Se2O11,FALSE\nNa2Nb4Se4O19,FALSE\nNa2Pt(IO3)6,FALSE\nNa2S,FALSE\nNa2SO4,TRUE\nNa2Se,FALSE\nNa2Si2Hg3S8,FALSE\nNa2Sn2Hg3S8,FALSE\nNa2Te,FALSE\nNa2TeS3,FALSE\nNa2TeSe3,FALSE\nNa2Ti2Sb2O,TRUE\nNa2Ti3O7,FALSE\nNa2Tl,TRUE\nNa2UI6,TRUE\nNa2V6O13,TRUE\nNa2VCuF7,TRUE\nNa2Zn(GeS3)2,FALSE\nNa2Zn(GeSe3)2,FALSE\nNa2Zn(SnS3)2,FALSE\nNa2Zn3(SeO3)4,FALSE\nNa3(WO3)4,TRUE\nNa3In2Au,TRUE\nNa3Mn2(GeO4)3,TRUE\nNa3MoClO4,FALSE\nNa3MoO4F,FALSE\nNa3Re,TRUE\nNa3Sb,FALSE\nNa3Sn2ClF6,FALSE\nNa3Tl,TRUE\nNa3UF7,TRUE\nNa3WClO4,FALSE\nNa3Zn(BO2)5,FALSE\nNa4Al4Si19,FALSE\nNa4Eu(GeS3)2,FALSE\nNa4Mg(GeSe3)2,FALSE\nNa4Mg(SiSe3)2,FALSE\nNa5Cu7O13,TRUE\nNa5Fe6(SiO3)12,TRUE\nNa5Gd(MoO4)4,FALSE\nNa6CoSe4,TRUE\nNa6FeS4,TRUE\nNa7(CoO3)2,FALSE\nNa7.36Ga7.24Sn4.78Se24,FALSE\nNa8(CuO2)5,TRUE\nNa8Hg3,TRUE\nNa8NbO6,TRUE\nNa8PO3,TRUE\nNa9(WO3)16,TRUE\nNaAlGeS4,FALSE\nNaAsO3,TRUE\nNaAsS2,FALSE\nNaAsSe2,FALSE\nNaB15,FALSE\nNaBi3,TRUE\nNaBiS2,FALSE\nNaBiSe2,FALSE\nNaBr,FALSE\nNaC,TRUE\nNaCd2Au,TRUE\nNaCd4P3,FALSE\nNaCdAsS3,FALSE\nNaCdO3,TRUE\nNaCdSb,TRUE\nNaCeS2,TRUE\nNaCeS3,FALSE\nNaCl,FALSE\nNaCuO,TRUE\nNaEuO2,TRUE\nNaF,FALSE\nNaFe2(SiO3)4,TRUE\nNaFe2O3,TRUE\nNaGaGe3Se8,FALSE\nNaH3(SeO3)2,FALSE\nNaHg,TRUE\nNaI,FALSE\nNaIn(IO3)4,FALSE\nNaIn(TeO3)2,FALSE\nNaIn3S5,FALSE\nNaIn3Se5,FALSE\nNaInS2,FALSE\nNaInSe2,FALSE\nNaInSnS4,FALSE\nNaInTe2,FALSE\nNaIrPb,TRUE\nNaLa2TaO6,FALSE\nNaLaS3,FALSE\nNaLi3,TRUE\nNaLu(Pd3O4)2,TRUE\nNaNO2,FALSE\nNaNb2PS10,FALSE\nNaNbSe2O7,FALSE\nNaNi2O3,TRUE\nNaSb,FALSE\nNaSb(PS3)2,FALSE\nNaSbF6,FALSE\nNaSbS2,FALSE\nNaSbSe2,FALSE\nNaSbTe2,FALSE\nNaSc(SeO3)2,FALSE\nNaSi2Pd3,TRUE\nNaSm(PS3)2,FALSE\nNaSn2,TRUE\nNaTa3,TRUE\nNaTi5Se8,TRUE\nNaTl,TRUE\nNaY(Te2O5)2,FALSE\nNaYb(PS3)2,FALSE\nNaZr2TiF11,TRUE\nNaZrCuTe3,TRUE\nNb(Cl2O)2,TRUE\nNb17Ir3S40,TRUE\nNb2(CoO3)3,TRUE\nNb2AgPS10,FALSE\nNb2Cr4Si5,TRUE\nNb2O5,FALSE\nNb2Pb2Se4O15,FALSE\nNb2Sb,TRUE\nNb2Tl3CuSe12,FALSE\nNb2Tl4S11,FALSE\nNb3(Fe10B3)2,TRUE\nNb3B2,TRUE\nNb3Bi,TRUE\nNb3CuO8,FALSE\nNb3In,TRUE\nNb3IrSe8,TRUE\nNb3Os,TRUE\nNb3Ru,TRUE\nNb3Te,TRUE\nNb3V(PO4)6,TRUE\nNb3VS6,TRUE\nNb40N21O16,TRUE\nNb4Co2PdSe12,TRUE\nNb5Ga4,TRUE\nNb5Ge3,TRUE\nNb5OF14,TRUE\nNb6Co7,TRUE\nNb6VSb3O25,FALSE\nNbAg2(PS4)2,FALSE\nNbCrN,TRUE\nNbCrW,TRUE\nNbCu3Se4,FALSE\nNbCuO3,FALSE\nNbGaCo2,TRUE\nNbHO3,TRUE\nNbHg3F6,TRUE\nNbOsPb,TRUE\nNbPt2,TRUE\nNbRu2Cl,TRUE\nNbSe2,FALSE\nNbSi2,TRUE\nNbSiIr,TRUE\nNbSnIr,FALSE\nNd(Al4Co)2,TRUE\nNd(AsPd)2,TRUE\nNd(CoGe)2,TRUE\nNd(CoSi)2,TRUE\nNd(CrSi)2,TRUE\nNd(GePt)2,TRUE\nNd(InS2)3,FALSE\nNd(NiSn)2,TRUE\nNd(PRu)2,TRUE\nNd(Re2Si)2,TRUE\nNd(SiIr)2,TRUE\nNd1.33Lu0.67S3,FALSE\nNd10Se14O,FALSE\nNd2(SnSe3)3,FALSE\nNd2BC,TRUE\nNd2CdIn,TRUE\nNd2Fe14B,TRUE\nNd2Ge5Rh3,TRUE\nNd2HfS5,FALSE\nNd2IrPd,TRUE\nNd2Ni7P4,TRUE\nNd2O3,FALSE\nNd2Ru2O7,TRUE\nNd2S3,FALSE\nNd2Se3,FALSE\nNd2Te3,FALSE\nNd2WC2,TRUE\nNd2ZnGa,TRUE\nNd2ZrS5,FALSE\nNd3(GeRu)2,TRUE\nNd3AlC,TRUE\nNd3Ge5,TRUE\nNd3In,TRUE\nNd3Ni13B2,TRUE\nNd3Te4,FALSE\nNd3Zr,TRUE\nNd4(GeS4)3,FALSE\nNd4Ge3Rh4,TRUE\nNd4InSbSe9,FALSE\nNd4Mg3Co2,TRUE\nNd4MgRu,TRUE\nNd4O3F7,TRUE\nNd5Ge3,TRUE\nNd5Ge4,TRUE\nNdAgAs2,TRUE\nNdAgPb,TRUE\nNdAl4Ge2Au,TRUE\nNdAl7Au3,TRUE\nNdAs,FALSE\nNdAu3,TRUE\nNdB6,FALSE\nNdBRh3,TRUE\nNdBi,TRUE\nNdCrGe3,TRUE\nNdCu3(RuO3)4,TRUE\nNdCuSO,FALSE\nNdCuTeO,FALSE\nNdErTl2,TRUE\nNdErZn2,TRUE\nNdF3,FALSE\nNdFeSi2,TRUE\nNdGa2Ni,TRUE\nNdGaO3,TRUE\nNdIn3,TRUE\nNdIn5Rh,TRUE\nNdInAu,TRUE\nNdInCu,TRUE\nNdLuSe3,FALSE\nNdMg2,TRUE\nNdMg2Ni9,TRUE\nNdMgNi4,TRUE\nNdMnSbO,TRUE\nNdMoO4F,FALSE\nNdNiC2,TRUE\nNdO2,TRUE\nNdPt,TRUE\nNdRh,TRUE\nNdSb,TRUE\nNdSbPd,TRUE\nNdScGe,TRUE\nNdSmHg2,TRUE\nNdSn2,TRUE\nNdSnRh,TRUE\nNdTe,TRUE\nNdTe2,FALSE\nNdTiGe,TRUE\nNdTlAg2,TRUE\nNdTlPd,TRUE\nNdZn2Ag,TRUE\nNi(CN)2,FALSE\nNi(PO3)4,TRUE\nNi23B6,TRUE\nNi2Ge,TRUE\nNi2Mo3N,TRUE\nNi2Mo4C,TRUE\nNi2Mo4N,TRUE\nNi2PO5,TRUE\nNi2Te3O8,FALSE\nNi3Ge,TRUE\nNi3Pt,TRUE\nNi3S4,TRUE\nNi3SnN,TRUE\nNi4(BiO2)9,TRUE\nNi4(PO4)3,TRUE\nNi7(P2O7)4,TRUE\nNiAgO2,TRUE\nNiAsO3,TRUE\nNiCO4,TRUE\nNiGe,TRUE\nNiGePt2,TRUE\nNiI,TRUE\nNiN,TRUE\nNiO,FALSE\nNiP2,FALSE\nNiS2,FALSE\nNiTe,FALSE\nOsS2,FALSE\nP2H12N7Cl,TRUE\nP2H4RhO9,TRUE\nP2Ir,FALSE\nP2O5,TRUE\nP2Os,FALSE\nP2Pd,FALSE\nP2Pd3S8,FALSE\nP2Pt,FALSE\nP2Rh,FALSE\nP2Ru,FALSE\nP2Se3,FALSE\nP2Se5,FALSE\nP4Os,FALSE\nP4Ru,FALSE\nPH2NO2,TRUE\nPH6NO4,FALSE\nPHPbO3,FALSE\nPOsS,FALSE\nPOsSe,FALSE\nPPdS,FALSE\nPPdSe,FALSE\nPRuS,FALSE\nPSe,FALSE\nPW5O17,TRUE\nPb17(Cl9O4)2,FALSE\nPb1Se0.01S0.99,FALSE\nPb1Se0.5S0.5,FALSE\nPb1Se0.95S0.05,FALSE\nPb1Se0.99S0.01,FALSE\nPb1Se0.9S0.1,FALSE\nPb2O3,FALSE\nPb2SeN2O9,FALSE\nPb3O4,FALSE\nPb3Se2(BrO3)2,FALSE\nPbBr2,FALSE\nPbCl2,FALSE\nPbI2,FALSE\nPbN6,FALSE\nPbO2,FALSE\nPbS,FALSE\nPbSe,FALSE\nPbSeO4,FALSE\nPd(IO3)2,FALSE\nPd16S7,TRUE\nPd2N,TRUE\nPd3(PbS)2,TRUE\nPdO,FALSE\nPdPb2,TRUE\nPdS,FALSE\nPdS2,FALSE\nPdSe,FALSE\nPdSe2,FALSE\nPm2CuGe,TRUE\nPm2IrRh,TRUE\nPm2NiRh,TRUE\nPm2PtAu,TRUE\nPm3I,TRUE\nPmCd3,TRUE\nPmCdPd2,TRUE\nPmDy3,TRUE\nPmGaAu2,TRUE\nPmHgAu2,TRUE\nPmMgAu2,TRUE\nPmMgCd2,TRUE\nPmMgRh2,TRUE\nPmSbRh2,TRUE\nPmSnRh2,TRUE\nPr(BRu)2,TRUE\nPr(BiO3)2,TRUE\nPr(CoAs)2,TRUE\nPr(CoGe)2,TRUE\nPr(FeSi)2,TRUE\nPr(InS2)3,FALSE\nPr(MnSi)2,TRUE\nPr1.29Lu0.71S3,FALSE\nPr10Se14O,FALSE\nPr1Te1.9,FALSE\nPr27Se40,TRUE\nPr2Au,TRUE\nPr2CdSn,TRUE\nPr2Co12P7,TRUE\nPr2Ge2Se7,FALSE\nPr2GeSe5,FALSE\nPr2HgPb,TRUE\nPr2InGe2,TRUE\nPr2InPd2,TRUE\nPr2Ir2O7,TRUE\nPr2S3,FALSE\nPr2Se3,FALSE\nPr2Te3,FALSE\nPr2Te4O11,FALSE\nPr3(Al2Si3)2,TRUE\nPr3Cd,TRUE\nPr3I,TRUE\nPr4InSbSe9,FALSE\nPr4MgRu,TRUE\nPr4Sb3,TRUE\nPr4Te7,FALSE\nPr5In11Ni6,TRUE\nPr5Si4,TRUE\nPr6Fe13Si,TRUE\nPr7Mn8O24,TRUE\nPr9(SbO)5,TRUE\nPrAgAs2,TRUE\nPrAl3Ni2,TRUE\nPrAs,FALSE\nPrAu,TRUE\nPrB4,TRUE\nPrB6,FALSE\nPrBN2,FALSE\nPrBPt4,TRUE\nPrCd,TRUE\nPrCo4B,TRUE\nPrCuSO,FALSE\nPrErIn2,TRUE\nPrErMg2,TRUE\nPrF3,FALSE\nPrFeGe2,TRUE\nPrGaAu2,TRUE\nPrGe3,TRUE\nPrGe5,TRUE\nPrGeAu,TRUE\nPrIn,TRUE\nPrInAu2,TRUE\nPrIr2,TRUE\nPrLuIn2,TRUE\nPrLuSe3,FALSE\nPrMgAg2,TRUE\nPrMgGa,TRUE\nPrMo3,TRUE\nPrMoO4F,FALSE\nPrNiGe2,TRUE\nPrO,FALSE\nPrP,TRUE\nPrSb,FALSE\nPrSbPt,TRUE\nPrSm3,TRUE\nPrSmO2,TRUE\nPrTaN2O,FALSE\nPrTe2,FALSE\nPrTl2InSe4,FALSE\nPrTlSe2,FALSE\nPrTmTl2,TRUE\nPrZn,TRUE\nPt0.97S2,FALSE\nPt3Pb,TRUE\nPt3PbC,TRUE\nPtN,TRUE\nPtS,FALSE\nPtS2,FALSE\nPtSe2,FALSE\nRb1.45Sb7.45Pb3.1Se15,FALSE\nRb1.54Cd1.54Bi2.46S6,FALSE\nRb15Hg16,TRUE\nRb28(Mg3In17)3,TRUE\nRb2AgPS4,FALSE\nRb2BaNb2Se11,FALSE\nRb2Cd(IBr)2,FALSE\nRb2Cd(PSe3)2,FALSE\nRb2Cd3(B4O7)4,FALSE\nRb2Cd3S4,FALSE\nRb2Cd3Se4,FALSE\nRb2Cd3Te4,FALSE\nRb2CrF6,TRUE\nRb2Cu2Sb2S5,FALSE\nRb2Cu2SnS4,FALSE\nRb2FeI4,TRUE\nRb2GeB4O9,FALSE\nRb2Hg(PSe3)2,FALSE\nRb2Hg3(GeS4)2,FALSE\nRb2Mo3Se3O16,FALSE\nRb2Mo9Se10,TRUE\nRb2Na2IrO4,TRUE\nRb2NaNiF6,TRUE\nRb2NaVF6,TRUE\nRb2NbCuS4,FALSE\nRb2NbCuSe4,FALSE\nRb2PS5,FALSE\nRb2Pt(IO3)6,FALSE\nRb2SCl6F,TRUE\nRb2Sn2Hg3S8,FALSE\nRb2Sn3(SbS5)2,FALSE\nRb2Tb3AlF16,TRUE\nRb2Te,FALSE\nRb2TeBr6,FALSE\nRb2TeI6,FALSE\nRb2Ti(AgS2)2,FALSE\nRb2Ti(CuS2)2,FALSE\nRb2VAgS4,FALSE\nRb2VCuS4,FALSE\nRb2Zn3(SeO3)4,FALSE\nRb3(Cu4S3)2,TRUE\nRb3Ag9(PS4)4,FALSE\nRb3Al3Ge7S20,FALSE\nRb3Al3Ge7Se20,FALSE\nRb3Bi2Br9,FALSE\nRb3Bi2I9,FALSE\nRb3Cd(BO2)5,FALSE\nRb3Ga,TRUE\nRb3Li4(BO2)7,FALSE\nRb3Mn,TRUE\nRb3Na(MoO4)2,FALSE\nRb3Nb2AsSe11,FALSE\nRb3Sb,FALSE\nRb3Sb2Br9,FALSE\nRb3Sb2I9,FALSE\nRb3Sm,TRUE\nRb3Ta2AsS11,FALSE\nRb3Tm,TRUE\nRb3Zn(BO2)5,FALSE\nRb4Ag9(SbS3)4,FALSE\nRb4CuSi2O7,TRUE\nRb4Ga4Si19,FALSE\nRb4Ge(PSe3)4,FALSE\nRb4Ge3B6O17,FALSE\nRb4Mo5(PO11)2,FALSE\nRb4Ti3S14,FALSE\nRb5(W4O15)2,TRUE\nRb5(WO3)18,TRUE\nRb5B(SO4)4,FALSE\nRb5Li6(BO2)11,FALSE\nRb5Tl3O,TRUE\nRb6O,TRUE\nRb7Th2(P2Se7)3,FALSE\nRb9Bi13S24,FALSE\nRbAg2SbS4,FALSE\nRbAg2TeS6,FALSE\nRbAg5(PS4)2,FALSE\nRbAgF3,TRUE\nRbB5(H2O3)4,TRUE\nRbBa2(PO3)5,FALSE\nRbBi2,TRUE\nRbBi3Se5,FALSE\nRbBi3TeSe4,FALSE\nRbBiS2,FALSE\nRbBiSe2,FALSE\nRbBr,FALSE\nRbBr3,TRUE\nRbC8,TRUE\nRbCaBO3,FALSE\nRbCd(BO2)3,FALSE\nRbCd13,TRUE\nRbCd4Ga5S12,FALSE\nRbCd4Ga5Se12,FALSE\nRbCd4Ga5Te12,FALSE\nRbCd4In5Se12,FALSE\nRbCl,FALSE\nRbCu(SbS2)2,FALSE\nRbCu2AsS3,FALSE\nRbCu2SbS3,FALSE\nRbCu4AsS4,FALSE\nRbCuPdF5,TRUE\nRbCuSnS3,FALSE\nRbCuSnSe3,FALSE\nRbEuO2,TRUE\nRbF,FALSE\nRbF3,TRUE\nRbGaSnSe4,FALSE\nRbGe3,TRUE\nRbGeB3O7,FALSE\nRbH2(IO3)3,FALSE\nRbH3(SeO3)2,FALSE\nRbHg3,TRUE\nRbHgSbTe3,FALSE\nRbI,FALSE\nRbIn4,TRUE\nRbIn5S6,FALSE\nRbInGeS4,FALSE\nRbInS2,FALSE\nRbInSnS4,FALSE\nRbInTe3O8,FALSE\nRbLiCO3,FALSE\nRbMn4Ga5Te12,FALSE\nRbMn4In5Se12,FALSE\nRbMnTe2,TRUE\nRbMoPO6,FALSE\nRbNa2NiO2,TRUE\nRbNa2Sb,FALSE\nRbNb3(TeO6)2,FALSE\nRbNb4Br11,FALSE\nRbNbSe2O7,FALSE\nRbPPbO4,FALSE\nRbPSe6,FALSE\nRbPdF3,TRUE\nRbSbO3,TRUE\nRbSbS2,FALSE\nRbSbSe2,FALSE\nRbSbTe2,FALSE\nRbSc(SeO3)2,FALSE\nRbTa3(TeO6)2,FALSE\nRbTbSe2,FALSE\nRbTiBr3,TRUE\nRbTmO3,TRUE\nRbU2SbS8,TRUE\nRbUAgS3,TRUE\nRbV(CuS2)2,FALSE\nRbVP2S7,TRUE\nRbWO3,TRUE\nRbY(TeO3)2,FALSE\nRbYbZnSe3,FALSE\nRbZn4In5Se12,FALSE\nRbZrPSe6,FALSE\nRe(TeCl6)2,TRUE\nRe2PbO6,TRUE\nRe2RuBr,TRUE\nRe2W3C,TRUE\nRe3As7,TRUE\nRe3F,TRUE\nRe3P4,TRUE\nRe5(NiAs6)2,TRUE\nReBiO3,TRUE\nReCl4,TRUE\nReF6,TRUE\nReIr3,TRUE\nReO3,FALSE\nReOsRu,TRUE\nRePO5,TRUE\nReS2,FALSE\nReSe2,FALSE\nReSi2,FALSE\nReSn3,TRUE\nRh0.67S2,FALSE\nRh0.67Se2,FALSE\nRh2S3,FALSE\nRh3Pb,TRUE\nRh7(PbO5)3,TRUE\nRhS3,FALSE\nRhSe2,FALSE\nRhSe3,FALSE\nRhSeS,FALSE\nRu3Cl,TRUE\nRuCl3,TRUE\nRuS2,FALSE\nRuSe2,FALSE\nSb2I2F11,TRUE\nSb2O3,FALSE\nSb2Os,FALSE\nSb2PbSe4,FALSE\nSb2Pt,FALSE\nSb2Ru,FALSE\nSb2S3,FALSE\nSb2Se3,FALSE\nSb2Te,TRUE\nSb2Te3,FALSE\nSb2XeF14,TRUE\nSb3IO4,FALSE\nSb4Pb4S11,TRUE\nSb5IO7,FALSE\nSb6Pb4Se13,FALSE\nSb6Pb6Se17,FALSE\nSb8I2O11,FALSE\nSbAs,FALSE\nSbI3,FALSE\nSbOsS,FALSE\nSbOsSe,FALSE\nSbPb2S2I3,FALSE\nSbPbBrO2,FALSE\nSbPbIO2,FALSE\nSbPd3,TRUE\nSbPt3,TRUE\nSbRh3,TRUE\nSbRuSe,FALSE\nSbSBr,FALSE\nSbSI,FALSE\nSbSeBr,FALSE\nSbSeI,FALSE\nSbTeI,FALSE\nSbTeOs,FALSE\nSbTeRh,FALSE\nSbTeRu,FALSE\nSc(CuSe)3,FALSE\nSc(GaFe)6,TRUE\nSc(TiN)9,TRUE\nSc(VGa2)2,TRUE\nSc11(AlGe4)2,TRUE\nSc14Cu14O37,TRUE\nSc2(PO4)3,TRUE\nSc2Al3Ru,TRUE\nSc2CuRu,TRUE\nSc2Fe,FALSE\nSc2FeB2Ir5,TRUE\nSc2GaAg,TRUE\nSc2GaIr,TRUE\nSc2MnC,TRUE\nSc2O3,FALSE\nSc2S3,FALSE\nSc2TlTc,TRUE\nSc3(MnGa3)2,TRUE\nSc3(ReSi2)2,TRUE\nSc3BPb,TRUE\nSc3C4,TRUE\nSc3Fe2Si3,TRUE\nSc3GaC,TRUE\nSc3PbC,TRUE\nSc4Ge6Rh7,TRUE\nSc5Bi3,TRUE\nSc5NCl8,TRUE\nSc5Pb3,TRUE\nSc6FeSb2,TRUE\nSc6NiTe2,TRUE\nSc6Te2Os,TRUE\nSc7CI12,TRUE\nSc8Te3,TRUE\nScAg,TRUE\nScAg(PSe3)2,FALSE\nScAgO2,FALSE\nScAlNi2,TRUE\nScBIr3,TRUE\nScBPd3,TRUE\nScBe5,TRUE\nScCd,FALSE\nScCdAg2,TRUE\nScCdHg2,TRUE\nScCoGe2,TRUE\nScCoO3,TRUE\nScCrO4,TRUE\nScCu2,TRUE\nScCuO2,FALSE\nScGa2,TRUE\nScGe2,TRUE\nScHg,FALSE\nScIr,TRUE\nScN,FALSE\nScNiSb,FALSE\nScPPt,TRUE\nScRh,TRUE\nScRh3C,TRUE\nScSbPd,FALSE\nScSbRh2,TRUE\nScSbRu2,TRUE\nScSi3Ni,TRUE\nScSnPd,TRUE\nScTa2NO5,FALSE\nScTiNbO6,FALSE\nScTiO3,TRUE\nScTlS2,FALSE\nScTlSe2,FALSE\nScTlTe2,FALSE\nScZn2,TRUE\nScZn3,TRUE\nScZnNi2,TRUE\nScZnPt2,TRUE\nSeS,FALSE\nSi(Bi3O5)4,FALSE\nSi0.001Ge0.999,FALSE\nSi0.03Ge0.97,FALSE\nSi0.0645Ge0.9355,FALSE\nSi0.07Ge0.93,FALSE\nSi0.08Ge0.92,FALSE\nSi0.109Ge0.891,FALSE\nSi0.12Ge0.88,FALSE\nSi0.162Ge0.838,FALSE\nSi0.1Ge0.9,FALSE\nSi0.226Ge0.774,FALSE\nSi0.2Ge0.8,FALSE\nSi0.347Ge0.653,FALSE\nSi0.3Ge0.7,FALSE\nSi0.458Ge0.542,FALSE\nSi0.4Ge0.6,FALSE\nSi0.6Ge0.4,FALSE\nSi0.7Ge0.3,FALSE\nSi0.8Ge0.2,FALSE\nSi0.94Ge0.06,FALSE\nSi0.98Ge0.02,FALSE\nSi0.999Ge0.001,FALSE\nSi0.9Ge0.1,FALSE\nSi15(TeP2)4,FALSE\nSi2Ni6B,TRUE\nSi2NiP3,TRUE\nSi2Pd9,TRUE\nSi2Ru,TRUE\nSi2SbO6,TRUE\nSi2Te3,FALSE\nSi3N4,FALSE\nSi3Ru2,FALSE\nSiAs,FALSE\nSiAs2,FALSE\nSiAu3,TRUE\nSiB3,FALSE\nSiBi3O7,TRUE\nSiGe,FALSE\nSiHg3,TRUE\nSiP,FALSE\nSiP2,FALSE\nSiSb,FALSE\nSiSb3,TRUE\nSiSe2,FALSE\nSiSn,FALSE\nSiTe2,FALSE\nSiTe2Os,TRUE\nSiW3,TRUE\nSm(BOs)2,TRUE\nSm(CoSi)2,TRUE\nSm(CuO2)2,TRUE\nSm(CuS)3,FALSE\nSm(CuTe)3,FALSE\nSm(ErSe2)3,FALSE\nSm(InS2)3,FALSE\nSm(MnGe)2,TRUE\nSm(NiSn)2,TRUE\nSm(SiAg)2,TRUE\nSm(SiNi)2,TRUE\nSm1.82Lu2.18Se6,FALSE\nSm2(PPt2)3,TRUE\nSm2(SnSe3)3,FALSE\nSm2AgRu,TRUE\nSm2AlCd,TRUE\nSm2Cu4Sn5,TRUE\nSm2CuAs3O,TRUE\nSm2Fe17,TRUE\nSm2IO2,TRUE\nSm2In,TRUE\nSm2IrPd,TRUE\nSm2Mn3(SbS3)4,FALSE\nSm2Mo2O7,TRUE\nSm2O3,FALSE\nSm2Pd2Pb,TRUE\nSm2RuAu,TRUE\nSm2S3,FALSE\nSm2Sc3,FALSE\nSm2Se3,FALSE\nSm2Te3,FALSE\nSm2Tl,TRUE\nSm2TlHg,TRUE\nSm2TlZn,TRUE\nSm2ZrSe5,FALSE\nSm3(Sb7Te12)2,TRUE\nSm3Al,TRUE\nSm3Al0.33Si1S7,FALSE\nSm3AlN,TRUE\nSm3B(SO)3,FALSE\nSm3OsO7,TRUE\nSm3Sc,TRUE\nSm3Te4,FALSE\nSm3Zr,TRUE\nSm4Al23Ni6,TRUE\nSm4GaSbS9,FALSE\nSm4In21Pd10,TRUE\nSm4InSbS9,FALSE\nSm4MgRh,TRUE\nSm4U4O17,TRUE\nSm5Br11,TRUE\nSm6Br13,TRUE\nSmAg,TRUE\nSmAlCu,TRUE\nSmAs,FALSE\nSmAs2Au,TRUE\nSmAu3,TRUE\nSmB(SbO4)2,FALSE\nSmB6,FALSE\nSmB66,FALSE\nSmBPd3,TRUE\nSmBiW2O9,FALSE\nSmC10,TRUE\nSmCdHg2,TRUE\nSmCo2,TRUE\nSmCo3B2,TRUE\nSmCoC2,TRUE\nSmCrGe3,TRUE\nSmCuO3,TRUE\nSmCuSO,FALSE\nSmCuSe2,FALSE\nSmCuSeO,FALSE\nSmCuSi,TRUE\nSmErMg2,TRUE\nSmHg3,TRUE\nSmHgPd,TRUE\nSmHoHg2,TRUE\nSmHoZn2,TRUE\nSmIn2Rh,TRUE\nSmInAu,TRUE\nSmLuTl2,TRUE\nSmMg3,TRUE\nSmMgHg2,TRUE\nSmNi2B2C,TRUE\nSmNiAs,TRUE\nSmNiC2,TRUE\nSmP,FALSE\nSmPbAu,TRUE\nSmS,FALSE\nSmSb,FALSE\nSmSb2,TRUE\nSmSe,FALSE\nSmSi3Pt5,TRUE\nSmSnPd,TRUE\nSmSnRh2,TRUE\nSmSnTe2,FALSE\nSmTe,FALSE\nSmTh3,TRUE\nSmTmZn2,TRUE\nSn(PO3)3,TRUE\nSn0.001Pb0.999Se1,FALSE\nSn0.001Te1Pb0.999,FALSE\nSn0.01Pb0.99Se1,FALSE\nSn0.01Te1Pb0.99,FALSE\nSn0.03Pb0.97Se1,FALSE\nSn0.03Te1Pb0.97,FALSE\nSn0.05Pb0.95Se1,FALSE\nSn0.06Pb0.94Se1,FALSE\nSn0.06Te1Pb0.94,FALSE\nSn0.07Pb0.93Se1,FALSE\nSn0.08Pb0.92Se1,FALSE\nSn0.08Te0.08Pb0.92Se0.92,FALSE\nSn0.08Te1Pb0.92,FALSE\nSn0.13Pb0.87Se1,FALSE\nSn0.15Pb0.85Se1,FALSE\nSn0.15Te0.15Pb0.85Se0.85,FALSE\nSn0.15Te1Pb0.85,FALSE\nSn0.17Pb0.83Se1,FALSE\nSn0.17Te1Pb0.83,FALSE\nSn0.1Pb0.9Se1,FALSE\nSn0.1Te1Pb0.9,FALSE\nSn0.23Te1Pb0.77,FALSE\nSn0.25Pb0.75Se1,FALSE\nSn0.25Te1Pb0.75,FALSE\nSn0.28Te0.28Pb0.72Se0.72,FALSE\nSn0.2Pb0.8Se1,FALSE\nSn0.2Te0.2Pb0.8Se0.8,FALSE\nSn0.2Te1Pb0.8,FALSE\nSn0.35Te0.35Pb0.65Se0.65,FALSE\nSn0.99Te1Pb0.01,FALSE\nSn1Se0.01S0.99,FALSE\nSn1Se0.2S0.8,FALSE\nSn1Se0.6S0.4,FALSE\nSn1Se0.75S0.25,FALSE\nSn1Se0.99S0.01,FALSE\nSn2BiS2I3,FALSE\nSn2BiSI5,FALSE\nSn2S,FALSE\nSn2SbS2I3,FALSE\nSn2WO5,FALSE\nSn3As2,FALSE\nSn3Ir2Se3,FALSE\nSn3P3O13,TRUE\nSn3Pd,TRUE\nSn3WO6,FALSE\nSn5(BIr3)2,TRUE\nSn5(BRh3)2,TRUE\nSnAs3,TRUE\nSnB,TRUE\nSnBr2,FALSE\nSnCl2,FALSE\nSnGe,FALSE\nSnGeS3,FALSE\nSnHgO3,FALSE\nSnI2,FALSE\nSnI4,FALSE\nSnO,FALSE\nSnO2,FALSE\nSnPbS3,FALSE\nSnPt3C,TRUE\nSnRh,TRUE\nSnS,FALSE\nSnS2,FALSE\nSnSb3(PO4)4,TRUE\nSnSe,FALSE\nSnSe2,FALSE\nSnTe,FALSE\nSr(CeS2)2,TRUE\nSr(CeSe2)2,TRUE\nSr(CoP)2,TRUE\nSr(GaAu)2,TRUE\nSr(In4Rh)2,TRUE\nSr(LaS2)2,FALSE\nSr(NdS2)2,FALSE\nSr(PrS2)2,FALSE\nSr(RuO3)2,TRUE\nSr(Sb3Ru)4,TRUE\nSr(YbS2)2,TRUE\nSr0.5Ta1O3,FALSE\nSr10Al4Si6O,TRUE\nSr2Be2B2O7,FALSE\nSr2Co2O5,TRUE\nSr2CoReO6,TRUE\nSr2Cu(ClO)2,TRUE\nSr2GaCo2O7,TRUE\nSr2GeN2,TRUE\nSr2HoRuO6,TRUE\nSr2La2.58Bi5.42S14,FALSE\nSr2La2Pt1O7.13,FALSE\nSr2Li2Nb3O10,TRUE\nSr2MgIrO6,TRUE\nSr2MgReO6,TRUE\nSr2Pr2Pt1O7.07,FALSE\nSr2ScSbO6,FALSE\nSr2SmTaO6,FALSE\nSr2TiO4,FALSE\nSr2V2(SeO5)3,FALSE\nSr2V3Se5O18,FALSE\nSr2YBi2O7,TRUE\nSr2YReO6,TRUE\nSr2ZnReO6,TRUE\nSr3(AlSn)2,TRUE\nSr3(SnIr)4,TRUE\nSr3Bi(PO4)3,FALSE\nSr3Co2S2O5,TRUE\nSr3Eu(PO4)3,FALSE\nSr3Ge(SbSe4)2,FALSE\nSr3Li4La5O12,TRUE\nSr3Sb2,TRUE\nSr3ScNiO6,TRUE\nSr3Se3ClO8,FALSE\nSr3Ti2O7,FALSE\nSr4Ga8Ge15,FALSE\nSr4Te3(ClO2)4,FALSE\nSr4V2(Se2O7)3,FALSE\nSr5Bi3,TRUE\nSr5Cd2Sb5F,TRUE\nSr5Sn3,TRUE\nSr5V3O12F,FALSE\nSr6Nb7O21,TRUE\nSr7Bi23O40,TRUE\nSr8(MnN3)3,TRUE\nSr8.007Ge2.043Bi7.949Se24,FALSE\nSr8Al7,TRUE\nSr8Co8O23,TRUE\nSr8Fe3N8,TRUE\nSrAg,TRUE\nSrAl,TRUE\nSrB2,TRUE\nSrB6,FALSE\nSrBiClO2,FALSE\nSrCd,TRUE\nSrCdSi,TRUE\nSrCrO4,FALSE\nSrCuBi,TRUE\nSrGe2,FALSE\nSrIn2,TRUE\nSrIn2(GeIr)4,FALSE\nSrIn2Ir,TRUE\nSrIn2Rh,TRUE\nSrIn4Ir,TRUE\nSrIn4Pt,TRUE\nSrLa3MnO8,TRUE\nSrLaMn2O6,TRUE\nSrLi2Sn,TRUE\nSrLi4(BO3)2,FALSE\nSrMgIn3,TRUE\nSrMgSnSe4,FALSE\nSrMnGe,TRUE\nSrN2,TRUE\nSrNi2(PO4)2,TRUE\nSrNi5As3,TRUE\nSrO,FALSE\nSrPb3,TRUE\nSrPb3Br8,FALSE\nSrPbO3,FALSE\nSrRhF6,TRUE\nSrS,FALSE\nSrSbAu,TRUE\nSrSe,FALSE\nSrSeO4,FALSE\nSrSiPd,TRUE\nSrSnO3,FALSE\nSrSnP,TRUE\nSrTaNO2,FALSE\nSrTe,FALSE\nSrTh(PS4)2,FALSE\nSrTiO3,FALSE\nSrTl2,TRUE\nSrTlHg2,TRUE\nSrUS2,TRUE\nSrV13O18,TRUE\nSrZnSO,FALSE\nSrZnSb2,TRUE\nSrZr2Nb,TRUE\nSrZrS3,FALSE\nTa11(CuO15)2,FALSE\nTa11(CuO6)5,FALSE\nTa22(CuS12)3,TRUE\nTa2Mn3O8,FALSE\nTa2MoOs,TRUE\nTa2N,TRUE\nTa2Nb3O12,TRUE\nTa2O5,FALSE\nTa2OsW,TRUE\nTa2PtSe7,TRUE\nTa2TiN3,TRUE\nTa2Tl4S11,FALSE\nTa2TlO6,TRUE\nTa3B4,TRUE\nTa3P,TRUE\nTa4AlC3,TRUE\nTa4Cu2O11,FALSE\nTa4FeTe4,TRUE\nTa4N5,TRUE\nTa5N6,TRUE\nTa6Be15Cu8,TRUE\nTa6Ni16Ge7,TRUE\nTa7Cu3O19,FALSE\nTaAl3,TRUE\nTaAlPt,TRUE\nTaAs,TRUE\nTaBe2,TRUE\nTaCoSn2,TRUE\nTaCu3S4,FALSE\nTaF3,TRUE\nTaGaPt,TRUE\nTaGaS2,FALSE\nTaGaSe2,FALSE\nTaInNi,TRUE\nTaN,FALSE\nTaNO,FALSE\nTaNiB2,TRUE\nTaPd3,TRUE\nTaPt3,TRUE\nTaRh3,TRUE\nTaTiFe2,TRUE\nTaTl3S4,FALSE\nTaTlS3,FALSE\nTaW3,TRUE\nTb(Al2Fe)4,TRUE\nTb(AlC)3,TRUE\nTb(CoB)2,TRUE\nTb(CoGe)2,TRUE\nTb(CuSe)3,FALSE\nTb(CuTe)3,FALSE\nTb(FeP3)4,TRUE\nTb(GePd)2,TRUE\nTb(GeRh)2,TRUE\nTb(InS2)3,FALSE\nTb(MnGe)6,TRUE\nTb(Ni2P)2,TRUE\nTb0.52Pr2.48Ga1.67S7,FALSE\nTb10B7C10,TRUE\nTb11S16,TRUE\nTb2(MoO4)3,FALSE\nTb2AlCo2,TRUE\nTb2C3,TRUE\nTb2EuSe4,FALSE\nTb2GeS5,FALSE\nTb2In16Pt7,TRUE\nTb2O3,FALSE\nTb2Sb5,TRUE\nTb2SbO2,TRUE\nTb2Ti3Ge4,TRUE\nTb3(MnC3)2,TRUE\nTb3FeB7,TRUE\nTb3Ge5,TRUE\nTb3Ni13B2,TRUE\nTb3ReO7,TRUE\nTb3Si,TRUE\nTb4Al2O9,FALSE\nTb4GaSbS9,FALSE\nTb5Ti5O17,TRUE\nTb5Tl3,TRUE\nTb6PbSe10,TRUE\nTbB(SbO4)2,FALSE\nTbBRh3,TRUE\nTbBe13,TRUE\nTbCl,TRUE\nTbCo2,TRUE\nTbCu5,TRUE\nTbGa,TRUE\nTbGa2Co3,TRUE\nTbGa3,TRUE\nTbH2,TRUE\nTbHg2,TRUE\nTbIn2Ni,TRUE\nTbInAg2,TRUE\nTbInIr,TRUE\nTbMn5Ge3,TRUE\nTbNi5,TRUE\nTbNiGe2,TRUE\nTbNiO3,TRUE\nTbP,TRUE\nTbPt,TRUE\nTbRh2,TRUE\nTbSb2,TRUE\nTbSe2,TRUE\nTbSnAu,TRUE\nTbTe,TRUE\nTbTl,TRUE\nTbWClO4,FALSE\nTbYHg2,TRUE\nTbYbHg2,TRUE\nTbYbRh2,TRUE\nTbZn2,TRUE\nTbZrSb,TRUE\nTc3Pd,TRUE\nTcB,TRUE\nTcS2,FALSE\nTcSe2,FALSE\nTe0.01Pb1Se0.99,FALSE\nTe0.05Pb1Se0.95,FALSE\nTe0.4Se0.6,FALSE\nTe0.5Pb1Se0.5,FALSE\nTe0.5Se0.5,FALSE\nTe0.6Se0.4,FALSE\nTe0.8Se0.2,FALSE\nTe0.99Pb1Se0.01,FALSE\nTe2Au,TRUE\nTe2Mo,FALSE\nTe2Mo(WS2)3,TRUE\nTe2Mo2WSe4,TRUE\nTe2Mo3Se4,TRUE\nTe2MoWS2,TRUE\nTe2Os,FALSE\nTe2Pd,FALSE\nTe2Pd3,TRUE\nTe2Pd3Pb2,TRUE\nTe2Ru,FALSE\nTe2W2SeS,TRUE\nTe3As2,FALSE\nTe3MoWS,TRUE\nTe4Mo(WS)2,TRUE\nTe4MoW3S4,TRUE\nTeAs,FALSE\nTeI,FALSE\nTeI4,FALSE\nTeMoSe,TRUE\nTeO2,FALSE\nTePb,FALSE\nTePb3Cl4O3,FALSE\nTePd,TRUE\nTeSe,FALSE\nTeSe3,FALSE\nTeWCl9,TRUE\nTh(Al2Fe)4,TRUE\nTh(Al5Fe)2,TRUE\nTh(FeGe)2,TRUE\nTh(FeSi)2,TRUE\nTh(GePd)2,TRUE\nTh(MnGe)2,TRUE\nTh(SiRu)2,TRUE\nTh2CrN3,TRUE\nTh2Fe7,TRUE\nTh2GeSe2,FALSE\nTh2In,TRUE\nTh2Se5,FALSE\nTh3B2C3,TRUE\nTh6Mg23,TRUE\nThAl,TRUE\nThAl3,TRUE\nThAsSe,TRUE\nThBi2,TRUE\nThCrB4,TRUE\nThFe2SiC,TRUE\nThHg2,TRUE\nThIr5,TRUE\nThMn4(CuO4)3,TRUE\nThO2,FALSE\nThPSe,TRUE\nThPd3,TRUE\nThRh2,TRUE\nThRu3C,TRUE\nThS,TRUE\nThSO,FALSE\nThSeO,FALSE\nThSi,TRUE\nThSi2Ru3,TRUE\nThTeO,FALSE\nThU8O18,TRUE\nTi(Bi3O5)4,FALSE\nTi10O11,TRUE\nTi11O18,TRUE\nTi13S24,TRUE\nTi1C0.9,FALSE\nTi20(Sb3Se)3,TRUE\nTi2AlV,TRUE\nTi2B,TRUE\nTi2BRh6,TRUE\nTi2Be17,TRUE\nTi2C,TRUE\nTi2Cd,TRUE\nTi2CoGe,TRUE\nTi2CoS4,TRUE\nTi2CuS4,TRUE\nTi2MnFe,TRUE\nTi2NiH,TRUE\nTi2NiSe4,TRUE\nTi2OsRu,TRUE\nTi2RePd,TRUE\nTi2ReRh,TRUE\nTi2ReRu,TRUE\nTi2Sb(PO4)3,TRUE\nTi2TcNi,TRUE\nTi2TcPd,TRUE\nTi2ZnS4,TRUE\nTi3Be,TRUE\nTi3Cu3O,TRUE\nTi3Fe3O,TRUE\nTi3PO7,TRUE\nTi3Pt5,TRUE\nTi3SnC2,TRUE\nTi4NiBi2,TRUE\nTi4O5,TRUE\nTi4ZnO8,TRUE\nTi5(B6O13)2,TRUE\nTi5Zn4(TeO6)3,TRUE\nTi5ZnO7,TRUE\nTi6H2O13,FALSE\nTi9O10,TRUE\nTi9O8,TRUE\nTiAl,TRUE\nTiAlAu2,TRUE\nTiAsRh,TRUE\nTiAuCl,TRUE\nTiBi25O39,FALSE\nTiBr2,TRUE\nTiC,TRUE\nTiCoGe,TRUE\nTiCoSb,FALSE\nTiCoSn,TRUE\nTiCr3(PO4)6,TRUE\nTiFe2,TRUE\nTiFe2As,TRUE\nTiFe2Sb,TRUE\nTiFe2Si,FALSE\nTiFeH2,TRUE\nTiGaIr2,TRUE\nTiHgO3,TRUE\nTiI,TRUE\nTiMn2Al,TRUE\nTiMn2Ge,TRUE\nTiNiSb,FALSE\nTiO2,FALSE\nTiOs3,TRUE\nTiPO4,TRUE\nTiPd,TRUE\nTiReN3,TRUE\nTiS2,FALSE\nTiS3,FALSE\nTiSe,TRUE\nTiSe2,FALSE\nTiTc2Sb,TRUE\nTiTe2,FALSE\nTiTlPS5,FALSE\nTiTlS2,FALSE\nTiTlSe2,FALSE\nTiV4CuO12,TRUE\nTiZn3,TRUE\nTl(Cu3S2)2,TRUE\nTl(MoSe)3,TRUE\nTl(WO3)3,TRUE\nTl0.001Te1Pb0.999,FALSE\nTl0.005Te1Pb0.995,FALSE\nTl0.01Te1Pb0.99,FALSE\nTl0.04Te1Pb0.96,FALSE\nTl0.07Te1Pb0.93,FALSE\nTl16O15F17,TRUE\nTl2.35Sb8.65Se14,FALSE\nTl2BiP2S7,FALSE\nTl2CdTe4,TRUE\nTl2Cu2SnS4,FALSE\nTl2GeTe3,FALSE\nTl2Hg3S4,FALSE\nTl2Hg3Se4,FALSE\nTl2Hg3Te4,FALSE\nTl2InGaSe4,FALSE\nTl2InGaTe4,FALSE\nTl2Mo7O22,TRUE\nTl2O3,FALSE\nTl2PAuS4,FALSE\nTl2S,FALSE\nTl2Se,FALSE\nTl2Te3,FALSE\nTl2Te3As2Se,FALSE\nTl2TeBr6,FALSE\nTl2TeI6,FALSE\nTl2TeS3,FALSE\nTl3AsSe3,FALSE\nTl3Cr,TRUE\nTl3Ir,TRUE\nTl3Pb,TRUE\nTl3Si,TRUE\nTl3VS4,FALSE\nTl4CdI6,FALSE\nTl4CuTeO6,FALSE\nTl4In3GaS8,FALSE\nTl5Te3,TRUE\nTl6Cu(TeO5)2,FALSE\nTl8Os8O27,TRUE\nTl9SbSe6,TRUE\nTlAgSe2,FALSE\nTlAgTe2,FALSE\nTlAsS2,FALSE\nTlAsSe2,FALSE\nTlBiTe2,FALSE\nTlBiTe3,FALSE\nTlBr,FALSE\nTlCdS2,FALSE\nTlCl,FALSE\nTlCoBi,TRUE\nTlCoMo2,TRUE\nTlCr5(Se3S)2,FALSE\nTlCr5(SeS)4,FALSE\nTlCr5(SeS3)2,FALSE\nTlCr5S8,FALSE\nTlCr5Se3S5,FALSE\nTlCr5Se5S3,FALSE\nTlCr5Se7S,FALSE\nTlCr5Se8,FALSE\nTlCr5SeS7,FALSE\nTlCuCl3,FALSE\nTlCuSe2,FALSE\nTlFeI3,TRUE\nTlGaS2,FALSE\nTlGaSe2,FALSE\nTlGaTe2,FALSE\nTlHg6S4Br5,FALSE\nTlHg6Se4Br5,FALSE\nTlInGeS4,FALSE\nTlInHgS3,FALSE\nTlInS2,FALSE\nTlInSe2,FALSE\nTlInTe2,FALSE\nTlN,FALSE\nTlN3,FALSE\nTlNi,TRUE\nTlPS2,FALSE\nTlPSe2,FALSE\nTlS,FALSE\nTlS2,FALSE\nTlSbS2,FALSE\nTlSbSe2,FALSE\nTlSbTe3,FALSE\nTlSe,FALSE\nTlSn,TRUE\nTlSnAuSe3,FALSE\nTlTe,TRUE\nTlTeP,FALSE\nTlZn2Tc,TRUE\nTm(CoSi)2,TRUE\nTm(CuGe)2,TRUE\nTm(CuS)2,TRUE\nTm(CuTe)3,FALSE\nTm(FeSi)2,TRUE\nTm(GeRu)2,TRUE\nTm(MnGe)6,TRUE\nTm(NiGe)2,TRUE\nTm(SiOs)2,TRUE\nTm2AlOs,TRUE\nTm2CdHg,TRUE\nTm2CuTc,TRUE\nTm2Ga10Os3,TRUE\nTm2In,TRUE\nTm2IrPd,TRUE\nTm2MgRu,TRUE\nTm2MgTl,TRUE\nTm2O3,FALSE\nTm2Ru2O7,TRUE\nTm2ZnAg,TRUE\nTm2ZnGa,TRUE\nTm2ZnHg,TRUE\nTm2ZnOs,TRUE\nTm3(GePd)4,TRUE\nTm3GaC,TRUE\nTm4In(NiGe2)2,TRUE\nTm4Sb2Se11.68,FALSE\nTm5(Ge5Rh2)2,TRUE\nTm5Ti5O17,TRUE\nTmAl4Ni,TRUE\nTmAlCu,TRUE\nTmAs,FALSE\nTmAu,TRUE\nTmAu2,TRUE\nTmB2C,TRUE\nTmBPd3,TRUE\nTmBRh3,TRUE\nTmCdAg2,TRUE\nTmCoSi2,TRUE\nTmCu4Ag,TRUE\nTmCuSi,TRUE\nTmGe,TRUE\nTmH2,TRUE\nTmIn3,TRUE\nTmLuPd2,TRUE\nTmMg2Sc,TRUE\nTmMgAg2,TRUE\nTmMgCd2,TRUE\nTmMnGe,TRUE\nTmMnO3,TRUE\nTmPd,TRUE\nTmSb,TRUE\nTmScHg2,TRUE\nTmSnRh,TRUE\nTmSnRu2,TRUE\nTmThRu2,TRUE\nTmTl,TRUE\nTmU2S3O2,TRUE\nU(Al2Fe)4,TRUE\nU(BH4)4,TRUE\nU(CoGe)2,TRUE\nU(CrC)4,TRUE\nU(CuP)2,TRUE\nU(MnSi)2,TRUE\nU(SiNi)2,TRUE\nU11O5,TRUE\nU2(Co7B2)3,TRUE\nU2Al3C4,TRUE\nU2AlCo2,TRUE\nU2AlCo3,TRUE\nU2Cl5O2,TRUE\nU2Cr30P19,TRUE\nU2Cu2As3O,TRUE\nU2MnN3,TRUE\nU2Re2C3,TRUE\nU2SnRh2,TRUE\nU2TeN2,TRUE\nU2Ti,TRUE\nU2Zn17,TRUE\nU3Bi4,TRUE\nU3Cu2Se7,TRUE\nU3Nb,TRUE\nU3Ni3Sn4,TRUE\nU3Se4,TRUE\nU4N7,TRUE\nU4Re7Si6,TRUE\nU4S3,TRUE\nU5Ge3,TRUE\nU6Co,TRUE\nUAl3,TRUE\nUAl4,TRUE\nUAlNi4,TRUE\nUAu2,TRUE\nUCo4Sn,TRUE\nUCoSi,TRUE\nUCuP2,TRUE\nUFe5Si3,TRUE\nUFeSi,TRUE\nUGa2,TRUE\nUGa3Ni,TRUE\nUGa5Ir,TRUE\nUGaNi,TRUE\nUGeRh,TRUE\nUHg3(TeCl3)2,FALSE\nUHg4(AsCl3)2,FALSE\nUNiSn,TRUE\nUO,FALSE\nUO2,FALSE\nUP2S7,FALSE\nUP2S9,FALSE\nUPt3,TRUE\nUSbSe,TRUE\nUSeS,TRUE\nUSi3,TRUE\nUVC2,TRUE\nV12P7,TRUE\nV2(OF)3,TRUE\nV2Bi4O11,FALSE\nV2Cd2Te2O11,FALSE\nV2GaSn2,TRUE\nV2NO,TRUE\nV2O5,FALSE\nV2OsRu,TRUE\nV2Pb4(Se2O7)3,FALSE\nV2Sb(PO4)3,TRUE\nV2Si2O7,TRUE\nV2TcRu,TRUE\nV2Zn3TeO10,FALSE\nV2ZnO4,TRUE\nV3(HO2)4,TRUE\nV3Ag,TRUE\nV3As2O9,FALSE\nV3Bi(PbO4)3,FALSE\nV3Cd4(TeO5)3,FALSE\nV3CrO10,TRUE\nV3Cu,TRUE\nV3CuO8,TRUE\nV3Pb2Se5O18,FALSE\nV3Pt,TRUE\nV3Re,TRUE\nV3Si,TRUE\nV3SiNi2,TRUE\nV4ZnO8,TRUE\nV5SiB2,TRUE\nV6AgO15,TRUE\nV6PbO11,TRUE\nV8O,TRUE\nVAg(IO4)2,FALSE\nVAg(PSe3)2,TRUE\nVAg2I3O11,FALSE\nVB2,TRUE\nVBi(SeO4)2,FALSE\nVBi24O41,FALSE\nVCo,TRUE\nVCu3(PO4)4,TRUE\nVCu3S4,FALSE\nVFeRu2,TRUE\nVFeSb,FALSE\nVGa(TeO4)2,FALSE\nVIn(NiO3)2,FALSE\nVIr,TRUE\nVIr3,TRUE\nVNi2,TRUE\nVNi5(PO4)6,TRUE\nVO,FALSE\nVO2,FALSE\nVP,TRUE\nVP4,TRUE\nVPO4,TRUE\nVPt2,TRUE\nVSb,TRUE\nVTc,TRUE\nVTe2,TRUE\nVTeHO5,FALSE\nVZn2BiO6,FALSE\nVZnRu2,TRUE\nW2C,TRUE\nW2N,TRUE\nW3O7F,TRUE\nWCl3,TRUE\nWO3,FALSE\nWSe2,FALSE\nY(Al2Cu)4,TRUE\nY(Al5Fe)2,TRUE\nY(AlSi)2,TRUE\nY(CrSi)2,TRUE\nY(CuSe)3,FALSE\nY(CuSi)2,TRUE\nY(CuTe)3,FALSE\nY(FeSi)2,TRUE\nY(NiP)2,TRUE\nY(Re2Si)2,TRUE\nY(SiPt)2,TRUE\nY(SiRh)2,TRUE\nY(SiRu)2,TRUE\nY(TiGa2)2,TRUE\nY2AlZn,TRUE\nY2C3,TRUE\nY2CuO4,TRUE\nY2Fe2Si2C,TRUE\nY2Ge2O7,TRUE\nY2Ge5Ir3,TRUE\nY2Mo2O7,TRUE\nY2O3,FALSE\nY2ReB6,TRUE\nY2Ru2O7,TRUE\nY2S3,FALSE\nY2U3O11,TRUE\nY3(Fe31B7)2,TRUE\nY3Al3NiGe2,TRUE\nY3Fe29,TRUE\nY3GaCo3,TRUE\nY3GaS6,FALSE\nY3Ge4,TRUE\nY3Si3Pd2,TRUE\nY3Tm,TRUE\nY4AsSe3,TRUE\nY4C7,TRUE\nY4CuTe8,TRUE\nY4GaSbS9,FALSE\nY4US5O3,FALSE\nY6Zn(SiS7)2,FALSE\nYAgO3,TRUE\nYAlGe,TRUE\nYAlPd,TRUE\nYAs,TRUE\nYB2C,TRUE\nYB2Rh2C,TRUE\nYB66,FALSE\nYBi,TRUE\nYCd4B3O10,FALSE\nYCdHg2,TRUE\nYCdPd2,TRUE\nYCdPt2,TRUE\nYCo2,TRUE\nYCoO3,TRUE\nYCu3(WO3)4,TRUE\nYCuO2,FALSE\nYErRh2,TRUE\nYH2,TRUE\nYH2NO5,FALSE\nYHg2,TRUE\nYIn2Ni,TRUE\nYMg4Cu,TRUE\nYMgAl,TRUE\nYMgCu4,TRUE\nYMgGa,TRUE\nYMoClO4,FALSE\nYMoO4F,FALSE\nYN,FALSE\nYNi4B,TRUE\nYNiSb,FALSE\nYSbPd,FALSE\nYSbPt,FALSE\nYScO2,TRUE\nYSi2,TRUE\nYSiNi,TRUE\nYSiRu,TRUE\nYSn3,TRUE\nYTi4(CuO4)3,TRUE\nYTiO3,TRUE\nYTmCu2,TRUE\nYV(BiO4)2,FALSE\nYVSeO10,FALSE\nYVTeO10,FALSE\nYWO3,TRUE\nYZn5,TRUE\nYZnBiO4,FALSE\nYb(Al2Mo)2,TRUE\nYb(AlGa)2,TRUE\nYb(AlGe)2,TRUE\nYb(AlSi)2,TRUE\nYb(CuS)3,FALSE\nYb(CuSe)3,FALSE\nYb(Fe2Ge)2,TRUE\nYb(Ga4Co)2,TRUE\nYb(GaS2)2,FALSE\nYb(GaSe2)2,FALSE\nYb(HO)3,TRUE\nYb(IO3)3,TRUE\nYb(InS2)3,FALSE\nYb(MnAs)2,TRUE\nYb(SbS2)2,FALSE\nYb(SbTe2)2,FALSE\nYb(SiAg)2,TRUE\nYb(SiRh)2,TRUE\nYb11(Ni10C)6,TRUE\nYb14Ti10O41,TRUE\nYb16S29,TRUE\nYb2(ZnGe)3,TRUE\nYb23Mg4Cu7,TRUE\nYb2Ce8O19,TRUE\nYb2EuS4,FALSE\nYb2EuSe4,FALSE\nYb2Ge2Ir,TRUE\nYb2HgPb,TRUE\nYb2InPd2,TRUE\nYb2MgS4,TRUE\nYb2MgSe4,TRUE\nYb2O3,FALSE\nYb2SmS4,TRUE\nYb2Sn,TRUE\nYb2ZnPb,TRUE\nYb3Al5O12,TRUE\nYb3Sn13Rh4,TRUE\nYb3Tc,TRUE\nYb3Ti3O14,TRUE\nYb3V,TRUE\nYb4Sb2S11.25,FALSE\nYb4Sb3,TRUE\nYb5Au4,TRUE\nYb6U3O17,TRUE\nYb8Ge3Sb5,TRUE\nYbAg2,TRUE\nYbAgGe,TRUE\nYbAgO2,TRUE\nYbAl3,TRUE\nYbAs,FALSE\nYbB2Rh3,TRUE\nYbB66,FALSE\nYbBO3,TRUE\nYbCdHg2,TRUE\nYbCe2CuS5,FALSE\nYbCe2CuSe5,FALSE\nYbCuGe,TRUE\nYbCuSi,TRUE\nYbDyPd2,TRUE\nYbGa2Pd,TRUE\nYbGeRh,TRUE\nYbH2ClO2,TRUE\nYbIn4Ni,TRUE\nYbIn4Rh,TRUE\nYbIr2,TRUE\nYbMgPd,TRUE\nYbMn2O5,TRUE\nYbNd2CuS5,FALSE\nYbNd3,TRUE\nYbNdAg2,TRUE\nYbPO4,TRUE\nYbPmPt2,TRUE\nYbPr11Se16,TRUE\nYbPr2CuS5,FALSE\nYbRh2,TRUE\nYbS,FALSE\nYbSb,FALSE\nYbSb4Te7,FALSE\nYbSe,FALSE\nYbSi2Ni,TRUE\nYbSm2CuS5,FALSE\nYbSmRh2,TRUE\nYbSn2Pd,TRUE\nYbSnRh,TRUE\nYbSnTe2,FALSE\nYbTe,FALSE\nYbTlS2,TRUE\nYbTlSe2,TRUE\nYbWClO4,FALSE\nYbZnAu2,TRUE\nYbZnPt,TRUE\nZn(Bi19O29)2,FALSE\nZn(CoO2)2,TRUE\nZn(CuO2)2,TRUE\nZn(FeN)2,TRUE\nZn(GaSe2)2,FALSE\nZn(InS2)2,FALSE\nZn(InSe2)2,FALSE\nZn(InTe2)2,FALSE\nZn0.01Cd0.99Se1,FALSE\nZn0.01Ga0.99As0.99Se0.01,FALSE\nZn0.01Ga0.99P0.99S0.01,FALSE\nZn0.01Ga0.99P0.99Se0.01,FALSE\nZn0.01Ga0.99Sb0.99Te0.01,FALSE\nZn0.05Ga0.95Sb0.95Te0.05,FALSE\nZn0.15Cd0.85Se1,FALSE\nZn0.15Ga0.85As0.85Se0.15,FALSE\nZn0.1Ga0.9Sb0.9Te0.1,FALSE\nZn0.25Ga0.75As0.75Se0.25,FALSE\nZn0.25Ga0.75P0.75Se0.25,FALSE\nZn0.2Ga0.8Sb0.8Te0.2,FALSE\nZn0.2Hg0.8Te1,FALSE\nZn0.3Ga0.7P0.7S0.3,FALSE\nZn0.42Ga0.58As0.58Se0.42,FALSE\nZn0.43Cd0.57Se1,FALSE\nZn0.4Hg0.6Se1,FALSE\nZn0.55Ga0.45P0.45S0.55,FALSE\nZn0.55Hg0.45Se1,FALSE\nZn0.5Cd0.5Se1,FALSE\nZn0.5Ga0.5As0.5Se0.5,FALSE\nZn0.5Ga0.5P0.5Se0.5,FALSE\nZn0.5Hg0.5Se1,FALSE\nZn0.65Hg0.35Se1,FALSE\nZn0.6Ga0.4As0.4Se0.6,FALSE\nZn0.75Cd0.25Se1,FALSE\nZn0.75Hg0.25Se1,FALSE\nZn0.75Hg0.25Te1,FALSE\nZn0.7Ga0.3As0.3Se0.7,FALSE\nZn0.7Ga0.3P0.3S0.7,FALSE\nZn0.7Ga0.3P0.3Se0.7,FALSE\nZn0.85Ga0.15As0.15Se0.85,FALSE\nZn0.85Ga0.15P0.15S0.85,FALSE\nZn0.85Hg0.15Se1,FALSE\nZn0.86Hg0.14Te1,FALSE\nZn0.8Hg0.2Se1,FALSE\nZn0.8Hg0.2Te1,FALSE\nZn0.92Hg0.08Te1,FALSE\nZn0.94Hg0.06Te1,FALSE\nZn0.95Ga0.05P0.05S0.95,FALSE\nZn0.95Ga0.05P0.05Se0.95,FALSE\nZn0.99Cd0.01Se1,FALSE\nZn0.99Ga0.01As0.01Se0.99,FALSE\nZn0.99Ga0.01P0.01S0.99,FALSE\nZn0.99Ga0.01P0.01Se0.99,FALSE\nZn0.99Ga0.01Sb0.01Te0.99,FALSE\nZn0.99Hg0.01Se1,FALSE\nZn0.99Hg0.01Te1,FALSE\nZn0.9Ga0.1As0.1Se0.9,FALSE\nZn0.9Ga0.1P0.1S0.9,FALSE\nZn0.9Ga0.1P0.1Se0.9,FALSE\nZn0.9Hg0.1Se1,FALSE\nZn0.9Hg0.1Te1,FALSE\nZn2BIr2,TRUE\nZn2In2S5,FALSE\nZn2InCuSe4,FALSE\nZn2InCuTe4,FALSE\nZn2MoSeO7,FALSE\nZn2Ni9O13,TRUE\nZn2Sb3O8,TRUE\nZn2SnN2,TRUE\nZn2TeMoO7,FALSE\nZn2WN2,TRUE\nZn3(BO3)2,FALSE\nZn3(InS3)2,FALSE\nZn3(PS4)2,FALSE\nZn3.5Ga1Sn0.5O6,FALSE\nZn3As2,FALSE\nZn3Cd,TRUE\nZn3Cu,TRUE\nZn3Cu10(TeO6)6,TRUE\nZn3N2,TRUE\nZn3P2,FALSE\nZn3Sb2,FALSE\nZn4.5Ga1Sn0.5O7,FALSE\nZn4Sb3,FALSE\nZn5.5Ga1Sn0.5O8,FALSE\nZn6S5Cl2,FALSE\nZn8Ag5,TRUE\nZnAgF5,TRUE\nZnAs,FALSE\nZnAs2,FALSE\nZnB12(H5O12)2,FALSE\nZnCrO2,TRUE\nZnCu2GeS4,FALSE\nZnCu2GeSe4,FALSE\nZnCu2SiS4,FALSE\nZnCu2SiSe4,FALSE\nZnCu2SiTe4,FALSE\nZnCu2SnSe4,FALSE\nZnCu2SnTe4,FALSE\nZnCu3P3O13,TRUE\nZnGaRh2,TRUE\nZnGeAs2,FALSE\nZnGeN2,FALSE\nZnGeP2,FALSE\nZnHg3(SCl2)2,FALSE\nZnHg3(SeCl2)2,FALSE\nZnI2,FALSE\nZnIrO3,TRUE\nZnO,FALSE\nZnS,FALSE\nZnSb,FALSE\nZnSb2MoO7,FALSE\nZnSb3,TRUE\nZnSe,FALSE\nZnSi(AgS2)2,FALSE\nZnSiAs2,FALSE\nZnSiP2,FALSE\nZnSn3,TRUE\nZnSnAs2,FALSE\nZnSnO3,FALSE\nZnSnP2,FALSE\nZnSnSb2,FALSE\nZnTc,FALSE\nZnTe,FALSE\nZnWO2,TRUE\nZr(Fe2Si)2,TRUE\nZr(Ni2P)2,TRUE\nZr0.67Ta1.33N3.03O0.12,FALSE\nZr1.33Ta0.67N1.63O1.89,FALSE\nZr1.33Ta0.67N1.97O1.38,FALSE\nZr1.33Ta0.67N2.61O0.42,FALSE\nZr1.86Cu1S4,FALSE\nZr2(Co7B2)3,TRUE\nZr2Al,TRUE\nZr2Co12P7,TRUE\nZr2CuS4,TRUE\nZr2HBr2,TRUE\nZr2In5Ni,TRUE\nZr2Ni12P7,TRUE\nZr2Se,TRUE\nZr2Te,TRUE\nZr3(Al2C3)2,TRUE\nZr3(Cu2Si3)2,TRUE\nZr3Ag,TRUE\nZr3Al2,TRUE\nZr3Hg,TRUE\nZr3Ir,TRUE\nZr3NiO,TRUE\nZr3O,FALSE\nZr4AlNi2,TRUE\nZr4Co4Ge7,TRUE\nZr5Al3,TRUE\nZr5Al3C,TRUE\nZr5Sb3,TRUE\nZr5SiSb3,TRUE\nZr5Sn3,TRUE\nZr5Sn4,TRUE\nZr6Al2CoH10,TRUE\nZr6Al2Ni,TRUE\nZr6NiCl15,TRUE\nZr6O,FALSE\nZr6Sb2Pt,TRUE\nZr7P4,TRUE\nZr7Sb4,TRUE\nZrAl5Ni2,TRUE\nZrAlPt,TRUE\nZrAlRu2,TRUE\nZrAlW,TRUE\nZrAu4,TRUE\nZrB2,TRUE\nZrC,FALSE\nZrCd,TRUE\nZrCrSi2,TRUE\nZrGaPt,TRUE\nZrGe2,TRUE\nZrGeRu,TRUE\nZrHCl,TRUE\nZrHg4(AsCl3)2,FALSE\nZrHg4(PCl3)2,FALSE\nZrInCu2,TRUE\nZrInPd2,TRUE\nZrInRh2,TRUE\nZrIr2,TRUE\nZrMo3,TRUE\nZrNiGe,TRUE\nZrNiSb,FALSE\nZrNiSn,TRUE\nZrO2,FALSE\nZrPd2,TRUE\nZrPd3,TRUE\nZrRe2,TRUE\nZrRh,TRUE\nZrRu3C,TRUE\nZrS2,FALSE\nZrS3,FALSE\nZrSb,TRUE\nZrSbRu,TRUE\nZrSe,TRUE\nZrSe2,FALSE\nZrSe3,FALSE\nZrSi2,TRUE\nZrSiTe,TRUE\nZrTaN3,FALSE\nZrTe,TRUE\nZrTi2O,TRUE\nZrTiF6,TRUE\nZrW2,TRUE\n"
  },
  {
    "path": "dataset/matbench_is_metal/matbench_is_metal.json",
    "content": "[\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In5AgTe8\\n\",\n        \"output\": \" No, In5AgTe8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsTbZnTe3\\n\",\n        \"output\": \" No, CsTbZnTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiHoO3\\n\",\n        \"output\": \" Yes, LiHoO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbCuSi\\n\",\n        \"output\": \" Yes, YbCuSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaTl\\n\",\n        \"output\": \" Yes, NaTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb4Ge(PSe3)4\\n\",\n        \"output\": \" No, Rb4Ge(PSe3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DySn3\\n\",\n        \"output\": \" Yes, DySn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuBiSO\\n\",\n        \"output\": \" No, CuBiSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScCdHg2\\n\",\n        \"output\": \" Yes, ScCdHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2In\\n\",\n        \"output\": \" Yes, La2In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdCu2SnS4\\n\",\n        \"output\": \" No, CdCu2SnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiTaO3\\n\",\n        \"output\": \" No, LiTaO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Fe6W6C\\n\",\n        \"output\": \" Yes, Fe6W6C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrSb\\n\",\n        \"output\": \" No, PrSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu4C7\\n\",\n        \"output\": \" Yes, Lu4C7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al6Tc\\n\",\n        \"output\": \" Yes, Al6Tc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" price\\n\",\n        \"output\": \" price is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm(NiGe)2\\n\",\n        \"output\": \" Yes, Tm(NiGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf5Pb\\n\",\n        \"output\": \" Yes, Hf5Pb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KZrPSe6\\n\",\n        \"output\": \" No, KZrPSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbBi3Se5\\n\",\n        \"output\": \" No, RbBi3Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnCu3\\n\",\n        \"output\": \" Yes, MnCu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaF2\\n\",\n        \"output\": \" No, BaF2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cr(MoS2)2\\n\",\n        \"output\": \" Yes, Cr(MoS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu2AlTc\\n\",\n        \"output\": \" Yes, Lu2AlTc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Te2W2SeS\\n\",\n        \"output\": \" Yes, Te2W2SeS is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PPdS\\n\",\n        \"output\": \" No, PPdS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaCuSbS3\\n\",\n        \"output\": \" No, BaCuSbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr8Co8O23\\n\",\n        \"output\": \" Yes, Sr8Co8O23 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga4Cu2Te7\\n\",\n        \"output\": \" No, Ga4Cu2Te7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Ge2PbS6\\n\",\n        \"output\": \" No, K2Ge2PbS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cr2CuS4\\n\",\n        \"output\": \" Yes, Cr2CuS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li23(MnAs)20\\n\",\n        \"output\": \" Yes, Li23(MnAs)20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmAs\\n\",\n        \"output\": \" No, SmAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Fe3B\\n\",\n        \"output\": \" Yes, Fe3B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiLu2Pd\\n\",\n        \"output\": \" Yes, LiLu2Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiSeI\\n\",\n        \"output\": \" No, BiSeI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TcB\\n\",\n        \"output\": \" Yes, TcB is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiCu5P3O13\\n\",\n        \"output\": \" Yes, LiCu5P3O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" dad\\n\",\n        \"output\": \" dad is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbDyPd2\\n\",\n        \"output\": \" Yes, YbDyPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl(WO3)3\\n\",\n        \"output\": \" Yes, Tl(WO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Fe(SbO3)4\\n\",\n        \"output\": \" Yes, Li3Fe(SbO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeMgPt\\n\",\n        \"output\": \" Yes, CeMgPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmBPd3\\n\",\n        \"output\": \" Yes, TmBPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn3Cr3(TeO8)2\\n\",\n        \"output\": \" Yes, Mn3Cr3(TeO8)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag2GeS3\\n\",\n        \"output\": \" No, Ag2GeS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfB4Ir3\\n\",\n        \"output\": \" Yes, HfB4Ir3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PmMgAu2\\n\",\n        \"output\": \" Yes, PmMgAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U3Bi4\\n\",\n        \"output\": \" Yes, U3Bi4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UAlNi4\\n\",\n        \"output\": \" Yes, UAlNi4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrSbRu\\n\",\n        \"output\": \" Yes, ZrSbRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SbTeI\\n\",\n        \"output\": \" No, SbTeI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al0.45Cd0.55Sb0.45Te0.55\\n\",\n        \"output\": \" No, Al0.45Cd0.55Sb0.45Te0.55 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3Sn2S7\\n\",\n        \"output\": \" Yes, Ca3Sn2S7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbNiO3\\n\",\n        \"output\": \" Yes, TbNiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Cd3Te4\\n\",\n        \"output\": \" No, Cs2Cd3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrIn2Ir\\n\",\n        \"output\": \" Yes, SrIn2Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2YGaSe5\\n\",\n        \"output\": \" No, Ba2YGaSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pb1Se0.95S0.05\\n\",\n        \"output\": \" No, Pb1Se0.95S0.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K11Mn4O16\\n\",\n        \"output\": \" Yes, K11Mn4O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ReCl4\\n\",\n        \"output\": \" Yes, ReCl4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.2Te1Pb0.8\\n\",\n        \"output\": \" No, Sn0.2Te1Pb0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbIn4\\n\",\n        \"output\": \" Yes, RbIn4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb2I2F11\\n\",\n        \"output\": \" Yes, Sb2I2F11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In4S5\\n\",\n        \"output\": \" No, In4S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Te2.7Se0.3\\n\",\n        \"output\": \" No, Bi2Te2.7Se0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaCuGeSe4\\n\",\n        \"output\": \" No, GaCuGeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nb5Ga4\\n\",\n        \"output\": \" Yes, Nb5Ga4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd4(GeS4)3\\n\",\n        \"output\": \" No, Nd4(GeS4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrLaMn2O6\\n\",\n        \"output\": \" Yes, SrLaMn2O6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Te0.9Se2.1\\n\",\n        \"output\": \" No, Bi2Te0.9Se2.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca6Ag16N\\n\",\n        \"output\": \" Yes, Ca6Ag16N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AlAgS2\\n\",\n        \"output\": \" No, AlAgS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2VCuS4\\n\",\n        \"output\": \" No, Rb2VCuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgTe2As\\n\",\n        \"output\": \" No, AgTe2As is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsInHgS3\\n\",\n        \"output\": \" No, CsInHgS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2SmInTe5\\n\",\n        \"output\": \" No, Ba2SmInTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiMgSnPd\\n\",\n        \"output\": \" Yes, LiMgSnPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaNaB5O9\\n\",\n        \"output\": \" No, BaNaB5O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoTiO3\\n\",\n        \"output\": \" Yes, HoTiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2Cu2SnS4\\n\",\n        \"output\": \" No, Tl2Cu2SnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4LiGa5Se12\\n\",\n        \"output\": \" No, Ba4LiGa5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuSiIr\\n\",\n        \"output\": \" Yes, LuSiIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca(Al4Co)2\\n\",\n        \"output\": \" Yes, Ca(Al4Co)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KNa2Sb\\n\",\n        \"output\": \" No, KNa2Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SnAs3\\n\",\n        \"output\": \" Yes, SnAs3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2In2SiS6\\n\",\n        \"output\": \" No, Na2In2SiS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(SmS2)2\\n\",\n        \"output\": \" No, Ca(SmS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaIn5Ir\\n\",\n        \"output\": \" Yes, LaIn5Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyInAu\\n\",\n        \"output\": \" Yes, DyInAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In3CuTe5\\n\",\n        \"output\": \" No, In3CuTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdErZn2\\n\",\n        \"output\": \" Yes, NdErZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li6Mn5FeO12\\n\",\n        \"output\": \" Yes, Li6Mn5FeO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbZnAu2\\n\",\n        \"output\": \" Yes, YbZnAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsAg2TeS6\\n\",\n        \"output\": \" No, CsAg2TeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr2Cu(ClO)2\\n\",\n        \"output\": \" Yes, Sr2Cu(ClO)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaTiO2\\n\",\n        \"output\": \" Yes, CaTiO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiFe2(SiO4)2\\n\",\n        \"output\": \" Yes, LiFe2(SiO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" As2O3\\n\",\n        \"output\": \" No, As2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.1Ga0.9As0.1P0.9\\n\",\n        \"output\": \" No, In0.1Ga0.9As0.1P0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaDy2CuO5\\n\",\n        \"output\": \" Yes, BaDy2CuO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.99Hg0.01Te1\\n\",\n        \"output\": \" No, Zn0.99Hg0.01Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb5(WO3)18\\n\",\n        \"output\": \" Yes, Rb5(WO3)18 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs3Sb2Br9\\n\",\n        \"output\": \" No, Cs3Sb2Br9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoAlB14\\n\",\n        \"output\": \" Yes, HoAlB14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba(GaS2)2\\n\",\n        \"output\": \" No, Ba(GaS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn(BW)2\\n\",\n        \"output\": \" Yes, Mn(BW)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce5(SiN3)3\\n\",\n        \"output\": \" Yes, Ce5(SiN3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd0.4Hg0.6Se1\\n\",\n        \"output\": \" No, Cd0.4Hg0.6Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu2TlCu3Se5\\n\",\n        \"output\": \" No, Lu2TlCu3Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K10Mn4Sn4S17\\n\",\n        \"output\": \" No, K10Mn4Sn4S17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuUO3\\n\",\n        \"output\": \" Yes, LuUO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U3Ni3Sn4\\n\",\n        \"output\": \" Yes, U3Ni3Sn4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TcSe2\\n\",\n        \"output\": \" No, TcSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cr3N2\\n\",\n        \"output\": \" Yes, Cr3N2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfC\\n\",\n        \"output\": \" Yes, HfC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2NiH\\n\",\n        \"output\": \" Yes, Ti2NiH is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Te2Mo\\n\",\n        \"output\": \" No, Te2Mo is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn0.2Te0.2Pb0.8Se0.8\\n\",\n        \"output\": \" No, Sn0.2Te0.2Pb0.8Se0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm(SiNi)2\\n\",\n        \"output\": \" Yes, Sm(SiNi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn2BiSI5\\n\",\n        \"output\": \" No, Sn2BiSI5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu4Te7\\n\",\n        \"output\": \" No, Eu4Te7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1Sb0.3As0.7\\n\",\n        \"output\": \" No, In1Sb0.3As0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs3As\\n\",\n        \"output\": \" No, Cs3As is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.5In2.2Ag0.4Te4\\n\",\n        \"output\": \" No, Cd0.5In2.2Ag0.4Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlPd5I2\\n\",\n        \"output\": \" Yes, AlPd5I2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr2S3\\n\",\n        \"output\": \" No, Pr2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3V4FeO12\\n\",\n        \"output\": \" Yes, Li3V4FeO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K3UF3\\n\",\n        \"output\": \" Yes, K3UF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeCuSe2\\n\",\n        \"output\": \" No, FeCuSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2YbCuSe5\\n\",\n        \"output\": \" No, La2YbCuSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb2Tl4S11\\n\",\n        \"output\": \" No, Nb2Tl4S11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti9O8\\n\",\n        \"output\": \" Yes, Ti9O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiCa2Ga\\n\",\n        \"output\": \" Yes, LiCa2Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuNiGe3\\n\",\n        \"output\": \" Yes, EuNiGe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdTeO3\\n\",\n        \"output\": \" No, CdTeO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbSnRh\\n\",\n        \"output\": \" Yes, YbSnRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti2Sb(PO4)3\\n\",\n        \"output\": \" Yes, Ti2Sb(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd4Sb2I3\\n\",\n        \"output\": \" No, Cd4Sb2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga3CuTe5\\n\",\n        \"output\": \" No, Ga3CuTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2PmAl\\n\",\n        \"output\": \" Yes, Li2PmAl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbV(CuS2)2\\n\",\n        \"output\": \" No, RbV(CuS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiInAg2\\n\",\n        \"output\": \" Yes, LiInAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn3Pd\\n\",\n        \"output\": \" Yes, Sn3Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Co3W\\n\",\n        \"output\": \" Yes, Co3W is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf2Fe\\n\",\n        \"output\": \" Yes, Hf2Fe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu3SbSe4\\n\",\n        \"output\": \" No, Cu3SbSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrMnGe\\n\",\n        \"output\": \" Yes, SrMnGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Er2O3\\n\",\n        \"output\": \" No, Er2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Co2Ge\\n\",\n        \"output\": \" Yes, Co2Ge is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YIn2Ni\\n\",\n        \"output\": \" Yes, YIn2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al4Cu2O7\\n\",\n        \"output\": \" Yes, Al4Cu2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyIr2\\n\",\n        \"output\": \" Yes, DyIr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmInAu\\n\",\n        \"output\": \" Yes, SmInAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbH3(SeO3)2\\n\",\n        \"output\": \" No, RbH3(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PbS\\n\",\n        \"output\": \" No, PbS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K4Ge(PSe3)4\\n\",\n        \"output\": \" No, K4Ge(PSe3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm5(Ge5Rh2)2\\n\",\n        \"output\": \" Yes, Tm5(Ge5Rh2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2Ti3FeO8\\n\",\n        \"output\": \" Yes, Li2Ti3FeO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc5Pb3\\n\",\n        \"output\": \" Yes, Sc5Pb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy(CoGe)2\\n\",\n        \"output\": \" Yes, Dy(CoGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SiSb\\n\",\n        \"output\": \" No, SiSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaSiAgSe4\\n\",\n        \"output\": \" No, GaSiAgSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li6FeO6\\n\",\n        \"output\": \" Yes, Li6FeO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y4CuTe8\\n\",\n        \"output\": \" Yes, Y4CuTe8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KPSe6\\n\",\n        \"output\": \" No, KPSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Cr3(CuO6)2\\n\",\n        \"output\": \" Yes, Li3Cr3(CuO6)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2GaSbSe5\\n\",\n        \"output\": \" No, Ba2GaSbSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy12C6I17\\n\",\n        \"output\": \" Yes, Dy12C6I17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs3NaZn2Ge21\\n\",\n        \"output\": \" No, Cs3NaZn2Ge21 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaMg(FeO3)2\\n\",\n        \"output\": \" Yes, LaMg(FeO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HfAs2\\n\",\n        \"output\": \" Yes, HfAs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgPdO2\\n\",\n        \"output\": \" Yes, AgPdO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnSb3\\n\",\n        \"output\": \" Yes, ZnSb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbSb2\\n\",\n        \"output\": \" Yes, TbSb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La1.86Tb1.14Ga1.67S7\\n\",\n        \"output\": \" No, La1.86Tb1.14Ga1.67S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyCd2\\n\",\n        \"output\": \" Yes, DyCd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb2Tl3CuSe12\\n\",\n        \"output\": \" No, Nb2Tl3CuSe12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsInGeS4\\n\",\n        \"output\": \" No, CsInGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfTc\\n\",\n        \"output\": \" Yes, HfTc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc2TlTc\\n\",\n        \"output\": \" Yes, Sc2TlTc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn5(BRh3)2\\n\",\n        \"output\": \" Yes, Sn5(BRh3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrB4\\n\",\n        \"output\": \" Yes, PrB4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2SnIr\\n\",\n        \"output\": \" Yes, Li2SnIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2GaSbTe5\\n\",\n        \"output\": \" No, Ba2GaSbTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2ReNiO6\\n\",\n        \"output\": \" Yes, Ba2ReNiO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Co2O3\\n\",\n        \"output\": \" Yes, Co2O3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn3SbO8\\n\",\n        \"output\": \" Yes, Mn3SbO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CoMoP2\\n\",\n        \"output\": \" Yes, CoMoP2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs3Li4(BO2)7\\n\",\n        \"output\": \" No, Cs3Li4(BO2)7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2GeSe5\\n\",\n        \"output\": \" No, La2GeSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs3Bi2I9\\n\",\n        \"output\": \" No, Cs3Bi2I9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KMo6S7\\n\",\n        \"output\": \" Yes, KMo6S7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuBr\\n\",\n        \"output\": \" No, CuBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1.6Cu0.4Se2.6\\n\",\n        \"output\": \" No, In1.6Cu0.4Se2.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2VCoO6\\n\",\n        \"output\": \" No, La2VCoO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2GaBiSe5\\n\",\n        \"output\": \" No, Ba2GaBiSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1As0.5P0.5\\n\",\n        \"output\": \" No, Ga1As0.5P0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeTlZn\\n\",\n        \"output\": \" Yes, CeTlZn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mo5O14\\n\",\n        \"output\": \" Yes, Mo5O14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr(In4Rh)2\\n\",\n        \"output\": \" Yes, Sr(In4Rh)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" secure\\n\",\n        \"output\": \" secure is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K3Ga3Ge7Se20\\n\",\n        \"output\": \" No, K3Ga3Ge7Se20 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UVC2\\n\",\n        \"output\": \" Yes, UVC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCdBO3\\n\",\n        \"output\": \" No, CsCdBO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScCd\\n\",\n        \"output\": \" No, ScCd is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGe4(RhSe3)2\\n\",\n        \"output\": \" No, BaGe4(RhSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AsP\\n\",\n        \"output\": \" No, AsP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YSbPt\\n\",\n        \"output\": \" No, YSbPt is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlB2\\n\",\n        \"output\": \" Yes, AlB2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Te1.5Se1.5\\n\",\n        \"output\": \" No, Bi2Te1.5Se1.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" kohlrabi\\n\",\n        \"output\": \" kohlrabi is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd3As2\\n\",\n        \"output\": \" No, Cd3As2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaIn3Se5\\n\",\n        \"output\": \" No, NaIn3Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TePb\\n\",\n        \"output\": \" No, TePb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U2AlCo2\\n\",\n        \"output\": \" Yes, U2AlCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y(TiGa2)2\\n\",\n        \"output\": \" Yes, Y(TiGa2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiInS2\\n\",\n        \"output\": \" No, LiInS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3(CuO)4\\n\",\n        \"output\": \" Yes, Li3(CuO)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GePt2\\n\",\n        \"output\": \" Yes, GePt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4Nb14O23\\n\",\n        \"output\": \" Yes, Ba4Nb14O23 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu2CdIn\\n\",\n        \"output\": \" Yes, Lu2CdIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiFe2\\n\",\n        \"output\": \" Yes, TiFe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3Eu(PO4)3\\n\",\n        \"output\": \" No, Ba3Eu(PO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2IO2\\n\",\n        \"output\": \" Yes, Sm2IO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.15Pb0.85Se0.85S0.15\\n\",\n        \"output\": \" No, Ge0.15Pb0.85Se0.85S0.15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2LaIrO6\\n\",\n        \"output\": \" Yes, Ba2LaIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi3Se2NO11\\n\",\n        \"output\": \" No, Bi3Se2NO11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn2BIr2\\n\",\n        \"output\": \" Yes, Zn2BIr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VIr3\\n\",\n        \"output\": \" Yes, VIr3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnSnAs2\\n\",\n        \"output\": \" No, ZnSnAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2Sn2Hg3S8\\n\",\n        \"output\": \" No, Na2Sn2Hg3S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La20Cu9O40\\n\",\n        \"output\": \" Yes, La20Cu9O40 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ThAl\\n\",\n        \"output\": \" Yes, ThAl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmAu2\\n\",\n        \"output\": \" Yes, TmAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaAu(IO3)5\\n\",\n        \"output\": \" No, BaAu(IO3)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnSiAs2\\n\",\n        \"output\": \" No, ZnSiAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGa4S7\\n\",\n        \"output\": \" No, BaGa4S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" fedelini\\n\",\n        \"output\": \" fedelini is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.25Ga0.75As0.75Se0.25\\n\",\n        \"output\": \" No, Zn0.25Ga0.75As0.75Se0.25 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U2Ti\\n\",\n        \"output\": \" Yes, U2Ti is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" letter\\n\",\n        \"output\": \" letter is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm(CoSi)2\\n\",\n        \"output\": \" Yes, Tm(CoSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.35Te0.35Pb0.65Se0.65\\n\",\n        \"output\": \" No, Sn0.35Te0.35Pb0.65Se0.65 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce(SiAu)2\\n\",\n        \"output\": \" Yes, Ce(SiAu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGa2SiS6\\n\",\n        \"output\": \" No, BaGa2SiS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmSnRh\\n\",\n        \"output\": \" Yes, TmSnRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeF3\\n\",\n        \"output\": \" No, CeF3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RuSe2\\n\",\n        \"output\": \" No, RuSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BeAlB\\n\",\n        \"output\": \" Yes, BeAlB is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RuCl3\\n\",\n        \"output\": \" Yes, RuCl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" InN\\n\",\n        \"output\": \" No, InN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na3UF7\\n\",\n        \"output\": \" Yes, Na3UF7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca(CoS2)4\\n\",\n        \"output\": \" Yes, Ca(CoS2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2Te\\n\",\n        \"output\": \" No, Cs2Te is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al2(CuSe2)3\\n\",\n        \"output\": \" Yes, Al2(CuSe2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdSb\\n\",\n        \"output\": \" Yes, NdSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu3InN\\n\",\n        \"output\": \" Yes, Lu3InN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu2SnSe3\\n\",\n        \"output\": \" No, Cu2SnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ReF6\\n\",\n        \"output\": \" Yes, ReF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.5Hg0.5Se1\\n\",\n        \"output\": \" No, Cd0.5Hg0.5Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PmCdPd2\\n\",\n        \"output\": \" Yes, PmCdPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuF\\n\",\n        \"output\": \" Yes, CuF is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" B3Pb3NO10\\n\",\n        \"output\": \" No, B3Pb3NO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn3Sb2\\n\",\n        \"output\": \" No, Zn3Sb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi2(PO4)3\\n\",\n        \"output\": \" Yes, Bi2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2ZnSnS4\\n\",\n        \"output\": \" No, Li2ZnSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ThFe2SiC\\n\",\n        \"output\": \" Yes, ThFe2SiC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu3Se2(ClO3)2\\n\",\n        \"output\": \" Yes, Cu3Se2(ClO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" P4Os\\n\",\n        \"output\": \" No, P4Os is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyBiPt\\n\",\n        \"output\": \" Yes, DyBiPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbMn5Ge3\\n\",\n        \"output\": \" Yes, TbMn5Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2TeI6\\n\",\n        \"output\": \" No, K2TeI6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" screwdriver\\n\",\n        \"output\": \" screwdriver is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu3(InP2)2\\n\",\n        \"output\": \" No, Eu3(InP2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SiAu3\\n\",\n        \"output\": \" Yes, SiAu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn4.5Ga1Sn0.5O7\\n\",\n        \"output\": \" No, Zn4.5Ga1Sn0.5O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SnSe\\n\",\n        \"output\": \" No, SnSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2CdPb\\n\",\n        \"output\": \" Yes, Ca2CdPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb5OF14\\n\",\n        \"output\": \" Yes, Nb5OF14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2CrCo3O8\\n\",\n        \"output\": \" Yes, Li2CrCo3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2La1.19Bi8.81S16\\n\",\n        \"output\": \" No, Cs2La1.19Bi8.81S16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeAlSi2\\n\",\n        \"output\": \" Yes, CeAlSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PPdSe\\n\",\n        \"output\": \" No, PPdSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UP2S7\\n\",\n        \"output\": \" No, UP2S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaCdAg2\\n\",\n        \"output\": \" Yes, LaCdAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na3Tl\\n\",\n        \"output\": \" Yes, Na3Tl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Sb\\n\",\n        \"output\": \" No, Cs2Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" emery\\n\",\n        \"output\": \" emery is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrCu2Si\\n\",\n        \"output\": \" Yes, CrCu2Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AsRuS\\n\",\n        \"output\": \" No, AsRuS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SiSn\\n\",\n        \"output\": \" No, SiSn is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba5In4Te4S7\\n\",\n        \"output\": \" No, Ba5In4Te4S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce5Si3\\n\",\n        \"output\": \" Yes, Ce5Si3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GeS2\\n\",\n        \"output\": \" No, GeS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.01Te1Pb0.99\\n\",\n        \"output\": \" No, In0.01Te1Pb0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlAgTe2\\n\",\n        \"output\": \" No, TlAgTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti2CoGe\\n\",\n        \"output\": \" Yes, Ti2CoGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca3Cu2(ClO2)2\\n\",\n        \"output\": \" Yes, Ca3Cu2(ClO2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnI2\\n\",\n        \"output\": \" No, MnI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba(PdO2)2\\n\",\n        \"output\": \" Yes, Ba(PdO2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr2GeC\\n\",\n        \"output\": \" Yes, Cr2GeC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb2(CoO3)3\\n\",\n        \"output\": \" Yes, Nb2(CoO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TeSe3\\n\",\n        \"output\": \" No, TeSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr4MgRu\\n\",\n        \"output\": \" Yes, Pr4MgRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3CrO4\\n\",\n        \"output\": \" Yes, Li3CrO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FeCuTe2\\n\",\n        \"output\": \" No, FeCuTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb4Al2O9\\n\",\n        \"output\": \" No, Tb4Al2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn(SbO3)2\\n\",\n        \"output\": \" Yes, Mn(SbO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Hg3Se1.49S2.51\\n\",\n        \"output\": \" No, Na2Hg3Se1.49S2.51 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaCdSnS4\\n\",\n        \"output\": \" No, BaCdSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu4H10SO12\\n\",\n        \"output\": \" Yes, Cu4H10SO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf3P3Pd4\\n\",\n        \"output\": \" Yes, Hf3P3Pd4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbYbZnSe3\\n\",\n        \"output\": \" No, RbYbZnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu3BC3\\n\",\n        \"output\": \" Yes, Lu3BC3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2B4Rh5\\n\",\n        \"output\": \" Yes, La2B4Rh5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YTmCu2\\n\",\n        \"output\": \" Yes, YTmCu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" digger\\n\",\n        \"output\": \" digger is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaFe2(SiO3)4\\n\",\n        \"output\": \" Yes, NaFe2(SiO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbCu5\\n\",\n        \"output\": \" Yes, TbCu5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmMgAg2\\n\",\n        \"output\": \" Yes, TmMgAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy2AlCo2\\n\",\n        \"output\": \" Yes, Dy2AlCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Cd3Se4\\n\",\n        \"output\": \" No, K2Cd3Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" U(CoGe)2\\n\",\n        \"output\": \" Yes, U(CoGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbCuGe\\n\",\n        \"output\": \" Yes, YbCuGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2CrN3\\n\",\n        \"output\": \" Yes, Ce2CrN3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta11(CuO15)2\\n\",\n        \"output\": \" No, Ta11(CuO15)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg2SiPt\\n\",\n        \"output\": \" Yes, Mg2SiPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2PbSe4\\n\",\n        \"output\": \" No, Ga2PbSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" UGa3Ni\\n\",\n        \"output\": \" Yes, UGa3Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga0.95Hg0.05Sb0.95Te0.05\\n\",\n        \"output\": \" No, Ga0.95Hg0.05Sb0.95Te0.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba8Ta7O24\\n\",\n        \"output\": \" Yes, Ba8Ta7O24 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm(MnGe)2\\n\",\n        \"output\": \" Yes, Sm(MnGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy5Sn3\\n\",\n        \"output\": \" Yes, Dy5Sn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg3Ge\\n\",\n        \"output\": \" Yes, Mg3Ge is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BeSiRu2\\n\",\n        \"output\": \" Yes, BeSiRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnCu2SiTe4\\n\",\n        \"output\": \" No, ZnCu2SiTe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pb1Se0.9S0.1\\n\",\n        \"output\": \" No, Pb1Se0.9S0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn(GaSe2)2\\n\",\n        \"output\": \" No, Zn(GaSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdPt\\n\",\n        \"output\": \" Yes, NdPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiB3\\n\",\n        \"output\": \" No, LiB3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdSb4MoO10\\n\",\n        \"output\": \" No, CdSb4MoO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" pimple\\n\",\n        \"output\": \" pimple is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3ErRu2O9\\n\",\n        \"output\": \" Yes, Ba3ErRu2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg10B16Ir19\\n\",\n        \"output\": \" Yes, Mg10B16Ir19 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdCu(SeO3)2\\n\",\n        \"output\": \" No, CdCu(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2VNiO6\\n\",\n        \"output\": \" No, La2VNiO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K3Hg\\n\",\n        \"output\": \" Yes, K3Hg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2V3CrO8\\n\",\n        \"output\": \" Yes, Li2V3CrO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BeSe\\n\",\n        \"output\": \" No, BeSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmCuO3\\n\",\n        \"output\": \" Yes, SmCuO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ir0.67Se2\\n\",\n        \"output\": \" No, Ir0.67Se2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn3.5Ga1Sn0.5O6\\n\",\n        \"output\": \" No, Zn3.5Ga1Sn0.5O6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y3Al3NiGe2\\n\",\n        \"output\": \" Yes, Y3Al3NiGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2In2SiSe6\\n\",\n        \"output\": \" No, Li2In2SiSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Mo9Se10\\n\",\n        \"output\": \" Yes, Rb2Mo9Se10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrB2\\n\",\n        \"output\": \" Yes, SrB2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2Te\\n\",\n        \"output\": \" No, Rb2Te is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm6Br13\\n\",\n        \"output\": \" Yes, Sm6Br13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.01Te1Pb0.99\\n\",\n        \"output\": \" No, Ge0.01Te1Pb0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi5IO7\\n\",\n        \"output\": \" No, Bi5IO7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta2Mn3O8\\n\",\n        \"output\": \" No, Ta2Mn3O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er(SiPd)2\\n\",\n        \"output\": \" Yes, Er(SiPd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu(ZnGe)2\\n\",\n        \"output\": \" Yes, Eu(ZnGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UAl4\\n\",\n        \"output\": \" Yes, UAl4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu2PHO5\\n\",\n        \"output\": \" Yes, Cu2PHO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl0.07Te1Pb0.93\\n\",\n        \"output\": \" No, Tl0.07Te1Pb0.93 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.1Ga0.9Sb0.9Te0.1\\n\",\n        \"output\": \" No, Zn0.1Ga0.9Sb0.9Te0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr2CoReO6\\n\",\n        \"output\": \" Yes, Sr2CoReO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaNbSe2O7\\n\",\n        \"output\": \" No, NaNbSe2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm(CuO2)2\\n\",\n        \"output\": \" Yes, Sm(CuO2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrMgSnSe4\\n\",\n        \"output\": \" No, SrMgSnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErBiW2O9\\n\",\n        \"output\": \" No, ErBiW2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm(CoSi)2\\n\",\n        \"output\": \" Yes, Sm(CoSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al9Co2\\n\",\n        \"output\": \" Yes, Al9Co2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2Hg5\\n\",\n        \"output\": \" Yes, Mn2Hg5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbCe2CuSe5\\n\",\n        \"output\": \" No, YbCe2CuSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeMgNi4\\n\",\n        \"output\": \" Yes, CeMgNi4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.001Te1Pb0.999\\n\",\n        \"output\": \" No, Sn0.001Te1Pb0.999 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Au(IO3)5\\n\",\n        \"output\": \" No, K2Au(IO3)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K4Ce3Sn3S14\\n\",\n        \"output\": \" No, K4Ce3Sn3S14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr(MnSi)2\\n\",\n        \"output\": \" Yes, Pr(MnSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2Ga2S5\\n\",\n        \"output\": \" No, Cs2Ga2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ash\\n\",\n        \"output\": \" ash is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho(BC)2\\n\",\n        \"output\": \" Yes, Ho(BC)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu3Sb4S9\\n\",\n        \"output\": \" No, Eu3Sb4S9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Th2In\\n\",\n        \"output\": \" Yes, Th2In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U3Nb\\n\",\n        \"output\": \" Yes, U3Nb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm2(SnSe3)3\\n\",\n        \"output\": \" No, Sm2(SnSe3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho3Pd2\\n\",\n        \"output\": \" Yes, Ho3Pd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y4US5O3\\n\",\n        \"output\": \" No, Y4US5O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca3Sb2\\n\",\n        \"output\": \" No, Ca3Sb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc2GaAg\\n\",\n        \"output\": \" Yes, Sc2GaAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoInPt\\n\",\n        \"output\": \" Yes, HoInPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnB\\n\",\n        \"output\": \" Yes, SnB is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbNdAg2\\n\",\n        \"output\": \" Yes, YbNdAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YTiO3\\n\",\n        \"output\": \" Yes, YTiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V8O\\n\",\n        \"output\": \" Yes, V8O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.94Hg0.06Te1\\n\",\n        \"output\": \" No, Zn0.94Hg0.06Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Nb4Se4O19\\n\",\n        \"output\": \" No, Na2Nb4Se4O19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdHIO4\\n\",\n        \"output\": \" No, CdHIO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3Bi2TeO9\\n\",\n        \"output\": \" No, Ba3Bi2TeO9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb5Tl3O\\n\",\n        \"output\": \" Yes, Rb5Tl3O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YHg2\\n\",\n        \"output\": \" Yes, YHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrSe\\n\",\n        \"output\": \" No, SrSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2SnHgS4\\n\",\n        \"output\": \" No, Li2SnHgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KNb3(TeO6)2\\n\",\n        \"output\": \" No, KNb3(TeO6)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbTbSe2\\n\",\n        \"output\": \" No, RbTbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hf54Os17\\n\",\n        \"output\": \" Yes, Hf54Os17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd2O3\\n\",\n        \"output\": \" No, Gd2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li7Ti16O32\\n\",\n        \"output\": \" Yes, Li7Ti16O32 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiHoAu2\\n\",\n        \"output\": \" Yes, LiHoAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Sn3(SbS5)2\\n\",\n        \"output\": \" No, K2Sn3(SbS5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La10Si8O3\\n\",\n        \"output\": \" Yes, La10Si8O3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1.9Cu0.1Se2.9\\n\",\n        \"output\": \" No, In1.9Cu0.1Se2.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In9AgTe14\\n\",\n        \"output\": \" No, In9AgTe14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdAg2GeS4\\n\",\n        \"output\": \" No, CdAg2GeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2B10H9O\\n\",\n        \"output\": \" Yes, K2B10H9O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pm3I\\n\",\n        \"output\": \" Yes, Pm3I is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" W3O7F\\n\",\n        \"output\": \" Yes, W3O7F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiFe2Sb\\n\",\n        \"output\": \" Yes, TiFe2Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu2PBr\\n\",\n        \"output\": \" Yes, Eu2PBr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.01Ga0.99As0.99Se0.01\\n\",\n        \"output\": \" No, Zn0.01Ga0.99As0.99Se0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2InAg\\n\",\n        \"output\": \" Yes, Li2InAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb2GeS5\\n\",\n        \"output\": \" No, Tb2GeS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GePb2(SeO3)4\\n\",\n        \"output\": \" No, GePb2(SeO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrCrSi2\\n\",\n        \"output\": \" Yes, ZrCrSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U2Al3C4\\n\",\n        \"output\": \" Yes, U2Al3C4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CrNiP2O9\\n\",\n        \"output\": \" Yes, CrNiP2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca11Bi10\\n\",\n        \"output\": \" Yes, Ca11Bi10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HoTh3\\n\",\n        \"output\": \" Yes, HoTh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta2MoOs\\n\",\n        \"output\": \" Yes, Ta2MoOs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnCu2SiSe4\\n\",\n        \"output\": \" No, ZnCu2SiSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf4Co4Si7\\n\",\n        \"output\": \" Yes, Hf4Co4Si7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er2(Ga3Co)3\\n\",\n        \"output\": \" Yes, Er2(Ga3Co)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3Re\\n\",\n        \"output\": \" Yes, V3Re is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" degree\\n\",\n        \"output\": \" degree is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CoSbS\\n\",\n        \"output\": \" No, CoSbS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" canada\\n\",\n        \"output\": \" canada is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy2MgTl\\n\",\n        \"output\": \" Yes, Dy2MgTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn(InS2)2\\n\",\n        \"output\": \" No, Zn(InS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce(CoB)4\\n\",\n        \"output\": \" Yes, Ce(CoB)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NbSe2\\n\",\n        \"output\": \" No, NbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.3Te1Pb0.7\\n\",\n        \"output\": \" No, Ge0.3Te1Pb0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb2EuSe4\\n\",\n        \"output\": \" No, Yb2EuSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U4S3\\n\",\n        \"output\": \" Yes, U4S3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" click\\n\",\n        \"output\": \" click is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuSb4S7\\n\",\n        \"output\": \" No, EuSb4S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsLu7Se11\\n\",\n        \"output\": \" No, CsLu7Se11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnSn3\\n\",\n        \"output\": \" Yes, ZnSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbH2(IO3)3\\n\",\n        \"output\": \" No, RbH2(IO3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li5Mn3(FeO5)2\\n\",\n        \"output\": \" Yes, Li5Mn3(FeO5)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.65Hg0.35Se1\\n\",\n        \"output\": \" No, Zn0.65Hg0.35Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2PtO3\\n\",\n        \"output\": \" No, Li2PtO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga5Pd13\\n\",\n        \"output\": \" Yes, Ga5Pd13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi0.2Sb1.8Te3\\n\",\n        \"output\": \" No, Bi0.2Sb1.8Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VGa(TeO4)2\\n\",\n        \"output\": \" No, VGa(TeO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnGaPt\\n\",\n        \"output\": \" Yes, MnGaPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuAu\\n\",\n        \"output\": \" Yes, LuAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg(CoS2)2\\n\",\n        \"output\": \" Yes, Mg(CoS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2CaOsO6\\n\",\n        \"output\": \" Yes, Ba2CaOsO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbIn4Rh\\n\",\n        \"output\": \" Yes, YbIn4Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ni2Mo4C\\n\",\n        \"output\": \" Yes, Ni2Mo4C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbPt3\\n\",\n        \"output\": \" Yes, SbPt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" wish\\n\",\n        \"output\": \" wish is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm3(Sb7Te12)2\\n\",\n        \"output\": \" Yes, Sm3(Sb7Te12)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ThPd3\\n\",\n        \"output\": \" Yes, ThPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KAgF3\\n\",\n        \"output\": \" Yes, KAgF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu2MgHg\\n\",\n        \"output\": \" Yes, Lu2MgHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlPS2\\n\",\n        \"output\": \" No, TlPS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PdS2\\n\",\n        \"output\": \" No, PdS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BeTcSe\\n\",\n        \"output\": \" Yes, BeTcSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr2Al\\n\",\n        \"output\": \" Yes, Zr2Al is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScSbPd\\n\",\n        \"output\": \" No, ScSbPd is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiCa2Mg\\n\",\n        \"output\": \" Yes, LiCa2Mg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InPS4\\n\",\n        \"output\": \" No, InPS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnSnO3\\n\",\n        \"output\": \" No, ZnSnO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb23Mg4Cu7\\n\",\n        \"output\": \" Yes, Yb23Mg4Cu7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pt0.97S2\\n\",\n        \"output\": \" No, Pt0.97S2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeNbO4\\n\",\n        \"output\": \" Yes, CeNbO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy7In(CoGe3)4\\n\",\n        \"output\": \" Yes, Dy7In(CoGe3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2AgBiBr6\\n\",\n        \"output\": \" No, Cs2AgBiBr6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta11(CuO6)5\\n\",\n        \"output\": \" No, Ta11(CuO6)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho(SiRu)2\\n\",\n        \"output\": \" Yes, Ho(SiRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmSnRh2\\n\",\n        \"output\": \" Yes, SmSnRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" legal\\n\",\n        \"output\": \" legal is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Ni2(PO4)3\\n\",\n        \"output\": \" Yes, Li4Ni2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrH9(CN2)3\\n\",\n        \"output\": \" Yes, CrH9(CN2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmPd\\n\",\n        \"output\": \" Yes, TmPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Fe(CoO2)4\\n\",\n        \"output\": \" Yes, Li3Fe(CoO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.99Cd0.01Se1\\n\",\n        \"output\": \" No, Zn0.99Cd0.01Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2B(PO4)3\\n\",\n        \"output\": \" No, In2B(PO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsAgCl3\\n\",\n        \"output\": \" Yes, CsAgCl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2Sb\\n\",\n        \"output\": \" Yes, Ce2Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiInSnS4\\n\",\n        \"output\": \" No, LiInSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba4B11O20F\\n\",\n        \"output\": \" No, Ba4B11O20F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.01Te1Pb0.99\\n\",\n        \"output\": \" No, Sn0.01Te1Pb0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" margaret\\n\",\n        \"output\": \" margaret is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho(InS2)3\\n\",\n        \"output\": \" No, Ho(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti2TcNi\\n\",\n        \"output\": \" Yes, Ti2TcNi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce3MnAlS7\\n\",\n        \"output\": \" Yes, Ce3MnAlS7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.05Te1Pb0.95\\n\",\n        \"output\": \" No, Ge0.05Te1Pb0.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm(SiOs)2\\n\",\n        \"output\": \" Yes, Tm(SiOs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbIr2\\n\",\n        \"output\": \" Yes, YbIr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba4InAgSe6\\n\",\n        \"output\": \" No, Ba4InAgSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbMn4In5Se12\\n\",\n        \"output\": \" No, RbMn4In5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca3N2\\n\",\n        \"output\": \" No, Ca3N2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K9Bi13S24\\n\",\n        \"output\": \" No, K9Bi13S24 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Ta2ZnO9\\n\",\n        \"output\": \" No, Ba3Ta2ZnO9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf2Co4P3\\n\",\n        \"output\": \" Yes, Hf2Co4P3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho(CuSe)3\\n\",\n        \"output\": \" No, Ho(CuSe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErNi4Au\\n\",\n        \"output\": \" Yes, ErNi4Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbNiGe2\\n\",\n        \"output\": \" Yes, TbNiGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" B4W\\n\",\n        \"output\": \" Yes, B4W is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na7.36Ga7.24Sn4.78Se24\\n\",\n        \"output\": \" No, Na7.36Ga7.24Sn4.78Se24 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfS3\\n\",\n        \"output\": \" No, HfS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2ReH9\\n\",\n        \"output\": \" No, K2ReH9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KInSnS4\\n\",\n        \"output\": \" No, KInSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu2HgGeSe4\\n\",\n        \"output\": \" Yes, Cu2HgGeSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KSnAuS3\\n\",\n        \"output\": \" No, KSnAuS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Co1Te1.88\\n\",\n        \"output\": \" No, Co1Te1.88 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaSe\\n\",\n        \"output\": \" No, GaSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce3LuSe6\\n\",\n        \"output\": \" No, Ce3LuSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2S\\n\",\n        \"output\": \" No, K2S is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3VOF5\\n\",\n        \"output\": \" Yes, Li3VOF5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu3BWO9\\n\",\n        \"output\": \" Yes, Eu3BWO9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaSn2\\n\",\n        \"output\": \" Yes, NaSn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr(RuO3)2\\n\",\n        \"output\": \" Yes, Sr(RuO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiSiRh2\\n\",\n        \"output\": \" Yes, LiSiRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Si2Hg3S8\\n\",\n        \"output\": \" No, Na2Si2Hg3S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" OsS2\\n\",\n        \"output\": \" No, OsS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" china\\n\",\n        \"output\": \" china is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsNa8(B7O12)3\\n\",\n        \"output\": \" No, CsNa8(B7O12)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hf(VH2)2\\n\",\n        \"output\": \" Yes, Hf(VH2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce(BC)2\\n\",\n        \"output\": \" Yes, Ce(BC)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pt3Pb\\n\",\n        \"output\": \" Yes, Pt3Pb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaV2SeO8\\n\",\n        \"output\": \" No, BaV2SeO8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CoAsSe\\n\",\n        \"output\": \" No, CoAsSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyZrRu2\\n\",\n        \"output\": \" Yes, DyZrRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.8Ga0.2As1\\n\",\n        \"output\": \" No, In0.8Ga0.2As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc3(ReSi2)2\\n\",\n        \"output\": \" Yes, Sc3(ReSi2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" V2(OF)3\\n\",\n        \"output\": \" Yes, V2(OF)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScAgO2\\n\",\n        \"output\": \" No, ScAgO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu2Se3\\n\",\n        \"output\": \" No, Eu2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(ErSe2)2\\n\",\n        \"output\": \" No, Eu(ErSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InS\\n\",\n        \"output\": \" No, InS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VP\\n\",\n        \"output\": \" Yes, VP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErSiPd\\n\",\n        \"output\": \" Yes, ErSiPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Gd3Al7Ag2\\n\",\n        \"output\": \" Yes, Gd3Al7Ag2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb5B(SO4)4\\n\",\n        \"output\": \" No, Rb5B(SO4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf2Tl\\n\",\n        \"output\": \" Yes, Hf2Tl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdTe2\\n\",\n        \"output\": \" No, NdTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgBr\\n\",\n        \"output\": \" No, AgBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmCu4Ag\\n\",\n        \"output\": \" Yes, TmCu4Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyAg\\n\",\n        \"output\": \" Yes, DyAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2Mn9O13\\n\",\n        \"output\": \" Yes, Ca2Mn9O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In6Se7\\n\",\n        \"output\": \" No, In6Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgBiSe2\\n\",\n        \"output\": \" No, AgBiSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnI2\\n\",\n        \"output\": \" No, ZnI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CePd5\\n\",\n        \"output\": \" Yes, CePd5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd(CoSi)2\\n\",\n        \"output\": \" Yes, Nd(CoSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrFeP\\n\",\n        \"output\": \" Yes, CrFeP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al(Ni10B7)2\\n\",\n        \"output\": \" Yes, Al(Ni10B7)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgAgAs\\n\",\n        \"output\": \" Yes, MgAgAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaIn(IO3)4\\n\",\n        \"output\": \" No, NaIn(IO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiAlB4\\n\",\n        \"output\": \" Yes, LiAlB4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho2B4C\\n\",\n        \"output\": \" Yes, Ho2B4C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na(GeP)3\\n\",\n        \"output\": \" No, Na(GeP)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3(ReO5)2\\n\",\n        \"output\": \" Yes, La3(ReO5)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm4MgRh\\n\",\n        \"output\": \" Yes, Sm4MgRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGa2SnSe6\\n\",\n        \"output\": \" No, BaGa2SnSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2VAgS4\\n\",\n        \"output\": \" No, Cs2VAgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Cd(PSe3)2\\n\",\n        \"output\": \" No, Rb2Cd(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbSe\\n\",\n        \"output\": \" No, YbSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Se3\\n\",\n        \"output\": \" No, Bi2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RhSe3\\n\",\n        \"output\": \" No, RhSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmMnGe\\n\",\n        \"output\": \" Yes, TmMnGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg(TiS2)4\\n\",\n        \"output\": \" Yes, Mg(TiS2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaS\\n\",\n        \"output\": \" No, BaS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaPrZn2\\n\",\n        \"output\": \" Yes, CaPrZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyFeSi\\n\",\n        \"output\": \" Yes, DyFeSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si(Bi3O5)4\\n\",\n        \"output\": \" No, Si(Bi3O5)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TaNiB2\\n\",\n        \"output\": \" Yes, TaNiB2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoZnRh2\\n\",\n        \"output\": \" Yes, HoZnRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2NbCuS4\\n\",\n        \"output\": \" No, Rb2NbCuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgP15\\n\",\n        \"output\": \" No, AgP15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.01Ga0.99Sb0.99Te0.01\\n\",\n        \"output\": \" No, Zn0.01Ga0.99Sb0.99Te0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ni4(PO4)3\\n\",\n        \"output\": \" Yes, Ni4(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2CuWO6\\n\",\n        \"output\": \" Yes, Mg2CuWO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn2GaW\\n\",\n        \"output\": \" Yes, Mn2GaW is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al2FeNi\\n\",\n        \"output\": \" Yes, Al2FeNi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al2Se3\\n\",\n        \"output\": \" No, Al2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Re3F\\n\",\n        \"output\": \" Yes, Re3F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" grass\\n\",\n        \"output\": \" grass is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnO2\\n\",\n        \"output\": \" No, MnO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc2MnC\\n\",\n        \"output\": \" Yes, Sc2MnC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K8N3O\\n\",\n        \"output\": \" Yes, K8N3O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2OF3\\n\",\n        \"output\": \" Yes, Mn2OF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2AgBiCl6\\n\",\n        \"output\": \" No, Cs2AgBiCl6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiAlGe\\n\",\n        \"output\": \" Yes, LiAlGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrCd\\n\",\n        \"output\": \" Yes, SrCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si3N4\\n\",\n        \"output\": \" No, Si3N4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaCdAu\\n\",\n        \"output\": \" Yes, LaCdAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.01Ga0.99P0.99S0.01\\n\",\n        \"output\": \" No, Zn0.01Ga0.99P0.99S0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu2TlCd\\n\",\n        \"output\": \" Yes, Lu2TlCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YMgGa\\n\",\n        \"output\": \" Yes, YMgGa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VP4\\n\",\n        \"output\": \" Yes, VP4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Te0.6Se0.4\\n\",\n        \"output\": \" No, Te0.6Se0.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgAsS2\\n\",\n        \"output\": \" No, AgAsS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2Zn3(SeO3)4\\n\",\n        \"output\": \" No, Cs2Zn3(SeO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn3Cu10(TeO6)6\\n\",\n        \"output\": \" Yes, Zn3Cu10(TeO6)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1.002Sb0.998Se0.006\\n\",\n        \"output\": \" No, Ga1.002Sb0.998Se0.006 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScZn3\\n\",\n        \"output\": \" Yes, ScZn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Gd2Ti3O10\\n\",\n        \"output\": \" No, K2Gd2Ti3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KHg11\\n\",\n        \"output\": \" Yes, KHg11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2NaNiF6\\n\",\n        \"output\": \" Yes, Rb2NaNiF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgNiSb\\n\",\n        \"output\": \" Yes, MgNiSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SiP2\\n\",\n        \"output\": \" No, SiP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCu2AsS3\\n\",\n        \"output\": \" No, CsCu2AsS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2S3\\n\",\n        \"output\": \" No, Ga2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr2CuTe4\\n\",\n        \"output\": \" Yes, Cr2CuTe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaInTe2\\n\",\n        \"output\": \" No, NaInTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KY(TeO3)2\\n\",\n        \"output\": \" No, KY(TeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlInGeS4\\n\",\n        \"output\": \" No, TlInGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd(CoGe)2\\n\",\n        \"output\": \" Yes, Nd(CoGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrCuSO\\n\",\n        \"output\": \" No, PrCuSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Be3Sb2\\n\",\n        \"output\": \" No, Be3Sb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.3Ga0.7P0.7S0.3\\n\",\n        \"output\": \" No, Zn0.3Ga0.7P0.7S0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr2Se3\\n\",\n        \"output\": \" No, Pr2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TaF3\\n\",\n        \"output\": \" Yes, TaF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdS\\n\",\n        \"output\": \" No, CdS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsZn4In5Te12\\n\",\n        \"output\": \" No, CsZn4In5Te12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgSi7Ir3\\n\",\n        \"output\": \" Yes, MgSi7Ir3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga5Ge(PbS3)4\\n\",\n        \"output\": \" No, Ga5Ge(PbS3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlCuCl3\\n\",\n        \"output\": \" No, TlCuCl3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsLu7S11\\n\",\n        \"output\": \" No, CsLu7S11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3(CuO2)2\\n\",\n        \"output\": \" Yes, Li3(CuO2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgGeO3\\n\",\n        \"output\": \" Yes, AgGeO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu4W(SCl)4\\n\",\n        \"output\": \" Yes, Cu4W(SCl)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdO2\\n\",\n        \"output\": \" Yes, GdO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaSi\\n\",\n        \"output\": \" Yes, LaSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaLaS3\\n\",\n        \"output\": \" No, NaLaS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K10Fe4Sn4S17\\n\",\n        \"output\": \" No, K10Fe4Sn4S17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Mn5Cu3O16\\n\",\n        \"output\": \" Yes, Li4Mn5Cu3O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.4Ga0.6As0.4P0.6\\n\",\n        \"output\": \" No, In0.4Ga0.6As0.4P0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbInIr\\n\",\n        \"output\": \" Yes, TbInIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PtSe2\\n\",\n        \"output\": \" No, PtSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti2RePd\\n\",\n        \"output\": \" Yes, Ti2RePd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr3Cd\\n\",\n        \"output\": \" Yes, Pr3Cd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd4As2I3\\n\",\n        \"output\": \" No, Cd4As2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3PS4\\n\",\n        \"output\": \" No, Li3PS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi12Rh12O41\\n\",\n        \"output\": \" Yes, Bi12Rh12O41 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge5(Te4As)2\\n\",\n        \"output\": \" Yes, Ge5(Te4As)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsYbMnSe3\\n\",\n        \"output\": \" No, CsYbMnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsK(PSe4)2\\n\",\n        \"output\": \" No, CsK(PSe4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" V3SiNi2\\n\",\n        \"output\": \" Yes, V3SiNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Si0.03Ge0.97\\n\",\n        \"output\": \" No, Si0.03Ge0.97 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb2EuSe4\\n\",\n        \"output\": \" No, Tb2EuSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiBi3(ClO2)2\\n\",\n        \"output\": \" No, LiBi3(ClO2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce(SiPd)2\\n\",\n        \"output\": \" Yes, Ce(SiPd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pd16S7\\n\",\n        \"output\": \" Yes, Pd16S7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm3Sc\\n\",\n        \"output\": \" Yes, Sm3Sc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiTlPS5\\n\",\n        \"output\": \" No, TiTlPS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaInPt\\n\",\n        \"output\": \" Yes, CaInPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" scene\\n\",\n        \"output\": \" scene is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ErTe\\n\",\n        \"output\": \" No, ErTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Er2(PS4)4\\n\",\n        \"output\": \" No, Ba3Er2(PS4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Co3CuO8\\n\",\n        \"output\": \" Yes, Li4Co3CuO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb2Pt\\n\",\n        \"output\": \" No, Sb2Pt is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2Al2Co15\\n\",\n        \"output\": \" Yes, Ce2Al2Co15 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiIO3\\n\",\n        \"output\": \" No, LiIO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaSnO3\\n\",\n        \"output\": \" No, CaSnO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" tuna\\n\",\n        \"output\": \" tuna is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cr2SbTe\\n\",\n        \"output\": \" Yes, Cr2SbTe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrSiPd\\n\",\n        \"output\": \" Yes, SrSiPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3Nb2Se9\\n\",\n        \"output\": \" No, Ba3Nb2Se9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HgPS3\\n\",\n        \"output\": \" No, HgPS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U2(Co7B2)3\\n\",\n        \"output\": \" Yes, U2(Co7B2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.4Te1Pb0.6\\n\",\n        \"output\": \" No, Ge0.4Te1Pb0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2Ga2GeS8\\n\",\n        \"output\": \" No, La2Ga2GeS8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba14Na8CaN6\\n\",\n        \"output\": \" Yes, Ba14Na8CaN6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2HgS4\\n\",\n        \"output\": \" No, In2HgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbIn2Ni\\n\",\n        \"output\": \" Yes, TbIn2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1Sb0.95As0.05\\n\",\n        \"output\": \" No, Ga1Sb0.95As0.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al7(CN)3\\n\",\n        \"output\": \" Yes, Al7(CN)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InAgTe2\\n\",\n        \"output\": \" No, InAgTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4.5Fe0.5Te1O6\\n\",\n        \"output\": \" No, Li4.5Fe0.5Te1O6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsCaO3\\n\",\n        \"output\": \" Yes, CsCaO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca4Bi6O13\\n\",\n        \"output\": \" No, Ca4Bi6O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfZnNi2\\n\",\n        \"output\": \" Yes, HfZnNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu2Mn12P7\\n\",\n        \"output\": \" Yes, Lu2Mn12P7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgCo2(PO5)2\\n\",\n        \"output\": \" Yes, MgCo2(PO5)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba5Ge3\\n\",\n        \"output\": \" Yes, Ba5Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3FeTe4O11\\n\",\n        \"output\": \" No, Li3FeTe4O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.35Hg0.65Te1\\n\",\n        \"output\": \" No, Cd0.35Hg0.65Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al0.6Ga0.4P1\\n\",\n        \"output\": \" No, Al0.6Ga0.4P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pb1Se0.99S0.01\\n\",\n        \"output\": \" No, Pb1Se0.99S0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1Sb0.5As0.5\\n\",\n        \"output\": \" No, In1Sb0.5As0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Th(Al5Fe)2\\n\",\n        \"output\": \" Yes, Th(Al5Fe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr7P4\\n\",\n        \"output\": \" Yes, Zr7P4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KSbSe2\\n\",\n        \"output\": \" No, KSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr2YReO6\\n\",\n        \"output\": \" Yes, Sr2YReO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.7Ge0.3\\n\",\n        \"output\": \" No, Si0.7Ge0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K4Al4Si19\\n\",\n        \"output\": \" No, K4Al4Si19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu3Sn\\n\",\n        \"output\": \" Yes, Eu3Sn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Al2B2O7\\n\",\n        \"output\": \" No, Cs2Al2B2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoNiGe\\n\",\n        \"output\": \" Yes, HoNiGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiCu2(CO3)2\\n\",\n        \"output\": \" Yes, LiCu2(CO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La8Sb2S15\\n\",\n        \"output\": \" No, La8Sb2S15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HgPt3\\n\",\n        \"output\": \" Yes, HgPt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" As2S3\\n\",\n        \"output\": \" No, As2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmMgCd2\\n\",\n        \"output\": \" Yes, TmMgCd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdSn2\\n\",\n        \"output\": \" Yes, NdSn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiAlRh2\\n\",\n        \"output\": \" Yes, LiAlRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfOs2\\n\",\n        \"output\": \" Yes, HfOs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdZn2Ag\\n\",\n        \"output\": \" Yes, NdZn2Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsLaHgSe3\\n\",\n        \"output\": \" No, CsLaHgSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce(PPt2)2\\n\",\n        \"output\": \" Yes, Ce(PPt2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce2SiSeO4\\n\",\n        \"output\": \" Yes, Ce2SiSeO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ni2Mo4N\\n\",\n        \"output\": \" Yes, Ni2Mo4N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Ni(SbO3)4\\n\",\n        \"output\": \" Yes, Li3Ni(SbO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr2In5Ni\\n\",\n        \"output\": \" Yes, Zr2In5Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoMg2\\n\",\n        \"output\": \" Yes, HoMg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2O5\\n\",\n        \"output\": \" No, V2O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2NaCoF6\\n\",\n        \"output\": \" Yes, Cs2NaCoF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdSnAs2\\n\",\n        \"output\": \" No, CdSnAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaZnSO\\n\",\n        \"output\": \" No, BaZnSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba4Ga5CuS12\\n\",\n        \"output\": \" No, Ba4Ga5CuS12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HgOsPb2\\n\",\n        \"output\": \" Yes, HgOsPb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KCeSe4\\n\",\n        \"output\": \" No, KCeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlCuS2\\n\",\n        \"output\": \" No, AlCuS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb(Fe2Ge)2\\n\",\n        \"output\": \" Yes, Yb(Fe2Ge)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AsSI\\n\",\n        \"output\": \" No, AsSI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.07Ge0.93\\n\",\n        \"output\": \" No, Si0.07Ge0.93 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr2Be2B2O7\\n\",\n        \"output\": \" No, Sr2Be2B2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ni7(P2O7)4\\n\",\n        \"output\": \" Yes, Ni7(P2O7)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2TlAg\\n\",\n        \"output\": \" Yes, Li2TlAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2S3\\n\",\n        \"output\": \" No, In2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V4ZnO8\\n\",\n        \"output\": \" Yes, V4ZnO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GeP\\n\",\n        \"output\": \" No, GeP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsB3O5\\n\",\n        \"output\": \" No, CsB3O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgGeN2\\n\",\n        \"output\": \" No, MgGeN2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd3P2\\n\",\n        \"output\": \" No, Cd3P2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NiAsO3\\n\",\n        \"output\": \" Yes, NiAsO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs1.43Cd1.43Bi2.57S6\\n\",\n        \"output\": \" No, Cs1.43Cd1.43Bi2.57S6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" nail\\n\",\n        \"output\": \" nail is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2Hg(ICl)2\\n\",\n        \"output\": \" No, Cs2Hg(ICl)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd2Te3\\n\",\n        \"output\": \" No, Nd2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbYHg2\\n\",\n        \"output\": \" Yes, TbYHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr(FeSe2)2\\n\",\n        \"output\": \" Yes, Cr(FeSe2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiSiPd2\\n\",\n        \"output\": \" Yes, LiSiPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3Ho2(PS4)4\\n\",\n        \"output\": \" No, Ba3Ho2(PS4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs4Ge5(PbS4)4\\n\",\n        \"output\": \" No, Cs4Ge5(PbS4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiMoIO6\\n\",\n        \"output\": \" No, LiMoIO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaB6\\n\",\n        \"output\": \" No, CaB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgTl\\n\",\n        \"output\": \" Yes, MgTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf7P4\\n\",\n        \"output\": \" Yes, Hf7P4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu(HoSe2)2\\n\",\n        \"output\": \" No, Eu(HoSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.07Te1Pb0.93\\n\",\n        \"output\": \" No, In0.07Te1Pb0.93 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al9Rh2\\n\",\n        \"output\": \" Yes, Al9Rh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaZnGeSe4\\n\",\n        \"output\": \" No, BaZnGeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScPPt\\n\",\n        \"output\": \" Yes, ScPPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te0.01Pb1Se0.99\\n\",\n        \"output\": \" No, Te0.01Pb1Se0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KLiCO3\\n\",\n        \"output\": \" No, KLiCO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TaPt3\\n\",\n        \"output\": \" Yes, TaPt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K4Ga4Si19\\n\",\n        \"output\": \" No, K4Ga4Si19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrSm3\\n\",\n        \"output\": \" Yes, PrSm3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InSnAsSe\\n\",\n        \"output\": \" No, InSnAsSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnTcOs\\n\",\n        \"output\": \" Yes, MnTcOs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoCd3\\n\",\n        \"output\": \" Yes, HoCd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaH2\\n\",\n        \"output\": \" Yes, LaH2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuAlO3\\n\",\n        \"output\": \" Yes, EuAlO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2Hg3Se4\\n\",\n        \"output\": \" No, Tl2Hg3Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca3La2(SnS4)3\\n\",\n        \"output\": \" No, Ca3La2(SnS4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm2MgRu\\n\",\n        \"output\": \" Yes, Tm2MgRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2Rh7\\n\",\n        \"output\": \" Yes, La2Rh7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbIn5S6\\n\",\n        \"output\": \" No, RbIn5S6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(GaS2)2\\n\",\n        \"output\": \" No, Eu(GaS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li8TiNi7O16\\n\",\n        \"output\": \" Yes, Li8TiNi7O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn3V2(SiO4)3\\n\",\n        \"output\": \" Yes, Mn3V2(SiO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeIr5\\n\",\n        \"output\": \" Yes, CeIr5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YNi4B\\n\",\n        \"output\": \" Yes, YNi4B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GdTe\\n\",\n        \"output\": \" No, GdTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrSnP\\n\",\n        \"output\": \" Yes, SrSnP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiOs3\\n\",\n        \"output\": \" Yes, TiOs3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba(BRh)2\\n\",\n        \"output\": \" Yes, Ba(BRh)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu2Ge(BO4)2\\n\",\n        \"output\": \" Yes, Eu2Ge(BO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2Mn3(SbS3)4\\n\",\n        \"output\": \" No, Sm2Mn3(SbS3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PbCl2\\n\",\n        \"output\": \" No, PbCl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu7(TePd)2\\n\",\n        \"output\": \" Yes, Lu7(TePd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Au3S\\n\",\n        \"output\": \" Yes, Au3S is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TePd\\n\",\n        \"output\": \" Yes, TePd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn3Cd\\n\",\n        \"output\": \" Yes, Zn3Cd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VB2\\n\",\n        \"output\": \" Yes, VB2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbCe2CuS5\\n\",\n        \"output\": \" No, YbCe2CuS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SeS\\n\",\n        \"output\": \" No, SeS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta4FeTe4\\n\",\n        \"output\": \" Yes, Ta4FeTe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy2ZnIn\\n\",\n        \"output\": \" Yes, Dy2ZnIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NbPt2\\n\",\n        \"output\": \" Yes, NbPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrRhF6\\n\",\n        \"output\": \" Yes, SrRhF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnIrO3\\n\",\n        \"output\": \" Yes, ZnIrO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Ti3O7\\n\",\n        \"output\": \" No, Na2Ti3O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn2WN2\\n\",\n        \"output\": \" Yes, Zn2WN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti2CuS4\\n\",\n        \"output\": \" Yes, Ti2CuS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbHg3\\n\",\n        \"output\": \" Yes, RbHg3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InCuS2\\n\",\n        \"output\": \" No, InCuS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrPd2\\n\",\n        \"output\": \" Yes, ZrPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd2S3\\n\",\n        \"output\": \" No, Nd2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2DyCu3O7\\n\",\n        \"output\": \" Yes, Ba2DyCu3O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ThSi\\n\",\n        \"output\": \" Yes, ThSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag2P2PbO7\\n\",\n        \"output\": \" Yes, Ag2P2PbO7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2FeGe3Se8\\n\",\n        \"output\": \" No, K2FeGe3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.2Hg0.8Se1\\n\",\n        \"output\": \" No, Cd0.2Hg0.8Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrErIn2\\n\",\n        \"output\": \" Yes, PrErIn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" winter\\n\",\n        \"output\": \" winter is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl2GeTe3\\n\",\n        \"output\": \" No, Tl2GeTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3BiSb\\n\",\n        \"output\": \" Yes, Ca3BiSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm(MnGe)6\\n\",\n        \"output\": \" Yes, Tm(MnGe)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.65Cu0.35S2.65\\n\",\n        \"output\": \" No, Ga1.65Cu0.35S2.65 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2HgS5\\n\",\n        \"output\": \" No, Ba2HgS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaTi5Se8\\n\",\n        \"output\": \" Yes, NaTi5Se8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbTlSe2\\n\",\n        \"output\": \" Yes, YbTlSe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdGa2Ni\\n\",\n        \"output\": \" Yes, NdGa2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NbCu3Se4\\n\",\n        \"output\": \" No, NbCu3Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn4Sb3\\n\",\n        \"output\": \" No, Zn4Sb3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In2FeSe4\\n\",\n        \"output\": \" No, In2FeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K10Zn4Sn4S17\\n\",\n        \"output\": \" No, K10Zn4Sn4S17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaB15\\n\",\n        \"output\": \" No, NaB15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgPt3\\n\",\n        \"output\": \" Yes, AgPt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiPm2Ir\\n\",\n        \"output\": \" Yes, LiPm2Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrBPt4\\n\",\n        \"output\": \" Yes, PrBPt4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdSmHg2\\n\",\n        \"output\": \" Yes, NdSmHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" guarantee\\n\",\n        \"output\": \" guarantee is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsSb(SO4)2\\n\",\n        \"output\": \" No, CsSb(SO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InSiIr\\n\",\n        \"output\": \" Yes, InSiIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc5NCl8\\n\",\n        \"output\": \" Yes, Sc5NCl8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.13Pb0.87Se1\\n\",\n        \"output\": \" No, Sn0.13Pb0.87Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti2CoS4\\n\",\n        \"output\": \" Yes, Ti2CoS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Cr3NiO8\\n\",\n        \"output\": \" Yes, Li4Cr3NiO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbSnTe2\\n\",\n        \"output\": \" No, YbSnTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta2Nb3O12\\n\",\n        \"output\": \" Yes, Ta2Nb3O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2Se2O7\\n\",\n        \"output\": \" No, In2Se2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaZr2TiF11\\n\",\n        \"output\": \" Yes, NaZr2TiF11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KHg2\\n\",\n        \"output\": \" Yes, KHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Te\\n\",\n        \"output\": \" No, K2Te is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La3LuSe6\\n\",\n        \"output\": \" No, La3LuSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnSbPd\\n\",\n        \"output\": \" Yes, MnSbPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeAlO3\\n\",\n        \"output\": \" Yes, CeAlO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr5Sb3\\n\",\n        \"output\": \" Yes, Zr5Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgF2\\n\",\n        \"output\": \" No, MgF2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TaW3\\n\",\n        \"output\": \" Yes, TaW3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2CdSnS4\\n\",\n        \"output\": \" No, Li2CdSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdCrGe3\\n\",\n        \"output\": \" Yes, NdCrGe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnPSe3\\n\",\n        \"output\": \" No, MnPSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BePd3\\n\",\n        \"output\": \" Yes, BePd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmBiW2O9\\n\",\n        \"output\": \" No, SmBiW2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" FeAsSe\\n\",\n        \"output\": \" No, FeAsSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr4Te7\\n\",\n        \"output\": \" No, Pr4Te7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrRe2\\n\",\n        \"output\": \" Yes, ZrRe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Te2Se\\n\",\n        \"output\": \" No, Bi2Te2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCl\\n\",\n        \"output\": \" No, CsCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2Sn\\n\",\n        \"output\": \" No, Mg2Sn is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.01Ga0.99As1\\n\",\n        \"output\": \" No, In0.01Ga0.99As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn1Se0.75S0.25\\n\",\n        \"output\": \" No, Sn1Se0.75S0.25 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe2O2F3\\n\",\n        \"output\": \" Yes, Fe2O2F3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1As0.01P0.99\\n\",\n        \"output\": \" No, Ga1As0.01P0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho2Pd2Pb\\n\",\n        \"output\": \" Yes, Ho2Pd2Pb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ThU8O18\\n\",\n        \"output\": \" Yes, ThU8O18 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsCu(SbS2)2\\n\",\n        \"output\": \" No, CsCu(SbS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmNi2B2C\\n\",\n        \"output\": \" Yes, SmNi2B2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiPr2Ru\\n\",\n        \"output\": \" Yes, LiPr2Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbCu(SbS2)2\\n\",\n        \"output\": \" No, RbCu(SbS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsGa(SnSe3)2\\n\",\n        \"output\": \" No, CsGa(SnSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdAsPd5\\n\",\n        \"output\": \" Yes, CdAsPd5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuCd4B3O10\\n\",\n        \"output\": \" No, LuCd4B3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag7NO11\\n\",\n        \"output\": \" Yes, Ag7NO11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1Sb0.01As0.99\\n\",\n        \"output\": \" No, In1Sb0.01As0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu3Pd\\n\",\n        \"output\": \" Yes, Cu3Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiHfPd2\\n\",\n        \"output\": \" Yes, LiHfPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SiAs2\\n\",\n        \"output\": \" No, SiAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2In2GeSe6\\n\",\n        \"output\": \" No, Na2In2GeSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr3Ni(PO4)6\\n\",\n        \"output\": \" Yes, Cr3Ni(PO4)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb(GaS2)2\\n\",\n        \"output\": \" No, Yb(GaS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuNi(CN)4\\n\",\n        \"output\": \" No, CuNi(CN)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" packet\\n\",\n        \"output\": \" packet is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiMn2(PO4)2\\n\",\n        \"output\": \" Yes, LiMn2(PO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Co(NiO2)4\\n\",\n        \"output\": \" Yes, Li3Co(NiO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrV13O18\\n\",\n        \"output\": \" Yes, SrV13O18 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Ti(AgS2)2\\n\",\n        \"output\": \" No, Rb2Ti(AgS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaMgSn\\n\",\n        \"output\": \" Yes, CaMgSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AsPPt\\n\",\n        \"output\": \" No, AsPPt is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiInTe2\\n\",\n        \"output\": \" No, LiInTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Co7Re17O48\\n\",\n        \"output\": \" Yes, Co7Re17O48 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg2AgIr\\n\",\n        \"output\": \" Yes, Mg2AgIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdCu2GeS4\\n\",\n        \"output\": \" No, CdCu2GeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgSiN2\\n\",\n        \"output\": \" No, MgSiN2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" carnation\\n\",\n        \"output\": \" carnation is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CrPbO4\\n\",\n        \"output\": \" No, CrPbO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" male\\n\",\n        \"output\": \" male is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3N2\\n\",\n        \"output\": \" Yes, Ba3N2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgSc\\n\",\n        \"output\": \" Yes, MgSc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca3Bi(PO4)3\\n\",\n        \"output\": \" No, Ca3Bi(PO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmThRu2\\n\",\n        \"output\": \" Yes, TmThRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd2Fe14B\\n\",\n        \"output\": \" Yes, Nd2Fe14B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" clipper\\n\",\n        \"output\": \" clipper is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti5(B6O13)2\\n\",\n        \"output\": \" Yes, Ti5(B6O13)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuBiPbS3\\n\",\n        \"output\": \" No, CuBiPbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Fe4H15(IO8)3\\n\",\n        \"output\": \" No, Fe4H15(IO8)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd0.02In0.98Te0.02As0.98\\n\",\n        \"output\": \" No, Cd0.02In0.98Te0.02As0.98 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlN\\n\",\n        \"output\": \" No, AlN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al0.4In0.6P1\\n\",\n        \"output\": \" No, Al0.4In0.6P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlGaSe2\\n\",\n        \"output\": \" No, TlGaSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaCaB2O5\\n\",\n        \"output\": \" No, BaCaB2O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce(InS2)3\\n\",\n        \"output\": \" No, Ce(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3V4NiO12\\n\",\n        \"output\": \" Yes, Li3V4NiO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Fe7(OF7)2\\n\",\n        \"output\": \" Yes, Li4Fe7(OF7)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li5Cr2Ni5O12\\n\",\n        \"output\": \" Yes, Li5Cr2Ni5O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr3(AlSn)2\\n\",\n        \"output\": \" Yes, Sr3(AlSn)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiPO4\\n\",\n        \"output\": \" No, BiPO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.2Ge0.8\\n\",\n        \"output\": \" No, Si0.2Ge0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb6O\\n\",\n        \"output\": \" Yes, Rb6O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Ti2(PO4)3\\n\",\n        \"output\": \" Yes, Li3Ti2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In(PSe2)2\\n\",\n        \"output\": \" No, In(PSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Fe3NiO8\\n\",\n        \"output\": \" Yes, Li2Fe3NiO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2GaBiS5\\n\",\n        \"output\": \" No, Ba2GaBiS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe4Si2Sn7O16\\n\",\n        \"output\": \" Yes, Fe4Si2Sn7O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" soup\\n\",\n        \"output\": \" soup is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr4V2(Se2O7)3\\n\",\n        \"output\": \" No, Sr4V2(Se2O7)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2B4O7\\n\",\n        \"output\": \" No, Li2B4O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlVCo2\\n\",\n        \"output\": \" Yes, AlVCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiPm2Si\\n\",\n        \"output\": \" Yes, LiPm2Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc3Fe2Si3\\n\",\n        \"output\": \" Yes, Sc3Fe2Si3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2Ti2O7\\n\",\n        \"output\": \" Yes, Ce2Ti2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2DyInSe5\\n\",\n        \"output\": \" No, Ba2DyInSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InCuGeSe4\\n\",\n        \"output\": \" No, InCuGeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf2Hg\\n\",\n        \"output\": \" Yes, Hf2Hg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2ZnS4\\n\",\n        \"output\": \" Yes, Ti2ZnS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuIr\\n\",\n        \"output\": \" Yes, LuIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaCaSn3\\n\",\n        \"output\": \" Yes, BaCaSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr(GaAu)2\\n\",\n        \"output\": \" Yes, Sr(GaAu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2Se\\n\",\n        \"output\": \" No, Na2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr5Sn3\\n\",\n        \"output\": \" Yes, Sr5Sn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te2MoWS2\\n\",\n        \"output\": \" Yes, Te2MoWS2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2GeSe5\\n\",\n        \"output\": \" No, Ce2GeSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U4Re7Si6\\n\",\n        \"output\": \" Yes, U4Re7Si6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnHg3(SCl2)2\\n\",\n        \"output\": \" No, ZnHg3(SCl2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiHf2Ir\\n\",\n        \"output\": \" Yes, LiHf2Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaGaS3\\n\",\n        \"output\": \" No, LaGaS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HgTeI\\n\",\n        \"output\": \" No, HgTeI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nb3In\\n\",\n        \"output\": \" Yes, Nb3In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2Li2Nb3O10\\n\",\n        \"output\": \" Yes, Sr2Li2Nb3O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaO\\n\",\n        \"output\": \" No, BaO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2Mo15S19\\n\",\n        \"output\": \" Yes, Cs2Mo15S19 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiGa(GeSe3)2\\n\",\n        \"output\": \" No, LiGa(GeSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.5Ga0.5As0.5Se0.5\\n\",\n        \"output\": \" No, Zn0.5Ga0.5As0.5Se0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn3WO6\\n\",\n        \"output\": \" No, Sn3WO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr4Sb3\\n\",\n        \"output\": \" Yes, Pr4Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.05Te0.95Pb0.95S0.05\\n\",\n        \"output\": \" No, Ge0.05Te0.95Pb0.95S0.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1.2Cu0.8Se2.2\\n\",\n        \"output\": \" No, Ga1.2Cu0.8Se2.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn0.07Pb0.93Se1\\n\",\n        \"output\": \" No, Sn0.07Pb0.93Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmAg\\n\",\n        \"output\": \" Yes, SmAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.9Hg0.1Se1\\n\",\n        \"output\": \" No, Cd0.9Hg0.1Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3SbN\\n\",\n        \"output\": \" Yes, Ca3SbN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BeTe\\n\",\n        \"output\": \" No, BeTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KH(CN2)3\\n\",\n        \"output\": \" Yes, KH(CN2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgSbTe2\\n\",\n        \"output\": \" No, AgSbTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiMg2Ag\\n\",\n        \"output\": \" Yes, LiMg2Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuS\\n\",\n        \"output\": \" No, EuS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2S\\n\",\n        \"output\": \" No, Na2S is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf5Si4\\n\",\n        \"output\": \" Yes, Hf5Si4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K10Zn4Ge4S17\\n\",\n        \"output\": \" No, K10Zn4Ge4S17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" P4Ru\\n\",\n        \"output\": \" No, P4Ru is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm(CuTe)3\\n\",\n        \"output\": \" No, Tm(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BiPd\\n\",\n        \"output\": \" Yes, BiPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga2SiPbSe6\\n\",\n        \"output\": \" No, Ga2SiPbSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2TiCoO6\\n\",\n        \"output\": \" No, La2TiCoO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr(CoP)2\\n\",\n        \"output\": \" Yes, Sr(CoP)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CoAsS\\n\",\n        \"output\": \" No, CoAsS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuBiW2O9\\n\",\n        \"output\": \" No, EuBiW2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" chest\\n\",\n        \"output\": \" chest is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsYbZnSe3\\n\",\n        \"output\": \" No, CsYbZnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdF3\\n\",\n        \"output\": \" No, NdF3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YZn5\\n\",\n        \"output\": \" Yes, YZn5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y6Zn(SiS7)2\\n\",\n        \"output\": \" No, Y6Zn(SiS7)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeRh\\n\",\n        \"output\": \" Yes, CeRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlAs\\n\",\n        \"output\": \" Yes, AlAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Te0.03Se2.97\\n\",\n        \"output\": \" No, Bi2Te0.03Se2.97 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Gd4GaSbS9\\n\",\n        \"output\": \" No, Gd4GaSbS9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiCo7O7F\\n\",\n        \"output\": \" Yes, LiCo7O7F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KAsSe2\\n\",\n        \"output\": \" No, KAsSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La(SiRu)2\\n\",\n        \"output\": \" Yes, La(SiRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.7Ga0.3As0.3Se0.7\\n\",\n        \"output\": \" No, Zn0.7Ga0.3As0.3Se0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiBi25O39\\n\",\n        \"output\": \" No, TiBi25O39 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.9Ga0.1As0.9P0.1\\n\",\n        \"output\": \" No, In0.9Ga0.1As0.9P0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li5Co2Ni3O10\\n\",\n        \"output\": \" Yes, Li5Co2Ni3O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsSbS2\\n\",\n        \"output\": \" No, CsSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" No, Cu0.5Ge1Pb1.75S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuSeO3\\n\",\n        \"output\": \" Yes, CuSeO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaI\\n\",\n        \"output\": \" No, NaI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiV3O4\\n\",\n        \"output\": \" Yes, LiV3O4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmGe\\n\",\n        \"output\": \" Yes, TmGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y3(Fe31B7)2\\n\",\n        \"output\": \" Yes, Y3(Fe31B7)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2As2Cl2O5\\n\",\n        \"output\": \" No, In2As2Cl2O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrNi2(PO4)2\\n\",\n        \"output\": \" Yes, SrNi2(PO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1As0.6P0.4\\n\",\n        \"output\": \" No, Ga1As0.6P0.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.25Te1Pb0.75\\n\",\n        \"output\": \" No, Sn0.25Te1Pb0.75 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca(AgGe)2\\n\",\n        \"output\": \" Yes, Ca(AgGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2V2ZnO8\\n\",\n        \"output\": \" No, Ba2V2ZnO8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InAgS2\\n\",\n        \"output\": \" No, InAgS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InHgW2\\n\",\n        \"output\": \" Yes, InHgW2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce(SiNi)2\\n\",\n        \"output\": \" Yes, Ce(SiNi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGe4(IrSe3)2\\n\",\n        \"output\": \" No, BaGe4(IrSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba4Sm2Cu2O9\\n\",\n        \"output\": \" Yes, Ba4Sm2Cu2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn3(BO3)2\\n\",\n        \"output\": \" No, Zn3(BO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La5SmS8\\n\",\n        \"output\": \" Yes, La5SmS8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" InAg3\\n\",\n        \"output\": \" Yes, InAg3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy1Te1.7\\n\",\n        \"output\": \" No, Dy1Te1.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe6O7F5\\n\",\n        \"output\": \" Yes, Fe6O7F5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmCuSe2\\n\",\n        \"output\": \" No, SmCuSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmErMg2\\n\",\n        \"output\": \" Yes, SmErMg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmLuTl2\\n\",\n        \"output\": \" Yes, SmLuTl2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.6Ga0.4As1\\n\",\n        \"output\": \" No, Al0.6Ga0.4As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La4In5S13\\n\",\n        \"output\": \" Yes, La4In5S13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd4Mg3Co2\\n\",\n        \"output\": \" Yes, Nd4Mg3Co2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Th2Fe7\\n\",\n        \"output\": \" Yes, Th2Fe7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KV4Ag11O16\\n\",\n        \"output\": \" No, KV4Ag11O16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3InS4Cl\\n\",\n        \"output\": \" No, Ba3InS4Cl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiPm2Ga\\n\",\n        \"output\": \" Yes, LiPm2Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3Mg0.5Sn1S14\\n\",\n        \"output\": \" No, La3Mg0.5Sn1S14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiCr3(PO4)6\\n\",\n        \"output\": \" Yes, TiCr3(PO4)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbTl\\n\",\n        \"output\": \" Yes, TbTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiCoS2\\n\",\n        \"output\": \" Yes, LiCoS2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyN\\n\",\n        \"output\": \" No, DyN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca3(GaPt)2\\n\",\n        \"output\": \" Yes, Ca3(GaPt)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaGaPt\\n\",\n        \"output\": \" Yes, TaGaPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1As0.4P0.6\\n\",\n        \"output\": \" No, Ga1As0.4P0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgBiS2\\n\",\n        \"output\": \" No, AgBiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy2Te3\\n\",\n        \"output\": \" No, Dy2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hg3PS3\\n\",\n        \"output\": \" No, Hg3PS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiSbSe2\\n\",\n        \"output\": \" No, LiSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaEuO2\\n\",\n        \"output\": \" Yes, CaEuO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrTe\\n\",\n        \"output\": \" Yes, ZrTe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnFeCoGe\\n\",\n        \"output\": \" Yes, MnFeCoGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" sort\\n\",\n        \"output\": \" sort is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K5In3P6Se19\\n\",\n        \"output\": \" No, K5In3P6Se19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrSmO2\\n\",\n        \"output\": \" Yes, PrSmO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd(SiIr)2\\n\",\n        \"output\": \" Yes, Nd(SiIr)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr2InGe2\\n\",\n        \"output\": \" Yes, Pr2InGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrW2\\n\",\n        \"output\": \" Yes, ZrW2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2Te3\\n\",\n        \"output\": \" No, Ga2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2GeN2\\n\",\n        \"output\": \" Yes, Ca2GeN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb2MgS4\\n\",\n        \"output\": \" Yes, Yb2MgS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" german\\n\",\n        \"output\": \" german is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.15Te1Pb0.85\\n\",\n        \"output\": \" No, Ge0.15Te1Pb0.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InSe\\n\",\n        \"output\": \" No, InSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Hg3(GeS4)2\\n\",\n        \"output\": \" No, Na2Hg3(GeS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Fe9Co7\\n\",\n        \"output\": \" Yes, Fe9Co7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.226Ge0.774\\n\",\n        \"output\": \" No, Si0.226Ge0.774 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrErMg2\\n\",\n        \"output\": \" Yes, PrErMg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmMnO3\\n\",\n        \"output\": \" Yes, TmMnO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr3Li4La5O12\\n\",\n        \"output\": \" Yes, Sr3Li4La5O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrRh\\n\",\n        \"output\": \" Yes, ZrRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2BaNb2Se11\\n\",\n        \"output\": \" No, Rb2BaNb2Se11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In4Te3\\n\",\n        \"output\": \" No, In4Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaC\\n\",\n        \"output\": \" Yes, NaC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2CoWO6\\n\",\n        \"output\": \" Yes, Ba2CoWO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScAg(PSe3)2\\n\",\n        \"output\": \" No, ScAg(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf5Sn3\\n\",\n        \"output\": \" Yes, Hf5Sn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3C\\n\",\n        \"output\": \" Yes, Li3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaYb2O4\\n\",\n        \"output\": \" Yes, BaYb2O4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaIrO3\\n\",\n        \"output\": \" Yes, CaIrO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Er2Fe14B\\n\",\n        \"output\": \" Yes, Er2Fe14B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PW5O17\\n\",\n        \"output\": \" Yes, PW5O17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" size\\n\",\n        \"output\": \" size is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuCu2SnS4\\n\",\n        \"output\": \" No, EuCu2SnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiCdBO3\\n\",\n        \"output\": \" No, LiCdBO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc2GaIr\\n\",\n        \"output\": \" Yes, Sc2GaIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyPO4\\n\",\n        \"output\": \" No, DyPO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca3PbN\\n\",\n        \"output\": \" Yes, Ca3PbN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2GaSn2\\n\",\n        \"output\": \" Yes, V2GaSn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl9SbSe6\\n\",\n        \"output\": \" Yes, Tl9SbSe6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbHg2\\n\",\n        \"output\": \" Yes, TbHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hf2ReRh\\n\",\n        \"output\": \" Yes, Hf2ReRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2SO4\\n\",\n        \"output\": \" Yes, Na2SO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" cold\\n\",\n        \"output\": \" cold is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Sb8Se3\\n\",\n        \"output\": \" No, K2Sb8Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2P2PdSe6\\n\",\n        \"output\": \" No, Cs2P2PdSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1Sb0.35As0.65\\n\",\n        \"output\": \" No, Ga1Sb0.35As0.65 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaSb(PS3)2\\n\",\n        \"output\": \" No, NaSb(PS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Co7Mo6\\n\",\n        \"output\": \" Yes, Co7Mo6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgRh2Pb\\n\",\n        \"output\": \" Yes, MgRh2Pb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TeI\\n\",\n        \"output\": \" No, TeI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SbAs\\n\",\n        \"output\": \" No, SbAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmH2\\n\",\n        \"output\": \" Yes, TmH2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl(Cu3S2)2\\n\",\n        \"output\": \" Yes, Tl(Cu3S2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2GdInSe5\\n\",\n        \"output\": \" No, Ba2GdInSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In2Co\\n\",\n        \"output\": \" Yes, In2Co is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag7(SI)2\\n\",\n        \"output\": \" Yes, Ag7(SI)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu3S4\\n\",\n        \"output\": \" No, Eu3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiBr\\n\",\n        \"output\": \" No, LiBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb(SbTe2)2\\n\",\n        \"output\": \" No, Yb(SbTe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbSmRh2\\n\",\n        \"output\": \" Yes, YbSmRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiMgBi\\n\",\n        \"output\": \" No, LiMgBi is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrIn2\\n\",\n        \"output\": \" Yes, SrIn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbIn4Ni\\n\",\n        \"output\": \" Yes, YbIn4Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" authority\\n\",\n        \"output\": \" authority is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaAlGeS4\\n\",\n        \"output\": \" No, NaAlGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" POsS\\n\",\n        \"output\": \" No, POsS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr6Fe13Si\\n\",\n        \"output\": \" Yes, Pr6Fe13Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" WCl3\\n\",\n        \"output\": \" Yes, WCl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb4Mo5(PO11)2\\n\",\n        \"output\": \" No, Rb4Mo5(PO11)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2AsClO4\\n\",\n        \"output\": \" No, Bi2AsClO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScTlSe2\\n\",\n        \"output\": \" No, ScTlSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CoAsRh\\n\",\n        \"output\": \" Yes, CoAsRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb(Al2Fe)4\\n\",\n        \"output\": \" Yes, Tb(Al2Fe)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb4Sb2S11.25\\n\",\n        \"output\": \" No, Yb4Sb2S11.25 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuScO3\\n\",\n        \"output\": \" Yes, EuScO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U11O5\\n\",\n        \"output\": \" Yes, U11O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2InAgS4\\n\",\n        \"output\": \" No, Ba2InAgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr3(Al2C3)2\\n\",\n        \"output\": \" Yes, Zr3(Al2C3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er5NiPb3\\n\",\n        \"output\": \" Yes, Er5NiPb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" H2Se\\n\",\n        \"output\": \" Yes, H2Se is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaEuO2\\n\",\n        \"output\": \" Yes, NaEuO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbCaBO3\\n\",\n        \"output\": \" No, RbCaBO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BePd2\\n\",\n        \"output\": \" Yes, BePd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2NiIrO6\\n\",\n        \"output\": \" Yes, Ca2NiIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CBr4\\n\",\n        \"output\": \" No, CBr4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnCu2GeSe4\\n\",\n        \"output\": \" No, ZnCu2GeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuB(SbO4)2\\n\",\n        \"output\": \" No, EuB(SbO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" skill\\n\",\n        \"output\": \" skill is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li9Ga13(Te7O22)3\\n\",\n        \"output\": \" No, Li9Ga13(Te7O22)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnO\\n\",\n        \"output\": \" No, MnO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsIn(SnSe3)2\\n\",\n        \"output\": \" No, CsIn(SnSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2NdInSe5\\n\",\n        \"output\": \" No, Ba2NdInSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaTh3\\n\",\n        \"output\": \" Yes, BaTh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaZn5\\n\",\n        \"output\": \" Yes, BaZn5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y(Re2Si)2\\n\",\n        \"output\": \" Yes, Y(Re2Si)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsInTe2\\n\",\n        \"output\": \" No, CsInTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho(SiPt)2\\n\",\n        \"output\": \" Yes, Ho(SiPt)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.75In2.1Ag0.2Te4\\n\",\n        \"output\": \" No, Cd0.75In2.1Ag0.2Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErPbAu\\n\",\n        \"output\": \" Yes, ErPbAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho(SiOs)2\\n\",\n        \"output\": \" Yes, Ho(SiOs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" coal\\n\",\n        \"output\": \" coal is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeO2\\n\",\n        \"output\": \" No, CeO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SiHg3\\n\",\n        \"output\": \" Yes, SiHg3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr(Fe2Si)2\\n\",\n        \"output\": \" Yes, Zr(Fe2Si)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdPbAu\\n\",\n        \"output\": \" Yes, GdPbAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CoH2(SN)4\\n\",\n        \"output\": \" Yes, CoH2(SN)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdNiC2\\n\",\n        \"output\": \" Yes, NdNiC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2Ge5Ir3\\n\",\n        \"output\": \" Yes, La2Ge5Ir3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy2(GePt3)3\\n\",\n        \"output\": \" Yes, Dy2(GePt3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te3As2\\n\",\n        \"output\": \" No, Te3As2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr3Ir\\n\",\n        \"output\": \" Yes, Zr3Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbCl\\n\",\n        \"output\": \" Yes, TbCl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li13Ti22O48\\n\",\n        \"output\": \" Yes, Li13Ti22O48 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsTb9(Cd2Se9)2\\n\",\n        \"output\": \" No, CsTb9(Cd2Se9)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KTa3CuO9\\n\",\n        \"output\": \" Yes, KTa3CuO9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce8U2O21\\n\",\n        \"output\": \" Yes, Ce8U2O21 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaNi5\\n\",\n        \"output\": \" Yes, CaNi5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnAs\\n\",\n        \"output\": \" No, ZnAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K3Nb2AsSe11\\n\",\n        \"output\": \" No, K3Nb2AsSe11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd0.3Hg0.7Se1\\n\",\n        \"output\": \" No, Cd0.3Hg0.7Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdZn\\n\",\n        \"output\": \" Yes, GdZn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta5N6\\n\",\n        \"output\": \" Yes, Ta5N6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuCu9Sn4\\n\",\n        \"output\": \" Yes, EuCu9Sn4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.85Cu0.15Se2.85\\n\",\n        \"output\": \" No, Ga1.85Cu0.15Se2.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GdSb\\n\",\n        \"output\": \" Yes, GdSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga0.99Hg0.01Sb0.99Te0.01\\n\",\n        \"output\": \" No, Ga0.99Hg0.01Sb0.99Te0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GdScS3\\n\",\n        \"output\": \" No, GdScS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrTe\\n\",\n        \"output\": \" No, SrTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.05Cd0.95Sb0.05Te0.95\\n\",\n        \"output\": \" No, Al0.05Cd0.95Sb0.05Te0.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" regret\\n\",\n        \"output\": \" regret is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In5CuS8\\n\",\n        \"output\": \" No, In5CuS8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2UI6\\n\",\n        \"output\": \" Yes, Na2UI6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgSbF6\\n\",\n        \"output\": \" Yes, MgSbF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" wool\\n\",\n        \"output\": \" wool is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2NaMgF6\\n\",\n        \"output\": \" Yes, Cs2NaMgF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2MgSn\\n\",\n        \"output\": \" Yes, Li2MgSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg2Ga\\n\",\n        \"output\": \" Yes, Mg2Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2InBiS5\\n\",\n        \"output\": \" No, Ba2InBiS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.03In0.97Te0.03As0.97\\n\",\n        \"output\": \" No, Cd0.03In0.97Te0.03As0.97 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba(FeS2)2\\n\",\n        \"output\": \" Yes, Ba(FeS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeSiI\\n\",\n        \"output\": \" Yes, CeSiI is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Fe2Cu3O10\\n\",\n        \"output\": \" Yes, Li4Fe2Cu3O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.3Ga0.7P1\\n\",\n        \"output\": \" No, In0.3Ga0.7P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PRuS\\n\",\n        \"output\": \" No, PRuS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Fe10O9F11\\n\",\n        \"output\": \" Yes, Fe10O9F11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce(MnGe)2\\n\",\n        \"output\": \" Yes, Ce(MnGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaAgS2\\n\",\n        \"output\": \" No, GaAgS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaSe\\n\",\n        \"output\": \" No, CaSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.03Te1Pb0.97\\n\",\n        \"output\": \" No, Sn0.03Te1Pb0.97 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nb3V(PO4)6\\n\",\n        \"output\": \" Yes, Nb3V(PO4)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga3Pt2\\n\",\n        \"output\": \" Yes, Ga3Pt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrGe3\\n\",\n        \"output\": \" Yes, PrGe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrGe5\\n\",\n        \"output\": \" Yes, PrGe5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmMg2Sc\\n\",\n        \"output\": \" Yes, TmMg2Sc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi0.2Te0.3Pb0.9Se0.9\\n\",\n        \"output\": \" No, Bi0.2Te0.3Pb0.9Se0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.01Ga0.99P1\\n\",\n        \"output\": \" No, Al0.01Ga0.99P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmHg3\\n\",\n        \"output\": \" Yes, SmHg3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnHgO3\\n\",\n        \"output\": \" No, SnHgO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" UCoSi\\n\",\n        \"output\": \" Yes, UCoSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" InSb2S4Br\\n\",\n        \"output\": \" No, InSb2S4Br is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaSn3\\n\",\n        \"output\": \" Yes, BaSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErBPd3\\n\",\n        \"output\": \" Yes, ErBPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.02Sb0.98Se0.06\\n\",\n        \"output\": \" No, Ga1.02Sb0.98Se0.06 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeCuS2\\n\",\n        \"output\": \" No, FeCuS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YScO2\\n\",\n        \"output\": \" Yes, YScO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnP2\\n\",\n        \"output\": \" Yes, MnP2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiNi2(PO4)3\\n\",\n        \"output\": \" Yes, LiNi2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb3V\\n\",\n        \"output\": \" Yes, Yb3V is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr(PrS2)2\\n\",\n        \"output\": \" No, Sr(PrS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PtS\\n\",\n        \"output\": \" No, PtS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1.95Cu0.05S2.95\\n\",\n        \"output\": \" No, Ga1.95Cu0.05S2.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2NdGaSe5\\n\",\n        \"output\": \" No, Ba2NdGaSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Li3(BO2)5\\n\",\n        \"output\": \" No, Cs2Li3(BO2)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Sn(SbSe4)2\\n\",\n        \"output\": \" No, Ba3Sn(SbSe4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.5Cu0.5S2.5\\n\",\n        \"output\": \" No, Ga1.5Cu0.5S2.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl2PAuS4\\n\",\n        \"output\": \" No, Tl2PAuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdMg2Ni9\\n\",\n        \"output\": \" Yes, NdMg2Ni9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn3(PS4)2\\n\",\n        \"output\": \" No, Zn3(PS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2ZnSn3S8\\n\",\n        \"output\": \" No, K2ZnSn3S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgTe\\n\",\n        \"output\": \" No, AgTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaFe2O3\\n\",\n        \"output\": \" Yes, NaFe2O3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" weather\\n\",\n        \"output\": \" weather is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.5Cd0.5Se1\\n\",\n        \"output\": \" No, Zn0.5Cd0.5Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hf3Zn3N\\n\",\n        \"output\": \" Yes, Hf3Zn3N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" balance\\n\",\n        \"output\": \" balance is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(AsPd)2\\n\",\n        \"output\": \" Yes, Eu(AsPd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TaAlPt\\n\",\n        \"output\": \" Yes, TaAlPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd(CrSi)2\\n\",\n        \"output\": \" Yes, Nd(CrSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba(GaSe2)2\\n\",\n        \"output\": \" No, Ba(GaSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" mile\\n\",\n        \"output\": \" mile is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu3P2\\n\",\n        \"output\": \" No, Eu3P2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy2S3\\n\",\n        \"output\": \" No, Dy2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" IrPb\\n\",\n        \"output\": \" Yes, IrPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg(FeO2)4\\n\",\n        \"output\": \" Yes, Mg(FeO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaNbN2O\\n\",\n        \"output\": \" No, LaNbN2O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na8(CuO2)5\\n\",\n        \"output\": \" Yes, Na8(CuO2)5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnTePd\\n\",\n        \"output\": \" Yes, MnTePd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu10Sb3\\n\",\n        \"output\": \" Yes, Cu10Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GeAs3\\n\",\n        \"output\": \" Yes, GeAs3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3(LiSn2)4\\n\",\n        \"output\": \" Yes, Ba3(LiSn2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FeP4\\n\",\n        \"output\": \" No, FeP4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mo5As4\\n\",\n        \"output\": \" Yes, Mo5As4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge3Bi3O10.5\\n\",\n        \"output\": \" No, Ge3Bi3O10.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdRhF6\\n\",\n        \"output\": \" Yes, CdRhF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.3Ga0.7As0.3P0.7\\n\",\n        \"output\": \" No, In0.3Ga0.7As0.3P0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnCu2Sn\\n\",\n        \"output\": \" Yes, MnCu2Sn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UCo4Sn\\n\",\n        \"output\": \" Yes, UCo4Sn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrTiO3\\n\",\n        \"output\": \" No, SrTiO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaReH9\\n\",\n        \"output\": \" No, BaReH9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiC\\n\",\n        \"output\": \" Yes, TiC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf2Si\\n\",\n        \"output\": \" Yes, Hf2Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hf5CuPb3\\n\",\n        \"output\": \" Yes, Hf5CuPb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrMo3\\n\",\n        \"output\": \" Yes, PrMo3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrMoO4F\\n\",\n        \"output\": \" No, PrMoO4F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb3Al3Ge7Se20\\n\",\n        \"output\": \" No, Rb3Al3Ge7Se20 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaMg3\\n\",\n        \"output\": \" Yes, LaMg3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" B6P\\n\",\n        \"output\": \" No, B6P is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2ZnRh\\n\",\n        \"output\": \" Yes, Ca2ZnRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.8Cu0.2Se2.8\\n\",\n        \"output\": \" No, Ga1.8Cu0.2Se2.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiSe\\n\",\n        \"output\": \" Yes, TiSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hg3As\\n\",\n        \"output\": \" Yes, Hg3As is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TaRh3\\n\",\n        \"output\": \" Yes, TaRh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La3Ge3Br2\\n\",\n        \"output\": \" Yes, La3Ge3Br2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrIr2\\n\",\n        \"output\": \" Yes, PrIr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2.1Bi5.9Pb2S14\\n\",\n        \"output\": \" No, La2.1Bi5.9Pb2S14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.99Ga0.01P0.01Se0.99\\n\",\n        \"output\": \" No, Zn0.99Ga0.01P0.01Se0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc(CuSe)3\\n\",\n        \"output\": \" No, Sc(CuSe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe3Si\\n\",\n        \"output\": \" Yes, Fe3Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CoAs3\\n\",\n        \"output\": \" No, CoAs3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrSiTe\\n\",\n        \"output\": \" Yes, ZrSiTe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cr10Sb3Te7\\n\",\n        \"output\": \" Yes, Cr10Sb3Te7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La(PRu)2\\n\",\n        \"output\": \" Yes, La(PRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" DyB6\\n\",\n        \"output\": \" No, DyB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbZrSb\\n\",\n        \"output\": \" Yes, TbZrSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmBPd3\\n\",\n        \"output\": \" Yes, SmBPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn2SbS2I3\\n\",\n        \"output\": \" No, Sn2SbS2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn3Cr3(CoO8)2\\n\",\n        \"output\": \" Yes, Mn3Cr3(CoO8)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2NdAs2\\n\",\n        \"output\": \" Yes, Li2NdAs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y2O3\\n\",\n        \"output\": \" No, Y2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2EuSn\\n\",\n        \"output\": \" Yes, Li2EuSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc8Te3\\n\",\n        \"output\": \" Yes, Sc8Te3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgO\\n\",\n        \"output\": \" No, MgO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsTm9(Cd2Se9)2\\n\",\n        \"output\": \" No, CsTm9(Cd2Se9)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdP4\\n\",\n        \"output\": \" No, CdP4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(ClO4)3\\n\",\n        \"output\": \" Yes, Eu(ClO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InBi2Se4Br\\n\",\n        \"output\": \" No, InBi2Se4Br is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc6NiTe2\\n\",\n        \"output\": \" Yes, Sc6NiTe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdBi\\n\",\n        \"output\": \" Yes, NdBi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba(InSe2)2\\n\",\n        \"output\": \" No, Ba(InSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y(FeSi)2\\n\",\n        \"output\": \" Yes, Y(FeSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti3Pt5\\n\",\n        \"output\": \" Yes, Ti3Pt5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrNiSn\\n\",\n        \"output\": \" Yes, ZrNiSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbBRh3\\n\",\n        \"output\": \" Yes, TbBRh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsEuF3\\n\",\n        \"output\": \" Yes, CsEuF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Zn(SnS3)2\\n\",\n        \"output\": \" No, Na2Zn(SnS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsBi3Se5\\n\",\n        \"output\": \" No, CsBi3Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.05Sb0.95Se0.15\\n\",\n        \"output\": \" No, Ga1.05Sb0.95Se0.15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgF\\n\",\n        \"output\": \" No, AgF is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" landmine\\n\",\n        \"output\": \" landmine is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2Os2O7\\n\",\n        \"output\": \" Yes, Ca2Os2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" look\\n\",\n        \"output\": \" look is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge(SeO3)2\\n\",\n        \"output\": \" No, Ge(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs1.13Cd1.13Bi2.87Se6\\n\",\n        \"output\": \" No, Cs1.13Cd1.13Bi2.87Se6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LuMnSi\\n\",\n        \"output\": \" Yes, LuMnSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" den\\n\",\n        \"output\": \" den is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Th(FeGe)2\\n\",\n        \"output\": \" Yes, Th(FeGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg4Sc3(SiO3)8\\n\",\n        \"output\": \" Yes, Mg4Sc3(SiO3)8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc4Ge6Rh7\\n\",\n        \"output\": \" Yes, Sc4Ge6Rh7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd1Se0.01S0.99\\n\",\n        \"output\": \" No, Cd1Se0.01S0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BiPbBrO2\\n\",\n        \"output\": \" No, BiPbBrO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GeSe2\\n\",\n        \"output\": \" No, GeSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2HfS5\\n\",\n        \"output\": \" No, La2HfS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2PrIn\\n\",\n        \"output\": \" Yes, Li2PrIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGa2GeSe6\\n\",\n        \"output\": \" No, BaGa2GeSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmTl\\n\",\n        \"output\": \" Yes, TmTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaAgSbS3\\n\",\n        \"output\": \" No, BaAgSbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CoGe\\n\",\n        \"output\": \" Yes, CoGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2ZnO4\\n\",\n        \"output\": \" Yes, V2ZnO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb2Ti3Ge4\\n\",\n        \"output\": \" Yes, Tb2Ti3Ge4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" B3H2Pb2O7.5\\n\",\n        \"output\": \" No, B3H2Pb2O7.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.001Ge0.999\\n\",\n        \"output\": \" No, Si0.001Ge0.999 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm5Ti5O17\\n\",\n        \"output\": \" Yes, Tm5Ti5O17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd3Zr\\n\",\n        \"output\": \" Yes, Nd3Zr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrLa3MnO8\\n\",\n        \"output\": \" Yes, SrLa3MnO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi2SeI2O11\\n\",\n        \"output\": \" No, Bi2SeI2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UP2S9\\n\",\n        \"output\": \" No, UP2S9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3La3(Cu3O7)2\\n\",\n        \"output\": \" No, Ba3La3(Cu3O7)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.43Cd0.57Se1\\n\",\n        \"output\": \" No, Zn0.43Cd0.57Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge(WO3)6\\n\",\n        \"output\": \" Yes, Ge(WO3)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TaCoSn2\\n\",\n        \"output\": \" Yes, TaCoSn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GeS\\n\",\n        \"output\": \" No, GeS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sb2Se3\\n\",\n        \"output\": \" No, Sb2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.005Sb0.995Te0.015\\n\",\n        \"output\": \" No, Ga1.005Sb0.995Te0.015 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr2Au\\n\",\n        \"output\": \" Yes, Pr2Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm4Sb2Se11.68\\n\",\n        \"output\": \" No, Tm4Sb2Se11.68 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.7Ga0.3P0.3S0.7\\n\",\n        \"output\": \" No, Zn0.7Ga0.3P0.3S0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2ZnTe2\\n\",\n        \"output\": \" No, K2ZnTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn6S5Cl2\\n\",\n        \"output\": \" No, Zn6S5Cl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U(SiNi)2\\n\",\n        \"output\": \" Yes, U(SiNi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" P2Se5\\n\",\n        \"output\": \" No, P2Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.2In2.4Ag0.4Te4\\n\",\n        \"output\": \" No, Cd0.2In2.4Ag0.4Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr6NiCl15\\n\",\n        \"output\": \" Yes, Zr6NiCl15 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs10Cd4Sn4S17\\n\",\n        \"output\": \" No, Cs10Cd4Sn4S17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na3Mn2(GeO4)3\\n\",\n        \"output\": \" Yes, Na3Mn2(GeO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs6.4Na1.6Ga8Ge38\\n\",\n        \"output\": \" No, Cs6.4Na1.6Ga8Ge38 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PbSeO4\\n\",\n        \"output\": \" No, PbSeO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr2GeSe5\\n\",\n        \"output\": \" No, Pr2GeSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmIn2Rh\\n\",\n        \"output\": \" Yes, SmIn2Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmB6\\n\",\n        \"output\": \" No, SmB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cr2P3O11\\n\",\n        \"output\": \" Yes, Cr2P3O11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" V3Pt\\n\",\n        \"output\": \" Yes, V3Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsDy9(Cd2Se9)2\\n\",\n        \"output\": \" No, CsDy9(Cd2Se9)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ThSi2Ru3\\n\",\n        \"output\": \" Yes, ThSi2Ru3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FeBi25O39\\n\",\n        \"output\": \" No, FeBi25O39 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y(Al5Fe)2\\n\",\n        \"output\": \" Yes, Y(Al5Fe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Mo2Se2O13\\n\",\n        \"output\": \" No, Bi2Mo2Se2O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaCuTeF\\n\",\n        \"output\": \" No, BaCuTeF is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2VSi\\n\",\n        \"output\": \" Yes, Mn2VSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuHg(SeO3)2\\n\",\n        \"output\": \" No, CuHg(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnCrO2\\n\",\n        \"output\": \" Yes, ZnCrO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf2Al3C4\\n\",\n        \"output\": \" Yes, Hf2Al3C4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HgTe\\n\",\n        \"output\": \" No, HgTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Ni5(PO4)4\\n\",\n        \"output\": \" Yes, Li2Ni5(PO4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm4GaSbS9\\n\",\n        \"output\": \" No, Sm4GaSbS9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsNb6I11\\n\",\n        \"output\": \" Yes, CsNb6I11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuBi3\\n\",\n        \"output\": \" Yes, EuBi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BiSeBr\\n\",\n        \"output\": \" No, BiSeBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.35Ga0.65As1\\n\",\n        \"output\": \" No, Al0.35Ga0.65As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnSb2MoO7\\n\",\n        \"output\": \" No, ZnSb2MoO7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaIn\\n\",\n        \"output\": \" Yes, LaIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaSb\\n\",\n        \"output\": \" No, GaSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaLi3\\n\",\n        \"output\": \" Yes, NaLi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3V12O29\\n\",\n        \"output\": \" Yes, Li3V12O29 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Sb2S7\\n\",\n        \"output\": \" No, Ba3Sb2S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" engineering\\n\",\n        \"output\": \" engineering is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrB6\\n\",\n        \"output\": \" No, PrB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbCd13\\n\",\n        \"output\": \" Yes, RbCd13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiZnBO3\\n\",\n        \"output\": \" No, LiZnBO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaOsO3\\n\",\n        \"output\": \" Yes, CaOsO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.001Sb0.999Se0.003\\n\",\n        \"output\": \" No, Ga1.001Sb0.999Se0.003 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy(CuSe)3\\n\",\n        \"output\": \" No, Dy(CuSe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrIn4Ir\\n\",\n        \"output\": \" Yes, SrIn4Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" As2Os\\n\",\n        \"output\": \" No, As2Os is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y3Fe29\\n\",\n        \"output\": \" Yes, Y3Fe29 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsInS2\\n\",\n        \"output\": \" No, CsInS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeInIr\\n\",\n        \"output\": \" Yes, CeInIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr(Sb3Ru)4\\n\",\n        \"output\": \" Yes, Sr(Sb3Ru)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbCu4AsS4\\n\",\n        \"output\": \" No, RbCu4AsS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnCdO2\\n\",\n        \"output\": \" Yes, MnCdO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" robin\\n\",\n        \"output\": \" robin is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb1.54Cd1.54Bi2.46S6\\n\",\n        \"output\": \" No, Rb1.54Cd1.54Bi2.46S6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiTm2Ru\\n\",\n        \"output\": \" Yes, LiTm2Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Te4MoW3S4\\n\",\n        \"output\": \" Yes, Te4MoW3S4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.05Pb0.95Se1\\n\",\n        \"output\": \" No, Ge0.05Pb0.95Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgTe\\n\",\n        \"output\": \" No, MgTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaAl4Se7\\n\",\n        \"output\": \" No, BaAl4Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy1Te1.45\\n\",\n        \"output\": \" No, Dy1Te1.45 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaIrPb\\n\",\n        \"output\": \" Yes, NaIrPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrNiAs\\n\",\n        \"output\": \" Yes, CrNiAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrInPd2\\n\",\n        \"output\": \" Yes, ZrInPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KAu(IO3)4\\n\",\n        \"output\": \" No, KAu(IO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm2ZnOs\\n\",\n        \"output\": \" Yes, Tm2ZnOs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HgO\\n\",\n        \"output\": \" No, HgO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca(GdS2)2\\n\",\n        \"output\": \" No, Ca(GdS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TeI4\\n\",\n        \"output\": \" No, TeI4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsTiCl3\\n\",\n        \"output\": \" Yes, CsTiCl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaSn3Ru\\n\",\n        \"output\": \" Yes, LaSn3Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu25Se26\\n\",\n        \"output\": \" Yes, Cu25Se26 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm4Al23Ni6\\n\",\n        \"output\": \" Yes, Sm4Al23Ni6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si2Ru\\n\",\n        \"output\": \" Yes, Si2Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KCuSnSe3\\n\",\n        \"output\": \" No, KCuSnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KInGeS4\\n\",\n        \"output\": \" No, KInGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TaAl3\\n\",\n        \"output\": \" Yes, TaAl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaGaS2\\n\",\n        \"output\": \" No, TaGaS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr3Eu(PO4)3\\n\",\n        \"output\": \" No, Sr3Eu(PO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlCoO3\\n\",\n        \"output\": \" Yes, AlCoO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NbSi2\\n\",\n        \"output\": \" Yes, NbSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sb2Te\\n\",\n        \"output\": \" Yes, Sb2Te is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2(SnSe3)3\\n\",\n        \"output\": \" No, Ce2(SnSe3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DySiIr\\n\",\n        \"output\": \" Yes, DySiIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ni(PO3)4\\n\",\n        \"output\": \" Yes, Ni(PO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu7Hg6\\n\",\n        \"output\": \" Yes, Cu7Hg6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PHPbO3\\n\",\n        \"output\": \" No, PHPbO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" lier\\n\",\n        \"output\": \" lier is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbB(SbO4)2\\n\",\n        \"output\": \" No, TbB(SbO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn2InCuTe4\\n\",\n        \"output\": \" No, Zn2InCuTe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmCdHg2\\n\",\n        \"output\": \" Yes, SmCdHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4HgGe2S7\\n\",\n        \"output\": \" No, Li4HgGe2S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V3As2O9\\n\",\n        \"output\": \" No, V3As2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GeAs\\n\",\n        \"output\": \" No, GeAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd2S3\\n\",\n        \"output\": \" No, Gd2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfTiF6\\n\",\n        \"output\": \" Yes, HfTiF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsZn4In5Se12\\n\",\n        \"output\": \" No, CsZn4In5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn3As2\\n\",\n        \"output\": \" No, Sn3As2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbBO3\\n\",\n        \"output\": \" Yes, YbBO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb3CuO8\\n\",\n        \"output\": \" No, Nb3CuO8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdSe\\n\",\n        \"output\": \" No, CdSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta4Cu2O11\\n\",\n        \"output\": \" No, Ta4Cu2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg3AsN\\n\",\n        \"output\": \" No, Mg3AsN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" U2Cl5O2\\n\",\n        \"output\": \" Yes, U2Cl5O2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2ZnSn3Se8\\n\",\n        \"output\": \" No, Cs2ZnSn3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ta7Cu3O19\\n\",\n        \"output\": \" No, Ta7Cu3O19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb3Os\\n\",\n        \"output\": \" Yes, Nb3Os is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4TiCr3O8\\n\",\n        \"output\": \" Yes, Li4TiCr3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Gd(PO4)2\\n\",\n        \"output\": \" No, Na2Gd(PO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb3Bi2I9\\n\",\n        \"output\": \" No, Rb3Bi2I9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiCd2Rh\\n\",\n        \"output\": \" Yes, LiCd2Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.04In0.96Te0.04As0.96\\n\",\n        \"output\": \" No, Cd0.04In0.96Te0.04As0.96 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaLa2TaO6\\n\",\n        \"output\": \" No, NaLa2TaO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbWClO4\\n\",\n        \"output\": \" No, TbWClO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn3NiN\\n\",\n        \"output\": \" Yes, Mn3NiN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlCoMo2\\n\",\n        \"output\": \" Yes, TlCoMo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiF\\n\",\n        \"output\": \" No, LiF is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" P2Se3\\n\",\n        \"output\": \" No, P2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li5Mn2Cu5O12\\n\",\n        \"output\": \" Yes, Li5Mn2Cu5O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U2TeN2\\n\",\n        \"output\": \" Yes, U2TeN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Mn2CuO6\\n\",\n        \"output\": \" Yes, Li3Mn2CuO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuPPt\\n\",\n        \"output\": \" Yes, EuPPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaCuSO\\n\",\n        \"output\": \" No, LaCuSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Mn2(CoO4)2\\n\",\n        \"output\": \" Yes, Li3Mn2(CoO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.98Ge0.02\\n\",\n        \"output\": \" No, Si0.98Ge0.02 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaH3(SeO3)2\\n\",\n        \"output\": \" No, NaH3(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaN\\n\",\n        \"output\": \" No, TaN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba7B3O9F5\\n\",\n        \"output\": \" No, Ba7B3O9F5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaCuSeO\\n\",\n        \"output\": \" No, LaCuSeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga2CuSe4\\n\",\n        \"output\": \" No, Ga2CuSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NiCO4\\n\",\n        \"output\": \" Yes, NiCO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgTi11O20\\n\",\n        \"output\": \" Yes, MgTi11O20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeAl3Ni2\\n\",\n        \"output\": \" Yes, CeAl3Ni2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiSn4Ir\\n\",\n        \"output\": \" Yes, LiSn4Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge3Sb\\n\",\n        \"output\": \" Yes, Ge3Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca3BiAs\\n\",\n        \"output\": \" Yes, Ca3BiAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KInS2\\n\",\n        \"output\": \" No, KInS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AlV(TeO4)2\\n\",\n        \"output\": \" No, AlV(TeO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CrBi2I2O11\\n\",\n        \"output\": \" No, CrBi2I2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd2O3\\n\",\n        \"output\": \" No, Nd2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg3Tl\\n\",\n        \"output\": \" Yes, Mg3Tl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" blade\\n\",\n        \"output\": \" blade is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsAsSe2\\n\",\n        \"output\": \" No, CsAsSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HoCd\\n\",\n        \"output\": \" Yes, HoCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaGaO3\\n\",\n        \"output\": \" No, LaGaO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy2C\\n\",\n        \"output\": \" Yes, Dy2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.99Ga0.01Sb0.01Te0.99\\n\",\n        \"output\": \" No, Zn0.99Ga0.01Sb0.01Te0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K3Ga3Ge7S20\\n\",\n        \"output\": \" No, K3Ga3Ge7S20 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2Se3\\n\",\n        \"output\": \" No, In2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2S3\\n\",\n        \"output\": \" No, Bi2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdAgAs2\\n\",\n        \"output\": \" Yes, NdAgAs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbZn2\\n\",\n        \"output\": \" Yes, TbZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsMn4In5Se12\\n\",\n        \"output\": \" No, CsMn4In5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LuAg2\\n\",\n        \"output\": \" Yes, LuAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.01Pb0.99Se1\\n\",\n        \"output\": \" No, Ge0.01Pb0.99Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaCuO2\\n\",\n        \"output\": \" No, GaCuO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbBa2(PO3)5\\n\",\n        \"output\": \" No, RbBa2(PO3)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaGaGe\\n\",\n        \"output\": \" Yes, CaGaGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al2CoIr\\n\",\n        \"output\": \" Yes, Al2CoIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd(GaSe2)2\\n\",\n        \"output\": \" No, Cd(GaSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgBiPbSe3\\n\",\n        \"output\": \" No, AgBiPbSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnAs\\n\",\n        \"output\": \" Yes, MnAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In4Se3\\n\",\n        \"output\": \" No, In4Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2CdGe\\n\",\n        \"output\": \" No, Li2CdGe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlFeI3\\n\",\n        \"output\": \" Yes, TlFeI3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" cement\\n\",\n        \"output\": \" cement is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UHg3(TeCl3)2\\n\",\n        \"output\": \" No, UHg3(TeCl3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaMg2N2\\n\",\n        \"output\": \" No, CaMg2N2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SiB3\\n\",\n        \"output\": \" No, SiB3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnSe\\n\",\n        \"output\": \" No, ZnSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuZn\\n\",\n        \"output\": \" Yes, EuZn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" FeRhO3\\n\",\n        \"output\": \" Yes, FeRhO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgSbS2\\n\",\n        \"output\": \" No, AgSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbMn4Ga5Te12\\n\",\n        \"output\": \" No, RbMn4Ga5Te12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.7In0.3P1\\n\",\n        \"output\": \" No, Al0.7In0.3P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlS\\n\",\n        \"output\": \" No, TlS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta2Tl4S11\\n\",\n        \"output\": \" No, Ta2Tl4S11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.05Ga0.95Sb0.95Te0.05\\n\",\n        \"output\": \" No, Zn0.05Ga0.95Sb0.95Te0.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AlB12\\n\",\n        \"output\": \" No, AlB12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" wren\\n\",\n        \"output\": \" wren is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd3Ge5\\n\",\n        \"output\": \" Yes, Nd3Ge5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NiGe\\n\",\n        \"output\": \" Yes, NiGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce8Sb2S15\\n\",\n        \"output\": \" No, Ce8Sb2S15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdMg2\\n\",\n        \"output\": \" Yes, NdMg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4Cu(PO4)2\\n\",\n        \"output\": \" Yes, Li4Cu(PO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2O3\\n\",\n        \"output\": \" No, La2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y3Si3Pd2\\n\",\n        \"output\": \" Yes, Y3Si3Pd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Th(Al2Fe)4\\n\",\n        \"output\": \" Yes, Th(Al2Fe)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce6B2(CBr)3\\n\",\n        \"output\": \" Yes, Ce6B2(CBr)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbCdHg2\\n\",\n        \"output\": \" Yes, YbCdHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2SiHgS4\\n\",\n        \"output\": \" No, Li2SiHgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrIn4Pt\\n\",\n        \"output\": \" Yes, SrIn4Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiSnAu\\n\",\n        \"output\": \" Yes, LiSnAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MoSe2\\n\",\n        \"output\": \" No, MoSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnAlAu2\\n\",\n        \"output\": \" Yes, MnAlAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La4Fe(SbS5)2\\n\",\n        \"output\": \" No, La4Fe(SbS5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" fold\\n\",\n        \"output\": \" fold is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2SmGaSe5\\n\",\n        \"output\": \" No, Ba2SmGaSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd3Ni13B2\\n\",\n        \"output\": \" Yes, Nd3Ni13B2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2ErInTe5\\n\",\n        \"output\": \" No, Ba2ErInTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KSb\\n\",\n        \"output\": \" No, KSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KPPbO4\\n\",\n        \"output\": \" No, KPPbO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg2Co\\n\",\n        \"output\": \" No, Mg2Co is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlBr\\n\",\n        \"output\": \" No, TlBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3Au\\n\",\n        \"output\": \" Yes, Ca3Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BPb6BrO7\\n\",\n        \"output\": \" No, BPb6BrO7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PdPb2\\n\",\n        \"output\": \" Yes, PdPb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrAs\\n\",\n        \"output\": \" Yes, CrAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" P2H4RhO9\\n\",\n        \"output\": \" Yes, P2H4RhO9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiZrRh2\\n\",\n        \"output\": \" Yes, LiZrRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaMnO3\\n\",\n        \"output\": \" Yes, BaMnO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnF2\\n\",\n        \"output\": \" No, MnF2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrAs\\n\",\n        \"output\": \" No, PrAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.2In0.8P1\\n\",\n        \"output\": \" No, Al0.2In0.8P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La1Se0.14S1.86\\n\",\n        \"output\": \" No, La1Se0.14S1.86 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb3(Fe10B3)2\\n\",\n        \"output\": \" Yes, Nb3(Fe10B3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba5In4Bi5\\n\",\n        \"output\": \" Yes, Ba5In4Bi5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2ScSbO6\\n\",\n        \"output\": \" No, Sr2ScSbO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(GeRh)2\\n\",\n        \"output\": \" Yes, Ca(GeRh)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi2(BO3)3\\n\",\n        \"output\": \" Yes, Bi2(BO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li5Mn5(SbO6)2\\n\",\n        \"output\": \" Yes, Li5Mn5(SbO6)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" FeCo2Si\\n\",\n        \"output\": \" Yes, FeCo2Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AlSn\\n\",\n        \"output\": \" Yes, AlSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmAu\\n\",\n        \"output\": \" Yes, TmAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti4O5\\n\",\n        \"output\": \" Yes, Ti4O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2Ga8SiS16\\n\",\n        \"output\": \" No, Ba2Ga8SiS16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyAgHg2\\n\",\n        \"output\": \" Yes, DyAgHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Cd1.35Hg4.65S7\\n\",\n        \"output\": \" No, Cs2Cd1.35Hg4.65S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho3P\\n\",\n        \"output\": \" Yes, Ho3P is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb2SbO2\\n\",\n        \"output\": \" Yes, Tb2SbO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrN2\\n\",\n        \"output\": \" Yes, SrN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbNb4Br11\\n\",\n        \"output\": \" No, RbNb4Br11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdTe\\n\",\n        \"output\": \" Yes, NdTe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdB6\\n\",\n        \"output\": \" No, NdB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Ga2SnS6\\n\",\n        \"output\": \" No, Na2Ga2SnS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmS\\n\",\n        \"output\": \" No, SmS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te2Pd3Pb2\\n\",\n        \"output\": \" Yes, Te2Pd3Pb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HgCl2\\n\",\n        \"output\": \" No, HgCl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge3Ru2\\n\",\n        \"output\": \" No, Ge3Ru2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2Cu2Sb2S5\\n\",\n        \"output\": \" No, Rb2Cu2Sb2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In3CuS5\\n\",\n        \"output\": \" No, In3CuS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba5Bi3\\n\",\n        \"output\": \" Yes, Ba5Bi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K3Cd(BO2)5\\n\",\n        \"output\": \" No, K3Cd(BO2)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr0.67Ta1.33N3.03O0.12\\n\",\n        \"output\": \" No, Zr0.67Ta1.33N3.03O0.12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnSnP2\\n\",\n        \"output\": \" No, ZnSnP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi1.6Sb0.4Te3\\n\",\n        \"output\": \" No, Bi1.6Sb0.4Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaBeB3O7\\n\",\n        \"output\": \" No, LaBeB3O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlBiTe3\\n\",\n        \"output\": \" No, TlBiTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb(CoGe)2\\n\",\n        \"output\": \" Yes, Tb(CoGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba8Al10B12O41\\n\",\n        \"output\": \" No, Ba8Al10B12O41 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" deborah\\n\",\n        \"output\": \" deborah is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3Tb2(PS4)4\\n\",\n        \"output\": \" No, Ba3Tb2(PS4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuSbSe2\\n\",\n        \"output\": \" No, CuSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.15Te0.15Pb0.85Se0.85\\n\",\n        \"output\": \" No, Ge0.15Te0.15Pb0.85Se0.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca(SiPd)2\\n\",\n        \"output\": \" Yes, Ca(SiPd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Gd2Sb2Se9\\n\",\n        \"output\": \" No, K2Gd2Sb2Se9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2SeClF6\\n\",\n        \"output\": \" Yes, Cs2SeClF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl3VS4\\n\",\n        \"output\": \" No, Tl3VS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.01Sb0.99Se0.03\\n\",\n        \"output\": \" No, Ga1.01Sb0.99Se0.03 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Cd0.25Hg5.75S7\\n\",\n        \"output\": \" No, Cs2Cd0.25Hg5.75S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te2Mo2WSe4\\n\",\n        \"output\": \" Yes, Te2Mo2WSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2BaNb2S11\\n\",\n        \"output\": \" No, K2BaNb2S11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sb5IO7\\n\",\n        \"output\": \" No, Sb5IO7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li8PO3\\n\",\n        \"output\": \" Yes, Li8PO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm3Zr\\n\",\n        \"output\": \" Yes, Sm3Zr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2In2GeS6\\n\",\n        \"output\": \" No, Na2In2GeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdAl7Au3\\n\",\n        \"output\": \" Yes, NdAl7Au3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta2TlO6\\n\",\n        \"output\": \" Yes, Ta2TlO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.162Ge0.838\\n\",\n        \"output\": \" No, Si0.162Ge0.838 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YAgO3\\n\",\n        \"output\": \" Yes, YAgO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1Sb0.1As0.9\\n\",\n        \"output\": \" No, In1Sb0.1As0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi3I4O13F3\\n\",\n        \"output\": \" No, Bi3I4O13F3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsGdO3\\n\",\n        \"output\": \" Yes, CsGdO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Co5SbO12\\n\",\n        \"output\": \" Yes, Li4Co5SbO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ni3Pt\\n\",\n        \"output\": \" Yes, Ni3Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaTb3\\n\",\n        \"output\": \" Yes, LaTb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrSnO3\\n\",\n        \"output\": \" No, SrSnO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In2HgTe4\\n\",\n        \"output\": \" No, In2HgTe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdCu2SnSe4\\n\",\n        \"output\": \" No, CdCu2SnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2Sb7HO14\\n\",\n        \"output\": \" No, Ba2Sb7HO14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HgRhO3\\n\",\n        \"output\": \" Yes, HgRhO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm3Al\\n\",\n        \"output\": \" Yes, Sm3Al is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KScO3\\n\",\n        \"output\": \" Yes, KScO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PmGaAu2\\n\",\n        \"output\": \" Yes, PmGaAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs4Ge(PSe3)4\\n\",\n        \"output\": \" No, Cs4Ge(PSe3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" freon\\n\",\n        \"output\": \" freon is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NiGePt2\\n\",\n        \"output\": \" Yes, NiGePt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiGeRh2\\n\",\n        \"output\": \" Yes, LiGeRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Be2W\\n\",\n        \"output\": \" Yes, Be2W is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si2Te3\\n\",\n        \"output\": \" No, Si2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca3Al2Ge3\\n\",\n        \"output\": \" Yes, Ca3Al2Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4Sb3S8Cl\\n\",\n        \"output\": \" No, Ba4Sb3S8Cl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdTlPd\\n\",\n        \"output\": \" Yes, NdTlPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnSb3(PO4)4\\n\",\n        \"output\": \" Yes, SnSb3(PO4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbSb4Te7\\n\",\n        \"output\": \" No, YbSb4Te7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.8Hg0.2Se1\\n\",\n        \"output\": \" No, Zn0.8Hg0.2Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" meal\\n\",\n        \"output\": \" meal is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YZnBiO4\\n\",\n        \"output\": \" No, YZnBiO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu2CdAg\\n\",\n        \"output\": \" Yes, Lu2CdAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbPbIO2\\n\",\n        \"output\": \" No, SbPbIO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y2CuO4\\n\",\n        \"output\": \" Yes, Y2CuO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" pisces\\n\",\n        \"output\": \" pisces is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu(InS2)3\\n\",\n        \"output\": \" No, Lu(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2FeGeS4\\n\",\n        \"output\": \" No, Li2FeGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li8IrO6\\n\",\n        \"output\": \" Yes, Li8IrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Ge3(BO5)2\\n\",\n        \"output\": \" No, K2Ge3(BO5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScAlNi2\\n\",\n        \"output\": \" Yes, ScAlNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te2Pd\\n\",\n        \"output\": \" No, Te2Pd is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba8Sn4S15\\n\",\n        \"output\": \" No, Ba8Sn4S15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgBi(PSe3)2\\n\",\n        \"output\": \" No, AgBi(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KTbSe4\\n\",\n        \"output\": \" No, KTbSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2ZnGeSe4\\n\",\n        \"output\": \" No, Li2ZnGeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2B6H4O13\\n\",\n        \"output\": \" No, Ba2B6H4O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce3Pd5\\n\",\n        \"output\": \" Yes, Ce3Pd5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrS\\n\",\n        \"output\": \" No, SrS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2Ga0.33Sb1S5\\n\",\n        \"output\": \" No, La2Ga0.33Sb1S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho2O3\\n\",\n        \"output\": \" No, Ho2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiBePt2\\n\",\n        \"output\": \" Yes, LiBePt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb3Bi\\n\",\n        \"output\": \" Yes, Nb3Bi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al(NiS2)2\\n\",\n        \"output\": \" Yes, Al(NiS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCdInSe3\\n\",\n        \"output\": \" No, CsCdInSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfPt\\n\",\n        \"output\": \" Yes, HfPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" P2Pd\\n\",\n        \"output\": \" No, P2Pd is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsInGeSe4\\n\",\n        \"output\": \" No, CsInGeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Ti5Cr3O16\\n\",\n        \"output\": \" Yes, Li4Ti5Cr3O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KYbSe2\\n\",\n        \"output\": \" Yes, KYbSe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb(MnAs)2\\n\",\n        \"output\": \" Yes, Yb(MnAs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Hg3Se2.97S1.03\\n\",\n        \"output\": \" No, K2Hg3Se2.97S1.03 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" brain\\n\",\n        \"output\": \" brain is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy(CuSi)2\\n\",\n        \"output\": \" Yes, Dy(CuSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1.5Cu0.5Se2.5\\n\",\n        \"output\": \" No, Ga1.5Cu0.5Se2.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.9Ga0.1As0.1Se0.9\\n\",\n        \"output\": \" No, Zn0.9Ga0.1As0.1Se0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In5AgS8\\n\",\n        \"output\": \" No, In5AgS8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce5CuSe8\\n\",\n        \"output\": \" Yes, Ce5CuSe8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YMgAl\\n\",\n        \"output\": \" Yes, YMgAl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr3Ge(SbSe4)2\\n\",\n        \"output\": \" No, Sr3Ge(SbSe4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VNi2\\n\",\n        \"output\": \" Yes, VNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoB4\\n\",\n        \"output\": \" Yes, HoB4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc6Te2Os\\n\",\n        \"output\": \" Yes, Sc6Te2Os is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgRhF6\\n\",\n        \"output\": \" Yes, MgRhF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCeHgSe3\\n\",\n        \"output\": \" No, CsCeHgSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaGa\\n\",\n        \"output\": \" Yes, LaGa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AsS3\\n\",\n        \"output\": \" No, AsS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.6Ge0.4\\n\",\n        \"output\": \" No, Si0.6Ge0.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YB2Rh2C\\n\",\n        \"output\": \" Yes, YB2Rh2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrGaAu2\\n\",\n        \"output\": \" Yes, PrGaAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiZn3\\n\",\n        \"output\": \" Yes, TiZn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmAu3\\n\",\n        \"output\": \" Yes, SmAu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiSm3SiS7\\n\",\n        \"output\": \" No, LiSm3SiS7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbAgGe\\n\",\n        \"output\": \" Yes, YbAgGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnAs2\\n\",\n        \"output\": \" No, ZnAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2CrF6\\n\",\n        \"output\": \" Yes, Rb2CrF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K3Ta2AsSe11\\n\",\n        \"output\": \" No, K3Ta2AsSe11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg2CrN2\\n\",\n        \"output\": \" Yes, Mg2CrN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.05Ga0.95Sb0.95Te0.05\\n\",\n        \"output\": \" No, Cd0.05Ga0.95Sb0.95Te0.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti3PO7\\n\",\n        \"output\": \" Yes, Ti3PO7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb11S16\\n\",\n        \"output\": \" Yes, Tb11S16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.8Ga0.2P1\\n\",\n        \"output\": \" No, Al0.8Ga0.2P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr3(Al2Si3)2\\n\",\n        \"output\": \" Yes, Pr3(Al2Si3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2FeWO6\\n\",\n        \"output\": \" Yes, Li2FeWO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr3Se4\\n\",\n        \"output\": \" No, Cr3Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErN\\n\",\n        \"output\": \" No, ErN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sb2Os\\n\",\n        \"output\": \" No, Sb2Os is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Lu2CrS4\\n\",\n        \"output\": \" No, Lu2CrS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.6In0.4P1\\n\",\n        \"output\": \" No, Al0.6In0.4P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc2Fe\\n\",\n        \"output\": \" No, Sc2Fe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsVP2S7\\n\",\n        \"output\": \" Yes, CsVP2S7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeBC\\n\",\n        \"output\": \" Yes, CeBC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" dress\\n\",\n        \"output\": \" dress is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf5Te4\\n\",\n        \"output\": \" Yes, Hf5Te4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AsBr3\\n\",\n        \"output\": \" No, AsBr3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2Zn0.2B2S5.2\\n\",\n        \"output\": \" No, Ba2Zn0.2B2S5.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Te2.4Se0.6\\n\",\n        \"output\": \" No, Bi2Te2.4Se0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd4Ge3Rh4\\n\",\n        \"output\": \" Yes, Nd4Ge3Rh4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K3Ti2P5S18\\n\",\n        \"output\": \" No, K3Ti2P5S18 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.2Ga0.8As0.2P0.8\\n\",\n        \"output\": \" No, In0.2Ga0.8As0.2P0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.3Ga0.7As1\\n\",\n        \"output\": \" No, Al0.3Ga0.7As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaAgTe2\\n\",\n        \"output\": \" No, GaAgTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdAg\\n\",\n        \"output\": \" Yes, CdAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" behavior\\n\",\n        \"output\": \" behavior is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaAlCu4O7\\n\",\n        \"output\": \" Yes, BaAlCu4O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Bi\\n\",\n        \"output\": \" No, Li3Bi is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs(AsRu)2\\n\",\n        \"output\": \" Yes, Cs(AsRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2MnGeS4\\n\",\n        \"output\": \" No, Li2MnGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCu2SbS3\\n\",\n        \"output\": \" No, CsCu2SbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd4As2Br3\\n\",\n        \"output\": \" No, Cd4As2Br3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScHg\\n\",\n        \"output\": \" No, ScHg is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Th(SiRu)2\\n\",\n        \"output\": \" Yes, Th(SiRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" check\\n\",\n        \"output\": \" check is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2OsRu\\n\",\n        \"output\": \" Yes, V2OsRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2GeB4O9\\n\",\n        \"output\": \" No, Rb2GeB4O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Co2(GeO4)3\\n\",\n        \"output\": \" Yes, Li3Co2(GeO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuO\\n\",\n        \"output\": \" No, EuO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li9Fe3(WO4)7\\n\",\n        \"output\": \" Yes, Li9Fe3(WO4)7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2Fe3SnO8\\n\",\n        \"output\": \" Yes, Li2Fe3SnO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K3B6ClO10\\n\",\n        \"output\": \" No, K3B6ClO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na8NbO6\\n\",\n        \"output\": \" Yes, Na8NbO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaBi\\n\",\n        \"output\": \" No, GaBi is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu2ReO5\\n\",\n        \"output\": \" Yes, Eu2ReO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiSe\\n\",\n        \"output\": \" No, BiSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ni23B6\\n\",\n        \"output\": \" Yes, Ni23B6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaSbS2\\n\",\n        \"output\": \" No, NaSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YB2C\\n\",\n        \"output\": \" Yes, YB2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti1C0.9\\n\",\n        \"output\": \" No, Ti1C0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KCoO2\\n\",\n        \"output\": \" Yes, KCoO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba7(SnS3)5\\n\",\n        \"output\": \" No, Ba7(SnS3)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Si3Ag2\\n\",\n        \"output\": \" Yes, Li3Si3Ag2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InAu3\\n\",\n        \"output\": \" Yes, InAu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu2H3ClO3\\n\",\n        \"output\": \" Yes, Cu2H3ClO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na9(WO3)16\\n\",\n        \"output\": \" Yes, Na9(WO3)16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmAlCu\\n\",\n        \"output\": \" Yes, TmAlCu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y2Ge5Ir3\\n\",\n        \"output\": \" Yes, Y2Ge5Ir3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiGaAg2\\n\",\n        \"output\": \" Yes, LiGaAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba6Ga2SnSe11\\n\",\n        \"output\": \" No, Ba6Ga2SnSe11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2In4Se6S\\n\",\n        \"output\": \" No, Na2In4Se6S is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb5Tl3\\n\",\n        \"output\": \" Yes, Tb5Tl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd2Te3\\n\",\n        \"output\": \" No, Gd2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaCuTe2\\n\",\n        \"output\": \" No, GaCuTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiZnN\\n\",\n        \"output\": \" No, LiZnN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li6(NiO2)5\\n\",\n        \"output\": \" Yes, Li6(NiO2)5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiAsS2\\n\",\n        \"output\": \" No, LiAsS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiTm2Rh\\n\",\n        \"output\": \" Yes, LiTm2Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In6S7\\n\",\n        \"output\": \" No, In6S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KSc(SeO3)2\\n\",\n        \"output\": \" No, KSc(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2HgSe4\\n\",\n        \"output\": \" No, Ga2HgSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaCd2Au\\n\",\n        \"output\": \" Yes, NaCd2Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.42Ga0.58As0.58Se0.42\\n\",\n        \"output\": \" No, Zn0.42Ga0.58As0.58Se0.42 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfS2\\n\",\n        \"output\": \" No, HfS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Fe4O7F\\n\",\n        \"output\": \" Yes, Fe4O7F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScRh\\n\",\n        \"output\": \" Yes, ScRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li8BiS6\\n\",\n        \"output\": \" Yes, Li8BiS6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoMgAu2\\n\",\n        \"output\": \" Yes, HoMgAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La4InSbSe9\\n\",\n        \"output\": \" No, La4InSbSe9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga3CuSe5\\n\",\n        \"output\": \" No, Ga3CuSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Ti(AgS2)2\\n\",\n        \"output\": \" No, Cs2Ti(AgS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu2TlAg\\n\",\n        \"output\": \" Yes, Lu2TlAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rh0.67Se2\\n\",\n        \"output\": \" No, Rh0.67Se2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KSbS2\\n\",\n        \"output\": \" No, KSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiAgF3\\n\",\n        \"output\": \" Yes, LiAgF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.95Ga0.05P0.05S0.95\\n\",\n        \"output\": \" No, Zn0.95Ga0.05P0.05S0.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.6Hg0.4Se1\\n\",\n        \"output\": \" No, Cd0.6Hg0.4Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu3SbS4\\n\",\n        \"output\": \" No, Cu3SbS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti4ZnO8\\n\",\n        \"output\": \" Yes, Ti4ZnO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmAs2Au\\n\",\n        \"output\": \" Yes, SmAs2Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl2Hg3Te4\\n\",\n        \"output\": \" No, Tl2Hg3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" POsSe\\n\",\n        \"output\": \" No, POsSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cr4As3\\n\",\n        \"output\": \" Yes, Cr4As3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlSe\\n\",\n        \"output\": \" No, TlSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SiSb3\\n\",\n        \"output\": \" Yes, SiSb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BeFe2Si\\n\",\n        \"output\": \" Yes, BeFe2Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hg5AsS2I3\\n\",\n        \"output\": \" No, Hg5AsS2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsCd4Ga5S12\\n\",\n        \"output\": \" No, CsCd4Ga5S12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na8Hg3\\n\",\n        \"output\": \" Yes, Na8Hg3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnGeN2\\n\",\n        \"output\": \" No, ZnGeN2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" B4C\\n\",\n        \"output\": \" No, B4C is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd0.06In0.94Te0.06As0.94\\n\",\n        \"output\": \" No, Cd0.06In0.94Te0.06As0.94 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2ScTaO6\\n\",\n        \"output\": \" No, Ba2ScTaO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdBiClO2\\n\",\n        \"output\": \" No, CdBiClO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" flesh\\n\",\n        \"output\": \" flesh is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al9Ir2\\n\",\n        \"output\": \" Yes, Al9Ir2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlAsS2\\n\",\n        \"output\": \" No, TlAsS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InSn2As2Se\\n\",\n        \"output\": \" No, InSn2As2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2PC\\n\",\n        \"output\": \" Yes, La2PC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.65Cu0.35Se2.65\\n\",\n        \"output\": \" No, Ga1.65Cu0.35Se2.65 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La4Fe(SbSe5)2\\n\",\n        \"output\": \" No, La4Fe(SbSe5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba(AsPd)2\\n\",\n        \"output\": \" Yes, Ba(AsPd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiGaO2\\n\",\n        \"output\": \" No, LiGaO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdB66\\n\",\n        \"output\": \" No, GdB66 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2LiTa\\n\",\n        \"output\": \" Yes, Na2LiTa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho(CuO2)2\\n\",\n        \"output\": \" Yes, Ho(CuO2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.8In2.1Ag0.1Te4\\n\",\n        \"output\": \" No, Cd0.8In2.1Ag0.1Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlInS2\\n\",\n        \"output\": \" No, TlInS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag3AsS3\\n\",\n        \"output\": \" No, Ag3AsS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgAsSe2\\n\",\n        \"output\": \" No, AgAsSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga0.9Hg0.1Sb0.9Te0.1\\n\",\n        \"output\": \" No, Ga0.9Hg0.1Sb0.9Te0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaSbF6\\n\",\n        \"output\": \" No, NaSbF6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu3TlC\\n\",\n        \"output\": \" Yes, Lu3TlC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr8Al7\\n\",\n        \"output\": \" Yes, Sr8Al7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm3B(SO)3\\n\",\n        \"output\": \" No, Sm3B(SO)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2Mn(SeO)2\\n\",\n        \"output\": \" No, La2Mn(SeO)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsGeI3\\n\",\n        \"output\": \" No, CsGeI3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CrTe2\\n\",\n        \"output\": \" No, CrTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbAg2\\n\",\n        \"output\": \" Yes, YbAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ThS\\n\",\n        \"output\": \" Yes, ThS is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmCoC2\\n\",\n        \"output\": \" Yes, SmCoC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu7(NiTe)2\\n\",\n        \"output\": \" Yes, Lu7(NiTe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.7Ga0.3P0.3Se0.7\\n\",\n        \"output\": \" No, Zn0.7Ga0.3P0.3Se0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PmCd3\\n\",\n        \"output\": \" Yes, PmCd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmSb2\\n\",\n        \"output\": \" Yes, SmSb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaNb2PS10\\n\",\n        \"output\": \" No, NaNb2PS10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2DyInTe5\\n\",\n        \"output\": \" No, Ba2DyInTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuSbPbS3\\n\",\n        \"output\": \" No, CuSbPbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag2PdO2\\n\",\n        \"output\": \" No, Ag2PdO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl3Si\\n\",\n        \"output\": \" Yes, Tl3Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb2O3\\n\",\n        \"output\": \" No, Tb2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb2Te3\\n\",\n        \"output\": \" No, Sb2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiLu2Ga\\n\",\n        \"output\": \" Yes, LiLu2Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KBi2\\n\",\n        \"output\": \" Yes, KBi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2Tl2O7\\n\",\n        \"output\": \" Yes, Mn2Tl2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si2NiP3\\n\",\n        \"output\": \" Yes, Si2NiP3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb2Ge2Ir\\n\",\n        \"output\": \" Yes, Yb2Ge2Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.08Pb0.92Se1\\n\",\n        \"output\": \" No, Sn0.08Pb0.92Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2Tl\\n\",\n        \"output\": \" Yes, Sm2Tl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiCa2In\\n\",\n        \"output\": \" Yes, LiCa2In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrO\\n\",\n        \"output\": \" No, SrO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na4Al4Si19\\n\",\n        \"output\": \" No, Na4Al4Si19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrLi4(BO3)2\\n\",\n        \"output\": \" No, SrLi4(BO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InBi2S4Br\\n\",\n        \"output\": \" No, InBi2S4Br is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2YInSe5\\n\",\n        \"output\": \" No, Ba2YInSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaPd3S4\\n\",\n        \"output\": \" Yes, LaPd3S4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er(CuGe)2\\n\",\n        \"output\": \" Yes, Er(CuGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" liquid\\n\",\n        \"output\": \" liquid is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al2Ru\\n\",\n        \"output\": \" Yes, Al2Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScBe5\\n\",\n        \"output\": \" Yes, ScBe5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg5Ti13O30\\n\",\n        \"output\": \" Yes, Mg5Ti13O30 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.15Te1Pb0.85\\n\",\n        \"output\": \" No, Sn0.15Te1Pb0.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2PdSe8\\n\",\n        \"output\": \" No, Cs2PdSe8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KCd4Ga5Se12\\n\",\n        \"output\": \" No, KCd4Ga5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiInSn\\n\",\n        \"output\": \" Yes, LiInSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UHg4(AsCl3)2\\n\",\n        \"output\": \" No, UHg4(AsCl3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na3Sn2ClF6\\n\",\n        \"output\": \" No, Na3Sn2ClF6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2UCuO6\\n\",\n        \"output\": \" Yes, Ba2UCuO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pd3(PbS)2\\n\",\n        \"output\": \" Yes, Pd3(PbS)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd4O3F7\\n\",\n        \"output\": \" Yes, Nd4O3F7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" tractor\\n\",\n        \"output\": \" tractor is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2NbCuSe4\\n\",\n        \"output\": \" No, Rb2NbCuSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" cry\\n\",\n        \"output\": \" cry is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb11(Ni10C)6\\n\",\n        \"output\": \" Yes, Yb11(Ni10C)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UFeSi\\n\",\n        \"output\": \" Yes, UFeSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg2Ge\\n\",\n        \"output\": \" No, Mg2Ge is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca5Au2\\n\",\n        \"output\": \" Yes, Ca5Au2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeCd2Ag\\n\",\n        \"output\": \" Yes, CeCd2Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuScRh2\\n\",\n        \"output\": \" Yes, LuScRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ni4(BiO2)9\\n\",\n        \"output\": \" Yes, Ni4(BiO2)9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ni2Mo3N\\n\",\n        \"output\": \" Yes, Ni2Mo3N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaBiAu2\\n\",\n        \"output\": \" Yes, LaBiAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K4Nb2S11\\n\",\n        \"output\": \" No, K4Nb2S11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y(SiPt)2\\n\",\n        \"output\": \" Yes, Y(SiPt)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsTa3(SeO6)2\\n\",\n        \"output\": \" No, CsTa3(SeO6)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiHg2Pd\\n\",\n        \"output\": \" Yes, LiHg2Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl2Hg3S4\\n\",\n        \"output\": \" No, Tl2Hg3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er(CrSi)2\\n\",\n        \"output\": \" Yes, Er(CrSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho(CuTe)3\\n\",\n        \"output\": \" No, Ho(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn5O3F5\\n\",\n        \"output\": \" Yes, Mn5O3F5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2HgGe\\n\",\n        \"output\": \" No, Li2HgGe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsWCl6\\n\",\n        \"output\": \" Yes, CsWCl6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrO3\\n\",\n        \"output\": \" No, CrO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FeBi(SeO3)3\\n\",\n        \"output\": \" No, FeBi(SeO3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsZn2B3O7\\n\",\n        \"output\": \" No, CsZn2B3O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" As2S5\\n\",\n        \"output\": \" No, As2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K(CoSe)2\\n\",\n        \"output\": \" Yes, K(CoSe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb5Li6(BO2)11\\n\",\n        \"output\": \" No, Rb5Li6(BO2)11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmHgPd\\n\",\n        \"output\": \" Yes, SmHgPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KSiBiS4\\n\",\n        \"output\": \" No, KSiBiS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrPb3\\n\",\n        \"output\": \" Yes, SrPb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YNiSb\\n\",\n        \"output\": \" No, YNiSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbEuO2\\n\",\n        \"output\": \" Yes, RbEuO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KCuPO4\\n\",\n        \"output\": \" Yes, KCuPO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SiP\\n\",\n        \"output\": \" No, SiP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nb2Cr4Si5\\n\",\n        \"output\": \" Yes, Nb2Cr4Si5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HgIrO3\\n\",\n        \"output\": \" Yes, HgIrO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd4InSbSe9\\n\",\n        \"output\": \" No, Nd4InSbSe9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2GdInTe5\\n\",\n        \"output\": \" No, Ba2GdInTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na7(CoO3)2\\n\",\n        \"output\": \" No, Na7(CoO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KPAu5S8\\n\",\n        \"output\": \" No, KPAu5S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti5Zn4(TeO6)3\\n\",\n        \"output\": \" Yes, Ti5Zn4(TeO6)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Si0.999Ge0.001\\n\",\n        \"output\": \" No, Si0.999Ge0.001 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Zn3(SeO3)4\\n\",\n        \"output\": \" No, Na2Zn3(SeO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmCuSO\\n\",\n        \"output\": \" No, SmCuSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" VPO4\\n\",\n        \"output\": \" Yes, VPO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VTeHO5\\n\",\n        \"output\": \" No, VTeHO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaIn2Ir\\n\",\n        \"output\": \" Yes, CaIn2Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrO\\n\",\n        \"output\": \" No, PrO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HgI\\n\",\n        \"output\": \" No, HgI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaYbInSe4\\n\",\n        \"output\": \" Yes, CaYbInSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmTmZn2\\n\",\n        \"output\": \" Yes, SmTmZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErLu3\\n\",\n        \"output\": \" Yes, ErLu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2V2Te2O11\\n\",\n        \"output\": \" No, Ba2V2Te2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Ho4Cu4S9\\n\",\n        \"output\": \" No, K2Ho4Cu4S9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrZn\\n\",\n        \"output\": \" Yes, PrZn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K3Sn\\n\",\n        \"output\": \" Yes, K3Sn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2Co9O13\\n\",\n        \"output\": \" Yes, Ca2Co9O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na3Sb\\n\",\n        \"output\": \" No, Na3Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La3Si1Sb0.33Se7\\n\",\n        \"output\": \" No, La3Si1Sb0.33Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaTc2W\\n\",\n        \"output\": \" Yes, GaTc2W is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" thomas\\n\",\n        \"output\": \" thomas is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.4Ga0.6P1\\n\",\n        \"output\": \" No, Al0.4Ga0.6P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiPO4\\n\",\n        \"output\": \" Yes, TiPO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Mn2(PO4)3\\n\",\n        \"output\": \" Yes, Li3Mn2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiPbClO2\\n\",\n        \"output\": \" No, BiPbClO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyBiPd\\n\",\n        \"output\": \" Yes, DyBiPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdGeP2\\n\",\n        \"output\": \" No, CdGeP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb(Ni2P)2\\n\",\n        \"output\": \" Yes, Tb(Ni2P)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiTi11O20\\n\",\n        \"output\": \" Yes, LiTi11O20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgAu3\\n\",\n        \"output\": \" Yes, AgAu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoB2Rh3\\n\",\n        \"output\": \" Yes, HoB2Rh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Th2Se5\\n\",\n        \"output\": \" No, Th2Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Re2PbO6\\n\",\n        \"output\": \" Yes, Re2PbO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(BIr)2\\n\",\n        \"output\": \" Yes, Ca(BIr)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1Sb0.6As0.4\\n\",\n        \"output\": \" No, In1Sb0.6As0.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sb2PbSe4\\n\",\n        \"output\": \" No, Sb2PbSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YCo2\\n\",\n        \"output\": \" Yes, YCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.25Ga0.75P0.75Se0.25\\n\",\n        \"output\": \" No, Zn0.25Ga0.75P0.75Se0.25 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd1.47Mn2.04In0.49S5\\n\",\n        \"output\": \" No, Gd1.47Mn2.04In0.49S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2Fe17\\n\",\n        \"output\": \" Yes, Sm2Fe17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu9S5\\n\",\n        \"output\": \" Yes, Cu9S5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrZnSb2\\n\",\n        \"output\": \" Yes, SrZnSb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.99Hg0.01Se1\\n\",\n        \"output\": \" No, Zn0.99Hg0.01Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Mn(WO4)3\\n\",\n        \"output\": \" Yes, Li4Mn(WO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2Cu5F14\\n\",\n        \"output\": \" Yes, Ba2Cu5F14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoSi\\n\",\n        \"output\": \" Yes, HoSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag2BiO3\\n\",\n        \"output\": \" Yes, Ag2BiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsLiCO3\\n\",\n        \"output\": \" No, CsLiCO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu(NO3)2\\n\",\n        \"output\": \" Yes, Cu(NO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnTe9\\n\",\n        \"output\": \" No, MnTe9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm2Ga10Os3\\n\",\n        \"output\": \" Yes, Tm2Ga10Os3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd2ZnGa\\n\",\n        \"output\": \" Yes, Nd2ZnGa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr4Co4Ge7\\n\",\n        \"output\": \" Yes, Zr4Co4Ge7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrTi2O\\n\",\n        \"output\": \" Yes, ZrTi2O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb(AlC)3\\n\",\n        \"output\": \" Yes, Tb(AlC)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KSnAuSe3\\n\",\n        \"output\": \" No, KSnAuSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2In2GeS6\\n\",\n        \"output\": \" No, Li2In2GeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce3SiPt5\\n\",\n        \"output\": \" Yes, Ce3SiPt5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" needle\\n\",\n        \"output\": \" needle is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2MnCo3O8\\n\",\n        \"output\": \" Yes, Li2MnCo3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaGe3Pt\\n\",\n        \"output\": \" Yes, BaGe3Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.99Ga0.01As0.01P0.99\\n\",\n        \"output\": \" No, In0.99Ga0.01As0.01P0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn2BiS2I3\\n\",\n        \"output\": \" No, Sn2BiS2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiInSe2\\n\",\n        \"output\": \" No, LiInSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li5Co2O2F5\\n\",\n        \"output\": \" Yes, Li5Co2O2F5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NiP2\\n\",\n        \"output\": \" No, NiP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiGaPd2\\n\",\n        \"output\": \" Yes, LiGaPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgBiPbS3\\n\",\n        \"output\": \" No, AgBiPbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu2GeSe3\\n\",\n        \"output\": \" No, Cu2GeSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3CaIr2O9\\n\",\n        \"output\": \" Yes, Ba3CaIr2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaN\\n\",\n        \"output\": \" No, GaN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Er5Bi3\\n\",\n        \"output\": \" Yes, Er5Bi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KThCuS3\\n\",\n        \"output\": \" No, KThCuS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VO\\n\",\n        \"output\": \" No, VO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" H6Pt(I3O10)2\\n\",\n        \"output\": \" No, H6Pt(I3O10)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pm2CuGe\\n\",\n        \"output\": \" Yes, Pm2CuGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc3PbC\\n\",\n        \"output\": \" Yes, Sc3PbC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrMo3\\n\",\n        \"output\": \" Yes, ZrMo3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbI\\n\",\n        \"output\": \" No, RbI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu5(Si2O7)2\\n\",\n        \"output\": \" Yes, Cu5(Si2O7)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs4BiAs3Se7\\n\",\n        \"output\": \" No, Cs4BiAs3Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScTlTe2\\n\",\n        \"output\": \" No, ScTlTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr7Bi23O40\\n\",\n        \"output\": \" Yes, Sr7Bi23O40 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl16O15F17\\n\",\n        \"output\": \" Yes, Tl16O15F17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr3Sb2\\n\",\n        \"output\": \" Yes, Sr3Sb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NbHO3\\n\",\n        \"output\": \" Yes, NbHO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnO\\n\",\n        \"output\": \" No, ZnO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In2HgSe4\\n\",\n        \"output\": \" No, In2HgSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaLa2In2Se7\\n\",\n        \"output\": \" No, BaLa2In2Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NbHg3F6\\n\",\n        \"output\": \" Yes, NbHg3F6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiCa3As2H\\n\",\n        \"output\": \" No, LiCa3As2H is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KFe2BiO5\\n\",\n        \"output\": \" No, KFe2BiO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc6FeSb2\\n\",\n        \"output\": \" Yes, Sc6FeSb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd2HfS5\\n\",\n        \"output\": \" No, Nd2HfS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CrB2(PbO2)6\\n\",\n        \"output\": \" No, CrB2(PbO2)6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" kettledrum\\n\",\n        \"output\": \" kettledrum is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.6Cu0.4S2.6\\n\",\n        \"output\": \" No, Ga1.6Cu0.4S2.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaY(Te2O5)2\\n\",\n        \"output\": \" No, NaY(Te2O5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsEr9(Cd2Se9)2\\n\",\n        \"output\": \" No, CsEr9(Cd2Se9)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgSbPt\\n\",\n        \"output\": \" Yes, MgSbPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AsSeI\\n\",\n        \"output\": \" No, AsSeI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuTiO3\\n\",\n        \"output\": \" Yes, EuTiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" chief\\n\",\n        \"output\": \" chief is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsPSe4\\n\",\n        \"output\": \" No, CsPSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu3Bi4S9\\n\",\n        \"output\": \" No, Eu3Bi4S9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YCu3(WO3)4\\n\",\n        \"output\": \" Yes, YCu3(WO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaHg\\n\",\n        \"output\": \" Yes, LaHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaMg2H7Pd\\n\",\n        \"output\": \" No, LaMg2H7Pd is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li15(FeO4)4\\n\",\n        \"output\": \" Yes, Li15(FeO4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba6In2NF\\n\",\n        \"output\": \" Yes, Ba6In2NF is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BSbPbS4\\n\",\n        \"output\": \" No, BSbPbS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2InSbSe5\\n\",\n        \"output\": \" No, Ba2InSbSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbTlS2\\n\",\n        \"output\": \" Yes, YbTlS2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaNO2\\n\",\n        \"output\": \" No, NaNO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThHg2\\n\",\n        \"output\": \" Yes, ThHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbB2Rh3\\n\",\n        \"output\": \" Yes, YbB2Rh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeHg\\n\",\n        \"output\": \" Yes, CeHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Th(FeSi)2\\n\",\n        \"output\": \" Yes, Th(FeSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi1.98Sb0.02Te3\\n\",\n        \"output\": \" No, Bi1.98Sb0.02Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hg7.5As4Cl6\\n\",\n        \"output\": \" No, Hg7.5As4Cl6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnGaRh2\\n\",\n        \"output\": \" Yes, ZnGaRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErNiSn\\n\",\n        \"output\": \" Yes, ErNiSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ErTlPd\\n\",\n        \"output\": \" Yes, ErTlPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc2O3\\n\",\n        \"output\": \" No, Sc2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PmMgRh2\\n\",\n        \"output\": \" Yes, PmMgRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb2In16Pt7\\n\",\n        \"output\": \" Yes, Tb2In16Pt7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1.6Ga0.4Cu1S3.5\\n\",\n        \"output\": \" No, In1.6Ga0.4Cu1S3.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuCl\\n\",\n        \"output\": \" No, CuCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd(InTe2)2\\n\",\n        \"output\": \" No, Cd(InTe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdP2\\n\",\n        \"output\": \" No, CdP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2NdSb2\\n\",\n        \"output\": \" Yes, Li2NdSb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu3Ga\\n\",\n        \"output\": \" Yes, Lu3Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb(InS2)3\\n\",\n        \"output\": \" No, Yb(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VBi24O41\\n\",\n        \"output\": \" No, VBi24O41 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Er(ReO4)2\\n\",\n        \"output\": \" Yes, Er(ReO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" tent\\n\",\n        \"output\": \" tent is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si2Ni6B\\n\",\n        \"output\": \" Yes, Si2Ni6B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrGe2\\n\",\n        \"output\": \" Yes, ZrGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Mn(CuO3)2\\n\",\n        \"output\": \" Yes, Li3Mn(CuO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiPd\\n\",\n        \"output\": \" Yes, TiPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgSO4\\n\",\n        \"output\": \" No, AgSO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ErSnAu\\n\",\n        \"output\": \" Yes, ErSnAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Er3SnC\\n\",\n        \"output\": \" Yes, Er3SnC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr5Sn3\\n\",\n        \"output\": \" Yes, Zr5Sn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnGaNi2\\n\",\n        \"output\": \" Yes, MnGaNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Hg6S7\\n\",\n        \"output\": \" No, Cs2Hg6S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbYbRh2\\n\",\n        \"output\": \" Yes, TbYbRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiMn2Ge\\n\",\n        \"output\": \" Yes, TiMn2Ge is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyRh\\n\",\n        \"output\": \" Yes, DyRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho3Ge5\\n\",\n        \"output\": \" Yes, Ho3Ge5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce3Ta(ClO2)3\\n\",\n        \"output\": \" Yes, Ce3Ta(ClO2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Gd1Mn1.95In1.05S5\\n\",\n        \"output\": \" No, Gd1Mn1.95In1.05S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuMoO4\\n\",\n        \"output\": \" Yes, CuMoO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1.1Cu0.9Se2.1\\n\",\n        \"output\": \" No, In1.1Cu0.9Se2.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta2TiN3\\n\",\n        \"output\": \" Yes, Ta2TiN3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.1Sb0.9Te0.3\\n\",\n        \"output\": \" No, Ga1.1Sb0.9Te0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsSbTe2\\n\",\n        \"output\": \" No, CsSbTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbSc(SeO3)2\\n\",\n        \"output\": \" No, RbSc(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti2BRh6\\n\",\n        \"output\": \" Yes, Ti2BRh6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiAl3\\n\",\n        \"output\": \" Yes, LiAl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K(FeAs)2\\n\",\n        \"output\": \" Yes, K(FeAs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiCoSb\\n\",\n        \"output\": \" No, TiCoSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaAgF5\\n\",\n        \"output\": \" Yes, CaAgF5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HgBrCl\\n\",\n        \"output\": \" No, HgBrCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4VF7\\n\",\n        \"output\": \" Yes, Li4VF7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd4MgRu\\n\",\n        \"output\": \" Yes, Nd4MgRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BiSBr\\n\",\n        \"output\": \" No, BiSBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnHg3(SeCl2)2\\n\",\n        \"output\": \" No, ZnHg3(SeCl2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaSi\\n\",\n        \"output\": \" Yes, BaSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaSb\\n\",\n        \"output\": \" No, NaSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnB12(H5O12)2\\n\",\n        \"output\": \" No, ZnB12(H5O12)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.2Ga0.8P1\\n\",\n        \"output\": \" No, Al0.2Ga0.8P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd3Al0.74Si0.7S7\\n\",\n        \"output\": \" No, Gd3Al0.74Si0.7S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr2(Co7B2)3\\n\",\n        \"output\": \" Yes, Zr2(Co7B2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2CdGeS4\\n\",\n        \"output\": \" No, Li2CdGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr2Co12P7\\n\",\n        \"output\": \" Yes, Pr2Co12P7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiZn(Fe5O8)2\\n\",\n        \"output\": \" Yes, LiZn(Fe5O8)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn3Cu\\n\",\n        \"output\": \" Yes, Zn3Cu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te0.05Pb1Se0.95\\n\",\n        \"output\": \" No, Te0.05Pb1Se0.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Ga3CuSe6\\n\",\n        \"output\": \" No, K2Ga3CuSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" P2Ru\\n\",\n        \"output\": \" No, P2Ru is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd2ZrS5\\n\",\n        \"output\": \" No, Nd2ZrS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.3In0.7P1\\n\",\n        \"output\": \" No, Al0.3In0.7P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce4FeSe6O\\n\",\n        \"output\": \" Yes, Ce4FeSe6O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KAg2SbS3\\n\",\n        \"output\": \" No, KAg2SbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca3Au4\\n\",\n        \"output\": \" Yes, Ca3Au4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc2CuRu\\n\",\n        \"output\": \" Yes, Sc2CuRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr4AlNi2\\n\",\n        \"output\": \" Yes, Zr4AlNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb15Hg16\\n\",\n        \"output\": \" Yes, Rb15Hg16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrCo4B\\n\",\n        \"output\": \" Yes, PrCo4B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Co5RuO8\\n\",\n        \"output\": \" Yes, Co5RuO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.8Ga0.2As0.8P0.2\\n\",\n        \"output\": \" No, In0.8Ga0.2As0.8P0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" V3CuO8\\n\",\n        \"output\": \" Yes, V3CuO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2TeBr6\\n\",\n        \"output\": \" No, Cs2TeBr6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeZnPO\\n\",\n        \"output\": \" Yes, CeZnPO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrP\\n\",\n        \"output\": \" Yes, PrP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlNi2\\n\",\n        \"output\": \" Yes, AlNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmLuPd2\\n\",\n        \"output\": \" Yes, TmLuPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2La2Ti3O10\\n\",\n        \"output\": \" No, K2La2Ti3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrGeAu\\n\",\n        \"output\": \" Yes, PrGeAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.85Ga0.15P0.15S0.85\\n\",\n        \"output\": \" No, Zn0.85Ga0.15P0.15S0.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaTlS3\\n\",\n        \"output\": \" No, TaTlS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlGaTe2\\n\",\n        \"output\": \" No, TlGaTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr(CoGe)2\\n\",\n        \"output\": \" Yes, Pr(CoGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi12PO20\\n\",\n        \"output\": \" No, Bi12PO20 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" paint\\n\",\n        \"output\": \" paint is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2S3\\n\",\n        \"output\": \" No, La2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UO2\\n\",\n        \"output\": \" No, UO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf2MnIr\\n\",\n        \"output\": \" Yes, Hf2MnIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2(PPt2)3\\n\",\n        \"output\": \" Yes, Sm2(PPt2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2(MoO4)3\\n\",\n        \"output\": \" No, Bi2(MoO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NbCrW\\n\",\n        \"output\": \" Yes, NbCrW is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li0.33Ti0.67Ag1O2\\n\",\n        \"output\": \" No, Li0.33Ti0.67Ag1O2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" No, Na0.5Ge1Pb1.75S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Cd3Te4\\n\",\n        \"output\": \" No, K2Cd3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn3P3O13\\n\",\n        \"output\": \" Yes, Sn3P3O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Er3Te4\\n\",\n        \"output\": \" No, Er3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HgPt\\n\",\n        \"output\": \" Yes, HgPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbAg2TeS6\\n\",\n        \"output\": \" No, RbAg2TeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu11Sb4S13\\n\",\n        \"output\": \" Yes, Cu11Sb4S13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" kale\\n\",\n        \"output\": \" kale is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeMgZn2\\n\",\n        \"output\": \" Yes, CeMgZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3(Cu4S3)2\\n\",\n        \"output\": \" Yes, Rb3(Cu4S3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li0.33Ag1Sn0.67O2\\n\",\n        \"output\": \" No, Li0.33Ag1Sn0.67O2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl2CdTe4\\n\",\n        \"output\": \" Yes, Tl2CdTe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaYbSn3\\n\",\n        \"output\": \" Yes, BaYbSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga5Ge(PbSe3)4\\n\",\n        \"output\": \" No, Ga5Ge(PbSe3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrC\\n\",\n        \"output\": \" No, ZrC is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy(GeRu)2\\n\",\n        \"output\": \" Yes, Dy(GeRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiMn9Se10\\n\",\n        \"output\": \" Yes, LiMn9Se10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaUSe3\\n\",\n        \"output\": \" No, BaUSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3V2(SeO4)4\\n\",\n        \"output\": \" No, Ba3V2(SeO4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaI2\\n\",\n        \"output\": \" No, CaI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In2Pt\\n\",\n        \"output\": \" Yes, In2Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdO2\\n\",\n        \"output\": \" Yes, NdO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdI2\\n\",\n        \"output\": \" No, CdI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3P3ClO10\\n\",\n        \"output\": \" No, Ba3P3ClO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg2RhAu\\n\",\n        \"output\": \" Yes, Mg2RhAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiNiSb\\n\",\n        \"output\": \" No, TiNiSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbCl\\n\",\n        \"output\": \" No, RbCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hf2S\\n\",\n        \"output\": \" Yes, Hf2S is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd(InS2)3\\n\",\n        \"output\": \" No, Nd(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Si15(TeP2)4\\n\",\n        \"output\": \" No, Si15(TeP2)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy2Ti3Si4\\n\",\n        \"output\": \" Yes, Dy2Ti3Si4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" U3Cu2Se7\\n\",\n        \"output\": \" Yes, U3Cu2Se7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb2MgSe4\\n\",\n        \"output\": \" Yes, Yb2MgSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SnI4\\n\",\n        \"output\": \" No, SnI4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrSe3\\n\",\n        \"output\": \" No, ZrSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" V2Sb(PO4)3\\n\",\n        \"output\": \" Yes, V2Sb(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf5Sn4\\n\",\n        \"output\": \" Yes, Hf5Sn4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsInI3\\n\",\n        \"output\": \" Yes, CsInI3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi4I\\n\",\n        \"output\": \" Yes, Bi4I is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Nb2AsSe11\\n\",\n        \"output\": \" No, Rb3Nb2AsSe11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg3Bi2\\n\",\n        \"output\": \" Yes, Mg3Bi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li6Fe3Co7O20\\n\",\n        \"output\": \" Yes, Li6Fe3Co7O20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu(NiAs)2\\n\",\n        \"output\": \" Yes, Eu(NiAs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1Sb0.99As0.01\\n\",\n        \"output\": \" No, In1Sb0.99As0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CoP3\\n\",\n        \"output\": \" No, CoP3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K3Ta2AsS11\\n\",\n        \"output\": \" No, K3Ta2AsS11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" snake\\n\",\n        \"output\": \" snake is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd(Re2Si)2\\n\",\n        \"output\": \" Yes, Nd(Re2Si)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2TeBr6\\n\",\n        \"output\": \" No, Rb2TeBr6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrZnSO\\n\",\n        \"output\": \" No, SrZnSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn5.5Ga1Sn0.5O8\\n\",\n        \"output\": \" No, Zn5.5Ga1Sn0.5O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdCl2\\n\",\n        \"output\": \" No, CdCl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd5Ge4\\n\",\n        \"output\": \" Yes, Nd5Ge4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Zn(BO2)5\\n\",\n        \"output\": \" No, Rb3Zn(BO2)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La(InS2)3\\n\",\n        \"output\": \" No, La(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlCr5(Se3S)2\\n\",\n        \"output\": \" No, TlCr5(Se3S)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KP(HO2)2\\n\",\n        \"output\": \" No, KP(HO2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs3PW3O13\\n\",\n        \"output\": \" No, Cs3PW3O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu3As2\\n\",\n        \"output\": \" No, Eu3As2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y(NiP)2\\n\",\n        \"output\": \" Yes, Y(NiP)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr2S3\\n\",\n        \"output\": \" No, Cr2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.3Ga0.7As1\\n\",\n        \"output\": \" No, In0.3Ga0.7As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba(AsRh)2\\n\",\n        \"output\": \" Yes, Ba(AsRh)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu5(Si5Ir2)2\\n\",\n        \"output\": \" Yes, Lu5(Si5Ir2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Be2HgTe\\n\",\n        \"output\": \" Yes, Be2HgTe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeSI\\n\",\n        \"output\": \" Yes, CeSI is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V2Zn3TeO10\\n\",\n        \"output\": \" No, V2Zn3TeO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd3.04Sc0.96S6\\n\",\n        \"output\": \" No, Gd3.04Sc0.96S6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaAg2\\n\",\n        \"output\": \" Yes, BaAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr(NdS2)2\\n\",\n        \"output\": \" No, Sr(NdS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd2(Zn2Ge)3\\n\",\n        \"output\": \" Yes, Gd2(Zn2Ge)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y4AsSe3\\n\",\n        \"output\": \" Yes, Y4AsSe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" planet\\n\",\n        \"output\": \" planet is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y3GaCo3\\n\",\n        \"output\": \" Yes, Y3GaCo3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2ZnSe3\\n\",\n        \"output\": \" No, Ba2ZnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Mn3WO8\\n\",\n        \"output\": \" Yes, Li3Mn3WO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BTe2As\\n\",\n        \"output\": \" Yes, BTe2As is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag3SbS3\\n\",\n        \"output\": \" No, Ag3SbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaTc\\n\",\n        \"output\": \" No, GaTc is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi0.002Te0.003Pb0.999Se0.999\\n\",\n        \"output\": \" No, Bi0.002Te0.003Pb0.999Se0.999 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In3Bi7(Pb2S9)2\\n\",\n        \"output\": \" Yes, In3Bi7(Pb2S9)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2Ge\\n\",\n        \"output\": \" No, Ca2Ge is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgS\\n\",\n        \"output\": \" No, AgS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd3Te2MoO10\\n\",\n        \"output\": \" No, Cd3Te2MoO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCaBO3\\n\",\n        \"output\": \" No, CsCaBO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KTi5Se8\\n\",\n        \"output\": \" Yes, KTi5Se8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K0.8Sn2Hg1.2S8\\n\",\n        \"output\": \" No, K0.8Sn2Hg1.2S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgCuSb\\n\",\n        \"output\": \" Yes, MgCuSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Cd2Te3\\n\",\n        \"output\": \" No, K2Cd2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiNiP2O7\\n\",\n        \"output\": \" Yes, LiNiP2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.4Ga1.6Cu1S3.5\\n\",\n        \"output\": \" No, In0.4Ga1.6Cu1S3.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2In2Se5\\n\",\n        \"output\": \" No, Ba2In2Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb6Pb6Se17\\n\",\n        \"output\": \" No, Sb6Pb6Se17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In3Pd5\\n\",\n        \"output\": \" Yes, In3Pd5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Dy2Ti3O10\\n\",\n        \"output\": \" No, K2Dy2Ti3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm2In\\n\",\n        \"output\": \" Yes, Tm2In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2ZnGe3S8\\n\",\n        \"output\": \" No, Cs2ZnGe3S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na3MoO4F\\n\",\n        \"output\": \" No, Na3MoO4F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba5(Ga2Se5)2\\n\",\n        \"output\": \" No, Ba5(Ga2Se5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.28Hg0.72Te1\\n\",\n        \"output\": \" No, Cd0.28Hg0.72Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.55Ga0.45P0.45S0.55\\n\",\n        \"output\": \" No, Zn0.55Ga0.45P0.45S0.55 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr3(Cu2Si3)2\\n\",\n        \"output\": \" Yes, Zr3(Cu2Si3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbGa2Co3\\n\",\n        \"output\": \" Yes, TbGa2Co3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Ni3(PO4)4\\n\",\n        \"output\": \" Yes, Li3Ni3(PO4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoZnRh\\n\",\n        \"output\": \" Yes, HoZnRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta2N\\n\",\n        \"output\": \" Yes, Ta2N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuCuSeO\\n\",\n        \"output\": \" Yes, EuCuSeO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd2AlCo2\\n\",\n        \"output\": \" Yes, Gd2AlCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsRb(PSe4)2\\n\",\n        \"output\": \" No, CsRb(PSe4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.25Te1Pb0.75\\n\",\n        \"output\": \" No, Ge0.25Te1Pb0.75 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U2Zn17\\n\",\n        \"output\": \" Yes, U2Zn17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl5Te3\\n\",\n        \"output\": \" Yes, Tl5Te3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu3AsSe4\\n\",\n        \"output\": \" No, Cu3AsSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdHg4(AsI2)2\\n\",\n        \"output\": \" No, CdHg4(AsI2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaSiRu2\\n\",\n        \"output\": \" Yes, GaSiRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" pink\\n\",\n        \"output\": \" pink is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" twist\\n\",\n        \"output\": \" twist is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.3Ga0.7As0.7P0.3\\n\",\n        \"output\": \" No, In0.3Ga0.7As0.7P0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Fe3NiO8\\n\",\n        \"output\": \" Yes, Li4Fe3NiO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BiSeO3F\\n\",\n        \"output\": \" No, BiSeO3F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiI\\n\",\n        \"output\": \" No, LiI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2V2(SeO5)3\\n\",\n        \"output\": \" No, Sr2V2(SeO5)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaAl4\\n\",\n        \"output\": \" Yes, LaAl4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2Se\\n\",\n        \"output\": \" No, In2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiCu3F7\\n\",\n        \"output\": \" Yes, LiCu3F7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd1Se0.35S0.65\\n\",\n        \"output\": \" No, Cd1Se0.35S0.65 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr3Bi(PO4)3\\n\",\n        \"output\": \" No, Sr3Bi(PO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg2Pb\\n\",\n        \"output\": \" No, Mg2Pb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho2Au\\n\",\n        \"output\": \" Yes, Ho2Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiAlB14\\n\",\n        \"output\": \" No, LiAlB14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr3O\\n\",\n        \"output\": \" No, Zr3O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La4InSbS9\\n\",\n        \"output\": \" No, La4InSbS9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" outrigger\\n\",\n        \"output\": \" outrigger is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdIn8Te13\\n\",\n        \"output\": \" No, CdIn8Te13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2La2Sb2S9\\n\",\n        \"output\": \" No, K2La2Sb2S9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BH(PbO2)2\\n\",\n        \"output\": \" No, BH(PbO2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2TeBr6\\n\",\n        \"output\": \" No, Tl2TeBr6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiTi3O6\\n\",\n        \"output\": \" Yes, LiTi3O6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm(CuGe)2\\n\",\n        \"output\": \" Yes, Tm(CuGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" FeSi2\\n\",\n        \"output\": \" No, FeSi2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V6AgO15\\n\",\n        \"output\": \" Yes, V6AgO15 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScZnPt2\\n\",\n        \"output\": \" Yes, ScZnPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbAs\\n\",\n        \"output\": \" No, YbAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuSnAu2\\n\",\n        \"output\": \" Yes, EuSnAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsGa7\\n\",\n        \"output\": \" Yes, CsGa7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuClO2\\n\",\n        \"output\": \" Yes, CuClO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr1.29Lu0.71S3\\n\",\n        \"output\": \" No, Pr1.29Lu0.71S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" billboard\\n\",\n        \"output\": \" billboard is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KRuO4\\n\",\n        \"output\": \" Yes, KRuO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KTiPO5\\n\",\n        \"output\": \" No, KTiPO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr1Te1.9\\n\",\n        \"output\": \" No, Pr1Te1.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag2GeSe3\\n\",\n        \"output\": \" No, Ag2GeSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb3B2\\n\",\n        \"output\": \" Yes, Nb3B2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2PbAu2\\n\",\n        \"output\": \" Yes, Ca2PbAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaAl4Co\\n\",\n        \"output\": \" Yes, LaAl4Co is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1As0.7P0.3\\n\",\n        \"output\": \" No, Ga1As0.7P0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiV4CuO12\\n\",\n        \"output\": \" Yes, TiV4CuO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho2S3\\n\",\n        \"output\": \" No, Ho2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CrO2\\n\",\n        \"output\": \" No, CrO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi2SI2O11\\n\",\n        \"output\": \" No, Bi2SI2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1Sb0.14As0.86\\n\",\n        \"output\": \" No, Ga1Sb0.14As0.86 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg3(MnAl9)2\\n\",\n        \"output\": \" Yes, Mg3(MnAl9)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y4GaSbS9\\n\",\n        \"output\": \" No, Y4GaSbS9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrAgAs2\\n\",\n        \"output\": \" Yes, PrAgAs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1As0.3P0.7\\n\",\n        \"output\": \" No, Ga1As0.3P0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaReB\\n\",\n        \"output\": \" Yes, LaReB is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiCu2Ge\\n\",\n        \"output\": \" Yes, LiCu2Ge is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GdCd4B3O10\\n\",\n        \"output\": \" No, GdCd4B3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Te2Os\\n\",\n        \"output\": \" No, Te2Os is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti2ReRu\\n\",\n        \"output\": \" Yes, Ti2ReRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SbOsSe\\n\",\n        \"output\": \" No, SbOsSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbWClO4\\n\",\n        \"output\": \" No, YbWClO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb2Sb5\\n\",\n        \"output\": \" Yes, Tb2Sb5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KNb2Se\\n\",\n        \"output\": \" Yes, KNb2Se is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.41Te1Pb0.59\\n\",\n        \"output\": \" No, Ge0.41Te1Pb0.59 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmMgHg2\\n\",\n        \"output\": \" Yes, SmMgHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Pt(IO3)6\\n\",\n        \"output\": \" No, Cs2Pt(IO3)6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdScGe\\n\",\n        \"output\": \" Yes, NdScGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba6Al4B14O33\\n\",\n        \"output\": \" No, Ba6Al4B14O33 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" market\\n\",\n        \"output\": \" market is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbWO3\\n\",\n        \"output\": \" Yes, RbWO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Be22Re\\n\",\n        \"output\": \" Yes, Be22Re is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiI\\n\",\n        \"output\": \" Yes, TiI is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrLuIn2\\n\",\n        \"output\": \" Yes, PrLuIn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb2(ZnGe)3\\n\",\n        \"output\": \" Yes, Yb2(ZnGe)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThSO\\n\",\n        \"output\": \" No, ThSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4Ge3Se9Cl2\\n\",\n        \"output\": \" No, Ba4Ge3Se9Cl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr2MgIrO6\\n\",\n        \"output\": \" Yes, Sr2MgIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd(AsPd)2\\n\",\n        \"output\": \" Yes, Nd(AsPd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfTl3\\n\",\n        \"output\": \" Yes, HfTl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb3Si\\n\",\n        \"output\": \" Yes, Tb3Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnGePd\\n\",\n        \"output\": \" Yes, MnGePd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(CdSb)2\\n\",\n        \"output\": \" Yes, Eu(CdSb)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba(InS2)2\\n\",\n        \"output\": \" No, Ba(InS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2DyIn\\n\",\n        \"output\": \" Yes, Li2DyIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PdS\\n\",\n        \"output\": \" No, PdS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y2Ru2O7\\n\",\n        \"output\": \" Yes, Y2Ru2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb2AlCo2\\n\",\n        \"output\": \" Yes, Tb2AlCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu2Sb\\n\",\n        \"output\": \" Yes, Cu2Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaBi3\\n\",\n        \"output\": \" Yes, NaBi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U2Re2C3\\n\",\n        \"output\": \" Yes, U2Re2C3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb7Th2(P2Se7)3\\n\",\n        \"output\": \" No, Rb7Th2(P2Se7)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag2GeTe3\\n\",\n        \"output\": \" No, Ag2GeTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmSnTe2\\n\",\n        \"output\": \" No, SmSnTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaGe4(IrS3)2\\n\",\n        \"output\": \" No, BaGe4(IrS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" DyB2Rh2C\\n\",\n        \"output\": \" Yes, DyB2Rh2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er5Si3\\n\",\n        \"output\": \" Yes, Er5Si3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf3(CuSi)4\\n\",\n        \"output\": \" Yes, Hf3(CuSi)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1.5Cu0.5Se2.5\\n\",\n        \"output\": \" No, In1.5Cu0.5Se2.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CoP2\\n\",\n        \"output\": \" No, CoP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgSe\\n\",\n        \"output\": \" No, MgSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.01Ga0.99Sb0.99Te0.01\\n\",\n        \"output\": \" No, Cd0.01Ga0.99Sb0.99Te0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge2Sb2Te5\\n\",\n        \"output\": \" No, Ge2Sb2Te5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl4CdI6\\n\",\n        \"output\": \" No, Tl4CdI6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeTl2P2S7\\n\",\n        \"output\": \" No, CeTl2P2S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ReSn3\\n\",\n        \"output\": \" Yes, ReSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.1Pb0.9Se0.9S0.1\\n\",\n        \"output\": \" No, Ge0.1Pb0.9Se0.9S0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuBS2\\n\",\n        \"output\": \" No, CuBS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaBiS2\\n\",\n        \"output\": \" No, NaBiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga4SnS7\\n\",\n        \"output\": \" No, Ga4SnS7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba4Ge3S9Cl2\\n\",\n        \"output\": \" No, Ba4Ge3S9Cl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiCoGe\\n\",\n        \"output\": \" Yes, TiCoGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li4NbNi3O8\\n\",\n        \"output\": \" Yes, Li4NbNi3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4Ga5Si18\\n\",\n        \"output\": \" No, Ba4Ga5Si18 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2TeMoO6\\n\",\n        \"output\": \" No, Li2TeMoO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaTbMn2O6\\n\",\n        \"output\": \" Yes, BaTbMn2O6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sb6Pb4Se13\\n\",\n        \"output\": \" No, Sb6Pb4Se13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaAs2W\\n\",\n        \"output\": \" Yes, GaAs2W is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaGaGe3Se8\\n\",\n        \"output\": \" No, NaGaGe3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" astronomy\\n\",\n        \"output\": \" astronomy is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnTe\\n\",\n        \"output\": \" No, ZnTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.3Hg0.7Te1\\n\",\n        \"output\": \" No, Cd0.3Hg0.7Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaCu5\\n\",\n        \"output\": \" Yes, CaCu5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KCu3S2\\n\",\n        \"output\": \" No, KCu3S2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaAgGe5Se12\\n\",\n        \"output\": \" No, GaAgGe5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScBIr3\\n\",\n        \"output\": \" Yes, ScBIr3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu2FeS4\\n\",\n        \"output\": \" Yes, Lu2FeS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CrNi3\\n\",\n        \"output\": \" Yes, CrNi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuBPd3\\n\",\n        \"output\": \" Yes, LuBPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba5Sb3\\n\",\n        \"output\": \" Yes, Ba5Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HfSi\\n\",\n        \"output\": \" Yes, HfSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd2PbO4\\n\",\n        \"output\": \" Yes, Cd2PbO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.85Ga0.15As0.15Se0.85\\n\",\n        \"output\": \" No, Zn0.85Ga0.15As0.15Se0.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U(Al2Fe)4\\n\",\n        \"output\": \" Yes, U(Al2Fe)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1As0.1P0.9\\n\",\n        \"output\": \" No, Ga1As0.1P0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga9Rh2\\n\",\n        \"output\": \" Yes, Ga9Rh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaCeS3\\n\",\n        \"output\": \" No, NaCeS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" kitty\\n\",\n        \"output\": \" kitty is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn(CoO2)2\\n\",\n        \"output\": \" Yes, Zn(CoO2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" step-sister\\n\",\n        \"output\": \" step-sister is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InFe2CuSe4\\n\",\n        \"output\": \" Yes, InFe2CuSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaTa3\\n\",\n        \"output\": \" Yes, NaTa3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrTe2\\n\",\n        \"output\": \" No, PrTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KAgAsS2\\n\",\n        \"output\": \" No, KAgAsS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KBi3S5\\n\",\n        \"output\": \" No, KBi3S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdGaO3\\n\",\n        \"output\": \" Yes, NdGaO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2Pr2Pt1O7.07\\n\",\n        \"output\": \" No, Sr2Pr2Pt1O7.07 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2ScIrO6\\n\",\n        \"output\": \" Yes, Ba2ScIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsMn4In5Te12\\n\",\n        \"output\": \" No, CsMn4In5Te12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaZn5\\n\",\n        \"output\": \" Yes, CaZn5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn3PtN\\n\",\n        \"output\": \" Yes, Mn3PtN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeMgAg2\\n\",\n        \"output\": \" Yes, CeMgAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb3IrSe8\\n\",\n        \"output\": \" Yes, Nb3IrSe8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiBPbO4\\n\",\n        \"output\": \" No, BiBPbO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li11Mn13O32\\n\",\n        \"output\": \" Yes, Li11Mn13O32 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KNb3(SeO6)2\\n\",\n        \"output\": \" No, KNb3(SeO6)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BeS\\n\",\n        \"output\": \" No, BeS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiLu2Ru\\n\",\n        \"output\": \" Yes, LiLu2Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" P2Os\\n\",\n        \"output\": \" No, P2Os is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2In\\n\",\n        \"output\": \" Yes, Na2In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NbCuO3\\n\",\n        \"output\": \" No, NbCuO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(MnAs)2\\n\",\n        \"output\": \" Yes, Ca(MnAs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.37Hg0.63Te1\\n\",\n        \"output\": \" No, Cd0.37Hg0.63Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4.5Cr0.5Te1O6\\n\",\n        \"output\": \" No, Li4.5Cr0.5Te1O6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CI4\\n\",\n        \"output\": \" No, CI4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScCu2\\n\",\n        \"output\": \" Yes, ScCu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CoSb3\\n\",\n        \"output\": \" No, CoSb3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Ti2Sb2O\\n\",\n        \"output\": \" Yes, Na2Ti2Sb2O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1Sb0.85As0.15\\n\",\n        \"output\": \" No, Ga1Sb0.85As0.15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlTeP\\n\",\n        \"output\": \" No, TlTeP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgCr\\n\",\n        \"output\": \" Yes, MgCr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgCNO\\n\",\n        \"output\": \" Yes, AgCNO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" swing\\n\",\n        \"output\": \" swing is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm(GeRu)2\\n\",\n        \"output\": \" Yes, Tm(GeRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb16S29\\n\",\n        \"output\": \" Yes, Yb16S29 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2NiS4\\n\",\n        \"output\": \" Yes, Ga2NiS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr3(SnIr)4\\n\",\n        \"output\": \" Yes, Sr3(SnIr)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs3Bi\\n\",\n        \"output\": \" No, Cs3Bi is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In2O3\\n\",\n        \"output\": \" No, In2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaSi2Ru\\n\",\n        \"output\": \" Yes, LaSi2Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsPSe6\\n\",\n        \"output\": \" No, CsPSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KLi(WO3)3\\n\",\n        \"output\": \" Yes, KLi(WO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InAs\\n\",\n        \"output\": \" No, InAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VZnRu2\\n\",\n        \"output\": \" Yes, VZnRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlN3\\n\",\n        \"output\": \" No, TlN3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GdAs\\n\",\n        \"output\": \" No, GdAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi0.6Sb1.4Te3\\n\",\n        \"output\": \" No, Bi0.6Sb1.4Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaZn3Ni2\\n\",\n        \"output\": \" Yes, CaZn3Ni2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaFeNi2\\n\",\n        \"output\": \" Yes, GaFeNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbBiS2\\n\",\n        \"output\": \" No, RbBiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K3NaSn3Se8\\n\",\n        \"output\": \" No, K3NaSn3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Dy2(PS4)4\\n\",\n        \"output\": \" No, Ba3Dy2(PS4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu(IrS2)2\\n\",\n        \"output\": \" Yes, Cu(IrS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga4PbS7\\n\",\n        \"output\": \" No, Ga4PbS7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.1Sb0.9Se0.3\\n\",\n        \"output\": \" No, Ga1.1Sb0.9Se0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2PAuS4\\n\",\n        \"output\": \" No, K2PAuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.23Te1Pb0.77\\n\",\n        \"output\": \" No, Sn0.23Te1Pb0.77 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga0.04Te1Pb0.96\\n\",\n        \"output\": \" No, Ga0.04Te1Pb0.96 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al2Te3\\n\",\n        \"output\": \" No, Al2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrCd\\n\",\n        \"output\": \" Yes, PrCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr27Se40\\n\",\n        \"output\": \" Yes, Pr27Se40 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3YIr2O9\\n\",\n        \"output\": \" Yes, Ba3YIr2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmSb\\n\",\n        \"output\": \" Yes, TmSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb(HO)3\\n\",\n        \"output\": \" Yes, Yb(HO)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2PrP2\\n\",\n        \"output\": \" Yes, Li2PrP2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaHSeO4\\n\",\n        \"output\": \" No, GaHSeO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.5In0.5P1\\n\",\n        \"output\": \" No, Al0.5In0.5P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn0.05Te1Pb0.95\\n\",\n        \"output\": \" No, Mn0.05Te1Pb0.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag2O\\n\",\n        \"output\": \" No, Ag2O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y(CrSi)2\\n\",\n        \"output\": \" Yes, Y(CrSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg(FeS2)2\\n\",\n        \"output\": \" Yes, Mg(FeS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb(GeRh)2\\n\",\n        \"output\": \" Yes, Tb(GeRh)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlFe2Si\\n\",\n        \"output\": \" Yes, AlFe2Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce4Bi3\\n\",\n        \"output\": \" Yes, Ce4Bi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pd2N\\n\",\n        \"output\": \" Yes, Pd2N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrLi2Sn\\n\",\n        \"output\": \" Yes, SrLi2Sn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsMnSb\\n\",\n        \"output\": \" Yes, CsMnSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc(VGa2)2\\n\",\n        \"output\": \" Yes, Sc(VGa2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er2(MoO4)3\\n\",\n        \"output\": \" No, Er2(MoO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na11Ti20O40\\n\",\n        \"output\": \" Yes, Na11Ti20O40 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" V12P7\\n\",\n        \"output\": \" Yes, V12P7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.15Cd0.85Se1\\n\",\n        \"output\": \" No, Zn0.15Cd0.85Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiLa2IrO6\\n\",\n        \"output\": \" Yes, LiLa2IrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb3Tc\\n\",\n        \"output\": \" Yes, Yb3Tc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu9O13\\n\",\n        \"output\": \" Yes, Cu9O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsSmZnSe3\\n\",\n        \"output\": \" No, CsSmZnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgInPd2\\n\",\n        \"output\": \" Yes, MgInPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaBSbS4\\n\",\n        \"output\": \" No, BaBSbS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrBN2\\n\",\n        \"output\": \" No, PrBN2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2GaPd\\n\",\n        \"output\": \" Yes, Li2GaPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaCuTeO\\n\",\n        \"output\": \" No, LaCuTeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U2Cu2As3O\\n\",\n        \"output\": \" Yes, U2Cu2As3O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HfFe2\\n\",\n        \"output\": \" Yes, HfFe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.5In2.25Ag0.25Te4\\n\",\n        \"output\": \" No, Cd0.5In2.25Ag0.25Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2GaS4\\n\",\n        \"output\": \" No, Ba2GaS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2MoO5\\n\",\n        \"output\": \" No, La2MoO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SbPd3\\n\",\n        \"output\": \" Yes, SbPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YWO3\\n\",\n        \"output\": \" Yes, YWO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag8GeS6\\n\",\n        \"output\": \" No, Ag8GeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeSi2Ni\\n\",\n        \"output\": \" Yes, CeSi2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaSi2Pd3\\n\",\n        \"output\": \" Yes, NaSi2Pd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga2Si(AgS3)2\\n\",\n        \"output\": \" No, Ga2Si(AgS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgMnRh2\\n\",\n        \"output\": \" Yes, MgMnRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiB3O5\\n\",\n        \"output\": \" No, LiB3O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr1.33Ta0.67N2.61O0.42\\n\",\n        \"output\": \" No, Zr1.33Ta0.67N2.61O0.42 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlZn2Tc\\n\",\n        \"output\": \" Yes, TlZn2Tc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PbSe\\n\",\n        \"output\": \" No, PbSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn3(OF3)2\\n\",\n        \"output\": \" Yes, Mn3(OF3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Sb\\n\",\n        \"output\": \" No, Rb3Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Th6Mg23\\n\",\n        \"output\": \" Yes, Th6Mg23 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl3Pb\\n\",\n        \"output\": \" Yes, Tl3Pb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaTi4O8\\n\",\n        \"output\": \" Yes, CaTi4O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaCu3S4\\n\",\n        \"output\": \" No, TaCu3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VTe2\\n\",\n        \"output\": \" Yes, VTe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2GeS4\\n\",\n        \"output\": \" Yes, Mn2GeS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlSn\\n\",\n        \"output\": \" Yes, TlSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn1Se0.6S0.4\\n\",\n        \"output\": \" No, Sn1Se0.6S0.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd2Se3\\n\",\n        \"output\": \" No, Nd2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnO2\\n\",\n        \"output\": \" No, SnO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlCr5SeS7\\n\",\n        \"output\": \" No, TlCr5SeS7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(InAs)2\\n\",\n        \"output\": \" Yes, Eu(InAs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KTi2F7\\n\",\n        \"output\": \" No, KTi2F7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl2Te3As2Se\\n\",\n        \"output\": \" No, Tl2Te3As2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca(CoGe)2\\n\",\n        \"output\": \" Yes, Ca(CoGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr(InS2)3\\n\",\n        \"output\": \" No, Pr(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdHg6(As2Br3)2\\n\",\n        \"output\": \" No, CdHg6(As2Br3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" snail\\n\",\n        \"output\": \" snail is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" front\\n\",\n        \"output\": \" front is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu2Hg2SF6\\n\",\n        \"output\": \" Yes, Cu2Hg2SF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" DyZrSb\\n\",\n        \"output\": \" Yes, DyZrSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga2GePbSe6\\n\",\n        \"output\": \" No, Ga2GePbSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeB2Ir3\\n\",\n        \"output\": \" Yes, CeB2Ir3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(Ni2B)6\\n\",\n        \"output\": \" Yes, Eu(Ni2B)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeCoGeH\\n\",\n        \"output\": \" Yes, CeCoGeH is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho5Si4\\n\",\n        \"output\": \" Yes, Ho5Si4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba5(GaSe4)2\\n\",\n        \"output\": \" No, Ba5(GaSe4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3ZrRu2O9\\n\",\n        \"output\": \" Yes, Ba3ZrRu2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl2InGaTe4\\n\",\n        \"output\": \" No, Tl2InGaTe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NiI\\n\",\n        \"output\": \" Yes, NiI is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuCdAg2\\n\",\n        \"output\": \" Yes, LuCdAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.2Pb0.8Se1\\n\",\n        \"output\": \" No, Sn0.2Pb0.8Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Ga2Se5\\n\",\n        \"output\": \" No, Cs2Ga2Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmAs\\n\",\n        \"output\": \" No, TmAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu4Pd\\n\",\n        \"output\": \" Yes, Cu4Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Dy\\n\",\n        \"output\": \" Yes, Li3Dy is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsUCuS3\\n\",\n        \"output\": \" Yes, CsUCuS3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Hg3I8\\n\",\n        \"output\": \" No, Cs2Hg3I8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Re2RuBr\\n\",\n        \"output\": \" Yes, Re2RuBr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li6Tb2O7\\n\",\n        \"output\": \" Yes, Li6Tb2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.01Te0.01Pb0.99Se0.99\\n\",\n        \"output\": \" No, Ge0.01Te0.01Pb0.99Se0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnS\\n\",\n        \"output\": \" No, ZnS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AuBrO2\\n\",\n        \"output\": \" Yes, AuBrO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiBr2\\n\",\n        \"output\": \" Yes, TiBr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KSb5S8\\n\",\n        \"output\": \" No, KSb5S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3Ag\\n\",\n        \"output\": \" Yes, V3Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho2Co17\\n\",\n        \"output\": \" Yes, Ho2Co17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn2InCuSe4\\n\",\n        \"output\": \" No, Zn2InCuSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaGaAu3\\n\",\n        \"output\": \" Yes, CaGaAu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrTh(PS4)2\\n\",\n        \"output\": \" No, SrTh(PS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrRu3C\\n\",\n        \"output\": \" Yes, ZrRu3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdIn\\n\",\n        \"output\": \" No, CdIn is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.9Ga0.1As0.1P0.9\\n\",\n        \"output\": \" No, In0.9Ga0.1As0.1P0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrSi2\\n\",\n        \"output\": \" Yes, ZrSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbBr\\n\",\n        \"output\": \" No, RbBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn1Se0.99S0.01\\n\",\n        \"output\": \" No, Sn1Se0.99S0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" DyNiGe2\\n\",\n        \"output\": \" Yes, DyNiGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce3In3Ru2\\n\",\n        \"output\": \" Yes, Ce3In3Ru2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SiAs\\n\",\n        \"output\": \" No, SiAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PdO\\n\",\n        \"output\": \" No, PdO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiNb3(BiO3)4\\n\",\n        \"output\": \" No, LiNb3(BiO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy3GaS6\\n\",\n        \"output\": \" No, Dy3GaS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn2CoGe\\n\",\n        \"output\": \" Yes, Mn2CoGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbMoPO6\\n\",\n        \"output\": \" No, RbMoPO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb4Ag9(SbS3)4\\n\",\n        \"output\": \" No, Rb4Ag9(SbS3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb3Tm\\n\",\n        \"output\": \" Yes, Rb3Tm is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiIn2Rh\\n\",\n        \"output\": \" Yes, LiIn2Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2OsRu\\n\",\n        \"output\": \" Yes, Ti2OsRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4Ga4GeSe12\\n\",\n        \"output\": \" No, Ba4Ga4GeSe12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbZrPSe6\\n\",\n        \"output\": \" No, RbZrPSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2P\\n\",\n        \"output\": \" Yes, Mn2P is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgInAg2\\n\",\n        \"output\": \" Yes, MgInAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd2Ni7P4\\n\",\n        \"output\": \" Yes, Nd2Ni7P4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiTeI\\n\",\n        \"output\": \" No, BiTeI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.001Pb0.999Se1\\n\",\n        \"output\": \" No, Sn0.001Pb0.999Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Be3N2\\n\",\n        \"output\": \" No, Be3N2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr8Fe3N8\\n\",\n        \"output\": \" Yes, Sr8Fe3N8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlBiTe2\\n\",\n        \"output\": \" No, TlBiTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3CrO10\\n\",\n        \"output\": \" Yes, V3CrO10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnSiNi2\\n\",\n        \"output\": \" Yes, MnSiNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbCuSnSe3\\n\",\n        \"output\": \" No, RbCuSnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg3Al9FeSi5\\n\",\n        \"output\": \" Yes, Mg3Al9FeSi5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Cd3(B4O7)4\\n\",\n        \"output\": \" No, Cs2Cd3(B4O7)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HgBr2\\n\",\n        \"output\": \" No, HgBr2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2Be4B4O11\\n\",\n        \"output\": \" No, Na2Be4B4O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb3FeB7\\n\",\n        \"output\": \" Yes, Tb3FeB7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2Fe3CoO8\\n\",\n        \"output\": \" Yes, Li2Fe3CoO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YSn3\\n\",\n        \"output\": \" Yes, YSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaCdSi\\n\",\n        \"output\": \" Yes, CaCdSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4FeNi3O8\\n\",\n        \"output\": \" Yes, Li4FeNi3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr10Al4Si6O\\n\",\n        \"output\": \" Yes, Sr10Al4Si6O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb2C3\\n\",\n        \"output\": \" Yes, Tb2C3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbBi2\\n\",\n        \"output\": \" Yes, RbBi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErFeC2\\n\",\n        \"output\": \" Yes, ErFeC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd5Ge3\\n\",\n        \"output\": \" Yes, Nd5Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb6VSb3O25\\n\",\n        \"output\": \" No, Nb6VSb3O25 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd(InS2)2\\n\",\n        \"output\": \" No, Cd(InS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaHfZn\\n\",\n        \"output\": \" Yes, CaHfZn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2MnAlO5\\n\",\n        \"output\": \" Yes, Ca2MnAlO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaGa3Ni2\\n\",\n        \"output\": \" Yes, CaGa3Ni2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf3Sb\\n\",\n        \"output\": \" Yes, Hf3Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InSiTe3\\n\",\n        \"output\": \" Yes, InSiTe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuSb4Te7\\n\",\n        \"output\": \" No, EuSb4Te7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba6Ag2.7Sn4.3S16\\n\",\n        \"output\": \" No, Ba6Ag2.7Sn4.3S16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErAl9(Fe2Si3)2\\n\",\n        \"output\": \" Yes, ErAl9(Fe2Si3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyBPd3\\n\",\n        \"output\": \" Yes, DyBPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Sm2Ti3O10\\n\",\n        \"output\": \" No, K2Sm2Ti3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaCu6\\n\",\n        \"output\": \" Yes, LaCu6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg5Tl2\\n\",\n        \"output\": \" Yes, Mg5Tl2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mo3Pd2N\\n\",\n        \"output\": \" Yes, Mo3Pd2N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaSi2\\n\",\n        \"output\": \" No, BaSi2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi7O5F11\\n\",\n        \"output\": \" No, Bi7O5F11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Sn2Hg3S8\\n\",\n        \"output\": \" No, Rb2Sn2Hg3S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1.8Cu0.2Se2.8\\n\",\n        \"output\": \" No, In1.8Cu0.2Se2.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2Cd3Se4\\n\",\n        \"output\": \" No, Rb2Cd3Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(SbS2)2\\n\",\n        \"output\": \" No, Eu(SbS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na3WClO4\\n\",\n        \"output\": \" No, Na3WClO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiPb2S2I3\\n\",\n        \"output\": \" No, BiPb2S2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrInAu2\\n\",\n        \"output\": \" Yes, PrInAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc2S3\\n\",\n        \"output\": \" No, Sc2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScAg\\n\",\n        \"output\": \" Yes, ScAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg3P2\\n\",\n        \"output\": \" No, Mg3P2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.15Pb0.85Se1\\n\",\n        \"output\": \" No, Sn0.15Pb0.85Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd2Zn17\\n\",\n        \"output\": \" Yes, Gd2Zn17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr3NiO\\n\",\n        \"output\": \" Yes, Zr3NiO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsGaS3\\n\",\n        \"output\": \" No, CsGaS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlIr\\n\",\n        \"output\": \" Yes, AlIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CrFe2Sb\\n\",\n        \"output\": \" Yes, CrFe2Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaGeI\\n\",\n        \"output\": \" Yes, LaGeI is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2In5Au6\\n\",\n        \"output\": \" Yes, Na2In5Au6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdSb\\n\",\n        \"output\": \" No, CdSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GeI2\\n\",\n        \"output\": \" No, GeI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2Cd(GeS3)2\\n\",\n        \"output\": \" No, Na2Cd(GeS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" bankbook\\n\",\n        \"output\": \" bankbook is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2S2O\\n\",\n        \"output\": \" Yes, Ce2S2O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li(CuO)3\\n\",\n        \"output\": \" Yes, Li(CuO)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmCuSi\\n\",\n        \"output\": \" Yes, SmCuSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb17Ir3S40\\n\",\n        \"output\": \" Yes, Nb17Ir3S40 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga3SiAg3Se8\\n\",\n        \"output\": \" No, Ga3SiAg3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaLu(Pd3O4)2\\n\",\n        \"output\": \" Yes, NaLu(Pd3O4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaVO2\\n\",\n        \"output\": \" Yes, CaVO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3MgTa2O9\\n\",\n        \"output\": \" No, Ba3MgTa2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca(BC)2\\n\",\n        \"output\": \" Yes, Ca(BC)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmPbAu\\n\",\n        \"output\": \" Yes, SmPbAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PmSnRh2\\n\",\n        \"output\": \" Yes, PmSnRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YCdHg2\\n\",\n        \"output\": \" Yes, YCdHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn3(InS3)2\\n\",\n        \"output\": \" No, Zn3(InS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaHg2\\n\",\n        \"output\": \" Yes, CaHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr3P\\n\",\n        \"output\": \" Yes, Cr3P is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbCu2AsS3\\n\",\n        \"output\": \" No, RbCu2AsS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiAs2Os\\n\",\n        \"output\": \" Yes, BiAs2Os is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce4(GeS4)3\\n\",\n        \"output\": \" No, Ce4(GeS4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd(NiGe)2\\n\",\n        \"output\": \" Yes, Gd(NiGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KAg2\\n\",\n        \"output\": \" Yes, KAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KBiSe2\\n\",\n        \"output\": \" No, KBiSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbCuSnS3\\n\",\n        \"output\": \" No, RbCuSnS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy4Sb3\\n\",\n        \"output\": \" Yes, Dy4Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si3Ru2\\n\",\n        \"output\": \" No, Si3Ru2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd(SiRu)2\\n\",\n        \"output\": \" Yes, Gd(SiRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr(LaS2)2\\n\",\n        \"output\": \" No, Sr(LaS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4.5Ga0.5Te1O6\\n\",\n        \"output\": \" No, Li4.5Ga0.5Te1O6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2RbSb\\n\",\n        \"output\": \" No, K2RbSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Ta15O32\\n\",\n        \"output\": \" No, K2Ta15O32 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr2GaCo2O7\\n\",\n        \"output\": \" Yes, Sr2GaCo2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2GaSe4\\n\",\n        \"output\": \" No, Ba2GaSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaZn(MoO2)4\\n\",\n        \"output\": \" Yes, BaZn(MoO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" cup\\n\",\n        \"output\": \" cup is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te4Mo(WS)2\\n\",\n        \"output\": \" Yes, Te4Mo(WS)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaGaSe2\\n\",\n        \"output\": \" No, TaGaSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YCdPd2\\n\",\n        \"output\": \" Yes, YCdPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.85Hg0.15Se1\\n\",\n        \"output\": \" No, Zn0.85Hg0.15Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbCd4Ga5Te12\\n\",\n        \"output\": \" No, RbCd4Ga5Te12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb3Al3Ge7S20\\n\",\n        \"output\": \" No, Rb3Al3Ge7S20 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag(AuS)2\\n\",\n        \"output\": \" Yes, Ag(AuS)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Na(MoO4)2\\n\",\n        \"output\": \" No, Rb3Na(MoO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Cd3Te4\\n\",\n        \"output\": \" No, Rb2Cd3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ReIr3\\n\",\n        \"output\": \" Yes, ReIr3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn(FeN)2\\n\",\n        \"output\": \" Yes, Zn(FeN)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NiS2\\n\",\n        \"output\": \" No, NiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2TeI6\\n\",\n        \"output\": \" No, Rb2TeI6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Bi2Br9\\n\",\n        \"output\": \" No, Rb3Bi2Br9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.4Hg0.6Se1\\n\",\n        \"output\": \" No, Zn0.4Hg0.6Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb14Ti10O41\\n\",\n        \"output\": \" Yes, Yb14Ti10O41 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KUClO3\\n\",\n        \"output\": \" No, KUClO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UAl3\\n\",\n        \"output\": \" Yes, UAl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr(BRu)2\\n\",\n        \"output\": \" Yes, Pr(BRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn3NbO8\\n\",\n        \"output\": \" Yes, Mn3NbO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy3MnB7\\n\",\n        \"output\": \" Yes, Dy3MnB7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgMnO3\\n\",\n        \"output\": \" Yes, MgMnO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy4Te3S4\\n\",\n        \"output\": \" No, Dy4Te3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsYTe3O8\\n\",\n        \"output\": \" No, CsYTe3O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi1.4Sb0.6Te3\\n\",\n        \"output\": \" No, Bi1.4Sb0.6Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb(AlSi)2\\n\",\n        \"output\": \" Yes, Yb(AlSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.03Pb0.97Se1\\n\",\n        \"output\": \" No, Sn0.03Pb0.97Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiB9PbO15\\n\",\n        \"output\": \" No, LiB9PbO15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" back\\n\",\n        \"output\": \" back is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd4P2I3\\n\",\n        \"output\": \" No, Cd4P2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlCu3\\n\",\n        \"output\": \" Yes, AlCu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlCr5(SeS)4\\n\",\n        \"output\": \" No, TlCr5(SeS)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd3Bi(PO4)3\\n\",\n        \"output\": \" No, Cd3Bi(PO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KBiO3\\n\",\n        \"output\": \" Yes, KBiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" database\\n\",\n        \"output\": \" database is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdAs2\\n\",\n        \"output\": \" No, CdAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3Yb4O9\\n\",\n        \"output\": \" Yes, Ba3Yb4O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu3Bi6S10I\\n\",\n        \"output\": \" No, Cu3Bi6S10I is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2ZnSnSe4\\n\",\n        \"output\": \" No, Li2ZnSnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YMoClO4\\n\",\n        \"output\": \" No, YMoClO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2Cd2Te2O11\\n\",\n        \"output\": \" No, V2Cd2Te2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaTaNO2\\n\",\n        \"output\": \" No, CaTaNO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScTlS2\\n\",\n        \"output\": \" No, ScTlS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2TeSe3\\n\",\n        \"output\": \" No, Na2TeSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb2AgPS10\\n\",\n        \"output\": \" No, Nb2AgPS10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbPSe6\\n\",\n        \"output\": \" No, RbPSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InCuSe2\\n\",\n        \"output\": \" No, InCuSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K4Hf3Se14\\n\",\n        \"output\": \" No, K4Hf3Se14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy2MgIn\\n\",\n        \"output\": \" Yes, Dy2MgIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Gd3ReO7\\n\",\n        \"output\": \" Yes, Gd3ReO7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na11Bi5O16\\n\",\n        \"output\": \" Yes, Na11Bi5O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdH2NO5\\n\",\n        \"output\": \" No, GdH2NO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu2Se\\n\",\n        \"output\": \" No, Cu2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce3MoO7\\n\",\n        \"output\": \" No, Ce3MoO7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrB6\\n\",\n        \"output\": \" No, SrB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TiTe2\\n\",\n        \"output\": \" No, TiTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SnGeS3\\n\",\n        \"output\": \" No, SnGeS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.17Pb0.83Se1\\n\",\n        \"output\": \" No, Sn0.17Pb0.83Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb(GePd)2\\n\",\n        \"output\": \" Yes, Tb(GePd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbMn2O5\\n\",\n        \"output\": \" Yes, YbMn2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UAu2\\n\",\n        \"output\": \" Yes, UAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Tl\\n\",\n        \"output\": \" Yes, Na2Tl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu8O\\n\",\n        \"output\": \" Yes, Cu8O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg9CuO10\\n\",\n        \"output\": \" Yes, Mg9CuO10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho10Si17\\n\",\n        \"output\": \" Yes, Ho10Si17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3(AlGe)2\\n\",\n        \"output\": \" Yes, Ba3(AlGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlAgTe2\\n\",\n        \"output\": \" No, AlAgTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr5Al3\\n\",\n        \"output\": \" Yes, Zr5Al3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2Cu(NO)2\\n\",\n        \"output\": \" Yes, Ce2Cu(NO)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na3In2Au\\n\",\n        \"output\": \" Yes, Na3In2Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2(LuGe)3\\n\",\n        \"output\": \" Yes, Li2(LuGe)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y2C3\\n\",\n        \"output\": \" Yes, Y2C3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca4Al3O10\\n\",\n        \"output\": \" Yes, Ca4Al3O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba5Al2Ge7\\n\",\n        \"output\": \" Yes, Ba5Al2Ge7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" dragonfly\\n\",\n        \"output\": \" dragonfly is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb(CuSe)3\\n\",\n        \"output\": \" No, Yb(CuSe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na3Zn(BO2)5\\n\",\n        \"output\": \" No, Na3Zn(BO2)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaTiO3\\n\",\n        \"output\": \" No, BaTiO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiMnP2O7\\n\",\n        \"output\": \" Yes, LiMnP2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaEu2Mn2O7\\n\",\n        \"output\": \" Yes, BaEu2Mn2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiV2NiO6\\n\",\n        \"output\": \" Yes, LiV2NiO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbB5(H2O3)4\\n\",\n        \"output\": \" Yes, RbB5(H2O3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce3B2(ClO2)3\\n\",\n        \"output\": \" Yes, Ce3B2(ClO2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.01Sb0.99Te0.03\\n\",\n        \"output\": \" No, Ga1.01Sb0.99Te0.03 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2V9O13\\n\",\n        \"output\": \" Yes, Mg2V9O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PmMgCd2\\n\",\n        \"output\": \" Yes, PmMgCd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbB66\\n\",\n        \"output\": \" No, YbB66 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K(OsO3)2\\n\",\n        \"output\": \" Yes, K(OsO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs3Sb2I9\\n\",\n        \"output\": \" No, Cs3Sb2I9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrCd\\n\",\n        \"output\": \" Yes, ZrCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er4NiB13\\n\",\n        \"output\": \" Yes, Er4NiB13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La3CuGeSe7\\n\",\n        \"output\": \" No, La3CuGeSe7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2B4H2O9\\n\",\n        \"output\": \" No, Ba2B4H2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In11.3Bi14.7S38\\n\",\n        \"output\": \" No, In11.3Bi14.7S38 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Sb2I9\\n\",\n        \"output\": \" No, Rb3Sb2I9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga2HgS4\\n\",\n        \"output\": \" No, Ga2HgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdRh\\n\",\n        \"output\": \" Yes, NdRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlTe\\n\",\n        \"output\": \" Yes, TlTe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SnO\\n\",\n        \"output\": \" No, SnO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" IrSe2\\n\",\n        \"output\": \" No, IrSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" pvc\\n\",\n        \"output\": \" pvc is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2I4O13\\n\",\n        \"output\": \" No, Bi2I4O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La4Co3O10\\n\",\n        \"output\": \" Yes, La4Co3O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y2Fe2Si2C\\n\",\n        \"output\": \" Yes, Y2Fe2Si2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmC10\\n\",\n        \"output\": \" Yes, SmC10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaZnAsO\\n\",\n        \"output\": \" No, LaZnAsO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu3(BiI4)4\\n\",\n        \"output\": \" Yes, Cu3(BiI4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga2(TeO3)3\\n\",\n        \"output\": \" No, Ga2(TeO3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BPb7Br3O7\\n\",\n        \"output\": \" No, BPb7Br3O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Ti(CuS2)2\\n\",\n        \"output\": \" No, K2Ti(CuS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y(CuSi)2\\n\",\n        \"output\": \" Yes, Y(CuSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr7C3\\n\",\n        \"output\": \" Yes, Cr7C3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiSbS2\\n\",\n        \"output\": \" No, LiSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag2SnS3\\n\",\n        \"output\": \" No, Ag2SnS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KTa3(TeO6)2\\n\",\n        \"output\": \" No, KTa3(TeO6)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrZrS3\\n\",\n        \"output\": \" No, SrZrS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2Be17\\n\",\n        \"output\": \" Yes, Ti2Be17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaCdSb\\n\",\n        \"output\": \" Yes, NaCdSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba(SnO2)4\\n\",\n        \"output\": \" Yes, Ba(SnO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" P2Ir\\n\",\n        \"output\": \" No, P2Ir is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Hg3(GeS4)2\\n\",\n        \"output\": \" No, K2Hg3(GeS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3Cu\\n\",\n        \"output\": \" Yes, V3Cu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg3N2\\n\",\n        \"output\": \" No, Mg3N2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiBiS2\\n\",\n        \"output\": \" No, LiBiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaIn2Ir\\n\",\n        \"output\": \" Yes, BaIn2Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li15Mn2O12\\n\",\n        \"output\": \" Yes, Li15Mn2O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TaPd3\\n\",\n        \"output\": \" Yes, TaPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tc3Pd\\n\",\n        \"output\": \" Yes, Tc3Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U(CrC)4\\n\",\n        \"output\": \" Yes, U(CrC)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al5Rh2\\n\",\n        \"output\": \" Yes, Al5Rh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Cd(PSe3)2\\n\",\n        \"output\": \" No, K2Cd(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb2ZnPb\\n\",\n        \"output\": \" Yes, Yb2ZnPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Zn(SnSe3)2\\n\",\n        \"output\": \" No, K2Zn(SnSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu2Ga2GeS7\\n\",\n        \"output\": \" No, Eu2Ga2GeS7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti10O11\\n\",\n        \"output\": \" Yes, Ti10O11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmNiAs\\n\",\n        \"output\": \" Yes, SmNiAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiTlPd2\\n\",\n        \"output\": \" Yes, LiTlPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeAgSn\\n\",\n        \"output\": \" Yes, CeAgSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.8Ge0.2\\n\",\n        \"output\": \" No, Si0.8Ge0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NiAgO2\\n\",\n        \"output\": \" Yes, NiAgO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu3Hg2(Te3O8)2\\n\",\n        \"output\": \" No, Cu3Hg2(Te3O8)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrB2\\n\",\n        \"output\": \" Yes, ZrB2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce10Se14O\\n\",\n        \"output\": \" No, Ce10Se14O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2Cd(BO2)6\\n\",\n        \"output\": \" No, Ba2Cd(BO2)6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" FeAs2O7\\n\",\n        \"output\": \" Yes, FeAs2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.2Hg0.8Te1\\n\",\n        \"output\": \" No, Zn0.2Hg0.8Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2Se3\\n\",\n        \"output\": \" No, Ce2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2NbO6\\n\",\n        \"output\": \" Yes, K2NbO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu18S11\\n\",\n        \"output\": \" Yes, Cu18S11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb3Ru\\n\",\n        \"output\": \" Yes, Nb3Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaTi4O8\\n\",\n        \"output\": \" Yes, BaTi4O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgPb3\\n\",\n        \"output\": \" Yes, MgPb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce(CuSb)2\\n\",\n        \"output\": \" Yes, Ce(CuSb)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2ZnGe\\n\",\n        \"output\": \" No, Li2ZnGe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi8Te7S5\\n\",\n        \"output\": \" No, Bi8Te7S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" advertisement\\n\",\n        \"output\": \" advertisement is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsScBr3\\n\",\n        \"output\": \" Yes, CsScBr3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.7Hg0.3Se1\\n\",\n        \"output\": \" No, Cd0.7Hg0.3Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3Ti2(SiO4)3\\n\",\n        \"output\": \" No, Ca3Ti2(SiO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn(Bi19O29)2\\n\",\n        \"output\": \" No, Zn(Bi19O29)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd(Al4Co)2\\n\",\n        \"output\": \" Yes, Nd(Al4Co)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrUS2\\n\",\n        \"output\": \" Yes, SrUS2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsI\\n\",\n        \"output\": \" No, CsI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba12In4S19\\n\",\n        \"output\": \" No, Ba12In4S19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnNi\\n\",\n        \"output\": \" Yes, MnNi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm2Pd2Pb\\n\",\n        \"output\": \" Yes, Sm2Pd2Pb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn(SbSe2)2\\n\",\n        \"output\": \" No, Mn(SbSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag2Mo(I2O7)2\\n\",\n        \"output\": \" No, Ag2Mo(I2O7)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li4.5Al0.5Te1O6\\n\",\n        \"output\": \" No, Li4.5Al0.5Te1O6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThRh2\\n\",\n        \"output\": \" Yes, ThRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnGe\\n\",\n        \"output\": \" No, SnGe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GePbS3\\n\",\n        \"output\": \" No, GePbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SnRh\\n\",\n        \"output\": \" Yes, SnRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs4Ag9(SbS3)4\\n\",\n        \"output\": \" No, Cs4Ag9(SbS3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn11Si19\\n\",\n        \"output\": \" No, Mn11Si19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga0.001Te1Pb0.999\\n\",\n        \"output\": \" No, Ga0.001Te1Pb0.999 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y(CuSe)3\\n\",\n        \"output\": \" No, Y(CuSe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm2MgTl\\n\",\n        \"output\": \" Yes, Tm2MgTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Cl\\n\",\n        \"output\": \" Yes, Na2Cl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaBr\\n\",\n        \"output\": \" No, NaBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsLuCoS3\\n\",\n        \"output\": \" No, CsLuCoS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GdSe2\\n\",\n        \"output\": \" Yes, GdSe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlCr5(SeS3)2\\n\",\n        \"output\": \" No, TlCr5(SeS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Re(TeCl6)2\\n\",\n        \"output\": \" Yes, Re(TeCl6)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La16Mn15O48\\n\",\n        \"output\": \" Yes, La16Mn15O48 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiTiSiO4\\n\",\n        \"output\": \" Yes, LiTiSiO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm2CuTc\\n\",\n        \"output\": \" Yes, Tm2CuTc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si2SbO6\\n\",\n        \"output\": \" Yes, Si2SbO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga4SnSe7\\n\",\n        \"output\": \" No, Ga4SnSe7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeTaN2O\\n\",\n        \"output\": \" No, CeTaN2O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn5As4\\n\",\n        \"output\": \" Yes, Mn5As4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Mn4(PO4)6\\n\",\n        \"output\": \" Yes, Li3Mn4(PO4)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu0.96Bi2Se3I1\\n\",\n        \"output\": \" No, Cu0.96Bi2Se3I1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2Mo2O7\\n\",\n        \"output\": \" Yes, Sm2Mo2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbBiSe2\\n\",\n        \"output\": \" No, RbBiSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2V3FeO8\\n\",\n        \"output\": \" Yes, Li2V3FeO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pm2PtAu\\n\",\n        \"output\": \" Yes, Pm2PtAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pm2NiRh\\n\",\n        \"output\": \" Yes, Pm2NiRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y3Ge4\\n\",\n        \"output\": \" Yes, Y3Ge4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SiSe2\\n\",\n        \"output\": \" No, SiSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr6O\\n\",\n        \"output\": \" No, Zr6O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SiW3\\n\",\n        \"output\": \" Yes, SiW3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AsPPd\\n\",\n        \"output\": \" No, AsPPd is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaPb\\n\",\n        \"output\": \" Yes, CaPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrMgAg2\\n\",\n        \"output\": \" Yes, PrMgAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Te2SO10\\n\",\n        \"output\": \" No, Bi2Te2SO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiAsSe2\\n\",\n        \"output\": \" No, LiAsSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2ZrS5\\n\",\n        \"output\": \" No, La2ZrS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrSe\\n\",\n        \"output\": \" Yes, ZrSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm(NiSn)2\\n\",\n        \"output\": \" Yes, Sm(NiSn)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaP\\n\",\n        \"output\": \" No, GaP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NiTe\\n\",\n        \"output\": \" No, NiTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiCo(CO3)2\\n\",\n        \"output\": \" Yes, LiCo(CO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" certification\\n\",\n        \"output\": \" certification is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdCuSO\\n\",\n        \"output\": \" No, NdCuSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.95Cu0.05Se2.95\\n\",\n        \"output\": \" No, Ga1.95Cu0.05Se2.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(NdS2)2\\n\",\n        \"output\": \" No, Ca(NdS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.2Te1Pb0.8\\n\",\n        \"output\": \" No, Ge0.2Te1Pb0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.08Te0.08Pb0.92Se0.92\\n\",\n        \"output\": \" No, Sn0.08Te0.08Pb0.92Se0.92 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg(As2Rh3)2\\n\",\n        \"output\": \" Yes, Mg(As2Rh3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.9Hg0.1Te1\\n\",\n        \"output\": \" No, Zn0.9Hg0.1Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Si0.0645Ge0.9355\\n\",\n        \"output\": \" No, Si0.0645Ge0.9355 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" mascara\\n\",\n        \"output\": \" mascara is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaV\\n\",\n        \"output\": \" Yes, LaV is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag0.5Ge1Pb1.75Se4\\n\",\n        \"output\": \" No, Ag0.5Ge1Pb1.75Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuF3\\n\",\n        \"output\": \" Yes, EuF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb(Cl2O)2\\n\",\n        \"output\": \" Yes, Nb(Cl2O)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrAlPt\\n\",\n        \"output\": \" Yes, ZrAlPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag3AsSe3\\n\",\n        \"output\": \" No, Ag3AsSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdSnRh\\n\",\n        \"output\": \" Yes, NdSnRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsIr\\n\",\n        \"output\": \" Yes, CsIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La20Mo12Cl4O63\\n\",\n        \"output\": \" No, La20Mo12Cl4O63 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.4Ga0.6As1\\n\",\n        \"output\": \" No, In0.4Ga0.6As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi4Pb7Se13\\n\",\n        \"output\": \" No, Bi4Pb7Se13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" USbSe\\n\",\n        \"output\": \" Yes, USbSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi1.8Sb0.2Te3\\n\",\n        \"output\": \" No, Bi1.8Sb0.2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Co4TeO8\\n\",\n        \"output\": \" Yes, Li3Co4TeO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(AlZn)2\\n\",\n        \"output\": \" Yes, Ca(AlZn)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ReBiO3\\n\",\n        \"output\": \" Yes, ReBiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ir0.67S2\\n\",\n        \"output\": \" No, Ir0.67S2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd2InAgTe3\\n\",\n        \"output\": \" No, Cd2InAgTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnGeRh2\\n\",\n        \"output\": \" Yes, MnGeRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaZn2\\n\",\n        \"output\": \" Yes, CaZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti11O18\\n\",\n        \"output\": \" Yes, Ti11O18 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr3Co2S2O5\\n\",\n        \"output\": \" Yes, Sr3Co2S2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" As2Pt\\n\",\n        \"output\": \" No, As2Pt is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Co3H\\n\",\n        \"output\": \" Yes, Co3H is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AsPRu\\n\",\n        \"output\": \" No, AsPRu is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" VAg(PSe3)2\\n\",\n        \"output\": \" Yes, VAg(PSe3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlSb\\n\",\n        \"output\": \" No, AlSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.6Ga0.4As0.4Se0.6\\n\",\n        \"output\": \" No, Zn0.6Ga0.4As0.4Se0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdAl4Ge2Au\\n\",\n        \"output\": \" Yes, NdAl4Ge2Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuPd\\n\",\n        \"output\": \" Yes, CuPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgV4O6\\n\",\n        \"output\": \" Yes, MgV4O6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnSb3(PO4)6\\n\",\n        \"output\": \" Yes, MnSb3(PO4)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La3ZrSb5\\n\",\n        \"output\": \" Yes, La3ZrSb5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" bengal\\n\",\n        \"output\": \" bengal is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti20(Sb3Se)3\\n\",\n        \"output\": \" Yes, Ti20(Sb3Se)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" H7Se2NO6\\n\",\n        \"output\": \" No, H7Se2NO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RhS3\\n\",\n        \"output\": \" No, RhS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsIrO3\\n\",\n        \"output\": \" Yes, CsIrO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrCuBi\\n\",\n        \"output\": \" Yes, SrCuBi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Nb2CoO9\\n\",\n        \"output\": \" Yes, Ba3Nb2CoO9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3(BN2)2\\n\",\n        \"output\": \" No, Ca3(BN2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb4CuSi2O7\\n\",\n        \"output\": \" Yes, Rb4CuSi2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiGaS2\\n\",\n        \"output\": \" No, LiGaS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuSnO3\\n\",\n        \"output\": \" Yes, EuSnO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2CrCuO4\\n\",\n        \"output\": \" Yes, Li2CrCuO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf(VGa2)2\\n\",\n        \"output\": \" Yes, Hf(VGa2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiAl2Tc\\n\",\n        \"output\": \" Yes, LiAl2Tc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuSbO3\\n\",\n        \"output\": \" Yes, EuSbO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PtN\\n\",\n        \"output\": \" Yes, PtN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd3Co11B4\\n\",\n        \"output\": \" Yes, Gd3Co11B4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy3Ga\\n\",\n        \"output\": \" Yes, Dy3Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr4Te3(ClO2)4\\n\",\n        \"output\": \" No, Sr4Te3(ClO2)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd2InCuTe3\\n\",\n        \"output\": \" No, Cd2InCuTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsYZnSe3\\n\",\n        \"output\": \" No, CsYZnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2Bi4O11\\n\",\n        \"output\": \" No, V2Bi4O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.99Te1Pb0.01\\n\",\n        \"output\": \" No, Sn0.99Te1Pb0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnSb\\n\",\n        \"output\": \" No, ZnSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KTm\\n\",\n        \"output\": \" Yes, KTm is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaSc(SeO3)2\\n\",\n        \"output\": \" No, NaSc(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaAl2\\n\",\n        \"output\": \" Yes, BaAl2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl0.001Te1Pb0.999\\n\",\n        \"output\": \" No, Tl0.001Te1Pb0.999 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaPd(IO3)4\\n\",\n        \"output\": \" No, BaPd(IO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BP\\n\",\n        \"output\": \" No, BP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2ErGaSe5\\n\",\n        \"output\": \" No, Ba2ErGaSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KRbBi8Se13\\n\",\n        \"output\": \" No, KRbBi8Se13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" sun\\n\",\n        \"output\": \" sun is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NbRu2Cl\\n\",\n        \"output\": \" Yes, NbRu2Cl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho2Ge5Rh3\\n\",\n        \"output\": \" Yes, Ho2Ge5Rh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn(InSe2)2\\n\",\n        \"output\": \" No, Zn(InSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta4AlC3\\n\",\n        \"output\": \" Yes, Ta4AlC3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2SiB4O9\\n\",\n        \"output\": \" No, Cs2SiB4O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb9Bi13S24\\n\",\n        \"output\": \" No, Rb9Bi13S24 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiHgO3\\n\",\n        \"output\": \" Yes, TiHgO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SnCl2\\n\",\n        \"output\": \" No, SnCl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2ZrSe5\\n\",\n        \"output\": \" No, Sm2ZrSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScSi3Ni\\n\",\n        \"output\": \" Yes, ScSi3Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Te\\n\",\n        \"output\": \" Yes, Ba3Te is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb3(MnC3)2\\n\",\n        \"output\": \" Yes, Tb3(MnC3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La5Cu6.33S7O4\\n\",\n        \"output\": \" No, La5Cu6.33S7O4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmU2S3O2\\n\",\n        \"output\": \" Yes, TmU2S3O2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuP2\\n\",\n        \"output\": \" No, CuP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2MgHg\\n\",\n        \"output\": \" Yes, Li2MgHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4Mn5NbO12\\n\",\n        \"output\": \" Yes, Li4Mn5NbO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn3Ir2Se3\\n\",\n        \"output\": \" No, Sn3Ir2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.15Ga0.85As1\\n\",\n        \"output\": \" No, Al0.15Ga0.85As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HfNi5\\n\",\n        \"output\": \" Yes, HfNi5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Er6MnBi2\\n\",\n        \"output\": \" Yes, Er6MnBi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm(BOs)2\\n\",\n        \"output\": \" Yes, Sm(BOs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba(BO2)2\\n\",\n        \"output\": \" No, Ba(BO2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd(NiSn)2\\n\",\n        \"output\": \" Yes, Nd(NiSn)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyMn2\\n\",\n        \"output\": \" Yes, DyMn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb4GaSbS9\\n\",\n        \"output\": \" No, Tb4GaSbS9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiBrO\\n\",\n        \"output\": \" No, BiBrO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeMg2Ag\\n\",\n        \"output\": \" Yes, CeMg2Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2Yb(CuO2)4\\n\",\n        \"output\": \" Yes, Ba2Yb(CuO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" InAgO2\\n\",\n        \"output\": \" No, InAgO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KNbSe2O7\\n\",\n        \"output\": \" No, KNbSe2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdSnP2\\n\",\n        \"output\": \" No, CdSnP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho(SbO3)2\\n\",\n        \"output\": \" Yes, Ho(SbO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VO2\\n\",\n        \"output\": \" No, VO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr2InPd2\\n\",\n        \"output\": \" Yes, Pr2InPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2Cu2Sb2S5\\n\",\n        \"output\": \" No, Cs2Cu2Sb2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiYbF4\\n\",\n        \"output\": \" Yes, LiYbF4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe2S\\n\",\n        \"output\": \" Yes, Fe2S is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La10Se14O\\n\",\n        \"output\": \" No, La10Se14O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KSb(SO4)2\\n\",\n        \"output\": \" No, KSb(SO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2CuO4\\n\",\n        \"output\": \" Yes, La2CuO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd2AgRh\\n\",\n        \"output\": \" Yes, Cd2AgRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiBr3\\n\",\n        \"output\": \" No, BiBr3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi9S6O7.5\\n\",\n        \"output\": \" No, Bi9S6O7.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr(BiO3)2\\n\",\n        \"output\": \" Yes, Pr(BiO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PrMgGa\\n\",\n        \"output\": \" Yes, PrMgGa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" himalayan\\n\",\n        \"output\": \" himalayan is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K10Sn3(PSe3)8\\n\",\n        \"output\": \" No, K10Sn3(PSe3)8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb28(Mg3In17)3\\n\",\n        \"output\": \" Yes, Rb28(Mg3In17)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li6FeO5F\\n\",\n        \"output\": \" Yes, Li6FeO5F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GeTe2\\n\",\n        \"output\": \" No, GeTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy2O3\\n\",\n        \"output\": \" No, Dy2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaRe2Ag\\n\",\n        \"output\": \" Yes, LaRe2Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2RuCl6\\n\",\n        \"output\": \" Yes, K2RuCl6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2DyCu3Te4\\n\",\n        \"output\": \" No, Cs2DyCu3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiMn2Al\\n\",\n        \"output\": \" Yes, TiMn2Al is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsInTe3O8\\n\",\n        \"output\": \" No, CsInTe3O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge0.39Te1Pb0.61\\n\",\n        \"output\": \" No, Ge0.39Te1Pb0.61 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr5SiSb3\\n\",\n        \"output\": \" Yes, Zr5SiSb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Sn2Hg3S8\\n\",\n        \"output\": \" No, K2Sn2Hg3S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y(SiRh)2\\n\",\n        \"output\": \" Yes, Y(SiRh)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbP\\n\",\n        \"output\": \" Yes, TbP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlCr5Se5S3\\n\",\n        \"output\": \" No, TlCr5Se5S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2SCl6F\\n\",\n        \"output\": \" Yes, Rb2SCl6F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3ScN2\\n\",\n        \"output\": \" No, Li3ScN2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl0.005Te1Pb0.995\\n\",\n        \"output\": \" No, Tl0.005Te1Pb0.995 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ICl2\\n\",\n        \"output\": \" Yes, ICl2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na0.5Ge1Pb1.75Se4\\n\",\n        \"output\": \" No, Na0.5Ge1Pb1.75Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La3AlN\\n\",\n        \"output\": \" Yes, La3AlN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd2ZrS5\\n\",\n        \"output\": \" No, Gd2ZrS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2SmTaO6\\n\",\n        \"output\": \" No, Ba2SmTaO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb(SbS2)2\\n\",\n        \"output\": \" No, Yb(SbS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1.01Cu0.99Se2.01\\n\",\n        \"output\": \" No, In1.01Cu0.99Se2.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al6Fe\\n\",\n        \"output\": \" Yes, Al6Fe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsNbSe2O7\\n\",\n        \"output\": \" No, CsNbSe2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfSe2\\n\",\n        \"output\": \" No, HfSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiAsRh\\n\",\n        \"output\": \" Yes, TiAsRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2V6O13\\n\",\n        \"output\": \" Yes, Na2V6O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2MnCu3O8\\n\",\n        \"output\": \" Yes, Li2MnCu3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb3Sn13Rh4\\n\",\n        \"output\": \" Yes, Yb3Sn13Rh4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu3Se4\\n\",\n        \"output\": \" No, Eu3Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" transmission\\n\",\n        \"output\": \" transmission is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuSeClO3\\n\",\n        \"output\": \" Yes, EuSeClO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsSc(SeO3)2\\n\",\n        \"output\": \" No, CsSc(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" WO3\\n\",\n        \"output\": \" No, WO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr(CoAs)2\\n\",\n        \"output\": \" Yes, Pr(CoAs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2YReO6\\n\",\n        \"output\": \" Yes, Ba2YReO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YMgCu4\\n\",\n        \"output\": \" Yes, YMgCu4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2Te3\\n\",\n        \"output\": \" No, Sm2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaAsS2\\n\",\n        \"output\": \" No, NaAsS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InPt\\n\",\n        \"output\": \" Yes, InPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.99Ga0.01As0.01Se0.99\\n\",\n        \"output\": \" No, Zn0.99Ga0.01As0.01Se0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd1.33Lu0.67S3\\n\",\n        \"output\": \" No, Nd1.33Lu0.67S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" pastor\\n\",\n        \"output\": \" pastor is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaIn2(P2O7)2\\n\",\n        \"output\": \" No, BaIn2(P2O7)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2Zn(GeS3)2\\n\",\n        \"output\": \" No, Na2Zn(GeS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VSb\\n\",\n        \"output\": \" Yes, VSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" As2Ir\\n\",\n        \"output\": \" No, As2Ir is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al4Cu9\\n\",\n        \"output\": \" Yes, Al4Cu9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca5Sn4S13\\n\",\n        \"output\": \" Yes, Ca5Sn4S13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Th3B2C3\\n\",\n        \"output\": \" Yes, Th3B2C3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.1Cu0.9Se2.1\\n\",\n        \"output\": \" No, Ga1.1Cu0.9Se2.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2Fe17\\n\",\n        \"output\": \" Yes, Ce2Fe17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiI3\\n\",\n        \"output\": \" No, BiI3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrTlSe2\\n\",\n        \"output\": \" No, PrTlSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VPt2\\n\",\n        \"output\": \" Yes, VPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.9Ga0.1P0.1S0.9\\n\",\n        \"output\": \" No, Zn0.9Ga0.1P0.1S0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ni2Te3O8\\n\",\n        \"output\": \" No, Ni2Te3O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2V2IO9\\n\",\n        \"output\": \" No, La2V2IO9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.4Ga0.6P1\\n\",\n        \"output\": \" No, In0.4Ga0.6P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca2Ti9O13\\n\",\n        \"output\": \" Yes, Ca2Ti9O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FeCoAs\\n\",\n        \"output\": \" Yes, FeCoAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Fe2SbO6\\n\",\n        \"output\": \" Yes, Li3Fe2SbO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca2TlCd\\n\",\n        \"output\": \" Yes, Ca2TlCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2Zn(SeO)2\\n\",\n        \"output\": \" No, La2Zn(SeO)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YMoO4F\\n\",\n        \"output\": \" No, YMoO4F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbNd3\\n\",\n        \"output\": \" Yes, YbNd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdSbPd\\n\",\n        \"output\": \" Yes, NdSbPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb3Sm\\n\",\n        \"output\": \" Yes, Rb3Sm is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm1.82Lu2.18Se6\\n\",\n        \"output\": \" No, Sm1.82Lu2.18Se6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2YBi2O7\\n\",\n        \"output\": \" Yes, Sr2YBi2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" VBi(SeO4)2\\n\",\n        \"output\": \" No, VBi(SeO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ReSi2\\n\",\n        \"output\": \" No, ReSi2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScCdAg2\\n\",\n        \"output\": \" Yes, ScCdAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" steam\\n\",\n        \"output\": \" steam is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FePS\\n\",\n        \"output\": \" No, FePS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaCeS2\\n\",\n        \"output\": \" Yes, NaCeS2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(POs)2\\n\",\n        \"output\": \" Yes, Eu(POs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn5O7\\n\",\n        \"output\": \" Yes, Mn5O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnAl3\\n\",\n        \"output\": \" No, MnAl3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb(InS2)3\\n\",\n        \"output\": \" No, Tb(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1Sb0.9As0.1\\n\",\n        \"output\": \" No, In1Sb0.9As0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaS\\n\",\n        \"output\": \" No, GaS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2In2GeSe6\\n\",\n        \"output\": \" No, Li2In2GeSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaAs\\n\",\n        \"output\": \" Yes, TaAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Th(CuS2)2\\n\",\n        \"output\": \" No, K2Th(CuS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2ScSbO6\\n\",\n        \"output\": \" No, Ca2ScSbO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y3Tm\\n\",\n        \"output\": \" Yes, Y3Tm is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrS2\\n\",\n        \"output\": \" No, ZrS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2PdSe10\\n\",\n        \"output\": \" No, K2PdSe10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag7AsSe6\\n\",\n        \"output\": \" No, Ag7AsSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlCuSe2\\n\",\n        \"output\": \" No, TlCuSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2Sn5\\n\",\n        \"output\": \" Yes, Li2Sn5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaPt5\\n\",\n        \"output\": \" Yes, LaPt5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" No, Ag0.5Ge1Pb1.75S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Lu2O3\\n\",\n        \"output\": \" No, Lu2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdSnO3\\n\",\n        \"output\": \" No, CdSnO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs5Mo21Se23\\n\",\n        \"output\": \" Yes, Cs5Mo21Se23 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuAgSb\\n\",\n        \"output\": \" Yes, EuAgSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmHoZn2\\n\",\n        \"output\": \" Yes, SmHoZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te2Pd3\\n\",\n        \"output\": \" Yes, Te2Pd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" B6As\\n\",\n        \"output\": \" No, B6As is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaNb4O6\\n\",\n        \"output\": \" Yes, BaNb4O6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" makeup\\n\",\n        \"output\": \" makeup is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" gear\\n\",\n        \"output\": \" gear is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In(PS2)2\\n\",\n        \"output\": \" No, In(PS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScBPd3\\n\",\n        \"output\": \" Yes, ScBPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2CeInTe5\\n\",\n        \"output\": \" No, Ba2CeInTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsGe5BO12\\n\",\n        \"output\": \" No, CsGe5BO12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbNa2NiO2\\n\",\n        \"output\": \" Yes, RbNa2NiO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho5(Ge5Rh2)2\\n\",\n        \"output\": \" Yes, Ho5(Ge5Rh2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho2CuRh\\n\",\n        \"output\": \" Yes, Ho2CuRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AlP\\n\",\n        \"output\": \" No, AlP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KYb2F7\\n\",\n        \"output\": \" Yes, KYb2F7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnI2\\n\",\n        \"output\": \" No, SnI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaAgSe2\\n\",\n        \"output\": \" No, GaAgSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl2TeS3\\n\",\n        \"output\": \" No, Tl2TeS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnTe\\n\",\n        \"output\": \" No, SnTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb2(MoO4)3\\n\",\n        \"output\": \" No, Tb2(MoO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" B2Mo(PbO2)6\\n\",\n        \"output\": \" No, B2Mo(PbO2)6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2VCuF7\\n\",\n        \"output\": \" Yes, Na2VCuF7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiCoSn\\n\",\n        \"output\": \" Yes, TiCoSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce3NbS3O4\\n\",\n        \"output\": \" Yes, Ce3NbS3O4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2YGaTe5\\n\",\n        \"output\": \" No, Ba2YGaTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Be12Pt\\n\",\n        \"output\": \" Yes, Be12Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Ba3(P2O7)2\\n\",\n        \"output\": \" No, Cs2Ba3(P2O7)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuGe2\\n\",\n        \"output\": \" Yes, LuGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgSnRh2\\n\",\n        \"output\": \" Yes, MgSnRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeP\\n\",\n        \"output\": \" Yes, FeP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti3Fe3O\\n\",\n        \"output\": \" Yes, Ti3Fe3O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na3Re\\n\",\n        \"output\": \" Yes, Na3Re is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PdSe2\\n\",\n        \"output\": \" No, PdSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.99In0.01P1\\n\",\n        \"output\": \" No, Al0.99In0.01P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr3Hg\\n\",\n        \"output\": \" Yes, Zr3Hg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na5Cu7O13\\n\",\n        \"output\": \" Yes, Na5Cu7O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Mo2Se2O11\\n\",\n        \"output\": \" No, K2Mo2Se2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" helicopter\\n\",\n        \"output\": \" helicopter is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsSbSe2\\n\",\n        \"output\": \" No, CsSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er2Te3\\n\",\n        \"output\": \" No, Er2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaH2NO5\\n\",\n        \"output\": \" No, LaH2NO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2.15Sb8.15Pb1.7Se15\\n\",\n        \"output\": \" No, K2.15Sb8.15Pb1.7Se15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgCuBi\\n\",\n        \"output\": \" Yes, MgCuBi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" sock\\n\",\n        \"output\": \" sock is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2CaReO6\\n\",\n        \"output\": \" Yes, Ba2CaReO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuPtO2\\n\",\n        \"output\": \" Yes, CuPtO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu15Si4\\n\",\n        \"output\": \" Yes, Cu15Si4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2O3\\n\",\n        \"output\": \" No, Tl2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3CrCo3O8\\n\",\n        \"output\": \" Yes, Li3CrCo3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CoPbO3\\n\",\n        \"output\": \" Yes, CoPbO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2GeB2Rh5\\n\",\n        \"output\": \" Yes, Mg2GeB2Rh5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce4InSbSe9\\n\",\n        \"output\": \" No, Ce4InSbSe9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiErAu2\\n\",\n        \"output\": \" Yes, LiErAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr3Al2\\n\",\n        \"output\": \" Yes, Zr3Al2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te3MoWS\\n\",\n        \"output\": \" Yes, Te3MoWS is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti13S24\\n\",\n        \"output\": \" Yes, Ti13S24 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Ni3TeO8\\n\",\n        \"output\": \" Yes, Li2Ni3TeO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La5In3(S3O)3\\n\",\n        \"output\": \" No, La5In3(S3O)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na3(WO3)4\\n\",\n        \"output\": \" Yes, Na3(WO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Er2Se3\\n\",\n        \"output\": \" No, Er2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaPrO3\\n\",\n        \"output\": \" No, BaPrO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta2O5\\n\",\n        \"output\": \" No, Ta2O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2Ga2GeS6\\n\",\n        \"output\": \" No, Na2Ga2GeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2Se\\n\",\n        \"output\": \" No, Tl2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmSnPd\\n\",\n        \"output\": \" Yes, SmSnPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YCd4B3O10\\n\",\n        \"output\": \" No, YCd4B3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Zn(GeSe3)2\\n\",\n        \"output\": \" No, Na2Zn(GeSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(MgBi)2\\n\",\n        \"output\": \" Yes, Eu(MgBi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnGeP2\\n\",\n        \"output\": \" No, ZnGeP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HgTeBr\\n\",\n        \"output\": \" No, HgTeBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" appliance\\n\",\n        \"output\": \" appliance is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na8PO3\\n\",\n        \"output\": \" Yes, Na8PO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2MnO2F\\n\",\n        \"output\": \" Yes, Li2MnO2F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaAsSe2\\n\",\n        \"output\": \" No, NaAsSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1.3Cu0.7Se2.3\\n\",\n        \"output\": \" No, In1.3Cu0.7Se2.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HfB\\n\",\n        \"output\": \" Yes, HfB is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Th(MnGe)2\\n\",\n        \"output\": \" Yes, Th(MnGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KV2I3O13\\n\",\n        \"output\": \" No, KV2I3O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaHgSe2\\n\",\n        \"output\": \" No, BaHgSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.1Pb0.9Se1\\n\",\n        \"output\": \" No, Ge0.1Pb0.9Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1Sb0.4As0.6\\n\",\n        \"output\": \" No, In1Sb0.4As0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdO\\n\",\n        \"output\": \" No, CdO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag8SnSe6\\n\",\n        \"output\": \" No, Ag8SnSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2Fe(SeO)2\\n\",\n        \"output\": \" No, La2Fe(SeO)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu1.75Ag0.5Ge1S4\\n\",\n        \"output\": \" No, Eu1.75Ag0.5Ge1S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaBPt3\\n\",\n        \"output\": \" Yes, LaBPt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3NiBr3\\n\",\n        \"output\": \" Yes, La3NiBr3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NbSiIr\\n\",\n        \"output\": \" Yes, NbSiIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiTlS2\\n\",\n        \"output\": \" No, TiTlS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnBr2\\n\",\n        \"output\": \" No, SnBr2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti3Be\\n\",\n        \"output\": \" Yes, Ti3Be is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlFe4(CuO4)3\\n\",\n        \"output\": \" Yes, AlFe4(CuO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu2O3\\n\",\n        \"output\": \" No, Eu2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd2Se3\\n\",\n        \"output\": \" No, Gd2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn(CoO2)4\\n\",\n        \"output\": \" Yes, Mn(CoO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.2Pb0.8Se1\\n\",\n        \"output\": \" No, Ge0.2Pb0.8Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaNi2O3\\n\",\n        \"output\": \" Yes, NaNi2O3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn0.06Pb0.94Se1\\n\",\n        \"output\": \" No, Sn0.06Pb0.94Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2S3\\n\",\n        \"output\": \" No, Ce2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag3Pd\\n\",\n        \"output\": \" Yes, Ag3Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3NaIrO6\\n\",\n        \"output\": \" Yes, Ba3NaIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb8Ge3Sb5\\n\",\n        \"output\": \" Yes, Yb8Ge3Sb5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaTi4O7\\n\",\n        \"output\": \" Yes, BaTi4O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2Ge5Rh3\\n\",\n        \"output\": \" Yes, La2Ge5Rh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pb1Se0.01S0.99\\n\",\n        \"output\": \" No, Pb1Se0.01S0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2(SbPd3)3\\n\",\n        \"output\": \" Yes, Ce2(SbPd3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu1.83Ta15O32\\n\",\n        \"output\": \" No, Eu1.83Ta15O32 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PbN6\\n\",\n        \"output\": \" No, PbN6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm(CuS)3\\n\",\n        \"output\": \" No, Sm(CuS)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2O5\\n\",\n        \"output\": \" Yes, Bi2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li7Ti5O12\\n\",\n        \"output\": \" Yes, Li7Ti5O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu(FeSi)2\\n\",\n        \"output\": \" Yes, Eu(FeSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb(CoB)2\\n\",\n        \"output\": \" Yes, Tb(CoB)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiEr2Ga\\n\",\n        \"output\": \" Yes, LiEr2Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbS\\n\",\n        \"output\": \" No, YbS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn2AlO4\\n\",\n        \"output\": \" Yes, Mn2AlO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd2(MoO4)3\\n\",\n        \"output\": \" No, Gd2(MoO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlAgSe2\\n\",\n        \"output\": \" No, AlAgSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Lu2Al3Co\\n\",\n        \"output\": \" Yes, Lu2Al3Co is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScSbRu2\\n\",\n        \"output\": \" Yes, ScSbRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" dinosaur\\n\",\n        \"output\": \" dinosaur is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na4Mg(GeSe3)2\\n\",\n        \"output\": \" No, Na4Mg(GeSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeSbO3\\n\",\n        \"output\": \" Yes, CeSbO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te0.5Pb1Se0.5\\n\",\n        \"output\": \" No, Te0.5Pb1Se0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgCu2SiS4\\n\",\n        \"output\": \" No, MgCu2SiS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SnPt3C\\n\",\n        \"output\": \" Yes, SnPt3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuIr2\\n\",\n        \"output\": \" Yes, LuIr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnV(TeO4)2\\n\",\n        \"output\": \" No, MnV(TeO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.01Hg0.99Se1\\n\",\n        \"output\": \" No, Cd0.01Hg0.99Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(LaS2)2\\n\",\n        \"output\": \" No, Ca(LaS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2Ga\\n\",\n        \"output\": \" Yes, Li2Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbNbSe2O7\\n\",\n        \"output\": \" No, RbNbSe2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbSeBr\\n\",\n        \"output\": \" No, SbSeBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd(CuTe)3\\n\",\n        \"output\": \" No, Gd(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" drive\\n\",\n        \"output\": \" drive is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2SnSe4\\n\",\n        \"output\": \" No, Ba2SnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc3GaC\\n\",\n        \"output\": \" Yes, Sc3GaC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2Ga2GeS6\\n\",\n        \"output\": \" No, Li2Ga2GeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErCu\\n\",\n        \"output\": \" Yes, ErCu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al21Pt8\\n\",\n        \"output\": \" Yes, Al21Pt8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbPt\\n\",\n        \"output\": \" Yes, TbPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HoGeAu\\n\",\n        \"output\": \" Yes, HoGeAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2Cd3S4\\n\",\n        \"output\": \" No, Rb2Cd3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Sn(AuS2)2\\n\",\n        \"output\": \" No, K2Sn(AuS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" fly\\n\",\n        \"output\": \" fly is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" W2C\\n\",\n        \"output\": \" Yes, W2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrSe2\\n\",\n        \"output\": \" No, ZrSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdSiAs2\\n\",\n        \"output\": \" No, CdSiAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnTc\\n\",\n        \"output\": \" No, ZnTc is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmCo2\\n\",\n        \"output\": \" Yes, SmCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaCu2SnSe4\\n\",\n        \"output\": \" No, BaCu2SnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiMnSiO4\\n\",\n        \"output\": \" Yes, LiMnSiO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu(GaTe2)2\\n\",\n        \"output\": \" No, Eu(GaTe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlCr5S8\\n\",\n        \"output\": \" No, TlCr5S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YN\\n\",\n        \"output\": \" No, YN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YCuO2\\n\",\n        \"output\": \" No, YCuO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(SbSe2)2\\n\",\n        \"output\": \" No, Eu(SbSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2AlB2\\n\",\n        \"output\": \" Yes, Mn2AlB2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.2Ga0.8Sb0.8Te0.2\\n\",\n        \"output\": \" No, Cd0.2Ga0.8Sb0.8Te0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.1Hg0.9Se1\\n\",\n        \"output\": \" No, Cd0.1Hg0.9Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd1Hg6.5As4Cl6\\n\",\n        \"output\": \" No, Cd1Hg6.5As4Cl6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3(BN2)2\\n\",\n        \"output\": \" Yes, La3(BN2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2Fe2I\\n\",\n        \"output\": \" Yes, La2Fe2I is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga2SnGeS6\\n\",\n        \"output\": \" No, Ga2SnGeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiMnO2\\n\",\n        \"output\": \" Yes, LiMnO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2Hg3S4\\n\",\n        \"output\": \" No, Cs2Hg3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb5Ti5O17\\n\",\n        \"output\": \" Yes, Tb5Ti5O17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyZnRh2\\n\",\n        \"output\": \" Yes, DyZnRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.75Cd0.25Se1\\n\",\n        \"output\": \" No, Zn0.75Cd0.25Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" diving\\n\",\n        \"output\": \" diving is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" result\\n\",\n        \"output\": \" result is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrHCl\\n\",\n        \"output\": \" Yes, ZrHCl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Mo3Se3O16\\n\",\n        \"output\": \" No, Rb2Mo3Se3O16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce4Si3Rh4\\n\",\n        \"output\": \" Yes, Ce4Si3Rh4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2In2S5\\n\",\n        \"output\": \" No, Ba2In2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba6Sn6Se13\\n\",\n        \"output\": \" No, Ba6Sn6Se13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrGe2\\n\",\n        \"output\": \" No, SrGe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuAl2O4\\n\",\n        \"output\": \" No, EuAl2O4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbTa3(TeO6)2\\n\",\n        \"output\": \" No, RbTa3(TeO6)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.1Pb0.9Se1\\n\",\n        \"output\": \" No, Sn0.1Pb0.9Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu7(Ga3Sb4)2\\n\",\n        \"output\": \" No, Eu7(Ga3Sb4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbCd(BO2)3\\n\",\n        \"output\": \" No, RbCd(BO2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CuPO4F\\n\",\n        \"output\": \" Yes, CuPO4F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce3(Al3Ru)4\\n\",\n        \"output\": \" Yes, Ce3(Al3Ru)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" FeAg3(CN)6\\n\",\n        \"output\": \" Yes, FeAg3(CN)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaSbSe2\\n\",\n        \"output\": \" No, NaSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2NaMnF6\\n\",\n        \"output\": \" Yes, Cs2NaMnF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsRbP\\n\",\n        \"output\": \" Yes, CsRbP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi3BTeO9\\n\",\n        \"output\": \" No, Bi3BTeO9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi0.04Te0.06Pb0.98Se0.98\\n\",\n        \"output\": \" No, Bi0.04Te0.06Pb0.98Se0.98 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGa2GeS6\\n\",\n        \"output\": \" No, BaGa2GeS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd2CdIn\\n\",\n        \"output\": \" Yes, Nd2CdIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge40Te5.3I8\\n\",\n        \"output\": \" No, Ge40Te5.3I8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrPd3\\n\",\n        \"output\": \" Yes, ZrPd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TaTiFe2\\n\",\n        \"output\": \" Yes, TaTiFe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2MgGe3Se8\\n\",\n        \"output\": \" No, Cs2MgGe3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HgCl\\n\",\n        \"output\": \" No, HgCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" step\\n\",\n        \"output\": \" step is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KNb2O5\\n\",\n        \"output\": \" Yes, KNb2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li5La3Nb14O42\\n\",\n        \"output\": \" Yes, Li5La3Nb14O42 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl2Mo7O22\\n\",\n        \"output\": \" Yes, Tl2Mo7O22 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2In2SiS6\\n\",\n        \"output\": \" No, Li2In2SiS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaIn2Ir\\n\",\n        \"output\": \" Yes, LaIn2Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2LiFe2N3\\n\",\n        \"output\": \" Yes, Ba2LiFe2N3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2GaAsSe5\\n\",\n        \"output\": \" No, Ba2GaAsSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb3Ga\\n\",\n        \"output\": \" Yes, Rb3Ga is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiAl2Rh\\n\",\n        \"output\": \" Yes, LiAl2Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2Pr2O7\\n\",\n        \"output\": \" Yes, La2Pr2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TiTlSe2\\n\",\n        \"output\": \" No, TiTlSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr0.5Ta1O3\\n\",\n        \"output\": \" No, Sr0.5Ta1O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.9Hg0.1Se1\\n\",\n        \"output\": \" No, Zn0.9Hg0.1Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PbI2\\n\",\n        \"output\": \" No, PbI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InHg7S6Cl5\\n\",\n        \"output\": \" No, InHg7S6Cl5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La3Si1Sb0.33S7\\n\",\n        \"output\": \" No, La3Si1Sb0.33S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Re2W3C\\n\",\n        \"output\": \" Yes, Re2W3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al2Cu\\n\",\n        \"output\": \" Yes, Al2Cu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce2Te3\\n\",\n        \"output\": \" No, Ce2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" direction\\n\",\n        \"output\": \" direction is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti6H2O13\\n\",\n        \"output\": \" No, Ti6H2O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsZrPSe6\\n\",\n        \"output\": \" No, CsZrPSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.002Sb0.998Te0.006\\n\",\n        \"output\": \" No, Ga1.002Sb0.998Te0.006 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KF\\n\",\n        \"output\": \" No, KF is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr2CuS4\\n\",\n        \"output\": \" Yes, Zr2CuS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.8Hg0.2Te1\\n\",\n        \"output\": \" No, Zn0.8Hg0.2Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaSi2\\n\",\n        \"output\": \" No, LaSi2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlNi\\n\",\n        \"output\": \" Yes, TlNi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiScHg2\\n\",\n        \"output\": \" Yes, LiScHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KV6O11\\n\",\n        \"output\": \" Yes, KV6O11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsBiS2\\n\",\n        \"output\": \" No, CsBiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" range\\n\",\n        \"output\": \" range is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc2(PO4)3\\n\",\n        \"output\": \" Yes, Sc2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Cu4NiO8\\n\",\n        \"output\": \" Yes, Li3Cu4NiO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InAsI\\n\",\n        \"output\": \" No, InAsI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K(GeSe2)2\\n\",\n        \"output\": \" No, K(GeSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2(NiO2)3\\n\",\n        \"output\": \" Yes, Li2(NiO2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu2(Ga3Rh)3\\n\",\n        \"output\": \" Yes, Eu2(Ga3Rh)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiS2\\n\",\n        \"output\": \" No, TiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdAg2(PS3)2\\n\",\n        \"output\": \" No, CdAg2(PS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb(Ga4Co)2\\n\",\n        \"output\": \" Yes, Yb(Ga4Co)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf2Ni\\n\",\n        \"output\": \" Yes, Hf2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmTh3\\n\",\n        \"output\": \" Yes, SmTh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu2SnSe5\\n\",\n        \"output\": \" No, Eu2SnSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li(NiO2)4\\n\",\n        \"output\": \" Yes, Li(NiO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y(AlSi)2\\n\",\n        \"output\": \" Yes, Y(AlSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1Hg4As2.5Br3.5\\n\",\n        \"output\": \" No, In1Hg4As2.5Br3.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hg8Bi3As4Cl13\\n\",\n        \"output\": \" No, Hg8Bi3As4Cl13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na15Sn4\\n\",\n        \"output\": \" Yes, Na15Sn4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Eu(BiTe2)2\\n\",\n        \"output\": \" No, Eu(BiTe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfSiPt\\n\",\n        \"output\": \" Yes, HfSiPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Cd3S4\\n\",\n        \"output\": \" No, K2Cd3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li8Ti16CuS32\\n\",\n        \"output\": \" Yes, Li8Ti16CuS32 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3AlP2\\n\",\n        \"output\": \" No, Li3AlP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuTl\\n\",\n        \"output\": \" Yes, EuTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnIn2PbS5\\n\",\n        \"output\": \" No, MnIn2PbS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KIn(TeO3)2\\n\",\n        \"output\": \" No, KIn(TeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Na2IrO4\\n\",\n        \"output\": \" Yes, Rb2Na2IrO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ThIr5\\n\",\n        \"output\": \" Yes, ThIr5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UGa5Ir\\n\",\n        \"output\": \" Yes, UGa5Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmSe\\n\",\n        \"output\": \" No, SmSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ErCuPb\\n\",\n        \"output\": \" Yes, ErCuPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf(CoSi)2\\n\",\n        \"output\": \" Yes, Hf(CoSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrCoGe\\n\",\n        \"output\": \" Yes, CrCoGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaAl12O19\\n\",\n        \"output\": \" Yes, LaAl12O19 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4MgNi3O8\\n\",\n        \"output\": \" Yes, Li4MgNi3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb4Pb4S11\\n\",\n        \"output\": \" Yes, Sb4Pb4S11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlInHgS3\\n\",\n        \"output\": \" No, TlInHgS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaHg\\n\",\n        \"output\": \" Yes, NaHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeOF\\n\",\n        \"output\": \" Yes, FeOF is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" InSb2Se4Br\\n\",\n        \"output\": \" No, InSb2Se4Br is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrAl5Ni2\\n\",\n        \"output\": \" Yes, ZrAl5Ni2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GeSe\\n\",\n        \"output\": \" No, GeSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaIn4Ir\\n\",\n        \"output\": \" Yes, CaIn4Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuCN2\\n\",\n        \"output\": \" Yes, CuCN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy3Al0.5Si1S7\\n\",\n        \"output\": \" No, Dy3Al0.5Si1S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb3Te\\n\",\n        \"output\": \" Yes, Nb3Te is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" specialist\\n\",\n        \"output\": \" specialist is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te0.5Se0.5\\n\",\n        \"output\": \" No, Te0.5Se0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbTe\\n\",\n        \"output\": \" No, YbTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li17Ti20O40\\n\",\n        \"output\": \" Yes, Li17Ti20O40 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca5(Bi7O13)2\\n\",\n        \"output\": \" No, Ca5(Bi7O13)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.001Sb0.999Te0.003\\n\",\n        \"output\": \" No, Ga1.001Sb0.999Te0.003 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K6Cd4Sn3Se13\\n\",\n        \"output\": \" No, K6Cd4Sn3Se13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K6Ta2.93Nb1.07S22\\n\",\n        \"output\": \" No, K6Ta2.93Nb1.07S22 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ThTeO\\n\",\n        \"output\": \" No, ThTeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs3Sn3Cl7F2\\n\",\n        \"output\": \" No, Cs3Sn3Cl7F2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb(IO3)3\\n\",\n        \"output\": \" Yes, Yb(IO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.03Pb0.97Se0.97S0.03\\n\",\n        \"output\": \" No, Ge0.03Pb0.97Se0.97S0.03 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li7(NiO2)11\\n\",\n        \"output\": \" Yes, Li7(NiO2)11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VFeRu2\\n\",\n        \"output\": \" Yes, VFeRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdAgPb\\n\",\n        \"output\": \" Yes, NdAgPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaLa2In2S7\\n\",\n        \"output\": \" No, BaLa2In2S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al10V\\n\",\n        \"output\": \" Yes, Al10V is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mo2NCl8\\n\",\n        \"output\": \" Yes, Mo2NCl8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U2SnRh2\\n\",\n        \"output\": \" Yes, U2SnRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr2HO4\\n\",\n        \"output\": \" Yes, Cr2HO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Te0.6Se2.4\\n\",\n        \"output\": \" No, Bi2Te0.6Se2.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaCuO\\n\",\n        \"output\": \" Yes, NaCuO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr2Co12P7\\n\",\n        \"output\": \" Yes, Zr2Co12P7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrMgIn3\\n\",\n        \"output\": \" Yes, SrMgIn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2CO5\\n\",\n        \"output\": \" No, Bi2CO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm(FeSi)2\\n\",\n        \"output\": \" Yes, Tm(FeSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaInS2O\\n\",\n        \"output\": \" No, LaInS2O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb2EuS4\\n\",\n        \"output\": \" No, Yb2EuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn(PO3)3\\n\",\n        \"output\": \" Yes, Sn(PO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti3SnC2\\n\",\n        \"output\": \" Yes, Ti3SnC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnNiP\\n\",\n        \"output\": \" Yes, MnNiP is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho(SiPd)2\\n\",\n        \"output\": \" Yes, Ho(SiPd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuCuSeF\\n\",\n        \"output\": \" Yes, EuCuSeF is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl3Cr\\n\",\n        \"output\": \" Yes, Tl3Cr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al2CrS4\\n\",\n        \"output\": \" Yes, Al2CrS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Re5(NiAs6)2\\n\",\n        \"output\": \" Yes, Re5(NiAs6)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Co2Te3O8\\n\",\n        \"output\": \" No, Co2Te3O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrGaPt\\n\",\n        \"output\": \" Yes, ZrGaPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2SmInSe5\\n\",\n        \"output\": \" No, Ba2SmInSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li5Fe2Ni3O10\\n\",\n        \"output\": \" Yes, Li5Fe2Ni3O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba1.88Ta15O32\\n\",\n        \"output\": \" No, Ba1.88Ta15O32 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeAl2Pt3\\n\",\n        \"output\": \" Yes, CeAl2Pt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaCd4P3\\n\",\n        \"output\": \" No, NaCd4P3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2VAgS4\\n\",\n        \"output\": \" No, Rb2VAgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" IrS2\\n\",\n        \"output\": \" No, IrS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbSbO3\\n\",\n        \"output\": \" Yes, RbSbO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrTaNO2\\n\",\n        \"output\": \" No, SrTaNO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2TbIrO6\\n\",\n        \"output\": \" Yes, Ba2TbIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2Sn5Rh3\\n\",\n        \"output\": \" Yes, La2Sn5Rh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd2(SnSe3)3\\n\",\n        \"output\": \" No, Nd2(SnSe3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaCuS2\\n\",\n        \"output\": \" No, GaCuS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.005Te1Pb0.995\\n\",\n        \"output\": \" No, In0.005Te1Pb0.995 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlHg6Se4Br5\\n\",\n        \"output\": \" No, TlHg6Se4Br5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb3Ag9(PS4)4\\n\",\n        \"output\": \" No, Rb3Ag9(PS4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr5Al3C\\n\",\n        \"output\": \" Yes, Zr5Al3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KCl\\n\",\n        \"output\": \" No, KCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La4Cd4In2S13\\n\",\n        \"output\": \" No, La4Cd4In2S13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Te0.1Se2.9\\n\",\n        \"output\": \" No, Bi2Te0.1Se2.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu3Sb4Se9\\n\",\n        \"output\": \" No, Eu3Sb4Se9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdIn3\\n\",\n        \"output\": \" Yes, NdIn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4.5Mn0.5Te1O6\\n\",\n        \"output\": \" No, Li4.5Mn0.5Te1O6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce5Ge3\\n\",\n        \"output\": \" Yes, Ce5Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaYbZn2\\n\",\n        \"output\": \" Yes, LaYbZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy3(CuGe)4\\n\",\n        \"output\": \" Yes, Dy3(CuGe)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce(HO)3\\n\",\n        \"output\": \" Yes, Ce(HO)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y(Al2Cu)4\\n\",\n        \"output\": \" Yes, Y(Al2Cu)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbInS2\\n\",\n        \"output\": \" No, RbInS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2TeI6\\n\",\n        \"output\": \" No, Cs2TeI6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsErZnSe3\\n\",\n        \"output\": \" No, CsErZnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KPSe3\\n\",\n        \"output\": \" No, KPSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Pd3S2\\n\",\n        \"output\": \" Yes, Bi2Pd3S2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd13I28\\n\",\n        \"output\": \" Yes, Cd13I28 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Ce(PO4)2\\n\",\n        \"output\": \" No, K2Ce(PO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.01Cd0.99Sb0.01Te0.99\\n\",\n        \"output\": \" No, Al0.01Cd0.99Sb0.01Te0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn2Ni9O13\\n\",\n        \"output\": \" Yes, Zn2Ni9O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf(CuP)2\\n\",\n        \"output\": \" Yes, Hf(CuP)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2MgReO6\\n\",\n        \"output\": \" Yes, Sr2MgReO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(AlAu)2\\n\",\n        \"output\": \" Yes, Eu(AlAu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NbSnIr\\n\",\n        \"output\": \" No, NbSnIr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaTaNO2\\n\",\n        \"output\": \" No, BaTaNO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag2HgI4\\n\",\n        \"output\": \" No, Ag2HgI4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScTa2NO5\\n\",\n        \"output\": \" No, ScTa2NO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbAg2SbS4\\n\",\n        \"output\": \" No, RbAg2SbS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SbOsS\\n\",\n        \"output\": \" No, SbOsS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce4Te7\\n\",\n        \"output\": \" No, Ce4Te7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.5Hg0.5Se1\\n\",\n        \"output\": \" No, Zn0.5Hg0.5Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaCuSe2\\n\",\n        \"output\": \" No, GaCuSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaInSe2\\n\",\n        \"output\": \" No, NaInSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2NdGaS5\\n\",\n        \"output\": \" No, Ba2NdGaS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaP\\n\",\n        \"output\": \" No, LaP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsNa2Sb\\n\",\n        \"output\": \" No, CsNa2Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm2AlOs\\n\",\n        \"output\": \" Yes, Tm2AlOs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbBi3TeSe4\\n\",\n        \"output\": \" No, RbBi3TeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" P2Pt\\n\",\n        \"output\": \" No, P2Pt is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsBi2\\n\",\n        \"output\": \" No, CsBi2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce3TaO7\\n\",\n        \"output\": \" Yes, Ce3TaO7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyCoSi2\\n\",\n        \"output\": \" Yes, DyCoSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" venezuelan\\n\",\n        \"output\": \" venezuelan is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdCuTeO\\n\",\n        \"output\": \" No, NdCuTeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgSbSe2\\n\",\n        \"output\": \" No, AgSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr1.33Ta0.67N1.97O1.38\\n\",\n        \"output\": \" No, Zr1.33Ta0.67N1.97O1.38 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr2Ir2O7\\n\",\n        \"output\": \" Yes, Pr2Ir2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc(TiN)9\\n\",\n        \"output\": \" Yes, Sc(TiN)9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr4InSbSe9\\n\",\n        \"output\": \" No, Pr4InSbSe9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3Bi(PbO4)3\\n\",\n        \"output\": \" No, V3Bi(PbO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb3Sb2Br9\\n\",\n        \"output\": \" No, Rb3Sb2Br9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rh3Pb\\n\",\n        \"output\": \" Yes, Rh3Pb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.5Ga0.5P0.5Se0.5\\n\",\n        \"output\": \" No, Zn0.5Ga0.5P0.5Se0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb2XeF14\\n\",\n        \"output\": \" Yes, Sb2XeF14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbMnTe2\\n\",\n        \"output\": \" Yes, RbMnTe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeAgTe2\\n\",\n        \"output\": \" No, FeAgTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba(NiP2)2\\n\",\n        \"output\": \" Yes, Ba(NiP2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbC8\\n\",\n        \"output\": \" Yes, RbC8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaZnSO\\n\",\n        \"output\": \" No, CaZnSO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd2WC2\\n\",\n        \"output\": \" Yes, Nd2WC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc7CI12\\n\",\n        \"output\": \" Yes, Sc7CI12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" B2O3\\n\",\n        \"output\": \" No, B2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MoO3\\n\",\n        \"output\": \" No, MoO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba4InCuSe6\\n\",\n        \"output\": \" No, Ba4InCuSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuBiSeO\\n\",\n        \"output\": \" No, CuBiSeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlPSe2\\n\",\n        \"output\": \" No, TlPSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScSnPd\\n\",\n        \"output\": \" Yes, ScSnPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy2Ni12P7\\n\",\n        \"output\": \" Yes, Dy2Ni12P7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KZn4(BO3)3\\n\",\n        \"output\": \" No, KZn4(BO3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UGeRh\\n\",\n        \"output\": \" Yes, UGeRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmP\\n\",\n        \"output\": \" No, SmP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.01Cd0.99Se1\\n\",\n        \"output\": \" No, Zn0.01Cd0.99Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TiAlAu2\\n\",\n        \"output\": \" Yes, TiAlAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy2(MoO4)3\\n\",\n        \"output\": \" No, Dy2(MoO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfAlPd2\\n\",\n        \"output\": \" Yes, HfAlPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2MnNi3O8\\n\",\n        \"output\": \" Yes, Li2MnNi3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2O3\\n\",\n        \"output\": \" No, Ga2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BRh2\\n\",\n        \"output\": \" Yes, BRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" capricorn\\n\",\n        \"output\": \" capricorn is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaB6\\n\",\n        \"output\": \" No, LaB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1As0.9P0.1\\n\",\n        \"output\": \" No, Ga1As0.9P0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" USeS\\n\",\n        \"output\": \" Yes, USeS is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In4Cu2Te7\\n\",\n        \"output\": \" No, In4Cu2Te7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThSeO\\n\",\n        \"output\": \" No, ThSeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlGaS2\\n\",\n        \"output\": \" No, TlGaS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2Cu2S3\\n\",\n        \"output\": \" Yes, Li2Cu2S3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.2Ga0.8As1\\n\",\n        \"output\": \" No, In0.2Ga0.8As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbVP2S7\\n\",\n        \"output\": \" Yes, RbVP2S7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Mn3S4\\n\",\n        \"output\": \" Yes, K2Mn3S4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnSe\\n\",\n        \"output\": \" No, MnSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" VAg2I3O11\\n\",\n        \"output\": \" No, VAg2I3O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErAgSn\\n\",\n        \"output\": \" Yes, ErAgSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2CuF6\\n\",\n        \"output\": \" Yes, Li2CuF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga0.07Te1Pb0.93\\n\",\n        \"output\": \" No, Ga0.07Te1Pb0.93 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V6PbO11\\n\",\n        \"output\": \" Yes, V6PbO11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd2Ge5Rh3\\n\",\n        \"output\": \" Yes, Nd2Ge5Rh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbInAg2\\n\",\n        \"output\": \" Yes, TbInAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na6CoSe4\\n\",\n        \"output\": \" Yes, Na6CoSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlN\\n\",\n        \"output\": \" No, TlN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsSb\\n\",\n        \"output\": \" No, CsSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbRh3\\n\",\n        \"output\": \" Yes, SbRh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca2Sn\\n\",\n        \"output\": \" No, Ca2Sn is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2CdSnS4\\n\",\n        \"output\": \" No, Na2CdSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb2Pb2Se4O15\\n\",\n        \"output\": \" No, Nb2Pb2Se4O15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuCo8P5\\n\",\n        \"output\": \" Yes, EuCo8P5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbF3\\n\",\n        \"output\": \" Yes, RbF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn8Ag5\\n\",\n        \"output\": \" Yes, Zn8Ag5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Bi8Se13\\n\",\n        \"output\": \" No, K2Bi8Se13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2MgIn\\n\",\n        \"output\": \" Yes, Li2MgIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li5Mn6(BO3)6\\n\",\n        \"output\": \" Yes, Li5Mn6(BO3)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn3PdN\\n\",\n        \"output\": \" Yes, Mn3PdN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3AlTe4O11\\n\",\n        \"output\": \" No, Li3AlTe4O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuClO\\n\",\n        \"output\": \" Yes, EuClO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KBr\\n\",\n        \"output\": \" No, KBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyInCu2\\n\",\n        \"output\": \" Yes, DyInCu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbAl3\\n\",\n        \"output\": \" Yes, YbAl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaScSi\\n\",\n        \"output\": \" Yes, LaScSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4Mn3Cr3O12\\n\",\n        \"output\": \" Yes, Li4Mn3Cr3O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SbTeRh\\n\",\n        \"output\": \" No, SbTeRh is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsPPbO4\\n\",\n        \"output\": \" No, CsPPbO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsBr\\n\",\n        \"output\": \" No, CsBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AsPd3Pb2\\n\",\n        \"output\": \" Yes, AsPd3Pb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr2Ni12P7\\n\",\n        \"output\": \" Yes, Zr2Ni12P7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KI\\n\",\n        \"output\": \" No, KI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyZnGa\\n\",\n        \"output\": \" Yes, DyZnGa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdGeRu\\n\",\n        \"output\": \" Yes, GdGeRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe2O3\\n\",\n        \"output\": \" No, Fe2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pd(IO3)2\\n\",\n        \"output\": \" No, Pd(IO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cr2NiS4\\n\",\n        \"output\": \" Yes, Cr2NiS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfInCu2\\n\",\n        \"output\": \" Yes, HfInCu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaBi25O39\\n\",\n        \"output\": \" No, GaBi25O39 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.95Ga0.05P0.05Se0.95\\n\",\n        \"output\": \" No, Zn0.95Ga0.05P0.05Se0.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba14Ir8(PdO11)3\\n\",\n        \"output\": \" Yes, Ba14Ir8(PdO11)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn1Se0.2S0.8\\n\",\n        \"output\": \" No, Sn1Se0.2S0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2Ni5B4\\n\",\n        \"output\": \" Yes, La2Ni5B4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr2La2Pt1O7.13\\n\",\n        \"output\": \" No, Sr2La2Pt1O7.13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn3P2\\n\",\n        \"output\": \" No, Zn3P2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al0.75Ga0.25As1\\n\",\n        \"output\": \" No, Al0.75Ga0.25As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RhSe2\\n\",\n        \"output\": \" No, RhSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd(InSe2)2\\n\",\n        \"output\": \" No, Cd(InSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In5Se6\\n\",\n        \"output\": \" No, In5Se6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrFeGe2\\n\",\n        \"output\": \" Yes, PrFeGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr4Ga8Ge15\\n\",\n        \"output\": \" No, Sr4Ga8Ge15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rh2S3\\n\",\n        \"output\": \" No, Rh2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" USi3\\n\",\n        \"output\": \" Yes, USi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Th2CrN3\\n\",\n        \"output\": \" Yes, Th2CrN3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaYb(PS3)2\\n\",\n        \"output\": \" No, NaYb(PS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbSbTe2\\n\",\n        \"output\": \" No, RbSbTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" InCuTe2\\n\",\n        \"output\": \" No, InCuTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.2Te0.2Pb0.8Se0.8\\n\",\n        \"output\": \" No, Ge0.2Te0.2Pb0.8Se0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd12Ge17(B4O29)2\\n\",\n        \"output\": \" No, Cd12Ge17(B4O29)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdP4PbO12\\n\",\n        \"output\": \" No, CdP4PbO12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaGa3Pd2\\n\",\n        \"output\": \" Yes, LaGa3Pd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb2Ce8O19\\n\",\n        \"output\": \" Yes, Yb2Ce8O19 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb(MnGe)6\\n\",\n        \"output\": \" Yes, Tb(MnGe)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li5Fe6(BO3)6\\n\",\n        \"output\": \" Yes, Li5Fe6(BO3)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" U2MnN3\\n\",\n        \"output\": \" Yes, U2MnN3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGa2SiSe6\\n\",\n        \"output\": \" No, BaGa2SiSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrAlW\\n\",\n        \"output\": \" Yes, ZrAlW is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2HgGeS4\\n\",\n        \"output\": \" No, Li2HgGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2NaVF6\\n\",\n        \"output\": \" Yes, Rb2NaVF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Ni2(GeO4)3\\n\",\n        \"output\": \" Yes, Li3Ni2(GeO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr8(MnN3)3\\n\",\n        \"output\": \" Yes, Sr8(MnN3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.2Ga0.8As0.8P0.2\\n\",\n        \"output\": \" No, In0.2Ga0.8As0.8P0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd3Bi2\\n\",\n        \"output\": \" No, Cd3Bi2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm3GaC\\n\",\n        \"output\": \" Yes, Tm3GaC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy3InC\\n\",\n        \"output\": \" Yes, Dy3InC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnSnSb2\\n\",\n        \"output\": \" No, ZnSnSb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg2Si\\n\",\n        \"output\": \" No, Mg2Si is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In3CuSe5\\n\",\n        \"output\": \" No, In3CuSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeSiOs\\n\",\n        \"output\": \" Yes, CeSiOs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd3In\\n\",\n        \"output\": \" Yes, Nd3In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaCdPd2\\n\",\n        \"output\": \" Yes, CaCdPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" mattock\\n\",\n        \"output\": \" mattock is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmSnRu2\\n\",\n        \"output\": \" Yes, TmSnRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaNa2GeSe4\\n\",\n        \"output\": \" No, BaNa2GeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KH3(SeO3)2\\n\",\n        \"output\": \" No, KH3(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErB6\\n\",\n        \"output\": \" No, ErB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmHoHg2\\n\",\n        \"output\": \" Yes, SmHoHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HoTlPd\\n\",\n        \"output\": \" Yes, HoTlPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrAu4\\n\",\n        \"output\": \" Yes, ZrAu4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" statement\\n\",\n        \"output\": \" statement is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" century\\n\",\n        \"output\": \" century is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmCo3B2\\n\",\n        \"output\": \" Yes, SmCo3B2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Co3SbO8\\n\",\n        \"output\": \" Yes, Li3Co3SbO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn(CuO2)2\\n\",\n        \"output\": \" Yes, Zn(CuO2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrNiGe2\\n\",\n        \"output\": \" Yes, PrNiGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiReN3\\n\",\n        \"output\": \" Yes, TiReN3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba4Ga4SnSe12\\n\",\n        \"output\": \" No, Ba4Ga4SnSe12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AsI3\\n\",\n        \"output\": \" No, AsI3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScGa2\\n\",\n        \"output\": \" Yes, ScGa2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3(OsO5)2\\n\",\n        \"output\": \" Yes, La3(OsO5)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2NbCuSe4\\n\",\n        \"output\": \" No, Cs2NbCuSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThAsSe\\n\",\n        \"output\": \" Yes, ThAsSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K3(FeS2)2\\n\",\n        \"output\": \" Yes, K3(FeS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3MnAs2\\n\",\n        \"output\": \" Yes, Li3MnAs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KCu2SbS3\\n\",\n        \"output\": \" No, KCu2SbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy(Al2Cu)4\\n\",\n        \"output\": \" Yes, Dy(Al2Cu)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm3(GePd)4\\n\",\n        \"output\": \" Yes, Tm3(GePd)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlCr5Se8\\n\",\n        \"output\": \" No, TlCr5Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" windshield\\n\",\n        \"output\": \" windshield is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiGaAu2\\n\",\n        \"output\": \" Yes, LiGaAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiMn4O8\\n\",\n        \"output\": \" Yes, LiMn4O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb3Cd(BO2)5\\n\",\n        \"output\": \" No, Rb3Cd(BO2)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrCdSi\\n\",\n        \"output\": \" Yes, SrCdSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1As0.99P0.01\\n\",\n        \"output\": \" No, Ga1As0.99P0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsMg149\\n\",\n        \"output\": \" Yes, CsMg149 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnCu2SnTe4\\n\",\n        \"output\": \" No, ZnCu2SnTe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BeCu\\n\",\n        \"output\": \" Yes, BeCu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuSn3\\n\",\n        \"output\": \" Yes, EuSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsH3(SeO3)2\\n\",\n        \"output\": \" No, CsH3(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlAgO2\\n\",\n        \"output\": \" No, AlAgO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm2ZnGa\\n\",\n        \"output\": \" Yes, Tm2ZnGa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaAsO3\\n\",\n        \"output\": \" Yes, NaAsO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VIn(NiO3)2\\n\",\n        \"output\": \" No, VIn(NiO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3Zr17O37\\n\",\n        \"output\": \" Yes, Ca3Zr17O37 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sb3IO4\\n\",\n        \"output\": \" No, Sb3IO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd(In15Te23)2\\n\",\n        \"output\": \" No, Cd(In15Te23)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.458Ge0.542\\n\",\n        \"output\": \" No, Si0.458Ge0.542 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuIn2(GeIr)4\\n\",\n        \"output\": \" No, EuIn2(GeIr)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlHg6S4Br5\\n\",\n        \"output\": \" No, TlHg6S4Br5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbCd4Ga5Se12\\n\",\n        \"output\": \" No, RbCd4Ga5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti5ZnO7\\n\",\n        \"output\": \" Yes, Ti5ZnO7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3FeS4Br\\n\",\n        \"output\": \" No, Ba3FeS4Br is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2MnSnSe4\\n\",\n        \"output\": \" No, K2MnSnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuH2\\n\",\n        \"output\": \" No, EuH2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3(CoO2)4\\n\",\n        \"output\": \" Yes, Li3(CoO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd1Se0.2S0.8\\n\",\n        \"output\": \" No, Cd1Se0.2S0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2PdO4\\n\",\n        \"output\": \" Yes, La2PdO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te0.8Se0.2\\n\",\n        \"output\": \" No, Te0.8Se0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr3Ag\\n\",\n        \"output\": \" Yes, Zr3Ag is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2VCuS4\\n\",\n        \"output\": \" No, K2VCuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba5Ga6GeP12\\n\",\n        \"output\": \" No, Ba5Ga6GeP12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.8Ga0.2As0.2P0.8\\n\",\n        \"output\": \" No, In0.8Ga0.2As0.2P0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2PmGe\\n\",\n        \"output\": \" Yes, Li2PmGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2SmP2S7\\n\",\n        \"output\": \" No, K2SmP2S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaZnSiSe4\\n\",\n        \"output\": \" No, BaZnSiSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" As2Ru\\n\",\n        \"output\": \" No, As2Ru is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg2TcO4\\n\",\n        \"output\": \" Yes, Mg2TcO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScCoGe2\\n\",\n        \"output\": \" Yes, ScCoGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaLa2CoS5\\n\",\n        \"output\": \" Yes, BaLa2CoS5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TaNO\\n\",\n        \"output\": \" No, TaNO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdLuSe3\\n\",\n        \"output\": \" No, NdLuSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y2S3\\n\",\n        \"output\": \" No, Y2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.99Ga0.01P1\\n\",\n        \"output\": \" No, Al0.99Ga0.01P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgIn3\\n\",\n        \"output\": \" Yes, MgIn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrGeRu\\n\",\n        \"output\": \" Yes, ZrGeRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaTe\\n\",\n        \"output\": \" No, CaTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr2HoRuO6\\n\",\n        \"output\": \" Yes, Sr2HoRuO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3Co10O17\\n\",\n        \"output\": \" Yes, Ba3Co10O17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeAsSe\\n\",\n        \"output\": \" Yes, CeAsSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Ta2Se9\\n\",\n        \"output\": \" No, Ba3Ta2Se9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2Hg(PSe3)2\\n\",\n        \"output\": \" No, Rb2Hg(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho2GeS5\\n\",\n        \"output\": \" No, Ho2GeS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbUAgS3\\n\",\n        \"output\": \" Yes, RbUAgS3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta3P\\n\",\n        \"output\": \" Yes, Ta3P is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2NbCuS4\\n\",\n        \"output\": \" No, K2NbCuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm(InS2)3\\n\",\n        \"output\": \" No, Sm(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd2BC\\n\",\n        \"output\": \" Yes, Nd2BC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YCoO3\\n\",\n        \"output\": \" Yes, YCoO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag7AsS6\\n\",\n        \"output\": \" No, Ag7AsS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2B6O11\\n\",\n        \"output\": \" No, Ba2B6O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pb2SeN2O9\\n\",\n        \"output\": \" No, Pb2SeN2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiThAu2\\n\",\n        \"output\": \" Yes, LiThAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiYbPb\\n\",\n        \"output\": \" Yes, LiYbPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" rub\\n\",\n        \"output\": \" rub is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3Ag2(SnS4)2\\n\",\n        \"output\": \" No, Ba3Ag2(SnS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y2Mo2O7\\n\",\n        \"output\": \" Yes, Y2Mo2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2Zn3(SeO3)4\\n\",\n        \"output\": \" No, Rb2Zn3(SeO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba5V3O12F\\n\",\n        \"output\": \" No, Ba5V3O12F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2ReRh\\n\",\n        \"output\": \" Yes, Ti2ReRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu2Te3O8\\n\",\n        \"output\": \" No, Cu2Te3O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1.02Sb0.98Te0.06\\n\",\n        \"output\": \" No, Ga1.02Sb0.98Te0.06 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.05Pb0.95Se0.95S0.05\\n\",\n        \"output\": \" No, Ge0.05Pb0.95Se0.95S0.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb(Al2Mo)2\\n\",\n        \"output\": \" Yes, Yb(Al2Mo)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cr4Cu3Te8\\n\",\n        \"output\": \" Yes, Cr4Cu3Te8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1Ga1Cu1S3.5\\n\",\n        \"output\": \" No, In1Ga1Cu1S3.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ni3SnN\\n\",\n        \"output\": \" Yes, Ni3SnN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy4GaSbS9\\n\",\n        \"output\": \" No, Dy4GaSbS9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" break\\n\",\n        \"output\": \" break is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaVI5O16\\n\",\n        \"output\": \" No, LaVI5O16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr(CeS2)2\\n\",\n        \"output\": \" Yes, Sr(CeS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V2NO\\n\",\n        \"output\": \" Yes, V2NO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbY(TeO3)2\\n\",\n        \"output\": \" No, RbY(TeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeAsS\\n\",\n        \"output\": \" No, FeAsS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Cr7O14\\n\",\n        \"output\": \" Yes, Na2Cr7O14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbTeOs\\n\",\n        \"output\": \" No, SbTeOs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2Ce2O5\\n\",\n        \"output\": \" Yes, Ba2Ce2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeSn\\n\",\n        \"output\": \" Yes, FeSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrCrO4\\n\",\n        \"output\": \" No, SrCrO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K3Sm(AsS4)2\\n\",\n        \"output\": \" No, K3Sm(AsS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2Fe2(PO4)3\\n\",\n        \"output\": \" Yes, Li2Fe2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(BiSe2)2\\n\",\n        \"output\": \" No, Eu(BiSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3GaTe4O11\\n\",\n        \"output\": \" No, Li3GaTe4O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbNd2CuS5\\n\",\n        \"output\": \" No, YbNd2CuS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga2PbS4\\n\",\n        \"output\": \" No, Ga2PbS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf2OsPd\\n\",\n        \"output\": \" Yes, Hf2OsPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr3ScNiO6\\n\",\n        \"output\": \" Yes, Sr3ScNiO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2CuWO6\\n\",\n        \"output\": \" Yes, Ba2CuWO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NiN\\n\",\n        \"output\": \" Yes, NiN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Mo2P5O18\\n\",\n        \"output\": \" Yes, Li3Mo2P5O18 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K3V\\n\",\n        \"output\": \" Yes, K3V is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Te1.2Se1.8\\n\",\n        \"output\": \" No, Bi2Te1.2Se1.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si2Pd9\\n\",\n        \"output\": \" Yes, Si2Pd9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2In2P3Se10\\n\",\n        \"output\": \" No, K2In2P3Se10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2In3AgSe6\\n\",\n        \"output\": \" No, K2In3AgSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoC2\\n\",\n        \"output\": \" Yes, HoC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnCu2SnSe4\\n\",\n        \"output\": \" No, ZnCu2SnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hg3Bi2(TeCl4)2\\n\",\n        \"output\": \" No, Hg3Bi2(TeCl4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag(W3Br7)2\\n\",\n        \"output\": \" Yes, Ag(W3Br7)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScCuO2\\n\",\n        \"output\": \" No, ScCuO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiMnCuO4\\n\",\n        \"output\": \" Yes, LiMnCuO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdAs\\n\",\n        \"output\": \" No, NdAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La3Te4\\n\",\n        \"output\": \" No, La3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr8.007Ge2.043Bi7.949Se24\\n\",\n        \"output\": \" No, Sr8.007Ge2.043Bi7.949Se24 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi0.4Sb1.6Te3\\n\",\n        \"output\": \" No, Bi0.4Sb1.6Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag2S\\n\",\n        \"output\": \" No, Ag2S is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb5Ge3\\n\",\n        \"output\": \" Yes, Nb5Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr2CdSn\\n\",\n        \"output\": \" Yes, Pr2CdSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TiAl\\n\",\n        \"output\": \" Yes, TiAl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf4Al3\\n\",\n        \"output\": \" Yes, Hf4Al3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuAl2Pd5\\n\",\n        \"output\": \" Yes, LuAl2Pd5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl(MoSe)3\\n\",\n        \"output\": \" Yes, Tl(MoSe)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YSbPd\\n\",\n        \"output\": \" No, YSbPd is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag3AsO4\\n\",\n        \"output\": \" Yes, Ag3AsO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn(InTe2)2\\n\",\n        \"output\": \" No, Zn(InTe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba4Ga5CuSe12\\n\",\n        \"output\": \" No, Ba4Ga5CuSe12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ReO3\\n\",\n        \"output\": \" No, ReO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaTl(MoO3)2\\n\",\n        \"output\": \" Yes, BaTl(MoO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu4Sn7S16\\n\",\n        \"output\": \" No, Cu4Sn7S16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiCuO2\\n\",\n        \"output\": \" Yes, LiCuO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2AgRu\\n\",\n        \"output\": \" Yes, Sm2AgRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" U4N7\\n\",\n        \"output\": \" Yes, U4N7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VCo\\n\",\n        \"output\": \" Yes, VCo is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeAsPd\\n\",\n        \"output\": \" Yes, CeAsPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdIClO3\\n\",\n        \"output\": \" No, CdIClO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuTe\\n\",\n        \"output\": \" No, EuTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti3Cu3O\\n\",\n        \"output\": \" Yes, Ti3Cu3O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn2WO5\\n\",\n        \"output\": \" No, Sn2WO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta2OsW\\n\",\n        \"output\": \" Yes, Ta2OsW is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.55Hg0.45Se1\\n\",\n        \"output\": \" No, Zn0.55Hg0.45Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd3In2(Te2S)2\\n\",\n        \"output\": \" No, Cd3In2(Te2S)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaAu2\\n\",\n        \"output\": \" Yes, BaAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnGeAs2\\n\",\n        \"output\": \" No, ZnGeAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu9Se4(Cl3O7)2\\n\",\n        \"output\": \" Yes, Cu9Se4(Cl3O7)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm3AlN\\n\",\n        \"output\": \" Yes, Sm3AlN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2Co5B2\\n\",\n        \"output\": \" Yes, Ce2Co5B2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BeO\\n\",\n        \"output\": \" No, BeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsTiF4\\n\",\n        \"output\": \" Yes, CsTiF4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScCrO4\\n\",\n        \"output\": \" Yes, ScCrO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Hg3Se1.31S2.69\\n\",\n        \"output\": \" No, K2Hg3Se1.31S2.69 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrTl2\\n\",\n        \"output\": \" Yes, SrTl2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na6FeS4\\n\",\n        \"output\": \" Yes, Na6FeS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ReSe2\\n\",\n        \"output\": \" No, ReSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiFe2Si\\n\",\n        \"output\": \" No, TiFe2Si is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Se\\n\",\n        \"output\": \" No, K2Se is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd2InCuTe4\\n\",\n        \"output\": \" No, Cd2InCuTe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4WO5\\n\",\n        \"output\": \" Yes, Li4WO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrNi5As3\\n\",\n        \"output\": \" Yes, SrNi5As3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaPt5\\n\",\n        \"output\": \" Yes, BaPt5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2U(MoO5)2\\n\",\n        \"output\": \" Yes, Li2U(MoO5)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KAg2AsS3\\n\",\n        \"output\": \" No, KAg2AsS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiEuH3\\n\",\n        \"output\": \" No, LiEuH3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca(PrS2)2\\n\",\n        \"output\": \" No, Ca(PrS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScNiSb\\n\",\n        \"output\": \" No, ScNiSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf2Ge\\n\",\n        \"output\": \" Yes, Hf2Ge is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2SnSe5\\n\",\n        \"output\": \" No, Ba2SnSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy1Te1.4\\n\",\n        \"output\": \" No, Dy1Te1.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfGaCo2\\n\",\n        \"output\": \" Yes, HfGaCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiLu2Tc\\n\",\n        \"output\": \" Yes, LiLu2Tc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rh7(PbO5)3\\n\",\n        \"output\": \" Yes, Rh7(PbO5)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd(GePt)2\\n\",\n        \"output\": \" Yes, Nd(GePt)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdTlAg2\\n\",\n        \"output\": \" Yes, NdTlAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg17Al11Pd\\n\",\n        \"output\": \" Yes, Mg17Al11Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TeWCl9\\n\",\n        \"output\": \" Yes, TeWCl9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Co5Ge7\\n\",\n        \"output\": \" Yes, Co5Ge7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Gd3(AlNi3)2\\n\",\n        \"output\": \" Yes, Gd3(AlNi3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.347Ge0.653\\n\",\n        \"output\": \" No, Si0.347Ge0.653 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsInSe2\\n\",\n        \"output\": \" No, CsInSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li7(Mo3S4)4\\n\",\n        \"output\": \" Yes, Li7(Mo3S4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2CrCl4\\n\",\n        \"output\": \" Yes, Cs2CrCl4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2NaCu3S5\\n\",\n        \"output\": \" No, Ba2NaCu3S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoInAu2\\n\",\n        \"output\": \" Yes, HoInAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuSnTe2\\n\",\n        \"output\": \" No, EuSnTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2YbPb\\n\",\n        \"output\": \" Yes, Li2YbPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbRuSe\\n\",\n        \"output\": \" No, SbRuSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeBiW2O9\\n\",\n        \"output\": \" No, CeBiW2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScSbRh2\\n\",\n        \"output\": \" Yes, ScSbRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm2Se3\\n\",\n        \"output\": \" No, Sm2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsSmHgSe3\\n\",\n        \"output\": \" No, CsSmHgSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoTiSi\\n\",\n        \"output\": \" Yes, HoTiSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Gd1.87Lu2.13Se6\\n\",\n        \"output\": \" No, Gd1.87Lu2.13Se6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiSb3PbS6\\n\",\n        \"output\": \" No, LiSb3PbS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrIr2\\n\",\n        \"output\": \" Yes, ZrIr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn2Sb3O8\\n\",\n        \"output\": \" Yes, Zn2Sb3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.94Ge0.06\\n\",\n        \"output\": \" No, Si0.94Ge0.06 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsLi(B3O5)2\\n\",\n        \"output\": \" No, CsLi(B3O5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmBRh3\\n\",\n        \"output\": \" Yes, TmBRh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuSi2Ni\\n\",\n        \"output\": \" Yes, LuSi2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K1.25Bi7.25Pb3.5Se15\\n\",\n        \"output\": \" No, K1.25Bi7.25Pb3.5Se15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmSb\\n\",\n        \"output\": \" No, SmSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.99Hg0.01Se1\\n\",\n        \"output\": \" No, Cd0.99Hg0.01Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlAgSe2\\n\",\n        \"output\": \" No, TlAgSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(ZnSi)2\\n\",\n        \"output\": \" Yes, Eu(ZnSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdSb2Se3Br2\\n\",\n        \"output\": \" No, CdSb2Se3Br2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlCdS2\\n\",\n        \"output\": \" No, TlCdS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaAgGeS4\\n\",\n        \"output\": \" No, GaAgGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ox\\n\",\n        \"output\": \" ox is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyGe\\n\",\n        \"output\": \" Yes, DyGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb6U3O17\\n\",\n        \"output\": \" Yes, Yb6U3O17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2YInTe5\\n\",\n        \"output\": \" No, Ba2YInTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li7Ti7O16\\n\",\n        \"output\": \" Yes, Li7Ti7O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbF\\n\",\n        \"output\": \" No, RbF is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrTmTl2\\n\",\n        \"output\": \" Yes, PrTmTl2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoCu4Pd\\n\",\n        \"output\": \" Yes, HoCu4Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuI\\n\",\n        \"output\": \" No, CuI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K2Mn(SnSe3)2\\n\",\n        \"output\": \" No, K2Mn(SnSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ta6Ni16Ge7\\n\",\n        \"output\": \" Yes, Ta6Ni16Ge7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2TcRu\\n\",\n        \"output\": \" Yes, V2TcRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CdTe\\n\",\n        \"output\": \" No, CdTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2DyGaTe5\\n\",\n        \"output\": \" No, Ba2DyGaTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2NbCuSe4\\n\",\n        \"output\": \" No, K2NbCuSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeLu3\\n\",\n        \"output\": \" Yes, CeLu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.1Te1Pb0.9\\n\",\n        \"output\": \" No, Ge0.1Te1Pb0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgCuSn\\n\",\n        \"output\": \" Yes, MgCuSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SiGe\\n\",\n        \"output\": \" No, SiGe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2Pb4(Se2O7)3\\n\",\n        \"output\": \" No, V2Pb4(Se2O7)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbSi2Ni\\n\",\n        \"output\": \" Yes, YbSi2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2NdInTe5\\n\",\n        \"output\": \" No, Ba2NdInTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnCu2GeS4\\n\",\n        \"output\": \" No, ZnCu2GeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs5P5Se12\\n\",\n        \"output\": \" No, Cs5P5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ta2PtSe7\\n\",\n        \"output\": \" Yes, Ta2PtSe7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na0.75Eu1.625Ge1Se4\\n\",\n        \"output\": \" No, Na0.75Eu1.625Ge1Se4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.1Cd0.9Sb0.1Te0.9\\n\",\n        \"output\": \" No, Al0.1Cd0.9Sb0.1Te0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm5Br11\\n\",\n        \"output\": \" Yes, Sm5Br11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu4As2O9\\n\",\n        \"output\": \" Yes, Cu4As2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbAgO2\\n\",\n        \"output\": \" Yes, YbAgO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb(CuTe)3\\n\",\n        \"output\": \" No, Tb(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.02Te0.98Pb0.98S0.02\\n\",\n        \"output\": \" No, Ge0.02Te0.98Pb0.98S0.02 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AsSeBr\\n\",\n        \"output\": \" Yes, AsSeBr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Co3Se4\\n\",\n        \"output\": \" Yes, Co3Se4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrTaN2O\\n\",\n        \"output\": \" No, PrTaN2O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2TeWO6\\n\",\n        \"output\": \" No, Li2TeWO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SiBi3O7\\n\",\n        \"output\": \" Yes, SiBi3O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" journey\\n\",\n        \"output\": \" journey is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho2HfS5\\n\",\n        \"output\": \" No, Ho2HfS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiFe2(PO4)3\\n\",\n        \"output\": \" Yes, LiFe2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd3Te4\\n\",\n        \"output\": \" No, Nd3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce9SmO20\\n\",\n        \"output\": \" Yes, Ce9SmO20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ReS2\\n\",\n        \"output\": \" No, ReS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd3S4\\n\",\n        \"output\": \" Yes, Gd3S4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.6Ga0.4As0.6P0.4\\n\",\n        \"output\": \" No, In0.6Ga0.4As0.6P0.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbSeI\\n\",\n        \"output\": \" No, SbSeI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(GaSe2)2\\n\",\n        \"output\": \" No, Eu(GaSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaGe2\\n\",\n        \"output\": \" Yes, CaGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsBiSe2\\n\",\n        \"output\": \" No, CsBiSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrTl2InSe4\\n\",\n        \"output\": \" No, PrTl2InSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.01In0.99Te0.01As0.99\\n\",\n        \"output\": \" No, Cd0.01In0.99Te0.01As0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbSbSe2\\n\",\n        \"output\": \" No, RbSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li8PrO6\\n\",\n        \"output\": \" Yes, Li8PrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlAsSe2\\n\",\n        \"output\": \" No, TlAsSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(InSe2)2\\n\",\n        \"output\": \" No, Eu(InSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.01Pb0.99Se1\\n\",\n        \"output\": \" No, Sn0.01Pb0.99Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl4CuTeO6\\n\",\n        \"output\": \" No, Tl4CuTeO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr6Sb2Pt\\n\",\n        \"output\": \" Yes, Zr6Sb2Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.5Ga0.5As1\\n\",\n        \"output\": \" No, In0.5Ga0.5As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PH2NO2\\n\",\n        \"output\": \" Yes, PH2NO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu2Te\\n\",\n        \"output\": \" No, Cu2Te is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnS\\n\",\n        \"output\": \" Yes, MnS is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmAl4Ni\\n\",\n        \"output\": \" Yes, TmAl4Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga2Se3\\n\",\n        \"output\": \" No, Ga2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K1.83Cd1.83Bi2.17S6\\n\",\n        \"output\": \" No, K1.83Cd1.83Bi2.17S6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc2FeB2Ir5\\n\",\n        \"output\": \" Yes, Sc2FeB2Ir5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In3AgTe5\\n\",\n        \"output\": \" No, In3AgTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm2ZnAg\\n\",\n        \"output\": \" Yes, Tm2ZnAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlSnAuSe3\\n\",\n        \"output\": \" No, TlSnAuSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs39Ga53(Se16Cl)6\\n\",\n        \"output\": \" No, Cs39Ga53(Se16Cl)6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InAgSe2\\n\",\n        \"output\": \" No, InAgSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li12Fe5O16\\n\",\n        \"output\": \" Yes, Li12Fe5O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuGe3Pt\\n\",\n        \"output\": \" Yes, EuGe3Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" sand\\n\",\n        \"output\": \" sand is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GdNiO3\\n\",\n        \"output\": \" Yes, GdNiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlSbSe2\\n\",\n        \"output\": \" No, TlSbSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2Hg6(P2Cl3)3\\n\",\n        \"output\": \" No, In2Hg6(P2Cl3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf5Sb3\\n\",\n        \"output\": \" Yes, Hf5Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti2Cd\\n\",\n        \"output\": \" Yes, Ti2Cd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho3Hg\\n\",\n        \"output\": \" Yes, Ho3Hg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlCuTe2\\n\",\n        \"output\": \" No, AlCuTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2ThCu2Se5\\n\",\n        \"output\": \" No, Ba2ThCu2Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2S\\n\",\n        \"output\": \" No, Tl2S is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.005Sb0.995Se0.015\\n\",\n        \"output\": \" No, Ga1.005Sb0.995Se0.015 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" P2O5\\n\",\n        \"output\": \" Yes, P2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Mn\\n\",\n        \"output\": \" Yes, Rb3Mn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1Sb0.99As0.01\\n\",\n        \"output\": \" No, Ga1Sb0.99As0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.1Ga0.9Sb0.9Te0.1\\n\",\n        \"output\": \" No, Cd0.1Ga0.9Sb0.9Te0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu2GeS3\\n\",\n        \"output\": \" No, Cu2GeS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr5Si4\\n\",\n        \"output\": \" Yes, Pr5Si4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.204Hg0.796Te1\\n\",\n        \"output\": \" No, Cd0.204Hg0.796Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg5B3O9F\\n\",\n        \"output\": \" No, Mg5B3O9F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrNiGe\\n\",\n        \"output\": \" Yes, ZrNiGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BeSiOs2\\n\",\n        \"output\": \" Yes, BeSiOs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KEuAsS4\\n\",\n        \"output\": \" No, KEuAsS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2Ti(CuS2)2\\n\",\n        \"output\": \" No, Rb2Ti(CuS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuNiBC\\n\",\n        \"output\": \" Yes, LuNiBC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CoPS\\n\",\n        \"output\": \" No, CoPS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In2Bi3Se7I\\n\",\n        \"output\": \" No, In2Bi3Se7I is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KCuSnS3\\n\",\n        \"output\": \" No, KCuSnS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Co2B4Mo\\n\",\n        \"output\": \" Yes, Co2B4Mo is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmCuSi\\n\",\n        \"output\": \" Yes, TmCuSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmCoSi2\\n\",\n        \"output\": \" Yes, TmCoSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmCuSeO\\n\",\n        \"output\": \" No, SmCuSeO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmCrGe3\\n\",\n        \"output\": \" Yes, SmCrGe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb5(W4O15)2\\n\",\n        \"output\": \" Yes, Rb5(W4O15)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaIn(TeO3)2\\n\",\n        \"output\": \" No, NaIn(TeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.01Ga0.99P0.99Se0.01\\n\",\n        \"output\": \" No, Zn0.01Ga0.99P0.99Se0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr6Nb7O21\\n\",\n        \"output\": \" Yes, Sr6Nb7O21 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlS2\\n\",\n        \"output\": \" No, TlS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb4Ge3B6O17\\n\",\n        \"output\": \" No, Rb4Ge3B6O17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba4Yb(CuO3)3\\n\",\n        \"output\": \" Yes, Ba4Yb(CuO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr5Cd2Sb5F\\n\",\n        \"output\": \" Yes, Sr5Cd2Sb5F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErB2Ir3\\n\",\n        \"output\": \" Yes, ErB2Ir3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HPbI3\\n\",\n        \"output\": \" Yes, HPbI3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca5Ir\\n\",\n        \"output\": \" Yes, Ca5Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hf3(NiGe)4\\n\",\n        \"output\": \" Yes, Hf3(NiGe)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs4Ga4Si19\\n\",\n        \"output\": \" No, Cs4Ga4Si19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb0.52Pr2.48Ga1.67S7\\n\",\n        \"output\": \" No, Tb0.52Pr2.48Ga1.67S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScIr\\n\",\n        \"output\": \" Yes, ScIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaIn3S5\\n\",\n        \"output\": \" No, NaIn3S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm(CuS)2\\n\",\n        \"output\": \" Yes, Tm(CuS)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YB66\\n\",\n        \"output\": \" No, YB66 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te2Mo3Se4\\n\",\n        \"output\": \" Yes, Te2Mo3Se4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr6Al2CoH10\\n\",\n        \"output\": \" Yes, Zr6Al2CoH10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2MnN2\\n\",\n        \"output\": \" Yes, Mg2MnN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsAg5Te3\\n\",\n        \"output\": \" No, CsAg5Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GdB6\\n\",\n        \"output\": \" No, GdB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Ga(GeSe3)2\\n\",\n        \"output\": \" No, Li2Ga(GeSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsF\\n\",\n        \"output\": \" No, CsF is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Cd(GeSe3)2\\n\",\n        \"output\": \" No, Na2Cd(GeSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.15Ga0.85As0.85Se0.15\\n\",\n        \"output\": \" No, Zn0.15Ga0.85As0.85Se0.15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaB6\\n\",\n        \"output\": \" No, BaB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti2AlV\\n\",\n        \"output\": \" Yes, Ti2AlV is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaNa2SnS4\\n\",\n        \"output\": \" No, BaNa2SnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrSb\\n\",\n        \"output\": \" Yes, ZrSb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba7Ga5AgS15\\n\",\n        \"output\": \" No, Ba7Ga5AgS15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Cu(PS3)3\\n\",\n        \"output\": \" No, Cs2Cu(PS3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TaBe2\\n\",\n        \"output\": \" Yes, TaBe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2AgSnSe4\\n\",\n        \"output\": \" No, K2AgSnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Te3\\n\",\n        \"output\": \" No, Bi2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3BSbS6\\n\",\n        \"output\": \" No, Ba3BSbS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" U6Co\\n\",\n        \"output\": \" Yes, U6Co is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnWO2\\n\",\n        \"output\": \" Yes, ZnWO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" FeI2\\n\",\n        \"output\": \" No, FeI2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd6P7\\n\",\n        \"output\": \" No, Cd6P7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd1Se0.45S0.55\\n\",\n        \"output\": \" No, Cd1Se0.45S0.55 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BiTeNO6\\n\",\n        \"output\": \" No, BiTeNO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrInCu2\\n\",\n        \"output\": \" Yes, ZrInCu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" deal\\n\",\n        \"output\": \" deal is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4Ni3BiO8\\n\",\n        \"output\": \" Yes, Li4Ni3BiO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2.35Sb8.65Se14\\n\",\n        \"output\": \" No, Tl2.35Sb8.65Se14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsAu\\n\",\n        \"output\": \" No, CsAu is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm4InSbS9\\n\",\n        \"output\": \" No, Sm4InSbS9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr2HBr2\\n\",\n        \"output\": \" Yes, Zr2HBr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YTi4(CuO4)3\\n\",\n        \"output\": \" Yes, YTi4(CuO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnFeAs\\n\",\n        \"output\": \" Yes, MnFeAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" sweatshop\\n\",\n        \"output\": \" sweatshop is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CrSb2\\n\",\n        \"output\": \" No, CrSb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TiFeH2\\n\",\n        \"output\": \" Yes, TiFeH2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2Cu2SnS4\\n\",\n        \"output\": \" No, Rb2Cu2SnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VTc\\n\",\n        \"output\": \" Yes, VTc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KAlGeS4\\n\",\n        \"output\": \" No, KAlGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyAs\\n\",\n        \"output\": \" No, DyAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PbBr2\\n\",\n        \"output\": \" No, PbBr2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KInSe2\\n\",\n        \"output\": \" No, KInSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ag2BBr\\n\",\n        \"output\": \" Yes, Ag2BBr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K4GeS4\\n\",\n        \"output\": \" No, K4GeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdCu3(RuO3)4\\n\",\n        \"output\": \" Yes, NdCu3(RuO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy4CdRh\\n\",\n        \"output\": \" Yes, Dy4CdRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiClO\\n\",\n        \"output\": \" No, BiClO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdSiP2\\n\",\n        \"output\": \" No, CdSiP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K4(ZrSe5)3\\n\",\n        \"output\": \" No, K4(ZrSe5)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd3(GeRu)2\\n\",\n        \"output\": \" Yes, Nd3(GeRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li7Ca8Nb12O40\\n\",\n        \"output\": \" Yes, Li7Ca8Nb12O40 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LuP\\n\",\n        \"output\": \" No, LuP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KTaO3\\n\",\n        \"output\": \" No, KTaO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2O3\\n\",\n        \"output\": \" No, Sm2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ThMn4(CuO4)3\\n\",\n        \"output\": \" Yes, ThMn4(CuO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er2MnC4\\n\",\n        \"output\": \" Yes, Er2MnC4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KBaAsSe3\\n\",\n        \"output\": \" No, KBaAsSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CrCo2Bi\\n\",\n        \"output\": \" Yes, CrCo2Bi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn2MoSeO7\\n\",\n        \"output\": \" No, Zn2MoSeO7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs0.4K0.6P1Se6\\n\",\n        \"output\": \" No, Cs0.4K0.6P1Se6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbPr11Se16\\n\",\n        \"output\": \" Yes, YbPr11Se16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl4In3GaS8\\n\",\n        \"output\": \" No, Tl4In3GaS8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SbI3\\n\",\n        \"output\": \" No, SbI3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2TiO4\\n\",\n        \"output\": \" No, Sr2TiO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" appeal\\n\",\n        \"output\": \" appeal is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnTe\\n\",\n        \"output\": \" No, MnTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlCl\\n\",\n        \"output\": \" No, TlCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbSbS2\\n\",\n        \"output\": \" No, RbSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.92Hg0.08Te1\\n\",\n        \"output\": \" No, Zn0.92Hg0.08Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2S3\\n\",\n        \"output\": \" No, Sm2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Fe2Te3\\n\",\n        \"output\": \" No, Fe2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb5Au4\\n\",\n        \"output\": \" Yes, Yb5Au4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnSiP2\\n\",\n        \"output\": \" No, ZnSiP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlSbS2\\n\",\n        \"output\": \" No, TlSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er2C3\\n\",\n        \"output\": \" Yes, Er2C3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" course\\n\",\n        \"output\": \" course is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc14Cu14O37\\n\",\n        \"output\": \" Yes, Sc14Cu14O37 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YErRh2\\n\",\n        \"output\": \" Yes, YErRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrSbAu\\n\",\n        \"output\": \" Yes, SrSbAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3FeNi3O8\\n\",\n        \"output\": \" Yes, Li3FeNi3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScRh3C\\n\",\n        \"output\": \" Yes, ScRh3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce3Al\\n\",\n        \"output\": \" Yes, Ce3Al is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbPO4\\n\",\n        \"output\": \" Yes, YbPO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu2AgAu\\n\",\n        \"output\": \" Yes, Lu2AgAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn7O7F\\n\",\n        \"output\": \" Yes, Mn7O7F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScZnNi2\\n\",\n        \"output\": \" Yes, ScZnNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag9(PbO3)4\\n\",\n        \"output\": \" Yes, Ag9(PbO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdFeSi2\\n\",\n        \"output\": \" Yes, NdFeSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbGa\\n\",\n        \"output\": \" Yes, TbGa is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi2Te2.1Se0.9\\n\",\n        \"output\": \" No, Bi2Te2.1Se0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbRh2\\n\",\n        \"output\": \" Yes, TbRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" hot\\n\",\n        \"output\": \" hot is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te2Au\\n\",\n        \"output\": \" Yes, Te2Au is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.25Pb0.75Se1\\n\",\n        \"output\": \" No, Sn0.25Pb0.75Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" B4H2Pb6O13\\n\",\n        \"output\": \" No, B4H2Pb6O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.99Ga0.01Sb0.01Te0.99\\n\",\n        \"output\": \" No, Cd0.99Ga0.01Sb0.01Te0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FePd3\\n\",\n        \"output\": \" Yes, FePd3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnBe2Co\\n\",\n        \"output\": \" Yes, MnBe2Co is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K6Ta1.03Nb2.97S25\\n\",\n        \"output\": \" No, K6Ta1.03Nb2.97S25 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn2TeMoO7\\n\",\n        \"output\": \" No, Zn2TeMoO7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThCrB4\\n\",\n        \"output\": \" Yes, ThCrB4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hg3PS4\\n\",\n        \"output\": \" No, Hg3PS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3TlN\\n\",\n        \"output\": \" Yes, Ca3TlN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiGaPt2\\n\",\n        \"output\": \" Yes, LiGaPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KBaB5O9\\n\",\n        \"output\": \" No, KBaB5O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.05Pb0.95Se1\\n\",\n        \"output\": \" No, Sn0.05Pb0.95Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm4U4O17\\n\",\n        \"output\": \" Yes, Sm4U4O17 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu2CuO4\\n\",\n        \"output\": \" Yes, Eu2CuO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2Th(PS3)3\\n\",\n        \"output\": \" No, Cs2Th(PS3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2NiSe4\\n\",\n        \"output\": \" Yes, Ti2NiSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu2C(NO)2\\n\",\n        \"output\": \" Yes, Eu2C(NO)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaGeTe\\n\",\n        \"output\": \" No, GaGeTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaTaN2O\\n\",\n        \"output\": \" No, LaTaN2O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZnCu3P3O13\\n\",\n        \"output\": \" Yes, ZnCu3P3O13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na5Fe6(SiO3)12\\n\",\n        \"output\": \" Yes, Na5Fe6(SiO3)12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AsOsS\\n\",\n        \"output\": \" No, AsOsS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cr2HgSe4\\n\",\n        \"output\": \" Yes, Cr2HgSe4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3CrS5\\n\",\n        \"output\": \" Yes, Ba3CrS5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThBi2\\n\",\n        \"output\": \" Yes, ThBi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GdCd2\\n\",\n        \"output\": \" Yes, GdCd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdInCuSe3\\n\",\n        \"output\": \" No, CdInCuSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y3GaS6\\n\",\n        \"output\": \" No, Y3GaS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YV(BiO4)2\\n\",\n        \"output\": \" No, YV(BiO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr10Se14O\\n\",\n        \"output\": \" No, Pr10Se14O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Cd(PSe3)2\\n\",\n        \"output\": \" No, Cs2Cd(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YCdPt2\\n\",\n        \"output\": \" Yes, YCdPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2Se2O7\\n\",\n        \"output\": \" No, Ga2Se2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm3Te4\\n\",\n        \"output\": \" No, Sm3Te4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3PN\\n\",\n        \"output\": \" Yes, Ba3PN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KAg2SbS4\\n\",\n        \"output\": \" No, KAg2SbS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" quart\\n\",\n        \"output\": \" quart is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YVTeO10\\n\",\n        \"output\": \" No, YVTeO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" InSb2S4Cl\\n\",\n        \"output\": \" No, InSb2S4Cl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KHg\\n\",\n        \"output\": \" Yes, KHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsCd4In5Te12\\n\",\n        \"output\": \" No, CsCd4In5Te12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.04Te1Pb0.96\\n\",\n        \"output\": \" No, In0.04Te1Pb0.96 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce2Fe(SeO)2\\n\",\n        \"output\": \" No, Ce2Fe(SeO)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Pt\\n\",\n        \"output\": \" Yes, Bi2Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn(SbO2)2\\n\",\n        \"output\": \" No, Mn(SbO2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrNiSb\\n\",\n        \"output\": \" No, ZrNiSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr2SmTaO6\\n\",\n        \"output\": \" No, Sr2SmTaO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnInCu2\\n\",\n        \"output\": \" Yes, MnInCu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2Bi2O5\\n\",\n        \"output\": \" No, Ca2Bi2O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoAlAu2\\n\",\n        \"output\": \" Yes, HoAlAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.07In0.93Te0.07As0.93\\n\",\n        \"output\": \" No, Cd0.07In0.93Te0.07As0.93 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al0.01In0.99P1\\n\",\n        \"output\": \" No, Al0.01In0.99P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2ZnReO6\\n\",\n        \"output\": \" Yes, Sr2ZnReO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiZr2Os\\n\",\n        \"output\": \" Yes, LiZr2Os is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaNa2GeS4\\n\",\n        \"output\": \" No, BaNa2GeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs4Cu3Bi9S17\\n\",\n        \"output\": \" No, Cs4Cu3Bi9S17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" meeting\\n\",\n        \"output\": \" meeting is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y(SiRu)2\\n\",\n        \"output\": \" Yes, Y(SiRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaCdAsS3\\n\",\n        \"output\": \" No, NaCdAsS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KUCuSe3\\n\",\n        \"output\": \" Yes, KUCuSe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd8B5O15F\\n\",\n        \"output\": \" No, Cd8B5O15F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La8Mn7O24\\n\",\n        \"output\": \" Yes, La8Mn7O24 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga0.005Te1Pb0.995\\n\",\n        \"output\": \" No, Ga0.005Te1Pb0.995 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Si0.1Ge0.9\\n\",\n        \"output\": \" No, Si0.1Ge0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgCl\\n\",\n        \"output\": \" No, AgCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm(CuTe)3\\n\",\n        \"output\": \" No, Sm(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.86Hg0.14Te1\\n\",\n        \"output\": \" No, Zn0.86Hg0.14Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2ZnNi2\\n\",\n        \"output\": \" Yes, Ce2ZnNi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbGeB3O7\\n\",\n        \"output\": \" No, RbGeB3O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb2InPd2\\n\",\n        \"output\": \" Yes, Yb2InPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy(CuTe)3\\n\",\n        \"output\": \" No, Dy(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiSn(PO3)4\\n\",\n        \"output\": \" Yes, LiSn(PO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca(Ni2O3)2\\n\",\n        \"output\": \" Yes, Ca(Ni2O3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc3C4\\n\",\n        \"output\": \" Yes, Sc3C4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlCu7O12\\n\",\n        \"output\": \" Yes, AlCu7O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdBRh3\\n\",\n        \"output\": \" Yes, NdBRh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti(Bi3O5)4\\n\",\n        \"output\": \" No, Ti(Bi3O5)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbInGeS4\\n\",\n        \"output\": \" No, RbInGeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2(FeO2)5\\n\",\n        \"output\": \" Yes, Li2(FeO2)5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg(SnO2)4\\n\",\n        \"output\": \" Yes, Mg(SnO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ni3Ge\\n\",\n        \"output\": \" Yes, Ni3Ge is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K3Cr2(PS4)3\\n\",\n        \"output\": \" No, K3Cr2(PS4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2CuAs3O\\n\",\n        \"output\": \" Yes, Sm2CuAs3O is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba23Ga8(SbS19)2\\n\",\n        \"output\": \" No, Ba23Ga8(SbS19)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" UFe5Si3\\n\",\n        \"output\": \" Yes, UFe5Si3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyS2\\n\",\n        \"output\": \" Yes, DyS2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" IrSeS\\n\",\n        \"output\": \" No, IrSeS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NbCrN\\n\",\n        \"output\": \" Yes, NbCrN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi2Te0.45Se2.55\\n\",\n        \"output\": \" No, Bi2Te0.45Se2.55 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Hg(PSe3)2\\n\",\n        \"output\": \" No, K2Hg(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlCr5Se7S\\n\",\n        \"output\": \" No, TlCr5Se7S is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PH6NO4\\n\",\n        \"output\": \" No, PH6NO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.2Ga0.8Sb0.8Te0.2\\n\",\n        \"output\": \" No, Zn0.2Ga0.8Sb0.8Te0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" viscose\\n\",\n        \"output\": \" viscose is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsCeCdSe3\\n\",\n        \"output\": \" No, CsCeCdSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaSm(PS3)2\\n\",\n        \"output\": \" No, NaSm(PS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiTaRh2\\n\",\n        \"output\": \" Yes, LiTaRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrIn2Rh\\n\",\n        \"output\": \" Yes, SrIn2Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li17Nb20O60\\n\",\n        \"output\": \" Yes, Li17Nb20O60 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3Mo4O16F\\n\",\n        \"output\": \" No, La3Mo4O16F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm2ZnHg\\n\",\n        \"output\": \" Yes, Tm2ZnHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeOs2\\n\",\n        \"output\": \" Yes, CeOs2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiSiB6\\n\",\n        \"output\": \" No, LiSiB6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho(NiB)2\\n\",\n        \"output\": \" Yes, Ho(NiB)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg3(Ni10B3)2\\n\",\n        \"output\": \" Yes, Mg3(Ni10B3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu2O\\n\",\n        \"output\": \" No, Cu2O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy12Co7\\n\",\n        \"output\": \" Yes, Dy12Co7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaFe3\\n\",\n        \"output\": \" Yes, GaFe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho4Ga16Co3\\n\",\n        \"output\": \" Yes, Ho4Ga16Co3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce(MnSi)2\\n\",\n        \"output\": \" Yes, Ce(MnSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg3As2\\n\",\n        \"output\": \" No, Mg3As2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.109Ge0.891\\n\",\n        \"output\": \" No, Si0.109Ge0.891 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al3Tc\\n\",\n        \"output\": \" Yes, Al3Tc is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.8Hg0.2Se1\\n\",\n        \"output\": \" No, Cd0.8Hg0.2Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs3Nb2AsSe11\\n\",\n        \"output\": \" No, Cs3Nb2AsSe11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca6Cu2Sn7\\n\",\n        \"output\": \" Yes, Ca6Cu2Sn7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2Sn3(SbS5)2\\n\",\n        \"output\": \" No, Rb2Sn3(SbS5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2IrPd\\n\",\n        \"output\": \" Yes, Sm2IrPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrSbPt\\n\",\n        \"output\": \" Yes, PrSbPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K3Bi2I9\\n\",\n        \"output\": \" No, K3Bi2I9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgCu2GeS4\\n\",\n        \"output\": \" No, MgCu2GeS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaCuSbSe3\\n\",\n        \"output\": \" No, BaCuSbSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" UNiSn\\n\",\n        \"output\": \" Yes, UNiSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2TeS3\\n\",\n        \"output\": \" No, Na2TeS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TmCdAg2\\n\",\n        \"output\": \" Yes, TmCdAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrPb3Br8\\n\",\n        \"output\": \" No, SrPb3Br8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" B5Mo2\\n\",\n        \"output\": \" Yes, B5Mo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KEuS2\\n\",\n        \"output\": \" Yes, KEuS2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl3AsSe3\\n\",\n        \"output\": \" No, Tl3AsSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbTe\\n\",\n        \"output\": \" Yes, TbTe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaSbTe2\\n\",\n        \"output\": \" No, NaSbTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeGaO3\\n\",\n        \"output\": \" Yes, CeGaO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ThO2\\n\",\n        \"output\": \" No, ThO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KTeP2\\n\",\n        \"output\": \" No, KTeP2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn2SnN2\\n\",\n        \"output\": \" Yes, Zn2SnN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuC2\\n\",\n        \"output\": \" Yes, LuC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2V4(TeO6)3\\n\",\n        \"output\": \" No, Ba2V4(TeO6)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg3Rh\\n\",\n        \"output\": \" Yes, Mg3Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TiFe2As\\n\",\n        \"output\": \" Yes, TiFe2As is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pb1Se0.5S0.5\\n\",\n        \"output\": \" No, Pb1Se0.5S0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc3(MnGa3)2\\n\",\n        \"output\": \" Yes, Sc3(MnGa3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2Pt(IO3)6\\n\",\n        \"output\": \" No, Rb2Pt(IO3)6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Hg3(GeS4)2\\n\",\n        \"output\": \" No, Rb2Hg3(GeS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsNi2F6\\n\",\n        \"output\": \" Yes, CsNi2F6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaAgO2\\n\",\n        \"output\": \" No, GaAgO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThPSe\\n\",\n        \"output\": \" Yes, ThPSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CrIrO4\\n\",\n        \"output\": \" Yes, CrIrO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2PdAu\\n\",\n        \"output\": \" Yes, Mg2PdAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li6FeNi9O20\\n\",\n        \"output\": \" Yes, Li6FeNi9O20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuBiPbSe3\\n\",\n        \"output\": \" No, CuBiPbSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg3Sb2\\n\",\n        \"output\": \" No, Mg3Sb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn(PbO2)2\\n\",\n        \"output\": \" No, Mn(PbO2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2FeSnS4\\n\",\n        \"output\": \" No, Li2FeSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3Gd2(PS4)4\\n\",\n        \"output\": \" No, Ba3Gd2(PS4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb6PbSe10\\n\",\n        \"output\": \" Yes, Tb6PbSe10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiGaTe2\\n\",\n        \"output\": \" No, LiGaTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2Ag3Sb3S7\\n\",\n        \"output\": \" No, K2Ag3Sb3S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3FeS3\\n\",\n        \"output\": \" Yes, Li3FeS3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbInSnS4\\n\",\n        \"output\": \" No, RbInSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Co4O7F\\n\",\n        \"output\": \" Yes, Li2Co4O7F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2TlZn\\n\",\n        \"output\": \" Yes, Sm2TlZn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HoCdCu4\\n\",\n        \"output\": \" Yes, HoCdCu4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er(CuTe)3\\n\",\n        \"output\": \" No, Er(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi2Te2.97Se0.03\\n\",\n        \"output\": \" No, Bi2Te2.97Se0.03 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TeO2\\n\",\n        \"output\": \" No, TeO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho3Ni19B10\\n\",\n        \"output\": \" Yes, Ho3Ni19B10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb(GaSe2)2\\n\",\n        \"output\": \" No, Yb(GaSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnNbO4\\n\",\n        \"output\": \" Yes, MnNbO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrAl3Ni2\\n\",\n        \"output\": \" Yes, PrAl3Ni2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbCu2SbS3\\n\",\n        \"output\": \" No, RbCu2SbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Lu(SiOs)2\\n\",\n        \"output\": \" Yes, Lu(SiOs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb4Ga4Si19\\n\",\n        \"output\": \" No, Rb4Ga4Si19 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3NaIr2O9\\n\",\n        \"output\": \" Yes, Ba3NaIr2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr5Bi3\\n\",\n        \"output\": \" Yes, Sr5Bi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Lu2Fe2Si2C\\n\",\n        \"output\": \" Yes, Lu2Fe2Si2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsMn4Ga5Te12\\n\",\n        \"output\": \" No, CsMn4Ga5Te12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaMn4ZnO8\\n\",\n        \"output\": \" Yes, BaMn4ZnO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GeO2\\n\",\n        \"output\": \" No, GeO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ni2Ge\\n\",\n        \"output\": \" Yes, Ni2Ge is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl8Os8O27\\n\",\n        \"output\": \" Yes, Tl8Os8O27 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmMg3\\n\",\n        \"output\": \" Yes, SmMg3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La10Mn9O30\\n\",\n        \"output\": \" Yes, La10Mn9O30 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbPr2CuS5\\n\",\n        \"output\": \" No, YbPr2CuS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbSBr\\n\",\n        \"output\": \" No, SbSBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiNbO3\\n\",\n        \"output\": \" No, LiNbO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy2TlCd\\n\",\n        \"output\": \" Yes, Dy2TlCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2MnFe\\n\",\n        \"output\": \" Yes, Ti2MnFe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGa4Se7\\n\",\n        \"output\": \" No, BaGa4Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" sagittarius\\n\",\n        \"output\": \" sagittarius is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ErMg2\\n\",\n        \"output\": \" Yes, ErMg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiMo3O8\\n\",\n        \"output\": \" Yes, LiMo3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SnPbS3\\n\",\n        \"output\": \" No, SnPbS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb(AlGa)2\\n\",\n        \"output\": \" Yes, Yb(AlGa)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InBi2S4Cl\\n\",\n        \"output\": \" No, InBi2S4Cl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2Se3\\n\",\n        \"output\": \" No, La2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AsAu3\\n\",\n        \"output\": \" Yes, AsAu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3In2(PO4)4\\n\",\n        \"output\": \" No, Ba3In2(PO4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pb3O4\\n\",\n        \"output\": \" No, Pb3O4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1As0.8P0.2\\n\",\n        \"output\": \" No, Ga1As0.8P0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AgI\\n\",\n        \"output\": \" No, AgI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rh0.67S2\\n\",\n        \"output\": \" No, Rh0.67S2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Mo2Se2O11\\n\",\n        \"output\": \" No, Na2Mo2Se2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er(Al10Cr)2\\n\",\n        \"output\": \" Yes, Er(Al10Cr)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" respect\\n\",\n        \"output\": \" respect is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K4C2O3\\n\",\n        \"output\": \" Yes, K4C2O3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li6Mn5CoO12\\n\",\n        \"output\": \" Yes, Li6Mn5CoO12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TePb3Cl4O3\\n\",\n        \"output\": \" No, TePb3Cl4O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbNb3(TeO6)2\\n\",\n        \"output\": \" No, RbNb3(TeO6)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr(Ni2P)2\\n\",\n        \"output\": \" Yes, Zr(Ni2P)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce(CoAs)2\\n\",\n        \"output\": \" Yes, Ce(CoAs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hg3Sb\\n\",\n        \"output\": \" Yes, Hg3Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SnS2\\n\",\n        \"output\": \" No, SnS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PmHgAu2\\n\",\n        \"output\": \" Yes, PmHgAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfO2\\n\",\n        \"output\": \" No, HfO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KAg2PS4\\n\",\n        \"output\": \" No, KAg2PS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" jogging\\n\",\n        \"output\": \" jogging is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZnAgF5\\n\",\n        \"output\": \" Yes, ZnAgF5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm3OsO7\\n\",\n        \"output\": \" Yes, Sm3OsO7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd0.05In0.95Te0.05As0.95\\n\",\n        \"output\": \" No, Cd0.05In0.95Te0.05As0.95 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnCoSi\\n\",\n        \"output\": \" Yes, MnCoSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb4Ti3S14\\n\",\n        \"output\": \" No, Rb4Ti3S14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbSe2\\n\",\n        \"output\": \" Yes, TbSe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CePrO2\\n\",\n        \"output\": \" Yes, CePrO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbHgSbTe3\\n\",\n        \"output\": \" No, RbHgSbTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm(SiAg)2\\n\",\n        \"output\": \" Yes, Sm(SiAg)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2Ga8GeS16\\n\",\n        \"output\": \" No, Ba2Ga8GeS16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdMoO4F\\n\",\n        \"output\": \" No, NdMoO4F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr2Ge2Se7\\n\",\n        \"output\": \" No, Pr2Ge2Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" VCu3S4\\n\",\n        \"output\": \" No, VCu3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr7Mn8O24\\n\",\n        \"output\": \" Yes, Pr7Mn8O24 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SiTe2\\n\",\n        \"output\": \" No, SiTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InPt3C\\n\",\n        \"output\": \" Yes, InPt3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3In1Ge0.5S7\\n\",\n        \"output\": \" No, La3In1Ge0.5S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsCd4Ga5Te12\\n\",\n        \"output\": \" No, CsCd4Ga5Te12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb(SiRh)2\\n\",\n        \"output\": \" Yes, Yb(SiRh)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Yb(SiAg)2\\n\",\n        \"output\": \" Yes, Yb(SiAg)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BeGaO3\\n\",\n        \"output\": \" Yes, BeGaO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn1Se0.01S0.99\\n\",\n        \"output\": \" No, Sn1Se0.01S0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.06Te1Pb0.94\\n\",\n        \"output\": \" No, Sn0.06Te1Pb0.94 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb2Sn\\n\",\n        \"output\": \" Yes, Yb2Sn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Te2Ru\\n\",\n        \"output\": \" No, Te2Ru is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoCo3\\n\",\n        \"output\": \" Yes, HoCo3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SrIn2(GeIr)4\\n\",\n        \"output\": \" No, SrIn2(GeIr)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaTl3\\n\",\n        \"output\": \" Yes, BaTl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2DyGaSe5\\n\",\n        \"output\": \" No, Ba2DyGaSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr3I\\n\",\n        \"output\": \" Yes, Pr3I is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MnSnRu2\\n\",\n        \"output\": \" Yes, MnSnRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr5V3O12F\\n\",\n        \"output\": \" No, Sr5V3O12F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" DyYAg2\\n\",\n        \"output\": \" Yes, DyYAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd(CuSe)3\\n\",\n        \"output\": \" No, Gd(CuSe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" year\\n\",\n        \"output\": \" year is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nb6Co7\\n\",\n        \"output\": \" Yes, Nb6Co7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaCl\\n\",\n        \"output\": \" No, NaCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LuPt3\\n\",\n        \"output\": \" Yes, LuPt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsRb2Sb\\n\",\n        \"output\": \" No, CsRb2Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaS\\n\",\n        \"output\": \" No, CaS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaAg\\n\",\n        \"output\": \" Yes, BaAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr2Te3\\n\",\n        \"output\": \" No, Pr2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ca2Sn2F3\\n\",\n        \"output\": \" Yes, Ca2Sn2F3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ta3B4\\n\",\n        \"output\": \" Yes, Ta3B4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsYbCoSe3\\n\",\n        \"output\": \" No, CsYbCoSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaPdSe6\\n\",\n        \"output\": \" No, BaPdSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BPb2ClO3\\n\",\n        \"output\": \" No, BPb2ClO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.99Ga0.01As0.99P0.01\\n\",\n        \"output\": \" No, In0.99Ga0.01As0.99P0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ti4NiBi2\\n\",\n        \"output\": \" Yes, Ti4NiBi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb3Ta2AsS11\\n\",\n        \"output\": \" No, Rb3Ta2AsS11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3Cd4(TeO5)3\\n\",\n        \"output\": \" No, V3Cd4(TeO5)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoN\\n\",\n        \"output\": \" No, HoN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BaLi4\\n\",\n        \"output\": \" Yes, BaLi4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho3AlC\\n\",\n        \"output\": \" Yes, Ho3AlC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U(BH4)4\\n\",\n        \"output\": \" Yes, U(BH4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc5Bi3\\n\",\n        \"output\": \" Yes, Sc5Bi3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsGdZnTe3\\n\",\n        \"output\": \" No, CsGdZnTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyAgGe\\n\",\n        \"output\": \" Yes, DyAgGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KCu2BiS3\\n\",\n        \"output\": \" No, KCu2BiS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrPbO3\\n\",\n        \"output\": \" No, SrPbO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb(CuSe)3\\n\",\n        \"output\": \" No, Tb(CuSe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmNiC2\\n\",\n        \"output\": \" Yes, SmNiC2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LuU2S3O2\\n\",\n        \"output\": \" Yes, LuU2S3O2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca11Ga7\\n\",\n        \"output\": \" Yes, Ca11Ga7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" WSe2\\n\",\n        \"output\": \" No, WSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmIn3\\n\",\n        \"output\": \" Yes, TmIn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuTiClO3\\n\",\n        \"output\": \" Yes, EuTiClO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2Cd(IBr)2\\n\",\n        \"output\": \" No, Rb2Cd(IBr)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.05Sb0.95Te0.15\\n\",\n        \"output\": \" No, Ga1.05Sb0.95Te0.15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(InS2)2\\n\",\n        \"output\": \" No, Eu(InS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba7Ru4Br2O15\\n\",\n        \"output\": \" Yes, Ba7Ru4Br2O15 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr(CeSe2)2\\n\",\n        \"output\": \" Yes, Sr(CeSe2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" vacuum\\n\",\n        \"output\": \" vacuum is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiPm2Al\\n\",\n        \"output\": \" Yes, LiPm2Al is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgN3\\n\",\n        \"output\": \" No, AgN3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nb3VS6\\n\",\n        \"output\": \" Yes, Nb3VS6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti9O10\\n\",\n        \"output\": \" Yes, Ti9O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm4In21Pd10\\n\",\n        \"output\": \" Yes, Sm4In21Pd10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl2Te3\\n\",\n        \"output\": \" No, Tl2Te3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdAuO2\\n\",\n        \"output\": \" Yes, CdAuO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na10(Ga2Sn)3\\n\",\n        \"output\": \" Yes, Na10(Ga2Sn)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li13Nb14ZnO42\\n\",\n        \"output\": \" Yes, Li13Nb14ZnO42 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm2AlCd\\n\",\n        \"output\": \" Yes, Sm2AlCd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn2S\\n\",\n        \"output\": \" No, Sn2S is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4(FeO2)9\\n\",\n        \"output\": \" Yes, Li4(FeO2)9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Te0.3Se2.7\\n\",\n        \"output\": \" No, Bi2Te0.3Se2.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PmSbRh2\\n\",\n        \"output\": \" Yes, PmSbRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HoSiRu2C\\n\",\n        \"output\": \" Yes, HoSiRu2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeHSe\\n\",\n        \"output\": \" Yes, CeHSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiS3\\n\",\n        \"output\": \" No, TiS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sb2S3\\n\",\n        \"output\": \" No, Sb2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn5(BIr3)2\\n\",\n        \"output\": \" Yes, Sn5(BIr3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YSi2\\n\",\n        \"output\": \" Yes, YSi2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl2TeI6\\n\",\n        \"output\": \" No, Tl2TeI6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaAu5\\n\",\n        \"output\": \" Yes, CaAu5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YAs\\n\",\n        \"output\": \" Yes, YAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScTiNbO6\\n\",\n        \"output\": \" No, ScTiNbO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca2CuWO6\\n\",\n        \"output\": \" Yes, Ca2CuWO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hg3C\\n\",\n        \"output\": \" Yes, Hg3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Si0.9Ge0.1\\n\",\n        \"output\": \" No, Si0.9Ge0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd(CuS)3\\n\",\n        \"output\": \" No, Gd(CuS)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdPt\\n\",\n        \"output\": \" Yes, CdPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaNa2SnSe4\\n\",\n        \"output\": \" No, BaNa2SnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsCd4Ga5Se12\\n\",\n        \"output\": \" No, CsCd4Ga5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In3Sb\\n\",\n        \"output\": \" Yes, In3Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sm(ErSe2)3\\n\",\n        \"output\": \" No, Sm(ErSe2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ScTiO3\\n\",\n        \"output\": \" Yes, ScTiO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NiO\\n\",\n        \"output\": \" No, NiO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2Sc3\\n\",\n        \"output\": \" No, Sm2Sc3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdAu3\\n\",\n        \"output\": \" Yes, NdAu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbSm2CuS5\\n\",\n        \"output\": \" No, YbSm2CuS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn0.1Te1Pb0.9\\n\",\n        \"output\": \" No, Mn0.1Te1Pb0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu2TeO2\\n\",\n        \"output\": \" Yes, Eu2TeO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiSCl\\n\",\n        \"output\": \" No, BiSCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2ZnGe3Te8\\n\",\n        \"output\": \" No, Cs2ZnGe3Te8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2SmCu3O7\\n\",\n        \"output\": \" Yes, Ba2SmCu3O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LaCd2\\n\",\n        \"output\": \" Yes, LaCd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrIn\\n\",\n        \"output\": \" Yes, PrIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho(MnSn)6\\n\",\n        \"output\": \" Yes, Ho(MnSn)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" InSb\\n\",\n        \"output\": \" No, InSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li3Mn4O8\\n\",\n        \"output\": \" Yes, Li3Mn4O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3ThSe7\\n\",\n        \"output\": \" No, Ba3ThSe7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba4Ga5AgS12\\n\",\n        \"output\": \" No, Ba4Ga5AgS12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In11Cu9Se20\\n\",\n        \"output\": \" Yes, In11Cu9Se20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgZn2\\n\",\n        \"output\": \" Yes, MgZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1Sb0.01As0.99\\n\",\n        \"output\": \" No, Ga1Sb0.01As0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TeSe\\n\",\n        \"output\": \" No, TeSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YH2NO5\\n\",\n        \"output\": \" No, YH2NO5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd5Ga2(Te3S)2\\n\",\n        \"output\": \" No, Cd5Ga2(Te3S)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" VFeSb\\n\",\n        \"output\": \" No, VFeSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsAg2AsS3\\n\",\n        \"output\": \" No, CsAg2AsS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.001Te1Pb0.999\\n\",\n        \"output\": \" No, In0.001Te1Pb0.999 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1.99Cu0.01Se2.99\\n\",\n        \"output\": \" No, In1.99Cu0.01Se2.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaInSnS4\\n\",\n        \"output\": \" No, NaInSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ReOsRu\\n\",\n        \"output\": \" Yes, ReOsRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SnSe2\\n\",\n        \"output\": \" No, SnSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" decrease\\n\",\n        \"output\": \" decrease is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlCoBi\\n\",\n        \"output\": \" Yes, TlCoBi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbBr3\\n\",\n        \"output\": \" Yes, RbBr3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2B6O9F2\\n\",\n        \"output\": \" No, Na2B6O9F2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Te\\n\",\n        \"output\": \" No, Na2Te is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Mn3NiO8\\n\",\n        \"output\": \" Yes, Li3Mn3NiO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd1.05Sc0.95Se3\\n\",\n        \"output\": \" No, Gd1.05Sc0.95Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag5IO6\\n\",\n        \"output\": \" No, Ag5IO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" AgBi(PS3)2\\n\",\n        \"output\": \" No, AgBi(PS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrS3\\n\",\n        \"output\": \" No, ZrS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsYCdSe3\\n\",\n        \"output\": \" No, CsYCdSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.17Te1Pb0.83\\n\",\n        \"output\": \" No, Sn0.17Te1Pb0.83 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbAgF3\\n\",\n        \"output\": \" Yes, RbAgF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li5(BiO3)4\\n\",\n        \"output\": \" Yes, Li5(BiO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr3Ti2O7\\n\",\n        \"output\": \" No, Sr3Ti2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuN\\n\",\n        \"output\": \" No, EuN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tb3Ge5\\n\",\n        \"output\": \" Yes, Tb3Ge5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BSb\\n\",\n        \"output\": \" No, BSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2BiSbO6\\n\",\n        \"output\": \" Yes, Ba2BiSbO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaHgS2\\n\",\n        \"output\": \" No, BaHgS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi1Sb0.15\\n\",\n        \"output\": \" No, Bi1Sb0.15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2SCl6F\\n\",\n        \"output\": \" Yes, Cs2SCl6F is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy5Pb3\\n\",\n        \"output\": \" Yes, Dy5Pb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HgS\\n\",\n        \"output\": \" No, HgS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ag2SnSe3\\n\",\n        \"output\": \" No, Ag2SnSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiIO3F2\\n\",\n        \"output\": \" No, BiIO3F2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" child\\n\",\n        \"output\": \" child is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La(In2Au)2\\n\",\n        \"output\": \" Yes, La(In2Au)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Bi0.4Te0.6Pb0.8Se0.8\\n\",\n        \"output\": \" No, Bi0.4Te0.6Pb0.8Se0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2TiIrO6\\n\",\n        \"output\": \" Yes, Mg2TiIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li8GeN4\\n\",\n        \"output\": \" No, Li8GeN4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn3As2\\n\",\n        \"output\": \" No, Zn3As2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm3Al0.33Si1S7\\n\",\n        \"output\": \" No, Sm3Al0.33Si1S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsCd4In5Se12\\n\",\n        \"output\": \" No, CsCd4In5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr2Co2O5\\n\",\n        \"output\": \" Yes, Sr2Co2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sc11(AlGe4)2\\n\",\n        \"output\": \" Yes, Sc11(AlGe4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy6FeTe2\\n\",\n        \"output\": \" Yes, Dy6FeTe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" B3Pb10Br3O13\\n\",\n        \"output\": \" No, B3Pb10Br3O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U3Se4\\n\",\n        \"output\": \" Yes, U3Se4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbGeRh\\n\",\n        \"output\": \" Yes, YbGeRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdGeAs2\\n\",\n        \"output\": \" No, CdGeAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb3Li4(BO2)7\\n\",\n        \"output\": \" No, Rb3Li4(BO2)7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AsS\\n\",\n        \"output\": \" No, AsS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl2InGaSe4\\n\",\n        \"output\": \" No, Tl2InGaSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PSe\\n\",\n        \"output\": \" No, PSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" volleyball\\n\",\n        \"output\": \" volleyball is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y2Ge2O7\\n\",\n        \"output\": \" Yes, Y2Ge2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu3(P2O7)2\\n\",\n        \"output\": \" Yes, Cu3(P2O7)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiGaIr2\\n\",\n        \"output\": \" Yes, TiGaIr2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K4Ag9(SbS3)4\\n\",\n        \"output\": \" No, K4Ag9(SbS3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiMgN\\n\",\n        \"output\": \" No, LiMgN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TlInSe2\\n\",\n        \"output\": \" No, TlInSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KGaSe2\\n\",\n        \"output\": \" No, KGaSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Er3Al3NiGe2\\n\",\n        \"output\": \" Yes, Er3Al3NiGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" geese\\n\",\n        \"output\": \" geese is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb2Ru\\n\",\n        \"output\": \" No, Sb2Ru is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn2In2S5\\n\",\n        \"output\": \" No, Zn2In2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaCdO3\\n\",\n        \"output\": \" Yes, NaCdO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca(BiO2)2\\n\",\n        \"output\": \" No, Ca(BiO2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbSn2Pd\\n\",\n        \"output\": \" Yes, YbSn2Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2TaInO6\\n\",\n        \"output\": \" No, Ba2TaInO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ErZn12\\n\",\n        \"output\": \" Yes, ErZn12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd0.23Hg0.77Te1\\n\",\n        \"output\": \" No, Cd0.23Hg0.77Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag3RuO4\\n\",\n        \"output\": \" Yes, Ag3RuO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgO\\n\",\n        \"output\": \" No, AgO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(TmSe2)2\\n\",\n        \"output\": \" No, Eu(TmSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiTmSn\\n\",\n        \"output\": \" Yes, LiTmSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2PS5\\n\",\n        \"output\": \" No, Rb2PS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CoN\\n\",\n        \"output\": \" Yes, CoN is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaZnAu2\\n\",\n        \"output\": \" Yes, LaZnAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiAuCl\\n\",\n        \"output\": \" Yes, TiAuCl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3CaRu2O9\\n\",\n        \"output\": \" Yes, Ba3CaRu2O9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LaF3\\n\",\n        \"output\": \" No, LaF3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YBi\\n\",\n        \"output\": \" Yes, YBi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ru3Cl\\n\",\n        \"output\": \" Yes, Ru3Cl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ThAl3\\n\",\n        \"output\": \" Yes, ThAl3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbGa2Pd\\n\",\n        \"output\": \" Yes, YbGa2Pd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb3ReO7\\n\",\n        \"output\": \" Yes, Tb3ReO7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" inventory\\n\",\n        \"output\": \" inventory is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmB66\\n\",\n        \"output\": \" No, SmB66 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na19Zr11S30\\n\",\n        \"output\": \" Yes, Na19Zr11S30 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" PtS2\\n\",\n        \"output\": \" No, PtS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbCd4Ga5S12\\n\",\n        \"output\": \" No, RbCd4Ga5S12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaBiClO2\\n\",\n        \"output\": \" No, BaBiClO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1Sb0.7As0.3\\n\",\n        \"output\": \" No, In1Sb0.7As0.3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4CrO5\\n\",\n        \"output\": \" Yes, Li4CrO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In4Bi3S10\\n\",\n        \"output\": \" No, In4Bi3S10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd3AgPS6\\n\",\n        \"output\": \" No, Cd3AgPS6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdF2\\n\",\n        \"output\": \" No, CdF2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Th2GeSe2\\n\",\n        \"output\": \" No, Th2GeSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaBClF4\\n\",\n        \"output\": \" No, BaBClF4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs(MoO3)3\\n\",\n        \"output\": \" Yes, Cs(MoO3)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca3In\\n\",\n        \"output\": \" Yes, Ca3In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaSb\\n\",\n        \"output\": \" No, LaSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NaBiSe2\\n\",\n        \"output\": \" No, NaBiSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U(CuP)2\\n\",\n        \"output\": \" Yes, U(CuP)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zn0.75Hg0.25Te1\\n\",\n        \"output\": \" No, Zn0.75Hg0.25Te1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaEu2O3\\n\",\n        \"output\": \" Yes, CaEu2O3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ferry\\n\",\n        \"output\": \" ferry is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.3Pb0.7Se1\\n\",\n        \"output\": \" No, Ge0.3Pb0.7Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb(AlGe)2\\n\",\n        \"output\": \" Yes, Yb(AlGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GaAs\\n\",\n        \"output\": \" No, GaAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La(FeAs3)4\\n\",\n        \"output\": \" Yes, La(FeAs3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdSbPd\\n\",\n        \"output\": \" Yes, GdSbPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" DyNiSn\\n\",\n        \"output\": \" Yes, DyNiSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" cardigan\\n\",\n        \"output\": \" cardigan is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" cucumber\\n\",\n        \"output\": \" cucumber is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al0.4Cd0.6Sb0.4Te0.6\\n\",\n        \"output\": \" No, Al0.4Cd0.6Sb0.4Te0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg3(B25C4)2\\n\",\n        \"output\": \" No, Mg3(B25C4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GaTe\\n\",\n        \"output\": \" No, GaTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La2MnNiO6\\n\",\n        \"output\": \" No, La2MnNiO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.4Ge0.6\\n\",\n        \"output\": \" No, Si0.4Ge0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2ZnTe3\\n\",\n        \"output\": \" No, Ba2ZnTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" EuSe\\n\",\n        \"output\": \" No, EuSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrTiF6\\n\",\n        \"output\": \" Yes, ZrTiF6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4Co2Ni3O10\\n\",\n        \"output\": \" Yes, Li4Co2Ni3O10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeCdAu2\\n\",\n        \"output\": \" Yes, CeCdAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ge(Bi3O5)4\\n\",\n        \"output\": \" No, Ge(Bi3O5)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs2Cd2Bi2S5\\n\",\n        \"output\": \" No, Cs2Cd2Bi2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaMnSn\\n\",\n        \"output\": \" Yes, CaMnSn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbZn4In5Se12\\n\",\n        \"output\": \" No, RbZn4In5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" P2Rh\\n\",\n        \"output\": \" No, P2Rh is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.99Cu0.01Se2.99\\n\",\n        \"output\": \" No, Ga1.99Cu0.01Se2.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PbO2\\n\",\n        \"output\": \" No, PbO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr3Se3ClO8\\n\",\n        \"output\": \" No, Sr3Se3ClO8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd(GaS2)2\\n\",\n        \"output\": \" No, Cd(GaS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TeMoSe\\n\",\n        \"output\": \" Yes, TeMoSe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuGaRh2\\n\",\n        \"output\": \" Yes, LuGaRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" caravan\\n\",\n        \"output\": \" caravan is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(LuSe2)2\\n\",\n        \"output\": \" No, Eu(LuSe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YSiRu\\n\",\n        \"output\": \" Yes, YSiRu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsHo9(Cd2Se9)2\\n\",\n        \"output\": \" No, CsHo9(Cd2Se9)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce2Ge2Se7\\n\",\n        \"output\": \" No, Ce2Ge2Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UPt3\\n\",\n        \"output\": \" Yes, UPt3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MgPt5\\n\",\n        \"output\": \" Yes, MgPt5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na4Mg(SiSe3)2\\n\",\n        \"output\": \" No, Na4Mg(SiSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U2Cr30P19\\n\",\n        \"output\": \" Yes, U2Cr30P19 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Th(GePd)2\\n\",\n        \"output\": \" Yes, Th(GePd)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr(YbS2)2\\n\",\n        \"output\": \" Yes, Sr(YbS2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ag9Ge2IO8\\n\",\n        \"output\": \" Yes, Ag9Ge2IO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KCu4AsS4\\n\",\n        \"output\": \" No, KCu4AsS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm2Ru2O7\\n\",\n        \"output\": \" Yes, Tm2Ru2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NbAg2(PS4)2\\n\",\n        \"output\": \" No, NbAg2(PS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuScRu2\\n\",\n        \"output\": \" Yes, LuScRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(InTe2)2\\n\",\n        \"output\": \" No, Eu(InTe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PrLuSe3\\n\",\n        \"output\": \" No, PrLuSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti2C\\n\",\n        \"output\": \" Yes, Ti2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd(PS2)2\\n\",\n        \"output\": \" No, Cd(PS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca10Ge16(B2O17)3\\n\",\n        \"output\": \" No, Ca10Ge16(B2O17)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GaAgGe3Se8\\n\",\n        \"output\": \" No, GaAgGe3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y2U3O11\\n\",\n        \"output\": \" Yes, Y2U3O11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeScO3\\n\",\n        \"output\": \" No, CeScO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaO\\n\",\n        \"output\": \" No, CaO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaF\\n\",\n        \"output\": \" No, NaF is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.99Ga0.01P0.01S0.99\\n\",\n        \"output\": \" No, Zn0.99Ga0.01P0.01S0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdCu2GeSe4\\n\",\n        \"output\": \" No, CdCu2GeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb3Ni13B2\\n\",\n        \"output\": \" Yes, Tb3Ni13B2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Ni2SbO6\\n\",\n        \"output\": \" Yes, Li2Ni2SbO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2Si5Rh3\\n\",\n        \"output\": \" Yes, La2Si5Rh3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3Si\\n\",\n        \"output\": \" Yes, V3Si is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1.7Cu0.3S2.7\\n\",\n        \"output\": \" No, Ga1.7Cu0.3S2.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Yb3Al5O12\\n\",\n        \"output\": \" Yes, Yb3Al5O12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbGa3\\n\",\n        \"output\": \" Yes, TbGa3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" ZrHg4(PCl3)2\\n\",\n        \"output\": \" No, ZrHg4(PCl3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl6Cu(TeO5)2\\n\",\n        \"output\": \" No, Tl6Cu(TeO5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KSm2CuS4\\n\",\n        \"output\": \" No, KSm2CuS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LuScZn2\\n\",\n        \"output\": \" Yes, LuScZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te2Mo(WS2)3\\n\",\n        \"output\": \" Yes, Te2Mo(WS2)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.4Ga0.6As0.6P0.4\\n\",\n        \"output\": \" No, In0.4Ga0.6As0.6P0.4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce15B8N25\\n\",\n        \"output\": \" No, Ce15B8N25 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pr5In11Ni6\\n\",\n        \"output\": \" Yes, Pr5In11Ni6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuN3\\n\",\n        \"output\": \" No, CuN3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NbGaCo2\\n\",\n        \"output\": \" Yes, NbGaCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd10Se14O\\n\",\n        \"output\": \" No, Nd10Se14O is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ti2TcPd\\n\",\n        \"output\": \" Yes, Ti2TcPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LaP3\\n\",\n        \"output\": \" Yes, LaP3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pb17(Cl9O4)2\\n\",\n        \"output\": \" No, Pb17(Cl9O4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoMgZn2\\n\",\n        \"output\": \" Yes, HoMgZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na3MoClO4\\n\",\n        \"output\": \" No, Na3MoClO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuSbS2\\n\",\n        \"output\": \" No, CuSbS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Re3As7\\n\",\n        \"output\": \" Yes, Re3As7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrAg\\n\",\n        \"output\": \" Yes, SrAg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BSe2Cl\\n\",\n        \"output\": \" Yes, BSe2Cl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbLiCO3\\n\",\n        \"output\": \" No, RbLiCO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiO2\\n\",\n        \"output\": \" No, TiO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ho3GaC\\n\",\n        \"output\": \" Yes, Ho3GaC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrInRh2\\n\",\n        \"output\": \" Yes, ZrInRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3Cd(SnS4)2\\n\",\n        \"output\": \" No, Ba3Cd(SnS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiO\\n\",\n        \"output\": \" Yes, BiO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al0.1In0.9P1\\n\",\n        \"output\": \" No, Al0.1In0.9P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaSn2S5\\n\",\n        \"output\": \" No, BaSn2S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd1Se0.99S0.01\\n\",\n        \"output\": \" No, Cd1Se0.99S0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K10Co4Sn4S17\\n\",\n        \"output\": \" No, K10Co4Sn4S17 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbPmPt2\\n\",\n        \"output\": \" Yes, YbPmPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2Cu(PO4)3\\n\",\n        \"output\": \" Yes, Mn2Cu(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.1Ga0.9As0.9P0.1\\n\",\n        \"output\": \" No, In0.1Ga0.9As0.9P0.1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Re3P4\\n\",\n        \"output\": \" Yes, Re3P4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.5Ga0.5P1\\n\",\n        \"output\": \" No, In0.5Ga0.5P1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeAl2Pd5\\n\",\n        \"output\": \" Yes, CeAl2Pd5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbPPbO4\\n\",\n        \"output\": \" No, RbPPbO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrAl\\n\",\n        \"output\": \" Yes, SrAl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaSe\\n\",\n        \"output\": \" No, BaSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Dy2CuOs\\n\",\n        \"output\": \" Yes, Dy2CuOs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ni(CN)2\\n\",\n        \"output\": \" No, Ni(CN)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1.65Cu0.35Se2.65\\n\",\n        \"output\": \" No, In1.65Cu0.35Se2.65 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiIO\\n\",\n        \"output\": \" No, BiIO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VAg(IO4)2\\n\",\n        \"output\": \" No, VAg(IO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ta4N5\\n\",\n        \"output\": \" Yes, Ta4N5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2ErInSe5\\n\",\n        \"output\": \" No, Ba2ErInSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb4Co2PdSe12\\n\",\n        \"output\": \" Yes, Nb4Co2PdSe12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na2Pt(IO3)6\\n\",\n        \"output\": \" No, Na2Pt(IO3)6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1.01Cu0.99Se2.01\\n\",\n        \"output\": \" No, Ga1.01Cu0.99Se2.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ErNi4B\\n\",\n        \"output\": \" Yes, ErNi4B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdTiGe\\n\",\n        \"output\": \" Yes, NdTiGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3GeS5\\n\",\n        \"output\": \" No, Ba3GeS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbRh2\\n\",\n        \"output\": \" Yes, YbRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KFeCuTe2\\n\",\n        \"output\": \" No, KFeCuTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" denim\\n\",\n        \"output\": \" denim is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2AgPS4\\n\",\n        \"output\": \" No, Rb2AgPS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AlBi\\n\",\n        \"output\": \" No, AlBi is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba8Hg4Se7S5\\n\",\n        \"output\": \" No, Ba8Hg4Se7S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" GdZnIn\\n\",\n        \"output\": \" Yes, GdZnIn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3B1.5Sb0.5S6\\n\",\n        \"output\": \" No, Ba3B1.5Sb0.5S6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr2Te4O11\\n\",\n        \"output\": \" No, Pr2Te4O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YbZnPt\\n\",\n        \"output\": \" Yes, YbZnPt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce(AlZn)2\\n\",\n        \"output\": \" Yes, Ce(AlZn)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr2Se\\n\",\n        \"output\": \" Yes, Zr2Se is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sr2La2.58Bi5.42S14\\n\",\n        \"output\": \" No, Sr2La2.58Bi5.42S14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cd1Se0.65S0.35\\n\",\n        \"output\": \" No, Cd1Se0.65S0.35 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba5Ga6SnP12\\n\",\n        \"output\": \" No, Ba5Ga6SnP12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sb8I2O11\\n\",\n        \"output\": \" No, Sb8I2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs3Bi2Br9\\n\",\n        \"output\": \" No, Cs3Bi2Br9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrBiClO2\\n\",\n        \"output\": \" No, SrBiClO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ho(BiO3)2\\n\",\n        \"output\": \" Yes, Ho(BiO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" FeAgSe2\\n\",\n        \"output\": \" No, FeAgSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnSi(AgS2)2\\n\",\n        \"output\": \" No, ZnSi(AgS2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Lu5Si3B\\n\",\n        \"output\": \" Yes, Lu5Si3B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrHg4(AsCl3)2\\n\",\n        \"output\": \" No, ZrHg4(AsCl3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" mint\\n\",\n        \"output\": \" mint is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiGd5P2O13\\n\",\n        \"output\": \" No, LiGd5P2O13 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs4In8GeSe16\\n\",\n        \"output\": \" No, Cs4In8GeSe16 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ni2PO5\\n\",\n        \"output\": \" Yes, Ni2PO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErAlGe\\n\",\n        \"output\": \" Yes, ErAlGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg3(Ni10P3)2\\n\",\n        \"output\": \" Yes, Mg3(Ni10P3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CuBi(PSe3)2\\n\",\n        \"output\": \" No, CuBi(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2GdGaSe5\\n\",\n        \"output\": \" No, Ba2GdGaSe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VNi5(PO4)6\\n\",\n        \"output\": \" Yes, VNi5(PO4)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl0.04Te1Pb0.96\\n\",\n        \"output\": \" No, Tl0.04Te1Pb0.96 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" P2Pd3S8\\n\",\n        \"output\": \" No, P2Pd3S8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiIn(IO3)4\\n\",\n        \"output\": \" No, LiIn(IO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeMoO4F\\n\",\n        \"output\": \" No, CeMoO4F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd(PRu)2\\n\",\n        \"output\": \" Yes, Nd(PRu)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" PdSe\\n\",\n        \"output\": \" No, PdSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li14Ti21O48\\n\",\n        \"output\": \" Yes, Li14Ti21O48 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YVSeO10\\n\",\n        \"output\": \" No, YVSeO10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K8Ce2I18O53\\n\",\n        \"output\": \" No, K8Ce2I18O53 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SrZr2Nb\\n\",\n        \"output\": \" Yes, SrZr2Nb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.15Te0.15Pb0.85Se0.85\\n\",\n        \"output\": \" No, Sn0.15Te0.15Pb0.85Se0.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4Si3Se9Cl2\\n\",\n        \"output\": \" No, Ba4Si3Se9Cl2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" NdIn5Rh\\n\",\n        \"output\": \" Yes, NdIn5Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsSn3\\n\",\n        \"output\": \" Yes, CsSn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" DyInPt2\\n\",\n        \"output\": \" Yes, DyInPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" U5Ge3\\n\",\n        \"output\": \" Yes, U5Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" criminal\\n\",\n        \"output\": \" criminal is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaSnO3\\n\",\n        \"output\": \" No, BaSnO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf6PbO18\\n\",\n        \"output\": \" Yes, Hf6PbO18 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr6Al2Ni\\n\",\n        \"output\": \" Yes, Zr6Al2Ni is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu2OF2\\n\",\n        \"output\": \" Yes, Cu2OF2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V3Pb2Se5O18\\n\",\n        \"output\": \" No, V3Pb2Se5O18 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Dy2CdPd2\\n\",\n        \"output\": \" Yes, Dy2CdPd2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HoGe\\n\",\n        \"output\": \" Yes, HoGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr2Te\\n\",\n        \"output\": \" Yes, Zr2Te is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca5Sb3\\n\",\n        \"output\": \" Yes, Ca5Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ukraine\\n\",\n        \"output\": \" ukraine is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Hg3Bi2(SCl4)2\\n\",\n        \"output\": \" No, Hg3Bi2(SCl4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs3Sb\\n\",\n        \"output\": \" No, Cs3Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Fe2Cu(PO4)3\\n\",\n        \"output\": \" Yes, Fe2Cu(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In2GeTe3\\n\",\n        \"output\": \" No, In2GeTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PmDy3\\n\",\n        \"output\": \" Yes, PmDy3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd0.1In0.9Te0.1As0.9\\n\",\n        \"output\": \" No, Cd0.1In0.9Te0.1As0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BiSbTe3\\n\",\n        \"output\": \" No, BiSbTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pt3PbC\\n\",\n        \"output\": \" Yes, Pt3PbC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hf3P\\n\",\n        \"output\": \" Yes, Hf3P is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb1.45Sb7.45Pb3.1Se15\\n\",\n        \"output\": \" No, Rb1.45Sb7.45Pb3.1Se15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" UCuP2\\n\",\n        \"output\": \" Yes, UCuP2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScCoO3\\n\",\n        \"output\": \" Yes, ScCoO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ThRu3C\\n\",\n        \"output\": \" Yes, ThRu3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb2O3\\n\",\n        \"output\": \" No, Yb2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs3V2Cl9\\n\",\n        \"output\": \" Yes, Cs3V2Cl9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KB5PbO9\\n\",\n        \"output\": \" No, KB5PbO9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1.85Cu0.15Se2.85\\n\",\n        \"output\": \" No, In1.85Cu0.15Se2.85 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ti2B\\n\",\n        \"output\": \" Yes, Ti2B is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2SnS4\\n\",\n        \"output\": \" No, Ca2SnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3BSbSe6\\n\",\n        \"output\": \" No, Ba3BSbSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca5B3O9F\\n\",\n        \"output\": \" No, Ca5B3O9F is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuVO4\\n\",\n        \"output\": \" No, EuVO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiCuPO4\\n\",\n        \"output\": \" Yes, LiCuPO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SmB(SbO4)2\\n\",\n        \"output\": \" No, SmB(SbO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg2Zr14O5\\n\",\n        \"output\": \" Yes, Mg2Zr14O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Nd2Ru2O7\\n\",\n        \"output\": \" Yes, Nd2Ru2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na5Gd(MoO4)4\\n\",\n        \"output\": \" No, Na5Gd(MoO4)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1Sb0.2As0.8\\n\",\n        \"output\": \" No, In1Sb0.2As0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErSe2\\n\",\n        \"output\": \" No, ErSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2GaBiTe5\\n\",\n        \"output\": \" No, Ba2GaBiTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Fe3N\\n\",\n        \"output\": \" Yes, Fe3N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TeAs\\n\",\n        \"output\": \" No, TeAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CeSiIr\\n\",\n        \"output\": \" Yes, CeSiIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In1Ag1.75Sb5.75Se11\\n\",\n        \"output\": \" No, In1Ag1.75Sb5.75Se11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In0.72Ga0.28As1\\n\",\n        \"output\": \" No, In0.72Ga0.28As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbCuPdF5\\n\",\n        \"output\": \" Yes, RbCuPdF5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TbCo2\\n\",\n        \"output\": \" Yes, TbCo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na0.8Li0.2As1Se2\\n\",\n        \"output\": \" No, Na0.8Li0.2As1Se2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Na2Ge2Se5\\n\",\n        \"output\": \" No, Na2Ge2Se5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga0.01Te1Pb0.99\\n\",\n        \"output\": \" No, Ga0.01Te1Pb0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Eu(DySe2)2\\n\",\n        \"output\": \" No, Eu(DySe2)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NaInS2\\n\",\n        \"output\": \" No, NaInS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2SmTaO6\\n\",\n        \"output\": \" No, Ca2SmTaO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi24BO39\\n\",\n        \"output\": \" No, Bi24BO39 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sn0.1Te1Pb0.9\\n\",\n        \"output\": \" No, Sn0.1Te1Pb0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd6Ta4Al43\\n\",\n        \"output\": \" Yes, Gd6Ta4Al43 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MgTi4O6\\n\",\n        \"output\": \" Yes, MgTi4O6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe2B(PO4)3\\n\",\n        \"output\": \" No, Fe2B(PO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu2WSe4\\n\",\n        \"output\": \" No, Cu2WSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BiSI\\n\",\n        \"output\": \" No, BiSI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mn3Al10\\n\",\n        \"output\": \" Yes, Mn3Al10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KLu\\n\",\n        \"output\": \" Yes, KLu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb2SmS4\\n\",\n        \"output\": \" Yes, Yb2SmS4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbGaSnSe4\\n\",\n        \"output\": \" No, RbGaSnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SbPb2S2I3\\n\",\n        \"output\": \" No, SbPb2S2I3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu2Mo2C3\\n\",\n        \"output\": \" Yes, Lu2Mo2C3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaF2\\n\",\n        \"output\": \" No, CaF2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In1.7Cu0.3Se2.7\\n\",\n        \"output\": \" No, In1.7Cu0.3Se2.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sr2V3Se5O18\\n\",\n        \"output\": \" No, Sr2V3Se5O18 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RhSeS\\n\",\n        \"output\": \" No, RhSeS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Rb2FeI4\\n\",\n        \"output\": \" Yes, Rb2FeI4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2CoAs\\n\",\n        \"output\": \" Yes, Mn2CoAs is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd3Sb2\\n\",\n        \"output\": \" No, Cd3Sb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CeN\\n\",\n        \"output\": \" No, CeN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbPdF3\\n\",\n        \"output\": \" Yes, RbPdF3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2FeReO6\\n\",\n        \"output\": \" Yes, Ba2FeReO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La2YbCuS5\\n\",\n        \"output\": \" No, La2YbCuS5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiMn(PO4)2\\n\",\n        \"output\": \" Yes, LiMn(PO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al2S3\\n\",\n        \"output\": \" No, Al2S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge2Os\\n\",\n        \"output\": \" Yes, Ge2Os is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuAlAg2\\n\",\n        \"output\": \" Yes, LuAlAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" B2Se2O7\\n\",\n        \"output\": \" No, B2Se2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdErTl2\\n\",\n        \"output\": \" Yes, NdErTl2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn15Si26\\n\",\n        \"output\": \" No, Mn15Si26 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrIrO6\\n\",\n        \"output\": \" Yes, CrIrO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrF3\\n\",\n        \"output\": \" No, PrF3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2Cu4Sn5\\n\",\n        \"output\": \" Yes, Sm2Cu4Sn5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2Te0.4Se2.6\\n\",\n        \"output\": \" No, Bi2Te0.4Se2.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zr5Sn4\\n\",\n        \"output\": \" Yes, Zr5Sn4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiCa2Ge3\\n\",\n        \"output\": \" Yes, LiCa2Ge3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" GeRh\\n\",\n        \"output\": \" Yes, GeRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba5Cd(Ga2Se5)3\\n\",\n        \"output\": \" No, Ba5Cd(Ga2Se5)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sn0.28Te0.28Pb0.72Se0.72\\n\",\n        \"output\": \" No, Sn0.28Te0.28Pb0.72Se0.72 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In0.7Ga0.3As0.3P0.7\\n\",\n        \"output\": \" No, In0.7Ga0.3As0.3P0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg2GeSe4\\n\",\n        \"output\": \" No, Mg2GeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In2Cu1S3.5\\n\",\n        \"output\": \" No, In2Cu1S3.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" W2N\\n\",\n        \"output\": \" Yes, W2N is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" refrigerator\\n\",\n        \"output\": \" refrigerator is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiMnCoO4\\n\",\n        \"output\": \" Yes, LiMnCoO4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K3LiNb6O15\\n\",\n        \"output\": \" Yes, K3LiNb6O15 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GeAs2\\n\",\n        \"output\": \" No, GeAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KAgO\\n\",\n        \"output\": \" Yes, KAgO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlInTe2\\n\",\n        \"output\": \" No, TlInTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" rainbow\\n\",\n        \"output\": \" rainbow is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Fe(PdSe)2\\n\",\n        \"output\": \" Yes, Fe(PdSe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YAlPd\\n\",\n        \"output\": \" Yes, YAlPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CaPd3C\\n\",\n        \"output\": \" Yes, CaPd3C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiTa3(BiO3)4\\n\",\n        \"output\": \" No, LiTa3(BiO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" spoon\\n\",\n        \"output\": \" spoon is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2V2F7\\n\",\n        \"output\": \" Yes, Li2V2F7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" DySnRu2\\n\",\n        \"output\": \" Yes, DySnRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ErHg2\\n\",\n        \"output\": \" Yes, ErHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KBaSbSe3\\n\",\n        \"output\": \" No, KBaSbSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YH2\\n\",\n        \"output\": \" Yes, YH2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LuHfRu2\\n\",\n        \"output\": \" Yes, LuHfRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pb3Se2(BrO3)2\\n\",\n        \"output\": \" No, Pb3Se2(BrO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tb10B7C10\\n\",\n        \"output\": \" Yes, Tb10B7C10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbYbHg2\\n\",\n        \"output\": \" Yes, TbYbHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuPd\\n\",\n        \"output\": \" Yes, EuPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cu6PbO8\\n\",\n        \"output\": \" Yes, Cu6PbO8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BeGaRh2\\n\",\n        \"output\": \" Yes, BeGaRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbU2SbS8\\n\",\n        \"output\": \" Yes, RbU2SbS8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho4C7\\n\",\n        \"output\": \" Yes, Ho4C7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y(CuTe)3\\n\",\n        \"output\": \" No, Y(CuTe)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbPbBrO2\\n\",\n        \"output\": \" No, SbPbBrO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La6Sb4(SO4)3\\n\",\n        \"output\": \" No, La6Sb4(SO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sc3BPb\\n\",\n        \"output\": \" Yes, Sc3BPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YMg4Cu\\n\",\n        \"output\": \" Yes, YMg4Cu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cu1.8S1\\n\",\n        \"output\": \" No, Cu1.8S1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al13Ru4\\n\",\n        \"output\": \" Yes, Al13Ru4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HgBr\\n\",\n        \"output\": \" No, HgBr is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm2O3\\n\",\n        \"output\": \" No, Tm2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbMgPd\\n\",\n        \"output\": \" Yes, YbMgPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" V3(HO2)4\\n\",\n        \"output\": \" Yes, V3(HO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al2Cr2O7\\n\",\n        \"output\": \" Yes, Al2Cr2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RbAg5(PS4)2\\n\",\n        \"output\": \" No, RbAg5(PS4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ce1Mn0.5Se1O1\\n\",\n        \"output\": \" No, Ce1Mn0.5Se1O1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.5Ga0.5As0.5P0.5\\n\",\n        \"output\": \" No, In0.5Ga0.5As0.5P0.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiMgAs\\n\",\n        \"output\": \" No, LiMgAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb(CuS)3\\n\",\n        \"output\": \" No, Yb(CuS)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In0.01Ga0.99As0.99P0.01\\n\",\n        \"output\": \" No, In0.01Ga0.99As0.99P0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1Sb0.25As0.75\\n\",\n        \"output\": \" No, Ga1Sb0.25As0.75 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiH3(SeO3)2\\n\",\n        \"output\": \" No, LiH3(SeO3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" EuCd11\\n\",\n        \"output\": \" Yes, EuCd11 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SmSi3Pt5\\n\",\n        \"output\": \" Yes, SmSi3Pt5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pb2O3\\n\",\n        \"output\": \" No, Pb2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsTaPSe6\\n\",\n        \"output\": \" No, CsTaPSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TmScHg2\\n\",\n        \"output\": \" Yes, TmScHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc2Al3Ru\\n\",\n        \"output\": \" Yes, Sc2Al3Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TiSe2\\n\",\n        \"output\": \" No, TiSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaLa2Te5O14\\n\",\n        \"output\": \" No, BaLa2Te5O14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbSI\\n\",\n        \"output\": \" No, SbSI is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Co(PO3)4\\n\",\n        \"output\": \" Yes, Co(PO3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ce3AlC\\n\",\n        \"output\": \" Yes, Ce3AlC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErB2Ru3\\n\",\n        \"output\": \" Yes, ErB2Ru3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbSnAu\\n\",\n        \"output\": \" Yes, TbSnAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdInAu\\n\",\n        \"output\": \" Yes, NdInAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaTi14O28\\n\",\n        \"output\": \" Yes, BaTi14O28 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ga1Sb0.8As0.2\\n\",\n        \"output\": \" No, Ga1Sb0.8As0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ce1.3Lu0.7S3\\n\",\n        \"output\": \" No, Ce1.3Lu0.7S3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cs2Sn(PSe3)2\\n\",\n        \"output\": \" No, Cs2Sn(PSe3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" kimberly\\n\",\n        \"output\": \" kimberly is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbInTe3O8\\n\",\n        \"output\": \" No, RbInTe3O8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tm2IrPd\\n\",\n        \"output\": \" Yes, Tm2IrPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" approval\\n\",\n        \"output\": \" approval is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tl0.01Te1Pb0.99\\n\",\n        \"output\": \" No, Tl0.01Te1Pb0.99 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaMn4O7\\n\",\n        \"output\": \" Yes, BaMn4O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nd3AlC\\n\",\n        \"output\": \" Yes, Nd3AlC is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hg2Rh\\n\",\n        \"output\": \" Yes, Hg2Rh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoSb2\\n\",\n        \"output\": \" Yes, HoSb2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BAs\\n\",\n        \"output\": \" No, BAs is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TmB2C\\n\",\n        \"output\": \" Yes, TmB2C is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" UGa2\\n\",\n        \"output\": \" Yes, UGa2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg2Cu\\n\",\n        \"output\": \" Yes, Mg2Cu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy2Sn5\\n\",\n        \"output\": \" Yes, Dy2Sn5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TbNi5\\n\",\n        \"output\": \" Yes, TbNi5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TaTl3S4\\n\",\n        \"output\": \" No, TaTl3S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba2SmGaTe5\\n\",\n        \"output\": \" No, Ba2SmGaTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mg23Al30\\n\",\n        \"output\": \" Yes, Mg23Al30 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CaZn3\\n\",\n        \"output\": \" Yes, CaZn3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrSeO4\\n\",\n        \"output\": \" No, SrSeO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U2AlCo3\\n\",\n        \"output\": \" Yes, U2AlCo3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" VCu3(PO4)4\\n\",\n        \"output\": \" Yes, VCu3(PO4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Gd2Mn4S7\\n\",\n        \"output\": \" No, Gd2Mn4S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" YAlGe\\n\",\n        \"output\": \" Yes, YAlGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsInSnS4\\n\",\n        \"output\": \" No, CsInSnS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2Nb2N2O5\\n\",\n        \"output\": \" Yes, La2Nb2N2O5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KC60\\n\",\n        \"output\": \" Yes, KC60 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li4Mn5Ni3O16\\n\",\n        \"output\": \" Yes, Li4Mn5Ni3O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiGaSe2\\n\",\n        \"output\": \" No, LiGaSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" BMo\\n\",\n        \"output\": \" Yes, BMo is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K2VAgS4\\n\",\n        \"output\": \" No, K2VAgS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TlSbTe3\\n\",\n        \"output\": \" No, TlSbTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeSi2Pt\\n\",\n        \"output\": \" Yes, CeSi2Pt is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YSiNi\\n\",\n        \"output\": \" Yes, YSiNi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" As2Se3\\n\",\n        \"output\": \" No, As2Se3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" EuRhO3\\n\",\n        \"output\": \" Yes, EuRhO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdB(SbO4)2\\n\",\n        \"output\": \" No, GdB(SbO4)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Y2AlZn\\n\",\n        \"output\": \" Yes, Y2AlZn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li3Ti3(PO4)4\\n\",\n        \"output\": \" Yes, Li3Ti3(PO4)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1As0.2P0.8\\n\",\n        \"output\": \" No, Ga1As0.2P0.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" KGaSnSe4\\n\",\n        \"output\": \" No, KGaSnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Co(WO4)2\\n\",\n        \"output\": \" Yes, Co(WO4)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cd4P2Cl3\\n\",\n        \"output\": \" No, Cd4P2Cl3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga8Cu3Mo2\\n\",\n        \"output\": \" Yes, Ga8Cu3Mo2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd4P2Br3\\n\",\n        \"output\": \" No, Cd4P2Br3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsSmCdSe3\\n\",\n        \"output\": \" No, CsSmCdSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaGe2\\n\",\n        \"output\": \" No, BaGe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er(InS2)3\\n\",\n        \"output\": \" No, Er(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K6CdTe4\\n\",\n        \"output\": \" No, K6CdTe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiSbTe2\\n\",\n        \"output\": \" No, LiSbTe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" In(MoSe)3\\n\",\n        \"output\": \" Yes, In(MoSe)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdInIr\\n\",\n        \"output\": \" Yes, GdInIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" KBiS2\\n\",\n        \"output\": \" No, KBiS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Er2SnAu2\\n\",\n        \"output\": \" Yes, Er2SnAu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KIO3\\n\",\n        \"output\": \" No, KIO3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1Sb0.8As0.2\\n\",\n        \"output\": \" No, In1Sb0.8As0.2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sm2RuAu\\n\",\n        \"output\": \" Yes, Sm2RuAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li0.5Ge1Pb1.75S4\\n\",\n        \"output\": \" No, Li0.5Ge1Pb1.75S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfCo3B2\\n\",\n        \"output\": \" Yes, HfCo3B2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu3AsS4\\n\",\n        \"output\": \" No, Cu3AsS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiBi2(PO4)3\\n\",\n        \"output\": \" Yes, LiBi2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In4As5(BrO4)3\\n\",\n        \"output\": \" No, In4As5(BrO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li6Fe9CoO20\\n\",\n        \"output\": \" Yes, Li6Fe9CoO20 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ge0.06Te0.06Pb0.94Se0.94\\n\",\n        \"output\": \" No, Ge0.06Te0.06Pb0.94Se0.94 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" UO\\n\",\n        \"output\": \" No, UO is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" TaInNi\\n\",\n        \"output\": \" Yes, TaInNi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" dorothy\\n\",\n        \"output\": \" dorothy is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CrCoPt2\\n\",\n        \"output\": \" Yes, CrCoPt2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2In\\n\",\n        \"output\": \" Yes, Sm2In is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoTiGe\\n\",\n        \"output\": \" Yes, HoTiGe is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiY2Ru\\n\",\n        \"output\": \" Yes, LiY2Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" MnP4\\n\",\n        \"output\": \" No, MnP4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Si0.3Ge0.7\\n\",\n        \"output\": \" No, Si0.3Ge0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbH2\\n\",\n        \"output\": \" Yes, TbH2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Mn5Ge2\\n\",\n        \"output\": \" Yes, Mn5Ge2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba2FeMoO6\\n\",\n        \"output\": \" Yes, Ba2FeMoO6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Hg2Sb2O7\\n\",\n        \"output\": \" Yes, Hg2Sb2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SrTlHg2\\n\",\n        \"output\": \" Yes, SrTlHg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K4GeSe4\\n\",\n        \"output\": \" No, K4GeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NaZrCuTe3\\n\",\n        \"output\": \" Yes, NaZrCuTe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg32Al36Ag13\\n\",\n        \"output\": \" Yes, Mg32Al36Ag13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Mg3Ru2\\n\",\n        \"output\": \" Yes, Mg3Ru2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ta6Be15Cu8\\n\",\n        \"output\": \" Yes, Ta6Be15Cu8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cr2O3\\n\",\n        \"output\": \" No, Cr2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnSi\\n\",\n        \"output\": \" No, MnSi is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba3Ta5NO14\\n\",\n        \"output\": \" No, Ba3Ta5NO14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ge0.01Te0.99Pb0.99S0.01\\n\",\n        \"output\": \" No, Ge0.01Te0.99Pb0.99S0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2In3CuSe6\\n\",\n        \"output\": \" No, K2In3CuSe6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nd2IrPd\\n\",\n        \"output\": \" Yes, Nd2IrPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ta22(CuS12)3\\n\",\n        \"output\": \" Yes, Ta22(CuS12)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sm2TlHg\\n\",\n        \"output\": \" Yes, Sm2TlHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li4V5Cu3O16\\n\",\n        \"output\": \" Yes, Li4V5Cu3O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" authorisation\\n\",\n        \"output\": \" authorisation is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Bi4Pd(SeO3)4\\n\",\n        \"output\": \" No, Bi4Pd(SeO3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" MnSbRh2\\n\",\n        \"output\": \" Yes, MnSbRh2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn0.9Ga0.1P0.1Se0.9\\n\",\n        \"output\": \" No, Zn0.9Ga0.1P0.1Se0.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr2HgPb\\n\",\n        \"output\": \" Yes, Pr2HgPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SbTeRu\\n\",\n        \"output\": \" No, SbTeRu is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In1.05Cu0.95Se2.05\\n\",\n        \"output\": \" No, In1.05Cu0.95Se2.05 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2Sn3(SbS5)2\\n\",\n        \"output\": \" No, Cs2Sn3(SbS5)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfHg4(PCl3)2\\n\",\n        \"output\": \" No, HfHg4(PCl3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsK2Sb\\n\",\n        \"output\": \" No, CsK2Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga1.9Cu0.1S2.9\\n\",\n        \"output\": \" No, Ga1.9Cu0.1S2.9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2GdGaTe5\\n\",\n        \"output\": \" No, Ba2GdGaTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb2O5\\n\",\n        \"output\": \" No, Nb2O5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TcS2\\n\",\n        \"output\": \" No, TcS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" VIr\\n\",\n        \"output\": \" Yes, VIr is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La3GaCuSe7\\n\",\n        \"output\": \" No, La3GaCuSe7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2Ge2Se7\\n\",\n        \"output\": \" No, La2Ge2Se7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Pr(FeSi)2\\n\",\n        \"output\": \" Yes, Pr(FeSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Mn(NiO3)2\\n\",\n        \"output\": \" Yes, Li3Mn(NiO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ni3S4\\n\",\n        \"output\": \" Yes, Ni3S4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ga2Cu1S3.5\\n\",\n        \"output\": \" No, Ga2Cu1S3.5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" VZn2BiO6\\n\",\n        \"output\": \" No, VZn2BiO6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" YbH2ClO2\\n\",\n        \"output\": \" Yes, YbH2ClO2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tl3Ir\\n\",\n        \"output\": \" Yes, Tl3Ir is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbTmO3\\n\",\n        \"output\": \" Yes, RbTmO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" LiY(CuP)2\\n\",\n        \"output\": \" Yes, LiY(CuP)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Te0.99Pb1Se0.01\\n\",\n        \"output\": \" No, Te0.99Pb1Se0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Na2EuGeSe4\\n\",\n        \"output\": \" No, Na2EuGeSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Hf5Sb9\\n\",\n        \"output\": \" Yes, Hf5Sb9 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Tm4In(NiGe2)2\\n\",\n        \"output\": \" Yes, Tm4In(NiGe2)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HfAsRh\\n\",\n        \"output\": \" Yes, HfAsRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb2HgPb\\n\",\n        \"output\": \" Yes, Yb2HgPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ho2(MoO4)3\\n\",\n        \"output\": \" No, Ho2(MoO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr7Sb4\\n\",\n        \"output\": \" Yes, Zr7Sb4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Cu23(Sb4S13)2\\n\",\n        \"output\": \" Yes, Cu23(Sb4S13)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" SiTe2Os\\n\",\n        \"output\": \" Yes, SiTe2Os is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" InP\\n\",\n        \"output\": \" No, InP is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CsGeB3O7\\n\",\n        \"output\": \" No, CsGeB3O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Y4C7\\n\",\n        \"output\": \" Yes, Y4C7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca2CdAs2\\n\",\n        \"output\": \" No, Ca2CdAs2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Bi2O3\\n\",\n        \"output\": \" No, Bi2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Al0.99Cd0.01Sb0.99Te0.01\\n\",\n        \"output\": \" No, Al0.99Cd0.01Sb0.99Te0.01 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Gd6Ge2.5S14\\n\",\n        \"output\": \" No, Gd6Ge2.5S14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" plot\\n\",\n        \"output\": \" plot is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Zn3N2\\n\",\n        \"output\": \" Yes, Zn3N2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NbOsPb\\n\",\n        \"output\": \" Yes, NbOsPb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" PrAu\\n\",\n        \"output\": \" Yes, PrAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" P2H12N7Cl\\n\",\n        \"output\": \" Yes, P2H12N7Cl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs4Zr3S14\\n\",\n        \"output\": \" No, Cs4Zr3S14 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs3Nb9(TeO8)4\\n\",\n        \"output\": \" No, Cs3Nb9(TeO8)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.12Ge0.88\\n\",\n        \"output\": \" No, Si0.12Ge0.88 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ScGe2\\n\",\n        \"output\": \" Yes, ScGe2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" V5SiB2\\n\",\n        \"output\": \" Yes, V5SiB2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BiP3(PbO4)3\\n\",\n        \"output\": \" No, BiP3(PbO4)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Rb2Tb3AlF16\\n\",\n        \"output\": \" Yes, Rb2Tb3AlF16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmAlCu\\n\",\n        \"output\": \" Yes, SmAlCu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Nd2Ti3O10\\n\",\n        \"output\": \" No, K2Nd2Ti3O10 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" HfVSi\\n\",\n        \"output\": \" Yes, HfVSi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Zr1.33Ta0.67N1.63O1.89\\n\",\n        \"output\": \" No, Zr1.33Ta0.67N1.63O1.89 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsYHgSe3\\n\",\n        \"output\": \" No, CsYHgSe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RuS2\\n\",\n        \"output\": \" No, RuS2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CoOF\\n\",\n        \"output\": \" Yes, CoOF is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cd4Sb3\\n\",\n        \"output\": \" No, Cd4Sb3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ca(TiS2)4\\n\",\n        \"output\": \" Yes, Ca(TiS2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Fe12As5\\n\",\n        \"output\": \" Yes, Fe12As5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" RePO5\\n\",\n        \"output\": \" Yes, RePO5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" U(MnSi)2\\n\",\n        \"output\": \" Yes, U(MnSi)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" KSi2P3\\n\",\n        \"output\": \" No, KSi2P3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbNa2Sb\\n\",\n        \"output\": \" No, RbNa2Sb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" As2Rh\\n\",\n        \"output\": \" No, As2Rh is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" K6Yb3(PS4)5\\n\",\n        \"output\": \" No, K6Yb3(PS4)5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Sn0.08Te1Pb0.92\\n\",\n        \"output\": \" No, Sn0.08Te1Pb0.92 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mn2Nb\\n\",\n        \"output\": \" Yes, Mn2Nb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg5As\\n\",\n        \"output\": \" Yes, Mg5As is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" AlCuSe2\\n\",\n        \"output\": \" No, AlCuSe2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" bait\\n\",\n        \"output\": \" bait is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Mo2Se2O11\\n\",\n        \"output\": \" No, Li2Mo2Se2O11 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" border\\n\",\n        \"output\": \" border is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba(ZnAs)2\\n\",\n        \"output\": \" No, Ba(ZnAs)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" RbGe3\\n\",\n        \"output\": \" Yes, RbGe3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZnCu2SiS4\\n\",\n        \"output\": \" No, ZnCu2SiS4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2MgSn3Se8\\n\",\n        \"output\": \" No, Cs2MgSn3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuP2(HO3)2\\n\",\n        \"output\": \" Yes, CuP2(HO3)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdMnSbO\\n\",\n        \"output\": \" Yes, NdMnSbO is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" GdN\\n\",\n        \"output\": \" No, GdN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CsGaSnSe4\\n\",\n        \"output\": \" No, CsGaSnSe4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Si0.08Ge0.92\\n\",\n        \"output\": \" No, Si0.08Ge0.92 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" TiTc2Sb\\n\",\n        \"output\": \" Yes, TiTc2Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La5YbS8\\n\",\n        \"output\": \" Yes, La5YbS8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" La3Ga1Ge0.5S7\\n\",\n        \"output\": \" No, La3Ga1Ge0.5S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Dy(InS2)3\\n\",\n        \"output\": \" No, Dy(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zr1.86Cu1S4\\n\",\n        \"output\": \" No, Zr1.86Cu1S4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" NdMgNi4\\n\",\n        \"output\": \" Yes, NdMgNi4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba4Si20Au3\\n\",\n        \"output\": \" Yes, Ba4Si20Au3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ZrAlRu2\\n\",\n        \"output\": \" Yes, ZrAlRu2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sr2GeN2\\n\",\n        \"output\": \" Yes, Sr2GeN2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrO2\\n\",\n        \"output\": \" No, ZrO2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Nb2Sb\\n\",\n        \"output\": \" Yes, Nb2Sb is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiZn2GaO4\\n\",\n        \"output\": \" No, LiZn2GaO4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga2GeTe3\\n\",\n        \"output\": \" No, Ga2GeTe3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CrSi2\\n\",\n        \"output\": \" No, CrSi2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" YbSb\\n\",\n        \"output\": \" No, YbSb is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" K1.46Sn3.09Bi7.45Se15\\n\",\n        \"output\": \" No, K1.46Sn3.09Bi7.45Se15 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" author\\n\",\n        \"output\": \" author is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Gd(InS2)3\\n\",\n        \"output\": \" No, Gd(InS2)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Na4Eu(GeS3)2\\n\",\n        \"output\": \" No, Na4Eu(GeS3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" SmTe\\n\",\n        \"output\": \" No, SmTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li2Si4Ni5O14\\n\",\n        \"output\": \" Yes, Li2Si4Ni5O14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1.8Cu0.2S2.8\\n\",\n        \"output\": \" No, Ga1.8Cu0.2S2.8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" cod\\n\",\n        \"output\": \" cod is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K3Th2Cu3S7\\n\",\n        \"output\": \" No, K3Th2Cu3S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" In2Te\\n\",\n        \"output\": \" No, In2Te is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" K2Al2B2O7\\n\",\n        \"output\": \" No, K2Al2B2O7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Al6Ru\\n\",\n        \"output\": \" Yes, Al6Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2LaTl\\n\",\n        \"output\": \" Yes, Li2LaTl is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" La(Ni2B)6\\n\",\n        \"output\": \" Yes, La(Ni2B)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" NdInCu\\n\",\n        \"output\": \" Yes, NdInCu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CoSb2\\n\",\n        \"output\": \" No, CoSb2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Sb2O3\\n\",\n        \"output\": \" No, Sb2O3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" BaTe\\n\",\n        \"output\": \" No, BaTe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Eu(MnGe)2\\n\",\n        \"output\": \" Yes, Eu(MnGe)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HgSe\\n\",\n        \"output\": \" No, HgSe is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Pm2IrRh\\n\",\n        \"output\": \" Yes, Pm2IrRh is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Li2Nb2(PO4)3\\n\",\n        \"output\": \" Yes, Li2Nb2(PO4)3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" UGaNi\\n\",\n        \"output\": \" Yes, UGaNi is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" orchestra\\n\",\n        \"output\": \" orchestra is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ZrTaN3\\n\",\n        \"output\": \" No, ZrTaN3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Li4Mn5Nb3O16\\n\",\n        \"output\": \" Yes, Li4Mn5Nb3O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbCd4In5Se12\\n\",\n        \"output\": \" No, RbCd4In5Se12 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tl2BiP2S7\\n\",\n        \"output\": \" No, Tl2BiP2S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScN\\n\",\n        \"output\": \" No, ScN is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Zn0.75Hg0.25Se1\\n\",\n        \"output\": \" No, Zn0.75Hg0.25Se1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CdPd\\n\",\n        \"output\": \" Yes, CdPd is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" CsAgSb4S7\\n\",\n        \"output\": \" No, CsAgSb4S7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TbBe13\\n\",\n        \"output\": \" Yes, TbBe13 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ba3Sn0.87Bi2.13Se8\\n\",\n        \"output\": \" No, Ba3Sn0.87Bi2.13Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" MgScAg2\\n\",\n        \"output\": \" Yes, MgScAg2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Pr9(SbO)5\\n\",\n        \"output\": \" Yes, Pr9(SbO)5 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" LiCaO3\\n\",\n        \"output\": \" Yes, LiCaO3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb3Ti3O14\\n\",\n        \"output\": \" Yes, Yb3Ti3O14 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Sc(GaFe)6\\n\",\n        \"output\": \" Yes, Sc(GaFe)6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Rb2Cd3(B4O7)4\\n\",\n        \"output\": \" No, Rb2Cd3(B4O7)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" BaTeMo2O9\\n\",\n        \"output\": \" No, BaTeMo2O9 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Nb40N21O16\\n\",\n        \"output\": \" Yes, Nb40N21O16 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ca2Si\\n\",\n        \"output\": \" No, Ca2Si is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CuPS3\\n\",\n        \"output\": \" No, CuPS3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Ga1Sb0.3As0.7\\n\",\n        \"output\": \" No, Ga1Sb0.3As0.7 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La2PI2\\n\",\n        \"output\": \" Yes, La2PI2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" SnS\\n\",\n        \"output\": \" No, SnS is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CaInAu\\n\",\n        \"output\": \" Yes, CaInAu is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Te0.4Se0.6\\n\",\n        \"output\": \" No, Te0.4Se0.6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li2TiMn3O8\\n\",\n        \"output\": \" Yes, Li2TiMn3O8 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Ba2ErGaTe5\\n\",\n        \"output\": \" No, Ba2ErGaTe5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" RbTiBr3\\n\",\n        \"output\": \" Yes, RbTiBr3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" La(SiOs)2\\n\",\n        \"output\": \" Yes, La(SiOs)2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" In3Au10\\n\",\n        \"output\": \" Yes, In3Au10 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" V2Si2O7\\n\",\n        \"output\": \" Yes, V2Si2O7 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" LiCl\\n\",\n        \"output\": \" No, LiCl is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" ScZn2\\n\",\n        \"output\": \" Yes, ScZn2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Li3Cr(NiO2)4\\n\",\n        \"output\": \" Yes, Li3Cr(NiO2)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" asia\\n\",\n        \"output\": \" asia is not a composition and it is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Tm2CdHg\\n\",\n        \"output\": \" Yes, Tm2CdHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" TlCr5Se3S5\\n\",\n        \"output\": \" No, TlCr5Se3S5 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Lu2InHg\\n\",\n        \"output\": \" Yes, Lu2InHg is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Er2Mg3Ru\\n\",\n        \"output\": \" Yes, Er2Mg3Ru is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Tb(FeP3)4\\n\",\n        \"output\": \" Yes, Tb(FeP3)4 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Ba3Bi0.5B1.5S6\\n\",\n        \"output\": \" No, Ba3Bi0.5B1.5S6 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Cs5Bi(PSe3)4\\n\",\n        \"output\": \" No, Cs5Bi(PSe3)4 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Y2ReB6\\n\",\n        \"output\": \" Yes, Y2ReB6 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" AgPd(IO3)3\\n\",\n        \"output\": \" No, AgPd(IO3)3 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" Al0.5Ga0.5As1\\n\",\n        \"output\": \" No, Al0.5Ga0.5As1 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" HfHg4(AsCl3)2\\n\",\n        \"output\": \" No, HfHg4(AsCl3)2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Cs2ZnGe3Se8\\n\",\n        \"output\": \" No, Cs2ZnGe3Se8 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" HoMn12\\n\",\n        \"output\": \" Yes, HoMn12 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" Yb4Sb3\\n\",\n        \"output\": \" Yes, Yb4Sb3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" ErRu3\\n\",\n        \"output\": \" Yes, ErRu3 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, is it metal? ->\",\n        \"input\": \" Mg3Ga7Co2\\n\",\n        \"output\": \" Yes, Mg3Ga7Co2 is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CdBr2\\n\",\n        \"output\": \" No, CdBr2 is not metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is composition metal? ->\",\n        \"input\": \" CoCu2Sn\\n\",\n        \"output\": \" Yes, CoCu2Sn is metal.\\n\"\n    },\n    {\n        \"instruction\": \"Is given composition metal? ->\",\n        \"input\": \" CeTl3\\n\",\n        \"output\": \" Yes, CeTl3 is metal.\\n\"\n    }\n]"
  },
  {
    "path": "dataset/matbench_steels/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 30,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('matbench_steels.csv')\\n\",\n    \"# key=csv column name, value=slot in Q\\n\",\n    \"slot = {\\\"composition\\\":\\\"composition\\\"}\\n\",\n    \"data_list = []\\n\",\n    \"for s in slot.keys():\\n\",\n    \"    for i, element in enumerate(df[s]):\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,2)\\n\",\n    \"\\n\",\n    \"        # What will be yield strength of composition at 800-1200 °C \\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What will be the yield strength of given composition at 800-1200 °C? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write a possible yield strength of given composition at 800-1200 °C. ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given composition, write its potential yield strength at 800-1200 °C. ->\\\"\\n\",\n    \"        answer = df['yield strength'][i]\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] = \\\" \\\"+ element +\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(answer)+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 31,\n   \"id\": \"166b1e11\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 32,\n   \"id\": \"52c48afe\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"312\\n\",\n      \"6\\n\",\n      \"10\\n\",\n      \"['Fe0.750C0.00184Mn0.000101Si0.000394Cr0.133Ni0.0814Mo0.0121V0.000109Nb0.0000596Co0.0000939Al0.0205', 'Fe0.755C0.00185Mn0.000101Si0.000198Cr0.134Ni0.0794Mo0.0127V0.000109Nb0.0000598Co0.0000942Al0.0158Ti0.000232', 'Fe0.671C0.000470Mn0.000514Si0.00100Cr0.000109Ni0.141Mo0.00882V0.000111Nb0.0000607Co0.147Al0.0159Ti0.0137', 'Fe0.682C0.00877Mn0.000202Si0.00967Cr0.134Ni0.00907Mo0.00861V0.00501Nb0.0000597Co0.142Al0.000616', 'Fe0.802C0.000468Mn0.000512Si0.00120Cr0.0526Ni0.111Mo0.0173V0.000110Nb0.0000605Co0.0000954Al0.0121Ti0.00258', 'Fe0.721C0.00970Mn0.000101Si0.0119Cr0.0875Ni0.0246Mo0.00752V0.00316Nb0.0000597Co0.134Al0.000617Ti0.000232']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"print(len(data_list))\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add_c = int(len(data_list)/50)\\n\",\n    \"add_n = int(len(data_list)/30)\\n\",\n    \"print(add_c)\\n\",\n    \"print(add_n)\\n\",\n    \"add_comps = random.sample(df['composition'].tolist(), add_c)\\n\",\n    \"print(add_comps)\\n\",\n    \"\\n\",\n    \"for an in add_comps:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    ran2 = random.sample(list(slot.values()), 1)[0]\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What is yield strength of composition? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write a possible yield strength of given composition. ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given composition, write its potential yield strength. ->\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] = \\\" \\\"+ an + \\\".\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" Unable to answer due to lack of conditions.\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 33,\n   \"id\": \"2b90dc97\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"318\\n\",\n      \"['beginner', 'downtown', 'pair', 'deodorant', 'hardhat', 'shell', 'wallet', 'david', 'samurai', 'black']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"print(len(data_list))\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add_nouns = random.sample(nouns, add_n)\\n\",\n    \"print(add_nouns[:10])\\n\",\n    \"for an in add_nouns:\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    ran1 = random.randint(0,2)\\n\",\n    \"    ran2 = random.sample(list(slot.values()), 1)[0]\\n\",\n    \"    if ran1 == 0:\\n\",\n    \"        question = \\\"What will be the yield strength of given composition at 800-1200 °C? ->\\\"\\n\",\n    \"    elif ran1 == 1:\\n\",\n    \"        question = \\\"Write a possible yield strength of given composition at 800-1200 °C. ->\\\"\\n\",\n    \"    elif ran1 == 2:\\n\",\n    \"        question = \\\"Given composition, write its potential yield strength at 800-1200 °C. ->\\\"\\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] = an\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" \\\"+an+\\\" is not a \\\"+ran2+\\\" and it does not have yield strength.\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\\n\",\n    \"random.shuffle(data_list)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 34,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('matbench_steels.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.8.0\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/matbench_steels/matbench_steels.csv",
    "content": "composition,yield strength\nFe0.620C0.000953Mn0.000521Si0.00102Cr0.000110Ni0.192Mo0.0176V0.000112Nb0.0000616Co0.146Al0.00318Ti0.0185,2411.5\nFe0.623C0.00854Mn0.000104Si0.000203Cr0.147Ni0.0000971Mo0.0179V0.00515N0.00163Nb0.0000614Co0.188W0.00729Al0.000845,1123.1\nFe0.625Mn0.000102Si0.000200Cr0.0936Ni0.129Mo0.00480V0.000110Nb0.0000604Co0.132Al0.00812Ti0.00669,1736.3\nFe0.634C0.000478Mn0.000523Si0.00102Cr0.000111Ni0.173Mo0.0237V0.000113Nb0.0000619Co0.146Al0.00277Ti0.0176,2487.3\nFe0.636C0.000474Mn0.000518Si0.00101Cr0.000109Ni0.188Mo0.00860V0.000112Nb0.0000612Co0.144Al0.00274Ti0.0184,2249.6\nFe0.636C0.00881Mn0.000203Si0.00972Cr0.135Ni0.00892Mo0.0114V0.000109Nb0.0000600Co0.190Al0.000620,1328.3\nFe0.644Mn0.000521Si0.00102Cr0.000110Ni0.177Mo0.0215V0.000112Nb0.0000617Co0.126Al0.00234Ti0.0269,2501.1\nFe0.646C0.00479Mn0.00597Si0.00492Cr0.135Ni0.0000980Mo0.0534V0.000113N0.000821Nb0.0000619Co0.148Al0.000640,1228.9\nFe0.648C0.000453Mn0.0000991Si0.0386Cr0.183Ni0.0195Mo0.000113V0.000107Nb0.0000586Co0.109Al0.000605Ti0.000569,1088.6\nFe0.648C0.00751Mn0.000103Si0.000201Cr0.158Ni0.0000961Mo0.0288V0.00531N0.00201Nb0.0000607Co0.149Al0.000836,1502.0\nFe0.650C0.000477Mn0.000522Si0.00102Cr0.000110Ni0.176Mo0.0215V0.000113Nb0.0000617Co0.126Al0.00170Ti0.0225,2411.5\nFe0.652Mn0.000522Si0.00102Cr0.000110Ni0.177Mo0.0209V0.000113Nb0.0000617Co0.126Al0.00212Ti0.0194,2331.1\nFe0.655C0.00752Mn0.000103Si0.000201Cr0.147Ni0.0000961Mo0.0276V0.00443N0.00161Nb0.0000607Co0.155Al0.000836,1274.7\nFe0.655Mn0.000522Si0.00102Cr0.000110Ni0.176Mo0.0215V0.00563Nb0.0000617Co0.117Al0.000425Ti0.0228,2402.3\nFe0.656C0.00758Mn0.000104Si0.000203Cr0.156Ni0.0000970Mo0.0424V0.00458N0.00122Nb0.0000613Co0.131Al0.000844,1460.7\nFe0.656C0.00930Mn0.000102Si0.000199Cr0.152Ni0.00875Mo0.0116V0.000110Nb0.000481Co0.161Al0.000621,1243.4\nFe0.657C0.000954Mn0.000522Si0.00102Cr0.000110Ni0.166Mo0.0243V0.00776Nb0.0000617Co0.120Al0.00340Ti0.0189,2381.6\nFe0.659C0.00747Mn0.000102Si0.0134Cr0.156Ni0.0000955Mo0.0297V0.00451N0.000800Nb0.0000603Co0.128Al0.000831,1412.5\nFe0.660C0.000484Mn0.000106Si0.000207Cr0.000112Ni0.148Mo0.0364V0.000114Nb0.0000625Co0.146Al0.000646Ti0.00752,1603.3\nFe0.661C0.000454Mn0.0000993Si0.0375Cr0.164Ni0.0381Mo0.000114V0.000107Nb0.0000587Co0.0972Al0.000606Ti0.000684,1185.1\nFe0.661C0.000475Mn0.000520Si0.00102Cr0.000110Ni0.170Mo0.0247V0.000112Nb0.0000615Co0.111Al0.0131Ti0.0177,2510.3\nFe0.662C0.000477Mn0.000521Si0.00102Cr0.000110Ni0.168Mo0.0236V0.000112Nb0.0000616Co0.119Al0.00488Ti0.0213,2372.4\nFe0.663C0.00329Mn0.000103Si0.000201Cr0.169Ni0.0000963Mo0.0294V0.00455N0.00121Nb0.0000608Co0.129Al0.000629,1312.6\nFe0.664C0.00751Mn0.00575Si0.000201Cr0.157Ni0.0000961Mo0.0301V0.00454N0.00121Nb0.0000607Co0.128Al0.00105,1350.4\nFe0.664C0.00754Mn0.000103Si0.000604Cr0.152Ni0.0105Mo0.0292V0.000111Nb0.00164Co0.134Al0.000629,1169.4\nFe0.664C0.00926Mn0.000101Si0.0101Cr0.134Ni0.00900Mo0.0114V0.000109Nb0.000479Co0.161Al0.000618,1322.1\nFe0.665C0.000468Mn0.000102Si0.000200Cr0.121Ni0.0768Mo0.0293V0.000110Nb0.0000606Co0.0823Al0.0254Ti0.000118,1870.6\nFe0.666C0.000482Mn0.000105Si0.000206Cr0.000111Ni0.149Mo0.0308V0.000114Nb0.0000623Co0.150Al0.000644Ti0.00242,1580.0\nFe0.666C0.00702Mn0.000102Si0.000200Cr0.157Ni0.0000958Mo0.0296V0.00508N0.00602Nb0.0000605Co0.129Al0.00104,1164.4\nFe0.666C0.00751Mn0.000103Si0.000201Cr0.155Ni0.0000960Mo0.0299V0.00963N0.00161Nb0.0000607Co0.129Al0.00104,1550.3\nFe0.667C0.000477Mn0.000522Si0.00102Cr0.000110Ni0.171Mo0.0233V0.000113Nb0.0000617Co0.115Al0.00361Ti0.0184,2381.6\nFe0.667C0.00984Mn0.000102Si0.000200Cr0.158Ni0.0000959Mo0.0295V0.00453N0.000804Nb0.0000606Co0.129Al0.00104,1405.6\nFe0.667C0.00984Mn0.000102Si0.000200Cr0.158Ni0.0000959Mo0.0295V0.00508N0.000804Nb0.0000606Co0.128Al0.00104,1529.6\nFe0.668C0.000469Mn0.000102Si0.000200Cr0.119Ni0.0764Mo0.0293V0.000110Nb0.0000606Co0.0817Al0.0252Ti0.000118,1825.8\nFe0.668C0.00972Mn0.00435Si0.00990Cr0.134Ni0.0112Mo0.0119V0.000109Nb0.0000598Co0.150Al0.000618,1352.2\nFe0.668Mn0.000102Si0.000200Cr0.119Ni0.0767Mo0.0292V0.000111Nb0.0000606Co0.0813Al0.0248Ti0.000235,1837.9\nFe0.669C0.00331Mn0.00590Si0.00648Cr0.129Ni0.0000969Mo0.0375V0.000112N0.00203Nb0.0000612Co0.147Al0.000632,1133.4\nFe0.669C0.00929Mn0.000102Si0.000596Cr0.151Ni0.0000950Mo0.0115V0.000110Nb0.000480Co0.157Al0.000620,1358.2\nFe0.669C0.00957Mn0.0000996Si0.0388Cr0.132Ni0.00876Mo0.0113V0.000107Nb0.000471Co0.129Al0.000608,1354.2\nFe0.670C0.00439Mn0.00704Si0.00563Cr0.138Ni0.0000999Mo0.000122V0.000115N0.00126Nb0.0000631Co0.147W0.0255Al0.000652,1081.1\nFe0.670C0.00564Mn0.000103Si0.000201Cr0.158Ni0.0000963Mo0.0300V0.00477N0.00121Nb0.0000608Co0.129Al0.000628,1515.8\nFe0.670C0.00798Mn0.000103Si0.000201Cr0.155Ni0.0000961Mo0.0299V0.00454N0.00121Nb0.0000607Co0.131Al0.000627,1502.0\nFe0.671C0.000470Mn0.000514Si0.00100Cr0.000109Ni0.141Mo0.00882V0.000111Nb0.0000607Co0.147Al0.0159Ti0.0137,2157.3\nFe0.671C0.00189Mn0.00569Si0.00547Cr0.134Ni0.0000969Mo0.0347V0.000112N0.00122Nb0.0000612Co0.145Al0.000632,1287.4\nFe0.671C0.00376Mn0.000103Si0.000201Cr0.157Ni0.0000962Mo0.0294V0.00510N0.00282Nb0.0000608Co0.130Al0.000628,1311.4\nFe0.671C0.00925Mn0.00516Si0.0103Cr0.135Ni0.00965Mo0.0115V0.000109Nb0.0000598Co0.147Al0.000618,1245.4\nFe0.672C0.00473Mn0.00527Si0.00647Cr0.131Ni0.0000968Mo0.0373V0.000111N0.00162Nb0.0000611Co0.141Al0.000631,1155.0\nFe0.672C0.00564Mn0.000103Si0.000201Cr0.156Ni0.0000962Mo0.0294V0.00454N0.00121Nb0.0000608Co0.129Al0.00105,1322.9\nFe0.673C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.144Mo0.0149V0.000112Nb0.0000614Co0.145Al0.000635Ti0.0215,1571.2\nFe0.673C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.180Mo0.0286V0.00482Nb0.0000614Co0.0842Al0.0201Ti0.00858,1288.4\nFe0.673C0.000908Mn0.0000992Si0.0361Cr0.167Ni0.0372Mo0.000114V0.000107Nb0.0000587Co0.0851Al0.000404Ti0.000569,1143.7\nFe0.674C0.00752Mn0.000103Si0.000201Cr0.156Ni0.0000961Mo0.0303V0.000111N0.00121Nb0.0000607Co0.129Al0.00146,1460.7\nFe0.674C0.00925Mn0.00516Si0.0101Cr0.135Ni0.00975Mo0.0115V0.000109Nb0.0000598Co0.145Al0.000618,1300.3\nFe0.674C0.0112Mn0.000102Si0.000199Cr0.0957Ni0.0829Mo0.00874V0.00307Nb0.0000602Co0.123Al0.000622Ti0.000234,1309.1\nFe0.675C0.00705Mn0.000103Si0.000201Cr0.157Ni0.0000962Mo0.0294V0.000111Nb0.0000608Co0.129Al0.00105,1338.0\nFe0.676C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.180Mo0.0279V0.000112Nb0.0000614Co0.0852Al0.0216Ti0.00846,1309.1\nFe0.677C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.146Mo0.0188V0.000113Nb0.0000617Co0.149Al0.000638Ti0.00839,1669.3\nFe0.677C0.00916Mn0.000100Si0.0294Cr0.134Ni0.00881Mo0.0113V0.000108Nb0.000474Co0.129Al0.000611,1382.2\nFe0.678C0.000464Mn0.000102Si0.000199Cr0.0873Ni0.114Mo0.000116V0.000110Nb0.0000600Co0.0992Al0.00806Ti0.0129,1768.0\nFe0.678C0.00421Mn0.00645Si0.00741Cr0.133Ni0.0000958Mo0.0233V0.000110N0.00161Nb0.0000605Co0.145Al0.000625,1131.9\nFe0.679C0.00705Mn0.000103Si0.000201Cr0.153Ni0.00135Mo0.0282V0.00233Nb0.0000608Co0.128Al0.000628,1341.7\nFe0.680Mn0.000102Si0.000199Cr0.127Ni0.0976Mo0.00856V0.000110Nb0.0000601Co0.0709Al0.00891Ti0.00654,1586.7\nFe0.680Mn0.000104Si0.000204Cr0.111Ni0.0680Mo0.0327V0.000112N0.000408Nb0.0000616Co0.106Al0.000636,1373.9\nFe0.681C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.181Mo0.0293V0.00439Nb0.0000618Co0.0847Al0.0108Ti0.00779,1164.4\nFe0.681C0.00744Mn0.000102Si0.000199Cr0.154Ni0.0000952Mo0.0175V0.0106N0.00120Nb0.0000601Co0.126Al0.00104,1240.2\nFe0.681C0.00877Mn0.00464Si0.00968Cr0.135Ni0.00898Mo0.00861V0.000109Nb0.0000597Co0.142Al0.000617,1250.8\nFe0.682C0.00515Mn0.000102Si0.000200Cr0.0995Ni0.0355Mo0.0117V0.00552Nb0.0000605Co0.159Al0.000625Ti0.000353,1453.8\nFe0.682C0.00877Mn0.000202Si0.00967Cr0.134Ni0.00907Mo0.00861V0.00501Nb0.0000597Co0.142Al0.000616,1241.0\nFe0.682C0.00925Mn0.000101Si0.0101Cr0.134Ni0.00899Mo0.0115V0.000109Nb0.000479Co0.143Al0.000618,1314.2\nFe0.683C0.00704Mn0.000103Si0.000201Cr0.156Ni0.0000961Mo0.0299V0.00454N0.00121Nb0.0000607Co0.117Al0.000836,1471.0\nFe0.683C0.00749Mn0.000102Si0.000200Cr0.156Ni0.0000958Mo0.0309V0.00453N0.00522Nb0.0000605Co0.112Al0.000834,1646.7\nFe0.683C0.00925Mn0.000202Si0.00969Cr0.134Ni0.00890Mo0.0114V0.000109Nb0.000120Co0.142Al0.000618,1258.6\nFe0.684C0.00699Mn0.000102Si0.000199Cr0.155Ni0.0000953Mo0.0177V0.00450N0.00120Nb0.0000602Co0.130Al0.000622,1233.3\nFe0.684C0.00795Mn0.000102Si0.000200Cr0.156Ni0.0000957Mo0.0306V0.00452N0.00481Nb0.0000604Co0.109Al0.00271,1536.5\nFe0.684C0.00920Mn0.000101Si0.0197Cr0.134Ni0.00885Mo0.0114V0.00228Nb0.000476Co0.129Al0.000614,1344.4\nFe0.685C0.00877Mn0.000101Si0.00967Cr0.134Ni0.00907Mo0.00855V0.00359Nb0.0000597Co0.141Al0.000617,1218.4\nFe0.685C0.0101Mn0.000101Si0.0199Cr0.134Ni0.00884Mo0.0114V0.000108Nb0.000475Co0.129Al0.000614,1383.7\nFe0.685C0.0112Mn0.000102Si0.000199Cr0.0957Ni0.0705Mo0.00991V0.00307Nb0.0000602Co0.123Al0.000622Ti0.000351,1550.3\nFe0.685C0.0116Mn0.000101Si0.000198Cr0.151Ni0.00882Mo0.0116V0.000109Nb0.000479Co0.131Al0.000619,1438.6\nFe0.686C0.000466Mn0.000102Si0.000199Cr0.0951Ni0.103Mo0.00694V0.00450Nb0.0000602Co0.0877Al0.00892Ti0.00666,1755.2\nFe0.686C0.000469Mn0.000410Si0.000802Cr0.107Ni0.0671Mo0.0161Co0.0767W0.00745Al0.0376,1680.6\nFe0.686C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.143Mo0.0185V0.000113Nb0.0000618Co0.150Al0.000638Ti0.00144,1267.1\nFe0.686C0.000910Mn0.0000995Si0.0354Cr0.146Ni0.0475Mo0.000114V0.000107Nb0.0000588Co0.0825Al0.000405Ti0.000457,1226.4\nFe0.687C0.000467Mn0.000102Si0.000200Cr0.0835Ni0.114Mo0.00573V0.000110Nb0.0000604Co0.0947Al0.00562Ti0.00832,1779.7\nFe0.687C0.00974Mn0.000101Si0.000198Cr0.151Ni0.00883Mo0.0116V0.000109Nb0.000480Co0.131Al0.000620,1372.9\nFe0.687C0.0162Mn0.000101Si0.000199Cr0.0965Ni0.0142Mo0.0116V0.00328Nb0.0000600Co0.170Al0.000620Ti0.000233,1731.7\nFe0.687Mn0.000102Si0.000199Cr0.119Ni0.0952Mo0.00716V0.000110Nb0.0000601Co0.0712W0.000851Al0.0118Ti0.00689,1729.4\nFe0.688C0.00877Mn0.000101Si0.00987Cr0.134Ni0.00898Mo0.00856V0.000109Nb0.0000597Co0.141Al0.000617,1311.1\nFe0.689C0.000476Mn0.000104Si0.000204Cr0.111Ni0.0683Mo0.0327V0.000112Nb0.0000615Co0.0975Al0.000636,1486.2\nFe0.689C0.00193Mn0.000105Si0.000206Cr0.000111Ni0.185Mo0.0362V0.000114Nb0.0000623Co0.0785Al0.00343Ti0.00507,1012.8\nFe0.690C0.00697Mn0.000102Si0.000199Cr0.150Ni0.00885Mo0.0116V0.000110Nb0.000481Co0.130Al0.000621,1278.2\nFe0.690C0.00785Mn0.000101Si0.0154Cr0.134Ni0.00898Mo0.0115V0.000109Nb0.000477Co0.132Al0.000617,1368.5\nFe0.690C0.00970Mn0.000101Si0.0111Cr0.134Ni0.00936Mo0.0114V0.00370Nb0.000478Co0.129Al0.000617,1280.7\nFe0.692C0.00837Mn0.00112Si0.00179Cr0.000107Ni0.169Mo0.000116V0.0474Nb0.0000601Co0.0764Al0.00228Ti0.000933,1605.4\nFe0.692C0.00968Mn0.000101Si0.0144Cr0.133Ni0.00887Mo0.0114V0.000109Nb0.000477Co0.130Al0.000616,1369.5\nFe0.693C0.000454Mn0.0000993Si0.0334Cr0.165Ni0.0381Mo0.000114V0.000107Nb0.0000587Co0.0685Al0.000405Ti0.000456,1205.8\nFe0.693C0.00877Mn0.000101Si0.0144Cr0.133Ni0.00897Mo0.0114V0.000109Nb0.000477Co0.130Al0.000616,1275.3\nFe0.694C0.0103Mn0.000102Si0.000200Cr0.0917Ni0.0440Mo0.00877V0.00308Nb0.0000604Co0.146W0.00153Al0.000624Ti0.000352,1575.5\nFe0.695C0.00971Mn0.000101Si0.00988Cr0.134Ni0.00889Mo0.0115V0.000109Nb0.000478Co0.130Al0.000617,1369.5\nFe0.695C0.0106Mn0.000101Si0.0103Cr0.133Ni0.00898Mo0.0114V0.000109Nb0.000478Co0.130Al0.000617,1359.7\nFe0.696C0.00143Mn0.000105Si0.000204Cr0.000110Ni0.180Mo0.0293V0.000113Nb0.0000618Co0.0682Al0.00319Ti0.0212,1233.3\nFe0.696C0.00878Mn0.000101Si0.00989Cr0.135Ni0.00927Mo0.0113V0.000109Nb0.000120Co0.129Al0.000617,1376.3\nFe0.696C0.00925Mn0.000101Si0.000198Cr0.148Ni0.0107Mo0.00573V0.000109Nb0.000538Co0.129Al0.000617,1376.7\nFe0.696C0.00974Mn0.000101Si0.000198Cr0.150Ni0.0000949Mo0.0116V0.000109Nb0.000480Co0.130Al0.000619,1348.9\nFe0.697C0.00972Mn0.000101Si0.00732Cr0.135Ni0.00909Mo0.0115V0.000109Nb0.000479Co0.130Al0.000618,1332.7\nFe0.699C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.166Mo0.0287V0.00383Nb0.0000618Co0.0847Al0.00829Ti0.00803,1287.3\nFe0.699C0.000946Mn0.000103Si0.000202Cr0.000109Ni0.140Mo0.00545V0.000112Nb0.0000612Co0.148Al0.000632Ti0.00487,1212.0\nFe0.700C0.000479Mn0.000523Si0.00102Cr0.000111Ni0.170Mo0.0298V0.000113Nb0.0000619Co0.0771Al0.00277Ti0.0180,2356.4\nFe0.700C0.00927Mn0.000101Si0.00594Cr0.133Ni0.00901Mo0.0114V0.000109Nb0.000479Co0.130Al0.000619,1299.8\nFe0.701C0.00750Mn0.000102Si0.000200Cr0.154Ni0.0000959Mo0.0289V0.00508N0.00121Nb0.0000606Co0.101Al0.000835,1405.6\nFe0.702C0.000943Mn0.000103Si0.000202Cr0.000109Ni0.142Mo0.000118V0.000111Nb0.0000609Co0.149Al0.000629Ti0.00509,1144.8\nFe0.702C0.00930Mn0.000102Si0.000199Cr0.133Ni0.0115Mo0.0117V0.000110Nb0.000481Co0.131Al0.000621,1423.8\nFe0.702Mn0.000102Si0.000200Cr0.154Ni0.0793Mo0.0152V0.000110Nb0.0000604Co0.0409Al0.00208Ti0.00574,1350.4\nFe0.702Mn0.000102Si0.000200Cr0.154Ni0.0802Mo0.0146V0.000110Nb0.0000604Co0.0409Al0.00249Ti0.00551,1274.7\nFe0.703C0.000908Mn0.0000992Si0.0375Cr0.146Ni0.0557Mo0.000114V0.000107Nb0.0000587Co0.0555Al0.000606Ti0.000569,1130.0\nFe0.703C0.00274Mn0.0209Si0.00625Cr0.173Ni0.0481Mo0.00864V0.000108Nb0.0000591Co0.0189Al0.0179,1237.0\nFe0.703C0.00883Mn0.000102Si0.000199Cr0.135Ni0.00942Mo0.0115V0.000110Nb0.000421Co0.131Al0.000621,1371.4\nFe0.703C0.00927Mn0.000101Si0.000198Cr0.128Ni0.0235Mo0.00574V0.000109Nb0.000599Co0.129Al0.000619,1273.3\nFe0.704C0.000476Mn0.000104Si0.000203Cr0.000110Ni0.148Mo0.0304V0.000112Nb0.0000615Co0.0892Al0.0191Ti0.00835,1393.5\nFe0.705C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.147Mo0.0304V0.000112Nb0.0000615Co0.0891Al0.0195Ti0.00835,1580.1\nFe0.706C0.000906Mn0.0000990Si0.0372Cr0.162Ni0.0361Mo0.000113V0.000107Nb0.0000586Co0.0554Al0.000806Ti0.000796,1109.3\nFe0.706C0.0106Mn0.000101Si0.00712Cr0.135Ni0.00899Mo0.0114V0.000109Nb0.000478Co0.120Al0.000617,1302.8\nFe0.706C0.0116Mn0.000101Si0.000199Cr0.0965Ni0.0589Mo0.00755V0.00317Nb0.0000600Co0.115Al0.000620Ti0.000349,1405.6\nFe0.707C0.000959Mn0.000105Si0.000205Cr0.000111Ni0.182Mo0.0306V0.000113Nb0.0000620Co0.0655Al0.00256Ti0.0107,1088.6\nFe0.707C0.000959Mn0.000105Si0.000205Cr0.000111Ni0.183Mo0.0306V0.000113Nb0.0000620Co0.0675Al0.00256Ti0.00770,1026.6\nFe0.707C0.0112Mn0.000102Si0.000199Cr0.0956Ni0.0485Mo0.00990V0.00318Nb0.0000601Co0.123Al0.000621Ti0.000350,1429.7\nFe0.709C0.0103Mn0.000102Si0.000200Cr0.0328Ni0.107Mo0.00692V0.000110Nb0.0000605Co0.133Al0.000625Ti0.000117,1810.0\nFe0.710C0.000477Mn0.000104Si0.000204Cr0.000110Ni0.149Mo0.0305V0.000112Nb0.0000617Co0.0885Al0.0127Ti0.00814,1123.1\nFe0.711C0.00699Mn0.000102Si0.000199Cr0.0969Ni0.0458Mo0.00875V0.00549Nb0.0000603Co0.123Al0.000622Ti0.000234,1412.5\nFe0.711C0.00931Mn0.000102Si0.000199Cr0.113Ni0.0237Mo0.0115V0.000110Nb0.000602Co0.130Al0.000622,1282.2\nFe0.711C0.0108Mn0.000102Si0.000200Cr0.0336Ni0.108Mo0.00697V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000117,1777.6\nFe0.712C0.00143Mn0.000104Si0.000203Cr0.000110Ni0.146Mo0.0297V0.000112Nb0.00123Co0.0852Al0.0207Ti0.00310,1026.6\nFe0.712C0.00144Mn0.000105Si0.000205Cr0.000111Ni0.180Mo0.0306V0.000113Nb0.0000620Co0.0655Al0.00235Ti0.00842,1109.3\nFe0.712C0.00471Mn0.00639Si0.00746Cr0.133Ni0.0000964Mo0.0363V0.000111N0.00121Nb0.0000609Co0.0980Al0.000629,1258.2\nFe0.712C0.0103Mn0.000102Si0.000200Cr0.0336Ni0.108Mo0.00698V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000117,1743.5\nFe0.713C0.00984Mn0.000102Si0.000200Cr0.0335Ni0.107Mo0.00698V0.000110Nb0.0000606Co0.129Al0.000209Ti0.000118,1792.1\nFe0.713C0.0108Mn0.000102Si0.000200Cr0.0335Ni0.106Mo0.00697V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000117,1741.8\nFe0.713C0.0108Mn0.000102Si0.000200Cr0.0336Ni0.107Mo0.00691V0.000110Nb0.0000605Co0.128Al0.000208Ti0.000117,1746.6\nFe0.713C0.0112Mn0.000102Si0.000200Cr0.0337Ni0.106Mo0.00697V0.000110Nb0.0000605Co0.128Al0.000208Ti0.000117,1804.2\nFe0.714C0.00138Mn0.00602Si0.00589Cr0.154Ni0.0798Mo0.0144V0.000108Nb0.0000593Co0.0000935Al0.0245,1478.4\nFe0.714C0.00984Mn0.000102Si0.000200Cr0.0336Ni0.106Mo0.00698V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000118,1795.5\nFe0.714C0.0108Mn0.000102Si0.000400Cr0.0337Ni0.106Mo0.00703V0.000110Nb0.0000605Co0.128Al0.000208Ti0.000117,1818.0\nFe0.715C0.00378Mn0.00609Si0.00605Cr0.133Ni0.0000966Mo0.0372V0.000111N0.00202Nb0.0000610Co0.0962Al0.000630,1287.4\nFe0.717C0.000960Mn0.000105Si0.000205Cr0.000111Ni0.178Mo0.0288V0.000113Nb0.00186Co0.0665Al0.00192Ti0.00494,1005.9\nFe0.718C0.000473Mn0.000103Si0.000606Cr0.0866Ni0.0969Mo0.00118N0.000405Co0.0784W0.00707Al0.00421Ti0.00581,1525.0\nFe0.718C0.00317Mn0.00594Si0.00581Cr0.178Ni0.0648Mo0.000113V0.000107Nb0.0000585Co0.0000922Al0.0242,1362.9\nFe0.719C0.000945Mn0.000103Si0.000202Cr0.0557Ni0.108Mo0.0302V0.000111Nb0.0000611Co0.0597Al0.0149Ti0.0111,1071.4\nFe0.720C0.000948Mn0.000104Si0.000203Cr0.0559Ni0.109Mo0.0303V0.00548Nb0.0000613Co0.0609Al0.00865Ti0.00880,1136.8\nFe0.720C0.00407Mn0.0277Si0.00619Cr0.183Ni0.0411Mo0.000113V0.000107Nb0.0000585Co0.0000923Al0.0181,1236.6\nFe0.721C0.000476Mn0.000104Si0.000203Cr0.0560Ni0.109Mo0.0304V0.0105Nb0.0000615Co0.0611Al0.00191Ti0.00931,1040.4\nFe0.721C0.000955Mn0.000104Si0.000204Cr0.000110Ni0.143Mo0.0299V0.00484Nb0.00124Co0.0867Al0.0102Ti0.00240,1026.6\nFe0.721C0.000955Mn0.000104Si0.000204Cr0.000110Ni0.146Mo0.0287V0.00293Nb0.0000617Co0.0846Al0.00765Ti0.00850,1164.4\nFe0.721C0.00189Mn0.00455Si0.00647Cr0.131Ni0.0000967Mo0.0364V0.000111N0.00122Nb0.0000611Co0.0963Al0.000631,1219.7\nFe0.721C0.00191Mn0.000104Si0.000204Cr0.000110Ni0.147Mo0.0299V0.000113Nb0.00123Co0.0856Al0.0106Ti0.00288,1019.7\nFe0.721C0.00970Mn0.000101Si0.0119Cr0.0875Ni0.0246Mo0.00752V0.00316Nb0.0000597Co0.134Al0.000617Ti0.000232,1391.8\nFe0.722C0.000475Mn0.000104Si0.000203Cr0.0549Ni0.109Mo0.0297V0.000112Nb0.0000614Co0.0600Al0.00190Ti0.0216,1164.4\nFe0.722C0.00797Mn0.00164Si0.00100Cr0.0322Ni0.0961Mo0.00710V0.000111Nb0.0000606Co0.131Al0.000209,1547.3\nFe0.723C0.00320Mn0.00600Si0.00587Cr0.158Ni0.0655Mo0.0129V0.000108Nb0.0000591Co0.0000932Al0.0244,1463.0\nFe0.724C0.00140Mn0.000510Si0.00339Cr0.000108Ni0.157Mo0.000117V0.0440Nb0.0000603Co0.0656Al0.00208Ti0.00164,1536.5\nFe0.725C0.0155Mn0.000677Si0.0899Cr0.000102Ni0.167Mo0.000111V0.000104Nb0.0000572Co0.0000902Al0.000591,1250.5\nFe0.727C0.000476Mn0.000104Si0.000203Cr0.0549Ni0.108Mo0.0304V0.000112Nb0.0000615Co0.0611Al0.00212Ti0.0154,1123.1\nFe0.730C0.00414Mn0.0101Si0.00983Cr0.186Ni0.0395Mo0.0158V0.000108N0.00394Nb0.0000594Co0.0000937Al0.000614,1016.4\nFe0.731C0.00897Mn0.000103Si0.000202Cr0.0742Ni0.0271Mo0.0142V0.00312Nb0.0000610Co0.137W0.00401Al0.000631Ti0.000237,1371.1\nFe0.732C0.00415Mn0.00504Si0.00553Cr0.182Ni0.0395Mo0.0117V0.000109Nb0.0000597Co0.0190Al0.000616,1117.3\nFe0.732C0.00480Mn0.00556Si0.00533Cr0.136Ni0.0000981Mo0.000120V0.000113N0.00123Nb0.0000620Co0.0953W0.0188Al0.000640,1232.0\nFe0.733C0.00750Mn0.00164Si0.00100Cr0.0213Ni0.0964Mo0.00587V0.000111Nb0.0000606Co0.133Al0.000209,1592.9\nFe0.734C0.00750Mn0.000615Si0.000802Cr0.0211Ni0.0974Mo0.00575V0.000111Nb0.0000606Co0.132Al0.000209Ti0.000118,1629.9\nFe0.735C0.000951Mn0.000104Si0.000203Cr0.0549Ni0.108Mo0.0286V0.000112Nb0.0000615Co0.0601Al0.00190Ti0.00978,1047.3\nFe0.735C0.00514Mn0.00593Si0.00440Cr0.128Ni0.0000957Mo0.0227V0.000110N0.000802Nb0.0000604Co0.0972Al0.000624,1096.5\nFe0.735C0.0111Mn0.000101Si0.000198Cr0.0974Ni0.0266Mo0.00754V0.00404Nb0.0000599Co0.117Al0.000619Ti0.000349,1615.8\nFe0.736C0.0107Mn0.000101Si0.000198Cr0.0964Ni0.0266Mo0.00755V0.00328Nb0.0000600Co0.118Al0.000619Ti0.000349,1522.7\nFe0.737C0.000956Mn0.000105Si0.000204Cr0.000110Ni0.127Mo0.0299V0.00530Nb0.0000618Co0.0867Al0.00426Ti0.00852,1061.1\nFe0.737C0.00836Mn0.000102Si0.000199Cr0.0977Ni0.0266Mo0.00756V0.00318Nb0.0000601Co0.118Al0.000621Ti0.000350,1426.2\nFe0.737C0.0111Mn0.000101Si0.000198Cr0.0964Ni0.0266Mo0.00755V0.00317Nb0.0000599Co0.117Al0.000619Ti0.000233,1564.0\nFe0.740C0.00457Mn0.0300Si0.00586Cr0.179Ni0.0393Mo0.000114V0.000108Nb0.0000591Co0.0000931Al0.000610,1130.4\nFe0.741C0.00702Mn0.00164Si0.00100Cr0.0321Ni0.0964Mo0.00586V0.000110Nb0.0000605Co0.115Al0.000208,1455.4\nFe0.744C0.00414Mn0.0217Si0.00354Cr0.180Ni0.0401Mo0.00598V0.000108Nb0.0000594Co0.0000937Al0.000614,1028.7\nFe0.745C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0794Mo0.0129V0.000108Nb0.0000594Co0.0000937Al0.0268Ti0.000115,1521.3\nFe0.747C0.000899Mn0.000982Si0.0820Cr0.000104Ni0.166Mo0.000112V0.000106Nb0.0000581Co0.0000916Al0.00140Ti0.00101,1801.8\nFe0.748C0.00704Mn0.00164Si0.00120Cr0.0218Ni0.0967Mo0.00716V0.000111Nb0.0000606Co0.116Al0.000209,1503.4\nFe0.750C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0789Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0218Ti0.00104,1350.3\nFe0.750C0.00184Mn0.000101Si0.000394Cr0.133Ni0.0814Mo0.0121V0.000109Nb0.0000596Co0.0000939Al0.0205,1308.0\nFe0.751C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0128V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0217Ti0.00104,1357.9\nFe0.751C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0128V0.000109Nb0.0000596Co0.0000939Al0.0220Ti0.000578,1317.0\nFe0.751C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0787Mo0.0128V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0217Ti0.000231,1269.0\nFe0.751C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0782Mo0.0128V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0215Ti0.000116,1306.9\nFe0.751C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0791Mo0.0129V0.000109Nb0.0000596Co0.0000940Al0.0211Ti0.000116,1285.0\nFe0.751C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0783Mo0.0129V0.000109Nb0.0000596Co0.0000939Al0.0220Ti0.000116,1297.5\nFe0.751C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0785Mo0.0128V0.000109Nb0.0000596Co0.0000939Al0.0217Ti0.000578,1344.0\nFe0.751C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0786Mo0.0127V0.000109Nb0.0000596Co0.0000939Al0.0213Ti0.00116,1348.6\nFe0.751C0.00563Mn0.00185Si0.00120Cr0.0218Ni0.0967Mo0.00587V0.000111Nb0.0000606Co0.116Al0.000209,1463.3\nFe0.752C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0781Mo0.0127V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0215Ti0.000578,1276.7\nFe0.752C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0218Ti0.000231,1296.0\nFe0.752C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0784Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0209Ti0.000116,1277.7\nFe0.752C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0783Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0209Ti0.00104,1391.2\nFe0.752C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0787Mo0.0129V0.000109Nb0.0000596Co0.0000940Al0.0213Ti0.000116,1312.0\nFe0.753C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0127V0.000109Nb0.0000596Co0.0000940Al0.0211Ti0.000231,1276.5\nFe0.753C0.00929Mn0.000102Si0.000199Cr0.0880Ni0.0200Mo0.00756V0.00318Nb0.0000600Co0.117Al0.000620Ti0.000233,1357.3\nFe0.754C0.00184Mn0.000101Si0.000197Cr0.132Ni0.0780Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0213Ti0.000347,1294.9\nFe0.754C0.00599Mn0.0101Si0.00493Cr0.165Ni0.0396Mo0.0159V0.000109N0.00395Nb0.0000596Co0.0000940Al0.000616,1155.0\nFe0.754C0.00640Mn0.0300Si0.00469Cr0.166Ni0.0387Mo0.000114V0.000108Nb0.0000591Co0.0000931Al0.000610,1153.4\nFe0.755C0.00185Mn0.000101Si0.000198Cr0.134Ni0.0794Mo0.0127V0.000109Nb0.0000598Co0.0000942Al0.0158Ti0.000232,1280.2\nFe0.755C0.00552Mn0.00543Si0.0236Cr0.128Ni0.0188Mo0.0173V0.00380N0.00197Nb0.00244Co0.0375Al0.000615,1074.9\nFe0.757C0.000465Mn0.000712Si0.00219Cr0.121Ni0.0981Mo0.0119V0.000110Nb0.0000602Co0.0000948Al0.00497Ti0.00269,1157.5\nFe0.757C0.00185Mn0.000101Si0.000791Cr0.133Ni0.0781Mo0.0127V0.000109Nb0.0000597Co0.0000942Al0.0158Ti0.000232,1280.8\nFe0.757C0.0186Mn0.00163Si0.000199Cr0.131Ni0.0000953Mo0.0341V0.0105Nb0.0000602Co0.0467Al0.000622,1667.4\nFe0.758C0.00142Mn0.000104Si0.000203Cr0.123Ni0.0932Mo0.000119V0.000112Nb0.0000612Co0.0000965W0.0124Al0.00822Ti0.00309,1199.0\nFe0.758C0.00185Mn0.000101Si0.000198Cr0.132Ni0.0780Mo0.0127V0.000109Nb0.0000597Co0.0000942Al0.0167Ti0.000348,1305.4\nFe0.759C0.000472Mn0.000103Si0.000202Cr0.000109Ni0.203Mo0.0124V0.000111Nb0.0000610Co0.0000961Al0.00273Ti0.0225,1661.2\nFe0.760C0.000454Mn0.000992Si0.0640Cr0.000105Ni0.172Mo0.000114V0.000107Nb0.0000587Co0.0000925Al0.00101Ti0.00125,1474.4\nFe0.760C0.000468Mn0.000102Si0.000200Cr0.113Ni0.0986Mo0.0181V0.000110Nb0.0000605Co0.0000953Al0.00749Ti0.00129,1091.4\nFe0.762C0.000930Mn0.00752Si0.00199Cr0.110Ni0.0971Mo0.0115V0.000110Nb0.0000601Co0.0000948Al0.00621Ti0.00257,1145.8\nFe0.763C0.000466Mn0.000509Si0.000398Cr0.114Ni0.101Mo0.0120V0.000110Nb0.0000602Co0.0000949Al0.00746Ti0.000935,1194.0\nFe0.763C0.00479Mn0.00524Si0.00615Cr0.133Ni0.0196Mo0.000120V0.000113Nb0.0000619Co0.0488W0.0188Al0.000640,1235.9\nFe0.763Mn0.00102Si0.00814Cr0.109Ni0.0988Mo0.0116V0.000109Nb0.0000600Co0.0000946Al0.00517Ti0.00268,1221.6\nFe0.764C0.000467Mn0.000511Si0.00200Cr0.0831Ni0.117Mo0.0178V0.000110Nb0.0000604Co0.0000952Al0.0131Ti0.00234,1506.8\nFe0.765C0.000909Mn0.00109Si0.0618Cr0.000105Ni0.170Mo0.000114V0.000107Nb0.0000587Co0.0000926Al0.000607,1419.4\nFe0.765Mn0.000713Si0.00199Cr0.112Ni0.0992Mo0.0128V0.000110Nb0.0000603Co0.0000950Al0.00519Ti0.00281,1224.7\nFe0.765Mn0.00112Si0.00597Cr0.110Ni0.0990Mo0.0119V0.000110Nb0.0000601Co0.0000948Al0.00414Ti0.00257,1173.8\nFe0.766C0.000468Mn0.000819Si0.00100Cr0.102Ni0.103Mo0.0188V0.000110Nb0.0000606Co0.0000955Al0.00563Ti0.00259,1267.8\nFe0.766C0.00140Mn0.000102Si0.000199Cr0.115Ni0.0900Mo0.0143V0.000110Nb0.0000601Co0.0000948Al0.00952Ti0.00327,1182.0\nFe0.766Mn0.000510Si0.000399Cr0.121Ni0.0945Mo0.0120V0.000110Nb0.0000603Co0.0000950Al0.00270Ti0.00351,1172.0\nFe0.766Mn0.00366Si0.00159Cr0.110Ni0.0981Mo0.0118V0.000110Nb0.0000602Co0.0000949Al0.00622Ti0.00269,1178.9\nFe0.766Mn0.00448Si0.00159Cr0.109Ni0.0981Mo0.0117V0.000110Nb0.0000602Co0.0000949Al0.00622Ti0.00257,1163.0\nFe0.767C0.000465Mn0.00112Si0.00358Cr0.110Ni0.0981Mo0.0119V0.000110Nb0.0000601Co0.0000948Al0.00559Ti0.00257,1175.4\nFe0.768C0.000466Mn0.000306Si0.000598Cr0.110Ni0.100Mo0.0128V0.000110Nb0.0000603Co0.0000951Al0.00478Ti0.00281,1340.8\nFe0.768C0.000466Mn0.00122Si0.00119Cr0.111Ni0.0972Mo0.0119V0.000110Nb0.0000602Co0.0000949Al0.00642Ti0.00245,1258.8\nFe0.768C0.000468Mn0.000512Si0.00180Cr0.0827Ni0.117Mo0.0179V0.000110Nb0.0000605Co0.0000954Al0.00958Ti0.00235,1414.5\nFe0.768C0.000931Mn0.00244Si0.00199Cr0.110Ni0.0981Mo0.0113V0.000110Nb0.0000602Co0.0000948Al0.00497Ti0.00269,1167.2\nFe0.769Mn0.000509Si0.000398Cr0.112Ni0.0953Mo0.0119V0.000110Nb0.0000602Co0.0000949Al0.00725Ti0.00362,1282.2\nFe0.770C0.000470Mn0.000103Si0.000201Cr0.000109Ni0.168Mo0.0124V0.0222Nb0.0000607Co0.0000957Al0.00251Ti0.0236,1998.6\nFe0.770C0.000930Mn0.00488Si0.00199Cr0.107Ni0.0952Mo0.0112V0.000110Nb0.0000601Co0.0000948Al0.00600Ti0.00245,1188.6\nFe0.770Mn0.000509Si0.000398Cr0.111Ni0.0972Mo0.0120V0.000110Nb0.0000602Co0.0000949Al0.00726Ti0.00199,1243.0\nFe0.771Mn0.00122Si0.00140Cr0.107Ni0.100Mo0.0123V0.000110Nb0.0000603Co0.0000950Al0.00477Ti0.00257,1150.6\nFe0.772C0.0169Mn0.00226Si0.000201Cr0.0732Ni0.0000961Mo0.0338V0.0106Nb0.0000607Co0.0905Al0.000627,1846.5\nFe0.773C0.000933Mn0.000612Si0.00259Cr0.112Ni0.0945Mo0.0126V0.000110Nb0.0000603Co0.0000950Al0.00187Ti0.00152,1005.9\nFe0.773C0.00141Mn0.000512Si0.00220Cr0.0812Ni0.116Mo0.0179V0.000110Nb0.0000606Co0.0000955Al0.00522Ti0.00235,1218.8\nFe0.774Mn0.000511Si0.000599Cr0.111Ni0.0985Mo0.0120V0.000110Nb0.0000604Co0.0000952Al0.00187Ti0.00105,1032.1\nFe0.777C0.000470Mn0.000719Si0.00201Cr0.0836Ni0.115Mo0.0178V0.000111Nb0.0000607Co0.0000958Al0.00167Ti0.000707,1010.8\nFe0.777C0.00140Mn0.000102Si0.000199Cr0.122Ni0.0824Mo0.000117V0.000110Nb0.0000603Co0.0000950W0.00561Al0.00810Ti0.00316,1194.0\nFe0.778C0.000465Mn0.000813Si0.00238Cr0.0966Ni0.0808Mo0.0189V0.000110Nb0.0000601Co0.0000947Al0.0186Ti0.00268,1462.7\nFe0.778C0.000931Mn0.000611Si0.00159Cr0.0796Ni0.0981Mo0.0189V0.000110Nb0.0000602Co0.0000949Al0.0189Ti0.00269,1555.8\nFe0.778Mn0.00122Si0.00159Cr0.112Ni0.0876Mo0.0115V0.000110Nb0.0000602Co0.0000949Al0.00539Ti0.00245,1207.8\nFe0.779C0.000946Mn0.000103Si0.000202Cr0.000109Ni0.173Mo0.0184V0.0100Nb0.0000611Co0.0000964Al0.00147Ti0.0166,1730.2\nFe0.779C0.00139Mn0.000101Si0.000198Cr0.114Ni0.0973Mo0.000116V0.000109Nb0.0000597Co0.0000941Al0.00432Ti0.00359,1125.0\nFe0.779C0.00141Mn0.000103Si0.000201Cr0.000109Ni0.174Mo0.0130V0.000111Nb0.0000608Co0.0000959Al0.00209Ti0.0295,2006.0\nFe0.779C0.00141Mn0.000103Si0.000201Cr0.000109Ni0.174Mo0.0130V0.000111Nb0.0000608Co0.0000959Al0.00230Ti0.0295,2005.5\nFe0.780C0.000457Mn0.000599Si0.0504Cr0.000106Ni0.166Mo0.000114V0.000108Nb0.0000591Co0.0000931Al0.00102Ti0.000802,1309.1\nFe0.780C0.000465Mn0.00122Si0.00159Cr0.105Ni0.0953Mo0.00991V0.000110Nb0.0000602Co0.0000949Al0.00414Ti0.00222,1087.0\nFe0.780C0.000467Mn0.000510Si0.00200Cr0.0830Ni0.0993Mo0.0179V0.000110Nb0.0000603Co0.0000951Al0.0139Ti0.00234,1475.8\nFe0.781C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.173Mo0.0184V0.0112Nb0.0000613Co0.0000967W0.00102Al0.00106Ti0.0131,1688.1\nFe0.781C0.00141Mn0.000103Si0.000201Cr0.000109Ni0.167Mo0.000118V0.0200Nb0.0152Co0.0000960Al0.00210Ti0.0126,1730.2\nFe0.782C0.0181Mn0.00187Si0.000203Cr0.0816Ni0.0000973Mo0.0576V0.0108Nb0.0000615Co0.0476Al0.000635,1577.8\nFe0.783C0.0187Mn0.00184Si0.000200Cr0.104Ni0.0000955Mo0.0341V0.0106Nb0.0000603Co0.0463Al0.000623,1798.3\nFe0.784C0.000919Mn0.00100Si0.0397Cr0.000106Ni0.173Mo0.000115V0.000108Nb0.0000594Co0.0000936Al0.000614,1298.8\nFe0.785C0.000467Mn0.000511Si0.00180Cr0.0820Ni0.0985Mo0.0178V0.000110Nb0.0000604Co0.0000952Al0.0108Ti0.00235,1383.5\nFe0.785C0.000931Mn0.000102Si0.000199Cr0.000108Ni0.167Mo0.000117V0.0209Nb0.0000602Co0.0000949Al0.00187Ti0.0241,1730.2\nFe0.786C0.000469Mn0.000512Si0.00120Cr0.0576Ni0.124Mo0.0172V0.000110Nb0.0000606Co0.0000955Al0.0106Ti0.00235,1404.2\nFe0.786C0.000473Mn0.000310Si0.000202Cr0.000109Ni0.175Mo0.0182V0.000112Nb0.0000612Co0.0000965Al0.00190Ti0.0167,1641.2\nFe0.787C0.000474Mn0.000207Si0.000203Cr0.000109Ni0.176Mo0.0181V0.000112Nb0.0000612Co0.0000965Al0.00190Ti0.0150,1599.4\nFe0.787C0.0137Mn0.000103Si0.000202Cr0.0111Ni0.101Mo0.0118V0.00111Nb0.0000610Co0.0689W0.00394Al0.000630Ti0.000118,1683.0\nFe0.788Mn0.000104Si0.000203Cr0.000109Ni0.176Mo0.0184V0.000112Nb0.0000613Co0.0000966Al0.00105Ti0.0166,1716.3\nFe0.789C0.00143Mn0.000104Si0.000204Cr0.000110Ni0.181Mo0.000119V0.000112Nb0.0000617Co0.0000972W0.00935Al0.00212Ti0.0168,1600.0\nFe0.789Mn0.000719Si0.00161Cr0.0814Ni0.101Mo0.0194V0.000111Nb0.0000607Co0.0000957Al0.00439Ti0.00271,1263.6\nFe0.792C0.000470Mn0.000411Si0.00201Cr0.0862Ni0.0980Mo0.0181V0.000111Nb0.0000607Co0.0000957Al0.00167Ti0.000589,1061.7\nFe0.793C0.000468Mn0.000819Si0.00240Cr0.0962Ni0.0800Mo0.0190V0.000110Nb0.0000605Co0.0000954Al0.00521Ti0.00235,1169.2\nFe0.794C0.000470Mn0.000617Si0.00101Cr0.0847Ni0.0981Mo0.0188V0.000111Nb0.0000608Co0.0000958Al0.00126Ti0.00118,1036.9\nFe0.795C0.00141Mn0.000717Si0.000801Cr0.0963Ni0.0810Mo0.0191V0.000110Nb0.0000606Co0.0000955Al0.00313Ti0.00270,1150.6\nFe0.796C0.000469Mn0.000103Si0.000201Cr0.000108Ni0.174Mo0.00587V0.000111Nb0.0000606Co0.0000956Al0.00167Ti0.0212,1737.2\nFe0.797C0.000939Mn0.00215Si0.00381Cr0.0540Ni0.118Mo0.0175V0.000111Nb0.0000607Co0.0000957Al0.00481Ti0.00165,1194.0\nFe0.798C0.000469Mn0.000820Si0.00100Cr0.0504Ni0.116Mo0.0184V0.000111Nb0.0000606Co0.0000955Al0.0119Ti0.00235,1390.4\nFe0.799C0.000468Mn0.0256Si0.000401Cr0.000108Ni0.173Mo0.000117V0.000110Nb0.0000605Co0.0000955Al0.00104Ti0.000470,1471.1\nFe0.799C0.000469Mn0.000513Si0.00241Cr0.0520Ni0.117Mo0.0176V0.000111Nb0.0000606Co0.0000956Al0.00835Ti0.00224,1272.6\nFe0.799C0.000470Mn0.000103Si0.000201Cr0.000108Ni0.167Mo0.00847V0.000111Nb0.0000607Co0.0000957Al0.00167Ti0.0224,1392.4\nFe0.799C0.000471Mn0.000103Si0.000201Cr0.000109Ni0.165Mo0.0118V0.000111Nb0.0000609Co0.0000960Al0.00147Ti0.0215,1874.6\nFe0.799C0.000936Mn0.000102Si0.000200Cr0.000108Ni0.170Mo0.00375V0.000110Nb0.0000605Co0.0000954Al0.00167Ti0.0238,1730.2\nFe0.800C0.000470Mn0.000616Si0.000602Cr0.0506Ni0.117Mo0.0186V0.000111Nb0.0000607Co0.0000957Al0.00982Ti0.00224,1390.4\nFe0.801C0.000469Mn0.00103Si0.00361Cr0.0528Ni0.116Mo0.0175V0.000111Nb0.0000607Co0.0000957Al0.00522Ti0.00177,1230.6\nFe0.801C0.000470Mn0.000205Si0.000603Cr0.0543Ni0.117Mo0.0176V0.000111Nb0.0000607Co0.0000958Al0.00648Ti0.00248,1309.8\nFe0.801C0.000934Mn0.000102Si0.000200Cr0.000108Ni0.171Mo0.00175V0.000110Nb0.0000604Co0.0000952Al0.00208Ti0.0229,1674.6\nFe0.801C0.000939Mn0.000821Si0.000803Cr0.0513Ni0.116Mo0.0185V0.000111Nb0.0000607Co0.0000957Al0.00794Ti0.00271,1243.6\nFe0.802C0.000468Mn0.000512Si0.00120Cr0.0526Ni0.111Mo0.0173V0.000110Nb0.0000605Co0.0000954Al0.0121Ti0.00258,1437.3\nFe0.802C0.000470Mn0.000308Si0.00221Cr0.0518Ni0.117Mo0.0178V0.000111Nb0.0000607Co0.0000958Al0.00544Ti0.00236,1216.8\nFe0.802C0.0174Mn0.00185Si0.000201Cr0.0805Ni0.0000962Mo0.0403V0.0106Nb0.0000608Co0.0468Al0.000628,1784.5\nFe0.802Mn0.000410Si0.00120Cr0.0543Ni0.114Mo0.0175V0.000111Nb0.0000607Co0.0000957Al0.00815Ti0.00236,1324.3\nFe0.803C0.000460Mn0.000402Si0.0368Cr0.000106Ni0.157Mo0.000115V0.000108Nb0.0000594Co0.0000937Al0.00102Ti0.000923,1188.5\nFe0.803C0.000470Mn0.000823Si0.000805Cr0.0511Ni0.117Mo0.0184V0.000111Nb0.0000608Co0.0000959Al0.00544Ti0.00224,1212.6\nFe0.803C0.0168Mn0.00215Si0.000200Cr0.0834Ni0.0000957Mo0.0334V0.0127Nb0.0000605Co0.0470Al0.000625,1819.0\nFe0.803C0.0174Mn0.00236Si0.000201Cr0.0779Ni0.0000960Mo0.0335V0.0122Nb0.00473Co0.0477Al0.000627,1340.1\nFe0.803Mn0.000512Si0.00120Cr0.0520Ni0.110Mo0.0173V0.000110Nb0.0000605Co0.0000954Al0.0137Ti0.00235,1451.7\nFe0.804C0.0166Mn0.00238Si0.000202Cr0.0782Ni0.0000969Mo0.0343V0.0114Nb0.0000612Co0.0473W0.00476Al0.000632,1688.1\nFe0.805C0.000470Mn0.000719Si0.000804Cr0.0496Ni0.116Mo0.0184V0.000111Nb0.0000608Co0.0000958Al0.00711Ti0.00212,1254.0\nFe0.806C0.000468Mn0.0176Si0.000401Cr0.000108Ni0.174Mo0.000117V0.000110Nb0.0000606Co0.0000955Al0.00104Ti0.000705,1136.9\nFe0.806C0.0176Mn0.00181Si0.000209Cr0.0802Ni0.0000999Mo0.00153V0.0124Nb0.0000631Co0.0501W0.0293Al0.000652,1681.2\nFe0.807C0.000470Mn0.000513Si0.00221Cr0.0501Ni0.116Mo0.0164V0.000111Nb0.0000607Co0.0000957Al0.00439Ti0.00236,1167.2\nFe0.808C0.0201Mn0.00214Si0.000200Cr0.0770Ni0.0000955Mo0.0328V0.0112Nb0.0000603Co0.0475Al0.000623,1736.3\nFe0.810C0.000940Mn0.000103Si0.000201Cr0.000109Ni0.151Mo0.0118V0.000111Nb0.0000608Co0.0000958Al0.00209Ti0.0234,1723.2\nFe0.811C0.0182Mn0.00225Si0.000200Cr0.0755Ni0.0000957Mo0.0337V0.0119Nb0.0000605Co0.0467Al0.000625,1688.1\nFe0.812C0.000934Mn0.000715Si0.00220Cr0.0507Ni0.0975Mo0.0181V0.000110Nb0.0000604Co0.0000952Al0.0146Ti0.00258,1420.0\nFe0.813C0.0187Mn0.00143Si0.000200Cr0.0800Ni0.0000957Mo0.0337V0.00617Nb0.0000604Co0.0460Al0.000624,1805.2\nFe0.814C0.000937Mn0.000717Si0.00200Cr0.0522Ni0.0977Mo0.0188V0.000110Nb0.0000605Co0.0000954Al0.0108Ti0.00282,1304.3\nFe0.814C0.0169Mn0.00236Si0.000201Cr0.0710Ni0.0000960Mo0.0338V0.00951Nb0.00249Co0.0488Al0.000627,1653.6\nFe0.816C0.000937Mn0.000102Si0.000200Cr0.000108Ni0.147Mo0.00821V0.000110Nb0.0000606Co0.0000955Al0.00250Ti0.0247,1792.2\nFe0.818C0.0178Mn0.00194Si0.000200Cr0.0799Ni0.0000958Mo0.0337V0.000662Nb0.0000605Co0.0466Al0.000625,1564.0\nFe0.819C0.00507Mn0.00686Si0.00493Cr0.127Ni0.0225Mo0.0102V0.00359N0.000791Nb0.0000596Co0.0000940Al0.000616,1021.0\nFe0.819C0.0150Mn0.00236Si0.000201Cr0.0716Ni0.0000960Mo0.0338V0.0102Nb0.0000606Co0.0468Al0.000626,1681.2\nFe0.822C0.000470Mn0.000616Si0.00161Cr0.0512Ni0.0971Mo0.0184V0.000111Nb0.0000607Co0.0000957Al0.00523Ti0.00271,1172.0\nFe0.823C0.0176Mn0.00183Si0.000198Cr0.0779Ni0.0000949Mo0.0219V0.0105Nb0.0000600Co0.0463Al0.000620,1722.5\nFe0.823Mn0.000618Si0.00101Cr0.0561Ni0.0984Mo0.0189V0.000111Nb0.0000609Co0.0000961Al0.000629Ti0.00106,1019.0\nFe0.825C0.0174Mn0.00175Si0.000201Cr0.0565Ni0.0000963Mo0.0344V0.0116Nb0.00554Co0.0468Al0.000628,1860.3\nFe0.858C0.0191Mn0.00194Si0.000199Cr0.0753Ni0.0000954Mo0.0341V0.0101Nb0.0000603Co0.000190Al0.000623,1812.1\nFe0.860C0.0125Mn0.00274Si0.000198Cr0.00439Ni0.0786Mo0.00284V0.000765Nb0.0000600Co0.0369Al0.000619,1139.7\n"
  },
  {
    "path": "dataset/matbench_steels/matbench_steels.json",
    "content": "[\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.794C0.000470Mn0.000617Si0.00101Cr0.0847Ni0.0981Mo0.0188V0.000111Nb0.0000608Co0.0000958Al0.00126Ti0.00118\\n\",\n        \"output\": \" 1036.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.659C0.00747Mn0.000102Si0.0134Cr0.156Ni0.0000955Mo0.0297V0.00451N0.000800Nb0.0000603Co0.128Al0.000831\\n\",\n        \"output\": \" 1412.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.646C0.00479Mn0.00597Si0.00492Cr0.135Ni0.0000980Mo0.0534V0.000113N0.000821Nb0.0000619Co0.148Al0.000640\\n\",\n        \"output\": \" 1228.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.703C0.00274Mn0.0209Si0.00625Cr0.173Ni0.0481Mo0.00864V0.000108Nb0.0000591Co0.0189Al0.0179\\n\",\n        \"output\": \" 1237.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.681C0.00744Mn0.000102Si0.000199Cr0.154Ni0.0000952Mo0.0175V0.0106N0.00120Nb0.0000601Co0.126Al0.00104\\n\",\n        \"output\": \" 1240.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.685C0.0112Mn0.000102Si0.000199Cr0.0957Ni0.0705Mo0.00991V0.00307Nb0.0000602Co0.123Al0.000622Ti0.000351\\n\",\n        \"output\": \" 1550.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.636C0.00881Mn0.000203Si0.00972Cr0.135Ni0.00892Mo0.0114V0.000109Nb0.0000600Co0.190Al0.000620\\n\",\n        \"output\": \" 1328.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.702C0.000943Mn0.000103Si0.000202Cr0.000109Ni0.142Mo0.000118V0.000111Nb0.0000609Co0.149Al0.000629Ti0.00509\\n\",\n        \"output\": \" 1144.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.822C0.000470Mn0.000616Si0.00161Cr0.0512Ni0.0971Mo0.0184V0.000111Nb0.0000607Co0.0000957Al0.00523Ti0.00271\\n\",\n        \"output\": \" 1172.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.770Mn0.000509Si0.000398Cr0.111Ni0.0972Mo0.0120V0.000110Nb0.0000602Co0.0000949Al0.00726Ti0.00199\\n\",\n        \"output\": \" 1243.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.712C0.00143Mn0.000104Si0.000203Cr0.000110Ni0.146Mo0.0297V0.000112Nb0.00123Co0.0852Al0.0207Ti0.00310\\n\",\n        \"output\": \" 1026.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.723C0.00320Mn0.00600Si0.00587Cr0.158Ni0.0655Mo0.0129V0.000108Nb0.0000591Co0.0000932Al0.0244\\n\",\n        \"output\": \" 1463.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.700C0.00927Mn0.000101Si0.00594Cr0.133Ni0.00901Mo0.0114V0.000109Nb0.000479Co0.130Al0.000619\\n\",\n        \"output\": \" 1299.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.753C0.00929Mn0.000102Si0.000199Cr0.0880Ni0.0200Mo0.00756V0.00318Nb0.0000600Co0.117Al0.000620Ti0.000233\\n\",\n        \"output\": \" 1357.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength. ->\",\n        \"input\": \" Fe0.721C0.00970Mn0.000101Si0.0119Cr0.0875Ni0.0246Mo0.00752V0.00316Nb0.0000597Co0.134Al0.000617Ti0.000232.\\n\",\n        \"output\": \" Unable to answer due to lack of conditions.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.721C0.00191Mn0.000104Si0.000204Cr0.000110Ni0.147Mo0.0299V0.000113Nb0.00123Co0.0856Al0.0106Ti0.00288\\n\",\n        \"output\": \" 1019.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.711C0.00931Mn0.000102Si0.000199Cr0.113Ni0.0237Mo0.0115V0.000110Nb0.000602Co0.130Al0.000622\\n\",\n        \"output\": \" 1282.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.758C0.00142Mn0.000104Si0.000203Cr0.123Ni0.0932Mo0.000119V0.000112Nb0.0000612Co0.0000965W0.0124Al0.00822Ti0.00309\\n\",\n        \"output\": \" 1199.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.661C0.000475Mn0.000520Si0.00102Cr0.000110Ni0.170Mo0.0247V0.000112Nb0.0000615Co0.111Al0.0131Ti0.0177\\n\",\n        \"output\": \" 2510.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.705C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.147Mo0.0304V0.000112Nb0.0000615Co0.0891Al0.0195Ti0.00835\\n\",\n        \"output\": \" 1580.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.768C0.000931Mn0.00244Si0.00199Cr0.110Ni0.0981Mo0.0113V0.000110Nb0.0000602Co0.0000948Al0.00497Ti0.00269\\n\",\n        \"output\": \" 1167.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.823Mn0.000618Si0.00101Cr0.0561Ni0.0984Mo0.0189V0.000111Nb0.0000609Co0.0000961Al0.000629Ti0.00106\\n\",\n        \"output\": \" 1019.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.799C0.000468Mn0.0256Si0.000401Cr0.000108Ni0.173Mo0.000117V0.000110Nb0.0000605Co0.0000955Al0.00104Ti0.000470\\n\",\n        \"output\": \" 1471.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.779C0.00141Mn0.000103Si0.000201Cr0.000109Ni0.174Mo0.0130V0.000111Nb0.0000608Co0.0000959Al0.00209Ti0.0295\\n\",\n        \"output\": \" 2006.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.804C0.0166Mn0.00238Si0.000202Cr0.0782Ni0.0000969Mo0.0343V0.0114Nb0.0000612Co0.0473W0.00476Al0.000632\\n\",\n        \"output\": \" 1688.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.674C0.0112Mn0.000102Si0.000199Cr0.0957Ni0.0829Mo0.00874V0.00307Nb0.0000602Co0.123Al0.000622Ti0.000234\\n\",\n        \"output\": \" 1309.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.802C0.000468Mn0.000512Si0.00120Cr0.0526Ni0.111Mo0.0173V0.000110Nb0.0000605Co0.0000954Al0.0121Ti0.00258\\n\",\n        \"output\": \" 1437.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.786C0.000469Mn0.000512Si0.00120Cr0.0576Ni0.124Mo0.0172V0.000110Nb0.0000606Co0.0000955Al0.0106Ti0.00235\\n\",\n        \"output\": \" 1404.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.799C0.000471Mn0.000103Si0.000201Cr0.000109Ni0.165Mo0.0118V0.000111Nb0.0000609Co0.0000960Al0.00147Ti0.0215\\n\",\n        \"output\": \" 1874.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.672C0.00473Mn0.00527Si0.00647Cr0.131Ni0.0000968Mo0.0373V0.000111N0.00162Nb0.0000611Co0.141Al0.000631\\n\",\n        \"output\": \" 1155.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.673C0.000908Mn0.0000992Si0.0361Cr0.167Ni0.0372Mo0.000114V0.000107Nb0.0000587Co0.0851Al0.000404Ti0.000569\\n\",\n        \"output\": \" 1143.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.674C0.00752Mn0.000103Si0.000201Cr0.156Ni0.0000961Mo0.0303V0.000111N0.00121Nb0.0000607Co0.129Al0.00146\\n\",\n        \"output\": \" 1460.7\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.751C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0128V0.000109Nb0.0000596Co0.0000939Al0.0220Ti0.000578\\n\",\n        \"output\": \" 1317.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.747C0.000899Mn0.000982Si0.0820Cr0.000104Ni0.166Mo0.000112V0.000106Nb0.0000581Co0.0000916Al0.00140Ti0.00101\\n\",\n        \"output\": \" 1801.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.689C0.000476Mn0.000104Si0.000204Cr0.111Ni0.0683Mo0.0327V0.000112Nb0.0000615Co0.0975Al0.000636\\n\",\n        \"output\": \" 1486.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.764C0.000467Mn0.000511Si0.00200Cr0.0831Ni0.117Mo0.0178V0.000110Nb0.0000604Co0.0000952Al0.0131Ti0.00234\\n\",\n        \"output\": \" 1506.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.682C0.00925Mn0.000101Si0.0101Cr0.134Ni0.00899Mo0.0115V0.000109Nb0.000479Co0.143Al0.000618\\n\",\n        \"output\": \" 1314.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.795C0.00141Mn0.000717Si0.000801Cr0.0963Ni0.0810Mo0.0191V0.000110Nb0.0000606Co0.0000955Al0.00313Ti0.00270\\n\",\n        \"output\": \" 1150.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.683C0.00749Mn0.000102Si0.000200Cr0.156Ni0.0000958Mo0.0309V0.00453N0.00522Nb0.0000605Co0.112Al0.000834\\n\",\n        \"output\": \" 1646.7\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.782C0.0181Mn0.00187Si0.000203Cr0.0816Ni0.0000973Mo0.0576V0.0108Nb0.0000615Co0.0476Al0.000635\\n\",\n        \"output\": \" 1577.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.680Mn0.000102Si0.000199Cr0.127Ni0.0976Mo0.00856V0.000110Nb0.0000601Co0.0709Al0.00891Ti0.00654\\n\",\n        \"output\": \" 1586.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.661C0.000454Mn0.0000993Si0.0375Cr0.164Ni0.0381Mo0.000114V0.000107Nb0.0000587Co0.0972Al0.000606Ti0.000684\\n\",\n        \"output\": \" 1185.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.684C0.00699Mn0.000102Si0.000199Cr0.155Ni0.0000953Mo0.0177V0.00450N0.00120Nb0.0000602Co0.130Al0.000622\\n\",\n        \"output\": \" 1233.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.688C0.00877Mn0.000101Si0.00987Cr0.134Ni0.00898Mo0.00856V0.000109Nb0.0000597Co0.141Al0.000617\\n\",\n        \"output\": \" 1311.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.766C0.00140Mn0.000102Si0.000199Cr0.115Ni0.0900Mo0.0143V0.000110Nb0.0000601Co0.0000948Al0.00952Ti0.00327\\n\",\n        \"output\": \" 1182.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.694C0.0103Mn0.000102Si0.000200Cr0.0917Ni0.0440Mo0.00877V0.00308Nb0.0000604Co0.146W0.00153Al0.000624Ti0.000352\\n\",\n        \"output\": \" 1575.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.620C0.000953Mn0.000521Si0.00102Cr0.000110Ni0.192Mo0.0176V0.000112Nb0.0000616Co0.146Al0.00318Ti0.0185\\n\",\n        \"output\": \" 2411.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.803C0.0174Mn0.00236Si0.000201Cr0.0779Ni0.0000960Mo0.0335V0.0122Nb0.00473Co0.0477Al0.000627\\n\",\n        \"output\": \" 1340.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \"wallet\",\n        \"output\": \" wallet is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength. ->\",\n        \"input\": \" Fe0.682C0.00877Mn0.000202Si0.00967Cr0.134Ni0.00907Mo0.00861V0.00501Nb0.0000597Co0.142Al0.000616.\\n\",\n        \"output\": \" Unable to answer due to lack of conditions.\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.683C0.00704Mn0.000103Si0.000201Cr0.156Ni0.0000961Mo0.0299V0.00454N0.00121Nb0.0000607Co0.117Al0.000836\\n\",\n        \"output\": \" 1471.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.745C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0794Mo0.0129V0.000108Nb0.0000594Co0.0000937Al0.0268Ti0.000115\\n\",\n        \"output\": \" 1521.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.758C0.00185Mn0.000101Si0.000198Cr0.132Ni0.0780Mo0.0127V0.000109Nb0.0000597Co0.0000942Al0.0167Ti0.000348\\n\",\n        \"output\": \" 1305.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.779C0.00139Mn0.000101Si0.000198Cr0.114Ni0.0973Mo0.000116V0.000109Nb0.0000597Co0.0000941Al0.00432Ti0.00359\\n\",\n        \"output\": \" 1125.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.703C0.00927Mn0.000101Si0.000198Cr0.128Ni0.0235Mo0.00574V0.000109Nb0.000599Co0.129Al0.000619\\n\",\n        \"output\": \" 1273.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition. ->\",\n        \"input\": \" Fe0.671C0.000470Mn0.000514Si0.00100Cr0.000109Ni0.141Mo0.00882V0.000111Nb0.0000607Co0.147Al0.0159Ti0.0137.\\n\",\n        \"output\": \" Unable to answer due to lack of conditions.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.744C0.00414Mn0.0217Si0.00354Cr0.180Ni0.0401Mo0.00598V0.000108Nb0.0000594Co0.0000937Al0.000614\\n\",\n        \"output\": \" 1028.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.780C0.000465Mn0.00122Si0.00159Cr0.105Ni0.0953Mo0.00991V0.000110Nb0.0000602Co0.0000949Al0.00414Ti0.00222\\n\",\n        \"output\": \" 1087.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.773C0.000933Mn0.000612Si0.00259Cr0.112Ni0.0945Mo0.0126V0.000110Nb0.0000603Co0.0000950Al0.00187Ti0.00152\\n\",\n        \"output\": \" 1005.9\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.684C0.00920Mn0.000101Si0.0197Cr0.134Ni0.00885Mo0.0114V0.00228Nb0.000476Co0.129Al0.000614\\n\",\n        \"output\": \" 1344.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.703C0.00883Mn0.000102Si0.000199Cr0.135Ni0.00942Mo0.0115V0.000110Nb0.000421Co0.131Al0.000621\\n\",\n        \"output\": \" 1371.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.785C0.000931Mn0.000102Si0.000199Cr0.000108Ni0.167Mo0.000117V0.0209Nb0.0000602Co0.0000949Al0.00187Ti0.0241\\n\",\n        \"output\": \" 1730.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.686C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.143Mo0.0185V0.000113Nb0.0000618Co0.150Al0.000638Ti0.00144\\n\",\n        \"output\": \" 1267.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.730C0.00414Mn0.0101Si0.00983Cr0.186Ni0.0395Mo0.0158V0.000108N0.00394Nb0.0000594Co0.0000937Al0.000614\\n\",\n        \"output\": \" 1016.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.713C0.0108Mn0.000102Si0.000200Cr0.0336Ni0.107Mo0.00691V0.000110Nb0.0000605Co0.128Al0.000208Ti0.000117\\n\",\n        \"output\": \" 1746.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.707C0.000959Mn0.000105Si0.000205Cr0.000111Ni0.182Mo0.0306V0.000113Nb0.0000620Co0.0655Al0.00256Ti0.0107\\n\",\n        \"output\": \" 1088.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.752C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0781Mo0.0127V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0215Ti0.000578\\n\",\n        \"output\": \" 1276.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.713C0.0108Mn0.000102Si0.000200Cr0.0335Ni0.106Mo0.00697V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000117\\n\",\n        \"output\": \" 1741.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.656C0.00758Mn0.000104Si0.000203Cr0.156Ni0.0000970Mo0.0424V0.00458N0.00122Nb0.0000613Co0.131Al0.000844\\n\",\n        \"output\": \" 1460.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.692C0.00837Mn0.00112Si0.00179Cr0.000107Ni0.169Mo0.000116V0.0474Nb0.0000601Co0.0764Al0.00228Ti0.000933\\n\",\n        \"output\": \" 1605.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.678C0.00421Mn0.00645Si0.00741Cr0.133Ni0.0000958Mo0.0233V0.000110N0.00161Nb0.0000605Co0.145Al0.000625\\n\",\n        \"output\": \" 1131.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.787C0.0137Mn0.000103Si0.000202Cr0.0111Ni0.101Mo0.0118V0.00111Nb0.0000610Co0.0689W0.00394Al0.000630Ti0.000118\\n\",\n        \"output\": \" 1683.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.715C0.00378Mn0.00609Si0.00605Cr0.133Ni0.0000966Mo0.0372V0.000111N0.00202Nb0.0000610Co0.0962Al0.000630\\n\",\n        \"output\": \" 1287.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.740C0.00457Mn0.0300Si0.00586Cr0.179Ni0.0393Mo0.000114V0.000108Nb0.0000591Co0.0000931Al0.000610\\n\",\n        \"output\": \" 1130.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.692C0.00968Mn0.000101Si0.0144Cr0.133Ni0.00887Mo0.0114V0.000109Nb0.000477Co0.130Al0.000616\\n\",\n        \"output\": \" 1369.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.693C0.00877Mn0.000101Si0.0144Cr0.133Ni0.00897Mo0.0114V0.000109Nb0.000477Co0.130Al0.000616\\n\",\n        \"output\": \" 1275.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.762C0.000930Mn0.00752Si0.00199Cr0.110Ni0.0971Mo0.0115V0.000110Nb0.0000601Co0.0000948Al0.00621Ti0.00257\\n\",\n        \"output\": \" 1145.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.669C0.00331Mn0.00590Si0.00648Cr0.129Ni0.0000969Mo0.0375V0.000112N0.00203Nb0.0000612Co0.147Al0.000632\\n\",\n        \"output\": \" 1133.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.783C0.0187Mn0.00184Si0.000200Cr0.104Ni0.0000955Mo0.0341V0.0106Nb0.0000603Co0.0463Al0.000623\\n\",\n        \"output\": \" 1798.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.773C0.00141Mn0.000512Si0.00220Cr0.0812Ni0.116Mo0.0179V0.000110Nb0.0000606Co0.0000955Al0.00522Ti0.00235\\n\",\n        \"output\": \" 1218.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.668Mn0.000102Si0.000200Cr0.119Ni0.0767Mo0.0292V0.000111Nb0.0000606Co0.0813Al0.0248Ti0.000235\\n\",\n        \"output\": \" 1837.9\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.800C0.000470Mn0.000616Si0.000602Cr0.0506Ni0.117Mo0.0186V0.000111Nb0.0000607Co0.0000957Al0.00982Ti0.00224\\n\",\n        \"output\": \" 1390.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.710C0.000477Mn0.000104Si0.000204Cr0.000110Ni0.149Mo0.0305V0.000112Nb0.0000617Co0.0885Al0.0127Ti0.00814\\n\",\n        \"output\": \" 1123.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.784C0.000919Mn0.00100Si0.0397Cr0.000106Ni0.173Mo0.000115V0.000108Nb0.0000594Co0.0000936Al0.000614\\n\",\n        \"output\": \" 1298.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.811C0.0182Mn0.00225Si0.000200Cr0.0755Ni0.0000957Mo0.0337V0.0119Nb0.0000605Co0.0467Al0.000625\\n\",\n        \"output\": \" 1688.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.801C0.000939Mn0.000821Si0.000803Cr0.0513Ni0.116Mo0.0185V0.000111Nb0.0000607Co0.0000957Al0.00794Ti0.00271\\n\",\n        \"output\": \" 1243.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.801C0.000934Mn0.000102Si0.000200Cr0.000108Ni0.171Mo0.00175V0.000110Nb0.0000604Co0.0000952Al0.00208Ti0.0229\\n\",\n        \"output\": \" 1674.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.665C0.000468Mn0.000102Si0.000200Cr0.121Ni0.0768Mo0.0293V0.000110Nb0.0000606Co0.0823Al0.0254Ti0.000118\\n\",\n        \"output\": \" 1870.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.751C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0786Mo0.0127V0.000109Nb0.0000596Co0.0000939Al0.0213Ti0.00116\\n\",\n        \"output\": \" 1348.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.768C0.000466Mn0.000306Si0.000598Cr0.110Ni0.100Mo0.0128V0.000110Nb0.0000603Co0.0000951Al0.00478Ti0.00281\\n\",\n        \"output\": \" 1340.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.682C0.00877Mn0.000202Si0.00967Cr0.134Ni0.00907Mo0.00861V0.00501Nb0.0000597Co0.142Al0.000616\\n\",\n        \"output\": \" 1241.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.801C0.000469Mn0.00103Si0.00361Cr0.0528Ni0.116Mo0.0175V0.000111Nb0.0000607Co0.0000957Al0.00522Ti0.00177\\n\",\n        \"output\": \" 1230.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.667C0.00984Mn0.000102Si0.000200Cr0.158Ni0.0000959Mo0.0295V0.00453N0.000804Nb0.0000606Co0.129Al0.00104\\n\",\n        \"output\": \" 1405.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.752C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0783Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0209Ti0.00104\\n\",\n        \"output\": \" 1391.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.735C0.00514Mn0.00593Si0.00440Cr0.128Ni0.0000957Mo0.0227V0.000110N0.000802Nb0.0000604Co0.0972Al0.000624\\n\",\n        \"output\": \" 1096.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.751C0.00563Mn0.00185Si0.00120Cr0.0218Ni0.0967Mo0.00587V0.000111Nb0.0000606Co0.116Al0.000209\\n\",\n        \"output\": \" 1463.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.819C0.0150Mn0.00236Si0.000201Cr0.0716Ni0.0000960Mo0.0338V0.0102Nb0.0000606Co0.0468Al0.000626\\n\",\n        \"output\": \" 1681.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.670C0.00564Mn0.000103Si0.000201Cr0.158Ni0.0000963Mo0.0300V0.00477N0.00121Nb0.0000608Co0.129Al0.000628\\n\",\n        \"output\": \" 1515.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.702Mn0.000102Si0.000200Cr0.154Ni0.0793Mo0.0152V0.000110Nb0.0000604Co0.0409Al0.00208Ti0.00574\\n\",\n        \"output\": \" 1350.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.711C0.00699Mn0.000102Si0.000199Cr0.0969Ni0.0458Mo0.00875V0.00549Nb0.0000603Co0.123Al0.000622Ti0.000234\\n\",\n        \"output\": \" 1412.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.750C0.00184Mn0.000101Si0.000394Cr0.133Ni0.0814Mo0.0121V0.000109Nb0.0000596Co0.0000939Al0.0205\\n\",\n        \"output\": \" 1308.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.706C0.0116Mn0.000101Si0.000199Cr0.0965Ni0.0589Mo0.00755V0.00317Nb0.0000600Co0.115Al0.000620Ti0.000349\\n\",\n        \"output\": \" 1405.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.719C0.000945Mn0.000103Si0.000202Cr0.0557Ni0.108Mo0.0302V0.000111Nb0.0000611Co0.0597Al0.0149Ti0.0111\\n\",\n        \"output\": \" 1071.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.671C0.00376Mn0.000103Si0.000201Cr0.157Ni0.0000962Mo0.0294V0.00510N0.00282Nb0.0000608Co0.130Al0.000628\\n\",\n        \"output\": \" 1311.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.752C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0787Mo0.0129V0.000109Nb0.0000596Co0.0000940Al0.0213Ti0.000116\\n\",\n        \"output\": \" 1312.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.672C0.00564Mn0.000103Si0.000201Cr0.156Ni0.0000962Mo0.0294V0.00454N0.00121Nb0.0000608Co0.129Al0.00105\\n\",\n        \"output\": \" 1322.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.678C0.000464Mn0.000102Si0.000199Cr0.0873Ni0.114Mo0.000116V0.000110Nb0.0000600Co0.0992Al0.00806Ti0.0129\\n\",\n        \"output\": \" 1768.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.707C0.000959Mn0.000105Si0.000205Cr0.000111Ni0.183Mo0.0306V0.000113Nb0.0000620Co0.0675Al0.00256Ti0.00770\\n\",\n        \"output\": \" 1026.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.753C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0127V0.000109Nb0.0000596Co0.0000940Al0.0211Ti0.000231\\n\",\n        \"output\": \" 1276.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.787C0.000474Mn0.000207Si0.000203Cr0.000109Ni0.176Mo0.0181V0.000112Nb0.0000612Co0.0000965Al0.00190Ti0.0150\\n\",\n        \"output\": \" 1599.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.674C0.00925Mn0.00516Si0.0101Cr0.135Ni0.00975Mo0.0115V0.000109Nb0.0000598Co0.145Al0.000618\\n\",\n        \"output\": \" 1300.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.725C0.0155Mn0.000677Si0.0899Cr0.000102Ni0.167Mo0.000111V0.000104Nb0.0000572Co0.0000902Al0.000591\\n\",\n        \"output\": \" 1250.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.657C0.000954Mn0.000522Si0.00102Cr0.000110Ni0.166Mo0.0243V0.00776Nb0.0000617Co0.120Al0.00340Ti0.0189\\n\",\n        \"output\": \" 2381.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.797C0.000939Mn0.00215Si0.00381Cr0.0540Ni0.118Mo0.0175V0.000111Nb0.0000607Co0.0000957Al0.00481Ti0.00165\\n\",\n        \"output\": \" 1194.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.750C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0789Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0218Ti0.00104\\n\",\n        \"output\": \" 1350.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.707C0.0112Mn0.000102Si0.000199Cr0.0956Ni0.0485Mo0.00990V0.00318Nb0.0000601Co0.123Al0.000621Ti0.000350\\n\",\n        \"output\": \" 1429.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.712C0.00144Mn0.000105Si0.000205Cr0.000111Ni0.180Mo0.0306V0.000113Nb0.0000620Co0.0655Al0.00235Ti0.00842\\n\",\n        \"output\": \" 1109.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.675C0.00705Mn0.000103Si0.000201Cr0.157Ni0.0000962Mo0.0294V0.000111Nb0.0000608Co0.129Al0.00105\\n\",\n        \"output\": \" 1338.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.699C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.166Mo0.0287V0.00383Nb0.0000618Co0.0847Al0.00829Ti0.00803\\n\",\n        \"output\": \" 1287.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.650C0.000477Mn0.000522Si0.00102Cr0.000110Ni0.176Mo0.0215V0.000113Nb0.0000617Co0.126Al0.00170Ti0.0225\\n\",\n        \"output\": \" 2411.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.741C0.00702Mn0.00164Si0.00100Cr0.0321Ni0.0964Mo0.00586V0.000110Nb0.0000605Co0.115Al0.000208\\n\",\n        \"output\": \" 1455.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.858C0.0191Mn0.00194Si0.000199Cr0.0753Ni0.0000954Mo0.0341V0.0101Nb0.0000603Co0.000190Al0.000623\\n\",\n        \"output\": \" 1812.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.777C0.000470Mn0.000719Si0.00201Cr0.0836Ni0.115Mo0.0178V0.000111Nb0.0000607Co0.0000958Al0.00167Ti0.000707\\n\",\n        \"output\": \" 1010.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.766C0.000468Mn0.000819Si0.00100Cr0.102Ni0.103Mo0.0188V0.000110Nb0.0000606Co0.0000955Al0.00563Ti0.00259\\n\",\n        \"output\": \" 1267.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.714C0.00984Mn0.000102Si0.000200Cr0.0336Ni0.106Mo0.00698V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000118\\n\",\n        \"output\": \" 1795.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.687C0.0162Mn0.000101Si0.000199Cr0.0965Ni0.0142Mo0.0116V0.00328Nb0.0000600Co0.170Al0.000620Ti0.000233\\n\",\n        \"output\": \" 1731.7\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.793C0.000468Mn0.000819Si0.00240Cr0.0962Ni0.0800Mo0.0190V0.000110Nb0.0000605Co0.0000954Al0.00521Ti0.00235\\n\",\n        \"output\": \" 1169.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.727C0.000476Mn0.000104Si0.000203Cr0.0549Ni0.108Mo0.0304V0.000112Nb0.0000615Co0.0611Al0.00212Ti0.0154\\n\",\n        \"output\": \" 1123.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.751C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0787Mo0.0128V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0217Ti0.000231\\n\",\n        \"output\": \" 1269.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.687C0.00974Mn0.000101Si0.000198Cr0.151Ni0.00883Mo0.0116V0.000109Nb0.000480Co0.131Al0.000620\\n\",\n        \"output\": \" 1372.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.801C0.000470Mn0.000205Si0.000603Cr0.0543Ni0.117Mo0.0176V0.000111Nb0.0000607Co0.0000958Al0.00648Ti0.00248\\n\",\n        \"output\": \" 1309.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.781C0.00141Mn0.000103Si0.000201Cr0.000109Ni0.167Mo0.000118V0.0200Nb0.0152Co0.0000960Al0.00210Ti0.0126\\n\",\n        \"output\": \" 1730.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.816C0.000937Mn0.000102Si0.000200Cr0.000108Ni0.147Mo0.00821V0.000110Nb0.0000606Co0.0000955Al0.00250Ti0.0247\\n\",\n        \"output\": \" 1792.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.796C0.000469Mn0.000103Si0.000201Cr0.000108Ni0.174Mo0.00587V0.000111Nb0.0000606Co0.0000956Al0.00167Ti0.0212\\n\",\n        \"output\": \" 1737.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.780C0.000457Mn0.000599Si0.0504Cr0.000106Ni0.166Mo0.000114V0.000108Nb0.0000591Co0.0000931Al0.00102Ti0.000802\\n\",\n        \"output\": \" 1309.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.737C0.0111Mn0.000101Si0.000198Cr0.0964Ni0.0266Mo0.00755V0.00317Nb0.0000599Co0.117Al0.000619Ti0.000233\\n\",\n        \"output\": \" 1564.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.752C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0784Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0209Ti0.000116\\n\",\n        \"output\": \" 1277.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.814C0.000937Mn0.000717Si0.00200Cr0.0522Ni0.0977Mo0.0188V0.000110Nb0.0000605Co0.0000954Al0.0108Ti0.00282\\n\",\n        \"output\": \" 1304.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.673C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.180Mo0.0286V0.00482Nb0.0000614Co0.0842Al0.0201Ti0.00858\\n\",\n        \"output\": \" 1288.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.699C0.000946Mn0.000103Si0.000202Cr0.000109Ni0.140Mo0.00545V0.000112Nb0.0000612Co0.148Al0.000632Ti0.00487\\n\",\n        \"output\": \" 1212.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.755C0.00552Mn0.00543Si0.0236Cr0.128Ni0.0188Mo0.0173V0.00380N0.00197Nb0.00244Co0.0375Al0.000615\\n\",\n        \"output\": \" 1074.9\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.770C0.000470Mn0.000103Si0.000201Cr0.000109Ni0.168Mo0.0124V0.0222Nb0.0000607Co0.0000957Al0.00251Ti0.0236\\n\",\n        \"output\": \" 1998.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.802C0.0174Mn0.00185Si0.000201Cr0.0805Ni0.0000962Mo0.0403V0.0106Nb0.0000608Co0.0468Al0.000628\\n\",\n        \"output\": \" 1784.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.690C0.00697Mn0.000102Si0.000199Cr0.150Ni0.00885Mo0.0116V0.000110Nb0.000481Co0.130Al0.000621\\n\",\n        \"output\": \" 1278.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.664C0.00751Mn0.00575Si0.000201Cr0.157Ni0.0000961Mo0.0301V0.00454N0.00121Nb0.0000607Co0.128Al0.00105\\n\",\n        \"output\": \" 1350.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.724C0.00140Mn0.000510Si0.00339Cr0.000108Ni0.157Mo0.000117V0.0440Nb0.0000603Co0.0656Al0.00208Ti0.00164\\n\",\n        \"output\": \" 1536.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.759C0.000472Mn0.000103Si0.000202Cr0.000109Ni0.203Mo0.0124V0.000111Nb0.0000610Co0.0000961Al0.00273Ti0.0225\\n\",\n        \"output\": \" 1661.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.779C0.00141Mn0.000103Si0.000201Cr0.000109Ni0.174Mo0.0130V0.000111Nb0.0000608Co0.0000959Al0.00230Ti0.0295\\n\",\n        \"output\": \" 2005.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.721C0.00189Mn0.00455Si0.00647Cr0.131Ni0.0000967Mo0.0364V0.000111N0.00122Nb0.0000611Co0.0963Al0.000631\\n\",\n        \"output\": \" 1219.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.766Mn0.00366Si0.00159Cr0.110Ni0.0981Mo0.0118V0.000110Nb0.0000602Co0.0000949Al0.00622Ti0.00269\\n\",\n        \"output\": \" 1178.9\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.803Mn0.000512Si0.00120Cr0.0520Ni0.110Mo0.0173V0.000110Nb0.0000605Co0.0000954Al0.0137Ti0.00235\\n\",\n        \"output\": \" 1451.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.669C0.00957Mn0.0000996Si0.0388Cr0.132Ni0.00876Mo0.0113V0.000107Nb0.000471Co0.129Al0.000608\\n\",\n        \"output\": \" 1354.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \"samurai\",\n        \"output\": \" samurai is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.721C0.000955Mn0.000104Si0.000204Cr0.000110Ni0.143Mo0.0299V0.00484Nb0.00124Co0.0867Al0.0102Ti0.00240\\n\",\n        \"output\": \" 1026.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.663C0.00329Mn0.000103Si0.000201Cr0.169Ni0.0000963Mo0.0294V0.00455N0.00121Nb0.0000608Co0.129Al0.000629\\n\",\n        \"output\": \" 1312.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.763Mn0.00102Si0.00814Cr0.109Ni0.0988Mo0.0116V0.000109Nb0.0000600Co0.0000946Al0.00517Ti0.00268\\n\",\n        \"output\": \" 1221.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.706C0.000906Mn0.0000990Si0.0372Cr0.162Ni0.0361Mo0.000113V0.000107Nb0.0000586Co0.0554Al0.000806Ti0.000796\\n\",\n        \"output\": \" 1109.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.780C0.000467Mn0.000510Si0.00200Cr0.0830Ni0.0993Mo0.0179V0.000110Nb0.0000603Co0.0000951Al0.0139Ti0.00234\\n\",\n        \"output\": \" 1475.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.668C0.000469Mn0.000102Si0.000200Cr0.119Ni0.0764Mo0.0293V0.000110Nb0.0000606Co0.0817Al0.0252Ti0.000118\\n\",\n        \"output\": \" 1825.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.757C0.00185Mn0.000101Si0.000791Cr0.133Ni0.0781Mo0.0127V0.000109Nb0.0000597Co0.0000942Al0.0158Ti0.000232\\n\",\n        \"output\": \" 1280.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.819C0.00507Mn0.00686Si0.00493Cr0.127Ni0.0225Mo0.0102V0.00359N0.000791Nb0.0000596Co0.0000940Al0.000616\\n\",\n        \"output\": \" 1021.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.702C0.00930Mn0.000102Si0.000199Cr0.133Ni0.0115Mo0.0117V0.000110Nb0.000481Co0.131Al0.000621\\n\",\n        \"output\": \" 1423.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.687C0.000467Mn0.000102Si0.000200Cr0.0835Ni0.114Mo0.00573V0.000110Nb0.0000604Co0.0947Al0.00562Ti0.00832\\n\",\n        \"output\": \" 1779.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.721C0.00970Mn0.000101Si0.0119Cr0.0875Ni0.0246Mo0.00752V0.00316Nb0.0000597Co0.134Al0.000617Ti0.000232\\n\",\n        \"output\": \" 1391.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.752C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0218Ti0.000231\\n\",\n        \"output\": \" 1296.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.634C0.000478Mn0.000523Si0.00102Cr0.000111Ni0.173Mo0.0237V0.000113Nb0.0000619Co0.146Al0.00277Ti0.0176\\n\",\n        \"output\": \" 2487.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.732C0.00415Mn0.00504Si0.00553Cr0.182Ni0.0395Mo0.0117V0.000109Nb0.0000597Co0.0190Al0.000616\\n\",\n        \"output\": \" 1117.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.778Mn0.00122Si0.00159Cr0.112Ni0.0876Mo0.0115V0.000110Nb0.0000602Co0.0000949Al0.00539Ti0.00245\\n\",\n        \"output\": \" 1207.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.689C0.00193Mn0.000105Si0.000206Cr0.000111Ni0.185Mo0.0362V0.000114Nb0.0000623Co0.0785Al0.00343Ti0.00507\\n\",\n        \"output\": \" 1012.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.693C0.000454Mn0.0000993Si0.0334Cr0.165Ni0.0381Mo0.000114V0.000107Nb0.0000587Co0.0685Al0.000405Ti0.000456\\n\",\n        \"output\": \" 1205.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.754C0.00184Mn0.000101Si0.000197Cr0.132Ni0.0780Mo0.0128V0.000109Nb0.0000596Co0.0000940Al0.0213Ti0.000347\\n\",\n        \"output\": \" 1294.9\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.760C0.000468Mn0.000102Si0.000200Cr0.113Ni0.0986Mo0.0181V0.000110Nb0.0000605Co0.0000953Al0.00749Ti0.00129\\n\",\n        \"output\": \" 1091.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.767C0.000465Mn0.00112Si0.00358Cr0.110Ni0.0981Mo0.0119V0.000110Nb0.0000601Co0.0000948Al0.00559Ti0.00257\\n\",\n        \"output\": \" 1175.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.656C0.00930Mn0.000102Si0.000199Cr0.152Ni0.00875Mo0.0116V0.000110Nb0.000481Co0.161Al0.000621\\n\",\n        \"output\": \" 1243.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.771Mn0.00122Si0.00140Cr0.107Ni0.100Mo0.0123V0.000110Nb0.0000603Co0.0000950Al0.00477Ti0.00257\\n\",\n        \"output\": \" 1150.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.690C0.00970Mn0.000101Si0.0111Cr0.134Ni0.00936Mo0.0114V0.00370Nb0.000478Co0.129Al0.000617\\n\",\n        \"output\": \" 1280.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.813C0.0187Mn0.00143Si0.000200Cr0.0800Ni0.0000957Mo0.0337V0.00617Nb0.0000604Co0.0460Al0.000624\\n\",\n        \"output\": \" 1805.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.664C0.00754Mn0.000103Si0.000604Cr0.152Ni0.0105Mo0.0292V0.000111Nb0.00164Co0.134Al0.000629\\n\",\n        \"output\": \" 1169.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.768C0.000466Mn0.00122Si0.00119Cr0.111Ni0.0972Mo0.0119V0.000110Nb0.0000602Co0.0000949Al0.00642Ti0.00245\\n\",\n        \"output\": \" 1258.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.814C0.0169Mn0.00236Si0.000201Cr0.0710Ni0.0000960Mo0.0338V0.00951Nb0.00249Co0.0488Al0.000627\\n\",\n        \"output\": \" 1653.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.648C0.000453Mn0.0000991Si0.0386Cr0.183Ni0.0195Mo0.000113V0.000107Nb0.0000586Co0.109Al0.000605Ti0.000569\\n\",\n        \"output\": \" 1088.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.648C0.00751Mn0.000103Si0.000201Cr0.158Ni0.0000961Mo0.0288V0.00531N0.00201Nb0.0000607Co0.149Al0.000836\\n\",\n        \"output\": \" 1502.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.721C0.000955Mn0.000104Si0.000204Cr0.000110Ni0.146Mo0.0287V0.00293Nb0.0000617Co0.0846Al0.00765Ti0.00850\\n\",\n        \"output\": \" 1164.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.722C0.00797Mn0.00164Si0.00100Cr0.0322Ni0.0961Mo0.00710V0.000111Nb0.0000606Co0.131Al0.000209\\n\",\n        \"output\": \" 1547.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.652Mn0.000522Si0.00102Cr0.000110Ni0.177Mo0.0209V0.000113Nb0.0000617Co0.126Al0.00212Ti0.0194\\n\",\n        \"output\": \" 2331.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.802Mn0.000410Si0.00120Cr0.0543Ni0.114Mo0.0175V0.000111Nb0.0000607Co0.0000957Al0.00815Ti0.00236\\n\",\n        \"output\": \" 1324.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition. ->\",\n        \"input\": \" Fe0.802C0.000468Mn0.000512Si0.00120Cr0.0526Ni0.111Mo0.0173V0.000110Nb0.0000605Co0.0000954Al0.0121Ti0.00258.\\n\",\n        \"output\": \" Unable to answer due to lack of conditions.\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.713C0.0112Mn0.000102Si0.000200Cr0.0337Ni0.106Mo0.00697V0.000110Nb0.0000605Co0.128Al0.000208Ti0.000117\\n\",\n        \"output\": \" 1804.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.765Mn0.00112Si0.00597Cr0.110Ni0.0990Mo0.0119V0.000110Nb0.0000601Co0.0000948Al0.00414Ti0.00257\\n\",\n        \"output\": \" 1173.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.670C0.00439Mn0.00704Si0.00563Cr0.138Ni0.0000999Mo0.000122V0.000115N0.00126Nb0.0000631Co0.147W0.0255Al0.000652\\n\",\n        \"output\": \" 1081.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.667C0.000477Mn0.000522Si0.00102Cr0.000110Ni0.171Mo0.0233V0.000113Nb0.0000617Co0.115Al0.00361Ti0.0184\\n\",\n        \"output\": \" 2381.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.682C0.00515Mn0.000102Si0.000200Cr0.0995Ni0.0355Mo0.0117V0.00552Nb0.0000605Co0.159Al0.000625Ti0.000353\\n\",\n        \"output\": \" 1453.8\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.718C0.000473Mn0.000103Si0.000606Cr0.0866Ni0.0969Mo0.00118N0.000405Co0.0784W0.00707Al0.00421Ti0.00581\\n\",\n        \"output\": \" 1525.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.812C0.000934Mn0.000715Si0.00220Cr0.0507Ni0.0975Mo0.0181V0.000110Nb0.0000604Co0.0000952Al0.0146Ti0.00258\\n\",\n        \"output\": \" 1420.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.751C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0783Mo0.0129V0.000109Nb0.0000596Co0.0000939Al0.0220Ti0.000116\\n\",\n        \"output\": \" 1297.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.686C0.000466Mn0.000102Si0.000199Cr0.0951Ni0.103Mo0.00694V0.00450Nb0.0000602Co0.0877Al0.00892Ti0.00666\\n\",\n        \"output\": \" 1755.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.748C0.00704Mn0.00164Si0.00120Cr0.0218Ni0.0967Mo0.00716V0.000111Nb0.0000606Co0.116Al0.000209\\n\",\n        \"output\": \" 1503.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.714C0.0108Mn0.000102Si0.000400Cr0.0337Ni0.106Mo0.00703V0.000110Nb0.0000605Co0.128Al0.000208Ti0.000117\\n\",\n        \"output\": \" 1818.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.778C0.000465Mn0.000813Si0.00238Cr0.0966Ni0.0808Mo0.0189V0.000110Nb0.0000601Co0.0000947Al0.0186Ti0.00268\\n\",\n        \"output\": \" 1462.7\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \"beginner\",\n        \"output\": \" beginner is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.669C0.00929Mn0.000102Si0.000596Cr0.151Ni0.0000950Mo0.0115V0.000110Nb0.000480Co0.157Al0.000620\\n\",\n        \"output\": \" 1358.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.799C0.000936Mn0.000102Si0.000200Cr0.000108Ni0.170Mo0.00375V0.000110Nb0.0000605Co0.0000954Al0.00167Ti0.0238\\n\",\n        \"output\": \" 1730.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.667C0.00984Mn0.000102Si0.000200Cr0.158Ni0.0000959Mo0.0295V0.00508N0.000804Nb0.0000606Co0.128Al0.00104\\n\",\n        \"output\": \" 1529.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.655C0.00752Mn0.000103Si0.000201Cr0.147Ni0.0000961Mo0.0276V0.00443N0.00161Nb0.0000607Co0.155Al0.000836\\n\",\n        \"output\": \" 1274.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.666C0.00751Mn0.000103Si0.000201Cr0.155Ni0.0000960Mo0.0299V0.00963N0.00161Nb0.0000607Co0.129Al0.00104\\n\",\n        \"output\": \" 1550.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.760C0.000454Mn0.000992Si0.0640Cr0.000105Ni0.172Mo0.000114V0.000107Nb0.0000587Co0.0000925Al0.00101Ti0.00125\\n\",\n        \"output\": \" 1474.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.736C0.0107Mn0.000101Si0.000198Cr0.0964Ni0.0266Mo0.00755V0.00328Nb0.0000600Co0.118Al0.000619Ti0.000349\\n\",\n        \"output\": \" 1522.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.679C0.00705Mn0.000103Si0.000201Cr0.153Ni0.00135Mo0.0282V0.00233Nb0.0000608Co0.128Al0.000628\\n\",\n        \"output\": \" 1341.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.717C0.000960Mn0.000105Si0.000205Cr0.000111Ni0.178Mo0.0288V0.000113Nb0.00186Co0.0665Al0.00192Ti0.00494\\n\",\n        \"output\": \" 1005.9\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.670C0.00798Mn0.000103Si0.000201Cr0.155Ni0.0000961Mo0.0299V0.00454N0.00121Nb0.0000607Co0.131Al0.000627\\n\",\n        \"output\": \" 1502.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.644Mn0.000521Si0.00102Cr0.000110Ni0.177Mo0.0215V0.000112Nb0.0000617Co0.126Al0.00234Ti0.0269\\n\",\n        \"output\": \" 2501.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.686C0.000469Mn0.000410Si0.000802Cr0.107Ni0.0671Mo0.0161Co0.0767W0.00745Al0.0376\\n\",\n        \"output\": \" 1680.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.803C0.000470Mn0.000823Si0.000805Cr0.0511Ni0.117Mo0.0184V0.000111Nb0.0000608Co0.0000959Al0.00544Ti0.00224\\n\",\n        \"output\": \" 1212.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.763C0.00479Mn0.00524Si0.00615Cr0.133Ni0.0196Mo0.000120V0.000113Nb0.0000619Co0.0488W0.0188Al0.000640\\n\",\n        \"output\": \" 1235.9\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.766Mn0.000510Si0.000399Cr0.121Ni0.0945Mo0.0120V0.000110Nb0.0000603Co0.0000950Al0.00270Ti0.00351\\n\",\n        \"output\": \" 1172.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.720C0.00407Mn0.0277Si0.00619Cr0.183Ni0.0411Mo0.000113V0.000107Nb0.0000585Co0.0000923Al0.0181\\n\",\n        \"output\": \" 1236.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength. ->\",\n        \"input\": \" Fe0.750C0.00184Mn0.000101Si0.000394Cr0.133Ni0.0814Mo0.0121V0.000109Nb0.0000596Co0.0000939Al0.0205.\\n\",\n        \"output\": \" Unable to answer due to lack of conditions.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.860C0.0125Mn0.00274Si0.000198Cr0.00439Ni0.0786Mo0.00284V0.000765Nb0.0000600Co0.0369Al0.000619\\n\",\n        \"output\": \" 1139.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.799C0.000470Mn0.000103Si0.000201Cr0.000108Ni0.167Mo0.00847V0.000111Nb0.0000607Co0.0000957Al0.00167Ti0.0224\\n\",\n        \"output\": \" 1392.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.673C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.144Mo0.0149V0.000112Nb0.0000614Co0.145Al0.000635Ti0.0215\\n\",\n        \"output\": \" 1571.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.754C0.00640Mn0.0300Si0.00469Cr0.166Ni0.0387Mo0.000114V0.000108Nb0.0000591Co0.0000931Al0.000610\\n\",\n        \"output\": \" 1153.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.720C0.000948Mn0.000104Si0.000203Cr0.0559Ni0.109Mo0.0303V0.00548Nb0.0000613Co0.0609Al0.00865Ti0.00880\\n\",\n        \"output\": \" 1136.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \"david\",\n        \"output\": \" david is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.735C0.000951Mn0.000104Si0.000203Cr0.0549Ni0.108Mo0.0286V0.000112Nb0.0000615Co0.0601Al0.00190Ti0.00978\\n\",\n        \"output\": \" 1047.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.685C0.0101Mn0.000101Si0.0199Cr0.134Ni0.00884Mo0.0114V0.000108Nb0.000475Co0.129Al0.000614\\n\",\n        \"output\": \" 1383.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.668C0.00972Mn0.00435Si0.00990Cr0.134Ni0.0112Mo0.0119V0.000109Nb0.0000598Co0.150Al0.000618\\n\",\n        \"output\": \" 1352.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.792C0.000470Mn0.000411Si0.00201Cr0.0862Ni0.0980Mo0.0181V0.000111Nb0.0000607Co0.0000957Al0.00167Ti0.000589\\n\",\n        \"output\": \" 1061.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.765C0.000909Mn0.00109Si0.0618Cr0.000105Ni0.170Mo0.000114V0.000107Nb0.0000587Co0.0000926Al0.000607\\n\",\n        \"output\": \" 1419.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.779C0.000946Mn0.000103Si0.000202Cr0.000109Ni0.173Mo0.0184V0.0100Nb0.0000611Co0.0000964Al0.00147Ti0.0166\\n\",\n        \"output\": \" 1730.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.686C0.000910Mn0.0000995Si0.0354Cr0.146Ni0.0475Mo0.000114V0.000107Nb0.0000588Co0.0825Al0.000405Ti0.000457\\n\",\n        \"output\": \" 1226.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.702Mn0.000102Si0.000200Cr0.154Ni0.0802Mo0.0146V0.000110Nb0.0000604Co0.0409Al0.00249Ti0.00551\\n\",\n        \"output\": \" 1274.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.695C0.00971Mn0.000101Si0.00988Cr0.134Ni0.00889Mo0.0115V0.000109Nb0.000478Co0.130Al0.000617\\n\",\n        \"output\": \" 1369.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \"pair\",\n        \"output\": \" pair is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.623C0.00854Mn0.000104Si0.000203Cr0.147Ni0.0000971Mo0.0179V0.00515N0.00163Nb0.0000614Co0.188W0.00729Al0.000845\\n\",\n        \"output\": \" 1123.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.680Mn0.000104Si0.000204Cr0.111Ni0.0680Mo0.0327V0.000112N0.000408Nb0.0000616Co0.106Al0.000636\\n\",\n        \"output\": \" 1373.9\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.711C0.0108Mn0.000102Si0.000200Cr0.0336Ni0.108Mo0.00697V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000117\\n\",\n        \"output\": \" 1777.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.636C0.000474Mn0.000518Si0.00101Cr0.000109Ni0.188Mo0.00860V0.000112Nb0.0000612Co0.144Al0.00274Ti0.0184\\n\",\n        \"output\": \" 2249.6\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.763C0.000466Mn0.000509Si0.000398Cr0.114Ni0.101Mo0.0120V0.000110Nb0.0000602Co0.0000949Al0.00746Ti0.000935\\n\",\n        \"output\": \" 1194.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.655Mn0.000522Si0.00102Cr0.000110Ni0.176Mo0.0215V0.00563Nb0.0000617Co0.117Al0.000425Ti0.0228\\n\",\n        \"output\": \" 2402.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.676C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.180Mo0.0279V0.000112Nb0.0000614Co0.0852Al0.0216Ti0.00846\\n\",\n        \"output\": \" 1309.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.695C0.0106Mn0.000101Si0.0103Cr0.133Ni0.00898Mo0.0114V0.000109Nb0.000478Co0.130Al0.000617\\n\",\n        \"output\": \" 1359.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.818C0.0178Mn0.00194Si0.000200Cr0.0799Ni0.0000958Mo0.0337V0.000662Nb0.0000605Co0.0466Al0.000625\\n\",\n        \"output\": \" 1564.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.785C0.000467Mn0.000511Si0.00180Cr0.0820Ni0.0985Mo0.0178V0.000110Nb0.0000604Co0.0000952Al0.0108Ti0.00235\\n\",\n        \"output\": \" 1383.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.769Mn0.000509Si0.000398Cr0.112Ni0.0953Mo0.0119V0.000110Nb0.0000602Co0.0000949Al0.00725Ti0.00362\\n\",\n        \"output\": \" 1282.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.662C0.000477Mn0.000521Si0.00102Cr0.000110Ni0.168Mo0.0236V0.000112Nb0.0000616Co0.119Al0.00488Ti0.0213\\n\",\n        \"output\": \" 2372.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.803C0.0168Mn0.00215Si0.000200Cr0.0834Ni0.0000957Mo0.0334V0.0127Nb0.0000605Co0.0470Al0.000625\\n\",\n        \"output\": \" 1819.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.696C0.00878Mn0.000101Si0.00989Cr0.135Ni0.00927Mo0.0113V0.000109Nb0.000120Co0.129Al0.000617\\n\",\n        \"output\": \" 1376.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.697C0.00972Mn0.000101Si0.00732Cr0.135Ni0.00909Mo0.0115V0.000109Nb0.000479Co0.130Al0.000618\\n\",\n        \"output\": \" 1332.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.718C0.00317Mn0.00594Si0.00581Cr0.178Ni0.0648Mo0.000113V0.000107Nb0.0000585Co0.0000922Al0.0242\\n\",\n        \"output\": \" 1362.9\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.823C0.0176Mn0.00183Si0.000198Cr0.0779Ni0.0000949Mo0.0219V0.0105Nb0.0000600Co0.0463Al0.000620\\n\",\n        \"output\": \" 1722.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.666C0.00702Mn0.000102Si0.000200Cr0.157Ni0.0000958Mo0.0296V0.00508N0.00602Nb0.0000605Co0.129Al0.00104\\n\",\n        \"output\": \" 1164.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.806C0.0176Mn0.00181Si0.000209Cr0.0802Ni0.0000999Mo0.00153V0.0124Nb0.0000631Co0.0501W0.0293Al0.000652\\n\",\n        \"output\": \" 1681.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.712C0.0103Mn0.000102Si0.000200Cr0.0336Ni0.108Mo0.00698V0.000110Nb0.0000605Co0.129Al0.000208Ti0.000117\\n\",\n        \"output\": \" 1743.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.754C0.00599Mn0.0101Si0.00493Cr0.165Ni0.0396Mo0.0159V0.000109N0.00395Nb0.0000596Co0.0000940Al0.000616\\n\",\n        \"output\": \" 1155.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.690C0.00785Mn0.000101Si0.0154Cr0.134Ni0.00898Mo0.0115V0.000109Nb0.000477Co0.132Al0.000617\\n\",\n        \"output\": \" 1368.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.805C0.000470Mn0.000719Si0.000804Cr0.0496Ni0.116Mo0.0184V0.000111Nb0.0000608Co0.0000958Al0.00711Ti0.00212\\n\",\n        \"output\": \" 1254.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.681C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.181Mo0.0293V0.00439Nb0.0000618Co0.0847Al0.0108Ti0.00779\\n\",\n        \"output\": \" 1164.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.803C0.000460Mn0.000402Si0.0368Cr0.000106Ni0.157Mo0.000115V0.000108Nb0.0000594Co0.0000937Al0.00102Ti0.000923\\n\",\n        \"output\": \" 1188.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \"downtown\",\n        \"output\": \" downtown is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.786C0.000473Mn0.000310Si0.000202Cr0.000109Ni0.175Mo0.0182V0.000112Nb0.0000612Co0.0000965Al0.00190Ti0.0167\\n\",\n        \"output\": \" 1641.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.684C0.00795Mn0.000102Si0.000200Cr0.156Ni0.0000957Mo0.0306V0.00452N0.00481Nb0.0000604Co0.109Al0.00271\\n\",\n        \"output\": \" 1536.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.772C0.0169Mn0.00226Si0.000201Cr0.0732Ni0.0000961Mo0.0338V0.0106Nb0.0000607Co0.0905Al0.000627\\n\",\n        \"output\": \" 1846.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.721C0.000476Mn0.000104Si0.000203Cr0.0560Ni0.109Mo0.0304V0.0105Nb0.0000615Co0.0611Al0.00191Ti0.00931\\n\",\n        \"output\": \" 1040.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.789Mn0.000719Si0.00161Cr0.0814Ni0.101Mo0.0194V0.000111Nb0.0000607Co0.0000957Al0.00439Ti0.00271\\n\",\n        \"output\": \" 1263.6\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.696C0.00925Mn0.000101Si0.000198Cr0.148Ni0.0107Mo0.00573V0.000109Nb0.000538Co0.129Al0.000617\\n\",\n        \"output\": \" 1376.7\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.683C0.00925Mn0.000202Si0.00969Cr0.134Ni0.00890Mo0.0114V0.000109Nb0.000120Co0.142Al0.000618\\n\",\n        \"output\": \" 1258.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.731C0.00897Mn0.000103Si0.000202Cr0.0742Ni0.0271Mo0.0142V0.00312Nb0.0000610Co0.137W0.00401Al0.000631Ti0.000237\\n\",\n        \"output\": \" 1371.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.681C0.00877Mn0.00464Si0.00968Cr0.135Ni0.00898Mo0.00861V0.000109Nb0.0000597Co0.142Al0.000617\\n\",\n        \"output\": \" 1250.8\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.778C0.000931Mn0.000611Si0.00159Cr0.0796Ni0.0981Mo0.0189V0.000110Nb0.0000602Co0.0000949Al0.0189Ti0.00269\\n\",\n        \"output\": \" 1555.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.706C0.0106Mn0.000101Si0.00712Cr0.135Ni0.00899Mo0.0114V0.000109Nb0.000478Co0.120Al0.000617\\n\",\n        \"output\": \" 1302.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.798C0.000469Mn0.000820Si0.00100Cr0.0504Ni0.116Mo0.0184V0.000111Nb0.0000606Co0.0000955Al0.0119Ti0.00235\\n\",\n        \"output\": \" 1390.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.766Mn0.00448Si0.00159Cr0.109Ni0.0981Mo0.0117V0.000110Nb0.0000602Co0.0000949Al0.00622Ti0.00257\\n\",\n        \"output\": \" 1163.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.802C0.000470Mn0.000308Si0.00221Cr0.0518Ni0.117Mo0.0178V0.000111Nb0.0000607Co0.0000958Al0.00544Ti0.00236\\n\",\n        \"output\": \" 1216.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.700C0.000479Mn0.000523Si0.00102Cr0.000111Ni0.170Mo0.0298V0.000113Nb0.0000619Co0.0771Al0.00277Ti0.0180\\n\",\n        \"output\": \" 2356.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.703C0.000908Mn0.0000992Si0.0375Cr0.146Ni0.0557Mo0.000114V0.000107Nb0.0000587Co0.0555Al0.000606Ti0.000569\\n\",\n        \"output\": \" 1130.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.806C0.000468Mn0.0176Si0.000401Cr0.000108Ni0.174Mo0.000117V0.000110Nb0.0000606Co0.0000955Al0.00104Ti0.000705\\n\",\n        \"output\": \" 1136.9\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.768C0.000468Mn0.000512Si0.00180Cr0.0827Ni0.117Mo0.0179V0.000110Nb0.0000605Co0.0000954Al0.00958Ti0.00235\\n\",\n        \"output\": \" 1414.5\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.734C0.00750Mn0.000615Si0.000802Cr0.0211Ni0.0974Mo0.00575V0.000111Nb0.0000606Co0.132Al0.000209Ti0.000118\\n\",\n        \"output\": \" 1629.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.704C0.000476Mn0.000104Si0.000203Cr0.000110Ni0.148Mo0.0304V0.000112Nb0.0000615Co0.0892Al0.0191Ti0.00835\\n\",\n        \"output\": \" 1393.5\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.625Mn0.000102Si0.000200Cr0.0936Ni0.129Mo0.00480V0.000110Nb0.0000604Co0.132Al0.00812Ti0.00669\\n\",\n        \"output\": \" 1736.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.757C0.0186Mn0.00163Si0.000199Cr0.131Ni0.0000953Mo0.0341V0.0105Nb0.0000602Co0.0467Al0.000622\\n\",\n        \"output\": \" 1667.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.714C0.00138Mn0.00602Si0.00589Cr0.154Ni0.0798Mo0.0144V0.000108Nb0.0000593Co0.0000935Al0.0245\\n\",\n        \"output\": \" 1478.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \"shell\",\n        \"output\": \" shell is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.751C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0782Mo0.0128V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0215Ti0.000116\\n\",\n        \"output\": \" 1306.9\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.687Mn0.000102Si0.000199Cr0.119Ni0.0952Mo0.00716V0.000110Nb0.0000601Co0.0712W0.000851Al0.0118Ti0.00689\\n\",\n        \"output\": \" 1729.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.757C0.000465Mn0.000712Si0.00219Cr0.121Ni0.0981Mo0.0119V0.000110Nb0.0000602Co0.0000948Al0.00497Ti0.00269\\n\",\n        \"output\": \" 1157.5\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.733C0.00750Mn0.00164Si0.00100Cr0.0213Ni0.0964Mo0.00587V0.000111Nb0.0000606Co0.133Al0.000209\\n\",\n        \"output\": \" 1592.9\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \"hardhat\",\n        \"output\": \" hardhat is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.735C0.0111Mn0.000101Si0.000198Cr0.0974Ni0.0266Mo0.00754V0.00404Nb0.0000599Co0.117Al0.000619Ti0.000349\\n\",\n        \"output\": \" 1615.8\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.770C0.000930Mn0.00488Si0.00199Cr0.107Ni0.0952Mo0.0112V0.000110Nb0.0000601Co0.0000948Al0.00600Ti0.00245\\n\",\n        \"output\": \" 1188.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.712C0.00471Mn0.00639Si0.00746Cr0.133Ni0.0000964Mo0.0363V0.000111N0.00121Nb0.0000609Co0.0980Al0.000629\\n\",\n        \"output\": \" 1258.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.799C0.000469Mn0.000513Si0.00241Cr0.0520Ni0.117Mo0.0176V0.000111Nb0.0000606Co0.0000956Al0.00835Ti0.00224\\n\",\n        \"output\": \" 1272.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.671C0.00925Mn0.00516Si0.0103Cr0.135Ni0.00965Mo0.0115V0.000109Nb0.0000598Co0.147Al0.000618\\n\",\n        \"output\": \" 1245.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.709C0.0103Mn0.000102Si0.000200Cr0.0328Ni0.107Mo0.00692V0.000110Nb0.0000605Co0.133Al0.000625Ti0.000117\\n\",\n        \"output\": \" 1810.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.808C0.0201Mn0.00214Si0.000200Cr0.0770Ni0.0000955Mo0.0328V0.0112Nb0.0000603Co0.0475Al0.000623\\n\",\n        \"output\": \" 1736.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.696C0.00974Mn0.000101Si0.000198Cr0.150Ni0.0000949Mo0.0116V0.000109Nb0.000480Co0.130Al0.000619\\n\",\n        \"output\": \" 1348.9\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.755C0.00185Mn0.000101Si0.000198Cr0.134Ni0.0794Mo0.0127V0.000109Nb0.0000598Co0.0000942Al0.0158Ti0.000232\\n\",\n        \"output\": \" 1280.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.751C0.00138Mn0.000101Si0.000197Cr0.133Ni0.0784Mo0.0128V0.000109N0.000395Nb0.0000596Co0.0000939Al0.0217Ti0.00104\\n\",\n        \"output\": \" 1357.9\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.777C0.00140Mn0.000102Si0.000199Cr0.122Ni0.0824Mo0.000117V0.000110Nb0.0000603Co0.0000950W0.00561Al0.00810Ti0.00316\\n\",\n        \"output\": \" 1194.0\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.701C0.00750Mn0.000102Si0.000200Cr0.154Ni0.0000959Mo0.0289V0.00508N0.00121Nb0.0000606Co0.101Al0.000835\\n\",\n        \"output\": \" 1405.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.737C0.00836Mn0.000102Si0.000199Cr0.0977Ni0.0266Mo0.00756V0.00318Nb0.0000601Co0.118Al0.000621Ti0.000350\\n\",\n        \"output\": \" 1426.2\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition. ->\",\n        \"input\": \" Fe0.755C0.00185Mn0.000101Si0.000198Cr0.134Ni0.0794Mo0.0127V0.000109Nb0.0000598Co0.0000942Al0.0158Ti0.000232.\\n\",\n        \"output\": \" Unable to answer due to lack of conditions.\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.781C0.000475Mn0.000104Si0.000203Cr0.000110Ni0.173Mo0.0184V0.0112Nb0.0000613Co0.0000967W0.00102Al0.00106Ti0.0131\\n\",\n        \"output\": \" 1688.1\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.677C0.00916Mn0.000100Si0.0294Cr0.134Ni0.00881Mo0.0113V0.000108Nb0.000474Co0.129Al0.000611\\n\",\n        \"output\": \" 1382.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.789C0.00143Mn0.000104Si0.000204Cr0.000110Ni0.181Mo0.000119V0.000112Nb0.0000617Co0.0000972W0.00935Al0.00212Ti0.0168\\n\",\n        \"output\": \" 1600.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.722C0.000475Mn0.000104Si0.000203Cr0.0549Ni0.109Mo0.0297V0.000112Nb0.0000614Co0.0600Al0.00190Ti0.0216\\n\",\n        \"output\": \" 1164.4\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.807C0.000470Mn0.000513Si0.00221Cr0.0501Ni0.116Mo0.0164V0.000111Nb0.0000607Co0.0000957Al0.00439Ti0.00236\\n\",\n        \"output\": \" 1167.2\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.685C0.0116Mn0.000101Si0.000198Cr0.151Ni0.00882Mo0.0116V0.000109Nb0.000479Co0.131Al0.000619\\n\",\n        \"output\": \" 1438.6\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.685C0.00877Mn0.000101Si0.00967Cr0.134Ni0.00907Mo0.00855V0.00359Nb0.0000597Co0.141Al0.000617\\n\",\n        \"output\": \" 1218.4\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.671C0.000470Mn0.000514Si0.00100Cr0.000109Ni0.141Mo0.00882V0.000111Nb0.0000607Co0.147Al0.0159Ti0.0137\\n\",\n        \"output\": \" 2157.3\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.788Mn0.000104Si0.000203Cr0.000109Ni0.176Mo0.0184V0.000112Nb0.0000613Co0.0000966Al0.00105Ti0.0166\\n\",\n        \"output\": \" 1716.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.696C0.00143Mn0.000105Si0.000204Cr0.000110Ni0.180Mo0.0293V0.000113Nb0.0000618Co0.0682Al0.00319Ti0.0212\\n\",\n        \"output\": \" 1233.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.810C0.000940Mn0.000103Si0.000201Cr0.000109Ni0.151Mo0.0118V0.000111Nb0.0000608Co0.0000958Al0.00209Ti0.0234\\n\",\n        \"output\": \" 1723.2\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.774Mn0.000511Si0.000599Cr0.111Ni0.0985Mo0.0120V0.000110Nb0.0000604Co0.0000952Al0.00187Ti0.00105\\n\",\n        \"output\": \" 1032.1\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.765Mn0.000713Si0.00199Cr0.112Ni0.0992Mo0.0128V0.000110Nb0.0000603Co0.0000950Al0.00519Ti0.00281\\n\",\n        \"output\": \" 1224.7\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.671C0.00189Mn0.00569Si0.00547Cr0.134Ni0.0000969Mo0.0347V0.000112N0.00122Nb0.0000612Co0.145Al0.000632\\n\",\n        \"output\": \" 1287.4\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.713C0.00984Mn0.000102Si0.000200Cr0.0335Ni0.107Mo0.00698V0.000110Nb0.0000606Co0.129Al0.000209Ti0.000118\\n\",\n        \"output\": \" 1792.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \"deodorant\",\n        \"output\": \" deodorant is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"What will be the yield strength of given composition at 800-1200 \\u00b0C? ->\",\n        \"input\": \" Fe0.677C0.000478Mn0.000104Si0.000204Cr0.000110Ni0.146Mo0.0188V0.000113Nb0.0000617Co0.149Al0.000638Ti0.00839\\n\",\n        \"output\": \" 1669.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.825C0.0174Mn0.00175Si0.000201Cr0.0565Ni0.0000963Mo0.0344V0.0116Nb0.00554Co0.0468Al0.000628\\n\",\n        \"output\": \" 1860.3\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.751C0.00138Mn0.000101Si0.000197Cr0.134Ni0.0791Mo0.0129V0.000109Nb0.0000596Co0.0000940Al0.0211Ti0.000116\\n\",\n        \"output\": \" 1285.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.732C0.00480Mn0.00556Si0.00533Cr0.136Ni0.0000981Mo0.000120V0.000113N0.00123Nb0.0000620Co0.0953W0.0188Al0.000640\\n\",\n        \"output\": \" 1232.0\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.664C0.00926Mn0.000101Si0.0101Cr0.134Ni0.00900Mo0.0114V0.000109Nb0.000479Co0.161Al0.000618\\n\",\n        \"output\": \" 1322.1\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.666C0.000482Mn0.000105Si0.000206Cr0.000111Ni0.149Mo0.0308V0.000114Nb0.0000623Co0.150Al0.000644Ti0.00242\\n\",\n        \"output\": \" 1580.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \"black\",\n        \"output\": \" black is not a composition and it does not have yield strength.\\n\"\n    },\n    {\n        \"instruction\": \"Given composition, write its potential yield strength at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.751C0.00184Mn0.000101Si0.000197Cr0.133Ni0.0785Mo0.0128V0.000109Nb0.0000596Co0.0000939Al0.0217Ti0.000578\\n\",\n        \"output\": \" 1344.0\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.660C0.000484Mn0.000106Si0.000207Cr0.000112Ni0.148Mo0.0364V0.000114Nb0.0000625Co0.146Al0.000646Ti0.00752\\n\",\n        \"output\": \" 1603.3\\n\"\n    },\n    {\n        \"instruction\": \"Write a possible yield strength of given composition at 800-1200 \\u00b0C. ->\",\n        \"input\": \" Fe0.737C0.000956Mn0.000105Si0.000204Cr0.000110Ni0.127Mo0.0299V0.00530Nb0.0000618Co0.0867Al0.00426Ti0.00852\\n\",\n        \"output\": \" 1061.1\\n\"\n    }\n]"
  },
  {
    "path": "dataset/opv/opv_inverse_design_test.json",
    "content": "[{\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1sc2csc(-c3sc4c(c3F)c(OC)c3scc(F)c3c4OC)c2c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3cc(C)c(-c4cc5cc6sc(-c7sc(-c8sc(-c9sc(C=C(C#N)C(=O)OC)cc9C)cc8C)cc7C)cc6cc5s4)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(-c3cc4c5cccc6c7cccc8c9cc(-c%10ccc%11c(c%10)C(C)(C)c%10ccccc%10-%11)cc%10c%11cccc%12c%13cccc%14c(c3)c4c3c(c65)c(c78)c(c9%10)c(c%12%11)c3c%13%14)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4ccc5ccccc5c4)s3)N(C)C(=O)C2=C1c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc4cc(C=Cc5ccc(C=C(C#N)C(=O)O)s5)sc4c3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c(OC)c(-c2ccc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)s2)c2nsnc2c1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5cc6c(s5)c(-c5ccc(C)s5)c5ccsc5c6-c5ccc(C)s5)s4)c3nc2-c2cccc(OC)c2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3ccc(-c4c5nonc5c(-c5cccs5)c(OC)c4OC)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si]1(C)c2ccsc2-c2sc(-c3cccc4nsnc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4cc5ccccc5c5ccccc45)s3)N(C)C(=O)C2=C1c1ccc(-c2cc3ccccc3c3ccccc23)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2csc(-c3cc(-c4ccc(C)s4)c(-c4ccc(C5=C6C(=O)N(C)C(c7cccs7)=C6C(=O)N5C)s4)s3)c2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2ccc(-c3c4cc(-c5cc(C)c(-c6ccc(-c7sc(C=C8SC(=S)N(C)C8=O)cc7C)s6)s5)sc4c(-c4ccc(-c5ccc(C)s5)s4)c4cc(-c5cc(C)c(-c6ccc(-c7sc(C=C8SC(=S)N(C)C8=O)cc7C)s6)s5)sc43)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(C=C2C(=O)c3ccccc3C2=O)sc1-c1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(C6=S=C(C=C7C(=O)c8ccccc8C7=O)C=C6C)cc5C)cc4C)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5c4=NC(c4ccccc4)C(c4ccccc4)N=5)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc3c(c2)C(C)(C)c2c-3c3c(c4c2-c2ccc(N(c5ccc(OC)cc5)c5ccc(OC)cc5)cc2C4(C)C)-c2ccc(-c4ccc(C=C(C#N)C(=O)O)s4)cc2C3(C)C)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" c1csc(-c2cc(-c3cccs3)c(-c3cccs3)s2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1sc(-c2sc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc2C)c2nc3c4ccccc4c4ccccc4c3nc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(C(C#N)=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si]1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2ccc(-c3ncc(-c4cc5c(s4)-c4sc(-c6cnc(-c7ccc(-c8ccc(C)s8)s7)c7nsnc76)cc4[Si]5(C)C)c4nsnc43)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4cnc(-c5cccs5)c5nccnc45)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71B, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3cc(-c4ccc(-c5sc(-c6cccs6)c6c5C(=O)c5c(C)sc(C)c5C6=O)s4)sc3c(-c3ccc(C)s3)c3ccsc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3sc(C=C(C#N)C(=O)O)c4c3OCCO4)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(C=C2C(=O)N(C)C(=O)N(C)C2=O)sc1-c1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(C6=S=C(C=C7C(=O)N(C)C(=O)N(C)C7=O)C=C6C)cc5C)cc4C)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1ccc2c3ccccc3n(-c3ccc(OC)cc3)c2c1\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc(-c2nc(C)c(-c3ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s3)s2)sc1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2cc(-c3cc4c(s3)-c3sc(C=C(C#N)C(=O)O)cc3C4(C)C)ccc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2c(csc2-c2cc3c(s2)c(OC)c2ccsc2c3OC)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(C3c4ccccc4-c4ccc(-c5ccc(-c6c7nsnc7c(-c7cccs7)c7nc(-c8ccccc8)c(-c8ccccc8)nc76)s5)cc43)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2sc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc2cc2c1cc1cc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)sc1c2OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4cnc(-c5cccs5)c5nonc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4cc5c(s4)-c4sc(-c6cc(C)c(-c7ccc(C8=S=C(C=C(C#N)C(=O)OC)C=C8C)s7)s6)cc4[Si]5(C)C)cc3C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5cccs5)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(C#N)=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=C(C#N)C#N)s4)cc3)c3ccc(-c4ccc(C=C(C#N)C#N)s4)cc3)cc2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(-c2ccc(-c3cc(C)c(-c4cccs4)s3)c3nsnc32)sc1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CSc1ccc(-c2ccc(-c3csc(-c4cc(-c5ccc(-c6ccc(SC)s6)s5)sc4-c4sc(-c5ccc(-c6ccc(SC)s6)s5)cc4-c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)c3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3cc(C)c(-c4nc5sc(-c6sccc6C)nc5s4)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1sccc1C(=O)OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3sc(-c4ccc(-c5cc(C)cs5)c5nsnc54)cc3C)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1sc2c(-c3ccc(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)s3)sc(-c3cccs3)c2c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(-c2cc(-c3ccc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)c(-c3ccc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)s2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2sc(-c3ccc(-c4cc(C)c(-c5cc(C)c(-c6ccc7c8cc9c(cc8n(C)c7c6)c6ccccc6n9C)s5)s4)c4nsnc43)cc2C)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1ccc(-c2sc(-c3nc(C)c(-c4ccc(C5=S=C(c6cc7c(s6)-c6sccc6[Si]7(C)C)C=C5C)s4)s3)nc2C)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2nc3cccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5cc(-c7cccs7)ccc5-6)s4)c3nc2-c2ccc(C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(C#N)=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)cc2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4ccc(C(F)(F)F)cc4)s3)N(C)C(=O)C2=C1c1ccc(-c2ccc(C(F)(F)F)cc2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2nc3sc(-c4cc(C)c(-c5cc6c(s5)-c5sccc5[Si]6(C)C)s4)nc3s2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(C5=C(c6ccccc6)C(c6ccccc6)=C(c6ccc(-c7cccs7)s6)[Si]5(C)C)s4)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2c1=S=C(c1cc(C)c(-c3sc(-c4nc(C)c(-c5sccc5C)s4)nc3C)s1)C=2\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)s4)c3nc2-c2ccc(OC)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC(=O)c1cc2csc(-c3cc4c(s3)c(-c3ccc(C)s3)c3ccsc3c4-c3ccc(C)s3)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC(=O)c1cc2c(csc2-c2cc3c(s2)c2sccc2c(C)c3C)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c(OC)c(-c2cc3sc(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)cc3s2)c2nsnc2c1-c1cc2sccc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1csc2c1C(C)(C)c1cc(-c3scc4c3C(=O)N(C)C4=O)sc1-2\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4ccccc4)s3)N(C)C(=O)C2=C1c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(-c3ccc(N(c4ccccc4)c4ccc(C=Cc5ccc(C=C(C#N)C#N)s5)cc4)cc3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1ccc(-c2sc(-c3ccc4c(c3)N(C)C(=O)C4=C3c4ccccc4N(C)C3=O)cc2C)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccsc2-c2sc(-c3cccc4nsnc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(C#Cc2ccc(C#Cc3ccc(-c4ccc(-c5ccc(C#Cc6ccc(C#Cc7ccc(OC)c(OC)c7)cc6)s5)c5nsnc54)s3)cc2)cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4cccs4)s3)N(C)C(=O)C2=C1c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(-c4ccc(C=C(C#N)C#N)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4cccs4)o3)N(C)C(=O)C2=C1c1ccco1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(C=C(c2ccc(N(c3ccccc3)c3ccccc3)cc2)c2ccc(N(c3ccccc3)c3ccccc3)cc2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2c1=S=C(c1ccc(-c3sc(-c4nc(C)c(-c5cccs5)s4)nc3C)s1)C=2\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(C=Cc3ccc(C=C(C#N)C(=O)O)s3)cc2)c2ccc(OC)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1ccc(N(c2ccccc2)c2ccc(C=C3SC(=S)N(CC(=O)O)C3=O)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(-c2c3cc(-c4cccs4)sc3c(-c3cc(C)c(C)s3)c3cc(-c4ccc(-c5ccc6c(c5F)N(C)C(=O)C6=C5c6cccc(F)c6N(C)C5=O)s4)sc32)sc1C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c4sccc4c4cc(C)c(C)cc54)s3)c3nsnc32)c1\\n\"}]"
  },
  {
    "path": "dataset/opv/opv_inverse_design_train.json",
    "content": "[{\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2csc(-c3cccs3)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccsc1-c1sc(-c2scc3c2C(=O)N(C)C3=O)cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3cc(C)c(-c4sc(-c5sccc5C)c5c4C(=O)N(C)C5=O)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COCc1cc2csc(-c3cc4c(s3)c(OC)c3ccsc3c4OC)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5ccc(C6=C(c7ccccc7)C(c7ccccc7)=C(c7ccc(-c8ccc(C9=S=CC=C9)s8)s7)[Si]6(C)C)s5)s4)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2csc(-c3cc4c(s3)c(C)c3ccsc3c4C)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1sc2c(-c3ccc(-c4cc5c(s4)c(-c4ccc(OC)cc4)c4ccsc4c5-c4ccc(OC)cc4)s3)sc(-c3cccs3)c2c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(C=Cc4ccc(C(F)(F)F)cc4)s3)N(C)C(=O)C2=C1c1ccc(C=Cc2ccc(C(F)(F)F)cc2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1C1=NC2SC(c3sc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)cc3C)=NC2S1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2csc(-c3ccc(-c4ccc(-c5sccc5C)s4)s3)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccsc2-c2sc(-c3c4nsnc4cc(F)c3F)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1sc2c(-c3ccc(-c4cc5c(s4)c(-c4cc(F)c(C)s4)c4ccsc4c5-c4cc(F)c(C)s4)s3)sc(-c3cccs3)c2c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3cc4sc(-c5cccs5)cc4s3)N(C)C(=O)C2=C1c1cc2sccc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(C=CC=C(C#N)C(=O)O)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" O=C1c2ccccc2C(=O)C1=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)cc2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C#Cc1cc2c(s1)-c1sc(C#Cc3scc4nc(-c5ccccc5)c(-c5ccccc5)nc34)cc1C2(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3sc4cc(-c5scc6cc(S(C)(=O)=O)sc65)sc4c3c(-c3ccc(C)s3)c3sc4ccsc4c32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2ccc(C3=C4C(=O)N(C)C(c5ccc(-c6cc(C)cs6)s5)=C4C(=O)N3C)s2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2ccc(-c4nnc(-c5cccs5)nn4)s2)cc1C3(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c(OC)c(-c2ccc(-c3cc4c(s3)c(-c3ccc(C)s3)c3ccsc3c4C3=S=C(C)C=C3)s2)c2nsnc2c1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1ccc2c3ccc(C=Cc4sc(-c5ccc(-c6ccc(-c7cc(C)cs7)s6)s5)cc4C)cc3n(-c3ccc(OC)cc3)c2c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nccnc45)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cc(OC)cc(-c2nc3c(nc2-c2cc(OC)cc(OC)c2)c(-c2cccs2)sc3-c2cccs2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3cc(-c4sc5cc(-c6ccc(-c7csc8c(C)csc78)c7nsnc76)sc5c4C)sc3c(-c3ccc(C)s3)c3ccsc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2cccc4nsnc42)cc1C3(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CSc1ccc(-c2ccc(-c3ccc([Si](c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)(c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2csc(-c3cc4c(s3)c(OC)c3ccsc3c4OC)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2cc3c4nsnc4c(-c4cc(C)c(-c5cc6c(s5)c(-c5cc(C)c(C)s5)c5ccsc5c6C5=S=C(C)C(C)=C5)s4)cc3c3nsnc32)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=5 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1cc(C#N)c(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1C#N)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(-c5ccc(C=C(C#N)C(=O)O)s5)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(N(c2ccccc2)c2ccccc2)cc1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2sccc2c2cc(-c3cc(C)c(-c4nc5sc(-c6sccc6C)nc5s4)s3)sc2c1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(C=C(C#N)C(=O)O)sc1-c1cc(C)c(-c2cc(C)c(-c3cc4ccc(N(c5ccc6c(c5)C(C)(C)c5ccccc5-6)c5ccc6c(c5)C(C)(C)c5ccccc5-6)cc4s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2csc(-c3cc4c(s3)c(-c3ccc(C)s3)c3ccsc3c4-c3ccc(C)s3)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3cc4c(s3)-c3sc(C=C(C#N)C(=O)O)cc3C4(C)C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(-c2nc3c(nc2-c2ccc(OC)cc2)c(-c2ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s2)sc3-c2cccs2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C(=Cc1cccc2nsnc21)c1ccc(N(c2ccc(C=Cc3cccc4nsnc43)cc2)c2ccc(C=Cc3cccc4nsnc43)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1ccc(-c2ccc(-c3sccc3C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=CC=Cc1ccc(N(c2ccccc2)c2ccccc2)cc1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2nnc(-c3cc(C)c(-c4cc5c(s4)-c4sccc4[Si]5(C)C)s3)nn2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" c1csc(-c2ccsc2-c2cccs2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(C=C(C#N)c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3cc(-c4ccc(-c5sc(-c6cccs6)c6cc(S(C)(=O)=O)sc65)s4)sc3c(-c3ccc(C)s3)c3ccsc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)CC(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)=CC(=C(C#N)C(=O)O)C1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3ccc(-c4ccc(C=C(C#N)C(=O)O)s4)s3)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC(=O)c1sc2csc(-c3cc4c(s3)c(C)c3ccsc3c4C)c2c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(-c2nc3c(-c4scc5c4OCCO5)ccc(-c4sc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)c5c4OCCO5)c3nc2-c2ccc(OC)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1ccc2c3ccc(C=Cc4cccs4)cc3n(-c3ccc(OC)cc3)c2c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccsc1-c1ccc(-c2sc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc2OC)c2nsnc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c(OC)c(-c2ccc(-c3ccc4c5ccccc5n(C)c4c3)s2)c2nsnc2c1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2sc(-c3cc(C)c(-c4cccs4)s3)c3sc(C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc23)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1nc2sc(-c3sc(-c4ccc5c6ccccc6n(C)c5c4)cc3C)nc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2c3nsnc3c(-c3cc(C)c(-c4cc5c(s4)c(C)c4ccsc4c5C)s3)c(F)c2F)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1c2ccsc2c(C)c2cc(-c3ccc(-c4cnc(-c5cccs5)c5nsnc54)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC(=O)c1cc2c(csc2-c2cc3c(s2)c(C)c2ccsc2c3C)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=5 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1cc(OC)c(C=Cc2cc(C=C(C#N)c3ccc([N+](=O)[O-])cc3)ccc2C=C(C#N)c2ccc([N+](=O)[O-])cc2)cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc2c3cc(C)sc3c3nc4c(-c5ccc(-c6ccc7c8ccccc8n(C)c7c6)s5)ccc(-c5cccs5)c4nc3c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2cc3c(cc21)-c1cc2c(cc1C3(C)C)-c1ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc1C2(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2ccc(-c4ccc(-c5cccs5)c5nsnc54)s2)cc1C3(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-n2c(-c3ccsc3)nc3c2c2ccc(C)cc2c2cc(C)ccc32)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1sc2c(csc2-c2cc3c(s2)c(OC)c2ccsc2c3OC)c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2c1=S=C(c1cc(C)c(-c3ccc(-c4sc(-c5nc(C)c(-c6ccc(-c7sccc7C)s6)s5)nc4C)s3)s1)C=2\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1=CC(c2ccc(-c3cc(C)c(-c4cc5c(s4)c4sccc4c4nc(C)c(C)nc54)s3)c3nsnc32)=S=C1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2cc3c4nsnc4c(-c4cc(C)cs4)cc3c3nsnc32)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3scc4sc(S(C)(=O)=O)cc43)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc(N(c2ccccc2)c2ccccc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2nc3c(nc2-c2ccc(C)cc2)c(-c2ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s2)sc3-c2cccs2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(C=Cc3cc4c(s3)-c3sc(C=C(C#N)C(=O)O)cc3C4(C)C)cc2)c2ccc(OC)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cccc5nc6c7ccsc7c7sccc7c6nc53)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccsc2c2sc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c(OC)c(-c2ccc(-c3ccc(-c4ccc5c6ccccc6n(C)c5c4)s3)s2)c2nsnc2c1-c1ccc(-c2cccs2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)s4)c3nc2-c2cccc(OC)c2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3ccc4ccc5cccc6ccc3c4c56)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(C=C(C#N)C#N)sc2-c2sc(C=C(C#N)C#N)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(C=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(-c2c3ccsc3c(-c3cc(C)c(C)s3)c3cc(-c4ccc5c(c4)N(C)C(=O)C5=C4c5ccccc5N(C)C4=O)sc32)sc1C\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc2c(c1)C(C)(C)c1cc(N(c3ccccc3)c3cccc4ccccc43)ccc1-2\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(C(C#N)=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc2c(c1)c1cc(N(c3ccccc3)c3ccccc3)ccc1n2C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(-c4ccc(C)cc4)c4ccsc4c5-c4ccc(C)cc4)s3)c3nsnc32)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C#Cc1cc(OC)c(C#Cc2scc3nc(-c4ccccc4)c(-c4ccccc4)nc32)cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C#Cc1cc2c(s1)c1sc(C#Cc3cccc4nsnc43)cc1n2C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4nnc(-c5cccs5)c5nonc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5ccc(-c6cccs6)c6nsnc65)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(-c2cc(C)c(C3=S=CC=C3)s2)sc1-c1ccc(-c2cccc3nsnc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c(-c2ccc(C=C(C#N)C(=O)O)cc2)ccc1-c1ccc(N(c2ccccc2)c2ccccc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" c1csc(-c2ccc(-c3ccc(-c4c(-c5ccc(-c6cccs6)s5)sc(-c5ccc(-c6cccs6)s5)c4-c4ccc(-c5ccc(-c6cccs6)s5)s4)s3)s2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(OCCCCCCOc2ccc(C=C(C#N)c3ccc([N+](=O)[O-])cc3)cc2O)c(O)c1)c1ccc([N+](=O)[O-])cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(C#Cc4cc5ccccc5c5ccccc45)s3)N(C)C(=O)C2=C1c1ccc(C#Cc2cc3ccccc3c3ccccc23)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4cc5sc(C=C(C#N)C(=O)O)cc5s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1sc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)c2c1OCCO2)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccsc2-c2sc(-c3ccc(-c4nc5sc(-c6cccs6)nc5s4)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(C)sc2c(OC)c2cc(-c3ccc(-c4sc(-c5ccc(C)s5)c5c4C(=O)N(C)C5=O)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)CC(C=Cc2ccc(N(c3ccc(N(c4ccccc4)c4ccccc4)cc3)c3ccc(N(c4ccccc4)c4ccccc4)cc3)cc2)=CC(=C(C#N)C(=O)O)C1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3c4ccccc4cc4ccccc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C#Cc1cc2c(s1)c1sc(C#Cc3scc4nc(-c5ccccc5)c(-c5ccccc5)nc34)cc1n2C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1c2ccccc2C(=C2c3ccc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)cc3N(C)C2=O)C1=O\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(C=C(C#N)C(=O)O)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc2c(nc1C)c(-c1ccc(-c3ccc4c5ccccc5n(C)c4c3)s1)sc2-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si]1(C)c2cc(-c3cnc(-c4cccs4)c4nsnc43)sc2-c2sc(-c3cnc(-c4cccs4)c4nsnc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C(=C1Sc2ccccc2S1)c1ccc(N(c2ccc(C=C3Sc4ccccc4S3)cc2)c2ccc(C=C3Sc4ccccc4S3)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2ccc(-c3cc(C)cs3)c3nsnc32)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(C)c(-c2c3cc(-c4ccc(-c5ccc(-c6cccs6)c6nsnc65)s4)sc3c(-c3sc(C)cc3C)c3ccsc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(C)cc(-c2ccc(N(c3ccc(-c4cc5c(s4)-c4sc(C=C(C#N)C(=O)O)cc4C5(C)C)cc3)c3ccc(-c4cc(C)cc(C)c4)cc3)cc2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4ccc5c(c4)C(C)(C)c4cc(-c6cc(C)c(-c7ccc(-c8sc(C=C(C#N)C(=O)OC)cc8C)s7)s6)ccc4-5)cc3C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4nnc(-c5cccs5)c5nccnc45)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1cc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)c(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2ccc(-c3ccc(-c4ccc(N(c5ccc(-c6ccc(-c7ccc(-c8ccc(C)s8)s7)s6)cc5)c5ccc(-c6ccc(-c7ccc(-c8ccc(C)s8)s7)s6)cc5)cc4)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2sc(-c3nc4cc5sc(-c6cc(C)c(-c7cc(C)cs7)s6)nc5cc4s3)cc2C)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2cc3c(cc21)-c1ccc(-c2ccc(-c4ccc(-c5cccs5)c5nsnc54)s2)cc1C3(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COCc1sc2c(csc2-c2cc3c(s2)c(OC)c2ccsc2c3OC)c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C#Cc1sc(C#Cc2scc3nc(-c4ccccc4)c(-c4ccccc4)nc23)c(C)c1C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5ccc(C6=C7C(=O)N(C)C(c8cccs8)=C7C(=O)N6C)s5)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc(-c2ccc3c(c2)C(C)(C)c2cc(N(c4ccccc4)c4ccccc4)ccc2-3)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3sc(C4=S=Cc5ccccc54)c4ccccc43)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c7ccccc7n(C)c6c5)s4)c3nc2-c2ccc(OC)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)Oc2cc(-c3c4nsnc4cc(F)c3F)sc2-c2sccc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)sc1-c1nc2sc(-c3sc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)cc3C)nc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(-c5ccc(C=CC=C(C#N)C(=O)O)s5)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1ccc(N(c2ccccc2)c2ccc(-c3ccc(C=C4SC(=S)N(CC(=O)O)C4=O)s3)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(-c2ccc(-c3ccc(C=C(C#N)c4ccc([N+](=O)[O-])cc4)s3)c3c2C(=O)OC3=O)s1)c1ccc([N+](=O)[O-])cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)s3)c3nsnc32)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si]1(C)c2ccsc2-c2sc(-c3nc4sc(-c5cc6c(s5)-c5sc(-c7cc8sccc8s7)cc5[Si]6(C)C)nc4s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(C=C(C#N)C(=O)OC)cc5C)cc4C)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(-c4ccc(C=C(C#N)C(=O)O)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3cccc4ccccc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1=CC(c2cc(C)c(-c3sc(-c4cc(C)c(-c5nc6scnc6s5)s4)cc3C)s2)=S=C1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1nc2sc(-c3sc(-c4cc5c(s4)c(C#C[Si](C)(C)C)c4ccsc4c5C#C[Si](C)(C)C)cc3C)nc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(C=Cc3sc(C=C(C#N)C(=O)O)c4c3OCCO4)cc2)c2ccc(OC)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1cc(OC)ccc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3scc4c3C(=O)N(C)C4=O)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(C(=Cc3ccc(C=C(C#N)C(=O)O)s3)c3ccc(N(c4ccc(OC)cc4)c4ccc(OC)cc4)cc3)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3ccsc3c(-c3ccc(C)s3)c3cc(-c4ccc(C5=C6C(=O)N(C)C(c7cccs7)=C6C(=O)N5C)s4)sc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(C=Cc2ccc(C=Cc3cc(OC)c(C=Cc4ccc(C=Cc5cc(OC)c(C=Cc6ccc(C=Cc7cc(OC)c(C=O)cc7OC)s6)cc5OC)s4)cc3OC)s2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(-c3ccc(C4=C(c5ccccc5)C(c5ccccc5)=C(c5cccs5)[Si]4(C)C)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc(-c2nc(C)c(-c3ccc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)s3)s2)sc1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)sc1-c1cnc(-c2ncc(-c3sc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)cc3C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(C#Cc2ccc(-c3ccc(-c4ccc(C#Cc5ccc(OC)c(OC)c5)s4)c4nsnc43)s2)cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccsc2c2sc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc(-c2nc(C)c(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)sc1-c1ccc(N(c2ccccc2)c2ccccc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3cc(-c4cc5sc(C6=C7C(=O)N(C)C(c8cc9sccc9s8)=C7C(=O)N6C)cc5s4)sc3c(-c3ccc(C)s3)c3ccsc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4sc(-c5cccs5)c5nc(-c6ccccc6)c(-c6ccccc6)nc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2c(csc2-c2sc3c(c2F)c(OC)c2scc(F)c2c3OC)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)s3)N(C)C(=O)C2=C1c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3sc(-c4scc5c4C4C=CC5CC4(C)C)c4c3C3C=CC4C(C)(C)C3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(C=C2C(=O)c3ccccc3C2=O)sc1-c1cc(C)c(-c2ccc(-c3sc(C4=S=C(C=C5C(=O)c6ccccc6C5=O)C=C4C)cc3C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1cc(OC)c(C=Cc2ccc(N(c3ccccc3)c3ccc(C=C(C#N)c4ccc([N+](=O)[O-])cc4)cc3)cc2)cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)c2csc(-c3cc4c(s3)-c3sccc3[Si]4(C)C)c2C1=O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1=CC(c2cc(C)c(-c3ccc(-c4sc(-c5nc(C)c(-c6cccs6)s5)nc4C)s3)s2)=S=C1\\n\"}, {\"instruction\": \"Design a donor with acceptor Tio2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2c1c1c(c3c2C(C)(C)c2cc(N(c4ccccc4)c4ccccc4)ccc2-3)C(C)(C)c2cc(N(c3ccccc3)c3ccccc3)ccc2-1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3ccsc3c(-c3ccc(C)s3)c3cc(-c4scc5cc(S(C)(=O)=O)sc54)sc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C(=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)cc2)s1)c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3cccc4ccccc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si](C)(C)C#Cc1c2ccccc2c2ccc3c(C#C[Si](C)(C)C)c4ccccc4c4ccc1c2c34\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1c(-c2cccs2)sc2c(C)c(-c3ccc(-c4scc5c4C(=O)N(C)C5=O)s3)sc12\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2ccc(-c3cc(F)c(-c4cc5c(s4)-c4sc(-c6c7nsnc7c(-c7ccc(-c8ccc(C)s8)s7)cc6F)cc4[Si]5(C)C)c4nsnc43)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3scc4sc(C(C)=O)cc43)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PDI, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccccc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5cc6c7c8c(cccc8CCc7c5)n6C)s4)c3nc2-c2ccc(OC)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3scc4sc(C(C)=O)c(F)c43)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(-c2cc3c4nsnc4c(-c4cc(C)c(-c5cccs5)s4)cc3c3nsnc32)sc1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1c2ccccc2C(=C2c3ccc(-c4cccs4)cc3N(C)C2=O)C1=O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(C#Cc2c3ccccc3c(C#Cc3ccc(OC)c(OC)c3)c3ccccc23)cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1c2cc(-c3ccc(-c4c5nn(C)nc5c(-c5cccs5)c(F)c4F)s3)sc2c(C)c2ccsc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2cc(-c3ccc(C)s3)c(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)s2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2cccc(-n3c4ccccc4c4ccc(-c5ccc(-c6c7nsnc7c(-c7cccs7)c7nc(-c8ccccc8)c(-c8ccccc8)nc76)s5)cc43)c2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3cc4sccc4s3)N(C)C(=O)C2=C1c1cc2sccc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(-c3cc(C)c(-c4ccc(-c5sc(C=C6SC(=S)N(C)C6=O)cc5C)s4)s3)sc2c(OC)c2cc(-c3cc(C)c(-c4ccc(-c5sc(C=C6SC(=S)N(C)C6=O)cc5C)s4)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3ccc(-c4sc(-c5cccs5)c5c4C(=O)N(C)C5=O)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc2cc3c(C#C[Si](C)(C)C)c4cc5sc(C)cc5cc4c(C#C[Si](C)(C)C)c3cc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2ccc(-c4nc5sc(-c6cccs6)nc5s4)s2)cc1C3(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4cc5c(s4)-c4sccc4C5(C)C)s3)N(C)C(=O)C2=C1c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s3)N(C)C(=O)C2=C1c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2sccc2c2cc(-c3ccc(-c4sc(-c5nc(C)c(-c6cccs6)s5)nc4C)s3)sc2c1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc2c(-c3cccs3)nnc(-c3ccc(-c4ccc5c6ccccc6n(C)c5c4)s3)c2nc1C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2cc3c(cc21)-c1ccc(-c2ccc(-c4ccc(-c5cccs5)c5c4=NC(c4ccccc4)C(c4ccccc4)N=5)s2)cc1C3(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(C=Cc2ccc(C=Cc3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3ccc(C=C(C#N)C(=O)O)s3)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c(-c2ccc(-c3cccc4nsnc43)s2)ccc1C1=S=CC=C1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(-c3cc4c(s3)-c3sc(C5=NC6SC(c7cc8c(s7)-c7sccc7[Si]8(C)C)=NC6S5)cc3[Si]4(C)C)sc2c(OC)c2ccsc21\\n\"}, {\"instruction\": \"Design a donor with acceptor ICBA, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(-c3cc4c(s3)-c3sc(-c5nc6sc(-c7cc8c(s7)-c7sccc7[Si]8(C)C)nc6s5)cc3[Si]4(C)C)sc2c(OC)c2ccsc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cccs3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1sc(-c2sc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc2C)c2nc3c(nc21)-c1cccc2cccc-3c12\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4ccc5c6ccc(-c7cc(C)c(-c8ccc(-c9sc(C=C(C#N)C(=O)OC)cc9C)s8)s7)cc6n(C)c5c4)cc3C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4cc5sc6cc(C=C(C#N)C(=O)O)sc6c5s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nonc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cccc2c1ccc(-c1ccc(-c3ccc(-c4cccs4)c4nsnc43)s1)c2OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc2c3ccsc3c3sc(-c4ccc(-c5cnc(C6=S=CC=C6)c6nsnc65)s4)cc3c2nc1C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1sc(-c2sc(C3=S=C(c4sccc4C)C=C3C)cc2C)c2nc3c4ccccc4c4ccccc4c3nc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3cc(C)c(-c4ccc(-c5sc(-c6sc(-c7sc(C=C(C#N)C(=O)OC)cc7C)cc6C)cc5C)s4)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=CC1=S=C(c2cc(C)c(-c3ccc(-c4sc(-c5sc(-c6ccc(-c7cc(C)c(-c8cc(C)c(-c9ccc(-c%10sc(C%11=S=C(C=C(C#N)C(=O)OC)C=C%11C)cc%10C)s9)s8)s7)c7nsnc76)cc5C)cc4C)s3)s2)C(C)=C1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1nnc(-c2sc(-c3cc4c(s3)-c3sccc3C4(C)C)cc2C)nn1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc2c(c1)C(C)(C)c1cc(N(c3ccccc3)c3ccccc3)ccc1-2\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4cc5c(s4)c(OC)c4cc(-c6cc(C)c(-c7ccc(-c8sc(C=C(C#N)C(=O)OC)cc8C)s7)s6)sc4c5OC)cc3C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(C=C(C#N)C(=O)O)sc2-c2sc(-c3ccc(N(c4ccc(N5c6ccccc6Sc6ccccc65)cc4)c4ccc(N5c6ccccc6Sc6ccccc65)cc4)cc3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2nnc(-c3cc(C)c(-c4cc5c(s4)-c4sccc4C5(C)C)s3)nn2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc(-c2nc(C)c(-c3ccc(C4=S=C5c6cc7c(cc6C(C)(C)C5=C4)-c4sccc4C7(C)C)s3)s2)sc1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5ccc(-c6ccc(-c7ccc(-c8cccs8)s7)c7nsnc76)s5)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3scc4cc(C(C)=O)sc43)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3ccc(C=C(C#N)C(=O)O)o3)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cccc5nsnc53)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc(C=C(C#N)c4ccc(C=C(C#N)C(=O)O)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2ccc(-c3cnc(-c4cc5c(s4)-c4sc(-c6ncc(-c7ccc(-c8ccc(C)s8)s7)c7nsnc76)cc4[Si]5(C)C)c4nsnc43)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1cc(C)c(-c2ccc(-c3cc(C)c(C4=S=C(c5ccc6c7cc8c(cc7n(C)c6c5)c5ccccc5n8C)C(C)=C4)s3)c3nsnc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si]1(C)c2ccsc2-c2sc(-c3cccc4nonc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2c1=S=C(c1sc(-c3sc(-c4nc(C)c(-c5cc(C)cs5)s4)nc3C)cc1C)C=2\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1c2ccccc2Sc2cc(C=Cc3ccsc3-c3cccs3)ccc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cc2c3ccsc3c3sc(-c4sc(-c5ccc(-c6cc(C)cs6)c6nsnc65)cc4C)cc3c2cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc(-c2nc(C)c(-c3ccc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)s2)sc1-c1ccc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cc2c3ccsc3c3sc(-c4cccc5nsnc54)cc3c2cc1OC\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4cc5ccccc5o4)s3)N(C)C(=O)C2=C1c1ccc(-c2cc3ccccc3o2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1ccc2c3ccc(C=Cc4ccc(-c5ccc(C6=C(C)C(C)=C(c7ccc(-c8cccs8)s7)S6(=O)=O)s5)s4)cc3n(-c3ccc(OC)cc3)c2c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C=Cc1ccc2c3ccc(C=Cc4sc(-c5cc(C)cs5)cc4C)cc3n(-c3ccc(OC)cc3)c2c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(C#N)=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=C(C#N)C#N)s4)cc3)cc2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc2c3ccsc3c3sc(-c4ccc(-c5cnc(-c6cccs6)c6nsnc65)s4)cc3c2cc1C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1sc2csc(-c3cc4c(s3)c(OC)c3ccsc3c4OC)c2c1F\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc(-c2nc(C)c(-c3ccc(C4=S=C5c6sccc6C(C)(C)C5=C4)s3)s2)sc1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3sc(-c4cc5sc(C=C(C#N)C(=O)O)cc5s4)c4c3OCCO4)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccc(C=C(C#N)C#N)cc2c2cc(C=C(C#N)C#N)ccc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c7ccccc7n(C)c6c5)s4)c3nc2-c2ccc(C)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(-c2ccc(-c3ccc(C=C(C#N)c4ccc([N+](=O)[O-])cc4)s3)c3c2C(=O)N(c2ccc(C(=O)O)cc2)C3=O)s1)c1ccc([N+](=O)[O-])cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(-c4cc(C)c(C)s4)c4ccsc4c5-c4cc(C)c(C)s4)s3)c3nsnc32)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2sc(-c3ccc(-c4ccc(N(c5ccc(-c6ccc(-c7sc(-c8ccc(C)s8)c8c7OCCO8)s6)cc5)c5ccc(-c6ccc(-c7sc(-c8ccc(C)s8)c8c7OCCO8)s6)cc5)cc4)s3)c3c2OCCO3)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)sc2c(OC)c2ccsc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(-c3cccs3)sc2c(OC)c2cc(-c3ccc(-c4ccc5c(c4)N(C)C(=O)C5=C4c5ccccc5N(C)C4=O)s3)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(-c6cc7c(s6)c(OC)c6cc(-c8cc(C)c(-c9cc(C)c(-c%10ccc(-c%11sc(-c%12sc(C=C(C#N)C(=O)OC)cc%12C)cc%11C)s%10)s9)s8)sc6c7OC)cc5C)cc4C)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2c(-c3cccs3)sc(-c3ccc(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)s3)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2ccc(-c3ccc(C4=C5C(=O)N(C)C(c6ccc(-c7ccc(C8=S=C(C)C=C8)s7)s6)=C5C(=O)N4C)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C(=Cc1ccc(N(c2ccccc2)c2ccccc2)cc1)c1ccc(-c2ccc(-c3ccc(C=Cc4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)c3nsnc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(-c3cccs3)sc2c(OC)c2ccsc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2cc(C)c(-c3scc4c3C(=O)N(C)C4=O)s2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3cc(-c4ccc(C5=C6C(=O)N(C)C(c7cccs7)=C6C(=O)N5C)s4)sc3c(-c3ccc(C)cc3)c3ccsc32)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(-c4ccc(-c5ccc(C=C(C#N)C#N)s5)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)c2csc(-c3cc4c(s3)-c3sccc3C4(C)C)c2C1=O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(-c2c3ccsc3c(-c3ccc(C)s3)c3cc(-c4ccc(-c5nc6sc(-c7cccs7)nc6s5)s4)sc32)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c(OC)c(-c2ccc(-c3ccc4c(c3)[Si](C)(C)c3ccccc3-4)s2)c2nsnc2c1-c1cccs1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc[se]c1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)c3nsnc32)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)CC(C=Cc2ccc(N(c3ccc(-n4c5ccccc5c5ccccc54)cc3)c3ccc(-n4c5ccccc5c5ccccc54)cc3)cc2)=CC(=C(C#N)C(=O)O)C1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2ccccc2-c2ccc(N(c3ccc4cc(C=Cc5ccc(C=C(C#N)C(=O)O)s5)oc4c3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CN1C(=O)C2=C(c3ccc(-c4ccco4)o3)N(C)C(=O)C2=C1c1ccco1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1c2cc(-c3ccc(-c4ccc(-c5cccs5)c5nn(C)nc54)s3)sc2c(C)c2ccsc21\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2cc(C=C(C#N)C#N)sc2c2sc(C=C(C#N)C#N)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2cc(-c3cc(C=Cc4sc(-c5ccc(-c6cc(C)cs6)c6nsnc65)cc4C)cs3)sc2c(OC)c2ccsc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C(=Cc1ccc(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)c2nsnc21)c1ccc(N(c2ccccc2)c2ccccc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4cnc(-c5cccs5)c5nsnc54)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1c2ccsc2c(OC)c2cc(-c3sc(-c4sc(-c5cc(C)cs5)c5c4C(=O)N(C)C5=O)cc3C)sc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)c2cc(-c3ccc(-c4ccc(-c5ccc(-c6ccc(C=C(C#N)C#N)s6)s5)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1nc2sc(-c3sc(-c4cc(C)c(-c5nc6sc(-c7sccc7C)nc6s5)s4)cc3C)nc2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc(C=Cc2ccc(C=Cc3cc(C)c(C=Cc4ccc(C=Cc5cc(C)c(C=Cc6ccc(C=Cc7cc(C)c(C=O)cc7C)s6)cc5C)s4)cc3C)s2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc2c3cc(C)sc3c3nc4c(cccc4-c4ccc(-c5ccc6c(c5)C(C)(C)c5cc(-c7cccs7)ccc5-6)s4)nc3c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(C)c4ccsc4c5C)s3)c3nsnc32)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2csc(-c3ccc(-c4ccc(-c5sc(-c6ccc(-c7sccc7C)s6)cc5C)s4)s3)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1nc(-c2nc(C)c(-c3ccc(-c4ccc(-c5ccc(N(c6ccccc6)c6ccccc6)cc5)s4)s3)s2)sc1-c1ccc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" CC1(C)CC(C=Cc2ccc(N(c3ccccc3)c3ccc(N(c4ccccc4)c4ccccc4)cc3)cc2)=CC(=C(C#N)C(=O)O)C1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1c2ccsc2c2sc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc2c1C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=4 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si]1(C)c2cc(-c3cnc(-c4cc5ccccc5s4)c4nsnc43)sc2-c2sc(-c3cnc(-c4cc5ccccc5s4)c4nsnc43)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1csc(C2=NC3SC(c4cc(C)c(-c5cc6c(s5)-c5sccc5[Si]6(C)C)s4)=NC3S2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=3 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cccc(C2N=c3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)s4)c3=NC2c2cccc(OC)c2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cccc(-c2nc3cccc(-c4cccs4)c3nc2-c2cccc(OC)c2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" N#CC(=Cc1ccc(-c2ccc(-c3cc(-c4ccc(-c5ccc(N(c6ccccc6)c6ccccc6)cc5)s4)c(-c4ccc(-c5ccc(N(c6ccccc6)c6ccccc6)cc5)s4)s3)s2)s1)C(=O)O\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1cccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5cc6c(s5)c(OC)c5ccsc5c6OC)s4)c3nc2-c2cccc(OC)c2)c1\\n\"}, {\"instruction\": \"Design a donor with acceptor C60, PCE=5 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1c(C)c(-c2ccc(C3=S=C(c4ccc(C=C(C#N)C#N)s4)C(C)=C3C)s2)sc1-c1ccc(C=C(C#N)C#N)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(C5=C(c6ccccc6)C(c6ccccc6)=C(c6ccc(-c7cccs7)s6)[Si]5(C)C)s4)s3)cc21\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)N1C(=O)C2=C(c3ccc(-c4ccc(C5=S=C(C)C=C5)s4)s3)N(C(=O)OC)C(=O)C2=C1c1ccc(-c2ccc(-c3ccc(C)s3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COC(=O)c1cc2c(-c3cccs3)sc(-c3ccc(-c4cc5c(s4)c(-c4cc(F)c(C)s4)c4ccsc4c5-c4cc(F)c(C)s4)s3)c2s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" COc1ccc2c(c1)-c1cc(OC)c(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc1[Si]2(C)C\\n\"}, {\"instruction\": \"Design a donor with acceptor PC71BM, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cncc5nc6c7ccsc7c7sccc7c6nc53)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1\\n\"}, {\"instruction\": \"Design a donor with acceptor TiO2, PCE=2 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1cc(C=C(C#N)C(=O)O)sc1-c1cc(C)c(-c2cc(C)c(-c3ccc(N(c4ccc5c(c4)C(C)(C)c4ccccc4-5)c4ccc5c(c4)C(C)(C)c4ccccc4-5)cc3)s2)s1\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=1 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" Cc1ccsc1-c1sc(-c2sc(C3=S=C(c4sccc4C)C(C)=C3)cc2C)c2nc3c(nc21)-c1cccc2cccc-3c12\\n\"}, {\"instruction\": \"Design a donor with acceptor PC61BM, PCE=0 for a organic solar cell### ->\", \"input\": \"\", \"output\": \" C[Si]1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(C5=C(c6ccccc6)C(c6ccccc6)=C(c6ccc(-c7cccs7)s6)[Si]5(C)C)s4)s3)cc21\\n\"}]"
  },
  {
    "path": "dataset/opv/opv_regression_test.json",
    "content": "[{\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1sc2csc(-c3sc4c(c3F)c(OC)c3scc(F)c3c4OC)c2c1F, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.9647829909344999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3cc(C)c(-c4cc5cc6sc(-c7sc(-c8sc(-c9sc(C=C(C#N)C(=O)OC)cc9C)cc8C)cc7C)cc6cc5s4)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.1867204122020003\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(-c3cc4c5cccc6c7cccc8c9cc(-c%10ccc%11c(c%10)C(C)(C)c%10ccccc%10-%11)cc%10c%11cccc%12c%13cccc%14c(c3)c4c3c(c65)c(c78)c(c9%10)c(c%12%11)c3c%13%14)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.278765206869375\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4ccc5ccccc5c4)s3)N(C)C(=O)C2=C1c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.8737091924184612\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc4cc(C=Cc5ccc(C=C(C#N)C(=O)O)s5)sc4c3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 3.0767988595741183\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c(OC)c(-c2ccc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)s2)c2nsnc2c1-c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.6521542521282357\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5cc6c(s5)c(-c5ccc(C)s5)c5ccsc5c6-c5ccc(C)s5)s4)c3nc2-c2cccc(OC)c2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.2918886763694737\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3ccc(-c4c5nonc5c(-c5cccs5)c(OC)c4OC)s3)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.1547619483564704\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si]1(C)c2ccsc2-c2sc(-c3cccc4nsnc43)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5002880322\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4cc5ccccc5c5ccccc45)s3)N(C)C(=O)C2=C1c1ccc(-c2cc3ccccc3c3ccccc23)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.769331083826875\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2csc(-c3cc(-c4ccc(C)s4)c(-c4ccc(C5=C6C(=O)N(C)C(c7cccs7)=C6C(=O)N5C)s4)s3)c2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.6747588890825003\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2ccc(-c3c4cc(-c5cc(C)c(-c6ccc(-c7sc(C=C8SC(=S)N(C)C8=O)cc7C)s6)s5)sc4c(-c4ccc(-c5ccc(C)s5)s4)c4cc(-c5cc(C)c(-c6ccc(-c7sc(C=C8SC(=S)N(C)C8=O)cc7C)s6)s5)sc43)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.5846847955966665\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(C=C2C(=O)c3ccccc3C2=O)sc1-c1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(C6=S=C(C=C7C(=O)c8ccccc8C7=O)C=C6C)cc5C)cc4C)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.8773311004084996\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5c4=NC(c4ccccc4)C(c4ccccc4)N=5)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.2720709585199996\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc3c(c2)C(C)(C)c2c-3c3c(c4c2-c2ccc(N(c5ccc(OC)cc5)c5ccc(OC)cc5)cc2C4(C)C)-c2ccc(-c4ccc(C=C(C#N)C(=O)O)s4)cc2C3(C)C)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.427153803663333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : c1csc(-c2cc(-c3cccs3)c(-c3cccs3)s2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.13399535021683331\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1sc(-c2sc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc2C)c2nc3c4ccccc4c4ccccc4c3nc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.11422167613412\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(C(C#N)=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.8469232959940007\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si]1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.1115736763411768\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2ccc(-c3ncc(-c4cc5c(s4)-c4sc(-c6cnc(-c7ccc(-c8ccc(C)s8)s7)c7nsnc76)cc4[Si]5(C)C)c4nsnc43)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.58173364862\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4cnc(-c5cccs5)c5nccnc45)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.034234363908571\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3cc(-c4ccc(-c5sc(-c6cccs6)c6c5C(=O)c5c(C)sc(C)c5C6=O)s4)sc3c(-c3ccc(C)s3)c3ccsc32)s1, and Acceptors: PC71B? ->\", \"input\": \"\", \"output\": \" 1.3557601881549999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3sc(C=C(C#N)C(=O)O)c4c3OCCO4)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.1223570583294733\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(C=C2C(=O)N(C)C(=O)N(C)C2=O)sc1-c1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(C6=S=C(C=C7C(=O)N(C)C(=O)N(C)C7=O)C=C6C)cc5C)cc4C)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.5438690995483335\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1ccc2c3ccccc3n(-c3ccc(OC)cc3)c2c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.60714363031805e-05\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc(-c2nc(C)c(-c3ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s3)s2)sc1-c1cccs1, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 0.9934345167667693\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2cc(-c3cc4c(s3)-c3sc(C=C(C#N)C(=O)O)cc3C4(C)C)ccc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.7580897776333124\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2c(csc2-c2cc3c(s2)c(OC)c2ccsc2c3OC)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.816697207225\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(C3c4ccccc4-c4ccc(-c5ccc(-c6c7nsnc7c(-c7cccs7)c7nc(-c8ccccc8)c(-c8ccccc8)nc76)s5)cc43)cc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.9584033399099994\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2sc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc2cc2c1cc1cc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)sc1c2OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.5712028954006247\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4cnc(-c5cccs5)c5nonc54)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.660110176036876\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4cc5c(s4)-c4sc(-c6cc(C)c(-c7ccc(C8=S=C(C=C(C#N)C(=O)OC)C=C8C)s7)s6)cc4[Si]5(C)C)cc3C)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.99883929396\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5cccs5)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.37253640233033336\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(C#N)=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=C(C#N)C#N)s4)cc3)c3ccc(-c4ccc(C=C(C#N)C#N)s4)cc3)cc2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 4.16626298147\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(-c2ccc(-c3cc(C)c(-c4cccs4)s3)c3nsnc32)sc1-c1cccs1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.1085430600543744\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CSc1ccc(-c2ccc(-c3csc(-c4cc(-c5ccc(-c6ccc(SC)s6)s5)sc4-c4sc(-c5ccc(-c6ccc(SC)s6)s5)cc4-c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)c3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.8006861176614546\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3cc(C)c(-c4nc5sc(-c6sccc6C)nc5s4)s3)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1875105938582358\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1sccc1C(=O)OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.6089602587020866e-09\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3sc(-c4ccc(-c5cc(C)cs5)c5nsnc54)cc3C)sc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.1423649905118753\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1sc2c(-c3ccc(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)s3)sc(-c3cccs3)c2c1F, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.4495046858544445\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(-c2cc(-c3ccc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)c(-c3ccc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)s2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.5973998378745002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2sc(-c3ccc(-c4cc(C)c(-c5cc(C)c(-c6ccc7c8cc9c(cc8n(C)c7c6)c6ccccc6n9C)s5)s4)c4nsnc43)cc2C)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.4983938473687504\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1ccc(-c2sc(-c3nc(C)c(-c4ccc(C5=S=C(c6cc7c(s6)-c6sccc6[Si]7(C)C)C=C5C)s4)s3)nc2C)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.8841503618083574\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2nc3cccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5cc(-c7cccs7)ccc5-6)s4)c3nc2-c2ccc(C)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.7802330196269374\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(C#N)=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)cc2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.145799248773889\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4ccc(C(F)(F)F)cc4)s3)N(C)C(=O)C2=C1c1ccc(-c2ccc(C(F)(F)F)cc2)s1, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 3.8597814580363634\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2nc3sc(-c4cc(C)c(-c5cc6c(s5)-c5sccc5[Si]6(C)C)s4)nc3s2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.0298555764427497\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(C5=C(c6ccccc6)C(c6ccccc6)=C(c6ccc(-c7cccs7)s6)[Si]5(C)C)s4)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.5807495198364665\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2c1=S=C(c1cc(C)c(-c3sc(-c4nc(C)c(-c5sccc5C)s4)nc3C)s1)C=2, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.8394545820709475\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)s4)c3nc2-c2ccc(OC)cc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.8635532341087498\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC(=O)c1cc2csc(-c3cc4c(s3)c(-c3ccc(C)s3)c3ccsc3c4-c3ccc(C)s3)c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.7369657743917333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC(=O)c1cc2c(csc2-c2cc3c(s2)c2sccc2c(C)c3C)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.85711710928375\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c(OC)c(-c2cc3sc(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)cc3s2)c2nsnc2c1-c1cc2sccc2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.9449274082894448\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1csc2c1C(C)(C)c1cc(-c3scc4c3C(=O)N(C)C4=O)sc1-2, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.621752851868\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4ccccc4)s3)N(C)C(=O)C2=C1c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.7823712876408333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(-c3ccc(N(c4ccccc4)c4ccc(C=Cc5ccc(C=C(C#N)C#N)s5)cc4)cc3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.2443164688457142\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1ccc(-c2sc(-c3ccc4c(c3)N(C)C(=O)C4=C3c4ccccc4N(C)C3=O)cc2C)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.684988043103334\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccsc2-c2sc(-c3cccc4nsnc43)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.53784351879\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(C#Cc2ccc(C#Cc3ccc(-c4ccc(-c5ccc(C#Cc6ccc(C#Cc7ccc(OC)c(OC)c7)cc6)s5)c5nsnc54)s3)cc2)cc1OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.019056214706842\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4cccs4)s3)N(C)C(=O)C2=C1c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.8050552545041665\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(-c4ccc(C=C(C#N)C#N)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.77113310156\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4cccs4)o3)N(C)C(=O)C2=C1c1ccco1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5042745456400002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(C=C(c2ccc(N(c3ccccc3)c3ccccc3)cc2)c2ccc(N(c3ccccc3)c3ccccc3)cc2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.107742366591765\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2c1=S=C(c1ccc(-c3sc(-c4nc(C)c(-c5cccs5)s4)nc3C)s1)C=2, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.2425964950846156\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(C=Cc3ccc(C=C(C#N)C(=O)O)s3)cc2)c2ccc(OC)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.9615722362849997\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1ccc(N(c2ccccc2)c2ccc(C=C3SC(=S)N(CC(=O)O)C3=O)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.178500423377\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(-c2c3cc(-c4cccs4)sc3c(-c3cc(C)c(C)s3)c3cc(-c4ccc(-c5ccc6c(c5F)N(C)C(=O)C6=C5c6cccc(F)c6N(C)C5=O)s4)sc32)sc1C, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 3.7733310742712503\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c4sccc4c4cc(C)c(C)cc54)s3)c3nsnc32)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.07479399034375\\n\"}]"
  },
  {
    "path": "dataset/opv/opv_regression_train.json",
    "content": "[{\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2csc(-c3cccs3)c2s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.2955029771955\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccsc1-c1sc(-c2scc3c2C(=O)N(C)C3=O)cc1OC, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.6507196035779375\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3cc(C)c(-c4sc(-c5sccc5C)c5c4C(=O)N(C)C5=O)s3)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.8823683564068826\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COCc1cc2csc(-c3cc4c(s3)c(OC)c3ccsc3c4OC)c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.21331263283306665\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5ccc(C6=C(c7ccccc7)C(c7ccccc7)=C(c7ccc(-c8ccc(C9=S=CC=C9)s8)s7)[Si]6(C)C)s5)s4)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.3136011530287647\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2csc(-c3cc4c(s3)c(C)c3ccsc3c4C)c2s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.5541103553132857\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1sc2c(-c3ccc(-c4cc5c(s4)c(-c4ccc(OC)cc4)c4ccsc4c5-c4ccc(OC)cc4)s3)sc(-c3cccs3)c2c1F, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.328477827452222\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(C=Cc4ccc(C(F)(F)F)cc4)s3)N(C)C(=O)C2=C1c1ccc(C=Cc2ccc(C(F)(F)F)cc2)s1, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 3.950155704261764\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1C1=NC2SC(c3sc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)cc3C)=NC2S1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.5710456452453749\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2csc(-c3ccc(-c4ccc(-c5sccc5C)s4)s3)c2s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.7142583502116362\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccsc2-c2sc(-c3c4nsnc4cc(F)c3F)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.0060899066099998\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1sc2c(-c3ccc(-c4cc5c(s4)c(-c4cc(F)c(C)s4)c4ccsc4c5-c4cc(F)c(C)s4)s3)sc(-c3cccs3)c2c1F, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.7280969436994116\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3cc4sc(-c5cccs5)cc4s3)N(C)C(=O)C2=C1c1cc2sccc2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.9670029455469231\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(C=CC=C(C#N)C(=O)O)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.682388852454118\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : O=C1c2ccccc2C(=O)C1=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)cc2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.9234025336072225\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C#Cc1cc2c(s1)-c1sc(C#Cc3scc4nc(-c5ccccc5)c(-c5ccccc5)nc34)cc1C2(C)C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.90131535906\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3sc4cc(-c5scc6cc(S(C)(=O)=O)sc65)sc4c3c(-c3ccc(C)s3)c3sc4ccsc4c32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.6731741806688002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2ccc(C3=C4C(=O)N(C)C(c5ccc(-c6cc(C)cs6)s5)=C4C(=O)N3C)s2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5723396099987499\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2ccc(-c4nnc(-c5cccs5)nn4)s2)cc1C3(C)C, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.58064173323\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c(OC)c(-c2ccc(-c3cc4c(s3)c(-c3ccc(C)s3)c3ccsc3c4C3=S=C(C)C=C3)s2)c2nsnc2c1-c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.7729826235586665\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1ccc2c3ccc(C=Cc4sc(-c5ccc(-c6ccc(-c7cc(C)cs7)s6)s5)cc4C)cc3n(-c3ccc(OC)cc3)c2c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.5539810246536112\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nccnc45)s3)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.297329158795\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cc(OC)cc(-c2nc3c(nc2-c2cc(OC)cc(OC)c2)c(-c2cccs2)sc3-c2cccs2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.4415794567042859\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3cc(-c4sc5cc(-c6ccc(-c7csc8c(C)csc78)c7nsnc76)sc5c4C)sc3c(-c3ccc(C)s3)c3ccsc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.1338107065246663\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2cccc4nsnc42)cc1C3(C)C, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5700343680100002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CSc1ccc(-c2ccc(-c3ccc([Si](c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)(c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)c4ccc(-c5ccc(-c6ccc(SC)s6)s5)s4)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.4687897398576498\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2csc(-c3cc4c(s3)c(OC)c3ccsc3c4OC)c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.552601922856357\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2cc3c4nsnc4c(-c4cc(C)c(-c5cc6c(s5)c(-c5cc(C)c(C)s5)c5ccsc5c6C5=S=C(C)C(C)=C5)s4)cc3c3nsnc32)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.9087616109170584\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1cc(C#N)c(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1C#N)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 5.037032134375333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(-c5ccc(C=C(C#N)C(=O)O)s5)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.560824158846429\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(N(c2ccccc2)c2ccccc2)cc1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 0.612476318473\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2sccc2c2cc(-c3cc(C)c(-c4nc5sc(-c6sccc6C)nc5s4)s3)sc2c1OC, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.0569752673118824\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(C=C(C#N)C(=O)O)sc1-c1cc(C)c(-c2cc(C)c(-c3cc4ccc(N(c5ccc6c(c5)C(C)(C)c5ccccc5-6)c5ccc6c(c5)C(C)(C)c5ccccc5-6)cc4s3)s2)s1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.3688369146589996\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.100690670119334\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2csc(-c3cc4c(s3)c(-c3ccc(C)s3)c3ccsc3c4-c3ccc(C)s3)c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.5917605359245715\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3cc4c(s3)-c3sc(C=C(C#N)C(=O)O)cc3C4(C)C)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.6867661221173331\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(-c2nc3c(nc2-c2ccc(OC)cc2)c(-c2ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s2)sc3-c2cccs2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.9993568492045621\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C(=Cc1cccc2nsnc21)c1ccc(N(c2ccc(C=Cc3cccc4nsnc43)cc2)c2ccc(C=Cc3cccc4nsnc43)cc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.8254955452799997\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1ccc(-c2ccc(-c3sccc3C)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.3198192472321538\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=CC=Cc1ccc(N(c2ccccc2)c2ccccc2)cc1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.2774454648153843\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.312709405978461\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2nnc(-c3cc(C)c(-c4cc5c(s4)-c4sccc4[Si]5(C)C)s3)nn2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.3620578975333335\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : c1csc(-c2ccsc2-c2cccs2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.00201509655741\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(C=C(C#N)c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 3.7029430427306673\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3cc(-c4ccc(-c5sc(-c6cccs6)c6cc(S(C)(=O)=O)sc65)s4)sc3c(-c3ccc(C)s3)c3ccsc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5454113197055557\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)CC(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)=CC(=C(C#N)C(=O)O)C1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.935123093346428\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3ccc(-c4ccc(C=C(C#N)C(=O)O)s4)s3)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.1675291630876474\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC(=O)c1sc2csc(-c3cc4c(s3)c(C)c3ccsc3c4C)c2c1F, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1745651833525002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(-c2nc3c(-c4scc5c4OCCO5)ccc(-c4sc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)c5c4OCCO5)c3nc2-c2ccc(OC)cc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.4061928157267\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1ccc2c3ccc(C=Cc4cccs4)cc3n(-c3ccc(OC)cc3)c2c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.22241767952837502\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccsc1-c1ccc(-c2sc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc2OC)c2nsnc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.8480353941962144\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c(OC)c(-c2ccc(-c3ccc4c5ccccc5n(C)c4c3)s2)c2nsnc2c1-c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5961405108987499\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2sc(-c3cc(C)c(-c4cccs4)s3)c3sc(C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc23)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1531829079066664\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1nc2sc(-c3sc(-c4ccc5c6ccccc6n(C)c5c4)cc3C)nc2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.7674782479114999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2c3nsnc3c(-c3cc(C)c(-c4cc5c(s4)c(C)c4ccsc4c5C)s3)c(F)c2F)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.6785772030646657\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1c2ccsc2c(C)c2cc(-c3ccc(-c4cnc(-c5cccs5)c5nsnc54)s3)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.604466261764668\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC(=O)c1cc2c(csc2-c2cc3c(s2)c(C)c2ccsc2c3C)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.0970314967966666\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1cc(OC)c(C=Cc2cc(C=C(C#N)c3ccc([N+](=O)[O-])cc3)ccc2C=C(C#N)c2ccc([N+](=O)[O-])cc2)cc1OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 5.7216311600204985\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc2c3cc(C)sc3c3nc4c(-c5ccc(-c6ccc7c8ccccc8n(C)c7c6)s5)ccc(-c5cccs5)c4nc3c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.667487626229231\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2cc3c(cc21)-c1cc2c(cc1C3(C)C)-c1ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc1C2(C)C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.0871277931719994\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2ccc(-c4ccc(-c5cccs5)c5nsnc54)s2)cc1C3(C)C, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.72766876557\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-n2c(-c3ccsc3)nc3c2c2ccc(C)cc2c2cc(C)ccc32)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.004334139435375\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1sc2c(csc2-c2cc3c(s2)c(OC)c2ccsc2c3OC)c1F, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.6365631533970001\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2c1=S=C(c1cc(C)c(-c3ccc(-c4sc(-c5nc(C)c(-c6ccc(-c7sccc7C)s6)s5)nc4C)s3)s1)C=2, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.1657953481672223\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1=CC(c2ccc(-c3cc(C)c(-c4cc5c(s4)c4sccc4c4nc(C)c(C)nc54)s3)c3nsnc32)=S=C1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.2166346499457146\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2cc3c4nsnc4c(-c4cc(C)cs4)cc3c3nsnc32)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.8190675148375\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3scc4sc(S(C)(=O)=O)cc43)sc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.7755386769242222\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc(N(c2ccccc2)c2ccccc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.8015776939015384\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2nc3c(nc2-c2ccc(C)cc2)c(-c2ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s2)sc3-c2cccs2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.3042464905446152\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(C=Cc3cc4c(s3)-c3sc(C=C(C#N)C(=O)O)cc3C4(C)C)cc2)c2ccc(OC)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.7237374420791671\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cccc5nc6c7ccsc7c7sccc7c6nc53)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.3553068398342858\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccsc2c2sc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.2127021276440002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c(OC)c(-c2ccc(-c3ccc(-c4ccc5c6ccccc6n(C)c5c4)s3)s2)c2nsnc2c1-c1ccc(-c2cccs2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5656692685480005\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)s4)c3nc2-c2cccc(OC)c2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1366022269916667\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3ccc4ccc5cccc6ccc3c4c56)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.2575067334322223\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(C=C(C#N)C#N)sc2-c2sc(C=C(C#N)C#N)cc21, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 0.0\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(C=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.883900262544\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(-c2c3ccsc3c(-c3cc(C)c(C)s3)c3cc(-c4ccc5c(c4)N(C)C(=O)C5=C4c5ccccc5N(C)C4=O)sc32)sc1C, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.734425328\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc2c(c1)C(C)(C)c1cc(N(c3ccccc3)c3cccc4ccccc43)ccc1-2, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.809821609\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(C(C#N)=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 3.9691414412637505\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc2c(c1)c1cc(N(c3ccccc3)c3ccccc3)ccc1n2C, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.671517483070625\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.0518776135999994\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(-c4ccc(C)cc4)c4ccsc4c5-c4ccc(C)cc4)s3)c3nsnc32)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.0143618777519996\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C#Cc1cc(OC)c(C#Cc2scc3nc(-c4ccccc4)c(-c4ccccc4)nc32)cc1OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.5896403356783333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C#Cc1cc2c(s1)c1sc(C#Cc3cccc4nsnc43)cc1n2C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.835245723608\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4nnc(-c5cccs5)c5nonc54)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 4.8986056661984625\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5ccc(-c6cccs6)c6nsnc65)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.7231475878868756\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(-c2cc(C)c(C3=S=CC=C3)s2)sc1-c1ccc(-c2cccc3nsnc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.7495300331458823\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c(-c2ccc(C=C(C#N)C(=O)O)cc2)ccc1-c1ccc(N(c2ccccc2)c2ccccc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.725716055865333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : c1csc(-c2ccc(-c3ccc(-c4c(-c5ccc(-c6cccs6)s5)sc(-c5ccc(-c6cccs6)s5)c4-c4ccc(-c5ccc(-c6cccs6)s5)s4)s3)s2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.7010837417522\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(OCCCCCCOc2ccc(C=C(C#N)c3ccc([N+](=O)[O-])cc3)cc2O)c(O)c1)c1ccc([N+](=O)[O-])cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 0.7477032074923572\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(C#Cc4cc5ccccc5c5ccccc45)s3)N(C)C(=O)C2=C1c1ccc(C#Cc2cc3ccccc3c3ccccc23)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.829864018905263\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4cc5sc(C=C(C#N)C(=O)O)cc5s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.310894943336667\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1sc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)c2c1OCCO2)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.3274368877387501\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccsc2-c2sc(-c3ccc(-c4nc5sc(-c6cccs6)nc5s4)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1665500233749997\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(C)sc2c(OC)c2cc(-c3ccc(-c4sc(-c5ccc(C)s5)c5c4C(=O)N(C)C5=O)s3)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.2284834559558824\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)CC(C=Cc2ccc(N(c3ccc(N(c4ccccc4)c4ccccc4)cc3)c3ccc(N(c4ccccc4)c4ccccc4)cc3)cc2)=CC(=C(C#N)C(=O)O)C1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.5967142258433331\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3c4ccccc4cc4ccccc43)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.1554229012564705\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C#Cc1cc2c(s1)c1sc(C#Cc3scc4nc(-c5ccccc5)c(-c5ccccc5)nc34)cc1n2C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.6895063007500002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1c2ccccc2C(=C2c3ccc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)cc3N(C)C2=O)C1=O, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.5507185769959997\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(C=C(C#N)C(=O)O)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.018992051167333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc2c(nc1C)c(-c1ccc(-c3ccc4c5ccccc5n(C)c4c3)s1)sc2-c1cccs1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1019885182055555\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si]1(C)c2cc(-c3cnc(-c4cccs4)c4nsnc43)sc2-c2sc(-c3cnc(-c4cccs4)c4nsnc43)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 3.922806508109999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C(=C1Sc2ccccc2S1)c1ccc(N(c2ccc(C=C3Sc4ccccc4S3)cc2)c2ccc(C=C3Sc4ccccc4S3)cc2)cc1, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" -0.025473488378258823\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2ccc(-c3cc(C)cs3)c3nsnc32)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.7464246492259998\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(C)c(-c2c3cc(-c4ccc(-c5ccc(-c6cccs6)c6nsnc65)s4)sc3c(-c3sc(C)cc3C)c3ccsc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.4019924391288883\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(C)cc(-c2ccc(N(c3ccc(-c4cc5c(s4)-c4sc(C=C(C#N)C(=O)O)cc4C5(C)C)cc3)c3ccc(-c4cc(C)cc(C)c4)cc3)cc2)c1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.060122308256666\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4ccc5c(c4)C(C)(C)c4cc(-c6cc(C)c(-c7ccc(-c8sc(C=C(C#N)C(=O)OC)cc8C)s7)s6)ccc4-5)cc3C)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.8810756640420006\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4nnc(-c5cccs5)c5nccnc45)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.997289598042\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1cc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)c(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.2508351373699993\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2ccc(-c3ccc(-c4ccc(N(c5ccc(-c6ccc(-c7ccc(-c8ccc(C)s8)s7)s6)cc5)c5ccc(-c6ccc(-c7ccc(-c8ccc(C)s8)s7)s6)cc5)cc4)s3)s2)s1, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 0.28328885227085715\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2sc(-c3nc4cc5sc(-c6cc(C)c(-c7cc(C)cs7)s6)nc5cc4s3)cc2C)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.89090034744775\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2cc3c(cc21)-c1ccc(-c2ccc(-c4ccc(-c5cccs5)c5nsnc54)s2)cc1C3(C)C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.1131244173699995\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COCc1sc2c(csc2-c2cc3c(s2)c(OC)c2ccsc2c3OC)c1F, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.2713881963007779\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C#Cc1sc(C#Cc2scc3nc(-c4ccccc4)c(-c4ccccc4)nc23)c(C)c1C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.7091483083237498\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5ccc(C6=C7C(=O)N(C)C(c8cccs8)=C7C(=O)N6C)s5)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.2937429658215789\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc(-c2ccc3c(c2)C(C)(C)c2cc(N(c4ccccc4)c4ccccc4)ccc2-3)s1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.0522110209645\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3sc(C4=S=Cc5ccccc54)c4ccccc43)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.8182908123623158\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c7ccccc7n(C)c6c5)s4)c3nc2-c2ccc(OC)cc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.8310985287308751\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)Oc2cc(-c3c4nsnc4cc(F)c3F)sc2-c2sccc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.2470169671533333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)sc1-c1nc2sc(-c3sc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)cc3C)nc2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.6885637157548824\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccc(-c5ccc(C=CC=C(C#N)C(=O)O)s5)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.7913456822800002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1ccc(N(c2ccccc2)c2ccc(-c3ccc(C=C4SC(=S)N(CC(=O)O)C4=O)s3)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.124051089384\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(-c2ccc(-c3ccc(C=C(C#N)c4ccc([N+](=O)[O-])cc4)s3)c3c2C(=O)OC3=O)s1)c1ccc([N+](=O)[O-])cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 4.149924975062104\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)s3)c3nsnc32)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.0622247677077774\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si]1(C)c2ccsc2-c2sc(-c3nc4sc(-c5cc6c(s5)-c5sc(-c7cc8sccc8s7)cc5[Si]6(C)C)nc4s3)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.1558353278216669\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(C=C(C#N)C(=O)OC)cc5C)cc4C)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.830544170175882\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(-c4ccc(C=C(C#N)C(=O)O)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3cccc4ccccc43)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.668117775930589\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1=CC(c2cc(C)c(-c3sc(-c4cc(C)c(-c5nc6scnc6s5)s4)cc3C)s2)=S=C1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.9772231652101334\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1nc2sc(-c3sc(-c4cc5c(s4)c(C#C[Si](C)(C)C)c4ccsc4c5C#C[Si](C)(C)C)cc3C)nc2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.533645669216111\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(C=Cc3sc(C=C(C#N)C(=O)O)c4c3OCCO4)cc2)c2ccc(OC)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.2987128104405883\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1cc(OC)ccc1OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.4652725567166326e-15\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3scc4c3C(=O)N(C)C4=O)sc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.8683759932687144\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(C(=Cc3ccc(C=C(C#N)C(=O)O)s3)c3ccc(N(c4ccc(OC)cc4)c4ccc(OC)cc4)cc3)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.3380343881465004\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3ccsc3c(-c3ccc(C)s3)c3cc(-c4ccc(C5=C6C(=O)N(C)C(c7cccs7)=C6C(=O)N5C)s4)sc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.9901078349441665\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(C=Cc2ccc(C=Cc3cc(OC)c(C=Cc4ccc(C=Cc5cc(OC)c(C=Cc6ccc(C=Cc7cc(OC)c(C=O)cc7OC)s6)cc5OC)s4)cc3OC)s2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.2354299750280375\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(-c3ccc(C4=C(c5ccccc5)C(c5ccccc5)=C(c5cccs5)[Si]4(C)C)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.6290121356384\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc(-c2nc(C)c(-c3ccc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)s3)s2)sc1-c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.0511473487585714\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)sc1-c1cnc(-c2ncc(-c3sc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)cc3C)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.7357676070440001\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(C#Cc2ccc(-c3ccc(-c4ccc(C#Cc5ccc(OC)c(OC)c5)s4)c4nsnc43)s2)cc1OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.565002195222001\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccsc2c2sc(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.6443011241788237\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc(-c2nc(C)c(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)sc1-c1ccc(N(c2ccccc2)c2ccccc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.38765386118764283\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3cc(-c4cc5sc(C6=C7C(=O)N(C)C(c8cc9sccc9s8)=C7C(=O)N6C)cc5s4)sc3c(-c3ccc(C)s3)c3ccsc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.95552728619\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4sc(-c5cccs5)c5nc(-c6ccccc6)c(-c6ccccc6)nc54)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.5042011241500002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2c(csc2-c2sc3c(c2F)c(OC)c2scc(F)c2c3OC)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.9303209186841249\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4cc5c(s4)-c4sccc4[Si]5(C)C)s3)N(C)C(=O)C2=C1c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.4828183529\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3sc(-c4scc5c4C4C=CC5CC4(C)C)c4c3C3C=CC4C(C)(C)C3)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.173870587061\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(C=C2C(=O)c3ccccc3C2=O)sc1-c1cc(C)c(-c2ccc(-c3sc(C4=S=C(C=C5C(=O)c6ccccc6C5=O)C=C4C)cc3C)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.626123806380589\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1cc(OC)c(C=Cc2ccc(N(c3ccccc3)c3ccc(C=C(C#N)c4ccc([N+](=O)[O-])cc4)cc3)cc2)cc1OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.362453544114737\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)c2csc(-c3cc4c(s3)-c3sccc3[Si]4(C)C)c2C1=O, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.6313223685730001\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1=CC(c2cc(C)c(-c3ccc(-c4sc(-c5nc(C)c(-c6cccs6)s5)nc4C)s3)s2)=S=C1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.050189225\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2c1c1c(c3c2C(C)(C)c2cc(N(c4ccccc4)c4ccccc4)ccc2-3)C(C)(C)c2cc(N(c3ccccc3)c3ccccc3)ccc2-1, and Acceptors: Tio2? ->\", \"input\": \"\", \"output\": \" 2.4258510142475003\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3ccsc3c(-c3ccc(C)s3)c3cc(-c4scc5cc(S(C)(=O)=O)sc54)sc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.6112066034965834\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C(=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)cc2)s1)c1cccs1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.40380805528389985\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(C=C(C#N)C(=O)O)s3)ccc2-c2ccc(N(c3ccccc3)c3cccc4ccccc43)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.1901143322887497\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si](C)(C)C#Cc1c2ccccc2c2ccc3c(C#C[Si](C)(C)C)c4ccccc4c4ccc1c2c34, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.672743451855\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1c(-c2cccs2)sc2c(C)c(-c3ccc(-c4scc5c4C(=O)N(C)C5=O)s3)sc12, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.1993347740155715\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2ccc(-c3cc(F)c(-c4cc5c(s4)-c4sc(-c6c7nsnc7c(-c7ccc(-c8ccc(C)s8)s7)cc6F)cc4[Si]5(C)C)c4nsnc43)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.7527525622471425\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3scc4sc(C(C)=O)cc43)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.0878760815993336\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccccc21, and Acceptors: PDI? ->\", \"input\": \"\", \"output\": \" 0.0\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5cc6c7c8c(cccc8CCc7c5)n6C)s4)c3nc2-c2ccc(OC)cc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.7457477457499232\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3scc4sc(C(C)=O)c(F)c43)sc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.2084016944842855\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(-c2cc3c4nsnc4c(-c4cc(C)c(-c5cccs5)s4)cc3c3nsnc32)sc1-c1cccs1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.2409350104233337\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1c2ccccc2C(=C2c3ccc(-c4cccs4)cc3N(C)C2=O)C1=O, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.6974192257937504\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(C#Cc2c3ccccc3c(C#Cc3ccc(OC)c(OC)c3)c3ccccc23)cc1OC, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1842195568971425\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1c2cc(-c3ccc(-c4c5nn(C)nc5c(-c5cccs5)c(F)c4F)s3)sc2c(C)c2ccsc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1518803585800002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2cc(-c3ccc(C)s3)c(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)s2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.5755403434600004\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2cccc(-n3c4ccccc4c4ccc(-c5ccc(-c6c7nsnc7c(-c7cccs7)c7nc(-c8ccccc8)c(-c8ccccc8)nc76)s5)cc43)c2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.1069939761525007\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3cc4sccc4s3)N(C)C(=O)C2=C1c1cc2sccc2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.9494909476666666\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(-c3cc(C)c(-c4ccc(-c5sc(C=C6SC(=S)N(C)C6=O)cc5C)s4)s3)sc2c(OC)c2cc(-c3cc(C)c(-c4ccc(-c5sc(C=C6SC(=S)N(C)C6=O)cc5C)s4)s3)sc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.48884347545\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3ccc(-c4sc(-c5cccs5)c5c4C(=O)N(C)C5=O)s3)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.4598779019199997\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc2cc3c(C#C[Si](C)(C)C)c4cc5sc(C)cc5cc4c(C#C[Si](C)(C)C)c3cc2s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.9900627163849999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccsc2-c2cc3c(cc21)-c1sc(-c2ccc(-c4nc5sc(-c6cccs6)nc5s4)s2)cc1C3(C)C, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.1528924305169233\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4cc5c(s4)-c4sccc4C5(C)C)s3)N(C)C(=O)C2=C1c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.385131066686923\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)s3)N(C)C(=O)C2=C1c1cccs1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.727597758828\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2sccc2c2cc(-c3ccc(-c4sc(-c5nc(C)c(-c6cccs6)s5)nc4C)s3)sc2c1OC, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.2004572975299999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc2c(-c3cccs3)nnc(-c3ccc(-c4ccc5c6ccccc6n(C)c5c4)s3)c2nc1C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.9561154469826667\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2cc3c(cc21)-c1ccc(-c2ccc(-c4ccc(-c5cccs5)c5c4=NC(c4ccccc4)C(c4ccccc4)N=5)s2)cc1C3(C)C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.217251005106251\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(C=Cc2ccc(C=Cc3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.98635002599375\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3ccc(C=C(C#N)C(=O)O)s3)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.7095071196461535\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c(-c2ccc(-c3cccc4nsnc43)s2)ccc1C1=S=CC=C1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.5573301164113333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(-c3cc4c(s3)-c3sc(C5=NC6SC(c7cc8c(s7)-c7sccc7[Si]8(C)C)=NC6S5)cc3[Si]4(C)C)sc2c(OC)c2ccsc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.889264936260706\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1, and Acceptors: ICBA? ->\", \"input\": \"\", \"output\": \" 0.0\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(-c3cc4c(s3)-c3sc(-c5nc6sc(-c7cc8c(s7)-c7sccc7[Si]8(C)C)nc6s5)cc3[Si]4(C)C)sc2c(OC)c2ccsc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.2002478545228572\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cccs3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.216950206947\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1sc(-c2sc(-c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc2C)c2nc3c(nc21)-c1cccc2cccc-3c12, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.287963179935714\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4ccc5c6ccc(-c7cc(C)c(-c8ccc(-c9sc(C=C(C#N)C(=O)OC)cc9C)s8)s7)cc6n(C)c5c4)cc3C)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.775279828984501\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4cc5sc6cc(C=C(C#N)C(=O)O)sc6c5s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.4758533006387498\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(-c5cccs5)c5nonc54)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.39611449191625\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cccc2c1ccc(-c1ccc(-c3ccc(-c4cccs4)c4nsnc43)s1)c2OC, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.0033552247947055\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc2c3ccsc3c3sc(-c4ccc(-c5cnc(C6=S=CC=C6)c6nsnc65)s4)cc3c2nc1C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.6175804714749997\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1sc(-c2sc(C3=S=C(c4sccc4C)C=C3C)cc2C)c2nc3c4ccccc4c4ccccc4c3nc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.552969499034667\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3cc(C)c(-c4ccc(-c5sc(-c6sc(-c7sc(C=C(C#N)C(=O)OC)cc7C)cc6C)cc5C)s4)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.2044175072309997\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=CC1=S=C(c2cc(C)c(-c3ccc(-c4sc(-c5sc(-c6ccc(-c7cc(C)c(-c8cc(C)c(-c9ccc(-c%10sc(C%11=S=C(C=C(C#N)C(=O)OC)C=C%11C)cc%10C)s9)s8)s7)c7nsnc76)cc5C)cc4C)s3)s2)C(C)=C1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.785174584944286\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1nnc(-c2sc(-c3cc4c(s3)-c3sccc3C4(C)C)cc2C)nn1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.3273265330571427\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c(-c2ccc(C=C(C#N)C(=O)O)s2)ccc1-c1ccc2c(c1)C(C)(C)c1cc(N(c3ccccc3)c3ccccc3)ccc1-2, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.8548506505993332\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2ccc(-c3sc(-c4cc5c(s4)c(OC)c4cc(-c6cc(C)c(-c7ccc(-c8sc(C=C(C#N)C(=O)OC)cc8C)s7)s6)sc4c5OC)cc3C)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.2167469090689993\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(C=C(C#N)C(=O)O)sc2-c2sc(-c3ccc(N(c4ccc(N5c6ccccc6Sc6ccccc65)cc4)c4ccc(N5c6ccccc6Sc6ccccc65)cc4)cc3)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.7161889451805883\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2nnc(-c3cc(C)c(-c4cc5c(s4)-c4sccc4C5(C)C)s3)nn2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.3455373176366667\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc(-c2nc(C)c(-c3ccc(C4=S=C5c6cc7c(cc6C(C)(C)C5=C4)-c4sccc4C7(C)C)s3)s2)sc1-c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.9895534137700664\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3ccc(-c5ccc(-c6ccc(-c7ccc(-c8cccs8)s7)c7nsnc76)s5)s3)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.502489444147222\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3scc4cc(C(C)=O)sc43)sc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.7407422648902943\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3ccc(C=C(C#N)C(=O)O)o3)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.2271984772100004\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cccc5nsnc53)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.50142390907\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc(C=C(C#N)c4ccc(C=C(C#N)C(=O)O)s4)cc3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 3.2427413024650003\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2ccc(-c3cnc(-c4cc5c(s4)-c4sc(-c6ncc(-c7ccc(-c8ccc(C)s8)s7)c7nsnc76)cc4[Si]5(C)C)c4nsnc43)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 3.199950255404117\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1cc(C)c(-c2ccc(-c3cc(C)c(C4=S=C(c5ccc6c7cc8c(cc7n(C)c6c5)c5ccccc5n8C)C(C)=C4)s3)c3nsnc32)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.4879829002452634\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si]1(C)c2ccsc2-c2sc(-c3cccc4nonc43)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.6436799792949999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2c1=S=C(c1sc(-c3sc(-c4nc(C)c(-c5cc(C)cs5)s4)nc3C)cc1C)C=2, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.0984464464286154\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1c2ccccc2Sc2cc(C=Cc3ccsc3-c3cccs3)ccc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.1709249549997692\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cc2c3ccsc3c3sc(-c4sc(-c5ccc(-c6cc(C)cs6)c6nsnc65)cc4C)cc3c2cc1OC, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.1268151007699996\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc(-c2nc(C)c(-c3ccc(-c4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)s2)sc1-c1ccc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.8106737733017368\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cc2c3ccsc3c3sc(-c4cccc5nsnc54)cc3c2cc1OC, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5687767151876468\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4cc5ccccc5o4)s3)N(C)C(=O)C2=C1c1ccc(-c2cc3ccccc3o2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.580472779503125\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1ccc2c3ccc(C=Cc4ccc(-c5ccc(C6=C(C)C(C)=C(c7ccc(-c8cccs8)s7)S6(=O)=O)s5)s4)cc3n(-c3ccc(OC)cc3)c2c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.7230743113525002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C=Cc1ccc2c3ccc(C=Cc4sc(-c5cc(C)cs5)cc4C)cc3n(-c3ccc(OC)cc3)c2c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.3438163250116154\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(C#N)=Cc1ccc(-c2ccc(N(c3ccc(-c4ccc(C=Cc5cccs5)s4)cc3)c3ccc(-c4ccc(C=C(C#N)C#N)s4)cc3)cc2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 4.832748021690715\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc2c3ccsc3c3sc(-c4ccc(-c5cnc(-c6cccs6)c6nsnc65)s4)cc3c2cc1C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.44401605897\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1sc2csc(-c3cc4c(s3)c(OC)c3ccsc3c4OC)c2c1F, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.9462628918395456\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc(-c2nc(C)c(-c3ccc(C4=S=C5c6sccc6C(C)(C)C5=C4)s3)s2)sc1-c1cccs1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.979425366579\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(N(c2ccc(OC)cc2)c2ccc(-c3sc(-c4cc5sc(C=C(C#N)C(=O)O)cc5s4)c4c3OCCO4)cc2)cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.4909125245316668\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccc(C=C(C#N)C#N)cc2c2cc(C=C(C#N)C#N)ccc21, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 0.60647546646575\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c7ccccc7n(C)c6c5)s4)c3nc2-c2ccc(C)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.0168804956095998\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(-c2ccc(-c3ccc(C=C(C#N)c4ccc([N+](=O)[O-])cc4)s3)c3c2C(=O)N(c2ccc(C(=O)O)cc2)C3=O)s1)c1ccc([N+](=O)[O-])cc1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 3.678681271406876\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(-c4cc(C)c(C)s4)c4ccsc4c5-c4cc(C)c(C)s4)s3)c3nsnc32)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.9072929727153334\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2sc(-c3ccc(-c4ccc(N(c5ccc(-c6ccc(-c7sc(-c8ccc(C)s8)c8c7OCCO8)s6)cc5)c5ccc(-c6ccc(-c7sc(-c8ccc(C)s8)c8c7OCCO8)s6)cc5)cc4)s3)c3c2OCCO3)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" -0.28459081567566663\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)sc2c(OC)c2ccsc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.9875283733708333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(-c3cccs3)sc2c(OC)c2cc(-c3ccc(-c4ccc5c(c4)N(C)C(=O)C5=C4c5ccccc5N(C)C4=O)s3)sc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 3.0172094418199995\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)C(C#N)=Cc1cc(C)c(-c2cc(C)c(-c3ccc(-c4sc(-c5sc(-c6cc7c(s6)c(OC)c6cc(-c8cc(C)c(-c9cc(C)c(-c%10ccc(-c%11sc(-c%12sc(C=C(C#N)C(=O)OC)cc%12C)cc%11C)s%10)s9)s8)sc6c7OC)cc5C)cc4C)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.5217457511777774\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2c(-c3cccs3)sc(-c3ccc(-c4cc5c(s4)c(-c4ccc(C)s4)c4ccsc4c5-c4ccc(C)s4)s3)c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.3112486343173333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2ccc(-c3ccc(C4=C5C(=O)N(C)C(c6ccc(-c7ccc(C8=S=C(C)C=C8)s7)s6)=C5C(=O)N4C)s3)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.0836286454822222\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C(=Cc1ccc(N(c2ccccc2)c2ccccc2)cc1)c1ccc(-c2ccc(-c3ccc(C=Cc4ccc(N(c5ccccc5)c5ccccc5)cc4)s3)c3nsnc32)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.9682544099688332\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(-c3cccs3)sc2c(OC)c2ccsc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.1434098487945\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2cc(C)c(-c3scc4c3C(=O)N(C)C4=O)s2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.3887631514465\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3cc(-c4ccc(C5=C6C(=O)N(C)C(c7cccs7)=C6C(=O)N5C)s4)sc3c(-c3ccc(C)cc3)c3ccsc32)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.863712870145334\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(-c4ccc(-c5ccc(C=C(C#N)C#N)s5)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 4.084415762950001\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)c2csc(-c3cc4c(s3)-c3sccc3C4(C)C)c2C1=O, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.618378355864\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(-c2c3ccsc3c(-c3ccc(C)s3)c3cc(-c4ccc(-c5nc6sc(-c7cccs7)nc6s5)s4)sc32)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.3393903664688236\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c(OC)c(-c2ccc(-c3ccc4c(c3)[Si](C)(C)c3ccccc3-4)s2)c2nsnc2c1-c1cccs1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.652566214126667\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc[se]c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.0\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.5571218120224994\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)c3nsnc32)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 4.180876158947856\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)CC(C=Cc2ccc(N(c3ccc(-n4c5ccccc5c5ccccc54)cc3)c3ccc(-n4c5ccccc5c5ccccc54)cc3)cc2)=CC(=C(C#N)C(=O)O)C1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.413719593488333\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2ccccc2-c2ccc(N(c3ccc4cc(C=Cc5ccc(C=C(C#N)C(=O)O)s5)oc4c3)c3ccc4c(c3)C(C)(C)c3ccccc3-4)cc21, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 3.124895209780588\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CN1C(=O)C2=C(c3ccc(-c4ccco4)o3)N(C)C(=O)C2=C1c1ccco1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.3354769376525\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1c2cc(-c3ccc(-c4ccc(-c5cccs5)c5nn(C)nc54)s3)sc2c(C)c2ccsc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.9272759348008888\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2cc(C=C(C#N)C#N)sc2c2sc(C=C(C#N)C#N)cc21, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 4.91705039032\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2cc(-c3cc(C=Cc4sc(-c5ccc(-c6cc(C)cs6)c6nsnc65)cc4C)cs3)sc2c(OC)c2ccsc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.075549570417059\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C(=Cc1ccc(C=Cc2ccc(N(c3ccccc3)c3ccccc3)cc2)c2nsnc21)c1ccc(N(c2ccccc2)c2ccccc2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1110645439540625\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4cnc(-c5cccs5)c5nsnc54)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.1722520320012495\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1c2ccsc2c(OC)c2cc(-c3sc(-c4sc(-c5cc(C)cs5)c5c4C(=O)N(C)C5=O)cc3C)sc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.249371369536154\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)c2cc(-c3ccc(-c4ccc(-c5ccc(-c6ccc(C=C(C#N)C#N)s6)s5)s4)s3)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 4.134974710592501\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1nc2sc(-c3sc(-c4cc(C)c(-c5nc6sc(-c7sccc7C)nc6s5)s4)cc3C)nc2s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.9210813834900002\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc(C=Cc2ccc(C=Cc3cc(C)c(C=Cc4ccc(C=Cc5cc(C)c(C=Cc6ccc(C=Cc7cc(C)c(C=O)cc7C)s6)cc5C)s4)cc3C)s2)cc1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.092663259166\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc2c3cc(C)sc3c3nc4c(cccc4-c4ccc(-c5ccc6c(c5)C(C)(C)c5cc(-c7cccs7)ccc5-6)s4)nc3c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.4647376581529412\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(-c2ccc(-c3cc(C)c(-c4cc5c(s4)c(C)c4ccsc4c5C)s3)c3nsnc32)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.2092340224418745\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2csc(-c3ccc(-c4ccc(-c5sc(-c6ccc(-c7sccc7C)s6)cc5C)s4)s3)c2s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.7010592098388573\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1nc(-c2nc(C)c(-c3ccc(-c4ccc(-c5ccc(N(c6ccccc6)c6ccccc6)cc5)s4)s3)s2)sc1-c1ccc(-c2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.93964346125805\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : CC1(C)CC(C=Cc2ccc(N(c3ccccc3)c3ccc(N(c4ccccc4)c4ccccc4)cc3)cc2)=CC(=C(C#N)C(=O)O)C1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 1.9381505289757897\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1c2ccsc2c2sc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc2c1C, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.9092748932478574\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si]1(C)c2cc(-c3cnc(-c4cc5ccccc5s4)c4nsnc43)sc2-c2sc(-c3cnc(-c4cc5ccccc5s4)c4nsnc43)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 4.732007238487059\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1csc(C2=NC3SC(c4cc(C)c(-c5cc6c(s5)-c5sccc5[Si]6(C)C)s4)=NC3S2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 0.5411544886378749\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cccc(C2N=c3c(-c4cccs4)ccc(-c4ccc(-c5ccc6c(c5)C(C)(C)c5ccccc5-6)s4)c3=NC2c2cccc(OC)c2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 3.375930995481579\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cccc(-c2nc3cccc(-c4cccs4)c3nc2-c2cccc(OC)c2)c1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.24816102075807694\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : N#CC(=Cc1ccc(-c2ccc(-c3cc(-c4ccc(-c5ccc(N(c6ccccc6)c6ccccc6)cc5)s4)c(-c4ccc(-c5ccc(N(c6ccccc6)c6ccccc6)cc5)s4)s3)s2)s1)C(=O)O, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.713745704286\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(C4=C5C(=O)N(C)C(c6cccs6)=C5C(=O)N4C)s3)cc21, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5984631145273334\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1cccc(-c2nc3c(-c4cccs4)ccc(-c4ccc(-c5cc6c(s5)c(OC)c5ccsc5c6OC)s4)c3nc2-c2cccc(OC)c2)c1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.326774003973684\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1c(C)c(-c2ccc(C3=S=C(c4ccc(C=C(C#N)C#N)s4)C(C)=C3C)s2)sc1-c1ccc(C=C(C#N)C#N)s1, and Acceptors: C60? ->\", \"input\": \"\", \"output\": \" 5.14803316199125\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cn1c2ccccc2c2ccc(-c3ccc(-c4ccc(C5=C(c6ccccc6)C(c6ccccc6)=C(c6ccc(-c7cccs7)s6)[Si]5(C)C)s4)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.4845324969367999\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)N1C(=O)C2=C(c3ccc(-c4ccc(C5=S=C(C)C=C5)s4)s3)N(C(=O)OC)C(=O)C2=C1c1ccc(-c2ccc(-c3ccc(C)s3)s2)s1, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 2.1252135838531254\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COC(=O)c1cc2c(-c3cccs3)sc(-c3ccc(-c4cc5c(s4)c(-c4cc(F)c(C)s4)c4ccsc4c5-c4cc(F)c(C)s4)s3)c2s1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 1.5861156094235718\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : COc1ccc2c(c1)-c1cc(OC)c(-c3ccc(-c4ccc(-c5cccs5)c5nsnc54)s3)cc1[Si]2(C)C, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.8871023603069228\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccc(C2(c3ccc(C)cc3)c3ccsc3-c3cc4c(cc32)-c2sc(-c3cncc5nc6c7ccsc7c7sccc7c6nc53)cc2C4(c2ccc(C)cc2)c2ccc(C)cc2)cc1, and Acceptors: PC71BM? ->\", \"input\": \"\", \"output\": \" 2.2240313664507148\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1cc(C=C(C#N)C(=O)O)sc1-c1cc(C)c(-c2cc(C)c(-c3ccc(N(c4ccc5c(c4)C(C)(C)c4ccccc4-5)c4ccc5c(c4)C(C)(C)c4ccccc4-5)cc3)s2)s1, and Acceptors: TiO2? ->\", \"input\": \"\", \"output\": \" 2.332146171505\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : Cc1ccsc1-c1sc(-c2sc(C3=S=C(c4sccc4C)C(C)=C3)cc2C)c2nc3c(nc21)-c1cccc2cccc-3c12, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 1.1669230056659374\\n\"}, {\"instruction\": \"what is the power conversion efficiency of organic solar cells with donor : C[Si]1(C)c2ccccc2-c2ccc(-c3ccc(-c4ccc(C5=C(c6ccccc6)C(c6ccccc6)=C(c6ccc(-c7cccs7)s6)[Si]5(C)C)s4)s3)cc21, and Acceptors: PC61BM? ->\", \"input\": \"\", \"output\": \" 0.5621869589565295\\n\"}]"
  },
  {
    "path": "dataset/waterStability/convert.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 19,\n   \"id\": \"0498b113\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import pandas as pd\\n\",\n    \"import random\\n\",\n    \"\\n\",\n    \"df = pd.read_csv('waterStability.csv')\\n\",\n    \"# key=csv column name, value=slot in Q\\n\",\n    \"slot = {\\\"name\\\":\\\"name\\\", \\\"Activated formula unit\\\":\\\"activated formula unit\\\", \\\"confidence\\\":\\\"confidence\\\", \\\"stability\\\":\\\"water stability\\\"}\\n\",\n    \"pair = [(\\\"Activated formula unit\\\", \\\"name\\\"), (\\\"name\\\", \\\"stability\\\", \\\"confidence\\\")]\\n\",\n    \"data_list = []\\n\",\n    \"for df_slice in df.iterrows():\\n\",\n    \"    for p in pair:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        if len(p) != 3:\\n\",\n    \"            ran = random.randint(0,3)\\n\",\n    \"            if ran == 0:\\n\",\n    \"                question = \\\"What is \\\"+ slot[p[0]] + \\\" of given \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"            elif ran == 1:\\n\",\n    \"                question = \\\"Write \\\"+ slot[p[0]] + \\\" of given \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"            elif ran == 2:\\n\",\n    \"                question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"            elif ran == 3:\\n\",\n    \"                question = \\\"Tell me \\\"+ slot[p[0]] + \\\" of given \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"            answer = df_slice[1][p[0]]\\n\",\n    \"            input_ = df_slice[1][p[1]]\\n\",\n    \"        else:\\n\",\n    \"            ran = random.randint(0,3)\\n\",\n    \"            ran1 = random.randint(0,1)\\n\",\n    \"            if ran1 == 0:\\n\",\n    \"                cond = \\\" at room temperature and atmospheric pressure\\\"\\n\",\n    \"            else:\\n\",\n    \"                cond = \\\" at normal measurement conditions\\\"\\n\",\n    \"            if ran == 0:\\n\",\n    \"                question = \\\"How is the \\\" + slot[p[1]] + \\\"of given \\\"+ p[1] + cond + \\\"? ->\\\"\\n\",\n    \"            elif ran == 1:\\n\",\n    \"                question = \\\"Write \\\" + p[1] + \\\" of given \\\"+ slot[p[0]] + cond+ \\\". ->\\\"\\n\",\n    \"            elif ran == 2:\\n\",\n    \"                question = \\\"Given \\\" + p[0] + \\\", write its \\\"+ slot[p[1]] + cond+ \\\". ->\\\"\\n\",\n    \"            elif ran == 3:\\n\",\n    \"                question = \\\"Tell me \\\"+ slot[p[1]] + \\\" of given \\\"+ p[0] + cond+ \\\". ->\\\"                                                \\n\",\n    \"            answer = \\\" It has \\\" + str(df_slice[1][p[1]]) + \\\" water stability with \\\" + str(df_slice[1][p[2]]) + \\\" confidence.\\\" \\n\",\n    \"            input_ = df_slice[1][p[0]]\\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] =  \\\" \\\"+str(input_)+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" \\\"+str(answer)+\\\"\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 20,\n   \"id\": \"619c27ef\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"338\\n\",\n      \"6\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"# add unable to answer question\\n\",\n    \"print(len(data_list))\\n\",\n    \"add = int(len(data_list)/50)\\n\",\n    \"print(add)\\n\",\n    \"ran_list = random.sample(range(0,len(data_list)), add)\\n\",\n    \"for i, df_slice in enumerate(df.iterrows()):\\n\",\n    \"    if i in ran_list:\\n\",\n    \"        tmp_dict = {}\\n\",\n    \"        ran = random.randint(0,3)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"How is the \\\" + slot[p[1]] + \\\"of given \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write \\\" + p[1] + \\\" of given \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given \\\" + p[0] + \\\", write its \\\"+ slot[p[1]] + \\\". ->\\\"\\n\",\n    \"        elif ran == 3:\\n\",\n    \"            question = \\\"Tell me \\\"+ slot[p[1]] + \\\" of given \\\"+ p[0] + \\\". ->\\\"                                                \\n\",\n    \"        tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"        tmp_dict[\\\"input\\\"] = \\\" \\\"+str(df_slice[1][p[0]])+\\\"\\\\n\\\"\\n\",\n    \"        tmp_dict[\\\"output\\\"] = \\\" Unable to answer the question due to lack of conditions\\\\n\\\"\\n\",\n    \"        data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 21,\n   \"id\": \"166b1e11\",\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"342\\n\",\n      \"11\\n\",\n      \"['surname', 'use', 'knife', 'distance', 'governor', 'goal', 'house', 'bag', 'correspondent', 'calendar']\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"# https://github.com/psobko/Common-English-Nouns\\n\",\n    \"with open('../2325_nouns.json', 'r', encoding='utf-8') as f:\\n\",\n    \"    nouns = json.load(f)\\n\",\n    \"print(len(data_list))\\n\",\n    \"# add no-answer question according to length of data_list\\n\",\n    \"add = int(len(data_list)/30)\\n\",\n    \"print(add)\\n\",\n    \"add_nouns = random.sample(nouns, add)\\n\",\n    \"print(add_nouns[:10])\\n\",\n    \"for an in add_nouns:\\n\",\n    \"    ran_ = random.randint(0,1)\\n\",\n    \"    if ran_ == 0:\\n\",\n    \"        p = pair[0]\\n\",\n    \"    else:\\n\",\n    \"        p = pair[1]\\n\",\n    \"    tmp_dict = {}\\n\",\n    \"    if len(p) != 3:\\n\",\n    \"        ran = random.randint(0,3)\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"What is \\\"+ slot[p[0]] + \\\" of given \\\"+ p[1] + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write \\\"+ slot[p[0]] + \\\" of given \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given \\\" + p[1] + \\\", write its \\\"+ slot[p[0]] + \\\". ->\\\"\\n\",\n    \"        elif ran == 3:\\n\",\n    \"            question = \\\"Tell me \\\"+ slot[p[0]] + \\\" of given \\\"+ p[1] + \\\". ->\\\"\\n\",\n    \"        answer = an + \\\" has no \\\" + slot[p[0]] +\\\".\\\"\\n\",\n    \"    else:\\n\",\n    \"        ran = random.randint(0,3)\\n\",\n    \"        ran1 = random.randint(0,1)\\n\",\n    \"        if ran1 == 0:\\n\",\n    \"            cond = \\\" at room temperature and atmospheric pressure\\\"\\n\",\n    \"        else:\\n\",\n    \"            cond = \\\" at normal measurement conditions\\\"\\n\",\n    \"        if ran == 0:\\n\",\n    \"            question = \\\"How is the \\\" + slot[p[1]] + \\\"of given \\\"+ p[1] + cond + \\\"? ->\\\"\\n\",\n    \"        elif ran == 1:\\n\",\n    \"            question = \\\"Write \\\" + p[1] + \\\" of given \\\"+ slot[p[0]] + cond+ \\\". ->\\\"\\n\",\n    \"        elif ran == 2:\\n\",\n    \"            question = \\\"Given \\\" + p[0] + \\\", write its \\\"+ slot[p[1]] + cond+ \\\". ->\\\"\\n\",\n    \"        elif ran == 3:\\n\",\n    \"            question = \\\"Tell me \\\"+ slot[p[1]] + \\\" of given \\\"+ p[0] + cond+ \\\". ->\\\"                                                \\n\",\n    \"        answer = an + \\\" has no \\\"+slot[p[1]]+\\\".\\\" \\n\",\n    \"    tmp_dict[\\\"instruction\\\"] = question\\n\",\n    \"    tmp_dict[\\\"input\\\"] =  \\\" \\\"+an+\\\"\\\\n\\\"\\n\",\n    \"    tmp_dict[\\\"output\\\"] = \\\" \\\"+str(answer)+\\\"\\\\n\\\"\\n\",\n    \"    data_list.append(tmp_dict)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 22,\n   \"id\": \"101bf6e1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import json\\n\",\n    \"\\n\",\n    \"json_str = json.dumps(data_list, indent=4)\\n\",\n    \"with open('waterStability.json', 'w', encoding='utf-8') as json_file:\\n\",\n    \"    json_file.write(json_str)\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": null,\n   \"id\": \"e77195f1\",\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": []\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"Python 3\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.6.13\"\n  }\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 5\n}\n"
  },
  {
    "path": "dataset/waterStability/waterStability.csv",
    "content": "name,Activated formula unit,confidence,stability\nCo2(9H-purin-6-amine)2(oxalate)2,Co2(AD)2(C4H9CO2)2,high,high\n\"Cr3F(H2O)2O(1,4-benzenedicarboxylate)3\",Cr3F(H2O)2O(BDC)3,high,high\n\"Cr3F(H2O)2O(1,4-benzenedicarboxylate-SO3H)3\",Cr3F(H2O)2O(BDC-SO3H)3,high,high\n\"Al12O(OH)18(H2O)3(Al2(OH)4)(1,3,5-benzenetricarboxylate)6\",Al12O(OH)18(H2O)3(Al2(OH)4)(BTC)6,high,high\n\"Ni3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\",Ni3(BTP)2,high,high\nZn(2-methylimidazole)2,Zn(MEIM)2,high,high\nmeso-tetra(4-carboxyl-phenyl)porphyrin(AlOH)2,TCPP(AlOH)2,medium,high\n\"Cd(H(S)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate)2\",Cd(HTHIPC)2,medium,high\n\"Cu2(P,P′-diphenylmethylenediphosphinate)24,4′-bipyridine\",Cu2(PCP)2BIPY,medium,high\n\"Pb2(2-(5–6-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2(H2O)2\",Pb2(PTPTP)2(H2O)2,medium,high\n\"Pb2(p-phenylenediacetate)(2-(5–6-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2\",Pb2(p-PDA)(PTPTP)2,medium,high\n\"Pb4(o-phenylenediacetate)2(2-(5–6-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2\",Pb4(o-PDA)2(PTPTP)2,medium,high\n\"La(3,5-bis(2H-tetrazol-5-yl)-benzoate)H2O\",La(BTB)H2O,low,high\n\"H3(Cu4Cl)3(1,3,5-tris(1H-1,2,3-triazol-5-yl)benzene)8\",H3(Cu4Cl)3(BTTRI)8,low,high\n\"Zn(1,4-benzenedi(4-pyrazolyl))\",\"Zn(1,4-BDP)\",low,high\n\"Zn(1,3-benzenedi(4-pyrazolyl))\",\"Zn(1,3-BDP)\",low,high\n\"Cu3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\",Cu3(BTP)2,low,high\n\"Zn3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\",Zn3(BTP)2,low,high\n\"Al2(OH)2(biphenyl-3,3′,5,5′-tetracarboxylate)\",Al2(OH)2(H4L),low,high\n\"La(H51,2,4,5-tetrakisphosphonomethylbenzene)(H2O)4\",La(H5L5)(H2O)4,low,high\n\"Cu4(2,2-dimethylpropanoate)8(1,3,5,7-tetrakis(4-(2-ethyl-1H-imidazol-1-yl)phenyl)-ane)\",Cu4(Me3CCOO)8(TEIA),low,high\n\"Ba(tetraethyl-1,3,6,8-pyrenetetraphosponate)\",BaH2L,high,high\nAl(OH)(isophthalate),Al(OH)(ISO),high,high\n\"Hf6O6(OH)2(dithieno[3,2-b;2′,3′-d]-thiophene-2,6-dicarboxylate)4\",Hf6O6(OH)2(DTTDC)4,high,high\n\"Zr6O6(OH)2(dithieno[3,2-b;2′,3′-d]-thiophene-2,6-dicarboxylate)4\",Zr6O6(OH)2(DTTDC)4,high,high\n\"Zr6O6(OH)2(2,5-thiophenedicarboxylate)4\",Zr6O6(OH)2(TDC)4,high,high\n\"Ag(3,5-bis(trifluoromethyl)-1,2,4-triazolate)\",Ag(TZ),high,high\n\"Cr3F(H2O)2O(1,4-benzenedicarboxylate-NH2)3\",Cr3F(H2O)2O(BDC-NH2)3,high,high\n\"Ti8O8(OH)4(1,4-benzenedicarboxylate-NH2)6\",Ti8O8(OH)4(BDC-NH2)6,high,high\n\"Al(OH)(1,4-benzenedicarboxylate)\",Al(OH)(BDC),high,high\n\"Cr(OH)1,4-benzenedicarboxylate\",Cr(OH)BDC,high,high\nZr6O4(OH)4(meso-tetra(4-carboxyl-phenyl)porphyrin-H2)3,Zr6O4(OH)4(TCPP-H2)3,high,high\nZr6O8(H2O)8(meso-tetra(4-carboxyl-phenyl)porphyrin-H2)2,Zr6O8(H2O)8(TCPP-H2)2,high,high\nZr6O4(OH)4(fumarate)6,Zr6O4(OH)4(FUM)6,high,high\nZr6O4(OH)4(fumarate)6,Zr6O4(OH)4(FUM)6,high,high\nZr6O4(OH)4(fumarate)6,Zr6O4(OH)4(FUM)6,high,high\nZr6O4(OH)4(fumarate)6,Zr6O4(OH)4(FUM)6,high,high\n\"Zr6O4(OH)4(1H-pyrazole-3,5-dicarboxylate4)5(HCOO)2(H2O)2\",Zr6O4(OH)4(PZDC4)5(HCOO)2(H2O)2,high,high\n\"Zr6O4(OH)4(1,4-benzenedicarboxylate-(OH)2)6\",Zr6O4(OH)4(BDC-(OH)2)6,high,high\n\"Zr6O4(OH)4(4,4′,4″,4‴-methanetetrayltetrabenzoate)2(HCOO)4(H2O)4\",Zr6O4(OH)4(MTB)2(HCOO)4(H2O)4,high,high\nNi8(OH)4(H2O)2(1H-pyrazole-4-carboxylate)6,Ni8(OH)4(H2O)2(L6)6,high,high\n\"Ni8(OH)4(H2O)2(4,4′-benzene-1,4-diylbis(1H-pyrazole))6\",Ni8(OH)4(H2O)2(L8)6,high,high\n\"Ni8(OH)4(H2O)2(4,4′-buta-1,3-diyne-1,4-diylbis(1H-pyrazole))6\",Ni8(OH)4(H2O)2(L9)6,high,high\nNi8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0)6,Ni8(OH)4(H2O)2(L10)6,high,high\nNi8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0-(CH3)2)6,Ni8(OH)4(H2O)2(L10-(CH3)2)6,high,high\nNi8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0-(CF3)2)6,Ni8(OH)4(H2O)2(L10-(CF3)2)6,high,high\n\"Zn2(1,3,5-benzenetricarboxylate)(OH)-(H2O)\",Zn2(BTC)(OH)-(H2O),high,high\nZn(2-((pyridin-4-yl)methylamino)-4-methylpentanoate4)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate5),Zn(L14)(L15),high,high\n\"Zr6(OH)16(1,3,6,8-tetrakis(p-benzoate)pyrene)2\",Zr6(OH)16(TBAPY)2,high,high\nZr6O4(OH)4(OH)4(H2O)4(Mmeso-tetra(4-carboxyl-phenyl)porphyrin)2,Zr6O4(OH)4(OH)4(H2O)4(MTCPP)2,high,high\n\"Zr6O6(1,4-benzenedicarboxylate)12\",Zr6O6(BDC)12,high,high\n\"Zr6O6(1,4-benzenedicarboxylate-CH3)12\",Zr6O6(BDC-CH3)12,high,high\n\"Zr6O6(1,4-benzenedicarboxylate-NH2)12\",Zr6O6(BDC-NH2)12,high,high\n\"Zn2(1,4-9H-purin-6-amineC)2(4-diazabicyclo[2.2.2]-octane)\",\"Zn2(1,4-ADC)2(DABCO)\",high,high\n\"Zn2(1,4-benzenedicarboxylate-(CH3)4)2(4-diazabicyclo[2.2.2]-octane)\",Zn2(BDC-(CH3)4)2(DABCO),high,high\n\"Zn2(1,4-benzenedicarboxylate)2(4,4′-bipyridine)\",Zn2(BDC)2(BPY),high,high\n\"Zn2(1,4-benzenedicarboxylate)2(4,4′-bipyridine)\",Zn2(BDC)2(BPY),high,high\nZn2(Cyclohexylammonium)-tetrakis(μ3-phosphito),(C6H14N)2Zn3(HPO3)4,high,high\nAl(OH)(isophthalate-CH3),Al(OH)(ISO-CH3),medium,high\nAl(OH)(isophthalate-H),Al(OH)(ISO-H),medium,high\nAl(OH)(isophthalate-NH2),Al(OH)(ISO-NH2),medium,high\nAl(OH)(isophthalate-NO2),Al(OH)(ISO-NO2),medium,high\nAl(OH)(isophthalate-OCH3),Al(OH)(ISO-OCH3),medium,high\nAl(OH)(isophthalate-OH),Al(OH)(ISO-OH),medium,high\nCdZrSr(oxalate)4,CdZrSr(C2O4)4,medium,high\nCu2(PCN)2(H2O)2,Cu2(PCN)2(H2O)2,medium,high\nEuCu(Pyridine-3-carboxylate)2(oxalate),EuCu(NIC)2(C2O4),medium,high\n\"Al(OH)(1,4-benzenedicarboxylate-F)\",Al(OH)(BDC-F),medium,high\n\"Al(OH)(1,4-napthalenedicarboxylate)\",\"Al(OH)(1,4-NDC)\",medium,high\n\"Ni2(HFPDPT)-(4,4′-bipyridine)2(H2O)2](H2O)8\",Ni2(HFPDPT)-(BPY)2(H2O)2](H2O)8,medium,high\n\"Zr6O6(1,4-benzenedicarboxylate-Br)12\",Zr6O6(BDC-Br)12,medium,high\n\"Zr6O6(4,4′-biphenyldicarboxylate)12\",Zr6O6(BPDC)12,medium,high\n\"[KCo3(2-oxidopropane-1,2,3-tricarboxylate)(2-hydroxypropane-1,2,3-tricarboxylate)(H2O)28H2O]8\",[KCo3(C6H4O7)(C6H5O7)(H2O)28H2O]8,medium,high\nZn(phenyl benzimidazolate)2,Zn(PhIM)2,medium,high\nZn(phenyl benzimidazolate)2,Zn(PhIM)2,medium,high\nZn(phenyl benzimidazolate)2,Zn(PhIM)2,low,high\nZn(phenyl benzimidazolate)2,Zn(PhIM)2,low,high\nZn(ICA)2,Zn(ICA)2,medium,high\n\"Zn3(2,3,5-Triphenyltetrazolium chloride)(OH)2(H2O)\",Zn3(TTC)(OH)2(H2O),medium,high\n\"ZnCo(1,2,4,5-benzenetetracarboxylic acid)\",ZnCo(BTEC),medium,high\n\"Zr6O6(DM1,4-benzenedicarboxylate)12\",Zr6O6(DMBDC)12,medium,high\nZn(2-Aminopropanoate)(Cl),Zn(Ala)(Cl),low,high\nZn(2-Aminopropanoate)(OAc),Zn(Ala)(OAc),low,high\nCo2(9H-purin-6-amine)2(C3H7CO2)2,Co2(AD)2(C3H7CO2)2,low,high\n\"Hf6O6(OH)2(2,5-thiophenedicarboxylate)4\",Hf6O6(OH)2(TDC)4,low,high\n\"Hf6O6(OH)2(2,5-thiophenedicarboxylate)4.5\",Hf6O6(OH)2(TDC)4.5,low,high\n\"Zr6O6(OH)2(2,5-thiophenedicarboxylate)4.5\",Zr6O6(OH)2(TDC)4.5,low,high\n\"Zr6O4(OH)4(2,5-thiophenedicarboxylate)5\",Zr6O4(OH)4(TDC)5,low,high\n\"ZrO(1,4-benzenedicarboxylate)\",ZrO(BDC),low,high\n\"ZrO(2,6-napthalenedicarboxylate)\",\"ZrO(2,6-NDC)\",low,high\n\"ZrO(4,4′-biphenyldicarboxylate)\",ZrO(BPDC),low,high\n\"ZrO(4,4′-azobenzenedicarboxylate-Cl2)\",ZrO(ABDC-Cl2),low,high\nCu(2-((pyridin-4-yl)methylamino)-4-methylpentanoate1)(4-diazabicyclo[2.2.2]-octane)0.5,Cu(L11)(DABCO)0.5,low,high\n\"Ni-(1,2-bis(4-pyridyl)ethane)2(MoO4)\",Ni-(BPE)2(MoO4),low,high\n\"Zn6(imidazole-4,5-dicarboxylate)4(OH)2(Hpiperazine)2\",Zn6(IDC)4(OH)2(HPRZ)2,low,high\n\"Cd(2,6-napthalenedicarboxylate)0.5(PCA)\",\"Cd(2,6-NDC)0.5(PCA)\",low,high\nCd(2-((pyridin-4-yl)methylamino)-4-methylpentanoate)(Cl)(H2O),Cd(L1)(Cl)(H2O),low,high\nCd(2-(pyridin-4-yl)methylamino)-3-hydroxypropanoate)(Cl)(H2O),Cd(L2)(Cl)(H2O),low,high\nCd2(2-(pyridin-4-yl)methylamino)-3-hydroxypropanoate)2(Br)2(H2O)3,Cd2(L2)2(Br)2(H2O)3,low,high\nCd(2-((pyridin-4-yl)methylamino)-3-hydroxybutanoate)(Cl)(H2O)2,Cd(L3)(Cl)(H2O)2,low,high\n\"Zn24,4′-bipyridine-2,6,2′,6′-tetracarboxylate\",Zn2L4,low,high\n\"Ni(4-(1,2,4-triazol-4-yl)phenylphosphonate))2\",Ni(HPTZ)2,low,high\n\"Zn4O(2,2′-bis-trifluoromethyl-biphenyl-4,4′-dicarboxylate)3(4,4′-bipyridine)0.5(H2O)\",Zn4O(BFBPDC)3(BPY)0.5(H2O),low,high\nNi(2-((pyridin-4-yl)methylamino)-4-methylpentanoate3)2,Ni(L13)2,low,high\nCo(2-((pyridin-4-yl)methylamino)-4-methylpentanoate3)2,Co(L13)2,low,high\nNi2(oxalate)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate6)2,Ni2(C2O4)(L16)2,low,high\n\"Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH3)2)3\",Zr3O2(OH)2(TPDC-(CH3)2)3,low,high\n\"Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH3)4)3\",Zr3O2(OH)2(TPDC-(CH3)4)3,low,high\n\"Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH2N3)4)3\",Zr3O2(OH)2(TPDC-(CH2N3)4)3,low,high\n\"Cu(4,4′-dipyridylacetylene)2(SiF6)\",Cu(DPA)2(SiF6),low,high\n\"Zr6O6(1,4-napthalenedicarboxylate)12\",\"Zr6O6(1,4-NDC)12\",low,high\n\"Zr6O6(2,6-napthalenedicarboxylate)12\",\"Zr6O6(2,6-NDC)12\",low,high\n\"Zr6O6(1,4-benzenedicarboxylate-(CO2H)2)12\",Zr6O6(BDC-(CO2H)2)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-(OMe)2)12\",Zr6O6(BDC-(OMe)2)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-Br2)12\",Zr6O6(BDC-Br2)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-CF3)12\",Zr6O6(BDC-CF3)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-Cl2)12\",Zr6O6(BDC-Cl2)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-CO2H)12\",Zr6O6(BDC-CO2H)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-(CH3)2)12\",Zr6O6(BDC-(CH3)2)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-I)12\",Zr6O6(BDC-I)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-NO2)12\",Zr6O6(BDC-NO2)12,low,high\n\"Zr6O6(1,4-benzenedicarboxylate-SO3H)12\",Zr6O6(BDC-SO3H)12,low,high\n\"Cu3(biphenyl-3,4′,5-tricarboxylate)\",Cu3(BHTC),low,high\nZn(2-Amino-3-methylbutanoic acid)(Cl),Zn(VAL)(Cl),low,high\nZn(2-Amino-3-methylbutanoic acid)(formate),Zn(VAL)(FOR),low,high\n\"Zn2(1,4-benzenedicarboxylate-(NO2)2)2(4-diazabicyclo[2.2.2]-octane)\",Zn2(BDC-(NO2)2)2(DABCO),low,high\n\"Zn(1,4,5,8-Naphthalenediimid)\",Zn(NDI-H),low,high\nZr6O6(fumarate)12,Zr6O6(FUM)12,low,high\n\"Al13(OH)27(H2O)6(1,4-benzenedicarboxylate-NH2)3Cl6\",Al13(OH)27(H2O)6(BDC-NH2)3Cl6,high,low\n\"Co2(2,5-dihydroxyterephthalate)\",Co2(DOBDC),high,low\n\"Cu3(1,3,5-benzenetricarboxylate)2\",Cu3(BTC)2,high,low\n\"Mg2(2,5-dihydroxyterephthalate)\",Mg2(DOBDC),high,low\n\"Cr3F(H2O)2O(1,4-benzenedicarboxylate-NO2)3\",Cr3F(H2O)2O(BDC-NO2)3,high,low\n\"V(O)(1,4-benzenedicarboxylate-F)\",V(O)(BDC-F),high,low\n\"Al(OH)(2,6-napthalenedicarboxylate)\",\"Al(OH)(2,6-NDC)\",high,low\n\"Cu3(3,5-bis(2H-tetrazol-5-yl)-benzoate)2(H2O)3\",Cu3(BTB)2(H2O)3,high,low\n\"Zr6O4(OH)4(2,6-napthalenedicarboxylate-(OH)2)6\",\"Zr6O4(OH)4(2,6-NDC-(OH)2)6\",high,low\n\"Zr6O4(OH)4(4,4′-biphenyldicarboxylate-(OH)2)6\",Zr6O4(OH)4(BPDC-(OH)2)6,high,low\n\"Zr6O4(OH)4(1,3,5-benzenetricarboxylate)2(HCOO)6\",Zr6O4(OH)4(BTC)2(HCOO)6,high,low\nNi8(OH)4(H2O)2(4-(1H-pyrazole-4-yl)benzoate)6,Ni8(OH)4(H2O)2(L7)6,high,low\n\"Ni2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\",Ni2(BDC)2(DABCO),high,low\n\"Ni2(2,5-dihydroxyterephthalate)\",Ni2(DOBDC),high,low\n\"Zn2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\",Zn2(BDC)2(DABCO),high,low\n\"Zn2(1,4-napthalenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\",\"Zn2(1,4-NDC)2(DABCO)\",high,low\n\"Zn2(1,4-benzenedicarboxylate)(1,4-benzenedicarboxylate-(CH3)4)(4-diazabicyclo[2.2.2]-octane)\",Zn2(BDC)(BDC-(CH3)4)(DABCO),high,low\n\"Zn2(2,5-dihydroxyterephthalate)\",Zn2(DOBDC),high,low\n\"Zn2(2,6-napthalenedicarboxylate)2(4,4′-bipyridine)\",\"Zn2(2,6-NDC)2(BPY)\",high,low\n\"Co2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\",Co2(BDC)2(DABCO),medium,low\n\"Cu2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\",Cu2(BDC)2(DABCO),medium,low\n\"Zn4O(1,4-benzenedicarboxylate-2-CF3O)3\",Zn4O(BDC-2-CF3O)3,medium,low\n\"Cu3(1,3,5-benzenetricarboxylate-(CH3)2)2(H2O)3\",Cu3(BTC-(CH3)2)2(H2O)3,low,low\n\"Cu(4,4′-hexafluoroisopropylidene-bis-benzoate)(H24,4′-hexafluoroisopropylidene-bis-benzoate)0.5\",Cu(HFIPBB)(H2HFIPBB)0.5,low,low\n\"Cu3(1,3,5-benzenetricarboxylate-CH3)2(H2O)3\",Cu3(BTC-CH3)2(H2O)3,low,low\n\"Zn4O(1,4-benzenedicarboxylate-(CH3)2)3\",Zn4O(BDC-(CH3)2)3,low,low\n\"Zn4O(1,4-benzenedicarboxylate-CH3)3\",Zn4O(BDC-CH3)3,low,low\n\"Zn4O(1,4-benzenedicarboxylate-NH-CO-(CH2)14CH3)\",Zn4O(BDC-NH-CO-(CH2)14CH3),low,low\n\"Zn4O(1,4-benzenedicarboxylate-NH2)3\",Zn4O(BDC-NH2)3,low,low\n\"Al8(OH)12(OH)3(H2O)3(1,3,5-benzenetricarboxylate)3\",Al8(OH)12(OH)3(H2O)3(BTC)3,low,low\n\"Ti8O8(OH)4(1,4-benzenedicarboxylate)6\",Ti8O8(OH)4(BDC)6,low,low\nCu(CH3OH)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate1),Cu(CH3OH)(L11),low,low\nCuO(2-((pyridin-4-yl)methylamino)-4-methylpentanoate2),CuO(L12),low,low\n\"Cu2(2′,5′-dialkyloxy-[1,1′:4′,1″-terphenyl]-3,3″,5,5″-tetracarboxylate-(ethyl))\",Cu2(TPTC-O-(ethyl)),low,low\n\"Cu2(2′,5′-dialkyloxy-[1,1′:4′,1″-terphenyl]-3,3″,5,5″-tetracarboxylate-(n-propyl))\",Cu2(TPTC-O-(n-propyl)),low,low\n\"Cu2(2′,5′-dialkyloxy-[1,1′:4′,1″-terphenyl]-3,3″,5,5″-tetracarboxylate-(n-hexyl))\",Cu2(TPTC-O-(n-hexyl)),low,low\nZn(pyrazine)2(SiF6),Zn(PYR)2(SiF6),low,low\n\"Zr6O6(1,4-benzenedicarboxylate-F2)12\",Zr6O6(BDC-F2)12,low,low\n\"Zr6O6(1,4-benzenedicarboxylate-F)12\",Zr6O6(BDC-F)12,low,low\n\"Zr6O6(4,4′-azobenzenedicarboxylate-Cl2)12\",Zr6O6(ABDC-Cl2)12,low,low\n\"Zr6O6(4,4′-azobenzenedicarboxylate)12\",Zr6O6(ABDC)12,low,low\n"
  },
  {
    "path": "dataset/waterStability/waterStability.json",
    "content": "[\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" meso-tetra(4-carboxyl-phenyl)porphyrin(AlOH)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn(pyrazine)2(SiF6)\\n\",\n        \"output\": \" Zn(PYR)2(SiF6)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(4,4\\u2032-azobenzenedicarboxylate)12\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" CuO(2-((pyridin-4-yl)methylamino)-4-methylpentanoate2)\\n\",\n        \"output\": \" CuO(L12)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0-(CH3)2)6\\n\",\n        \"output\": \" Ni8(OH)4(H2O)2(L10-(CH3)2)6\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Cu2(PCN)2(H2O)2\\n\",\n        \"output\": \" Cu2(PCN)2(H2O)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Al(OH)(isophthalate-OH)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Cu3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" La(3,5-bis(2H-tetrazol-5-yl)-benzoate)H2O\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O6(OH)2(2,5-thiophenedicarboxylate)4\\n\",\n        \"output\": \" Zr6O6(OH)2(TDC)4\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" silk\\n\",\n        \"output\": \" silk has no water stability.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(2,6-napthalenedicarboxylate)\\n\",\n        \"output\": \" Al(OH)(2,6-NDC)\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" V(O)(1,4-benzenedicarboxylate-F)\\n\",\n        \"output\": \" V(O)(BDC-F)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Mg2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cu3(1,3,5-benzenetricarboxylate)2\\n\",\n        \"output\": \" Cu3(BTC)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn(2-Amino-3-methylbutanoic acid)(formate)\\n\",\n        \"output\": \" Zn(VAL)(FOR)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" door\\n\",\n        \"output\": \" door has no water stability.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Pb2(p-phenylenediacetate)(2-(5\\u20136-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2\\n\",\n        \"output\": \" Pb2(p-PDA)(PTPTP)2\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" ZrO(4,4\\u2032-biphenyldicarboxylate)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH3)2)3\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)2(4,4\\u2032-bipyridine)\\n\",\n        \"output\": \" Zn2(BDC)2(BPY)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn(ICA)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zr6O6(fumarate)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-F2)12\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(4,4\\u2032-biphenyldicarboxylate-(OH)2)6\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Cu2(2\\u2032,5\\u2032-dialkyloxy-[1,1\\u2032:4\\u2032,1\\u2033-terphenyl]-3,3\\u2033,5,5\\u2033-tetracarboxylate-(ethyl))\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn(1,4,5,8-Naphthalenediimid)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(4-(1H-pyrazole-4-yl)benzoate)6\\n\",\n        \"output\": \" Ni8(OH)4(H2O)2(L7)6\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(4,4\\u2032-benzene-1,4-diylbis(1H-pyrazole))6\\n\",\n        \"output\": \" Ni8(OH)4(H2O)2(L8)6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\\n\",\n        \"output\": \" Zn3(BTP)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Cd(2-(pyridin-4-yl)methylamino)-3-hydroxypropanoate)(Cl)(H2O)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O6(OH)2(2,5-thiophenedicarboxylate)4.5\\n\",\n        \"output\": \" Zr6O6(OH)2(TDC)4.5\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(OH)2(dithieno[3,2-b;2\\u2032,3\\u2032-d]-thiophene-2,6-dicarboxylate)4\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-NH-CO-(CH2)14CH3)\\n\",\n        \"output\": \" Zn4O(BDC-NH-CO-(CH2)14CH3)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Al8(OH)12(OH)3(H2O)3(1,3,5-benzenetricarboxylate)3\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn(2-Aminopropanoate)(Cl)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(isophthalate-CH3)\\n\",\n        \"output\": \" Al(OH)(ISO-CH3)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Al(OH)(1,4-napthalenedicarboxylate)\\n\",\n        \"output\": \" Al(OH)(1,4-NDC)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-I)12\\n\",\n        \"output\": \" Zr6O6(BDC-I)12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Cu3(biphenyl-3,4\\u2032,5-tricarboxylate)\\n\",\n        \"output\": \" Cu3(BHTC)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Mg2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \" Mg2(DOBDC)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(4,4\\u2032-azobenzenedicarboxylate-Cl2)12\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" client\\n\",\n        \"output\": \" client has no water stability.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zr6(OH)16(1,3,6,8-tetrakis(p-benzoate)pyrene)2\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Pb2(2-(5\\u20136-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2(H2O)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Ti8O8(OH)4(1,4-benzenedicarboxylate-NH2)6\\n\",\n        \"output\": \" Ti8O8(OH)4(BDC-NH2)6\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" CuO(2-((pyridin-4-yl)methylamino)-4-methylpentanoate2)\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" zebra\\n\",\n        \"output\": \" zebra has no activated formula unit.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Cd(2,6-napthalenedicarboxylate)0.5(PCA)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-(OMe)2)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Al(OH)(isophthalate-NH2)\\n\",\n        \"output\": \" Al(OH)(ISO-NH2)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zr6O6(1,4-napthalenedicarboxylate)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Cu(2-((pyridin-4-yl)methylamino)-4-methylpentanoate1)(4-diazabicyclo[2.2.2]-octane)0.5\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-CO2H)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability. ->\",\n        \"input\": \" Co2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(4,4\\u2032-azobenzenedicarboxylate)12\\n\",\n        \"output\": \" Zr6O6(ABDC)12\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Cu2(P,P\\u2032-diphenylmethylenediphosphinate)24,4\\u2032-bipyridine\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Ni(4-(1,2,4-triazol-4-yl)phenylphosphonate))2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Zn2(BDC)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate-(CH3)4)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Cu2(2\\u2032,5\\u2032-dialkyloxy-[1,1\\u2032:4\\u2032,1\\u2033-terphenyl]-3,3\\u2033,5,5\\u2033-tetracarboxylate-(n-hexyl))\\n\",\n        \"output\": \" Cu2(TPTC-O-(n-hexyl))\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(4,4\\u2032-benzene-1,4-diylbis(1H-pyrazole))6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Al(OH)(1,4-benzenedicarboxylate)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-SO3H)12\\n\",\n        \"output\": \" Zr6O6(BDC-SO3H)12\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" ZrO(2,6-napthalenedicarboxylate)\\n\",\n        \"output\": \" ZrO(2,6-NDC)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(fumarate)12\\n\",\n        \"output\": \" Zr6O6(FUM)12\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ni(4-(1,2,4-triazol-4-yl)phenylphosphonate))2\\n\",\n        \"output\": \" Ni(HPTZ)2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Al(OH)(isophthalate-CH3)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zn2(Cyclohexylammonium)-tetrakis(\\u03bc3-phosphito)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-Br)12\\n\",\n        \"output\": \" Zr6O6(BDC-Br)12\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Ni2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)2(4,4\\u2032-bipyridine)\\n\",\n        \"output\": \" Zn2(BDC)2(BPY)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Cr(OH)1,4-benzenedicarboxylate\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" ZrO(4,4\\u2032-azobenzenedicarboxylate-Cl2)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(4,4\\u2032-biphenyldicarboxylate)12\\n\",\n        \"output\": \" Zr6O6(BPDC)12\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Co2(9H-purin-6-amine)2(oxalate)2\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-NH-CO-(CH2)14CH3)\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(DM1,4-benzenedicarboxylate)12\\n\",\n        \"output\": \" Zr6O6(DMBDC)12\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate-NO2)3\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Pb2(2-(5\\u20136-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2(H2O)2\\n\",\n        \"output\": \" Pb2(PTPTP)2(H2O)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Cu2(2\\u2032,5\\u2032-dialkyloxy-[1,1\\u2032:4\\u2032,1\\u2033-terphenyl]-3,3\\u2033,5,5\\u2033-tetracarboxylate-(n-propyl))\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Ni2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Ni2(BDC)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Ni3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\\n\",\n        \"output\": \" Ni3(BTP)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0-(CH3)2)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \" Zr6O4(OH)4(FUM)6\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-(CO2H)2)12\\n\",\n        \"output\": \" Zr6O6(BDC-(CO2H)2)12\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ni2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(DM1,4-benzenedicarboxylate)12\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-Br2)12\\n\",\n        \"output\": \" Zr6O6(BDC-Br2)12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn(1,4-benzenedi(4-pyrazolyl))\\n\",\n        \"output\": \" Zn(1,4-BDP)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Al13(OH)27(H2O)6(1,4-benzenedicarboxylate-NH2)3Cl6\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Cu3(1,3,5-benzenetricarboxylate-CH3)2(H2O)3\\n\",\n        \"output\": \" Cu3(BTC-CH3)2(H2O)3\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-2-CF3O)3\\n\",\n        \"output\": \" Zn4O(BDC-2-CF3O)3\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \" Zr6O4(OH)4(FUM)6\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al2(OH)2(biphenyl-3,3\\u2032,5,5\\u2032-tetracarboxylate)\\n\",\n        \"output\": \" Al2(OH)2(H4L)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cu(CH3OH)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate1)\\n\",\n        \"output\": \" Cu(CH3OH)(L11)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate)12\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Ag(3,5-bis(trifluoromethyl)-1,2,4-triazolate)\\n\",\n        \"output\": \" Ag(TZ)\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-CH3)12\\n\",\n        \"output\": \" Zr6O6(BDC-CH3)12\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate-(CH3)4)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Zn2(BDC-(CH3)4)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" store\\n\",\n        \"output\": \" store has no activated formula unit.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH2N3)4)3\\n\",\n        \"output\": \" Zr3O2(OH)2(TPDC-(CH2N3)4)3\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O4(OH)4(meso-tetra(4-carboxyl-phenyl)porphyrin-H2)3\\n\",\n        \"output\": \" Zr6O4(OH)4(TCPP-H2)3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Al(OH)(isophthalate-H)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" La(H51,2,4,5-tetrakisphosphonomethylbenzene)(H2O)4\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cu2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has low water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \" Zn(PhIM)2\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)2(4,4\\u2032-bipyridine)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \" Zn2(DOBDC)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Cu(4,4\\u2032-dipyridylacetylene)2(SiF6)\\n\",\n        \"output\": \" Cu(DPA)2(SiF6)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-(CH3)2)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(1H-pyrazole-4-carboxylate)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" ZrO(2,6-napthalenedicarboxylate)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Zr6O6(4,4\\u2032-biphenyldicarboxylate)12\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zn4O(2,2\\u2032-bis-trifluoromethyl-biphenyl-4,4\\u2032-dicarboxylate)3(4,4\\u2032-bipyridine)0.5(H2O)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(OH)2(2,5-thiophenedicarboxylate)4.5\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" afternoon\\n\",\n        \"output\": \" afternoon has no water stability.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-CH3)3\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Cu2(PCN)2(H2O)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Al2(OH)2(biphenyl-3,3\\u2032,5,5\\u2032-tetracarboxylate)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Pb2(p-phenylenediacetate)(2-(5\\u20136-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O6(2,6-napthalenedicarboxylate)12\\n\",\n        \"output\": \" Zr6O6(2,6-NDC)12\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al13(OH)27(H2O)6(1,4-benzenedicarboxylate-NH2)3Cl6\\n\",\n        \"output\": \" Al13(OH)27(H2O)6(BDC-NH2)3Cl6\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(1H-pyrazole-3,5-dicarboxylate4)5(HCOO)2(H2O)2\\n\",\n        \"output\": \" Zr6O4(OH)4(PZDC4)5(HCOO)2(H2O)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cd(2-((pyridin-4-yl)methylamino)-3-hydroxybutanoate)(Cl)(H2O)2\\n\",\n        \"output\": \" Cd(L3)(Cl)(H2O)2\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Co2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has low water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O8(H2O)8(meso-tetra(4-carboxyl-phenyl)porphyrin-H2)2\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cu(4,4\\u2032-hexafluoroisopropylidene-bis-benzoate)(H24,4\\u2032-hexafluoroisopropylidene-bis-benzoate)0.5\\n\",\n        \"output\": \" Cu(HFIPBB)(H2HFIPBB)0.5\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Al(OH)(isophthalate-H)\\n\",\n        \"output\": \" Al(OH)(ISO-H)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)(1,4-benzenedicarboxylate-(CH3)4)(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" CdZrSr(oxalate)4\\n\",\n        \"output\": \" CdZrSr(C2O4)4\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cu3(1,3,5-benzenetricarboxylate)2\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn(2-((pyridin-4-yl)methylamino)-4-methylpentanoate4)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate5)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(isophthalate-OCH3)\\n\",\n        \"output\": \" Al(OH)(ISO-OCH3)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O4(OH)4(OH)4(H2O)4(Mmeso-tetra(4-carboxyl-phenyl)porphyrin)2\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(4,4\\u2032-buta-1,3-diyne-1,4-diylbis(1H-pyrazole))6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6(OH)16(1,3,6,8-tetrakis(p-benzoate)pyrene)2\\n\",\n        \"output\": \" Zr6(OH)16(TBAPY)2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-Cl2)12\\n\",\n        \"output\": \" Zr6O6(BDC-Cl2)12\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \" Zr6O4(OH)4(FUM)6\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Cd(H(S)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate)2\\n\",\n        \"output\": \" Cd(HTHIPC)2\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(4,4\\u2032-azobenzenedicarboxylate-Cl2)12\\n\",\n        \"output\": \" Zr6O6(ABDC-Cl2)12\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ti8O8(OH)4(1,4-benzenedicarboxylate)6\\n\",\n        \"output\": \" Ti8O8(OH)4(BDC)6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" La(H51,2,4,5-tetrakisphosphonomethylbenzene)(H2O)4\\n\",\n        \"output\": \" La(H5L5)(H2O)4\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(isophthalate-NO2)\\n\",\n        \"output\": \" Al(OH)(ISO-NO2)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" ZrO(1,4-benzenedicarboxylate)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(2,6-napthalenedicarboxylate)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Hf6O6(OH)2(dithieno[3,2-b;2\\u2032,3\\u2032-d]-thiophene-2,6-dicarboxylate)4\\n\",\n        \"output\": \" Hf6O6(OH)2(DTTDC)4\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-I)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zn3(2,3,5-Triphenyltetrazolium chloride)(OH)2(H2O)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zn(2-methylimidazole)2\\n\",\n        \"output\": \" Zn(MEIM)2\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Co2(9H-purin-6-amine)2(C3H7CO2)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zn2(1,4-napthalenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Zn2(1,4-NDC)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(2,6-napthalenedicarboxylate-(OH)2)6\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate-NH2)3\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" icon\\n\",\n        \"output\": \" icon has no activated formula unit.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O4(OH)4(1H-pyrazole-3,5-dicarboxylate4)5(HCOO)2(H2O)2\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cu3(3,5-bis(2H-tetrazol-5-yl)-benzoate)2(H2O)3\\n\",\n        \"output\": \" Cu3(BTB)2(H2O)3\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \" Zn(PhIM)2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cd(2-((pyridin-4-yl)methylamino)-3-hydroxybutanoate)(Cl)(H2O)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Co(2-((pyridin-4-yl)methylamino)-4-methylpentanoate3)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Ag(3,5-bis(trifluoromethyl)-1,2,4-triazolate)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Hf6O6(OH)2(2,5-thiophenedicarboxylate)4\\n\",\n        \"output\": \" Hf6O6(OH)2(TDC)4\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn(2-methylimidazole)2\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(2,5-thiophenedicarboxylate)5\\n\",\n        \"output\": \" Zr6O4(OH)4(TDC)5\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-CF3)12\\n\",\n        \"output\": \" Zr6O6(BDC-CF3)12\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-NO2)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(1H-pyrazole-4-carboxylate)6\\n\",\n        \"output\": \" Ni8(OH)4(H2O)2(L6)6\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Cu2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Cu2(BDC)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability? ->\",\n        \"input\": \" Zn24,4\\u2032-bipyridine-2,6,2\\u2032,6\\u2032-tetracarboxylate\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Cd(H(S)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cd2(2-(pyridin-4-yl)methylamino)-3-hydroxypropanoate)2(Br)2(H2O)3\\n\",\n        \"output\": \" Cd2(L2)2(Br)2(H2O)3\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Cr(OH)1,4-benzenedicarboxylate\\n\",\n        \"output\": \" Cr(OH)BDC\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Pb4(o-phenylenediacetate)2(2-(5\\u20136-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn6(imidazole-4,5-dicarboxylate)4(OH)2(Hpiperazine)2\\n\",\n        \"output\": \" Zn6(IDC)4(OH)2(HPRZ)2\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-CH3)3\\n\",\n        \"output\": \" Zn4O(BDC-CH3)3\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Cd(2-((pyridin-4-yl)methylamino)-4-methylpentanoate)(Cl)(H2O)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cd(2-((pyridin-4-yl)methylamino)-4-methylpentanoate)(Cl)(H2O)\\n\",\n        \"output\": \" Cd(L1)(Cl)(H2O)\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O4(OH)4(4,4\\u2032,4\\u2033,4\\u2034-methanetetrayltetrabenzoate)2(HCOO)4(H2O)4\\n\",\n        \"output\": \" Zr6O4(OH)4(MTB)2(HCOO)4(H2O)4\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(4,4\\u2032-biphenyldicarboxylate-(OH)2)6\\n\",\n        \"output\": \" Zr6O4(OH)4(BPDC-(OH)2)6\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Cd(2-(pyridin-4-yl)methylamino)-3-hydroxypropanoate)(Cl)(H2O)\\n\",\n        \"output\": \" Cd(L2)(Cl)(H2O)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn(1,4,5,8-Naphthalenediimid)\\n\",\n        \"output\": \" Zn(NDI-H)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" EuCu(Pyridine-3-carboxylate)2(oxalate)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(4,4\\u2032-buta-1,3-diyne-1,4-diylbis(1H-pyrazole))6\\n\",\n        \"output\": \" Ni8(OH)4(H2O)2(L9)6\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-F2)12\\n\",\n        \"output\": \" Zr6O6(BDC-F2)12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn2(2,6-napthalenedicarboxylate)2(4,4\\u2032-bipyridine)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zn2(1,3,5-benzenetricarboxylate)(OH)-(H2O)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH3)2)3\\n\",\n        \"output\": \" Zr3O2(OH)2(TPDC-(CH3)2)3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Hf6O6(OH)2(2,5-thiophenedicarboxylate)4.5\\n\",\n        \"output\": \" Hf6O6(OH)2(TDC)4.5\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(1,3,5-benzenetricarboxylate)2(HCOO)6\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate)3\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cu3(3,5-bis(2H-tetrazol-5-yl)-benzoate)2(H2O)3\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)(1,4-benzenedicarboxylate-(CH3)4)(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Zn2(BDC)(BDC-(CH3)4)(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(1,4-benzenedicarboxylate-F)\\n\",\n        \"output\": \" Al(OH)(BDC-F)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(isophthalate-OH)\\n\",\n        \"output\": \" Al(OH)(ISO-OH)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" rod\\n\",\n        \"output\": \" rod has no water stability.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Ti8O8(OH)4(1,4-benzenedicarboxylate-NH2)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn(pyrazine)2(SiF6)\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Al(OH)(isophthalate)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-NO2)12\\n\",\n        \"output\": \" Zr6O6(BDC-NO2)12\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" stomach\\n\",\n        \"output\": \" stomach has no water stability.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn(2-Amino-3-methylbutanoic acid)(formate)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate)3\\n\",\n        \"output\": \" Cr3F(H2O)2O(BDC)3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate-SO3H)3\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn24,4\\u2032-bipyridine-2,6,2\\u2032,6\\u2032-tetracarboxylate\\n\",\n        \"output\": \" Zn2L4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-2-CF3O)3\\n\",\n        \"output\": \"  It has low water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(isophthalate)\\n\",\n        \"output\": \" Al(OH)(ISO)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ni-(1,2-bis(4-pyridyl)ethane)2(MoO4)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate)12\\n\",\n        \"output\": \" Zr6O6(BDC)12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" ZrO(4,4\\u2032-biphenyldicarboxylate)\\n\",\n        \"output\": \" ZrO(BPDC)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zn(1,3-benzenedi(4-pyrazolyl))\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate-(NO2)2)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Co2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \" Co2(DOBDC)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0)6\\n\",\n        \"output\": \" Ni8(OH)4(H2O)2(L10)6\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH2N3)4)3\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-Cl2)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate-NH2)3\\n\",\n        \"output\": \" Cr3F(H2O)2O(BDC-NH2)3\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cu(CH3OH)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate1)\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-SO3H)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Cu3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\\n\",\n        \"output\": \" Cu3(BTP)2\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" ZrO(4,4\\u2032-azobenzenedicarboxylate-Cl2)\\n\",\n        \"output\": \" ZrO(ABDC-Cl2)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Al(OH)(isophthalate-NO2)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Pb4(o-phenylenediacetate)2(2-(5\\u20136-[5-(pyrazin-2-yl)-1H-1,2,4-triazol-3-yl]-pyridin-2-yl-1H-1,2,4-triazol-3-yl)pyridine)2\\n\",\n        \"output\": \" Pb4(o-PDA)2(PTPTP)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability. ->\",\n        \"input\": \" Cu(4,4\\u2032-dipyridylacetylene)2(SiF6)\\n\",\n        \"output\": \" Unable to answer the question due to lack of conditions\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0-(CF3)2)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Cu3(1,3,5-benzenetricarboxylate-(CH3)2)2(H2O)3\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH3)4)3\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-Br)12\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ni2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \" Ni2(DOBDC)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Cu(4,4\\u2032-dipyridylacetylene)2(SiF6)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Al(OH)(isophthalate-NH2)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Ba(tetraethyl-1,3,6,8-pyrenetetraphosponate)\\n\",\n        \"output\": \" BaH2L\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Al8(OH)12(OH)3(H2O)3(1,3,5-benzenetricarboxylate)3\\n\",\n        \"output\": \" Al8(OH)12(OH)3(H2O)3(BTC)3\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Ni2(HFPDPT)-(4,4\\u2032-bipyridine)2(H2O)2](H2O)8\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" meso-tetra(4-carboxyl-phenyl)porphyrin(AlOH)2\\n\",\n        \"output\": \" TCPP(AlOH)2\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Al12O(OH)18(H2O)3(Al2(OH)4)(1,3,5-benzenetricarboxylate)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Al(OH)(isophthalate-OCH3)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Zn24,4\\u2032-bipyridine-2,6,2\\u2032,6\\u2032-tetracarboxylate\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn2(Cyclohexylammonium)-tetrakis(\\u03bc3-phosphito)\\n\",\n        \"output\": \" (C6H14N)2Zn3(HPO3)4\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-CO2H)12\\n\",\n        \"output\": \" Zr6O6(BDC-CO2H)12\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ba(tetraethyl-1,3,6,8-pyrenetetraphosponate)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Al(OH)(1,4-napthalenedicarboxylate)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate-(NO2)2)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Zn2(BDC-(NO2)2)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" ZnCo(1,2,4,5-benzenetetracarboxylic acid)\\n\",\n        \"output\": \" ZnCo(BTEC)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" H3(Cu4Cl)3(1,3,5-tris(1H-1,2,3-triazol-5-yl)benzene)8\\n\",\n        \"output\": \" H3(Cu4Cl)3(BTTRI)8\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-Br2)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Co2(9H-purin-6-amine)2(C3H7CO2)2\\n\",\n        \"output\": \" Co2(AD)2(C3H7CO2)2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(fumarate)6\\n\",\n        \"output\": \" Zr6O4(OH)4(FUM)6\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn2(1,4-9H-purin-6-amineC)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Zn2(1,4-ADC)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Cu3(1,3,5-benzenetricarboxylate-(CH3)2)2(H2O)3\\n\",\n        \"output\": \" Cu3(BTC-(CH3)2)2(H2O)3\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" ZnCo(1,2,4,5-benzenetetracarboxylic acid)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn2(1,4-9H-purin-6-amineC)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O6(OH)2(dithieno[3,2-b;2\\u2032,3\\u2032-d]-thiophene-2,6-dicarboxylate)4\\n\",\n        \"output\": \" Zr6O6(OH)2(DTTDC)4\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Cu2(2\\u2032,5\\u2032-dialkyloxy-[1,1\\u2032:4\\u2032,1\\u2033-terphenyl]-3,3\\u2033,5,5\\u2033-tetracarboxylate-(n-propyl))\\n\",\n        \"output\": \" Cu2(TPTC-O-(n-propyl))\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(4-(1H-pyrazole-4-yl)benzoate)6\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate-SO3H)3\\n\",\n        \"output\": \" Cr3F(H2O)2O(BDC-SO3H)3\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cu(2-((pyridin-4-yl)methylamino)-4-methylpentanoate1)(4-diazabicyclo[2.2.2]-octane)0.5\\n\",\n        \"output\": \" Cu(L11)(DABCO)0.5\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cr3F(H2O)2O(1,4-benzenedicarboxylate-NO2)3\\n\",\n        \"output\": \" Cr3F(H2O)2O(BDC-NO2)3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ni(2-((pyridin-4-yl)methylamino)-4-methylpentanoate3)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-F)12\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Co2(9H-purin-6-amine)2(oxalate)2\\n\",\n        \"output\": \" Co2(AD)2(C4H9CO2)2\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \" Zn(PhIM)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ni3(1,3,5-tris(1H-pyrazol-4-yl)benzene)2\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Cu2(P,P\\u2032-diphenylmethylenediphosphinate)24,4\\u2032-bipyridine\\n\",\n        \"output\": \" Cu2(PCP)2BIPY\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Hf6O6(OH)2(2,5-thiophenedicarboxylate)4.5\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(2,5-thiophenedicarboxylate)5\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" H3(Cu4Cl)3(1,3,5-tris(1H-1,2,3-triazol-5-yl)benzene)8\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Al(OH)(1,4-benzenedicarboxylate-F)\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn(2-((pyridin-4-yl)methylamino)-4-methylpentanoate4)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate5)\\n\",\n        \"output\": \" Zn(L14)(L15)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn4O(2,2\\u2032-bis-trifluoromethyl-biphenyl-4,4\\u2032-dicarboxylate)3(4,4\\u2032-bipyridine)0.5(H2O)\\n\",\n        \"output\": \" Zn4O(BFBPDC)3(BPY)0.5(H2O)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Cu2(2\\u2032,5\\u2032-dialkyloxy-[1,1\\u2032:4\\u2032,1\\u2033-terphenyl]-3,3\\u2033,5,5\\u2033-tetracarboxylate-(n-hexyl))\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-(CH3)2)3\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" La(3,5-bis(2H-tetrazol-5-yl)-benzoate)H2O\\n\",\n        \"output\": \" La(BTB)H2O\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" america\\n\",\n        \"output\": \" america has no activated formula unit.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn(2-Aminopropanoate)(OAc)\\n\",\n        \"output\": \" Zn(Ala)(OAc)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Al(OH)(1,4-benzenedicarboxylate)\\n\",\n        \"output\": \" Al(OH)(BDC)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at normal measurement conditions? ->\",\n        \"input\": \" Hf6O6(OH)2(dithieno[3,2-b;2\\u2032,3\\u2032-d]-thiophene-2,6-dicarboxylate)4\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Al12O(OH)18(H2O)3(Al2(OH)4)(1,3,5-benzenetricarboxylate)6\\n\",\n        \"output\": \" Al12O(OH)18(H2O)3(Al2(OH)4)(BTC)6\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Co2(1,4-benzenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \" Co2(BDC)2(DABCO)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn(2-Amino-3-methylbutanoic acid)(Cl)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Cd(2,6-napthalenedicarboxylate)0.5(PCA)\\n\",\n        \"output\": \" Cd(2,6-NDC)0.5(PCA)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" EuCu(Pyridine-3-carboxylate)2(oxalate)\\n\",\n        \"output\": \" EuCu(NIC)2(C2O4)\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn(phenyl benzimidazolate)2\\n\",\n        \"output\": \" Zn(PhIM)2\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Cu3(1,3,5-benzenetricarboxylate-CH3)2(H2O)3\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(1,3,5-benzenetricarboxylate)2(HCOO)6\\n\",\n        \"output\": \" Zr6O4(OH)4(BTC)2(HCOO)6\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(1,4-benzenedicarboxylate-(OH)2)6\\n\",\n        \"output\": \" Zr6O4(OH)4(BDC-(OH)2)6\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zn(1,4-benzenedi(4-pyrazolyl))\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" ZrO(1,4-benzenedicarboxylate)\\n\",\n        \"output\": \" ZrO(BDC)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn(2-Aminopropanoate)(OAc)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cu(4,4\\u2032-hexafluoroisopropylidene-bis-benzoate)(H24,4\\u2032-hexafluoroisopropylidene-bis-benzoate)0.5\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn2(1,4-napthalenedicarboxylate)2(4-diazabicyclo[2.2.2]-octane)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Co(2-((pyridin-4-yl)methylamino)-4-methylpentanoate3)2\\n\",\n        \"output\": \" Co(L13)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(4,4\\u2032,4\\u2033,4\\u2034-methanetetrayltetrabenzoate)2(HCOO)4(H2O)4\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Co2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Ni2(oxalate)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate6)2\\n\",\n        \"output\": \" Ni2(C2O4)(L16)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn(2-Amino-3-methylbutanoic acid)(Cl)\\n\",\n        \"output\": \" Zn(VAL)(Cl)\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O4(OH)4(OH)4(H2O)4(Mmeso-tetra(4-carboxyl-phenyl)porphyrin)2\\n\",\n        \"output\": \" Zr6O4(OH)4(OH)4(H2O)4(MTCPP)2\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Ni(2-((pyridin-4-yl)methylamino)-4-methylpentanoate3)2\\n\",\n        \"output\": \" Ni(L13)2\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" CdZrSr(oxalate)4\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-(OMe)2)12\\n\",\n        \"output\": \" Zr6O6(BDC-(OMe)2)12\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" hawk\\n\",\n        \"output\": \" hawk has no water stability.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn2(1,3,5-benzenetricarboxylate)(OH)-(H2O)\\n\",\n        \"output\": \" Zn2(BTC)(OH)-(H2O)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ni2(HFPDPT)-(4,4\\u2032-bipyridine)2(H2O)2](H2O)8\\n\",\n        \"output\": \" Ni2(HFPDPT)-(BPY)2(H2O)2](H2O)8\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-(CO2H)2)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn(1,3-benzenedi(4-pyrazolyl))\\n\",\n        \"output\": \" Zn(1,3-BDP)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-napthalenedicarboxylate)12\\n\",\n        \"output\": \" Zr6O6(1,4-NDC)12\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O4(OH)4(2,6-napthalenedicarboxylate-(OH)2)6\\n\",\n        \"output\": \" Zr6O4(OH)4(2,6-NDC-(OH)2)6\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" [KCo3(2-oxidopropane-1,2,3-tricarboxylate)(2-hydroxypropane-1,2,3-tricarboxylate)(H2O)28H2O]8\\n\",\n        \"output\": \"  It has high water stability with medium confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cd2(2-(pyridin-4-yl)methylamino)-3-hydroxypropanoate)2(Br)2(H2O)3\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ni8(OH)4(H2O)2(2-((pyridin-4-yl)methylamino)-4-methylpentanoate0-(CF3)2)6\\n\",\n        \"output\": \" Ni8(OH)4(H2O)2(L10-(CF3)2)6\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Cu4(2,2-dimethylpropanoate)8(1,3,5,7-tetrakis(4-(2-ethyl-1H-imidazol-1-yl)phenyl)-ane)\\n\",\n        \"output\": \" Cu4(Me3CCOO)8(TEIA)\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-CH3)12\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ti8O8(OH)4(1,4-benzenedicarboxylate)6\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" V(O)(1,4-benzenedicarboxylate-F)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-(CH3)2)3\\n\",\n        \"output\": \" Zn4O(BDC-(CH3)2)3\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-NH2)12\\n\",\n        \"output\": \" Zr6O6(BDC-NH2)12\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn2(2,6-napthalenedicarboxylate)2(4,4\\u2032-bipyridine)\\n\",\n        \"output\": \" Zn2(2,6-NDC)2(BPY)\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn3(2,3,5-Triphenyltetrazolium chloride)(OH)2(H2O)\\n\",\n        \"output\": \" Zn3(TTC)(OH)2(H2O)\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zn(ICA)2\\n\",\n        \"output\": \" Zn(ICA)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Ni2(oxalate)(2-((pyridin-4-yl)methylamino)-4-methylpentanoate6)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" Cu2(2\\u2032,5\\u2032-dialkyloxy-[1,1\\u2032:4\\u2032,1\\u2033-terphenyl]-3,3\\u2033,5,5\\u2033-tetracarboxylate-(ethyl))\\n\",\n        \"output\": \" Cu2(TPTC-O-(ethyl))\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zr6O8(H2O)8(meso-tetra(4-carboxyl-phenyl)porphyrin-H2)2\\n\",\n        \"output\": \" Zr6O8(H2O)8(TCPP-H2)2\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O4(OH)4(1,4-benzenedicarboxylate-(OH)2)6\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn2(2,5-dihydroxyterephthalate)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O4(OH)4(meso-tetra(4-carboxyl-phenyl)porphyrin-H2)3\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Hf6O6(OH)2(2,5-thiophenedicarboxylate)4\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Ni-(1,2-bis(4-pyridyl)ethane)2(MoO4)\\n\",\n        \"output\": \" Ni-(BPE)2(MoO4)\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cu4(2,2-dimethylpropanoate)8(1,3,5,7-tetrakis(4-(2-ethyl-1H-imidazol-1-yl)phenyl)-ane)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-NH2)12\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"What is activated formula unit of given name? ->\",\n        \"input\": \" Zr3O2(OH)2(Tpyridine-2,4-dicarboxylate-(CH3)4)3\\n\",\n        \"output\": \" Zr3O2(OH)2(TPDC-(CH3)4)3\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Cu3(biphenyl-3,4\\u2032,5-tricarboxylate)\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me activated formula unit of given name. ->\",\n        \"input\": \" [KCo3(2-oxidopropane-1,2,3-tricarboxylate)(2-hydroxypropane-1,2,3-tricarboxylate)(H2O)28H2O]8\\n\",\n        \"output\": \" [KCo3(C6H4O7)(C6H5O7)(H2O)28H2O]8\\n\"\n    },\n    {\n        \"instruction\": \"How is the water stabilityof given stability at room temperature and atmospheric pressure? ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-NH2)3\\n\",\n        \"output\": \"  It has low water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Tell me water stability of given name at normal measurement conditions. ->\",\n        \"input\": \" Zn6(imidazole-4,5-dicarboxylate)4(OH)2(Hpiperazine)2\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Al(OH)(2,6-napthalenedicarboxylate)\\n\",\n        \"output\": \"  It has low water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Write stability of given name at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-CF3)12\\n\",\n        \"output\": \"  It has high water stability with low confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at normal measurement conditions. ->\",\n        \"input\": \" Zr6O6(OH)2(2,5-thiophenedicarboxylate)4\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zn(2-Aminopropanoate)(Cl)\\n\",\n        \"output\": \" Zn(Ala)(Cl)\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-(CH3)2)12\\n\",\n        \"output\": \" Zr6O6(BDC-(CH3)2)12\\n\"\n    },\n    {\n        \"instruction\": \"Write activated formula unit of given name. ->\",\n        \"input\": \" Zn4O(1,4-benzenedicarboxylate-NH2)3\\n\",\n        \"output\": \" Zn4O(BDC-NH2)3\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its water stability at room temperature and atmospheric pressure. ->\",\n        \"input\": \" Zn2(1,4-benzenedicarboxylate)2(4,4\\u2032-bipyridine)\\n\",\n        \"output\": \"  It has high water stability with high confidence.\\n\"\n    },\n    {\n        \"instruction\": \"Given name, write its activated formula unit. ->\",\n        \"input\": \" Zr6O6(1,4-benzenedicarboxylate-F)12\\n\",\n        \"output\": \" Zr6O6(BDC-F)12\\n\"\n    }\n]"
  },
  {
    "path": "evaluate_matbench.py",
    "content": "\r\nimport torch\r\nfrom transformers import LlamaTokenizer, LlamaForCausalLM\r\nimport json\r\nimport argparse \r\nimport re\r\n\r\nparser = argparse.ArgumentParser('Please provide the model path and data path for evaluation')\r\nparser.add_argument('--model_path',type=str,help='model path')\r\nparser.add_argument('--data_path',type=str,help='path of data to be evaluated')\r\nparser.add_argument('--dataset',type=str,help='name of dataset')\r\nparser.add_argument('--fold',type=str,help = 'current fold')\r\nargs = parser.parse_args()\r\n\r\ndef generate_prompt(instruction, input=None):\r\n    if input:\r\n        return f\"\"\"Below is an instruction that describes a task, paired with an input that provides further context. Write a response that appropriately completes the request.\r\n    ### Instruction:\r\n    {instruction}\r\n    ### Input:\r\n    {input}\r\n    ### Response:\"\"\"\r\n    else:\r\n        return f\"\"\"Below is an instruction that describes a task. Write a response that appropriately completes the request.\r\n    ### Instruction:\r\n    {instruction}\r\n    ### Response:\"\"\"\r\n\r\ndef get_first_number(string):\r\n    match = re.match(r'\\d+(\\.\\d+)?', string)\r\n    if match:\r\n        return match.group()\r\n    else:\r\n        return None\r\n\r\nmodel_path = args.model_path\r\ndata_path = args.data_path\r\ndataset = args.dataset\r\nfold = args.fold\r\n\r\ntokenizer = LlamaTokenizer.from_pretrained(model_path)\r\nmodel = LlamaForCausalLM.from_pretrained(\r\n    model_path,\r\n    load_in_8bit=False,\r\n    torch_dtype=torch.float16,\r\n    device_map=\"auto\"\r\n)\r\nmodel.to('cuda')\r\n\r\nprediction = []\r\nwith open(data_path,'r') as f:\r\n    data = json.load(f)\r\nfor i in data:\r\n        text = generate_prompt(i['instruction'],i['input'])\r\n        input_ids= tokenizer(text, return_tensors=\"pt\").input_ids.to(\"cuda\") \r\n        generated_ids = model.generate(\r\n            input_ids, \r\n            max_new_tokens=250, \r\n            do_sample=True, \r\n            repetition_penalty=1.0, \r\n            temperature=0.8, \r\n            top_p=0.75, \r\n            top_k=40\r\n        )\r\n        output = tokenizer.decode(generated_ids[0])\r\n        prediction.append(output)\r\n\r\nwith open(data_path,'r') as f:\r\n    data = json.load(f)\r\n\r\nprocessed_prediction = []\r\nif dataset == 'matbench_expt_is_metal' or dataset == 'matbench_glass':\r\n    for i in range(len(data)):\r\n        if 'Yes' in prediction[i].split('Response: ')[1].split()[0]:\r\n            processed_prediction.append({'input':data[i]['input'],'output':True})\r\n        elif 'No' in prediction[i].split('Response: ')[1].split()[0]:\r\n            processed_prediction.append({'input':data[i]['input'],'output':False})\r\n\r\nelif dataset == 'matbench_steels' or dataset == 'matbench_expt_gap':\r\n    for i in range(len(data)):\r\n        try:\r\n            processed_prediction.append({'input':data[i]['input'],'output':float((get_first_number(prediction[i].split('Response: ')[1].split()[0])))})\r\n        except:\r\n            processed_prediction.append({'input':data[i]['input'],'output':0.00})\r\n        \r\n\r\nwith open('matbench_base_fold_'+str(fold)+'_'+dataset+'_test_result.json','w')as f:\r\n    json.dump(processed_prediction,f)\r\n\r\n"
  },
  {
    "path": "example.ipynb",
    "content": "{\n \"cells\": [\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 2,\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"import torch\\n\",\n    \"from transformers import LlamaTokenizer, LlamaForCausalLM\\n\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 3,\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"loading model, path: darwin/mix_training2\\n\"\n     ]\n    },\n    {\n     \"data\": {\n      \"application/vnd.jupyter.widget-view+json\": {\n       \"model_id\": \"ad9276358c094ba89cae00cbd314226c\",\n       \"version_major\": 2,\n       \"version_minor\": 0\n      },\n      \"text/plain\": [\n       \"Loading checkpoint shards:   0%|          | 0/3 [00:00<?, ?it/s]\"\n      ]\n     },\n     \"metadata\": {},\n     \"output_type\": \"display_data\"\n    }\n   ],\n   \"source\": [\n    \"#load the model\\n\",\n    \"model_path = 'darwin-7B'\\n\",\n    \"print(\\\"loading model, path:\\\", model_path)\\n\",\n    \"tokenizer = LlamaTokenizer.from_pretrained(model_path)\\n\",\n    \"\\n\",\n    \"model = LlamaForCausalLM.from_pretrained(\\n\",\n    \"    model_path,\\n\",\n    \"    load_in_8bit=False,\\n\",\n    \"    torch_dtype=torch.float16,\\n\",\n    \"    device_map=\\\"auto\\\"\\n\",\n    \")\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 4,\n   \"metadata\": {},\n   \"outputs\": [],\n   \"source\": [\n    \"def generate_prompt(instruction, input=None):\\n\",\n    \"    if input:\\n\",\n    \"        return f\\\"\\\"\\\"The following is an instruction that describes a task, paired with an input that provides further context. Write a response that appropriately completes the request.\\n\",\n    \"    ### Instruction:\\n\",\n    \"    {instruction}\\n\",\n    \"    ### Input:\\n\",\n    \"    {input}\\n\",\n    \"    ### Response:\\\"\\\"\\\"\\n\",\n    \"    else:\\n\",\n    \"        return f\\\"\\\"\\\"The following is an instruction that describes a task. Write a response that appropriately completes the request.\\n\",\n    \"    ### Instruction:\\n\",\n    \"    {instruction}\\n\",\n    \"    ### Response:\\\"\\\"\\\"\\n\",\n    \"\\n\",\n    \"def process_response(response):\\n\",\n    \"    response = response.split('Response: ')[1].split('\\\\n')[0]\\n\",\n    \"    return response\\n\",\n    \"\\n\",\n    \"def evaluate(instruction,\\n\",\n    \"             input = None,\\n\",\n    \"             temperature = 0.8,\\n\",\n    \"             top_p = 0.75,\\n\",\n    \"             top_k=40,\\n\",\n    \"             do_sample=True,\\n\",\n    \"             repetition_penalty=1.0,\\n\",\n    \"             max_new_tokens=256,\\n\",\n    \"             **kwargs):\\n\",\n    \"    prompt = generate_prompt(instruction,input)\\n\",\n    \"    input_ids = tokenizer(prompt, return_tensors=\\\"pt\\\").input_ids.to(\\\"cuda\\\")\\n\",\n    \"    generated_ids = model.generate(\\n\",\n    \"        input_ids, \\n\",\n    \"        max_new_tokens=max_new_tokens, \\n\",\n    \"        do_sample=do_sample, \\n\",\n    \"        repetition_penalty=repetition_penalty, \\n\",\n    \"        temperature=temperature, \\n\",\n    \"        top_p=top_p, \\n\",\n    \"        top_k=top_k,\\n\",\n    \"        **kwargs\\n\",\n    \"    )\\n\",\n    \"    response = tokenizer.decode(generated_ids[0])\\n\",\n    \"    response = process_response(response)\\n\",\n    \"    return response\\n\"\n   ]\n  },\n  {\n   \"cell_type\": \"code\",\n   \"execution_count\": 5,\n   \"metadata\": {},\n   \"outputs\": [\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"Instruction: Write lipophilicity of given SMILES. CC(C)C(NC(=O)CN1C(=O)C(=CN=C1C2CCCCC2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\"\n     ]\n    },\n    {\n     \"name\": \"stderr\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"/home/halona/anaconda3/envs/darwin/lib/python3.10/site-packages/transformers/generation/utils.py:1253: UserWarning: You have modified the pretrained model configuration to control generation. This is a deprecated strategy to control generation and will be removed soon, in a future version. Please use a generation configuration file (see https://huggingface.co/docs/transformers/main_classes/text_generation)\\n\",\n      \"  warnings.warn(\\n\"\n     ]\n    },\n    {\n     \"name\": \"stdout\",\n     \"output_type\": \"stream\",\n     \"text\": [\n      \"Response: 2.26\\n\",\n      \"------------------\\n\",\n      \"Instruction: Given compound, write its potential SELFIES. Decalin\\n\",\n      \"Response: [C][C][C][C][C][C][C][C][C][Ring1][Branch1][C][Ring1][=Branch2][C][Ring1][=C][C][Ring1][#Branch2][C][Ring1][=C][C][Ring1][=C][Ring2][Ring1][Ring1][Ring2][Ring1][Ring1][C]\\n\",\n      \"------------------\\n\",\n      \"Instruction: What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? Methyl acrylate\\n\",\n      \"Response: -0.22\\n\",\n      \"------------------\\n\",\n      \"Instruction: Tell me if given composition has glass formation ability. Ni53.5B44C2.5\\n\",\n      \"Response: No, Ni53.5B44C2.5 does not have glass formation ability.\\n\",\n      \"------------------\\n\",\n      \"Instruction: Is composition metal? InSb2S4Cl\\n\",\n      \"Response: No, InSb2S4Cl is not metal.\\n\",\n      \"------------------\\n\"\n     ]\n    }\n   ],\n   \"source\": [\n    \"for instruction in [\\n\",\n    \"    'Write lipophilicity of given SMILES. CC(C)C(NC(=O)CN1C(=O)C(=CN=C1C2CCCCC2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F',\\n\",\n    \"    'Given compound, write its potential SELFIES. Decalin',\\n\",\n    \"    'What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? Methyl acrylate',\\n\",\n    \"    'Tell me if given composition has glass formation ability. Ni53.5B44C2.5',\\n\",\n    \"    'Is composition metal? InSb2S4Cl'\\n\",\n    \"]:\\n\",\n    \"    print(\\\"Instruction:\\\",instruction)\\n\",\n    \"    print('Response:',evaluate(instruction))\\n\",\n    \"    print('------------------')\"\n   ]\n  }\n ],\n \"metadata\": {\n  \"kernelspec\": {\n   \"display_name\": \"darwin\",\n   \"language\": \"python\",\n   \"name\": \"python3\"\n  },\n  \"language_info\": {\n   \"codemirror_mode\": {\n    \"name\": \"ipython\",\n    \"version\": 3\n   },\n   \"file_extension\": \".py\",\n   \"mimetype\": \"text/x-python\",\n   \"name\": \"python\",\n   \"nbconvert_exporter\": \"python\",\n   \"pygments_lexer\": \"ipython3\",\n   \"version\": \"3.10.11\"\n  },\n  \"orig_nbformat\": 4\n },\n \"nbformat\": 4,\n \"nbformat_minor\": 2\n}\n"
  },
  {
    "path": "inference.ipynb",
    "content": "{\n  \"cells\": [\n    {\n      \"cell_type\": \"markdown\",\n      \"metadata\": {\n        \"id\": \"view-in-github\",\n        \"colab_type\": \"text\"\n      },\n      \"source\": [\n        \"<a href=\\\"https://colab.research.google.com/github/MasterAI-EAM/Darwin/blob/main/inference.ipynb\\\" target=\\\"_parent\\\"><img src=\\\"https://colab.research.google.com/assets/colab-badge.svg\\\" alt=\\\"Open In Colab\\\"/></a>\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\"\n        },\n        \"id\": \"TLrkg04aCmpz\",\n        \"outputId\": \"eb34dbad-01cf-457d-deda-8e1dedd9bd8c\"\n      },\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"Cloning into 'Darwin'...\\n\",\n            \"remote: Enumerating objects: 522, done.\\u001b[K\\n\",\n            \"remote: Counting objects: 100% (35/35), done.\\u001b[K\\n\",\n            \"remote: Compressing objects: 100% (27/27), done.\\u001b[K\\n\",\n            \"remote: Total 522 (delta 26), reused 8 (delta 8), pack-reused 487\\u001b[K\\n\",\n            \"Receiving objects: 100% (522/522), 19.73 MiB | 13.77 MiB/s, done.\\n\",\n            \"Resolving deltas: 100% (190/190), done.\\n\"\n          ]\n        }\n      ],\n      \"source\": [\n        \"!git clone https://github.com/MasterAI-EAM/Darwin.git\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\"\n        },\n        \"id\": \"IEJsRip9Dhpb\",\n        \"outputId\": \"376862f6-d73a-46a1-c6af-c846ab98430d\"\n      },\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"Requirement already satisfied: numpy in /usr/local/lib/python3.10/dist-packages (from -r Darwin/requirements.txt (line 1)) (1.23.5)\\n\",\n            \"Collecting rouge_score (from -r Darwin/requirements.txt (line 2))\\n\",\n            \"  Downloading rouge_score-0.1.2.tar.gz (17 kB)\\n\",\n            \"  Preparing metadata (setup.py) ... \\u001b[?25l\\u001b[?25hdone\\n\",\n            \"Collecting fire (from -r Darwin/requirements.txt (line 3))\\n\",\n            \"  Downloading fire-0.5.0.tar.gz (88 kB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m88.3/88.3 kB\\u001b[0m \\u001b[31m2.6 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25h  Preparing metadata (setup.py) ... \\u001b[?25l\\u001b[?25hdone\\n\",\n            \"Collecting openai (from -r Darwin/requirements.txt (line 4))\\n\",\n            \"  Downloading openai-0.28.0-py3-none-any.whl (76 kB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m76.5/76.5 kB\\u001b[0m \\u001b[31m4.4 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hCollecting transformers>=4.28.1 (from -r Darwin/requirements.txt (line 5))\\n\",\n            \"  Downloading transformers-4.33.2-py3-none-any.whl (7.6 MB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m7.6/7.6 MB\\u001b[0m \\u001b[31m14.2 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hRequirement already satisfied: torch in /usr/local/lib/python3.10/dist-packages (from -r Darwin/requirements.txt (line 6)) (2.0.1+cu118)\\n\",\n            \"Collecting sentencepiece (from -r Darwin/requirements.txt (line 7))\\n\",\n            \"  Downloading sentencepiece-0.1.99-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl (1.3 MB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m1.3/1.3 MB\\u001b[0m \\u001b[31m12.8 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hCollecting tokenizers>=0.13.3 (from -r Darwin/requirements.txt (line 8))\\n\",\n            \"  Downloading tokenizers-0.14.0-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl (3.8 MB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m3.8/3.8 MB\\u001b[0m \\u001b[31m19.2 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hCollecting wandb (from -r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading wandb-0.15.10-py3-none-any.whl (2.1 MB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m2.1/2.1 MB\\u001b[0m \\u001b[31m17.4 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hRequirement already satisfied: absl-py in /usr/local/lib/python3.10/dist-packages (from rouge_score->-r Darwin/requirements.txt (line 2)) (1.4.0)\\n\",\n            \"Requirement already satisfied: nltk in /usr/local/lib/python3.10/dist-packages (from rouge_score->-r Darwin/requirements.txt (line 2)) (3.8.1)\\n\",\n            \"Requirement already satisfied: six>=1.14.0 in /usr/local/lib/python3.10/dist-packages (from rouge_score->-r Darwin/requirements.txt (line 2)) (1.16.0)\\n\",\n            \"Requirement already satisfied: termcolor in /usr/local/lib/python3.10/dist-packages (from fire->-r Darwin/requirements.txt (line 3)) (2.3.0)\\n\",\n            \"Requirement already satisfied: requests>=2.20 in /usr/local/lib/python3.10/dist-packages (from openai->-r Darwin/requirements.txt (line 4)) (2.31.0)\\n\",\n            \"Requirement already satisfied: tqdm in /usr/local/lib/python3.10/dist-packages (from openai->-r Darwin/requirements.txt (line 4)) (4.66.1)\\n\",\n            \"Requirement already satisfied: aiohttp in /usr/local/lib/python3.10/dist-packages (from openai->-r Darwin/requirements.txt (line 4)) (3.8.5)\\n\",\n            \"Requirement already satisfied: filelock in /usr/local/lib/python3.10/dist-packages (from transformers>=4.28.1->-r Darwin/requirements.txt (line 5)) (3.12.2)\\n\",\n            \"Collecting huggingface-hub<1.0,>=0.15.1 (from transformers>=4.28.1->-r Darwin/requirements.txt (line 5))\\n\",\n            \"  Downloading huggingface_hub-0.17.2-py3-none-any.whl (294 kB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m294.9/294.9 kB\\u001b[0m \\u001b[31m13.9 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hRequirement already satisfied: packaging>=20.0 in /usr/local/lib/python3.10/dist-packages (from transformers>=4.28.1->-r Darwin/requirements.txt (line 5)) (23.1)\\n\",\n            \"Requirement already satisfied: pyyaml>=5.1 in /usr/local/lib/python3.10/dist-packages (from transformers>=4.28.1->-r Darwin/requirements.txt (line 5)) (6.0.1)\\n\",\n            \"Requirement already satisfied: regex!=2019.12.17 in /usr/local/lib/python3.10/dist-packages (from transformers>=4.28.1->-r Darwin/requirements.txt (line 5)) (2023.6.3)\\n\",\n            \"Collecting tokenizers>=0.13.3 (from -r Darwin/requirements.txt (line 8))\\n\",\n            \"  Downloading tokenizers-0.13.3-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl (7.8 MB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m7.8/7.8 MB\\u001b[0m \\u001b[31m15.8 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hCollecting safetensors>=0.3.1 (from transformers>=4.28.1->-r Darwin/requirements.txt (line 5))\\n\",\n            \"  Downloading safetensors-0.3.3-cp310-cp310-manylinux_2_17_x86_64.manylinux2014_x86_64.whl (1.3 MB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m1.3/1.3 MB\\u001b[0m \\u001b[31m15.5 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hRequirement already satisfied: typing-extensions in /usr/local/lib/python3.10/dist-packages (from torch->-r Darwin/requirements.txt (line 6)) (4.5.0)\\n\",\n            \"Requirement already satisfied: sympy in /usr/local/lib/python3.10/dist-packages (from torch->-r Darwin/requirements.txt (line 6)) (1.12)\\n\",\n            \"Requirement already satisfied: networkx in /usr/local/lib/python3.10/dist-packages (from torch->-r Darwin/requirements.txt (line 6)) (3.1)\\n\",\n            \"Requirement already satisfied: jinja2 in /usr/local/lib/python3.10/dist-packages (from torch->-r Darwin/requirements.txt (line 6)) (3.1.2)\\n\",\n            \"Requirement already satisfied: triton==2.0.0 in /usr/local/lib/python3.10/dist-packages (from torch->-r Darwin/requirements.txt (line 6)) (2.0.0)\\n\",\n            \"Requirement already satisfied: cmake in /usr/local/lib/python3.10/dist-packages (from triton==2.0.0->torch->-r Darwin/requirements.txt (line 6)) (3.27.4.1)\\n\",\n            \"Requirement already satisfied: lit in /usr/local/lib/python3.10/dist-packages (from triton==2.0.0->torch->-r Darwin/requirements.txt (line 6)) (16.0.6)\\n\",\n            \"Requirement already satisfied: Click!=8.0.0,>=7.1 in /usr/local/lib/python3.10/dist-packages (from wandb->-r Darwin/requirements.txt (line 9)) (8.1.7)\\n\",\n            \"Collecting GitPython!=3.1.29,>=1.0.0 (from wandb->-r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading GitPython-3.1.36-py3-none-any.whl (189 kB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m189.5/189.5 kB\\u001b[0m \\u001b[31m16.0 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hRequirement already satisfied: psutil>=5.0.0 in /usr/local/lib/python3.10/dist-packages (from wandb->-r Darwin/requirements.txt (line 9)) (5.9.5)\\n\",\n            \"Collecting sentry-sdk>=1.0.0 (from wandb->-r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading sentry_sdk-1.31.0-py2.py3-none-any.whl (224 kB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m224.8/224.8 kB\\u001b[0m \\u001b[31m14.6 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hCollecting docker-pycreds>=0.4.0 (from wandb->-r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading docker_pycreds-0.4.0-py2.py3-none-any.whl (9.0 kB)\\n\",\n            \"Collecting pathtools (from wandb->-r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading pathtools-0.1.2.tar.gz (11 kB)\\n\",\n            \"  Preparing metadata (setup.py) ... \\u001b[?25l\\u001b[?25hdone\\n\",\n            \"Collecting setproctitle (from wandb->-r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading setproctitle-1.3.2-cp310-cp310-manylinux_2_5_x86_64.manylinux1_x86_64.manylinux_2_17_x86_64.manylinux2014_x86_64.whl (30 kB)\\n\",\n            \"Requirement already satisfied: setuptools in /usr/local/lib/python3.10/dist-packages (from wandb->-r Darwin/requirements.txt (line 9)) (67.7.2)\\n\",\n            \"Requirement already satisfied: appdirs>=1.4.3 in /usr/local/lib/python3.10/dist-packages (from wandb->-r Darwin/requirements.txt (line 9)) (1.4.4)\\n\",\n            \"Requirement already satisfied: protobuf!=4.21.0,<5,>=3.19.0 in /usr/local/lib/python3.10/dist-packages (from wandb->-r Darwin/requirements.txt (line 9)) (3.20.3)\\n\",\n            \"Collecting gitdb<5,>=4.0.1 (from GitPython!=3.1.29,>=1.0.0->wandb->-r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading gitdb-4.0.10-py3-none-any.whl (62 kB)\\n\",\n            \"\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m62.7/62.7 kB\\u001b[0m \\u001b[31m6.5 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hRequirement already satisfied: fsspec in /usr/local/lib/python3.10/dist-packages (from huggingface-hub<1.0,>=0.15.1->transformers>=4.28.1->-r Darwin/requirements.txt (line 5)) (2023.6.0)\\n\",\n            \"Requirement already satisfied: charset-normalizer<4,>=2 in /usr/local/lib/python3.10/dist-packages (from requests>=2.20->openai->-r Darwin/requirements.txt (line 4)) (3.2.0)\\n\",\n            \"Requirement already satisfied: idna<4,>=2.5 in /usr/local/lib/python3.10/dist-packages (from requests>=2.20->openai->-r Darwin/requirements.txt (line 4)) (3.4)\\n\",\n            \"Requirement already satisfied: urllib3<3,>=1.21.1 in /usr/local/lib/python3.10/dist-packages (from requests>=2.20->openai->-r Darwin/requirements.txt (line 4)) (2.0.4)\\n\",\n            \"Requirement already satisfied: certifi>=2017.4.17 in /usr/local/lib/python3.10/dist-packages (from requests>=2.20->openai->-r Darwin/requirements.txt (line 4)) (2023.7.22)\\n\",\n            \"Requirement already satisfied: attrs>=17.3.0 in /usr/local/lib/python3.10/dist-packages (from aiohttp->openai->-r Darwin/requirements.txt (line 4)) (23.1.0)\\n\",\n            \"Requirement already satisfied: multidict<7.0,>=4.5 in /usr/local/lib/python3.10/dist-packages (from aiohttp->openai->-r Darwin/requirements.txt (line 4)) (6.0.4)\\n\",\n            \"Requirement already satisfied: async-timeout<5.0,>=4.0.0a3 in /usr/local/lib/python3.10/dist-packages (from aiohttp->openai->-r Darwin/requirements.txt (line 4)) (4.0.3)\\n\",\n            \"Requirement already satisfied: yarl<2.0,>=1.0 in /usr/local/lib/python3.10/dist-packages (from aiohttp->openai->-r Darwin/requirements.txt (line 4)) (1.9.2)\\n\",\n            \"Requirement already satisfied: frozenlist>=1.1.1 in /usr/local/lib/python3.10/dist-packages (from aiohttp->openai->-r Darwin/requirements.txt (line 4)) (1.4.0)\\n\",\n            \"Requirement already satisfied: aiosignal>=1.1.2 in /usr/local/lib/python3.10/dist-packages (from aiohttp->openai->-r Darwin/requirements.txt (line 4)) (1.3.1)\\n\",\n            \"Requirement already satisfied: MarkupSafe>=2.0 in /usr/local/lib/python3.10/dist-packages (from jinja2->torch->-r Darwin/requirements.txt (line 6)) (2.1.3)\\n\",\n            \"Requirement already satisfied: joblib in /usr/local/lib/python3.10/dist-packages (from nltk->rouge_score->-r Darwin/requirements.txt (line 2)) (1.3.2)\\n\",\n            \"Requirement already satisfied: mpmath>=0.19 in /usr/local/lib/python3.10/dist-packages (from sympy->torch->-r Darwin/requirements.txt (line 6)) (1.3.0)\\n\",\n            \"Collecting smmap<6,>=3.0.1 (from gitdb<5,>=4.0.1->GitPython!=3.1.29,>=1.0.0->wandb->-r Darwin/requirements.txt (line 9))\\n\",\n            \"  Downloading smmap-5.0.1-py3-none-any.whl (24 kB)\\n\",\n            \"Building wheels for collected packages: rouge_score, fire, pathtools\\n\",\n            \"  Building wheel for rouge_score (setup.py) ... \\u001b[?25l\\u001b[?25hdone\\n\",\n            \"  Created wheel for rouge_score: filename=rouge_score-0.1.2-py3-none-any.whl size=24932 sha256=e68f11d6464411abb97a285da653419e01c65ee0bf00e0323a024d844316e349\\n\",\n            \"  Stored in directory: /root/.cache/pip/wheels/5f/dd/89/461065a73be61a532ff8599a28e9beef17985c9e9c31e541b4\\n\",\n            \"  Building wheel for fire (setup.py) ... \\u001b[?25l\\u001b[?25hdone\\n\",\n            \"  Created wheel for fire: filename=fire-0.5.0-py2.py3-none-any.whl size=116934 sha256=162db7e1973d4593abb1a35a6f9fb9b99af4f4717cb0b35cb2d1ee0577f9417d\\n\",\n            \"  Stored in directory: /root/.cache/pip/wheels/90/d4/f7/9404e5db0116bd4d43e5666eaa3e70ab53723e1e3ea40c9a95\\n\",\n            \"  Building wheel for pathtools (setup.py) ... \\u001b[?25l\\u001b[?25hdone\\n\",\n            \"  Created wheel for pathtools: filename=pathtools-0.1.2-py3-none-any.whl size=8791 sha256=ed0f9816b4d534561201099a4c415f02df0094614b1cf8389cf975c88c2e26b9\\n\",\n            \"  Stored in directory: /root/.cache/pip/wheels/e7/f3/22/152153d6eb222ee7a56ff8617d80ee5207207a8c00a7aab794\\n\",\n            \"Successfully built rouge_score fire pathtools\\n\",\n            \"Installing collected packages: tokenizers, sentencepiece, safetensors, pathtools, smmap, setproctitle, sentry-sdk, fire, docker-pycreds, rouge_score, huggingface-hub, gitdb, transformers, openai, GitPython, wandb\\n\",\n            \"Successfully installed GitPython-3.1.36 docker-pycreds-0.4.0 fire-0.5.0 gitdb-4.0.10 huggingface-hub-0.17.2 openai-0.28.0 pathtools-0.1.2 rouge_score-0.1.2 safetensors-0.3.3 sentencepiece-0.1.99 sentry-sdk-1.31.0 setproctitle-1.3.2 smmap-5.0.1 tokenizers-0.13.3 transformers-4.33.2 wandb-0.15.10\\n\"\n          ]\n        }\n      ],\n      \"source\": [\n        \"!pip install -r Darwin/requirements.txt\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"id\": \"39yN-dTDffbg\",\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\"\n        },\n        \"outputId\": \"2a9ba7ed-ab49-4549-c1ff-d492344402bb\"\n      },\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"cpu\\n\"\n          ]\n        }\n      ],\n      \"source\": [\n        \"import torch\\n\",\n        \"from transformers import LlamaTokenizer, LlamaForCausalLM\\n\",\n        \"if torch.cuda.is_available():\\n\",\n        \"  device = torch.device(\\\"cuda\\\")\\n\",\n        \"else:\\n\",\n        \"  device = torch.device(\\\"cpu\\\")\\n\",\n        \"print(device)\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\"\n        },\n        \"id\": \"rLsDM0Kbf_uz\",\n        \"outputId\": \"afb5457e-4531-47f1-cd67-0b5af0a55b65\"\n      },\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"Collecting accelerate\\n\",\n            \"  Downloading accelerate-0.23.0-py3-none-any.whl (258 kB)\\n\",\n            \"\\u001b[?25l     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m0.0/258.1 kB\\u001b[0m \\u001b[31m?\\u001b[0m eta \\u001b[36m-:--:--\\u001b[0m\\r\\u001b[2K     \\u001b[91m━━━━━━━━━━━━━━━━━\\u001b[0m\\u001b[90m╺\\u001b[0m\\u001b[90m━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m112.6/258.1 kB\\u001b[0m \\u001b[31m3.2 MB/s\\u001b[0m eta \\u001b[36m0:00:01\\u001b[0m\\r\\u001b[2K     \\u001b[90m━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━\\u001b[0m \\u001b[32m258.1/258.1 kB\\u001b[0m \\u001b[31m4.7 MB/s\\u001b[0m eta \\u001b[36m0:00:00\\u001b[0m\\n\",\n            \"\\u001b[?25hRequirement already satisfied: numpy>=1.17 in /usr/local/lib/python3.10/dist-packages (from accelerate) (1.23.5)\\n\",\n            \"Requirement already satisfied: packaging>=20.0 in /usr/local/lib/python3.10/dist-packages (from accelerate) (23.1)\\n\",\n            \"Requirement already satisfied: psutil in /usr/local/lib/python3.10/dist-packages (from accelerate) (5.9.5)\\n\",\n            \"Requirement already satisfied: pyyaml in /usr/local/lib/python3.10/dist-packages (from accelerate) (6.0.1)\\n\",\n            \"Requirement already satisfied: torch>=1.10.0 in /usr/local/lib/python3.10/dist-packages (from accelerate) (2.0.1+cu118)\\n\",\n            \"Requirement already satisfied: huggingface-hub in /usr/local/lib/python3.10/dist-packages (from accelerate) (0.17.2)\\n\",\n            \"Requirement already satisfied: filelock in /usr/local/lib/python3.10/dist-packages (from torch>=1.10.0->accelerate) (3.12.2)\\n\",\n            \"Requirement already satisfied: typing-extensions in /usr/local/lib/python3.10/dist-packages (from torch>=1.10.0->accelerate) (4.5.0)\\n\",\n            \"Requirement already satisfied: sympy in /usr/local/lib/python3.10/dist-packages (from torch>=1.10.0->accelerate) (1.12)\\n\",\n            \"Requirement already satisfied: networkx in /usr/local/lib/python3.10/dist-packages (from torch>=1.10.0->accelerate) (3.1)\\n\",\n            \"Requirement already satisfied: jinja2 in /usr/local/lib/python3.10/dist-packages (from torch>=1.10.0->accelerate) (3.1.2)\\n\",\n            \"Requirement already satisfied: triton==2.0.0 in /usr/local/lib/python3.10/dist-packages (from torch>=1.10.0->accelerate) (2.0.0)\\n\",\n            \"Requirement already satisfied: cmake in /usr/local/lib/python3.10/dist-packages (from triton==2.0.0->torch>=1.10.0->accelerate) (3.27.4.1)\\n\",\n            \"Requirement already satisfied: lit in /usr/local/lib/python3.10/dist-packages (from triton==2.0.0->torch>=1.10.0->accelerate) (16.0.6)\\n\",\n            \"Requirement already satisfied: fsspec in /usr/local/lib/python3.10/dist-packages (from huggingface-hub->accelerate) (2023.6.0)\\n\",\n            \"Requirement already satisfied: requests in /usr/local/lib/python3.10/dist-packages (from huggingface-hub->accelerate) (2.31.0)\\n\",\n            \"Requirement already satisfied: tqdm>=4.42.1 in /usr/local/lib/python3.10/dist-packages (from huggingface-hub->accelerate) (4.66.1)\\n\",\n            \"Requirement already satisfied: MarkupSafe>=2.0 in /usr/local/lib/python3.10/dist-packages (from jinja2->torch>=1.10.0->accelerate) (2.1.3)\\n\",\n            \"Requirement already satisfied: charset-normalizer<4,>=2 in /usr/local/lib/python3.10/dist-packages (from requests->huggingface-hub->accelerate) (3.2.0)\\n\",\n            \"Requirement already satisfied: idna<4,>=2.5 in /usr/local/lib/python3.10/dist-packages (from requests->huggingface-hub->accelerate) (3.4)\\n\",\n            \"Requirement already satisfied: urllib3<3,>=1.21.1 in /usr/local/lib/python3.10/dist-packages (from requests->huggingface-hub->accelerate) (2.0.4)\\n\",\n            \"Requirement already satisfied: certifi>=2017.4.17 in /usr/local/lib/python3.10/dist-packages (from requests->huggingface-hub->accelerate) (2023.7.22)\\n\",\n            \"Requirement already satisfied: mpmath>=0.19 in /usr/local/lib/python3.10/dist-packages (from sympy->torch>=1.10.0->accelerate) (1.3.0)\\n\",\n            \"Installing collected packages: accelerate\\n\",\n            \"Successfully installed accelerate-0.23.0\\n\"\n          ]\n        }\n      ],\n      \"source\": [\n        \"!pip install accelerate\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\"\n        },\n        \"id\": \"nkfFUwNrMZ8w\",\n        \"outputId\": \"9d600f22-2036-493d-e1f5-675e9694f4f0\"\n      },\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"Access denied with the following error:\\n\",\n            \"\\n\",\n            \" \\tToo many users have viewed or downloaded this file recently. Please\\n\",\n            \"\\ttry accessing the file again later. If the file you are trying to\\n\",\n            \"\\taccess is particularly large or is shared with many people, it may\\n\",\n            \"\\ttake up to 24 hours to be able to view or download the file. If you\\n\",\n            \"\\tstill can't access a file after 24 hours, contact your domain\\n\",\n            \"\\tadministrator. \\n\",\n            \"\\n\",\n            \"You may still be able to access the file from the browser:\\n\",\n            \"\\n\",\n            \"\\t https://drive.google.com/uc?id=1LdzCrbDxxUgT6udB87QmTTEZYs5ZN_EE \\n\",\n            \"\\n\"\n          ]\n        }\n      ],\n      \"source\": [\n        \"!gdown https://drive.google.com/uc?id=1LdzCrbDxxUgT6udB87QmTTEZYs5ZN_EE\\n\",\n        \"\\n\",\n        \"# if Access denied with the following error: Too many users have viewed or downloaded this file recently.\\n\",\n        \"# you can manually download this zip file from drive and upload to colab manually.\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"source\": [\n        \"!unzip darwin-7b.zip\"\n      ],\n      \"metadata\": {\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\"\n        },\n        \"id\": \"O61N5i3VdZf6\",\n        \"outputId\": \"85abfc77-dac1-47ce-e23e-43ae129fd0e5\"\n      },\n      \"execution_count\": null,\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"unzip:  cannot find or open darwin-7b.zip, darwin-7b.zip.zip or darwin-7b.zip.ZIP.\\n\"\n          ]\n        }\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\",\n          \"height\": 104,\n          \"referenced_widgets\": [\n            \"c343a0649f834177a37273d3a63ed9cf\",\n            \"0e345c68115143ec833328a7b777ccdd\",\n            \"c743a1e1f60c4bbb9846c7e1a65483ad\",\n            \"39ff0af1e12b445488c8eb4acb914e11\",\n            \"b22c9c03187446ccb52b26bb2ed2d98b\",\n            \"da863f8ad7344de9a1e85d6f5dc7d5a3\",\n            \"5fbf6a87e59e46b5ba68452362fa61e4\",\n            \"8d78d5853c184c96a85689df2012a501\",\n            \"95e77371948e410e9c4734e155fd5ed5\",\n            \"7c4b52dad7494605adbaeb38da38db7a\",\n            \"5c05bd08c2a1442193cefb704a00dacd\"\n          ]\n        },\n        \"id\": \"FoFNNwWyEBNv\",\n        \"outputId\": \"0de1ed22-d064-4c2e-d831-208f7efff653\"\n      },\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stderr\",\n          \"text\": [\n            \"You are using the default legacy behaviour of the <class 'transformers.models.llama.tokenization_llama.LlamaTokenizer'>. If you see this, DO NOT PANIC! This is expected, and simply means that the `legacy` (previous) behavior will be used so nothing changes for you. If you want to use the new behaviour, set `legacy=False`. This should only be set if you understand what it means, and thouroughly read the reason why this was added as explained in https://github.com/huggingface/transformers/pull/24565\\n\"\n          ]\n        },\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"loading model, path: darwin-7b\\n\"\n          ]\n        },\n        {\n          \"output_type\": \"display_data\",\n          \"data\": {\n            \"text/plain\": [\n              \"Loading checkpoint shards:   0%|          | 0/3 [00:00<?, ?it/s]\"\n            ],\n            \"application/vnd.jupyter.widget-view+json\": {\n              \"version_major\": 2,\n              \"version_minor\": 0,\n              \"model_id\": \"c343a0649f834177a37273d3a63ed9cf\"\n            }\n          },\n          \"metadata\": {}\n        }\n      ],\n      \"source\": [\n        \"#load the model\\n\",\n        \"# model_path = 'decapoda-research/llama-7b-hf'\\n\",\n        \"model_path = 'darwin-7b'\\n\",\n        \"print(\\\"loading model, path:\\\", model_path)\\n\",\n        \"tokenizer = LlamaTokenizer.from_pretrained(model_path)\\n\",\n        \"# if you use GPU, usetorch_dtype=torch.float16\\n\",\n        \"# if you use cpu, use torchtype=torch.float32\\n\",\n        \"if device==\\\"cuda\\\":\\n\",\n        \"  torch_type = torch.float16\\n\",\n        \"else:\\n\",\n        \"  torch_type = torch.float32\\n\",\n        \"model = LlamaForCausalLM.from_pretrained(\\n\",\n        \"    model_path,\\n\",\n        \"    load_in_8bit=False,\\n\",\n        \"    torch_dtype=torch_type,\\n\",\n        \"    device_map=\\\"auto\\\"\\n\",\n        \")\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"id\": \"b4j2n3Kgi-qS\"\n      },\n      \"outputs\": [],\n      \"source\": [\n        \"def generate_prompt(instruction, input=None):\\n\",\n        \"    if input:\\n\",\n        \"        return f\\\"\\\"\\\"The following is an instruction that describes a task, paired with an input that provides further context. Write a response that appropriately completes the request.\\n\",\n        \"    ### Instruction:\\n\",\n        \"    {instruction}\\n\",\n        \"    ### Input:\\n\",\n        \"    {input}\\n\",\n        \"    ### Response:\\\"\\\"\\\"\\n\",\n        \"    else:\\n\",\n        \"        return f\\\"\\\"\\\"The following is an instruction that describes a task. Write a response that appropriately completes the request.\\n\",\n        \"    ### Instruction:\\n\",\n        \"    {instruction}\\n\",\n        \"    ### Response:\\\"\\\"\\\"\\n\",\n        \"\\n\",\n        \"def process_response(response):\\n\",\n        \"    response = response.split('Response: ')[1].split('\\\\n')[0]\\n\",\n        \"    return response\\n\",\n        \"\\n\",\n        \"def evaluate(instruction,\\n\",\n        \"       input = None,\\n\",\n        \"       temperature = 0.8,\\n\",\n        \"       top_p = 0.75,\\n\",\n        \"       top_k=40,\\n\",\n        \"       do_sample=True,\\n\",\n        \"       repetition_penalty=1.0,\\n\",\n        \"       max_new_tokens=256,\\n\",\n        \"       **kwargs):\\n\",\n        \"    prompt = generate_prompt(instruction,input)\\n\",\n        \"    # if use gpu, add .to(\\\"cuda\\\")\\n\",\n        \"    input_ids = tokenizer(prompt, return_tensors=\\\"pt\\\").input_ids\\n\",\n        \"    generated_ids = model.generate(\\n\",\n        \"        input_ids,\\n\",\n        \"        max_new_tokens=max_new_tokens,\\n\",\n        \"        do_sample=do_sample,\\n\",\n        \"        repetition_penalty=repetition_penalty,\\n\",\n        \"        temperature=temperature,\\n\",\n        \"        top_p=top_p,\\n\",\n        \"        top_k=top_k,\\n\",\n        \"        **kwargs\\n\",\n        \"    )\\n\",\n        \"    response = tokenizer.decode(generated_ids[0])\\n\",\n        \"    response = process_response(response)\\n\",\n        \"    return response\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"execution_count\": null,\n      \"metadata\": {\n        \"id\": \"Y1naxE58jC2H\",\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\",\n          \"height\": 411\n        },\n        \"outputId\": \"2c637983-d94e-42cd-b8ec-a7a0bae83e86\"\n      },\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"Instruction: Write lipophilicity of given SMILES. CC(C)C(NC(=O)CN1C(=O)C(=CN=C1C2CCCCC2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F\\n\"\n          ]\n        },\n        {\n          \"output_type\": \"error\",\n          \"ename\": \"KeyboardInterrupt\",\n          \"evalue\": \"ignored\",\n          \"traceback\": [\n            \"\\u001b[0;31m---------------------------------------------------------------------------\\u001b[0m\",\n            \"\\u001b[0;31mKeyboardInterrupt\\u001b[0m                         Traceback (most recent call last)\",\n            \"\\u001b[0;32m<ipython-input-8-60e4ef4381a4>\\u001b[0m in \\u001b[0;36m<cell line: 1>\\u001b[0;34m()\\u001b[0m\\n\\u001b[1;32m      7\\u001b[0m ]:\\n\\u001b[1;32m      8\\u001b[0m     \\u001b[0mprint\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m\\\"Instruction:\\\"\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0minstruction\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m----> 9\\u001b[0;31m     \\u001b[0mprint\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m'Response:'\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0mevaluate\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0minstruction\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m     10\\u001b[0m     \\u001b[0mprint\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m'------------------'\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m<ipython-input-6-62b66c8e38e5>\\u001b[0m in \\u001b[0;36mevaluate\\u001b[0;34m(instruction, input, temperature, top_p, top_k, do_sample, repetition_penalty, max_new_tokens, **kwargs)\\u001b[0m\\n\\u001b[1;32m     28\\u001b[0m     \\u001b[0mprompt\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mgenerate_prompt\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0minstruction\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0minput\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m     29\\u001b[0m     \\u001b[0minput_ids\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mtokenizer\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mprompt\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mreturn_tensors\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0;34m\\\"pt\\\"\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0minput_ids\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mto\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m\\\"cuda\\\"\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m---> 30\\u001b[0;31m     generated_ids = model.generate(\\n\\u001b[0m\\u001b[1;32m     31\\u001b[0m         \\u001b[0minput_ids\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m     32\\u001b[0m         \\u001b[0mmax_new_tokens\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mmax_new_tokens\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/torch/utils/_contextlib.py\\u001b[0m in \\u001b[0;36mdecorate_context\\u001b[0;34m(*args, **kwargs)\\u001b[0m\\n\\u001b[1;32m    113\\u001b[0m     \\u001b[0;32mdef\\u001b[0m \\u001b[0mdecorate_context\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    114\\u001b[0m         \\u001b[0;32mwith\\u001b[0m \\u001b[0mctx_factory\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 115\\u001b[0;31m             \\u001b[0;32mreturn\\u001b[0m \\u001b[0mfunc\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    116\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    117\\u001b[0m     \\u001b[0;32mreturn\\u001b[0m \\u001b[0mdecorate_context\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/transformers/generation/utils.py\\u001b[0m in \\u001b[0;36mgenerate\\u001b[0;34m(self, inputs, generation_config, logits_processor, stopping_criteria, prefix_allowed_tokens_fn, synced_gpus, assistant_model, streamer, negative_prompt_ids, negative_prompt_attention_mask, **kwargs)\\u001b[0m\\n\\u001b[1;32m   1646\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1647\\u001b[0m             \\u001b[0;31m# 13. run sample\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m-> 1648\\u001b[0;31m             return self.sample(\\n\\u001b[0m\\u001b[1;32m   1649\\u001b[0m                 \\u001b[0minput_ids\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1650\\u001b[0m                 \\u001b[0mlogits_processor\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mlogits_processor\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/transformers/generation/utils.py\\u001b[0m in \\u001b[0;36msample\\u001b[0;34m(self, input_ids, logits_processor, stopping_criteria, logits_warper, max_length, pad_token_id, eos_token_id, output_attentions, output_hidden_states, output_scores, return_dict_in_generate, synced_gpus, streamer, **model_kwargs)\\u001b[0m\\n\\u001b[1;32m   2728\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   2729\\u001b[0m             \\u001b[0;31m# forward pass to get next token\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m-> 2730\\u001b[0;31m             outputs = self(\\n\\u001b[0m\\u001b[1;32m   2731\\u001b[0m                 \\u001b[0;34m**\\u001b[0m\\u001b[0mmodel_inputs\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   2732\\u001b[0m                 \\u001b[0mreturn_dict\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0;32mTrue\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/torch/nn/modules/module.py\\u001b[0m in \\u001b[0;36m_call_impl\\u001b[0;34m(self, *args, **kwargs)\\u001b[0m\\n\\u001b[1;32m   1499\\u001b[0m                 \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_pre_hooks\\u001b[0m \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_hooks\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1500\\u001b[0m                 or _global_forward_hooks or _global_forward_pre_hooks):\\n\\u001b[0;32m-> 1501\\u001b[0;31m             \\u001b[0;32mreturn\\u001b[0m \\u001b[0mforward_call\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m   1502\\u001b[0m         \\u001b[0;31m# Do not call functions when jit is used\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1503\\u001b[0m         \\u001b[0mfull_backward_hooks\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mnon_full_backward_hooks\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/accelerate/hooks.py\\u001b[0m in \\u001b[0;36mnew_forward\\u001b[0;34m(*args, **kwargs)\\u001b[0m\\n\\u001b[1;32m    163\\u001b[0m                 \\u001b[0moutput\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mold_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    164\\u001b[0m         \\u001b[0;32melse\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 165\\u001b[0;31m             \\u001b[0moutput\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mold_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    166\\u001b[0m         \\u001b[0;32mreturn\\u001b[0m \\u001b[0mmodule\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0m_hf_hook\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mpost_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mmodule\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0moutput\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    167\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/transformers/models/llama/modeling_llama.py\\u001b[0m in \\u001b[0;36mforward\\u001b[0;34m(self, input_ids, attention_mask, position_ids, past_key_values, inputs_embeds, labels, use_cache, output_attentions, output_hidden_states, return_dict)\\u001b[0m\\n\\u001b[1;32m    818\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    819\\u001b[0m         \\u001b[0;31m# decoder outputs consists of (dec_features, layer_state, dec_hidden, dec_attn)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 820\\u001b[0;31m         outputs = self.model(\\n\\u001b[0m\\u001b[1;32m    821\\u001b[0m             \\u001b[0minput_ids\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0minput_ids\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    822\\u001b[0m             \\u001b[0mattention_mask\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mattention_mask\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/torch/nn/modules/module.py\\u001b[0m in \\u001b[0;36m_call_impl\\u001b[0;34m(self, *args, **kwargs)\\u001b[0m\\n\\u001b[1;32m   1499\\u001b[0m                 \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_pre_hooks\\u001b[0m \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_hooks\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1500\\u001b[0m                 or _global_forward_hooks or _global_forward_pre_hooks):\\n\\u001b[0;32m-> 1501\\u001b[0;31m             \\u001b[0;32mreturn\\u001b[0m \\u001b[0mforward_call\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m   1502\\u001b[0m         \\u001b[0;31m# Do not call functions when jit is used\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1503\\u001b[0m         \\u001b[0mfull_backward_hooks\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mnon_full_backward_hooks\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/transformers/models/llama/modeling_llama.py\\u001b[0m in \\u001b[0;36mforward\\u001b[0;34m(self, input_ids, attention_mask, position_ids, past_key_values, inputs_embeds, use_cache, output_attentions, output_hidden_states, return_dict)\\u001b[0m\\n\\u001b[1;32m    706\\u001b[0m                 )\\n\\u001b[1;32m    707\\u001b[0m             \\u001b[0;32melse\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 708\\u001b[0;31m                 layer_outputs = decoder_layer(\\n\\u001b[0m\\u001b[1;32m    709\\u001b[0m                     \\u001b[0mhidden_states\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    710\\u001b[0m                     \\u001b[0mattention_mask\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mattention_mask\\u001b[0m\\u001b[0;34m,\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/torch/nn/modules/module.py\\u001b[0m in \\u001b[0;36m_call_impl\\u001b[0;34m(self, *args, **kwargs)\\u001b[0m\\n\\u001b[1;32m   1499\\u001b[0m                 \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_pre_hooks\\u001b[0m \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_hooks\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1500\\u001b[0m                 or _global_forward_hooks or _global_forward_pre_hooks):\\n\\u001b[0;32m-> 1501\\u001b[0;31m             \\u001b[0;32mreturn\\u001b[0m \\u001b[0mforward_call\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m   1502\\u001b[0m         \\u001b[0;31m# Do not call functions when jit is used\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1503\\u001b[0m         \\u001b[0mfull_backward_hooks\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mnon_full_backward_hooks\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/accelerate/hooks.py\\u001b[0m in \\u001b[0;36mnew_forward\\u001b[0;34m(*args, **kwargs)\\u001b[0m\\n\\u001b[1;32m    163\\u001b[0m                 \\u001b[0moutput\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mold_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    164\\u001b[0m         \\u001b[0;32melse\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 165\\u001b[0;31m             \\u001b[0moutput\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mold_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    166\\u001b[0m         \\u001b[0;32mreturn\\u001b[0m \\u001b[0mmodule\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0m_hf_hook\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mpost_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mmodule\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0moutput\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    167\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/transformers/models/llama/modeling_llama.py\\u001b[0m in \\u001b[0;36mforward\\u001b[0;34m(self, hidden_states, attention_mask, position_ids, past_key_value, output_attentions, use_cache)\\u001b[0m\\n\\u001b[1;32m    435\\u001b[0m         \\u001b[0mresidual\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mhidden_states\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    436\\u001b[0m         \\u001b[0mhidden_states\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mpost_attention_layernorm\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mhidden_states\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 437\\u001b[0;31m         \\u001b[0mhidden_states\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mmlp\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mhidden_states\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    438\\u001b[0m         \\u001b[0mhidden_states\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mresidual\\u001b[0m \\u001b[0;34m+\\u001b[0m \\u001b[0mhidden_states\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    439\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/torch/nn/modules/module.py\\u001b[0m in \\u001b[0;36m_call_impl\\u001b[0;34m(self, *args, **kwargs)\\u001b[0m\\n\\u001b[1;32m   1499\\u001b[0m                 \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_pre_hooks\\u001b[0m \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_hooks\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1500\\u001b[0m                 or _global_forward_hooks or _global_forward_pre_hooks):\\n\\u001b[0;32m-> 1501\\u001b[0;31m             \\u001b[0;32mreturn\\u001b[0m \\u001b[0mforward_call\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m   1502\\u001b[0m         \\u001b[0;31m# Do not call functions when jit is used\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1503\\u001b[0m         \\u001b[0mfull_backward_hooks\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mnon_full_backward_hooks\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/accelerate/hooks.py\\u001b[0m in \\u001b[0;36mnew_forward\\u001b[0;34m(*args, **kwargs)\\u001b[0m\\n\\u001b[1;32m    163\\u001b[0m                 \\u001b[0moutput\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mold_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    164\\u001b[0m         \\u001b[0;32melse\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 165\\u001b[0;31m             \\u001b[0moutput\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mold_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    166\\u001b[0m         \\u001b[0;32mreturn\\u001b[0m \\u001b[0mmodule\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0m_hf_hook\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mpost_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mmodule\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0moutput\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    167\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/transformers/models/llama/modeling_llama.py\\u001b[0m in \\u001b[0;36mforward\\u001b[0;34m(self, x)\\u001b[0m\\n\\u001b[1;32m    218\\u001b[0m             \\u001b[0mdown_proj\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0msum\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mdown_proj\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    219\\u001b[0m         \\u001b[0;32melse\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 220\\u001b[0;31m             \\u001b[0mdown_proj\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mdown_proj\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mact_fn\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mgate_proj\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mx\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m)\\u001b[0m \\u001b[0;34m*\\u001b[0m \\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mup_proj\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mx\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    221\\u001b[0m \\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    222\\u001b[0m         \\u001b[0;32mreturn\\u001b[0m \\u001b[0mdown_proj\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/torch/nn/modules/module.py\\u001b[0m in \\u001b[0;36m_call_impl\\u001b[0;34m(self, *args, **kwargs)\\u001b[0m\\n\\u001b[1;32m   1499\\u001b[0m                 \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_pre_hooks\\u001b[0m \\u001b[0;32mor\\u001b[0m \\u001b[0m_global_backward_hooks\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1500\\u001b[0m                 or _global_forward_hooks or _global_forward_pre_hooks):\\n\\u001b[0;32m-> 1501\\u001b[0;31m             \\u001b[0;32mreturn\\u001b[0m \\u001b[0mforward_call\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m   1502\\u001b[0m         \\u001b[0;31m# Do not call functions when jit is used\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m   1503\\u001b[0m         \\u001b[0mfull_backward_hooks\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mnon_full_backward_hooks\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m[\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/accelerate/hooks.py\\u001b[0m in \\u001b[0;36mnew_forward\\u001b[0;34m(*args, **kwargs)\\u001b[0m\\n\\u001b[1;32m    158\\u001b[0m     \\u001b[0;34m@\\u001b[0m\\u001b[0mfunctools\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mwraps\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mold_forward\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    159\\u001b[0m     \\u001b[0;32mdef\\u001b[0m \\u001b[0mnew_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 160\\u001b[0;31m         \\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mkwargs\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mmodule\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0m_hf_hook\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mpre_forward\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mmodule\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m*\\u001b[0m\\u001b[0margs\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m**\\u001b[0m\\u001b[0mkwargs\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    161\\u001b[0m         \\u001b[0;32mif\\u001b[0m \\u001b[0mmodule\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0m_hf_hook\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mno_grad\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    162\\u001b[0m             \\u001b[0;32mwith\\u001b[0m \\u001b[0mtorch\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mno_grad\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/accelerate/hooks.py\\u001b[0m in \\u001b[0;36mpre_forward\\u001b[0;34m(self, module, *args, **kwargs)\\u001b[0m\\n\\u001b[1;32m    284\\u001b[0m                     \\u001b[0;32mif\\u001b[0m \\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mweights_map\\u001b[0m\\u001b[0;34m[\\u001b[0m\\u001b[0mname\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mdtype\\u001b[0m \\u001b[0;34m==\\u001b[0m \\u001b[0mtorch\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mint8\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    285\\u001b[0m                         \\u001b[0mfp16_statistics\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mweights_map\\u001b[0m\\u001b[0;34m[\\u001b[0m\\u001b[0mname\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mreplace\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0;34m\\\"weight\\\"\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0;34m\\\"SCB\\\"\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 286\\u001b[0;31m                 set_module_tensor_to_device(\\n\\u001b[0m\\u001b[1;32m    287\\u001b[0m                     \\u001b[0mmodule\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mname\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mexecution_device\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mvalue\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mself\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mweights_map\\u001b[0m\\u001b[0;34m[\\u001b[0m\\u001b[0mname\\u001b[0m\\u001b[0;34m]\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mfp16_statistics\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mfp16_statistics\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    288\\u001b[0m                 )\\n\",\n            \"\\u001b[0;32m/usr/local/lib/python3.10/dist-packages/accelerate/utils/modeling.py\\u001b[0m in \\u001b[0;36mset_module_tensor_to_device\\u001b[0;34m(module, tensor_name, device, value, dtype, fp16_statistics)\\u001b[0m\\n\\u001b[1;32m    315\\u001b[0m                     \\u001b[0mmodule\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0m_parameters\\u001b[0m\\u001b[0;34m[\\u001b[0m\\u001b[0mtensor_name\\u001b[0m\\u001b[0;34m]\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mparam_cls\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mnew_value\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mrequires_grad\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mold_value\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mrequires_grad\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    316\\u001b[0m         \\u001b[0;32melif\\u001b[0m \\u001b[0misinstance\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mvalue\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mtorch\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mTensor\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0;32m--> 317\\u001b[0;31m             \\u001b[0mnew_value\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mvalue\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mto\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mdevice\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[0m\\u001b[1;32m    318\\u001b[0m         \\u001b[0;32melse\\u001b[0m\\u001b[0;34m:\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\\u001b[1;32m    319\\u001b[0m             \\u001b[0mnew_value\\u001b[0m \\u001b[0;34m=\\u001b[0m \\u001b[0mtorch\\u001b[0m\\u001b[0;34m.\\u001b[0m\\u001b[0mtensor\\u001b[0m\\u001b[0;34m(\\u001b[0m\\u001b[0mvalue\\u001b[0m\\u001b[0;34m,\\u001b[0m \\u001b[0mdevice\\u001b[0m\\u001b[0;34m=\\u001b[0m\\u001b[0mdevice\\u001b[0m\\u001b[0;34m)\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0;34m\\u001b[0m\\u001b[0m\\n\",\n            \"\\u001b[0;31mKeyboardInterrupt\\u001b[0m: \"\n          ]\n        }\n      ],\n      \"source\": [\n        \"for instruction in [\\n\",\n        \"    'Write lipophilicity of given SMILES. CC(C)C(NC(=O)CN1C(=O)C(=CN=C1C2CCCCC2)NC(=O)OCc3ccccc3)C(=O)C(F)(F)F',\\n\",\n        \"    'Given compound, write its potential SELFIES. Decalin',\\n\",\n        \"    'What is water solubility expressed as a logarithm in mol/L of given compound in room temperature? Methyl acrylate',\\n\",\n        \"    'Tell me if given composition has glass formation ability. Ni53.5B44C2.5',\\n\",\n        \"    'Is composition metal? InSb2S4Cl'\\n\",\n        \"]:\\n\",\n        \"    print(\\\"Instruction:\\\",instruction)\\n\",\n        \"    print('Response:',evaluate(instruction))\\n\",\n        \"    print('------------------')\"\n      ]\n    },\n    {\n      \"cell_type\": \"code\",\n      \"source\": [\n        \"!ls\\n\",\n        \"!rm -rf darwin-7b\\n\",\n        \"!rm -rf darwin-7b.zip\\n\",\n        \"!rm -rf Darwin\"\n      ],\n      \"metadata\": {\n        \"colab\": {\n          \"base_uri\": \"https://localhost:8080/\"\n        },\n        \"id\": \"rKe0LWUvh0xF\",\n        \"outputId\": \"d4f85eb2-5e09-40b6-b85b-350ad14b5770\"\n      },\n      \"execution_count\": null,\n      \"outputs\": [\n        {\n          \"output_type\": \"stream\",\n          \"name\": \"stdout\",\n          \"text\": [\n            \"Darwin\\tdarwin-7b  darwin-7b.zip  sample_data\\n\"\n          ]\n        }\n      ]\n    }\n  ],\n  \"metadata\": {\n    \"colab\": {\n      \"machine_shape\": \"hm\",\n      \"provenance\": [],\n      \"authorship_tag\": \"ABX9TyMwM2gN+twP1/25aPd2rLUa\",\n      \"include_colab_link\": true\n    },\n    \"kernelspec\": {\n      \"display_name\": \"Python 3\",\n      \"name\": \"python3\"\n    },\n    \"language_info\": {\n      \"name\": \"python\"\n    },\n    \"widgets\": {\n      \"application/vnd.jupyter.widget-state+json\": {\n        \"c343a0649f834177a37273d3a63ed9cf\": {\n          \"model_module\": \"@jupyter-widgets/controls\",\n          \"model_name\": \"HBoxModel\",\n          \"model_module_version\": \"1.5.0\",\n          \"state\": {\n            \"_dom_classes\": [],\n            \"_model_module\": \"@jupyter-widgets/controls\",\n            \"_model_module_version\": \"1.5.0\",\n            \"_model_name\": \"HBoxModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/controls\",\n            \"_view_module_version\": \"1.5.0\",\n            \"_view_name\": \"HBoxView\",\n            \"box_style\": \"\",\n            \"children\": [\n              \"IPY_MODEL_0e345c68115143ec833328a7b777ccdd\",\n              \"IPY_MODEL_c743a1e1f60c4bbb9846c7e1a65483ad\",\n              \"IPY_MODEL_39ff0af1e12b445488c8eb4acb914e11\"\n            ],\n            \"layout\": \"IPY_MODEL_b22c9c03187446ccb52b26bb2ed2d98b\"\n          }\n        },\n        \"0e345c68115143ec833328a7b777ccdd\": {\n          \"model_module\": \"@jupyter-widgets/controls\",\n          \"model_name\": \"HTMLModel\",\n          \"model_module_version\": \"1.5.0\",\n          \"state\": {\n            \"_dom_classes\": [],\n            \"_model_module\": \"@jupyter-widgets/controls\",\n            \"_model_module_version\": \"1.5.0\",\n            \"_model_name\": \"HTMLModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/controls\",\n            \"_view_module_version\": \"1.5.0\",\n            \"_view_name\": \"HTMLView\",\n            \"description\": \"\",\n            \"description_tooltip\": null,\n            \"layout\": \"IPY_MODEL_da863f8ad7344de9a1e85d6f5dc7d5a3\",\n            \"placeholder\": \"​\",\n            \"style\": \"IPY_MODEL_5fbf6a87e59e46b5ba68452362fa61e4\",\n            \"value\": \"Loading checkpoint shards: 100%\"\n          }\n        },\n        \"c743a1e1f60c4bbb9846c7e1a65483ad\": {\n          \"model_module\": \"@jupyter-widgets/controls\",\n          \"model_name\": \"FloatProgressModel\",\n          \"model_module_version\": \"1.5.0\",\n          \"state\": {\n            \"_dom_classes\": [],\n            \"_model_module\": \"@jupyter-widgets/controls\",\n            \"_model_module_version\": \"1.5.0\",\n            \"_model_name\": \"FloatProgressModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/controls\",\n            \"_view_module_version\": \"1.5.0\",\n            \"_view_name\": \"ProgressView\",\n            \"bar_style\": \"success\",\n            \"description\": \"\",\n            \"description_tooltip\": null,\n            \"layout\": \"IPY_MODEL_8d78d5853c184c96a85689df2012a501\",\n            \"max\": 3,\n            \"min\": 0,\n            \"orientation\": \"horizontal\",\n            \"style\": \"IPY_MODEL_95e77371948e410e9c4734e155fd5ed5\",\n            \"value\": 3\n          }\n        },\n        \"39ff0af1e12b445488c8eb4acb914e11\": {\n          \"model_module\": \"@jupyter-widgets/controls\",\n          \"model_name\": \"HTMLModel\",\n          \"model_module_version\": \"1.5.0\",\n          \"state\": {\n            \"_dom_classes\": [],\n            \"_model_module\": \"@jupyter-widgets/controls\",\n            \"_model_module_version\": \"1.5.0\",\n            \"_model_name\": \"HTMLModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/controls\",\n            \"_view_module_version\": \"1.5.0\",\n            \"_view_name\": \"HTMLView\",\n            \"description\": \"\",\n            \"description_tooltip\": null,\n            \"layout\": \"IPY_MODEL_7c4b52dad7494605adbaeb38da38db7a\",\n            \"placeholder\": \"​\",\n            \"style\": \"IPY_MODEL_5c05bd08c2a1442193cefb704a00dacd\",\n            \"value\": \" 3/3 [02:32&lt;00:00, 48.41s/it]\"\n          }\n        },\n        \"b22c9c03187446ccb52b26bb2ed2d98b\": {\n          \"model_module\": \"@jupyter-widgets/base\",\n          \"model_name\": \"LayoutModel\",\n          \"model_module_version\": \"1.2.0\",\n          \"state\": {\n            \"_model_module\": \"@jupyter-widgets/base\",\n            \"_model_module_version\": \"1.2.0\",\n            \"_model_name\": \"LayoutModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/base\",\n            \"_view_module_version\": \"1.2.0\",\n            \"_view_name\": \"LayoutView\",\n            \"align_content\": null,\n            \"align_items\": null,\n            \"align_self\": null,\n            \"border\": null,\n            \"bottom\": null,\n            \"display\": null,\n            \"flex\": null,\n            \"flex_flow\": null,\n            \"grid_area\": null,\n            \"grid_auto_columns\": null,\n            \"grid_auto_flow\": null,\n            \"grid_auto_rows\": null,\n            \"grid_column\": null,\n            \"grid_gap\": null,\n            \"grid_row\": null,\n            \"grid_template_areas\": null,\n            \"grid_template_columns\": null,\n            \"grid_template_rows\": null,\n            \"height\": null,\n            \"justify_content\": null,\n            \"justify_items\": null,\n            \"left\": null,\n            \"margin\": null,\n            \"max_height\": null,\n            \"max_width\": null,\n            \"min_height\": null,\n            \"min_width\": null,\n            \"object_fit\": null,\n            \"object_position\": null,\n            \"order\": null,\n            \"overflow\": null,\n            \"overflow_x\": null,\n            \"overflow_y\": null,\n            \"padding\": null,\n            \"right\": null,\n            \"top\": null,\n            \"visibility\": null,\n            \"width\": null\n          }\n        },\n        \"da863f8ad7344de9a1e85d6f5dc7d5a3\": {\n          \"model_module\": \"@jupyter-widgets/base\",\n          \"model_name\": \"LayoutModel\",\n          \"model_module_version\": \"1.2.0\",\n          \"state\": {\n            \"_model_module\": \"@jupyter-widgets/base\",\n            \"_model_module_version\": \"1.2.0\",\n            \"_model_name\": \"LayoutModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/base\",\n            \"_view_module_version\": \"1.2.0\",\n            \"_view_name\": \"LayoutView\",\n            \"align_content\": null,\n            \"align_items\": null,\n            \"align_self\": null,\n            \"border\": null,\n            \"bottom\": null,\n            \"display\": null,\n            \"flex\": null,\n            \"flex_flow\": null,\n            \"grid_area\": null,\n            \"grid_auto_columns\": null,\n            \"grid_auto_flow\": null,\n            \"grid_auto_rows\": null,\n            \"grid_column\": null,\n            \"grid_gap\": null,\n            \"grid_row\": null,\n            \"grid_template_areas\": null,\n            \"grid_template_columns\": null,\n            \"grid_template_rows\": null,\n            \"height\": null,\n            \"justify_content\": null,\n            \"justify_items\": null,\n            \"left\": null,\n            \"margin\": null,\n            \"max_height\": null,\n            \"max_width\": null,\n            \"min_height\": null,\n            \"min_width\": null,\n            \"object_fit\": null,\n            \"object_position\": null,\n            \"order\": null,\n            \"overflow\": null,\n            \"overflow_x\": null,\n            \"overflow_y\": null,\n            \"padding\": null,\n            \"right\": null,\n            \"top\": null,\n            \"visibility\": null,\n            \"width\": null\n          }\n        },\n        \"5fbf6a87e59e46b5ba68452362fa61e4\": {\n          \"model_module\": \"@jupyter-widgets/controls\",\n          \"model_name\": \"DescriptionStyleModel\",\n          \"model_module_version\": \"1.5.0\",\n          \"state\": {\n            \"_model_module\": \"@jupyter-widgets/controls\",\n            \"_model_module_version\": \"1.5.0\",\n            \"_model_name\": \"DescriptionStyleModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/base\",\n            \"_view_module_version\": \"1.2.0\",\n            \"_view_name\": \"StyleView\",\n            \"description_width\": \"\"\n          }\n        },\n        \"8d78d5853c184c96a85689df2012a501\": {\n          \"model_module\": \"@jupyter-widgets/base\",\n          \"model_name\": \"LayoutModel\",\n          \"model_module_version\": \"1.2.0\",\n          \"state\": {\n            \"_model_module\": \"@jupyter-widgets/base\",\n            \"_model_module_version\": \"1.2.0\",\n            \"_model_name\": \"LayoutModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/base\",\n            \"_view_module_version\": \"1.2.0\",\n            \"_view_name\": \"LayoutView\",\n            \"align_content\": null,\n            \"align_items\": null,\n            \"align_self\": null,\n            \"border\": null,\n            \"bottom\": null,\n            \"display\": null,\n            \"flex\": null,\n            \"flex_flow\": null,\n            \"grid_area\": null,\n            \"grid_auto_columns\": null,\n            \"grid_auto_flow\": null,\n            \"grid_auto_rows\": null,\n            \"grid_column\": null,\n            \"grid_gap\": null,\n            \"grid_row\": null,\n            \"grid_template_areas\": null,\n            \"grid_template_columns\": null,\n            \"grid_template_rows\": null,\n            \"height\": null,\n            \"justify_content\": null,\n            \"justify_items\": null,\n            \"left\": null,\n            \"margin\": null,\n            \"max_height\": null,\n            \"max_width\": null,\n            \"min_height\": null,\n            \"min_width\": null,\n            \"object_fit\": null,\n            \"object_position\": null,\n            \"order\": null,\n            \"overflow\": null,\n            \"overflow_x\": null,\n            \"overflow_y\": null,\n            \"padding\": null,\n            \"right\": null,\n            \"top\": null,\n            \"visibility\": null,\n            \"width\": null\n          }\n        },\n        \"95e77371948e410e9c4734e155fd5ed5\": {\n          \"model_module\": \"@jupyter-widgets/controls\",\n          \"model_name\": \"ProgressStyleModel\",\n          \"model_module_version\": \"1.5.0\",\n          \"state\": {\n            \"_model_module\": \"@jupyter-widgets/controls\",\n            \"_model_module_version\": \"1.5.0\",\n            \"_model_name\": \"ProgressStyleModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/base\",\n            \"_view_module_version\": \"1.2.0\",\n            \"_view_name\": \"StyleView\",\n            \"bar_color\": null,\n            \"description_width\": \"\"\n          }\n        },\n        \"7c4b52dad7494605adbaeb38da38db7a\": {\n          \"model_module\": \"@jupyter-widgets/base\",\n          \"model_name\": \"LayoutModel\",\n          \"model_module_version\": \"1.2.0\",\n          \"state\": {\n            \"_model_module\": \"@jupyter-widgets/base\",\n            \"_model_module_version\": \"1.2.0\",\n            \"_model_name\": \"LayoutModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/base\",\n            \"_view_module_version\": \"1.2.0\",\n            \"_view_name\": \"LayoutView\",\n            \"align_content\": null,\n            \"align_items\": null,\n            \"align_self\": null,\n            \"border\": null,\n            \"bottom\": null,\n            \"display\": null,\n            \"flex\": null,\n            \"flex_flow\": null,\n            \"grid_area\": null,\n            \"grid_auto_columns\": null,\n            \"grid_auto_flow\": null,\n            \"grid_auto_rows\": null,\n            \"grid_column\": null,\n            \"grid_gap\": null,\n            \"grid_row\": null,\n            \"grid_template_areas\": null,\n            \"grid_template_columns\": null,\n            \"grid_template_rows\": null,\n            \"height\": null,\n            \"justify_content\": null,\n            \"justify_items\": null,\n            \"left\": null,\n            \"margin\": null,\n            \"max_height\": null,\n            \"max_width\": null,\n            \"min_height\": null,\n            \"min_width\": null,\n            \"object_fit\": null,\n            \"object_position\": null,\n            \"order\": null,\n            \"overflow\": null,\n            \"overflow_x\": null,\n            \"overflow_y\": null,\n            \"padding\": null,\n            \"right\": null,\n            \"top\": null,\n            \"visibility\": null,\n            \"width\": null\n          }\n        },\n        \"5c05bd08c2a1442193cefb704a00dacd\": {\n          \"model_module\": \"@jupyter-widgets/controls\",\n          \"model_name\": \"DescriptionStyleModel\",\n          \"model_module_version\": \"1.5.0\",\n          \"state\": {\n            \"_model_module\": \"@jupyter-widgets/controls\",\n            \"_model_module_version\": \"1.5.0\",\n            \"_model_name\": \"DescriptionStyleModel\",\n            \"_view_count\": null,\n            \"_view_module\": \"@jupyter-widgets/base\",\n            \"_view_module_version\": \"1.2.0\",\n            \"_view_name\": \"StyleView\",\n            \"description_width\": \"\"\n          }\n        }\n      }\n    }\n  },\n  \"nbformat\": 4,\n  \"nbformat_minor\": 0\n}"
  },
  {
    "path": "inference.py",
    "content": "import torch\r\nfrom transformers import LlamaTokenizer, LlamaForCausalLM\r\nimport sys \r\n\r\n\r\ndef generate_prompt(instruction, input=None):\r\n    if input:\r\n        return f\"\"\"The following is an instruction that describes a task, paired with an input that provides further context. Write a response that appropriately completes the request.\r\n    ### Instruction:\r\n    {instruction}\r\n    ### Input:\r\n    {input}\r\n    ### Response:\"\"\"\r\n    else:\r\n        return f\"\"\"The following is an instruction that describes a task. Write a response that appropriately completes the request.\r\n    ### Instruction:\r\n    {instruction}\r\n    ### Response:\"\"\"\r\n\r\ndef process_response(response):\r\n    response = response.split('Response: ')[1].split('\\n')[0]\r\n    return response\r\n\r\ndef evaluate(instruction,\r\n             input = None,\r\n             temperature = 0.8,\r\n             top_p = 0.75,\r\n             top_k=40,\r\n             do_sample=True,\r\n             repetition_penalty=1.0,\r\n             max_new_tokens=256,\r\n             **kwargs):\r\n    prompt = generate_prompt(instruction,input)\r\n    input_ids = tokenizer(prompt, return_tensors=\"pt\").input_ids.to(\"cuda\")\r\n    generated_ids = model.generate(\r\n        input_ids, \r\n        max_new_tokens=max_new_tokens, \r\n        do_sample=do_sample, \r\n        repetition_penalty=repetition_penalty, \r\n        temperature=temperature, \r\n        top_p=top_p, \r\n        top_k=top_k,\r\n        **kwargs\r\n    )\r\n    response = tokenizer.decode(generated_ids[0])\r\n    response = process_response(response)\r\n    return response\r\n\r\n\r\nmodel_path = str(sys.argv[1])\r\nprint(\"loading model, path:\", model_path)\r\ntokenizer = LlamaTokenizer.from_pretrained(model_path)\r\n\r\nmodel = LlamaForCausalLM.from_pretrained(\r\n    model_path,\r\n    load_in_8bit=False,\r\n    torch_dtype=torch.float16,\r\n    device_map=\"auto\"\r\n)\r\n\r\n\r\nwhile True:\r\n    print('#Response: ',evaluate(input(\"User: \")))\r\n"
  },
  {
    "path": "requirements.txt",
    "content": "numpy\nrouge_score\nfire\nopenai\ntransformers>=4.28.1\ntorch\nsentencepiece\ntokenizers>=0.13.3\nwandb\n"
  },
  {
    "path": "train.py",
    "content": "#    Copyright 2023 Rohan Taori, Ishaan Gulrajani, Tianyi Zhang, Yann Dubois, Xuechen Li\n#\n#    Licensed under the Apache License, Version 2.0 (the \"License\");\n#    you may not use this file except in compliance with the License.\n#    You may obtain a copy of the License at\n#\n#        http://www.apache.org/licenses/LICENSE-2.0\n#\n#    Unless required by applicable law or agreed to in writing, software\n#    distributed under the License is distributed on an \"AS IS\" BASIS,\n#    WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.\n#    See the License for the specific language governing permissions and\n#    limitations under the License.\n\nimport copy\nimport logging\nfrom dataclasses import dataclass, field\nfrom typing import Dict, Optional, Sequence\n\nimport torch\nimport transformers\nimport utils\nfrom torch.utils.data import Dataset\nfrom transformers import Trainer\n\nIGNORE_INDEX = -100\nDEFAULT_PAD_TOKEN = \"[PAD]\"\nDEFAULT_EOS_TOKEN = \"</s>\"\nDEFAULT_BOS_TOKEN = \"<s>\"\nDEFAULT_UNK_TOKEN = \"<unk>\"\nPROMPT_DICT = {\n    \"prompt_input\": (\n        \"Below is an instruction that describes a task, paired with an input that provides further context. \"\n        \"Write a response that appropriately completes the request.\\n\\n\"\n        \"### Instruction:\\n{instruction}\\n\\n### Input:\\n{input}\\n\\n### Response:\"\n    ),\n    \"prompt_no_input\": (\n        \"Below is an instruction that describes a task. \"\n        \"Write a response that appropriately completes the request.\\n\\n\"\n        \"### Instruction:\\n{instruction}\\n\\n### Response:\"\n    ),\n}\n\n\n@dataclass\nclass ModelArguments:\n    model_name_or_path: Optional[str] = field(default=\"facebook/opt-125m\")\n\n\n@dataclass\nclass DataArguments:\n    data_path: str = field(default=None, metadata={\"help\": \"Path to the training data.\"})\n\n\n@dataclass\nclass TrainingArguments(transformers.TrainingArguments):\n    cache_dir: Optional[str] = field(default=None)\n    optim: str = field(default=\"adamw_torch\")\n    n_gpu: int = field(default=1, metadata={\"help\": \"Number of GPUs to use\"})\n    model_max_length: int = field(\n        default=2048,\n        metadata={\"help\": \"Maximum sequence length. Sequences will be right padded (and possibly truncated).\"},\n    )\n\n\ndef smart_tokenizer_and_embedding_resize(\n    special_tokens_dict: Dict,\n    tokenizer: transformers.PreTrainedTokenizer,\n    model: transformers.PreTrainedModel,\n):\n    \"\"\"Resize tokenizer and embedding.\n\n    Note: This is the unoptimized version that may make your embedding size not be divisible by 64.\n    \"\"\"\n    num_new_tokens = tokenizer.add_special_tokens(special_tokens_dict)\n    model.resize_token_embeddings(len(tokenizer))\n\n    if num_new_tokens > 0:\n        input_embeddings = model.get_input_embeddings().weight.data\n        output_embeddings = model.get_output_embeddings().weight.data\n\n        input_embeddings_avg = input_embeddings[:-num_new_tokens].mean(dim=0, keepdim=True)\n        output_embeddings_avg = output_embeddings[:-num_new_tokens].mean(dim=0, keepdim=True)\n\n        input_embeddings[-num_new_tokens:] = input_embeddings_avg\n        output_embeddings[-num_new_tokens:] = output_embeddings_avg\n\n\ndef _tokenize_fn(strings: Sequence[str], tokenizer: transformers.PreTrainedTokenizer) -> Dict:\n    \"\"\"Tokenize a list of strings.\"\"\"\n    tokenized_list = [\n        tokenizer(\n            text,\n            return_tensors=\"pt\",\n            padding=\"longest\",\n            max_length=tokenizer.model_max_length,\n            truncation=True,\n        )\n        for text in strings\n    ]\n    input_ids = labels = [tokenized.input_ids[0] for tokenized in tokenized_list]\n    input_ids_lens = labels_lens = [\n        tokenized.input_ids.ne(tokenizer.pad_token_id).sum().item() for tokenized in tokenized_list\n    ]\n    return dict(\n        input_ids=input_ids,\n        labels=labels,\n        input_ids_lens=input_ids_lens,\n        labels_lens=labels_lens,\n    )\n\n\ndef preprocess(\n    sources: Sequence[str],\n    targets: Sequence[str],\n    tokenizer: transformers.PreTrainedTokenizer,\n) -> Dict:\n    \"\"\"Preprocess the data by tokenizing.\"\"\"\n    examples = [s + t for s, t in zip(sources, targets)]\n    examples_tokenized, sources_tokenized = [_tokenize_fn(strings, tokenizer) for strings in (examples, sources)]\n    input_ids = examples_tokenized[\"input_ids\"]\n    labels = copy.deepcopy(input_ids)\n    for label, source_len in zip(labels, sources_tokenized[\"input_ids_lens\"]):\n        label[:source_len] = IGNORE_INDEX\n    return dict(input_ids=input_ids, labels=labels)\n\n\nclass SupervisedDataset(Dataset):\n    \"\"\"Dataset for supervised fine-tuning.\"\"\"\n\n    def __init__(self, data_path: str, tokenizer: transformers.PreTrainedTokenizer):\n        super(SupervisedDataset, self).__init__()\n        logging.warning(\"Loading data...\")\n        list_data_dict = utils.jload(data_path)\n\n        logging.warning(\"Formatting inputs...\")\n        prompt_input, prompt_no_input = PROMPT_DICT[\"prompt_input\"], PROMPT_DICT[\"prompt_no_input\"]\n        sources = [\n            prompt_input.format_map(example) if example.get(\"input\", \"\") != \"\" else prompt_no_input.format_map(example)\n            for example in list_data_dict\n        ]\n        targets = [f\"{example['output']}{tokenizer.eos_token}\" for example in list_data_dict]\n\n        logging.warning(\"Tokenizing inputs... This may take some time...\")\n        data_dict = preprocess(sources, targets, tokenizer)\n\n        self.input_ids = data_dict[\"input_ids\"]\n        self.labels = data_dict[\"labels\"]\n\n    def __len__(self):\n        return len(self.input_ids)\n\n    def __getitem__(self, i) -> Dict[str, torch.Tensor]:\n        return dict(input_ids=self.input_ids[i], labels=self.labels[i])\n\n\n@dataclass\nclass DataCollatorForSupervisedDataset(object):\n    \"\"\"Collate examples for supervised fine-tuning.\"\"\"\n\n    tokenizer: transformers.PreTrainedTokenizer\n\n    def __call__(self, instances: Sequence[Dict]) -> Dict[str, torch.Tensor]:\n        input_ids, labels = tuple([instance[key] for instance in instances] for key in (\"input_ids\", \"labels\"))\n        input_ids = torch.nn.utils.rnn.pad_sequence(\n            input_ids, batch_first=True, padding_value=self.tokenizer.pad_token_id\n        )\n        labels = torch.nn.utils.rnn.pad_sequence(labels, batch_first=True, padding_value=IGNORE_INDEX)\n        return dict(\n            input_ids=input_ids,\n            labels=labels,\n            attention_mask=input_ids.ne(self.tokenizer.pad_token_id),\n        )\n\n\ndef make_supervised_data_module(tokenizer: transformers.PreTrainedTokenizer, data_args) -> Dict:\n    \"\"\"Make dataset and collator for supervised fine-tuning.\"\"\"\n    train_dataset = SupervisedDataset(tokenizer=tokenizer, data_path=data_args.data_path)\n    data_collator = DataCollatorForSupervisedDataset(tokenizer=tokenizer)\n    return dict(train_dataset=train_dataset, eval_dataset=None, data_collator=data_collator)\n\n\ndef train():\n    parser = transformers.HfArgumentParser((ModelArguments, DataArguments, TrainingArguments))\n    model_args, data_args, training_args = parser.parse_args_into_dataclasses()\n\n    model = transformers.AutoModelForCausalLM.from_pretrained(\n        model_args.model_name_or_path,\n        cache_dir=training_args.cache_dir,\n    )\n\n    tokenizer = transformers.AutoTokenizer.from_pretrained(\n        model_args.model_name_or_path,\n        cache_dir=training_args.cache_dir,\n        model_max_length=training_args.model_max_length,\n        padding_side=\"right\",\n        use_fast=False,\n    )\n    special_tokens_dict = dict()\n    if tokenizer.pad_token is None:\n        special_tokens_dict[\"pad_token\"] = DEFAULT_PAD_TOKEN\n    if tokenizer.eos_token is None:\n        special_tokens_dict[\"eos_token\"] = DEFAULT_EOS_TOKEN\n    if tokenizer.bos_token is None:\n        special_tokens_dict[\"bos_token\"] = DEFAULT_BOS_TOKEN\n    if tokenizer.unk_token is None:\n        special_tokens_dict[\"unk_token\"] = DEFAULT_UNK_TOKEN\n\n    smart_tokenizer_and_embedding_resize(\n        special_tokens_dict=special_tokens_dict,\n        tokenizer=tokenizer,\n        model=model,\n    )\n\n    data_module = make_supervised_data_module(tokenizer=tokenizer, data_args=data_args)\n    trainer = Trainer(model=model, tokenizer=tokenizer, args=training_args, **data_module)\n    trainer.train()\n    trainer.save_state()\n    trainer.save_model(output_dir=training_args.output_dir)\n\n\nif __name__ == \"__main__\":\n    train()\n"
  },
  {
    "path": "utils.py",
    "content": "# -*- coding: utf-8 -*-\r\n# @Time    : 10/12/2023 3:53 PM\r\n# @Author  : WAN Yuwei\r\n# @FileName: utils.py\r\n# @Email: yuweiwan2-c@my.cityu.edu.hk\r\n# @Github: https://github.com/yuweiwan\r\n# @Personal Website: https://yuweiwan.github.io/\r\nimport json\r\nimport io\r\n\r\n\r\ndef _make_r_io_base(f, mode: str):\r\n    if not isinstance(f, io.IOBase):\r\n        f = open(f, mode=mode)\r\n    return f\r\n\r\n\r\ndef jload(f, mode=\"r\"):\r\n    \"\"\"Load a .json file into a dictionary.\"\"\"\r\n    f = _make_r_io_base(f, mode)\r\n    jdict = json.load(f)\r\n    f.close()\r\n    return jdict\r\n"
  }
]